Powered by Deep Web Technologies
Note: This page contains sample records for the topic "trace elements 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

It's Elemental - The Element Sulfur  

NLE Websites -- All DOE Office Websites (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

2

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

3

It's Elemental - Isotopes of the Element Sulfur  

NLE Websites -- All DOE Office Websites (Extended Search)

Phosphorus Previous Element (Phosphorus) The Periodic Table of Elements Next Element (Chlorine) Chlorine Isotopes of the Element Sulfur Click for Main Data Most of the isotope...

4

Trace element emissions  

SciTech Connect

The Energy & Environmental Research Center (EERC) is carrying out an investigation that will provide methods to predict the fate of selected trace elements in integrated gasification combined cycle (IGCC) and integrated gasification fuel cell (IGFC) systems to aid in the development of methods to control the emission of trace elements determined to be air toxics. The goal of this project is to identify the effects of critical chemical and physical transformations associated with trace element behavior in IGCC and IGFC systems. The trace elements included in this project are arsenic, chromium, cadmium, mercury, nickel, selenium, and lead. The research seeks to identify and fill, experimentally and/or theoretically, data gaps that currently exist on the fate and composition of trace elements. The specific objectives are to (1) review the existing literature to identify the type and quantity of trace elements from coal gasification systems, (2) perform laboratory-scale experimentation and computer modeling to enable prediction of trace element emissions, and (3) identify methods to control trace element emissions.

Benson, S.A.; Erickson, T.A.; Steadman, E.N.; Zygarlicke, C.J.; Hauserman, W.B.; Hassett, D.J.

1994-10-01T23:59:59.000Z

5

Multimedia Trace Elements Measurements  

Science Conference Proceedings (OSTI)

Current and future trace element regulations on flue gas emissions, water discharges, and solid waste disposal will result in increasingly stringent limits and substantially increased costs for energy companies. As a result, there is a critical need to address environmental pollutant releases in a holistic, multimedia manner so that a pollutant removed by a control technology in one medium (for example, flue gas) is properly managed in regard to discharges in the other media (water and solid waste). This...

2008-03-25T23:59:59.000Z

6

Hydrogen sulfide, trace element and sulfur hexafluoride tracer treatment from the Geysers-Calistoga Geothermal Resource Area based on aircraft and surface sampling  

DOE Green Energy (OSTI)

This four-day study has provided initial data regarding the short-range transport of pollutants from The Geysers geothermal operations. The initial analysis of the data has shown that a measureable plume of gaseous sulfur (H{sub 2}S) is emitted from the Geysers and transported by surface and upper-level winds to distances beyond 20 km. Only one day had concentrations above 30 ppB and on this day H{sub 2}S was detected as a distinct odor at 1500 m (m.s.1.) at 4 km or more from the Geysers. The initial data analysis of the H{sub 2}S and SF{sub 6} plume data have revealed the important role that vertical wind shear plays in changing plume trajectories with height and enhancing diffusion of pollutants. Surface and aircraft sampling of aerosols indicate that small quantities of trace elements such as As, Cd, Hg, Pb, Cr and Br may be transported from the area.

Orgill, M.M.; Lee, R.N.; Nickola, P.W.; Schreck, R.C.

1983-05-01T23:59:59.000Z

7

Catalyst for elemental sulfur recovery process  

DOE Patents (OSTI)

A catalytic reduction process is described for the direct recovery of elemental sulfur from various SO[sub 2]-containing industrial gas streams. The catalytic process provides high activity and selectivity, as well as stability in the reaction atmosphere, 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 a metal oxide composite catalyst having one of the following empirical formulas: [(FO[sub 2])[sub 1[minus]n](RO)[sub n

Flytzani-Stephanopoulos, M.; Liu, W.

1995-01-24T23:59:59.000Z

8

Phytoremediation of Trace Elements by Wetland Plants  

Science Conference Proceedings (OSTI)

Some plants naturally absorb and hyperaccumulate trace elements in their tissues. In a process known as phytoremediation, scientists are harnessing this ability to remove toxic heavy metals and trace elements from contaminated soils and waters. This screening program quantified the capacity of various wetland plant species for removing trace elements from polluted water.

2001-08-23T23:59:59.000Z

9

TRACE ELEMENT ANALYSES OF URANIUM MATERIALS  

SciTech Connect

The Savannah River National Laboratory (SRNL) has developed an analytical method to measure many trace elements in a variety of uranium materials at the high part-per-billion (ppb) to low part-per-million (ppm) levels using matrix removal and analysis by quadrapole ICP-MS. Over 35 elements were measured in uranium oxides, acetate, ore and metal. Replicate analyses of samples did provide precise results however none of the materials was certified for trace element content thus no measure of the accuracy could be made. The DOE New Brunswick Laboratory (NBL) does provide a Certified Reference Material (CRM) that has provisional values for a series of trace elements. The NBL CRM were purchased and analyzed to determine the accuracy of the method for the analysis of trace elements in uranium oxide. These results are presented and discussed in the following paper.

Beals, D; Charles Shick, C

2008-06-09T23:59:59.000Z

10

Trace Element Analysis | Open Energy Information  

Open Energy Info (EERE)

Trace Element Analysis Trace Element Analysis Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Technique: Trace Element Analysis Details Activities (8) Areas (8) Regions (4) 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: Hydrological: Reconstructing the fluid circulation of a hydrothermal system Thermal: Cost Information Low-End Estimate (USD): 15.001,500 centUSD 0.015 kUSD 1.5e-5 MUSD 1.5e-8 TUSD / element Median Estimate (USD): 18.001,800 centUSD 0.018 kUSD 1.8e-5 MUSD 1.8e-8 TUSD / element High-End Estimate (USD): 106.0010,600 centUSD 0.106 kUSD 1.06e-4 MUSD 1.06e-7 TUSD / element

11

Method for removing sulfur oxide from waste gases and recovering elemental sulfur  

DOE Patents (OSTI)

A continuous catalytic fused salt extraction process is described for removing sulfur oxides from gaseous streams. The gaseous stream is contacted with a molten potassium sulfate salt mixture having a dissolved catalyst to oxidize sulfur dioxide to sulfur trioxide and molten potassium normal sulfate to solvate the sulfur trioxide to remove the sulfur trioxide from the gaseous stream. A portion of the sulfur trioxide loaded salt mixture is then dissociated to produce sulfur trioxide gas and thereby regenerate potassium normal sulfate. The evolved sulfur trioxide is reacted with hydrogen sulfide as in a Claus reactor to produce elemental sulfur. The process may be advantageously used to clean waste stack gas from industrial plants, such as copper smelters, where a supply of hydrogen sulfide is readily available.

Moore, Raymond H. (Richland, WA)

1977-01-01T23:59:59.000Z

12

Biological trace element measurements using synchrotron radiation  

SciTech Connect

The feasibility of performing x-ray fluorescence trace element determinations at concentrations substantially below the ppM level for biological materials is demonstrated. Conditions for achieving optimum sensitivity were ascertained. Results achieved for five standard reference materials were, in most cases, in excellent agreement with listed values. Minimum detectable limits of 20 ppM were measured for most elements.

Giauque, R.D.; Jaklevic, J.M.; Thompson, A.C.

1985-07-01T23:59:59.000Z

13

Trace elements in oil shale. Progress report, 1976--1979  

DOE Green Energy (OSTI)

The overall objective of the program is to evaluate the environmental and health consequences of the release of toxic trace elements (As, B, F, Mo, Se) by shale oil production and use. Some of the particularly significant results are: The baseline geochemical survey shows that stable trace elements maps can be constructed for numerous elements and that the trends observed are related to geologic and climatic factors. Shale retorted by above-ground processes tends to be very homogeneous (both in space and in time) in trace element content. This implies that the number of analytical determinations required of processed shales is not large. Leachate studies show that significant amounts of B, F, And Mo are released from retorted shales and while B and Mo are rapidly flushed out, F is not. On the other hand, As, Se, and most other trace elements ae not present in significant quantities. Significant amounts of F and B are also found in leachates of raw shales. Very large concentrations of reduced sulfur species are found in leachates of processed shale. Upon oxidation a drastic lowering in pH is observed. Preliminary data indicates that this oxidation is catalyzed by bacteria. Very high levels of B and Mo are taken up in some plants growing on processed shale with and without soil cover. These amounts depend upon the process and various site specific characteristics. In general, the amounts taken up decrease with increasing soil cover. On the other hand, we have not observed significant uptake of As, Se, and F into plants. There is a tendency for some trace elements to associate with specific organic fractions, indicating that organic chelation or complexation may play an important role. In particular, most of the Cd, Se, and Cr in shale oil is associated with the organic fraction containing most of the nitrogen-containing compounds.

Chappell, W.R.

1979-01-01T23:59:59.000Z

14

12.479 Trace-Element Geochemistry, Fall 2006  

E-Print Network (OSTI)

Focuses on element distribution in rocks and minerals using data obtained from natural and experimental systems. Emphasizes models describing trace-element partitioning and applications of trace-element geochemistry to ...

Frey, Frederick August

15

Trace element speciation under coal fired power station conditions  

Science Conference Proceedings (OSTI)

Coal combustion from power stations is one of the largest contributors of potentially toxic trace elements to the environment. Some trace elements may be released in range of valencies, often with varying toxicity and bioavailability. Hence, determination ... Keywords: arsenic, chromium, coal combustion, mercury, selenium, speciation, trace elements

Pushan Shah; Vladimir Strezov; Peter F. Nelson

2007-05-01T23:59:59.000Z

16

Leaching of Trace Elements From Highway Materials Stabilized ...  

Leaching of Trace Elements From Highway Materials Stabilized with Coal Fly Ash Craig H. Benson, PhD, PE Professor, Geo Engineering Program Dept. of ...

17

KINETICS OF DIRECT OXIDATION OF H2S IN COAL GAS TO ELEMENTAL SULFUR  

DOE Green Energy (OSTI)

The direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and the hot-gas desulfurization using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process. The objective of this research is to support the near- and long-term process development efforts to commercialize this direct oxidation technology. The objectives of this research are to measure kinetics of direct oxidation of H{sub 2}S to elemental sulfur in the presence of a simulated coal gas mixture containing SO{sub 2}, H{sub 2}, and moisture, using 160-{micro}m C-500-04 alumina catalyst particles and a micro bubble reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. To achieve the above-mentioned objectives, experiments on conversion of hydrogen sulfide into liquid elemental sulfur were carried out for the space time range of 1-6 milliseconds at 125-155 C to evaluate effects of reaction temperature, moisture concentration, reaction pressure on conversion of hydrogen sulfide into liquid elemental sulfur. Simulated coal gas mixtures consist of 70 v% hydrogen, 2,500-7,500-ppmv hydrogen sulfide, 1,250-3,750 ppmv sulfur dioxide, and 0-15 vol% moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to a micro bubble reactor are 100 cm{sup 3}/min at room temperature and atmospheric pressure. The temperature of the reactor is controlled in an oven at 125-155 C. The pressure of the reactor is maintained at 40-170 psia.

K.C. Kwon

2004-01-01T23:59:59.000Z

18

KINETICS OF DIRECT OXIDATION OF H2S IN COAL GAS TO ELEMENTAL SULFUR  

DOE Green Energy (OSTI)

The direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and the hot-gas desulfurization using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process. The objective of this research is to support the near- and long-term process development efforts to commercialize this direct oxidation technology. The objectives of this research are to measure kinetics of direct oxidation of H{sub 2}S to elemental sulfur in the presence of a simulated coal gas mixture containing SO{sub 2}, H{sub 2}, and moisture, using 160-{micro}m C-500-04 alumina catalyst particles and a micro bubble reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. To achieve the above-mentioned objectives, experiments on conversion of hydrogen sulfide into liquid elemental sulfur were carried out for the space time range of 0.059-0.87 seconds at 125-155 C to evaluate effects of reaction temperature, H{sub 2}S concentration, reaction pressure, and catalyst loading on conversion of hydrogen sulfide into liquid elemental sulfur. Simulated coal gas mixtures consist of 62-78 v% hydrogen, 3,000-7,000-ppmv hydrogen sulfide, 1,500-3,500 ppmv sulfur dioxide, and 10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to a micro bubble reactor are 50 cm{sup 3}/min at room temperature and atmospheric pressure. The temperature of the reactor is controlled in an oven at 125-155 C. The pressure of the reactor is maintained at 40-170 psia. The molar ratio of H{sub 2}S to SO{sub 2} in the bubble reactor is maintained at 2 for all the reaction experiment runs.

K.C. Kwon

2005-01-01T23:59:59.000Z

19

Effect of Trace Elements on Anaerobic Digestion of Coking Wastewater  

Science Conference Proceedings (OSTI)

The pretreatment of coking wastewater using ASBR was conducted at 35? in this paper. The addition of trace elements to the anaerobic reactor has positive effect on the anaerobic treatment of coking wastewater, but too much or too little of it will ... Keywords: trace elements, anaerobic digestion, coking wastewater

Yu-ying Li; Bing Li

2009-10-01T23:59:59.000Z

20

Kinetics of Direct Oxidation of H2S in Coal Gas to Elemental Sulfur  

SciTech Connect

Removal of hydrogen sulfide (H{sub 2}S) from coal gasifier gas and sulfur recovery are key steps in the development of Department of Energy's (DOE's) advanced Vision 21 plants that produce electric power and clean transportation fuels with coal and natural gas. These Vision 21 plants will require highly clean coal gas with H{sub 2}S below 1 ppm and negligible amounts of trace contaminants such as hydrogen chloride, ammonia, alkali, heavy metals, and particulate. The conventional method of sulfur removal and recovery employing amine, Claus, and tail-gas treatment is very expensive. A second generation approach developed under DOE's sponsorship employs hot-gas desulfurization (HGD) using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process (DSRP). However, this process sequence does not remove trace contaminants and is targeted primarily towards the development of advanced integrated gasification combined cycle (IGCC) plants that produce electricity (not both electricity and transportation fuels). There is an immediate as well as long-term need for the development of cleanup processes that produce highly clean coal gas for next generation Vision 21 plants. To this end, a novel process is now under development at several research organizations in which the H{sub 2}S in coal gas is directly oxidized to elemental sulfur over a selective catalyst. Such a process is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. The direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and HGD/DSRP. The objectives of this research are to measure kinetics of direct oxidation of H{sub 2}S to elemental sulfur in the presence of a simulated coal gas mixture containing SO{sub 2}, H{sub 2}, and moisture, using 160-{micro}m C-500-04 alumina catalyst particles and 400 square cells/inch{sup 2}, {gamma}-Al{sub 2}O{sub 3}-wash-coated monolithic catalyst, and various reactors such as a micro packed-bed reactor, a micro bubble reactor, and a monolithic catalyst reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam.

K.C. Kwon

2005-11-01T23:59:59.000Z

Note: This page contains sample records for the topic "trace elements 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

Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts  

DOE Green Energy (OSTI)

Removal of hydrogen sulfide (H{sub 2}S) from coal gasifier gas and sulfur recovery are key steps in the development of Department of Energy's (DOE's) advanced power plants that produce electric power and clean transportation fuels with coal and natural gas. These plants will require highly clean coal gas with H{sub 2}S below 1 ppmv and negligible amounts of trace contaminants such as hydrogen chloride, ammonia, alkali, heavy metals, and particulate. The conventional method of sulfur removal and recovery employing amine, Claus, and tail-gas treatment is very expensive. A second generation approach developed under DOE's sponsorship employs hot-gas desulfurization (HGD) using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process (DSRP). However, this process sequence does not remove trace contaminants and is targeted primarily towards the development of advanced integrated gasification combined cycle (IGCC) plants that produce electricity (not both electricity and transportation fuels). There is an immediate as well as long-term need for the development of cleanup processes that produce highly clean coal gas for next generation power plants. To this end, a novel process is now under development at several research organizations in which the H{sub 2} in coal gas is directly oxidized to elemental sulfur over a selective catalyst. Such a process is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S In the Single-Step Sulfur Recovery Process (SSRP), the direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and HGD/DSRP. The H{sub 2} and CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash or carbon coats, and catalytic metals, to develop a catalytic regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. To achieve the above-mentioned objectives using a monolithic catalyst reactor, experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 40-560 seconds at 120-150 C to evaluate effects of reaction temperatures, total pressure, space time, and catalyst regeneration on conversion of hydrogen sulfide into elemental sulfur and formation of COS. Simulated coal gas mixtures consist of 3,600-4,000-ppmv hydrogen sulfide, 1,800-2,000 ppmv sulfur dioxide, 23-27 v% hydrogen, 36-41 v% CO, 10-12 v% CO{sub 2}, 0-10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to the reactor are 30-180 SCCM. The temperature of the reactor is controlled in an oven at 120-150 C. The pressure of the reactor is maintained at 40-210 psia. The molar ratio of H{sub 2}S to SO{sub 2} in the monolithic catalyst reactor is mai

K. C. Kwon

2006-09-30T23:59:59.000Z

22

Factors influencing trace element composition in human teeth  

SciTech Connect

The authors recently compiled and reviewed the literature published in or after 1978 for 45 major, minor, and trace elements in human teeth as a part of an International Atomic Energy Agency (IAEA) study. The purpose of this paper is to discuss the various factors that influence the concentration levels of certain trace elements in human teeth. The sampling practices and analytical techniques that are applicable for trace element analysis are also discussed. It is also our intention to identify reference range of values, where data permit such conclusions. The scrutiny was designed to identify only the healthy permanent teeth, and values from teeth with fillings, caries, or periodontal diseases were eliminated.

Tandon, L. [Los Alamos National Lab., NM (United States); Iyengar, G.V. [Biomineral Sciences International, Inc., Bethesda, MD (United States)

1997-12-01T23:59:59.000Z

23

Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts  

DOE Green Energy (OSTI)

Removal of hydrogen sulfide (H{sub 2}S) from coal gasifier gas and sulfur recovery are key steps in the development of Department of Energy's (DOE's) advanced power plants that produce electric power and clean transportation fuels with coal and natural gas. These plants will require highly clean coal gas with H{sub 2}S below 1 ppmv and negligible amounts of trace contaminants such as hydrogen chloride, ammonia, alkali, heavy metals, and particulate. The conventional method of sulfur removal and recovery employing amine, Claus, and tail-gas treatment is very expensive. A second generation approach developed under DOE's sponsorship employs hot-gas desulfurization (HGD) using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process (DSRP). However, this process sequence does not remove trace contaminants and is targeted primarily towards the development of advanced integrated gasification combined cycle (IGCC) plants that produce electricity (not both electricity and transportation fuels). There is an immediate as well as long-term need for the development of cleanup processes that produce highly clean coal gas for next generation power plants. To this end, a novel process is now under development at several research organizations in which the H{sub 2}S in coal gas is directly oxidized to elemental sulfur over a selective catalyst. Such a process is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S In the Single-Step Sulfur Recovery Process (SSRP), the direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and HGD/DSRP. The H{sub 2} and CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash or carbon coats, and catalytic metals, to develop a catalytic regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. Experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 130-156 seconds at 120-140 C to formulate catalysts suitable for the removal of H{sub 2}S and COS from coal gases, evaluate removal capabilities of hydrogen sulfide and COS from coal gases with formulated catalysts, and develop an economic regeneration method of deactivated catalysts. Simulated coal gas mixtures consist of 3,300-3,800-ppmv hydrogen sulfide, 1,600-1,900 ppmv sulfur dioxide, 18-21 v% hydrogen, 29-34 v% CO, 8-10 v% CO{sub 2}, 5-18 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to the reactor are 114-132 SCCM. The temperature of the reactor is controlled in an oven at 120-140 C. The pressure of the reactor is maintained at 116-129 psia. The molar ratio of H{sub 2}S to SO{sub 2} in the monolithic catalyst reactor is

K. C. Kwon

2007-09-30T23:59:59.000Z

24

Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts  

DOE Green Energy (OSTI)

Removal of hydrogen sulfide (H{sub 2}S) from coal gasifier gas and sulfur recovery are key steps in the development of Department of Energy's (DOE's) advanced power plants that produce electric power and clean transportation fuels with coal and natural gas. These plants will require highly clean coal gas with H{sub 2}S below 1 ppmv and negligible amounts of trace contaminants such as hydrogen chloride, ammonia, alkali, heavy metals, and particulate. The conventional method of sulfur removal and recovery employing amine, Claus, and tail-gas treatment is very expensive. A second generation approach developed under DOE's sponsorship employs hot-gas desulfurization (HGD) using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process (DSRP). However, this process sequence does not remove trace contaminants and is targeted primarily towards the development of advanced integrated gasification combined cycle (IGCC) plants that produce electricity (not both electricity and transportation fuels). There is an immediate as well as long-term need for the development of cleanup processes that produce highly clean coal gas for next generation power plants. To this end, a novel process is now under development at several research organizations in which the H{sub 2}S in coal gas is directly oxidized to elemental sulfur over a selective catalyst. Such a process is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S In the Single-Step Sulfur Recovery Process (SSRP), the direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and HGD/DSRP. The H{sub 2} and CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash coat, and catalytic metals, to develop a regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor. The task of developing kinetic rate equations and modeling the direct oxidation process to assist in the design of large-scale plants will be abandoned since formulation of catalysts suitable for the removal of H{sub 2}S and COS is being in progress. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. Experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 46-570 seconds under reaction conditions to formulate catalysts suitable for the removal of H{sub 2}S and COS from coal gases and evaluate their capabilities in reducing hydrogen sulfide and COS in coal gases. Simulated coal gas mixtures consist of 3,200-4,000-ppmv hydrogen sulfide, 1,600-20,000-ppmv sulfur dioxide, 18-27 v% hydrogen, 29-41 v% CO, 8-12 v% CO{sub 2}, 0-10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of simulated coal gas mixtures to the reactor are 30 - 180 cm{sup 3}/min at 1 atm and 25 C (SCCM). The temperature of the reactor is controlled in an oven at 120-155 C. The pressure of the reactor is maintained at 40-210 psia. The molar ratio

K.C. Kwon

2009-09-30T23:59:59.000Z

25

Selective catalytic reduction of sulfur dioxide to elemental sulfur. Final report  

Science Conference Proceedings (OSTI)

This project has investigated new metal oxide catalysts for the single stage selective reduction of SO{sub 2} to elemental sulfur by a reductant, such as CO. Significant progress in catalyst development has been made during the course of the project. We have found that fluorite oxides, CeO{sub 2} and ZrO{sub 2}, and rare earth zirconates such as Gd{sub 2}Zr{sub 2}O{sub 7} are active and stable catalysts for reduction Of SO{sub 2} by CO. More than 95% sulfur yield was achieved at reaction temperatures about 450{degrees}C or higher with the feed gas of stoichiometric composition. Reaction of SO{sub 2} and CO over these catalysts demonstrated a strong correlation of catalytic activity with the catalyst oxygen mobility. Furthermore, the catalytic activity and resistance to H{sub 2}O and CO{sub 2} poisoning of these catalysts were significantly enhanced by adding small amounts of transition metals, such as Co, Ni, Co, etc. The resulting transition metal-fluorite oxide composite catalyst has superior activity and stability, and shows promise in long use for the development of a greatly simplified single-step sulfur recovery process to treat variable and dilute SO{sub 2} concentration gas streams. Among various active composite catalyst systems the Cu-CeO{sub 2} system has been extensively studied. XRD, XPS, and STEM analyses of the used Cu-CeO{sub 2} catalyst found that the fluorite crystal structure of ceria was stable at the present reaction conditions, small amounts of copper was dispersed and stabilized on the ceria matrix, and excess copper oxide particles formed copper sulfide crystals of little contribution to catalytic activity. A working catalyst consisted of partially sulfated cerium oxide surface and partially sulfided copper clusters. The overall reaction kinetics were approximately represented by a first order equation.

Liu, W.; Flytzani-Stephanopoulos, M.; Sarofim, A.F.

1995-06-01T23:59:59.000Z

26

Trace element fingerprinting of ancient Chinese gold with femtosecond laser  

NLE Websites -- All DOE Office Websites (Extended Search)

Trace element fingerprinting of ancient Chinese gold with femtosecond laser Trace element fingerprinting of ancient Chinese gold with femtosecond laser ablation-inductivity coupled mass spectrometry Title Trace element fingerprinting of ancient Chinese gold with femtosecond laser ablation-inductivity coupled mass spectrometry Publication Type Journal Article Year of Publication 2009 Authors Brostoff, Lynn B., Jhanis J. Gonzalez, Paul Jett, and Richard E. Russo Journal Journal of Archeological Science Volume 36 Start Page 461 Issue 2 Pagination 461-466 Date Published 02/2009 Keywords Ancient gold, femtosecond, la-icp-ms, Trace element Abstract In this collaborative investigation, femtosecond laser ablation-inductively coupled mass spectrometry (LA-ICP-MS) was applied to the study of a remarkable group of ancient Chinese gold objects in the Smithsonian's Freer Gallery of Art and Arthur M. Sackler Gallery. Taking advantage of the superior ablation characteristics and high precision of a femtosecond 266 nm Ti:sapphire laser at Lawrence Berkeley National Laboratory, major, minor and trace element concentrations in the gold fragments were quantified. Results validate use of femtosecond LA-ICP-MS for revealing ''fingerprints'' in minute gold samples. These fingerprints allow us to establish patterns based on the association of silver, palladium and platinum that support historical, technical and stylistic relationships, and shed new light on these ancient objects.

27

Sulfur polymer cement stabilization of elemental mercury mixed waste  

SciTech Connect

Elemental mercury, contaminated with radionuclides, is a problem throughout the Department of Energy (DOE) complex. This report describes the development and testing of a process to immobilize elemental mercury, contaminated with radionuclides, in a form that is non-dispersible, will meet EPA leaching criteria, and has low mercury vapor pressure. In this stabilization and solidification process (patent pending) elemental mercury is mixed with an excess of powdered sulfur polymer cement (SPC) and additives in a vessel and heated to {approximately}35 C, for several hours, until all of the mercury is converted into mercuric sulfide (HgS). Additional SPC is then added and the mixture raised to 135 C, resulting in a homogeneous molten liquid which is poured into a suitable mold where is cools and solidifies. The final stabilized and solidified waste forms were characterized by powder X-ray diffraction, as well as tested for leaching behavior and mercury vapor pressure. During this study the authors have processed the entire inventory of mixed mercury waste stored at Brookhaven National Laboratory (BNL).

Melamed, D.; Fuhrmann, M.; Kalb, P.; Patel, B.

1998-04-01T23:59:59.000Z

28

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

NLE Websites -- All DOE Office Websites (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

29

Concentration of major and trace elements in the Miocene lignite from the Canakkale-Can coalfield  

SciTech Connect

This study focuses on major and trace element concentrations of three lignite samples, of which two are from the working lignite seam and one from a feed coal to an thermal power plant. The Canakkale-Can lignite deposit is currently being mined by open-cast mining methods despite its high sulfur content. The production lignites are mainly consumed by a fluidized-bed thermal power plant with 2 160 MW capacity and less domestic heating and industrial factories around Can. Major oxide compositions of the coal ash samples imply that the more abundant oxides are SiO{sub 2} and Al{sub 2}O{sub 3} and less CaO and Fe2O{sub 3}. Trace element concentrations in the samples on whole-coal basis show that three samples analyzed were enriched in V, and also concentrations of B, Sc, Sn, Th, Tl, and U in one sample that exceed the range values of most world coals.

Inaner, H.; Karayigit, A. [Dokuz Eylul University, Izmir (Turkey). Dept. of Geological Engineering

2008-07-01T23:59:59.000Z

30

AIR QUALITY: MERCURY, TRACE ELEMENTS, AND PARTICULATE MATTER CONFERENCE  

SciTech Connect

This final report summarizes the planning/preparation, facilitation, and outcome of the conference entitled ''Air Quality: Mercury, Trace Elements, and Particulate Matter'' that was held December 1-4, 1998, in McLean, Virginia (on the outskirts of Washington, DC). The goal of the conference was to bring together industry, government, and the research community to discuss the critical issue of how air quality can impact human health and the ecosystem, specifically hazardous air pollutants and fine airborne particles; available and developing control technologies; strategies and research needs; and an update on federal and state policy and regulations, related implementation issues, and the framework of the future.

John H. Pavlish; Steven A. Benson

1999-07-01T23:59:59.000Z

31

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

E-Print Network (OSTI)

efficiency by sulfur and/or chlorine containing compounds atfired Flue Gas by Sulfur-chlorine Compounds Nai-Qiang Yanremoval. Two sulfur-chlorine compounds, sulfur dichloride (

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

2008-01-01T23:59:59.000Z

32

Adsorption of Trace Elements on Fresh and Weathered Coal Fly Ash  

Science Conference Proceedings (OSTI)

A variety of trace elements are associated with fly ash produced by coal combustion. These trace elements are potentially of concern for human health if they are released to the environment, and thus it is important to understand their mobility in coal fly ash management settings. In the fly ash management environment, the ash may react with meteoric fluid to release trace elements into groundwater or surface water. However, fly ash particles also have a relatively high surface area and have the ability ...

2012-05-23T23:59:59.000Z

33

Process and apparatus for generating elemental sulfur and re-usable metal oxide from spent metal sulfide sorbents  

DOE Patents (OSTI)

A process and apparatus for generating elemental sulfur and re-usable metal oxide from spent metal-sulfur compound. Spent metal-sulfur compound is regenerated to re-usable metal oxide by moving a bed of spent metal-sulfur compound progressively through a single regeneration vessel having a first and second regeneration stage and a third cooling and purging stage. The regeneration is carried out and elemental sulfur is generated in the first stage by introducing a first gas of sulfur dioxide which contains oxygen at a concentration less than the stoichiometric amount required for complete oxidation of the spent metal-sulfur compound. A second gas containing sulfur dioxide and excess oxygen at a concentration sufficient for complete oxidation of the partially spent metal-sulfur compound, is introduced into the second regeneration stage. Gaseous sulfur formed in the first regeneration stage is removed prior to introducing the second gas into the second regeneration stage. An oxygen-containing gas is introduced into the third cooling and purging stage. Except for the gaseous sulfur removed from the first stage, the combined gases derived from the regeneration stages which are generally rich in sulfur dioxide and lean in oxygen, are removed from the regenerator as an off-gas and recycled as the first and second gas into the regenerator. Oxygen concentration is controlled by adding air, oxygen-enriched air or pure oxygen to the recycled off-gas.

Ayala, Raul E. (Clifton Park, NY); Gal, Eli (Lititz, PA)

1995-01-01T23:59:59.000Z

34

Trace Element Remediation by Free-Living and Plant-Associated Microbes  

Science Conference Proceedings (OSTI)

Plants can accumulate, detoxify, and transform trace elements present in contaminated soil and water, leading to the phytoremediation of contaminated sites. This study considers the role of plant-associated microbes in the phytoremediation of trace elements, particularly selenium (Se), in the root zone (rhizosphere) as well as the isolation and characterization of free-living microbes for Se bioremediation.

2003-11-05T23:59:59.000Z

35

Elevated Trace Element Concentrations in Southern Toads, Bufo terrestris, Exposed to Coal Combustion Waste  

E-Print Network (OSTI)

Elevated Trace Element Concentrations in Southern Toads, Bufo terrestris, Exposed to Coal, and behavioral abnormalities in amphibians to coal combustion wastes (coal ash). Few studies, however, have determined trace element concentrations in amphibians exposed to coal ash. In the current study we compare

Hopkins, William A.

36

Laboratory Evaluation of Novel Trace Element Removal Technologies for Wet FGD Wastewater  

Science Conference Proceedings (OSTI)

Wet flue gas desulfurization (FGD) systems can remove a wide range of trace elements, such as mercury, selenium, arsenic, and others from the flue gas. Some trace elements leave the FGD system with solid byproduct streams, but a portion generally leaves as dissolved species in the FGD chloride purge stream. The U.S. Environmental Protection Agency (EPA) effluent limitation guidelines and state or local regulations generally limit the quantities of these trace species in wastewater discharges from ...

2012-12-31T23:59:59.000Z

37

Trace Element Analysis At Walker-Lane Transitional Zone Region (Coolbaugh,  

Open Energy Info (EERE)

Trace Element Analysis At Walker-Lane Transitional Zone Region (Coolbaugh, Trace Element Analysis At Walker-Lane Transitional Zone Region (Coolbaugh, Et Al., 2010) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Trace Element Analysis At Walker-Lane Transitional Zone Region (Coolbaugh, Et Al., 2010) Exploration Activity Details Location Walker-Lane Transition Zone Geothermal Region Exploration Technique Trace Element Analysis Activity Date Usefulness useful DOE-funding Unknown Notes "This second paper provides more detailed documentation on water and rock geochemistries and describes diagnostic major and trace element ratios and concentrations that can be used to distinguish tufa columns formed from thermal waters from those that formed from non-thermal waters." "In addition to providing a potentially diagnostic lithogeochemical tool for

38

Trace Element Analysis At Nw Basin & Range Region (Coolbaugh, Et Al., 2010)  

Open Energy Info (EERE)

Trace Element Analysis At Nw Basin & Range Region (Coolbaugh, Et Al., 2010) Trace Element Analysis At Nw Basin & Range Region (Coolbaugh, Et Al., 2010) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Trace Element Analysis At Nw Basin & Range Region (Coolbaugh, Et Al., 2010) Exploration Activity Details Location Northwest Basin and Range Geothermal Region Exploration Technique Trace Element Analysis Activity Date Usefulness useful DOE-funding Unknown Notes "This second paper provides more detailed documentation on water and rock geochemistries and describes diagnostic major and trace element ratios and concentrations that can be used to distinguish tufa columns formed from thermal waters from those that formed from non-thermal waters." "In addition to providing a potentially diagnostic lithogeochemical tool for

39

Selective Catalytic Oxidation of Hydrogen Sulfide to Elemental Sulfur from Coal-Derived Fuel Gases  

SciTech Connect

The development of low cost, highly efficient, desulfurization technology with integrated sulfur recovery remains a principle barrier issue for Vision 21 integrated gasification combined cycle (IGCC) power generation plants. In this plan, the U. S. Department of Energy will construct ultra-clean, modular, co-production IGCC power plants each with chemical products tailored to meet the demands of specific regional markets. The catalysts employed in these co-production modules, for example water-gas-shift and Fischer-Tropsch catalysts, are readily poisoned by hydrogen sulfide (H{sub 2}S), a sulfur contaminant, present in the coal-derived fuel gases. To prevent poisoning of these catalysts, the removal of H{sub 2}S down to the parts-per-billion level is necessary. Historically, research into the purification of coal-derived fuel gases has focused on dry technologies that offer the prospect of higher combined cycle efficiencies as well as improved thermal integration with co-production modules. Primarily, these concepts rely on a highly selective process separation step to remove low concentrations of H{sub 2}S present in the fuel gases and produce a concentrated stream of sulfur bearing effluent. This effluent must then undergo further processing to be converted to its final form, usually elemental sulfur. Ultimately, desulfurization of coal-derived fuel gases may cost as much as 15% of the total fixed capital investment (Chen et al., 1992). It is, therefore, desirable to develop new technology that can accomplish H{sub 2}S separation and direct conversion to elemental sulfur more efficiently and with a lower initial fixed capital investment.

Gardner, Todd H.; Berry, David A.; Lyons, K. David; Beer, Stephen K.; Monahan, Michael J.

2001-11-06T23:59:59.000Z

40

Comparative assessment of the trace-element composition of coals, crude oils, and oil shales  

Science Conference Proceedings (OSTI)

A comparative analysis of the amounts of 42 trace elements in coals, crude oils, and oil and black shales was performed. The degree of concentration of trace elements by caustobioliths and their ashes relative to their abundance in argillaceous rocks and the Earth's crust was calculated. Typomorphic trace elements were distinguished, of which many turned out to be common for the different kinds of caustobioliths in question. The trace elements were classified according to their concentration factors in different caustobioliths. The ash of crude oils is enriched in trace elements (Cs, V, Mo, Cu, Ag, Au, Zn, Hg, Se, Cr, Co, Ni, U) to the greatest extent (concentration factor above 3.5) and that of oil shales is enriched to the least extent (Re, Cs, Hg, Se). The ratios between typomorphic trace elements in general strongly differ from those in the Earth's crust and argillaceous rocks and are not identical in different caustobioliths. Quantitative parameters that make it possible to calculate a change in these ratios on passing from one caustobiolith type to another were proposed and the relative trace-element affinity of different caustobioliths was estimated.

M.Y. Shpirt; S.A. Punanova [Institute for Fossil Fuels, Moscow (Russian Federation)

2007-10-15T23:59:59.000Z

Note: This page contains sample records for the topic "trace elements 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

JV Task-123 Determination of Trace Element Concentrations at an Eastern Bituminous Coal Plant Employing an SCR and Wet FGD  

SciTech Connect

The Energy & Environmental Research Center (EERC), in partnership with Babcock & Wilcox (B&W) and with funding from U.S. Department of Energy (DOE), conducting tests to prove that a high level of mercury control (>90%) can be achieved at a power plant burning a high-sulfur eastern bituminous coal. With funding from the Electric Power Research Institute (EPRI), DOE, and Center for Air Toxic Metals{reg_sign} (CATM{reg_sign}) Affiliates Program, the EERC completed an additional sampling project to provide data as to the behavior of a number of trace elements across the various pollution control devices, with a special emphasis on the wet flue gas desulfurization (FGD) system. Results showed that the concentrations of almost all the elements of interest leaving the stack were very low, and a high percentage of the trace elements were captured in the electrostatic precipitator (ESP) (for most, >80%). Although, with a few exceptions, the overall mass balances were generally quite good, the mass balances across the wet FGD were more variable. This is most likely a result of some of the concentrations being very low and also the uncertainties in determining flows within a wet FGD.

Dennis Laudal

2008-05-01T23:59:59.000Z

42

Trace-Element Distribution In An Active Hydrothermal System, Roosevelt Hot  

Open Energy Info (EERE)

Trace-Element Distribution In An Active Hydrothermal System, Roosevelt Hot Trace-Element Distribution In An Active Hydrothermal System, Roosevelt Hot Springs Thermal Area, Utah Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Journal Article: Trace-Element Distribution In An Active Hydrothermal System, Roosevelt Hot Springs Thermal Area, Utah Details Activities (3) Areas (1) Regions (0) Abstract: Chemical interaction of thermal fluids with reservoir rock in the Roosevelt Hot Springs thermal area, Utah, has resulted in the development of characteristic trace-element dispersion patterns. Multielement analyses of surface rock samples, soil samples and drill cuttings from deep exploration wells provide a three-dimensional perspective of chemical redistribution within this structurally-controlled hot-water geothermal system. Five distinctive elemental suites of chemical enrichment are

43

Trace Element Analysis At Socorro Mountain Area (Owens, Et Al., 2005) |  

Open Energy Info (EERE)

Trace Element Analysis At Socorro Mountain Area (Owens, Et Al., 2005) Trace Element Analysis At Socorro Mountain Area (Owens, Et Al., 2005) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Trace Element Analysis At Socorro Mountain Area (Owens, Et Al., 2005) Exploration Activity Details Location Socorro Mountain Area Exploration Technique Trace Element Analysis Activity Date Usefulness not indicated DOE-funding Unknown Notes In order to determine which of the faults in these regions were active and open to hydrothermal fluid circulation, we have employed selective ion geochemistry that is a new geochemical method capable of detecting anomalous concentrations for up to 47 elements transported to soils by geochemical cells or low pressure vapors. Enzyme leach and Terrasol leach are two such techniques. This method has to datae been mostly applied to

44

Trace Element Geochemical Zoning in the Roosevelt Hot Springs Thermal Area,  

Open Energy Info (EERE)

Page Page Edit with form History Facebook icon Twitter icon » Trace Element Geochemical Zoning in the Roosevelt Hot Springs Thermal Area, Utah Jump to: navigation, search OpenEI Reference LibraryAdd to library Conference Paper: Trace Element Geochemical Zoning in the Roosevelt Hot Springs Thermal Area, Utah Abstract Chemical interaction of thermal brines with reservoir rock in the Roosevelt Hot Springs thermal area has resulted in the development of distinctive trace element signatures. Geochemical analysis of soil sample, shallow temperature gradient drill hole cuttings and deep drill hole cutting provides a three dimensional perspective of trace element distributions within the system. Distributions of As, Hg and Li provide the clearest expression of hydrothermal activity. Comparison of these distribution

45

Theoretical investigation of selected trace elements in coal gasification plants. Final report Mar 78-Nov 79  

SciTech Connect

The report gives results of a theoretical investigation of the disposition of five volatile trace elements (arsenic, boron, lead, selenium, and mercury) in SNG-producing coal gasification plants. Three coal gasification processes (dry-bottom Lurgi, Koppers-Totzek, and HYGAS) were investigated to examine the possible effects of gasifier operation conditions on the speciation of the volatile trace elements. Results of this investigation suggest that none of the trace elements considered in this study will be present in the product SNG from a coal gasification plant, but will be removed from the fuel gas by various unit operations. Results also suggest that speciation of these volatile trace elements is not significantly affected by gasifier conditions.

Hill, A.H.; Anderson, G.L.; Fleming, D.K.

1983-08-01T23:59:59.000Z

46

Long-term anaerobic digestion of food waste stabilized by trace elements  

SciTech Connect

Highlights: Black-Right-Pointing-Pointer Korean food waste was found to contain low level of trace elements. Black-Right-Pointing-Pointer Stable anaerobic digestion of food waste was achieved by adding trace elements. Black-Right-Pointing-Pointer Iron played an important role in anaerobic digestion of food waste. Black-Right-Pointing-Pointer Cobalt addition further enhanced the process performance in the presence of iron. - Abstract: The purpose of this study was to examine if long-term anaerobic digestion of food waste in a semi-continuous single-stage reactor could be stabilized by supplementing trace elements. Contrary to the failure of anaerobic digestion of food waste alone, stable anaerobic digestion of food waste was achieved for 368 days by supplementing trace elements. Under the conditions of OLR (organic loading rates) of 2.19-6.64 g VS (volatile solid)/L day and 20-30 days of HRT (hydraulic retention time), a high methane yield (352-450 mL CH{sub 4}/g VS{sub added}) was obtained, and no significant accumulation of volatile fatty acids was observed. The subsequent investigation on effects of individual trace elements (Co, Fe, Mo and Ni) showed that iron was essential for maintaining stable methane production. These results proved that the food waste used in this study was deficient in trace elements.

Zhang Lei, E-mail: wxzyfx@yahoo.com [Key Laboratory of Industrial Ecology and Environmental Engineering, School of Environmental Science and Technology, Dalian University of Technology, Linggong Road 2, Dalian 116024 (China); Jahng, Deokjin, E-mail: djahng@mju.ac.kr [Department of Environmental Engineering and Biotechnology, Myongji University, San 38-2, Namdong, Cheoin-Gu, Yongin, Gyeonggi-Do 449-728 (Korea, Republic of)

2012-08-15T23:59:59.000Z

47

Trace Element Geochemical Zoning in the Roosevelt Hot Springs...  

Open Energy Info (EERE)

Element Geochemical Zoning in the Roosevelt Hot Springs Thermal Area, Utah Abstract Chemical interaction of thermal brines with reservoir rock in the Roosevelt Hot Springs...

48

Trace Element Analysis At Walker-Lane Transitional Zone Region...  

Open Energy Info (EERE)

the analysis of lithium and other elements in tufa deposits could serve as exploration guides for hot spring lithium deposits." References Mark Coolbaugh, Paul Lechler, Chris...

49

Trace Element Analysis At Northern Basin & Range Region (Coolbaugh...  

Open Energy Info (EERE)

the analysis of lithium and other elements in tufa deposits could serve as exploration guides for hot spring lithium deposits." References Mark Coolbaugh, Paul Lechler, Chris...

50

Trace Element Analysis At Central Nevada Seismic Zone Region...  

Open Energy Info (EERE)

the analysis of lithium and other elements in tufa deposits could serve as exploration guides for hot spring lithium deposits." References Mark Coolbaugh, Paul Lechler, Chris...

51

Trace Element Analysis At Nw Basin & Range Region (Coolbaugh...  

Open Energy Info (EERE)

the analysis of lithium and other elements in tufa deposits could serve as exploration guides for hot spring lithium deposits." References Mark Coolbaugh, Paul Lechler, Chris...

52

Trace Element Analysis At Central Nevada Seismic Zone Region (Coolbaugh, Et  

Open Energy Info (EERE)

Coolbaugh, Et Coolbaugh, Et Al., 2010) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Trace Element Analysis At Central Nevada Seismic Zone Region (Coolbaugh, Et Al., 2010) Exploration Activity Details Location Central Nevada Seismic Zone Geothermal Region Exploration Technique Trace Element Analysis Activity Date Usefulness useful DOE-funding Unknown Notes "This second paper provides more detailed documentation on water and rock geochemistries and describes diagnostic major and trace element ratios and concentrations that can be used to distinguish tufa columns formed from thermal waters from those that formed from non-thermal waters." "In addition to providing a potentially diagnostic lithogeochemical tool for geothermal exploration, the analysis of lithium and other elements in tufa

53

Trace-element geochemistry of coal resource development related to environmental quality and health  

Science Conference Proceedings (OSTI)

This report assesses for decision makers and those involved in coal resource development the environmental and health impacts of trace-element effects arising from significant increases in the use of coal, unless unusual precautions are invoked. Increasing demands for energy and the pressing need for decreased dependence of the United States on imported oil require greater use of coal to meet the nation's energy needs during the next decade. If coal production and consumption are increased at a greatly accelerated rate, concern arises over the release, mobilization, transportation, distribution, and assimilation of certain trace elements, with possible adverse effects on the environment and human health. It is, therefore, important to understand their geochemical pathways from coal and rocks via air, water, and soil to plants, animals, and ultimately humans, and their relation to health and disease. To address this problem, the Panel on Trace Element Geochemistry of Coal Resource Development Related to Health (PECH) was established. Certain assumptions were made by the Panel to highlight the central issues of trace elements and health and to avoid unwarranted duplication of other studies. Based on the charge to the Panel and these assumptions, this report describes the amounts and distribution of trace elements related to the coal source; the various methods of coal extraction, preparation, transportation, and use; and the disposal or recycling of the remaining residues or wastes. The known or projected health effects are discussed at the end of each section.

