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


1

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

2

Integrated coke, asphalt and jet fuel production process and apparatus  

DOE Patents (OSTI)

A process and apparatus for the production of coke, asphalt and jet fuel from a feed of fossil fuels containing volatile carbon compounds therein is disclosed. The process includes the steps of pyrolyzing the feed in an entrained bed pyrolyzing means, separating the volatile pyrolysis products from the solid pyrolysis products, removing at least some coke from the solid pyrolysis products, fractionating the volatile pyrolysis products to produce an overhead stream and a bottom stream which is useful as asphalt for road pavement, condensing the overhead stream to produce a condensed liquid fraction and a noncondensable, gaseous fraction, and removing water from the condensed liquid fraction to produce a jet fuel-containing product. The disclosed apparatus is useful for practicing the foregoing process. The process provides a useful method of mass producing these products from materials such as coal, oil shale and tar sands. 1 fig.

Shang, Jer Yu.

1989-10-17T23:59:59.000Z

3

Integrated coke, asphalt and jet fuel production process and apparatus  

DOE Patents (OSTI)

A process and apparatus for the production of coke, asphalt and jet fuel m a feed of fossil fuels containing volatile carbon compounds therein is disclosed. The process includes the steps of pyrolyzing the feed in an entrained bed pyrolyzing means, separating the volatile pyrolysis products from the solid pyrolysis products removing at least one coke from the solid pyrolysis products, fractionating the volatile pyrolysis products to produce an overhead stream and a bottom stream which is useful as asphalt for road pavement, condensing the overhead stream to produce a condensed liquid fraction and a noncondensable, gaseous fraction, and removing water from the condensed liquid fraction to produce a jet fuel-containing product. The disclosed apparatus is useful for practicing the foregoing process. the process provides a useful method of mass producing and jet fuels from materials such as coal, oil shale and tar sands.

Shang, Jer Y. (McLean, VA)

1991-01-01T23:59:59.000Z

4

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

5

Process for removing heavy metal compounds from heavy crude oil  

DOE Patents (OSTI)

A process is provided for removing heavy metal compounds from heavy crude oil by mixing the heavy crude oil with tar sand; preheating the mixture to a temperature of about 650.degree. F.; heating said mixture to up to 800.degree. F.; and separating tar sand from the light oils formed during said heating. The heavy metals removed from the heavy oils can be recovered from the spent sand for other uses.

Cha, Chang Y. (Golden, CO); Boysen, John E. (Laramie, WY); Branthaver, Jan F. (Laramie, WY)

1991-01-01T23:59:59.000Z

6

Process for removal of sulfur compounds from fuel gases  

DOE Patents (OSTI)

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

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

1978-01-01T23:59:59.000Z

7

Process for removing an organic compound from water  

DOE Patents (OSTI)

A process for removing organic compounds from water is disclosed. The process involves gas stripping followed by membrane separation treatment of the stripping gas. The stripping step can be carried out using one or multiple gas strippers and using air or any other gas as stripping gas. The membrane separation step can be carried out using a single-stage membrane unit or a multistage unit. Apparatus for carrying out the process is also disclosed. The process is particularly suited for treatment of contaminated groundwater or industrial wastewater.

Baker, Richard W. (Palo Alto, CA); Kaschemekat, Jurgen (Palo Alto, CA); Wijmans, Johannes G. (Menlo Park, CA); Kamaruddin, Henky D. (San Francisco, CA)

1993-12-28T23:59:59.000Z

8

Tertiary nitrogen heterocyclic material to reduce moisture-induced damage in asphalt-aggregate mixtures  

DOE Patents (OSTI)

Asphalt-aggregate roads crack when subjected to freezing and thawing cycles. Herein, the useful life of asphalts are substantially improved by a minor amount of a moisture damage inhibiting agent selected from compounds having a pyridine moiety, including acid salts of such compounds. A shale oil fraction may serve as the source of the improving agent and may simply be blended with conventional petroleum asphalts.

Plancher, Henry (Laramie, WY); Petersen, Joseph C. (Laramie, WY)

1982-01-01T23:59:59.000Z

9

Method for removing chlorine compounds from hydrocarbon mixtures  

DOE Patents (OSTI)

A process for removing halide ions from a hydrocarbon feedstream containing halogenated hydrocarbons wherein the contaminated feedstock is contacted with a solution of a suitable oxidizing acid containing a lanthanide oxide, the acid being present in a concentration of at least about 50 weight percent for a time sufficient to remove substantially all of the halide ion from the hydrocarbon feedstock.

Janoski, Edward J. (Havertown, PA); Hollstein, Elmer J. (Wilmington, DE)

1985-12-31T23:59:59.000Z

10

Method for removing chlorine compounds from hydrocarbon mixtures  

DOE Patents (OSTI)

A process for removing halide ions from a hydrocarbon feedstream containing halogenated hydrocarbons wherein the contaminated feedstock is contacted with a solution of a suitable oxidizing acid containing a lanthanide oxide, the acid being present in a concentration of at least about 50 weight percent for a time sufficient to remove substantially all of the halide ion from the hydrocarbon feedstock.

Janoski, E.J.; Hollstein, E.J.

1984-09-29T23:59:59.000Z

11

Removal of sulfur compounds from combustion product exhaust  

DOE Patents (OSTI)

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

Cheng, Dah Y. (Palo Alto, CA)

1982-01-01T23:59:59.000Z

12

Removal of basic nitrogen compounds from hydrocarbon liquids  

DOE Patents (OSTI)

A method is provided for reducing the concentration of basic nitrogen compounds in hydrocarbonaceous feedstock fluids used in the refining industry by providing a solid particulate carbonaceous adsorbent/fuel material such as coal having active basic nitrogen complexing sites on the surface thereof and the coal with a hydrocarbonaceous feedstock containing basic nitrogen compounds to facilitate attraction of the basic nitrogen compounds to the complexing sites and the formation of complexes thereof on the surface of the coal. The adsorbent coal material and the complexes formed thereon are from the feedstock fluid to provide a hydrocarbonaceous fluid of reduced basic nitrogen compound concentration. The coal can then be used as fuel for boilers and the like.

Givens, Edwin N. (Bethlehem, PA); Hoover, David S. (New Tripoli, PA)

1985-01-01T23:59:59.000Z

13

Removal of arsenic compounds from spent catecholated polymer  

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

14

Hydraulic properties of asphalt concrete.  

E-Print Network (OSTI)

??This research has applied standard unsaturated flow models and laboratory methods common to soil analysis, to characterize the hydraulic properties of asphalt concrete. Wetting and… (more)

Pease, Ronald Eric

2010-01-01T23:59:59.000Z

15

Precipitate hydrolysis process for the removal of organic compounds from nuclear waste slurries  

DOE Patents (OSTI)

A process for removing organic compounds from a nuclear waste slurry comprising reacting a mixture of radioactive waste precipitate slurry and an acid in the presence of a catalytically effective amount of a copper(II) catalyst whereby the organic compounds in the precipitate slurry are hydrolyzed to form volatile organic compounds which are separated from the reacting mixture. The resulting waste slurry, containing less than 10 percent of the original organic compounds, is subsequently blended with high level radioactive sludge land transferred to a vitrification facility for processing into borosilicate glass for long-term storage. 2 figs., 3 tabs.

Doherty, J.P.; Marek, J.C.

1987-02-25T23:59:59.000Z

16

Bibliography of work on the photocatalytic removal of hazardous compounds from water and air  

DOE Green Energy (OSTI)

This is a bibliography of information in the open literature on work that has been done to date on the photocatalytic oxidation of compounds, principally organic compounds. The goal of the listing is removing hazardous oompounds from water or air. It contains lists of substances and literature citations. The bibliography includes information obtained through the middle of 1993 and some selected references for the balance of that year.

Blake, D.M.

1994-05-01T23:59:59.000Z

17

Composites for removing metals and volatile organic compounds and method thereof  

DOE Patents (OSTI)

Functionalized hydrophobic aerogel/solid support structure composites have been developed to remove metals and organic compounds from aqueous and vapor media. The targeted metals and organics are removed by passing the aqueous or vapor phase through the composite which can be in molded, granular, or powder form. The composites adsorb the metals and the organics leaving a purified aqueous or vapor stream. The species-specific adsorption occurs through specific functionalization of the aerogels tailored towards specific metals and/or organics. After adsorption, the composites can be disposed of or the targeted metals and/or organics can be reclaimed or removed and the composites recycled.

Coronado, Paul R. (Livermore, CA); Coleman, Sabre J. (Oakland, CA); Reynolds, John G. (San Ramon, CA)

2006-12-12T23:59:59.000Z

18

Asphalt Roofing Shingles Into Energy Project Summary Report  

DOE Green Energy (OSTI)

Based on a widely cited September, 1999 report by the Vermont Agency of Natural Resources, nearly 11 million tons of asphalt roofing shingle wastes are produced in the United States each year. Recent data suggests that the total is made up of about 9.4 million tons from roofing tear-offs and about 1.6 million tons from manufacturing scrap. Developing beneficial uses for these materials would conserve natural resources, promote protection of the environment and strengthen the economy. This project explored the feasibility of using chipped asphalt shingle materials in cement manufacturing kilns and circulating fluidized bed (CFB) boilers. A method of enhancing the value of chipped shingle materials for use as fuel by removing certain fractions for use as substitute raw materials for the manufacture of new shingles was also explored. Procedures were developed to prevent asbestos containing materials from being processed at the chipping facilities, and the frequency of the occurrence of asbestos in residential roofing tear-off materials was evaluated. The economic feasibility of each potential use was evaluated based on experience gained during the project and on a review of the well established use of shingle materials in hot mix asphalt. This project demonstrated that chipped asphalt shingle materials can be suitable for use as fuel in circulating fluidized boilers and cement kilns. More experience would be necessary to determine the full benefits that could be derived and to discover long term effects, but no technical barriers to full scale commercial use of chipped asphalt shingle materials in these applications were discovered. While the technical feasibility of various options was demonstrated, only the use of asphalt shingle materials in hot mix asphalt applications is currently viable economically.

Jameson, Rex, PE

2008-04-28T23:59:59.000Z

19

Process for removing halogenated aliphatic and aromatic compounds from petroleum products  

DOE Patents (OSTI)

A process for removing halogenated aliphatic and aromatic compounds, e.g., polychlorinated biphenyls, from petroleum products by solvent extraction. The halogenated aliphatic and aromatic compounds are extracted from a petroleum product into a polar solvent by contacting the petroleum product with the polar solvent. The polar solvent is characterized by a high solubility for the extracted halogenated aliphatic and aromatic compounds, a low solubility for the petroleum product and considerable solvent power for polyhydroxy compound. The preferred polar solvent is dimethylformamide. A miscible compound, such as, water or a polyhydroxy compound, is added to the polar extraction solvent to increase the polarity of the polar extraction solvent. The halogenated aliphatic and aromatic compounds are extracted from the highly-polarized mixture of water or polyhydroxy compound and polar extraction solvent into a low polar or nonpolar solvent by contacting the water or polyhydroxy compound-polar solvent mixture with the low polar or nonpolar solvent. The halogenated aliphatic and aromatic compounds and the low polar or nonpolar solvent are separated by physical means, e.g., vacuum evaporation. The polar and nonpolar solvents are recovered from recycling. The process can easily be designed for continuous operation. Advantages of the process include that the polar solvent and a major portion of the nonpolar solvent can be recycled, the petroleum products are reclaimable and the cost for disposing of waste containing polychlorinated biphenyls is significantly reduced.

Googin, John M. (Oak Ridge, TN); Napier, John M. (Oak Ridge, TN); Travaglini, Michael A. (Oliver Springs, TN)

1983-01-01T23:59:59.000Z

20

Process for removing halogenated aliphatic and aromatic compounds from petroleum products  

DOE Patents (OSTI)

A process is described for removing halogenated aliphatic and aromatic compounds, e.g., polychlorinated biphenyls, from petroleum products by solvent extraction. The halogenated aliphatic and aromatic compounds are extracted from a petroleum product into a polar solvent by contacting the petroleum product with the polar solvent. The polar solvent is characterized by a high solubility for the extracted halogenated aliphatic and aromatic compounds, a low solubility for the petroleum product and considerable solvent power for polyhydroxy compound. The preferred polar solvent is dimethylformamide. A miscible compound, such as, water or a polyhydroxy compound, is added to the polar extraction solvent to increase the polarity of the polar extraction solvent. The halogenated aliphatic and aromatic compounds are extracted from the highly-polarized mixture of water or polyhydroxy compound and polar extraction solvent into a low polar or nonpolar solvent by contacting the water or polyhydroxy compound-polar solvent mixture with the low polar or nonpolar solvent. The halogenated aliphatic and aromatic compounds and the low polar or nonpolar solvent are separated by physical means, e.g., vacuum evaporation. The polar and nonpolar solvents are recovered from recycling. The process can easily be designed for continuous operation. Advantages of the process include that the polar solvent and a major portion of the nonpolar solvent can be recycled, the petroleum products are reclaimable and the cost for disposing of waste containing polychlorinated biphenyls is significantly reduced. 1 fig.

Googin, J.M.; Napier, J.M.; Travaglini, M.A.

1983-09-20T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Literature Review: Asphalt Batching of MGP Tar-Containing Soil  

Science Conference Proceedings (OSTI)

As part of its manufactured gas plant (MGP) sites research effort, the Electric Power Research Institute (EPRI) is committed to developing and applying scientific and technological information to address the issues of remediation, treatment, and recycling of soils containing MGP tar and related organic compounds. This report deals with the issue of using MGP tar-containing soils in the manufacture of asphalt products.

1998-01-27T23:59:59.000Z

22

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

SciTech Connect

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

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

2008-07-02T23:59:59.000Z

23

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

E-Print Network (OSTI)

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

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

2008-01-01T23:59:59.000Z

24

Asphalt Oxidation Kinetics and Pavement Oxidation Modeling  

E-Print Network (OSTI)

Most paved roads in the United States are surfaced with asphalt. These asphalt pavements suffer from fatigue cracking and thermal cracking, aggravated by the oxidation and hardening of asphalt. This negative impact of asphalt oxidation on pavement performance has not been considered adequately in pavement design. Part of the reason is that the process of asphalt oxidation in pavement is not well understood. This work focused on understanding the asphalt oxidation kinetics and on developing pavement oxidation model that predicts asphalt oxidation and hardening in pavement under environmental conditions. A number of asphalts were studied in laboratory condition. Based on kinetics data, a fast-rate ? constant-rate asphalt oxidation kinetics model was developed to describe the early nonlinear fast-rate aging period and the later constant-rate period of asphalt oxidation. Furthermore, reaction kinetics parameters for the fast-rate and constant-rate reactions were empirically correlated, leading to a simplified model. And the experimental effort and time to obtain these kinetics parameters were significantly reduced. Furthermore, to investigate the mechanism of asphalt oxidation, two antioxidants were studied on their effectiveness. Asphalt oxidation was not significantly affected. It was found that evaluation of antioxidant effectiveness based on viscosity only is not reliable. The asphalt oxidation kinetics model was incorporated into the pavement oxidation model that predicts asphalt oxidation in pavement. The pavement oxidation model mimics the oxidation process of asphalt in real mixture at pavement temperatures. A new parameter, diffusion depth, defined the oxygen diffusion region in the mastic. A field calibration factor accounted for the factors not considered in the model such as the effect of small aggregate particles on oxygen diffusion. Carbonyl area and viscosity of binders recovered from field cores of three pavements in Texas were measured and were used for model calibration and validation. Results demonstrated that the proposed model estimates carbonyl growth over time in pavement, layer-by-layer, quite well. Finally, this work can be useful for incorporating asphalt oxidation into a pavement design method that can predict pavement performance with time and for making strategic decisions such as optimal time for maintenance treatments.

Jin, Xin

2012-05-01T23:59:59.000Z

25

Concrete & Asphalt Recycling into Reusable Products  

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

SNLNM Pollution Prevention Concrete & Asphalt Recycling into Reusable Products (SNLNM Pollution Prevention Program) March 18, 2010 Doug Vetter, PE, LEED-AP Sandia is a...

26

Variability of hot mix asphalt produced with reclaimed asphalt pavement  

E-Print Network (OSTI)

Pavement recycling operations have been used in the United States from the early 1900s to date. These recycling operations have been used for a variety of reasons including solid waste disposal problems, reduction of initial cost, and conservation of natural resources (aggregate, binder and energy). Adequate techniques to assess the variability of Reclaimed Asphalt Pavement (RAP) are lacking. The objectives of this research are to determine the variabilities of RAP and Hot Mix Asphalt (HMA), determine the influence of the RAP variability on the HMA variability, and compare the variability of virgin aggregates at the quarries and the aggregates that have been handled and transported to asphalt plant stockpiles. This thesis describes the compositional data analysis including the ternary diagrams for mixes and aggregates, a multivariate beta model, variability analysis using a multivariate variance assumption, and ternary quality control charts. It also describes the hypothesis tests using a k-variate student t distribution and an F-test. The following conclusions are obtained: i) RAP is better used in producing a mix with a relatively small top size 3/8" (Type S-III mix) or 1/2'' (Type S-I mix), and not with a sieve size larger than 1" (Type S-II mix); ii) RAP percent does not significantly influence the mix variability; it is desirable to use a large percentage of RAP in the Type S-I mix, i.e., more than 40% RAP; iii) On the average, the aggregate variability increases after transportation and stockpiling process; iv) On the average, the aggregate in the quarry has less variability than the same aggregate in the asphalt plant stockpile, therefore, aggregates in quarries are better controlled than aggregates in stockpiles; v) Variabilities of aggregates in quarries are slightly larger than the variability of RAP which is slightly larger than variabilities of Type S-II and S-III mixes. Type S-II and S-III mixes have the same variability and are slightly larger than the variability of the Type S-I mix; vi) The ternary diagram and the hypothesis test can be used to judge whether a contractor did a good job; vii) Ternary quality control chart shows the dynamic trend of a mix or an aggregate during the production period.

Yang, Guiqin

1999-01-01T23:59:59.000Z

27

Process for removing halogenated aliphatic and aromatic compounds from petroleum products. [Polychlorinated biphenyls; methylene chloride; perchloroethylene; trichlorofluoroethane; trichloroethylene; chlorobenzene  

DOE Patents (OSTI)

A process for removing halogenated aliphatic and aromatic compounds, e.g., polychlorinated biphenyls, from petroleum products by solvent extraction. The halogenated aliphatic and aromatic compounds are extracted from a petroleum product into a polar solvent by contracting the petroleum product with the polar solvent. The polar solvent is characterized by a high solubility for the extracted halogenated aliphatic and aromatic compounds, a low solubility for the petroleum product and considerable solvent power for polyhydroxy compound. The preferred polar solvent is dimethylformamide. A miscible polyhydroxy compound, such as, water, is added to the polar extraction solvent to increase the polarity of the polar extraction solvent. The halogenated aliphatic and aromatic compounds are extracted from the highly-polarized mixture of polyhydroxy compound and polar extraction solvent into a low polar or nonpolar solvent by contacting the polyhydroxy compound-polar solvent mixture with the low polar or nonpolar solvent. The halogenated aliphatic and aromatic compounds in the low polar or nonpolar solvent by physical means, e.g., vacuum evaporation. The polar and nonpolar solvents are recovered for recycling. The process can easily be designed for continuous operation. Advantages of the process include that the polar solvent and a major portion of the nonpolar solvent can be recycled, the petroleum products are reclaimable and the cost for disposing of waste containing polychlorinated biphenyls is significantly reduced. 2 tables.

Googin, J.M.; Napier, J.M.; Travaglini, M.A.

1982-03-31T23:59:59.000Z

28

Method and apparatus for converting and removing organosulfur and other oxidizable compounds from distillate fuels, and compositions obtained thereby  

DOE Patents (OSTI)

The present disclosure is directed to a multi-stage system and a process utilizing said system with the design of reducing the sulfur-content in a liquid comprising hydrocarbons and organosulfur compounds. The process comprising at least one of the following states: (1) an oxidation stage; (2) an extraction state; (3) a raffinate washing stage; (4) a raffinate polishing stage; (5) a solvent recovery stage; (6) a solvent purification stage; and (7) a hydrocarbon recovery stage. The process for removing sulfur-containing hydrocarbons from gas oil, which comprises oxidizing gas oil comprising hydrocarbons and organosulfur compounds to obtain a product gas oil.

D' Alessandro, Robert N. (Spanish Fort, AL); Tarabocchia, John (Parsippany, NJ); Jones, Jerald Andrew (Frankfurt am Main, DE); Bonde, Steven E. (West Richard, WA); Leininger, Stefan (Langenselbold, DE)

2010-10-26T23:59:59.000Z

29

Characterization of asphalt additive produced from hydroretorted Alabama shale  

SciTech Connect

Shale oil, produced from beneficiated Alabama shale by pressurized fluidized-bed hydroretorting, was fractionated to produce shale oil asphalt additives (SOA). Three shale oil fractions boiling above 305{degrees}C were added to standard AC-20 asphalt to improve pavement properties. The physical properties and aging characteristics of AC-20 asphalt binder (cement) containing SOA are similar to those of unmodified AC-20 asphalt binder. Asphalt pavement briquettes made with AC-20 asphalt binder containing 5 to 10 percent SOA have superior resistance to freeze-thaw cracking and a greater retention of tensile strength when wet compared to pavement briquettes containing AC-20 binder alone.

Rue, D.M.; Roberts, M.J.

1992-12-31T23:59:59.000Z

30

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

E-Print Network (OSTI)

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

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

2008-01-01T23:59:59.000Z

31

Annual Idaho Asphalt Conference October 27 28, 2010  

E-Print Network (OSTI)

50th Annual Idaho Asphalt Conference October 27 ­ 28, 2010 Moscow, ID Taj Anderson Poe Asphalt@cityofnampa.us Fouad Bayomy University of Idaho Moscow, ID Shane Beck Asphalt Zipper Inc. 831 East 340 South Suite 100 American Fork, UT 84003 Phone: 8018473200 laurat@asphaltzipper.com Lee Bernardi Idaho

Kyte, Michael

32

What's the future for rubberized asphalt  

SciTech Connect

This article describes the debate over the use of rubberized asphalt for highway surfacing. The Department of Transportation claims that the process is too costly; that it presents potential air pollution, safety and health problems. They also claim that there is a lack of understanding between rubber and asphalt cement and of the recyclability of the product. The Legislative Commission on Solid Waste Management claims that the mixture performs as well or better than conventional asphalt at reduced thicknesses. In addition, there could be savings of local funds currently expended for regulation of tire dumps, fire-fighting and clean-up, vector control and scrap tire disposal costs ranging from $.50 to $2.00 per tire.

Not Available

1991-04-01T23:59:59.000Z

33

Removal of arsenic, vanadium, and/or nickel compounds from petroliferous liquids  

DOE Patents (OSTI)

Described is a process for removing arsenic, vanadium, and/or nickel from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. For vanadium and nickel removal an amine, preferably a diamine is included. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic, vanadium, and/or nickel bound to it from contacting petroliferous liquid as described above and involves: treating the spent polymer containing any vanadium and/or nickel with an aqueous acid to achieve an acid pH; and, separating the solids from the liquid; and then 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, separating the solids and liquids from each other. Preferably the regeneration treatment of arsenic containing catecholated polymer is in two steps wherein the first step is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, the steps are repeated using a bicarbonate.

Fish, Richard H. (Berkeley, CA)

1986-01-01T23:59:59.000Z

34

Removal of arsenic, vanadium and/or nickel compounds from spent catecholated polymer  

DOE Patents (OSTI)

Described is a process for removing arsenic, vanadium, and/or nickel from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. For vanadium and nickel removal an amine, preferably a diamine is included. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic, vanadium, and/or nickel bound to it from contacting petroliferous liquid as described above and involves: treating the spent polymer containing any vanadium and/or nickel with an aqueous acid to achieve an acid pH; and, separating the solids from the liquid; and then 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, separating the solids and liquids from each other. Preferably the regeneration treatment of arsenic containing catecholated polymer is in two steps wherein the first step is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, the steps are repeated using a bicarbonate.

Fish, Richard H. (Berkeley, CA)

1987-01-01T23:59:59.000Z

35

Removal of arsenic, vanadium and/or nickel compounds from spent catecholated polymer  

DOE Patents (OSTI)

Described is a process for removing arsenic, vanadium, and/or nickel from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. For vanadium and nickel removal an amine, preferably a diamine is included. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic, vanadium, and/or nickel bound to it from contacting petroliferous liquid as described above and involves: treating the spent polymer containing any vanadium and/or nickel with an aqueous acid to achieve an acid pH; and, separating the solids from the liquid; and then treating said spent catecholated polystyrene, at a temperature in the range of about 20 to 100 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, separating the solids and liquids from each other. Preferably the regeneration treatment of arsenic containing catecholated polymer is in two steps wherein the first step is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, the steps are repeated using a bicarbonate.

Fish, R.H.

1987-04-21T23:59:59.000Z

36

Removal of arsenic, vanadium, and/or nickel compounds from petroliferous liquids  

DOE Patents (OSTI)

Described is a process for removing arsenic, vanadium, and/or nickel from petroliferous derived liquids (shale oil, SRC, etc.) by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. For vanadium and nickel removal an amine, preferably a diamine is included. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic, vanadium, and/or nickel bound to it from contacting petroliferous liquid as described above and involves: treating the spent polymer containing any vanadium and/or nickel with an aqueous acid to achieve an acid pH; and, separating the solids from the liquid; and then treating said spent catecholated polystyrene, at a temperature in the range of about 20/sup 0/ to 100/sup 0/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, separating the solids and liquids from each other. Preferably the regeneration treatment of arsenic containing catecholated polymer is in two steps wherein the first step is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, the steps are repeated using a bicarbonate.

Fish, R.H.

1985-05-17T23:59:59.000Z

37

Idaho Asphalt Conference Attendance List Andy Abrams  

E-Print Network (OSTI)

51st Idaho Asphalt Conference ­ Attendance List Andy Abrams STRATA, Inc. 1428 S. Main St. Moscow, Idaho 83843 208-882-1006 ajabrams@stratageotech.com John Arambarri Idaho Transportation Department - District 3 999 West Main St Boise, Idaho 83702 Paul Archibald Idaho Transportation Department PO Box 4700

Kyte, Michael

38

Hanford Permanent Isolation Barrier Program: Asphalt technology development  

SciTech Connect

An important component of the Hanford Permanent Isolation Barrier is the use of a two-layer composite asphalt system, which provides backup water diversion capabilities if the primary capillary barrier fails to meet infiltration goals. Because of asphalt`s potential to perform to specification over the 1000-year design life criterion, a composite asphalt barrier (HMAC/fluid-applied polymer-modified asphalt) is being considered as an alternative to the bentonite clay/high density poly(ethylene) barriers for the low-permeability component of the Hanford Permanent Isolation Barrier. The feasibility of using asphalt as a long-term barrier is currently being studied. Information that must be known is the ability of asphalt to retain desirable physical properties over a period of 1000 years. This paper presents the approach for performing accelerated aging tests and evaluating the performance of samples under accelerated conditions. The results of these tests will be compared with asphalt artifact analogs and the results of modeling the degradation of the selected asphalt composite to make life-cycle predictions.

Freeman, H.D.; Romine, R.A.

1994-11-01T23:59:59.000Z

39

An investigation of the use of tire rubber in asphalt  

E-Print Network (OSTI)

The use of asphalt-rubber has been mandated without the needed experience, design procedures, and construction guidelines. The purpose of this study is to determine optimal blend parameters that will enable maximum performance of the asphalt-rubber binder. The selected variables chosen are curing time, curing temperature, rubber content (weight percent), rubber particle size, base asphalt type, and carbonyl area. Results confirmed that the addition of rubber increased the viscosity of the asphalt binder at high temperatures, lowered the creep stiffness of the binder at low temperatures, and improved the overall temperature susceptibility. Increasing the rubber content in the asphalt was shown to further improve pavement performance. In addition, the use of smaller particles of rubber was found to decrease the creep stiffness at low temperatures (60QC). It was also determined that the type of asphalt and the type of rubber play important roles of meeting the criteria of an improved asphaltrubber binder. For example, the Murphy asphalt reblended with Sun recycling agent (AC-5) showed the least improvement to the addition of rubber compared with the Fina AC-10, Exxon AC-10, and Exxon AC-5. With respect to rubber type, the Rouse rubber was determined to improve Theological properties of the asphalt-rubber binder more than the Tire-Gator rubber. The curing process was also shown to increase the breakdown of the rubber into the asphalt. This phenomenon can be attributed to the devulcanization of the rubber in the mixer apparatus where extreme shear rates and temperatures were used.

Koo, Heamo Lee

1996-01-01T23:59:59.000Z

40

Particulate Matter Sampling and Volatile Organic Compound Removal for Characterization of Spark Ignited Direct Injection Engine Emissions  

Science Conference Proceedings (OSTI)

More stringent emissions regulations are continually being proposed to mitigate adverse human health and environmental impacts of internal combustion engines. With that in mind, it has been proposed that vehicular particulate matter (PM) emissions should be regulated based on particle number in addition to particle mass. One aspect of this project is to study different sample handling methods for number based aerosol measurements, specifically, two different methods for removing volatile organic compounds (VOCs). One method is a thermodenuder (TD) and the other is an evaporative chamber/diluter (EvCh). These sample handling methods have been implemented in an engine test cell with a spark ignited direct injection (SIDI) engine. The engine was designed for stoichiometric, homogeneous combustion. SIDI is of particular interest for improved fuel efficiency compared to other SI engines, however, the efficiency benefit comes with greater PM emissions and may therefore be subject to the proposed number based PM regulation. Another aspect of this project is to characterize PM from this engine in terms of particle number and composition.

Matthias, Nicholas; Farron, Carrie; Foster, David E.; Andrie, Michael; Krieger, Roger; Najt, Paul M.; Narayanaswamy, Kushal; Solomon, Arun S.; Zelenyuk, Alla

2012-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Study for Technology of Asphalt Pavement Aggregate Washed by Cycle Limewater  

Science Conference Proceedings (OSTI)

Technology of asphalt pavement aggregate washed by cycle limewater was put forward for the first time in this paper. Before and after the aggregate was washed by cycle limewater, aggregate mud content, aggregate asphalt adhesion and asphalt mixture water ... Keywords: energy conservation, emissions reduction, cycle limewater, wash, asphalt pavement aggregate

Jiang Tao; Sun Bin

2010-12-01T23:59:59.000Z

42

Recycled rubber, aggregate, and filler in asphalt paving mixtures. Transportation research record  

SciTech Connect

;Contents(Partial): Evaluation Systems for Crumb Rubber Modified Binders and Mixtures; Hot Mix Asphalt Rubber Applications in Virginia; Evaluation of Pyrolized Carbon Black from Scrap Tires as Additive in Hot Mix Asphalt; Use of Scrap Tire Chips in Asphaltic Membrane; Effects of Mineral Fillers on Properties of Stone Matrix Asphalt Mixtures; and Quantitative Analysis of Aggregate Based on Hough Transform.

NONE

1996-12-31T23:59:59.000Z

43

HP-GPC characterization of asphalt and modified asphalts from gulf countries and their relation to performance based properties  

Science Conference Proceedings (OSTI)

Asphalt producing refineries in the Gulf countries include Ras Tanura and Riyadh (Saudi Arabia), Al-Ahmadi (Kuwait), and BAPCO (Bahrain). Riyadh and Ras Tanura refineries are located in the central and eastern Saudi Arabia respectively. Arabian light crude oil is used to produce 2000 to 3000 tons of asphalt per day using vacuum distillation, air blowing and grade blending techniques to produce 60/70 penetration grade asphalts in each of these two Saudi refineries. All of the asphalt cement used in Saudi Arabia, Qatar and parts of the United Arab Emirates is supplied by Riyadh and Ras Tanura refineries. Al-Ahmadi refinery supplies all of the asphalt cement needed for construction in the state of Kuwait. Ratwi-Burgan crude off mix is used to produce 750 to 1000 tons of asphalt per day using vacuum distillation and air blowing processes. This study was initiated to evaluate different locally available polymers in order to identify potential polymers to modify asphalts to satisfy the performance requirements in the Gulf countries environmental conditions.

Wahhab, H.I.A.; Ali, M.F.; Asi, I.M.; Dubabe, I.A. [King Fahd Univ. of Petroleum and Minerals, Dhahran (Saudi Arabia)

1996-12-31T23:59:59.000Z

44

Excess Foundry Sand Characterization and Experimental Investigation in Controlled Low-Strength Material and Hot-Mixing Asphalt  

SciTech Connect

This report provides technical data regarding the reuse of excess foundry sand. The report addresses three topics: a statistically sound evaluation of the characterization of foundry sand, a laboratory investigation to qualify excess foundry sand as a major component in controlled low-strength material (CLSM), and the identification of the best methods for using foundry sand as a replacement for natural aggregates for construction purposes, specifically in asphalt paving materials. The survival analysis statistical technique was used to characterize foundry sand over a full spectrum of general chemical parameters, metallic elements, and organic compounds regarding bulk analysis and leachate characterization. Not limited to characterization and environmental impact, foundry sand was evaluated by factor analyses, which contributes to proper selection of factor and maximization of the reuse marketplace for foundry sand. Regarding the integration of foundry sand into CLSM, excavatable CLSM and structural CLSM containing different types of excess foundry sands were investigated through laboratory experiments. Foundry sand was approved to constitute a major component in CLSM. Regarding the integration of foundry sand into asphalt paving materials, the optimum asphalt content was determined for each mixture, as well as the bulk density, maximum density, asphalt absorption, and air voids at Nini, Ndes, and Nmax. It was found that foundry sands can be used as an aggregate in hot-mix asphalt production, but each sand should be evaluated individually. Foundry sands tend to lower the strength of mixtures and also may make them more susceptible to moisture damage. Finally, traditional anti-stripping additives may decrease the moisture sensitivity of a mixture containing foundry sand, but not to the level allowed by most highway agencies.

Paul J. Tikalsky, Hussain U. Bahia, An Deng and Thomas Snyder

2004-10-15T23:59:59.000Z

45

Excess Foundry Sand Characterization and Experimental Investigation in Controlled Low-Strength Material and Hot-Mixing Asphalt  

Science Conference Proceedings (OSTI)

This report provides technical data regarding the reuse of excess foundry sand. The report addresses three topics: (1) a statistically sound evaluation of the characterization of foundry sand, (2) a laboratory investigation to qualify excess foundry sand as a major component in controlled low-strength material (CLSM), and (3) the identification of the best methods for using foundry sand as a replacement for natural aggregates for construction purposes, specifically in asphalt paving materials. The survival analysis statistical technique was used to characterize foundry sand over a full spectrum of general chemical parameters, metallic elements, and organic compounds regarding bulk analysis and leachate characterization. Not limited to characterization and environmental impact, foundry sand was evaluated by factor analyses, which contributes to proper selection of factor and maximization of the reuse marketplace for foundry sand. Regarding the integration of foundry sand into CLSM, excavatable CLSM and structural CLSM containing different types of excess foundry sands were investigated through laboratory experiments. Foundry sand was approved to constitute a major component in CLSM. Regarding the integration of foundry sand into asphalt paving materials, the optimum asphalt content was determined for each mixture, as well as the bulk density, maximum density, asphalt absorption, and air voids at N{sub ini}, N{sub des}, and N{sub max}. It was found that foundry sands can be used as an aggregate in hot-mix asphalt production, but each sand should be evaluated individually. Foundry sands tend to lower the strength of mixtures and also may make them more susceptible to moisture damage. Finally, traditional anti-stripping additives may decrease the moisture sensitivity of a mixture containing foundry sand, but not to the level allowed by most highway agencies.

Pauul J. Tikalsky

2004-10-31T23:59:59.000Z

46

Relationship Between Surface Free Energy and Total Work of Fracture of Asphalt Binder and Asphalt Binder-Aggregate Interfaces  

E-Print Network (OSTI)

Performance of asphalt mixtures depends on the properties of its constituent materials, mixture volumetrics, and external factors such as load and environment. An important material property that influences the performance of an asphalt mixture is the surface free energy of the asphalt binder and the aggregate. Surface free energy, which is a thermodynamic material property, is directly related to the adhesive bond energy between the asphalt binder and the aggregate as well as the cohesive bond energy of the asphalt binder. This thermodynamic material property has been successfully used to select asphalt binders and aggregates that have the necessary compatibility to form strong bonds and resist fracture. Surface free energy, being based on thermodynamics, assumes the asphalt binder is a brittle elastic material. In reality, the asphalt binder is not brittle and dissipates energy during loading and unloading. The total work of fracture is the culmination of all energy inputted into the sample to create two new surfaces of unit area and is dependent on the test geometry and testing conditions (e.g., temperature, loading rate, specimen size, etc.). The magnitude of the bond energy (either adhesive or cohesive) can be much smaller in magnitude when compared to the total work of fracture measured using mechanical tests (i.e., peel test, pull-off test, etc.). Despite the large difference in magnitude, there exists evidence in the literature supporting the use of the bond energy to characterize the resistance of composite systems to cohesive and/or adhesive failures. If the bond energy is to be recognized as a useful screening tool by the paving industry, the relationship between the bond energy and total work of fracture needs to be understood and verified. The effect of different types of modifications (addition of polymers, addition of anti-strip agents, and aging) on the surface free energy components of various asphalt binders was explored in order to understand how changes in the surface free energy components are related to the performance of the asphalt mixtures. After the asphalt binder-aggregate combination was explored, the next step was to study how the surface free energy of water was affected by contact with the asphalt binder-aggregate interface. Aggregates, which have a pH of greater than seven, will cause the pH of water that contacts them to increase. A change in the pH of the contacting water could indicate a change in its overall surface free energy, which might subsequently increase or decrease the water's moisture damage potential. With surface free energy fully explored, the total work of fracture was measured using pull-off tests for asphalt binder-aggregate combinations with known surface free energy components. In order to fully explore the relationship between bond energy and total work of fracture, temperature, loading rate, specimen geometry, and moisture content were varied in the experiments. The results of this work found that modifications made to the asphalt binder can have significant positive or negative effects on its surface free energy components and bond energy. Moreover, the results from the pull-off tests demonstrated that a relationship exists between bond energy (from surface free energy) and total work of fracture (from pull-off tests), and that surface free energy can be used to estimate the performance of asphalt binder-aggregate combinations.

Howson, Jonathan Embrey

2011-08-01T23:59:59.000Z

47

Research on the microstructure and property of an anion rubber modified asphalt  

Science Conference Proceedings (OSTI)

The anion rubber modified asphalt (ARMA) mixture was first successfully developed with a unique process. In the development process, rubber and asphalt were mixed in the same proportion. Furthermore, the microstructure and modification mechanism of the ...

Wei Hong, Qingshan Li, Guoquan Guan, Youbo Di, Jing Sun, Tifeng Jiao, Guangzhong Xing

2013-01-01T23:59:59.000Z

48

Development of asphalts and pavements using recycled tire rubber. Phase 1: technical feasibility. Final report  

Science Conference Proceedings (OSTI)

This report documents the technical progress made on the development of asphalts and pavements using recycled tire rubber.

Bullin, J.A.; Davison, R.R.; Glover, C.J. [and others

1998-01-01T23:59:59.000Z

49

Consultant’s Handbook Office of the University Architect Engineering Utilities and Construction 32 1216 – Asphalt Paving  

E-Print Network (OSTI)

Asphalt pavements on the main campus are to be surfaced with hot-mix asphalt concrete. Reference: The principle reference for materials and methods is the "Indiana Department of Transportation Standard Specifications, " latest edition (INDOT). Installation Methods: All installation and sub-grade preparation methods shall conform to the appropriate section of the INDOT Spec. Unsuitable sub-grade material shall be removed and replaced with compacted suitable material or covered with appropriate construction grade fabric prior to subbase installation. Tack coat will be used only when overlayment of existing asphalt concrete must be postponed longer than five months. Light Duty Pavement: Description: One and a quarter inch (1.25") of compacted top on top of two inches (2") of compacted binder on top of four inches (4") of compacted type #53 granular sub-base. Uses: Pedestrian walks with minimal vehicular traffic expected and no emergency vehicles planned. Medium Duty Pavement: Description: One and half inches (1.5") of compacted top surface on top of three inches (3") of compacted binder on top of eight inch (8") of compacted Type #53 granular sub-base. Uses: Pedestrian walks with moderate vehicular use expected or for use as planned emergency access. Parking areas with no mass transit vehicles using driving lanes. Service drives Roads without constant, heavy vehicular traffic.

unknown authors

2005-01-01T23:59:59.000Z

50

Hanford Permanent Isolation Barrier Program: Asphalt technology test plan  

SciTech Connect

The Hanford Permanent Isolation Barriers use engineered layers of natural materials to create an integrated structure with backup protective features. The objective of current designs is to develop a maintenance-free permanent barrier that isolates wastes for a minimum of 1000 years by limiting water drainage to near-zero amounts. Asphalt is being used as an impermeable water diversion layer to provide a redundant layer within the overall barrier design. Data on asphalt barrier properties in a buried environment are not available for the required 100-year time frame. The purpose of this test plan is to outline the activities planned to obtain data with which to estimate performance of the asphalt layers.

Freeman, H.D.; Romine, R.A.

1994-05-01T23:59:59.000Z

51

Use of recycled chunk rubber asphalt concrete (CRAC) on low volume roads and use of recycled crumb rubber modifier in asphalt pavements. Final report, June 1993-June 1995  

SciTech Connect

The major objective of this project was to formulate a Chunk Rubber Asphalt Concrete (CRAC) mix for use on low volume roads. CRAC is a rubber modified asphalt concrete product produced by the `dry process` where rubber chunks of 1/2 inch size are used as aggregate in a cold mix with a type C fly ash. The second objective of this project was to develop guidelines concerning the use of rubber modified asphalt concrete hot mix to include: (1) Design methods for use of asphalt-rubber mix for new construction and overlay, (2) Mix design method for asphalt-rubber, and (3) Test method for determining the amount of rubber in an asphalt-rubber concrete for quality control purposes.

Hossain, M.; Funk, L.P.; Sadeq, M.A.; Marucci, G.

