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Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
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We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


1

Method of controlling the mercury vapor pressure in a photo-chemical lamp or vapor filter used for Hg.sup.196 enrichment  

DOE Patents [OSTI]

The present invention is directed to a method of eliminating the cold spot zones presently used on Hg.sup.196 isotope separation lamps and filters by the use of a mercury amalgams, preferably mercury - indium amalgams. The use of an amalgam affords optimization of the mercury density in the lamp and filter of a mercury enrichment reactor, particularly multilamp enrichment reactors. Moreover, the use of an amalgam in such lamps and/or filters affords the ability to control the spectral line width of radiation emitted from lamps, a requirement for mercury enrichment.

Grossman, Mark W. (Belmont, MA)

1993-01-01T23:59:59.000Z

2

Method of controlling the mercury vapor pressure in a photo-chemical lamp or vapor filter used for Hg[sup 196] enrichment  

DOE Patents [OSTI]

The present invention is directed to a method of eliminating the cold spot zones presently used on Hg[sup 196] isotope separation lamps and filters by the use of a mercury amalgams, preferably mercury - indium amalgams. The use of an amalgam affords optimization of the mercury density in the lamp and filter of a mercury enrichment reactor, particularly multilamp enrichment reactors. Moreover, the use of an amalgam in such lamps and/or filters affords the ability to control the spectral line width of radiation emitted from lamps, a requirement for mercury enrichment.

Grossman, M.W.

1993-02-16T23:59:59.000Z

3

Sulfurization of a carbon surface for vapor phase mercury removal II: Sulfur forms and mercury uptake  

E-Print Network [OSTI]

promote the formation of organic sulfur and the presence of H2S during the cooling process increased in the presence of H2S was very effective towards Hg uptake in nitrogen. Corre- lation of mercury uptake capacitySulfurization of a carbon surface for vapor phase mercury removal ­ II: Sulfur forms and mercury

Borguet, Eric

4

Apparatus for isotopic alteration of mercury vapor  

DOE Patents [OSTI]

An apparatus for enriching the isotopic Hg content of mercury is provided. The apparatus includes a reactor, a low pressure electric discharge lamp containing a fill including mercury and an inert gas. A filter is arranged concentrically around the lamp. In a preferred embodiment, constant mercury pressure is maintained in the filter by means of a water-cooled tube that depends from it, the tube having a drop of mercury disposed in it. The reactor is arranged around the filter, whereby radiation from said lamp passes through the filter and into said reactor. The lamp, the filter and the reactor are formed of a material which is transparent to ultraviolet light.

Grossman, Mark W. (Belmont, MA); George, William A. (Gloucester, MA); Marcucci, Rudolph V. (Danvers, MA)

1988-01-01T23:59:59.000Z

5

Filter for isotopic alteration of mercury vapor  

DOE Patents [OSTI]

A filter for enriching the .sup.196 Hg content of mercury, including a reactor, a low pressure electric discharge lamp containing a fill of mercury and an inert gas. A filter is arranged concentrically around the lamp. The reactor is arranged around said filter, whereby radiation from said lamp passes through the filter and into said reactor. The lamp, the filter and the reactor are formed of quartz, and are transparent to ultraviolet light. The .sup.196 Hg concentration in the mercury fill is less than that which is present in naturally occurring mercury, that is less than about 0.146 atomic weight percent. Hydrogen is also included in the fill and serves as a quenching gas in the filter, the hydrogen also serving to prevent disposition of a dark coating on the interior of the filter.

Grossman, Mark W. (Belmont, MA); George, William A. (Gloucestor, MA)

1989-01-01T23:59:59.000Z

6

Filter for isotopic alteration of mercury vapor  

DOE Patents [OSTI]

A filter is described for enriching the [sup 196]Hg content of mercury, including a reactor, a low pressure electric discharge lamp containing a fill of mercury and an inert gas. A filter is arranged concentrically around the lamp. The reactor is arranged around said filter, whereby radiation from said lamp passes through the filter and into said reactor. The lamp, the filter and the reactor are formed of quartz, and are transparent to ultraviolet light. The [sup 196]Hg concentration in the mercury fill is less than that which is present in naturally occurring mercury, that is, less than about 0.146 atomic weight percent. Hydrogen is also included in the fill and serves as a quenching gas in the filter, the hydrogen also serving to prevent disposition of a dark coating on the interior of the filter. 9 figs.

Grossman, M.W.; George, W.A.

1989-06-13T23:59:59.000Z

7

Appendix: Mercury Emissions used in CAM-Chem/Hg model. 1. Anthropogenic emissions  

E-Print Network [OSTI]

Appendix: Mercury Emissions used in CAM-Chem/Hg model. 1. Anthropogenic emissions The anthropogenic emission of mercury is directly adopted from global mercury emission inventory [Pacyna et al., 2005]. The anthropogenic emissions are shown in annual averaged total mercury emissions. (Unit: µg/m2 /day) 2. Land

Meskhidze, Nicholas

8

Mercury Vapor At Lassen Volcanic National Park Area (Varekamp...  

Open Energy Info (EERE)

Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Lassen Volcanic National Park Area (Varekamp & Buseck, 1983) Exploration...

9

Catalytic Reactor For Oxidizing Mercury Vapor  

DOE Patents [OSTI]

A catalytic reactor (10) for oxidizing elemental mercury contained in flue gas is provided. The catalyst reactor (10) comprises within a flue gas conduit a perforated corona discharge plate (30a, b) having a plurality of through openings (33) and a plurality of projecting corona discharge electrodes (31); a perforated electrode plate (40a, b, c) having a plurality of through openings (43) axially aligned with the through openings (33) of the perforated corona discharge plate (30a, b) displaced from and opposing the tips of the corona discharge electrodes (31); and a catalyst member (60a, b, c, d) overlaying that face of the perforated electrode plate (40a, b, c) opposing the tips of the corona discharge electrodes (31). A uniformly distributed corona discharge plasma (1000) is intermittently generated between the plurality of corona discharge electrode tips (31) and the catalyst member (60a, b, c, d) when a stream of flue gas is passed through the conduit. During those periods when corona discharge (1000) is not being generated, the catalyst molecules of the catalyst member (60a, b, c, d) adsorb mercury vapor contained in the passing flue gas. During those periods when corona discharge (1000) is being generated, ions and active radicals contained in the generated corona discharge plasma (1000) desorb the mercury from the catalyst molecules of the catalyst member (60a, b, c, d), oxidizing the mercury in virtually simultaneous manner. The desorption process regenerates and activates the catalyst member molecules.

Helfritch, Dennis J. (Baltimore, MD)

1998-07-28T23:59:59.000Z

10

Application of atomic vapor laser isotope separation to the enrichment of mercury  

SciTech Connect (OSTI)

Workers at GTE/Sylvania have shown that the efficiency of fluorescent lighting may be markedly improved using mercury that has been enriched in the /sup 196/Hg isotope. A 5% improvement in the efficiency of fluorescent lighting in the United States could provide a savings of approx. 1 billion dollars in the corresponding reduction of electrical power consumption. We will discuss the results of recent work done at our laboratory to develop a process for enriching mercury. The discussion will center around the results of spectroscopic measurements of excited state lifetimes, photoionization cross sections and isotope shifts. In addition, we will discuss the mercury separator and supporting laser mesurements of the flow properties of mercury vapor. We will describe the laser system which will provide the photoionization and finally discuss the economic details of producing enriched mercury at a cost that would be attractive to the lighting industry.

Crane, J.K.; Erbert, G.V.; Paisner, J.A.; Chen, H.L.; Chiba, Z.; Beeler, R.G.; Combs, R.; Mostek, S.D.

1986-09-01T23:59:59.000Z

11

Anthropogenic and Natural Emissions of Mercury (Hg) in the northeastern United Jeffrey MacAdam Sigler  

E-Print Network [OSTI]

Abstract Anthropogenic and Natural Emissions of Mercury (Hg) in the northeastern United States impact may depend on the emission rate. Anthropogenic Hg emissions in the United States are poorly characterized. Natural Hg emissions are poorly understood worldwide, due to lack of data or measurement systems

Lee, Xuhui

12

Mercury Absorption in Aqueous Oxidants Catalyzed by Mercury(II) Lynn L. Zhao and Gary T. Rochelle*  

E-Print Network [OSTI]

Mercury Absorption in Aqueous Oxidants Catalyzed by Mercury(II) Lynn L. Zhao and Gary T. Rochelle-1062 The absorption of elemental Hg vapor into aqueous solution containing Hg(II) was measured in a stirred cell at 25 °C. For mercury absorption in Hg(II) obtained by HgCl2 injection, the presence of HNO3 greatly

Rochelle, Gary T.

13

Mercury nonstoichiometry of the Hg1-xBa2CuO4+ superconductor and the P(Hg)-P(O2)-T phase diagram of the Hg-Ba-Cu-O system.  

E-Print Network [OSTI]

1 Mercury nonstoichiometry of the Hg1-xBa2CuO4+ superconductor and the P(Hg)-P(O2)-T phase diagram-nonstoichiometry and exists in a certain P(Hg), P(O2) and T range. Mercury nonstoichiometry of Hg-1201 was investigated in the 923 T 1095 K; 2.0 P(Hg) 8.4 atm; 0.09 P(O2) 0.86 atm ranges. It was found that the mercury

Rudnyi, Evgenii B.

14

Hg L3 XANES Study of Mercury Methylation in Shredded  

E-Print Network [OSTI]

,indicatingbioaccumulationofmercury.Plantsamples collected at this site were also grown in nutrient solution with 1 ppm HgCl2 under (1) aerobic conditions

15

Apparatus and method for removing mercury vapor from a gas stream  

DOE Patents [OSTI]

A metallic filter effectively removes mercury vapor from gas streams. The filter captures the mercury which then can be released and collected as product. The metallic filter is a copper mesh sponge plated with a six micrometer thickness of gold. The filter removes up to 90% of mercury vapor from a mercury contaminated gas stream.

Ganesan, Kumar (Butte, MT)

2008-01-01T23:59:59.000Z

16

The control of mercury vapor using biotrickling filters Ligy Philip a,b,1  

E-Print Network [OSTI]

The control of mercury vapor using biotrickling filters Ligy Philip a,b,1 , Marc A. Deshusses b August 2007 Abstract The feasibility of using biotrickling filters for the removal of mercury vapor from. In particular, the biotrickling filters with sulfur oxidizing bacteria were able to remove 100% of mercury vapor

17

Mercury Lamps Recycling Fluorescent light-tubes, compact fluorescent bulbs, mercury and sodium vapor lamps, ultraviolet and  

E-Print Network [OSTI]

Mercury Lamps Recycling Fluorescent light-tubes, compact fluorescent bulbs, mercury and sodium vapor lamps, ultraviolet and HID (high-intensity discharge) lamps and all other mercury containing labeled for shipment to a recycling plant for mercury, glass and aluminum recovery. The beneficial re

Baker, Chris I.

18

Mother-embryo isotope (15 C) fractionation and mercury (Hg)  

E-Print Network [OSTI]

used to investigate the trophic ecology, foraging habitats and heavy metal contamination). Consequently, Hg concentrations are important to monitor because of the toxicity of this metal. In order of this element in muscle and liver. Key words: sharks; stable isotopes; trace metal; maternal influence. hal

Paris-Sud XI, Université de

19

Vapor phase elemental sulfur amendment for sequestering mercury in contaminated soil  

DOE Patents [OSTI]

The process of treating elemental mercury within the soil is provided by introducing into the soil a heated vapor phase of elemental sulfur. As the vapor phase of elemental sulfur cools, sulfur is precipitated within the soil and then reacts with any elemental mercury thereby producing a reaction product that is less hazardous than elemental mercury.

Looney, Brian B.; Denham, Miles E.; Jackson, Dennis G.

2014-07-08T23:59:59.000Z

20

All mercury lamps contain small amounts of mercury. An electric current passes through the lamp and vaporizes the mercury to generate light. Recycling mercury containing lamps protects human health and our environment from heavy  

E-Print Network [OSTI]

All mercury lamps contain small amounts of mercury. An electric current passes through the lamp and vaporizes the mercury to generate light. Recycling mercury containing lamps protects human health and our the environment by recycling universal wastes, contact EH&S at (949) 824-6200 or visit: www.ehs.uci.edu Mercury

George, Steven C.

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


21

Mercury Vapor (Kooten, 1987) | Open Energy Information  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data CenterFranconia, Virginia: Energy Resources Jump to:46 - 429Lacey,(MonasterLowellisMcDonald isMelletteEnclosed andEnergySolar SystemsVapor

22

High-pressure dissociation of silver mercury iodide, Ag{sub 2}HgI{sub 4}  

SciTech Connect (OSTI)

High-pressure X-ray diffraction has been used to probe the behavior of the superionic conductor silver mercury iodide (Ag{sub 2}HgI{sub 4}) at pressures up to 5GPa and at temperatures from 295 to 370K. Significant changes in the diffraction spectra, indicative of structural transitions, are observed around 0.7 and 1.3GPa across the range of temperatures studied. The change at 0.7GPa is shown to correspond to the dissociation of silver mercury iodide into silver iodide and mercury iodide, i.e., Ag{sub 2}HgI{sub 4}->2AgI+HgI{sub 2}. The second transition, at 1.3GPa, is due to a structural phase transition within HgI{sub 2}. Rietveld analysis of the diffraction data is used to confirm and refine all the known crystal structures.

Parfitt, D.C. [Department of Physics, Oxford University, Parks Road, Oxford OX1 3PU (United Kingdom); Hull, S. [ISIS Facility, Rutherford Appleton Laboratory, Chilton, Didcot, OX11 0QX (United Kingdom)]. E-mail: s.hull@rl.ac.uk; Keen, D.A. [Department of Physics, Oxford University, Parks Road, Oxford OX1 3PU (United Kingdom); ISIS Facility, Rutherford Appleton Laboratory, Chilton, Didcot, OX11 0QX (United Kingdom); Crichton, W. [ESRF, 6 Rue Jules Horowitz, BP 220, 38043 Grenoble CEDEX 9 (France)

2004-10-01T23:59:59.000Z

23

NANOSENSOR DETECTS MERCURY IN WATER J.-S. Lee, M. S. Han, C. A. Mirkin, "Colorimetric Detection of Mercuric Ion (Hg2+  

E-Print Network [OSTI]

NANOSENSOR DETECTS MERCURY IN WATER J.-S. Lee, M. S. Han, C. A. Mirkin, "Colorimetric Detection ­ 0647560 Mercuric ion (Hg2+ ) is one of the most stable inorganic forms of mercury. It is also a caustic

Shull, Kenneth R.

24

An evaluation of elemental mercury vapor exposure to children due to silver-mercury dental amalgam restorations  

E-Print Network [OSTI]

AN EVALUATION OF ELEMENTAL MERCURY VAPOR EXPOSURE TO CHILDREN DUE TO SILVER-MERCURY DENTAL AMALGAM RESTORATIONS A Thesis By RONALD DALE TAYLOR Submitted to the Office of Graduate Studies College Texas A&M University in partial fulfillment.... . . . . 1X LIST OF FIGURES. I. INTRODUCTION. II ' LITERATURE REVIEW Dental Mercury Toxicology Body Burden. Inhalation Exposure. Childhood Exposure III. METHODOLOGY. . . . 3 5 . . . 8 . . . 10 . . . 14 . 16 Human Research Committee...

Taylor, Ronald Dale

1989-01-01T23:59:59.000Z

25

Feasibility of UV lasing without inversion in mercury vapor  

E-Print Network [OSTI]

We investigate the feasibility of UV lasing without inversion at a wavelength of $253.7$ nm utilizing interacting dark resonances in mercury vapor. Our theoretical analysis starts with radiation damped optical Bloch equations for all relevant 13 atomic levels. These master equations are generalized by considering technical phase noise of the driving lasers. From the Doppler broadened complex susceptibility we obtain the stationary output power from semiclassical laser theory. The finite overlap of the driving Gaussian laser beams defines an ellipsoidal inhomogeneous gain distribution. Therefore, we evaluate the intra-cavity field inside a ring laser self-consistently with Fourier optics. This analysis confirms the feasibility of UV lasing and reveals its dependence on experimental parameters.

Martin R. Sturm; Benjamin Rein; Thomas Walther; Reinhold Walser

2014-06-27T23:59:59.000Z

26

Method and apparatus for controlling the flow rate of mercury in a flow system  

DOE Patents [OSTI]

A method for increasing the mercury flow rate to a photochemical mercury enrichment utilizing an entrainment system comprises the steps of passing a carrier gas over a pool of mercury maintained at a first temperature T1, wherein the carrier gas entrains mercury vapor; passing said mercury vapor entrained carrier gas to a second temperature zone T2 having temperature less than T1 to condense said entrained mercury vapor, thereby producing a saturated Hg condition in the carrier gas; and passing said saturated Hg carrier gas to said photochemical enrichment reactor.

Grossman, Mark W. (Belmont, MA); Speer, Richard (Reading, MA)

1991-01-01T23:59:59.000Z

27

Scientific uncertainties in atmospheric mercury models III: Boundary and initial conditions, model grid resolution, and Hg(II) reduction mechanism  

SciTech Connect (OSTI)

In this study, the model response in terms of simulated mercury concentration and deposition to boundary condition (BC), initial condition (IC), model grid resolution (12 km versus 36 km), and two alternative Hg(II) reduction mechanisms, was investigated. The model response to the change of gaseous elemental mercury (GEM) concentration from 0 to 2 ngm3 in IC/BC is found to be very linear (r240.99) based on the results of sensitivity simulations in July 2001. An increase of 1 ngm3 of GEM in BC resulted in an increase of 0.81 ngm3 in the monthly average of total mercury concentration, and 1270 ngm2 in the monthly total deposition. IC has similar but weaker effects compared to those of BC. An increase of 1 ngm3 of GEM in IC resulted in an increase of 0.14 ngm3 in the monthly average of total mercury concentration, and 250 ngm2 in the monthly total deposition. Varying reactive gaseous mercury (RGM) or particulate mercury (PHg) in BC/IC has much less significant impact. Simulation results at different grid resolutions show good agreement (slope 0.950 1.026, r 0.816 0.973) in mercury concentration, dry deposition, and total deposition. The agreement in wet deposition is somewhat weaker (slope 0.770 0.794, r 0.685 0.892) due to the difference in emission dilution and simulated precipitation that subsequently change reaction rates in the aqueous phase. Replacing the aqueous Hg(II)-HO2 reduction by either RGM reduction by CO (51018cm3 molecule1 s1) or photoreduction of RGM (1105 s1) gives significantly better model agreement with the wet deposition measured by Mercury Deposition Network (MDN). Possible ranges of the reduction rates are estimated based on model sensitivity results. The kinetic estimate requires further verification by laboratory studies.

Lin, Che-Jen [ORNL; Pongprueksa, Pruek [Lamar University; Lindberg, Steven Eric [ORNL; Jang, Carey [U.S. Environmental Protection Agency, Raleigh, North Carolina; Braverman, Thomas [U.S. Environmental Protection Agency, Raleigh, North Carolina; Bullock, Russell O [NOAA; Ho, Thomas [ORNL; Chu, Hsing-Wei [Lamar University

2008-03-01T23:59:59.000Z

28

Application of atomic vapor laser isotope separation to the enrichment of mercury  

SciTech Connect (OSTI)

Workers at GTE/Sylvania have shown that the efficiency of fluorescent lighting may be markedly improved using mercury that has been enriched in the /sup 196/Hg isotope. A 5% improvement in the efficiency of fluorescent lighting in the United States could provide a savings of $450 million dollars in the corresponding reduction of electrical power consumption. We discuss the results of recent work done at our laboratory to develop a process for enriching mercury. The discussion centers around the results of spectroscopic measurements of excited-state lifetimes, photoionization cross sections, and isotope shifts.

Crane, J.; Erbert, G.; Paisner, J.; Chen, H.; Chiba, Z.; Beeler, R.; Combs, R.; Mostek, S.

1986-09-01T23:59:59.000Z

29

Determination of Mercury in Coal by Isotope Dilution Cold-Vapor Generation Inductively  

E-Print Network [OSTI]

Articles Determination of Mercury in Coal by Isotope Dilution Cold-Vapor Generation Inductively. Approximately 93% of U.S. coal consumption is used to generate electricity, and the U.S. EPA has estimated2 developed for high-accuracy determinations of mer- cury in bituminous and sub-bituminous coals. A closed

30

Vapor-liquid equilibria of coal-derived liquids; 3: Binary systems with tetralin at 200 mmHg  

SciTech Connect (OSTI)

Isobaric vapor-liquid equilibrium data are reported for binary systems of tetralin with p-xylene, [gamma]-picoline, piperidine, and pyridine; all systems were measured at 26.66 kPa (200 mmHg) with a recirculation still. Liquid-phase activity coefficients were correlated using the Van Laar, Wilson, NRTL, and UNIQUAC equations. Vapor-phase nonidealities were found negligible under the experimental conditions of this work, and deviations of the liquid phase from the ideal behavior, as described by Raoult's law, were found to be slightly positive for all the systems.

Blanco, B.; Beltran, S.; Cabezas, J.L. (University Coll., Burgos (Spain). Dept. of Chemical Engineering); Coca, J. (Univ. of Oviedo (Spain). Dept. of Chemical Engineering)

1994-01-01T23:59:59.000Z

31

Mercury Calibration System  

SciTech Connect (OSTI)

U.S. Environmental Protection Agency (EPA) Performance Specification 12 in the Clean Air Mercury Rule (CAMR) states that a mercury CEM must be calibrated with National Institute for Standards and Technology (NIST)-traceable standards. In early 2009, a NIST traceable standard for elemental mercury CEM calibration still does not exist. Despite the vacature of CAMR by a Federal appeals court in early 2008, a NIST traceable standard is still needed for whatever regulation is implemented in the future. Thermo Fisher is a major vendor providing complete integrated mercury continuous emissions monitoring (CEM) systems to the industry. WRI is participating with EPA, EPRI, NIST, and Thermo Fisher towards the development of the criteria that will be used in the traceability protocols to be issued by EPA. An initial draft of an elemental mercury calibration traceability protocol was distributed for comment to the participating research groups and vendors on a limited basis in early May 2007. In August 2007, EPA issued an interim traceability protocol for elemental mercury calibrators. Various working drafts of the new interim traceability protocols were distributed in late 2008 and early 2009 to participants in the Mercury Standards Working Committee project. The protocols include sections on qualification and certification. The qualification section describes in general terms tests that must be conducted by the calibrator vendors to demonstrate that their calibration equipment meets the minimum requirements to be established by EPA for use in CAMR monitoring. Variables to be examined include linearity, ambient temperature, back pressure, ambient pressure, line voltage, and effects of shipping. None of the procedures were described in detail in the draft interim documents; however they describe what EPA would like to eventually develop. WRI is providing the data and results to EPA for use in developing revised experimental procedures and realistic acceptance criteria based on actual capabilities of the current calibration technology. As part of the current effort, WRI worked with Thermo Fisher elemental mercury calibrator units to conduct qualification experiments to demonstrate their performance characteristics under a variety of conditions and to demonstrate that they qualify for use in the CEM calibration program. Monitoring of speciated mercury is another concern of this research. The mercury emissions from coal-fired power plants are comprised of both elemental and oxidized mercury. Current CEM analyzers are designed to measure elemental mercury only. Oxidized mercury must first be converted to elemental mercury prior to entering the analyzer inlet in order to be measured. CEM systems must demonstrate the ability to measure both elemental and oxidized mercury. This requires the use of oxidized mercury generators with an efficient conversion of the oxidized mercury to elemental mercury. There are currently two basic types of mercuric chloride (HgCl{sub 2}) generators used for this purpose. One is an evaporative HgCl{sub 2} generator, which produces gas standards of known concentration by vaporization of aqueous HgCl{sub 2} solutions and quantitative mixing with a diluent carrier gas. The other is a device that converts the output from an elemental Hg generator to HgCl{sub 2} by means of a chemical reaction with chlorine gas. The Thermo Fisher oxidizer system involves reaction of elemental mercury vapor with chlorine gas at an elevated temperature. The draft interim protocol for oxidized mercury units involving reaction with chlorine gas requires the vendors to demonstrate high efficiency of oxidation of an elemental mercury stream from an elemental mercury vapor generator. The Thermo Fisher oxidizer unit is designed to operate at the power plant stack at the probe outlet. Following oxidation of elemental mercury from reaction with chlorine gas, a high temperature module reduces the mercuric chloride back to elemental mercury. WRI conducted work with a custom laboratory configured stand-alone oxidized mercury generator unit prov

John Schabron; Eric Kalberer; Joseph Rovani; Mark Sanderson; Ryan Boysen; William Schuster

2009-03-11T23:59:59.000Z

32

Understanding mercury demethylation is the key to decrease the high environmental levels of the neurotoxin methyl-Hg in lakes.  

E-Print Network [OSTI]

dynamics of MeHg is the net result of three major processes: 1) formation by Hg methylation 2) degradation (demethylation) and Hg2+ reduction to Hg0 and evasion to the atmosphere. The major process of MeHg degradation is driven by UV light in surface waters. Although biotic demethylation processes are less well understood

Uppsala Universitet

33

Performance of copper chloride-impregnated sorbents on mercury vapor control in an entrained-flow reactor system  

SciTech Connect (OSTI)

An entrained-flow system has been designed and constructed to simulate in-flight mercury (Hg) capture by sorbent injection in ducts of coal-fired utility plants. The test conditions of 1.2-sec residence time, 140{degree}C gas temperature, 6.7 m/sec (22 ft/sec) gas velocity, and 0-0.24 g/m{sup 3} (0-15 lbs of sorbent per 1 million actual cubic feet of flue gas sorbent injection rates were chosen to simulate conditions in the ducts. Four kinds of sorbents were used in this study. Darco Hg-LH (lignite-based) served as a benchmark sorbent with which Hg control capability of other sorbents could be compared. Also, Darco-FGD (lignite-based) was used as a representative raw activated carbon sorbent. Two different copper chloride-impregnated sorbents were developed in the laboratory and tested in the entrained-flow system to examine the possibility of using these sorbents at coal-fired power plants. The test results showed that one of the copper chloride sorbents has remarkable elemental mercury (Hg{sup 0}) oxidation capability, and the other sorbent demonstrated a better performance in Hg removal than Darco Hg-LH. 13 refs., 4 figs., 3 tabs.

Sang-Sup Lee; Joo-Youp Lee; Tim C. Keener [University of Cincinnati, Cincinnati, OH (United States). Department of Civil and Environmental Engineering

2008-11-15T23:59:59.000Z

34

10.1177/0270467603259787ARTICLEBULLETIN OF SCIENCE, TECHNOLOGY & SOCIETY / October 2003Roe / FISHING FOR IDENTITY Fishing for Identity: Mercury Contamination  

E-Print Network [OSTI]

of mercury in the United States. During 1999, total mercury emis- sions from power plant emissions exceeded (HG0 ), inorganic mercury (HG2+ ), and methyl mercury (MeHg), methyl mercury poses the greatest threat

Delaware, University of

35

In situ mercury stabilization  

SciTech Connect (OSTI)

BNL Royalty Project Internal Status Report. The funds from the allotment of royalty income were used to experimentally explore feasibility of related, potential new techniques based on the Environmental Sciences Department successful technology licensed for the ex situ treatment of mercury. Specifically, this work is exploring the concept of using Sulfur Polymer Cement (SPC) in an in situ application to stabilize and/or remove mercury (Hg) from surficial soil. Patent disclosure forms have been filed for this process. Soil was artificially spiked with 500 ppm Hg and a series of experiments were set up in which SPC rods were placed in the center of a mass of this soil. Some experiments were conducted at 20 C and others at 50 C. After times ranging from 11 to 24 days, these experiments were opened, photographed and the soil was sampled from discrete locations in the containers. The soil and SPC samples were analyzed for Fe and Hg by x-ray fluorescence. The Hg profile in the soil was significantly altered, with concentrations along the outer edge of the soil reduced by as much as 80% from the starting concentration. Conversely, closer to the treatment rod containing SPC, concentrations of Hg were significantly increased over the original concentration. Preliminary results for elevated temperature sample are shown graphically in Figure 2. Apparently the Hg had migrated toward the SPC and reacted with sulfur to form Hg S. This appears to be a reaction between gaseous phases of both S and Hg, with Hg having a greater vapor pressure. The concentration of low solubility HgS (i.e., low leaching properties) developed within 11 days at 50 C and 21 days at 20 C, confirming the potential of this concept.

Fuhrmann, M.; Kalb, P.; Adams, J.

2004-09-01T23:59:59.000Z

36

Hg Anomalies In Soils- A Geochemical Exploration Method For Geothermal...  

Open Energy Info (EERE)

Areas. Geothermics. () . Related Geothermal Exploration Activities Activities (5) Mercury Vapor At Breitenbush Hot Springs Area (Varekamp & Buseck, 1983) Mercury Vapor At...

37

Final Report - Molecular Mechanisms of Bacterial Mercury Transformation - UCSF  

SciTech Connect (OSTI)

The bacterial mercury resistance (mer) operon functions in Hg biogeochemistry and bioremediation by converting reactive inorganic Hg(II) and organic [RHg(II)]1+ mercurials to relatively inert monoatomic mercury vapor, Hg(0). Its genes regulate operon expression (MerR, MerD, MerOP), import Hg(II) (MerT, MerP, and MerC), and demethylate (MerB) and reduce (MerA) mercurials. We focus on how these components interact with each other and with the host cell to allow cells to survive and detoxify Hg compounds. Understanding how this ubiquitous detoxification system fits into the biology and ecology of its bacterial host is essential to guide interventions that support and enhance Hg remediation. In the current overall project we focused on two aspects of this system: (1) investigations of the energetics of Hg(II)-ligand binding interactions, and (2) both experimental and computational approaches to investigating the molecular mechanisms of Hg(II) acquisition by MerA and intramolecular transfer of Hg(II) prior to reduction within the MerA enzyme active site. Computational work was led by Prof. Jeremy Smith and took place at the University of Tennessee, while experimental work on MerA was led by Prof. Susan Miller and took place at the University of California San Francisco.

Miller, Susan M. [UCSF

2014-04-24T23:59:59.000Z

38

Mercury Detection with Gold Nanoparticles  

E-Print Network [OSTI]

R. J. Warmack, Detection of mercury vapor using resonatingA surface acoustic wave mercury vapor sensor, Ieee Trans.N. E. Selin, Integrating mercury science and policy in the

Crosby, Jeffrey

2013-01-01T23:59:59.000Z

39

MERCURY OXIDIZATION IN NON-THERMAL PLASMA BARRIER DISCHARGE SYSTEM  

SciTech Connect (OSTI)

In the past decade, the emission of toxic elements from human activities has become a matter of great public concern. Hg, As, Se and Cd typically volatilize during a combustion process and are not easily caught with conventional air pollution control techniques. In addition, there is no pollution prevention technique available now or likely be available in the foreseeable future that can prevent the emission of these trace elements. These trace elements pose additional scientific challenge as they are present at only ppb levels in large gas streams. Mercury, in particular, has attracted significant attention due to its high volatility, toxicity and potential threat to human health. In the present research work, a non-thermal plasma dielectric barrier discharge technique has been used to oxidize Hg{sup 0}(g) to HgO. The basic premise of this approach is that Hg{sup 0} in vapor form cannot be easily removed in an absorption tower whereas HgO as a particulate is amiable to water scrubbing. The work presented in this report consists of three steps: (1) setting-up of an experimental apparatus to generate mercury vapors at a constant rate and modifying the existing non-thermal plasma reactor system, (2) solving the analytical challenge for measuring mercury vapor concentration at ppb level, and (3) conducting experiments on mercury oxidation under plasma conditions to establish proof of concept.

V.K. Mathur

2003-02-01T23:59:59.000Z

40

Hg System Assembly and Testing Status  

E-Print Network [OSTI]

#12;2VRVS Meeting 8 Nov 2006 OAK RIDGE NATIONAL LABORATORY U. S. DEPARTMENT OF ENERGY Hg Drain & Spill Ports Completed Hg drain from cylinder Hg leak sump with float switch Hg spill extraction port #12;3VRVS Meeting 8 Nov 2006 OAK RIDGE NATIONAL LABORATORY U. S. DEPARTMENT OF ENERGY Local Hg Vapor Filters · Hg

McDonald, Kirk

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


41

Exploiting the Higher Specificity of Silver Amalgamation: Selective Detection of Mercury(II) by Forming Ag/Hg Amalgam  

E-Print Network [OSTI]

, 32611-7200, United States *S Supporting Information ABSTRACT: Heavy metal ion pollution poses severe and biological samples. Contamination of the environment with heavy metal ions has been an important concern selective for Hg2+ and does not respond to other metal ions with up to millimolar concentration levels

Tan, Weihong

42

Recovery of mercury from mercury compounds via electrolytic methods  

DOE Patents [OSTI]

A process for electrolytically recovering mercury from mercury compounds is provided. In one embodiment, Hg is recovered from Hg.sub.2 Cl.sub.2 employing as the electrolyte solution a mixture of HCl and H.sub.2 O. In another embodiment, Hg is electrolytically recovered from HgO wherein the electrolyte solution is comprised of glacial acetic acid and H.sub.2 O. Also provided is an apparatus for producing isotopically enriched mercury compounds in a reactor and then transporting the dissolved compounds into an electrolytic cell where mercury ions are electrolytically reduced and elemental mercury recovered from the mercury compounds.

Grossman, Mark W. (Belmont, MA); George, William A. (Rockport, MA)

1989-01-01T23:59:59.000Z

43

Recovery of mercury from mercury compounds via electrolytic methods  

DOE Patents [OSTI]

A process for electrolytically recovering mercury from mercury compounds is provided. In one embodiment, Hg is recovered from Hg[sub 2]Cl[sub 2] employing as the electrolyte solution a mixture of HCl and H[sub 2]O. In another embodiment, Hg is electrolytically recovered from HgO wherein the electrolyte solution is comprised of glacial acetic acid and H[sub 2]O. Also provided is an apparatus for producing isotopically enriched mercury compounds in a reactor and then transporting the dissolved compounds into an electrolytic cell where mercury ions are electrolytically reduced and elemental mercury recovered from the mercury compounds. 3 figures.

Grossman, M.W.; George, W.A.

1991-06-18T23:59:59.000Z

44

Recovery of mercury from mercury compounds via electrolytic methods  

DOE Patents [OSTI]

A process for electrolytically recovering mercury from mercury compounds is provided. In one embodiment, Hg is recovered from Hg.sub.2 Cl.sub.2 employing as the electrolyte solution a mixture of HCl and H.sub.2 O. In another embodiment, Hg is electrolytically recovered from HgO wherein the electrolyte solution is comprised of glacial acetic acid and H.sub.2 O. Also provided is an apparatus for producing isotopically enriched mercury compounds in a reactor and then transporting the dissolved compounds into an electrolytic cell where mercury ions are electrolytically reduced and elemental mercury recovered from the mercury compounds.

Grossman, Mark W. (Belmont, MA); George, William A. (Rockport, MA)

1988-01-01T23:59:59.000Z

45

Recovery of mercury from mercury compounds via electrolytic methods  

DOE Patents [OSTI]

A process for electrolytically recovering mercury from mercury compounds is provided. In one embodiment, Hg is recovered from Hg.sub.2 Cl.sub.2 employing as the electrolyte solution a mixture of HCl and H.sub.2 O. In another embodiment, Hg is electrolytically recovered from HgO wherein the electrolyte solution is comprised of glacial acetic acid and H.sub.2 O. Also provided is an apparatus for producing isotopically enriched mercury compounds in a reactor and then transporting the dissolved compounds into an electrolytic cell where mercury ions are electrolytically reduced and elemental mercury recovered from the mercury compounds.

Grossman, Mark W. (Belmont, MA); George, William A. (Rockport, MA)

1991-01-01T23:59:59.000Z

46

Recovery of mercury from mercury compounds via electrolytic methods  

DOE Patents [OSTI]

A process for electrolytically recovering mercury from mercury compounds is provided. In one embodiment, Hg is recovered from Hg[sub 2]Cl[sub 2] employing as the electrolyte solution a mixture of HCl and H[sub 2]O. In another embodiment, Hg is electrolytically recovered from HgO wherein the electrolyte solution is comprised of glacial acetic acid and H[sub 2]O. Also provided is an apparatus for producing isotopically enriched mercury compounds in a reactor and then transporting the dissolved compounds into an electrolytic cell where mercury ions are electrolytically reduced and elemental mercury recovered from the mercury compounds. 3 figs.

Grossman, M.W.; George, W.A.

1989-11-07T23:59:59.000Z

47

Constraining Mercury Oxidation Using Wet Deposition  

E-Print Network [OSTI]

Constraining Mercury Oxidation Using Wet Deposition Noelle E. Selin and Christopher D. Holmes mercury oxidation [Selin & Jacob, Atmos. Env. 2008] 30 60 90 120 150 30 60 90 120 150 30 60 90 120 150 30 Influences on Mercury Wet Deposition · Hg wet dep = f(precipitation, [Hg(II)+Hg(P)]) Correlation (r2) between

Selin, Noelle Eckley

48

NOVEL PROCESS FOR REMOVAL AND RECOVERY OF VAPOR-PHASE MERCURY  

SciTech Connect (OSTI)

The goal of this project is to investigate the use of a regenerable sorbent for removing and recovering mercury from the flue gas of coal-fired power plants. The process is based on the sorption of mercury by noble metals and the thermal regeneration of the sorbent, recovering the desorbed mercury in a small volume for recycling or disposal. The project was carried out in two phases, covering five years. Phase I ran from September 1995 through September 1997 and involved development and testing of sorbent materials and field tests at a pilot coal-combustor. Phase II began in January 1998 and ended September 2000. Phase II culminated with pilot-scale testing at a coal-fired power plant. The use of regenerable sorbents holds the promise of capturing mercury in a small volume, suitable for either stable disposal or recycling. Unlike single-use injected sorbents such as activated carbon, there is no impact on the quality of the fly ash. During Phase II, tests were run with a 20-acfm pilot unit on coal-combustion flue gas at a 100 lb/hr pilot combustor and a utility boiler for four months and six months respectively. These studies, and subsequent laboratory comparisons, indicated that the sorbent capacity and life were detrimentally affected by the flue gas constituents. Sorbent capacity dropped by a factor of 20 to 35 during operations in flue gas versus air. Thus, a sorbent designed to last 24 hours between recycling lasted less than one hour. The effect resulted from an interaction between SO{sub 2} and either NO{sub 2} or HCl. When SO{sub 2} was combined with either of these two gases, total breakthrough was seen within one hour in flue gas. This behavior is similar to that reported by others with carbon adsorbents (Miller et al., 1998).

Craig S. Turchi

2000-09-29T23:59:59.000Z

49

Methods for dispensing mercury into devices  

DOE Patents [OSTI]

A process for dispensing mercury into devices which requires mercury. Mercury is first electrolytically separated from either HgO or Hg.sub.2 Cl.sub.2 and plated onto a cathode wire. The cathode wire is then placed into a device requiring mercury.

Grossman, Mark W. (Belmont, MA); George, William A. (Rockport, MA)

1987-04-28T23:59:59.000Z

50

Methods for dispensing mercury into devices  

DOE Patents [OSTI]

A process is described for dispensing mercury into devices which requires mercury. Mercury is first electrolytically separated from either HgO or Hg[sub 2]Cl[sub 2] and plated onto a cathode wire. The cathode wire is then placed into a device requiring mercury. 2 figs.

Grossman, M.W.; George, W.A.

1987-04-28T23:59:59.000Z

51

Direct vapor/solid synthesis of mercuric iodide using compounds of mercury and iodine  

SciTech Connect (OSTI)

A process is disclosed for producing high purity mercuric iodide by passing a gaseous source of a mercuric compound through a particulate bed of a low vapor pressure iodide compound which is maintained at an elevated temperature which is the lower of either: (a) just below the melting or volatilization temperature of the iodide compound (which ever is lower); or (b) just below the volatilization point of the other reaction product formed during the reaction; to cause the mercuric compound to react with the iodide compound to form mercuric iodide which then passes as a vapor out of the bed into a cooler condensation region.

Skinner, Nathan L. (Carpinteria, CA)

1990-01-01T23:59:59.000Z

52

Mercury Strategic Plan Outfall 200 Mercury Treatment Facility  

Office of Environmental Management (EM)

Partial LMR * Alpha-5 LMR & Bldg Characterization * S&M mercury removal * Hg waterfishsediment studies * Technology Development Plan * Debris treatability study * Fate and...

53

Removal of elemental mercury (Hg(0)) by nanosized V{sub 2}O{sub 5}/TiO{sub 2} catalysts  

SciTech Connect (OSTI)

Novel reactive nanosized V{sub 2}O{sub 5}/TiO{sub 2} catalysts (aerogel, xerogel, and impregnated catalysts) for the removal of Hg{sup 0} and their synthesis methods have been introduced in this research. Aerogel catalyst has the highest surface area among the catalysts synthesized in this research and contained reactive monovanadates on its surfaces resulting in higher reactivity for the Hg{sup 0} removal than impregnated and selective catalytic reduction catalysts. XPS analyses on the surfaces of nanosized catalysts after the removal of Hg{sup 0} suggest that adsorbed Hg{sup 0} oxidatively transformed to Hg{sup O} by surface vanadates (mono- and poly vanadates), consistent with the Mars-Maessen mechanism. Early column breakthrough has been observed at temperatures above 300{sup o}C due mainly to the desorption of Hg{sup 0} from the catalyst surfaces. The decrease in Hg{sup 0} concentration and increase in catalyst content in a column reactor have increased the removal of Hg{sup 0}, indicating that the removal is a heterogeneous surface-limited reaction. At 400{sup o}C, the catalysts under air flow have shown a higher Hg{sup 0} removal because gas-phase oxygen from the flow could provide an oxygen-rich environment for producing more oxidized vanadate species on their surfaces. No significant difference in the Hg{sup 0} removal between different gas types (nitrogen and air) has been observed at 100{sup o}C. 27 refs., 5 figs.

Lee, W.; Bae, G.N. [Korea Advanced Institute of Science and Technology, Daejeon (Republic of Korea)

2009-03-01T23:59:59.000Z

54

Atmospheric Mercury Deposition during the Last 270 Years: A  

E-Print Network [OSTI]

Atmospheric Mercury Deposition during the Last 270 Years: A Glacial Ice Core Record of Natural, and U.S. Geological Survey, Wisconsin District Mercury Research Laboratory, Middleton, Wisconsin 53562 Mercury (Hg) contamination of aquatic ecosystems and subsequent methylmercury bioaccumulation

55

Wavelengths, Energy Level Classifications, and Energy Levels for the Spectrum of Neutral Mercury  

E-Print Network [OSTI]

Wavelengths, Energy Level Classifications, and Energy Levels for the Spectrum of Neutral Mercury E of neutral mercury Hg I for both the single isotope 198 Hg and for mercury in its natural isotopic abundance of neutral mercury for both 198 Hg and the natural isotopic mixture. Tabular data for 105 classified lines

Magee, Joseph W.

56

Mercury and Other Heavy Metals Influence Bacterial Community Structure in Contaminated Streams  

E-Print Network [OSTI]

Mercury and Other Heavy Metals Influence Bacterial Community Structure in Contaminated Streams Research The influences of uranium (U), mercury (Hg) and methylmercury (MeHg) on the microbial community. #12;High concentrations of uranium, inorganic mercury, Hg(II) and methymercury (MeHg) have been

57

Investigation of modified speciation for enhanced control of mercury  

SciTech Connect (OSTI)

Mercury was identified as a hazardous air pollutant in Title 3 of the 1990 Clean Air Act Amendments. It has been singled out for particular scrutiny because of its behavior in the environment (bioaccumulation) and its potential for deleterious effects on humans and wildlife. After studying the sources of mercury in the environment, the US Environmental Protection Agency has concluded that coal-fired boilers generate a significant fraction of the total anthropogenic emissions. Therefore, the agency is currently considering whether to impose mercury control requirements on coal-fired boilers in the electric utility industry. However, the costs for potential control measures (such as sorbent injection) can be extremely high. Mercury removal with chloric acid solutions was tested. The presence of NO increased Hg removal. It appeared that both gas-gas and gas-liquids reactions were operating, with the gas-phase reactions involving NO becoming increasingly important as the solute concentration was raised. From these studies, it was concluded that even higher Hg{sup 0} removals could be obtained if more of the reagent was made available for reaction in the gas phase. For this reason (and also to simulate a more real-world duct-injection process) a new series of tests was initiated in which an ultrasonic atomizer was used to inject small droplets of the oxidizing solutions into a flowing gas stream containing Hg{sup 0} vapors and other typical flue-gas components. The results of those tests are described in this paper.

Livengood, C.D.; Mendelsohn, M.H.

1998-08-01T23:59:59.000Z

58

Mercury Detection with Gold Nanoparticles  

E-Print Network [OSTI]

samples by cold vapor-atomic absorption spectrometry, J.S. Gucer, Direct atomic absorption determination of mercuryL. A. Vasilieva, Direct atomic absorption determination of

Crosby, Jeffrey

2013-01-01T23:59:59.000Z

59

Homogeneous and Heterogeneous Reaction and Transformation of Hg and Trace Metals in Combustion Systems  

SciTech Connect (OSTI)

The overall goal of this project was to produce a working dynamic model to predict the transformation and partitioning of trace metals resulting from combustion of a broad range of fuels. The information provided from this model will be instrumental in efforts to identify fuels and conditions that can be varied to reduce metal emissions. Through the course of this project, it was determined that mercury (Hg) and arsenic (As) would be the focus of the experimental investigation. Experiments were therefore conducted to examine homogeneous and heterogeneous mercury oxidation pathways, and to assess potential interactions between arsenic and calcium. As described in this report, results indicated that the role of SO{sub 2} on Hg oxidation was complex and depended upon overall gas phase chemistry, that iron oxide (hematite) particles contributed directly to heterogeneous Hg oxidation, and that As-Ca interactions occurred through both gas-solid and within-char reaction pathways. Modeling based on this study indicated that, depending upon coal type and fly ash particle size, vaporization-condensation, vaporization-surface reaction, and As-CaO in-char reaction all play a role in arsenic transformations under combustion conditions.

J. Helble; Clara Smith; David Miller

2009-08-31T23:59:59.000Z

60

The Homogeneus Forcing of Mercury Oxidation to provide Low-Cost Capture  

SciTech Connect (OSTI)

Trace amounts of mercury are found in all coals. During combustion, or during thermal treatment in advanced coal processes, this mercury is vaporized and can be released to the atmosphere with the ultimate combustion products. This has been a cause for concern for a number of years, and has resulted in a determination by the EPA to regulate and control these emissions. Present technology does not, however, provide inexpensive ways to capture or remove mercury. Mercury that exits the furnace in the oxidized form (HgCl{sub 2}) is known to much more easily captured in existing pollution control equipment (e.g., wet scrubbers for SO{sub 2}), principally due to its high solubility in water. Work funded by DOE has helped understand the chemical kinetic processes that lead to mercury oxidation in furnaces. The scenario is as follows. In the flame the mercury is quantitatively vaporized as elemental mercury. Also, the chlorine in the fuel is released as HCl. The direct reaction Hg+HCl is, however, far too slow to be of practical consequence in oxidation. The high temperature region does supports a small concentration of atomic chlorine. As the gases cool (either in the furnace convective passes, in the quench prior to cold gas cleanup, or within a sample probe), the decay in Cl atom is constrained by the slowness of the principal recombination reaction, Cl+Cl+M{yields}Cl{sub 2}+M. This allows chlorine atom to hold a temporary, local superequilibrium concentration . Once the gases drop below about 550 C, the mercury equilibrium shifts to favor HgCl{sub 2} over Hg, and this superequilibrium chlorine atom promotes oxidation via the fast reactions Hg+Cl+M{yields}HgCl+M, HgCl+Cl+M{yields}HgCl{sub 2}+M, and HgCl+Cl{sub 2}{yields}HgCl{sub 2}+Cl. Thus, the high temperature region provides the Cl needed for the reaction, while the quench region allows the Cl to persist and oxidize the mercury in the absence of decomposition reactions that would destroy the HgCl{sub 2}. Promoting mercury oxidation is one means of getting moderate-efficiency, 'free' mercury capture when wet gas cleanup systems are already in place. The chemical kinetic model we developed to describe the oxidation process suggests that in fuel lean gases, the introduction of trace amounts of H{sub 2} within the quench region leads to higher Cl concentrations via chain branching. The amount of additive, and the temperature at the addition point are critical. We investigated this process in a high-temperature quartz flow reactor. The results do indicate a substantial amount of promotion of oxidation with the introduction of relatively small amounts of hydrogen at around 1000 K ({approx}100 ppm relative to the furnace gas). In practical systems the source of this hydrogen is likely to be a small natural gas steam reformer. This would also produce CO, so co-injection of CO was also tested. The CO did not provide any additional promotion, and in some cases led to a reduction in oxidation. We also examined the influence of NO and SO{sub 2} on the promotion process. We did not see any influence under the conditions examined. The present results were for a 0.5 s, isothermal plug flow environment. The next step should be to determine the appropriate injection point for the hydrogen and the performance under realistic temperature quench conditions. This could be accomplished first by chemical kinetic modeling, and then by tunnel flow experiment.

John Kramlich; Linda Castiglone

2007-06-30T23:59:59.000Z

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


61

Apparatus for mercury refinement  

DOE Patents [OSTI]

The effluent from mercury collected during the photochemical separation of the [sup 196]Hg isotope is often contaminated with particulate mercurous chloride, Hg[sub 2]Cl[sub 2]. The use of mechanical filtering via thin glass tubes, ultrasonic rinsing with acetone (dimethyl ketone) and a specially designed cold trap have been found effective in removing the particulate (i.e., solid) Hg[sub 2]Cl[sub 2] contaminant. The present invention is particularly directed to such filtering. 5 figures.

Grossman, M.W.; Speer, R.; George, W.A.

1991-07-16T23:59:59.000Z

62

Method for mercury refinement  

DOE Patents [OSTI]

The effluent from mercury collected during the photochemical separation of the [sup 196]Hg isotope is often contaminated with particulate mercurous chloride, Hg[sub 2]Cl[sub 2]. The use of mechanical filtering via thin glass tubes, ultrasonic rinsing with acetone (dimethyl ketone) and a specially designed cold trap have been found effective in removing the particulate (i.e., solid) Hg[sub 2]Cl[sub 2] contaminant. The present invention is particularly directed to such filtering. 5 figures.

Grossman, M.W.; Speer, R.; George, W.A.

1991-04-09T23:59:59.000Z

63

Method for mercury refinement  

DOE Patents [OSTI]

The effluent from mercury collected during the photochemical separation of the .sup.196 Hg isotope is often contaminated with particulate mercurous chloride, Hg.sub.2 Cl.sub.2. The use of mechanical filtering via thin glass tubes, ultrasonic rinsing with acetone (dimethyl ketone) and a specially designed cold trap have been found effective in removing the particulate (i.e., solid) Hg.sub.2 Cl.sub.2 contaminant. The present invention is particularly directed to such filtering.

Grossman, Mark W. (Belmont, MA); Speer, Richard (Reading, MA); George, William A. (Rockport, MA)

1991-01-01T23:59:59.000Z

64

Apparatus for mercury refinement  

DOE Patents [OSTI]

The effluent from mercury collected during the photochemical separation of the .sup.196 Hg isotope is often contaminated with particulate mercurous chloride, Hg.sub.2 Cl.sub.2. The use of mechanical filtering via thin glass tubes, ultrasonic rinsing with acetone (dimethyl ketone) and a specially designed cold trap have been found effective in removing the particulate (i.e., solid) Hg.sub.2 Cl.sub.2 contaminant. The present invention is particularly directed to such filtering.

Grossman, Mark W. (Belmont, MA); Speer, Richard (Reading, MA); George, William A. (Rockport, MA)

1991-01-01T23:59:59.000Z

65

Method for the removal and recovery of mercury  

DOE Patents [OSTI]

The present invention is an enhanced method for the removal and recovery of mercury from mercury-contaminated matrices. The method involves contacting a mercury-contaminated matrix with an aqueous dispersant solution derived from specific intra-amoebic isolates to release the mercury from the mercury-contaminated matrix and emulsify the mercury; then, contacting the matrix with an amalgamating metal from a metal source to amalgamate the mercury to the amalgamating metal; removing the metallic source from the mercury-contaminated matrix; and heating the metallic source to vaporize the mercury in a closed system to capture the mercury vapors.

Easterly, C.E.; Vass, A.A.; Tyndall, R.L.

1997-01-28T23:59:59.000Z

66

Method for the removal and recovery of mercury  

DOE Patents [OSTI]

The present invention is an enhanced method for the removal and recovery of mercury from mercury-contaminated matrices. The method involves contacting a mercury-contaminated matrix with an aqueous dispersant solution derived from specific intra-amoebic isolates to release the mercury from the mercury-contaminated matrix and emulsify the mercury; then, contacting the matrix with an amalgamating metal from a metal source to amalgamate the mercury to the amalgamating metal; removing the metallic source from the mercury-contaminated matrix; and heating the metallic source to vaporize the mercury in a closed system to capture the mercury vapors.

Easterly, Clay E. (Knoxville, TN); Vass, Arpad A. (Oak Ridge, TN); Tyndall, Richard L. (Clinton, TN)

1997-01-01T23:59:59.000Z

67

On-line method of determining utilization factor in Hg-196 photochemical separation process  

DOE Patents [OSTI]

The present invention is directed to a method for determining the utilization factor [U] in a photochemical mercury enrichment process (.sup.196 Hg) by measuring relative .sup.196 Hg densities using absorption spectroscopy.

Grossman, Mark W. (Belmont, MA); Moskowitz, Philip E. (Peabody, MA)

1992-01-01T23:59:59.000Z

68

Mercury Methylation in Mine Wastes Collected from Abandoned Mercury Mines in the USA  

SciTech Connect (OSTI)

Mercury mines contain highly elevated Hg contents, but more problematic environmentally are elemental Hg and soluble Hg salts produced during ore retorting that remain in wastes at mine sites. Under certain conditions, these inorganic Hg compounds convert to bioavailable, highly toxic organic Hg forms. Speciation and transformation of Hg was studied in wastes collected from abandoned Hg mines at McDermitt, NV, and Terlingua, TX, which are moderate size on an international scale and produced about 10,000 and 5,000 t of elemental Hg, respectively. In waste samples, we measured total Hg and methyl-Hg contents, identified various Hg compounds using Hg-thermo-desorption pyrolysis, and determined rates of Hg methylation and methyl-Hg demethylation using isotopic-tracer methods. Pyrolysis analysis of mine wastes showed variable amounts of cinnabar, metacinnabar, Hg salts, elemental Hg, and elemental Hg sorbed onto particulates such as clay and Fe-oxides. Mine wastes with the highest methyl-Hg contents correspond to those with elemental Hg and particulate-sorbed elemental Hg, and also produced the highest laboratory-estimated potential Hg methylation rates, as much as 4.8%/day. Samples containing dominantly cinnabar showed little or no Hg methylation. Mine wastes with high methyl-Hg contents generally showed low methyl-Hg demethylation, suggesting that Hg methylation was dominant. Both mines are located in semiarid climates, and during this study, streambeds below the mines were dry. Total Hg contents in stream sediment collected below the mines show significant dilution, and methyl-Hg contents were typically below the limit of determination. Methylation of Hg downstream from Hg mines is probably lower in arid climates due to lack of mine-water runoff and lower microbial activity. The correspondence of mine wastes containing elemental Hg and high methyl-Hg contents suggests that Hg0 oxidizes to Hg2+, which is subsequently bioavailable for microbial Hg methylation.

