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1

Strategies for the Engineered Phytoremediation of Mercury and Arsenic Pollution  

Science Conference Proceedings (OSTI)

Phytoremediation is the use of plants to extract, transport, detoxify and/or sequester pollutants of the land, water or air. Mercury and arsenic are among the worst environmental pollutants, adversely affecting the health of hundreds of millions of people worldwide. We have demonstrated that plants can be engineered to take up and tolerate several times the levels of mercury and arsenic that would kill most plant species. Starting with methylmercury and/or ionic mercury contamination, mercury is detoxified, stored below or above ground, and even volatilized as part of the transpiration process and keeping it out of the food chain. Initial efforts with arsenate demonstrate that it can be taken up, transported aboveground, electrochemically reduced to arsenite in leaves and sequestered in thiol-rich peptide complexes. The transgenic mercury remediation strategies also worked in cultivated and wild plant species like canola, rice and cottonwood.

Dhankher, Om Parkash; Meagher, Richard B.

2003-03-26T23:59:59.000Z

2

The Hydrothermal Chemistry of Gold, Arsenic, Antimony, Mercury and Silver  

DOE Green Energy (OSTI)

A comprehensive thermodynamic database based on the Helgeson-Kirkham-Flowers (HKF) equation of state was developed for metal complexes in hydrothermal systems. Because this equation of state has been shown to accurately predict standard partial molal thermodynamic properties of aqueous species at elevated temperatures and pressures, this study provides the necessary foundation for future exploration into transport and depositional processes in polymetallic ore deposits. The HKF equation of state parameters for gold, arsenic, antimony, mercury, and silver sulfide and hydroxide complexes were derived from experimental equilibrium constants using nonlinear regression calculations. In order to ensure that the resulting parameters were internally consistent, those experiments utilizing incompatible thermodynamic data were re-speciated prior to regression. Because new experimental studies were used to revise the HKF parameters for H2S0 and HS-1, those metal complexes for which HKF parameters had been previously derived were also updated. It was found that predicted thermodynamic properties of metal complexes are consistent with linear correlations between standard partial molal thermodynamic properties. This result allowed assessment of several complexes for which experimental data necessary to perform regression calculations was limited. Oxygen fugacity-temperature diagrams were calculated to illustrate how thermodynamic data improves our understanding of depositional processes. Predicted thermodynamic properties were used to investigate metal transport in Carlin-type gold deposits. Assuming a linear relationship between temperature and pressure, metals are predicted to predominantly be transported as sulfide complexes at a total aqueous sulfur concentration of 0.05 m. Also, the presence of arsenic and antimony mineral phases in the deposits are shown to restrict mineralization within a limited range of chemical conditions. Finally, at a lesser aqueous sulfur concentration of 0.01 m, host rock sulfidation can explain the origin of arsenic and antimony minerals within the paragenetic sequence.

Bessinger, Brad; Apps, John A.

2003-03-23T23:59:59.000Z

3

Surface characterizatin of palladium-alumina sorbents for high-temperature capture of mercury and arsenic from fuel gas  

SciTech Connect

Coal gasification with subsequent cleanup of the resulting fuel gas is a way to reduce the impact of mercury and arsenic in the environment during power generation and on downstream catalytic processes in chemical production, The interactions of mercury and arsenic with PdlAl2D3 model thin film sorbents and PdlAh03 powders have been studied to determine the relative affinities of palladium for mercury and arsenic, and how they are affected by temperature and the presence of hydrogen sulfide in the fuel gas. The implications of the results on strategies for capturing the toxic metals using a sorbent bed are discussed.

Baltrus, J.P.; Granite, E.J.; Pennline, H.W.; Stanko, D.; Hamilton, H.; Rowsell, L.; Poulston, S.; Smith, A.; Chu, W.

2010-01-01T23:59:59.000Z

4

Screening of low cost sorbents for arsenic and mercury capture in gasification systems  

Science Conference Proceedings (OSTI)

A novel laboratory-scale fixed-bed reactor has been developed to investigate trace metal capture on selected sorbents for cleaning the hot raw gas in Integrated Gasification Combined Cycle (IGCC) power plants. The new reactor design is presented, together with initial results for mercury and arsenic capture on five sorbents. It was expected that the capture efficiency of sorbents would decrease with increasing temperature. However, a commercial activated carbon, Norit Darco 'Hg', and a pyrolysis char prepared from scrap tire rubber exhibit similar efficiencies for arsenic at 200 and at 400{sup o}C (70% and 50%, respectively). Meta-kaolinite and fly ash both exhibit an efficiency of around 50% at 200{sup o}C, which then dropped as the test temperature was increased to 400{sup o}C. Activated scrap tire char performed better at 200{sup o}C than the pyrolysis char showing an arsenic capture capacity similar to that of commercial Norit Darco 'Hg'; however, efficiency dropped to below 40% at 400{sup o}C. These results suggest that the capture mechanism of arsenic (As4) is more complex than purely physical adsorption onto the sorbents. Certain elements within the sorbents may have significant importance for chemical adsorption, in addition to the effect of surface area, as determined by the BET method. This was indeed the case for the mercury capture efficiency for all four sorbents tested. Three of the sorbents tested retained 90% of the mercury when operated at 100{sup o}C. As the temperature increased, the efficiency of activated carbon and pyrolysis char reduced significantly. Curiously, despite having the smallest Brunauer-Emmet-Teller (BET) surface area, a pf-combustion ash was the most effective in capturing mercury over the temperature range studied. These observations suggest that the observed mercury capture was not purely physical adsorption but a combination of physical and chemical processes. 27 refs., 4 figs., 4 tabs.

Cedric Charpenteau; Revata Seneviratne; Anthe George; Marcos Millan; Denis R. Dugwell; Rafael Kandiyoti [Imperial College London, London (United Kingdom). Department of Chemical Engineering

2007-09-15T23:59:59.000Z

5

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

Science Conference Proceedings (OSTI)

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

Ye Zhuang; Christopher Martin; John Pavlish

2009-03-31T23:59:59.000Z

6

Sorption of Arsenic, Mercury, Selenium onto Nanostructured Adsorbent Media and Stabilization via Surface Reactions  

E-Print Network (OSTI)

The overall goal of this study is to evaluate the ability of novel nanostructured adsorbent media (NTAs, iron sulfides (FeS2 and FeS)) to remove arsenic, selenium and mercury from ash and scrubber pond effluents. The NTAs aim to enhance arsenic removal from solution compared to conventional adsorbents. The iron sulfides are expected to produce stable residuals for ultimate disposal after removing As, Se and Hg from solution, so that removal of these compounds from wastewaters will not result in contamination of soils and groundwaters. Methods for reliably and economically producing these materials were developed. The synthesized NTAs and iron sulfides were characterized by surface analysis techniques such as XRD, FT-IR, SEM-EDS, TEM, XPS, AFM and N2-adsorption. These analyses indicated that Ti(25)-SBA-15 has highly ordered hexagonal mesopores, MT has interparticle mesopores, pyrite (FeS2) forms crystalline, nonporous rectangular nanoparticles (<500 nm), and mackinawite (FeS) forms amorphous, nonporous nanoparticles (<100 nm). Kinetic and equilibrium tests for As(III, V) removal were conducted with NTAs over a range of pH (4, 7, 9.5). The rates of arsenic uptake were very fast and followed a bi-phasic sorption pattern, where sorption was fast for the first 10 minutes, and then slowed and was almost completed within 200 minutes. Distinct sorption maxima for As(III) removal were observed between pH 7 and pH 9.5 for MT and between pH 4 and pH 7 for Ti(25)-SBA-15. The amount of As(V) adsorbed generally decreased as pH increased. In addition, a surface complexation model (SCM) based on the diffuse layer model (DLM) was used to predict arsenic adsorption envelopes by NTAs under various environmental conditions. The SCM for As(III, V) adsorption by NTAs demonstrated the role of mono- and bidentate surface complexes in arsenic adsorption. A batch reactor system was employed in an anaerobic chamber to conduct experiments to characterize both the removal of As, Se, Hg from solution and their subsequent reactions with iron sulfides. Experiment variables for removal experiments included: contaminant valence state (As(V), As(III), Se(VI), Se(IV), Hg(II)); adsorbent/reactant type (FeS, FeS2); adsorbent/reactant concentration; pH (7, 8, 9, 10); and competing ion (SO42-) concentration (0, 1, 10 mM). Experimental variables for reaction experiments were reaction time (up to 30 days) at pH 8 and oxidation states of contaminants. In addition, the stability of iron sulfides (FeS2, FeS) combined with target compounds was investigated by measuring the ability of the target compounds to resist release to the aqueous phase after removal. These experiments showed that iron sulfides were good adsorbent/reactants for target contaminants in spite of the presence of sulfate. This was particularly true at intermediate concentrations of target compounds. The experiments also demonstrated that iron sulfides interacted with target contaminants in such a way to improve their resistance to being released back to solution as pH was changed. Therefore, this study demonstrates the ability of novel nanostructured adsorbent media to remove arsenic, selenium and mercury from ash and scrubber pond effluents and the ability of iron sulfides to produce residuals that are stable when disposed in landfills.

Han, Dong Suk

2009-12-01T23:59:59.000Z

7

EVALUATION OF THE EMISSION, TRANSPORT, AND DEPOSITION OF MERCURY, FINE PARTICULATE MATTER, AND ARSENIC FROM COAL-BASED POWER PLANTS IN THE OHIO RIVER VALLEY REGION  

Science Conference Proceedings (OSTI)

Ohio University, in collaboration with CONSOL Energy, Advanced Technology Systems, Inc (ATS) and Atmospheric and Environmental Research, Inc. (AER) as subcontractors, is evaluating the impact of emissions from coal-fired power plants in the Ohio River Valley region as they relate to the transport and deposition of mercury, arsenic, and associated fine particulate matter. This evaluation will involve two interrelated areas of effort: ambient air monitoring and regional-scale modeling analysis. The scope of work for the ambient air monitoring will include the deployment of a surface air monitoring (SAM) station in southeastern Ohio. The SAM station will contain sampling equipment to collect and measure mercury (including speciated forms of mercury and wet and dry deposited mercury), arsenic, particulate matter (PM) mass, PM composition, and gaseous criteria pollutants (CO, NO{sub x}, SO{sub 2}, O{sub 3}, etc.). Laboratory analysis of time-integrated samples will be used to obtain chemical speciation of ambient PM composition and mercury in precipitation. Near-real-time measurements will be used to measure the ambient concentrations of PM mass and all gaseous species including Hg{sup 0} and RGM. Approximately of 18 months of field data will be collected at the SAM site to validate the proposed regional model simulations for episodic and seasonal model runs. The ambient air quality data will also provide mercury, arsenic, and fine particulate matter data that can be used by Ohio Valley industries to assess performance on multi-pollutant control systems. The scope of work for the modeling analysis will include (1) development of updated inventories of mercury and arsenic emissions from coal plants and other important sources in the modeled domain; (2) adapting an existing 3-D atmospheric chemical transport model to incorporate recent advancements in the understanding of mercury transformations in the atmosphere; (3) analyses of the flux of Hg{sup 0}, RGM, arsenic, and fine particulate matter in the different sectors of the study region to identify key transport mechanisms; (4) comparison of cross correlations between species from the model results to observations in order to evaluate characteristics of specific air masses associated with long-range transport from a specified source region; and (5) evaluation of the sensitivity of these correlations to emissions from regions along the transport path. This will be accomplished by multiple model runs with emissions simulations switched on and off from the various source regions. To the greatest extent possible, model results will also be compared to field data collected at other air monitoring sites in the Ohio Valley Region, operated independently of this project. These sites may include (1) the DOE National Energy Technologies Laboratory's monitoring site at its suburban Pittsburgh, PA facility; (2) sites in Pittsburgh (Lawrenceville) PA and Holbrook, PA operated by ATS; (3) sites in Steubenville, OH and Pittsburgh, PA operated by U.S. EPA and/or its contractors; and (4) sites operated by State or local air regulatory agencies. Field verification of model results and predictions will provide critical information for the development of cost effective air pollution control strategies by the coal-fired power plants in the Ohio River Valley Region.

Kevin Crist

2003-10-02T23:59:59.000Z

8

EVALUATION OF THE EMISSION, TRANSPORT, AND DEPOSITION OF MERCURY, FINE PARTICULATE MATTER, AND ARSENIC FROM COAL-BASED POWER PLANTS IN THE OHIO RIVER VALLEY REGION  

Science Conference Proceedings (OSTI)

Ohio University, in collaboration with CONSOL Energy, Advanced Technology Systems, Inc (ATS) and Atmospheric and Environmental Research, Inc. (AER) as subcontractors, is evaluating the impact of emissions from coal-fired power plants in the Ohio River Valley region as they relate to the transport and deposition of mercury, arsenic, and associated fine particulate matter. This evaluation will involve two interrelated areas of effort: ambient air monitoring and regional-scale modeling analysis. The scope of work for the ambient air monitoring will include the deployment of a surface air monitoring (SAM) station in southeastern Ohio. The SAM station will contain sampling equipment to collect and measure mercury (including speciated forms of mercury and wet and dry deposited mercury), arsenic, particulate matter (PM) mass, PM composition, and gaseous criteria pollutants (CO, NO{sub x}, SO{sub 2}, O{sub 3}, etc.). Laboratory analysis of time-integrated samples will be used to obtain chemical speciation of ambient PM composition and mercury in precipitation. Near-real-time measurements will be used to measure the ambient concentrations of PM mass and all gaseous species including Hg{sup 0} and RGM. Approximately of 18 months of field data will be collected at the SAM site to validate the proposed regional model simulations for episodic and seasonal model runs. The ambient air quality data will also provide mercury, arsenic, and fine particulate matter data that can be used by Ohio Valley industries to assess performance on multi-pollutant control systems. The scope of work for the modeling analysis will include (1) development of updated inventories of mercury and arsenic emissions from coal plants and other important sources in the modeled domain; (2) adapting an existing 3-D atmospheric chemical transport model to incorporate recent advancements in the understanding of mercury transformations in the atmosphere; (3) analyses of the flux of Hg{sup 0}, RGM, arsenic, and fine particulate matter in the different sectors of the study region to identify key transport mechanisms; (4) comparison of cross correlations between species from the model results to observations in order to evaluate characteristics of specific air masses associated with long-range transport from a specified source region; and (5) evaluation of the sensitivity of these correlations to emissions from regions along the transport path. This will be accomplished by multiple model runs with emissions simulations switched on and off from the various source regions. To the greatest extent possible, model results will also be compared to field data collected at other air monitoring sites in the Ohio Valley region, operated independently of this project. These sites may include (1) the DOE National Energy Technologies Laboratory's monitoring site at its suburban Pittsburgh, PA facility; (2) sites in Pittsburgh (Lawrenceville) PA and Holbrook, PA operated by ATS; (3) sites in Steubenville, OH and Pittsburgh, PA operated by U.S. EPA and/or its contractors; and (4) sites operated by State or local air regulatory agencies. Field verification of model results and predictions will provide critical information for the development of cost effective air pollution control strategies by the coal-fired power plants in the Ohio River Valley region.

Kevin Crist

2005-04-02T23:59:59.000Z

9

EVALUATION OF THE EMISSION, TRANSPORT, AND DEPOSITION OF MERCURY, FINE PARTICULATE MATTER, AND ARSENIC FROM COAL-BASED POWER PLANTS IN THE OHIO RIVER VALLEY REGION  

Science Conference Proceedings (OSTI)

Ohio University, in collaboration with CONSOL Energy, Advanced Technology Systems, Inc (ATS) and Atmospheric and Environmental Research, Inc. (AER) as subcontractors, is evaluating the impact of emissions from coal-fired power plants in the Ohio River Valley region as they relate to the transport and deposition of mercury, arsenic, and associated fine particulate matter. This evaluation will involve two interrelated areas of effort: ambient air monitoring and regional-scale modeling analysis. The scope of work for the ambient air monitoring will include the deployment of a surface air monitoring (SAM) station in southeastern Ohio. The SAM station will contain sampling equipment to collect and measure mercury (including speciated forms of mercury and wet and dry deposited mercury), arsenic, particulate matter (PM) mass, PM composition, and gaseous criteria pollutants (CO, NOx, SO{sub 2}, O{sub 3}, etc.). Laboratory analysis of time-integrated samples will be used to obtain chemical speciation of ambient PM composition and mercury in precipitation. Near-real-time measurements will be used to measure the ambient concentrations of PM mass and all gaseous species including Hg{sup 0} and RGM. Approximately of 18 months of field data will be collected at the SAM site to validate the proposed regional model simulations for episodic and seasonal model runs. The ambient air quality data will also provide mercury, arsenic, and fine particulate matter data that can be used by Ohio Valley industries to assess performance on multi-pollutant control systems. The scope of work for the modeling analysis will include (1) development of updated inventories of mercury and arsenic emissions from coal plants and other important sources in the modeled domain; (2) adapting an existing 3-D atmospheric chemical transport model to incorporate recent advancements in the understanding of mercury transformations in the atmosphere; (3) analyses of the flux of Hg{sup 0}, RGM, arsenic, and fine particulate matter in the different sectors of the study region to identify key transport mechanisms; (4) comparison of cross correlations between species from the model results to observations in order to evaluate characteristics of specific air masses associated with long-range transport from a specified source region; and (5) evaluation of the sensitivity of these correlations to emissions from regions along the transport path. This will be accomplished by multiple model runs with emissions simulations switched on and off from the various source regions. To the greatest extent possible, model results will also be compared to field data collected at other air monitoring sites in the Ohio Valley region, operated independently of this project. These sites may include (1) the DOE National Energy Technologies Laboratory's monitoring site at its suburban Pittsburgh, PA facility; (2) sites in Pittsburgh (Lawrenceville) PA and Holbrook, PA operated by ATS; (3) sites in Steubenville, OH and Pittsburgh, PA operated by U.S. EPA and/or its contractors; and (4) sites operated by State or local air regulatory agencies. Field verification of model results and predictions will provide critical information for the development of cost effective air pollution control strategies by the coal-fired power plants in the Ohio River Valley region.

Kevin Crist

2004-10-02T23:59:59.000Z

10

Evaluation of the Emission, Transport, and Deposition of Mercury, Fine Particulate Matter, and Arsenic from Coal-Based Power Plants in the Ohio River Valley Region  

Science Conference Proceedings (OSTI)

Ohio University, in collaboration with CONSOL Energy, Advanced Technology Systems, Inc (ATS) and Atmospheric and Environmental Research, Inc. (AER) as subcontractors, is evaluating the impact of emissions from coal-fired power plants in the Ohio River Valley region as they relate to the transport and deposition of mercury, arsenic, and associated fine particulate matter. This evaluation will involve two interrelated areas of effort: ambient air monitoring and regional-scale modeling analysis. The scope of work for the ambient air monitoring will include the deployment of a surface air monitoring (SAM) station in southeastern Ohio. The SAM station will contain sampling equipment to collect and measure mercury (including speciated forms of mercury and wet and dry deposited mercury), arsenic, particulate matter (PM) mass, PM composition, and gaseous criteria pollutants (CO, NOx, SO{sub 2}, O{sub 3}, etc.). Laboratory analysis of time-integrated samples will be used to obtain chemical speciation of ambient PM composition and mercury in precipitation. Near-real-time measurements will be used to measure the ambient concentrations of PM mass and all gaseous species including Hg{sup 0} and RGM. Approximately of 18 months of field data will be collected at the SAM site to validate the proposed regional model simulations for episodic and seasonal model runs. The ambient air quality data will also provide mercury, arsenic, and fine particulate matter data that can be used by Ohio Valley industries to assess performance on multi-pollutant control systems. The scope of work for the modeling analysis will include (1) development of updated inventories of mercury and arsenic emissions from coal plants and other important sources in the modeled domain; (2) adapting an existing 3-D atmospheric chemical transport model to incorporate recent advancements in the understanding of mercury transformations in the atmosphere; (3) analyses of the flux of Hg0, RGM, arsenic, and fine particulate matter in the different sectors of the study region to identify key transport mechanisms; (4) comparison of cross correlations between species from the model results to observations in order to evaluate characteristics of specific air masses associated with long-range transport from a specified source region; and (5) evaluation of the sensitivity of these correlations to emissions from regions along the transport path. This will be accomplished by multiple model runs with emissions simulations switched on and off from the various source regions. To the greatest extent possible, model results will also be compared to field data collected at other air monitoring sites in the Ohio Valley region, operated independently of this project. These sites may include (1) the DOE National Energy Technologies Laboratory's monitoring site at its suburban Pittsburgh, PA facility; (2) sites in Pittsburgh (Lawrenceville) PA and Holbrook, PA operated by ATS; (3) sites in Steubenville, OH and Pittsburgh, PA operated by U.S. EPA and/or its contractors; and (4) sites operated by State or local air regulatory agencies. Field verification of model results and predictions will provide critical information for the development of cost effective air pollution control strategies by the coal-fired power plants in the Ohio River Valley region.

Kevin Crist

2005-10-02T23:59:59.000Z

11

EVALUATION OF THE EMISSION, TRANSPORT, AND DEPOSITION OF MERCURY, FINE PARTICULATE MATTER, AND ARSENIC FROM COAL-BASED POWER PLANTS IN THE OHIO RIVER VALLEY REGION  

Science Conference Proceedings (OSTI)

Ohio University, in collaboration with CONSOL Energy, Advanced Technology Systems, Inc. (ATS) and Atmospheric and Environmental Research, Inc. (AER) as subcontractors, is evaluating the impact of emissions from coal-fired power plants in the Ohio River Valley region as they relate to the transport and deposition of mercury, arsenic, and associated fine particulate matter. This evaluation will involve two interrelated areas of effort: ambient air monitoring and regional-scale modeling analysis. The scope of work for the ambient air monitoring will include the deployment of a surface air monitoring (SAM) station in southeastern Ohio. The SAM station will contain sampling equipment to collect and measure mercury (including speciated forms of mercury and wet and dry deposited mercury), arsenic, particulate matter (PM) mass, PM composition, and gaseous criteria pollutants (CO, NOx, SO{sub 2}, O{sub 3}, etc.). Laboratory analysis of time-integrated samples will be used to obtain chemical speciation of ambient PM composition and mercury in precipitation. Near-real-time measurements will be used to measure the ambient concentrations of PM mass and all gaseous species including Hg{sup 0} and RGM. Approximately 18 months of field data will be collected at the SAM site to validate the proposed regional model simulations for episodic and seasonal model runs. The ambient air quality data will also provide mercury, arsenic, and fine particulate matter data that can be used by Ohio Valley industries to assess performance on multi-pollutant control systems. The scope of work for the modeling analysis will include (1) development of updated inventories of mercury and arsenic emissions from coal-fired power plants and other important sources in the modeled domain; (2) adapting an existing 3-D atmospheric chemical transport model to incorporate recent advancements in the understanding of mercury transformations in the atmosphere; (3) analyses of the flux of Hg{sup 0}, RGM, arsenic, and fine particulate matter in the different sectors of the study region to identify key transport mechanisms; (4) comparison of cross correlations between species from the model results to observations in order to evaluate characteristics of specific air masses associated with long-range transport from a specified source region; and (5) evaluation of the sensitivity of these correlations to emissions from regions along the transport path. This will be accomplished by multiple model runs with emissions simulations switched on and off from the various source regions. To the greatest extent possible, model results will also be compared to field data collected at other air monitoring sites in the Ohio Valley Region, operated independently of this project. These sites may include (1) the DOE National Energy Technology Laboratory's monitoring site at its suburban Pittsburgh, PA facility; (2) sites in Pittsburgh (Lawrenceville) PA and Holbrook, PA operated by ATS; (3) sites in Steubenville, OH and Pittsburgh, PA operated by U.S. EPA and/or its contractors; and (4) sites operated by State or local air regulatory agencies. Field verification of model results and predictions will provide critical information for the development of cost effective air pollution control strategies by the coal-fired power plants in the Ohio River Valley region.

Kevin Crist

2004-04-02T23:59:59.000Z

12

Evaluation of the Emission, Transport, and Deposition of Mercury, Fine Particulate Matter, and Arsenic from Coal-Based Power Plants in the Ohio River Valley Region  

Science Conference Proceedings (OSTI)

As stated in the proposal: Ohio University, in collaboration with CONSOL Energy, Advanced Technology Systems, Inc (ATS) and Atmospheric and Environmental Research, Inc. (AER) as subcontractors, is evaluating the impact of emissions from coal-fired power plants in the Ohio River Valley region as they relate to the transport and deposition of mercury, arsenic, and associated fine particulate matter. This evaluation will involve two interrelated areas of effort: ambient air monitoring and regional-scale modeling analysis. The scope of work for the ambient air monitoring will include the deployment of a surface air monitoring (SAM) station in southeastern Ohio. The SAM station will contain sampling equipment to collect and measure mercury (including speciated forms of mercury and wet and dry deposited mercury), arsenic, particulate matter (PM) mass, PM composition, and gaseous criteria pollutants (CO, NO{sub x}, SO{sub 2}, O{sub 3}, etc.). Laboratory analysis of time-integrated samples will be used to obtain chemical speciation of ambient PM composition and mercury in precipitation. Near-real-time measurements will be used to measure the ambient concentrations of PM mass and all gaseous species including Hg0 and RGM. Approximately 18 months of field data will be collected at the SAM site to validate the proposed regional model simulations for episodic and seasonal model runs. The ambient air quality data will also provide mercury, arsenic, and fine particulate matter data that can be used by Ohio Valley industries to assess performance on multi-pollutant control systems. The scope of work for the modeling analysis will include (1) development of updated inventories of mercury and arsenic emissions from coal plants and other important sources in the modeled domain; (2) adapting an existing 3-D atmospheric chemical transport model to incorporate recent advancements in the understanding of mercury transformations in the atmosphere; (3) analyses of the flux of Hg{sup 0}, RGM, arsenic, and fine particulate matter in the different sectors of the study region to identify key transport mechanisms; (4) comparison of cross correlations between species from the model results to observations in order to evaluate characteristics of specific air masses associated with long-range transport from a specified source region; and (5) evaluation of the sensitivity of these correlations to emissions from regions along the transport path. This will be accomplished by multiple model runs with emissions simulations switched on and off from the various source regions. To the greatest extent possible, model results will also be compared to field data collected at other air monitoring sites in the Ohio Valley region, operated independently of this project. These sites may include (1) the DOE National Energy Technologies Laboratory's monitoring site at its suburban Pittsburgh, PA facility; (2) sites in Pittsburgh (Lawrenceville) PA and Holbrook, PA operated by ATS; (3) sites in Steubenville, OH and Pittsburgh, PA operated by the USEPA and/or its contractors; and (4) sites operated by State or local air regulatory agencies. Field verification of model results and predictions will provide critical information for the development of cost effective air pollution control strategies by the coal-fired power plants in the Ohio River Valley region.

Kevin Crist

2006-04-02T23:59:59.000Z

13

Evaluation of the Emission, Transport, and Deposition of Mercury, Arsenic, and Fine Particulate Matter From Coal-Based Power Plants in the Ohio River Valley  

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

Kevin crist Kevin crist Principal Investigator Ohio University Research and Technology Center Athens, OH 45701 740-593-4751 cristk@ohiou.edu Environmental and Water Resources Evaluation of thE Emission, transport, and dEposition of mErcury, arsEnic, and finE particulatE mattEr from coal-BasEd powEr plants in thE ohio rivEr vallEy rEgion Background The U.S. Department of Energy's National Energy Technology Laboratory (NETL) has established an aggressive research initiative to address the technical and scientific issues surrounding the impact of coal-based power systems on ambient levels of fine particulate matter (PM 2.5 ), nitrogen oxides (NO X ), mercury/air toxics, and acid gases. Regulatory drivers such as the 1990 Clean Air Act Amendments, the 1997 revised National Ambient Air Quality Standards, and the 2005 Clean Air

14

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

SciTech Connect

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

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

2009-09-15T23:59:59.000Z

15

Drinking Water Problems: Arsenic  

E-Print Network (OSTI)

High levels of arsenic in drinking water can poison and even kill people. This publication explains the symptoms of arsenic poisoning and common treatment methods for removing arsenic from your water supply.

Lesikar, Bruce J.; Melton, Rebecca; Hare, Michael; Hopkins, Janie; Dozier, Monty

2005-12-02T23:59:59.000Z

16

Radionuclide trap  

DOE Patents (OSTI)

The deposition of radionuclides manganese-54, cobalt-58 and cobalt-60 from liquid sodium coolant is controlled by providing surfaces of nickel or high nickel alloys to extract the radionuclides from the liquid sodium, and by providing surfaces of tungsten, molybdenum or tantalum to prevent or retard radionuclide deposition.

McGuire, Joseph C. (Richland, WA)

1978-01-01T23:59:59.000Z

17

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

18

Arsenic Health Research Synthesis  

Science Conference Proceedings (OSTI)

This report summarizes EPRI-sponsored arsenic health research results to date, examines implications of these results for reducing uncertainties in arsenic cancer risk assessment, and identifies remaining research needs. The most important contributions of this research toward reducing key uncertainties for arsenic cancer risk estimates include a revised arsenic inhalation unit risk value, support for a nonlinear dose-response relationship, an estimate of bioavailability of arsenic in coal fly ash, deter...

2001-06-12T23:59:59.000Z

19

Publications | Mercury  

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

A. Afsahi, and R. Ross, Mercury: Enabling Remote Procedure Call for High-Performance Computing, IEEE International Conference on Cluster Computing, Sep 2013. DOIslides...

20

2010 EPRI-Southern Company Services Activated Carbon Mercury Control Workshop Proceedings  

Science Conference Proceedings (OSTI)

The U.S. Environmental Protection Agency (EPA) proposed a maximum achievable control technology ruling for air toxics on March 16, 2011. The proposed rule would impose new emission limits on mercury, acid gases, and particulate matter (as a surrogate for non-mercury metallic pollutants such as arsenic) from coal-fired power plants. These new limits are in addition to already existing mercury emissions limits imposed by many states. Activated carbon injection (ACI) is one of the leading control options to...

2011-04-28T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

NETL: Utilization Projects - Speciation and Attenuation of Arsenic and  

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

Speciation and Attenuation of Arsenic and Selenium at Coal Combustion By-Product Management Facilities Speciation and Attenuation of Arsenic and Selenium at Coal Combustion By-Product Management Facilities The overall objective of this project is to evaluate the impact of key constituents captured from power plant air streams (arsenic, selenium and mercury) on the disposal and utilization of coal combustion by-products. Specific objectives of the project are: 1) to develop a comprehensive database of field leachate concentrations at a wide range of CCB management sites (about 25 sites), including speciation of arsenic and selenium, and low-detection limit analyses for mercury; and 2) to perform detailed evaluations of the release and attenuation of arsenic and selenium species at 3 CCB sites. The fundamental or mechanistic data to reliably model many of the inorganics in CCB leachate are lacking. There is a large degree of uncertainty in the initial leachate concentrations, long-term leaching characteristics of CCBs, and the attenuation coefficients typically used in groundwater transport models. As a result, the model simulations are either highly conservative, or they can be manipulated to obtain almost any desired result. This research project will develop a coherent field leachate database and soil attenuation coefficients for improved modeling and evaluation of the potential for groundwater impacts at CCB management facilities. The work is focused on speciation of four key constituents at CCB sites: arsenic, selenium, chromium, and mercury. The proposed work will help to narrow the uncertainties in the range of values of these critical inputs and improve the accuracy of the modeling results.

22

Mercury Vapor Pressure Correlation  

Science Conference Proceedings (OSTI)

An apparent difference between the historical mercury vapor concentration equations used by the mercury atmospheric measurement community ...

2012-10-09T23:59:59.000Z

23

Arsenic Health Research Update  

Science Conference Proceedings (OSTI)

The Electric Power Research Institute (EPRI) research program investigating the health effects of inorganic arsenic continues to focus on understanding the biological significance of low-level inorganic arsenic exposure. The major component of ongoing work is the development of an alternative, nonlinear approach to revising the inorganic arsenic cancer potency value (or cancer slope factor). Current, default linear approaches for establishing a cancer slope factor do not account for the biological mode o...

2010-12-31T23:59:59.000Z

24

Arsenic activation neutron detector  

DOE Patents (OSTI)

A detector of bursts of neutrons from a deuterium-deuteron reaction includes a quantity of arsenic adjacent a gamma detector such as a scintillator and photomultiplier tube. The arsenic is activated by the 2.5-MeV neutrons to release gamma radiation which is detected to give a quantitative representation of detected neutrons.

Jacobs, E.L.

1980-01-28T23:59:59.000Z

25

Glossary Term - Mercury  

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

Liquid Nitrogen Previous Term (Liquid Nitrogen) Glossary Main Index Next Term (Mole) Mole Mercury Mercury as seen by the Mariner 10 spacecraft on March 24, 1974. Mercury is the...

26

Mercury-selenium interactions in the environment  

Science Conference Proceedings (OSTI)

The Clean Air Act Amendments of 1990 require the U.S. Environmental Protection Agency (EPA) to consider the need to control emissions of trace elements and compounds emitted from coal combustion, including coal-fired power plants. Concern has been expressed about emissions of mercury and arsenic, for example, since health effects may be associated with exposure to some of these compounds. By and large, effects of trace element emissions have been considered individually, without regard for possible interactions. To the extent that the relevant environmental pathways and health endpoints differ, this mode of analysis is appropriate. For example, arsenic is considered a carcinogen and mercury affects the brain. However, there may be compelling reasons to consider emissions of mercury (Hg) and selenium (Se) together: (1) Both Se and Hg are emitted from power plants primarily as vapors. (2) Hg and Se are both found in fish, which is the primary pathway for Hg health effects. (3) Se has been shown to suppress Hg methylation in aqueous systems, which is a necessary step for Hg health effects at current environmental concentrations. (4) Se is a trace element that is essential for health but that can also be toxic at high concentrations; it can thus have both beneficial and adverse health effects, depending on the dosage. This paper reviews some of the salient characteristics and interactions of the Hg-Se system, to consider the hypothesis that the effects of emissions of these compounds should be considered jointly.

Saroff, L. [Department of Energy, Washington, DC (United States); Lipfert, W.; Moskowitz, P.D. [Brookhaven National Lab., Upton, NY (United States). Dept. of Applied Science

1996-02-01T23:59:59.000Z

27

Phytoremediation of Ionic and Methyl Mercury P  

DOE Green Energy (OSTI)

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

Meagher, Richard B.

1999-06-01T23:59:59.000Z

28

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

29

Mercury contamination extraction  

DOE Patents (OSTI)

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

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

2009-09-15T23:59:59.000Z

30

Atomic Data for Mercury (Hg)  

Science Conference Proceedings (OSTI)

... Mercury (Hg) Homepage - Introduction Finding list Select element by name. Select element by atomic number. ... Atomic Data for Mercury (Hg). ...

31

Strong Lines of Mercury ( Hg )  

Science Conference Proceedings (OSTI)

... Mercury (Hg) Homepage - Introduction Finding list Select element by name. Select element by atomic number. ... Strong Lines of Mercury ( Hg ). ...

32

Radionuclide deposition control  

DOE Patents (OSTI)

The deposition of radionuclides manganese-54, cobalt-58 and cobalt-60 from liquid sodium coolant is controlled by providing surfaces of nickel or high nickel alloys to extract the radionuclides from the liquid sodium, and by providing surfaces of tungsten, molybdenum or tantalum to prevent or retard radionuclide deposition.

Brehm, William F. (Richland, WA); McGuire, Joseph C. (Richland, WA)

1980-01-01T23:59:59.000Z

33

Mercury and Fish  

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

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

34

NETL: IEP - Mercury and Air Toxic Element Impacts of CCB Disposal and  

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

Mercury and Air Toxic Element Impacts of CCB Disposal and Utilization Mercury and Air Toxic Element Impacts of CCB Disposal and Utilization The goal of the proposed effort is to evaluate the impact of mercury and other air toxic elements on the management of CCBs. Supporting objectives are to 1) determine the release potential of selected air toxic elements, including mercury and arsenic, from CCBs under specific environmental conditions; 2) increase the database of information on mercury and other air toxic element releases for CCBs; 3) develop comparative laboratory and field data; and 4) develop appropriate laboratory and field protocols. The specific mechanisms of air toxic element releases to be evaluated will be leaching releases, vapor releases to the atmosphere, and biologically induced leaching and vapor releases.