1995-06-01T23:59:59.000Z

52

Bibliography of work on the heterogeneous photocatalytic removal of hazardous compounds from water and air, Update Number 2 to October 1996  

DOE Green Energy (OSTI)

The Solar Industrial Program has developed processes that destroy hazardous substances in or remove them from water and air. The processes of interest in this report are based on the application of heterogeneous photocatalysts, principally titanium dioxide or modifications thereof, but work on other heterogeneous catalysts is included in this compilation. This report continues bibliographies that were published in May, 1994, and October, 1995. The previous reports included 663 and 574 citations, respectively. This update contains an additional 518 references. These were published during the period from June 1995 to October 1996, or are references from prior years that were not included in the previous reports. The work generally focuses on removing hazardous contaminants from air or water to meet environmental or health regulations. This report also references work on properties of semiconductor photocatalysts and applications of photocatalytic chemistry in organic synthesis. This report follows the same organization as the previous publications. The first part provides citations for work done in a few broad categories that are generic to the process. Three tables provide references to work on specific substances. The first table lists organic compounds that are included in various lists of hazardous substances identified by the US Environmental Protection Agency (EPA). The second table lists compounds not included in those categories, but which have been treated in a photocatalytic process. The third table covers inorganic compounds that are on EPA lists of hazardous materials or that have been treated by a photocatalytic process. A short update on companies that are active in providing products or services based on photocatalytic processes is provided.

Blake, D.M.

1997-01-01T23:59:59.000Z

53

Evaluation of the filler effects on fatique cracking and permanent deformation of asphalt concrete mixtures  

E-Print Network (OSTI)

The addition of hydrated lime to asphalt has shown to be beneficial with an improvement in the Theological properties of the binder, as well as resistance to permanent deformation (rutting) and fatigue cracking of asphalt concrete mixtures. The addition of hydrated lime produces a filler effect where the result is a stiffening of the asphalt mixture, thus improving the resistance to permanent deformation. The fatigue characteristics of the asphalt mixtures did not worsen from this stiffening effect, but were either improved or similar. The Superpave Performance Grade was not significantly indicative of the filler effects induced by the hydrated lime. However, evaluation of the physical properties, G*/sin5 and G*sin5 were indicative of significant filler effects induced by the hydrated lime. Creep properties, stiffness and m-value showed no substantial change with the addition of lime. The use of 10 to 20% mass concentration of hydrated lime can effectively improve the rutting resistance of the unaged and aged binder with little practical effect on the low temperature and fatigue properties. The filler effects produced through the addition of hydrated lime to the asphalt yielded asphalt mixtures less susceptible to rutting. In most cases, the fatigue life of the asphalt mixtures improved as well. The reference modulus and creep compliance of the asphalt mixtures with lime had shown to have greater fatigue life. In most cases, Stone Matrix Asphalt (SMA) mixtures with lime showed greater resistance to rutting, as well as greater fatigue life. The filler effects from the hydrated lime, as well as the stone-on-stone contact and stiffening from the mastic (two characteristics of SMA mixtures) improved these properties. The addition of hydrated lime to asphalt improved the G*/sin5 and G*sin8 of the asphalt binders. The use of these asphalt binders in asphalt concrete mixtures increased the resistance to rutting and fatigue life. It is apparent that a correlation exists between the asphalt binder and mixture test results.

Izzo, Richard P

1997-01-01T23:59:59.000Z

54

Energy Efficient Removal of Volatile Organic Compounds (VOCs) and Organic Hazardous Air Pollutants (o-HAPs) from Industrial Waste Streams by Direct Electron Oxidation  

SciTech Connect

This research program investigated and quantified the capability of direct electron beam destruction of volatile organic compounds and organic hazardous air pollutants in model industrial waste streams and calculated the energy savings that would be realized by the widespread adoption of the technology over traditional pollution control methods. Specifically, this research determined the quantity of electron beam dose required to remove 19 of the most important non-halogenated air pollutants from waste streams and constructed a technical and economic model for the implementation of the technology in key industries including petroleum refining, organic & solvent chemical production, food & beverage production, and forest & paper products manufacturing. Energy savings of 75 - 90% and green house gas reductions of 66 - 95% were calculated for the target market segments.

Testoni, A. L.

2011-10-19T23:59:59.000Z

55

Idaho Asphalt Conference October 24, 25, 2012 Attendee List  

E-Print Network (OSTI)

52nd Idaho Asphalt Conference ­ October 24, 25, 2012 Attendee List Kimbol Allen Idaho Transportation Department 216 South Date Street Shoshone, ID 83352 208-886-7805 kimbol.allen@itd.idaho.gov John Arambarri Idaho Transportation Department P.O. Box 8028 Boise, ID 83707-2028 208-332-7161 john.arambarri@itd.idaho

Kyte, Michael

56

Downstream Processing of Recombinant Proteins from Transgenic Plant Systems: Phenolic Compounds Removal from Monoclonal Antibody Expressing Lemna minor and Purification of Recombinant Bovine Lysozyme from Sugarcane  

E-Print Network (OSTI)

Transgenic plant systems have been proposed as bioreactors in the production of pharmaceutical and industrial proteins. The economic benefits of inexpensive plant production systems could be erased if the downstream processing ends up being expensive. To avoid monoclonal antibody (mAb) modification or fouling of chromatography resins, removal of phenolics from plant extracts is desirable. Removal of major phenolics in Lemna extracts was evaluated by adsorption to PVPP, XAD-4, IRA-402 and Q-Sepharose resins. Analysis of phenolics adsorption to XAD-4, IRA-402 and Q-Sepharose showed superior dynamic binding capacities at pH 4.5 than at 7.5. The economic analysis using SuperPro Designer 7.0 indicated that addition of a phenolics adsorption step would increase mAb production cost only 20% by using IRA-402 compared to 35% for XAD-4 resin. The overall mAb processing cost can be reduced by implementing a phenolics removal step. To understand phenolics-resin interactions, adsorption isotherms of phenolic compounds (chlorogenic acid, ferulic acid, rutin, syringic acid and vitexin-2-O-rhamnoside) from different phenolic classes on three resins (IRA-402, PVPP, XAD-4) at pH 4.5 and 7.5 were determined. Differences in adsorption with the type of phenolics were observed, and PVPP was not efficient for phenolics removal. Screening of sugarcane lines for bovine lysozyme (BvLz) accumulation indicated that expression levels are still inadequate for commercial development. To maximize BvLz extraction, pH and ionic strength were evaluated; five conditions resulted in equivalent BvLz/TSP ratio. Membrane filtration process using BvLz extracts attained partial removal of native proteins by the 100 kDa membrane step, but also BvLz loss (21-29%). Regardless of the extraction condition, at least 47% of the starting BvLz was lost during the membrane processing. None of the evaluated extraction conditions caused a substantial recovery of BvLz in the concentrate. Alternative purification options for the IEX+HIC process, which achieved 95% BvLz purity, were tested. Direct loading of sugarcane extract concentrate on HIC and XAD-4 pretreatment of juice did not recovered BvLz as effectively as the IEX chromatography. Pure BvLz was obtained by the XAD+HIC process, but higher purification fold and HIC yield were achieved by the IEX+HIC process, due to the complete separation of BvLz and 18-kDa protein.

Barros, Georgia

2012-05-01T23:59:59.000Z

57

A novel technique for the production of cool colored concrete tile and asphalt shingle roofing products  

E-Print Network (OSTI)

Wavelength (nm) In press at Solar Energy Materials & Solarcool asphalt shingles. Solar Energy Materials & Solar Cellsof common colorants, Solar Energy Materials & Solar Cells

Levinson, Ronnen

2010-01-01T23:59:59.000Z

58

Use of VFDs on Asphalt Plant Induced Draft Fans  

E-Print Network (OSTI)

Studies of 10 asphalt plants in the Intermountain Region have identified average ID fan energy savings of 68% by controlling airflow using Variable Frequency Drives (VFDs) on the fan motors in place of damper control (inlet or outlet). Average paybacks were 3-5 years before utility incentives. In the 10 plants evaluated, the ID fans accounted for as much as 30% of the total plant electrical consumption. In the majority of these plants the outlet dampers were typically 50%-60% closed. Fan motors ranged from 200 Hp to 500 Hp. With approximately 3,600 existing asphalt plants in operation across the United States, a large opportunity for retrofits exists. Working with manufacturers and owners, a new standard can be established for installing VFDs on all plants.

Anderson, G. R.; Case, P. L.; Lowery, J.

2005-01-01T23:59:59.000Z

59

Flotation behavior of digested asphalt ridge tar sands  

SciTech Connect

The hot water process for Utah tar sands differs from that used for Canadian tar sands due to inherent differences in respective bitumen viscosities and the nature of bitumen-sand association. Although contact angle measurements of solvent extracted Asphalt Ridge bitumen indicated moderate hydrophobicity, air bubble attachment to the bitumen concentrate is not possible. This suggests that flotation separation is dependent on air bubble entrapment. Improved separation at higher flotation temperatures was due to the decrease in bitumen viscosity. 16 refs.

Smith, R.J.; Miller, J.D.

1981-12-01T23:59:59.000Z

60

Phosphogypsum slag aggregate-based asphaltic concrete mixes  

Science Conference Proceedings (OSTI)

Phosphogypsum is a by-product from the production of phosphoric acid used in the fertilizer and chemical industries. Large production rates and problems associated with its stockpiling have led researchers to seek alternative uses for phosphogypsum, primarily as a construction material. One such use is the extraction of sulfur dioxide for the production of sulfuric acid, a process that also generates a by-product slag aggregate. This study investigated the feasibility of using this slag aggregate in asphaltic concrete binder course mixes. The physical properties of the slag aggregate, such as gradation, specific gravity, absorption, unit weight, and void content, were determined, as well as its durability and environmental characteristics. The Marshall mix design method was used to obtain the optimum asphalt content for this aggregate, while moisture susceptibility was examined using the boiling and modified Lottman tests. Indirect tensile, resilient modulus, and dynamic creep tests were performed on the mix to evaluate its performance potential. The results of the study indicate that phosphogypsum-based slag aggregate can be successfully employed in asphaltic concrete binder course mixtures.

Foxworthy, P.T. [Terracon Consultants, Inc., Lenexa, KS (United States); Nadimpalli, R.S.; Seals, R.K. [Louisiana State Univ., Baton Rouge, LA (United States)

1996-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Bibliography of work on the heterogeneous photocatalytic removal of hazardous compounds from water and air: Update Number 1 to June, 1995  

DOE Green Energy (OSTI)

This report is an update of a bibliography, published in May, 1994, of research performed on the photocatalytic oxidation of organic or inorganic compounds in air or water and on the photocatalytic reduction of metal-containing ions in water. The general focus of the research is on removing hazardous contaminants from air water to meet environmental or health regulations. The processes covered are based on the application of heterogeneous photocatalysts. The current state-of-the-art in catalysts are forms of titanium dioxide or modifications of titanium dioxide, but work on other heterogeneous catalysts is also included in this compilation. This update contains 574 references, most published between January, 1993 and June, 1995, but some references are from earlier work that were not included in the previous report. A new section has been added which gives information about companies that are active in providing products based on photocatalytic processes or that can provide pilot, demonstration, or commercial-scale water- or air-treatment systems. Key words, assigned by the author of this report, have been included with the citations in the listing of the bibliography.

Blake, D.M.

1995-11-01T23:59:59.000Z

62

Heat Transfer Analysis of Asphalt Concrete Pavement Based on Snow Melting  

Science Conference Proceedings (OSTI)

On the basis of Wuhan district weather conditions of January 5, 2010, heat transfer mechanism of Beijing-Zhuhai Expressway Hubei section of asphalt concrete pavement based on snow melting is analyzed and the model of heat transmission is established. ... Keywords: asphalt concrete pavement, ground-source heat, pump, deicing and snow melting, heat flux

Yan-ping Tu; Jie Li; Chang-sheng Guan

2010-06-01T23:59:59.000Z

63

Evaluation of asphalt-rubber interlayers. (Revised). Final research report, September 1986-September 1992  

SciTech Connect

The report presents the field performance results of three asphalt-rubber interlayer test roads in terms of the effectiveness of the interlayer at reducing the rate of reflection cracking. Several variables were included in the field experiments: concentration of rubber, binder application rate, type or source of rubber, and digestion (or mixing) time of asphalt and rubber. Control sections were made up of no interlayer and interlayer binders of polymer-modified asphalt and conventional asphalt cement. Results of the statistical analyses of the data indicated that, in general, asphalt-rubber interlayers are more effective at reducing reflection cracking than no interlayer at all. Asphalt-rubber also peerformed better than control sections composed of asphalt cement interlayers and polymer-modified interlayers except in one case where the interlyaer was composed of a double application of asphalt cement/aggregate. The data also indicated that higher binder application rates lead to imnproved cracking resistance; however, on many test sections, excessively high binder application rates caused flushing at the pavement surface.

Estakhri, C.K.; Pendleton, O.; Lytton, R.L.

1994-02-01T23:59:59.000Z

64

New Cool Roof Coatings and Affordable Cool Color Asphalt  

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

New Cool Roof Coatings and New Cool Roof Coatings and Affordable Cool Color Asphalt Shingles Meng-Dawn Cheng Oak Ridge National Laboratory chengmd@ornl.gov; 865-241-5918 April 4, 2013 PM: Andre Desjarlais PI: Meng-Dawn Cheng, Ph.D. David Graham, Ph.D. Sue Carroll Steve Allman Dawn Klingeman Susan Pfiffner, Ph.D. (FY12) Karen Cheng (FY12) Partner: Joe Rokowski (Dow) Roof Testing Facility at ORNL Building Technologies Research and Integration Center 2 | Building Technologies Office eere.energy.gov * Building accounted for 41% of the US energy consumption in 2010 greater than either transportation (28%) or industry (31%).

65

New Cool Roof Coatings and Affordable Cool Color Asphalt  

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

New Cool Roof Coatings and New Cool Roof Coatings and Affordable Cool Color Asphalt Shingles Meng-Dawn Cheng Oak Ridge National Laboratory chengmd@ornl.gov; 865-241-5918 April 4, 2013 PM: Andre Desjarlais PI: Meng-Dawn Cheng, Ph.D. David Graham, Ph.D. Sue Carroll Steve Allman Dawn Klingeman Susan Pfiffner, Ph.D. (FY12) Karen Cheng (FY12) Partner: Joe Rokowski (Dow) Roof Testing Facility at ORNL Building Technologies Research and Integration Center 2 | Building Technologies Office eere.energy.gov * Building accounted for 41% of the US energy consumption in 2010 greater than either transportation (28%) or industry (31%).

66

Bibliography of Work on the Heterogeneous Photocatalytic Removal of Hazardous Compounds from Water and Air--Update Number 4 to October 2001  

DOE Green Energy (OSTI)

This report is the fifth in a series of bibliographies of work on the photocatalytic oxidation of organic or inorganic compounds in air or water and on the photocatalytic reduction of inorganic compounds in water. This search contains information extracted from 1149 new references to papers, books, and reports from searches conducted between October 1996 and April 2001.

Blake, D.

2001-11-19T23:59:59.000Z

67

Development of superior asphalt recycling agency: Phase 1, Technical feasibility. Technical progress report  

SciTech Connect

About every 12 years, asphalt roads must be reworked, and this is usually done by placing thick layers (hot-mix overlays) of new material on top of failed material, resulting in considerable waste of material and use of new asphalt binder. A good recycling agent is needed, not only to reduce the viscosity of the aged material but also to restore compatibility. Objective is to establish the technical feasibility (Phase I) of determining the specifications and operating parameters for producing high quality recycling agents which will allow most/all the old asphalt-based road material to be recycled. It is expected that supercritical fractionation can be used. The advanced road aging simulation procedure will be used to study aging of blends of old asphalt and recycling agents.

Bullin, J.A.; Glover, C.J.; Davison, R.R.; Lin, Moon-Sun; Chaffin, J.; Liu, Meng; Eckhardt, C.

1996-04-01T23:59:59.000Z

68

Touch and Step Voltage Measurements on Field Installed Ground Grid Overlaid with Gravel and Asphalt Beds  

Science Conference Proceedings (OSTI)

Gravel and asphalt are commonly used as surfacing materials in and around substations. Both the electrical characteristics of the surfacing material and its moisture condition substantially affect the exposure (step, touch) voltage and the resulting current. This project evaluates the effects of various types of surfacing materials (three gravel types and asphalt) and conditions (dry and wet) on step and touch voltages in and around substations.

2010-12-21T23:59:59.000Z

69

Lignite slime as activator in production of oxidized asphalts  

Science Conference Proceedings (OSTI)

The possibility of activation of the oxidation of straight-run resids to asphalts by the addition of lignite slimes obtained in the liquefaction of coals of the Kansk-Achinsk basin was studied on the basis of a hypothesis formulated with due regard for the principles of physicochemical mechanics of petroleum disperse systems. A reduction of the air bubble size in the oxidizing vessel should lead to an increase in the total surface of oxidation and hence to a shortening of the time required for oxidation of the feed. A straight-run vacuum resid from mixed West Siberian and Ukhta crudes was used. The resid was oxidized with and without the addition of slime.

Gureev, A.A.; Gorlov, E.G.; Leont'eva, O.B.; Zotova, O.V.

1988-03-01T23:59:59.000Z

70

Prediction of Reflection Cracking in Hot Mix Asphalt Overlays  

E-Print Network (OSTI)

Reflection cracking is one of the main distresses in hot-mix asphalt (HMA) overlays. It has been a serious concern since early in the 20th century. Since then, several models have been developed to predict the extent and severity of reflection cracking in HMA overlays. However, only limited research has been performed to evaluate and calibrate these models. In this dissertation, mechanistic-based models are calibrated to field data of over 400 overlay test sections to produce a design process for predicting reflection cracks. Three cracking mechanisms: bending, shearing traffic stresses, and thermal stress are taken into account to evaluate the rate of growth of the three increasing levels of distress severity: low, medium, and high. The cumulative damage done by all three cracking mechanisms is used to predict the number of days for the reflection crack to reach the surface of the overlay. The result of this calculation is calibrated to the observed field data (severity and extent) which has been fitted with an S-shaped curve. In the mechanistic computations, material properties and fracture-related stress intensity factors are generated using efficient Artificial Neural Network (ANN) algorithms. In the bending and shearing traffic stress models, the traffic was represented by axle load spectra. In the thermal stress model, a recently developed temperature model was used to predict the temperature at the crack tips. This process was developed to analyze various overlay structures. HMA overlays over either asphalt pavement or jointed concrete pavement in all four major climatic zones are discussed in this dissertation. The results of this calculated mechanistic approach showed its ability to efficiently reproduce field observations of the growth, extent, and severity of reflection cracking. The most important contribution to crack growth was found to be thermal stress. The computer running time for a twenty-year prediction of a typical overlay was between one and four minutes.

Tsai, Fang-Ling

2010-12-01T23:59:59.000Z

71

A Coupled Micromechanical Model of Moisture-Induced Damage in Asphalt Mixtures: Formulation and Applications  

E-Print Network (OSTI)

The deleterious effect of moisture on the structural integrity of asphalt mixtures has been recognized as one of the main causes of early deterioration of asphalt pavements. This phenomenon, usually referred to as moisture damage, is defined as the progressive loss of structural integrity of the mixture that is primarily caused by the presence of moisture in liquid or vapor state. Moisture damage is associated with the development of different physical, mechanical, and chemical processes occurring within the microstructure of the mixture at different intensities and rates. Although there have been important advancements in identifying and characterizing this phenomenon, there is still a lack of understanding of the damage mechanisms occurring at the microscopic level. This situation has motivated the research work reported in this dissertation. The main objective of this dissertation is to formulate and apply a numerical micromechanical model of moisture-induced damage in asphalt mixtures. The model focuses on coupling the effects of moisture diffusion—one of the three main modes of moisture transport within asphalt mixtures—with the mechanical performance of the microstructure. Specifically, the model aims to account for the effect of moisture diffusion on the degradation of the viscoelastic bulk matrix of the mixture (i.e., cohesive degradation) and on the gradual deterioration of the adhesive bonds between the aggregates and the asphalt matrix (i.e., adhesive degradation). The micromechanical model was applied to study the role of some physical and mechanical properties of the constitutive phases of the mixtures on the susceptibility of the mixture to moisture damage. The results from this analysis suggest that the diffusion coefficients of the asphalt matrix and aggregates, as well as the bond strength of the aggregate-matrix interface, have the most influence on the moisture susceptibility of the mixtures. The micromechanical model was further used to investigate the influence of the void phase of asphalt mixtures on the generation of moisture-related deterioration processes. Two different probabilistic-based approaches were used to accomplish this objective. In the first approach, a volumetric distribution of air voids sizes measured using X-Ray Computed Tomography in a dense-graded asphalt mixture was used to generate probable void structures in a microstructure of an asphalt mixture. In the second approach, a stochastic modeling technique based on random field theory was used to generate probable air voids distributions of the mixture. In this second approach, the influence of the air voids was accounted for by making the physical and mechanical properties of the asphalt matrix dependent on probable voids distributions. Although both approaches take into consideration the characteristics of the air void phase on the mechanical response of the mixtures subjected to moist environments, the former explicitly introduces the air phase within the microstructure while the latter indirectly includes its effects by modifying the material properties of the bulk matrix. The results from these simulations demonstrated that the amount, variability and location of air voids are decisive in determining the moisture-dependent performance of asphalt mixtures. The results from this dissertation provide new information on the kinetics of moisture damage mechanisms in asphalt mixtures. In particular, the results obtained from applying the micromechanical model permitted identification of the relative influence of the characteristics of the constitutive phases of a mixture on its moisture-related mechanical performance. This information can be used as part of design methodologies of asphalt mixtures, and/or as an input in life-cycle analysis models and maintenance programs of road infrastructure.

Caro Spinel, Silvia

2009-12-01T23:59:59.000Z

72

Development of superior asphalt recycling agents. Phase 1, Technical feasibility. Final technical progress report  

Science Conference Proceedings (OSTI)

After an introduction and a literature survey in Chap. 1, Chap. 2 describes the tasks, together with objectives and important results obtained for each task throughout the entire project. Chaps. 3 thru 7 detail work in developing a qualitative and quantitative knowledge of asphalt oxidation, composition dependence of asphalt properties, and guidelines for producing superior asphalt binders through composition control. They also detail the development of a kinetic model for asphalt oxidative aging and present an understanding of the composition dependence of asphalt oxidation as well as other performance-related properties. Chaps. 8 and 9 compare the aging performance of recycled blends produced using commercial recycling agents and industrial supercritical fractions as rejuvenating agents. Oxidative aging of the recycled blends were evaluated along with the performance of the recycled blends in terms of the strategic highway research program performance grading procedure. Chap. 10 summarizes the work completed in the areas of processing schemes development, projection updates, and scale-up and commercialization plans.

Bullin, J.A.; Davison, R.R.; Glover, C.J.; Chaffin, J.; Liu, M.; Madrid, R.

1997-07-01T23:59:59.000Z

73

Microstructural Characterization of the Chemo-mechanical Behavior of Asphalt in Terms of Aging and Fatigue Performance Properties  

E-Print Network (OSTI)

The study of asphalt chemo-mechanics requires a basic understanding of the physical properties and chemical composition of asphalt and how these properties are linked to changes in performance induced by chemical modifications. This work uniquely implements the framework of chemo-mechanics by investigating two types of chemical modification processes, natural (oxidative aging) and synthetic (chemical doping) as they relate not only to macro-scale properties of asphalt binder but also to the asphalt microstructure and nanorheology. Furthermore, this study demonstrates the application of atomic force microscopy (AFM) imaging and the extraction of nano-scale engineering properties, i.e. elastic modulus, relaxation modulus, and surface energy, as a method to predict performance related to the fatigue characteristics of asphalt binders by modeling intrinsic material flaws present amongst phase interfaces. It was revealed that oxidative aging induces substantial microstructural changes in asphalt, including variations in phase structure, phase properties, and phase distribution. It has also been shown that certain asphalt chemical parameters have a consistent and measureable effect on the asphalt microstructure that is observed with AFM. In fact, particular phases that emerged via chemical doping revealed a surprising correlation between oxidative aging and the saturates chemical parameter of asphalt in terms of how they explicitly impact durability and performance of asphalt. By implementing a crack initiation model – which requires measureable microstructural characteristics as an input parameter – it was found that microstructural flaws (depending on the extremity) can have a more profound impact on asphalt performance than the properties of the material located between the flaws. It was also discovered by comparing the findings to performance data in the Strategic Highway Research Program’s (SHRP’s) Materials Reference Library (MRL), that the crack initiation model predicts very similar performance as the SHRP’s distress resistance indicators. Overall, this body of work yields improved input values for asphalt prediction models and serves as the basis for ongoing studies in the areas of asphalt chemical mapping, modeling of nano-damage, and nano-modification using AFM.

Allen, Robert Grover

2013-05-01T23:59:59.000Z

74

Ion Removal  

INL’s ion removal technology leverages the ability of phosphazene polymers discriminate between water and metal ions, which allows water to pass ...

75

A comparison of the fracture properties of conventional and polymer-modified two-layer asphalt concrete overlay systems  

E-Print Network (OSTI)

The problem of reflection cracking through the conventional asphalt concrete overlays has increased the need to find new materials which could resist cracking or fracture more effectively. It is for this reason that polymers (Styrelo are added to the neat asphalt to improve the fracture resisting properties of asphalt concrete. In this study three different asphalt concrete mixtures with and without polymer (Styrelf) were used to study their fracture toughness. With four different binders and different combinations of mixtures, 18 different overlay systems were tested for their fracture toughness. Each overlay was made up of two different layers with asphalt rich sand anti-fracture (SAF) mixture as the bottom layer. Fracture mechanics concepts were used to compare the fracture properties of polymer (Styrelo modified asphalt concrete with the corresponding conventional neat asphalt concrete. Rate of crack growth is correlated with the energy line J*-integral. Crack growth rates were determined from laboratory experiments conducted on TTI overlay tester. Analysis of the experimental results showed that crack growth rate and J*-integral are correlated. In this study it was observed that the relation between the fracture material constants log(A) and (n) is not linear. A new fracture material constant (S) relating to crack speed was developed. The relationship between log(A) and (n) was found to be linear when combined with constant (S). Results showed that this new material constant (S) could lead to a better characterization of fracture toughness. Crack speed when calculated using (S) has shown better correlation with the observed experimental fatigue life. It is speculated that this new material constant (S) could be related to healing of the asphalt concrete or the plasticity effects due to unloading of the sample in overlay test.

Reddy, Praveena Gutha

1996-01-01T23:59:59.000Z

76

Surface roughness effects on the solar reflectance of cool asphalt shingles  

Science Conference Proceedings (OSTI)

We analyze the solar reflectance of asphalt roofing shingles that are covered with pigmented mineral roofing granules. The reflecting surface is rough, with a total area approximately twice the nominal area. We introduce a simple analytical model that relates the 'micro-reflectance' of a small surface region to the 'macro-reflectance' of the shingle. This model uses a mean field approximation to account for multiple scattering effects. The model is then used to compute the reflectance of shingles with a mixture of different colored granules, when the reflectances of the corresponding mono-color shingles are known. Simple linear averaging works well, with small corrections to linear averaging derived for highly reflective materials. Reflective base granules and reflective surface coatings aid achievement of high solar reflectance. Other factors that influence the solar reflectance are the size distribution of the granules, coverage of the asphalt substrate, and orientation of the granules as affected by rollers during fabrication.

Akbari, Hashem; Berdahl, Paul; Akbari, Hashem; Jacobs, Jeffry; Klink, Frank

2008-02-17T23:59:59.000Z

77

Development of asphalts and pavements using recycled tire rubber. Phase 1, Technical feasibility. Technical progress report, September 1, 1994--August 31, 1995  

Science Conference Proceedings (OSTI)

About 285 million tires are discarded every year; less than 100 million are currently being recycled, with the rest being placed in landfills and other waste sites. A solution to reduce the littering of the environment is to use ground tire rubber in road construction. Currently, about 27 million tons of asphalt are used each year in road construction and maintenance of the country`s 2 million miles of roads. If all of the waste tire rubber could be combined with asphalt in road construction, it would displace less than 6% of the total asphalt used each year, yet could save about 60 trillion Btus annually. Purpose of this project is to provide data needed to optimize the performance of rubber-asphalt concretes. The first phase is to develop asphalts and recycling agents tailored for compatibility with ground tire rubber. Chapter 2 presents results on Laboratory Testing and Evaluation: fractionate asphalt material, reblending for aromatic asphalts, verifying optimal curing parameters, aging of blends, and measuring ductilities of asphalt-rubber binders. Chapter 3 focuses on Evaluating Mixture Characteristics (modified binders). Chapter 4 covers Adhesion Test Development (water susceptibility is also covered). The final chapter focuses on the Performance/Economic Update and Commercialization Plan.

Bullin, J.A.; Davison, R.R.; Glover, C.J. [and others

1996-06-01T23:59:59.000Z

78

A. SCOPE METHOD OF TEST FOR DETERMINING THEORETICAL MAXIMUM SPECIFIC GRAVITY AND DENSITY OF HOT MIX ASPHALT  

E-Print Network (OSTI)

This test method provides procedures for determining the theoretical maximum specific gravity (also known as Rice specific gravity) and density of uncompacted hot mix asphalt (HMA) at 77?F using the weighing in air method. A supplemental dry back procedure is provided for reclaimed asphalt pavement (RAP) and for HMA where combined virgin aggregate water absorption is 2.0 % or more determined by California Test 206 and California Test 207. The theoretical maximum specific gravities and densities of HMA are intrinsic properties whose values are influenced by the composition of the mixtures in terms of types and amounts of aggregates and asphalt binder materials. They are: 1. Used to calculate values for percent air voids in compacted HMA. 2. Used to establish target values for the compaction of HMA. 3. Essential when calculating the amount of binder absorbed by the internal porosity of the individual aggregate particles in HMA. B. REFERENCES

C. Apparatus

2010-01-01T23:59:59.000Z

79

Experimental Study on Shear Fatigue Behavior and Stiffness Performance of Warm Mix Asphalt by adding Synthetic Wax  

E-Print Network (OSTI)

Synthetic waxes produced by standard and registered processes may be used to manufacture Warm Mix Asphalt (WMA), which is a modified asphalt concrete produced, applied and compacted at temperatures below those typically required. This feature leads to environmental benefits, such as reduced energy consumption, gas and fume emissions, as well as to economic/operational advantages, such as lower production costs and greater hauling distances for extended construction seasons with tighter schedules. The present article serves to compare the mechanical performance of a WMA produced by adding synthetic wax with a traditional Hot Mix Asphalt (HMA) specimen, in terms of shear fatigue response and both complex and stiffness moduli. The experimental results and related modeling work demonstrate that adding synthetic wax into the WMA composition does not hinder either the destructive or non-destructive performance of an HMA, and this finding is corroborated by respectively measuring fatigue life and stiffness.

Christophe Petit; Anne Millien; Francesco Canestrari; Valter Pannunzio; Amadeo Virgili

2012-03-13T23:59:59.000Z

80

The use of sulfer modified bottom ash (SMBA) as an aggregate in asphaltic mixtures  

E-Print Network (OSTI)

Of the 20 million tons of bottom ash and boiler slag generated annually in the United States less than 40 percent is used. The eastern half of Texas is served by 18 coal burning electric power generating plants which produce approximately 3.8 million tons of bottom ash each year. This is also the section of the state in which the sources of quality aggregates are either few. dwindling or nonexistent. While a small fraction of the bottom ash is utilized, the rest is delegated to landfills or on-site disposal areas. Increasing attention is being given to development of new, high-volume uses for this safe and readily available by-product. One such use is as an aggregate in road construction. The use of bottom ash as an aggregate for both roadway surfaces and base courses has been limited due to its absorbency and friability. The former tends to increase asphalt binder demand while the latter adversely affects its ability to withstand the crushing effects of traffic loads. On the other hand, bottom ash is lighter in weight and generally much cheaper than conventional quality aggregates such as limestone, sand and gavel. This research was designed to up-firade the load-bearing characteristics of bottom ash and maximize its use 'in asphaltic concrete roadway mixtures through the use of sulfur. The process essentially coats the ash with liquid sulfur which upon cooling fills the voids on the surface of the particles while increasing their crush resistance. The results of this investigation indicate that asphaltic concrete mix designs in which bottom ash represents from 5 0 to I 00 percent of the aggregate fraction can be achieved.

Chimakurthy, Harshavardhan

1998-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Process for removing sulfur from coal  

DOE Patents (OSTI)

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

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

1983-08-11T23:59:59.000Z

82

Development of a Prediction Model for Skid Resistance of Asphalt Pavements  

E-Print Network (OSTI)

The skid resistance of asphalt pavement is a major characteristic that determines the driving safety on a road, especially under wet surface conditions. Skid resistance is primarily a function of the microtexture and macrotexture of a pavement surface. Microtexture is influenced by aggregate surface characteristics and is required to disrupt the continuity of surface water film and attain frictional resistance between the tire and the pavement surface. Macrotexture is affected mostly by mixture design or aggregate gradation and contributes to skid resistance by providing drainage paths of water that can be otherwise trapped between a tire and a pavement surface. The increase in macrotexture contributes to preventing hydroplaning and improving wet frictional resistance, particularly at high speeds. While much research has been conducted in the past to identify material factors that affect skid resistance, there is still a need to develop a model for predicting asphalt pavement skid resistance as a function of mixture characteristics and traffic level. The purpose of this study was to develop such a model based on extensive laboratory experiments and field measurements involving different mixture types and aggregate sources. The model incorporates functions that describe the resistance of aggregates to polishing and aggregate size distribution. The aggregate resistance to polishing was quantified by measuring aggregate texture using the Aggregate Imaging System (AIMS) before and after polishing in the Micro-Deval device. The analysis in this dissertation demonstrates how this model can be used to design mixtures and classify aggregates that provide desirable skid resistance levels.

Rezaei, Arash

2010-12-01T23:59:59.000Z

83

Physical stability of asphalt emulsion admix seal radon barrier for uranium mill tailings  

SciTech Connect

Pacific Northwest Laboratory, is investigating the use of an asphalt emulsion admix seal to reduce the release of radon from uranium mill tailings. A key requirement of any cover system is its long-term stability; the cover must withstand failure over very long periods of time. An important determinant of overall cover system stability is the integrity of the 6.35-cm (2.5-in.) thick asphalt admix seal. Therefore, the physical stability of this seal was examined. The investigation considered the mechanical interaction between the tailings pile and cover. The potential effect of differential settlement of the tailings pile on the integrity of the seal system was also examined. Results indicate that the minimum span length the seal could withstand without failing is 0.34 m (1.1 ft). This assumes a differential settlement of 4.92 cm (1.94 in.) at the center resulting from the application of a 0.76-m (2.5-ft) cover. At spans greater than 0.60 m (1.97 ft), no tensile strain would develop.

Gates, T.E.

1983-09-01T23:59:59.000Z

84

Method of removal of sulfur from coal and petroleum products  

DOE Patents (OSTI)

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

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

1995-01-01T23:59:59.000Z

85

Modeling Hot Mix Asphalt Compaction Using a Thermodynamics Based Compressible Viscoelastic Model within the Framework of Multiple Natural Configurations  

E-Print Network (OSTI)

Hot mix asphalt (HMA) is a composite material that exhibits a nonlinear response that is dependent on temperature, type of loading and strain level. The properties of HMA are highly influenced by the type and amount of the constituents used and also depend on its internal structure. In such a material the variable effects of the compaction process assume a central importance in determining material performance. It is generally accepted that the theoretical knowledge about material behavior during compaction is limited and it is therefore hard to predict and manage (the effect of) a compaction process. This work makes an attempt to address such a specific need by developing a continuum model that can be adapted for simulating the compaction of hot mix asphalt (HMA) using the notion of multiple natural configurations. A thermodynamic framework is employed to study the non-linear dissipative response associated with HMA by specifying the forms for the stored energy and the rate of dissipation function for the material; a viscoelastic compressible fluid model is developed using this framework to model the compaction of hot mix asphalt. It is further anticipated that the present work will aid in the development of better constitutive models capable of capturing the mechanics of processes like compaction both in the laboratory and in the field. The continuum model developed was implemented in the finite element method, which was employed to setup a simulation environment for hot mix asphalt compaction. The finite element method was used for simulating compaction in the laboratory and in various field compaction projects.

Koneru, Saradhi

2010-08-01T23:59:59.000Z

86

Polybenzimidazole compounds  

SciTech Connect

A PBI compound that includes imidazole nitrogens, at least a portion of which are substituted with an organic-inorganic hybrid moiety. At least 85% of the imidazole nitrogens may be substituted. The organic-inorganic hybrid moiety may be an organosilane moiety, for example, (R)Me.sub.2SiCH.sub.2--, where R is selected from among methyl, phenyl, vinyl, and allyl. The PBI compound may exhibit similar thermal properties in comparison to the unsubstituted PBI. The PBI compound may exhibit a solubility in an organic solvent greater than the solubility of the unsubstituted PBI. The PBI compound may be included in separatory media. A substituted PBI synthesis method may include providing a parent PBI in a less than 5 wt % solvent solution. Substituting may occur at about room temperature and/or at about atmospheric pressure. Substituting may use at least five equivalents in relation to the imidazole nitrogens to be substituted or, preferably, about fifteen equivalents.

Klaehn, John R. (Idaho Falls, ID); Peterson, Eric S. (Idaho Falls, ID); Wertsching, Alan K. (Idaho Falls, ID); Orme, Christopher J. (Shelley, ID); Luther, Thomas A. (Idaho Falls, ID); Jones, Michael G. (Pocatello, ID)

2010-08-10T23:59:59.000Z

87

Polybenzimidazole compounds  

DOE Patents (OSTI)

A PBI compound includes imidazole nitrogens at least a portion of which are substituted with a moiety containing a carbonyl group, the substituted imidazole nitrogens being bonded to carbon of the carbonyl group. At least 85% of the nitrogens may be substituted. The carbonyl-containing moiety may include RCO--, where R is alkoxy or haloalkyl. The PBI compound may exhibit a first temperature marking an onset of weight loss corresponding to reversion of the substituted PBI that is less than a second temperature marking an onset of decomposition of an otherwise identical PBI compound without the substituted moiety. The PBI compound may be included in separatory media. A substituted PBI synthesis method may include providing a parent PBI in a less than 5 wt % solvent solution. Substituting may use more than 5 equivalents in relation to the imidazole nitrogens to be substituted.

Klaehn, John R. (Idaho Falls, ID); Peterson, Eric S. (Idaho Falls, ID); Orme, Christopher J. (Shelley, ID); Jones, Michael G. (Chubbuck, ID); Wertsching, Alan K. (Idaho Falls, ID); Luther, Thomas A. (Idaho Falls, ID); Trowbridge, Tammy L. (Idaho Falls, ID)

2011-11-22T23:59:59.000Z

88

The Effects of Using Alkali-Silica Reaction Affected Recycled Concrete Aggregate in Hot Mix Asphalt  

E-Print Network (OSTI)

The effects of using alkali-silica reaction (ASR) affected recycled concrete aggregate (ASR-RCA) in hot mix asphalt (HMA) were investigated in this study. Dilatometer and modified beam tests were performed to determine the possibility of new ASR occurring in reactive aggregates within the HMA or re-expansion of existing gel. The Lottman test and micro-calorimeter were used to determine the moisture susceptibility of HMA made with ASR-RCA. A differential scanning calorimeter (DSC) with thermogravimetric analysis (TGA) was used to evaluate the drying of an artificial gel and x-ray diffraction (XRD) was used to check for the potential presence of gel in the filler fraction of the ASR-RCAs. Micro-deval and freeze-thaw tests were evaluated for their potential to indicate the presence of excess micro-cracks or ASR gel. Expansion testing indicated that both ASR-RCAs were still reactive with 0.5 N NaOH solution saturated with calcium hydroxide (CH) at 60 degrees C. Dilatometer testing of HMA specimens in NaOH CH solution at 60 degrees C indicated a reaction between the asphalt binder and the solution, but little, if any, ASR. The lack of expansion in the modified beam test supports the binder-solution interaction. However, dilatometer testing in deicer solution at the same temperature indicated that some ASR may have occurred along with the primary binder-solution interaction. The volume change characteristics associated with the binder-solution interaction with and without ASR was supported by the change in pH and alkali concentration of the test solution. DSC/TGA testing indicated that the artificial gel dehydrated at approximately 100 degrees C. XRD analysis of the filler indicated that some gel may have accumulated in this fraction. Moisture damage testing indicated good resistance to moisture damage by HMA mixtures made with ASR-RCA especially compared to a virgin siliceous aggregate. Micro-deval and freeze-thaw tests can detect the presence of micro-cracks due to ASR in ASR-RCAs as higher mass loss than the virgin aggregate. The potential distress mechanisms that may occur when using ASR-RCA in an HMA pavement were identified. Results obtained using accelerated laboratory conditions were extrapolated based on anticipated field conditions. Guidelines for the mitigation of potential distresses in HMA made with ASR-RCA are presented.

Geiger, Brian James

2010-08-01T23:59:59.000Z

89

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

90

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

91

Catalyst regeneration process including metal contaminants removal  

DOE Patents (OSTI)

Spent catalysts removed from a catalytic hydrogenation process for hydrocarbon feedstocks, and containing undesired metals contaminants deposits, are regenerated. Following solvent washing to remove process oils, the catalyst is treated either with chemicals which form sulfate or oxysulfate compounds with the metals contaminants, or with acids which remove the metal contaminants, such as 5-50 W % sulfuric acid in aqueous solution and 0-10 W % ammonium ion solutions to substantially remove the metals deposits. The acid treating occurs within the temperature range of 60.degree.-250.degree. F. for 5-120 minutes at substantially atmospheric pressure. Carbon deposits are removed from the treated catalyst by carbon burnoff at 800.degree.-900.degree. F. temperature, using 1-6 V % oxygen in an inert gas mixture, after which the regenerated catalyst can be effectively reused in the catalytic process.