Gray, John E. (U.S. Geological Survey); Hines, Mark E. (Massachusetts, Univ Of); Biester, Harald (Heidelberg College); Lasorsa, Brenda K. (BATTELLE (PACIFIC NW LAB))

2003-05-01T23:59:59.000Z

69

Mercury Spill Information and Response Guidance  

E-Print Network [OSTI]

Mercury Spill Information and Response Guidance Background Information Mercury can be found, plumbing traps and vacuum pumps. When mercury is spilled, it forms beads or droplets that can accumulate mercury vapors can be very dangerous, depending on the amount inhaled and the length of exposure

Holland, Jeffrey

70

COMBINED THEORETICAL AND EXPERIMENTAL INVESTIGATION OF MECHANISMS AND KINETICS OF VAPOR-PHASE MERCURY UPTAKE BY CARBONACOUES SURFACES  

SciTech Connect (OSTI)

The first part of this study evaluated the application of a versatile optical technique to study the adsorption and desorption of model adsorbates representative of volatile polar (acetone) and non-polar (propane) organic compounds on a model carbonaceous surface under ultra high vacuum (UHV) conditions. The results showed the strong correlation between optical differential reflectance (ODR) and adsorbate coverage determined by temperature programmed desorption (TPD). ODR technique was proved to be a powerful tool to investigate surface adsorption and desorption from UHV to high pressure conditions. The effects of chemical functionality and surface morphology on the adsorption/desorption behavior of acetone, propane and mercury were investigated for two model carbonaceous surfaces, namely air-cleaved highly oriented pyrolytic graphite (HOPG) and plasma-oxidized HOPG. They can be removed by thermal treatment (> 500 K). The presence of these groups almost completely suppresses propane adsorption at 90K and removal of these groups leads to dramatic increase in adsorption capacity. The amount of acetone adsorbed is independent of surface heat treatment and depends only on total exposure. The effects of morphological heterogeneity is evident for plasma-oxidized HOPG as this substrate provides greater surface area, as well as higher energy binding sites. Mercury adsorption at 100 K on HOPG surfaces with and without chemical functionalities and topological heterogeneity created by plasma oxidation occurs through physisorption. The removal of chemical functionalities from HOPG surface enhances mercury physisorption. Plasma oxidation of HOPG provides additional surface area for mercury adsorption. Mercury adsorption by activated carbon at atmospheric pressure occurs through two distinct mechanisms, physisorption below 348 K and chemisorption above 348 K. No significant impact of oxygen functionalities was observed in the chemisorption region. The key findings of this study open the possibility to apply scientific information obtained from the studies with simple surfaces like HOPG under ideal conditions (UHV) to industrial sorbents under realistic process conditions. HOPG surface can be modified chemically and topologically by plasma oxidation to simulate key features of activated carbon adsorbents.

Radisav D. Vidic

2002-05-01T23:59:59.000Z

71

Dicarboxylate assisted synthesis of the monoclinic heterometallic tetrathiocyanato bridged copper(II) and mercury(II) coordination polymer {l_brace}Cu[Hg(SCN){sub 4}]{r_brace}{sub n}: Synthesis, structural, vibration, luminescence, EPR studies and DFT calculations  

SciTech Connect (OSTI)

The synthesis of the monoclinic polymorph of {l_brace}Cu[Hg(SCN){sub 4}]{r_brace}{sub n} is reported. The compound, as determined by X-ray diffraction of a twinned crystal, consists of mercury and copper atoms linked by {mu}{sub 1,3}-SCN bridges. The crystal packing shows a highly porous infinite 3D structure. Diagnostic resonances for the SCN{sup -} ligand and metal-ligand bonds in the IR, far-IR and Raman spectra are assigned and discussed. The electronic band structure along with density of states (DOS) calculated by the DFT method indicates that the compound is an indirect band gap semiconductor. The DFT calculations show that the observed luminescence of the compound arises mainly from an excited LLCT state with small MLCT contributions (from the copper to unoccupied {pi}{sup *} orbital of the thiocyanate groups). The X-band EPR spectrum of the powdered sample at room temperature reveals an axial signal with anisotropic g factors consistent with the unpaired electron of Cu(II) ion in the d{sub x}{sup 2}{sub -y}{sup 2} orbital. -- Graphical abstract: Synthesis and X-ray structure determination of the monoclinic {l_brace}Cu[Hg(SCN){sub 4}]{r_brace}{sub n} is reported. The IR, far-IR, Raman, photoluminescence as well as EPR spectra of the compound is discussed. Also, the emission and semiconducting behavior of the compound is illustrated through the density functional theory calculation of electronic band structure along with density of states. Display Omitted Research highlights: > The monoclinic {l_brace}Cu[Hg(SCN){sub 4}]{r_brace}{sub n} has been prepared. > The structure of the compound is determined by XRD of a twinned crystal. > The IR, far-IR, Raman, EPR and emission spectra of the compound is investigated. > As shown by DFT calculations, the emission bands of the compound are mainly LLCT. > Small MLCT from the copper to the thiocyanate groups contributes to these bands.

Khandar, Ali Akbar, E-mail: akhandar@yahoo.co [Department of Inorganic Chemistry, Faculty of Chemistry, University of Tabriz, 5166614766 Tabriz (Iran, Islamic Republic of); Klein, Axel [Institut fuer Anorganische Chemie, Universitaet zu Koeln, Greinstrasse 6, 50939 Koeln (Germany); Bakhtiari, Akbar [Department of Inorganic Chemistry, Faculty of Chemistry, University of Tabriz, 5166614766 Tabriz (Iran, Islamic Republic of); Institut fuer Anorganische Chemie, Universitaet zu Koeln, Greinstrasse 6, 50939 Koeln (Germany); Mahjoub, Ali Reza [Department of Chemistry, School of Science, Tarbiat Modares University, P.O. Box 14155-4838 Tehran (Iran, Islamic Republic of); Pohl, Roland W.H. [Institut fuer Anorganische Chemie, Universitaet zu Koeln, Greinstrasse 6, 50939 Koeln (Germany)

2011-02-15T23:59:59.000Z

72

Mercury CEM Calibration  

SciTech Connect (OSTI)

The Clean Air Mercury Rule (CAMR) which was published in the Federal Register on May 18, 2005, requires that calibration of mercury continuous emissions monitors (CEMs) be performed with NIST-traceable standards. Western Research Institute (WRI) is working closely with the Electric Power Research Institute (EPRI), the National Institute of Standards and Technology (NIST), and the Environmental Protection Agency (EPA) to facilitate the development of the experimental criteria for a NIST traceability protocol for dynamic elemental mercury vapor generators. The traceability protocol will be written by EPA. Traceability will be based on the actual analysis of the output of each calibration unit at several concentration levels ranging from about 2-40 ug/m{sup 3}, and this analysis will be directly traceable to analyses by NIST using isotope dilution inductively coupled plasma/mass spectrometry (ID ICP/MS) through a chain of analyses linking the calibration unit in the power plant to the NIST ID ICP/MS. Prior to this project, NIST did not provide a recommended mercury vapor pressure equation or list mercury vapor pressure in its vapor pressure database. The NIST Physical and Chemical Properties Division in Boulder, Colorado was subcontracted under this project to study the issue in detail and to recommend a mercury vapor pressure equation that the vendors of mercury vapor pressure calibration units can use to calculate the elemental mercury vapor concentration in an equilibrium chamber at a particular temperature. As part of this study, a preliminary evaluation of calibration units from five vendors was made. The work was performed by NIST in Gaithersburg, MD and Joe Rovani from WRI who traveled to NIST as a Visiting Scientist.

John F. Schabron; Joseph F. Rovani; Susan S. Sorini

2007-03-31T23:59:59.000Z

73

Paleomagnetic Secular Variation (PSV), 137Cs, and Hg dating techniques  

E-Print Network [OSTI]

Portland State University Department of Geology #12;Hg-Mercury contamination dating http fission of Uranium-235 · Due to nuclear weapons testing · Highly water soluble (spreads quickly) · Half

Fountain, Andrew G.

74

Electrolytic recovery of mercury enriched in isotopic abundance  

DOE Patents [OSTI]

The present invention is directed to a method of electrolytically extracting liquid mercury from HgO or Hg.sub.2 Cl.sub.2. Additionally there are disclosed two related techniques associated with the present invention, namely (1) a technique for selectively removing product from different regions of a long photochemical reactor (photoreactor) and (2) a method of accurately measuring the total quantity of mercury formed as either HgO or Hg.sub.2 Cl.sub.2.

Grossman, Mark W. (Belmont, MA)

1991-01-01T23:59:59.000Z

75

MODELING THE IMPACT OF ELEVATED MERCURY IN DEFENSE WASTE PROCESSING FACILITY MELTER FEED ON THE MELTER OFF-GAS SYSTEM - PRELIMINARY REPORT  

SciTech Connect (OSTI)

The Defense Waste Processing Facility (DWPF) is currently evaluating an alternative Chemical Process Cell (CPC) flowsheet to increase throughput. It includes removal of the steam-stripping step, which would significantly reduce the CPC processing time and lessen the sampling needs. However, its downside would be to send 100% of the mercury that come in with the sludge straight to the melter. For example, the new mercury content in the Sludge Batch 5 (SB5) melter feed is projected to be 25 times higher than that in the SB4 with nominal steam stripping of mercury. This task was initiated to study the impact of the worst-case scenario of zero-mercury-removal in the CPC on the DWPF melter off-gas system. It is stressed that this study is intended to be scoping in nature, so the results presented in this report are preliminary. In order to study the impact of elevated mercury levels in the feed, it is necessary to be able to predict how mercury would speciate in the melter exhaust under varying melter operating conditions. A homogeneous gas-phase oxidation model of mercury by chloride was developed to do just that. The model contains two critical parameters pertaining to the partitioning of chloride among HCl, Cl, Cl{sub 2}, and chloride salts in the melter vapor space. The values for these parameters were determined at two different melter vapor space temperatures by matching the calculated molar ratio of HgCl (or Hg{sub 2}Cl{sub 2}) to HgCl{sub 2} with those measured during the Experimental-Scale Ceramic Melter (ESCM) tests run at the Pacific Northwest National Laboratory (PNNL). The calibrated model was then applied to the SB5 simulant used in the earlier flowsheet study with an assumed mercury stripping efficiency of zero; the molar ratio of Cl-to-Hg in the resulting melter feed was only 0.4, compared to 12 for the ESCM feeds. The results of the model run at the indicated melter vapor space temperature of 650 C (TI4085D) showed that due to excessive shortage of chloride, only 6% of the mercury fed is expected to get oxidized, mostly as HgCl, while the remaining mercury would exist either as elemental mercury vapor (90%) or HgO (4%). Noting that the measured chloride level in the SB5 qualification sample was an order of magnitude lower than that used in the SB5 simulant, the degree of chloride shortage will be even greater. As a result, the projected level of HgCl in the actual SB5 melter exhaust will be even lower than 6% of the total mercury fed, while that of elemental mercury is likely to be greater than 90%. The homogeneous oxidation of mercury in the off-gas was deemed to be of primary importance based on the postulation that mercury and other volatile salts form submicron sized aerosols upon condensation and thus remain largely in the gas stream downstream of the quencher where they can deposit in the off-gas lines, Steam-Atomized Scrubbers (SAS), and High-Efficiency Mist Eliminator (HEME). Formation of these submicron semi-volatile salts in the condensate liquid is considered to be unlikely, so the liquid phase reactions were considered to be less important. However, subsequent oxidation of mercury in the liquid phase in the off-gas system was examined in a simplified model of the off-gas condensate. It was found that the condensate chemistry was consistent with further oxidation of elemental mercury to Hg{sub 2}Cl{sub 2} and conversion of HgO to chlorides. The results were consistent with the available experimental data. It should also be noted that the model predictions presented in this report do not include any physically entrained solids, which typically account for much of the off-gas carryover on a mass basis. The high elemental mercury vapor content predicted at the DWPF Quencher inlet means that physically entrained solids could provide the necessary surface onto which elemental mercury vapor could condense, thereby coating the solids as well as the internal surfaces of the off-gas system with mercury. Clearly, there are many process benefits to be gained by removing the steam-stripping step from the CPC c

Zamecnik, J.; Choi, A.

2009-03-25T23:59:59.000Z

76

MODELING THE IMPACT OF ELEVATED MERCURY IN DEFENSE WASTE PROCESSING FACILITY MELTER FEED ON THE MELTER OFF-GAS SYSTEM-PRELIMINARY REPORT  

SciTech Connect (OSTI)

The Defense Waste Processing Facility (DWPF) is currently evaluating an alternative Chemical Process Cell (CPC) flowsheet to increase throughput. It includes removal of the steam-stripping step, which would significantly reduce the CPC processing time and lessen the sampling needs. However, its downside would be to send 100% of the mercury that comes in with the sludge straight to the melter. For example, the new mercury content in the Sludge Batch 5 (SB5) melter feed is projected to be 25 times higher than that in the SB4 with nominal steam stripping of mercury. This task was initiated to study the impact of the worst-case scenario of zero-mercury-removal in the CPC on the DWPF melter offgas system. It is stressed that this study is intended to be scoping in nature, so the results presented in this report are preliminary. In order to study the impact of elevated mercury levels in the feed, it is necessary to be able to predict how mercury would speciate in the melter exhaust under varying melter operating conditions. A homogeneous gas-phase oxidation model of mercury by chloride was developed to do just that. The model contains two critical parameters pertaining to the partitioning of chloride among HCl, Cl, Cl{sub 2}, and chloride salts in the melter vapor space. The values for these parameters were determined at two different melter vapor space temperatures by matching the calculated molar ratio of HgCl (or Hg{sub 2}Cl{sub 2}) to HgCl{sub 2} with those measured during the Experimental-Scale Ceramic Melter (ESCM) tests run at the Pacific Northwest National Laboratory (PNNL). The calibrated model was then applied to the SB5 simulant used in the earlier flowsheet study with an assumed mercury stripping efficiency of zero; the molar ratio of Cl-to-Hg in the resulting melter feed was only 0.4, compared to 12 for the ESCM feeds. The results of the model run at the indicated melter vapor space temperature of 650 C (TI4085D) showed that due to excessive shortage of chloride, only 6% of the mercury fed is expected to get oxidized, mostly as HgCl, while the remaining mercury would exist either as elemental mercury vapor (90%) or HgO (4%). Noting that the measured chloride level in the SB5 qualification sample was an order of magnitude lower than that used in the SB5 simulant, the degree of chloride shortage will be even greater. As a result, the projected level of HgCl in the actual SB5 melter exhaust will be even lower than 6% of the total mercury fed, while that of elemental mercury is likely to be greater than 90%. The homogeneous oxidation of mercury in the off-gas was deemed to be of primary importance based on the postulation that mercury and other volatile salts form submicron sized aerosols upon condensation and thus remain largely in the gas stream downstream of the quencher where they can deposit in the off-gas lines, Steam-Atomized Scrubbers (SAS), and High-Efficiency Mist Eliminator (HEME). Formation of these submicron semi-volatile salts in the condensate liquid is considered to be unlikely, so the liquid phase reactions were considered to be less important. However, subsequent oxidation of mercury in the liquid phase in the off-gas system was examined in a simplified model of the off-gas condensate. It was found that the condensate chemistry was consistent with further oxidation of elemental mercury to Hg{sub 2}Cl{sub 2} and conversion of HgO to chlorides. The results were consistent with the available experimental data. It should also be noted that the model predictions presented in this report do not include any physically entrained solids, which typically account for much of the off-gas carryover on a mass basis. The high elemental mercury vapor content predicted at the DWPF Quencher inlet means that physically entrained solids could provide the necessary surface onto which elemental mercury vapor could condense, thereby coating the solids as well as the internal surfaces of the off-gas system with mercury. Clearly, there are many process benefits to be gained by removing the steam-stripping step from the CPC c

Zamecnik, J.; Choi, A.

2010-08-18T23:59:59.000Z

77

Argonne/EPA system captures mercury from air in gold shops |...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

the mercury vaporizes. The vaporized mercury is directed outside the shop into the open air where it descends onto homes, water and food of the local populations. Image credit:...

78

Mercury capture by aerosol transformation in combustion environments. Appendix 5  

SciTech Connect (OSTI)

Aerosol transformation of elemental mercury by oxidizing mercury in the air is investigated in this study by varying temperature and residence time. The experimental results show that mercury oxidation is not important at the temperature range and time scale studied. The rate of mercury oxidation is too slow that the capture of mercury vapor by transforming it into mercury oxide in aerosol phase is not practical in real systems. Studies are needed for alternative approaches to capture mercury vapor such as the use of sorbent materials.

NONE

1997-02-01T23:59:59.000Z

79

MERCURY CYCLING IN LAKE GORDON AND LAKE PEDDER, TASMANIA (AUSTRALIA). I: IN-LAKE PROCESSES  

E-Print Network [OSTI]

MERCURY CYCLING IN LAKE GORDON AND LAKE PEDDER, TASMANIA (AUSTRALIA). I: IN-LAKE PROCESSES KARL C; accepted 2 December 2002) Abstract. The processes affecting the concentrations of total mercury (total Hg- vestigated. Surface concentrations of total mercury (total Hg) were temporally and spatially uniform in both

Canberra, University of

80

Selenium inhibits the phytotoxicity of mercury in garlic (Allium sativum)  

SciTech Connect (OSTI)

To investigate the influence of selenium on mercury phytotoxicity, the levels of selenium and mercury were analyzed with inductively coupled plasma-mass spectrometry (ICP-MS) in garlic tissues upon exposure to different dosages of inorganic mercury (Hg{sup 2+}) and selenite (SeO{sub 3}{sup 2?}) or selenate (SeO{sub 4}{sup 2?}). The distributions of selenium and mercury were examined with micro-synchrotron radiation X-ray fluorescence (?-SRXRF), and the mercury speciation was investigated with micro-X-ray absorption near edge structure (?-XANES). The results show that Se at higher exposure levels (>1 mg/L of SeO{sub 3}{sup 2?} or SeO{sub 4}{sup 2?}) would significantly inhibit the absorption and transportation of Hg when Hg{sup 2+} levels are higher than 1 mg/L in culture media. SeO{sub 3}{sup 2?} and SeO{sub 4}{sup 2?} were found to be equally effective in reducing Hg accumulation in garlic. The inhibition of Hg uptake by Se correlates well with the influence of Se on Hg phytotoxicity as indicated by the growth inhibition factor. Elemental imaging using ?-SRXRF also shows that Se could inhibit the accumulation and translocation of Hg in garlic. ?-XANES analysis shows that Hg is mainly present in the forms of HgS bonding as Hg(GSH){sub 2} and Hg(Met){sub 2}. Se exposure elicited decrease of HgS bonding in the form of Hg(GSH){sub 2}, together with Se-mediated alteration of Hg absorption, transportation and accumulation, may account for attenuated Hg phytotoxicity by Se in garlic. -- Highlights: ? Hg phytotoxicity can be mitigated by Se supplement in garlic growth. ? Se can inhibit the accumulation and transportation of Hg in garlic tissues. ? Localization and speciation of Hg in garlic can be modified by Se.

Zhao, Jiating [CAS Key Laboratory of Nuclear Analytical Techniques, Key Lab for Biomedical Effects of Nanomaterial and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China)] [CAS Key Laboratory of Nuclear Analytical Techniques, Key Lab for Biomedical Effects of Nanomaterial and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); Gao, Yuxi, E-mail: gaoyx@ihep.ac.cn [CAS Key Laboratory of Nuclear Analytical Techniques, Key Lab for Biomedical Effects of Nanomaterial and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China)] [CAS Key Laboratory of Nuclear Analytical Techniques, Key Lab for Biomedical Effects of Nanomaterial and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); Li, Yu-Feng; Hu, Yi; Peng, Xiaomin [CAS Key Laboratory of Nuclear Analytical Techniques, Key Lab for Biomedical Effects of Nanomaterial and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China)] [CAS Key Laboratory of Nuclear Analytical Techniques, Key Lab for Biomedical Effects of Nanomaterial and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); Dong, Yuanxing [Department of Physics, Xinzhou Teachers University, Xinzhou 034000 (China)] [Department of Physics, Xinzhou Teachers University, Xinzhou 034000 (China); Li, Bai; Chen, Chunying [CAS Key Laboratory of Nuclear Analytical Techniques, Key Lab for Biomedical Effects of Nanomaterial and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China)] [CAS Key Laboratory of Nuclear Analytical Techniques, Key Lab for Biomedical Effects of Nanomaterial and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China); Chai, Zhifang, E-mail: chaizf@ihep.ac.cn [CAS Key Laboratory of Nuclear Analytical Techniques, Key Lab for Biomedical Effects of Nanomaterial and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China)] [CAS Key Laboratory of Nuclear Analytical Techniques, Key Lab for Biomedical Effects of Nanomaterial and Nanosafety, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing 100049 (China)

2013-08-15T23:59:59.000Z

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


81

Mercury Specie and Multi-Pollutant Control  

SciTech Connect (OSTI)

This project was awarded to demonstrate the ability to affect and optimize mercury speciation and multi-pollutant control using non-intrusive advanced sensor and optimization technologies. The intent was to demonstrate plant-wide optimization systems on a large coal fired steam electric power plant in order to minimize emissions, including mercury (Hg), while maximizing efficiency and maintaining saleable byproducts. Advanced solutions utilizing state-of-the-art sensors and neural network-based optimization and control technologies were proposed to maximize the removal of mercury vapor from the boiler flue gas thereby resulting in lower uncontrolled releases of mercury into the atmosphere. Budget Period 1 (Phase I) - Included the installation of sensors, software system design and establishment of the as-found baseline operating metrics for pre-project and post-project data comparison. Budget Period 2 (Phase II) - Software was installed, data communications links from the sensors were verified, and modifications required to integrate the software system to the DCS were performed. Budget Period 3 (Phase III) - Included the validation and demonstration of all control systems and software, and the comparison of the optimized test results with the targets established for the project site. This report represents the final technical report for the project, covering the entire award period and representing the final results compared to project goals. NeuCo shouldered 61% of the total project cost; while DOE shouldered the remaining 39%. The DOE requires repayment of its investment. This repayment will result from commercial sales of the products developed under the project. NRG's Limestone power plant (formerly owned by Texas Genco) contributed the host site, human resources, and engineering support to ensure the project's success.

Rob James; Virgil Joffrion; John McDermott; Steve Piche

2010-05-31T23:59:59.000Z

82

Natural mercury isotope variation in coal deposits and organic soils  

SciTech Connect (OSTI)

There is a need to distinguish among sources of Hg to the atmosphere in order to more fully understand global Hg pollution. In this study we investigate whether coal deposits within the United States, China, and Russia-Kazakhstan, which are three of the five greatest coal-producing regions, have diagnostic Hg isotopic fingerprints that can be used to discriminate among Hg sources. We also investigate the Hg isotopic composition of modern organic soil horizons developed in areas distant from point sources of Hg in North America. Mercury stored in coal deposits displays a wide range of both mass dependent fractionation and mass independent fractionation. {delta}{sup 202}Hg varies in coals by 3{per_thousand} and {Delta}{sup 201}Hg varies by 0.9{per_thousand}. Combining these two Hg isotope signals results in what may be a unique isotopic 'fingerprint' for many coal deposits. Mass independent fractionation of mercury has been demonstrated to occur during photochemical reactions of mercury. This suggests that Hg found in most coal deposits was subjected to photochemical reduction near the Earth's surface prior to deposition. The similarity in MDF and MIF of modern organic soils and coals from North America suggests that Hg deposition from coal may have imprinted an isotopic signature on soils. This research offers a new tool for characterizing mercury inputs from natural and anthropogenic sources to the atmosphere and provides new insights into the geochemistry of mercury in coal and soils. 35 refs., 2 figs., 1 tab.

Abir, Biswas; Joel D. Blum; Bridget A. Bergquist; Gerald J. Keeler; Zhouqing Xie [University of Michigan, Ann Arbor, MI (United States). Department of Geological Sciences

2008-11-15T23:59:59.000Z

83

Thief carbon catalyst for oxidation of mercury in effluent stream  

SciTech Connect (OSTI)

A catalyst for the oxidation of heavy metal contaminants, especially mercury (Hg), in an effluent stream is presented. The catalyst facilitates removal of mercury through the oxidation of elemental Hg into mercury (II) moieties. The active component of the catalyst is partially combusted coal, or "Thief" carbon, which can be pre-treated with a halogen. An untreated Thief carbon catalyst can be self-promoting in the presence of an effluent gas streams entrained with a halogen.

Granite, Evan J. (Wexford, PA); Pennline, Henry W. (Bethel Park, PA)

2011-12-06T23:59:59.000Z

84

Mercury Concentrations in Fish from the San Francisco Bay Area  

E-Print Network [OSTI]

Mercury Concentrations in Fish from the San Francisco Bay Area San Francisco Bay Regional Water on composite samples · Some mercury analysis on individual largemouth bass · Size targets #12;Tomales Bay Study chemical analyses (Hg and organics) conducted on composite samples · Some mercury analysis on individual

85

An assessment of methyl mercury and volatile mercury in land-applied sewage sludge  

SciTech Connect (OSTI)

In 1993, the US Environmental Protection Agency issued regulations covering the land-application of municipal sewage sludge. These regulations established maximum pollutant concentrations and were based upon a risk assessment of human exposure. Mercury, assumed to be inorganic and non-volatile, was one pollutant evaluated. From April, 1995 through February, 1996, the authors studied the species of mercury contaminating municipal sludge applied to land, and the potential for volatilization of mercury from land-applied sludge. Methyl mercury was found at 0.1% of total mercury concentrations and was emitted from land-applied sludge to the atmosphere. Elemental mercury (Hg) was formed in land-applied sludge via the reduction of oxidized mercury and was also emitted to the atmosphere. Hg emission from land-applied sludge was significantly elevated over background soil emission. Methyl mercury is more toxic and more highly bioaccumulated than inorganic mercury, and warrants assessment considering these special criteria. Additionally, mercury emission from sludge-amended soil may lead to the contamination of other environmental media with significant concentrations of the metal. Although these pathways were not evaluated in the regulatory risk assessment, they are an important consideration for evaluating the risks from mercury in land-applied sludge. This presentation will summarize the results of a re-assessment of US EPA regulations regarding the land-application of municipal sewage sludge using data on methyl mercury toxicity and mercury transport in the atmosphere.

Carpi, A. [Cornell Univ., Ithaca, NY (United States); Lindberg, S.E. [Oak Ridge National Lab., TN (United States)

1995-12-31T23:59:59.000Z

86

Mercury Chamber NF-IDS Meeting  

E-Print Network [OSTI]

-Battelle for the U.S. Department of Energy Mercury Chamber Update Oct 2011 Starting Point: Coil and Shielding Concept IDS120H #12;3 Managed by UT-Battelle for the U.S. Department of Energy Mercury Chamber Update Oct 2011 · Penetrations (ports) into chamber ­ Nozzle ­ Hg drains (overflow and maintenance) ­ Vents (in and out) ­ Beam

McDonald, Kirk

87

E-Print Network 3.0 - aluminum mercuric mercury Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

(II) mercuric mercury, doubly ionized (Hg2... . Mercury (among other heavy metals) is toxic to living organisms that have not de- veloped mechanisms... to cope with it. As one...

88

Lifestyle and Mercury Contamination of Amerindian Populations along the Beni River  

E-Print Network [OSTI]

1 Lifestyle and Mercury Contamination of Amerindian Populations along the Beni River (Lowland (Corresponding author), M.D., Ph.D. Abstract The objective of this paper was to document mercury contamination at the foothills of the Andes. Hair mercury content (H-Hg) served as a bioindicator of mercury contamination

Paris-Sud XI, Université de

89

Mercury Nozzle Status V.B. Graves  

E-Print Network [OSTI]

. DEPARTMENT OF ENERGY Hg Jet Design Meeting 15 Nov 2004 Flow Issues High flow in small diameter thin-wall 15 Nov 2004 Design Issues Desire mechanically attached nozzle for changeout during cold testingMercury Nozzle Status V.B. Graves Hg Jet Design Meeting Princeton University Nov 15, 2004 #12;OAK

McDonald, Kirk

90

Mercury Vapor | Open Energy Information  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's Heat JumpIncMAKGalwayHydrothermalMcFarlandSurvey Professional Paper Jump to:

91

Bioaccumulation of mercury in pelagic fishes in NW Gulf of Mexico  

E-Print Network [OSTI]

Total mercury (Hg) levels were determined in the tissues of ten taxa of pelagic fishes, with a special emphasis on apex predators (large vertebrates). Highest Hg levels were observed in blue marlin (Makaira nigricans), carcharhinid sharks (Genus...

Cai, Yan

2006-08-16T23:59:59.000Z

92

Environmental Toxicology INTER-AND INTRASPECIFIC VARIATION IN MERCURY BIOACCUMULATION BY SNAKES  

E-Print Network [OSTI]

--Reptiles Heavy metals Pollution Trophic position Stable isotopes INTRODUCTION Although the ecological value change, and environmental pollution [6]. Heavy metal contaminants such as mercury (Hg) are a major

Willson. J.D.

93

Note: Production of a mercury beam with an electron cyclotron resonance ion source  

SciTech Connect (OSTI)

An electron cyclotron resonance ion source has been utilized to produce mercury beams with intensities of 4.5 e?A of {sup 202}Hg{sup 29+} and 3.0 e?A of {sup 202}Hg{sup 31+} from natural abundance mercury metal. The production technique relies on the evaporation of liquid mercury into the source plasma vacuum region and utilizes elemental mercury instead of a volatile organic compound as the neutral feed material.

Vondrasek, R.; Pardo, R.; Scott, R. [Physics Division, Argonne National Laboratory, Lemont, Illinois 60439 (United States)] [Physics Division, Argonne National Laboratory, Lemont, Illinois 60439 (United States)

2013-11-15T23:59:59.000Z

94

Mercury Emission Control Technologies for PPL Montana-Colstrip Testing  

SciTech Connect (OSTI)

The Energy & Environmental Research Center (EERC) was asked by PPL Montana LLC (PPL) to provide assistance and develop an approach to identify cost-effective options for mercury control at its coal-fired power plants. The work conducted focused on baseline mercury level and speciation measurement, short-term parametric testing, and week long testing of mercury control technology at Colstrip Unit 3. Three techniques and various combinations of these techniques were identified as viable options for mercury control. The options included oxidizing agents or sorbent enhancement additives (SEAs) such as chlorine-based SEA1 and an EERC proprietary SEA2 with and without activated carbon injection. Baseline mercury emissions from Colstrip Unit 3 are comparatively low relative to other Powder River Basin (PRB) coal-fired systems and were found to range from 5 to 6.5 g/Nm3 (2.9 to 3.8 lb/TBtu), with a rough value of approximately 80% being elemental upstream of the scrubber and higher than 95% being elemental at the outlet. Levels in the stack were also greater than 95% elemental. Baseline mercury removal across the scrubber is fairly variable but generally tends to be about 5% to 10%. Parametric results of carbon injection alone yielded minimal reduction in Hg emissions. SEA1 injection resulted in 20% additional reduction over baseline with the maximum rate of 400 ppm (3 gal/min). Week long testing was conducted with the combination of SEA2 and carbon, with injection rates of 75 ppm (10.3 lb/hr) and 1.5 lb/MMacf (40 lb/hr), respectively. Reduction was found to be an additional 30% and, overall during the testing period, was measured to be 38% across the scrubber. The novel additive injection method, known as novel SEA2, is several orders of magnitude safer and less expensive than current SEA2 injection methods. However, used in conjunction with this plant configuration, the technology did not demonstrate a significant level of mercury reduction. Near-future use of this technique at Colstrip is not seen. All the additives injected resulted in some reduction in mercury emissions. However, the target reduction of 55% was not achieved. The primary reason for the lower removal rates is because of the lower levels of mercury in the flue gas stream and the lower capture level of fine particles by the scrubbers (relative to that for larger particles). The reaction and interaction of the SEA materials is with the finer fraction of the fly ash, because the SEA materials are vaporized during the combustion or reaction process and condense on the surfaces of entrained particles or form very small particles. Mercury will have a tendency to react and interact with the finer fraction of entrained ash and sorbent as a result of the higher surface areas of the finer particles. The ability to capture the finer fraction of fly ash is the key to controlling mercury. Cost estimates for mercury removal based on the performance of each sorbent during this project are projected to be extremely high. When viewed on a dollar-per-pound-of-mercury removed basis activated carbon was projected to cost nearly $1.2 million per pound of mercury removed. This value is roughly six times the cost of other sorbent-enhancing agents, which were projected to be closer to $200,000 per pound of mercury removed.

John P. Kay; Michael L. Jones; Steven A. Benson

2007-04-01T23:59:59.000Z

95

Surface properties of liquid mercury: a comparison of density-dependent and density-independent force fields  

E-Print Network [OSTI]

The surface properties of liquid mercury (Hg) at a temperature of 293 K are investigated by classical Molecular Dynamics simulation using density-independent (DI) and density-dependent (DD) force fields. The latter force fields were introduced to improve the description of surface properties. Both force fields yield lower values of the surface tension in comparison to experimental data. Moreover, the density-dependent force field results in an anomalous thermodynamic behavior. These findings are rationalized by liquid-state theory. An optimized, density-independent force field is proposed that yields a higher surface tension and, at the same time, provides an accurate description of the liquid-vapor coexistence.

A. Iakovlev; D. Bedrov; M. Mller

2014-12-08T23:59:59.000Z

96

Method for isotope enrichment of mercury-196 by selective photoionization  

DOE Patents [OSTI]

A method is provided for selectively photoionizing .sup.196 Hg atoms in a vapor utilizing a three or four-step photoionization process.

Paisner, Jeffrey A. (San Ramon, CA); Crane, John K. (Pleasanton, CA)

1988-01-01T23:59:59.000Z

97

Mercury toxicokinetics-dependency on strain and gender  

SciTech Connect (OSTI)

Mercury (Hg) exposure from dental amalgam fillings and thimerosal in vaccines is not a major health hazard, but adverse health effects cannot be ruled out in a small and more susceptible part of the exposed population. Individual differences in toxicokinetics may explain susceptibility to mercury. Inbred, H-2-congenic A.SW and B10.S mice and their F1- and F2-hybrids were given HgCl{sub 2} with 2.0 mg Hg/L drinking water and traces of {sup 203}Hg. Whole-body retention (WBR) was monitored until steady state after 5 weeks, when the organ Hg content was assessed. Despite similar Hg intake, A.SW males attained a 20-30% significantly higher WBR and 2- to 5-fold higher total renal Hg retention/concentration than A.SW females and B10.S mice. A selective renal Hg accumulation but of lower magnitude was seen also in B10.S males compared with females. Differences in WBR and organ Hg accumulation are therefore regulated by non-H-2 genes and gender. Lymph nodes lacked the strain- and gender-dependent Hg accumulation profile of kidney, liver and spleen. After 15 days without Hg A.SW mice showed a 4-fold higher WBR and liver Hg concentration, but 11-fold higher renal Hg concentration, showing the key role for the kidneys in explaining the slower Hg elimination in A.SW mice. The trait causing higher mercury accumulation was not dominantly inherited in the F1 hybrids. F2 mice showed a large inter-individual variation in Hg accumulation, showing that multiple genetic factors influence the Hg toxicokinetics in the mouse. The genetically heterogeneous human population may therefore show a large variation in mercury toxicokinetics.

Ekstrand, Jimmy [Molecular and Immunological Pathology, Department of Clinical and Experimental Medicine, Linkoeping University, SE-581 85 Linkoeping (Sweden); Nielsen, Jesper B. [Department of Environmental Medicine, University of Southern Denmark, DK-5000 Odense C (Denmark); Havarinasab, Said [Molecular and Immunological Pathology, Department of Clinical and Experimental Medicine, Linkoeping University, SE-581 85 Linkoeping (Sweden); Zalups, Rudolfs K. [Division of Basic Medical Sciences, Mercer University School of Medicine, 1550 College Street, Macon, GA 31207 (United States); Soederkvist, Peter [Cell Biology, Department of Clinical and Experimental Medicine, Linkoeping University, SE-581 85 Linkoeping (Sweden); Hultman, Per, E-mail: perhu@imk.liu.s [Molecular and Immunological Pathology, Department of Clinical and Experimental Medicine, Linkoeping University, SE-581 85 Linkoeping (Sweden)

2010-03-15T23:59:59.000Z

98

Mercury CEM Calibration  

SciTech Connect (OSTI)

Mercury continuous emissions monitoring systems (CEMS) are being implemented in over 800 coal-fired power plant stacks. The power industry desires to conduct at least a full year of monitoring before the formal monitoring and reporting requirement begins on January 1, 2009. It is important for the industry to have available reliable, turnkey equipment from CEM vendors. Western Research Institute (WRI) is working closely with the Electric Power Research Institute (EPRI), the National Institute of Standards and Technology (NIST), and the Environmental Protection Agency (EPA) to facilitate the development of the experimental criteria for a NIST traceability protocol for dynamic elemental mercury vapor generators. The generators are used to calibrate mercury CEMs at power plant sites. The Clean Air Mercury Rule (CAMR) which was published in the Federal Register on May 18, 2005 requires that calibration be performed with NIST-traceable standards (Federal Register 2007). Traceability procedures will be defined by EPA. An initial draft traceability protocol was issued by EPA in May 2007 for comment. In August 2007, EPA issued an interim traceability protocol for elemental mercury generators (EPA 2007). The protocol is based on the actual analysis of the output of each calibration unit at several concentration levels ranging initially from about 2-40 {micro}g/m{sup 3} elemental mercury, and in the future down to 0.2 {micro}g/m{sup 3}, and this analysis will be directly traceable to analyses by NIST. The document is divided into two separate sections. The first deals with the qualification of generators by the vendors for use in mercury CEM calibration. The second describes the procedure that the vendors must use to certify the generator models that meet the qualification specifications. The NIST traceable certification is performance based, traceable to analysis using isotope dilution inductively coupled plasma/mass spectrometry performed by NIST in Gaithersburg, MD. The outputs of mercury generators are compared to one another using a nesting procedure which allows direct comparison of one generator with another and eliminates analyzer variability effects. The qualification portion of the EPA interim traceability protocol requires the vendors to define generator performance as affected by variables such as pressure, temperature, line voltage, and shipping. WRI is focusing efforts to determine actual generator performance related to the variables defined in the qualification portion of the interim protocol. The protocol will then be further revised by EPA based on what can actually be achieved with the generators. Another focus of the study is to evaluate approaches for field verification of generator performance. Upcoming work includes evaluation of oxidized mercury calibration generators, for which a separate protocol will be prepared by EPA. In addition, the variability of the spectrometers/analyzers under various environmental conditions needs to be defined and understood better. A main objective of the current work is to provide data on the performance and capabilities of elemental mercury generator/calibration systems for the development of realistic NIST traceability protocols for mercury vapor standards for continuous emission CEM calibration. This work is providing a direct contribution to the enablement of continuous emissions monitoring at coal-fired power plants in conformance with the CAMR. EPA Specification 12 states that mercury CEMs must be calibrated with NIST-traceable standards (Federal Register 2005). The initial draft of an elemental mercury generator traceability protocol was circulated by EPA in May 2007 for comment, and an interim protocol was issued in August 2007 (EPA 2007). Initially it was assumed that the calibration and implementation of mercury CEMs would be relatively simple, and implementation would follow the implementation of the Clean Air Interstate Rule (CAIR) SO{sub 2} and NO{sub x} monitoring, and sulfur emissions cap and trade. However, mercury has proven to be significantly more difficult

John Schabron; Joseph Rovani; Mark Sanderson

2008-02-29T23:59:59.000Z

99

Coadsorption of sulfate/bisulfate anions with Hg cations during Hg underpotential deposition on Au(111): An in situ x-ray diffraction study  

SciTech Connect (OSTI)

The first stage of mercury underpotential deposition on Au(111) electrodes in 0.10 M H{sub 2}SO{sub 4} containing 1.0 mM Hg{sup 2+} has been studied by synchrotron X-ray scattering techniques including grazing incidence X-ray diffraction and specular crystal truncation rod measurements. An ordered coadsorbed structure of sulfate/bisulfate anions and Hg cations was found at potentials between the first and second Hg UPD peaks (+0.80 V > E > +0.88 V vs Ag/AgCl(3 M KCl)). The coadsorption structure was found to consist of a compressed Hg honeycomb lattice with the honeycomb centers occupied by sulfate or bisulfate anions. The compression of the lattice is likely due to the formation of mercurous (Hg{sub 2}{sup 2+}) ions which have a much shorter Hg-Hg distance than that in frozen bulk Hg crystals. The net charge transferred under the first Hg UPD peak suggests that the chemical state of the species in the coadsorbed structure is likely Hg{sub 2}SO{sub 4}. Our results indicate that both the chemical state of the mercury cations and the nature of the anions are important in the resulting electrodeposited structures. 38 refs., 8 figs., 1 tab.

Li, J.; Abruna, H.D. [Cornell Univ., Ithaca, NY (United States)] [Cornell Univ., Ithaca, NY (United States)

1997-01-09T23:59:59.000Z

100

Mercury Isotope Fractionation by Environmental Transport and Transformation Processes  

E-Print Network [OSTI]

measuring Hg 0 that permeated PVC tubing and matching this26 Chapter 3 Elemental Mercury Diffusion in a PVC29 Figure 3.2 The setup for diffusion in PVC

Koster van Groos, Paul Gijsbert

2011-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


101

Transformations of mercury in the marine water column  

E-Print Network [OSTI]

Methylation of mercury (Hg) in the marine water column has been hypothesized to serve as the primary source of the bioaccumulating chemical species monomethylmercury (MMHg) to marine food webs. Despite decades of research ...

Munson, Kathleen M. (Kathleen May)

2014-01-01T23:59:59.000Z

102

Thiacrown polymers for removal of mercury from waste streams  

DOE Patents [OSTI]

Thiacrown polymers immobilized to a polystyrene-divinylbenzene matrix react with Hg.sup.2+ under a variety of conditions to efficiently and selectively remove Hg.sup.2+ ions from acidic aqueous solutions, even in the presence of a variety of other metal ions. The mercury can be recovered and the polymer regenerated. This mercury removal method has utility in the treatment of industrial wastewater, where a selective and cost-effective removal process is required.

Baumann, Theodore F. (Tracy, CA); Reynolds, John G. (San Ramon, CA); Fox, Glenn A. (Livermore, CA)

2002-01-01T23:59:59.000Z

103

Mercury Contamination in Pelagic Fishes of the Gulf of Mexico  

E-Print Network [OSTI]

2 Map of sampling locations at the docks and offshore from ` Freeport and Port Aransas, Texas, and Venice, Louisiana, in the NW of Gulf of Mexico. .................................................................... 11 3 Mean Hg concentration...). Figure 1 Mercury cycling and bioaccumulation in aquatic system (Engstrom 2007). Elemental Hg can be oxidized by chemical reactions that depend on ozone, solar energy and water content in the atmosphere. Mercury oxidation is a photochemical 6...

Kuklyte, Ligita

2012-10-19T23:59:59.000Z

104

Final Project Report: "??Exploratory Research: Mercury Stable Isotopes as Indicators of the Biogeochemical Cycling of Mercury"?  

SciTech Connect (OSTI)

This is the final project report for award DE-SC0005351, which supported the research project "??Exploratory Research: Mercury Stable Isotopes as Indicators of the Biogeochemical Cycling of Mercury."? This exploratory project investigated the use of mercury (Hg) stable isotope measurements as a new approach to study how Hg moves and changes its chemical form in environmental systems, with particular focus on the East Fork of Poplar Creek (EFPC) near the DOE Y-12 plant (a Hg contamination source). This study developed analytical methods and collected pilot data that have set the stage for more detailed studies and have begun to provide insights into Hg movement and chemical changes. The overall Hg stable isotope approach was effective. The Hg isotope analysis methods yielded high-precision measurements of the sediment, water, and fish samples analyzed; quality control measures demonstrated the precision. The pilot data show that the 202Hg/198Hg, 199Hg/198Hg, and 201Hg/198Hg isotope ratios vary in this system. 202Hg/198Hg ratios of the Hg released from the Y-12 plant are relatively high, and those of the regional Hg background in soils and river sediments are significantly lower. Unfortunately, 202Hg/198Hg differences that might have been useful to distinguish early Hg releases from later releases were not observed. However, 202Hg/198Hg ratios in sediments do provide insights into chemical transformations that may occur as Hg moves through the system. Furthermore, 199Hg/198Hg and 201Hg/198Hg ratio analyses of fish tissues indicate that the effects of sunlight-driven chemical reactions on the Hg that eventually ends up in EFPC fish are measureable, but small. These results provide a starting point for a more detailed study (already begun at Univ. of Michigan) that will continue Hg isotope ratio work aimed at improving understanding of how Hg moves, changes chemically, and does or does not take on more highly toxic forms in the Oak Ridge area. This work also benefits efforts to trace Hg contamination in the Clinch and Tennessee Rivers, into which EFPC flows, and to distinguish Hg from the Y-12 plant from that released from a nearby coal ash accident.

Johnson, Thomas M

2012-08-01T23:59:59.000Z

105

Method for combined removal of mercury and nitrogen oxides from off-gas streams  

DOE Patents [OSTI]

A method for removing elemental Hg and nitric oxide simultaneously from a gas stream is provided whereby the gas stream is reacted with gaseous chlorinated compound to convert the elemental mercury to soluble mercury compounds and the nitric oxide to nitrogen dioxide. The method works to remove either mercury or nitrogen oxide in the absence or presence of each other.

Mendelsohn, Marshall H. (Downers Grove, IL); Livengood, C. David (Lockport, IL)

2006-10-10T23:59:59.000Z

106

Methylation of Mercury by Bacteria Exposed to Dissolved, Nanoparticulate, and Microparticulate Mercuric Sulfides  

E-Print Network [OSTI]

Methylation of Mercury by Bacteria Exposed to Dissolved, Nanoparticulate, and Microparticulate in the environment is partly controlled by the bioavailability of inorganic divalent mercury (Hg(II)) to anaerobic matter to form chemical species that include organic-coated mercury sulfide nanoparticles as reaction

107

Mercury and Sulfur Dynamics in the SPRUCE Experiment Brandy Toner1  

E-Print Network [OSTI]

Mercury and Sulfur Dynamics in the SPRUCE Experiment Brandy Toner1 , Randy Kolka2 , Steve Sebestyen will lead studies assessing the influence of SPRUCE treatments on the cycling of THg, MeHg and S. Mercury. Mercury levels are determined by complex interactions between deposition, chemical transformation

108

Changes in mercury bioaccumulation in an apex predator in response to removal of an introduced competitor  

E-Print Network [OSTI]

Changes in mercury bioaccumulation in an apex predator in response to removal of an introduced and decreased mercury concentrations in remaining fish. Instead, we observed a significant increase in lake web structure can influence MeHg concentrations in top predators. Keywords Mercury Á Food web Á Fish

Kraft, Clifford E.

109

WDM school, January 14, 2008 Equation of State for Fluid Mercury  

E-Print Network [OSTI]

1 WDM school, January 14, 2008 Equation of State for Fluid Mercury Based on Interatomic Many, Fluid Metals (Princeton, 1999) elements Tc (K) Pc (bar) c (g/cm3) Mercury (Hg) Cesium (Cs) Rubidium (Rb.30 divalent monovalent (alkali) Importance of mercury -- lowest critical temperature -- critical point

110

Atmospheric Mercury in the Great Lakes Region An Evaluation of the Community Multiscale Air Quality  

E-Print Network [OSTI]

Atmospheric Mercury in the Great Lakes Region An Evaluation of the Community Multiscale Air Quality Tracey Holloway #12;i Abstract Atmospheric mercury is a significant source for methylmercury (Me. In order to control MeHg exposures, policy-makers need a clear understanding of the atmospheric mercury

Wisconsin at Madison, University of

111

Mercury Dynamics in a San Francisco Estuary Tidal Wetland: Assessing Dynamics Using In Situ Measurements  

E-Print Network [OSTI]

Mercury Dynamics in a San Francisco Estuary Tidal Wetland: Assessing Dynamics Using In Situ the tidally driven exchange of mercury (Hg) between the waters of the San Francisco estuary and Browns Island, respectively--together predicted 94 % of the observed variability in measured total mercury concentra- tion

Boss, Emmanuel S.

112

The Sulfate-Reducing Bacterium Desulfovibrio desulfuricans ND132 as a Model for Understanding Bacterial Mercury  

E-Print Network [OSTI]

Bacterial Mercury Methylation Contact: Cynthia Gilmour (gilmourc@si.edu, 443-482-2498) DOE/Office of Science/Biological & Environmental Research ·The ORNL Mercury Science Focus Area is developing the Hg-methylating bacterium as a model for understanding bacterial mercury methylation. Appl. Environ. Microbiol. 77:3938-3951 (doi:10

113

Mercury contaminated sediment sitesAn evaluation of remedial options  

SciTech Connect (OSTI)

Mercury (Hg) is a naturally-occurring element that is ubiquitous in the aquatic environment. Though efforts have been made in recent years to decrease Hg emissions, historically-emitted Hg can be retained in the sediments of aquatic bodies where they may be slowly converted to methylmercury (MeHg). Consequently, Hg in historically-contaminated sediments can result in high levels of significant exposure for aquatic species, wildlife and human populations consuming fish. Even if source control of contaminated wastewater is achievable, it may take a very long time, perhaps decades, for Hg-contaminated aquatic systems to reach relatively safe Hg levels in both water and surface sediment naturally. It may take even longer if Hg is present at higher concentration levels in deep sediment. Hg contaminated sediment results from previous releases or ongoing contributions from sources that are difficult to identify. Due to human activities or physical, chemical, or biological processes (e.g. hydrodynamic flows, bioturbation, molecular diffusion, and chemical transformation), the buried Hg can be remobilized into the overlying water. Hg speciation in the water column and sediments critically affect the reactivity (i.e. conversion of inorganic Hg(II) to MeHg), transport, and its exposure to living organisms. Also, geochemical conditions affect the activity of methylating bacteria and its availability for methylation. This review paper discusses remedial considerations (e.g. key chemical factors in fate and transport of Hg, source characterization and control, environmental management procedures, remediation options, modeling tools) and includes practical case studies for cleaning up Hg-contaminated sediment sites. -- Highlights: ? Managing mercury-contaminated sediment sites are challenging to remediate. ? Remediation technologies are making a difference in managing these sites. ? Partitioning plays a dominant role in the distribution of mercury species. ? Mathematical models can be used to help us understand the chemistry and processes.

Randall, Paul M., E-mail: randall.paul@epa.gov [U.S. Environmental Protection Agency, Office of Research and Development, National Risk Management Research Laboratory, 26 West Martin Luther King Drive, Cincinnati, OH 45268 (United States); Chattopadhyay, Sandip, E-mail: Sandip.Chattopadhyay@tetratech.com [Tetra Tech, Inc., 250 West Court Street, Suite 200W, Cincinnati, OH 45202 (United States)] [Tetra Tech, Inc., 250 West Court Street, Suite 200W, Cincinnati, OH 45202 (United States)

2013-08-15T23:59:59.000Z

114

Fluorescent sensor for mercury  

DOE Patents [OSTI]

The present invention provides a sensor for detecting mercury, comprising: a first polynucleotide, comprising a first region, and a second region, a second polynucleotide, a third polynucleotide, a fluorophore, and a quencher, wherein the third polynucleotide is optionally linked to the second region; the fluorophore is linked to the first polynucleotide and the quencher is linked to the second polynucleotide, or the fluorophore is linked to the second polynucleotide and the quencher is linked to the first polynucleotide; the first region and the second region hybridize to the second polynucleotide; and the second region binds to the third polynucleotide in the presence of Hg.sup.2+ ions.

Wang, Zidong (Urbana, IL); Lee, Jung Heon (Evanston, IL); Lu, Yi (Champaign, IL)

2011-11-22T23:59:59.000Z

115

Mercury removal in utility wet scrubber using a chelating agent  

DOE Patents [OSTI]

A method for capturing and reducing the mercury content of an industrial flue gas such as that produced in the combustion of a fossil fuel or solid waste adds a chelating agent, such as ethylenediaminetetraacetic acid (EDTA) or other similar compounds like HEDTA, DTPA and/or NTA, to the flue gas being scrubbed in a wet scrubber used in the industrial process. The chelating agent prevents the reduction of oxidized mercury to elemental mercury, thereby increasing the mercury removal efficiency of the wet scrubber. Exemplary tests on inlet and outlet mercury concentration in an industrial flue gas were performed without and with EDTA addition. Without EDTA, mercury removal totaled 42%. With EDTA, mercury removal increased to 71%. The invention may be readily adapted to known wet scrubber systems and it specifically provides for the removal of unwanted mercury both by supplying S.sup.2- ions to convert Hg.sup.2+ ions into mercuric sulfide (HgS) and by supplying a chelating agent to sequester other ions, including but not limited to Fe.sup.2+ ions, which could otherwise induce the unwanted reduction of Hg.sup.2+ to the form, Hg.sup.0.

Amrhein, Gerald T. (Louisville, OH)

2001-01-01T23:59:59.000Z

116

Emission and Long-Range Transport of Gaseous Mercury from a  

E-Print Network [OSTI]

Emission and Long-Range Transport of Gaseous Mercury from a Large-Scale Canadian Boreal Forest FireQuebec.Thesemeasurementsindicated significant and highly correlated increases in Hg and CO during the plume event. The Hg:CO emissions ratio emissions and biomass burned to determine a mean area-based Hg emission flux density for boreal forest fires

Lee, Xuhui

117

UNCERTAINTY IN PALEOECOLOGICAL STUDIES OF MERCURY IN SEDIMENT CORES  

E-Print Network [OSTI]

and required corrections for remaining water content. Frozen sediments did not lose Hg during a 72-day storage of the analysis (while adhering to strict QA/QC criteria) produced compounded uncertainties of ±11 and ±29% in Hg to correctly evaluate trends and remediation efforts. Keywords: Florida Everglades, Lake Erie, mercury

Gottgens, Hans

118

Mercury emission behavior during isolated coal particle combustion  

E-Print Network [OSTI]

ppb and 140ppb. In order to understand the basic process of formulation of HgCl2 and Hg0 a numerical model is developed in the current work to simulate in the detail i) heating ii) transient pyrolysis of coal and evolution of mercury and chlorine, iii...

Puchakayala, Madhu Babu

2009-05-15T23:59:59.000Z

119

Method of preparing mercury with an arbitrary isotopic distribution  

DOE Patents [OSTI]

This invention provides for a process for preparing mercury with a predetermined, arbitrary, isotopic distribution. In one embodiment, different isotopic types of Hg[sub 2]Cl[sub 2], corresponding to the predetermined isotopic distribution of Hg desired, are placed in an electrolyte solution of HCl and H[sub 2]O. The resulting mercurous ions are then electrolytically plated onto a cathode wire producing mercury containing the predetermined isotopic distribution. In a similar fashion, Hg with a predetermined isotopic distribution is obtained from different isotopic types of HgO. In this embodiment, the HgO is dissolved in an electrolytic solution of glacial acetic acid and H[sub 2]O. The isotopic specific Hg is then electrolytically plated onto a cathode and then recovered. 1 fig.

Grossman, M.W.; George, W.A.

1986-12-16T23:59:59.000Z

120

Method of preparing mercury with an arbitrary isotopic distribution  

DOE Patents [OSTI]

This invention provides for a process for preparing mercury with a predetermined, arbitrary, isotopic distribution. In one embodiment, different isotopic types of Hg.sub.2 Cl.sub.2, corresponding to the predetermined isotopic distribution of Hg desired, are placed in an electrolyte solution of HCl and H.sub.2 O. The resulting mercurous ions are then electrolytically plated onto a cathode wire producing mercury containing the predetermined isotopic distribution. In a similar fashion, Hg with a predetermined isotopic distribution is obtained from different isotopic types of HgO. In this embodiment, the HgO is dissolved in an electrolytic solution of glacial acetic acid and H.sub.2 O. The isotopic specific Hg is then electrolytically plated onto a cathode and then recovered.