35

Mercury's Protoplanetary Mass  

E-Print Network (OSTI)

Major element fractionation among chondrites has been discussed for decades as ratios relative to Si or Mg. Recently, by expressing ratios relative to Fe, I discovered a new relationship admitting the possibility that ordinary chondrite meteorites are derived from two components, a relatively oxidized and undifferentiated, primitive component and a somewhat differentiated, planetary component, with oxidation state like the highly reduced enstatite chondrites, which I suggested was identical to Mercury's complement of lost elements. Here, on the basis of that relationship, I derive expressions, as a function of the mass of planet Mercury and the mass of its core, to estimate the mass of Mercury's lost elements, the mass of Mercury's alloy and rock protoplanetary core, and the mass of Mercury's gaseous protoplanet. Although Mercury's mass is well known, its core mass is not, being widely believed to be in the range of 70-80 percent of the planet mass. For a core mass of 75 percent, the mass of Mercury's lost elements is about 1.32 times the mass of Mercury, the mass of the alloy and rock protoplanetary core is about 2.32 times the mass of Mercury, and the mass of the gaseous protoplanet of Mercury is about 700 times the mass of Mercury. Circumstantial evidence is presented in support of the supposition that Mercury's lost elements is identical to the planetary component of ordinary chondrite formation.

J. Marvin Herndon

2004-10-01T23:59:59.000Z

36

Mercury in the Environment  

Science Conference Proceedings (OSTI)

EPRI periodically issues updates on critical research on environmental mercury, discussing scientific findings of crucial interest for a complete understanding of mercury sources, transport, fate, cycling, human exposure, and health effects. This document is part of that EPRI series, focusing on several critical reviews of mercury sources and impacts.

2007-03-30T23:59:59.000Z

37

Watershed Mercury Loading Framework  

Science Conference Proceedings (OSTI)

This report explains and illustrates a simplified stochastic framework, the Watershed Mercury Loading Framework, for organizing and framing site-specific knowledge and information on mercury loading to waterbodies. The framework permits explicit treatment of data uncertainties. This report will be useful to EPRI members, state and federal regulatory agencies, and watershed stakeholders concerned with mercury-related human and ecological health risk.

2003-05-23T23:59:59.000Z

38

Studies of Mercury in High Level Waste Systems  

Science Conference Proceedings (OSTI)

During nuclear weapons production, nuclear reactor target and fuel rods were processed in F- and H-Canyons. For the target rods, a caustic dissolution of the aluminum cladding was performed prior to nitric acid dissolution of the uranium metal targets in the large canyon dissolvers. To dissolve the aluminum cladding and the U-Al fuel, mercury in the form of soluble mercury (II) nitrate was added as a catalyst to accelerate the dissolution of the aluminum. F-Canyon began to process plutonium-containing residues that were packaged in aluminum cans and thus required the use of mercury as a dissolution catalyst. Following processing to remove uranium and plutonium using the solvent extraction process termed the Plutonium-Uranium Recovery by Extraction (PUREX) process, the acidic waste solutions containing fission products and other radionuclides were neutralized with sodium hydroxide. The mercury used in canyon processing is fractionated between the sludge and supernate that is transferred from the canyons to the tank farm. The sludge component of the waste is currently vitrified in the Defense Waste Processing Facility (DWPF). The vitrified waste canisters are to be sent to the federal repository for High Level Waste. The mercury in the sludge, presumably in an oxide or hydroxide form is reduced to elemental mercury by the chemical additions and high temperatures, steam stripped and collected in the Mercury Collection Tank. The mercury in the dilute supernate is in the form of mercuric ion and is soluble. During evaporation, the mercuric ion is reduced to elemental mercury, vaporizes into the overheads system and is collected as a metallic liquid in the Mercury Removal Tank.

Wilmarth, W.R.

2003-09-03T23:59:59.000Z

39

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

40

Radionuclides Applied to Tribology  

Science Conference Proceedings (OSTI)

...C.C. Blatchley, Radionuclide Methods, Friction, Lubrication, and Wear Technology, Vol 18, ASM Handbook, ASM International, 1992, p 319??329...

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Treatment of Wastes Containing Arsenic, Selenium and Mercury I  

Science Conference Proceedings (OSTI)

TMS Logo. About the 1996 International Symposium on Extraction and Processing for the Treatment and Minimization of Wastes: Treatment of Wastes...

42

Mercury Calibration System  

Science Conference Proceedings (OSTI)

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

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

2009-03-11T23:59:59.000Z

43

Process for low mercury coal  

DOE Patents (OSTI)

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

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

1995-04-04T23:59:59.000Z

44

Mercury Detection with Gold Nanoparticles  

E-Print Network (OSTI)

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

Crosby, Jeffrey

2013-01-01T23:59:59.000Z

45

Process for low mercury coal  

SciTech Connect

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

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

1995-01-01T23:59:59.000Z

46

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

Science Conference Proceedings (OSTI)

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

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

1995-07-01T23:59:59.000Z

47

Drinking Water Problems: Radionuclides  

E-Print Network (OSTI)

Radionuclides in drinking water can cause serious health problems for people. This publication explains what the sources of radionuclides in water are, where high levels have been found in Texas, how they affect health and how to treat water to remove them.

Lesikar, Bruce J.; Melton, Rebecca; Hare, Michael; Hopkins, Janie; Dozier, Monty

2006-08-04T23:59:59.000Z

48

Atmospheric Mercury Research Update  

Science Conference Proceedings (OSTI)

This report is a summary and analysis of research findings on utility and environmental mercury from 1997 to 2003. The update categorizes and describes recent work on mercury in utility-burned coal and its route through power plants, the measures for its control, and its fate in the environment following emissions from utility stacks. This fate includes atmospheric chemistry and transport, deposition to land and water surfaces, aquatic cycling, the dynamics of mercury in freshwater fish food webs, and th...

2004-03-30T23:59:59.000Z

49

Mercury Thermometer Alternatives Training  

Science Conference Proceedings (OSTI)

... tutorials are designed for educating various industrial user groups about the upcoming and current changes that ban the use of mercury products. ...

2013-06-04T23:59:59.000Z

50

MERCURY & DIMETHYLMERCURY EXPOSURE & EFFECTS  

SciTech Connect

This report identifies the dose response data available for several toxic mercury compounds and summarizes the symptoms and health effects associated with each of them.

HONEYMAN, J.O.

2005-12-13T23:59:59.000Z

51

Mercury Risk Assessment II  

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

Protection Agency in 2005, will require significant reductions in mercury emissions from coal-fired power plants. In formulating the regulations, a central point of debate...

52

Production of selenium-72 and arsenic-72  

DOE Patents (OSTI)

Methods and apparatus for producing selenium-72, separating it from its daughter isotope arsenic-72, and generating multiple portions of a solution containing arsenic-72 from a reusable parent substance comprised of selenium-72. The invention provides apparatus which can be located at a site where arsenic-72 is used, for purposes such as PET imaging, to produce arsenic-72 as needed, since the half-life of arsenic-72 is very short.

Phillips, Dennis R. (Los Alamos, NM)

1994-01-01T23:59:59.000Z

53

Production of selenium-72 and arsenic-72  

DOE Patents (OSTI)

Methods and apparatus for producing selenium-72, separating it from its daughter isotope arsenic-72, and generating multiple portions of a solution containing arsenic-72 from a reusable parent substance comprised of selenium-72. The invention provides apparatus which can be located at a site where arsenic-72 is used, for purposes such as PET imaging, to produce arsenic-72 as needed, since the half-life of arsenic-72 is very short.

Phillips, Dennis R. (Los Alamos, NM)

1995-01-01T23:59:59.000Z

54

Mercury Control Update 2009  

Science Conference Proceedings (OSTI)

EPRI has been evaluating cost-effective methods for reducing mercury emissions from coal-fired power plants. This report summarizes the current status of mercury control technologies and offers detailed discussion of boiler bromide addition balance-of-plant impacts and activated carbon injection (ACI) tests at selected sites.

2009-12-14T23:59:59.000Z

55

NETL: Mercury Emissions Control  

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

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

56

DOE Mercury Control Research  

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

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

57

Radionuclides Allyn H. Seymour  

Office of Legacy Management (LM)

Radionuclides Radionuclides Allyn H. Seymour in Air, Water, victor A. Nelson Laboratory of Radiation Ecology, University of and Biota Washington, Seattle, \\'ashington Air, water, and biological samples collected before and after the 1965, 1969, and 1971 underground nuclear detonations at Amchitka Island were analyzed for natural and fallout mdionrrclides b y gamma spectrometry. Selected samples were also analyzed for tritium, " ~ e , and 9 0 ~ r . The objectiues were t o search for and identify radio~tuclides of Amchitka origin in the samples and t o contribute t o the general knowledge of the distribatiotl of radionuclides in the enuironment. The collection of seafoods and the analyses of samples for radionuclides potentially available t o man through the food web were enrphasized, but other

58

ALTERNATIVE FIELD METHODS TO TREAT MERCURY IN SOIL  

Science Conference Proceedings (OSTI)

The Department of Energy (DOE) currently has mercury (Hg) contaminated materials and soils at the various sites. Figure 1-1 (from http://www.ct.ornl.gov/stcg.hg/) shows the estimated distribution of mercury contaminated waste at the various DOE sites. Oak Ridge and Idaho sites have the largest deposits of contaminated materials. The majorities of these contaminated materials are soils, sludges, debris, and waste waters. This project concerns treatment of mercury contaminated soils. The technology is applicable to many DOE sites, in-particular, the Y-12 National Security Complex in Oak Ridge Tennessee and Idaho National Engineering and Environmental Laboratory (INEEL). These sites have the majority of the soils and sediments contaminated with mercury. The soils may also be contaminated with other hazardous metals and radionuclides. At the Y12 plant, the baseline treatment method for mercury contaminated soil is low temperature thermal desorption (LTTD), followed by on-site landfill disposal. LTTD is relatively expensive (estimated cost of treatment which exclude disposal cost for the collect mercury is greater than $740/per cubic yard [cy] at Y-12), does not treat any of the metal or radionuclides. DOE is seeking a less costly alternative to the baseline technology. As described in the solicitation (DE-RA-01NT41030), this project initially focused on evaluating cost-effective in-situ alternatives to stabilize or remove the mercury (Hg) contamination from high-clay content soil. It was believed that ex-situ treatment of soil contaminated with significant quantities of free-liquid mercury might pose challenges during excavation and handling. Such challenges may include controlling potential mercury vapors and containing liquid mercury beads. As described below, the focus of this project was expanded to include consideration of ex-situ treatment after award of the contract to International Technology Corporation (IT). After award of the contract, IT became part of Shaw E&I. The company will be denoted as ''IT'' for the rest of the document since the original contract was awarded to IT. This report details IT, Knoxville, TN and its subcontractor Nuclear Fuels Services (NFS) study to investigate alternative mercury treatment technology. The IT/NFS team demonstrated two processes for the amalgamation/stabilization/fixation of mercury and potentially Resource Conservation Recovery Act (RCRA) and radionuclide-contaminated soils. This project was to identify and demonstrate remedial methods to clean up mercury-contaminated soil using established treatment chemistries on soil from the Oak Ridge Reservation, Y-12 National Security Complex, the off-site David Witherspoon properties, and/or other similarly contaminated sites. Soil from the basement of Y-12 Plant Alpha 2 Building at the Oak Ridge Reservation was received at IT and NFS on December 20, 2001. Soils from the other locations were not investigated. The soil had background levels of radioactivity and had all eight RCRA metals well below the Toxicity Characteristic (TC) criteria. This project addresses the new DOE Environmental Management Thrust 2 ''Alternative Approaches to Current High Risk/High Cost Baselines''. Successful completion of this project will provide a step-change in DOE's treatment ability.

Ernie F. Stine

2002-08-14T23:59:59.000Z

59

Definition: Mercury Vapor | Open Energy Information  

Open Energy Info (EERE)

Mercury Vapor Jump to: navigation, search Dictionary.png Mercury Vapor Mercury is discharged as a highly volatile vapor during hydrothermal activity and high concentrations in...

60

Mercury Sensing with Optically Responsive Gold Nanoparticles  

E-Print Network (OSTI)

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

James, Jay Zachary

2012-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Method and apparatus for separating radionuclides from non-radionuclides  

DOE Patents (OSTI)

In an apparatus for separating radionuclides from non-radionuclides in a mixture of nuclear waste, a vessel is provided wherein the mixture is heated to a temperature greater than the temperature of vaporization for the non-radionuclides but less than the temperature of vaporization for the radionuclides. Consequently the non-radionuclides are vaporized while the non-radionuclides remain the solid or liquid state. The non-radionuclide vapors are withdrawn from the vessel and condensed to produce a flow of condensate. When this flow decreases the heat is reduced to prevent temperature spikes which might otherwise vaporize the radionuclides. The vessel is removed and capped with the radioactive components of the apparatus and multiple batches of the radionuclide residue disposed therein. Thus the vessel ultimately provides a burial vehicle for all of the radioactive components of the process.

Harp, Richard J. (18746 Viking Way, Cerritos, CA 90701)

1990-01-01T23:59:59.000Z

62

Radionuclide Air Emission Report for 2007  

E-Print Network (OSTI)

for Emissions of Radionuclides Other Than Radon FromHazardous Air Pollutants (Radionuclides), Availability ofLBNL to Revise Its Radionuclide NESHAP Monitoring Approach,

Wahl, Linnea

2008-01-01T23:59:59.000Z

63

Radionuclide Air Emission Report for 2009  

E-Print Network (OSTI)

the public from airborne radionuclide emissions. We requestfor Emissions of Radionuclides Other Than Radon FromFugitive Air Emissions of Radionuclides from Diffuse Sources

Wahl, Linnea

2010-01-01T23:59:59.000Z

64

Radionuclide Air Emission Report for 2011  

E-Print Network (OSTI)

LBNL-470E-201 Radionuclide Air Emission Report for Preparedfor Emissions of Radionuclides Other Than Radon FromFugitive Air Emissions of Radionuclides from Diffuse Sources

Wahl, Linnea

2012-01-01T23:59:59.000Z

65

Radionuclide Air Emission Report for 2008  

E-Print Network (OSTI)

Fugitive Air Emissions of Radionuclides from Diffuse SourcesHazardous Air Pollutants (Radionuclides), Availability ofLBNL to Revise Its Radionuclide NESHAP Monitoring Approach,

Wahl, Linnea

2009-01-01T23:59:59.000Z

66

Production of selenium-72 and arsenic-72  

SciTech Connect

Methods for producing selenium-72, separating it from its daughter isotope arsenic-72, and generating multiple portions of a solution containing arsenic-72 from a reusable parent substance comprised of selenium-72.

Phillips, Dennis R. (Los Alamos, NM)

1993-01-01T23:59:59.000Z

67

Recovery of mercury from mercury compounds via electrolytic methods  

DOE Patents (OSTI)

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

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

1988-01-01T23:59:59.000Z

68

Recovery of mercury from mercury compounds via electrolytic methods  

DOE Patents (OSTI)

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

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

1989-11-07T23:59:59.000Z

69

Recovery of mercury from mercury compounds via electrolytic methods  

DOE Patents (OSTI)

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

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

1989-01-01T23:59:59.000Z

70

Recovery of mercury from mercury compounds via electrolytic methods  

DOE Patents (OSTI)

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

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

1991-01-01T23:59:59.000Z

71

Recovery of mercury from mercury compounds via electrolytic methods  

DOE Patents (OSTI)

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

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

1991-06-18T23:59:59.000Z

72

Arsenic in human history and modern societies  

Science Conference Proceedings (OSTI)

Chapter 5 contains a section titled: Arsenic in coal and oil shale utilization and their by-products.

Kevin R. Henke; David A. Atwood [University of Kentucky, Lexington, KY (United States). Dept. of Chemistry

2009-03-15T23:59:59.000Z

73

Mercury Risk Assessment  

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

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

74

Mercury Control Update 2010  

Science Conference Proceedings (OSTI)

A February 2008 decision by the U.S. District of Columbia Circuit Court of Appeals remanded the Clean Air Mercury Rule back to the U.S. Environmental Protection Agency, opening the possibility of more stringent federal emission limits similar to those already adopted by some states. To meet these stringent limits, high mercury removals based on Maximum Achievable Control Technology for individual power plants may be needed. To help electric power companies comply with tightening emission standards in a ...

2010-12-31T23:59:59.000Z

75

Prediction of the thermodynamic properties of gold, arsenic, and  

Office of Scientific and Technical Information (OSTI)

The Hydrothermal Chemistry of Gold, Arsenic, Antimony, Mercury and Silver Brad Bessinger Exponent, Inc. 5335 Meadows Road, Suite 365 Lake Oswego, OR 97035 John A. Apps Earth Sciences Division Lawrence Berkeley National Laboratory University of California, Berkeley, California 94720 March 2005 This work was supported by the Director, Office of Science Office of Basic Energy Sciences of the U.S. Department of Energy under Contract No. DE-AC03-76SF00098. Abstract A comprehensive thermodynamic database based on the Helgeson-Kirkham-Flowers (HKF) equation of state was developed for metal complexes in hydrothermal systems. Because this equation of state has been shown to accurately predict standard partial molal thermodynamic properties of

76

Radionuclide Ratio Analyst Tool  

E-Print Network (OSTI)

Kendra M. Foltz Biegalski This memo recommends the installation of several upgrades and additions to the Radionuclide Monitoring Software (RMS) into operations at the Center for Monitoring Research (CMR). The software additions and upgrades described herein provide new functionality and improved results to many aspects of radionuclide data analysis. This software was developed under the Technical Verification and Analytical Support (TVAS) program at the CMR. This software has been running on the TVAS development network from 3 months to 2 years. Statement of Objective The objective of this proposal is the implementation of additions and upgrades to the RMS software into CMR operations. The following additional software components are recommended:

unknown authors

2002-01-01T23:59:59.000Z

77

Method and apparatus for monitoring mercury emissions  

DOE Patents (OSTI)

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

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

1997-10-21T23:59:59.000Z

78

Method and apparatus for monitoring mercury emissions  

DOE Patents (OSTI)

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

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

1997-01-01T23:59:59.000Z

79

ALTERNATIVE FIELD METHODS TO TREAT MERCURY IN SOIL  

Science Conference Proceedings (OSTI)

U.S. Department of Energy (DOE) used large quantities of mercury in the uranium separating process from the 1950s until the late 1980s in support of national defense. Some of this mercury, as well as other hazardous metals and radionuclides, found its way into, and under, several buildings, soil and subsurface soils and into some of the surface waters. Several of these areas may pose potential health or environmental risks and must be dealt with under current environmental regulations. DOE's National Energy Technology Laboratory (NETL) awarded a contract ''Alternative Field Methods to Treat Mercury in Soil'' to IT Group, Knoxville TN (IT) and its subcontractor NFS, Erwin, TN to identify remedial methods to clean up mercury-contaminated high-clay content soils using proven treatment chemistries. The sites of interest were the Y-12 National Security Complex located in Oak Ridge, Tennessee, the David Witherspoon properties located in Knoxville, Tennessee, and at other similarly contaminated sites. The primary laboratory-scale contract objectives were (1) to safely retrieve and test samples of contaminated soil in an approved laboratory and (2) to determine an acceptable treatment method to ensure that the mercury does not leach from the soil above regulatory levels. The leaching requirements were to meet the TC (0.2 mg/l) and UTS (0.025 mg/l) TCLP criteria. In-situ treatments were preferred to control potential mercury vapors emissions and liquid mercury spills associated with ex-situ treatments. All laboratory work was conducted in IT's and NFS laboratories. Mercury contaminated nonradioactive soil from under the Alpha 2 building in the Y-12 complex was used. This soils contained insufficient levels of leachable mercury and resulted in TCLP mercury concentrations that were similar to the applicable LDR limits. The soil was spiked at multiple levels with metallic (up to 6000 mg/l) and soluble mercury compounds (up to 500 mg/kg) to simulate expected ranges of mercury contamination and to increase the TCLP mercury values. IT/NFS investigated ambient temperature amalgamation/stabilization/fixation of mercury-contaminated soils to meet these objectives. Treatment ranged in size from a few ounces to 10 pounds. The treatability study philosophy was to develop working envelops of formulations where reasonable minimum and maximum amounts of each reagent that would successfully treat the contaminated soil were determined. The dosages investigated were based on ratios of stoichiometric reactions and applications of standard sets of formulations. The approach purposely identified formulations that failed short or longer cure-time performance criteria to define the limits of the envelope. Reagent envelops successfully met the project requirements one day after treatment and after greater than 30-day cures. The use of multiple levels of spikes allowed the establishment of reagent dosages that were successful across a broad range of mercury values, e.g., 50 to 6000 mg/kg mercury. The treatment products were damp to slightly wet material. Enough drying reagent, e.g., Portland cement or lime by-product, were added to some formulations to control the leachability of uranium and other hazardous metals and to ensure the product passed the paint filter test. Cost analyzes and conceptual designs for four alternatives for full-scale treatments were prepared. The alternatives included two in-situ treatments and two ex-situ treatments. The cost estimates were based on the results from the bench-scale study. All four alternatives treatment costs were well below the baseline costs.

Ernest F. Stine Jr; Steven T. Downey

2002-08-14T23:59:59.000Z

80

NETL: Mercury Emissions Inactive Mercury Projects  

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

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

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Speciation and Attenuation of Arsenic and Selenium at Coal Combustion By-Product Management Facilities  

Science Conference Proceedings (OSTI)

The overall objective of this project was to evaluate the impact of key constituents captured from power plant air streams (principally arsenic and selenium) on the disposal and utilization of coal combustion products (CCPs). Specific objectives of the project were: (1) to develop a comprehensive database of field leachate concentrations at a wide range of CCP management sites, including speciation of arsenic and selenium, and low-detection limit analyses for mercury; (2) to perform detailed evaluations of the release and attenuation of arsenic species at three CCP sites; and (3) to perform detailed evaluations of the release and attenuation of selenium species at three CCP sites. Each of these objectives was accomplished using a combination of field sampling and laboratory analysis and experimentation. All of the methods used and results obtained are contained in this report. For ease of use, the report is subdivided into three parts. Volume 1 contains methods and results for the field leachate characterization. Volume 2 contains methods and results for arsenic adsorption. Volume 3 contains methods and results for selenium adsorption.

K. Ladwig

2005-12-31T23:59:59.000Z

82

The studying of washing of arsenic and sulfur from coals having different ranges of arsenic contents  

SciTech Connect

To study the effectiveness of washing in removal of arsenic and sulfur from coals with different ranges of arsenic concentration, coal was divided into three groups on the basis of arsenic content: 0-5.5 mg/kg, 5.5 mg/kg-8.00 mg/kg, and over 8.00 mg/kg. The result shows that the arsenic in coals with higher arsenic content occurs mainly in an inorganic state and can be relatively easily removed. Arsenic removal is very difficult and less complete when the arsenic content is lower than 5.5 mg/kg because most of this arsenic is in an organic state. There is no relationship between washing rate of total sulfur and arsenic content, but the relationship between the washing rate of total sulfur and percent of organic sulfur is very strong.

Mingshi Wang; Dangyu Song; Baoshan Zheng; R.B. Finkelman [Institute of Geochemistry, Guiyang (China). State Key Lab of Environmental Geochemistry

2008-10-15T23:59:59.000Z

83

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

Open Energy Info (EERE)

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

84

ORNL DAAC Announces Mercury EOS  

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

Announces Mercury EOS Search and Order April 21, 2003: Mercury EOS, the ORNL DAAC's new search and order system that works with NASA's EOS ClearingHouse (ECHO), is now operational....

85

Dynamic Mercury Cycling Model Upgrade  

Science Conference Proceedings (OSTI)

This technical update describes the status of activities to upgrade the Dynamic Mercury Cycling Model (D-MCM), an EPRI simulation model that predicts mercury cycling and bioaccumulation in lakes.

2008-12-17T23:59:59.000Z

86

Groundwater Discharge of Mercury to California Coastal Waters  

E-Print Network (OSTI)

too much is consumed. This toxic form of mercury is producedfrom inorganic mercury by sulfur- and iron-reducing bacteriadischarge of total mercury and monomethyl mercury to central

Flegal, Russell; Paytan, Adina; Black, Frank

2009-01-01T23:59:59.000Z

87

Gas Mileage of 1994 Vehicles by Mercury  

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

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

88

Gas Mileage of 1985 Vehicles by Mercury  

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

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

89

Water displacement mercury pump  

DOE Patents (OSTI)

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

Nielsen, Marshall G. (Woodside, CA)

1985-01-01T23:59:59.000Z

90

Water displacement mercury pump  

DOE Patents (OSTI)

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

Nielsen, M.G.

1984-04-20T23:59:59.000Z

91

NETL: Mercury Emissions Control Technologies - Oxidation of Mercury Across  

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

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

92

SAP for Mercury Control  

Science Conference Proceedings (OSTI)

EPRI and the Illinois State Geological Survey (ISGS) have developed and patented a technology for the on-site production of activated carbon (AC). The basic approach of the sorbent activation process (SAP) is to use coal from the plant site to form AC for direct injection into flue gas, upstream of the particulate control device, for mercury adsorption. The SAP is designed to help significantly reduce the cost of AC for power plant mercury control. This report summarizes laboratory and Phase 1 field test...

2009-06-17T23:59:59.000Z

93

Mercury Controls Update 2011  

Science Conference Proceedings (OSTI)

In light of the proposed Maximum Achievable Control Technology (MACT) ruling for hazardous air pollutants (HAPs) issued by the U.S. Environmental Protection Agency on March 16, 2011, the requirement to reduce emissions of mercury and other HAPs is one of the key challenges for coal-fired power plants. The proposed MACT ruling limits mercury emissions to 1.2 lb/TBtu at the stack (4.0 lb/TBtu for lignite-fired units), based on a 30-day rolling average including startup and shutdown periods. To help electri...

2011-12-21T23:59:59.000Z

94

Mercury in FGD Byproducts  

Science Conference Proceedings (OSTI)

This report provides interim results from two EPRI co-funded projects that pertain to what happens to mercury in flue gas from coal-fired power boilers when the scrubbed by wet flue gas desulfurization (FGD) systems. The first project is co-sponsored by the U.S. Department of Energy's National Energy Technology Laboratory (NETL) and by USG Corporation under Cooperative Agreement DE-FC26-04NT42080, "Fate of Mercury in Synthetic Gypsum Used for Wallboard Production." The second project is being co-sponsore...

2005-12-07T23:59:59.000Z

95

Mercury Vapor | Open Energy Information  

Open Energy Info (EERE)

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

96

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

97

Gas Mileage of 1986 Vehicles by Mercury  

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

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

98

Gas Mileage of 1991 Vehicles by Mercury  

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

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

99

Method and apparatus for sampling atmospheric mercury  

DOE Patents (OSTI)

A method of simultaneously sampling particulate mercury, organic mercurial vapors, and metallic mercury vapor in the working and occupational environment and determining the amount of mercury derived from each such source in the sampled air. A known volume of air is passed through a sampling tube containing a filter for particulate mercury collection, a first adsorber for the selective adsorption of organic mercurial vapors, and a second adsorber for the adsorption of metallic mercury vapor. Carbon black molecular sieves are particularly useful as the selective adsorber for organic mercurial vapors. The amount of mercury adsorbed or collected in each section of the sampling tube is readily quantitatively determined by flameless atomic absorption spectrophotometry.

Trujillo, Patricio E. (Santa Fe, NM); Campbell, Evan E. (Los Alamos, NM); Eutsler, Bernard C. (Los Alamos, NM)

1976-01-20T23:59:59.000Z

100

Arsenic Remediation of Bangladesh Drinking Water using Iron-oxide...  

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

Arsenic Remediation of Bangladesh Drinking Water using Iron-oxide Coated Coal Ash Title Arsenic Remediation of Bangladesh Drinking Water using Iron-oxide Coated Coal Ash...

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Design of a rural water provision system to decrease arsenic...  

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

Lawrence Berkeley National Laboratory have invented ARUBA (Arsenic Removal Using Bottom Ash) a material that effectively and affordably removes high concentrations of arsenic from...

102

Method of arsenic removal from water  

DOE Patents (OSTI)

A method for low-cost arsenic removal from drinking water using chemically prepared bottom ash pre-treated with ferrous sulfate and then sodium hydroxide. Deposits on the surface of particles of bottom ash form of activated iron adsorbent with a high affinity for arsenic. In laboratory tests, a miniscule 5 grams of pre-treated bottom ash was sufficient to remove the arsenic from 2 liters of 2400 ppb (parts per billion) arsenic-laden water to a level below 50 ppb (the present United States Environmental Protection Agency limit). By increasing the amount of pre-treated bottom ash, even lower levels of post-treatment arsenic are expected. It is further expected that this invention supplies a very low-cost solution to arsenic poisoning for large population segments.

Gadgil, Ashok (El Cerrito, CA)

2010-10-26T23:59:59.000Z

103

Mercury Information Clearinghouse  

SciTech Connect

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

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

2006-03-31T23:59:59.000Z

104

Modeling Arsenic Fate and Transport in Groundwater  

Science Conference Proceedings (OSTI)

The fate of arsenic in the environment depends on a variety of geochemical factors, including pH, oxidation and reduction potential, and the presence of competing solutes such as phosphates. Methods of predicting arsenic fate and transport are evolving to incorporate sophisticated geochemical simulations. While contaminant transport codes that utilize adsorption isotherm equations may be inadequate for arsenic prediction in certain cases, they may be very powerful tools in others. This report describes t...

2006-08-16T23:59:59.000Z

105

Arsenic Remediation Technologies for Groundwater and Soil  

Science Conference Proceedings (OSTI)

In October 2003, the Electric Power Research Institute (EPRI) released report 1008881, Arsenic Remediation Technologies for Soils and Groundwater. The report provides a review of available technologies for the remediation of arsenic in soils, groundwater, and surface water, primarily at substation sites. In most cases, the technologies reviewed are applicable to a much wider range of projects. In the six years since the publication of that report, the technologies for the remediation of arsenic have cont...

2009-09-22T23:59:59.000Z

106

Environmental Chemistry of Arsenic: A Literature Review  

Science Conference Proceedings (OSTI)

Arsenic is an element of significant interest to energy companies because of its occurrence in coal ash and its potential for release and migration in groundwater. This report summarizes technical information on the environmental chemistry of arsenic assembled from an extensive literature review. In particular, the report provides an in-depth look at the three most important sets of geochemical reactions relevant to understanding the environmental chemistry of arsenic -- precipitation-dissolution, reduct...

2000-12-15T23:59:59.000Z

107

Electrochemical Arsenic Remediation for Rural Bangladesh  

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

Electrochemical Arsenic Remediation for Rural Bangladesh NOTICE Due to the current lapse of federal funding, Berkeley Lab websites are accessible, but may not be updated until...

108

Cleaning Arsenic from Bangladesh's Water : Future Technologies...  

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

Galitsky testing ARUBA in the lab. Scientist testing Arsenic Removal Using Bottom Ash (ARUBA) at the Berkeley Lab. Graph illustrating how well the ARUBA filtering sytems...

109

Berkeley Arsenic Alleviation Group - Lawrence Berkeley National ...  

the next house and use their neighbors well, thus negating the need for an arsenic?free water source. However ...

110

EBS Radionuclide Transport Abstraction  

Science Conference Proceedings (OSTI)

The purpose of this report is to develop and analyze the engineered barrier system (EBS) radionuclide transport abstraction model, consistent with Level I and Level II model validation, as identified in ''Technical Work Plan for: Near-Field Environment and Transport: Engineered Barrier System: Radionuclide Transport Abstraction Model Report Integration'' (BSC 2005 [DIRS 173617]). The EBS radionuclide transport abstraction (or EBS RT Abstraction) is the conceptual model used in the total system performance assessment for the license application (TSPA-LA) to determine the rate of radionuclide releases from the EBS to the unsaturated zone (UZ). The EBS RT Abstraction conceptual model consists of two main components: a flow model and a transport model. Both models are developed mathematically from first principles in order to show explicitly what assumptions, simplifications, and approximations are incorporated into the models used in the TSPA-LA. The flow model defines the pathways for water flow in the EBS and specifies how the flow rate is computed in each pathway. Input to this model includes the seepage flux into a drift. The seepage flux is potentially split by the drip shield, with some (or all) of the flux being diverted by the drip shield and some passing through breaches in the drip shield that might result from corrosion or seismic damage. The flux through drip shield breaches is potentially split by the waste package, with some (or all) of the flux being diverted by the waste package and some passing through waste package breaches that might result from corrosion or seismic damage. Neither the drip shield nor the waste package survives an igneous intrusion, so the flux splitting submodel is not used in the igneous scenario class. The flow model is validated in an independent model validation technical review. The drip shield and waste package flux splitting algorithms are developed and validated using experimental data. The transport model considers advective transport and diffusive transport from a breached waste package. Advective transport occurs when radionuclides that are dissolved or sorbed onto colloids (or both) are carried from the waste package by the portion of the seepage flux that passes through waste package breaches. Diffusive transport occurs as a result of a gradient in radionuclide concentration and may take place while advective transport is also occurring, as well as when no advective transport is occurring. Diffusive transport is addressed in detail because it is the sole means of transport when there is no flow through a waste package, which may dominate during the regulatory compliance period in the nominal and seismic scenarios. The advective transport rate, when it occurs, is generally greater than the diffusive transport rate. Colloid-facilitated advective and diffusive transport is also modeled and is presented in detail in Appendix B of this report.

J.D. Schreiber

2005-08-25T23:59:59.000Z

111

Clean process to destroy arsenic-containing organic compounds with recovery of arsenic  

DOE Patents (OSTI)

A reduction method is provided for the treatment of arsenic-containing organic compounds with simultaneous recovery of pure arsenic. Arsenic-containing organic compounds include pesticides, herbicides, and chemical warfare agents such as Lewisite. The arsenic-containing compound is decomposed using a reducing agent. Arsine gas may be formed directly by using a hydrogen-rich reducing agent, or a metal arsenide may be formed using a pure metal reducing agent. In the latter case, the arsenide is reacted with an acid to form arsine gas. In either case, the arsine gas is then reduced to elemental arsenic. 1 fig.

Upadhye, R.S.; Wang, F.T.

1996-08-13T23:59:59.000Z

112

Gas Mileage of 2002 Vehicles by Mercury  

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

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

113

Gas Mileage of 2008 Vehicles by Mercury  

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

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

114

Gas Mileage of 1987 Vehicles by Mercury  

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

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

115

Gas Mileage of 1990 Vehicles by Mercury  

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

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

116

Gas Mileage of 1999 Vehicles by Mercury  

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

1999 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1999 Mercury Cougar 4 cyl, 2.0 L, Automatic 4-spd, Regular Gasoline Compare 1999 Mercury Cougar View MPG Estimates Shared By...

117

Gas Mileage of 1984 Vehicles by Mercury  

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

4 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1984 Mercury Capri 4 cyl, 2.3 L, Automatic 3-spd, Regular Gasoline Compare 1984 Mercury Capri 18 City 20 Combined 22 Highway 1984...

118

Gas Mileage of 1988 Vehicles by Mercury  

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

8 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1988 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Regular Gasoline Compare 1988 Mercury Cougar 18 City 21 Combined 25 Highway 1988...

119

Gas Mileage of 1992 Vehicles by Mercury  

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

2 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1992 Mercury Capri 4 cyl, 1.6 L, Automatic 4-spd, Regular Gasoline Compare 1992 Mercury Capri View MPG Estimates Shared By Vehicle...

120

Gas Mileage of 1996 Vehicles by Mercury  

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

6 Mercury Vehicles EPA MPG MODEL City Comb Hwy 1996 Mercury Cougar 6 cyl, 3.8 L, Automatic 4-spd, Regular Gasoline Compare 1996 Mercury Cougar 17 City 19 Combined 24 Highway 1996...

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Gas Mileage of 2007 Vehicles by Mercury  

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

7 Mercury Vehicles EPA MPG MODEL City Comb Hwy 2007 Mercury Grand Marquis 8 cyl, 4.6 L, Automatic 4-spd, Regular Gasoline Compare 2007 Mercury Grand Marquis View MPG Estimates...

122

Recovery of mercury from acid waste residues  

DOE Patents (OSTI)

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

Greenhalgh, W.O.