Ganguli, Partha S. (Lawrenceville, NJ)

1984-01-01T23:59:59.000Z

92

A novel technique for the production of cool colored concrete tile and asphalt shingle roofing products  

SciTech Connect

The widespread use of solar-reflective roofing materials can save energy, mitigate urban heat islands and slow global warming by cooling the roughly 20% of the urban surface that is roofed. In this study we created prototype solar-reflective nonwhite concrete tile and asphalt shingle roofing materials using a two-layer spray coating process intended to maximize both solar reflectance and factory-line throughput. Each layer is a thin, quick-drying, pigmented latex paint based on either acrylic or a poly(vinylidene fluoride)/acrylic blend. The first layer is a titanium dioxide rutile white basecoat that increases the solar reflectance of a gray-cement concrete tile from 0.18 to 0.79, and that of a shingle surfaced with bare granules from 0.06 to 0.62. The second layer is a 'cool' color topcoat with weak near-infrared (NIR) absorption and/or strong NIR backscattering. Each layer dries within seconds, potentially allowing a factory line to pass first under the white spray, then under the color spray. We combined a white basecoat with monocolor topcoats in various shades of red, brown, green and blue to prepare 24 cool color prototype tiles and 24 cool color prototypes shingles. The solar reflectances of the tiles ranged from 0.26 (dark brown; CIELAB lightness value L* = 29) to 0.57 (light green; L* = 76); those of the shingles ranged from 0.18 (dark brown; L* = 26) to 0.34 (light green; L* = 68). Over half of the tiles had a solar reflectance of at least 0.40, and over half of the shingles had a solar reflectance of at least 0.25.

Levinson, Ronnen; Akbari, Hashem; Berdahl, Paul; Wood, Kurt; Skilton, Wayne; Petersheim, Jerry

2009-11-20T23:59:59.000Z

93

Turbomachinery debris remover  

DOE Patents (OSTI)

An apparatus for removing debris from a turbomachine. The apparatus includes housing and remotely operable viewing and grappling mechanisms for the purpose of locating and removing debris lodged between adjacent blades in a turbomachine.

Krawiec, Donald F. (Pittsburgh, PA); Kraf, Robert J. (North Huntingdon, PA); Houser, Robert J. (Monroeville, PA)

1988-01-01T23:59:59.000Z

94

Graphitic packing removal tool  

DOE Patents (OSTI)

Graphitic packing removal tools are described for removal of the seal rings in one piece from valves and pumps. The packing removal tool has a cylindrical base ring the same size as the packing ring with a surface finish, perforations, knurling or threads for adhesion to the seal ring. Elongated leg shanks are mounted axially along the circumferential center. A slit or slits permit insertion around shafts. A removal tool follower stabilizes the upper portion of the legs to allow a spanner wrench to be used for insertion and removal.

Meyers, K.E.; Kolsun, G.J.

1996-12-31T23:59:59.000Z

95

Regenerable Hydrogen Chloride Removal Sorbent and Regenerable Multifunctional Hydrogen Sulfide and Hydrogen Chloride Removal Sorbent for High Temperature Gas Streams  

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

Hydrogen Chloride and Hydrogen Sulfide Hydrogen Chloride and Hydrogen Sulfide Removal Sorbents for High Temperature Gas Streams Opportunity The Department of Energy's National Energy Technology Laboratory (NETL) is seeking licensing partners interested in implementing United States Patent Number 7,767,000 entitled "Regenerable Hydrogen Chloride Removal Sorbent and Regenerable Multifunctional Hydrogen Sulfide and Hydrogen Chloride Removal Sorbent for High Temperature Gas Streams." Disclosed in this patent is the invention of a unique regenerable sorbent process that can remove contaminants from gas produced by the gasification of fossil fuels. Specifically, the process removes hydrogen chloride by using the regenerable sorbent and simultaneously extracts hydrogen chloride compounds and hydrogen

96

Bismaleimide compounds  

DOE Patents (OSTI)

Bismaleimides of the formula ##STR1## wherein R.sub.1 and R.sub.2 each independently is H, C.sub.1-4 -alkyl, C.sub.1-4 -alkoxy, C1 or Br, or R.sub.1 and R.sub.2 together form a fused 6-membered hydrocarbon aromatic ring, with the proviso that R.sub.1 and R.sub.2 are not t-butyl or t-butoxy; X is O, S or Se; n is 1-3; and the alkylene bridging group, optionally, is substituted by 1-3 methyl groups or by fluorine, form polybismaleimide resins which have valuable physical properties. Uniquely, these compounds permit extended cure times, i.e., they remain fluid for a time sufficient to permit the formation of a homogeneous melt prior to curing.

Adams, Johnnie E. (Grandview, MO); Jamieson, Donald R. (Merriam, KS)

1986-01-14T23:59:59.000Z

97

Novel amine-based presursor compounds and composite membranes thereof  

DOE Patents (OSTI)

Novel amine-based precursor compounds comprising the condensation products of dialkylenetriamine and alpha, beta-unsaturated acid halides are disclosed, as well as composite membranes containing such compounds, the membranes being useful in RO-type processes for desalination and the removal of low molecular weight organic compounds such as phenols and carboxylic acids.

Lee, Eric K. L. (Wilmington, DE); Tuttle, Mark E. (Bend, OR)

1989-01-01T23:59:59.000Z

98

Low Temperature Sorbents for Removal of Sulfur Compounds from...  

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

less expensive sorbent to manufacture and maintain Applications * Power generation systems * Natural gas and oil production processes * Coal gasification and oil shale production...

99

Pyrolitic Uranium Compound (PYRUC)  

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

Pyrolitic Uranium Compound Pyrolitic Uranium Compound (PYRUC) PYRolitic Uranium Compound (PYRUC) is a shielding material consisting of depleted uranium UO2 or UC in either pellet...

100

Uranium and Its Compounds  

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

and Its Compounds Uranium and Its Compounds line line What is Uranium? Chemical Forms of Uranium Properties of Uranium Compounds Radioactivity and Radiation Uranium Health Effects...

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Device for removing blackheads  

DOE Patents (OSTI)

A device for removing blackheads from pores in the skin having a elongated handle with a spoon shaped portion mounted on one end thereof, the spoon having multiple small holes piercing therethrough. Also covered is method for using the device to remove blackheads.

Berkovich, Tamara (116 N. Wetherly Dr., Suite 115, Los Angeles, CA)

1995-03-07T23:59:59.000Z

102

Silica Scaling Removal Process  

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

Silica Scaling Removal Process Silica Scaling Removal Process Silica Scaling Removal Process Scientists at Los Alamos National Laboratory have developed a novel technology to remove both dissolved and colloidal silica using small gel particles. Available for thumbnail of Feynman Center (505) 665-9090 Email Silica Scaling Removal Process Applications: Cooling tower systems Water treatment systems Water evaporation systems Potential mining applications (produced water) Industry applications for which silica scaling must be prevented Benefits: Reduces scaling in cooling towers by up to 50% Increases the number of cycles of concentration substantially Reduces the amount of antiscaling chemical additives needed Decreases the amount of makeup water and subsequent discharged water (blowdown) Enables considerable cost savings derived from reductions in

103

Utilize Cementitious High Carbon Fly Ash (CHCFA) to Stabilize Cold In-Place Recycled (CIR) Asphalt Pavement as Base Coarse  

Science Conference Proceedings (OSTI)

The purpose of this study was to evaluate the performance of cementitious high carbon fly ash (CHCFA) stabilized recycled asphalt pavement as a base course material in a real world setting. Three test road cells were built at MnROAD facility in Minnesota. These cells have the same asphalt surface layers, subbases, and subgrades, but three different base courses: conventional crushed aggregates, untreated recycled pavement materials (RPM), and CHCFA stabilized RPM materials. During and after the construction of the three cells, laboratory and field tests were carried out to characterize the material properties. The test results were used in the mechanistic-empirical pavement design guide (MEPDG) to predict the pavement performance. Based on the performance prediction, the life cycle analyses of cost, energy consumption, and greenhouse gasses were performed. The leaching impacts of these three types of base materials were compared. The laboratory and field tests showed that fly ash stabilized RPM had higher modulus than crushed aggregate and RPM did. Based on the MEPDG performance prediction, the service life of the Cell 79 containing fly ash stabilized RPM, is 23.5 years, which is about twice the service life (11 years) of the Cell 77 with RPM base, and about three times the service life (7.5 years) of the Cell 78 with crushed aggregate base. The life cycle analysis indicated that the usage of the fly ash stabilized RPM as the base of the flexible pavement can significantly reduce the life cycle cost, the energy consumption, the greenhouse gases emission. Concentrations of many trace elements, particularly those with relatively low water quality standards, diminish over time as water flows through the pavement profile. For many elements, concentrations below US water drinking water quality standards are attained at the bottom of the pavement profile within 2-4 pore volumes of flow.

Wen, Haifang; Li, Xiaojun; Edil, Tuncer; O'Donnell, Jonathan; Danda, Swapna

2011-02-05T23:59:59.000Z

104

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

DOE Patents (OSTI)

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

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

2006-10-10T23:59:59.000Z

105

Method for the removal of elemental mercury from a gas stream  

DOE Patents (OSTI)

A method is provided to remove elemental mercury from a gas stream by reacting the gas stream with an oxidizing solution to convert the elemental mercury to soluble mercury compounds. Other constituents are also oxidized. The gas stream is then passed through a wet scrubber to remove the mercuric compounds and oxidized constituents. 7 figs.

Mendelsohn, M.H.; Huang, H.S.

1999-05-04T23:59:59.000Z

106

Method for the removal of elemental mercury from a gas stream  

DOE Patents (OSTI)

A method is provided to remove elemental mercury from a gas stream by reacting the gas stream with an oxidizing solution to convert the elemental mercury to soluble mercury compounds. Other constituents are also oxidized. The gas stream is then passed through a wet scrubber to remove the mercuric compounds and oxidized constituents.

Mendelsohn, Marshall H. (Downers Grove, IL); Huang, Hann-Sheng (Darien, IL)

1999-01-01T23:59:59.000Z

107

A method for the removal of elemental mercury from a gas stream  

DOE Patents (OSTI)

A method is provided to remove elemental mercury from a gas stream by reacting the gas stream with an oxidizing solution to convert the elemental mercury to soluble mercury compounds. Other constituents are also oxidized. The gas stream is then passed through a wet scrubber to remove the mercuric compounds and oxidized constituents.

Mendelsohn, Marshall H.; Huang, Hann-Sheng

1997-12-01T23:59:59.000Z

108

Continuous sulfur removal process  

DOE Patents (OSTI)

A continuous process for the removal of hydrogen sulfide from a gas stream using a membrane comprising a metal oxide deposited on a porous support is disclosed. 4 figures.

Jalan, V.; Ryu, J.

1994-04-26T23:59:59.000Z

109

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a combination reactor/distillation column comprising a vessel suitable for operating between 70 C and 500 C and from 0.5 to 20 atmospheres pressure; an inert distillation packing in the lower one-third of said vessel; solid acidic catalytic material such as zeolites or an acidic cation exchange resin supported in the middle one-third of said vessel; and inert distillation packing in the upper one-third of said vessel. A benzene inlet is located near the upper end of the vessel; an olefin inlet is juxtaposed with said solid acidic catalytic material; a bottoms outlet is positioned near the bottom of said vessel for removing said cumene and ethyl benzene; and an overhead outlet is placed at the top of said vessel for removing any unreacted benzene and olefin.

Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

1993-01-05T23:59:59.000Z

110

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a combination reactor/distillation column comprising a vessel suitable for operating between 70.degree. C. and 500.degree. C. and from 0.5 to 20 atmospheres pressure; an inert distillation packing in the lower one-third of said vessel; solid acidic catalytic material such as zeolites or an acidic cation exchange resin supported in the middle one-third of said vessel; and inert distillation packing in the upper one-third of said vessel. A benzene inlet is located near the upper end of the vessel; an olefin inlet is juxtaposed with said solid acidic catalytic material; a bottoms outlet is positioned near the bottom of said vessel for removing said cumene and ethyl benzene; and an overhead outlet is placed at the top of said vessel for removing any unreacted benzene and olefin.

Smith, Jr., Lawrence A. (Bellaire, TX); Arganbright, Robert P. (Seabrook, TX); Hearn, Dennis (Houston, TX)

1993-01-01T23:59:59.000Z

111

Removable feedwater sparger assembly  

DOE Patents (OSTI)

A removable feedwater sparger assembly includes a sparger having an inlet pipe disposed in flow communication with the outlet end of a supply pipe. A tubular coupling includes an annular band fixedly joined to the sparger inlet pipe and a plurality of fingers extending from the band which are removably joined to a retention flange extending from the supply pipe for maintaining the sparger inlet pipe in flow communication with the supply pipe. The fingers are elastically deflectable for allowing engagement of the sparger inlet pipe with the supply pipe and for disengagement therewith. 8 figs.

Challberg, R.C.

1994-10-04T23:59:59.000Z

112

Multi-component Removal in Flue Gas by Aqua Ammonia  

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

component Removal in Flue Gas by Aqua Ammonia component Removal in Flue Gas by Aqua Ammonia Opportunity The Department of Energy's National Energy Technology Laboratory is seeking licensing partners interested in implementing United States Patent Number 7,255,842 entitled "Multi-component Removal in Flue Gas by Aqua Ammonia." This patent discloses a method for the removal of potential environmental-impacting compounds from flue gas streams. The method oxidizes some or all of the acid precursors such as sulfur dioxide (SO 2 ) and nitric oxides (NO x ) into sulfur trioxide and nitrogen dioxide, respectively. Following this step, the gas stream is then treated with aqua ammonia or ammonium hydroxide to capture the compounds via chemical absorption through acid-base or neutralization reactions where a fertilizer is formed.

113

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

114

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

115

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

116

DOE Removes Brookhaven Contractor  

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

DOE Removes DOE Removes Brookhaven Contractor Peña sends a message to DOE facilities nationwide INSIDE 2 Accelerator Rx 4 FermiKids 6 Spring at Fermilab Photos courtesy of Brookhaven National Laboratory by Judy Jackson, Office of Public Affairs Secretary of Energy Federico Peña announced on Thursday, May 1, that the Department of Energy would immediately terminate the current management contract with Associated Universities, Inc. at Brookhaven National Laboratory in Upton, New York. Peña said that he made the decision after receiving the results of a laboratory safety management review conducted by the independent oversight arm of DOE's Office of Environment, Safety and Health. In addition, the Secretary said he found unacceptable "the continued on page 8 Volume 20 Friday, May 16, 1997

117

Pneumatic soil removal tool  

DOE Patents (OSTI)

A soil removal tool is provided for removing radioactive soil, rock and other debris from the bottom of an excavation, while permitting the operator to be located outside of a containment for that excavation. The tool includes a fixed jaw, secured to one end of an elongate pipe, which cooperates with a movable jaw pivotably mounted on the pipe. Movement of the movable jaw is controlled by a pneumatic cylinder mounted on the pipe. The actuator rod of the pneumatic cylinder is connected to a collar which is slidably mounted on the pipe and forms part of the pivotable mounting assembly for the movable jaw. Air is supplied to the pneumatic cylinder through a handle connected to the pipe, under the control of an actuator valve mounted on the handle, to provide movement of the movable jaw.

Neuhaus, John E. (Newport News, VA)

1992-01-01T23:59:59.000Z

118

Pneumatic soil removal tool  

Science Conference Proceedings (OSTI)

A soil removal tool is provided for removing radioactive soil, rock and other debris from the bottom of an excavation, while permitting the operator to be located outside of a containment for that excavation. The tool includes a fixed jaw, secured to one end of an elongate pipe, which cooperates with a movable jaw pivotably mounted on the pipe. Movement of the movable jaw is controlled by a pneumatic cylinder mounted on the pipe. The actuator rod of the pneumatic cylinder is connected to a collar which is slidably mounted on the pipe and forms part of the pivotable mounting assembly for the movable jaw. Air is supplied to the pneumatic cylinder through a handle connected to the pipe, under the control of an actuator valve mounted on the handle, to provide movement of the movable jaw. 3 figs.

Neuhaus, J.E.

1992-10-13T23:59:59.000Z

119

IMPROVED PROCESSES TO REMOVE NAPHTHENIC ACIDS  

Science Conference Proceedings (OSTI)

In the second year of this project, we continued our effort to develop low temperature decarboxylation catalysts and investigate the behavior of these catalysts at different reaction conditions. We conducted a large number of dynamic measurements with crude oil and model compounds to obtain the information at different reaction stages, which was scheduled as the Task2 in our work plan. We developed a novel adsorption method to remove naphthenic acid from crude oil using naturally occurring materials such as clays. Our results show promise as an industrial application. The theoretical modeling proposed several possible reaction pathways and predicted the reactivity depending on the catalysts employed. From all of these studies, we obtained more comprehensive understanding about catalytic decarboxylation and oil upgrading based on the naphthenic acid removal concept.

Aihua Zhang; Qisheng Ma; Kangshi Wang, William A. Goddard, Yongchun Tang

2005-05-05T23:59:59.000Z

120

IMPROVED PROCESSES TO REMOVE NAPHTHENIC ACIDS  

SciTech Connect

In the first year of this project, we have established our experimental and theoretical methodologies for studies of the catalytic decarboxylation process. We have developed both glass and stainless steel micro batch type reactors for the fast screening of various catalysts with reaction substrates of model carboxylic acid compounds and crude oil samples. We also developed novel product analysis methods such as GC analyses for organic acids and gaseous products; and TAN measurements for crude oil. Our research revealed the effectiveness of several solid catalysts such as NA-Cat-1 and NA-Cat-2 for the catalytic decarboxylation of model compounds; and NA-Cat-5{approx}NA-Cat-9 for the acid removal from crude oil. Our theoretical calculations propose a three-step concerted oxidative decarboxylation mechanism for the NA-Cat-1 catalyst.

Aihua Zhang; Qisheng Ma; William A. Goddard; Yongchun Tang

2004-04-28T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Removal of plutonium and americium from alkaline waste solutions  

DOE Patents (OSTI)

High salt content, alkaline waste solutions containing plutonium and americium are contacted with a sodium titanate compound to effect removal of the plutonium and americium from the alkaline waste solution onto the sodium titanate and provide an effluent having a radiation level of less than 10 nCi per gram alpha emitters.

Schulz, Wallace W. (Richland, WA)

1979-01-01T23:59:59.000Z

122

Electrochemical assessment and service-life prediction of mechanically stabilized earth walls backfilled with crushed concrete and recycled asphalt pavement  

E-Print Network (OSTI)

A Mechanically Stabilized Earth (MSE) wall is a vertical grade separation that uses earth reinforcement extending laterally from the wall to take advantage of earth pressure to reduce the required design strength of the wall. MSE wall systems are often prefabricated to reduce construction time, thus improving constructability when compared with conventionally cast-in-place reinforced wall systems. However, there is a lack of knowledge for predicting the service-life of MSE retaining wall systems when recycled backfill materials such as Recycled Asphalt Pavement (RAP) and Crushed Concrete (CC) are used instead of Conventional Fill Material (CFM). The specific knowledge missing is how these recycled materials, when used as backfill in MSE wall systems, affects the corrosion rate of the reinforcing strips. This work addresses this knowledge gap by providing recommendations for MSE wall systems backfilled with CC or RAP, and provides a guide to predict the service-life based on corrosion rate test data obtained from embedding steel and galvanized-steel earth reinforcing strips embedded in MSE wall systems backfilled with CC, RAP, and CFM. Experimental data from samples emulating MSE wall systems with steel and galvanized-steel reinforcing strips embedded in CC and RAP were compared to samples with strips embedded in CFM. The results of the testing provide data and methodologies that may, depending on the environmental exposure conditions, justify the use of RAP and CC for the construction of MSE walls. If these backfill materials are obtained from the construction site, this could provide a significant cost savings during construction.

Esfeller, Michael Watts, Jr.

2006-08-01T23:59:59.000Z

123

Engine Removal Projection Tool  

DOE Green Energy (OSTI)

The US Navy has over 3500 gas turbine engines used throughout the surface fleet for propulsion and the generation of electrical power. Past data is used to forecast the number of engine removals for the next ten years and determine engine down times between removals. Currently this is done via a FORTRAN program created in the early 1970s. This paper presents results of R&D associated with creating a new algorithm and software program. We tested over 60 techniques on data spanning 20 years from over 3100 engines and 120 ships. Investigated techniques for the forecast basis including moving averages, empirical negative binomial, generalized linear models, Cox regression, and Kaplan Meier survival curves, most of which are documented in engineering, medical and scientific research literature. We applied those techniques to the data, and chose the best algorithm based on its performance on real-world data. The software uses the best algorithm in combination with user-friendly interfaces and intuitively understandable displays. The user can select a specific engine type, forecast time period, and op-tempo. Graphical displays and numerical tables present forecasts and uncertainty intervals. The technology developed for the project is applicable to other logistic forecasting challenges.

Ferryman, Thomas A.; Matzke, Brett D.; Wilson, John E.; Sharp, Julia L.; Greitzer, Frank L.

2005-06-02T23:59:59.000Z

124

Metal chelate process to remove pollutants from fluids  

DOE Patents (OSTI)

The present invention relates to improved methods using an organic iron chelate to remove pollutants from fluids, such as flue gas. Specifically, the present invention relates to a process to remove NO[sub x] and optionally SO[sub 2] from a fluid using a metal ion (Fe[sup 2+]) chelate wherein the ligand is a dimercapto compound wherein the --SH groups are attached to adjacent carbon atoms (HS--C--C--SH) or (SH--C--CCSH) and contain a polar functional group so that the ligand of DMC chelate is water soluble. Alternatively, the DMC is covalently attached to a water insoluble substrate such as a polymer or resin, e.g., polystyrene. The chelate is regenerated using electroreduction or a chemical additive. The dimercapto compound bonded to a water insoluble substrate is also useful to lower the concentration or remove hazardous metal ions from an aqueous solution. 26 figures.

Chang, S.G.T.

1994-12-06T23:59:59.000Z

125

Geothermal hydrogen sulfide removal  

DOE Green Energy (OSTI)

UOP Sulfox technology successfully removed 500 ppM hydrogen sulfide from simulated mixed phase geothermal waters. The Sulfox process involves air oxidation of hydrogen sulfide using a fixed catalyst bed. The catalyst activity remained stable throughout the life of the program. The product stream composition was selected by controlling pH; low pH favored elemental sulfur, while high pH favored water soluble sulfate and thiosulfate. Operation with liquid water present assured full catalytic activity. Dissolved salts reduced catalyst activity somewhat. Application of Sulfox technology to geothermal waters resulted in a straightforward process. There were no requirements for auxiliary processes such as a chemical plant. Application of the process to various types of geothermal waters is discussed and plans for a field test pilot plant and a schedule for commercialization are outlined.

Urban, P.

1981-04-01T23:59:59.000Z

126

Pneumatic soil removal tool  

Science Conference Proceedings (OSTI)

A soil tool is provided for removing radioactive soil, rock and debris from the bottom of an excavation, while permitting the operator to be located outside of a containment for that excavation. The tool includes a fixed jaw, secured to one end of an elongate pipe, which cooperates with a movable jaw pivotably mounted on the pipe. Movement of the movable jaw is controlled by a pneumatic cylinder on the pipe. The actuator rod of the pneumatic cylinder is connected to a collar which is slidably on the pipe and forms part of the pivotable mounting assembly for the movable jaw. Air is supplied to the pneumatic cylinder through a handle connected to the pipe, under the control of an actuator value mounted on the handle, to provide movement of the movable jaw.

Neuhaus, J.F.

1991-01-23T23:59:59.000Z

127

SOLAR HEATING OF TANK BOTTOMS Application of Solar Heating to Asphaltic and Parrafinic Oils Reducing Fuel Costs and Greenhouse Gases Due to Use of Natural Gas and Propane  

DOE Green Energy (OSTI)

The sale of crude oil requires that the crude meet product specifications for BS&W, temperature, pour point and API gravity. The physical characteristics of the crude such as pour point and viscosity effect the efficient loading, transport, and unloading of the crude oil. In many cases, the crude oil has either a very high paraffin content or asphalt content which will require either hot oiling or the addition of diluents to the crude oil to reduce the viscosity and the pour point of the oil allowing the crude oil to be readily loaded on to the transport. Marginal wells are significantly impacted by the cost of preheating the oil to an appropriate temperature to allow for ease of transport. Highly paraffinic and asphaltic oils exist throughout the D-J basin and generally require pretreatment during cold months prior to sales. The current study addresses the use of solar energy to heat tank bottoms and improves the overall efficiency and operational reliability of stripper wells.

Eugene A. Fritzler

2005-09-01T23:59:59.000Z

128

XAFS Model Compound Library  

DOE Data Explorer (OSTI)

The XAFS Model Compound Library contains XAFS data on model compounds. The term "model" compounds refers to compounds of homogeneous and well-known crystallographic or molecular structure. Each data file in this library has an associated atoms.inp file that can be converted to a feff.inp file using the program ATOMS. (See the related Searchable Atoms.inp Archive at http://cars9.uchicago.edu/~newville/adb/) This Library exists because XAFS data on model compounds is useful for several reasons, including comparing to unknown data for "fingerprinting" and testing calculations and analysis methods. The collection here is currently limited, but is growing. The focus to date has been on inorganic compounds and minerals of interest to the geochemical community. [Copied, with editing, from http://cars9.uchicago.edu/~newville/ModelLib/

Newville, Matthew

129

Preparation of uranium compounds  

SciTech Connect

UI.sub.3(1,4-dioxane).sub.1.5 and UI.sub.4(1,4-dioxane).sub.2, were synthesized in high yield by reacting turnings of elemental uranium with iodine dissolved in 1,4-dioxane under mild conditions. These molecular compounds of uranium are thermally stable and excellent precursor materials for synthesizing other molecular compounds of uranium including alkoxide, amide, organometallic, and halide compounds.

Kiplinger, Jaqueline L; Montreal, Marisa J; Thomson, Robert K; Cantat, Thibault; Travia, Nicholas E

2013-02-19T23:59:59.000Z

130

Process for preparing a chemical compound enriched in isotope content  

DOE Patents (OSTI)

A process to prepare a chemical enriched in isotope content which includes: (a) A chemical exchange reaction between a first and second compound which yields an isotopically enriched first compound and an isotopically depleted second compound; (b) the removal of a portion of the first compound as product and the removal of a portion of the second compound as spent material; (c) the conversion of the remainder of the first compound to the second compound for reflux at the product end of the chemical exchange reaction region; (d) the conversion of the remainder of the second compound to the first compound for reflux at the spent material end of the chemical exchange region; and the cycling of the additional chemicals produced by one conversion reaction to the other conversion reaction, for consumption therein. One of the conversion reactions is an oxidation reaction, and the energy that it yields is used to drive the other conversion reaction, a reduction. The reduction reaction is carried out in a solid polymer electrolyte electrolytic reactor. The overall process is energy efficient and yields no waste by-products.

Michaels, Edward D. (Spring Valley, OH)

1982-01-01T23:59:59.000Z

131

Partially fluorinated ionic compounds  

DOE Patents (OSTI)

Partially fluorinated ionic compounds are prepared. They are useful in the preparation of partially fluorinated dienes, in which the repeat units are cycloaliphatic.

Han, legal representative, Amy Qi (Hockessin, DE); Yang, Zhen-Yu (Hockessin, DE)

2008-11-25T23:59:59.000Z

132

Contributions to an Improved Oxygen and Thermal Transport Model and Development of Fatigue Analysis Software for Asphalt Pavements  

E-Print Network (OSTI)

Fatigue cracking is one primary distress in asphalt pavements, dominant especially in later years of service. Prediction of mixture fatigue resistance is critical for various applications, e.g., pavement design and preventative maintenance. The goal of this work was to develop a tool for prediction of binder aging level and mixture fatigue life in pavement from unaged binder/mixture properties. To fulfill this goal, binder oxidation during the early fast-rate period must be understood. In addition, a better hourly air temperature model is required to provide accurate input for the pavement temperature prediction model. Furthermore, a user-friendly software needs to be developed to incorporate these findings. Experiments were conducted to study the carbonyl group formation in one unmodified binder (SEM 64-22) and one polymer-modified binder (SEM 70-22), aged at five elevated temperatures. Data of SEM 64-22, especially at low temperatures, showed support for a parallel-reaction model, one first order reaction and one zero order reaction. The model did not fit data of SEM 70-22. The polymer modification of SEM 70-22 might be responsible for this discrepancy. Nonetheless, more data are required to draw a conclusion. Binder oxidation rate is highly temperature dependent. Hourly air temperature data are required as input for the pavement temperature prediction model. Herein a new pattern-based air temperature model was developed to estimate hourly data from daily data. The pattern is obtained from time series analysis of measured data. The new model yields consistently better results than the conventional sinusoidal model. The pavement aging and fatigue analysis (PAFA) software developed herein synthesizes new findings from this work and constant-rate binder oxidation and hardening kinetics and calibrated mechanistic approach with surface energy (CMSE) fatigue analysis algorithm from literature. Input data include reaction kinetics parameters, mixture test results, and pavement temperature. Carbonyl area growth, dynamic shear rheometer (DSR) function hardening, and mixture fatigue life decline are predicted as function of time. Results are plotted and saved in spreadsheets.

Jin, Xin

2009-08-01T23:59:59.000Z

133

Removal to Maximum Extent Practical  

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

Summary Notes from 1 November 2007 Generic Technical Issue Discussion on Removal of Highly Radioactive Radionuclides/Key Radionuclides to the Maximum Extent Practical

134

Method of and apparatus for removing silicon from a high temperature sodium coolant  

DOE Patents (OSTI)

A method of and system for removing silicon from a high temperature liquid sodium coolant system for a nuclear reactor. The sodium is cooled to a temperature below the silicon saturation temperature and retained at such reduced temperature while inducing high turbulence into the sodium flow for promoting precipitation of silicon compounds and ultimate separation of silicon compound particles from the liquid sodium.

Yunker, Wayne H. (Richland, WA); Christiansen, David W. (Kennewick, WA)

1987-01-01T23:59:59.000Z

135

Radioactive air emissions notice of construction fuel removal for 105-KE basin  

SciTech Connect

This document serves as a notice of construction (NOC), pursuant to the requirements of Washington Administrative Code (WAC) 246-247-060, and as a request for approval to construct pursuant to 40 Code of Federal Regulations (CFR) 61.96 for the modifications, installation of new equipment, and fuel removal and sludge relocation activities at 105-KE Basin. The 105-K east reactor and its associated spent nuclear fuel (SNF) storage basin (105-KE Basin) were constructed in the early 1950s and are located in the 100-K Area about 1,400 feet from the Columbia River. The 105-KE Basin contains 1,152 metric tons of SNF stored underwater in 3,673 open canisters. This SNF has been stored for varying periods of time ranging from 8 to 24 years. The 105-KE Basin is constructed of unlined concrete and contains approximately 1.3 million gallons of water with an asphaltic membrane beneath the pool. The fuel is corroding and an estimated 1,700 cubic feet of sludge, containing radionuclides and miscellaneous materials, have accumulated in the basin. The 105-KE Basin has leaked radiologically contaminated water to the soil beneath the basin in the past most likely at the construction joint between the foundation of the basin and the foundation of the reactor. The purpose of the activities described in this Notice of Construction (NOC) is to enable the retrieval and transport of the fuel to the Cold Vacuum Drying Facility (CVDF). This NOC describes modifications, the installation of new equipment, and fuel removal and sludge relocation activities expected to be routine in the future. Debris removal activities described in this NOC will supersede the previously approved NOC (DOE/RL-95-65). The proposed modifications described are scheduled to begin in calendar year 1997.

Kamberg, L.D., Fluor Daniel Hanford

1997-02-11T23:59:59.000Z

136

CRBRP decay heat removal systems  

SciTech Connect

The Decay Heat Removal Systems for the Clinch River Breeder Reactor Plant (CRBRP) are designed to adequately remove sensible and decay heat from the reactor following normal shutdown, operational occurrences, and postulated accidents on both a short term and a long term basis. The Decay Heat Removal Systems are composed of the Main Heat Transport System, the Main Condenser and Feedwater System, the Steam Generator Auxiliary Heat Removal System (SGAHRS), and the Direct Heat Removal Service (DHRS). The overall design of the CRBRP Decay Heat Removal Systems and the operation under normal and off-normal conditions is examined. The redundancies of the system design, such as the four decay heat removal paths, the emergency diesel power supplies, and the auxiliary feedwater pumps, and the diversities of the design such as forced circulation/natural circulation and AC Power/DC Power are presented. In addition to overall design and system capabilities, the detailed designs for the Protected Air Cooled Condensers (PACC) and the Air Blast Heat Exchangers (ABHX) are presented.

Hottel, R.E.; Louison, R.; Boardman, C.E.; Kiley, M.J.

1977-01-01T23:59:59.000Z

137

Heart testing compound  

DOE Patents (OSTI)

The compound 15-(p-(/sup 125/I)-iodophenyl)-6-tellurapentadecanoic acid is disclosed as a myocardial imaging agent having rapid and pronounced uptake, prolonged myocardial retention, and low in vivo deiodination.

Knapp, F.F. Jr.; Goodman, M.M.

1983-06-29T23:59:59.000Z

138

Heart testing compound  

DOE Patents (OSTI)

The compound 15-(p-[.sup.125 I]-iodophenyl)-6-tellurapentadecanoic acid is disclosed as a myocardial imaging agent having rapid and pronounced uptake, prolonged myocardial retention, and low in vivo deiodination.

Knapp, Jr., Furn F. (Oak Ridge, TN); Goodman, Mark M. (Knoxville, TN)

1985-01-01T23:59:59.000Z

139

Nitrogen Removal From Low Quality Natural Gas  

SciTech Connect

Natural gas provides more than one-fifth of all the primary energy used in the United States. It is especially important in the residential sector, where it supplies nearly half of all the energy consumed in U.S. homes. However, significant quantities of natural gas cannot be produced economically because its quality is too low to enter the pipeline transportation system without some type of processing, other than dehydration, to remove the undesired gas fraction. Such low-quality natural gas (LQNG) contains significant concentration or quantities of gas other than methane. These non- hydrocarbons are predominantly nitrogen, carbon dioxide, and hydrogen sulfide, but may also include other gaseous components. The nitrogen concentrations usually exceeds 4%. Nitrogen rejection is presently an expensive operation which can present uneconomic scenarios in the potential development of natural gas fields containing high nitrogen concentrations. The most reliable and widely used process for nitrogen rejection from natural gas consists of liquefying the feed stream using temperatures in the order of - 300{degrees}F and separating the nitrogen via fractionation. In order to reduce the gas temperature to this level, the gas is compressed, cooled by mullet-stream heat exchangers, and expanded to low pressure. Significant energy for compression and expensive materials of construction are required. Water and carbon dioxide concentrations must be reduced to levels required to prevent freezing. SRI`s proposed research involves screening new nitrogen selective absorbents and developing a more cost effective nitrogen removal process from natural gas using those compounds. The long-term objective of this project is to determine the technical and economical feasibility of a N{sub 2}2 removal concept based on complexation of molecular N{sub 2} with novel complexing agents. Successful development of a selective, reversible, and stable reagent with an appropriate combination of capacity and N{sub 2} absorption/desorption characteristics will allow selective separation of N{sub 2} from LQNG.

Alvarado, D.B.; Asaro, M.F.; Bomben, J.L.; Damle, A.S.; Bhown, A.S.

1997-10-01T23:59:59.000Z

140

Electrospun Polyurethane Fibers for Absorption of Volatile Organic Compounds from Air  

E-Print Network (OSTI)

Electrospun polyurethane fibers for removal of volatile organic compounds (VOC) from air with rapid VOC absorption and desorption have been developed. Polyurethanes based on 4,4-methylenebis(phenylisocyanate) (MDI) and ...

Scholten, Elke

Note: This page contains sample records for the topic "removing asphalt compounds" 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
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141

Article removal device for glovebox  

DOE Patents (OSTI)

An article removal device for a glovebox is described comprising a conduit extending through a glovebox wall which may be closed by a plug within the glovebox, and a fire-resistant container closing the outer end of the conduit and housing a removable container for receiving pyrophoric or otherwise hazardous material without disturbing the interior environment of the glovebox or adversely affecting the environment outside of the glovebox. (Official Gazette)

Guyer, R.H.; Leebl, R.G.

1973-12-01T23:59:59.000Z

142

Method of upgrading oils containing hydroxyaromatic hydrocarbon compounds to highly aromatic gasoline  

DOE Patents (OSTI)

The present invention is a multi-stepped method of converting an oil which is produced by various biomass and coal conversion processes and contains primarily single and multiple ring hydroxyaromatic hydrocarbon compounds to highly aromatic gasoline. The single and multiple ring hydroxyaromatic hydrocarbon compounds in a raw oil material are first deoxygenated to produce a deoxygenated oil material containing single and multiple ring aromatic compounds. Then, water is removed from the deoxygenated oil material. The next step is distillation to remove the single ring aromatic compounds as gasoline. In the third step, the multiple ring aromatics remaining in the deoxygenated oil material are cracked in the presence of hydrogen to produce a cracked oil material containing single ring aromatic compounds. Finally, the cracked oil material is then distilled to remove the single ring aromatics as gasoline.

Baker, E.G.; Elliott, D.C.

1993-01-19T23:59:59.000Z

143

Charge Density Wave Compounds  

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

Fisher Research Group Fisher Research Group Layered Chalcogenides 29 February 2008 Controlling the Wave by Brad Plummer, SLAC Communications Stanford University researchers working in part at SSRL have discovered a novel set of properties pertaining to a compound of materials called tritellurides. These compounds, composed of three atoms of tellurium and a single atom of one of the rare earth elements, demonstrate unique electronic properties that can be controlled by altering the temperature of the material. The tritellurides display phenomena known as charge density waves (CDW). In a normal conductive metal, electrons persist in a "sea" wherein they are evenly distributed and equally available, or conductive. A CDW occurs under certain circumstances and causes the electrons to clump together, lowering their availability, and thereby lowering the compound's conductivity. Tellurium, when crystallized into quasi-two-dimensional planes and combined with rare earth elements, produces a material with CDWs that can be manipulated and controlled.

144

Stable surface passivation process for compound semiconductors  

DOE Patents (OSTI)

A passivation process for a previously sulfided, selenided or tellurated III-V compound semiconductor surface. The concentration of undesired mid-gap surface states on a compound semiconductor surface is reduced by the formation of a near-monolayer of metal-(sulfur and/or selenium and/or tellurium)-semiconductor that is effective for long term passivation of the underlying semiconductor surface. Starting with the III-V compound semiconductor surface, any oxidation present thereon is substantially removed and the surface is then treated with sulfur, selenium or tellurium to form a near-monolayer of chalcogen-semiconductor of the surface in an oxygen-free atmosphere. This chalcogenated surface is then contacted with a solution of a metal that will form a low solubility chalcogenide to form a near-monolayer of metal-chalcogen-semiconductor. The resulting passivating layer provides long term protection for the underlying surface at or above the level achieved by a freshly chalcogenated compound semiconductor surface in an oxygen free atmosphere.

Ashby, Carol I. H. (Edgewood, NM)

2001-01-01T23:59:59.000Z

145

High removal rate laser-based coating removal system  

DOE Patents (OSTI)

A compact laser system that removes surface coatings (such as paint, dirt, etc.) at a removal rate as high as 1000 ft.sup.2 /hr or more without damaging the surface. A high repetition rate laser with multiple amplification passes propagating through at least one optical amplifier is used, along with a delivery system consisting of a telescoping and articulating tube which also contains an evacuation system for simultaneously sweeping up the debris produced in the process. The amplified beam can be converted to an output beam by passively switching the polarization of at least one amplified beam. The system also has a personal safety system which protects against accidental exposures.

Matthews, Dennis L. (Moss Beach, CA); Celliers, Peter M. (Berkeley, CA); Hackel, Lloyd (Livermore, CA); Da Silva, Luiz B. (Danville, CA); Dane, C. Brent (Livermore, CA); Mrowka, Stanley (Richmond, CA)

1999-11-16T23:59:59.000Z

146

Removal - An alternative to clearance  

SciTech Connect

This presentation shows the differences between the application of clearance and removal, both being procedures for materials leaving radiation protection areas permanently. The differentiation will be done on the basis of the German legislation but may be also applicable for other national legislation. For clearance in Germany two basic requirements must be given, i.e. that the materials are activated or contaminated and that they result from the licensed use or can be assigned to the scope of the license. Clearance needs not to be applied to objects in Germany which are to be removed only temporarily from controlled areas with the purpose of repair or reuse in other controlled areas. In these cases only the requirements of contamination control apply. In the case of removal it must either be proved by measurements that the relevant materials are neither activated nor contaminated or that the materials result from areas where activation or contamination is impossible due to the operational history considering operational procedures and events. If the material is considered neither activated nor contaminated there is no need for a clearance procedure. Therefore, these materials can be removed from radiation protection areas and the removal is in the responsibility of the licensee. Nevertheless, the removal procedure and the measuring techniques to be applied for the different types of materials need an agreement from the competent authority. In Germany a maximum value of 10% of the clearance values has been established in different licenses as a criterion for the application of removal. As approximately 2/3 of the total mass of a nuclear power plant is not expected to be contaminated or activated there is a need for such a procedure of removal for this non contaminated material without any regulatory control especially in the case of decommissioning. A remarkable example is NPP Stade where in the last three years more than 8600 Mg were disposed of by removal and only 315 Mg were released by clearance, even before the decommissioning licensing procedure was finished. (authors)

Feinhals, J.; Kelch, A. [TUV NORD SysTec GmbH and Co. KG, Hamburg (Germany); Kunze, V. [Federal Office for Radiation Protection, Salzgitter (Germany)

2007-07-01T23:59:59.000Z

147

Large Component Removal/Disposal  

Science Conference Proceedings (OSTI)

This paper describes the removal and disposal of the large components from Maine Yankee Atomic Power Plant. The large components discussed include the three steam generators, pressurizer, and reactor pressure vessel. Two separate Exemption Requests, which included radiological characterizations, shielding evaluations, structural evaluations and transportation plans, were prepared and issued to the DOT for approval to ship these components; the first was for the three steam generators and one pressurizer, the second was for the reactor pressure vessel. Both Exemption Requests were submitted to the DOT in November 1999. The DOT approved the Exemption Requests in May and July of 2000, respectively. The steam generators and pressurizer have been removed from Maine Yankee and shipped to the processing facility. They were removed from Maine Yankee's Containment Building, loaded onto specially designed skid assemblies, transported onto two separate barges, tied down to the barges, th en shipped 2750 miles to Memphis, Tennessee for processing. The Reactor Pressure Vessel Removal Project is currently under way and scheduled to be completed by Fall of 2002. The planning, preparation and removal of these large components has required extensive efforts in planning and implementation on the part of all parties involved.