Not Available

1980-01-01T23:59:59.000Z

54

ADVANCED BYPRODUCT RECOVERY: DIRECT CATALYTIC REDUCTION OF SO2 TO ELEMENTAL SULFUR  

SciTech Connect

Arthur D. Little, Inc., together with its commercialization partner, Engelhard Corporation, and its university partner Tufts, investigated a single-step process for direct, catalytic reduction of sulfur dioxide from regenerable flue gas desulfurization processes to the more valuable elemental sulfur by-product. This development built on recently demonstrated SO{sub 2}-reduction catalyst performance at Tufts University on a DOE-sponsored program and is, in principle, applicable to processing of regenerator off-gases from all regenerable SO{sub 2}-control processes. In this program, laboratory-scale catalyst optimization work at Tufts was combined with supported catalyst formulation work at Engelhard, bench-scale supported catalyst testing at Arthur D. Little and market assessments, also by Arthur D. Little. Objectives included identification and performance evaluation of a catalyst which is robust and flexible with regard to choice of reducing gas. The catalyst formulation was improved significantly over the course of this work owing to the identification of a number of underlying phenomena that tended to reduce catalyst selectivity. The most promising catalysts discovered in the bench-scale tests at Tufts were transformed into monolith-supported catalysts at Engelhard. These catalyst samples were tested at larger scale at Arthur D. Little, where the laboratory-scale results were confirmed, namely that the catalysts do effectively reduce sulfur dioxide to elemental sulfur when operated under appropriate levels of conversion and in conditions that do not contain too much water or hydrogen. Ways to overcome those limitations were suggested by the laboratory results. Nonetheless, at the end of Phase I, the catalysts did not exhibit the very stringent levels of activity or selectivity that would have permitted ready scale-up to pilot or commercial operation. Therefore, we chose not to pursue Phase II of this work which would have included further bench-scale testing, scale-up, pilot-scale (0.5 MW{sub e}) testing at conditions representative of various regenerable SO{sub 2}-control systems, preparation of a commercial process design, and development of a utility-scale demonstration plan.

Robert S. Weber

1999-05-01T23:59:59.000Z

55

Trace Element Analysis At Roosevelt Hot Springs Area (Christensen, Et Al.,  

Open Energy Info (EERE)

Christensen, Et Al., Christensen, Et Al., 1983) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Trace Element Analysis At Roosevelt Hot Springs Area (Christensen, Et Al., 1983) Exploration Activity Details Location Roosevelt Hot Springs Area Exploration Technique Trace Element Analysis Activity Date Usefulness useful DOE-funding Unknown Notes Three of the recognized trace-element suites are characteristic of the surface and near-surface environment. These are: (1) concentrations of As, Sb, Be and Hg associated with siliceous material at the location of liquid discharge, fluid mixing, or at boiling interfaces; (2) deposits of Mn and Fe oxides containing concentrations of Ba, W, Be, Co, Cu, As, Sb and Hg formed by the oxidation of cooled brines; and (3) high concentrations of Hg

56

Trace Element Analysis At Northern Basin & Range Region (Coolbaugh, Et Al.,  

Open Energy Info (EERE)

At Northern Basin & Range Region (Coolbaugh, Et Al., At Northern Basin & Range Region (Coolbaugh, Et Al., 2010) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Trace Element Analysis At Northern Basin & Range Region (Coolbaugh, Et Al., 2010) Exploration Activity Details Location Northern Basin and Range Geothermal Region Exploration Technique Trace Element Analysis Activity Date Usefulness useful DOE-funding Unknown Notes "This second paper provides more detailed documentation on water and rock geochemistries and describes diagnostic major and trace element ratios and concentrations that can be used to distinguish tufa columns formed from thermal waters from those that formed from non-thermal waters." "In addition to providing a potentially diagnostic lithogeochemical tool for

57

Determination of Trace Element Concentrations at an Eastern Bituminous Coal Plant Employing an SCR and Wet FGD  

Science Conference Proceedings (OSTI)

Previous sampling has shown that air pollution control devices can have a significant impact on mercury and other trace elements. For example, selective catalytic reduction (SCR) can substantially increase the percentage of oxidized mercury that can then be removed by a wet flue gas desulfurization (FGD) system. The electrostatic precipitator (ESP) also readily captures most of the trace elements of interest. The emission of these trace elements is then directly related to the overall particulate collect...

2008-08-12T23:59:59.000Z

58

Control of Gas Tungsten Arc welding pool shape by trace element addition to the weld pool  

DOE Patents (OSTI)

An improved process for Gas Tungsten Arc welding maximizes the depth/width ratio of the weld pool by adding a sufficient amount of a surface active element to insure inward fluid flow, resulting in deep, narrow welds. The process is especially useful to eliminate variable weld penetration and shape in GTA welding of steels and stainless steels, particularly by using a sulfur-doped weld wire in a cold wire feed technique.

Heiple, C.R.; Burgardt, P.

1984-03-13T23:59:59.000Z

59

Distribution and speciation of trace elements in iron and manganese oxide cave deposits  

SciTech Connect

Fe and Mn oxide minerals control the distribution and speciation of heavy metals and trace elements in soils and aquatic systems through chemical mechanisms involving adsorption, incorporation, and electron transfer. The Pautler Cave System in Southwest Illinois, an analog to other temperate carbonate-hosted karst systems, contains Fe and Mn oxide minerals that form in multiple depositional environments and have high concentrations of associated trace elements. Synchrotron-based micro-scanning X-ray fluorescence ({mu}-SXRF) shows unique spatial distributions of Fe, Mn, and trace elements in mineral samples. Profile maps of Mn oxide cave stream pebble coatings show Fe- and As-rich laminations, indicating dynamic redox conditions in the cave stream. {mu}-SXRF maps demonstrate that Ni, Cu, and Zn correlate primarily with Mn whereas As correlates with both Mn and Fe; As is more enriched in the Fe phase. Zn is concentrated in the periphery of Mn oxide stream pebble coatings, and may be an indication of recent anthropogenic surface activity. X-ray absorption fine structure spectroscopy measurements reveal that As(V) occurs as surface complexes on Mn and Fe oxides whereas Zn(II) associated with Mn oxides is adsorbed to the basal planes of phyllomanganates in a tetrahedral coordination. Co(III) and Se(IV) are also observed to be associated with Mn oxides. The observation of Fe, Mn, and trace element banding in Mn oxide cave stream pebble coatings suggests that these materials are sensitive to and document aqueous redox conditions, similar to ferromanganese nodules in soils and in marine and freshwater sediments. Furthermore, speciation and distribution measurements indicate that these minerals scavenge trace elements and limit the transport of micronutrients and contaminants in karst aquifer systems while also potentially recording changes in anthropogenic surface activity and land-use.

Frierdich, Andrew J.; Catalano, Jeffrey G. (WU)

2012-10-24T23:59:59.000Z

60

An in situ approach to study trace element partitioning in the laser heated diamond anvil cell  

Science Conference Proceedings (OSTI)

Data on partitioning behavior of elements between different phases at in situ conditions are crucial for the understanding of element mobility especially for geochemical studies. Here, we present results of in situ partitioning of trace elements (Zr, Pd, and Ru) between silicate and iron melts, up to 50 GPa and 4200 K, using a modified laser heated diamond anvil cell (DAC). This new experimental set up allows simultaneous collection of x-ray fluorescence (XRF) and x-ray diffraction (XRD) data as a function of time using the high pressure beamline ID27 (ESRF, France). The technique enables the simultaneous detection of sample melting based to the appearance of diffuse scattering in the XRD pattern, characteristic of the structure factor of liquids, and measurements of elemental partitioning of the sample using XRF, before, during and after laser heating in the DAC. We were able to detect elements concentrations as low as a few ppm level (2-5 ppm) on standard solutions. In situ measurements are complimented by mapping of the chemical partitions of the trace elements after laser heating on the quenched samples to constrain the partitioning data. Our first results indicate a strong partitioning of Pd and Ru into the metallic phase, while Zr remains clearly incompatible with iron. This novel approach extends the pressure and temperature range of partitioning experiments derived from quenched samples from the large volume presses and could bring new insight to the early history of Earth.

Petitgirard, S.; Mezouar, M. [European Synchrotron Radiation Facility (ESRF), 6 rue Jules Horowitz, BP 220, 38043 Grenoble (France); Borchert, M.; Appel, K.; Liermann, H.-P. [Deutsches Elektronen-Synchrotron (DESY), Notkestrasse 85, 22607 Hamburg (Germany); Andrault, D. [Universite Blaise Pascal, Laboratoire des Magmas and Volcans, 5 rue Kessler 63038, Clermont-Ferrand (France)

2012-01-15T23:59:59.000Z

Note: This page contains sample records for the topic "trace elements 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

Trace Element Analysis At Long Valley Caldera Area (Klusman & Landress,  

Open Energy Info (EERE)

Klusman & Landress, Klusman & Landress, 1979) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Trace Element Analysis At Long Valley Caldera Area (Klusman & Landress, 1979) Exploration Activity Details Location Long Valley Caldera Area Exploration Technique Trace Element Analysis 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

62

Atmospheric Deposition of Mercury, Trace Elements, and Major Ions Around a Coal-fired Power Plant  

Science Conference Proceedings (OSTI)

This report describes the results of a multiyear study to measure mercury (Hg), trace elements, and major ions in precipitation around Plant Crist, a four-unit coal-fired power plant in Pensacola, Florida. The main purpose of the study was to see if Hg emissions from Plant Crist could be detected and quantified in local wet deposition. Specifically, the study evaluated whether the significant reduction in Hg emissions that accompanied the installation of a wet flue gas desulfurization scrubber ...

2013-12-22T23:59:59.000Z

63

Isotopic and trace element characteristics of rhyolites from the Valles Caldera, New Mexico. Final technical report  

DOE Green Energy (OSTI)

This report is a summary of work supported by DOE grant No. DE-FGO5-87ER13795 that was completed or is still in progress. The stated purpose of this grant was to collect geochemical information (trace element, radiogenic isotope and stable oxygen and hydrogen isotope) on samples from core holes VC-I and VC-2a in the Valles caldera in order to establish a consistent detailed intracaldera stratigraphy and relate this to extracaldera volcanic rock units of the Jemez Mountains. Careful stratigraphic control of the intracaldera units is necessary to evaluate models of caldera formation, ignimbrite deposition, and resurgence. Combined stable and radiogenic isotope and trace element data will also provide major insights to petrogenesis of the Bandelier magma system. The composition of non-hydrothermally altered samples from outflow units of the Bandelier Tuff and related volcanics must be known to assess isotopic variations of intracaldera ignimbrite samples. On detailed examination of the VC-2a core samples, it became apparent that hydrothermal alteration is so extensive that no geochemical information useful for stratigraphic fingerprinting or petrogenesis could be obtained, and that correlation with other intracaldera units and extracaldera units must be made on the basis of stratigraphic position and gross lithologic characteristics. Accordingly, we emphasize geochemical data from the extracaldera Bandelier Tuffs and related units which will be useful for comparison with proposed drill hole VC-4 and for any future studies of the region. The stable isotope, radiogenic isotope and trace element data obtained from this project, combined with existing major and trace element data for volcanic rocks from this area, provide an extensive data base essential to future Continental Scientific Drilling Program projects in the Jemez Mountains of New Mexico.

Self, S.; Sykes, M.L. [Hawaii Univ., Honolulu, HI (United States). Dept. of Geology and Geophysics; Wolff, J.A. [Texas Univ., Arlington, TX (United States). Dept. of Geology; Skuba, C.E. [McMaster Univ., Hamilton, ON (Canada). Dept. of Geology

1991-09-01T23:59:59.000Z

64

Trace Elemental Variation in Dosidicus Gigas Statoliths Using LA-ICP-MS  

E-Print Network (OSTI)

Range expansion events of the Humboldt squid reveal our inadequate understanding of populations of this species. Despite recent hatching, reproductive, tagging, genetic and dietary studies of Dosidicus gigas, much speculation remains concerning geographic migration, stock assessment and habitat preferences. This study provides evidence that statolith trace elemental variations can be useful in distinguishing among geographic populations. Specimens were collected from the Galapagos Islands, southern California, and Washington State. A dissection method was recorded and published. By using laser ablation methods, discrete measurements of 10 elements were collected at 6 to 7 ablation sites covering embryonic, paralarval, juvenile and adult stages. Analysis of Variance revealed important ontogenic elemental variations among ablation locations. Multivariate Analysis of Variance, ordination techniques and discriminant function analysis with permutation testing were all utilized to compare and characterize the variations found in elemental concentrations. Significant ontogenic variations were found for 8 out of the 10 focus elements; this is the first report for 5 of these elements for this species. The geographic populations were effectively classified as distinct group for the first time using these methods. Elemental fingerprint signatures were found to be significantly different at multiple ontogenic growth regions of the statolith. Seattle and California paralarvae exhibited similar elemental signatures despite significant differences in those found in the embryonic core and juvenile regions of the statolith. These methods are a useful tool in providing stock assessment and can be improved for use in future population dynamics models.

Arbuckle, Nancy 1980-

2012-12-01T23:59:59.000Z

65

Telling friends from foes : strontium isotope and trace element analysis of companion burials from Pusilh, Toledo District, Belize  

E-Print Network (OSTI)

Powell 1972 Strontium Isotope Geology. Minerals, Rocks, andisotope ratios in an ecosystem are a factor of the local geology andisotope and trace element values in human bone vary depending on the geology

Somerville, Andrew D.

2010-01-01T23:59:59.000Z

66

The Allegheny Power Service Constructed Wetland at Springdale: The Role of Plants in the Removal of Trace Elements  

Science Conference Proceedings (OSTI)

Constructed wetlands are proving an effective technology for the removal of many aqueous contaminants. The ability of wetlands to remove contaminants such as trace elements appears to be a function of both the physical trapping of suspended materials and the biological and chemical processes occurring within the wetlands. Thus, wetlands are commonly described as "biogeochemical reactors." This report details a study of trace element removal and sequestration within a highly engineered wetland designed to...

2001-11-05T23:59:59.000Z

67

Lubricant oil consumption effects on diesel exhaust ash emissions using a sulfur dioxide trace technique and thermogravimetry  

E-Print Network (OSTI)

A detailed experimental study was conducted targeting lubricant consumption effects on ,diesel exhaust ash levels using a model year 2002 5.9L diesel engine, high and low Sulfur commercial lubricants, and clean diesel ...

Plumley, Michael J

2005-01-01T23:59:59.000Z

68

Source characterization studies at the Paraho semiworks oil shale retort. [Redistribution of trace and major elements  

DOE Green Energy (OSTI)

In order to determine the redistribution of trace and major elements and species during aboveground oil shale retorting, a comprehensive program was carried out for the sampling and analysis of feedstock, products, effluents, and ambient particulates from the Paraho Semiworks Retort. Samples were obtained during two periods in 1977 when the retort was operating in the direct mode. The data were used to construct mass balances for 31 trace and major elements in various effluents, including the offgas. The computed mass balances indicated that approx. 1% or greater fractions of the As, Co, Hg, N, Ni, S, and Se were released during retorting and redistributed to the product oil, retort water, or product offgas. The fraction released for these seven elements ranged from approx. 1% for Co and Ni to 50 to 60% for Hg and N. Approximately 20% of the S and 5% each of the As and Se were released. Ambient aerosols were found to be elevated near the retorting facility and associated crushing and retorted shale disposal sites. Approximately 50% of these particles were in the respirable range (< 5 ..mu..m). The elevated dust loadings are presented very local, as indicated by relatively low aerosol loadings at background sites 100 to 200 m away. State-of-the-art dust control measures were not employed. 15 figures, 19 tables.

Fruchter, J.S.; Wilkerson, C.L.; Evans, J.C.; Sanders, R.W.; Abel, K.W.

1979-05-01T23:59:59.000Z

69

SULFUR POLYMER ENCAPSULATION.  

SciTech Connect

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

70

Mass balance of major and trace elements in a coal-fired power plant  

SciTech Connect

A total of 48 samples, feed coals (FCs), fly ashes (FAs) and bottom ashes (BAs), which were systematically collected once a week over an eight-week period from boiler units, B1-4 with 660 MW and B5-6 with 330 MW capacity from Soma power plant, have been evaluated for major and trace elements (Al, Ca, Fe, K, Mg, Mn, Na, Ti, S, As, B, Ba, Be, Bi, Cd, Co, Cr, Cu, Cs, Ga, Ge, Hf, Hg, Li, Mo, Nb, Ni, P, Pb, Rb, Sb, Sc, Se, Sn, Sr, Ta, Th, Tl, U, V, Y, Zn, Zr, and REEs) to get information on behavior during coal combustion. This study indicates that some elements such as Hg, Bi, Cd, As, Pb, Ge, Tl, Sn, Zn, Sb, B show enrichments in FAs relative to the BAs in both group boiler units. In addition to these, Cs, Lu, Tm, and Ga in Units B1-4 and S in Units B5-6 also have enrichments in FAs. Elements showing enrichments in BAs in both group boiler units are Ta, Mn, Nb. In addition to these, Se, Ca, Mg, Na, Fe in Units B1-4 and Cu in Units B5-6 also have enrichments in BAs. The remaining elements investigated in this study have no clear segregation between FAs and BAs. Mass balance calculations with the two methods show that some elements, S, Ta, Hg, Se, Zn, Na, Ca in Units B1-4, and Hg, S, Ta, Se, P in Units B5-6, have volatile behavior during coal combustion in the Soma power plant. This study also implies that some elements, Sb and Tb in Units B1-4 and Sb in Units B5-6, have relatively high retention effects in the combustion residues from the Soma power plant.

Karayigit, A.I.; Bulut, Y.; Karayigit, G.; Querol, X.; Alastuey, A.; Vassilev, S.; Vassileva, C. [Hacettepe University, Ankara (Turkey)

2006-10-15T23:59:59.000Z

71

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

SciTech Connect

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

72

Surface kinetic model for isotopic and trace element fractionation during precipitation of calcite from aqueous solution  

SciTech Connect

A surface reaction kinetic model is developed for predicting Ca isotope fractionation and metal/Ca ratios of calcite as a function of rate of precipitation from aqueous solution. The model is based on the requirements for dynamic equilibrium; i.e. proximity to equilibrium conditions is determined by the ratio of the net precipitation rate (R{sub p}) to the gross forward precipitation rate (R{sub f}), for conditions where ionic transport to the growing crystal surface is not rate-limiting. The value of R{sub p} has been experimentally measured under varying conditions, but the magnitude of R{sub f} is not generally known, and may depend on several factors. It is posited that, for systems with no trace constituents that alter the surface chemistry, R{sub f} can be estimated from the bulk far-from-equilibrium dissolution rate of calcite (R{sub b} or k{sub b}), since at equilibrium R{sub f} = R{sub b}, and R{sub p} = 0. Hence it can be inferred that R{sub f} {approx} R{sub p} + R{sub b}. The dissolution rate of pure calcite is measureable and is known to be a function of temperature and pH. At given temperature and pH, equilibrium precipitation is approached when R{sub p} (= R{sub f} - R{sub b}) << R{sub b}. For precipitation rates high enough that R{sub p} >> R{sub b}, both isotopic and trace element partitioning are controlled by the kinetics of ion attachment to the mineral surface, which tend to favor more rapid incorporation of the light isotopes of Ca and discriminate weakly between trace metals and Ca. With varying precipitation rate, a transition region between equilibrium and kinetic control occurs near R{sub p} {approx} R{sub b} for Ca isotopic fractionation. According to this model, Ca isotopic data can be used to estimate R{sub f} for calcite precipitation. Mechanistic models for calcite precipitation indicate that the molecular exchange rate is not constant at constant T and pH, but rather is dependent also on solution saturation state and hence R{sub p}. Allowing R{sub b} to vary as R{sub p}{sup 1/2}, consistent with available precipitation rate studies, produces a better fit to some trace element and isotopic data than a model where R{sub b} is constant. This model can account for most of the experimental data in the literature on the dependence of {sup 44}Ca/{sup 40}Ca and metal/Ca fractionation in calcite as a function of precipitation rate and temperature, and also accounts for {sup 18}O/{sup 16}O variations with some assumptions. The apparent temperature dependence of Ca isotope fractionation in calcite may stem from the dependence of R{sub b} on temperature; there should be analogous pH dependence at pH < 6. The proposed model may be valuable for predicting the behavior of isotopic and trace element fractionation for a range of elements of interest in low-temperature aqueous geochemistry. The theory presented is based on measureable thermo-kinetic parameters in contrast to models that equire hyper-fast diffusivity in near-surface layers of the solid.

DePaolo, D.

2010-10-15T23:59:59.000Z

73

Zero-order trace element distribution model for the Great Plains Coal Gasification Plant: Topical report  

SciTech Connect

The Morgantown Energy Technology Center of the US DOE is developing a series for models of environmental systems. Both zero-order and detailed models are being developed. Detailed models are based on fundamental engineering principles and the use of detailed physical and chemical property data; reliance on empirical relationships and correlations is minimized. The key advantage of detailed models is their predictive capabilities and utility in performing valid comparative analyses. An important prerequisite to the development of detailed models in the availability of representative, long-term process and environmental data. These data are needed both to develop the models as well as to validate them. Zero-order models are less rigorous and have less predictive capability than detailed models since they are based on empirical estimates and simple correlations. However, they can be developed relatively quickly and are significantly less expensive to develop and use compared to detailed models. Zero-order models are useful in identifying potential environmental or control technology problems. As such, they can help direct future research and development efforts. They can provide useful information when comprehensive data are unavailable for detailed modeling, and can be used as a screening tool to identify process alternatives which appear to warrant more detailed modeling. This report describes a zero-order trace element distribution model for the Great Plains Coal Gasification Plant located near Beulah, North Dakota. The model estimates how trace elements entering the plant in the feed coal are distributed to the plant's process and waste streams. Elements that may be introduced to the plant's waste streams from sorbents and/or catalysts (e.g., Vanadium in makeup Stretford solution) are not considered in the model. 13 refs.

Thomas, W.C.; Page, G.C.; Magee, R.A.

1987-04-01T23:59:59.000Z

74

The application of a synchrotron radiation microprobe to trace element analysis  

SciTech Connect

Synchrotron radiation is light emitted by electrons when accelerated in a circular orbit. Properties of synchrotron radiation important to trace element analysis by x-ray fluorescence analysis include a broad, continuous and tunable energy spectrum for K- and L-shell excitation of all elements; a linearly polarized source reducing the scattered radiation backgrounds; low energy deposition in the target; and an appreciable flux in narrow energy bandwidths for chemical speciation. Experiments to date have generally used ''white'' continuous spectra with a low energy absorber and no focussing, but future runs will use focussing mirrors which increase intensities by a factor of more than 1000. Monochromators will be used to select the energy and bandwidths appropriate to the experiment. Detection limits for thin biomedical samples using a solid-state detector, a 0.5 mm beam and a 5 min counting interval were in the range of 30 ppB for calcium to 50 ppB for zinc. A prototype wet cell was designed, constructed and tested using cat cardiac myocytes with the result that major trace elements such as iron could be quantitated in single myocytes. The x-ray microprobe was used to localize gallium in fetal rat bone explants after being cultured in BGJ media containing 25 ..mu..M Ga(NO/sub 3/)/sub 3/. The high brightness of x rays from a synchrotron source makes possible the development of computerized tomography on a micrometer scale. A tomogram of a freeze-dried caterpillar head was produced in a 50 min scan. The pixel size was 30 ..mu..m using a 20-..mu..m beam. 2 refs., 1 fig.

Gordon, B.M.; Hanson, A.L.; Jones, K.W.; Kwiatek, W.M.; Long, G.J.; Pounds, J.G.; Schidlovsky, G.; Spanne, P.; Rivers, M.L.; Sutton, S.R.

1987-01-01T23:59:59.000Z

75

High precision trace element and organic constituent analysis of oil shale and solvent-refined coal materials  

DOE Green Energy (OSTI)

The application of a number of sensitive and precise methods for the determination of trace elements, heavy element species and organic compounds in materials from an oil shale research retort process and from a solvent-refined coal pilot plant operation are discussed. The methods were chosen both for their sensitivity, and also for their relative freedom from interference effects. Coal liquids contain much higher concentrations of aromatic compounds, including polynuclear aromatic hydrocarbons (PNA's). A larger relative fraction of the pna's in shale oil are alkyl substituted. Coal liquids are also considerably higher in phenols (28 percent) than is shale oil (2 percent). N-heterocyclics are present in higher concentration (greater than 8 percent) in shale oil due to the high nitrogen content of the raw shale. Hydroaromatics are common in coal liquids but negligible in shale oil. Inorganic elements and speciation measurements indicate significant amounts of the toxic heavy elements Hg, As, Zn, and Se in effluent oil water and gas streams. In addition, the process water contains significant Co, Br, Sb, and U. Raw oil shale is highly enriched in Se, As and Sb and somewhat enriched in U, Pb, Cs, Hg and Zn. Solvent-refined coal liquids were found to be relatively low in most trace elements. The majority of trace elements are concentrated by the process into the mineral residue. Only Br and Hg are not depleted in solvent-refined coal. Other trace elements still remaining in significant amounts are U, Ta, Cr, and Zn.

Fruchter, J.S.; Petersen, M.R.; Laul, J.C.; Ryan, P.W.

1976-11-01T23:59:59.000Z

76

Problems of trace-element ratios and geothermometry in a gravel geothermal-aquifer system  

DOE Green Energy (OSTI)

The system studied is a Tertiary-age, block-faulted basin in which a Pleistocene gravel bed acts as a confined aquifer and permits the lateral dispersion of the geothermal fluids. Vertical movement of the hot water is currently believed to be controlled by faults on the east side of the valley. An aerial magnetic anomaly and a Bouguer gravity anomaly appear to correspond with thoese eastern faults. Basic data on the geology and trace element halos has been presented previously. Evaluation of the mixing phenomena in this system was attempted using a dissolved silica-enthalpy graph. A chalcedony curve is also plotted. An enthalpy versus chloride plot, suggests that either conductive cooling occurs before mixing or that higher chloride content background waters are available for mixing. (MHR)

Sonderegger, J.L.; Donovan, J.J.

1982-01-01T23:59:59.000Z

77

Conversion of the trace elements Zn, Cd, and Pb in the combustion of near-Moscow coals  

SciTech Connect

A model for the conversion of trace elements in the combustion of near-Moscow coals based on a complex approach combining the capabilities of geochemistry, chemical thermodynamics, phase analysis, and chemical kinetics is proposed. The conversion of the trace elements Zn, Cd, and Pb as the constituents of near-Moscow coal in the flow of coal combustion products along the line of the P-59 boiler at the Ryazanskaya Thermal Power Plant was calculated. Experimental data were used in the development of the model and in calculations.

E.V. Samuilov; L.N. Lebedeva; L.S. Pokrovskaya; M.V. Faminskaya [OAO Power Engineering Institute, Moscow (Russia)

2008-10-15T23:59:59.000Z

78

Speciation of Trace Elements in Biological and Environmental Samples by X-ray Absorption Spectroscopy: The Role of Plants and Microbes in Remediation  

Science Conference Proceedings (OSTI)

Plants can accumulate, detoxify, and transform trace elements present in contaminated soil and water, leading to the phytoremediation of contaminated sites. An important factor for consideration is the chemical form of trace elements accumulated in tissues of different plant species used for phytoremediation. This report describes the use of X-ray absorption spectroscopy (XAS) for successfully determining the speciation of trace elements in biological and environmental samples.

2001-11-21T23:59:59.000Z

79

Feasibility of the detection of trace elements in particulate matter using online High-Resolution Aerosol Mass Spectrometry  

SciTech Connect

The feasibility of using an online thermal-desorption electron-ionization high-resolution aerosol mass spectrometer (AMS) for the detection of particulate trace elements was investigated analyzing data from Mexico City obtained during the MILAGRO 2006 field campaign, where relatively high concentrations of trace elements have been reported. This potential application is of interest due to the real-time data provided by the AMS, its high sensitivity and time resolution, and the widespread availability and use of this instrument. High resolution mass spectral analysis, isotopic ratios, and ratios of different ions containing the same elements are used to constrain the chemical identity of the measured ions. The detection of Cu, Zn, As, Se, Sn, and Sb is reported. There was no convincing evidence for the detection of other trace elements commonly reported in PM. The elements detected tend to be those with lower melting and boiling points, as expected given the use of a vaporizer at 600oC in this instrument. Operation of the AMS vaporizer at higher temperatures is likely to improve trace element detection. The detection limit is estimated at approximately 0.3 ng m-3 for 5-min of data averaging. Concentration time series obtained from the AMS data were compared to concentration records determined from offline analysis of particle samples from the same times and locations by ICP (PM2.5) and PIXE (PM1.1 and PM0.3). The degree of correlation and agreement between the three instruments (AMS, ICP, and PIXE) varied depending on the element. The AMS shows promise for real-time detection of some trace elements, although additional work including laboratory calibrations with different chemical forms of these elements are needed to further develop this technique and to understand the differences with the ambient data from the other techniques. The trace elements peaked in the morning as expected for primary sources, and the many detected plumes suggest the presence of multiple point sources, probably industrial, in Mexico City which are variable in time and space, in agreement with previous studies.

Salcedo, D.; Laskin, Alexander; Shutthanandan, V.; Jimenez, Jose L.

2012-08-10T23:59:59.000Z

80

Accumulation of trace elements and growth responses in Corbicula fluminea downstream of a coal-fired power plant  

E-Print Network (OSTI)

Accumulation of trace elements and growth responses in Corbicula fluminea downstream of a coal 2009 Keywords: Corbicula fluminea Coal-fired power plant Selenium Mercury Glutathione Condition index Bioaccumulation a b s t r a c t Lentic organisms exposed to coal-fired power plant (CFPP) discharges can have

Hopkins, William A.

Note: This page contains sample records for the topic "trace elements 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

www.elsevier.com/locate/fuel Trace elements in coal derived liquids: analysis by ICP-MS and  

E-Print Network (OSTI)

Concentrations of trace elements in coal derived liquids have been investigated by inductively coupled plasma-mass spectrometry (ICP-MS) and by Mssbauer spectroscopy. Liquefaction extracts prepared from the Argonne Premium Coals and a coal tar pitch have been examined. Microwave digestion in concentrated nitric acid has been shown as a suitable method for determining trace element concentrations in coal derived liquids by ICP-MSfor sample sizes as small as 320 mg. High concentrations of Fe were found for all extract samples (?2651474 ppm). Ti, Cr, Mn, Co, Ga, Sb, Cs and Ba were measurable. Concentration distributions of trace elements found in the extracts bore little relation to the corresponding distributions in the original coals. The proportions of individual trace elements present in the original coals and found in the extracts, varied widely. Mssbauer spectroscopy of the extracts indicated that the high Fe-concentrations corresponded to the presence of organometallic-Fe compoundsand not to pyritic iron. There is evidence suggesting the presence of material derived from iron-storage proteins such as ferritin, but final proof is lacking. Our data suggest that other metallic ions detected in these coal derived liquids may be present in association with the organic material. Concentrations of paramagnetic metal species were found to be of the same order of magnitude as ESR spin-densities already found in coal liquids. Both types of paramagnetic species are suspected of causing loss of signal in

Mssbauer Spectroscopy; R. Richaud A; H. Lachas A; M. -j. Lazaro A; L. J. Clarke B; K. E. Jarvis B; A. A. Herod A; T. C. Gibb C; R. Kandiyoti A

1999-01-01T23:59:59.000Z

82

Trace element and isotope geochemistry of geothermal fluids, East Rift Zone, Kilauea, Hawaii  

DOE Green Energy (OSTI)

A research program has been undertaken in an effort to better characterize the composition and the precipitation characteristic of the geothermal fluids produced by the HGP-A geothermal well located on the Kilauea East Rift Zone on the Island of Hawaii. The results of these studies have shown that the chemical composition of the fluids changed over the production life of the well and that the fluids produced were the result of mixing of at least two, and possibly three, source fluids. These source fluids were recognized as: a sea water composition modified by high temperature water-rock reactions; meteoric recharge; and a hydrothermal fluid that had been equilibrated with high temperature reservoir rocks and magmatic volatiles. Although the major alkali and halide elements show clearly increasing trends with time, only a few of the trace transition metals show a similar trend. The rare earth elements, were typically found at low concentrations and appeared to be highly variable with time. Studies of the precipitation characteristics of silica showed that amorphous silica deposition rates were highly sensitive to fluid pH and that increases in fluid pH above about 8.5 could flocculate more than 80% of the suspended colloidal silica in excess of its solubility. Addition of transition metal salts were also found to enhance the recovery fractions of silica from solution. The amorphous silica precipitate was also found to strongly scavenge the alkaline earth and transition metal ions naturally present in the brines; mild acid treatments were shown to be capable of removing substantial fractions of the scavenged metals from the silica flocs yielding a moderately pure gelatinous by-product. Further work on the silica precipitation process is recommended to improve our ability to control silica scaling from high temperature geothermal fluids or to recover a marketable silica by-product from these fluids prior to reinjection.

West, H.B.; Delanoy, G.A.; Thomas, D.M. (Hawaii Univ., Honolulu, HI (United States). Hawaii Inst. of Geophysics); Gerlach, D.C. (Lawrence Livermore National Lab., CA (United States)); Chen, B.; Takahashi, P.; Thomas, D.M. (Hawaii Univ., Honolulu, HI (United States) Evans (Charles) and Associates, Redwood City, CA (United States))

1992-01-01T23:59:59.000Z

83

Trace elements in oil shale. Progress report, June 1, 1976--May 31, 1977  

DOE Green Energy (OSTI)

A substantial number of samples of water, stream sediment, soils, plants, oil shale, spent shale, shale oil and other materials were collected for analyses. A considerable amount of effort was also involved in the development and validation of methods for preparing and analyzing these samples for trace element content. Among the results are: Cu, Li, and Zn exhibit well-defined trends in soils over the Piceance Basin, with values increasing from north to south; As, Mo, B, and Se are all elevated in the soils of the Piceance Basin; Mo and B are more soluble in TOSCO spent shale than in unprocessed shale and are also elevated in plants growing on spent shale; F is less soluble in spent (TOSCO) shale than in unprocessed oil shale, but although the levels in leachates are quite significant (25 mg/l). F is not readily leached out; and As and Se are not very soluble in spent shale (TOSCO) and are not taken up to a significant extent by plants.

Not Available

1977-02-01T23:59:59.000Z

84

Sulfuric acid-sulfur heat storage cycle  

DOE Patents (OSTI)

A method of storing heat is provided utilizing a chemical cycle which interconverts sulfuric acid and sulfur. The method can be used to levelize the energy obtained from intermittent heat sources, such as solar collectors. Dilute sulfuric acid is concentrated by evaporation of water, and the concentrated sulfuric acid is boiled and decomposed using intense heat from the heat source, forming sulfur dioxide and oxygen. The sulfur dioxide is reacted with water in a disproportionation reaction yielding dilute sulfuric acid, which is recycled, and elemental sulfur. The sulfur has substantial potential chemical energy and represents the storage of a significant portion of the energy obtained from the heat source. The sulfur is burned whenever required to release the stored energy. A particularly advantageous use of the heat storage method is in conjunction with a solar-powered facility which uses the Bunsen reaction in a water-splitting process. The energy storage method is used to levelize the availability of solar energy while some of the sulfur dioxide produced in the heat storage reactions is converted to sulfuric acid in the Bunsen reaction.

Norman, John H. (LaJolla, CA)

1983-12-20T23:59:59.000Z

85

Washability of trace elements in product coals from Illinois mines. Technical report, 1 December 1993--28 February 1994  

DOE Green Energy (OSTI)

The existing trace element washability data on Illinois coals are based on float-sink methods, and these data are not applicable to modern froth flotation or column flotation processes. Particularly, there is a lack of washability data on samples from modern preparation plants, as well as other product (as-shipped) coals. The goal of this project is to provide the needed trace element washability data on as-shipped coals that were collected during 1992--1993 from Illinois mines. During the second quarter, froth flotation/release analysis (FF/RA) tests on 34 project samples were completed at {minus}100, {minus}200, and {minus}400 mesh particle sizes. Products from the FF/RA tests were analyzed for ash, moisture, and some for total S and heating value (BTU), and the resulting data are being used to construct a series of washability curves. For example, these curves can show variation in BTU or combustible recovery as a function of the amount of ash or S rejected. Composite samples, each having 80% of the total BTU (or combustibles), were prepared for the {minus}100 and {minus}200 mesh FF/RA tests and submitted for trace element analysis. The composite samples for the {minus}400 mesh FF/RA tests will be submitted soon, and the analytical results are expected to be available in 3--4 months. The trace element data on the composite samples will indicate the potential for the removal of each element from the coals at the chosen flotation conditions and particle sizes.

Demir, I.; Ruch, R.R.; Harvey, R.D.; Steele, J.D.; Khan, S. [Illinois State Geological Survey, Champaign, IL (United States)

1994-06-01T23:59:59.000Z

86

Method for quantitative determination and separation of trace amounts of chemical elements in the presence of large quantities of other elements having the same atomic mass  

DOE Patents (OSTI)

Photoionization via autoionizing atomic levels combined with conventional mass spectroscopy provides a technique for quantitative analysis of trace quantities of chemical elements in the presence of much larger amounts of other elements with substantially the same atomic mass. Ytterbium samples smaller than 10 ng have been detected using an ArF* excimer laser which provides the atomic ions for a time-of-flight mass spectrometer. Elemental selectivity of greater than 5:1 with respect to lutetium impurity has been obtained. Autoionization via a single photon process permits greater photon utilization efficiency because of its greater absorption cross section than bound-free transitions, while maintaining sufficient spectroscopic structure to allow significant photoionization selectivity between different atomic species. Separation of atomic species from others of substantially the same atomic mass is also described.

Miller, C.M.; Nogar, N.S.

1982-09-02T23:59:59.000Z

87

High precision trace element and organic constituent analysis of oil shale and solvent-refined coal materials  

DOE Green Energy (OSTI)

Broad spectrum inorganic and organic analytical techniques provide the best approach for the initial characterization of the complex samples encountered in working with new energy technologies such as oil shale retorting and solvent refining of coal. In complex samples, analyses are facilitated by techniques, such as neutron activation and x-ray fluorescence, that are relatively insensitive to matrix effects. A comparative organic constituent analysis of the crude shale oil and coal liquid samples analyzed in this study showed that the coal liquids contained higher concentrations of aromatic compounds including polynuclear aromatic hydrocarbons. The coal liquids were considerably richer in phenols than was the shale oil. N-heterocyclics were present in higher concentration in shale oil due to the high nitrogen content of the raw shale. Hydroaromatics were found to be common in coal liquids but negligible in this shale oil. Measurable amounts of the heavy elements Hg, As, Zn, and Se were found in effluent streams from oil shale retorting. The process water also contained significant Co, Br, Sb, and U. The raw oil shale was enriched in Se, As and Sb and somewhat enriched in U, Pb, Cs, Hg, and Zn. Solvent-refined coal liquids were found to be relatively low in most trace elements. Most were concentrated in the mineral residue. Only Br was not depleted in solvent-refined coal. Other trace elements remaining in significant amounts were U, Ta, Cr and Zn. We have not yet measured the trace elements and gaseous and particulate samples from the solvent-refined coal plant. 10 tables.

Fruchter, J.S.; Laul, J.C.; Petersen, M.R.; Ryan, P.W.

1977-03-01T23:59:59.000Z

88

Real-Time Measurements of Engine-Out Trace Elements: Application of a Novel Soot Particle Aerosol Mass Spectrometer for Emissions Characterization  

E-Print Network (OSTI)

Lubricant-derived trace element emissions are the largest contributors to the accumulation of incombustible ash in diesel particulate filters (DPF), eventually leading to filter plugging and an increase in engine fuel ...

Cross, Eben Spencer

89

Non-destructive determination of trace-element concentrations. Annual progress report, August 1979  

DOE Green Energy (OSTI)

Development and testing of the neutron-capture prompt ..gamma..-ray activation analysis method continued. A wide range of NBS Standard Reference Materials, USGS Standard Rocks, and other materials have been analyzed in order to identify elements whose lines can be observed, to determine interferences and detection limits for each important ..gamma.. ray of observable elements and to measure concentrations of observable elements for comparison with certified or other previous results. In most crustal samples, concentrations of 16 to 20 elements can be determined.

Gordon, G.E.; Zoller, W.H.; Walters, W.B.

1979-08-01T23:59:59.000Z

90

Baseline Concentrations of Radionuclides and Trace Elements in Soils and Vegetation around the DARHT Facility: Construction Phase (1998)  

Science Conference Proceedings (OSTI)

The Mitigation Action Plan for the Dual-Axis Radiographic Hydrodynamic Test (DARHT) facility at Los Alamos National Laboratory mandates the establishment of baseline concentrations for potential environmental contaminants. To this end, concentrations of {sup 3}H, {sup 137}Cs, {sup 90}Sr, {sup 238}Pu, {sup 239,240}Pu, {sup 241}Am, and {sup tot}U and Ag, As, Ba, Be, Cd, Cr, Cu, Hg, Ni, Pb, Sb, Se, and Tl were determined in surface and subsurface soils, sediments, and vegetation (overstory and understory) around the DARHT facility during the construction phase in 1998 (this is the third of a four year baseline study). Also, volatile (VOC) and semivolatile (SVOC) organic compounds were measured in soils and sediments. Most radionuclides and trace metals in soil, sediment, and vegetation were similar to past years at DARHT and were within regional background concentrations. Exceptions were concentrations of {sup 90}Sr, Be, Ba, and total U in some samples--these elements exceeded upper limit regional background concentrations (e.g., >mean plus two std dev). No VOCs and very few SVOCs were detected in soils and sediments at DARHT. Mean ({+-} std dev) radionuclide and trace element concentrations measured in soil, sediment, and vegetation summarized over a three-year period (construction phase) are summarized.

P. R. Fresquez; M. H. Ebinger; H. T. Haagenstad; L. Naranjo, Jr.

1999-12-01T23:59:59.000Z

91

Non-destructive determination of trace-element concentrations. Annual progress report  

DOE Green Energy (OSTI)

A beam port has been installed at the National Bureau of Standards (NBS) reactor by the University of Maryland group in cooperation with the NBS staff in order to initiate studies of a new analytical technique: neutron-capture prompt ..gamma..-ray activation analysis (PGAA). A detection system based on a large, high resolution Ge(Li) detector surrounded by NaI crystal has been developed for measurement of prompt ..gamma.. rays from 80 keV to 11 MeV. With a temporary external beam tube in place, neutron and ..gamma..-ray backgrounds were investigated prior to design and construction of a well-shielded beam tube and massive shielding for the detection system. With the backgrounds suitably low, it has been possible to investigate ..gamma..-ray spectra of a wide range of samples. These spectra are being carefully analyzed to identify species contributing the observed lines. Whenever an element's presence is suspected. Standards of the pure element or simple compounds are irradiated to determine its complete spectrum. This is necessary in order to determine which lines are useful for analytical purposes and which have interferences from other elements. From the results to date, it appears that PGAA will be able to measure the following elements in many types of samples: H, B, C, N, Na, Al, Si, S, Cl, K, Ca, Ti, V, Mn, Fe, Cd, Sm, and Gd. Many other elements will be measurable in certain classes of samples. Furthermore, the list of elements is incomplete, as not all lines have yet been identified in the spectra. The quantitative application of the method is being tested using a wide range of NBS Standard Reference Materials whose elemental compositions are well characterized. Measurements are reported for about fourteen elements in several standards. In general, the agreement with previous measurements is quite good.

Gordon, G.E.; Zoller, W.H.; Walters, W.B.

1978-08-01T23:59:59.000Z

92

Better Batteries from Waste Sulfur  

Science Conference Proceedings (OSTI)

Apr 28, 2013 ... Although there are some industrial uses for sulfur, the amount generated from refining fossil fuels far outstrips the current need for the element.

93

Biological processes for concentrating trace elements from uranium mine waters. Technical completion report  

Science Conference Proceedings (OSTI)

Waste water from uranium mines in the Ambrosia Lake district near Grants, New Mexico, USA, contains uranium, selenium, radium and molybdenum. The Kerr-McGee Corporation has a novel treatment process for waters from two mines to reduce the concentrations of the trace contaminants. Particulates are settled by ponding, and the waters are passed through an ion exchange resin to remove uranium; barium chloride is added to precipitate sulfate and radium from the mine waters. The mine waters are subsequently passed through three consecutive algae ponds prior to discharge. Water, sediment and biological samples were collected over a 4-year period and analyzed to assess the role of biological agents in removal of inorganic trace contaminants from the mine waters. Some of the conclusions derived from this study are: (1) The concentrations of soluble uranium, selenium and molybdenum were not diminished in the mine waters by passage through the series of impoundments which constituted the mine water treatment facility. Uranium concentrations were reduced but this was due to passage of the water through an ion exchange column. (2) The particulate concentrations of the mine water were reduced at least ten-fold by passage of the waters through the impoundments. (3) The sediments were anoxic and enriched in uranium, molybdenum and selenium. The deposition of particulates and the formation of insoluble compounds were proposed as mechanisms for sediment enrichment. (4) The predominant algae of the treatment ponds were the filamentous Spirogyra and Oscillatoria, and the benthic alga, Chara. (5) Adsorptive processes resulted in the accumulation of metals in the algae cells. (6) Stimulation of sulfate reduction by the bacteria resulted in retention of molybdenum, selenium, and uranium in sediments. 1 figure, 16 tables.

Brierley, C.L.; Brierley, J.A.

1981-12-01T23:59:59.000Z

94

Quantifying the availability and the stability of trace cationic elements in fly ash  

E-Print Network (OSTI)

-Products Associated with Coal Mining Interactive Forum: Southern Illinois University at Carbondale, Carbondale, IL in this paper to deter- mine these parameters for model elements Cu(II), Cd(II), and Ni(II) in fly ash 50 mM EDTA extraction. ? 2006 Elsevier Ltd. All rights reserved. 1. Introduction Coal fly ash has

Ragsdell, Kenneth M.