1987-02-27T23:59:59.000Z

123

Recovery of mercury from acid waste residues  

DOE Patents (OSTI)

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

Greenhalgh, Wilbur O. (Richland, WA)

1989-01-01T23:59:59.000Z

124

Gas Mileage of 1989 Vehicles by Mercury  

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

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

125

Gas Mileage of 1993 Vehicles by Mercury  

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

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

126

FINAL REPORT SELECTION OF RADIONUCLIDES FOR  

E-Print Network (OSTI)

FINAL REPORT SELECTION OF RADIONUCLIDES FOR INCLUSION IN DOSE RECONSTRUCTIONS AT IDAHO NATIONAL Author: David C. Kocher SENES Oak Ridge, Inc. July 2005 #12;Selection of Radionuclides July 2005..................................................................................2 3.0 Selection of Radionuclides by Screening

127

Targeted radionuclide therapy  

Science Conference Proceedings (OSTI)

Targeted radionuclide therapy (TRT) seeks molecular and functional targets within patient tumor sites. A number of agents have been constructed and labeled with beta, alpha, and Auger emitters. Radionuclide carriers spanning a broad range of sizes; e.g., antibodies, liposomes, and constructs such as nanoparticles have been used in these studies. Uptake, in percent-injected dose per gram of malignant tissue, is used to evaluate the specificity of the targeting vehicle. Lymphoma (B-cell) has been the primary clinical application. Extension to solid tumors will require raising the macroscopic absorbed dose by several-fold over values found in present technology. Methods that may effect such changes include multistep targeting, simultaneous chemotherapy, and external sequestration of the agent. Toxicity has primarily involved red marrow so that marrow replacement can also be used to enhance future TRT treatments. Correlation of toxicities and treatment efficiency has been limited by relatively poor absorbed dose estimates partly because of using standard (phantom) organ sizes. These associations will be improved in the future by obtaining patient-specific organ size and activity data with hybrid SPECT/CT and PET/CT scanners.

Williams, Lawrence E.; DeNardo, Gerald L.; Meredith, Ruby F. [Radiology Division, City of Hope National Medical Center, Duarte, California 91010 (United States); Internal Medicine, University of California Davis Medical Center, 1508 Alhambra Boulevard, Suite 3100, Sacramento, California 95816 (United States); Department of Radiation Oncology, Wallace Tumor Institute WTI No. 117, University of Alabama at Birmingham, Birmingham, Alabama 35294 (United States)

2008-07-15T23:59:59.000Z

128

Public Health Guidance Note Mercury  

E-Print Network (OSTI)

Mercury (Hg) occurs in nature as the mineral cinnibar (red mercuric sulfide) and has found widespread use in industry. The commercial

unknown authors

2002-01-01T23:59:59.000Z

129

Drinking Water Problems: Radionuclides (Spanish)  

E-Print Network (OSTI)

Radionuclides in drinking water can cause serious health problems for people. This publication explains what the sources of radionuclides in water are, where high levels have been found in Texas, how they affect health and how to treat water to remove them.

Lesikar, Bruce J.; Melton, Rebecca; Hare, Michael; Hopkins, Janie; Dozier, Monty

2006-12-21T23:59:59.000Z

130

Method for mercury refinement  

DOE Patents (OSTI)

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

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

1991-01-01T23:59:59.000Z

131

Apparatus for mercury refinement  

DOE Patents (OSTI)

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

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

1991-01-01T23:59:59.000Z

132

Apparatus for mercury refinement  

DOE Patents (OSTI)

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

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

1991-07-16T23:59:59.000Z

133

PUBLIC HEALTH STATEMENT MERCURY  

E-Print Network (OSTI)

This Public Health Statement is the summary chapter from the Toxicological Profile for Mercury. It is one in a series of Public Health Statements about hazardous substances and their health effects. A shorter version, the ToxFAQs, is also available. This information is important because this substance may harm you. The effects of exposure to any hazardous substance depend on the dose, the duration, how you are exposed, personal traits and habits, and whether other chemicals are

unknown authors

1999-01-01T23:59:59.000Z

134

Method for mercury refinement  

DOE Patents (OSTI)

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

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

1991-04-09T23:59:59.000Z

135

Method for scavenging mercury  

DOE Patents (OSTI)

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

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

2010-07-13T23:59:59.000Z

136

Method for scavenging mercury  

SciTech Connect

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

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

2011-08-30T23:59:59.000Z

137

Method for scavenging mercury  

SciTech Connect

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

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

2009-01-20T23:59:59.000Z

138

Mercury Emissions Data Analyses  

Science Conference Proceedings (OSTI)

This report contains the visual materials included in presentations given at Research Triangle Park, North Carolina on April 3, 2002. Participants included representatives from EPRI, DOE, RMB Consulting & Research, and EERC. The MACT Working Group gave a presentation on "Variability in Hg Emissions Based on SCEM Data." The visuals in the report are a set of graphs documenting results of mercury emissions over time, using semi-continuous emissions monitor (SCEM) data. The EPA Utility Working Group gave a ...

2002-05-02T23:59:59.000Z

139

Process for upgrading arsenic-containing oils  

DOE Patents (OSTI)

A method is provided for avoiding feed-transfer-line plugging by a deposit comprising arsenic in hydroprocessing an oil containing an arsenic contaminant. In the method, a mixture of hydrogen gas and the oil is formed in situ in a bed of porous particulate contact material.

Sullivan, Richard F. (San Rafael, CA)

1979-01-01T23:59:59.000Z

140

Gas Mileage of 2000 Vehicles by Mercury  

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

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

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Gas Mileage of 2004 Vehicles by Mercury  

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

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

142

Gas Mileage of 1997 Vehicles by Mercury  

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

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

143

Gas Mileage of 2001 Vehicles by Mercury  

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

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

144

Gas Mileage of 1998 Vehicles by Mercury  

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

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

145

Gas Mileage of 2005 Vehicles by Mercury  

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

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

146

Gas Mileage of 1995 Vehicles by Mercury  

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

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

147

NETL: Mercury Emissions Control Technologies - Pilot Testing of Mercury  

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

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

148

NETL: Mercury Emissions Control Technologies - Evaluation of Mercury  

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

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

149

The Clean Air Mercury Rule  

SciTech Connect

Coming into force on July 15, 2005, the US Clean Air Mercury Rule will use a market-based cap-and-trade approach under Section 111 of the Clean Air Act to reduce mercury emissions from the electric power sector. This article provides a comprehensive summary of the new rule. 14 refs., 2 tabs.

Michael Rossler [Edison Electric Institute, Washington, DC (US)

2005-07-01T23:59:59.000Z

150

Carbonized material adsorbents for the removal of mercury from aqueous solutions  

SciTech Connect

Although wood has essentially been excluded as a starting material for the production of granular activated carbon because of the poor strength and friability of the products, powdered wood based activated carbons are still being used in water treatment and other liquid phase applications. However, the capability of powdered wood-based charcoal which in itself porous has not been fully known. Few studies have been conducted in harnessing its potential for adsorption purposes especially in water treatment. This study was conducted to investigate the possibility of using wood based carbonized materials from Sugi (Cryptomeria japonica D. Don) as adsorption materials in aqueous solutions of heavy metals like mercury, zinc, lead, cadmium and arsenic. However, of all the heavy metals investigated, mercury is considered to be the most toxic so this paper describes only the adsorption ability of the carbonized materials in adsorbing this metal from aqueous solutions of different concentrations.

Ishihara, S.; Pulido, L.L. [Kyoto Univ. (Japan); Kajimoto, T. [Wakayama Industrial Technology Center (Japan)

1996-12-31T23:59:59.000Z

151

Methods for dispensing mercury into devices  

DOE Patents (OSTI)

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

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

1987-04-28T23:59:59.000Z

152

Methods for dispensing mercury into devices  

DOE Patents (OSTI)

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

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

1987-04-28T23:59:59.000Z

153

Bioremediation of Metals and Radionuclides: What It Is and How It Works (2nd Edition)  

E-Print Network (OSTI)

63 ACRONYMS Radionuclides . . . . . . .5 The Focus on Radionuclides andand Radionuclides . . . . . . . . . . . . . . 56 Feature:

Palmisano, Anna; Hazen, Terry

2003-01-01T23:59:59.000Z

154

Fluorescent sensor for mercury  

DOE Patents (OSTI)

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

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

2011-11-22T23:59:59.000Z

155

Mercury Vapor (Kooten, 1987) | Open Energy Information  

Open Energy Info (EERE)

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

156

Recovery from Mercury Contamination in the Second Songhua River, China  

E-Print Network (OSTI)

K. , & Rubin, J. R. (2005). Mercury levels and relationshipsJ. , et al. (1999). Mercury in contaminated coastalEnvironmental costs of mercury pollution. Science of the

Zhang, Z. S.; Sun, X. J.; Wang, Q. C.; Zheng, D. M.; Zheng, N.; Lv, X. G.

2010-01-01T23:59:59.000Z

157

Mercury Isotope Fractionation by Environmental Transport and Transformation Processes  

E-Print Network (OSTI)

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

Koster van Groos, Paul Gijsbert

2011-01-01T23:59:59.000Z

158

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

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

of mercury. The primary pathway for mercury exposure is through consumption of fish. The most susceptible population to mercury exposure is the fetus. Therefore, the risk...

159

Radionuclide Retention in Concrete Wasteforms  

Science Conference Proceedings (OSTI)

Assessing long-term performance of Category 3 waste cement grouts for radionuclide encasement requires knowledge of the radionuclide-cement interactions and mechanisms of retention (i.e., sorption or precipitation); the mechanism of contaminant release; the significance of contaminant release pathways; how wasteform performance is affected by the full range of environmental conditions within the disposal facility; the process of wasteform aging under conditions that are representative of processes occurring in response to changing environmental conditions within the disposal facility; the effect of wasteform aging on chemical, physical, and radiological properties; and the associated impact on contaminant release. This knowledge will enable accurate prediction of radionuclide fate when the wasteforms come in contact with groundwater. The information present in the report provides data that (1) measures the effect of concrete wasteform properties likely to influence radionuclide migration; and (2) quantifies the rate of carbonation of concrete materials in a simulated vadose zone repository.

Bovaird, Chase C.; Jansik, Danielle P.; Wellman, Dawn M.; Wood, Marcus I.

2011-09-30T23:59:59.000Z

160

Electrochemical arsenic remediation for rural Bangladesh  

Science Conference Proceedings (OSTI)

Arsenic in drinking water is a major public health problem threatening the lives of over 140 million people worldwide. In Bangladesh alone, up to 57 million people drink arsenic-laden water from shallow wells. ElectroChemical Arsenic Remediation(ECAR) overcomes many of the obstacles that plague current technologies and can be used affordably and on a small-scale, allowing for rapid dissemination into Bangladesh to address this arsenic crisis. In this work, ECAR was shown to effectively reduce 550 - 580 mu g=L arsenic (including both As[III]and As[V]in a 1:1 ratio) to below the WHO recommended maximum limit of 10 mu g=L in synthetic Bangladesh groundwater containing relevant concentrations of competitive ions such as phosphate, silicate, and bicarbonate. Arsenic removal capacity was found to be approximately constant within certain ranges of current density, but was found to change substantially between ranges. In order of decreasing arsenic removal capacity, the pattern was: 0.02 mA=cm2> 0.07 mA=cm2> 0.30 - 1.1 mA=cm2> 5.0 - 100 mA=cm2. Current processing time was found to effect arsenic removal capacity independent of either charge density or current density. Electrode polarization studies showed no passivation of the electrode in the tested range (up to current density 10 mA=cm2) and ruled out oxygen evolution as the cause of decreasing removal capacity with current density. Simple settling and decantation required approximately 3 days to achieve arsenic removal comparable to filtration with a 0.1 mu m membrane. X-ray Absorption Spectroscopy (XAS) showed that (1) there is no significant difference in the arsenic removal mechanism of ECAR during operation at different current densities and (2) the arsenic removal mechanism in ECAR is consistent with arsenate adsorption onto a homogenous Fe(III)oxyhydroxide similar in structure to 2-line ferrihydrite. ECAR effectively reduced high arsenic concentrations (100 - 500 mu g=L) in real Bangladesh tube well water collected from three regions to below the WHO limit of 10 mu g=L. Prototype fabrication and field testing are currently underway.

Addy, Susan Amrose

2009-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Arsenic removal and stabilization by synthesized pyrite  

E-Print Network (OSTI)

Arsenic is ubiquitous whether it is naturally occurring or produced by humans. It is found at sites on the National Priority List and at sites operated by DOE, where it is the second most commonly found contaminant. More wastes containing arsenic will be produced due to the lowering of the Maximum Contaminant Level (MCL) for arsenic in drinking water which will result in more treatment facilities for arsenic removal that will generate residuals. Furthermore, arsenic can be released from such wastes under the reduced conditions that are found in landfills. Pyrite (FeS2) is believed to be a compound that has a high affinity for arsenic and is stable under anoxic conditions. The first task of this research was to develop a method for making pyrite crystals of defined size with minimal reaction time and at high yield. Effects on the synthesis of pyrite particles of pH, the ratio of Fe/S, temperature and reaction time were investigated in batch reactor systems. Pyrite was synthesized within 24 hours at pH values ranging from pH 3.6 through pH 5.6, and at a ratio of Fe/S of 0.5. X-ray diffraction and scanning electron microscopy were used to size and characterize the pyrite particles. Experimental and analytical procedures developed for this work, included a hydride generation atomic absorption spectrometry method for measuring arsenic species (As(III), As(V)). The synthesized pyrite was applied to remove arsenic and its maximum capacity for arsenic removal was measured in batch adsorption experiments to be 3.23 ?mol/g for As(III) and 113 ?mol/g for As(V). Information obtained on the characteristics of chemical species before and after the reaction with arsenic showed that iron and sulfur were oxidized. Last, how strongly arsenic was bound to pyrite was investigated and it was determined that release of arsenic from As(III)-pyrite is not affected by pH, but release from As(V)-pyrite is affected by pH with minimum release in the range pH 5 to pH 8.

Song, Jin Kun

2008-12-01T23:59:59.000Z

162

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

SciTech Connect

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

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

2007-07-01T23:59:59.000Z

163

MERCURY REMOVAL FROM DOE SOLID MIXED WASTE USING THE GEMEP(sm) TECHNOLOGY  

SciTech Connect

Under the sponsorship of the Federal Energy Technology Center (FETC), Metcalf and Eddy (M and E), in association with General Electric Corporate Research and Development Center (GE-CRD), Colorado Minerals Research Institute (CMRI), and Oak Ridge National Laboratory (ORNL), conducted laboratory-scale and bench-scale tests of the General Electric Mercury Extraction Process technology on two mercury-contaminated mixed solid wastes from U. S. Department of Energy sites: sediment from the East Fork of Poplar Creek, Oak Ridge (samples supplied by Oak Ridge National Laboratory), and drummed soils from Idaho National Environmental and Engineering Laboratory (INEEL). Fluorescent lamps provided by GE-CRD were also studied. The GEMEP technology, invented and patented by the General Electric Company, uses an extraction solution composed of aqueous potassium iodide plus iodine to remove mercury from soils and other wastes. The extraction solution is regenerated by chemical oxidation and reused, after the solubilized mercury is removed from solution by reducing it to the metallic state. The results of the laboratory- and bench-scale testing conducted for this project included: (1) GEMEP extraction tests to optimize extraction conditions and determine the extent of co-extraction of radionuclides; (2) pre-screening (pre-segregation) tests to determine if initial separation steps could be used effectively to reduce the volume of material needing GEMEP extraction; and (3) demonstration of the complete extraction, mercury recovery, and iodine recovery and regeneration process (known as locked-cycle testing).

1999-03-01T23:59:59.000Z

164

NETL: Mercury Emissions Control Technologies - Testing of Mercury Control  

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

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

165

MIGRATION OF RADIONUCLIDES THROUGH SORBING MEDIA ANALYTICAL SOLUTION - I  

E-Print Network (OSTI)

centration Phenomenon of Radionuclide Chain Migra- tion", B5only MIGRA'riON OF RADIONUCLIDES THROUGH SORBING MEDIATransport Equation for Radionuclide in Porous Media General

Harada, M.

2013-01-01T23:59:59.000Z

166

MIGRATION OF RADIONUCLIDES THROUGH SORBING MEDIA ANALYTICAL SOLUTIONS--II  

E-Print Network (OSTI)

for the Transport of Radionuclides and Their Decay ProductsVolume II MIGRATION OF RADIONUCLIDES THROUGH iORBING MEDIAAl. M. Albert, "Radionuclide Migration with Multidimensional

Pigford, T.H.

2010-01-01T23:59:59.000Z

167

Discovery of the Mercury Isotopes  

E-Print Network (OSTI)

Forty mercury isotopes have so far been observed; the discovery of these isotopes is discussed. For each isotope a brief summary of the first refereed publication, including the production and identification method, is presented.

D. Meierfrankenfeld; M. Thoennessen

2009-12-01T23:59:59.000Z

168

Mercury Control Technology Selection Guide  

Science Conference Proceedings (OSTI)

EPRI, the DOE National Energy Technology Laboratory, and various other organizations have undertaken extensive RD programs over the past decade to develop cost-effective methods for reducing mercury emissions from coal-burning power plants. The field tests sponsored by these organizations have produced a significant amount of pilot and full-scale mercury control data for a variety of technologies at power plant sites with different boiler types, firing different coals, and equipped with various air emiss...

2006-09-22T23:59:59.000Z

169

Mercury Stability in FGD Byproducts  

Science Conference Proceedings (OSTI)

A significant fraction of the mercury in coals fired for power generation currently is removed by wet flue gas desulfurization (FGD) systems and incorporated in the byproducts from those systems. This report summarizes the results of an EPRI-sponsored project to measure the stability of mercury in FGD byproducts from coal-fired generating plants under simulated landfill and reuse conditions. The current effort repeated portions of a 2003 project, documented in EPRI report 1004254, to determine whether th...

2004-03-24T23:59:59.000Z

170

Mercury Atomic Clock Sets Time-Keeping Record  

Science Conference Proceedings (OSTI)

Mercury Atomic Clock Sets Time-Keeping Record. ... A prototype mercury optical clock originally was demonstrated at NIST in 2000. ...

2013-08-27T23:59:59.000Z

171

Radionuclide Retention in Concrete Wasteforms  

SciTech Connect

Assessing long-term performance of Category 3 waste cement grouts for radionuclide encasement requires knowledge of the radionuclide-cement interactions and mechanisms of retention (i.e., sorption or precipitation); the mechanism of contaminant release; the significance of contaminant release pathways; how wasteform performance is affected by the full range of environmental conditions within the disposal facility; the process of wasteform aging under conditions that are representative of processes occurring in response to changing environmental conditions within the disposal facility; the effect of wasteform aging on chemical, physical, and radiological properties; and the associated impact on contaminant release. This knowledge will enable accurate prediction of radionuclide fate when the wasteforms come in contact with groundwater. Data collected throughout the course of this work will be used to quantify the efficacy of concrete wasteforms, similar to those used in the disposal of LLW and MLLW, for the immobilization of key radionuclides (i.e., uranium, technetium, and iodine). Data collected will also be used to quantify the physical and chemical properties of the concrete affecting radionuclide retention.

Wellman, Dawn M.; Jansik, Danielle P.; Golovich, Elizabeth C.; Cordova, Elsa A.

2012-09-24T23:59:59.000Z

172

Radionuclide detection devices and associated methods  

Science Conference Proceedings (OSTI)

Radionuclide detection devices comprise a fluid cell comprising a flow channel for a fluid stream. A radionuclide collector is positioned within the flow channel and configured to concentrate one or more radionuclides from the fluid stream onto at least a portion of the radionuclide collector. A scintillator for generating scintillation pulses responsive to an occurrence of a decay event is positioned proximate at least a portion of the radionuclide collector and adjacent to a detection system for detecting the scintillation pulses. Methods of selectively detecting a radionuclide are also provided.

Mann, Nicholas R. (Rigby, ID); Lister, Tedd E. (Idaho Falls, ID); Tranter, Troy J. (Idaho Falls, ID)

2011-03-08T23:59:59.000Z

173

Arsenic Geochemistry in Source Waters of the Los Angeles Aqueduct  

E-Print Network (OSTI)

has focused on arsenic geochemistry in natural waters. ThisG402 XU2-7 ARSENIC GEOCHEMISTRY IN SOURCE WATERS OF T H EOrganism Interactions, Geochemistry, Ground Water Quality,

Hering, Janet G; Wilkie, Jennifer A; Chiu, Van Q

1997-01-01T23:59:59.000Z

174

Solid materials for removing arsenic and method thereof  

Science Conference Proceedings (OSTI)

Solid materials have been developed to remove arsenic compounds from aqueous media. The arsenic is removed by passing the aqueous phase through the solid materials which can be in molded, granular, or powder form. The solid materials adsorb the arsenic leaving a purified aqueous stream. The materials are aerogels or xerogels and aerogels or xerogels and solid support structure, e.g., granulated activated carbon (GAC), mixtures. The species-specific adsorption occurs through specific chemical modifications of the solids tailored towards arsenic.

Coronado, Paul R. (Livermore, CA); Coleman, Sabre J. (Oakland, CA); Sanner, Robert D. (Livermore, CA); Dias, Victoria L. (Livermore, CA); Reynolds, John G. (San Ramon, CA)

2010-09-28T23:59:59.000Z

175

Solid materials for removing arsenic and method thereof  

DOE Patents (OSTI)

Solid materials have been developed to remove arsenic compounds from aqueous media. The arsenic is removed by passing the aqueous phase through the solid materials which can be in molded, granular, or powder form. The solid materials adsorb the arsenic leaving a purified aqueous stream. The materials are aerogels or xerogels and aerogels or xerogels and solid support structure, e.g., granulated activated carbon (GAC), mixtures. The species-specific adsorption occurs through specific chemical modifications of the solids tailored towards arsenic.

Coronado, Paul R. (Livermore, CA); Coleman, Sabre J. (Oakland, CA); Sanner, Robert D. (Livermore, CA); Dias, Victoria L. (Livermore, CA); Reynolds, John G. (San Ramon, CA)

2008-07-01T23:59:59.000Z

176

Disposable Absorbent Material for the Removal of Arsenic from Water  

Science Conference Proceedings (OSTI)

Soils and groundwater at many substation sites are contaminated with arsenic-containing compounds. Cost effective water treatment technologies are needed to remove arsenic and other trace metals from underlying aquifers, especially now that drinking water standard for arsenic has been lowered to 10 g/L from the previous value of 50 g/L. The current project tested a disposable ferric oxide adsorbent material, Bayoxide E33, which has been reported to have a high capacity for arsenic removal.

2008-09-10T23:59:59.000Z

177

Correlations Between Gene Expression and Mercury Levels in Blood of Boys With and Without Autism  

E-Print Network (OSTI)

AJ (2005) Inorganic mercury dissociates preassembledmetabolize toxicants, such as mercury, differently. RNA wasexpression microarrays. Mercury levels were measured using

2011-01-01T23:59:59.000Z

178

NETL: Mercury Emissions Control Technologies - Mercury Control For Plants  

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

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

179

Chemical Constituents in Coal Combustion Product Leachate: Arsenic  

Science Conference Proceedings (OSTI)

This report provides comprehensive information on the environmental behavior of arsenic. Included are discussions of arsenics occurrence in soil and water, occurrence in coal combustion products (CCPs), CCP leaching characteristics, effects on human health and ecology, geochemistry, and treatment/remediation options.

2008-11-25T23:59:59.000Z

180

Iron Biomineralization: Implications on the Fate of Arsenic in Landfills  

E-Print Network (OSTI)

these arsenic-bearing solid residuals (ABSR) pass the Toxicity Characteristic Leaching Procedure (TCLP in our laboratory as well as other labs, has shown that the TCLP greatly underestimates the ABSR leaching concentrations of As. Iron reduction led to arsenic release into solution, where arsenic was reduced. #12;Figure

Cushing, Jim. M.

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Radionuclide labeled lymphocytes for therapeutic use  

DOE Patents (OSTI)

Lymphocytes labelled with ..beta..-emitting radionuclides are therapeutically useful, particularly for lymphoid ablation. They are prepared by incubation of the lymphocytes with the selected radionuclide-oxine complex.

Srivastava, S.C.; Fawwaz, R.A.; Richards, P.

1983-05-03T23:59:59.000Z

182

Radionuclide labeled lymphocytes for therapeutic use  

DOE Patents (OSTI)

Lymphocytes labelled with .beta.-emitting radionuclides are therapeutically useful, particularly for lymphoid ablation. They are prepared by incubation of the lymphocytes with the selected radionuclide-oxine complex.

Srivastava, Suresh C. (Setauket, NY); Fawwaz, Rashid A. (Pelham, NY); Richards, Powell (Bayport, NY)

1985-01-01T23:59:59.000Z

183

Mercury switch with non-wettable electrodes  

DOE Patents (OSTI)

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

Karnowsky, M.M.; Yost, F.G.

1986-04-09T23:59:59.000Z

184

Mercury switch with non-wettable electrodes  

DOE Patents (OSTI)

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

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

1987-01-01T23:59:59.000Z

185

NETL: Emissions Characterization - Mercury Reactions in Power...  

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

Mercury Reactions in Power Plant Plumes: Bowen Study DOE-NETL is participating in a field study, managed by EPRI, to document the changes in mercury speciation that may be...

186

Mercury Solar Systems | Open Energy Information  

Open Energy Info (EERE)

OpenEI by expanding it. Mercury Solar Systems is a company located in New Rochelle, New York . References "Mercury Solar Systems" Retrieved from "http:en.openei.orgw...

187

Gas Mileage of 2009 Vehicles by Mercury  

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

Comb Hwy 2009 Mercury Grand Marquis FFV 8 cyl, 4.6 L, Automatic 4-spd, Regular Gas or E85 Compare 2009 Mercury Grand Marquis FFV Gas 16 City 19 Combined 24 Highway E85 12 City...

188

Gas Mileage of 2010 Vehicles by Mercury  

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

Comb Hwy 2010 Mercury Grand Marquis FFV 8 cyl, 4.6 L, Automatic 4-spd, Regular Gas or E85 Compare 2010 Mercury Grand Marquis FFV View MPG Estimates Shared By Vehicle Owners Gas...

189

Gas Mileage of 2011 Vehicles by Mercury  

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

Comb Hwy 2011 Mercury Grand Marquis FFV 8 cyl, 4.6 L, Automatic 4-spd, Regular Gas or E85 Compare 2011 Mercury Grand Marquis FFV View MPG Estimates Shared By Vehicle Owners Gas...

190

Gas Mileage of 2003 Vehicles by Mercury  

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

Highway 2003 Mercury Mountaineer 2WD FFV 6 cyl, 4.0 L, Automatic 5-spd, Regular Gas or E85 Compare 2003 Mercury Mountaineer 2WD FFV Gas 14 City 16 Combined 19 Highway E85 10 City...

191

Gas Mileage of 2006 Vehicles by Mercury  

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

23 Highway 2006 Mercury Grand Marquis 8 cyl, 4.6 L, Automatic 4-spd, Regular Gas or E85 Compare 2006 Mercury Grand Marquis Gas 15 City 18 Combined 23 Highway E85 11 City 13...

192

NIST Radionuclide Half-Life Measurements (HTML)  

Science Conference Proceedings (OSTI)

... Radionuclide, Number of Sources, Number of Half Lives Followed, Half Life *, Statistical Standard Uncertainty, Other Standard Uncertainty, References ...

2010-10-05T23:59:59.000Z

193

Radionuclide Sensors for Subsurface Water Monitoring  

SciTech Connect

Contamination of the subsurface by radionuclides is a persistent and vexing problem for the Department of Energy. These radionuclides must be measured in field studies and monitoed in the long term when they cannot be removed. However, no radionuclide sensors existed for groundwater monitoring prior to this team's research under the EMSP program Detection of a and b decays from radionuclides in water is difficult due to their short ranges in condensed media.

Timothy DeVol

2006-06-30T23:59:59.000Z

194

Method for the removal and recovery of mercury  

DOE Patents (OSTI)

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

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

1997-01-28T23:59:59.000Z

195

Method for the removal and recovery of mercury  

DOE Patents (OSTI)

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

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

1997-01-01T23:59:59.000Z

196

Mercury Oxidation Performance of Advanced SCR Catalyst  

Science Conference Proceedings (OSTI)

The ability of selective catalytic reduction (SCR) catalysts to oxidize mercury is an important aspect of many utilities mercury control strategies. Improved SCR mercury oxidation will facilitate its capture in downstream wetflue gas desulfurization systems and will generally result in lower emission rates. Recently, catalyst manufacturers have attempted to maximize mercury oxidation through advanced catalyst formulations.This study documents the performance of an advanced ...

2012-12-31T23:59:59.000Z

197

Transitioning from Mercury Thermometers to Alternative ...  

Science Conference Proceedings (OSTI)

... methods in the petroleum industry continue to specify mercury- in-glass thermometers. ... Thermometers are available from many commercial sources ...

2013-06-03T23:59:59.000Z

198

GUIDANCE ON IMPLEMENTING RADIONUCLIDE NESHAPS  

E-Print Network (OSTI)

- Radionuclide Emissions Other than Radon from DOE Facilities . . . . . . . . . . . . . . . . 13 2.2.2 Subpart I - NRC Licensed and Non-DOE Federal Facilities . . . . . . . . . . . . . . . . . . 14 2.3 NESHAPS Subpart I . . . . 44 3.2 Other NRC Licensees - 40 CFR 61 Subpart I . . . . . . 44 3.3 DOE Facilities

199

Mercury Continuous Emmission Monitor Calibration  

SciTech Connect

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

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

2009-03-12T23:59:59.000Z

200

Mercury Flux Measurements: An Intercomparison and Assessment: Nevada Mercury Emissions Project (NvMEP)  

Science Conference Proceedings (OSTI)

An understanding of the contribution of natural nonpoint mercury sources to regional and global atmospheric mercury pools is critical for developing emission inventories, formulating environmental regulations, and assessing human and ecological health risks. This report discusses the results of the Nevada Mercury Emissions Project (NvMEP) and takes a close look at the emerging technologies used to obtain mercury flux field data. In specific, it provides an intercomparison of mercury flux measurements obt...

1998-12-14T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Arsenic Speciation in Blue Mussels (Mytilus edulis) Along a Highly Contaminated Arsenic Gradient  

Science Conference Proceedings (OSTI)

Arsenic is naturally present in marine ecosystems, and these can become contaminated from mining activities, which may be of toxicological concern to organisms that bioaccumulate the metalloid into their tissues. The toxic properties of arsenic are dependent on the chemical form in which it is found (e.g., toxic inorganic arsenicals vs nontoxic arsenobetaine), and two analytical techniques, high performance liquid chromatography coupled with inductively coupled plasma mass spectrometry (HPLC-ICP-MS) and X-ray absorption spectroscopy (XAS), were used in the present study to examine the arsenic species distribution in blue mussels (Mytilus edulis) obtained from an area where there is a strong arsenic concentration gradient as a consequence of mining impacted sediments. A strong positive correlation was observed between the concentration of inorganic arsenic species (arsenic compounds with no As-C bonds) and total arsenic concentrations present in M. edulis tissues (R{sup 2} = 0.983), which could result in significant toxicological consequences to the mussels and higher trophic consumers. However, concentrations of organoarsenicals, dominated by arsenobetaine, remained relatively constant regardless of the increasing As concentration in M. edulis tissue (R{sup 2} = 0.307). XANES bulk analysis and XAS two-dimensional mapping of wet M. edulis tissue revealed the presence of predominantly arsenic-sulfur compounds. The XAS mapping revealed that the As(III)-S and/or As(III) compounds were concentrated in the digestive gland. However, arsenobetaine was found in small and similar concentrations in the digestive gland as well as the surrounding tissue suggesting arsenobetaine may being used in all of the mussel's cells in a physiological function such as an intracellular osmolyte.

Whaley-Martin, K.J.; Koch, I.; Moriarty, M.; Reimer, K.J. (Royal)

2012-11-01T23:59:59.000Z

202

Lumex Mercury CEM  

E-Print Network (OSTI)

Program to facilitate the deployment of innovative or improved environmental technologies through performance verification and dissemination of information. The goal of the ETV Program is to further environmental protection by substantially accelerating the acceptance and use of improved and cost-effective technologies. ETV seeks to achieve this goal by providing high-quality, peer-reviewed data on technology performance to those involved in the design, distribution, financing, permitting, purchase, and use of environmental technologies. ETV works in partnership with recognized standards and testing organizations; with stakeholder groups that consist of buyers, vendor organizations, and permitters; and with the full participation of individual technology developers. The program evaluates the performance of innovative technologies by developing test plans that are responsive to the needs of stakeholders, conducting field or laboratory tests (as appropriate), collecting and analyzing data, and preparing peer-reviewed reports. All evaluations are conducted in accordance with rigorous quality assurance protocols to ensure that data of known and adequate quality are generated and that the results are defensible. The Advanced Monitoring Systems (AMS) Center, one of six technology centers under ETV, is operated by Battelle in cooperation with EPAs National Exposure Research Laboratory. The AMS Center has recently evaluated the performance of continuous emission monitors used to measure mercury in flue gases. This

unknown authors

2001-01-01T23:59:59.000Z

203

DFJ Mercury | Open Energy Information  

Open Energy Info (EERE)

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

204

Apparatus for control of mercury  

DOE Patents (OSTI)

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

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

2001-01-01T23:59:59.000Z

205

Mercury and platinum abundances in mercury-manganese stars  

E-Print Network (OSTI)

We report new results for the elemental and isotopic abundances of the normally rare elements mercury and platinum in HgMn stars. Typical overabundances can be 4 dex or more. The isotopic patterns do not follow the fractionation model of White et al (1976).

C. M. Jomaron; M. M. Dworetsky; D. A. Bohlender

1998-05-06T23:59:59.000Z

206

NETL: Mercury Emissions Control Technologies - Advanced Mercury Sorbents  

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

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

207

Fate of soluble uranium in the I{sub 2}/KI leaching process for mercury removal  

SciTech Connect

General Electric Corporation has developed an extraction and recovery system for mercury, based upon the use of iodine (oxidant) and iodide ion (complexing agent). This system has been proposed for application to select mercury-contaminated mixed waste (i.e., waste containing radionuclides as well as other hazardous constituents), which have been generated by historic activities in support of US Department of Energy (DOE) missions. This system is compared to a system utilizing hypochlorite and chloride ions for removal of mercury and uranium from a sample of authentic mixed waste sludge. Relative to the hypochlorite (bleach) system, the iodine system mobilized more mercury and less uranium from the sludge. An engineering flowsheet has been developed to treat spent iodine-containing extraction medium, allowing the system to be recycled. The fate of soluble uranium in this series of treatment unit operations was monitored by tracing isotopically-enriched uranyl ion into simulated spent extraction medium. Treatment with use of elemental iron is shown to remove > 85% of the traced uranium while concurrently reducing excess iodine to the iodide ion. The next unit operation, adjustment of the solution pH to a value near 12 by the addition of lime slurry to form a metal-laden sludge phase (an operation referred to as lime-softening), removed an additional 57% of soluble uranium activity, for an over-all removal efficiency of {approximately} 96%. However, the precipitated solids did not settle well, and some iodide reagent is held up in the wet filtercake.

Bostick, W.D.; Davis, W.H.; Jarabek, R.J. [East Tennessee Technology Park, Oak Ridge, TN (United States). Materials and Chemistry Lab.

1997-09-01T23:59:59.000Z

208

Natural chelates for radionuclide decorporation  

DOE Patents (OSTI)

This invention relates to the method and resulting chelates of desorbing a radionuclide selected from thorium, uranium, and plutonium containing cultures in a bioavailable form involving pseudomonas or other microorganisms. A preferred microorganism is Pseudomonas aeruginosa which forms multiple chelates with thorium in the range of molecular weight 1000 to 1000 and also forms chelates with uranium of molecular weight in the area of 100 to 1000 and 1000 to 2000.

Premuzic, E.T.

1983-08-25T23:59:59.000Z

209

Radionuclide behavior in the environment  

Science Conference Proceedings (OSTI)

The purpose of this report is to document the results of the following task: Review for quality and consistency the available data on measurements of initial ground contamination of Chernobyl radionuclides in various parts of Norway and subsequent concentrations of these radionuclides in various environmental media as functions of time. Utilize the data obtained to verify the existing models, or to improve them, for describing radionuclide behavior in the environment. Some of the processes standard were: migration into soil; weathering; resuspension; food-chain contamination; and loss or reconcentration by run-off. The task performed within this contract has been to use post-Chernobyl data from Norway to verify or find areas for possible improvement in the chronic exposure pathway models utilized in MACCS. Work has consisted mainly of collecting and evaluating post-Chernobyl information from Norway or other countries when relevant; but has also included experimental work performed specifically for the current task. In most connections the data available show the models and data in MACCS to be appropriate. A few areas where the data indicate that the MACCS approach is faulty or inadequate are, however, pointed out in the report. These should be examined carefully, and appropriate modifications should eventually be made. 14 refs., 12 figs., 22 tabs.

