National Library of Energy BETA

Sample records for uranyl nitrate solution

  1. Analysis of Enriched Uranyl Nitrate in Nested Annular Tank Array

    SciTech Connect (OSTI)

    John D. Bess; James D. Cleaver

    2009-06-01

    Two series of experiments were performed at the Rocky Flats Critical Mass Laboratory during the 1980s using highly enriched (93%) uranyl nitrate solution in annular tanks. [1, 2] Tanks were of typical sizes found in nuclear production plants. Experiments looked at tanks of varying radii in a co-located set of nested tanks, a 1 by 2 array, and a 1 by 3 array. The co-located set of tanks had been analyzed previously [3] as a benchmark for inclusion within the International Handbook of Evaluated Criticality Safety Benchmark Experiments. [4] The current study represents the benchmark analysis of the 1 by 3 array of a series of nested annular tanks. Of the seventeen configurations performed in this set of experiments, twelve were evaluated and nine were judged as acceptable benchmarks.

  2. FY-15 Progress Report on Cleanup of irradiated SHINE Target Solutions Containing 140g-U/L Uranyl Sulfate

    SciTech Connect (OSTI)

    Bennett, Megan E.; Bowers, Delbert L.; Vandegrift, George F.

    2015-09-01

    During FY 2012 and 2013, a process was developed to convert the SHINE Target Solution (STS) of irradiated uranyl sulfate (140 g U/L) to uranyl nitrate [1, 2]. This process is necessary so that the uranium solution can be processed by the UREX (Uranium Extraction) separation process, which will remove impurities from the uranium so that it can be recycled. The uranyl sulfate solution must contain <0.02 M SO42- so that the uranium will be extractable into the UREXsolvent [2]. In addition, it is desired that the barium content be below 0.0007 M, as this is the limit in the Resource Conservation and Recovery Act (RCRA).

  3. Uranyl nitrate-exposed rat alveolar macrophages cell death: Influence of superoxide anion and TNF ? mediators

    SciTech Connect (OSTI)

    Orona, N.S.; Tasat, D.R.

    2012-06-15

    Uranium compounds are widely used in the nuclear fuel cycle, military and many other diverse industrial processes. Health risks associated with uranium exposure include nephrotoxicity, cancer, respiratory, and immune disorders. Macrophages present in body tissues are the main cell type involved in the internalization of uranium particles. To better understand the pathological effects associated with depleted uranium (DU) inhalation, we examined the metabolic activity, phagocytosis, genotoxicity and inflammation on DU-exposed rat alveolar macrophages (12.5200 ?M). Stability and dissolution of DU could differ depending on the dissolvent and in turn alter its biological action. We dissolved DU in sodium bicarbonate (NaHCO{sub 3} 100 mM) and in what we consider a more physiological vehicle resembling human internal media: sodium chloride (NaCl 0.9%). We demonstrate that uranyl nitrate in NaCl solubilizes, enters the cell, and elicits its cytotoxic effect similarly to when it is diluted in NaHCO{sub 3}. We show that irrespective of the dissolvent employed, uranyl nitrate impairs cell metabolism, and at low doses induces both phagocytosis and generation of superoxide anion (O{sub 2}{sup ?}). At high doses it provokes the secretion of TNF? and through all the range of doses tested, apoptosis. We herein suggest that at DU low doses O{sub 2}{sup ?} may act as the principal mediator of DNA damage while at higher doses the signaling pathway mediated by O{sub 2}{sup ?} may be blocked, prevailing damage to DNA by the TNF? route. The study of macrophage functions after uranyl nitrate treatment could provide insights into the pathophysiology of uranium?related diseases. -- Highlights: ? Uranyl nitrate effect on cultured macrophages is linked to the doses and independent of its solubility. ? At low doses uranyl nitrate induces generation of superoxide anion. ? At high doses uranyl nitrate provokes secretion of TNF?. ? Uranyl nitrate induces apoptosis through all the range of doses tested.

  4. Highly Enriched Uranyl Nitrate in Annular Tanks with Concrete Reflection: 1 x 3 Line Array of Nested Pairs of Tanks

    SciTech Connect (OSTI)

    James Cleaver; John D. Bess; Nathan Devine; Fitz Trumble

    2009-09-01

    A series of seven experiments were performed at the Rocky Flats Critical Mass Laboratory beginning in August, 1980 (References 1 and 2). Highly enriched uranyl nitrate solution was introduced into a 1-3 linear array of nested stainless steel annular tanks. The tanks were inside a concrete enclosure, with various moderator and absorber materials placed inside and/or between the tanks. These moderators and absorbers included boron-free concrete, borated concrete, borated plaster, and cadmium. Two configurations included placing bottles of highly enriched uranyl nitrate between tanks externally. Another experiment involved nested hemispheres of highly enriched uranium placed between tanks externally. These three configurations are not evaluated in this report. The experiments evaluated here are part of a series of experiments, one set of which is evaluated in HEU-SOL-THERM-033. The experiments in this and HEU-SOL-THERM-033 were performed similarly. They took place in the same room and used the same tanks, some of the same moderators and absorbers, some of the same reflector panels, and uranyl nitrate solution from the same location. There are probably additional similarities that existed that are not identified here. Thus, many of the descriptions in this report are either the same or similar to those in the HEU-SOL-THERM-033 report. Seventeen configurations (sixteen of which were critical) were performed during seven experiments; six of those experiments are evaluated here with thirteen configurations. Two configurations were identical, except for solution height, and were conducted to test repeatability. The solution heights were averaged and the two were evaluated as one configuration, which gives a total of twelve evaluated configurations. One of the seventeen configurations was subcritical. Of the twelve critical configurations evaluated, nine were judged as acceptable as benchmarks.

  5. Uranyl-Peroxide Nanocapsules in Aqueous Solution: Force Field Development

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

    and First Applications | Center for Gas SeparationsRelevant to Clean Energy Technologies | Blandine Jerome Uranyl-Peroxide Nanocapsules in Aqueous Solution: Force Field Development and First Applications Previous Next List Pere Miró, Bess Vlaisavljevich, Allison L. Dzubak, Shuxian Hu, Peter C. Burns, Christopher J. Cramer, Riccardo Spezia, and Laura Gagliardi, J. Phys. Chem. C, 118, 24730-24740 (2014) DOI: 10.1021/jp504147s jp-2014-04147s_0009 Abstract: The self-assembly of uranyl-peroxide

  6. Structure and dynamics of aqueous solution of uranyl ions

    SciTech Connect (OSTI)

    Chopra, Manish; Choudhury, Niharendu

    2014-04-24

    The present work describes a molecular dynamics simulation study of structure and dynamics of aqueous solution of uranyl ions in water. Structural properties of the system in terms of radial distribution functions and dynamical characteristics as obtained through velocity autocorrelation function and mean square displacements have been analyzed. The results for radial distribution functions show the oxygen of water to form the first solvation shell at 2.4 around the uranium atom, whereas the hydrogen atoms of water are distributed around the uranium atom with the major peak at around 3.0 . Analyses of transport behaviors of ions and water through MSD indicates that the diffusion of the uranyl ion is much less as compared to that of the water molecules. It is also observed that the dynamical behavior of water molecules gets modified due to the presence of uranyl ion. The effect of increase in concentration of uranyl ions on the structure and dynamics of water molecules is also studied.

  7. Dehydration of Uranyl Nitrate Hexahydrate to Uranyl Nitrate Trihydrate under Ambient Conditions as Observed via Dynamic Infrared Reflectance Spectroscopy

    SciTech Connect (OSTI)

    Johnson, Timothy J.; Sweet, Lucas E.; Meier, David E.; Mausolf, Edward J.; Kim, Eunja; Weck, Philippe F.; Buck, Edgar C.; McNamara, Bruce K.

    2015-05-22

    the hexahydrate [UO2(NO3)2(H2O)6] (UNH) and the trihydrate [UO2(NO3)2(H2O)3] (UNT) forms. Their stabilities depend on both relative humidity and temperature. Both phases have previously been studied by infrared transmission spectroscopy, but the data were limited by both instrumental resolution and the ability to prepare the samples as pellets without desiccating it. We report time-resolved infrared (IR) measurements using an integrating sphere that allow us to observe the transformation from the hexahydrate to the trihydrate simply by flowing dry nitrogen gas over the sample. Hexahydrate samples were prepared and confirmed via known XRD patterns, then measured in reflectance mode. The hexahydrate has a distinct uranyl asymmetric stretch band at 949.0 cm-1 that shifts to shorter wavelengths and broadens as the sample dehydrates and recrystallizes to the trihydrate, first as a blue edge shoulder but ultimately resulting in a doublet band with reflectance peaks at 966 and 957 cm-1. The data are consistent with transformation from UNH to UNT since UNT has two non-equivalent UO22+ sites. The dehydration of UO2(NO3)2(H2O)6 to UO2(NO3)2(H2O)3 is both a morphological and structural change that has the lustrous lime green crystals changing to the dull greenish yellow of the trihydrate. Crystal structures and phase transformation were confirmed theoretically using DFT calculations and experimentally via microscopy methods. Both methods showed a transformation with two distinct sites for the uranyl cation in the trihydrate, as opposed to a single crystallographic site in the hexahydrate.

  8. ARRAYS OF BOTTLES OF PLUTONIUM NITRATE SOLUTION

    SciTech Connect (OSTI)

    Margaret A. Marshall

    2012-09-01

    In October and November of 1981 thirteen approaches-to-critical were performed on a remote split table machine (RSTM) in the Critical Mass Laboratory of Pacific Northwest Laboratory (PNL) in Richland, Washington using planar arrays of polyethylene bottles filled with plutonium (Pu) nitrate solution. Arrays of up to sixteen bottles were used to measure the critical number of bottles and critical array spacing with a tight fitting Plexiglas reflector on all sides of the arrays except the top. Some experiments used Plexiglas shells fitted around each bottles to determine the effect of moderation on criticality. Each bottle contained approximately 2.4 L of Pu(NO3)4 solution with a Pu content of 105 g Pu/L and a free acid molarity H+ of 5.1. The plutonium was of low 240Pu (2.9 wt.%) content. These experiments were sponsored by Rockwell Hanford Operations because of the lack of experimental data on the criticality of arrays of bottles of Pu solution such as might be found in storage and handling at the Purex Facility at Hanford. The results of these experiments were used to provide benchmark data to validate calculational codes used in criticality safety assessments of [the] plant configurations (Ref. 1). Data for this evaluation were collected from the published report (Ref. 1), the approach to critical logbook, the experimenters logbook, and communication with the primary experimenter, B. Michael Durst. Of the 13 experiments preformed 10 were evaluated. One of the experiments was not evaluated because it had been thrown out by the experimenter, one was not evaluated because it was a repeat of another experiment and the third was not evaluated because it reported the critical number of bottles as being greater than 25. Seven of the thirteen evaluated experiments were determined to be acceptable benchmark experiments. A similar experiment using uranyl nitrate was benchmarked as U233-SOL-THERM-014.

  9. Observation of Radiolytic Field Alteration of the Uranyl Cation in Bicarbonate Solution

    SciTech Connect (OSTI)

    Snow, Lanee A.; McNamara, Bruce K.; Sinkov, Sergey I.; Cho, Herman M.; Friese, Judah I.

    2006-12-01

    In previous work we demonstrated that radiolysis of uranyl tris carbonate in near neutral pH to alkaline carbonate solutions, could be followed by 13C NMR. Radiolysis of the complex produced novel uranyl peroxo carbonate solution state species, whose structures depended on the pH and radiolytic dose rate. In this work, we investigate speciation of the uranyl carbonate trimer which is predominant in bicarbonate solution near pH 5.9. We observe radiolytically derived speciation to different mixed peroxy carbonate species than seen in the higher pH solutions. Auto radiolysis of uranium (VI) carbonate solutions between pH 5.9 and 7.2 is shown to alter the uranium speciation over relatively short periods of time and was followed by 13C NMR and visible spectrophotometry, using dissolved 233(UO2)3(CO3)6 6- both as the radiolysis source (D= 14.9 Gy/hr) and as a trap for the newly formed hydrogen peroxide. Direct addition of hydrogen peroxide to solutions of the uranyl-carbonate trimer is shown to reproduce the 13 C NMR signatures of the complexe(s) formed by radiolysis, but additionally a variety of new complexes are revealed. Ratios of H2O2/trimer < 1.5 produced a uranyl peroxo carbonate adduct, that is shown to be common to the radiolytically produced species. Ratios of H2O2/ trimer >1 resulted in formation of stable higher order peroxo carbonate complexes. The 13C NMR signatures and visible spectra of these complexes are described here. Rigorous characterization of the species is an ongoing effort.

  10. Process for decomposing nitrates in aqueous solution

    DOE Patents [OSTI]

    Haas, Paul A. (Knoxville, TN)

    1980-01-01

    This invention is a process for decomposing ammonium nitrate and/or selected metal nitrates in an aqueous solution at an elevated temperature and pressure. Where the compound to be decomposed is a metal nitrate (e.g., a nuclear-fuel metal nitrate), a hydroxylated organic reducing agent therefor is provided in the solution. In accordance with the invention, an effective proportion of both nitromethane and nitric acid is incorporated in the solution to accelerate decomposition of the ammonium nitrate and/or selected metal nitrate. As a result, decomposition can be effected at significantly lower temperatures and pressures, permitting the use of system components composed of off-the-shelf materials, such as stainless steel, rather than more costly materials of construction. Preferably, the process is conducted on a continuous basis. Fluid can be automatically vented from the reaction zone as required to maintain the operating temperature at a moderate value--e.g., at a value in the range of from about 130.degree.-200.degree. C.

  11. Time-Resolved Infrared Reflectance Studies of the Dehydration-Induced Transformation of Uranyl Nitrate Hexahydrate to the Trihydrate Form

    SciTech Connect (OSTI)

    Johnson, Timothy J.; Sweet, Lucas E.; Meier, David E.; Mausolf, Edward J.; Kim, Eunja; Weck, Philippe F.; Buck, Edgar C.; McNamara, Bruce K.

    2015-10-01

    Uranyl nitrate is a key species in the nuclear fuel cycle. However, this species is known to exist in different states of hydration, including the hexahydrate ([UO2(NO3)2(H2O)6] often called UNH), the trihydrate [UO2(NO3)2(H2O)3 or UNT], and in very dry environments the dihydrate form [UO2(NO3)2(H2O)2]. Their relative stabilities depend on both water vapor pressure and temperature. In the 1950s and 1960s the different phases were studied by infrared transmission spectroscopy, but were limited both by instrumental resolution and by the ability to prepare the samples for transmission. We have revisited this problem using time-resolved reflectance spectroscopy, which requires no sample preparation and allows dynamic analysis while the sample is exposed to a flow of N2 gas. Samples of known hydration state were prepared and confirmed via X-ray diffraction patterns of known species. In reflectance mode the hexahydrate UO2(NO3)2(H2O)6 has a distinct uranyl asymmetric stretch band at 949.0 cm-1 that shifts to shorter wavelengths and broadens as the sample desiccates and recrystallizes to the trihydrate, first as a shoulder growing in on the blue edge but ultimately results in a doublet band with reflectance peaks at 966 and 957 cm-1. The data are consistent with transformation from UNH to UNT as UNT has two inequivalent UO22+ sites. The dehydration of UO2(NO3)2(H2O)6 to UO2(NO3)2(H2O)3 is both a structural and morphological change that has the lustrous lime green UO2(NO3)2(H2O)6 crystals changing to the matte greenish yellow of the trihydrate solid. The phase transformation and crystal structures were confirmed by density functional theory calculations and optical microscopy methods, both of which showed a transformation with two distinct sites for the uranyl cation in the trihydrate, with but one in the hexahydrate.

  12. Time-resolved infrared reflectance studies of the dehydration-induced transformation of uranyl nitrate hexahydrate to the trihydrate form

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Johnson, Timothy J.; Sweet, Lucas E.; Meier, David E.; Edward J. Mausolf; Kim, Eunja; Weck, Philippe F.; Buck, Edgar C.; Bruce K. McNamara

    2015-09-08

    Uranyl nitrate is a key species in the nuclear fuel cycle. However, this species is known to exist in different states of hydration, including the hexahydrate ([UO2(NO3)2(H2O)6] often called UNH), the trihydrate [UO2(NO3)2(H2O)3 or UNT], and in very dry environments the dihydrate form [UO2(NO3)2(H2O)2]. Their relative stabilities depend on both water vapor pressure and temperature. In the 1950s and 1960s, the different phases were studied by infrared transmission spectroscopy but were limited both by instrumental resolution and by the ability to prepare the samples for transmission. We have revisited this problem using time-resolved reflectance spectroscopy, which requires no sample preparationmore » and allows dynamic analysis while the sample is exposed to a flow of N2 gas. Samples of known hydration state were prepared and confirmed via X-ray diffraction patterns of known species. In reflectance mode the hexahydrate UO2(NO3)2(H2O)6 has a distinct uranyl asymmetric stretch band at 949.0 cm–1 that shifts to shorter wavelengths and broadens as the sample desiccates and recrystallizes to the trihydrate, first as a shoulder growing in on the blue edge but ultimately results in a doublet band with reflectance peaks at 966 and 957 cm–1. The data are consistent with transformation from UNH to UNT as UNT has two inequivalent UO22+ sites. The dehydration of UO2(NO3)2(H2O)6 to UO2(NO3)2(H2O)3 is both a structural and morphological change that has the lustrous lime green UO2(NO3)2(H2O)6 crystals changing to the matte greenish yellow of the trihydrate solid. As a result, the phase transformation and crystal structures were confirmed by density functional theory calculations and optical microscopy methods, both of which showed a transformation with two distinct sites for the uranyl cation in the trihydrate, with only one in the hexahydrate.« less

  13. Time-resolved infrared reflectance studies of the dehydration-induced transformation of uranyl nitrate hexahydrate to the trihydrate form

    SciTech Connect (OSTI)

    Johnson, Timothy J.; Sweet, Lucas E.; Meier, David E.; Edward J. Mausolf; Kim, Eunja; Weck, Philippe F.; Buck, Edgar C.; Bruce K. McNamara

    2015-09-08

    Uranyl nitrate is a key species in the nuclear fuel cycle. However, this species is known to exist in different states of hydration, including the hexahydrate ([UO2(NO3)2(H2O)6] often called UNH), the trihydrate [UO2(NO3)2(H2O)3 or UNT], and in very dry environments the dihydrate form [UO2(NO3)2(H2O)2]. Their relative stabilities depend on both water vapor pressure and temperature. In the 1950s and 1960s, the different phases were studied by infrared transmission spectroscopy but were limited both by instrumental resolution and by the ability to prepare the samples for transmission. We have revisited this problem using time-resolved reflectance spectroscopy, which requires no sample preparation and allows dynamic analysis while the sample is exposed to a flow of N2 gas. Samples of known hydration state were prepared and confirmed via X-ray diffraction patterns of known species. In reflectance mode the hexahydrate UO2(NO3)2(H2O)6 has a distinct uranyl asymmetric stretch band at 949.0 cm–1 that shifts to shorter wavelengths and broadens as the sample desiccates and recrystallizes to the trihydrate, first as a shoulder growing in on the blue edge but ultimately results in a doublet band with reflectance peaks at 966 and 957 cm–1. The data are consistent with transformation from UNH to UNT as UNT has two inequivalent UO22+ sites. The dehydration of UO2(NO3)2(H2O)6 to UO2(NO3)2(H2O)3 is both a structural and morphological change that has the lustrous lime green UO2(NO3)2(H2O)6 crystals changing to the matte greenish yellow of the trihydrate solid. As a result, the phase transformation and crystal structures were confirmed by density functional theory calculations and optical microscopy methods, both of which showed a transformation with two distinct sites for the uranyl cation in the trihydrate, with only one in the hexahydrate.

  14. Method for photochemical reduction of uranyl nitrate by tri-N-butyl phosphate and application of this method to nuclear fuel reprocessing

    DOE Patents [OSTI]

    De Poorter, Gerald L. (Los Alamos, NM); Rofer-De Poorter, Cheryl K. (Los Alamos, NM)

    1978-01-01

    Uranyl ion in solution in tri-n-butyl phosphate is readily photochemically reduced to U(IV). The product U(IV) may effectively be used in the Purex process for treating spent nuclear fuels to reduce Pu(IV) to Pu(III). The Pu(III) is readily separated from uranium in solution in the tri-n-butyl phosphate by an aqueous strip.

  15. Method for improved decomposition of metal nitrate solutions

    DOE Patents [OSTI]

    Haas, P.A.; Stines, W.B.

    1981-01-21

    A method for co-conversion of aqueous solutions of one or more heavy metal nitrates is described, wherein thermal decomposition within a temperature range of about 300 to 800/sup 0/C is carried out in the presence of about 50 to 500% molar concentration of ammonium nitrate to total metal.

  16. Method for improved decomposition of metal nitrate solutions

    DOE Patents [OSTI]

    Haas, Paul A. (Knoxville, TN); Stines, William B. (Knoxville, TN)

    1983-10-11

    A method for co-conversion of aqueous solutions of one or more heavy metal nitrates wherein thermal decomposition within a temperature range of about 300.degree. to 800.degree. C. is carried out in the presence of about 50 to 500% molar concentration of ammonium nitrate to total metal.

  17. Design and Construction of Experiment for Direct Electron Irradiation of Uranyl Sulfate Solution: Bubble Formation and Thermal Hydraulics Studies

    SciTech Connect (OSTI)

    Chemerisov, Sergey; Gromov, Roman; Makarashvili, Vakho; Heltemes, Thad; Sun, Zaijing; Wardle, Kent E.; Bailey, James; Quigley, Kevin; Stepinski, Dominique; Vandegrift, George

    2014-10-01

    Argonne is assisting SHINE Medical Technologies in developing SHINE, a system for producing fission-product 99Mo using a D/T-accelerator to produce fission in a non-critical target solution of aqueous uranyl sulfate. We have developed an experimental setup for studying thermal-hydraulics and bubble formation in the uranyl sulfate solution to simulate conditions expected in the SHINE target solution during irradiation. A direct electron beam from the linac accelerator will be used to irradiate a 20 L solution (sector of the solution vessel). Because the solution will undergo radiolytic decomposition, we will be able to study bubble formation and dynamics and effects of convection and temperature on bubble behavior. These experiments will serve as a verification/ validation tool for the thermal-hydraulic model. Utilization of the direct electron beam for irradiation allows homogeneous heating of a large solution volume and simplifies observation of the bubble dynamics simultaneously with thermal-hydraulic data collection, which will complement data collected during operation of the miniSHINE experiment. Irradiation will be conducted using a 30-40 MeV electron beam from the high-power linac accelerator. The total electron-beam power will be 20 kW, which will yield a power density on the order of 1 kW/L. The solution volume will be cooled on the front and back surfaces and central tube to mimic the geometry of the proposed SHINE solution vessel. Also, multiple thermocouples will be inserted into the solution vessel to map thermal profiles. The experimental design is now complete, and installation and testing are in progress.

  18. Critical experiments with mixed plutonium-uranium nitrate solutions having

    Office of Scientific and Technical Information (OSTI)

    Pu:(Pu + U) ratios greater than 0.5 (Technical Report) | SciTech Connect Critical experiments with mixed plutonium-uranium nitrate solutions having Pu:(Pu + U) ratios greater than 0.5 Citation Details In-Document Search Title: Critical experiments with mixed plutonium-uranium nitrate solutions having Pu:(Pu + U) ratios greater than 0.5 × You are accessing a document from the Department of Energy's (DOE) SciTech Connect. This site is a product of DOE's Office of Scientific and Technical

  19. The radiation induced chemistry of uranyl cation in aqueous carbonate bicarbonate solutions as followed by NMR spectroscopy

    SciTech Connect (OSTI)

    McNamara, Bruce K.; Snow, Lanee A.; Soderquist, Chuck Z.; Sinkov, Sergei I.; Cho, Herman M.; Friese, Judah I.

    2006-05-01

    Alpha radiation induced formation of hydrogen peroxide in carbonate ?bicarbonate media was followed by 13C NMR using dissolved [233UO2(13CO3)3]4- as the alpha source (Dalpha= 12.1 Gy/hr). Between the pH region between 5.9 and 11.6 hydrogen peroxide causes a varied speciation of the uranyl carbonates that is a function of the uranium, carbonate and the hydrogen peroxide concentrations. It is shown that the speciation of the peroxy carbonates (or other species) formed in solution by titration with hydrogen peroxide are common to those formed by hydrogen peroxide generated by radiolysis. The radiolysis experiment was carried out above pH = 9.96 to minimize the loss of 13CO2 over a 2800 hr period. Radiolytic generation of hydrogen peroxide was followed by formation of a uranyl peroxy carbonate complex and complex formation accelerated for about 1200 hours. Complex formation was observed to terminate at a concentration between 1x10-4 and 5x10-4 M. It is assumed that either a steady state H2O2 production rate was established in solution or that some limiting feature of the experiment was responsible for slowing the yield of product.

  20. Experimental Results for Direct Electron Irradaition of a Uranyl Sulfate Solution: Bubble Formation and Thermal Hydraulics Studies

    SciTech Connect (OSTI)

    Chemerisov, Sergey; Gromov, R.; Makarashvili, Vakhtang; Heltemes, Thad; Sun, Zaijing; Wardle, Kent E.; Bailey, James; Stepinski, Dominique; Jerden, James; Vandegrift, George F.

    2015-01-30

    In support of the development of accelerator-driven production of fission product Mo-99 as proposed by SHINE Medical Technologies, a 35 MeV electron linac was used to irradiate depleted-uranium (DU) uranyl sulfate dissolved in pH 1 sulfuric acid at average power densities of 6 kW, 12 kW, and 15 kW. During these irradiations, gas bubbles were generated in the solution due to the radiolytic decomposition of water molecules in the solution. Multiple video cameras were used to record the behavior of bubble generation and transport in the solution. Seven six-channel thermocouples were used to record temperature gradients in the solution from self-heating. Measurements of hydrogen and oxygen concentrations in a helium sweep gas were recorded by a gas chromatograph to estimate production rates during irradiation. These data are being used to validate a computational fluid dynamics (CFD) model of the experiment that includes multiphase flow and a custom bubble injection model for the solution region.

  1. Toluene nitration in irradiated nitric acid and nitrite solution

    SciTech Connect (OSTI)

    Gracy Elias; Bruce J. Mincher; Stephen P. Mezyk; Jim Muller; Leigh R. Martin

    2011-04-01

    The kinetics, mechanisms, and stable products produced for the aryl alkyl mild ortho-para director - toluene, in irradiated nitric acid and neutral nitrite solutions were investigated using ?, and pulse radiolysis. Electron pulse radiolysis was used to determine the bimolecular rate constants for the reaction of toluene with different transient species produced by irradiation. HPLC with UV detection was primarily used to assess the stable reaction products. GC-MS and LC-MS were used to confirm the results from HPLC. Free-radical nitration reaction products were found in irradiated acidic and neutral media. In acidic medium, the ring substitution and side chain substitution and oxidation produced different nitro products. In ring substitution, nitrogen oxide radicals were added mainly to hydroxyl radical-produced cyclohexadienyl radical, and in side chain substitution they were added to the carbon-centered benzyl radical produced by H-atom abstraction. In neutral nitrite toluene solution, radiolytic ring nitration products approached a statistically random distribution, suggesting a free-radical reaction involving addition of the NO2 radical.

  2. Solution High-Energy Burst Assembly (SHEBA) results from subprompt critical experiments with uranyl fluoride fuel

    SciTech Connect (OSTI)

    Cappiello, C.C.; Butterfield, K.B.; Sanchez, R.G.; Bounds, J.A.; Kimpland, R.H.; Damjanovich, R.P.; Jaegers, P.J.

    1997-08-01

    Experiments were performed to measure a variety of parameters for SHEBA: behavior of the facility during transient and steady-state operation; characteristics of the SHEBA fuel; delayed-critical solution height vs solution temperature; initial reactor period and reactivity vs solution height; calibration of power level vs reactor power instrumentation readings; flux profile in SHEBA; radiation levels and neutron spectra outside the assembly for code verification and criticality alarm and dosimetry purposes; and effect on reactivity of voids in the fuel.

  3. Optical apparatus and method for sensing uranyl

    DOE Patents [OSTI]

    Baylor, L.C.; Buchanan, B.R.

    1994-01-01

    An optical sensing device for uranyl and other substances, a method for making an optical sensing device and a method for chemically binding uranyl and other indicators to glass, quartz, cellulose and similar substrates. The indicator, such as arsenazo III, is immobilized on the substrate using a chemical binding process. The immobilized arsenazo III causes uranyl from a fluid sample to bind irreversibly to the substrate at its active sites, thus causing absorption of a portion of light transmitted through the substrate. Determination of the amount of light absorbed, using conventional means, yields the concentration of uranyl present in the sample fluid. The binding of uranyl on the substrate can be reversed by subsequent exposure of the substrate to a solution of 2,6-pyridinedicarboxylic acid. The chemical binding process is suitable for similarly binding other indicators, such as bromocresol green.

  4. Composition for detecting uranyl

    DOE Patents [OSTI]

    Baylor, L.C.; Stephens, S.M.

    1994-01-01

    The present invention relates to an indicator composition for use in spectrophotometric detection of a substance in a solution, and a method for making the composition. Useful indicators are sensitive to the particular substance being measured, but are unaffected by the fluid and other chemical species that may be present in the fluid. Optical indicators are used to measure the uranium concentration of process solutions in facilities for extracting uranium from ores, production of nuclear fuels, and reprocessing of irradiated fuels. The composition comprises an organohalide covalently bonded to an indicator for the substance, in such a manner that the product is itself an indicator that provides increased spectral resolution for detecting the substance. The indicator is preferably arsenazo III and the organohalide is preferably cyanuric chloride. These form a composition that is ideally suited for detecting uranyl.

  5. Combined Extraction of Cesium and Strontium from Akaline Nitrate Solutions

    SciTech Connect (OSTI)

    Delmau, Laetitia Helene; Bonnesen, Peter V; Engle, Nancy L; Haverlock, Tamara; Sloop Jr, Frederick {Fred} V; Moyer, Bruce A

    2006-01-01

    The combined extraction of cesium and strontium from caustic wastes can be achieved by adding a crown ether and a carboxylic acid to the Caustic-Side Solvent Extraction (CSSX) solvent. The ligand 4,4'(5')-di(tert-butyl)cyclohexano-18-crown-6 and one of four different carboxylic acids were combined with the components of the CSSX solvent optimized for the extraction of cesium, allowing for the simultaneous extraction of cesium and strontium from alkaline nitrate media simulating alkaline high level wastes present at the U.S. Department of Energy Savannah River Site. Extraction and stripping experiments were conducted independently and exhibited adequate results for mimicking waste simulant processing through batch contacts. The promising results of these batch tests showed that the system could reasonably be tested on actual waste.

  6. Composition for detecting uranyl

    DOE Patents [OSTI]

    Baylor, Lewis C. (North Augusta, SC); Stephens, Susan M. (Athens, GA)

    1995-01-01

    A composition for detecting the presence and concentration of a substance such as uranyl, comprising an organohalide covalently bonded to an indicator for said substance. The composition has at least one active OH site for forming a complex with the substance to be detected. The composition is made by reacting equimolar amounts of the indicator and the organohalide in a polar organic solvent. The absorbance spectrum of the composition-uranyl complex is shifted with respect to the absorbance spectrum of the indicator-uranyl complex, to provide better spectral resolution for detecting uranyl.

  7. Barium uranyl diphosphonates

    SciTech Connect (OSTI)

    Nelson, Anna-Gay D.; Alekseev, Evgeny V.; Ewing, Rodney C.; Albrecht-Schmitt, Thomas E.

    2012-08-15

    Three Ba{sup 2+}/UO{sub 2}{sup 2+} methylenediphosphonates have been prepared from mild hydrothermal treatment of uranium trioxide, methylendiphosphonic acid (C1P2) with barium hydroxide octahydrate, barium iodate monohydrate, and small aliquots of HF at 200 Degree-Sign C. These compounds, Ba[UO{sub 2}[CH{sub 2}(PO{sub 3}){sub 2}]{center_dot}1.4H{sub 2}O (Ba-1), Ba{sub 3}[(UO{sub 2}){sub 4}(CH{sub 2}(PO{sub 3}){sub 2}){sub 2}F{sub 6}]{center_dot}6H{sub 2}O (Ba-2), and Ba{sub 2}[(UO{sub 2}){sub 2}(CH{sub 2}(PO{sub 3}){sub 2})F{sub 4}]{center_dot}5.75H{sub 2}O (Ba-3) all adopt layered structures based upon linear uranyl groups and disphosphonate molecules. Ba-2 and Ba-3 are similar in that they both have UO{sub 5}F{sub 2} pentagonal bipyramids that are bridged and chelated by the diphosphonate moiety into a two-dimensional zigzag anionic sheet (Ba-2) and a one-dimensional ribbon anionic chain (Ba-3). Ba-1, has a single crystallographically unique uranium metal center where the C1P2 ligand solely bridges to form [UO{sub 2}[CH{sub 2}(PO{sub 3}){sub 2}]{sup 2-} sheets. The interlayer space of the structures is occupied by Ba{sup 2+}, which, along with the fluoride ion, mediates the structure formed and maintains overall charge balance. - Graphical abstract: Illustration of the stacking of the layers in Ba{sub 3}[(UO{sub 2}){sub 4}(CH{sub 2}(PO{sub 3}){sub 2}){sub 2})F{sub 6}]{center_dot}6H{sub 2}O viewed along the c-axis. The structure is constructed from UO{sub 7} pentagonal bipyramidal units, U(1)O{sub 7}=gray, U(2)O{sub 7}=yellow, barium=blue, phosphorus=magenta, fluorine=green, oxygen=red, carbon=black, and hydrogen=light peach. Highlights: Black-Right-Pointing-Pointer The polymerization of the UO{sub 2}{sup 2+} sites to form uranyl dimers leads to structural variations in compounds. Black-Right-Pointing-Pointer Barium cations stitch uranyl diphosphonate anionic layers together, and help mediate structure formation. Black-Right-Pointing-Pointer HF acts as both a mineralizing agent and a ligand.

  8. Modeling of early age loss of lithium ions from pore solution of cementitious systems treated with lithium nitrate

    SciTech Connect (OSTI)

    Kim, Taehwan Olek, Jan

    2015-01-15

    Addition of lithium nitrate admixture to the fresh concrete mixture helps to minimize potential problems related to alkali-silica reaction. For this admixture to function as an effective ASR control measure, it is imperative that the lithium ions remain in the pore solution. However, it was found that about 50% of the originally added lithium ions are removed from the pore solution during early stages of hydration. This paper revealed that the magnitude of the Li{sup +} ion loss is highly dependent on the concentration of Li{sup +} ions in the pore solution and the hydration rate of the cementitious systems. Using these findings, an empirical model has been developed which can predict the loss of Li{sup +} ions from the pore solution during the hydration period. The proposed model can be used to investigate the effects of mixture parameters on the loss of Li{sup +} ions from the pore solution of cementitious system.

  9. Criticality experiments with planar arrays of three-liter bottles containing plutonium nitrate solution

    SciTech Connect (OSTI)

    Durst, B.M.; Clayton, E.D.; Smith, J.H.

    1985-01-01

    The objective of these experiments was to provide benchmark data to validate calculational codes used in critically safety assessments of plant configurations. Arrays containing up to as many as sixteen three-liter bottles filled with plutonium nitrate were used in the experiments. A split-table device was used in the final assembly of the arrays. Ths planar arrays were reflected with close fitting plexiglas on each side and on the bottom but not the top surface. The experiments addressed a number of factors effecting criticality: the critical air gap between bottles in an array of fixed number of bottles, the number of bottles required for criticality if the bottles were touching, and the effect on critical array spacing and critical bottle number due to the insertion of an hydrogeneous substance into the air gap between bottles. Each bottle contained about 2.4l of Pu(NO{sub 3}){sub 4} solution at a Pu concentration of 105g Pu/l, with the {sup 240}Pu content being 2.9 wt% at a free acid molarity H{sup +} of 5.1. After the initial series of experiments were performed with bottles separated by air gaps, plexiglas shells of varying thicknesses were placed around each bottle to investigate how moderation between bottles affects both the number of bottles required for criticality and the critical spacing between each bottle. The minimum of bottles required for criticality was found to be 10.9 bottles, occurring for a square array with bottles in contact. As the bottles were spaced apart, the critical number increased. For sixteen bottles in a square array, the critical separation between surfaces in both x and y direction was 0.96 cm. The addition of plexiglas around each bottle decreased the critical bottle number, compared to those separated in air, but the critical bottle number, even with interstitial plastic in place was always greater than 10.9 bottles. The most reactive configuration was a tightly packed array of bottles with no intervening material.

  10. Alkali metal nitrate purification

    DOE Patents [OSTI]

    Fiorucci, Louis C. (Hamden, CT); Morgan, Michael J. (Guilford, CT)

    1986-02-04

    A process is disclosed for removing contaminants from impure alkali metal nitrates containing them. The process comprises heating the impure alkali metal nitrates in solution form or molten form at a temperature and for a time sufficient to effect precipitation of solid impurities and separating the solid impurities from the resulting purified alkali metal nitrates. The resulting purified alkali metal nitrates in solution form may be heated to evaporate water therefrom to produce purified molten alkali metal nitrates suitable for use as a heat transfer medium. If desired, the purified molten form may be granulated and cooled to form discrete solid particles of purified alkali metal nitrates.

  11. Gas Phase Uranyl Activation: Formation of a Uranium Nitrosyl Complex from Uranyl Azide

    SciTech Connect (OSTI)

    Gong, Yu; De Jong, Wibe A.; Gibson, John K.

    2015-05-13

    Activation of the oxo bond of uranyl, UO22+, was achieved by collision induced dissociation (CID) of UO2(N3)Cl2 in a quadrupole ion trap mass spectrometer. The gas phase complex UO2(N3)Cl2 was produced by electrospray ionization of solutions of UO2Cl2 and NaN3. CID of UO2(N3)Cl2 resulted in the loss of N2 to form UO(NO)Cl2, in which the inert uranyl oxo bond has been activated. Formation of UO2Cl2 via N3 loss was also observed. Density functional theory computations predict that the UO(NO)Cl2 complex has nonplanar Cs symmetry and a singlet ground state. Analysis of the bonding of the UO(NO)Cl2 complex shows that the side-on bonded NO moiety can be considered as NO3, suggesting a formal oxidation state of U(VI). Activation of the uranyl oxo bond in UO2(N3)Cl2 to form UO(NO)Cl2 and N2 was computed to be endothermic by 169 kJ/mol, which is energetically more favorable than formation of NUOCl2 and UO2Cl2. The observation of UO2Cl2 during CID is most likely due to the absence of an energy barrier for neutral ligand loss.

  12. Purification of alkali metal nitrates

    DOE Patents [OSTI]

    Fiorucci, Louis C. (Hamden, CT); Gregory, Kevin M. (Woodridge, IL)

    1985-05-14

    A process is disclosed for removing heavy metal contaminants from impure alkali metal nitrates containing them. The process comprises mixing the impure nitrates with sufficient water to form a concentrated aqueous solution of the impure nitrates, adjusting the pH of the resulting solution to within the range of between about 2 and about 7, adding sufficient reducing agent to react with heavy metal contaminants within said solution, adjusting the pH of the solution containing reducing agent to effect precipitation of heavy metal impurities and separating the solid impurities from the resulting purified aqueous solution of alkali metal nitrates. The resulting purified solution of alkali metal nitrates may be heated to evaporate water therefrom to produce purified molten alkali metal nitrate suitable for use as a heat transfer medium. If desired, the purified molten form may be granulated and cooled to form discrete solid particles of alkali metal nitrates.

  13. Selectivity in ligand binding to uranyl compounds: A synthetic, structural, thermodynamic and computational study

    SciTech Connect (OSTI)

    Arnold, John

    2015-01-21

    The uranyl cation (UO??) is the most abundant form of uranium on the planet. It is estimated that 4.5 billion tons of uranium in this form exist in sea water. The ability to bind and extract the uranyl cation from aqueous solution while separating it from other elements would provide a limitless source of nuclear fuel. A large body of research concerns the selective recognition and extraction of uranyl. A stable molecule, the cation has a linear O=U=O geometry. The short U-O bonds (1.78 ) arise from the combination of uranium 5f/6d and oxygen 2p orbitals. Due to the oxygen moieties being multiply bonded, these sites were not thought to be basic enough for Lewis acidic coordination to be a viable approach to sequestration.

  14. Nitrate reduction

    DOE Patents [OSTI]

    Dziewinski, Jacek J. (Los Alamos, NM); Marczak, Stanislaw (Los Alamos, NM)

    2000-01-01

    Nitrates are reduced to nitrogen gas by contacting the nitrates with a metal to reduce the nitrates to nitrites which are then contacted with an amide to produce nitrogen and carbon dioxide or acid anions which can be released to the atmosphere. Minor amounts of metal catalysts can be useful in the reduction of the nitrates to nitrites. Metal salts which are formed can be treated electrochemically to recover the metals.

  15. Process for reducing aqueous nitrate to ammonia

    DOE Patents [OSTI]

    Mattus, Alfred J. (Oak Ridge, TN)

    1993-01-01

    Powdered aluminum is added to a nitrate-containing alkaline, aqueous solution to reduce the nitrate and/or nitrite to ammonia and co-produce a sinterable ceramic product.

  16. Process for reducing aqueous nitrate to ammonia

    DOE Patents [OSTI]

    Mattus, A.J.

    1993-11-30

    Powdered aluminum is added to a nitrate-containing alkaline, aqueous solution to reduce the nitrate and/or nitrite to ammonia and co-produce a sinterable ceramic product. 3 figures.

  17. Analysis of Tank 43H Samples at the Conclusion of Uranyl Carbonate Addition

    SciTech Connect (OSTI)

    Oji, L.N.

    2002-10-15

    Tank 43H serves as the feed Tank to the 2H evaporator. In the months of July and August 2001, about 21,000 gallons of a depleted uranyl carbonate solution were added to Tank 43H and agitated with two Flygt mixers. The depleted uranium addition served to decrease the U-235 enrichment in the Tank 43H supernate so that the supernate could be evaporated with no risk of accumulating enriched uranium.

  18. Sequestering Uranium from Seawater: Binding Strength and Modes of Uranyl

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

    Complexes with Glutarimidedioxime Sequestering Uranium from Seawater: Binding Strength and Modes of Uranyl Complexes with Glutarimidedioxime Sequestering Uranium from Seawater: Binding Strength and Modes of Uranyl Complexes with Glutarimidedioxime Print Sunday, 14 October 2012 00:00 The ocean is an important source of uranium if it can be extracted economically. Extraction of uranium from seawater is very challenging, not only because it is in an extremely low concentration, but also because

  19. Method of precipitating uranium from an aqueous solution and/or sediment

    DOE Patents [OSTI]

    Tokunaga, Tetsu K; Kim, Yongman; Wan, Jiamin

    2013-08-20

    A method for precipitating uranium from an aqueous solution and/or sediment comprising uranium and/or vanadium is presented. The method includes precipitating uranium as a uranyl vanadate through mixing an aqueous solution and/or sediment comprising uranium and/or vanadium and a solution comprising a monovalent or divalent cation to form the corresponding cation uranyl vanadate precipitate. The method also provides a pathway for extraction of uranium and vanadium from an aqueous solution and/or sediment.

