Powered by Deep Web Technologies
Note: This page contains sample records for the topic "mercury hg sulfur" 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.


1

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

2

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

3

Mercury (Hg) and methyl mercury (MMHg) bioaccumulation in three fish species (sea food) from Persian Gulf  

Science Journals Connector (OSTI)

In this study, mercury (Hg) and methyl mercury (MMHg) were determined in three fish species including benthic, benthopelagic and pelagic fish from Arvand river, northwest of Persian Gulf. Mercury and methyl mercu...

Sajad Abdolvand; Sahar Kayedinejad Esfahani…

2014-09-01T23:59:59.000Z

4

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

5

Safety Bulletin 2005-08: Safe Management of Mercury (Hg)  

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

SAFETY & HEALTH SAFETY & HEALTH SAFETY & HEALTH BULLETIN Assistant Secretary for Environment, Safety & Health * U.S. Department of Energy * Washington, DC 20585 Safe Management of Mercury (Hg) DOE/EH-0697 Issue No. 2005-08 June 2005 PURPOSE This Bulletin provides information on a safety concern that may impact operations at Department of Energy (DOE) facilities. Specifically, the concern is the safe handling of mercury and mercury compounds. BACKGROUND Mercury is found in small amounts in thermometers, manometers, and barometers and in larger quantities at DOE facilities - ranging from amounts found in scientific equipment to tons in remediation waste at burial sites and hundreds of tons at the DOE stockpile storage facility in Oak Ridge.

6

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

7

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

8

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

9

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.

10

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

11

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

12

Enhanced Elemental Mercury Removal from Coal-fired Flue Gas by Sulfur-chlorine Compounds  

SciTech Connect (OSTI)

Oxidation of Hg0 with any oxidant or converting it to a particle-bound form can facilitate its removal. Two sulfur-chlorine compounds, sulfur dichloride (SCl2) and sulfur monochloride (S2Cl2), were investigated as oxidants for Hg0 by gas phase reaction and by surface-involved reactions in the presence of flyash or activated carbon. The gas phase reaction rate constants between Hg0 and the sulfur/chlorine compounds were determined, and the effects of temperature and the main components in flue gases were studied. The gas phase reaction between Hg0 and SCl2 is shown to be more rapid than the gas phase reaction with chlorine, and the second order rate constant was 9.1(+-0.5) x 10-18 mL-molecules-1cdots-1 at 373oK. Nitric oxide (NO) inhibited the gas phase reaction of Hg0 with sulfur-chlorine compounds. The presence of flyash or powdered activated carbon in flue gas can substantially accelerate the reaction. The predicted Hg0 removal is about 90percent with 5 ppm SCl2 or S2Cl2 and 40 g/m3 of flyash in flue gas. The combination of activated carbon and sulfur-chlorine compounds is an effective alternative. We estimate that co-injection of 3-5 ppm of SCl2 (or S2Cl2) with 2-3 Lb/MMacf of untreated Darco-KB is comparable in efficiency to the injection of 2-3 Lb/MMacf Darco-Hg-LH. Extrapolation of kinetic results also indicates that 90percent of Hg0 can be removed if 3 Lb/MMacf of Darco-KB pretreated with 3percent of SCl2 or S2Cl2 is used. Unlike gas phase reactions, NO exhibited little effect on Hg0 reactions with SCl2 or S2Cl2 on flyash or activated carbon. Mercuric sulfide was identified as one of the principal products of the Hg0/SCl2 or Hg0/S2Cl2 reactions. Additionally, about 8percent of SCl2 or S2Cl2 in aqueous solutions is converted to sulfide ions, which would precipitate mercuric ion from FGD solution.

Chang, Shih-Ger; Yan, Nai-Qiang; Qu, Zan; Chi, Yao; Qiao, Shao-Hua; Dod, Ray; Chang, Shih-Ger; Miller, Charles

2008-07-02T23:59:59.000Z

13

Sorbent Injection for Small ESP Mercury Control in Low Sulfur Eastern Bituminous Coal Flue Gas  

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

Sorbent InjectIon for Small eSP Sorbent InjectIon for Small eSP mercury control In low Sulfur eaStern bItumInouS coal flue GaS Background Full-scale field testing has demonstrated the effectiveness of activated carbon injection (ACI) as a mercury-specific control technology for certain coal-fired power plants, depending on the plant's coal feedstock and existing air pollution control device configuration. In a typical configuration, powdered activated carbon (PAC) is injected downstream of the plant's air heater and upstream of the existing particulate control device - either an electrostatic precipitator (ESP) or a fabric filter (FF). The PAC adsorbs the mercury from the combustion flue gas and is subsequently captured along with the fly ash in the ESP or FF. ACI can have some negative side

14

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

15

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

16

Coal Cleaning Using Resonance Disintegration for Mercury and Sulfur Reduction Prior to Combustion  

SciTech Connect (OSTI)

Coal-cleaning processes have been utilized to increase the heating value of coal by extracting ash-forming minerals in the coal. These processes involve the crushing or grinding of raw coal followed by physical separation processes, taking advantage of the density difference between carbonaceous particles and mineral particles. In addition to the desired increase in the heating value of coal, a significant reduction of the sulfur content of the coal fed to a combustion unit is effected by the removal of pyrite and other sulfides found in the mineral matter. WRI is assisting PulseWave to develop an alternate, more efficient method of liberating and separating the undesirable mineral matter from the carbonaceous matter in coal. The approach is based on PulseWave's patented resonance disintegration technology that reduces that particle size of materials by application of destructive resonance, shock waves, and vortex generating forces. Illinois No.5 coal, a Wyodak coal, and a Pittsburgh No.8 coal were processed using the resonance disintegration apparatus then subjected to conventional density separations. Initial microscopic results indicate that up to 90% of the pyrite could be liberated from the coal in the machine, but limitations in the density separations reduced overall effectiveness of contaminant removal. Approximately 30-80% of the pyritic sulfur and 30-50% of the mercury was removed from the coal. The three coals (both with and without the pyritic phase separated out) were tested in WRI's 250,000 Btu/hr Combustion Test Facility, designed to replicate a coal-fired utility boiler. The flue gases were characterized for elemental, particle bound, and total mercury in addition to sulfur. The results indicated that pre-combustion cleaning could reduce a large fraction of the mercury emissions.

Andrew Lucero

2005-04-01T23:59:59.000Z

17

Impact of additives for enhanced sulfur dioxide removal on re-emissions of mercury in wet flue gas desulfurization  

Science Journals Connector (OSTI)

Abstract The wet flue gas desulfurization process (FGD) in fossil fired power plants offers the advantage of simultaneously removing SO2 and other water soluble pollutants, such as certain oxidized mercury compounds (Hg2+). In order to maximize SO2 removal efficiency of installed FGD units, organic additives can be utilized. In the context of multi-pollutant control by wet FGD, the effect of formic and adipic acid on redox reactions of dissolved mercury compounds is investigated with a continuously operated lab-scale test-rig. For sulfite ( SO 3 2 - ) concentrations above a certain critical value, their potential as reducing agent leads to rapidly increasing formation and re-emission of elemental mercury (Hg0). Increasing chloride concentration and decreasing pH and slurry temperature have been identified as key factors for depressing Hg0 re-emissions. Both organic additives have a negative impact on Hg-retention and cause increased Hg0 re-emissions in the wet FGD process, with formic acid being the significantly stronger reducing agent. Different pathways of Hg2+ reduction were identified by qualitative interpretation of the pH-dependence and by comparison of activation enthalpies and activation entropies. While the first mechanism proposed identifies SO 3 2 - as reducing agent and is therefore relevant for any FGD process, the second mechanism involves the formate anion, thus being exclusively relevant for \\{FGDs\\} utilizing formic acid as additive.

Barna Heidel; Melanie Hilber; Günter Scheffknecht

2014-01-01T23:59:59.000Z

18

A case study of mercury and methylmercury dynamics in a Hg-contaminated municipal wastewater treatment plant  

Science Journals Connector (OSTI)

A study of total Hg (Hg) and methylmercury (MeHg) was performed in a 40 mgd capacity municipal sewage treatment plant in which elemental Hg was used as ... the Hg seals with mechanical seals. A mass balance condu...

C. C. Gilmour; N. S. Bloom

1995-02-01T23:59:59.000Z

19

A Case Study of Mercury and Methylmercury Dynamics in a Hg-Contaminated Municipal Wastewater Treatment Plant  

Science Journals Connector (OSTI)

A study of total Hg (Hg) and methylmercury (MeHg) was performed in a 40 mgd capacity municipal sewage treatment plant in which elemental Hg was used as ... the Hg seals with mechanical seals. A mass balance condu...

C. C. Gilmour; N. S. Bloom

1995-01-01T23:59:59.000Z

20

Reduction of Hg(II) to Hg(0) by Magnetite. | EMSL  

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

of Hg(II) to Hg(0) by Magnetite. Reduction of Hg(II) to Hg(0) by Magnetite. Abstract: Mercury (Hg) is a highly toxic element, and its contamination of groundwater presents a...

Note: This page contains sample records for the topic "mercury hg sulfur" 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

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

22

Enhanced Elemental Mercury Removal from Coal-fired Flue Gas by Sulfur-chlorine Compounds  

E-Print Network [OSTI]

III T; Murphy J T. DOE/NETL’s Phase II Mercury ControlFired Power Plants, DOE/NETL Mercury R&D Program Review,

Miller, Nai-Qiang Yan-Zan Qu Yao Chi Shao-Hua Qiao Ray Dod Shih-Ger Chang Charles

2008-01-01T23:59:59.000Z

23

Probing Mercury's Partnering Preferences  

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

Preferences Probing Mercury's Partnering Preferences Merc.gif Why it Matters: Mercury (Hg) is a major global pollutant arising from both natural and anthropogenic sources....

24

Near-Zero Emissions Oxy-Combustion Flue Gas Purification Task 2: SOx/Nox/Hg Removal for High Sulfur Coal  

SciTech Connect (OSTI)

The goal of this project is to develop a near-zero emissions flue gas purification technology for existing PC (pulverized coal) power plants that are retrofitted with oxy-combustion technology. The objective of Task 2 of this project was to evaluate an alternative method of SOx, NOx and Hg removal from flue gas produced by burning high sulfur coal in oxy-combustion power plants. The goal of the program was not only to investigate a new method of flue gas purification but also to produce useful acid byproduct streams as an alternative to using a traditional FGD and SCR for flue gas processing. During the project two main constraints were identified that limit the ability of the process to achieve project goals. 1) Due to boiler island corrosion issues >60% of the sulfur must be removed in the boiler island with the use of an FGD. 2) A suitable method could not be found to remove NOx from the concentrated sulfuric acid product, which limits sale-ability of the acid, as well as the NOx removal efficiency of the process. Given the complexity and safety issues inherent in the cycle it is concluded that the acid product would not be directly saleable and, in this case, other flue gas purification schemes are better suited for SOx/NOx/Hg control when burning high sulfur coal, e.g. this project's Task 3 process or a traditional FGD and SCR.

Nick Degenstein; Minish Shah; Doughlas Louie

2012-05-01T23:59:59.000Z

25

Mercury (Hg) mineral evolution: A mineralogical record of supercontinent assembly, changing ocean geochemistry, and the emerging terrestrial biosphere  

Science Journals Connector (OSTI)

...Almaden district (primary mineralization 427-380 Ma) led to at least one additional pulse of hydrothermal Hg...chlor-alkali industry; and a new generation of compact fluorescent light bulbs. Burning of Hg-enriched coal and petroleum adds...

Robert M. Hazen; Joshua Golden; Robert T. Downs; Grethe Hystad; Edward S. Grew; David Azzolini; Dimitri A. Sverjensky

26

SULFUR POLYMER STABILIZATION/SOLIDIFICATION TREATABILITY STUDY OF MERCURY CONTAMINATED SOIL FROM THE Y-12 SITE  

E-Print Network [OSTI]

has cleanup responsibilities on the DOE Oak Ridge Reservation and is investigating potential mercury to support the remediation of the Y-12 site. URS CH2M Oak Ridge LLC (UCOR) under its prime contract with DOE THE Y-12 SITE P. D. Kalb, L. Milian, and S. P. Yim Informal Report Prepared for URS CH2M OAK RIDGE LLC

Johnson, Peter D.

27

Mercury oxidation promoted by a selective catalytic reduction catalyst under simulated Powder River Basin coal combustion conditions  

SciTech Connect (OSTI)

A bench-scale reactor consisting of a natural gas burner and an electrically heated reactor housing a selective catalytic reduction (SCR) catalyst was constructed for studying elemental mercury (Hg{sup 0}) oxidation under SCR conditions. A low sulfur Powder River Basin (PRB) subbituminous coal combustion fly ash was injected into the entrained-flow reactor along with sulfur dioxide (SO{sub 2}), nitrogen oxides (NOx), hydrogen chloride (HCl), and trace Hg{sup 0}. Concentrations of Hg{sup 0} and total mercury (Hg) upstream and downstream of the SCR catalyst were measured using a Hg monitor. The effects of HCl concentration, SCR operating temperature, catalyst space velocity, and feed rate of PRB fly ash on Hg0 oxidation were evaluated. It was observed that HCl provides the source of chlorine for Hg{sup 0} oxidation under simulated PRB coal-fired SCR conditions. The decrease in Hg mass balance closure across the catalyst with decreasing HCl concentration suggests that transient Hg capture on the SCR catalyst occurred during the short test exposure periods and that the outlet speciation observed may not be representative of steady-state operation at longer exposure times. Increasing the space velocity and operating temperature of the SCR led to less Hg{sup 0} oxidized. Introduction of PRB coal fly ash resulted in slightly decreased outlet oxidized mercury (Hg{sup 2+}) as a percentage of total inlet Hg and correspondingly resulted in an incremental increase in Hg capture. The injection of ammonia (NH{sub 3}) for NOx reduction by SCR was found to have a strong effect to decrease Hg oxidation. The observations suggest that Hg{sup 0} oxidation may occur near the exit region of commercial SCR reactors. Passage of flue gas through SCR systems without NH{sub 3} injection, such as during the low-ozone season, may also impact Hg speciation and capture in the flue gas. 18 refs., 7 figs., 3 tabs.

Chun W. Lee; Shannon D. Serre; Yongxin Zhao; Sung Jun Lee; Thomas W. Hastings [U.S. Environmental Protection Agency, Research Triangle Park, NC (United States). Office of Research and Development, National Risk Management Research Laboratory

2008-04-15T23:59:59.000Z

28

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

29

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

30

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

31

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

32

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

33

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

34

NETL: Mercury Emissions Control Technologies - Testing of Mercury Control  

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

Testing of Mercury Control with Calcium-Based Sorbents and Oxidizing Agents Testing of Mercury Control with Calcium-Based Sorbents and Oxidizing Agents Southern Research Institute, Birmingham, Alabama Subcontractor- ARCADIS Geraghty & Miller The overall goal of this project is to test the effectiveness of calcium-based sorbents and oxidizing agents for controlling mercury emissions from coal-fired power plant boilers. ARCADIS Geraghty & Miller, with EPA support, has developed calcium-based sorbents to remove SO2 and mercury simultaneously. The sorbents consist of hydrated lime (Ca(OH)2) and an added oxidant and a silica-modified calcium (CaSiO3) with an added oxidant. The mercury capacity in ug Hg/g sorbent for the two sorbents is 20 and 110-150, respectively, verses a mercury capacity for the current standard sorbent, activated carbon, of 70-100. The advantages of a lime based sorbent verses carbon is lower cost, simultaneous removal of sulfur, and allowance of ash to be utilized for a cement additive.

35

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

36

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

37

Discovery of HgCu-bearing metal-sulfide assemblages in a primitive H-3 chondrite: Towards a new insight in early solar system processes  

E-Print Network [OSTI]

Mercury (Hg) is the most volatile non-gaseous element. The Hg solar abundance (Lodders, 2003; Lodders et

Ma, Chi

38

Near-Zero Emissions Oxy-Combustion Flue Gas Purification Task 3: SOx/NOx/Hg Removal for Low Sulfur Coal  

SciTech Connect (OSTI)

The goal of this project was to develop a near-zero emissions flue gas purification technology for existing PC (pulverized coal) power plants that are retrofitted with oxycombustion technology. The objective of Task 3 of this project was to evaluate an alternative method of SOx, NOx and Hg removal from flue gas produced by burning low sulfur coal in oxy-combustion power plants. The goal of the program was to conduct an experimental investigation and to develop a novel process for simultaneously removal of SOx and NOx from power plants that would operate on low sulfur coal without the need for wet-FGD & SCRs. A novel purification process operating at high pressures and ambient temperatures was developed. Activated carbonâ??s catalytic and adsorbent capabilities are used to oxidize the sulfur and nitrous oxides to SO{sub 3} and NO{sub 2} species, which are adsorbed on the activated carbon and removed from the gas phase. Activated carbon is regenerated by water wash followed by drying. The development effort commenced with the screening of commercially available activated carbon materials for their capability to remove SO{sub 2}. A bench-unit operating in batch mode was constructed to conduct an experimental investigation of simultaneous SOx and NOx removal from a simulated oxyfuel flue gas mixture. Optimal operating conditions and the capacity of the activated carbon to remove the contaminants were identified. The process was able to achieve simultaneous SOx and NOx removal in a single step. The removal efficiencies were >99.9% for SOx and >98% for NOx. In the longevity tests performed on a batch unit, the retention capacity could be maintained at high level over 20 cycles. This process was able to effectively remove up to 4000 ppm SOx from the simulated feeds corresponding to oxyfuel flue gas from high sulfur coal plants. A dual bed continuous unit with five times the capacity of the batch unit was constructed to test continuous operation and longevity. Full-automation was implemented to enable continuous operation (24/7) with minimum operator supervision. Continuous run was carried out for 40 days. Very high SOx (>99.9%) and NOx (98%) removal efficiencies were also achieved in a continuous unit. However, the retention capacity of carbon beds for SOx and NOx was decreased from ~20 hours to ~10 hours over a 40 day period of operation, which was in contrast to the results obtained in a batch unit. These contradictory results indicate the need for optimization of adsorption-regeneration cycle to maintain long term activity of activated carbon material at a higher level and thus minimize the capital cost of the system. In summary, the activated carbon process exceeded performance targets for SOx and NOx removal efficiencies and it was found to be suitable for power plants burning both low and high sulfur coals. More efforts are needed to optimize the system performance.

Monica Zanfir; Rahul Solunke; Minish Shah

2012-06-01T23:59:59.000Z

39

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

40

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

Note: This page contains sample records for the topic "mercury hg sulfur" 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

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

42

DOE Mercury Control Research  

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

Mercury Control Research Mercury Control Research Air Quality III: Mercury, Trace Elements, and Particulate Matter September 9-12, 2002 Rita A. Bajura, Director National Energy Technology Laboratory www.netl.doe.gov 169330 RAB 09/09/02 2 Potential Mercury Regulations MACT Standards * Likely high levels of Hg reduction * Compliance: 2007 Clean Power Act of 2001 * 4-contaminant control * 90% Hg reduction by 2007 Clear Skies Act of 2002 * 3-contaminant control * 46% Hg reduction by 2010 * 70% Hg reduction by 2018 * Hg emission trading President Bush Announcing Clear Skies Initiative February 14, 2002 169330 RAB 09/09/02 3 Uncertainties Mercury Control Technologies * Balance-of-plant impacts * By-product use and disposal * Capture effectiveness with low-rank coals * Confidence of performance 169330 RAB 09/09/02 4

43

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...

44

Analysis of Strategies for Reducing Multiple Emissions from Electric Power Plants: Sulfur Dioxide, Nitrogen Oxides, Carbon Dioxide, and Mercury and a Renewable Portfolio Standard  

Gasoline and Diesel Fuel Update (EIA)

3 3 ERRATA Analysis of Strategies for Reducing Multiple Emissions from Electric Power Plants: Sulfur Dioxide, Nitrogen Oxides, Carbon Dioxide, and Mercury and a Renewable Portfolio Standard July 2001 Energy Information Administration Office of Integrated Analysis and Forecasting U.S. Department of Energy Washington, DC 20585 This Service Report was prepared by the Energy Information Administration, the independent statistical and analytical agency within the Department of Energy. The information contained herein should be attributed to the Contacts This report was prepared by the Office of Integrated Analysis and Forecasting, Energy Information Adminis- tration. General questions concerning the report may be directed to Mary J. Hutzler (202/586-2222, mhutzler @eia.doe.gov), Director of the Office of Integrated Analysis and Forecasting, Scott B. Sitzer (202/586-2308,

45

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

46

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

47

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.

48

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

49

PILOT-SCALE EVALUATION OF THE IMPACT OF SELECTIVE CATALYTIC REDUCTION FOR NOx ON MERCURY SPECIATION  

SciTech Connect (OSTI)

Full-scale tests in Europe and bench-scale tests in the United States have indicated that the catalyst, normally vanadium/titanium metal oxide, used in the selective catalytic reduction (SCR) of NO{sub x}, may promote the formation of Hg{sup 2+} and/or particulate-bound mercury (Hg{sub p}). To investigate the impact of SCR on mercury speciation, pilot-scale screening tests were conducted at the Energy & Environmental Research Center. The primary research goal was to determine whether the catalyst or the injection of ammonia in a representative SCR system promotes the conversion of Hg{sup 0} to Hg{sup 2+} and/or Hg{sub p} and, if so, which coal types and parameters (e.g., rank and chemical composition) affect the degree of conversion. Four different coals, three eastern bituminous coals and a Powder River Basin (PRB) subbituminous coal, were tested. Three tests were conducted for each coal: (1) baseline, (2) NH{sub 3} injection, and (3) SCR of NO{sub x}. Speciated mercury, ammonia slip, SO{sub 3}, and chloride measurements were made to determine the effect the SCR reactor had on mercury speciation. It appears that the impact of SCR of NO{sub x} on mercury speciation is coal-dependent. Although there were several confounding factors such as temperature and ammonia concentrations in the flue gas, two of the eastern bituminous coals showed substantial increases in Hg{sub p} at the inlet to the ESP after passing through an SCR reactor. The PRB coal showed little if any change due to the presence of the SCR. Apparently, the effects of the SCR reactor are related to the chloride, sulfur and, possibly, the calcium content of the coal. It is clear that additional work needs to be done at the full-scale level.

Dennis L. Laudal; John H. Pavlish; Kevin C. Galbreath; Jeffrey S. Thompson; Gregory F. Weber; Everett Sondreal

2000-12-01T23:59:59.000Z

50

Mercury speciation in the Persian Gulf sediments  

Science Journals Connector (OSTI)

The concentrations of total mercury (Hg) and methyl mercury (MMHg) were determined in 78 marine sediments in the Iranian coastal waters of the Persian Gulf along nine transects perpendicular to the coastline....?...

Homira Agah; Marc Elskens…

2009-10-01T23:59:59.000Z

51

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

52

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

53

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

54

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

55

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

56

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

57

Microsoft Word - HgAcBr  

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

August 2013 August 2013 Quantification of the Mercury Adsorption Mechanism on Brominated Activated Carbon The primary anthropogenic source of mercury (Hg) emissions into the atmosphere is coal- fired power utilities. This work explores materials designed for Hg capture to be applied in the ductwork of a power plant to prevent Hg release into the atmosphere. Bench-scale com- bustion experiments have been carried out, in which sorbent materials were placed in a simulated flue gas stream doped with ppb levels of Hg. The sorbent surfaces were probed using x-ray absorption spectroscopy to determine the mechanism of Hg binding and to ultimately improve solvent design. The spectroscopy data was analyzed alongside results from density functional theory (DFT) for benchmarking so that DFT can be used as a

58

Isotope Effect of Mercury Diffusion in Air  

Science Journals Connector (OSTI)

Isotope fractionation describes the separation of a reservoir with one isotope composition into “fractions” with different isotope compositions due to small isotopic differences in equilibrium partitioning, rates of mass transfer, or rates of transformation. ... (29) ?202Hg is the value most frequently used to examine mass dependent fractionation of mercury isotopes as 202Hg is the heaviest mercury isotope without significant isobaric interferences. ...

Paul G. Koster van Groos; Bradley K. Esser; Ross W. Williams; James R. Hunt

2013-12-23T23:59:59.000Z

59

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

60

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

Note: This page contains sample records for the topic "mercury hg sulfur" 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

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

62

Dissolved gaseous mercury behavior in shallow water estuaries  

E-Print Network [OSTI]

The formation of dissolved gaseous mercury (DGM) can be an important pathway for mercury removal from an aquatic environment. DGM evasional fluxes from an aquatic system can account for up to 95% of atmospheric Hg and its deposition pathways. While...

Landin, Charles Melchor

2009-05-15T23:59:59.000Z

63

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.

64

Dissolved Organic Matter Kinetically Controls Mercury Bioavailability to Bacteria  

Science Journals Connector (OSTI)

Predicting the bioavailability of inorganic mercury (Hg) to bacteria that produce the potent bioaccumulative neurotoxin monomethylmercury remains one of the greatest challenges in predicting the environmental fate and transport of Hg. Dissolved organic ...

Sophie A. Chiasson-Gould; Jules M. Blais; Alexandre J. Poulain

2014-02-13T23:59:59.000Z

65

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 no immediate effect on mercury removal. In 0.8 M HNO3 with the addition of K2Cr2O7, the reaction is first at 25 °C. For mercury absorption in Hg(II) obtained by HgCl2 injection, the presence of HNO3 greatly

Rochelle, Gary T.

66

Investigation of the relationship between particulate-bound mercury and properties of fly ash in a full-scale 100 MWe pulverized coal combustion boiler  

SciTech Connect (OSTI)

The properties of fly ash in coal-fired boilers influence the emission of mercury from power plants into the environment. In this study, seven different bituminous coals were burned in a full-scale 100 MWe pulverized coal combustion boiler and the derived fly ash samples were collected from a mechanical hopper (MH) and an electrostatic precipitator hopper (ESP). The mercury content, specific surface area (SSA), unburned carbon, and elemental composition of the fly ash samples were analyzed to evaluate the correlation between the concentration of particulate-bound mercury and the properties of coal and fly ash. For a given coal, it was found that the mercury content in the fly ash collected from the ESP was greater than in the fly ash samples collected from the MHP. This phenomenon may be due to a lower temperature of flue gas at the ESP (about 135{sup o}C) compared to the temperature at the air preheater (about 350{sup o}C). Also, a significantly lower SSA observed in MH ash might also contribute to the observation. A comparison of the fly ash samples generated from seven different coals using statistical methods indicates that the mercury adsorbed on ESP fly ashes has a highly positive correlation with the unburned carbon content, manganese content, and SSA of the fly ash. Sulfur content in coal showed a significant negative correlation with the Hg adsorption. Manganese in fly ash is believed to participate in oxidizing volatile elemental mercury (Hg{sup 0}) to ionic mercury (Hg{sup 2+}). The oxidized mercury in flue gas can form a complex with the fly ash and then get removed before the flue gas leaves the stack of the boiler.

Sen Li; Chin-Min Cheng; Bobby Chen; Yan Cao; Jacob Vervynckt; Amanda Adebambo; Wei-Ping Pan [Western Kentucky University, Bowling Green, KY (United States). Institute for Combustion Science and Environmental Technology

2007-12-15T23:59:59.000Z

67

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

68

Predictable SCR co-benefits for mercury control  

SciTech Connect (OSTI)

A test program, performed in cooperation with Dominion Power and the Babcock and Wilcox Co., was executed at Dominion Power's Mount Storm power plant in Grant County, W. Va. The program was focused on both the selective catalytic reduction (SCR) catalyst capability to oxide mercury as well as the scrubber's capability to capture and retain the oxidized mercury. This article focuses on the SCR catalyst performance aspects. The Mount Storm site consists of three units totaling approximately 1,660 MW. All units are equipped with SCR systems for NOx control. A full-scale test to evaluate the effect of the SCR was performed on Unit 2, a 550 MWT-fired boiler firing a medium sulfur bituminous coal. This test program demonstrated that the presence of an SCR catalyst can significantly affect the mercury speciation profile. Observation showed that in the absence of an SCR catalyst, the extent of oxidation of element a mercury at the inlet of the flue gas desulfurization system was about 64%. The presence of a Cornertech SCR catalyst improved this oxidation to levels greater than 95% almost all of which was captured by the downstream wet FGD system. Cornertech's proprietary SCR Hg oxidation model was used to accurately predict the field results. 1 ref., 2 figs., 1 tab.

Pritchard, S. [Cormtech Inc. (USA)

2009-01-15T23:59:59.000Z

69

It's Elemental - The Element Mercury  

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

Gold Gold Previous Element (Gold) The Periodic Table of Elements Next Element (Thallium) Thallium The Element Mercury [Click for Isotope Data] 80 Hg Mercury 200.59 Atomic Number: 80 Atomic Weight: 200.59 Melting Point: 234.32 K (-38.83°C or -37.89°F) Boiling Point: 629.88 K (356.73°C or 674.11°F) Density: 13.5336 grams per cubic centimeter Phase at Room Temperature: Liquid Element Classification: Metal Period Number: 6 Group Number: 12 Group Name: none What's in a name? Named after the planet Mercury. Mercury's chemical symbol comes from the Greek word hydrargyrum, which means "liquid silver." Say what? Mercury is pronounced as MER-kyoo-ree. History and Uses: Mercury was known to the ancient Chinese and Hindus and has been found in 3500 year old Egyptian tombs. Mercury is not usually found free in nature

70

A vareity of Hg capture solutions are available  

SciTech Connect (OSTI)

While vacating the Clean Air Mercury Rule (CAMR) has postponed implementation of capturing mercury emitted by coal-fired power plants improvements in ways to capture and monitor mercury have continued. One method of enhancing Hg capture from FGD and SCR is to treat the coal by adding a halogen, such as calcium bromide in Alstom's KNX process prior to combustion. Power plants without FGD usually use sorbent injection, mostly an activated carbon, upstream of a particulate control device. 1 fig.

Blankinship, S.

2009-06-15T23:59:59.000Z

71

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

72

DOE-NETLs Mercury R&D Program  

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

DOE's DOE's Phase II Mercury Control Technology Field Testing Program American Coal Council's 2005 Mercury & Multi- Emissions Conference March 22-24, 2005 St. Louis, MO Thomas J. Feeley, III thomas.feeley@netl.doe.gov National Energy Technology Laboratory MEC2_Ottawa_May 25 2005 Power Plant Mercury Control Baghouse or ESP FGD Boiler Stack Cleaning SCR Hg 75 ton/yr Hg in coal Current Emissions 48 ton/yr out stack Hg Hg Hg Hg 27 ton/yr Sorbent Injection Oxidizing Systems Hg Specific Control Co-Benefit Control ACS Monthly Meeting November 4 2004 DOE Mercury Control RD&D Portfolio Polishing Technology * MerCAP(tm) Sorbent Injection * Activated carbon * Amended silicates * Halogenated AC * Ca-based sorbents * Chemically treated sorbents * COHPAC/Toxecon(tm) * Thief sorbents Boiler * Combustion modification

73

Pilot-scale study of the effect of selective catalytic reduction catalyst on mercury speciation in Illinois and Powder River Basin coal combustion flue gases  

SciTech Connect (OSTI)

A study was conducted to investigate the effect of selective catalytic reduction (SCR) catalyst on mercury (Hg) speciation in bituminous and subbituminous coal combustion flue gases. Three different Illinois Basin bituminous coals (from high to low sulfur (S) and chlorine (Cl)) and one Powder River Basin (PRB) subbituminous coal with very low S and very low Cl were tested in a pilot-scale combustor equipped with an SCR reactor for controlling nitrogen oxides (NO{sub x}) emissions. The SCR catalyst induced high oxidation of elemental Hg (Hg{sup 0}), decreasing the percentage of Hg{sup 0} at the outlet of the SCR to values <12% for the three Illinois coal tests. The PRB coal test indicated a low oxidation of Hg{sup 0} by the SCR catalyst, with the percentage of Hg{sup 0} decreasing from {approximately} 96% at the inlet of the reactor to {approximately} 80% at the outlet. The low Cl content of the PRB coal and corresponding low level of available flue gas Cl species were believed to be responsible for low SCR Hg oxidation for this coal type. The test results indicated a strong effect of coal type on the extent of Hg oxidation. 16 refs., 4 figs., 3 tabs.