Tveten, U. (Institutt for Energiteknikk, Kjeller (Norway))

1991-09-01T23:59:59.000Z

210

Bioremediation of metals and radionuclides: What it is and How it Works  

E-Print Network (OSTI)

Restoration Objectives. The Focus on Radionuclides andAFFECTING METALS AND RADIONUCLIDES THE BIOREMEDIATION OFOF METALS RADIONUCLIDES Scope of Problem . . . . . . . . .

McCullough, J.; Hazen, Terry; Benson, Sally

1999-01-01T23:59:59.000Z

211

Methods of separating short half-life radionuclides from a mixture of radionuclides  

DOE Patents (OSTI)

The present invention is a method of obtaining a radionuclide product selected from the group consisting of {sup 223}Ra and {sup 225}Ac, from a radionuclide ``cow`` of {sup 227}Ac or {sup 229}Th respectively. The method comprises the steps of (a) permitting ingrowth of at least one radionuclide daughter from said radionuclide ``cow`` forming an ingrown mixture; (b) insuring that the ingrown mixture is a nitric acid ingrown mixture; (c) passing the nitric acid ingrown mixture through a first nitrate form ion exchange column which permits separating the ``cow`` from at least one radionuclide daughter; (d) insuring that the at least one radionuclide daughter contains the radionuclide product; (e) passing the at least one radionuclide daughter through a second ion exchange column and separating the at least one radionuclide daughter from the radionuclide product and (f) recycling the at least one radionuclide daughter by adding it to the ``cow``. In one embodiment the radionuclide ``cow`` is the {sup 227}Ac, the at least one daughter radionuclide is a {sup 227}Th and the product radionuclide is the {sup 223}Ra and the first nitrate form ion exchange column passes the {sup 227}Ac and retains the {sup 227}Th. In another embodiment the radionuclide ``cow`` is the {sup 229}Th, the at least one daughter radionuclide is a {sup 225}Ra and said product radionuclide is the {sup 225}Ac and the {sup 225}Ac and nitrate form ion exchange column retains the {sup 229}Th and passes the {sup 225}Ra/Ac. 8 figs.

Bray, L.A.; Ryan, J.L.

1998-09-15T23:59:59.000Z

212

Methods of separating short half-life radionuclides from a mixture of radionuclides  

DOE Patents (OSTI)

The present invention is a method of obtaining a radionuclide product selected from the group consisting of .sup.223 Ra and .sup.225 Ac, from a radionuclide "cow" of .sup.227 Ac or .sup.229 Th respectively. The method comprises the steps of a) permitting ingrowth of at least one radionuclide daughter from said radionuclide "cow" forming an ingrown mixture; b) insuring that the ingrown mixture is a nitric acid ingrown mixture; c) passing the nitric acid ingrown mixture through a first nitrate form ion exchange column which permits separating the "cow" from at least one radionuclide daughter; d) insuring that the at least one radionuclide daughter contains the radionuclide product; e) passing the at least one radionuclide daughter through a second ion exchange column and separating the at least one radionuclide daughter from the radionuclide product and f) recycling the at least one radionuclide daughter by adding it to the "cow". In one embodiment the radionuclide "cow" is the .sup.227 Ac, the at least one daughter radionuclide is a .sup.227 Th and the product radionuclide is the .sup.223 Ra and the first nitrate form ion exchange column passes the .sup.227 Ac and retains the .sup.227 Th. In another embodiment the radionuclide "cow"is the .sup.229 Th, the at least one daughter radionuclide is a .sup.225 Ra and said product radionuclide is the .sup.225 Ac and the .sup.225 Ac and nitrate form ion exchange column retains the .sup.229 Th and passes the .sup.225 Ra/Ac.

Bray, Lane A. (Richland, WA); Ryan, Jack L. (West Richland, WA)

1998-01-01T23:59:59.000Z

213

RECOVERY OF MERCURY FROM CONTAMINATED LIQUID WASTES  

SciTech Connect

Mercury was widely used in U.S. Department of Energy (DOE) weapons facilities, resulting in a broad range of mercury-contaminated wastes and wastewaters. Some of the mercury contamination has escaped to the local environment, particularly at the Y-12 Plant in Oak Ridge, Tennessee, where approximately 330 metric tons of mercury were discharged to the environment between 1953 and 1963 (TN & Associates, 1998). Effective removal of mercury contamination from water is a complex and difficult problem. In particular, mercury treatment of natural waters is difficult because of the low regulatory standards. For example, the Environmental Protection Agency has established a national ambient water quality standard of 12 parts-per-trillion (ppt), whereas the standard is 1.8 ppt in the Great Lakes Region. In addition, mercury in the environment is typically present in several different forms, but sorption processes are rarely effective with more than one or two of these forms. To meet the low regulatory discharge limits, an effective sorption process must be able to address all forms of mercury present in the water. One approach is to apply different sorbents in series depending on the mercury speciation and the regulatory discharge limits. ADA Technologies, Inc. has developed four new sorbents to address the variety of mercury species present in industrial discharges and natural waters. Three of these sorbents have been field tested on contaminated creek water at the Y-12 Plant. Two of these sorbents have been successfully demonstrated very high removal efficiencies for soluble mercury species, reducing mercury concentrations at the outlet of a pilot-scale system to less than 12 ppt for as long as six months. The other sorbent tested at the Y-12 Plant targeted colloidal mercury not removed by standard sorption or filtration processes. At the Y-12 Plant, colloidal mercury appears to be associated with iron, so a sorbent that removes mercury-iron complexes in the presence of a magnetic field was evaluated. Field results indicated good removal of this mercury fraction from the Y-12 waters. In addition, this sorbent is easily regenerated by simply removing the magnetic field and flushing the columns with water. The fourth sorbent is still undergoing laboratory development, but results to date indicate exceptionally high mercury sorption capacity. The sorbent is capable of removing all forms of mercury typically present in natural and industrial waters, including Hg{sup 2+}, elemental mercury, methyl mercury, and colloidal mercury. The process possesses very fast kinetics, which allows for higher flow rates and smaller treatment units. These sorbent technologies, used in tandem or individually depending on the treatment needs, can provide DOE sites with a cost-effective method for reducing mercury concentrations to very low levels mandated by the regulatory community. In addition, the technologies do not generate significant amounts of secondary wastes for disposal. Furthermore, the need for improved water treatment technologies is not unique to the DOE. The new, stringent requirements on mercury concentrations impact other government agencies as well as the private sector. Some of the private-sector industries needing improved methods for removing mercury from water include mining, chloralkali production, chemical processing, and medical waste treatment. The next logical step is to deploy one or more of these sorbents at a contaminated DOE site or at a commercial facility needing improved mercury treatment technologies. A full-scale deployment is planned in fiscal year 2000.

Robin M. Stewart

1999-09-29T23:59:59.000Z

214

A Mercury orientation model including non-zero obliquity and librations  

E-Print Network (OSTI)

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

Margot, Jean-Luc

2009-01-01T23:59:59.000Z

215

Colloid labelled with radionuclide and method  

DOE Patents (OSTI)

This report discusses a ferric hydroxide colloid having an alpha- emitting radionuclide essentially on the outer surfaces and a method of forming same. The method includes oxidizing a ferrous hydroxide to ferric hydroxide in the presence of a preselected radionuclide to form a colloid having the radionuclide on the outer surface thereof, and thereafter washing the colloid, and suspending the washed colloid in a suitable solution. The labeled colloid is useful in cancer therapy and for the treatment of inflamed joints. 3 tabs.

Atcher, R.W.; Hines, J.J.

1989-05-30T23:59:59.000Z

216

Method of making colloid labeled with radionuclide  

DOE Patents (OSTI)

A ferric hydroxide colloid having an alpha-emitting radionuclide essentially on the outer surfaces and a method of forming same. The method includes oxidizing a ferrous hydroxide to ferric hydroxide in the presence of a preselected radionuclide to form a colloid having the radionuclide on the outer surface thereof, and thereafter washing the colloid, and suspending the washed colloid in a suitable solution. The labelled colloid is useful in cancer therapy and for the treatment of inflamed joints.

Atcher, Robert W. (Chicago, IL); Hines, John J. (Glen Ellyn, IL)

1991-01-01T23:59:59.000Z

217

Colloid labelled with radionuclide and method  

DOE Patents (OSTI)

A ferric hydroxide colloid having an alpha-emitting radionuclide essentially on the outer surfaces and a method of forming same. The method includes oxidizing a ferrous hydroxide to ferric hydroxide in the presence of a preselected radionuclide to form a colloid having the radionuclide on the outer surface thereof, and thereafter washing the colloid, and suspending the washed colloid in a suitable solution. The labelled colloid is useful in cancer therapy and for the treatment of inflamed joints.

Atcher, Robert W. (Chicago, IL); Hines, John J. (GlenEllyn, IL)

1990-01-01T23:59:59.000Z

218

Measurement of radionuclides in waste packages  

DOE Patents (OSTI)

A method is described for non-destructively assaying the radionuclide content of solid waste in a sealed container by analysis of the waste's gamma-ray spectrum and neutron emissions. Some radionuclides are measured by characteristic photopeaks in the gamma-ray spectrum; transuranic nuclides are measured by neutron emission rate; other radionuclides are measured by correlation with those already measured.

Brodzinski, Ronald L. (Richland, WA); Perkins, Richard W. (Richland, WA); Rieck, Henry G. (Richland, WA); Wogman, Ned A. (Richland, WA)

1986-01-01T23:59:59.000Z

219

Colloid labelled with radionuclide and method  

DOE Patents (OSTI)

A ferric hydroxide colloid having an alpha-emitting radionuclide essentially on the outer surfaces and a method of forming same. The method includes oxidizing a ferrous hydroxide to ferric hydroxide in the presence of a preselected radionuclide to form a colloid having the radionuclide on the outer surface thereof, and thereafter washing the colloid, and suspending the washed colloid in a suitable solution. The labelled colloid is useful in cancer therapy and for the treatment of inflamed joints. No Drawings

Atcher, R.W.; Hines, J.J.

1990-11-13T23:59:59.000Z

220

Measurement of radionuclides in waste packages  

DOE Patents (OSTI)

A method is described for non-destructively assaying the radionuclide content of solid waste in a sealed container by analysis of the waste's gamma-ray spectrum and neutron emissions. Some radionuclides are measured by characteristic photopeaks in the gamma-ray spectrum; transuranic nuclides are measured by neutron emission rate; other radionuclides are measured by correlation with those already measured.

Brodzinski, R.L.; Perkins, R.W.; Rieck, H.G.; Wogman, N.A.

1984-09-12T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Design Strategies and Preliminary Prototype for a Low-Cost Arsenic...  

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

Researchers have invented a material called ARUBA - Arsenic Removal Using Bottom Ash - that effectively and affordably removes arsenic from Bangladesh groundwater. Through...

222

Mercury-Contaminated Hydraulic Mining Debris in San Francisco Bay  

E-Print Network (OSTI)

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

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

2010-01-01T23:59:59.000Z

223

Control of mercury methylation in wetlands through iron addition  

E-Print Network (OSTI)

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

Sedlak, David L; Ulrich, Patrick D

2009-01-01T23:59:59.000Z

224

Arsenic Removal from Groundwater Using Iron Electrocoagulation: Effect of  

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

Arsenic Removal from Groundwater Using Iron Electrocoagulation: Effect of Arsenic Removal from Groundwater Using Iron Electrocoagulation: Effect of Charge Dosage Rate Title Arsenic Removal from Groundwater Using Iron Electrocoagulation: Effect of Charge Dosage Rate Publication Type Journal Article Refereed Designation Refereed LBNL Report Number LBNL-6221E Year of Publication 2013 Authors Amrose, Susan, Ashok J. Gadgil, Venkat Srinivasan, Kristin Kowolik, Marc Muller, Jessica Huang, and Robert Kostecki Journal Joournal of Environmental Science and Health, Part A: Toxic/Hazardous Substances and Environmental Engineering Volume 48 Issue 9 Pagination 1019-1030 Date Published 04/2013 Keywords arsenic, bangladesh, Cambodia, dosage rate, electrocoagulation, india, water treatment Abstract We demonstrate that electrocoagulation (EC) using iron electrodes can reduce arsenic below 10 μg/L in synthetic Bangladesh groundwater and in real groundwater from Bangladesh and Cambodia while investigating the effect of operating parameters that are often overlooked, such as charge dosage rate. We measure arsenic removal performance

225

NIST Radionuclide Half-Life Measurements  

Science Conference Proceedings (OSTI)

... The half lives of many radionuclides have been measured in the Radioactivity Group of NIST. The table below, based on "New and revised half-life ...

2011-12-09T23:59:59.000Z

226

Ion binding compounds, radionuclide complexes, methods of making radionuclide complexes, methods of extracting radionuclides, and methods of delivering radionuclides to target locations  

DOE Patents (OSTI)

The invention pertains to compounds for binding lanthanide ions and actinide ions. The invention further pertains to compounds for binding radionuclides, and to methods of making radionuclide complexes. Also, the invention pertains to methods of extracting radionuclides. Additionally, the invention pertains to methods of delivering radionuclides to target locations. In one aspect, the invention includes a compound comprising: a) a calix[n]arene group, wherein n is an integer greater than 3, the calix[n]arene group comprising an upper rim and a lower rim; b) at least one ionizable group attached to the lower rim; and c) an ion selected from the group consisting of lanthanide and actinide elements bound to the ionizable group. In another aspect, the invention includes a method of extracting a radionuclide, comprising: a) providing a sample comprising a radionuclide; b) providing a calix[n]arene compound in contact with the sample, wherein n is an integer greater than 3; and c) extracting radionuclide from the sample into the calix[n]arene compound. In yet another aspect, the invention includes a method of delivering a radionuclide to a target location, comprising: a) providing a calix[n]arene compound, wherein n is an integer greater than 3, the calix[n]arene compound comprising at least one ionizable group; b) providing a radionuclide bound to the calix[n]arene compound; and c) providing an antibody attached to the calix[n]arene compound, the antibody being specific for a material found at the target location.

Chen, Xiaoyuan (Syracuse, NY); Wai, Chien M. (Moscow, ID); Fisher, Darrell R. (Richland, WA)

2000-01-01T23:59:59.000Z

227

Amended Silicated for Mercury Control  

Science Conference Proceedings (OSTI)

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

James Butz; Thomas Broderick; Craig Turchi

2006-12-31T23:59:59.000Z

228

COST OF MERCURY REMOVAL IN IGCC PLANTS  

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

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

229

Mercury in Alaskan Eskimo mothers and infants  

E-Print Network (OSTI)

The potential danger of natural mercury accumulation in the diet of the Eskimo is evaluated through mercury levels determined in cord blood, placenta, maternal blood, hair, and milk of 38 maternal-infant pairs from Anchorage and the Yukon-Kuskokwim Delta. Although mercury levels are not discernably dangerous, trends to larger accumulations in maternal and fetal RBC and placental tissue with proximity to the sea and consumption of seals during pregnancy provide the basis for considering possible indicators of neonatal involvement. Mercury level in RBC from cord blood appeared as the best potential indicator of this involvement, although relationships with the mother's diet and level of mercury in the placenta also appear useful. In this area, average and maximal mercury levels in cord blood are 39 and 78 ng/ml, respectively, far below the acknowledged toxic level in infants of these mothers who eat seals or fish every day during their pregnancy.

William A. Galster

1976-01-01T23:59:59.000Z

230

Mercury in the Lake Powell ecosystem  

SciTech Connect

Flameless atomic absorption analyses of samples from Lake Powell yield the following mercury levels (in mean parts per billion): 0.01 in lake water, 30 in bottom sediments, 10 in shoreline substrates, 34 in plant leaves, 145 in plant debris, 28 in algae, 10 in crayfish, and 232 in fish muscle. Bioamplification and the association of mercury with organic matter are evident in this recently created, relatively unpolluted reservoir. Formulation of an estimated mercury budget suggests that the restriction of outflow in the impounded Colorado River leads to mercury accumulation, and that projected regional coal-fired power generation may produce sufficient amounts of mercury to augment significantly the mercury released by natural weathering.

Standiford, D.R.; Potter, L.D.; Kidd, D.E.

1973-06-01T23:59:59.000Z

231

Assessment of Low Cost Novel Mercury Sorbents  

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

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

232

www.clu-in.org 1 Bioremediation of Arsenic, Chromium, Lead, and Mercury NOTICE  

E-Print Network (OSTI)

This document was prepared by Adebowale Adeniji, a National Network of Environmental Management studies grantee, under a fellowship from the U.S. Environmental Protection Agency. This report was not subject to EPA peer review or technical review. The EPA makes no warranties, expressed or implied, including without limitation, warranty for completeness, accuracy, or usefulness of the information, warranties as to the merchantability, or fitness for a particular purpose. Moreover, the listing of any technology, corporation, company, person, or facility in this report does not constitute endorsement, approval, or recommendation by the EPA. This report provides a basic orientation and current status of bioremediation for contaminants located in the subsurface. This report contains information gathered from a range of currently available sources, including project documents, reports, periodicals, Internet searches, and personal communication with involved parties. References for each case study are provided immediately following the case study. All sources are organized in alphabetical order at the end of the document. No attempts were made to independently confirm the resources used. It has been reproduced to help provide federal agencies, states, consulting engineering firms, private industries, and technology developers with information on the current status of this project. This paper addresses the status of the application of biological treatment to clean up hazardous metals from the earths subsurface (i.e., in situ bioremediation). The target audience includes federal and state regulators, planners, and site managers. The report is available on the Internet at www.clu-in.org/studentpapers/.

Adebowale Adeniji

2004-01-01T23:59:59.000Z

233

Emissions of air toxics from coal-fired boilers: Arsenic  

Science Conference Proceedings (OSTI)

Concerns over emissions of hazardous air pollutants (air toxics) have emerged as a major environmental issue; the authority of the US Environmental Protection Agency to regulate such pollutants has been greatly expanded through passage of the Clean Air Act Amendments of 1990. Arsenic and arsenic compounds are of concern mainly because of their generally recognized toxicity. Arsenic is also regarded as one of the trace elements in coal subject to significant vaporization. This report summarizes and evaluates available published information on the arsenic content of coals mined in the United States, on arsenic emitted in coal combustion, and on the efficacy of various environmental control technologies for controlling airborne emissions. Bituminous and lignite coals have the highest mean arsenic concentrations, with subbituminous and anthracite coals having the lowest. However, all coal types show very significant variations in arsenic concentrations. Arsenic emissions from coal combustion are not well-characterized, particularly with regard to determination of specific arsenic compounds. Variations in emission, rates of more than an order of magnitude have been reported for some boiler types. Data on the capture of arsenic by environmental control technologies are available primarily for systems with cold electrostatic precipitators, where removals of approximately 50 to 98% have been reported. Limited data for wet flue-gas-desulfurization systems show widely varying removals of from 6 to 97%. On the other hand, waste incineration plants report removals in a narrow range of from 95 to 99%. This report briefly reviews several areas of research that may lead to improvements in arsenic control for existing flue-gas-cleanup technologies and summarizes the status of analytical techniques for measuring arsenic emissions from combustion sources.

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

1994-08-01T23:59:59.000Z

234

Characterization and stabilization of arsenic in water treatment residuals  

E-Print Network (OSTI)

The characterization of water treatment residuals containing arsenic was investigated in the first study. Arsenic desorption and leachability from the residuals were the focus of this study. Arsenic leaching from water treatment residuals was found to be underestimated by the toxicity characteristic leaching test (TCLP) due to the pH of the leachates being favorable for As(V) adsorption. Competitive desorption of arsenic with phosphate was significant because phosphate tends to compete with As(V) on the surface of the metal hydroxide for adsorption sites. However, arsenic desorption by the competition of sulfate and chloride was found to be negligible. The pH in the leachate was a critical variable in controlling arsenic stability in the residuals. The release of arsenic from the residuals was elevated at low and high pH due to the increase dissolution of the adsorbents such as Fe and Al hydroxides. In the second phase of the study, the stabilization techniques for arsenic contained residuals and were examined to develop methods to suitably stabilize arsenic to eliminate and/or minimize leaching. A decrease of arsenic leaching was achieved by the addition of lime to the residuals and believed to be due to the formation of less soluble and stable calcium-arsenic compounds. However, it is suggested that the ordinary Portland cement (OPC) should be added with the lime for the long term stabilization because lime can be slowly consumed when directly exposed to atmospheric CO2. The solidification and stabilization (S/S) technique with lime and OPC was shown to be successfully applied by the immobilization of a wide variety of arsenic tainted water treatment residuals.

Wee, Hun Young

2003-08-01T23:59:59.000Z

235

Release of Mercury During Curing of Concrete Containing Fly Ash and Mercury Sorbent Material  

Science Conference Proceedings (OSTI)

This report provides laboratory data on mercury release during the initial curing stage of concrete made with fly ash or mixtures of fly ash and activated carbon containing mercury. These experiments suggest that mercury is not released from these concretes during initial curing.

2002-12-09T23:59:59.000Z

236

Process for removing mercury from aqueous solutions  

DOE Patents (OSTI)

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

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

1986-01-01T23:59:59.000Z

237

Process for removing mercury from aqueous solutions  

DOE Patents (OSTI)

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

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

1985-03-04T23:59:59.000Z

238

Remediation of Mercury and Industrial Contaminants Applied Field...  

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

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

239

NETL: Mercury Emissions Control Technologies - Non-Thermal Plasma...  

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

Non-Thermal Plasma Based Removal of Mercury Project Summary Powerspan Corp. will pilot test a multi-pollutant technology that converts mercury into mercuric oxide, nitrogen oxide...

240

Mercury Vapor At Desert Peak Area (Varekamp & Buseck, 1983) ...  

Open Energy Info (EERE)

Mercury Vapor At Desert Peak Area (Varekamp & Buseck, 1983) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Desert Peak Area...

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


241

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

Open Energy Info (EERE)

Mercury Vapor At Socorro Mountain Area (Kooten, 1987) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Socorro Mountain Area...

242

THE EFFECT OF MERCURY CONTROLS ON WALLBOARD MANUFACTURE  

Science Conference Proceedings (OSTI)

Pending EPA regulations may mandate 70 to 90% mercury removal efficiency from utility flue gas. A mercury control option is the trapping of oxidized mercury in wet flue gas desulfurization systems (FGD). The potential doubling of mercury in the FGD material and its effect on mercury volatility at temperatures common to wallboard manufacture is a concern that could limit the growing byproduct use of FGD material. Prediction of mercury fate is limited by lack of information on the mercury form in the FGD material. The parts per billion mercury concentrations prevent the identification of mercury compounds by common analytical methods. A sensitive analytical method, cold vapor atomic fluorescence, coupled with leaching and thermodecomposition methods were evaluated for their potential to identify mercury compounds in FGD material. The results of the study suggest that the mercury form is dominated by the calcium sulfate matrix and is probably associated with the sulfate form in the FGD material. Additionally, to determine the effect of high mercury concentration FGD material on wallboard manufacture, a laboratory FGD unit was built to trap the oxidized mercury generated in a simulated flue gas. Although the laboratory prepared FGD material did not contain the mercury concentrations anticipated, further thermal tests determined that mercury begins to evolve from FGD material at 380 to 390 F, consequently dropping the drying temperature should mitigate mercury evolution if necessary. Mercury evolution is also diminished as the weight of the wallboard sample increased. Consequently, mercury evolution may not be a significant problem in wallboard manufacture.

Sandra Meischen

2004-07-01T23:59:59.000Z

243

Mercury Vapor At Mccoy Geothermal Area (DOE GTP) | Open Energy...  

Open Energy Info (EERE)

Mercury Vapor At Mccoy Geothermal Area (DOE GTP) Exploration Activity Details Location Mccoy Geothermal Area Exploration Technique Mercury Vapor Activity Date Usefulness not...

244

NETL: Mercury Emissions Control Technologies - Demonstration...  

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

Demonstration of Integrated Approach to Mercury Control This project will demonstrate a novel multi-pollutant control technology for coal-fired power plants that can reduce...

245

NETL: IEP - Mercury Emissions Control: News Releases  

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

News Releases The following are links to various recent news stories related to mercury in the environment. These links are provided strictly as a convenience to the general...

246

NETL: Mercury Emissions Control Technologies - Brominated Sorbents...  

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

ESPs, and Fly Ash Use in Concrete Sorbent Technology will test two technologies for mercury removal from flue gas. Their concrete safe brominated sorbent will be tested at...

247

Apparatus for isotopic alteration of mercury vapor  

DOE Patents (OSTI)

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

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

1988-01-01T23:59:59.000Z

248

Mercury Emission Measurement at a CFB Plant  

DOE Green Energy (OSTI)

In response to pending regulation to control mercury emissions in the United States and Canada, several projects have been conducted to perform accurate mass balances at pulverized coal (pc)-fired utilities. Part of the mercury mass balance always includes total gaseous mercury as well as a determination of the speciation of the mercury emissions and a concentration bound to the particulate matter. This information then becomes useful in applying mercury control strategies, since the elemental mercury has traditionally been difficult to control by most technologies. In this instance, oxidation technologies have proven most beneficial for increased capture. Despite many years of mercury measurement and control projects at pc-fired units, far less work has been done on circulating fluidized-bed (CFB) units, which are able to combust a variety of feedstocks, including cofiring coal with biomass. Indeed, these units have proven to be more problematic because it is very difficult to obtain a reliable mercury mass balance. These units tend to have very different temperature profiles than pc-fired utility boilers. The flexibility of CFB units also tends to be an issue when a mercury balance is determined, since the mercury inputs to the system come from the bed material and a variety of fuels, which can have quite variable chemistry, especially for mercury. In addition, as an integral part of the CFB operation, the system employs a feedback loop to circulate the bed material through the combustor and the solids collection system (the primary cyclone), thereby subjecting particulate-bound metals to higher temperatures again. Despite these issues, CFB boilers generally emit very little mercury and show good native capture. The Energy & Environmental Research Center is carrying out this project for Metso Power in order to characterize the fate of mercury across the unit at Rosebud Plant, an industrial user of CFB technology from Metso. Appropriate solids were collected, and flue gas samples were obtained using the Ontario Hydro method, mercury continuous emission monitors, and sorbent trap methods. In addition, chlorine and fluorine were determined for solids and in the flue gas stream. Results of this project have indicated a very good mercury mass balance for Rosebud Plant, indicating 105 {+-} 19%, which is well within acceptable limits. The mercury flow through the system was shown to be primarily in with the coal and out with the flue gas, which falls outside of the norm for CFB boilers.

John Pavlish; Jeffrey Thompson; Lucinda Hamre

2009-02-28T23:59:59.000Z

249

Alkaline sorbent injection for mercury control  

DOE Patents (OSTI)

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

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

2003-01-01T23:59:59.000Z

250

Alkaline sorbent injection for mercury control  

DOE Patents (OSTI)

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

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

2002-01-01T23:59:59.000Z

251

Mercury concentrations in Maine sport fishes  

Science Conference Proceedings (OSTI)

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

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

1997-01-01T23:59:59.000Z

252

Establishing Measurement Traceability for Gaseous Mercury ...  

Science Conference Proceedings (OSTI)

... NIST already provides mercury traceability to the SI for many solid- and liquid-matrix materials, including fossil fuels, through the SRM program, but ...

2012-10-01T23:59:59.000Z

253

Mercury Sorbent Delivery System for Flue Gas  

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

(NETL) is seeking licensing partners interested in implementing United States Patent Number 7,494,632 entitled "Mercury Sorbent Delivery System for Flue Gas." Disclosed in...

254

NETL: Mercury Emissions Control Technologies - University of...  

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

Using SCR and SNCR NOx Control Technologies Determination of the Speciated Mercury Inventory at Four Coal-Fired Boilers Using Continuous Hg Monitors Longer-Term Testing of...

255

NETL: Mercury Emissions Control Technologies - Field Testing...  

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

or without performance additives, to reduce mercury emissions from a Texas utility burning either Texas lignite or a blend of Texas lignite and subbituminous coals. Sorbents...

256

NETL: Mercury Emissions Control Technologies - Modifications...  

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

Mercury Control Jointly funded by DOE and the Electric Power Research Institute (EPRI), this project's purpose is to investigate novel approaches of capturing elemental and...

257

Fate of Mercury in Wet FGD Systems  

Science Conference Proceedings (OSTI)

This report describes the results of a bench-scale, laboratory investigation of the fate of flue gas mercury species in wet flue gas desulfurization (FGD) scrubbers that are used for sulfur dioxide (SO2) control in coal-fired power plants. Data collected in the EPA mercury Information Collection Request (ICR), and in research projects sponsored by EPRI show that most wet scrubbers used for SO2 control achieve high removals of oxidized mercury and little or no elemental mercury removal. However, some scru...

2004-03-12T23:59:59.000Z

258

Mercury audit at Rocky Mountain Arsenal  

Science Conference Proceedings (OSTI)

This report presents the results of an environmental compliance audit to identify potential mercury-containing equipment in 261 building and 197 tanks at the Rocky Mountain Arsenal (RMA). The RMA, located near Denver, Colorado, is undergoing clean up and decommissioning by the Department of the Army. Part of the decommissioning procedure is to ensure that all hazardous wastes are properly identified and disposed of. The purpose of the audit was to identify any mercury spills and mercury-containing instrumentation. The audit were conducted from April 7, 1992, through July 16, 1992, by a two-person team. The team interviewed personnel with knowledge of past uses of the buildings and tanks. Information concerning past mercury spills and the locations and types of instrumentation that contain mercury proved to be invaluable for an accurate survey of the arsenal. The team used a Jerome{reg_sign} 431-X{trademark} Mercury Vapor Analyzer to detect spills and confirm locations of mercury vapor. Twelve detections were recorded during the audit and varied from visible mercury spills to slightly elevated readings in the corners of rooms with past spills. The audit also identified instrumentation that contained mercury. All data have been incorporated into a computerized data base that is compatible with the RMA data base.

Smith, S.M.; Jensen, M.K. [Oak Ridge National Lab., TN (United States); Anderson, G.M. [Rocky Mountain Arsenal, Denver, CO (United States)

1994-02-01T23:59:59.000Z

259

Life Redefined: Microbes Built with Arsenic  

DOE Green Energy (OSTI)

Life can survive in many harsh environments, from extreme heat to the presence of deadly chemicals. However, life as we know it has always been based on the same six elements -- carbon, oxygen, nitrogen, hydrogen, sulfur and phosphorus. Now it appears that even this rule has an exception. In the saline and poisonous environment of Mono Lake, researchers have found a bacterium that can grow by incorporating arsenic into its structure in place of phosphorus. X-ray images taken at SLAC's synchrotron light source reveal that this microbe may even use arsenic as a building block for DNA. Please join us as we describe this discovery, which rewrites the textbook description of how living cells work.

Webb, Sam (SLAC and Felisa Wolfe-Simon, NASA and U.S. Geological Survey)

2011-03-22T23:59:59.000Z

260

Removal of arsenic compounds from petroliferous liquids  

DOE Patents (OSTI)

Described is a process for removing arsenic from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic bound to it from contacting petroliferous liquid as described above and involves: a. treating said spent catecholated polystyrene, at a temperature in the range of about 20.degree. to 100.degree. C. with an aqueous solution of at least one carbonate and/or bicarbonate of ammonium, alkali and alkaline earth metals, said solution having a pH between about 8 and 10 and, b. separating the solids and liquids from each other. Preferably the regeneration treatment is in two steps wherein step (a) is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, steps (a) and (b) are repeated using a bicarbonate.

Fish, Richard H. (Berkeley, CA)

1985-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Controls on Fluxes of Mercury in Aquatic Food Webs: Application of the Dynamic Mercury Cycling Model to Four Enclosure Experiments w ith Additions of Stable Mercury Isotopes  

Science Conference Proceedings (OSTI)

New controls on utility mercury emissions are under consideration in order to limit human exposure to mercury resulting from fish consumption. Evaluation of such measures requires an understanding of how mercury cycles through lakes and streams. This report describes the application of EPRI's Dynamic Mercury Cycling Model (D-MCM) to experiments involving the addition of stable mercury Hg(II) isotopes to four 10-meter-diameter enclosures in a lake.

2001-09-21T23:59:59.000Z

262

Oak Ridge Moves Forward in Mercury Cleanup | Department of Energy  

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

Oak Ridge Moves Forward in Mercury Cleanup Oak Ridge Moves Forward in Mercury Cleanup Oak Ridge Moves Forward in Mercury Cleanup March 28, 2013 - 12:00pm Addthis Workers recently removed five large mercury-contaminated tanks from Y-12. Workers recently removed five large mercury-contaminated tanks from Y-12. Removing these tanks is part of the steps to reduce potential risk from mercury at Y-12. Removing these tanks is part of the steps to reduce potential risk from mercury at Y-12. Workers recently removed five large mercury-contaminated tanks from Y-12. Removing these tanks is part of the steps to reduce potential risk from mercury at Y-12. OAK RIDGE, Tenn. - Oak Ridge's EM program is making significant progress to reduce environmental mercury releases from the Y-12 National Security Complex. Mercury is one of the greatest environmental concerns facing the Oak Ridge

263

Oak Ridge Moves Forward in Mercury Cleanup | Department of Energy  

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

Moves Forward in Mercury Cleanup Moves Forward in Mercury Cleanup Oak Ridge Moves Forward in Mercury Cleanup March 28, 2013 - 12:00pm Addthis Workers recently removed five large mercury-contaminated tanks from Y-12. Workers recently removed five large mercury-contaminated tanks from Y-12. Removing these tanks is part of the steps to reduce potential risk from mercury at Y-12. Removing these tanks is part of the steps to reduce potential risk from mercury at Y-12. Workers recently removed five large mercury-contaminated tanks from Y-12. Removing these tanks is part of the steps to reduce potential risk from mercury at Y-12. OAK RIDGE, Tenn. - Oak Ridge's EM program is making significant progress to reduce environmental mercury releases from the Y-12 National Security Complex. Mercury is one of the greatest environmental concerns facing the Oak Ridge

264

Mercury: the planet and its orbit  

E-Print Network (OSTI)

The planet closest to the Sun, Mercury, is the subject of renewed attention among planetary scientists, as two major space missions will visit it within the next decade. These will be the first to return to Mercury, after the flybys by NASA's Mariner 10 spacecraft in 1974--5. The difficulties of observing this planet from the Earth make such missions necessary for further progress in understanding its origin, evolution and present state. This review provides an overview of what is known about Mercury and what are the major outstanding issues. Mercury's orbital and rotation periods are in a unique 2:3 resonance; an analysis of the orbital dynamics of Mercury is presented here, as well as Mercury's special role in testing theories of gravitation. These derivations provide a good insight into the complexities of planetary motion in general, and how, in the case of Mercury, its proximity to the Sun can be described and exploited in terms of general relativity. Mercury's surface, superficially similar to that of the Moon, presents intriguing differences, representing a different, and more complex history in which the role of early volcanism remains to be clarified and understood. Mercury's interior presents the most important puzzles: it has the highest uncompressed density among the terrestrial planets, implying a very large, mostly iron core. This does not appear to be the completely solidified yet, as Mariner 10 found a planetary magnetic field that is probably generated by an internal dynamo, in a liquid outer layer of the large iron core. The current state of the core, once established, will provide a constraint for its evolution from the time of the planet's formation. Mercury's environment is highly variable. There is only a tenuous exosphere around Mercury; its sourc...

Andr Balogh; Giacomo Giampieri

2002-01-01T23:59:59.000Z

265

Recovery of Mercury From Contaminated Liquid Wastes  

SciTech Connect

The Base Contract program emphasized the manufacture and testing of superior sorbents for mercury removal, testing of the sorption process at a DOE site, and determination of the regeneration conditions in the laboratory. During this project, ADA Technologies, Inc. demonstrated the following key elements of a successful regenerable mercury sorption process: (1) sorbents that have a high capacity for dissolved, ionic mercury; (2) removal of ionic mercury at greater than 99% efficiency; and (3) thermal regeneration of the spent sorbent. ADA's process is based on the highly efficient and selective sorption of mercury by noble metals. Contaminated liquid flows through two packed columns that contain microporous sorbent particles on which a noble metal has been finely dispersed. A third column is held in reserve. When the sorbent is loaded with mercury to the point of breakthrough at the outlet of the second column, the first column is taken off-line and the flow of contaminated liquid is switched to the second and third columns. The spent column is regenerated by heating. A small flow of purge gas carries the desorbed mercury to a capture unit where the liquid mercury is recovered. Laboratory-scale tests with mercuric chloride solutions demonstrated the sorbents' ability to remove mercury from contaminated wastewater. Isotherms on surrogate wastes from DOE's Y-12 Plant in Oak Ridge, Tennessee showed greater than 99.9% mercury removal. Laboratory- and pilot-scale tests on actual Y-12 Plant wastes were also successful. Mercury concentrations were reduced to less than 1 ppt from a starting concentration of 1,000 ppt. The treatment objective was 50 ppt. The sorption unit showed 10 ppt discharge after six months. Laboratory-scale tests demonstrated the feasibility of sorbent regeneration. Results show that sorption behavior is not affected after four cycles.