  20. WIPP Nitrate Updates 2015

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

    5 WIPP Nitrate Salt Bearing Waste Container Isolation Plan Implementation Update, July 23, 2015 Waste Isolation Pilot Plant EPA I.D. Number: NM4890139088-TSDF WIPP Nitrate Salt...

  1. Energetic Material - Electro Nitration - Energy Innovation Portal

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

    Electro Nitration Idaho National Laboratory Contact INL About This Technology Technology Marketing SummaryINL has developed an improved method of nitrating a nitro compound by oxidizing a chemical mediator in the presence of a voltage in order to produce an oxidizing agent. Then, the agent reacts with a nitro compound and ion source in a solution in order to form a geminaldinitro compound. The electrochemical synthesis of geminaldinitro results in the formation of a nitro compound that may be

  2. Predicting Stability Constants for Uranyl Complexes Using Density Functional Theory

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Vukovic, Sinisa; Hay, Benjamin P.; Bryantsev, Vyacheslav S.

    2015-04-02

    The ability to predict the equilibrium constants for the formation of 1:1 uranyl:ligand complexes (log K1 values) provides the essential foundation for the rational design of ligands with enhanced uranyl affinity and selectivity. We also use density functional theory (B3LYP) and the IEFPCM continuum solvation model to compute aqueous stability constants for UO22+ complexes with 18 donor ligands. Theoretical calculations permit reasonably good estimates of relative binding strengths, while the absolute log K1 values are significantly overestimated. Accurate predictions of the absolute log K1 values (root mean square deviation from experiment < 1.0 for log K1 values ranging from 0more » to 16.8) can be obtained by fitting the experimental data for two groups of mono and divalent negative oxygen donor ligands. The utility of correlations is demonstrated for amidoxime and imide dioxime ligands, providing a useful means of screening for new ligands with strong chelate capability to uranyl.« less

  3. Predicting Stability Constants for Uranyl Complexes Using Density Functional Theory

    SciTech Connect (OSTI)

    Vukovic, Sinisa; Hay, Benjamin P.; Bryantsev, Vyacheslav S.

    2015-04-02

    The ability to predict the equilibrium constants for the formation of 1:1 uranyl:ligand complexes (log K1 values) provides the essential foundation for the rational design of ligands with enhanced uranyl affinity and selectivity. We also use density functional theory (B3LYP) and the IEFPCM continuum solvation model to compute aqueous stability constants for UO22+ complexes with 18 donor ligands. Theoretical calculations permit reasonably good estimates of relative binding strengths, while the absolute log K1 values are significantly overestimated. Accurate predictions of the absolute log K1 values (root mean square deviation from experiment < 1.0 for log K1 values ranging from 0 to 16.8) can be obtained by fitting the experimental data for two groups of mono and divalent negative oxygen donor ligands. The utility of correlations is demonstrated for amidoxime and imide dioxime ligands, providing a useful means of screening for new ligands with strong chelate capability to uranyl.

  4. Thermochemical nitrate destruction

    DOE Patents [OSTI]

    Cox, John L. (Richland, WA); Hallen, Richard T. (Richland, WA); Lilga, Michael A. (Richland, WA)

    1992-01-01

    A method is disclosed for denitrification of nitrates and nitrates present in aqueous waste streams. The method comprises the steps of (1) identifying the concentration nitrates and nitrites present in a waste stream, (2) causing formate to be present in the waste stream, (3) heating the mixture to a predetermined reaction temperature from about 200.degree. C. to about 600.degree. C., and (4) holding the mixture and accumulating products at heated and pressurized conditions for a residence time, thereby resulting in nitrogen and carbon dioxide gas, and hydroxides, and reducing the level of nitrates and nitrites to below drinking water standards.

  5. Conversion of actinide and RE oxides into nitrates and their recovery into fluids

    SciTech Connect (OSTI)

    Bondin, V.V.; Bychkov, S.I.; Efremov, I.G.; Revenko, Y.A.; Babain, V.A.; Murzin, A.A.; Romanovsky, V.N; Fedorov, Y.S.; Shadrin, A.Y.; Ryabkova, N.V.; Li, E.N.

    2007-07-01

    The conditions for uranium oxides completely convert into uranyl nitrate hexahydrate in nitrogen tetra-oxide media (75 deg. C, 0,5-3,0 MPa, [UO{sub x}]:[H{sub 2}O]:[NO{sub 2}]=1:8:6) were found out. The conversion of Pu contained simulator of oxide spent nuclear fuel of thermal reactors was successfully demonstrated. The possibility of uranium recovery up to 95% from TR SNF without plutonium separation from FP is practically showed, what corresponds with Non-proliferation Treaty. (authors)

  6. Time-dependent water dynamics in hydrated uranyl fluoride

    SciTech Connect (OSTI)

    Miskowiec, Andrew J.; Anderson, Brian B.; Herwig, Kenneth W.; Huq, Ashfia; Mamontov, Eugene; Rondinone, Adam; Trowbridge, Lee D.

    2015-09-15

    In this study, uranyl fluoride is a three-layer, hexagonal structure with significant stacking disorder in the c-direction. It supports a range of unsolved thermodynamic hydrates with 02.5 water molecules per uranium atom, and perhaps more. However, the relationship between water, hydrate crystal structures, and thermodynamic results, collectively representing the chemical pathway through these hydrate structures, has not been sufficiently elucidated. We used high-resolution quasielastic neutron scattering to study the dynamics of water in partially hydrated uranyl fluoride powder over the course of 4 weeks under closed conditions. The spectra are composed of two quasielastic components: one is associated with translational diffusive motion of water that is approximately five to six times slower than bulk water, and the other is a slow (on the order of 2300 ps), spatially bounded water motion. The translational component represents water diffusing between the weakly bonded layers in the crystal, while the bounded component may represent water trapped in subnanometre pockets formed by the space between uranium-centred polymerisation units. Complementary neutron diffraction measurements do not show any significant structural changes, suggesting that a chemical conversion of the material does not occur in the thermodynamically isolated system on this timescale.

  7. Time-dependent water dynamics in hydrated uranyl fluoride

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Miskowiec, Andrew J.; Anderson, Brian B.; Herwig, Kenneth W.; Huq, Ashfia; Mamontov, Eugene; Rondinone, Adam; Trowbridge, Lee D.

    2015-09-15

    In this study, uranyl fluoride is a three-layer, hexagonal structure with significant stacking disorder in the c-direction. It supports a range of unsolved ‘thermodynamic’ hydrates with 0–2.5 water molecules per uranium atom, and perhaps more. However, the relationship between water, hydrate crystal structures, and thermodynamic results, collectively representing the chemical pathway through these hydrate structures, has not been sufficiently elucidated. We used high-resolution quasielastic neutron scattering to study the dynamics of water in partially hydrated uranyl fluoride powder over the course of 4 weeks under closed conditions. The spectra are composed of two quasielastic components: one is associated with translationalmore » diffusive motion of water that is approximately five to six times slower than bulk water, and the other is a slow (on the order of 2–300 ps), spatially bounded water motion. The translational component represents water diffusing between the weakly bonded layers in the crystal, while the bounded component may represent water trapped in subnanometre ‘pockets’ formed by the space between uranium-centred polymerisation units. Complementary neutron diffraction measurements do not show any significant structural changes, suggesting that a chemical conversion of the material does not occur in the thermodynamically isolated system on this timescale.« less

  8. Thermochemical nitrate destruction

    DOE Patents [OSTI]

    Cox, J.L.; Hallen, R.T.; Lilga, M.A.

    1992-06-02

    A method is disclosed for denitrification of nitrates and nitrites present in aqueous waste streams. The method comprises the steps of (1) identifying the concentration nitrates and nitrites present in a waste stream, (2) causing formate to be present in the waste stream, (3) heating the mixture to a predetermined reaction temperature from about 200 C to about 600 C, and (4) holding the mixture and accumulating products at heated and pressurized conditions for a residence time, thereby resulting in nitrogen and carbon dioxide gas, and hydroxides, and reducing the level of nitrates and nitrites to below drinking water standards.

  9. WIPP Nitrate Updates 2014

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

    Update, December 4, 2014 Waste Isolation Pilot Plant EPA I.D. Number: NM4890139088-TSDF Jose R. FrancoCBFO and Robert L. McQuinnNWP dated December 5, 2014 WIPP Nitrate Salt...

  10. New three-dimensional inorganic frameworks based on the uranophane-type sheet in monoamine templated uranyl-vanadates

    SciTech Connect (OSTI)

    Jouffret, Laurent; Shao Zhenmian

    2010-10-15

    Seven new uranyl vanadates with mono-protonated amine or tetramethylammonium used as structure directing cations, (C{sub 2}NH{sub 8}){sub 2{l_brace}}[(UO{sub 2})(H{sub 2}O)][(UO{sub 2})(VO{sub 4})]{sub 4{r_brace}}.H{sub 2}O (DMetU5V4) (C{sub 2}NH{sub 8}){l_brace}[(UO{sub 2})(H{sub 2}O){sub 2}][(UO{sub 2})(VO{sub 4})]{sub 3{r_brace}}.H{sub 2}O (DMetU4V3), (C{sub 5}NH{sub 6}){sub 2{l_brace}}[(UO{sub 2})(H{sub 2}O)][(UO{sub 2})(VO{sub 4})]{sub 4{r_brace}}.H{sub 2}O (PyrU5V4), (C{sub 3}NH{sub 10}){l_brace}[(UO{sub 2})(H{sub 2}O){sub 2}][(UO{sub 2})(VO{sub 4})]{sub 3{r_brace}}.H{sub 2}O (isoPrU4V3), (N(CH{sub 3}){sub 4}){l_brace}[(UO{sub 2})(H{sub 2}O){sub 2}][(UO{sub 2})(VO{sub 4})]{sub 3{r_brace}}.H{sub 2}O (TMetU4V3), (C{sub 6}NH{sub 14}){l_brace}[(UO{sub 2})(H{sub 2}O){sub 2}][(UO{sub 2})(VO{sub 4})]{sub 3{r_brace}}.H{sub 2}O (CHexU4V3), and (C{sub 4}NH{sub 12}){l_brace}[(UO{sub 2})(H{sub 2}O)][(UO{sub 2})(VO{sub 4})]{sub 3{r_brace}} (TButU4V3) were prepared from mild-hydrothermal reactions using dimethylamine, pyridine, isopropylamine, tetramethylammonium hydroxide, cyclohexylamine and tertiobutylamine, respectively, with uranyl nitrate and vanadium oxide in acidic medium. The structures were solved using single-crystal X-ray diffraction data. The compounds exhibit three-dimensional uranyl-vanadate inorganic frameworks built from uranophane-type uranyl-vanadate layers pillared by uranyl polyhedra with cavities in between occupied by protonated organic moieties. In the uranyl-vanadate layers the orientations of the vanadate tetrahedra give new geometrical isomers leading to unprecedented pillared systems and new inorganic frameworks with U/V=4/3. Crystallographic data: (DMetU5V4) orthorhombic, Cmc2{sub 1} space group, a=15.6276(4), b=14.1341(4), c=13.6040(4) A; (DMetU4V3) monoclinic, P2{sub 1}/n space group, a=10.2312(4), b=13.5661(7), c=17.5291(7) A, {beta}=96.966(2); (PyrU5V4), triclinic, P1 space group, a=9.6981(3), b=9.9966(2), c=10.5523(2) A, {alpha}=117.194(1), {beta}=113.551(1), {gamma}=92.216(1){sup o}; (isoPrU4V3) monoclinic, P2{sub 1}/n space group, a=10.3507(1), b=13.6500(2), c=17.3035(2) A, {beta}=97.551(1){sup o}; (TMetU4V3) orthorhombic, Pbca space group, a=17.1819(2), b=13.6931(1), c=21.4826(2) A; (CHexU4V3), triclinic P-1 space group, a=9.8273(6), b=11.0294(7), c=12.7506(8) A, {alpha}=98.461(3), {beta}=96.437(3), {gamma}=105.955(3){sup o}; (TButU4V3), monoclinic, P2{sub 1}/m space group, a=9.8048(4), b=17.4567(8), c=15.4820(6) A, {beta}=106.103(2). - Graphical abstract: The various type of PBP pillars P2, P3, P4, and P4' in the three-dimensional inorganic frameworks based on the uranophane-type sheet in monoamine templated uranyl-vanadates.

  11. Influence of uranyl speciation and iron oxides on uranium biogeochemical redox reactions

    SciTech Connect (OSTI)

    Stewart, B.D.; Amos, R.T.; Nico, P.S.; Fendorf, S.

    2010-03-15

    Uranium is a pollutant of concern to both human and ecosystem health. Uranium's redox state often dictates its partitioning between the aqueous- and solid-phases, and thus controls its dissolved concentration and, coupled with groundwater flow, its migration within the environment. In anaerobic environments, the more oxidized and mobile form of uranium (UO{sub 2}{sup 2+} and associated species) may be reduced, directly or indirectly, by microorganisms to U(IV) with subsequent precipitation of UO{sub 2}. However, various factors within soils and sediments may limit biological reduction of U(VI), inclusive of alterations in U(VI) speciation and competitive electron acceptors. Here we elucidate the impact of U(VI) speciation on the extent and rate of reduction with specific emphasis on speciation changes induced by dissolved Ca, and we examine the impact of Fe(III) (hydr)oxides (ferrihydrite, goethite and hematite) varying in free energies of formation on U reduction. The amount of uranium removed from solution during 100 h of incubation with S. putrefaciens was 77% with no Ca or ferrihydrite present but only 24% (with ferrihydrite) and 14% (no ferrihydrite) were removed for systems with 0.8 mM Ca. Imparting an important criterion on uranium reduction, goethite and hematite decrease the dissolved concentration of calcium through adsorption and thus tend to diminish the effect of calcium on uranium reduction. Dissimilatory reduction of Fe(III) and U(VI) can proceed through different enzyme pathways, even within a single organism, thus providing a potential second means by which Fe(III) bearing minerals may impact U(VI) reduction. We quantify rate coefficients for simultaneous dissimilatory reduction of Fe(III) and U(VI) in systems varying in Ca concentration (0 to 0.8 mM), and using a mathematical construct implemented with the reactive transport code MIN3P, we reveal the predominant influence of uranyl speciation, specifically the formation of uranyl-calcium-carbonato complexes, and ferrihydrite on the rate and extent of uranium reduction in complex geochemical systems.

  12. Experimental critical parameters of enriched uranium solution in annular tank geometries

    SciTech Connect (OSTI)

    Rothe, R.E.

    1996-04-01

    A total of 61 critical configurations are reported for experiments involving various combinations of annular tanks into which enriched uranium solution was pumped. These experiments were performed at two widely separated times in the 1980s under two programs at the Rocky Flats Plant`s Critical Mass Laboratory. The uranyl nitrate solution contained about 370 g of uranium per liter, but this concentration varied a little over the duration of the studies. The uranium was enriched to about 93% [sup 235]U. All tanks were typical of sizes commonly found in nuclear production plants. They were about 2 m tall and ranged in diameter from 0.6 m to 1.5 m. Annular thicknesses and conditions of neutron reflection, moderation, and absorption were such that criticality would be achieved with these dimensions. Only 13 of the entire set of 74 experiments proved to be subcritical when tanks were completely filled with solution. Single tanks of several radial thicknesses were studied as well as small line arrays (1 x 2 and 1 x 3) of annular tanks. Many systems were reflected on four sides and the bottom by concrete, but none were reflected from above. Many experiments also contained materials within and outside the annular regions that contained strong neutron absorbers. One program had such a thick external moderator/absorber combination that no reflector was used at all.

  13. Preparation of U.sub.3 O.sub.8

    DOE Patents [OSTI]

    Johnson, David R. (Aiken, SC)

    1980-01-01

    A method is described for the preparation of U.sub.3 O.sub.8 nuclear fuel material by direct precipitation of uranyl formate monohydrate from uranyl nitrate solution. The uranyl formate monohydrate precipitate is removed, dried and calcined to produce U.sub.3 O.sub.8 having a controlled particle size distribution.

  14. Use of tensiometer for in situ measurement of nitrate leaching

    SciTech Connect (OSTI)

    Li, K.; Reddy, M.R.

    1999-07-01

    In order to monitor nitrate leaching from non-point source pollution, this study used tensiometers to measure in situ nitrate concentration and soil-moisture potential. Instead of filling the tensiometers with pure water, the study filled the tensiometers with nitrate ionic strength adjuster (ISA, 1 M (NH{sub 4}){sub 2}SO{sub 4}). After the installation of the tensiometers at various depths along soil profiles, a portable pressure transducer was used to measure the soil moisture potential, and a nitrate electrode attached to an ion analyzer was used to measure the nitrate concentration in situ. The measurement was continuous and non-destructive. To test this method in the laboratory, eight bottles filled with pure sand were treated with known nitrate solutions, and a tensiometer was placed in each bottle. Measurements were taken every day for 30 days. Laboratory test showed a linear relationship between the known nitrate concentration and the tensiometer readings (R{sup 2} = 0.9990). Then a field test was conducted in a watermelon field with green manure mulch. Field data indicated a potential of nitrate leaching below the soil depth of 100 cm when crop uptake of nutrients was low.

  15. Diffusion and Adsorption of Uranyl Carbonate Species in Nanosized Mineral Fractures

    SciTech Connect (OSTI)

    Kerisit, Sebastien N.; Liu, Chongxuan

    2012-02-07

    Atomistic simulations were performed to study the diffusion and adsorption of Ca{sub 2}UO{sub 2}(CO{sub 3}){sub 3} and of some of its constituent species, i.e., UO{sub 2}{sup 2+}, CO{sub 3}{sup 2-}, and UO{sub 2}CO{sub 3}, in feldspar nano-sized fractures. Feldspar is important to uranium remediation efforts at the U.S. Department of Energy Hanford site as it has been found in recent studies to host contaminants within its intragrain fractures. In addition, uranyl carbonate species are known to dominate U(VI) speciation in conditions relevant to the Hanford site. Molecular dynamics (MD) simulations showed that the presence of the feldspar surface diminishes the diffusion coefficients of all the species considered in this work and that the diffusion coefficients do not reach their bulk aqueous solution values in the center of a 2.5 nm fracture. Moreover, the MD simulations showed that the rate of decrease in the diffusion coefficients with decreasing distance from the surface is greater for larger adsorbing species. Free energy profiles of the same species adsorbing on the feldspar surface revealed a large exothermic free energy of adsorption for UO{sub 2}{sup 2+} and UO{sub 2}CO{sub 3}, which are able to adsorb to the surface with their uranium atom directly bonded to a surface hydroxyl oxygen, whereas adsorption of CO{sub 3}{sup 2-} and Ca{sub 2}UO{sub 2}(CO{sub 3}){sub 3}, which attach to the surface via hydrogen bonding from a surface hydroxyl group to a carbonate oxygen, was calculated to be either only slightly exothermic or endothermic.

  16. Electrochemical reduction of nitrate in the presence of an amide

    DOE Patents [OSTI]

    Dziewinski, Jacek J. (Los Alamos, NM); Marczak, Stanislaw (Los Alamos, NM)

    2002-01-01

    The electrochemical reduction of nitrates in aqueous solutions thereof in the presence of amides to gaseous nitrogen (N.sub.2) is described. Generally, electrochemical reduction of NO.sub.3 proceeds stepwise, from NO.sub.3 to N.sub.2, and subsequently in several consecutive steps to ammonia (NH.sub.3) as a final product. Addition of at least one amide to the solution being electrolyzed suppresses ammonia generation, since suitable amides react with NO.sub.2 to generate N.sub.2. This permits nitrate reduction to gaseous nitrogen to proceed by electrolysis. Suitable amides include urea, sulfamic acid, formamide, and acetamide.

  17. Plutonium nitrate bottle counter manual

    SciTech Connect (OSTI)

    Menlove, H.O.; Adams, E.L.; Holbrooks, O.R.

    1984-03-01

    A neutron coincidence counter has been designed for plutonium nitrate assay in large storage bottles. This assay system can be used in the reprocessing plant or in the nitrate-to-oxide conversion facility. The system is based on the family of neutron detectors similar to the high-level neutron coincidence counter. This manual describes the system and gives performance and calibration parameters for typical applications. 4 references, 11 figures, 9 tables.

  18. The Complexes of Bisphosphonate and Magnetite Nanoparticles to Remove Uranyl Ions from Aqueous Phase

    SciTech Connect (OSTI)

    Wang, L.; Yang, Z.; Gao, J.; Xu, K.; Gu, H.; Xu, B.; Zhang, B.; Zhang, X.

    2007-03-20

    Using tetraethyl-3-amino-propane-1,1-bisphosphonate (BP) as the functional molecule, we functionalized Fe3O4 magnetic nanoparticles via dopamine (DA) linkage to create a system with an Fe3O4-DA-BP nanostructure, which possesses high specificity for removing uranyl ions from water or blood. This work demonstrates that magnetic nanoparticles, combined with specific receptor-ligand interactions, promise a sensitive and rapid platform for the detection, recovery, and decorporation of radioactive metal toxins from biological environment.

  19. SEPARATION OF RUTHENIUM FROM AQUEOUS SOLUTIONS

    DOE Patents [OSTI]

    Callis, C.F.; Moore, R.L.

    1959-09-01

    >The separation of ruthenium from aqueous solutions containing uranium plutonium, ruthenium, and fission products is described. The separation is accomplished by providing a nitric acid solution of plutonium, uranium, ruthenium, and fission products, oxidizing plutonium to the hexavalent state with sodium dichromate, contacting the solution with a water-immiscible organic solvent, such as hexone, to extract plutonyl, uranyl, ruthenium, and fission products, reducing with sodium ferrite the plutonyl in the solvent phase to trivalent plutonium, reextracting from the solvent phase the trivalent plutonium, ruthenium, and some fission products with an aqueous solution containing a salting out agent, introducing ozone into the aqueous acid solution to oxidize plutonium to the hexavalent state and ruthenium to ruthenium tetraoxide, and volatizing off the ruthenium tetraoxide.

  20. Combined uranous nitrate production consisting of undivided electrolytic cell and divided electrolytic cell (Electrolysis ? Electrolytic cell)

    SciTech Connect (OSTI)

    Yuan, Zhongwei; Yan, Taihong; Zheng, Weifang; Li, Xiaodong; Yang, Hui; Xian, Liang

    2013-07-01

    The electrochemical reduction of uranyl nitrate is a green, mild way to make uranous ions. Undivided electrolyzers whose maintenance is less but their conversion ratio and current efficiency are low, have been chosen. However, at the beginning of undivided electrolysis, high current efficiency can also be maintained. Divided electrolyzers' conversion ratio and current efficiency is much higher because the re-oxidation of uranous on anode is avoided, but their maintenance costs are more, because in radioactive environment the membrane has to be changed after several operations. In this paper, a combined method of uranous production is proposed which consists of 2 stages: undivided electrolysis (early stage) and divided electrolysis (late stage) to benefit from the advantages of both electrolysis modes. The performance of the combined method was tested. The results show that in combined mode, after 200 min long electrolysis (80 min undivided electrolysis and 120 min divided electrolysis), U(IV) yield can achieve 92.3% (500 ml feed, U 199 g/l, 72 cm{sup 2} cathode, 120 mA/cm{sup 2}). Compared with divided mode, about 1/3 working time in divided electrolyzer is reduced to achieve the same U(IV) yield. If 120 min long undivided electrolysis was taken, more than 1/2 working time can be reduced in divided electrolyzer, which means that about half of the maintenance cost can also be reduced. (authors)

  1. Development of an Immobilisation Technology for Radioactive Waste Solution from Mo-99 Production

    SciTech Connect (OSTI)

    Sizgek, G.D.; Sizgek, E.

    2006-07-01

    Australian Nuclear Science and Technology Organisation (ANSTO) developed a method to immobilize the Intermediate Level Liquid Waste (ILLW) arising from its Mo-99 production process. The immobilisation process involves impregnation of waste solution into ceramic precursor powders, drying, calcining and consolidation (Hot Isostatic Pressing, HIP) to produce final ceramic waste form. Ceramic precursor powder is produced by spray drying of a sol-gel based colloidal dispersion. These free-flowing, microspherical, 20-80 microns, precursors have porosity of 40-50%. An in-house custom designed and manufactured microwave-heated and mechanically fluidized mixer-drier was used for impregnation of the precursor powder with the simulated waste (Depleted Uranyl Nitrate Hexahydrate, DUNH, and inactive Cs, Sr nitrates as fission products) and drying. During impregnation an evaporation rate of 1 l/h water per kW microwave energy in steady state was achieved by matching the feed rate of DUNH to produce equivalent of 35% UO{sub 2} loading. It was demonstrated that the tuned microwave energy can be delivered to the mixer-drier during the entire impregnation process within very low reflection values. The samples of the waste loaded free-flowing powder were subsequently calcined at 750 deg. C under reducing atmosphere for thermal denitration and mineral phase nucleation. Calcined powders were filled into cans. After evacuation and sealing, the cans were isostatically pressed at 1260 deg. C. The consolidated ceramic waste form produced from the DUNH run has been assessed by durability and material characterization tests. Successful confirmation of each processing step at pilot and/or plant scale, has led to the design and construction of the overall process at full scale (equivalent of processing 8 kg U per batch) in a simulated hot-cell mock-up plant. The constructed plant mainly consists of a Microwave-heated Mechanical Fluidized Bed (MWMFB) mixer-drier a fluidized bed calciner, an off gas unit, material transfer/holding and can filling units. Performance of the overall process by integrating each of the processing steps and material transfer operations are currently being tested with inactive simulants from the point of remote operated plant design perspective. Definitive design of a hot-cell production system has been initiated in parallel to the mock-up plant tests. This paper describes the results of both full-scale DUNH impregnation run and inactive mock-up plant tests in developing unique Mo-99 waste immobilisation technology. (authors)

  2. Process for extracting technetium from alkaline solutions

    DOE Patents [OSTI]

    Moyer, Bruce A. (Oak Ridge, TN); Sachleben, Richard A. (Knoxville, TN); Bonnesen, Peter V. (Knoxville, TN)

    1995-01-01

    A process for extracting technetium values from an aqueous alkaline solution containing at least one alkali metal hydroxide and at least one alkali metal nitrate, the at least one alkali metal nitrate having a concentration of from about 0.1 to 6 molar. The solution is contacted with a solvent consisting of a crown ether in a diluent for a period of time sufficient to selectively extract the technetium values from the aqueous alkaline solution. The solvent containing the technetium values is separated from the aqueous alkaline solution and the technetium values are stripped from the solvent.

  3. Waste Isolation Pilot Plant Nitrate Salt Bearing Waste Container...

    Office of Environmental Management (EM)

    Nitrate Salt Bearing Waste Container Isolation Plan Waste Isolation Pilot Plant Nitrate Salt Bearing Waste Container Isolation Plan The purpose of this document is to provide the ...

  4. Sandia Energy - Molten Nitrate Salt Initial Flow Testing is a...

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

    Nitrate Salt Initial Flow Testing is a Tremendous Success Home Renewable Energy News Concentrating Solar Power Solar Molten Nitrate Salt Initial Flow Testing is a Tremendous...

  5. Synthesis of a new energetic nitrate ester

    SciTech Connect (OSTI)

    Chavez, David E

    2008-01-01

    Nitrate esters have been known as useful energetic materials since the discovery of nitroglycerin by Ascanio Sobrero in 1846. The development of methods to increase the safety and utility of nitroglycerin by Alfred Nobel led to the revolutionary improvement in the utility of nitroglycerin in explosive applications in the form of dynamite. Since then, many nitrate esters have been prepared and incorporated into military applications such as double-based propellants, detonators and as energetic plasticizers. Nitrate esters have also been shown to have vasodilatory effects in humans and thus have been studied and used for treatments of ailments such as angina. The mechanism of the biological response towards nitrate esters has been elucidated recently. Interestingly, many of the nitrate esters used for military purposes are liquids (ethylene glycol dinitrate, propylene glycol dinitrate, etc). Pentaerythritol tetranitrate (PETN) is one of the only solid nitrate esters, besides nitrocellulose, that is used in any application. Unfortunately, PETN melting point is above 100 {sup o}C, and thus must be pressed as a solid for detonator applications. A more practical material would be a melt-castable explosive, for potential simplification of manufacturing processes. Herein we describe the synthesis of a new energetic nitrate ester (1) that is a solid at ambient temperatures, has a melting point of 85-86 {sup o}C and has the highest density of any known nitrate ester composed only of carbon, hydrogen, nitrogen and oxygen. We also describe the chemical, thermal and sensitivity properties of 1 as well as some preliminary explosive performance data.

  6. Remediated Nitrate Salt Drums Safety Update | Department of Energy

    Office of Environmental Management (EM)

    Remediated Nitrate Salt Drums Safety Update Remediated Nitrate Salt Drums Safety Update Topic: Mr. Nickless, Environmental Management Los Alamos, Provided a presentation on the status of the Nitrate Salt waste at Los Alamos. More Documents & Publications Los Alamos National Laboratory TRU Waste Update Los Alamos National Laboratory Accident Investigation Board Corrective Action Plan Update Treatment of Remediated Nitrate Salts

  7. Process for the preparation of an energetic nitrate ester

    DOE Patents [OSTI]

    Chavez, David E; Naud, Darren L; Hiskey, Michael A

    2013-12-17

    A process for the preparation of an energetic nitrate ester compound and related intermediates is provided.

  8. Cesium recovery from aqueous solutions

    DOE Patents [OSTI]

    Goodhall, C. A.

    1960-09-13

    A process for recovering cesium from aqueous solutions is given in which precipitation on zinc ferricyanide is used. The precipitation is preferably carried out in solutions containing at least 0.0004M zinc ferricyanide, an acidity ranging from 0.2N mineral acid to 0.61N acid deficiency, and 1 to 2.5M aluminum nitrate. (D.L.C.)

  9. Scale-Dependent Rates of Uranyl Surface Complexation Reaction in Sediments

    SciTech Connect (OSTI)

    Liu, Chongxuan; Shang, Jianying; Kerisit, Sebastien N.; Zachara, John M.; Zhu, Weihuang

    2013-03-15

    Scale-dependency of uranyl[U(VI)] surface complexation rates was investigated in stirred flow-cell and column systems using a U(VI)-contaminated sediment from the US Department of Energy, Hanford site, WA. The experimental results were used to estimate the apparent rate of U(VI) surface complexation at the grain-scale and in porous media. Numerical simulations using molecular, pore-scale, and continuum models were performed to provide insights into and to estimate the rate constants of U(VI) surface complexation at the different scales. The results showed that the grain-scale rate constant of U(VI) surface complexation was over 3 to 10 orders of magnitude smaller, dependent on the temporal scale, than the rate constant calculated using the molecular simulations. The grain-scale rate was faster initially and slower with time, showing the temporal scale-dependency. The largest rate constant at the grain-scale decreased additional 2 orders of magnitude when the rate was scaled to the porous media in the column. The scaling effect from the grain-scale to the porous media became less important for the slower sorption sites. Pore-scale simulations revealed the importance of coupled mass transport and reactions in both intragranular and inter-granular domains, which caused both spatial and temporal dependence of U(VI) surface complexation rates in the sediment. Pore-scale simulations also revealed a new rate-limiting mechanism in the intragranular porous domains that the rate of coupled diffusion and surface complexation reaction was slower than either process alone. The results provided important implications for developing models to scale geochemical/biogeochemical reactions.

  10. Submergible torch for treating waste solutions and method thereof

    DOE Patents [OSTI]

    Mattus, A.J.

    1994-12-06

    A submergible torch is described for removing nitrate and/or nitrite ions from a waste solution containing nitrate and/or nitrite ions comprises: a torch tip, a fuel delivery mechanism, a fuel flow control mechanism, a catalyst, and a combustion chamber. The submergible torch is ignited to form a flame within the combustion chamber of the submergible torch. The torch is submerged in a waste solution containing nitrate and/or nitrite ions in such a manner that the flame is in contact with the waste solution and the catalyst and is maintained submerged for a period of time sufficient to decompose the nitrate and/or nitrite ions present in the waste solution. 2 figures.

  11. Submergible torch for treating waste solutions and method thereof

    DOE Patents [OSTI]

    Mattus, Alfred J. (Oak Ridge, TN)

    1994-01-01

    A submergible torch for removing nitrate and/or nitrite ions from a waste solution containing nitrate and/or nitrite ions comprises: a torch tip, a fuel delivery mechanism, a fuel flow control mechanism, a catalyst, and a combustion chamber. The submergible torch is ignited to form a flame within the combustion chamber of the submergible torch. The torch is submerged in a waste solution containing nitrate and/or nitrite ions in such a manner that the flame is in contact with the waste solution and the catalyst and is maintained submerged for a period of time sufficient to decompose the nitrate and/or nitrite ions present in the waste solution.

  12. Submergible torch for treating waste solutions and method thereof

    DOE Patents [OSTI]

    Mattus, Alfred J. (Oak Ridge, TN)

    1995-01-01

    A submergible torch for removing nitrate and/or nitrite ions from a waste solution containing nitrate and/or nitrite ions comprises: a torch tip, a fuel delivery mechanism, a fuel flow control mechanism, a catalyst, and a combustion chamber. The submergible torch is ignited to form a flame within the combustion chamber of the submergible torch. The torch is submerged in a waste solution containing nitrate and/or nitrite ions in such a manner that the flame is in contact with the waste solution and the catalyst and is maintained submerged for a period of time sufficient to decompose the nitrate and/or nitrite ions present in the waste solution.

  13. Nitrate Salt Surrogate Blending Scoping Test Plan

    SciTech Connect (OSTI)

    Anast, Kurt Roy

    2015-11-13

    Test blending equipment identified in the “Engineering Options Assessment Report: Nitrate Salt Waste Stream Processing”. Determine if the equipment will provide adequate mixing of zeolite and surrogate salt/Swheat stream; optimize equipment type and operational sequencing; impact of baffles and inserts on mixing performance; and means of validating mixing performance

  14. Denitration of High Nitrate Salts Using Reductants

    SciTech Connect (OSTI)

    HD Smith; EO Jones; AJ Schmidt; AH Zacher; MD Brown; MR Elmore; SR Gano

    1999-05-03

    This report describes work conducted by Pacific Northwest National Laboratory (PNNL), in conjunction with Idaho National Engineering and Environmental Laboratory (INEEL), to remove nitrates in simulated low-activity waste (LAW). The major objective of this work was to provide data for identifying and demonstrating a technically viable and cost-effective approach to condition LAW for immobilization (grout).

  15. NITRATE DESTRUCTION LITERATURE SURVEY AND EVALUATION CRITERIA

    SciTech Connect (OSTI)

    Steimke, J.

    2011-02-01

    This report satisfies the initial phase of Task WP-2.3.4 Alternative Sodium Recovery Technology, Subtask 1; Develop Near-Tank Nitrate/Nitrite Destruction Technology. Some of the more common anions in carbon steel waste tanks at SRS and Hanford Site are nitrate which is corrosive, and nitrite and hydroxide which are corrosion inhibitors. At present it is necessary to periodically add large quantities of 50 wt% caustic to waste tanks. There are three primary reasons for this addition. First, when the contents of salt tanks are dissolved, sodium hydroxide preferentially dissolves and is removed. During the dissolution process the concentration of free hydroxide in the tank liquid can decrease from 9 M to less than 0.2 M. As a result, roughly half way through the dissolution process large quantities of sodium hydroxide must be added to the tank to comply with requirements for corrosion control. Second, hydroxide is continuously consumed by reaction with carbon dioxide which occurs naturally in purge air used to prevent buildup of hydrogen gas inside the tanks. The hydrogen is generated by radiolysis of water. Third, increasing the concentration of hydroxide increases solubility of some aluminum compounds, which is desirable in processing waste. A process that converts nitrate and nitrite to hydroxide would reduce certain costs. (1) Less caustic would be purchased. (2) Some of the aluminum solid compounds in the waste tanks would become more soluble so less mass of solids would be sent to High Level Vitrification and therefore it would be not be necessary to make as much expensive high level vitrified product. (3) Less mass of sodium would be fed to Saltstone at SRS or Low Level Vitrification at Hanford Site so it would not be necessary to make as much low level product. (4) At SRS less nitrite and nitrate would be sent to Defense Waste Processing Facility (DWPF) so less formic acid would be consumed there and less hydrogen gas would be generated. This task involves literature survey of technologies to perform the nitrate to hydroxide conversion, selection of the most promising technologies, preparation of a flowsheet and design of a system. The most promising technologies are electrochemical reduction of nitrates and chemical reduction with hydrogen or ammonia. The primary reviewed technologies are listed and they aredescribed in more detail later in the report: (1) Electrochemical destruction; (2) Chemical reduction with agents such as ammonia, hydrazine or hydrogen; (3) Hydrothermal reduction process; and (4) Calcination. Only three of the technologies on the list have been demonstrated to generate usable amounts of caustic; electrochemical reduction and chemical reduction with ammonia, hydrazine or hydrogen and hydrothermal reduction. Chemical reduction with an organic reactant such as formic acid generates carbon dioxide which reacts with caustic and is thus counterproductive. Treatment of nitrate with aluminum or other active metals generates a solid product. High temperature calcination has the potential to generate sodium oxide which may be hydrated to sodium hydroxide, but this is unproven. The following criteria were developed to evaluate the most suitable option. The numbers in brackets after the criteria are relative weighting factors to account for importance: (1) Personnel exposure to radiation for installation, routine operation and maintenance; (2) Non-radioactive safety issues; (3) Whether the technology generates caustic and how many moles of caustic are generated per mole of nitrate plus nitrite decomposed; (4) Whether the technology can handle nitrate and nitrite at the concentrations encountered in waste; (5) Maturity of technology; (6) Estimated annual cost of operation (labor, depreciation, materials, utilities); (7) Capital cost; (8) Selectivity to nitrogen as decomposition product (other products are flammable and/or toxic); (9) Impact of introduced species; (10) Selectivity for destruction of nitrate vs. nitrite; and (11) Cost of deactivation and demolition. Each technology was given a score from one

  16. Treatment of Remediated Nitrate Salts | Department of Energy

    Energy Savers [EERE]

    Treatment of Remediated Nitrate Salts Treatment of Remediated Nitrate Salts Topic: Plan for remediation the nitrate salt waste from the 3706 campaign that is currently stored at Material Disposal Area G, presenter was David Funk, LANS. PDF icon Nitrate Salts - November 18, 2015 More Documents & Publications Accident Investigation Report Phase II Accident Investigation Report - Radiological Release Amount of Zeolite Required to Meet the Constraints Established by the Energetic Materials

  17. Supplemental Cooling for Nitrate Salt Waste

    SciTech Connect (OSTI)

    Goldberg, Mitchell S.

    2015-08-19

    In July 2015, Los Alamos National Laboratory completed installation of a supplemental cooling system in the structure where remediated nitrate salt waste drums are stored. Although the waste currently is in a safe configuration and is monitored daily,controlling the temperature inside the structure adds another layer of protection for workers, the public,and the environment.This effort is among several layers of precautions designed to secure the waste.

  18. Project Profile: Advanced Nitrate Salt Central Receiver Power Plant |

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

    Department of Energy Nitrate Salt Central Receiver Power Plant Project Profile: Advanced Nitrate Salt Central Receiver Power Plant Abengoa logo Abengoa, under the Baseload CSP FOA, will demonstrate a 100-megawatt electrical (MWe) central receiver plant using nitrate salt as the receiver coolant, thermal storage medium, and heat transport fluid in the steam generator. Approach Photo of two lit towers surrounded by much smaller blue flat plates that are mounted on the ground. The plan is to

  19. Electrochemical cell having an alkali-metal-nitrate electrode

    DOE Patents [OSTI]

    Roche, M.F.; Preto, S.K.

    1982-06-04

    A power-producing secondary electrochemical cell includes a molten alkali metal as the negative-electrode material and a molten-nitrate salt as the positive-electrode material. The molten material in the respective electrodes are separated by a solid barrier of alkali-metal-ion conducting material. A typical cell includes active materials of molten sodium separated from molten sodium nitrate and other nitrates in mixture by a layer of sodium ..beta..'' alumina.

  20. Waste Isolation Pilot Plant Nitrate Salt Bearing Waste Container

    Office of Environmental Management (EM)

    Nitrate Salt Bearing Waste Container Isolation Plan Prepared in Response to New Mexico ... (DOE) and Nuclear Waste Partnership LLC (NWP), collectively referred to as the Permittees. ...

  1. Molten Nitrate Salt Development for Thermal Energy Storage in...

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

    MOLTEN NITRATE SALT DEVELOPMENT FOR THERMAL ENERGY STORAGE IN PARABOLIC TROUGH SOLAR POWER SYSTEMS Robert W. Bradshaw and Nathan P. Siegel Sandia National Laboratories, PO Box 969 ...

  2. Operating Experience Level 2, Evaluation of Nitrate Bearing Transurani...

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

    015 OE-2 2015-01: Evaluation of Nitrate Bearing Transuranic Waste Streams This Operating Experience Level 2 (OE-2) document provides actions to perform an evaluation of...

  3. Corrosion of aluminides by molten nitrate salt

    SciTech Connect (OSTI)

    Tortorelli, P.F.; Bishop, P.S.

    1990-01-01

    The corrosion of titanium-, iron-, and nickel-based aluminides by a highly aggressive, oxidizing NaNO{sub 3}(-KNO{sub 3})-Na{sub 2}O{sub 2} has been studied at 650{degree}C. It was shown that weight changes could be used to effectively evaluate corrosion behavior in the subject nitrate salt environments provided these data were combined with salt analyses and microstructural examinations. The studies indicated that the corrosion of relatively resistant aluminides by these nitrate salts proceeded by oxidation and a slow release from an aluminum-rich product layer into the salt at rates lower than that associated with many other types of metallic materials. The overall corrosion process and resulting rate depended on the particular aluminide being exposed. In order to minimize corrosion of nickel or iron aluminides, it was necessary to have aluminum concentrations in excess of 30 at. %. However, even at a concentration of 50 at. % Al, the corrosion resistance of TiAl was inferior to that of Ni{sub 3}Al and Fe{sub 3}Al. At higher aluminum concentrations, iron, nickel, and iron-nickel aluminides exhibited quite similar weight changes, indicative of the principal role of aluminum in controlling the corrosion process in NaNO{sub 3}(-KNO{sub 3})-Na{sub 2}O{sub 2} salts. 20 refs., 5 figs., 3 tabs.