Lee, C.W.; Srivastava, R.K.; Ghorishi, S.B.; Karwowski, J.; Hastings, T.H.; Hirschi, J.C. [US Environmental Protection Agency, Triangle Park, NC (United States)

2006-05-15T23:59:59.000Z

74

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

75

Study on PCB 101, PCB 153, mercury and methyl mercury content in blue crab Portunus Pelagicus from Khuzestan shore (Persian Gulf)  

Science Journals Connector (OSTI)

Distribution of polychlorinated biphenyl (PCB 101, PCB 153), Mercury (Hg) and methyl mercury (MMHg) in muscle, gill and hepatopancreas of blue swimming crab Portunus segnis from Persian Gulf were investigated. In...

Abdolah Raeisi Sarasiab; Mehdi Hosseini

2014-06-01T23:59:59.000Z

76

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

77

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

78

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

79

Thief carbon catalyst for oxidation of mercury in effluent stream  

DOE Patents [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

80

Sediment transport and Hg recovery in Lavaca Bay, as evaluated from radionuclide and Hg distributions  

SciTech Connect (OSTI)

Mercury was released in the late 1960s from a chloralkali facility managed by ALCOA and deposited into sediments of Lavaca Bay, TX. Sediments have recorded this event as a well-defined subsurface concentration maximum. Radionuclide, mercury, X-radiography, and grain size data from sediment cores taken in 1997 at 15 stations in Lavaca bay were used to assess sediment and Hg movements in the bay. Sediment accumulation rates were calculated from bomb fallout nuclide ({sup 137}Cs, {sup 239,240}Pu) peaks in 1963 and from the steady-state delivery of {sup 210}Pb from the atmosphere. Sedimentation rates are highest at near-shore sites near the ALCOA facility and generally decrease away from shore. Sedimentation rates in some areas are likely influenced by anthropogenic activities such as dredging. Particle reworking, as assessed from {sup 7}Be measurements, is generally restricted to the upper 2--7 cm of sediments. Numerical simulations of Hg profiles using measured sedimentation and mixing parameters indicate that at most sites high remnant mercury concentrations at 15--60 cm depth cannot supply substantial amounts of Hg to surface sediments. Assuming no future Hg supplies, Hg concentrations in surface sediments are predicted to decrease exponentially with a recovery half-time of 4 {+-} 2 years.

Santschi, P.H.; Allison, M.A.; Asbill, S.; Perlet, A.B. [Texas A and M Univ., Galveston, TX (United States)] [Texas A and M Univ., Galveston, TX (United States); Cappellino, S. [Parametrix, Inc., Houston, TX (United States)] [Parametrix, Inc., Houston, TX (United States); Dobbs, C.; McShea, L. [Aluminum Co. of America, Point Comfort, TX (United States)] [Aluminum Co. of America, Point Comfort, TX (United States)

1999-02-01T23:59:59.000Z

Note: This page contains sample records for the topic "mercury hg sulfur" 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 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

82

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

83

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

84

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

85

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

86

Method development for the simultaneous determination of methylmercury and inorganic mercury in seafood  

Science Journals Connector (OSTI)

Abstract This paper reports the method development for the simultaneous determination of methylmercury (MeHg+) and inorganic mercury (iHg) species in seafood samples. The study focused on the extraction and quantification of MeHg+ (the most toxic species) by liquid chromatography coupled to on-line UV irradiation and cold vapour atomic fluorescence spectroscopy (LC-UV-CV-AFS), using \\{HCl\\} 4 mol L?1 as the extractant agent. Accuracy of the method has been verified by analysing three certified reference materials and different spiked samples. The values found for total Hg and MeHg+ for the \\{CRMs\\} did not differ significantly from certified values at a 95% confidence level, and recoveries between 85% and 97% for MeHg+, based on spikes, were achieved. The detection limits (LODs) obtained were 0.001 mg Hg kg?1 for total mercury, 0.0003 mg Hg kg?1 for MeHg+ and 0.0004 mg Hg kg?1 for iHg. The quantification limits (LOQs) established were 0.003 mg Hg kg?1 for total mercury, 0.0010 mg Hg kg?1 for MeHg+ and 0.0012 mg Hg kg?1 for iHg. Precision for each mercury species was established, being ? 12% in terms of RSD in all cases. Finally, the developed method was applied to 24 seafood samples from different origins and total mercury contents. The concentrations for Total Hg, MeHg+ and iHg ranged from 0.07 to 2.33, 0.003–2.23 and 0.006–0.085 mg Hg kg?1, respectively. The established analytical method allows to obtain results for mercury speciation in less than 1 one hour including both, sample pretreatment and measuring step.

Ariane V. Zmozinski; Sergio Carneado; Carmen Ibáñez-Palomino; Àngels Sahuquillo; José Fermín López-Sánchez; Márcia M. da Silva

2014-01-01T23:59:59.000Z

87

Effect of Chemical Speciation on Toxicity of Mercury to Escherichia coli Biofilms and Planktonic Cells  

Science Journals Connector (OSTI)

Effect of Chemical Speciation on Toxicity of Mercury to Escherichia coli Biofilms and Planktonic Cells ... charged forms of mercuric chloride (HgCl3-/HgCl42-) induced less light prodn. ...

Isaac Najera; Chu-Ching Lin; Golenaz Adeli Kohbodi; Jennifer A. Jay

2005-03-25T23:59:59.000Z

88

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

89

Songbirds as sentinels of mercury in terrestrial habitats of eastern North America  

Science Journals Connector (OSTI)

Mercury (Hg) is a globally distributed environmental contaminant with a variety of deleterious effects in fish, wildlife, and humans. Breeding songbirds may be useful sentinels for Hg across diverse habitats b...

Allyson K. Jackson; David C. Evers; Evan M. Adams; Daniel A. Cristol…

2014-12-01T23:59:59.000Z

90

Trimeric perfluoro-ortho-phenylene mercury as a building block for supramolecular materials  

E-Print Network [OSTI]

-coordinated to the mercury center through Hg-Carene bonds ranging from 2.3 to 2.7 ?. Weaker interactions are observed between aromatic substrates and the mercury center of neutral organomercurial derivatives. With Hg-Carene distances in the range of 3...-coordinated to the mercury center through Hg-Carene bonds ranging from 2.3 to 2.7 ?. Weaker interactions are observed between aromatic substrates and the mercury center of neutral organomercurial derivatives. With Hg-Carene distances in the range of 3...

Haneline, Mason Reames

2006-04-12T23:59:59.000Z

91

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.

92

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

93

Microsoft Word - Vapor Phase Elemental Sulfur Tech Brief DRAFT bbl 08-24.docx  

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

AT A GLANCE AT A GLANCE  eliminates excavation expense  applicable to large or small sites  straightforward deployment  uses heat to distribute sulfur throughout a soil  mercury reacts with sulfur to form immobile and insoluble minerals  patent applied for TechBrief Vapor Phase Elemental Sulfur Amendment for Sequestering Mercury in Contaminated Soil Scientists at the Savannah River National Laboratory (SRNL) have identified a method of targeting mercury in contaminated soil zone by use of sulfur vapor heated gas. Background Mercury contamination in soil is a common problem in the environment. The most common treatment is excavation - a method that works well for small sites where the

94

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

95

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

96

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

97

Modeling mercury in power plant plumes  

SciTech Connect (OSTI)

Measurements of speciated mercury (Hg) downwind of coal-fired power plants suggest that the Hg{sup II}/(Hg{sup 0} + Hg{sup II}) ratio decreases significantly between the point of emission and the downwind ground-level measurement site, but that the SO{sub 2}/(Hg{sup 0} + Hg{sup II}) ratio is conserved. The authors simulated nine power plant plume events with the Reactive & Optics Model of Emissions (ROME), a reactive plume model that includes a comprehensive treatment of plume dispersion, transformation, and deposition. The model simulations fail to reproduce such a depletion in Hg{sup II}. A sensitivity study of the impact of the Hg{sup II} dry deposition velocity shows that a difference in dry deposition alone cannot explain the disparity. Similarly, a sensitivity study of the impact of cloud chemistry on results shows that the effect of clouds on Hg chemistry has only minimal impact. Possible explanations include Hg{sup II} reduction to Hg{sup 0} in the plume, rapid reduction of Hg{sup II} to Hg{sup 0} on ground surfaces, and/or an overestimation of the Hg{sup II} fraction in the power plant emissions. The authors propose that a chemical reaction not included in current models of atmospheric mercury reduces Hg{sup II} to Hg{sup 0} in coal-fired power plant plumes. The incorporation of two possible reduction pathways for Hg{sup II} shows better agreement between the model simulations and the ambient measurements. These potential Hg{sup II} to Hg{sup 0} reactions need to be studied in the laboratory to investigate this hypothesis. Because the speciation of Hg has a significant effect on Hg deposition, models of the fate and transport of atmospheric Hg may need to be modified to account for the reduction of Hg{sup II} in coal-fired power plant plumes if such a reaction is confirmed in further experimental investigations. 31 refs., 2 figs., 6 tabs.

Kristen Lohman; Christian Seigneur; Eric Edgerton; John Jansen [Atmospheric & Environmental Research, Inc., San Ramon, CA (United States)

2006-06-15T23:59:59.000Z

98

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

99

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

100

Mercury pollution in Doha (Qatar) coastal environment  

SciTech Connect (OSTI)

Surface water and sediment samples were collected from the Doha coastal area and analyzed for content of physico-chemical forms of mercury. Dissolved reactive Hg represented 81.0% of the total dissolved Hg. Organic Hg contributed only 5.0% of total Hg. Mercury showed a strong tendency to be associated with suspended matter in Doha coastal waters, as it represented about 73.0% of the total. Total Hg in bulk Doha surface sediments fluctuated between 0.14 and 1.75 [mu]g g[sup [minus]1] dry weight, with an average of 0.54 [+-] 0.46 [mu]g g[sup [minus]1] dry weight. The sediment fraction past 63 [mu]m contained 0.73 [+-] 0.60 [mu]g g[sup [minus]1] dry weight total Hg. Leachable and methyl Hg averaged 0.10 [+-] 0.11 and 0.02 [+-] 0.03 [mu]g g[sup [minus]1] dry weight, respectively, in the < 63-[mu]m sediment fraction. There is a general trend for all Hg species determined in water and sediments to decrease seaward. The significantly elevated Hg levels at certain locations indicated that the main Hg sources to Doha coastal environment are leachate from the solid waste disposal site, the two harbors, and surface-water discharge.

Al-Madfa, H.; Dahab, O.A.; Holail, H. (Univ. of Qatar, Doha (Qatar). Dept. of Geology)

1994-05-01T23:59:59.000Z

Note: This page contains sample records for the topic "mercury hg sulfur" 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

Evaluating the Role of Mercury Chemistry Community Multiscale Air Quality Model  

E-Print Network [OSTI]

Chemical Species Results 54 Ozone 54 Nitrogen Dioxide 55 Sulfur Dioxide 56 A.2 Mercury Wet Deposition 59 A, and with ambient observations for ozone (O3), nitrogen dioxide (NO2), and sulfur dioxide (SO2) at two sites

Wisconsin at Madison, University of

102

NETL: Mercury Emissions Control Technologies - Bench Scale Kinetics of  

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

Bench Scale Kinetics of Mercury Reactions in FGD Liquors Bench Scale Kinetics of Mercury Reactions in FGD Liquors When research into the measurement and control of Hg emissions from coal-fired power plants began in earnest in the early 1990s, it was observed that oxidized mercury can be scrubbed at high efficiency in wet FGD systems, while elemental mercury can not. In many cases, elemental mercury concentrations were observed to increase slightly across wet FGD systems, but this was typically regarded as within the variability of the measurement methods. However, later measurements have shown substantial re-emissions from some FGD systems. The goal of this project is to develop a fundamental understanding of the aqueous chemistry of mercury (Hg) absorbed by wet flue gas desulfurization (FGD) scrubbing liquors. Specifically, the project will determine the chemical reactions that oxidized mercury undergoes once absorbed, the byproducts of those reactions, and reaction kinetics.

103

SULFUR POLYMER ENCAPSULATION.  

SciTech Connect (OSTI)

Sulfur polymer cement (SPC) is a thermoplastic polymer consisting of 95 wt% elemental sulfur and 5 wt% organic modifiers to enhance long-term durability. SPC was originally developed by the U.S. Bureau of Mines as an alternative to hydraulic cement for construction applications. Previous attempts to use elemental sulfur as a construction material in the chemical industry failed due to premature degradation. These failures were caused by the internal stresses that result from changes in crystalline structure upon cooling of the material. By reacting elemental sulfur with organic polymers, the Bureau of Mines developed a product that successfully suppresses the solid phase transition and significantly improves the stability of the product. SPC, originally named modified sulfur cement, is produced from readily available, inexpensive waste sulfur derived from desulfurization of both flue gases and petroleum. The commercial production of SPC is licensed in the United States by Martin Resources (Odessa, Texas) and is marketed under the trade name Chement 2000. It is sold in granular form and is relatively inexpensive ({approx}$0.10 to 0.12/lb). Application of SPC for the treatment of radioactive, hazardous, and mixed wastes was initially developed and patented by Brookhaven National Laboratory (BNL) in the mid-1980s (Kalb and Colombo, 1985; Colombo et al., 1997). The process was subsequently investigated by the Commission of the European Communities (Van Dalen and Rijpkema, 1989), Idaho National Engineering Laboratory (Darnell, 1991), and Oak Ridge National Laboratory (Mattus and Mattus, 1994). SPC has been used primarily in microencapsulation applications but can also be used for macroencapsulation of waste. SPC microencapsulation has been demonstrated to be an effective treatment for a wide variety of wastes, including incinerator hearth and fly ash; aqueous concentrates such as sulfates, borates, and chlorides; blowdown solutions; soils; and sludges. It is not recommended for treatment of wastes containing high concentrations of nitrates because of potentially dangerous reactions between sulfur, nitrate, and trace quantities of organics. Recently, the process has been adapted for the treatment of liquid elemental mercury and mercury contaminated soil and debris.

KALB, P.

2001-08-22T23:59:59.000Z

104

A Cavity Ring-Down Spectroscopy Mercury Continuous Emission Monitor  

SciTech Connect (OSTI)

The Sensor Research & Development Corporation (SRD) has undertaken the development of a Continuous Emissions Monitor (CEM) for mercury based on the technique of Cavity Ring-Down Spectroscopy (CRD). The project involved building an instrument for the detection of trace levels of mercury in the flue gas emissions from coal-fired power plants. The project has occurred over two phases. The first phase concentrated on the development of the ringdown cavity and the actual detection of mercury. The second phase dealt with the construction and integration of the sampling system, used to carry the sample from the flue stack to the CRD cavity, into the overall CRD instrument. The project incorporated a Pulsed Alexandrite Laser (PAL) system from Light Age Incorporated as the source to produce the desired narrow band 254 nm ultra-violet (UV) radiation. This laser system was seeded with a diode laser to bring the linewidth of the output beam from about 150 GHz to less than 60 MHz for the fundamental beam. Through a variety of non-linear optics the 761 nm fundamental beam is converted into the 254 nm beam needed for mercury detection. Detection of the mercury transition was verified by the identification of the characteristic natural isotopic structure observed at lower cavity pressures. The five characteristic peaks, due to both natural isotopic abundance and hyperfine splitting, provided a unique identifier for mercury. SRD scientists were able to detect mercury in air down below 10 parts-per-trillion by volume (pptr). This value is dependent on the pressure and temperature within the CRD cavity at the time of detection. Sulfur dioxide (SO{sub 2}) absorbs UV radiation in the same spectral region as mercury, which is a significant problem for most mercury detection equipment. However, SRD has not only been able to determine accurate mercury concentrations in the presence of SO{sub 2}, but the CRD instrument can in fact determine the SO{sub 2} concentration as well. Detection of mercury down to the low hundreds of pptr has been accomplished in the presence of SO{sub 2} at concentration levels much higher than that found in typical flue gas emissions. SRD scientists extended the interferent testing to each individual component found in flue gas. It was found that only SO{sub 2} had a significant effect on the ring-down decay curve. Upon completion of testing the components of flue gas individually a simulated flue gas stream was used to test to the CRD instrument. The result showed accurate detection of mercury down to levels below 100 pptr in a simulated flue gas stream with the concentrations of the various components above that found in a typical untreated flue gas. A sampling system was designed and integrated into the CRD instrument to carry the sample from the flue gas stack to the CRD cavity. The sampling system was constructed so that it could be placed very close to the sampling port. SRD scientists were able to couple the UV laser light into an optical fiber, which is then sent to the sampling system. This allows the laser system to be isolated from the sampling system. Initial long-term testing revealed a couple of problems related to the stability of the output frequency of the laser system. These problems have been successfully dealt with by incorporating specific software solutions into the overall data acquisition program. The project culminated in a field test conducted at the DOE/NETL pilot plant facility in Pittsburgh, Pennsylvania. The object of the test was the evaluation of a cavity ringdown spectrometer constructed for the detection of TOTAL vapor phase mercury as a continuous emission monitor (CEM). Although there is the potential for the instrument to determine the amount of speciation between neutral elemental mercury (Hg{sup (o)}) and oxidized mercury (Hg{sup (+2)}), the initial test plan was to concentrate on the measurement of the total mercury. Another added benefit is that the measurements will report the sulfur dioxide (SO 2) concentration throughout the test. This report concludes the technical work asso

Christopher C. Carter

2004-12-15T23:59:59.000Z

105

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

106

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

107

Mercury contamination in a 54-m core from lake Huleh  

Science Journals Connector (OSTI)

... for Hg by optical emission spectroscopy4'5. These results were confirmed by another laboratory using flameless atomic absorption spectroscopy. Mercury concentrations in the Huleh mud ranged from 2.36 to ...

U. M. COWGILL

1975-08-07T23:59:59.000Z

108

A measurement of the neutron to 199Hg magnetic moment ratio  

E-Print Network [OSTI]

The neutron gyromagnetic ratio has been measured relative to that of the 199Hg atom with an uncertainty of 0.8 ppm. We employed an apparatus where ultracold neutrons and mercury atoms are stored in the same volume and report the result $\\gamma_{\\rm n}/\\gamma_{\\rm Hg} = 3.8424574(30)$.

Afach, S; Ban, G; Bison, G; Bodek, K; Burghoff, M; Chowdhuri, Z; Daum, M; Fertl, M; Franke, B; Geltenbort, P; Green, K; van der Grinten, M G D; Grujic, Z; Harris, P G; Heil, W; Hélaine, V; Henneck, R; Horras, M; Iaydjiev, P; Ivanov, S N; Kasprzak, M; Kermaïdic, Y; Kirch, K; Knecht, A; Koch, H -C; Krempel, J; Ku?niak, M; Lauss, B; Lefort, T; Lemière, Y; Mtchedlishvili, A; Naviliat-Cuncic, O; Pendlebury, J M; Perkowski, M; Pierre, E; Piegsa, F M; Pignol, G; Prashanth, P N; Quéméner, G; Rebreyend, D; Ries, D; Roccia, S; Schmidt-Wellenburg, P; Schnabel, A; Severijns, N; Shiers, D; Smith, K F; Voigt, J; Weis, A

2014-01-01T23:59:59.000Z

109

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

110

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

111

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

112

Quantification of the Mercury Adsorption Mechanism on Brominated Activated  

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

Quantification of the Mercury Adsorption Mechanism on Brominated Activated Quantification of the Mercury Adsorption Mechanism on Brominated Activated Carbon Saturday, August 31, 2013 The primary anthropogenic source of mercury (Hg) emissions into the atmosphere is coal-fired power utilities. This work explores materials designed for Hg capture to be applied in the ductwork of a power plant to prevent Hg release into the atmosphere. Bench-scale combustion experiments have been carried out, in which sorbent materials were placed in a simulated flue gas stream doped with ppb levels of Hg. The sorbent surfaces were probed using x-ray absorption spectroscopy to determine the mechanism of Hg binding and to ultimately improve solvent design. The spectroscopy data was analyzed alongside results from density functional theory (DFT) for benchmarking so that DFT can be used as a screening tool for material

113

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

114

Mercury capture in bench-scale absorbers  

SciTech Connect (OSTI)

This paper gives,a brief overview of research being conducted at Argonne National Laboratory on the capture of mercury by both dry sorbents and wet scrubbers. The emphasis in the research is on development of a better understanding of the key factors that control the capture of mercury. Future work is expected to utilize that information for the development of new or modified process concepts featuring enhanced mercury capture capabilities. The results and conclusions to date from the Argonne -research on dry sorbents can be summarized as follows: lime hydrates, either regular or high-surface-area, are `not effective in removing mercury; mercury removals are enhanced by the addition of activated carbon; mercury removals with activated carbon decrease with increasing temperature, larger particle size, and decreasing mercury concentration in the gas; and chemical pretreatment (e.g., with sulfur or (CaCl{sub 2}) can greatly increase the removal capacity of activated carbon. Preliminary results from the wet scrubbing research include: no removal of elemental mercury is obtained under normal scrubber operating conditions; mercury removal is improved by the addition of packing or production of smaller gas bubbles to increase the gas-liquid contact area; polysulfide solutions do not appear promising for enhancing mercury removal in typical FGC systems; stainless steel packing appears to have beneficial properties for mercury removal and should be investigated further; and other chemical additives may offer greatly enhanced removals.

Livengood, C.D.; Huang, H.S.; Mendelsohn, M.H.; Wu, J.M.

1994-08-01T23:59:59.000Z

115

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

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

116

Mercury speciation in floodplain soils and sediments along a contaminated river transect  

SciTech Connect (OSTI)

A novel mercury-specific sequential extraction procedure (SEP) for the assessment of mercury (Hg) speciation in soils and sediments, with emphasis on studying the interaction between Hg and organic matter (OM), was developed and tested. It was applied to determine Hg speciation in floodplain topsoils and surface sediments along the Hg-contaminated part of the river Elbe, and to simultaneously derive some information on the (re)mobilization potentials for Hg from these matrices. The majority of the total Hg in the ecosystem today is bound in the floodplains, which also still geographically reflect the historic emission record. Most of the Hg in both matrices is bound strongly to OM, suggesting low availability. However, distinct differences between Hg speciation in the floodplain soils and sediments were also discovered. Mercury deposited in the floodplains shows speciation patterns that indicate stronger fixation compared with Hg in the sediments. This difference is attributed to the association of Hg with larger quantities of OM, which presumably also has higher molecular weight (MW). By comparison, Hg in the sediments was distributed among weaker binding forms, which are more likely to liberate Hg. Particularly, sediments showed a total lack of sulfidic binding forms for Hg. Pronounced geographical trends were detected in the Hg speciation along the river transect, with a general downstream shift from weaker to stronger binding forms, probably due to increased association with OM. These studies indicate that Hg speciation in riverine ecosystems is dynamic and reflects the chemical mechanisms underlying (bio) geochemical processes like distribution and transport.

Wallschlaeger, D.; Desai, M.V.M.; Spengler, M. [GKSS Forschungszentrum GmbH, Geesthacht (Germany). Inst. fuer Physikalische und Chemische Analytik; Wilken, R.D. [Johannes-Gutenberg-Univ., Mainz (Germany). Inst. of Geosciences

1998-09-01T23:59:59.000Z

117

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

118

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

119

The Origin of the Mercury Bands at 2480A  

Science Journals Connector (OSTI)

The group of eight mercury bands near 2480A was photographed under varied excitation conditions with the purpose of determining their origin. The source was a discharge through mercury vapor produced in a quartz tube through external electrodes by a low-voltage Tesla coil. Five tubes containing distilled mercury and commercial mercury arc lamp showed this group of bands. These bands were weakened by heat along with known mercury bands. The origin is undoubtedly some form of mercury molecule. The most probable forms are Hg2+ and Hg2. Five observations favor Hg2+ over Hg2. (1) These bands have never been observed in fluorescence. (2) The 2476 band is more intense than the 2345 Hg2 band under strong field excitation but weaker than 2345 under low field excitation. (3) No other bands with properties like those of the 2480 group have been observed in the mercury spectrum and Rayleigh has shown that these bands do not occur in absorption. (4) The bands in this group may be classified as sequences v?-v??=0±1±2±3, and a lower limit for D of 0.3 volts estimated. (5) In the v?-v??=0 sequence, emission is observed from state v?=41 indicating molecules with very high vibrational energy. This energy may be supplied by the electric field if the emitter is an ion but not if it is a neutral molecule.

J. Gibson Winans

1932-12-15T23:59:59.000Z

120

Heterobimetallic complexes of gold and mercury. Syntheses and characterizations of Hg sup II (CH sub 2 P(S)Ph sub 2 ) sub 2 (Au sup I Cl) sub 2 and Hg sup II Au sup I (CH sub 2 P(S)Ph sub 2 ) sub 2 Au sup III Cl sub 4  

SciTech Connect (OSTI)

The trinuclear compound Hg{sup II}(CH{sub 2}P(S)Ph{sub 2}){sub 2}(Au{sup I}Cl){sub 2} (2) was synthesized by the reaction of Hg{sup II}(CH{sub 2}P(S)Ph{sub 2}){sub 2} (1) with 2 equiv of Au(THT)Cl (THT = tetrahydrothiophene) in a CH{sub 2}Cl{sub 2} solution. Oxidation of 2 by 1 equiv of C{sub 6}H{sub 5}ICl{sub 2} yielded the mixed-valence trinuclear compound Hg{sup II}Au{sup I}(CH{sub 2}P(S)Ph{sub 2}){sub 2}Au{sup III}Cl{sub 4} (3). The crystal structures of 2 and 3 were determined by single-crystal X-ray diffraction analyses. 2 and 3 have one-dimensional chain structures in the solid. Crystal data: 2, C{sub 26}H{sub 24}HgAu{sub 2}Cl{sub 2}S{sub 2}P{sub 2}{center dot}{sup 1}/{sub 2}C{sub 5}H{sub 12}, space group P{bar 1}, a = 11.930 (4) {angstrom}, b = 13.452 (4) {angstrom}, c = 10.516 (4) {angstrom}, {alpha} = 108.44 (2){degree}, {beta} = 90.61 (3){degree}, {gamma} = 81.06 (2){degree}, V = 1580.1 (8) {angstrom}{sup 3}, Z = 2, R = 0.0432 and R{sub w} = 0.0489 for refinement of 154 least-squares parameters with 2,744 reflections (F{sub {degree}}{sup 2} {ge} 3{sigma}(F{sub {degree}}{sup 2})); 3, C{sub 26}H{sub 24}HgAu{sub 2}Cl{sub 4}S{sub 2}P{sub 2}{center dot}CH{sub 2}Cl{sub 2}, space group P{bar 1}, a = 10.199 (6) {angstrom}, b = 12.340 (3) {angstrom}, c = 15.064 (4) {angstrom}, {alpha} = 74.17 (2){degree}, {beta} = 82.76 (3){degree}, V = 1,799 (1) {angstrom}{sup 3}, Z = 2, R = 0.0505 and R{sub w} = 0.0501 for refinement of 178 least-squares parameters with 1,680 reflections (F{sub 0}{sup 2} {ge} 3{sigma}(F{sub 0}{sup 2})).

Wang, Suning; Fackler, J.P. Jr. (Texas A M Univ., College Station (USA))

1990-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "mercury hg sulfur" 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

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

122

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

123

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.

124

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

125

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

126

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.

127

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

128

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

129

Mercury contaminated sediment sites—An 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

130

Microsoft Word - Hg.doc  

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

The majority of mercury mine wastes at these sites are present as loose, unconsolidated piles, facilitating the transport of mercury-bearing material downstream into...

131

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

132

Mercury mass balance at a wastewater treatment plant employing sludge incineration with offgas mercury control  

Science Journals Connector (OSTI)

Efforts to reduce the deliberate use of mercury (Hg) in modern industrialized societies have been largely successful, but the minimization and control of Hg in waste streams are of continuing importance. Municipal wastewater treatment plants are collection points for domestic, commercial, and industrial wastewaters, and Hg removal during wastewater treatment is essential for protecting receiving waters. Subsequent control of the Hg removed is also necessary to preclude environmental impacts. We present here a mass balance for Hg at a large metropolitan wastewater treatment plant that has recently been upgraded to provide for greater control of the Hg entering the plant. The upgrade included a new fluidized bed sludge incineration facility equipped with activated carbon addition and baghouse carbon capture for the removal of Hg from the incinerator offgas. Our results show that Hg discharges to air and water from the plant represented less than 5% of the mass of Hg entering the plant, while the remaining Hg was captured in the ash/carbon residual stream exiting the new incineration process. Sub-optimum baghouse operation resulted in some of the Hg escaping collection there and accumulating with the ash/carbon particulate matter in the secondary treatment tanks. Overall, the treatment process is effective in removing Hg from wastewater and sequestering it in a controllable stream for secure disposal.

Steven J. Balogh; Yabing H. Nollet

2008-01-01T23:59:59.000Z

133

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

134

The Accelerated Reduction and Elimination of Toxics in Canada: The Case of Mercury-Containing Medical Instruments in Quebec Hospital Centres  

Science Journals Connector (OSTI)

In Canada, medical instruments containing mercury (Hg) are still widely used in hospitals. These are mostly thermometers and sphygmomanometers. Mercury present in these instruments does not in itself constitute a...

P. Guerrier; J.-P. Weber; R. Coté; M. Paul; M. Rhainds

1995-01-01T23:59:59.000Z

135

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

136

NETL: Environmental Research - Characterization of CCBs for Mercury  

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

Characterization of Coal Combustion By-Products for Mercury Characterization of Coal Combustion By-Products for Mercury The objective of this work is to provide the necessary information to assess the impact of controlling Hg from coal-fired utilities by examining the materials resulting from coal combustion, which are either disposed of or utilized. This will be accomplished by: Determining the Hg concentration in coal combustion waste streams, specifically bottom ash, fly ash, flue gas desulfurization sludge and solids (FGDS), and spray dryer solids (SDS) Estimating percentage of Hg collected in the coal combustion waste streams based on the Hg in the as-fired coal Determining if the Hg in the waste and by-product samples is leachable Determining if the Hg in the waste and by-product samples is volatile

137

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

138

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

139

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

140

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

Note: This page contains sample records for the topic "mercury hg sulfur" 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

Field Testing of a Wet FGD Additive for Enhanced Mercury Control  

SciTech Connect (OSTI)

This document is the final report for DOE-NETL Cooperative Agreement DE-FC26-04NT42309, 'Field Testing of a Wet FGD Additive'. The objective of the project has been to demonstrate the use of two flue gas desulfurization (FGD) additives, Evonik Degussa Corporation's TMT-15 and Nalco Company's Nalco 8034, to prevent the re-emission of elemental mercury (Hg{sup 0}) in flue gas exiting wet FGD systems on coal-fired boilers. Furthermore, the project was intended to demonstrate whether such additives can be used to precipitate most of the mercury (Hg) removed in the wet FGD system as a fine salt that can be separated from the FGD liquor and bulk solid byproducts for separate disposal. The project involved pilot- and full-scale tests of the additives in wet FGD absorbers. The tests were intended to determine required additive dosages to prevent Hg{sup 0} re-emissions and to separate mercury from the normal FGD byproducts for three coal types: Texas lignite/Powder 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, Luminant Power (was TXU Generation Company LP), Southern Company, IPL (an AES company), Evonik Degussa Corporation and the Nalco Company. Luminant Power provided the Texas lignite/PRB co-fired test site for pilot FGD tests and project cost sharing. Southern Company provided the low-sulfur Eastern bituminous coal host site for wet scrubbing tests, the pilot- and full-scale jet bubbling reactor (JBR) FGD systems tested, and project cost sharing. IPL provided the high-sulfur Eastern bituminous coal full-scale FGD test site and cost sharing. Evonik Degussa Corporation provided the TMT-15 additive, and the Nalco Company provided the Nalco 8034 additive. Both companies also supplied technical support to the test program as in-kind cost sharing. The project was conducted in six tasks. Of the six tasks, Task 1 involved project planning and Task 6 involved management and reporting. The other four tasks involved field testing on FGD systems, either at pilot or full scale. These four tasks included: 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 Plant Yates; and Task 5 - Full-scale Additive Tests at Plant Yates. The pilot-scale tests were completed in 2005 and the full-scale test using high-sulfur coal was completed in 2006; only the TMT-15 additive was tested in these efforts. The Task 5 full-scale additive tests conducted at Southern Company's Plant Yates Unit 1 were completed in 2007, and both the TMT-15 and Nalco 8034 additives were tested.