95

Process for the elimination of waste water produced upon the desulfurization of coking oven gas by means of wash solution containing organic oxygen-carrier, with simultaneous recovery of elemental sulfur  

Science Conference Proceedings (OSTI)

A process is disclosed for the elimination of waste water falling out with the desulfurization of coking oven gas by means of an organic oxygen carrier-containing washing solution with simultaneous recovery of elemental sulfur. The waste water is decomposed in a combustion chamber in a reducing atmosphere at temperatures between about 1000/sup 0/ and 1100/sup 0/ C. under such conditions that the mole ratio of H/sub 2/S:SO/sub 2/ in the exhaust gas of the combustion chamber amounts to at least 2:1. Sulfur falling out is separated and the sensible heat of the exhaust gas is utilized for steam generation. The cooled and desulfurized exhaust gas is added to the coking oven gas before the pre-cooling. Sulfur falling out from the washing solution in the oxidizer is separated out and lead into the combustion chamber together with the part of the washing solution discharged as waste water from the washing solution circulation. Preferred embodiments include that the sulfur loading of the waste water can amount to up to about 370 kg sulfur per m/sup 3/ waste water; having the cooling of sulfur-containing exhaust gas leaving the combustion chamber follow in a waste heat boiler and a sulfur condenser heated by pre-heated boiler feed water, from which condenser sulfur is discharged in liquid state.

Diemer, P.; Brake, W.; Dittmer, R.

1985-04-16T23:59:59.000Z

96

Advanced byproduct recovery: Direct catalytic reduction of sulfur dioxide to elemental sulfur. Second quarterly technical progress report, January--March 1996  

SciTech Connect

In the more than 170 wet scrubber systems in 72,000 MW of US, coal-fired, utility boilers, the SO{sub 2} removed from the boiler flue gas is sorbed, and the sulfated sorbent must be disposed of. The use of regenerable sorbents has the potential to reduce this disposal problem. The team of Arthur D. Little, Tufts Univ., and Engelhard Corp. are conducting Phase I of a 4.5-year, two-phase effort to develop and scale-up a direct, single-stage, catalytic process for converting SO{sub 2} to S. This catalytic process reduces SO{sub 2} over a fluorite-type oxide such as ceria and zirconia; the catalytic activity can be promoted by active transition metals such as Cu. The Phase I program includes the following work elements: market/process/cost/evaluation; lab-scale catalyst preparation/optimization, lab-scale bulk/supported catalyst kinetic studies, bench-scale catalyst/process studies, and utility review.

1996-05-01T23:59:59.000Z

97

Lithium/Sulfur Batteries Based on Doped Mesoporous Carbon ...  

A sulfur/carbon composite material was prepared by heat treatment of doped mesoporous carbon and elemental sulfur at a temperature inside a stainless steel vessel ...

98

Trace species emissions for IGFC  

SciTech Connect

The objectives of this investigation are to study both the fate and distribution of at least five significant, coal-derived trace elements commonly present in coal-gas, in terms of their vaporization during gasification, their condensation and sorption during hot-gas cleanup, as well as their effects on fuel cells, gas turbines, and ultimately the environment. The definition here of trace does not include the major contaminants of sulfur and chlorine, etc., although the simultaneous presence of such major species is always considered in our thermochemical calculations. Of course, many other elements can vaporize in trace quantities from raw coal as either volatile, molecular compounds or as metallic vapors which, besides their deleterious action on the energy conversion systems, can also be detrimental to plant and animal life when emitted into the atmosphere. Hence, an understanding is sought of how the type and quantity of significant trace species in coal-gas changes from the coal pile through cleanup subsystems and the electric generators to the exhaust stack of an integrated system.

Pigeaud, A.E.; Helble, J.J.

1994-10-01T23:59:59.000Z

99

Bacterial Sulfur Storage Globules  

NLE Websites -- All DOE Office Websites (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.

100

Sodium sulfur battery seal  

SciTech Connect

This invention is directed to a seal for a sodium sulfur battery in which a flexible diaphragm sealing elements respectively engage opposite sides of a ceramic component of the battery which separates an anode compartment from a cathode compartment of the battery.

Topouzian, Armenag (Birmingham, MI)

1980-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "trace elements 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

Sulfur condensation in Claus catalyst  

SciTech Connect

The heterogeneous reactions in which catalyst deactivation by pore plugging occur are listed and include: coke formation in petroleum processing, especially hydrocracking and hydrodesulfurization catalysts; steam reforming and methnation catalysts; ammonia synthesis catalyst; and automobile exhause catalysts. The authors explain how the Claus process converts hydrogen sulfide produced by petroleum desulfurization units and gas treatment processes into elemental sulfur and water. More than 15 million tons of sulfur are recovered annually by this process. Commercial Claus plants appear to operate at thermodynamic equilibrium. Depending on the H2S content of the feed and the number of reactors, total H2S conversion to elemental sulfur can exceed 95%.

Schoffs, G.R.

1985-02-01T23:59:59.000Z

102

PARTITIONING OF MAJOR, MINOR, AND TRACE ELEMENTS DURING SIMULATED IN SITU OIL SHALE RETORTING IN A CONTROLLED-STATE RETORT  

E-Print Network (OSTI)

produce oil, in various gas, bitumen, and C quantities andquantity of each element distributed among the products and Elements in the oilOil shales contain organic material in a mineral matrix which includes significant environmentally As, quantities

Fox, J. P.

2011-01-01T23:59:59.000Z

103

Economic feasibility of biochemical processes for the upgrading of crudes and the removal of sulfur, nitrogen, and trace metals from crude oil -- Benchmark cost establishment of biochemical processes on the basis of conventional downstream technologies. Final report FY95  

Science Conference Proceedings (OSTI)

During the past several years, a considerable amount of work has been carried out showing that microbially enhanced oil recovery (MEOR) is promising and the resulting biotechnology may be deliverable. At Brookhaven National Laboratory (BNL), systematic studies have been conducted which dealt with the effects of thermophilic and thermoadapted bacteria on the chemical and physical properties of selected types of crude oils at elevated temperatures and pressures. Current studies indicate that during the biotreatment several chemical and physical properties of crude oils are affected. The oils are (1) emulsified; (2) acidified; (3) there is a qualitative and quantitative change in light and heavy fractions of the crudes; (4) there are chemical changes in fractions containing sulfur compounds; (5) there is an apparent reduction in the concentration of trace metals; and (6) the qualitative and quantitative changes appear to be microbial species dependent; and (7) there is a distinction between biodegraded and biotreated oils. The downstream biotechnological crude oil processing research performed thus far is of laboratory scale and has focused on demonstrating the technical feasibility of downstream processing with different types of biocatalysts under a variety of processing conditions. Quantitative economic analysis is the topic of the present project which investigates the economic feasibility of the various biochemical downstream processes which hold promise in upgrading of heavy crudes, such as those found in California, e.g., Monterey-type, Midway Sunset, Honda crudes, and others.

Premuzic, E.T.

1996-08-01T23:59:59.000Z

104

Why Sequence Sulfur-Oxidizing Bacteria?  

NLE Websites -- All DOE Office Websites (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

105

PARTITIONING OF MAJOR, MINOR, AND TRACE ELEMENTS DURING SIMULATED IN SITU OIL SHALE RETORTING IN A CONTROLLED-STATE RETORT  

E-Print Network (OSTI)

elements. Over 25% of the raw shale gas five groups productsthe oil, in the raw oil shale gas, consequence of retortinggood product raw oil shale and input gases that is accounted

Fox, J. P.

2011-01-01T23:59:59.000Z

106

Multiple-sulfur isotope effects during photolysis of carbonyl sulfide  

E-Print Network (OSTI)

Laboratory experiments were carried out to determine sulfur isotope effects during ultraviolet photolysis of carbonyl sulfide (OCS) to carbon monoxide (CO) and elemental sulfur (S[superscript 0]). The OCS gas at 3.7 to 501 ...

Lin, Ying

107

Microwave assisted sulfur infusion technique and the corresponding ...  

Science Conference Proceedings (OSTI)

Abstract Scope, Li-S battery is quite attractive due to the usage of elemental sulfur as cathode. The theoretical capacity of sulfur cathode is 1672 mAh/g, which

108

Uncertainty Measurement for Trace Element Analysis of Uranium and Plutonium Samples by Inductively Coupled Plasma-Atomic Emission Spectrometry (ICP-AES) and Inductively Coupled Plasma-Mass Spectrometry (ICP-MS)  

Science Conference Proceedings (OSTI)

The measurement uncertainty estimatino associated with trace element analysis of impurities in U and Pu was evaluated using the Guide to the Expression of Uncertainty Measurement (GUM). I this evalution the uncertainty sources were identified and standard uncertainties for the components were categorized as either Type A or B. The combined standard uncertainty was calculated and a coverage factor k = 2 was applied to obtain the expanded uncertainty, U. The ICP-AES and ICP-MS methods used were deveoped for the multi-element analysis of U and Pu samples. A typical analytical run consists of standards, process blanks, samples, matrix spiked samples, post digestion spiked samples and independent calibration verification standards. The uncertainty estimation was performed on U and Pu samples that have been analyzed previously as part of the U and Pu Sample Exchange Programs. Control chart results and data from the U and Pu metal exchange programs were combined with the GUM into a concentration dependent estimate of the expanded uncertainty. Comparison of trace element uncertainties obtained using this model was compared to those obtained for trace element results as part of the Exchange programs. This process was completed for all trace elements that were determined to be above the detection limit for the U and Pu samples.

Gallimore, David L. [Los Alamos National Laboratory

2012-06-13T23:59:59.000Z

109

Trace element and REE composition of five samples of the Yucca Mountain calcite-silica deposits. Special report No. 8  

SciTech Connect

The attached materials document the results of part of a recent effort of geochemical sampling and analysis at Yucca Mountain and nearby regions. The efforts come as a result of interest in comprehensive analyses of rare earth elements (REE), lanthanum (La) through lutecium (Lu). Several additional, non-REE analyses were obtained as well. Commercially available REE analyses have proved to be insufficiently sensitive for geochemical purposes. Dr. Roman Schmitt at the Radiation Center at Oregon State University in Corvallis was sent five samples as a trial effort. The results are very encouraging. The purpose of compiling Dr. Schmitt`s report and the other materials is to inform the sponsor of his independent observations of these results and other information that sent to him. To provide a more complete appreciation of the utility of REE analyses a copy of Dave Vaniman`s recent article is included in which he notes that REE analyses from Yucca Mountain indicate the occurrence of two distinctly different REE patterns as do several other chemical parameters of the calcite-silica deposits. Our four samples with high equivalent CaCO{sub 3} were collected from sites we believe to be spring deposits. One sample, 24D, is from southern Crater Flat which is acknowledged by U.S.G.S. investigators to be a spring deposit. All four of these samples have REE patterns similar to those from the saturated zone reported by Vaniman.

Livingston, D.

1993-07-01T23:59:59.000Z

110

Fractionation of sulfur isotopes by Desulfovibrio vulgaris mutants lacking hydrogenases or type I tetraheme cytochrome c[subscript 3  

E-Print Network (OSTI)

The sulfur isotope effect produced by sulfate reducing microbes is commonly used to trace biogeochemical cycles of sulfur and carbon in aquatic and sedimentary environments. To test the contribution of intracellular coupling ...

Sim, Min Sub

111

Trace metal transformation in gasification  

SciTech Connect

The Energy & Environmental Research Center (EERC) is carrying out an investigation that will provide methods to predict the fate of selected trace elements in integrated gasification combined cycle (IGCC) and integrated gasification fuel cell (IGFC) systems to aid in the development of methods to control the emission of trace elements determined to be air toxics. The goal of this project is to identify the effects of critical chemical and physical transformations associated with trace element behavior in IGCC and IGFC systems. The trace elements included in this project are arsenic, chromium, cadmium, mercury, nickel, selenium, and lead. The research seeks to identify and fill, experimentally and/or theoretically, data gaps that currently exist on the fate and composition of trace elements. The specific objectives are to 1) review the existing literature to identify the type and quantity of trace elements from coal gasification systems, 2) perform laboratory-scale experimentation and computer modeling to enable prediction of trace element emissions, and 3) identify methods to control trace element emissions.

Benson, S.A.; Erickson, T.A.; Zygarlicke, C.J.; O`Keefe, C.A.; Katrinak, K.A.; Allen, S.E.; Hassett, D.J.; Hauserman, W.B. [North Dakota Univ., Grand Forks, ND (United States). Energy and Environmental Research Center; Holcombe, N.T. [USDOE Morgantown Energy Technology Center, WV (United States)

1996-12-31T23:59:59.000Z

112

Trace metal transformations in gasification  

SciTech Connect

The Energy & Environmental Research Center (EERC) is carrying out an investigation that will provide methods to predict the fate of selected trace elements in integrated gasification combined cycle (IGCC) and integrated gasification fuel cell (IGFC) systems to aid in the development of methods to control the emission of trace elements determined to be air toxics. The goal of this project is to identify the effects of critical chemical and physical transformations associated with trace element behavior in IGCC and IGFC systems. The trace elements included in this project are arsenic, chromium, cadmium, mercury, nickel, selenium, and lead. The research seeks to identify and fill, experimentally and/or theoretically, data gaps that currently exist on the fate and composition of trace elements. The specific objectives are to (1) review the existing literature to identify the type and quantity of trace elements from coal gasification systems, (2) perform laboratory-scale experimentation and computer modeling to enable prediction of trace element emissions, and (3) identify methods to control trace element emissions.

Benson, S.; Erickson, T.A.; Zygarlicke, C.J. [and others

1995-12-01T23:59:59.000Z

113

It's Elemental - The Element Phosphorus  

NLE Websites -- All DOE Office Websites (Extended Search)

Silicon Silicon Previous Element (Silicon) The Periodic Table of Elements Next Element (Sulfur) Sulfur The Element Phosphorus [Click for Isotope Data] 15 P Phosphorus 30.973762 Atomic Number: 15 Atomic Weight: 30.973762 Melting Point: 317.30 K (44.15°C or 111.47°F) Boiling Point: 553.65 K (280.5°C or 536.9°F) Density: 1.82 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Non-metal Period Number: 3 Group Number: 15 Group Name: Pnictogen What's in a name? From the Greek word for light bearing, phosphoros. Say what? Phosphorus is pronounced as FOS-fer-es. History and Uses: In what is perhaps the most disgusting method of discovering an element, phosphorus was first isolated in 1669 by Hennig Brand, a German physician and alchemist, by boiling, filtering and otherwise processing as many as 60

114

Abstracts from a workshop on processes determining the input, behavior and fate of radionuclides and trace elements in continental shelf environments  

Science Conference Proceedings (OSTI)

Abstracts of workshop presentations concerning input, behavior, and fate of trace metals and radionuclides in the marine system are presented. (ACR)

Not Available

1980-03-01T23:59:59.000Z

115

Uranium Trace Elements Erik Hunter  

E-Print Network (OSTI)

be made. The electroscope relied upon the ability of the gamma radiation emitted by the sample to ionize that prove anomalous in the field can be subjected to more accurate tests in the lab that will determine #12;associated with the device was reported to be +/- 4% of the actual uranium content in the sample

116

Production of elemental sulfur and methane from H{sub 2}S and CO{sub 2} derived from a coal desulfurization process. Final report, September 1, 1993--March 31, 1997  

DOE Green Energy (OSTI)

The purpose of this study was to experimentally and theoretically investigate the feasibility of producing elemental sulfur, carbon monoxide, hydrogen and possible methane from hydrogen sulfide and carbon dioxide through catalytic reactions. A novel experimental system that could evaluate potential catalysts and adsorbents under controlled laboratory conditions was designed and constructed. Additionally an effective simulation program capable of providing valuable thermodynamic information on the reaction system was compiled. The following tasks have been performed: (1) design and construction of an experimental system for the catalyst preparation and catalyst screening studies including frequent modifications of the experimental setup to meet specific application needs; (2) installation and calibration of related analytical instruments, and investigation of the temperature distribution profile inside the reactor; (3) preparation, reduction, sulfidation of potential catalysts, and measurements of specific surface area of catalysts; (4) decomposition of H{sub 2}S under both non-catalytic condition and catalytic condition with the CoO-MoO{sub 3}-alumina catalyst at moderate temperatures around 550 C. Analyses of the product gas by gas chromatograph; and (5) thermodynamic studies on the theoretical conversions of H{sub 2}S for various temperatures, pressures and ratios of H{sub 2}S to CO{sub 2}. Based on the results of the above tasks, bench scale experiments were performed with the CoO-MoO{sub 3}-alumina catalyst at moderate temperatures around 550 C to investigate the adsorption effects of solid sorbents in order to remove sulfur from the reaction environment. Four kinds of adsorbents have been tested along with several designs of solid adsorbent feed systems.

Jiang, X.; Khang, S.J.; Keener, T.C.

1997-12-31T23:59:59.000Z

117

ARM - Measurement - Trace gas concentration  

NLE Websites -- All DOE Office Websites (Extended Search)

govMeasurementsTrace gas concentration govMeasurementsTrace gas concentration ARM Data Discovery Browse Data Comments? We would love to hear from you! Send us a note below or call us at 1-888-ARM-DATA. Send Measurement : Trace gas concentration The amount per unit volume of trace gases other than carbon dioxide, ozone and water vapor, typically measured in conjunction with in situ aerosol measurements, e.g. carbon monoxide, nitrogen oxides, sulfur dioxide. Categories Atmospheric Carbon, Atmospheric State Instruments The above measurement is considered scientifically relevant for the following instruments. Refer to the datastream (netcdf) file headers of each instrument for a list of all available measurements, including those recorded for diagnostic or quality assurance purposes. ARM Instruments CO : Carbon Monoxide Mixing Ratio System

118

Neogene Low-latitude Seasonal Environmental Variations: Stable Isotopic and Trace Elemental Records in Mollusks from the Florida Platform and the Central American Isthmus  

E-Print Network (OSTI)

This Ph.D. dissertation integrates stable isotope and trace element geochemistry in modern and fossil gastropod shells to study low-latitude marine paleoenvironments. First, stable isotopes (delta18O and delta13C) and Sr/Ca ratios are used to examine low-latitude temperature and salinity variations recorded in Plio-Pleistocene (3.5-1.6 Ma) fossils from western Florida during periods of high-latitude warming and "global" cooling. The middle Pliocene Pinecrest Beds (Units 7 and 4) and the overlaying Plio-Pleistocene Caloosahatchee Formation generate significantly different delta18O-derived paleotemperatures but identical Sr/Ca ratios. High delta18O values, together with low delta13C values and brackish fauna, indicate that Unit 4 was deposited in a lagoonal environment similar to modern Florida Bay. In contrast, relatively low delta18O and high delta13C values in Unit 7 and Caloosahatchee Formation represent deposition in an open-marine environment. The observed Unit 7 and Caloosahatchee paleotemperatures are inconsistent with middle Pliocene warming event, but consistent with the Plio-Pleistocene cooling trend. To quantify modern upwelling and freshening signals and contrast these signals between the tropical eastern Pacific (TEP) and southwestern Caribbean (SWC), methodologies are developed for reconstructing seasonal upwelling and freshening patterns from modern tropical gastropod shells from Panama using: 1) paired oxygen and carbon isotopic profiles and delta18O-delta13C (delta-delta) correlations, and 2) deviation from baseline delta18O values that represent conditions free of seasonal upwelling or freshening influences. Shell delta18O values normalized to the baseline faithfully record modern conditions of little or no upwelling in SWC and Gulf of Chiriqui, and strong upwelling in the Gulf of Panama, as well as strong freshwater input in most areas. The baseline and delta-delta methods are applied to identify and quantify changes in upwelling and freshening in the Neogene TEP and SWC seawaters associated with the final closure of Central American Isthmus. The records reveal significant upwelling in late Miocene SWC and mid Pliocene TEP waters, strong freshening in SWC waters from 5.7-2.2 Ma, and minimal seasonal upwelling and/or freshening variations in Plio-Pleistocene SWC waters. The reconstructed paleotemperatures agree with the global cooling trend through the late Miocene, but lack evidence for middle Pliocene warming or late Neogene global cooling.

Tao, Kai

2012-08-01T23:59:59.000Z

119

Selected elemental distributions as determined by reference retorting of oil shale  

DOE Green Energy (OSTI)

In an effort to determine potential hindrances to the commercial development of the oil shale industry mass balance Fischer assay was used as a reference retorting method to examine the distribution of selected elements generally considered as contaminants in the final retort products. The elements examined were nitrogen, sulfur, silver, arsenic, barium, cadmium, chromium, copper, mercury, lead, selenium, and zinc. The shales used in this study were an eastern (New Albany) interim reference shale, a western (Green River Formation) interim reference shale, and a series of stratigraphically differentiated shales from Colorado corehole No. 1 in the Piceance Creek Basin. Analysis of the raw shale and retort products was accomplished using instrumental elemental methods including inductively coupled argon plasma spectroscopy and graphite furnace atomic absorption. Carbon balances indicated a high potential for achieving good mass closures existed. However, instrumental limitations combined with a high potential for contamination and/or representative sampling problems resulted in poor closures for many of the trace elements. Consistent closures were obtained for arsenic, barium, copper, and zinc. Given the operating conditions of the retort all elements under consideration remained primarily in the spent shale. Elements verified in the oil product included nitrogen and sulfur compounds and arsenic and selenium. The water product was also contaminated by nitrogen and sulfur compounds and arsenic and selenium. Evidence suggests the sulfur occurs primarily as organic sulfur. Quantitative results for the gas product were poor. However, sulfur and mercury were determined to be present at significant levels in the gas stream. The data presented here concurs with previously reported data that suggests the existence of several potential problem areas in the development of an oil shale industry. 42 refs., 1 fig., 42 tabs.

Johnson, L.S.

1986-07-01T23:59:59.000Z

120

It's Elemental - The Element Chlorine  

NLE Websites -- All DOE Office Websites (Extended Search)

Sulfur Sulfur Previous Element (Sulfur) The Periodic Table of Elements Next Element (Argon) Argon The Element Chlorine [Click for Isotope Data] 17 Cl Chlorine 35.453 Atomic Number: 17 Atomic Weight: 35.453 Melting Point: 171.65 K (-101.5°C or -150.7°F) Boiling Point: 239.11 K (-34.04°C or -29.27°F) Density: 0.003214 grams per cubic centimeter Phase at Room Temperature: Gas Element Classification: Non-metal Period Number: 3 Group Number: 17 Group Name: Halogen What's in a name? From the Greek word for greenish yellow, chloros. Say what? Chlorine is pronounced as KLOR-een or as KLOR-in. History and Uses: Since it combines directly with nearly every element, chlorine is never found free in nature. Chlorine was first produced by Carl Wilhelm Scheele, a Swedish chemist, when he combined the mineral pyrolusite (MnO2) with

Note: This page contains sample records for the topic "trace elements 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

Trace Evidence  

Science Conference Proceedings (OSTI)

... Work with national and international ... 00 Optional Open House and Trace Analysis Lab Tours of ... Ethanol in Water Standard Reference Materials to ...

2012-12-06T23:59:59.000Z

122

Sulfur tolerant anode materials  

DOE Green Energy (OSTI)

The goal of this program is the development of a molten carbonate fuel cell (MCFC) anode which is more tolerant of sulfur contaminants in the fuel than the current state-of-the-art nickel-based anode structures. This program addresses two different but related aspects of the sulfur contamination problem. The primary aspect is concerned with the development of a sulfur tolerant electrocatalyst for the fuel oxidation reaction. A secondary issue is the development of a sulfur tolerant water-gas-shift reaction catalyst and an investigation of potential steam reforming catalysts which also have some sulfur tolerant capabilities. These two aspects are being addressed as two separate tasks.

Not Available

1988-05-01T23:59:59.000Z

123

It's Elemental - Isotopes of the Element Chlorine  

NLE Websites -- All DOE Office Websites (Extended Search)

Sulfur Sulfur Previous Element (Sulfur) The Periodic Table of Elements Next Element (Argon) Argon Isotopes of the Element Chlorine [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 35 75.76% STABLE 37 24.24% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 28 No Data Available Proton Emission (suspected) No Data Available 29 < 20 nanoseconds Proton Emission No Data Available 30 < 30 nanoseconds Proton Emission No Data Available 31 150 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 0.70% 32 298 milliseconds Electron Capture 100.00%

124

Removal of pyrite and trace elements from waste coal by dissolved-CO{sub 2} flotation and chelating agents. [Quarterly] technical report, December 1, 1993--February 28, 1994  

SciTech Connect

In dissolved-CO{sub 2} flotation, ultrafine -bubbles are generated by CO{sub 2} dissolved in water. The ultrafine bubbles have the potential to improve the separation efficiency in fine coal cleaning. Chemicals will be used prior to or during dissolved-CO{sub 2} flotation to improve the separation efficiency-CO{sub 2} of pyrite and other minerals including trace metals from coal. Chelating agent will be applied to clean coal to further reduce the trace metals from coal. During this period, a 3 in. diameter packed column has been purchased and installed. This column was then modified for use in dissolved-CO{sub 2} flotation. Coal samples of Illinois No. 6 coal are being prepared for flotation. Preliminary flotation tests were performed on Illinois No. 6 waste coal.

Shiao, S.Y. [Babcock and Wilcox Company (United States)

1994-08-01T23:59:59.000Z

125

Removal of pyrite and trace elements from waste coal by dissolved- CO{sub 2} flotation and chelating agents. Technical report, September 1, 1993--November 30, 1993  

SciTech Connect

In dissolved-CO{sub 2} flotation, ultrafine bubbles are generated by CO{sub 2} dissolved in water. The ultrafine bubbles have the potential to improve the separation efficiency in fine coal cleaning. Chemicals will be used prior to or during dissolved-CO{sub 2} flotation to improve the separation efficiency of pyrite and other minerals including trace metals from coal. Chelating agents will be applied to clean coal to further reduce the trace metals from coal. During this period, the project planning has begun. A 3in.-diameter packed column has been ordered. This column will be modified for use in dissolved-CO{sub 2} flotation. Clean and waste coal samples of Illinois No. 6 coal have been scheduled to be picked up from Ohio Coal Testing and Development (OCTAD) facility.

Shiao, S.Y. [Babcock and Wilcox Co., Alliance, OH (United States)

1993-12-31T23:59:59.000Z

126

Ultra-Low Sulfur Diesel  

NLE Websites -- All DOE Office Websites (Extended Search)

Ultra-Low Sulfur Diesel ULSD LSD Off-Road Ultra-Low Sulfur Highway Diesel Fuel (15 ppm Sulfur Maximum). Required for use in all model year 2007 and later highway diesel vehicles...

127

Distribution and origin of sulfur in Colorado oil shale  

SciTech Connect

The sulfur content of 1,225 samples of Green River oil shale from two core holes in the Piceance Creek Basin, Colorado, ranges from nearly 0 to 4.9 weight percent. In one core hole, the average sulfur content of a sequence of oil shale 555 m thick, which represents nearly the maximum thickness of oil shale in the basin, is 0.76 weight percent. The vertical distribution of sulfur through the oil shale is cyclic. As many as 25 sulfur cycles have lateral continuity and can be traced between the core holes. Most of the sulfur resides in iron sulfides (pyrite, marcasite, and minor. pyrrhotite), and small amounts are organically bound in kerogen. In general, the concentration of sulfur correlates moderately with oil shale yield, but the degree of association ranges from quite high in the upper 90 m of the oil shale sequence to low or none in the leached zone and in illitic oil shale in the lower part of the sequence. Sulfur also correlates moderately with iron in the carbonate oil shale sequence, but no correlation was found in the illitic samples. Sulfide mineralization is believed to have occurred during early and late stages of diagenesis, and after lithification, during development of the leached zone. Significant amounts of iron found in ankeritic dolomite and in illite probably account for the lack of a strong correlation between sulfur and iron.

Dyni, J.R.

1983-04-01T23:59:59.000Z

128

Provenance Traces  

E-Print Network (OSTI)

Provenance is information about the origin, derivation, ownership, or history of an object. It has recently been studied extensively in scientific databases and other settings due to its importance in helping scientists judge data validity, quality and integrity. However, most models of provenance have been stated as ad hoc definitions motivated by informal concepts such as "comes from", "influences", "produces", or "depends on". These models lack clear formalizations describing in what sense the definitions capture these intuitive concepts. This makes it difficult to compare approaches, evaluate their effectiveness, or argue about their validity. We introduce provenance traces, a general form of provenance for the nested relational calculus (NRC), a core database query language. Provenance traces can be thought of as concrete data structures representing the operational semantics derivation of a computation; they are related to the traces that have been used in self-adjusting computation, but differ in impor...

Cheney, James; Ahmed, Amal

2008-01-01T23:59:59.000Z

129

It's Elemental - The Element Indium  

NLE Websites -- All DOE Office Websites (Extended Search)

Cadmium Cadmium Previous Element (Cadmium) The Periodic Table of Elements Next Element (Tin) Tin The Element Indium [Click for Isotope Data] 49 In Indium 114.818 Atomic Number: 49 Atomic Weight: 114.818 Melting Point: 429.75 K (156.60°C or 313.88°F) Boiling Point: 2345 K (2072°C or 3762°F) Density: 7.31 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 5 Group Number: 13 Group Name: none What's in a name? Named after the bright indigo line in its spectrum. Say what? Indium is pronounced as IN-dee-em. History and Uses: Indium was discovered by the German chemists Ferdinand Reich and Hieronymus Theodor Richter in 1863. Reich and Richter had been looking for traces of the element thallium in samples of zinc ores. A brilliant indigo line in

130

Sulfur Dioxide Regulations (Ohio)  

Energy.gov (U.S. Department of Energy (DOE))

This chapter of the law establishes that the Ohio Environmental Protection Agency provides sulfur dioxide emission limits for every county, as well as regulations for the emission, monitoring and...

131

Separation of sulfur isotopes  

DOE Patents (OSTI)

Sulfur isotopes are continuously separated and enriched using a closed loop reflux system wherein sulfur dioxide (SO.sub.2) is reacted with sodium hydroxide (NaOH) or the like to form sodium hydrogen sulfite (NaHSO.sub.3). Heavier sulfur isotopes are preferentially attracted to the NaHSO.sub.3, and subsequently reacted with sulfuric acid (H.sub.2 SO.sub.4) forming sodium hydrogen sulfate (NaHSO.sub.4) and SO.sub.2 gas which contains increased concentrations of the heavier sulfur isotopes. This heavy isotope enriched SO.sub.2 gas is subsequently separated and the NaHSO.sub.4 is reacted with NaOH to form sodium sulfate (Na.sub.2 SO.sub.4) which is subsequently decomposed in an electrodialysis unit to form the NaOH and H.sub.2 SO.sub.4 components which are used in the aforesaid reactions thereby effecting sulfur isotope separation and enrichment without objectionable loss of feed materials.

DeWitt, Robert (Centerville, OH); Jepson, Bernhart E. (Dayton, OH); Schwind, Roger A. (Centerville, OH)

1976-06-22T23:59:59.000Z

132

A portable optical emission spectroscopy-cavity ringdown spectroscopy dual-mode plasma spectrometer for measurements of environmentally important trace heavy metals: Initial test with elemental Hg  

SciTech Connect

A portable optical emission spectroscopy-cavity ringdown spectroscopy (OES-CRDS) dual-mode plasma spectrometer is described. A compact, low-power, atmospheric argon microwave plasma torch (MPT) is utilized as the emission source when the spectrometer is operating in the OES mode. The same MPT serves as the atomization source for ringdown measurements in the CRDS mode. Initial demonstration of the instrument is carried out by observing OES of multiple elements including mercury (Hg) in the OES mode and by measuring absolute concentrations of Hg in the metastable state 6s6p {sup 3}P{sub 0} in the CRDS mode, in which a palm-size diode laser operating at a single wavelength 405 nm is incorporated in the spectrometer as the light source. In the OES mode, the detection limit for Hg is determined to be 44 parts per 10{sup 9} (ppb). A strong radiation trapping effect on emission measurements of Hg at 254 nm is observed when the Hg solution concentration is higher than 50 parts per 10{sup 6} (ppm). The radiation trapping effect suggests that two different transition lines of Hg at 253.65 nm and 365.01 nm be selected for emission measurements in lower (<50 ppm) and higher concentration ranges (>50 ppm), respectively. In the CRDS mode, the detection limit of Hg in the metastable state 6s6p {sup 3}P{sub 0} is achieved to be 2.24 parts per 10{sup 12} (ppt) when the plasma is operating at 150 W with sample gas flow rate of 480 mL min{sup -1}; the detection limit corresponds to 50 ppm in Hg sample solution. Advantage of this novel spectrometer has two-fold, it has a large measurement dynamic range, from a few ppt to hundreds ppm and the CRDS mode can serve as calibration for the OES mode as well as high sensitivity measurements. Measurements of seven other elements, As, Cd, Mn, Ni, P, Pb, and Sr, using the OES mode are also carried out with detection limits of 1100, 33, 30, 144, 576, 94, and 2 ppb, respectively. Matrix effect in the presence of other elements on Hg measurements has been found to increase the detection limit to 131 ppb. These elements in lower concentrations can also be measured in the CRDS mode when a compact laser source is available to be integrated into the spectrometer in the future. This exploratory study demonstrates a new instrument platform using an OES-CRDS dual-mode technique for potential field applications.

Sahay, Peeyush; Scherrer, Susan T.; Wang Chuji [Department of Physics and Astronomy, Mississippi State University, Starkville, Mississippi 39759 (United States)

2012-09-15T23:59:59.000Z

133

It's Elemental - Isotopes of the Element Phosphorus  

NLE Websites -- All DOE Office Websites (Extended Search)

Silicon Silicon Previous Element (Silicon) The Periodic Table of Elements Next Element (Sulfur) Sulfur Isotopes of the Element Phosphorus [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 31 100% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 24 No Data Available Electron Capture (suspected) No Data Available Proton Emission (suspected) No Data Available 25 < 30 nanoseconds Proton Emission 100.00% 26 43.7 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission No Data Available 27 260 milliseconds Electron Capture 100.00% Electron Capture with

134

Trifluoromethyl Sulfur Pentafluoride (SF5CF3) and Sulfur Hexafluoride...  

NLE Websites -- All DOE Office Websites (Extended Search)

Sulfur Pentafluoride (SF5CF3) and Sulfur Hexafluoride (SF6) from Dome Concordia graphics Graphics data Data Investigators W. T. Sturges,1 T. J. Wallington,2 M. D. Hurley,2 K....

135

Production of elemental sulfur and methane from H{sub 2}S and CO{sub 2} derived from a coal desulfurization process. Quarterly technical progress report, October 1, 1995--December 31, 1995  

DOE Green Energy (OSTI)

During the ninth quarter of the project, bench scale experiments were performed to investigate the adsorption ability of different kinds of materials within sulfur vapor environment. Four kinds of adsorbents have been tested. The experiment results indicated that activated carbon was the best of four adsorbents tested. The adsorption process may be applicable to promote conversion of H{sub 2}S in the H{sub 2}S and SO{sub 2} reaction system.

Gong, S.-Y.; Jiang, X.; Khang, S.-J.; Keener, T.C.

1995-12-31T23:59:59.000Z

136

Sodium sulfur battery seal  

DOE Patents (OSTI)

This disclosure is directed to an improvement in a sodium sulfur battery construction in which a seal between various battery compartments is made by a structure in which a soft metal seal member is held in a sealing position by holding structure. A pressure applying structure is used to apply pressure on the soft metal seal member when it is being held in sealing relationship to a surface of a container member of the sodium sulfur battery by the holding structure. The improvement comprises including a thin, well-adhered, soft metal layer on the surface of the container member of the sodium sulfur battery to which the soft metal seal member is to be bonded.

Mikkor, Mati (Ann Arbor, MI)

1981-01-01T23:59:59.000Z

137

Mercury and Other Trace Metals in Coal  

Science Conference Proceedings (OSTI)

This document summarizes the trace metal analyses of more than 150 as-received bituminous, sub-bituminous, and lignite coal samples from full-scale power plants. Analyses for mercury, arsenic, beryllium, cadmium, chromium, copper, nickel, and lead offer a benchmark for utilities to compare and contrast their own estimates and measurements of trace element content in coal.

1997-02-25T23:59:59.000Z

138

A Soft Approach to Encapsulate Sulfur: Polyaniline Nanotubes for Lithium-Sulfur Batteries with Long Cycle Life  

SciTech Connect

Applications of rechargeable batteries are diverse and range from storing energy from renewable resources such as wind generators and solar arrays , powering electric vehicles and portable electronic devices. Significant R&D efforts have focused on achieving high energy density, long cycling life, low cost, and safety.1 Among all known rechargeable battery systems, lithium-sulfur (Li-S) batteries have attracted considerable attention.2, 3 Elemental sulfur is abundant, and is a very attractive cathode material for lithium batteries because of its high theoretical capacity (1672 mAh g-1) and specific energy (2600 Wh kg-1), assuming complete reaction of lithium with sulfur to form Li2S.

Xiao, Lifen; Cao, Yuliang; Xiao, Jie; Schwenzer, Birgit; Engelhard, Mark H.; Saraf, Laxmikant V.; Nie, Zimin; Exarhos, Gregory J.; Liu, Jun

2012-03-02T23:59:59.000Z

139

Low Quality Natural Gas Sulfur Removal and Recovery CNG Claus Sulfur Recovery Process  

Science Conference Proceedings (OSTI)

Increased use of natural gas (methane) in the domestic energy market will force the development of large non-producing gas reserves now considered to be low quality. Large reserves of low quality natural gas (LQNG) contaminated with hydrogen sulfide (H{sub 2}S), carbon dioxide (CO{sub 2}) and nitrogen (N) are available but not suitable for treatment using current conventional gas treating methods due to economic and environmental constraints. A group of three technologies have been integrated to allow for processing of these LQNG reserves; the Controlled Freeze Zone (CFZ) process for hydrocarbon / acid gas separation; the Triple Point Crystallizer (TPC) process for H{sub 2}S / C0{sub 2} separation and the CNG Claus process for recovery of elemental sulfur from H{sub 2}S. The combined CFZ/TPC/CNG Claus group of processes is one program aimed at developing an alternative gas treating technology which is both economically and environmentally suitable for developing these low quality natural gas reserves. The CFZ/TPC/CNG Claus process is capable of treating low quality natural gas containing >10% C0{sub 2} and measurable levels of H{sub 2}S and N{sub 2} to pipeline specifications. The integrated CFZ / CNG Claus Process or the stand-alone CNG Claus Process has a number of attractive features for treating LQNG. The processes are capable of treating raw gas with a variety of trace contaminant components. The processes can also accommodate large changes in raw gas composition and flow rates. The combined processes are capable of achieving virtually undetectable levels of H{sub 2}S and significantly less than 2% CO in the product methane. The separation processes operate at pressure and deliver a high pressure (ca. 100 psia) acid gas (H{sub 2}S) stream for processing in the CNG Claus unit. This allows for substantial reductions in plant vessel size as compared to conventional Claus / Tail gas treating technologies. A close integration of the components of the CNG Claus process also allow for use of the methane/H{sub 2}S separation unit as a Claus tail gas treating unit by recycling the CNG Claus tail gas stream. This allows for virtually 100 percent sulfur recovery efficiency (virtually zero SO{sub 2} emissions) by recycling the sulfur laden tail gas to extinction. The use of the tail gas recycle scheme also deemphasizes the conventional requirement in Claus units to have high unit conversion efficiency and thereby make the operation much less affected by process upsets and feed gas composition changes. The development of these technologies has been ongoing for many years and both the CFZ and the TPC processes have been demonstrated at large pilot plant scales. On the other hand, prior to this project, the CNG Claus process had not been proven at any scale. Therefore, the primary objective of this portion of the program was to design, build and operate a pilot scale CNG Claus unit and demonstrate the required fundamental reaction chemistry and also demonstrate the viability of a reasonably sized working unit.

Klint, V.W.; Dale, P.R.; Stephenson, C.

1997-10-01T23:59:59.000Z

140

Why sequence Alkaliphilic sulfur oxidizing bacteria for sulfur pollution  

NLE Websites -- All DOE Office Websites (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

Note: This page contains sample records for the topic "trace elements 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

It's Elemental - The Element Iodine  

NLE Websites -- All DOE Office Websites (Extended Search)

Tellurium Tellurium Previous Element (Tellurium) The Periodic Table of Elements Next Element (Xenon) Xenon The Element Iodine [Click for Isotope Data] 53 I Iodine 126.90447 Atomic Number: 53 Atomic Weight: 126.90447 Melting Point: 386.85 K (113.7°C or 236.7°F) Boiling Point: 457.55 K (184.4°C or 364.0°F) Density: 4.93 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Non-metal Period Number: 5 Group Number: 17 Group Name: Halogen What's in a name? From the Greek word for violet, iodes. Say what? Iodine is pronounced as EYE-eh-dine or as EYE-eh-din. History and Uses: Iodine was discovered by the French chemist Barnard Courtois in 1811. Courtois was extracting sodium and potassium compounds from seaweed ash. Once these compounds were removed, he added sulfuric acid (H2SO4) to

142

Formulated 2-Traces - CECM  

E-Print Network (OSTI)

Nov 19, 1997 ... next up previous. Next: Characteristics of truth tables Up: Introduction to Traces Previous: Definition of the n-Trace...

143

Trace elements in the aluminum value chain  

Science Conference Proceedings (OSTI)

Retrofit of a Combined Breaker Feeder with a Chisel Bath Contact Detection System to Reduce Anode Effect Frequency in a Potroom Simulating Traffic in a...

144

Trace elements and Polycyclic Aromatic Hydrocarbons (PAHs)  

E-Print Network (OSTI)

.2.2 Anthropogenic emissions 28 2.3 Polycyclic Aromatic Hydrocarbons 30 2.3.1 Sources of PAHs 30 2.3.2 Gas to particle distribution in atmosphere 32 2.3.3 Gas to particle distribution in atmosphere 32 CHAPTER THREE

Paris-Sud XI, Université de

145

Trace Element Analysis Core Lab methods  

E-Print Network (OSTI)

), Hg and Pb (no gas mode). Selenium and Fe are analysed in collision mode with H2. The sample strem a weighed sample is placed in either a 15 ml or 50 ml centrifuge tube and an appropriate volume of optima analysis is performed in the 15 ml centrifuge tubes with addition of 0.5 mls HNO3. For sediment/soils 0

Lotko, William

146

DEPOSITION OF TOXIC TRACE ELEMENTS AND HEAVY ...  

Science Conference Proceedings (OSTI)

... on sub-micrometer (ie, fine) particles was emitted from oil-fired power plants. Likewise, sele- nium is a marker of coal combustion particles; Zn ...

1999-06-25T23:59:59.000Z

147

Sulfur recovery in U.S. refineries is at an all-time high  

SciTech Connect

Environmental pressures are reducing allowable sulfur emissions and tightening fuel sulfur specifications on a global basis. Combined with an increasingly sour crude slate, this means that ever-greater quantities of sulfur are recovered each year. Sulfur is produced through three main routes: Frasch mining, recovery from pyrites, and recovery from crude oil and natural gas. Sulfur recovery from US refineries reached an all-time high in 1995: 13,753 metric tons/calendar day (mt/cd). Frasch mining has lost its place as the primary source of elemental sulfur. Current demand patterns for sulfur are expected to continue through the next decade. About half of world sulfur production will be used to produce phosphatic fertilizers. The other half will be used in some 30 chemically oriented industries. The data reported in this article were collected by the US Bureau of Mines/US Geological Survey, unless otherwise noted. The paper discusses sulfur from natural gas, sulfur from refineries, sulfur prices, imports and exports.

Swain, E.J. [Swain (Edward J.), Houston, TX (United States)

1997-04-21T23:59:59.000Z

148

Production of elemental sulfur and methane from H{sub 2}S and CO{sub 2} derived from a coal desulfurization process. Quarterly technical progress report, January 1--March 31, 1996  

DOE Green Energy (OSTI)

During the tenth quarter of the project, bench scale experiments were performed to investigate the adsorption ability of different kinds of materials within sulfur vapor environment. Four kinds of adsorbents have been tested. The experimental results indicated that activated carbon was the best of four adsorbents tested. In addition to the baseline tests, several designs of activated carbon feed system have been tested. Under an inert environment, bench scale experiments were performed to investigate the characteristics and efficiency of activated carbon passing through the Co-Mo-Alumina catalyst bed. The results showed that activated carbon powder could easily be transported through the catalytic bed. The adsorption process may be applicable to promote conversion of H{sub 2}S in the H{sub 2}S and CO{sub 2} reaction system.

Gong, S.Y.; Jiang, X.; Khang, S.J.; Keener, T.C.

1996-12-31T23:59:59.000Z

149

Why sequence purple sulfur bacteria?  

NLE Websites -- All DOE Office Websites (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

150

Process for removing sulfur from sulfur-containing gases  

DOE Patents (OSTI)

The present disclosure relates to improved processes for treating hot sulfur-containing flue gas to remove sulfur therefrom. Processes in accorda The government may own certain rights in the present invention pursuant to EPA Cooperative Agreement CR 81-1531.

Rochelle, Gary T. (Austin, TX); Jozewicz, Wojciech (Chapel Hill, NC)

1989-01-01T23:59:59.000Z

151

Characterization of a transient +2 sulfur oxidation state intermediate from the oxidation of aqueous sulfide  

Science Conference Proceedings (OSTI)

The oxidation H{sub 2}S to sulfate involves a net transfer of eight electrons and occurs through the formation of several partially oxidized intermediates with oxidation states ranging from {minus}1 to +5. Known intermediates include elemental sulfur (oxidation state 0), polysulfides (outer sulfur: {minus}1, inner sulfur: 0), sulfite (+4) and thiosulfate (outer sulfur: {minus}1, inner sulfur: +5). A noticeable gap in this series of intermediates is that of a +2 sulfur oxidation state oxoacid/oxoanion species, which was never detected experimentally. Here, we present evidence of the transient existence of +2 oxidation state intermediate in the Ni(II)-catalyzed oxidation of aqueous sulfide. X-ray absorption near-edge structure (XANES) spectroscopy and Fourier-transform-infrared (FT-IR) spectroscopy were used to characterize this species; they suggest that it has a sulfoxylate ion (SO{sub 2}{sup 2{minus}}) structure.

Vairavmurthy, M.A.; Zhou, Weiqing

1995-04-01T23:59:59.000Z

152

Production of elemental sulfur from H{sub 2}S and CO{sub 2} derived from a coal desulfurization process. Quarterly technical process report, April 1, 1994--June 30, 1994  

SciTech Connect

During the third quarter of this project, by using the apparatus previously setup for preparation of catalysts, the CoO-MoO{sub 3}-Al{sub 2}O{sub 3} catalyst was prepared and the thermal stability of the catalyst was tested. Efforts were made on the calibration and the programming of the two column GC of a Perkin Elmer Gas Chromatograph. Column A was used for detecting sulfur related substances such as H{sub 2}S, COS and CS{sub 2}, and column B was for CO, CH{sub 4} and H{sub 2}. All of the GC standard curves were obtained. Non-catalytic experiments were carried out by using the packed bed reactor system with blank, filled only with quartz wool and Al{sub 2}O{sub 3} support for future reference. A modified new reactor was designed to quickly quench the reaction and to prohibit the occurrence of re-equilibration of reaction products. Further thermodynamic analyses for the reaction of H{sub 2}S and CO, were performed using the Stanjan method.