1998-06-12T23:59:59.000Z

266

Fly ash properties and mercury sorbent affect mercury release from curing concrete  

Science Conference Proceedings (OSTI)

The release of mercury from concrete containing fly ashes from various generator boilers and powdered activated carbon sorbent used to capture mercury was measured in laboratory experiments. Release of gaseous mercury from these concretes was less than 0.31% of the total quantity of mercury present. The observed gaseous emissions of mercury during the curing process demonstrated a dependency on the organic carbon content of the fly ash, with mercury release decreasing with increasing carbon content. Further, lower gaseous emissions of mercury were observed for concretes incorporating ash containing activated carbon sorbent than would be expected based on the observed association with organic carbon, suggesting that the powdered activated carbon more tightly binds the mercury as compared to unburned carbon in the ash. Following the initial 28-day curing interval, mercury release diminished with time. In separate leaching experiments, average mercury concentrations leached from fly ash concretes were less than 4.1 ng/L after 18 h and 7 days, demonstrating that less than 0.02% of the mercury was released during leaching. 25 refs., 4 figs., 5 tabs.

Danold W. Golightly; Chin-Min Cheng; Linda K. Weavers; Harold W. Walker; William E. Wolfe [State University, Columbus, OH (United States). Department of Civil and Environmental Engineering and Geodetic Science

2009-04-15T23:59:59.000Z

267

2006 Mercury Control Technology Conference Proceedings  

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

Mercury Control Technology Conference Mercury Control Technology Conference December 11-13, 2006 Table of Contents Disclaimer Papers and Presentations Introduction Sorbent Injection By-Product Characterization/Management Mercury Oxidation and Co-Removal with FGD Systems Other Mercury Control Technology Panel Discussions Posters New 2006 Phase III Mercury Field Testing Projects Sorbent Injection Pretreatment of Coal Oxidation of Mercury Environmental Studies on Mercury Mercury in CUBs Disclaimer This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government or any agency thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise does not necessarily constitute or imply its endorsement, recommendation, or favoring by the United States Government or any agency thereof. The views and opinions of authors expressed herein do not necessarily state or reflect those of the United States Government or any agency thereof.

268

Transverse section radionuclide scanning system  

DOE Patents (OSTI)

This invention provides a transverse section radionuclide scanning system for high-sensitivity quantification of brain radioactivity in cross-section picture format in order to permit accurate assessment of regional brain function localized in three-dimensions. High sensitivity crucially depends on overcoming the heretofore known raster type scanning, which requires back and forth detector movement involving dead-time or partial enclosure of the scan field. Accordingly, this invention provides a detector array having no back and forth movement by interlaced detectors that enclose the scan field and rotate as an integral unit around one axis of rotation in a slip ring that continuously transmits the detector data by means of laser emitting diodes, with the advantages that increased amounts of data can be continuously collected, processed and displayed with increased sensitivity according to a suitable computer program.

Kuhl, David E. (Rosemont, PA); Edwards, Roy Q. (Plymouth Township, PA)

1976-01-01T23:59:59.000Z

269

Arsenic Health and Ecological Effects: Soil and Water  

Science Conference Proceedings (OSTI)

Arsenic is a naturally occurring element found throughout the environment in many different forms. It is also found in coal and thus coal combustion products and can be associated with other power plant generation and delivery operations. This report summarizes information on the toxicity of arsenic in the environment and derives risk factors based on this information.

2007-09-17T23:59:59.000Z

270

In situ chemical fixation of arsenic-contaminated soils: An experimental study  

E-Print Network (OSTI)

arsenic trioxide with a trade name Anaconda fromformer Anaconda smelter as a major ingredient during the

Yang, Li; Donahoe, Rona J.; Redwine, James C.

2007-01-01T23:59:59.000Z

271

Milestone Project Demonstrates Innovative Mercury Emissions Reduction  

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

Milestone Project Demonstrates Innovative Mercury Emissions Milestone Project Demonstrates Innovative Mercury Emissions Reduction Technology Milestone Project Demonstrates Innovative Mercury Emissions Reduction Technology January 12, 2010 - 12:00pm Addthis Washington, DC - An innovative technology that could potentially help some coal-based power generation facilities comply with anticipated new mercury emissions standards was successfully demonstrated in a recently concluded milestone project at a Michigan power plant. Under a cooperative agreement with the U.S. Department of Energy's (DOE's) National Energy Technology Laboratory (NETL), WE Energies demonstrated the TOXECON(TM) process in a $52.9million project at the Presque Isle Power Plant in Marquette, Mich. TOXECON is a relatively cost-effective option for achieving significant reductions in mercury emissions and increasing the

272

Mercury removal from solid mixed waste  

SciTech Connect

The removal of mercury from mixed wastes is an essential step in eliminating the temporary storage of large inventories of mixed waste throughout the Department of Energy (DOE) complex. Currently thermal treatment has been identified as a baseline technology and is being developed as part of the DOE Mixed Waste Integrated Program (MWIP). Since thermal treatment will not be applicable to all mercury containing mixed waste and the removal of mercury prior to thermal treatment may be desirable, laboratory studies have been initiated at Oak Ridge National Laboratory (ORNL) to develop alternative remediation technologies capable of removing mercury from certain mixed waste. This paper describes laboratory investigations of the KI/I{sub 2} leaching processes to determine the applicability of this process to mercury containing solid mixed waste.

Gates, D.D.; Morrissey, M.; Chava, K.K.; Chao, K.

1994-12-31T23:59:59.000Z

273

Mercury Emissions Control in Wet FGD Systems  

E-Print Network (OSTI)

The Babcock & Wilcox Company (B&W) and McDermott Technology, Inc. (MTI) have had a continuing program over the past decade for characterizing and optimizing mercury control in flue gas desulfurization (FGD) systems. These efforts have led to the characterization of mercury emissions control at two utility installations and full-scale demonstration (55 MW and 1300 MW) of the effect of a mercury control performance enhancement additive for wet FGD systems. This paper presents the results of the mercury emissions control testing conducted at these two sites. The performance is related to EPA Information Collection Request (ICR) data from an FGD system suppliers perspective, highlighting the need to consider the effects of system design and operation when evaluating mercury emissions control performance.

Paul S. Nolan; Babcock Wilcox; Kevin E. Redinger; Babcock Wilcox; Gerald T. Amrhein; Gregory A. Kudlac

2002-01-01T23:59:59.000Z

274

Arsenic Removal by Photochemical Methods: Nanoparticulate Zerovalent Iron  

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

Arsenic Removal by Photochemical Methods: Nanoparticulate Zerovalent Iron Arsenic Removal by Photochemical Methods: Nanoparticulate Zerovalent Iron and Heterogeneous Photocatalysis with TiO2 Speaker(s): Marta Litter Date: November 19, 2010 - 11:00am Location: 90-3122 Seminar Host/Point of Contact: Hugo Destaillats Arsenic in groundwater is a dramatic global problem due to the high incidence of arsenicosis or HACRE (Chronic Endemic Regional Hydro-arsenicism, Hidroarsenicismo Crónico Regional Endémico in Spanish), a severe illness causing skin lesions and cancer in extended regions of the world. For this reason, research on low-cost technologies for As removal to be applied in isolated, poor, rural locations is mandatory. This seminar will present a brief overview of arsenic pollution issues and mitigation needs in Latin America. It will also present results on As(V) removal using

275

Assessing the Risk of Arsenic Ingestion | Advanced Photon Source  

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

An Electronic Dance of Spins and Orbits An Electronic Dance of Spins and Orbits How a Virus Prepares to Infect Cells Magnetic Switching under Pressure Revealing the Secrets of Chemical Bath Deposition DNA Repair Protein Caught in the Act of Molecular Theft Science Highlights Archives: 2013 | 2012 | 2011 | 2010 2009 | 2008 | 2007 | 2006 2005 | 2004 | 2003 | 2002 2001 | 2000 | 1998 | Subscribe to APS Science Highlights rss feed Assessing the Risk of Arsenic Ingestion DECEMBER 17, 2010 Bookmark and Share Mineralogy, percent arsenic bioaccessibility and total arsenic concentration of samples from Nova Scotia mine tailings. Detailed mineralogical analyses of individual samples revealed up to seven arsenic species in individual samples (six shown here as major arsenic phases). Results of a physiologically based extraction test are for the < 150 µm

276

IMPACT OF ELIMINATING MERCURY REMOVAL PRETREATMENT ON THE PERFORMANCE OF A HIGH LEVEL RADIOACTIVE WASTE MELTER OFFGAS SYSTEM  

DOE Green Energy (OSTI)

The Defense Waste Processing Facility at the Savannah River Site processes high-level radioactive waste from the processing of nuclear materials that contains dissolved and precipitated metals and radionuclides. Vitrification of this waste into borosilicate glass for ultimate disposal at a geologic repository involves chemically modifying the waste to make it compatible with the glass melter system. Pretreatment steps include removal of excess aluminum by dissolution and washing, and processing with formic and nitric acids to: (1) adjust the reduction-oxidation (redox) potential in the glass melter to reduce radionuclide volatility and improve melt rate; (2) adjust feed rheology; and (3) reduce by steam stripping the amount of mercury that must be processed in the melter. Elimination of formic acid pretreatment has been proposed to eliminate the production of hydrogen in the pretreatment systems; alternative reductants would be used to control redox. However, elimination of formic acid would result in significantly more mercury in the melter feed; the current specification is no more than 0.45 wt%, while the maximum expected prior to pretreatment is about 2.5 wt%. An engineering study has been undertaken to estimate the effects of eliminating mercury removal on the melter offgas system performance. A homogeneous gas-phase oxidation model and an aqueous phase model were developed to study the speciation of mercury in the DWPF melter offgas system. The model was calibrated against available experimental data and then applied to DWPF conditions. The gas-phase model predicted the Hg{sub 2}{sup 2-}/Hg{sup 2+} ratio accurately, but some un-oxidized Hg{sup 0} remained. The aqueous model, with the addition of less than 1 mM Cl{sub 2} showed that this remaining Hg{sup 0} would be oxidized such that the final Hg{sub 2}{sup 2+}/Hg{sup 2+} ratios matched the experimental data. The results of applying the model to DWPF show that due to excessive shortage of chloride, only 6% of the mercury fed is expected to be chlorinated, mostly as Hg{sub 2}Cl{sub 2}, while the remaining mercury would exist either as elemental mercury (90%) or HgO (4%).

Zamecnik, J; Alexander Choi, A

2009-03-17T23:59:59.000Z

277

Developments in Bioremediation of Soils and Sediments Polluted with Metals and Radionuclides: 2. Field Research on Bioremediation of Metals and Radionuclides  

E-Print Network (OSTI)

of metals and radionuclides shows great promise but it willand Sediments Polluted with Metals and Radionuclides 2.Bioremediation of Metals and Radionuclides Terry C. Hazen 1

Hazen, Terry C.

2010-01-01T23:59:59.000Z

278

Analysis of mercury diffusion pumps  

SciTech Connect

Several mercury diffusion pump stages in the Tritium Purification process at the Savannah River Site (SRS) have been removed from service for scheduled preventive maintenance. These stages have been examined to determine if failure has occurred. Evidence of fatigue around the flange portion of the pump has been seen. In addition, erosion and cavitation inside the throat of the venturi tube and corrosion on the other surface of the venturi tube has been observed. Several measures are being examined in an attempt to improve the performance of these pumps. These measures, as well as the noted observations, are described. 4 refs.

Dunn, K.A.

1991-12-31T23:59:59.000Z

279

Analysis of mercury diffusion pumps  

SciTech Connect

Several mercury diffusion pump stages in the Tritium Purification process at the Savannah River Site (SRS) have been removed from service for scheduled preventive maintenance. These stages have been examined to determine if failure has occurred. Evidence of fatigue around the flange portion of the pump has been seen. In addition, erosion and cavitation inside the throat of the venturi tube and corrosion on the other surface of the venturi tube has been observed. Several measures are being examined in an attempt to improve the performance of these pumps. These measures, as well as the noted observations, are described. 4 refs.

Dunn, K.A.

1991-01-01T23:59:59.000Z

280

Treatment of mercury containing waste  

DOE Patents (OSTI)

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

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

2002-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Geothermal Exploration Using Surface Mercury Geochemistry | Open Energy  

Open Energy Info (EERE)

Surface Mercury Geochemistry Surface Mercury Geochemistry Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Journal Article: Geothermal Exploration Using Surface Mercury Geochemistry Details Activities (5) Areas (3) Regions (0) Abstract: Shallow, soil-mercury surveys can be used effectively in exploration for geothermal resources. Soil-mercury data from six areas in Nevada, California and New Mexico are analyzed using contour maps, histogram and probability graphs. Plotting on probability graphs allows background and anomalous populations to be resolved even when considerable overlap between populations is present. As is shown in several examples, separate soil-mercury populations can be plausibly interpreted. Mercury data can significantly enhance the structural understanding of a prospect

282

2008 LANL radionuclide air emissions report  

SciTech Connect

The emissions of radionuclides from Department of Energy Facilities such as Los Alamos National Laboratory (LANL) are regulated by the Amendments to the Clean Air Act of 1990, National Emissions Standards for Hazardous Air Pollutants (40 CFR 61 Subpart H). These regulations established an annual dose limit of 10 mrem to the maximally exposed member of the public attributable to emissions of radionuclides. This document describes the emissions of radionuclides from LANL and the dose calculations resulting from these emissions for calendar year 2008. This report meets the reporting requirements established in the regulations.

Fuehne, David P.

2009-06-01T23:59:59.000Z

283

2010 LANL radionuclide air emissions report /  

SciTech Connect

The emissions of radionuclides from Department of Energy Facilities such as Los Alamos National Laboratory (LANL) are regulated by the Amendments to the Clean Air Act of 1990, National Emissions Standards for Hazardous Air Pollutants (40 CFR 61 Subpart H). These regulations established an annual dose limit of 10 mrem to the maximally exposed member of the public attributable to emissions of radionuclides. This document describes the emissions of radionuclides from LANL and the dose calculations resulting from these emissions for calendar year 2010. This report meets the reporting requirements established in the regulations.

Fuehne, David P.

2011-06-01T23:59:59.000Z

284

Selective extraction of copper, mercury, silver and palladium ions from water using hydrophobic ionic liquids.  

E-Print Network (OSTI)

K. ; Khan, R. H. Low dose mercury toxicity and human health.Gochfeld, M. Cases of mercury exposure, bioavailability, andto enhanced extraction for mercury. Acknowledgements For

Papaiconomou, Nicolas; Lee, Jong-Min; Salminen, Justin; Von Stosch, Moritz; Prausnitz, John M.

2008-01-01T23:59:59.000Z

285

A Mass Balance for Mercury in the San Francisco Bay Area  

E-Print Network (OSTI)

and transformation of mercury. I. Model development andand transformation of mercury. II. Simulation results forFernandez, G. C. J. , Mercury and plants in contaminated

MacLeod, Matthew; McKone, Thomas E.; Mackay, Don

2005-01-01T23:59:59.000Z

286

Guidelines for Mercury Measurements Using the Ontario Hydro Method  

Science Conference Proceedings (OSTI)

The Clean Air Mercury Rule (CAMR) requires measurement of mercury emissions from coal-fired power plants. The rule requires that all coal-fired power plants emitting >29 lb of mercury per year install continuous mercury measurement technology. Either a continuous mercury monitor (CMM) or sorbent traps meeting the requirements of 40 Code of Federal Regulations (CFR) Part 75, Appendix K, protocols must be used. To ensure the technologies are operating properly, CAMR also requires that a relative accuracy t...

2007-08-28T23:59:59.000Z

287

Development of Mercury Oxidation Catalyst for Enhanced Mercury Capture by Wet FGD  

Science Conference Proceedings (OSTI)

This document describes recent progress on a mercury control technology development program co-funded by EPRI, the U.S. Department of Energys National Energy Technology Laboratory (DOE-NETL), and several EPRI-member companies. The mercury control process under development uses catalysts installed downstream of the air heater and particulate control device to promote the oxidation of elemental mercury in flue gas from coal-fired power plants that have wet lime or limestone flue gas desulfurization (FGD) ...

2007-03-13T23:59:59.000Z

288

AN EXPERIMENT ON DEHASIDDHI WITH MERCURY  

E-Print Network (OSTI)

ABSTRACT: The author experimented with the dehasiddhi using mercury. The interesting experiment is narrated in this article. The land of Bharath is the only place which developed the science dealing with the metal remedies for holistic health during the Vedic period when people in other parts of the world continued to use potions and witchcraft to cure diseases of the body. This science in Vedic language is termed rasa sastra. It uses metals such as iron, copper, silver, gold mercury, elements such as iron, copper, silver, gold mercury, elements such as sulphur, mica and other materials such as shells, pearls corals jewels, salts, etc in a purified and processed form for internal

M. P Alexander

1995-01-01T23:59:59.000Z

289

Arsenic exposure in children living near a former copper smelter  

SciTech Connect

About 10,000 people live in communities surrounding the former copper smelter at Anaconda, Montana. Most of these people live in the town of Anaconda, which is generally upwind of the smelter. The smelter ceased operations in 1980, after almost a century of ore processing. Soil and dust on the smelter site and in the vicinity remain contaminated with arsenic, although at this time air and drinking water arsenic levels are not elevated. Results of soil and dust sampling for arsenic in the communities around the smelter are reported. In the town of Anaconda, surface soil arsenic levels from residential sites have averaged around 100 ppm or greater. Young children are generally believed to be the population with the most nonoccupational exposure to soil. Several models of exposure to environmental arsenic in the Anaconda area have predicted that children living in all communities surrounding the smelter would be having significant and measurable exposure to arsenic. Two exposures surveys, conducted while the smelter was operative, demonstrated that excess exposure to arsenic was occurring in young children. Until the present surveys, no exposure data had been collected since the smelter was closed.

Binder, S.; Forney, D.; Kaye, W.; Paschal, D.

1987-07-01T23:59:59.000Z

290

Arsenic in drinking water and lung cancer: A systematic review  

SciTech Connect

Exposure to inorganic arsenic via drinking water is a growing public health concern. We conducted a systematic review of the literature examining the association between arsenic in drinking water and the risk of lung cancer in humans. Towards this aim, we searched electronic databases for articles published through April 2006. Nine ecological studies, two case-control studies, and six cohort studies were identified. The majority of the studies were conducted in areas of high arsenic exposure (100 {mu}g/L) such as southwestern Taiwan, the Niigata Prefecture, Japan, and Northern Chile. Most of the studies reported markedly higher risks of lung cancer mortality or incidence in high arsenic areas compared to the general population or a low arsenic exposed reference group. The quality assessment showed that, among the studies identified, only four assessed arsenic exposure at the individual level. Further, only one of the ecological studies presented results adjusted for potential confounders other than age; of the cohort and case-control studies, only one-half adjusted for cigarette smoking status in the analysis. Despite these methodologic limitations, the consistent observation of strong, statistically significant associations from different study designs carried out in different regions provide support for a causal association between ingesting drinking water with high concentrations of arsenic and lung cancer. The lung cancer risk at lower exposure concentrations remains uncertain.

Celik, Ismail [Department of Medical Oncology, Hacettepe University Institute of Oncology, Ankara (Turkey); Gallicchio, Lisa [Prevention and Research Center, Mercy Medical Center (United States); Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health (United States); Boyd, Kristina; Lam, Tram K.; Matanoski, Genevieve [Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health (United States); Tao Xuguang [Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health (United States); Department of Occupational and Environmental Medicine, Johns Hopkins University School of Medicine (United States); Shiels, Meredith; Hammond, Edward [Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health (United States); Chen Liwei [Department of International Health, Center for Human Nutrition, Johns Hopkins University Bloomberg School of Public Health (United States); Robinson, Karen A. [Department of General Internal Medicine, Johns Hopkins University School of Medicine (United States); Caulfield, Laura E. [Department of International Health, Center for Human Nutrition, Johns Hopkins University Bloomberg School of Public Health (United States); Herman, James G. [Department of Oncology, Johns Hopkins University School of Medicine (United States); Guallar, Eliseo [Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health (United States); Alberg, Anthony J. [Department of Epidemiology, Johns Hopkins University Bloomberg School of Public Health (United States); Cancer Prevention and Control Program, Hollings Cancer Center, and Department of Biostatistics, Bioinformatics and Epidemiology, Medical University of South Carolina (United States)], E-mail: alberg@musc.edu

2008-09-15T23:59:59.000Z

291

Removing Arsenic from Contaminated Drinking Water in Rural Bangladesh:  

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

Removing Arsenic from Contaminated Drinking Water in Rural Bangladesh: Removing Arsenic from Contaminated Drinking Water in Rural Bangladesh: Recent Fieldwork Results & Policy Implications Title Removing Arsenic from Contaminated Drinking Water in Rural Bangladesh: Recent Fieldwork Results & Policy Implications Publication Type Report Year of Publication 2009 Authors Mathieu, Johanna L., Ashok J. Gadgil, Kristin Kowolik, and Susan E. Addy Publisher Lawrence Berkeley National Laboratory City Berkeley Abstract of arsenic from drinking water in Bangladesh. During fieldwork in four sub-districts of the country, ARUBA reduced arsenic levels ranging from 200 to 900 ppb to below the Bangladesh standard of 50 ppb. The technology is cost-effective because the substrate-bottom ash from coal fired power plants-is a waste material readily available in South Asia. In comparison to similar technologies, ARUBA uses less media for arsenic removal due to its high surface area to volume ratio. Hence, less waste is produced. A number of experiments were conducted in Bangladesh to determine the effectiveness of various water treatment protocols. It was found that (1) ARUBA removes more thanhalf of the arsenic from water within five minutes of treatment, (2) ARUBA, that has settled at the bottom of a treatment vessel, continues to remove arsenic for 2-3 days, (3) ARUBA's arsenic removal efficiency can be improved through sequential partial dosing (adding a given amount of ARUBA in fractions versus all at once), and (4) allowing water to first stand for two to three days followed by treatment with ARUBA produced final arsenic levels ten times lower than treating water directly out of the well. Our findings imply a number of tradeoffs between ARUBA's effective arsenic removal capacity, treatment system costs, and waste output. These tradeoffs, some a function of arsenic-related policies in Bangladesh (e.g., waste disposal regulations), must be considered when designing anarsenic removal system. We propose that the most attractive option is to use ARUBA in communityscale water treatment centers, installed as public-private partnerships, in Bangladeshi villages

292

Removal of arsenic compounds from petroliferous liquids  

DOE Patents (OSTI)

The present invention in one aspect comprises a process for removing arsenic from petroliferous-derived liquids by contacting said liquid with a divinylbenzene-crosslinked polystyrene polymer (i.e. PS-DVB) having catechol ligands anchored to said polymer, said contacting being at an elevated temperature. In another aspect, the invention is a process for regenerating spent catecholated polystyrene polymer by removal of the arsenic bound to it from contacting petroliferous liquid in accordance with the aspect described above which regenerating process comprises: (a) treating said spent catecholated polystyrene polymer with an aqueous solution of at least one member selected from the group consisting of carbonates and bicarbonates of ammonium, alkali metals, and alkaline earth metals, said solution having a pH between about 8 and 10, and said treating being at a temperature in the range of about 20/sup 0/ to 100/sup 0/C; (b) separating the solids and liquids from each other. In a preferred embodiment the regeneration treatment is in two steps wherein step: (a) is carried out with an aqueous alcoholic carbonate solution which includes at least one lower alkyl alcohol, and, steps (c) and (d) are added. Steps (c) and (d) comprise: (c) treating the solids with an aqueous alcoholic solution of at least one ammonium, alkali or alkaline earth metal bicarbonate at a temperature in the range of about 20 to 100/sup 0/C; and (d) separating the solids from the liquids.

Fish, R.H.

1984-04-06T23:59:59.000Z

293

Mercury cleanup efforts intensify | Y-12 National Security Complex  

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

Mercury cleanup efforts ... Mercury cleanup efforts ... Mercury cleanup efforts intensify Posted: February 11, 2013 - 3:31pm | Y-12 Report | Volume 9, Issue 2 | 2013 Millions of pounds of mercury were required to support Y-12's post-World War II mission of separating lithium isotopes. Cleaning up the toxic heavy metal poses many challenges, but what Y-12 is learning could help conquer mercury pollution worldwide. There's a reason you won't find mercury in many thermometers these days. Mercury is a heavy metal that occurs in several chemical forms, all of which can produce toxic effects in high enough doses. Mercury was used in the column exchange process, which Y-12 employed to produce lithium-6 from 1953 to 1962. Through process spills, system leaks and surface runoff, some 700,000 pounds of mercury have been lost to the

294

NETL: Mercury Emissions Control Technologies - Enhanced High Temperature  

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

Enhanced High Temperature Mercury Oxidation and Enhanced High Temperature Mercury Oxidation and In-Situ Active Carbon Generation for Low Cost Mercury Capture Mercury oxidation phenomenon and the studies of this phenomenon have generally focused on lower temperatures, typically below 650°F. This has been based on the mercury vapor equilibrium speciation curve. The baseline extents of mercury oxidation as reported in the ICR dataset and observed during subsequent tests has shown a tremendous amount of scatter. The objective of this project is to examine, establish and demonstrate the effect of higher temperature kinetics on mercury oxidation rates. Further, it is the objective of this project to demonstrate how the inherent mercury oxidation kinetics can be influenced to dramatically increase the mercury oxidation.

295

ZZ Mercury Storage Book.indb  

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

2 2 Comment Response Document Environmental Impact Statement Final Final Environmental Impact Statement DOE/EIS-0423 January 2011 Long-Term Management and Storage of Elemental Mercury Long-Term Management and Storage of Elemental Mercury For additional information on this Final Mercury Storage EIS, contact: AVAILABILITY OF THIS FINAL LONG-TERM MANAGEMENT AND STORAGE OF ELEMENTAL MERCURY ENVIRONMENTAL IMPACT STATEMENT David Levenstein, Document Manager Office of Environmental Compliance (EM-41) U.S. Department of Energy Post Office Box 2612 Germantown, MD 20874 Website: http://www.mercurystorageeis.com Fax: 877-274-5462 Printed with soy ink on recycled paper Cover Sheet Lead Agency: U.S. Department of Energy (DOE) Cooperating Agencies: U.S. Environmental Protection Agency (EPA)

296

Why 25?? and Y-12 mercury losses  

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

"25"? and Y-12 mercury losses Recently I learned something new regarding the "shortcut names" or code names for uranium-235 and plutonium-239. It seems the codes used to discuss...

297

Filter for isotopic alteration of mercury vapor  

DOE Green Energy (OSTI)

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

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

1989-01-01T23:59:59.000Z

298

Filter for isotopic alteration of mercury vapor  

DOE Patents (OSTI)

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

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

1989-06-13T23:59:59.000Z

299

Mercury sorbent delivery system for flue gas  

DOE Patents (OSTI)

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

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

2009-02-24T23:59:59.000Z

300

Analysis of Alternative Mercury Control Strategies  

Reports and Publications (EIA)

This analysis responds to a September 14, 2004, request from Chairmen James M. Inhofe and George V. Voinovich asking the Energy Information Administration (EIA) to analyze the impacts of different approaches for removing mercury from coal-fired power plants.

Alan Beamon

2005-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

NETL: Mercury Emissions Control Technologies - Utilization of...  

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

for mercury removal is produced from coal in a gasification process in-situ at coal burning plant. The main objective of this project is to obtained technical information...

302

Remediation of Mercury and Industrial Contaminants  

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

The mission of the Remediation of Mercury and Industrial Contaminants Applied Field Research Initiative is to control the flux of contaminants in soil and water environments for the purpose of...

303

NETL: News Release - Meeting Mercury Standards  

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

June 18, 2001 June 18, 2001 Meeting Mercury Standards DOE Selects 6 Projects to Develop Cost-Saving Technologies for Curbing Mercury Emissions from Coal Power Plants Power Plant with Fish - MORGANTOWN, WV - With President Bush's National Energy Plan calling for mandatory reductions in the release of mercury from electric power plants - part of the Plan's multi-pollutant reduction strategy - the U.S. Department of Energy today named six new projects to develop innovative technologies that can curb mercury emissions from coal plants more effectively and at a fraction of today's costs. The winning projects were submitted by the University of North Dakota's Energy & Environmental Research Center in Grand Forks; URS Group. Inc., of Austin, TX; CONSOL, Inc., of Library, PA; Southern Research Institute in

304

Symplectic Integrator Mercury: Bug Report  

E-Print Network (OSTI)

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

K. de Souza Torres; D. R. Anderson

2008-08-04T23:59:59.000Z

305

Why mercury prefers soft ligands  

Science Conference Proceedings (OSTI)

Mercury (Hg) is a major global pollutant arising from both natural and anthropogenic sources. Defining the factors that determine the relative affinities of different ligands for the mercuric ion, Hg2+, is critical to understanding its speciation, transformation, and bioaccumulation in the environment. Here, we use quantum chemistry to dissect the relative binding free energies for a series of inorganic anion complexes of Hg2+. Comparison of Hg2+ ligand interactions in the gaseous and aqueous phases shows that differences in interactions with a few, local water molecules led to a clear periodic trend within the chalcogenide and halide groups and resulted in the well-known experimentally observed preference of Hg2+ for soft ligands such as thiols. Our approach establishes a basis for understanding Hg speciation in the biosphere.

Riccardi, Demian M [ORNL] [ORNL; Guo, Hao-Bo [ORNL] [ORNL; Gu, Baohua [ORNL] [ORNL; Parks, Jerry M [ORNL] [ORNL; Summers, Anne [University of Georgia, Athens, GA] [University of Georgia, Athens, GA; Miller, S [University of California, San Francisco] [University of California, San Francisco; Liang, Liyuan [ORNL] [ORNL; Smith, Jeremy C [ORNL] [ORNL

2013-01-01T23:59:59.000Z

306

SCR Catalyst Management for Mercury Control  

Science Conference Proceedings (OSTI)

A number of EPRI projects conducted over the past several years have examined the effects of SCR catalyst on mercury speciation. These projects have focused on the various factors influencing mercury oxidation, related to both the flue gas conditions and the catalysts themselves. However, the majority of these studies have only examined the speciation at the SCR inlet and outlet. Much less is known about the interlayer speciation, however, which is very important when developing catalyst management ...

2012-11-16T23:59:59.000Z

307

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

308

Systematic Engineering of Phytochelatin Synthesis and Arsenic Transport for Enhanced Arsenic  

E-Print Network (OSTI)

to achieve an arsenic accumulation level of 16.8 mmol/g DCW, a 80-fold improvement when compared to a controlMT) and an As transporter GlpF. The whole cell As level of 8.1 mmol/g dry cell weight (DCW) is three times higher than other/g DCW is 20% higher than our previous reported value of 8.1 mmol/ g DCW using cells expressing Glp

Chen, Wilfred

309

Biological treatment of concentrated hazardous, toxic, and radionuclide mixed wastes without dilution  

E-Print Network (OSTI)

Hazardous, Toxic, and Radionuclide Mixed Wastes Without1997). Less volatile radionuclides are collected with 3 ofmeet the permissible radionuclide concentration and were not

Stringfellow, William T.; Komada, Tatsuyuki; Chang, Li-Yang

2004-01-01T23:59:59.000Z

310

Modeling studies of mountain-scale radionuclide transport in the unsaturated zone at Yucca Mountain, Nevada  

E-Print Network (OSTI)

Wu, and G.S. Bodvarsson, Radionuclide Transport Models Underdaughters of certain radionuclides. Increasing infiltrationOF MOUNTAIN-SCALE RADIONUCLIDE TRANSPORT IN THE UNSATURATED

Moridis, George J.; Seol, Yongkoo; Wu, Yu-Shu

2003-01-01T23:59:59.000Z

311

EFFECT OF SOURCE BOUNDARY CONDITIONS IN PREDICTING THE MIGRATION OF RADIONUCLIDES THROUGH GEOLOGIC MEDIA  

E-Print Network (OSTI)

concentra tions of radionuclides undergoing hydrogeologicRelease of Decaying Radionuclides Through Sorbing Media,"of the Tnms- port of a Radionuclide Chain Through a Sorbing

Harada, M.

2013-01-01T23:59:59.000Z

312

Article Removal of Mercury by Foam Fractionation Using Surfactin,  

E-Print Network (OSTI)

Abstract: The separation of mercury ions from artificially contaminated water by the foam fractionation process using a biosurfactant (surfactin) and chemical surfactants (SDS and Tween-80) was investigated in this study. Parameters such as surfactant and mercury concentration, pH, foam volume, and digestion time were varied and their effects on the efficiency of mercury removal were investigated. The recovery efficiency of mercury ionsInt. J. Mol. Sci. 2011, 12 8246 was highly sensitive to the concentration of the surfactant. The highest mercury ion recovery by surfactin was obtained using a surfactin concentration of 10 CMC, while recovery using SDS required 10 CMC. However, the enrichment of mercury

A Biosurfactant; Hau-ren Chen; Chien-cheng Chen; A. Satyanarayana Reddy; Chien-yen Chen; Wun Rong Li; Min-jen Tseng; Hung-tsan Liu; Wei Pan; Jyoti Prakash Maity; Shashi B. Atla

2011-01-01T23:59:59.000Z

313

Various Arsenic Treatments in Non-Ferrous Metallurgy and Other ...  

Science Conference Proceedings (OSTI)

Presentation Title, Various Arsenic Treatments in Non-Ferrous Metallurgy and ... from the Coking Wastewater Using Three-Dimensional Electrode Reactor ... Phase Equilibrium and Characterization Studies of Binary Organic Thermal Energy...

314

XAFS Study of Arsenical Nickel Hydroxide , Z. Arthur2  

E-Print Network (OSTI)

and immobilization of arsenic in uranium mine tailings. Other common co-ions in the industrial solutions formed under the similar conditions of the uranium mine tailings neutralization process. The samples

315

Treatment of arsenic-contaminated water using akaganeite adsorption  

DOE Patents (OSTI)

The present invention comprises a method and composition using akaganeite, an iron oxide, as an ion adsorption medium for the removal of arsenic from water and affixing it onto carrier media so that it can be used in filtration systems.

Cadena C., Fernando (Las Cruces, NM); Johnson, Michael D. (Las Cruces, NM)

2008-01-01T23:59:59.000Z

316

Preparation of Radiopharmaceuticals Labeled with Metal Radionuclides  

Science Conference Proceedings (OSTI)

The overall goal of this project was to develop methods for the production of metal-based radionuclides, to develop metal-based radiopharmaceuticals and in a limited number of cases, to translate these agents to the clinical situation. Initial work concentrated on the application of the radionuclides of Cu, Cu-60, Cu-61 and Cu-64, as well as application of Ga-68 radiopharmaceuticals. Initially Cu-64 was produced at the Missouri University Research Reactor and experiments carried out at Washington University. A limited number of studies were carried out utilizing Cu-62, a generator produced radionuclide produced by Mallinckrodt Inc. (now Covidien). In these studies, copper-62-labeled pyruvaldehyde Bis(N{sup 4}-methylthiosemicarbazonato)-copper(II) was studied as an agent for cerebral myocardial perfusion. A remote system for the production of this radiopharmaceutical was developed and a limited number of patient studies carried out with this agent. Various other copper radiopharmaceuticals were investigated, these included copper labeled blood imaging agents as well as Cu-64 labeled antibodies. Cu-64 labeled antibodies targeting colon cancer were translated to the human situation. Cu-64 was also used to label peptides (Cu-64 octriatide) and this is one of the first applications of a peptide radiolabeled with a positron emitting metal radionuclide. Investigations were then pursued on the preparation of the copper radionuclides on a small biomedical cyclotron. A system for the production of high specific activity Cu-64 was developed and initially the Cu-64 was utilized to study the hypoxic imaging agent Cu-64 ATSM. Utilizing the same target system, other positron emitting metal radionuclides were produced, these were Y-86 and Ga-66. Radiopharmaceuticals were labeled utilizing both of these radionuclides. Many studies were carried out in animal models on the uptake of Cu-ATSM in hypoxic tissue. The hypothesis is that Cu-ATSM retention in vivo is dependent upon the oxygen retention of the tissue and the significantly greater retention amounting in hypoxic tissue. This hypothesis was confirmed in a series of animal studies. Cu-64 can be used both as an imaging radionuclide and a therapeutic radionuclide. The therapeutic efficacy of Cu-64 ATSM was proven in hamsters bearing the CW39 human colorectal tumors. The administration of Cu-64 ATSM significantly increased the survival time of tumor-bearing animals with no acute toxicity. This copper agent therefore shows promise for radiotherapy. The flow tracer Cu-64 PTSM also demonstrates therapeutic potential by inhibiting cancer cells implanted in animal models. Again, this inhibition occurred at doses which showed no sign of toxicity to the animals. Cu-ATSM was translated to humans, under other support a series of tumors were investigated; these included head and neck cancer, non-small cell lung cancer, cervical cancer and renal cancer. Another radionuclide that was investigated was titanium 45. This radionuclide was successfully produced by radiation of a scandium foil with 15 MeV protons. The titanium 45 was processed and separated from residual scandium by high exchange chomotrophy. Titanium titanocene has been utilized as a therapeutic agent; this compound was prepared and studied in vitro and in vivo. Another project was the preparation of cyclodextrin dimers as a new pre-targeting approach for tumor uptake. Beta-cyclodextradin and two other dimers were synthesized. These dimers were studied for the in vivo application. Work continued on the application of the radionuclide already discussed. Technetium 94m, a positron emitting radionuclide of the widely used 99m Tc nuclide was also prepared. This allows the quantification of the uptake of technetium radiopharmaceuticals. In collaboration with Professor David Piwnica-Worms, technetium 94m, sestamibi was studied in animal models and in a limited number of human subjects.