Gary Blythe; MariJon Owens

2007-12-31T23:59:59.000Z

142

NETL: Mercury Emissions Control Technologies - Full- Scale Testing of  

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

Full-Scale Testing of Enhanced Mercury Control in Wet FGD Full-Scale Testing of Enhanced Mercury Control in Wet FGD The goal of this project is to commercialize methods for the control of mercury in coal-fired electric utility systems equipped with wet flue gas desulfurization (wet FGD). The two specific objectives of this project are 1) ninety percent (90%) total mercury removal and 2) costs below 1/4 to 1/2 of today's commercially available activated carbon mercury removal technologies. Babcock and Wilcox and McDermott Technology, Inc's (B&W/MTI's) will demonstrate their wet scrubbing mercury removal technology (which uses very small amounts of a liquid reagent to achieve increased mercury removal) at two locations burning high-sulfur Ohio bituminous coal: 1) Michigan South Central Power Agency's (MSCPA) 55 MWe Endicott Station located in Litchfield, Michigan and 2) Cinergy's 1300 MWe Zimmer Station located near Cincinnati, Ohio.

143

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

144

The influence of floodplains on mercury availability  

SciTech Connect (OSTI)

The floodplains of the German river Elbe affect the mercury distribution in the river system in two different ways: they act both as a medium-term sink and as a long-term source. The large amounts of mercury deposited onto the floodplains during annual floodings are first effectively fixed in the soils, rendering them basically unavailable. Sequential extraction experiments reveal that only a small fraction of the mercury (< 3%) is present in available forms, whereas the vast majority is associated with humic substances or present in sulfidic binding forms. After deposition, a small fraction of the total mercury is gradually remobilized into the aqueous phase bound passively to water-soluble humic acids. The availability of mercury in these complexes is still low, since environmental influences such as changes in pH or redox potential and competition with other cations do not cause any mercury liberation. In the next step, reactions in the aqueous phase lead to the formation of the highly available volatile species Hg{sup 0} and dimethylmercury (DMM). Their evaporation gives rise to a strong mercury flux from the floodplains into the atmosphere. Preliminary mass balances indicate that the majority of the deposited mercury stays bound in the floodplain soils, while small amounts are emitted back into the river`s ecosystem. Atmospheric emission is more important as a remobilization pathway than aquatic export.

Wallschlaeger, D.; Wilken, R.D. [GKSS Research Center, Geesthacht (Germany). Inst. of Physical and Chemical Analytics

1997-09-01T23:59:59.000Z

145

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

146

NETL: Health Effects - Risk Assessment of Reduced Mercury Emissions From  

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

Risk Assessment of Reduced Mercury Emissions From Coal-Fired Power Plants Risk Assessment of Reduced Mercury Emissions From Coal-Fired Power Plants Given that mercury emissions from coal power plants will almost certainly be limited by some form of national regulation or legislation, Brookhaven National Laboratory (BNL) is performing an assessment of the reduction in human health risk that may be achieved through reduction in coal plant emissions of mercury. The primary pathway for mercury exposure is through consumption of fish. The most susceptible population to mercury exposure is the fetus. Therefore, the risk assessment focuses on consumption of fish by women of child-bearing age. Preliminary Risk Assessment A preliminary risk assessment was conducted using a simplified approach based on three major topics: Hg emissions and deposition (emphasizing coal plants), Hg consumption through fish, and dose-response functions for Hg. Using information available from recent literature, dose response factors (DRFs) were generated from studies on loss of cognitive abilities (language skills, motor skills, etc.) by young children whose mothers consumed large amounts of fish with high Hg levels. Population risks were estimated for the general population in three regions of the country, (the Midwest, Northeast, and Southeast) that were identified by EPA as being heavily impacted by coal emissions.

147

Microsoft PowerPoint - AWMA2006_Hg Panel_FEELEY.ppt  

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

A&WMA's A&WMA's 99 th Annual Conference & Exhibition Hg Control Technology Panel June 23, 2006 New Orleans, Louisiana Thomas J. Feeley, III thomas.feeley@netl.doe.gov National Energy Technology Laboratory AWMA2006_Hg Panel_FEELEY Outline * Background * Phase II project update/Phase III project descriptions * BOP and related technical issues * Preliminary economic assessment * Byproduct-Hg issues/potential economic impacts * Conclusion AWMA2006_Hg Panel_FEELEY Mercury Control Technology Program Performance/Cost Objectives * Have technologies ready for commercial demonstration by: * 2007 that can reduce "uncontrolled" Hg emissions by 50-70% * 2010 for all coals that can reduce "uncontrolled" Hg emissions by +90% * Reduce cost by 25-50% compared to baseline cost

148

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

149

Field Testing of a Wet FGD Additive for Enhanced Mercury Control - Task 5 Full-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 two flue gas desulfurization (FGD) additives, Evonik Degussa Corporation's TMT-15 and Nalco Company's Nalco 8034, to prevent the re-emission of elemental mercury (Hg{sup 0}) in flue gas exiting wet FGD systems on coal-fired boilers. Furthermore, the project intends to demonstrate whether the additive can be used to precipitate most of the mercury (Hg) removed in the wet FGD system as a fine salt that can be separated from the FGD liquor and bulk solid byproducts for separate disposal. The project is conducting pilot- and full-scale tests of the additives in wet FGD absorbers. The tests are intended to determine required additive dosages to prevent Hg{sup 0} re-emissions and to separate mercury from the normal FGD byproducts for three coal types: Texas lignite/Powder 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, Luminant Power (was TXU Generation Company LP), Southern Company, IPL (an AES company), Evonik Degussa Corporation and the Nalco Company. Luminant Power has provided the Texas lignite/PRB co-fired test site for pilot FGD tests and cost sharing. Southern Company has provided 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 tested. IPL provided the high-sulfur Eastern bituminous coal full-scale FGD test site and cost sharing. Evonik Degussa Corporation is providing the TMT-15 additive, and the Nalco Company is providing the Nalco 8034 additive. Both companies are also supplying technical support to the test program as in-kind cost sharing. 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 Plant Yates; and Task 5 - Full-scale Additive Tests at Plant Yates. The pilot-scale tests and the full-scale test using high-sulfur coal were completed in 2005 and 2006 and have been previously reported. This topical report presents the results from the Task 5 full-scale additive tests, conducted at Southern Company's Plant Yates Unit 1. Both additives were tested there.

Gary Blythe; MariJon Owens

2007-12-01T23:59:59.000Z

150

FIELD TEST PROGRAM TO DEVELOP COMPREHENSIVE DESIGN, OPERATING, AND COST DATA FOR MERCURY CONTROL SYSTEMS  

SciTech Connect (OSTI)

PG&E NEG Salem Harbor Station Unit 1 was successfully tested for applicability of activated carbon injection as a mercury control technology. Test results from this site have enabled a thorough evaluation of mercury control at Salem Harbor Unit 1, including performance, estimated cost, and operation data. This unit has very high native mercury removal, thus it was important to understand the impacts of process variables on native mercury capture. The team responsible for executing this program included plant and PG&E headquarters personnel, EPRI and several of its member companies, DOE, ADA, Norit Americas, Inc., Hamon Research-Cottrell, Apogee Scientific, TRC Environmental Corporation, Reaction Engineering, as well as other laboratories. The technical support of all of these entities came together to make this program achieve its goals. Overall the objectives of this field test program were to determine the mercury control and balance-of-plant impacts resulting from activated carbon injection into a full-scale ESP on Salem Harbor Unit 1, a low sulfur bituminous-coal-fired 86 MW unit. It was also important to understand the impacts of process variables on native mercury removal (>85%). One half of the gas stream was used for these tests, or 43 MWe. Activated carbon, DARCO FGD supplied by NORIT Americas, was injected upstream of the cold side ESP, just downstream of the air preheater. This allowed for approximately 1.5 seconds residence time in the duct before entering the ESP. Conditions tested in this field evaluation included the impacts of the Selective Non-Catalytic Reduction (SNCR) system on mercury capture, of unburned carbon in the fly ash, of adjusting ESP inlet flue gas temperatures, and of boiler load on mercury control. The field evaluation conducted at Salem Harbor looked at several sorbent injection concentrations at several flue gas temperatures. It was noted that at the mid temperature range of 322-327 F, the LOI (unburned carbon) lost some of its ability to capture vapor phase Hg, however activated carbon performed relatively well. At the normal operating temperatures of 298-306 F, mercury emissions from the ESP were so low that both particulate and elemental mercury were ''not detected'' at the detection limits of the Ontario Hydro method for both baseline and injection tests. The oxidized mercury however, was 95% lower at a sorbent injection concentration of 10 lbs/MMacf compared with baseline emissions. When the flue gas temperatures were increased to a range of 343-347 F, mercury removal efficiencies were limited to <25%, even at the same sorbent injection concentration. Other tests examined the impacts of fly ash LOI, operation of the SNCR system, and flue gas temperature on the native mercury capture without sorbent injection. Listed below are the main conclusions from this program: (1) SNCR on/off test showed no beneficial effect on mercury removal caused by the SNCR system. (2) At standard operating temperatures ({approx} 300 F), reducing LOI from 30-35% to 15-20% had minimal impact on Hg removal. (3) Increasing flue gas temperatures reduced Hg removal regardless of LOI concentrations at Salem Harbor (minimum LOI was 15%). Native mercury removal started to fall off at temperatures above 320 F. ACI effectiveness for mercury removal fell off at temperatures above 340 F. (4) Test method detection limits play an important role at Salem Harbor due to the low residual emissions. Examining the proposed MA rule, both the removal efficiency and the emission concentrations will be difficult to demonstrate on an ongoing basis. (5) Under tested conditions the baseline emissions met the proposed removal efficiency for 2006, but not the proposed emission concentration. ACI can meet the more-stringent 2012 emission limits, as long as measurement detection limits are lower than the Ontario Hydro method. SCEM testing was able to verify the low emissions. For ACI to perform at this level, process conditions need to match those obtained during testing.

Michael D. Durham

2004-10-01T23:59:59.000Z

151

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

152

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

153

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

154

Mercury Control Technologies for Electric Utilities Burning Lignite Coal  

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

Mercury control technologies for Mercury control technologies for electric utilities Burning lignite coal Background In partnership with a number of key stakeholders, the U.S. Department of Energy's Office of Fossil Energy (DOE/FE), through its National Energy Technology Laboratory (NETL), has been carrying out a comprehensive research program since the mid-1990s focused on the development of advanced, cost-effective mercury (Hg) control technologies for coal-fired power plants. Mercury is a poisonous metal found in coal, which can be harmful and even toxic when absorbed from the environment and concentrated in animal tissues. Mercury is present as an unwanted by-product of combustion in power plant flue gases, and is found in varying percentages in three basic chemical forms(known as speciation): particulate-bound mercury, oxidized

155

Geological and Anthropogenic Factors Influencing Mercury Speciation in Mine  

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

Geological and Anthropogenic Factors Influencing Mercury Speciation Geological and Anthropogenic Factors Influencing Mercury Speciation in Mine Wastes Christopher S. Kim,1 James J. Rytuba,2 Gordon E. Brown, Jr.3 1Department of Physical Sciences, Chapman University, Orange, CA 92866 2U.S. Geological Survey, Menlo Park, CA 94025 3Department of Geological and Environmental Sciences, Stanford University, Stanford, CA 94305 Introduction Figure 1. Dr. Christopher Kim collects a mine waste sample from the Oat Hill mercury mine in Northern California. The majority of mercury mine wastes at these sites are present as loose, unconsolidated piles, facilitating the transport of mercury-bearing material downstream into local watersheds. Mercury (Hg) is a naturally occurring element that poses considerable health risks to humans, primarily through the consumption of fish which

156

Final disposal options for mercury/uranium mixed wastes from the Oak Ridge Reservation  

SciTech Connect (OSTI)

Laboratory testing was completed on chemical stabilization and physical encapsulation methods that are applicable (to comply with federal and state regulations) to the final disposal of both hazardous and mixed hazardous elemental mercury waste that is in either of the following categories: (1) waste generated during decontamination and decommissioning (D and D) activities on mercury-contaminated buildings, such as Building 9201-4 at the Oak Ridge Y-12 Plant, or (2) waste stored and regulated under either the Federal Facilities Compliance Agreement or the Federal Facilities Compliance Act. Methods were used that produced copper-mercury, zinc-mercury, and sulfur-mercury materials at room temperature by dry mixing techniques. Toxicity Characteristic Leaching Procedure (TCLP) results for mercury on batches of both the copper-mercury and the sulfur-mercury amalgams consistently produced leachates with less than the 0.2-mg/L Resource Conservation and Recovery Act (RCRA) regulatory limit for mercury. The results clearly showed that the reaction of mercury with sulfur at room temperature produces black mercuric sulfide, a material that is well suited for land disposal. The results also showed that the copper-mercury and zinc-mercury amalgams had major adverse properties that make them undesirable for land disposal. In particular, they reacted readily in air to form oxides and liberate elemental mercury. Another major finding of this study is that sulfur polymer cement is potentially useful as a physical encapsulating agent for mercuric sulfide. This material provides a barrier in addition to the chemical stabilization that further prevents mercury, in the form of mercuric sulfide, from migrating into the environment.

Gorin, A.H.; Leckey, J.H.; Nulf, L.E.

1994-08-29T23:59:59.000Z

157

The mission of the Remediation of Mercury and Industrial  

Broader source: Energy.gov (indexed) [DOE]

Remediation of Mercury and Industrial Remediation of Mercury and Industrial Contaminants Applied Field Research Initiative is to control the flux of contaminants in soil and water environments for the purpose of protecting surface water, groundwater, and ecological receptors. For more information, contact: Eric Pierce Oak Ridge National Laboratory 1 Bethel Valley Road, MS 6038 Oak Ridge, TN 37831 pierceem@ornl.gov (865) 574-9968 Kurt Gerdes DOE-EM Office of Groundwater and Soil Remediation kurt.gerdes@em.doe.gov (301) 903-7289 Sediment Biota Groundwater Flow Fluctuating Water Table Hg in building structures and rubble Waterborne mercury (mercury being transported via water being released from the facilities to the creeks) Hg currently present in the creek and sediments along the base of the creek

158

DOE-NETLs Mercury R&D Program  

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

U.S. Department of Energy's U.S. Department of Energy's Mercury Control Technology Phase II Field Testing Program Mercury Experts' Conference 2 May 24-25, 2005 Ottawa, Canada Thomas J. Feeley, III thomas.feeley@netl.doe.gov National Energy Technology Laboratory SEC Meeting June 2005 Mercury Control Technology Field Testing Program Performance/Cost Objectives * Have technologies ready for commercial demonstration by 2007 for all coals * Reduce "uncontrolled" Hg emissions by 50-70% * Reduce cost by 25-50% compared to baseline cost estimates Baseline Costs: $50,000 - $70,000 / lb Hg Removed 2000 Year Cost SEC Meeting June 2005 Stages of Mercury Control Technology Development DOE RD&D Model Lab/Bench/Pilot-Scale Testing Field Testing (Slip Stream/Full Scale) 1993 1999-2000 2007-2010 2012-2015

159

Mercury Monohalides: Suitability for Electron Electric Dipole Moment Searches  

E-Print Network [OSTI]

Heavy polar diatomic molecules are the primary tools for searching for the T-violating permanent electric dipole moment of the electron (eEDM). Valence electrons in some molecules experience extremely large effective electric fields due to relativistic interactions. These large effective electric fields are crucial to the success of polar-molecule-based eEDM search experiments. Here we report on the results of relativistic ab initio calculations of the effective electric fields in a series of molecules that are highly sensitive to an eEDM, the mercury monohalides (HgF, HgCl, HgBr,and HgI). We study the influence of the halide anions on effective electric field, and identify HgBr and HgI as interesting candidates for future electric dipole moment search experiments.

Prasannaa, V S; Abe, M; Das, B P

2014-01-01T23:59:59.000Z

160

Mercury Source Zone Identification using Soil Vapor Sampling and Analysis  

SciTech Connect (OSTI)

Development and demonstration of reliable measurement techniqes that can detect and help quantify the nature and extent of elemental mercury (Hg(0)) in the subsurface are needed to reduce certainties in the decision making process and increase the effectiveness of remedial actions. We conducted field tests at the Y-12 National Security Complex (NSC) in Oak Ridge, TN, to determine if sampling and analysis of Hg(0) vapors in the shallow subsurface (<0.3 m depth) can be used to as an indicator of the location and extent of Hg(0) releases in the subsurface. We constructed a rigid PVC pushprobe assembly, which was driven into the ground. Soil gas samples were collected through a sealed inner tube of the assembly and analyzed immediately in the field with a Lumex and/or Jerome Hg(0) analyzer. Time-series sampling showed that Hg vapor concentrations were fairly stable over time suggesting that the vapor phase Hg(0) was not being depleted and that sampling results were not dependent on the soil gas purge volume. Hg(0) vapor data collected at over 200 pushprobe locations at 3 different release sites correlated well to areas of known Hg(0) contamination. Vertical profiling of Hg(0) vapor concentrations conducted at 2 locations provided information on the vertical distribution of Hg(0) contamination in the subsurface. We concluded from our studies that soil gas sampling and analysis can be conducted rapidly and inexpensively at a large scale to help identify areas contaminated with Hg(0).

Watson, David B [ORNL] [ORNL; Miller, Carrie L [ORNL] [ORNL; Lester, Brian P [ORNL] [ORNL; Lowe, Kenneth Alan [ORNL] [ORNL; Southworth, George R [ORNL] [ORNL; Bogle, Mary Anna [ORNL] [ORNL; Liang, Liyuan [ORNL] [ORNL; Pierce, Eric M [ORNL] [ORNL

2014-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "mercury hg sulfur" 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.


161

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.

162

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

163

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

164

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

165

A Critical Review on the Heterogeneous Catalytic Oxidation of Elemental Mercury in Flue Gases  

E-Print Network [OSTI]

of novel and highly efficient Hg0 oxidation catalysts. 1. INTRODUCTION Mercury is a leading concern among. Exposure to high levels of mercury has been associated with serious neurological and developmental effects to tremors, inability to walk, convulsions, and death.1,2 Coal-fired utility boilers, which release more than

Guo, John Zhanhu

166

Complexation of mercury by dissolved organic matter in surface waters of Galveston Bay, Texas  

Science Journals Connector (OSTI)

The chemical speciation of dissolved mercury in surface waters of Galveston Bay was determined using the concentrations of mercury-complexing ligands and conditional stability constants of mercury-ligand complexes. Two classes of natural ligands associated with dissolved organic matter were determined by a competitive ligand exchange-solvent solvent extraction (CLE-SSE) method: a strong class (Ls), ranging from 19 to 93 pM with an average conditional stability constant (KHgLs) of 1028, and a weak class (Lw) ranging from 1.4 to 9.8 nM with an average \\{KHgLs\\} of 1023. The range of conditional stability constants between mercury and natural ligands suggested that sulfides and thiolates are important binding sites for dissolved mercury in estuarine waters. A positive correlation between the estuarine distribution of dissolved glutathione and that of mercury-complexing ligands supported this suggestion. Thermodynamic equilibrium modeling using stability constants for HgL, HgClx, Hg(OH)x, and HgCl(OH) and concentrations of each ligand demonstrated that almost all of the dissolved mercury (> 99%) in Galveston Bay was complexed by natural ligands associated with dissolved organic matter. The importance of low concentrations of high-affinity ligands that may originate in the biological system (i.e., glutathione and phytochelatin) suggests that the greater portion of bulk dissolved organic matter may not be important for mercury complexation in estuarine surface waters.

Seunghee Han; Gary A. Gill; Ronald D. Lehman; Key-Young Choe

2006-01-01T23:59:59.000Z

167

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

168

Chemical and physical speciation of mercury in Offatts Bayou: A seasonally anoxic bayou in Galveston Bay  

SciTech Connect (OSTI)

A chemical equilibrium model was used to predict the solution speciation of dissolved mercury (Hg) in the stratified water column of Offatts Bayou, a subestuary in Galveston Bay, Texas, which undergoes seasonal anoxia in bottom waters. Chemical equilibrium modeling was conducted using conditional stability constants and concentrations of Hg-complexing organic ligands experimentally determined by competitive ligand equilibration methods. Dissolved Hg complexation was dominated by interactions with sulfide and dissolved organic matter (DOM) (HOHgHS0, HOHgHS(DOM), HgSHS2, and HgS 2{ 2 ) at all depths. Sulfide and glutathione competed for methylmercury (MeHg) complexation in oxic layers; in anoxic waters, sulfide complexation dominated MeHg speciation. The particle–water distribution coefficient (Kd) of Hg decreased in the anoxic layer of the water column, where the dissolved sulfide concentration increased, providing evidence that sulfide complexation influences the solubility of Hg. The solubility of MeHg was elevated in the anoxic as compared to the oxic layers, and this distributional feature was coincident with a change in the solution speciation of dissolved MeHg from glutathione/sulfide complexation in the oxic layers to a predominantly sulfide complexation in the anoxic layers. Maximum enrichment of Hg, MeHg, and iron (Fe) in suspended particulate matter was observed in the lower layer of the pycnocline, most likely resulting from formation of insoluble Fe oxide, which scavenged dissolved Hg sulfide and MeHg-sulfide species. The concomitant decrease in dissolved inorganic Hg, Fe, and sulfide in the anoxic layers is suggested to result from scavenging of inorganic Hg by FeS, which is in accordance with the Hg speciation model. Overall, Hg cycling in the water column of Offatts Bayou was associated with sulfide and DOM complexation, Fe dissolution/precipitation, water column production of MeHg, and/or efflux of MeHg from anoxic sediment.

Han, Seunghee; Lehman, Ronald D.; Choe, Key-Young; Gill, Gary A.

2007-07-01T23:59:59.000Z

169

Use of advanced cluster analysis to characterize seafood consumption patterns and methyle mercury exposures among  

E-Print Network [OSTI]

1 N° 2007/14 Use of advanced cluster analysis to characterize seafood consumption patterns. This study provides demonstrates that a global increase in seafood consumption could lead to MeHg exposure exclusively from eating fish and seafood products. Of the organic mercury compounds, MeHg is the most toxic

Paris-Sud XI, Université de

170

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

171

Mechanistic Investigation of Mercury Sorption by Brazilian Pepper Biochars of Different Pyrolytic Temperatures Based on Xray  

E-Print Network [OSTI]

Mechanistic Investigation of Mercury Sorption by Brazilian Pepper Biochars of Different Pyrolytic, United States *S Supporting Information ABSTRACT: We investigated the mechanisms of Hg sorption onto different analytical techniques. The Hg sorption capacity of BP300, BP450, and BP600 was 24.2, 18.8, and 15

Ma, Lena

172

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, Jožef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)] [Department of Environmental Sciences, Jožef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia); Ogrinc, Nives, E-mail: nives.orginc@ijs.si [Department of Environmental Sciences, Jožef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)] [Department of Environmental Sciences, Jožef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia); Kotnik, Jože, E-mail: joze.kotnik@ijs.si [Department of Environmental Sciences, Jožef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)] [Department of Environmental Sciences, Jožef 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); Žagar, Dušan, 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, Jožef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)] [Department of Environmental Sciences, Jožef Stefan Institute, Jamova 39, 1000 Ljubljana (Slovenia)

2013-08-15T23:59:59.000Z

173

MERCURY EXCESS  

Science Journals Connector (OSTI)

Congress and EPA probe possibility of long-term STORAGE of liquid metal CHERYL HOGUE, C&EN WASHINGTON ... Hazardous waste handlers keep mercury from polluting the environment by reclaiming the liquid metal from scrap electrical switches, thermometers, and fluorescent light bulbs. ...

2007-07-02T23:59:59.000Z

174

NETL: Mercury Emissions Control Technologies - Preliminary Field Evaluation  

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

Preliminary Field Evaluation of Mercury Control Using Combustion Modifications Preliminary Field Evaluation of Mercury Control Using Combustion Modifications General Electric – Energy and Environmental Research Corporation is developing a new technology that reduces the cost of mercury removal from flue gas by combining it with carbon reduction in a burnout system and simultaneously controlling nitrogen oxides emissions. Data on mercury removal at Western Kentucky Electric’s Green Station will be obtained and used to assess options to improve the efficiency of mercury removal. These options will be further investigated in pilot-scale testing on a 300 kW combustor. Related Papers and Publications: Preliminary Field Evaluation of Hg Control Using Combustion Modifications [PDF-732KB] - Presented at the 2004 Electric Utilities Environmental Conference, Tucson, AZ - January 19-22, 2004.

175

Catalysts for Oxidation of Mercury in Flue Gas  

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

Catalysts for Oxidation of Mercury in Flue Gas Catalysts for Oxidation of Mercury in Flue Gas Opportunity The Department of Energy's National Energy Technology Laboratory (NETL) is seeking licensing partners interested in implementing United States Patent Number 7,776,780 entitled "Catalysts for Oxidation of Mercury in Flue Gas." Disclosed in this patent are catalysts for the oxidation of elemental mercury in flue gas. These novel catalysts include iridium (Ir), platinum/iridium (Pt/Ir), and Thief carbons. The catalyst materials will adsorb the oxidizing agents HCl, Cl 2 , and other halogen species in the flue gas stream that are produced when fuel is combusted. These adsorbed oxidizing agents can then react with elemental mercury in the stream, which is difficult to capture, and oxidize it to form Hg (II) species,

176

NETL: Mercury Emissions Control Technologies - University of North Dakota,  

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

Table Of Contents for Field Testing Enhancing Carbon Reactivity in Mercury Control in Lignite-Fired Systems Mercury Oxidation Upstream of an ESP and Wet FGD Enhancing Carbon Reactivity in Mercury Control in Lignite-Fired Systems The scope of the project consists of attempting to control mercury at four different power plants using two novel concepts. The first concept is using furnace additives that will enhance the sorbent effectiveness for mercury capture. The other concept involves using novel treated carbons to significantly increase sorbent reactivity and resultant capture of Hg. The furnace additives will be tested at Leland Olds Station and Antelope Valley Station while the novel sorbents will be tested at Stanton Station Units 1 &10. Related Papers and Publications:

177

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

178

How humic substances dominate mercury geochemistry in contaminated floodplain soils and sediments  

SciTech Connect (OSTI)

The interaction of mercury (Hg) and humic substances (hs) was studied in floodplain topsoils and surface sediments of the contaminated German river Elbe. An intimate coupling exists between the geochemical cycles of Hg and organic carbon (OC) in this ecosystem. Humic substances exert a dominant influence on several important parallel geochemical pathways of Hg, including binding, transformation, and transport processes. Significant differences exist between the Hg-hs associations in floodplains and sediments. Both humic acids (ha) and fulvic acids (fa) contribute to Hg binding in the sediments. In contrast, ultrafiltration experiments proved that Hg in the floodplain soils is almost exclusively bound to very large humic acids (ha) with a nominal molecular weight (MW) > 300,000. Successive cation and anion exchange experiments demonstrated that those Hg-ha complexes are inert toward competition by other cations, and also apparently predominantly electroneutral. Speciation transformation reactions in the solid phase were investigated by sequential extraction and thermal release experiments. Upon addition of Hg model compounds to a sediment matrix, all species were transformed to the same new speciation pattern, regardless of their original speciation. The accompanying alterations in availability and solubility were partially due to interconversion between the different Hg redox states, including Hg(I). Simultaneously, partial transformation of added Hg{sup 2+} into volatile Hg compounds (35% in 10 d) was observed. Finally, Hg association with water-soluble ha continuously increased downstream, indicating that hs play a key role in both lateral and longitudinal Hg transport in the Elbe ecosystem.

Wallschlaeger, D.; Desai, M.V.M.; Spengler, M.; Windmoeller, C.C.; Wilken, R.D. [GKSS Forschungszentrum GmbH, Geesthacht (Germany). Inst. fuer Physikalische und Chemische Analytik

1998-09-01T23:59:59.000Z

179

An Approach to Problems of a Geothermal Mercury Survey, Puna, Hawaii | Open  

Open Energy Info (EERE)

Approach to Problems of a Geothermal Mercury Survey, Puna, Hawaii Approach to Problems of a Geothermal Mercury Survey, Puna, Hawaii Jump to: navigation, search OpenEI Reference LibraryAdd to library Journal Article: An Approach to Problems of a Geothermal Mercury Survey, Puna, Hawaii Abstract Concentrations of soil mercury of 15 to 1250ppb were determined in the Puna geothermal areaon the lower east rift zone of Kilauea volcano. As the area is young and volcanically active a wide range of soils exist. Hg concentrations are partly controlled by such factors as soil development and organic content, which tend to complicate interpretation of the absolute concentrations measured. The pH of both ground gas and soil may also influence transport and fixation of the Hg, and some low pH soils may be due to SO2 and C02 in ground gas. By relating the Hg concentration of

180

Summary - Mitigation and Remediation of Mercury Contamination at the Y-12 Plant, Oak Ridge, TN  

Broader source: Energy.gov (indexed) [DOE]

Oak Ridge, TN Oak Ridge, TN EM Project: Mitigation/Remediation of Hg ETR Report Date: April 2008 ETR-13 United States Department of Energy Office of Environmental Management (DOE-EM) External Technical Review of the Mitigation and Remediation of Mercury Contamination at the Y-12 Plant, Oak Ridge, TN Why DOE-EM Did This Review From 1953 to 1983, ~240,000 pounds of mercury (Hg) were released to the East Fork Popular Creek during the operation of the Y-12 Plant. In 1963, direct systematic releases of mercury stopped; however, mercury continues to be released into the creek from various sources of contamination in the Y-12 complex. Remediation completed up to 1992 resulted in an overall reduction of Hg loading from 150 g/day in 1983 to 15 g/day in 1992, with a

Note: This page contains sample records for the topic "mercury hg sulfur" 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

Characterization of isothermal vapor phase epitaxial (Hg,Cd)Te  

Science Journals Connector (OSTI)

We report on the characterization of mercury cadmium telluride (Hg 1?x Cd x Te) film grown by the isothermal vapor phase epitaxial method (ISOVPE) and on the surface conversion of bulk Hg 1?xCd x Te to larger bandgap material. The crystal perfection is evaluated using defect etching electron beam and electrolyte electroreflectance (EBER and EER) and Rutherford backscattering spectrometry (RBS). Hall measurements are used to measure carrier densities and mobilities. Surface concentrations and concentration profiles are measured for the ISOVPE grown layers by transmission Fourier transform infrared spectroscopy (FTIR) and electron?probe microanalysis (EPMA) to establish quantitative informations about composition control. Metal–insulator?semiconductor (MIS) structures were made and the properties important to device performance such as compositional uniformity storage time and carrier concentration are measured. The ISOVPE layers are compared in quality to films grown by other methods and show promise for MIS devices.