Hu, Longsheng; Jiang, Xueyu; Khang, Soon-Jai

1994-08-01T23:59:59.000Z

153

Volume efficient sodium sulfur battery  

SciTech Connect

In accordance with the teachings of this specification, a sodium sulfur battery is formed as follows. A plurality of box shaped sulfur electrodes are provided, the outer surfaces of which are defined by an electrolyte material. Each of the electrodes have length and width dimensions substantially greater than the thicknesses thereof as well as upwardly facing surface and a downwardly facing surface. An electrode structure is contained in each of the sulfur electrodes. A holding structure is provided for holding the plurality of sulfur electrodes in a stacked condition with the upwardly facing surface of one sulfur electrode in facing relationship to the downwardly facing surface of another sulfur electrode thereabove. A small thickness dimension separates each of the stacked electrodes thereby defining between each pair of sulfur electrodes a volume which receives the sodium reactant. A reservoir is provided for containing sodium. A manifold structure interconnects the volumes between the sulfur electrodes and the reservoir. A metering structure controls the flow of sodium between the reservoir and the manifold structure.

Mikkor, Mati (Ann Arbor, MI)

1980-01-01T23:59:59.000Z

154

Why Sequence Bacteria That Reduce Sulfur Compounds?  

NLE Websites -- All DOE Office Websites (Extended Search)

Bacteria That Reduce Sulfur Compounds? Combustion of sulfur-containing fuels, such as coal, oil, and natural gas, contributes significantly to global environmental problems, such...

155

Production of elemental sulfur and methane from H{sub 2}S and CO{sub 2} derived from a coal desulfurization process. Annual technical progress report, October 1, 1995--September 30, 1996; Quarterly technical progress report, July 1--September 30, 1996  

DOE Green Energy (OSTI)

This annual report summarizes the results of the project during the third year period. The purpose of this study was to develop an experimental and theoretical procedure to investigate the feasibility of producing elemental sulfur, carbon monoxide, hydrogen and possibly methane from hydrogen sulfide and carbon dioxide through catalytic reactions. A standard experimental system that can evaluate potential catalysts under controlled laboratory conditions has been designed and constructed. And an effective simulation program capable of providing valuable thermodynamic information on the reaction system has been compiled. During this project year, the modified experimental system for the catalytic reaction studies was installed and the temperature distribution profile inside the reactor has been characterized. New flowmeters were replaced in the reaction system and calibrated to control the flowrates of H{sub 2}S, CO{sub 2}, H{sub 2} and N{sub 2}. Based on the experimental results of H{sub 2}S decomposition under both non-catalytic and catalytic conditions, bench scale experiments were performed with the CoO-MoO{sub 3}-Alumina catalyst at moderate temperatures, around 550 C, to investigate the adsorption effects using solid sorbents within a sulfur vapor environment. Four kinds of adsorbents have been tested. In addition to the above baseline tests, several designs of solid adsorbent feed system have been tested. Under both an inert and a real reaction environment, bench scale experiments were performed to investigate the characteristics and efficiency of activated carbon passing through the CoO-MoO{sub 3}-Alumina catalyst bed.

Jiang, X.; Khang, S.J.; Keener, T.C.

1996-12-31T23:59:59.000Z

156

Hydrogen and sulfur recovery from hydrogen sulfide wastes  

DOE Patents (OSTI)

A process is described for generating hydrogen and elemental sulfur from hydrogen sulfide waste in which the hydrogen sulfide is [dis]associated under plasma conditions and a portion of the hydrogen output is used in a catalytic reduction unit to convert sulfur-containing impurities to hydrogen sulfide for recycle, the process also including the addition of an ionizing gas such as argon to initiate the plasma reaction at lower energy, a preheater for the input to the reactor and an internal adjustable choke in the reactor for enhanced coupling with the microwave energy input.

Harkness, J.B.L.; Gorski, A.J.; Daniels, E.J.

1993-05-18T23:59:59.000Z

157

Hydrogen and sulfur recovery from hydrogen sulfide wastes  

DOE Patents (OSTI)

A process for generating hydrogen and elemental sulfur from hydrogen sulfide waste in which the hydrogen sulfide is associated under plasma conditions and a portion of the hydrogen output is used in a catalytic reduction unit to convert sulfur-containing impurities to hydrogen sulfide for recycle, the process also including the addition of an ionizing gas such as argon to initiate the plasma reaction at lower energy, a preheater for the input to the reactor and an internal adjustable choke in the reactor for enhanced coupling with the microwave energy input.

Harkness, John B. L. (Naperville, IL); Gorski, Anthony J. (Woodridge, IL); Daniels, Edward J. (Oak Lawn, IL)

1993-01-01T23:59:59.000Z

158

The Chemical Elements  

Science Conference Proceedings (OSTI)

Table 1   Names and symbols for the elements (in alphabetical order)...Sodium (j) Na Strontium Sr Sulfur S Tantalum Ta Technetium Tc Tellurium Te Terbium Tb Thallium Tl Thorium Th Thulium Tm Tin (k) Sn Titanium Ti Tungsten (l) W Ununnilium Uun Unununium Uuu Uranium U Vanadium V Xenon Xe Ytterbium Yb Yttrium Y Zinc Zn Zirconium Zr (a) Symbol based on the Latin

159

CE IGCC Repowering plant sulfuric acid plant. Topical report, June 1993  

SciTech Connect

A goal of the CE IGCC Repowering project is to demonstrate a hot gas clean-up system (HGCU), for the removal of sulfur from the product gas stream exiting the gasifier island. Combustion Engineering, Inc. (ABB CE) intends to use a HGCU developed by General Electric Environmental Services (GEESI). The original design of this system called for the installation of the HGCU, with a conventional cold gas clean-up system included as a full-load operational back-up. Each of these systems removes sulfur compounds and converts them into an acid off-gas. This report deals with the investigation of equipment to treat this off-gas, recovering these sulfur compounds as elemental sulfur, sulfuric acid or some other form. ABB CE contracted ABB Lummus Crest Inc. (ABB LCI) to perform an engineering evaluation to compare several such process options. This study concluded that the installation of a sulfuric acid plant represented the best option from both a technical and economic point of view. Based on this evaluation, ABB CE specified that a sulfuric acid plant be installed to remove sulfur from off-gas exiling the gas clean-up system. ABB LCI prepared a request for quotation (RFQ) for the construction of a sulfuric acid production plant. Monsanto Enviro-Chem Inc. presented the only proposal, and was eventually selected as the EPC contractor for this system.

Chester, A.M.

1993-12-01T23:59:59.000Z

160

CGC Trace Species Partitioning  

NLE Websites -- All DOE Office Websites (Extended Search)

per square inch gage Sb Antimony scfd Standard cubic feet per day Se Selenium SO 2 SOFC Solid oxide fuel cell Sulfur dioxide V Vanadium vol% Volume percent Zn Zinc C Degrees...

Note: This page contains sample records for the topic "trace elements 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

Halocarbon and Other Atmospheric Trace Species (HATS) | Data.gov  

NLE Websites -- All DOE Office Websites (Extended Search)

Halocarbon and Other Atmospheric Trace Species (HATS) Halocarbon and Other Atmospheric Trace Species (HATS) Agriculture Community Menu DATA APPS EVENTS DEVELOPER STATISTICS COLLABORATE ABOUT Agriculture You are here Data.gov » Communities » Agriculture » Data Halocarbon and Other Atmospheric Trace Species (HATS) Dataset Summary Description The general mission of the Halocarbons and other Atmospheric Trace Species group is to quantify the distributions and magnitudes of sources and sinks for atmospheric nitrous oxide (N2O) and halogen containing compounds. HATS utilizes numerous types of platforms, including ground-based stations, towers, ocean vessels, aircraft, and balloons, to accomplish its mission. For a detailed mission statement, consult our FAQ. Tags {"nitrous oxide","sulfur hexaflouride",CFC-11,CFC-12,CFC-113,CCl4,CH3CCl3,CH3Cl,halon-1211,HCFC-22,HCFC-142b,halocarbons,chromatograph,aircraft,balloons,vessels,ships,towers,"natural resources",environment,air,"GHG "}

162

Alkali metal/sulfur battery  

SciTech Connect

Alkali metal/sulfur batteries in which the electrolyte-separator is a relatively fragile membrane are improved by providing means for separating the molten sulfur/sulfide catholyte from contact with the membrane prior to cooling the cell to temperatures at which the catholyte will solidify. If the catholyte is permitted to solidify while in contact with the membrane, the latter may be damaged. The improvement permits such batteries to be prefilled with catholyte and shipped, at ordinary temperatures.

Anand, Joginder N. (Clayton, CA)

1978-01-01T23:59:59.000Z

163

Nuclear elements in Banach Jordan pairs Ottmar Loos  

E-Print Network (OSTI)

Nuclear elements in Banach Jordan pairs Ottmar Loos Abstract We introduce nuclear elements in Banach Jordan pairs, generalizing the nuclear elements Jordan pairs and show that the trace form Trintroduced in [3] may be extended to the nuclear

164

Trace Metals Determination in Flue Gas Desulfurization Water  

Science Conference Proceedings (OSTI)

Flue gas desulfurization (FGD) scrubbers are used on coal-fired power plants to reduce sulfur dioxide emissions to air. While effective for this purpose, wet FGD scrubbers produce an aqueous blowdown stream that contains trace levels of metals adsorbed from flue gas. Power plant owners need to measure concentrations of these metals for purposes of process control, discharge monitoring, or design and operation of wastewater treatment systems. FGD water has proven to be a very difficult matrix to analyze a...

2009-12-28T23:59:59.000Z

165

Contamination of ground and surface waters due to uranium mining and milling. Volume I: Biological processes for concentrating trace elements from uranium mine waters. Open file report 25 Jul 79-14 Sep 81  

Science Conference Proceedings (OSTI)

Wastewater from uranium mines in the Ambrosia Lake district near Grants, N. Mex., contains uranium, selenium, radium, and molybdenum. A novel treatment process for waters from two mines, sections 35 and 36, to reduce the concentrations of the trace contaminants was developed. Particulates are settled by ponding and the waters are passed through an ion exchange resin to remove uranium; barium chloride is added to precipitate sulfate and radium from the mine waters. The mine waters are subsequently passed through three consecutive algae ponds prior to discharge. Water, sediment, and biological samples were collected over a 4-year period and analyzed to assess the role of biological agents in removal of inorganic trace contaminants from the mine waters.

Brieley, C.L.; Brierley, J.A.

1981-11-01T23:59:59.000Z

166

Assessing Potential Acidification of Marine Archaeological Wood Based on Concentration of Sulfur Species  

DOE Green Energy (OSTI)

The presence of sulfur in marine archaeological wood presents a challenge to conservation. Upon exposure to oxygen, sulfur compounds in waterlogged wooden artifacts are being oxidized, producing sulfuric acid. This speeds the degradation of the wood, potentially damaging specimens beyond repair. Sulfur K-edge x-ray absorption spectroscopy was used to identify the species of sulfur present in samples from the timbers of the Mary Rose, a preserved 16th century warship known to undergo degradation through acidification. The results presented here show that sulfur content varied significantly on a local scale. Only certain species of sulfur have the potential to produce sulfuric acid by contact with oxygen and seawater in situ, such as iron sulfides and elemental sulfur. Organic sulfurs, such as the amino acids cysteine and methionine, may produce acid but are integral parts of the wood's structure and may not be released from the organic matrix. The sulfur species contained in the sample reflect the exposure to oxygen while submerged, and this exposure can differ greatly over time and position. A better understanding of the species pathway to acidifications required, along with its location, in order to suggest a more customized and effective preservation strategy. Waterlogged archaeological wood, frequently in the form of shipwrecks, is being excavated for historical purposes in many countries around the world. Even after extensive efforts towards preservation, scientists are discovering that accumulation of sulfate salts results in acidic conditions on the surfaces of the artifacts. Sulfuric acid degrades structural fibers in the wood by acid hydrolysis of cellulose, accelerating the decomposition of the ship timbers. Determining the sulfur content of waterlogged wood is now of great importance in maritime archaeology. Artifact preservation is often more time consuming and expensive than the original excavation; but it is key to the availability of objects for future study as well as maintaining the integrity of historical data and preserving the value of museum pieces. Sulfur occurs in a wide number of oxidation states from -2 to +6, and appears in numerous organic and inorganic compounds in nature. However, it is a very minor component of wood. Sulfur K-edge x-ray absorption spectroscopy (XAS) is a valuable technique because it has the ability to detect very low concentrations of sulfur in the specimen. XAS is also sensitive to differences in oxidation states, as well as long and short range order in molecules.

Not Available

2011-06-22T23:59:59.000Z

167

Introduction to Traces - CECM  

E-Print Network (OSTI)

Nov 19, 1997 ... Section 2 describes patterns that arise in the construction of truth tables for traces and their theoretical interest for the completeness problem.

168

High-temperature sorbent method for removal of sulfur containing gases from gaseous mixtures  

DOE Patents (OSTI)

A copper oxide-zinc oxide mixture is used as a sorbent for removing hydrogen sulfide and other sulfur containing gases at high temperatures from a gaseous fuel mixture. This high-temperature sorbent is especially useful for preparing fuel gases for high temperature fuel cells. The copper oxide is initially reduced in a preconditioning step to elemental copper and is present in a highly dispersed state throughout the zinc oxide which serves as a support as well as adding to the sulfur sorption capacity. The spent sorbent is regenerated by high-temperature treatment with an air fuel, air steam mixture followed by hydrogen reduction to remove and recover the sulfur.

Young, J.E.; Jalan, V.M.

1984-06-19T23:59:59.000Z

169

High-temperature sorbent method for removal of sulfur containing gases from gaseous mixtures  

DOE Patents (OSTI)

A copper oxide-zinc oxide mixture is used as a sorbent for removing hydrogen sulfide and other sulfur containing gases at high temperatures from a gaseous fuel mixture. This high-temperature sorbent is especially useful for preparing fuel gases for high temperature fuel cells. The copper oxide is initially reduced in a preconditioning step to elemental copper and is present in a highly dispersed state throughout the zinc oxide which serves as a support as well as adding to the sulfur sorption capacity. The spent sorbent is regenerated by high-temperature treatment with an air fuel, air steam mixture followed by hydrogen reduction to remove and recover the sulfur.

Young, John E. (Woodridge, IL); Jalan, Vinod M. (Concord, MA)

1984-01-01T23:59:59.000Z

170

GPU ray tracing  

Science Conference Proceedings (OSTI)

The NVIDIA OptiX ray tracing engine is a programmable system designed for NVIDIA GPUs and other highly parallel architectures. The OptiX engine builds on the key observation that most ray tracing algorithms can be implemented using a small ...

Steven G. Parker; Heiko Friedrich; David Luebke; Keith Morley; James Bigler; Jared Hoberock; David McAllister; Austin Robison; Andreas Dietrich; Greg Humphreys; Morgan McGuire; Martin Stich

2013-05-01T23:59:59.000Z

171

Ray tracing visualization toolkit  

Science Conference Proceedings (OSTI)

The Ray Tracing Visualization Toolkit (rtVTK) is a collection of programming and visualization tools supporting visual analysis of ray-based rendering algorithms. rtVTK leverages layered visualization within the spatial domain of computation, enabling ... Keywords: ray tracing, ray-based rendering, visualization

Christiaan Gribble; Jeremy Fisher; Daniel Eby; Ed Quigley; Gideon Ludwig

2012-03-01T23:59:59.000Z

172

Process for recovery of sulfur from acid gases  

DOE Patents (OSTI)

Elemental sulfur is recovered from the H.sub.2 S present in gases derived from fossil fuels by heating the H.sub.2 S with CO.sub.2 in a high-temperature reactor in the presence of a catalyst selected as one which enhances the thermal dissociation of H.sub.2 S to H.sub.2 and S.sub.2. The equilibrium of the thermal decomposition of H.sub.2 S is shifted by the equilibration of the water-gas-shift reaction so as to favor elemental sulfur formation. The primary products of the overall reaction are S.sub.2, CO, H.sub.2 and H.sub.2 O. Small amounts of COS, SO.sub.2 and CS.sub.2 may also form. Rapid quenching of the reaction mixture results in a substantial increase in the efficiency of the conversion of H.sub.2 S to elemental sulfur. Plant economy is further advanced by treating the product gases to remove byproduct carbonyl sulfide by hydrolysis, which converts the COS back to CO.sub.2 and H.sub.2 S. Unreacted CO.sub.2 and H.sub.2 S are removed from the product gas and recycled to the reactor, leaving a gas consisting chiefly of H.sub.2 and CO, which has value either as a fuel or as a chemical feedstock and recovers the hydrogen value from the H.sub.2 S.

Towler, Gavin P. (Kirkbymoorside, GB2); Lynn, Scott (Pleasant Hill, CA)

1995-01-01T23:59:59.000Z

173

Oxidation of hydrogen halides to elemental halogens  

DOE Patents (OSTI)

A process for oxidizing hydrogen halides having substantially no sulfur impurities by means of a catalytically active molten salt is disclosed. A mixture of the subject hydrogen halide and an oxygen bearing gas is contacted with a molten salt containing an oxidizing catalyst and alkali metal normal sulfates and pyrosulfates to produce an effluent gas stream rich in the elemental halogen and substantially free of sulfur oxide gases.

Rohrmann, Charles A. (Kennewick, WA); Fullam, Harold T. (Richland, WA)

1985-01-01T23:59:59.000Z

174

Ultra-Low Sulfur Diesel Fuel | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Ultra-Low Sulfur Diesel Fuel Ultra-Low Sulfur Diesel Fuel August 20, 2013 - 8:53am Addthis Ultra-low sulfur diesel (ULSD) is diesel fuel with 15 parts per million or lower sulfur...

175

Energy Basics: Ultra-Low Sulfur Diesel Fuel  

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

Hydrogen Natural Gas Propane Ultra-Low Sulfur Diesel Vehicles Ultra-Low Sulfur Diesel Fuel Ultra-low sulfur diesel (ULSD) is diesel fuel with 15 parts per million or lower sulfur...

176

Ultra-Low Sulfur Diesel Fuel  

Energy.gov (U.S. Department of Energy (DOE))

Ultra-low sulfur diesel (ULSD) is diesel fuel with 15 parts per million or lower sulfur content. The U.S. Environmental Protection Agency requires 80% of the highway diesel fuel refined in or...

177

It's Elemental - The Element Fermium  

NLE Websites -- All DOE Office Websites (Extended Search)

Einsteinium Previous Element (Einsteinium) The Periodic Table of Elements Next Element (Mendelevium) Mendelevium The Element Fermium Click for Isotope Data 100 Fm Fermium 257...

178

It's Elemental - The Element Neptunium  

NLE Websites -- All DOE Office Websites (Extended Search)

Uranium Previous Element (Uranium) The Periodic Table of Elements Next Element (Plutonium) Plutonium The Element Neptunium Click for Isotope Data 93 Np Neptunium 237 Atomic...

179

It's Elemental - The Element Ruthenium  

NLE Websites -- All DOE Office Websites (Extended Search)

Technetium Previous Element (Technetium) The Periodic Table of Elements Next Element (Rhodium) Rhodium The Element Ruthenium Click for Isotope Data 44 Ru Ruthenium 101.07 Atomic...

180

It's Elemental - The Element Actinium  

NLE Websites -- All DOE Office Websites (Extended Search)

Radium Previous Element (Radium) The Periodic Table of Elements Next Element (Thorium) Thorium The Element Actinium Click for Isotope Data 89 Ac Actinium 227 Atomic Number: 89...

Note: This page contains sample records for the topic "trace elements 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

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 10 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, W.E.

1991-12-31T23:59:59.000Z

182

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

183

THE SOLAR FLARE SULFUR ABUNDANCE FROM RESIK OBSERVATIONS  

SciTech Connect

The RESIK instrument on CORONAS-F spacecraft observed several sulfur X-ray lines in three of its four channels covering the wavelength range 3.8-6.1 A during solar flares. The fluxes are analyzed to give the sulfur abundance. Data are chosen for when the instrument parameters were optimized. The measured fluxes of the S XV 1s{sup 2}-1s4p (w4) line at 4.089 A gives A(S) = 7.16 {+-} 0.17 (abundances on a logarithmic scale with A(H) = 12) which we consider to be the most reliable. Estimates from other lines range from 7.13 to 7.24. The preferred S abundance estimate is very close to recent photospheric abundance estimates and to quiet-Sun solar wind and meteoritic abundances. This implies no fractionation of sulfur by processes tending to enhance the coronal abundance from the photospheric that depend on the first ionization potential (FIP), or that sulfur, though its FIP has an intermediate value of 10.36 eV, acts like a 'high-FIP' element.

Sylwester, J.; Sylwester, B. [Space Research Centre, Polish Academy of Sciences, 51-622, Kopernika 11, Wroclaw (Poland); Phillips, K. J. H. [Mullard Space Science Laboratory, University College London, Holmbury St. Mary, Dorking, Surrey RH5 6NT (United Kingdom); Kuznetsov, V. D., E-mail: js@cbk.pan.wroc.pl, E-mail: bs@cbk.pan.wroc.pl, E-mail: kjhp@mssl.ucl.ac.uk, E-mail: kvd@izmiran.ru [Institute of Terrestrial Magnetism and Radiowave Propagation (IZMIRAN), Troitsk, Moscow (Russian Federation)

2012-06-01T23:59:59.000Z

184

Seal for sodium sulfur battery  

SciTech Connect

This invention is directed to a seal for a sodium sulfur battery in which the sealing is accomplished by a radial compression seal made on a ceramic component of the battery which separates an anode compartment from a cathode compartment of the battery.

Topouzian, Armenag (Birmingham, MI); Minck, Robert W. (Lathrup Village, MI); Williams, William J. (Northville, MI)

1980-01-01T23:59:59.000Z

185

Sensor Data Trace Communication  

This is a method and process for detecting, locating and quantifying physical phenomena using a data trace that may be incorporated and/or installed on structures including oil and gas pipes and bridges, buildings, etc.

186

Process for reducing sulfur in coal char  

DOE Patents (OSTI)

Coal is gasified in the presence of a small but effective amount of alkaline earth oxide, hydroxide or carbonate to yield a char fraction depleted in sulfur. Gases produced during the reaction are enriched in sulfur compounds and the alkaline earth compound remains in the char fraction as an alkaline earth oxide. The char is suitable for fuel use, as in a power plant, and during combustion of the char the alkaline earth oxide reacts with at least a portion of the sulfur oxides produced from the residual sulfur contained in the char to further lower the sulfur content of the combustion gases.

Gasior, Stanley J. (Pittsburgh, PA); Forney, Albert J. (Coraopolis, PA); Haynes, William P. (Pittsburgh, PA); Kenny, Richard F. (Venetia, PA)

1976-07-20T23:59:59.000Z

187

Preparation of Building Material Using Elemental Sulfur and Heavy ...  

Science Conference Proceedings (OSTI)

Furthermore, when NaOH is applied as an additive in the process of ... Effect of Processes in Degraded Decoloration of Frying Oil Treated with Brazilian Clays ... Novel Technology for Wastewater Treatment by Biologics in Hydrometallurgical ... Study on the EMD Residue and Shale for Preparing Solidification Brick.

188

Removal of Elemental Sulfur from Hydrometallurgical Waste Derived ...  

Science Conference Proceedings (OSTI)

Selective Recovery of Gold from E-wastes by Using Cellulosic Wastes Stabilization of Chromium-Based Slags with FeS2 and FeSO4 Sulphide Precipitation...

189

It's Elemental - The Element Calcium  

NLE Websites -- All DOE Office Websites (Extended Search)

little demand for metallic calcium. It is used in some chemical processes to refine thorium, uranium and zirconium. Calcium is also used to remove oxygen, sulfur and carbon from...

190

Element associations in ash from waste combustion in fluidized bed  

SciTech Connect

The incineration of MSW in fluidized beds is a commonly applied waste management practice. The composition of the ashes produced in a fluidized bed boiler has important environmental implications as potentially toxic trace elements may be associated with ash particles and it is therefore essential to determine the mechanisms controlling the association of trace elements to ash particles, including the role of major element composition. The research presented here uses micro-analytical techniques to study the distribution of major and trace elements and determine the importance of affinity-based binding mechanisms in separate cyclone ash particles from MSW combustion. Particle size and the occurrence of Ca and Fe were found to be important factors for the binding of trace elements to ash particles, but the binding largely depends on random associations based on the presence of a particle when trace elements condensate in the flue gas.

Karlfeldt Fedje, K., E-mail: karinka@chalmers.s [Department of Chemical and Biological Engineering, Division of Environmental Inorganic Chemistry, Chalmers University of Technology, Kemivaegen 10, 412 96 Goeteborg (Sweden); Rauch, S. [Department of Civil and Environmental Engineering, Division of Water Environment Technology, Chalmers University of Technology, Sven Hultins Gata 8, 412 96 Goeteborg (Sweden); Cho, P.; Steenari, B.-M. [Department of Chemical and Biological Engineering, Division of Environmental Inorganic Chemistry, Chalmers University of Technology, Kemivaegen 10, 412 96 Goeteborg (Sweden)

2010-07-15T23:59:59.000Z

191

Received: 21 November 2010 Revised: 5 January 2011 Accepted: 5 January 2011 Published online in Wiley Online Library: 2011 Spatial distributions of carbon, nitrogen and sulfur isotope  

E-Print Network (OSTI)

in Wiley Online Library: 2011 Spatial distributions of carbon, nitrogen and sulfur isotope ratios in human, Salt Lake City, UT 84108, USA 3 Department of Geology and Geophysics, University of Utah, 135 South) and sulfur (d34 S) isotope ratios of human hair collected in the central portions of the USA. These elements

Ehleringer, Jim

192

World petroleum-derived sulfur production  

SciTech Connect

Research efforts in new uses for sulfur, among them those of the Sulfur Development Institute of Canada, have resulted in the development of several new product markets. Petroleum and natural gas derived sulfurs are finding use as asphalt extenders in road construction throughout North America and as concrete extenders and substitutes for Portland cement in the construction industries of Mexico and the Middle East. Their use in masonry blocks is now being commercialized. Canada is the world's largest producer of commercial sulfur; 80% of it is used as a processing chemical in the form of sulfuric acid. Saudi Arabia, recently having begun to commercialize its vast resources, is constructing plants for the extraction of sulfur from natural gas and plans to export between 6 and 7 x 10/sup 5/ tons annually, much of it for fertilizer manufacture to India, Tunisia, Italy, Pakistan, Greece, Morocco, and Thailand.

Cantrell, A.

1982-08-02T23:59:59.000Z

193

Topsoe`s Wet gas Sulfuric Acid (WSA) process: An alternative technology for recovering refinery sulfur  

SciTech Connect

The Topsoe Wet gas Sulfuric Acid (WSA) process is a catalytic process which produces concentrated sulfuric acid from refinery streams containing sulfur compounds such as H{sub 2}S (Claus plant feed), Claus plant tail gas, SO{sub 2} (FCC off-gas, power plants), and spent sulfuric acid (alkylation acid). The WSA process recovers up to 99.97% of the sulfur value in the stream as concentrated sulfuric acid (93--98.5 wt%). No solid waste products or waste water is produced and no chemicals are consumed in the process. The simple process layout provides low capital cost and attractive operating economy. Twenty four commercial WSA plants have been licensed. The WSA process is explained in detail and comparisons with alternative sulfur management technology are presented. Environmental regulations applying to SO{sub x} abatement and sulfuric acid production plants are explained in the context of WSA plant operation.

Ward, J.W. [Haldor Topsoe, Inc., Houston, TX (United States)

1995-09-01T23:59:59.000Z

194

HYDROCARBON AND SULFUR SENSORS FOR SOFC SYSTEMS  

DOE Green Energy (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

195

Trace Impurities and Activation Products in Base Metals  

Science Conference Proceedings (OSTI)

This report documents the results of research related to the concentrations of trace impurities and activation products in stainless steel alloys used for reactor vessels and internals. While present in extremely low concentrations, these trace elements and radionuclides can impact radioactive waste disposal of the components upon decommissioning.BackgroundThe primary basis of activity in a decommissioning source term is activated metals from the reactor and ...

2012-10-30T23:59:59.000Z

196

Improved sulfur removal processes evaluated for IGCC  

SciTech Connect

An inherent advantage of Integrated Coal Gasification Combined Cycle (IGCC) electric power generation is the ability to easily remove and recover sulfur. During the last several years, a number of new, improved sulfur removal and recovery processes have been commercialized. An assessment is given of alternative sulfur removal processes for IGCC based on the Texaco coal gasifier. The Selexol acid gas removal system, Claus sulfur recovery, and SCOT tail gas treating are currently used in Texaco-based IGCC. Other processes considered are: Purisol, Sulfinol-M, Selefning, 50% MDEA, Sulften, and LO-CAT. 2 tables.

1986-12-01T23:59:59.000Z

197

Retail Prices for Ultra Low Sulfur Diesel  

U.S. Energy Information Administration (EIA)

Beginning July 26, 2010 publication of Ultra Low Sulfur Diesel (ULSD) price became fully represented by the Diesel Average All Types price. As of December 1, ...

198

Natural Gas Processing Plant- Sulfur (New Mexico)  

Energy.gov (U.S. Department of Energy (DOE))

This regulation establishes sulfur emission standards for natural gas processing plants. Standards are stated for both existing and new plants. There are also rules for stack height requirements,...

199

Tracing Geothermal Fluids  

DOE Green Energy (OSTI)

Chemical compounds have been designed under this contract that can be used to trace water that has been injected into vapor-dominated and two-phase geothermal fields. Increased knowledge of the injection flow is provided by the tracers, and this augments the power that can be produced. Details on the stability and use of these tracers are included in this report.

Michael C. Adams Greg Nash

2004-03-31T23:59:59.000Z

200

Sulfur  

U.S. Energy Information Administration (EIA)

-No Data Reported; --= Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Notes: Hydrogen production ...

Note: This page contains sample records for the topic "trace elements 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

Design and operation of the coke-oven gas sulfur removal facility at Geneva Steel  

Science Conference Proceedings (OSTI)

The coke-oven gas sulfur removal facility at Geneva Steel utilizes a combination of two technologies which had never been used together. These two technologies had proven effective separately and now in combination. However, it brought unique operational considerations which has never been considered previously. The front end of the facility is a Sulfiban process. This monoethanolamine (MEA) process effectively absorbs hydrogen sulfide and other acid gases from coke-oven gas. The final step in sulfur removal uses a Lo-Cat II. The Lo-Cat process absorbs and subsequently oxidizes H{sub 2}S to elemental sulfur. These two processes have been effective in reducing sulfur dioxide emissions from coke-oven gas by 95%. Since the end of the start-up and optimization phase, emission rate has stayed below the 104.5 lb/hr limit of equivalent SO{sub 2} (based on a 24-hr average). In Jan. 1995, the emission rate from the sulfur removal facility averaged 86.7 lb/hr with less than 20 lb/hr from the Econobator exhaust. The challenges yet to be met are decreasing the operating expenses of the sulfur removal facility, notably chemical costs, and minimizing the impact of the heating system on unit reliability.

Havili, M.U.; Fraser-Smyth, L.L.; Wood, B.W. [Geneva Steel, Provo, UT (United States)

1996-02-01T23:59:59.000Z

202

Energy Basics: Ultra-Low Sulfur Diesel Fuel  

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

EERE: Energy Basics Ultra-Low Sulfur Diesel Fuel Ultra-low sulfur diesel (ULSD) is diesel fuel with 15 parts per million or lower sulfur content. The U.S. Environmental Protection...

203

Lithium Polysulfidophosphates: A Family of Lithium-Conducting Sulfur-Rich Compounds for Lithium-Sulfur Batteries  

SciTech Connect

Given the great potential for improving the energy density of state-of-the-art lithium-ion batteries by a factor of 5, a breakthrough in lithium-sulfur (Li-S) batteries will have a dramatic impact in a broad scope of energy related fields. Conventional Li-S batteries that use liquid electrolytes are intrinsically short-lived with low energy efficiency. The challenges stem from the poor electronic and ionic conductivities of elemental sulfur and its discharge products. We report herein lithium polysulfidophosphates (LPSP), a family of sulfur-rich compounds, as the enabler of long-lasting and energy-efficient Li-S batteries. LPSP have ionic conductivities of 3.0 10-5 S cm-1 at 25 oC, which is 8 orders of magnitude higher than that of Li2S (~10-13 S cm-1). The high Li-ion conductivity of LPSP is the salient characteristic of these compounds that impart the excellent cycling performance to Li-S batteries. In addition, the batteries are configured in an all-solid state that promises the safe cycling of high-energy batteries with metallic lithium anodes.

Lin, Zhan [ORNL; Liu, Zengcai [ORNL; Fu, Wujun [ORNL; Dudney, Nancy J [ORNL; Liang, Chengdu [ORNL

2013-01-01T23:59:59.000Z

204

Sulfur oxide adsorbents and emissions control  

DOE Patents (OSTI)

High capacity sulfur oxide absorbents utilizing manganese-based octahedral molecular sieve (Mn--OMS) materials are disclosed. An emissions reduction system for a combustion exhaust includes a scrubber 24 containing these high capacity sulfur oxide absorbents located upstream from a NOX filter 26 or particulate trap.

Li, Liyu (Richland, WA); King, David L. (Richland, WA)

2006-12-26T23:59:59.000Z

205

Economic comparison of hydrogen production using sulfuric acid electrolysis and sulfur cycle water decomposition. Final report  

SciTech Connect

An evaluation of the relative economics of hydrogen production using two advanced techniques was performed. The hydrogen production systems considered were the Westinghouse Sulfur Cycle Water Decomposition System and a water electrolysis system employing a sulfuric acid electrolyte. The former is a hybrid system in which hydrogen is produced in an electrolyzer which uses sulfur dioxide to depolarize the anode. The electrolyte is sulfuric acid. Development and demonstration efforts have shown that extremely low cell voltages can be achieved. The second system uses a similar sulfuric acid electrolyte technology in water electrolysis cells. The comparative technoeconomics of hydrogen produced by the hybrid Sulfur Cycle and by water electrolysis using a sulfuric acid electrolyte were determined by assessing the performance and economics of 380 million SCFD plants, each energized by a very high temperature nuclear reactor (VHTR). The evaluation concluded that the overall efficiencies of hydrogen production, for operating parameters that appear reasonable for both systems, are approximately 41% for the sulfuric acid electrolysis and 47% for the hybrid Sulfur Cycle. The economic evaluation of hydrogen production, based on a 1976 cost basis and assuming a developed technology for both hydrogen production systems and the VHTRs, indicated that the hybrid Sulfur Cycle could generate hydrogen for a total cost approximately 6 to 7% less than the cost from the sulfuric acid electrolysis plant.

Farbman, G.H.; Krasicki, B.R.; Hardman, C.C.; Lin, S.S.; Parker, G.H.

1978-06-01T23:59:59.000Z

206

CGC Trace Species Partitioning  

NLE Websites -- All DOE Office Websites (Extended Search)

Trace Species Partitioning as Affected Trace Species Partitioning as Affected by Cold Gas Cleanup Conditions: A Thermodynamic Analysis February 10, 2011 DOE/NETL-2011/1503 T r ace Species P ar titioning at C old G as C leanup C onditions Disclaimer This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor 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 therein to any specific commercial product, process, or service by trade name,

207

Sulfur-Iodine thermochemical cycle for hydrogen production.  

E-Print Network (OSTI)

??The aim of the thesis was to study the Sulfur-Iodine thermochemical cycle for hydrogen production. There were three reactions in this cycle: Bunsen reaction, sulfuric (more)

Dan, Huang

2009-01-01T23:59:59.000Z

208

Method of removal of sulfur from coal and petroleum products  

DOE Patents (OSTI)

A method for the removal of sulfur from sulfur-bearing materials such as coal and petroleum products using organophosphine and organophosphite compounds is provided.

Verkade, John G. (Ames, IA); Mohan, Thyagarajan (Ames, IA); Angelici, Robert J. (Ames, IA)

1995-01-01T23:59:59.000Z

209

Production of low-sulfur binder pitch from high-sulfur Illinois coals. Technical report, September 1--November 30, 1994  

Science Conference Proceedings (OSTI)

The objective of this project is to produce electrode binder pitch with sulfur content below 0.6 wt% from high-sulfur Illinois coal mild gasification liquids. In this project, two approaches to sulfur reduction are being explored in conjunction with thermocracking: (1) the use of conventionally cleaned coal with low ({approximately}1%) sulfur as a mild gasification feedstock, and (2) direct biodesulfurization of the liquids prior to thermocracking. In Case 1, the crude pitch is being produced by mild gasification of IBC-109 coal in an existing IGT bench-scale reactor, followed by distillation of the scrubbing solvent and light-to-middle oils to isolate the crude pitch. In Case 2, the crude pitch for biodesulfurization is the same material previously studied, which was obtained from Illinois No. 6 coal tests conducted in the IGT mild gasification PRU in 1990. Biodesulfurization is to be performed by contacting the pitch with Rhodococcus Rhodochrous either as live cultures or in the form of concentrated biocatalyst. Following preparation of the crude pitches, pitch upgrading experiments are to be conducted in a continuous flash thermocracker (FTC) constructed in previous ICCI-sponsored studies. The finished pitch is then characterized for physical and chemical properties (density, softening point, QI, TI, coking value, and elemental composition), and compared to typical specifications for binder pitches. This quarter, 45 kg of IBC-109 coal was obtained and sized to 40 x 80 mesh for mild gasification. Laboratory experiments were conducted to identify means of dispersing or emulsifying pitch in water to render is accessible to biocatalysts, and exploratory desulfurization tests on one-gram pitch samples were begun.

Knight, R.A. [Inst. of Gas Technology, Chicago, IL (United States)

1994-12-31T23:59:59.000Z

210

It's Elemental - The Element Lithium  

NLE Websites -- All DOE Office Websites (Extended Search)

(Helium) The Periodic Table of Elements Next Element (Beryllium) Beryllium The Element Lithium Click for Isotope Data 3 Li Lithium 6.941 Atomic Number: 3 Atomic Weight: 6.941...

211

In-place wellbore consolidation in petroleum reservoirs using sulfur-oil polymers  

SciTech Connect

This patent describes a method for reducing the production from an unconsolidated subterranean hydrocarbon formation penetrated by a wellbore while leaving the formation permeable to the flow of formation fluids. The method consists of injecting steam carrying droplets of elemental liquid sulfur into the formation. The next step consists of allowing the injected sulfur to react with the hydrocarbon in the formation to produce a consolidating agent which extends outward radially from the wellbore. The last step in the process follows from the radial extension of the consolidating agent in its causing the reduction in production of hydrocarbons from the formation.

Rubinstein, I.; Woodford, R.B.

1986-01-14T23:59:59.000Z

212

It's Elemental - The Element Plutonium  

NLE Websites -- All DOE Office Websites (Extended Search)

Next Element (Americium) Americium The Element Plutonium Click for Isotope Data 94 Pu Plutonium 244 Atomic Number: 94 Atomic Weight: 244 Melting Point: 913 K (640C or...

213

Trace metals in sediments of coastal Siberia  

E-Print Network (OSTI)

For the work described in this thesis, a total of 218 samples from 104 cores from the East Siberian, Laptev, Kara, and Pechora Seas and the Ob and Yenisei Rivers were analyzed for the trace metals Ag, As, Ba, Cd, Cr, Cu, Fe, Hg, Ni, Pb, Sb, and Zn. To make comparisons between locations easier, the concentration of all elements was normalized to Fe to account for variability in grain size and mineralogy. For the metals Ag, Cd, and Hg there was poor correlation with Fe, likely partially due to analytical variations caused by the low concentrations of these elements. Copper, Ni and Zn showed good correlation with Fe, suggesting these elements are from natural inputs to the sediments. Arsenic, Ba, Cr, Pb, and Sb showed variable correlations, suggesting a more mafic (basaltic) mineral phase at some locations and/or diagenetic redistribution of these metals. No statistically significant differences were found between metal to Fe ratios at the surface (0-2.5 cm) of the sediment cores and the bottoms (5- 1 00 cm), with a few exceptions. There was also no statistically significant difference in the average metal to Fe ratios of the East Siberian and Laptev Seas. There was, however, a significant difference when these two seas were compared to the Kara and Pechora Seas, suggesting different mineralogy in the drainage basins of eastern and western Siberia. Sediment from the Kara Sea was similar in trace metal concentration to sediment from its likely source, the Ob and Yenisei rivers.

Esnough, Teresa Elizabeth

1996-01-01T23:59:59.000Z

214

Flexible reference trace reduction for VM simulations  

Science Conference Proceedings (OSTI)

The unmanageably large size of reference traces has spurred the development of sophisticated trace reduction techniques. In this article we present two new algorithms for trace reduction: Safely Allowed Drop (SAD) and Optimal LRU Reduction ... Keywords: cache hierarchies, locality, reference traces, trace compression, trace reduction

Scott F. Kaplan; Yannis Smaragdakis; Paul R. Wilson

2003-01-01T23:59:59.000Z

215

Sulfur-graphene oxide material for lithium-sulfur battery cathodes  

NLE Websites -- All DOE Office Websites (Extended Search)

Sulfur-graphene oxide material for lithium-sulfur battery cathodes Sulfur-graphene oxide material for lithium-sulfur battery cathodes Theoretical specific energy and theoretical energy density Scanning electron micrograph of the GO-S nanocomposite June 2013 Searching for a safer, less expensive alternative to today's lithium-ion batteries, scientists have turned to lithium-sulfur as a possible chemistry for next-generation batteries. Li/S batteries have several times the energy storage capacity of the best currently available rechargeable Li-ion battery, and sulfur is inexpensive and nontoxic. Current batteries using this chemistry, however, suffer from extremely short cycle life-they don't last through many charge-discharge cycles before they fail. A research team led by Elton Cairns and Yuegang Zhang has developed a new

216

Appalachian No. 1 Refinery District Sulfur Content (Weighted ...  

U.S. Energy Information Administration (EIA)

Appalachian No. 1 Refinery District Sulfur Content (Weighted Average) of Crude Oil Input to Refineries (Percent)

217

Sulfur Resistant Electrodes for Zirconia Oxygen Sensors ...  

Prototype - A zirconia O2 sensor with a Tb-YSZ electrode was tested in a high sulfur coal fired power plant side by side with a normal zirconia O2 ...

218

Process for removing sulfur from coal  

DOE Patents (OSTI)

A process is disclosed for the removal of divalent organic and inorganic sulfur compounds from coal and other carbonaceous material. A slurry of pulverized carbonaceous material is contacted with an electrophilic oxidant which selectively oxidizes the divalent organic and inorganic compounds to trivalent and tetravalent compounds. The carbonaceous material is then contacted with a molten caustic which dissolves the oxidized sulfur compounds away from the hydrocarbon matrix.

Aida, T.; Squires, T.G.; Venier, C.G.

1983-08-11T23:59:59.000Z

219

Copper mercaptides as sulfur dioxide indicators  

DOE Patents (OSTI)

Organophosphine copper(I) mercaptide complexes are useful as convenient and semiquantitative visual sulfur dioxide gas indicators. The air-stable complexes form 1:1 adducts in the presence of low concentrations of sulfur dioxide gas, with an associated color change from nearly colorless to yellow-orange. The mercaptides are made by mixing stoichiometric amounts of the appropriate copper(I) mercaptide and phosphine in an inert organic solvent.

Eller, Phillip G. (Los Alamos, NM); Kubas, Gregory J. (Los Alamos, NM)

1979-01-01T23:59:59.000Z

220

Trace Element Analysis At Roosevelt Hot Springs Area (Christensen...  

Open Energy Info (EERE)

fluid conduits; and (5) deposits of calcium carbonate where flashing of brine to steam due to pressure release has occurred. References Odin D. Christensen, Regina A....

Note: This page contains sample records for the topic "trace elements 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

Trace-Element Distribution In An Active Hydrothermal System,...  

Open Energy Info (EERE)

flow-controlling fractures; (5) deposits of CaCO3 at depth where flashing of brine to steam has occurred due to pressure release. The geochemical enrichments are not, in...

222

The Deportment of Trace Toxic Elements in Cyanide Solutions  

Science Conference Proceedings (OSTI)

Stratigraphy, Mineralogy, Geochemistry, and Genesis of the Au-Rich Volcanogenic Massive Sulfide (VMS) System from the Baie Verte Peninsula, NW

223

Tracing element sources of hydrothermal mineral deposits: REE and ...  

Science Conference Proceedings (OSTI)

inclusion studies are the only way to obtain direct evidence from these ... and eastern part of the Derbyshire Dome (Fig. 1). The ... calcite is more abundant in the western part of the vein ...... and hydrothermal fluids, it is hard to understand why.

224

It's Elemental - Element Concentration Game  

NLE Websites -- All DOE Office Websites (Extended Search)

symbols of the elements. After you have had time to study the cards, the computer will flip them over and ask you to find a particular element. Click on the card that contains...

225

Trace Anomaly in Geometric Discretization  

E-Print Network (OSTI)

I develop the simplest geometric-discretized analogue of two dimensional scalar field theory, which qualitatively reproduces the trace anomaly of the continuous theory. The discrete analogue provides an interpretation of the trace anomaly in terms of a non-trivial transformation of electric-magnetic duality-invariant modes of resistor networks that accommodate both electric and magnetic charge currents.

Czech, B

2007-01-01T23:59:59.000Z

226

Optimally profiling and tracing programs  

Science Conference Proceedings (OSTI)

This paper describes algorithms for inserting monitoring code to profile and trace programs. These algorithms greatly reduce the cost of measuring programs with respect to the commonly used technique of placing code in each basic block. Program profiling ... Keywords: control-flow graph, instruction tracing, instrumentation, profiling

Thomas Ball; James R. Larus

1994-07-01T23:59:59.000Z

227

Parallel, high-resolution carbon and sulfur isotope records of the evolving Paleozoic marine sulfur reservoir  

E-Print Network (OSTI)

. Carbonate rocks record the inorganic carbon isotope composition of the oceanic reservoir through geologicalParallel, high-resolution carbon and sulfur isotope records of the evolving Paleozoic marine sulfur, University of California-Riverside, Riverside California 92521-0423, USA b Department of Geological Sciences

Saltzman, Matthew R.