  4. Plant-Scale Concentration Column Designs for SHINE Target Solution Utilizing AG 1 Anion Exchange Resin

    SciTech Connect (OSTI)

    Stepinski, Dominique C.; Vandegrift, G. F.

    2015-09-30

    Argonne is assisting SHINE Medical Technologies (SHINE) in their efforts to develop SHINE, an accelerator-driven process that will utilize a uranyl-sulfate solution for the production of fission product Mo-99. An integral part of the process is the development of a column for the separation and recovery of Mo-99, followed by a concentration column to reduce the product volume from 15-25 L to <1 L. Argonne has collected data from batch studies and breakthrough column experiments to utilize the VERSE (Versatile Reaction Separation) simulation program (Purdue University) to design plant-scale product recovery and concentration processes.

  5. Method for producing microcomposite powders using a soap solution

    DOE Patents [OSTI]

    Maginnis, Michael A. (Coker, AL); Robinson, David A. (Mobile, AL)

    1996-01-01

    A method for producing microcomposite powders for use in superconducting and non-superconducting applications. A particular method to produce microcomposite powders for use in superconducting applications includes the steps of: (a) preparing a solution including ammonium soap; (b) dissolving a preselected amount of a soluble metallic such as silver nitrate in the solution including ammonium soap to form a first solution; (c) adding a primary phase material such as a single phase YBC superconducting material in particle form to the first solution; (d) preparing a second solution formed from a mixture of a weak acid and an alkyl-mono-ether; (e) adding the second solution to the first solution to form a resultant mixture; (f) allowing the resultant mixture to set until the resultant mixture begins to cloud and thicken into a gel precipitating around individual particles of the primary phase material; (g) thereafter drying the resultant mixture to form a YBC superconducting material/silver nitrate precursor powder; and (h) calcining the YBC superconducting material/silver nitrate precursor powder to convert the silver nitrate to silver and thereby form a YBC/silver microcomposite powder wherein the silver is substantially uniformly dispersed in the matrix of the YBC material.

  6. Enhanced liquid-liquid anion exchange using macrocyclic anion receptors: effect of receptor structure on sulphate-nitrate exchange selectivity

    SciTech Connect (OSTI)

    Moyer, Bruce A; Sloop Jr, Frederick {Fred} V; Fowler, Christopher J; Haverlock, Tamara; Kang, Hyun Ah; Delmau, Laetitia Helene; Bau, Diadra; Hossain, Alamgir; Bowman-James, Kristin; Shriver, James A.; Gross, Mr. Dustin E.; Bill, Nathan; Marquez, Manuel; Lynch, Vincent M.; Sessler, Jonathan L.

    2010-01-01

    When certain macrocyclic anion receptors are added to a chloroform solution of the nitrate form of a lipophilic quaternary ammonium salt (methyltri-C8,10-ammonium nitrate, Aliquat 336N), the extraction of sulphate from an aqueous sodium nitrate solution via exchange with the organic-phase nitrate is significantly enhanced. Eight macrocycles were surveyed, including two derivatives of a tetraamide macrocycle, five derivatives of calix[4]pyrrole and -decafluorocalix[5]pyrrole. Under the hypothesis that the enhancement originates from sulphate binding by the anion receptors in the chloroform phase, it was possible to obtain reasonable fits to the sulphate distribution survey data based on the formation of 1:1 and 2:1 receptor:sulphate complexes in the chloroform phase. Apparent 1:1 sulphate-binding constants obtained from the model in this system fell in the range . Comparison of the results for the various anion receptors included in this study reveals that sulphate binding is sensitive to the nature of the substituents on the parent macrocycle scaffolds in a way that does not follow straightforwardly from simple chemical expectations, such as electron-withdrawing effects on hydrogen-bond donor strength.

  7. Effect of Phosphate, Fluoride, and Nitrate on Gibbsite Dissolution Rate and Solubility

    SciTech Connect (OSTI)

    Herting, Daniel L.

    2014-01-29

    Laboratory tests have been completed with simulated tank waste samples to investigate the effects of phosphate, fluoride, and nitrate on the dissolution rate and equilibrium solubility of gibbsite in sodium hydroxide solution at 22 and 40{degrees}C. Results are compared to relevant literature data and to computer model predictions. The presence of sodium nitrate (3 M) caused a reduction in the rate of gibbsite dissolution in NaOH, but a modest increase in the equilibrium solubility of aluminum. The increase in solubility was not as large, though, as the increase predicted by the computer model. The presence of phosphate, either as sodium phosphate or sodium fluoride phosphate, had a negligible effect on the rate of gibbsite dissolution, but caused a slight increase in aluminum solubility. The magnitude of the increased solubility, relative to the increase caused by sodium nitrate, suggests that the increase is due to ionic strength (or water activity) effects, rather than being associated with the specific ion involved. The computer model predicted that phosphate would cause a slight decrease in aluminum solubility, suggesting some Al-PO4 interaction. No evidence was found of such an interaction.

  8. Preparation of thin ceramic films via an aqueous solution route

    DOE Patents [OSTI]

    Pederson, Larry R. (Kennewick, WA); Chick, Lawrence A. (Richland, WA); Exarhos, Gregory J. (Richland, WA)

    1989-01-01

    A new chemical method of forming thin ceramic films has been developed. An aqueous solution of metal nitrates or other soluble metal salts and a low molecular weight amino acid is coated onto a substrate and pyrolyzed. The amino acid serves to prevent precipitation of individual solution components, forming a very viscous, glass-like material as excess water is evaporated. Using metal nitrates and glycine, the method has been demonstrated for zirconia with various levels of yttria stabilization, for lanthanum-strontium chromites, and for yttrium-barium-copper oxide superconductors on various substrates.

  9. Decontamination of water using nitrate selective ion exchange resin

    DOE Patents [OSTI]

    Lockridge, J.E.; Fritz, J.S.

    1990-07-31

    A method for nitrate decontamination of water which involves passing the water through a bed of alkyl phosphonium anion exchange resin which has pendant alkyl groups of C[sub 3] or larger.

  10. Decontamination of water using nitrate selective ion exchange resin

    DOE Patents [OSTI]

    Lockridge, James E. (Ames, IA); Fritz, James S. (Ames, IA)

    1990-07-31

    A method for nitrate decontamination of water which involves passing the water through a bed of alkyl phosphonium anion exchange resin which has pendant alkyl groups of C.sub.3 or larger.

  11. Evaluation of Nitrate-Bearing Transuranic Waste Streams

    Energy Savers [EERE]

    OE-2: 2015-1 June 2015 Evaluation of Nitrate-Bearing Transuranic Waste Streams PURPOSE This Operating Experience Level 2 (OE-2) document provides actions to perform an evaluation...

  12. Molecular recognition of nitrated fatty acids by PPAR[gamma

    SciTech Connect (OSTI)

    Li, Yong; Zhang, Jifeng; Schopfer, Francisco J.; Martynowski, Dariusz; Garcia-Barrio, Minerva T.; Kovach, Amanda; Suino-Powell, Kelly; Baker, Paul R.S.; Freeman, Bruce A.; Chen, Y. Eugene; Xu, H. Eric

    2010-03-08

    Peroxisome proliferator activated receptor-{gamma} (PPAR{gamma}) regulates metabolic homeostasis and adipocyte differentiation, and it is activated by oxidized and nitrated fatty acids. Here we report the crystal structure of the PPAR{gamma} ligand binding domain bound to nitrated linoleic acid, a potent endogenous ligand of PPAR{gamma}. Structural and functional studies of receptor-ligand interactions reveal the molecular basis of PPAR{gamma} discrimination of various naturally occurring fatty acid derivatives.

  13. Nitrate Salt Bearing Transuranic Waste Container Monitoring | Department of

    Office of Environmental Management (EM)

    Energy Nitrate Salt Bearing Transuranic Waste Container Monitoring Nitrate Salt Bearing Transuranic Waste Container Monitoring This document was used to determine facts and conditions during the Department of Energy Accident Investigation Board's investigation into the radiological release event at the Waste Isolation Pilot Plant. Additional documents referenced and listed in the Phase 2 Radiological Release Event at the Waste Isolation Pilot Plant on February 14, 2014, report in Attachment

  14. Nonaqueous purification of mixed nitrate heat transfer media

    DOE Patents [OSTI]

    Fiorucci, Louis C.; Morgan, Michael J.

    1983-12-20

    A nonaqueous, in-line method for removing carbonate and hydroxide contamination from a molten mixed sodium nitrate/potassium nitrate heat transfer salt. The method comprises dissolving a stoichiometric quantity of anhydrous Ca(NO.sub.3).sub.2 in the melt whereby an insoluble CaCO.sub.3 and Ca(OH).sub.2 precipitate is formed. The precipitate can be removed by settling, filtration or floatation techniques.

  15. Waste Isolation Pilot Plant Nitrate Salt Bearing Waste Container Isolation

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

    Plan | Department of Energy The purpose of this document is to provide the Plan required by the New Mexico Environment Department Administrative Order 05-20001 issued on May 20, 2014 to the U. S. Department of Energy and Nuclear Waste Partnership LLC. The Order, at paragraph 22, requires the Permittees to submit a WIPP Nitrate Salt Bearing Waste Container Isolation Plan for identified nitrate salt bearing waste disposed in the Waste Isolation Pilot Plant underground disposal facility. PDF

  16. Evaporation of iodine-containing off-gas scrubber solution

    DOE Patents [OSTI]

    Partridge, J.A.; Bosuego, G.P.

    1980-07-14

    Mercuric nitrate-nitric acid scrub solutions containing radioiodine may be reduced in volume without excessive loss of volatile iodine. The use of concentrated nitric acid during an evaporation process oxidizes the mercury-iodide complex to a less volatile mercuric iodate precipitate.

  17. Analytical Characterization of the Thorium Nitrate Stockpile

    SciTech Connect (OSTI)

    Mattus, CH

    2003-12-30

    For several years, Oak Ridge National Laboratory (ORNL) has been supporting the Defense Logistics Agency-Defense National Stockpile Center with stewardship of a thorium nitrate (ThN) stockpile. The effort for fiscal year 2002 was to prepare a sampling and analysis plan and to use the activities developed in the plan to characterize the ThN stockpile. The sampling was performed in June and July 2002 by RWE NUKEM with oversight by ORNL personnel. The analysis was performed by Southwest Research Institute of San Antonio, Texas, and data validation was performed by NFT, Inc., of Oak Ridge, Tennessee. Of the {approx} 21,000 drums in the stockpile, 99 were sampled and 53 were analyzed for total metals composition, radiological constituents (using alpha and gamma spectrometry), and oxidizing characteristics. Each lot at the Curtis Bay Depot was sampled. Several of the samples were also analyzed for density. The average density of the domestic ThN was found to be 1.89 {+-} 0.08 g/cm{sup 3}. The oxidizer test was performed following procedures issued by the United Nations in 1999. Test results indicated that none of the samples tested was a Division 5.1 oxidizer per Department of Transportation definition. The samples were analyzed for total metals following the U.S. Environmental Protection Agency methods SW-846-6010B and 6020 (EPA 2003) using a combination of inductively coupled plasma--atomic emission spectroscopy and inductively coupled plasma--mass spectroscopy techniques. The results were used to compare the composition of the eight Resource Conservation and Recovery Act metals present in the sample (arsenic, barium, cadmium, chromium, lead, mercury, selenium, and silver) to regulatory limits. None of the samples was found to be hazardous for toxicity characteristics. The radiological analyses confirmed, when possible, the results obtained by the inductively coupled plasma analyses. These results--combined with the historical process knowledge acquired on the material and the results of previous tests--classified the ThN as low-level radioactive waste for disposal purposes. This characterization was necessary to continue the efforts associated with disposition of the material at the Nevada Test Site, Mercury, Nevada. With the current work presented in this report, the analytical characterization phase is completed for this source material stockpile.

  18. Effect of Co-solutes on the Products and Solubility of Uranium(VI) Precipitated with Phosphate

    SciTech Connect (OSTI)

    Mehta, Vrajesh; Maillot, Fabien; Wang, Zheming; Catalano, Jeffrey G.; Giammar, Daniel E.

    2014-01-22

    Uranyl phosphate solids are often found with uranium ores, and their low solubility makes them promising target phases for in situ remediation of uranium-contaminated subsurface environments. The products and solubility of uranium(VI) precipitated with phosphate can be affected by the pH, dissolved inorganic carbon (DIC) concentration, and co-solute composition (e.g. Na+/Ca2+) of the groundwater. Batch experiments were performed to study the effect of these parameters on the products and extent of uranium precipitation induced by phosphate addition. In the absence of co-solute cations, chernikovite [H3O(UO2)(PO4)3H2O] precipitated despite uranyl orthophosphate [(UO2)3(PO4)24H2O] being thermodynamically more favorable under certain conditions. As determined using X-ray diffraction, electron microscopy, and laser induced fluorescence spectroscopy, the presence of Na+ or Ca2+ as a co-solute led to the precipitation of sodium autunite ([Na2(UO2)2(PO4)2] and autunite [Ca(UO2)2(PO4)2]), which are structurally similar to chernikovite. In the presence of sodium, the dissolved U(VI) concentrations were generally in agreement with equilibrium predictions of sodium autunite solubility. However, in the calcium-containing systems, the observed concentrations were below the predicted solubility of autunite, suggesting the possibility of uranium adsorption to or incorporation in a calcium phosphate precipitate in addition to the precipitation of autunite.

  19. Infrared Multiphoton Dissociation Spectroscopy of a Gas-Phase Complex of Uranyl and 3-Oxa-Glutaramide: An Extreme Red-Shift of the [O=U=O]? Asymmetric Stretch

    SciTech Connect (OSTI)

    Gibson, John K.; Hu, Hanshi; Van Stipdonk, Michael J.; Berden, Giel; Oomens, Jos; Li, Jun

    2015-04-09

    The gas-phase complex UO?(TMOGA)?? (TMOGA = tetramethyl-3-oxa-glutaramide) prepared by electrospray ionization was characterized by infrared multiphoton dissociation (IRMPD) spectroscopy. The IRMPD spectrum from 7001800 cm? was interpreted using a computational study based on density functional theory. The predicted vibrational frequencies are in good agreement with the measured values, with an average deviation of only 8 cm? (<1%) and a maximum deviation of 21 cm? (<2%). The only IR peak assigned to the linear uranyl moiety was the asymmetric ?? mode, which appeared at 965 cm? and was predicted by DFT as 953 cm?. This ?? frequency is red-shifted relative to bare uranyl, UO??, by ca. 150 cm? due to electron donation from the TMOGA ligands. Based on the degree of red-shifting, it is inferred that two TMOGA oxygen-donor ligands have a greater effective gas basicity than the four monodentate acetone ligands in UO?(acetone)??. The uranyl ?? frequency was also computed for uranyl coordinated by two TMGA ligands, in which the central Oether of TMOGA has been replaced by CH?. The computed ?? for UO?(TMGA)??, 950 cm?, is essentially the same as that for UO?(TMOGA)??, suggesting that electron donation to uranyl from the Oether of TMOGA is minor. The computed ?? asymmetric stretching frequencies for the three actinyl complexes, UO?(TMOGA)??, NpO?(TMOGA)?? and PuO?(TMOGA)??, are comparable. This similarity is discussed in the context of the relationship between ?? and intrinsic actinide-oxygen bond energies in actinyl complexes.

  20. Structure and dynamics of complexes of the uranyl ion with nonamethylimidodiphosphoramide (NIPA). 2. NMR studies of complexes (UO/sub 2/(NIPA)/sub 2/X)(CIO/sub 4/)/sub 2/ with X = H/sub 2/O, MeOH, EtOH, or Me/sub 2/CO

    SciTech Connect (OSTI)

    Rodehueser, L.; Rubini, P.R.; Bokolo, K.; Delpuech, J.J.

    1982-03-01

    The /sup 31/P and /sup 1/H spectra at -90/sup 0/C of the title uranyl complex ions (prepared as solutions of the solid perchlorates in inert anhydrous organic solvents (CH/sub 3/NO/sub 2/, CH/sub 2/Cl/sub 2/)) reveal a pentacoordinated arrangement of two symmetrically doubly bonded NIPA molecules and one solvent molecule about the uranyl group. In the case of (UO/sub 2/(NIPA)/sub 2/(EtOH))(ClO/sub 4/)/sub 2/, an intermolecular exchange between bound and free ethanol molecules is observed above -75/sup 0/C upon addition of ethanol to a solution of the complex. The observed rate law, k/sub inter/ = kK(EtOH)/(1 + K(EtOH) is accounted for by the existence of an outer-sphere complex (UO/sub 2//sup 2 +/(NIPA)/sub 2/(EtOH))EtOH in fast equilibrium (K) with the initial complex and free ethanol. The rate-determining step (k) consists of an outer-sphere to inner-sphere interchange of ethanol molecules. The thermodynamic and kinetic parameters are K(25/sup 0/C) = 15.8 dm/sup 3/ mol/sup -1/, k(25/sup 0/C) = 1.0 x 10/sup 4/s/sup -1/, ..delta..H and ..delta..H/sub inter//sup + +/ = -4.8 and 7.6 kcal mol/sup -1/, and ..delta..S and ..delta..S/sub inter//sup + +/ = 10.7 and -14.7 eu. A second exchange takes place at higher temperatures (above -30/sup 0/C) yielding full dynamic equivalence of the phosphorus nuclei of the coordinated NIPA molecules. The observed rate law k/sub intra/ = k/sub ex/(1 + K(EtOH)) reveals that the internal rearrangement of NIPA molecules occurs on the complex ion (UO/sub 2/(NIPA)/sub 2/(EtOH))/sup 2 +/ but not on the outer-sphere complex: k/sub ex/(25/sup 0/C) = 0.91 x 10/sup 3/s/sup -1/, ..delta..H/sub intra//sup + +/ = 10.6 kcal mol/sup -1/ and ..delta..S/sub intra//sup + +/ = -9.4 eu. Possible mechanisms for this exchange are discussed. 5 figures, 2 tables.

  1. Method for recovering palladium and technetium values from nuclear fuel reprocessing waste solutions

    DOE Patents [OSTI]

    Horwitz, E. Philip; Delphin, Walter H.

    1979-07-24

    A method for recovering palladium and technetium values from nuclear fuel reprocessing waste solutions containing these and other values by contacting the waste solution with an extractant of tricaprylmethylammonium nitrate in an inert hydrocarbon diluent which extracts the palladium and technetium values from the waste solution. The palladium and technetium values are recovered from the extractant and from any other coextracted values with a strong nitric acid strip solution.

  2. Speciation model selection by Monte Carlo analysis of optical absorption spectra: Plutonium(IV) nitrate complexes

    SciTech Connect (OSTI)

    Berg, John M.; Veirs, D. Kirk; Vaughn, Randolph B.; Cisneros, Michael R.; Smith, Coleman A.

    2000-06-01

    Standard modeling approaches can produce the most likely values of the formation constants of metal-ligand complexes if a particular set of species containing the metal ion is known or assumed to exist in solution equilibrium with complexing ligands. Identifying the most likely set of species when more than one set is plausible is a more difficult problem to address quantitatively. A Monte Carlo method of data analysis is described that measures the relative abilities of different speciation models to fit optical spectra of open-shell actinide ions. The best model(s) can be identified from among a larger group of models initially judged to be plausible. The method is demonstrated by analyzing the absorption spectra of aqueous Pu(IV) titrated with nitrate ion at constant 2 molal ionic strength in aqueous perchloric acid. The best speciation model supported by the data is shown to include three Pu(IV) species with nitrate coordination numbers 0, 1, and 2. Formation constants are {beta}{sub 1}=3.2{+-}0.5 and {beta}{sub 2}=11.2{+-}1.2, where the uncertainties are 95% confidence limits estimated by propagating raw data uncertainties using Monte Carlo methods. Principal component analysis independently indicates three Pu(IV) complexes in equilibrium. (c) 2000 Society for Applied Spectroscopy.

  3. Technical Area (TA)-54 Area G Nitrate-Salt Waste Container Response...

    Office of Environmental Management (EM)

    Technical Area (TA)-54 Area G Nitrate-Salt Waste Container Response Instructions Technical Area (TA)-54 Area G Nitrate-Salt Waste Container Response Instructions This document was...

  4. Polymer solutions

    DOE Patents [OSTI]

    Krawczyk, Gerhard Erich (Bremen, DE); Miller, Kevin Michael (West Dundee, IL)

    2011-07-26

    There is provided a method of making a polymer solution comprising polymerizing one or more monomer in a solvent, wherein said monomer comprises one or more ethylenically unsaturated monomer that is a multi-functional Michael donor, and wherein said solvent comprises 40% or more by weight, based on the weight of said solvent, one or more multi-functional Michael donor.

  5. Westergaard Solutions

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

    Westergaard Solutions - Sandia Energy Energy Search Icon Sandia Home Locations Contact Us Employee Locator Energy & Climate Secure & Sustainable Energy Future Stationary Power Energy Conversion Efficiency Solar Energy Wind Energy Water Power Supercritical CO2 Geothermal Natural Gas Safety, Security & Resilience of the Energy Infrastructure Energy Storage Nuclear Power & Engineering Grid Modernization Battery Testing Nuclear Fuel Cycle Defense Waste Management Programs Advanced

  6. Engineering Options Assessment Report: Nitrate Salt Waste Stream Processing

    SciTech Connect (OSTI)

    Anast, Kurt Roy

    2015-11-18

    This report examines and assesses the available systems and facilities considered for carrying out remediation activities on remediated nitrate salt (RNS) and unremediated nitrate salt (UNS) waste containers at Los Alamos National Laboratory (LANL). The assessment includes a review of the waste streams consisting of 60 RNS, 29 aboveground UNS, and 79 candidate belowground UNS containers that may need remediation. The waste stream characteristics were examined along with the proposed treatment options identified in the Options Assessment Report . Two primary approaches were identified in the five candidate treatment options discussed in the Options Assessment Report: zeolite blending and cementation. Systems that could be used at LANL were examined for housing processing operations to remediate the RNS and UNS containers and for their viability to provide repackaging support for remaining LANL legacy waste.

  7. Engineering Options Assessment Report. Nitrate Salt Waste Stream Processing

    SciTech Connect (OSTI)

    Anast, Kurt Roy

    2015-11-13

    This report examines and assesses the available systems and facilities considered for carrying out remediation activities on remediated nitrate salt (RNS) and unremediated nitrate salt (UNS) waste containers at Los Alamos National Laboratory (LANL). The assessment includes a review of the waste streams consisting of 60 RNS, 29 above-ground UNS, and 79 candidate below-ground UNS containers that may need remediation. The waste stream characteristics were examined along with the proposed treatment options identified in the Options Assessment Report . Two primary approaches were identified in the five candidate treatment options discussed in the Options Assessment Report: zeolite blending and cementation. Systems that could be used at LANL were examined for housing processing operations to remediate the RNS and UNS containers and for their viability to provide repackaging support for remaining LANL legacy waste.

  8. Waste Isolation Pilot Plant Nitrate Salt Bearing Waste Container

    Office of Environmental Management (EM)

    Nitrate Salt Bearing Waste Container Isolation Plan Prepared in Response to New Mexico Environment Department Administrative Order 05-20001 Issued May 20, 2014 1.0 INTRODUCTION The purpose of this document is to provide the Plan required by the New Mexico Environment Department (NMED) Administrative Order 05-20001 (Order) issued on May 20, 2014 to the U. S. Department of Energy (DOE) and Nuclear Waste Partnership LLC (NWP), collectively referred to as the Permittees. The Order, at paragraph 22,

  9. WIPP Nitrate Salt Bearing Waste Container Isolation Plan Implementation Update

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

    Nitrate Salt Bearing Waste Container Isolation Plan Implementation Update May 12, 2015 Panel 6 and Panel 7, Room 7 a. Rollback * Contamination Assessment-This prerequisite is complete and therefore status updates are no longer required. * Fixing/Decontamination Activities-Decontaminated equipment has been removed from Room 7 of Panel 7 to prepare for Room 7 closure activities. Remaining items in Panel 7, Room 7 include thirteen empty magnesium oxide racks, about 200 roof bolts, nine messenger

  10. REDUCTION OF ACIDITY OF NITRIC ACID SOLUTIONS BY USE OF FORMALDEHYDE

    DOE Patents [OSTI]

    Healy, T.V.

    1958-05-20

    A continuous method is described of concentrating by evaporation and reducing the nitrate ion content of an aqueous solution of metallic salts containing nitric acid not in excess of 8N. It consists of heating the solution and then passing formaldehyde into the heated solution to bring about decomposition of the nitric acid. The evolved gases containing NO are contacted countercurrently with an aqueous metal salt solution containing nitric acid in excess of 8N so as to bring about decomposition of the nitric acid and lower the normality to at least 8N, whereupon it is passed into the body of heated solution.

  11. Real time in situ detection of organic nitrates in atmospheric aerosols

    SciTech Connect (OSTI)

    Rollins, Andrew W.; Smith, Jared D.; Wilson, Kevin R.; Cohen, Ronald C.

    2010-06-11

    A new field instrument is described that quantifies total particle phase organic nitrates. The instrument is based on the thermal dissociation laser induced fluorescence (TD-LIF) method that thermally converts nitrates to NO2 which is then detected by LIF. This instrument is unique in its ability to provide fast sensitive measurements of particle phase organic nitrates, without interference from inorganic nitrate. Here we use it to quantify organic nitrates in SOA generated from high-NOx photooxidation of limonene, a-pinene, D-3-carene, and tridecane. In these experiments the organic nitrate moiety is observed to be 6-15percent of the total SOA mass, depending on the organic precursor.

  12. Effect of composition on the density of multi-component molten nitrate salts.

    SciTech Connect (OSTI)

    Bradshaw, Robert W.

    2009-12-01

    The density of molten nitrate salts was measured to determine the effects of the constituents on the density of multi-component mixtures. The molten salts consisted of various proportions of the nitrates of potassium, sodium, lithium and calcium. Density measurements ere performed using an Archimedean method and the results were compared to data reported in the literature for the individual constituent salts or simple combinations, such as the binary Solar Salt mixture of NaNO3 and KNO3. The addition of calcium nitrate generally ncreased density, relative to potassium nitrate or sodium nitrate, while lithium nitrate decreased density. The temperature dependence of density is described by a linear equation regardless of composition. The molar volume, and thereby, density of multi-component mixtures an be calculated as a function of temperature using a linear additivity rule based on the properties of the individual constituents.

  13. Low-melting point inorganic nitrate salt heat transfer fluid

    DOE Patents [OSTI]

    Bradshaw, Robert W.; Brosseau, Douglas A.

    2009-09-15

    A low-melting point, heat transfer fluid made of a mixture of four inorganic nitrate salts: 9-18 wt % NaNO.sub.3, 40-52 wt % KNO.sub.3, 13-21 wt % LiNO.sub.3, and 20-27 wt % Ca(NO.sub.3).sub.2. These compositions can have liquidus temperatures less than 100 C; thermal stability limits greater than 500 C; and viscosity in the range of 5-6 cP at 300 C; and 2-3 cP at 400 C.

  14. Laser-induced breakdown spectroscopic study of ammonium nitrate plasma

    SciTech Connect (OSTI)

    Hanif, M.; Salik, M.; Baig, M. A.

    2013-12-15

    We present the optical emission studies of the ammonium nitrate plasma produced by the fundamental (1064 nm) and second (532 nm) harmonics of a Q-switched Nd: YAG laser. The target material was placed in front of the laser beam in an open atmospheric air. The spectrum reveals numerous transitions of neutral nitrogen. We have studied the spatial behavior of the plasma temperature (T{sub e}) and electron number density (N{sub e}) determined using the Boltzmann plot method and Stark broadened line profiles, respectively. Besides, we have studied the variation of the plasma parameters as a function of the laser irradiance.

  15. Investigating In Situ Bioremediation Approaches for Sustained Uranium Immobilization Independent of Nitrate Reduction

    SciTech Connect (OSTI)

    Phelps, Tommy; Balkwill, David

    2006-06-01

    The daunting prospect of complete nitrate removal at DOE sites, such as the ERSP Oak Ridge Field Research Center (FRC), provides strong incentive to explore bioremediation strategies that will allow for uranium bioreduction and long-term stabilization in the presence of nitrate. The cost and effort required for complete nitrate removal from the FRC and similar DOE-contaminated sites may prove to be unworkable. For example, field tests of uranium bioreduction at the FRC have shown that nitrate levels rebound quickly and completely after cessation of active biostimulation.

  16. Mercuric iodate precipitation from radioiodine-containing off-gas scrubber solution

    DOE Patents [OSTI]

    Partridge, Jerry A. (Richland, WA); Bosuego, Gail P. (Richland, WA)

    1982-01-01

    Mercuric nitrate-nitric acid scrub solutions containing radioiodine may be reduced in volume without excessive loss of volatile iodine. The use of concentrated nitric acid during an evaporation process oxidizes the mercury-iodide complex to a less volatile mercuric iodate precipitate.

  17. The chemistry of plutonium(VI) in aqueous carbonate solutions

    SciTech Connect (OSTI)

    Stout, B.E.; Choppin, G.R. . Dept. of Chemistry); Sullivan, J.C. )

    1990-01-01

    The dynamic behavior of carbonate ion as a ligand that interacts with the hexavalent actinyl ions of U, Np, and Pu has been examined by {sup 13}C NMR. The first order rate parameter that describes the exchange between bulk solution and bound carbonate decreases with increasing pH. At a pH of 10.0, 25{degree}C, the respective values of k for the U(VI), Np(VI) and Pu(VI) complexes are 27.1 {plus minus} 0.3, 64.7 {plus minus} 3.3 and 706 {plus minus} 29. The variation of k with temperature was used to calculate the values of {Delta}H{sup +} = 53 and 42 kJ/M; and {Delta}S{sup +} = {minus}40 and {minus}71 J/M-K for the uranyl and neptunyl systems, respectively. A plausible reaction scheme for the exchange reaction is considered. The influence of these slow carbonate exchange reactions on selected electron transfer reactions is noted. 19 refs., 4 figs., 2 tabs.

  18. Stainless steel corrosion by molten nitrates : analysis and lessons learned.

    SciTech Connect (OSTI)

    Kruizenga, Alan Michael

    2011-09-01

    A secondary containment vessel, made of stainless 316, failed due to severe nitrate salt corrosion. Corrosion was in the form of pitting was observed during high temperature, chemical stability experiments. Optical microscopy, scanning electron microscopy and energy dispersive spectroscopy were all used to diagnose the cause of the failure. Failure was caused by potassium oxide that crept into the gap between the primary vessel (alumina) and the stainless steel vessel. Molten nitrate solar salt (89% KNO{sub 3}, 11% NaNO{sub 3} by weight) was used during chemical stability experiments, with an oxygen cover gas, at a salt temperature of 350-700 C. Nitrate salt was primarily contained in an alumina vessel; however salt crept into the gap between the alumina and 316 stainless steel. Corrosion occurred over a period of approximately 2000 hours, with the end result of full wall penetration through the stainless steel vessel; see Figures 1 and 2 for images of the corrosion damage to the vessel. Wall thickness was 0.0625 inches, which, based on previous data, should have been adequate to avoid corrosion-induced failure while in direct contact with salt temperature at 677 C (0.081-inch/year). Salt temperatures exceeding 650 C lasted for approximately 14 days. However, previous corrosion data was performed with air as the cover gas. High temperature combined with an oxygen cover gas obviously drove corrosion rates to a much higher value. Corrosion resulted in the form of uniform pitting. Based on SEM and EDS data, pits contained primarily potassium oxide and potassium chromate, reinforcing the link between oxides and severe corrosion. In addition to the pitting corrosion, a large blister formed on the side wall, which was mainly composed of potassium, chromium and oxygen. All data indicated that corrosion initiated internally and moved outward. There was no evidence of intergranular corrosion nor were there any indication of fast pathways along grain boundaries. Much of the pitting occurred near welds; however this was the hottest region in the chamber. Pitting was observed up to two inches above the weld, indicating independence from weld effects.

  19. Viscosity of multi-component molten nitrate salts : liquidus to 200 degrees C.

    SciTech Connect (OSTI)

    Bradshaw, Robert W.

    2010-03-01

    The viscosity of molten salts comprising ternary and quaternary mixtures of the nitrates of sodium, potassium, lithium and calcium was determined experimentally. Viscosity was measured over the temperature range from near the relatively low liquidus temperatures of he individual mixtures to 200C. Molten salt mixtures that do not contain calcium nitrate exhibited relatively low viscosity and an Arrhenius temperature dependence. Molten salt mixtures that contained calcium nitrate were relatively more viscous and viscosity increased as the roportion of calcium nitrate increased. The temperature dependence of viscosity of molten salts containing calcium nitrate displayed curvature, rather than linearity, when plotted in Arrhenius format. Viscosity data for these mixtures were correlated by the Vogel-Fulcher- ammann-Hesse equation.

  20. Hydroxylamine Nitrate Decomposition under Non-radiological Conditions

    SciTech Connect (OSTI)

    McFarlane, Joanna; Delmau, Laetitia Helene; DePaoli, David W.; Mattus, Catherine H.; Phelps, Clarice E.; Roach, Benjamin D.

    2015-07-01

    Hydroxylamine nitrate (HAN) is used to reduce Pu(IV) to Pu(III) in the separation of plutonium from uranium. HAN becomes unstable under certain conditions and has been known to explode, causing injury to humans including death. Hence, it is necessary to deactivate HAN once the reduction of plutonium is finished. This report reviews what is known about the chemistry of HAN and various methods to achieve a safe decomposition. However, there are areas where more information is needed to make a decision about the handling of HAN in reprocessing of nuclear fuel. Experiments have demonstrated a number of non-radiolytic ways to safely decompose HAN, including heating in HNO3, photolytic oxidation in the presence of H2O2, and the addition of a metal such as Fe(III) that will oxidize the HAN.

  1. Revised RCRA closure plan for the Interim Drum Yard (S-030) at the Oak Ridge Y-12 Plant, Oak Ridge, Tennessee

    SciTech Connect (OSTI)

    Smith, C.M.

    1994-09-01

    The Interim Drum Yard (IDY) facility is a containerized waste storage area located in the Y-12 exclusion area. It was used to store waste materials which are regulated by RCRA (Resource Conservation and Recovery Act); uranyl nitrate solutions were also stored there. The closure plan outlines the actions required to achieve closure of IDY and is being submitted in accordance with TN Rule 1200-1-11.05(7) and 40 CFR 265.110.

  2. Ab initio calculations of singlet and triplet excited states of chlorine nitrate and nitric acid

    SciTech Connect (OSTI)

    Grana, A.M.; Head-Gordon, M. |; Lee, T.J.

    1995-03-16

    Ab initio calculations of vertical excitations to single and triplet excited states of chlorine nitrate and nitric acid are reported, using the CIS, CIS(D), and CCSD methods. The effects of basis set composition and calculational methods are investigated. The nature of the electronic transitions are examined by decomposing the difference density into the sum of detachment and attachment densities. Counterparts for the three lowest singlet excited states of nitric acid survive relatively unperturbed in chlorine nitrate, while other low lying singlet states of chlorine nitrate appear to be directly dissociative in the CIO chromophore. These results suggest an assignment of the two main peaks in the experimental chlorine nitrate absorption spectrum. In addition, triplet vertical excitations and the lowest optimized triplet geometries of both molecules are studied. 70 refs., 2 figs., 6 tabs.

  3. EP-AREAG-PLAN-1248, R.0 TA-54 Area G Nitrate-Salt Waste Container...

    Office of Environmental Management (EM)

    EP-AREAG-PLAN-1248, R.0 TA-54 Area G Nitrate-Salt Waste Container Response Instructions Effective Date: 5282014 The Responsible Manager has determined that the following...

  4. EMRTC Report RF 10-13: Application to LANL Evaporator Nitrate...

    Office of Environmental Management (EM)

    and recommendation. Conclusions: 1. Nitrate salts not yet remediated having no free liquid should be mixed with at least 1.2 volumes of Kitty LitterZeolite clay per...

  5. Technical Area (TA)-54 Area G Nitrate-Salt Waste Container Response

    Office of Environmental Management (EM)

    Instructions | Department of Energy Technical Area (TA)-54 Area G Nitrate-Salt Waste Container Response Instructions Technical Area (TA)-54 Area G Nitrate-Salt Waste Container Response Instructions This document was used to determine facts and conditions during the Department of Energy Accident Investigation Board's investigation into the radiological release event at the Waste Isolation Pilot Plant. Additional documents referenced and listed in the Phase 2 Radiological Release Event at the

  6. In situ mobility of uranium in the presence of nitrate following

    Office of Scientific and Technical Information (OSTI)

    sulfate-reducing conditions (Journal Article) | DOE PAGES Published Article: In situ mobility of uranium in the presence of nitrate following sulfate-reducing conditions « Prev Next » Title: In situ mobility of uranium in the presence of nitrate following sulfate-reducing conditions Authors: Paradis, Charles J. ; Jagadamma, Sindhu ; Watson, David B. ; McKay, Larry D. ; Hazen, Terry C. ; Park, Melora ; Istok, Jonathan D. Publication Date: 2016-04-01 OSTI Identifier: 1237977 Grant/Contract

  7. Analytical Chemistry and Materials Characterization Results for Debris Recovered from Nitrate Salt Waste Drum S855793

    SciTech Connect (OSTI)

    Martinez, Patrick Thomas; Chamberlin, Rebecca M.; Schwartz, Daniel S.; Worley, Christopher Gordon; Garduno, Katherine; Lujan, Elmer J. W.; Borrego, Andres Patricio; Castro, Alonso; Colletti, Lisa Michelle; Fulwyler, James Brent; Holland, Charlotte S.; Keller, Russell C.; Klundt, Dylan James; Martinez, Alexander; Martin, Frances Louise; Montoya, Dennis Patrick; Myers, Steven Charles; Porterfield, Donivan R.; Schake, Ann Rene; Schappert, Michael Francis; Soderberg, Constance B.; Spencer, Khalil J.; Stanley, Floyd E.; Thomas, Mariam R.; Townsend, Lisa Ellen; Xu, Ning

    2015-09-16

    Solid debris was recovered from the previously-emptied nitrate salt waste drum S855793. The bulk sample was nondestructively assayed for radionuclides in its as-received condition. Three monoliths were selected for further characterization. Two of the monoliths, designated Specimen 1 and 3, consisted primarily of sodium nitrate and lead nitrate, with smaller amounts of lead nitrate oxalate and lead oxide by powder x-ray diffraction. The third monolith, Specimen 2, had a complex composition; lead carbonate was identified as the predominant component, and smaller amounts of nitrate, nitrite and carbonate salts of lead, magnesium and sodium were also identified. Microfocused x-ray fluorescence (MXRF) mapping showed that lead was ubiquitous throughout the cross-sections of Specimens 1 and 2, while heteroelements such as potassium, calcium, chromium, iron, and nickel were found in localized deposits. MXRF examination and destructive analysis of fragments of Specimen 3 showed elevated concentrations of iron, which were broadly distributed through the sample. With the exception of its high iron content and low carbon content, the chemical composition of Specimen 3 was within the ranges of values previously observed in four other nitrate salt samples recovered from emptied waste drums.

  8. Laboratory study of nitrate photolysis in Antarctic snow. I. Observed quantum yield, domain of photolysis, and secondary chemistry

    SciTech Connect (OSTI)

    Meusinger, Carl; Johnson, Matthew S. [Department of Chemistry, University of Copenhagen, Copenhagen (Denmark); Berhanu, Tesfaye A.; Erbland, Joseph; Savarino, Joel, E-mail: jsavarino@lgge.obs.ujf-grenoble.fr [Univ. Grenoble Alpes, LGGE, F-38000 Grenoble (France); CNRS, LGGE, F-38000 Grenoble (France)

    2014-06-28

    Post-depositional processes alter nitrate concentration and nitrate isotopic composition in the top layers of snow at sites with low snow accumulation rates, such as Dome C, Antarctica. Available nitrate ice core records can provide input for studying past atmospheres and climate if such processes are understood. It has been shown that photolysis of nitrate in the snowpack plays a major role in nitrate loss and that the photolysis products have a significant influence on the local troposphere as well as on other species in the snow. Reported quantum yields for the main reaction spans orders of magnitude apparently a result of whether nitrate is located at the air-ice interface or in the ice matrix constituting the largest uncertainty in models of snowpack NO{sub x} emissions. Here, a laboratory study is presented that uses snow from Dome C and minimizes effects of desorption and recombination by flushing the snow during irradiation with UV light. A selection of UV filters allowed examination of the effects of the 200 and 305nm absorption bands of nitrate. Nitrate concentration and photon flux were measured in the snow. The quantum yield for loss of nitrate was observed to decrease from 0.44 to 0.003 within what corresponds to days of UV exposure in Antarctica. The superposition of photolysis in two photochemical domains of nitrate in snow is proposed: one of photolabile nitrate, and one of buried nitrate. The difference lies in the ability of reaction products to escape the snow crystal, versus undergoing secondary (recombination) chemistry. Modeled NO{sub x} emissions may increase significantly above measured values due to the observed quantum yield in this study. The apparent quantum yield in the 200nm band was found to be ?1%, much lower than reported for aqueous chemistry. A companion paper presents an analysis of the change in isotopic composition of snowpack nitrate based on the same samples as in this study.

  9. Laboratory study of nitrate photolysis in Antarctic snow. II. Isotopic effects and wavelength dependence

    SciTech Connect (OSTI)

    Berhanu, Tesfaye A.; Erbland, Joseph; Savarino, Jol [Laboratoire de Glaciologie et Gophysique de lEnvironnement, CNRS, F-38041 Grenoble (France); Univ. Grenoble Alpes, LGGE, F-38041 Grenoble (France); Meusinger, Carl; Johnson, Matthew S. [Copenhagen Center for Atmospheric Research (CCAR), Department of Chemistry, University of Copenhagen, Copenhagen (Denmark); Jost, Rmy [Laboratoire de Interdisciplinaire de Physique (LIPHY) Univ. de Grenoble, Grenoble (France); Bhattacharya, S. K. [Research Center for Environmental Changes, Academia Sinica, Nangang, Taipei 115, Taiwan (China)

    2014-06-28

    Atmospheric nitrate is preserved in Antarctic snow firn and ice. However, at low snow accumulation sites, post-depositional processes induced by sunlight obscure its interpretation. The goal of these studies (see also Paper I by Meusinger et al. [Laboratory study of nitrate photolysis in Antarctic snow. I. Observed quantum yield, domain of photolysis, and secondary chemistry, J. Chem. Phys. 140, 244305 (2014)]) is to characterize nitrate photochemistry and improve the interpretation of the nitrate ice core record. Naturally occurring stable isotopes in nitrate ({sup 15}N, {sup 17}O, and {sup 18}O) provide additional information concerning post-depositional processes. Here, we present results from studies of the wavelength-dependent isotope effects from photolysis of nitrate in a matrix of natural snow. Snow from Dome C, Antarctica was irradiated in selected wavelength regions using a Xe UV lamp and filters. The irradiated snow was sampled and analyzed for nitrate concentration and isotopic composition (?{sup 15}N, ?{sup 18}O, and ?{sup 17}O). From these measurements an average photolytic isotopic fractionation of {sup 15}? = (?15 1.2) was found for broadband Xe lamp photolysis. These results are due in part to excitation of the intense absorption band of nitrate around 200 nm in addition to the weaker band centered at 305 nm followed by photodissociation. An experiment with a filter blocking wavelengths shorter than 320 nm, approximating the actinic flux spectrum at Dome C, yielded a photolytic isotopic fractionation of {sup 15}? = (?47.9 6.8), in good agreement with fractionations determined by previous studies for the East Antarctic Plateau which range from ?40 to ?74.3. We describe a new semi-empirical zero point energy shift model used to derive the absorption cross sections of {sup 14}NO{sub 3}{sup ?} and {sup 15}NO{sub 3}{sup ?} in snow at a chosen temperature. The nitrogen isotopic fractionations obtained by applying this model under the experimental temperature as well as considering the shift in width and center well reproduced the values obtained in the laboratory study. These cross sections can be used in isotopic models to reproduce the stable isotopic composition of nitrate found in Antarctic snow profiles.