S. B. Lee; L. K. Magel; M. F. S. Tang; D. A. Stevenson; J. H. Tregilgas; M. W. Goodwin; R. L. Strong

1990-01-01T23:59:59.000Z

182

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

183

Geochemical, Genetic, and Community Controls on Mercury  

SciTech Connect (OSTI)

The sulfate-reducing bacteria (SRB) are soil bacteria that share two common characteristics, strict anaerobiosis and the ability to respire sulfate. The metabolic activities of these bacteria play significant roles in the global sulfur cycle, anaerobic degradation of biomass, biological metal corrosion in the environment and, recently, degradation of toxic compounds. The accumulation of evidence suggests these bacteria are also key to the production of the neurotoxin methylmercury in environmental settings. We propose to use our experience with the development of genetics in sulfate-reducing bacteria of the genus Desulfovibrio to create mutations that will eliminate the methylation of mercury, thereby identifying the genes essential for this process. This information may allow the environmental monitoring of the mercury methylation potential to learn the location and quantity of the production this toxin. From these data, more accurate predictive models of mercury cycling can be generated.

Wall, Judy D.

2014-11-10T23:59:59.000Z

184

"Seeing" Mercury Methylation in Progress  

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

Mercury in the environment can easily reach toxic levels. In a process called methylation, Hg is transformed into a form that can be accumulated in the muscle and fatty tissue of fish. Accumulated levels of methylmercury become higher as the fish grow, and levels are magnified up the food web as larger fish eat smaller fish, a process called biomagnification. As a result, mercury concentrations in fish can be millions of times higher than in surrounding waters [1]. Fish advisories have been set to limit consumption of certain fish higher up on the food web, especially for pregnant women and small children (see Figure 1). Mercury in the environment can easily reach toxic levels. In a process called methylation, Hg is transformed into a form that can be accumulated in the muscle and fatty tissue of fish. Accumulated levels of methylmercury become higher as the fish grow, and levels are magnified up the food web as larger fish eat smaller fish, a process called biomagnification. As a result, mercury concentrations in fish can be millions of times higher than in surrounding waters [1]. Fish advisories have been set to limit consumption of certain fish higher up on the food web, especially for pregnant women and small children (see Figure 1). figure 1 Figure 1. Mercury health risks Health advisory from the CALFED Science Program to limit consumption of fish, in order to avoid excessive accumulation of Hg. Methylated Hg is biomagnified up the food chain, attaining high levels in some types of sportfish. http://science.calwater.ca.gov/images/scinews_hg_da_lg.jpg

185

Catalyst Additives to Enhance Mercury Oxidation and Capture  

SciTech Connect (OSTI)

Preliminary research has shown that SCR catalysts employed for nitrogen-oxide reduction can effectively oxidize mercury. This report discusses initial results from fundamental investigations into the behavior of mercury species in the presence of SCR catalysts at Southern Research Institute. Three different SCR catalysts are being studied. These are honeycomb-type, plate-type, and a hybrid-type catalyst. The catalysts are manufactured and supplied by Cormetech Inc., Hitachi America Ltd., and Haldor-Topsoe Inc., respectively. Test methods and experimental procedures were developed for current and future testing. The methods and procedures equalize factors influencing mercury adsorption and oxidation (surface area, catalyst activity, and pore structure) that normally differ for each catalyst type. Initial testing was performed to determine the time necessary for each catalyst to reach surface-adsorption equilibrium. In addition, the fraction of Hg oxidized by each of the SCR catalyst types is being investigated, for a given amount of catalyst and flow rate of mercury and flue gas. The next major effort will be to examine the kinetics of mercury oxidation across the SCR catalysts with respect to changes in mercury concentration and with respect to HCl concentration. Hg-sorption equilibrium times will also be investigated with respect to ammonia concentration in the simulated flue gas.

Jared W. Cannon; Thomas K. Gale

2004-12-31T23:59:59.000Z

186

Mercury oxidation over a vanadia-based selective catalytic reduction catalyst  

SciTech Connect (OSTI)

The process of the reaction among elemental mercury (Hg{sup 0}) and reactive flue gas components across the selective catalytic reduction (SCR) catalyst was studied in a laboratory-scale reactor. Prepared vanadia-based SCR catalysts were characterized and analyzed to understand the potential reaction pathways. Mercury oxidation was observed when pro-exposure of the SCR catalyst to HCl, followed by passing through Hg{sup 0}/N{sub 2} in the absence of gas-phase HCl. At testing conditions, Hg{sup 0} was found to desorb from the catalyst surface by adding HCl to the gas stream, which implies that HCl adsorption onto the SCR catalyst is strong relative to the mercury. Surface analysis verified the absorption of HCl onto the SCR catalysts, and the potential reaction pathways were proposed. Indeed, the monomeric vanadyl sites on the catalyst surface were found to be responsible for the adsorption of both Hg{sup 0} and HCl, which means they are active for mercury oxidation. Furthermore, the detailed Langmuir-Hinshelwood mechanism was proposed to explain the mercury oxidation on the SCR catalyst, where reactive Cl generated from adsorbed HCl reacts with adjacent Hg{sup 0}. 44 refs., 10 figs.

Sheng He; Jinsong Zhou; Yanqun Zhu; Zhongyang Luo; Mingjiang Ni; Kefa Cen [Zhejiang University, Hangzhou (China). State Key Laboratory of Clean Energy Utilization

2009-01-15T23:59:59.000Z

187

Atmospheric Deposition of Mercury and Methylmercury to Landscapes and Waterbodies of the Athabasca Oil Sands Region  

Science Journals Connector (OSTI)

Mercury (Hg) is of particular interest as methylmercury (MeHg), a neurotoxin which bioaccumulates through foodwebs, can reach levels in fish and wildlife that may pose health risks to human consumers. ... Relationships between Hg and numerous parameters, including natural environmental factors such as snowpack characteristics and wind, as well as other chemicals, were examined to identify potential factors driving the spatial patterns in Hg deposition to the oil sands region. ... Predominant winds in the Alberta oil sands region are generally from the east, southwest, and northwest (Table S5, Figure S8). ...

Jane L. Kirk; Derek C. G. Muir; Amber Gleason; Xiaowa Wang; Greg Lawson; Richard A. Frank; Igor Lehnherr; Fred Wrona

2014-05-29T23:59:59.000Z

188

Assessment of mercury in the Savannah River Site environment  

SciTech Connect (OSTI)

Mercury has been valued by humans for several millennia. Its principal ore, cinnabar, was mined for its distinctive reddish-gold color and high density. Mercury and its salts were used as medicines and aphrodisiacs. At SRS, mercury originated from one of the following: as a processing aid in aluminum dissolution and chloride precipitation; as part of the tritium facilities` gas handling system; from experimental, laboratory, or process support facilities; and as a waste from site operations. Mercury is also found in Par Pond and some SRS streams as the result of discharges from a mercury-cell-type chlor-alkali plant near the city of Augusta, GA. Reactor cooling water, drawn from the Savannah River, transported mercury onto the SRS. Approximately 80,000 kg of mercury is contained in the high level waste tanks and 10,000 kg is located in the SWDF. Additional quantities are located in the various seepage basins. In 1992, 617 wells were monitored for mercury contamination, with 47 indicating contamination in excess of the 0.002-ppm EPA Primary Drinking Water Standard. More than 20 Savannah River Ecology Laboratory (SREL) reports and publications pertinent to mercury (Hg) have been generated during the last two decades. They are divided into three groupings: SRS-specific studies, basic studies of bioaccumulation, and basic studies of effect. Many studies have taken place at Par Pond and Upper Three Runs Creek. Mercury has been detected in wells monitoring the groundwater beneath SRS, but not in water supply wells in excess of the Primary Drinking Water Limit of 0.002 ppm. There has been no significant release of mercury from SRS to the Savannah River. While releases to air are likely, based on process knowledge, modeling of the releases indicates concentrations that are well below the SCDHEC ambient standard.

Kvartek, E.J.; Carlton, W.H.; Denham, M.; Eldridge, L.; Newman, M.C.

1994-09-01T23:59:59.000Z

189

Field Demonstration of Enhanced Sorbent Injection for Mercury Control  

SciTech Connect (OSTI)

Alstom Power Inc. has conducted a DOE/NETL-sponsored program (under DOE Cooperative Agreement No. DE-FC26-04NT42306) to demonstrate Mer-Cure{trademark}, one of Alstom's mercury control technologies for coal-fired boilers. Mer-Cure{trademark} utilizes a small amount of Mer-Clean{trademark} sorbent that is injected into the flue gas stream for oxidation and adsorption of gaseous mercury. Mer-Clean{trademark} sorbents are carbon-based and prepared with chemical additives that promote oxidation and capture of mercury. Mer-Cure{trademark} is unique in that the sorbent is injected into an environment where the mercury capture kinetics is accelerated. This full-scale demonstration program was comprised of three seven-week long test campaigns at three host sites including PacifiCorp's 240-MW{sub e} Dave Johnston Unit No.3 burning a Powder River Basin (PRB) coal, Basin Electric's 220-MW{sub e} Leland Olds Unit No.1 burning a North Dakota lignite, and Reliant Energy's 170-MW{sub e} Portland Unit No.1 burning an Eastern bituminous coal. All three boilers are equipped with electrostatic precipitators. The goals for this Round 2 program, established by DOE/NETL under the original solicitation, were to reduce the uncontrolled mercury emissions by 50 to 70% at a cost 25 to 50% lower than the previous target of $60,000/lb mercury removed. The results for all three host sites indicated that Mer-Cure{trademark} technology could achieve mercury removal of 90%. The estimated mercury removal costs were 25-92% lower than the benchmark of $60,000/lb mercury removed. The estimated costs for control, at sorbent cost of $1.25 to $2.00/lb respectively, are as follows: (1) Dave Johnston Unit No.3--$2,650 to $4,328/lb Hg removed (92.8% less than $60k/lb); (2) Leland Olds Unit No.1--$8,680 to $13,860/lb Hg removed (76.7% less than $60k/lb); and (3) Portland Unit No.1--$28,540 to $45,065/lb Hg removed (24.9% less than $60k/lb). In summary, the results from demonstration testing at all three host sites show that the goals established by DOE/NETL were exceeded during this test program. Mercury removal performance4 of greater than 90% reduction was above the 50-70% reduction goal, and mercury removal cost of 25-92% lower than the benchmark was above the 25 to 50% cost reduction goal.

Shin Kang; Robert Schrecengost

2009-01-07T23:59:59.000Z

190

XAS Catches the Chemical Form of Mercury in Fish  

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

view large image view large image contact info Friday, 29 August 2003 X-ray Absorption Spectroscopy Catches the Chemical Form of Mercury in Fish - SSRL Scientists Reveal New Findings in Science Article The presence of "methyl mercury" in fish is well-known, but until now the detailed chemical identity of the mercury has remained a mystery. In an x-ray absorption spectroscopy study published in the August 29 issue of Science (Science 301, 2003: 1203; Science now: Murky Picture on Fish Mercury), SSRL scientists report that the chemical form of mercury involves a sulfur atom (most likely in a so-called aliphatic form). The study presents significant new knowledge - because the toxic properties of mercury (or any element) are critically dependent upon its chemical form - and represents an important milestone in developing an understanding of how harmful mercury in fish might actually be. The study was carried out by SSRL staff scientists Ingrid Pickering and Graham George and postdoctoral fellow Hugh Harris using SSRL's structural molecular biology beam line 9-3. The very high flux, excellent beam stability and state-of-the-art detector technology allowed the team to measure samples of fish containing micromolar levels of mercury, much lower than had previously been possible.

191

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

192

Offshore Sulfur Comes In  

Science Journals Connector (OSTI)

Offshore Sulfur Comes In ... "The deposit is a major new source of sulfur," say Hines H. Baker, president of Humble Oil, and Langbourne M. Williams, president of Freeport Sulphur. ... Humble's deposit, known as Grand Isle (Block 18), was discovered in the course of offshore oil exploration and it ranks among the most important sulfur discoveries of recent years. ...

1956-10-01T23:59:59.000Z

193

Catalyst Additives to Enhance Mercury Oxidation and Capture  

SciTech Connect (OSTI)

Preliminary research has shown that SCR catalysts employed for nitrogen-oxide reduction can effectively oxidize mercury. This report discusses initial results from fundamental investigations into the behavior of mercury species in the presence of SCR catalysts at Southern Research Institute. The testing was performed at Southern Research's Catalyst Test Facility, a bench-scale reactor capable of simulating gas-phase reactions occurring in coal-fired utility pollution-control equipment. Three different SCR catalysts are currently being studied in this project - honeycomb-type, plate-type, and a hybrid-type catalyst. The catalysts were manufactured and supplied by Cormetech Inc., Hitachi America Ltd., and Haldor-Topsoe Inc., respectively. Parametric testing was performed to investigate the contribution of flue-gas chemistry on mercury oxidation via SCR catalysts. Methods and procedures for experimental testing continue to be developed to produce the highest quality mercury-oxidation data. Most experiments so far have focused on testing the catalysts in a simulated Powder River Basin (PRB) flue-gas environment, which contains lower sulfur and chlorine than produced by other coals. Future work to characterize flue gas simulations typically derived from low and high sulfur bituminous coal will be performed in a stepwise manner, to avoid the constant interruptions in testing that occur when leaks in the system are generated during temperature transitions. Specifically, chlorine concentration vs. mercury oxidation graph will be developed for each catalyst. The contributions of temperature and later sulfur will be investigated after this is complete. Also, last quarter's tests showed a potential linear relationship between SO3 conversion and mercury oxidation. As a result, SO3 samples will be taken more frequently to investigate each catalyst's ability to selectively oxidize mercury.

Alex J. Berry; Thomas K. Gale

2005-09-30T23:59:59.000Z

194

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

195

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

196

Mercury and Fish  

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

Mercury and Fish Mercury and Fish Name: donna Location: N/A Country: N/A Date: N/A Question: how does mercury get into fish in rivers. what is the ecological process involved which could produce toxic levels of mercury in fish and eventually get into humans? Replies: Hi Donna! Nowadays mercury or its compounds are used at a high scale in many industries as the manufacture of chemicals, paints, household itens, pesticides and fungicides. These products can contaminate humans (and mamals) by direct contact, ingestion or inhalation. Besides the air can become contaminated also, and since mercury compounds produce harmful effects in body tissues and functions, that pollution is very dangerous. Now for your question: Efluent wastes containing mercury in various forms sometimes are dropped in sea water or in rivers or lakes. There the mercury may be converted by bacteria, that are in the muddy sediments, into organic mercurial compounds particularly the highly toxic alkyl mercurials ( methyl and di-methyl mercury), which may in turn be concentrated by the fishes and other aquatic forms of life that are used as food by men. The fishes dont seem to be affected but they are able to concentrate mercury in high poisoning levels, and if human beings, mamals or birds eat these containing mercury fishes, algae, crabs or oysters they will be contaminated and poisoned.

197

Utilization of Partially Gasified Coal for Mercury Removal  

SciTech Connect (OSTI)

In this project, General Electric Energy and Environmental Research Corporation (EER) developed a novel mercury (Hg) control technology in which the sorbent for gas-phase Hg removal is produced from coal in a gasification process in-situ at a coal burning plant. The main objective of this project was to obtain technical information necessary for moving the technology from pilot-scale testing to a full-scale demonstration. A pilot-scale gasifier was used to generate sorbents from both bituminous and subbituminous coals. Once the conditions for optimizing sorbent surface area were identified, sorbents with the highest surface area were tested in a pilot-scale combustion tunnel for their effectiveness in removing Hg from coal-based flue gas. It was determined that the highest surface area sorbents generated from the gasifier process ({approx}600 m{sup 2}/g) had about 70%-85% of the reactivity of activated carbon at the same injection rate (lb/ACF), but were effective in removing 70% mercury at injection rates about 50% higher than that of commercially available activated carbon. In addition, mercury removal rates of up to 95% were demonstrated at higher sorbent injection rates. Overall, the results of the pilot-scale tests achieved the program goals, which were to achieve at least 70% Hg removal from baseline emissions levels at 25% or less of the cost of activated carbon injection.

Chris Samuelson; Peter Maly; David Moyeda

2008-09-09T23:59:59.000Z

198

DOE/NETL's Phase II Plans for Full-Scale Mercury Removal Technology Field-Testing  

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

Phase II Plans for Full-Scale Phase II Plans for Full-Scale Mercury Removal Technology Field-Testing Air Quality III September 12, 2002 Arlington, Va Scott Renninger, Project Manager for Mercury Control Technology Enviromental Projects Division Presentation Outline * Hg Program goals & objectives * Focus on Future Hg control R&D * Q&As President Bush's Clear Skies Initiative Current Mid-Term 2008-2010 2018 SO 2 11 million tons 4.5 million tons 3 million tons NOx 5 million tons 2.1 million tons 1.7 million tons Mercury 48 tons 26 tons 15 tons Annual U.S. Power Plant Emissions Mercury Control * Developing technologies ready for commercial demonstration: - By 2005, reduce emissions 50-70% - By 2010, reduce emissions by 90% - Cost 25-50% less than current estimates 2000 Year 48 Tons $2 - 5 Billion @ 90% Removal w/Activated

199

Mitigation and Remediation of Mercury Contamination at the Y-12 Plant Oak Ridge  

Broader source: Energy.gov (indexed) [DOE]

ETR-13 United States Department of Energy Office of Environmental Management (DOE-EM) External Technical Review of the Mitigation and Remediation of Mercury Contamination at the Y-12 Plant, Oak Ridge, TN Why DOE-EM Did This Review From 1953 to 1983, ~240,000 pounds of mercury (Hg) were released to the East Fork Popular Creek during the operation of the Y-12 Plant. In 1963, direct systematic releases of mercury stopped; however, mercury continues to be released into the creek from various sources of contamination in the Y-12 complex. Remediation completed up to 1992 resulted in an overall reduction of Hg loading from 150 g/day in 1983 to 15 g/day in 1992, with a current goal of 5g/day or less. The objective was to

200

MERIT Hg System Fabrication Status  

E-Print Network [OSTI]

LABORATORY U. S. DEPARTMENT OF ENERGY MC Friday Meeting 13 Jan 2006 Syringe Pump · Consists of 3 hydraulic cylinders, hydraulic pump, and manual controls · Awarded to Airline Hydraulics Corporation (AHC - Hg system cart - Magnet elevation beam · Bids currently being obtained from Oak Ridge & Princeton

McDonald, Kirk

Note: This page contains sample records for the topic "mercury hg sulfur" 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

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

202

Whole-body imaging of the distribution of mercury released from dental fillings into monkey tissues  

SciTech Connect (OSTI)

The fate of mercury (Hg) released from dental silver amalgam tooth fillings into human mouth air is uncertain. A previous report about sheep revealed uptake routes and distribution of amalgam Hg among body tissues. The present investigation demonstrates the bodily distribution of amalgam Hg in a monkey whose dentition, diet, feeding regimen, and chewing pattern closely resemble those of humans. When amalgam fillings, which normally contain 50% Hg, are made with a tracer of radioactive {sup 203}Hg and then placed into monkey teeth, the isotope appears in high concentration in various organs and tissues within 4 wk. Whole-body images of the monkey revealed that the highest levels of Hg were located in the kidney, gastrointestinal tract, and jaw. The dental profession's advocacy of silver amalgam as a stable tooth restorative material is not supported by these findings.

Hahn, L.J.; Kloiber, R.; Leininger, R.W.; Vimy, M.J.; Lorscheider, F.L. (Univ. of Calgary, Alberta (Canada))

1990-11-01T23:59:59.000Z

203

Mercury Emissions from Biomass Burning in China  

Science Journals Connector (OSTI)

Because the burned area products from remote sensors with medium resolution often miss the crop burning in fields due to its small size, we used the official statistics data at the provincial level to estimate the mercury emissions from crop residues burning in fields and biofuel combustion in homes. ... Although the amount of crop residues burnt in fields in China could not be reflected accurately in burned area products (MCD45A1) because of their small size, they could be located by MODIS fire counts data. ... Frequently burning grasslands in Africa and Australia, and agricultural waste burning globally, contribute relatively little to the Hg budget. ...

Xin Huang; Mengmeng Li; Hans R. Friedli; Yu Song; Di Chang; Lei Zhu

2011-09-27T23:59:59.000Z

204

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

205

NETL: Mercury Emissions Control Technologies - Sorbent Injection for Small  

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

Sorbent Injection for Small ESP Mercury Control in Low Sulfur Eastern Bituminous Coal Flue Gas Sorbent Injection for Small ESP Mercury Control in Low Sulfur Eastern Bituminous Coal Flue Gas URS Group and their test team will evaluate sorbent injection for mercury control on sites with low-SCA ESPs, burning low sulfur Eastern bituminous coals. Full-scale tests will be performed at Plant Yates Units 1 and 2 to evaluate sorbent injection performance across a cold-side ESP/wet FGD and a cold-side ESP with a dual NH3/SO3 flue gas conditioning system, respectively. Short-term parametric tests on Units 1 and 2 will provide data on the effect of sorbent injection rate on mercury removal and ash/FGD byproduct composition. Tests on Unit 2 will also evaluate the effect of dual-flue gas conditioning on sorbent injection performance. Results from a one-month injection test on Unit 1 will provide insight to the long-term performance and variability of this process as well as any effects on plant operations. The goals of the long-term testing are to obtain sufficient operational data on removal efficiency over time, effects on the ESP and balance of plant equipment, and on injection equipment operation to prove process viability.

206

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

207

Natural sources of mercury in arid and semiarid landscapes of western North America  

SciTech Connect (OSTI)

Mercury is enriched naturally in three global belts associated with areas in which Tertiary and Quaternary volcanism occurred. one belt, which occurs along the western margin of North America, contains concentrated and disseminated mercury occurrences in semiarid and arid biomes. Mercury enters the atmosphere from these landscapes through three processes: volatilization from enriched substrate, venting of geothermal systems, and resuspension. It is expected that the component of Hg deposited to arid landscapes through wet and dry deposition is negligible. Mercury fluxes to the atmosphere from arid and semiarid landscapes will be greater than that in more mesic environments because of the aridity and the daily amplitude in air temperatures. Resuspension may contribute significantly to the atmospheric burden of Hg due to eolian dispersal and subsequent evasion. To calculate the Hg flux from naturally enriched areas, the concentration, chemical form, and distribution of the Hg must be known. An understanding of the magnitude of natural Hg enrichment in global mercuriferous belts is important because the baseline for addressing human health and ecological risk is likely to be higher in these landscapes.

Gustin, M.S.; Taylor, G.E. Jr. [Univ. of Nevada, Reno, NV (United States). Dept. of Environmental and Resource Sciences

1994-12-31T23:59:59.000Z

208

JV Task 5 - Evaluation of Residual Oil Fly Ash As A Mercury Sorbent For Coal Combustion Flue Gas  

SciTech Connect (OSTI)

The mercury adsorption capacity of a residual oil fly ash (ROFA) sample collected form Florida Power and Light Company's Port Everglades Power Plant was evaluated using a bituminous coal combustion flue gas simulator and fixed-bed testing protocol. A size-segregated (>38 {micro}g) fraction of ROFA was ground to a fine powder and brominated to potentially enhance mercury capture. The ROFA and brominated-ROFA were ineffective in capturing or oxidizing the Hg{sup 0} present in a simulated bituminous coal combustion flue gas. In contrast, a commercially available DARCO{reg_sign} FGD initially adsorbed Hg{sup 0} for about an hour and then catalyzed Hg{sup 0} oxidation to produce Hg{sup 2+}. Apparently, the unburned carbon in ROFA needs to be more rigorously activated in order for it to effectively capture and/or oxidize Hg{sup 0}.

Robert Patton

2006-12-31T23:59:59.000Z

209

PILOT-AND FULL-SCALE DEMONSTRATION OF ADVANCED MERCURY CONTROL TECHNOLOGIES FOR LIGNITE-FIRED POWER PLANTS  

SciTech Connect (OSTI)

North Dakota lignite-fired power plants have shown a limited ability to control mercury emissions in currently installed electrostatic precipitators (ESPs), dry scrubbers, and wet scrubbers (1). This low level of control can be attributed to the high proportions of Hg{sup 0} present in the flue gas. Speciation of Hg in flue gases analyzed as part of the U.S. Environmental Protection Agency (EPA) information collection request (ICR) for Hg data showed that Hg{sup 0} ranged from 56% to 96% and oxidized mercury ranged from 4% to 44%. The Hg emitted from power plants firing North Dakota lignites ranged from 45% to 91% of the total Hg, with the emitted Hg being greater than 85% elemental. The higher levels of oxidized mercury were only found in a fluidized-bed combustion system. Typically, the form of Hg in the pulverized and cyclone-fired units was dominated by Hg{sup 0} at greater than 85%, and the average amount of Hg{sup 0} emitted from North Dakota power plants was 6.7 lb/TBtu (1, 2). The overall objective of this Energy & Environmental Research Center (EERC) project is to develop and evaluate advanced and innovative concepts for controlling Hg emissions from North Dakota lignite-fired power plants by 50%-90% at costs of one-half to three-fourths of current estimated costs. The specific objectives are focused on determining the feasibility of the following technologies: Hg oxidation for increased Hg capture in wet and dry scrubbers, incorporation of additives and technologies that enhance Hg sorbent effectiveness in ESPs and baghouses, the use of amended silicates in lignite-derived flue gases for Hg capture, and the use of Hg adsorbents within a baghouse. The scientific approach to solving the problems associated with controlling Hg emissions from lignite-fired power plants involves conducting testing of the following processes and technologies that have shown promise on a bench, pilot, or field scale: (1) activated carbon injection (ACI) upstream of an ESP combined with sorbent enhancement, (2) Hg oxidation and control using wet and dry scrubbers, (3) enhanced oxidation at a full-scale power plant using tire-derived fuel (TDF) and oxidizing catalysts, and (4) testing of Hg control technologies in the Advanced Hybrid{trademark} filter insert.

Steven A. Benson; Charlene R. Crocker; Kevin C. Galbreath; Jay R. Gunderson; Mike J. Holmes; Jason D. Laumb; Michelle R. Olderbak; John H. Pavlish; Li Yan; Ye Zhuang; Jill M. Zola

2004-02-01T23:59:59.000Z

210

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

211

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

212

DOE-NETLs Mercury R&D Program  

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

POWER-GEN POWER-GEN International 2004 -- Hg Control - Coping with Regulatory Uncertainty Orlando, FL December 1, 2004 Thomas J. Feeley, III thomas.feeley@netl.doe.gov National Energy Technology Laboratory Power-Gen, Dec. 1, 2004 History of DOE/NETL Mercury RD&D 1990 1995 2000 2005 2010 * Field testing * Plume chemistry Final Hg Regulations * Emission character- ization/ * Lab/bench- scale R&D * Monitors * Pilot-scale R&D * Byproduct characterization * Commercial demonstrations 1990 CAA Amendments Development of Regulations Development of Regulations ACS Monthly Meeting November 4 2004 DOE Mercury Control RD&D Portfolio Polishing Technology * MerCAP(tm) Sorbent Injection * Activated carbon * Amended silicates * Halogenated AC * Ca-based sorbents * Chemically treated sorbents

213

ADVANCED SULFUR CONTROL CONCEPTS  

SciTech Connect (OSTI)

Conventional sulfur removal in integrated gasification combined cycle (IGCC) power plants involves numerous steps: COS (carbonyl sulfide) hydrolysis, amine scrubbing/regeneration, Claus process, and tail-gas treatment. Advanced sulfur removal in IGCC systems involves typically the use of zinc oxide-based sorbents. The sulfides sorbent is regenerated using dilute air to produce a dilute SO{sub 2} (sulfur dioxide) tail gas. Under previous contracts the highly effective first generation Direct Sulfur Recovery Process (DSRP) for catalytic reduction of this SO{sub 2} tail gas to elemental sulfur was developed. This process is currently undergoing field-testing. In this project, advanced concepts were evaluated to reduce the number of unit operations in sulfur removal and recovery. Substantial effort was directed towards developing sorbents that could be directly regenerated to elemental sulfur in an Advanced Hot Gas Process (AHGP). Development of this process has been described in detail in Appendices A-F. RTI began the development of the Single-step Sulfur Recovery Process (SSRP) to eliminate the use of sorbents and multiple reactors in sulfur removal and recovery. This process showed promising preliminary results and thus further process development of AHGP was abandoned in favor of SSRP. The SSRP is a direct Claus process that consists of injecting SO{sub 2} directly into the quenched coal gas from a coal gasifier, and reacting the H{sub 2}S-SO{sub 2} mixture over a selective catalyst to both remove and recover sulfur in a single step. The process is conducted at gasifier pressure and 125 to 160 C. The proposed commercial embodiment of the SSRP involves a liquid phase of molten sulfur with dispersed catalyst in a slurry bubble-column reactor (SBCR).

Apostolos A. Nikolopoulos; Santosh K. Gangwal; William J. McMichael; Jeffrey W. Portzer

2003-01-01T23:59:59.000Z

214

Sulfur@Carbon Cathodes for Lithium Sulfur Batteries > Research...  

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

Electrode Channel Flow DEMS Cell Sulfur@Carbon Cathodes for Lithium Sulfur Batteries Better Ham & Cheese: Enhanced Anodes and Cathodes for Fuel Cells Epitaxial Single...

215

Sulfur-Graphene Oxide Nanocomposite Cathodes for Lithium/Sulfur...  

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

Advanced Materials Advanced Materials Find More Like This Return to Search Sulfur-Graphene Oxide Nanocomposite Cathodes for LithiumSulfur Cells Lawrence Berkeley National...

216

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

217

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

218

Investigation of increased mercury levels in the fisheries of Lower East Fork Poplar Creek (Lefpc), Oak Ridge Reservation, Tennessee  

SciTech Connect (OSTI)

The DOE Western Environmental Technology Office (WETO) is supporting remediation efforts on the U.S. Department of Energy Oak Ridge Reservation in Oak Ridge, Tennessee by performing this study. MSE Technology Applications, Inc. (MSE) has performed a series of literature reviews and bench-scale testing to further evaluate the mercury problem in the Lower East Fork Poplar Creek (LEFPC) at Oak Ridge. The primary problem is that total mercury (HgT) levels in LEFPC water decrease, while HgT levels in sunfish muscle tissue increase, with distance away from the National Security Complex (NSC), despite extensive source control efforts at the facility and within downstream riparian zones. Furthermore, dissolved methylmercury (d-MeHg) levels increase downstream from the NSC, especially during warm weather and/or high flow events. MSE performed four test series that focused on conversion of aqueous phase elemental mercury (Hg deg. A) to methyl mercury (MeHg) by algal-bacterial bio-films (periphyton) present in the stream-bed of LEFPC. Small (mg/L) quantities of un-sulphured molasses and peptone were added to some of the Hinds Creek samples to stimulate initial bacterial growth. Other Hinds Creek samples either were dosed with glutaraldehyde to preclude microbial growth, or were wrapped in aluminum foil to preclude Hg photochemical redox effects. The bench-scale testing for Phase II was completed August 2006. The final reporting and the planning for Phase III testing are in progress. (authors)

Byrne-Kelly, D.; Cornish, J.; Hart, A. [MSE Technology Applications, Inc., 200 Technology Way, Butte, MT (United States); Southworth, G. [Oak Ridge National Laboratory, Oak Ridge, TN (United States); Sims, L. [Bechtel Jacobs Company, Oak Ridge, TN (United States)

2007-07-01T23:59:59.000Z

219

Investigation of Increased Mercury Levels in the Fisheries of Lower East Fork Poplar Creek (LEFPC), Oak Ridge Reservation, Tennessee  

SciTech Connect (OSTI)

The DOE Western Environmental Technology Office (WETO) is supporting Oak Ridge's remediation efforts by performing this study. MSE Technology Applications, Inc. (MSE) has performed a series of literature reviews and bench-scale testing to further evaluate the mercury problem in the Lower East Fork Poplar Creek (LEFPC) at Oak Ridge. The primary problem is that total mercury (HgT) levels in LEFPC water decrease, while HgT levels in sunfish muscle tissue increase, with distance away from the National Security Complex (NSC), despite extensive source control efforts at the facility. Furthermore, dissolved methylmercury (d-MeHg) levels increase downstream from the NSC, especially during warm weather and/or high flow events. MSE performed four test series that focused on conversion of dissolved and colloidal forms of elemental mercury (Hg deg.A) to methyl mercury (MeHg) by algal-bacterial bio-films (periphyton) present in the stream-bed of LEFPC; MeHg production by these bio-films under anoxic versus oxic conditions was the critical measurement taken. The bench-scale testing for Phase I was completed November 2005. The final reporting and the planning for Phase II testing are in progress. (authors)

Byrne-Kelly, D.; Cornish, J.; Hart, A. [MSE Technology Applications, Inc., (United States); Southworth, G. [Oak Ridge National Laboratory (United States); Simms, L. [Bechtel Jacobs Company (United States)

2006-07-01T23:59:59.000Z

220

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

Note: This page contains sample records for the topic "mercury hg sulfur" 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

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

222

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

223

Elemental sulfur recovery process  

DOE Patents [OSTI]

An improved catalytic reduction process for the direct recovery of elemental sulfur from various SO[sub 2]-containing industrial gas streams. The catalytic process provides combined high activity and selectivity for the reduction of SO[sub 2] to elemental sulfur product with carbon monoxide or other reducing gases. The reaction of sulfur dioxide and reducing gas takes place over certain catalyst formulations based on cerium oxide. The process is a single-stage, catalytic sulfur recovery process in conjunction with regenerators, such as those used in dry, regenerative flue gas desulfurization or other processes, involving direct reduction of the SO[sub 2] in the regenerator off gas stream to elemental sulfur in the presence of a catalyst. 4 figures.