Welch, M.J.

2012-02-16T23:59:59.000Z

317

Idaho radionuclide exposure study: Literature review  

Science Conference Proceedings (OSTI)

Phosphate ores contain elevated levels of natural radioactivity, some of which is released to the environment during processing or use of solid byproducts. The effect of radionuclides from Idaho phosphate processing operations on the local communities has been the subject of much research and study. The literature is reviewed in this report. Two primary radionuclide pathways to the environment have been studied in detail: (1) airborne release of volatile radionuclides, primarily /sup 210/Po, from calciner stacks at the two elemental phosphorus plants; and (2) use of byproduct slag as an aggregate for construction in Soda Springs and Pocatello. Despite the research, there is still no clear understanding of the population dose from radionuclide emissions, effluents, and solid wastes from phosphate processing plants. Two other potential radionuclide pathways to the environment have been identified: radon exhalation from phosphogypsum and ore piles and contamination of surface and ground waters. Recommendations on further study needed to develop a data base for a complete risk assssment are given in the report.

Baker, E.G.; Freeman, H.D.; Hartley, J.N.

1987-10-01T23:59:59.000Z

318

Radionuclide Air Emission Report for 2011  

SciTech Connect

Berkeley Lab operates facilities where radionuclides are produced, handled, stored, and potentially emitted. These facilities are subject to the EPA radioactive air emission regulations in 40 CFR 61, Subpart H. Radionuclides may be emitted from stacks or vents on buildings where radionuclide production or use is authorized or they may be emitted as diffuse sources. In 2011, all Berkeley Lab sources were minor sources of radionuclides (sources resulting in a potential dose of less than 0.1 mrem/yr [0.01 mSv/yr]). These minor sources included about 90 stack sources and one source of diffuse emissions. There were no unplanned airborne radionuclide emissions from Berkeley lab operations. Emissions from minor sources (stacks and diffuse emissions) were measured by sampling or monitoring or were calculated based on quantities used, received for use, or produced during the year. Using measured and calculated emissions, and building-specific and common parameters, Laboratory personnel applied the EPA-approved computer codes, CAP88-PC and COMPLY, to calculate the effective dose equivalent to the maximally exposed individual (MEI).

Wahl, Linnea

2012-06-04T23:59:59.000Z

319

Radionuclide Retention in Concrete Waste Forms  

Science Conference Proceedings (OSTI)

Assessing long-term performance of Category 3 waste cement grouts for radionuclide encasement requires knowledge of the radionuclide-cement interactions and mechanisms of retention (i.e., sorption or precipitation); the mechanism of contaminant release; the significance of contaminant release pathways; how waste form performance is affected by the full range of environmental conditions within the disposal facility; the process of waste form aging under conditions that are representative of processes occurring in response to changing environmental conditions within the disposal facility; the effect of waste form aging on chemical, physical, and radiological properties; and the associated impact on contaminant release. This knowledge will enable accurate prediction of radionuclide fate when the waste forms come in contact with groundwater. The information presented in the report provides data that 1) quantify radionuclide retention within concrete waste form materials similar to those used to encapsulate waste in the Low-Level Waste Burial Grounds (LLBG); 2) measure the effect of concrete waste form properties likely to influence radionuclide migration; and 3) quantify the stability of uranium-bearing solid phases of limited solubility in concrete.

Mattigod, Shas V.; Bovaird, Chase C.; Wellman, Dawn M.; Wood, Marcus I.

2010-09-30T23:59:59.000Z

320

Radionuclide Retention in Concrete Wasteforms - FY13  

SciTech Connect

Assessing long-term performance of Category 3 waste cement grouts for radionuclide encasement requires knowledge of the radionuclide-cement interactions and mechanisms of retention (i.e., sorption or precipitation); the mechanism of contaminant release; the significance of contaminant release pathways; how wasteform performance is affected by the full range of environmental conditions within the disposal facility; the process of wasteform aging under conditions that are representative of processes occurring in response to changing environmental conditions within the disposal facility; the effect of wasteform aging on chemical, physical, and radiological properties; and the associated impact on contaminant release. This knowledge will enable accurate prediction of radionuclide fate when the wasteforms come in contact with groundwater. Data collected throughout the course of this work will be used to quantify the efficacy of concrete wasteforms, similar to those used in the disposal of low-level waste and mixed low-level waste, for the immobilization of key radionuclides (i.e., uranium, technetium, and iodine). Data collected will also be used to quantify the physical and chemical properties of the concrete affecting radionuclide retention.

Snyder, Michelle MV; Golovich, Elizabeth C.; Wellman, Dawn M.; Crum, Jarrod V.; Lapierre, Robert; Dage, Denomy C.; Parker, Kent E.; Cordova, Elsa A.

2013-10-15T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Arsenic and Selenium Treatment Technology Summary for Power Plant Wastewaters  

Science Conference Proceedings (OSTI)

This report summarizes the most suitable technologies available for the removal of arsenic and selenium from power plant wastewaters. The information stems from literature searches and the authors' experience in wastewater treatment systems from generally non-power plant sources since there are limited operating experiences for power plant applications. The report lists existing and potential technologies that meet the treatment goals of reducing arsenic and selenium to the levels set for U.S. En...

2004-11-03T23:59:59.000Z

322

Residential exposure to drinking water arsenic in Inner Mongolia, China  

SciTech Connect

In the Ba Men region of Inner Mongolia, China, a high prevalence of chronic arsenism has been reported in earlier studies. A survey of the arsenic contamination among wells from groundwater was conducted to better understand the occurrence of arsenic (As) in drinking water. A total of 14,866 wells (30% of all wells in the region) were analyzed for their arsenic-content. Methods used to detect arsenic were Spectrophotometric methods with DCC-Ag (detection limit, 0.5 {mu}g of As/L); Spot method (detection limit, 10 {mu}g of As/L); and air assisted Colorimetry method (detection limit, 20 {mu}g of As/L). Arsenic-concentrations ranged from below limit of detection to 1200 {mu}g of As/L. Elevated concentrations were related to well depth (10 to 29 m), the date the well was built (peaks from 1980-1990), and geographic location (near mountain range). Over 25,900 individuals utilized wells with drinking water arsenic concentrations above 20 {mu}g of As/L (14,500 above 50 {mu}g of As/L-the current China national standard in drinking water and 2198 above 300 {mu}g of As/L). The presented database of arsenic in wells of the Ba Men region provides a useful tool for planning future water explorations when combined with geological information as well as support for designing upcoming epidemiological studies on the effects of arsenic in drinking water for this region.

Ning Zhixiong [Ba Men Anti-Epidemic Station, Lin He, Inner Mongolia (China); Lobdell, Danelle T. [Epidemiology and Biomarkers Branch, Human Studies Division, National Health and Environmental Effects Research Laboratory, U.S. EPA, Chapel Hill (United States); Kwok, Richard K. [RTI International, P.O. Box 12194, 3040 Cornwallis Rd, Research Triangle Park, NC 27709-2194 (United States)], E-mail: rkwok@rti.org; Liu Zhiyi; Zhang Shiying; Ma Chenglong [Ba Men Anti-Epidemic Station, Lin He, Inner Mongolia (China); Riediker, Michael [Institut Universitaire Romand de Sante au Travail, Lausanne (Switzerland); Mumford, Judy L. [Epidemiology and Biomarkers Branch, Human Studies Division, National Health and Environmental Effects Research Laboratory, U.S. EPA, Chapel Hill (United States)

2007-08-01T23:59:59.000Z

323

Identification of Arsenic Species in Coal Ash Particles  

Science Conference Proceedings (OSTI)

Identification of the chemical species and compounds of arsenic in individual coal fly ash particles will help provide a scientifically sound basis for assessing health risks from inhalation of these particles. This report presents the results of an analytical chemistry study of coal-combustion ash, with some work also completed on oil-combustion ash and copper smelter dust collected from several sources in the United States and Europe. Results showed that most arsenic is present on the surface of coal a...

1998-08-13T23:59:59.000Z

324

Characterization of Arsenic Contamination on Rust from Ton Containers  

Science Conference Proceedings (OSTI)

The speciation and spatial distribution of arsenic on rusted steel surfaces affects both measurement and removal approaches. The chemistry of arsenic residing in the rust of ton containers that held the chemical warfare agents bis(2-chloroethyl)sulfide (sulfur mustard) and 2-chlorovinyldichloroarsine (Lewisite) is of particular interest, because while the agents have been decontaminated, residual arsenic could pose a health or environmental risk. The chemistry and distribution of arsenic in rust samples was probed using imaging secondary ion mass spectrometry (SIMS), X-ray photoelectron spectroscopy (XPS), Auger electron spectroscopy, and scanning electron microscopy/energy dispersive X-ray spectroscopy (SEM/EDX). Arsenic in the +3 and or +5 oxidation state is homogeneously distributed at the very top-most layer of the rust samples, and is intimately associated with iron. Sputter depth profiling followed by SIMS and XPS shows As at a depth of several nm, in some cases in a reduced form. The SEM/EDX experiments show that As is present at a depth of several microns, but is inhomogeneously distributed; most locations contained oxidized As at concentrations of a few percent, however several locations showed very high As in a metallic form. These results indicate that the rust material must be removed if the steel containers are to be cleared of arsenic.

Gary S. Groenewold; Recep Avci; Robert V. Fox; Muhammedin Deliorman; Jayson Suo; Laura Kellerman

2013-01-01T23:59:59.000Z

325

Diffusion of Radionuclides in Concrete and Soil  

SciTech Connect

One of the methods being considered for safely disposing of Category 3 low-level radioactive wastes is to encase the waste in concrete. Such concrete encasement would contain and isolate the waste packages from the hydrologic environment and would act as an intrusion barrier. Any failure of concrete encasement may result in water intrusion and consequent mobilization of radionuclides from the waste packages. The mobilized radionuclides may escape from the encased concrete by mass flow and/or diffusion and move into the surrounding subsurface environment. Therefore, it is necessary to assess the performance of the concrete encasement structure and the ability of the surrounding soil to retard radionuclide migration. The objective of our study was to measure the diffusivity of Re, Tc and I in concrete containment and the surrounding vadose zone soil. Effects of carbonation, presence of metallic iron, and fracturing of concrete and the varying moisture contents in soil on the diffusivities of Tc and I were evaluated.

Mattigod, Shas V.; Wellman, Dawn M.; Bovaird, Chase C.; Parker, Kent E.; Recknagle, Kurtis P.; Clayton, Libby N.; Wood, Marcus I.

2012-04-25T23:59:59.000Z

326

On the oscillations in Mercury's obliquity  

E-Print Network (OSTI)

One major objective of MESSENGER and BepiColombo spatial missions is to accurately measure Mercury's rotation and its obliquity in order to obtain constraints on internal structure of the planet. Which is the obliquity's dynamical behavior deriving from a complete spin-orbit motion of Mercury simultaneously integrated with planetary interactions? We have used our SONYR model integrating the spin-orbit N-body problem applied to the solar System (Sun and planets). For lack of current accurate observations or ephemerides of Mercury's rotation, and therefore for lack of valid initial conditions for a numerical integration, we have built an original method for finding the libration center of the spin-orbit system and, as a consequence, for avoiding arbitrary amplitudes in librations of the spin-orbit motion as well as in Mercury's obliquity. The method has been carried out in two cases: (1) the spin-orbit motion of Mercury in the 2-body problem case (Sun-Mercury) where an uniform precession of the Keplerian orbital plane is kinematically added at a fixed inclination (S2K case), (2) the spin-orbit motion of Mercury in the N-body problem case (Sun and planets) (Sn case). We find that the remaining amplitude of the oscillations in the Sn case is one order of magnitude larger than in the S2K case, namely 4 versus 0.4 arcseconds (peak-to-peak). The mean obliquity is also larger, namely 1.98 versus 1.80 arcminutes, for a difference of 10.8 arcseconds. These theoretical results are in a good agreement with recent radar observations but it is not excluded that it should be possible to push farther the convergence process by drawing nearer still more precisely to the libration center.

E. Bois; N. Rambaux

2007-09-07T23:59:59.000Z

327

Evaluation of Sorbent Injection for Mercury Control  

Science Conference Proceedings (OSTI)

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

Sharon Sjostrom

2005-12-30T23:59:59.000Z

328

DOE Issues Final Mercury Storage Environmental Impact Statement: Texas Site  

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

DOE Issues Final Mercury Storage Environmental Impact Statement: DOE Issues Final Mercury Storage Environmental Impact Statement: Texas Site Is Preferred for Long-Term Mercury Storage DOE Issues Final Mercury Storage Environmental Impact Statement: Texas Site Is Preferred for Long-Term Mercury Storage January 19, 2011 - 12:00pm Addthis Media Contact (202) 586-4940 WASHINGTON - The Department of Energy has prepared a Final Long-Term Management and Storage of Elemental Mercury Environmental Impact Statement to analyze the potential environmental, human health, and socioeconomic impacts of elemental mercury storage at seven locations. Based on these factors, DOE identified the Waste Control Specialists, LLC, site near Andrews, Texas, as the preferred alternative for long-term management and storage of mercury. DOE will consider the environmental impact information presented in this

329

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

Open Energy Info (EERE)

Mercury Vapor At Kawaihae Area (Thomas, 1986) Mercury Vapor At Kawaihae Area (Thomas, 1986) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Kawaihae Area (Thomas, 1986) Exploration Activity Details Location Kawaihae Area Exploration Technique Mercury Vapor Activity Date Usefulness not useful DOE-funding Unknown Notes The soil geochemistry yielded quite complex patterns of mercury concentrations and radonemanation rates within the survey area (Cox and Cuff, 1981c). Mercury concentrations (Fig. 38) showed a general minimum along the Kawaihae-Waimea roads and a broad trend of increasing mercury concentrations toward both the north and south. There is no correlation apparent between the mercury patterns and either the resistivity sounding data or the surface geology in the area. The radon emanometry data (Fig.

330

Laser altimeter measurements from MESSENGER's recent mercury flybys  

E-Print Network (OSTI)

The performance of the Mercury Laser Altimeter is reported from MESSENGER's flybys of Mercury in January and October 2008. The instrument ranged to 600 km at >60deg incidence angle and 1600 km in nadir direction.

Sun, Xiaoli

331

Seismic effects of the Caloris basin impact, Mercury  

E-Print Network (OSTI)

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

L, Jiangning

2011-01-01T23:59:59.000Z

332

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

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

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

333

Mercurial commitments with applications to zero-knowledge sets  

Science Conference Proceedings (OSTI)

We introduce a new flavor of commitment schemes, which we call mercurial commitments. Informally, mercurial commitments are standard commitments that have been extended to allow for soft decommitment. Soft decommitments, on the one hand, ...

Melissa Chase; Alexander Healy; Anna Lysyanskaya; Tal Malkin; Leonid Reyzin

2005-05-01T23:59:59.000Z

334

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

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

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

335

Removal of mercury from coal via a microbial pretreatment process  

Science Conference Proceedings (OSTI)

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

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

2011-08-16T23:59:59.000Z

336

Laboratory studies of radionuclide migration in tuff  

SciTech Connect

The movement of selected radionuclides has been observed in crushed tuff, intact tuff, and fractured tuff columns. Retardation factors and dispersivities were determined from the elution profiles. Retardation factors have been compared with those predicted on the basis of batch sorption studies. This comparison forms a basis for either validating distribution coefficients or providing evidence of speciation, including colloid formation. Dispersivities measured as a function of velocity provide a means of determining the effect of sorption kinetics or mass transfer on radionuclide migration. Dispersion is also being studied in the context of scaling symmetry to develop a basis for extrapolating from the laboratory scale to the field. 21 refs., 6 figs., 2 tabs.

Rundberg, R.S.; Mitchell, A.J.; Ott, M.A.; Thompson, J.L.; Triay, I.R.

1989-10-01T23:59:59.000Z

337

NIST: Mercury, Atomic Ref. Data for Elect. Struct. Calc.  

Science Conference Proceedings (OSTI)

Table of contents logo, Atomic Reference Data for Electronic Structure Calculations. Mercury. Key to notation | HTML table ...

338

Mercury in Nelsons Sparrow Subspecies at Breeding Sites  

E-Print Network (OSTI)

Background: Mercury is a persistent, biomagnifying contaminant that can cause negative effects on ecosystems. Marshes are often areas of relatively high mercury methylation and bioaccumulation. Nelsons Sparrows (Ammodramus nelsoni) use marsh habitats year-round and have been documented to exhibit tissue mercury concentrations that exceed negative effects thresholds. We sought to further characterize the potential risk of Nelsons Sparrows to mercury exposure by sampling individuals from sites within the range of each of its subspecies.

Virginia L Winder; Steven D. Emslie

2012-01-01T23:59:59.000Z

339

U.S. Mercury Deposition Under Alternative Regulatory Scenarios  

Science Conference Proceedings (OSTI)

The Federal Clean Air Mercury Rule regulates electric utility mercury emissions while permitting individual states to enact stricter rules at their discretion. Computer modeling has shown how mercury deposition patterns will change if all regulated utility power plants follow the Federal rule, vs. alternative state rules. These patterns of deposition can be compared to the limiting case: what if all U.S. utility mercury emissions were zeroed out? The findings show that regulations stricter than the Feder...

2007-12-14T23:59:59.000Z

340

Selective Catalytic Reduction Mercury Oxidation Data to Support Catalyst Management  

Science Conference Proceedings (OSTI)

Selective catalytic reduction (SCR) mercury oxidation can be pivotal for Mercury and Air Toxics Standards compliance, especially for those units that rely on co-benefits as their primary method of mercury control. Much work has been done historically to understand the mercury behavior across SCRs, especially as a function of operating conditions, and in particular, flue gas composition. The present work seeks to integrate the accumulated knowledge into a practical document that will aid utilities in ...

2013-11-13T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

End of an Era: NIST to Cease Calibrating Mercury ...  

Science Conference Proceedings (OSTI)

... Burning of coal is a major source of vaporous mercury released into the atmosphere. Compact fluorescents use less electricity ...

2011-10-03T23:59:59.000Z

342

Bench-scale studies with mercury contaminated SRS soil  

SciTech Connect

Bench-scale studies with mercury contaminated soil were performed at the SRTC to determine the optimum waste loading obtainable in the glass product without sacrificing durability, leach resistance, and processability. Vitrifying this waste stream also required offgas treatment for the capture of the vaporized mercury. Four soil glasses with slight variations in composition were produced, which were capable of passing the Product Consistency Test (PCT) and the Toxicity Characteristic Leaching Procedure (TCLP). The optimum glass feed composition contained 60 weight percent soil and produced a soda-lime-silica glass when melted at 1,350 C. The glass additives used to produce this glass were 24 weight percent Na{sub 2}CO{sub 3} and 16 weight percent CaCO{sub 3}. Volatilized mercury released during the vitrification process was released to the proposed mercury collection system. The proposed mercury collection system consisted of quartz and silica tubing with a Na{sub 2}S wash bottle followed by a NaOH wash bottle. Once in the system, the volatile mercury would pass through the wash bottle containing Na{sub 2}S, where it would be converted to Hg{sub 2}S, which is a stable form of mercury. However, attempts to capture the volatilized mercury in a Na{sub 2}S solution wash bottle were not as successful as anticipated. Maximum mercury captured was only about 3.24% of the mercury contained in the feed. Mercury capture efforts then shifted to condensing and capturing the volatilized mercury. These attempts were much more successful at capturing the volatile mercury, with a capture efficiency of 34.24% when dry ice was used to pack the condenser. This captured mercury was treated on a mercury specific resin after digestion of the volatilized mercury.

Cicero, C.A.

1995-12-31T23:59:59.000Z

343

Fission modes of mercury isotopes  

E-Print Network (OSTI)

Background: Recent experiments on beta-delayed fission in the mercury-lead region and the discovery of asym- metric fission in 180 Hg [1] have stimulated theoretical interest in the mechanism of fission in heavy nuclei. Purpose: We study fission modes and fusion valleys in 180 Hg and 198 Hg to reveal the role of shell effects in pre-scission region and explain the experimentally observed fragment mass asymmetry and its variation with A. Methods: We use the self-consistent nuclear density functional theory employing Skyrme and Gogny energy density functionals. Results: The potential energy surfaces in multi-dimensional space of collective coordinates, including elongation, triaxiality, reflection-asymmetry, and necking, are calculated for 180 Hg and 198 Hg. The asymmetric fission valleys - well separated from fusion valleys associated with nearly spherical fragments - are found in in both cases. The density distributions at scission configurations are studied and related to the experimentally observed mass splits. Conclusions: The energy density functionals SkM\\ast and D1S give a very consistent description of the fission process in 180 Hg and 198 Hg. We predict a transition from asymmetric fission in 180 Hg towards more symmetric distribution of fission fragments in 198 Hg. For 180 Hg, both models yield 100 Ru/80 Kr as the most probable split. For 198 Hg, the most likely split is 108 Ru/90 Kr in HFB-D1S and 110 Ru/88 Kr in HFB-SkM\\ast.

M. Warda; A. Staszczak; W. Nazarewicz

2012-05-25T23:59:59.000Z

344

Fission Modes of Mercury Isotopes  

Science Conference Proceedings (OSTI)

Background: Recent experiments on -delayed fission in the mercury-lead region and the discovery of asymmetric fission in 180Hg [A. N. Andreyev et al., Phys. Rev. Lett. 105, 252502 (2010)] have stimulated theoretical interest in the mechanism of fission in heavy nuclei. Purpose: We study fission modes and fusion valleys in 180Hg and 198Hg to reveal the role of shell effects in the prescission region and explain the experimentally observed fragment mass asymmetry and its variation with A. Methods: We use the self-consistent nuclear density functional theory employing Skyrme and Gogny energy density functionals. Results: The potential energy surfaces in multidimensional space of collective coordinates, including elongation, triaxiality, reflection-asymmetry, and necking, are calculated for 180Hg and 198Hg. The asymmetric fission valleys well separated from fusion valleys associated with nearly spherical fragments are found in both cases. The density distributions at scission configurations are studied and related to the experimentally observed mass splits. Conclusions: The energy density functionals SkM and D1S give a very consistent description of the fission process in 180Hg and 198Hg. We predict a transition from asymmetric fission in 180Hg toward a more symmetric distribution of fission fragments in 198Hg. For 180Hg, both models yield 100Ru/80Kr as the most probable split. For 198Hg, the most likely split is 108Ru/90Kr in HFB-D1S and 110Ru/88Kr in HFB-SkM .

Warda, M. [Maria Curie-Sk?odowska University-Poland; Staszczak, A. [Maria Curie-Sklodowska University; Nazarewicz, Witold [UTK/ORNL/University of Warsaw

2012-01-01T23:59:59.000Z

345

Mercury-free fluorescent lighting  

Science Conference Proceedings (OSTI)

A brief comparative review of possible mercury free fluorescent lighting technologies is presented, including rare-gas positive column discharges, molecular discharges, and dielectric barrier discharges. Detailed experimental results on xenon positive column discharges will then be considered. In order to judge whether xenon-based discharges are a viable UV source it is necessary to measure the radiant emittance (power per unit area) for the vacuum ultraviolet (VUV) resonance xenon emission at 147 nm. Two techniques to determine the VUV radiant emittance have been developed and applied to xenon discharges. One method combines the measured resonance level density using absorption spectroscopy and a calculation of the trapped decay rate for the resonance radiation to arrive at the radiant emittance at 147 nm. A second method utilizes a direct measurement of the radiance (power per unit area per unit solid angle) at 147 nm using a calibrated VUV photodiode, and a calculation of the relative angular distribution of the resonance radiation to determine the radiant emittance. In both techniques a simulation of the transport of resonance radiation is key to determining the radiant emittance.

Doughty, D.A. [General Electric Corporate Research and Development, Schenectady, NY (United States)

1996-05-01T23:59:59.000Z

346

Mercury Removal Characteristics of Coal-Fired Power Plants  

Science Conference Proceedings (OSTI)

The standard Ontario Hydro Method (OHM) was used into the flue gas mercury sampling before and after fabric filter (FF)/ electrostatic precipitator (ESP) locations in coal-fired power stations in China, and then various mercury speciation, Hg0, Hg2+ ... Keywords: coal-fired power plant, mercury, fabric filter, electrostatic precipitator

Yang Liguo, Fan Xiaoxu, Duanyu Feng, Wang Yunjun

2013-01-01T23:59:59.000Z

347

MERCURY HANDLING FOR THE TARGET SYSTEM FOR A MUON COLLIDER  

E-Print Network (OSTI)

Cryostat 1. Remote handling The high radiation levels and presence of hazardous, ac- tivated mercury vaporsMERCURY HANDLING FOR THE TARGET SYSTEM FOR A MUON COLLIDER Van Graves , ORNL, Oak Ridge, TN 37830 placement within the Shielding Module in a remote environment. · Providing double containment of the mercury

McDonald, Kirk

348

MERCURY CONTROL FOR MWCs USING THE SODIUM TETRASULFIDE PROCESS  

E-Print Network (OSTI)

technologies for mercury control for flue gases of Municipal Waste Combustors (MWCs) not only ecological hydrochloric acid (HCl) and elemental mercury (Hg") under oxidizing conditions of the off-gases downstream to the decreasing gas temperature, the elemental mercury is able to react with other flue gas components. The main

Columbia University

349

PEER-REVIEW An Experimental Study on Mercury Sorption by  

E-Print Network (OSTI)

flue gases. These studies have shown the relative ease of controlling oxidized mercury (specifically, Nashville, 1996 8. B. Hall, O . Lindqvist, and E. Ljungstrom, "Mercury Chemistry in Simulated Flue Gases municipal waste combustor (MWC), flue gas mercury is mainly found as HgCI2. They postulated thatHgCl2

Columbia University

350

Mercury and Dioxin Control for Municipal Waste Combustors Anthony Licata  

E-Print Network (OSTI)

) and elemental mercury (Hg«» under oxidizing conditions of the off-gases downstream of the refuse incinerator), sulfur dioxide (S02)' nitrogen oxides (NOx), carbon monoxide (CO), PCDDs/PCDFs, cadmium (Cd), mercury (Hg emission regulations. Mercury Control in MWCs The capture of Hg in flue gas cleaning devices depends on the

Columbia University

351

National Waste Processing Conference Proceedings ASME 1994 ACID GASES, MERCURY,  

E-Print Network (OSTI)

) and elemental mercury (Hg«» under oxidizing conditions of the off-gases downstream of the refuse incinerator), sulfur dioxide (S02)' nitrogen oxides (NOx), carbon monoxide (CO), PCDDs/PCDFs, cadmium (Cd), mercury (Hg emission regulations. Mercury Control in MWCs The capture of Hg in flue gas cleaning devices depends on the

Columbia University

352

Radionuclide Behavior and Geochemistry in Boom Clay after ...  

Science Conference Proceedings (OSTI)

Radioactive Demonstrations of Fluidized Bed Steam Reforming (FBSR) with Hanford Low Activity Wastes Radionuclide Behavior and Geochemistry in Boom ...

353

Biomethylation of inorganic arsenic by the rat and some laboratory animals  

SciTech Connect

This article concerns the distribution (in the liver, kidney and blood) and excretion (in the urine, feces and bile) of arsenic metabolites such as dimethylated, monomethylated and inorganic arsenic in rats following a single oral and intravenous (iv) administration of arsenic acid. This paper also describes studies on the species difference in the arsenic methylation between the rats and some other laboratory animals as mice, hamsters, rabbits and cats.

Odanaka, Y.; Matano, O.; Goto, S.

1980-03-01T23:59:59.000Z

354

Mixed Waste Focus Area Mercury Working Group: An integrated approach to mercury waste treatment and disposal  

SciTech Connect

In May 1996, the US Department of Energy (DOE) Mixed Waste Focus Area (MWFA) initiated the Mercury Working Group (HgWG). The HgWG was established to address and resolve the issues associated with mercury contaminated mixed wastes. During the MWFA`s initial technical baseline development process, three of the top four technology deficiencies identified were related to the need for amalgamation, stabilization, and separation removal technologies for the treatment of mercury and mercury contaminated mixed waste. The HgWG is assisting the MWFA in soliciting, identifying, initiating, and managing efforts to address these areas. The focus of the HgWG is to better establish the mercury related treatment technologies at the DOE sites, refine the MWFA technical baseline as it relates to mercury treatment, and make recommendations to the MWFA on how to most effectively address these needs. Based on the scope and magnitude of the mercury mixed waste problem, as defined by HgWG, solicitations and contract awards have been made to the private sector to demonstrate both the amalgamation and stabilization processes using actual mixed wastes. Development efforts are currently being funded that will address DOE`s needs for separation removal processes. This paper discusses the technology selection process, development activities, and the accomplishments of the HgWG to date through these various activities.

Conley, T.B.; Morris, M.I.; Osborne-Lee, I.W.

1998-01-01T23:59:59.000Z

355

The mixed waste focus area mercury working group: an integrated approach for mercury treatment and disposal  

SciTech Connect

In May 1996, the U.S. Department of Energy (DOE) Mixed Waste Focus Area (MWFA) initiated the Mercury Work Group (HgWG), which was established to address and resolve the issues associated with mercury- contaminated mixed wastes. Three of the first four technology deficiencies identified during the MWFA technical baseline development process were related to mercury amalgamation, stabilization, and separation/removal. The HgWG will assist the MWFA in soliciting, identifying, initiating, and managing all the efforts required to address these deficiencies. The focus of the HgWG is to better establish the mercury-related treatment needs at the DOE sites, refine the MWFA technical baseline as it relates to mercury treatment, and make recommendations to the MWFA on how to most effectively address these needs. The team will initially focus on the sites with the most mercury-contaminated mixed wastes, whose representatives comprise the HgWG. However, the group will also work with the sites with less inventory to maximize the effectiveness of these efforts in addressing the mercury- related needs throughout the entire complex.

Conley, T.B.; Morris, M.I. [Oak Ridge National Lab., TN (United States); Holmes-Burns, H. [Westinghouse Savannah River Co., Aiken, SC (United States); Petersell, J. [AIMS, Inc., Golden, CO (United States); Schwendiman, L. [Lockheed Martin Idaho Technologies Co., Idaho Falls, ID (United States)

1997-02-01T23:59:59.000Z

356

Arsenic and antimony in laundry aids by instrumental neutron activation analysis  

SciTech Connect

>The measurement of trace amounts of arsenic and antimony in laundry aids by neutron activation analysis is described. The results for arsenic are compared with those obtained by other analytical techniques. The concentratlons ln the various laundry aids tested ranged from 5 to 51 ppM of arsenic and from 1 to 8 ppM of antimony. (auth)

Tanner, J.T.; Friedman, M.H.; Holloway, G.E.

1973-10-01T23:59:59.000Z

357

Mercury levels in Lake Powell. Bioamplification of mercury in man-made desert reservoir  

SciTech Connect

Flameless atomic absorption analyses of samples from Lake Powell yield mean mercury levels in ppb of 0.01 in water, 30 in bottom sediments, 10 in shoreline substrates, 34 in plant leaves, 145 in plant debris, 28 in algae, 10 in crayfish, and 232 in fish muscle. Trout were unique in having lower concentrations in muscle than in highly vascularized blood tissues. Concentrations increased with increased body weight and higher levels on the food chain. Muscle of some large fish over 2 kg whole body weight exceeded 500 ppb. Bioamplification of mercury up the food chain and association of mercury with organic matter are demonstrated.

Potter, L.; Kidd, D.; Standiford, D.

1975-01-01T23:59:59.000Z

358

Scientific Analysis Cover Sheet for Radionuclide Screening  

Science Conference Proceedings (OSTI)

The waste forms under consideration for disposal in the proposed repository at Yucca Mountain contain scores of radionuclides (Attachments V and VI). It would be impractical and highly inefficient to model all of these radionuclides in a total system performance assessment (TSPA). Thus, the purpose of this radionuclide screening analysis is to remove from further consideration (screen out) radionuclides that are unlikely to significantly contribute to radiation dose to the public from the proposed nuclear waste repository at Yucca Mountain. The remaining nuclides (those screened in) are recommended for consideration in TSPA modeling for license application. This analysis also covers radionuclides that are not screened in based on dose, but need to be included in TSPA modeling for other reasons. For example, U.S. Environmental Protection Agency (EPA) and U.S. Nuclear Regulatory Commission (NRC) regulations require consideration of the combined activity of Ra-226 and Ra-228 in groundwater (40 CFR 197.30, 10 CFR 63.331). Also, Cm-245, Pu-241, and U-235 decay indirectly to potentially important radionuclides, and are not identified by the screening analysis as important. The radionuclide screening analysis separately considers two different postclosure time periods: the 10,000-y regulatory period for the proposed repository at Yucca Mountain and the period after 10,000 y up to 1 million y after emplacement. The incremental effect of extending the screening for the regulatory period to 20,000 y is also addressed. Four release scenarios are considered: (1) the nominal scenario, which entails long-term degradation of disposal containers and waste forms, (2) a human-intrusion scenario, (3) an intrusive igneous event, and (4) an eruptive igneous event. Because the first three scenarios require groundwater transport, they are called groundwater scenarios below. The screening analysis considers the following waste forms: spent boiling water reactor (BWR) fuel, spent pressurized water reactor (PWR) fuel, U.S. Department of Energy (DOE) spent nuclear fuel (DSNF), and high-level waste (HLW). Average and outlying (high burnup, high initial enrichment, low age, or otherwise exceptional) forms of each waste-form type are considered. This analysis has been prepared in accordance with a technical work plan (BSC 2002c). In a review of Revision 00 of this radionuclide screening analysis, the NRC found that ''processes that affect transport in the biosphere, such as uptake by plants and bioaccumulation are not accounted for'' and that ''the direct exposure pathway is not accounted for'' (Beckman 2001, Section 5.3.2.1). The NRC also found that the solubility and sorption classes were too broadly defined, noting, for example, that Se is in the same solubility and sorptivity groups as Np and U, yet is ''more soluble than Np and U by several orders of magnitude'' (Beckman 2001, Section 5.3.2.1). This revision seeks to build upon the strengths of the earlier screening method while responding to the specific concerns raised by the NRC and other reviewers. In place of simple inhalation and ingestion dose conversion factors, the revised radionuclide screening uses screening factors that also take into account soil accumulation, uptake by plants, exposure to contaminated ground, and other features of the biosphere that were neglected in the previous screening. Whereas the previous screening analysis allowed only two solubility classes (soluble and insoluble), the revised screening introduces an intermediate solubility class to better segregate the radionuclides into transport groups.