Wheeler, D. M.

2002-02-27T23:59:59.000Z

148

Multipollutant Removal with WOWClean® System  

E-Print Network (OSTI)

WOW Energy built and tested its multipollutant removal WOWClean® system in a development program with the Texas Commission on Environmental Quality (TCEQ). A 2,500 ACFM mobile unit was built to field test the removal of air pollution constituents from the flue gas of a power plant and demonstrate the technology. The system integrates proven emission reduction techniques into a single, multi-pollutant reduction system and is designed to remove Mercury, SOx, NOx, particulates, heavy metals and other pollutants from low temperature flue gases. Its advantages include robust operation, lower investment, lower operating cost and high removal rates. The WOWClean® system has been tested on flue gases resulting from the combustion of diverse fuels such as petcoke, coal, wood, diesel and natural gas. In addition to significant removal of CO2, test results demonstrate the capability to reduce 99.5% SOx (from levels as high as 2200 ppm), 90% reduction of NOx, and > 90% heavy metals. The paper will include details of the multi-pollutant system along with test results.

Romero, M.

2010-01-01T23:59:59.000Z

149

Vietnam HEU Removal | National Nuclear Security Administration  

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

Removal NNSANews posted a photo: Vietnam HEU Removal A truck carrying the last highly enriched uranium in Vietnam winds through the Vietnamese countryside. Facebook Twitter Youtube...

150

8-fluoropurine compounds  

DOE Patents (OSTI)

An efficient, regiocontrolled approach to the synthesis of 8-fluoropurines by direct fluorination of purines with dilute elemental fluorine, or acetyl hypofluorite, is provided. In a preferred embodiment, a purine compound is dissolved in a polar solvent and reacted with a dilute mixture of F.sub.2 in He or other inert gas.

Barrio, Jorge R. (Agoura Hills, CA); Satyamurthy, Nagichettiar (Los Angeles, CA); Namavari, Mohammad (Los Angeles, CA); Phelps, Michael E. (Encino, CA)

2001-01-01T23:59:59.000Z

151

Compound semiconductor MOSFETs  

Science Conference Proceedings (OSTI)

Enhancement mode, high electron mobility MOSFET devices have been fabricated using an oxide high-@k gate dielectric stack developed using molecular beam epitaxy. A template layer of Ga"2O"3, initially deposited on the surface of the III-V device unpins ... Keywords: Compound semiconductors, GaAs gate dielectric, III-V MOSFETs

R. Droopad; K. Rajagopalan; J. Abrokwah; P. Zurcher; M. Passlack

2007-09-01T23:59:59.000Z

152

A compound parabolic concentrator  

SciTech Connect

A compound parabolic concentrator (CPC) for solar energy applications is presented in this work. A prototype was built and its thermal performance was determined. Operating temperatures of the order of 150 /sup 0/C with a reasonable efficiency can be attained by means of a fixed CPC.

Manrique, J.A.

1984-05-01T23:59:59.000Z

153

Field sampling and analysis plan for the removal action at the former YS-860 Firing Ranges, Oak Ridge Y-12 Plant, Oak Ridge, Tennessee  

Science Conference Proceedings (OSTI)

The former YS-860 Firing Ranges are located at the eastern end of the Oak Ridge Y-12 Plant outside the primary facility fence line and west of Scarboro Road within the Upper East Fork Poplar Creek watershed in Oak Ridge, Tennessee. A decision has been made by the US Department of Energy to conduct a removal action of lead-contaminated soils at this site as part of early source actions within the Upper East Fork Poplar Creek watershed. This non-time critical removal action of bullets and lead-contaminated soil from the YS-860 Firing Ranges is being conducted as a Comprehensive Environmental Response, Compensation, and Liability Act of 1980 action. These actions are consistent with the Oak Ridge Reservation Environmental Restoration Program. The removal action will focus on the excavation of bullets and lead-contaminated soil from the shooting range berms, transportation of the material to a permitted treatment facility for disposal, demolition and land filling of a concrete trench and asphalt pathways at the site, and grading and revegetating of the entire site. This report is the field sampling and analysis plan for the removal action at the former YS-860 Firing Ranges. The field sampling and analysis plan addresses environmental sampling for lead after the removal of lead-contaminated soil from the target berm area. The objective of this sampling plan is to obtain sufficient analytical data to confirm that the removal action excavation has successfully reduced lead levels in soil to below the action level of 1,400 micrograms/g.

NONE

1998-03-01T23:59:59.000Z

154

Metals removal from spent salts  

DOE Patents (OSTI)

A method and apparatus for removing metal contaminants from the spent salt of a molten salt oxidation (MSO) reactor is described. Spent salt is removed from the reactor and analyzed to determine the contaminants present and the carbonate concentration. The salt is dissolved in water, and one or more reagents may be added to precipitate the metal oxide and/or the metal as either metal oxide, metal hydroxide, or as a salt. The precipitated materials are filtered, dried and packaged for disposal as waste or can be immobilized as ceramic pellets. More than about 90% of the metals and mineral residues (ashes) present are removed by filtration. After filtration, salt solutions having a carbonate concentration >20% can be spray-dried and returned to the reactor for re-use. Salt solutions containing a carbonate concentration <20% require further clean-up using an ion exchange column, which yields salt solutions that contain less than 1.0 ppm of contaminants.

Hsu, Peter C. (Pleasanton, CA); Von Holtz, Erica H. (Livermore, CA); Hipple, David L. (Livermore, CA); Summers, Leslie J. (Livermore, CA); Brummond, William A. (Livermore, CA); Adamson, Martyn G. (Danville, CA)

2002-01-01T23:59:59.000Z

155

Actinide removal from spent salts  

DOE Patents (OSTI)

A method for removing actinide contaminants (uranium and thorium) from the spent salt of a molten salt oxidation (MSO) reactor is described. Spent salt is removed from the reactor and analyzed to determine the contaminants present and the carbonate concentration. The salt is dissolved in water, and one or more reagents are added to precipitate the thorium as thorium oxide and/or the uranium as either uranium oxide or as a diuranate salt. The precipitated materials are filtered, dried and packaged for disposal as radioactive waste. About 90% of the thorium and/or uranium present is removed by filtration. After filtration, salt solutions having a carbonate concentration >20% can be dried and returned to the reactor for re-use. Salt solutions containing a carbonate concentration <20% require further clean-up using an ion exchange column, which yields salt solutions that contain less than 0.1 ppm of thorium or uranium.

Hsu, Peter C. (Pleasanton, CA); von Holtz, Erica H. (Livermore, CA); Hipple, David L. (Livermore, CA); Summers, Leslie J. (Livermore, CA); Adamson, Martyn G. (Danville, CA)

2002-01-01T23:59:59.000Z

156

Characterization of nickel and vanadium compounds in tar sand bitumen by UV-VIS spectroscopy and size exclusion chromatography coupled with element specific detection  

Science Conference Proceedings (OSTI)

Previously, the authors examined the Ni and V in heavy crude oils, residua, and processed products by several metal speciation techniques to ascertain molecular structure and processing behavior. Two classes of metal compounds were found - metallopetroporphyrins and metallo-nonprophyrins - each having unique reactivity during processing. In efforts to better understand the binding of metals in the oil medium, they now examine NI and V in tar sand bitumens. The bitumen was solvent extracted from the sand matrix and was separated by column chromatography and the petroporphyrin content was quantitated by UV-vis spectroscopy. The petroporphyrin contents ranged from virtually none to over 36% of the total metals. Asphalt Ridge (Utah) has primarily Ni petroporphyrins; Big Clifty (Kentucky) and Athabasca (Canada) have primarily V petroporphyrins; Arroyo Grande and McKittrick (California) have roughly equal amounts of both types; and Sunnyside (Utah) has virtually none of either.

Reynolds, J.G.; Jones, E.L.; Bennett, J.A. (Lawrence Livermore National Lab., CA (USA)); Biggs, W.R. (Chevron Research Co., Richmond, CA (USA))

1989-01-01T23:59:59.000Z

157

Development of statistical wet weather model to evaluate frictional properties at the pavement-tire interface on hot mix asphalt concrete  

E-Print Network (OSTI)

Skid resistance on wet pavements is influenced by friction at the tire-pavement interface as well as overall hot mix asphalt (HMA) performance. It is important to control aggregate, asphalt, and mix properties to achieve desirable frictional properties on HMA during its service life. Aggregate consensus and source properties influence frictional properties at the surface as well as aggregate matrix properties that affect overall skid performance. Thus, it is important to identify and control these properties through an effective testing and monitoring program. Research studies have indicated that current testing protocol for pre-qualification of aggregates being used by DOT's is tenuous and needs definitive evaluation. The validity of some tests currently being used for pre-qualification of aggregates is being questioned due to poor field correlation. Thus, there is a need for upgrading current testing criteria and aggregate classification system in view of new techniques that can be used either as replacements and/or supplements to current tests. This study, a part of the Texas Department of Transportation (TxDOT) current research program to evaluate inadequacies of current tests to skid performance, focuses on tests evaluating aggregate shape and distribution parameters. In this study, a wet weather test selection criteria was developed to evaluate the effectiveness of current and new testing techniques to monitor aggregate shape, texture, and distribution characteristics. Extensive tests were conducted on forty aggregates selected from TxDOT Quality Material Catalogue covering various parts of U.S.A. Fine aggregates tests including the Uncompacted Void Content, the Compacted Aggregate Resistance, the Methylene Blue, and the Particle Size Analysis were performed to evaluate angularity, texture, and distribution characteristics within fine aggregates. Flat and elongated tests on coarse aggregates were also performed using both conventional and automated techniques to analyze shape and size distribution characteristics. A statistical analysis was performed to select tests that would enable monitoring of aggregate shape and distribution properties enhancing skid performance. The evaluation criteria were based upon a sensitivity and correlation analysis to evaluate consistency, reproducibility, and ability of tests to effectively discern aggregates with good and marginal performance.

Bedi, Harpreet

2001-01-01T23:59:59.000Z

158

Hydrogen in compound semiconductors  

DOE Green Energy (OSTI)

Progress in the understanding of hydrogen and its interactions in III/V and II/VI compound semiconductors is reviewed. Donor, acceptor and deep level passivation is well established in III/V compounds based on electrical measurements and on spectroscopic studies. The hydrogen donor levels in GaAs and GaP are estimated to lie near E{sub v}+0.5 eV and E{sub v}+0.3 eV, respectively. Arsenic acceptors have been passivated by hydrogen in CdTe and the very first nitrogen-hydrogen local vibrational model spectra in ZnSe have been reported. This long awaited result may lead to an explanation for the poor activation of nitrogen acceptors in ZnSe grown by techniques which involve high concentrations of hydrogen.

Haller, E.E.

1993-05-01T23:59:59.000Z

159

Forecast Technical Document Felling and Removals  

E-Print Network (OSTI)

Forecast Technical Document Felling and Removals Forecasts A document describing how volume fellings and removals are handled in the 2011 Production Forecast system. Tom Jenkins Robert Matthews Ewan Mackie Lesley Halsall #12;PF2011 ­ Felling and removals forecasts Background A fellings and removals

160

Injection Molding Compounds  

Science Conference Proceedings (OSTI)

Table 5   Common thermoplastic and thermoset molding compounds...(r) (s) (t) Phenolic Distributor caps, plastic ash trays (a) (b) (g) (h) (i) (j) (k) (l) (m) (n) (o) (q) (r) (s) (t) Urethane Automotive body panels, bumpers (a) (d) (e) (g) (i) (l) (m) (o) (q) (r) (t) Vinyl ester Composite car/truck springs, wheels (b) (d) (e) (g) (i) (j) (k) (l) (m) (n) (o) (p)...

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161

High removal rate laser-based coating removal system  

Science Conference Proceedings (OSTI)

A compact laser system is disclosed that removes surface coatings (such as paint, dirt, etc.) at a removal rate as high as 1,000 ft{sup 2}/hr or more without damaging the surface. A high repetition rate laser with multiple amplification passes propagating through at least one optical amplifier is used, along with a delivery system consisting of a telescoping and articulating tube which also contains an evacuation system for simultaneously sweeping up the debris produced in the process. The amplified beam can be converted to an output beam by passively switching the polarization of at least one amplified beam. The system also has a personal safety system which protects against accidental exposures.

Matthews, D.L.; Celliers, P.M.; Hackel, L.; Da Silva, L.B.; Dane, C.B.; Mrowka, S.

1999-11-16T23:59:59.000Z

162

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

163

Method of upgrading oils containing hydroxyaromatic hydrocarbon compounds to highly aromatic gasoline  

DOE Patents (OSTI)

The present invention is a multi-stepped method of converting an oil which is produced by various biomass and coal conversion processes and contains primarily single and multiple ring hydroxyaromatic hydrocarbon compounds to highly aromatic gasoline. The single and multiple ring hydroxyaromatic hydrocarbon compounds in a raw oil material are first deoxygenated to produce a deoxygenated oil material containing single and multiple ring aromatic compounds. Then, water is removed from the deoxygenated oil material. The next step is distillation to remove the single ring aromatic compouns as gasoline. In the third step, the multiple ring aromatics remaining in the deoxygenated oil material are cracked in the presence of hydrogen to produce a cracked oil material containing single ring aromatic compounds. Finally, the cracked oil material is then distilled to remove the single ring aromatics as gasoline.

Baker, Eddie G. (Richland, WA); Elliott, Douglas C. (Richland, WA)

1993-01-01T23:59:59.000Z

164

Method of and apparatus for removing silicon from a high temperature sodium coolant  

DOE Patents (OSTI)

This patent discloses a method of and system for removing silicon from a high temperature liquid sodium coolant system for a nuclear reactor. The sodium is cooled to a temperature below the silicon saturation temperature and retained at such reduced temperature while inducing high turbulence into the sodium flow for promoting precipitation of silicon compounds and ultimate separation of silicon compound particles from the liquid sodium.

Yunker, W.H.; Christiansen, D.W.

1983-11-25T23:59:59.000Z

165

Polymer formulation for removing hydrogen and liquid water from an enclosed space  

DOE Patents (OSTI)

This invention describes a solution to the particular problem of liquid water formation in hydrogen getters exposed to quantities of oxygen. Water formation is usually desired because the recombination reaction removes hydrogen without affecting gettering capacity and the oxygen removal reduces the chances for a hydrogen explosion once free oxygen is essentially removed. The present invention describes a getter incorporating a polyacrylate compound that can absorb up to 500% of its own weight in liquid water without significantly affecting its hydrogen gettering/recombination properties, but that also is insensitive to water vapor.

Shepodd, Timothy J. (Livermore, CA)

2006-02-21T23:59:59.000Z

166

Chloride removal from plutonium alloy  

Science Conference Proceedings (OSTI)

SRP is evaluating a program to recover plutonium from a metallic alloy that will contain chloride salt impurities. Removal of chloride to sufficiently low levels to prevent damaging corrosion to canyon equipment is feasible as a head-end step following dissolution. Silver nitrate and mercurous nitrate were each successfully used in laboratory tests to remove chloride from simulated alloy dissolver solution containing plutonium. Levels less than 10 ppM chloride were achieved in the supernates over the precipitated and centrifuged insoluble salts. Also, less than 0.05% loss of plutonium in the +3, +4, or +6 oxidation states was incurred via precipitate carrying. These results provide impetus for further study and development of a plant-scale process to recover plutonium from metal alloy at SRP.

Holcomb, H.P.

1983-01-01T23:59:59.000Z

167

Improved Processes to Remove Naphthenic Acids  

Science Conference Proceedings (OSTI)

In the past three years, we followed the work plan as we suggested in the proposal and made every efforts to fulfill the project objectives. Based on our large amount of creative and productive work, including both of experimental and theoretic aspects, we received important technical breakthrough on naphthenic acid removal process and obtained deep insight on catalytic decarboxylation chemistry. In detail, we established an integrated methodology to serve for all of the experimental and theoretical work. Our experimental investigation results in discovery of four type effective catalysts to the reaction of decarboxylation of model carboxylic acid compounds. The adsorption experiment revealed the effectiveness of several solid materials to naphthenic acid adsorption and acidity reduction of crude oil, which can be either natural minerals or synthesized materials. The test with crude oil also received promising results, which can be potentially developed into a practical process for oil industry. The theoretical work predicted several possible catalytic decarboxylation mechanisms that would govern the decarboxylation pathways depending on the type of catalysts being used. The calculation for reaction activation energy was in good agreement with our experimental measurements.

Aihua Zhang; Qisheng Ma; Kangshi Wang; Yongchun Tang; William A. Goddard

2005-12-09T23:59:59.000Z

168

Removing Barriers to Interdisciplinary Research  

E-Print Network (OSTI)

A significant amount of high-impact contemporary scientific research occurs where biology, computer science, engineering and chemistry converge. Although programmes have been put in place to support such work, the complex dynamics of interdisciplinarity are still poorly understood. In this paper we interrogate the nature of interdisciplinary research and how we might measure its "success", identify potential barriers to its implementation, and suggest possible mechanisms for removing these impediments.

Naomi Jacobs; Martyn Amos

2010-12-19T23:59:59.000Z

169

METHOD OF REMOVING STRONTIUM IONS  

DOE Patents (OSTI)

A method is given for removing trace amounts of Sr/sup 90/ from solutions. Phosphate ion is added to the solution and it is then brought into contact with a solid salt such as calcium carbonate which will react methathetically with the phosphate ion to form a salt such as calcium phosphate. During this reaction, strontium will be absorbed to a high degree within the newly formed lattice. (AEC)

Rhodes, D.W.; McHenry, J.R.; Ames, L.L. Jr.

1962-05-01T23:59:59.000Z

170

Mercury removal in utility wet scrubber using a chelating agent  

DOE Patents (OSTI)

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

Amrhein, Gerald T. (Louisville, OH)

2001-01-01T23:59:59.000Z

171

Radioactive air emissions notice of construction fuel removal for 105-KW Basin  

Science Conference Proceedings (OSTI)

This document serves as a Notice of Construction (NOC), pursuant to the requirements of Washington Administrative Code (WAC) 246-247-060, and as a request for approval to construct, pursuant to 40 Code of Federal Regulations (CFR) 61.96, for the modifications, installation of new equipment, and fuel removal and sludge relocation activities at 105-KW Basin. The purpose of the activities described in this NOC is to enable the eventual retrieval and transport of the fuel for processing. The fuel retrieval and transport will require an integrated water treatment system for which performance specifications have been developed. These specifications are currently in the procurement process. Following procurement (and before installation of this system and the handling of fuel) design details will be provided to Washington State Department of Health (WDOH). The 105-K West Reactor (105-KW) and its associated spent nuclear fuel (SNF) storage basin were constructed in the early 1950s and are located on the Hanford Site in the 100-K Area about 1,400 feet from the Columbia River. The 105-KW Basin contains 964 Metric Tons of SNF stored under water in approximately 3,800 closed canisters. This SNF has been stored for varying periods of time ranging from 8 to 17 years. The 105-KW Basin is constructed of concrete with an epoxy coating and contains approximately 1.3 million gallons of water with an asphaltic membrane beneath the pool. Although the 105-KW Basin has not been known to leak, the discharge chute and associated construction joint have been isolated from the rest of the basin by metal isolation barriers. This was a precautionary measure, to mitigate the consequences of a seismic event. The proposed modifications described are scheduled to begin in calendar year 1997.

Hays, C.B.

1997-05-29T23:59:59.000Z

172

Feed gas contaminant removal in ion transport membrane systems  

DOE Patents (OSTI)

An oxygen ion transport membrane process wherein a heated oxygen-containing gas having one or more contaminants is contacted with a reactive solid material to remove the one or more contaminants. The reactive solid material is provided as a deposit on a support. The one or more contaminant compounds in the heated oxygen-containing gas react with the reactive solid material. The contaminant-depleted oxygen-containing gas is contacted with a membrane, and oxygen is transported through the membrane to provide transported oxygen.

Underwood, Richard Paul (Allentown, PA); Makitka, III, Alexander (Hatfield, PA); Carolan, Michael Francis (Allentown, PA)

2012-04-03T23:59:59.000Z

173

Natural gas: Removing the obstacles  

Science Conference Proceedings (OSTI)

Defining and then figuring out how to remove whatever obstacles may be blocking the wider use of natural gas was the purpose of a conference held early last month in Phoenix, Arizona. The unique, three-day event was jointly sponsored by the U.S. Department of Energy (DOE) and the National Association of Regulatory Utility Commissioners (NARUC). It drew an overflow crowd of more than 500, with a registration list that read like a Who's Who of the natural gas industry. This article summarizes some of the main points of this conference.

Romo, C.

1992-03-15T23:59:59.000Z

174

Role of fly ash in the removal of organic pollutants from wastewater  

Science Conference Proceedings (OSTI)

Fly ash, a relatively abundant and inexpensive material, is currently being investigated as an adsorbent for the removal of various organic pollutants from wastewater. The wastewater contains various types of phenolic compounds, such as chloro, nitro, amino, and other substituted compounds. Various types of pesticides, such as lindane, malathion, carbofuran, etc., and dyes, such as, methylene blue, crystal violet, malachite green, etc., are also present in the wastewater. These contaminants pollute the water stream. These organic pollutants, such as phenolic compounds, pesticides, and dyes, etc., can be removed very effectively using fly ash as adsorbent. This article presents a detailed review on the role of fly ash in the removal of organic pollutants from wastewater. Adsorption of various pollutants using fly ash has been reviewed. The adsorption mechanism and other influencing factors, favorable conditions, and competitive ions, etc., on the adsorption process have also been discussed in this paper. It is evident from the review that fly ash has demonstrated good removal capabilities for various organic compounds. 171 refs., 3 figs., 5 tabs.

M. Ahmaruzzaman [National Institute of Technology, Silchar (India). Department of Chemistry

2009-03-15T23:59:59.000Z

175

Material Removal and Disposition | National Nuclear Security...  

National Nuclear Security Administration (NNSA)

Removal and Disposition | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response...

176

Sandia National Labs: PCNSC: Research: Compound Semiconductor...  

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

Compound Semiconductor Science and Technology Thrust The Physical, Chemical, and Nano Sciences Center's vision for Compound Semiconductors is to develop the science of compound...

177

Process for preparing a chemical compound enriched in isotope content. [nitrogen 15-enriched nitric acid  

DOE Patents (OSTI)

A process to prepare a chemical enriched in isotope content includes: a chemical exchange reaction between a first and second compound which yields an isotopically enriched first compound and an isotopically depleted second compound; the removal of a portion of the first compound as product and the removal of a portion of the second compound as spent material; the conversion of the remainder of the first compound to the second compound for reflux at the product end of the chemical exchange reaction region; the conversion of the remainder of the second compound to the first compound for reflux at the spent material end of the chemical exchange region; and the cycling of the additional chemicals produced by one conversion reaction to the other conversion reaction, for consumption therein. One of the conversion reactions is an oxidation reaction, and the energy that it yields is used to drive the other conversion reaction, a reduction. The reduction reaction is carried out in a solid polymer electrolyte electrolytic reactor. The overall process is energy efficient and yields no waste by-products. A particular embodiment of the process in the production of nitrogen-15-enriched nitric acid.

Michaels, E.D.

1981-02-25T23:59:59.000Z

178

Regenerable Sorbent Development for Sulfur, Chloride and Ammonia Removal from Coal-Derived Synthesis Gas  

DOE Green Energy (OSTI)

A large number of components in coal form corrosive and toxic compounds during coal gasification processes. DOE’s NETL aims to reduce contaminants to parts per billion in order to utilize gasification gas streams in fuel cell applications. Even more stringent requirements are expected if the fuel is to be utilized in chemical production applications. Regenerable hydrogen sulfide removal sorbents have been developed at NETL. These sorbents can remove the hydrogen sulfide to ppb range at 316 °C and at 20 atmospheres. The sorbent can be regenerated with oxygen. Reactivity and physical durability of the sorbent did not change during the multi-cycle tests. The sorbent development work has been extended to include the removal of other major impurities, such as HCl and NH3. The sorbents for HCl removal that are available today are not regenerable. Regenerable HCl removal sorbents have been developed at NETL. These sorbents can remove HCl to ppb range at 300 °C to 500 °C. The sorbent can be regenerated with oxygen. Results of TGA and bench-scale flow reactor tests with both regenerable and non-regenerable HCl removal sorbents will be discussed in the paper. Bench-scale reactor tests were also conducted with NH3 removal sorbents. The results indicated that the sorbents have a high removal capacity and good regenerability during the multi-cycle tests. Future emphasis of the NETL coal gasification/cleanup program is to develop multi-functional sorbents to remove multiple impurities in order to minimize the steps involved in the cleanup systems. To accomplish this goal, a regenerable sorbent capable of removing both HCl and H2S was developed. The results of the TGA conducted with the sorbent to evaluate the feasibility of both H2S and HCl sorption will be discussed in this paper.

Siriwardane, R.V.; Tian, H.; Simonyi, T.; Webster, T.

2007-08-01T23:59:59.000Z

179

THERMALLY SHIELDED MOISTURE REMOVAL DEVICE  

DOE Patents (OSTI)

An apparatus is presented for removing moisture from the air within tanks by condensation upon a cartridge containing liquid air. An insulating shell made in two halves covers the cartridge within the evacuated system. The shell halves are hinged together and are operated by a system of levers from outside the tank with the motion translated through a sylphon bellows to cover and uncover the cartridge. When the condensation of moisture is in process, the insulative shell is moved away from the liquid air cartridge, and during that part of the process when there is no freezing out of moisture, the shell halves are closed on the cell so thnt the accumulated frost is not evaporated. This insulating shell greatly reduces the consumption of liquid air in this condensation process.

Miller, O.E.

1958-08-26T23:59:59.000Z

180

High-Value Fluorine Compounds  

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

Compounds Baseline plans call for production of anhydrous or aqueous Hydrogen Fluoride (HF) from the DU hexafluoride conversion plant and subsequent recycle of these...

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Melter Glass Removal and Dismantlement  

Science Conference Proceedings (OSTI)

The U.S. Department of Energy (DOE) has been using vitrification processes to convert high-level radioactive waste forms into a stable glass for disposal in waste repositories. Vitrification facilities at the Savannah River Site (SRS) and at the West Valley Demonstration Project (WVDP) are converting liquid high-level waste (HLW) by combining it with a glass-forming media to form a borosilicate glass, which will ensure safe long-term storage. Large, slurry fed melters, which are used for this process, were anticipated to have a finite life (on the order of two to three years) at which time they would have to be replaced using remote methods because of the high radiation fields. In actuality the melters useable life spans have, to date, exceeded original life-span estimates. Initial plans called for the removal of failed melters by placing the melter assembly into a container and storing the assembly in a concrete vault on the vitrification plant site pending size-reduction, segregation, containerization, and shipment to appropriate storage facilities. Separate facilities for the processing of the failed melters currently do not exist. Options for handling these melters include (1) locating a facility to conduct the size-reduction, characterization, and containerization as originally planned; (2) long-term storing or disposing of the complete melter assembly; and (3) attempting to refurbish the melter and to reuse the melter assembly. The focus of this report is to look at methods and issues pertinent to size-reduction and/or melter refurbishment in particular, removing the glass as a part of a refurbishment or to reduce contamination levels (thus allowing for disposal of a greater proportion of the melter as low level waste).

Richardson, BS

2000-10-31T23:59:59.000Z

182

Nitrogen removal from natural gas  

SciTech Connect

According to a 1991 Energy Information Administration estimate, U.S. reserves of natural gas are about 165 trillion cubic feet (TCF). To meet the long-term demand for natural gas, new gas fields from these reserves will have to be developed. Gas Research Institute studies reveal that 14% (or about 19 TCF) of known reserves in the United States are subquality due to high nitrogen content. Nitrogen-contaminated natural gas has a low Btu value and must be upgraded by removing the nitrogen. In response to the problem, the Department of Energy is seeking innovative, efficient nitrogen-removal methods. Membrane processes have been considered for natural gas denitrogenation. The challenge, not yet overcome, is to develop membranes with the required nitrogen/methane separation characteristics. Our calculations show that a methane-permeable membrane with a methane/nitrogen selectivity of 4 to 6 would make denitrogenation by a membrane process viable. The objective of Phase I of this project was to show that membranes with this target selectivity can be developed, and that the economics of the process based on these membranes would be competitive. Gas permeation measurements with membranes prepared from two rubbery polymers and a superglassy polymer showed that two of these materials had the target selectivity of 4 to 6 when operated at temperatures below - 20{degrees}C. An economic analysis showed that a process based on these membranes is competitive with other technologies for small streams containing less than 10% nitrogen. Hybrid designs combining membranes with other technologies are suitable for high-flow, higher-nitrogen-content streams.

1997-04-01T23:59:59.000Z

183

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/NETL’s 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

184

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

185

Energy Saving System to Remove Volatile Organic Compounds (VOCs) from Indoor Air  

Scientists at Berkeley Lab have developed a catalyst and deployment devices to improve indoor air quality and reduce ventilation energy needs.

186

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

DOE Patents (OSTI)

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

Siriwardane, Ranjan

1999-09-30T23:59:59.000Z

187

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

DOE Patents (OSTI)

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

Siriwardane, Ranjani

2004-06-01T23:59:59.000Z

188

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

E-Print Network (OSTI)

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

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

2008-01-01T23:59:59.000Z

189

Method for removing heavy metal and nitrogen oxides from flue gas, device for removing heavy metal and nitrogen oxides from flue gas  

DOE Patents (OSTI)

A method for the simultaneous removal of oxides and heavy metals from a fluid is provided comprising combining the fluid with compounds containing alkali and sulfur to create a mixture; spray drying the mixture to create a vapor phase and a solid phase; and isolating the vapor phase from the solid phase. A device is also provided comprising a means for spray-drying flue gas with alkali-sulfide containing liquor at a temperature sufficient to cause the flue gas to react with the compounds so as to create a gaseous fraction and a solid fraction and a means for directing the gaseous fraction to a fabric filter.

Huang, Hann-Sheng; Livengood, Charles David

1997-12-01T23:59:59.000Z

190

Process for removing technetium from iron and other metals  

DOE Patents (OSTI)

Technetium is a radioactive product of the nuclear fission process. During reprocessing of spent or partially spent fuel from nuclear reactors, the technetium can be released and contaminate other, otherwise good, metals. A specific example is equipment in gaseous diffusion uranium enrichment cascades which have been used to process fuel which was returned from reactors, so-called reactor returns. These returns contained volatile technetium compounds which contaminated the metals in the equipment. Present regulations require that technetium be removed before the metal can be re-used at non-radioactive sites. Removing the technetium from contaminated metals has two desirable results. First, the large amount of nonradioactive metal produced by the process herein described can be recycled at a much lower cost than virgin metal can be produced. Second, large amounts of radioactively contaminated metal can be reduced to relatively small amounts of radioactive slag and large amounts of essentially uncontaminated metal. A new and improved process for removing technetium from iron and other metals is described in which between 1/10 atom % and 5 atom % of manganese is added to the contaminated metal in order to replace the technetium.

Leitnaker, James M.; Trowbridge, Lee D.

1997-12-01T23:59:59.000Z

191

Method for removing oxide contamination from silicon carbide powders  

DOE Patents (OSTI)

The described invention is directed to a method for removing oxide contamination in the form of oxygen-containing compounds such as SiO/sub 2/ and B/sub 2/O/sub 3/ from a charge of finely divided silicon carbide. The silicon carbide charge is contacted with a stream of hydrogen fluoride mixed with an inert gas carrier such as argon at a temperature in the range of about 200/sup 0/ to 650/sup 0/C. The oxides in the charge react with the heated hydrogen fluoride to form volatile gaseous fluorides such as SiF/sub 4/ and BF/sub 3/ which pass through the charge along with unreacted hydrogen fluoride and the carrier gas. Any residual gaseous reaction products and hydrogen fluoride remaining in the charge are removed by contacting the charge with the stream of inert gas which also cools the powder to room temperature. The removal of the oxygen contamination by practicing the present method provides silicon carbide powders with desirable pressing and sintering characteristics. 1 tab.

Brynestad, J.; Bamberger, C.E.

1984-08-01T23:59:59.000Z

192

METHOD OF REDUCING PLUTONIUM COMPOUNDS  

DOE Patents (OSTI)

A method is described for reducing plutonium compounds in aqueous solution from a higher to a lower valence state. This reduction of valence is achieved by treating the aqueous solution of higher valence plutonium compounds with hydrogen in contact with an activated platinum catalyst.

Johns, I.B.

1958-06-01T23:59:59.000Z

193

Process for removal of water and silicon mu-oxides from chlorosilanes  

DOE Patents (OSTI)

A scavenger composition having utility for removal of water and silicon mu-oxide impurities from chlorosilanes, such scavenger composition comprising: (a) a support; and (b) associated with the support, one or more compound(s) selected from the group consisting of compounds of the formula: R.sub.a-x MCl.sub.x wherein: M is a metal selected from the group consisting of the monovalent metals lithium, sodium, and potassium; the divalent metals magnesium, strontium, barium, and calcium; and the trivalent metal aluminum; R is alkyl; a is a number equal to the valency of metal M; and x is a number having a value of from 0 to a, inclusive; and wherein said compound(s) of the formula R.sub.a-x MCl.sub.x have been activated for impurity-removal service by a reaction scheme selected from those of the group consisting of: (i) reaction of such compound(s) with hydrogen chloride to form a first reaction product therefrom, followed by reaction of the first reaction product with a chlorosilane of the formula: SiH.sub.4-y Cl.sub.y, wherein y is a number having a value of from 1 to 3, inclusive; and (ii) reaction of such compound(s) with a chlorosilane of the formula: SiH.sub.4-y Cl.sub.y wherein y is a number having a value of 1 to 3, inclusive. A corresponding method of making the scavenger composition, and of purifying a chlorosilane which contains oxygen and silicon mu-oxide impurities, likewise are disclosed, together with a purifier apparatus, in which a bed of the scavenger composition is disposed. The composition, purification process, and purifier apparatus of the invention have utility in purifying gaseous chlorosilanes which are employed in the semiconductor industry as silicon source reagents for forming epitaxial silicon layers.

Tom, Glenn M. (New Milford, CT); McManus, James V. (Danbury, CT)

1992-03-10T23:59:59.000Z

194

Composition, process, and apparatus, for removal of water and silicon mu-oxides from chlorosilanes  

DOE Patents (OSTI)

A scavenger composition having utility for removal of water and silicon mu-oxide impurities from chlorosilanes, such scavenger composition comprising: (a) a support; and (b) associated with the support, one or more compound(s) selected from the group consisting of compounds of the formula: R.sub.a-x MCl.sub.x wherein: M is a metal selected from the group consisting of the monovalent metals lithium, sodium, and potassium; the divalent metals magnesium, strontium, barium, and calcium; and the trivalent metal aluminum; R is alkyl; a is a number equal to the valency of metal M; and x is a number having a value from 0 to a, inclusive; and wherein said compound(s) of the formula R.sub.a-x MCl.sub.x have been activated for impurity-removal service by a reaction scheme selected from those of the group consisting of: (i) reaction of such compound(s) with hydrogen chloride to form a first reaction product therefrom, followed by reaction of the first reaction product with a chlorosilane of the formula: SiH.sub.4"y Cl.sub.y, wherein y is a number having a value of from 1 to 3, inclusive; and (ii) reaction of such compound(s) with a chlorosilane of the formula: SiH.sub.4-y Cl.sub.y wherein y is a number having a value of 1 to 3, inclusive. A corresponding method of making the scavenger composition, and of purifying a chlorosilane which contains oxygen and silicon mu-oxide impurities, likewise are disclosed, together with a purifier apparatus, in which a bed of the scavenger composition is disposed. The composition, purification process, and purifier apparatus of the invention have utility in purifying gaseous chlorosilanes which are employed in the semiconductor industry as silicon source reagents for forming epitaxial silicon layers.

Tom, Glenn M. (New Milford, CT); McManus, James V. (Danbury, CT)

1991-10-15T23:59:59.000Z

195

Devices for collecting chemical compounds  

SciTech Connect

A device for sampling chemical compounds from fixed surfaces and related methods are disclosed. The device may include a vacuum source, a chamber and a sorbent material. The device may utilize vacuum extraction to volatilize the chemical compounds from a fixed surface so that they may be sorbed by the sorbent material. The sorbent material may then be analyzed using conventional thermal desorption/gas chromatography/mass spectrometry (TD/GC/MS) instrumentation to determine presence of the chemical compounds. The methods may include detecting release and presence of one or more chemical compounds and determining the efficacy of decontamination. The device may be useful in collection and analysis of a variety of chemical compounds, such as residual chemical warfare agents, chemical attribution signatures and toxic industrial chemicals.

Scott, Jill R; Groenewold, Gary S

2013-12-24T23:59:59.000Z

196

Application of Metagenomics for Identification of Novel Petroleum Hydrocarbon Degrading Enzymes in Natural Asphalts from the Rancho La Brea Tar Pits  

E-Print Network (OSTI)

and PCR quantification of catechol 2,3-dioxygmase genes from101 Phylogenetic tree of catechol 2,3-dioxygenase genes fromprotocatechuates and catechols. These compounds are further

Baquiran, Jean-Paul Mendoza

2010-01-01T23:59:59.000Z

197

Part 3: Removal Action | Department of Energy  

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

3: Removal Action 3: Removal Action Part 3: Removal Action Question: When may removal actions be initiated? Answer: Removal actions may be initiated when DOE determines that the action will prevent, minimize, stabilize, or eliminate a risk to health or the environment. The NCP specifies that the determination that a risk to health or the environment is appropriate for removal action should be based on: actual or potential exposure of humans, animals, or the food chain the presence of contained hazardous substances that pose a threat of release the threat of migration of the hazardous substances the threat of fire or explosion the availability of an appropriate Federal or State response capability [section 300.415(b)(2)]. In essence, where DOE identifies a threat of exposure to or migration of

198

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly ({gamma}-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly ({gamma}-glutamylcysteinyl)glycines having a particular number of monomer repeat units for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heavy metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, P.J.; Delhaize, E.; Robinson, N.J.; Unkefer, C.J.; Furlong, C.

1988-08-26T23:59:59.000Z

199

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly (.gamma.-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly (.gamma.-glutamylcysteinyl)glycines having a particular number of monomer repeat units for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heavy metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, Paul J. (Los Alamos, NM); Delhaize, Emmanuel (Los Alamos, NM); Robinson, Nigel J. (Durham, GB2); Unkefer, Clifford J. (Los Alamos, NM); Furlong, Clement (Seattle, WA)

1990-01-01T23:59:59.000Z

200

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly (.gamma.-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly (.gamma.-glutamylcysteinyl)glycines having a particular number of monomer repeat unit for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heayv metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, Paul J. (both Los Alamos, NM); Delhaize, Emmanuel (both Los Alamos, NM); Robinson, Nigel J. (Durham, GB2); Unkefer, Clifford J. (Los Alamos, NM); Furlong, Clement (Seattle, WA)

1990-11-13T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Process for particulate removal from coal liquids  

DOE Patents (OSTI)

Suspended solid particulates are removed from liquefied coal products by first subjecting such products to hydroclone action for removal in the underflow of the larger size particulates, and then subjecting the overflow from said hydroclone action, comprising the residual finer particulates, to an electrostatic field in an electrofilter wherein such finer particulates are deposited in the bed of beads of dielectric material on said filter. The beads are periodically cleaned by backwashing to remove the accumulated solids.

Rappe, Gerald C. (Macungie, PA)

1983-01-01T23:59:59.000Z

202

Method for removing contaminants from plastic resin  

Science Conference Proceedings (OSTI)

A resin recycling method that produces essentially contaminant-free synthetic resin material in an environmentally safe and economical manner. The method includes receiving the resin in container form. The containers are then ground into resin particles. The particles are exposed to a solvent, the solvent contacting the resin particles and substantially removing contaminants on the resin particles. After separating the particles and the resin, a solvent removing agent is used to remove any residual solvent remaining on the resin particles after separation.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2008-12-09T23:59:59.000Z

203

Passive Core Decay Heat Removal Performance Guideline  

Science Conference Proceedings (OSTI)

Passive decay heat removal systems operate without pumps when normal heat removal systems are not available. Safety is ensured by confirming that an adequate thermal margin is provided to accommodate various operating conditions, design uncertainties, and degradation. Guidelines to ensure adequate thermal performance are provided for three different system configurations.This report introduces utility systems engineers to the design and operation of passive decay heat removal systems and ...

2013-11-26T23:59:59.000Z

204

Vietnam HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

NNSANews posted a photo: Vietnam HEU Removal A convoy escorting the last highly enriched uranium in Vietnam departs Dalat. Facebook Twitter Youtube Flickr Headlines Jul 23,...

205

Metal Organic Clathrates for Carbon Dioxide Removal  

removal from coal-fired power plant flue gas streams.  Modified variations of the materials can be used in a variety of other fields as well, ...

206

System for removing contaminants from plastic resin  

DOE Patents (OSTI)

A resin recycling system that produces essentially contaminant-free synthetic resin material in an environmentally safe and economical manner. The system includes receiving the resin in container form. A grinder grinds the containers into resin particles. The particles are exposed to a solvent in one or more solvent wash vessels, the solvent contacting the resin particles and substantially removing contaminants on the resin particles. A separator is used to separate the resin particles and the solvent. The resin particles are then placed in solvent removing element where they are exposed to a solvent removing agent which removes any residual solvent remaining on the resin particles after separation.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee' s Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2010-11-23T23:59:59.000Z

207

Improved sulfur removal processes evaluated for IGCC  

SciTech Connect

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

1986-12-01T23:59:59.000Z

208

Method for Removing Precipitates in Biofuel  

ORNL 2010-G00619/jcn UT-B ID 200902314 Method for Removing Precipitates in Biofuel Technology Summary At ORNL the application of ultrasonic energy, or ...