Flytzani-Stephanopoulos, M.; Zhicheng Hu.

1993-09-07T23:59:59.000Z

224

Chapter 11 - Sulfur Recovery  

Science Journals Connector (OSTI)

Abstract Sulfur is present in many raw industrial gases and in natural gas in the form of hydrogen sulfide. Sulfur removal facilities are located at the majority of oil and gas processing facilities throughout the world. The sulfur recovery unit does not make a profit for the operator but it is an essential processing step to allow the overall facility to operate, as the discharge of sulfur compounds to the atmosphere is severely restricted by environmental regulations. Concentration levels of H2S vary significantly depending upon their source. H2S produced from absorption processes, such as amine treating of natural gas or refinery gas, can contain 50–75% H2S by volume or higher. This chapter provides information about fundamentals of sulfur removal facilities in the natural gas industry.

Alireza Bahadori

2014-01-01T23:59:59.000Z

225

Measuring the pressure in ultrahigh-pressure mercury arcs  

SciTech Connect (OSTI)

Ultrahigh-pressure (UHP) mercury lamps are important as high-brightness light sources for digital projection. Hg pressures are usually above 20 MPa and difficult to measure. We have built special UHP lamps with a liquid Hg condensate in a temperature-controlled reservoir, allowing us to tune the Hg vapor pressure p between 14 and 30 MPa. As a simple measure for p, we recorded the width DELTAlambda of the 546 nm Hg line while varying p and also the lamp current I and voltage U. The data define a function p(DELTAlambda,I,U) that will deliver p to better than 3% from simple measurements of DELTAlambda, I, and U for most UHP lamps in the important 100-200 W power range. The method is applied to sample lamps, yielding pressures up to 26 MPa and demonstrating how filled Hg amount, burning position, arc gap, and lamp power affect the pressure. The effective temperature of typical UHP lamps is found to be 2400 K. We also derive an improved characteristic U(d,p,I) for the dependence of the arc voltage on arc gap, pressure, and current for electrode-stabilized Hg discharges in the UHP regime. Some aspects of the experiment are of general interest in the field of discharge lamps, such as a model for the heat balance of the Hg condensate under conductive, radiative, and evaporative cooling/heating, a short discussion of high-temperature vapor-pressure data for Hg, and an improved Hg equation of state for UHP conditions.

Hechtfischer, U.; Engelbrecht, B.; Carpaij, M.; Fischer, E.; Koerber, A. [Philips Research Laboratories, Weisshausstrasse 2, 52066 Aachen (Germany)

2009-09-01T23:59:59.000Z

226

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

227

Arctic Ocean: Is It a Sink or a Source of Atmospheric Mercury?  

Science Journals Connector (OSTI)

(4-8) Table 1 compares simulated concentrations of Hg0 and Hg2+ in air, total mercury (THg) concentrations in precipitation and snow, and snow/air Hg0 fluxes with available observed data at Alert (Canada), Ny-Ålesund (Norway), Amderma (Russia), and Barrow (USA) for 2005–2009. ... Significant AMDEs are simulated offshore near Ny-Ålesund. ... Yue, W.; Meneveau, C.; Parlange, M. B.; Zhu, W.; Kang, H. S.; Katz, J.Turbulent kinetic energy budgets in a model canopy: comparisons between LES and wind-tunnel experiments Environ. ...

Ashu P. Dastoor; Dorothy A. Durnford

2013-12-13T23:59:59.000Z

228

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

229

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

230

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

231

Controlling mercury emissions from coal-fired power plants  

SciTech Connect (OSTI)

Increasingly stringent US federal and state limits on mercury emissions form coal-fired power plants demand optimal mercury control technologies. This article summarises the successful removal of mercury emissions achieved with activated carbon injection and boiler bromide addition, technologies nearing commercial readiness, as well as several novel control concepts currently under development. It also discusses some of the issues standing in the way of confident performance and cost predictions. In testing conducted on western coal-fired units with fabric filters or TOXECON to date, ACI has generally achieved mercury removal rates > 90%. At units with ESPs, similar performance requires brominated ACI. Alternatively, units firing western coals can use boiler bromide addition to increase flue gas mercury oxidation and downstream capture in a wet scrubber, or to enhance mercury removal by ACI. At eastern bituminous fired units with ESPs, ACI is not as effective, largely due to SO{sub 3} resulting from the high sulfur content of the coal or the use of SO{sub 3} flue gas conditioning to improve ESP performance. 7 refs., 3 figs.

Chang, R. [Electric Power Research Institute, Palo Alto, CA (United States)

2009-07-15T23:59:59.000Z

232

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

233

Bacterial Sulfur Storage Globules  

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

by I. J. Pickering and G. N. George by I. J. Pickering and G. N. George Sulfur is essential for all life, but it plays a particularly central role in the metabolism of many anaerobic microorganisms. Prominent among these are the sulfide-oxidizing bacteria that oxidize sulfide (S2-) to sulfate (SO42-). Many of these organisms can store elemental sulfur (S0) in "globules" for use when food is in short supply (Fig. 1). The chemical nature of the sulfur in these globules has been an enigma since they were first described as far back as 1887 (1); all known forms (or allotropes) of elemental sulfur are solid at room temperature, but globule sulfur has been described as "liquid", and it apparently has a low density – 1.3 compared to 2.1 for the common yellow allotrope a-sulfur. Various exotic forms of sulfur have been proposed to explain these properties, including micelles (small bubble-like structures) formed from long-chain polythionates, but all of these deductions have been based upon indirect evidence (for example the density was estimated by flotation of intact cells), and many questions remained.

234

Factors Controlling the Solubility of Mercury Adsorbed on Fly Ash  

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

N:\R&D_Projects_Partial\FlyAsh&CCBs\Meetings\2005_04_WorldOfCoalAsh\AnnKim\HgSol N:\R&D_Projects_Partial\FlyAsh&CCBs\Meetings\2005_04_WorldOfCoalAsh\AnnKim\HgSol ubility_Paper.doc Factors Controlling the Solubility of Mercury Adsorbed on Fly Ash Ann G. Kim 1 and Karl Schroeder 2 1 ORISE Research Fellow, National Energy Technology Laboratory, U.S. Department of Energy, 626 Cochrans Mill Rd., Pittsburgh, PA 15236-0940 2 Research Group Leader, National Energy Technology Laboratory, U.S. Department of Energy, 626 Cochrans Mill Rd., Pittsburgh, PA 15236-0940 KEYWORDS Coal Utilization By-Products, leaching, activated carbon, pH ABSTRACT It is expected that increased controls on Hg emissions will shift the environmental burden from the flue gas to the solid coal utilization by-products (CUB), such as fly ash and flue-gas

235

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

236

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

237

Getting Started | Mercury  

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

Getting Started Getting Started Client example: open_in_t in_struct; open_out_t out_struct; /* Initialize the interface */ [...] NA_Addr_lookup(network_class, server_name, &server_addr); /* Register RPC call */ rpc_id = HG_REGISTER("open", open_in_t, open_out_t); /* Fill input parameters */ [...] in_struct.in_param0 = in_param0; /* Send RPC request */ HG_Forward(server_addr, rpc_id, &in_struct, &out_struct, &rpc_request); /* Wait for completion */ HG_Wait(rpc_request, HG_MAX_IDLE_TIME, HG_STATUS_IGNORE); /* Get output parameters */ [...] out_param0 = out_struct.out_param0; int main(int argc, void *argv[]) { /* Initialize the interface */ [...] /* Register RPC call */ HG_HANDLER_REGISTER("open", open_rpc, open_in_t, open_out_t); /* Process RPC calls */

238

Genome Sequence of Mercury-Methylating and Pleomorphic Desulfovibrio africanus strain Walvis Bay  

SciTech Connect (OSTI)

Desulfovibrio africanus strain Walvis Bay is an anaerobic sulfate-reducing bacterium capable of producing methylmercury (MeHg), a potent human neurotoxin. The mechanism of methylation by this and other organisms is unknown. We present the 4.2-Mb genome sequence to provide further insight into microbial mercury methylation and sulfate-reducing bacteria.

Brown, Steven D [ORNL; Wall, Judy D. [University of Missouri; Kucken, A M [University of Missouri, Columbia; Gilmour, C C [Smithsonian Environmental Research Center, Edgewater, MD; Podar, Mircea [ORNL; Brandt, Craig C [ORNL; Teshima, Hazuki [Los Alamos National Laboratory (LANL); Detter, J C [U.S. Department of Energy, Joint Genome Institute; Han, Cliff [Los Alamos National Laboratory (LANL); Land, Miriam L [ORNL; Lucas, Susan [U.S. Department of Energy, Joint Genome Institute; Han, James [U.S. Department of Energy, Joint Genome Institute; Pennacchio, Len [U.S. Department of Energy, Joint Genome Institute; Nolan, Matt [U.S. Department of Energy, Joint Genome Institute; Pitluck, Samual [U.S. Department of Energy, Joint Genome Institute; Woyke, Tanja [ORNL; Goodwin, Lynne A. [Los Alamos National Laboratory (LANL); Palumbo, Anthony Vito [ORNL; Elias, Dwayne A [ORNL

2011-01-01T23:59:59.000Z

239

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 Ã? Royal SwedishREPORT Pre-Colombian Mercury Pollution Associated with the Smelting of Argentiferous Ores

Wolfe, Alexander P.

240

Effect of reticuloendothelial system blockade on the biotransformation of methyl mercury in the rat  

SciTech Connect (OSTI)

It has been reported that methyl mercury (MeHg) administered to animals is biotransformed to inorganic mercury. Several studies have presented that there are two degradation process, by intestinal microflora and by animal tissues themselves. In a previous paper, the authors reported the biotransformation of MeHg in the rat was enhanced by phenylhydrazine administration, and inhibited by splenectomy or treatment with carrageenan (CAR). They suggested that spleen and liver might be the important sites for formation of inorganic mercury, and that reticuloendothelial system (RES) cells in these organs might play a major role in this biotransformation. The clearance activity of RES cells, mainly located in the liver and spleen, can be depressed by saturating those cells with CAR, colloidal carbon (CC), trypan blue (TB), colloidal iron (CFe), dextran sulfate, silica. The purpose of this study is to confirm the relationship between RES function and biotransformation of MeHg by using four representative blockers, CC, TB, CFe and CAR. The inhibited biotransformation of MeHg in RES-blocker-treated rats was evaluated by measuring the amount of total and inorganic mercury in tissues. On the other hand, RES cell activity was measured by carbon clearance tests.

Suda, Ikuo; Takahashi, Hitoshi (Kumamoto Univ. Medical School (Japan))

1990-04-01T23:59:59.000Z

Note: This page contains sample records for the topic "mercury hg sulfur" 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

NETL: News Release - We Energies Begins Operational Phase of Mercury  

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

7, 2006 7, 2006 We Energies Begins Operational Phase of Mercury Control Test in Michigan Coal-Fired Power Plant TOXECON(tm) Process Could Achieve 90 Percent Mercury Removal Washington, DC - The nation's first full-scale test of the patented TOXECON(tm) pollution control process began operations at the We Energies Presque Isle Power Plant located in Marquette, MI. The $52.9 million TOXECON(tm) project was selected by the U.S. Department of Energy in 2003 as part of the President's Clean Coal Power Initiative. Under their agreement with DOE, We Energies is designing, installing, operating and evaluating the TOXECON(tm) process as an integrated system to control emissions of mercury, particulate matter, sulfur dioxide and nitrogen oxides during the operations of its Presque Isle plant.

242

Catalyst Additives to Enhance Mercury Oxidation and Capture  

SciTech Connect (OSTI)

Preliminary research has shown that SCR catalysts employed for nitrogen-oxide reduction can effectively oxidize mercury. Three different SCR catalysts are currently being studied in this project--honeycomb-type, plate-type, and a hybrid-type catalyst. The catalysts were manufactured and supplied by Cormetech Inc., Hitachi America Ltd., and Haldor-Topsoe Inc., respectively. Parametric testing was performed to investigate the contribution of flue-gas chemistry on mercury oxidation via SCR catalysts. Future work to characterize flue gas simulations typically derived from low and high sulfur bituminous coal are being performed in a stepwise manner, to avoid the constant interruptions in testing that occur when leaks in the system are generated during temperature transitions. Specifically, chlorine concentration vs. mercury oxidation correlations will be developed for each catalyst. The contributions of temperature are also being investigated. SO2 oxidation is also being investigated for each test condition.

Thomas K. Gale

2005-12-31T23:59:59.000Z

243

Catalyst Additives to Enhance Mercury Oxidation and Capture  

SciTech Connect (OSTI)

Preliminary research has shown that SCR catalysts employed for nitrogen-oxide reduction can effectively oxidize mercury. This report discusses initial results from fundamental investigations into the behavior of mercury species in the presence of SCR catalysts at Southern Research Institute. The testing was performed at Southern Research's Catalyst Test Facility, a bench-scale reactor capable of simulating gas-phase reactions occurring in coal-fired utility pollution-control equipment. Three different SCR catalysts are currently being studied in this project--honeycomb-type, plate-type, and a hybrid-type catalyst. The catalysts were manufactured and supplied by Cormetech Inc., Hitachi America Ltd., and Haldor-Topsoe Inc., respectively. Parametric testing was performed to investigate the contribution of flue-gas chemistry on mercury oxidation via SCR catalysts. Methods and procedures for experimental testing continue to be developed to produce the highest quality mercury-oxidation data. During this past quarter, it was discovered that long periods (12 - 24 hours) are required to equilibrate the catalysts in the system. In addition, after the system has been equilibrated, operational changes to temperature, gas concentration, or flow rate shifts the equilibrium, and steady-state must be reestablished, which can require as much as twelve additional hours per condition change. In the last quarter of testing, it was shown that the inclusion of ammonia had a strong effect on the oxidation of mercury by SCR catalysts, both in the short-term (a transitional period of elemental and oxidized mercury off gassing) and the long-term (less steady-state mercury oxidation). All experiments so far have focused on testing the catalysts in a simulated Powder River Basin (PRB) flue-gas environment, which contains lower sulfur and chlorine than produced by other coals. In the next quarter, parametric testing will be expanded to include flue gases simulating power plants burning Midwestern and Eastern coals, which are higher in sulfur and chlorine. Also, the isolation of such gases as hydrogen chloride (HCl), ammonia (NH{sub 3}), and sulfur trioxide (SO{sub 3}) will be investigated. All of these efforts will be used to examine the kinetics of mercury oxidation across the SCR catalysts with respect to flue gas composition, temperature, and flow rate.

Jared W. Cannon; Thomas K. Gale

2005-06-30T23:59:59.000Z

244

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

245

Dynamic duo captures mercury  

SciTech Connect (OSTI)

There is strong evidence that the combination of wet flue gas desulphurisation (FGD) scrubbers and selective catalytic reduction (SCR) can prove a viable and formidable combination for knocking out mercury. This article analyzes the capabilities and limitations of the SCR-FGD combination for mercury compliance, including applicability to different types of coal and issues with scrubber by-products. 3 figs.

Senior, C.; Adams, B. [Reaction Engineering International (United States)

2006-02-15T23:59:59.000Z

246

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

247

Dental silver tooth fillings: A source of mercury exposure revealed by whole-body image scan and tissue analysis  

SciTech Connect (OSTI)

Mercury (Hg) vapor is released from dental silver tooth fillings into human mouth air after chewing, but its possible uptake routes and distribution among body tissues are unknown. This investigation demonstrates that when radioactive 203Hg is mixed with dental Hg/silver fillings (amalgam) and placed in teeth of adult sheep, the isotope will appear in various organs and tissues within 29 days. Evidence of Hg uptake, as determined by whole-body scanning and measurement of isotope in specific tissues, revealed three uptake sites: lung, gastrointestinal, and jaw tissue absorption. Once absorbed, high concentrations of dental amalgam Hg rapidly localize in kidneys and liver. Results are discussed in view of potential health consequences from long-term exposure to Hg from this dental material.

Hahn, L.J.; Kloiber, R.; Vimy, M.J.; Takahashi, Y.; Lorscheider, F.L. (Univ. of Calgary, Alberta (Canada))

1989-12-01T23:59:59.000Z

248

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

249

Mercury Vapor At Akutan Fumaroles Area (Kolker, Et Al., 2010) | Open Energy  

Open Energy Info (EERE)

Akutan Fumaroles Area (Kolker, Et Al., 2010) Akutan Fumaroles Area (Kolker, Et Al., 2010) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Akutan Fumaroles Area (Kolker, Et Al., 2010) Exploration Activity Details Location Akutan Fumaroles Area Exploration Technique Mercury Vapor Activity Date Usefulness useful DOE-funding Unknown Notes Arsenic (As), mercury (Hg), and carbon dioxide (CO2) all appear in anomalously high concentrations near the hot springs and at the junction of the Fumarole Valley and the HSBV. This indicates either that Hg is being lost from a reservoir due to boiling and steam loss, probably northwest of the junction, or erosion has carried these elements in sediment from the higher elevation manifestations. The presence of such volatiles in

250

In-House Research on Mercury Measurement and Control at NETL  

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

identifier identifier In-House Research on Mercury Measurement and Control at NETL identifier BACKGROUND T Over 32% of man-made emissions of Hg in U.S. are from coal-fired utilities. T Future regulation of utility emissions has been proposed by EPA. T Control of Hg emissions is complicated by low concentrations (~1 ppbv) and speciation variability. T EPA report suggests sorbent injection as a low- cost technique for mercury removal. T NETL's in-house research effort is conducted at both pilot and lab scales. identifier PILOT RESEARCH OBJECTIVES T Evaluate methods for measurement of mercury concentration and speciation. T Assess the technical performance of sorbent-based control technology by developing engineering databases. identifier identifier identifier PILOT WORK TESTING GOALS T Determine mass balances around pilot

251

NETL: Mercury Emissions Control  

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

Home > Technologies > Coal & Power Systems > Innovations for Existing Plants > Mercury Emissions Control Home > Technologies > Coal & Power Systems > Innovations for Existing Plants > Mercury Emissions Control Innovations for Existing Plants Mercury Emissions Control NETL managed the largest funded research program in the country to develop an in-depth understanding of fossil combustion-based mercury emissions. The program goal was to develop effective control options that would allow generators to comply with regulations. Research focus areas included measurement and characterization of mercury emissions, as well as the development of cost-effective control technologies for the U.S. coal-fired electric generating industry. Control Technologies Field Testing Phase I & II Phase III Novel Concepts APCD Co-benefits Emissions Characterization

252

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

253

DOE/NETL's Mercury Emissions Control Technology R&D Program  

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

Mercury Emissions Control Mercury Emissions Control Technology R&D Program LRC and Lignite Industry Meeting August 27-28, 2002 Bismarck, ND Thomas J. Feeley, III, Product Manager Innovations for Existing Plants LigniteResearch_TJF,082702 Presentation Outline * About NETL * IEP Program * Hg Background * Hg and lignite coals * Hg Control R&D LigniteResearch_TJF,082702 About NETL LigniteResearch_TJF,082702 * One of DOE's 17 national labs * Government owned / operated * Sites in: - Pennsylvania - West Virginia - Oklahoma - Alaska * More than 1,100 federal and support contractor employees National Energy Technology Laboratory LigniteResearch_TJF,082702 Electric Power Using Coal Clean Liquid Fuels Natural Gas Coal Production Environmental Control V21 Next Generation Carbon Sequestration Exploration & Production Refining &

254

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

255

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

256

Regenerative process for removal of mercury and other heavy metals from gases containing H.sub.2 and/or CO  

DOE Patents [OSTI]

A method for removal of mercury from a gaseous stream containing the mercury, hydrogen and/or CO, and hydrogen sulfide and/or carbonyl sulfide in which a dispersed Cu-containing sorbent is contacted with the gaseous stream at a temperature in the range of about 25.degree. C. to about 300.degree. C. until the sorbent is spent. The spent sorbent is contacted with a desorbing gaseous stream at a temperature equal to or higher than the temperature at which the mercury adsorption is carried out, producing a regenerated sorbent and an exhaust gas comprising released mercury. The released mercury in the exhaust gas is captured using a high-capacity sorbent, such as sulfur-impregnated activated carbon, at a temperature less than about 100.degree. C. The regenerated sorbent may then be used to capture additional mercury from the mercury-containing gaseous stream.

Jadhav, Raja A. (Naperville, IL)

2009-07-07T23:59:59.000Z

257

High pressure conversion of \\{NOx\\} and Hg and their capture as aqueous condensates in a laboratory piston-compressor simulating oxy-fuel CO2 compression  

Science Journals Connector (OSTI)

Abstract Oxy-fuel technology for CO2 capture has largely focused on combustion characteristics as a driver towards demonstration. Impurity removal studies typically centre on the how current environmental control units (FGD, SCR, activated carbon beds) operate in oxy-fuel firing. However, it is expected that some removal of \\{NOx\\} and \\{SOx\\} may occur during compression of flue gas through the lead chamber process. Some commercial systems link the capture of mercury to the formation of acid condensates (as a soluble mercury salt). Mercury in compressed flue gas represents a potential corrosion risk in the processing of CO2 from oxy-fuel combustion processes. Gas phase elemental mercury (Hg0) is difficult to remove from the flue gas and the level of cleaning required to prevent corrosion of cryogenic brazed aluminium heat exchangers is uncertain. This work has investigated the behaviour of gaseous Hg0 in pressurised oxy-fuel systems in terms of the potential capture in acidic condensates, interaction with \\{NOx\\} gases and liquid stability on de-pressurisation. The work was undertaken on an adapted laboratory scale three stage axial-piston compressor with gas and liquid sampling at pressures up to 30 bar. The main finding was that gaseous Hg0 reacts readily with NO2 formed from NO oxidation at high pressure. This reaction occurred without the presence of water, either water vapour or liquid water, contrary to speculation in the literature. Without NO2, no capture of Hg0 was observed in the compression system. Overall, the capture of mercury during compression occurred as a consequence of high pressure, longer residence time and concentration of NO2. Capture rates of 100% Hg and 75–83% \\{NOx\\} were measured from the compressor exit at 30 bar g.

Rohan Stanger; Timothy Ting; Terry Wall

2014-01-01T23:59:59.000Z

258

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

259

Microsoft Word - Updated netl Hg program white paper v.1 July2008.doc  

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

08 1 08 1 An Update on DOE/NETL's Mercury Control Technology Field Testing Program Thomas J. Feeley, III 1 and Andrew P. Jones 2 1 U.S. Department of Energy, National Energy Technology Laboratory 2 Science Applications International Corporation The U.S. Department of Energy's National Energy Technology Laboratory (NETL), under the Office of Fossil Energy's Innovations for Existing Plants (IEP) Program, manages the premier mercury (Hg) research and development (R&D) program for coal- fired power generation facilities in the world. Working collaboratively with the U.S. Environmental Protection Agency (EPA), the Electric Power Research Institute (EPRI), power plant operators, state and local agencies, and a host of research organizations

260

Sediment-water fluxes of mercury in Lavaca Bay, Texas  

SciTech Connect (OSTI)

The aqueous flux of inorganic Hg and monomethyl Hg from sediments to the water column was determined at several sites in Lavaca Bay, an estuary along the Texas Coast, historically impacted by Hg discharges. Diffusive fluxes were calculated at 15 sites using interstitial pore water gradients and compared to direct flux measurements obtained at two sites using benthic flux chambers. The diffusive flux of monomethyl mercury (MMHg), when modeled as a chloride species, varied over 3 orders /of magnitude from 0.2 to 1500 ng m{sup {minus}2} day{sup {minus}1}. Diffusive fluxes determined at a single site revealed that MMHg fluxes varied seasonally; maximal fluxes occurred in late winter to early spring. Flux chamber deployments at an impacted site revealed t hat MMHg was the Hg species entering the water column from sediments and the flux was not in steady-state; there was a strong diurnal signal with most of the MMHg flux occurring during dark periods. The flux of inorganic Hg was smaller and not as easily discernible by this method. The MMHg flux during the dark period was about 6 times greater than the estimated diffusional flux for MMHgCl, suggesting that biological and/or chemical processes near the sediment-water interface were strongly mediating the sediment-water exchange of MMHg.

Gill, G.A. [Texas A and M Univ., Galveston, TX (United States)] [Texas A and M Univ., Galveston, TX (United States); Bloom, N.S. [Frontier Geosciences Inc., Seattle, WA (United States)] [Frontier Geosciences Inc., Seattle, WA (United States); Cappellino, S. [Parametrix, Inc., Houston, TX (United States)] [Parametrix, Inc., Houston, TX (United States); Driscoll, C.T. [Syracuse Univ., NY (United States). Dept. of Civil and Environmental Engineering] [Syracuse Univ., NY (United States). Dept. of Civil and Environmental Engineering; Dobbs, C.; McShea, L. [Aluminum Co. of America, Point Comfort, TX (United States)] [Aluminum Co. of America, Point Comfort, TX (United States); Mason, R. [Univ. of Maryland, Solomons, MD (United States). Chesapeake Biological Lab.] [Univ. of Maryland, Solomons, MD (United States). Chesapeake Biological Lab.; Rudd, J.W.M. [Dept. of Fisheries and Oceans, Winnipeg, Manitoba (Canada). Freshwater Inst.] [Dept. of Fisheries and Oceans, Winnipeg, Manitoba (Canada). Freshwater Inst.

1999-03-01T23:59:59.000Z

Note: This page contains sample records for the topic "mercury hg sulfur" 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

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

262

Surface characterization and electronic structure of HgTe nanocrystalline thin films  

Science Journals Connector (OSTI)

Mercury telluride (HgTe) nanocrystalline thin films were synthesized using an electrochemical deposition technique. The surface morphology of the thin films were investigated by atomic force microscopy (AFM) as a function of the film thickness which shows that an increase in film thickness increases the surface roughness. The scaling exponents such as roughness exponent, ? and growth exponent, ? associated with the film growth, determined from surface and power spectral analysis using AFM are found to be 0.88±0.05 and 0.21±0.04 respectively. The shifting of the valence and core levels to higher binding energy as evidenced from x-ray photoelectron spectroscopy, suggest the change in electronic structure of the nano-HgTe films possibly due to the surface roughness.

S. Rath, D. Paramanik, S. N. Sarangi, S. Varma, and S. N. Sahu

2005-11-08T23:59:59.000Z

263

The structural and electronic properties of amorphous HgCdTe from first-principles calculations  

Science Journals Connector (OSTI)

Amorphous mercury cadmium telluride (a-MCT) model structures, with x being 0.125 and 0.25, are obtained from first-principles calculations. We generate initial structures by computation alchemy method. It is found that most atoms in the network of amorphous structures tend to be fourfold and form tetrahedral structures, implying that the chemical ordered continuous random network with some coordination defects is the ideal structure for a-MCT. The electronic structure is also concerned. The gap is found to be 0.30 and 0.26 eV for a-Hg0.875Cd0.125Te and a-Hg0.75Cd0.25Te model structures, independent of the composition. By comparing with the properties of crystalline MCT with the same composition, we observe a blue-shift of energy band gap. The localization of tail states and its atomic origin are also discussed.

Huxian Zhao; Xiaoshuang Chen; Jianping Lu; Haibo Shu; Wei Lu

2014-01-01T23:59:59.000Z

264

Mercury Risk Assessment  

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

ASSESSING THE MERCURY HEALTH RISKS ASSOCIATED ASSESSING THE MERCURY HEALTH RISKS ASSOCIATED WITH COAL-FIRED POWER PLANTS: IMPACTS OF LOCAL DEPOSITIONS *T.M. Sullivan 1 , F.D. Lipfert 2 , S.M. Morris 2 , and S. Renninger 3 1 Building 830, Brookhaven National Laboratory, Upton, NY 11973 2 Private Consultants 3 Department of Energy, National Energy Technology Laboratory, Morgantown, WV ABSTRACT The U.S. Environmental Protection Agency has announced plans to regulate emissions of mercury to the atmosphere from coal-fired power plants. However, there is still debate over whether the limits should be placed on a nationwide or a plant-specific basis. Before a nationwide limit is selected, it must be demonstrated that local deposition of mercury from coal-fired power plants does not impose an excessive local health risk. The principal health

265

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. Alkaline–manganese mono-cells and Li-ion accumulators, on average, contained the lowest heavy metal concentrations, while zinc–carbon 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-Willstätter-Straße 11, D-12489 Berlin (Germany); Radant, Hendrik [BAM Federal Institute for Materials Research and Testing, Department of Analytical Chemistry, Reference Materials, Richard-Willstätter-Straße 11, D-12489 Berlin (Germany); Kohlmeyer, Regina [German Federal Environment Agency (UBA), Section III 1.6 Extended Producer Responsibility, Wörlitzer Platz 1, D-06844 Dessau-Roßlau (Germany)

2014-01-15T23:59:59.000Z

266

NETL: IEP - Mercury Emissions Control: In-House R&D  

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

In-House R&D In-House R&D The scrutiny of mercury (Hg) emissions from coal-fired utilities that began with the Clean Air Act Amendments of 1990 (CAAA) resulted in a determination by the U.S. EPA that such emissions should be regulated. A number of techniques for control of mercury emissions from power plants have been evaluated at various scales. One technique that received a great deal of attention by the EPA, utilities, and technology developers was dry sorbent injection upstream of an existing particulate control device. The in-house, air toxics research effort at NETL consisted of two distinct efforts: the first was aimed at characterizing an existing pilot unit for distribution and fate of hazardous air pollutants, including mercury ; the second was examining sorbents and photochemical oxidation as means for mercury removal from flue gas at laboratory-scale.