228

Zevenhoven & Kilpinen TRACE ELEMENTS, ALKALI METALS 19.6.2001 8-1 Chapter 8 Trace elements,  

E-Print Network (OSTI)

­3109. (28) Niksa, S.; Fujiwara, N. Predicting extents of mercury oxidation in coal-derived flue gases. J, 1365­1371. (6) Presto, A. A.; Granite, E. J. Survey of catalysts for oxidation of mercury in flue gas mercury (Hg0) from simulated coal-combustion flue gas. Experiments were carried out in fixed-bed reactors

Laughlin, Robert B.

229

HELSINKI UNIVERSITY OF TECHNOLOGY ENE-47.153 Trace elements and alkaliTrace elements and alkali  

E-Print Network (OSTI)

REGULATIONS Although incinerator flue gas emission limits for acid gases have been imposed by the federal, such as sodium chlorite (NaCI02), is added to oxidize flue gas NO to N02, which can be removed by a sodium of saturated flue gas to approximately 60°C ( 140°F), the total (par ticulate and gaseous) mercury emissions

Zevenhoven, Ron

230

THE EFFECT OF ANOLYTE PRODUCT ACID CONCENTRATION ON HYBRID SULFUR CYCLE PERFORMANCE  

DOE Green Energy (OSTI)

The Hybrid Sulfur (HyS) cycle (Fig. 1) is one of the simplest, all-fluids thermochemical cycles that has been devised for splitting water with a high-temperature nuclear or solar heat source. It was originally patented by Brecher and Wu in 1975 and extensively developed by Westinghouse in the late 1970s and early 1980s. As its name suggests, the only element used besides hydrogen and oxygen is sulfur, which is cycled between the +4 and +6 oxidation states. HyS comprises two steps. One is the thermochemical (>800 C) decomposition of sulfuric acid (H{sub 2}SO{sub 4}) to sulfur dioxide (SO{sub 2}), oxygen (O{sub 2}), and water. H{sub 2}SO{sub 4} = SO{sub 2} + 1/2 O{sub 2} + H{sub 2}O. The other is the SO{sub 2}-depolarized electrolysis of water to H{sub 2}SO{sub 4} and hydrogen (H{sub 2}), SO{sub 2} + 2 H{sub 2}O = H{sub 2}SO{sub 4} + H{sub 2}, E{sup o} = -0.156 V, explaining the 'hybrid' designation. These two steps taken together split water into H{sub 2} and O{sub 2} using heat and electricity. Researchers at the Savannah River National Laboratory (SRNL) and at the University of South Carolina (USC) have successfully demonstrated the use of proton exchange membrane (PEM) electrolyzers (Fig. 2) for the SO{sub 2}-depolarized electrolysis (sulfur oxidation) step, while Sandia National Laboratories (SNL) successfully demonstrated the high-temperature sulfuric acid decomposition (sulfur reduction) step using a bayonet-type reactor (Fig. 3). This latter work was performed as part of the Sulfur-Iodine (SI) cycle Integrated Laboratory Scale demonstration at General Atomics (GA). The combination of these two operations results in a simple process that will be more efficient and cost-effective for the massive production of hydrogen than alkaline electrolysis. Recent developments suggest that the use of PEMs other than Nafion will allow sulfuric acid to be produced at higher concentrations (>60 wt%), offering the possibility of net thermal efficiencies around 50% (HHV basis). The effect of operation at higher anolyte concentrations on the flowsheet, and on the net thermal efficiency for a nuclear-heated HyS process, is examined and quantified.

Gorensek, M.; Summers, W.

2010-03-24T23:59:59.000Z

231

It's Elemental - The Element Europium  

NLE Websites -- All DOE Office Websites (Extended Search)

Samarium Samarium Previous Element (Samarium) The Periodic Table of Elements Next Element (Gadolinium) Gadolinium The Element Europium [Click for Isotope Data] 63 Eu Europium 151.964 Atomic Number: 63 Atomic Weight: 151.964 Melting Point: 1095 K (822°C or 1512°F) Boiling Point: 1802 K (1529°C or 2784°F) Density: 5.24 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: none Group Name: Lanthanide What's in a name? Named after the continent of Europe. Say what? Europium is pronounced as yoo-RO-pee-em. History and Uses: Europium was discovered by Eugène-Antole Demarçay, a French chemist, in 1896. Demarçay suspected that samples of a recently discovered element, samarium, were contaminated with an unknown element. He was able to produce

232

It's Elemental - The Element Potassium  

NLE Websites -- All DOE Office Websites (Extended Search)

Argon Argon Previous Element (Argon) The Periodic Table of Elements Next Element (Calcium) Calcium The Element Potassium [Click for Isotope Data] 19 K Potassium 39.0983 Atomic Number: 19 Atomic Weight: 39.0983 Melting Point: 336.53 K (63.38°C or 146.08°F) Boiling Point: 1032 K (759°C or 1398°F) Density: 0.89 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 4 Group Number: 1 Group Name: Alkali Metal What's in a name? From the English word potash. Potassium's chemical symbol comes from the Latin word for alkali, kalium. Say what? Potassium is pronounced as poh-TASS-ee-em. History and Uses: Although potassium is the eighth most abundant element on earth and comprises about 2.1% of the earth's crust, it is a very reactive element

233

It's Elemental - The Element Magnesium  

NLE Websites -- All DOE Office Websites (Extended Search)

Sodium Sodium Previous Element (Sodium) The Periodic Table of Elements Next Element (Aluminum) Aluminum The Element Magnesium [Click for Isotope Data] 12 Mg Magnesium 24.3050 Atomic Number: 12 Atomic Weight: 24.3050 Melting Point: 923 K (650°C or 1202°F) Boiling Point: 1363 K (1090°C or 1994°F) Density: 1.74 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 3 Group Number: 2 Group Name: Alkaline Earth Metal What's in a name? For Magnesia, a district in the region of Thessaly, Greece. Say what? Magnesium is pronounced as mag-NEE-zhi-em. History and Uses: Although it is the eighth most abundant element in the universe and the seventh most abundant element in the earth's crust, magnesium is never found free in nature. Magnesium was first isolated by Sir Humphry Davy, an

234

Tracing Geothermal Fluids  

DOE Green Energy (OSTI)

Geothermal water must be injected back into the reservoir after it has been used for power production. Injection is critical in maximizing the power production and lifetime of the reservoir. To use injectate effectively the direction and velocity of the injected water must be known or inferred. This information can be obtained by using chemical tracers to track the subsurface flow paths of the injected fluid. Tracers are chemical compounds that are added to the water as it is injected back into the reservoir. The hot production water is monitored for the presence of this tracer using the most sensitive analytic methods that are economically feasible. The amount and concentration pattern of the tracer revealed by this monitoring can be used to evaluate how effective the injection strategy is. However, the tracers must have properties that suite the environment that they will be used in. This requires careful consideration and testing of the tracer properties. In previous and parallel investigations we have developed tracers that are suitable from tracing liquid water. In this investigation, we developed tracers that can be used for steam and mixed water/steam environments. This work will improve the efficiency of injection management in geothermal fields, lowering the cost of energy production and increasing the power output of these systems.

Michael C. Adams; Greg Nash

2004-03-01T23:59:59.000Z

235

Low quality natural gas sulfur removal/recovery  

Science Conference Proceedings (OSTI)

The project comprises a Base Program and an Optional Program. The Base Program, which included NEPA reporting, process design and an experimental research plan for the optional program, was completed August 31, 1993 with submission of the Task 2 Final Report. The Optional Program, Task 3, began in July 1994. The project goal is to further develop and demonstrate two of the component technologies of the CFZ-CNG Process: (1) pilot-scale triple-point crystallization of carbon dioxide, producing commercially pure carbon dioxide from contaminated carbon dioxide at the rate of 25 ton/day, and (2) bench-scale modified high pressure Claus technology, recovering elemental sulfur from hydrogen sulfide at the rate of 200 lb/day.

Siwajek, L.A. [Acrion Technologies, Inc., Cleveland, OH (United States); Kuehn, L. [Bovar Corp., Houston, TX (United States). Western Research

1995-06-01T23:59:59.000Z

236

ALTERNATIVE FLOWSHEETS FOR THE SULFUR-IODINE THERMOCHEMICAL HYDROGEN CYCLE  

DOE Green Energy (OSTI)

OAK-B135 A hydrogen economy will need significant new sources of hydrogen. Unless large-scale carbon sequestration can be economically implemented, use of hydrogen reduces greenhouse gases only if the hydrogen is produced with non-fossil energy sources. Nuclear energy is one of the limited options available. One of the promising approaches to produce large quantities of hydrogen from nuclear energy efficiently is the Sulfur-Iodine (S-I) thermochemical water-splitting cycle, driven by high temperature heat from a helium Gas-Cooled Reactor. They have completed a study of nuclear-driven thermochemical water-splitting processes. The final task of this study was the development of a flowsheet for a prototype S-I production plant. An important element of this effort was the evaluation of alternative flowsheets and selection of the reference design.

BROWN,LC; LENTSCH,RD; BESENBRUCH,GE; SCHULTZ,KR; FUNK,JE

2003-02-01T23:59:59.000Z

237

It's Elemental - The Element Nitrogen  

NLE Websites -- All DOE Office Websites (Extended Search)

Carbon Carbon Previous Element (Carbon) The Periodic Table of Elements Next Element (Oxygen) Oxygen The Element Nitrogen [Click for Isotope Data] 7 N Nitrogen 14.0067 Atomic Number: 7 Atomic Weight: 14.0067 Melting Point: 63.15 K (-210.00°C or -346.00°F) Boiling Point: 77.36 K (-195.79°C or -320.44°F) Density: 0.0012506 grams per cubic centimeter Phase at Room Temperature: Gas Element Classification: Non-metal Period Number: 2 Group Number: 15 Group Name: Pnictogen What's in a name? From the Greek words nitron and genes, which together mean "saltpetre forming." Say what? Nitrogen is pronounced as NYE-treh-gen. History and Uses: Nitrogen was discovered by the Scottish physician Daniel Rutherford in 1772. It is the fifth most abundant element in the universe and makes up

238

It's Elemental - The Element Sodium  

NLE Websites -- All DOE Office Websites (Extended Search)

Neon Neon Previous Element (Neon) The Periodic Table of Elements Next Element (Magnesium) Magnesium The Element Sodium [Click for Isotope Data] 11 Na Sodium 22.98976928 Atomic Number: 11 Atomic Weight: 22.98976928 Melting Point: 370.95 K (97.80°C or 208.04°F) Boiling Point: 1156 K (883°C or 1621°F) Density: 0.97 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 3 Group Number: 1 Group Name: Alkali Metal What's in a name? From the English word soda and from the Medieval Latin word sodanum, which means "headache remedy." Sodium's chemical symbol comes from the Latin word for sodium carbonate, natrium. Say what? Sodium is pronounced as SO-dee-em. History and Uses: Although sodium is the sixth most abundant element on earth and comprises

239

It's Elemental - The Element Francium  

NLE Websites -- All DOE Office Websites (Extended Search)

Radon Radon Previous Element (Radon) The Periodic Table of Elements Next Element (Radium) Radium The Element Francium [Click for Isotope Data] 87 Fr Francium 223 Atomic Number: 87 Atomic Weight: 223 Melting Point: 300 K (27°C or 81°F) Boiling Point: Unknown Density: Unknown Phase at Room Temperature: Solid Element Classification: Metal Period Number: 7 Group Number: 1 Group Name: Alkali Metal Radioactive What's in a name? Named for the country of France. Say what? Francium is pronounced as FRAN-see-em. History and Uses: Francium was discovered by Marguerite Catherine Perey, a French chemist, in 1939 while analyzing actinium's decay sequence. Although considered a natural element, scientists estimate that there is no more than one ounce of francium in the earth's crust at one time. Since there is so little

240

It's Elemental - The Element Neon  

NLE Websites -- All DOE Office Websites (Extended Search)

Fluorine Fluorine Previous Element (Fluorine) The Periodic Table of Elements Next Element (Sodium) Sodium The Element Neon [Click for Isotope Data] 10 Ne Neon 20.1797 Atomic Number: 10 Atomic Weight: 20.1797 Melting Point: 24.56 K (-248.59°C or -415.46°F) Boiling Point: 27.07 K (-246.08°C or -410.94°F) Density: 0.0008999 grams per cubic centimeter Phase at Room Temperature: Gas Element Classification: Non-metal Period Number: 2 Group Number: 18 Group Name: Noble Gas What's in a name? From the Greek word for new, neos. Say what? Neon is pronounced as NEE-on. History and Uses: Neon was discovered by Sir William Ramsay, a Scottish chemist, and Morris M. Travers, an English chemist, shortly after their discovery of the element krypton in 1898. Like krypton, neon was discovered through the

Note: This page contains sample records for the topic "trace elements 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

It's Elemental - The Element Technetium  

NLE Websites -- All DOE Office Websites (Extended Search)

Molybdenum Molybdenum Previous Element (Molybdenum) The Periodic Table of Elements Next Element (Ruthenium) Ruthenium The Element Technetium [Click for Isotope Data] 43 Tc Technetium 98 Atomic Number: 43 Atomic Weight: 98 Melting Point: 2430 K (2157°C or 3915°F) Boiling Point: 4538 K (4265°C or 7709°F) Density: 11 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 5 Group Number: 7 Group Name: none Radioactive and Artificially Produced What's in a name? From the Greek word for artificial, technetos. Say what? Technetium is pronounced as tek-NEE-she-em. History and Uses: Technetium was the first artificially produced element. It was isolated by Carlo Perrier and Emilio Segrè in 1937. Technetium was created by bombarding molybdenum atoms with deuterons that had been accelerated by a

242

It's Elemental - The Element Cobalt  

NLE Websites -- All DOE Office Websites (Extended Search)

Iron Iron Previous Element (Iron) The Periodic Table of Elements Next Element (Nickel) Nickel The Element Cobalt [Click for Isotope Data] 27 Co Cobalt 58.933195 Atomic Number: 27 Atomic Weight: 58.933195 Melting Point: 1768 K (1495°C or 2723°F) Boiling Point: 3200 K (2927°C or 5301°F) Density: 8.86 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 4 Group Number: 9 Group Name: none What's in a name? From the German word for goblin or evil spirit, kobald and the Greek word for mine, cobalos. Say what? Cobalt is pronounced as KO-bolt. History and Uses: Cobalt was discovered by Georg Brandt, a Swedish chemist, in 1739. Brandt was attempting to prove that the ability of certain minerals to color glass blue was due to an unknown element and not to bismuth, as was commonly

243

It's Elemental - The Element Bromine  

NLE Websites -- All DOE Office Websites (Extended Search)

Selenium Selenium Previous Element (Selenium) The Periodic Table of Elements Next Element (Krypton) Krypton The Element Bromine [Click for Isotope Data] 35 Br Bromine 79.904 Atomic Number: 35 Atomic Weight: 79.904 Melting Point: 265.95 K (-7.2°C or 19.0°F) Boiling Point: 331.95 K (58.8°C or 137.8°F) Density: 3.11 grams per cubic centimeter Phase at Room Temperature: Liquid Element Classification: Non-metal Period Number: 4 Group Number: 17 Group Name: Halogen What's in a name? From the Greek word for stench, bromos. Say what? Bromine is pronounced as BRO-meen. History and Uses: The only nonmetallic element that is a liquid at normal room temperatures, bromine was produced by Carl Löwig, a young chemistry student, the summer before starting his freshman year at Heidelberg. When he showed his

244

It's Elemental - The Element Oxygen  

NLE Websites -- All DOE Office Websites (Extended Search)

Nitrogen Nitrogen Previous Element (Nitrogen) The Periodic Table of Elements Next Element (Fluorine) Fluorine The Element Oxygen [Click for Isotope Data] 8 O Oxygen 15.9994 Atomic Number: 8 Atomic Weight: 15.9994 Melting Point: 54.36 K (-218.79°C or -361.82°F) Boiling Point: 90.20 K (-182.95°C or -297.31°F) Density: 0.001429 grams per cubic centimeter Phase at Room Temperature: Gas Element Classification: Non-metal Period Number: 2 Group Number: 16 Group Name: Chalcogen What's in a name? From the greek words oxys and genes, which together mean "acid forming." Say what? Oxygen is pronounced as OK-si-jen. History and Uses: Oxygen had been produced by several chemists prior to its discovery in 1774, but they failed to recognize it as a distinct element. Joseph

245

It's Elemental - The Element Manganese  

NLE Websites -- All DOE Office Websites (Extended Search)

Chromium Chromium Previous Element (Chromium) The Periodic Table of Elements Next Element (Iron) Iron The Element Manganese [Click for Isotope Data] 25 Mn Manganese 54.938045 Atomic Number: 25 Atomic Weight: 54.938045 Melting Point: 1519 K (1246°C or 2275°F) Boiling Point: 2334 K (2061°C or 3742°F) Density: 7.3 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 4 Group Number: 7 Group Name: none What's in a name? From the Latin word for magnet, magnes. Say what? Manganese is pronounced as MAN-ge-nees. History and Uses: Proposed to be an element by Carl Wilhelm Scheele in 1774, manganese was discovered by Johan Gottlieb Gahn, a Swedish chemist, by heating the mineral pyrolusite (MnO2) in the presence of charcoal later that year.

246

It's Elemental - The Element Titanium  

NLE Websites -- All DOE Office Websites (Extended Search)

Scandium Scandium Previous Element (Scandium) The Periodic Table of Elements Next Element (Vanadium) Vanadium The Element Titanium [Click for Isotope Data] 22 Ti Titanium 47.867 Atomic Number: 22 Atomic Weight: 47.867 Melting Point: 1941 K (1668°C or 3034°F) Boiling Point: 3560 K (3287°C or 5949°F) Density: 4.5 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 4 Group Number: 4 Group Name: none What's in a name? From the Greek word Titans, the mythological "first sons of the Earth." Say what? Titanium is pronounced as tie-TAY-nee-em. History and Uses: Titanium was discovered in 1791 by the Reverend William Gregor, an English pastor. Pure titanium was first produced by Matthew A. Hunter, an American metallurgist, in 1910. Titanium is the ninth most abundant element in the

247

It's Elemental - The Element Cerium  

NLE Websites -- All DOE Office Websites (Extended Search)

Lanthanum Lanthanum Previous Element (Lanthanum) The Periodic Table of Elements Next Element (Praseodymium) Praseodymium The Element Cerium [Click for Isotope Data] 58 Ce Cerium 140.116 Atomic Number: 58 Atomic Weight: 140.116 Melting Point: 1071 K (798°C or 1468°F) Boiling Point: 3697 K (3424°C or 6195°F) Density: 6.770 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: none Group Name: Lanthanide What's in a name? Named for the asteroid Ceres. Say what? Cerium is pronounced as SER-ee-em. History and Uses: Cerium was discovered by Jöns Jacob Berzelius and Wilhelm von Hisinger, Swedish chemists, and independently by Martin Heinrich Klaproth, a German chemist, in 1803. Cerium is the most abundant of the rare earth elements

248

It's Elemental - Isotopes of the Element Neptunium  

NLE Websites -- All DOE Office Websites (Extended Search)

Uranium Previous Element (Uranium) The Periodic Table of Elements Next Element (Plutonium) Plutonium Isotopes of the Element Neptunium Click for Main Data Most of the isotope...

249

It's Elemental - Isotopes of the Element Nobelium  

NLE Websites -- All DOE Office Websites (Extended Search)

Mendelevium Previous Element (Mendelevium) The Periodic Table of Elements Next Element (Lawrencium) Lawrencium Isotopes of the Element Nobelium Click for Main Data Most of the...

250

It's Elemental - Isotopes of the Element Fermium  

NLE Websites -- All DOE Office Websites (Extended Search)

Einsteinium Previous Element (Einsteinium) The Periodic Table of Elements Next Element (Mendelevium) Mendelevium Isotopes of the Element Fermium Click for Main Data Most of the...

251

It's Elemental - Isotopes of the Element Argon  

NLE Websites -- All DOE Office Websites (Extended Search)

Chlorine Previous Element (Chlorine) The Periodic Table of Elements Next Element (Potassium) Potassium Isotopes of the Element Argon Click for Main Data Most of the isotope data...

252

It's Elemental - Isotopes of the Element Ruthenium  

NLE Websites -- All DOE Office Websites (Extended Search)

Technetium Previous Element (Technetium) The Periodic Table of Elements Next Element (Rhodium) Rhodium Isotopes of the Element Ruthenium Click for Main Data Most of the isotope...

253

It's Elemental - Isotopes of the Element Molybdenum  

NLE Websites -- All DOE Office Websites (Extended Search)

Niobium Previous Element (Niobium) The Periodic Table of Elements Next Element (Technetium) Technetium Isotopes of the Element Molybdenum Click for Main Data Most of the isotope...

254

It's Elemental - Isotopes of the Element Protactinium  

NLE Websites -- All DOE Office Websites (Extended Search)

Thorium Previous Element (Thorium) The Periodic Table of Elements Next Element (Uranium) Uranium Isotopes of the Element Protactinium Click for Main Data Most of the isotope data...

255

Sulfur isotopic evidence for controls on sulfur incorporation in peat and coal  

Science Conference Proceedings (OSTI)

Pyritic sulfur isotope [delta][sup 34]S values were used as a measure of two principal controls on sulfur incorporation in peat and coal: the availability of sulfate, and the activity of sulfate-reducing bacteria in the peat-forming mire. Relatively low [delta][sup 34]S values indicated an open system with a relatively abundant supply of sulfate that exceeded the rate of sulfate reduction to sulfide, whereas relatively high [delta][sup 34]S values indicated a closed system with a more limited supply of sulfate. For example, in the high-sulfur (>3% S), Holocene deposits of Mud Lake, Florida, pyritic sulfur [delta][sup 34]S values decreasing sharply across the transition from peat to the overlying lacustrine sapropel, which corresponds to an increased supply of sulfate from the lake waters. Likewise, syngenetic pyrite in the high-sulfur Minto coal bed (Pictou Group, Westphalian C) in New Brunswick, Canada, show up to 10% negative shifts in [delta][sup 34]S in attrital layers containing detrital quartz and illite, consistent with an increased supply of sulfate from streams entering the peat-forming mire. In contrast, positive pyritic sulfur [delta][sup 34]S values in high-sulfur, channel-fill coal beds (lower Breathitt Formation, Middle Pennsylvanian) in eastern Kentucky indicate that a steady supply of sulfate was exhausted by very active microbial sulfate reduction in the channel-fill peat.

Spiker, E.C.; Bates, A.L. (Geological Survey, Reston, VA (United States))

1993-08-01T23:59:59.000Z

256

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

Science Conference Proceedings (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

257

Treatability study on the use of by-product sulfur in Kazakhstan for the stabilization of hazardous and radioactive wastes  

Science Conference Proceedings (OSTI)

The Republic of Kazakhstan generates significant quantities of excess elemental sulfur from the production and refining of petroleum reserves. In addition, the country also produces hazardous, and radioactive wastes which require treatment/stabilization. In an effort to find secondary uses for the elemental sulfur, and simultaneously produce a material which could be used to encapsulate, and reduce the dispersion of harmful contaminants into the environment, BNL evaluated the use of the sulfur polymer cement (SPC) produced from by-product sulfur in Kazakhstan. This thermoplastic binder material forms a durable waste form with low leaching properties and is compatible with a wide range of waste types. Several hundred kilograms of Kazakhstan sulfur were shipped to the US and converted to SPC (by reaction with 5 wt% organic modifiers) for use in this study. A phosphogypsum sand waste generated in Kazakhstan during the purification of phosphate fertilizer was selected for treatment. Waste loadings of 40 wt% were easily achieved. Waste form performance testing included compressive strength, water immersion, and Accelerated Leach Testing.

Kalb, P.D.; Milian, L.W. [Brookhaven National Lab., Upton, NY (United States). Environmental and Waste Technology Center; Yim, S.P. [Korea Atomic Energy Research Inst. (Korea, Republic of); Dyer, R.S.; Michaud, W.R. [Environmental Protection Agency (United States)

1997-12-01T23:59:59.000Z

258

It's Elemental - The Element Tungsten  

NLE Websites -- All DOE Office Websites (Extended Search)

melting point of all metallic elements and is used to make filaments for incandescent light bulbs, fluorescent light bulbs and television tubes. Tungsten expands at nearly the...

259

It's Elemental - The Element Darmstadtium  

NLE Websites -- All DOE Office Websites (Extended Search)

Roentgenium The Element Darmstadtium Click for Isotope Data 110 Ds Darmstadtium 281 Atomic Number: 110 Atomic Weight: 281 Melting Point: Unknown Boiling Point: Unknown...

260

It's Elemental - The Element Berkelium  

NLE Websites -- All DOE Office Websites (Extended Search)

Californium The Element Berkelium Click for Isotope Data 97 Bk Berkelium 247 Atomic Number: 97 Atomic Weight: 247 Melting Point: 1323 K (1050C or 1922F) Boiling...

Note: This page contains sample records for the topic "trace elements 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

Method of making a sodium sulfur battery  

SciTech Connect

A method of making a portion of a sodium sulfur battery is disclosed. The battery portion made is a portion of the container which defines the volume for the cathodic reactant materials which are sulfur and sodium polysulfide materials. The container portion is defined by an outer metal casing with a graphite liner contained therein, the graphite liner having a coating on its internal diameter for sealing off the porosity thereof. The steel outer container and graphite pipe are united by a method which insures that at the operating temperature of the battery, relatively low electrical resistance exists between the two materials because they are in intimate contact with one another.

Elkins, Perry E. (Santa Ana, CA)

1981-01-01T23:59:59.000Z

262

Trace 700 | Open Energy Information  

Open Energy Info (EERE)

Trace 700 Trace 700 Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Trace 700 Agency/Company /Organization: Trane Sector: Energy Focus Area: Buildings, Energy Efficiency Topics: Technology characterizations Resource Type: Software/modeling tools Website: www.trane.com/Commercial/Dna/View.aspx?i=1136 References: http://www.trane.com/Commercial/Dna/View.aspx?i=1136 Detailed HVAC design tool. Can provide heating and cooling load calculation, system sizing, and energy use. A fairly thorough understanding of HVAC is necessary to use this tool. Tool Summary LAUNCH TOOL Name: Trace 700 Agency/Company /Organization: Trane Phase: Create a Vision, Determine Baseline, "Evaluate Options and Determine Feasibility" is not in the list of possible values (Bring the Right People Together, Create a Vision, Determine Baseline, Evaluate Options, Develop Goals, Prepare a Plan, Get Feedback, Develop Finance and Implement Projects, Create Early Successes, Evaluate Effectiveness and Revise as Needed) for this property.

263

The trace partitioning abstract domain  

Science Conference Proceedings (OSTI)

In order to achieve better precision of abstract interpretation-based static analysis, we introduce a new generic abstract domain, the trace partitioning abstract domain. We develop a theoretical framework allowing a wide range of instantiations of the ...

Xavier Rival; Laurent Mauborgne

2007-08-01T23:59:59.000Z

264

Encapsulation of mixed radioactive and hazardous waste contaminated incinerator ash in modified sulfur cement  

Science Conference Proceedings (OSTI)

Some of the process waste streams incinerated at various Department of Energy (DOE) facilities contain traces of both low-level radioactive (LLW) and hazardous constituents, thus yielding ash residues that are classified as mixed waste. Work is currently being performed at Brookhaven National Laboratory (BNL) to develop new and innovative materials for encapsulation of DOE mixed wastes including incinerator ash. One such material under investigation is modified sulfur cement, a thermoplastic developed by the US Bureau of Mines. Monolithic waste forms containing as much as 55 wt % incinerator fly ash from Idaho national Engineering Laboratory (INEL) have been formulated with modified sulfur cement, whereas maximum waste loading for this waste in hydraulic cement is 16 wt %. Compressive strength of these waste forms exceeded 27.6 MPa. Wet chemical and solid phase waste characterization analyses performed on this fly ash revealed high concentrations of soluble metal salts including Pb and Cd, identified by the Environmental Protection Agency (EPA) as toxic metals. Leach testing of the ash according to the EPA Toxicity Characteristic Leaching Procedure (TCLP) resulted in concentrations of Pb and Cd above allowable limits. Encapsulation of INEL fly ash in modified sulfur cement with a small quantity of sodium sulfide added to enhance retention of soluble metal salts reduced TCLP leachate concentrations of Pb and Cd well below EPA concentration criteria for delisting as a toxic hazardous waste. 12 refs., 4 figs., 2 tabs.

Kalb, P.D.; Heiser, J.H. III; Colombo, P.

1990-01-01T23:59:59.000Z

265

Low-quality natural gas sulfur removal/recovery  

Science Conference Proceedings (OSTI)

Low quality natural gas processing with the integrated CFZ/CNG Claus process is feasible for low quality natural gas containing 10% or more of CO{sub 2}, and any amount of H{sub 2}S. The CNG Claus process requires a minimum CO{sub 2} partial pressure in the feed gas of about 100 psia (15% CO{sub 2} for a 700 psia feed gas) and also can handle any amount of H{sub 2}S. The process is well suited for handling a variety of trace contaminants usually associated with low quality natural gas and Claus sulfur recovery. The integrated process can produce high pressure carbon dioxide at purities required by end use markets, including food grade CO{sub 2}. The ability to economically co-produce high pressure CO{sub 2} as a commodity with significant revenue potential frees process economic viability from total reliance on pipeline gas, and extends the range of process applicability to low quality gases with relatively low methane content. Gases with high acid gas content and high CO{sub 2} to H{sub 2}S ratios can be economically processed by the CFZ/CNG Claus and CNG Claus processes. The large energy requirements for regeneration make chemical solvent processing prohibitive. The cost of Selexol physical solvent processing of the LaBarge gas is significantly greater than the CNG/CNG Claus and CNG Claus processes.

Damon, D.A. [CNG Research Co., Pittsburgh, PA (United States); Siwajek, L.A. [Acrion Technologies, Inc., Cleveland, OH (United States); Klint, B.W. [BOVAR Inc., AB (Canada). Western Research

1993-12-31T23:59:59.000Z

266

Sulfur, Chlorine, and Argon Abundances in Planetary Nebulae. IV: Synthesis and the Sulfur Anomaly  

E-Print Network (OSTI)

We have compiled a large sample of O, Ne, S, Cl, and Ar abundances which have been determined for 85 galactic planetary nebulae in a consistent and homogeneous manner using spectra extending from 3600-9600 Angstroms. Sulfur abundances have been computed using the near IR lines of [S III] 9069,9532 along with [S III] temperatures. We find average values, expressed logarithmically with a standard deviation, of log(S/O)=-1.91(+/-.24), log(Cl/O)=-3.52(+/-.16), and log(Ar/O)=-2.29(+/-.18), numbers consistent with previous studies of both planetary nebulae and H II regions. We also find a strong correlation between [O III] and [S III] temperatures among planetary nebulae. In analyzing abundances of Ne, S, Cl, and Ar with respect to O, we find a tight correlation for Ne-O, and loose correlations for Cl-O and Ar-O. All three trends appear to be colinear with observed correlations for H II regions. S and O also show a correlation but there is a definite offset from the behavior exhibited by H II regions and stars. We suggest that this S anomaly is most easily explained by the existence of S^+3, whose abundance must be inferred indirectly when only optical spectra are available, in amounts in excess of what is predicted by model-derived ionization correction factors. Finally for the disk PNe, abundances of O, Ne, S, Cl, and Ar all show gradients when plotted against galactocentric distance. The slopes are statistically indistinguishable from one another, a result which is consistent with the notion that the cosmic abundances of these elements evolve in lockstep.

R. B. C. Henry; K. B. Kwitter; Bruce Balick

2004-01-09T23:59:59.000Z

267

Sampling and analysis of natural gas trace constituents  

DOE Green Energy (OSTI)

Major and minor components of natural gas are routinely analyzed by gas chromatography (GC), using a thermal conductivity (TC). The best results obtained by these methods can report no better than 0.01 mole percent of each measured component. Even the extended method of analysis by flame ionization detector (FID) can only improve on the detection limit of hydrocarbons. The gas industry needs better information on all trace constituents of natural gas, whether native or inadvertently added during gas processing that may adversely influence the operation of equipment or the safety of the consumer. The presence of arsenic and mercury in some gas deposits have now been documented in international literature as causing not only human toxicity but also damaging to the field equipment. Yet, no standard methods of sampling and analysis exist to provide this much needed information. In this paper the authors report the results of a three-year program to develop an extensive array of sampling and analysis methods for speciation and measurement of trace constituents of natural gas. A cryogenic sampler operating at near 200 K ({minus}99 F) and at pipeline pressures up to 12.4 {times} 10{sup 6}Pa (1800 psig) has been developed to preconcentrate and recover all trace constituents with boiling points above butanes. Specific analytical methods have been developed for speciating and measurement of many trace components (corresponding to US EPA air toxics) by GC-AED and GC-MS, and for determining various target compounds by other techniques. Moisture, oxygen and sulfur contents are measured on site using dedicated field instruments. Arsenic, mercury and radon are sampled by specific solid sorbents for subsequent laboratory analysis.

Attari, A.; Chao, S.

1993-09-01T23:59:59.000Z

268

Can Sulfur Spectroscopy the Vasa?  

NLE Websites -- All DOE Office Websites (Extended Search)

Title Title by Magnus Sandström*, Farideh Jalilehvand, Ingmar Persson, Ulrik Gelius and Patrick Frank The famous 17th-century Swedish warship Vasa has been on display in the Vasa Museum since 1990 (Figure 1). The Vasa sank on its maiden voyage in 1628, and was recovered in 1961 after 333 years in the cold brackish water of Stockholm harbor. After extensive conservation treatment, the oaken Vasa appeared in good condition (1). Figure 1. The Vasa on display in the Vasa Museum, Stockholm, Sweden. Dimensions: length 61 m (69 m including bowsprit), maximum width 11.7 m, stern castle 19.3 m high, displacement 1210 tons. (photo by Hans Hammarskiöld at the Vasa Museum). Reproduced by permission, (http://www.nature.com/). However, high acidity and a rapid spread of sulfate salts and elemental

269

It's Elemental - The Element Astatine  

NLE Websites -- All DOE Office Websites (Extended Search)

Polonium Polonium Previous Element (Polonium) The Periodic Table of Elements Next Element (Radon) Radon The Element Astatine [Click for Isotope Data] 85 At Astatine 210 Atomic Number: 85 Atomic Weight: 210 Melting Point: 575 K (302°C or 576°F) Boiling Point: Unknown Density: about 7 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Semi-metal Period Number: 6 Group Number: 17 Group Name: Halogen Radioactive What's in a name? From the Greek word for unstable, astatos. Say what? Astatine is pronounced as AS-teh-teen or as AS-teh-ten. History and Uses: Astatine was produced by Dale R. Carson, K.R. MacKenzie and Emilio Segrè by bombarding an isotope of bismuth, bismuth-209, with alpha particles that had been accelerated in a device called a cyclotron. This created

270

It's Elemental - The Element Chromium  

NLE Websites -- All DOE Office Websites (Extended Search)

Vanadium Vanadium Previous Element (Vanadium) The Periodic Table of Elements Next Element (Manganese) Manganese The Element Chromium [Click for Isotope Data] 24 Cr Chromium 51.9961 Atomic Number: 24 Atomic Weight: 51.9961 Melting Point: 2180 K (1907°C or 3465°F) Boiling Point: 2944 K (2671°C or 4840°F) Density: 7.15 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 4 Group Number: 6 Group Name: none What's in a name? From the Greek word for color, chroma. Say what? Chromium is pronounced as KROH-mee-em. History and Uses: Chromium was discovered by Louis-Nicholas Vauquelin while experimenting with a material known as Siberian red lead, also known as the mineral crocoite (PbCrO4), in 1797. He produced chromium oxide (CrO3) by mixing

271

It's Elemental - The Element Iron  

NLE Websites -- All DOE Office Websites (Extended Search)

Manganese Manganese Previous Element (Manganese) The Periodic Table of Elements Next Element (Cobalt) Cobalt The Element Iron [Click for Isotope Data] 26 Fe Iron 55.845 Atomic Number: 26 Atomic Weight: 55.845 Melting Point: 1811 K (1538°C or 2800°F) Boiling Point: 3134 K (2861°C or 5182°F) Density: 7.874 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 4 Group Number: 8 Group Name: none What's in a name? From the Anglo-Saxon word iron. Iron's chemical symbol comes from the Latin word for iron, ferrum. Say what? Iron is pronounced as EYE-ern. History and Uses: Archaeological evidence suggests that people have been using iron for at least 5000 years. Iron is the cheapest and one of the most abundant of all metals, comprising nearly 5.6% of the earth's crust and nearly all of the

272

It's Elemental - The Element Molybdenum  

NLE Websites -- All DOE Office Websites (Extended Search)

Niobium Niobium Previous Element (Niobium) The Periodic Table of Elements Next Element (Technetium) Technetium The Element Molybdenum [Click for Isotope Data] 42 Mo Molybdenum 95.96 Atomic Number: 42 Atomic Weight: 95.96 Melting Point: 2896 K (2623°C or 4753°F) Boiling Point: 4912 K (4639°C or 8382°F) Density: 10.2 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 5 Group Number: 6 Group Name: none What's in a name? From the Greek word for lead, molybdos. Say what? Molybdenum is pronounced as meh-LIB-deh-nem. History and Uses: Molybdenum was discovered by Carl Welhelm Scheele, a Swedish chemist, in 1778 in a mineral known as molybdenite (MoS2) which had been confused as a lead compound. Molybdenum was isolated by Peter Jacob Hjelm in 1781. Today,

273

It's Elemental - The Element Cesium  

NLE Websites -- All DOE Office Websites (Extended Search)

Xenon Xenon Previous Element (Xenon) The Periodic Table of Elements Next Element (Barium) Barium The Element Cesium [Click for Isotope Data] 55 Cs Cesium 132.9054519 Atomic Number: 55 Atomic Weight: 132.9054519 Melting Point: 301.59 K (28.44°C or 83.19°F) Boiling Point: 944 K (671°C or 1240°F) Density: 1.93 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: 1 Group Name: Alkali Metal What's in a name? From the Latin word for sky blue, caesius. Say what? Cesium is pronounced as SEE-zee-em. History and Uses: Cesium was discovered by Robert Wilhelm Bunsen and Gustav Robert Kirchhoff, German chemists, in 1860 through the spectroscopic analysis of Durkheim mineral water. They named cesium after the blue lines they observed in its

274

It's Elemental - The Element Iridium  

NLE Websites -- All DOE Office Websites (Extended Search)

Osmium Osmium Previous Element (Osmium) The Periodic Table of Elements Next Element (Platinum) Platinum The Element Iridium [Click for Isotope Data] 77 Ir Iridium 192.217 Atomic Number: 77 Atomic Weight: 192.217 Melting Point: 2719 K (2446°C or 4435°F) Boiling Point: 4701 K (4428°C or 8002°F) Density: 22.42 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: 9 Group Name: none What's in a name? From the Latin word for rainbow, iris. Say what? Iridium is pronounced as i-RID-ee-em. History and Uses: Iridium and osmium were discovered at the same time by the British chemist Smithson Tennant in 1803. Iridium and osmium were identified in the black residue remaining after dissolving platinum ore with aqua regia, a mixture

275

It's Elemental - The Element Platinum  

NLE Websites -- All DOE Office Websites (Extended Search)

Iridium Iridium Previous Element (Iridium) The Periodic Table of Elements Next Element (Gold) Gold The Element Platinum [Click for Isotope Data] 78 Pt Platinum 195.084 Atomic Number: 78 Atomic Weight: 195.084 Melting Point: 2041.55 K (1768.4°C or 3215.1°F) Boiling Point: 4098 K (3825°C or 6917°F) Density: 21.46 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: 10 Group Name: none What's in a name? From the Spainsh word for silver, platina. Say what? Platinum is pronounced as PLAT-en-em. History and Uses: Used by the pre-Columbian Indians of South America, platinum wasn't noticed by western scientists until 1735. Platinum can occur free in nature and is sometimes found in deposits of gold-bearing sands, primarily those found in

276

It's Elemental - The Element Arsenic  

NLE Websites -- All DOE Office Websites (Extended Search)

Germanium Germanium Previous Element (Germanium) The Periodic Table of Elements Next Element (Selenium) Selenium The Element Arsenic [Click for Isotope Data] 33 As Arsenic 74.92160 Atomic Number: 33 Atomic Weight: 74.92160 Melting Point: 1090 K (817°C or 1503°F) Boiling Point: 887 K (614°C or 1137°F) Density: 5.776 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Semi-metal Period Number: 4 Group Number: 15 Group Name: Pnictogen What's in a name? From the Latin word arsenicum, the Greek word arsenikon and the Arabic word Az-zernikh. Say what? Arsenic is pronounced as AR-s'n-ik. History and Uses: Although arsenic compounds were mined by the early Chinese, Greek and Egyptian civilizations, it is believed that arsenic itself was first identified by Albertus Magnus, a German alchemist, in 1250. Arsenic occurs

277

It's Elemental - The Element Barium  

NLE Websites -- All DOE Office Websites (Extended Search)

Cesium Cesium Previous Element (Cesium) The Periodic Table of Elements Next Element (Lanthanum) Lanthanum The Element Barium [Click for Isotope Data] 56 Ba Barium 137.327 Atomic Number: 56 Atomic Weight: 137.327 Melting Point: 1000 K (727°C or 1341°F) Boiling Point: 2170 K (1897°C or 3447°F) Density: 3.62 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: 2 Group Name: Alkaline Earth Metal What's in a name? From the Greek word for heavy, barys. Say what? Barium is pronounced as BAR-ee-em. History and Uses: Barium was first isolated by Sir Humphry Davy, an English chemist, in 1808 through the electrolysis of molten baryta (BaO). Barium is never found free in nature since it reacts with oxygen in the air, forming barium oxide

278

It's Elemental - The Element Gold  

NLE Websites -- All DOE Office Websites (Extended Search)

Platinum Platinum Previous Element (Platinum) The Periodic Table of Elements Next Element (Mercury) Mercury The Element Gold [Click for Isotope Data] 79 Au Gold 196.966569 Atomic Number: 79 Atomic Weight: 196.966569 Melting Point: 1337.33 K (1064.18°C or 1947.52°F) Boiling Point: 3129 K (2856°C or 5173°F) Density: 19.282 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: 11 Group Name: none What's in a name? From the Sanskrit word Jval and the Anglo-Saxon word gold. Gold's chemical symbol comes from the the latin word for gold, aurum. Say what? Gold is pronounced as GOLD. History and Uses: An attractive and highly valued metal, gold has been known for at least 5500 years. Gold is sometimes found free in nature but it is usually found

279

It's Elemental - The Element Rhenium  

NLE Websites -- All DOE Office Websites (Extended Search)

Tungsten Tungsten Previous Element (Tungsten) The Periodic Table of Elements Next Element (Osmium) Osmium The Element Rhenium [Click for Isotope Data] 75 Re Rhenium 186.207 Atomic Number: 75 Atomic Weight: 186.207 Melting Point: 3459 K (3186°C or 5767°F) Boiling Point: 5869 K (5596°C or 10105°F) Density: 20.8 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: 7 Group Name: none What's in a name? From the Latin word for the Rhine River, Rhenus. Say what? Rhenium is pronounced as REE-nee-em. History and Uses: Rhenium was discovered by the German chemists Ida Tacke-Noddack, Walter Noddack and Otto Carl Berg in 1925. They detected rhenium spectroscopically in platinum ores and in the minerals columbite ((Fe, Mn, Mg)(Nb, Ta)2O6),

280

It's Elemental - The Element Copper  

NLE Websites -- All DOE Office Websites (Extended Search)

Nickel Nickel Previous Element (Nickel) The Periodic Table of Elements Next Element (Zinc) Zinc The Element Copper [Click for Isotope Data] 29 Cu Copper 63.546 Atomic Number: 29 Atomic Weight: 63.546 Melting Point: 1357.77 K (1084.62°C or 1984.32°F) Boiling Point: 2835 K (2562°C or 4644°F) Density: 8.933 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 4 Group Number: 11 Group Name: none What's in a name? From the Latin word cuprum, which means "from the island of Cyprus." Say what? Copper is pronounced as KOP-er. History and Uses: Archaeological evidence suggests that people have been using copper for at least 11,000 years. Relatively easy to mine and refine, people discovered methods for extracting copper from its ores at least 7,000 years ago. The

Note: This page contains sample records for the topic "trace elements 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

It's Elemental - The Element Gadolinium  

NLE Websites -- All DOE Office Websites (Extended Search)

Europium Europium Previous Element (Europium) The Periodic Table of Elements Next Element (Terbium) Terbium The Element Gadolinium [Click for Isotope Data] 64 Gd Gadolinium 157.25 Atomic Number: 64 Atomic Weight: 157.25 Melting Point: 1586 K (1313°C or 2395°F) Boiling Point: 3546 K (3273°C or 5923°F) Density: 7.90 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: none Group Name: Lanthanide What's in a name? Named for the mineral gadolinite which was named after Johan Gadolin, a Finnish chemist. Say what? Gadolinium is pronounced as GAD-oh-LIN-ee-em. History and Uses: Spectroscopic evidence for the existence of gadolinium was first observed by the Swiss chemist Jean Charles Galissard de Marignac in the minerals

282

It's Elemental - The Element Mercury  

NLE Websites -- All DOE Office Websites (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

283

It's Elemental - The Element Hafnium  

NLE Websites -- All DOE Office Websites (Extended Search)

Lutetium Lutetium Previous Element (Lutetium) The Periodic Table of Elements Next Element (Tantalum) Tantalum The Element Hafnium [Click for Isotope Data] 72 Hf Hafnium 178.49 Atomic Number: 72 Atomic Weight: 178.49 Melting Point: 2506 K (2233°C or 4051°F) Boiling Point: 4876 K (4603°C or 8317°F) Density: 13.3 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: 4 Group Name: none What's in a name? From the Latin word for the city of Copenhagen, Hafnia. Say what? Hafnium is pronounced as HAF-neeem. History and Uses: Hafnium was discovered by Dirk Coster, a Danish chemist, and Charles de Hevesy, a Hungarian chemist, in 1923. They used a method known as X-ray spectroscopy to study the arrangement of the outer electrons of atoms in

284

It's Elemental - The Element Boron  

NLE Websites -- All DOE Office Websites (Extended Search)

Beryllium Beryllium Previous Element (Beryllium) The Periodic Table of Elements Next Element (Carbon) Carbon The Element Boron [Click for Isotope Data] 5 B Boron 10.811 Atomic Number: 5 Atomic Weight: 10.811 Melting Point: 2348 K (2075°C or 3767°F) Boiling Point: 4273 K (4000°C or 7232°F) Density: 2.37 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Semi-metal Period Number: 2 Group Number: 13 Group Name: none What's in a name? From the Arabic word Buraq and the Persian word Burah, which are both words for the material "borax." Say what? Boron is pronounced as BO-ron. History and Uses: Boron was discovered by Joseph-Louis Gay-Lussac and Louis-Jaques Thénard, French chemists, and independently by Sir Humphry Davy, an English chemist,

285

It's Elemental - The Element Thorium  

NLE Websites -- All DOE Office Websites (Extended Search)

Actinium Actinium Previous Element (Actinium) The Periodic Table of Elements Next Element (Protactinium) Protactinium The Element Thorium [Click for Isotope Data] 90 Th Thorium 232.03806 Atomic Number: 90 Atomic Weight: 232.03806 Melting Point: 2023 K (1750°C or 3182°F) Boiling Point: 5061 K (4788°C or 8650°F) Density: 11.72 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 7 Group Number: none Group Name: Actinide Radioactive What's in a name? Named for the Scandinavian god of war, Thor. Say what? Thorium is pronounced as THOR-ee-em or as THO-ree-em. History and Uses: Thorium was discovered by Jöns Jacob Berzelius, a Swedish chemist, in 1828. He discovered it in a sample of a mineral that was given to him by the Reverend Has Morten Thrane Esmark, who suspected that it contained an

286

It's Elemental - The Element Osmium  

NLE Websites -- All DOE Office Websites (Extended Search)

Rhenium Rhenium Previous Element (Rhenium) The Periodic Table of Elements Next Element (Iridium) Iridium The Element Osmium [Click for Isotope Data] 76 Os Osmium 190.23 Atomic Number: 76 Atomic Weight: 190.23 Melting Point: 3306 K (3033°C or 5491°F) Boiling Point: 5285 K (5012°C or 9054°F) Density: 22.57 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: 8 Group Name: none What's in a name? From the Greek word for a smell, osme. Say what? Osmium is pronounced as OZ-mee-em. History and Uses: Osmium and iridium were discovered at the same time by the British chemist Smithson Tennant in 1803. Osmium and iridium were identified in the black residue remaining after dissolving platinum ore with aqua regia, a mixture

287

It's Elemental - The Element Antimony  

NLE Websites -- All DOE Office Websites (Extended Search)

Tin Tin Previous Element (Tin) The Periodic Table of Elements Next Element (Tellurium) Tellurium The Element Antimony [Click for Isotope Data] 51 Sb Antimony 121.760 Atomic Number: 51 Atomic Weight: 121.760 Melting Point: 903.78 K (630.63°C or 1167.13°F) Boiling Point: 1860 K (1587°C or 2889°F) Density: 6.685 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Semi-metal Period Number: 5 Group Number: 15 Group Name: Pnictogen What's in a name? From the Greek words anti and monos, which together mean "not alone." Antimony's chemical symbol comes from its historic name, Stibium. Say what? Antimony is pronounced as AN-the-MOH-nee. History and Uses: Antimony has been known since ancient times. It is sometimes found free in nature, but is usually obtained from the ores stibnite (Sb2S3) and

288

Sulfur in the Timbers of Henry VIII's Warship Mary Rose: Synchrotrons  

NLE Websites -- All DOE Office Websites (Extended Search)

Sulfur in the Timbers of Henry Sulfur in the Timbers of Henry VIII's Warship Mary Rose: Synchrotrons Illuminate Conservation Concerns Magnus Sandström,1 Farideh Jalilehvand,2 Emiliana Damian,1 Yvonne Fors,1 Ulrik Gelius,3 Mark Jones,4 and Murielle Salomé5 1Structural Chemistry, Stockholm University, Sweden 2Department of Chemistry, University of Calgary, Alberta, Canada 3Department of Physics, Uppsala University, Sweden 4The Mary Rose Trust, HM Naval Base, Portsmouth, UK 5European Synchrotron Radiation Facility (ESRF), Grenoble, France Figure 1.The starboard side of the Mary Rose (about ½ of the hull, ~280 tons oak timbers) is since 1994 being sprayed with an aqueous solution of PEG 200. Figure 2. Sulfur K-edge XANES spectrum of Mary Rose oak core surface (0-3 mm). Standard spectra used for model fitting: 1 (solution), 1' (solid) disulfides R-SS-R (cystine with peaks at 2472.7 and 2474.4 eV); 45%; 2: Thiols R-SH (cysteine, 2473.6 eV) 23%; 3: Elemental sulfur (S8 in xylene 2473.0 eV) 10%; 4: Sulfoxide R(SO)R' (methionine sulfoxide, 2476.4 eV) 5%; 5: Sulfonate R-SO3- (methyl sulfonate, 2481.2 eV) 10%; 6: Sulfate SO42- (sodium sulfate, 2482.6 eV) 7%.