  10. Randa Energy Solutions LLC R A Energy Solutions | Open Energy...

    Open Energy Info (EERE)

    LLC R A Energy Solutions Jump to: navigation, search Name: Randa Energy Solutions, LLC (R&A Energy Solutions) Place: North Ridgeville, Ohio Zip: 44039 Product: String...

  11. Baseload Nitrate Salt Central Receiver Power Plant Design Final Report

    SciTech Connect (OSTI)

    Tilley, Drake; Kelly, Bruce; Burkholder, Frank

    2014-12-12

    The objectives of the work were to demonstrate that a 100 MWe central receiver plant, using nitrate salt as the receiver coolant, thermal storage medium, and heat transport fluid in the steam generator, can 1) operate, at full load, for 6,400 hours each year using only solar energy, and 2) satisfy the DOE levelized energy cost goal of $0.09/kWhe (real 2009 $). To achieve these objectives the work incorporated a large range of tasks relating to many different aspects of a molten salt tower plant. The first Phase of the project focused on developing a baseline design for a Molten Salt Tower and validating areas for improvement. Tasks included a market study, receiver design, heat exchanger design, preliminary heliostat design, solar field optimization, baseline system design including PFDs and P&IDs and detailed cost estimate. The baseline plant met the initial goal of less than $0.14/kWhe, and reinforced the need to reduce costs in several key areas to reach the overall $0.09/kWhe goal. The major improvements identified from Phase I were: 1) higher temperature salt to improve cycle efficiency and reduce storage requirements, 2) an improved receiver coating to increase the efficiency of the receiver, 3) a large receiver design to maximize storage and meet the baseload hours objective, and 4) lower cost heliostat field. The second Phase of the project looked at advancing the baseline tower with the identified improvements and included key prototypes. To validate increasing the standard solar salt temperature to 600 °C a dynamic test was conducted at Sandia. The results ultimately proved the hypothesis incorrect and showed high oxide production and corrosion rates. The results lead to further testing of systems to mitigate the oxide production to be able to increase the salt temperature for a commercial plant. Foster Wheeler worked on the receiver design in both Phase I and Phase II looking at both design and lowering costs utilizing commercial fossil boiler manufacturing. The cost and design goals for the project were met with this task, but the most interesting results had to do with defining the failure modes and looking at a “shakedown analysis” of the combined creep-fatigue failure. A separate task also looked at improving the absorber coatings on the receiver tubes that would improve the efficiency of the receiver. Significant progress was made on developing a novel paint with a high absorptivity that was on par with the current Pyromark, but shows additional potential to be optimized further. Although the coating did not meet the emissivity goals, preliminary testing the new paint shows potential to be much more durable, and potential to improve the receiver efficiency through a higher average absorptivity over the lifetime. Additional coatings were also designed and modeled results meet the project goals, but were not tested. Testing for low cycle fatigue of the full length receiver tubes was designed and constructed, but is still currently undergoing testing. A novel small heliostat was developed through an extensive brainstorming and down select. The concept was then detailed further with inputs from component testing and eventually a full prototype was built and tested. This task met or exceeded the accuracy and structure goals and also beat the cost goal. This provides a significant solar field costs savings for Abengoa that will be developed further to be used in future commercial plants. Ultimately the $0.09/kWhe (real 2009 $) and 6,400 hours goals of the project were met.

  12. Solution deposition assembly

    DOE Patents [OSTI]

    Roussillon, Yann; Scholz, Jeremy H; Shelton, Addison; Green, Geoff T; Utthachoo, Piyaphant

    2014-01-21

    Methods and devices are provided for improved deposition systems. In one embodiment of the present invention, a deposition system is provided for use with a solution and a substrate. The system comprises of a solution deposition apparatus; at least one heating chamber, at least one assembly for holding a solution over the substrate; and a substrate curling apparatus for curling at least one edge of the substrate to define a zone capable of containing a volume of the solution over the substrate. In another embodiment of the present invention, a deposition system for use with a substrate, the system comprising a solution deposition apparatus; at heating chamber; and at least assembly for holding solution over the substrate to allow for a depth of at least about 0.5 microns to 10 mm.

  13. Biological Redox Cycling Of Iron In Nontronite And Its Potential Application In Nitrate Removal

    SciTech Connect (OSTI)

    Zhao, Linduo; Dong, Hailiang; Kukkadapu, Ravi K.; Zeng, Qiang; Edelmann, Richard E.; Pentrak, Martin; Agrawal, Abinash

    2015-05-05

    Redox cycling of structural Fe in phyllosilicates provides a potential method to remediate nitrate contamination in natural environment. Past research has only studied chemical redox cycles or a single biologically mediated redox cycle of Fe in phyllosilicates. The objective of this research was to study three microbially driven redox cycles of Fe in one phyllosilicate, nontronite (NAu-2). During the reduction phase structural Fe(III) in NAu-2 served as electron acceptor, lactate as electron donor, AQDS as electron shuttle, and dissimilatory Fe(III)-reducing bacteria Shewanella putrefaciens CN32 as mediator in bicarbonate-buffered and PIPES-buffered media. During the oxidation phase, biogenic Fe(II) served an electron donor, nitrate as electron acceptor, and nitrate-dependent Fe(II)-oxidizing bacteria Pseudogulbenkiania sp. strain 2002 as mediator in the same media. For all three cycles, structural Fe in NAu-2 was able to reversibly undergo 3 redox cycles without significant reductive or oxidative dissolution. X-ray diffraction and scanning and transmission electron microscopy revealed that NAu-2 was the dominant residual mineral throughout the 3 redox cycles with some dissolution textures but no significant secondary mineralization. Mssbauer spectroscopy revealed that Fe(II) in bio-reduced samples likely occurred in two distinct environments, at edges and the interior of the NAu-2 structure. Nitrate was completely reduced to nitrogen gas under both buffer conditions and this extent and rate did not change with Fe redox cycles. Mssbauer spectroscopy further revealed that nitrate reduction was coupled to predominant/preferred oxidation of edge Fe(II). These results suggest that structural Fe in phyllosilicates may represent a renewable source to continuously remove nitrate in natural environments.

  14. Mixed oxide solid solutions

    DOE Patents [OSTI]

    Magno, Scott (Dublin, CA); Wang, Ruiping (Fremont, CA); Derouane, Eric (Liverpool, GB)

    2003-01-01

    The present invention is a mixed oxide solid solution containing a tetravalent and a pentavalent cation that can be used as a support for a metal combustion catalyst. The invention is furthermore a combustion catalyst containing the mixed oxide solid solution and a method of making the mixed oxide solid solution. The tetravalent cation is zirconium(+4), hafnium(+4) or thorium(+4). In one embodiment, the pentavalent cation is tantalum(+5), niobium(+5) or bismuth(+5). Mixed oxide solid solutions of the present invention exhibit enhanced thermal stability, maintaining relatively high surface areas at high temperatures in the presence of water vapor.

  15. TVA- Solar Solutions Initiative

    Broader source: Energy.gov [DOE]

    Solar Solutions Initiative (SSI) is a pilot program that offers additional financial incentives for Solar PV systems participating in the Renewable Standard Offer program. Applications for new...

  16. Reduction of Nitrate in Shewanella oneidensis depends on atypical NAP and

    Office of Scientific and Technical Information (OSTI)

    NRF systems with NapB as a preferred electron transport protein from CymA to NapA (Journal Article) | SciTech Connect Reduction of Nitrate in Shewanella oneidensis depends on atypical NAP and NRF systems with NapB as a preferred electron transport protein from CymA to NapA Citation Details In-Document Search Title: Reduction of Nitrate in Shewanella oneidensis depends on atypical NAP and NRF systems with NapB as a preferred electron transport protein from CymA to NapA In the genome of

  17. EMRTC Report RF 10-13: Application to LANL Evaporator Nitrate Salts

    Office of Environmental Management (EM)

    Amount of Zeolite Required to Meet the Constraints Established by the EMRTC Report RF 10-13: Application to LANL Evaporator Nitrate Salts 5/8/2012 LANL-Carlsbad Office Difficult Waste Team P2010-3306 Amount of Zeolite Required to Meet the Constraints Established by the EMRTC Report RF 10- 13: Application to LANL Evaporator Nitrate Salts 2 Purpose: The following document was developed in support of the Los Alamos National Laboratory Transuranic Program (LTP) by the LANL-Carlsbad Office, Difficult

  18. Solvent wash solution

    DOE Patents [OSTI]

    Neace, James C. (Blackville, SC)

    1986-01-01

    Process for removing diluent degradation products from a solvent extraction solution, which has been used to recover uranium and plutonium from spent nuclear fuel. A wash solution and the solvent extraction solution are combined. The wash solution contains (a) water and (b) up to about, and including, 50 volume percent of at least one-polar water-miscible organic solvent based on the total volume of the water and the highly-polar organic solvent. The wash solution also preferably contains at least one inorganic salt. The diluent degradation products dissolve in the highly-polar organic solvent and the organic solvent extraction solvent do not dissolve in the highly-polar organic solvent. The highly-polar organic solvent and the extraction solvent are separated.

  19. Solvent wash solution

    DOE Patents [OSTI]

    Neace, J.C.

    1984-03-13

    A process is claimed for removing diluent degradation products from a solvent extraction solution, which has been used to recover uranium and plutonium from spent nuclear fuel. A wash solution and the solvent extraction solution are combined. The wash solution contains (a) water and (b) up to about, and including, 50 vol % of at least one-polar water-miscible organic solvent based on the total volume of the water and the highly-polar organic solvent. The wash solution also preferably contains at least one inorganic salt. The diluent degradation products dissolve in the highly-polar organic solvent and the organic solvent extraction solvent do not dissolve in the highly-polar organic solvent. The highly-polar organic solvent and the extraction solvent are separated.

  20. Dispersant solutions for dispersing hydrocarbons

    DOE Patents [OSTI]

    Tyndall, Richard L. (Clinton, TN)

    1997-01-01

    A dispersant solution includes a hydrocarbon dispersing solution derived from a bacterium from ATCC 75527, ATCC 75529, or ATCC 55638.

  1. Dispersant solutions for dispersing hydrocarbons

    DOE Patents [OSTI]

    Tyndall, R.L.

    1997-03-11

    A dispersant solution includes a hydrocarbon dispersing solution derived from a bacterium from ATCC 75527, ATCC 75529, or ATCC 55638.

  2. Sodium nitrate containing mixture for producing ceramic-glass-ceramic seal by microwave heating

    DOE Patents [OSTI]

    Blake, R.D.; Meek, T.T.

    1984-10-10

    A mixture for, and method of using such a mixture, for producing a ceramic-glass-ceramic seal by the use of microwave energy are disclosed, wherein the mixture comprises a glass sealing material, a coupling agent, and an oxidizer. The seal produced exhibits greater strength due to its different microstructure. Sodium nitrate is the most preferred oxidizer.

  3. [La(UO{sub 2})V{sub 2}O{sub 7}][(UO{sub 2})(VO{sub 4})] the first lanthanum uranyl-vanadate with structure built from two types of sheets based upon the uranophane anion-topology

    SciTech Connect (OSTI)

    Mer, A.; Obbade, S.; Rivenet, M.; Renard, C.; Abraham, F.

    2012-01-15

    The new lanthanum uranyl vanadate divanadate, [La(UO{sub 2})V{sub 2}O{sub 7}][(UO{sub 2})(VO{sub 4})] was obtained by reaction at 800 Degree-Sign C between lanthanum chloride, uranium oxide (U{sub 3}O{sub 8}) and vanadium oxide (V{sub 2}O{sub 5}) and the structure was determined from single-crystal X-ray diffraction data. This compound crystallizes in the orthorhombic system with space group P2{sub 1}2{sub 1}2{sub 1} and unit-cell parameters a=6.9470(2) A, b=7.0934(2) A, c=25.7464(6) A, V=1268.73(5) A{sup 3}, Z=4. A full matrix least-squares refinement yielded R{sub 1}=0.0219 for 5493 independent reflections. The crystal structure is characterized by the stacking of uranophane-type sheets {sup 2}{sub {infinity}}[(UO{sub 2})(VO{sub 4})]{sup -} and double layers {sup 2}{sub {infinity}}[La(UO{sub 2})(V{sub 2}O{sub 7})]{sup +} connected through La-O bonds involving the uranyl oxygen of the uranyl-vanadate sheets. The double layers result from the connection of two {sup 2}{sub {infinity}}[La(UO{sub 2})(VO{sub 4}){sub 2}]{sup -} sheets derived from the uranophane anion-topology by replacing half of the uranyl ions by lanthanum atoms and connected through the formation of divanadate entities. - Graphical abstract: A view of the three-dimensional structure of [La(UO{sub 2})V{sub 2}O{sub 7}][(UO{sub 2})(VO{sub 4})]. Highlights: Black-Right-Pointing-Pointer New lanthanum uranyl vanadate divanadate has been synthesized. Black-Right-Pointing-Pointer Structure was determined from single-crystal X-ray diffraction data. Black-Right-Pointing-Pointer Structure is characterized by uranophane-type sheets and double layers {sup 2}{sub {infinity}}[La(UO{sub 2})(V{sub 2}O{sub 7})]{sup +}.

  4. Thermodynamic and structural description of europium complexation in 1-octanol solution

    SciTech Connect (OSTI)

    Charbonnel, M.C.; Vu, T.H.; Boubals, N.; Couston, L.

    2008-07-01

    Polydentate N-bearing ligands such as bis-triazinyl-pyridines (BTPS) are interesting extractants for actinide(III)/lanthanide(III) separation. A description of europium complexation in 1-octanol solutions was undertaken to enhance the knowledge of the extraction mechanisms. Time- Resolved Laser-Induced Fluorescence (TRLIF) spectroscopy allows determination of the first solvation shell for europium(III) nitrate, chloride, and perchlorate with different amounts of water. Europium nitrate complexation by iPr-BTP was then studied by TRLIF and microcalorimetry; the stability constant related to the formation of Eu(BTP){sub 3}{sup 3+} is similar by both techniques (log {beta}{sub 3} = 11.3 {+-} 0.5). The difference of solvation of the cation seems to have an influence on the thermodynamic properties related to the complexation with organic ligands. (authors)

  5. Solution mass measurement

    SciTech Connect (OSTI)

    Ford, W.; Marshall, R.S.; Osborn, L.C.; Picard, R.; Thomas, C.C. Jr.

    1982-07-01

    This report describes the efforts to develop and demonstrate a solution mass measurement system for use at the Los Alamos Plutonium Facility. Because of inaccuracy of load cell measurements, our major effort was directed towards the pneumatic bubbler tube. The differential pressure between the air inlet to the bubbler tube and the glovebox interior is measured and is proportional to the solution mass in the tank. An inexpensive, reliable pressure transducer system for measuring solution mass in vertical, cylindrical tanks was developed, tested, and evaluated in a laboratory test bed. The system can withstand the over- and underpressures resulting from solution transfer operations and can prevent solution backup into the measurement pressure transducer during transfers. Drifts, noise, quantization error, and other effects limit the accuracy to 30 g. A transportable calibration system using a precision machined tank, pneumatic bubbler tubes, and a Ruska DDR 6000 electromanometer was designed, fabricated, tested, and evaluated. Resolution of the system is +-3.5 g out of 50 kg. The calibration error is 5 g, using room-temperature water as the calibrating fluid. Future efforts will be directed towards in-plant test and evaluation of the tank measurement systems. 16 figures, 3 tables.

  6. Fissile solution measurement apparatus

    DOE Patents [OSTI]

    Crane, T.W.; Collinsworth, P.R.

    1984-06-11

    An apparatus for determining the content of a fissile material within a solution by detecting delayed fission neutrons emitted by the fissile material after it is temporarily irradiated by a neutron source. The apparatus comprises a container holding the solution and having a portion defining a neutron source cavity centrally disposed within the container. The neutron source cavity temporarily receives the neutron source. The container has portions defining a plurality of neutron detector ports that form an annular pattern and surround the neutron source cavity. A plurality of neutron detectors count delayed fission neutrons emitted by the fissile material. Each neutron detector is located in a separate one of the neutron detector ports.

  7. Options assessment report: Treatment of nitrate salt waste at Los Alamos National Laboratory

    SciTech Connect (OSTI)

    Robinson, Bruce Alan; Stevens, Patrice Ann

    2015-09-16

    This report documents the methodology used to select a method of treatment for the remediated nitrate salt (RNS) and unremediated nitrate salt (UNS) waste containers at Los Alamos National Laboratory (LANL). The method selected should treat the containerized waste in a manner that renders the waste safe and suitable for transport and final disposal in the Waste Isolation Pilot Plant (WIPP) repository, under specifications listed in the WIPP Waste Acceptance Criteria (DOE/CBFO, 2013). LANL recognized that the results must be thoroughly vetted with the New Mexico Environment Department (NMED) and the a modification to the LANL Hazardous Waste Facility Permit is a necessary step before implementation of this or any treatment option. Likewise, facility readiness and safety basis approvals must be received from the Department of Energy (DOE). This report presents LANL's preferred option, and the documentation of the process for reaching the recommended treatment option for RNS and UNS waste, and is presented for consideration by NMED and DOE.

  8. DWPF coupled feed flowsheet material balance with batch one sludge and copper nitrate catalyst

    SciTech Connect (OSTI)

    Choi, A.S.

    1993-09-28

    The SRTC has formally transmitted a recommendation to DWPF to replace copper formate with copper nitrate as the catalyst form during precipitate hydrolysis [1]. The SRTC was subsequently requested to formally document the technical bases for the recommendation. A memorandum was issued on August 23, 1993 detailing the activities (and responsible individuals) necessary to address the impact of this change in catalyst form on process compatibility, safety, processibility environmental impact and product glass quality [2]. One of the activities identified was the preparation of a material balance in which copper nitrate is substituted for copper formate and the identification of key comparisons between this material balance and the current Batch 1 sludge -- Late Wash material balance [3].

  9. Building Solutions | Open Energy Information

    Open Energy Info (EERE)

    Building Solutions Jump to: navigation, search Name: Building Solutions Place: California Sector: Efficiency Product: California-based energy efficiency contractor and consultancy....

  10. Soy Solutions | Open Energy Information

    Open Energy Info (EERE)

    Solutions Jump to: navigation, search Name: Soy Solutions Place: Milford, Iowa Zip: 51351 Product: Manufacturer and distributor of 100 percent Soy-Based Biodiesel References: Soy...

  11. Enspiria Solutions | Open Energy Information

    Open Energy Info (EERE)

    Page Edit with form History Enspiria Solutions Jump to: navigation, search Name: Enspiria Solutions Place: Greenwood Village, Colorado Sector: Services Product: Greenwood...

  12. Powerit Solutions | Open Energy Information

    Open Energy Info (EERE)

    Powerit Solutions Jump to: navigation, search Name: Powerit Solutions Address: 568 First Ave South Place: Seattle, Washington Zip: 98104 Region: Pacific Northwest Area Sector:...

  13. Building America Solution Center Webinar

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

    Building America Solution Center Webinar July 22, 2015 Put New Tools and Content on the Building America Solution Center to Work for You CHRISSI ANTONOPOULOS Pacific NW National ...

  14. Sol Solution | Open Energy Information

    Open Energy Info (EERE)

    Solution Jump to: navigation, search Name: Sol Solution Place: Los Gatos, California Zip: 95030 Region: Bay Area Sector: Solar Product: Rainbow Concentrator, Current matching...

  15. Aqueous nitrate waste treatment: Technology comparison, cost/benefit, and market analysis

    SciTech Connect (OSTI)

    Not Available

    1994-01-01

    The purpose of this analysis is to provide information necessary for the Department of Energy (DOE) to evaluate the practical utility of the Nitrate to Ammonia and Ceramic or Glass (NAC/NAG/NAX) process, which is under development in the Oak Ridge National Laboratory. The NAC/NACx/NAX process can convert aqueous radioactive nitrate-laden waste to a glass, ceramic, or grout solid waste form. The tasks include, but are not limited to, the following: Identify current commercial technologies to meet hazardous and radiological waste disposal requirements. The technologies may be thermal or non-thermal but must be all inclusive (i.e., must convert a radionuclide-containing nitrate waste with a pH around 12 to a stable form that can be disposed at permitted facilities); evaluate and compare DOE-sponsored vitrification, grouting, and minimum additive waste stabilization projects for life-cycle costs; compare the technologies above with respect to material costs, capital equipment costs, operating costs, and operating efficiencies. For the NAC/NAG/NAX process, assume aluminum reactant is government furnished and ammonia gas may be marketed; compare the identified technologies with respect to frequency of use within DOE for environmental management applications with appropriate rationale for use; Assess the potential size of the DOE market for the NAC/NAG/NAX process; assess and off-gas issues; and compare with international technologies, including life-cycle estimates.

  16. TREATMENT TESTS FOR EX SITU REMOVAL OF CHROMATE & NITRATE & URANIUM (VI) FROM HANFORD (100-HR-3) GROUNDWATER FINAL REPORT

    SciTech Connect (OSTI)

    BECK MA; DUNCAN JB

    1994-01-03

    This report describes batch and ion exchange column laboratory scale studies investigating ex situ methods to remove chromate (chromium [VI]), nitrate (NO{sub 3}{sup -}) and uranium (present as uranium [VI]) from contaminated Hanford site groundwaters. The technologies investigated include: chemical precipitation or coprecipitation to remove chromate and uranium; and anion exchange to remove chromate, uranium and nitrate. The technologies investigated were specified in the 100-HR-3 Groundwater Treatability Test Plan. The method suggested for future study is anion exchange.

  17. SCADA Engineering Solutions

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

    Engineering Solutions - Sandia Energy Energy Search Icon Sandia Home Locations Contact Us Employee Locator Energy & Climate Secure & Sustainable Energy Future Stationary Power Energy Conversion Efficiency Solar Energy Wind Energy Water Power Supercritical CO2 Geothermal Natural Gas Safety, Security & Resilience of the Energy Infrastructure Energy Storage Nuclear Power & Engineering Grid Modernization Battery Testing Nuclear Fuel Cycle Defense Waste Management Programs Advanced

  18. Building America Solution Center

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

    Solution Center 2014 Building Technologies Office Peer Review Michael Baechler, michael.baechler@pnnl.gov Pacific Northwest National Laboratory Project Summary Timeline: Start date: October 2011 Planned end date: Ongoing Key Milestones 1. Launch supporting Energy Star, January 2013 2. Zero Energy Ready Home launch, June 2014 3. Existing home launch, winter 2015 Budget: Total DOE $ to date: $2,604,000 Total future DOE $: $4,500,000 (2 additional years development - 3 years of app and content

  19. Conceptual designs of NDA instruments for the NRTA system at the Rokkasho Reprocessing Plant

    SciTech Connect (OSTI)

    Li, T.K.; Klosterbuer, S.F.; Menlove, H.O.

    1996-09-01

    The authors are studying conceptual designs of selected nondestructive assay (NDA) instruments for the near-real-time accounting system at the rokkasho Reprocessing Plant (RRP) of Japan Nuclear Fuel Limited (JNFL). The JNFL RRP is a large-scale commercial reprocessing facility for spent fuel from boiling-water and pressurized-water reactors. The facility comprises two major components: the main process area to separate and produce purified plutonium nitrate and uranyl nitrate from irradiated reactor spent fuels, and the co-denitration process area to combine and convert the plutonium nitrate and uranyl nitrate into mixed oxide (MOX). The selected NDA instruments for conceptual design studies are the MOX-product canister counter, holdup measurement systems for calcination and reduction furnaces and for blenders in the co-denitration process, the isotope dilution gamma-ray spectrometer for the spent fuel dissolver solution, and unattended verification systems. For more effective and practical safeguards and material control and accounting at RRP, the authors are also studying the conceptual design for the UO{sub 3} large-barrel counter. This paper discusses the state-of-the-art NDA conceptual design and research and development activities for the above instruments.

  20. Cold adaptation of the mononuclear molybdoenzyme periplasmic nitrate reductase from the Antarctic bacterium Shewanella gelidimarina

    SciTech Connect (OSTI)

    Simpson, Philippa J.L.; Codd, Rachel; School of Medical Sciences and Bosch Institute, University of New South Wales, New South Wales 2006

    2011-11-04

    Highlights: Black-Right-Pointing-Pointer Cold-adapted phenotype of NapA from the Antarctic bacterium Shewanella gelidimarina. Black-Right-Pointing-Pointer Protein homology model of NapA from S. gelidimarina and mesophilic homologue. Black-Right-Pointing-Pointer Six amino acid residues identified as lead candidates governing NapA cold adaptation. Black-Right-Pointing-Pointer Molecular-level understanding of designing cool-temperature in situ oxyanion sensors. -- Abstract: The reduction of nitrate to nitrite is catalysed in bacteria by periplasmic nitrate reductase (Nap) which describes a system of variable protein subunits encoded by the nap operon. Nitrate reduction occurs in the NapA subunit, which contains a bis-molybdopterin guanine dinucleotide (Mo-MGD) cofactor and one [4Fe-4S] iron-sulfur cluster. The activity of periplasmic nitrate reductase (Nap) isolated as native protein from the cold-adapted (psychrophilic) Antarctic bacterium Shewanella gelidimarina (Nap{sub Sgel}) and middle-temperature adapted (mesophilic) Shewanella putrefaciens (Nap{sub Sput}) was examined at varied temperature. Irreversible deactivation of Nap{sub Sgel} and Nap{sub Sput} occurred at 54.5 and 65 Degree-Sign C, respectively. When Nap{sub Sgel} was preincubated at 21-70 Degree-Sign C for 30 min, the room-temperature nitrate reductase activity was maximal and invariant between 21 and 54 Degree-Sign C, which suggested that Nap{sub Sgel} was poised for optimal catalysis at modest temperatures and, unlike Nap{sub Sput}, did not benefit from thermally-induced refolding. At 20 Degree-Sign C, Nap{sub Sgel} reduced selenate at 16% of the rate of nitrate reduction. Nap{sub Sput} did not reduce selenate. Sequence alignment showed 46 amino acid residue substitutions in Nap{sub Sgel} that were conserved in NapA from mesophilic Shewanella, Rhodobacter and Escherichia species and could be associated with the Nap{sub Sgel} cold-adapted phenotype. Protein homology modeling of Nap{sub Sgel} using a mesophilic template with 66% amino acid identity showed the majority of substitutions occurred at the protein surface distal to the Mo-MGD cofactor. Two mesophilic {r_reversible} psychrophilic substitutions (Asn {r_reversible} His, Val {r_reversible} Trp) occurred in a region close to the surface of the NapA substrate funnel resulting in potential interdomain {pi}-{pi} and/or cation-{pi} interactions. Three mesophilic {r_reversible} psychrophilic substitutions occurred within 4.5 A of the Mo-MGD cofactor (Phe {r_reversible} Met, Ala {r_reversible} Ser, Ser {r_reversible} Thr) resulting in local regions that varied in hydrophobicity and hydrogen bonding networks. These results contribute to the understanding of thermal protein adaptation in a redox-active mononuclear molybdenum enzyme and have implications in optimizing the design of low-temperature environmental biosensors.

  1. Comparison of FTIR and Particle Mass Spectrometry for the Measurement of Paticulate Organic Nitrates

    SciTech Connect (OSTI)

    Bruns, Emily; Perraud, Veronique; Zelenyuk, Alla; Ezell, Michael J.; Johnson, Stanley N.; Yu, Yong; Imre, D.; Finlayson-Pitts, Barbara J.; Alexander, M. L.

    2010-02-01

    While multifunctional organic nitrates are formed during the atmospheric oxidation of volatile organic compounds, relatively little is known about their signatures in particle mass spectrometers. High resolution time-of-flight aerosol mass spectrometry (HR-ToF-AMS) was applied to NH4NO3, NaNO3 and isosorbide 5-mononitrate (IMN) particles, and to secondary organic aerosol (SOA) from NO3 radical reactions at 22 C and 1 atm in air with and pinene, 3-carene, limonene and isoprene. For comparison, single particle laser ablation mass spectra (SPLAT II) were also obtained for IMN and SOA from the pinene reaction. The mass spectra of all particles exhibit significant intensity at m/z 30, and for the SOA, weak peaks corresponding to various organic fragments containing nitrogen [CxHyNzOa]+ were identified using HR-ToF-AMS. The NO+/NO2+ ratios from HR-ToF-AMS were 10-15 for IMN and the SOA from the and pinene, 3-carene and limonene reactions, ~5 for the isoprene reaction, 2.4 for NH4NO3 and 80 for NaNO3. The N/H ratios from HR-ToF-AMS for the SOA were smaller by a factor of 2 to 4 than the -ONO2/C-H ratios measured using FTIR on particles impacted on ZnSe windows. While the NO+/NO2+ ratio may provide a generic indication of organic nitrates under some conditions, specific identification of particulate organic nitrates awaits further development of particle mass spectrometry techniques.

  2. Dirac solutions for quaternionic potentials

    SciTech Connect (OSTI)

    De Leo, Stefano Giardino, Sergio

    2014-02-15

    The Dirac equation is solved for quaternionic potentials, i?V{sub 0} + j?W{sub 0} (V{sub 0}?R , W{sub 0}?C). The study shows two different solutions. The first one contains particle and anti-particle solutions and leads to the diffusion, tunneling, and Klein energy zones. The standard solution is recovered taking the complex limit of this solution. The second solution, which does not have a complex counterpart, can be seen as a V{sub 0}-antiparticle or |W{sub 0}|-particle solution.

  3. Process for converting sodium nitrate-containing, caustic liquid radioactive wastes to solid insoluble products

    DOE Patents [OSTI]

    Barney, Gary S.; Brownell, Lloyd E.

    1977-01-01

    A method for converting sodium nitrate-containing, caustic, radioactive wastes to a solid, relatively insoluble, thermally stable form is provided and comprises the steps of reacting powdered aluminum silicate clay, e.g., kaolin, bentonite, dickite, halloysite, pyrophyllite, etc., with the sodium nitrate-containing radioactive wastes which have a caustic concentration of about 3 to 7 M at a temperature of 30.degree. C to 100.degree. C to thereby entrap the dissolved radioactive salts in the aluminosilicate matrix. In one embodiment the sodium nitrate-containing, caustic, radioactive liquid waste, such as neutralized Purex-type waste, or salts or oxide produced by evaporation or calcination of these liquid wastes (e.g., anhydrous salt cake) is converted at a temperature within the range of 30.degree. C to 100.degree. C to the solid mineral form-cancrinite having an approximate chemical formula 2(NaAlSiO.sub.4) .sup.. xSalt.sup.. y H.sub.2 O with x = 0.52 and y = 0.68 when the entrapped salt is NaNO.sub.3. In another embodiment the sodium nitrate-containing, caustic, radioactive liquid is reacted with the powdered aluminum silicate clay at a temperature within the range of 30.degree. C to 100.degree. C, the resulting reaction product is air dried eitheras loose powder or molded shapes (e.g., bricks) and then fired at a temperature of at least 600.degree. C to form the solid mineral form-nepheline which has the approximate chemical formula of NaAlSiO.sub.4. The leach rate of the entrapped radioactive salts with distilled water is reduced essentially to that of the aluminosilicate lattice which is very low, e.g., in the range of 10.sup.-.sup.2 to 10.sup.-.sup.4 g/cm.sup.2 -- day for cancrinite and 10.sup.-.sup.3 to 10.sup.-.sup.5 g/cm.sup.2 -- day for nepheline.

  4. Sandia Energy - SCADA Engineering Solutions

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

    Engineering Solutions Home Stationary Power Safety, Security & Resilience of Energy Infrastructure Grid Modernization Cyber Security for Electric Infrastructure National...

  5. Options Assessment Report: Treatment of Nitrate Salt Waste at Los Alamos National Laboratory

    SciTech Connect (OSTI)

    Robinson, Bruce Alan; Stevens, Patrice Ann

    2015-12-17

    This report documents the methodology used to select a method of treatment for the remediated nitrate salt (RNS) and unremediated nitrate salt (UNS) waste containers at Los Alamos National Laboratory (LANL). The method selected should treat the containerized waste in a manner that renders the waste safe and suitable for transport and final disposal in the Waste Isolation Pilot Plant (WIPP) repository, under specifications listed in the WIPP Waste Acceptance Criteria (DOE/CBFO, 2013). LANL recognizes that the results must be thoroughly vetted with the New Mexico Environment Department (NMED) and that a modification to the LANL Hazardous Waste Facility Permit is a necessary step before implementation of this or any treatment option. Likewise, facility readiness and safety basis approvals must be received from the Department of Energy (DOE). This report presents LANL’s preferred option, and the documentation of the process for reaching the recommended treatment option for RNS and UNS waste, and is presented for consideration by NMED and DOE.

  6. A study of the organic emission from a turbocharged diesel engine running on 12 percent hexyl nitrate dissolved in ethanol

    SciTech Connect (OSTI)

    Walde, N.; Westerholm, R.; Persson, K.-A.

    1984-01-01

    A highly rated turbocharged diesel engine adapted for an alternative fuel based on ethanol and hexyl nitrate has been investigated with respect to the emission of organic compounds in the exhausts. The adaption involves: ignition nozzles with larger holes, a change of injection timing and more fuel injected per stroke. Emissions were measured at four different driving modes ie, 1, 8, 10 and 12 respectively, in the California Cycle. The exhaust composition are different compared to conventional diesel emissions. The main part of the organic pollutants consists of unburned ethanol and hexyl nitrate, acetaldehyde being the most abundant aldehyde.

  7. Suntech Energy Solutions Formerly EI Solutions | Open Energy...

    Open Energy Info (EERE)

    Place: Pasadena, California Zip: 91103 Sector: Solar Product: A California-based solar power systems integrator and installer. References: Suntech Energy Solutions...

  8. Evaluation of the Magnesium Hydroxide Treatment Process for Stabilizing PFP Plutonium/Nitric Acid Solutions

    SciTech Connect (OSTI)

    Gerber, Mark A.; Schmidt, Andrew J.; Delegard, Calvin H.; Silvers, Kurt L.; Baker, Aaron B.; Gano, Susan R.; Thornton, Brenda M.

    2000-09-28

    This document summarizes an evaluation of the magnesium hydroxide [Mg(OH)2] process to be used at the Hanford Plutonium Finishing Plant (PFP) for stabilizing plutonium/nitric acid solutions to meet the goal of stabilizing the plutonium in an oxide form suitable for storage under DOE-STD-3013-99. During the treatment process, nitric acid solutions bearing plutonium nitrate are neutralized with Mg(OH)2 in an air sparge reactor. The resulting slurry, containing plutonium hydroxide, is filtered and calcined. The process evaluation included a literature review and extensive laboratory- and bench-scale testing. The testing was conducted using cerium as a surrogate for plutonium to identify and quantify the effects of key processing variables on processing time (primarily neutralization and filtration time) and calcined product properties.

  9. Better Buildings Residential Program Solution Center Demonstration |

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

    Department of Energy Residential Program Solution Center Demonstration Better Buildings Residential Program Solution Center Demonstration Better Buildings Residential Program Solution Center Demonstration from the U.S. Department of Energy. PDF icon Solution Center Demo More Documents & Publications Building Science Solutions … Faster and Better Presentation: Better Buildings Residential Program Solution Center Presentation: Better Buildings Residential Program Solution Center

  10. Financing Solutions | Department of Energy

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

    Financing Solutions Financing Solutions Transitioning to a clean energy economy requires innovative financing solutions that enable state, local, and tribal governments to invest in clean energy technologies. However, the clean energy puzzle can be daunting, especially when it comes to financing. With that in mind this website aims to provide an overview of financing as it pertains to state, local, and tribal governments who are designing and implementing clean energy financing programs. Learn

  11. Structural Aspects of Hydrogen Bonding with Nitrate and Sulfate: Design Criteria for Polyalcohol Hosts

    SciTech Connect (OSTI)

    Hay, Benjamin P.; Dixon, David A.; Lumetta, Gregg J.; Vargas, Rubicelia; Garza, Jorge

    2004-01-01

    Organic hosts for oxyanion complexation can be constructed by combining two or more hydrogen bonding sites. The deliberate design of architectures for such hosts requires knowledge of the optimal geometry for the hydrogen bonds formed between the host and the guest. Important structural parameters include the O--H distance, the O--H-D angle, the X-O--H angle, and the X-O--H-D dihedral angle (H-D=hydrogen bond donor, X=any atom). This information can be obtained through the analysis of hydrogen bonding observed in crystal structures and electronic structure calculations on simple gas-phase complexes. In this chapter, we present an analysis of hydrogen bonding structural parameters for alcohol hydrogen donors and the oxygen atom acceptors in nitrate and sulfate.

  12. Thermal behavior of glassy phase stabilized ammonium nitrate (PSAN) thin films

    SciTech Connect (OSTI)

    Yeager, J. D.; Chellappa, R.; Singh, S.; Majewski, J.

    2015-06-01

    Ammonium nitrate (AN) is a high interest material because of its wide usage in propellants and explosives but can be difficult to handle from a formulation standpoint. It is soluble in many common solvents and has complex phase behavior. Here, we formulate phase stabilized AN (PSAN) films in a polymer matrix and characterize thermal and phase behavior using neutron reflectometry and ellipsometry. Our PSAN films are generally stable up to 160 C, though we observe small material loss between 60 and 100 C, which we attribute to solvent interactions with the PSAN. Crystallization of AN from supersaturated polymer is most common at thicker regions of the film, suggesting a critical nucleation thickness for the AN which can be avoided by making very thin films.

  13. Thermal behavior of glassy phase stabilized ammonium nitrate (PSAN) thin films

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Yeager, J. D.; Chellappa, R.; Singh, S.; Majewski, J.

    2015-06-01

    Ammonium nitrate (AN) is a high interest material because of its wide usage in propellants and explosives but can be difficult to handle from a formulation standpoint. It is soluble in many common solvents and has complex phase behavior. Here, we formulate phase stabilized AN (PSAN) films in a polymer matrix and characterize thermal and phase behavior using neutron reflectometry and ellipsometry. Our PSAN films are generally stable up to 160 °C, though we observe small material loss between 60 and 100 °C, which we attribute to solvent interactions with the PSAN. Crystallization of AN from supersaturated polymer is mostmore » common at thicker regions of the film, suggesting a critical nucleation thickness for the AN which can be avoided by making very thin films.« less

  14. Extraordinary vacuum black string solutions

    SciTech Connect (OSTI)

    Kim, Hyeong-Chan; Lee, Jungjai

    2008-01-15

    In addition to the boosted static solution there are two other classes of stationary stringlike solutions of the vacuum Einstein equation in (4+1) dimensions. Each class is characterized by three parameters of mass, tension, and momentum flow along the fifth coordinate. We analyze the metric properties of one of the two classes, which was previously assumed to be naked singular, and show that the solution spectrum contains black string and wormhole in addition to the known naked singularity as the momentum flow to mass ratio increases. Interestingly, there does not exist new zero momentum solution in these cases.

  15. Biofuel Solutions | Open Energy Information

    Open Energy Info (EERE)

    developer, which had been developing one plant in Fairmont, Minnesota and another in Wood River, Biofuel Energy LLC took over plant development of Biofuel Solutions' projects in...

  16. MPower Solutions | Open Energy Information

    Open Energy Info (EERE)

    Dundee,, United Kingdom Zip: DD2 4UH Product: MPower Solutions is one Europe's largest battery manufacturers supplying over 500,000 batteries every month. MPower provides optimised...

  17. Employment Solutions Division (HC-13)

    Broader source: Energy.gov [DOE]

    This division develops and implements innovative HCM business solutions relating to corporate recruiting, organizational and workforce development, workforce and succession planning, talent...

  18. SBY Solutions | Open Energy Information

    Open Energy Info (EERE)

    Jump to: navigation, search Name: SBY Solutions Place: Israel Zip: 42836 Sector: Solar Product: Solar panel installer, mainly focusing on rooftops. References: SBY...

  19. Extracting alcohols from aqueous solutions

    DOE Patents [OSTI]

    Compere, Alicia L.; Googin, John M.; Griffith, William L.

    1984-01-01

    Hydrocarbon and surfactants are contacted with a solution of alcohol and water to extract the alcohol into the hydrocarbon-surfactant mixture.

  20. DEVELOPMENT Solutions | Open Energy Information

    Open Energy Info (EERE)

    Product: DEVELOPMENT Solutions (DS) supports investors to realise projects with sustainable applications, including in the areas of environment, energy efficiency, water...

  1. Cleantech Solutions | Open Energy Information

    Open Energy Info (EERE)

    New York Zip: 10023 Region: Northeast - NY NJ CT PA Area Sector: Efficiency Product: Energy efficiency solutions and consumption monitoring systems for buildings Website:...

  2. RWE Solutions | Open Energy Information

    Open Energy Info (EERE)

    RWE Solutions Place: Neu-Isenburg, Germany Zip: 63263 Sector: Solar Product: Germany-based, subsidiary of RWE AG plans, builds and manages energy infrastructure for utilities...

  3. High conductivity electrolyte solutions and rechargeable cells incorporating such solutions

    DOE Patents [OSTI]

    Angell, Charles Austen (Mesa, AZ); Zhang, Sheng-Shui (Tucson, AZ); Xu, Kang (Tempe, AZ)

    1998-01-01

    This invention relates generally to electrolyte solvents for use in liquid or rubbery polymer electrolyte solutions as are used, for example, in electrochemical devices. More specifically, this invention relates to sulfonyl/phospho-compound electrolyte solvents and sulfonyl/phospho-compound electrolyte solutions incorporating such solvents.

  4. High conductivity electrolyte solutions and rechargeable cells incorporating such solutions

    DOE Patents [OSTI]

    Angell, C.A.; Zhang, S.S.; Xu, K.