209

Internal Controls Over Classified Computersand Classified Removable...  

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

Classified Removable Media at theLawrence Livermore National Laboratory, IG-0628 Computers are used extensively in the full range of operations at Lawrence Livermore National...

210

Removal of radioisotopes from waste solutions  

DOE Patents (OSTI)

The invention comprises removing radioisotopes from waste liquids or solutions by passing these through filters and through a column containing a suitable salt of phosphoric acid. (Official Gazette)

Kirby, H.W.

1973-10-01T23:59:59.000Z

211

Tritium Removal Facility High Tritium Distillation Simulation.  

E-Print Network (OSTI)

??A dynamic model was developed for the distillation mechanism of the Darlington Tritium Removal Facility. The model was created using the commercial software package MATLAB/Simulink.… (more)

Zahedi, Polad

2013-01-01T23:59:59.000Z

212

Polishing compound for plastic surfaces  

DOE Patents (OSTI)

A polishing compound for plastic surfaces. The compound contains by weight approximately 4 to 17 parts at least one petroleum distillate lubricant, 1 to 6 parts mineral spirits, 2.5 to 15 parts abrasive particles, and 2.5 to 10 parts water. The abrasive is tripoli or a similar material that contains fine particles silica. Preferably, most of the abrasive particles are less than approximately 10 microns, more preferably less than approximately 5 microns in size. The compound is used on PLEXIGLAS.TM., LEXAN.TM., LUCITE.TM., polyvinyl chloride (PVC) and similar plastic materials whenever a smooth, clear polished surface is desired.

Stowell, Michael S. (New Ellenton, SC)

1995-01-01T23:59:59.000Z

213

Polishing compound for plastic surfaces  

DOE Patents (OSTI)

A polishing compound for plastic surfaces is disclosed. The compound contains by weight approximately 4 to 17 parts at least one petroleum distillate lubricant, 1 to 6 parts mineral spirits, 2.5 to 15 parts abrasive particles, and 2.5 to 10 parts water. The abrasive is tripoli or a similar material that contains colloidal silica. Preferably, most of the abrasive particles are less than approximately 10 microns, more preferably less than approximately 5 microns in size. The compound is used on PLEXIGLAS{sup TM}, LEXAN{sup TM}, LUCITE{sup TM}, polyvinyl chloride (PVC) and similar plastic materials whenever a smooth, clear polished surface is desired.

Stowell, M.S.

1993-01-01T23:59:59.000Z

214

Detection of chlorinated aromatic compounds  

SciTech Connect

A method for making a composition for measuring the concentration of chloated aromatic compounds in aqueous fluids, and an optical probe for use with the method. The composition comprises a hydrophobic polymer matrix, preferably polyamide, with a fluorescent indicator uniformly dispersed therein. The indicator fluoresces in the presence of the chlorinated aromatic compounds with an intensity dependent on the concentration of these compounds in the fluid of interest, such as 8-amino-2-naphthalene sulfonate. The probe includes a hollow cylindrical housing that contains the composition in its distal end. The probe admits an aqueous fluid to the probe interior for exposure to the composition. An optical fiber transmits excitation light from a remote source to the composition while the indicator reacts with chlorinated aromatic compounds present in the fluid. The resulting fluorescence light signal is reflected to a second optical fiber that transmits the light to a spectrophotometer for analysis.

Ekechukwu, Amy A. (Augusta, GA)

1996-01-01T23:59:59.000Z

215

COMBUSTION SOURCES OF NITROGEN COMPOUNDS  

E-Print Network (OSTI)

Rasmussen, R.A. (1976). Combustion as a source of nitrousx control for stationary combustion sources. Prog. Energy,CA, March 3-4, 1977 COMBUSTION SOURCES OF NITROGEN COMPOUNDS

Brown, Nancy J.

2011-01-01T23:59:59.000Z

216

Polishing compound for plastic surfaces  

DOE Patents (OSTI)

This invention is comprised of a polishing compound for plastic materials. The compound includes approximately by approximately by weight 25 to 80 parts at least one petroleum distillate lubricant, 1 to 12 parts mineral spirits, 50 to 155 parts abrasive paste, and 15 to 60 parts water. Preferably, the compound includes approximately 37 to 42 parts at least one petroleum distillate lubricant, up to 8 parts mineral spirits, 95 to 110 parts abrasive paste, and 50 to 55 parts water. The proportions of the ingredients are varied in accordance with the particular application. The compound is used on PLEXIGLAS{trademark}, LEXAN{trademark}, LUCITE{trademark}, polyvinyl chloride (PVC), and similar plastic materials whenever a smooth, clear polished surface is desired.

Stowell, M.S.

1991-01-01T23:59:59.000Z

217

Detection of chlorinated aromatic compounds  

DOE Patents (OSTI)

A method for making a composition for measuring the concentration of chlorinated aromatic compounds in aqueous fluids, and an optical probe for use with the method are disclosed. The composition comprises a hydrophobic polymer matrix, preferably polyamide, with a fluorescent indicator uniformly dispersed therein. The indicator fluoresces in the presence of the chlorinated aromatic compounds with an intensity dependent on the concentration of these compounds in the fluid of interest, such as 8-amino-2-naphthalene sulfonate. The probe includes a hollow cylindrical housing that contains the composition in its distal end. The probe admits an aqueous fluid to the probe interior for exposure to the composition. An optical fiber transmits excitation light from a remote source to the composition while the indicator reacts with chlorinated aromatic compounds present in the fluid. The resulting fluorescence light signal is reflected to a second optical fiber that transmits the light to a spectrophotometer for analysis. 5 figs.

Ekechukwu, A.A.

1996-02-06T23:59:59.000Z

218

DISSOLUTION METHOD OF REMOVING BONDING AGENTS  

DOE Patents (OSTI)

A method is given for removing residual aluminumsilicon bonding agents from uranium slugs after the removal of aluminum coatings. To accomplish this the slug is immersed in an aqueous solution about 0.75 N in hydrofluoric acid and about 7 N in nitric acid.

Hyman, H.H.

1960-04-19T23:59:59.000Z

219

Method of removing contaminants from plastic resins  

DOE Patents (OSTI)

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee' s Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2008-11-18T23:59:59.000Z

220

Method for removing contaminants from plastic resin  

Science Conference Proceedings (OSTI)

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2008-12-30T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Method of removing contaminants from plastic resins  

Science Conference Proceedings (OSTI)

A method for removing contaminants from synthetic resin material containers using a first organic solvent system and a second carbon dioxide system. The organic solvent is utilized for removing the contaminants from the synthetic resin material and the carbon dioxide is used to separate any residual organic solvent from the synthetic resin material.

Bohnert,George W. (Harrisonville, MO); Hand,Thomas E. (Lee's Summit, MO); Delaurentiis,Gary M. (Jamestown, CA)

2007-08-07T23:59:59.000Z

222

Global Cut Framework for Removing Symmetries  

Science Conference Proceedings (OSTI)

In this paper, we propose a general technique for removing symmetries in CSPs during search. The idea is to record no-goods, during the exploration of the search tree, whose symmetric counterpart (if any) should be removed. The no-good, called Global ...

Filippo Focacci; Michela Milano

2001-11-01T23:59:59.000Z

223

Aza compounds as anion receptors  

SciTech Connect

A family of aza-ether based compounds including linear, multi-branched and aza-crown ethers is provided. When added to non-aqueous battery electrolytes, the family of aza-ether based compounds acts as neutral receptors to complex the anion moiety of the electrolyte salt thereby increasing the conductivity and the transference number of Li.sup.+ ion in alkali metal batteries.

Lee, Hung Sui (East Setauket, NY); Yang, Xiao-Qing (Port Jefferson Station, NY); McBreen, James (Bellport, NY)

1998-01-06T23:59:59.000Z

224

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

225

Multiple pollutant removal using the condensing heat exchanger. Task 2, Pilot scale IFGT testing  

Science Conference Proceedings (OSTI)

The purpose of Task 2 (IFGT Pilot-Scale Tests at the B&W Alliance Research Center) is to evaluate the emission reduction performance of the Integrated flue Gas Treatment (IFGT) process for coal-fired applications. The IFGT system is a two-stage condensing heat exchanger that captures multiple pollutants - while recovering waste heat. The IFGT technology offers the potential of a addressing the emission of SO{sub 2} and particulate from electric utilities currently regulated under the Phase I and Phase II requirements defined in Title IV, and many of the air pollutants that will soon be regulated under Title III of the Clean Air Act. The performance data will be obtained at pilot-scale conditions similar to full-scale operating systems. The task 2 IFGT tests have been designed to investigate several aspects of IFGT process conditions at a broader range of variable than would be feasible at a larger scale facility. The performance parameters that will be investigated are as follows: SO{sub 2} removal; particulate removal; removal of mercury and other heavy metals; NO{sub x} removal; HF and HCl removal; NH{sub 3} removal; ammonia-sulfur compounds generation; and steam injection for particle removal. For all of the pollutant removal tests, removal efficiency will be based on measurements at the inlet and outlet of the IFGT facility. Heat recovery measurements will also be made during these tests to demonstrate the heat recovery provided by the IFGT technology. This report provides the Final Test Plan for the first coal tested in the Task 2 pilot-scale IFGT tests.

Jankura, B.J.

1996-01-01T23:59:59.000Z

226

Compound cast product and method for producing a compound cast product  

DOE Patents (OSTI)

A compound cast product is formed in a casting mold (14) having a mold cavity (16) sized and shaped to form the cast product. A plurality of injectors (24) is supported from a bottom side (26) of the casting mold (14). The injectors (24) are in fluid communication with the mold cavity (16) through the bottom side (26) of the casting mold (14). A molten material holder furnace (12) is located beneath the casting mold (14). The holder furnace (12) defines molten material receiving chambers (36) configured to separately contain supplies of two different molten materials (37, 38). The holder furnace (12) is positioned such that the injectors (24) extend downward into the receiving chamber (36). The receiving chamber (36) is separated into at least two different flow circuits (51, 52). A first molten material (37) is received in a first flow circuit (51), and a second molten material (38) is received into a second flow circuit (52). The first and second molten materials (37, 38) are injected into the mold cavity (16) by the injectors (24) acting against the force of gravity. The injectors (24) are positioned such that the first and second molten materials (37, 38) are injected into different areas of the mold cavity (16). The molten materials (37, 38) are allowed to solidify and the resulting compound cast product is removed from the mold cavity (16).

Meyer, Thomas N. (3987 Murray Highlands Cir., Murrysville, PA 15668-1747); Viswanathan, Srinath (1104 Albermarle La., Knoxville, TN 37923)

2002-09-17T23:59:59.000Z

227

Method for purifying bidentate organophosphorus compounds  

DOE Patents (OSTI)

Bidentate organophosphorus compounds useful for extracting actinide elements from acidic nuclear waste solutions are purified of undesirable acidic impurities by contacting the compounds with ethylene glycol which preferentially extracts the impurities found in technical grade bidentate compounds.

Schulz, Wallace W. (Richland, WA)

1977-01-01T23:59:59.000Z

228

DEVELOPMENT OF CHEMICAL REDUCTION AND AIR STRIPPING PROCESSES TO REMOVE MERCURY FROM WASTEWATER  

SciTech Connect

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

Jackson, D.; Looney, B.; Craig, B.; Thompson, M.; Kmetz, T.

2013-07-10T23:59:59.000Z

229

Actinide removal from nitric acid waste streams  

SciTech Connect

Actinide separations research at the Rocky Flats Plant (RFP) has found ways to significantly improve plutonium secondary recovery and americium removal from nitric acid waste streams generated by plutonium purification operations. Capacity and breakthrough studies show anion exchange with Dowex 1x4 (50 to 100 mesh) to be superior for secondary recovery of plutonium. Extraction chromatography with TOPO(tri-n-octyl-phosphine oxide) on XAD-4 removes the final traces of plutonium, including hydrolytic polymer. Partial neutralization and solid supported liquid membrane transfer removes americium for sorption on discardable inorganic ion exchangers, potentially allowing for non-TRU waste disposal.

Muscatello, A.C.; Navratil, J.D.

1986-01-01T23:59:59.000Z

230

In situ removal of contamination from soil  

DOE Patents (OSTI)

A process of remediation of cationic heavy metal contamination from soil utilizes gas phase manipulation to inhibit biodegradation of a chelating agent that is used in an electrokinesis process to remove the contamination, and further gas phase manipulation to stimulate biodegradation of the chelating agent after the contamination has been removed. The process ensures that the chelating agent is not attacked by bioorganisms in the soil prior to removal of the contamination, and that the chelating agent does not remain as a new contaminant after the process is completed.

Lindgren, Eric R. (Albuquerque, NM); Brady, Patrick V. (Albuquerque, NM)

1997-01-01T23:59:59.000Z

231

Method for changing removable bearing for a wind turbine generator  

DOE Patents (OSTI)

A wind generator having removable change-out bearings includes a rotor and a stator, locking bolts configured to lock the rotor and stator, a removable bearing sub-assembly having at least one shrunk-on bearing installed, and removable mounting bolts configured to engage the bearing sub-assembly and to allow the removable bearing sub-assembly to be removed when the removable mounting bolts are removed.

Bagepalli, Bharat Sampathkumaran (Niskayuna, NY); Jansen, Patrick Lee (Scotia, NY), Gadre; Aniruddha Dattatraya (Rexford, NY)

2008-04-22T23:59:59.000Z

232

Uranium Compounds and Other Natural Radioactivities  

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

X-ray Science Division XSD Groups Industry Argonne Home Advanced Photon Source Uranium Compounds and Other Natural Radioactivities Uranium containing compounds and other...

233

compound queries | OpenEI Community  

Open Energy Info (EERE)

- 15:22 Multicolor Maps from Compound Queries ask queries compound queries developer Google maps maps multicolor result formats results Semantic Mediawiki Hi all, Recently, a...

234

Method for removal of plutonium impurity from americium oxides and fluorides  

SciTech Connect

Method for removal of plutonium impurity from americium oxides and fluorides. AmF.sub.4 is not further oxidized to AmF.sub.6 by the application of O.sub.2 F at room temperature, while plutonium compounds present in the americium sample are fluorinated to volatile PuF.sub.6, which can readily be separated therefrom, leaving the purified americium oxides and/or fluorides as the solid tetrafluoride.

FitzPatrick, John R. (Los Alamos, NM); Dunn, Jerry G. (Los Alamos, NM); Avens, Larry R. (Los Alamos, NM)

1987-01-01T23:59:59.000Z

235

Solid Sorbents for Removal of Carbon Dioxide from Gas Streams at Low Temperatures  

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

Sorbents for Removal of Carbon Dioxide from Sorbents for Removal of Carbon Dioxide from Gas Streams at Low Temperatures Opportunity The Department of Energy's National Energy Technology Laboratory is seeking licensing partners interested in implementing United States Patent Number 6,908,497 entitled "Solid Sorbents for Removal of Carbon Dioxide from Gas Streams at Low Temperatures." Disclosed in this patent is a new low-cost carbon dioxide (CO 2 ) sorbent that can be used in large-scale gas-solid processes. Researchers have developed a new method to prepare these sorbents by treating substrates with an amine and/or an ether in a way that either one comprises at least 50 weight percent of the sorbent. The sorbent captures compounds contained in gaseous fluids through chemisorptions and/or

236

Methods of removing a constituent from a feed stream using adsorption media  

SciTech Connect

A method of producing an adsorption medium to remove at least one constituent from a feed stream. The method comprises dissolving and/or suspending at least one metal compound in a solvent to form a metal solution, dissolving polyacrylonitrile into the metal solution to form a PAN-metal solution, and depositing the PAN-metal solution into a quenching bath to produce the adsorption medium. The at least one constituent, such as arsenic, selenium, or antimony, is removed from the feed stream by passing the feed stream through the adsorption medium. An adsorption medium having an increased metal loading and increased capacity for arresting the at least one constituent to be removed is also disclosed. The adsorption medium includes a polyacrylonitrile matrix and at least one metal hydroxide incorporated into the polyacrylonitrile matrix.

Tranter, Troy J. (Idaho Falls, ID); Mann, Nicholas R. (Rigby, ID); Todd, Terry A. (Aberdeen, ID); Herbst, Ronald S. (Idaho Falls, ID)

2011-05-24T23:59:59.000Z

237

Removal Action Plan for the Accelerated Retrieval Project for a Described Area within Pit 4  

SciTech Connect

This Removal Action Plan documents the plan for implementation of the Comprehensive Environmental Response, Compenstion, and Liability Act non-time-critical removal action to be performed by the Accelerated Retrieval Project. The focus of the action is the limited excavation and retrieval of selected waste streams from a designated portion of the Radioactive Waste Management Complex Subsurface Disposal Area that are contaminated with volatile organic compounds, isotopes of uranium, or transuranic radionuclides. The selected retrieval area is approximately 0.2 ha (1/2 acre) and is located in the eastern portion of Pit 4. The proposed project is referred to as the Accelerated Retrieval Project. This Removal Action Plan details the major work elements, operations approach, and schedule, and summarizes the environmental, safety and health, and waste management considerations associated with the project.

A. M. Tyson

2006-08-01T23:59:59.000Z

238

Kazakhstan HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Kazakhstan HEU Removal | National Nuclear Security Administration Kazakhstan HEU Removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > Kazakhstan HEU Removal Kazakhstan HEU Removal Location Kazakhstan United States 48° 59' 44.1492" N, 67° 3' 37.9692" E See map: Google Maps Printer-friendly version Printer-friendly version

239

Sweden Plutonium Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Sweden Plutonium Removal | National Nuclear Security Administration Sweden Plutonium Removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > Sweden Plutonium Removal Sweden Plutonium Removal Location Sweden United States 62° 24' 4.4136" N, 15° 22' 51.096" E See map: Google Maps Printer-friendly version Printer-friendly version

240

Hungary HEU removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

removal | National Nuclear Security Administration removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > Hungary HEU removal Hungary HEU removal Location Hungary United States 47° 11' 51.6336" N, 19° 41' 15" E See map: Google Maps Printer-friendly version Printer-friendly version Javascript is required to view this map.

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Mexico HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Removal | National Nuclear Security Administration Removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > Mexico HEU Removal Mexico HEU Removal Location Mexico United States 24° 24' 35.298" N, 102° 49' 55.3116" W See map: Google Maps Printer-friendly version Printer-friendly version Javascript is required to view this map.

242

Removal of volatile materials from forepump oil  

Science Conference Proceedings (OSTI)

A method of clearing condensable vapors from forepump oil is described. Air is bubbled though the oil reservoir removing volatile material from the oil and allowing continuous pumping of materials by non?vented pumps.

Paul P. Nicole

1980-01-01T23:59:59.000Z

243

Method of removing polychlorinated biphenyl from oil  

DOE Patents (OSTI)

Polychlorinated biphenyls are removed from oil by extracting the biphenyls into methanol. The mixture of methanol and extracted biphenyls is distilled to separate methanol therefrom, and the methanol is recycled for further use in extraction of biphenyls from oil.

Cook, Gus T. (Paducah, KY); Holshouser, Stephen K. (Boaz, KY); Coleman, Richard M. (Paducah, KY); Harless, Charles E. (Smithland, KY); Whinnery, III, Walter N. (Paducah, KY)

1983-01-01T23:59:59.000Z

244

Method of removing polychlorinated biphenyl from oil  

DOE Patents (OSTI)

Polychlorinated biphenyls are removed from oil by extracting the biphenyls into methanol. The mixture of methanol and extracted biphenyls is distilled to separate methanol therefrom, and the methanol is recycled for further use in extraction of biphenyls from oil.

Cook, G.T.; Holshouser, S.K.; Coleman, R.M.; Harless, C.E.; Whinnery, W.N. III

1982-03-17T23:59:59.000Z

245

Chile HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

HEU Removal Location United States 25 28' 1.4916" S, 69 33' 55.548" W See map: Google Maps Printer-friendly version Printer-friendly version Javascript is required to view...

246

France HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

HEU Removal Location United States 45 44' 20.0544" N, 2 17' 6.5616" E See map: Google Maps Printer-friendly version Printer-friendly version Javascript is required to view...

247

Libya HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Removal Location Libya United States 27 34' 9.5448" N, 17 24' 8.4384" E See map: Google Maps Printer-friendly version Printer-friendly version Javascript is required to view...

248

Install Removable Insulation on Valves and Fittings  

Science Conference Proceedings (OSTI)

This revised ITP tip sheet on installing removable insulation on valves and fittings provides how-to advice for improving the system using low-cost, proven practices and technologies.

Not Available

2006-01-01T23:59:59.000Z

249

Turkey HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Turkey HEU Removal | National Nuclear Security Administration Turkey HEU Removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > Turkey HEU Removal Turkey HEU Removal Location Turkey United States 38° 26' 50.2044" N, 40° 15' 14.0616" E See map: Google Maps Printer-friendly version Printer-friendly version

250

Multi-component removal in flue gas by aqua ammonia  

DOE Patents (OSTI)

A new method for the removal of environmental compounds from gaseous streams, in particular, flue gas streams. The new method involves first oxidizing some or all of the acid anhydrides contained in the gas stream such as sulfur dioxide (SO.sub.2) and nitric oxide (NO) and nitrous oxide (N.sub.2O) to sulfur trioxide (SO.sub.3) and nitrogen dioxide (NO.sub.2). The gas stream is subsequently treated with aqua ammonia or ammonium hydroxide which captures the compounds via chemical absorption through acid-base or neutralization reactions. The products of the reactions can be collected as slurries, dewatered, and dried for use as fertilizers, or once the slurries have been dewatered, used directly as fertilizers. The ammonium hydroxide can be regenerated and recycled for use via thermal decomposition of ammonium bicarbonate, one of the products formed. There are alternative embodiments which entail stoichiometric scrubbing of nitrogen oxides and sulfur oxides with subsequent separate scrubbing of carbon dioxide.

Yeh, James T. (Bethel Park, PA); Pennline, Henry W. (Bethel Park, PA)

2007-08-14T23:59:59.000Z

251

Laser removal of sludge from steam generators  

SciTech Connect

A method of removing unwanted chemical deposits known as sludge from the metal surfaces of steam generators with laser energy is provided. Laser energy of a certain power density, of a critical wavelength and frequency, is intermittently focused on the sludge deposits to vaporize them so that the surfaces are cleaned without affecting the metal surface (sludge substrate). Fiberoptic tubes are utilized for laser beam transmission and beam direction. Fiberoptics are also utilized to monitor laser operation and sludge removal.

Nachbar, Henry D. (Ballston Lake, NY)

1990-01-01T23:59:59.000Z

252

Warm Mix Asphalt Technologies and Research European countries are using technologies that appear to allow a reduction in the temperatures at  

E-Print Network (OSTI)

gas for large scale Fischer-Tropsch synthesis." American Chemical Society, Division of Petroleum unit · Pre-reformer · Auto-thermal reformer (ATR) · Fired heater CO2 removal (optional) Fischer-Tropsch (FT) reactor: slurry bubble column reactor Fischer-Tropsch products separation #12;8M. Panahi, S

Mukherjee, Amlan

253

Trunnion Collar Removal Machine - Gap Analysis Table  

SciTech Connect

The purpose of this document is to review the existing the trunnion collar removal machine against the ''Nuclear Safety Design Bases for License Application'' (NSDB) [Ref. 10] requirements and to identify codes and standards and supplemental requirements to meet these requirements. If these codes and standards can not fully meet these requirements then a ''gap'' is identified. These gaps will be identified here and addressed using the ''Trunnion Collar Removal Machine Design Development Plan'' [Ref. 15]. The codes and standards, supplemental requirements, and design development requirements for the trunnion collar removal machine are provided in the gap analysis table (Appendix A, Table 1). Because the trunnion collar removal machine is credited with performing functions important to safety (ITS) in the NSDB [Ref. 10], design basis requirements are applicable to ensure equipment is available and performs required safety functions when needed. The gap analysis table is used to identify design objectives and provide a means to satisfy safety requirements. To ensure that the trunnion collar removal machine performs required safety functions and meets performance criteria, this portion of the gap analysis tables supplies codes and standards sections and the supplemental requirements and identifies design development requirements, if needed.

M. Johnson

2005-06-27T23:59:59.000Z

254

Hydrogen Removal From Heating Oil of a Parabolic Trough ...  

Hydrogen Removal From Heating Oil of a Parabolic Trough Increases the Life of the Trough and its Components A Method to Selectively Remove & Measure Hydrogen Gas from ...

255

An Experimental Study of Chemical Oxygen Demand Removal from ...  

Science Conference Proceedings (OSTI)

The experimental results showed that the refractory organics in coking wastewater can be effectively removed by this process, and COD removal efficiency was ...

256

Michigan Nonhydrocarbon Gases Removed from Natural Gas (Million...  

U.S. Energy Information Administration (EIA) Indexed Site

Date: 10312013 Referring Pages: Nonhydrocarbon Gases Removed from Natural Gas Michigan Natural Gas Gross Withdrawals and Production Nonhydrocarbon Gases Removed from...

257

Salt Fluxes for Alkali and Alkaline Earth Element Removal from ...  

Science Conference Proceedings (OSTI)

Sep 1, 2001... for Alkali and Alkaline Earth Element Removal from Molten Aluminum ... Solid chloride salts containing MgC2 can be used to remove alkali ...

258

Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million...  

Gasoline and Diesel Fuel Update (EIA)

Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3...

259

South Dakota Natural Gas Removed from Natural Gas (Million Cubic...  

U.S. Energy Information Administration (EIA) Indexed Site

View History: Monthly Annual Download Data (XLS File) South Dakota Natural Gas Removed from Natural Gas (Million Cubic Feet) South Dakota Natural Gas Removed from Natural Gas...

260

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a molecular sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene to about the mid point of the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 figures.

Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

1993-09-07T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a molecular sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 fig.

Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

1994-06-14T23:59:59.000Z

262

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 fig.

Smith, L.A. Jr.

1989-07-18T23:59:59.000Z

263

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene to about the mid point of the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

Smith, Jr., Lawrence A. (Bellaire, TX); Arganbright, Robert P. (Seabrook, TX); Hearn, Dennis (Houston, TX)

1993-01-01T23:59:59.000Z

264

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

Smith, Jr., Lawrence A. (Bellaire, TX); Arganbright, Robert P. (Seabrook, TX); Hearn, Dennis (Houston, TX)

1994-01-01T23:59:59.000Z

265

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

Smith, Jr., Lawrence A. (Houston, TX)

1989-01-01T23:59:59.000Z

266

Possible explosive compounds in the Savannah River Site Tank Farm facilities. Revision 1  

SciTech Connect

Since 1970, many studies have been conducted concerning the potential for explosive compounds in tank farm operations including ammonium nitrate, metal oxalates, and silver and mercury compounds. The study currently in progress is the most comprehensive to date, encompassing all previous studies and extending the scope to include all compounds that could be formed from the known species in SRS wastes. In addition to waste storage, the study also considers waste removal and waste processing operations. The total number of possible explosive compounds is so large that it would not be useful to list them all here. Instead, only those compounds are listed that are known to be present or could conceivably be formed from material that is known to be present in the waste. The general approach to the problem is: identify all of the constituents that are known to be present in the waste together with those that might be present from possible chemical and radiolytic reactions, determine the compounds that could be formed from these constituents, compare these compounds with those listed in the literature, and assess the formation and stability of these compounds against the conditions existing in the tank farm facilities.

Hobbs, D.T.

1995-04-27T23:59:59.000Z

267

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

268

Technetium Removal Using Tc-Goethite Coprecipitation  

SciTech Connect

This report describes the results from laboratory tests performed at Pacific Northwest National Laboratory for the U.S. Department of Energy (DOE) EM-31 Support Program (EMSP) subtask, “Low temperature waste forms coupled with technetium removal using an alternative immobilization process such as Fe(II) treated-goethite precipitation” to increase our understanding of 99Tc long-term stability in goethite mineral form and the process that controls the 99Tc(VII) reduction and removal by the final Fe (oxy)hydroxide forms. The overall objectives of this task were to 1) evaluate the transformation process of Fe (oxy)hydroxide solids to the more crystalline goethite (?-FeOOH) mineral for 99Tc removal and 2) determine the mechanism that limits 99Tc(IV) reoxidation in Fe(II)-treated 99Tc-goethite mineral and 3) evaluate whether there is a long-term 99Tcoxidation state change for Tc sequestered in the iron solids.

Um, Wooyong; Wang, Guohui; Jung, Hun Bok; Peterson, Reid A.

2013-11-18T23:59:59.000Z

269

Process for removing metals from water  

DOE Patents (OSTI)

A process for removing metals from water including the steps of prefiltering solids from the water, adjusting the pH to between about 2 and 3, reducing the amount of dissolved oxygen in the water, increasing the pH to between about 6 and 8, adding water-soluble sulfide to precipitate insoluble sulfide- and hydroxide-forming metals, adding a containing floc, and postfiltering the resultant solution. The postfiltered solution may optionally be eluted through an ion exchange resin to remove residual metal ions. 2 tabs.

Napier, J.M.; Hancher, C.M.; Hackett, G.D.

1987-06-29T23:59:59.000Z

270

Removal of uranium from aqueous HF solutions  

DOE Patents (OSTI)

This invention is a simple and effective method for removing uranium from aqueous HF solutions containing trace quantities of the same. The method comprises contacting the solution with particulate calcium fluoride to form uranium-bearing particulates, permitting the particulates to settle, and separting the solution from the settled particulates. The CaF.sub.2 is selected to have a nitrogen surface area in a selected range and is employed in an amount providing a calcium fluoride/uranium weight ratio in a selected range. As applied to dilute HF solutions containing 120 ppm uranium, the method removes at least 92% of the uranium, without introducing contaminants to the product solution.

Pulley, Howard (West Paducah, KY); Seltzer, Steven F. (Paducah, KY)

1980-01-01T23:59:59.000Z

271

Removal of uranium from aqueous HF solutions  

Science Conference Proceedings (OSTI)

This invention is a simple and effective method for removing uranium from aqueous HF solutions containing trace quantities of the same. The method comprises contacting the solution with particulate calcium fluoride to form uranium-bearing particulates, permitting the particulates to settle, and separating the solution from the settled particulates. The CaF2 is selected to have a nitrogen surface area in a selected range and is employed in an amount providing a calcium fluoride/uranium weight ratio in a selected range. As applied to dilute HF solutions containing 120 ppm uranium, the method removes at least 92% of the uranium without introducing contaminants to the product solution.

Pulley, H.; Seltzer, S.F.

1980-11-18T23:59:59.000Z

272

Method of removing cesium from steam  

SciTech Connect

Method for removal of radioactive cesium from a hot vapor, such as high temperature steam, including the steps of passing input hot vapor containing radioactive cesium into a bed of silicate glass particles and chemically incorporating radioactive cesium in the silicate glass particles at a temperature of at least about 700.degree. F.

Carson, Jr., Neill J. (Clarendon Hills, IL); Noland, Robert A. (Oak Park, IL); Ruther, Westly E. (Skokie, IL)

1991-01-01T23:59:59.000Z

273

Pentek metal coating removal system: Baseline report  

SciTech Connect

The Pentek coating removal technology was tested and is being evaluated at Florida International University (FIU) as a baseline technology. In conjunction with FIU`s evaluation of efficiency and cost, this report covers evaluation conducted for safety and health issues. It is a commercially available technology and has been used for various projects at locations throughout the country. The Pentek coating removal system consisted of the ROTO-PEEN Scaler, CORNER-CUTTER{reg_sign}, and VAC-PAC{reg_sign}. They are designed to remove coatings from steel, concrete, brick, and wood. The Scaler uses 3M Roto Peen tungsten carbide cutters while the CORNER-CUTTER{reg_sign} uses solid needles for descaling activities. These hand tools are used with the VAC-PAC{reg_sign} vacuum system to capture dust and debris as removal of the coating takes place. The safety and health evaluation during the testing demonstration focused on two main areas of exposure: dust and noise. Dust exposure minimal, but noise exposure was significant. Further testing for each exposure is recommended because of the environment where the testing demonstration took place. It is feasible that the dust and noise levels will be higher in an enclosed operating environment of different construction. In addition, other areas of concern found were arm-hand vibration, whole-body, ergonomics, heat stress, tripping hazards, electrical hazards, machine guarding, and lockout/tagout.

1997-07-31T23:59:59.000Z

274

ASBESTOS PIPE-INSULATION REMOVAL ROBOT SYSTEM  

SciTech Connect

This final topical report details the development, experimentation and field-testing activities for a robotic asbestos pipe-insulation removal robot system developed for use within the DOE's weapon complex as part of their ER and WM program, as well as in industrial abatement. The engineering development, regulatory compliance, cost-benefit and field-trial experiences gathered through this program are summarized.

Unknown

2000-09-15T23:59:59.000Z

275

Method of preparation of removable syntactic foam  

DOE Patents (OSTI)

Easily removable, environmentally safe, low-density, syntactic foams are disclosed which are prepared by mixing insoluble microballoons with a solution of water and/or alcohol-soluble polymer to produce a pourable slurry, optionally vacuum filtering the slurry in varying degrees to remove unwanted solvent and solute polymer, and drying to remove residual solvent. The properties of the foams can be controlled by the concentration and physical properties of the polymer, and by the size and properties of the microballoons. The suggested solute polymers are non-toxic and soluble in environmentally safe solvents such as water or low-molecular weight alcohols. The syntactic foams produced by this process are particularly useful in those applications where ease of removability is beneficial, and could find use in packaging recoverable electronic components, in drilling and mining applications, in building trades, in art works, in the entertainment industry for special effects, in manufacturing as temporary fixtures, in agriculture as temporary supports and containers and for delivery of fertilizer, in medicine as casts and splints, as temporary thermal barriers, as temporary protective covers for fragile objects, as filters for particulate matter, which matter may be easily recovered upon exposure to a solvent, as in-situ valves (for one-time use) which go from maximum to minimum impedance when solvent flows through, and for the automatic opening or closing of spring-loaded, mechanical switches upon exposure to a solvent, among other applications.

Arnold, Jr., Charles (Albuquerque, NM); Derzon, Dora K. (Albuquerque, NM); Nelson, Jill S. (Albuquerque, NM); Rand, Peter B. (Albuquerque, NM)

1995-01-01T23:59:59.000Z

276

Process for removing carbon from uranium  

DOE Patents (OSTI)

Carbon contamination is removed from uranium and uranium alloys by heating in inert atmosphere to 700.degree.-1900.degree.C in effective contact with yttrium to cause carbon in the uranium to react with the yttrium. The yttrium is either in direct contact with the contaminated uranium or in indirect contact by means of an intermediate transport medium.

Powell, George L. (Oak Ridge, TN); Holcombe, Jr., Cressie E. (Knoxville, TN)

1976-01-01T23:59:59.000Z

277

Heat exchanger with a removable tube section  

DOE Patents (OSTI)

A heat exchanger is described in which the tube sheet is secured against primary liquid pressure, but which allows for easy removal of the tube section. The tube section is supported by a flange which is secured by a number of shear blocks, each of which extends into a slot which is immovable with respect to the outer shell of the heat exchanger. (auth)

Wolowodiuk, W.; Anelli, J.

1975-07-29T23:59:59.000Z

278

REMOVAL OF CHLORIDE FROM AQUEOUS SOLUTIONS  

DOE Patents (OSTI)

The removal of chlorides from aqueons solutions is described. The process involves contacting the aqueous chloride containing solution with a benzene solution about 0.005 M in phenyl mercuric acetate whereby the chloride anions are taken up by the organic phase and separating the organic phase from the aqueous solutions.

Schulz, W.W.

1959-08-01T23:59:59.000Z

279

Method of preparation of removable syntactic foam  

DOE Patents (OSTI)

Easily removable, environmentally safe, low-density, syntactic foams are disclosed which are prepared by mixing insoluble microballoons with a solution of water and/or alcohol-soluble polymer to produce a pourable slurry, optionally vacuum filtering the slurry in varying degrees to remove unwanted solvent and solute polymer, and drying to remove residual solvent. The properties of the foams can be controlled by the concentration and physical properties of the polymer, and by the size and properties of the microballoons. The suggested solute polymers are non-toxic and soluble in environmentally safe solvents such as water or low-molecular weight alcohols. The syntactic foams produced by this process are particularly useful in those applications where ease of removability is beneficial, and could find use in packaging recoverable electronic components, in drilling and mining applications, in building trades, in art works, in the entertainment industry for special effects, in manufacturing as temporary fixtures, in agriculture as temporary supports and containers and for delivery of fertilizer, in medicine as casts and splints, as temporary thermal barriers, as temporary protective covers for fragile objects, as filters for particulate matter, which matter may be easily recovered upon exposure to a solvent, as in-situ valves (for one-time use) which go from maximum to minimum impedance when solvent flows through, and for the automatic opening or closing of spring-loaded, mechanical switches upon exposure to a solvent, among other applications. 1 fig.

Arnold, C. Jr.; Derzon, D.K.; Nelson, J.S.; Rand, P.B.

1995-07-11T23:59:59.000Z

280

Effect of Outside Air Ventilation Rate on Volatile Organic Compound  

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

Outside Air Ventilation Rate on Volatile Organic Compound Outside Air Ventilation Rate on Volatile Organic Compound Concentrations in a Call Center Title Effect of Outside Air Ventilation Rate on Volatile Organic Compound Concentrations in a Call Center Publication Type Journal Article Year of Publication 2003 Authors Hodgson, Alfred T., David Faulkner, Douglas P. Sullivan, Dennis L. DiBartolomeo, Marion L. Russell, and William J. Fisk Journal Atmospheric Environment Volume 37 Start Page Chapter Pagination 5517-5528 Abstract A study of the relationship between outside air ventilation rate and concentrations of volatile organic compounds (VOCs) generated indoors was conducted in a call center office building. The building, with two floors and a floor area of 4,600 m2, was located in the San Francisco Bay Area, CA. Ventilation rates were manipulated with the building's four air handling units (AHUs). VOC concentrations in the AHU returns were measured on seven days during a 13-week period. VOC emission factors were determined for individual zones on days when they were operating at near steady-state conditions. The emission factor data were subjected to principal component (PC) analysis to identify groups of co-varying compounds. Potential sources of the PC vectors were ascribed based on information from the literature supporting the associations. Two vectors with high loadings of compounds including formaldehyde, 2,2,4-trimethyl-1,3- pentanediol monoisobutyrate, decamethylcyclopentasiloxane (d5 siloxane), and isoprene likely identified occupant-related sources. One vector likely represented emissions from building materials. Another vector represented emissions of solvents from cleaning products. The relationships between indoor minus outdoor VOC concentrations and ventilation rate were qualitatively examined for eight VOCs. Of these, acetaldehyde and hexanal, which were likely associated with material sources, and d5 siloxane exhibited general trends of higher concentrations at lower ventilation rates. For other compounds, the operation of the building and variations in pollutant generation and removal rates apparently combined to obscure the inverse relationship between VOC concentrations and ventilation. This result emphasizes the importance of utilizing source control measures, in addition to adequate ventilation, to limit concentrations of VOCs of concern in office buildings

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281

Feedback Capacity of the Compound Channel  

E-Print Network (OSTI)

In this work, we find the capacity of a compound finite-state channel (FSC) with time-invariant deterministic feedback. We consider the use of fixed length block codes over the compound channel. Our achievability result ...

Shrader, Brooke E.

282

Recovery and removal of mercury from mixed wastes. Final report, September 1994--June 1995  

SciTech Connect

In recognition of the major environmental problem created by mercury contamination of wastes and soils at an estimated 200,000 sites along US natural gas and oil pipelines and at a number of government facilities, including Oak Ridge, Savannah River, Hanford, and Rocky Flats, the US Department of Energy (DOE) is seeking an effective and economical process for removing mercury from various DOE waste streams in order to allow the base waste streams to be treated by means of conventional technologies. In response to the need for Unproved mercury decontamination technology, Mercury Recovery Services (MRS) has developed and commercialized a thermal treatment process for the recovery of mercury from contaminated soils and industrial wastes. The objectives of this program were to: demonstrate the technical and economic feasibility of the MRS process to successfully remove and recover mercury from low-level mixed waste containing mercury compounds (HgO, HgS, HgCl{sub 2}) and selected heavy metal compounds (PbO, CdO); determine optimum processing conditions required to consistently reduce the residual total mercury content to 1 mg/kg while rendering the treated product nontoxic as determined by TCLP methods; and provide an accurate estimate of the capital and operating costs for a commercial processing facility designed specifically to remove and recovery mercury from various waste streams of interest at DOE facilities. These objectives were achieved in a four-stage demonstration program described within with results.

Sutton, W.F.; Weyand, T.E.; Koshinski, C.J.

1995-06-01T23:59:59.000Z

283

The Compound Capacity of Polar Codes  

E-Print Network (OSTI)

We consider the compound capacity of polar codes under successive cancellation decoding for a collection of binary-input memoryless output-symmetric channels. By deriving a sequence of upper and lower bounds, we show that in general the compound capacity under successive decoding is strictly smaller than the unrestricted compound capacity.

Hassani, S Hamed; Urbanke, Ruediger

2009-01-01T23:59:59.000Z

284

Thin films of mixed metal compounds  

DOE Patents (OSTI)

A compositionally uniform thin film of a mixed metal compound is formed by simultaneously evaporating a first metal compound and a second metal compound from independent sources. The mean free path between the vapor particles is reduced by a gas and the mixed vapors are deposited uniformly. The invention finds particular utility in forming thin film heterojunction solar cells.