289

Sulfuric acid thermoelectrochemical system and method  

DOE Patents (OSTI)

A thermoelectrochemical system in which an electrical current is generated between a cathode immersed in a concentrated sulfuric acid solution and an anode immersed in an aqueous buffer solution of sodium bisulfate and sodium sulfate. Reactants consumed at the electrodes during the electrochemical reaction are thermochemically regenerated and recycled to the electrodes to provide continuous operation of the system.

Ludwig, Frank A. (Rancho Palos Verdes, CA)

1989-01-01T23:59:59.000Z

290

Reducing Sulfur Hexafluoride Use at LANSCE  

NLE Websites -- All DOE Office Websites (Extended Search)

U N C L A S S I F I E D U N C L A S S I F I E D Reducing Sulfur Hexafluoride Use at LANSCE Hank Alvestad presents to the Fugitive Emissions Working Group September 8, 2011...

291

Process for removing sulfur from sulfur-containing gases: high calcium fly-ash  

DOE Patents (OSTI)

The present disclosure relates to improved processes for treating hot sulfur-containing flue gas to remove sulfur therefrom. Processes in accordance with the present invention include preparing an aqueous slurry composed of a calcium alkali source and a source of reactive silica and/or alumina, heating the slurry to above-ambient temperatures for a period of time in order to facilitate the formation of sulfur-absorbing calcium silicates or aluminates, and treating the gas with the heat-treated slurry components. Examples disclosed herein demonstrate the utility of these processes in achieving improved sulfur-absorbing capabilities. Additionally, disclosure is provided which illustrates preferred configurations for employing the present processes both as a dry sorbent injection and for use in conjunction with a spray dryer and/or bagfilter. Retrofit application to existing systems is also addressed.

Rochelle, Gary T. (Austin, TX); Chang, John C. S. (Cary, NC)

1991-01-01T23:59:59.000Z

292

Apparatus and Method for Ultra-Sensitive trace Analysis  

DOE Patents (OSTI)

An apparatus and method for conducting ultra-sensitive trace element and isotope analysis. The apparatus injects a sample through a fine nozzle to form an atomic beam. A DC discharge is used to elevate select atoms to a metastable energy level. These atoms are then acted on by a laser oriented orthogonally to the beam path to reduce the traverse velocity and to decrease the divergence angle of the beam. The beam then enters a Zeeman slower where a counter-propagating laser beam acts to slow the atoms down. Then select atoms are captured in a magneto-optical trap where they undergo fluorescence. A portion of the scattered photons are imaged onto a photo-detector, and the results analyzed to detect the presence of single atoms of the specific trace elements.

Lu, Zhengtian; Bailey, Kevin G.; Chen, Chun Yen; Li, Yimin; O' Connor, Thomas P.; Young, Linda

2000-01-03T23:59:59.000Z

293

The role of trace gas flux networks in biogeosciences  

SciTech Connect

Vast networks of meteorological sensors ring the globe, providing continuous measurements of an array of atmospheric state variables such as temperature, humidity, rainfall, and the concentration of carbon dioxide [New etal., 1999; Tans etal., 1996]. These measurements provide input to weather and climate models and are key to detecting trends in climate, greenhouse gases, and air pollution. Yet to understand how and why these atmospheric state variables vary in time and space, biogeoscientists need to know where, when, and at what rates important gases are flowing between the land and the atmosphere. Tracking trace gas fluxes provides information on plant or microbial metabolism and climate-ecosystem interactions. The existence of trace gas flux networks is a relatively new phenomenon, dating back to research in 1984. The first gas flux measurement networks were regional in scope and were designed to track pollutant gases such as sulfur dioxide, ozone, nitric acid, and nitrogen dioxide. Atmospheric observations and model simulations were used to infer the depositional rates of these hazardous chemicals [Fowler etal., 2009; Meyers etal., 1991]. In the late 1990s, two additional trace gas flux measurement networks emerged. One, the United States Trace Gas Network (TRAGNET), was a short-lived effort that measured trace gas emissions from the soil and plants with chambers distributed throughout the country [Ojima etal., 2000]. The other, FLUXNET, was an international endeavor that brought many regional networks together to measure the fluxes of carbon dioxide, water vapor, and sensible heat exchange with the eddy covariance technique [Baldocchi etal., 2001]. FLUXNET, which remains active today, currently includes more than 400 tower sites, dispersed across most of the world's climatic zones and biomes, with sites in North and South America, Europe, Asia, Africa, and Australia. More recently, several specialized networks have emerged, including networks dedicated to urban areas (Urban Fluxnet), nitrogen compounds in Europe (NitroEurope), and methane (MethaneNet). Technical Aspects of Flux Networks Eddy covariance flux measurements are the preferred method by which biogeoscientists measure trace gas exchange between ecosystems and the atmosphere [Baldocchi, 2003].

Baldocch, Dennis [Department of Environmental Science, Policy and Management, University of California, Berkeley,; Reichstein, Markus [Max Planck Institute for Biogeochemistry; Papale, D. [University of Tuscia; KOTEEN, LAURIE [University of California, Berkeley; VARGAS, RODRIGO [Ensenada Center for Scientific Research and Higher Education (CICESE); Agarwal, D.A [Lawrence Berkeley National Laboratory (LBNL); Cook, Robert B [ORNL

2012-01-01T23:59:59.000Z

294

CATALYST EVALUATION FOR A SULFUR DIOXIDE-DEPOLARIZED ELECTROLYZER  

DOE Green Energy (OSTI)

Thermochemical processes are being developed to provide global-scale quantities of hydrogen. A variant on sulfur-based thermochemical cycles is the Hybrid Sulfur (HyS) Process which uses a sulfur dioxide depolarized electrolyzer (SDE) to produce the hydrogen. Testing examined the activity and stability of platinum and palladium as the electrocatalyst for the SDE in sulfuric acid solutions. Cyclic and linear sweep voltammetry revealed that platinum provided better catalytic activity with much lower potentials and higher currents than palladium. Testing also showed that the catalyst activity is strongly influenced by the concentration of the sulfuric acid electrolyte.

Hobbs, D; Hector Colon-Mercado, H

2007-01-31T23:59:59.000Z

295

It's Elemental - The Element Promethium  

NLE Websites -- All DOE Office Websites (Extended Search)

(Samarium) Samarium The Element Promethium Click for Isotope Data 61 Pm Promethium 145 Atomic Number: 61 Atomic Weight: 145 Melting Point: 1315 K (1042C or 1908F) Boiling...

296

It's Elemental - The Element Cadmium  

NLE Websites -- All DOE Office Websites (Extended Search)

(Indium) Indium The Element Cadmium Click for Isotope Data 48 Cd Cadmium 112.411 Atomic Number: 48 Atomic Weight: 112.411 Melting Point: 594.22 K (321.07C or 609.93F)...

297

It's Elemental - The Element Praseodymium  

NLE Websites -- All DOE Office Websites (Extended Search)

Today, praseodymium is primarily obtained through an ion exchange process from monazite sand ((Ce, La, Th, Nd, Y)PO4), a material rich in rare earth elements. Praseodymium's...

298

It's Elemental - The Element Neodymium  

NLE Websites -- All DOE Office Websites (Extended Search)

Today, neodymium is primarily obtained from through an ion exchange process monazite sand ((Ce, La, Th, Nd, Y)PO4), a material rich in rare earth elements. Neodymium makes up...

299

It's Elemental - The Element Samarium  

NLE Websites -- All DOE Office Websites (Extended Search)

1879. Today, samarium is primarily obtained through an ion exchange process from monazite sand ((Ce, La, Th, Nd, Y)PO4), a material rich in rare earth elements that can contain as...

300

It's Elemental - The Element Lanthanum  

NLE Websites -- All DOE Office Websites (Extended Search)

Today, lanthanum is primarily obtained through an ion exchange process from monazite sand ((Ce, La, Th, Nd, Y)PO4), a material rich in rare earth elements that can contain as...

Note: This page contains sample records for the topic "trace elements 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

It's Elemental - The Element Lutetium  

NLE Websites -- All DOE Office Websites (Extended Search)

(Hafnium) Hafnium The Element Lutetium Click for Isotope Data 71 Lu Lutetium 174.9668 Atomic Number: 71 Atomic Weight: 174.9668 Melting Point: 1936 K (1663C or 3025F)...

302

It's Elemental - The Element Holmium  

NLE Websites -- All DOE Office Websites (Extended Search)

(Erbium) Erbium The Element Holmium Click for Isotope Data 67 Ho Holmium 164.93032 Atomic Number: 67 Atomic Weight: 164.93032 Melting Point: 1747 K (1474C or 2685F)...

303

It's Elemental - The Element Zinc  

NLE Websites -- All DOE Office Websites (Extended Search)

Copper Copper Previous Element (Copper) The Periodic Table of Elements Next Element (Gallium) Gallium The Element Zinc [Click for Isotope Data] 30 Zn Zinc 65.38 Atomic Number: 30 Atomic Weight: 65.38 Melting Point: 692.68 K (419.53°C or 787.15°F) Boiling Point: 1180 K (907°C or 1665°F) Density: 7.134 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 4 Group Number: 12 Group Name: none What's in a name? From the German word zink. Say what? Zinc is pronounced as ZINK. History and Uses: Although zinc compounds have been used for at least 2,500 years in the production of brass, zinc wasn't recognized as a distinct element until much later. Metallic zinc was first produced in India sometime in the 1400s by heating the mineral calamine (ZnCO3) with wool. Zinc was rediscovered by

304

It's Elemental - The Element Fluorine  

NLE Websites -- All DOE Office Websites (Extended Search)

Oxygen Oxygen Previous Element (Oxygen) The Periodic Table of Elements Next Element (Neon) Neon The Element Fluorine [Click for Isotope Data] 9 F Fluorine 18.9984032 Atomic Number: 9 Atomic Weight: 18.9984032 Melting Point: 53.53 K (-219.62°C or -363.32°F) Boiling Point: 85.03 K (-188.12°C or -306.62°F) Density: 0.001696 grams per cubic centimeter Phase at Room Temperature: Gas Element Classification: Non-metal Period Number: 2 Group Number: 17 Group Name: Halogen What's in a name? From the Latin and French words for flow, fluere. Say what? Fluorine is pronounced as FLU-eh-reen or as FLU-eh-rin. History and Uses: Fluorine is the most reactive of all elements and no chemical substance is capable of freeing fluorine from any of its compounds. For this reason, fluorine does not occur free in nature and was extremely difficult for

305

FUEL ELEMENT  

DOE Patents (OSTI)

A ceramic fuel element for a nuclear reactor that has improved structural stability as well as improved cooling and fission product retention characteristics is presented. The fuel element includes a plurality of stacked hollow ceramic moderator blocks arranged along a tubular raetallic shroud that encloses a series of axially apertured moderator cylinders spaced inwardly of the shroud. A plurality of ceramic nuclear fuel rods are arranged in the annular space between the shroud and cylinders of moderator and appropriate support means and means for directing gas coolant through the annular space are also provided. (AEC)

Bean, R.W.

1963-11-19T23:59:59.000Z

306

It's Elemental - Isotopes of the Element Thorium  

NLE Websites -- All DOE Office Websites (Extended Search)

Table of Elements Next Element (Protactinium) Protactinium Isotopes of the Element Thorium Click for Main Data Most of the isotope data on this site has been obtained from...

307

It's Elemental - The Element Lead  

NLE Websites -- All DOE Office Websites (Extended Search)

Thallium Thallium Previous Element (Thallium) The Periodic Table of Elements Next Element (Bismuth) Bismuth The Element Lead [Click for Isotope Data] 82 Pb Lead 207.2 Atomic Number: 82 Atomic Weight: 207.2 Melting Point: 600.61 K (327.46°C or 621.43°F) Boiling Point: 2022 K (1749°C or 3180°F) Density: 11.342 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Metal Period Number: 6 Group Number: 14 Group Name: none What's in a name? From the Anglo-Saxon word lead. Lead's chemical symbol comes from the Latin word for waterworks, plumbum. Say what? Lead is pronounced as LED. History and Uses: Lead has been known since ancient times. It is sometimes found free in nature, but is usually obtained from the ores galena (PbS), anglesite (PbSO4), cerussite (PbCO3) and minum (Pb3O4). Although lead makes up only

308

sulfur dioxide emissions | OpenEI  

Open Energy Info (EERE)

sulfur dioxide emissions sulfur dioxide emissions Dataset Summary Description Emissions from energy use in buildings are usually estimated on an annual basis using annual average multipliers. Using annual numbers provides a reasonable estimation of emissions, but it provides no indication of the temporal nature of the emissions. Therefore, there is no way of understanding the impact on emissions from load shifting and peak shaving technologies such as thermal energy storage, on-site renewable energy, and demand control. Source NREL Date Released April 11th, 2011 (3 years ago) Date Updated April 11th, 2011 (3 years ago) Keywords buildings carbon dioxide emissions carbon footprinting CO2 commercial buildings electricity emission factors ERCOT hourly emission factors interconnect nitrogen oxides

309

Chlorine and Sulfur in Nearby Planetary Nebulae and H II Regions  

E-Print Network (OSTI)

We derive the chlorine abundances in a sample of nearby planetary nebulae (PNe) and H II regions that have some of the best available spectra. We use a nearly homogeneous procedure to derive the abundance in each object and find that the Cl/H abundance ratio shows similar values in H II regions and PNe. This supports our previous interpretation that the underabundance we found for oxygen in the H II regions is due to the depletion of their oxygen atoms into organic refractory dust components. For other elements, the bias introduced by ionization correction factors in their derived abundances can be very important, as we illustrate here for sulfur using photoionization models. Even for low-ionization PNe, the derived sulfur abundances can be lower than the real ones by up to 0.3 dex, and the differences found with the abundances derived for H II regions that have similar S/H can reach 0.4 dex.

Rodrguez, Mnica

2011-01-01T23:59:59.000Z

310

Complete genome sequence of the sulfur compounds oxidizing chemolithoautotroph Sulfuricurvum kujiense type strain (YK-1T)  

SciTech Connect

Sulfuricurvum kujiense Kodama and Watanabe 2004 is the type species of the monotypic genus Sulfuricurvum, which belongs to the family Helicobacteriaceae in the class Epsilonproteobacteria. The species is of interest because it is frequently found in crude oil and oil sands where it utilizes various reduced sulfur compounds such as elemental sulfur, sulfide and thiosulfate as electron donors. Members of the species do not utilize sugars, organic acids and hydrocarbons as carbon and energy sources. This is the first completed genome sequence of a member of the genus Sulfuricurvum. The genome, which consists of a circular chromosome of 2,574,824 bp length and four plasmids of 118,585 bp, 71,513 bp, 51,014 bp, and 3,421 bp length, respectively, harboring a total of 2,879 protein-coding and 61 RNA genes and is a part of the Genomic Encyclopedia of Bacteria and Archaea project.

Han, Cliff [Los Alamos National Laboratory (LANL); Kotsyurbenko, Oleg [Technical University of Braunschweig; Chertkov, Olga [Los Alamos National Laboratory (LANL); Held, Brittany [Los Alamos National Laboratory (LANL); Lapidus, Alla L. [U.S. Department of Energy, Joint Genome Institute; Nolan, Matt [U.S. Department of Energy, Joint Genome Institute; Lucas, Susan [U.S. Department of Energy, Joint Genome Institute; Hammon, Nancy [U.S. Department of Energy, Joint Genome Institute; Deshpande, Shweta [U.S. Department of Energy, Joint Genome Institute; Cheng, Jan-Fang [U.S. Department of Energy, Joint Genome Institute; Tapia, Roxanne [Los Alamos National Laboratory (LANL); Goodwin, Lynne A. [Los Alamos National Laboratory (LANL); Pitluck, Sam [U.S. Department of Energy, Joint Genome Institute; Liolios, Konstantinos [U.S. Department of Energy, Joint Genome Institute; Pagani, Ioanna [U.S. Department of Energy, Joint Genome Institute; Ivanova, N [U.S. Department of Energy, Joint Genome Institute; Mavromatis, K [U.S. Department of Energy, Joint Genome Institute; Mikhailova, Natalia [U.S. Department of Energy, Joint Genome Institute; Pati, Amrita [U.S. Department of Energy, Joint Genome Institute; Chen, Amy [U.S. Department of Energy, Joint Genome Institute; Palaniappan, Krishna [U.S. Department of Energy, Joint Genome Institute; Land, Miriam L [ORNL; Hauser, Loren John [ORNL; Chang, Yun-Juan [ORNL; Jeffries, Cynthia [Oak Ridge National Laboratory (ORNL); Brambilla, Evelyne-Marie [DSMZ - German Collection of Microorganisms and Cell Cultures GmbH, Braunschweig, Germany; Rohde, Manfred [HZI - Helmholtz Centre for Infection Research, Braunschweig, Germany; Spring, Stefan [DSMZ - German Collection of Microorganisms and Cell Cultures GmbH, Braunschweig, Germany; Sikorski, Johannes [DSMZ - German Collection of Microorganisms and Cell Cultures GmbH, Braunschweig, Germany; Goker, Markus [DSMZ - German Collection of Microorganisms and Cell Cultures GmbH, Braunschweig, Germany; Woyke, Tanja [U.S. Department of Energy, Joint Genome Institute; Bristow, James [U.S. Department of Energy, Joint Genome Institute; Eisen, Jonathan [U.S. Department of Energy, Joint Genome Institute; Markowitz, Victor [U.S. Department of Energy, Joint Genome Institute; Hugenholtz, Philip [U.S. Department of Energy, Joint Genome Institute; Kyrpides, Nikos C [U.S. Department of Energy, Joint Genome Institute; Klenk, Hans-Peter [DSMZ - German Collection of Microorganisms and Cell Cultures GmbH, Braunschweig, Germany; Detter, J. Chris [U.S. Department of Energy, Joint Genome Institute

2012-01-01T23:59:59.000Z

311

Trace Metal Source Terms in Carbon Sequestration Environments  

Science Conference Proceedings (OSTI)

ABSTRACT: Carbon dioxide sequestration in deep saline and depleted oil geologic formations is feasible and promising; however, possible CO2 or CO2-saturated brine leakage to overlying aquifers may pose environmental and health impacts. The purpose of this study was to experimentally define to provide a range of concentrations that can be used as the trace element source term for reservoirs and leakage pathways in risk simulations. Storage source terms for trace metals are needed to evaluate the impact of brines leaking into overlying drinking water aquifers. The trace metal release was measured from cements and sandstones, shales, carbonates, evaporites, and basalts from the Frio, In Salah, Illinois Basin, Decatur, Lower Tuscaloosa, Weyburn-Midale, Bass Islands, and Grand Ronde carbon sequestration geologic formations. Trace metal dissolution was tracked by measuring solution concentrations over time under conditions (e.g., pressures, temperatures, and initial brine compositions) specific to the sequestration projects. Existing metrics for maximum contaminant levels (MCLs) for drinking water as defined by the U.S. Environmental Protection Agency (U.S. EPA) were used to categorize the relative significance of metal concentration changes in storage environments because of the presence of CO2. Results indicate that Cr and Pb released from sandstone reservoir and shale cap rocks exceed the MCLs byan order of magnitude, while Cd and Cu were at or below drinking water thresholds. In carbonate reservoirs As exceeds the MCLs by an order of magnitude, while Cd, Cu, and Pb were at or below drinking water standards. Results from this study can be used as a reasonable estimate of the trace element source term for reservoirs and leakage pathways in risk simulations to further evaluate the impact of leakage on groundwater quality.

Karamalidis, Athanasios; Torres, Sharon G.; Hakala, Jacqueline A.; Shao, Hongbo; Cantrell, Kirk J.; Carroll, Susan A.

2013-01-01T23:59:59.000Z

312

Base Elements  

Science Conference Proceedings (OSTI)

Table 4   Principal effects of superalloy base elements on alloy characteristics...to γ? or γ? Requires fcc stabilizer Cobalt prices have been known to be volatile in the past. Suitable for creep-resistant applications with low stresses or

313

Treatability study on the use of by-product sulfur in Kazakhstan for the stabilization of hazardous and radioactive wastes  

SciTech Connect

The Republic of Kazakhstan generates significant quantities of excess sulfur from the production and refining of petroleum reserves. In addition, the country also produces hazardous, and radioactive wastes which require treatment/stabilization. In an effort to find secondary uses for the elemental sulfur, and simultaneously produce a material which could be used to encapsulate, and reduce the dispersion of harmful contaminants into the environment, BNL evaluated the use of the sulfur polymer cement (SPC) produced from by-product sulfur in Kazakhstan. This thermoplastic binder material forms a durable waste form with low leaching properties and is compatible with a wide range of waste types. Several hundred kilograms of Kazakhstan sulfur were shipped to the U.S. and converted to SPC (by reaction with 5 wt% organic modifiers) for use in this study. A phosphogypsum sand waste generated in Kazakhstan during the purification of phosphate fertilizer was selected for treatment. Waste loading of 40 wt% were easily achieved. Waste form performance testing included compressive strength, water immersion, and Accelerated Leach Testing. 14 refs., 7 figs., 6 tabs.

Yim, Sung Paal; Kalb, P.D.; Milian, L.W.

1997-08-01T23:59:59.000Z

314

Development of the Hybrid Sulfur Thermochemical Cycle  

DOE Green Energy (OSTI)

The production of hydrogen via the thermochemical splitting of water is being considered as a primary means for utilizing the heat from advanced nuclear reactors to provide fuel for a hydrogen economy. The Hybrid Sulfur (HyS) Process is one of the baseline candidates identified by the U.S. Department of Energy [1] for this purpose. The HyS Process is a two-step hybrid thermochemical cycle that only involves sulfur, oxygen and hydrogen compounds. Recent work has resulted in an improved process design with a calculated overall thermal efficiency (nuclear heat to hydrogen, higher heating value basis) approaching 50%. Economic analyses indicate that a nuclear hydrogen plant employing the HyS Process in conjunction with an advanced gas-cooled nuclear reactor system can produce hydrogen at competitive prices. Experimental work has begun on the sulfur dioxide depolarized electrolyzer, the major developmental component in the cycle. Proof-of-concept tests have established proton-exchange-membrane cells (a state-of-the-art technology) as a viable approach for conducting this reaction. This is expected to lead to more efficient and economical cell designs than were previously available. Considerable development and scale-up issues remain to be resolved, but the development of a viable commercial-scale HyS Process should be feasible in time to meet the commercialization schedule for Generation IV gas-cooled nuclear reactors.

Summers, William A.; Steimke, John L

2005-09-23T23:59:59.000Z

315

Thermochemical and kinetic aspects of the sulfurization of Cu-Sb and Cu-Bi thin films  

Science Conference Proceedings (OSTI)

CuSbS{sub 2} and Cu{sub 3}BiS{sub 3} are being investigated as part of a search for new absorber materials for photovoltaic devices. Thin films of these chalcogenides were produced by conversion of stacked and co-electroplated metal precursor layers in the presence of elemental sulfur vapour. Ex-situ XRD and SEM/EDS analyses of the processed samples were employed to study the reaction sequence with the aim of achieving compact layer morphologies. A new 'Time-Temperature-Reaction' (TTR) diagram and modified Pilling-Bedworth coefficients have been introduced for the description and interpretation of the reaction kinetics. For equal processing times, the minimum temperature required for CuSbS{sub 2} to appear is substantially lower than for Cu{sub 3}BiS{sub 3}, suggesting that interdiffusion across the interfaces between the binary sulfides is a key step in the formation of the ternary compounds. The effects of the heating rate and sulfur partial pressure on the phase evolution as well as the potential losses of Sb and Bi during the processes have been investigated experimentally and the results related to the equilibrium pressure diagrams obtained via thermochemical computation. - Graphical Abstract: Example of 3D plot showing the equilibrium pressure surfaces of species potentially escaping from chalcogenide films as a function of temperature and sulfur partial pressure. Bi{sub (g)}, Bi{sub 2(g)}, and BiS{sub (g)} are the gaseous species in equilibrium with solid Bi{sub 2}S{sub 3(s)} considered in this specific example. The pressure threshold plane corresponds to the pressure limit above which the elemental losses from 1 {mu}m thick films exceeds 10% of the original content per cm{sup 2} area of film and dm{sup 3} capacity of sulfurization furnace under static atmosphere conditions. The sulfurization temperature/sulfur partial pressure boundaries required to minimise the elemental losses below a given value can be easily read from the 2D projection of the intersection curves into the T-p{sub S2} plane. Highlights: Black-Right-Pointing-Triangle Sulfurization of Sb-Cu and Bi-Cu metal precursors for thin film PV applications. Black-Right-Pointing-Triangle Kinetics shows the rate determining step to be the interdiffusion of binary sulfides. Black-Right-Pointing-Triangle Phase evolution is consistent with Pilling-Bedworth coefficients of Cu, Sb and Bi. Black-Right-Pointing-Triangle Elemental losses can be minimised via the use of equilibrium pressure diagrams.

Colombara, Diego, E-mail: dc326@bath.ac.uk [Department of Chemistry, University of Bath, Bath BA2 7AY (United Kingdom); Peter, Laurence M. [Department of Chemistry, University of Bath, Bath BA2 7AY (United Kingdom); Rogers, Keith D.; Hutchings, Kyle [Centre for Materials Science and Engineering, Cranfield University, Shrivenham, SN6 8LA (United Kingdom)

2012-02-15T23:59:59.000Z

316

Badly Shaped Elements (BadlyShapedElements)  

Science Conference Proceedings (OSTI)

... shaped elements. Synopsis. BadlyShapedElements ( threshold ). Details. Base class: SkelModTargets; Parameters: threshold The threshold shape ...

2013-07-05T23:59:59.000Z

317

FUEL ELEMENT  

DOE Patents (OSTI)

A fuel element was developed for a gas cooled nuclear reactor. The element is constructed in the form of a compacted fuel slug including carbides of fissionable material in some cases with a breeder material carbide and a moderator which slug is disposed in a canning jacket of relatively impermeable moderator material. Such canned fuel slugs are disposed in an elongated shell of moderator having greater gas permeability than the canning material wherefore application of reduced pressure to the space therebetween causes gas diffusing through the exterior shell to sweep fission products from the system. Integral fission product traps and/or exterior traps as well as a fission product monitoring system may be employed therewith. (AEC)

Fortescue, P.; Zumwalt, L.R.

1961-11-28T23:59:59.000Z

318

Standard Elements  

Science Conference Proceedings (OSTI)

Table 1   ASTM standards applicable to element-level testing of composites...Composite Plates Subjected to a Distributed Load Plate flexure D 6484 Open-Hole Compression Strength of Polymer Matrix Composites Open-hole compression strength Z 5370Z Compression After Impact Strength of Fiber-Resin Composites Compression after impact Z 7225Z Mixed Mode I-Mode II...

319

Trace Metals in Oil Laboratory Proficiency Program  

Science Conference Proceedings (OSTI)

Lab Proficiency Testing service for Trace Metals in Oil. Soybean oil sample to test for Iron, Copper, and Nickel using AOCS Official method Ca 18-79. Trace Metals in Oil Laboratory Proficiency Program Laboratory Proficiency Program (LPP) aocs applicants

320

Environmental, health, and safety issues of sodium-sulfur batteries for electric and hybrid vehicles. Volume 3, Transport of sodium-sulfur and sodium-metal-chloride batteries  

DOE Green Energy (OSTI)

This report examines the shipping regulations that govern the shipment of dangerous goods. Since the elemental sodium contained in both sodium-sulfur and sodium-metal-chloride batteries is classified as a dangerous good, and is listed on both the national and international hazardous materials listings, both national and international regulatory processes are considered in this report The interrelationships as well as the differences between the two processes are highlighted. It is important to note that the transport regulatory processes examined in this report are reviewed within the context of assessing the necessary steps needed to provide for the domestic and international transport of sodium-beta batteries. The need for such an assessment was determined by the Shipping Sub-Working Group (SSWG) of the EV Battery Readiness Working Group (Working Group), created in 1990. The Working Group was created to examine the regulatory issues pertaining to in-vehicle safety, shipping, and recycling of sodium-sulfur batteries, each of which is addressed by a sub-working group. The mission of the SSWG is to establish basic provisions that will ensure the safe and efficient transport of sodium-beta batteries. To support that end, a proposal to the UN Committee of Experts was prepared by the SSWG, with the goal of obtaining a proper shipping name and UN number for sodium-beta batteries and to establish the basic transport requirements for such batteries (see the appendix for the proposal as submitted). It is emphasized that because batteries are large articles containing elemental sodium and, in some cases, sulfur, there is no existing UN entry under which they can be classified and for which modal transport requirements, such as the use of packaging appropriate for such large articles, are provided for. It is for this reason that a specific UN entry for sodium-beta batteries is considered essential.

Hammel, C.J.

1992-09-01T23:59:59.000Z

Note: This page contains sample records for the topic "trace elements 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

Process for production of synthesis gas with reduced sulfur content  

DOE Patents (OSTI)

A process for the partial oxidation of a sulfur- and silicate-containing carbonaceous fuel to produce a synthesis gas with reduced sulfur content which comprises partially oxidizing said fuel at a temperature in the range of 1800.degree.-2200.degree. F. in the presence of a temperature moderator, an oxygen-containing gas and a sulfur capture additive which comprises an iron-containing compound portion and a sodium-containing compound portion to produce a synthesis gas comprising H.sub.2 and CO with a reduced sulfur content and a molten slag which comprises (i) a sulfur-containing sodium-iron silicate phase and (ii) a sodium-iron sulfide phase. The sulfur capture additive may optionally comprise a copper-containing compound portion.

Najjar, Mitri S. (Hopewell Junction, NY); Corbeels, Roger J. (Wappingers Falls, NY); Kokturk, Uygur (Wappingers Falls, NY)

1989-01-01T23:59:59.000Z

322

Distributed trace using central performance counter memory  

SciTech Connect

A plurality of processing cores, are central storage unit having at least memory connected in a daisy chain manner, forming a daisy chain ring layout on an integrated chip. At least one of the plurality of processing cores places trace data on the daisy chain connection for transmitting the trace data to the central storage unit, and the central storage unit detects the trace data and stores the trace data in the memory co-located in with the central storage unit.

Satterfield, David L.; Sexton, James C.

2013-01-22T23:59:59.000Z

323

Distributed trace using central performance counter memory  

Science Conference Proceedings (OSTI)

A plurality of processing cores, are central storage unit having at least memory connected in a daisy chain manner, forming a daisy chain ring layout on an integrated chip. At least one of the plurality of processing cores places trace data on the daisy chain connection for transmitting the trace data to the central storage unit, and the central storage unit detects the trace data and stores the trace data in the memory co-located in with the central storage unit.

Satterfield, David L; Sexton, James C

2013-10-22T23:59:59.000Z

324

Removal of sulfur compounds from combustion product exhaust  

DOE Patents (OSTI)

A method and device are disclosed for removing sulfur containing contaminents from a combustion product exhaust. The removal process is carried out in two stages wherein the combustion product exhaust is dissolved in water, the water being then heated to drive off the sulfur containing contaminents. The sulfur containing gases are then resolublized in a cold water trap to form a concentrated solution which can then be used as a commercial product.

Cheng, Dah Y. (Palo Alto, CA)

1982-01-01T23:59:59.000Z

325

Abatement of Air Pollution: Control of Sulfur Compound Emissions  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Abatement of Air Pollution: Control of Sulfur Compound Emissions Abatement of Air Pollution: Control of Sulfur Compound Emissions (Connecticut) Abatement of Air Pollution: Control of Sulfur Compound Emissions (Connecticut) < Back Eligibility Agricultural Commercial Construction Fed. Government Fuel Distributor General Public/Consumer Industrial Installer/Contractor Institutional Investor-Owned Utility Local Government Low-Income Residential Multi-Family Residential Municipal/Public Utility Nonprofit Residential Retail Supplier Rural Electric Cooperative Schools State/Provincial Govt Systems Integrator Transportation Tribal Government Utility Program Info State Connecticut Program Type Environmental Regulations Provider Department of Energy and Environmental Protection These regulations set limits on the sulfur content of allowable fuels (1.0%

326

Mechanism of Sulfur-containing Aryl Polyphosphonate as Flame ...  

Science Conference Proceedings (OSTI)

Presentation Title, Mechanism of Sulfur-containing Aryl Polyphosphonate as Flame Retardant for PET. Author(s), Deng Yi. On-Site Speaker (Planned), Deng Yi.

327

Average prices for spot sulfur dioxide emissions allowances at ...  

U.S. Energy Information Administration (EIA)

The weighted average spot price for sulfur dioxide (SO 2) emissions allowances awarded to winning bidders at Environmental Protection Agency's (EPA) annual auction on ...

328

Polymer Electrolytes for Rechargeable Lithium/Sulfur Batteries.  

E-Print Network (OSTI)

??With the rapid development of portable electronics, hybrid-electric and electric cars, there is great interest in utilization of sulfur as cathodes for rechargeable lithium batteries. (more)

Zhao, Yan

2013-01-01T23:59:59.000Z

329

Better Batteries from Waste Sulfur - Materials Technology@TMS  

Science Conference Proceedings (OSTI)

Posted on: 04/28/2013. Transforming waste sulfur into lightweight plastic that could lead to better batteries for electric cars is possible through a new chemical

330

Reductive Sulfur-fixation Smelting of Stibnite Concentrate in Sodium ...  

Science Conference Proceedings (OSTI)

Abstract Scope, A new process to extracted antimony directly from stibnite concentrate by reductive sulfur-fixation smelting in sodium molten salt has been...

331

Low Temperature Sodium-Sulfur Grid Storage and EV Battery  

Berkeley Lab researcher Gao Liu has developed an innovative design for a battery, made primarily of sodium and sulfur, that holds promise for both ...

332

Available Technologies: Lithium / Sulfur Cells with Long Cycle ...  

A team of Berkeley Lab battery researchers led by Elton Cairns has invented an advanced lithium/sulfur (Li/S) cell that, for the first time, offers ...

333

Nanostructured Sulfur Electrodes for Long-Life Lithium Batteries  

Berkeley Lab researcher Elton Cairns has developed a technology that addresses limitations of developing a commercial-grade lithium / sulfur battery. ...

334

Low Temperature Sodium-Sulfur Grid Storage and EV Battery ...  

Berkeley Lab researcher Gao Liu has developed an innovative design for a battery, made primarily of sodium and sulfur, that holds promise for both large-scale grid ...

335

Conventional methods for removing sulfur and other contaminants...  

NLE Websites -- All DOE Office Websites (Extended Search)

Conventional methods for removing sulfur and other contaminants from syngas typically rely on chemical or physical absorption processes operating at low temperatures. When cooled...

336

Method of determining lanthanidies in a transition element host  

DOE Patents (OSTI)

A phosphor composition contains a lanthanide activator element within a host matrix having a transition element as a major component. The host matrix is composed of certain rare earth phosphates or vanadates such as YPO.sub.4 with a portion of the rare earth replaced with one or more of the transition elements. On X-ray or other electromagnetic excitation, trace lanthanide impurities or additives within the phosphor are spectrometrically determined from their characteristic luminescence.

De Kalb, Edward L. (Ames, IA); Fassel, Velmer A. (Ames, IA)

1976-02-03T23:59:59.000Z

337

Sulfur removal and comminution of carbonaceous material  

DOE Patents (OSTI)

Finely divided, clean coal or other carbonaceous material is provided by forming a slurry of coarse coal in aqueous alkali solution and heating the slurry under pressure to above the critical conditions of steam. The supercritical fluid penetrates and is trapped in the porosity of the coal as it swells in a thermoplastic condition at elevated temperature. By a sudden, explosive release of pressure the coal is fractured into finely divided particles with release of sulfur-containing gases and minerals. The finely divided coal is recovered from the minerals for use as a clean coal product.

Narain, Nand K. (Bethel Park, PA); Ruether, John A. (McMurray, PA); Smith, Dennis N. (Herminie, PA)

1988-01-01T23:59:59.000Z

338

Sulfur removal and comminution of carbonaceous material  

DOE Patents (OSTI)

Finely divided, clean coal or other carbonaceous material is provided by forming a slurry of coarse coal in aqueous alkali solution and heating the slurry under pressure to above the critical conditions of steam. The supercritical fluid penetrates and is trapped in the porosity of the coal as it swells in a thermoplastic condition at elevated temperature. By a sudden, explosive release of pressure the coal is fractured into finely divided particles with release of sulfur-containing gases and minerals. The finely divided coal is recovered from the minerals for use as a clean coal product. 2 figs.

Narain, N.K.; Ruether, J.A.; Smith, D.N.

1987-10-07T23:59:59.000Z

339

Sulfur, Chlorine, & Argon Abundances in Planetary Nebulae. I: Observations and Abundances in a Northern Sample  

E-Print Network (OSTI)

This paper is the first of a series specifically studying the abundances of sulfur, chlorine, and argon in Type II planetary nebulae (PNe) in the Galactic disk. Ratios of S/O, Cl/O, and Ar/O constitute important tests of differential nucleosynthesis of these elements and serve as strict constraints on massive star yield predictions. We present new ground-based optical spectra extending from 3600-9600 Angstroms for a sample of 19 Type II northern PNe. This range includes the strong near infrared lines of [S III] 9069,9532, which allows us to test extensively their effectiveness as sulfur abundance indicators. We also introduce a new, model-tested ionization correction factor for sulfur. For the present sample, we find average values of S/O=1.2E-2(+/- 0.71E-2), Cl/O=3.3E-4(+/- 1.6E-4), and Ar/O=5.0E-3(+/- 1.9E-3).

K. B. Kwitter; R. B. C. Henry

2001-06-12T23:59:59.000Z

340

MULTIPLE SULFUR ISOTOPE FRACTIONATIONS IN BIOLOGICAL SYSTEMS: A CASE STUDY WITH SULFATE REDUCERS  

E-Print Network (OSTI)

MULTIPLE SULFUR ISOTOPE FRACTIONATIONS IN BIOLOGICAL SYSTEMS: A CASE STUDY WITH SULFATE REDUCERS*, DONALD E. CANFIELD**, and KIRSTEN S. HABICHT** ABSTRACT. Multiple sulfur isotope measurements of sulfur disproportionation indicate that different types of metabolic processes impart differ- ent multiple isotope

Kaufman, Alan Jay

Note: This page contains sample records for the topic "trace elements 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

Plasma-chemical conversion of hydrogen sulfide into hydrogen and sulfur  

DOE Green Energy (OSTI)

A waste-treatment process that recovers both hydrogen and sulfur from hydrogen-sulfide-contaminated industrial wastes is being developed to replace the Claus technology, which recovers only sulfur. The proposed process is based on research reported in the Soviet technical literature and uses microwave (or radio-frequency) energy to initiate plasma-chemical reactions that dissociate hydrogen sulfide into elemental hydrogen and sulfur. In the plasma-chemical process, the gaseous stream would be purified and separated into streams containing the product hydrogen, hydrogen sulfide for recycle to the plasma reactor, and the process purge containing carbon dioxide and water. Since unconverted hydrogen sulfide is recycled to the plasma reactor, the plasma-chemical process has the potential for sulfur recoveries in excess of 99% without the additional tail-gas clean-up processes associated with the Claus technology. Laboratory experiments with pure hydrogen sulfide have confirmed that conversions of over 90% per pass are possible. Experiments with impurities typical of petroleum refinery and natural gas production acid gases have demonstrated that these impurities are compatible with the plasma dissociation process and do not appear to create new waste-treatment problems. Other experiments show that the cyclonic-flow pattern hypothesized by the Russian theoretical analysis of the plasma-chemical process can substantially decrease energy requirements for hydrogen sulfide dissociation while increasing conversion. This process has several advantages over the current Claus-plus-tail-gas-cleanup technology. The primary advantage is the potential for recovering hydrogen more cheaply than the direct production of hydrogen. The difference could amount to an energy savings of 40 {times} 10{sup 15} to 70 {times} 10{sup 15} J/yr in the refining industry, for an annual savings of $500 million to $1,000 million.

Harkness, J.B.L.; Doctor, R.D.; Daniels, E.J.

1993-09-01T23:59:59.000Z

342

It's Elemental - Isotopes of the Element Mendelevium  

NLE Websites -- All DOE Office Websites (Extended Search)

The Periodic Table of Elements Next Element (Nobelium) Nobelium Isotopes of the Element Mendelevium Click for Main Data Most of the isotope data on this site has been obtained...

343

It's Elemental - Isotopes of the Element Uranium  

NLE Websites -- All DOE Office Websites (Extended Search)

Periodic Table of Elements Next Element (Neptunium) Neptunium Isotopes of the Element Uranium Click for Main Data Most of the isotope data on this site has been obtained from...

344

It's Elemental - Isotopes of the Element Lithium  

NLE Websites -- All DOE Office Websites (Extended Search)

Periodic Table of Elements Next Element (Beryllium) Beryllium Isotopes of the Element Lithium Click for Main Data Most of the isotope data on this site has been obtained from...

345

It's Elemental - Isotopes of the Element Hydrogen  

NLE Websites -- All DOE Office Websites (Extended Search)

The Periodic Table of Elements Next Element (Helium) Helium Isotopes of the Element Hydrogen Click for Main Data Most of the isotope data on this site has been obtained from...

346

Integrated boiler, superheater, and decomposer for sulfuric acid decomposition  

DOE Patents (OSTI)

A method and apparatus, constructed of ceramics and other corrosion resistant materials, for decomposing sulfuric acid into sulfur dioxide, oxygen and water using an integrated boiler, superheater, and decomposer unit comprising a bayonet-type, dual-tube, counter-flow heat exchanger with a catalytic insert and a central baffle to increase recuperation efficiency.