    1998-10-20

    This invention relates generally to electrolyte solvents for use in liquid or rubbery polymer electrolyte solutions as are used, for example, in electrochemical devices. More specifically, this invention relates to sulfonyl/phospho-compound electrolyte solvents and sulfonyl/phospho-compound electrolyte solutions incorporating such solvents. 9 figs.

  5. Dow Building Solutions | Open Energy Information

    Open Energy Info (EERE)

    Dow Building Solutions Jump to: navigation, search Name: Dow Building Solutions Place: Midland, MI Website: www.dowbuildingsolutions.com References: Dow Building Solutions1...

  6. Future Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    Solutions Jump to: navigation, search Name: Future Energy Solutions Place: Didcot, United Kingdom Zip: OX11 0QR Product: Future Energy Solutions is a sustainable energy...

  7. Carbon Solutions Group | Open Energy Information

    Open Energy Info (EERE)

    Solutions Group Jump to: navigation, search Name: Carbon Solutions Group Place: Chicago, Illinois Zip: 60601 Sector: Carbon Product: Carbon Solutions Group collaborates with...

  8. Solar Choice Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Choice Solutions Inc Jump to: navigation, search Name: Solar Choice Solutions Inc. Place: Calabasas, California Zip: 91302 Sector: Solar Product: Solar Choice Solutions Inc. is an...

  9. Mechanical Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Mechanical Solutions Inc Jump to: navigation, search Name: Mechanical Solutions Inc Place: New York Product: New York-based contractor. References: Mechanical Solutions Inc1 This...

  10. Chevron Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    Chevron Energy Solutions Jump to: navigation, search Logo: Chevron Energy Solutions Name: Chevron Energy Solutions Address: 345 California Street, 18th Floor Place: San Francisco,...

  11. Wind Park Solutions Arcadia | Open Energy Information

    Open Energy Info (EERE)

    Park Solutions Arcadia Jump to: navigation, search Name: Wind Park Solutions Arcadia Place: Big Sandy, Montana Sector: Wind energy Product: JV between Wind Park Solutions America...

  12. Institute for Environmental Solutions | Open Energy Information

    Open Energy Info (EERE)

    Environmental Solutions Jump to: navigation, search Logo: Institute for Environmental Solutions Name: Institute for Environmental Solutions Address: 761 Newport St. Place: Denver,...

  13. ECO Solutions LLC | Open Energy Information

    Open Energy Info (EERE)

    ECO Solutions LLC Jump to: navigation, search Name: ECO Solutions, LLC Place: Chatsworth, Georgia Zip: 30705 Product: ECO Solutions operates a biodiesel plant in Georgia with a...

  14. AFV Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Solutions Inc Place: Mesa, Arizona Zip: 85210 Product: AFV Solutions is a manufacturer of electric-hybrid buses and energy conversion systems for cars. References: AFV Solutions...

  15. Energy Capital Solutions | Open Energy Information

    Open Energy Info (EERE)

    Capital Solutions Jump to: navigation, search Logo: Energy Capital Solutions Name: Energy Capital Solutions Address: 2651 North Harwood Street, Suite 410 Place: Dallas, Texas Zip:...

  16. THE SENSITIVITY OF CARBON STEELS' SUSCEPTIBILITY TO LOCALIZED CORROSION TO THE PH OF NITRATE BASED NUCLEAR WASTES

    SciTech Connect (OSTI)

    BOOMER KD

    2010-01-14

    The Hanford tank reservation contains approximately 50 million gallons of liquid legacy radioactive waste from cold war weapons production, which is stored in 177 underground storage tanks. The tanks will be in use until waste processing operations are completed. The wastes tend to be high pH (over 10) and nitrate based. Under these alkaline conditions carbon steels tend to be passive and undergo relatively slow uniform corrosion. However, the presence of nitrate and other aggressive species, can lead to pitting and stress corrosion cracking. This work is a continuation of previous work that investigated the propensity of steels to suffer pitting and stress corrosion cracking in various waste simulants. The focus of this work is an investigation of the sensitivity of the steels' pitting and stress corrosion cracking susceptibility tosimulant pH. Previous work demonstrated that wastes that are high in aggressive nitrate and low in inhibitory nitrite are susceptible to localized corrosion. However, the previous work involved wastes with pH 12 or higher. The current work involves wastes with lower pH of 10 or 11. It is expected that at these lower pHs that a higher nitrite-to-nitrate ratio will be necessary to ensure tank integrity. This experimental work involved both electrochemical testing, and slow strain rate testing at either the free corrosion potential or under anodic polarization. The results of the current work will be discussed, and compared to work previously presented.

  17. Draft Genome Sequence for Microbacterium laevaniformans Strain OR221, a Bacterium Tolerant to Metals, Nitrate, and Low pH

    SciTech Connect (OSTI)

    Brown, Steven D; Palumbo, Anthony Vito; Panikov, Nikolai; Ariyawansa, Thilini; Klingeman, Dawn Marie; Johnson, Courtney M; Land, Miriam L; Utturkar, Sagar M; Epstein, Slava

    2012-01-01

    Microbacterium laevaniformans strain OR221 was isolated from subsurface sediments obtained from the Field Research Center (FRC) in Oak Ridge, TN. It was characterized as a bacterium tolerant to heavy metals such as uranium, nickel, cobalt, cadmium, as well as nitrate and low pH. We present its draft genome sequence.

  18. BROADER National Security Missions

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

    Metal Chips (U) Uranium Trioxide (UO 3 ) UO 2 (NO 3 ) 2 Ur anyl Nitrate Ammonium Uranyl Carbonate (NH 4 ) 2 UO 2 (CO 3 ) 4 DEVELOP NEW NATIONAL SECURITY MISSIONS Y-12 has...

  19. Iron-stabilized nanocrystalline ZrO{sub 2} solid solutions: Synthesis by combustion and thermal stability

    SciTech Connect (OSTI)

    Legorreta Garcia, Felipe; Resende, Valdirene Gonzaga de; De Grave, Eddy; Peigney, Alain; Barnabe, Antoine; Laurent, Christophe

    2009-06-03

    The synthesis of Fe{sup 3+}-stabilized zirconia by the nitrate/urea combustion route was investigated. Using several characterization techniques, including X-ray diffraction, field-emission-gun scanning electron microscopy and notably Moessbauer spectroscopy, it was possible to determine the appropriate amount of urea that allows to obtain a totally stabilized Zr{sub 0.9}Fe{sub 0.1}O{sub 1.95} solid solution. The nanocrystalline zirconia solid solution is mostly tetragonal, but the presence of the cubic phase could not be ruled out. An in-depth study of the thermal stability in air showed that the Fe{sup 3+} solubility in the stabilized solid solution starts to decrease at about 875 deg. C which results in the formation of hematite (possibly containing some Zr{sup 4+}) at the surface of the zirconia grains and further provokes the progressive transformation into the monoclinic zirconia phase.

  20. Uranium Fate in Hanford Sediment Altered by Simulated Acid Waste Solutions

    SciTech Connect (OSTI)

    Gartman, Brandy N.; Qafoku, Nikolla; Szecsody, James E.; Kukkadapu, Ravi K.; Wang, Zheming; Wellman, Dawn M.; Truex, Michael J.

    2015-07-24

    Many aspects of U(VI) behavior in sediments that are previously exposed to acidic waste fluids for sufficiently long times to induce significant changes in pH and other physical, mineralogical and chemical properties, are not well documented in the literature. For this reason, we conducted a series of macroscopic batch experiments combined with a variety of bulk characterization studies (Mssbauer and laser spectroscopy), micro-scale inspections (-XRF), and molecular scale interrogations (XANES) with the objectives to: i) determine the extent of U(VI) partitioning to Hanford sediments previously exposed to acidic waste simulants (pH = 2 and pH = 5) and under neutral conditions (pH = 8) at varying background solution concentrations (i.e., NaNO3); ii) determine micron-scale solid phase associated U valence state and phase identity; and iii) provide information for a plausible conceptual model of U(VI) attenuation under waste plume acidic conditions. The results of the batch experiments showed that the acid pre-treated sediment had high affinity for aqueous U(VI), which was removed from solution via two pH dependent and apparently different mechanisms (adsorption at pH = 2 and precipitation at pH = 5). The micro-scale inspections and XANES analyses confirmed that high concentration areas were rich mainly in U(VI), demonstrating that most of the added U(VI) was not reduced to U(IV). The laser spectroscopy data showed that uranyl phosphates {e.g. metaautunite [Ca(UO2)2(PO4)210-12H2O] and phosphuranylite [KCa(H3O)3(UO2)7(PO4)4O48(H2O)]} were present in the sediments. They also showed clear differences between the U bearing phases in the experiments conducted in the presence or absence of air. The data generated from these experiments will help in a better understanding of the reactions and processes that have a significant effect and/or control U mobility.

  1. Performance testing accountability measurements

    SciTech Connect (OSTI)

    Oldham, R.D.; Mitchell, W.G.; Spaletto, M.I.

    1993-12-31

    The New Brunswick Laboratory (NBL) provides assessment support to the DOE Operations Offices in the area of Material Control and Accountability (MC and A). During surveys of facilities, the Operations Offices have begun to request from NBL either assistance in providing materials for performance testing of accountability measurements or both materials and personnel to do performance testing. To meet these needs, NBL has developed measurement and measurement control performance test procedures and materials. The present NBL repertoire of performance tests include the following: (1) mass measurement performance testing procedures using calibrated and traceable test weights, (2) uranium elemental concentration (assay) measurement performance tests which use ampulated solutions of normal uranyl nitrate containing approximately 7 milligrams of uranium per gram of solution, and (3) uranium isotopic measurement performance tests which use ampulated uranyl nitrate solutions with enrichments ranging from 4% to 90% U-235. The preparation, characterization, and packaging of the uranium isotopic and assay performance test materials were done in cooperation with the NBL Safeguards Measurements Evaluation Program since these materials can be used for both purposes.

  2. Fernald Environmental Management Project Director's Final Findings & Orders, December 27, 1994 Summary

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

    CERCLA Scope Summary Establish guidelines and deadlines for neutralization/removal of the hazardous waste in the uranyl nitrate hexahydrate (UNH) System Parties DOE; Fernald Environmental Restoration Management Corporation (FERMCO); Ohio Environmental Protection Agency Date 12/27/1994 SCOPE * Establish guidelines and deadlines for neutralization/removal of the hazardous waste in the uranyl nitrate hexahydrate (UNH) System. ESTABLISHING MILESTONES * Deadlines for completing certain activities

  3. Precipitation pathways for ferrihydrite formation in acidic solutions

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Zhu, Mengqiang; Khalid, Syed; Frandsen, Cathrine; Wallace, Adam F.; Legg, Benjamin; Zhang, Hengzhong; Morup, Steen; Banfield, Jillian F.; Waychunas, Glenn A.

    2015-10-03

    In this study, iron oxides and oxyhydroxides form via Fe3+ hydrolysis and polymerization in many aqueous environments, but the pathway from Fe3+ monomers to oligomers and then to solid phase nuclei is unknown. In this work, using combined X-ray, UV–vis, and Mössbauer spectroscopic approaches, we were able to identify and quantify the long-time sought ferric speciation over time during ferric oxyhydroxide formation in partially-neutralized ferric nitrate solutions ([Fe3+] = 0.2 M, 1.8 < pH < 3). Results demonstrate that Fe exists mainly as Fe(H2O)63+, μ-oxo aquo dimers and ferrihydrite, and that with time, the μ-oxo dimer decreases while the othermore » two species increase in their concentrations. No larger Fe oligomers were detected. Given that the structure of the μ-oxo dimer is incompatible with those of all Fe oxides and oxyhydroxides, our results suggest that reconfiguration of the μ-oxo dimer structure occurs prior to further condensation leading up to the nucleation of ferrihydrite. The structural reconfiguration is likely the rate-limiting step involved in the nucleation process.« less

  4. CRITICALITY SAFETY OF PROCESSING SALT SOLUTION AT SRS

    SciTech Connect (OSTI)

    Stephens, K; Davoud Eghbali, D; Michelle Abney, M

    2008-01-15

    High level radioactive liquid waste generated as a result of the production of nuclear material for the United States defense program at the Savannah River Site has been stored as 36 million gallons in underground tanks. About ten percent of the waste volume is sludge, composed of insoluble metal hydroxides primarily hydroxides of Mn, Fe, Al, Hg, and most radionuclides including fission products. The remaining ninety percent of the waste volume is saltcake, composed of primarily sodium (nitrites, nitrates, and aluminates) and hydroxides. Saltcakes account for 30% of the radioactivity while the sludge accounts for 70% of the radioactivity. A pilot plant salt disposition processing system has been designed at the Savannah River Site for interim processing of salt solution and is composed of two facilities: the Actinide Removal Process Facility (ARPF) and the Modular Caustic Side Solvent Extraction Unit (MCU). Data from the pilot plant salt processing system will be used for future processing salt at a much higher rate in a new salt processing facility. Saltcake contains significant amounts of actinides, and other long-lived radioactive nuclides such as strontium and cesium that must be extracted prior to disposal as low level waste. The extracted radioactive nuclides will be mixed with the sludge from waste tanks and vitrified in another facility. Because of the presence of highly enriched uranium in the saltcake, there is a criticality concern associated with concentration and/or accumulation of fissionable material in the ARP and MCU.

  5. Sunflower Solutions | Open Energy Information

    Open Energy Info (EERE)

    tracking systems maker for PV modules targeted at installations in the developing world. References: Sunflower Solutions1 This article is a stub. You can help OpenEI by...

  6. Cold Climate Building Enclosure Solutions

    Office of Scientific and Technical Information (OSTI)

    Enclosure Solutions Jan Kosny, Ali Fallahi, and Nitin Shukla Fraunhofer CSE January 2013 NOTICE This report was prepared as an account of work sponsored by an agency of the...

  7. Comprehensive Water-Efficiency Solutions

    SciTech Connect (OSTI)

    McMordie Stoughton, Kate

    2015-07-15

    Energy performance contracts can be an effective way to integrate comprehensive water-efficient technologies and solutions into energy efficiency projects. Current practices often miss key opportunities to incorporate a full suite of water measures primarily because a comprehensive approach is not taken in the assessment. This article provides information on how to develop a comprehensive water project that leads to innovative solutions and potential for large water reduction.

  8. Cosmological solution moduli of bigravity

    SciTech Connect (OSTI)

    Yılmaz, Nejat Tevfik

    2015-09-29

    We construct the complete set of metric-configuration solutions of the ghost-free massive bigravity for the scenario in which the g−metric is the Friedmann-Lemaitre-Robertson-Walker (FLRW) one, and the interaction Lagrangian between the two metrics contributes an effective ideal fluid energy-momentum tensor to the g-metric equations. This set corresponds to the exact background cosmological solution space of the theory.

  9. New Solutions Require New Thinking

    Office of Environmental Management (EM)

    Solutions Require New Thinking America's demand for power threatens to overburden an already congested electric system. The U.S. Department of Energy is addressing these energy challenges with innovative solutions to energy generation. Its Renewable and Distributed Systems Integration (RDSI) Program is helping to alleviate congestion, reduce greenhouse gas emissions, and improve reliability by investigating answers such as * Microgrid technologies * Distributed generation * Two-way communication

  10. Isotopic identification of soil and permafrost nitrate sources in an Arctic tundra ecosystem

    SciTech Connect (OSTI)

    Heikoop, Jeffrey M.; Throckmorton, Heather M.; Newman, Brent D.; Perkins, George B.; Iversen, Colleen M.; Chowdhury, Taniya Roy; Romanovsky, Vladimir E.; Graham, David E.; Norby, Richard J.; Wilson, Cathy J.; Wullschleger, Stan D.

    2015-06-08

    The nitrate (NO??) dual isotope approach was applied to snowmelt, tundra active layer pore waters, and underlying permafrost in Barrow, Alaska, USA, to distinguish between NO?? derived from at NO?? signal with ??N averaging 4.8 1.0 (standard error of the mean) and ??O averaging 70.2 1.7. In active layer pore waters, NO?? primarily occurred at concentrations suitable for isotopic analysis in the relatively dry and oxic centers of high-centered polygons. The average ??N and ??O of NO?? from high-centered polygons were 0.5 1.1 and 4.1 0.6, respectively. When compared to the ??N of reduced nitrogen (N) sources, and the ??O of soil pore waters, it was evident that NO?? in high-centered polygons was primarily from microbial nitrification. Permafrost NO?? had ??N ranging from approximately 6 to 10, similar to atmospheric and microbial NO??, and highly variable ??O ranging from approximately 2 to 38. Permafrost ice wedges contained a significant atmospheric component of NO??, while permafrost textural ice contained a greater proportion of microbially derived NO??. Large-scale permafrost thaw in this environment would release NO?? with a ??O signature intermediate to that of atmospheric and microbial NO?. Consequently, while atmospheric and microbial sources can be readily distinguished by the NO?? dual isotope technique in tundra environments, attribution of NO?? from thawing permafrost will not be straightforward. The NO?? isotopic signature, however, appears useful in identifying NO?? sources in extant permafrost ice.

  11. Materials corrosion of high temperature alloys immersed in 600C binary nitrate salt.

    SciTech Connect (OSTI)

    Kruizenga, Alan Michael; Gill, David Dennis; LaFord, Marianne Elizabeth

    2013-03-01

    Thirteen high temperature alloys were immersion tested in a 60/40 binary nitrate salt. Samples were interval tested up to 3000 hours at 600%C2%B0C with air as the ullage gas. Chemical analysis of the molten salt indicated lower nitrite concentrations present in the salt, as predicted by the equilibrium equation. Corrosion rates were generally low for all alloys. Corrosion products were identified using x-ray diffraction and electron microprobe analysis. Fe-Cr based alloys tended to form mixtures of sodium and iron oxides, while Fe-Ni/Cr alloys had similar corrosion products plus oxides of nickel and chromium. Nickel based alloys primarily formed NiO, with chromium oxides near the oxide/base alloy interface. In625 exhibited similar corrosion performance in relation to previous tests, lending confidence in comparisons between past and present experiments. HA230 exhibited internal oxidation that consisted of a nickel/chromium oxide. Alloys with significant aluminum alloying tended to exhibit superior performance, due formation of a thin alumina layer. Soluble corrosion products of chromium, molybdenum, and tungsten were also formed and are thought to be a significant factor in alloy performance.

  12. Solidification of Acidic, High Nitrate Nuclear Wastes by Grouting or Absorption on Silica Gel

    SciTech Connect (OSTI)

    A. K. Herbst; S. V. Raman; R. J. Kirkham

    2004-01-01

    The use of grout and silica gel were explored for the solidification of four types of acidic, high nitrate radioactive wastes. Two methods of grouting were tested: direct grouting and pre-neutralization. Two methods of absorption on silica gel were also tested: direct absorption and rotary spray drying. The waste simulant acidity varied between 1 N and 12 N. The waste simulant was neutralized by pre-blending calcium hydroxide with Portland cement and blast furnace slag powders prior to mixing with the simulant for grout solidification. Liquid sodium hydroxide was used to partially neutralize the simulant to a pH above 2 and then it was absorbed for silica gel solidification. Formulations for each of these methods are presented along with waste form characteristics and properties. Compositional variation maps for grout formulations are presented which help determine the optimum "recipe" for a particular waste stream. These maps provide a method to determine the proportions of waste, calcium hydroxide, Portland cement, and blast furnace slag that provide a waste form that meets the disposal acceptance criteria. The maps guide researchers in selecting areas to study and provide an operational envelop that produces acceptable waste forms. The grouts both solidify and stabilize the wastes, while absorption on silica gel produces a solid waste that will not pass standard leaching procedures (TCLP) if required. Silica gel wastes can be made to pass most leach tests if heated to 600C.

  13. Polyethylene encapsulatin of nitrate salt wastes: Waste form stability, process scale-up, and economics

    SciTech Connect (OSTI)

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

    1991-07-01

    A polyethylene encapsulation system for treatment of low-level radioactive, hazardous, and mixed wastes has been developed at Brookhaven National Laboratory. Polyethylene has several advantages compared with conventional solidification/stabilization materials such as hydraulic cements. Waste can be encapsulated with greater efficiency and with better waste form performance than is possible with hydraulic cement. The properties of polyethylene relevant to its long-term durability in storage and disposal environments are reviewed. Response to specific potential failure mechanisms including biodegradation, radiation, chemical attack, flammability, environmental stress cracking, and photodegradation are examined. These data are supported by results from extensive waste form performance testing including compressive yield strength, water immersion, thermal cycling, leachability of radioactive and hazardous species, irradiation, biodegradation, and flammability. The bench-scale process has been successfully tested for application with a number of specific problem'' waste streams. Quality assurance and performance testing of the resulting waste form confirmed scale-up feasibility. Use of this system at Rocky Flats Plant can result in over 70% fewer drums processed and shipped for disposal, compared with optimal cement formulations. Based on the current Rocky Flats production of nitrate salt per year, polyethylene encapsulation can yield an estimated annual savings between $1.5 million and $2.7 million, compared with conventional hydraulic cement systems. 72 refs., 23 figs., 16 tabs.

  14. Mineral Dissolution and Secondary Precipitation on Quartz Sand in Simulated Hanford Tank Solutions Affecting Subsurface Porosity

    SciTech Connect (OSTI)

    Wang, Guohui; Um, Wooyong

    2012-11-23

    Highly alkaline nuclear waste solutions have been released from underground nuclear waste storage tanks and pipelines into the vadose zone at the U.S. Department of Energys Hanford Site in Washington, causing mineral dissolution and re-precipitation upon contact with subsurface sediments. High pH caustic NaNO3 solutions with and without dissolved Al were reacted with quartz sand through flow-through columns stepwise at 45, 51, and 89C to simulate possible reactions between leaked nuclear waste solution and primary subsurface mineral. Upon reaction, Si was released from the dissolution of quartz sand, and nitrate-cancrinite [Na8Si6Al6O24(NO3)2] precipitated on the quartz surface as a secondary mineral phase. Both steady-state dissolution and precipitation kinetics were quantified, and quartz dissolution apparent activation energy was determined. Mineral alteration through dissolution and precipitation processes results in pore volume and structure changes in the subsurface porous media. In this study, the column porosity increased up to 40.3% in the pure dissolution column when no dissolved Al was present in the leachate, whereas up to a 26.5% porosity decrease was found in columns where both dissolution and precipitation were observed because of the presence of Al in the input solution. The porosity change was also confirmed by calculation using the dissolution and precipitation rates and mineral volume changes.

  15. EP-AREAG-PLAN-1248, R.0 TA-54 Area G Nitrate-Salt Waste Container Response Instructions

    Office of Environmental Management (EM)

    EP-AREAG-PLAN-1248, R.0 TA-54 Area G Nitrate-Salt Waste Container Response Instructions Effective Date: 5/28/2014 The Responsible Manager has determined that the following organizations' review/concurrence is required for the initial document and for major revisions a same type and level review is required. Review documentation is contained in the Document History File: EWMO Engineering LANL TRU Programs - Shipping and Safe Storage Disposition LANL TRU Programs - Drum Disposition Project LANL

  16. Electrodialysis operation with buffer solution

    DOE Patents [OSTI]

    Hryn, John N. (Naperville, IL); Daniels, Edward J. (Orland Park, IL); Krumdick, Greg K. (Crete, IL)

    2009-12-15

    A new method for improving the efficiency of electrodialysis (ED) cells and stacks, in particular those used in chemical synthesis. The process entails adding a buffer solution to the stack for subsequent depletion in the stack during electrolysis. The buffer solution is regenerated continuously after depletion. This buffer process serves to control the hydrogen ion or hydroxide ion concentration so as to protect the active sites of electrodialysis membranes. The process enables electrodialysis processing options for products that are sensitive to pH changes.

  17. TrueWind Solutions | Open Energy Information

    Open Energy Info (EERE)

    TrueWind Solutions Jump to: navigation, search Name: TrueWind Solutions Place: Albany, NY Website: www.awstruepower.com References: TrueWind Solutions1 Information About...

  18. Recovery of uranium from dilute solution using liquid emulsion membrane system

    SciTech Connect (OSTI)

    Mukhopadhyay, S.; Ghosh, S.K.; Juvekar, V.A.

    2008-07-01

    The liquid emulsion membrane (LEM) technique has great potential for application in the nuclear industry for large interfacial area, low consumption of organics, and high recovery from dilute streams. A LEM system composed DEHPA-kerosene-SPAN80-HNO{sub 3} has been developed for recovery of uranium from dilute nitrate solution, which gives 98% extraction and 88% stripping in a single stage. An attempt has been made to understand the mechanism of the LEM process, in which phenomena like per-traction, occlusion, swelling, and leakage occur simultaneously. The effect of various parameters on these phenomena has been described with a mathematical model, which is able to explain the experimental findings. (authors)

  19. Exchange Reactions Between a Molten Salt and a Solution of Tri...

    Office of Scientific and Technical Information (OSTI)

    MERCURY COMPOUNDS; MINERAL ACIDS; MIXING; NICKEL; NICKEL COMPLEXES; NICKEL COMPOUNDS; NITRITES; NUMERICALS; OXALATES; POTASSIUM NITRATES; SEPARATION PROCESSES; SILICONES; SODIUM ...

  20. PowerIt Solutions | Open Energy Information

    Open Energy Info (EERE)

    Place: Seattle, Washington Zip: 98104 Product: Powerit Solutions provides energy demand response and demand control solutions for industrial and commercial applications....

  1. Blueprint for Sustainability - Sustainable Solutions for Every...

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

    Blueprint for Sustainability - Sustainable Solutions for Every Consumer Blueprint for Sustainability - Sustainable Solutions for Every Consumer Highlights of Ford's near, mid, and ...

  2. Reaction Engineering Solutions Ltd | Open Energy Information

    Open Energy Info (EERE)

    Ltd Jump to: navigation, search Name: Reaction Engineering Solutions Ltd. Place: Cambridge, United Kingdom Zip: CB4 3QG Product: PUk-based, provider of computational solutions...

  3. Bio Solutions Manufacturing Inc | Open Energy Information

    Open Energy Info (EERE)

    Solutions Manufacturing Inc Jump to: navigation, search Name: Bio Solutions Manufacturing Inc Place: Las Vegas, Nevada Zip: 89103 Product: Waste-to-energy bioremediation developer....

  4. First Carbon Solutions | Open Energy Information

    Open Energy Info (EERE)

    Solutions Jump to: navigation, search Name: First Carbon Solutions Place: Bethesda, Maryland Product: To be completed... Coordinates: 40.020185, -81.073819 Show Map Loading...

  5. AG Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    navigation, search Name: AG Solutions Inc. Place: Gladstone, Michigan Product: 10Mgpy biodiesel producer in Gladstone, Michigan. References: AG Solutions Inc.1 This article is a...

  6. Biodiesel Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Solutions Inc Jump to: navigation, search Name: Biodiesel Solutions Inc Place: Sparks, Nevada Zip: 89431 Product: Designs and manufactures processing equipment and accessories to...

  7. Guardian Energy Management Solutions | Open Energy Information

    Open Energy Info (EERE)

    Guardian Energy Management Solutions Jump to: navigation, search Name: Guardian Energy Management Solutions Address: 753 Forest Street, Suite 110 Place: Marlborough, Massachusetts...

  8. Duke Energy Generation Services formerly Cinergy Solutions |...

    Open Energy Info (EERE)

    Generation Services formerly Cinergy Solutions Jump to: navigation, search Name: Duke Energy Generation Services (formerly Cinergy Solutions) Place: Cincinatti, Ohio Zip: 45202...

  9. Building America Technologies Solutions Case Study: Ventilation...

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

    Technologies Solutions Case Study: Ventilation System Effectiveness and Tested Indoor Air Quality Impacts Building America Technologies Solutions Case Study: Ventilation System ...

  10. Island Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    search Name: Island Energy Solutions Place: Kailua, Hawaii Zip: 96734 Product: Island Energy Solutions, Inc. is an electrical contracting company, based out of Kailua, Oahu,...

  11. Eco Alternative Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    Solutions Jump to: navigation, search Name: Eco Alternative Energy Solutions Place: Puerto Rico Product: Puerto Rico-based majority owner of joint venture Pevafersa America, which...

  12. Energy Options Solutions | Open Energy Information

    Open Energy Info (EERE)

    Energy Options & Solutions Place: Ann Arbor, Michigan Zip: 48103 Product: Michigan-based alternative energy consultant. References: Energy Options & Solutions1 This article is a...

  13. Technology Market Solutions | Open Energy Information

    Open Energy Info (EERE)

    Solutions Jump to: navigation, search Name: Technology & Market Solutions Place: Fairfax Station, Virginia Zip: 22039 Product: A consulting practice concentrating on technological,...

  14. Tribal Renewable Energy Solutions and Partnerships: Collaborating...

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

    Renewable Energy Solutions and Partnerships: Collaborating Through the Headwinds of Change Tribal Renewable Energy Solutions and Partnerships: Collaborating Through the Headwinds ...

  15. Clean Energy Solutions Center | Open Energy Information

    Open Energy Info (EERE)

    Center Jump to: navigation, search Logo: Clean Energy Solutions Center Name Clean Energy Solutions Center AgencyCompany Organization Clean Energy Ministerial Sector Energy Focus...

  16. Atlas Material Testing Solutions | Open Energy Information

    Open Energy Info (EERE)

    Atlas Material Testing Solutions Jump to: navigation, search Name: Atlas Material Testing Solutions Place: Chicago, IL Zip: 60613 Website: atlas-mts.com Coordinates: 41.9529209,...

  17. Conservation Resource Solutions | Open Energy Information

    Open Energy Info (EERE)

    Solutions Jump to: navigation, search Name: Conservation Resource Solutions Place: Cumming, Georgia Zip: 30040 Sector: Services Product: String representation "Conservation Re ......

  18. Global Power Solutions LLC | Open Energy Information

    Open Energy Info (EERE)

    Global Power Solutions LLC Jump to: navigation, search Name: Global Power Solutions LLC Place: Colorado Zip: CO 80401 Sector: Geothermal energy Product: String representation...

  19. Ebony Solutions UK | Open Energy Information

    Open Energy Info (EERE)

    Ebony Solutions UK Jump to: navigation, search Name: Ebony Solutions UK Place: Northwich, Cheshire, United Kingdom Zip: CW8 2SX Product: A UK biodiesel manufacturer. References:...

  20. Solar Electric Solutions LLC | Open Energy Information

    Open Energy Info (EERE)

    Electric Solutions LLC Jump to: navigation, search Name: Solar Electric Solutions, LLC Place: Woodland Hills, California Zip: 91364 Sector: Solar Product: California-based...

  1. Energy Solutions Co Ltd | Open Energy Information

    Open Energy Info (EERE)

    Energy Solutions Co Ltd Jump to: navigation, search Name: Energy Solutions Co Ltd Place: Seoul, Korea (Republic) Sector: Efficiency Product: A Korean builderengineering contractor...

  2. BFC Solutions Limited | Open Energy Information

    Open Energy Info (EERE)

    BFC Solutions Limited Jump to: navigation, search Name: BFC Solutions Limited Place: Taunton, England, United Kingdom Zip: TA1 PEJ Sector: Carbon Product: Somerset-based...

  3. PNE Renewable Solutions JV | Open Energy Information

    Open Energy Info (EERE)

    PNE Renewable Solutions JV Jump to: navigation, search Name: PNE & Renewable Solutions JV Place: Delaware Sector: Wind energy Product: Delaware-based limited liability company and...

  4. EQuilibrium Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    EQuilibrium Solutions Inc Jump to: navigation, search Name: eQuilibrium Solutions Inc Place: Boston, Massachusetts Zip: 2215 Sector: Carbon, Efficiency Product: Boston-based...

  5. Solargen Solutions UK | Open Energy Information

    Open Energy Info (EERE)

    Solargen Solutions UK Jump to: navigation, search Name: Solargen Solutions UK Place: United Kingdom Zip: NP 44 3AS Sector: Renewable Energy, Solar Product: String representation...

  6. Washington TRU Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Washington TRU Solutions Inc Jump to: navigation, search Name: Washington TRU Solutions, Inc. Place: Carlsbad, New Mexico Zip: 88220 Product: New Mexico-based managing and...

  7. Enisolar Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    Solutions Jump to: navigation, search Name: Enisolar Energy Solutions Place: Istanbul, Turkey Sector: Wind energy Product: Turkey-based wind, PV, and hybrid system integrator; also...

  8. Solar amp Electric Solutions | Open Energy Information

    Open Energy Info (EERE)

    Electric Solutions Jump to: navigation, search Name: Solar & Electric Solutions Place: Santa Cruz, California Zip: 95062 Sector: Solar Product: Small solar installation firm in...

  9. Global Warming Solutions Inc previously Southern Investments...

    Open Energy Info (EERE)

    Solutions Inc previously Southern Investments Inc Jump to: navigation, search Name: Global Warming Solutions Inc (previously Southern Investments Inc) Place: Houston, Texas...

  10. Quantum Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    Solutions Jump to: navigation, search Name: Quantum Energy Solutions Place: Rancho Cordova, California Zip: 95742 Product: California-based energy management company that was...

  11. Econic Renewable Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    Econic Renewable Energy Solutions Jump to: navigation, search Name: Econic Renewable Energy Solutions Place: Norfolk, United Kingdom Zip: NR 105PQ Sector: Renewable Energy Product:...

  12. Renewable Energy Solutions, LLC | Open Energy Information

    Open Energy Info (EERE)

    Solutions, LLC Jump to: navigation, search Name: Renewable Energy Solutions, LLC Place: Fairfield, California Zip: 94534 Region: Bay Area Sector: Services Year Founded: 2008...

  13. International Environmental Solutions IES | Open Energy Information

    Open Energy Info (EERE)

    Environmental Solutions IES Jump to: navigation, search Name: International Environmental Solutions (IES) Place: Romoland, California Zip: 92585 Product: It is an environmentally...

  14. M S Solutions | Open Energy Information

    Open Energy Info (EERE)

    Solutions Jump to: navigation, search Name: MS Solutions Place: Burdwan, West Bengal, India Sector: Biomass Product: Burdwan-based biomass cogenration project developer....

  15. Smarter Grid Solutions | Open Energy Information

    Open Energy Info (EERE)

    Smarter Grid Solutions Jump to: navigation, search Name: Smarter Grid Solutions Place: United Kingdom Product: String representation "The SGS technol ... the technology." is too...

  16. Eco Power Solutions | Open Energy Information

    Open Energy Info (EERE)

    Power Solutions Jump to: navigation, search Name: Eco Power Solutions Place: Quincy, Massachusetts Zip: 2169 Product: Massachusetts-based, energy recovery and emission control...

  17. Eco Sustainable Solutions Ltd | Open Energy Information

    Open Energy Info (EERE)

    Sustainable Solutions Ltd Jump to: navigation, search Name: Eco Sustainable Solutions Ltd Place: Dorset, United Kingdom Zip: BH23 6BG Sector: Biomass Product: Focused on organics...

  18. Presentation: Better Buildings Residential Program Solution Center...

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

    Presentation: Better Buildings Residential Program Solution Center, from the U.S. Department of Energy's Better Buildings Neighborhood Program, April 2014. Solution Center Overview...

  19. Solution Capital Partners | Open Energy Information

    Open Energy Info (EERE)

    Solution Capital Partners Jump to: navigation, search Name: Solution Capital Partners Place: New York Zip: NY 10036 Product: A New York-based investment firm active in the...

  20. Nextreme Thermal Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Nextreme Thermal Solutions Inc Jump to: navigation, search Name: Nextreme Thermal Solutions Inc Place: North Carolina Zip: 27709-3981 Product: String representation "Manufactures...

  1. Atlantic Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    Atlantic Energy Solutions Place: Foxboro, Massachusetts Sector: Efficiency, Renewable Energy Product: Atlantic Energy Solutions provides energy auditing for its customers and...

  2. Webinar Presentation: Energy Storage Solutions for Microgrids...

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

    Presentation: Energy Storage Solutions for Microgrids (November 2012) Webinar Presentation: Energy Storage Solutions for Microgrids (November 2012) On November 7, 2012, Clean ...

  3. Freedom Energy Solutions LLC | Open Energy Information

    Open Energy Info (EERE)

    Energy Solutions LLC Jump to: navigation, search Name: Freedom Energy Solutions LLC Place: Westminster, Maryland Zip: 21157 Sector: Geothermal energy, Solar Product: Retailer and...

  4. Consolidated Edison Solutions, Inc. ESCO Qualification Sheet...

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

    Consolidated Edison Solutions, Inc. ESCO Qualification Sheet Consolidated Edison Solutions, Inc. ESCO Qualification Sheet Document outlines the energy service company (ESCO)...

  5. Advanced Hydro Solutions | Open Energy Information

    Open Energy Info (EERE)

    Hydro Solutions Jump to: navigation, search Name: Advanced Hydro Solutions Place: Fairlawn, Ohio Zip: 44333 Sector: Hydro Product: Ohio-based company seeking to develop...

  6. Solution based temperature of Perovskite-type oxide films and powders

    SciTech Connect (OSTI)

    McHale, J.M. Jr.

    1995-04-01

    Conventional solid state reactions are diffusion limited processes that require high temperatures and long reaction times to reach completion. In this work, several solution based methods were utilized to circumvent this diffusion limited reaction and achieve product formation at lower temperatures. The solution methods studied all have the common goal of trapping the homogeneity inherent in a solution and transferring this homogeneity to the solid state, thereby creating a solid atomic mixture of reactants. These atomic mixtures can yield solid state products through {open_quotes}diffusionless{close_quotes} mechanisms. The effectiveness of atomic mixtures in solid state synthesis was tested on three classes of materials, varying in complexity. A procedure was invented for obtaining the highly water soluble salt, titanyl nitrate, TiO(NO{sub 3}){sub 2}, in crystalline form, which allowed the production of titanate materials by freeze drying. The freeze drying procedures yielded phase pure, nanocrystalline BaTiO{sub 3} and the complete SYNROC-B phase assemblage after ten minute heat treatments at 600{degrees}C and 1100{degrees}C, respectively. Two novel methods were developed for the solution based synthesis of Ba{sub 2}YCu{sub 3}O{sub 7-x} and Bi{sub 2}Sr{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10}. Thin and thick films of Ba{sub 2}YCu{sub 3}O{sub 7-x} and Bi{sub 2}Sr{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10} were synthesized by an atmospheric pressure, chemical vapor deposition technique. Liquid ammonia solutions of metal nitrates were atomized with a stream of N{sub 2}O and ignited with a hydrogen/oxygen torch. The resulting flame was used to coat a substrate with superconducting material. Bulk powders of Ba{sub 2}YCu{sub 3}O{sub 7-x} and Bi{sub 2}Sr{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10} were synthesized through a novel acetate glass method. The materials prepared were characterized by XRD, TEM, SEM, TGA, DTA, magnetic susceptibility and electrical resistivity measurements.

  7. Solution based synthesis of perovskite-type oxide films and powders

    SciTech Connect (OSTI)

    McHale, J.M. Jr.

    1995-01-01

    Conventional solid state reactions are diffusion limited processes that require high temperatures and long reaction times to reach completion. In this work, several solution based methods were utilized to circumvent this diffusion limited reaction and achieve product formation at lower temperatures. The solution methods studied all have the common goal of trapping the homogeneity inherent in a solution and transferring this homogeneity to the solid state, thereby creating a solid atomic mixture of reactants. These atomic mixtures can yield solid state products through diffusionless mechanisms. The effectiveness of atomic mixtures in solid state synthesis was tested on three classes of materials, varying in complexity. A procedure was invented for obtaining the highly water soluble salt, titanyl nitrate, TiO(NO{sub 3}){sub 2}, in crystalline form, which allowed the production of titanate materials by freeze drying. The freeze drying procedures yielded phase pure, nanocrystalline BaTiO{sub 3} and the complete SYNROC-B phase assemblage after ten minute heat treatments at 600 C and 1,100 C, respectively. Two novel methods were developed for the solution based synthesis of Ba{sub 2}YCu{sub 3}O{sub 7{minus}x} and Bi{sub 2}Sr{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10}. Thin and thick films of Ba{sub 2}YCu{sub 3}O{sub 7{minus}x} and Bi{sub 2}Sr{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10} were synthesized by an atmospheric pressure, chemical vapor deposition technique. Liquid ammonia solutions of metal nitrates were atomized with a stream of N{sub 2}O and ignited with a hydrogen/oxygen torch. The resulting flame was used to coat a substrate with superconducting material. Bulk powders of Ba{sub 2}YCu{sub 3}O{sub 7{minus}x} and Bi{sub 2}Sr{sub 2}Ca{sub 2}Cu{sub 3}O{sub 10} were synthesized through a novel acetate glass method. The materials prepared were characterized by XRD, TEM, SEM, TGA, DTA, magnetic susceptibility and electrical resistivity measurements.

  8. 2016 Midwest Energy Solutions Conference

    Broader source: Energy.gov [DOE]

    The Midwest Energy Efficiency Alliance invites all energy stakeholders to gather at the annual Midwest Energy Solutions Conference to raise awareness and reinforce the importance of energy efficiency in the Midwest. This annual conference is about celebrating accomplishments and inspirations in energy efficiency, as well as laying out the efficiency program and policy landscape for the coming year.

  9. 2016 Midwest Energy Solutions Conference

    Broader source: Energy.gov [DOE]

    Once a year, MEEA invites all energy stakeholders to gather at our annual Midwest Energy Solutions Conference to raise awareness and reinforce the importance of energy efficiency in the Midwest. MES is about celebrating accomplishments in energy efficiency, as well as laying out the efficiency program and policy landscape for the coming year.

  10. GADOLINIUM OXALATE SOLUBILITY MEASUREMENTS IN NITRIC ACID SOLUTIONS

    SciTech Connect (OSTI)

    Pierce, R. A.