Mickelsen, Reid A. (Bellevue, WA); Chen, Wen S. (Seattle, WA)

1985-01-01T23:59:59.000Z

285

INSENSITIVE HIGH-NITROGEN COMPOUNDS  

DOE Green Energy (OSTI)

The conventional approach to developing energetic molecules is to chemically place one or more nitro groups onto a carbon skeleton, which is why the term ''nitration'' is synonymous to explosives preparation. The nitro group carries the oxygen that reacts with the skeletal carbon and hydrogen fuels, which in turn produces the heat and gaseous reaction products necessary for driving an explosive shock. These nitro-containing energetic molecules typically have heats of formation near zero and therefore most of the released energy is derived from the combustion process. Our investigation of the tetrazine, furazan and tetrazole ring systems has offered a different approach to explosives development, where a significant amount of the chemical potential energy is derived from their large positive heats of formation. Because these compounds often contain a large percentage of nitrogen atoms, they are usually regarded as high-nitrogen fuels or explosives. A general artifact of these high-nitrogen compounds is that they are less sensitive to initiation (e.g. by impact) when compared to traditional nitro-containing explosives of similar performances. Using the precursor, 3,6-bis-(3,5-dimethylpyrazol-1-yl)-s-tetrazine, several useful energetic compounds based on the s-tetrazine system have been synthesized and studied. Some of the first compounds are 3,6-diamino-s-tetrazine-1,4-dioxide (LAX-112) and 3,6-dihydrazino-s-tetrazine (DHT). LAX-112 was once extensively studied as an insensitive explosive by Los Alamos; DHT is an example of a high-nitrogen explosive that relies entirely on its heat of formation for sustaining a detonation. Recent synthesis efforts have yielded an azo-s-tetrazine, 3,3'-azobis(6-amino-s-tetrazine) or DAAT, which has a very high positive heat of formation. The compounds, 4,4'-diamino-3,3'-azoxyfurazan (DAAF) and 4,4'-diamino-3,3'-azofurazan (DAAzF), may have important future roles in insensitive explosive applications. Neither DAAF nor DAAzF can be initiated by laboratory impact drop tests, yet both have in some aspects better explosive performances than 1,3,5-triamino-2,4,6-trinitrobenzene TATB--the standard of insensitive high explosives. The thermal stability of DAAzF is equal to that of hexanitrostilbene (HNS), yet it too is a better explosive performer. The recently discovered tetrazol derivative, 3,6-bis-(1H-1,2,3,4-tetrazol-5-ylamino)-s-tetrazine (BTATz) was measured to have exceptional positive heats of formation and to be insensitive to explosive initiation. Because of its high burn rate with low sensitivity to pressure, this material is of great interest to the propellant community.

D. CHAVEZ; ET AL

2001-03-01T23:59:59.000Z

286

Vapor Phase Catalytic Upgrading of Model Biomass-Derived Oxygenate Compounds  

SciTech Connect

When biomass is converted to a liquid bio-oil through pyrolysis, it has a significantly higher oxygen content compared to petroleum fractions. In order to convert the pyrolysis products into infrastructure-compatible fuels, oxygen removal is required. Oxygen removal can be achieved by both hydrotreating (which requires the addition of hydrogen) and decarboxylation or decarbonylation, whereby oxygen is rejected as CO2 and CO, respectively. In the present contribution, a number of catalysts were tested for their activity and selectivity in deoxygenation of model biomass-derived oxygenated compounds (e.g., acetic acid, phenol). Comparison of catalytic activity of materials for different compounds, as well as material characterization results will be discussed. Materials tested will include modified zeolites and supported transition metal catalysts.

Yung, M. M.; Gomez, E.; Kuhn, J. N.

2012-01-01T23:59:59.000Z

287

Improved Cobalt Removal: Field Testing Phase: Effects of Normally Encountered Plant Impurities on Removal Performance  

Science Conference Proceedings (OSTI)

This study examined the effects of plant impurities on cobalt removal from liquid radioactive waste. Improved process knowledge is critical to utilities that are continually working to increase the performance of their low-level waste (LLW) treatment systems. This report provides predictive chemistry information for improved cobalt removal obtained from test work at Catawba Nuclear Station. It also provides test methodologies for performing similar evaluations at other member plants.

2001-11-26T23:59:59.000Z

288

Improved Processes to Remove Naphthenic Acids  

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

Improved Processes to Remove Naphthenic Acids Improved Processes to Remove Naphthenic Acids Final Technical Report (From October 1, 2002 to September 30, 2005) Principle Authors Aihua Zhang, Qisheng Ma, Kangshi Wang, Yongchun Tang (co-PI), William A. Goddard (PI), Date Report was issued: December 9, 2005 DOE Award number: DE-FC26-02NT15383 Name and Address of Submitting Organization California Institute of Technology 1200 East California Blvd., Pasadena, CA91125 Disclaimer This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any

289

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

290

Photoacoustic removal of occlusions from blood vessels  

DOE Patents (OSTI)

Partial or total occlusions of fluid passages within the human body are removed by positioning an array of optical fibers in the passage and directing treatment radiation pulses along the fibers, one at a time, to generate a shock wave and hydrodynamics flows that strike and emulsify the occlusions. A preferred application is the removal of blood clots (thrombin and embolic) from small cerebral vessels to reverse the effects of an ischemic stroke. The operating parameters and techniques are chosen to minimize the amount of heating of the fragile cerebral vessel walls occurring during this photo acoustic treatment. One such technique is the optical monitoring of the existence of hydrodynamics flow generating vapor bubbles when they are expected to occur and stopping the heat generating pulses propagated along an optical fiber that is not generating such bubbles.

Visuri, Steven R. (Livermore, CA); Da Silva, Luiz B. (Danville, CA); Celliers, Peter M. (Berkeley, CA); London, Richard A. (Orinda, CA); Maitland, IV, Duncan J. (Lafayette, CA); Esch, Victor C. (San Francisco, CA)

2002-01-01T23:59:59.000Z

291

Method of removing cesium from steam  

DOE Patents (OSTI)

The foregoing objects of the present invention are achieved by a method for removing radioactive cesium from a hot vapor, such as steam, by a technique wherein the cesium chemically reacts with a filtering material which retains the cesium without causing degradation of the filtering material. The method is carried out at temperatures in the range of from about 700{degree}F to about 1000{degree}F, and even higher, but it preferably is utilized at a temperature of at least about 800{degree}F. The method uses a silica glass which is preferably in the form of spheres as the filter material. The preferred material is a borosilicate glass (Pyrex). The degree of removal of the radioactive cesium from the hot steam or other vapor approaches 90 to 100%.

Carson, N.J. Jr.; Noland, R.A.; Ruther, W.E.

1990-12-02T23:59:59.000Z

292

Removal of Retired Alkali Metal Test Systems  

SciTech Connect

This paper describes the successful effort to remove alkali metals, alkali metal residues, and piping and structures from retired non-radioactive test systems on the Hanford Site. These test systems were used between 1965 and 1982 to support the Fast Flux Test Facility and the Liquid Metal Fast Breeder Reactor Program. A considerable volume of sodium and sodium-potassium alloy (NaK) was successfully recycled to the commercial sector; structural material and electrical material such as wiring was also recycled. Innovative techniques were used to safely remove NaK and its residues from a test system that could not be gravity-drained. The work was done safely, with no environmental issues or significant schedule delays.

Brehm, W. F.; Church, W. R.; Biglin, J. W.

2003-02-26T23:59:59.000Z

293

Acid treatment removes zinc sulfide scale restriction  

Science Conference Proceedings (OSTI)

This paper reports that removal of zinc sulfide (ZnS) scale with acid restored an offshore Louisiana well's production to original rates. The zinc sulfide scale was determined to be in the near well bore area. The selected acid had been proven to control iron sulfide (FeS) scales in sour wells without causing harm to surface production equipment, tubing, and other downhole hardware. The successful removal of the blockage re-established previous production rates with a 105% increase in flowing tubing pressure. On production for a number of months, a high rate, high-pressure offshore well was experiencing unusually rapid pressure and rate declines. A small sample of the restrictive material was obtained during the wire line operations. The well was subsequently shut in while a laboratory analysis determined that zinc sulfide was the major component of the obstruction.

Biggs, K. (Kerr McGee Corp., Lafayette, LA (US)); Allison, D. (Otis Engineering Corp., Lafayette, LA (US)); Ford, W.G.F. (Halliburton Co., Duncan, OK (United States))

1992-08-31T23:59:59.000Z

294

Categorical Exclusion 4568, Crane Removal Project  

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

l)eterminationFornl l)eterminationFornl Project Title: Crane Removal Project (4568) Program or Program Office: Y -12 Site Office Location: Oak Ridge Tennessee Project Description: This work scope is to remove an old legacy crane trolley and old crane operated cab. General Administration/Management DA I - Routine business actions DA2 - Administrative contract amendments DA4 - Interpretations/rulings for existing regulations DA5 - Regulatory interpretations without environmental effect DA6 - Procedural rulemakings upgrade DA7 - Transfer of property, use unchanged DA8 - Award of technical support/M&O/personal service contracts DA9 - Info gathering, analysis, documentation, dissemination, and training DAIO - Reports on non-DOE legislation DA II - Technical advice and planning assistance

295

Trojan PWR Decommissioning: Large Component Removal Project  

Science Conference Proceedings (OSTI)

While the decommissioning of large commercial nuclear plants in the United States is in its infancy, the technical challenges with associated radioactive waste management are clear. This report describes the removal and disposal of four steam generators and one pressurizer from the Trojan nuclear power plant, the first large PWR to be decommissioned in the United States. The report chronicles the problems, successes, and lessons learned in this project, which was completed on schedule and under budget in...

1997-09-29T23:59:59.000Z

296

Removal of iron from impure graphites  

DOE Green Energy (OSTI)

Iron-impregnated and ash-rich graphites have been purified by leaching with gaseous I/sub 2/ at 900/sup 0/C. With addition of H/sub 2/, the rate of removal of impurity iron can be markedly increased and becomes comparable to that obtained with Cl/sub 2/. I/sub 2/ has an advantage in that it can also volatilize Ca and perhaps Ba and Sr.

Growcock, F.B.; Heiser, J.

1979-01-01T23:59:59.000Z

297

Removal of copper from ferrous scrap  

DOE Patents (OSTI)

A process for removing copper from ferrous or other metal scrap in which the scrap is contacted with a polyvalent metal sulfide slag in the presence of an excess of copper-sulfide forming additive to convert the copper to copper sulfide which is extracted into the slag to provide a ratio of copper in the slag to copper in the metal scrap of at least about 10.

Blander, M.; Sinha, S.N.

1987-07-30T23:59:59.000Z

298

Removal of copper from ferrous scrap  

DOE Patents (OSTI)

A process for removing copper from ferrous or other metal scrap in which the scrap is contacted with a polyvalent metal sulfide slag in the presence of an excess of copper-sulfide forming additive to convert the copper to copper sulfide which is extracted into the slag to provide a ratio of copper in the slag to copper in the metal scrap of at least about 10.

Blander, M.; Sinha, S.N.

1990-05-15T23:59:59.000Z

299

Removal of copper from ferrous scrap  

DOE Patents (OSTI)

A process for removing copper from ferrous or other metal scrap in which the scrap is contacted with a polyvalent metal sulfide slag in the presence of an excess of copper-sulfide forming additive to convert the copper to copper sulfide which is extracted into the slag to provide a ratio of copper in the slag to copper in the metal scrap of at least about 10.

Blander, Milton (12833 S. 82nd Ct., Palos Park, IL 60464); Sinha, Shome N. (5748 Drexel, 2A, Chicago, IL 60637)

1990-01-01T23:59:59.000Z

300

Thin films of mixed metal compounds  

DOE Patents (OSTI)

Disclosed is a thin film heterojunction solar cell, said heterojunction comprising a p-type I-III-IV[sub 2] chalcopyrite substrate and an overlying layer of an n-type ternary mixed metal compound wherein said ternary mixed metal compound is applied to said substrate by introducing the vapor of a first metal compound to a vessel containing said substrate from a first vapor source while simultaneously introducing a vapor of a second metal compound from a second vapor source of said vessel, said first and second metals comprising the metal components of said mixed metal compound; independently controlling the vaporization rate of said first and second vapor sources; reducing the mean free path between vapor particles in said vessel, said gas being present in an amount sufficient to induce homogeneity of said vapor mixture; and depositing said mixed metal compound on said substrate in the form of a uniform composition polycrystalline mixed metal compound. 5 figs.

Mickelsen, R.A.; Chen, W.S.

1985-06-11T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

An automatic analysis of Norwegian compounds  

E-Print Network (OSTI)

Introduction The University of Oslo is currently developing an automatic morphosyntactic tagger for Norwegian. 2 A very important module is one which can analyse compounds. Compounding is extremely productive in Norwegian, and it is futile to ever hope for a lexicon (dictionary) that will contain all or even most of the compounds that occr in actual texts. Since the tagger we are developing is based on the possibility of recognising words by the help of a lexicon, it is of great importance to have a module that recognises new compounds. According to Munthe (1972), 10.4 per cent of all words in running text are compounds. Any text sample will contain a greatnumber of compounds. This statistics is true even for small samples. I took an arbitrary 440-word article from the newspaper Aftenposten from September this year, Full penhet om passunion (Full openness on passport union), and I quickly counted 47 compounds. Many of them a

Janne Bondi Johannessen; Helge Hauglin

1996-01-01T23:59:59.000Z

302

METHOD OF RECOVERING URANIUM COMPOUNDS  

DOE Patents (OSTI)

S>The recovery of uranium compounds which have been adsorbed on anion exchange resins is discussed. The uranium and thorium-containing residues from monazite processed by alkali hydroxide are separated from solution, and leached with an alkali metal carbonate solution, whereby the uranium and thorium hydrorides are dissolved. The carbonate solution is then passed over an anion exchange resin causing the uranium to be adsorbed while the thorium remains in solution. The uranium may be recovered by contacting the uranium-holding resin with an aqueous ammonium carbonate solution whereby the uranium values are eluted from the resin and then heating the eluate whereby carbon dioxide and ammonia are given off, the pH value of the solution is lowered, and the uranium is precipitated.

Poirier, R.H.

1957-10-29T23:59:59.000Z

303

Volatile organic compound sensing devices  

DOE Patents (OSTI)

Apparatus employing vapochromic materials in the form of inorganic double complex salts which change color reversibly when exposed to volatile organic compound (VOC) vapors is adapted for VOC vapor detection, VOC aqueous matrix detection, and selective VOC vapor detection. The basic VOC vapochromic sensor is incorporated in various devices such as a ground probe sensor, a wristband sensor, a periodic sampling monitor, a soil/water penetrometer, an evaporative purge sensor, and various vacuum-based sensors which are particularly adapted for reversible/reusable detection, remote detection, continuous monitoring, or rapid screening of environmental remediation and waste management sites. The vapochromic sensor is used in combination with various fiber optic arrangements to provide a calibrated qualitative and/or quantitative indication of the presence of VOCs.

Lancaster, Gregory D. (Idaho Falls, ID); Moore, Glenn A. (Idaho Falls, ID); Stone, Mark L. (Idaho Falls, ID); Reagen, William K. (Stillwater, MN)

1995-01-01T23:59:59.000Z

304

Volatile organic compound sensing devices  

DOE Patents (OSTI)

Apparatus employing vapochromic materials in the form of inorganic double complex salts which change color reversibly when exposed to volatile organic compound (VOC) vapors is adapted for VOC vapor detection, VOC aqueous matrix detection, and selective VOC vapor detection. The basic VOC vapochromic sensor is incorporated in various devices such as a ground probe sensor, a wristband sensor, a periodic sampling monitor, a soil/water penetrometer, an evaporative purge sensor, and various vacuum-based sensors which are particularly adapted for reversible/reusable detection, remote detection, continuous monitoring, or rapid screening of environmental remediation and waste management sites. The vapochromic sensor is used in combination with various fiber optic arrangements to provide a calibrated qualitative and/or quantitative indication of the presence of VOCs. 15 figs.

Lancaster, G.D.; Moore, G.A.; Stone, M.L.; Reagen, W.K.

1995-08-29T23:59:59.000Z

305

Volatile organic compound sensing devices  

DOE Patents (OSTI)

Apparatus employing vapochromic materials in the form of inorganic double complex salts which change color reversibly when exposed to volatile organic compound (VOC) vapors is adapted for VOC vapor detection, VOC aqueous matrix detection, and selective VOC vapor detection. The basic VOC vapochromic sensor is incorporated in various devices such as a ground probe sensor, a wristband sensor, a periodic sampling monitor, a soil/water penetrometer, an evaporative purge sensor, and various vacuum-based sensors which are particularly adapted for reversible/reusable detection, remote detection, continuous monitoring, or rapid screening of environmental remediation and waste management sites. The vapochromic sensor is used in combination with various fiber optic arrangements to provide a calibrated qualitative and/or quantitative indication of the presence of VOCs.

Lancaster, G.D.; Moore, G.A.; Stone, M.L.; Regen, W.K.

1993-12-31T23:59:59.000Z

306

Postcombustion measures for cleaner solid fuels combustion: activated carbons for toxic pollutants removal from flue gases  

SciTech Connect

In this work the efficiency of postcombustion measures (i.e., activated carbon utilization) to achieve cleaner solid fuels combustion was evaluated. Thus, two commercial activated carbons (Calgon F400 and RWE active coke) were tested for removing toxic polluting compounds (Hg, PCBs, PCDD/Fs) from the gas phase. The effects of the pore structure and surface chemistry of the activated carbons tested were investigated, along with the sorption temperature and sulfur addition in carbon matrix. Experiments were realized in a bench-scale adsorption unit and in a commercial solid fuels-fired hot water boiler. The results showed that both activated carbons tested are suitable for the removal of toxic compounds (i.e., Hg, PCBs, PCDD/Fs) from the gas phase. Due to differences in Hg adsorptive capacity and adsorption rate, which are attributed to the diversified pore structure and surface chemistry of the activated carbons, RWE active coke is, presumably, more suitable for continuous Hg removal (i.e., activated carbon injection), while Calgon F400 is more suitable for batch one (packed column). For both activated carbons, Hg adsorption capacity was reduced with temperature increase, while it was enhanced by the presence of sulfur. Oxygen surface functional groups seem to be involved in Hg adsorption mechanism. Lactones are believed to act as potential active sites for mercury adsorption, while phenols may act as inhibitors. The removal of PCBs and PCDD/Fs from the gas phase seems not to be a problem for the activated carbons tested, regardless of their pore structure or surface chemistry. 61 refs., 23 figs., 8 tabs.

G. Skodras; I. Diamantopoulou; P. Natas; A. Palladas; G.P. Sakellaropoulos [Aristotle University of Thessaloniki, Thessaloniki (Greece). Chemical Process Engineering Laboratory, Department of Chemical Engineering

2005-12-01T23:59:59.000Z

307

SULFUR REMOVAL FROM PIPE LINE NATURAL GAS FUEL: APPLICATION TO FUEL CELL POWER GENERATION SYSTEMS  

DOE Green Energy (OSTI)

Pipeline natural gas is being considered as the fuel of choice for utilization in fuel cell-based distributed generation systems because of its abundant supply and the existing supply infrastructure (1). For effective utilization in fuel cells, pipeline gas requires efficient removal of sulfur impurities (naturally occurring sulfur compounds or sulfur bearing odorants) to prevent the electrical performance degradation of the fuel cell system. Sulfur odorants such as thiols and sulfides are added to pipeline natural gas and to LPG to ensure safe handling during transportation and utilization. The odorants allow the detection of minute gas line leaks, thereby minimizing the potential for explosions or fires.

King, David L.; Birnbaum, Jerome C.; Singh, Prabhakar

2003-11-21T23:59:59.000Z

308

BIODESULF(TM), A Novel Biological Technology for the Removal of H2S From Sour Natural Gas  

Science Conference Proceedings (OSTI)

The state-of-the-art technologies for the removal of sulfur compounds from Sour Natural Gas (SNG) are not cost-effective when scaled down to approximately 2-5 MMSCFD. At the same time, the SNG Production is increasing at 3-6 TCF/Yr and -78 TCF potential reserves are also sour. Assuming only 3% treatment of this potential SNG market is for small volume processing, the potential U.S. Market is worth $0.14 to $0.28 billion. Therefore, the Gas Processing Industry is seeking novel, cost-effective, environmentally compatible and operator friendly technologies applicable to the small volume producers in the range of less than 1 MMSCFD to - 5 MMSCFD. A novel biological process, BIODESTJLFTM (patent pending), developed at ARCTECH removes H{sub 2}S and other sulfur contaminants that make the Natural Gas Sour. The removal is accomplished by utilizing an adapted mixed microbial culture (consortium). A variety of anaerobic microbial consortia from ARCTECH`s Microbial Culture Collection were grown and tested for removal of H{sub 2}S. One of these consortia, termed SS-11 was found to be particularly effective. Utilizing the SS-11 consortium, a process has been developed on a laboratory-scale to remove sulfur species from Sour Natural Gas at well head production pressures and temperatures. The process has been independently evaluated and found to be promising in effectively removing H{sub 2}S and other sulfur species cost effectively.

Srivastava, K.C.; Stashick, J.J.; Johnson, P.E.; Kaushik, N.K.

1997-10-01T23:59:59.000Z

309

Catalytic two-stage coal liquefaction process having improved nitrogen removal  

SciTech Connect

A process for catalytic multi-stage hydrogenation and liquefaction of coal to produce high yields of low-boiling hydrocarbon liquids containing low concentrations of nitogen compounds. First stage catalytic reaction conditions are 700.degree.-800.degree. F. temperature, 1500-3500 psig hydrogen partial pressure, with the space velocity maintained in a critical range of 10-40 lb coal/hr ft.sup.3 catalyst settled volume. The first stage catalyst has 0.3-1.2 cc/gm total pore volume with at least 25% of the pore volume in pores having diameters of 200-2000 Angstroms. Second stage reaction conditions are 760.degree.-870.degree. F. temperature with space velocity exceeding that in the first stage reactor, so as to achieve increased hydrogenation yield of low-boiling hydrocarbon liquid products having at least 75% removal of nitrogen compounds from the coal-derived liquid products.

Comolli, Alfred G. (Yardley, PA)

1991-01-01T23:59:59.000Z

310

Reactivity of target compounds for chemical coal desulfurization. Technical report, March 1, 1994--May 31, 1994  

SciTech Connect

This project seeks to identify representative organosulfur compounds which are removed by known coal desulfurization reactions. Demineralized coals are solvent extracted and the extracts fractionated to concentrate organosulfur compounds for analysis by Gas Chromatography/Mass Spectroscopy. After sulfur compounds are characterized, the parent extracts are subjected to reactions previously shown to reduce the organic sulfur content of Illinois coals, fractionated and again analyzed for organosulfur content to determine if the identified compounds reacted during the chemical treatment. The original coal also will be subjected to chemical desulfurization, extraction, fractionation and analysis in order to correlate changes in organic sulfur content of the coal with reactions of specific sulfur compounds. These compounds can thus be reliably considered as target molecules for the next generation of desulfurization processes. Work during this quarter has shown that fractionation and chromatography of pyridine extracts to isolate suitable samples for GC/MS analysis, although time-consuming, appears to be better than direct toluene extraction in terms of providing a representative set of compounds for analysis. The toluene soluble fractions prepared by this route contain aromatic sulfur compounds and O, N, S-containing hetrocycles. A set of these compounds has been identified and their fate following desulfurization of the parent coal extracts is under investigation. Previously studied desulfurization reactions using the single electron transfer reagent, K/THF/naphthalene, and the reactive nickel boride reagent have been repeated and analyzed by GC/MS. SET and nickel boride reactions of the THF soluble portions of pyridine coal are currently in progress.

Buchanan, D.H.; Amin, M.; Cunningham, R.; Galyen, J.; Ho, K.K.

1994-09-01T23:59:59.000Z

311

Process for selected gas oxide removal by radiofrequency catalysts  

DOE Patents (OSTI)

This process to remove gas oxides from flue gas utilizes adsorption on a char bed subsequently followed by radiofrequency catalysis enhancing such removal through selected reactions. Common gas oxides include SO.sub.2 and NO.sub.x.

Cha, Chang Y. (3807 Reynolds St., Laramie, WY 82070)

1993-01-01T23:59:59.000Z

312

Process for removing technetium from iron and other metals  

DOE Patents (OSTI)

A process for removing technetium from iron and other metals comprises the steps of converting the molten, alloyed technetium to a sulfide dissolved in manganese sulfide, and removing the sulfide from the molten metal as a slag. 4 figs.

Leitnaker, J.M.; Trowbridge, L.D.

1999-03-23T23:59:59.000Z

313

Process for removing technetium from iron and other metals  

DOE Patents (OSTI)

A process for removing technetium from iron and other metals comprises the steps of converting the molten, alloyed technetium to a sulfide dissolved in manganese sulfide, and removing the sulfide from the molten metal as a slag.

Leitnaker, James M. (Kingston, TN); Trowbridge, Lee D. (Oak Ridge, TN)

1999-01-01T23:59:59.000Z

314

Removing nuclear waste, one shipment at a time  

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

Stories Removing nuclear waste, one shipment at a time Removing nuclear waste, one shipment at a time The Lab's 1,000th shipment of transuranic waste recently left Los Alamos,...

315

DOE removes all remaining HEU from Hungary | National Nuclear...  

National Nuclear Security Administration (NNSA)

NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > NNSA Blog > DOE removes all remaining HEU from Hungary DOE removes all remaining HEU...

316

Method for removal of methane from coalbeds  

DOE Patents (OSTI)

A method for removing methane gas from underground coalbeds prior to mining the coal which comprises drilling at least one borehole from the surface into the coalbed. The borehole is started at a slant rather than directly vertically, and as it descends, a gradual curve is followed until a horizontal position is reached where the desired portion of the coalbed is intersected. Approaching the coalbed in this manner and fracturing the coalbed in the major natural fraction direction cause release of large amounts of the trapped methane gas.

Pasini, III, Joseph (Morgantown, WV); Overbey, Jr., William K. (Morgantown, WV)

1976-01-01T23:59:59.000Z

317

Compound cryopump for fusion reactors  

E-Print Network (OSTI)

We reconsider an old idea: a three-stage compound cryopump for use in fusion reactors such as DEMO. The helium "ash" is adsorbed on a 4.5 K charcoal-coated surface, while deuterium and tritium are adsorbed at 15-22 K on a second charcoal-coated surface. The helium is released by raising the first surface to ~30 K. In a separate regeneration step, deuterium and tritium are released at ~110 K. In this way, the helium can be pre-separated from other species. In the simplest design, all three stages are in the same vessel, with a single valve to close the pump off from the tokamak during regeneration. In an alternative design, the three stages are in separate vessels, connected by valves, allowing the stages to regenerate without interfering with each other. The inclusion of the intermediate stage would not affect the overall pumping speed significantly. The downstream exhaust processing system could be scaled down, as much of the deuterium and tritium could be returned directly to the reactor. This could reduce ...

Kovari, M; Shephard, T

2013-01-01T23:59:59.000Z

318

Method for etching thin films of niobium and niobium-containing compounds for preparing superconductive circuits  

DOE Green Energy (OSTI)

An improved method of preparing thin film superconducting electrical circuits of niobium or niobium compounds in which a thin film of the niobium or niobium compound is applied to a nonconductive substrate, and covered with a layer of photosensitive material. The sensitive material is in turn covered with a circuit pattern exposed and developed to form a mask of the circuit in photoresistive material on the surface of the film. The unmasked excess niobium film is removed by contacting the substrate with an aqueous etching solution of nitric acid, sulfuric acid and hydrogen fluoride, which will rapidly etch the niobium compound without undercutting the photoresist. A modification of the etching solution will permit thin films to be lifted from the substrate without further etching.

Kampwirth, Robert T. (Darien, IL); Schuller, Ivan K. (Woodridge, IL); Falco, Charles M. (Woodridge, IL)

1981-01-01T23:59:59.000Z

319

Development of new sorbents to remove mercury and selenium from flue gas. Final report, September 1, 1993--August 31, 1994  

Science Conference Proceedings (OSTI)

Mercury (Hg) and selenium (Se) are two of the volatile trace metals in coal, which are often not captured by conventional gas clean up devices of coal-fired boilers. An alternative is to use sorbents to capture the volatile components of trace metals after coal combustion. In this project sorbent screening tests were performed in which ten sorbents were selected to remove metallic mercury in N{sub 2}. These sorbents included activated carbon, char prepared from Ohio No. 5 coal, molecular sieves, silica gel, aluminum oxide, hydrated lime, Wyoming bentonite, kaolin, and Amberite IR-120 (an ion-exchanger). The sorbents were selected based on published information and B&W`s experience on mercury removal. The promising sorbent was then selected and modified for detailed studies of removal of mercury and selenium compounds. The sorbents were tested in a bench-scale adsorption facility. A known amount of each sorbent was loaded in the column as a packed bed. A carrier gas was bubbled through the mercury and selenium compounds. The vaporized species were carried by the gas and went through the sorbent beds. The amount of mercury and selenium compounds captured by the sorbents was determined by atomic absorption. Results are discussed.

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

1995-02-01T23:59:59.000Z

320

Removal of Fluoride from Waste Water of Aluminium Smelter by ...  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, 2011 TMS Annual Meeting & Exhibition. Symposium , General Abstracts: Light Metals Division. Presentation Title, Removal of ...

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Method for removing fluoride contamination from nitric acid  

DOE Patents (OSTI)

Fluoride ions are removed from nitric acid solution by contacting the vaporized solution with alumina or zirconium.

Pruett, David J. (Knoxville, TN); Howerton, William B. (Kingston, TN)

1982-01-01T23:59:59.000Z

322

Removing Pollutants from Water, Solar Energy - Programmaster.org  

Science Conference Proceedings (OSTI)

Aug 5, 2013 ... B. Materials for the Environment: Removing Pollutants from Water, Solar Energy Program Organizers: Fernand Marquis, Naval Postgraduate ...

323

Powder Removal from Complex Structures Produced Using Electron ...  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, Materials Science & Technology 2011. Symposium, Additive Manufacturing of Metals. Presentation Title, Powder Removal from ...

324

GTRI's Nuclear and Radiological Material Removal | National Nuclear...  

National Nuclear Security Administration (NNSA)

Removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our...

325

Removal of Inclusions from Solar Grade Silicon Using ...  

Science Conference Proceedings (OSTI)

Polysilicon in Photovoltaics: Market Conditions & Competing PV Technologies ... Removal of Inclusions from Solar Grade Silicon Using Electromagnetic Field.

326

Modified Bayer Process for Alumina Removal from Hanford Waste  

AREVA NC Inc. Modified Bayer Process for Alumina Removal from Hanford Waste January 24, 2007 Don Geniesse AREVA NC Inc.

327

Reading Comprehension - Dissecting and Compound Microscopes  

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

Dissecting and Compound Microscopes Two types of microscopes. _________ Dissecting and Compound Microscopes Two types of microscopes. _________ Dissecting Microscope Compound Microscope _________ eyepiece focus knob light light switch objective stage _________ eyepiece focus knob light light switch objective stage _________ eyepiece focus knob light light switch objective stage _________ eyepiece focus knob light light switch objective stage _________ eyepiece focus knob light light switch objective stage _________ eyepiece focus knob light light switch objective stage _________ Dissecting Microscope Compound Microscope _________ eyepieces focus knob light light switch objective stage _________ eyepieces focus knob light light switch objective stage _________ eyepieces focus knob light light switch objective stage _________ eyepieces focus knob light

328

Volatile organic compound emissions from composting.  

E-Print Network (OSTI)

??This paper is a review of the aerobic composting process and the emissions of volatile organic compounds (VOCs) from this process. To understand why and… (more)

Harris, Stephanie Rose Renée

2013-01-01T23:59:59.000Z

329

Modern Records of Radiatively Important Halogenated Compounds...  

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

at CDIAC sites: Methane, Nonmethane Hydrocarbons, Alkyl Nitrates, and Chlorinated Carbon Compounds including three Chlorofluorocarbons (CFC-11, CFC-12, and CFC-113) in...

330

Hydrodesulfurization catalysis by Chevrel phase compounds  

DOE Patents (OSTI)

A process is disclosed for the hydrodesulfurization of sulfur-containing hydrocarbon fuel with reduced ternary molybdenum sulfides, known as Chevrel phase compounds. Chevrel phase compounds of the general composition M.sub.x Mo.sub.6 S.sub.8, with M being Ho, Pb, Sn, Ag, In, Cu, Fe, Ni, or Co, were found to have hydrodesulfurization activities comparable to model unpromoted and cobalt-promoted MoS.sub.2 catalysts. The most active catalysts were the "large" cation compounds (Ho, Pb, Sn), and the least active catalysts were the "small" cation compounds (Cu, Fe, Ni, Co.).

McCarty, Kevin F. (Livermore, CA); Schrader, Glenn L. (Ames, IA)

1985-12-24T23:59:59.000Z

331

Why Sequence Bacteria That Reduce Sulfur Compounds?  

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

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

332

PLUTONIUM COMPOUNDS AND PROCESS FOR THEIR PREPARATION  

DOE Patents (OSTI)

This patent relates to certain new compounds of plutonium, and to the utilization of these compounds to effect purification or separation of the plutonium. The compounds are organic chelate compounds consisting of tetravalent plutonium together with a di(salicylal) alkylenediimine. These chelates are soluble in various organic solvents, but not in water. Use is made of this property in extracting the plutonium by contacting an aqueous solution thereof with an organic solution of the diimine. The plutonium is chelated, extracted and effectively separated from any impurities accompaying it in the aqueous phase.

Wolter, F.J.; Diehl, H.C. Jr.

1958-01-01T23:59:59.000Z

333

Process for synthesizing compounds from elemental powders  

DOE Patents (OSTI)

A process for synthesizing intermetallic compounds from elemental powders. The elemental powders are initially combined in ratio a which approximates the stoichiometric composition of the intermetallic compound. The mixed powders are then formed into a compact which is heat treated at a controlled rate of heating such that an exothermic reaction between the elements is initiated. The heat treatment may be performed under controlled conditions ranging from a vacuum (pressureless sintering) to compression (hot pressing) to produce a desired densification of the intermetallic compound. In a preferred form of the invention, elemental powders of Fe and Al are combined to form aluminide compounds of Fe{sub 3}Al and FeAl.

Rabin, B.H.; Wright, R.N.

1990-01-01T23:59:59.000Z

334

Process for removing polychlorinated biphenyls from soil  

DOE Patents (OSTI)

The present invention relates to a method of removing polychlorinated biphenyls from soil. The polychlorinated biphenyls are extracted from the soil by employing a liquid organic solvent dispersed in water in the ratio of about 1:3 to 3:1. The organic solvent includes such materials as short-chain hydrocarbons including kerosene or gasoline which are immiscible with water and are nonpolar. The organic solvent has a greater affinity for the PCB's than the soil so as to extract the PCB's from the soil upon contact. The organic solvent phase is separated from the suspended soil and water phase and distilled for permitting the recycle of the organic solvent phase and the concentration of the PCB's in the remaining organic phase. The present process can be satisfactorily practiced with soil containing 10 to 20% petroleum-based oils and organic fluids such as used in transformers and cutting fluids, coolants and the like which contain PCB's. The subject method provides for the removal of a sufficient concentration of PCB's from the soil to provide the soil with a level of PCB's within the guidelines of the Environmental Protection Agency.

Hancher, C.W.; Saunders, M.B.; Googin, J.M.

1984-11-16T23:59:59.000Z

335

TYPE A VERIFICATION FOR THE HIGH FLUX BEAM REACTOR UNDERGROUND UTILITIES REMOVAL PHASE 2 DF WASTE LINE REMOVAL, BNL  

SciTech Connect

5098-SR-02-0 PROJECT-SPECIFIC TYPE A VERIFICATION FOR THE HIGH FLUX BEAM REACTOR UNDERGROUND UTILITIES REMOVAL PHASE 2 DF WASTE LINE REMOVAL, BROOKHAVEN NATIONAL LABORATORY

P.C. Weaver

2010-07-09T23:59:59.000Z

336

Alloys and Compounds for Thermoelectric and Solar Cell Applications  

Science Conference Proceedings (OSTI)

Alloys and Compounds for Thermoelectric and Solar Cell Applications II: Alloys and Compounds for Thermoelectric and Solar Cell Applications: Thermoelectric ...

337

Massive Hanford Test Reactor Removed- Plutonium Recycle Test Reactor removed from Hanford’s 300 Area  

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

RICHLAND, WA – Hanford’s River Corridor contractor, Washington Closure Hanford, has met a significant cleanup challenge on the U.S. Department of Energy’s (DOE) Hanford Site by removing a 1,082-ton nuclear test reactor from the 300 Area.

338

Hanford Deep Dig Removes Contaminated Soil | Department of Energy  

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

Hanford Deep Dig Removes Contaminated Soil Hanford Deep Dig Removes Contaminated Soil Hanford Deep Dig Removes Contaminated Soil March 11, 2013 - 12:00pm Addthis An aerial view of Hanford’s D Area shows the D Reactor (lower left) and DR Reactor. Workers are digging 85 feet to groundwater at two sites there to remove chromium contamination. An aerial view of Hanford's D Area shows the D Reactor (lower left) and DR Reactor. Workers are digging 85 feet to groundwater at two sites there to remove chromium contamination. Workers remove soil contaminated with sodium dichromate to prevent the chemical from reaching the groundwater and eventually the Columbia River. Workers remove soil contaminated with sodium dichromate to prevent the chemical from reaching the groundwater and eventually the Columbia River.

339

Hanford Deep Dig Removes Contaminated Soil | Department of Energy  

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

Deep Dig Removes Contaminated Soil Deep Dig Removes Contaminated Soil Hanford Deep Dig Removes Contaminated Soil March 11, 2013 - 12:00pm Addthis An aerial view of Hanford’s D Area shows the D Reactor (lower left) and DR Reactor. Workers are digging 85 feet to groundwater at two sites there to remove chromium contamination. An aerial view of Hanford's D Area shows the D Reactor (lower left) and DR Reactor. Workers are digging 85 feet to groundwater at two sites there to remove chromium contamination. Workers remove soil contaminated with sodium dichromate to prevent the chemical from reaching the groundwater and eventually the Columbia River. Workers remove soil contaminated with sodium dichromate to prevent the chemical from reaching the groundwater and eventually the Columbia River.

340

EM Employs Innovative Technology to Remove Radioactive Sludge | Department  

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

Employs Innovative Technology to Remove Radioactive Sludge Employs Innovative Technology to Remove Radioactive Sludge EM Employs Innovative Technology to Remove Radioactive Sludge September 1, 2012 - 12:00pm Addthis Testing and equipment simulations ensure first-of-a-kind technological processes for sludge removal can be conducted safely and efficiently. Testing and equipment simulations ensure first-of-a-kind technological processes for sludge removal can be conducted safely and efficiently. RICHLAND, Wash. - The Richland Operations Office and contractor CH2M HILL Plateau Remediation Company successfully removed a portion of a highly radioactive sludge from underwater storage in a large basin adjacent to the K West reactor at the Hanford site this month. In that milestone, workers removed sludge originating from knock-out pots,

Note: This page contains sample records for the topic "removing asphalt compounds" 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

NETL: Gasification Systems - Warm Gas Multi-Contaminant Removal System  

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

Warm Gas Multi-Contaminant Removal System Warm Gas Multi-Contaminant Removal System Project Number: DE-SC00008243 TDA Research, Inc. is developing a high-capacity, low-cost sorbent that removes anhydrous ammonia (NH3), mercury (Hg), and trace contaminants from coal- and coal/biomass-derived syngas. The clean-up system will be used after the bulk warm gas sulfur removal step, and remove NH3 and Hg in a regenerable manner while irreversibly capturing all other trace metals (e.g., Arsenic, Selenium) reducing their concentrations to sub parts per million (ppm) levels. Current project plans include identifying optimum chemical composition and structure that provide the best sorbent performance for removing trace contaminants, determining the effect of operating parameters, conducting multiple-cycle experiments to test the life of the sorbent for NH3 and Hg removal, and conducting a preliminary design of the sorbent reactor.

342

On Quantum Capacity of Compound Channels  

E-Print Network (OSTI)

In this paper we address the issue of universal or robust communication over quantum channels. Specifically, we consider memoryless communication scenario with channel uncertainty which is an analog of compound channel in classical information theory. We determine the quantum capacity of finite compound channels and arbitrary compound channels with informed decoder. Our approach in the finite case is based on the observation that perfect channel knowledge at the decoder does not increase the capacity of finite quantum compound channels. As a consequence we obtain coding theorem for finite quantum averaged channels, the simplest class of channels with long-term memory. The extension of these results to quantum compound channels with uninformed encoder and decoder, and infinitely many constituents remains an open problem.

I. Bjelakovic; H. Boche; J. Noetzel

2008-08-07T23:59:59.000Z

343

Tritium removal and separation technology developments  

Science Conference Proceedings (OSTI)

Recent increased interest from regulators and the public has led more organizations to consider the environmental impact and safety considerations of tritium handling. Examples include the significance of the tritium isotope separation system on ITER licensing, remediation of ground water from power utilities and government facilities and concerns of high tritium concentrations within operational CANDU reactors. GE Healthcare, formerly Amersham pic, has been producing tritium-labelled chemicals since the late 1940's. GE's manufacturing site located near Cardiff, UK has installed a tritium waste treatment and enrichment facility to radically reduce tritium discharges to the environment. This facility employs a continuous processing plant that recovers tritium from a complex mixture of tritiated organic and aqueous waste compounds. Two isotope separation techniques are used to achieve a final pure tritium product, which is used in the manufacturing of labelled compounds. Building upon this experience, together with Special Separations Applications Inc. (SSAI), GE has developed a large-scale diffusion-based isotope separation process as an alternative to conventional cryogenic distillation. Having a tritium inventory an order of magnitude lower than conventional cryogenic distillation, this process is attractive for heavy water detritiation, applicable to single and multi-unit CANDU reactors and research reactors as well as fusion applications. Additionally, the new process has advantages of being cryogen-free, less complex, simple to operate and having improved conventional and radiological safety. (authors)

Bonnett, I. [General Electric, Hitachi Nuclear Energy Canada Inc., 1160 Monaghan Rd, Peterborough, ON K9J 7B5 (Canada); Busigin, A. [Special Separations Applications, Inc., 55 Water Street East, Brockville, ON K6V 1A3 (Canada); Shapiro, A. [General Electric GE, Global Research Center, 1 Research Circle, Niskayuna, NY 12309 (United States)

2008-07-15T23:59:59.000Z

344

Categorical Exclusion 4566, Ash Removal Project  

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

FOrnI FOrnI Project Title: Ash Removal Project (4566) Program or Program Office: Y -12 Site Office Location: Oak Ridge Tennessee Project Description: This work scope is to split, containerize, package, transport and disposition one hundred and two (102) cans of mixed waste. General Administration/Management OA I - Routine business actions OA2 * Administrative contract amendments OA4 - Interpretations/rulings for existing regulations OA5 - Regulatory interpretations without environmental effect OA6 - Procedural rule makings upgrade OA 7 - Transfer of property, use unchanged OA8 . Award of technical supportlM&O/personal service contracts OA9 - Info gathering, analysis, documentation, dissemination, and training OA 10 - Reports on non-DOE legislation OA II -

345

AX Tank Farm tank removal study  

SciTech Connect

This report considers the feasibility of exposing, demolishing, and removing underground storage tanks from the 241-AX Tank Farm at the Hanford Site. For the study, it was assumed that the tanks would each contain 360 ft{sup 3} of residual waste (corresponding to the one percent residual Inventory target cited in the Tri-Party Agreement) at the time of demolition. The 241-AX Tank Farm is being employed as a ''strawman'' in engineering studies evaluating clean and landfill closure options for Hanford single-shell tank farms. The report is one of several reports being prepared for use by the Hanford Tanks Initiative Project to explore potential closure options and to develop retrieval performance evaluation criteria for tank farms.