Grossman, Mark W. (Belmont, MA); George, William A. (Rockport, MA)

1986-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


121

Mercury Methylation at Mercury Mines In The Humboldt River Basin, Nevada, USA  

SciTech Connect (OSTI)

Total Hg and methylmercury concentrations were measured in mine-waste calcines (retorted ore), sediment, and water samples collected in and around abandoned mercury mines in western Nevada to evaluate Hg methylation at the mines and in the Humboldt River basin. Mine-waste calcines contain total Hg concentrations as high as 14 000?g/g. Stream-sediment samples collected within 1 km of the mercury mines contain total Hg concentrations as high as 170?g/g, whereas stream sediments collected>5 km from the mines, and those collected from the Humboldt River and regional baseline sites, contain total Hg concentrations<0.5?g/g. Similarly, methylmercury concentrations in mine-waste calcines are locally as high as 96 ng/g, but methylmercury contents in stream-sediments collected downstream from the mines and from the Humboldt River are lower, ranging from<0.05 to 0.95 ng/g. Stream-water samples collected below two mines studied contain total Hg concentrations ranging from 6 to 2000 ng/L, whereas total Hg in Humboldt River water was generally lower ranging from 2.1 to 9.0 ng/L. Methylmercury concentrations in the Humboldt River water were the lowest in this study (<0.02-0.27 ng/L). Although total Hg and methylmercury concentrations are locally high in mine-waste calcines, there is significant dilution of Hg and lower Hg methylation down gradient from the mines, especially in the sediments and water collected from the Humboldt River, which is> 8 km from any mercury mines. Our data indicate little transference of Hg and methylmercury from the sediment to the water column due to the lack of mine runoff in this desert climate.

Gray, John E. (U.S. Geological Survey); Crock, James G. (U.S. Geological Survey); Lasorsa, Brenda K. (BATTELLE (PACIFIC NW LAB))

2002-12-01T23:59:59.000Z

122

Mercury Spills EHS Contact: Kate Lumley-Sapanski (kxl3@psu.edu) 814-865-6391  

E-Print Network [OSTI]

Mercury Spills EHS Contact: Kate Lumley-Sapanski (kxl3@psu.edu) 814-865-6391 Michael Burke (mjb7 Not Enter ­Mercury Spill" · Call EHS immediately When to Report: For large mercury spills (i.e. manometers) or spills in areas where loose mercury could be heated (>90 F degrees) and vapors released and call EHS

Maroncelli, Mark

123

Mercury emissions from municipal solid waste combustors  

SciTech Connect (OSTI)

This report examines emissions of mercury (Hg) from municipal solid waste (MSW) combustion in the United States (US). It is projected that total annual nationwide MSW combustor emissions of mercury could decrease from about 97 tonnes (1989 baseline uncontrolled emissions) to less than about 4 tonnes in the year 2000. This represents approximately a 95 percent reduction in the amount of mercury emitted from combusted MSW compared to the 1989 mercury emissions baseline. The likelihood that routinely achievable mercury emissions removal efficiencies of about 80 percent or more can be assured; it is estimated that MSW combustors in the US could prove to be a comparatively minor source of mercury emissions after about 1995. This forecast assumes that diligent measures to control mercury emissions, such as via use of supplemental control technologies (e.g., carbon adsorption), are generally employed at that time. However, no present consensus was found that such emissions control measures can be implemented industry-wide in the US within this time frame. Although the availability of technology is apparently not a limiting factor, practical implementation of necessary control technology may be limited by administrative constraints and other considerations (e.g., planning, budgeting, regulatory compliance requirements, etc.). These projections assume that: (a) about 80 percent mercury emissions reduction control efficiency is achieved with air pollution control equipment likely to be employed by that time; (b) most cylinder-shaped mercury-zinc (CSMZ) batteries used in hospital applications can be prevented from being disposed into the MSW stream or are replaced with alternative batteries that do not contain mercury; and (c) either the amount of mercury used in fluorescent lamps is decreased to an industry-wide average of about 27 milligrams of mercury per lamp or extensive diversion from the MSW stream of fluorescent lamps that contain mercury is accomplished.

Not Available

1993-05-01T23:59:59.000Z

124

Assessing the Risk of Mercury in Drinking Water after UV Lamp Breaks Page 1 Assessing the Risk of Mercury in Drinking Water after UV Lamp Breaks  

E-Print Network [OSTI]

Assessing the Risk of Mercury in Drinking Water after UV Lamp Breaks Page 1 Assessing the Risk of Mercury in Drinking Water after UV Lamp Breaks Heidi Borchers University of New Hampshire, Environmental Ultraviolet (UV) lamps generate ultraviolet light through the vaporization of elemental mercury, by using

125

REDUCTION OF INHERENT MERCURY EMISSIONS IN PC COMBUSTION  

SciTech Connect (OSTI)

Oxidized mercury has been shown to be more easily removed from power plant flue gas by existing air pollution control equipment (e.g., wet scrubbers) than elemental mercury. The factors that determine how mercury is converted to the oxidized form in practical systems are, however, unknown. The present research focuses on developing an elementary, homogeneous mechanism that describes the oxidation of mercury by chlorine species as it occurs in practical furnaces. The goal is to use this mechanism (1) as a component in an overall homogeneous/heterogeneous mechanism that describes mercury behavior, and (2) to suggest low cost/low impact means of promoting mercury oxidation in furnaces. The results suggest an important role for Hg+Cl {r_arrow} HgCl and HgCl + Cl {r_arrow} HgCl{sub 2}. Here, the Cl is derived by radical attack on HCl in the high-temperature environment. The results suggest that the oxidation occurs during the time that the gases cool to room temperature. The high Cl concentrations from the flame persist into the quench region and provide for the oxidation of Hg to HgCl{sub 2} under lower temperatures where the products are stable. Under this mechanism, no significant HgCl{sub 2} is actually present at the higher temperatures where oxidized mercury is often reported in the literature (e.g., 900 C). Instead, all oxidation occurs as these gases are quenched. The results suggest that means of promoting Cl concentrations in the furnace will increase oxidation.

John C. Kramlich; Rebecca N. Sliger

2000-08-26T23:59:59.000Z

126

Method and apparatus to measure vapor pressure in a flow system  

DOE Patents [OSTI]

The present invention is directed to a method for determining, by a condensation method, the vapor pressure of a material with a known vapor pressure versus temperature characteristic, in a flow system particularly in a mercury isotope enrichment process.

Grossman, Mark W. (Belmont, MA); Biblarz, Oscar (Swampscott, MA)

1991-01-01T23:59:59.000Z

127

Process of [sup 196]Hg enrichment  

DOE Patents [OSTI]

A simple rate equation model shows that by increasing the length of the photochemical reactor and/or by increasing the photon intensity in said reactor, the feedstock utilization of [sup 196]Hg will be increased. Two preferred embodiments of the present invention are described, namely (1) long reactors using long photochemical lamps and vapor filters; and (2) quartz reactors with external UV reflecting films. These embodiments have each been constructed and operated, demonstrating the enhanced utilization process dictated by the mathematical model (also provided).

Grossman, M.W.; Mellor, C.E.

1993-04-27T23:59:59.000Z

128

Apparatus for control of mercury  

DOE Patents [OSTI]

A method and apparatus for reducing mercury in industrial gases such as the flue gas produced by the combustion of fossil fuels such as coal adds hydrogen sulfide to the flue gas in or just before a scrubber of the industrial process which contains the wet scrubber. The method and apparatus of the present invention is applicable to installations employing either wet or dry scrubber flue gas desulfurization systems. The present invention uses kraft green liquor as a source for hydrogen sulfide and/or the injection of mineral acids into the green liquor to release vaporous hydrogen sulfide in order to form mercury sulfide solids.

Downs, William (Alliance, OH); Bailey, Ralph T. (Uniontown, OH)

2001-01-01T23:59:59.000Z

129

Defining the Molecular-Cellular-Field Continuum of Mercury Detoxification  

SciTech Connect (OSTI)

Hg is of special interest to DOE due to past use at the Oak Ridge Reservation (ORR). Its facile redox [Hg2+/0] chemistry, bonding to carbon [e.g. MeHg+] and unique physical properties [e.g., Hg0 volatility] underlie a complex global Hg cycle involving biotic and abiotic chemical and physical transport and transformations in soils, sediments, waterways and the atmosphere. Facultative and anaerobic bacteria make MeHg+, which is neurotoxic to wildlife and humans. Sustainable stewardship requires eliminating both MeHg+ and even more toxic Hg2+, which is also the substrate for methylation. The proteins encoded by the mer locus in aerobic and facultative mercury resistant (HgR) bacteria convert soil or waterborne Hg2+ or MeHg+ to less toxic, gaseous Hg0. HgR microbes live in highly Hg-contaminated sites and depress MeHg+ formation >500-fold in such zones. So, enhancing the capacity of natural HgR microbes to remove Hg2+/MeHg+ from wetlands and waterways is a logical component of contaminated site stewardship. To apply enhancement in the field requires knowing how the HgR pathway works including the metabolic demands it makes on the cell, i.e., the entire cell is the relevant catalytic unit. HgR loci occur in metabolically diverse bacteria and unique mer-host co-evolution has been found. In this project we extended our previous studies of mer enzymes in ?-proteobacteria, which are abundant in high Hg areas of the ORR to include studies of mer enzymes from HgR ?-proteobacteria and HgR actinobacteria, which also increase in the high Hg regions of the ORR. Specifically, we (1) examined interactions between structural compoenents of MerA and MerB enzymes from ?-proteobacteria, (2) investigated effects of mutations on kinetic efficiency of Hg2+ reduction by ?-proteobacterial MerA, (3) cloned and performed initital characterization of MerA and MerB enzymes from Streptomyces lividans, an actinobacterium, (4) cloned and performed initial characterization of a fused MerB-MerA protein from Ochrobactrum anthropi, an ?-proteobacterium, (5) investigate the extent of Hg isotope fractionation that occurs with purified ?-proteobacterial MerA.

Miller, Susan M. [UCSF

2014-09-04T23:59:59.000Z

130

Molecular Mechanisms of Bacterial Mercury Transformation  

SciTech Connect (OSTI)

Mercury (Hg) is a major global pollutant arising from both natural and anthropogenic sources. Defining the factors that determine the relative affinities of different ligands for the mercuric ion, Hg2+, is critical to understanding its speciation, transformation, and bioaccumulation in the environment. Here, we used quantum chemistry to dissect the relative binding free energies for a series of inorganic anion complexes of Hg2+. The results show that, whereas in the gas phase the binding affinity of two identical anionic ligands (forming HgL2) increases with ligand (L) hardness, in contrast, in the aqueous phase the affinity increases with ligand softness. This switch in affinity upon hydration is shown to result mostly from interactions with only a small number (e.g. one or two) of water molecules. The results yield a clear, robust periodic trend within the chalcogenide and halide groups and are in agreement with the well-known experimentally observed preference of Hg2+ for soft ligands. By comparing the Hg2+ binding of one with two anions, the gas phase preferences are found to arise from the enhancement of reactivity of the cationic complex (HgL+) with the hardness of L. The approach establishes a theoretical basis for understanding Hg speciation in the biosphere.

smith, jeremy

2014-04-15T23:59:59.000Z

131

Blockage of IL-6 secretion in glia by lead and mercury  

E-Print Network [OSTI]

Mercury (Hg) and lead (Pb) are toxic to the development and function of the central nervous system (CNS). Interleukin-6 (IL 6) produced by astroglia protects neurons from damage in many progressive degenerative disorders. IL-6 secretion...

Pourrajabi, Nima Matthew

2003-01-01T23:59:59.000Z

132

Obtaining accurate amounts of mercury from mercury compounds via electrolytic methods  

DOE Patents [OSTI]

A process for obtaining pre-determined, accurate rate amounts of mercury. In one embodiment, predetermined, precise amounts of Hg are separated from HgO and plated onto a cathode wire. The method for doing this involves dissolving a precise amount of HgO which corresponds to a pre-determined amount of Hg desired in an electrolyte solution comprised of glacial acetic acid and H.sub.2 O. The mercuric ions are then electrolytically reduced and plated onto a cathode producing the required pre-determined quantity of Hg. In another embodiment, pre-determined, precise amounts of Hg are obtained from Hg.sub.2 Cl.sub.2. The method for doing this involves dissolving a precise amount of Hg.sub.2 Cl.sub.2 in an electrolyte solution comprised of concentrated HCl and H.sub.2 O. The mercurous ions in solution are then electrolytically reduced and plated onto a cathode wire producing the required, pre-determined quantity of Hg.

Grossman, Mark W. (Belmont, MA); George, William A. (Rockport, MA)

1987-01-01T23:59:59.000Z

133

Obtaining accurate amounts of mercury from mercury compounds via electrolytic methods  

DOE Patents [OSTI]

A process is described for obtaining pre-determined, accurate rate amounts of mercury. In one embodiment, predetermined, precise amounts of Hg are separated from HgO and plated onto a cathode wire. The method for doing this involves dissolving a precise amount of HgO which corresponds to a pre-determined amount of Hg desired in an electrolyte solution comprised of glacial acetic acid and H[sub 2]O. The mercuric ions are then electrolytically reduced and plated onto a cathode producing the required pre-determined quantity of Hg. In another embodiment, pre-determined, precise amounts of Hg are obtained from Hg[sub 2]Cl[sub 2]. The method for doing this involves dissolving a precise amount of Hg[sub 2]Cl[sub 2] in an electrolyte solution comprised of concentrated HCl and H[sub 2]O. The mercurous ions in solution are then electrolytically reduced and plated onto a cathode wire producing the required, pre-determined quantity of Hg. 1 fig.

Grossman, M.W.; George, W.A.

1987-07-07T23:59:59.000Z

134

Mercury Thermometer Replacement Alternatives Thermometer Description Non-Mercury Non-Mercury Non-Mercury  

E-Print Network [OSTI]

Mercury Thermometer Replacement Alternatives Length Thermometer Description Non-Mercury Non-Mercury Non-Mercury Range / Division VWR-Enviro-Safe® Fisherbrand® Brooklyn Thermometer Company Inc. Total/A #12;Mercury Thermometer Replacement Alternatives Length Thermometer Description Non-Mercury Non

135

Mercury extraction by the TRUEX process solvent: I. Kinetics, extractable species, dependence on nitric acid concentration and stoichiometry  

SciTech Connect (OSTI)

Mercury extraction from acidic aqueous solutions by the TRUEX process solvent (0.2 M CMPO, 1.4 M TBP in n-dodecane) has not extensively been examined. Research at the Idaho Chemical Processing Plant is currently in progress to evaluate the TRUEX process for actinide removal from several acidic waste streams, including liquid sodium-bearing waste (SBW), which contains significant quantities of mercury. Preliminary experiments were performed involving the extraction of Hg{sup 203}, added as HgCl{sub 2}, from 0.01 to 10 M HNO{sub 3} solutions. Mercury distribution coefficients (D{sub Hg}) range between 3 and 60 from 0.01 M to 2 M HNO{sub 3}. At higher nitric acid concentrations, i.e. 5 M HNO{sub 3} or greater, D{sub Hg} significantly decreases to values less than 1. These results indicate mercury is extracted from acidic solutions {<=}{approximately}2 M HNO{sub 3} and stripped with nitric acid solutions {>=}{approximately}5 M HNO{sub 3}. Experimental results indicate the extractable species is HgCl{sub 2} from nitrate media, i.e., chloride must be present in the nitrate feed to extract mercury. Extractions from Hg(NO{sub 3}){sub 2} solutions indicated substantially reduced distribution ratios, typically D{sub Hg}< 1, for the range of nitric acid concentrations examined (0.01 to 8 M HNO{sub 3}). Extraction of mercury, as HgCl{sub 2}, by the individual components of the TRUEX solvent was also examined from 2 M HNO{sub 3}. The diluent, n-dodecane, does not measurably extract mercury. With a 1.4 M TBP/n-dodecane solvent, D{sub Hg} {approximately}3.4 compared with D{sub Hg} {approximately}7 for the TRUEX solvent. Classical slope analysis techniques were utilized to evaluate the stoichiometric coefficients of Hg extraction independently for both CMPO and TBP.

Herbst, R.S.; Brewer, K.N.; Tranter, T.J.; Todd, T.A.

1995-12-01T23:59:59.000Z

136

6035 Hg(Ar) Lamp in 6058 Fiber Optic Accessory. Pencil Style Calibration Lamps  

E-Print Network [OSTI]

to that of the Hg(Ar) Lamp, which is the characteristic mercury line spectrum. Forced air-cooling (i.e. from of the handle for connection to the power supply. Table 1 Usable Wavelengths of Spectral Calibration Lamps (in.2 1079.8 1084.5 1114.3 Power Supplies; AC versus DC We offer different power supplies for different needs

Woodall, Jerry M.

137

A Stable Mercury-Containing Complex of the Organomercurial Lyase MerB: Catalysis, Product Release, and Direct Transfer to MerA  

E-Print Network [OSTI]

also be produced from less toxic forms of mercury by bacteria in aquatic sediments (4, 5). MeHg can mercury pollution (7). A variety of methods for the remediation of mercury pollution are proposed or in use (8). Some methods involve physical removal or decontamination of soil or water. An alternative

Scott, Robert A.

138

Assessment of atmospheric mercury emission reduction measures relevant for application in Poland  

SciTech Connect (OSTI)

Fuel combustion for heat and power generation, together with cement production, were the most significant sources of anthropogenic atmospheric mercury emission in Poland in 2003, with 57 and 27% of Hg emission, respectively. It was found that in Poland, Hg emission reduction measures need to be focused on the energy generation sector. Sorbent injection upstream of an electrostatic precipitator or fabric filter, mercury oxidation upstream of a wet or dry flue gas desulphurisation installation, together with Hg capture on sorbents, should be considered as priority in Polish conditions. This refers mainly to fuel combustion processes but also to the production of cement. For economic reasons it seems advisable that, apart from activated carbons as sorbents, application of zeolites obtained from power plant fly ash should also be considered. Application of primary methods seems to be very promising in Polish conditions, although they should be considered rather as an additional option apart from sorbent injection as the best option. Switching from coal to liquid and gaseous fuels shows the highest potential for reducing Hg emission. For chlorine production using the mercury cell electrolysis method, strict monitoring of Hg emissions and good housekeeping of Hg releasing processes seems a promising approach, but the main activity should focus on changing mercury-based technologies into membrane cell methods. Emission abatement potential for the atmospheric mercury in Poland has been roughly assessed, showing that in perspective of 2015, the emission could be reduced to about 25% of the anthropogenic atmospheric Hg emission in 2003.

Hlawiczka, S.; Fudala, J. [Institute for Ecology of Industrial Areas, Katowice (Poland)

2008-03-15T23:59:59.000Z

139

A study of the solubility of mercury in liquid hydrocarbons  

E-Print Network [OSTI]

mercury by precipitating HgS out of solution and measuring the metcury activity on a Gieger counter. A second but similar method used by Moser and Voigt used metallic Hg&cs which was obtained by reduction of mercumus nitrate with hypophosphorus acid...A STUDY OF THE SOLUBILITY OF MERCURY IN LIQUID HYDROCARBONS A Thesis by DAVID LARIhKR MCFARLANE Submitted to the Oflice of Graduate Studies of Texas A&M University in partial fulfillment of the requirements for the degree of MASTER...

McFarlane, David Larimer

1991-01-01T23:59:59.000Z

140

Modification of boiler operating conditions for mercury emissions reductions in coal-fired utility boilers  

E-Print Network [OSTI]

matter and char, and cold-end air pollution control devices. There is also evidence that boiler is equipped with hot and cold precipitators and a tubular air preheater. A strategy for mercury control designated hazardous air pollutants by the US Environmental Protection Agency (EPA), mercury (Hg) has

Li, Ying

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


141

Multiscale models of atmospheric mercury: bromine chemistry, air-sea exchange, and global transport  

E-Print Network [OSTI]

entrainment of RGM-rich air from the free troposphere (25­40%). Oxidation of Hg0 by Cl is minor (3Multiscale models of atmospheric mercury: bromine chemistry, air-sea exchange, and global transport Multiscale models of atmospheric mercury: bromine chemistry, air-sea exchange, and global transport Abstract

Holmes, Christopher D.

142

BEHAVIOR OF MERCURY DURING DWPF CHEMICAL PROCESS CELL PROCESSING  

SciTech Connect (OSTI)

The Defense Waste Processing Facility has experienced significant issues with the stripping and recovery of mercury in the Chemical Processing Cell (CPC). The stripping rate has been inconsistent, often resulting in extended processing times to remove mercury to the required endpoint concentration. The recovery of mercury in the Mercury Water Wash Tank has never been high, and has decreased significantly since the Mercury Water Wash Tank was replaced after the seventh batch of Sludge Batch 5. Since this time, essentially no recovery of mercury has been seen. Pertinent literature was reviewed, previous lab-scale data on mercury stripping and recovery was examined, and new lab-scale CPC Sludge Receipt and Adjustment Tank (SRAT) runs were conducted. For previous lab-scale data, many of the runs with sufficient mercury recovery data were examined to determine what factors affect the stripping and recovery of mercury and to improve closure of the mercury material balance. Ten new lab-scale SRAT runs (HG runs) were performed to examine the effects of acid stoichiometry, sludge solids concentration, antifoam concentration, form of mercury added to simulant, presence of a SRAT heel, operation of the SRAT condenser at higher than prototypic temperature, varying noble metals from none to very high concentrations, and higher agitation rate. Data from simulant runs from SB6, SB7a, glycolic/formic, and the HG tests showed that a significant amount of Hg metal was found on the vessel bottom at the end of tests. Material balance closure improved from 12-71% to 48-93% when this segregated Hg was considered. The amount of Hg segregated as elemental Hg on the vessel bottom was 4-77% of the amount added. The highest recovery of mercury in the offgas system generally correlated with the highest retention of Hg in the slurry. Low retention in the slurry (high segregation on the vessel bottom) resulted in low recovery in the offgas system. High agitation rates appear to result in lower retention of mercury in the slurry. Both recovery of mercury in the offgas system and removal (segregation + recovery) from the slurry correlate with slurry consistency. Higher slurry consistency results in better retention of Hg in the slurry (less segregation) and better recovery in the offgas system, but the relationships of recovery and retention with consistency are sludge dependent. Some correlation with slurry yield stress and acid stoichiometry was also found. Better retention of mercury in the slurry results in better recovery in the offgas system because the mercury in the slurry is stripped more easily than the segregated mercury at the bottom of the vessel. Although better retention gives better recovery, the time to reach a particular slurry mercury content (wt%) is longer than if the retention is poorer because the segregation is faster. The segregation of mercury is generally a faster process than stripping. The stripping factor (mass of water evaporated per mass of mercury stripped) of mercury at the start of boiling were found to be less than 1000 compared to the assumed design basis value of 750 (the theoretical factor is 250). However, within two hours, this value increased to at least 2000 lb water per lb Hg. For runs with higher mercury recovery in the offgas system, the stripping factor remained around 2000, but runs with low recovery had stripping factors of 4000 to 40,000. DWPF data shows similar trends with the stripping factor value increasing during boiling. These high values correspond to high segregation and low retention of mercury in the sludge. The stripping factor for a pure Hg metal bead in water was found to be about 10,000 lb/lb. About 10-36% of the total Hg evaporated in a SRAT cycle was refluxed back to the SRAT during formic acid addition and boiling. Mercury is dissolved as a result of nitric acid formation from absorption of NO{sub x}. The actual solubility of dissolved mercury in the acidic condensate is about 100 times higher than the actual concentrations measured. Mercury metal present in the MWWT from previous batch

Zamecnik, J.; Koopman, D.

2012-04-09T23:59:59.000Z

143

Manifold and method of batch measurement of Hg-196 concentration using a mass spectrometer  

DOE Patents [OSTI]

A sample manifold and method of its use has been developed so that milligram quantities of mercury can be analyzed mass spectroscopically to determine the .sup.196 Hg concentration to less than 0.02 atomic percent. Using natural mercury as a standard, accuracy of .+-.0.002 atomic percent can be obtained. The mass spectrometer preferably used is a commercially available GC/MS manufactured by Hewlett Packard. A novel sample manifold is contained within an oven allowing flow rate control of Hg into the MS. Another part of the manifold connects to an auxiliary pumping system which facilitates rapid clean up of residual Hg in the manifold. Sample cycle time is about 1 hour.

Grossman, Mark W. (Belmont, MA); Evans, Roger (N. Hampton, NH)

1991-01-01T23:59:59.000Z

144

Manifold and method of batch measurement of Hg-196 concentration using a mass spectrometer  

DOE Patents [OSTI]

A sample manifold and method of its use has been developed so that milligram quantities of mercury can be analyzed mass spectroscopically to determine the [sup 196]Hg concentration to less than 0.02 atomic percent. Using natural mercury as a standard, accuracy of [+-]0.002 atomic percent can be obtained. The mass spectrometer preferably used is a commercially available GC/MS manufactured by Hewlett Packard. A novel sample manifold is contained within an oven allowing flow rate control of Hg into the MS. Another part of the manifold connects to an auxiliary pumping system which facilitates rapid clean up of residual Hg in the manifold. Sample cycle time is about 1 hour. 8 figures.

Grossman, M.W.; Evans, R.

1991-11-26T23:59:59.000Z

145

Category:Mercury Vapor | Open Energy Information  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 NoPublic Utilities Address: 160Benin: EnergyBostonFacilityCascadeJump to:Lists Jump to: Jump to: navigation, search

146

Wide Range of Mercury Contamination in Chicks of Southern Ocean Seabirds  

E-Print Network [OSTI]

1 Wide Range of Mercury Contamination in Chicks of Southern Ocean Seabirds Pierre Blévina,* , Alice environment, Hg contamination was investigated within the large subantarctic seabird community of Kerguelen presented a wide range of Hg concentrations, with the highest contaminated species containing ~102 times

Boyer, Edmond

147

An Improved Global Model for Air-Sea Exchange of Mercury: High  

E-Print Network [OSTI]

An Improved Global Model for Air-Sea Exchange of Mercury: High Concentrations over the North by inputs from Hg enriched subsurface waters through entrainment and Ekman pumping. Globally, subsurface). Previous efforts to model Hg air-sea exchange (2) and atmospheric transport (4-6) have been unable

Holmes, Christopher D.

148

Mercury speciation driven by seasonal changes in a contaminated estuarine environment  

SciTech Connect (OSTI)

In this study, seasonal changes of mercury (Hg) species in the highly variable estuary of So?a/Isonzo River (northern Adriatic Sea) were investigated. Samplings were performed on a seasonal basis (September 2009, May, August and October 2010) and Hg species (total Hg, methylmercury (MeHg), dissolved gaseous Hg (DGM)) in waters, sediments and pore waters were determined. In addition, a range of ancillary parameters were measured (salinity, nutrients, organic carbon (OC), nitrogen species). Hg values were interpreted using these parameters and hydrological conditions (river flow, wave height) around the time of sampling. There were no significant changes in Hg load from river to the gulf, compared to previous studies. The load was temporarily higher in May 2010 due to higher river flow. Wave height, through changing hydrostatic pressure, was most likely to cause resuspension of already deposited Hg from the bottom (August 2010). The estuary is a net source of DGM to the atmosphere as suggested by DGM profiles, with salinity, redox potential and organic matter as the most probable controls over its production. MeHg is produced in situ in sediment or in water column, rather than transported by river, as indicated by its correlation with OC of the marine origin. Calculated fluxes for THg and MeHg showed sediment as a source for both the water column. In pore waters, OC in part affects partitioning of both THg and MeHg; however other factors (e.g. sulphide and/or oxyhydroxides precipitation and dissolution) are also probably important. -- Highlights: ? Water, sediment and pore water mercury species in front of So?a River estuary were measured. ? Seasonally variable hydrological conditions were shown to influence water column Hg speciation. ? Fluxes for total Hg and MeHg from sediment to water were calculated. ? Sediment is a source of total Hg and MeHg to the water column. ? Correlation of MeHg with organic carbon of marine origin suggests in situ formation.

Bratki?, Arne, E-mail: arne.bratkic@ijs.si [Department of Environmental Sciences, Joef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)] [Department of Environmental Sciences, Joef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia); Ogrinc, Nives, E-mail: nives.orginc@ijs.si [Department of Environmental Sciences, Joef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)] [Department of Environmental Sciences, Joef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia); Kotnik, Joe, E-mail: joze.kotnik@ijs.si [Department of Environmental Sciences, Joef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)] [Department of Environmental Sciences, Joef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia); Faganeli, Jadran, E-mail: faganeli@mbss.org [Marine Biology Station, Forna?e 41, 6330 Piran (Slovenia)] [Marine Biology Station, Forna?e 41, 6330 Piran (Slovenia); agar, Duan, E-mail: dusan.zagar@fgg.uni-lj.si [Faculty of Civil and Geodetic Engineering, Jamova 2, 1000 Ljubljana (Slovenia)] [Faculty of Civil and Geodetic Engineering, Jamova 2, 1000 Ljubljana (Slovenia); Yano, Shinichiro [Faculty of Engineering, Kyushu University, Fukuoka 812-8581 (Japan)] [Faculty of Engineering, Kyushu University, Fukuoka 812-8581 (Japan); Tada, Akihide, E-mail: tada@civil.nagasaki-u.ac.jp [Faculty of Engineering, Nagasaki University, Bunkyo-machi 1-14, Nagasaki 852-8521 (Japan)] [Faculty of Engineering, Nagasaki University, Bunkyo-machi 1-14, Nagasaki 852-8521 (Japan); Horvat, Milena, E-mail: milena.horvat@ijs.si [Department of Environmental Sciences, Joef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)] [Department of Environmental Sciences, Joef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)

2013-08-15T23:59:59.000Z

149

Exploring the structural basis for selenium/mercury antagonism in Allium fistulosum  

SciTech Connect (OSTI)

While continuing efforts are devoted to studying the mutually protective effect of mercury and selenium in mammals, few studies have investigated the mercury-selenium antagonism in plants. In this study, we report the metabolic fate of mercury and selenium in Allium fistulosum (green onion) after supplementation with sodium selenite and mercuric chloride. Analysis of homogenized root extracts via capillary reversed phase chromatography coupled with inductively coupled plasma mass spectrometry (capRPLC-ICP-MS) suggests the formation of a mercury-selenium containing compound. Micro-focused synchrotron X-ray fluorescence mapping of freshly excised roots show Hg sequestered on the root surface and outlining individual root cells, while Se is more evenly distributed throughout the root. There are also discrete Hg-only, Se-only regions and an overall strong correlation between Hg and Se throughout the root. Analysis of the X-ray absorption near edge structure (XANES) spectra show a 'background' of methylselenocysteine within the root with discrete spots of SeO{sub 3}{sup 2-}, Se{sup 0} and solid HgSe on the root surface. Mercury outlining individual root cells is possibly binding to sulfhydryl groups or plasma membrane or cell wall proteins, and in some places reacting with reduced selenium in the rhizosphere to form a mercury(II) selenide species. Together with the formation of the root-bound mercury(II) selenide species, we also report on the formation of cinnabar (HgS) and Hg{sup 0} in the rhizosphere. The results presented herein shed light on the intricate chemical and biological processes occurring within the rhizosphere that influence Hg and Se bioavailability and will be instrumental in predicting the fate and assisting in the remediation of these metals in the environment and informing whether or not fruit and vegetable food selection from aerial plant compartments or roots from plants grown in Hg contaminated soils, are safe for consumption.

McNear, Jr., David H.; Afton, Scott E.; Caruso, Joseph A. (UCIN); (Kentucky)

2012-12-10T23:59:59.000Z

150

Mercury Continuous Emmission Monitor Calibration  

SciTech Connect (OSTI)

Mercury continuous emissions monitoring systems (CEMs) are being implemented in over 800 coal-fired power plant stacks throughput the U.S. Western Research Institute (WRI) is working closely with the Electric Power Research Institute (EPRI), the National Institute of Standards and Technology (NIST), and the Environmental Protection Agency (EPA) to facilitate the development of the experimental criteria for a NIST traceability protocol for dynamic elemental mercury vapor calibrators/generators. These devices are used to calibrate mercury CEMs at power plant sites. The Clean Air Mercury Rule (CAMR) which was published in the Federal Register on May 18, 2005 and vacated by a Federal appeals court in early 2008 required that calibration be performed with NIST-traceable standards. Despite the vacature, mercury emissions regulations in the future will require NIST traceable calibration standards, and EPA does not want to interrupt the effort towards developing NIST traceability protocols. The traceability procedures will be defined by EPA. An initial draft traceability protocol was issued by EPA in May 2007 for comment. In August 2007, EPA issued a conceptual interim traceability protocol for elemental mercury calibrators. The protocol is based on the actual analysis of the output of each calibration unit at several concentration levels ranging initially from about 2-40 {micro}g/m{sup 3} elemental mercury, and in the future down to 0.2 {micro}g/m{sup 3}, and this analysis will be directly traceable to analyses by NIST. The EPA traceability protocol document is divided into two separate sections. The first deals with the qualification of calibrator models by the vendors for use in mercury CEM calibration. The second describes the procedure that the vendors must use to certify the calibrators that meet the qualification specifications. The NIST traceable certification is performance based, traceable to analysis using isotope dilution inductively coupled plasma/mass spectrometry (ID/ICP/MS) performed by NIST in Gaithersburg, MD. The outputs of mercury calibrators are compared to one another using a nesting procedure which allows direct comparison of one calibrator with another at specific concentrations and eliminates analyzer variability effects. The qualification portion of the EPA interim traceability protocol requires the vendors to define calibrator performance as affected by variables such as pressure, temperature, line voltage, and shipping. In 2007 WRI developed and conducted a series of simplified qualification experiments to determine actual calibrator performance related to the variables defined in the qualification portion of the interim protocol.

John Schabron; Eric Kalberer; Ryan Boysen; William Schuster; Joseph Rovani

2009-03-12T23:59:59.000Z

151

Mixed Waste Focus Area mercury contamination product line: An integrated approach to mercury waste treatment and disposal  

SciTech Connect (OSTI)

The US Department of Energy (DOE) Mixed Waste Focus Area (MWFA) is tasked with ensuring that solutions are available for the mixed waste treatment problems of the DOE complex. During the MWFA`s initial technical baseline development process, three of the top four technology deficiencies identified were related to the need for amalgamation, stabilization, and separation/removal technologies for the treatment of mercury and mercury-contaminated mixed waste. The focus area grouped mercury-waste-treatment activities into the mercury contamination product line under which development, demonstration, and deployment efforts are coordinated to provide tested technologies to meet the site needs. The Mercury Working Group (HgWG), a selected group of representatives from DOE sites with significant mercury waste inventories, is assisting the MWFA in soliciting, identifying, initiating, and managing efforts to address these areas. Based on the scope and magnitude of the mercury mixed waste problem, as defined by HgWG, solicitations and contract awards have been made to the private sector to demonstrate amalgamation and stabilization processes using actual mixed wastes. Development efforts are currently being funded under the product line that will address DOE`s needs for separation/removal processes. This paper discusses the technology selection process, development activities, and the accomplishments of the MWFA to date through these various activities.

Hulet, G.A. [Lockheed Martin Idaho Technologies Co., Idaho Falls, ID (United States); Conley, T.B.; Morris, M.I. [Oak Ridge National Lab., TN (United States)

1998-07-01T23:59:59.000Z

152

Analysis of Halogen-Mercury Reactions in Flue Gas  

SciTech Connect (OSTI)

Oxidized mercury species may be formed in combustion systems through gas-phase reactions between elemental mercury and halogens, such as chorine or bromine. This study examines how bromine species affect mercury oxidation in the gas phase and examines the effects of mixtures of bromine and chlorine on extents of oxidation. Experiments were conducted in a bench-scale, laminar flow, methane-fired (300 W), quartz-lined reactor in which gas composition (HCl, HBr, NO{sub x}, SO{sub 2}) and temperature profile were varied. In the experiments, the post-combustion gases were quenched from flame temperatures to about 350 C, and then speciated mercury was measured using a wet conditioning system and continuous emissions monitor (CEM). Supporting kinetic calculations were performed and compared with measured levels of oxidation. A significant portion of this report is devoted to sample conditioning as part of the mercury analysis system. In combustion systems with significant amounts of Br{sub 2} in the flue gas, the impinger solutions used to speciate mercury may be biased and care must be taken in interpreting mercury oxidation results. The stannous chloride solution used in the CEM conditioning system to convert all mercury to total mercury did not provide complete conversion of oxidized mercury to elemental, when bromine was added to the combustion system, resulting in a low bias for the total mercury measurement. The use of a hydroxylamine hydrochloride and sodium hydroxide solution instead of stannous chloride showed a significant improvement in the measurement of total mercury. Bromine was shown to be much more effective in the post-flame, homogeneous oxidation of mercury than chlorine, on an equivalent molar basis. Addition of NO to the flame (up to 400 ppmv) had no impact on mercury oxidation by chlorine or bromine. Addition of SO{sub 2} had no effect on mercury oxidation by chlorine at SO{sub 2} concentrations below about 400 ppmv; some increase in mercury oxidation was observed at SO{sub 2} concentrations of 400 ppmv and higher. In contrast, SO{sub 2} concentrations as low as 50 ppmv significantly reduced mercury oxidation by bromine, this reduction could be due to both gas and liquid phase interactions between SO{sub 2} and oxidized mercury species. The simultaneous presence of chlorine and bromine in the flue gas resulted in a slight increase in mercury oxidation above that obtained with bromine alone, the extent of the observed increase is proportional to the chlorine concentration. The results of this study can be used to understand the relative importance of gas-phase mercury oxidation by bromine and chlorine in combustion systems. Two temperature profiles were tested: a low quench (210 K/s) and a high quench (440 K/s). For chlorine the effects of quench rate were slight and hard to characterize with confidence. Oxidation with bromine proved sensitive to quench rate with significantly more oxidation at the lower rate. The data generated in this program are the first homogeneous laboratory-scale data on bromine-induced oxidation of mercury in a combustion system. Five Hg-Cl and three Hg-Br mechanisms, some published and others under development, were evaluated and compared to the new data. The Hg-halogen mechanisms were combined with submechanisms from Reaction Engineering International for NO{sub x}, SO{sub x}, and hydrocarbons. The homogeneous kinetics under-predicted the levels of mercury oxidation observed in full-scale systems. This shortcoming can be corrected by including heterogeneous kinetics in the model calculations.

Paula Buitrago; Geoffrey Silcox; Constance Senior; Brydger Van Otten

2010-01-01T23:59:59.000Z

153

DATABASE Open Access Regional distribution of mercury in sediments  

E-Print Network [OSTI]

DATABASE Open Access Regional distribution of mercury in sediments of the main rivers of French led to locally high concentrations in soils and sediments. The present study maps the levels of Hg concentrations in river sediments from five main rivers of French Guiana (Approuague River, Comté River, Mana

Boyer, Edmond

154

Dark Oxidation of Dissolved and Liquid Elemental Mercury in Aquatic  

E-Print Network [OSTI]

Sherbrooke Street West, Montreal, Quebec H3A 2K6, Canada Elemental mercury (Hg0) can be found in liquid that this oxidation is greatly enhanced by solar radiation, par- ticularly-sterilized, treated with chloroform, or filtered prior to exposure to light. Laboratory experiments have also shown

Morel, Franois M. M.

155

Selective partitioning of mercury from co-extracted actinides in a simulated acidic ICPP waste stream  

SciTech Connect (OSTI)

The TRUEX process is being evaluated at the Idaho Chemical Processing Plant (ICPP) as a means to partition the actinides from acidic sodium-bearing waste (SBW). The mercury content of this waste averages 1 g/l. Because the chemistry of mercury has not been extensively evaluated in the TRUEX process, mercury was singled out as an element of interest. Radioactive mercury, {sup 203}Hg, was spiked into a simulated solution of SBW containing 1 g/l mercury. Successive extraction batch contacts with the mercury spiked waste simulant and successive scrubbing and stripping batch contacts of the mercury loaded TRUEX solvent (0.2 M CMPO-1.4 M TBP in dodecane) show that mercury will extract into and strip from the solvent. The extraction distribution coefficient for mercury, as HgCl{sub 2} from SBW having a nitric acid concentration of 1.4 M and a chloride concentration of 0.035 M was found to be 3. The stripping distribution coefficient was found to be 0.5 with 5 M HNO{sub 3} and 0.077 with 0.25 M Na{sub 2}CO{sub 3}. An experimental flowsheet was designed from the batch contact tests and tested counter-currently using 5.5 cm centrifugal contactors. Results from the counter-current test show that mercury can be removed from the acidic mixed SBW simulant and recovered separately from the actinides.

Brewer, K.N.; Herbst, R.S.; Tranter, T.J. [and others

1995-12-01T23:59:59.000Z

156

Glutathione enzyme and selenoprotein polymorphisms associate with mercury biomarker levels in Michigan dental professionals  

SciTech Connect (OSTI)

Mercury is a potent toxicant of concern to both the general public and occupationally exposed workers (e.g., dentists). Recent studies suggest that several genes mediating the toxicokinetics of mercury are polymorphic in humans and may influence inter-individual variability in mercury accumulation. This work hypothesizes that polymorphisms in key glutathione synthesizing enzyme, glutathione s-transferase, and selenoprotein genes underlie inter-individual differences in mercury body burden as assessed by analytical mercury measurement in urine and hair, biomarkers of elemental mercury and methylmercury, respectively. Urine and hair samples were collected from a population of dental professionals (n = 515), and total mercury content was measured. Average urine (1.06 {+-} 1.24 ug/L) and hair mercury levels (0.49 {+-} 0.63 ug/g) were similar to national U.S. population averages. Taqman assays were used to genotype DNA from buccal swab samples at 15 polymorphic sites in genes implicated in mercury metabolism. Linear regression modeling assessed the ability of polymorphisms to modify the relationship between mercury biomarker levels and exposure sources (e.g., amalgams, fish consumption). Five polymorphisms were significantly associated with urine mercury levels (GSTT1 deletion), hair mercury levels (GSTP1-105, GSTP1-114, GSS 5 Prime ), or both (SEPP1 3 Prime UTR). Overall, this study suggests that polymorphisms in selenoproteins and glutathione-related genes may influence elimination of mercury in the urine and hair or mercury retention following exposures to elemental mercury (via dental amalgams) and methylmercury (via fish consumption). -- Highlights: Black-Right-Pointing-Pointer We explore the influence of 15 polymorphisms on urine and hair Hg levels. Black-Right-Pointing-Pointer Urine and hair Hg levels in dental professionals were similar to the US population. Black-Right-Pointing-Pointer GSTT1 and SEPP1 polymorphisms associated with urine Hg levels. Black-Right-Pointing-Pointer Accumulation of Hg in hair following exposure from fish was modified by genotype. Black-Right-Pointing-Pointer GSTP1, GSS, and SEPP1 polymorphisms influenced Hg accumulation in hair.

Goodrich, Jaclyn M.; Wang, Yi [Department of Environmental Health Sciences, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI 48109 (United States)] [Department of Environmental Health Sciences, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI 48109 (United States); Gillespie, Brenda [Department of Biostatistics, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI 48109 (United States)] [Department of Biostatistics, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI 48109 (United States); Werner, Robert [Department of Environmental Health Sciences, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI 48109 (United States) [Department of Environmental Health Sciences, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI 48109 (United States); Department of Physical Medicine and Rehabilitation, University of Michigan, 325 E. Eisenhower Parkway Suite 100, Ann Arbor, MI 48108 (United States); Franzblau, Alfred [Department of Environmental Health Sciences, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI 48109 (United States)] [Department of Environmental Health Sciences, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI 48109 (United States); Basu, Niladri, E-mail: niladri@umich.edu [Department of Environmental Health Sciences, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI 48109 (United States)] [Department of Environmental Health Sciences, University of Michigan School of Public Health, 1415 Washington Heights, Ann Arbor, MI 48109 (United States)

2011-12-15T23:59:59.000Z

157

Molecular structure and dynamics in bacterial mercury resistance  

SciTech Connect (OSTI)

Bacteria participate significantly in mercury transformation in natural and industrial environments. Previous studies have shown that bacterial mercury resistance is mediated by the mer operon, typically located on transposons or plasmids. It encodes specific genes that facilitate uptake of mercury species, cleavage of organomercurials, and reduction of Hg(II) to Hg(0). Expression of mer operon genes is regulated by MerR, a metal-responsive regulator protein on the level of transcription. In vitro studies have shown that MerR forms a non-transcribing pre-initiation complex with RNA polymerase and the promoter DNA. Binding of Hg(II) induces conformational changes in MerR and other components of the complex resulting in the transcription of mer operon genes. As part of ongoing investigations on allosteric conformational changes induced by Hg(II) in dimeric MerR, and the implications on the binding of RNA polymerase to the promoter of the mer operon, we applied small angle scattering to study the regulatory mechanism of MerR in the presence and absence of Hg(II). Our results show that in the presence of Hg(II) the MerR dimer undergoes a significant reorientation from a compact state to a conformation revealing two distinct domains. Bacterial reduction of Hg(II) can also occur at concentrations too low to induce mer operon functions. Dissimilatory metal reducing bacteria, such as Shewanella and Geobacter are able to reduce Hg(II) in the presence of mineral oxides. This process has been linked to the activity of outer membrane multiheme cytochromes. We isolated and purified a decaheme outer membrane cytochrome OmcA from Shewanella oneidensis MR-1 and characterized its envelope shape in solution by small angle x-ray scattering. Structural features were identified and compared to homology models. These results show that OmcA is an elongated macromolecule consisting of separate modules, which may be connected by flexible linkers.

Johs, Alexander [ORNL] [ORNL; Shi, Liang [ORNL] [ORNL; Miller, Susan M [ORNL] [ORNL; Summers, Anne O [ORNL] [ORNL; Liang, Liyuan [ORNL] [ORNL

2008-01-01T23:59:59.000Z

158

SULFUR POLYMER STABILIZATION/SOLIDIFICATION (SPSS) TREATABILITY OF LOS ALAMOS NATIONAL LABORATORY MERCURY WASTE.  

SciTech Connect (OSTI)

Brookhaven National Laboratory's Sulfur Polymer Stabilization/Solidification (SPSS) process was used to treat approximately 90kg of elemental mercury mixed waste from Los Alamos National Laboratory. Treatment was carried out in a series of eight batches using a 1 ft{sup 3} pilot-scale mixer, where mercury loading in each batch was 33.3 weight percent. Although leach performance is currently not regulated for amalgamated elemental mercury (Hg) mixed waste, Toxicity Characteristic Leach Procedure (TCLP) testing of SPSS treated elemental mercury waste indicates that leachability is readily reduced to below the TCLP limit of 200 ppb (regulatory requirement following treatment by retort for wastes containing > 260 ppb Hg), and with process optimization, to levels less than the stringent Universal Treatment Standard (UTS) limit of 25 ppb that is applied to waste containing < 260 ppm Hg. In addition, mercury-contaminated debris, consisting of primary glass and plastic containers, as well as assorted mercury thermometers, switches, and labware, was first reacted with SPSS components to stabilize the mercury contamination, then macroencapsulated in the molten SPSS product. This treatment was done by vigorous agitation of the sulfur polymer powder and the comminuted debris. Larger plastic and metal containers were reacted to stabilize internal mercury contamination, and then filled with molten sulfur polymer to encapsulate the treated product.

ADAMS,J.W.; KALB,P.D.

2001-11-01T23:59:59.000Z

159

Catalysts for oxidation of mercury in flue gas  

DOE Patents [OSTI]

Two new classes of catalysts for the removal of heavy metal contaminants, especially mercury (Hg) from effluent gases. Both of these classes of catalysts are excellent absorbers of HCl and Cl.sub.2 present in effluent gases. This adsorption of oxidizing agents aids in the oxidation of heavy metal contaminants. The catalysts remove mercury by oxidizing the Hg into mercury (II) moieties. For one class of catalysts, the active component is selected from the group consisting of iridium (Ir) and iridum-platinum (Ir/Pt) alloys. The Ir and Ir/Pt alloy catalysts are especially corrosion resistant. For the other class of catalyst, the active component is partially combusted coal or "Thief" carbon impregnated with Cl.sub.2. Untreated Thief carbon catalyst can be self-activating in the presence of effluent gas streams. The Thief carbon catalyst is disposable by means of capture from the effluent gas stream in a particulate collection device (PCD).

Granite, Evan J. (Wexford, PA); Pennline, Henry W. (Bethel Park, PA)

2010-08-17T23:59:59.000Z

160

DOI: 10.1002/chem.201103348 Mercury(II) Ion Detection via Pyrene-Mediated Photolysis of  

E-Print Network [OSTI]

of the environment with heavy metal ions has created a pressing public health concern in living sys- tems. Mercury pair.[12] In addition, Hg2+ shows an excellent selectivity against other heavy and transition-metal recognized accumulative and toxic characters in the envi- ronment and the ecosystem. The sources of mercury

Tan, Weihong

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161

Experiences in long-term evaluation of mercury emission monitoring systems  

SciTech Connect (OSTI)

Six mercury continuous emission monitoring (CEM) systems provided by two leading mercury (Hg) CEM system manufacturers were tested at five coal combustion utilities. The linearity, response time, day-to-day stability, efficiency of the Hg speciation modules, and ease of use were evaluated by following procedures specified in the Code of Federal Regulation Title 40 Part 75 (40 CFR Part 75). Mercury monitoring results from Hg CEM systems were compared to an EPA-recognized reference method. A sorbent trap sampling system was also evaluated in this study to compare the relative accuracy to the reference method as well as to Hg CEM systems. A conceptual protocol proposed by U.S. EPA (Method 30A) for using an Hg CEM system as the reference method for the Hg relative accuracy (RA) test was also followed to evaluate the workability of the protocol. This paper discusses the operational experience obtained from these field studies and the remaining challenges to overcome while using Hg CEM systems and the sorbent trap method for continuous Hg emission monitoring. 3 refs., 5 figs., 11 tabs.

Chin-Min Cheng; Hung-Ta Lin; Qiang Wang; Chien-Wei Chen; Chia-Wei Wang; Ming-Chung Liu; Chi-Kuan Chen; Wei-Ping Pan [Western Kentucky University, Bowling Green, KY (United States). Institute for Combustion Science and Environmental Technology

2008-09-15T23:59:59.000Z

162

Hg supply piping simulation Stony Brook University  

E-Print Network [OSTI]

Hg supply piping simulation (No MHD) Stony Brook University Yan Zhan Prof. Foluso Ladeinde July 2nd, 2010 #12;Outline · Hg supply piping in Muon Collider · Turbulence models for bend pipe flow · Problems need studying · Arrangements in the near future #12;Outline · Hg supply piping in Muon Collider ­ Hg

McDonald, Kirk

163

Hg Delivery System Vacuum 25 Oct 2005  

E-Print Network [OSTI]

. S. DEPARTMENT OF ENERGY V. Graves 25 Oct 2005 MERIT Mtg at MIT Oct 17-19 · During Hg delivery system to both design and operations #12;3 OAK RIDGE NATIONAL LABORATORY U. S. DEPARTMENT OF ENERGY V. Graves 25 & return lines - Sump tank & all connecting ports - Hg cylinder & bellows Hg inlet Hg cylinder & Bellows

McDonald, Kirk

164

Mercury contamination extraction  

DOE Patents [OSTI]

Mercury is removed from contaminated waste by firstly applying a sulfur reagent to the waste. Mercury in the waste is then permitted to migrate to the reagent and is stabilized in a mercury sulfide compound. The stable compound may then be removed from the waste which itself remains in situ following mercury removal therefrom.

Fuhrmann, Mark (Silver Spring, MD); Heiser, John (Bayport, NY); Kalb, Paul (Wading River, NY)

2009-09-15T23:59:59.000Z

165

Stimulation of erythrocyte phosphatidylserine exposure by mercury ions  

SciTech Connect (OSTI)

The sequelae of mercury intoxication include induction of apoptosis. In nucleated cells, Hg{sup 2+}-induced apoptosis involves mitochondrial damage. The present study has been performed to elucidate effects of Hg{sup 2+} in erythrocytes which lack mitochondria but are able to undergo apoptosis-like alterations of the cell membrane. Previous studies have documented that activation of a Ca{sup 2+}-sensitive erythrocyte scramblase leads to exposure of phosphatidylserine at the erythrocyte surface, a typical feature of apoptotic cells. The erythrocyte scramblase is activated by osmotic shock, oxidative stress and/or energy depletion which increase cytosolic Ca{sup 2+} activity and/or activate a sphingomyelinase leading to formation of ceramide. Ceramide sensitizes the scramblase to Ca{sup 2+}. The present experiments explored the effect of Hg{sup 2+} ions on erythrocytes. Phosphatidylserine exposure after mercury treatment was estimated from annexin binding as determined in FACS analysis. Exposure to Hg{sup 2+} (1 {mu}M) indeed significantly increased annexin binding from 2.3 {+-} 0.5% (control condition) to 23 {+-} 6% (n = 6). This effect was paralleled by activation of a clotrimazole-sensitive K{sup +}-selective conductance as measured by patch-clamp recordings and by transient cell shrinkage. Further experiments revealed also an increase of ceramide formation by {approx}66% (n = 7) after challenge with mercury (1 {mu}M). In conclusion, mercury ions activate a clotrimazole-sensitive K{sup +}-selective conductance leading to transient cell shrinkage. Moreover, Hg{sup 2+} increases ceramide formation. The observed mechanisms could similarly participate in the triggering of apoptosis in nucleated cells by Hg{sup 2+}.