    2012-03-12

    HB-Line will begin processing Pu solutions during FY2012 that will involve the recovery of Pu using oxalate precipitation and filtration. After the precipitation and filtration processes, the filtrate solution will be transferred from HB-Line to H-Canyon. The presence of excess oxalate and unfiltered Pu oxalate solids in these solutions create a criticality safety issue if they are sent to H-Canyon without controls in H-Canyon. One approach involves H-Canyon receiving the filtrate solution into a tank that is poisoned with soluble gadolinium (Gd). Decomposition of the oxalate will occur within a subsequent H-Canyon vessel. The receipt of excess oxalate into the H-Canyon receipt tanks has the potential to precipitate a portion of the Gd poison in the receipt tanks. Because the amount of Gd in solution determines the maximum amount of Pu solids that H-Canyon can receive, H-Canyon Engineering requested that SRNL determine the solubility of Gd in aqueous solutions of 4-10 M nitric acid (HNO{sub 3}), 4-12 g/L Gd, and 0.15-0.25 M oxalic acid (H{sub 2}C{sub 2}O{sub 4}) at 25 C. The target soluble Gd concentration is 6 g/L. The data indicate that the target can be achieved above 6 M HNO{sub 3} and below 0.25 M H{sub 2}C{sub 2}O{sub 4}. At 25 C, for 6 M HNO{sub 3}, 11 g/L and 7 g/L Gd are soluble in 0.15 M and 0.25 M H{sub 2}C{sub 2}O{sub 4}, respectively. In 4 M HNO{sub 3}, the Gd solubility drops significantly to 2.5 g/L and 0.8 g/L in 0.15 M and 0.25 M H{sub 2}C{sub 2}O{sub 4}, respectively. The solubility of Gd at 8-10 M HNO{sub 3} exceeds the solubility at 6 M HNO{sub 3}. The data for 4 M HNO{sub 3} showed good agreement with data in the literature. To achieve a target of 6 g/L soluble Gd in solution in the presence of 0.15-0.25 M oxalate, the HNO{sub 3} concentration must be maintained at or above 6 M HNO{sub 3}. The solubility of Gd in 4 M HNO{sub 3} with 0.15 M oxalate at 10 C is about 1.5 g/L. For 6 M HNO{sub 3} with 0.15 M oxalate, the solubility of Gd at 10 C is about 10 g/L. Gadolinium nitrate is very soluble in HNO{sub 3}. The solubility of Gd is linear as a function of HNO{sub 3} from 343 g/L Gd in 2.88 M HNO{sub 3} to 149 g/L in 8.16 M HNO{sub 3}. Below 2.88 M HNO{sub 3}, the solubility of Gd approaches a limit of about 360 g/L. However, there are no data available below 1.40 M HNO{sub 3}, which has a Gd solubility of 353 g/L.

  11. Analysis of the Fisher solution

    SciTech Connect (OSTI)

    Abdolrahimi, Shohreh; Shoom, Andrey A.

    2010-01-15

    We study the d-dimensional Fisher solution which represents a static, spherically symmetric, asymptotically flat spacetime with a massless scalar field. The solution has two parameters, the mass M and the 'scalar charge' {Sigma}. The Fisher solution has a naked curvature singularity which divides the spacetime manifold into two disconnected parts. The part which is asymptotically flat we call the Fisher spacetime, and another part we call the Fisher universe. The d-dimensional Schwarzschild-Tangherlini solution and the Fisher solution belong to the same theory and are dual to each other. The duality transformation acting in the parameter space (M,{Sigma}) maps the exterior region of the Schwarzschild-Tangherlini black hole into the Fisher spacetime which has a naked timelike singularity, and interior region of the black hole into the Fisher universe, which is an anisotropic expanding-contracting universe and which has two spacelike singularities representing its 'big bang' and 'big crunch'. The big bang singularity and the singularity of the Fisher spacetime are radially weak in the sense that a 1-dimensional object moving along a timelike radial geodesic can arrive to the singularities intact. At the vicinity of the singularity the Fisher spacetime of nonzero mass has a region where its Misner-Sharp energy is negative. The Fisher universe has a marginally trapped surface corresponding to the state of its maximal expansion in the angular directions. These results and derived relations between geometric quantities of the Fisher spacetime, the Fisher universe, and the Schwarzschild-Tangherlini black hole may suggest that the massless scalar field transforms the black hole event horizon into the naked radially weak disjoint singularities of the Fisher spacetime and the Fisher universe which are 'dual to the horizon'.

  12. REMOVAL OF CHLORIDE FROM AQUEOUS SOLUTIONS

    DOE Patents [OSTI]

    Schulz, W.W.

    1959-08-01

    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.

  13. Energy solutions?Director Eric Isaacs

    ScienceCinema (OSTI)

    Eric ISaacs

    2013-06-05

    Argonne's Director Eric Isaacs talks about the laboratory's efforts for creating new, clean energy solutions.

  14. Energy solutionsDirector Eric Isaacs

    SciTech Connect (OSTI)

    Eric ISaacs

    2012-08-08

    Argonne's Director Eric Isaacs talks about the laboratory's efforts for creating new, clean energy solutions.

  15. Isotopic identification of soil and permafrost nitrate sources in an Arctic tundra ecosystem

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Heikoop, Jeffrey M.; Throckmorton, Heather M.; Newman, Brent D.; Perkins, George B.; Iversen, Colleen M.; Chowdhury, Taniya Roy; Romanovsky, Vladimir E.; Graham, David E.; Norby, Richard J.; Wilson, Cathy J.; et al

    2015-06-08

    The nitrate (NO₃⁻) dual isotope approach was applied to snowmelt, tundra active layer pore waters, and underlying permafrost in Barrow, Alaska, USA, to distinguish between NO₃⁻ derived from at NO₃⁻ signal with δ¹⁵N averaging –4.8 ± 1.0‰ (standard error of the mean) and δ¹⁸O averaging 70.2 ±1.7‰. In active layer pore waters, NO₃⁻ primarily occurred at concentrations suitable for isotopic analysis in the relatively dry and oxic centers of high-centered polygons. The average δ¹⁵N and δ¹⁸O of NO₃⁻ from high-centered polygons were 0.5 ± 1.1‰ and –4.1 ± 0.6‰, respectively. When compared to the δ¹⁵N of reduced nitrogen (N) sources,more » and the δ¹⁸O of soil pore waters, it was evident that NO₃⁻ in high-centered polygons was primarily from microbial nitrification. Permafrost NO₃⁻ had δ¹⁵N ranging from approximately –6‰ to 10‰, similar to atmospheric and microbial NO₃⁻, and highly variable δ¹⁸O ranging from approximately –2‰ to 38‰. Permafrost ice wedges contained a significant atmospheric component of NO₃⁻, while permafrost textural ice contained a greater proportion of microbially derived NO₃⁻. Large-scale permafrost thaw in this environment would release NO₃⁻ with a δ¹⁸O signature intermediate to that of atmospheric and microbial NO₃. Consequently, while atmospheric and microbial sources can be readily distinguished by the NO₃⁻ dual isotope technique in tundra environments, attribution of NO₃⁻ from thawing permafrost will not be straightforward. The NO₃⁻ isotopic signature, however, appears useful in identifying NO₃⁻ sources in extant permafrost ice.« less

  16. Fluidized Bed Steam Reforming (FBSR) Mineralization for High Organic and Nitrate Waste Streams for the Global Nuclear Energy Partnership (GNEP)

    SciTech Connect (OSTI)

    Jantzen, C.M.; Williams, M.R. [Savannah River National Laboratory, Aiken, SC (United States)

    2008-07-01

    Waste streams that may be generated by the Global Nuclear Energy Partnership (GNEP) Advanced Energy Initiative may contain significant quantities of organics (0-53 wt%) and/or nitrates (0-56 wt%). Decomposition of high nitrate streams requires reducing conditions, e.g. organic additives such as sugar or coal, to reduce the NOx in the off-gas to N{sub 2} to meet the Clean Air Act (CAA) standards during processing. Thus, organics will be present during waste form stabilization regardless of which GNEP processes are chosen, e.g. organics in the feed or organics for nitrate destruction. High organic containing wastes cannot be stabilized with the existing HLW Best Developed Available Technology (BDAT) which is HLW vitrification (HLVIT) unless the organics are removed by preprocessing. Alternative waste stabilization processes such as Fluidized Bed Steam Reforming (FBSR) operate at moderate temperatures (650-750 deg. C) compared to vitrification (1150-1300 deg. C). FBSR converts organics to CAA compliant gases, creates no secondary liquid waste streams, and creates a stable mineral waste form that is as durable as glass. For application to the high Cs-137 and Sr-90 containing GNEP waste streams a single phase mineralized Cs-mica phase was made by co-reacting illite clay and GNEP simulated waste. The Cs-mica accommodates up to 30% wt% Cs{sub 2}O and all the GNEP waste species, Ba, Sr, Rb including the Cs-137 transmutation to Ba-137. For reference, the cesium mineral pollucite (CsAlSi{sub 2}O{sub 6}), currently being studied for GNEP applications, can only be fabricated at {>=}1000 deg. C. Pollucite mineralization creates secondary aqueous waste streams and NOx. Pollucite is not tolerant of high concentrations of Ba, Sr or Rb and forces the divalent species into different mineral host phases. The pollucite can accommodate up to 33% wt% Cs{sub 2}O. (authors)

  17. FLUIDIZED BED STEAM REFORMING MINERALIZATION FOR HIGH ORGANIC AND NITRATE WASTE STREAMS FOR THE GLOBAL NUCLEAR ENERGY PARTNERSHIP

    SciTech Connect (OSTI)

    Jantzen, C; Michael Williams, M

    2008-01-11

    Waste streams that may be generated by the Global Nuclear Energy Partnership (GNEP) Advanced Energy Initiative may contain significant quantities of organics (0-53 wt%) and/or nitrates (0-56 wt%). Decomposition of high nitrate streams requires reducing conditions, e.g. organic additives such as sugar or coal, to reduce the NO{sub x} in the off-gas to N{sub 2} to meet the Clean Air Act (CAA) standards during processing. Thus, organics will be present during waste form stabilization regardless of which GNEP processes are chosen, e.g. organics in the feed or organics for nitrate destruction. High organic containing wastes cannot be stabilized with the existing HLW Best Developed Available Technology (BDAT) which is HLW vitrification (HLVIT) unless the organics are removed by preprocessing. Alternative waste stabilization processes such as Fluidized Bed Steam Reforming (FBSR) operate at moderate temperatures (650-750 C) compared to vitrification (1150-1300 C). FBSR converts organics to CAA compliant gases, creates no secondary liquid waste streams, and creates a stable mineral waste form that is as durable as glass. For application to the high Cs-137 and Sr-90 containing GNEP waste streams a single phase mineralized Cs-mica phase was made by co-reacting illite clay and GNEP simulated waste. The Cs-mica accommodates up to 30% wt% Cs{sub 2}O and all the GNEP waste species, Ba, Sr, Rb including the Cs-137 transmutation to Ba-137. For reference, the cesium mineral pollucite (CsAlSi{sub 2}O{sub 6}), currently being studied for GNEP applications, can only be fabricated at {ge} 1000 C. Pollucite mineralization creates secondary aqueous waste streams and NO{sub x}. Pollucite is not tolerant of high concentrations of Ba, Sr or Rb and forces the divalent species into different mineral host phases. The pollucite can accommodate up to 33% wt% Cs{sub 2}O.

  18. Electrochromic salts, solutions, and devices

    DOE Patents [OSTI]

    Burrell, Anthony K. (Los Alamos, NM); Warner, Benjamin P. (Los Alamos, NM); McClesky,7,064,212 T. Mark (Los Alamos, NM)

    2006-06-20

    Electrochromic salts. Electrochromic salts of dicationic viologens such as methyl viologen and benzyl viologen associated with anions selected from bis(trifluoromethylsulfonyl)imide, bis(perfluoroethylsulfonyl)imide, and tris(trifluoromethylsulfonyl)methide are produced by metathesis with the corresponding viologen dihalide. They are highly soluble in molten quarternary ammonium salts and together with a suitable reductant provide electrolyte solutions that are used in electrochromic windows.

  19. Clean Energy Solutions Center (Presentation)

    SciTech Connect (OSTI)

    Reategui, S.

    2012-07-01

    The Clean Energy Ministerial launched the Clean Energy Solutions Center in April, 2011 for major economy countries, led by Australia and U.S. with other CEM partners. Partnership with UN-Energy is extending scope to support all developing countries: 1. Enhance resources on policies relating to energy access, small to medium enterprises (SMEs), and financing programs; 2. Offer expert policy assistance to all countries; 3. Expand peer to peer learning, training, and deployment and policy data for developing countries.

  20. Electrochromic Salts, Solutions, and Devices

    DOE Patents [OSTI]

    Burrell, Anthony K. (Los Alamos, NM); Warner, Benjamin P. (Los Alamos, NM); McClesky, T. Mark (Los Alamos, NM)

    2008-10-14

    Electrochromic salts. Electrochromic salts of dicationic viologens such as methyl viologen and benzyl viologen associated with anions selected from bis(trifluoromethylsulfonyl)imide, bis(perfluoroethylsulfonyl)imide, and tris(trifluoromethylsulfonyl)methide are produced by metathesis with the corresponding viologen dihalide. They are highly soluble in molten quarternary ammonium salts and together with a suitable reductant provide electrolyte solutions that are used in electrochromic windows.

  1. Electrochromic Salts, Solutions, and Devices

    DOE Patents [OSTI]

    Burrell, Anthony K. (Los Alamos, NM); Warner, Benjamin P. (Los Alamos, NM); McClesky, T. Mark (Los Alamos, NM)

    2008-11-11

    Electrochromic salts. Electrochromic salts of dicationic viologens such as methyl viologen and benzyl viologen associated with anions selected from bis(trifluoromethylsulfonyl)imide, bis(perfluoroethylsulfonyl)imide, and tris(trifluoromethylsulfonyl)methide are produced by metathesis with the corresponding viologen dihalide. They are highly soluble in molten quarternary ammonium salts and together with a suitable reductant provide electrolyte solutions that are used in electrochromic windows.

  2. Process for the extraction of technetium from uranium

    DOE Patents [OSTI]

    Gong, Cynthia-May S.; Poineau, Frederic; Czerwinski, Kenneth R.

    2010-12-21

    A spent fuel reprocessing method contacts an aqueous solution containing Technetium(V) and uranyl with an acidic solution comprising hydroxylamine hydrochloride or acetohydroxamic acid to reduce Tc(V) to Tc(II, and then extracts the uranyl with an organic phase, leaving technetium(II) in aqueous solution.

  3. Functionalized polymers for binding to solutes in aqueous solutions

    DOE Patents [OSTI]

    Smith, Barbara F.; Robison, Thomas W.

    2006-11-21

    A functionalized polymer for binding a dissolved molecule in an aqueous solution is presented. The polymer has a backbone polymer to which one or more functional groups are covalently linked. The backbone polymer can be such polymers as polyethylenimine, polyvinylamine, polyallylamine, and polypropylamine. These polymers are generally water-soluble, but can be insoluble when cross-linked. The functional group can be for example diol derivatives, polyol derivatives, thiol and dithiol derivatives, guest-host groups, affinity groups, beta-diphosphonic acids, and beta-diamides

  4. Commercial Lighting Solutions Webtool Peer Review Report, Office Solutions

    SciTech Connect (OSTI)

    Beeson, Tracy A.; Jones, Carol C.

    2010-02-01

    The Commercial Lighting Solutions (CLS) project directly supports the U.S. Department of Energys Commercial Building Energy Alliance efforts to design high performance buildings. CLS creates energy efficient best practice lighting designs for widespread use, and they are made available to users via an interactive webtool that both educates and guides the end user through the application of the Lighting Solutions. This report summarizes the peer review of the CLS webtool for offices. The methodology for the peer review process included data collection (stakeholder input), analysis of the comments, and organization of the input into categories for prioritization of the comments against a set of criteria. Based on this process, recommendations were developed for the release of version 2.0 of the webtool at the Lightfair conference in Las Vegas in May 2010. The report provides a list of the top ten most significant and relevant improvements that will be made within the webtool for version 2.0 as well as appendices containing the comments and short-term priorities in additional detail. Peer review comments that are considered high priority by the reviewers and the CLS team but cannot be completed for Version 2.0 are listed as long-term recommendations.

  5. Ferrocyanide Safety Project Dynamic X-Ray Diffraction studies of sodium nickel ferrocyanide reactions with equimolar nitrate/nitrite salts

    SciTech Connect (OSTI)

    Dodds, J.N. |

    1994-07-01

    Dynamic X-ray Diffraction (DXRD) has been to used to identify and quantify the solid state reactions that take place between sodium nickel ferrocyanide, Na{sub 2}NiFe(CN){sub 6}, and equimolar concentrations of sodium nitrate/nitrite, reactions of interest to the continued environmental safety of several large underground waste storage tanks at the Hanford site in eastern Washington. The results are supportive of previous work, which indicated that endothermic dehydration and melting of the nitrates take place before the occurrence of exothermic reactions that being about 300{degrees}C. The DXRD results show that a major reaction set at these temperatures is the occurrence of a series reaction that produces sodium cyanate, NaCNO, as an intermediate in a mildly exothermic first step. In the presence of gaseous oxygen, NaCNO subsequently reacts exothermally and at a faster rate to form metal oxides. Measurements of the rate of this reaction are used to estimate the heat release. Comparisons of this estimated heat release rate with heat transfer rates from a hypothetical ``hot spot`` show that, even in a worst-case scenario, the heat transfer rates are approximately eight times higher than the rate of energy release from the exothermic reactions.

  6. Preliminary safe-handling experiments on a mixture of cesium nickel ferrocyanide and equimolar sodium nitrate/nitrite

    SciTech Connect (OSTI)

    Scheele, R.D. ); Cady, H.H. )

    1992-01-01

    As part of the Hanford Site's evaluation of the potential hazards associated with the storage of ferrocyanide wastes generated when ferrocyanide was used to scavenge radiocesium from waste supernates in the 1950s, the Pacific Northwest Laboratory (PNL) subcontracted with Los Alamos National Laboratory (LANL) to perform a series of sensitivity tests. These test supplement PNL's thermal sensitivity testing results on the reactivity of cesium nickel ferrocyanide (Cs{sub 2}NiFe(CN){sub 6}) and nitrates and nitrites (Burger and Schelle 1991). LANL used a selected set of their standard tests to determine the sensitivity of a mixture of Cs{sub 2}NiFe(CN){sub 6} (FECN-1) and equimolar sodium nitrate and nitrite oxidant to nonthermal and thermal stimuli. The stoichiometric ratio of oxidant to Cs{sub 2}NiFe(CN){sub 6} in the tested mixture FECN-1 was 1.1:1. The appendix presents the results of the LANL testing of the sensitivity of FECN-1 to initiation by mechanical impact, spark, friction, and various thermal conditions. In addition to the sensitivity testing, LANL used an Accelerating Rate Calorimeter (ARC) to estimate the behavior of large batches of the mixture.

  7. Preliminary safe-handling experiments on a mixture of cesium nickel ferrocyanide and equimolar sodium nitrate/nitrite

    SciTech Connect (OSTI)

    Scheele, R.D.; Cady, H.H.

    1992-01-01

    As part of the Hanford Site`s evaluation of the potential hazards associated with the storage of ferrocyanide wastes generated when ferrocyanide was used to scavenge radiocesium from waste supernates in the 1950s, the Pacific Northwest Laboratory (PNL) subcontracted with Los Alamos National Laboratory (LANL) to perform a series of sensitivity tests. These test supplement PNL`s thermal sensitivity testing results on the reactivity of cesium nickel ferrocyanide (Cs{sub 2}NiFe(CN){sub 6}) and nitrates and nitrites (Burger and Schelle 1991). LANL used a selected set of their standard tests to determine the sensitivity of a mixture of Cs{sub 2}NiFe(CN){sub 6} (FECN-1) and equimolar sodium nitrate and nitrite oxidant to nonthermal and thermal stimuli. The stoichiometric ratio of oxidant to Cs{sub 2}NiFe(CN){sub 6} in the tested mixture FECN-1 was 1.1:1. The appendix presents the results of the LANL testing of the sensitivity of FECN-1 to initiation by mechanical impact, spark, friction, and various thermal conditions. In addition to the sensitivity testing, LANL used an Accelerating Rate Calorimeter (ARC) to estimate the behavior of large batches of the mixture.

  8. MOLECULAR APPROACHES FOR IN SITU IDENTIFCIATION OF NITRATE UTILIZATION BY MARINE BACTERIA AND PHYTOPLANKTON

    SciTech Connect (OSTI)

    Frischer, Marc E.; Verity, Peter G.; Gilligan, Mathew R.; Bronk, Deborah A.; Zehr, Jonathan P.; Booth, Melissa G.

    2013-09-12

    Traditionally, the importance of inorganic nitrogen (N) for the nutrition and growth of marine phytoplankton has been recognized, while inorganic N utilization by bacteria has received less attention. Likewise, organic N has been thought to be important for heterotrophic organisms but not for phytoplankton. However, accumulating evidence suggests that bacteria compete with phytoplankton for nitrate (NO3-) and other N species. The consequences of this competition may have a profound effect on the flux of N, and therefore carbon (C), in ocean margins. Because it has been difficult to differentiate between N uptake by heterotrophic bacterioplankton versus autotrophic phytoplankton, the processes that control N utilization, and the consequences of these competitive interactions, have traditionally been difficult to study. Significant bacterial utilization of DIN may have a profound effect on the flux of N and C in the water column because sinks for dissolved N that do not incorporate inorganic C represent mechanisms that reduce the atmospheric CO2 drawdown via the ?biological pump? and limit the flux of POC from the euphotic zone. This project was active over the period of 1998-2007 with support from the DOE Biotechnology Investigations ? Ocean Margins Program (BI-OMP). Over this period we developed a tool kit of molecular methods (PCR, RT-PCR, Q-PCR, QRT-PCR, and TRFLP) and combined isotope mass spectrometry and flow-cytometric approaches that allow selective isolation, characterization, and study of the diversity and genetic expression (mRNA) of the structural gene responsible for the assimilation of NO3- by heterotrophic bacteria (nasA). As a result of these studies we discovered that bacteria capable of assimilating NO3- are ubiquitous in marine waters, that the nasA gene is expressed in these environments, that heterotrophic bacteria can account for a significant fraction of total DIN uptake in different ocean margin systems, that the expression of nasA is differentially regulated in genetically distinct NO3- assimilating bacteria, and that the best predictors of nasA gene expression are either NO3- concentration or NO3- uptake rates. These studies provide convincing evidence of the importance of bacterial utilization of NO3-, insight into controlling processes, and provide a rich dataset that are being used to develop linked C and N modeling components necessary to evaluate the significance of bacterial DIN utilization to global C cycling. Furthermore, as a result of BI-OMP funding we made exciting strides towards institutionalizing a research and education based collaboration between the Skidaway Institute of Oceanography (SkIO) and Savannah State University (SSU), an historically black university within the University System of Georgia with undergraduate and now graduate programs in marine science. The BI-OMP program, in addition to supporting undergraduate (24) graduate (10) and postdoctoral (2) students, contributed to the development of a new graduate program in Marine Sciences at SSU that remains an important legacy of this project. The long-term goals of these collaborations are to increase the capacity for marine biotechnology research and to increase representation of minorities in marine, environmental and biotechnological sciences.

  9. Ultrafast studies of solution dynamics

    SciTech Connect (OSTI)

    Woodruff, W.H.; Dyer, R.B.; Callender, R.H.

    1997-10-01

    This is the final report of a one-year, Laboratory Directed Research and Development (LDRD) project at Los Alamos National Laboratory (LANL). Fast chemical dynamics generally must be initiated photochemically. This limits the applicability of modern laser methods for following the structural changes that occur during chemical and biological reactions to those systems that have an electronic chromophore that has a significant yield of photoproduct when excited. This project has developed a new and entirely general approach to ultrafast initiation of reactions in solution: laser-induced temperature jump (T-jump). The results open entire new fields of study of ultrafast molecular dynamics in solution. The authors have demonstrated the T-jump technique on time scales of 50 ps and longer, and have applied it to study of the fast events in protein folding. They find that a general lifetime of alpha-helix formation is ca 100 ns, and that tertiary folds (in apomyoglobin) form in ca 100 {mu}s.

  10. Eco Green Solutions | Open Energy Information

    Open Energy Info (EERE)

    Eco Green Solutions Place: Brazil Product: Brazil-based Ecodiesel creditor. References: Eco Green Solutions1 This article is a stub. You can help OpenEI by expanding it. Eco...

  11. Battery Wireless Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Solutions Inc Jump to: navigation, search Name: Battery & Wireless Solutions Inc Place: New Westminster, British Columbia, Canada Zip: V3M 5V9 Product: Distributor of battery and...

  12. Solar Project Solutions | Open Energy Information

    Open Energy Info (EERE)

    Solutions Place: California Sector: Solar Product: US-based JV to build solar-power plants in California. References: Solar Project Solutions1 This article is a stub. You can...

  13. EM Energy Solutions Ltd | Open Energy Information

    Open Energy Info (EERE)

    EM Energy Solutions Ltd Jump to: navigation, search Name: EM Energy Solutions Ltd Place: London, United Kingdom Zip: NW3 5QY Product: Consultant specialising in the development and...

  14. Westinghouse TRU Solutions Launches New Web Site

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

    TRU Solutions LLC Launches New Web Site CARLSBAD, N.M., February 2, 2001 - Westinghouse TRU Solutions LLC (WTS) today launched its new Web site. WTS is the new management and ...

  15. Washington River Protection Solutions - Hanford Site

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

    Contracting Washington River Protection Solutions Contracting ORP Contracts and Procurements RL Contracts and Procurements CH2M HILL Plateau Remediation Company Mission Support Alliance Washington Closure Hanford HPM Corporation (HPMC) Wastren Advantage, Inc. Bechtel National, Inc. Washington River Protection Solutions Washington River Protection Solutions Email Email Page | Print Print Page |Text Increase Font Size Decrease Font Size Washington River Protection Solutions, LLC logo The operation

  16. Presentation: Better Buildings Residential Program Solution Center

    Broader source: Energy.gov [DOE]

    Presentation: Better Buildings Residential Program Solution Center, from the U.S. Department of Energy, Better Buildings Neighborhood Program.

  17. Cleantech Solutions (Massachusetts) | Open Energy Information

    Open Energy Info (EERE)

    Massachusetts Zip: 02108 Region: Greater Boston Area Sector: Efficiency Product: Energy efficiency solutions and consumption monitoring systems for buildings Website:...

  18. Building America Solution Center | Department of Energy

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

    Building America Solution Center Building America Solution Center World-Class Research At Your Fingertips The Building America Solution Center provides residential building professionals with access to expert information on hundreds of high-performance design and construction topics, including air sealing and insulation, HVAC components, windows, indoor air quality, and much more. Explore the Building America Solution Center. The user-friendly interface delivers a variety of resources for each

  19. Clean Energy Solutions Center Services (Fact Sheet)

    SciTech Connect (OSTI)

    Not Available

    2014-04-01

    The Clean Energy Solutions Center (Solutions Center) helps governments, advisors and analysts create policies and programs that advance the deployment of clean energy technologies. The Solutions Center partners with international organizations to provide online training, expert assistance, and technical resources on clean energy policy.

  20. NOPR EnergySolutions | Department of Energy

    Office of Environmental Management (EM)

    EnergySolutions NOPR EnergySolutions PDF icon NOPR EnergySolutions More Documents & Publications Meeting Notes re NOI for Convention on Supplementary Compensation Enforcement Letter, NEL-2011-03 - October 24, 2011 EIS-0359: DOE Notice of Availability of the Draft Supplement Analysis

  1. Solution synthesis of germanium nanocrystals

    DOE Patents [OSTI]

    Gerung, Henry (Albuquerque, NM); Boyle, Timothy J. (Kensington, MD); Bunge, Scott D. (Cuyahoga Falls, OH)

    2009-09-22

    A method for providing a route for the synthesis of a Ge(0) nanometer-sized material from. A Ge(II) precursor is dissolved in a ligand heated to a temperature, generally between approximately 100.degree. C. and 400.degree. C., sufficient to thermally reduce the Ge(II) to Ge(0), where the ligand is a compound that can bond to the surface of the germanium nanomaterials to subsequently prevent agglomeration of the nanomaterials. The ligand encapsulates the surface of the Ge(0) material to prevent agglomeration. The resulting solution is cooled for handling, with the cooling characteristics useful in controlling the size and size distribution of the Ge(0) materials. The characteristics of the Ge(II) precursor determine whether the Ge(0) materials that result will be nanocrystals or nanowires.

  2. Regional Transmission Projects: Finding Solutions

    SciTech Connect (OSTI)

    The Keystone Center

    2005-06-15

    The Keystone Center convened and facilitated a year-long Dialogue on "Regional Transmission Projects: Finding Solutions" to develop recommendations that will help address the difficult and contentious issues related to expansions of regional electric transmission systems that are needed for reliable and economic transmission of power within and across regions. This effort brought together a cross-section of affected stakeholders and thought leaders to address the problem with the collective wisdom of their experience and interests. Transmission owners sat at the table with consumer advocates and environmental organizations. Representatives from regional transmission organizations exchanged ideas with state and federal regulators. Generation developers explored common interests with public power suppliers. Together, the Dialogue participants developed consensus solutions about how to begin unraveling some of the more intractable issues surrounding identification of need, allocation of costs, and reaching consensus on siting issues that can frustrate the development of regional transmission infrastructure. The recommendations fall into three broad categories: 1. Recommendations on appropriate institutional arrangements and processes for achieving regional consensus on the need for new or expanded transmission infrastructure 2. Recommendations on the process for siting of transmission lines 3. Recommendations on the tools needed to support regional planning, cost allocation, and siting efforts. List of Dialogue participants: List of Dialogue Participants: American Electric Power American Transmission Company American Wind Energy Association California ISO Calpine Corporation Cinergy Edison Electric Institute Environmental Defense Federal Energy Regulatory Commission Great River Energy International Transmission Company ISO-New England Iowa Public Utility Board Kanner & Associates Midwest ISO National Association of Regulatory Utility Commissioners National Association of State Utility Consumer Advocates National Grid Northeast Utilities PA Office of Consumer Advocates Pacific Gas & Electric Corporation Pennsylvania Public Utility Commission PJM Interconnection The Electricity Consumers Resource Council U.S. Department of Energy US Department of the Interior Van Ness Feldman Western Interstate Energy Board Wind on the Wires Wisconsin Public Service Commission Xcel Energy

  3. Nitrous oxide production from radiolysis of simulted high-level nuclear waste solutions

    SciTech Connect (OSTI)

    Walker, D.D.; Hobbs, D.T.; Tiffany, J.B.; Bibler, N.E.; Meisel, D.

    1992-07-01

    Nitrous oxide gas (N{sub 2}O) is produced by the radiolysis of aqueous nitrate or nitrite solutions in the presence of organic compounds. When ethylenediaminetetraacetic acid (EDTA) or N- (2-hydroxyethyl)-ethylenediaminetriacetic acid (HEDTA) is present, the G-value for hydrogen increases and N{sub 2}O become the major gaseous product (G=0.54). A survey of organic compounds indicates the amount of N{sub 2}O formed depends on the structure of the organic. With highly oxidized organics (carbonate, formate, acetate and oxalate), little or no N{sub 2}O is formed. Aromatic and aliphatic organics (sodium tetraphenylborate, benzene, phenol, n-paraffin, and tributylphosphate) produce small amounts of N{sub 2}O. Water soluble, easily oxidized organics (methanol, ethanol, isopropanol, n-butanol, acetone, and ethylene glycol) produce large amounts of N{sub 2}O relative to the previous two categories. Nitrous oxide production is not greatly affected by pH between neutral and pH=13, but increases significantly in acid solution. The G-value for N{sub 2}O production in 10 wt% potassium tetraphenylborate slurries has been measured under process conditions important at the Savannah River Site.

  4. Nitrous oxide production from radiolysis of simulted high-level nuclear waste solutions

    SciTech Connect (OSTI)

    Walker, D.D.; Hobbs, D.T.; Tiffany, J.B.; Bibler, N.E. ); Meisel, D. )

    1992-01-01

    Nitrous oxide gas (N{sub 2}O) is produced by the radiolysis of aqueous nitrate or nitrite solutions in the presence of organic compounds. When ethylenediaminetetraacetic acid (EDTA) or N- (2-hydroxyethyl)-ethylenediaminetriacetic acid (HEDTA) is present, the G-value for hydrogen increases and N{sub 2}O become the major gaseous product (G=0.54). A survey of organic compounds indicates the amount of N{sub 2}O formed depends on the structure of the organic. With highly oxidized organics (carbonate, formate, acetate and oxalate), little or no N{sub 2}O is formed. Aromatic and aliphatic organics (sodium tetraphenylborate, benzene, phenol, n-paraffin, and tributylphosphate) produce small amounts of N{sub 2}O. Water soluble, easily oxidized organics (methanol, ethanol, isopropanol, n-butanol, acetone, and ethylene glycol) produce large amounts of N{sub 2}O relative to the previous two categories. Nitrous oxide production is not greatly affected by pH between neutral and pH=13, but increases significantly in acid solution. The G-value for N{sub 2}O production in 10 wt% potassium tetraphenylborate slurries has been measured under process conditions important at the Savannah River Site.

  5. Temperature dependent DC electrical conductivity studies of ZnO nanoparticle thick films prepared by simple solution combustion method

    SciTech Connect (OSTI)

    Naveen, C. S. Jayanna, H. S. Lamani, Ashok R. Rajeeva, M. P.

    2014-04-24

    ZnO nanoparticles of different size were prepared by varying the molar ratio of glycine and zinc nitrate hexahydrate as fuel and oxidizer (F/O = 0.8, 1.11, 1.7) by simple solution combustion method. Powder samples were characterized by UV-Visible spectrophotometer, X-ray diffractometer, Scanning electron microscope (SEM). DC electrical conductivity measurements at room temperature and in the temperature range of 313-673K were carried out for the prepared thick films and it was found to increase with increase of temperature which confirms the semiconducting nature of the samples. Activation energies were calculated and it was found that, F/O molar ratio 1.7 has low E{sub AL} (Low temperature activation energy) and high E{sub AH} (High temperature activation energy) compared to other samples.

  6. Microsoft Word - DOE-ID-14-061 Cal-Berkeley EC B3-6.doc

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

    61 SECTION A. Project Title: Selective ligands for uranyl via combinatorial peptoid libraries: A synthetic, structural, thermodynamic and computational study - University of California Berkeley SECTION B. Project Description University of California Berkeley will conduct research aimed at developing a fundamental understanding of how donor ligands bind to the uranyl ion, UO2 2+, with the longer-term goal of using this information to tackle selective recognition of uranyl in aqueous solution.

  7. Coupled Fluid Energy Solute Transport

    Energy Science and Technology Software Center (OSTI)

    1992-02-13

    CFEST is a Coupled Fluid, Energy, and Solute Transport code for the study of a multilayered, nonisothermal ground-water system. It can model discontinuous as well as continuous layers, time-dependent and constant source/sinks, and transient as well as steady-state flow. The finite element method is used for analyzing isothermal and nonisothermal events in a confined aquifer system. Only single-phase Darcian flow is considered. In the Cartesian coordinate system, flow in a horizontal plane, in a verticalmore » plane, or in a fully three-dimensional region can be simulated. An option also exists for the axisymmetric analysis of a vertical cross section. The code employs bilinear quadrilateral elements in all two dimensional analyses and trilinear quadrilateral solid elements in three dimensional simulations. The CFEST finite element formulation can approximate discontinuities, major breaks in slope or thickness, and fault zones in individual hydrogeologic units. The code accounts for heterogeneity in aquifer permeability and porosity and accommodates anisotropy (collinear with the Cartesian coordinates). The variation in the hydraulic properties is described on a layer-by-layer basis for the different hydrogeologic units. Initial conditions can be prescribed hydraulic head or pressure, temperature, or concentration. CFEST can be used to support site, repository, and waste package subsystem assessments. Some specific applications are regional hydrologic characterization; simulation of coupled transport of fluid, heat, and salinity in the repository region; consequence assessment due to natural disruption or human intrusion scenarios in the repository region; flow paths and travel-time estimates for transport of radionuclides; and interpretation of well and tracer tests.« less

  8. Technical solutions to nonproliferation challenges

    SciTech Connect (OSTI)

    Satkowiak, Lawrence

    2014-05-09

    The threat of nuclear terrorism is real and poses a significant challenge to both U.S. and global security. For terrorists, the challenge is not so much the actual design of an improvised nuclear device (IND) but more the acquisition of the special nuclear material (SNM), either highly enriched uranium (HEU) or plutonium, to make the fission weapon. This paper provides two examples of technical solutions that were developed in support of the nonproliferation objective of reducing the opportunity for acquisition of HEU. The first example reviews technologies used to monitor centrifuge enrichment plants to determine if there is any diversion of uranium materials or misuse of facilities to produce undeclared product. The discussion begins with a brief overview of the basics of uranium processing and enrichment. The role of the International Atomic Energy Agency (IAEA), its safeguard objectives and how the technology evolved to meet those objectives will be described. The second example focuses on technologies developed and deployed to monitor the blend down of 500 metric tons of HEU from Russia's dismantled nuclear weapons to reactor fuel or low enriched uranium (LEU) under the U.S.-Russia HEU Purchase Agreement. This reactor fuel was then purchased by U.S. fuel fabricators and provided about half the fuel for the domestic power reactors. The Department of Energy established the HEU Transparency Program to provide confidence that weapons usable HEU was being blended down and thus removed from any potential theft scenario. Two measurement technologies, an enrichment meter and a flow monitor, were combined into an automated blend down monitoring system (BDMS) and were deployed to four sites in Russia to provide 24/7 monitoring of the blend down. Data was downloaded and analyzed periodically by inspectors to provide the assurances required.

  9. EA-306 MAG Energy Solutions, Inc. | Department of Energy

    Energy Savers [EERE]

    MAG Energy Solutions, Inc. EA-306 MAG Energy Solutions, Inc. Order authorizing MAG Energy Solutions, Inc. to export electric energy to Canada PDF icon EA-306 MAG Energy Solutions, Inc. More Documents & Publications EA-306-B MAG Energy Solutions, Inc. EA-306-A MAG Energy Solutions, Inc. Application to Export Electric Energy OE Docket No. EA-306-A MAG Energy Solutions

  10. Supergravity solutions without triholomorphic U(1) isometries

    SciTech Connect (OSTI)

    Ghezelbash, A. M.

    2008-12-15

    We investigate the construction of five-dimensional supergravity solutions that do not have any triholomorphic U(1) isometries. We construct a class of solutions that in various limits of parameters reduces to many of previously constructed five-dimensional supergravity solutions based on both hyper-Kaehler base spaces that can be put into a Gibbons-Hawking form and hyper-Kaehler base spaces that cannot be put into a Gibbons-Hawking form. We find a new solution which is over triaxial Bianchi type IX Einstein-hyper-Kaehler base space with no triholomorphic U(1) symmetry. One special case of this solution corresponds to a five-dimensional solution based on Eguchi-Hanson type II geometry.

  11. Energy Solutions Conference | Department of Energy

    Energy Savers [EERE]

    Energy Solutions Conference Energy Solutions Conference March 23, 2016 9:00AM EDT to March 24, 2016 4:00PM EDT Online The virtual Energy Solutions Conference will be held March 23-24, 2016. Bioenergy Technologies Office Director Jonathan Male will be giving a virtual presentation on the Office's activities supporting the federal bioeconomy as part of the renewable energy portion of the program.

  12. Integrated Engineering, Construction, and Management Solutions

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

    Integrated Engineering, Construction, and Management Solutions Washington Group International Contact: Susan Scott Public Affairs (505) 234-7204 http://www.wipp.ws Washington TRU Solutions LLC Washington TRU Solutions LLC Waste Isolation Pilot Plant Waste Isolation Pilot Plant P.O. Box 2078 P.O. Box 2078 Carlsbad, New Mexico 88221 Carlsbad, New Mexico 88221 For immediate release For immediate release Firm Awarded WIPP Records Demonstration Contract CARLSBAD, N.M., February 17, 2005 - Washington

  13. RECOVERY OF TETRAVALENT CATIONS FROM AQUEOUS SOLUTIONS

    DOE Patents [OSTI]

    Moore, R.L.

    1958-05-01

    The recovery of plutonium, zirconium, and tetravalent cerium values from aqueous solutions is described. It consists of adding an alkyl phosphate to a nnineral acid aqueous solution containing the metal to be recovered, whereby a precipitate forms with the tetravalent values, and separating the precipitate from the solution. All alkyl phosphates, if water-soluble, are suitable for the process; however, monobutyl phosphate has been found best.

  14. Energy Technology Solutions | Department of Energy

    Office of Environmental Management (EM)

    Technology Solutions Energy Technology Solutions Public-private partnerships transforming industry and list of commercialized technologies, knowledge-based results, and promising technologies PDF icon itp_successes.pdf More Documents & Publications Energy Technology Solutions: Public-Private Partnerships Transforming Industry, November 2010 ITP Energy Intensive Processes: Energy-Intensive Processes Portfolio: Addressing Key Energy Challenges Across U.S. Industry Energy-Intensive Processes

  15. Tangent Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    Jump to: navigation, search Name: Tangent Energy Solutions Place: Pennsylvania Zip: PA 19348 Product: Pennsylvania-based company developing and implementing sustainable energy...

  16. DG Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    92101 Product: Develops owns and operates industrial, commercial and institutional cogeneration plants from 2-50MW. References: DG Energy Solutions1 This article is a stub. You...

  17. Building America Technology Solutions Case Study: Combustion...

    Energy Savers [EERE]

    Combustion Safety Simplified Test Protocol Building America Technology Solutions Case Study: Combustion Safety Simplified Test Protocol Two U.S. Department of Energy Building ...

  18. Building America Technology Solutions Case Study: Ventilation...

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

    Case Study: Ventilation System Effectiveness and Tested Indoor Air Quality Impacts Building America Technology Solutions Case Study: Ventilation System Effectiveness and Tested ...

  19. EnergySolutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Salt Lake City, Utah Zip: 84101 Sector: Services Product: Utah-based international nuclear services company that provides services and solutions to the nuclear industry....

  20. Better Buildings Residential Program Solution Center Demonstration...

    Office of Environmental Management (EM)

    Program Solution Center Vehicle Technologies Office Merit Review 2014: A Combined Experimental and Modeling Approach for the Design of High Coulombic Efficiency Si Electrodes...

  1. Miniaturized Turbine Offers Desalination Solution | GE Global...

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

    from ice New solution draws from the GE Store, integrating GE's experience with steam turbine, oil & gas compressors, 3D printing and water processing NISKAYUNA, NY, November 10,...

  2. Energy Solutions S A | Open Energy Information

    Open Energy Info (EERE)

    Solutions S.A. Place: PERNIK, Bulgaria Zip: 2304 Sector: Solar Product: produces photovoltaic modules using mono- and poly-crystalline Si solar cells. Crystalline Si...

  3. Enterprise Solar Solutions | Open Energy Information

    Open Energy Info (EERE)

    Sector: Solar Product: New York-based company that specializes in commercial solar photovoltaic applications for businesses. References: Enterprise Solar Solutions1 This article...

  4. TVA- Energy Right Solutions for Business

    Broader source: Energy.gov [DOE]

    TVA offers the Energy Right Solutions Program to commercial and industrial facilities. In addition to prescriptive rebates for lighting, motors, HVAC, and kitchen equipment, administrators take a...

  5. TVA- Energy Right Solutions for Business

    Broader source: Energy.gov [DOE]

    The Tennessee Valley Authority (TVA) offers the Energy Right Solutions Program for commercial and industrial facilities.  Prescriptive rebates are available for lighting, motors, HVAC, and kitchen...