Moore, Robert (Edgewood, NM); Pickard, Paul S. (Albuquerque, NM); Parma, Jr., Edward J. (Albuquerque, NM); Vernon, Milton E. (Albuquerque, NM); Gelbard, Fred (Albuquerque, NM); Lenard, Roger X. (Edgewood, NM)

2010-01-12T23:59:59.000Z

347

Process for removing pyritic sulfur from bituminous coals  

DOE Patents (OSTI)

A process is provided for removing pyritic sulfur and lowering ash content of bituminous coals by grinding the feed coal, subjecting it to micro-agglomeration with a bridging liquid containing heavy oil, separating the microagglomerates and separating them to a water wash to remove suspended pyritic sulfur. In one embodiment the coal is subjected to a second micro-agglomeration step.

Pawlak, Wanda (Edmonton, CA); Janiak, Jerzy S. (Edmonton, CA); Turak, Ali A. (Edmonton, CA); Ignasiak, Boleslaw L. (Edmonton, CA)

1990-01-01T23:59:59.000Z

348

Sodium sulfur container with chromium/chromium oxide coating  

SciTech Connect

A coating of chromium/chromium oxide is disclosed for coating the surfaces of electrically conducting components of a sodium sulfur battery. This chromium/chromium oxide coating is placed on the surfaces of the electrically conducting components of the battery which are in contact with molten polysulfide and sulfur reactants during battery operation.

Ludwig, Frank A. (Irvine, CA); Higley, Lin R. (Santa Ana, CA)

1981-01-01T23:59:59.000Z

349

Historical Sulfur Dioxide Emissions 1850-2000: Methods and Results  

E-Print Network (OSTI)

PNNL-14537 Historical Sulfur Dioxide Emissions 1850-2000: Methods and Results S.J. Smith E;PNNL-14537 Historical Sulfur Dioxide Emissions 1850-2000: Methods and Results PNNL Research Report Joint Global Change Research Institute 8400 Baltimore Avenue College Park, Maryland 20740 #12;PNNL-14537

Hultman, Nathan E.

350

High-sulfur coals in the eastern Kentucky coal field  

Science Conference Proceedings (OSTI)

The Eastern Kentucky coal field is notable for relatively low-sulfur, [open quotes]compliance[close quotes] coals. Virtually all of the major coals in this area do have regions in which higher sulfur lithotypes are common, if not dominant, within the lithologic profile. Three Middle Pennsylvanian coals, each representing a major resource, exemplify this. The Clintwood coal bed is the stratigraphically lowest coal bed mined throughout the coal field. In Whitley County, the sulfur content increase from 0.6% at the base to nearly 12% in the top lithotype. Pyrite in the high-sulfur lithotype is a complex mixture of sub- to few-micron syngenetic forms and massive epigenetic growths. The stratigraphically higher Pond Creek coal bed is extensively mined in portions of the coal field. Although generally low in sulfur, in northern Pike and southern Martin counties the top one-third can have up to 6% sulfur. Uniformly low-sulfur profiles can occur within a few hundred meters of high-sulfur coal. Pyrite occurs as 10-50 [mu]m euhedra and coarser massive forms. In this case, sulfur distribution may have been controlled by sandstone channels in the overlying sediments. High-sulfur zones in the lower bench of the Fire Clay coal bed, the stratigraphically highest coal bed considered here, are more problematical. The lower bench, which is of highly variable thickness and quality, generally is overlain by a kaolinitic flint clay, the consequence of a volcanic ash fall into the peat swamp. In southern Perry and Letcher counties, a black, illite-chlorite clay directly overlies the lower bench. General lack of lateral continuity of lithotypes in the lower bench suggests that the precursor swamp consisted of discontinuous peat-forming environments that were spatially variable and regularly inundated by sediments. Some of the peat-forming areas may have been marshlike in character.

Hower, J.C.; Graham, U.M. (Univ. of Kentucky Center for Applied Energy Research, Lexington, KY (United States)); Eble, C.F. (Kentucky Geological Survey, Lexington, KY (United States))

1993-08-01T23:59:59.000Z

351

Bench-scale testing and evaluation of the direct sulfur recovery process. Final report, February 1990--March 1994  

SciTech Connect

The Direct Sulfur Recovery Process (DSRP) is a two-stage catalytic reduction process for efficiently recovering up to 99% or higher amounts of elemental sulfur from SO{sub 2}-containing regeneration tail-gas produced in advanced integrated gasification combined cycle (IGCC) power systems by reacting the tail-gas with a small slipstream of coal gas. In this project, the DSRP was demonstrated with simulated gases at bench-scale with 3-in. diameter, 1-L size catalytic reactors. Fundamental kinetic and modeling studies were conducted to explain the significantly higher than thermodynamically expected sulfur recoveries in DSRP and to enable prediction of sulfur recovery in larger reactors. Technology transfer activities to promote the DSRP consisted of publications and discussions with architectural engineering firms and industrial parties especially IGCC system developers. Toward the end of the project, an agreement was signed with an IGCC system developer to scale up the DSRP and test it with actual gases in their 10-MW (thermal) coal gasification pilot-plant under a cooperative R&D agreement with the US Department of Energy.

Gangwal, S.K.; Chen, D.H.

1994-05-01T23:59:59.000Z

352

CX-001459: Categorical Exclusion Determination | Department of...  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Determination Air Quality VIII: An International Conference on Carbon Management, Mercury, Trace Elements, Sulfur Oxide (SOx), Nitrogen Oxide (NOx) CX(s) Applied: A9 Date: 03...

353

International Best Practices for Pre-Processing and Co-Processing Municipal Solid Waste and Sewage Sludge in the Cement Industry  

E-Print Network (OSTI)

dioxins and furans, HCl, chlorine gas, Pb, manganese, andas calorific value and chlorine, ash, and trace element (influence setting time Chlorine, sulfur, and alkali, which

Hasanbeigi, Ali

2013-01-01T23:59:59.000Z

354

Environmental, health, and safety issues of sodium-sulfur batteries for electric and hybrid vehicles  

DOE Green Energy (OSTI)

This report examines the shipping regulations that govern the shipment of dangerous goods. Since the elemental sodium contained in both sodium-sulfur and sodium-metal-chloride batteries is classified as a dangerous good, and is listed on both the national and international hazardous materials listings, both national and international regulatory processes are considered in this report The interrelationships as well as the differences between the two processes are highlighted. It is important to note that the transport regulatory processes examined in this report are reviewed within the context of assessing the necessary steps needed to provide for the domestic and international transport of sodium-beta batteries. The need for such an assessment was determined by the Shipping Sub-Working Group (SSWG) of the EV Battery Readiness Working Group (Working Group), created in 1990. The Working Group was created to examine the regulatory issues pertaining to in-vehicle safety, shipping, and recycling of sodium-sulfur batteries, each of which is addressed by a sub-working group. The mission of the SSWG is to establish basic provisions that will ensure the safe and efficient transport of sodium-beta batteries. To support that end, a proposal to the UN Committee of Experts was prepared by the SSWG, with the goal of obtaining a proper shipping name and UN number for sodium-beta batteries and to establish the basic transport requirements for such batteries (see the appendix for the proposal as submitted). It is emphasized that because batteries are large articles containing elemental sodium and, in some cases, sulfur, there is no existing UN entry under which they can be classified and for which modal transport requirements, such as the use of packaging appropriate for such large articles, are provided for. It is for this reason that a specific UN entry for sodium-beta batteries is considered essential.

Hammel, C.J.

1992-09-01T23:59:59.000Z

355

Linear driving force models for dynamic adsorption of volatile organic compound traces by porous adsorbent beds  

Science Conference Proceedings (OSTI)

Models for the dynamic adsorption of volatile organic compound (VOC) traces in air are considered. They are based on the linear driving force approximation associated with various adsorption isotherms characteristic of the couple VOC-adsorbent (Langmuir, ... Keywords: Comsol, Dubinin-Astakhov isotherm, Dynamic adsorption modelling, Finite element

Agns Joly; Alain Perrard

2009-08-01T23:59:59.000Z

356

Performance and cost models for the direct sulfur recovery process. Task 1 Topical report, Volume 3  

SciTech Connect

The purpose of this project is to develop performance and cost models of the Direct Sulfur Recovery Process (DSRP). The DSRP is an emerging technology for sulfur recovery from advanced power generation technologies such as Integrated Gasification Combined Cycle (IGCC) systems. In IGCC systems, sulfur present in the coal is captured by gas cleanup technologies to avoid creating emissions of sulfur dioxide to the atmosphere. The sulfur that is separated from the coal gas stream must be collected. Leading options for dealing with the sulfur include byproduct recovery as either sulfur or sulfuric acid. Sulfur is a preferred byproduct, because it is easier to handle and therefore does not depend as strongly upon the location of potential customers as is the case for sulfuric acid. This report describes the need for new sulfur recovery technologies.

Frey, H.C. [North Carolina State Univ., Raleigh, NC (United States); Williams, R.B. [Carneigie Mellon Univ., Pittsburgh, PA (United States)

1995-09-01T23:59:59.000Z

357

Trace gases could double climate warming  

SciTech Connect

The atmospheric concentrations of several trace gases capable of changing the climate are increasing. Researchers are concerned about the trace gases despite their miniscule concentrations because they are such efficient absorbers of far-infrared radiation. The trace gases that concern climatologists are methane, nitrous oxide, and the chlorofluorocarbons or CFC's. The increase in atmospheric concentrations of these gases are discussed and atmospheric models predicting their greenhouse effect are described.

Kerr, R.A.

1983-06-24T23:59:59.000Z

358

Oxidation of elemental mercury by chlorine: Gas phase, Surface, and Photo-induced reaction pathways  

E-Print Network (OSTI)

of Air Quality III: Mercury, Trace Elements, and Particulate34, 2711. 7. Sloss, L.L. Mercury Emissions and Control.1996 , Jan. , 60 pp. 2. Mercury Study Report to Congress;

Yan, Nai-Qiang; Liu, Shou-Heng; Chang, Shih-Ger

2004-01-01T23:59:59.000Z

359

Visualization and observations on traces - CECM  

E-Print Network (OSTI)

Nov 19, 1997 ... A similar quality appears in resulting columns of a 2-trace operation with the difference that the pattern now merges aspects of the truth table...

360

Terpolymerization of ethylene, sulfur dioxide and carbon monoxide  

DOE Patents (OSTI)

This invention relates to a high molecular weight terpolymer of ethylene, sulfur dioxide and carbon monoxide stable to 280.degree. C. and containing as little as 36 mol % ethylene and about 41-51 mol % sulfur dioxide; and to the method of producing said terpolymer by irradiation of a liquid and gaseous mixture of ethylene, sulfur dioxide and carbon monoxide by means of Co-60 gamma rays or an electron beam, at a temperature of about 10.degree.-50.degree. C., and at a pressure of about 140 to 680 atmospheres, to initiate polymerization.

Johnson, Richard (Shirley, NY); Steinberg, Meyer (Huntington Station, NY)

1981-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "trace elements 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

Measurement of Trace Uranium Isotopes  

Science Conference Proceedings (OSTI)

The extent to which thermal ionization mass spectrometry (TIMS) can measure trace quantities of 233U and 236U in the presence of a huge excess of natural uranium is evaluated. This is an important nuclear non-proliferation measurement. Four ion production methods were evaluated with three mass spectrometer combinations. The most favorable combinations are not limited by abundance sensitivity; rather, the limitations are the ability to generate a uranium ion beam of sufficient intensity to obtain the required number of counts on the minor isotopes in relationship to detector background. The most favorable situations can measure isotope ratios in the range of E10 if sufficient sample intensity is available. These are the triple sector mass spectrometer with porous ion emitters (PIE) and the single sector mass spectrometer with energy filtering.

Matthew G. Watrous; James E. Delmore

2011-05-01T23:59:59.000Z

362

Low Temperature Sorbents for removal of Sulfur Compounds from fluid feed Streams  

DOE Patents (OSTI)

A sorbent material is provided comprising a material reactive with sulfur, a binder unreactive with sulfur and an inert material, wherein the sorbent absorbs the sulfur at temperatures between 30 and 200 C. Sulfur absorption capacity as high as 22 weight percent has been observed with these materials.

Siriwardane, Ranjan

1999-09-30T23:59:59.000Z

363

Low Temperature Sorbents for Removal of Sulfur Compounds from Fluid Feed Streams  

DOE Patents (OSTI)

A sorbent material is provided comprising a material reactive with sulfur, a binder unreactive with sulfur and an inert material, wherein the sorbent absorbs the sulfur at temperatures between 30 and 200 C. Sulfur absorption capacity as high as 22 weight percent has been observed with these materials.

Siriwardane, Ranjani

2004-06-01T23:59:59.000Z

364

Diagnostic tracing for wireless sensor networks  

Science Conference Proceedings (OSTI)

Wireless sensor networks are typically deployed in harsh environments, thus post-deployment failures are not infrequent. An execution trace containing events in their order of execution could play a crucial role in postmortem diagnosis of these failures. ... Keywords: Embedded debugging, diagnosis, tracing, wireless sensor networks

Vinaitheerthan Sundaram; Patrick Eugster; Xiangyu Zhang; Vamsidhar Addanki

2013-07-01T23:59:59.000Z

365

System for adding sulfur to a fuel cell stack system for improved fuel cell stability  

DOE Patents (OSTI)

A system for adding sulfur to a reformate stream feeding a fuel cell stack, having a sulfur source for providing sulfur to the reformate stream and a metering device in fluid connection with the sulfur source and the reformate stream. The metering device injects sulfur from the sulfur source to the reformate stream at a predetermined rate, thereby providing a conditioned reformate stream to the fuel cell stack. The system provides a conditioned reformate stream having a predetermined sulfur concentration that gives an acceptable balance of minimal drop in initial power with the desired maximum stability of operation over prolonged periods for the fuel cell stack.

Mukerjee, Subhasish; Haltiner, Jr., Karl J; Weissman, Jeffrey G

2013-08-13T23:59:59.000Z

366

Martinez Sulfuric Acid Regeneration Plt Biomass Facility | Open Energy  

Open Energy Info (EERE)

Martinez Sulfuric Acid Regeneration Plt Biomass Facility Martinez Sulfuric Acid Regeneration Plt Biomass Facility Jump to: navigation, search Name Martinez Sulfuric Acid Regeneration Plt Biomass Facility Facility Martinez Sulfuric Acid Regeneration Plt Sector Biomass Facility Type Non-Fossil Waste Location Contra Costa County, California Coordinates 37.8534093°, -121.9017954° 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":37.8534093,"lon":-121.9017954,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

367

Diesel Emissions Control-Sulfur Effects (DECSE) Program Status  

DOE Green Energy (OSTI)

Determine the impact of fuel sulfur levels on emission control systems that could be implemented to lower emissions of NO{sub x} and PM from on-highway trucks in the 2002-2004 time frame.

None

1999-06-29T23:59:59.000Z

368

Novel Sulfur-Tolerant Anodes for Solid Oxide Fuel Cells  

DOE Green Energy (OSTI)

One of the unique advantages of SOFCs over other types of fuel cells is the potential for direct utilization of hydrocarbon fuels (it may involve internal reforming). Unfortunately, most hydrocarbon fuels contain sulfur, which would dramatically degrade SOFC performance at parts-per-million (ppm) levels. Low concentration of sulfur (ppm or below) is difficult to remove efficiently and cost-effectively. Therefore, knowing the exact poisoning process for state-of-the-art anode-supported SOFCs with Ni-YSZ cermet anodes, understanding the detailed anode poisoning mechanism, and developing new sulfur-tolerant anodes are essential to the promotion of SOFCs that run on hydrocarbon fuels. The effect of cell operating conditions (including temperature, H{sub 2}S concentration, cell voltage/current density, etc.) on sulfur poisoning and recovery of nickel-based anode in SOFCs was investigated. It was found that sulfur poisoning is more severe at lower temperature, higher H{sub 2}S concentration or lower cell current density (higher cell voltage). In-situ Raman spectroscopy identified the nickel sulfide formation process on the surface of a Ni-YSZ electrode and the corresponding morphology change as the sample was cooled in H{sub 2}S-containing fuel. Quantum chemical calculations predicted a new S-Ni phase diagram with a region of sulfur adsorption on Ni surfaces, corresponding to sulfur poisoning of Ni-YSZ anodes under typical SOFC operating conditions. Further, quantum chemical calculations were used to predict the adsorption energy and bond length for sulfur and hydrogen atoms on various metal surfaces. Surface modification of Ni-YSZ anode by thin Nb{sub 2}O{sub 5} coating was utilized to enhance the sulfur tolerance. A multi-cell testing system was designed and constructed which is capable of simultaneously performing electrochemical tests of 12 button cells in fuels with four different concentrations of H{sub 2}S. Through systematical study of state-of-the-art anode-supported SOFC button cells, it is seen that the long-term sulfur poisoning behavior of those cells indicate that there might be a second-stage slower degradation due to sulfur poisoning, which would last for a thousand hour or even longer. However, when using G-18 sealant from PNNL, the 2nd stage poisoning was effectively prohibited.

Lei Yang; Meilin Liu

2008-12-31T23:59:59.000Z

369

METHOD TO PREVENT SULFUR ACCUMULATION INSIDE MEMBRANE ELECTRODE ASSEMBLY  

DOE Green Energy (OSTI)

HyS is conceptually the simplest of the thermochemical cycles and involves only sulfur chemistry. In the HyS Cycle hydrogen gas (H{sub 2}) is produced at the cathode of the electrochemical cell (or electrolyzer). Sulfur dioxide (SO{sub 2}) is oxidized at the anode to form sulfuric acid (H{sub 2}SO{sub 4}) and protons (H{sup +}) as illustrated below. A separate high temperature reaction decomposes the sulfuric acid to water and sulfur dioxide which are recycled to the electrolyzers, and oxygen which is separated out as a secondary product. The electrolyzer includes a membrane that will allow hydrogen ions to pass through but block the flow of hydrogen gas. The membrane is also intended to prevent other chemical species from migrating between electrodes and undergoing undesired reactions that could poison the cathode or reduce overall process efficiency. In conventional water electrolysis, water is oxidized at the anode to produce protons and oxygen. The standard cell potential for conventional water electrolysis is 1.23 volts at 25 C. However, commercial electrolyzers typically require higher voltages ranging from 1.8 V to 2.6 V [Kirk-Othmer, 1991]. The oxidation of sulfur dioxide instead of water in the HyS electrolyzer occurs at a much lower potential. For example, the standard cell potential for sulfur dioxide oxidation at 25 C in 50 wt % sulfuric acid is 0.29 V [Westinghouse, 1980]. Since power consumption by the electrolyzers is equal to voltage times current, and current is proportional to hydrogen production, a large reduction in voltage results in a large reduction in electrical power cost per unit of hydrogen generated.

Steimke, J.; Steeper, T.; Herman, D.; Colon-Mercado, H.; Elvington, M.

2009-06-22T23:59:59.000Z

370

THE RAVE CATALOG OF STELLAR ELEMENTAL ABUNDANCES: FIRST DATA RELEASE  

Science Conference Proceedings (OSTI)

We present chemical elemental abundances for 36,561 stars observed by the RAdial Velocity Experiment (RAVE), an ambitious spectroscopic survey of our Galaxy at Galactic latitudes |b| > 25 Degree-Sign and with magnitudes in the range 9 pipeline in which the curve of growth of individual lines is obtained from a library of absorption line equivalent widths to construct a model spectrum that is then matched to the observed spectrum via a {chi}{sup 2} minimization technique. We plan to extend this pipeline to include estimates for other elements, such as oxygen and sulfur, in future data releases.

Boeche, C.; Williams, M.; De Jong, R. S.; Steinmetz, M. [Leibniz-Institut fuer Astrophysik Potsdam (AIP), D-14482 Potsdam (Germany); Siebert, A.; Bienayme, O. [Observatoire Astronomique de Strasbourg, Universite de Strasbourg, CNRS, UMR 7550, F-67000 Strasbourg (France); Fulbright, J. P.; Ruchti, G. R. [Department of Physics and Astronomy, Johns Hopkins University, Baltimore, MD 21218 (United States); Bland-Hawthorn, J. [Sydney Institute for Astronomy, School of Physics A28, University of Sydney, NSW 2006 (Australia); Campbell, R. [Department of Physics and Astronomy, Western Kentucky University, Bowling Green, KY (United States); Freeman, K. C. [Research School of Astronomy and Astrophysics, Australia National University, Weston Creek, Canberra ACT 2611 (Australia); Gibson, B. K. [Jeremiah Horrocks Institute, University of Central Lancashire, Preston PR1 2HE (United Kingdom); Gilmore, G. [Institute of Astronomy, University of Cambridge, Madingley Road, Cambridge CB3 0HA (United Kingdom); Grebel, E. K. [Astronomisches Rechen-Institut, Zentrum fuer Astronomie der Universitaet Heidelberg, D-69120 Heidelberg (Germany); Helmi, A. [Kapteyn Astronomical Institute, University of Groningen, 9700 AV Groningen (Netherlands); Munari, U. [INAF Osservatorio Astronomico di Padova, Asiago I-36012 (Italy); Navarro, J. F. [Department of Physics and Astronomy, University of Victoria, Victoria BC V8W 3P6 (Canada); Parker, Q. A.; Reid, W. [Department of Physics and Astronomy, Faculty of Sciences, Macquarie University, Sydney, NSW 2109 (Australia); Seabroke, G. M. [Mullard Space Science Laboratory, University College London, Holmbury, St. Mary RH5 6NT (United Kingdom); and others

2011-12-15T23:59:59.000Z

371

Analysis for sulfur forms in coal and on coal surfaces  

SciTech Connect

A review and critical evaluation of all available literature on the determination of sulfur and sulfur forms in coal and on coal and pyrite surfaces is being performed. Approximately 200 citations through 1984 have been catalogued and reviewed, and approximately 100 additional citations since 1984 have been identified. Work is nearing completion on the collection and critical evaluation of the more recent literature. A few articles requested through the interlibrary loan system still need to be received and analyzed, and several articles in unusual foreign languages need to be evaluated. Methods used for sampling, sample preparation, and analysis of sulfur and sulfur forms in samples arising from the spherical oil agglomeration process have been reviewed. Recommendations are being made for assessing the quality of analyses provided by commercial laboratories, for assuring that preparation procedures do not alter sulfur forms in samples, and for determining the ability of sampling procedures to obtain representative samples. Several concerns about the applicability of the ASTM procedure for the determination of pyrite sulfur in micronized coal and oil-agglomerated samples have been raised. 5 refs., 1 tab.

Markuszewski, R.; Chriswell, C.D.; Norton, G.A.

1988-12-01T23:59:59.000Z

372

Advances in Acid Concentration Membrane Technology for the Sulfur-Iodine Thermochemical Cycle  

DOE Green Energy (OSTI)

One of the most promising cycles for the thermochemical generation of hydrogen is the Sulfur-Iodine (S-I) process, where aqueous HI is thermochemically decomposed into H2 and I2 at approximately 350 degrees Celsius. Regeneration of HI is accomplished by the Bunsen reaction (reaction of SO2, water, and iodine to generate H2SO4 and HI). Furthermore, SO2 is regenerated from the decomposition of H2SO4 at 850 degrees Celsius yielding the SO2 as well as O2. Thus, the cycle actually consists of two concurrent oxidation-reduction loops. As HI is regenerated, co-produced H2SO4 must be separated so that each may be decomposed. Current flowsheets employ a large amount (~83 mol% of the entire mixture) of elemental I2 to cause the HI and the H2SO4 to separate into two phases. To aid in the isolation of HI, which is directly decomposed into hydrogen, water and iodine must be removed. Separation of iodine is facilitated by removal of water. Sulfuric acid concentration is also required to facilitate feed recycling to the sulfuric acid decomposer. Decomposition of the sulfuric acid is an equilibrium limited process that leaves a substantial portion of the acid requiring recycle. Distillation of water from sulfuric acid involves significant corrosion issues at the liquid-vapor interface. Thus, it is desirable to concentrate the acid without boiling. Recent efforts at the INL have concentrated on applying pervaporation through Nafion-117, Nafion-112, and sulfonated poly(etheretherketone) (S-PEEK) membranes for the removal of water from HI/water and HI/Iodine/water feedstreams. In pervaporation, a feed is circulated at low pressure across the upstream side of the membrane, while a vacuum is applied downstream. Selected permeants sorb into the membrane, transport through it, and are vaporized from the backside. Thus, a concentration gradient is established, which provides the driving force for transport. In this work, membrane separations have been performed at temperatures as high as 134 degrees Celsius. Transmembrane fluxes of water are commercially competitive (~5000 g/m2h) and separation factors have been measured as high as 8000, depending on the membrane and the water content. For the Nafion-117 experiments, the common trade off in membrane performance is observed in that as flux is increased, separation factor decreases. Nafion-112, a thinner membrane, exhibited much higher fluxes than the Nafion-117; however without the expected loss in separation factor indicating that the permeability of iodine and HI through Nafion materials is low. Preliminary data for the sulfuric acid concentration suggests performance similar to the HI experiments. All membranes studied for the HI, HI/iodine and sulfuric acid feeds exhibited no degradation in membrane performance during use.

Frederick F. Stewart; Christopher J. Orme

2006-11-01T23:59:59.000Z

373

COMPONENT DEVELOPMENT NEEDS FOR THE HYBRID SULFUR ELECTROLYZER  

DOE Green Energy (OSTI)

Fiscal year 2008 studies in electrolyzer component development have focused on the characterization of membrane electrode assemblies (MEA) after performance tests in the single cell electrolyzer, evaluation of electrocatalysts and membranes using a small scale electrolyzer and evaluating the contribution of individual cell components to the overall electrochemical performance. Scanning electron microscopic (SEM) studies of samples taken from MEAs testing in the SRNL single cell electrolyzer test station indicates a sulfur-rich layer forms between the cathode catalyst layer and the membrane. Based on a review of operating conditions for each of the MEAs evaluated, we conclude that the formation of the layer results from the reduction of sulfur dioxide as it passes through the MEA and reaches the catalyst layer at the cathode-membrane interface. Formation of the sulfur rich layer results in partial delamination of the cathode catalyst layer leading to diminished performance. Furthermore we believe that operating the electrolyzer at elevated pressure significantly increases the rate of formation due to increased adsorption of hydrogen on the internal catalyst surface. Thus, identification of a membrane that exhibits much lower transport of sulfur dioxide is needed to reduce the quantity of sulfur dioxide that reaches the cathode catalyst and is reduced to produce the sulfur-rich layer. Three candidate membranes are currently being evaluated that have shown promise from preliminary studies, (1) modified Nafion{reg_sign}, (2) polybenzimidazole (PBI), and (3) sulfonated Diels Alder polyphenylene (SDAPP). Testing examined the activity for the sulfur dioxide oxidation of platinum (Pt) and platinum-alloy catalysts in 30 wt% sulfuric acid solution. Linear sweep voltammetry showed an increase in activity when catalysts in which Pt is alloyed with non-noble transition metals such as cobalt and chromium. However when Pt is alloyed with noble metals, such as iridium or ruthenium, the kinetic activity decreases. We recommend further testing to determine if these binary alloys will provide the increased reaction kinetic needed to meet the targets. We also plan to test the performance of these catalyst materials for both proton and sulfur dioxide reduction. The latter may provide another parameter by which we can control the reduction of sulfur dioxide upon transport to the cathode catalyst surface. A small scale electrolyzer (2 cm{sup 2}) has been fabricated and successfully installed as an additional tool to evaluate the effect of different operating conditions on electrolyzer and MEA performance. Currently this electrolyzer is limited to testing at temperatures up to 80 C and at atmospheric pressure. Selected electrochemical performance data from the single cell sulfur dioxide depolarized electrolyzer were analyzed with the aid of an empirical equation which takes into account the overpotential of each of the components. By using the empirical equation, the performance data was broken down into its components and a comparison of the potential losses was made. The results indicated that for the testing conditions of 80 C and 30 wt% sulfuric acid, the major overpotential contribution ({approx}70 % of all losses) arise from the slow reaction rate of oxidation of sulfur dioxide. The results indicate that in order to meet the target of hydrogen production at 0.5 A/cm{sup 2} at 0.6 V and 50 wt% sulfuric acid, identification of a better catalyst for sulfur dioxide oxidation will provide the largest gain in electrolyzer performance.

Hobbs, D; Hector Colon-Mercado, H; Mark Elvington, M

2008-05-30T23:59:59.000Z

374

TBBT: scalable and accurate trace replay for file server evaluation  

Science Conference Proceedings (OSTI)

This paper describes the design, implementation, and evaluation of TBBT, the first comprehensive NFS trace replay tool. Given an NFS trace, TBBT automatically detects and repairs missing operations in the trace, derives a file system image required to ...

Ningning Zhu; Jiawu Chen; Tzi-Cker Chiueh

2005-12-01T23:59:59.000Z

375

Easy system call tracing for Plan 9.  

SciTech Connect

Tracing system calls makes debugging easy and fast. On Plan 9, traditionally, system call tracing has been implemented with acid. New systems do not always implement all the capabilities needed for Acid, particularly the ability to rewrite the process code space to insert breakpoints. Architecture support libraries are not always available for Acid, or may not work even on a supported architecture. The requirement that Acid's libraries be available can be a problem on systems with a very small memory footprint, such as High Performance Computing systems where every Kbyte counts. Finally, Acid tracing is inconvenient in the presence of forks, which means tracing shell pipelines is particularly troublesome. The strace program available on most Unix systems is far more convenient to use and more capable than Acid for system call tracing. A similar system on Plan 9 can simplify troubleshooting. We have built a system calling tracing capability into the Plan 9 kernel. It has proven to be more convenient than strace in programming effort. One can write a shell script to implement tracing, and the C code to implement an strace equivalent is several orders of magnitude smaller.

Minnich, Ronald G.

2010-09-01T23:59:59.000Z

376

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

E-Print Network (OSTI)

Shi, J.B. ; Feng, X.B. Mercury Pollution in China. Environ.J T. DOE/NETLs Phase II Mercury Control Technology Fieldoxidants for the oxidation of mercury gas. Ind. vEng. Chem.

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

2008-01-01T23:59:59.000Z

377

Vapor Phase Elemental Sulfur Tech Brief DRAFT bbl 08-24  

saturated heated gas into access wells to distribute the gas throughout the site. Solid ... need to inject liquid/fluids). ...

378

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

E-Print Network (OSTI)

of Catalysts for Oxidation of Mercury in Flue Gas, Environ.mercury oxidation when the chlorine concentration in flue gas

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

2008-01-01T23:59:59.000Z

379

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

E-Print Network (OSTI)

removal from flue gas of coal-fired power plants. Environ.Speciation in a 100-MW Coal-Fired Boiler with Low-NOxControl Technologies for Coal-Fired Power Plants, DOE/NETL

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

2008-01-01T23:59:59.000Z

380

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

E-Print Network (OSTI)

from flue gas of coal-fired power plants. Environ. Sci. &Technologies for Coal-Fired Power Plants, DOE/NETL Mercurynumber of coal-fired generating plants (1-3). The mercury is

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

2008-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "trace elements 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

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

SciTech Connect

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

382

Lithium-Sulfur Batteries: Development of High Energy Lithium-Sulfur Cells for Electric Vehicle Applications  

SciTech Connect

BEEST Project: Sion Power is developing a lithium-sulfur (Li-S) battery, a potentially cost-effective alternative to the Li-Ion battery that could store 400% more energy per pound. All batteries have 3 key partsa positive and negative electrode and an electrolytethat exchange ions to store and release electricity. Using different materials for these components changes a batterys chemistry and its ability to power a vehicle. Traditional Li-S batteries experience adverse reactions between the electrolyte and lithium-based negative electrode that ultimately limit the battery to less than 50 charge cycles. Sion Power will sandwich the lithium- and sulfur-based electrode films around a separator that protects the negative electrode and increases the number of charges the battery can complete in its lifetime. The design could eventually allow for a battery with 400% greater storage capacity per pound than Li-Ion batteries and the ability to complete more than 500 recharge cycles.

2010-10-01T23:59:59.000Z

383

Hybrid Sulfur Thermochemical Process Development Annual Report  

DOE Green Energy (OSTI)

The Hybrid Sulfur (HyS) Thermochemical Process is a means of producing hydrogen via water-splitting through a combination of chemical reactions and electrochemistry. Energy is supplied to the system as high temperature heat (approximately 900 C) and electricity. Advanced nuclear reactors (Generation IV) or central solar receivers can be the source of the primary energy. Large-scale hydrogen production based on this process could be a major contributor to meeting the needs of a hydrogen economy. This project's objectives include optimization of the HyS process design, analysis of technical issues and concerns, creation of a development plan, and laboratory-scale proof-of-concept testing. The key component of the HyS Process is the SO2-depolarized electrolyzer (SDE). Studies were performed that showed that an electrolyzer operating in the range of 500-600 mV per cell can lead to an overall HyS cycle efficiency in excess of 50%, which is superior to all other currently proposed thermochemical cycles. Economic analysis indicated hydrogen production costs of approximately $1.60 per kilogram for a mature nuclear hydrogen production plant. However, in order to meet commercialization goals, the electrolyzer should be capable of operating at high current density, have a long operating lifetime , and have an acceptable capital cost. The use of proton-exchange-membrane (PEM) technology, which leverages work for the development of PEM fuel cells, was selected as the most promising route to meeting these goals. The major accomplishments of this project were the design and construction of a suitable electrolyzer test facility and the proof-of-concept testing of a PEM-based SDE.

Summers, William A.; Buckner, Melvin R.

2005-07-21T23:59:59.000Z

384

TRACING FLUID SOURCES IN THE COSO GEOTHERMAL SYSTEM USING FLUID...  

Open Energy Info (EERE)

TRACING FLUID SOURCES IN THE COSO GEOTHERMAL SYSTEM USING FLUID-INCLUSION GAS CHEMISTRY Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Conference Proceedings: TRACING...

385

Microwave Plasma Monitoring System For Real-Time Elemental Analysis  

NLE Websites -- All DOE Office Websites (Extended Search)

Microwave Plasma Monitoring System For Real-Time Elemental Analysis Microwave Plasma Monitoring System For Real-Time Elemental Analysis Microwave Plasma Monitoring System For Real-Time Elemental Analysis The invention apparatus can also be used to monitor for the presence of halogens, sulfur and silicon. Available for thumbnail of Feynman Center (505) 665-9090 Email Microwave Plasma Monitoring System For Real-Time Elemental Analysis There has been invented a process for analyzing ambient air in a microwave induced plasma without use of an additional carrier gas. There has also been invented an apparatus for analyzing ambient air, other sample gas, or nebulized and desolvated liquids wherein a novel arrangement of plasma gas and sample gas conduits is used to enhance dependability of the plasma. This apparatus embodiment of the invention has a concentric arrangement of

386

Extraction of trace metals from fly ash  

DOE Patents (OSTI)

A process for recovering silver, gallium and/or other trace metals from a fine grained industrial fly ash associated with a process for producing phosphorous, the fly ash having a silicate base and containing surface deposits of the trace metals as oxides, chlorides or the like, with the process being carried out by contacting the fly ash with AlCl.sub.3 in an alkali halide melt to react the trace metals with the AlCl.sub.3 to form compositions soluble in the melt and a residue containing the silicate and aluminum oxide or other aluminum precipitate, and separating the desired trace metal or metals from the melt by electrolysis or other separation techniques.

Blander, Milton (Palos Park, IL); Wai, Chien M. (Moscow, ID); Nagy, Zoltan (Woodridge, IL)

1984-01-01T23:59:59.000Z

387

Extraction of trace metals from fly ash  

DOE Patents (OSTI)

A process is described for recovering silver, gallium and/or other trace metals from a fine grained industrial fly ash associated with a process for producing phosphorous. The fly ash has a silicate base and contains surface deposits of the trace metals as oxides, chlorides or the like. The process is carried out by contacting the fly ash with AlCl/sub 3/ in an alkali halide melt to react the trace metals with the AlCl/sub 3/ to form compositions soluble in the melt and a residue containing the silicate and aluminum oxide or other aluminum precipitate, and separating the desired trace metal or metals from the melt by electrolysis or other separation techniques.

Blander, M.; Wai, C.M.; Nagy, Z.

1983-08-15T23:59:59.000Z

388

Accelerating ray tracing using constrained tetrahedralizations  

Science Conference Proceedings (OSTI)

In this paper we introduce the constrained tetrahedralization as a new acceleration structure for ray tracing. A constrained tetrahedralization of a scene is a tetrahedralization that respects the faces of the scene geometry. The closest intersection ...

Ares Lagae; Philip Dutr

2008-06-01T23:59:59.000Z

389

Definition of the n-Trace - CECM  

E-Print Network (OSTI)

Nov 19, 1997 ... Definition of the n-Trace. Suppose $\\Sigma$ is a set of inputs $\\Sigma = \\{\\ alpha_1,\\alpha_2,\\alpha_3.. . Then the set $\\wp(\\Sigma)$...

390

CLOSEOUT REPORT FOR HYBRID SULFUR PRESSURIZED BUTTON CELL TEST FACILITY  

DOE Green Energy (OSTI)

This document is the Close-Out Report for design and partial fabrication of the Pressurized Button Cell Test Facility at Savannah River National Laboratory (SRNL). This facility was planned to help develop the sulfur dioxide depolarized electrolyzer (SDE) that is a key component of the Hybrid Sulfur Cycle for generating hydrogen. The purpose of this report is to provide as much information as possible in case the decision is made to resume research. This report satisfies DOE Milestone M3GSR10VH030107.0. The HyS Cycle is a hybrid thermochemical cycle that may be used in conjunction with advanced nuclear reactors or centralized solar receivers to produce hydrogen by watersplitting. The HyS Cycle utilizes the high temperature (>800 C) thermal decomposition of sulfuric acid to produce oxygen and regenerate sulfur dioxide. The unique aspect of HyS is the generation of hydrogen in a water electrolyzer that is operated under conditions where dissolved sulfur dioxide depolarizes the anodic reaction, resulting in substantial voltage reduction. Low cell voltage is essential for both high thermodynamic efficiency and low hydrogen cost. Sulfur dioxide is oxidized at the anode, producing sulfuric acid that is sent to the high temperature acid decomposition portion of the cycle. Sulfur dioxide from the decomposer is cycled back to electrolyzers. The electrolyzer cell uses the membrane electrode assembly (MEA) concept. Anode and cathode are formed by spraying a catalyst, typically platinized carbon, on both sides of a Proton Exchange Membrane (PEM). SRNL has been testing SDEs for several years including an atmospheric pressure Button Cell electrolyzer (2 cm{sup 2} active area) and an elevated temperature/pressure Single Cell electrolyzer (54.8 cm{sup 2} active area). SRNL tested 37 MEAs in the Single Cell electrolyzer facility from June 2005 until June 2009, when funding was discontinued. An important result of the final months of testing was the development of a method that prevents the formation of a sulfur layer previously observed in MEAs used in the Hybrid Sulfur Cycle electrolyzer. This result is very important because the sulfur layer increased cell voltage and eventually destroyed the MEA that is the heart of the cell. Steimke and Steeper [2005, 2006, 2007, 2008] reported on testing in the Single Cell Electrolyzer test facility in several periodic reports. Steimke et. al [2010] issued a final facility close-out report summarizing all the testing in the Single Cell Electrolyzer test facility. During early tests, significant deterioration of the membrane occurred in 10 hours or less; the latest tests ran for at least 200 hours with no sign of deterioration. Ironically, the success with the Single Cell electrolyzer meant that it became dedicated to long runs and not available for quick membrane evaluations. Early in this research period, the ambient pressure Button Cell Electrolyzer test facility was constructed to quickly evaluate membrane materials. Its small size allowed testing of newly developed membranes that typically were not available in sizes large enough to test in the Single Cell electrolyzer. The most promising membranes were tested in the Single Cell Electrolyzer as soon as sufficient large membranes could be obtained. However, since the concentration of SO{sub 2} gas in sulfuric acid decreases rapidly with increasing temperature, the ambient pressure Button Cell was no longer able to achieve the operating conditions needed to evaluate the newer improved high temperature membranes. Significantly higher pressure operation was required to force SO{sub 2} into the sulfuric acid to obtain meaningful concentrations at increased temperatures. A high pressure (200 psig), high temperature (120 C) Button Cell was designed and partially fabricated just before funding was discontinued in June 2009. SRNL completed the majority of the design of the test facility, including preparation of a process and instrument drawing (P&ID) and preliminary designs for the major components. SRNL intended to complete the designs and procu

Steeper, T.

2010-09-15T23:59:59.000Z

391

Commercial Alloys for Sulfuric Acid Vaporization in Thermochemical Hydrogen Cycles  

DOE Green Energy (OSTI)

Most thermochemical cycles being considered for producing hydrogen include a processing stream in which dilute sulfuric acid is concentrated, vaporized and then decomposed over a catalyst. The sulfuric acid vaporizer is exposed to highly aggressive conditions. Liquid sulfuric acid will be present at a concentration of >96 wt% (>90 mol %) H2SO4 and temperatures exceeding 400oC [Brown, et. al, 2003]. The system will also be pressurized, 0.7-3.5 MPa, to keep the sulfuric acid in the liquid state at this temperature and acid concentration. These conditions far exceed those found in the commercial sulfuric acid generation, regeneration and handling industries. Exotic materials, e.g. ceramics, precious metals, clad materials, etc., have been proposed for this application [Wong, et. al., 2005]. However, development time, costs, reliability, safety concerns and/or certification issues plague such solutions and should be considered as relatively long-term, optimum solutions. A more cost-effective (and relatively near-term) solution would be to use commercially-available metallic alloys to demonstrate the cycle and study process variables. However, the corrosion behavior of commercial alloys in sulfuric acid is rarely characterized above the natural boiling point of concentrated sulfuric acid (~250oC at 1 atm). Therefore a screening study was undertaken to evaluate the suitability of various commercial alloys for concentration and vaporization of high-temperature sulfuric acid. Initially alloys were subjected to static corrosion tests in concentrated sulfuric acid (~95-97% H2SO4) at temperatures and exposure times up to 200oC and 480 hours, respectively. Alloys with a corrosion rate of less than 5 mm/year were then subjected to static corrosion tests at a pressure of 1.4 MPa and temperatures up to 375oC. Exposure times were shorter due to safety concerns and ranged from as short as 5 hours up to 144 hours. The materials evaluated included nickel-, iron- and cobalt-based commercial alloys. The corrosion rates in these tests are reported and how they may or may not relate to the corrosion behavior in an operating thermochemical cycle is discussed.

Thomas M. Lillo; Karen M. Delezene-Briggs

2005-10-01T23:59:59.000Z

392

Process for removal of sulfur compounds from fuel gases  

DOE Patents (OSTI)

Fuel gases such as those produced in the gasification of coal are stripped of sulfur compounds and particulate matter by contact with molten metal salt. The fuel gas and salt are intimately mixed by passage through a venturi or other constriction in which the fuel gas entrains the molten salt as dispersed droplets to a gas-liquid separator. The separated molten salt is divided into a major and a minor flow portion with the minor flow portion passing on to a regenerator in which it is contacted with steam and carbon dioxide as strip gas to remove sulfur compounds. The strip gas is further processed to recover sulfur. The depleted, minor flow portion of salt is passed again into contact with the fuel gas for further sulfur removal from the gas. The sulfur depleted, fuel gas then flows through a solid absorbent for removal of salt droplets. The minor flow portion of the molten salt is then recombined with the major flow portion for feed to the venturi.

Moore, Raymond H. (Richland, WA); Stegen, Gary E. (Richland, WA)

1978-01-01T23:59:59.000Z

393

ADDITIVE TESTING FOR IMPROVED SULFUR RETENTION: PRELIMINARY REPORT  

SciTech Connect

The Savannah River National Laboratory is collaborating with Alfred University to evaluate the potential for additives in borosilicate glass to improve sulfur retention. This preliminary report provides further background on the incorporation of sulfur in glass and outlines the experiments that are being performed by the collaborators. A simulated waste glass composition has been selected for the experimental studies. The first phase of experimental work will evaluate the impacts of BaO, PbO, and V{sub 2}O{sub 5} at concentrations of 1.0, 2.0, and 5.0 wt % on sulfate retention in simulated high level waste borosilicate glass. The second phase of experimental work will evaluate the effects of time at the melt temperature on sulfur retention. The resulting samples will be characterized to determine the amount of sulfur remaining as well as to identify the formation of any crystalline phases. The results will be used to guide the future selection of frits and glass forming chemicals in vitrifying Department of Energy wastes containing high sulfur concentrations.

Amoroso, J.; Fox, K.

2011-09-07T23:59:59.000Z

394

Process and system for removing sulfur from sulfur-containing gaseous streams  

DOE Patents (OSTI)

A multi-stage UCSRP process and system for removal of sulfur from a gaseous stream in which the gaseous stream, which contains a first amount of H.sub.2S, is provided to a first stage UCSRP reactor vessel operating in an excess SO.sub.2 mode at a first amount of SO.sub.2, producing an effluent gas having a reduced amount of SO.sub.2, and in which the effluent gas is provided to a second stage UCSRP reactor vessel operating in an excess H.sub.2S mode, producing a product gas having an amount of H.sub.2S less than said first amount of H.sub.2S.

Basu, Arunabha (Aurora, IL); Meyer, Howard S. (Hoffman Estates, IL); Lynn, Scott (Pleasant Hill, CA); Leppin, Dennis (Chicago, IL); Wangerow, James R. (Medinah, IL)

2012-08-14T23:59:59.000Z

395

Low-quality natural gas sulfur removal/recovery: Task 2. Topical report, September 30, 1992--August 29, 1993  

Science Conference Proceedings (OSTI)

The primary purpose of this Task 2 Report is to present conceptual designs developed to treat a large portion of proven domestic natural gas reserves which are low quality. The conceptual designs separate hydrogen sulfide and large amounts of carbon dioxide (>20%) from methane, convert hydrogen sulfide to elemental sulfur, produce a substantial portion of the carbon dioxide as EOR or food grade CO{sub 2}, and vent residual CO{sub 2} virtually free of contaminating sulfur containing compounds. A secondary purpose of this Task 2 Report is to review existing gas treatment technology and identify existing commercial technologies currently used to treat large volumes of low quality natural gas with high acid content. Section II of this report defines low quality gas and describes the motivation for seeking technology to develop low quality gas reserves. The target low quality gas to be treated with the proposed technology is identified, and barriers to the production of this gas are reviewed. Section III provides a description of the Controlled Freeze Zone (CFG)-CNG technologies, their features, and perceived advantages. The three conceptual process designs prepared under Task 2 are presented in Section IV along with the design basis and process economics. Section V presents an overview of existing gas treatment technologies, organized into acid gas removal technology and sulfur recovery technology.