267

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

SciTech Connect (OSTI)

The Subbituminous Energy Coalition (SEC) identified a need to re-test stack gas emissions from power plants that burn subbituminous coal relative to compliance with the EPA mercury control regulations for coal-fired plants. In addition, the SEC has also identified the specialized monitoring needs associated with mercury continuous emissions monitors (CEM). The overall objectives of the program were to develop and demonstrate solutions for the unique emission characteristics found when burning subbituminous coals. The program was executed in two phases; Phase I of the project covered mercury emission testing programs at ten subbituminous coal-fired plants. Phase II compared the performance of continuous emission monitors for mercury at subbituminous coal-fired power plants and is reported separately. Western Research Institute and a number of SEC members have partnered with Eta Energy and Air Pollution Testing to assess the Phase I objective. Results of the mercury (Hg) source sampling at ten power plants burning subbituminous coal concluded Hg emissions measurements from Powder River Basin (PBR) coal-fired units showed large variations during both ICR and SEC testing. Mercury captures across the Air Pollution Control Devices (APCDs) present much more reliable numbers (i.e., the mercury captures across the APCDs are positive numbers as one would expect compared to negative removal across the APCDs for the ICR data). Three of the seven units tested in the SEC study had previously shown negative removals in the ICR testing. The average emission rate is 6.08 lb/TBtu for seven ICR units compared to 5.18 lb/TBtu for ten units in the SEC testing. Out of the ten (10) SEC units, Nelson Dewey Unit 1, burned a subbituminous coal and petcoke blend thus lowering the total emission rate by generating less elemental mercury. The major difference between the ICR and SEC data is in the APCD performance and the mercury closure around the APCD. The average mercury removal values across the APCDs are 2.1% and 39.4% with standard deviations (STDs) of 1990 and 75%, respectively for the ICR and SEC tests. This clearly demonstrates that variability is an issue irrespective of using 'similar' fuels at the plants and the same source sampling team measuring the species. The study also concluded that elemental mercury is the main Hg specie that needs to be controlled. 2004 technologies such as activated carbon injection (ACI) may capture up to 60% with double digit lb/MMacf addition of sorbent. PRB coal-fired units have an Hg input of 7-15 lb/TBtu; hence, these units must operate at over 60% mercury efficiency in order to bring the emission level below 5.8 lb/TBtu. This was non-achievable with the best technology available as of 2004. Other key findings include: (1) Conventional particulate collectors, such as Cold-side Electro-Static Precipitators (CESPs), Hot-side Electro-Static Precipitator (HESP), and Fabric Filter (FF) remove nearly all of the particulate bound mercury; (2) CESPs perform better highlighting the flue gas temperature effect on the mercury removal. Impact of speciation with flue gas cooling is apparent; (3) SDA's do not help in enhancing adsorption of mercury vapor species; and (4) Due to consistently low chlorine values in fuels, it was not possible to analyze the impact of chlorine. In summary, it is difficult to predict the speciation at two plants that burn the same fuel. Non-fuel issues, such as flue gas cooling, impact the speciation and consequently mercury capture potential.

Alan Bland; Kumar Sellakumar; Craig Cormylo

2007-08-01T23:59:59.000Z

268

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

269

Freeport Begins Offshore Sulfur Plant  

Science Journals Connector (OSTI)

Freeport Begins Offshore Sulfur Plant ... Discovered by Humble Oil & Refining, the sulfur deposit off Grand Isle is believed by industry observers to be one of the largest discovered in recent years. ...

1958-07-07T23:59:59.000Z

270

Determination of mercury and organic mercury contents in Malaysian seafood  

Science Journals Connector (OSTI)

The contents of mercury and organic mercury in various types of seafood from various location in Malaysia were determined...Rastrelliger kanagurta), Spanish mackerel (Scomberomurus commersoni), shrimp (Peneaus sp...

S. A. Rahman; A. K. Wood; S. Sarmani…

1997-03-01T23:59:59.000Z

271

Sulfur polymer cement for macroencapsulation of mixed waste debris  

SciTech Connect (OSTI)

In FY 1997, the US DOE Mixed Waste Focus Area (MWFA) sponsored a demonstration of the macroencapsulation of mixed waste debris using sulfur polymer cement (SPC). Two mixed wastes were tested--a D006 waste comprised of sheets of cadmium and a D008/D009 waste comprised of lead pipes and joints contaminated with mercury. The demonstration was successful in rendering these wastes compliant with Land Disposal Restrictions (LDR), thereby eliminating one Mixed Waste Inventory Report (MWIR) waste stream from the national inventory.

Mattus, C.H.

1998-06-01T23:59:59.000Z

272

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

273

NETL: Mercury Emissions Inactive Mercury Projects  

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

Completed Mercury Projects Completed Mercury Projects View specific project information by clicking the state of interest on the map. Clickable U.S. Map ALABAMA Characterizing Toxic Emissions from Coal-Fired Power Plants Southern Research Institute The objective of this contract is to perform sampling and analysis of air toxic emissions at commercial coal-fired power plants in order to collect data that the EPA will use in their Congressionally mandated report on Hazardous Air Pollutants from Electric Utilities. CALIFORNIA Assessment of Toxic Emissions from a Coal-Fired Power Plant Utilizing an ESP Energy & Environmental Research Corporation – CA The overall objective of this project is to conduct comprehensive assessments of toxic emissions of two coal-fired electric utility power plants. The power plant that was assessed for toxic emissions during Phase I was American Electric Power Service Corporation's Cardinal Station Unit 1.

274

Why sequence Alkaliphilic sulfur oxidizing bacteria for sulfur pollution  

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

Alkaliphilic sulfur oxidizing Alkaliphilic sulfur oxidizing bacteria for sulfur pollution remediation? Burning sulfur-containing fuels, such as coal, oil, and natural gas, contributes significantly to global environmental problems, such as air pollution and acid rain, besides contributing to the loss of the ozone layer. One method of managing sulfur compounds released as byproducts from industrial processes is to scrub them out using chemical treatments and activated charcoal beds. A lower-cost solution relies on incorporating alkaliphic sulfur-oxidizing bacteria into biofilters to convert the volatile and toxic compounds into insoluble sulfur for easier removal. Discovered in the last decade, these bacteria have been found to thrive in habitats that span the full pH range. The bacteria could have applications

275

Prenatal mercury contamination: relation with maternal seafood consumption during pregnancy and fetal growth in the "EDEN mother-child" cohort  

E-Print Network [OSTI]

1 Prenatal mercury contamination: relation with maternal seafood consumption during pregnancy-aline.charles@inserm.fr30 Running title: Hg exposure from seafood and fetal growth inserm-00560924,version1-31Jan2011 Author Background: Maternal seafood intake is of great health interest since it constitutes an important source of n

276

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

277

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

278

Bioaccumulation of Mercury in Sharks  

E-Print Network [OSTI]

Resources: EPA General Info on Mercury - http://www.epa.gov/mercury/about.htm FDA Mercury Levels in Seafood - http://www.fda.gov/Food/GuidanceRegulation/GuidanceDocumentsRegulatoryInformation/ Seafood/ucm092041/en/index.html Monterey Bay Aquarium Sustainable Seafood Guide - http://www.montereybayaquarium.org/cr/Seafood

Miami, University of

279

Gas Mileage of 1994 Vehicles by Mercury  

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

4 Mercury Vehicles 4 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1994 Mercury Capri 4 cyl, 1.6 L, Automatic 4-spd, Regular Gasoline Compare 1994 Mercury Capri 20 City 21 Combined 24 Highway 1994 Mercury Capri 4 cyl, 1.6 L, Manual 5-spd, Regular Gasoline Compare 1994 Mercury Capri 21 City 23 Combined 26 Highway 1994 Mercury Capri 4 cyl, 1.6 L, Manual 5-spd, Regular Gasoline Compare 1994 Mercury Capri 22 City 24 Combined 28 Highway 1994 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Regular Gasoline Compare 1994 Mercury Cougar 17 City 19 Combined 24 Highway 1994 Mercury Cougar 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 1994 Mercury Cougar 16 City 18 Combined 23 Highway 1994 Mercury Grand Marquis 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 1994 Mercury Grand Marquis 16

280

Gas Mileage of 1985 Vehicles by Mercury  

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

5 Mercury Vehicles 5 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1985 Mercury Capri 4 cyl, 2.3 L, Automatic 3-spd, Regular Gasoline Compare 1985 Mercury Capri 19 City 20 Combined 23 Highway 1985 Mercury Capri 4 cyl, 2.3 L, Manual 4-spd, Regular Gasoline Compare 1985 Mercury Capri 21 City 23 Combined 27 Highway 1985 Mercury Capri 6 cyl, 3.8 L, Automatic 3-spd, Regular Gasoline Compare 1985 Mercury Capri 17 City 18 Combined 20 Highway 1985 Mercury Capri 8 cyl, 5.0 L, Manual 5-spd, Regular Gasoline Compare 1985 Mercury Capri 15 City 17 Combined 22 Highway 1985 Mercury Capri 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1985 Mercury Capri 15 City 17 Combined 22 Highway 1985 Mercury Capri 4 cyl, 2.3 L, Automatic 3-spd, Regular Gasoline Compare 1985 Mercury Capri 18 City

Note: This page contains sample records for the topic "mercury hg sulfur" 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

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

282

NETL: Mercury Emissions Control Technologies - Oxidation of Mercury Across  

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

Oxidation of Mercury Across SCR Catalysts in Coal-Fired Power Plants Burning Low Rank Fuels Oxidation of Mercury Across SCR Catalysts in Coal-Fired Power Plants Burning Low Rank Fuels The objective of the proposed research is to assess the potential for the oxidation of mercury in flue gas across SCR catalysts in a coal fired power plant burning low rank fuels using a slipstream reactor containing multiple commercial catalysts in parallel. Results from the project will contribute to a greater understanding of mercury behavior across SCR catalysts. Additional tasks include: review existing pilot and field data on mercury oxidation across SCR catalysts and propose a mechanism for mercury oxidation and create a simple computer model for mercury oxidation based on the hypothetical mechanism. Related Papers and Publications: Final Report - December 31, 2004 [PDF-532KB]

283

XAFS Investigation of Mercury Sorption on Carbon-based and Other Sorbent Materials  

Science Journals Connector (OSTI)

The sorption of mercury from simulated coal combustion flue gases on coal-derived chars, activated carbons, and zeolites has been examined using mercury LIII XAFS spectroscopy. The energy difference between the two inflection points (IPD) in the mercury XANES spectra has been shown to be a sensitive indicator of the local structure around the mercury adsorbed on the sorbent. The value of the IPD appears to reflect the form of mercury added to the flue gas and to be sensitive to acidic gaseous species such as HCl and H2SO4 that may be present in the flue gas, whether from addition to the flue gas or from the sulfur and chlorine in the coal. The data suggest that well-defined mercury species are not formed on carbon-based sorbents, but rather the structure and chemistry of the sorbed mercury species reflect the different anionic species present in the flue gas, as well as any activating element on the sorbent itself.

Frank E. Huggins; Nora Yap; Gerald P. Huffman

1999-01-01T23:59:59.000Z

284

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

285

Assessment of mercury health risks to adults from coal combustion  

SciTech Connect (OSTI)

The U.S. Environmental Protection Agency (EPA) is preparing, for the U.S. Congress, a report evaluating the need to regulate mercury (Hg) emissions from electric utilities. This study, to be completed in 1995, will have important health and economic implications. In support of these efforts, the U.S. Department of Energy, Office of Fossil Energy, sponsored a risk assessment project at Brookhaven National Laboratory (BNL) to evaluate methylmercury (MeHg) hazards independently. In the BNL study, health risks to adults resulting from Hg emissions from a hypothetical 1000 MW{sub e} coal-fired power plant were estimated using probabilistic risk assessment techniques. The approach draws on the extant knowledge in each of the important steps in the calculation chain from emissions to health effects. Estimated results at key points in the chain were compared with actual measurements to help validate the modeled estimates. Two cases were considered: the baseline case (no local impacts), and the impact case (maximum local power-plant impact). The BNL 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. Many implicit and explicit sources of uncertainty exist in this analysis. Those that appear to be most in need of improvement include data on doses and responses for potentially sensitive subpopulations (e.g., fetal exposures). Rather than considering hypothetical situations, it would also be preferable to assess the risks associated with actual coal-fired power plants and the nearby sensitive water bodies and susceptible subpopulations. Finally, annual total Hg emissions from coal burning and from other anthropogenic sources are still uncertain; this makes it difficult to estimate the effects of U.S. coal burning on global Hg concentration levels, especially over the long term.

Lipfert, F.W.; Moskowitz, P.D.; Fthenakis, V.M.; DePhillips, M.P.; Viren, J.; Saroff, L.

1994-05-01T23:59:59.000Z

286

Adsorption and Oxidation of Elemental Mercury over Ce-MnOx/Ti-PILCs  

Science Journals Connector (OSTI)

A series of innovative Ce–Mn/Ti-pillared-clay (Ce–Mn/Ti-PILC) catalysts combining the advantages of PILCs and Ce–Mn were investigated for elemental mercury (Hg0) capture at 100–350 °C in the absence of HCl in the flue gas. ... The catalyst characterization indicated that the 6%Ce-6%MnOx/Ti-PILC catalyst possessed a large specific surface area and high dispersion of Ce and Mn on the surface. ... The experimental results indicated that the 6%Ce-6%MnOx/Ti-PILC catalyst exhibited high Hg0 capture (>90%) at 100–350 °C. ...

Chuan He; Boxiong Shen; Jianhong Chen; Ji Cai

2014-06-23T23:59:59.000Z

287

Mercury Vapor | Open Energy Information  

Open Energy Info (EERE)

Mercury Vapor Mercury Vapor Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Technique: Mercury Vapor Details Activities (23) Areas (23) Regions (0) NEPA(0) Exploration Technique Information Exploration Group: Lab Analysis Techniques Exploration Sub Group: Fluid Lab Analysis Parent Exploration Technique: Fluid Lab Analysis Information Provided by Technique Lithology: Stratigraphic/Structural: Anomalously high concentrations can indicate high permeability or conduit for fluid flow Hydrological: Field wide soil sampling can generate a geometrical approximation of fluid circulation Thermal: High concentration in soils can be indicative of active hydrothermal activity Dictionary.png Mercury Vapor: Mercury is discharged as a highly volatile vapor during hydrothermal

288

Ultraviolet Light Initiated Oxidation of Elemental Hg  

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

The PCO Process for Removal of Mercury from Flue Gas The PCO Process for Removal of Mercury from Flue Gas Christopher R. McLarnon, Ph.D. Powerspan Corp., P.O. Box 219, 54 Old Bay Road, New Durham, NH 03855 Evan J. Granite* and Henry W. Pennline National Energy Technology Laboratory, United States Department of Energy, P.O. Box 10940, MS 58-106, Pittsburgh, PA 15236-0940 *Corresponding author. Tel.: +1412-386-4607; fax: +1412-386-6004 E-mail address: evan.granite@netl.doe.gov Abstract A promising technology has been developed to capture and remove elemental mercury species from coal-fired power plants. Powerspan Corp. has licensed the technology and initiated a bench and pilot test program to develop the Photochemical Oxidation, or PCO(tm), process for

289

Levels of mercury in scalp hair of fishermen and their families from Camara de Lobos-Madeira (Portugal): A preliminary study  

SciTech Connect (OSTI)

Mercury is probably one of the most investigated natural and anthropogenic contaminants, especially in aquatic environments. Among the inorganic forms, elemental mercury (HgO) presents a marked tendency to reach the air as vapor, and in terrestrial systems to bioaccumulate in plant biomass, whereas other inorganic compounds (e.g., mercury sulphide) are characterized by low mobility and bioavailability. These last compounds once in water (and especially at the water-sediment interface) can undergo a process of methylation. Methylmercury (MeHg) is readily bioaccumulated by aquatic organisms and leads to a phenomenon of enrichment from lower to higher trophic level. The extensive literature on MeHg and human health shows that the consumption of fish and/or shellfish is the main source of exposure, the contribution from air and water being negligible and mainly related to inorganic forms. A human population consuming large amounts of seafood with high MeHg levels can be considered at risk when consumption exceeds a certain amount. This level has been set by the WHO and other agencies, at 300 {mu}g/week of total mercury (totHg) of which there should be no more than 200 {mu}g as MeHg. The nervous system is the principal target of the effects of MeHg in humans. The most common functions affected are the sensory, visual and auditory functions, together with those of the cerebellum, which is concerned with coordination. As far as prenatal exposure is concerned, the developing central nervous system of humans and animals has been found to be more sensitive to damage from MeHg than the adult nervous system. This preliminary study obtains and examines information about eating habits and general health of a group of fisherman and their families living in a fishing village, at high risk because of the high frequency of seafood in their normal diet. 17 refs., 1 fig., 1 tab.

Gaggi, C.; Zino, F.; Duccini, M.; Renzoni, A. [Universita di Siena (Italy)] [Universita di Siena (Italy)

1996-12-31T23:59:59.000Z

290

Gas Mileage of 1986 Vehicles by Mercury  

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

6 Mercury Vehicles 6 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1986 Mercury Capri 4 cyl, 2.3 L, Automatic 3-spd, Regular Gasoline Compare 1986 Mercury Capri 18 City 20 Combined 23 Highway 1986 Mercury Capri 4 cyl, 2.3 L, Manual 4-spd, Regular Gasoline Compare 1986 Mercury Capri 21 City 23 Combined 26 Highway 1986 Mercury Capri 6 cyl, 3.8 L, Automatic 3-spd, Regular Gasoline Compare 1986 Mercury Capri 17 City 19 Combined 22 Highway 1986 Mercury Capri 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1986 Mercury Capri 15 City 18 Combined 24 Highway 1986 Mercury Capri 8 cyl, 5.0 L, Manual 5-spd, Regular Gasoline Compare 1986 Mercury Capri View MPG Estimates Shared By Vehicle Owners 15 City 18 Combined 23 Highway 1986 Mercury Cougar 4 cyl, 2.3 L, Automatic 3-spd, Regular Gasoline

291

Gas Mileage of 1991 Vehicles by Mercury  

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

1 Mercury Vehicles 1 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1991 Mercury Capri 4 cyl, 1.6 L, Automatic 4-spd, Regular Gasoline Compare 1991 Mercury Capri 21 City 22 Combined 24 Highway 1991 Mercury Capri 4 cyl, 1.6 L, Manual 5-spd, Regular Gasoline Compare 1991 Mercury Capri View MPG Estimates Shared By Vehicle Owners 21 City 23 Combined 26 Highway 1991 Mercury Capri 4 cyl, 1.6 L, Manual 5-spd, Regular Gasoline Compare 1991 Mercury Capri 22 City 24 Combined 28 Highway 1991 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Regular Gasoline Compare 1991 Mercury Cougar 17 City 20 Combined 24 Highway 1991 Mercury Cougar 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1991 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 16 City 18 Combined 22 Highway 1991 Mercury Grand Marquis 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline

292

Demonstration of Mixed Waste Debris Macroencapsulation Using Sulfur Polymer Cement  

SciTech Connect (OSTI)

This report covers work performed during FY 1997 as part of the Evaluation of Sulfur Polymer Cement Fast-Track System Project. The project is in support of the ``Mercury Working Group/Mercury Treatment Demonstrations - Oak Ridge`` and is described in technical task plan (TTP) OR-16MW-61. Macroencapsulation is the treatment technology required for debris by the U.S. Environmental Protection Agency Land Disposal Restrictions (LDR) under the Resource Conservation and Recovery Act. Based upon the results of previous work performed at Oak Ridge, the concept of using sulfur polymer cement (SPC) for this purpose was submitted to the Mixed Waste Focus Area (MWFA). Because of the promising properties of the material, the MWFA accepted this Quick Win project, which was to demonstrate the feasibility of macroencapsulation of actual mixed waste debris stored on the Oak Ridge Reservation. The waste acceptance criteria from Envirocare, Utah, were chosen as a standard for the determination of the final waste form produced. During this demonstration, it was shown that SPC was a good candidate for macroencapsulation of mixed waste debris, especially when the debris pieces were dry. The matrix was found to be quite easy to use and, once the optimum operating conditions were identified, very straightforward to replicate for batch treatment. The demonstration was able to render LDR compliant more than 400 kg of mixed wastes stored at the Oak Ridge National Laboratory.

Mattus, C.H.

1998-07-01T23:59:59.000Z

293

It's Elemental - The Element Sulfur  

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

Phosphorus Phosphorus Previous Element (Phosphorus) The Periodic Table of Elements Next Element (Chlorine) Chlorine The Element Sulfur [Click for Isotope Data] 16 S Sulfur 32.065 Atomic Number: 16 Atomic Weight: 32.065 Melting Point: 388.36 K (115.21°C or 239.38°F) Boiling Point: 717.75 K (444.60°C or 832.28°F) Density: 2.067 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Non-metal Period Number: 3 Group Number: 16 Group Name: Chalcogen What's in a name? From the Sanskrit word sulvere and the Latin word sulphurium. Say what? Sulfur is pronounced as SUL-fer. History and Uses: Sulfur, the tenth most abundant element in the universe, has been known since ancient times. Sometime around 1777, Antoine Lavoisier convinced the rest of the scientific community that sulfur was an element. Sulfur is a

294

Why sequence purple sulfur bacteria?  

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

purple sulfur bacteria? purple sulfur bacteria? The process by which plants and some bacteria can convert light energy to sugar, or photosynthesis, is crucial to global food webs, and complicated. Very little is known about the photosynthetic bacteria in the purple sulfur bacteria group, which may represent one of the most primitive photosynthetic organisms and are capable of carbon fixation and sequestration in both light and dark conditions with the help of sulfur compounds. Purple sulfur bacteria are autotrophic and can synthesize organic compounds from inorganic sources. Researchers hope to learn more by sequencing nine type strains of purple sulfur bacteria that are found in freshwater, brackish and marine systems. The information would lead to a better understanding of the process of photosynthesis as well as the global

295

Mercury Vapor At Long Valley Caldera Area (Klusman & Landress, 1979) | Open  

Open Energy Info (EERE)

Long Valley Caldera Area (Klusman & Landress, 1979) Long Valley Caldera Area (Klusman & Landress, 1979) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Long Valley Caldera Area (Klusman & Landress, 1979) Exploration Activity Details Location Long Valley Caldera Area Exploration Technique Mercury Vapor Activity Date Usefulness useful DOE-funding Unknown Notes This study involved the field collection and laboratory analysis of Al-horizon soil samples in the vicinity of a known geothermal source at Long Valley, California. The samples were analyzed for several constituents known to have influence on Hg retention by soils, including pH, hydrous Fe and Mn, and organic carbon, as well as Hg. The data compiled for these secondary parameters and the field-determined parameters of geology, soil

296

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 Laboratory’s 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

297

DOE-NETL's Mercury R&D Program  

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

Laboratory's Laboratory's Water-Energy R&D Activities LERDWG Meeting Washington, DC February 27, 2003 Thomas J. Feeley, IIII National Energy Technology Laboratory TJF_LERDWG_022703 Presentation Outline * Watershed Science & Technology * Oil & Gas/CBM Produced Waters * Carbon sequestration * Electric Utilities & Water TJF_LERDWG_022703 NETL's Watershed Science & Technology Research Activities * Remote sensing capabilities: - Thermal infrared - Very-low frequency - Magnetometry - Terrain conductivity * Used to survey/map surface and sub-surface ground water sources and point/non-point discharges * Active, passive, and semi-passive treatment technologies NETL Airborne Remote Sensing Platform Conductivity "Stack" of Sulfur Bank Mercury Mine TJF_LERDWG_022703 Coalbed

298

Classification of carbon in Canadian fly ashes and their implications in the capture of mercury  

Science Journals Connector (OSTI)

Fly ashes produced from Canadian power plants using pulverized coal and fluidized bed combustors were examined for their carbon content to determine their ability to capture mercury. The feed coal used in these power plants were lignite, subbituminous, high and medium volatile bituminous, their blends, and also blends of coal with petroleum coke (Petcoke). The carbon and mercury content of the coals and fly ashes were determined using the ASTM standard method and by the cold vapour atomic absorption spectrometry method. The carbon content of the fly ash was concentrated by strong acid digestion using \\{HCl\\} and HF. The quantitative and qualitative analyses of the carbon concentrate were made by using a reflected light microscope. The results show that the carbon content of fly ash appears to be partially related to depositional environment during coalification and to the rank of the coal. The Hg captured by the fly ash depends on the rank and blend of the feed coals and the type of carbon in the fly ash. The isotropic vitrinitic char is mostly responsible for the capture of most Hg in fly ash. The inadvertent increase in carbon content due to the blending of coal with petroleum coke did not increase the amount Hg captured by the fly ash. The fly ash collected by the hot side electrostatic precipitator has a low Hg content and no relation between the Hg and carbon content of the ash was observed. These results indicate that the quantity of carbon in the fly ash alone does not determine the amount Hg captured. The types of carbon present (isotropic and anisotropic vitrinitic, isotropic inertinitic and anisotropic Petcoke), the halogen content, the types of fly ash control devices, and the temperatures of the fly ash control devices all play major roles in the capture of Hg.

Fariborz Goodarzi; James C. Hower

2008-01-01T23:59:59.000Z

299

Environmental Sampling FY01 Annual Report - Understanding the Movement of Mercury in the Environmental Surrounding the INEEL  

SciTech Connect (OSTI)

Environmental fate and transport of the toxic air pollutant mercury (Hg) is currently a high-priority regional concern for the INEEL, and national and global concern for the U.S. Environmental Protection Agency (EPA). At the INEEL’s Idaho Nuclear Technology and Engineering Center (INTEC), significant quantities (est. 40 kg/year) of Hg may have been released over 37 years of Environmental Management’s (EM) High-Level Waste (HLW) treatment operations. The EPA is very concerned about the continued global buildup of Hg in the atmosphere and aquatic ecosystems, and has recently invested heavily in Hg research to better understand its complex environmental cycling.1,2 The Environmental Sampling work began in FY99 as a joint INEEL/U.S. Geological Survey (USGS) field research effort to (a) better understand the fate and potential impacts of Hg emissions from the INEEL’s HLW treatment operations (operational component) and (b) contribute at a national level to the scientific understanding of local, regional, and global Hg fate and transport (research component). The USGS contributed snow sampling support in the field (Water Resources Division, Salt Lake City) and laboratory analysis of all samples (Wisconsin District Mercury Research Laboratory).

Abbott, Michael Lehman

2001-09-01T23:59:59.000Z

300

Microbial transformations of sulfur compounds  

Science Journals Connector (OSTI)

Oct 13, 1978 ... tains a large part of the chemical energy transferred ... ical energy is partly preserved in the bio- mass of .... ethanol to remove elemental sulfur.

2000-01-10T23:59:59.000Z

Note: This page contains sample records for the topic "mercury hg sulfur" 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

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

302

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

303

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

304

Gas Mileage of 2002 Vehicles by Mercury  

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

2 Mercury Vehicles 2 Mercury Vehicles EPA MPG MODEL City Comb Hwy 2002 Mercury Cougar 4 cyl, 2.0 L, Manual 5-spd, Regular Gasoline Compare 2002 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 21 City 24 Combined 31 Highway 2002 Mercury Cougar 6 cyl, 2.5 L, Automatic 4-spd, Regular Gasoline Compare 2002 Mercury Cougar 18 City 21 Combined 26 Highway 2002 Mercury Cougar 6 cyl, 2.5 L, Manual 5-spd, Regular Gasoline Compare 2002 Mercury Cougar 18 City 21 Combined 27 Highway 2002 Mercury Grand Marquis 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 2002 Mercury Grand Marquis View MPG Estimates Shared By Vehicle Owners 15 City 18 Combined 23 Highway 2002 Mercury Mountaineer 2WD 6 cyl, 4.0 L, Automatic 5-spd, Regular Gasoline Compare 2002 Mercury Mountaineer 2WD 14 City

305

Gas Mileage of 1989 Vehicles by Mercury  

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

9 Mercury Vehicles 9 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1989 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Regular Gasoline Compare 1989 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 17 City 20 Combined 25 Highway 1989 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Premium Gasoline Compare 1989 Mercury Cougar 15 City 17 Combined 21 Highway 1989 Mercury Cougar 6 cyl, 3.8 L, Manual 5-spd, Premium Gasoline Compare 1989 Mercury Cougar 15 City 18 Combined 22 Highway 1989 Mercury Grand Marquis 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1989 Mercury Grand Marquis View MPG Estimates Shared By Vehicle Owners 15 City 18 Combined 22 Highway 1989 Mercury Grand Marquis Wagon 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1989 Mercury Grand Marquis Wagon 15

306

Gas Mileage of 1993 Vehicles by Mercury  

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

3 Mercury Vehicles 3 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1993 Mercury Capri 4 cyl, 1.6 L, Automatic 4-spd, Regular Gasoline Compare 1993 Mercury Capri 20 City 21 Combined 24 Highway 1993 Mercury Capri 4 cyl, 1.6 L, Manual 5-spd, Regular Gasoline Compare 1993 Mercury Capri View MPG Estimates Shared By Vehicle Owners 21 City 23 Combined 26 Highway 1993 Mercury Capri 4 cyl, 1.6 L, Manual 5-spd, Regular Gasoline Compare 1993 Mercury Capri View MPG Estimates Shared By Vehicle Owners 22 City 24 Combined 28 Highway 1993 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Regular Gasoline Compare 1993 Mercury Cougar 17 City 19 Combined 24 Highway 1993 Mercury Cougar 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1993 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 15

307

Gas Mileage of 2008 Vehicles by Mercury  

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

8 Mercury Vehicles 8 Mercury Vehicles EPA MPG MODEL City Comb Hwy 2008 Mercury Grand Marquis FFV 8 cyl, 4.6 L, Automatic 4-spd, Regular Gas or E85 Compare 2008 Mercury Grand Marquis FFV Gas 15 City 18 Combined 23 Highway E85 11 City 13 Combined 16 Highway 2008 Mercury Mariner 4WD 4 cyl, 2.3 L, Automatic 4-spd, Regular Gasoline Compare 2008 Mercury Mariner 4WD 19 City 21 Combined 24 Highway 2008 Mercury Mariner 4WD 6 cyl, 3.0 L, Automatic 4-spd, Regular Gasoline Compare 2008 Mercury Mariner 4WD View MPG Estimates Shared By Vehicle Owners 17 City 19 Combined 22 Highway 2008 Mercury Mariner FWD 4 cyl, 2.3 L, Automatic 4-spd, Regular Gasoline Compare 2008 Mercury Mariner FWD 20 City 22 Combined 26 Highway 2008 Mercury Mariner FWD 6 cyl, 3.0 L, Automatic 4-spd, Regular Gasoline Compare 2008 Mercury Mariner FWD

308

Gas Mileage of 1987 Vehicles by Mercury  

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

7 Mercury Vehicles 7 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1987 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Regular Gasoline Compare 1987 Mercury Cougar 17 City 19 Combined 24 Highway 1987 Mercury Cougar 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1987 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 16 City 19 Combined 24 Highway 1987 Mercury Grand Marquis 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1987 Mercury Grand Marquis View MPG Estimates Shared By Vehicle Owners 16 City 19 Combined 24 Highway 1987 Mercury Grand Marquis Wagon 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1987 Mercury Grand Marquis Wagon 16 City 19 Combined 24 Highway 1987 Mercury Lynx 4 cyl, 1.9 L, Automatic 3-spd, Regular Gasoline Compare 1987 Mercury Lynx 23

309

Gas Mileage of 1990 Vehicles by Mercury  

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

90 Mercury Vehicles 90 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1990 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Premium Gasoline Compare 1990 Mercury Cougar 15 City 18 Combined 21 Highway 1990 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Regular Gasoline Compare 1990 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 17 City 20 Combined 24 Highway 1990 Mercury Cougar 6 cyl, 3.8 L, Manual 5-spd, Premium Gasoline Compare 1990 Mercury Cougar 15 City 18 Combined 22 Highway 1990 Mercury Grand Marquis 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1990 Mercury Grand Marquis View MPG Estimates Shared By Vehicle Owners 15 City 18 Combined 22 Highway 1990 Mercury Grand Marquis Wagon 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1990 Mercury Grand Marquis Wagon 15

310

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

311

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

312

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

313

ASSESING THE IMPACTS OF LOCAL DEPOSITION OF MERCURY ASSOCIATED WITH COAL-FIRED POWER PLANTS.  