SKELLY, W.A.

1998-10-14T23:59:59.000Z

346

Electrochemical removal of material from metallic work  

DOE Patents (OSTI)

Deburring, polishing, surface forming and the like are carried out by electrochemical machining with conformable electrode means including an electrically conducting and an insulating web. The surface of the work to be processed is covered by a deformable electrically insulating web or cloth which is perforated and conforms with the work. The web is covered by a deformable perforated electrically conducting screen electrode which also conforms with, and is insulated from, the work by the insulating web. An electrolyte is conducted through the electrode and insulating web and along the work through a perforated elastic member which engages the electrode under pressure pressing the electrode and web against the work. High current under low voltage is conducted betwen the electrode and work through the insulator, removing material from the work. Under the pressure of the elastic member, the electrode and insulator continue to conform with the work and the spacing between the electrode and work is maintained constant.

Csakvary, Tibor (Wilkens Township, Allegheny County, PA); Fromson, Robert E. (Wilkens Township, Allegheny County, PA)

1980-05-13T23:59:59.000Z

347

The HMDS Coating Flaw Removal Tool  

Science Conference Proceedings (OSTI)

In many high energy laser systems, optics with HMDS sol gel antireflective coatings are placed in close proximity to each other making them particularly susceptible to certain types of strong optical interactions. During the coating process, halo shaped coating flaws develop around surface digs and particles. Depending on the shape and size of the flaw, the extent of laser light intensity modulation and consequent probability of damaging downstream optics may increase significantly. To prevent these defects from causing damage, a coating flaw removal tool was developed that deploys a spot of decane with a syringe and dissolves away the coating flaw. The residual liquid is evacuated leaving an uncoated circular spot approximately 1mm in diameter. The resulting uncoated region causes little light intensity modulation and thus has a low probability of causing damage in optics downstream from the mitigated flaw site.

Monticelli, M V; Nostrand, M C; Mehta, N; Kegelmeyer, L; Johnson, M A; Fair, J; Widmayer, C

2008-10-24T23:59:59.000Z

348

AX Tank Farm tank removal study  

Science Conference Proceedings (OSTI)

This report examines the feasibility of remediating ancillary equipment associated with the 241-AX Tank Farm at the Hanford Site. Ancillary equipment includes surface structures and equipment, process waste piping, ventilation components, wells, and pits, boxes, sumps, and tanks used to make waste transfers to/from the AX tanks and adjoining tank farms. Two remedial alternatives are considered: (1) excavation and removal of all ancillary equipment items, and (2) in-situ stabilization by grout filling, the 241-AX Tank Farm is being employed as a strawman in engineering studies evaluating clean and landfill closure options for Hanford single-shell tanks. This is one of several reports being prepared for use by the Hanford Tanks Initiative Project to explore potential closure options and to develop retrieval performance evaluation criteria for tank farms.

SKELLY, W.A.

1999-02-24T23:59:59.000Z

349

Effect of sequential removal of organic matter on the surface morphology of humin  

SciTech Connect

Natural organic matter in soils interacts with surfaces of inorganic materials, primarily aluminosilicates or clay minerals, to form a strongly associated organo-mineral composite known as humin. Because of humin`s insolubility, it is recognized as the primary sorbent of many anthropogenic organic compounds (AOCs) introduced into soil systems. This recognition has significant implications for understanding the fate and transport of AOCs, the effective remediation of contaminated sites, and the formulation and application of various agrochemicals. Humin was isolated from four soil samples. Surface area, surface charge, porosity measurements, and fractal analysis of small-angle X-ray scattering data were used to characterize changes in the surface properties resulting from selective removal of the various components of organic matter from humin. Organic matter was removed selectively from humin by Soxhlet extraction, disaggregation with the methylisobutylketone (MIBK) method, and bromine oxidation. The surface fractal dimensions decreased while surface area increased, and surface pore size decreased upon removal of organic matter. These results suggest that the mineral components of humin have smooth surfaces over length scales of {approximately}1 to 15 run, and that it is the organic matter coatings that are responsible for their surface roughness. The surfaces of all the components of humin were found to be dominated by micro and mesopores that could be responsible for humin`s high sorptive uptake of organic chemicals.

Malekani, K.; Rice, J.A. [South Dakota State Univ., Brookings, SD (United States)] [South Dakota State Univ., Brookings, SD (United States); Lin, Jar-Shyong [Oak Ridge National Lab., TN (United States)] [Oak Ridge National Lab., TN (United States)

1997-05-01T23:59:59.000Z

350

Comparison of NOx Removal Efficiencies in Compost Based Biofilters Using Four Different Compost Sources  

Science Conference Proceedings (OSTI)

In 1998, 3.6 trillion kilowatt-hours of electricity were generated in the United States. Over half of this was from coal-fired power plants, resulting in more than 8.3 million tons of nitrogen oxide (NOx) compounds being released into the environment. Over 95% of the NOx compounds produced during coal combustion are in the form of nitric oxide (NO). NOx emission regulations are becoming increasingly stringent, leading to the need for new, cost effective NOx treatment technologies. Biofiltration is such a technology. NO removal efficiencies were compared in compost based biofilters using four different composts. In previous experiments, removal efficiencies were typically highest at the beginning of the experiment, and decreased as the experiments proceeded. This work tested different types of compost in an effort to find a compost that could maintain NO removal efficiencies comparable to those seen early in the previous experiments. One of the composts was wood based with manure, two were wood based with high nitrogen content sludge, and one was dairy compost. The wood based with manure and one of the wood based with sludge composts were taken directly from an active compost pile while the other two composts were received in retail packaging which had been out of active piles for an indeterminate amount of time. A high temperature (55-60°C) off-gas stream was treated in biofilters operated under denitrifying conditions. Biofilters were operated at an empty bed residence time of 13 seconds with target inlet NO concentrations of 500 ppmv. Lactate was the carbon and energy source. Compost was sampled at 10-day intervals to determine aerobic and anaerobic microbial densities. Compost was mixed at a 1:1 ratio with lava rock and calcite was added at 100g/kg of compost. In each compost tested, the highest removal efficiencies occurred within the first 10 days of the experiment. The wood based with manure peaked at day 3 (77.14%), the dairy compost at day 1 (80.74%), the active wood based with sludge at day 5 (68.15%) and the inactive wood based with sludge at day 9 (63.64%, this compost was frozen when received). These levels gradually decreased throughout the remainder of the experiment until they fell between 40% and 60%. Decreasing removal efficiency was characteristic of all the composts tested, regardless of their makeup or activity state prior to testing. Although microbial densities and composition between composts may have differed, there was little change in densities within each experiment.

Lacey, Jeffrey Alan; Lee, Brady Douglas; Apel, William Arnold

2001-06-01T23:59:59.000Z

351

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Europium Intermetallic Compounds Print Towards Heavy Fermions in Europium Intermetallic Compounds Print For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

352

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Europium Intermetallic Compounds Print Towards Heavy Fermions in Europium Intermetallic Compounds Print For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

353

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Towards Heavy Fermions in Europium Intermetallic Compounds Towards Heavy Fermions in Europium Intermetallic Compounds Print Wednesday, 29 July 2009 00:00 For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

354

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Europium Intermetallic Compounds Print Towards Heavy Fermions in Europium Intermetallic Compounds Print For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

355

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Europium Intermetallic Compounds Print Towards Heavy Fermions in Europium Intermetallic Compounds Print For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

356

Towards Heavy Fermions in Europium Intermetallic Compounds  

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

Towards Heavy Fermions in Europium Intermetallic Compounds Print Towards Heavy Fermions in Europium Intermetallic Compounds Print For decades, intermetallic compounds of rare-earth metals have been favorite systems of the research community studying strong electron correlations in solids. Nowadays rare-earth intermetallics are often treated as model systems for studies of zero-temperature quantum critical phase transitions, since heavy-fermion rare-earth compounds (in which the electron effective mass is orders of magnitude larger than the bare electron mass) have provided the clearest evidence for these continuous phase transitions, which are controlled by such parameters as chemical composition, magnetic field, and pressure, rather than temperature. A new study of a europium-based compound by an international team led by researchers from the Technische Universität Dresden in Germany hints that this compound could join well-known compounds of cerium, ytterbium, and uranium as a new material suitable for research on quantum critical transitions. This finding is exciting, since physicists hope that the use of a new material will give an additional degree of freedom for researching quantum critical behavior.

357

--No Title--  

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

Remove the existing asphalt pavement within the On-Dock Rail Straddle Portal Test Facility project area and install the proposed Roller Compacted Concrete (RCC) pavement. Revision...

358

Metal Cutting for Large Component Removal  

Science Conference Proceedings (OSTI)

Decommissioning of commercial nuclear power plants presents technological challenges. One major challenge is the removal of large components mainly consisting of the reactor vessel, steam generators and pressurizer. In order to remove and package these large components nozzles must be cut from the reactor vessel to precise tolerances. In some cases steam generators must be segmented for size and weight reduction. One innovative technology that has been used successfully at several commercial nuclear plant decommissioning is diamond wire sawing. Diamond wire sawing is performed by rotating a cable with diamond segments attached using a flywheel approximately 24 inches in diameter driven remotely by a hydraulic pump. Tension is provided using a gear rack drive which also takes up the slack in the wire. The wire is guided through the use of pulleys keeps the wire in a precise location. The diamond wire consists of 1/4 inch aircraft cable with diamond beads strung over the cable separated by springs and brass crimps. Standard wire contains 40 diamond beads per meter and can be made to any length. Cooling the wire and controlling the spread of contamination presents significant challenges. Under normal circumstances the wire is cooled and the cutting kerf cleaned by using water. In some cases of reactor nozzle cuts the use of water is prohibited because it cannot be controlled. This challenge was solved by using liquid Carbon Dioxide as the cooling agent. The liquid CO{sub 2} is passed through a special nozzle which atomizes the liquid into snowflakes which is introduced under pressure to the wire. The snowflakes attach to the wire keeping it cool and to the metal shavings. As the CO{sub 2} and metal shavings are released from the wire due to its fast rotation, the snowflakes evaporate leaving only the fine metal shavings as waste. Secondary waste produced is simply the small volume of fine metal shavings removed from the cut surface. Diamond wire sawing using CO{sub 2} cooling has been employed for cutting the reactor nozzles at San Onofre Unit 1 and at Connecticut Yankee. These carbon steel nozzles ranged up to 54 inch diameter with a 15 inch thick wall and an interior stainless cladding. Diamond wire sawing using traditional water cooling has been used to segment the reactor head at Rancho Seco and for cutting reactor nozzles and control rod drive tubes at Dairyland Power's Lacrosse BWR project. Advantages: - ALARA: All cutting is preformed remotely significantly reducing dose. Stringing of wires is accomplished using long handle tools. - Secondary waste is reduced to just the volume of material cut with the diamond wire. - The potential for airborne contamination is eliminated. Due to the flexibility of the wire, any access restrictions and interferences can be accommodated using pulleys and long handle tools. - The operation is quiet. Disadvantages: - With Liquid Carbon Dioxide cooling and cleaning, delivery of the material must be carefully planned. The longer the distance from the source to the cut area, the greater the chance for pressure drop and subsequent problems with line freezing. - Proper shrouding and ventilation are required for environmental reasons. In each case, the metal structures were cut at a precise location. Radiation dose was reduced significantly by operating the equipment from a remote location. The cuts were very smooth and completed on schedule. Each project must be analyzed individually and take into account many factors including access, radiological conditions, environmental conditions, schedule requirements, packaging requirements and size of cuts.

Hulick, Robert M. [Bluegrass Concrete Cutting Inc., 107 Mildred Street PO Box 427, Greenville, Alabama 36037 (United States)

2008-01-15T23:59:59.000Z

359

ADVANCES IN HEXAVALENT CHROMIUM REMOVAL AT HANFORD  

SciTech Connect

At the Hanford Site, chromium was used as a corrosion inhibitor in the reactor cooling water and was introduced into the groundwater as a result of planned and unplanned discharges from reactors during plutonium production since 1944. Beginning in 1995, groundwater treatment methods were evaluated leading to the use of pump and treat facilities with ion exchange using Dowex 21 K, a regenerable strong base anion exchange resin. This required regeneration of the resin, which is currently performed offsite. Resin was installed in a 4 vessel train, with resin removal required from the lead vessel approximately once a month. In 2007, there were 8 trains (32 vessels) in operation. In 2008, DOE recognized that regulatory agreements would require significant expansion in the groundwater chromium treatment capacity. Previous experience from one of the DOE project managers led to identification of a possible alternative resin, and the contractor was requested to evaluate alternative resins for both cost and programmatic risk reductions. Testing was performed onsite in 2009 and 2010, using a variety of potential resins in two separate facilities with groundwater from specific remediation sites to demonstrate resin performance in the specific groundwater chemistry at each site. The testing demonstrated that a weak base anion single-use resin, ResinTech SIR-700, was effective at removing chromium, had a significantly higher capacity, could be disposed of efficiently on site, and would eliminate the complexities and programmatic risks from sampling, packaging, transportation and return of resin for regeneration. This resin was installed in Hanford's newest groundwater treatment facility, called 100-DX, which began operations in November, 2010, and used in a sister facility, 100-HX, which started up in September of 2011. This increased chromium treatment capacity to 25 trains (100 vessels). The resin is also being tested in existing facilities that utilize Dowex 21 K for conversion to the new resin. This paper will describe the results of the testing, performance in the facilities, continued optimization in the pump and treat facilities, and the estimated savings and non-tangible benefits of the conversion.

NESHEM DO; RIDDELLE J

2012-01-30T23:59:59.000Z

360

Evaluation of sustained release polylactate electron donors for removal of hexavalent chromium from contaminated groundwater  

DOE Green Energy (OSTI)

To evaluate the efficacy of bioimmobilization of Cr(VI) in groundwater at the Department of Energy Hanford site, we conducted a series of microcosm experiments using a range of commercial electron donors with varying degrees of lactate polymerization (polylactate). These experiments were conducted using Hanford Formation sediments (coarse sand and gravel) immersed in Hanford groundwater, which were amended with Cr(VI) and several types of lactate-based electron donors (Hydrogen Release Compound, HRC; primer-HRC, pHRC; extended release HRC) and the polylactate-cysteine form (Metal Remediation Compound, MRC). The results showed that polylactate compounds stimulated an increase in bacterial biomass and activity to a greater extent than sodium lactate when applied at equivalent carbon concentrations. At the same time, concentrations of headspace hydrogen and methane increased and correlated with changes in the microbial community structure. Enrichment of Pseudomonas spp. occurred with all lactate additions, and enrichment of sulfate-reducing Desulfosporosinus spp. occurred with almost complete sulfate reduction. The results of these experiments demonstrate that amendment with the pHRC and MRC forms result in effective removal of Cr(VI) from solution most likely by both direct (enzymatic) and indirect (microbially generated reductant) mechanisms.

Brodie, E.L.; Joyner, D. C.; Faybishenko, B.; Conrad, M. E.; Rios-Velazquez, C.; Mork, B.; Willet, A.; Koenigsberg, S.; Herman, D.; Firestone, M. K.; Hazen, T. C.; Malave, Josue; Martinez, Ramon

2011-02-15T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
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361

Oak Ridge Removes Laboratory's Greatest Source of Groundwater  

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

Oak Ridge Removes Laboratory's Greatest Source of Groundwater Oak Ridge Removes Laboratory's Greatest Source of Groundwater Contamination Oak Ridge Removes Laboratory's Greatest Source of Groundwater Contamination May 1, 2012 - 12:00pm Addthis Workers remove the 4,000-gallon Tank W-1A, which was ORNL’s greatest source of groundwater contamination. Workers remove the 4,000-gallon Tank W-1A, which was ORNL's greatest source of groundwater contamination. Workers load boxes containing contaminated soil that surrounded Tank W-1A. Workers load boxes containing contaminated soil that surrounded Tank W-1A. The 6,500-pound Tank W-1A is shipped away from ORNL. The 6,500-pound Tank W-1A is shipped away from ORNL. Workers remove the 4,000-gallon Tank W-1A, which was ORNL's greatest source of groundwater contamination. Workers load boxes containing contaminated soil that surrounded Tank W-1A.

362

Magnetic Process For Removing Heavy Metals From Water Employing Magnetites  

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

Magnetic Process For Removing Heavy Metals From Water Employing Magnetic Process For Removing Heavy Metals From Water Employing Magnetites Magnetic Process For Removing Heavy Metals From Water Employing Magnetites A process for removing heavy metals from water is provided. The process includes the steps of introducing magnetite to a quantity of water containing heavy metal. Available for thumbnail of Feynman Center (505) 665-9090 Email Magnetic Process For Removing Heavy Metals From Water Employing Magnetites A process for removing heavy metals from water is provided. The process includes the steps of introducing magnetite to a quantity of water containing heavy metal. The magnetite is mixed with the water such that at least a portion of, and preferably the majority of, the heavy metal in the water is bound to the magnetite. Once this occurs the magnetite and

363

Oak Ridge Removes Laboratory's Greatest Source of Groundwater  

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

Oak Ridge Removes Laboratory's Greatest Source of Groundwater Oak Ridge Removes Laboratory's Greatest Source of Groundwater Contamination Oak Ridge Removes Laboratory's Greatest Source of Groundwater Contamination May 1, 2012 - 12:00pm Addthis Workers remove the 4,000-gallon Tank W-1A, which was ORNL’s greatest source of groundwater contamination. Workers remove the 4,000-gallon Tank W-1A, which was ORNL's greatest source of groundwater contamination. Workers load boxes containing contaminated soil that surrounded Tank W-1A. Workers load boxes containing contaminated soil that surrounded Tank W-1A. The 6,500-pound Tank W-1A is shipped away from ORNL. The 6,500-pound Tank W-1A is shipped away from ORNL. Workers remove the 4,000-gallon Tank W-1A, which was ORNL's greatest source of groundwater contamination. Workers load boxes containing contaminated soil that surrounded Tank W-1A.

364

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

365

Compound and Elemental Analysis | Open Energy Information  

Open Energy Info (EERE)

Compound and Elemental Analysis Compound and Elemental Analysis Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Technique: Compound and Elemental Analysis Details Activities (104) Areas (69) Regions (6) NEPA(0) Exploration Technique Information Exploration Group: Lab Analysis Techniques Exploration Sub Group: Fluid Lab Analysis Parent Exploration Technique: Fluid Lab Analysis Information Provided by Technique Lithology: Stratigraphic/Structural: Hydrological: Results can aid in the determination of fluid source regions and circulation pathways. Thermal: Certain elements exhibit high spatial correlation with high-temperature geothermal systems. Cost Information Low-End Estimate (USD): 15.001,500 centUSD 0.015 kUSD 1.5e-5 MUSD 1.5e-8 TUSD / compound Median Estimate (USD): 30.003,000 centUSD

366

Fission Barriers of Compound Superheavy Nuclei  

E-Print Network (OSTI)

The dependence of fission barriers on the excitation energy of the compound nucleus impacts the survival probability of superheavy nuclei synthesized in heavy-ion fusion reactions. In this work, we investigate the isentropic ...

Sheikh, J. A.

367

Production method for making rare earth compounds  

DOE Patents (OSTI)

A method of making a rare earth compound, such as a earth-transition metal permanent magnet compound, without the need for producing rare earth metal as a process step, comprises carbothermically reacting a rare earth oxide to form a rare earth carbide and heating the rare earth carbide, a compound-forming reactant (e.g. a transition metal and optional boron), and a carbide-forming element (e.g. a refractory metal) that forms a carbide that is more thermodynamically favorable than the rare earth carbide whereby the rare earth compound (e.g. Nd.sub.2 Fe.sub.14 B or LaNi.sub.5) and a carbide of the carbide-forming element are formed.

McCallum, R. William (Ames, IA); Ellis, Timothy W. (Ames, IA); Dennis, Kevin W. (Ames, IA); Hofer, Robert J. (Ames, IA); Branagan, Daniel J. (Ames, IA)

1997-11-25T23:59:59.000Z

368

Insulating shade assembly with removable cover  

SciTech Connect

An insulating window shade assembly is described which consists of: bracket means adapted to be mounted on the frame of a window; a first roller carrying an insulating shade and being disposed within the bracket means on the inside of the window, the shade being adapted to be drawn from the roller to cover the inside of the window and to be wound upon the roller to expose the window, a second roller carrying a removable cover fabric on the inside of the shade and being supported by the bracket means, the second roller being spaced from and disposed independently of the first roller, means disposed adjacent only the bottom edge of the insulating shade for connecting only the bottom edge of the cover fabric to the bottom only of the insulating shade so that the insulating shade and cover fabric may be drawn together over the inside of the window; guide means disposed adjacent the second roller and between the second roller and the insulating shade, the cover fabric passing over the guide means, for causing the cover fabric to hang closely adjacent the front of the insulating shade when the insulating shade is drawn over the window and when the insulating shade and cover fabric are connected together by the connecting means, and means for continually tensioning the cover fabric when the insulating shade is drawn and when the cover fabric is connected thereto so that the cover fabric lies smoothly over the shade.

Hausmann, S.; McLane, A. Jr.

1986-09-09T23:59:59.000Z

369

Metagenomic analysis of phosphorus removing sludgecommunities  

SciTech Connect

Enhanced Biological Phosphorus Removal (EBPR) is not wellunderstood at the metabolic level despite being one of the best-studiedmicrobially-mediated industrial processes due to its ecological andeconomic relevance. Here we present a metagenomic analysis of twolab-scale EBPR sludges dominated by the uncultured bacterium, "CandidatusAccumulibacter phosphatis." This analysis resolves several controversiesin EBPR metabolic models and provides hypotheses explaining the dominanceof A. phosphatis in this habitat, its lifestyle outside EBPR and probablecultivation requirements. Comparison of the same species from differentEBPR sludges highlights recent evolutionary dynamics in the A. phosphatisgenome that could be linked to mechanisms for environmental adaptation.In spite of an apparent lack of phylogenetic overlap in the flankingcommunities of the two sludges studied, common functional themes werefound, at least one of them complementary to the inferred metabolism ofthe dominant organism. The present study provides a much-needed blueprintfor a systems-level understanding of EBPR and illustrates thatmetagenomics enables detailed, often novel, insights into evenwell-studied biological systems.

Garcia Martin, Hector; Ivanova, Natalia; Kunin, Victor; Warnecke,Falk; Barry, Kerrie; McHardy, Alice C.; Yeates, Christine; He, Shaomei; Salamov, Asaf; Szeto, Ernest; Dalin, Eileen; Putnam, Nik; Shapiro, HarrisJ.; Pangilinan, Jasmyn L.; Rigoutsos, Isidore; Kyrpides, Nikos C.; Blackall, Linda Louise; McMahon, Katherine D.; Hugenholtz, Philip

2006-02-01T23:59:59.000Z

370

Method of removing oxidized contaminants from water  

DOE Patents (OSTI)

The present invention is a method for removing oxidized contaminant(s) from water. More specifically, the invention has the steps of contacting water containing the oxidized contaminant(s) with a layered aluminosilicate having Fe(II). The aluminosilicate may contain naturally occurring Fe(II), or the Fe(II) may be produced by reducing Fe(III) that is initially present. Reduction may be either by exposure to a chemical or biological reductant. Contacting the water containing oxidized contaminant(s) may be by (1) injection of Fe(II)-containing layered aluminosilicate, via a well, into a saturated zone where it is likely to intercept the contaminated water; (2) injection of contaminated water into a vessel containing the Fe(II)-bearing layered aluminosilicate; and (3) first reducing Fe(III) in the layered aluminosilicate to Fe(II) by injection of a biological or chemical reductant, into an aquifer or vessel having sufficient Fe(III)-bearing aluminosilicate to produce the necessary Fe(II). 8 figs.

Amonette, J.E.; Fruchter, J.S.; Gorby, Y.A.; Cole, C.R.; Cantrell, K.J.; Kaplan, D.I.

1998-07-21T23:59:59.000Z

371

Method of removing oxidized contaminants from water  

DOE Patents (OSTI)

The present invention is a method for removing oxidized contaminant(s) from water. More specifically, the invention has the steps of contacting water containing the oxidized contaminant(s) with a layered aluminosilicate having Fe(II). The aluminosilicate may contain naturally occurring Fe(II), or the Fe(II) may be produced by reducing Fe(III) that is initially present. Reduction may be either by exposure to a chemical or biological reductant. Contacting the water containing oxidized contaminant(s) may be by (1) injection of Fe(II)-containing layered aluminosilicate, via a well, into a saturated zone where it is likely to intercept the contaminated water; (2) injection of contaminated water into a vessel containing the Fe(II)-bearing layered aluminosilicate; and (3) first reducing Fe(III) in the layered aluminosilicate to Fe(II) by injection of a biological or chemical reductant, into an aquifer or vessel having sufficient Fe(III)-bearing aluminosilicate to produce the necessary Fe(II).

Amonette, James E. (Richland, WA); Fruchter, Jonathan S. (Richland, WA); Gorby, Yuri A. (Richland, WA); Cole, Charles R. (West Richmond, WA); Cantrell, Kirk J. (West Richmond, WA); Kaplan, Daniel I. (Richland, WA)

1998-01-01T23:59:59.000Z

372

HIGH SO2 REMOVAL EFFICIENCY TESTING  

Science Conference Proceedings (OSTI)

This final report describes the results of performance tests at six full-scale wet lime- and limestone-reagent flue gas desulfurization (FGD) systems. The objective of these tests was to evaluate the effectiveness of low capital cost sulfur dioxide (SO{sub 2}) removal upgrades for existing FGD systems as an option for complying with the provisions of the Clean Air Act Amendments of 1990. The upgrade options tested at the limestone-reagent systems included the use of organic acid additives (dibasic acid (DBA) and/or sodium formate) as well as increased reagent ratio (higher excess limestone levels in the recirculating slurry solids) and absorber liquid-to-gas ratio. One system also tested operating at higher flue gas velocities to allow the existing FGD system to treat flue gas from an adjacent, unscrubbed unit. Upgrade options for the one lime-based system tested included increased absorber venturi pressure drop and increased sulfite concentration in the recirculating slurry liquor.

Gary M. Blythe; James L. Phillips

1997-10-15T23:59:59.000Z

373

Laboratory study for removal of organic sulfur from coal. Quarterly technical progress report  

SciTech Connect

Substantial progress has been made in the development of the Gravimelt Process for removal of organic sulfur from coal. Three reactors have been fabricated for both material balance studies of the desulfurization of coal with caustic and examination of the behavior of model organic and inorganic sulfur-containing compounds with the same mixture. Model organic sulfur conpounds have been procured and samples of Kentucky No. 9 coal enriched in mineral matter and samples enriched in organic matter have been prepared by float sink techniques for use in determining mechanism and products of the desulfurization reactions. Initial experimentation has been aimed at determining the fate of sulfur removed from coal and obtaining semi-quantitative information for future material balance studies. These studies show near 90% of the sulfur content of the Kentucky No. 9 coal was removed and approximately 3/4 of this removed sulfur was found by chemical analysis to be in the caustic phase. It was further determined that approximately 1% of the coal organic matter dissolves into the caustic phase. These results indicate rough material flows and show that material balance measurements are feasible. A preliminary conceptual engineering design for a full scale Gravimelt coal desulfurization plant was prepared in order to guide future laboratory efforts toward obtaining key engineering data. The engineering study indicates that the Gravimelt Process can be designed utilizing state of the art equipment and that likely energy recovery is approximately 90%. It is estimated that coal desulfurization costs will be in the range of $20 per ton of coal produced, or $.70/10/sup 6/ Btu, in 1980 dollars.

1980-07-01T23:59:59.000Z

374

Reducing acid leaching of manganiferous ore: Effect of the iron removal operation on solid waste disposal  

Science Conference Proceedings (OSTI)

The process of reducing acid leaching of manganiferous ore is aimed at the extraction of manganese from low grade manganese ores. This work is focused on the iron removal operation. The following items have been considered in order to investigate the effect of the main operating conditions on solid waste disposal and on the process costs: (i) type and quantity of the base agent used for iron precipitation, (ii) effective need of leaching waste separation prior to the iron removal operation, (iii) presence of a second leaching stage with the roasted ore, which might also act as a preliminary iron removal step, and (iv) effect of tailings washing on the solid waste classification. Different base compounds have been tested, including CaO, CaCO{sub 3}, NaOH, and Na{sub 2}CO{sub 3}. The latter gave the best results concerning both the precipitation process kinetics and the reagent consumption. The filtration of the liquor leach prior to iron removal was not necessary, implying significant savings in capital costs. A reduction of chemical consumption and an increase of manganese concentration in the solution were obtained by introducing secondary leaching tests with the previously roasted ore; this additional step was introduced without a significant decrease of global manganese extraction yield. Finally, toxicity characteristic leaching procedure (TCLP) tests carried out on the leaching solid waste showed: (i) a reduction of arsenic mobility in the presence of iron precipitates, and (ii) the need for a washing step in order to produce a waste that is classifiable as not dangerous, taking into consideration the existing Environmental National Laws.

De Michelis, Ida; Ferella, Francesco [University of L'Aquila, Department of Chemistry, Chemical Engineering and Materials, Monteluco di Roio, 67040 L'Aquila (Italy); Beolchini, Francesca [Polytechnic University of Marche, Department of Marine Sciences, Via Brecce Bianche, 60131 Ancona (Italy)], E-mail: f.beolchini@univpm.it; Veglio, Francesco [University of L'Aquila, Department of Chemistry, Chemical Engineering and Materials, Monteluco di Roio, 67040 L'Aquila (Italy)

2009-01-15T23:59:59.000Z

375

Removal of radioactive and other hazardous material from fluid waste  

DOE Patents (OSTI)

Hollow glass microspheres obtained from fly ash (cenospheres) are impregnated with extractants/ion-exchangers and used to remove hazardous material from fluid waste. In a preferred embodiment the microsphere material is loaded with ammonium molybdophosphonate (AMP) and used to remove radioactive ions, such as cesium-137, from acidic liquid wastes. In another preferred embodiment, the microsphere material is loaded with octyl(phenyl)-N-N-diisobutyl-carbamoylmethylphosphine oxide (CMPO) and used to remove americium and plutonium from acidic liquid wastes.

Tranter, Troy J. (Idaho Falls, ID); Knecht, Dieter A. (Idaho Falls, ID); Todd, Terry A. (Aberdeen, ID); Burchfield, Larry A. (W. Richland, WA); Anshits, Alexander G. (Krasnoyarsk, RU); Vereshchagina, Tatiana (Krasnoyarsk, RU); Tretyakov, Alexander A. (Zheleznogorsk, RU); Aloy, Albert S. (St. Petersburg, RU); Sapozhnikova, Natalia V. (St. Petersburg, RU)

2006-10-03T23:59:59.000Z

376

Thiacrown polymers for removal of mercury from waste streams  

DOE Patents (OSTI)

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

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

2002-01-01T23:59:59.000Z

377

Heat recirculating cooler for fluid stream pollutant removal  

DOE Patents (OSTI)

A process by which heat is removed from a reactant fluid to reach the operating temperature of a known pollutant removal method and said heat is recirculated to raise the temperature of the product fluid. The process can be utilized whenever an intermediate step reaction requires a lower reaction temperature than the prior and next steps. The benefits of a heat-recirculating cooler include the ability to use known pollutant removal methods and increased thermal efficiency of the system.

Richards, George A. (Morgantown, WV); Berry, David A. (Morgantown, WV)

2008-10-28T23:59:59.000Z

378

Aza crown ether compounds as anion receptors  

DOE Patents (OSTI)

A family of aza-ether based compounds including linear, multi-branched and aza-crown ethers is provided. When added to non-aqueous battery electrolytes, the new family of aza-ether based compounds acts as neutral receptors to complex the anion moiety of the electrolyte salt thereby increasing the conductivity and the transference number of LI{sup +} ion in alkali metal batteries. 3 figs.

Lee, H.S.; Yang, X.O.; McBreen, J.

1998-08-04T23:59:59.000Z

379

Aza crown ether compounds as anion receptors  

SciTech Connect

A family of aza-ether based compounds including linear, multi-branched and aza-crown ethers is provided. When added to non-aqueous battery electrolytes, the new family of aza-ether based compounds acts as neutral receptors to complex the anion moiety of the electrolyte salt thereby increasing the conductivity and the transference number of LI.sup.+ ion in alkali metal batteries.

Lee, Hung Sui (East Setauket, NY); Yang, Xiao-Oing (Port Jefferson Station, NY); McBreen, James (Bellport, NY)

1998-08-04T23:59:59.000Z

380

GTRI: Removing Vulnerable Civilian Nuclear and Radiological Material |  

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

Removing Vulnerable Civilian Nuclear and Radiological Material | Removing Vulnerable Civilian Nuclear and Radiological Material | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > Media Room > Fact Sheets > GTRI: Removing Vulnerable Civilian Nuclear and Radiological Material Fact Sheet GTRI: Removing Vulnerable Civilian Nuclear and Radiological Material

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


381

Application of Feed and Bleed Operations to Remove High Level ...  

Cleaning Method Phase Date. 5 Process Identification • After Mechanical Sludge Removal and Chemical Cleaning: ... Block Diagram Filtrate Solids Separation Solids Slurry

382

Organoclay Sorbent for Removal of Carbon Dioxide from Gas ...  

Organoclay Sorbent for Removal of Carbon Dioxide from Gas ... required for sequestration, an area of research identified as a high priority

383

Removal of Last Remaining HEU from Vietnam - Time Lapse Video...  

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

(MOST) and the Russian Federation successfully removed 11 kilograms of highly enriched uranium (HEU) from the Dalat Nuclear Research Institute. This is the eleventh country...

384

Heading Error Removal System for Tracking Devices - Energy ...  

Systems are able to reduce or remove slowly-varying drift errors, such as heading errors, rate of rotation errors, and direction of travel errors, to correct the ...

385

GTRI: Removing Vulnerable Civilian Nuclear and Radiological Material |  

National Nuclear Security Administration (NNSA)

Removing Vulnerable Civilian Nuclear and Radiological Material | Removing Vulnerable Civilian Nuclear and Radiological Material | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > Media Room > Fact Sheets > GTRI: Removing Vulnerable Civilian Nuclear and Radiological Material Fact Sheet GTRI: Removing Vulnerable Civilian Nuclear and Radiological Material

386

NETL: News Release - NETL Patented CO2-Removal Sorbents Promise...  

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

Power and Cost Savings DOE Laboratory Signs License Agreement Incorporating Sorbents in HVAC Add-on Technology Washington, DC - Carbon dioxide removal sorbents developed by the...

387

A New Method to Evaluate Hydrogen Sulfide Removal from Biogas.  

E-Print Network (OSTI)

??Hydrogen sulfide in biogas fuel increases the speed at which the system utilizing the biogas corrodes. This corrosion may be prevented by separating and removing… (more)

Martin, Jerry H II

2008-01-01T23:59:59.000Z

388

Impurity Removal from Petroleum Coke - Programmaster.org  

Science Conference Proceedings (OSTI)

Presentation Title, Impurity Removal from Petroleum Coke. Author(s), Alexandre Gagnon, Hans Darmstadt, Nigel Backhouse, Esme Ryan, Laurence Dyer, David ...

389

Comparative Analysis of Alternative Means for Removing Noncondensable...  

Open Energy Info (EERE)

study to compare six methods of removing noncondensable gases from direct-use geo-thermal steam power plants. This report defines the study methodologies and compares the...

390

Carbon ion pump for removal of carbon dioxide from combustion ...  

Biomass and Biofuels; Building Energy Efficiency; ... Carbon ion pump for removal of carbon dioxide from combustion gas and other gas mixtures United States Patent ...

391

Study of Alternative Approaches for Transite Panel Removal  

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

Bechtel Jacobs Company LLC (BJC) assembled an experienced team from both sites to evaluate both the manual and mechanical methods of transite panel removal.

392

Using Microwave Radiation for Removing Heavy Metal Ions and ...  

Science Conference Proceedings (OSTI)

Presentation Title, Using Microwave Radiation for Removing Heavy Metal Ions and Producing Biofuels. Author(s), Aharon Gedanken. On-Site Speaker (Planned ) ...

393

Sandia technology used to remove radioactive material at Fukushima...  

National Nuclear Security Administration (NNSA)

technology used to remove radioactive material at Fukushima | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the...

394

Hydrogen Removal From Heating Oil of a Parabolic Trough ...  

A Method to Selectively Remove & Measure Hydrogen Gas from a Fluid Volume Parabolic trough power plants use concentrated solar thermal energy to ...

395

Selective Removal of Thiophene from Liquid Fuels over Nickel ...  

Science Conference Proceedings (OSTI)

Presentation Title, Selective Removal of Thiophene from Liquid Fuels over Nickel -Based Nanocrystalline Zinc Oxide. Author(s), Mohammad Rafiqul Islam, Jewel ...

396

REMOVAL AND RECOVERY OF DEPOSITS FROM COAL GASIFICATION ...  

A method is provided for on-line removal and recovery of deposits from fossil fuel gasification systems to improve plant performance and recover a valuable metalloid.

397

Use, Maintenance, Removal, Inspections, and Safety of Dams (Iowa)  

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

This section describes operating plans for dams with movable structures, as well as procedures for raising or lowering of impoundment levels, dam removal, and dam safety inspections.

398

Method for Removal of Mercury from Various Gas Streams  

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

(NETL) is seeking licensing partners interested in implementing United States Patent Number 6,576,092 entitled "Method for Removal of Mercury from Various Gas Streams."...

399

Nitrogen removal from natural gas using two types of membranes ...  

A process for treating natural gas or other methane-rich gas to remove excess nitrogen. The invention relies on two-stage membrane separation, using ...

400

Process to remove rare earth from IFR electrolyte  

DOE Patents (OSTI)

The invention is a process for the removal of rare earths from molten chloride electrolyte salts used in the reprocessing of integrated fast reactor fuel (IFR). The process can be used either continuously during normal operation of the electrorefiner or as a batch process. The process consists of first separating the actinide values from the salt before purification by removal of the rare earths. After replacement of the actinides removed in the first step, the now-purified salt electrolyte has the same uranium and plutonium concentration and ratio as when the salt was removed from the electrorefiner.

Ackerman, John P. (Downers Grove, IL); Johnson, Terry R. (Wheaton, IL)

1994-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Process to remove rare earth from IFR electrolyte  

DOE Patents (OSTI)

The invention is a process for the removal of rare earths from molten chloride electrolyte salts used in the reprocessing of integrated fast reactor fuel (IFR). The process can be used either continuously during normal operation of the electrorefiner or as a batch process. The process consists of first separating the actinide values from the salt before purification by removal of the rare earths. After replacement of the actinides removed in the first step, the now-purified salt electrolyte has the same uranium and plutonium concentration and ratio as when the salt was removed from the electrorefiner. 1 fig.

Ackerman, J.P.; Johnson, T.R.

1994-08-09T23:59:59.000Z

402

Conventional methods for removing sulfur and other contaminants...  

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

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

403

Process to remove rare earth from IFR electrolyte  

DOE Patents (OSTI)

The invention is a process for the removal of rare earths from molten chloride electrolyte salts used in the reprocessing of integrated fast reactor fuel (IFR). The process can be used either continuously during normal operation of the electrorefiner or as a batch process. The process consists of first separating the actinide values from the salt before purification by removal of the rare earths. After replacement of the actinides removed in the first step, the now-purified salt electrolyte has the same uranium and plutonium concentration and ratio as when the salt was removed from the electrorefiner.

Ackerman, J.P.; Johnson, T.R.

1992-01-01T23:59:59.000Z

404

Mexico HEU Removal: Fact Sheet | National Nuclear Security Administrat...  

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

Mexico HEU Removal: Fact Sheet | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response...

405

Plutonium Removal from Sweden: Fact Sheet | National Nuclear...  

National Nuclear Security Administration (NNSA)

Removal from Sweden: Fact Sheet | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response...

406

US, International Partners Remove Last Remaining HEU from Vietnam...  

National Nuclear Security Administration (NNSA)

International Partners Remove Last Remaining HEU from Vietnam, Set Nuclear Security Milestone | National Nuclear Security Administration Our Mission Managing the Stockpile...

407

Retention of plutonium in mouse tissues as affected by antiviral compounds and their analogs  

SciTech Connect

The chelating agent DTPA (diethylenetriaminepentaacetic acid) is an effective therapeutic substance for decorporation of extracellar monomeric plutonium in the mouse and dog, but is much less effective in removing intracellular polymeric plutonium (Pu-P). In the absence of effective therapy, this intracellular plutonium is long retained in the body, particularly in reticuloendothelial tissues like the liver. Our interest, therefore, turned to the development of adjunct substances capable of removing additional plutonium from the liver beyond that removable by DTPA alone. We showed that glucan, a yeast cell wall polysaccharide, is a useful adjunct to DTPA for removal of Pu-P from the mouse liver. Its toxicity, however, makes it a less than desirable drug for potential human use. Therefore, we initiated a search for more soluble (and presumably less hazardous) therapeutic agents similar to glucan, i.e., capable of adjunct action with DTPA. Of over 20 substances tested the most successful results were obtained with two antiviral, antitumor compounds, the pyran copolymers XA-124-177 and XA-146-85-2. These are condensation products of divinyl ether and maleic anhydride. Another analog, EMH-227, prepared by condensation of acrylic acid and itaconic acid, was similarly successful. Maximal removal of plutonium from mouse liver was obtained with a single intravenous (I.V.) injection of 10 to 90 mg/kg of pyran copolymer given 5 days after I.V. Pu-P administration. Although these doses increased splenic uptake of plutonium, a dose of 10 mg/kg produced a minimal increase in the splenic burden while producing maximal removal of hepatic plutonium. (auth)

Lindenbaum, A.; Rosenthal, M.W.; Guilmette, R.A.