Eisele, Kerstin [Department of Physiology, University of Tuebingen (Germany); Lang, Philipp A. [Department of Physiology, University of Tuebingen (Germany); Kempe, Daniela S. [Department of Physiology, University of Tuebingen (Germany); Klarl, Barbara A. [Department of Physiology, University of Tuebingen (Germany); Niemoeller, Olivier [Department of Physiology, University of Tuebingen (Germany); Wieder, Thomas [Department of Physiology, University of Tuebingen (Germany); Huber, Stephan M. [Department of Physiology, University of Tuebingen (Germany); Duranton, Christophe [Department of Physiology, University of Tuebingen (Germany); Lang, Florian [Department of Physiology, University of Tuebingen (Germany)]. E-mail: florian.lang@uni-tuebingen.de

2006-01-15T23:59:59.000Z

166

MERIT Hg System Design Update  

E-Print Network [OSTI]

tank · Multiple Hg cylinder ports #12;4 OAK RIDGE NATIONAL LABORATORY U. S. DEPARTMENT OF ENERGY MERIT Princeton University Nov 17-18, 2005 #12;2 OAK RIDGE NATIONAL LABORATORY U. S. DEPARTMENT OF ENERGY MERIT distortion #12;3 OAK RIDGE NATIONAL LABORATORY U. S. DEPARTMENT OF ENERGY MERIT Collab. Mtg Nov 17-18, 2005

McDonald, Kirk

167

Sulfur Impregnation on Activated Carbon Fibers through H2S Oxidation for Vapor Phase  

E-Print Network [OSTI]

Sulfur Impregnation on Activated Carbon Fibers through H2S Oxidation for Vapor Phase Mercury: Sulfur was impregnated onto activated carbon fibers ACFs through H2S oxidation catalyzed by the sorbent CE Database subject headings: Activated carbon; Sulfur; Mercury; Hydrogen sulfides; Oxidation

Borguet, Eric

168

Oxidation of Mercury in Products of Coal Combustion  

SciTech Connect (OSTI)

Laboratory measurements of mercury oxidation during selective catalytic reduction (SCR) of nitric oxide, simulation of pilot-scale measurements of mercury oxidation and adsorption by unburned carbon and fly ash, and synthesis of new materials for simultaneous oxidation and adsorption of mercury, were performed in support of the development of technology for control of mercury emissions from coal-fired boilers and furnaces. Conversion of gas-phase mercury from the elemental state to water-soluble oxidized form (HgCl{sub 2}) enables removal of mercury during wet flue gas desulfurization. The increase in mercury oxidation in a monolithic V{sub 2}O{sub 5}-WO{sub 3}/TiO{sub 2} SCR catalyst with increasing HCl at low levels of HCl (< 10 ppmv) and decrease in mercury oxidation with increasing NH{sub 3}/NO ratio during SCR were consistent with results of previous work by others. The most significant finding of the present work was the inhibition of mercury oxidation in the presence of CO during SCR of NO at low levels of HCl. In the presence of 2 ppmv HCl, expected in combustion products from some Powder River Basin coals, an increase in CO from 0 to 50 ppmv reduced the extent of mercury oxidation from 24 {+-} 3 to 1 {+-} 4%. Further increase in CO to 100 ppmv completely suppressed mercury oxidation. In the presence of 11-12 ppmv HCl, increasing CO from 0 to {approx}120 ppmv reduced mercury oxidation from {approx}70% to 50%. Conversion of SO{sub 2} to sulfate also decreased with increasing NH{sub 3}/NO ratio, but the effects of HCl and CO in flue gas on SO{sub 2} oxidation were unclear. Oxidation and adsorption of mercury by unburned carbon and fly ash enables mercury removal in a particulate control device. A chemical kinetic mechanism consisting of nine homogeneous and heterogeneous reactions for mercury oxidation and removal was developed to interpret pilot-scale measurements of mercury oxidation and adsorption by unburned carbon and fly ash in experiments at pilot scale, burning bituminous coals (Gale, 2006) and blends of bituminous coals with Powder River Basin coal (Gale, 2005). The removal of mercury by fly ash and unburned carbon in the flue gas from combustion of the bituminous coals and blends was reproduced with satisfactory accuracy by the model. The enhancement of mercury capture in the presence of calcium (Gale, 2005) explained a synergistic effect of blending on mercury removal across the baghouse. The extent of mercury oxidation, on the other hand, was not so well described by the simulation, because of oversensitivity of the oxidation process in the model to the concentration of unburned carbon. Combined catalysts and sorbents for oxidation and removal of mercury from flue gas at low temperature were based on surfactant-templated silicas containing a transition metal and an organic functional group. The presence of both metal ions and organic groups within the pore structure of the materials is expected to impart to them the ability to simultaneously oxidize elemental mercury and adsorb the resulting oxidized mercury. Twelve mesoporous organosilicate catalysts/sorbents were synthesized, with and without metals (manganese, titanium, vanadium) and organic functional groups (aminopropyl, chloropropyl, mercaptopropyl). Measurement of mercury oxidation and adsorption by the candidate materials remains for future work.

Peter Walsh; Giang Tong; Neeles Bhopatkar; Thomas Gale; George Blankenship; Conrad Ingram; Selasi Blavo Tesfamariam Mehreteab; Victor Banjoko; Yohannes Ghirmazion; Heng Ban; April Sibley

2009-09-14T23:59:59.000Z

169

Phytoremediation of Ionic and Methyl Mercury P  

SciTech Connect (OSTI)

Our long-term goal is to enable highly productive plant species to extract, resist, detoxify, and/or sequester toxic heavy metal pollutants as an environmentally friendly alternative to physical remediation methods. We have focused this phytoremediation research on soil and water-borne ionic and methylmercury. Mercury pollution is a serious world-wide problem affecting the health of human and wild-life populations. Methylmercury, produced by native bacteria at mercury-contaminated wetland sites, is a particularly serious problem due to its extreme toxicity and efficient biomagnification in the food chain. We engineered several plant species (e.g., Arabidopsis, tobacco, canola, yellow poplar, rice) to express the bacterial genes, merB and/or merA, under the control of plant regulatory sequences. These transgenic plants acquired remarkable properties for mercury remediation. (1) Transgenic plants expressing merB (organomercury lyase) extract methylmercury from their growth substrate and degrade it to less toxic ionic mercury. They grow on concentrations of methylmercury that kill normal plants and accumulate low levels of ionic mercury. (2) Transgenic plants expressing merA (mercuric ion reductase) extract and electrochemically reduce toxic, reactive ionic mercury to much less toxic and volatile metallic mercury. This metal transformation is driven by the powerful photosynthetic reducing capacity of higher plants that generates excess NADPH using solar energy. MerA plants grow vigorously on levels of ionic mercury that kill control plants. Plants expressing both merB and merA degrade high levels of methylmercury and volatilize metallic mercury. These properties were shown to be genetically stable for several generations in the two plant species examined. Our work demonstrates that native trees, shrubs, and grasses can be engineered to remediate the most abundant toxic mercury pollutants. Building on these data our working hypothesis for the next grant period is that transgenic plants expressing the bacterial merB and merA genes will (a) remove mercury from polluted soil and water and (b) prevent methylmercury from entering the food chain. Our specific aims center on understanding the mechanisms by which plants process the various forms of mercury and volatilize or transpire mercury vapor. This information will allow us to improve the design of our current phytoremediation strategies. As an alternative to volatilizing mercury, we are using several new genes to construct plants that will hyperaccumulate mercury in above-ground tissues for later harvest. The Department of Energy's Oak Ridge National Laboratory and Brookhaven National Laboratory have sites with significant levels of mercury contamination that could be cleaned by applying the scientific discoveries and new phytoremediation technologies described in this proposal. The knowledge and expertise gained by engineering plants to hyperaccumulate mercury can be applied to the remediation of other heavy metals pollutants (e.g., arsenic, cesium, cadmium, chromium, lead, strontium, technetium, uranium) found at several DOE facilities.

Meagher, Richard B.

1999-06-01T23:59:59.000Z

170

Mercury stabilization in chemically bonded phosphate ceramics  

SciTech Connect (OSTI)

Mercury stabilization and solidification is a significant challenge for conventional stabilization technologies. This is because of the stringent regulatory limits on leaching of its stabilized products. In a conventional cement stabilization process, Hg is converted at high pH to its hydroxide, which is not a very insoluble compound; hence the preferred route for Hg sulfidation to convert it into insoluble cinnabar (HgS). Unfortunately, efficient formation of this compound is pH-dependent. At a high pH, one obtains a more soluble Hg sulfate, in a very low pH range, insufficient immobilization occurs because of the escape of hydrogen sulfide, while efficient formation of HgS occurs only in a moderately acidic region. Thus, the pH range of 4 to 8 is where stabilization with Chemically Bonded Phosphate Ceramics (CBPC) is carried out. This paper discusses the authors experience on bench-scale stabilization of various US Department of Energy (DOE) waste streams containing Hg in the CBPC process. This process was developed to treat DOE's mixed waste streams. It is a room-temperature-setting process based on an acid-base reaction between magnesium oxide and monopotassium phosphate solution that forms a dense ceramic within hours. For Hg stabilization, addition of a small amount (< 1 wt.%) of Na{sub 2}S or K{sub 2}S is sufficient in the binder composition. Here the Toxicity Characteristic Leaching Procedure (TCLP) results on CBPC waste forms of surrogate waste streams representing secondary Hg containing wastes such as combustion residues and Delphi DETOX{trademark} residues are presented. The results show that although the current limit on leaching of Hg is 0.2 mg/L, the results from the CBPC waste forms are at least one order lower than this stringent limit. Encouraged by these results on surrogate wastes, they treated actual low-level Hg-containing mixed waste from their facility at Idaho. TCLP results on this waste are presented here. The efficient stabilization in all these cases is attributed to chemical immobilization as both a sulfide (cinnabar) and a phosphate, followed by its physical encapsulation in a dense matrix of the ceramic.

Wagh, A. S.; Singh, D.; Jeong, S. Y.

2000-04-04T23:59:59.000Z

171

Mercury reduction and cell-surface adsorption by Geobacter sulfurreducens PCA  

SciTech Connect (OSTI)

Both reduction and surface adsorption of mercuric mercury [Hg(II)] are found to occur simultaneously on G. sulfurreducens PCA cells under dark, anaerobic conditions. Reduction of Hg(II) to elemental Hg(0) initially follows a pseudo-first order kinetics with a half-life of < 2 h in the presence of 50 nM Hg(II) and 1011 cells L-1 in a phosphate buffer (pH 7.4). Multiple gene deletions of the outer membrane cytochromes in this organism resulted in decrease in reduction rate from ~ 0.3 to 0.05 h-1, and reduction was nearly absent with heat-killed cells or in the cell filtrate. Adsorption of Hg(II) by cells is found to compete with, and thus inhibit, Hg(II) reduction. Depending on the Hg to cell ratio, maximum Hg(II) reduction was observed at about 5 10-19 mol Hg cell-1, but reduction terminated at a low Hg to cell ratio (< 10-20 mol Hg cell-1). This inhibitory effect is attributed to strong binding between Hg(II) and the thiol ( SH) functional groups on cells and validated by experiments in which the sorbed Hg(II) was readily exchanged by thiols (e.g., glutathione) but not by carboxylic ligands such as ethylenediaminetetraacetate (EDTA). We suggest that coupled Hg(II)-cell interactions, i.e., reduction and surface binding, could be important in controlling Hg species transformation and bioavailability and should therefore be considered in microbial Hg(II) uptake and methylation studies.

Hu, Haiyan [ORNL] [ORNL; Lin, Hui [ORNL] [ORNL; Zheng, Wang [ORNL] [ORNL; Feng, Xinbin [ORNL] [ORNL; Liang, Liyuan [ORNL] [ORNL; Elias, Dwayne A [ORNL] [ORNL; Gu, Baohua [ORNL] [ORNL

2013-01-01T23:59:59.000Z

172

REDUCTION OF INHERENT MERCURY EMISSIONS IN PC COMBUSTION  

SciTech Connect (OSTI)

Mercury emission compliance presents one of the major potential challenges raised by the 1990 Clean Air Act Amendments. Simple ways of controlling emissions have not been identified. The variability in the field data suggest that inherent mercury emissions may be reduced if the source of this inherent capture can be identified and controlled. The key mechanisms appear to involve the oxidation of mercury to Hg{sup 2}, generally producing the more reactive HgCl{sub 2}, followed by its capture by certain components of the fly ash or char, or in the air pollution control equipment. This research focuses on identifying the rate-limiting steps associated with the oxidation step. Work in this reporting period focused on the refinement of the rate constants used in the kinetic mechanism for mercury oxidation. The possible reactions leading to mercury oxidation are reviewed. Rate constants for these reactions are discussed, using both literature sources and detailed estimates. The resulting mechanism represents the best present picture of the overall chlorine homogeneous oxidation chemistry. Application of this mechanism to the data will be explored in the subsequent reporting period. Work conducted under the present grant has been the subject of two meeting papers presented during the reporting period (Sliger et al., 1998a,b).

John C. Kramlich; Rebecca N. Sliger; David J. Going

1999-08-06T23:59:59.000Z

173

Supersymmetry and {sup 198}Hg  

SciTech Connect (OSTI)

The energy spectrum and electromagnetic transition properties of the supermultiplet members with two proton fermions can be constructed using the dynamical U{sub v}(6/12) x U{sub {pi}}(6/4) extended supersymmetry. In order to investigate predictions of the two proton fermion--four neutron boson supermultiplet member {sup 198}Hg, an experiment with the HORUS cube {gamma}-ray spectrometer at the Cologne TANDEM accelerator was performed using the {sup 196}Pt({alpha},2n){sup 198}Hg reaction. By analyzing {gamma}{gamma} coincidence spectra and {gamma}{gamma} angular correlations, the required experimental data--level and decay energies, level spins and multipole mixing ratios--could be obtained. For the low-energy states, the experimental data show good agreement with theory.

Bernards, Christian; Heinze, Stefan; Jolie, Jan; Fransen, Christoph; Linnemann, Andreas; Radeck, Desiree [Institut fuer Kernphysik, Universitaet zu Koeln, Zuelpicher Strasse 77, 50937 Koeln (Germany)

2009-01-28T23:59:59.000Z

174

MERIT Hg System Final Design Review  

E-Print Network [OSTI]

MERIT Hg System Final Design Review Hg Target System Operations V.B. Graves P.T. Spampinato T Facility Constraints · No overhead lifting capability within tunnel · Modularity required - Component 2 (In- beam) · Baseplate & magnet will go in beam line prior to Hg system · Blocks under magnet end

McDonald, Kirk

175

Quantification of total mercury in liver and heart tissue of Harbor Seals (Phoca vitulina) from Alaska USA  

SciTech Connect (OSTI)

This study quantified the Hg levels in the liver (n=98) and heart (n=43) tissues of Harbor Seals (Phoca vitulina) (n=102) harvested from Prince William Sound and Kodiak Island Alaska. Mercury tissue dry weight (dw) concentrations in the liver ranged from 1.7 to 393 ppm dw, and in the heart from 0.19 to 4.99 ppm dw. Results of this study indicate liver and heart tissues' Hg ppm dw concentrations significantly increase with age. Male Harbor Seals bioaccumulated Hg in both their liver and heart tissues at a significantly faster rate than females. The liver Hg bioaccumulation rates between the harvest locations Kodiak Island and Prince William Sound were not found to be significantly different. On adsorption Hg is transported throughout the Harbor Seal's body with the partition coefficient higher for the liver than the heart. No significant differences in the bio-distribution (liver:heart Hg ppm dw ratios (n=38)) values were found with respect to either age, sex or geographic harvest location. In this study the age at which Hg liver and heart bioaccumulation levels become significantly distinct in male and female Harbor Seals were identified through a Tukey's analysis. Of notably concern to human health was a male Harbor Seal's liver tissue harvested from Kodiak Island region. Mercury accumulation in this sample tissue was determined through a Q-test to be an outlier, having far higher Hg concentrarion (liver 392 Hg ppm dw) than the general population sampled. - Highlights: Black-Right-Pointing-Pointer Mercury accumulation in the liver and heart of seals exceed food safety guidelines. Black-Right-Pointing-Pointer Accumulation rate is greater in males than females with age. Black-Right-Pointing-Pointer Liver mercury accumulation is greater than in the heart tissues. Black-Right-Pointing-Pointer Mercury determination by USA EPA Method 7473 using thermal decomposition.

Marino, Kady B. [Department of Chemistry, Roger Williams University, Bristol, RI 02809 (United States)] [Department of Chemistry, Roger Williams University, Bristol, RI 02809 (United States); Hoover-Miller, Anne; Conlon, Suzanne; Prewitt, Jill [Alaska SeaLife Center, City of Seward, AK (United States)] [Alaska SeaLife Center, City of Seward, AK (United States); O'Shea, Stephen K., E-mail: soshea@rwu.edu [Department of Chemistry, Roger Williams University, Bristol, RI 02809 (United States)

2011-11-15T23:59:59.000Z

176

Optical characteristics of a HgBr excilamp  

SciTech Connect (OSTI)

Optical characteristics of a coaxial HgBr excilamp on multicomponent mercury dibromide vapour mixtures with helium, nitrogen and sulfur hexafluoride are investigated under pumping by a pulse-periodic barrier discharge. Stable excilamp operation was demonstrated at a pump pulse repetition rate of 3 9 kHz. The component composition of the working system was determined, which provides a maximal average and pulsed specific radiation power of 48.8 mW cm{sup -3} and 40.6 W cm{sup -3}, respectively, at the efficiency of 7.3 % in the blue-green spectral range with the maximal radiation intensity at the wavelength of 502 nm. The reduction in the radiation power after 2.5 10{sup 6} shots is 5 %. Interpretation is given for the results of optimisation of excilamp characteristics. (optical radiation sources)

Malinina, A A; Malinin, A N; Shuaibov, A K [Uzhgorod National University, Uzhgorod (Ukraine)

2013-08-31T23:59:59.000Z

177

Chemistry of Mercury Species and Their Control in Coal Combustion  

SciTech Connect (OSTI)

The objectives for this reporting period are: 1) The study of mercury capture mechanism by using titania sorbent and ultraviolet (UV) light, and the study of structural difference between titania particle generated by both thermal Oxidation at 1000EC and by reacting with water vapor at room temperature. 2) Measurement of ultra-fine particle size distribution in flue gas after burning coal.

None

1997-08-30T23:59:59.000Z

178

Xenon in Mercury-Manganese Stars  

E-Print Network [OSTI]

Previous studies of elemental abundances in Mercury-Manganese (HgMn) stars have occasionally reported the presence of lines of the ionized rare noble gas Xe II, especially in a few of the hottest stars with Teff ~ 13000--15000 K. A new study of this element has been undertaken using observations from Lick Observatory's Hamilton Echelle Spectrograph. In this work, the spectrum synthesis program UCLSYN has been used to undertake abundance analysis assuming LTE. We find that in the Smith & Dworetsky sample of HgMn stars, Xe is vastly over-abundant in 21 of 22 HgMn stars studied, by factors of 3.1--4.8 dex. There does not appear to be a significant correlation of Xe abundance with Teff. A comparison sample of normal late B stars shows no sign of Xe II lines that could be detected, consistent with the expected weakness of lines at normal abundance. The main reason for the previous lack of widespread detection in HgMn stars is probably due to the strongest lines being at longer wavelengths than the photographic blue. The lines used in this work were 4603.03A, 4844.33A and 5292.22A.

M. M. Dworetsky; J. L. Persaud; K. Patel

2008-01-16T23:59:59.000Z

179

EVALUATION OF MERCURY EMISSIONS FROM COAL-FIRED FACILITIES WITH SCR AND FGD SYSTEMS  

SciTech Connect (OSTI)

CONSOL Energy Inc., Research & Development (CONSOL), with support from the U.S. Department of Energy, National Energy Technology Laboratory (DOE) is evaluating the effects of selective catalytic reduction (SCR) on mercury (Hg) capture in coal-fired plants equipped with an electrostatic precipitator (ESP) - wet flue gas desulfurization (FGD) combination or a spray dyer absorber--fabric filter (SDA-FF) combination. In this program CONSOL is determining mercury speciation and removal at 10 coal-fired facilities. The objectives are (1) to evaluate the effect of SCR on mercury capture in the ESP-FGD and SDA-FF combinations at coal-fired power plants, (2) evaluate the effect of catalyst degradation on mercury capture; (3) evaluate the effect of low load operation on mercury capture in an SCR-FGD system, and (4) collect data that could provide the basis for fundamental scientific insights into the nature of mercury chemistry in flue gas, the catalytic effect of SCR systems on Hg speciation and the efficacy of different FGD technologies for Hg capture. This document, the second in a series of topical reports, describes the results and analysis of mercury sampling performed on a 330 MW unit burning a bituminous coal containing 1.0% sulfur. The unit is equipped with a SCR system for NOx control and a spray dryer absorber for SO{sub 2} control followed by a baghouse unit for particulate emissions control. Four sampling tests were performed in March 2003. Flue gas mercury speciation and concentrations were determined at the SCR inlet, air heater outlet (ESP inlet), and at the stack (FGD outlet) using the Ontario Hydro method. Process stream samples for a mercury balance were collected to coincide with the flue gas measurements. Due to mechanical problems with the boiler feed water pumps, the actual gross output was between 195 and 221 MW during the tests. The results showed that the SCR/air heater combination oxidized nearly 95% of the elemental mercury. Mercury removal, on a coal-to-stack basis, was 87%. The mercury material balance closures for the four tests conducted at the plant ranged from 89% to 114%, with an average of 100%. These results appear to show that the SCR had a positive effect on mercury removal. In earlier programs, CONSOL sampled mercury at six plants with wet FGDs for SO{sub 2} control without SCR catalysts. At those plants, an average of 61 {+-} 15% of the mercury was in the oxidized form at the air heater outlet. The principal purpose of this work is to develop a better understanding of the potential Hg removal ''co-benefits'' achieved by NOx, and SO{sub 2} control technologies. It is expected that this data will provide the basis for fundamental scientific insights into the nature of Hg chemistry in flue gas, the catalytic effect of SCR systems on Hg speciation and the efficacy of different FGD technologies for Hg capture. Ultimately, this insight could help to design and operate SCR and FGD systems to maximize Hg removal.

J. A. Withum; S.C. Tseng; J. E. Locke

2004-10-31T23:59:59.000Z

180

The removal of mercury from solid mixed waste using chemical leaching processes  

SciTech Connect (OSTI)

The focus of this research was to evaluate chemical leaching as a technique to treat soils, sediments, and glass contaminated with either elemental mercury or a combination of several mercury species. Potassium iodide/iodine solutions were investigated as chemical leaching agents for contaminated soils and sediments. Clean, synthetic soil material and surrogate storm sewer sediments contaminated with mercury were treated with KI/I{sub 2} solutions. It was observed that these leaching solutions could reduce the mercury concentration in soil and sediments by 99.8%. Evaluation of selected posttreatment sediment samples revealed that leachable mercury levels in the treated solids exceeded RCRA requirements. The results of these studies suggest that KI/I{sub 2} leaching is a treatment process that can be used to remove large quantities of mercury from contaminated soils and sediments and may be the only treatment required if treatment goals are established on Hg residual concentrations in solid matrices. Fluorescent bulbs were used to simulate mercury contaminated glass mixed waste. To achieve mercury contamination levels similar to those found in larger bulbs such as those used in DOE facilities a small amount of Hg was added to the crushed bulbs. The most effective agents for leaching mercury from the crushed fluorescent bulbs were KI/I{sub 2}, NaOCl, and NaBr + acid. Radionuclide surrogates were added to both the EPA synthetic soil material and the crushed fluorescent bulbs to determine the fate of radionuclides following chemical leaching with the leaching agents determined to be the most promising. These experiments revealed that although over 98% of the dosed mercury solubilized and was found in the leaching solution, no Cerium was measured in the posttreatment leaching solution. This finding suggest that Uranium, for which Ce was used as a surrogate, would not solubilize during leaching of mercury contaminated soil or glass.

Gates, D.D.; Chao, K.K.; Cameron, P.A.

1995-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

Removal of Elemental Mercury from a Gas Stream Facilitated by a Non-Thermal Plasma Device  

SciTech Connect (OSTI)

Mercury generated from anthropogenic sources presents a difficult environmental problem. In comparison to other toxic metals, mercury has a low vaporization temperature. Mercury and mercury compounds are highly toxic, and organic forms such as methyl mercury can be bio-accumulated. Exposure pathways include inhalation and transport to surface waters. Mercury poisoning can result in both acute and chronic effects. Most commonly, chronic exposure to mercury vapor affects the central nervous system and brain, resulting in neurological damage. The CRE technology employs a series of non-thermal, plasma-jet devices to provide a method for elemental mercury removal from a gas phase by targeting relevant chemical reactions. The technology couples the known chemistry of converting elemental mercury to ionic compounds by mercury-chlorine-oxygen reactions with the generation of highly reactive species in a non-thermal, atmospheric, plasma device. The generation of highly reactive metastable species in a non-thermal plasma device is well known. The introduction of plasma using a jet-injection device provides a means to contact highly reactive species with elemental mercury in a manner to overcome the kinetic and mass-transfer limitations encountered by previous researchers. To demonstrate this technology, WRI has constructed a plasma test facility that includes plasma reactors capable of using up to four plasma jets, flow control instrumentation, an integrated control panel to operate the facility, a mercury generation system that employs a temperature controlled oven and permeation tube, combustible and mercury gas analyzers, and a ductless fume hood designed to capture fugitive mercury emissions. Continental Research and Engineering (CR&E) and Western Research Institute (WRI) successfully demonstrated that non-thermal plasma containing oxygen and chlorine-oxygen reagents could completely convert elemental mercury to an ionic form. These results demonstrate potential the application of this technology for removing elemental mercury from flue gas streams generated by utility boilers. On an absolute basis, the quantity of reagent required to accomplish the oxidation was small. For example, complete oxidation of mercury was accomplished using a 1% volume fraction of oxygen in a nitrogen stream. Overall, the tests with mercury validated the most useful aspect of the CR&E technology: Providing a method for elemental mercury removal from a gas phase by employing a specific plasma reagent to either increase reaction kinetics or promote reactions that would not have occurred under normal circumstances.

Charles Mones

2006-12-01T23:59:59.000Z

182

Method and apparatus to measure vapor pressure in a flow system  

DOE Patents [OSTI]

The present invention is directed to a method for determining, by a condensation method, the vapor pressure of a material with a known vapor pressure versus temperature characteristic, in a flow system particularly in a mercury isotope enrichment process. 2 figures.

Grossman, M.W.; Biblarz, O.

1991-10-15T23:59:59.000Z

183

Phases of underpotentially deposited Hg on Au(111): An in situ surface X-ray diffraction study  

SciTech Connect (OSTI)

We report on an in situ surface X-ray diffraction study of the underpotential deposition (UPD) of mercury on Au(111). We have observed three UPD phases present at potentials prior to bulk mercury deposition. These phases consist of two well-ordered intermediate states and what appears to be either a fully discharged two-dimensional liquid Hg layer or a monolayer of an amorphous Hg-Au alloy. Both ordered intermediate phases have hexagonal structures with lattice vectors that are rotated 30{degree} from those of the Au(111) substrate. The first phase (phase I), present at a potential of +0.68 V, was only observed on fresh flame-annealed Au(111) electrodes and appears to be an open incommensurate structure with a lattice constant of 3.86 {+-} 0.03 A. This phase appears to be metastable since it changes to a second ordered phase (phase II) after a certain time. The second phase has a more compact lattice with a = 3.34 {+-} 0.01 A and appears to be a commensurate 2x2 structure with 2/3 of the Hg atoms at threefold hollow sites and 1/3 on atop sites. Similar to the first one, this phase is also metastable and can be transformed to a final, fully discharged, state of a two-dimensional liquid Hg layer or an amorphous Hg-Au alloy. The entire Hg UPD process, from Hg{sup 2+} to the fully discharged metallic Hg layer, agrees well with a multistep mechanism based on previous electrochemical kinetic studies on polycrystalline Au electrodes. 31 refs., 10 figs., 2 tabs.

Li, J.; Abruna, H.D. [Cornell Univ., Ithaca, NY (United States)] [Cornell Univ., Ithaca, NY (United States)

1997-04-10T23:59:59.000Z

184

Bioaccumulation of Mercury in Sharks  

E-Print Network [OSTI]

Bioaccumulation of Mercury in Sharks Part 1 b After you finish the video and the above questions Resources: EPA General Info on Mercury - http://www.epa.gov/mercury/about.htm FDA Mercury Levels in Seafood.htm World Health Organization Key Facts on Mercury - http://www.who.int/mediacentre/factsheets/fs361

Miami, University of

185

The relative importance of chlorine and bromine radicals in the oxidation of atmospheric mercury at Barrow, Alaska  

E-Print Network [OSTI]

is a naturally occurring heavy metal in the environment found globally in the air, oceans and soils et al., 2008]. Unlike other heavy metals, elemental mercury is a liquid metal with a high vapor November 2011; accepted 18 December 2011; published 3 March 2012. [1] Mercury is a toxic environmental

186

Glutathione Complex Formation With Mercury(Ii) in Aqueous Solution at Physiological Ph  

SciTech Connect (OSTI)

The mercury(II) complexes formed in neutral aqueous solution with glutathione (GSH, here denoted AH{sub 3} in its triprotonated form) were studied using Hg L{sub III}-edge extended X-ray absorption fine structure (EXAFS) and {sup 199}Hg NMR spectroscopy, complemented with electrospray ionization mass spectrometric (ESI-MS) analyses. The [Hg(AH){sub 2}]{sup 2-} complex, with the Hg-S bond distances at 2.325 {+-} 0.01 {angstrom} in linear S-Hg-S coordination, and the {sup 199}Hg NMR chemical shift at -984 ppm, dominates except at high excess of glutathione. In a series of solutions with C{sub Hg(II)} {approx} 17 mM and GSH/Hg(II) mole ratios rising from 2.4 to 11.8, the gradually increasing mean Hg-S bond distance corresponds to an increasing amount of the [Hg(AH){sub 3}]{sup 4-} complex. ESI-MS peaks appear at -m/z values of 1208 and 1230 corresponding to the [Na{sub 4}Hg(AH){sub 2}(A)]{sup -} and [Na{sub 5}Hg(AH)(A){sub 2}]{sup -} species, respectively. In another series of solutions at pH 7.0 with CHg(II) 50 mM and GSH/Hg(II) ratios from 2.0 to 10.0, the Hg L{sub III}-edge EXAFS and {sup 199}Hg NMR spectra show that at high excess of glutathione (0.35 M) about 70% of the total mercury(II) concentration is present as the [Hg(AH){sub 3}]4- complex, with the average Hg-S bond distance 2.42 {+-} 0.02 {angstrom} in trigonal HgS{sub 3} coordination. The proportions of HgSn species, n = 2, 3, and 4, quantified by fitting linear combinations of model EXAFS oscillations to the experimental EXAFS data in our present and previous studies were used to obtain stability constants for the [Hg(AH){sub 3}]{sup 4-} complex and also for the [Hg(A){sub 4}]{sup 10-} complex that is present at high pH. For Hg(II) in low concentration at physiological conditions (pH 7.4, C{sub GSH} = 2.2 mM), the relative amounts of the HgS{sub 2} species [Hg(AH){sub 2}]{sup 2-}, [Hg(AH)(A)]{sup 3-}, and the HgS{sub 3} complex [Hg(AH){sub 3}]{sup 4-} were calculated to be 95:2:3. Our results are not consistent with the formation of dimeric Hg(II)-GSH complexes proposed in a recent EXAFS study.

Mah, V.; Jalilehvand, F.; /SLAC

2012-08-23T23:59:59.000Z

187

Kinetics of Mercury(II) Adsorption and Desorption on Soil  

E-Print Network [OSTI]

Kinetics of Mercury(II) Adsorption and Desorption on Soil Y U J U N Y I N , H E R B E R T E . A L L of Delaware, Newark, Delaware 19716 D O N A L D L . S P A R K S Department of Plant and Soil Sciences kinetics of Hg(II) on four soils at pH 6 were investigated to discern the mechanisms controlling

Sparks, Donald L.

188

Source-attribution for atmospheric mercury deposition: Where does the mercury in mercury deposition come from?  

E-Print Network [OSTI]

1 Source-attribution for atmospheric mercury deposition: Where does the mercury in mercury of the Mercury Working Group, Office of Air Quality, Indiana Department of Environmental Management (IDEM) April 21, 2005 #12;2 For mercury, how important is atmospheric deposition relative to other loading

189

Mercury Reduction and Removal from High Level Waste at the Defense Waste Processing Facility - 12511  

SciTech Connect (OSTI)

The Defense Waste Processing Facility processes legacy nuclear waste generated at the Savannah River Site during production of enriched uranium and plutonium required by the Cold War. The nuclear waste is first treated via a complex sequence of controlled chemical reactions and then vitrified into a borosilicate glass form and poured into stainless steel canisters. Converting the nuclear waste into borosilicate glass is a safe, effective way to reduce the volume of the waste and stabilize the radionuclides. One of the constituents in the nuclear waste is mercury, which is present because it served as a catalyst in the dissolution of uranium-aluminum alloy fuel rods. At high temperatures mercury is corrosive to off-gas equipment, this poses a major challenge to the overall vitrification process in separating mercury from the waste stream prior to feeding the high temperature melter. Mercury is currently removed during the chemical process via formic acid reduction followed by steam stripping, which allows elemental mercury to be evaporated with the water vapor generated during boiling. The vapors are then condensed and sent to a hold tank where mercury coalesces and is recovered in the tank's sump via gravity settling. Next, mercury is transferred from the tank sump to a purification cell where it is washed with water and nitric acid and removed from the facility. Throughout the chemical processing cell, compounds of mercury exist in the sludge, condensate, and off-gas; all of which present unique challenges. Mercury removal from sludge waste being fed to the DWPF melter is required to avoid exhausting it to the environment or any negative impacts to the Melter Off-Gas system. The mercury concentration must be reduced to a level of 0.8 wt% or less before being introduced to the melter. Even though this is being successfully accomplished, the material balances accounting for incoming and collected mercury are not equal. In addition, mercury has not been effectively purified and collected in the Mercury Purification Cell (MPC) since 2008. A significant cleaning campaign aims to bring the MPC back up to facility housekeeping standards. Two significant investigations are being undertaken to restore mercury collection. The SMECT mercury pump has been removed from the tank and will be functionally tested. Also, research is being conducted by the Savannah River National Laboratory to determine the effects of antifoam addition on the behavior of mercury. These path forward items will help us better understand what is occurring in the mercury collection system and ultimately lead to an improved DWPF production rate and mercury recovery rate. (authors)

Behrouzi, Aria [Savannah River Remediation, LLC (United States); Zamecnik, Jack [Savannah River National Laboratory, Aiken, South Carolina, 29808 (United States)

2012-07-01T23:59:59.000Z

190

Decreasing aqueous mercury concentrations to achieve safe levels in fish: examining the water-fish relationship in two point-source contaminated streams  

SciTech Connect (OSTI)

East Fork Poplar Creek (EFPC) and White Oak Creek (WOC) are two mercury-contaminated streams located on the Department of Energy s Oak Ridge Reservation in east Tennessee. East Fork Poplar Creek is the larger and more contaminated of the two, with average aqueous mercury (Hg) concentrations exceeding those in reference streams by several hundred-fold. Remedial actions over the past 20 years have decreased aqueous Hg concentrations in EFPC by 85 %. Fish fillet concentrations, however, have not responded to this decrease in aqueous Hg and remain above the U.S. Environmental Protection Agency s ambient water quality criterion (AWQC) of 0.3 mg/kg. The lack of correlation between aqueous and fish tissue Hg concentrations in this creek has led to questions regarding the usefulness of target aqueous Hg concentrations and strategies for future remediation efforts. White Oak Creek has a similar contamination history but aqueous Hg concentrations in WOC are an order of magnitude lower than in EFPC. Despite the lower aqueous Hg concentrations, fish fillet concentrations in WOC have also been above the AWQC, making the most recent aqueous Hg target of 200 ng/L in EFPC seem unlikely to result in an effective decrease in fillet Hg concentrations. Recent monitoring efforts in WOC, however, suggest an aqueous total Hg threshold above which Hg bioaccumulation in fish may not respond. This new information could be useful in guiding remedial actions in EFPC and in other point-source contaminated streams.

Mathews, Teresa J [ORNL; Southworth, George R [ORNL; Peterson, Mark J [ORNL; Roy, W Kelly [ORNL; Ketelle, Richard H [ORNL; Valentine, Charles S [ORNL; Gregory, Scott M [ORNL

2013-01-01T23:59:59.000Z

191

Process for low mercury coal  

DOE Patents [OSTI]

A process for producing low mercury coal during precombustion procedures by releasing mercury through discriminating mild heating that minimizes other burdensome constituents. Said mercury is recovered from the overhead gases by selective removal.

Merriam, Norman W. (Laramie, WY); Grimes, R. William (Laramie, WY); Tweed, Robert E. (Laramie, WY)

1995-01-01T23:59:59.000Z

192

Process for low mercury coal  

DOE Patents [OSTI]

A process is described for producing low mercury coal during precombustion procedures by releasing mercury through discriminating mild heating that minimizes other burdensome constituents. Said mercury is recovered from the overhead gases by selective removal. 4 figures.

Merriam, N.W.; Grimes, R.W.; Tweed, R.E.

1995-04-04T23:59:59.000Z

193

Qualification of the Nippon Instrumentation for use in Measuring Mercury at the Defense Waste Processing Facility  

SciTech Connect (OSTI)

The Nippon Mercury/RA-3000 system installed in 221-S M-14 has been qualified for use. The qualification was a side-by-side comparison of the Nippon Mercury/RA-3000 system with the currently used Bacharach Mercury Analyzer. The side-by-side testing included standards for instrument calibration verifications, spiked samples and unspiked samples. The standards were traceable back to the National Institute of Standards and Technology (NIST). The side-by-side work included the analysis of Sludge Receipt and Adjustment Tank (SRAT) Receipt, SRAT Product, and Slurry Mix Evaporator (SME) samples. With the qualification of the Nippon Mercury/RA-3000 system in M-14, the DWPF lab will be able to perform a head to head comparison of a second Nippon Mercury/RA-3000 system once the system is installed. The Defense Waste Processing Facility (DWPF) analyzes receipt and product samples from the Sludge Receipt and Adjustment Tank (SRAT) to determine the mercury (Hg) concentration in the sludge slurry. The SRAT receipt is typically sampled and analyzed for the first ten SRAT batches of a new sludge batch to obtain an average Hg concentration. This average Hg concentration is then used to determine the amount of steam stripping required during the concentration/reflux step of the SRAT cycle to achieve a less than 0.6 wt% Hg in the SRAT product solids. After processing is complete, the SRAT product is sampled and analyzed for mercury to ensure that the mercury concentration does not exceed the 0.45 wt% limit in the Slurry Mix Evaporator (SME). The DWPF Laboratory utilizes Bacharach Analyzers to support these Hg analyses at this facility. These analyzers are more than 10 years old, and they are no longer supported by the manufacturer. Due to these difficulties, the Bacharach Analyzers are to be replaced by new Nippon Mercury/RA-3000 systems. DWPF issued a Technical Task Request (TTR) for the Savannah River National Laboratory (SRNL) to assist in the qualification of the new systems. SRNL prepared a task technical and quality assurance (TT&QA) plan that outlined the activities that are necessary and sufficient to meet the objectives of the TTR. In addition, TT&QA plan also included a test plan that provided guidance to the DWPF Lab in collecting the data needed to qualify the new Nippon Mercury/RA-3000 systems.

Edwards, T.; Mahannah, R.

2011-07-05T23:59:59.000Z

194

JV Task 126 - Mercury Control Technologies for Electric Utilities Burning Bituminous Coal  

SciTech Connect (OSTI)

The EERC developed an applied research consortium project to test cost-effective mercury (Hg) control technologies for utilities burning bituminous coals. The project goal was to test innovative Hg control technologies that have the potential to reduce Hg emissions from bituminous coal-fired power plants by {ge}90% at costs of one-half to three-quarters of current estimates for activated carbon injection (ACI). Hg control technology evaluations were performed using the EERC's combustion test facility (CTF). The CTF was fired on pulverized bituminous coals at 550,000 Btu/hr (580 MJ/hr). The CTF was configured with the following air pollution control devices (APCDs): selective catalytic reduction (SCR) unit, electrostatic precipitator (ESP), and wet flue gas desulfurization system (WFDS). The Hg control technologies investigated as part of this project included ACI (three Norit Americas, Inc., and eleven Envergex sorbents), elemental mercury (Hg{sup 0}) oxidation catalysts (i.e., the noble metals in Hitachi Zosen, Cormetech, and Hitachi SCR catalysts), sorbent enhancement additives (SEAs) (a proprietary EERC additive, trona, and limestone), and blending with a Powder River Basin (PRB) subbituminous coal. These Hg control technologies were evaluated separately, and many were also tested in combination.

Jason Laumb; John Kay; Michael Jones; Brandon Pavlish; Nicholas Lentz; Donald McCollor; Kevin Galbreath

2009-03-29T23:59:59.000Z

195

Mercury Chamber Considerations  

E-Print Network [OSTI]

Mercury Chamber Considerations V. Graves IDS-NF Target Studies July 2011 #12;2 Managed by UT-Battelle for the U.S. Department of Energy Mercury Chamber Considerations, July 2011 Flow Loop Review · 1 cm dia nozzle, 20 m/s jet requires 1.57 liter/sec mercury flow (94.2 liter/min, 24.9 gpm). · MERIT experiment

McDonald, Kirk

196

MERCURY REMOVAL IN A NON-THERMAL, PLASMA-BASED MULTI-POLLUTANT CONTROL TECHNOLOGY FOR UTILITY BOILERS  

SciTech Connect (OSTI)

This technical report describes the results from Task 1 of the Cooperative Agreement. Powerspan has installed, tested, and validated Hg SCEMS systems for measuring oxidized and elemental mercury at the pilot facility at R.E. Burger Generating Station in Shadyside, Ohio. When operating properly, these systems are capable of providing near real-time monitoring of inlet and outlet gas flow streams and are capable of extracting samples from different locations to characterize mercury removal at these different ECO process stages. This report discusses the final configuration of the Hg CEM systems and the operating protocols that increase the reliability of the HG SCEM measurements. Documentation on the testing done to verify the operating protocols is also provided. In addition the report provides details on the protocols developed and used for measurement of mercury in process liquid streams and in captured ash.

Matthew B. Loomis

2004-05-01T23:59:59.000Z

197

REDUCTION OF INHERENT MERCURY EMISSIONS IN PC COMBUSTION  

SciTech Connect (OSTI)

Mercury emission compliance presents one of the major potential challenges raised by the 1990 Clean Air Act Amendments. Simple ways of controlling emissions have not been identified. The variability in the field data suggest that inherent mercury emissions may be reduced if the source of this inherent capture can be identified and controlled. The key mechanisms appear to involve the oxidation of mercury to Hg{sup 2}, generally producing the more reactive HgCl{sub 2}, followed by its capture by certain components of the fly ash or char, or in the air pollution control equipment. This research focuses on identifying the rate-limiting steps associated with the oxidation step. Work in this reporting period focused on testing of the kinetic mechanism reported in the previous semiannual report, and the interpretation of data (both ours and literature). This model yields good qualitative agreement with the data and indicates that mercury oxidation occurs during the thermal quench of the combustion gases. The model also suggests that atomic chlorine is the key oxidizing species. The oxidation is limited to a temperature window between 700-400 C that is defined by the overlap of (1) a region of significant superequilibrium Cl concentration, and (2) a region where oxidized mercury is favored by equilibrium. Above 700 C reverse reactions effectively limit oxidized mercury concentrations. Below 400 C, atomic chlorine concentrations are too low to support further oxidation. The implication of these results are that homogeneous oxidation is governed primarily by (1) HCl concentration, (2) quench rate, and (3) background gas composition. Work conducted under the present grant has been the subject of one journal paper that was accepted for publication during the reporting period (Sliger et al., 1999).

John C. Kramlich; Rebecca N. Sliger; David J. Going

1999-08-06T23:59:59.000Z

198

Pre-Colombian Mercury Pollution Associated with the Smelting of Argentiferous Ores in the Bolivian Andes  

E-Print Network [OSTI]

large-scale Hg emissions. Pre-industrial emissions of heavy metals associated with mineral extraction) (Lee et al. 2008). In the New World, early metal pollution appears to be limited ? Royal SwedishREPORT Pre-Colombian Mercury Pollution Associated with the Smelting of Argentiferous Ores

Wolfe, Alexander P.

199

Mercury in the Global Atmosphere: Chemistry, deposition, and land-atmosphere interactions  

E-Print Network [OSTI]

climate scientists can learn from Hg pollution oror Coauthors/collaborators: D.J. Jacob, E. M. Sunderland. Conn) #12;A science and policy challengeA science and policy challenge Mercury in polar bear fur up 5, 2006; Selin and Jacob, 2008] #12;Policy challenges across temporal scales Use source

Selin, Noelle Eckley

200

Anutritional dilemma: fish consumption, mercury exposure and growth of children in  

E-Print Network [OSTI]

Bolivia Authors: Eric Benefice a ; Selma J. Luna Monrroy b ; Ronald W. Lopez Rodriguez c Affiliation s, La Paz, Bolivia c IRD, UR024, Epidemiology and Prevention, La Paz, Bolivia DOI: 10 Amerindian communities in the Beni River valley (Amazonian Bolivia). Hair mercury content (H-Hg) served

Paris-Sud XI, Universit de

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


201

Evaluation of Sorbent Injection for Mercury Control  

SciTech Connect (OSTI)

The power industry in the U.S. is faced with meeting new regulations to reduce the emissions of mercury compounds from coal-fired plants. These regulations are directed at the existing fleet of nearly 1,100 boilers. These plants are relatively old with an average age of over 40 years. Although most of these units are capable of operating for many additional years, there is a desire to minimize large capital expenditures because of the reduced (and unknown) remaining life of the plant to amortize the project. Injecting a sorbent such as powdered activated carbon into the flue gas represents one of the simplest and most mature approaches to controlling mercury emissions from coal-fired boilers. This is the final site report for tests conducted at DTE Energy's Monroe Power Plant, one of five sites evaluated in this DOE/NETL program. The overall objective of the test program was to evaluate the capabilities of activated carbon injection at five plants: Sunflower Electric's Holcomb Station Unit 1, AmerenUE's Meramec Station Unit 2, Missouri Basin Power Project's Laramie River Station Unit 3, Detroit Edison's Monroe Power Plant Unit 4, and AEP's Conesville Station Unit 6. These plants have configurations that together represent 78% of the existing coal-fired generation plants. The goals for the program established by DOE/NETL were to reduce the uncontrolled mercury emissions by 50 to 70% at a cost 25 to 50% lower than the target established by DOE of $60,000/lb mercury removed. The results from Monroe indicate that using DARCO{reg_sign} Hg would result in higher mercury removal (80%) at a sorbent cost of $18,000/lb mercury, or 70% lower than the benchmark. These results demonstrate that the goals established by DOE/NETL were exceeded during this test program. The increase in mercury removal over baseline conditions is defined for this program as a comparison in the outlet emissions measured using the Ontario Hydro method during the baseline and long-term test periods. The change in outlet emissions from baseline to long-term testing was 81%.

Sharon Sjostrom

2006-04-30T23:59:59.000Z

202

EVALUATION OF MERCURY EMISSIONS FROM COAL-FIRED FACILITIES WITH SCR AND FGD SYSTEMS  

SciTech Connect (OSTI)

CONSOL Energy Inc., Research & Development (CONSOL), with support from the U.S. Department of Energy, National Energy Technology Laboratory (DOE) and the Electric Power Research Institute (EPRI), is evaluating the effects of selective catalytic reduction (SCR) on mercury (Hg) capture in coal-fired plants equipped with an electrostatic precipitator (ESP)--wet flue gas desulfurization (FGD) combination or a spray dryer absorber--fabric filter (SDA-FF) combination. In this program CONSOL is determining mercury speciation and removal at 10 coal-fired facilities. The objectives are (1) to evaluate the effect of SCR on mercury capture in the ESP-FGD and SDA-FF combinations at coal-fired power plants, (2) evaluate the effect of catalyst degradation on mercury capture; (3) evaluate the effect of low load operation on mercury capture in an SCR-FGD system, and (4) collect data that could provide the basis for fundamental scientific insights into the nature of mercury chemistry in flue gas, the catalytic effect of SCR systems on mercury speciation and the efficacy of different FGD technologies for mercury capture. This document, the seventh in a series of topical reports, describes the results and analysis of mercury sampling performed on a 1,300 MW unit burning a bituminous coal containing three percent sulfur. The unit was equipped with an ESP and a limestone-based wet FGD to control particulate and SO2 emissions, respectively. At the time of sampling an SCR was not installed on this unit. Four sampling tests were performed in September 2003. Flue gas mercury speciation and concentrations were determined at the ESP outlet (FGD inlet), and at the stack (FGD outlet) using the Ontario Hydro method. Process stream samples for a mercury balance were collected to coincide with the flue gas measurements. The results show that the FGD inlet flue gas oxidized:elemental mercury ratio was roughly 2:1, with 66% oxidized mercury and 34% elemental mercury. Mercury removal, on a coal-to-stack basis, was 53%. The average Hg concentration in the stack flue gas was 4.09 {micro}g/m{sup 3}. The average stack mercury emission was 3.47 Ib/TBtu. The mercury material balance closures ranged from 87% to 108%, with an average of 97%. A sampling program similar to this one was performed on a similar unit (at the same plant) that was equipped with an SCR for NOx control. Comparison of the results from the two units show that the SCR increases the percentage of mercury that is in the oxidized form, which, in turn, lends to more of the total mercury being removed in the wet scrubber. The principal purpose of this work is to develop a better understanding of the potential mercury removal ''co-benefits'' achieved by NOx, and SO{sub 2} control technologies. It is expected that this data will provide the basis for fundamental scientific insights into the nature of mercury chemistry in flue gas, the catalytic effect of SCR systems on mercury speciation and the efficacy of different FGD technologies for mercury capture. Ultimately, this insight could help to design and operate SCR and FGD systems to maximize mercury removal.

J.A. Withum; S.C. Tseng; J.E. Locke

2005-11-01T23:59:59.000Z

203

Process for combined control of mercury and nitric oxide.  

SciTech Connect (OSTI)

Continuing concern about the effects of mercury in the environment may lead to requirements for the control of mercury emissions from coal-fired power plants. If such controls are mandated, the use of existing flue-gas cleanup systems, such as wet scrubbers currently employed for flue-gas desulfurization, would be desirable, Such scrubbers have been shown to be effective for capturing oxidized forms of mercury, but cannot capture the very insoluble elemental mercury (Hg{sup 0}) that can form a significant fraction of the total emissions. At Argonne National Laboratory, we have proposed and tested a concept for enhancing removal of Hg{sup 0}, as well as nitric oxide, through introduction of an oxidizing agent into the flue gas upstream of a scrubber, which readily absorbs the soluble reaction products. Recently, we developed a new method for introducing the oxidizing agent into the flue-gas stream that dramatically improved reactant utilization. The oxidizing agent employed was NOXSORB{trademark}, which is a commercial product containing chloric acid and sodium chlorate. When a dilute solution of this agent was introduced into a gas stream containing Hg{sup 0} and other typical flue-gas species at 300 F, we found that about 100% of the mercury was removed from the gas phase and recovered in process liquids. At the same time, approximately 80% of the nitric oxide was removed. The effect of sulfur dioxide on this process was also investigated and the results showed that it slightly decreased the amount of Hg{sup 0} oxidized while appearing to increase the removal of nitric oxide from the gas phase. We are currently testing the effects of variations in NOXSORB{trademark} concentration, sulfur dioxide concentration, nitric oxide concentration, and reaction time (residence time). Preliminary economic projections based on the results to date indicate that the chemical cost for nitric oxide oxidation could be less than $5,000/ton removed, while for Hg{sup 0} oxidation it would be about $20,000/lb removed.

Livengood, C. D.; Mendelsohn, M. H.

1999-11-03T23:59:59.000Z

204

Automated product recovery in a Hg-196 photochemical isotope separation process  

DOE Patents [OSTI]

A method of removing deposited product from a photochemical reactor used in the enrichment of [sup 196]Hg has been developed and shown to be effective for rapid re-cycling of the reactor system. Unlike previous methods relatively low temperatures are used in a gas and vapor phase process of removal. Importantly, the recovery process is understood in a quantitative manner so that scaling design to larger capacity systems can be easily carried out. 2 figs.

Grossman, M.W.; Speer, R.

1992-07-21T23:59:59.000Z

205

Direct Measurement of Mercury Reactions In Coal Power Plant Plumes  

SciTech Connect (OSTI)

Recent field and pilot-scale results indicate that divalent mercury emitted from power plants may rapidly transform to elemental mercury within the power plant plumes. Simulations of mercury chemistry in plumes based on measured rates to date have improved regional model fits to Mercury Deposition Network wet deposition data for particular years, while not degrading model verification fits for remaining years of the ensemble. The years with improved fit are those with simulated deposition in grid cells in the State of Pennsylvania that have matching MDN station data significantly less than the model values. This project seeks to establish a full-scale data basis for whether or not significant reduction or oxidation reactions occur to mercury emitted from coal-fired power plants, and what numerical redox rate should apply for extension to other sources and for modeling of power plant mercury plumes locally, regionally, and nationally. Although in-stack mercury (Hg) speciation measurements are essential to the development of control technologies and to provide data for input into atmospheric fate and transport models, the determination of speciation in a cooling coal combustion plume is more relevant for use in estimating Hg fate and effects through the atmosphere. It is mercury transformations that may occur in the plume that determine the eventual rate and patterns of mercury deposited to the earth's surface. A necessary first step in developing a supportable approach to modeling any such transformations is to directly measure the forms and concentrations of mercury from the stack exit downwind to full dispersion in the atmosphere. As a result, a study was sponsored by EPRI and jointly funded by EPRI, the U.S Department of Energy (DOE), and the Wisconsin Department of Administration. The study was designed to further our understanding of plume chemistry. The study was carried out at the We Energies Pleasant Prairie Power Plant, Pleasant Prairie, Wisconsin, just west of Kenosha. Aircraft and ground measurements support the occurrence of a reduction in the fraction of reactive gaseous mercury (RGM) (with a corresponding increase in elemental mercury) as part of the Total Gaseous Mercury (TGM) emitted from the Pleasant Prairie stack. This occurrence is based on comparison of the RGM concentrations in the plume (at standard conditions) compared to the RGM in the stack. There was found to be a 44% drop in the fraction of RGM between the stack exit and the first sampling arc and a 66% reduction from the stack to the 5-mile sampling arc, with no additional drop between the 5- and 10-mile arcs. Smaller-scale experiments in both test chambers and pilot-scale coal combustor exhaust streams have indicated the presence of rapid and relatively complete reduction reactions converting divalent into elemental mercury within power plant plumes prior to full dispersion in the atmosphere. These measurements, however, have been unable to identify whether the reactions occur during plume rise from physical to virtual stack height (during positive thermal buoyancy). The presence, rate, completeness, ubiquity, and dependence on source characteristics of these reactions, however, must be demonstrated in plume environments associated with fully operational power plants. That requirement, to capture either the reactions or the reaction products of chemistry that may be occurring very close to stack exits in highly turbulent environments, constrains the precision and reproducibility with which such full-scale experiments can be carried out. The work described here is one of several initial steps required to test whether, and in what direction, such rapid mercury redox reactions might be occurring in such plumes.

Leonard Levin

2005-12-31T23:59:59.000Z

206

Target System Operations and Hg Handling  

E-Print Network [OSTI]

CERN June 19-20, 2006 #12;2 OAK RIDGE NATIONAL LABORATORY U. S. DEPARTMENT OF ENERGY Hg System Safety RIDGE NATIONAL LABORATORY U. S. DEPARTMENT OF ENERGY Hg System Safety Review 19-20 June 2006 Containment/vent ports will be soap- bubble checked Primary Enclosure Secondary Enclosure #12;4 OAK RIDGE NATIONAL

McDonald, Kirk

207

Characterization of the Deltaproteobacteria in contaminated and uncontaminated stream sediments and identification of potential mercury methylators  

SciTech Connect (OSTI)

Microbial communities were examined in surface stream sediments at 5 contaminated sites and 1 control site near Oak Ridge, TN, USA, to identify bacteria that could be contributing to mercury (Hg) methylation. The phylogenetic composition of the sediment bacterial community was examined over 3 quarterly sampling periods (36 samples) using 16S rRNA gene pyrosequencing. Only 3064 sequences (0.85% of the total community) were identified as Deltaproteobacteria, the only group known to methylate Hg, using the Ribosomal Database Project classifier at the 99% confidence threshold. Constrained ordination techniques indicated statistically significant positive linear correlations between Desulfobulbus spp., Desulfonema spp. and Desulfobacca spp. and methyl-Hg concentrations at the Hg-contaminated sites. In contrast, the distribution of organisms related to Byssovorax spp. was significantly correlated to inorganic carbon, nitrate and uranium concentrations but not to Hg or methyl-Hg. Overall, the abundance and richness of Deltaproteobacteria sequences were higher in uncontaminated sediments, while the majority of the members present at the contaminated sites were either known potential metal-reducers/methylators or metal tolerant species. Given the abundance relative to other known Hg methylators and the association with methyl-Hg, Desulfobulbus spp. is considered a prime candidate for involvement in Hg methylation in these streams.