G. Ragan

2002-08-09T23:59:59.000Z

359

NETL: Mercury Emissions Control Technologies - Advanced Utility  

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

Advanced Utility Mercury-Sorbent Field Testing Program Advanced Utility Mercury-Sorbent Field Testing Program Sorbent Technologies Corporation, will test an advanced halgenated activated carbon to determine the mercury removal performance and relative costs of sorbent injection for advanced sorbent materials in large-scale field trials of a variety of combinations of coal-type and utility plant-configuration. These include one site (Detroit Edison's St. Clair Station) with a cold-side ESP using subbituminous coal, or blend of subbituminous and bituminous coal, and one site (Duke Energy's Buck Plant) with a hot-side ESP which burns a bituminous coal. Related Papers and Publications: Semi-Annual Technical Progress Report for the period April 1 - October 31, 2004 [PDF-2275KB] Semi-Annual Technical Progress Report for the period of October 2003 - March 2004 [PDF-1108KB]

360

EVALUATION OF MERCURY COOLED BREEDER REACTORS  

SciTech Connect

A technical and economic evaluation of a mercury-cooled fast breeder reactor is presented. The objectives of the program were to establish the technical feasibility of a fast breeder reactor cooled with boiling mercury and to evaluate the long-range potential of such a reactor power plant for production of economic power. Details of the conceptual design of a 100-Mw(e) reactor and system are discussed. The power cost from a mercury cooled fast breeder reactor was estimated as 21.4 mills/kwh which is competitive with the power cost for the initial Enrico Fermi plant. It was concluded that this reactor concept is technically feasible and has promising long-range economic potential. (M.C.G.)

Battles, D.W.

1960-12-14T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Sediment and radionuclide transport in rivers: radionuclide transport modeling for Cattaraugus and Buttermilk Creeks, New York  

Science Conference Proceedings (OSTI)

SERATRA, a transient, two-dimensional (laterally-averaged) computer model of sediment-contaminant transport in rivers, satisfactorily resolved the distribution of sediment and radionuclide concentrations in the Cattaraugus Creek stream system in New York. By modeling the physical processes of advection, diffusion, erosion, deposition, and bed armoring, SERATRA routed three sediment size fractions, including cohesive soils, to simulate three dynamic flow events. In conjunction with the sediment transport, SERATRA computed radionuclide levels in dissolved, suspended sediment, and bed sediment forms for four radionuclides (/sup 137/Cs, /sup 90/Sr, /sup 239/ /sup 240/Pu, and /sup 3/H). By accounting for time-dependent sediment-radionuclide interaction in the water column and bed, SERATA is a physically explicit model of radionuclide fate and migration. Sediment and radionuclide concentrations calculated by SERATA in the Cattaraugus Creek stream system are in reasonable agreement with measured values. SERATRA is in the field performance phase of an extensive testing program designed to establish the utility of the model as a site assessment tool. The model handles not only radionuclides but other contaminants such as pesticides, heavy metals and other toxic chemicals. Now that the model has been applied to four field sites, including the latest study of the Cattaraugus Creek stream system, it is recommended that a final model be validated through comparison of predicted results with field data from a carefully controlled tracer test at a field site. It is also recommended that a detailed laboratory flume be tested to study cohesive sediment transport, deposition, and erosion characteristics. The lack of current understanding of these characteristics is one of the weakest areas hindering the accurate assessment of the migration of radionuclides sorbed by fine sediments of silt and clay.

Onishi, Y.; Yabusaki, S.B.; Kincaid, C.T.; Skaggs, R.L.; Walters, W.H.

1982-12-01T23:59:59.000Z

362

October 2001 Mercury Report of Earth Engineering Center to New York Academy of Sciences SOURCES AND MATERIAL BALANCE OF MERCURY  

E-Print Network (OSTI)

of mercury from MWC flue gases. After MACT controls reduce total mercury emission rates by 90% or greater not address any chemical transformations affecting mercury in soil, water or sediments (oxidation, reduction Speciation in Flue Gases: Overcoming the Analytical Difficulties," Brooks Rand Ltd., Seattle, WA, Fall 1991

Columbia University

363

Improving Targeted Radionuclide Therapy Using Nuclear Nanotechnology  

E-Print Network (OSTI)

The objectives of this thesis are to produce radioactive antibody-conjugated gold nanoparticles to improve the efficacy of targeted radionuclide therapy for the treatment of cancer, and to demonstrate that this product can be produced at Texas A&M University. We have proposed a method for determining the distribution of radioactive nuclei per nanoparticle, which is critical for determining radiotherapeutic efficacy. Using the distribution of radioactive nuclei per nanoparticle, we have produced methods for calculating the radiative dose to tissue using nano-improved targeted radionuclide therapy, but more importantly we propose procedures to experimentally determine the efficacy of targeted radionuclide therapy improved by application of radioactive nanomaterials in combination with immunotherapy, nanomaterial cytotoxicity, and other cancer therapies such as chemotherapy. These methods can also be used to determine the efficacy of combinatory treatments as a function of time. Characterization of the antibody-nanoparticle attachment is critical; we have demonstrated successful antibody-nanoparticle conjugation using atomic force microscopy, dynamic light scattering, and agarose gel electrophoresis, providing more conclusive evidence of successful conjugation compared to flow cytometry. We provide a mathematical derivation from basic electron-transport principles which demonstrates the theoretical dosimetric advantages of applying radioactive nanomaterials to targeted radionuclide therapy. The general formulae can be applied to any tumor size, any radionuclide, and any pharmacokinetic nanoparticle distribution throughout the body, ultimately allowing a quick method of approximating the necessary activation time and treatment dosage parameters for a specific patient without burdensome Monte Carlo computational simulations. We further demonstrated that nano-TRT dosage to tumors should be considered as a function of radial position rather than average, as the dose across the tumor may be noticeably non-uniform causing some portions of the tumor to receive (potentially) significantly less dose than average.

Evans, Jordan Andrew

2013-05-01T23:59:59.000Z

364

2006 LANL Radionuclide Air Emissions Report  

SciTech Connect

This report describes the impacts from emissions of radionuclides at Los Alamos National Laboratory (LANL) for calendar year 2006. This report fulfills the requirements established by the Radionuclide National Emissions Standards for Hazardous Air Pollutants (Rad-NESHAP). This report is prepared by LANL's Rad-NESHAP compliance team, part of the Environmental Protection Division. The information in this report is required under the Clean Air Act and is being reported to the U.S. Environmental Protection Agency (EPA). The highest effective dose equivalent (EDE) to an off-site member of the public was calculated using procedures specified by the EPA and described in this report. LANL's EDE was 0.47 mrem for 2006. The annual limit established by the EPA is 10 mrem per year. During calendar year 2006, LANL continuously monitored radionuclide emissions at 28 release points, or stacks. The Laboratory estimates emissions from an additional 58 release points using radionuclide usage source terms. Also, LANL uses a network of air samplers around the Laboratory perimeter to monitor ambient airborne levels of radionuclides. To provide data for dispersion modeling and dose assessment, LANL maintains and operates meteorological monitoring systems. From these measurement systems, a comprehensive evaluation is conducted to calculate the EDE for the Laboratory. The EDE is evaluated as any member of the public at any off-site location where there is a residence, school, business, or office. In 2006, this location was the Los Alamos Airport Terminal. The majority of this dose is due to ambient air sampling of plutonium emitted from 2006 clean-up activities at an environmental restoration site (73-002-99; ash pile). Doses reported to the EPA for the past 10 years are shown in Table E1.

David P. Fuehne

2007-06-30T23:59:59.000Z

365

Optimized Parameters for a Mercury Jet Target  

Science Conference Proceedings (OSTI)

A study of target parameters for a high-power, liquid mercury jet target system for a neutrino factory or muon collider is presented. Using the MARS code, we simulate particle production initiated by incoming protons with kinetic energies between 2 and 100 GeV. For each proton beam energy, we maximize production by varying the geometric parameters of the target: the mercury jet radius, the incoming proton beam angle, and the crossing angle between the mercury jet and the proton beam. The number of muons surviving through an ionization cooling channel is determined as a function of the proton beam energy. We optimize the mercury jet target parameters: the mercury jet radius, the incoming proton beam angle and the crossing angle between the mercury jet and the proton beam for each proton beam energy. The optimized target radius varies from about 0.4 cm to 0.6 cm as the proton beam energy increases. The optimized beam angle varies from 75 mrad to 120 mrad. The optimized crossing angle is near 20 mrad for energies above 5 GeV. These values differ from earlier choices of 67 mrad for the beam angle and 33 mrad for the crossing angle. These new choices for the beam parameters increase the meson production by about 20% compared to the earlier parameters. Our study demonstrates that the maximum meson production efficiency per unit proton beam power occurs when the proton kinetic energy is in the range of 5-15 GeV. Finally, the dependence on energy of the number of muons at the end of the cooling channel is nearly identical to the dependence on energy of the meson production 50 m from the target. This demonstrates that the target parameters can be optimized without the additional step of running the distribution through a code such as ICOOL that simulates the bunching, phase rotation, and cooling.

Ding, X.; Kirk, H.

2010-12-01T23:59:59.000Z

366

NETL: IEP - Mercury Emissions Control: Emissions Characterization  

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

Control Control Emissions Characterization In anticipation of the 1990 CAAAs, specifically the draft Title III regarding the characterization of potential HAPs from electric steam generating units, DOE initiated a new Air Toxics Program in 1989. The DOE Mercury Measurement and Control Program evolved as a result of the findings from the comprehensive assessment of hazardous air pollutants studies conducted by DOE from 1990 through 1997. DOE, in collaboration with EPRI, performed stack tests at a number of coal-fired power plants (identified on map below) to accurately determine the emission rates of a series of potentially toxic chemicals. These tests had not been conducted previously because of their cost, about $1 million per test, so conventional wisdom on emissions was based on emission factors derived from analyses of coal. In general, actual emissions were found to be about one-tenth previous estimates, due to a high fraction of the pollutants being captured by existing particulate control systems. These data resulted in a decision by EPA that most of these pollutants were not a threat to the environment, and needed no further regulation at power plants. This shielded the coal-fired power industry from major (tens of millions) costs that would have resulted from further controlling these emissions. However, another finding of these studies was that mercury was not effectively controlled in coal-fired utility boiler systems. Moreover, EPA concluded that a plausible link exists between these emissions and adverse health effects. Ineffective control of mercury by existing control technologies resulted from a number of factors, including variation in coal composition and variability in the form of the mercury in flue gases. The volatility of mercury was the main contributor for less removal, as compared to the less volatile trace elements/metals which were being removed at efficiencies over 99% with the fly ash. In addition, it was determined that there was no reliable mercury speciation method to accurately distinguish between the elemental and oxidized forms of mercury in the flue gas. These two forms of mercury respond differently to removal techniques in existing air pollution control devices utilized by the coal-fired utility industry.

367

MERCURY CONTROL WITH ADVANCED HYBRID PARTICULATE COLLECTOR  

SciTech Connect

This project was awarded under U.S. Department of Energy (DOE) National Energy Technology Laboratory (NETL) Program Solicitation DE-PS26-00NT40769 and specifically addressed Technical Topical Area 4-Testing Novel and Less Mature Control Technologies on Actual Flue Gas at the Pilot Scale. The project team included the Energy & Environmental Research Center (EERC) as the main contractor; W.L. Gore & Associates, Inc., as a technical and financial partner; and the Big Stone Power Plant operated by Otter Tail Power Company, host for the field-testing portion of the research. Since 1995, DOE has supported development of a new concept in particulate control called the advanced hybrid particulate collector (AHPC). The AHPC has been licensed to W.L. Gore & Associates, Inc., and has been marketed as the Advanced Hybrid{trademark} filter by Gore. The Advanced Hybrid{trademark} filter combines the best features of electrostatic precipitators (ESPs) and baghouses in a unique configuration, providing major synergism between the two collection methods, both in the particulate collection step and in the transfer of dust to the hopper. The Advanced Hybrid{trademark} filter provides ultrahigh collection efficiency, overcoming the problem of excessive fine-particle emissions with conventional ESPs, and it solves the problem of reentrainment and re-collection of dust in conventional baghouses. The Advanced Hybrid{trademark} filter also appears to have unique advantages for mercury control over baghouses or ESPs as an excellent gas--solid contactor. The objective of the project was to demonstrate 90% total mercury control in the Advanced Hybrid{trademark} filter at a lower cost than current mercury control estimates. The approach included bench-scale batch tests, larger-scale pilot testing with real flue gas on a coal-fired combustion system, and field demonstration at the 2.5-MW (9000-acfm) scale at a utility power plant to prove scale-up and demonstrate longer-term mercury control. An additional task was included in this project to evaluate mercury oxidation upstream of a dry scrubber by using mercury oxidants. This project demonstrated at the pilot-scale level a technology that provides a cost-effective technique to control mercury and, at the same time, greatly enhances fine particulate collection efficiency. The technology can be used to retrofit systems currently employing inefficient ESP technology as well as for new construction, thereby providing a solution for improved fine particulate control combined with effective mercury control for a large segment of the U.S. utility industry as well as other industries.

Ye Zhuang; Stanley J. Miller

2005-05-01T23:59:59.000Z

368

Enhanced Mercury Removal by Wet FGD Systems  

Science Conference Proceedings (OSTI)

This report provides results from testing conducted in 2005 as part of three EPRI co-funded projects that are aimed at enhancing the capture of mercury in flue gas from coal-fired power boilers when scrubbed by wet flue gas desulfurization (FGD) systems. The first project is co-sponsored by the U.S. Department of Energy's National Energy Technology Laboratory (DOE-NETL) under Cooperative Agreement DE-FC26-01NT41185, "Pilot Testing of Mercury Oxidation Catalysts for Upstream of Wet FGD," as well as by two...

2006-03-07T23:59:59.000Z

369

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

Open Energy Info (EERE)

Mercury Vapor At Haleakala Volcano Area (Thomas, 1986) Mercury Vapor At Haleakala Volcano Area (Thomas, 1986) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Haleakala Volcano Area (Thomas, 1986) Exploration Activity Details Location Haleakala Volcano Area Exploration Technique Mercury Vapor Activity Date Usefulness not indicated DOE-funding Unknown Notes The field survey program on the northwest rift zone consisted of soil mercury and radon emanometry surveys, groundwater temperature and chemistry studies, Schlumberger resistivity soundings and self-potential profiles. Geophysical and geochemical surveys along this rift (southwest) were limited by difficult field conditions and access limitations. The geophysical program consisted of one Schlumberger sounding, one

370

Method for high temperature mercury capture from gas streams  

DOE Patents (OSTI)

A process to facilitate mercury extraction from high temperature flue/fuel gas via the use of metal sorbents which capture mercury at ambient and high temperatures. The spent sorbents can be regenerated after exposure to mercury. The metal sorbents can be used as pure metals (or combinations of metals) or dispersed on an inert support to increase surface area per gram of metal sorbent. Iridium and ruthenium are effective for mercury removal from flue and smelter gases. Palladium and platinum are effective for mercury removal from fuel gas (syngas). An iridium-platinum alloy is suitable for metal capture in many industrial effluent gas streams including highly corrosive gas streams.

Granite, E.J.; Pennline, H.W.

2006-04-25T23:59:59.000Z

371

Sorbents for the oxidation and removal of mercury  

DOE Patents (OSTI)

A promoted activated carbon sorbent is described that is highly effective for the removal of mercury from flue gas streams. The sorbent comprises a new modified carbon form containing reactive forms of halogen and halides. Optional components may be added to increase reactivity and mercury capacity. These may be added directly with the sorbent, or to the flue gas to enhance sorbent performance and/or mercury capture. Mercury removal efficiencies obtained exceed conventional methods. The sorbent can be regenerated and reused. Sorbent treatment and preparation methods are also described. New methods for in-flight preparation, introduction, and control of the active sorbent into the mercury contaminated gas stream are described.

Olson, Edwin S. (Grand Forks, ND); Holmes, Michael J. (Thompson, ND); Pavlish, John H. (East Grand Forks, MN)

2012-05-01T23:59:59.000Z

372

Sorbents for the oxidation and removal of mercury  

DOE Patents (OSTI)

A promoted activated carbon sorbent is described that is highly effective for the removal of mercury from flue gas streams. The sorbent comprises a new modified carbon form containing reactive forms of halogen and halides. Optional components may be added to increase reactivity and mercury capacity. These may be added directly with the sorbent, or to the flue gas to enhance sorbent performance and/or mercury capture. Mercury removal efficiencies obtained exceed conventional methods. The sorbent can be regenerated and reused. Sorbent treatment and preparation methods are also described. New methods for in-flight preparation, introduction, and control of the active sorbent into the mercury contaminated gas stream are described.

Olson, Edwin S. (Grand Forks, ND); Holmes, Michael J. (Thompson, ND); Pavlish, John H. (East Grand Forks, MN)

2008-10-14T23:59:59.000Z

373

Ferrihydrite as an Enterosorbent for Arsenic  

E-Print Network (OSTI)

Arsenic in drinking water is a problem in many developing nations such as Taiwan and Bangladesh. Currently, no oral binding agent exists for the mitigation of arsenic toxicity. The goals of this research were to 1) screen a variety of sorbents for their ability to sorb As from water and screen for potential nutrient interactions with vitamin A (VA) and riboflavin (RF) isotherms; 2) further describe the sorption of As to ferrihydrite using isothermal analysis and a simulated gastrointestinal model (GI), and by testing ferrihydrites ability to protect Hydra from As toxicity; 3) verify ferrihydrites safety and efficacy in a short term rodent model. Ferrihydrite was found to be the most effective sorbent for both As(III) and As(V). Exchanging SWy-2 with sulfur containing organic groups increased the sorption of both As(V) and As(III) compared to the parent clay, though the total As sorbed was much less than As sorption by ferrihydrite. Ferrihydrite and an industrially produced ferrihydrite (IPF) both sorbed As(V) and As(III) with high capacity. Both ferrihydrites also sorbed As(V) and As(III) at high capacity in the simulated GI model. Fe measured in the simulated GI tract was below tolerable daily limits for both ferrihydrite and IPF. Ferrihydrite at 0.25 percent w/w was found to protect Hydra up to 200 times the minimal effective concentration (MEC) for As(III) and over 2.5 times the MEC for As(V), while IPF at 0.25 percent w/w protected Hydra up to 200 times the MEC for As(III) and just over 2 times the MEC for As(V). IPF was apparently safe and well tolerated by the rats in our study over a period of 2 weeks. No statistically significant differences were seen in serum biochemistry, serum Fe, serum VA, or serum vitamin E between rats fed control diet versus those fed 0.5 percent w/w IPF. Ferrihydrite was found to reduce urinary As after a single gavage of 0.5 mL of 500 ppm As(III) or As(V). These results verify in vitro findings and suggest that ferrihydrite is apparently safe and effective as an enterosorbent for As.

Taylor, John Floyd

2010-12-01T23:59:59.000Z

374

A proposed sensor deployment to investigate biogeochemical controls on mercury cycling in Mugu Lagoon, California (CON 5)  

E-Print Network (OSTI)

biogeochemical controls on mercury cycling in Mugu Lagoon,of UCLA, is impaired for mercury, a potent neurotoxin, whichhealth and wildlife t o Mercury methylation is the process

Sarah Rothenberg; Jenny Jay

2006-01-01T23:59:59.000Z

375

Radionuclide Interaction and Transport in Representative Geologic Media |  

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

Radionuclide Interaction and Transport in Representative Geologic Radionuclide Interaction and Transport in Representative Geologic Media Radionuclide Interaction and Transport in Representative Geologic Media The report presents information related to the development of a fundamental understanding of disposal-system performance in a range of environments for potential wastes that could arise from future nuclear fuel cycle alternatives. It addresses selected aspects of the development of computational modeling capability for the performance of storage and disposal options. Topics include radionuclide interaction with geomedia, colloid-facilitated radionuclide transport (Pu colloids), interaction between iodide (accumulate in the interlayer regions of clay minerals) and a suite of clay minerals, adsorption of uranium onto granite and bentonite,

376

Mercury in mussels of Bellingham Bay, Washington, (USA)  

SciTech Connect

Laboratory experiments demonstrated the existence of metallothionein-like, low molecular weight, mercury-binding proteins in the marine mussel Mytilus edulis. Relatively large quantities of mercury were associated with such proteins in gills and digestive gland, the organs of interest in the present study. /sup 14/C-incorporation indicated induction of the protein in gills, but not in digestive gland. Mercury in digestive gland may have bound to existing metal-binding proteins. Short-term incorporation of mercury occurred primarily in gills. The induction of mercury-binding proteins in gills may have facilitated detoxification of mercury at the site of uptake. Mercury in mussels of Bellingham Bay were shown to have decreased from 1970 to 1978, the collection date for the present study. Mercury levels were low but approximately three times higher than those from uncontaminated areas. Mercury associated with the mercury-binding protein of gills and digestive glands of Bellingham Bay mussels were low and reflected the concentrations measured in the whole tissues. However, the highest concentration of mercury was associated with the low molecular pool components, the identity of which is not presently known.

Roesijadi, G.; Drum, A.S.; Bridge, J.R.

1978-11-01T23:59:59.000Z

377

LFCM (liquid-fed ceramic melter) processing characteristics of mercury  

SciTech Connect

An experimental-scale liquid-fed ceramic melter was used in a series of tests to evaluate the processing characteristics of mercury in simulated defense waste under various melter operating conditions. This solidification technology had no detectable capacity for incorporating mercury into its borosilicate, vitreous, product, and essentially all the mercury fed to the melter was lost to the off-gas system as gaseous effluent. An ejector venturi scrubber condensed and collected 97% of the mercury evolved from the melter. Chemically the condensed mercury effluent was composed entirely of chlorides, and except in a low-temperature test, mercury chlorides (Hg{sub 2}Cl{sub 2}) was the primary chloride formed. As a result, combined mercury accounted for most of the insoluble mass collected by the process quench scrubber. Although macroscopic quantities of elemental mercury were never observed in process secondary waste streams, finely divided and dispersed mercury that blackened all condensed Hg{sub 2}Cl{sub 2} residues was capable of saturating the quenched process exhaust with mercury vapor. However, the vapor pressure of mercury in the quenched melter exhaust was easily and predictably controlled with an off-gas stream chiller. 5 refs., 4 figs., 12 tabs.

Goles, R.W.; Sevigny, G.J.; Andersen, C.M.

1990-06-01T23:59:59.000Z

378

FY09 assessment of mercury reduction at SNL/NM.  

Science Conference Proceedings (OSTI)

This assessment takes the result of the FY08 performance target baseline of mercury at Sandia National Laboratories/New Mexico, and records the steps taken in FY09 to collect additional data, encourage the voluntary reduction of mercury, and measure success. Elemental (metallic) mercury and all of its compounds are toxic, and exposure to excessive levels can permanently damage or fatally injure the brain and kidneys. Elemental mercury can also be absorbed through the skin and cause allergic reactions. Ingestion of inorganic mercury compounds can cause severe renal and gastrointestinal damage. Organic compounds of mercury such as methyl mercury, created when elemental mercury enters the environment, are considered the most toxic forms of the element. Exposures to very small amounts of these compounds can result in devastating neurological damage and death.1 SNL/NM is required to report annually on the site wide inventory of mercury for the Environmental Protection Agency's (EPA) Toxics Release Inventory (TRI) Program, as the site's inventory is excess of the ten pound reportable threshold quantity. In the fiscal year 2008 (FY08) Pollution Prevention Program Plan, Section 5.3 Reduction of Environmental Releases, a performance target stated was to establish a baseline of mercury, its principle uses, and annual quantity or inventory. This was accomplished on July 29, 2008 by recording the current status of mercury in the Chemical Information System (CIS).

McCord, Samuel Adam

2010-02-01T23:59:59.000Z

379

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

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

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

380

NETL: News Release - Innovative Mercury Removal Technique Shows Early  

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

August 5, 2003 August 5, 2003 Innovative Mercury Removal Technique Shows Early Promise Photochemical Process Developed in Federal Lab Removes Mercury from Flue Gas - NETL scientist Evan Granite prepares a lab test of the UV mercury removal process. - NETL scientist Evan Granite prepares for a lab test of the UV mercury removal process. MORGANTOWN, WV - A promising technology to remove mercury from coal-fired power plants -- dubbed the "GP-254 Process" -- has been developed and is currently being tested at the Department of Energy's National Energy Technology Laboratory (NETL). Newly patented, the GP-254 Process enhances mercury removal using ultraviolet light to induce various components of power plant stack gas to react with the mercury, and changes the

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381

NETL: Mercury Emissions Control Technologies - Bench Scale Kinetics of  

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

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

382

NETL: Mercury Emissions Control Technologies - Development of Comprehensive  

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

Full-Scale Testing of Mercury Control Via Sorbent Injection Full-Scale Testing of Mercury Control Via Sorbent Injection DOE has identified technologies (based on past DOE and other R&D organizations' mercury measurement and control achievements) that are expected to be important in developing possible strategies on mercury control for the coal-fired electric utility industry. To address critical questions related to cost and efficiency of these mercury control technologies, DOE has funded the first of a kind large-scale initiative aimed at testing and evaluating large-scale mercury control technologies for coal-based power systems. These tests will collect cost and performance data with parametric and long term field experiments at power plants with existing air pollution control devices (APCDs) utilized to control other pollutants as well as mercury in hopes of providing the cheapest control options for the utility industry in mid-term application (5 to 10 years).

383

Mercury Handling for the Target System for a Muon Collider  

Science Conference Proceedings (OSTI)

The baseline target concept for a Muon Collider or Neutrino Factory is a free-stream mercury jet being impacted by an 8-GeV proton beam. The target is located within a 20-T magnetic field, which captures the generated pions that are conducted to a downstream decay channel. Both the mercury and the proton beam are introduced at slight downward angles to the magnetic axis. A pool of mercury serves as a receiving reservoir for the mercury and a dump for the unexpended proton beam. The impact energy of the remaining beam and jet are substantial, and it is required that splashes and waves be controlled in order to minimize the potential for interference of pion production at the target. Design issues discussed in this paper include the nozzle, splash mitigation in the mercury pool, the mercury containment vessel, and the mercury recirculation system.

Graves, Van B [ORNL; Mcdonald, K [Princeton University; Kirk, H. [Brookhaven National Laboratory (BNL); Weggel, Robert [Particle Beam Laser, Inc.; Souchlas, Nicholas [Particle Beam Laser, Inc.; Sayed, H [Brookhaven National Laboratory (BNL); Ding, X [University of California, Los Angeles

2012-01-01T23:59:59.000Z

384

Radionuclide behavior in water saturated porous media: Diffusion and infiltration coupling of thermodynamically and kinetically controlled radionuclide water - mineral interactions  

SciTech Connect

A model is developed describing one dimensional radionuclide transport in porous media coupled with locally reversible radionuclide water-mineral exchange reactions and radioactive decay. Problems are considered in which radionuclide transport by diffusion and infiltration processes occur in cases where radionuclide water-solid interaction are kinetically and thermodynamically controlled. The limits of Sr-90 and Cs-137 migration are calculated over a wide range of the problem variables (infiltration velocity, distribution coefficients, and rate constants of water-mineral radionuclide exchange reactions).

Spasennykh, M.Yu. [Vernadsky Institute of Geochemistry and Analytical Chemistry, Moscow (Russian Federation); Apps, J.A. [Lawrence Berkeley Lab., CA (United States)

1995-05-01T23:59:59.000Z

385

Application of chemical kinetics to mercury cycling in the aquatic environment: Photoreduction of mercury(II) and binding of mercury(II) and methylmercury(+) to natural ligands .  

E-Print Network (OSTI)

??The thesis comprises four main chapters on chemical reactions and kinetics of some of the processes involved in the global mercury cycle. In the first (more)

Ababneh, Fuad A

2013-01-01T23:59:59.000Z

386

NETL: IEP - Mercury Emissions Control: Regulatory Drivers  

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

Regulatory Drivers Regulatory Drivers The Clean Air Act Amendments of 1990 (CAAA) brought about new awareness regarding the overall health-effects of stationary source fossil combustion emissions. Title III of the CAAA identified 189 pollutants, including mercury, as hazardous or toxic and required the Environmental Protection Agency (EPA) to evaluate their emissions by source, health effects and environmental implications, including the need to control these emissions. These pollutants are collectively referred to as air toxics or hazardous air pollutants (HAPs). The provisions in Title III specific to electric generating units (EGU) were comprehensively addressed by DOE's National Energy Technology Laboratory (NETL) and the Electric Power Research Institute (EPRI) in collaborative air toxic characterization programs conducted between 1990 and 1997. This work provided most of the data supporting the conclusions found in EPA's congressionally mandated reports regarding air toxic emissions from coal-fired utility boilers; the Mercury Study Report to Congress (1997)1 and the "Study of Hazardous Air Pollutant Emissions from Electric Utility Steam Generating Units -- Final Report to Congress" (1998).2 The first report identified coal-fired power plants as the largest source of human-generated mercury emissions in the U.S. and the second concluded that mercury from coal-fired utilities was the HAP of "greatest potential concern" to the environment and human health that merited additional research and monitoring.

387

Catalytic Reactor For Oxidizing Mercury Vapor  

DOE Patents (OSTI)

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

Helfritch, Dennis J. (Baltimore, MD)

1998-07-28T23:59:59.000Z

388

Coal Biomodification to Reduce Mercury Emissions  

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

Road P.O. Box 880 Morgantown, WV 26507-0880 304-285-4132 heino.beckert@netl.doe.gov Coal BiomodifiCation to ReduCe meRCuRy emissions Description In partnership with a number of...

389

Impacts of NOx Controls on Mercury Controllability  

Science Conference Proceedings (OSTI)

Past tests have led researchers and air pollution regulators to hypothesize that nitrogen oxides (NOx) controls can enhance mercury capture by particulate collection devices and sulfur dioxide (SO2) scrubbers. This technology review presents results obtained to date from a comprehensive program designed to confirm, qualify, and quantify these hypotheses.

2002-03-13T23:59:59.000Z

390

Evaluation of Sorbent Injection for Mercury Control  

Science Conference Proceedings (OSTI)

ADA-ES, Inc., with support from DOE/NETL, EPRI, and industry partners, studied mercury control options at six coal-fired power plants. The overall objective of the this test program was to evaluate the capabilities of activated carbon injection at six plants: Sunflower Electric's Holcomb Station Unit 1, AmerenUE's Meramec Station Unit 2, Missouri Basin Power Project's Laramie River Station Unit 3, Detroit Edison's Monroe Power Plant Unit 4, American Electric Power's Conesville Station Unit 6, and Labadie Power Plant Unit 2. These plants have configurations that together represent 78% of the existing coal-fired generation plants. The financial goals for the program established by DOE/NETL were to reduce the uncontrolled mercury emissions by 50 to 70% at a cost 25 to 50% lower than the target established by DOE of $60,000 per pound of mercury removed. Results from testing at Holcomb, Laramie, Meramec, Labadie, and Monroe indicate the DOE goal was successfully achieved. However, further improvements for plants with conditions similar to Conesville are recommended that would improve both mercury removal performance and economics.

Sharon Sjostrom

2008-06-30T23:59:59.000Z

391

Bioremediation of Metals and Radionuclides: What It Is and How It Works (2nd Edition)  

Science Conference Proceedings (OSTI)

This primer is intended for people interested in environmental problems of the U.S. Department of Energy (DOE) and in their potential solutions. It will specifically look at some of the more hazardous metal and radionuclide contaminants found on DOE lands and at the possibilities for using bioremediation technology to clean up these contaminants. The second edition of the primer incorporates recent findings by researchers in DOE's Natural and Accelerated Bioremediation Research (NABIR) Program. Bioremediation is a technology that can be used to reduce, eliminate, or contain hazardous waste. Over the past two decades, it has become widely accepted that microorganisms, and to a lesser extent plants, can transform and degrade many types of contaminants. These transformation and degradation processes vary, depending on the physical-chemical environment, microbial communities, and nature of the contaminant. This technology includes intrinsic bioremediation, which relies on naturally occurring processes, and accelerated bioremediation, which enhances microbial degradation or transformation through the addition of nutrients (biostimulation) or inoculation with microorganisms (bioaugmentation). Over the past few years, interest in bioremediation has increased. It has become clear that many organic contaminants such as hydrocarbon fuels can be degraded to relatively harmless products such as CO{sub 2} (the end result of the degradation process). Waste water managers and scientists have also found that microorganisms can interact with metals and convert them from one chemical form to another. Laboratory tests and ex situ bioremediation applications have shown that microorganisms can change the valence, or oxidation state, of some heavy metals (e.g., chromium and mercury) and radionuclides (e.g., uranium) by using them as electron acceptors. In some cases, the solubility of the altered species decreases and the contaminant is immobilized in situ, i.e., precipitated into an insoluble salt in the sediment. In other cases, the opposite occurs--the solubility of the altered species increases, increasing the mobility of the contaminant and allowing it to be more easily flushed from the environment. Both of these kinds of transformations present opportunities for bioremediation of metals and radionuclides--either to lock them in place, or to accelerate their removal. DOE's goal is to reduce the risk and related exposure to ground water, sediment, and soil contamination at Department of Energy facilities. Subsurface bioremediation of metals and radionuclides at the site of contamination (in situ bioremediation) is not yet in widespread use. However, successful in situ applications of bioremediation to petroleum products and chlorinated solvents provide experience from which scientists can draw. Taken together, the accomplishments in these areas have led scientists and engineers to be optimistic about applying this technology to the mixtures of metals and radionuclides that are found at some of the most contaminated DOE sites. This primer examines some of the basic microbial and chemical processes that are a part of bioremediation, specifically the bioremediation of metals and radionuclides. The primer is divided into six sections, with the information in each building on that of the previous. The sections include features that highlight topics of interest and provide background information on specific biological and chemical processes and reactions. The first section briefly examines the scope of the contamination problem at DOE facilities. The second section gives a summary of some of the most commonly used bioremediation technologies, including successful in situ and ex situ techniques. The third discusses chemical and physical properties of metals and radionuclides found in contaminant mixtures at DOE sites, including solubility and the most common oxidation states in which these materials are found. The fourth section is an overview of the basic microbial processes that occur in bioremediation. The fifth section looks at specific in s

Palmisano, Anna; Hazen, Terry

2003-09-30T23:59:59.000Z

392

Evaluation of Sorbent Injection for Mercury Control  

SciTech Connect

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

Sharon Sjostrom

2006-04-30T23:59:59.000Z

393

Effect of pressure on arsenic diffusion in germanium  

SciTech Connect

We report preliminary results of a study of the activation volume for diffusion of arsenic in germanium. High-temperature high-pressure anneals were performed in a liquid argon pressure medium in a diamond anvil cell capable of reaching 5 GPa and 750 C,l which is externally heated for uniform and repeatable temperature profiles. Broadening of an ion-implanted arsenic profile was measured by Secondary Ion Mass Spectrometry. Hydrostatic pressure retards the diffusivity at 575 C, characterized by an activation volume that is +15% of the atomic volume of Ge. Implications for diffusion mechanisms are discussed.

Mitha, S.; Theiss, S.D.; Aziz, M.J. [Harvard Univ., Cambridge, MA (United States); Schiferl, D. [Los Alamos National Lab., NM (United States); Poker, D.B. [Oak Ridge National Lab., TN (United States)

1994-01-01T23:59:59.000Z

394

Arsenic and Selenium Speciation in Fly Ash and Wastewater  

Science Conference Proceedings (OSTI)

The objective of the work is to predict As and Se behavior in pond wastewater based on coal and power plant characteristics so that utilities will have tools for selection of coals (and blends) that will allow them to meet applicable water quality regulations in the ash pond discharge. Arsenic and selenium were chosen as the focus of this work because the behavior of arsenic and selenium is not well correlated with pH in ash pond water, but with speciation of these oxyanions in the fly ash. Furthermore, ...

2005-03-28T23:59:59.000Z

395

ORIGINAL ARTICLE Radionuclide Concentrations in Benthic Invertebrates  

Office of Legacy Management (LM)

Environ Monit Assess (2007) 128:329-341 Environ Monit Assess (2007) 128:329-341 DO1 10.1007/~10661-006-93 I 6 4 ORIGINAL ARTICLE - Radionuclide Concentrations in Benthic Invertebrates from Amchitka and Kiska Islands in the Aleutian Chain, Alaska Joanna Burger Michael Gochfeld Stephen C. Jewett Received: 8 March 2006 /Accepted: 8 May 2006 1 Published online: 21 October 2006 0 Springer Science + Business Media B.V. 2006 Abstract Concentrations of 13 radionuclides 1291, 60co, 1 5 2 ~ ~ , 9 0 s r , 9 9 ~ ~ , 2 4 1 ~ ~ , 238pu, 239249pu, 2 3 4 ~ , 2 3 5 ~ , 236U, 2 3 8 ~ were examined in seven species of invertebrates from Amchitka and Kiska Islands, in the Aleutian Chain of Alaska, using gamma spectroscopy, inductively coupled plasma mass spectroscopy, and alpha spectroscopy. Amchitka Island was the site of three underground nuclear test

396

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

397

Radionuclide transport in the Yenisei River  

E-Print Network (OSTI)

Data characterizing the pollution of the Yenisei River (water and bottom sediment) by radionuclide resulting from the use of the river water for cooling industrial reactors in the Mining-Chemical Complex are presented. Studies have been made of the contamination of the river during the period when reactors with direct flow cooling were used and after these were shut down. Distinctive features of the migration of radionuclide in the Yenisei are noted, in particular, their distribution between the solid and liquid phases. The amounts of 137Cs, 65Zn, 60Co, 54Mn, and 152Eu in the channel are determined from the effluent discharge site to Dudinka port. The rate of continuous self removal of 137Cs is estimated to be 0.19 1/year, corresponding to a half purification time of 3.6 years for a 600 km long segment of the river bed.