  6. Mobile Power Solutions | Open Energy Information

    Open Energy Info (EERE)

    laboratory focused on United NationsDepartment of Transportation compliance and battery performance testing. References: Mobile Power Solutions1 This article is a stub....

  7. Advanced Combustion Concepts - Enabling Systems and Solutions...

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

    (ACCESS) for High Efficiency Light Duty Vehicles Vehicle Technologies Office Merit Review 2014: Advanced Combustion Concepts - Enabling Systems and Solutions (ACCESS) for ...

  8. SMECO- Small Business/Non-Profit Solutions

    Broader source: Energy.gov [DOE]

    Southern Maryland Electric Cooperative (SMECO) offers Small Business Solutions program, which provides incentives up to 80% of the cost of retrofit projects for qualified small business and non...

  9. Better Buildings Residential Program Solution Center Demonstration...

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

    Transcript The Better Buildings Residential Program Solution Center is a robust online collection of nearly 1,000 examples, strategies, and resources from Better Buildings...

  10. Independent Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    navigation, search Name: Independent Energy Solutions Address: 1090 Joshua Way Place: Vista, California Zip: 92081 Region: Southern CA Area Sector: Solar Product: Renewable...

  11. Infinite Power Solutions | Open Energy Information

    Open Energy Info (EERE)

    Colorado Zip: 80127 Product: Littleton-based solid-state, rechargeable thin-film micro-energy storage device manufacturer. References: Infinite Power Solutions1 This article...

  12. Community Renewable Solutions LLC | Open Energy Information

    Open Energy Info (EERE)

    LLC Jump to: navigation, search Name: Community Renewable Solutions LLC Place: Santa Barbara, California Phone Number: 805 284 9028 Website: www.communityrenewables.biz...

  13. Innovative Energy Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Innovative Energy Solutions Inc Place: Las Vegas, Nevada Zip: 89101 Sector: Hydro, Hydrogen Product: Holds serveral patents related to waste heat recovery, heat generating...

  14. NCRC Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    search Name: NCRC Energy Solutions Place: Plano, Texas Zip: 75093 Sector: Hydro, Hydrogen Product: Developed and controls all rights to a proprietary software application...

  15. New Energy Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Energy Solutions Inc Place: Pittsfield, Massachusetts Zip: MA 01201 Sector: Hydro, Hydrogen Product: Small private new energy company active in the fuel cell, hydrogen and wave...

  16. ECO2 Asset Solutions | Open Energy Information

    Open Energy Info (EERE)

    Asset Solutions Place: Tampa, Florida Sector: Carbon, Services Product: Florida-based provider of advisory services to both buyers and sellers on the Carbon Markets. They serve a...

  17. Stellar Energy Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    California Zip: 95448 Sector: Renewable Energy, Solar Product: Turn-key renewable energy solutions provider specializing in solar electric roofing. References: Stellar...

  18. Basic energy properties of electrolytic solutions database. ...

    Office of Scientific and Technical Information (OSTI)

    Basic energy properties of electrolytic solutions database. Viscosity, thermal conductivity, density, enthalpy Citation Details In-Document Search Title: Basic energy properties...

  19. New Grid Energy Solutions | Open Energy Information

    Open Energy Info (EERE)

    Energy Solutions Address: 3704 Macomb St Place: Washington DC Zip: 20016 Sector: Biomass, Buildings, Efficiency, Geothermal energy, Services, Solar Product: Renewable Energy and...

  20. Solar India Solutions | Open Energy Information

    Open Energy Info (EERE)

    Visakhapatnam, Andhra Pradesh, India Zip: 530016 Sector: Efficiency Product: Andhra-based energy efficiency consultant. References: Solar India Solutions1 This article is a stub....

  1. Natural Solutions Pvt Ltd | Open Energy Information

    Open Energy Info (EERE)

    Jump to: navigation, search Name: Natural Solutions Pvt. Ltd. Place: Mumbai, Maharashtra, India Sector: Renewable Energy Product: Mumbai-based IT consultant. The firm plans to set...

  2. ITP Aluminum: Aluminum Industry Vision: Sustainable Solutions...

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

    Solutions for a Dynamic World PDF icon alumvision.pdf More Documents & Publications ITP Aluminum: Alumina Technology Roadmap U.S. Energy Requirements for Aluminum Production...

  3. El Paso Electric Company- Residential Solutions Program

    Broader source: Energy.gov [DOE]

    The El Paso Electric Residential Solutions Program offers El Paso Electric customers and participating contractors cash and non-cash incentives for implementing energy efficiency improvements in...

  4. Removal of radioisotopes from waste solutions

    DOE Patents [OSTI]

    Kirby, H.W.

    1973-10-01

    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)

  5. Energy Solutions International | Open Energy Information

    Open Energy Info (EERE)

    Jump to: navigation, search Name: Energy Solutions International Place: St. Paul, Minnesota Zip: 55107 Product: For the last decade, ESI has been creating fluorescent...

  6. Bringing Solutions to the Developing World

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

    low-cost, sustainable solutions to the problem accompanied by an innovative business model that is informed by culturally relevant data, lessons from failed technologies and...

  7. Presentation: Better Buildings Residential Program Solution Center

    Broader source: Energy.gov [DOE]

    Presentation: Better Buildings Residential Program Solution Center, from the U.S. Department of Energy's Better Buildings Neighborhood Program, April 2014.

  8. Cleantech Solutions (Colorado) | Open Energy Information

    Open Energy Info (EERE)

    Place: Boulder, Colorado Zip: 80301 Region: Rockies Area Sector: Efficiency Product: Energy efficiency solutions and consumption monitoring systems for buildings Website:...

  9. H I Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Zip: 30144-1299 Product: Building Management Systems solutions company, providing computer based automation systems for industrial, commercial, office, retail, educational and...

  10. Engineered Solutions: Order (2010-CE-2112)

    Broader source: Energy.gov [DOE]

    DOE issued an Order after entering into a Compromise Agreement with Engineered Solutions, Inc. to resolve a case involving the failure to certify dehumidifier basic model SD109.

  11. Engineered Solutions: Proposed Penalty (2010-CE-2112)

    Broader source: Energy.gov [DOE]

    DOE alleged in a Notice of Proposed Civil Penalty that Engineered Solutions, Inc. failed to certify a dehumidifier as compliant with the applicable energy conservation standards.

  12. Green Heat Solutions Limited | Open Energy Information

    Open Energy Info (EERE)

    to: navigation, search Name: Green Heat Solutions Limited Region: Scotland Sector: Marine and Hydrokinetic Website: http: This company is listed in the Marine and Hydrokinetic...

  13. Building America Technology Solutions for New and Existing Homes...

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

    Technology Solutions for New Manufactured Homes - Washington, Oregon, and Idaho Building America Technology Solutions for New and Existing Homes: Technology Solutions for New ...

  14. CO2 Global Solutions International | Open Energy Information

    Open Energy Info (EERE)

    Global Solutions International Jump to: navigation, search Name: CO2 Global Solutions International Place: Madrid, Spain Zip: 28001 Sector: Carbon Product: CO2 Global Solutions is...

  15. Clean Energy Solutions Centers Fact Sheet | Department of Energy

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

    A fact sheet describing the mission of the Clean Energy Solution Center. Clean Energy Solutions Centers Fact Sheet More Documents & Publications Clean-Energy-Solutions-Centers-Fact...

  16. Soleil Energy Solutions Greensboro North Carolina | Open Energy...

    Open Energy Info (EERE)

    Soleil Energy Solutions Greensboro North Carolina Jump to: navigation, search Logo: Soleil Energy Solutions Greensboro North Carolina Name: Soleil Energy Solutions Greensboro North...

  17. GE Lighting Solutions: Order (2013-SE-4901)

    Broader source: Energy.gov [DOE]

    DOE ordered General Electric Lighting Solutions, LLC to pay a $5,360 civil penalty after finding GE Lighting Solutions had manufactured and distributed in commerce in the U.S. 30 units of basic model DR4-RTFB-23B and 177 units (of which 85 units remain in inventory) of basic model DR4-RTFB-77A-002, noncompliant traffic signal modules.

  18. Zinc Bromide Waste Solution Treatment Options

    SciTech Connect (OSTI)

    Langston, C.A.

    2001-01-16

    The objective of this effort was to identify treatment options for 20,000 gallons of low-level radioactively contaminated zinc bromide solution currently stored in C-Area. These options will be relevant when the solutions are declared waste.

  19. Novel Nanostructured Interface Solution for Automotive Thermoelectric

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

    Modules Application | Department of Energy Nanostructured Interface Solution for Automotive Thermoelectric Modules Application Novel Nanostructured Interface Solution for Automotive Thermoelectric Modules Application Presents nanostructured thermal/electrical interface tapeŽ concept involving carbon nanotube and metal nanowire films to improve thermomechanical cycling behavior of automotive TEGs PDF icon asheghi.pdf More Documents & Publications Thermoelectrics Partnership: Automotive

  20. Conference Agenda: Residential Energy Efficiency Solutions 2012 |

    Office of Environmental Management (EM)

    Department of Energy Conference Agenda: Residential Energy Efficiency Solutions 2012 Conference Agenda: Residential Energy Efficiency Solutions 2012 Presents conference agenda including a general overview and detailed breakouts. PDF icon Conference Agenda More Documents & Publications Draft Agenda for U.S.-Africa Energy Ministerial Biomass 2009 Conference Agenda Biomass 2011 Conference Agenda

  1. PROCESSES OF RECLAIMING URANIUM FROM SOLUTIONS

    DOE Patents [OSTI]

    Zumwalt, L.R.

    1959-02-10

    A process is described for reclaiming residual enriched uranium from calutron wash solutions containing Fe, Cr, Cu, Ni, and Mn as impurities. The solution is adjusted to a pH of between 2 and 4 and is contacted with a metallic reducing agent, such as iron or zinc, in order to reduce the copper to metal and thereby remove it from the solution. At the same time the uranium present is reduced to the uranous state The solution is then contacted with a precipitate of zinc hydroxide or barium carbonate in order to precipitate and carry uranium, iron, and chromium away from the nickel and manganese ions in the solution. The uranium is then recovered fronm this precipitate.

  2. Reference electrode for strong oxidizing acid solutions

    DOE Patents [OSTI]

    Rigdon, Lester P. (Livermore, CA); Harrar, Jackson E. (Castro Valley, CA); Bullock, Sr., Jack C. (Pleasanton, CA); McGuire, Raymond R. (Brentwood, CA)

    1990-01-01

    A reference electrode for the measurement of the oxidation-reduction potentials of solutions is especially suitable for oxidizing solutions such as highly concentrated and fuming nitric acids, the solutions of nitrogen oxides, N.sub.2 O.sub.4 and N.sub.2 O.sub.5, in nitric acids. The reference electrode is fabricated of entirely inert materials, has a half cell of Pt/Ce(IV)/Ce(III)/70 wt. % HNO.sub.3, and includes a double-junction design with an intermediate solution of 70 wt. % HNO.sub.3. The liquid junctions are made from Corning No. 7930 glass for low resistance and negligible solution leakage.

  3. Extraction of uranium from spent fuels using liquefied gases

    SciTech Connect (OSTI)

    Sawada, Kayo; Hirabayashi, Daisuke; Enokida, Youichi

    2007-07-01

    For reprocessing of spent nuclear fuels, a novel method to extract actinides from spent fuel using highly compressed gases, nitrogen dioxide and carbon dioxide was proposed. As a fundamental study, the nitrate conversion with liquefied nitrogen dioxide and the nitrate extraction with supercritical carbon dioxide were demonstrated by using uranium dioxide powder, uranyl nitrate and tri-n-butylphosphate complex in the present study. (authors)

  4. Microbial Activity and Precipitation at Solution-Solution Mixing Zones in

    Office of Scientific and Technical Information (OSTI)

    Porous Media -- Subsurface Biogeochemical Research (Technical Report) | SciTech Connect Microbial Activity and Precipitation at Solution-Solution Mixing Zones in Porous Media -- Subsurface Biogeochemical Research Citation Details In-Document Search Title: Microbial Activity and Precipitation at Solution-Solution Mixing Zones in Porous Media -- Subsurface Biogeochemical Research The goal for this research was to understand how best to add compounds to receptive microbial communities in porous

  5. Energy Technology Solutions: Public-Private Partnerships Transforming...

    Energy Savers [EERE]

    Energy Technology Solutions: Public-Private Partnerships Transforming Industry, November 2010 Energy Technology Solutions: Public-Private Partnerships Transforming Industry,...

  6. Environmental Management and Planning Solutions, Inc | Open Energy...

    Open Energy Info (EERE)

    Environmental Management and Planning Solutions, Inc Jump to: navigation, search Name: Environmental Management and Planning Solutions, Inc Abbreviation: EMPSi Website:...

  7. WIPP Weatherization: Common Errors and Innovative Solutions Presentati...

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

    WIPP Weatherization: Common Errors and Innovative Solutions Presentation WIPP Weatherization: Common Errors and Innovative Solutions Presentation This presentation contains...

  8. EA-284-A Sempra Energy Solutions: Temporary Extension | Department of

    Energy Savers [EERE]

    Energy A Sempra Energy Solutions: Temporary Extension EA-284-A Sempra Energy Solutions: Temporary Extension Temporary extension of order authorizing Sempra Energy Solutions to export electric energy to mexico. PDF icon EA-284-A Sempra Energy Solutions More Documents & Publications EA-284-A Sempra Energy Solutions EA-406 Sempra Generation, LLC EA-284-C NOBLE AMERICAS ENERGY SOLUTIONS LLC

  9. EA-284-A Sempra Energy Solutions | Department of Energy

    Office of Environmental Management (EM)

    4-A Sempra Energy Solutions EA-284-A Sempra Energy Solutions Order authorizing Sempra Energy Solutions to export electric energy to Mexico. PDF icon EA-284-A Sempra Energy Solutions More Documents & Publications EA-284-A Sempra Energy Solutions: Temporary Extension EA-406 Sempra Generation, LLC EA-284-C NOBLE AMERICAS ENERGY SOLUTIONS LLC

  10. Nitrogen isotopes as indicators of NOx source contributions to atmospheric nitrate deposition across the Midwestern and Northeastern United States

    SciTech Connect (OSTI)

    E.M. Elliott; C. Kendall; S.D. Wanke; D.A. Burns; E.W. Boyer; K. Harlin; D.J. Bain; T.J. Butler

    2007-11-15

    Global inputs of NOx are dominated by fossil fuel combustion from both stationary and vehicular sources and far exceed natural NOx sources. However, elucidating NOx sources to any given location remains a difficult challenge, despite the need for this information to develop sound regulatory and mitigation strategies. We present results from a regional-scale study of nitrogen isotopes (15N) in wet nitrate deposition across 33 sites in the midwestern and northeastern U.S. We demonstrate that spatial variations in 15N are strongly correlated with NOx emissions from surrounding stationary sources and additionally that 15N is more strongly correlated with surrounding stationary source NOx emissions than pH, SO{sub 4}{sup 2-}, or NO{sub 3}{sup -} concentrations. Although emission inventories indicate that vehicle emissions are the dominant NOx source in the eastern U.S., our results suggest that wet NO{sub 3}{sup -} deposition at sites in this study is strongly associated with NOx emissions from power plants. This suggests that large areas of the landscape potentially receive atmospheric NOy deposition inputs in excess of what one would infer from existing monitoring data alone. Moreover, we determined that spatial patterns in 15N values are a robust indicator of stationary NOx contributions to wet NO{sub 3}{sup -} deposition and hence a valuable complement to existing tools for assessing relationships between NO{sub 3}{sup -} deposition, regional emission inventories, and for evaluating progress toward NOx reduction goals. 44 refs., 3 figs.

  11. Stabilization of polyaniline solutions through additives

    DOE Patents [OSTI]

    Wrobleski, Debra A. (Los Alamos, NM); Benicewicz, Brian C. (Los Alamos, NM)

    1996-01-01

    A stabilized non-conductive polyaniline solution comprising from about 1 to bout 10 percent by weight polyaniline or a polyaniline derivative, from about 90 to about 99 percent by weight N-methylpyrrolidone, and from about 0.5 percent by weight to about 15 percent by weight of a solution stabilizing additive selected from the group consisting of hindered amine light stabilizers, polymeric amines, and dialkylamines, percent by weight of additive based on the total weight of polyaniline or polyaniline derivative is provided together with a method for stabilizing a polyaniline solution.

  12. Stabilization of polyaniline solutions through additives

    DOE Patents [OSTI]

    Wrobleski, D.A.; Benicewicz, B.C.

    1996-12-10

    A stabilized non-conductive polyaniline solution comprising from about 1 to about 10 percent by weight polyaniline or a polyaniline derivative, from about 90 to about 99 percent by weight N-methylpyrrolidone, and from about 0.5 percent by weight to about 15 percent by weight of a solution stabilizing additive selected from the group consisting of hindered amine light stabilizers, polymeric amines, and dialkylamines, percent by weight of additive based on the total weight of polyaniline or polyaniline derivative is provided together with a method for stabilizing a polyaniline solution. 4 figs.

  13. Supersymmetric Kerr-anti-de Sitter solutions

    SciTech Connect (OSTI)

    Cvetic, Mirjam; Gao Peng; Simon, Joan

    2005-07-15

    We prove the existence of one quarter supersymmetric type IIB configurations that arise as nontrivial scaling solutions of the standard five-dimensional Kerr-anti-de Sitter black holes by the explicit construction of its Killing spinors. This neutral, spinning solution is asymptotic to the static anti-de Sitter space-time with cosmological constant -(1/l{sup 2}), it has two finite equal angular momenta J{sub 1}={+-}J{sub 2}, mass M=(1/l)(|J{sub 1}|+|J{sub 2}|) and a naked singularity. We also address the scaling limit associated with one-half supersymmetric solution with only one angular momentum.

  14. Membrane separation of ionic liquid solutions

    DOE Patents [OSTI]

    Campos, Daniel; Feiring, Andrew Edward; Majumdar, Sudipto; Nemser, Stuart

    2015-09-01

    A membrane separation process using a highly fluorinated polymer membrane that selectively permeates water of an aqueous ionic liquid solution to provide dry ionic liquid. Preferably the polymer is a polymer that includes polymerized perfluoro-2,2-dimethyl-1,3-dioxole (PDD). The process is also capable of removing small molecular compounds such as organic solvents that can be present in the solution. This membrane separation process is suitable for drying the aqueous ionic liquid byproduct from precipitating solutions of biomass dissolved in ionic liquid, and is thus instrumental to providing usable lignocellulosic products for energy consumption and other industrial uses in an environmentally benign manner.

  15. Separation of metal ions from aqueous solutions

    DOE Patents [OSTI]

    Almon, Amy C. (Augusta, GA)

    1994-01-01

    A process and apparatus for quantitatively and selectively separating metal ions from mixtures thereof in aqueous solution. The apparatus includes, in combination, a horizontal electrochemical flow cell containing flow bulk electrolyte solution and an aqueous, metal ion-containing solution, the cell containing a metal mesh working electrode, a counter electrode positioned downstream from the working electrode, an independent variable power supply/potentiostat positioned outside of the flow cell and connected to the electrodes, and optionally a detector such as a chromatographic detector, positioned outside the flow cell. This apparatus and its operation has significant application where trace amounts of metal ions are to be separated.

  16. Concentration of perrhenate and pertechnetate solutions

    DOE Patents [OSTI]

    Knapp, F.F.; Beets, A.L.; Mirzadeh, S.; Guhlke, S.

    1998-03-17

    A method is described for preparing a concentrated solution of a carrier-free radioisotope which includes the steps of: (a) providing a generator column loaded with a composition containing a parent radioisotope; (b) eluting the generator column with an eluent solution which includes a salt of a weak acid to elute a target daughter radioisotope from the generator column in a first eluate; (c) eluting a cation-exchange column with the first eluate to exchange cations of the salt for hydrogen ions and to elute the target daughter radioisotope and a weak acid in a second eluate; (d) eluting an anion-exchange column with the second eluate to trap and concentrate the target daughter radioisotope and to elute the weak acid solution therefrom; and (e) eluting the concentrated target daughter radioisotope from the anion-exchange column with a saline solution. 1 fig.

  17. TVA- Energy Right Solutions for Business

    Broader source: Energy.gov [DOE]

    TVA offers the Energy Right Solutions Program to commercial and industrial facilities.  In addition to prescriptive rebates for lighting, motors, HVAC, and kitchen equipment, administrators take a...

  18. WM Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Los Angeles, California Product: Owns and operates a landfill gas plant located at Bradley Landfill. References: WM Solutions Inc1 This article is a stub. You can help OpenEI...

  19. Glendale Water and Power- Solar Solutions Program

    Broader source: Energy.gov [DOE]

    The Solar Solutions program provides all customer groups with an incentive to install photovoltaic (PV) systems on their homes and buildings. Rebate levels will decrease over time on an annual...

  20. Lightweight Steel Solutions for Automotive Industry

    SciTech Connect (OSTI)

    Lee, Hong Woo; Kim, Gyosung; Park, Sung Ho

    2010-06-15

    Recently, improvement in fuel efficiency and safety has become the biggest issue in worldwide automotive industry. Although the regulation of environment and safety has been tightened up more and more, the majority of vehicle bodies are still manufactured from stamped steel components. This means that the optimized steel solutions enable to demonstrate its ability to reduce body weight with high crashworthiness performance instead of expensive light weight materials such as Al, Mg and composites. To provide the innovative steel solutions for automotive industry, POSCO has developed AHSS and its application technologies, which is directly connected to EVI activities. EVI is a technical cooperation program with customer covering all stages of new car project from design to mass production. Integrated light weight solutions through new forming technologies such as TWB, hydroforming and HPF are continuously developed and provided for EVI activities. This paper will discuss the detailed status of these technologies especially light weight steel solutions based on innovative technologies.

  1. Concentration of perrhenate and pertechnetate solutions

    DOE Patents [OSTI]

    Knapp, Furn F. (Oak Ridge, TN); Beets, Arnold L. (Clinton, TN); Mirzadeh, Saed (Knoxville, TN); Guhlke, Stefan (Bonn, DE)

    1998-01-01

    A method of preparing a concentrated solution of a carrier-free radioisotope which includes the steps of: a. providing a generator column loaded with a composition containing a parent radioisotope; b. eluting the generator column with an eluent solution which includes a salt of a weak acid to elute a target daughter radioisotope from the generator column in a first eluate. c. eluting a cation-exchange column with the first eluate to exchange cations of the salt for hydrogen ions and to elute the target daughter radioisotope and a weak acid in a second eluate; d. eluting an anion-exchange column with the second eluate to trap and concentrate the target daughter radioisotope and to elute the weak acid solution therefrom; and e. eluting the concentrated target daughter radioisotope from the anion-exchange column with a saline solution.

  2. Agri Energy Funding Solutions | Open Energy Information

    Open Energy Info (EERE)

    Place: Omaha, Nebraska Zip: 68137-2495 Sector: Biomass, Wind energy Product: AGRI-ENERGY FUNDING SOLUTIONS is a market consultant for BioDiesel, Ethanol as well as Biomass...

  3. E3 Regenesis Solutions | Open Energy Information

    Open Energy Info (EERE)

    Foster City, California Zip: 94404 Product: A California-based company developing waste-to-energy projects in the southern US. References: E3 Regenesis Solutions1 This article...

  4. EIS-0219: F-Canyon Plutonium Solutions

    Broader source: Energy.gov [DOE]

    This EIS evaluates the potential environmental impacts of processingthe plutonium solutions to metal form using the F-Canyon and FB-Line facilities at the Savannah River Site.

  5. IID Energy- PV Solutions Rebate Program

    Broader source: Energy.gov [DOE]

    IID accepted applications for the 2015 PV Solutions Program from Jan. 3, 2015 – Jan. 31, 2015. Winners were determined via lottery. The program is now closed for the remainder of 2015, but another...

  6. SolSolution | Open Energy Information

    Open Energy Info (EERE)

    Boston Area Sector: Solar Year Founded: 2007 Phone Number: 805-813-4418 Website: www.sol-solution.org Coordinates: 42.363951, -71.10122 Show Map Loading map......

  7. Removal of metal ions from aqueous solution

    DOE Patents [OSTI]

    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)

    1990-11-13

    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.

  8. Removal of metal ions from aqueous solution

    DOE Patents [OSTI]

    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)

    1990-01-01

    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.

  9. Prime BioSolutions | Open Energy Information

    Open Energy Info (EERE)

    search Name: Prime BioSolutions Place: Omaha, Nebraska Zip: 68137 Product: Ethanol and biogas producer using the closed-loop system. Coordinates: 33.180954, -94.743294 Show Map...

  10. Missing solution in a Cornell potential

    SciTech Connect (OSTI)

    Castro, L.B.; Castro, A.S. de

    2013-11-15

    Missing bound-state solutions for fermions in the background of a Cornell potential consisting of a mixed scalarvectorpseudoscalar coupling is examined. Charge-conjugation operation, degeneracy and localization are discussed. -- Highlights: The Dirac equation with scalarvectorpseudoscalar Cornell potential is investigated. The isolated solution from the SturmLiouville problem is found. Charge-conjugation operation, degeneracy and localization are discussed.

  11. SEPARATION OF SCANDIUM FROM AQUEOUS SOLUTIONS

    DOE Patents [OSTI]

    Peppard, D.F.; Nachtman, E.S.

    1958-02-25

    This patent relates to a process for the separation of scandium from yttrium, thorium, and trivalent rare earths and with their separation from each other. It has been found that scandium and yttrium can be separated from trivalent rare earths in acidic solution, for example, a solution 6 M in HCl, by contacting with tributyl phosphate, whereupon the scandum is preferentially extracted into the organic phase, leaving the yttrium and trivalent rare earths in the aqueous phase.

  12. Solution dewatering with concomitant ion removal

    DOE Patents [OSTI]

    Peterson, Eric S.; Marshall, Douglas W.; Stone, Mark L.

    2003-08-05

    One of the biggest needs in the separations and waste handling and reduction area is a method for dewatering ion-containing solutions. Unexpectedly, it has been found that phosphazene polymers can discriminate between water and metal ions, allowing water to pass through the membrane while retaining the ions. This unexpected result, along with the inherent chemical and thermal stability of the phosphazene polymers, yields a powerful tool for separating and dewatering metal-ion-containing solutions.

  13. Marchetti New CEO of Washington TRU Solutions

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

    For Immediate Release Marchetti New CEO of Washington TRU Solutions CARLSBAD, N.M., July 31, 2003 - Stephen Marchetti, Executive Vice President of Operations for the Energy and Environment unit of Washington Group International, has been chosen to replace Pres Rahe as Chairman and CEO of Washington TRU Solutions LLC (WTS). WTS, the prime contractor for the U.S. Department of Energy (DOE) at the Waste Isolation Pilot Plant (WIPP) near Carlsbad, NM, is responsible for cleanup and disposal of the

  14. Better Buildings Residential Program Solution Center Demonstration

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

    Webinar Better Buildings Residential Program Solution Center Demonstration Amanda Chiu: My name is Amanda Chiu, and I'm with Energetics, Incorporated, on behalf of the U.S. Department of Energy (DOE) Better Buildings Residential Program. Thank you for joining us today, and welcome to a demonstration of the Better Buildings Residential Program's Solution Center. We have with us today Danielle Byrnett with the U.S. Department of Energy. Danielle is the supervisor for the Better Buildings

  15. GSA Solutions for Federally Recognized Tribes

    Office of Environmental Management (EM)

    Service U.S. General Services Administration GSA Solutions for Federally- Recognized Tribes Federal Acquisition Service U.S. General Services Administration 2 Overview  Customer Service Office Alaska  Support to Federally-Recognized Tribes  Additional Resources  Questions Federal Acquisition Service U.S. General Services Administration 3 GSA - Our Mission GSA's mission is to use expertise to provide innovative solutions for our customers in support of their missions and by so doing

  16. Sodium Hydroxide Extraction From Caustic Leaching Solutions

    SciTech Connect (OSTI)

    Lumetta, Gregg J.; Garza, Priscilla A.; Levitskaia, Tatiana G.; Brown, Gilbert M.

    2002-09-18

    This report describes experiments conducted to demonstrate the proof-of-principle of a method to recover NaOH from Hanford tank sludge leaching solutions. Aqueous solutions generated from leaching actual Hanford tank waste solids were used. The process involves neutralization of a lipophilic weak acid (t-octylphenol was used in these experiments) by reaction with NaOH in the aqueous phase. This results in the transfer of Na into the organic phase. Contacting with water reverses this process, reprotonating the lipophilic weak acid and transferring Na back into the aqueous phase as NaOH. The work described here confirms the potential application of solvent extraction to recover and recycle NaOH from solutions generated by leaching Hanford tank sludges. Solutions obtained by leaching sludges from tanks S-110 and T-110 were used in this work. It was demonstrated that Na+ is transferred from caustic leaching solution to the organic phase when contacted with t-octylphenol solutions. This was accompanied by a concomitant decrease in the aqueous-phase hydroxide ion concentration. Seventy to 80 % of the extracted Na was recovered by 3 to 4 sequential contacts of the organic phase with water. Cesium was co-extracted by the procedure, but Al and Cr remained in the feed stream.

  17. Deep subsurface drip irrigation using coal-bed sodic water: Part I. Water and solute movement

    SciTech Connect (OSTI)

    Bern, Carleton R.; Breit, George N.; Healy, Richard W.; Zupancic, John W.; Hammack, Richard

    2013-02-01

    Water co-produced with coal-bed methane (CBM) in the semi-arid Powder River Basin of Wyoming and Montana commonly has relatively low salinity and high sodium adsorption ratios that can degrade soil permeability where used for irrigation. Nevertheless, a desire to derive beneficial use from the water and a need to dispose of large volumes of it have motivated the design of a deep subsurface drip irrigation (SDI) system capable of utilizing that water. Drip tubing is buried 92 cm deep and irrigates at a relatively constant rate year-round, while evapotranspiration by the alfalfa and grass crops grown is seasonal. We use field data from two sites and computer simulations of unsaturated flow to understand water and solute movements in the SDI fields. Combined irrigation and precipitation exceed potential evapotranspiration by 300480 mm annually. Initially, excess water contributes to increased storage in the unsaturated zone, and then drainage causes cyclical rises in the water table beneath the fields. Native chloride and nitrate below 200 cm depth are leached by the drainage. Some CBM water moves upward from the drip tubing, drawn by drier conditions above. Chloride from CBM water accumulates there as root uptake removes the water. Year over year accumulations indicated by computer simulations illustrate that infiltration of precipitation water from the surface only partially leaches such accumulations away. Field data show that 7% and 27% of added chloride has accumulated above the drip tubing in an alfalfa and grass field, respectively, following 6 years of irrigation. Maximum chloride concentrations in the alfalfa field are around 45 cm depth but reach the surface in parts of the grass field, illustrating differences driven by crop physiology. Deep SDI offers a means of utilizing marginal quality irrigation waters and managing the accumulation of their associated solutes in the crop rooting zone.

  18. Ion Recognition Approach to Volume Reduction of Alkaline Tank Waste by Separation and Recycle of Sodium Hydroxide and Sodium Nitrate

    SciTech Connect (OSTI)

    Moyer, Bruce A.; Marchand, Alan P.

    2001-06-01

    Disposal of high-level nuclear waste is horrendously expensive, in large part because the actual radioactive matter in the tanks has been diluted over 1000-fold by ordinary inorganic chemicals. Treatment processes themselves can exacerbate the problem by adding further volume to the waste. Waste retrieval and sludge washing, for example, will require copious amounts of sodium hydroxide. If the needed sodium hydroxide could be separated from the waste and recycled, however, the addition of fresh sodium hydroxide could be avoided, ultimately reducing the final waste volume and associated disposal costs. The major objective of this research is to explore new liquid-liquid extraction approaches to the selective separation of sodium hydroxide from alkaline high-level wastes stored in underground tanks at the Hanford and Savannah River sites. Consideration is also given to separating potassium and abundant anions, including nitrate, nitrite, aluminate, and carbonate. Salts of these ions represent possible additional value for recycle, alternative disposal, or even use as commodity chemicals. A comprehensive approach toward understanding the extractive chemistry of these salts is envisioned, involving systems of varying complexity, from use of simple solvents to new bifunctional host molecules for ion-pair recognition. These extractants will ideally require no adjustment of the waste composition and will release the extracted salt into water, thereby consuming no additional chemicals and producing no additional waste volume. The overall goal of this research is to provide a scientific foundation upon which the feasibility of new liquid-liquid extraction chemistry applicable to the bulk reduction of the volume of tank waste can be evaluated.

  19. Ion Recognition Approach to Volume Reduction of Alkaline Tank Waste by Separation and Recycle of Sodium Hydroxide and Sodium Nitrate

    SciTech Connect (OSTI)

    Moyer, Bruce A.; Marchand, Alan P.

    2000-06-01

    Disposal of high- level waste is horrendously expensive, in large part because the actual radioactive matter in the tanks has been diluted over 1000-fold by ordinary inorganic chemicals. Treatment processes themselves can exacerbate the problem by adding further volume to the waste. Waste retrieval and sludge washing, for example, will require copious amounts of sodium hydroxide. If the needed sodium hydroxide could be separated from the waste and recycled, however, the addition of fresh sodium hydroxide could be avoided, ultimately reducing the final waste volume and associated disposal costs. The major objective of this research is to explore new liquid- liquid extraction approaches to the selective separation of sodium hydroxide from alkaline high-level wastes stored in underground tanks at the Hanford and Savannah River sites. Consideration is also given to separating potassium and abundant anions, including nitrate, nitrite, aluminate, and carbonate. Salts of these ions represent possible additional value for recycle, alternative disposal, or even use as commodity chemicals. A comprehensive approach toward understanding the extractive chemistry of these salts is envisioned, involving systems of varying complexity, from use of simple solvents to new bifunctional host molecules for ion-pair recognition. These extractants will ideally require no adjustment of the waste composition and will release the extracted salt into water, thereby consuming no additional chemicals and producing no additional waste volume. The overall goal of this research is to provide a scientific foundation upon which the feasibility of new liquid-liquid extraction chemistry applicable to the bulk reduction of the volume of tank waste can be evaluated.

  20. Ion Recognition Approach to Volume Reduction of Alkaline Tank Waste by Separation and Recycle of Sodium Hydroxide and Sodium Nitrate

    SciTech Connect (OSTI)

    Moyer, Bruce A.; Marchand, Alan P.; Bryan, Jeffrey C.; Bonnesen, Peter V.

    1999-06-01

    The objective of this research is to explore new liquid-liquid extraction approaches to the selective separation of major sodium salts from alkaline high-level wastes stored in underground tanks at Hanford, Savannah River, and Oak Ridge sites. Disposal of high level waste is horrendously expensive, in large part because the actual radioactive matter in the tanks has been diluted over 1000-fold by ordinary inorganic chemicals. Since the residual bulk chemicals must still undergo expensive treatment and disposal after most of the hazardous radionuclides have been removed, large cost savings will result from processes that reduce the overall waste volume. It is proposed that major cost savings can be expected if sodium hydroxide needed for sludge washing can be obtained from the waste itself, thus avoiding the addition of yet another bulk chemical to the waste and still further increase of the waste volume and disposal cost. Secondary priority is given to separating potassium an d abundant anions, including nitrate, nitrite, aluminate, and carbonate. Salts of these ions represent possible additional value for recycle, alternative disposal, or even use as commodity chemicals. A comprehensive approach toward understanding the extractive chemistry of these salts is envisioned, involving systems of varying complexity, from use of simple solvents to new bifunctional host molecules for ion-pair recognition. These extractants will ideally require no adjustment of the waste composition and will release the extracted salt into water, thereby consuming no additional chemicals and producing no additional waste volume. The overall goal of this research is to provide a scientific foundation upon which the feasibility of new liquid-liquid extraction chemistry applicable to the bulk reduction of the volume of tank waste can be evaluated.

  1. Clean Energy Solutions Centers Fact Sheet | Department of Energy

    Office of Environmental Management (EM)

    Clean Energy Solutions Centers Fact Sheet Clean Energy Solutions Centers Fact Sheet A fact sheet describing the mission of the Clean Energy Solution Center. PDF icon Clean Energy Solutions Centers Fact Sheet More Documents & Publications Clean-Energy-Solutions-Centers-Fact-Sheet.pdf Clean Energy Ministerial Press Fact Sheet SLED-Fact-Sheet.pdf

  2. Cadmium zinc sulfide by solution growth

    DOE Patents [OSTI]

    Chen, Wen S.

    1992-05-12

    A process for depositing thin layers of a II-VI compound cadmium zinc sulfide (CdZnS) by an aqueous solution growth technique with quality suitable for high efficiency photovoltaic or other devices which can benefit from the band edge shift resulting from the inclusion of Zn in the sulfide. A first solution comprising CdCl.sub.2 2.5H.sub.2 O, NH.sub.4 Cl, NH.sub.4 OH and ZnCl.sub.2, and a second solution comprising thiourea ((NH.sub.2).sub.2 CS) are combined and placed in a deposition cell, along with a substrate to form a thin i.e. 10 nm film of CdZnS on the substrate. This process can be sequentially repeated with to achieve deposition of independent multiple layers having different Zn concentrations.

  3. Analytical solutions to matrix diffusion problems

    SciTech Connect (OSTI)

    Keklinen, Pekka

    2014-10-06

    We report an analytical method to solve in a few cases of practical interest the equations which have traditionally been proposed for the matrix diffusion problem. In matrix diffusion, elements dissolved in ground water can penetrate the porous rock surronuding the advective flow paths. In the context of radioactive waste repositories this phenomenon provides a mechanism by which the area of rock surface in contact with advecting elements is greatly enhanced, and can thus be an important delay mechanism. The cases solved are relevant for laboratory as well for in situ experiments. Solutions are given as integral representations well suited for easy numerical solution.

  4. ENDF/B-VII.0, ENDF/B-VI, JEFF-3.1, AND JENDL-3.3 RESULTS FOR UNREFLECTED PLUTONIUM SOLUTIONS AND MOX LATTICES (U)

    SciTech Connect (OSTI)

    MOSTELLER, RUSSELL D.

    2007-02-09

    Previous studies have indicated that ENDF/B-VII preliminary releases {beta}-2 and {beta}-3, predecessors to the recent initial release of ENDF/B-VII.0, produce significantly better overall agreement with criticality benchmarks than does ENDF/B-VI. However, one of those studies also suggests that improvements still may be needed for thermal plutonium cross sections. The current study substantiates that concern by examining criticality benchmarks for unreflected spheres of plutonium-nitrate solutions and for slightly and heavily borated mixed-oxide (MOX) lattices. Results are presented for the JEFF-3.1 and JENDL-3.3 nuclear data libraries as well as ENDF/B-VII.0 and ENDF/B-VI. It is shown that ENDF/B-VII.0 tends to overpredict reactivity for thermal plutonium benchmarks over at least a portion of the thermal range. In addition, it is found that additional benchmark data are needed for the deep thermal range.

  5. Transition between vortex rings and MAP solutions for electrically charged magnetic solutions

    SciTech Connect (OSTI)

    Wong, Khai-Ming; Soltanian, Amin; Teh, Rosy

    2014-03-05

    We consider the bifurcation and transition of axially symmetric monopole-antimonopole pair (MAP) and vortex ring solutions in the presence of electric charge for the SU(2) Yang-Mills-Higgs field theory. Here we investigate the properties of MAP/vortex ring solutions with n = 3,? = 0.65, for different Higgs field strength ?. For ? < 4.93, there is only one fundamental branch of vortex ring solution, but at the critical value of ?{sub b} = 4.93, branching happens and 2 sets of new solutions appeared. The new branch with less energy is a full MAP solution while the branch with higher energy contains MAP at the beginning and separation between poles of MAP on the z-axis reduces gradually and at another critical value of ?{sub t} = 14.852, they merge together at z = 0. Beyond this point the solutions change to the vortex ring solutions and a transitions between MAP and vortex ring solutions happens at this branch.

  6. Nitrative DNA damage induced by multi-walled carbon nanotube via endocytosis in human lung epithelial cells

    SciTech Connect (OSTI)

    Guo, Feiye; Ma, Ning; Horibe, Yoshiteru; Kawanishi, Shosuke; Murata, Mariko; Hiraku, Yusuke

    2012-04-15

    Carbon nanotube (CNT) has a promising usage in the field of material science for industrial purposes because of its unique physicochemical property. However, intraperitoneal administration of CNT was reported to cause mesothelioma in experimental animals. Chronic inflammation may contribute to carcinogenesis induced by fibrous materials. 8-Nitroguanine is a mutagenic DNA lesion formed during inflammation and may play a role in CNT-induced carcinogenesis. In this study, we examined 8-nitroguanine formation in A549 human lung alveolar epithelial cells treated with multi-walled CNT (MWCNT) by fluorescent immunocytochemistry. Both MWCNTs with diameter of 2030 nm (CNT20) and 4070 nm (CNT40) significantly induced 8-nitroguanine formation at 5 and 10 ?g/ml (p < 0.05), which persisted for 24 h, although there was no significant difference in DNA-damaging abilities of these MWCNTs. MWCNTs significantly induced the expression of inducible nitric oxide synthase (iNOS) for 24 h (p < 0.05). MWCNTs also significantly increased the level of nitrite, a hydrolysis product of oxidized NO, in the culture supernatant at 4 and 8 h (p < 0.05). MWCNT-induced 8-nitroguanine formation and iNOS expression were largely suppressed by inhibitors of iNOS (1400 W), nuclear factor-?B (Bay11-7082), actin polymerization (cytochalasin D), caveolae-mediated endocytosis (methyl-?-cyclodextrin, MBCD) and clathrin-mediated endocytosis (monodansylcadaverine, MDC). Electron microscopy revealed that MWCNT was mainly located in vesicular structures in the cytoplasm, and its cellular internalization was reduced by MBCD and MDC. These results suggest that MWCNT is internalized into cells via clathrin- and caveolae-mediated endocytosis, leading to inflammatory reactions including iNOS expression and resulting nitrative DNA damage, which may contribute to carcinogenesis. Highlights: ?Multi-walled carbon nanotube (MWCNT) caused DNA damage in A549 cells. ?MWCNT formed 8-nitroguanine, a DNA lesion associated with inflammatory response. ?MWCNT was internalized into cells via caveolin- and clathrin-mediated endocytosis. ?8-Nitroguanine formation and iNOS expression involved these types of endocytosis. ?Internalized MWCNT plays a key role in inflammatory response and DNA damage.

  7. First Energy Solutions Corp. (New Jersey) | Open Energy Information

    Open Energy Info (EERE)

    Solutions Corp. Name: First Energy Solutions Corp. Abbreviation: FES Address: 341 White Pond Dr., Building B3 Place: Akron, Ohio Country: United States Zip: 44320 Service...

  8. One Acquisition Solution for Integrated Services (OASIS) - Brad...

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

    Acquisition Solution for Integrated Services (OASIS) - Brad DeMers, General Services Administration (GSA) One Acquisition Solution for Integrated Services (OASIS) - Brad DeMers,...