Mosher, Jennifer [ORNL; Vishnivetskaya, Tatiana A [ORNL; Elias, Dwayne A [ORNL; Podar, Mircea [ORNL; Brooks, Scott C [ORNL; Brown, Steven D [ORNL; Brandt, Craig C [ORNL; Palumbo, Anthony Vito [ORNL

2012-01-01T23:59:59.000Z

208

CERN Hg Jet System V.B. Graves  

E-Print Network [OSTI]

Collaboration Mtg 16 Feb 05 Alternative Hg Delivery System Hydraulic Fluid Cylinder (3000 psi) Hg Cylinder (1000 energy performed on piston = press*area*dist/time 11 Hyd Pump pump inefficiency 8 11 340 340 6 8 Piston Sized for 20sec jet Drain Hg Supply Hg Return Position Sensor Hydraulic Lines Hg Cylinder Vent Line #12

McDonald, Kirk

209

Neutrino Factory Mercury Vessel  

E-Print Network [OSTI]

Neutrino Factory Mercury Vessel: Initial Cooling Calculations V. Graves Target Studies Nov 15, 2012 #12;2 Managed by UT-Battelle for the U.S. Department of Energy Cooling Calculations 15 Nov 2012 Target · Separates functionality, provides double mercury containment, simplifies design and remote handling · Each

McDonald, Kirk

210

Mercury in the environment  

ScienceCinema (OSTI)

Abbott works for Idaho National Laboratory as an environmental scientist. Using state-of-thescienceequipment, he continuously samples the air, looking for mercury. In turn, he'll analyzethis long-term data and try to figure out the mercury's point of or

Idaho National Laboratory - Mike Abbott

2010-01-08T23:59:59.000Z

211

Mercury Jet Studies Tristan Davenne  

E-Print Network [OSTI]

Mercury Jet Studies Tristan Davenne Rutherford Appleton Laboratory Joint UKNF, INO, UKIERI meeting mercury target and reported a radial velocity at surface of mercury jet due to proton beam is 36m/s #12;Numerical simulation of Sievers & Pugnat Result Click on image above to watch video of 2cm mercury target

McDonald, Kirk

212

Axi-symmetrical flow reactor for [sup 196]Hg photochemical enrichment  

DOE Patents [OSTI]

The present invention is directed to an improved photochemical reactor useful for the isotopic enrichment of a predetermined isotope of mercury, especially, [sup 196]Hg. Specifically, two axi-symmetrical flow reactors were constructed according to the teachings of the present invention. These reactors improve the mixing of the reactants during the photochemical enrichment process, affording higher yields of the desired [sup 196]Hg product. Measurements of the variation of yield (Y) and enrichment factor (E) along the flow axis of these reactors indicates very substantial improvement in process uniformity compared to previously used photochemical reactor systems. In one preferred embodiment of the present invention, the photoreactor system was built such that the reactor chamber was removable from the system without disturbing the location of either the photochemical lamp or the filter employed therewith. 10 figures.

Grossman, M.W.

1991-04-30T23:59:59.000Z

213

Mercury Effects, Sources and Control Measures  

E-Print Network [OSTI]

Mercury Effects, Sources and Control Measures Prepared by Alan B. Jones, Brooks Rand, Ltd., Seattle ................................................................................................................................1 MERCURY SOURCES....................................................................................................................................................................................8 Mercury dumping from naval vessels

214

Mercury Sensing with Optically Responsive Gold Nanoparticles  

E-Print Network [OSTI]

We assume that the mass of mercury adsorbed at saturation istactics, nanoparticle based mercury sensing should advancemost sensitive method for mercury sensing. References "1!

James, Jay Zachary

2012-01-01T23:59:59.000Z

215

Characterization of mercury, arsenic, and selenium in the product streams of the Pacific Northwest Laboratory 6-kg retort  

SciTech Connect (OSTI)

The objective of this program is to determine how retorting process parameters affect the partitioning of Hg, As, Se, and Cd from raw oil shale to spent shale, shale oil, retort water, and offgas. For each of the elements, the objective of this study is to (1) determine the distribution coefficients for each product stream; (2) identify the chemical forms in water, gas, and oil streams, with particular emphasis on inorganic or organometallic species known to be or suspected of being carcinogenic, toxic, or otherwise harmful; (3) investigate the mechanism(s) responsible for mobilization into each product stream for toxic or labile chemical forms identified in item 2 are mobilized into each product stream; and (4) the effect of retorting rate, maximum retorting temperature, and retorting atmosphere on items 1 and 3. A Green River shale from Colorado and a New Albany shale from Kentucky were heated at 1 to 2/sup 0/C/min and at 10/sup 0/C/min to maximum temperatures of 500 and 750/sup 0/C under a nitrogen sweep gas. The product streams were analyzed using a variety of methods including Zeeman atomic absorption spectroscopy, microwave-induced helium plasma spectroscopy, x-ray fluorescence, instrumental neutron activation analysis, high-pressure liquid and silica gel column chromatography, and mercury cold vapor atomic absorption. The results obtained using these analytical methods indicate that the distribution of mercury, arsenic, and selenium in the product stream is a function of oil shale type, heating rates, and maximum retorting temperatures. 11 refs., 27 figs., 5 tabs.

Olsen, K.B.; Evans, J.C.; Sklarew, D.S.; Girvin, D.C.; Nelson, C.L.; Lepel, E.A.; Robertson, D.E.; Sanders, R.W.

1985-12-01T23:59:59.000Z

216

Corrosion of type 316L stainless steel in a mercury thermal convection loop  

SciTech Connect (OSTI)

Two thermal convection loops fabricated from 316L stainless steel containing mercury (Hg) and Hg with 1000 wppm gallium (Ga), respectively, were operated continuously for about 5000 h. In each case, the maximum loop temperature was constant at about 305 degrees C and the minimum temperature was constant at about 242 degrees C. Coupons in the hot leg of the Hg-loop developed a posous surface layer substantially depleted of nickel and chromium, which resulted in a transformation to ferrite. The coupon exposed at the top of the hot leg in the Hg-loop experienced the maximum degradation, exhibiting a surface layer extending an average of 9-10 mu m after almost 5000 h. Analysis of the corrosion rate data as a function of temperature (position) in the Hg-loop suggests wetting by the mer cury occurred only above about 255 degrees C and that the rate limiting step in the corrosion process above 255 degrees C is solute diffusion through the saturated liquid boundary layer adjacent to the corroding surface. The latter factor suggests that the corrosion of 316L stainless steel in a mercury loop may be velocity dependent. No wetting and no corrosion were observed on the coupons and wall specimens removed from the Hg/Ga loop after 5000 h of operation.

DiStefano, J.R.; Manneschmidt, E.T.; Pawel, S.J.

1999-04-01T23:59:59.000Z

217

Calibrated vapor generator source  

DOE Patents [OSTI]

A portable vapor generator is disclosed that can provide a controlled source of chemical vapors, such as, narcotic or explosive vapors. This source can be used to test and calibrate various types of vapor detection systems by providing a known amount of vapors to the system. The vapor generator is calibrated using a reference ion mobility spectrometer. A method of providing this vapor is described, as follows: explosive or narcotic is deposited on quartz wool, placed in a chamber that can be heated or cooled (depending on the vapor pressure of the material) to control the concentration of vapors in the reservoir. A controlled flow of air is pulsed over the quartz wool releasing a preset quantity of vapors at the outlet. 10 figs.

Davies, J.P.; Larson, R.A.; Goodrich, L.D.; Hall, H.J.; Stoddard, B.D.; Davis, S.G.; Kaser, T.G.; Conrad, F.J.

1995-09-26T23:59:59.000Z

218

CARBON BED MERCURY EMISSIONS CONTROL FOR MIXED WASTE TREATMENT  

SciTech Connect (OSTI)

Mercury has had various uses in nuclear fuel reprocessing and other nuclear processes, and so is often present in radioactive and mixed (both radioactive and hazardous according tohe Resource Conservation and Recovery Act) wastes. Depending on regulatory requirements, the mercury in the off-gas must be controlled with sometimes very high efficiencies. Compliance to the Hazardous Waste Combustor (HWC) Maximum Achievable Control Technology (MACT) standards can require off-gas mercury removal efficiencies up to 99.999% for thermally treating some mixed waste streams. Several test programs have demonstrated this level of off-gas mercury control using fixed beds of granular sulfur-impregnated activated carbon. Other results of these tests include: (a) The depth of the mercury control mass transfer zone was less than 15-30 cm for the operating conditions of these tests, (b) MERSORB carbon can sorb Hg up to 19 wt% of the carbon mass, and (c) the spent carbon retained almost all (98 99.99%) of the Hg; but when even a small fraction of the total Hg dissolves, the spent carbon can fail the TCLP test when the spent carbon contains high Hg concentrations. Localized areas in a carbon bed that become heated through heat of adsorption, to temperatures where oxidation occurs, are referred to as bed hot spots. Carbon bed hot spots must be avoided in processes that treat radioactive and mixed waste. Key to carbon bed hot spot mitigation are (a) designing for sufficient gas velocity, for avoiding gas flow maldistribution, and for sufficient but not excessive bed depth, (b) monitoring and control of inlet gas flowrate, temperature, and composition, (c) monitoring and control of in-bed and bed outlet gas temperatures, and (d) most important, monitoring of bed outlet CO concentrations. An increase of CO levels in the off-gas downstream of the carbon bed to levels about 50-100 ppm higher than the inlet CO concentration indicate CO formation in the bed, caused by carbon bed hot spots. Corrective actions must be implemented quickly if bed hot spots are detected, using a graded approach and sequence starting with corrective actions that are simple, quick, cause the least impact to the process, and are easiest to recover from. Multiple high and high-high alarm levels should be used, with appropriate corrective actions for each level.

Nick Soelberg; Joe Enneking

2010-11-01T23:59:59.000Z

219

High Power Hg Target Conceptual Design Review  

E-Print Network [OSTI]

to Hg Hg Temp Rise Input Energy (hp) Losses Lost Energy (hp) Output Energy (hp) BTU/min BTU/min BTU/min BTU/ min KW HP BTU/min F/sec Elect Motor 60 60 hp * 5% inefficiency 3 57 127 127 2 3 Mag Coupling 5 Energy (hp) BTU/min BTU/min BTU/min BTU/ min KW HP BTU/min F/sec Elect Motor 60 60 hp * 5% inef

McDonald, Kirk

220

Emissions, Monitoring, and Control of Mercury from Subbituminous Coal-Fired Power Plants - Phase II  

SciTech Connect (OSTI)

Western Research Institute (WRI), in conjunction with Western Farmers Electric Cooperative (WFEC), has teamed with Clean Air Engineering of Pittsburgh PA to conduct a mercury monitoring program at the WEFC Hugo plant in Oklahoma. Sponsored by US Department of Energy Cooperative Agreement DE-FC-26-98FT40323, the program included the following members of the Subbituminous Energy Coalition (SEC) as co-sponsors: Missouri Basin Power Project; DTE Energy; Entergy; Grand River Dam Authority; and Nebraska Public Power District. This research effort had five objectives: (1) determine the mass balance of mercury for subbituminous coal-fired power plant; (2) assess the distribution of mercury species in the flue gas (3) perform a comparison of three different Hg test methods; (4) investigate the long-term (six months) mercury variability at a subbituminous coal-fired power plant; and (5) assess operation and maintenance of the Method 324 and Horiba CEMS utilizing plant personnel.

Alan Bland; Jesse Newcomer; Allen Kephart; Volker Schmidt; Gerald Butcher

2008-10-31T23:59:59.000Z

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


221

Survey of mercury, cadmium and lead content of household batteries  

SciTech Connect (OSTI)

Highlights: A well selected sample of 146 batteries was analysed for its heavy metals content. A comparison was made between heavy metals contents in batteries in 2006 and 2011. No significant change after implementation of the new EU Batteries Directive. Severe differences in heavy metal contents were found in different battery-types. - Abstract: The objective of this work was to provide updated information on the development of the potential impact of heavy metal containing batteries on municipal waste and battery recycling processes following transposition of the new EU Batteries Directive 2006/66/EC. A representative sample of 146 different types of commercially available dry and button cells as well as lithium-ion accumulators for mobile phones were analysed for their mercury (Hg)-, cadmium (Cd)- and lead (Pb)-contents. The methods used for preparing the cells and analysing the heavy metals Hg, Cd, and Pb were either developed during a former study or newly developed. Several batteries contained higher mass fractions of mercury or cadmium than the EU limits. Only half of the batteries with mercury and/or lead fractions above the marking thresholds were labelled. Alkalinemanganese mono-cells and Li-ion accumulators, on average, contained the lowest heavy metal concentrations, while zinccarbon batteries, on average, contained the highest levels.

Recknagel, Sebastian, E-mail: sebastian.recknagel@bam.de [BAM Federal Institute for Materials Research and Testing, Department of Analytical Chemistry, Reference Materials, Richard-Willsttter-Strae 11, D-12489 Berlin (Germany); Radant, Hendrik [BAM Federal Institute for Materials Research and Testing, Department of Analytical Chemistry, Reference Materials, Richard-Willsttter-Strae 11, D-12489 Berlin (Germany); Kohlmeyer, Regina [German Federal Environment Agency (UBA), Section III 1.6 Extended Producer Responsibility, Wrlitzer Platz 1, D-06844 Dessau-Rolau (Germany)

2014-01-15T23:59:59.000Z

222

Mercury and Air Toxic Element Impacts of Coal Combustion By-Product Disposal and Utilizaton  

SciTech Connect (OSTI)

The University of North Dakota Energy & Environmental Research Center (EERC) conducted a multiyear study to evaluate the impact of mercury and other air toxic elements (ATEs) on the management of coal combustion by-products (CCBs). The ATEs evaluated in this project were arsenic, cadmium, chromium, lead, nickel, and selenium. The study included laboratory tasks to develop measurement techniques for mercury and ATE releases, sample characterization, and release experiments. A field task was also performed to measure mercury releases at a field site. Samples of fly ash and flue gas desulfurization (FGD) materials were collected preferentially from full-scale coal-fired power plants operating both without and with mercury control technologies in place. In some cases, samples from pilot- and bench-scale emission control tests were included in the laboratory studies. Several sets of 'paired' baseline and test fly ash and FGD materials collected during full-scale mercury emission control tests were also included in laboratory evaluations. Samples from mercury emission control tests all contained activated carbon (AC) and some also incorporated a sorbent-enhancing agent (EA). Laboratory release experiments focused on measuring releases of mercury under conditions designed to simulate CCB exposure to water, ambient-temperature air, elevated temperatures, and microbes in both wet and dry conditions. Results of laboratory evaluations indicated that: (1) Mercury and sometimes selenium are collected with AC used for mercury emission control and, therefore, present at higher concentrations than samples collected without mercury emission controls present. (2) Mercury is stable on CCBs collected from systems both without and with mercury emission controls present under most conditions tested, with the exception of vapor-phase releases of mercury exposed to elevated temperatures. (3) The presence of carbon either from added AC or from unburned coal can result in mercury being sorbed onto the CCB when exposed to ambient-temperature air. The environmental performance of the mercury captured on AC used as a sorbent for mercury emission control technologies indicated that current CCB management options will continue to be sufficiently protective of the environment, with the potential exception of exposure to elevated temperatures. The environmental performance of the other ATEs investigated indicated that current management options will be appropriate to the CCBs produced using AC in mercury emission controls.

David Hassett; Loreal Heebink; Debra Pflughoeft-Hassett; Tera Buckley; Erick Zacher; Mei Xin; Mae Sexauer Gustin; Rob Jung

2007-03-31T23:59:59.000Z

223

Method and apparatus for monitoring mercury emissions  

DOE Patents [OSTI]

A mercury monitoring device that continuously monitors the total mercury concentration in a gas. The device uses the same chamber for converting speciated mercury into elemental mercury and for measurement of the mercury in the chamber by radiation absorption techniques. The interior of the chamber is resistant to the absorption of speciated and elemental mercury at the operating temperature of the chamber. 15 figs.

Durham, M.D.; Schlager, R.J.; Sappey, A.D.; Sagan, F.J.; Marmaro, R.W.; Wilson, K.G.

1997-10-21T23:59:59.000Z

224

Method and apparatus for monitoring mercury emissions  

DOE Patents [OSTI]

A mercury monitoring device that continuously monitors the total mercury concentration in a gas. The device uses the same chamber for converting speciated mercury into elemental mercury and for measurement of the mercury in the chamber by radiation absorption techniques. The interior of the chamber is resistant to the absorption of speciated and elemental mercury at the operating temperature of the chamber.

Durham, Michael D. (Castle Rock, CO); Schlager, Richard J. (Aurora, CO); Sappey, Andrew D. (Golden, CO); Sagan, Francis J. (Lakewood, CO); Marmaro, Roger W. (Littleton, CO); Wilson, Kevin G. (Littleton, CO)

1997-01-01T23:59:59.000Z

225

In Situ Mercury Stabilization (ISMS) Treatment: Technology Maturation Project Phase I Status Report  

SciTech Connect (OSTI)

Mercury (Hg) was used to separate lithium-6 isotope for weapons production at the Y-12 Plant in Oak Ridge in the 1950s and 1960s. As much as two million pounds of elemental mercury was 'lost' or unaccounted for and a large portion of that material is believed to have entered the environment. The DOE site office in Oak Ridge has identified Hg pollution in soils, sediments, and streams as the most significant environmental challenge currently faced. In industry, large amounts of mercury have been used to manufacture products (e.g., fluorescent light bulbs, thermometers) and for chemical processing (e.g., production of chlorine and alkali via mercury electrochemical cells) and many of these industrial sites are now polluted with mercury contaminated soil as a result of previous releases and/or inadvertent leaks. Remediation techniques for Hg contaminated soils are either based on thermal desorption and recovery of the mercury or excavation and shipping of large volumes of material to remote facilities for treatment and disposal. Both of these alternatives are extremely costly. The Brookhaven National Laboratory (BNL) Environmental Research & Technology Division (ERTD) has demonstrated, in laboratory-scale experiments, the viability of treating mercury contaminated soils by means of sulfide treatment rods inserted into the soil through a process known as In Situ Mercury Stabilization (ISMS). This approach is partly based on BNL's patented and successfully licensed ex situ process for Hg treatment, Sulfur Polymer Stabilization/Solidification (SPSS) which converts Hg to the more stable sulfide form. The original experiments showed that Hg homogeneously distributed in soil rapidly migrates to form a high concentration zone of chemically stable mercuric sulfide near the treatment rods while concentrations of Hg in surrounding areas away from the treatment rods are depleted to acceptable levels. BSA has subsequently filed for patent protection on the ISMS technology. If further developed it has the potential for large-scale in-situ treatment of contaminated soils that could substantially reduce the prohibitive cost of thermal desorption and/or excavation and disposal. Licensing and spin-off technology development opportunities would then be viable. Depending on performance and regulatory acceptance, the treated mercury could either be excavated for disposal elsewhere or left in place as a stable alternative. Excavated spent treatment rods could be processed by the SPSS process to reduce the potential for dispersion and lower leachability even further. The Phase I objectives of the In Situ Mercury Stabilization Treatment Process Technology Maturation Project were to: (1) replicate the original bench-scale results that formed the basis for BNL's patent application, i.e., mercury contamination in soil will migrate to and react with 'rods' containing sulfur and/or sulfur compounds, (2) provide enough information to evaluate a decision to conduct further development, and (3) establish some of the critical parameters that require further technology maturation during Phase II. The information contained in this report summarizes the work conducted in Phase I to meet these objectives.

Kalb,P.D.; Milian, L.

2008-03-01T23:59:59.000Z

226

Impacts of halogen additions on mercury oxidation, in a slipstream selective catalyst reduction (SCR), reactor when burning sub-bituminous coal  

SciTech Connect (OSTI)

This paper presents a comparison of impacts of halogen species on the elemental mercury (Hg(0)) oxidation in a real coal-derived flue gas atmosphere. It is reported there is a higher percentage of Hg(0) in the flue gas when burning sub-bituminous coal (herein Powder River Basin (PRB) coal) and lignite, even with the use of selective catalytic reduction (SCR). The higher Hg(0) concentration in the flue gas makes it difficult to use the wet-FGD process for the mercury emission control in coal-fired utility boilers. Investigation of enhanced Hg(0) oxidation by addition of hydrogen halogens (HF, HCl, HBr, and HI) was conducted in a slipstream reactor with and without SCR catalysts when burning PRB coal. Two commercial SCR catalysts were evaluated. SCR catalyst no. 1 showed higher efficiencies of both NO reduction and Hg(0) oxidation than those of SCR catalyst no. 2. NH{sub 3} addition seemed to inhibit the Hg(0) oxidation, which indicated competitive processes between NH{sub 3} reduction and Hg(0) oxidation on the surface of SCR catalysts. The hydrogen halogens, in the order of impact on Hg(0) oxidation, were HBr, HI, and HCl or HF. Addition of HBr at approximately 3 ppm could achieve 80% Hg(0) oxidation. Addition of HI at approximately 5 ppm could achieve 40% Hg(0) oxidation. In comparison to the empty reactor, 40% Hg(0) oxidation could be achieved when HCl addition was up to 300 ppm. The enhanced Hg(0) oxidation by addition of HBr and HI seemed not to be correlated to the catalytic effects by both evaluated SCR catalysts. The effectiveness of conversion of hydrogen halogens to halogen molecules or interhalogens seemed to be attributed to their impacts on Hg(0) oxidation. 30 refs., 4 figs.

Yan Cao; Zhengyang Gao; Jiashun Zhu; Quanhai Wang; Yaji Huang; Chengchung Chiu; Bruce Parker; Paul Chu; Wei-ping Pan [Western Kentucky University (WKU), Bowling Green, KY (United States). Institute for Combustion Science and Environmental Technology (ICSET)

2008-01-01T23:59:59.000Z

227

SULFUR POLYMER STABILIZATION/SOLIDIFICATION (SPSS) TREATABILITY OF SIMULATED MIXED-WASTE MERCURY CONTAMINATED SLUDGE.  

SciTech Connect (OSTI)

The Environmental Protection Agency (EPA) is currently seeking to validate technologies that can directly treat radioactively contaminated high mercury (Hg) subcategory wastes without removing the mercury from the waste. The Sulfur Polymer Stabilization/Solidification (SPSS) process developed at Brookhaven National Laboratory is one of several candidate technologies capable of successfully treating various Hg waste streams. To supplement previously supplied data on treatment of soils, EPA needs additional data concerning stabilization of high Hg subcategory waste sludges. To this end, a 5000 ppm sludge surrogate, containing approximately 50 wt% water, was successfully treated by pilot-scale SPSS processing. In two process runs, 85 and 95 wt% of water was recovered from the sludge during processing. At waste loadings of 30 wt% dry sludge, the treated waste form had no detectable mercury (<10 ppb) in TCLP leachates. Data gathered from the demonstration of treatment of this sludge will provide EPA with information to support revisions to current treatment requirements for high Hg subcategory wastes.

ADAMA, J.W.; BOWERMAN, B.S.; KALB, P.D.

2002-10-01T23:59:59.000Z

228

Surface characterization of Pd/Al2O3 sorbents for mercury capture from fuel gas  

SciTech Connect (OSTI)

The surface composition of a series of Pd/alumina sorbents has been characterized to better understand the factors influencing their ability to adsorb mercury from fuel gas. Both a temperature effect and a dispersion effect were found. Maximum adsorption of Hg occurred at the -lowest temperature tested, 204C, and decreased with increasing temperatures. Maximum adsorption of Hg on a per-atom basis of Pd is observed at low loadings of Pd ( < 8.5% Pd) due to better dispersion of Pd at those loadings; a change in its partitioning occurs at higher loadings. The presence of H2S 'in the fuel gas acts to promote the adsorption of Hg through its association with Hg in the Pd lattice.

Baltrus, J.P.; Granite, E.J.; Stanko, D.C.; Pennline, H.W.

2008-01-01T23:59:59.000Z

229

Surface characterization of Pd/Al2O3 sorbents for mercury capture from fuel gas  

SciTech Connect (OSTI)

The surface composition of a series of Pd/alumina sorbents has been characterized to better understand the factors influencing their ability to adsorb mercury from fuel gas. Both a temperature effect and a dispersion effect were found. Maximum adsorption of Hg occurred at the lowest temperature tested, 2048C, and decreased with increasing temperatures. Maximum adsorption of Hg on a per-atom basis of Pd is observed at low loadings of Pd (58.5% Pd) due to better dispersion of Pd at those loadings; a change in its partitioning occurs at higher loadings. The presence of H2S in the fuel gas acts to promote the adsorption of Hg through its association with Hg in the Pd lattice.

Baltrus, J.P.; Granite, E.J.; Stanko, D.C.; Pennline, H.W.

2008-09-01T23:59:59.000Z

230

Mercury Oxidation via Catalytic Barrier Filters Phase II  

SciTech Connect (OSTI)

In 2004, the Department of Energy National Energy Technology Laboratory awarded the University of North Dakota a Phase II University Coal Research grant to explore the feasibility of using barrier filters coated with a catalyst to oxidize elemental mercury in coal combustion flue gas streams. Oxidized mercury is substantially easier to remove than elemental mercury. If successful, this technique has the potential to substantially reduce mercury control costs for those installations that already utilize baghouse barrier filters for particulate removal. Completed in 2004, Phase I of this project successfully met its objectives of screening and assessing the possible feasibility of using catalyst coated barrier filters for the oxidation of vapor phase elemental mercury in coal combustion generated flue gas streams. Completed in September 2007, Phase II of this project successfully met its three objectives. First, an effective coating method for a catalytic barrier filter was found. Second, the effects of a simulated flue gas on the catalysts in a bench-scale reactor were determined. Finally, the performance of the best catalyst was assessed using real flue gas generated by a 19 kW research combustor firing each of three separate coal types.

Wayne Seames; Michael Mann; Darrin Muggli; Jason Hrdlicka; Carol Horabik

2007-09-30T23:59:59.000Z

231

HgTe-low-field Strained HgTe: a textbook 3D topological insulator  

E-Print Network [OSTI]

HgTe-low-field Strained HgTe: a textbook 3D topological insulator Clement Bouvier, Tristan Meunier martyrs 38054 Grenoble Cedex 9, France (Dated: December 9, 2011) Topological insulators can be seen-conductors and topological- insulators, other contributions make transport data more difficult to unravel. This letter

Paris-Sud XI, Universit de

232

Unexpected effects of gene deletion on mercury interactions with the methylation-deficient mutant hgcAB  

SciTech Connect (OSTI)

The hgcA and hgcB gene pair is essential for mercury (Hg) methylation by certain anaerobic bacteria,1 but little is known about how deletion of hgcAB affects cell surface interactions and intracellular uptake of Hg. Here, we compare hgcAB mutants with the wild-type (WT) strains of both Geobacter sulfurreducens PCA and Desulfovibrio desulfuricans ND132 and observe differences in Hg redox transformations, adsorption, and uptake in laboratory incubation studies. In both strains, deletion of hgcAB increased the reduction of Hg(II) but decreased the oxidation of Hg(0) under anaerobic conditions. The measured cellular thiol content in hgcAB mutants was lower than the WT, accounting for decreased adsorption and uptake of Hg. Despite the lack of methylation activity, Hg uptake by the hgcAB continued, albeit at a slower rate than the WT. These findings demonstrate that deletion of the hgcAB gene not only eliminates Hg methylation but also alters cell physiology, resulting in changes to Hg redox reactions, sorption, and uptake by cells.

Lin, Hui [ORNL] [ORNL; Hurt, Jr., Richard Ashley [ORNL; Johs, Alexander [ORNL] [ORNL; Parks, Jerry M [ORNL] [ORNL; Morrell-Falvey, Jennifer L [ORNL] [ORNL; Liang, Liyuan [ORNL] [ORNL; Elias, Dwayne A [ORNL] [ORNL; Gu, Baohua [ORNL] [ORNL

2014-01-01T23:59:59.000Z

233

Application of a Rule-Based Model to Estimate Mercury Exchange for Three Background Biomes in the Continental United States  

SciTech Connect (OSTI)

Ecosystems that have low mercury (Hg) concentrations (i.e., not enriched or impacted by geologic or anthropogenic processes) cover most of the terrestrial surface area of the earth yet their role as a net source or sink for atmospheric Hg is uncertain. Here we use empirical data to develop a rule-based model implemented within a geographic information system framework to estimate the spatial and temporal patterns of Hg flux for semiarid deserts, grasslands, and deciduous forests representing 45% of the continental United States. This exercise provides an indication of whether these ecosystems are a net source or sink for atmospheric Hg as well as a basis for recommendation of data to collect in future field sampling campaigns. Results indicated that soil alone was a small net source of atmospheric Hg and that emitted Hg could be accounted for based on Hg input by wet deposition. When foliar assimilation and wet deposition are added to the area estimate of soil Hg flux these biomes are a sink for atmospheric Hg.

Hartman, Jelena S. [University of Nevada, Reno; Weisberg, Peter J [University of Nevada, Reno; Pillai, Rekha [University of Nevada, Reno; Ericksen, Joey A. [University of Nevada, Reno; Gustin, Mae S. [University of Nevada, Reno; Kuiken, Todd [Tennessee Technological University; Zhang, Hong [Tennessee Technological University; Lindberg, Steven Eric [ORNL; Rytuba, J. J. [U.S. Geological Survey, Menlo Park, CA

2009-07-01T23:59:59.000Z

234

Mercury-Related Materials Studies  

E-Print Network [OSTI]

. Pawel, "Assessment of Cavitation-Erosion Resistance of Potential Pump Impeller Materials for Mercury of Cavitation Resistant Modifications to Type 316LN Stainless Steel in a Mercury Thermal Convection Loop," OakMercury-Related Materials Studies Van Graves IDS NF Ph M tiIDS-NF Phone Meeting Jan 26, 2010

McDonald, Kirk

235

Mercury-Related Materials Studies  

E-Print Network [OSTI]

Mercury-Related Materials Studies Van Graves IDS NF Ph M tiIDS-NF Phone Meeting Jan 26, 2010 #12 Evaluation of Cavitation Resistance of Type 316LN Stainless Steel in Mercury Using a Vibratory Horn," J. Nucl Pump Impeller Materials for Mercury Service at the Spallation Neutron Source," Oak Ridge National

McDonald, Kirk

236

Bioaccumulation of Mercury in Sharks  

E-Print Network [OSTI]

Bioaccumulation of Mercury in Sharks Part 2 a Using a subset of data collected on RJD shark research trips, you will analyze the mercury levels found in the Florida Sharks we catch. Based on your analysis, you will be able to conclude which species have the highest levels of mercury contamination

Miami, University of

237

Mercury Vapor At Long Valley Caldera Geothermal Area (Klusman...  

Open Energy Info (EERE)

Activity Date - 1979 Usefulness useful DOE-funding Unknown Exploration Basis A1-horizon soil samples collected in the vicinity of the resurgent dome and a known geothermal source...

238

Mercury Vapor At Haleakala Volcano Area (Thomas, 1986) | Open Energy  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data CenterFranconia, Virginia: Energy Resources Jump to:46 - 429Lacey,(MonasterLowellisMcDonald isMelletteEnclosed

239

Mercury Vapor At Kawaihae Area (Thomas, 1986) | Open Energy Information  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data CenterFranconia, Virginia: Energy Resources Jump to:46 - 429Lacey,(MonasterLowellisMcDonald isMelletteEnclosedInformation

240

Mercury Vapor At Lualualei Valley Area (Thomas, 1986) | Open Energy  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data CenterFranconia, Virginia: Energy Resources Jump to:46 - 429Lacey,(MonasterLowellisMcDonaldInformation Lahaina-Kaanapali Area1979)

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


241

Mercury Vapor At Medicine Lake Area (Kooten, 1987) | Open Energy  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data CenterFranconia, Virginia: Energy Resources Jump to:46 - 429Lacey,(MonasterLowellisMcDonaldInformation

242

Mercury Vapor At Mokapu Penninsula Area (Thomas, 1986) | Open Energy  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data CenterFranconia, Virginia: Energy Resources Jump to:46 - 429Lacey,(MonasterLowellisMcDonaldInformationEnergy Information Mickey

243

Mercury Vapor At Socorro Mountain Area (Kooten, 1987) | Open Energy  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data CenterFranconia, Virginia: Energy Resources Jump to:46 - 429Lacey,(MonasterLowellisMcDonaldInformationEnergyInformation Socorro

244

Water displacement mercury pump  

DOE Patents [OSTI]

A water displacement mercury pump has a fluid inlet conduit and diffuser, a valve, a pressure cannister, and a fluid outlet conduit. The valve has a valve head which seats in an opening in the cannister. The entire assembly is readily insertable into a process vessel which produces mercury as a product. As the mercury settles, it flows into the opening in the cannister displacing lighter material. When the valve is in a closed position, the pressure cannister is sealed except for the fluid inlet conduit and the fluid outlet conduit. Introduction of a lighter fluid into the cannister will act to displace a heavier fluid from the cannister via the fluid outlet conduit. The entire pump assembly penetrates only a top wall of the process vessel, and not the sides or the bottom wall of the process vessel. This insures a leak-proof environment and is especially suitable for processing of hazardous materials.

Nielsen, Marshall G. (Woodside, CA)

1985-01-01T23:59:59.000Z

245

Water displacement mercury pump  

DOE Patents [OSTI]

A water displacement mercury pump has a fluid inlet conduit and diffuser, a valve, a pressure cannister, and a fluid outlet conduit. The valve has a valve head which seats in an opening in the cannister. The entire assembly is readily insertable into a process vessel which produces mercury as a product. As the mercury settles, it flows into the opening in the cannister displacing lighter material. When the valve is in a closed position, the pressure cannister is sealed except for the fluid inlet conduit and the fluid outlet conduit. Introduction of a lighter fluid into the cannister will act to displace a heavier fluid from the cannister via the fluid outlet conduit. The entire pump assembly penetrates only a top wall of the process vessel, and not the sides or the bottom wall of the process vessel. This insures a leak-proof environment and is especially suitable for processing of hazardous materials.

Nielsen, M.G.

1984-04-20T23:59:59.000Z

246

Evaluation of Mercury Emissions from Coal-Fired Facilities with SCR and FGD Systems  

SciTech Connect (OSTI)

CONSOL Energy Inc., Research & Development (CONSOL), with support from the U.S. Department of Energy, National Energy Technology Laboratory (DOE) and the Electric Power Research Institute (EPRI), is evaluating the effects of selective catalytic reduction (SCR) on mercury (Hg) capture in coal-fired plants equipped with an electrostatic precipitator (ESP)--wet flue gas desulfurization (FGD) combination or a spray dyer absorber--fabric filter (SDA-FF) combination. In this program CONSOL is determining mercury speciation and removal at 10 coal-fired facilities. The principal purpose of this work is to develop a better understanding of the potential mercury removal ''co-benefits'' achieved by NO{sub x}, and SO{sub 2} control technologies. It is expected that these data will provide the basis for fundamental scientific insights into the nature of mercury chemistry in flue gas, the catalytic effect of SCR systems on mercury speciation and the efficacy of different FGD technologies for mercury capture. Ultimately, this insight could help to design and operate SCR and FGD systems to maximize mercury removal. The objectives are (1) to evaluate the effect of SCR on mercury capture in the ESP-FGD and SDA-FF combinations at coal-fired power plants, (2) evaluate the effect of SCR catalyst degradation on mercury capture; (3) evaluate the effect of low load operation on mercury capture in an SCR-FGD system, and (4) collect data that could provide the basis for fundamental scientific insights into the nature of mercury chemistry in flue gas, the catalytic effect of SCR systems on mercury speciation and the efficacy of different FGD technologies for mercury capture. This document, the ninth in a series of topical reports, describes the results and analysis of mercury sampling performed on Unit 1 at Plant 7, a 566 MW unit burning a bituminous coal containing 3.6% sulfur. The unit is equipped with a SCR, ESP, and wet FGD to control NO{sub x}, particulate, and SO{sub 2} emissions, respectively. Four sampling tests were performed in August 2004 during ozone season with the SCR operating; flue gas mercury speciation and concentrations were determined at the SCR inlet, SCR outlet, air heater outlet (ESP inlet), ESP outlet (FGD inlet), and at the stack (FGD outlet) using the Ontario Hydro method. Three sampling tests were also performed in November 2004 during non-ozone season with the SCR bypassed; flue gas mercury speciation and concentrations were determined at the ESP outlet (FGD inlet), and at the stack (FGD outlet). Process samples for material balances were collected during the flue gas measurements. The results show that, at the point where the flue gas enters the FGD, a greater percentage of the mercury was in the oxidized form when the SCR was operating compared to when the SCR was bypassed (97% vs 91%). This higher level of oxidation resulted in higher mercury removals in the FGD because the FGD removed 90-94% of the oxidized mercury in both cases. Total coal-to-stack mercury removal was 86% with the SCR operating, and 73% with the SCR bypassed. The average mercury mass balance closure was 81% during the ozone season tests and 87% during the non-ozone season tests.

J. A. Withum; S. C. Tseng; J. E. Locke

2006-01-31T23:59:59.000Z

247

Atmospheric Mercury near Salmon Falls Creek Reservoir in Southern Idaho  

SciTech Connect (OSTI)

Gaseous elemental mercury (GEM) and reactive gaseous mercury (RGM) were measured over two-week seasonal field campaigns near Salmon Falls Creek Reservoir in south-central Idaho from the summer of 2005 through the fall of 2006 and over the entire summer of 2006 using automated Tekran mercury analyzers. GEM, RGM, and particulate mercury (HgP) were also measured at a secondary site 90 km to the west in southwestern Idaho during the summer of 2006. The study was performed to characterize mercury air concentrations in the southern Idaho area for the first time, estimate mercury dry deposition rates, and investigate the source of observed elevated concentrations. High seasonal variability was observed with the highest GEM (1.91 0.9 ng m-3) and RGM (8.1 5.6 pg m-3) concentrations occurring in the summer and lower values in the winter (1.32 0.3 ng m-3, 3.2 2.9 pg m-3 for GEM, RGM respectively). The summer-average HgP concentrations were generally below detection limit (0.6 1 pg m-3). Seasonally-averaged deposition velocities calculated using a resistance model were 0.034 0.032, 0.043 0.040, 0.00084 0.0017 and 0.00036 0.0011 cm s-1 for GEM (spring, summer, fall, and winter, respectively) and 0.50 0.39, 0.40 0.31, 0.51 0.43 and 0.76 0.57 cm s-1 for RGM. The total annual RGM + GEM dry deposition estimate was calculated to be 11.9 3.3 g m-2, or about 2/3 of the total (wet + dry) deposition estimate for the area. Periodic elevated short-term GEM (2.2 12 ng m-3) and RGM (50 - 150 pg m-3) events were observed primarily during the warm seasons. Back-trajectory modeling and PSCF analysis indicated predominant source directions from the southeast (western Utah, northeastern Nevada) through the southwest (north-central Nevada) with fewer inputs from the northwest (southeastern Oregon and southwestern Idaho).

Michael L. Abbott; Jeffrey J. Einerson

2007-12-01T23:59:59.000Z

248

Analytical Methods for Measuring Mercury in Water, Sediment and Biota  

SciTech Connect (OSTI)

Mercury (Hg) exists in a large number of physical and chemical forms with a wide range of properties. Conversion between these different forms provides the basis for mercury's complex distribution pattern in local and global cycles and for its biological enrichment and effects. Since the 1960s, the growing awareness of environmental mercury pollution has stimulated the development of more accurate, precise and efficient methods of determining mercury and its compounds in a wide variety of matrices. During recent years new analytical techniques have become available that have contributed significantly to the understanding of mercury chemistry in natural systems. In particular, these include ultra sensitive and specific analytical equipment and contamination-free methodologies. These improvements allow for the determination of total mercury as well as major species of mercury to be made in water, sediments and soils, and biota. Analytical methods are selected depending on the nature of the sample, the concentration levels of mercury, and what species or fraction is to be quantified. The terms speciation and fractionation in analytical chemistry were addressed by the International Union for Pure and Applied Chemistry (IUPAC) which published guidelines (Templeton et al., 2000) or recommendations for the definition of speciation analysis. "Speciation analysis is the analytical activity of identifying and/or measuring the quantities of one or more individual chemical species in a sample. The chemical species are specific forms of an element defined as to isotopic composition, electronic or oxidation state, and/or complex or molecular structure. The speciation of an element is the distribution of an element amongst defined chemical species in a system. In case that it is not possible to determine the concentration of the different individual chemical species that sum up the total concentration of an element in a given matrix, meaning it is impossible to determine the speciation, it is a useful practice to do fractionation instead. Fractionation is the process of classification of an analyte or a group of analytes from a certain sample according to physical (e.g. size, solubility) or chemical (e.g. bonding, reactivity) properties."

Lasorsa, Brenda K.; Gill, Gary A.; Horvat, Milena

2012-06-07T23:59:59.000Z

249

Atmospheric Mercury Concentrations Near Salmon Falls Creek Reservoir - Phase 1  

SciTech Connect (OSTI)

Elemental and reactive gaseous mercury (EGM/RGM) were measured in ambient air concentrations over a two-week period in July/August 2005 near Salmon Falls Creek Reservoir, a popular fishery located 50 km southwest of Twin Falls, Idaho. A fish consumption advisory for mercury was posted at the reservoir in 2002 by the Idaho Department of Health and Welfare. The air measurements were part of a multi-media (water, sediment, precipitation, air) study initiated by the Idaho Department of Environmental Quality and the U.S. Environmental Protection Agency (EPA) Region 10 to identify potential sources of mercury contamination to the reservoir. The sampling site is located about 150 km northeast of large gold mining operations in Nevada, which are known to emit large amounts of mercury to the atmosphere (est. 2,200 kg/y from EPA 2003 Toxic Release Inventory). The work was co-funded by the Idaho National Laboratorys Community Assistance Program and has a secondary objective to better understand mercury inputs to the environment near the INL, which lies approximately 230 km to the northeast. Sampling results showed that both EGM and RGM concentrations were significantly elevated (~ 30 70%, P<0.05) compared to known regional background concentrations. Elevated short-term RGM concentrations (the primary form that deposits) were likely due to atmospheric oxidation of high EGM concentrations, which suggests that EGM loading from upwind sources could increase Hg deposition in the area. Back-trajectory analyses indicated that elevated EGM and RGM occurred when air parcels came out of north-central and northeastern Nevada. One EGM peak occurred when the air parcels came out of northwestern Utah. Background concentrations occurred when the air was from upwind locations in Idaho (both northwest and northeast). Based on 2003 EPA Toxic Release Inventory data, it is likely that most of the observed peaks were from Nevada gold mine sources. Emissions from known large natural mercury sources in that area cannot account for the observed EGM peaks due to their diffuse source geometry and the large (170 km) transport distance involved. The EGM peak originating from northwestern Utah air may be from three known mercury sources west of Salt Lake City (Kennecott, US Magnesium, Clean Harbors Aragonite) and/or the 1600 MW coal-fired Intermountain Power plant near Delta. However, the relative importance of these short-term peaks for long-term watershed mercury loading (critical factor affecting fish concentrations) is not known, and there is a need to better quantify the annual frequency and magnitude of these different inputs over a longer period of time.

M. L. Abbott

2005-10-01T23:59:59.000Z

250

Environmental Sampling FY03 Annual Report - Understanding the Movement of Mercury on the INEEL  

SciTech Connect (OSTI)

Environmental mercury measurements were started in Fy-01 at the Idaho National Engineering Laboratory (INEEL) to monitor downwind impacts from on-going waste treatment operations at the Idaho Nuclear Technology and Engineering Center (INTEC) and to improve our scientific understanding of mercury fate and transport in this region. This document provides a summary of the sampling done in FY04. Continuous total gaseous mercury (TGM) measurements were made using a Tekran Model 2537A mercury vapor analyzer during October 2002 and from February through July 2003. The equipment was deployed in a self-contained field trailer at the Experimental Field Station (EFS) four kilometers downwind (northeast) of INTEC. Mercury surface-to-air flux measurements were made in October 2002 and from February through May 2003 to better understand the fate of the estimated 1500 kg of mercury emitted from 36 years of calciner operations at INTEC and to improve our scientific understanding of mercury environmental cycling in this region. Flux was measured using an INEEL-designed dynamic flux chamber system with a Tekran automated dual sampling (TADS) unit. Diel flux was positively correlated with solar radiation (r = 0.65), air temperature (r = 0.64), and wind speed (r = 0.38), and a general linear model for flux prediction at the INEEL was developed. Reactive gaseous mercury (RGM) was measured at EFS in July using a Tekran Model 1130 mercury speciation unit. Based on comparisons with other published data around the U.S., mercury air concentrations and surface flux rates directly downwind from INTEC were not distinguishable from remote area (non-industrial) background levels during the monitoring period.

Michael L. Abbott

2003-10-01T23:59:59.000Z

251

Mechanism of terahertz photoconductivity in semimetallic HgTe/CdHgTe quantum wells  

SciTech Connect (OSTI)

Terahertz photoconductivity in magnetic fields in semimetallic HgTe/CdHgTe quantum wells has been studied. The main contribution to photoconductivity comes from a signal that appears as a result of electron-gas heating. It is shown that, with the cyclotron resonance conditions satisfied, the photoconductivity signal is composed of cyclotron-resonance and bolometric components. However, in this case too, the bolometric contribution predominates.

Vasilyev, Yu. B., E-mail: yu.vasilyev@mail.ioffe.ru [Russian Academy of Sciences, Ioffe Physical-Technical Institute (Russian Federation); Mikhailov, N. N. [Russian Academy of Sciences, Rzhanov Institute of Semiconductor Physics, Siberian Branch (Russian Federation); Gouider, F. [Institut fuer Angewandte Physik (Germany); Vasilyeva, G. Yu. [St. Petersburg State Polytechnic University (Russian Federation); Nachtwei, G. [Institut fuer Angewandte Physik (Germany)

2012-05-15T23:59:59.000Z

252

Mercury Information Clearinghouse  

SciTech Connect (OSTI)

The Canadian Electricity Association (CEA) identified a need and contracted the Energy & Environmental Research Center (EERC) to create and maintain an information clearinghouse on global research and development activities related to mercury emissions from coal-fired electric utilities. With the support of CEA, the Center for Air Toxic Metals{reg_sign} (CATM{reg_sign}) Affiliates, and the U.S. Department of Energy (DOE), the EERC developed comprehensive quarterly information updates that provide a detailed assessment of developments in the various areas of mercury monitoring, control, policy, and research. A total of eight topical reports were completed and are summarized and updated in this final CEA quarterly report. The original quarterly reports can be viewed at the CEA Web site (www.ceamercuryprogram.ca). In addition to a comprehensive update of previous mercury-related topics, a review of results from the CEA Mercury Program is provided. Members of Canada's coal-fired electricity generation sector (ATCO Power, EPCOR, Manitoba Hydro, New Brunswick Power, Nova Scotia Power Inc., Ontario Power Generation, SaskPower, and TransAlta) and CEA, have compiled an extensive database of information from stack-, coal-, and ash-sampling activities. Data from this effort are also available at the CEA Web site and have provided critical information for establishing and reviewing a mercury standard for Canada that is protective of environment and public health and is cost-effective. Specific goals outlined for the CEA mercury program included the following: (1) Improve emission inventories and develop management options through an intensive 2-year coal-, ash-, and stack-sampling program; (2) Promote effective stack testing through the development of guidance material and the support of on-site training on the Ontario Hydro method for employees, government representatives, and contractors on an as-needed basis; (3) Strengthen laboratory analytical capabilities through analysis and quality assurance programs; and (4) Create and maintain an information clearinghouse to ensure that all parties can keep informed on global mercury research and development activities.

Chad A. Wocken; Michael J. Holmes; Dennis L. Laudal; Debra F. Pflughoeft-Hassett; Greg F. Weber; Nicholas V. C. Ralston; Stanley J. Miller; Grant E. Dunham; Edwin S. Olson; Laura J. Raymond; John H. Pavlish; Everett A. Sondreal; Steven A. Benson

2006-03-31T23:59:59.000Z

253

Method and apparatus for monitoring the flow of mercury in a system  

DOE Patents [OSTI]

An apparatus and method for monitoring the flow of mercury in a system. The equipment enables the entrainment of the mercury in a carrier gas e.g., an inert gas, which passes as mercury vapor between a pair of optically transparent windows. The attenuation of the emission is indicative of the quantity of mercury (and its isotopes) in the system. A 253.7 nm light is shone through one of the windows and the unabsorbed light is detected through the other window. The absorption of the 253.7 nm light is thereby measured whereby the quantity of mercury passing between the windows can be determined. The apparatus includes an in-line sensor for measuring the quantity of mercury. It includes a conduit together with a pair of apertures disposed in a face to face relationship and arranged on opposite sides of the conduit. A pair of optically transparent windows are disposed upon a pair of viewing tubes. A portion of each of the tubes is disposed inside of the conduit and within each of the apertures. The two windows are disposed in a face to face relationship on the ends of the viewing tubes and the entire assembly is hermetically sealed from the atmosphere whereby when 253.7 nm ultraviolet light is shone through one of the windows and detected through the other, the quantity of mercury which is passing by can be continuously monitored due to absorption which is indicated by attenuation of the amplitude of the observed emission.

Grossman, Mark W. (Belmont, MA)

1987-01-01T23:59:59.000Z

254

Development Of Chemical Reduction And Air Stripping Processes To Remove Mercury From Wastewater  

SciTech Connect (OSTI)

This study evaluates the removal of mercury from wastewater using chemical reduction and air stripping using a full-scale treatment system at the Savannah River Site. The existing water treatment system utilizes air stripping as the unit operation to remove organic compounds from groundwater that also contains mercury (C ~ 250 ng/L). The baseline air stripping process was ineffective in removing mercury and the water exceeded a proposed limit of 51 ng/L. To test an enhancement to the existing treatment modality a continuous dose of reducing agent was injected for 6-hours at the inlet of the air stripper. This action resulted in the chemical reduction of mercury to Hg(0), a species that is removable with the existing unit operation. During the injection period a 94% decrease in concentration was observed and the effluent satisfied proposed limits. The process was optimized over a 2-day period by sequentially evaluating dose rates ranging from 0.64X to 297X stoichiometry. A minimum dose of 16X stoichiometry was necessary to initiate the reduction reaction that facilitated the mercury removal. Competing electron acceptors likely inhibited the reaction at the lower 1 doses, which prevented removal by air stripping. These results indicate that chemical reduction coupled with air stripping can effectively treat large-volumes of water to emerging part per trillion regulatory standards for mercury.

Jackson, Dennis G.; Looney, Brian B.; Craig, Robert R.; Thompson, Martha C.; Kmetz, Thomas F.

2013-07-10T23:59:59.000Z

255

Achieving very low mercury levels in refinery wastewater by membrane filtration.  

SciTech Connect (OSTI)

Microfiltration (MF), ultrafiltration (UF), nanofiltration (NF) and reverse osmosis (RO) membranes were evaluated for their ability to achieve the world's most stringent Hg discharge criterion (<1.3 ng/L) in an oil refinery's wastewater. The membrane processes were operated at three different pressures to demonstrate the potential for each membrane technology to achieve the targeted effluent mercury concentrations. The presence of mercury in the particulate form in the refinery wastewater makes the use of MF and UF membrane technologies more attractive in achieving very low mercury levels in the treated wastewater. Both NF and RO were also able to meet the target mercury concentration at lower operating pressures (20.7 bar). However, higher operating pressures ({ge}34.5 bar) had a significant effect on NF and RO flux and fouling rates, as well as on permeate quality. SEM images of the membranes showed that pore blockage and narrowing were the dominant fouling mechanisms for the MF membrane while surface coverage was the dominant fouling mechanism for the other membranes. The correlation between mercury concentration and particle size distribution was also investigated to understand mercury removal mechanisms by membrane filtration. The mean particle diameter decreased with filtration from 1.1 {+-} 0.0 {micro}m to 0.74 {+-} 0.2 {micro}m after UF.

Urgun Demirtas, M.; Benda, P.; Gillenwater, P. S.; Negri, M. C.; Xiong, H.; Snyder, S. W. (Center for Nanoscale Materials); ( ES)

2012-05-15T23:59:59.000Z

256

Vapor spill monitoring method  

DOE Patents [OSTI]

Method for continuous sampling of liquified natural gas effluent from a spill pipe, vaporizing the cold liquified natural gas, and feeding the vaporized gas into an infrared detector to measure the gas composition. The apparatus utilizes a probe having an inner channel for receiving samples of liquified natural gas and a surrounding water jacket through which warm water is flowed to flash vaporize the liquified natural gas.

Bianchini, Gregory M. (Livermore, CA); McRae, Thomas G. (Livermore, CA)

1985-01-01T23:59:59.000Z

257

Mercury control in 2009  

SciTech Connect (OSTI)

Although activated carbon injection (ACI) has been proven to be effective for many configurations and is a preferred option at many plants sufficient quantities of powdered activated coking (PAC) must be available to meet future needs. The authors estimate that upcoming federal and state regulations will result in tripling the annual US demand for activated carbon to nearly 1.5 billion lb from approximately 450 million lb. Rapid expansion of US production capacity is required. Many PAC manufacturers are discussing expansion of their existing production capabilities. One company, ADA Carbon Solutions, is in the process of constructing the largest activated carbon facility in North America to meet the future demand for PAC as a sorbent for mercury control. Emission control technology development and commercialization is driven by regulation and legislation. Although ACI will not achieve > 90% mercury control at every plant, the expected required MACT legislation level, it offers promise as a low-cost primary mercury control technology option for many configurations and an important trim technology for others. ACI has emerged as the clear mercury-specific control option of choice, representing over 98% of the commercial mercury control system orders to date. As state regulations are implemented and the potential for a federal rule becomes more imminent, suppliers are continuing to develop technologies to improve the cost effectiveness and limit the balance of plant impacts associated with ACI and are developing additional PAC production capabilities to ensure that the industry's needs are met. The commercialisation of ACI is a clear example of industry, through the dedication of many individuals and companies with support from the DOE and EPRI, meeting the challenge of developing cost-effectively reducing emissions from coal-fired power plants. 7 refs., 1 fig.

Sjostrom, S.; Durham, M.; Bustard, J.; Martin, C. [ADA Environmental Solutions, Littleton, CO (United States)

2009-07-15T23:59:59.000Z

258

Evaluation of Mercury Emissions from Coal-Fired Facilities with SCR and FGD Systems  

SciTech Connect (OSTI)

CONSOL Energy Inc., Research & Development (CONSOL), with support from the U.S. Department of Energy, National Energy Technology Laboratory (DOE) and the Electric Power Research Institute (EPRI), is evaluating the effects of selective catalytic reduction (SCR) on mercury (Hg) capture in coal-fired plants equipped with an electrostatic precipitator (ESP)--wet flue gas desulfurization (FGD) combination or a spray dyer absorber--fabric filter (SDA-FF) combination. In this program CONSOL is determining mercury speciation and removal at 10 coal-fired facilities. The principal purpose of this work is to develop a better understanding of the potential mercury removal ''co-benefits'' achieved by NO{sub x}, and SO{sub 2} control technologies. It is expected that this data will provide the basis for fundamental scientific insights into the nature of mercury chemistry in flue gas, the catalytic effect of SCR systems on mercury speciation and the efficacy of different FGD technologies for mercury capture. Ultimately, this insight could help to design and operate SCR and FGD systems to maximize mercury removal. The objectives are (1) to evaluate the effect of SCR on mercury capture in the ESP-FGD and SDA-FF combinations at coal-fired power plants, (2) evaluate the effect of SCR catalyst degradation on mercury capture; (3) evaluate the effect of low load operation on mercury capture in an SCR-FGD system, and (4) collect data that could provide the basis for fundamental scientific insights into the nature of mercury chemistry in flue gas, the catalytic effect of SCR systems on mercury speciation and the efficacy of different FGD technologies for mercury capture. This document, the tenth in a series of topical reports, describes the results and analysis of mercury sampling performed on two 468 MW units burning bituminous coal containing 1.3-1.7% sulfur. Unit 2 is equipped with an SCR, ESP, and wet FGD to control NO{sub x}, particulate, and SO{sub 2} emissions, respectively. Unit 1 is similar to Unit 2, except that Unit 1 has no SCR for NOx control. Four sampling tests were performed on both units in January 2005; flue gas mercury speciation and concentrations were determined at the economizer outlet, air heater outlet (ESP inlet), ESP outlet (FGD inlet), and at the stack (FGD outlet) using the Ontario Hydro method. Process samples for material balances were collected with the flue gas measurements. The results show that the SCR increased the oxidation of the mercury at the air heater outlet. At the exit of the air heater, a greater percentage of the mercury was in the oxidized and particulate forms on the unit equipped with an SCR compared to the unit without an SCR (97.4% vs 91%). This higher level of oxidation resulted in higher mercury removals in the scrubber. Total mercury removal averaged 97% on the unit with the SCR, and 87% on the unit without the SCR. The average mercury mass balance closure was 84% on Unit 1 and 103% on Unit 2.