S. M. Vakulovsky; E. G. Tertyshnik; A. I. Kabanov

2012-11-15T23:59:59.000Z

398

Radionuclide Air Emission Report for 2008  

SciTech Connect

Berkeley Lab operates facilities where radionuclides are handled and stored. These facilities are subject to the U.S. Environmental Protection Agency (EPA) radioactive air emission regulations in Code of Federal Regulations (CFR) Title 40, Part 61, Subpart H (EPA 1989). Radionuclides may be emitted from stacks or vents on buildings where radionuclide production or use is authorized or they may be emitted as diffuse sources. In 2008, all Berkeley Lab sources were minor sources of radionuclides (sources resulting in a potential dose of less than 0.1 mrem/yr [0.001 mSv/yr]). These minor sources include more than 100 stack sources and one source of diffuse emissions. There were no unplanned emissions from the Berkeley Lab site. Emissions from minor sources (stacks and diffuse emissions) either were measured by sampling or monitoring or were calculated based on quantities used, received for use, or produced during the year. Using measured and calculated emissions, and building-specific and common parameters, Laboratory personnel applied the EPA-approved computer code, CAP88-PC, to calculate the effective dose equivalent to the maximally exposed individual (MEI). The effective dose equivalent from all sources at Berkeley Lab in 2008 is 5.2 x 10{sup -3} mrem/yr (5.2 x 10{sup -5} mSv/yr) to the MEI, well below the 10 mrem/yr (0.1 mSv/yr) dose standard. The location of the MEI is at the University of California (UC) Lawrence Hall of Science, a public science museum about 1500 ft (460 m) east of Berkeley Lab's Building 56. The estimated collective effective dose equivalent to persons living within 50 mi (80 km) of Berkeley Lab is 1.1 x 10{sup -1} person-rem (1.1 x 10{sup -3} person-Sv) attributable to the Lab's airborne emissions in 2008.

Wahl, Linnea

2009-05-21T23:59:59.000Z

399

Radionuclide Air Emission Report for 2007  

Science Conference Proceedings (OSTI)

Berkeley Lab operates facilities where radionuclides are handled and stored. These facilities are subject to the U.S. Environmental Protection Agency (EPA) radioactive air emission regulations in Code of Federal Regulations (CFR) Title 40, Part 61, Subpart H (EPA 1989). The EPA regulates radionuclide emissions that may be released from stacks or vents on buildings where radionuclide production or use is authorized or that may be emitted as diffuse sources. In 2007, all Berkeley Lab sources were minor stack or building emissions sources of radionuclides (sources resulting in a potential dose of less than 0.1 mrem/yr [0.001 mSv/yr]), there were no diffuse emissions, and there were no unplanned emissions. Emissions from minor sources either were measured by sampling or monitoring or were calculated based on quantities received for use or produced during the year. Using measured and calculated emissions, and building-specific and common parameters, Laboratory personnel applied the EPA-approved computer code, CAP88-PC, Version 3.0, to calculate the effective dose equivalent to the maximally exposed individual (MEI). The effective dose equivalent from all sources at Berkeley Lab in 2007 is 1.2 x 10{sup -2} mrem/yr (1.2 x 10{sup -4} mSv/yr) to the MEI, well below the 10 mrem/yr (0.1 mSv/yr) EPA dose standard. The location of the MEI is at the University of California (UC) Lawrence Hall of Science, a public science museum about 1500 ft (460 m) east of Berkeley Lab's Building 56. The estimated collective effective dose equivalent to persons living within 50 mi (80 km) of Berkeley Lab is 3.1 x 10{sup -1} person-rem (3.1 x 10{sup -3} person-Sv) attributable to the Lab's airborne emissions in 2007.

Wahl, Linnea; Wahl, Linnea

2008-06-13T23:59:59.000Z

400

Radionuclide Air Emission Report for 2009  

SciTech Connect

Berkeley Lab operates facilities where radionuclides are handled and stored. These facilities are subject to the EPA radioactive air emission regulations in 40CFR61, Subpart H (EPA 1989). Radionuclides may be emitted from stacks or vents on buildings where radionuclide production or use is authorized or they may be emitted as diffuse sources. In 2009, all Berkeley Lab sources were minor sources of radionuclides (sources resulting in a potential dose of less than 0.1 mrem/yr [0.001 mSv/yr]). These minor sources included more than 100 stack sources and one source of diffuse emissions. There were no unplanned emissions from the Berkeley Lab site. Emissions from minor sources (stacks and diffuse emissions) either were measured by sampling or monitoring or were calculated based on quantities used, received for use, or produced during the year. Using measured and calculated emissions, and building-specific and common parameters, Laboratory personnel applied the EPA-approved computer code, CAP88-PC, to calculate the effective dose equivalent to the maximally exposed individual (MEI). The effective dose equivalent from all sources at Berkeley Lab in 2009 is 7.0 x 10{sup -3} mrem/yr (7.0 x 10{sup -5} mSv/yr) to the MEI, well below the 10 mrem/yr (0.1 mSv/yr) dose standard. The location of the MEI is at the University of California (UC) Lawrence Hall of Science, a public science museum about 1500 ft (460 m) east of Berkeley Lab's Building 56. The estimated collective effective dose equivalent to persons living within 50 mi (80 km) of Berkeley Lab is 1.5 x 10{sup -1} person-rem (1.5 x 10{sup -3} person-Sv) attributable to the Lab's airborne emissions in 2009.

Wahl, Linnea

2010-06-01T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Oxidation and methylation of dissolved elemental mercury by anaerobic bacteria  

Science Conference Proceedings (OSTI)

Methylmercury is a neurotoxin that poses significant health risks to humans. Some anaerobic sulphate- and iron-reducing bacteria can methylate oxidized forms of mercury, generating methylmercury1-4. One strain of sulphate-reducing bacteria (Desulfovibrio desulfuricans ND132) can also methylate elemental mercury5. The prevalence of this trait among different bacterial strains and species remains unclear, however. Here, we compare the ability of two strains of the sulphate-reducing bacterium Desulfovibrio and one strain of the iron-reducing bacterium Geobacter to oxidise and methylate elemental mercury in a series of laboratory incubations. Experiments were carried out under dark, anaerobic conditions, in the presence of environmentally-relevant concentrations of elemental mercury. We report differences in the ability of these organisms to oxidise and methylate elemental mercury. In line with recent findings5, we show that Desulfovibrio desulfuricans ND132 can both oxidise and methylate elemental mercury. However, the rate of methylation of elemental mercury is only about one third the rate of methylation of oxidized mercury. We also show that Desulfovibrio alaskensis G20 can oxidise, but not methylate, elemental mercury. Geobacter sulfurreducens PCA is able to oxidise and methylate elemental mercury in the presence of cysteine. We suggest that the activity of methylating and non-methylating bacteria may together enhance the formation of methylmercury in anaerobic environments.

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

2013-01-01T23:59:59.000Z

402

Mercury Control with Calcium-Based Sorbents and Oxidizing Agents  

SciTech Connect

This Final Report contains the test descriptions, results, analysis, correlations, theoretical descriptions, and model derivations produced from many different investigations performed on a project funded by the U.S. Department of Energy, to investigate calcium-based sorbents and injection of oxidizing agents for the removal of mercury. Among the technologies were (a) calcium-based sorbents in general, (b) oxidant-additive sorbents developed originally at the EPA, and (c) optimized calcium/carbon synergism for mercury-removal enhancement. In addition, (d) sodium-tetrasulfide injection was found to effectively capture both forms of mercury across baghouses and ESPs, and has since been demonstrated at a slipstream treating PRB coal. It has been shown that sodium-tetrasulfide had little impact on the foam index of PRB flyash, which may indicate that sodium-tetrasulfide injection could be used at power plants without affecting flyash sales. Another technology, (e) coal blending, was shown to be an effective means of increasing mercury removal, by optimizing the concentration of calcium and carbon in the flyash. In addition to the investigation and validation of multiple mercury-control technologies (a through e above), important fundamental mechanism governing mercury kinetics in flue gas were elucidated. For example, it was shown, for the range of chlorine and unburned-carbon (UBC) concentrations in coal-fired utilities, that chlorine has much less effect on mercury oxidation and removal than UBC in the flyash. Unburned carbon enhances mercury oxidation in the flue gas by reacting with HCl to form chlorinated-carbon sites, which then react with elemental mercury to form mercuric chloride, which subsequently desorbs back into the flue gas. Calcium was found to enhance mercury removal by stabilizing the oxidized mercury formed on carbon surfaces. Finally, a model was developed to describe these mercury adsorption, desorption, oxidation, and removal mechanisms, including the synergistic enhancement of mercury removal by calcium.

Thomas K. Gale

2005-07-01T23:59:59.000Z

403

The Effect of Wildfire on Soil Mercury Concentrations in Southern California Watersheds  

E-Print Network (OSTI)

G. J. (2007). Release of mercury from Rocky Mountain forestSlemr, F. (2001). Gaseous mercury emissions from a fire inMontesdeoca, M. R. (2008). Mercury transport in response to

2010-01-01T23:59:59.000Z

404

Contribution of Iron-Reducing Bacteria to Mercury Methylation in Marine Sediments  

E-Print Network (OSTI)

AND R. P. MASON. 2006. Mercury methylation by dissimilatoryPRUCHA, AND G. MIERLE. 1991. Mercury methylation by sulfate-AND J. M. SIEBURTH. 1993. Mercury biogeochemical cycling in

Fleming, Emily J.; Nelson, D C

2006-01-01T23:59:59.000Z

405

ROTATION OF MERCURY: THEORETICAL ANALYSIS OF THE DYNAMICS OF A RIGID ELLIPSOIDAL PLANET  

E-Print Network (OSTI)

Laboratory ROTATION OF MERCURY: THEDRETICAL ANALYSIS OF THEW -7405-eng-48 ROTATION OF MERCURY: THEORETICAL ANALYSIS OFfor the rotation of Mercury is sho'ln to imply locked-in

Laslett, L. Jackson

2008-01-01T23:59:59.000Z

406

USE OF ZEEMAN ATOMIC ABSORPTION SPECTROSCOPY FOR THE MEASUREMENT OF MERCURY IN OIL SHALE GASES  

E-Print Network (OSTI)

and R. E. Poulson. Mercury Emissions From A Simulated In-for the Measurement of Mercury in Oil Shale Gases D. GirvinJFOR THE MEASUREMENT OF MERCURY IN OIL SHALE GASES D. C.

Girvin, D.G.

2011-01-01T23:59:59.000Z

407

A Solid-State 199Hg NMR Study of Mercury Halides  

E-Print Network (OSTI)

red polymorph) suggest that the mercury is in sites of cubicTable III. NMR Properties of Mercury Halide Nuclei a IsotopeState 199 Hg NMR Study of Mercury Halides R. E. Taylor 1 *,

Taylor, Robert E; Bai, Shi; Dybowski, Cecil

2011-01-01T23:59:59.000Z

408

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

409

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

410

Mercury, Cadmium and Lead Biogeochemistry in the SoilPlantInsect System in Huludao City  

E-Print Network (OSTI)

YE, Ketris MP (2005a) Mercury in coal: a review part 1of total and methyl mercury by arthropods. Bull Environ259 DOI 10.1007/s00128-009-9688-6 Mercury, Cadmium and Lead

Zhang, Zhong-Sheng; Lu, Xian-Guo; Wang, Qi-Chao; Zheng, Dong-Mei

2009-01-01T23:59:59.000Z

411

MERCURY EMISSIONS FROM A SIMULATED IN-SITU OIL SHALE RETORT  

E-Print Network (OSTI)

M. and Chang, B. , 1974; Mercury Monitor for Ambient Air,E. Poulson INTRODUCTION Mercury emissions from fossil-fuelHarley, R. A. , 1973; Mercury Balance on a Large Pulverized

Fox, J. P.

2012-01-01T23:59:59.000Z

412

Mercury and Methylmercury in the San Francisco Bay area: land-use impact and indicators  

E-Print Network (OSTI)

R.P. , and Flegal A. R. 2003, Mercury speciation in the SanAbdrashitova S. A. , 2001, Mercury in Aquatic Environment: A222 Hydrology for Planner Mercury and Methylmercury in the

Kim, Hyojin

2008-01-01T23:59:59.000Z

413

Evaluation of MerCAP^TM for Power Plant Mercury Control  

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

Evaluation of MErCaP(tm) for PowEr Plant MErCury Control Background Several technologies are under development for removing mercury from power plant flue gas streams. The mercury...

414

Information on the Fate of Mercury From Fluorescent Lamps Disposed in Landfills  

Science Conference Proceedings (OSTI)

Mercury is contained in energy-efficient fluorescent, mercury-vapor, metal halide, and high-pressure sodium lamps. This report presents information on the potential for air and groundwater contamination when mercury lamps are disposed in municipal landfills.

1995-04-19T23:59:59.000Z

415

CHLORIDE, IN CALCIUM, IN pH ARSENIC, IN  

E-Print Network (OSTI)

LITER PHAST--A Program for Simulating Ground-Water Flow, Solute Transport, and Multicomponent;COVER ILLUSTRATION: Results of PHAST simulation of the evolution of water chemistry in the CentralH ARSENIC, IN MILLIGRAMS PER LITER MILLIGRAMS PER LITER MICROGRAMS PER LITER #12;PHAST--A Program

416

Comment on "Arsenic Mobility and Groundwater Extraction in  

E-Print Network (OSTI)

recharge. A re- cent report from the International Atomic Energy Agency (8) lists eight samples to unprecedented levels starting in the 1950s because of atmospheric testing of nuclear bombs (5). The penetration, this would mean bomb-produced 14 C should have penetrated at least to the depth of maximum arsenic

van Geen, Alexander

417

Limited Temporal Variability of Arsenic Concentrations in 20 Wells  

E-Print Network (OSTI)

Limited Temporal Variability of Arsenic Concentrations in 20 Wells Monitored for 3 Years switched their water consumption to wells that meet the local standard for As in drinking water of 50 µg if As concentrations in those wells could change over time. To address this issue, we report here precise groundwater

van Geen, Alexander

418

Arsenic pilot plant operation and results:Weatherford, Oklahoma.  

SciTech Connect

Narasimhan Consulting Services, Inc. (NCS), under a contract with the Sandia National Laboratories (SNL), designed and operated pilot scale evaluations of the adsorption and coagulation/filtration treatment technologies aimed at meeting the recently revised arsenic maximum contaminant level (MCL) for drinking water. The standard of 10 {micro}g/L (10 ppb) is effective as of January 2006. The pilot demonstration is a project of the Arsenic Water Technology Partnership program, a partnership between the American Water Works Association Research Foundation (AwwaRF), SNL and WERC (A Consortium for Environmental Education and Technology Development). The pilot evaluation was conducted at Well 30 of the City of Weatherford, OK, which supplies drinking water to a population of more than 10,400. Well water contained arsenic in the range of 16 to 29 ppb during the study. Four commercially available adsorption media were evaluated side by side for a period of three months. Both adsorption and coagulation/filtration effectively reduced arsenic from Well No.30. A preliminary economic analysis indicated that adsorption using an iron oxide media was more cost effective than the coagulation/ filtration technology.

Aragon, Malynda Jo; Arora, H. (Narasimhan Consulting Services Inc., Phoenix, Arizona); Karori, Saqib (Narasimhan Consulting Services Inc., Phoenix, Arizona); Pathan, Sakib (Narasimhan Consulting Services Inc., Phoenix, Arizona)

2007-05-01T23:59:59.000Z

419

Tuesday, November 6, 2007 Arsenic Status in Delaware Soils.  

E-Print Network (OSTI)

Tuesday, November 6, 2007 186-4 Arsenic Status in Delaware Soils. Jennifer Seiter, University of Delaware, 531 South College Ave, Rm 152, Department of Plant & Soil Sciences, Newark, DE 19717 & Soil Sciences, Newark, DE 19717-1303. The Delmarva Peninsula is one of the most concentrated poultry

Sparks, Donald L.

420

Oxidation of Mercury in Products of Coal Combustion  

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

Heng Ban Heng Ban Principal Investigator University of Alabama at Birmingham 1150 10th Avenue South Birmingham, AL 35294-4461 205-934-0011 hban@uab.edu Environmental and Water Resources OxidatiOn Of Mercury in PrOducts Of cOal cOMbustiOn Background The 2005 Clean Air Mercury Rule will require significant reductions in mercury emissions from coal-fired power plants. A variety of mercury reduction technologies are under commercial development, but an improved understanding of the fundamental chemical mechanisms that control the transformations and capture of mercury in boilers and pollution control devices is required to achieve necessary performance and cost reduction levels. Oxidized mercury is more easily captured by pollution control devices, such as Selective

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

Mercury Control Technologies for Electric Utilities Burning Lignite Coal  

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

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

422

Mercury Energy formerly Aquus Energy | Open Energy Information  

Open Energy Info (EERE)

Energy formerly Aquus Energy Energy formerly Aquus Energy Jump to: navigation, search Name Mercury Energy (formerly Aquus Energy) Place New Rochelle, New York Zip 10801 Sector Solar Product Integrator of solar energy systems for commercial and residential clients located in the mid-Atlantic and Northeast regions of the US through its wholly-owned subsidary Mercury Solar Energy. References Mercury Energy (formerly Aquus Energy)[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. Mercury Energy (formerly Aquus Energy) is a company located in New Rochelle, New York . References ↑ "Mercury Energy (formerly Aquus Energy)" Retrieved from "http://en.openei.org/w/index.php?title=Mercury_Energy_formerly_Aquus_Energy&oldid=348731

423

Evaluation of the Mercury Soil Mapping Geothermal Exploration Techniques |  

Open Energy Info (EERE)

Evaluation of the Mercury Soil Mapping Geothermal Exploration Techniques Evaluation of the Mercury Soil Mapping Geothermal Exploration Techniques Jump to: navigation, search OpenEI Reference LibraryAdd to library Conference Paper: Evaluation of the Mercury Soil Mapping Geothermal Exploration Techniques Abstract In order to evaluate the suitability of the soil mercury geochemical survey as a geothermal exploration technique, soil concentrates of mercy are compared to the distribution of measured geothermal gradients at Dixie Valley, Nevada; Roosevelt Hot Springs, Utah; and Nova, Japan. Zones containing high mercury values are found to closely correspond to high geothermal gradient zones in all three areas. Moreover, the highest mercury values within the anomalies are found near the wells with the highest geothermal gradient. Such close correspondence between soil concentrations

424

Geological and Anthropogenic Factors Influencing Mercury Speciation in Mine  

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

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

425

Thief Process Removal of Mercury from Flue Gas  

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

Process for the Removal of Mercury from Flue Gas Process for the Removal of Mercury from Flue Gas Opportunity The Department of Energy's National Energy Technology Laboratory (NETL) is seeking licensing partners interested in implementing United States Patent Number 6,521,021 entitled "Thief Process for the Removal of Mercury from Flue Gas." Disclosed in this patent is a novel process in which partially combusted coal is removed from the combustion chamber of a power plant using a lance (called a "thief"). This partially combusted coal acts as a thermally activated adsorbent for mercury. When it is in- jected into the duct work of the power plant downstream from the exit port of the combustion chamber, mercury within the flue gas contacts and adsorbs onto the thermally activated sorbent. The sorbent-mercury

426

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

Open Energy Info (EERE)

Mercury Vapor At Lualualei Valley Area (Thomas, 1986) Mercury Vapor At Lualualei Valley Area (Thomas, 1986) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Lualualei Valley Area (Thomas, 1986) Exploration Activity Details Location Lualualei Valley Area Exploration Technique Mercury Vapor Activity Date Usefulness useful DOE-funding Unknown Notes Soil mercury and radon emanation surveys were performed over much of the accessible surface of Lualualei Valley (Cox and Thomas, 1979). The results of these surveys (Figs 7 and 8) delineated several areas in which soil mercury concentrations or radon emanation rates were substantially above normal background values. Some of these areas were apparently coincident with the mapped fracture systems associated with the caldera boundaries.

427

Oxidation of Mercury in Products of Coal Combustion  

SciTech Connect

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

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

2009-09-14T23:59:59.000Z

428

Evaluation of the mercury soil mapping geothermal exploration techniques  

Science Conference Proceedings (OSTI)

In order to evaluate the suitability of the soil mercury geochemical survey as a geothermal exploration technique, soil concentrations of mercury are compared to the distribution of measured geothermal gradients at Dixie Valley, Nevada; Roosevelt Hot Springs, Utah; and Noya, Japan. Zones containing high-mercury values are found to closely correspond to high geothermal gradient zones in all three areas. Moreover, the highest mercury values within the anomalies are found near the wells with the highest geothermal gradient. Such close correspondence between soil concentrations of mercury and high-measured geothermal gradients strongly suggests that relatively low-cost soil mercury geochemical sampling can be effective in identifying drilling targets within high-temperature areas.

Matlick, J.S.; Shiraki, M.

1981-10-01T23:59:59.000Z

429

Stabilization of Mercury in High pH Tank Sludges  

Science Conference Proceedings (OSTI)

DOE complex contains many tank sludges contaminated with mercury. The high pH of these tank sludges typically fails to stabilize the mercury, resulting in these radioactive wastes also being characteristically hazardous or mixed waste. The traditional treatment for soluble inorganic mercury species is precipitation as insoluble mercuric sulfide. Sulfide treatment and a commercial mercury-stabilizing product were tested on surrogate sludges at various alkaline pH values. Neither the sulfide nor the commercial product stabilized the mercury sufficiently at the high pH of the tank sludges to pass the Toxicity Characteristic Leach Procedure (TCLP) treatment standards of the Resource Conservation and Recovery Act (RCRA). The commercial product also failed to stabilize the mercury in samples of the actual tank sludges.

Spence, R.; Barton, J.

2003-02-24T23:59:59.000Z

430

NETL: Emissions Characterization - Direct Measurement of Mercury Reactions  

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

Direct Measurement of Mercury Reactions in Coal Power Plant Plumes: Pleasant Prairie Plant Direct Measurement of Mercury Reactions in Coal Power Plant Plumes: Pleasant Prairie Plant Under DOE-NETL Cooperative Agreement DE-FC26-03NT41724, EPRI, in collaboration with Frontier Geosciences and the University of North Dakota Energy and Environmental Research Center (EERC), will perform precise in-stack and in-plume sampling of mercury emitted from the stack of WE Energies' Pleasant Prairie coal-fired power plant near Kenosha, Wisconsin. The overall objective of the project is to clarify the role, rates and end result of chemical transformations that may occur to mercury that has been emitted from elevated stacks of coal-fired electric power plants. This information is critical in determining the role of coal-fired plants in mercury deposition and in developing cost-effective, environmentally sound policies and strategies for reducing the adverse environmental effects of mercury.

431

Mercury Speciation in Piscivorous Fish from Mining-impacted Reservoirs  

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

Mercury Speciation in Piscivorous Mercury Speciation in Piscivorous Fish from Mining-impacted Reservoirs Mercury toxicity generates environmental concerns in diverse aquatic systems because methylmercury enters the water column in diverse ways then biomagnifies through food webs. At the apex of many freshwater food webs, piscivorous fish can then extend that trophic transfer and potential for neurotoxicity to wildlife and humans. Mining activities, particularly those associated with the San Francisco Bay region, can generate both point and non-point mercury sources. Replicate XANES analyses on largemouth bass and hybrid striped bass from Guadalupe Reservoir (GUA), California and Lahontan Reservoir (LAH), Nevada, were performed to determine predominant chemical species of mercury accumulated by high-trophic-level piscivores that are exposed to elevated mercury in both solution and particulate phases in the water column.

432

Significance of Pre-Industrial and Older Anthropogenic Sources of Mercury in Ichawaynochaway Creek Watershed, Georgia  

Science Conference Proceedings (OSTI)

In response to concerns about elevated levels of mercury in fish tissue, the U.S. Environmental Protection Agency (EPA) has developed mercury Total Maximum Daily Loads (TMDL), which is a calculation of the maximum amount of mercury a waterbody can assimilate without exceeding the applicable water quality standard. These calculations assume that >99% of mercury load to the aquatic systems is derived from recent atmospheric deposition and that older anthropogenic mercury or mercury from terrestrial sources...

2004-06-16T23:59:59.000Z

433

Thief Carbon Catalyst for Oxidation of Mercury in Effluent Stream  

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

Carbon Catalyst for Oxidation of Mercury in Effluent Carbon Catalyst for Oxidation of Mercury in Effluent Stream Contact NETL Technology Transfer Group techtransfer@netl.doe.gov January 2012 Significance * Oxidizes heavy metal contaminants, especially mercury, in gas streams * Uses partially combusted coal ("Thief" carbon) * Yields an inexpensive catalyst * Cheap enough to be a disposable catalyst * Cuts long-term costs * Simultaneously addresses oxidation and adsorption issues Applications * Any process requiring removal of heavy

434

Development and Evaluation of Low Cost Mercury Sorbents  

Science Conference Proceedings (OSTI)

EPRI is conducting research to investigate sorbent injection for mercury removal in utility flue gas. This report describes laboratory work conducted from mid-1999 through mid-2000 to investigate the ability of low-cost sorbents to remove mercury from simulated and actual flue gas. The goal of this program is the development of effective mercury sorbents that can be produced at lower costs than existing commercial activated carbons. In this work, low-cost sorbents were prepared and then evaluated in labo...

2000-11-27T23:59:59.000Z

435

The Effect of Ammonia on Mercury Partitioning in Fly Ash  

Science Conference Proceedings (OSTI)

Management options and environmental assessments for fly ash are driven primarily by their physical and chemical characteristics. This report describes the results of a laboratory study on the leaching of mercury from several paired fly ash samples from facilities employing powdered activated carbon (PAC) injection for mercury control. While previous EPRI research has shown that mercury leaching from ash with PAC is negligible, it has also been found that ammonia complexes can increase the mobility of so...

2008-03-25T23:59:59.000Z

436

Controlling mercury spills in laboratories with a thermometer exchange program  

SciTech Connect

This paper presents a case for replacing mercury thermometers with their organic-liquid-filled counterparts. A review of liquid-in glass-thermometers is given. In addition, a brief summary of mercury's health effects and exposure limits is presented. Spill cleanup methods and some lessons learned from our experience are offered as well. Finally, an overview of the mercury thermometer exchange program developed at Lawrence Berkeley National Laboratory is presented.

McLouth, Lawrence D.

2002-03-25T23:59:59.000Z

437

State of Knowledge on Mercury Chemistry in Power Plant Plumes  

Science Conference Proceedings (OSTI)

Chemical transformations may occur in the flue gas plume of coal-fired power plants (CFPP) that convert reactive gaseous mercury (RGM) into gaseous elemental mercury (GEM). Since the chemical form of inorganic Hg determines its solubility in water and therefore its deposition rate, understanding this chemistry has important implications for emission control. This fact sheet summarizes the state-of-knowledge of mercury chemistry, kinetics, and thermodynamics in CFPP plumes.

2008-12-23T23:59:59.000Z

438

2009 Update on Mercury Capture by Wet Flue Gas Desulfurization  

Science Conference Proceedings (OSTI)

This technical update presents results of four research and development projects focused on understanding and enhancing mercury emissions control associated with wet flue gas desulfurization (FGD) technology. The first project was directed at characterizing partitioning of elemental and oxidized mercury species in solid, liquid, and gas phases within process streams involved in an operating commercial system. The second project explored dewatering options with an objective of producing low-mercury-conten...

2009-12-15T23:59:59.000Z

439

Development and Demonstration of Mercury Control by Dry Technologies  

Science Conference Proceedings (OSTI)

The Environmental Protection Agency (EPA) will regulate mercury emissions from coal-fired boilers under Title III of the Clean Air Act Amendments of 1990, with compliance slated for December 2007. It is thus very important for power producers to determine the amount of mercury emissions from their power plants, options for reducing mercury emissions, the cost-effectiveness of various removal technologies, and the potential impact on power plant operation and other air pollutant emissions.

2003-02-17T23:59:59.000Z

440

Thief carbon catalyst for oxidation of mercury in effluent stream  

DOE Patents (OSTI)

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

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

2011-12-06T23:59:59.000Z

Note: This page contains sample records for the topic "arsenic mercury radionuclides" 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

In Situ Iron Oxide Emplacement for Groundwater Arsenic Remediation  

E-Print Network (OSTI)

Iron oxide-bearing minerals have long been recognized as an effective reactive media for arsenic-contaminated groundwater remediation. This research aimed to develop a technique that could facilitate in situ oxidative precipitation of Fe3+ in a soil (sand) media for generating a subsurface iron oxide-based reactive barrier that could immobilize arsenic (As) and other dissolved metals in groundwater. A simple in situ arsenic treatment process was successfully developed for treating contaminated rural groundwater using iron oxide-coated sand (IOCS). Using imbibition flow, the system facilitated the dispersive transport of ferrous iron (Fe2+) and oxidant solutions in porous sand to generate an overlaying blanket where the Fe2+ was oxidized and precipitated onto the surface as ferric oxide. The iron oxide (FeOx) emplacement process was significantly affected by (1) the initial surface area and surface-bound iron content of the sand, (2) the pH and solubility of the coating reagents, (3) the stability of the oxidant solution, and (4) the chemical injection schedule. In contrast to conventional excavate-and-fill treatment technologies, this technique could be used to in situ replace a fresh iron oxide blanket on the sand and rejuvenate its treatment capacity for additional arsenic removal. Several bench-scale experiments revealed that the resultant IOCS could treat arsenic-laden groundwater for extended periods of time before approaching its effective life cycle. The adsorption capacity for As(III) and As(V) was influenced by (1) the amount of iron oxide accumulated on the sand surface, (2) the system pH, and (3) competition for adsorption sites from other groundwater constituents such as silicon (Si) and total dissolved solids (TDS). Although the IOCS could be replenished several times before exhaustion, the life cycle of the FeOx reactive barrier may be limited by the gradual loss of hydraulic conductivity induced by the imminent reduction of pore space over time.

Abia, Thomas Sunday

2011-12-01T23:59:59.000Z

442

Arsenic pilot plant operation and results : Anthony, New Mexico.  

Science Conference Proceedings (OSTI)

Sandia National Laboratories (SNL) is conducting pilot scale evaluations of the performance and cost of innovative water treatment technologies aimed at meeting the recently revised arsenic maximum contaminant level (MCL) for drinking water. The standard of 10 {micro}g/L (10 ppb) is effective as of January 2006. The pilot tests have been conducted in New Mexico where over 90 sites that exceed the new MCL have been identified by the New Mexico Environment Department. The pilot test described in this report was conducted in Anthony, New Mexico between August 2005 and December 2006 at Desert Sands Mutual Domestic Water Consumers Association (MDWCA) (Desert Sands) Well No.3. The pilot demonstrations are a part of the Arsenic Water Technology Partnership program, a partnership between the American Water Works Association Research Foundation (AwwaRF), SNL and WERC (A Consortium for Environmental Education and Technology Development). The Sandia National Laboratories pilot demonstration at the Desert Sands site obtained arsenic removal performance data for fourteen different adsorptive media under intermittent flow conditions. Well water at Desert Sands has approximately 20 ppb arsenic in the unoxidized (arsenite-As(III)) redox state with moderately high total dissolved solids (TDS), mainly due to high sulfate, chloride, and varying concentrations of iron. The water is slightly alkaline with a pH near 8. The study provides estimates of the capacity (bed volumes until breakthrough at 10 ppb arsenic) of adsorptive media in the same chlorinated water. Adsorptive media were compared side-by-side in ambient pH water with intermittent flow operation. This pilot is broken down into four phases, which occurred sequentially, however the phases overlapped in most cases.

Aragon, Malynda Jo; Everett, Randy L.; Siegel, Malcolm Dean; Aragon, Alicia R.; Kottenstette, Richard Joseph; Holub, William E., Jr.; Wright, Jerome L.; Dwyer, Brian P.

2007-09-01T23:59:59.000Z

443

Techniques for assessing the performance of in situ bioreduction and immobilization of metals and radionuclides in contaminated subsurface environments  

E-Print Network (OSTI)

Immobilization of Metals and Radionuclides in Contaminatedsubsurface metals and radionuclides. Research within DOEstoxic metals and radionuclides (e.g. Cr, U, Tc, Co) into a

2004-01-01T23:59:59.000Z

444

Selected radionuclides important to low-level radioactive waste management  

Science Conference Proceedings (OSTI)

The purpose of this document is to provide information to state representatives and developers of low level radioactive waste (LLW) management facilities about the radiological, chemical, and physical characteristics of selected radionuclides and their behavior in the environment. Extensive surveys of available literature provided information for this report. Certain radionuclides may contribute significantly to the dose estimated during a radiological performance assessment analysis of an LLW disposal facility. Among these are the radionuclides listed in Title 10 of the Code of Federal Regulations Part 61.55, Tables 1 and 2 (including alpha emitting transuranics with half-lives greater than 5 years). This report discusses these radionuclides and other radionuclides that may be significant during a radiological performance assessment analysis of an LLW disposal facility. This report not only includes essential information on each radionuclide, but also incorporates waste and disposal information on the radionuclide, and behavior of the radionuclide in the environment and in the human body. Radionuclides addressed in this document include technetium-99, carbon-14, iodine-129, tritium, cesium-137, strontium-90, nickel-59, plutonium-241, nickel-63, niobium-94, cobalt-60, curium -42, americium-241, uranium-238, and neptunium-237.

NONE

1996-11-01T23:59:59.000Z

445

Transuranic radionuclides dispersed into the aquatic environment, a bibliography  

Science Conference Proceedings (OSTI)

The purpose of this project was to compile a bibliography of references containing environmental transuranic radionuclide data. Our intent was to identify those parameters affecting transuranic radionuclide transport that may be generic and those that may be dependent on chemical form and/or environmental conditions (i.e., site specific) in terrestrial, aquatic and atmospheric environments An understanding of the unique characteristics and similarities between source terms and environmental conditions relative to transuranic radionuclide transport and cycling will provide the ability to assess and predict the long term impact on man and the environment. An additional goal of our literature review, was to extract the ranges of environmental transuranic radionuclide data from the identified references for inclusion in a data base. Related to source term, these ranges of data can be used to calculate the dose to man from the radionuclides, and to perform uncertainty analyses on these dose assessments. On the basis of our reviews, we have arbitrarily outlined five general source terms. These are fallout, fuel cycle waste, accidents, disposal sites and resuspension. Resuspension of the transuranic radionuclides is a unique source term, in that the radionuclides can originate from any of the other source terms. If these transuranic radionuclides become resuspended into the air, they then become important as a source of inhaled radionuclides.

Noshkin, V.E.; Stoker, A.C.; Wong, Kai M. [and others

1994-04-01T23:59:59.000Z

446

Airborne remote sensing of estuarine intertidal radionuclide concentrations.  

E-Print Network (OSTI)

??The ability to map industrial discharges through remote sensing provides a powerful tool in environmental monitoring. Radionuclide effluents have been discharged, under authorization, into the (more)

Rainey, Michael Patrick

1999-01-01T23:59:59.000Z

447

NETL: IEP - Mercury Emissions Control: Methods Development  

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

Methods Development Methods Development EPRI and NETL collaboratively funded a $3-million program under the DOE/ University of North Dakota Energy and Environmental Research Center (UNDEERC) Jointly Sponsored Research Program (JSRP) to evaluate, develop, and validate a mercury speciation method for coal-fired produced flue gas. There was a 60/40 percent split of the funding, as required under the JSRP for this two-year effort. The work conducted by the EERC identified the Ontario Hydro Method as the best mercury speciation method. The EERC has validated the Ontario Hydro Method at both pilot- and full-scale levels. Radian International aided in the full-scale validation, with a written protocol of the method being finalized through the American Society for Testing and Materials (ASTM).

448

Mercury Geochemical, Groundwater Geochemical, And Radiometric Geophysical  

Open Energy Info (EERE)

Geochemical, Groundwater Geochemical, And Radiometric Geophysical Geochemical, Groundwater Geochemical, And Radiometric Geophysical Signatures At Three Geothermal P