SciTech Connect (OSTI)

Mercury emissions from coal fired plants will be limited by regulations enforced by the Environmental Protection Agency. However, there is still debate over whether the limits should be on a plant specific basis or a nationwide basis. The nationwide basis allows a Cap and Trade program similar to that for other air pollutants. Therefore, a major issue is the magnitude and extent of local deposition. Computer modeling suggests that increased local deposition will occur on a local (2 to 10 Km) to regional scale (20 to 50 Km) with the increase being a small percentage of background deposition on the regional scale. The amount of deposition depends upon many factors including emission rate, chemical form of mercury emitted (with reactive gaseous mercury depositing more readily than elemental mercury), other emission characteristics (stack height, exhaust temperature, etc), and meteorological conditions. Modeling suggests that wet deposition will lead to the highest deposition rates and that these will occur locally. Dry deposition is also predicted to deposit approximately the same amount of mass as wet deposition, but over a much greater area. Therefore, dry deposition rates will contribute a fraction of total deposition on the regional scale. The models have a number of assumptions pertaining to deposition parameters and there is uncertainty in the predicted deposition rates. A key assumption in the models is that the mixture of reactive gaseous mercury (RGM) to elemental mercury Hg(0) is constant in the exhaust plume. Recent work suggests that RGM converts to Hg(0) quickly. Deposition measurements around coal-fired power plants would help reduce the uncertainties in the models. A few studies have been performed to examine the deposition of mercury around point sources. Measurement of soil mercury downwind from chlor-alkali plants has shown increased deposition within a few Km. Studies of soils, sediments, and wet deposition around coal plants typically find some evidence of enhanced deposition; however, the statistical significance of the results is generally weak. A review of these studies is found in Lipfert. This study combines modeling of mercury deposition patterns with soil mercury measurements. The model used emissions data, meteorological conditions, and plant data to define sample locations likely to exhibit deposition in excess of background, that can be attributed to the power plant. Data were collected at the specified locations in November, 2003.

SULLIVAN, T.; BOWERMAN, B.; ADAMS, J.; OGEKA, C.; LIPFERT, F.; RENNINGER, S.

2004-03-28T23:59:59.000Z

314

Mercury emissions from municipal solid waste combustors. An assessment of the current situation in the United States and forecast of future emissions  

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.

none,

1993-05-01T23:59:59.000Z

315

Hg System Status V.B. Graves  

E-Print Network [OSTI]

· Hydraulic power unit (HPU) and syringe cylinders delivered to ORNL July 21 - Hg cylinder discharge piping cart until secondary containment received #12;3MC Friday Meeting4 Aug 2006 OAK RIDGE NATIONAL LABORATORY U. S. DEPARTMENT OF ENERGY HPU Setup · Hydraulic fluid fill and drain process developed using

McDonald, Kirk

316

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

317

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

318

Category:Mercury Vapor | Open Energy Information  

Open Energy Info (EERE)

search GEOTHERMAL ENERGYGeothermal Home Geothermalpower.jpg Looking for the Mercury Vapor page? For detailed information on Mercury Vapor as exploration techniques,...

319

Permitted Mercury Storage Facility Notifications | Department...  

Broader source: Energy.gov (indexed) [DOE]

Services Waste Management Waste Disposition Long-Term Management and Storage of Elemental Mercury is in the Planning Stages Permitted Mercury Storage Facility...

320

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

Note: This page contains sample records for the topic "mercury hg sulfur" 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.


321

Oxidation of mercury across selective catalytic reduction catalysts in coal-fired power plants  

SciTech Connect (OSTI)

A kinetic model for predicting the amount of mercury (Hg) oxidation across selective catalytic reduction (SCR) systems in coal-fired power plants was developed and tested. The model incorporated the effects of diffusion within the porous SCR catalyst and the competition between ammonia and Hg for active sites on the catalyst. Laboratory data on Hg oxidation in simulated flue gas and slipstream data on Hg oxidation in flue gas from power plants were modeled. The model provided good fits to the data for eight different catalysts, both plate and monolith, across a temperature range of 280-420{sup o}C, with space velocities varying from 1900 to 5000 hr{sup -1}. Space velocity, temperature, hydrochloric acid content of the flue gas, ratio of ammonia to nitric oxide, and catalyst design all affected Hg oxidation across the SCR catalyst. The model can be used to predict the impact of coal properties, catalyst design, and operating conditions on Hg oxidation across SCRs. 20 refs., 9 figs., 2 tabs.

Constance L. Senior [Reaction Engineering International, Salt Lake City, UT (United States)

2006-01-15T23:59:59.000Z

322

Magnetoacoustic Effect in Mercury  

Science Journals Connector (OSTI)

Geometric resonances in the ultrasonic attenuations have been observed in high-purity mercury single crystals with longitudinal sound waves propagated along five crystallographic directions at frequencies up to 165 MHz. Of the five, only data for the (11¯0), (110), and (112¯) directions are reported. The dominant resonance branches have been assigned to calipers of the second-band electron-lens surface, with three major symmetry calipers being obtained. The remainder of the resonance branches have been assigned to orbits on the first-band hole surface. Various breakthrough dimensions of the hole surface were determined from these orbits. The pseudopotential coefficients corresponding to the planes bounding the first Brillouin zone in mercury have been estimated by comparing the geometric resonance data with the results of a fourpseudowave calculation neglecting spin-orbit coupling.

Tommy E. Bogle; Julian B. Coon; Claude G. Grenier

1969-01-15T23:59:59.000Z

323

Effect of the shutdown of a large coal-fired power plant on ambient mercury  

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

Effect of the shutdown of a large coal-fired power plant on ambient mercury Effect of the shutdown of a large coal-fired power plant on ambient mercury species Title Effect of the shutdown of a large coal-fired power plant on ambient mercury species Publication Type Journal Article LBNL Report Number LBNL-6097E Year of Publication 2013 Authors Wang, Yungang, Jiaoyan Huang, Philip K. Hopke, Oliver V. Rattigan, David C. Chalupa, Mark J. Utell, and Thomas M. Holsen Journal Chemosphere Volume 92 Issue 4 Pagination 360-367 Date Published 07/2013 Abstract In the spring of 2008, a 260MWe coal-fired power plant (CFPP) located in Rochester, New York was closed over a 4 month period. Using a 2-years data record, the impacts of the shutdown of the CFPP on nearby ambient concentrations of three Hg species were quantified. The arithmetic average ambient concentrations of gaseous elemental mercury (GEM), gaseous oxidized mercury (GOM), and particulate mercury (PBM) during December 2007-November 2009 were 1.6ng/m3, 5.1pg/m3, and 8.9pg/m3, respectively. The median concentrations of GEM, GOM, and PBM significantly decreased by 12%, 73%, and 50% after the CFPP closed (Mann-Whitney test, p<0.001). Positive Matrix Factorization (EPA PMF v4.1) identified six factors including O3-rich, traffic, gas phase oxidation, wood combustion, nucleation, and CFPP. When the CFPP was closed, median concentrations of GEM, GOM, and PBM apportioned to the CFPP factor significantly decreased by 25%, 74%, and 67%, respectively, compared to those measured when the CFPP was still in operation (Mann-Whitney test, p<0.001). Conditional probability function (CPF) analysis showed the greatest reduction in all three Hg species was associated with northwesterly winds pointing toward the CFPP. These changes were clearly attributable to the closure of the CFPP.

324

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

325

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

326

Gas Mileage of 2000 Vehicles by Mercury  

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

2000 Mercury Vehicles 2000 Mercury Vehicles EPA MPG MODEL City Comb Hwy 2000 Mercury Cougar 4 cyl, 2.0 L, Manual 5-spd, Regular Gasoline Compare 2000 Mercury Cougar 21 City 25 Combined 31 Highway 2000 Mercury Cougar 6 cyl, 2.5 L, Automatic 4-spd, Regular Gasoline Compare 2000 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 18 City 21 Combined 26 Highway 2000 Mercury Cougar 6 cyl, 2.5 L, Manual 5-spd, Regular Gasoline Compare 2000 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 18 City 21 Combined 26 Highway 2000 Mercury Grand Marquis 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 2000 Mercury Grand Marquis View MPG Estimates Shared By Vehicle Owners 16 City 18 Combined 23 Highway 2000 Mercury Mountaineer 2WD 6 cyl, 4.0 L, Automatic 5-spd, Regular Gasoline

327

Gas Mileage of 2004 Vehicles by Mercury  

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

4 Mercury Vehicles 4 Mercury Vehicles EPA MPG MODEL City Comb Hwy 2004 Mercury Grand Marquis 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 2004 Mercury Grand Marquis View MPG Estimates Shared By Vehicle Owners 15 City 18 Combined 23 Highway 2004 Mercury Marauder 8 cyl, 4.6 L, Automatic 4-spd, Premium Gasoline Compare 2004 Mercury Marauder View MPG Estimates Shared By Vehicle Owners 15 City 17 Combined 21 Highway 2004 Mercury Monterey Wagon FWD 6 cyl, 4.2 L, Automatic 4-spd, Regular Gasoline Compare 2004 Mercury Monterey Wagon FWD View MPG Estimates Shared By Vehicle Owners 15 City 17 Combined 21 Highway 2004 Mercury Mountaineer 2WD 8 cyl, 4.6 L, Automatic 5-spd, Regular Gasoline Compare 2004 Mercury Mountaineer 2WD 13 City 15 Combined 18 Highway 2004 Mercury Mountaineer 2WD 6 cyl, 4.0 L, Automatic 5-spd, Regular Gasoline

328

Gas Mileage of 1997 Vehicles by Mercury  

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

7 Mercury Vehicles 7 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1997 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Regular Gasoline Compare 1997 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 16 City 19 Combined 24 Highway 1997 Mercury Cougar 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 1997 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 15 City 18 Combined 23 Highway 1997 Mercury Grand Marquis 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 1997 Mercury Grand Marquis View MPG Estimates Shared By Vehicle Owners 15 City 18 Combined 23 Highway 1997 Mercury Mountaineer 2WD 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1997 Mercury Mountaineer 2WD View MPG Estimates Shared By Vehicle Owners 12 City 14 Combined 17 Highway 1997 Mercury Mountaineer 4WD 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline

329

Gas Mileage of 1995 Vehicles by Mercury  

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

5 Mercury Vehicles 5 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1995 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Regular Gasoline Compare 1995 Mercury Cougar 17 City 19 Combined 24 Highway 1995 Mercury Cougar 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 1995 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 15 City 18 Combined 23 Highway 1995 Mercury Grand Marquis 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 1995 Mercury Grand Marquis View MPG Estimates Shared By Vehicle Owners 15 City 18 Combined 23 Highway 1995 Mercury Mystique 4 cyl, 2.0 L, Automatic 4-spd, Regular Gasoline Compare 1995 Mercury Mystique View MPG Estimates Shared By Vehicle Owners 21 City 24 Combined 29 Highway 1995 Mercury Mystique 6 cyl, 2.5 L, Automatic 4-spd, Regular Gasoline

330

Gas Mileage of 2001 Vehicles by Mercury  

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

1 Mercury Vehicles 1 Mercury Vehicles EPA MPG MODEL City Comb Hwy 2001 Mercury Cougar 4 cyl, 2.0 L, Manual 5-spd, Regular Gasoline Compare 2001 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 21 City 24 Combined 31 Highway 2001 Mercury Cougar 6 cyl, 2.5 L, Automatic 4-spd, Regular Gasoline Compare 2001 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 18 City 21 Combined 26 Highway 2001 Mercury Cougar 6 cyl, 2.5 L, Manual 5-spd, Regular Gasoline Compare 2001 Mercury Cougar View MPG Estimates Shared By Vehicle Owners 18 City 21 Combined 27 Highway 2001 Mercury Grand Marquis 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 2001 Mercury Grand Marquis View MPG Estimates Shared By Vehicle Owners 16 City 18 Combined 23 Highway 2001 Mercury Mountaineer 2WD 6 cyl, 4.0 L, Automatic 5-spd, Regular Gasoline

331

Gas Mileage of 1998 Vehicles by Mercury  

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

8 Mercury Vehicles 8 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1998 Mercury Grand Marquis 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 1998 Mercury Grand Marquis View MPG Estimates Shared By Vehicle Owners 15 City 18 Combined 22 Highway 1998 Mercury Mountaineer 2WD 6 cyl, 4.0 L, Automatic 5-spd, Regular Gasoline Compare 1998 Mercury Mountaineer 2WD View MPG Estimates Shared By Vehicle Owners 14 City 16 Combined 18 Highway 1998 Mercury Mountaineer 2WD 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline Compare 1998 Mercury Mountaineer 2WD 12 City 14 Combined 17 Highway 1998 Mercury Mountaineer 4WD 6 cyl, 4.0 L, Automatic 5-spd, Regular Gasoline Compare 1998 Mercury Mountaineer 4WD View MPG Estimates Shared By Vehicle Owners 14 City 15 Combined 18 Highway 1998 Mercury Mountaineer 4WD 8 cyl, 5.0 L, Automatic 4-spd, Regular Gasoline

332

Gas Mileage of 2005 Vehicles by Mercury  

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

5 Mercury Vehicles 5 Mercury Vehicles EPA MPG MODEL City Comb Hwy 2005 Mercury Grand Marquis 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 2005 Mercury Grand Marquis View MPG Estimates Shared By Vehicle Owners 16 City 19 Combined 23 Highway 2005 Mercury Mariner 2WD 4 cyl, 2.3 L, Automatic 4-spd, Regular Gasoline Compare 2005 Mercury Mariner 2WD View MPG Estimates Shared By Vehicle Owners 19 City 21 Combined 24 Highway 2005 Mercury Mariner 2WD 6 cyl, 3.0 L, Automatic 4-spd, Regular Gasoline Compare 2005 Mercury Mariner 2WD View MPG Estimates Shared By Vehicle Owners 17 City 19 Combined 23 Highway 2005 Mercury Mariner 4WD 4 cyl, 2.3 L, Automatic 4-spd, Regular Gasoline Compare 2005 Mercury Mariner 4WD 17 City 19 Combined 21 Highway 2005 Mercury Mariner 4WD 6 cyl, 3.0 L, Automatic 4-spd, Regular Gasoline

333

Wavelengths and oscillator strengths of Xe II from the UVES spectra of four HgMn stars  

E-Print Network [OSTI]

In spite of large overabundances of Xe II observed in numerous mercury-manganese (HgMn) stars, Xe II oscillator strengths are only available for a very limited number of transitions. As a consequence, several unidentified lines in the spectra of HgMn stars could be due to Xe II. In addition, some predicted Xe II lines are redshifted by about 0.1 A from stellar unidentified lines, raising the question about the wavelength accuracy of the Xe II line data available in the literature. For these reasons we investigated the Xe II lines lying in the 3900-4521 A, 4769-7542 A, and 7660-8000 A spectral ranges of four well-studied HgMn stars. We compared the Xe II wavelengths listed in the NIST database with the position of the lines observed in the high-resolution UVES spectrum of the xenon-overabundant, slowly rotating HgMn stars HR 6000, and we modified them when needed. We derived astrophysical oscillator strengths for all the Xe II observed lines and compared them with the literature values, when available. In this...

Yüce, K; Hubrig, S

2011-01-01T23:59:59.000Z

334

Nuclear shape coexistence: A study of the even-even Hg isotopes using the interacting boson model with configuration mixing  

E-Print Network [OSTI]

Background: The Po, Pb, Hg, and Pt region is known for the presence of coexisting structures that correspond to different particle-hole configurations in the Shell Model language or equivalently to nuclear shapes with different deformation. Purpose: We intend to study the configuration mixing phenomenon in the Hg isotopes and to understand how different observables are influenced by it. Method: We study in detail a long chain of mercury isotopes, $^{172-200}$Hg, using the interacting boson model with configuration mixing. The parameters of the Hamiltonians are fixed through a least square fit to the known energies and absolute B(E2) transition rates of states up to $3$ MeV. Results: We obtained the IBM-CM Hamiltonians and we calculate excitation energies, B(E2)'s, quadrupole shape invariants, wave functions, isotopic shifts, and mean field energy surfaces. Conclusions: We obtain a fairly good agreement with the experimental data for all the studied observables and we conclude that the Hamiltonian and the states we obtain constitute a good approximation to the Hg isotopes.

J. E. Garcia-Ramos; K. Heyde

2013-12-17T23:59:59.000Z

335

Syntrophs Dominate Sequences Associated with the Mercury Methylation-Related Gene hgcA in the Water Conservation Areas of the Florida Everglades  

Science Journals Connector (OSTI)

...great concern because of potential adverse impacts on human and wildlife health through mercury accumulation in aquatic food webs. We developed a new PCR primer set targeting hgcA, a gene encoding a corrinoid protein essential for Hg methylation across...

Hee-Sung Bae; Forrest E. Dierberg; Andrew Ogram

2014-08-08T23:59:59.000Z

336

NETL: Mercury Emissions Control Technologies - Pilot Testing of Mercury  

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

Testing of Mercury Oxidation Catalysts Project Summary Testing of Mercury Oxidation Catalysts Project Summary URS Group, Inc., Austin, TX, will demonstrate at the pilot scale the use of solid honeycomb catalysts to promote the oxidation of elemental mercury in the flue gas from coal combustion, and the use of a wet flue gas desulfurization (FGD) system downstream to remove the oxidized mercury at high efficiency. The project's pilot tests, conducted at electric generating plants using wet flue gas desulfurization systems and particulate collection systems, will be conducted for periods up to 14 months to provide data for future, full-scale designs. Mercury-oxidation potential will be measured periodically to provide long-term catalyst life data. The project is applicable to about 90,000 megawatts of generation capacity. Project partners are the Electric Power Research Institute, Palo Alto, CA, which will co-manage and co-fund the pilot tests, and five utilities.

337

NETL: Mercury Emissions Control Technologies - Evaluation of Mercury  

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

Control Technology Evaluation of Mercury Emissions from Coal-Fired Facilities w/ SCR and FGD Systems Control Technology Evaluation of Mercury Emissions from Coal-Fired Facilities w/ SCR and FGD Systems CONSOL is evaluating the mercury removal co-benefits achieved by SCR-FGD combi nations. Specific issues that will be addressed include the effects of SCR, catalyst degradation, and load changes on mercury oxidation and capture. This objective will be achieved by measuring mercury removal achieved by SCR-FGD combinations at ten plants with such equipment configurations. These plants include five with wet limestone, three wet lime, and two with dry scrubbing. Material balance will be conducted. Related Papers and Publications: Final Report - April 2006 [PDF-377KB] Topical Report # 11 - January 2006 [PDF-19MB] Topical Report # 9 - January 2006 [PDF-6MB]

338

Mercury-Related Materials Studies  

E-Print Network [OSTI]

. Pawel, "Assessment of Cavitation-Erosion Resistance of Potential Pump Impeller Materials for MercuryMercury-Related Materials Studies Van Graves IDS NF Ph M tiIDS-NF Phone Meeting Jan 26, 2010 ­ updated Feb 3, 2010 #12;ORNL Material Reports Reviewed · IDS-NF requested ORNL research any past SNS

McDonald, Kirk

339

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

340

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

Note: This page contains sample records for the topic "mercury hg sulfur" 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

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...

342

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

343

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

344

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.

345

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

346

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

347

Collection of atomic mercury by electrostatic precipitators  

Science Journals Connector (OSTI)

... Flameless atomic absorption spectroscopy was used to measure the difference in the mercury concentration of gas ...

O. M. G. NEWMAN; D. J. PALMER

1978-10-12T23:59:59.000Z

348

Atmospheric Chemistry, Modeling, and Biogeochemistry of Mercury  

E-Print Network [OSTI]

activities that release mercury to the atmosphere include coal burning, industrial processes, waste incine

349

Graphene-sulfur nanocomposites for rechargeable lithium-sulfur battery electrodes  

SciTech Connect (OSTI)

Rechargeable lithium-sulfur batteries having a cathode that includes a graphene-sulfur nanocomposite can exhibit improved characteristics. The graphene-sulfur nanocomposite can be characterized by graphene sheets with particles of sulfur adsorbed to the graphene sheets. The sulfur particles have an average diameter less than 50 nm..

Liu, Jun; Lemmon, John P; Yang, Zhenguo; Cao, Yuiliang; Li, Xiaolin

2014-06-17T23:59:59.000Z

350

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

351

Mercury Vapor (Kooten, 1987) | Open Energy Information  

Open Energy Info (EERE)

Mercury Vapor (Kooten, 1987) Mercury Vapor (Kooten, 1987) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor (Kooten, 1987) Exploration Activity Details Location Unspecified Exploration Technique Mercury Vapor Activity Date Usefulness useful DOE-funding Unknown Notes Surface soil-mercury surveys are an inexpensive and useful exploration tool for geothermal resources. ---- Surface geochemical surveys for mercury were conducted in 16 areas in 1979-1981 by ARCO Oil and Gas Company as part of its geothermal evaluation program. Three techniques used together have proved satisfactory in evaluating surface mercury data. These are contouring, histograms and cumulative frequency plots of the data. Contouring geochemical data and constructing histograms are standard

352

Sulfur minimization in bacterial leaching  

SciTech Connect (OSTI)

The production of sewage biosolids in Ontario in 1989 was estimated to be 7 million m{sup 3} of wet sludge per year. Of this amount, land application accounts for between 20 and 30% of the total. Unfortunately, the use of sewage biosolids on agricultural land is often prohibited because of heavy metal contamination of the biosolids. High cost and operational problems have made chemical methods of metal extraction unattractive. Consequently, microbiological methods of leaching of heavy metals have been studied for over a decade. A relatively simple microbiological process has been investigated in recent years in flask level experiments and recently in a semicontinuous system. The process exploits nonacidophilic and acidophilic indigenous thiobacilli to extract heavy metals from sewage biosolids. These thiobacilli use elemental sulfur as the energy source, producing sulfuric acid. However, the resulting decontaminated biosolids can cause environmental problems like acidification of the soil, when acid is generated from the residual sulfur in the biosolids. The present study examines the possibility of reducing the amount of sulfur added in batch and semicontinuous bacterial leaching systems, and maximizing sulfur oxidation efficiency, thereby reducing the residual sulfur in leached biosolids.

Seth, R.; Prasad, D.; Henry, J.G. [Univ. of Toronto, Ontario (Canada). Dept. of Civil Engineering

1996-11-01T23:59:59.000Z

353

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

354

Historical Interrelated Variations of Mercury and Aquatic Organic Matter in Lake Sediment Cores from a Subarctic Lake in Yukon, Canada: Further Evidence toward the Algal-Mercury Scavenging Hypothesis  

Science Journals Connector (OSTI)

Historical Interrelated Variations of Mercury and Aquatic Organic Matter in Lake Sediment Cores from a Subarctic Lake in Yukon, Canada: Further Evidence toward the Algal-Mercury Scavenging Hypothesis ... In recent sediments, S1 is a good indicator of the labile portion of algal-derived organic matter, but it is highly susceptible to the degradation exerted by selective diagenetic processes (by bacterial processes and/or oxidation). ... The pelagic-to-benthic process of algal scavenging of contaminants such as Hg in these lakes is exactly analogous to the well-known “biological pump” that operates in the world’s oceans to transfer carbon and trace elements including Hg from the upper oceanic water column to bottom waters and sediments (24). ...

G. A. Stern; H. Sanei; P. Roach; J. DeLaronde; P. M. Outridge

2009-09-21T23:59:59.000Z

355

Mercury and tritium removal from DOE waste oils  

SciTech Connect (OSTI)

This work covers the investigation of vacuum extraction as a means to remove tritiated contamination as well as the removal via sorption of dissolved mercury from contaminated oils. The radiation damage in oils from tritium causes production of hydrogen, methane, and low-molecular-weight hydrocarbons. When tritium gas is present in the oil, the tritium atom is incorporated into the formed hydrocarbons. The transformer industry measures gas content/composition of transformer oils as a diagnostic tool for the transformers` condition. The analytical approach (ASTM D3612-90) used for these measurements is vacuum extraction of all gases (H{sub 2}, N{sub 2}, O{sub 2}, CO, CO{sub 2}, etc.) followed by analysis of the evolved gas mixture. This extraction method will be adapted to remove dissolved gases (including tritium) from the SRS vacuum pump oil. It may be necessary to heat (60{degrees}C to 70{degrees}C) the oil during vacuum extraction to remove tritiated water. A method described in the procedures is a stripper column extraction, in which a carrier gas (argon) is used to remove dissolved gases from oil that is dispersed on high surface area beads. This method appears promising for scale-up as a treatment process, and a modified process is also being used as a dewatering technique by SD Myers, Inc. (a transformer consulting company) for transformers in the field by a mobile unit. Although some mercury may be removed during the vacuum extraction, the most common technique for removing mercury from oil is by using sulfur-impregnated activated carbon (SIAC). SIAC is currently being used by the petroleum industry to remove mercury from hydrocarbon mixtures, but the sorbent has not been previously tested on DOE vacuum oil waste. It is anticipated that a final process will be similar to technologies used by the petroleum industry and is comparable to ion exchange operations in large column-type reactors.

Klasson, E.T. [Oak Ridge National Lab., TN (United States)

1997-10-01T23:59:59.000Z

356

MESSENGER Observations of Magnetic Reconnection in Mercury’s Magnetosphere  

Science Journals Connector (OSTI)

...Prague 14131, Czech Republic. Solar wind energy transfer to planetary magnetospheres...MP reconnection transfers solar wind energy into the magnetosphere, where...Mercury's magnetosphere. | Solar wind energy transfer to planetary magnetospheres...

James A. Slavin; Mario H. Acuña; Brian J. Anderson; Daniel N. Baker; Mehdi Benna; Scott A. Boardsen; George Gloeckler; Robert E. Gold; George C. Ho; Haje Korth; Stamatios M. Krimigis; Ralph L. McNutt; Jr.; Jim M. Raines; Menelaos Sarantos; David Schriver; Sean C. Solomon; Pavel Trávní?ek; Thomas H. Zurbuchen

2009-05-01T23:59:59.000Z

357

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

358

Mercury's moment of inertia from spin and gravity data  

E-Print Network [OSTI]

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

2012-01-01T23:59:59.000Z

359

Magnetism of HgSe:Fe  

Science Journals Connector (OSTI)

The perpendicular and parallel components of the magnetization of the mixed valence system Hg1-xFexSe in the strongly dilute limit (xmagnetic fields up to 20 T. In this interesting semimagnetic semiconductor the overall magnetization is caused simultaneously by Fe3+ (Brillouin paramagnet), Fe2+ (van Vleck paramagnet), and free electrons (diamagnetic de Haas-van Alphen effect). Using a torque magnetometer the various contributions with their anisotropy are individually determined. For very low iron content (xmagnetic moment perpendicular to the magnetic field when applying the field in a nonsymmetric direction of the crystal. Using recent theoretical results on the energy-level diagram of Fe2+ in the Td symmetry of a HgSe host lattice we deduce a spin-orbit level splitting of 2 meV from our experimental data. In contrast to higher concentration samples, both the Brillouin paramagnetism of Fe3+ and the van Vleck paramagnetism of Fe2+ can be attributed to the sum from individual Fe donors with no obvious magnetic interaction between them. Finally, we also have measured de Haas-van Alphen oscillations of the conduction-band electrons with amplitudes of the same order as the paramagnetic background. From the measured crystal-field-induced anisotropy in the magnetic moment we deduce a Fermi-surface anisotropy of about 7%.

U. Zeitler; A. Wittlin; J. C. Maan; W. Dobrowolski; A. Mycielski

1996-12-01T23:59:59.000Z

360

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

Note: This page contains sample records for the topic "mercury hg sulfur" 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

Sulfur capture in combination bark boilers  

SciTech Connect (OSTI)

A review of sulfur dioxide emission data for eight combination bark boilers in conjunction with the sulfur contents of the fuels reveals significant sulfur capture ranging from 10% to over 80% within the solid ash phase. Wood ash characteristics similar to activated carbon as well as the significant wood ash alkali oxide and carbonate fractions are believed responsible for the sulfur capture. Sulfur emissions from combination bark-fossil fuel firing are correlated to the sulfur input per ton of bark or wood residue fired.

Someshwar, A.V.; Jain, A.K. (National Council of the Paper Industry for Air and Stream Improvement, Gainesville, FL (United States))

1993-07-01T23:59:59.000Z

362

Methylmercury and inorganic mercury in serum -- correlation to fish consumption and dental amalgam in a cohort of women born in 1922  

SciTech Connect (OSTI)

Methylmercury in serum (S-MeHg) was assessed from serum concentrations of total (S-TotHg) and inorganic mercury (S-InoHg), determined by cold vapor-atomic absorption spectrometry. The samples were collected from 135 women on two occasions, in 1968--1969 and 1980--1981. In a subgroup of 29 women, an association was found between S-MeHg and the amount of fish consumed in 1968--1969. The association was stronger when the individuals` mean S-MeHg from 1968--19659 and 1980--1981 were plotted vs fish consumption 1968--1969. In the group, as a whole, there was an association between S-InoHg and number of dental amalgam surfaces, in both 1968--1969 and 1980--1981. The S-InoHg increased by approximately 0.1 nmol/L per amalgam tooth surface, corresponding to an uptake of approximately 0.2 {micro}g/day per amalgam surface, but with considerable interindividual differences. The levels were lower in 1980--1981 than in 1968--1969 for both MeH and InoHg.

Bergdahl, I.A.; Schuetz, A. [Lund Univ. (Sweden). Dept. of Occupational and Environmental Medicine] [Lund Univ. (Sweden). Dept. of Occupational and Environmental Medicine; Ahlqwist, M. [Medicinargatan 12, Goeteborg (Sweden). Dept. of Oral Diagnostic Radiology] [Medicinargatan 12, Goeteborg (Sweden). Dept. of Oral Diagnostic Radiology; Bengtsson, C. [Goeteborg Univ. (Sweden). Vasa Hospital] [Goeteborg Univ. (Sweden). Vasa Hospital; Lissner, L. [Goeteborg Univ. (Sweden). Vasa Hospital] [Goeteborg Univ. (Sweden). Vasa Hospital; [Sahlgrenska Univ. Hospital, Goeteborg (Sweden). Dept. of Internal Medicine; Lapidus, L.; Hulten, B. [Sahlgrenska Univ. Hospital, Goeteborg (Sweden)] [Sahlgrenska Univ. Hospital, Goeteborg (Sweden)

1998-04-01T23:59:59.000Z

363

Hg Anomalies In Soils- A Geochemical Exploration Method For Geothermal  

Open Energy Info (EERE)

Hg Anomalies In Soils- A Geochemical Exploration Method For Geothermal Hg Anomalies In Soils- A Geochemical Exploration Method For Geothermal Areas Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Journal Article: Hg Anomalies In Soils- A Geochemical Exploration Method For Geothermal Areas Details Activities (5) Areas (5) Regions (0) Abstract: Hg contents of soils in geothermal areas in the western U.S. were measured and a three-fold distribution was observed: peak, aureole and background. Peak values (up to several 100 ppm Hg) occur in fumaroles of vapour-dominated systems, around hot springs, and in zones overlying steeply dipping, hot-water aquifers. Aureoic values (up to several 100 ppb Hg) are found in zones surrounding the peak areas and delineate areas with shallow geothermal convection. Background values vary between 7 and 40 ppb

364

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

365

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

366

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

367

Molecular Structures of Polymer/Sulfur Composites for Lithium...  

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

Structures of PolymerSulfur Composites for Lithium-Sulfur Batteries with Long Cycle Life. Molecular Structures of PolymerSulfur Composites for Lithium-Sulfur Batteries with Long...

368

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 Ã? 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

369

Amylopectin Wrapped Graphene Oxide/Sulfur for Improved Cyclability of Lithium–Sulfur Battery  

Science Journals Connector (OSTI)

Amylopectin Wrapped Graphene Oxide/Sulfur for Improved Cyclability of Lithium–Sulfur Battery ... An amylopectin wrapped graphene oxide-sulfur composite was prepared to construct a 3-dimensionally cross-linked structure through the interaction between amylopectin and graphene oxide, for stabilizing lithium sulfur batteries. ...