J. A. Withum; J. E. Locke

2006-02-01T23:59:59.000Z

259

Effects of reservoir drawdown and refill on mercury levels in fish and other biota  

SciTech Connect (OSTI)

Mercury bioavailability from contaminated sediments is controlled by methylation, related to bacterial activity and degradable organic material. These variables may be affected by large changes in water level and chemistry in a reservoir. At Par Pond, a 1,200 ha impoundment on the USDOE Savannah River Site, South Carolina, potential failure of an earthen dam prompted lowering the reservoir by 3 meters over a two month period in 1991, decreasing water volume about 70%. The reservoir was refilled over a two month period in 1995. Largemouth bass (Micropterus salmoides) were sampled at quarterly intervals before, during and after the drawdown. Length and weight were determined, and liver and muscle analyzed for total Hg. Hg was also measured in top level predators (alligators), forage fish, macrophytes and invertebrates. From Fall 1991 Winter 1994--5, Hg ranged from 0.05 to 2.0 ug/g wet mass in bass muscle, and was strongly related to fish size, based on about 400 fish. Condition factor rose soon after drawdown, then declined as forage populations collapsed. Using fish size as covariate, bass muscle Hg was greater in spring 1992 than all other sampling dates. However, after 3 years of drawdown, there was no overall trend in bass Hg. Forage species differed in Hg, with highest concentrations in brook silversides (0.13 {micro}g Hg/g wet mass in 2 g fish). Alligators contained up to 20 {micro}g Hg/g dry mass in liver. Refill caused inundation of terrestrial plants on exposed sediments, and microbial action associated with the decay of these may enhance Hg methylation. Experiments with caged fish are underway to measure uptake rates.

Jagoe, C.H.; Salice, C.; Yabnochko, G.; Grasman, B.T.; Youngblood, T. [Savannah River Ecology Lab., Aiken, SC (United States)

1995-12-31T23:59:59.000Z

260

Biosequence Similarity Search on the Mercury System  

E-Print Network [OSTI]

Biosequence Similarity Search on the Mercury System Praveen Krishnamurthy, Jeremy Buhler, Roger Chamberlain, Mark Franklin, Kwame Gyang, and Joseph Lancaster, "Biosequence Similarity Search on the Mercury on the Mercury System Praveen Krishnamurthy, Jeremy Buhler, Roger Chamberlain, Mark Franklin, Kwame Gyang

Chamberlain, Roger

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


261

Recovery of mercury from acid waste residues  

DOE Patents [OSTI]

Mercury can be recovered from nitric acid-containing fluids by reacting the fluid with aluminum metal to produce mercury metal, and thence quenching the reactivity of the nitric acid prior to nitration of the mercury metal. 1 fig.

Greenhalgh, W.O.

1987-02-27T23:59:59.000Z

262

Recovery of mercury from acid waste residues  

DOE Patents [OSTI]

Mercury can be recovered from nitric acid-containing fluids by reacting the fluid with aluminum metal to produce mercury metal, and then quenching the reactivity of the nitric acid prior to nitration of the mercury metal.

Greenhalgh, Wilbur O. (Richland, WA)

1989-01-01T23:59:59.000Z

263

INTERIM RESULTS FROM A STUDY OF THE IMPACTS OF TIN(II) BASED MERCURY TREATMENT IN A SMALL STREAM ECOSYSTEM: TIMS BRANCH, SAVANNAH RIVER SITE  

SciTech Connect (OSTI)

Mercury (Hg) has been identified as a 'persistent, bioaccumulative and toxic' pollutant with widespread impacts throughout North America and the world (EPA. 1997a, 1997b, 1998a, 1998b, 2000). Although most of the mercury in the environment is inorganic Hg, a small proportion of total Hg is transformed through the actions of aquatic microbes into methylmercury (MeHg). In contrast to virtually all other metals, MeHg biomagnifies or becomes increasingly concentrated as it is transferred through aquatic food chains so that the consumption of mercury contaminated fish is the primary route of this toxin to humans. For this reason, the ambient water quality criterion (AWQC) for mercury is based on a fish tissue endpoint rather than an aqueous Hg concentration, as the tissue concentration (e.g., < 0.3 {mu}g/g fillet) is considered to be a more consistent indicator of exposure and risk (EPA, 2001). Effective mercury remediation at point-source contaminated sites requires an understanding of the nature and magnitude of mercury inputs, and also knowledge of how these inputs must be controlled in order to achieve the desired reduction of mercury contamination in biota necessary for compliance with AWQC targets. One of the challenges to remediation is that mercury body burdens in fish are more closely linked to aqueous MeHg than to inorganic Hg concentrations (Sveinsdottir and Mason 2005), but MeHg production is not easily predicted or controlled. At point-source contaminated sites, mercury methylation is not only affected by the absolute mercury load, but also by the form of mercury loaded. In addition, once MeHg is formed, the hydrology, trophic structure, and water chemistry of a given system affect how it is transformed and transferred through the food chain to fish. Decreasing inorganic Hg concentrations and loading may often therefore be a more achievable remediation goal, but has led to mixed results in terms of responses in fish bioaccumulation. A number of source control measures have resulted in rapid responses in lake or reservoir fisheries (Joslin 1994, Turner and Southworth 1999; Orihel et al., 2007), but examples of similar responses in Hg-contaminated stream ecosystems are less common. Recent work suggests that stream systems may actually be more susceptible to mercury bioaccumulation than lakes, highlighting the need to better understand the ecological drivers of mercury bioaccumulation in stream-dwelling fish (Chasar et al. 2009, Ward et al. 2010). In the present study we examine the response of fish to remedial actions in Tims Branch, a point-source contaminated stream on the Department of Energy's (DOE) Savannah River Site in Aiken, South Carolina. This second order stream received inorganic mercury inputs at its headwaters from the 1950s-2000s which contaminated the water, sediments, and biota downstream. In 2007, an innovative mercury removal system using tin (II) chloride (stannous chloride, SnCl{sub 2}) was implemented at a pre-existing air stripper. Tin(II) reduces dissolved Hg (II) to Hg (0), which is removed by the air stripper. During this process, tin(II) is oxidized to tin (IV) which is expected to precipitate as colloidal tin(IV) oxides and hydroxides, particulate materials with relatively low toxicity (Hallas and Cooney, 1981, EPA 2002, ATSDR, 2005). The objectives of the present research are to provide an initial assessment of the net impacts of the tin(II) based mercury treatment on key biota and to document the distribution and fate of inorganic tin in this small stream ecosystem after the first several years of operating a full scale system. To support these objectives, we collected fish, sediment, water, invertebrates, and biofilm samples from Tims Branch to quantify the general behavior and accumulation patterns for mercury and tin in the ecosystem and to determine if the treatment process has resulted in: (1) a measurable beneficial impact on (i.e., decrease of) mercury concentration in upper trophic level fish and other biota; this is a key environmental endpoint since reducing mercury concen

Looney, B.; Bryan, L.; Mathews, T.

2012-03-30T23:59:59.000Z

264

Dipole Bands in {sup 196}Hg  

SciTech Connect (OSTI)

High spin states in {sup 196}Hg have been populated in the {sup 198}Pt({alpha},6n) reaction at 65 MeV and the level scheme has been extended. A new dipole band has been observed and a previously observed dipole has been confirmed. Excitation energies, spins and parities of these bands were determined from DCO ratio and linear polarization measurements. Possible quasiparticle excitations responsible for these structures are discussed.

Lawrie, J. J.; Lawrie, E. A.; Newman, R. T.; Sharpey-Schafer, J. F.; Smit, F. D. [iThemba LABS, PO Box 722, Somerset West 7129 (South Africa); Msezane, B. [iThemba LABS, PO Box 722, Somerset West 7129 (South Africa); Physics Department, University of Zululand, Private Bag X1001, Kwadlangezwa 3886 (South Africa); Benatar, M.; Mabala, G. K.; Mutshena, K. P. [iThemba LABS, PO Box 722, Somerset West 7129 (South Africa); Physics Department, University of Cape Town, Rondebosch 7700 (South Africa); Federke, M.; Mullins, S. M. [Physics Department, University of Cape Town, Rondebosch 7700 (South Africa); Ncapayi, N. J.; Vymers, P. [iThemba LABS, PO Box 722, Somerset West 7129 (South Africa); Physics Department, University of the Western Cape, Private Bag X17, Belleville 7535 (South Africa)

2011-10-28T23:59:59.000Z

265

Innovative Mercury Treatment Benefits Stream, Fish | Department...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Mercury Treatment Benefits Stream, Fish Innovative Mercury Treatment Benefits Stream, Fish October 1, 2012 - 12:00pm Addthis Oak Ridge scientists Kelly Roy, left, and Trent Jett...

266

Neutrino Factory Mercury Flow Loop  

E-Print Network [OSTI]

Neutrino Factory Mercury Flow Loop V. GravesV. Graves C. Caldwell IDS-NF Videoconference March 9, 2010 #12;Flow Loop Review · 1 cm dia nozzle, 20 m/s jet requires 1.57 liter/sec mercury flow (94 2 liter/min 24 9 gpm)mercury flow (94.2 liter/min, 24.9 gpm). · MERIT experiment showed that a pump

McDonald, Kirk

267

An assessment of mercury emissions and health risks from a coal-fired power plant  

SciTech Connect (OSTI)

Title 3 of the 1990 Clean Air Act Amendments (CAAA) mandated that the US Environmental Protection Agency (EPA) evaluate the need to regulate mercury emissions from electric utilities. In support of this forthcoming regulatory analysis the U.S. DOE, sponsored a risk assessment project at Brookhaven (BNL) to evaluate methylmercury (MeHg) hazards independently. In the US MeHg is the predominant way of exposure to mercury originated in the atmosphere. In the BNL study, health risks to adults resulting from Hg emissions from a hypothetical 1,000 MW coal-fired power plant were estimated using probabilistic risk assessment techniques. This study showed that the effects of emissions of a single power plant may double the background exposures to MeHg resulting from consuming fish obtained from a localized area near the power plant. Even at these more elevated exposure levels, the attributable incidence in mild neurological symptoms was estimated to be quite small, especially when compared with the estimated background incidence in the population. The current paper summarizes the basic conclusions of this assessment and highlights issues dealing with emissions control and environmental transport.

Fthenakis, V.M.; Lipfert, F.; Moskowitz, P. [Brookhaven National Lab., Upton, NY (United States). Analytical Sciences Div.

1994-12-01T23:59:59.000Z

268

Abundance analysis of SB2 binary stars with HgMn primaries  

E-Print Network [OSTI]

We present a short review of the abundances in the atmospheres of SB2 systems with Mercury-Manganese (HgMn) primaries. Up to now a careful study has been made for both components of 8 out of 17 known SB2 binaries with orbital periods shorter than 100 days and mass ratio ranging from 1.08 to 2.2. For all eight systems we observe a lower Mn abundance in the secondary's atmospheres than in the primary's. Significant difference in the abundances is also found for some peculiar elements such as Ga, Xe, Pt. All secondary stars with effective temperatures less than 10000 K show abundance characteristics typical of the metallic-line stars.

T. Ryabchikova

1998-05-06T23:59:59.000Z

269

Method for scavenging mercury  

DOE Patents [OSTI]

Disclosed herein is a method for removing mercury from a gas stream comprising contacting the gas stream with a getter composition comprising bromine, bromochloride, sulphur bromide, sulphur dichloride or sulphur monochloride and mixtures thereof. In one preferred embodiment the getter composition is adsorbed onto a sorbent. The sorbent may be selected from the group consisting of flyash, limestone, lime, calcium sulphate, calcium sulfite, activated carbon, charcoal, silicate, alumina and mixtures thereof. Preferred is flyash, activated carbon and silica.

Chang, Shih-ger (El Cerrito, CA); Liu, Shou-heng (Kaohsiung, TW); Liu, Zhao-rong (Beijing, CN); Yan, Naiqiang (Berkeley, CA)

2009-01-20T23:59:59.000Z

270

Method for scavenging mercury  

DOE Patents [OSTI]

Disclosed herein is a method for removing mercury from a gas stream comprising contacting the gas stream with a getter composition comprising bromine, bromochloride, sulphur bromide, sulphur dichloride or sulphur monochloride and mixtures thereof. In one preferred embodiment the getter composition is adsorbed onto a sorbent. The sorbent may be selected from the group consisting of flyash, limestone, lime, calcium sulphate, calcium sulfite, activated carbon, charcoal, silicate, alumina and mixtures thereof. Preferred is flyash, activated carbon and silica.

Chang, Shih-Ger (El Cerrito, CA); Liu, Shou-Heng (Kaohsiung, TW); Liu, Zhao-Rong (Beijing, CN); Yan, Naiqiang (Berkeley, CA)

2011-08-30T23:59:59.000Z

271

Method for scavenging mercury  

DOE Patents [OSTI]

Disclosed herein is a method for removing mercury from a gas stream comprising contacting the gas stream with a getter composition comprising bromine, bromochloride, sulphur bromide, sulphur dichloride or sulphur monochloride and mixtures thereof. In one preferred embodiment the getter composition is adsorbed onto a sorbent. The sorbent may be selected from the group consisting flyash, limestone, lime, calcium sulphate, calcium sulfite, activated carbon, charcoal, silicate, alumina and mixtures thereof. Preferred is flyash, activated carbon and silica.

Chang, Shih-ger (El Cerrito, CA); Liu, Shou-heng (Kaohsiung, TW); Liu, Zhao-rong (Bejing, CN); Yan, Naiqiang (Burkeley, CA)

2010-07-13T23:59:59.000Z

272

Microbial pathways for the mobilization of mercury as Hg(O) in anoxic subsurface environments  

SciTech Connect (OSTI)

The goal of our project which was initiated in June 2005 is focused on the presence of merA in microbial communities of anoxic environments and the effect of anaerobic respiratory pathways on MR expression and activities. The following progress has been made to date: PCR primers were designed to span the known phylogenetic range of merA genes of Gram-negative bacteria. In control experiments, these primers successfully amplified a 288 bp region at the 3? end of previously characterized merA genes from Shewanella putrefaciens pMERPH, Acidithiobacillus ferrooxidans, Pseudomonas stutzeri pPB, Tn5041, Pseudomonas sp. K-62, and Serratia marcescens pDU1358.

Barkay, Tamar

2005-06-01T23:59:59.000Z

273

Technology demonstration for reducing mercury emissions from small-scale gold refining facilities.  

SciTech Connect (OSTI)

Gold that is brought from artisanal and small-scale gold mining areas to gold shops for processing and sale typically contains 5-40% mercury. The uncontrolled removal of the residual mercury in gold shops by using high-temperature evaporation can be a significant source of mercury emissions in urban areas where the shops are located. Emissions from gold shop hoods during a burn can exceed 1,000 mg/m{sup 3}. Because the saturation concentration of mercury vapor at operating temperatures at the hood exhaust is less than 100 mg/m{sup 3}, the dominant component of the exhaust is in the form of aerosol or liquid particles. The U.S. Environmental Protection Agency (EPA), with technical support from Argonne National Laboratory (Argonne), has completed a project to design and test a technology to remove the dominant aerosol component in the emissions from gold shops. The objective was to demonstrate a technology that could be manufactured at low cost and by using locally available materials and manufacturing capabilities. Six prototypes designed by Argonne were locally manufactured, installed, and tested in gold shops in Itaituba and Creporizao, Brazil. The initial prototype design incorporated a pebble bed as the media for collecting the mercury aerosols, and a mercury collection efficiency of over 90% was demonstrated. Though achieving high efficiencies, the initial prototype was determined to have practical disadvantages such as excessive weight, a somewhat complex construction, and high costs (>US$1,000). To further simplify the construction, operation, and associated costs, a second prototype design was developed in which the pebble bed was replaced with slotted steel baffle plates. The system was designed to have flexibility for installation in various hood configurations. The second prototype with the baffle plate design was installed and tested in several different hood/exhaust systems to determine the optimal installation configuration. The significance of coagulation and collection of the mercury aerosols in exhaust ducts, which is dependent on the hood and collector configuration, was also evaluated. Prototype demonstration tests verified the theoretical basis for mercury aerosol capture that can be used to optimize the baffle plate design, flow rates, and hood exhaust ducts and plenum to achieve 80% or higher removal efficiencies. Results indicated that installation configuration significantly influences a system's capture efficiency. Configurations that retained existing inlet ducts resulted in system efficiencies of more than 80%, whereas installation configurations without inlet ducts significantly reduced capture efficiency. As an alternative to increasing the volume of inlet ducts, the number of baffle plates in the system baffle assembly could be doubled to increase efficiency. Recommended installation and operation procedures were developed on the basis of these results. A water-based mercury capture system developed in Indonesia for installation in smaller shops was also tested and shown to be effective for certain applications. The cost of construction and installation of the baffle plate prototype was approximately US$400. These costs were reported as acceptable by local gold shop owners and government regulators, and were significantly lower than the cost of an alternate charcoal/copper mesh mercury filter available in the region, which costs about US$10,000. A sampling procedure that consists of a particle filter combined with a vapor analyzer was demonstrated as an effective procedure for analyzing both the aerosol and vapor components of the mercury concentrations. Two key findings for enhancing higher mercury collection were identified. First, the aerosol/vapor mercury emissions must be given sufficient time for the mercury particles to coagulate to a size that can be readily captured by the baffle plates. An interval of at least 6 seconds of transit time between the point of evaporation and contact with the slotted baffle plates is recommended. Some particles will also deposit in the exhaust ducts

Habegger, L. J.; Fernandez, L. E.; Engle, M.; Bailey, J. L.; Peterson, D. P.; MacDonell, M. M.; U.S. Environmental Protection Agency

2008-06-30T23:59:59.000Z

274

Investigation and Demonstration of Dry Carbon-Based Sorbent Injection for Mercury Control  

SciTech Connect (OSTI)

Public Service Company of Colorado and ADA Technologies, Inc. have performed a study of the injection of activated carbon for the removal of vapor-phase mercury from coal-fired flue gas streams. The project was completed under contract to the US Department of Energy's National Energy Technology Laboratory, with contributions from EPRI and Public Service Company. The prime contractor for the project was Public Service Company, with ADA Technologies as the major subcontractor providing technical support to all aspects of the project. The research and development effort was conducted in two phases. In Phase I a pilot facility was fabricated and tests were performed using dry carbon-based sorbent injection for mercury control on a coal-fired flue gas slipstream extracted from an operating power plant. Phase II was designed to move carbon injection technology towards commercial application on coal-fired power plants by addressing key reliability and operability concerns. Phase II field work included further development work with the Phase I pilot and mercury measurements on several of PSCo's coal-fired generating units. In addition, tests were run on collected sorbent plus fly ash to evaluate the impact of the activated carbon sorbent on the disposal of fly ash. An economic analysis was performed where pilot plant test data was used to develop a model to predict estimated costs of mercury removal from plants burning western coals. Testing in the pilot plant was undertaken to quantify the effects of plant configuration, flue gas temperature, and activated carbon injection rate on mercury removal. All three variables were found to significantly impact the mercury removal efficiency in the pilot. The trends were clear: mercury removal rates increased with decreasing flue gas temperature and with increasing carbon injection rates. Mercury removal was much more efficient with reverse-gas and pulse-jet baghouse configurations than with an ESP as the particulate control device. The native fly ash of the host unit provided significant mercury removal capacity, so that the activated carbon sorbent served as an incremental mercury removal mechanism. Tests run to characterize the waste product, a combination of fly ash and activated carbon on which mercury was present, showed that mercury and other RCRA metals of interest were all below Toxic Characteristic Leaching Procedure (TCLP) regulatory limits in the leachate. The presence of activated carbon in the fly ash was shown to have an effect on the use of fly ash as an additive in the manufacture of concrete, which could limit the salability of fly ash from a plant where activated carbon was used for mercury control.

Jim Butz; Terry Hunt

2005-11-01T23:59:59.000Z

275

Cadmium, lead and mercury exposure in non smoking pregnant women  

SciTech Connect (OSTI)

Recent literature suggests that exposure to low concentrations of heavy metals may affect both maternal and child health. This study aimed to determine the biological heavy metals concentrations of pregnant women as well as environmental and dietary factors that may influence exposure concentrations. One hundred and seventy three pregnant women were recruited from Western Australia, each providing a sample of blood, first morning void urine, residential soil, dust and drinking water samples. Participants also completed a questionnaire which included a food frequency component. All biological and environmental samples were analysed for heavy metals using ICP-MS. Biological and environmental concentrations of lead and mercury were generally low (Median Pb Drinking Water (DW) 0.04 g/L; Pb soil <3.0 g/g; Pb dust 16.5 g/g; Pb blood 3.67 g/L; Pb urine 0.55; g/L Hg DW <0.03; Hg soil <1.0 g/g; Hg dust <1.0 g/g; Hg blood 0.46 g/L; Hg urine <0.40 g/L). Cadmium concentrations were low in environmental samples (Median CdDW 0.02 g/L; Cdsoil <0.30 ug/g; Cddust <0.30) but elevated in urine samples (Median 0.55 g/L, creatinine corrected 0.70 g/g (range <0.27.06 g/g creatinine) compared with other studies of pregnant women. Predictors of increased biological metals concentrations in regression models for blood cadmium were residing in the Great Southern region of Western Australia and not using iron/folic acid supplements and for urinary cadmium was having lower household annual income. However, these factors explained little of the variation in respective biological metals concentrations. The importance of establishing factors that influence low human exposure concentrations is becoming critical in efforts to reduce exposures and hence the potential for adverse health effects. -- Highlights: Biological heavy metals concentrations in women in their 3rd trimester of pregnancy. Exposure assessment including environmental, lifestyle and activity data. Urinary cadmium concentrations were elevated in this group of pregnant women. Blood lead and mercury concentrations were below recommended biological guideline values.

Hinwood, A.L., E-mail: a.hinwood@ecu.edu.au [Centre for Ecosystem Management, Edith Cowan University, 270 Joondalup Drive, Joondalup, WA 6027 (Australia); Callan, A.C.; Ramalingam, M.; Boyce, M. [Centre for Ecosystem Management, Edith Cowan University, 270 Joondalup Drive, Joondalup, WA 6027 (Australia)] [Centre for Ecosystem Management, Edith Cowan University, 270 Joondalup Drive, Joondalup, WA 6027 (Australia); Heyworth, J. [School Population Health, The University of Western Australia, 35 Stirling Highway Crawley, WA 6009 (Australia)] [School Population Health, The University of Western Australia, 35 Stirling Highway Crawley, WA 6009 (Australia); McCafferty, P. [ChemCentre, PO Box 1250, Bentley, WA 6983 (Australia)] [ChemCentre, PO Box 1250, Bentley, WA 6983 (Australia); Odland, J.. [Department of Community Medicine, University of Troms, N-9037 Troms (Norway)] [Department of Community Medicine, University of Troms, N-9037 Troms (Norway)

2013-10-15T23:59:59.000Z

276

In-situ subaqueous capping of mercury-contaminated sediments in a fresh-water aquatic system, Part II-evaluation of sorption materials  

SciTech Connect (OSTI)

The function and longevity of traditional, passive, isolation caps can be augmented through the use of more chemically active capping materials which have higher sorptive capacities, ideally rendering metals non-bioavailable. In the case of Hg, active caps also mitigate the rate and extent of methylation. This research examined low cost, readily available, capping materials for their ability to sequester Hg and MeHg. Furthermore, selected capping materials were evaluated to inhibit the methylation of Hg in an incubation study as well as the capacity of a selected capping material to inhibit translocation of Hg and MeHg with respect to ebullition-facilitated contaminant transport in a column study. Results indicated that bauxite had a better capacity for mercury sorption than the other test materials. However, bauxite as well as soil capping materials did not decrease methylation to a significant extent. Materials with larger surface areas, higher organic matter and acid volatile sulfide (AVS) content displayed a larger partitioning coefficient. In the incubation experiments, the presence of a carbon source (lactate), electron acceptor (sulfate) and the appropriate strains of SRB provided the necessary conditions for Hg methylation to occur. The column study showed effectiveness in sequestering Hg and MeHg and retarding transport to the overlying water column; however, disturbances to the soil capping material resulting from gas ebullition negated its effectiveness.

Randall, Paul M., E-mail: randall.paul@epa.gov [U.S. Environmental Protection Agency, Office of Research and Development, National Risk Management Research Laboratory, 26 W. Martin Luther King Drive, Cincinnati, OH 45268 (United States); Yates, Brian J.; Lal, Vivek; Darlington, Ramona [Battelle, 505 King Avenue, Columbus, OH 43201 (United States)] [Battelle, 505 King Avenue, Columbus, OH 43201 (United States); Fimmen, Ryan [Geosyntec Consultants, 150 E. Wilson Bridge Road, Suite 232, Worthington, OH 43085 (United States)] [Geosyntec Consultants, 150 E. Wilson Bridge Road, Suite 232, Worthington, OH 43085 (United States)

2013-08-15T23:59:59.000Z

277

RMP Mercury Strategy 06-03-09.doc Page 1 of 5 RMP MERCURY STRATEGY  

E-Print Network [OSTI]

RMP Mercury Strategy 06-03-09.doc Page 1 of 5 RMP MERCURY STRATEGY Mercury is a pollutant of high the information most urgently needed by managers to find remedies to the Bay's mercury problem. The focus of total mercury in the Bay are expected to slowly decline over coming decades. The premise

278

MERCURY EMISSIONS FROM COAL FIRED POWER PLANTS LOCAL IMPACTS ON HUMAN HEALTH RISK.  

SciTech Connect (OSTI)

A thorough quantitative understanding of the processes of mercury emissions, deposition, and translocation through the food chain is currently not available. Complex atmospheric chemistry and dispersion models are required to predict concentration and deposition contributions, and aquatic process models are required to predict effects on fish. However, there are uncertainties in all of these predictions. Therefore, the most reliable method of understanding impacts of coal-fired power plants on Hg deposition is from empirical data. A review of the literature on mercury deposition around sources including coal-fired power plants found studies covering local mercury concentrations in soil, vegetation, and animals (fish and cows). There is strong evidence of enhanced local deposition within 3 km of the chlor-alkali plants, with elevated soil concentrations and estimated deposition rates of 10 times background. For coal-fired power plants, the data show that atmospheric deposition of Hg may be slightly enhanced. On the scale of a few km, modeling suggests that wet deposition may be increased by a factor of two or three over background. The measured data suggest lower increases of 15% or less. The effects of coal-fired plants seem to be less than 10% of total deposition on a national scale, based on emissions and global modeling. The following summarizes our findings from published reports on the impacts of local deposition. In terms of excesses over background the following increments have been observed within a few km of the plant: (1) local soil concentration Hg increments of 30%-60%, (2) sediment increments of 18-30%, (3) wet deposition increments of 11-12%, and (4) fish Hg increments of about 5-6%, based on an empirical finding that fish concentrations are proportional to the square root of deposition. Important uncertainties include possible reductions of RGM to Hg{sub 0} in power plant plumes and the role of water chemistry in the relationship between Hg deposition and fish content. Soil and vegetation sampling programs were performed around two mid-size coal fired power plants. The objectives were to determine if local mercury hot-spots exist, to determine if they could be attributed to deposition of coal-fired power plant emissions, and to determine if they correlated with model predictions. These programs found the following: (1) At both sites, there was no correlation between modeled mercury deposition and either soil concentrations or vegetation concentrations. At the Kincaid plant, there was excess soil Hg along heavily traveled roads. The spatial pattern of soil mercury concentrations did not match the pattern of vegetation Hg concentrations at either plant. (2) At both sites, the subsurface (5-10 cm) samples the Hg concentration correlated strongly with the surface samples (0-5 cm). Average subsurface sample concentrations were slightly less than the surface samples; however, the difference was not statistically significant. (3) An unequivocal definition of background Hg was not possible at either site. Using various assumed background soil mercury concentrations, the percentage of mercury deposited within 10 km of the plant ranged between 1.4 and 8.5% of the RGM emissions. Based on computer modeling, Hg deposition was primarily RGM with much lower deposition from elemental mercury. Estimates of the percentage of total Hg deposition ranged between 0.3 and 1.7%. These small percentages of deposition are consistent with the empirical findings of only minor perturbations in environmental levels, as opposed to ''hot spots'', near the plants. The major objective of this study was to determine if there was evidence for ''hot-spots'' of mercury deposition around coal-fired power plants. Although the term has been used extensively, it has never been defined. From a public health perspective, such a ''hot spot'' must be large enough to insure that it did not occur by chance, and it must affect water bodies large enough to support a population of subsistence fishers. The results of this study support the hypothesis that n

SULLIVAN, T.M.; BOWERMAN, B.; ADAMS, J.; LIPFERT, F.; MORRIS, S.M.; BANDO, A.; PENA, R.; BLAKE, R.

2005-12-01T23:59:59.000Z

279

Summary - Mitigation and Remediation of Mercury Contamination...  

Office of Environmental Management (EM)

and surface water Hg remediation strategy for adequacy in reducing Hg levels in the fish and to indentify opportunities to achieve cost and technical improvements andor to...

280

Stanford University Mercury Thermometer Replacement  

E-Print Network [OSTI]

Stanford University Mercury Thermometer Replacement Program Instructions for Reuniting Separated Fluid Column of Non-Mercury Thermometer Heating Method Heat the thermometers bulb in an upright position of the thermometer. Note that over filling the expansion chamber will break the thermometer. Tap the thermometer

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


281

Sulfur Polymer Stabilization/Solidification Treatability Study of Mercury Contaminated Soil from the Y-12 Site  

SciTech Connect (OSTI)

As a result of past operations, the Department of Energys (DOE) Oak Ridge Y-12 National Security Complex (Y-12 Plant) has extensive mercury-contamination in building structures, soils, storm sewer sediments, and stream sediments, which are a source of pollution to the local ecosystem. Because of mercurys toxicity and potential impacts on human health and the environment, DOE continues to investigate and implement projects to support the remediation of the Y-12 site.URS and #9122;CH2M Oak Ridge LLC (UCOR) under its prime contract with DOE has cleanup responsibilities on the DOE Oak Ridge Reservation and is investigating potential mercury-contaminated soil treatment technologies through an agreement with Babcock and Wilcox (B and W) Y-12, the Y-12 operating contractor to DOE. As part of its investigations, UCOR has subcontracted with Brookhaven National Laboratory (BNL) to conduct laboratory-scale studies evaluating the applicability of the Sulfur Polymer Stabilization/Solidification (SPSS) process using surrogate and actual mixed waste Y-12 soils containing mercury (Hg) at 135, 2,000, and 10,000 ppm.SPSS uses a thermoplastic sulfur binder to convert Hg to stable mercury sulfide (HgS) and solidifies the chemically stable product in a monolithic solid final waste form to reduce dispersion and permeability. Formulations containing 40 60 dry wt% Y-12 soil were fabricated and samples were prepared in triplicate for Environmental Protection Agency Toxicity Characteristic Leaching Procedure (TCLP) testing by an independent laboratory. Those containing 50 and 60 wt% soil easily met the study criteria for maximum allowable Hg concentrations (47 and 1 ppb, respectively compared with the TCLP limit of 200 ppb Hg). The lowest waste loading of 40 wt% yielded TCLP Hg concentrations slightly higher (240 ppb) than the allowable limit. Since the Y-12 soil tended to form clumps, the improved leaching at higher waste loadings was probably due to reduction in particle size from friction of the soil mixing, which creates more surface area for chemical conversion. This was corroborated by the fact that the same waste loading pre-treated by ball milling to reduce particle size prior to SPSS processing yielded TCLP concentrations almost 30 times lower, and at 8.5 ppb Hg was well below EPA limits. Pre-treatment by ball milling also allowed a reduction in the time required for stabilization, thus potentially reducing total process times by 30%.Additional performance testing was conducted including measurement of compressive strength to confirm mechanical integrity and immersion testing to determine the potential impacts of storage or disposal under saturated conditions. For both surrogate and actual Y-12 treated soils, waste form compressive strengths ranged between 2,300 and 6,500 psi, indicating very strong mechanical integrity (a minimum of greater than 40 times greater than the NRC guidance for low-level radioactive waste). In general, compressive strength increases with waste loading as the soil acts as an aggregate in the sulfur concrete waste forms. No statistically significant loss in strength was recorded for the 30 and 40 wt% surrogate waste samples and only a minor reduction in strength was measured for the 43 wt% waste forms. The 30 wt% Y-12 soil did not show a significant loss in strength but the 50 wt% samples were severely degraded in immersion due to swelling of the clay soil. The impact on Hg leaching, if any, was not determined.

Kalb P.; Milian, L.; Yim, S. P.

2012-11-30T23:59:59.000Z

282

Atmospheric Mercury: Emissions, Transport/Fate,  

E-Print Network [OSTI]

, global...) Is "emissions trading" workable and ethical? Is the recently promulgated Clean Air Mercury

283

Mercury Speciation in the Presence of Polysulfides  

E-Print Network [OSTI]

Mercury Speciation in the Presence of Polysulfides J E N N Y A Y L A J A Y , * , F R A N C¸ O I Environmental mercury methylation appears modulated by sulfide concentrations, possibly via changes in mercury, there has been much recent interest in quantifying the chemical speciation and lipid solubility of mercury

Morel, François M. M.

284

Mercury and the Gold Country Angler Survey  

E-Print Network [OSTI]

#12;#12;Mercury and the Gold Rush #12;#12;#12;#12;#12;#12;#12;#12;#12;Gold Country Angler Survey A Pilot Study to Assess Mercury Exposure from Sport Fish Consumption in the Sierra Nevada Carrie Monohan, Ph.D. #12;Mercury and the Gold Rush Deer Creek 1908 Greenhorn Creek 2011 Mercury was used during

285

Mercury Pollution in the Marine Environment  

E-Print Network [OSTI]

Mercury Pollution in the Marine Environment The Coastal and Marine Mercury Ecosystem Research stakeholders to form C-MERC, the Coastal and Marine Mercury Ecosystem Research Collaborative. The goal was to review current knowledge--and knowledge gaps--relating to a global environmental health problem, mercury

Shepherd, Simon

286

Mercury Isotope Fractionation by Environmental Transport and Transformation Processes  

E-Print Network [OSTI]

measurements of atomic mercury. Applied Physics B, 87(2),M. & Covelli, S. , 2000. Mercury speciation in sedimentsarea of the Idrija mercury mine, Slovenia. Environmental

Koster van Groos, Paul Gijsbert

2011-01-01T23:59:59.000Z

287

Waste Coal Fines Reburn for NOx and Mercury Emission Reduction  

SciTech Connect (OSTI)

Injection of coal-water slurries (CWS) made with both waste coal and bituminous coal was tested for enhanced reduction of NO{sub x} and Hg emissions at the AES Beaver Valley plant near Monaca, PA. Under this project, Breen Energy Solutions (BES) conducted field experiments on the these emission reduction technologies by mixing coal fines and/or pulverized coal, urea and water to form slurry, then injecting the slurry in the upper furnace region of a coal-fired boiler. The main focus of this project was use of waste coal fines as the carbon source; however, testing was also conducted using pulverized coal in conjunction with or instead of waste coal fines for conversion efficiency and economic comparisons. The host site for this research and development project was Unit No.2 at AES Beaver Valley cogeneration station. Unit No.2 is a 35 MW Babcock & Wilcox (B&W) front-wall fired boiler that burns eastern bituminous coal. It has low NO{sub x} burners, overfire air ports and a urea-based selective non-catalytic reduction (SNCR) system for NO{sub x} control. The back-end clean-up system includes a rotating mechanical ash particulate removal and electrostatic precipitator (ESP) and wet flue gas desulfurization (FGD) scrubber. Coal slurry injection was expected to help reduce NOx emissions in two ways: (1) Via fuel-lean reburning when the slurry is injected above the combustion zone. (2) Via enhanced SNCR reduction when urea is incorporated into the slurry. The mercury control process under research uses carbon/water slurry injection to produce reactive carbon in-situ in the upper furnace, promoting the oxidation of elemental mercury in flue gas from coal-fired power boilers. By controlling the water content of the slurry below the stoichiometric requirement for complete gasification, water activated carbon (WAC) can be generated in-situ in the upper furnace. As little as 1-2% coal/water slurry (heat input basis) can be injected and generate sufficient WAC for mercury capture. During July, August, and September 2007, BES designed, procured, installed, and tested the slurry injection system at Beaver Valley. Slurry production was performed by Penn State University using equipment that was moved from campus to the Beaver Valley site. Waste coal fines were procured from Headwaters Inc. and transported to the site in Super Sacks. In addition, bituminous coal was pulverized at Penn State and trucked to the site in 55-gallon drums. This system was operated for three weeks during August and September 2007. NO{sub x} emission data were obtained using the plant CEM system. Hg measurements were taken using EPA Method 30B (Sorbent Trap method) both downstream of the electrostatic precipitator and in the stack. Ohio Lumex Company was on site to provide rapid Hg analysis on the sorbent traps during the tests. Key results from these tests are: (1) Coal Fines reburn alone reduced NO{sub x} emissions by 0-10% with up to 4% heat input from the CWS. However, the NO{sub x} reduction was accompanied by higher CO emissions. The higher CO limited our ability to try higher reburn rates for further NO{sub x} reduction. (2) Coal Fines reburn with Urea (Carbon enhanced SNCR) decreased NO{sub x} emissions by an additional 30% compared to Urea injection only. (3) Coal slurry injection did not change Hg capture across the ESP at full load with an inlet temperature of 400-430 F. The Hg capture in the ESP averaged 40%, with or without slurry injection; low mercury particulate capture is normally expected across a higher temperature ESP because any oxidized mercury is thought to desorb from the particulate at ESP temperatures above 250 F. (4) Coal slurry injection with halogen salts added to the mixing tank increased the Hg capture in the ESP to 60%. This significant incremental mercury reduction is important to improved mercury capture with hot-side ESP operation and wherever hindrance from sulfur oxides limit mercury reduction, because the higher temperature is above sulfur oxide dew point interference.

Stephen Johnson; Chetan Chothani; Bernard Breen

2008-04-30T23:59:59.000Z

288

EVALUATION OF MERCURY EMISSIONS FROM COAL-FIRED FACILITIES WITH SCR AND FGD SYSTEMS  

SciTech Connect (OSTI)

CONSOL Energy Inc., Research & Development (CONSOL), with support from the U.S. Department of Energy, National Energy Technology Laboratory (DOE) and the Electric Power Research Institute (EPRI), evaluated the effects of selective catalytic reduction (SCR) on mercury (Hg) capture in coal-fired plants equipped with an electrostatic precipitator (ESP)-wet flue gas desulfurization (FGD) combination or a spray dyer absorber-fabric filter (SDA-FF) combination. In this program CONSOL determined mercury speciation and removal at 10 bituminous coal-fired facilities; at four of these facilities, additional tests were performed on units without SCR, or with the existing SCR bypassed. This project final report summarizes the results and discusses the findings of the body of work as a whole. Eleven Topical Reports were issued (prior to this report) that describe in great detail the sampling results at each of the ten power plants individually. The results showed that the SCR-FGD combination removed a substantial fraction of mercury from flue gas. The coal-to-stack mercury removals ranged from 65% to 97% for the units with SCR and from 53% to 87% for the units without SCR. There was no indication that any type of FGD system was more effective at mercury removal than others. The coal-to-stack mercury removal and the removal in the wet scrubber were both negatively correlated with the elemental mercury content of the flue gas and positively correlated with the scrubber liquid chloride concentration. The coal chlorine content was not a statistically significant factor in either case. Mercury removal in the ESP was positively correlated with the fly ash carbon content and negatively correlated with the flue gas temperature. At most of the units, a substantial fraction (>35%) of the flue gas mercury was in the elemental form at the boiler economizer outlet. After passing through the SCR-air heater combination very little of the total mercury (<10%) remained in the elemental form in the flue gas; this was true for all SCR catalyst types and sources. Although chlorine has been suggested as a factor affecting the mercury speciation in flue gas, coal chlorine was not a statistically significant factor affecting mercury speciation at the economizer exit or at the air heater exit. The only statistically significant factors were the coal ash CaO content and the fly ash carbon content; the fraction of mercury in the elemental form at the economizer exit was positively correlated with both factors. In a direct comparison at four SCR-equipped units vs. similar units at the same sites without SCR (or with the SCR bypassed), the elemental mercury fractions (measured at the ESP outlet) were lower, and the coal-to-stack mercury removals were higher, when the SCR was present and operating. The average coal-to-stack mercury removal at the four units without an operating SCR was 72%, whereas the average removal at the same sites with operating SCRs was 88%. The unit mercury mass balance (a gauge of the overall quality of the tests) at all of the units ranged from 81% to 113%, which were within our QA/QC criterion of 80-120%.

J.A. Withum

2006-03-07T23:59:59.000Z

289

Multi-Pollutant Emissions Control: Pilot Plant Study of Technologies for Reducing Hg, SO3, NOx and CO2 Emissions  

SciTech Connect (OSTI)

A slipstream pilot plant was built and operated to investigate technology to adsorb mercury (Hg) onto the existing particulate (i.e., fly ash) by cooling flue gas to 200-240 F with a Ljungstrom-type air heater or with water spray. The mercury on the fly ash was then captured in an electrostatic precipitator (ESP). An alkaline material, magnesium hydroxide (Mg(OH){sub 2}), is injected into flue gas upstream of the air heater to control sulfur trioxide (SO{sub 3}), which prevents acid condensation and corrosion of the air heater and ductwork. The slipstream was taken from a bituminous coal-fired power plant. During this contract, Plant Design and Construction (Task 1), Start Up and Maintenance (Task 2), Baseline Testing (Task 3), Sorbent Testing (Task 4), Parametric Testing (Task 5), Humidification Tests (Task 6), Long-Term Testing (Task 7), and a Corrosion Study (Task 8) were completed. The Mercury Stability Study (Task 9), ESP Report (Task 11), Air Heater Report (Task 12) and Final Report (Task 14) were completed. These aspects of the project, as well as progress on Public Outreach (Task 15), are discussed in detail in this final report. Over 90% mercury removal was demonstrated by cooling the flue gas to 200-210 F at the ESP inlet; baseline conditions with 290 F flue gas gave about 26% removal. Mercury removal is sensitive to flue gas temperature and carbon content of fly ash. At 200-210 F, both elemental and oxidized mercury were effectively captured at the ESP. Mg(OH){sub 2} injection proved effective for removal of SO{sub 3} and eliminated rapid fouling of the air heater. The pilot ESP performed satisfactorily at low temperature conditions. Mercury volatility and leaching tests did not show any stability problems. No significant corrosion was detected at the air heater or on corrosion coupons at the ESP. The results justify larger-scale testing/demonstration of the technology. These conclusions are presented and discussed in two presentations given in July and September of 2005 and are included in Appendices E and F.

Michael L. Fenger; Richard A. Winschel

2005-08-31T23:59:59.000Z

290

EFFECTS OF FLY ASH ON MERCURY OXIDATION DURING POST COMBUSTION CONDITIONS  

SciTech Connect (OSTI)

Tests were performed in simulated flue gas streams using two fly ash samples from the electrostatic precipitators of two full-scale utility boilers. One fly ash was derived from a Powder River Basin (PRB) coal, while the other was derived from Blacksville coal (Pittsburgh No. 8 seam). The tests were performed at temperatures of 120 and 180 C under different gas compositions. Elemental mercury (Hg) streams were injected into the simulated flue gas and passed over filters (housed in a convection oven) loaded with fly ash. The Ontario Hydro method was used to determine the total amount of Hg passing through the filter as well as the percentages of elemental and oxidized Hg collected. Results indicated that substantial amounts of Hg oxidation did not occur with either fly ash, regardless of the temperature used for testing. When oxidation was observed, the magnitude of the oxidation was comparable between the two fly ashes. These results suggest that the gas matrix may be more important than the ash components with respect to the distribution of Hg species observed in gaseous effluents at coal-fired power plants.

Glenn A. Norton

1999-10-01T23:59:59.000Z

291

U01HG004279 (D.M.M.), U01HG004261 (E.L.), U01HG004274 (S.H.), and U41HG004269 (L.S.). Awards  

E-Print Network [OSTI]

.T.N.), the Indiana Genomics Initiative (T.C.K.), H. Smith and the NIDDK genomics core laboratory (B.O.), NIH R01HG

292

Mercury's moment of inertia from spin and gravity data  

E-Print Network [OSTI]

2006), Evolution of Mercurys obliquity, Icarus, 181, 327longitude librations of Mercury, Icarus, 207, 11 of 11The free librations of Mercury and the size of its inner

2012-01-01T23:59:59.000Z

293

Gasoline vapor recovery  

SciTech Connect (OSTI)

In a gasoline distribution network wherein gasoline is drawn from a gasoline storage tank and pumped into individual vehicles and wherein the gasoline storage tank is refilled periodically from a gasoline tanker truck, a method of recovering liquid gasoline from gasoline vapor that collects in the headspace of the gasoline storage tank as the liquid gasoline is drawn therefrom, said method comprising the steps of: (a) providing a source of inert gas; (b) introducing inert gas into the gasoline storage tank as liquid gasoline is drawn therefrom so that liquid gasoline drawn from the tank is displaced by inert gas and gasoline vapor mixes with the inert gas in the headspace of the tank; (c) collecting the inert gas/gasoline vapor mixture from the headspace of the gasoline storage tank as the tank is refilled from a gasoline tanker truck; (d) cooling the inert gas/gasoline vapor mixture to a temperature sufficient to condense the gasoline vapor in the mixture to liquid gasoline but not sufficient to liquify the inert gas in the mixture; (e) separating the condensed liquid gasoline from the inert gas; and delivering the condensed liquid gasoline to a remote location for subsequent use.

Lievens, G.; Tiberi, T.P.

1993-06-22T23:59:59.000Z

294

Fate of Mercury in Synthetic Gypsum Used for Wallboard Production  

SciTech Connect (OSTI)

This report presents and discusses results from the project 'Fate of Mercury in Synthetic Gypsum Used for Wallboard Production', performed at five different full-scale commercial wallboard plants. Synthetic gypsum produced by wet flue gas desulfurization (FGD) systems on coal-fired power plants is commonly used in the manufacture of wallboard. This practice has long benefited the environment by recycling the FGD gypsum byproduct, which is becoming available in increasing quantities, decreasing the need to landfill this material, and increasing the sustainable design of the wallboard product. However, new concerns have arisen as recent mercury control strategies involve the capture of mercury in FGD systems. The objective of this study has been to determine whether any mercury is released into the atmosphere at wallboard manufacturing plants when the synthetic gypsum material is used as a feedstock for wallboard production. The project has been co-funded by the U.S. DOE National Energy Technology Laboratory (Cooperative Agreement DE-FC26-04NT42080), USG Corporation, and EPRI. USG Corporation is the prime contractor, and URS Group is a subcontractor. The project scope included seven discrete tasks, each including a test conducted at various USG wallboard plants using synthetic gypsum from different wet FGD systems. The project was originally composed of five tasks, which were to include (1) a base-case test, then variations representing differing power plant: (2) emissions control configurations, (3) treatment of fine gypsum particles, (4) coal types, and (5) FGD reagent types. However, Task 5,could not be conducted as planned and instead was conducted at conditions similar to Task 3. Subsequently an opportunity arose to test gypsum produced from the Task 5 FGD system, but with an additive expected to impact the stability of mercury, so Task 6 was added to the project. Finally, Task 7 was added to evaluate synthetic gypsum produced at a power plant from an additional coal type. In the project, process stacks in the wallboard plant were sampled using the Ontario Hydro method. In every task, the stack locations sampled included a gypsum dryer and a gypsum calciner. In Tasks 1 and 4 through 7, the stack of the dryer for the wet wallboard product was also tested. Also at each site, in-stream process samples were collected and analyzed for mercury concentration before and after each significant step in wallboard production. These results and process data were used to construct mercury mass balances across the wallboard plants. The results from the project showed a wide range of percentage mercury losses from the synthetic gypsum feedstocks as measured by the Ontario Hydro method at the process stacks, ranging from 2% to 55% of the mercury in the gypsum feedstock. For the tasks exceeding 10% mercury loss across the wallboard plant, most of the loss occurred across the gypsum calciner. When total wallboard emissions remained below 10%, the primary emission location varied with a much less pronounced difference in emission between the gypsum dryer, calciner and board dryer. For all seven tasks, the majority of the mercury emissions were measured to be in the elemental form (Hg{sup 0}). Overall, the measured mercury loss mass rates ranged from 0.01 to 0.17 grams of mercury per dry ton of synthetic gypsum processed, or 0.01 to 0.4 pounds of mercury released per million square feet of wallboard produced from synthetic gypsum. The Coal Combustion Product Production and Use Survey from the American Coal Ash Association (ACAA) indicate that 7,579,187 short tons of synthetic gypsum were used for wallboard production in 2006. Extrapolating the results of this study to the ACAA industry usage rate, we estimate that mercury releases from wallboard production plants in 2006 ranged between 150 to 3000 pounds for the entire U.S. wallboard industry. With only seven sets of wallboard plant measurements, it is difficult to draw firm conclusions about what variables impact the mercury loss percentages across the wallboard plants. One significant o

Jessica Sanderson

2007-12-31T23:59:59.000Z

295

Mercury in the Anthropocene Ocean  

E-Print Network [OSTI]

The toxic metal mercury is present only at trace levels in the ocean, but it accumulates in fish at concentrations high enough to pose a threat to human and environmental health. Human activity has dramatically altered the ...

Lamborg, Carl

296

Study of mercury oxidation by a selective catalytic reduction catalyst in a pilot-scale slipstream reactor at a utility boiler burning bituminous coal  

SciTech Connect (OSTI)

One of the cost-effective mercury control technologies in coal-fired power plants is the enhanced oxidation of elemental mercury in selective catalytic reduction (SCR) followed by the capture of the oxidized mercury in the wet scrubber. This paper is the first in a series of two in which the validation of the SCR slipstream test and Hg speciation variation in runs with or without SCR catalysts inside the SCR slipstream reactor under special gas additions (HCl, Cl{sub 2}, SO{sub 2}, and SO{sub 3}) are presented. Tests indicate that the use of a catalyst in a SCR slipstream reactor can achieve greater than 90% NO reduction efficiency with a NH{sub 3}/NO ratio of about 1. There is no evidence to show that the reactor material affects mercury speciation. Both SCR catalysts used in this study exhibited a catalytic effect on the elemental mercury oxidation but had no apparent adsorption effect. SCR catalyst 2 seemed more sensitive to the operational temperature. The spike gas tests indicated that HCl can promote Hg{sup 0} oxidation but not Cl{sub 2}. The effect of Cl{sub 2} on mercury oxidation may be inhibited by higher concentrations of SO{sub 2}, NO, or H{sub 2}O in real flue-gas atmospheres within the typical SCR temperature range (300-350{sup o}C). SO{sub 2} seemed to inhibit mercury oxidation; however, SO{sub 3} may have some effect on the promotion of mercury oxidation in runs with or without SCR catalysts. 25 refs., 9 figs., 2 tabs.

Yan Cao; Bobby Chen; Jiang Wu; Hong Cui; John Smith; Chi-Kuan Chen; Paul Chu; Wei-Ping Pan [Western Kentucky University, Bowling Green, KY (United States). Institute for Combustion Science and Environmental Technology (ICSET)

2007-01-15T23:59:59.000Z

297

Electrolyte vapor condenser  

DOE Patents [OSTI]

A system is disclosed for removing electrolyte from a fuel cell gas stream. The gas stream containing electrolyte vapor is supercooled utilizing conventional heat exchangers and the thus supercooled gas stream is passed over high surface area passive condensers. The condensed electrolyte is then drained from the condenser and the remainder of the gas stream passed on. The system is particularly useful for electrolytes such as phosphoric acid and molten carbonate, but can be used for other electrolyte cells and simple vapor separation as well. 3 figs.

Sederquist, R.A.; Szydlowski, D.F.; Sawyer, R.D.

1983-02-08T23:59:59.000Z

298

Electrolyte vapor condenser  

DOE Patents [OSTI]

A system is disclosed for removing electrolyte from a fuel cell gas stream. The gas stream containing electrolyte vapor is supercooled utilizing conventional heat exchangers and the thus supercooled gas stream is passed over high surface area passive condensers. The condensed electrolyte is then drained from the condenser and the remainder of the gas stream passed on. The system is particularly useful for electrolytes such as phosphoric acid and molten carbonate, but can be used for other electrolyte cells and simple vapor separation as well.

Sederquist, Richard A. (Newington, CT); Szydlowski, Donald F. (East Hartford, CT); Sawyer, Richard D. (Canton, CT)

1983-01-01T23:59:59.000Z

299

Growth of superconducting Hg-1212 very-thin films  

E-Print Network [OSTI]

High quality epitaxial HgBa2CaCu2O6+delta (Hg- High 1212) films with thickness less than 100 nm have been successfully synthesized using cation-exchange process. The films show the superconducting transition up to similar to 118 K which is close...

Wu, Judy; Xie, Y. Y.; Kang, B. W.; Gapud, A. A.; Aytug, T.; Fang, L.

1999-06-01T23:59:59.000Z

300

The helium abundances in HgMn and normal stars  

E-Print Network [OSTI]

The parameter-free model of diffusion in the atmospheres of HgMn stars (Michaud 1986; Michaud et al 1979) predicts that helium should sink below the He II ionization zone in order that diffusion of other elements may take place, and that all HgMn stars should have deficits of helium in their photospheres, with a minimum deficit of 0.3 dex. In this study, the Smith & Dworetsky (1993) sample of HgMn stars and normal comparison stars is examined, and the helium abundances determined by spectrum synthesis using echelle spectra taken at Lick Observatory and the AAT. The prediction is confirmed; all HgMn stars are deficient in He by as much as 1.5 dex. Also, two HgMn stars, HR7361 and HR7664, show clear evidence of helium stratification.

M. M. Dworetsky

2004-07-26T23:59:59.000Z

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


301

IntroductionIntroduction Mercury: Monitoring Patients with ParkinsonMercury: Monitoring Patients with Parkinson''s Diseases Disease  

E-Print Network [OSTI]

IntroductionIntroduction Mercury: Monitoring Patients with ParkinsonMercury: Monitoring Patients's Disease EvaluationEvaluation Mercury ArchitectureMercury Architecture Mercury is a wireless sensor network and disconnections Node Behavior Hardware PlatformHardware Platform Usage Scenario InternetInternet http://fiji.eecs.harvard.edu/Mercury

Chen, Yiling

302

Mercury in Fish Collected Upstream and Downstream of Los Alamos National Laboratory, New Mexico: 1991--2004.  