1975-01-01T23:59:59.000Z

408

EVALUATION OF ENHANCED VOC REMOVAL WITH SOIL FRACTURING IN THE SRS UPLAND UNIT  

Science Conference Proceedings (OSTI)

The Environmental Restoration Technology Section (ERTS) of the Savannah River National Laboratory (SRNL) conducted pilot scale testing to evaluate the effectiveness of using hydraulic fracturing as a means to improve soil vapor extraction (SVE) system performance. Laboratory and field research has shown that significant amounts of solvents can be entrapped in low permeability zones by capillary forces and removal by SVE can be severely limited due to low flow rates, mass transfer resistance of the hydrophobic compounds by trapped interparticle water, and diffusion resistance. Introducing sand-filled fractures into these tight zones improves the performance of SVE by (1) increasing the overall permeability of the formation and thereby increasing SVE flow rates, (2) shortening diffusion pathways, and (3) increasing air permeability by improving pore water removal. The synergistic effect of the fracture well completion methods, fracture and flow geometry, and pore water removal appears to increase the rate of solvent mass removal over that of increasing flow rate alone. A field test was conducted where a conventional well in the SRS Upland Unit was tested before and after hydraulic fracturing. ERTS teamed with Clemson University through the South Carolina University and Education Foundation (SCUREF) program utilizing their expertise in fracturing and fracture modeling. The goals of the fracturing pilot testing were to evaluate the following: (1) The effect of hydraulic fractures on the performance of a conventional well. This was the most reliable way to remove the effects of spatial variations in permeability and contaminant distribution on relative well performance. It also provided data on the option of improving the performance of existing wells using hydraulic fractures. (2) The relative performance of a conventional SVE well and isolated hydraulic fractures. This was the most reliable indicator of the performance of hydraulic fractures that could be created in a full-scale implementation. The SVE well, monitoring point arrays and four fracturing wells were installed and the well testing has been completed. Four fractures were successfully created the week of July 25, 2005. The fractures were created in an open area at the bottom of steel well casing by using a water jet to create a notch in the soil and then injecting a guar-sand slurry into the formation. The sand-filled fractures increase the effective air permeability of the subsurface formation diffusion path lengths for contaminant removal. The primary metrics for evaluation were an increase in SVE flow rates in the zone of contamination and an increase in the zone of influence. Sufficient testing has been performed to show that fracturing in the Upland Unit accelerates SVE solvent remediation and fracturing can increase flow rates in the Upland Unit by at least one order of magnitude.

Riha, B

2005-10-31T23:59:59.000Z

409

NDE Studies on CRDMs Removed From Service  

Science Conference Proceedings (OSTI)

Studies being conducted at the Pacific Northwest National Laboratory (PNNL) in Richland, Washington are focused on assessing the effectiveness of NDE inspections of control rod drive mechanism (CRDM) nozzles and J-groove weldments. The primary objective of this work is to provide information to the United States Nuclear Regulatory Commission (US NRC) on the effectiveness of ultrasonic testing (UT) and eddy current testing (ET) as related to the in-service inspection of CRDM nozzles and J-groove weldments, and to enhance the knowledge base of primary water stress corrosion cracking (PWSCC) through destructive characterization of the CRDM assemblies. In describing two CRDM assemblies removed from service, decontaminated, and then used in a series of NDE measurements, this paper will address the following questions: 1) What did each technique detect?, 2) What did each technique miss?, 3) How accurately did each technique characterize the detected flaws? Two CRDM assemblies including the CRDM nozzle, the J-groove weld, buttering, and a portion of the ferritic head material were selected for this study. One contained suspected PWSCC, based on in-service inspection data; the other contained evidence suggesting through-wall leakage, but this was unconfirmed. The selected NDE measurements follow standard industry techniques for conducting in-service inspections of CRDM nozzles and the crown of the J-groove welds and buttering. In addition, laboratory based NDE methods will be employed to conduct inspections of the CRDM assemblies, with particular emphasis on inspecting the J-groove weld and buttering. This paper will also describe the NDE methods used and discus the NDE results. Future work will involve using the results from these NDE studies to guide the development of a destructive characterization plan to reveal the crack morphology, to be compared with NDE responses.

Doctor, Steven R.; Cumblidge, Stephen E.; Schuster, George J.; Hockey, Ronald L.; Abrefah, John

2005-12-31T23:59:59.000Z

410

Measured performances of curved inverted-vee, absorber compound parabolic concentrating solar-energy collectors  

SciTech Connect

The design and thermal performance of modified compound parabolic concentrating (CPC) solar-energy collectors are described. The designs incorporate a curved inverted-Vee absorber fin, which allows a reflector of simple geometry to be used. This CPC collector, has exhibited a superior performance to that of a conventional cusp-reflector CPC design, owing to the enhancement of the optical efficiency obtained by eliminating gap optical losses and an enhanced heat removal factor. The consequence upon the performance of a further design refinement, which inhibited the convective heat losses, is also reported.

Norton, B. (Univ. of Ulster at Jordanstown (Ireland)); Prapas, D.E. (Aristotle Univ. of Thessaloniki (Greece)); Eames, P.C.; Probert, S.D. (Cranfield Institute of Technology, Bedford (England))

1989-01-01T23:59:59.000Z

411

Atmospheric Environment 41 (2007) 31513160 Ozone removal by HVAC filters  

E-Print Network (OSTI)

Atmospheric Environment 41 (2007) 3151­3160 Ozone removal by HVAC filters P. Zhao, J.A. Siegel�, R May 2006; accepted 14 June 2006 Abstract Residential and commercial HVAC filters that have been loaded of the relative importance of HVAC filters as a removal mechanism for ozone in residential and commercial

Siegel, Jeffrey

412

Process for selected gas oxide removal by radiofrequency catalysts  

DOE Patents (OSTI)

This process to remove gas oxides from flue gas utilizes adsorption on a char bed subsequently followed by radiofrequency catalysis enhancing such removal through selected reactions. Common gas oxides include SO[sub 2] and NO[sub x]. 1 figure.

Cha, C.Y.

1993-09-21T23:59:59.000Z

413

Process for removing pyritic sulfur from bituminous coals  

DOE Patents (OSTI)

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

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

1990-01-01T23:59:59.000Z

414

A Simple Rapid Method for the Removal of Leukocytes From  

E-Print Network (OSTI)

Filtration of human blood cells through lamb's wool columns removed more than 96 % of all leukocytes in a series of experiments, while the retention of erythrocytes by the column averaged 6.4%. This method should prove extremely useful for obtaining pure erythrocyte preparations for use in biochemical and physiological studies, and for removing leukocytes from blood prior to transfusion.

Human Blood; Edward Palmer; Frederic Waldman; William Dewitt

1973-01-01T23:59:59.000Z

415

Continuous cryopump with a method for removal of solidified gases  

DOE Patents (OSTI)

An improved cryopump for the removal of gases from a high vacuum, comprising a cryopanel incorporating honeycomb structure, refrigerant means thermally connected to the cryopanel, and a rotatable channel moving azimuthally around an axis located near the center of the cryopanel, removing gases adsorbed within the honeycomb structure by subliming them and conducting them outside the vacuum vessel. 4 figs.

Carlson, L.W.; Herman, H.

1988-05-05T23:59:59.000Z

416

Nuclear Maintenance Applications Center: Condenser Air Removal Equipment Maintenance Guide  

Science Conference Proceedings (OSTI)

The Condenser Air Removal Equipment Maintenance Guide provides power plant maintenance personnel with current maintenance information on this system. This guide will assist the plant maintenance personnel in improving reliability and reducing maintenance costs for the condenser air removal (CAR) equipment.

2007-12-21T23:59:59.000Z

417

A Method for Noise Removal of LIDAR Point Clouds  

Science Conference Proceedings (OSTI)

LiDAR can quickly and accurately obtain precision and high-density surface elevation data. In cooperation with high-precision GPS positioning technology and IMU attitude sensor, a typical noise removal algorithm of LIDAR point clouds based on FEA is ... Keywords: LIDAR, point clouds, noise removal, FEA

Huang Zuowei, Huang Yuanjiang, Huang Jie

2013-01-01T23:59:59.000Z

418

Polymers containing borane or carborane cage compounds and related applications  

DOE Patents (OSTI)

Polymers comprising residues of cage compound monomers having at least one polyalkoxy silyl substituent are provided. The cage compound monomers are selected from borane cage compound monomers comprising at least 7 cage atoms and/or carborane cage compound monomers comprising 7 to 11 cage compound monomers. Such polymers can further comprise one or more reactive matrices and/or co-monomers covalently bound with the cage compound monomer residues. Articles of manufacture comprising such polymers are also disclosed.

Bowen, III, Daniel E; Eastwood, Eric A

2013-04-23T23:59:59.000Z

419

Two stage sorption of sulfur compounds  

DOE Patents (OSTI)

A two stage method for reducing the sulfur content of exhaust gases is disclosed. Alkali- or alkaline-earth-based sorbent is totally or partially vaporized 10 and introduced into a sulfur-containing gas stream. The activated sorbent can be introduced in the reaction zone or the exhaust gases of a combustor or a gasifier. High efficiencies of sulfur removal can be achieved.

Moore, W.E.

1991-12-31T23:59:59.000Z

420

Two stage sorption of sulfur compounds  

DOE Patents (OSTI)

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

Moore, William E. (Manassas, VA)

1992-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Mexico HEU Removal: Fact Sheet | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Mexico HEU Removal: Fact Sheet | National Nuclear Security Administration Mexico HEU Removal: Fact Sheet | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > Media Room > Fact Sheets > Mexico HEU Removal: Fact Sheet Fact Sheet Mexico HEU Removal: Fact Sheet Mar 26, 2012 At the 2012 Nuclear Security Summit, the United States, Mexico and Canada announced the successful removal of HEU from Mexico and conversion of the

422

Savannah River Site Removes Dome, Opening Reactor for Recovery Act  

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

Savannah River Site Removes Dome, Opening Reactor for Recovery Act Savannah River Site Removes Dome, Opening Reactor for Recovery Act Decommissioning Savannah River Site Removes Dome, Opening Reactor for Recovery Act Decommissioning American Recovery and Reinvestment Act workers achieved a significant milestone in the decommissioning of a Cold War reactor at the Savannah River Site this month after they safely removed its rusty, orange, 75-foot-tall dome. With the help of a 660-ton crane and lifting lugs, the workers pulled the 174,000-pound dome off the Heavy Water Components Test Reactor, capping more than 16 months of preparations. Savannah River Site Removes Dome, Opening Reactor for Recovery Act Decommissioning More Documents & Publications Recovery Act Changes Hanford Skyline with Explosive Demolitions Recovery Act Workers Add Time Capsule Before Sealing Reactor for Hundreds

423

Composition And Method For Removing Photoresist Materials From Electronic  

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

Composition And Method For Removing Photoresist Materials From Composition And Method For Removing Photoresist Materials From Electronic Components Composition And Method For Removing Photoresist Materials From Electronic Components The invention is a combination of at least one dense phase fluid and at least one dense phase fluid modifier. Available for thumbnail of Feynman Center (505) 665-9090 Email Composition And Method For Removing Photoresist Materials From Electronic Components The invention is a combination of at least one dense phase fluid and at least one dense phase fluid modifier which can be used to contact substrates for electronic parts such as semiconductor wafers or chips to remove photoresist materials which are applied to the substrates during manufacture of the electronic parts. The dense phase fluid modifier is one

424

Compound and Elemental Analysis At Salt Wells Area (Shevenell...  

Open Energy Info (EERE)

Compound and Elemental Analysis At Salt Wells Area (Shevenell & Garside, 2003) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Compound and...

425

Alloys and Compounds for Thermoelectric and Solar Cell Applications  

Science Conference Proceedings (OSTI)

Alloys and Compounds for Thermoelectric and Solar Cell Applications II: Alloys and Compounds for Thermoelectric and Solar Cell Applications: Thermoelectric I

426

Energy-efficient indoor volatile organic compound air cleaning...  

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

Energy-efficient indoor volatile organic compound air cleaning using activated carbon fiber media with nightly regeneration Title Energy-efficient indoor volatile organic compound...

427

Compound and Elemental Analysis At Black Warrior Area (DOE GTP...  

Open Energy Info (EERE)

Compound and Elemental Analysis At Black Warrior Area (DOE GTP) Exploration Activity Details Location Black Warrior Area Exploration Technique Compound and Elemental Analysis...

428

Compound and Elemental Analysis At Wister Area (DOE GTP) | Open...  

Open Energy Info (EERE)

Compound and Elemental Analysis At Wister Area (DOE GTP) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Compound and Elemental Analysis At...

429

Conversion of depleted uranium hexafluoride to a solid uranium compound  

DOE Patents (OSTI)

A process for converting UF.sub.6 to a solid uranium compound such as UO.sub.2 and CaF. The UF.sub.6 vapor form is contacted with an aqueous solution of NH.sub.4 OH at a pH greater than 7 to precipitate at least some solid uranium values as a solid leaving an aqueous solution containing NH.sub.4 OH and NH.sub.4 F and remaining uranium values. The solid uranium values are separated from the aqueous solution of NH.sub.4 OH and NH.sub.4 F and remaining uranium values which is then diluted with additional water precipitating more uranium values as a solid leaving trace quantities of uranium in a dilute aqueous solution. The dilute aqueous solution is contacted with an ion-exchange resin to remove substantially all the uranium values from the dilute aqueous solution. The dilute solution being contacted with Ca(OH).sub.2 to precipitate CaF.sub.2 leaving dilute NH.sub.4 OH.

Rothman, Alan B. (Willowbrook, IL); Graczyk, Donald G. (Lemont, IL); Essling, Alice M. (Elmhurst, IL); Horwitz, E. Philip (Naperville, IL)

2001-01-01T23:59:59.000Z

430

SEPARATION PROCESS FOR ZIRCONIUM AND COMPOUNDS THEREOF  

DOE Patents (OSTI)

The separation of zirconium from columbium, rare earths, yttrium and the alkaline earth metals, such mixtures of elements occurring in zirconium ores or neutron irradiated uranium is described. According to the invention a suitable separation of zirconium from a one normal acidic aqueous solution containing salts, nitrates for example, of tetravalent zirconium, pentavalent columbium, yttrium, rare earths in the trivalent state and alkaline earths can be obtained by contacting the aqueous solution with a fluorinated beta diketonc alone or in an organic solvent solution, such as benzene, to form a zirconium chelate compound. When the organic solvent is present the zirconium chelate compound is directly extracted; otherwise it is separated by filtration. The zirconium may be recovered from contacting the organic solvent solution containing the chelated compound by back extraction with either an aqueous hydrofluoric acid or an oxalic acid solution.

Crandall, H.W.; Thomas, J.R.

1959-06-30T23:59:59.000Z

431

APPLICATIONS OF LAYERED DOUBLE HYDROXIDES IN REMOVING OXYANIONS FROM OIL REFINING AND COAL MINING WASTEWATER  

SciTech Connect

Western Research Institute (WRI), in conjunction with the U.S. Department of Energy (DOE), conducted a study of using the layered double hydroxides (LDH) as filter material to remove microorganisms, large biological molecules, certain anions and toxic oxyanions from various waste streams, including wastewater from refineries. Results demonstrate that LDH has a high adsorbing capability to those compounds with negative surface charge. Constituents studied include model bacteria, viruses, arsenic, selenium, vanadium, diesel range hydrocarbons, methyl tert-butyl ether (MTBE), mixed petroleum constituents, humic materials and anions. This project also attempted to modify the physical structure of LDH for the application as a filtration material. Flow characterizations of the modified LDH materials were also investigated. Results to date indicate that LDH is a cost-effective new material to be used for wastewater treatment, especially for the treatment of anions and oxyanions.

Song Jin; Paul Fallgren

2006-03-01T23:59:59.000Z

432

Inelastic neutron scattering in valence fluctuation compounds  

SciTech Connect

The valence fluctuation compounds are rare earth intermetallics where hybridization of the nearly-localized 4f electrons with the conduction electrons leads to incorporation of the 4f's into the itinerant states. This hybridization slows down the conduction electrons and hence gives them a heavy effective mass, justifying application of the term 'heavy Fermion' (HF) to these materials. During the project period, we grew large single crystals of several such compounds and measured their properties using both standard thermodynamic probes and state-of-the-art inelastic neutron scattering. We obtained three main results. For the intermediate valence compounds CePd{sub 3} and YbAl{sub 3}, we showed that the scattering of neutrons by the fluctuations of the 4f magnetic moment does not have the momentum dependence expected for the itinerant heavy mass state; rather, the scattering is more typical of a localized spin fluctuation. We believe that incoherent scattering localizes the excitation. For the heavy Fermion compound Ce(Ni{sub 0.935}Pd{sub 0.065}){sub 2}Ge{sub 2}, which sits at a T = 0 critical point for transformation into an antiferromagnetic (AF) phase, we showed that the scattering from the AF fluctuations does not exhibit any of the divergences that are expected at a phase transition. We speculate that alloy disorder profoundly suppresses the growth of the fluctuating AF regions, leading to short range clusters rather than regions of infinite size. Finally, we explored the applicability of key concepts used to describe the behavior of rare earth heavy Fermions to uranium based HF compounds where the 5f electrons are itinerant as opposed to localized. We found that scaling laws relating the spin fluctuation energy measured in neutron scattering to the low temperature specific heat and susceptibility are valid for the uranium compounds, once corrections are made for AF fluctuations; however, the degeneracy of the high temperature moment is smaller than expected for rare-earth-like Hund's rule behavior, essentially because the orbital moment is suppressed for itinerant 5f electrons. We also found that the standard local-moment-based theory of the temperature dependence of the specific heat, susceptibility and neutron scattering fails badly for URu{sub 2}Zn{sub 20} and UCo{sub 2}Zn{sub 20}, even though the theory is phenomenally successful for the closely related rare earth compound YbFe{sub 2}Zn{sub 20}. Both these results highlight the distinction between the itineracy of the 5f's and the localization of the 4f's. It is our hope that these results are sufficiently significant as to stimulate deeper investigation of these compounds.

Jon M Lawrence

2011-02-15T23:59:59.000Z

433

Process for producing phenolic compounds from lignins  

DOE Patents (OSTI)

A process is described for the production of low molecular weight phenolic compounds from lignins through the pyrolysis of the lignins in the presence of a strong base. In a preferred embodiment, potassium hydroxide is present in an amount of from about 0.1% to about 5% by weight, the pyrolysis temperature is from about 400 C to about 600 C at atmospheric pressure, and the time period for substantial completion of the reaction is from about 1--3 minutes. Examples of low molecular weight phenolic compounds produced include methoxyphenols, non-methoxylated phenols, and mixtures thereof. 16 figs.

Agblevor, F.A.

1998-09-15T23:59:59.000Z

434

Organic photosensitive devices using subphthalocyanine compounds  

DOE Patents (OSTI)

An organic photosensitive optoelectronic device, having a donor-acceptor heterojunction of a donor-like material and an acceptor-like material and methods of making such devices is provided. At least one of the donor-like material and the acceptor-like material includes a subphthalocyanine, a subporphyrin, and/or a subporphyrazine compound; and/or the device optionally has at least one of a blocking layer or a charge transport layer, where the blocking layer and/or the charge transport layer includes a subphthalocyanine, a subporphyrin, and/or a subporphyrazine compound.

Rand, Barry (Princeton, NJ); Forrest, Stephen R. (Ann Arbor, MI); Mutolo, Kristin L. (Hollywood, CA); Mayo, Elizabeth (Alhambra, CA); Thompson, Mark E. (Anaheim Hills, CA)

2011-07-05T23:59:59.000Z

435

Process for producing phenolic compounds from lignins  

DOE Patents (OSTI)

A process for the production of low molecular weight phenolic compounds from lignins through the pyrolysis of the lignins in the presence of a strong base. In a preferred embodiment, potassium hydroxide is present in an amount of from about 0.1% to about 5% by weight, the pyrolysis temperature is from about 400.degree. C. to about 600.degree. C. at atmospheric pressure, and the time period for substantial completion of the reaction is from about 1-3 minutes. Examples of low molecular weight phenolic compounds produced include methoxyphenols, non-methoxylated phenols, and mixtures thereof.

Agblevor, Foster A. (Lakewood, CO)

1998-01-01T23:59:59.000Z

436

Micro-aeration for hydrogen sulfide removal from biogas.  

E-Print Network (OSTI)

??The presence of sulfur compounds (e.g. protein, sulfate, thiosulfate, sulfite, etc.) in the feed stream generates highly corrosive and odorous hydrogen sulfide during anaerobic digestion.… (more)

Duangmanee, Thanapong

2009-01-01T23:59:59.000Z

437

High Energy Laser for Space Debris Removal  

SciTech Connect

The National Ignition Facility (NIF) and Photon Science Directorate at Lawrence Livermore National Laboratory (LLNL) has substantial relevant experience in the construction of high energy lasers, and more recently in the development of advanced high average power solid state lasers. We are currently developing new concepts for advanced solid state laser drivers for the Laser Inertial Fusion Energy (LIFE) application, and other high average power laser applications that could become central technologies for use in space debris removal. The debris population most readily addressed by our laser technology is that of 0.1-10 cm sized debris in low earth orbit (LEO). In this application, a ground based laser system would engage an orbiting target and slow it down by ablating material from its surface which leads to reentry into the atmosphere, as proposed by NASA's ORION Project. The ORION concept of operations (CONOPS) is also described in general terms by Phipps. Key aspects of this approach include the need for high irradiance on target, 10{sup 8} to 10{sup 9} W/cm{sup 2}, which favors short (i.e., picoseconds to nanoseconds) laser pulse durations and high energy per pulse ({approx} > 10 kJ). Due to the target's orbital velocity, the potential duration of engagement is only of order 100 seconds, so a high pulse repetition rate is also essential. The laser technology needed for this application did not exist when ORION was first proposed, but today, a unique combination of emerging technologies could create a path to enable deployment in the near future. Our concepts for the laser system architecture are an extension of what was developed for the National Ignition Facility (NIF), combined with high repetition rate laser technology developed for Inertial Fusion Energy (IFE), and heat capacity laser technology developed for military applications. The 'front-end' seed pulse generator would be fiber-optics based, and would generate a temporally, and spectrally tailored pulse designed for high transmission through the atmosphere, as well as efficient ablative coupling to the target. The main amplifier would use either diode-pumped or flashlamp-pumped solid state gain media, depending on budget constraints of the project. A continuously operating system would use the gas-cooled amplifier technology developed for Mercury, while a burst-mode option would use the heat capacity laser technology. The ground-based system that we propose is capable of rapid engagement of targets whose orbits cross over the site, with potential for kill on a single pass. Very little target mass is ablated per pulse so the potential to create additional hazardous orbiting debris is minimal. Our cost estimates range from $2500 to $5000 per J depending on choices for laser gain medium, amplifier pump source, and thermal management method. A flashlamp-pumped, Nd:glass heat-capacity laser operating in the burst mode would have costs at the lower end of this spectrum and would suffice to demonstrate the efficacy of this approach as a prototype system. A diode-pumped, gas-cooled laser would have higher costs but could be operated continuously, and might be desirable for more demanding mission needs. Maneuverability can be incorporated in the system design if the additional cost is deemed acceptable. The laser system would need to be coupled with a target pointing and tracking telescope with guide-star-like wavefront correction capability.

Barty, C; Caird, J; Erlandson, A; Beach, R; Rubenchik, A

2009-10-30T23:59:59.000Z

438

High Energy Laser for Space Debris Removal  

SciTech Connect

The National Ignition Facility (NIF) and Photon Science Directorate at Lawrence Livermore National Laboratory (LLNL) has substantial relevant experience in the construction of high energy lasers, and more recently in the development of advanced high average power solid state lasers. We are currently developing new concepts for advanced solid state laser drivers for the Laser Inertial Fusion Energy (LIFE) application, and other high average power laser applications that could become central technologies for use in space debris removal. The debris population most readily addressed by our laser technology is that of 0.1-10 cm sized debris in low earth orbit (LEO). In this application, a ground based laser system would engage an orbiting target and slow it down by ablating material from its surface which leads to reentry into the atmosphere, as proposed by NASA's ORION Project. The ORION concept of operations (CONOPS) is also described in general terms by Phipps. Key aspects of this approach include the need for high irradiance on target, 10{sup 8} to 10{sup 9} W/cm{sup 2}, which favors short (i.e., picoseconds to nanoseconds) laser pulse durations and high energy per pulse ({approx} > 10 kJ). Due to the target's orbital velocity, the potential duration of engagement is only of order 100 seconds, so a high pulse repetition rate is also essential. The laser technology needed for this application did not exist when ORION was first proposed, but today, a unique combination of emerging technologies could create a path to enable deployment in the near future. Our concepts for the laser system architecture are an extension of what was developed for the National Ignition Facility (NIF), combined with high repetition rate laser technology developed for Inertial Fusion Energy (IFE), and heat capacity laser technology developed for military applications. The 'front-end' seed pulse generator would be fiber-optics based, and would generate a temporally, and spectrally tailored pulse designed for high transmission through the atmosphere, as well as efficient ablative coupling to the target. The main amplifier would use either diode-pumped or flashlamp-pumped solid state gain media, depending on budget constraints of the project. A continuously operating system would use the gas-cooled amplifier technology developed for Mercury, while a burst-mode option would use the heat capacity laser technology. The ground-based system that we propose is capable of rapid engagement of targets whose orbits cross over the site, with potential for kill on a single pass. Very little target mass is ablated per pulse so the potential to create additional hazardous orbiting debris is minimal. Our cost estimates range from $2500 to $5000 per J depending on choices for laser gain medium, amplifier pump source, and thermal management method. A flashlamp-pumped, Nd:glass heat-capacity laser operating in the burst mode would have costs at the lower end of this spectrum and would suffice to demonstrate the efficacy of this approach as a prototype system. A diode-pumped, gas-cooled laser would have higher costs but could be operated continuously, and might be desirable for more demanding mission needs. Maneuverability can be incorporated in the system design if the additional cost is deemed acceptable. The laser system would need to be coupled with a target pointing and tracking telescope with guide-star-like wavefront correction capability.

Barty, C; Caird, J; Erlandson, A; Beach, R; Rubenchik, A

2009-10-30T23:59:59.000Z

439

Fluorescent compounds for plastic scintillation applications  

SciTech Connect

Several 2-(2{prime}-hydroxyphenyl)benzothiazole, -benzoxazole, and -benzimidazole derivatives have been prepared. Transmittance, fluorescence, light yield, and decay time characteristics of these compounds have been studied in a polystyrene matrix and evaluated for use in plastic scintillation detectors. Radiation damage studies utilizing a {sup 60}C source have also been performed.

Pla-Dalmau, A.; Bross, A.D.

1994-04-01T23:59:59.000Z

440

Pyrolysis mechanisms of lignin model compounds  

DOE Green Energy (OSTI)

The flash vacuum pyrolysis of lignin model compounds was studied under conditions optimized for the production of liquid products to provide mechanistic insight into the reaction pathways that lead to product formation. The major reaction products can be explained by cleavage of the C-O either linkage by a free radial or concerted 1,2-elimination.

Britt, P.F.; Buchanan, A.C. III; Cooney, M.J.

1997-06-01T23:59:59.000Z

Note: This page contains sample records for the topic "removing asphalt compounds" 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

Compound nucleus studies withy reverse kinematics  

SciTech Connect

Reverse kinematics reactions are used to demonstrate the compound nucleus origin of intermediate mass particles at low energies and the extension of the same mechanism at higher energies. No evidence has appeared in our energy range for liquid-vapor equilibrium or cold fragmentation mechanisms. 11 refs., 12 figs.

Moretto, L.G.

1985-06-01T23:59:59.000Z

442

PRODUCTION OF URANIUM AND THORIUM COMPOUNDS  

DOE Patents (OSTI)

Compounds of Th and U are extracted with an organic solvent in the presence of an adsorbent substance which has greater retentivity for impurities present than for the uranium and/or thorium. The preferred adsorbent material is noted as being cellulose. The uranium and thoriumcontaining substances treated are preferably in the form of dissolved nitrates, and the preferred organic solvent is diethyl ether.

Arden, T.V.; Burstall, F.H.; Linstead, R.P.; Wells, R.A.

1955-12-27T23:59:59.000Z

443

Mercury removal at Idaho National Engineering and Environmental Laboratory's New Waste Calcining Facility  

SciTech Connect

Technologies were investigated to determine viable processes for removing mercury from the calciner (NWCF) offgas system at the Idaho National Engineering and Environmental Laboratory. Technologies for gas phase and aqueous phase treatment were evaluated. The technologies determined are intended to meet EPA Maximum Achievable Control Technology (MACT) requirements under the Clean Air Act and Resource Conservation and Recovery Act (RCRA). Currently, mercury accumulation in the calciner off-gas scrubbing system is transferred to the tank farm. These transfers lead to accumulation in the liquid heels of the tanks. The principal objective for aqueous phase mercury removal is heel mercury reduction. The system presents a challenge to traditional methods because of the presence of nitrogen oxides in the gas phase and high nitric acid in the aqueous scrubbing solution. Many old and new technologies were evaluated including sorbents and absorption in the gas phase and ion exchange, membranes/sorption, galvanic methods, and UV reduction in the aqueous phase. Process modifications and feed pre-treatment were also evaluated. Various properties of mercury and its compounds were summarized and speciation was predicted based on thermodynamics. Three systems (process modification, NOxidizer combustor, and electrochemical aqueous phase treatment) and additional technology testing were recommended.

S. C. Ashworth

2000-02-27T23:59:59.000Z

444

Mercury Removal at Idaho National Engineering and Environmental Laboratory's New Waste Calcining Facility  

SciTech Connect

Technologies were investigated to determine viable processes for removing mercury from the calciner (NWCF) offgas system at the Idaho National Engineering and Environmental Laboratory. Technologies for gas phase and aqueous phase treatment were evaluated. The technologies determined are intended to meet EPA Maximum Achievable Control Technology (MACT) requirements under the Clean Air Act and Resource Conservation and Recovery Act (RCRA). Currently, mercury accumulation in the calciner off-gas scrubbing system is transferred to the tank farm. These transfers lead to accumulation in the liquid heels of the tanks. The principal objective for aqueous phase mercury removal is heel mercury reduction. The system presents a challenge to traditional methods because of the presence of nitrogen oxides in the gas phase and high nitric acid in the aqueous scrubbing solution. Many old and new technologies were evaluated including sorbents and absorption in the gas phase and ion exchange, membranes/sorption, galvanic methods, and UV reduction in the aqueous phase. Process modifications and feed pre-treatment were also evaluated. Various properties of mercury and its compounds were summarized and speciation was predicted based on thermodynamics. Three systems (process modification, NOxidizer combustor, and electrochemical aqueous phase treatment) and additional technology testing were recommended.

Ashworth, Samuel Clay; Wood, R. A.; Taylor, D. D.; Sieme, D. D.

2000-03-01T23:59:59.000Z

445

Mechanistic study of chlorine removal from coal by high-temperature leaching  

SciTech Connect

The objectives of this research were to: (1) continue the experimental investigation of removal of chlorine from coal using high-temperature leaching techniques, (2) understand the mechanisms involved in the leaching of chlorine from coal, and (3) develop a mathematical model which can be used to correlate the data and to describe the performance of the process. Efforts involved developing procedures for estimation of effective pore volumes of coal samples and measurement of surface areas of coal samples by use of carbon dioxide rather than nitrogen. Different mesh sizes of Illinois No. 6 seam and Illinois No. 5 seam coals were evaluated. Based on the pore volume and CO{sub 2} surface areas obtained, average pore diameters were calculated for the samples examined. This information was compared to the chlorine removal of the coal samples that occurred during hot water leaching. A second aspect of this research involved study of chloride evolution rates from coal and model chlorine compounds heated in a tube furnace under continuous nitrogen flow. Kinetic parameters were determined. 3 refs., 6 figs., 3 tabs.

Chen, Han Lin (Southern Illinois Univ., Carbondale, IL (USA). Dept. of Technology); Muchmore, C.B. (Southern Illinois Univ., Carbondale, IL (USA). Dept. of Mechanical Engineering and Energy Processes)

1990-11-01T23:59:59.000Z

446

Adsorptive Membranes vs. Resins for Acetic Acid Removal from Biomass Hydrolysates  

Science Conference Proceedings (OSTI)

Acetic acid is a compound commonly found in hemicellulosic hydrolysates. This weak acid strongly influences the bioconversion of sugar containing hydrolysates. Previous investigators have used anion exchange resins for acetic acid removal from different hemicellulosic hydrolysates. In this study, the efficiency of an anion exchange membrane was compared to that of an anion exchange resin, for acetic acid removal from a DI water solution and an acidic hemicellulose hydrolysate pretreated using two different methods. Ion exchange membranes and resins have very different geometries. Here the performance of membranes and resins is compared using two dimensionless parameters, the relative mass throughput and chromatographic bed number. The relative mass throughput arises naturally from the Thomas solution for ion exchange. The results show that the membrane exhibit better performance in terms of capacity, and loss of the desired sugars. In addition acetic acid may be eluted at a higher concentration from the membrane thus leading to the possibility of recovery and re-use of the acetic acid.

Han, B.; Carvalho, W.; Canilha, L.; da Silva, S. S.; e Silva, J. B. A.; McMillan, J. D.; Wickramasinghe, S. R.

2006-01-01T23:59:59.000Z

447

Method of removing nitrogen monoxide from a nitrogen monoxide-containing gas using a water-soluble iron ion-dithiocarbamate, xanthate or thioxanthate  

DOE Patents (OSTI)

The present invention relates to a method of removing of nitrogen monoxide from a nitrogen monoxide-containing gas which method comprises contacting a nitrogen oxide-containing gas with an aqueous solution of water soluble organic compound-iron ion chelate complex. The NO absorption efficiency of ferrous urea-dithiocarbamate and ferrous diethanolamine-xanthate as a function of time, oxygen content and solution ph is presented. 3 figs., 1 tab.

Liu, D. Kwok-Keung; Chang, Shih-Ger

1987-08-25T23:59:59.000Z

448

In situ removal of the ``hockey stick`` fissile material deposit at the East Tennessee Technology Park  

Science Conference Proceedings (OSTI)

Prior to shutdown of the gaseous diffusion process at the Oak Ridge K-25 Plant (now East Tennessee Technology Park), leakage of humid air into the process piping and equipment caused reactions with UF{sub 6}, which produced nonvolatile uranyl fluoride (UO{sub 2}F{sub 2}) deposition and other solid uranium fluoride compounds. During the period 1988--1991, Lockheed Martin Energy Systems performed nondestructive analysis (NDA) radiological surveys of the K-25 Site process facilities that previously had contained or processed uranium. These surveys were made to estimate the mass and {sup 235}U assay of localized uranium deposits remaining within the process piping and equipment. Three deposits were identified that had sufficient mass to achieve criticality. Two of these, the horizontal pipe and the T pipe deposits, required the addition of a moderator before a criticality accident could occur. The third was a very large uranium deposit determined by NDA to be distributed annularly in the process piping. Because of the shape of the system, it came to be called the hockey stick deposit. Because of the foregoing concerns with the hockey stick deposit, it was decided to gain experience by removing the less hazardous smaller deposits with their less complicated geometries first. Thus, the horizontal pipe deposit, the simplest and least reactive case, was handled first, in June 1997. Next, the T pipe, which was an intersection of large-diameter pipes and which posed additional problems because of a more complex geometry, was handled in August 1997. From this experience, the deposit removal techniques and procedures were refined. In December 1997, this large deposit was removed, and the contents were placed in a safe array configuration.

Lewis, K.D.; Tollefson, D.A. [Lockheed Martin Energy Systems (United States)

1998-12-31T23:59:59.000Z

449

Tritium labeling of organic compounds deposited on porous structures  

DOE Patents (OSTI)

An improved process for labeling organic compounds with tritium is carried out by depositing the selected compound on the extensive surface of a porous structure such as a membrane filter and exposing the membrane containing the compound to tritium gas activated by the microwave discharge technique. The labeled compound is then recovered from the porous structure.

Ehrenkaufer, Richard L. E. (Speonk, NY); Wolf, Alfred P. (Setauket, NY); Hembree, Wylie C. (Woodcliff Lake, NJ)

1979-01-01T23:59:59.000Z

450

Compositions containing borane or carborane cage compounds and related applications  

DOE Patents (OSTI)

Compositions comprising a polymer-containing matrix and a filler comprising a cage compound selected from borane cage compounds, carborane cage compounds, metal complexes thereof, residues thereof, mixtures thereof, and/or agglomerations thereof, where the cage compound is not covalently bound to the matrix polymer. Methods of making and applications for using such compositions are also disclosed.

Bowen, III, Daniel E; Eastwood, Eric A

2013-05-28T23:59:59.000Z

451

Plutonium Removal from Sweden: Fact Sheet | National Nuclear Security  

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

Removal from Sweden: Fact Sheet | National Nuclear Security Removal from Sweden: Fact Sheet | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > Media Room > Fact Sheets > Plutonium Removal from Sweden: Fact Sheet Fact Sheet Plutonium Removal from Sweden: Fact Sheet Mar 27, 2012 Sweden has been a global leader on nonproliferation, and was one of the

452

Building Removal Ongoing at DOE's Paducah Site | Department of Energy  

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

Building Removal Ongoing at DOE's Paducah Site Building Removal Ongoing at DOE's Paducah Site Building Removal Ongoing at DOE's Paducah Site August 23, 2012 - 12:00pm Addthis Media Contact Buz Smith Robert.Smith@lex.doe.gov 270-441-6821 PADUCAH, KY - Work is ongoing at the Paducah Gaseous Diffusion Plant (PGDP) to raze a 65,000-square-foot facility known as the C-340 Metals Plant, which was used to make uranium metal during the Cold War. Department of Energy (DOE) cleanup contractor LATA Environmental Services of Kentucky began removing more than 1,500 panels of cement-asbestos siding from the Metals Plant complex Wednesday in anticipation of New Jersey-based LVI Services starting demolition Sept. 19. Demolition work is projected to last through the end of calendar 2012. "This is an important milestone because the C-340 Metals Plant is the

453

Czech Republic HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Czech Republic HEU Removal | National Nuclear Security Administration Czech Republic HEU Removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > Czech Republic HEU Removal Czech Republic HEU Removal Location Czech Republic United States 49° 35' 23.3628" N, 15° 4' 23.6712" E See map: Google Maps Printer-friendly version Printer-friendly version

454

High-Activity Radioactive Materials Removed From Mexico | National Nuclear  

National Nuclear Security Administration (NNSA)

High-Activity Radioactive Materials Removed From Mexico | National Nuclear High-Activity Radioactive Materials Removed From Mexico | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > Media Room > Press Releases > High-Activity Radioactive Materials Removed From Mexico Press Release High-Activity Radioactive Materials Removed From Mexico Nov 15, 2013 WASHINGTON, D.C. - The National Nuclear Security Administration (NNSA)

455

South Africa HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

South Africa HEU Removal | National Nuclear Security Administration South Africa HEU Removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > South Africa HEU Removal South Africa HEU Removal Location South Africa United States 30° 33' 35.0604" S, 22° 19' 27.1884" E See map: Google Maps Printer-friendly version Printer-friendly version

456

Ukraine Fuel Removal: Fact Sheet | National Nuclear Security Administration  

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

Ukraine Fuel Removal: Fact Sheet | National Nuclear Security Administration Ukraine Fuel Removal: Fact Sheet | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > Media Room > Fact Sheets > Ukraine Fuel Removal: Fact Sheet Fact Sheet Ukraine Fuel Removal: Fact Sheet Mar 26, 2012 For nearly two decades, the United States and Ukraine have cooperated on a

457

Moab Project Continues Progress on Tailings Removal with Contract  

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

Moab Project Continues Progress on Tailings Removal with Contract Moab Project Continues Progress on Tailings Removal with Contract Transition Moab Project Continues Progress on Tailings Removal with Contract Transition December 27, 2012 - 12:00pm Addthis Laborers place a disposable liner in a tailings container. Laborers place a disposable liner in a tailings container. MOAB, Utah - The Moab mill tailings removal project in Utah ended the year having shipped more than 35 percent of the total 16 million tons of uranium mill tailings off-site. The tailings are being transported by rail 30 miles north to a disposal cell for permanent storage. More than 1 million tons of tailings were shipped during fiscal year 2012, which closed at the end of September. The Moab Project also successfully transitioned both of its prime contracts

458

Sandia technology used to remove radioactive material at Fukushima |  

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

technology used to remove radioactive material at Fukushima | technology used to remove radioactive material at Fukushima | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > NNSA Blog > Sandia technology used to remove radioactive material ... Sandia technology used to remove radioactive material at Fukushima Posted By Office of Public Affairs

459

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

460

Moab Project Continues Progress on Tailings Removal with Contract  

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

Moab Project Continues Progress on Tailings Removal with Contract Moab Project Continues Progress on Tailings Removal with Contract Transition Moab Project Continues Progress on Tailings Removal with Contract Transition December 27, 2012 - 12:00pm Addthis Laborers place a disposable liner in a tailings container. Laborers place a disposable liner in a tailings container. MOAB, Utah - The Moab mill tailings removal project in Utah ended the year having shipped more than 35 percent of the total 16 million tons of uranium mill tailings off-site. The tailings are being transported by rail 30 miles north to a disposal cell for permanent storage. More than 1 million tons of tailings were shipped during fiscal year 2012, which closed at the end of September. The Moab Project also successfully transitioned both of its prime contracts

Note: This page contains sample records for the topic "removing asphalt compounds" 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.