Cook, W.J.; Neyman, M.; Brown, W. [Acrion Technologies, Inc., Cleveland, OH (United States); Klint, B.W.; Kuehn, L.; O`Connell, J.; Paskall, H.; Dale, P. [Bovar, Inc., Calgary, Alberta (Canada)

1993-08-01T23:59:59.000Z

396

Compound and Elemental Analysis At Central Nevada Seismic Zone Region  

Open Energy Info (EERE)

Nevada Nevada Seismic Zone Region (Coolbaugh, Et Al., 2010) Exploration Activity Details Location Central Nevada Seismic Zone Geothermal Region Exploration Technique Compound and Elemental Analysis Activity Date Usefulness useful DOE-funding Unknown Notes "This second paper provides more detailed documentation on water and rock geochemistries and describes diagnostic major and trace element ratios and concentrations that can be used to distinguish tufa columns formed from thermal waters from those that formed from non-thermal waters." "In addition to providing a potentially diagnostic lithogeochemical tool for geothermal exploration, the analysis of lithium and other elements in tufa deposits could serve as exploration guides for hot spring lithium

397

Compound and Elemental Analysis At Northern Basin & Range Region  

Open Energy Info (EERE)

(Coolbaugh, Et Al., 2010) (Coolbaugh, Et Al., 2010) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Compound and Elemental Analysis At Northern Basin & Range Region (Coolbaugh, Et Al., 2010) Exploration Activity Details Location Northern Basin and Range Geothermal Region Exploration Technique Compound and Elemental Analysis Activity Date Usefulness useful DOE-funding Unknown Notes "This second paper provides more detailed documentation on water and rock geochemistries and describes diagnostic major and trace element ratios and concentrations that can be used to distinguish tufa columns formed from thermal waters from those that formed from non-thermal waters." "In addition to providing a potentially diagnostic lithogeochemical tool for

398

Trace metals in heavy crude oils and tar sand bitumens  

SciTech Connect

Fe, Ni, and V are considered trace impurities in heavy crude oils and tar sand bitumens. In order to understand the importance of these metals, we have examined several properties: (1) bulk metals levels, (2) distribution in separated fractions, (3) size behavior in feeds and during processing, (4) speciation as a function of size, and (5) correlations with rheological properties. Some of the results of these studies show: (1) V and Ni have roughly bimodal size distributions, (2) groupings were seen based on location, size distribution, and Ni/V ratio of the sample, (3) Fe profiles are distinctively different, having a unimodal distribution with a maximum at relatively large molecular size, (4) Fe concentrations in the tar sand bitumens suggest possible fines solubilization in some cases, (5) SARA separated fractions show possible correlations of metals with asphaltene properties suggesting secondary and tertiary structure interactions, and (6) ICP-MS examination for soluble ultra-trace metal impurities show the possibility of unexpected elements such as U, Th, Mo, and others at concentrations in the ppB to ppM range. 39 refs., 13 figs., 5 tabs.

Reynolds, J.G.

1990-11-28T23:59:59.000Z

399

Process for oxidation of hydrogen halides to elemental halogens  

DOE Patents (OSTI)

An improved process for generating an elemental halogen selected from chlorine, bromine or iodine, from a corresponding hydrogen halide by absorbing a molten salt mixture, which includes sulfur, alkali metals and oxygen with a sulfur to metal molar ratio between 0.9 and 1.1 and includes a dissolved oxygen compound capable of reacting with hydrogen halide to produce elemental halogen, into a porous, relatively inert substrate to produce a substrate-supported salt mixture. Thereafter, the substrate-supported salt mixture is contacted (stage 1) with a hydrogen halide while maintaining the substrate-supported salt mixture during the contacting at an elevated temperature sufficient to sustain a reaction between the oxygen compound and the hydrogen halide to produce a gaseous elemental halogen product. This is followed by purging the substrate-supported salt mixture with steam (stage 2) thereby recovering any unreacted hydrogen halide and additional elemental halogen for recycle to stage 1. The dissolved oxygen compound is regenerated in a high temperature (stage 3) and an optical intermediate temperature stage (stage 4) by contacting the substrate-supported salt mixture with a gas containing oxygen whereby the dissolved oxygen compound in the substrate-supported salt mixture is regenerated by being oxidized to a higher valence state.

Lyke, Stephen E. (Middleton, WI)

1992-01-01T23:59:59.000Z

400

Why sequence Sulfur cycling in the Frasassi aquifer?  

NLE Websites -- All DOE Office Websites (Extended Search)

sulfur cycling in the Frasassi aquifer? sulfur cycling in the Frasassi aquifer? The terrestrial subsurface remains one of the least explored microbial habitats on earth, and is critical for understanding pollutant migration and attenuation, subsurface processes such as limestone dissolution (affecting porosity), and the search for life elsewhere in the solar system and beyond. The deep and sulfidic Frasassi aquifer (of Ancona, Italy) has emerged as a model system for studying sulfur cycling in the terrestrial subsurface, and this sequencing project has relevance for developing applications for wastewater treatment and capabilities relevant for radionuclide, metal and organic pollutant remediation that can be applied at environments at DOE subsurface sites. Principal Investigators: Jennifer Macalady, Penn State University

Note: This page contains sample records for the topic "trace elements 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

Sodium/Phosphorus-Sulfur Cells II. Phase Equilibria  

NLE Websites -- All DOE Office Websites (Extended Search)

II. Phase Equilibria II. Phase Equilibria Title Sodium/Phosphorus-Sulfur Cells II. Phase Equilibria Publication Type Journal Article Year of Publication 1996 Authors Ridgway, Paul L., Frank R. McLarnon, and John S. Newman Journal Journal of the Electrochemistry Society Volume 143 Issue 2 Pagination 412-417 Keywords 25 ENERGY STORAGE, 36 MATERIALS SCIENCE, ALUMINIUM OXIDES, equilibrium, performance, PHASE DIAGRAMS, PHOSPHIDES, PHOSPHORUS ADDITIONS, SODIUM COMPOUNDS, SODIUM SULFIDES, SODIUM-SULFUR BATTERIES Abstract Equilibrium open-circuit cell voltage data from a sodium/{beta}{double_prime}-alumina/phosphorus-sulfur cell utilizing P/S ratios of 0, 0.143, and 0.332 and a sodium atom fraction ranging from 0 to 0.4 were interpreted to construct ternary phase diagrams of the Na-P-S ternary system at 350 and 400 C.

402

HYBRID SULFUR ELECTROLYZER DEVELOPMENT FY09 SECOND QUARTER REPORT  

DOE Green Energy (OSTI)

The primary objective of the DOE-NE Nuclear Hydrogen Initiative (NHI) is to develop the nuclear hydrogen production technologies necessary to produce hydrogen at a cost competitive with other alternative transportation fuels. The focus of the NHI is on thermochemical cycles and high temperature electrolysis that can be powered by heat from high temperature gas reactors. The Savannah River National Laboratory (SRNL) has been tasked with the primary responsibility to perform research and development in order to characterize, evaluate and develop the Hybrid Sulfur (HyS) thermochemical process. This report documents work during the first quarter of Fiscal Year 2009, for the period between January 1, 2009 and March 31, 2009. The HyS Process is a two-step hybrid thermochemical cycle that is part of the 'Sulfur Family' of cycles. As a sulfur cycle, it uses high temperature thermal decomposition of sulfuric acid to produce oxygen and to regenerate the sulfur dioxide reactant. The second step of the process uses a sulfur dioxide depolarized electrolyzer (SDE) to split water and produce hydrogen by electrochemically reacting sulfur dioxide with H{sub 2}O. The SDE produces sulfuric acid, which is then sent to the acid decomposer to complete the cycle. The DOE NHI program is developing the acid decomposer at Sandia National Laboratory for application to both the HyS Process and the Sulfur Iodine Cycle. The SDE is being developed at SRNL. During FY05 and FY06, SRNL designed and conducted proof-of-concept testing for a SDE using a low temperature, PEM fuel cell-type design concept. The advantages of this design concept include high electrochemical efficiency, small footprint and potential for low capital cost, characteristics that are crucial for successful implementation on a commercial scale. During FY07, SRNL extended the range of testing of the SDE to higher temperature and pressure, conducted a 100-hour longevity test with a 60-cm{sup 2} single cell electrolyzer, and designed and built a larger, multi-cell stack electrolyzer. During FY08, SRNL continued SDE development, including development and successful testing of a three-cell electrolyzer stack with a rated capacity of 100 liters per hour. The HyS program for FY09 program will address improving SDE performance by focusing on preventing or minimizing sulfur deposition inside the cell caused by SO{sub 2} crossover, reduction of cell voltage for improved efficiency, an extension of cell operating lifetime. During FY09 a baseline technology development program is being conducted to address each of these issues. Button-cell (2-cm{sup 2}) and single cell (60-cm{sup 2}) SDEs will be fabricated and tested. A pressurized button-cell test facility will be designed and constructed to facilitate addition testing. The single cell test facility will be upgraded for unattended operation, and later for operation at higher temperature and pressure. Work will continue on development of the Gas Diffusion Electrode (GDE), or Gap Cell, as an alternative electrolyzer design approach that is being developed under subcontract with industry partner Giner Electrochemical Systems. If successful, it could provide an alternative means of preventing sulfur crossover through the proton exchange membrane, as well as the possibility for higher current density operation based on more rapid mass transfer in a gas-phase anode. Promising cell components will be assembled into membrane electrode assemblies (MEAs) and tested in the single cell test facility. Upon modification for unattended operation, test will be conducted for 200 hours or more. Both the button-cell and modified single cell facility will be utilized to demonstrate electrolyzer operation without sulfur build-up limitations, which is a Level 1 Milestone.

Herman, D; David Hobbs, D; Hector Colon-Mercado, H; Timothy Steeper, T; John Steimke, J; Mark Elvington, M

2009-04-15T23:59:59.000Z

403

Preliminary Investigation of Sulfur Loading in Hanford LAW Glass  

SciTech Connect

A preliminary estimate was developed for loading limits for high-sulfur low-activity waste (LAW) feeds that will be vitrified into borosilicate glass at the Hanford Site in the waste-cleanup effort. Previous studies reported in the literature were consulted to provide a basis for the estimate. The examination of previous studies led to questions about sulfur loading in Hanford LAW glass, and scoping tests were performed to help answer these questions. These results of these tests indicated that a formulation approach developed by Vienna and colleagues shows promise for maximizing LAW loading in glass. However, there is a clear need for follow-on work. The potential for significantly lowering the amount of LAW glass produced at Hanford (after the initial phase of processing) because of higher sulfur tolerances may outweigh the cost and effort required to perform the necessary testing.

Vienna, John D.; Hrma, Pavel R.; Buchmiller, William C.; Ricklefs, Joel S.

2004-04-01T23:59:59.000Z

404

Prius: generic hybrid trace compression for wireless sensor networks  

Science Conference Proceedings (OSTI)

Several diagnostic tracing techniques (e.g., event, power, and control-flow tracing) have been proposed for run-time debugging and postmortem analysis of wireless sensor networks (WSNs). Traces generated by such techniques can become large, defying the ... Keywords: compression, sensor networks, tracing

Vinaitheerthan Sundaram; Patrick Eugster; Xiangyu Zhang

2012-11-01T23:59:59.000Z

405

Investigation into the effects of trace coal syn gas species on the performance of solid oxide fuel cell anodes, PhD. thesis, Russ College of Engineering and Technology of Ohio University  

DOE Green Energy (OSTI)

Coal is the United States most widely used fossil fuel for the production of electric power. Coals availability and cost dictates that it will be used for many years to come in the United States for power production. As a result of the environmental impact of burning coal for power production more efficient and environmentally benign power production processes using coal are sought. Solid oxide fuel cells (SOFCs) combined with gasification technologies represent a potential methodology to produce electric power using coal in a much more efficient and cleaner manner. It has been shown in the past that trace species contained in coal, such as sulfur, severely degrade the performance of solid oxide fuel cells rendering them useless. Coal derived syngas cleanup technologies have been developed that efficiently remove sulfur to levels that do not cause any performance losses in solid oxide fuel cells. The ability of these systems to clean other trace species contained in syngas is not known nor is the effect of these trace species on the performance of solid oxide fuel cells. This works presents the thermodynamic and diffusion transport simulations that were combined with experimental testing to evaluate the effects of the trace species on the performance of solid oxide fuel cells. The results show that some trace species contained in coal will interact with the SOFC anode. In addition to the transport and thermodynamic simulations that were completed experimental tests were completed investigating the effect of HCl and AsH3 on the performance of SOFCs.

Trembly, J.P.

2007-06-01T23:59:59.000Z

406

Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program  

Alternative Fuels and Advanced Vehicles Data Center (EERE)

Tier 2 Vehicle and Tier 2 Vehicle and Gasoline Sulfur Program to someone by E-mail Share Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Facebook Tweet about Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Twitter Bookmark Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Google Bookmark Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Delicious Rank Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Digg Find More places to share Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on AddThis.com... More in this section... Federal State Advanced Search All Laws & Incentives Sorted by Type Tier 2 Vehicle and Gasoline Sulfur Program

407

Proposed use of antimonyl sulfate in a sulfuric-acid cycle  

DOE Green Energy (OSTI)

A proposed use of antimonyl sulfate in a sulfuric acid thermochemical hydrogen cycle is outlined. The principal advantage would be the separate evolution of sulfur dioxide and oxygen in high temperature steps.

Jones, W.M.

1982-01-01T23:59:59.000Z

408

A design strategy applied to sulfur resistant lean NOx̳ automotive catalysts  

E-Print Network (OSTI)

Catalyst poisoning due to sulfur compounds derived from fuel sulfur presents a major challenge, intractable thus far, to development of many advanced technologies for automotive catalysts such as the lean NOx, trap. Under ...

Tang, Hairong

2005-01-01T23:59:59.000Z

409

System for adding sulfur to a fuel cell stack system for improved fuel cell stability  

DOE Patents (OSTI)

A system for adding sulfur to a fuel cell stack, having a reformer adapted to reform a hydrocarbon fuel stream containing sulfur contaminants, thereby providing a reformate stream having sulfur; a sulfur trap fluidly coupled downstream of the reformer for removing sulfur from the reformate stream, thereby providing a desulfurized reformate stream; and a metering device in fluid communication with the reformate stream upstream of the sulfur trap and with the desulfurized reformate stream downstream of the sulfur trap. The metering device is adapted to bypass a portion of the reformate stream to mix with the desulfurized reformate stream, thereby producing a conditioned reformate stream having a predetermined sulfur concentration that gives an acceptable balance of minimal drop in initial power with the desired maximum stability of operation over prolonged periods for the fuel cell stack.

Mukerjee, Subhasish (Pittsford, NY); Haltiner, Jr., Karl J (Fairport, NY); Weissman, Jeffrey G. (West Henrietta, NY)

2012-03-06T23:59:59.000Z

410

Polyol-free synthesis of uniformly dispersed Pt/graphene oxide electrocatalyst by sulfuric acid treatment  

Science Conference Proceedings (OSTI)

Polyol-free synthesis of highly loaded Pt catalysts on sulfuric-acid-treated graphene oxide (SGO) was reported. Sulfuric acid treatment increased the surface hydroxyl groups on graphene oxide (GO), which contributed to the reduction of Pt precursors ...

Tae Kyu Lee, Hyang Jin Park, Min Ki Kwon, Ju Hae Jung, Junbom Kim, Seung Hyun Hur

2012-01-01T23:59:59.000Z

411

Concentrations and Origins of Atmospheric Lead and Other Trace Species at a Rural Site in Northern China  

E-Print Network (OSTI)

grade HNO3 (6 mL) and HCl (2 mL) for 40 min, using a microwave sample digestion system (PerkinElmer Life factor of 2 is applied to the Al concentration. An inductively coupled plasma mass spectrometer (ICP), The fate of trace elements during coal combustion and gasification: an overview, Fuel, 72, 731-736. Díaz

Dickerson, Russell R.

412

Trace metal speciation in saline waters affected by geothermal brines. [GEOCHEM  

DOE Green Energy (OSTI)

A description is given of the chemical equilibrium computer program GEOCHEM, which has been developed to calculate trace element speciation in soil, irrigation, drainage, or Salton Sea waters affected by geothermal brine. GEOCHEM is applied to irrigation water-brine mixtures and to Salton Sea water-brine mixtures in order to compute the chemical speciation of the elements Cd, Cu, Hg, Ni, Pb, and Zn, along with the oxyanions of As and B. The results suggest that the computer simulation can have an important effect on a program for managing brine spills. Appendices include published papers on related research.

Sposito, G.; Page, A.L.

1977-11-01T23:59:59.000Z

413

SYNTHESIS OF SULFUR-BASED WATER TREATMENT AGENT FROM SULFUR DIOXIDE WASTE STREAMS  

Science Conference Proceedings (OSTI)

Absorption of sulfur dioxide from a simulated flue gas was investigated for the production of polymeric ferric sulfate (PFS), a highly effective coagulant useful in treatment of drinking water and wastewater. The reaction for PFS synthesis took place near atmospheric pressure and at temperatures of 30-80 C. SO{sub 2} removal efficiencies greater than 90% were achieved, with ferrous iron concentrations in the product less than 0.1%. A factorial analysis of the effect of temperature, oxidant dosage, SO{sub 2} concentration, and gas flow rate on SO{sub 2} removal efficiency was carried out, and statistical analyses are conducted. The solid PFS was also characterized with different methods. Characterization results have shown that PFS possesses both crystalline and non-crystalline structure. The kinetics of reactions among FeSO{sub 4} {center_dot} 7H{sub 2}O, NaHSO{sub 3} and NaClO{sub 3} was investigated. Characterizations of dry PFS synthesized from SO{sub 2} show the PFS possesses amorphous structure, which is desired for it to be a good coagulant in water and wastewater treatment. A series of lab-scale experiments were conducted to evaluate the performance of PFS synthesized from waste sulfur dioxide, ferrous sulfate and sodium chlorate. The performance assessments were based on the comparison of PFS and other conventional and new coagulants for the removal of turbidity and arsenic under different laboratory coagulant conditions. Pilot plant studies were conducted at Des Moines Water Works in Iowa and at the City of Savannah Industrial and Domestic (I&D) Water Treatment Plant in Port Wentworth, Georgia. PFS performances were compared with those of conventional coagulants. The tests in both water treatment plants have shown that PFS is, in general, comparable or better than other coagulants in removal of turbidity and organic substances. The corrosion behavior of polymeric ferric sulfate (PFS) prepared from SO{sub 2} and ferric chloride (FC) were compared. Results showed that both temperature and concentration of the coagulants substantially impact corrosion rates. The corrosion rates increased with the increase of temperature and concentration. The results from a scanning electron microscope (SEM) showed that chloride caused more serious pitting than sulfate anion on both aluminum and steel specimens. Although SEM confirmed the existence of pitting corrosion, the results of weight loss indicated that the uniform corrosion predominate the corrosion mechanism, and pitting corrosion played a less important role. The test proved that PFS was less corrosive than FC, which may lead to the large-scale application of PFS in waste treatment. The kinetics of the new desulfurization process has been studied. The study results provide the theoretical guidance for improving sulfur removal efficiency and controlling the quality of PFS.

Robert C. Brown; Maohong Fan; Adrienne Cooper

2004-11-01T23:59:59.000Z

414

Investigations on the sediment chronology and trace metal accumulation in Sabine-Neches estuary, Beaumont, Texas  

E-Print Network (OSTI)

The accumulation rates of sediments and trace metals (Co, Cr, Cu, Ni, Pb, Zn) were measured along with the concentrations of Al, Fe, Mn and organic carbon in four sediment cores from Sabine-Neches estuary, near Beaumont, Texas. A reliable geochronology of sediments and reconstruction of the history of trace metal inputs into this shallow estuarine environment was possible because the 239,240pu profiles closely tracked the bomb fallout history into the environment. The sedimentation rate was estimated to be about 4-5 mm/yr. Due to the very low and variable activities of excess 21OPb in the sediments, the 21OPb dating method did not prove to be very useful in the study area. One difficulty had to do with the large variability of grain size parameters in the sediments. The amount of fines varied from 90% within a single core. The activities of excess 21OPb and the concentrations of Al, Fe, organic carbon, and trace metals varied as a function of the amount of fine particles. 21OPb at the bottom of the sediment cores was in secular equilibrium with 226Ra, 23OTh, and 234U in some cores, while in others, this was not the case. The reasons for disagreement between 21OPb and 226Ra concentrations at depth were investigated. The mixing rates of surface sediments were low and was about 0.16-0.40 cm2yr-1. Down core variations of aluminum normalized enrichment factors for trace metals demonstrated that, since 1860, the sediments of this estuary have remained relatively "pristine" with respect to trace metal concentrations. While the concentrations of Pb and Zn in some sections of the sediment column were slightly enriched, Co, Cr, Cu, and Ni were depleted in all sediment cores analyzed. No significant enrichment of light rare earth elements was observed. Enrichment might have been expected from inputs of cracking catalysts used in refineries. Therefore REEs could not be used as non-steady tracers. The lack of strong enrichment of trace metals, light rare earth elements, and low inventories of radioisotopes could be a result of the short residence time of the estuarine water, long removal residence times of trace metals and radioactive elements in the water column, low salinity conditions, and possibly, complexation of these metals with dissolved organic matter.

Ravichandran, Mahalingam

1994-01-01T23:59:59.000Z

415

Flue Gas Sulfuric Acid Measurement Method Improvements: Second Interim Report, December 2000  

Science Conference Proceedings (OSTI)

The objective of this project is to improve the ability of electric utilities with coal and oil-fired power plants to measure and report sulfuric emissions. Most coal and oil-fired utility boilers will trigger Toxic Release Inventory (TRI) reporting for sulfuric acid. The Controlled Condensation System (CCS) method for measuring flue gas sulfuric acid concentrations is believed to provide one of the best methods for measuring sulfuric acid in flue gas. However, there are situations where the CCS method m...

2000-12-05T23:59:59.000Z

416

South Dakota No 2 Diesel Ultra Low Sulfur Less than 15 ppm Retail ...  

U.S. Energy Information Administration (EIA)

South Dakota No 2 Diesel Ultra Low Sulfur Less than 15 ppm Retail Sales by Refiners (Thousand Gallons per Day)

417

Tracing Noble Gas Radionuclides in the Environment  

E-Print Network (OSTI)

Trace analysis of radionuclides is an essential and versatile tool in modern science and technology. Due to their ideal geophysical and geochemical properties, long-lived noble gas radionuclides, in particular, 39Ar (t1/2 = 269 yr), 81Kr (t1/2 = 2.3x10^5 yr) and 85Kr (t1/2 = 10.8 yr), have long been recognized to have a wide range of important applications in Earth sciences. In recent years, significant progress has been made in the development of practical analytical methods, and has led to applications of these isotopes in the hydrosphere (tracing the flow of groundwater and ocean water). In this article, we introduce the applications of these isotopes and review three leading analytical methods: Low-Level Counting (LLC), Accelerator Mass Spectrometry (AMS) and Atom Trap Trace Analysis (ATTA).

P. Collon; W. Kutschera; Z. -T. Lu

2004-02-11T23:59:59.000Z

418

SUSTAINABLE DEVELOPMENT IN KAZAKHASTAN: USING OIL AND GAS PRODUCTION BY-PRODUCT SULFUR FOR COST-EFFECTIVE SECONDARY END-USE PRODUCTS.  

SciTech Connect

The Republic of Kazakhstan is continuing to develop its extensive petroleum reserves in the Tengiz region of the northeastern part of the Caspian Sea. Large quantities of by-product sulfur are being produced as a result of the removal of hydrogen sulfide from the oil and gas produced in the region. Lack of local markets and economic considerations limit the traditional outlets for by-product sulfur and the buildup of excess sulfur is a becoming a potential economic and environmental liability. Thus, new applications for re-use of by-product sulfur that will benefit regional economies including construction, paving and waste treatment are being developed. One promising application involves the cleanup and treatment of mercury at a Kazakhstan chemical plant. During 19 years of operation at the Pavlodar Khimprom chlor-alkali production facility, over 900 tons of mercury was lost to the soil surrounding and beneath the buildings. The Institute of Metallurgy and Ore Benefication (Almaty) is leading a team to develop and demonstrate a vacuum-assisted thermal process to extract the mercury from the soil and concentrate it as pure, elemental mercury, which will then be treated using the Sulfur Polymer Stabilization/Solidification (SPSS) process. The use of locally produced sulfur will recycle a low-value industrial by-product to treat hazardous waste and render it safe for return to the environment, thereby helping to solve two problems at once. SPSS chemically stabilizes mercury to mercuric sulfide, which has a low vapor pressure and low solubility, and then physically encapsulates the material in a durable, monolithic solid sulfur polymer matrix. Thus, mercury is placed in a solid form very much like stable cinnabar, the form in which it is found in nature. Previous research and development has shown that the process can successfully encapsulate up to 33 wt% mercury in the solid form, while still meeting very strict regulatory standards for leachable mercury (0.025 mg/l in the Toxicity Characteristic Leaching Procedure). The research and development to deploy Kazakhstan recycled sulfur for secondary applications described in this paper is being conducted with support from the International Science and Technology Center (ISTC) and the U.S. Department of Energy Initiatives for Proliferation Prevention (DOE IPP).

KALB, P.D.; VAGIN, S.; BEALL, P.W.; LEVINTOV, B.L.

2004-09-25T23:59:59.000Z

419

New improved standard for electron probe determination of organic sulfur in fossil fuels  

Science Conference Proceedings (OSTI)

This paper reports on petroleum coke that is stable under an electron beam and contains a uniform sulfur content. Hence, it is a suitable standard for analysis of organic sulfur content of coal. It should be as applicable for analysis of organic sulfur in other fossil fuels. This standard is available for distribution.

Harris, L.A.; Raymond, R. Jr.; Gooley, R.

1980-01-01T23:59:59.000Z

420

Superconductivity at 35 K in Graphite-Sulfur Composites  

E-Print Network (OSTI)

We report magnetization measurements performed on graphitesulfur composites which demonstrate a clear superconducting behavior below the critical temperature Tc0 = 35 K. The Meissner-Ochsenfeld effect, screening supercurrents, and magnetization hysteresis loops characteristic of type-II superconductors were measured. The results indicate that the superconductivity occurs in a small sample fraction, possibly related to the sample surface.

R. Ricardo Da Silva; J. H. S. Torres; Y. Kopelevich

2001-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "trace elements 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.


421

The Hybrid Sulfur Cycle for Nuclear Hydrogen Production  

DOE Green Energy (OSTI)

Two Sulfur-based cycles--the Sulfur-Iodine (SI) and the Hybrid Sulfur (HyS)--have emerged as the leading thermochemical water-splitting processes for producing hydrogen utilizing the heat from advanced nuclear reactors. Numerous international efforts have been underway for several years to develop the SI Cycle, but development of the HyS Cycle has lagged. The purpose of this paper is to discuss the background, current status, recent development results, and the future potential for this thermochemical process. Savannah River National Laboratory (SRNL) has been supported by the U.S. Department of Energy Office of Nuclear Energy, Science, and Technology since 2004 to evaluate and to conduct research and development for the HyS Cycle. Process design studies and flowsheet optimization have shown that an overall plant efficiency (based on nuclear heat converted to hydrogen product, higher heating value basis) of over 50% is possible with this cycle. Economic studies indicate that a nuclear hydrogen plant based on this process can be economically competitive, assuming that the key component, the sulfur dioxide-depolarized electrolyzer, can be successfully developed. SRNL has recently demonstrated the use of a proton-exchange-membrane electrochemical cell to perform this function, thus holding promise for economical and efficient hydrogen production.

Summers, William A.; Gorensek, Maximilian B.; Buckner, Melvin R.

2005-09-08T23:59:59.000Z

422

Revisit Carbon/Sulfur Composite for Li-S Batteries  

SciTech Connect

To correlate the carbon properties e.g. surface area and porous structure, with the electrochemical behaviors of carbon/sulfur (C/S) composite cathodes for lithium-sulfur (Li-S) batteries, four different carbon frameworks including Ketjen Black (KB, high surface area and porous), Graphene (high surface area and nonporous), Acetylene Black (AB, low surface area and nonporous) and Hollow Carbon Nano Sphere (HCNS, low surface area and porous) are employed to immobilize sulfur (80 wt.%). It has been revealed that high surface area of carbon improves the utilization rate of active sulfur and decreases the real current density during the electrochemical reactions. Accordingly, increased reversible capacities and reduced polarization are observed for high surface area carbon hosts such as KB/S and graphene/S composites. The porous structure of KB or HCNS matrix promotes the long-term cycling stability of C/S composites but only at relatively low rate (0.2 C). Once the current density increases, the pore effect completely disappears and all Li-S batteries show similar trend of capacity degradation regardless of the different carbon hosts used in the cathodes. The reason has been assigned to the formation of reduced amount of irreversible Li2S on the cathode as well as shortened time for polysulfides to transport towards lithium anode at elevated current densities. This work provides valuable information for predictive selection on carbon materials to construct C/S composite for practical applications from the electrochemical point of view.

Zheng, Jianming; Gu, Meng; Wagner, Michael J.; Hays, Kevin; Li, Xiaohong S.; Zuo, Pengjian; Wang, Chong M.; Zhang, Jiguang; Liu, Jun; Xiao, Jie

2013-07-23T23:59:59.000Z

423

Sodium and sulfur release and recapture during black liquor burning  

DOE Green Energy (OSTI)

The objective of this study was to provide data on sulfur and sodium volatilization during black liquor burning, and on SO2 capture by solid sodium carbonate and sodium chloride. This data was interpreted and modeled into rate equations suitable for use in computational models for recovery boilers.

Frederick, W.J.; Iisa, K.; Wag, K.; Reis, V.V.; Boonsongsup, L.; Forssen, M.; Hupa, M.

1995-08-01T23:59:59.000Z

424

Vapor-Liquid Partitioning of Sulfuric Acid and Ammonium Sulfate  

Science Conference Proceedings (OSTI)

The quality of water and steam is central to ensuring power plant component availability and reliability. A key part of developing operating cycle chemistry guidelines is an understanding of the impurity distribution between water and steam. This study focused on the partitioning of sulfuric acid and ammonium bisulfate between the liquid and vapor phases.

1999-03-31T23:59:59.000Z

425

Process for removal of sulfur oxides from waste gases  

Science Conference Proceedings (OSTI)

A process for removing sulfur oxides from waste gas is provided. The gas is contacted with a sorbent selected from sodium bicarbonate, trona and activated sodium carbonate and, utilizing an alkaline liquor containing borate ion so as to reduce flow rates and loss of alkalinity, the spent sorbent is regenerated with an alkaline earth metal oxide or hydroxide.

Lowell, P.S.; Phillips, J.L.

1983-05-24T23:59:59.000Z

426

It's Elemental - Isotopes of the Element Magnesium  

NLE Websites -- All DOE Office Websites (Extended Search)

Sodium Sodium Previous Element (Sodium) The Periodic Table of Elements Next Element (Aluminum) Aluminum Isotopes of the Element Magnesium [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 24 78.99% STABLE 25 10.00% STABLE 26 11.01% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 19 4.0 picoseconds Double Proton Emission 100.00% 20 90.8 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission ~ 27.00% 21 122 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 32.60% Electron Capture with delayed Alpha Decay < 0.50%

427

It's Elemental - Isotopes of the Element Potassium  

NLE Websites -- All DOE Office Websites (Extended Search)

Argon Argon Previous Element (Argon) The Periodic Table of Elements Next Element (Calcium) Calcium Isotopes of the Element Potassium [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 39 93.2581% STABLE 40 0.0117% 1.248×10+9 years 41 6.7302% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 32 No Data Available Proton Emission (suspected) No Data Available 33 < 25 nanoseconds Proton Emission No Data Available 34 < 25 nanoseconds Proton Emission No Data Available 35 178 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 0.37% 36 342 milliseconds Electron Capture 100.00%

428

It's Elemental - Isotopes of the Element Oxygen  

NLE Websites -- All DOE Office Websites (Extended Search)

Nitrogen Nitrogen Previous Element (Nitrogen) The Periodic Table of Elements Next Element (Fluorine) Fluorine Isotopes of the Element Oxygen [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 16 99.757% STABLE 17 0.038% STABLE 18 0.205% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 12 1.139×10-21 seconds Proton Emission No Data Available 13 8.58 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 100.00% 14 70.620 seconds Electron Capture 100.00% 15 122.24 seconds Electron Capture 100.00% 16 STABLE - - 17 STABLE - - 18 STABLE - - 19 26.88 seconds Beta-minus Decay 100.00%

429

It's Elemental - Isotopes of the Element Gallium  

NLE Websites -- All DOE Office Websites (Extended Search)

Zinc Zinc Previous Element (Zinc) The Periodic Table of Elements Next Element (Germanium) Germanium Isotopes of the Element Gallium [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 69 60.108% STABLE 71 39.892% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 56 No Data Available Proton Emission (suspected) No Data Available 57 No Data Available Proton Emission (suspected) No Data Available 58 No Data Available Proton Emission (suspected) No Data Available 59 No Data Available Proton Emission (suspected) No Data Available 60 70 milliseconds Electron Capture 98.40%

430

It's Elemental - Isotopes of the Element Sodium  

NLE Websites -- All DOE Office Websites (Extended Search)

Neon Neon Previous Element (Neon) The Periodic Table of Elements Next Element (Magnesium) Magnesium Isotopes of the Element Sodium [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 23 100% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 18 1.3×10-21 seconds Proton Emission 100.00% 19 < 40 nanoseconds Proton Emission No Data Available 20 447.9 milliseconds Electron Capture with delayed Alpha Decay 20.05% Electron Capture 100.00% 21 22.49 seconds Electron Capture 100.00% 22 2.6027 years Electron Capture 100.00% 23 STABLE - - 24 14.997 hours Beta-minus Decay 100.00%

431

It's Elemental - Isotopes of the Element Neon  

NLE Websites -- All DOE Office Websites (Extended Search)

Fluorine Fluorine Previous Element (Fluorine) The Periodic Table of Elements Next Element (Sodium) Sodium Isotopes of the Element Neon [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 20 90.48% STABLE 21 0.27% STABLE 22 9.25% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 16 9×10-21 seconds Double Proton Emission 100.00% 17 109.2 milliseconds Electron Capture with delayed Alpha Decay No Data Available Electron Capture 100.00% Electron Capture with delayed Proton Emission 100.00% 18 1.6670 seconds Electron Capture 100.00% 19 17.22 seconds Electron Capture 100.00% 20 STABLE - -

432

It's Elemental - Isotopes of the Element Copper  

NLE Websites -- All DOE Office Websites (Extended Search)

Nickel Nickel Previous Element (Nickel) The Periodic Table of Elements Next Element (Zinc) Zinc Isotopes of the Element Copper [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 63 69.15% STABLE 65 30.85% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 52 No Data Available Proton Emission No Data Available 53 < 300 nanoseconds Electron Capture No Data Available Proton Emission No Data Available 54 < 75 nanoseconds Proton Emission No Data Available 55 27 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 15.0% 56 93 milliseconds Electron Capture 100.00%

433

It's Elemental - Isotopes of the Element Boron  

NLE Websites -- All DOE Office Websites (Extended Search)

Beryllium Beryllium Previous Element (Beryllium) The Periodic Table of Elements Next Element (Carbon) Carbon Isotopes of the Element Boron [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 10 19.9% STABLE 11 80.1% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 6 No Data Available Double Proton Emission (suspected) No Data Available 7 3.255×10-22 seconds Proton Emission No Data Available Alpha Decay No Data Available 8 770 milliseconds Electron Capture 100.00% Electron Capture with delayed Alpha Decay 100.00% 9 8.439×10-19 seconds Proton Emission 100.00% Double Alpha Decay 100.00%

434

It's Elemental - Isotopes of the Element Tungsten  

NLE Websites -- All DOE Office Websites (Extended Search)

Tantalum Tantalum Previous Element (Tantalum) The Periodic Table of Elements Next Element (Rhenium) Rhenium Isotopes of the Element Tungsten [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 180 0.12% >= 6.6×10+17 years 182 26.50% STABLE 183 14.31% > 1.3×10+19 years 184 30.64% STABLE 186 28.43% > 2.3×10+19 years Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 157 275 milliseconds Electron Capture No Data Available 158 1.25 milliseconds Alpha Decay 100.00% 158m 0.143 milliseconds Isomeric Transition No Data Available Alpha Decay No Data Available 159 7.3 milliseconds Alpha Decay ~ 99.90%

435

It's Elemental - Isotopes of the Element Radon  

NLE Websites -- All DOE Office Websites (Extended Search)

Astatine Astatine Previous Element (Astatine) The Periodic Table of Elements Next Element (Francium) Francium Isotopes of the Element Radon [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Radon has no naturally occurring isotopes. Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 193 1.15 milliseconds Alpha Decay 100.00% 194 0.78 milliseconds Alpha Decay 100.00% 195 6 milliseconds Alpha Decay 100.00% 195m 5 milliseconds Alpha Decay 100.00% 196 4.4 milliseconds Alpha Decay 99.90% Electron Capture ~ 0.10% 197 53 milliseconds Alpha Decay 100.00% 197m 25 milliseconds Alpha Decay 100.00% 198 65 milliseconds Alpha Decay No Data Available

436

It's Elemental - Isotopes of the Element Carbon  

NLE Websites -- All DOE Office Websites (Extended Search)

Boron Boron Previous Element (Boron) The Periodic Table of Elements Next Element (Nitrogen) Nitrogen Isotopes of the Element Carbon [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 12 98.93% STABLE 13 1.07% STABLE Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 8 1.981×10-21 seconds Proton Emission 100.00% Alpha Decay No Data Available 9 126.5 milliseconds Electron Capture 100.00% Electron Capture with delayed Proton Emission 61.60% Electron Capture with delayed Alpha Decay 38.40% 10 19.308 seconds Electron Capture 100.00% 11 20.334 minutes Electron Capture 100.00% 12 STABLE - -

437

It's Elemental - Isotopes of the Element Rhenium  

NLE Websites -- All DOE Office Websites (Extended Search)

Tungsten Tungsten Previous Element (Tungsten) The Periodic Table of Elements Next Element (Osmium) Osmium Isotopes of the Element Rhenium [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Mass Number Natural Abundance Half-life 185 37.40% STABLE 187 62.60% 4.33×10+10 years Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 159 No Data Available No Data Available No Data Available 160 0.82 milliseconds Proton Emission 91.00% Alpha Decay 9.00% 161 0.44 milliseconds Proton Emission 100.00% Alpha Decay <= 1.40% 161m 14.7 milliseconds Alpha Decay 93.00% Proton Emission 7.00% 162 107 milliseconds Alpha Decay 94.00% Electron Capture 6.00%

438

It's Elemental - Isotopes of the Element Francium  

NLE Websites -- All DOE Office Websites (Extended Search)

Radon Radon Previous Element (Radon) The Periodic Table of Elements Next Element (Radium) Radium Isotopes of the Element Francium [Click for Main Data] Most of the isotope data on this site has been obtained from the National Nuclear Data Center. Please visit their site for more information. Naturally Occurring Isotopes Francium has no naturally occurring isotopes. Known Isotopes Mass Number Half-life Decay Mode Branching Percentage 199 12 milliseconds Alpha Decay > 0.00% Electron Capture No Data Available 200 49 milliseconds Alpha Decay 100.00% 201 62 milliseconds Alpha Decay 100.00% 201m 19 milliseconds Alpha Decay 100.00% 202 0.30 seconds Alpha Decay 100.00% 202m 0.29 seconds Alpha Decay 100.00% 203 0.55 seconds Alpha Decay <= 100.00% 204 1.8 seconds Alpha Decay 92.00%

439

Building Energy Software Tools Directory: TRACE 700  

NLE Websites -- All DOE Office Websites (Extended Search)

700 700 TRACE 700 logo. Trane's TRACE 700 software - the latest version of Trane Air Conditioning Economics - brings the algorithms recommended by the American Society of Heating, Refrigerating, and Air-Conditioning Engineers (ASHRAE) to the familiar Windows operating environment. Use it to assess the energy and economic impacts of building-related selections such as architectural features, comfort-system design, HVAC equipment selections, operating schedules, and financial options. Flexible data entry, coupled with multiple views and "drag-and-drop" load assignments, simplify the modeling process and help you identify optimal zoning and plant configurations. Compare up to four alternatives for a single project by modeling various air distribution and mechanical

440

NEUTRONIC REACTOR CONTROL ELEMENT  

DOE Patents (OSTI)

A boron-10 containing reactor control element wherein the boron-10 is dispersed in a matrix material is describeri. The concentration of boron-10 in the matrix varies transversely across the element from a minimum at the surface to a maximum at the center of the element, prior to exposure to neutrons. (AEC)

Beaver, R.J.; Leitten, C.F. Jr.

1962-04-17T23:59:59.000Z

Note: This page contains sample records for the topic "trace elements 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.


441

Population, Economy and Energy Uses Influence on Sulfur Emissions in the United States Since 1900  

E-Print Network (OSTI)

This paper seeks to identify how changes in population, economic activity, and energy use have influenced sulfur emissions during this century. A linear model is presented which characterizes sulfur emissions as the product of these driving forces. The change in sulfur emissions is formulated as a function of changes in these trends. During this century, population growth and increasing economic activity have put upward pressure on sulfur emissions. The declining energy intensity of the economy and the transition from coal to less sulfur intensive fuels have reduced sulfur emissions. The net effect of all drivers has been moderate growth in sulfur emissions from 1900 to present. Since 1973, increased energy efficiency and the shift from an industrial to a commercially oriented economy have lowered the energy intensity of the economy. The increased use of low sulfur coal and reduced sulfur emissions from metal smelters have lowered the sulfur intensity of energy. These factors have combined to cause sulfur emissions to decline by 25%.

Kissock, J. K.

1990-06-01T23:59:59.000Z

442

Title Offline Trace Synchronization for Smartphone Energy Profiling  

E-Print Network (OSTI)

Energy profiling is a means to effectively understand the power behavior of smartphone applications. However, no tool that effectively combines portability, accuracy and automation has been proposed yet. In this thesis a new approach is proposed, which sets the basis for such a tool by solving a trace synchronization problem. TRAM (TRAce Merger) uses the event trace from a mobile device and the power trace from a measurement device. It synchronizes them offline, maps the mobile device events trace on the corresponding trace from the power measurement tool, and attributes energy consumption to smartphone functionalities. The event and power traces traces from these two systems contain timestamps based on the corresponding local clocks. Taking the aforementioned clocks inaccuracy and deviation into account, we synchronize these traces to extract useful information from their contents. We achieved energy consumption attribution to smartphone functionalities by solving this synchronization problem with milliseconds accuracy.

Ioannis Oikonomidis; Offline Trace; Synchronization Smartphone; Ioannis Oikonomidis; Msc Presentation

2013-01-01T23:59:59.000Z

443

Sulfur tolerant anode materials. Quarterly report, January 1--March 31, 1988  

DOE Green Energy (OSTI)

The goal of this program is the development of a molten carbonate fuel cell (MCFC) anode which is more tolerant of sulfur contaminants in the fuel than the current state-of-the-art nickel-based anode structures. This program addresses two different but related aspects of the sulfur contamination problem. The primary aspect is concerned with the development of a sulfur tolerant electrocatalyst for the fuel oxidation reaction. A secondary issue is the development of a sulfur tolerant water-gas-shift reaction catalyst and an investigation of potential steam reforming catalysts which also have some sulfur tolerant capabilities. These two aspects are being addressed as two separate tasks.

Not Available

1988-05-01T23:59:59.000Z

444

Method of burning sulfur-containing fuels in a fluidized bed boiler  

DOE Patents (OSTI)

A method of burning a sulfur-containing fuel in a fluidized bed of sulfur oxide sorbent wherein the overall utilization of sulfur oxide sorbent is increased by comminuting the bed drain solids to a smaller average particle size, preferably on the order of 50 microns, and reinjecting the comminuted bed drain solids into the bed. In comminuting the bed drain solids, particles of spent sulfur sorbent contained therein are fractured thereby exposing unreacted sorbent surface. Upon reinjecting the comminuted bed drain solids into the bed, the newly-exposed unreacted sorbent surface is available for sulfur oxide sorption, thereby increasing overall sorbent utilization.

Jones, Brian C. (Windsor, CT)

1982-01-01T23:59:59.000Z

445

Spent fuel pool analysis using TRACE code  

SciTech Connect

The storage requirements of Spent Fuel Pools have been analyzed with the purpose to increase their rack capacities. In the past, the thermal limits have been mainly evaluated with conservative codes developed for this purpose, although some works can be found in which a best estimate code is used. The use of best estimate codes is interesting as they provide more realistic calculations and they have the capability of analyzing a wide range of transients that could affect the Spent Fuel Pool. Two of the most representative thermal-hydraulic codes are RELAP-5 and TRAC. Nowadays, TRACE code is being developed to make use of the more favorable characteristics of RELAP-5 and TRAC codes. Among the components coded in TRACE that can be used to construct the model, it is interesting to use the VESSEL component, which has the capacity of reproducing three dimensional phenomena. In this work, a thermal-hydraulic model of the Maine Yankee spent fuel pool using the TRACE code is developed. Such model has been used to perform a licensing calculation and the results obtained have been compared with experimental measurements made at the pool, showing a good agreement between the calculations predicted by TRACE and the experimental data. (authors)

Sanchez-Saez, F.; Carlos, S.; Villanueva, J. F.; Martorell, S. [Dept. of Chemical and Nuclear Engineering, Universitat Politenica de Valencia, Cami de Vera s/n, 46021, Valencia (Spain)

2012-07-01T23:59:59.000Z

446

Stochastic path tracing on consumer graphics cards  

Science Conference Proceedings (OSTI)

We present a path tracer using the GPU of a consumers graphics card to render images. It is implemented in Java and GLSL using GroIMP as modelling platform and runtime environment. The path tracer is capable of rendering primitives like sphere, cone, ... Keywords: GPU, HDR, global illumination, path tracing, procedural texturing, raytracing, texture mapping

Thomas Huwe; Reinhard Hemmerling

2008-04-01T23:59:59.000Z