SciTech Connect (OSTI)

Small amounts of mercury (Hg) may exist in some canyon drainage systems within Los Alamos National Laboratory lands as a result of past discharges of untreated effluents. This paper reports on the concentrations of Hg in muscle (fillets) of various types of fish species collected downstream of LANL's influence from 1991 through 2004. The mean Hg concentration in fish from Cochiti reservoir (0.22 {micro}g/g wet weight), which is located downstream of LANL, was similar to fish collected from a reservoir upstream of LANL (Abiquiu) (0.26 {micro}g/g wet weight). Mercury concentrations in fish collected from both reservoirs exhibited significantly (Abiquiu = p < 0.05 and Cochiti = p < 0.10) decreasing trends over time. Predator fish like the northern pike (Esox lucius) contained significantly higher concentrations of Hg (0.39 {micro}g/g wet weight) than bottom-feeding fish like the white sucker (Catostomus commersoni) (0.10 {micro}g/g wet weight).

P.R. Fresquez

2004-10-15T23:59:59.000Z

303

Modeling CO{sub 2}-Brine-Rock Interaction Including Mercury and H{sub 2}S Impurities in the Context of CO{sub 2} Geologic Storage  

SciTech Connect (OSTI)

This study uses modeling and simulation approaches to investigate the impacts on injectivity of trace amounts of mercury (Hg) in a carbon dioxide (CO{sub 2}) stream injected for geologic carbon sequestration in a sandstone reservoir at ~2.5 km depth. At the range of Hg concentrations expected (7-190 ppbV, or ~ 0.06-1.6 mg/std.m{sup 3}CO{sub 2}), the total volumetric plugging that could occur due to complete condensation of Hg, or due to complete precipitation of Hg as cinnabar, results in a very small porosity change. In addition, Hg concentration much higher than the concentrations considered here would be required for Hg condensation to even occur. Concentration of aqueous Hg by water evaporation into CO{sub 2} is also unlikely because the higher volatility of Hg relative to H{sub 2}O at reservoir conditions prevents the Hg concentration from increasing in groundwater as dry CO{sub 2} sweeps through, volatilizing both H{sub 2}O and Hg. Using a model-derived aqueous solution to represent the formation water, batch reactive geochemical modeling show that the reaction of the formation water with the CO{sub 2}-Hg mixture causes the pH to drop to about 4.7 and then become buffered near 5.2 upon reaction with the sediments, with a negligible net volume change from mineral dissolution and precipitation. Cinnabar (HgS(s)) is found to be thermodynamically stable as soon as the Hg-bearing CO{sub 2} reacts with the formation water which contains small amounts of dissolved sulfide. Liquid mercury (Hg(l)) is not found to be thermodynamically stable at any point during the simulation. Two-dimensional radial reactive transport simulations of CO{sub 2} injection at a rate of 14.8 kg/s into a 400 m-thick formation at isothermal conditions of 106C and average pressure near 215 bar, with varying amounts of Hg and H{sub 2}S trace gases, show generally that porosity changes only by about 0.05% (absolute, i.e., new porosity = initial porosity 0.0005) with Hg predicted to readily precipitate from the CO{sub 2} as cinnabar in a zone mostly matching the single-phase CO{sub 2} plume. The precipitation of minerals other than cinnabar, however, dominates the evolution of porosity. Main reactions include the replacement of primarily Fe-chlorite by siderite, of calcite by dolomite, and of K-feldspar by muscovite. Chalcedony is also predicted to precipitate from the dissolution of feldspars and quartz. Although the range of predicted porosity change is quite small, the amount of dissolution and precipitation predicted for these individual minerals is not negligible. These reactive transport simulations assume that Hg gas behaves ideally. To examine effects of non-ideality on these simulations, approximate calculations of the fugacity coefficient of Hg in CO{sub 2} were made. Results suggest that Hg condensation could be significantly overestimated when assuming ideal gas behavior, making our simulation results conservative with respect to impacts on injectivity. The effect of pressure on Henrys constant for Hg is estimated to yield Hg solubilities about 10% lower than when this effect is not considered, a change that is considered too small to affect the conclusions of this report. Although all results in this study are based on relatively mature data and modeling approaches, in the absence of experimental data and more detailed site-specific information, it is not possible to fully validate the results and conclusions.

Spycher, N.; Oldenburg, C.M.

2014-01-01T23:59:59.000Z

304

JV Task 124 - Understanding Multi-Interactions of SO3, Mercury, Selenium, and Arsenic in Illinois Coal Flue Gas  

SciTech Connect (OSTI)

This project consisted of pilot-scale combustion testing with a representative Illinois basin coal to explore the multi-interactions of SO{sub 3}, mercury, selenium and arsenic. The parameters investigated for SO{sub 3} and mercury interactions included different flue gas conditions, i.e., temperature, moisture content, and particulate alkali content, both with and without activated carbon injection for mercury control. Measurements were also made to track the transformation of selenium and arsenic partitioning as a function of flue gas temperature through the system. The results from the mercury-SO{sub 3} testing support the concept that SO{sub 3} vapor is the predominant factor that impedes efficient mercury removal with activated carbon in an Illinois coal flue gas, while H{sub 2}SO{sub 4} aerosol has less impact on activated carbon injection performance. Injection of a suitably mobile and reactive additives such as sodium- or calcium-based sorbents was the most effective strategy tested to mitigate the effect of SO{sub 3}. Transformation measurements indicate a significant fraction of selenium was associated with the vapor phase at the electrostatic precipitator inlet temperature. Arsenic was primarily particulate-bound and should be captured effectively with existing particulate control technology.

Ye Zhuang; Christopher Martin; John Pavlish

2009-03-31T23:59:59.000Z

305

EFFECTS OF FLY ASH ON MERCURY OXIDATION DURING POST COMBUSTION CONDITIONS  

SciTech Connect (OSTI)

Tests were performed in simulated flue gas streams using fly ash from the electrostatic precipitators of two full-scale utility boilers. One fly ash was from a Powder River Basin (PRB) coal, while the other was from Blacksville coal. Elemental Hg was injected upstream from samples of fly ash loaded onto filters housed in an oven at 120 or 180 C. Concentrations of oxidized and elemental Hg downstream from the filters were determined using the Ontario Hydro method. The gas stream composition and whether or not ash was present in the gas stream were the two most important variables affecting Hg oxidation. The presence of HCl, NO, NO{sub 2}, and SO{sub 2} were all important with respect to Hg oxidation, with NO{sub 2} and HCl being the most important. The presence of NO suppressed Hg oxidation in these tests. Although the two fly ashes were chemically and mineralogically diverse, there were generally no large differences in catalytic potential (for oxidizing Hg) between them. Similarly, no ash fraction appeared to be highly catalytic relative to other ash fractions. This includes fractions enriched in unburned carbon and fractions enriched in iron oxides. Although some differences of lesser magnitude were observed in the amount of oxidized Hg formed, levels of oxidized Hg generally tracked well with the surface areas of the different ashes and ash fractions. Therefore, although the Blacksville fly ash tended to show slightly more catalytic activity than the PRB fly ash, this could be due to the relatively high surface area of that ash. Similarly, for Blacksville fly ash, using nonmagnetic ash resulted in more Hg oxidation than using magnetic ash, but this again tracked well with the relative surface areas of the two ash fractions. Test results suggest that the gas matrix may be more important in Hg oxidation chemistry than the fly ash composition. Combustion tests were performed in which Blacksville and PRB fly ashes were injected into filtered (via a baghouse with Teflon bags) flue gas obtained while firing PRB coal in a 35 kW combustor. The Ontario Hydro method was used to determine the Hg speciation after fly ash injection. Wall effects in the combustor complicated interpretation of testing data, although a number of observations could still be made. The amount of Hg collected in the Ontario Hydro impingers was lower than anticipated, and is probably due to sorption of Hg by the fly ash. While firing PRB coal without any ash injection, the percent oxidized Hg in the gas stream was fairly high (average of 63%). The high levels of vapor phase oxidized Hg in these base line tests may be due to catalytic effects from the refractory materials in the combustor. When PRB fly ash was injected into a filtered PRB flue gas stream, the percentage of oxidized Hg in the gas stream decreased dramatically. Decreases in the percentage of oxidized Hg were also observed while injecting Blacksville fly ash, but to a lesser extent. Injecting whole Blacksville fly ash into the filtered PRB flue gas appeared to result in greater concentrations of oxidized Hg relative to the tests where whole PRB fly ash was injected. However, because the Blacksville fly ash has a relatively high surface area, this may be only a surface area effect.

Glenn A. Norton; Hongqun Yang; Robert C. Brown; Dennis L. Laudal; Grant E. Dunham; John Erjavec; Joseph M. Okoh

2002-01-31T23:59:59.000Z

306

Mercury-Mercury Tunneling Junctions. 1. Electron Tunneling Across Symmetric and Asymmetric Alkanethiolate Bilayers  

E-Print Network [OSTI]

Mercury-Mercury Tunneling Junctions. 1. Electron Tunneling Across Symmetric and Asymmetric by bringing in contact two small (3 ? 10-3 cm2) mercury drop electrodes in a 5-20% (v/v) hexadecane solution incorporating alkanethiolate-type monolayer films. The results reported below convince us that the mercury

Majda, Marcin

307

Assessment of mercury emissions from the Afton copper smelter, British Columbia, Canada  

SciTech Connect (OSTI)

The afton Copper Smelter adjacent to Kamloops, British Columbia, Canada commenced operation in 1978 and employed a mercury scrubbing system. Two years of preproduction studies, which included monitoring for mercury in ambient air, water, soil, and vegetation were performed. The results from similar studies conducted during four full years (1978-81) and two partial years (1982-83) of production are presented in the data analysis. These programs illustrated that the most frequent ground impingement occurred within a 1.6-3.2-km radius of the source, and that the levels decreased with increasing distance from the source to a maximum radius of 8 km. The results of a comprehensive source monitoring program illustrated that the average mercury emission levels ranged from 3.2 to 6.8 kg/calendar day during 1979-81, and that the majority of the emissions were in a vapor form. The ambient monitoring data acquired when smelter operations were significantly reduced indicate a quick recovery to preproduction levels in virtually all monitored parameters and at most monitored sites. The integrated results from all mercury monitoring programs illustrate the environmental impact from mercury emissions which were two to four times the permit standard of 1.8 kg/day.

Robertson, J.D.; Price, C.J.

1986-07-01T23:59:59.000Z

308

Organic vapor jet printing system  

DOE Patents [OSTI]

An organic vapor jet printing system includes a pump for increasing the pressure of an organic flux.

Forrest, Stephen R

2012-10-23T23:59:59.000Z

309

Large-Scale Mercury Control Technology Testing for Lignite-Fired Utilities - Oxidation Systems for Wet FGD  

SciTech Connect (OSTI)

Mercury (Hg) control technologies were evaluated at Minnkota Power Cooperative's Milton R. Young (MRY) Station Unit 2, a 450-MW lignite-fired cyclone unit near Center, North Dakota, and TXU Energy's Monticello Steam Electric Station (MoSES) Unit 3, a 793-MW lignite--Powder River Basin (PRB) subbituminous coal-fired unit near Mt. Pleasant, Texas. A cold-side electrostatic precipitator (ESP) and wet flue gas desulfurization (FGD) scrubber are used at MRY and MoSES for controlling particulate and sulfur dioxide (SO{sub 2}) emissions, respectively. Several approaches for significantly and cost-effectively oxidizing elemental mercury (Hg{sup 0}) in lignite combustion flue gases, followed by capture in an ESP and/or FGD scrubber were evaluated. The project team involved in performing the technical aspects of the project included Babcock & Wilcox, the Energy & Environmental Research Center (EERC), the Electric Power Research Institute, and URS Corporation. Calcium bromide (CaBr{sub 2}), calcium chloride (CaCl{sub 2}), magnesium chloride (MgCl{sub 2}), and a proprietary sorbent enhancement additive (SEA), hereafter referred to as SEA2, were added to the lignite feeds to enhance Hg capture in the ESP and/or wet FGD. In addition, powdered activated carbon (PAC) was injected upstream of the ESP at MRY Unit 2. The work involved establishing Hg concentrations and removal rates across existing ESP and FGD units, determining costs associated with a given Hg removal efficiency, quantifying the balance-of-plant impacts of the control technologies, and facilitating technology commercialization. The primary project goal was to achieve ESP-FGD Hg removal efficiencies of {ge}55% at MRY and MoSES for about a month.

Steven A. Benson; Michael J. Holmes; Donald P. McCollor; Jill M. Mackenzie; Charlene R. Crocker; Lingbu Kong; Kevin C. Galbreath

2007-03-31T23:59:59.000Z

310

FULL-SCALE TESTING OF ENHANCED MERCURY CONTROL TECHNOLOGIES FOR WET FGD SYSTEMS  

SciTech Connect (OSTI)

Wet flue gas desulfurization (wet FGD) systems are currently installed on about 25% of the coal-fired utility generating capacity in the U.S., representing about 15% of the number of coal-fired units. Depending on the effect of operating parameters such as mercury content of the coal, form of mercury (elemental or oxidized) in the flue gas, scrubber spray tower configuration, liquid-to-gas ratio, and slurry chemistry, FGD systems can provide cost-effective, near-term mercury emissions control options with a proven history of commercial operation. For boilers already equipped with FGD systems, the incremental cost of any vapor phase mercury removal achieved is minimal. To be widely accepted and implemented, technical approaches that improve mercury removal performance for wet FGD systems should also have low incremental costs and have little or no impact on operation and SO{sub 2} removal performance. The ultimate goal of the Full-scale Testing of Enhanced Mercury Control for Wet FGD Systems Program was to commercialize methods for the control of mercury in coal-fired electric utility systems equipped with wet flue gas desulfurization (wet FGD). The program was funded by the U.S. Department of Energy's National Energy Technology Laboratory, the Ohio Coal Development Office within the Ohio Department of Development, and Babcock & Wilcox. Host sites and associated support were provided by Michigan South Central Power Agency (MSCPA) and Cinergy. Field-testing was completed at two commercial coal-fired utilities with wet FGD systems: (1) MSCPA's 55 MW{sub e} Endicott Station and (2) Cinergy's 1300 MW{sub e} Zimmer Station. Testing was conducted at these two locations because of the large differences in size and wet scrubber chemistry. Endicott employs a limestone, forced oxidation (LSFO) wet FGD system, whereas Zimmer uses Thiosorbic{reg_sign} Lime (magnesium enhanced lime) and ex situ oxidation. Both locations burn Ohio bituminous coal.

D.K. McDonald; G.T. Amrhein; G.A. Kudlac; D. Madden Yurchison

2003-05-07T23:59:59.000Z

311

Method and apparatus for monitoring the flow of mercury in a system  

DOE Patents [OSTI]

An apparatus and method for monitoring the flow of mercury in a system are disclosed. The equipment enables the entrainment of the mercury in a carrier gas e.g., an inert gas, which passes as mercury vapor between a pair of optically transparent windows. The attenuation of the emission is indicative of the quantity of mercury (and its isotopes) in the system. A 253.7 nm light is shone through one of the windows and the unabsorbed light is detected through the other window. The absorption of the 253.7 nm light is thereby measured whereby the quantity of mercury passing between the windows can be determined. The apparatus includes an in-line sensor for measuring the quantity of mercury. It includes a conduit together with a pair of apertures disposed in a face to face relationship and arranged on opposite sides of the conduit. A pair of optically transparent windows are disposed upon a pair of viewing tubes. A portion of each of the tubes is disposed inside of the conduit and within each of the apertures. The two windows are disposed in a face to face relationship on the ends of the viewing tubes and the entire assembly is hermetically sealed from the atmosphere whereby when 253.7 nm ultraviolet light is shone through one of the windows and detected through the other, the quantity of mercury which is passing by can be continuously monitored due to absorption which is indicated by attenuation of the amplitude of the observed emission. 4 figs.

Grossman, M.W.

1987-12-15T23:59:59.000Z

312

Mercury switch with non-wettable electrodes  

DOE Patents [OSTI]

A mercury switch device comprising a pool of mercury and a plurality of electrical contacts made of or coated with a non-wettable material such as titanium diboride.

Karnowsky, Maurice M. (Albulquerque, NM); Yost, Frederick G. (Carlsbad, NM)

1987-01-01T23:59:59.000Z

313

Nested-grid simulation of mercury over North America  

E-Print Network [OSTI]

coal combustion, waste incineration and gold mining (Streetsprofiles for waste incineration (22 % Hg(0), 78 % Hg(II)).

2012-01-01T23:59:59.000Z

314

OXIDATION OF MERCURY ACROSS SCR CATALYSTS IN COAL-FIRED POWER PLANTS BURNING LOW RANK FUELS  

SciTech Connect (OSTI)

The objectives of this program were to measure the oxidation of mercury in flue gas across SCR catalyst in a coal-fired power plant burning low rank fuels using a slipstream reactor containing multiple commercial catalysts in parallel and to develop a greater understanding of mercury oxidation across SCR catalysts in the form of a simple model. The Electric Power Research Institute (EPRI) and Argillon GmbH provided co-funding for this program. REI used a multicatalyst slipstream reactor to determine oxidation of mercury across five commercial SCR catalysts at a power plant that burned a blend of 87% subbituminous coal and 13% bituminous coal. The chlorine content of the blend was 100 to 240 {micro}g/g on a dry basis. Mercury measurements were carried out when the catalysts were relatively new, corresponding to about 300 hours of operation and again after 2,200 hours of operation. NO{sub x}, O{sub 2} and gaseous mercury speciation at the inlet and at the outlet of each catalyst chamber were measured. In general, the catalysts all appeared capable of achieving about 90% NO{sub x} reduction at a space velocity of 3,000 hr{sup -1} when new, which is typical of full-scale installations; after 2,200 hours exposure to flue gas, some of the catalysts appeared to lose NO{sub x} activity. For the fresh commercial catalysts, oxidation of mercury was in the range of 25% to 65% at typical full-scale space velocities. A blank monolith showed no oxidation of mercury under any conditions. All catalysts showed higher mercury oxidation without ammonia, consistent with full-scale measurements. After exposure to flue gas for 2,200 hours, some of the catalysts showed reduced levels of mercury oxidation relative to the initial levels of oxidation. A model of Hg oxidation across SCRs was formulated based on full-scale data. The model took into account the effects of temperature, space velocity, catalyst type and HCl concentration in the flue gas.

Constance Senior

2004-12-31T23:59:59.000Z

315

Enthalpies of Vaporization and Vapor Pressures of Some Deuterated Hydrocarbons. Liquid-Vapor Pressure Isotope Effects  

E-Print Network [OSTI]

* Department of Chemistry and Biochemistry, University of MissourisSt. Louis, St. Louis, Missouri 63121 Liquid vapor pressure isotope effects have generally been observed, pD > pH.12 Vapor pressure and sublimation

Chickos, James S.

316

Final technical report; Mercury Release from Organic matter (OM) and OM-Coated Mineral Surfaces  

SciTech Connect (OSTI)

This document is the final technical report for a project designed to address fundamental processes controlling the release of mercury from flood plain soils associated with East Fork Poplar Creek, Tennessee near the U.S. Department of Energy Oak Ridge facility. The report summarizes the activities, findings, presentations, and publications resulting from an award to the U.S. Geological that were part of a larger overall effort including Kathy Nagy (University of Illinois, Chicago, Ill) and Joseph Ryan (University of Colorado, Boulder, CO). The specific charge for the U.S.G.S. portion of the study was to provide analytical support for the larger group effort (Nagy and Ryan), especially with regard to analyses of Hg and dissolved organic matter, and to provide information about the release of mercury from the floodplain soils.

Aiken, George

2014-10-02T23:59:59.000Z

317

Mercury bioaccumulation in Lavaca Bay, Texas  

E-Print Network [OSTI]

(waves), and human activities (dredging and shrimping) can potentially release mercury to the overlying water (LINDBERG and HARRISS, 1977; CRANSTON, 1976). The solubility, reactivity, and toxicity of mercury is dependent on its form. Divalent mercury... MERCURY BIOACCUMULATION IN LAVACA BAY, TEXAS A Thesis by SALLY JO PALMER Submitted to the Office of Graduate Studies of Texas ABM University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE August 1992 Major...

Palmer, Sally Jo

1992-01-01T23:59:59.000Z

318

Release of Ammonium and Mercury from NOx Controlled Fly Ash  

SciTech Connect (OSTI)

One of the goals of the Department of Energy is to increase the reuse of coal utilization byproducts (CUB) to 50% by 2010. This will require both developing new markets and maintaining traditional ones such as the use of fly ash in concrete. However, the addition of pollution control devices can introduce side-effects that affect the marketability of the CUB. Such can be the case when NOx control is achieved using selective catalytic or non-catalytic reduction (SCR or SNCR). Depending on site-specific details, the ammonia slip can cause elevated levels of NH3 in the fly ash. Disposal of ammoniated fly ash can present environmental concerns related to the amount of ammonia that might be released, the amount of water that might become contaminated, and the extent to which metals might be mobilized by the presence of the ammonia. Ammonia retained in fly ash appears to be present as either an ammonium salt or as a chemisorbed species. Mercury in the leachates correlated to neither the amount of leachable ammonium nor to the total amount of Hg in the ash. The strongest correlation was between the decreases in the amount of Hg leached with increased LOI.

Schroeder, K.T.; Cardone, C.R.; Kim, A.G

2007-07-01T23:59:59.000Z

319

2003 Mercury Computer Systems, Inc. Data Reorganization  

E-Print Network [OSTI]

© 2003 Mercury Computer Systems, Inc. Data Reorganization Interface (DRI) Data Reorganization Interface (DRI) Kenneth Cain Jr. Mercury Computer Systems, Inc. High Performance Embedded Computing (HPEC Mercury Computer Systems, Inc. Status update for the DRI-1.0 standard since Sep. 2002 publication Outline

Kepner, Jeremy

320

3, 35253541, 2003 Modelling of Mercury  

E-Print Network [OSTI]

ACPD 3, 3525­3541, 2003 Modelling of Mercury with the Danish Eulerian Hemispheric Model J. H and Physics Discussions Modelling of mercury with the Danish Eulerian Hemispheric Model J. H. Christensen, J Correspondence to: J. H. Christensen (jc@dmu.dk) 3525 #12;ACPD 3, 3525­3541, 2003 Modelling of Mercury

Paris-Sud XI, Université de

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321

Atmospheric Chemistry, Modeling, and Biogeochemistry of Mercury  

E-Print Network [OSTI]

Atmospheric Chemistry, Modeling, and Biogeochemistry of Mercury Noelle Eckley Selin *Reprinted from Mercury in the Environment: Pattern and Process (Chapter 5) pp. 73-80 Copyright © 2012 with kind, and Biogeochemistry of Mercury NOELLE ECKLEY SELIN and their distribution in the atmosphere. This includes

322

Mercury: Recovering Forgotten Passwords Using Personal Devices  

E-Print Network [OSTI]

Mercury: Recovering Forgotten Passwords Using Personal Devices Mohammad Mannan1 , David Barrera2, and to allow forgotten passwords to be securely restored, we present a scheme called Mercury. Its primary mode and revealed to the user. A prototype implementation of Mercury is available as an Android application. 1

Van Oorschot, Paul

323

2003 Mercury Computer Systems, Inc. Delivered Performance  

E-Print Network [OSTI]

© 2003 Mercury Computer Systems, Inc. Delivered Performance Predictions and Trends for RISC Applications Luke Cico (lcico@mc.com) Mark Merritt (mmerritt@mc.com) Mercury Computer Systems, Inc. Chelmsford, MA 01824 #12;© 2003 Mercury Computer Systems, Inc. Goals of PresentationGoals of Presentation

Kepner, Jeremy

324

REPLACE YOUR MERCURY THERMOMETERS BEFORE THEY BREAK!  

E-Print Network [OSTI]

REPLACE YOUR MERCURY THERMOMETERS BEFORE THEY BREAK! Did you know, mercury from broken thermometers to the local environment, if broken thermometers in sinks eventually end at the sanitary sewer plant. Broken mercury thermometers create hazardous waste that is costly to clean up and costly to dispose of. Other

325

Interactive toxicity of inorganic mercury and trichloroethylene in rat and human proximal tubules: Effects on apoptosis, necrosis, and glutathione status  

SciTech Connect (OSTI)

Simultaneous or prior exposure to one chemical may alter the concurrent or subsequent response to another chemical, often in unexpected ways. This is particularly true when the two chemicals share common mechanisms of action. The present study uses the paradigm of prior exposure to study the interactive toxicity between inorganic mercury (Hg{sup 2+}) and trichloroethylene (TRI) or its metabolite S-(1,2-dichlorovinyl)-L-cysteine (DCVC) in rat and human proximal tubule. Pretreatment of rats with a subtoxic dose of Hg{sup 2+} increased expression of glutathione S-transferase-{alpha}1 (GST{alpha}1) but decreased expression of GST{alpha}2, increased activities of several GSH-dependent enzymes, and increased GSH conjugation of TRI. Primary cultures of rat proximal tubular (rPT) cells exhibited both necrosis and apoptosis after incubation with Hg{sup 2+}. Pretreatment of human proximal tubular (hPT) cells with Hg{sup 2+} caused little or no changes in GST expression or activities of GSH-dependent enzymes, decreased apoptosis induced by TRI or DCVC, but increased necrosis induced by DCVC. In contrast, pretreatment of hPT cells with TRI or DCVC protected from Hg{sup 2+} by decreasing necrosis and increasing apoptosis. Thus, whereas pretreatment of hPT cells with Hg{sup 2+} exacerbated cellular injury due to TRI or DCVC by shifting the response from apoptosis to necrosis, pretreatment of hPT cells with either TRI or DCVC protected from Hg{sup 2+}-induced cytotoxicity by shifting the response from necrosis to apoptosis. These results demonstrate that by altering processes related to GSH status, susceptibilities of rPT and hPT cells to acute injury from Hg{sup 2+}, TRI, or DCVC are markedly altered by prior exposures.

Lash, Lawrence H. [Department of Pharmacology, Wayne State University School of Medicine, 540 East Canfield Avenue, Detroit, MI 48201 (United States)]. E-mail: l.h.lash@wayne.edu; Putt, David A. [Department of Pharmacology, Wayne State University School of Medicine, 540 East Canfield Avenue, Detroit, MI 48201 (United States); Hueni, Sarah E. [Department of Pharmacology, Wayne State University School of Medicine, 540 East Canfield Avenue, Detroit, MI 48201 (United States); Payton, Scott G. [Department of Pharmacology, Wayne State University School of Medicine, 540 East Canfield Avenue, Detroit, MI 48201 (United States); Zwickl, Joshua [Department of Pharmacology, Wayne State University School of Medicine, 540 East Canfield Avenue, Detroit, MI 48201 (United States)

2007-06-15T23:59:59.000Z

326

CHARACTERIZATION OF COAL COMBUSTION BY-PRODUCTS FOR THE RE-EVOLUTION OF MERCURY INTO ECOSYSTEMS  

SciTech Connect (OSTI)

There is concern that mercury (Hg) in coal combustion by-products might be emitted into the environment during processing to other products or after the disposal/landfill of these by-products. This perception may limit the opportunities to use coal combustion by-products in recycle/reuse applications and may result in additional, costly disposal regulations. In this program, CONSOL conducted a comprehensive sampling and analytical program to include ash, flue gas desulfurization (FGD) sludge, and coal combustion by-products. This work is necessary to help identify potential problems and solutions important to energy production from fossil fuels. The program objective was to evaluate the potential for mercury emissions by leaching or volatilization, to determine if mercury enters the water surrounding an active FGD disposal site and an active fly ash slurry impoundment site, and to provide data that will allow a scientific assessment of the issue. Toxicity Characteristic Leaching Procedure (TCLP) test results showed that mercury did not leach from coal, bottom ash, fly ash, spray dryer/fabric filter ash or forced oxidation gypsum (FOG) in amounts leading to concentrations greater than the detection limit of the TCLP method (1.0 ng/mL). Mercury was detected at very low concentrations in acidic leachates from all of the fixated and more than half of the unfixated FGD sludge samples, and one of the synthetic aggregate samples. Mercury was not detected in leachates from any sample when deionized water (DI water) was the leaching solution. Mercury did not leach from electrostatic precipitator (ESP) fly ash samples collected during activated carbon injection for mercury control in amounts greater than the detection limit of the TCLP method (1.0 ng/mL). Volatilization tests could not detect mercury loss from fly ash, spray dryer/fabric filter ash, unfixated FGD sludge, or forced oxidation gypsum; the mercury concentration of these samples all increased, possibly due to absorption from ambient surroundings. Mercury loss of 18-26% was detected after 3 and 6 months at 100 F and 140 F from samples of the fixated FGD sludge. Water samples were collected from existing ground water monitoring wells around an active FGD disposal site (8 wells) and an active fly ash slurry impoundment (14 wells). These were wells that the plants have installed to comply with ground water monitoring requirements of their permits. Mercury was not detected in any of the water samples collected from monitoring wells at either site. A literature review concluded that coal combustion byproducts can be disposed of in properly designed landfills that minimize the potentially negative impacts of water intrusion that carries dissolved organic matter (DOM). Dissolved organic matter and sulfate-reducing bacteria can promote the transformation of elemental or oxidized mercury into methyl mercury. The landfill should be properly designed and capped with clays or similar materials to minimize the wet-dry cycles that promote the release of methylmercury.

J.A. Withum; J.E. Locke; S.C. Tseng

2005-03-01T23:59:59.000Z

327

Lead, mercury, and cadmium exposure and attention deficit hyperactivity disorder in children  

SciTech Connect (OSTI)

Background: There is limited research examining the relationship between lead (Pb) exposure and medically diagnosed attention deficit hyperactivity disorder (ADHD) in children. The role of mercury (Hg) and cadmium (Cd) exposures in ADHD development is even less clear. Objectives: To examine the relationship between Pb, Hg, and Cd and ADHD in children living inside and outside a Lead Investigation Area (LIA) of a former lead refinery in Omaha, NE. Methods: We carried out a case-control study with 71 currently medically diagnosed ADHD cases and 58 controls from a psychiatric clinic and a pediatric clinic inside and outside of the LIA. The participants were matched on age group (58, 912 years), sex, race (African American or Caucasians and others), and location (inside or outside LIA). We measured whole blood Pb, total Hg, and Cd using inductively coupled plasma mass spectrometry. Results: Inside the LIA, the 27 cases had blood Pb geometric mean (GM) 1.89 g/dL and the 41 controls had 1.51 g/dL. Outside the LIA, the 44 cases had blood Pb GM 1.02 g/dL while the 17 controls had 0.97 g/dL. After adjustment for matching variables and maternal smoking, socioeconomic status, and environmental tobacco exposure, each natural log unit blood Pb had an odds ratio of 2.52 with 95% confidence interval of 1.075.92. Stratification by the LIA indicated similar point estimate but wider CIs. No associations were observed for Hg or Cd. Conclusions: Postnatal Pb exposure may be associated with higher risk of clinical ADHD, but not the postnatal exposure to Hg or Cd. -- Highlights: Blood Pb levels are associated with ADHD diagnosis in children. No association was found between blood Cd or Hg levels and ADHD. Children living close to hazardous waste site need to reduce metal exposure.

Kim, Stephani [Division of Epidemiology and Biostatistics, Department of Environmental Health, University of Cincinnati College of Medicine, Cincinnati, OH 45267 (United States)] [Division of Epidemiology and Biostatistics, Department of Environmental Health, University of Cincinnati College of Medicine, Cincinnati, OH 45267 (United States); Arora, Monica [Department of Psychiatry, Creighton University School of Medicine, Omaha, NE 68131 (United States)] [Department of Psychiatry, Creighton University School of Medicine, Omaha, NE 68131 (United States); Fernandez, Cristina [Department of Pediatrics, Creighton University School of Medicine, Omaha, NE 68131 (United States)] [Department of Pediatrics, Creighton University School of Medicine, Omaha, NE 68131 (United States); Landero, Julio; Caruso, Joseph [Metallomics Center, Department of Chemistry, University of Cincinnati, Cincinnati, OH 45221 (United States)] [Metallomics Center, Department of Chemistry, University of Cincinnati, Cincinnati, OH 45221 (United States); Chen, Aimin, E-mail: aimin.chen@uc.edu [Division of Epidemiology and Biostatistics, Department of Environmental Health, University of Cincinnati College of Medicine, Cincinnati, OH 45267 (United States)] [Division of Epidemiology and Biostatistics, Department of Environmental Health, University of Cincinnati College of Medicine, Cincinnati, OH 45267 (United States)

2013-10-15T23:59:59.000Z

328

Stratified vapor generator  

DOE Patents [OSTI]

A stratified vapor generator (110) comprises a first heating section (H.sub.1) and a second heating section (H.sub.2). The first and second heating sections (H.sub.1, H.sub.2) are arranged so that the inlet of the second heating section (H.sub.2) is operatively associated with the outlet of the first heating section (H.sub.1). A moisture separator (126) having a vapor outlet (164) and a liquid outlet (144) is operatively associated with the outlet (124) of the second heating section (H.sub.2). A cooling section (C.sub.1) is operatively associated with the liquid outlet (144) of the moisture separator (126) and includes an outlet that is operatively associated with the inlet of the second heating section (H.sub.2).

Bharathan, Desikan (Lakewood, CO); Hassani, Vahab (Golden, CO)

2008-05-20T23:59:59.000Z

329

ARM - Water Vapor  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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330

VAPOR PRESSURES AND HEATS OF VAPORIZATION OF PRIMARY COAL TARS  

SciTech Connect (OSTI)

This project had as its main focus the determination of vapor pressures of coal pyrolysis tars. It involved performing measurements of these vapor pressures and from them, developing vapor pressure correlations suitable for use in advanced pyrolysis models (those models which explicitly account for mass transport limitations). This report is divided into five main chapters. Each chapter is a relatively stand-alone section. Chapter A reviews the general nature of coal tars and gives a summary of existing vapor pressure correlations for coal tars and model compounds. Chapter B summarizes the main experimental approaches for coal tar preparation and characterization which have been used throughout the project. Chapter C is concerned with the selection of the model compounds for coal pyrolysis tars and reviews the data available to us on the vapor pressures of high boiling point aromatic compounds. This chapter also deals with the question of identifying factors that govern the vapor pressures of coal tar model materials and their mixtures. Chapter D covers the vapor pressures and heats of vaporization of primary cellulose tars. Chapter E discusses the results of the main focus of this study. In summary, this work provides improved understanding of the volatility of coal and cellulose pyrolysis tars. It has resulted in new experimentally verified vapor pressure correlations for use in pyrolysis models. Further research on this topic should aim at developing general vapor pressure correlations for all coal tars, based on their molecular weight together with certain specific chemical characteristics i.e. hydroxyl group content.

Eric M. Suuberg; Vahur Oja

1997-07-01T23:59:59.000Z

331

Mercury Delivery System Tony Gabriel, Phil Spampinato  

E-Print Network [OSTI]

Concept Hydraulic Fluid Cylinder (3000 psi) Hg Cylinder (1000 psi) Hg Discharge Hg Inlet #12;6 OAK RIDGE losses isolated to hydraulic system - Flow losses identical to those in pump system #12;8 OAK RIDGE Motor 20 20 hp * 5% inefficiency 1 19 42 42 1 1 Hyd Pump energy performed on piston = press

McDonald, Kirk

332

MERCURY REMOVAL IN A NON-THERMAL, PLASMA-BASED MULTI-POLLUTANT CONTROL TECHNOLOGY FOR UTILITY BOILERS  

SciTech Connect (OSTI)

Powerspan has conducted pilot scale testing of a multi-pollutant control technology at FirstEnergy's Burger Power Plant under a cooperative agreement with the U.S. Department of Energy. The technology, Electro-Catalytic Oxidation (ECO), simultaneously removes sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), fine particulate matter (PM{sub 2.5}) and mercury (Hg) from the flue gas of coal-fired power plants. Powerspan's ECO{reg_sign} pilot test program focused on optimization of Hg removal in a 1-MWe slipstream pilot while maintaining greater than 90% removal of NO{sub x} and 98% removal of SO{sub 2}. This Final Technical Report discusses pilot operations, installation and maintenance of the Hg SCEMS instrumentation, and performance results including component and overall removal efficiencies of SO{sub 2}, NO{sub x}, PM and Hg from the flue gas and removal of captured Hg from the co-product fertilizer stream.

Christopher R. McLaron

2004-12-01T23:59:59.000Z

333

DEVELOPMENT AND SELECTION OF TECHNOLOGIES FOR MERCURY MANAGEMENT ON U.S. DEPARTMENT OF ENERGY SITES: THE MER01-MER04 AND MERCURY SPECIATION DEMONSTRATIONS  

SciTech Connect (OSTI)

The U.S. Department of Energy's (DOE's) Transuranic and Mixed Waste Focus Area (TMFA), funded from fiscal year (FY) 1996 though FY 2002, was tasked with finding solutions for the mixed waste treatment problems of the DOE complex. During TMFA's initial technical baseline development process, three of the top four technology deficiencies identified were the need for amalgamation, stabilization, and separation/removal technologies for the treatment of mercury-contaminated mixed waste. The Mercury Working Group (HgWG), a selected group of representatives from DOE sites with significant mercury waste inventories, assisted TMFA in soliciting, identifying, initiating, and managing efforts to address these areas. Solicitations and contract awards were made to the private sector to demonstrate both the amalgamation and stabilization processes using both actual mixed wastes and surrogate samples. The goal was to develop separation and removal processes that will meet DOE's needs. This paper discusses the technology selection process, development activities, and the accomplishments of TMFA through these various activities.

Morris, Michael I.; Hulet, Greg A.

2003-02-27T23:59:59.000Z

334

ARM Water Vapor IOP  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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335

Water Vapor Experiment Concludes  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear SecurityTensile Strain Switched FerromagnetismWaste and Materials Disposition3 Water Vapor Experiment Concludes The

336

To estimate vapor pressure easily  

SciTech Connect (OSTI)

Vapor pressures as functions of temperature for approximately 700 major organic chemical compounds are given. The tabulation also gives the temperature range for which the data are applicable. Minimum and maximum temperatures are denoted by TMIN and TMAX. The Antoine equation that correlates vapor pressure as a function of temperature is described. A representative comparison of calculated and actual data values for vapor pressure is shown for ethyl alcohol. The coefficient tabulation is based on both literature (experimental data) and estimated values.

Yaws, C.L.; Yang, H.C. (Lamar Univ., Beaumont, TX (USA))

1989-10-01T23:59:59.000Z

337

Vaporization of zinc from scrap  

SciTech Connect (OSTI)

The rate of zinc vaporization from galvanized scrap was measured using a thermogravimetric apparatus along with chemical analysis. It is found that the rate of zinc vaporization is very fast in nitrogen and carbon monoxide atmospheres at temperatures higher than 950 C. At lower temperature rate decreases with decreasing temperature and is controlled by the gas phase mass transport. The simultaneous oxidation and vaporization of zinc occurs when the samples were heated in carbon dioxide and air. The current experimental results indicate that almost all of the zinc from scrap vaporizes during the heating process in a very short period of time after the temperature reaches above 850 C.

Ozturk, B.; Fruehan, R.J. [Carnegie Mellon Univ., Pittsburgh, PA (United States)

1996-12-31T23:59:59.000Z

338

A Mercury orientation model including non-zero obliquity and librations  

E-Print Network [OSTI]

Long-period forcing of Mercurys libration in longitude.M. : Resonant forcing of Mercurys libration in longitude.A revised control network for Mercury. J. Geophys. Res. 104,

Margot, Jean-Luc

2009-01-01T23:59:59.000Z

339

Vapor spill pipe monitor  

DOE Patents [OSTI]

The invention is a method and apparatus for continually monitoring the composition of liquefied natural gas flowing from a spill pipe during a spill test by continually removing a sample of the LNG by means of a probe, gasifying the LNG in the probe, and sending the vaporized LNG to a remote ir gas detector for analysis. The probe comprises three spaced concentric tubes surrounded by a water jacket which communicates with a flow channel defined between the inner and middle, and middle and outer tubes. The inner tube is connected to a pump for providing suction, and the probe is positioned in the LNG flow below the spill pipe with the tip oriented partly downward so that LNG is continuously drawn into the inner tube through a small orifice. The probe is made of a high thermal conductivity metal. Hot water is flowed through the water jacket and through the flow channel between the three tubes to provide the necessary heat transfer to flash vaporize the LNG passing through the inner channel of the probe. The gasified LNG is transported through a connected hose or tubing extending from the probe to a remote ir sensor which measures the gas composition.

Bianchini, G.M.; McRae, T.G.

1983-06-23T23:59:59.000Z

340

Mercury-Contaminated Hydraulic Mining Debris in San Francisco Bay  

E-Print Network [OSTI]

S, and Flegal AR 2008. Mercury in the San Francisco Estuary.may 2010 Mercury-Contaminated Hydraulic Mining Debris in Sancontaminants such as ele- mental mercury and cyanide used in

Bouse, Robin M; Fuller, Christopher C; Luoma, Sam; Hornberger, Michelle I; Jaffe, Bruce E; Smith, Richard E

2010-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


341

Control of mercury methylation in wetlands through iron addition  

E-Print Network [OSTI]

Mason, R. P. ; Flegal, A. R. , Mercury speciation in the SanP. ; Flegal, A. R. , Decadal mercury trends in San FranciscoP. G. ; Nelson, D. C. , Mercury methylation from unexpected

Sedlak, David L; Ulrich, Patrick D

2009-01-01T23:59:59.000Z

342

Amended Silicated for Mercury Control  

SciTech Connect (OSTI)

Amended Silicates{trademark}, a powdered, noncarbon mercury-control sorbent, was tested at Duke Energy's Miami Fort Station, Unit 6 during the first quarter of 2006. Unit 6 is a 175-MW boiler with a cold-side electrostatic precipitator (ESP). The plant burns run-of-the-river eastern bituminous coal with typical ash contents ranging from 8-15% and sulfur contents from 1.6-2.6% on an as-received basis. The performance of the Amended Silicates sorbent was compared with that for powdered activated carbon (PAC). The trial began with a period of baseline monitoring during which no sorbent was injected. Sampling during this and subsequent periods indicated mercury capture by the native fly ash was less than 10%. After the baseline period, Amended Silicates sorbent was injected at several different ratios, followed by a 30-day trial at a fixed injection ratio of 5-6 lb/MMACF. After this period, PAC was injected to provide a comparison. Approximately 40% mercury control was achieved for both the Amended Silicates sorbent and PAC at injection ratios of 5-6 lbs/MMACF. Higher injection ratios did not achieve significantly increased removal. Similar removal efficiencies have been reported for PAC injection trials at other plants with cold-side ESPs, most notably for plants using medium to high sulfur coal. Sorbent injection did not detrimentally impact plant operations and testing confirmed that the use of Amended Silicates sorbent does not degrade fly ash quality (unlike PAC). The cost for mercury control using either PAC or Amended Silicates sorbent was estimated to be equivalent if fly ash sales are not a consideration. However, if the plant did sell fly ash, the effective cost for mercury control could more than double if those sales were no longer possible, due to lost by-product sales and additional cost for waste disposal. Accordingly, the use of Amended Silicates sorbent could reduce the overall cost of mercury control by 50% or more versus PAC for locations where fly ash is sold as a by-product.

James Butz; Thomas Broderick; Craig Turchi

2006-12-31T23:59:59.000Z

343

Remediation of Mercury and Industrial Contaminants Applied Field...  

Office of Environmental Management (EM)

Remediation of Mercury and Industrial Contaminants Applied Field Research Initiative (RoMIC-AFRI) Remediation of Mercury and Industrial Contaminants Applied Field Research...

344

Mercury/Waterfilling: Optimum Power Allocation with Arbitrary Input Constellations  

E-Print Network [OSTI]

Mercury/Waterfilling: Optimum Power Allocation with Arbitrary Input Constellations Angel Lozano gives the power allocation policy, referred to as mercury/waterfilling, that maximizes the sum mutual

Verdú, Sergio

345

Process for removing mercury from aqueous solutions  

DOE Patents [OSTI]

A process for removing mercury from water to a level not greater than two parts per billion wherein an anion exchange material that is insoluble in water is contacted first with a sulfide containing compound and second with a compound containing a bivalent metal ion forming an insoluble metal sulfide. To this treated exchange material is contacted water containing mercury. The water containing not more than two parts per billion of mercury is separated from the exchange material.

Googin, J.M.; Napier, J.M.; Makarewicz, M.A.; Meredith, P.F.

1985-03-04T23:59:59.000Z

346

Process for removing mercury from aqueous solutions  

DOE Patents [OSTI]

A process for removing mercury from water to a level not greater than two parts per billion wherein an anion exchange material that is insoluble in water is contacted first with a sulfide containing compound and second with a compound containing a bivalent metal ion forming an insoluble metal sulfide. To this treated exchange material is contacted water containing mercury. The water containing not more than two parts per billion of mercury is separated from the exchange material.

Googin, John M. (Oak Ridge, TN); Napier, John M. (Oak Ridge, TN); Makarewicz, Mark A. (Knoxville, TN); Meredith, Paul F. (Knoxville, TN)

1986-01-01T23:59:59.000Z

347

Active transport, substrate specificity, and methylation of Hg(II) in anaerobic bacteria  

SciTech Connect (OSTI)

The formation of methylmercury (MeHg), which is biomagnified in aquatic food chains and poses a risk to human health, is effected by some iron- and sulfate-reducing bacteria (FeRB and SRB) in anaerobic environments. However, very little is known regarding the mechanism of uptake of inorganic Hg by these organisms, in part because of the inherent difficulty in measuring the intracellular Hg concentration. By using the FeRB Geobacter sulfurreducens and the SRB Desulfovibrio desulfuricans ND132 as model organisms, we demonstrate that Hg(II) uptake occurs by active transport. We also establish that Hg(II) uptake by G. sulfurreducens is highly dependent on the characteristics of the thiols that bind Hg(II) in the external medium, with some thiols promoting uptake and methylation and others inhibiting both. The Hg(II) uptake system of D. desulfuricans has a higher affinity than that of G. sulfurreducens and promotes Hg methylation in the presence of stronger complexing thiols. We observed a tight coupling between Hg methylation and MeHg export from the cell, suggesting that these two processes may serve to avoid the build up and toxicity of cellular Hg. Our results bring up the question of whether cellular Hg uptake is specific for Hg(II) or accidental, occurring via some essential metal importer. Our data also point at Hg(II) complexation by thiols as an important factor controlling Hg methylation in anaerobic environments.

Schasfer, Jeffra [Princeton University; Rocks, Sara [Princeton University; Zheng, Wang [ORNL; Liang, Liyuan [ORNL; Gu, Baohua [ORNL; Morel, Francois M [ORNL

2011-01-01T23:59:59.000Z

348

Fuel vapor control device  

SciTech Connect (OSTI)

A fuel vapor control device is described having a valve opening and closing a passage connecting a carburetor and a charcoal canister according to a predetermined temperature. A first coil spring formed by a ''shape memory effect'' alloy is provided to urge the valve to open the passage when the temperature is high. A second coil spring urges the valve to close the passage. A solenoid is provided to urge an armature against the valve to close the passage against the force of the first coil spring when the engine is running. The solenoid heats the first coil spring to generate a spring force therein when the engine is running. When the engine is turned off, the solenoid is deactivated, and the force of the first spring overcomes the force of the second spring to open the passage until such time as the temperature of the first spring drops below the predetermined temperature.

Ota, I.; Nishimura, Y.; Nishio, S.; Yogo, K.

1987-10-20T23:59:59.000Z

349

Simultaneous Removal of NOx and Mercury in Low Temperature Selective Catalytic and Adsorptive Reactor  

SciTech Connect (OSTI)

The results of a 18-month investigation to advance the development of a novel Low Temperature Selective Catalytic and Adsorptive Reactor (LTSCAR), for the simultaneous removal of NO{sub x} and mercury (elemental and oxidized) from flue gases in a single unit operation located downstream of the particulate collectors, are reported. In the proposed LTSCAR, NO{sub x} removal is in a traditional SCR mode but at low temperature, and, uniquely, using carbon monoxide as a reductant. The concomitant capture of mercury in the unit is achieved through the incorporation of a novel chelating adsorbent. As conceptualized, the LTSCAR will be located downstream of the particulate collectors (flue gas temperature 140-160 C) and will be similar in structure to a conventional SCR. That is, it will have 3-4 beds that are loaded with catalyst and adsorbent allowing staged replacement of catalyst and adsorbent as required. Various Mn/TiO{sub 2} SCR catalysts were synthesized and evaluated for their ability to reduce NO at low temperature using CO as the reductant. It has been shown that with a suitably tailored catalyst more than 65% NO conversion with 100% N{sub 2} selectivity can be achieved, even at a high space velocity (SV) of 50,000 h-1 and in the presence of 2 v% H{sub 2}O. Three adsorbents for oxidized mercury were developed in this project with thermal stability in the required range. Based on detailed evaluations of their characteristics, the mercaptopropyltrimethoxysilane (MPTS) adsorbent was found to be most promising for the capture of oxidized mercury. This adsorbent has been shown to be thermally stable to 200 C. Fixed-bed evaluations in the targeted temperature range demonstrated effective removal of oxidized mercury from simulated flue gas at very high capacity ({approx}>58 mg Hg/g adsorbent). Extension of the capability of the adsorbent to elemental mercury capture was pursued with two independent approaches: incorporation of a novel nano-layer on the surface of the chelating mercury adsorbent to achieve in situ oxidation on the adsorbent, and the use of a separate titania-supported manganese oxide catalyst upstream of the oxidized mercury adsorbent. Both approaches met with some success. It was demonstrated that the concept of in situ oxidation on the adsorbent is viable, but the future challenge is to raise the operating capacity beyond the achieved limit of 2.7 mg Hg/g adsorbent. With regard to the manganese dioxide catalyst, elemental mercury was very efficiently oxidized in the absence of sulfur dioxide. Adequate resistance to sulfur dioxide must be incorporated for the approach to be feasible in flue gas. A preliminary benefits analysis of the technology suggests significant potential economic and environmental advantages.

Neville G. Pinto; Panagiotis G. Smirniotis

2006-03-31T23:59:59.000Z

350

Partitioning and chemical speciation of mercury, arsenic, and selenium during inert gas oil shale retorting  

SciTech Connect (OSTI)

A Green River shale from Colorado and a New Albany shale from Kentucky were retorted in the Pacific Northwest Laboratory 6-kg bench-scale retort at 1 to 2C/min and at 10C/min to maximum temperatures of 500 and 750C under a nitrogen sweep gas. The product streams were analyzed using a variety of methods including Zeeman atomic aabsortion spectroscopy, microwave-induced helium plasma spectroscopy, x-ray fluorescence, instrumental neutron activation analysis, high-pressure liquid and silica gel column chromatography, and mercury cold vapor atomic absorption. The results obtained using these analytical methods indicate the the distribution of mercury, arsenic, and selenium in the product stream is a function of oil shale type, heating rates, and maximum retorting temperatures. 23 refs., 15 figs., 5 tabs.

Olsen, K.B.; Evans, J.C.; Sklarew, D.S.; Girvin, D.C.; Nelson, C.L.; Lepel, E.A.; Robertson, D.E.; Sanders, R.W.

1985-12-01T23:59:59.000Z

351

Crystal Growth And Characterization of the Model High-Temperature Superconductor HgBa{sub 2}CuO{sub 4+{delta}}  

SciTech Connect (OSTI)

Since the discovery of high-transition-temperature (T{sub c}) superconductivity in La{sub 2-x}Ba{sub x}CuO{sub 4} in 1986, the study of the lamellar copper oxides has remained at the forefront of condensed matter physics. Apart from their unusually high values of T{sub c}, these materials also exhibit a variety of complex phenomena and phases. This rich behavior is a consequence of the lamellar crystal structures, formed of copper-oxygen sheets separated by charge reservoir layers, and of the strong electron-electron correlations in the copper-oxygen sheets. After two decades of intensive research, which has stimulated many valuable new insights into correlated electron systems in general, there remains a lack of consensus regarding the correct theory for high-T{sub c} superconductivity. The ultimate technological goal of room-temperature superconductivity might only be attained after the development of a deeper understanding of the mercury-based compounds HgBa{sub 2}Ca{sub n-1}Cu{sub n}OI{sub 2n+2+{delta}}, which currently exhibit the highest T{sub c}values. One very important issue in this regard is the role of electronic versus chemical and structural inhomogeneities in these materials, and the associated need to separate material-specific properties from those that are essential to superconductivity. Unfortunately, there has been remarkably little scientific work on the mercury-based compounds because sizable crystals have not been available; quantitative measurements of any kind would be invaluable benchmarks for testing the theories of high-T{sub c} superconductivity. The compounds HgBa{sub 2}Ca{sub n-1}Cu{sub n}OI{sub 2n+2+{delta}} can be viewed as model systems not only because of their record high-T{sub c} values, but also because of their high-symmetry crystal structures. Of particular interest is the simplest member of this materials family, HgBa{sub 2}CuO{sub 4+{delta}} (Hg1201), which possesses only one copper-oxygen sheet per unit cell (n = 1), as shown schematically in Figure 1a. The largest crystals obtained by previous growth methods do not exceed 1 mm{sup 3}, and hence are insufficient in size for detailed studies by many experimental techniques. Here we report a novel recipe for the growth of Hg1201 crystals as well as detailed sample characterization results, including initial inelastic magnetic neutron scattering data. We note that samples grown by the method described here have already enabled recent optical conductivity, inelastic X-ray scattering, and angle-resolved photoemission studies.

Zhao, Xudong; Yu, Guichuan; Cho, Yong-Chan; Chabot-Couture, Guillaume; Barisic, Neven; Bourges, Philippe; Kaneko, Nobuhisa; Li, Yuan; Lu, Li; Motoyama, Eugene M.; Vajk,; Greven, Martin; /Stanford U., Appl. Phys. Dept. /SLAC, SSRL /Jilin U. /Stanford U., Phys. Dept. /Saclay /NIST, Wash., D.C.

2007-03-16T23:59:59.000Z

352

Mercury Geochemical, Groundwater Geochemical, And Radiometric...  

Open Energy Info (EERE)

Prospects In Northern Nevada Abstract Ground water sampling, desorbed mercury soil geochemical surveys and a radiometric geophysical survey was conducted in conjunction...

353

Alkaline sorbent injection for mercury control  

DOE Patents [OSTI]

A mercury removal system for removing mercury from combustion flue gases is provided in which alkaline sorbents at generally extremely low stoichiometric molar ratios of alkaline earth or an alkali metal to sulfur of less than 1.0 are injected into a power plant system at one or more locations to remove at least between about 40% and 60% of the mercury content from combustion flue gases. Small amounts of alkaline sorbents are injected into the flue gas stream at a relatively low rate. A particulate filter is used to remove mercury-containing particles downstream of each injection point used in the power plant system.

Madden, Deborah A. (Boardman, OH); Holmes, Michael J. (Washington Township, Stark County, OH)

2003-01-01T23:59:59.000Z

354

Alkaline sorbent injection for mercury control  

DOE Patents [OSTI]

A mercury removal system for removing mercury from combustion flue gases is provided in which alkaline sorbents at generally extremely low stoichiometric molar ratios of alkaline earth or an alkali metal to sulfur of less than 1.0 are injected into a power plant system at one or more locations to remove at least between about 40% and 60% of the mercury content from combustion flue gases. Small amounts of alkaline sorbents are injected into the flue gas stream at a relatively low rate. A particulate filter is used to remove mercury-containing particles downstream of each injection point used in the power plant system.