  9. 2015 Tribal Energy Summit to Explore Solutions to Energy and...

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

    2015 Tribal Energy Summit to Explore Solutions to Energy and Climate Challenges 2015 Tribal Energy Summit to Explore Solutions to Energy and Climate Challenges September 11, 2015 -...

  10. Building America Technology Solutions for New and Existing Homes...

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

    Building America Technology Solutions for New and Existing Homes: Low-Load Space-Conditioning Needs Assessment, Northeast and Mid-Atlantic Building America Technology Solutions for...

  11. Building America Technology Solutions for New and Existing Homes...

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

    Building America Technology Solutions for New and Existing Homes: Investigating Solutions to Wind Washing Issues in Two-Story Florida Homes: Phase 2, Southeastern United States...

  12. Wniwick Business Solutions P/L | Open Energy Information

    Open Energy Info (EERE)

    Wniwick Business Solutions PL Jump to: navigation, search Name: Wniwick Business Solutions PL Address: 739 Mount Macedon Road Place: Mount Macedon, Australia Number of Employees:...

  13. Scientists propose a solution to a critical barrier to producing...

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

    Scientists propose a solution to a critical barrier to producing fusion By John Greenwald ... solution to a mystery that has long baffled researchers working to harness fusion. ...

  14. Solar Systems and Solutions Soluciones Sistemas Solares 3S |...

    Open Energy Info (EERE)

    Systems and Solutions Soluciones Sistemas Solares 3S Jump to: navigation, search Name: Solar Systems and Solutions Soluciones Sistemas Solares (3S) Place: Navarre, Spain Sector:...

  15. Apply: Funding Opportunity - Advancing Solutions to Improve Energy...

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

    Advancing Solutions to Improve Energy Efficiency of Commercial Buildings Apply: Funding Opportunity - Advancing Solutions to Improve Energy Efficiency of Commercial Buildings ...

  16. Integrated Design: A High-Performance Solution for Affordable...

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

    Integrated Design: A High-Performance Solution for Affordable Housing Integrated Design: A High-Performance Solution for Affordable Housing ARIES lab houses. Photo courtesy of The ...

  17. Device for isolation of seed crystals during processing of solution

    DOE Patents [OSTI]

    Montgomery, Kenneth E. (Tracy, CA); Zaitseva, Natalia P. (Livermore, CA); Deyoreo, James J. (Livermore, CA); Vital, Russell L. (Tracy, CA)

    1999-01-01

    A device for isolation of see crystals during processing of solutions. The device enables a seed crystal to be introduced into the solution without exposing the solution to contaminants or to sources of drying and cooling. The device constitutes a seed protector which allows the seed to be present in the growth solution during filtration and overheating operations while at the same time preventing the seed from being dissolved by the under saturated solution. When the solution processing has been completed and the solution cooled to near the saturation point, the seed protector is opened, exposing the seed to the solution and allowing growth to begin.

  18. Building America Whole-House Solutions for New Homes: Winchester...

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

    Building America Whole-House Solutions for New Homes: Winchester Homes and Camberly Homes - Silver Spring, Maryland (Fact Sheet) Building America Whole-House Solutions for New ...

  19. Building America Whole-House Solutions for New Homes: Winchester...

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

    Whole-House Solutions for New Homes: Winchester Homes and Camberley Homes Building America Whole-House Solutions for New Homes: Winchester Homes and Camberley Homes In this ...

  20. Building America Technology Solutions for New and Existing Homes...

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

    Investigating Solutions to Wind Washing Issues in Two-Story Florida Homes: Phase 2, Southeastern United States Building America Technology Solutions for New and Existing Homes: ...

  1. Thermal Product Solutions aka Kayex | Open Energy Information

    Open Energy Info (EERE)

    Product Solutions aka Kayex Jump to: navigation, search Name: Thermal Product Solutions (aka Kayex) Place: Rochester, New York Zip: 14624 Product: Makes industrial ovens and...

  2. Building America Efficient Solutions for Existing Homes Case...

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

    Efficient Solutions for Existing Homes Case Study: Habitat for Humanity of Palm Beach County, Lake Worth, Florida Building America Efficient Solutions for Existing Homes Case ...

  3. Whole-House Solutions Case Study: Sunnyvale Marine Climate Deep...

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

    Whole-House Solutions Case Study: Sunnyvale Marine Climate Deep Retrofit Whole-House Solutions Case Study: Sunnyvale Marine Climate Deep Retrofit The Alliance for Residential ...

  4. Technology Solutions Case Study: Overcoming Comfort Issues Due...

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

    Solutions Case Study: Overcoming Comfort Issues Due to Reduced Flow Room Air Mixing Technology Solutions Case Study: Overcoming Comfort Issues Due to Reduced Flow Room Air Mixing ...

  5. PIA - Savannah River Nuclear Solution SRNS ProRad Environment...

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

    SRNS ProRad Environment Management PIA - Savannah River Nuclear Solution SRNS ProRad Environment Management PIA - Savannah River Nuclear Solution SRNS ProRad Environment Management...

  6. BioEnergy Solutions BES | Open Energy Information

    Open Energy Info (EERE)

    Solutions BES Jump to: navigation, search Name: BioEnergy Solutions (BES) Place: Bakersfield, California Zip: 93309 Product: Bakersfield-based firm installing and operating biogas...

  7. Nanocrystal solar cells processed from solution (Patent) | SciTech...

    Office of Scientific and Technical Information (OSTI)

    Nanocrystal solar cells processed from solution Citation Details In-Document Search Title: Nanocrystal solar cells processed from solution A photovoltaic device having a first...

  8. Building America Business Solutions for New Homes: Marketing...

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

    Business Solutions for New Homes: Marketing Zero Energy Homes: Lifestyle Homes, Melbourne, Florida Building America Business Solutions for New Homes: Marketing Zero Energy Homes: ...

  9. Battery Energy Power Solutions Pty Ltd | Open Energy Information

    Open Energy Info (EERE)

    Energy Power Solutions Pty Ltd Jump to: navigation, search Name: Battery Energy Power Solutions Pty Ltd Place: Sydney, New South Wales, Australia Zip: 2165 Product: Sydney-based...

  10. Building America Technology Solutions for New and Existing Homes...

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

    Technology Solutions for New and Existing Homes: Advanced Controls Improve Performance of Combination Space- and Water-Heating Systems Building America Technology Solutions for New ...

  11. DOE Announces Webinars on Marketing and Sales Solutions for Zero...

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

    Marketing and Sales Solutions for Zero Energy Ready Homes, Building Stronger More Efficient Homes, and More DOE Announces Webinars on Marketing and Sales Solutions for Zero Energy...

  12. A Solution Route to Thermoelectric Oxide Nanoparticles - A Sol...

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

    A Solution Route to Thermoelectric Oxide Nanoparticles - A Sol-Gel Process Employing Heterometallic Alkoxides A Solution Route to Thermoelectric Oxide Nanoparticles - A Sol-Gel ...

  13. Emerging Nanoscale Memory Technologies: The Solution to Extreme...

    Office of Scientific and Technical Information (OSTI)

    Emerging Nanoscale Memory Technologies: The Solution to Extreme Scale Problems. Citation Details In-Document Search Title: Emerging Nanoscale Memory Technologies: The Solution to ...

  14. Progressive Lighting And Energy Solutions Inc | Open Energy Informatio...

    Open Energy Info (EERE)

    Progressive Lighting And Energy Solutions Inc Jump to: navigation, search Name: Progressive Lighting And Energy Solutions Inc Place: Tustin, California Zip: 92780 Product:...

  15. H2 Storage Solutions Inc | Open Energy Information

    Open Energy Info (EERE)

    Storage Solutions Inc Jump to: navigation, search Name: H2 Storage Solutions Inc Place: Bellevue, Washington State Zip: 98006 Sector: Hydro, Hydrogen Product: Focus on hydrogen...

  16. Acme Energy Solutions Pvt Ltd | Open Energy Information

    Open Energy Info (EERE)

    Acme Energy Solutions Pvt Ltd Jump to: navigation, search Name: Acme Energy Solutions Pvt Ltd Place: Gurgaon, Haryana, India Zip: 122001 Sector: Solar Product: Gurgaon-based...

  17. UESC Energy Solutions for Federal Agencies | Department of Energy

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

    Energy Solutions for Federal Agencies UESC Energy Solutions for Federal Agencies This presentation includes an overview of UESC strategies and services by Pepco Energy Services....

  18. Energy solutions-Eric Isaacs | Argonne National Laboratory

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

    Energy solutions-Eric Isaacs Share Description Argonne director Eric Isaacs talks about the laboratory's efforts for creating new, clean energy solutions. Topic Energy Energy...

  19. Cree LED Lighting Solutions Formerly LED Lighting Fixtures LLF...

    Open Energy Info (EERE)

    LED Lighting Solutions Formerly LED Lighting Fixtures LLF Jump to: navigation, search Name: Cree LED Lighting Solutions (Formerly LED Lighting Fixtures (LLF)) Place: Morrisville,...

  20. Two Catalyst Formulations - One Solution for NOx After-treatment...

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

    Catalyst Formulations - One Solution for NOx After-treatment Systems Two Catalyst Formulations - One Solution for NOx After-treatment Systems Low-temperature SCR combined with...

  1. Renewable Devices Energy Solutions Ltd | Open Energy Information

    Open Energy Info (EERE)

    Energy Solutions Ltd Jump to: navigation, search Name: Renewable Devices Energy Solutions Ltd Place: Edinburgh, Scotland, United Kingdom Zip: EH26 0PH Sector: Renewable Energy...

  2. Device for isolation of seed crystals during processing of solution

    DOE Patents [OSTI]

    Montgomery, K.E.; Zaitseva, N.P.; Deyoreo, J.J.; Vital, R.L.

    1999-05-18

    A device is described for isolation of seed crystals during processing of solutions. The device enables a seed crystal to be introduced into the solution without exposing the solution to contaminants or to sources of drying and cooling. The device constitutes a seed protector which allows the seed to be present in the growth solution during filtration and overheating operations while at the same time preventing the seed from being dissolved by the under saturated solution. When the solution processing has been completed and the solution cooled to near the saturation point, the seed protector is opened, exposing the seed to the solution and allowing growth to begin. 3 figs.

  3. Environmental Management and Planning Solutions, Inc | Open Energy...

    Open Energy Info (EERE)

    Environmental Management and Planning Solutions, Inc (Redirected from EMPSi) Jump to: navigation, search Name: Environmental Management and Planning Solutions, Inc Abbreviation:...

  4. Emission Power Solutions Plc EPS | Open Energy Information

    Open Energy Info (EERE)

    Power Solutions Plc EPS Jump to: navigation, search Name: Emission & Power Solutions Plc (EPS) Place: Carlsbad, California Zip: 92008 Sector: Efficiency Product: California-based...

  5. Building America Solution Center - Building America Top Innovation...

    Energy Savers [EERE]

    Building America Solution Center - Building America Top Innovation SCimagemale.jpg The Building America Solution Center is a Web-based tool connecting users to fast, free, and ...

  6. Remarks on Grid Generation Equidistribution and Solution-Adaptation...

    Office of Scientific and Technical Information (OSTI)

    Remarks on Grid Generation Equidistribution and Solution-Adaptation. Citation Details In-Document Search Title: Remarks on Grid Generation Equidistribution and Solution-Adaptation....

  7. Encapsulant-based Solution to Potential Induced Degradation of...

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

    Encapsulant-based Solution to Potential Induced Degradation of Photovoltaic Modules Encapsulant-based Solution to Potential Induced Degradation of Photovoltaic Modules Presented at ...

  8. 21st century Green Solutions LLC | Open Energy Information

    Open Energy Info (EERE)

    21st century Green Solutions LLC Jump to: navigation, search Name: 21st century Green Solutions, LLC Place: Grand Blanc, Michigan Zip: 48439 Sector: Wind energy Product: Exclusive...

  9. Agricultural Waste Solutions Inc AWS | Open Energy Information

    Open Energy Info (EERE)

    Waste Solutions Inc AWS Jump to: navigation, search Name: Agricultural Waste Solutions Inc (AWS) Place: Westlake Village, California Zip: CA 91361 Product: Agricultural Waste...

  10. Applications Solutions Science Predicting Materials Behavior

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

    Applications Solutions Science Predicting Materials Behavior Data Science at Scale Complex Networks Computational Co-Design Situational Awareness Energy Climate Interactions Science that Matters: Integrating Information, Science, and Technology for Prediction Implementation Plan v 3.0 February 2014 LA-UR-14-23474 Table of Contents Executive Summary ............................................................................................................ 1 Program Areas

  11. Observations of solute effects on bubble formation

    SciTech Connect (OSTI)

    Hofmeier, U.; Yaminsky, V.V.; Christenson, H.K.

    1995-09-01

    The authors have studied the effects of solute, in particular aqueous electrolyte, on bubble formation at capillary orifices and frits at varying gas flow rates. Using a stroboscope, video microscope, and rotating mirror, they have obtained pictures which show how bubble formation involves the interaction of bubbles at the orifice. These interactions depend on the value of the surface elasticity E due to positively (ethanol) or negatively (NaCl) adsorbed solute. At low flow rates consecutive bubbles do not interact. Each bubble detaches and leaves the orifice region before the next one starts forming. A intermediate flow rates the more closely spaced, consecutive bubbles begin to interact. In pure liquids there is no barrier to bubble coalescence and the detached bubble is fed by the subsequent bubble as this starts to grow. The process may be repeated several times before the original bubble has risen out of range. In solutions where E is large enough bubble coalescence is inhibited. Instead of feeding into the detached bubble the following bubble pushes it aside, and the bubbles appear to bounce off each other. Bouncing may give rise to a characteristic sequence of larger and smaller bubbles if the emerging bubbles break off prematurely from the orifice due to the inertia of the original bubble. The transition from feeding to bouncing depends critically on E of the solution and leads to a smaller average bubble size for large E values. At high flow rates detached bubbles are invariably fed by several subsequent ones. At very high flow rates the bubbling becomes chaotic, but the interaction of bubbles after leaving the orifice area produces smaller bubbles in solutions. Bouncing is more likely to occur with narrow and irregular capillaries. The dramatically different appearance of gas-sparged columns in salt water and freshwater has its origin in the difference between assemblies of pores showing mainly feeding (freshwater) or bouncing (salt water).

  12. Clean Energy Solutions Center Services (Chinese Translation) (Fact Sheet)

    SciTech Connect (OSTI)

    Not Available

    2014-04-01

    This is the Chinese language translation of the Clean Energy Solutions Center (Solutions Center) fact sheet. The Solutions Center helps governments, advisors and analysts create policies and programs that advance the deployment of clean energy technologies. The Solutions Center partners with international organizations to provide online training, expert assistance, and technical resources on clean energy policy.

  13. EA-306-B MAG Energy Solutions, Inc. | Department of Energy

    Energy Savers [EERE]

    -B MAG Energy Solutions, Inc. EA-306-B MAG Energy Solutions, Inc. Order authorizing MAG Energy Solutions (MAG E.S.) to export electric energy to Canada. PDF icon EA-306-B MAG ES (CN).pdf More Documents & Publications EA-306-A MAG Energy Solutions, Inc. EA-388 TEC Energy Inc. EA-257-D Emera Energy Services

  14. Clean Energy Solutions Center Services (Vietnamese Translation) (Fact Sheet)

    SciTech Connect (OSTI)

    Not Available

    2014-11-01

    This is the Vietnamese language translation of the Clean Energy Solutions Center (Solutions Center) fact sheet. The Solutions Center helps governments, advisors and analysts create policies and programs that advance the deployment of clean energy technologies. The Solutions Center partners with international organizations to provide online training, expert assistance, and technical resources on clean energy policy.

  15. Clean Energy Solutions Center Services (Arabic Translation) (Fact Sheet)

    SciTech Connect (OSTI)

    Not Available

    2014-06-01

    This is the Arabic translation of the Clean Energy Solutions Center Services fact sheet. The Clean Energy Solutions Center (Solutions Center) helps governments, advisors and analysts create policies and programs that advance the deployment of clean energy technologies. The Solutions Center partners with international organizations to provide online training, expert assistance, and technical resources on clean energy policy.

  16. Better Buildings Residential Program Solution Center Demonstration Webinar

    Broader source: Energy.gov [DOE]

    Demonstration webinar slides for Better Buildings Residential Program Solution Center, November 19, 2014.

  17. PIA - Hiring Management Enterprise Solutions (HMES) | Department of Energy

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

    Hiring Management Enterprise Solutions (HMES) PIA - Hiring Management Enterprise Solutions (HMES) PIA - Hiring Management Enterprise Solutions (HMES) PDF icon PIA - Hiring Management Enterprise Solutions (HMES) More Documents & Publications Integrated Safety Management Workshop Registration, PIA, Idaho National Laboratory PIA - WEB Physical Security Major Application PIA - 10th International Nuclear Graphite Specialists Meeting registration web site

  18. The Radiolysis of AmVI Solutions

    SciTech Connect (OSTI)

    Bruce J. Mincher

    2013-06-01

    The reduction of bismuthate-produced AmVI by 60Co gamma-rays was measured using post-irradiation UV/Vis spectroscopy. The reduction of AmVI by radiolysis was rapid, producing AmV as the sole product. Relatively low absorbed doses in the ~0.3 kGy range quantitatively reduced a solution of 2.5 x 10-4 M AmVI. The addition of bismuthate to samples during irradiation did not appear to protect AmVI from radiolytic reduction during these experiments. It was also shown here that AmV is very stable toward radiation. The quantitative reduction of the AmVI concentration here corresponds to 1.4 hours of exposure to a process solution, however the actual americium concentrations will be higher and the expected contact times short when using centrifugal contactors. Thus, the reduction rate found in these initial experiments may not be excessive.

  19. Micellar compositions in mixed surfactant solutions

    SciTech Connect (OSTI)

    Zhi-Jian Yu ); Guo-Xi Zhao )

    1993-03-15

    Micellization of aqueous mixtures of alkyltriethylammonium bromide and sodium alkylsulfate in the presence of excess sodium bromide has been studied by surface tension measurements. The molecular ratio of the cationic surfactant to the anionic surfactant in the mixed micelles is deduced by applying the Gibbs-Duhem equation to the measured critical micelle concentrations. Approximately equimolar amounts of the surfactant components in the mixed micelles over a wide range of aqueous mixing ratio are found in the systems of components similar in chain lengths. Large deviations of the surfactant molecular ratio deduced by the regular solution approach (Rubingh's model) when compared with that deduced by this approach are discovered, which suggests a limitation in applying the regular solution approach to mixed systems of cationic/anionic surfactants.

  20. Dissolution of lead paint in aqueous solutions

    SciTech Connect (OSTI)

    Barnes, G.L.; Davis, A.P.

    1996-07-01

    An analysis of the rate and extent of lead leaching from a lead-based paint was completed. At low-solution pH, dissolution was rapid and approached 80% of the total lead. Residual lead can be estimated based on the predicted solubility of lead carbonate and basic lead carbonate. Release of lead from the paint was slower than that from pure basic lead carbonate due to inhibition by the paint matrix. Although the dissolved concentration of lead in solution at neutral/high pH was low, the paint binder was apparently destroyed at these pH values, releasing colloidal lead pigment particles. The presence of ethylenediaminetetraacetic acid (EDTA) and nitrilotriacetic acid (NTA) enhanced both the rate and degree of lead dissolution, while benzoic acid had a minimal effect.

  1. Adjustable flow rate controller for polymer solutions

    DOE Patents [OSTI]

    Jackson, Kenneth M. (Bartlesville, OK)

    1981-01-01

    An adjustable device for controlling the flow rate of polymer solutions which results in only little shearing of the polymer molecules, said device comprising an inlet manifold, an outlet manifold, a plurality of tubes capable of providing communication between said inlet and outlet manifolds, said tubes each having an internal diameter that is smaller than that of the inlet manifold and large enough to insure that viscosity of the polymer solution passing through each said tube will not be reduced more than about 25 percent, and a valve associated with each tube, said valve being capable of opening or closing communication in that tube between the inlet and outlet manifolds, each said valve when fully open having a diameter that is substantially at least as great as that of the tube with which it is associated.

  2. Solution of structured non-stiff ODEs

    SciTech Connect (OSTI)

    Shampine, L.F.

    1984-11-01

    The solution of the initial value problem for a system of ordinary differential equations (ODEs), y' = f(x,y), by Runge-Kutta methods is considered. The structure to be exploited is that a large portion of the cost of evaluating f(x,y) arises in the evaluation of functions of the independent variable x only. It is shown that when the structure is favorable, there are methods which are considerably more efficient than those currently used in general purpose codes.

  3. Integrating Variable Renewable Energy: Challenges and Solutions

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

    Integrating Variable Renewable Energy: Challenges and Solutions L. Bird, M. Milligan, and D. Lew National Renewable Energy Laboratory Technical Report NREL/TP-6A20-60451 September 2013 NREL is a national laboratory of the U.S. Department of Energy Office of Energy Efficiency & Renewable Energy Operated by the Alliance for Sustainable Energy, LLC This report is available at no cost from the National Renewable Energy Laboratory (NREL) at www.nrel.gov/publications. Contract No.

  4. Alkaline earth cation extraction from acid solution

    DOE Patents [OSTI]

    Dietz, Mark (Elmhurst, IL); Horwitz, E. Philip (Naperville, IL)

    2003-01-01

    An extractant medium for extracting alkaline earth cations from an aqueous acidic sample solution is described as are a method and apparatus for using the same. The separation medium is free of diluent, free-flowing and particulate, and comprises a Crown ether that is a 4,4'(5')[C.sub.4 -C.sub.8 -alkylcyclohexano]18-Crown-6 dispersed on an inert substrate material.

  5. Solution-grown crystals for neutron radiation detectors, and methods of solution growth

    DOE Patents [OSTI]

    Zaitseva, Natalia P.; Hull, Giulia; Cherepy, Nerine J.; Payne, Stephen A.; Stoeffl, Wolfgang

    2012-06-26

    A method according to one embodiment includes growing an organic crystal from solution, the organic crystal exhibiting a signal response signature for neutrons from a radioactive source. A system according to one embodiment includes an organic crystal having physical characteristics of formation from solution, the organic crystal exhibiting a signal response signature for neutrons from a radioactive source; and a photodetector for detecting the signal response of the organic crystal. A method according to another embodiment includes growing an organic crystal from solution, the organic crystal being large enough to exhibit a detectable signal response signature for neutrons from a radioactive source. An organic crystal according to another embodiment includes an organic crystal having physical characteristics of formation from solution, the organic crystal exhibiting a signal response signature for neutrons from a radioactive source, wherein the organic crystal has a length of greater than about 1 mm in one dimension.

  6. Studies on lanthanoid complexes of open chain multidentate ligands. VIII. Preparation and structural characterization of the undecacoordinate complex of neodymium nitrate with N,N{prime}-bis(4-methoxyphenyl)tetraglycollic diamide

    SciTech Connect (OSTI)

    Zhijian Liang; Xinmin Gan; Ning Tang; Minyu Tan; Kaibei Yu; Ganzu Tan

    1993-12-31

    The title compound [Nd(L)(NO{sub 3}){sub 3}]2CH{sub 3}CN was formed by reaction of neodymium nitrate with N,N{prime}-bis(4-methoxyphenyl)tetraglycollic diamide (L). The complex crystallizes in the monoclinic system, space group Cc with Z = 4, a = 21.305(6), b = 11.470(4), c = 14.436(3) {angstrom}, {beta} = 97.41(2), V = 3498(2) {angstrom}{sup 3}. The pentadentate organic ligand wraps around the neodymium ion which is also bonded to three bidentate nitrate groups, achieving uncommon undecacoordination with the following mean bond lengths: Nd-O(etheric), 2.703; Nd-O(carbonyl), 2.518; Nd-O(nitrate), 2.546 {angstrom}. 18 refs., 2 figs., 3 tabs.

  7. Chemical deposition methods using supercritical fluid solutions

    DOE Patents [OSTI]

    Sievers, Robert E. (Boulder, CO); Hansen, Brian N. (Boulder, CO)

    1990-01-01

    A method for depositing a film of a desired material on a substrate comprises dissolving at least one reagent in a supercritical fluid comprising at least one solvent. Either the reagent is capable of reacting with or is a precursor of a compound capable of reacting with the solvent to form the desired product, or at least one additional reagent is included in the supercritical solution and is capable of reacting with or is a precursor of a compound capable of reacting with the first reagent or with a compound derived from the first reagent to form the desired material. The supercritical solution is expanded to produce a vapor or aerosol and a chemical reaction is induced in the vapor or aerosol so that a film of the desired material resulting from the chemical reaction is deposited on the substrate surface. In an alternate embodiment, the supercritical solution containing at least one reagent is expanded to produce a vapor or aerosol which is then mixed with a gas containing at least one additional reagent. A chemical reaction is induced in the resulting mixture so that a film of the desired material is deposited.

  8. Aqueous Solution Vessel Thermal Model Development II

    SciTech Connect (OSTI)

    Buechler, Cynthia Eileen

    2015-10-28

    The work presented in this report is a continuation of the work described in the May 2015 report, Aqueous Solution Vessel Thermal Model Development. This computational fluid dynamics (CFD) model aims to predict the temperature and bubble volume fraction in an aqueous solution of uranium. These values affect the reactivity of the fissile solution, so it is important to be able to calculate them and determine their effects on the reaction. Part A of this report describes some of the parameter comparisons performed on the CFD model using Fluent. Part B describes the coupling of the Fluent model with a Monte-Carlo N-Particle (MCNP) neutron transport model. The fuel tank geometry is the same as it was in the May 2015 report, annular with a thickness-to-height ratio of 0.16. An accelerator-driven neutron source provides the excitation for the reaction, and internal and external water cooling channels remove the heat. The model used in this work incorporates the Eulerian multiphase model with lift, wall lubrication, turbulent dispersion and turbulence interaction. The buoyancy-driven flow is modeled using the Boussinesq approximation, and the flow turbulence is determined using the k-? Shear-Stress-Transport (SST) model. The dispersed turbulence multiphase model is employed to capture the multiphase turbulence effects.

  9. EA-306-A MAG Energy Solutions, Inc. | Department of Energy

    Energy Savers [EERE]

    -A MAG Energy Solutions, Inc. EA-306-A MAG Energy Solutions, Inc. Order authorizing MAG Energy Solutions to export electric energy to Canada. PDF icon EA-306-A MAG ES CN.pdf More Documents & Publications EA-306-B MAG Energy Solutions, Inc. Application to Export Electric Energy OE Docket No. EA-306-A MAG Energy Solutions, Inc. EA-264-C ENMAX Energy Marketing

  10. State and Local Solution Center Contacts | Department of Energy

    Energy Savers [EERE]

    About the State & Local Solution Center » State and Local Solution Center Contacts State and Local Solution Center Contacts Please contact us by email or via postal delivery at: U.S. Department of Energy Energy Efficiency and Renewable Energy 1000 Independence Ave, SW, Mail Stop EE-2K U.S. Department of Energy Washington, DC 20585 State & Local Solution Center Home About the State & Local Solution Center Contact Us

  11. PIA - Savannah River Nuclear Solution (SRNS) Procurement Cycle System (PCS)

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

    | Department of Energy Procurement Cycle System (PCS) PIA - Savannah River Nuclear Solution (SRNS) Procurement Cycle System (PCS) PIA - Savannah River Nuclear Solution (SRNS) Procurement Cycle System (PCS) PDF icon PIA - Savannah River Nuclear Solution (SRNS) Procurement Cycle System (PCS) More Documents & Publications PIA - Savannah River Nuclear Solutions (SRNS) Human Resource Management System (HRMS) PIA - Savannah River Nuclear Solution (SRNS) MedGate Occupational Health and Safety

  12. Fiber optic detector and method for using same for detecting chemical species

    DOE Patents [OSTI]

    Baylor, Lewis C. (North Augusta, SC); Buchanan, Bruce R. (Perkiomenville, PA)

    1995-01-01

    An optical sensing device for uranyl and other substances, a method for making an optical sensing device and a method for chemically binding uranyl and other indicators to glass, quartz, cellulose and similar substrates. The indicator, such as arsenazo III, is immobilized on the substrate using a chemical binding process. The immobilized arsenazo III causes uranyl from a fluid sample to bind irreversibly to the substrate at its active sites, thus causing absorption of a portion of light transmitted through the substrate. Determination of the amount of light absorbed, using conventional means, yields the concentration of uranyl present in the sample fluid. The binding of uranyl on the substrate can be reversed by subsequent exposure of the substrate to a solution of 2,6-pyridinedicarboxylic acid. The chemical binding process is suitable for similarly binding other indicators, such as bromocresol green.

  13. Integrating Variable Renewable Energy: Challenges and Solutions

    SciTech Connect (OSTI)

    Bird, L.; Milligan, M.; Lew, D.

    2013-09-01

    In the U.S., a number of utilities are adopting higher penetrations of renewables, driven in part by state policies. While power systems have been designed to handle the variable nature of loads, the additional supply-side variability and uncertainty can pose new challenges for utilities and system operators. However, a variety of operational and technical solutions exist to help integrate higher penetrations of wind and solar generation. This paper explores renewable energy integration challenges and mitigation strategies that have been implemented in the U.S. and internationally, including forecasting, demand response, flexible generation, larger balancing areas or balancing area cooperation, and operational practices such as fast scheduling and dispatch.

  14. Commercial Lighting Solutions, Webtool Peer Review Report

    SciTech Connect (OSTI)

    Jones, Carol C.; Meyer, Tracy A.

    2009-06-17

    The Commercial Lighting Solutions (CLS) project directly supports the U.S. Department of Energys Commercial Building Energy Alliance efforts to design high performance buildings. CLS creates energy efficient best practice lighting designs for widespread use, and they are made available to users via an interactive webtool that both educates and guides the end user through the application of the Lighting Solutions. This report summarizes the peer review of the beta version of the CLS webtool, which contains retail box lighting solutions. The methodology for the peer review process included data collection (stakeholder input), analysis of the comments, and organization of the input into categories for prioritization of the comments against a set of criteria. Based on this process, recommendations were developed about which feedback should be addressed for the release of version 1.0 of the webtool at the Lightfair conference in New York City in May 2009. Due to the volume of data (~500 comments) the methodology for addressing the peer review comments was central to the success of the ultimate goal of improving the tool. The comments were first imported into a master spreadsheet, and then grouped and organized in several layers. Solutions to each comment were then rated by importance and feasibility to determine the practicality of resolving the concerns of the commenter in the short-term or long-term. The rating system was used as an analytical tool, but the results were viewed thoughtfully to ensure that they were not the sole the factor in determining which comments were recommended for near-term resolution. The report provides a list of the top ten most significant and relevant improvements that will be made within the webtool for version 1.0 as well as appendices containing the short-term priorities in additional detail. Peer review comments that are considered high priority by the reviewers and the CLS team but cannot be completed for Version 1.0 are listed as long-term recommendations.

  15. FISSION PRODUCT REMOVAL FROM ORGANIC SOLUTIONS

    DOE Patents [OSTI]

    Moore, R.H.

    1960-05-10

    The decontamination of organic solvents from fission products and in particular the treatment of solvents that were used for the extraction of uranium and/or plutonium from aqueous acid solutions of neutron-irradiated uranium are treated. The process broadly comprises heating manganese carbonate in air to a temperature of between 300 and 500 deg C whereby manganese dioxide is formed; mixing the manganese dioxide with the fission product-containing organic solvent to be treated whereby the fission products are precipitated on the manganese dioxide; and separating the fission product-containing manganese dioxide from the solvent.

  16. Sustainable Solutions to Global Energy Challenges

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

    Solutions to Global Energy Challenges Carl Wolf Business Development Manager US Department of Energy, Biomass 2013 Washington, DC August 1, 2013 Company Profile  Founded in January 2005  Corporate Headquarters in Chicago, IL, R&D in New Zealand, Operations and BD office in China and India  Funding - Series A: Khosla Ventures - $US 12M in 2007 - Series B: Qiming Ventures - $US 18M in 2010 - Series C: Burrill MLSF - $US 60M in 2012 equity, $US 15M debt WTI  Team CEO: Dr. Jennifer

  17. Cosmic strings: A problem or a solution

    SciTech Connect (OSTI)

    Bennett, D.P.; Bouchet, F.R.

    1987-10-01

    The most fundamental issue in the theory of cosmic strings is addressed by means of Numerical Simulations: the existence of a scaling solution. The resolution of this question will determine whether cosmic strings can form the basis of an attractive theory of galaxy formation or prove to be a cosmological disaster like magnetic monopoles or domain walls. After a brief discussion of our numerical technique, results are presented which, though still preliminary, offer the best support to date of this scaling hypothesis. 6 refs., 2 figs.

  18. Mr. Todd Sellmer Washington TRU Solutions LLC

    National Nuclear Security Administration (NNSA)

    '<uCL.EAR REGULATORY COMM!S.s;O'- 'NA3H1NGTON :::: C 20555-C0i!' August C' 2009 Mr. Todd Sellmer Washington TRU Solutions LLC P.O Box 2078 Carlsbad. NM 88221 SUBJECT CERTIFICATE OF COMPLIANCE NO 9218 FOR THE MODEL NO TRUPACT- " PACKAGE Dear Mr Sellmer' As requested by your application on behalf of the Department of Energy (DOE) dated July 2 ~ 2009. enclosed is Certificate of Compliance No. 9218. RevIsion No. 20, for the Model No TRUPACT-II package. Changes made to the enclosed

  19. Solution-grown crystals for neutron radiation detectors, and methods of solution growth

    DOE Patents [OSTI]

    Zaitseva, Natalia; Carman, M Leslie; Payne, Steve

    2014-10-28

    An organic crystal according to one embodiment includes an organic crystal comprising diphenylacetylene and stilbene or a stilbene derivative, the crystal having physical characteristics of formation from solution, the organic crystal exhibiting a signal response signature for neutrons from a radioactive source. A system according to one embodiment includes an organic crystal comprising diphenylacetylene and stilbene or a stilbene derivative, the crystal having physical characteristics of formation from solution, the organic crystal exhibiting a signal response signature for neutrons from a radioactive source; and a photodetector for detecting the signal response of the organic crystal. Methods of making such crystals are also provided.

  20. Ion aggregation in high salt solutions. III. Computational vibrational spectroscopy of HDO in aqueous salt solutions

    SciTech Connect (OSTI)

    Choi, Jun-Ho; Lim, Sohee; Chon, Bonghwan; Cho, Minhaeng; Kim, Heejae; Kim, Seongheun

    2015-05-28

    The vibrational frequency, frequency fluctuation dynamics, and transition dipole moment of the OD stretch mode of HDO molecule in aqueous solutions are strongly dependent on its local electrostatic environment and hydrogen-bond network structure. Therefore, the time-resolved vibrational spectroscopy the OD stretch mode has been particularly used to investigate specific ion effects on water structure. Despite prolonged efforts to understand the interplay of OD vibrational dynamics with local water hydrogen-bond network and ion aggregate structures in high salt solutions, still there exists a gap between theory and experiment due to a lack of quantitative model for accurately describing OD stretch frequency in high salt solutions. To fill this gap, we have performed numerical simulations of Raman scattering and IR absorption spectra of the OD stretch mode of HDO in highly concentrated NaCl and KSCN solutions and compared them with experimental results. Carrying out extensive quantum chemistry calculations on not only water clusters but also ion-water clusters, we first developed a distributed vibrational solvatochromic charge model for the OD stretch mode in aqueous salt solutions. Furthermore, the non-Condon effect on the vibrational transition dipole moment of the OD stretch mode was fully taken into consideration with the charge response kernel that is non-local polarizability density. From the fluctuating OD stretch mode frequencies and transition dipole vectors obtained from the molecular dynamics simulations, the OD stretch Raman scattering and IR absorption spectra of HDO in salt solutions could be calculated. The polarization effect on the transition dipole vector of the OD stretch mode is shown to be important and the asymmetric line shapes of the OD stretch Raman scattering and IR absorption spectra of HDO especially in highly concentrated NaCl and KSCN solutions are in quantitative agreement with experimental results. We anticipate that this computational approach will be of critical use in interpreting linear and nonlinear vibrational spectroscopies of HDO molecule that is considered as an excellent local probe for monitoring local electrostatic and hydrogen-bonding environment in not just salt but also other confined and crowded solutions.

  1. Allianz Climate Solutions ACS GmbH | Open Energy Information

    Open Energy Info (EERE)

    Allianz Climate Solutions ACS GmbH Jump to: navigation, search Name: Allianz Climate Solutions (ACS) GmbH Place: Munich, Germany Zip: 80802 Product: Munich-based subsidiary of...

  2. Buildng America Whole-House Solutions for New Homes: William...

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

    Buildng America Whole-House Solutions for New Homes: William Ryan Homes, Tampa, Florida Buildng America Whole-House Solutions for New Homes: William Ryan Homes, Tampa, Florida Case ...

  3. EAC Recommendations for DOE Action Regarding Non-Wires Solutions...

    Office of Environmental Management (EM)

    Non-Wires Solutions - October 17, 2012 EAC Recommendations for DOE Action Regarding Non-Wires Solutions - October 17, 2012 EAC Recommendations for DOE Action Regarding Non-Wires...

  4. GreenSource Solutions LLC | Open Energy Information

    Open Energy Info (EERE)

    GreenSource Solutions LLC Jump to: navigation, search Name: GreenSource Solutions LLC Place: Novato, California Zip: 94945 Product: US-based PV system installer and consulting....

  5. Keeping Climate Change Solutions on Track: The Role of Rail ...

    Open Energy Info (EERE)

    Keeping Climate Change Solutions on Track: The Role of Rail Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Keeping Climate Change Solutions on Track: The Role of Rail...

  6. Enterprise Business Solutions EBS Group | Open Energy Information

    Open Energy Info (EERE)

    Business Solutions EBS Group Jump to: navigation, search Name: Enterprise Business Solutions (EBS Group) Product: US-based group with plans to set up 5MW PV project in the state of...

  7. Renewable Energy Solutions Inc RESI | Open Energy Information

    Open Energy Info (EERE)

    Solutions Inc RESI Jump to: navigation, search Name: Renewable Energy Solutions Inc (RESI) Place: Ewing, New Jersey Zip: 08638-2400 Product: US-based developer of PV manufacturing...

  8. Friction Control Solutions Inc FriCSo | Open Energy Information

    Open Energy Info (EERE)

    Friction Control Solutions Inc FriCSo Jump to: navigation, search Name: Friction Control Solutions Inc. (FriCSo) Place: Farmington Hills, Michigan Zip: 48331 Product: FriCSo offers...

  9. DOE Exercises 5 Year Option on Washington TRU Solutions Contract...

    Energy Savers [EERE]

    DOE Exercises 5 Year Option on Washington TRU Solutions Contract to Operate WIPP DOE Exercises 5 Year Option on Washington TRU Solutions Contract to Operate WIPP January 18, 2005 -...

  10. National Clean Energy Business Plan Competition: FGC Plasma Solutions...

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

    their method, FGC Plasma Solutions plans to integrate plasma-assisted combustion topology with a fuel nozzle-developed as a plug and play solution-which can be easily...

  11. Regional Climate Vulnerabilities and Resilience Solutions | Department of

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

    Energy Regional Climate Vulnerabilities and Resilience Solutions Regional Climate Vulnerabilities and Resilience Solutions This interactive map is not viewable in your browser. Please view it in a modern browser.

  12. DOE Zero Energy Ready Home: Building America Solution Center...

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

    Building America Solution Center, presented in April 2014. Lindsay Parker: We're really excited that you can join us today for the session on the Building America Solution Center....

  13. Text-Alternative Version: Evaluating LED Street Lighting Solutions

    Office of Energy Efficiency and Renewable Energy (EERE)

    Below is the text-alternative version of the Evaluating LED Street Lighting Solutions webcast, held July 20, 2010.

  14. Method for preparing salt solutions having desired properties

    DOE Patents [OSTI]

    Ally, Moonis R. (Oak Ridge, TN); Braunstein, Jerry (Clinton, TN)

    1994-01-01

    The specification discloses a method for preparing salt solutions which exhibit desired thermodynamic properties. The method enables prediction of the value of the thermodynamic properties for single and multiple salt solutions over a wide range of conditions from activity data and constants which are independent of concentration and temperature. A particular application of the invention is in the control of salt solutions in a process to provide a salt solution which exhibits the desired properties.

  15. Building America Technology Solutions for New and Existing Homes...

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

    Cambridge, Massachusetts Building America Technology Solutions for New and Existing Homes: Boiler Control Replacement for Hydronically Heated Multifamily Buildings, Cambridge, ...

  16. Workplace Charging Challenge Partner: Bosch Automotive Service Solutions,

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

    Inc. | Department of Energy Bosch Automotive Service Solutions, Inc. Workplace Charging Challenge Partner: Bosch Automotive Service Solutions, Inc. Workplace Charging Challenge Partner: Bosch Automotive Service Solutions, Inc. Bosch Automotive Service Solutions is committed to reducing their carbon footprint. As a part of that commitment, Bosch has implemented a workplace charging policy that makes plug-in electric vehicle (PEV) charging available to their associates. Providing the

  17. Sneak Peek into the Better Buildings Residential Program Solution Center

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

    Webinar | Department of Energy Sneak Peek into the Better Buildings Residential Program Solution Center Webinar Sneak Peek into the Better Buildings Residential Program Solution Center Webinar Sneak Peek into the Better Buildings Residential Program Solution Center Webinar, from the U.S. Department of Energy's Better Buildings Neighborhood Program. File Sneak Peek into the Better Buildings Residential Program Solution Center Webinar More Documents & Publications How to Work With the

  18. Method for liquid chromatographic extraction of strontium from acid solutions

    DOE Patents [OSTI]

    Horwitz, E. Philip (Naperville, IL); Dietz, Mark L. (Evanston, IL)

    1992-01-01

    A method and apparatus for extracting strontium and technetium values from biological, industrial and environmental sample solutions using a chromatographic column is described. An extractant medium for the column is prepared by generating a solution of a diluent containing a Crown ether and dispersing the solution on a resin substrate material. The sample solution is highly acidic and is introduced directed to the chromatographic column and strontium or technetium is eluted using deionized water.

  19. Discover the New Better Buildings Residential Program Solution Center |

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

    Department of Energy Discover the New Better Buildings Residential Program Solution Center Discover the New Better Buildings Residential Program Solution Center A transcript of "Discover the New Better Buildings Residential Program Solution Center," Better Buildings Neighborhood Program Webcast, June 19, 2014. PDF icon Solution Center webinar transcript More Documents & Publications Home Performance with ENERGY STAR Webinar (text version) Sustainable Energy Resources for

  20. Building America Technology Solutions for New and Existing Homes...

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

    Insulation Strategies, Minneapolis, Minnesota Building America Technology Solutions for New and Existing Homes: Innovative Retrofit Foundation Insulation Strategies, ...