Weidong Zhou; Hao Chen; Yingchao Yu; Deli Wang; Zhiming Cui; Francis J. DiSalvo; Héctor D. Abruña

2013-09-05T23:59:59.000Z

370

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 106°C 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 Henry’s 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

371

NETL: Mercury Emissions Control Technologies - Mercury Control For Plants  

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

Mercury Control For Plants Firing Texas Lignite and Equipped with ESP-wet FGD Mercury Control For Plants Firing Texas Lignite and Equipped with ESP-wet FGD URS Group, Inc., in collaboration with EPRI, Apogee Scientific, AEP, Texas Genco, and TXU Power, ADA-ES, will evaluate sorbent injection for mercury control in an 85/15 blend Texas lignite/PRB derived flue gas, upstream of a cold-side ESP – wet FGD combination. Full-scale sorbent injection tests conducted with various sorbents and combinations of fuel and plant air pollution control devices (APCD) have provided a good understanding of variables that affect sorbent performance. However, many uncertainties exist regarding long-term performance and data gaps remain for specific plant configurations. For example, sorbent injection has not been demonstrated at full-scale for plants firing Texas lignite, which represent approximately 10% of the annual U.S. power plant mercury emissions. The low and variable chloride content of Texas lignite may pose a challenge to achieving high levels of mercury removal with sorbent injection. Furthermore, activated carbon injection may render the fly ash unsuitable for sale, posing an economic liability to Texas lignite utilities. Alternatives to standard activated carbon, such as non-carbon sorbents and alternate injection locations (Toxecon II), have not been fully explored. Toxecon II involves sorbent injection in the middle field(s) of an ESP, thus preserving the integrity of the fly ash in the first fields.

372

Sulfur: its clinical and toxicologic aspects  

Science Journals Connector (OSTI)

Although there is no known dietary requirement for inorganic sulfur, it is an essential element for all animal species in as much as they all require the sulfur-containing amino acid methionine. There are three predominate forms of organic sulfur in animals and humans: 1) the thiomethyl of methionine residues in protein; 2) the sulfhydryl disulfides of protein; and 3) the compounds containing ester or amide bound sulfates of glycosaminoglycans, steroids, and many xenobiotic metabolites. Thus, sulfur becomes an important constituent of amino acids, proteins, enzymes, vitamins and other biomolecules. Unlike mammalian species, plants can use inorganic sulfur and synthesize methionine from which are synthesized all the other important sulfur compounds. Hence, sulfur deficiency occurs mainly when plants are grown in sulfur-depleted soils and when humans and animals consume low-protein diets. In recent times, however, the increasing prevalence of refining petroleum and smelting sulfur compounds of metallic minerals into free metals are having a large impact on the balance of sulfur in the environment. Sulfur toxicity is associated mainly with high levels of the element and its toxic volatile substances in the environment. Sulfur dioxide (SO2), a major air pollutant, may adversely affect animal and human health by causing bronchitis, bronchoconstriction, and increased pulmonary resistance.

Lioudmila A Komarnisky; Robert J Christopherson; Tapan K Basu

2003-01-01T23:59:59.000Z

373

Two stage sorption of sulfur compounds  

DOE Patents [OSTI]

A two stage method for reducing the sulfur content of exhaust gases is disclosed. Alkali- or alkaline-earth-based sorbent is totally or partially vaporized and introduced into a sulfur-containing gas stream. The activated sorbent can be introduced in the reaction zone or the exhaust gases of a combustor or a gasifier. High efficiencies of sulfur removal can be achieved.

Moore, William E. (Manassas, VA)

1992-01-01T23:59:59.000Z

374

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

375

Mercury Solar Systems | Open Energy Information  

Open Energy Info (EERE)

commercial and residential clients in the New York metrotri-state area. References: Mercury Solar Systems1 This article is a stub. You can help OpenEI by expanding it. Mercury...

376

Evidence of stress?mediated Hg migration in Hg1?x Cd x Te  

Science Journals Connector (OSTI)

Photoemission results from some ?110? cleaved surfaces of Hg1?x Cd x Te indicate that the Fermi level is pinned suggesting that while the bulk of the material is p type the area stressed during cleavage has been converted to n type. Electrolyte electroreflectance (EER) measurement confirmed the n?type character of the cleaved surface and showed that the alloy composition x at the surface after cleavage is high (x=0.22) compared to the bulk value (x=0.185). The high x value associated with the n character indicates that under stress the Hg migrates at least partially via the formation of donor defects. The defect density is reflected in the EER linewidth.

P. M. Raccah; U. Lee; J. A. Silberman; W. E. Spicer; J. A. Wilson

1983-01-01T23:59:59.000Z

377

A Tragic Reminder about Organic Mercury  

Science Journals Connector (OSTI)

...politically contentious. Mercury is used in industry primarily in the manufacture of batteries, latex paint, urethane, and polyvinyl chloride. Pollution of the environment by mercury occurs mainly through incinerators, fossil-fuel plants, leaching from mining waste, and municipal sewage systems. Industrial discharge... Exposure to mercury and its potential toxic effects is a subject that involves everyone, because we are all frequently exposed. The toxicologic literature has clearly established the dangers of excessive exposure to mercury. What is less clear is the dose ...

Kulig K.

1998-06-04T23:59:59.000Z

378

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

379

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

380

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

Note: This page contains sample records for the topic "mercury hg sulfur" 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

Surface Mercury Geochemistry As A Guide To Volcanic Vent Structure And  

Open Energy Info (EERE)

source source History View New Pages Recent Changes All Special Pages Semantic Search/Querying Get Involved Help Apps Datasets Community Login | Sign Up Search Page Edit History Facebook icon Twitter icon » Surface Mercury Geochemistry As A Guide To Volcanic Vent Structure And Zones Of High Heat Flow In The Valley Of Ten Thousand Smokes, Katmai National Park, Alaska Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Journal Article: Surface Mercury Geochemistry As A Guide To Volcanic Vent Structure And Zones Of High Heat Flow In The Valley Of Ten Thousand Smokes, Katmai National Park, Alaska Details Activities (2) Areas (1) Regions (0) Abstract: A reconnaissance survey of Hg° was designed to model the 1912 Novarupta vent structure and delineate zones of near-surface high heat

382

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

383

Toxecon Retrofit for Mercury and Mulit-Pollutant Control on Three 90-MW Coal-Fired Boilers  

SciTech Connect (OSTI)

This U.S. Department of Energy (DOE) Clean Coal Power Initiative (CCPI) project was based on a cooperative agreement between We Energies and the DOE Office of Fossil Energy's National Energy Technology Laboratory (NETL) to design, install, evaluate, and demonstrate the EPRI-patented TOXECON{trademark} air pollution control process. Project partners included Cummins & Barnard, ADA-ES, and the Electric Power Research Institute (EPRI). The primary goal of this project was to reduce mercury emissions from three 90-MW units that burn Powder River Basin coal at the We Energies Presque Isle Power Plant in Marquette, Michigan. Additional goals were to reduce nitrogen oxide (NO{sub x}), sulfur dioxide (SO{sub 2}), and particulate matter emissions; allow reuse and sale of fly ash; advance commercialization of the technology; demonstrate a reliable mercury continuous emission monitor (CEM) suitable for use at power plants; and demonstrate recovery of mercury from the sorbent. Mercury was controlled by injection of activated carbon upstream of the TOXECON{trademark} baghouse, which achieved more than 90% removal on average over a 44-month period. During a two-week test involving trona injection, SO{sub 2} emissions were reduced by 70%, although no coincident removal of NOx was achieved. The TOXECON{trademark} baghouse also provided enhanced particulate control, particularly during startup of the boilers. On this project, mercury CEMs were developed and tested in collaboration with Thermo Fisher Scientific, resulting in a reliable CEM that could be used in the power plant environment and that could measure mercury as low as 0.1 {micro}g/m{sup 3}. Sorbents were injected downstream of the primary particulate collection device, allowing for continued sale and beneficial use of captured fly ash. Two methods for recovering mercury using thermal desorption on the TOXECON{trademark} PAC/ash mixture were successfully tested during this program. Two methods for using the TOXECON{trademark} PAC/ash mixture in structural concrete were also successfully developed and tested. This project demonstrated a significant reduction in the rate of emissions from Presque Isle Units 7, 8, and 9, and substantial progress toward establishing the design criteria for one of the most promising mercury control retrofit technologies currently available. The Levelized Cost for 90% mercury removal at this site was calculated at $77,031 per pound of mercury removed with a capital cost of $63,189 per pound of mercury removed. Mercury removal at the Presque Isle Power Plant averages approximately 97 pounds per year.

Steven Derenne; Robin Stewart

2009-09-30T23:59:59.000Z

384

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

385

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

386

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

387

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

388

Mercury Pollution in the Marine Environment  

E-Print Network [OSTI]

Collaborative December 2012 SourceSto Seafood SourceSto Seafood #12;About the report In 2010, the Toxic Metals.P. Mason, L.R. Rardin, C.V. Schmitt, N.S. Serrell, and E.M. Sunderland. 2012. Sources to Seafood: Mercury. 2 Sources to Seafood: Mercury Pollution in the Marine Environment #12;Executive Summary Mercury

Shepherd, Simon

389

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

390

DOE/NETL's Mercury Control Technology R&D Program Review  

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

DOE/NETL's Mercury Control Technology R&D Program Review DOE/NETL's Mercury Control Technology R&D Program Review July 14-15, 2004 Table of Contents Disclaimer Papers and Presentations Program Review Overview Sorbent Injection Research Panel Discussion: Sorbent Injection for Hg Control Mercury Control Technology R&D I Poster Session Mercury Control Technology R&D II By-Product Characterization Disclaimer This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government or any agency thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise does not necessarily constitute or imply its endorsement, recommendation, or favoring by the United States Government or any agency thereof. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof.

391

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

392

Why Sequence Sulfur-Oxidizing Bacteria?  

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

Sulfur-Oxidizing Bacteria? Sulfur-Oxidizing Bacteria? Several environmental problems, such as acid rain, biocorrosion, etc., are caused by sulfur compounds, such as sulfur dioxide (SO2) and hydrogen sulfide (H2S). A sustainable process to remove these sulfur compounds is the production of elemental sulfur from H2S-containing gas streams by the use of sulfide-oxidizing bacteria. In this process, H2S is absorbed into the alkaline solution in the scrubber unit, followed by the biological oxidation of H2S to elemental sulfur and the recycling of water. With this two-step process, a variety of gas streams (i.e., natural gas, synthesis gas, biogas, and refinery gas) can be treated. For the treatment of sulfate-containing waste streams, an extra step has to be introduced: the transformation of sulfate into H2S by sulfate-reducing bacteria. In

393

DFJ Mercury | Open Energy Information  

Open Energy Info (EERE)

DFJ Mercury DFJ Mercury Jump to: navigation, search Name DFJ Mercury Place Houston, Texas Zip 77046 Product Houston-based seed and early-stage venture capital firm that targets the information technology, advanced materials, and bioscience sectors. Coordinates 29.76045°, -95.369784° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":29.76045,"lon":-95.369784,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

394

ENHANCED CONTROL OF MERCURY BY WET FLUE GAS DESULFURIZATION SYSTEMS  

SciTech Connect (OSTI)

The U.S. Department of Energy and EPRI co-funded this project to improve the control of mercury emissions from coal-fired power plants equipped with wet flue gas desulfurization (FGD) systems. The project has investigated catalytic oxidation of vapor-phase elemental mercury to a form that is more effectively captured in wet FGD systems. If successfully developed, the process could be applicable to over 90,000 MW of utility generating capacity with existing FGD systems, and to future FGD installations. Field tests were conducted to determine whether candidate catalyst materials remain active towards mercury oxidation after extended flue gas exposure. Catalyst life will have a large impact on the cost effectiveness of this potential process. A mobile catalyst test unit was used to test the activity of four different catalyst materials for a period of up to six months each at three utility sites. Catalyst testing was completed at the first site, which fires Texas lignite, in December 1998; at the second test site, which fires a Powder River Basin subbituminous coal, in November 1999; and at the third site, which fires a medium- to high-sulfur bituminous coal, in January 2001. Results of testing at each of the three sites were reported in previous technical notes. At Site 1, catalysts were tested only as powders dispersed in sand bed reactors. At Sites 2 and 3, catalysts were tested in two forms, including powders dispersed in sand and in commercially available forms such as extruded pellets and coated honeycomb structures. This final report summarizes and presents results from all three sites, for the various catalyst forms tested. Field testing was supported by laboratory tests to screen catalysts for activity at specific flue gas compositions, to investigate catalyst deactivation mechanisms and methods for regenerating spent catalysts. Laboratory results are also summarized and discussed in this report.

Unknown

2001-06-01T23:59:59.000Z

395

Long-Term Column Leaching of Phase II Mercury Control Technology By-Products  

SciTech Connect (OSTI)

An NETL research, development and demonstration program under DOE/Fossil Energy Innovations for Existing Plants is directed toward the improvement of the performance and economics of mercury control from coal-fired plants. The current Phase II of the RD&D program emphasizes the evaluation of performance and cost of control technologies through slip-stream and full scale field testing while continuing the development of novel concepts. One of the concerns of the NETL program is the fate of the captured flue gas mercury which is transferred to the condensed phase by-product stream. The stability of mercury and any co-captured elements in the by-products could have a large economic impact if it reduced by-product sales or increasing their disposal costs. As part of a greater characterization effort of Phase II facility baseline and control technology sample pairs, NETL in-house laboratories have performed continuous leaching of a select subset of the available sample pairs using four leachants: water (pH=5.7), dilute sulfuric acid (pH=1.2), dilute acetic acid (pH=2.9), and sodium carbonate (pH=11.1). This report describes results obtained for mercury, arsenic, and selenium during the 5-month leaching experiments.

Schroeder, K.T.; Cardone, C.R.; White, Fredrick; Rohar, P.C.; Kim, A.G

2007-07-01T23:59:59.000Z

396

Associations of prenatal maternal blood mercury concentrations with early and mid-childhood blood pressure: A prospective study  

Science Journals Connector (OSTI)

AbstractBackground Childhood blood pressure (BP) is an important determinant of adult cardiovascular disease. Prenatal exposure to methylmercury through maternal fish consumption has been reported to increase the BP of children years later. Methods Mother–child pairs were enrolled from Project Viva, a prospective cohort study in Massachusetts. From second trimester maternal blood samples, we measured erythrocyte mercury concentration. Systolic BP in children, measured up to 5 times per visit in early and mid-childhood (median ages 3.2 and 7.7 years), was the primary outcome. We used mixed-effect regression models to account for variation in the number of BP measurements and to average effects over both time points. Results Among 1103 mother–child pairs, mean (SD) second trimester total erythrocyte mercury concentration was 4.0 (3.9) ng/g among mothers whose children were assessed in early childhood and 4.0 (4.0) ng/g for children assessed in mid-childhood. Mean (SD) offspring systolic BP was 92.1 (10.4) mm Hg in early childhood and 94.3 (8.4) mm Hg in mid-childhood. After adjusting for mother and infant characteristics, mean second trimester blood mercury concentration was not associated with child systolic BP (regression coefficient, 0.1 mm Hg; 95% CI, ?1.3 to 1.5 for quartile 4 vs. quartile 1) at either time period. Further adjusting for second trimester maternal fish consumption, as well as docosahexaenoic acid and eicosapentaenoic acid consumption, did not substantially change the estimates. Conclusions The results of this study demonstrate an absence of association between childhood blood pressure and low-level mercury exposure typical of the general US population.

Brian T. Kalish; Sheryl L. Rifas-Shiman; Robert O. Wright; Chitra J. Amarasiriwardena; Innocent Jayawardene; Matthew W. Gillman; Steven E. Lipshultz; Emily Oken

2014-01-01T23:59:59.000Z

397

NETL: Mercury Emissions Control Technologies - Advanced Mercury Sorbents  

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

Advanced Mercury Sorbents with Low Impact on Power Plant Operations Advanced Mercury Sorbents with Low Impact on Power Plant Operations Apogee Scientific, Inc. (Apogee) will lead a Team comprised of Southern Company Services, TXU, Tennessee Valley Authority, EPRI, URS Group, University of Illinois-Illinois State Geological Survey (ISGS), Southern Research Institute (SRI), Calgon Carbon, and TDA Research, Inc., to evaluate a number of advanced sorbents for removing vapor-phase mercury from coal-fired flue gas that have minimal impact on by-product utilization and/or on existing particulate collection devices (PCD). The main objective of this program is to evaluate several advanced sorbents for removing mercury from coal-fired flue gas while posing minimal impact on plant operations through three advanced sorbent concepts: 1) Sorbents which minimize impact on concrete production through selective chemical passivation of activated carbon and use of non-carbon material, 2) sorbents that minimize baghouse pressure drop and ESP emissions, and 3) sorbents that can be recovered and reused.

398

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.

399

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

Broader source: Energy.gov (indexed) [DOE]

CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries 2011 DOE...

400

Chemical Form Matters: Differential Accumulation of Mercury Following Inorganic and Organic Mercury Exposures in Zebrafish Larvae  

SciTech Connect (OSTI)

Mercury, one of the most toxic elements, exists in various chemical forms each with different toxicities and health implications. Some methylated mercury forms, one of which exists in fish and other seafood products, pose a potential threat, especially during embryonic and early postnatal development. Despite global concerns, little is known about the mechanisms underlying transport and toxicity of different mercury species. To investigate the impact of different mercury chemical forms on vertebrate development, we have successfully combined the zebrafish, a well-established developmental biology model system, with synchrotron-based X-ray fluorescence imaging. Our work revealed substantial differences in tissue-specific accumulation patterns of mercury in zebrafish larvae exposed to four different mercury formulations in water. Methylmercury species not only resulted in overall higher mercury burdens but also targeted different cells and tissues than their inorganic counterparts, thus revealing a significant role of speciation in cellular and molecular targeting and mercury sequestration. For methylmercury species, the highest mercury concentrations were in the eye lens epithelial cells, independent of the formulation ligand (chloride versus L-cysteine). For inorganic mercury species, in absence of L-cysteine, the olfactory epithelium and kidney accumulated the greatest amounts of mercury. However, with L-cysteine present in the treatment solution, mercuric bis-L-cysteineate species dominated the treatment, significantly decreasing uptake. Our results clearly demonstrate that the common differentiation between organic and inorganic mercury is not sufficient to determine the toxicity of various mercury species.

Korbas, Malgorzata; MacDonald, Tracy C.; Pickering, Ingrid J.; George, Graham N.; Krone, Patrick H. (Saskatchewan)

2013-04-08T23:59:59.000Z

Note: This page contains sample records for the topic "mercury hg sulfur" 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

Improve reformer operation with trace sulfur removal  

SciTech Connect (OSTI)

Modern bimetallic reforming catalysts typically have feed specifications for sulfur of 0.5 to 1 wppm in the reformer naphtha carge. Sulfur in the raw naphtha is reduced to this level by naphtha hydrotreating. While most naphtha hydrotreating operations can usually obtain these levels without substantial problems. It is difficult to obtain levels much below 0.5 to 1 wppm with this process. Revamp of a constrained existing hydrotreater to reduce product sulfur slightly can be extremely costly typically entailing replacement or addition of a new reactor. At Engelhard the authors demonstrated that if the last traces of sulfur remaining from hydrotreating can be removed, the resulting ultra-low sulfur feed greatly improves the reformer operation and provides substantial economic benefit to the refiner. Removal of the remaining trace sulfur is accomplished in a simple manner with a special adsorbent bed, without adding complexity to the reforming operation.

McClung, R.G.; Novak, W.J.

1987-01-01T23:59:59.000Z

402

Theory and Experiments Relating to the Striated Glow Discharge in Mercury Vapor  

Science Journals Connector (OSTI)

Theory of the glow discharge in a monatomic gas.—For the case of parallel plane electrodes with a hot cathode as source of electrons, the potential distribution and ion concentration in the Crookes dark space, negative glow, Faraday dark space and positive column are shown to be predictable from considerations of space charge and of ionization and excitation of the gas. While with weak currents there is a negative space charge throughout, sufficiently intense ionization is shown to lead to a cathode drop, followed by a region of reversed electric field in which positive ions and electrons both move toward the anode by diffusion, owing to their large concentration gradient. Still farther from the cathode the field changes to its normal direction and increases up to the positive column. In the positive column the field and concentration are uniform unless atoms excited by electron impacts in certain layers are prevented from diffusing between the layers, when striations may be obtained with periodic changes of field and of concentration. The cathode edge of each striation has a positive space charge. The theory of the arc discharge is essentially the same, the arc being simply the negative glow of the longer glow discharge.Glow discharge in mercury vapor.—Various predictions of the above theory were verified by experiments with Hg vapor in vacuum tubes provided with hot cathodes. (1) Potential distribution and ion concentration were investigated by Langmuir's modified probe method and found to agree with the theoretical deductions, except that the concentration of positive ions in the positive column comes out too large. This result indicates the presence of negative mercury ions. (2) The distribution of velocities of electrons is Maxwellian except between striations. (3) The emission of light seems associated more with excitation by electron collision than with ionization and recombination. (4) Conditions for existence of striations. Striations are not found in pure Hg vapor unless the current is small or some substance like H2 is introduced to remove excited atoms. (5) The presence of atomic hydrogen which should be produced in the process of removing excited Hg atoms was proved by use of tungsten oxide. (6) Introduction of He, which cannot remove excited atoms, does not tend to produce striations. (7) The relative concentrations of excited atoms was determined from the optical absorption of subordinate series Hg lines. It was found that excited atoms exist in striations but not in the regions between, and are more numerous if the amount of H2 impurity is reduced.Band spectrum of HgH seems associated with the action of excited Hg atoms on hydrogen, and is emitted as a result of inelastic collisions in striations.

K. T. Compton; Louis A. Turner; W. H. McCurdy

1924-12-01T23:59:59.000Z

403

TOXECON RETROFIT FOR MERCURY AND MULTI-POLLUTANT CONTROL ON THREE 90 MW COAL FIRED BOILERS  

SciTech Connect (OSTI)

With the Nation's coal-burning utilities facing tighter controls on mercury pollutants, the U.S. Department of Energy is supporting projects that could offer power plant operators better ways to reduce these emissions at much lower costs. Sorbent injection technology represents one of the simplest and most mature approaches to controlling mercury emissions from coal-fired boilers. It involves injecting a solid material such as powdered activated carbon into the flue gas. The gas-phase mercury in the flue gas contacts the sorbent and attaches to its surface. The sorbent with the mercury attached is then collected by a particle control device along with the other solid material, primarily fly ash. WE Energies has over 3,700 MW of coal-fired generating capacity and supports an integrated multi-emission control strategy for SO{sub 2}, NO{sub x} and mercury emissions while maintaining a varied fuel mix for electric supply. The primary goal of this project is to reduce mercury emissions from three 90 MW units that burn Powder River Basin coal at the WE Energies Presque Isle Power Plant. Additional goals are to reduce nitrogen oxide (NO{sub x}), sulfur dioxide (SO{sub 2}), and particulate matter (PM) emissions, allow for reuse and sale of fly ash, demonstrate a reliable mercury continuous emission monitor (CEM) suitable for use in the power plant environment, and demonstrate a process to recover mercury captured in the sorbent. To achieve these goals, WE Energies (the Participant) will design, install, and operate a TOXECON{trademark} (TOXECON) system designed to clean the combined flue gases of units 7, 8, and 9 at the Presque Isle Power Plant. TOXECON is a patented process in which a fabric filter system (baghouse) installed down stream of an existing particle control device is used in conjunction with sorbent injection for removal of pollutants from combustion flue gas. For this project, the flue gas emissions will be controlled from the three units using a single baghouse. Mercury will be controlled by injection of activated carbon or other novel sorbents, while NO{sub x} and SO{sub 2} will be controlled by injection of sodium based or other novel sorbents. Addition of the TOXECON baghouse will provide enhanced particulate control. Sorbents will be injected downstream of the existing particle collection device to allow for continued sale and reuse of captured fly ash from the existing particulate control device, uncontaminated by activated carbon or sodium sorbents. Methods for sorbent regeneration, i.e. mercury recovery from the sorbent, will be explored and evaluated. For mercury concentration monitoring in the flue gas streams, components available for use will be evaluated and the best available will be integrated into a mercury CEM suitable for use in the power plant environment. This project will provide for the use of a novel multi-pollutant control system to reduce emissions of mercury and other air pollutants, while minimizing waste, from a coal-fired power generation system.

Richard E. Johnson

2004-07-30T23:59:59.000Z

404

Distribution of hazardous air pollutant trace elements, total sulfur, and ash in coals from five Tertiary basins in the Rocky Mountain Region  

SciTech Connect (OSTI)

Arithmetic mean values of the contents of hazardous air pollutant (HAP) trace elements named in the 1990 Clean Air Act Amendments (antimony, arsenic, beryllium, cadmium, chromium, cobalt, lead, manganese, mercury, nickel, selenium, and uranium), ash, and total sulfur were statistically compared on a whole-coal basis for Paleocene coals from five Tertiary basins in the Rocky Mountain Region. The study of proximate and elemental analyses indicate a relationship between trace element contents and paleogeography.

Ellis, M.S.; Stricker, G.D.; Flores, R.M. [Geological Survey, Denver, CO (United States)

1994-12-31T23:59:59.000Z

405

Contribution of isotopologue self-shielding to sulfur mass-independent fractionation during sulfur dioxide photolysis  

E-Print Network [OSTI]

Signatures of sulfur mass-independent fractionation (S-MIF) are observed for sulfur minerals in Archean rocks, and for modern stratospheric sulfate aerosols (SSA) deposited in polar ice. Ultraviolet light photolysis of ...

Lyons, J. R.

406

HYDROCARBON AND SULFUR SENSORS FOR SOFC SYSTEMS  

SciTech Connect (OSTI)

The following report summarizes work conducted during the Phase I program Hydrocarbon and Sulfur Sensors for SOFC Systems under contract No. DE-FC26-02NT41576. For the SOFC application, sensors are required to monitor hydrocarbons and sulfur in order to increase the operation life of SOFC components. This report discusses the development of two such sensors, one based on thick film approach for sulfur monitoring and the second galvanic based for hydrocarbon monitoring.

A.M. Azad; Chris Holt; Todd Lesousky; Scott Swartz

2003-11-01T23:59:59.000Z

407

A Mercury orientation model including non-zero obliquity and librations  

E-Print Network [OSTI]

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

Margot, Jean-Luc

2009-01-01T23:59:59.000Z

408

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

409

Mercury Surface, Space Environment, Geochemistry, and Ranging Mission  

E-Print Network [OSTI]

MESSENGER Mercury Surface, Space Environment, Geochemistry, and Ranging Mission Frequently Asked Mercury's characteristics and environment during two complementary mission phases. The mission's primary goal is to increase our understanding of Mercury's density, geologic history, magnetic field, core

Mojzsis, Stephen J.

410

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

411

Determination of Mercury in Soils by Flameless Atomic Absorption Spectrometry  

Science Journals Connector (OSTI)

...chemical analysis exploration flameless geochemical methods mercury...Determination of Mercury in Soils by Flameless Atomic Absorption Spectrometry...Determinationof Mercury in Soilsby Flameless Atomic AbsorptionSpectrometry...the mercuryre- RF Induction Heater work coils 1. Carriergas...

B. G. Weissberg

412

Sulfur-Free Selective Pulping  

E-Print Network [OSTI]

Technoeconomic Appraisal," December 1991. 5. DOE Annual Report on Contract No. AC02-83CH10093, Bozell, J. J., Hames, B., Chum, H. L., Dimmel, D. R, Althen, E., Caldwell, P. L., Daube, Oxidation ;; Diels-Alder .. I I -Methanol .. ~ 5 I 3 (C~O) OCH... - Hydrogen 3 (Q-IP) # Q-I 3 o o ~ o 1 2 ~ (H) Lignin DMBQ =two OCH3 groups Anthraquinone MMBQ =one OCH3 group A. K, and Kuroda, K-I.,"Sulfur-free Selective Pulping," March 1992. 6. DOE Annual Report on Contrac No. DE-AC02-83CH10093, Bozell, J. J...

Dimmel, D. R.; Bozell, J. J.

413

COST OF MERCURY REMOVAL IN IGCC PLANTS  

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

Cost of Mercury Removal Cost of Mercury Removal in an IGCC Plant Final Report September 2002 Prepared for: The United States Department of Energy National Energy Technology Laboratory By: Parsons Infrastructure and Technology Group Inc. Reading, Pennsylvania Pittsburgh, Pennsylvania DOE Product Manager: Gary J. Stiegel DOE Task Manager: James R. Longanbach Principal Investigators: Michael G. Klett Russell C. Maxwell Michael D. Rutkowski PARSONS The Cost of Mercury Removal in an IGCC Plant Final Report i September 2002 TABLE OF CONTENTS Section Title Page 1 Summary 1 2 Introduction 3 3 Background 4 3.1 Regulatory Initiatives 4 3.2 Mercury Removal for Conventional Coal-Fired Plants 4 3.3 Mercury Removal Experience in Gasification 5 3.4 Variability of Mercury Content in Coal 6 4 Design Considerations 7 4.1 Carbon Bed Location

414

Assessment of Low Cost Novel Mercury Sorbents  

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

Testing of Mercury Control Technologies Testing of Mercury Control Technologies for Coal-Fired Power Plants by Thomas J. Feeley, III 1. , Lynn A. Brickett 1. , B. Andrew O'Palko 1. , and James T. Murphy 2. 1. U.S. Department of Energy, National Energy Technology Laboratory 2. Science Applications International Corporation The U.S. Department of Energy/National Energy Technology Laboratory (DOE/NETL) is conducting a comprehensive research, development, and demonstration (RD&D) program directed at advancing the performance and economics of mercury control technologies for coal- fired power plants. The program also includes evaluating the fate of mercury in coal by-products and studying the transport and transformation of mercury in power plant plumes. This paper presents results from ongoing full-scale and slip-stream field testing of several mercury control

415

Graphene-wrapped sulfur nanospheres with ultra-high sulfur loading for high energy density lithium–sulfur batteries  

Science Journals Connector (OSTI)

Abstract Lithium–sulfur (Li–S) battery with high theoretical energy density is one of the most promising energy storage systems for electric vehicles and intermittent renewable energy. However, due to the poor conductivity of the active material, considerable weight of the electrode is occupied by the conductive additives. Here we report a graphene-wrapped sulfur nanospheres composite (S-nanosphere@G) with sulfur content up to 91 wt% as the high energy density cathode material for Li–S battery. The sulfur nanospheres with diameter of 400–500 nm are synthesized through a solution-based approach with the existence of polyvinylpyrrolidone (PVP). Then the sulfur nanospheres are uniformly wrapped by conductive graphene sheets through the electrostatic interaction between graphene oxide and PVP, followed by reducing of graphene oxide with hydrazine. The design of graphene wrapped sulfur nanoarchitecture provides flexible conductive graphene coating with void space to accommodate the volume expansion of sulfur and to minimize polysulfide dissolution. As a result, the S-nanosphere@G nanocomposite with 91 wt% sulfur shows a reversible initial capacity of 970 mA h g?1 and an average columbic efficiency > 96% over 100 cycles at a rate of 0.2 C. Taking the total mass of electrode into account, the S-nanosphere@G composite is a promising cathode material for high energy density Li–S batteries.

Ya Liu; Jinxin Guo; Jun Zhang; Qingmei Su; Gaohui Du

2015-01-01T23:59:59.000Z

416

Mercury Replacement Program It is the policy of California State University, Fullerton to remove mercury containing  

E-Print Network [OSTI]

Mercury Replacement Program I. Policy It is the policy of California State University, Fullerton to remove mercury containing devices throughout campus, insofar as is reasonably possible, and provide, the University has an obligation to safeguard employees from the potential health effects of mercury vapor while

de Lijser, Peter