Madden, Deborah A. (Boardman, OH); Holmes, Michael J. (Washington Township, Stark County, OH)

2002-01-01T23:59:59.000Z

355

Mercury Sensing with Optically Responsive Gold Nanoparticles  

E-Print Network [OSTI]

1.1.5 Mercury detection Atomic absorption 19 and atomicsacrifices in simplicity. Atomic absorption or fluorescencedown to low nanogram masses. Atomic absorption/fluorescence

James, Jay Zachary

2012-01-01T23:59:59.000Z

356

Mercury concentrations in Maine sport fishes  

SciTech Connect (OSTI)

To assess mercury contamination of fish in Maine, fish were collected from 120 randomly selected lakes. The collection goal for each lake was five fish of the single most common sport fish species within the size range commonly harvested by anglers. Skinless, boneless fillets of fish from each lake were composited, homogenized, and analyzed for total mercury. The two most abundant species, brook trout Salvelinus fontinalis and smallmouth bass Micropterus dolomieu, were also analyzed individually. The composite fish analyses indicate high concentrations of mercury, particularly in large and long-lived nonsalmonid species. Chain pickerel Esox niger, smallmouth bass, largemouth bass Micropterus salmoides, and white perch Morone americana had the highest average mercury concentrations, and brook trout and yellow perch Perca flavescens had the lowest. The mean species composite mercury concentration was positively correlated with a factor incorporating the average size and age of the fish. Lakes containing fish with high mercury concentrations were not clustered near known industrial or population centers but were commonest in the area within 150 km of the seacoast, reflecting the geographical distribution of species that contained higher mercury concentrations. Stocked and wild brook trout were not different in length or weight, but wild fish were older and had higher mercury concentrations. Fish populations maintained by frequent introductions of hatchery-produced fish and subject to high angler exploitation rates may consist of younger fish with lower exposure to environmental mercury and thus contain lower concentrations than wild populations.

Stafford, C.P. [Univ. of Maine, Orono, ME (United States)] [Univ. of Maine, Orono, ME (United States); Haines, T.A. [Geological Survey, Orono, ME (United States)] [Geological Survey, Orono, ME (United States)

1997-01-01T23:59:59.000Z

357

Packed bed reactor for photochemical .sup.196 Hg isotope separation  

DOE Patents [OSTI]

Straight tubes and randomly oriented pieces of tubing having been employed in a photochemical mercury enrichment reactor and have been found to improve the enrichment factor (E) and utilization (U) compared to a non-packed reactor. One preferred embodiment of this system uses a moving bed (via gravity) for random packing.

Grossman, Mark W. (Belmont, MA); Speer, Richard (Reading, MA)

1992-01-01T23:59:59.000Z

358

Mercury Speciation in Coal-Fired Power Plant Flue Gas-Experimental Studies and Model Development  

SciTech Connect (OSTI)

The overall goal of the project was to obtain a fundamental understanding of the catalytic reactions that are promoted by solid surfaces present in coal combustion systems and develop a mathematical model that described key phenomena responsible for the fate of mercury in coal-combustion systems. This objective was achieved by carefully combining laboratory studies under realistic process conditions using simulated flue gas with mathematical modeling efforts. Laboratory-scale studies were performed to understand the fundamental aspects of chemical reactions between flue gas constituents and solid surfaces present in the fly ash and their impact on mercury speciation. Process models were developed to account for heterogeneous reactions because of the presence of fly ash as well as the deliberate addition of particles to promote Hg oxidation and adsorption. Quantum modeling was used to obtain estimates of the kinetics of heterogeneous reactions. Based on the initial findings of this study, additional work was performed to ascertain the potential of using inexpensive inorganic sorbents to control mercury emissions from coal-fired power plants without adverse impact on the salability fly ash, which is one of the major drawbacks of current control technologies based on activated carbon.

Radisav Vidic; Joseph Flora; Eric Borguet

2008-12-31T23:59:59.000Z

359

Passive vapor extraction feasibility study  

SciTech Connect (OSTI)

Demonstration of a passive vapor extraction remediation system is planned for sites in the 200 West Area used in the past for the disposal of waste liquids containing carbon tetrachloride. The passive vapor extraction units will consist of a 4-in.-diameter pipe, a check valve, a canister filled with granular activated carbon, and a wind turbine. The check valve will prevent inflow of air that otherwise would dilute the soil gas and make its subsequent extraction less efficient. The granular activated carbon is used to adsorb the carbon tetrachloride from the air. The wind turbine enhances extraction rates on windy days. Passive vapor extraction units will be designed and operated to meet all applicable or relevant and appropriate requirements. Based on a cost analysis, passive vapor extraction was found to be a cost-effective method for remediation of soils containing lower concentrations of volatile contaminants. Passive vapor extraction used on wells that average 10-stdft{sup 3}/min air flow rates was found to be more cost effective than active vapor extraction for concentrations below 500 parts per million by volume (ppm) of carbon tetrachloride. For wells that average 5-stdft{sup 3}/min air flow rates, passive vapor extraction is more cost effective below 100 ppm.

Rohay, V.J.

1994-06-30T23:59:59.000Z

360

Energy loss rate of a charged particle in HgTe/(HgTe, CdTe) quantum wells  

SciTech Connect (OSTI)

The energy loss rate (ELR) of a charged particle in a HgTe/(HgTe, CdTe) quantum well is investigated. We consider scattering of a charged particle by the bulk insulating states in this type of topological insulator. It is found that the ELR characteristics due to the intraband excitation have a linear energy dependence while those due to interband excitation depend on the energy exponentially. An interesting quantitative result is that for a large range of the incident energy, the mean inelastic scattering rate is around a few terahertz.

Chen, Qinjun; Sin Ang, Yee [School of Physics, University of Wollongong, New South Wales 2522 (Australia)] [School of Physics, University of Wollongong, New South Wales 2522 (Australia); Wang, Xiaolin [Institute for Superconducting and Electronic Materials, University of Wollongong, New South Wales 2522 (Australia)] [Institute for Superconducting and Electronic Materials, University of Wollongong, New South Wales 2522 (Australia); Lewis, R. A.; Zhang, Chao [School of Physics, University of Wollongong, New South Wales 2522 (Australia) [School of Physics, University of Wollongong, New South Wales 2522 (Australia); Institute for Superconducting and Electronic Materials, University of Wollongong, New South Wales 2522 (Australia)

2013-11-04T23:59:59.000Z

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


361

Enhancing Carbon Reactivity in Mercury Control in Lignite-Fired Systems  

SciTech Connect (OSTI)

This project was awarded through the U.S. Department of Energy (DOE) National Energy Technology Laboratory Program Solicitation DE-PS26-03NT41718-01. The Energy & Environmental Research Center (EERC) led a consortium-based effort to resolve mercury (Hg) control issues facing the lignite industry. The EERC team-the Electric Power Research Institute (EPRI); the URS Corporation; the Babcock & Wilcox Company; ADA-ES; Apogee; Basin Electric Power Cooperative; Otter Tail Power Company; Great River Energy; Texas Utilities; Montana-Dakota Utilities Co.; Minnkota Power Cooperative, Inc.; BNI Coal Ltd.; Dakota Westmoreland Corporation; the North American Coal Corporation; SaskPower; and the North Dakota Industrial Commission-demonstrated technologies that substantially enhanced the effectiveness of carbon sorbents to remove Hg from western fuel combustion gases and achieve a high level ({ge} 55% Hg removal) of cost-effective control. The results of this effort are applicable to virtually all utilities burning lignite and subbituminous coals in the United States and Canada. The enhancement processes were previously proven in pilot-scale and limited full-scale tests. Additional optimization testing continues on these enhancements. These four units included three lignite-fired units: Leland Olds Station Unit 1 (LOS1) and Stanton Station Unit 10 (SS10) near Stanton and Antelope Valley Station Unit 1 (AVS1) near Beulah and a subbituminous Powder River Basin (PRB)-fired unit: Stanton Station Unit 1 (SS1). This project was one of three conducted by the consortium under the DOE mercury program to systematically test Hg control technologies available for utilities burning lignite. The overall objective of the three projects was to field-test and verify options that may be applied cost-effectively by the lignite industry to reduce Hg emissions. The EERC, URS, and other team members tested sorbent injection technologies for plants equipped with electrostatic precipitators (ESPs) and spray dryer absorbers combined with fabric filters (SDAs-FFs). The work focused on technology commercialization by involving industry and emphasizing the communication of results to vendors and utilities throughout the project.

Chad Wocken; Michael Holmes; John Pavlish; Jeffrey Thompson; Katie Brandt; Brandon Pavlish; Dennis Laudal; Kevin Galbreath; Michelle Olderbak

2008-06-30T23:59:59.000Z

362

MERIT Hg System Design V.B. Graves  

E-Print Network [OSTI]

testing · The pump equipment operates in a range of 6000 Gauss to 300 Gauss (1 Tesla = 104 Gauss) Target system must deliver a stable, unconstrained jet of Hg into a 15 Tesla field #12;4 OAK RIDGE NATIONAL · Hydraulic pump (outside secondary containment) - Pump, motor, reservoir - Proportional, directional control

McDonald, Kirk

363

The new Hg-rich barium indium mercurides BaIn{sub x}Hg{sub 7?x} (x=3.1) and BaIn{sub x}Hg{sub 11?x} (x=02.8)  

SciTech Connect (OSTI)

The title compounds BaIn{sub x}Hg{sub 7?x} (x=3.1(1)) and BaIn{sub x}Hg{sub 11?x} (x=02.8) were synthesized from stoichiometric ratios of the elements in Ta crucibles. Their crystal structures have been determined using single crystal X-ray data. BaIn{sub x}Hg{sub 7?x} (x=3.1(1)) crystallizes in a new structure type (orthorhombic, oC16, space group Cmmm: a=512.02(1), b=1227.68(3), c=668.61(2) pm, Z=2, R1=0.0311). In the structure, the atoms of the three crystallographically different mixed In/Hg positions form planar nets of four-, six- and eight-membered rings. These nets are shifted against each other such that the four-membered rings form empty distorted cubes. The cubes are connected via common edges, corners and folded ladders, which are also found in BaIn{sub 2}/BaHg{sub 2} (KHg{sub 2} structure type) and BaIn (?-NaHg type). The Ba atoms are centered in the eight-membered rings and exhibit an overall coordination number of 20. The [BaM{sub 20}] polyhedra and twice as many distorted [M{sub 8}] cubes tesselate the space. BaIn{sub 2.8}Hg{sub 8.2} (cubic, cP36, space group Pm3{sup }m, a=961.83(1) pm, Z=3, R1=0.0243) is the border compound of the phase width BaIn{sub x}Hg{sub 11?x} of the rare BaHg{sub 11} structure type. In the structure, ideal [M{sub 8}] cubes (at the corners of the unit cell) and BaM{sub 20} polyhedra (at the edges of the unit cell) represent the building blocks comparable to the other new In mercuride. In accordance with the increased In/Hg content, additional M-pure regions appear: the center of the unit cell contains a huge [Hg(1)M(2){sub 12}M(3,4){sub 32}] polyhedron, a Hg-centered cuboctahedron of In/Hg atoms surrounded by a capped cantellated cube of 32 additional M atoms. For both structure types, the bonding situation and the coloring, i.e. the In/Hg distribution of the polyanionic network, are discussed considering the different sizes of the atoms and the charge distribution (Bader AIM charges), which have been calculated within the framework of FP-LAPW density functional theory. - Graphical abstract: BaIn{sub 2.6}Hg{sub 4.4}: distorted cubes [(In/Hg){sub 8}] (green, like in BaHg{sub 11}), folded ladders (violet, like in BaIn, BaHg{sub 2} and BaIn{sub 2}) and Ba coordination polyhedra [Ba(In/Hg){sub 20}] (blue, like in BaHg{sub 11}). - Highlights: The Hg-rich In-mercuride BaIn{sub 3.1}Hg{sub 3.9} crystallizes with a singular structure type. The phase width of the BaHg{sub 11} structure in BaIn{sub x}Hg{sub 11-x} ends at x=2.8. The relations of both compounds with other alkaline-earth mercurides are outlined. The Hg/In coloring of the polyanion is discussed considering the structure features. Bonding aspects are explored using band structure calculations.

Wendorff, Marco; Schwarz, Michael; Rhr, Caroline, E-mail: caroline@ruby.chemie.uni-freiburg.de

2013-07-15T23:59:59.000Z

364

Mitigation and Remediation of Mercury Contamination at the Y...  

Office of Environmental Management (EM)

and surface water Hg remediation strategy for adequacy in reducing Hg levels in the fish and to indentify opportunities to achieve cost and technical improvements andor to...

365

Increased Mercury Bioaccumulation Follows Water Quality Improvement  

SciTech Connect (OSTI)

Changes in physical and chemical characteristics of aquatic habitats made to reduce or eliminate ecological risks can sometimes have unforeseen consequences. Environmental management activities on the U.S. Dept. of Energy reservation in Oak Ridge, Tennessee,have succeeded in improving water quality in streams impacted by discharges fi-om industrial facilities and waste disposal sites. The diversity and abundance of pollution-sensitive components of the benthic macroinvertebrate communities of three streams improved after new waste treatment systems or remedial actions reduced inputs of various toxic chemicals. Two of the streams were known to be mercury-contaminated from historical spills and waste disposal practices. Waterborne mercury concentrations in the third were typical of uncontaminated systems. In each case, concentrations of mercury in fish, or the apparent biological availability of mercury increased over the period during which ecological metrics indicated improved water quality. In the system where waterborne mercury concentrations were at background levels, increased mercury bioaccumulation was probably a result of reduced aqueous selenium concentrations; however, the mechanisms for increased mercury accumulation in the other two streams remain under investigation. In each of the three systems, reduced inputs of metals and inorganic anions was followed by improvements in the health of aquatic invertebrate communities. However, this reduction in risk to aquatic invertebrates was accompanied by increased risk to humans and piscivorous wildlife related to increased mercury concentrations in fish.

Bogle, M.A.; Peterson, M.J.; Smith, J.G.; Southworth, G.R.

1999-09-15T23:59:59.000Z

366

Portable vapor diffusion coefficient meter  

DOE Patents [OSTI]

An apparatus for measuring the effective vapor diffusion coefficient of a test vapor diffusing through a sample of porous media contained within a test chamber. A chemical sensor measures the time-varying concentration of vapor that has diffused a known distance through the porous media. A data processor contained within the apparatus compares the measured sensor data with analytical predictions of the response curve based on the transient diffusion equation using Fick's Law, iterating on the choice of an effective vapor diffusion coefficient until the difference between the predicted and measured curves is minimized. Optionally, a purge fluid can forced through the porous media, permitting the apparatus to also measure a gas-phase permeability. The apparatus can be made lightweight, self-powered, and portable for use in the field.

Ho, Clifford K. (Albuquerque, NM)

2007-06-12T23:59:59.000Z

367

MERCURY HANDLING FOR THE TARGET SYSTEM FOR A MUON COLLIDER  

E-Print Network [OSTI]

MERCURY HANDLING FOR THE TARGET SYSTEM FOR A MUON COLLIDER Van Graves , ORNL, Oak Ridge, TN 37830 Factory is a free-stream mercury jet within a 20-T magnetic field being impacted by an 8-GeV proton beam. A pool of mercury serves as a receiving reservoir for the mercury and a dump for the unexpended proton

McDonald, Kirk

368

Thursday, March 15, 2007 POSTER SESSION II: MERCURY  

E-Print Network [OSTI]

Thursday, March 15, 2007 POSTER SESSION II: MERCURY 6:30 p.m. Fitness Center Dombard A. J. Hauck S. A. II Despinning Plus Global Contraction and the Orientation of Lobate Scarps on Mercury [#2026] We thermal models of Mercury. King S. D. A Possible Connection Between Convection in Mercury's Mantle

Rathbun, Julie A.

369

2003 Mercury Computer Systems, Inc. Optimizing System Compute  

E-Print Network [OSTI]

© 2003 Mercury Computer Systems, Inc. Optimizing System Compute Density for Deployed HPEC Electronics Engineering Mercury Computer Systems, Inc. rbanton@mc.com Richard Jaenicke, Director, Product Marketing Mercury Computer Systems, Inc. rjaenicke@mc.com #12;2 © 2002 Mercury Computer Systems, Inc.© 2003

Kepner, Jeremy

370

Laser Altimeter Observations from MESSENGER's First Mercury Flyby  

E-Print Network [OSTI]

REPORT Laser Altimeter Observations from MESSENGER's First Mercury Flyby Maria T. Zuber,1 * David E Barnouin-Jha,8 John K. Harmon10 A 3200-kilometers-long profile of Mercury by the Mercury Laser Altimeter compensated. Sampled craters on Mercury are shallower than their counterparts on the Moon, at least in part

Hauck II, Steven A.

371

Vapor deposition of hardened niobium  

DOE Patents [OSTI]

A method of coating ceramic nuclear fuel particles containing a major amount of an actinide ceramic in which the particles are placed in a fluidized bed maintained at ca. 800.degree. to ca. 900.degree. C., and niobium pentachloride vapor and carbon tetrachloride vapor are led into the bed, whereby niobium metal is deposited on the particles and carbon is deposited interstitially within the niobium. Coating apparatus used in the method is also disclosed.

Blocher, Jr., John M. (Columbus, OH); Veigel, Neil D. (Columbus, OH); Landrigan, Richard B. (Columbus, OH)

1983-04-19T23:59:59.000Z

372

Determination of certain trapping parameters in mercury sulphide (03B1-HgS) by Thermally Stimulated Conductivity  

E-Print Network [OSTI]

, 6, 7, 8] is 2.275 eV at liquid helium, 2.250 eV at liquid nitrogen and 2.100 eV at room temperature les résultats de nos mesures de courants stimulés thermiquement sur le sulfure de mercure. Celles profondeur du niveau (Et = 300 meV), la densité de pièges (Nt = 2,55 1012 cm- 3) et la section efficace de

Boyer, Edmond

373

Figure 2: The mercury jet target geometry. The proton beam and mercury jet cross at z=-37.5 cm.  

E-Print Network [OSTI]

Figure 2: The mercury jet target geometry. The proton beam and mercury jet cross at z=-37.5 cm. Figure 3: The layout of multiple proton beam entry directions relative to mercury jet at z=-75 cm. A PION of a free liquid mercury jet with an intense proton beam. We study the variation of meson production

McDonald, Kirk

374

THE LOCAL IMPACTS OF MERCURY EMISSIONS FROM COAL FIRED POWER PLANTS ON HUMAN HEALTH RISK. PROGRESS REPORT FOR THE PERIOD OF MARCH 2003 - MARCH 2003.  

SciTech Connect (OSTI)

This report presents a follow-up to previous assessments of the health risks of mercury that BNL performed for the Department of Energy. Methylmercury is an organic form of mercury that has been implicated as the form of mercury that impacts human health. A comprehensive risk assessment report was prepared (Lipfert et al., 1994) that led to several journal articles and conference presentations (Lipfert et al. 1994, 1995, 1996). In 2001, a risk assessment of mercury exposure from fish consumption was performed for 3 regions of the U.S (Northeast, Southeast, and Midwest) identified by the EPA as regions of higher impact from coal emissions (Sullivan, 2001). The risk assessment addressed the effects of in utero exposure to children through consumption of fish by their mothers. Two population groups (general population and subsistence fishers) were considered. Three mercury levels were considered in the analysis, current conditions based on measured data, and hypothetical reductions in Hg levels due to a 50% and 90% reduction in mercury emissions from coal fired power plants. The findings of the analysis suggested that a 90% reduction in coal-fired emissions would lead to a small reduction in risk to the general population (population risk reduction on the order of 10{sup -5}) and that the population risk is born by less than 1% of the population (i.e. high end fish consumers). The study conducted in 2001 focused on the health impacts arising from regional deposition patterns as determined by measured data and modeling. Health impacts were assessed on a regional scale accounting for potential percent reductions in mercury emissions from coal. However, quantitative assessment of local deposition near actual power plants has not been attempted. Generic assessments have been performed, but these are not representative of any single power plant. In this study, general background information on the mercury cycle, mercury emissions from coal plants, and risk assessment are provided to provide the basis for examining the impacts of local deposition. A section that covers modeling of local deposition of mercury emitted from coal power plants follows. The code ISCST3 was used with mercury emissions data from two power plants and local meteorological conditions to assess local deposition. The deposition modeling results were used to estimate the potential increase in mercury deposition that could occur in the vicinity of the plant. Increased deposition was assumed to lead to a linearly proportional increase in mercury concentrations in fish in local water bodies. Fish are the major pathway for human health impacts and the potential for increased mercury exposure was evaluated and the risks of such exposure estimated. Based on the findings recommendations for future work and conclusions are provided. Mercury is receiving substantial attention in a number of areas including: understanding of mercury deposition, bioaccumulation, and transport through the atmosphere, and improvements to the understanding of health impacts created by exposure to mercury. A literature review of key articles is presented as Appendix A.

SULLIVAN,T.M.LIPFERT,F.D.MORRIS,S.M.

2003-05-01T23:59:59.000Z

375

Treatment of mercury containing waste  

DOE Patents [OSTI]

A process is provided for the treatment of mercury containing waste in a single reaction vessel which includes a) stabilizing the waste with sulfur polymer cement under an inert atmosphere to form a resulting mixture and b) encapsulating the resulting mixture by heating the mixture to form a molten product and casting the molten product as a monolithic final waste form. Additional sulfur polymer cement can be added in the encapsulation step if needed, and a stabilizing additive can be added in the process to improve the leaching properties of the waste form.

Kalb, Paul D. (Wading River, NY); Melamed, Dan (Gaithersburg, MD); Patel, Bhavesh R (Elmhurst, NY); Fuhrmann, Mark (Babylon, NY)

2002-01-01T23:59:59.000Z

376

DFJ Mercury | Open Energy Information  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Office of InspectorConcentratingRenewable Solutions LLC JumpCrow Lake Wind JumpCuttings AnalysisDCDFJ Mercury Jump to:

377

Photoinduced Oxidation of Hg0 in the Waters from the St.  

E-Print Network [OSTI]

-A induced reactions. Doubling UV irradiation did not increase the reaction rate of Hg0 photooxidation food chain. Understanding the parameters that govern Hg0 oxidation is therefore crucial to assess

Morel, François M. M.

378

Field Testing of a Wet FGD Additive for Enhanced Mercury Control - Pilot-Scale Test Results  

SciTech Connect (OSTI)

This Topical Report summarizes progress on Cooperative Agreement DE-FC26-04NT42309, ''Field Testing of a Wet FGD Additive.'' The objective of the project is to demonstrate the use of a flue gas desulfurization (FGD) additive, Degussa Corporation's TMT-15, to prevent the reemissions of elemental mercury (Hg{sup 0}) in flue gas exiting wet FGD systems on coal-fired boilers. Furthermore, the project intends to demonstrate that the additive can be used to precipitate most of the mercury (Hg) removed in the wet FGD system as a fine TMT salt that can be separated from the FGD liquor and bulk solid byproducts for separate disposal. The project will conduct pilot and full-scale tests of the TMT-15 additive in wet FGD absorbers. The tests are intended to determine required additive dosage requirements to prevent Hg{sup 0} reemissions and to separate mercury from the normal FGD byproducts for three coal types: Texas lignite/Power River Basin (PRB) coal blend, high-sulfur Eastern bituminous coal, and low-sulfur Eastern bituminous coal. The project team consists of URS Group, Inc., EPRI, TXU Generation Company LP, Southern Company, and Degussa Corporation. TXU Generation has provided the Texas lignite/PRB co-fired test site for pilot FGD tests, Monticello Steam Electric Station Unit 3. Southern Company is providing the low-sulfur Eastern bituminous coal host site for wet scrubbing tests, as well as the pilot and full-scale jet bubbling reactor (JBR) FGD systems to be tested. A third utility, to be named later, will provide the high-sulfur Eastern bituminous coal full-scale FGD test site. Degussa Corporation is providing the TMT-15 additive and technical support to the test program. The project is being conducted in six tasks. Of the six project tasks, Task 1 involves project planning and Task 6 involves management and reporting. The other four tasks involve field testing on FGD systems, either at pilot or full scale. The four tasks include: Task 2 - Pilot Additive Testing in Texas Lignite Flue Gas; Task 3 - Full-scale FGD Additive Testing in High Sulfur Eastern Bituminous Flue Gas; Task 4 - Pilot Wet Scrubber Additive Tests at Yates; and Task 5 - Full-scale Additive Tests at Plant Yates. This topical report presents the results from the Task 2 and Task 4 pilot-scale additive tests. The Task 3 and Task 5 full-scale additive tests will be conducted later in calendar year 2006.

Gary M. Blythe

2006-03-01T23:59:59.000Z

379

Development of an electromagnetically actuated mercury microvalve  

SciTech Connect (OSTI)

The development of microscale fluid handling components has been recognized as a crucial element in the design of microscale chemical detection systems. Recently, work has been undertaken at Sandia National Laboratories to construct a valve that uses a small mercury droplet to control the flow of gas through capillary passages. Electromagnetic forces that are provided by small permanent magnets and a current supply are used to drive the mercury into position. Driving the mercury droplet into a tapered passage halts gas flow through a capillary, while surface tension forces prevent the mercury from passing through the passage. Models have been developed to describe the movement of the mercury droplet and the sealing of the gas passage, and millimeter-scale units have been tested to explore design options. Predictions from the model show that a valve with 10 micron sized features can seal against pressures up to 1.5 atmospheres. Experiments have highlighted the promise of mercury valves and demonstrated problems that can arise from contamination of the mercury.

Adkins, D.R.; Wong, C.C.

1998-08-01T23:59:59.000Z

380

The Vaporization Enthalpies and Vapor Pressures of Some Primary Amines of Pharmaceutical Importance by Correlation Gas  

E-Print Network [OSTI]

by Correlation Gas Chromatography Chase Gobble, Nigam Rath, and James Chickos* Department of Chemistry Information ABSTRACT: Vapor pressures, vaporization, and sublimation enthalpies of several pharmaceuticals and boiling temperatures when available. Sublimation enthalpies and vapor pressures are also evaluated for 1

Chickos, James S.

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


381

Fish mercury distribution in Massachusetts, USA lakes  

SciTech Connect (OSTI)

The sediment, water, and three species of fish from 24 of Massachusetts' (relatively) least-impacted water bodies were sampled to determine the patterns of variation in edible tissue mercury concentrations and the relationships of these patterns to characteristics of the water, sediment, and water bodies (lake, wetland, and watershed areas). Sampling was apportioned among three different ecological subregions and among lakes of differing trophic status. The authors sought to partition the variance to discover if these broadly defined concepts are suitable predictors of mercury levels in fish. Average muscle mercury concentrations were 0.15 mg/kg wet weight in the bottom-feeding brown bullheads (Ameriurus nebulosus); 0.31 mg/kg in the omnivorous yellow perch (Perca flavescens); and 0.39 mg/kg in the predaceous largemouth bass (Micropterus salmoides). Statistically significant differences in fish mercury concentrations between ecological subregions in Massachusetts, USA, existed only in yellow perch. The productivity level of the lakes (as deduced from Carlson's Trophic Status Index) was not a strong predictor of tissue mercury concentrations in any species. pH was a highly (inversely) correlated environmental variable with yellow perch and brown bullhead tissue mercury. Largemouth bass tissue mercury concentrations were most highly correlated with the weight of the fish (+), lake size (+), and source area sizes (+). Properties of individual lakes appear more important for determining fish tissue mercury concentrations than do small-scale ecoregional differences. Species that show major mercury variation with size or trophic level may not be good choices for use in evaluating the importance of environmental variables.

Rose, J.; Hutcheson, M.S.; West, C.R.; Pancorbo, O.; Hulme, K.; Cooperman, A.; DeCesare, G.; Isaac, R.; Screpetis, A.

1999-07-01T23:59:59.000Z

382

Evaluating Mercury Concentrations in Midwest Fish in Relationship to Mercury Emission Sources  

E-Print Network [OSTI]

International Energy Outlook estimates that world usage of coal will grow from 132 quadrillion British Thermal Units (BTU) in 2008 to over 202 quadrillion BTU in 2030 (USDOE, 2008). Even with improved mercury controls on power plants, this increase..., it is worthwhile to further examine the relationships between local sources of mercury and elevated concentrations of mercury in fish since these relationships may better inform control strategies, siting concerns, and overall energy policies. The author...

Robichaud, Jeffery

2008-12-19T23:59:59.000Z

383

Mercury Control for Plants Firing Texas Lignite and Equipped with ESP-wet FGD  

SciTech Connect (OSTI)

This report presents the results of a multi-year test program conducted as part of Cooperative Agreement DE-FC26-06NT42779, 'Mercury Control for Plants Firing Texas Lignite and Equipped with ESP-wet FGD.' The objective of this program was to determine the level of mercury removal achievable using sorbent injection for a plant firing Texas lignite fuel and equipped with an ESP and wet FGD. The project was primarily funded by the U.S. DOE National Energy Technology Laboratory. EPRI, NRG Texas, Luminant (formerly TXU), and AEP were project co-funders. URS Group was the prime contractor, and Apogee Scientific and ADA-ES were subcontractors. The host site for this program was NRG Texas Limestone Electric Generating Station (LMS) Units 1 and 2, located in Jewett, Texas. The plant fires a blend of Texas lignite and Powder River Basin (PRB) coal. Full-scale tests were conducted to evaluate the mercury removal performance of powdered sorbents injected into the flue gas upstream of the ESP (traditional configuration), upstream of the air preheater, and/or between electric fields within the ESP (Toxecon{trademark} II configuration). Phases I through III of the test program, conducted on Unit 1 in 2006-2007, consisted of three short-term parametric test phases followed by a 60-day continuous operation test. Selected mercury sorbents were injected to treat one quarter of the flue gas (e.g., approximately 225 MW equivalence) produced by Limestone Unit 1. Six sorbents and three injection configurations were evaluated and results were used to select the best combination of sorbent (Norit Americas DARCO Hg-LH at 2 lb/Macf) and injection location (upstream of the ESP) for a two-month performance evaluation. A mercury removal rate of 50-70% was targeted for the long-term test. During this continuous-injection test, mercury removal performance and variability were evaluated as the plant operated under normal conditions. Additional evaluations were made to determine any balance-of-plant impacts of the mercury control process, including those associated with ESP performance and fly ash reuse properties. Upon analysis of the project results, the project team identified several areas of interest for further study. Follow-on testing was conducted on Unit 2 in 2009 with the entire unit treated with injected sorbent so that mercury removal across the FGD could be measured and so that other low-ash impact technologies could be evaluated. Three approaches to minimizing ash impacts were tested: (1) injection of 'low ash impact' sorbents, (2) alterations to the injection configuration, and (3) injection of calcium bromide in conjunction with sorbent. These conditions were tested with the goal of identifying the conditions that result in the highest mercury removal while maintaining the sorbent injection at a rate that preserves the beneficial use of ash.

Katherine Dombrowski

2009-12-31T23:59:59.000Z

384

Vapor deposition of thin films  

DOE Patents [OSTI]

A highly pure thin metal film having a nanocrystalline structure and a process of preparing such highly pure thin metal films of, e.g., rhodium, iridium, molybdenum, tungsten, rhenium, platinum, or palladium by plasma assisted chemical vapor deposition of, e.g., rhodium(allyl).sub.3, iridium(allyl).sub.3, molybdenum(allyl).sub.4, tungsten(allyl).sub.4, rhenium(allyl).sub.4, platinum(allyl).sub.2, or palladium(allyl).sub.2 are disclosed. Additionally, a general process of reducing the carbon content of a metallic film prepared from one or more organometallic precursor compounds by plasma assisted chemical vapor deposition is disclosed.

Smith, David C. (Los Alamos, NM); Pattillo, Stevan G. (Los Alamos, NM); Laia, Jr., Joseph R. (Los Alamos, NM); Sattelberger, Alfred P. (Los Alamos, NM)

1992-01-01T23:59:59.000Z

385

VAPORIZATION THERMODYNAMICS OF KCl. COMBINING VAPOR PRESSURE AND GRAVIMETRIC DATA  

E-Print Network [OSTI]

.B. Department of Chemistry, Moscow State University, Moscow, 119899, Russia Bonnell D.W., Hastie J.W. National temperature chemistry situations, vapor pressures are typically less than 100 kPa. The molar volume is p = 101325 Pa). The subscript trs denotes that the changeisfor a transition, typically sublimation

Rudnyi, Evgenii B.

386

Future trends in environmental mercury concentrations: implications  

E-Print Network [OSTI]

Future trends in environmental mercury concentrations: implications for prevention strategies interactions among natural and human climate system components; objectively assess uncertainty in economic, monitor and verify greenhouse gas emissions and climatic impacts. This reprint is one of a series intended

387

Mercury sorbent delivery system for flue gas  

DOE Patents [OSTI]

The invention presents a device for the removal of elemental mercury from flue gas streams utilizing a layer of activated carbon particles contained within the filter fabric of a filter bag for use in a flue gas scrubbing system.

Klunder; ,Edgar B. (Bethel Park, PA)

2009-02-24T23:59:59.000Z

388

Symplectic Integrator Mercury: Bug Report  

E-Print Network [OSTI]

We report on a problem found in MERCURY, a hybrid symplectic integrator used for dynamical problems in Astronomy. The variable that keeps track of bodies' statuses is uninitialised, which can result in bodies disappearing from simulations in a non-physical manner. Some FORTRAN compilers implicitly initialise variables, preventing simulations from having this problem. With other compilers, simulations with a suitably large maximum number of bodies parameter value are also unaffected. Otherwise, the problem manifests at the first event after the integrator is started, whether from scratch or continuing a previously stopped simulation. Although the problem does not manifest in some conditions, explicitly initialising the variable solves the problem in a permanent and unconditional manner.

K. de Souza Torres; D. R. Anderson

2008-08-04T23:59:59.000Z

389

Detection of concealed mercury with thermal neutrons  

SciTech Connect (OSTI)

In the United States today, governments at all levels and the citizenry are paying increasing attention to the effects, both real and hypothetical, of industrial activity on the environment. Responsible modem industries, reflecting this heightened public and regulatory awareness, are either substituting benign materials for hazardous ones, or using hazardous materials only under carefully controlled conditions. In addition, present-day environmental consciousness dictates that we deal responsibly with legacy wastes. The decontamination and decommissioning (D&D) of facilities at which mercury was used or processed presents a variety of challenges. Elemental mercury is a liquid at room temperature and readily evaporates in air. In large mercury-laden buildings, droplets may evaporate from one area only to recondense in other cooler areas. The rate of evaporation is a function of humidity and temperature; consequently, different parts of a building may be sources or sinks of mercury at different times of the day or even the year. Additionally, although mercury oxidizes in air, the oxides decompose upon heating. Hence, oxides contained within pipes or equipment, may be decomposed when those pipes and equipment are cut with saws or torches. Furthermore, mercury seeps through the pores and cracks in concrete blocks and pads, and collects as puddles and blobs in void spaces within and under them.

Bell, Z.W.

1994-08-18T23:59:59.000Z

390

Hydrogen Cars and Water Vapor  

E-Print Network [OSTI]

misidentified as "zero-emissions vehicles." Fuel cell vehicles emit water vapor. A global fleet could have, with discernible effects on people and ecosystems. The broad environmental effects of fuel cell vehicles. This cycle is currently under way with hydrogen fuel cells. As fuel cell cars are suggested as a solution

Colorado at Boulder, University of

391

Vapor phase modifiers for oxidative coupling  

DOE Patents [OSTI]

Volatilized metal compounds retard vapor phase alkane conversion reactions in oxidative coupling processes that convert lower alkanes to higher hydrocarbons.

Warren, Barbara K. (Charleston, WV)

1991-01-01T23:59:59.000Z

392

Hg and Se capture and fly ash carbons from combustion of complex pulverized feed blends mainly of anthracitic coal rank in Spanish power plants  

SciTech Connect (OSTI)

In this work, the petrology and chemistry of fly ashes produced in a Spanish power plant from the combustion of complex pulverized feed blends made up of anthracitic/meta-anthracitic coals, petroleum, and natural coke are investigated. It was found that the behavior of fly ash carbons derived from anthracitic coals follows relatively similar patterns to those established for the carbons from the combustion of bituminous coals. Fly ashes were sampled in eight hoppers from two electrostatic precipitator (ESP) rows. The characterization of the raw ashes and their five sieved fractions (from {gt}150 to {lt}25 {mu}m) showed that glassy material, quartz, oxides, and spinels in different proportions are the main inorganic components. As for the organic fraction, the dominant fly ash carbons are anisotropic carbons, mainly unburned carbons derived from anthracitic vitrinite. The concentration of Se and Hg increased in ashes of the second ESP row, this increase being related to the higher proportion of anisotropic unburned carbons, particularly those largely derived from anthracitic vitrinite in the cooler ashes of the ESP (second row) and also related to the decrease in the flue gas temperature. This suggests that the flue gas temperature plays a major role in the concentration of mercury for similar ratios of unburned carbons. It was also found that Hg is highly concentrated in the medium-coarser fractions of the fly ashes ({gt} 45 {mu}m), there being a positive relationship between the amount of these carbons, which are apparently little modified during the combustion process, in the medium-coarse fractions of the ashes and the Hg retention. According to the results obtained, further research on this type of fly ash could be highly productive. 28 refs., 10 figs., 8 tabs.

I. Surez-Ruiz; J.C. Hower; G.A. Thomas [Instituto Nacional del Carbon (INCAR-CSIC), Oviedo (Spain)

2007-01-15T23:59:59.000Z

393

Elsevier Science 1 A Free Jet Hg Target Operating In a High Magnetic Field  

E-Print Network [OSTI]

University, Massachusetts Institute Of Technology, European Organization for Nuclear Research system and the mercury to CERN, decommissioning the experiment, and returning the mildly activated

McDonald, Kirk

394

VEE-0020- In the Matter of Mercury Fuel Service, Inc.  

Broader source: Energy.gov [DOE]

On April 9, 1996, Mercury Fuel Service, Inc. (Mercury) of Waterbury, Connecticut, filed an Application for Exception with the Office of Hearings and Appeals (OHA) of the Department of Energy (DOE)....

395

Seismic effects of the Caloris basin impact, Mercury  

E-Print Network [OSTI]

Striking geological features on Mercury's surface have been linked to tectonic disruption associated with the Caloris impact and have the potential to provide information on the interior structure of Mercury. The unusual ...

L, Jiangning

2011-01-01T23:59:59.000Z

396

Nested-grid simulation of mercury over North America  

E-Print Network [OSTI]

Chemistry and Physics Nested-grid simulation of mercury overY. Zhang et al. : Nested-grid simulation of mercury overand Chen, S. -Y. : Plume-in-grid modeling of atmospheric

2012-01-01T23:59:59.000Z

397

Removal of mercury from coal via a microbial pretreatment process  

SciTech Connect (OSTI)

A process for the removal of mercury from coal prior to combustion is disclosed. The process is based on use of microorganisms to oxidize iron, sulfur and other species binding mercury within the coal, followed by volatilization of mercury by the microorganisms. The microorganisms are from a class of iron and/or sulfur oxidizing bacteria. The process involves contacting coal with the bacteria in a batch or continuous manner. The mercury is first solubilized from the coal, followed by microbial reduction to elemental mercury, which is stripped off by sparging gas and captured by a mercury recovery unit, giving mercury-free coal. The mercury can be recovered in pure form from the sorbents via additional processing.

Borole, Abhijeet P. (Knoxville, TN); Hamilton, Choo Y. (Knoxville, TN)

2011-08-16T23:59:59.000Z

398

Evaluation of Sorbent Injection for Mercury Control  

SciTech Connect (OSTI)

The power industry in the U.S. is faced with meeting new regulations to reduce the emissions of mercury compounds from coal-fired plants. These regulations are directed at the existing fleet of nearly 1,100 boilers. These plants are relatively old with an average age of over 40 years. Although most of these units are capable of operating for many additional years, there is a desire to minimize large capital expenditures because of the reduced (and unknown) remaining life of the plant to amortize the project. Injecting a sorbent such as powdered activated carbon into the flue gas represents one of the simplest and most mature approaches to controlling mercury emissions from coal-fired boilers. This is the final site report for tests conducted at Laramie River Station Unit 3, one of five sites evaluated in this DOE/NETL program. The overall objective of the test program is to evaluate the capabilities of activated carbon injection at five plants: Sunflower Electric's Holcomb Station Unit 1, AmerenUE's Meramec Station Unit 2, Missouri Basin Power Project's Laramie River Station Unit 3, Detroit Edison's Monroe Power Plant Unit 4, and AEP's Conesville Station Unit 6. These plants have configurations that together represent 78% of the existing coal-fired generation plants. The goals for the program established by DOE/NETL are to reduce the uncontrolled mercury emissions by 50 to 70% at a cost 25 to 50% lower than the benchmark established by DOE of $60,000/lb mercury removed. The goals of the program were exceeded at Laramie River Station by achieving over 90% mercury removal at a sorbent cost of $3,980/lb ($660/oz) mercury removed for a coal mercury content of 7.9 lb/TBtu.

Sharon Sjostrom

2005-12-30T23:59:59.000Z

399

Partitioning of mercury, arsenic, selenium, boron, and chloride in a full-scale coal combustion process equipped with selective catalytic reduction, electrostatic precipitation, and flue gas desulfurization systems  

SciTech Connect (OSTI)

A full-scale field study was carried out at a 795 MWe coal-fired power plant equipped with selective catalytic reduction (SCR), an electrostatic precipitator (ESP), and wet flue gas desulfurization (FGD) systems to investigate the distribution of selected trace elements (i.e., mercury, arsenic, selenium, boron, and chloride) from coal, FGD reagent slurry, makeup water to flue gas, solid byproduct, and wastewater streams. Flue gases were collected from the SCR outlet, ESP inlet, FGD inlet, and stack. Concurrent with flue gas sampling, coal, bottom ash, economizer ash, and samples from the FGD process were also collected for elemental analysis. By combining plant operation parameters, the overall material balances of selected elements were established. The removal efficiencies of As, Se, Hg, and B by the ESP unit were 88, 56, 17, and 8%, respectively. Only about 2.5% of Cl was condensed and removed from flue gas by fly ash. The FGD process removed over 90% of Cl, 77% of B, 76% of Hg, 30% of Se, and 5% of As. About 90% and 99% of the FGD-removed Hg and Se were associated with gypsum. For B and Cl, over 99% were discharged from the coal combustion process with the wastewater. Mineral trona (trisodium hydrogendicarbonate dehydrate, Na{sub 3}H(CO{sub 3}){sub 2}.2H{sub 2}O) was injected before the ESP unit to control the emission of sulfur trioxide (SO{sub 3}). By comparing the trace elements compositions in the fly ash samples collected from the locations before and after the trona injection, the injection of trona did not show an observable effect on the partitioning behaviors of selenium and arsenic, but it significantly increased the adsorption of mercury onto fly ash. The stack emissions of mercury, boron, selenium, and chloride were for the most part in the gas phase. 47 refs., 3 figs., 11 tabs.

Chin-Min Cheng; Pauline Hack; Paul Chu; Yung-Nan Chang; Ting-Yu Lin; Chih-Sheng Ko; Po-Han Chiang; Cheng-Chun He; Yuan-Min Lai; Wei-Ping Pan [Western Kentucky University, Bowling Green, KY (United States). Institute for Combustion Science and Environmental Technology

2009-09-15T23:59:59.000Z

400

Vapor canister heater for evaporative emissions systems  

SciTech Connect (OSTI)

Automotive evaporative emissions systems use a charcoal canister to store evaporative hydrocarobn emissions. These stored vapors are later purged and burned during engine operation. Under certain conditions the engine cannot completely purge the canister of the stored fuel vapors, which results in a decreased vapor storage capacity in the canister. A self-regulating PTC (Positive Temperature Coefficient) heater has been developed to warm the purge air as it enters the canister, in order to provide thermal energy for increased release of the vapors from charcoal sites. This paper describes the construction and operation of the vapor canister heater as it relates to improved evaporative emission system performance.

Bishop, R.P.; Berg, P.G.

1987-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


401

Long-Term Carbon Injection Field Test for 90% Mercury Removal for a PRB Unit a Spray Dryer and Fabric Filter  

SciTech Connect (OSTI)

The power industry in the U.S. is faced with meeting regulations to reduce the emissions of mercury compounds from coal-fired plants. Injecting a sorbent such as powdered activated carbon (PAC) into the flue gas represents one of the simplest and most mature approaches to controlling mercury emissions from coal-fired boilers. The purpose of this test program was to evaluate the long-term mercury removal capability, long-term mercury emissions variability, and operating and maintenance (O&M) costs associated with sorbent injection on a configuration being considered for many new plants. Testing was conducted by ADA Environmental Solutions (ADA) at Rocky Mountain Powers (RMP) Hardin Station through funding provided by DOE/NETL, RMP, and other industry partners. The Hardin Station is a new plant rated at 121 MW gross that was first brought online in April of 2006. Hardin fires a Powder River Basin (PRB) coal and is configured with selective catalytic reduction (SCR) for NOx control, a spray dryer absorber (SDA) for SO2 control, and a fabric filter (FF) for particulate control. Based upon previous testing at PRB sites with SCRs, very little additional mercury oxidation from the SCR was expected at Hardin. In addition, based upon results from DOE/NETL Phase II Round I testing at Holcomb Station and results from similarly configured sites, low native mercury removal was expected across the SDA and FF. The main goal of this project was metsorbent injection was used to economically and effectively achieve 90% mercury control as measured from the air heater (AH) outlet to the stack for a period of ten months. This goal was achieved with DARCO Hg-LH, Calgon FLUEPAC-MC PLUS and ADA Power PAC PREMIUM brominated activated carbons at nominal loadings of 1.52.5 lb/MMacf. An economic analysis determined the twenty-year levelized cost to be 0.87 mills/kW-hr, or $15,000/lb Hg removed. No detrimental effects on other equipment or plant operations were observed. The results of this project also filled a data gap for plants firing PRB coal and configured with an SCR, SDA, and FF, as many new plants are being designed today. Another goal of the project was to evaluate, on a short-term basis, the mercury removal associated with coal additives and coal blending with western bituminous coal. The additive test showed that, at this site, the coal additive known as KNX was affective at increasing mercury removal while decreasing sorbent usage. Coal blending was conducted with two different western bituminous coals, and West Elk coal increased native capture from nominally 10% to 50%. Two additional co-benefits were discovered at this site. First, it was found that native capture increased from nominally 10% at full load to 50% at low load. The effect is believed to be due to an increase in mercury oxidation across the SCR caused by a corresponding decrease in ammonia injection when the plant reduces load. Less ammonia means more active oxidation sites in the SCR for the mercury. The second co-benefit was the finding that high ammonia concentrations can have a negative impact on mercury removal by powdered activated carbon. For a period of time, the plant operated with a high excess of ammonia injection necessitated by the plugging of one-third of the SCR. Under these conditions and at high load, the mercury control system could not maintain 90% removal even at the maximum feed rate of 3.5 lb/MMacf (pounds of mercury per million actual cubic feet). The plant was able to demonstrate that mercury removal was directly related to the ammonia injection rate in a series of tests where the ammonia rate was decreased, causing a corresponding increase in mercury removal. Also, after the SCR was refurbished and ammonia injection levels returned to normal, the mercury removal performance also returned to normal. Another goal of the project was to install a commercial-grade activated carbon injection (ACI) system and integrate it with new-generation continuous emissions monitors for mercury (Hg-CEMs) to allow automatic feedback control on outlet me

Sjostrom, Sharon; Amrhein, Jerry

2009-04-30T23:59:59.000Z

402

DOE Issues Final Mercury Storage Environmental Impact Statement: Texas Site Is Preferred for Long-Term Mercury Storage  

Broader source: Energy.gov [DOE]

WASHINGTON The Department of Energy has prepared a Final Long-Term Management and Storage of Elemental Mercury Environmental Impact Statement to analyze the potential environmental, human health, and socioeconomic impacts of elemental mercury storage at seven locations

403

Optical frequency standards based on mercury and aluminum ions  

E-Print Network [OSTI]

Optical frequency standards based on mercury and aluminum ions W. M. Itano, J. C. Bergquist, A-16 . Keywords: aluminum, atomic clocks, frequency standards, ion traps, mercury 1. INTRODUCTION Optical frequency standards based on the mercury ion and, more recently, the aluminum ion are under devel- opment

404

Mercury: Supporting Scalable Multi-Attribute Range Queries  

E-Print Network [OSTI]

Mercury: Supporting Scalable Multi-Attribute Range Queries Ashwin R. Bharambe Mukesh Agrawal 15213 Abstract This paper presents the design of Mercury, a scalable protocol for supporting multi-attribute range- based searches. Mercury differs from previous range-based query systems in that it supports mul

Keinan, Alon

405

Mercury/Waterfilling for Fixed Wireless OFDM Angel Lozano  

E-Print Network [OSTI]

Mercury/Waterfilling for Fixed Wireless OFDM Systems Angel Lozano Bell Labs (Lucent Technologies- mation is then given by the more general mercury/waterfilling policy. This paper illustrates the usance of mercury/waterfilling on frequency-selective OFDM channels with QAM constellations and it quantifies

Verdú, Sergio

406

MERCURY HANDLING FOR THE TARGET SYSTEM FOR A MUON COLLIDER  

E-Print Network [OSTI]

MERCURY HANDLING FOR THE TARGET SYSTEM FOR A MUON COLLIDER (IPAC12, WEPPD038) The target station a 15-20 T superconducting magnet. The target itself is a free mercury jet, moving at 20 m/s at an small angle to the magnetic axis, so as later to be collected in a mercury pool/beam dump. The replaceable

McDonald, Kirk

407

Powering Mercury's dynamo J.-P. Williams,1  

E-Print Network [OSTI]

Powering Mercury's dynamo J.-P. Williams,1 O. Aharonson,1 and F. Nimmo2 Received 6 July 2007 magnetic field of Mercury has implications for the interior structure of the planet and its thermal (2007), Powering Mercury's dynamo, Geophys. Res. Lett., 34, L21201, doi:10.1029/ 2007GL031164. 1

Nimmo, Francis

408

2003 Mercury Computer Systems, Inc. Session 5: Current &  

E-Print Network [OSTI]

© 2003 Mercury Computer Systems, Inc. Session 5: Current & Emerging Standards Session 5: Current & Emerging Standards Craig Lund, Chief Technology Officer Mercury Computer Systems, Inc. High Performance Embedded Computing (HPEC) Conference September 2003 #12;© 2003 Mercury Computer Systems, Inc. Agenda

Kepner, Jeremy

409

Wednesday, March 25, 2009 SPECIAL SESSION: MESSENGER AT MERCURY  

E-Print Network [OSTI]

Wednesday, March 25, 2009 SPECIAL SESSION: MESSENGER AT MERCURY: A GLOBAL PERSPECTIVE. T. MESSENGER's Newly Global Perspective on Mercury: Some Implications for Interior Evolution [#1750] MESSENGER's first two flybys of Mercury have revealed a planet with a richer history of magmatism

Rathbun, Julie A.

410

Exploring Mercury: Scientific Results from the MESSENGER Mission  

E-Print Network [OSTI]

#12;Exploring Mercury: Scientific Results from the MESSENGER Mission Larry R. Nittler Carnegie-Cahill · MESSENGER Science Team, Engineers, Mission Operations (APL) #12;Mars Mercury · Naked-eye planet, but very difficult to observe due to proximity to Sun May 12, 2011, from NZ (M. White, Flickr) Mercury Venus Jupiter

Rhoads, James

411

2003 Mercury Computer Systems, Inc. Beamforming for Radar  

E-Print Network [OSTI]

© 2003 Mercury Computer Systems, Inc. Beamforming for Radar Systems on COTS Heterogeneous ComputingHeterogeneous Computing PlatformsPlatforms Jeffrey A. Rudin Mercury Computer Systems, Inc. High Performance Embedded Computing (HPEC) Conference September 23, 2003 #12;2© 2003 Mercury Computer Systems, Inc. Outline

Kepner, Jeremy

412

MERCURY IN THE ATMOSPHERE, BIOSPHERE, AND POLICY SPHERE  

E-Print Network [OSTI]

MERCURY IN THE ATMOSPHERE, BIOSPHERE, AND POLICY SPHERE: Insights from a global 3D land.S. National Science Foundation Atmospheric Chemistry Program #12;FROM ATMOSPHERE TO FISH: MERCURY RISING Ice core from Wyoming [Schuster et al., ES&T 2002] Mercury deposition has increased by 300% since

Selin, Noelle Eckley

413

Mercury Beam Dump Simulations Tristan Davenne Ottone Caretta  

E-Print Network [OSTI]

Mercury Beam Dump Simulations Tristan Davenne Ottone Caretta STFC Rutherford Appleton Laboratory, UK 2nd Princeton-Oxford High Power Target Meeting 6-7 November-2008 #12;Mercury beam dump design from NUFACT Feasibility Study #12;Peter Loveridge, November-2008 Mercury beam dump design from NUFACT

McDonald, Kirk

414

Mercury's thermo-chemical evolution from numerical models constrained  

E-Print Network [OSTI]

Mercury's thermo-chemical evolution from numerical models constrained by MESSENGER observations Globe de Paris, France #12;Basics facts about Mercury · Semi-major axis: 0.39 AU · 3:2 spin Earth!) · Black body temperature: 440 K #12;Exploration of Mercury Mariner10 ·First spacecraft to use

Cerveny, Vlastislav

415

Mercury exosphere I. Global circulation model of its sodium component  

E-Print Network [OSTI]

Mercury exosphere I. Global circulation model of its sodium component Francois Leblanc a,*, R 2010 Accepted 27 April 2010 Available online 5 May 2010 Keywords: Mercury, Atmosphere Aeronomy a b s t r a c t Our understanding of Mercury's sodium exosphere has improved considerably in the last 5

Johnson, Robert E.

416

Mercury warning given to north state anglers By Ryan Sabalow  

E-Print Network [OSTI]

Mercury warning given to north state anglers By Ryan Sabalow Monday, June 7, 2010 A new study the highest levels of mercury contamination in the state. Although anglers arent being warned to wean,905 fish in 272 of Californias popular lakes and reservoirs for mercury, PCBs, DDT and other contaminants

417

Mercury reuses several external software tools developed by ORNL  

E-Print Network [OSTI]

Mercury reuses several external software tools developed by ORNL DAAC and other organizations-on,canopychemistryaccpclimatecollectionseoslandvalidationFIFEFIFEfollow-on fluxnethydroclimatologycollectionsmodelarchivenetprimaryproductivityNPPNBIIMAST- DCUSANPNIABINDataONEWENDI Mercury's architecture includes 1) a harvesting engine was packaged in such a way that all the Mercury projects will use the same harvester scripts, but each project

418

Mercury and Freon: Temperature Emulation and Management for Server Systems  

E-Print Network [OSTI]

Mercury and Freon: Temperature Emulation and Management for Server Systems Taliver Heath Dept by simulators and real measurements. In this paper, we introduce Mercury, a soft- ware suite that avoids data. Most importantly, Mercury runs the entire software stack natively, enables repeatable experiments

Bianchini, Ricardo

419

Thursday, March 26, 2009 POSTER SESSION II: MERCURY  

E-Print Network [OSTI]

Thursday, March 26, 2009 POSTER SESSION II: MERCURY 6:30 p.m. Town Center Exhibit Area Gómez-Perez N. Wicht J. Magnetic Field at Mercury: Effects of External Sources on Planetary Dynamos [#1634] In Mercury, magnetospheric currents induce a magnetic field at the top of the core. We study dynamo

Rathbun, Julie A.

420

Mercury: Supporting Scalable Multi-Attribute Range Ashwin R. Bharambe  

E-Print Network [OSTI]

Mercury: Supporting Scalable Multi-Attribute Range Queries Ashwin R. Bharambe ashu Carnegie Mellon University Pittsburgh, PA 15213 ABSTRACT This paper presents the design of Mercury, a scalable pro- tocol for supporting multi-attribute range-based searches. Mercury differs from previous

Krishnamurthy, Arvind

Note: This page contains sample records for the topic "mercury vapor hg" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.