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1

Extraction and recovery of plutonium and americium from nitric acid waste solutions by the TRUEX process - continuing development studies  

SciTech Connect (OSTI)

This report summarizes the work done to date on the application of the TRUEX solvent extraction process for removing and separately recovering plutonium and americium from a nitric acid waste solution containing these elements, uranium, and a complement of inert metal ions. This simulated waste stream is typical of a raffinate from a tributyl phosphate (TBP)-based solvent extraction process for removing uranium and plutonium from dissolved plutonium-containing metallurgical scrap. The TRUEX process solvent in these experiments was a solution of TBP and octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO) dissolved in carbon tetrachloride. A flowsheet was designed on the basis of measured batch distribution ratios to reduce the TRU content of the solidified raffinate to less than or equal to 10 nCi/g and was tested in a countercurrent experiment performed in a 14-stage Argonne-model centrifugal contractor. The process solvent was recycled without cleanup. An unexpectedly high evaporative loss of CCl/sub 4/ resulted in concentration of the active extractant, CMPO, to nearly 0.30M in the solvent. Results are consistent with this higher CMPO concentration. The raffinate contained only 2 nCi/g of TRU, but the higher CMPO concentration resulted in reduced effectiveness in the stripping of americium from the solvent. Conditions can be easily adjusted to give high yields and good separation of americium and plutonium. Experimental studies of the hydrolytic and gamma-radiolytic degradation of the TRUEX-CCl/sub 4/ showed that solvent degradation would be (1) minimal for a year of processing this typical feed, which contained no fission products, and (2) could be explained almost entirely by hydrolytic and radiolytic damage to TBP. Even for gross amounts of solvent damage, scrubbing with aqueous sodium carbonate solution restored the original americium extraction and stripping capability of the solvent. 43 refs., 5 figs., 36 tabs.

Leonard, R.A.; Vandegrift, G.F.; Kalina, D.G.; Fischer, D.F.; Bane, R.W.; Burris, L.; Horwitz, E.P.; Chiarisia, R.; Diamond, H.

1985-09-01T23:59:59.000Z

2

Method for removing fluoride contamination from nitric acid  

SciTech Connect (OSTI)

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

Howerton, W.B.; Pruett, D.J.

1982-07-13T23:59:59.000Z

3

Recovery of mercury from acid waste residues  

DOE Patents [OSTI]

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

Greenhalgh, W.O.

1987-02-27T23:59:59.000Z

4

Recovery of mercury from acid waste residues  

DOE Patents [OSTI]

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

Greenhalgh, Wilbur O. (Richland, WA)

1989-01-01T23:59:59.000Z

5

Removal of fluoride from aqueous nitric acid  

SciTech Connect (OSTI)

Several methods for removing fluoride from aqueous nitric acid were investigated and compared with the frequently used aluminum nitrate-calcium nitrate (Ca/sup 2 +/-Al/sup 3 +/) chemical trap-distillation system. Zirconium oxynitrate solutions were found to be superior in preventing volatilization of fluoride during distillation of the nitric acid, producing decontamination factors (DFs) on the order of 2 x 10/sup 3/ (vs approx. 500 for the Ca/sup 2 +/-Al/sup 3 +/ system). Several other metal nitrate systems were tested, but they were less effective. Alumina and zirconia columns proved highly effective in removing HF from HF-HNO/sub 3/ vapors distilled through the columns; fluoride DFs on the order of 10/sup 6/ and 10/sup 4/, respectively, were obtained. A silica gel column was very effective in adsorbing HF from HF-HNO/sub 3/ solutions, producing a fluoride DF of approx. 10/sup 4/.

Pruett, D.J.; Howerton, W.B.; Mailen, J.C.

1981-06-01T23:59:59.000Z

6

EFFECTS OF NITRIC ACID ON CRITICALITY SAFETY ANALYSIS  

SciTech Connect (OSTI)

As nitric acid molarity is increased, there are two competing phenomena affecting the reactivity of the system. First, there is interaction between each of the 10 wells in the basket-like insert. As the molarity of the nitric acid solution is increased (it moves from 100% water to 100% HNO{sub 3}), the hydrogen atom density decreases by about 80%. However, it remains a relatively efficient moderator. The moderating ratio of nitric acid is about 90% that of water. As the media between the wells is changed from 100% water to 100% nitric acid, the density of the media increases by 50%. A higher density typically leads to a better reflector. However, when the macroscopic scattering cross sections are considered, nitric acid is a much worse reflector than water. The effectiveness of nitric acid as a reflector is about 40% that of water. Since the media between the wells become a worse reflector and still remains an effective moderator, interaction between the wells increases. This phenomenon will cause reactivity to increase as nitric acid molarity increases. The seond phenomenon is due to the moderating ratio changing in the high concentration fissile-nitric acid solution in the 10 wells. Since the wells contain relatively small volumes of high concentration solutions, a small decrease in moderating power has a large effect on reactivity. This is due to the fact that neutrons are more likely to escape the high concentration fissile solution before causing another fission event. The result of this phenomenon is that as nitric acid molarity increases, reactivity decreases. Recent studies have shown that the second phenomenon is indeed the dominating force in determining reactivity changes in relation to nitric acid molarity changes. When considering the system as a whole, as nitric acid molarity increases, reactivity decreases.

Williamson, B.

2011-08-18T23:59:59.000Z

7

Extraction of nitric acid, uranyl nitrate, and bismuth nitrate from aqueous nitric acid solutions with CMPO  

SciTech Connect (OSTI)

DOE sponsored development of the transuranium extraction (TRUEX) process for removing actinides from radioactive wastes. The solvent is a mixture of CMPO and TBP. Since the extraction characteristics of CMPO are not as well understood as those of TBP, the extraction of nitric acid, uranyl nitrate, and bismuth nitrate with CMPO (dissolved in n-dodecane) were studied. Results indicate that CMPO extracts nitric acid with a 1:1 stoichiometry; equilibrium constant is 2. 660{plus_minus}0.092 at 25 C, and extraction enthalpy is -5. 46{plus_minus}0.46 kcal/mol. Slope analysis indicates that uranyl nitrate extracts with a mixed equilibria of 1:1 and 2:1 stoichiometries in nearly equal proportion. Equil. constant of the 2: 1 extraction was 1.213 {times} 10{sup 6}{plus_minus}3.56 {times} 10{sup 4} at 25 C; reaction enthalpy was -9.610{plus_minus}0.594 kcal/mol. Nitration complexation constant is 8.412{plus_minus}0.579, with an enthalpy of -10.72{plus_minus}1.87 kcal/mol. Bismuth nitrate also extracts with a mixed equilibria of (perhaps) 1:1 and 2:1 stoichiometries. A 2:1 extraction equilibrium and a nitrate complexation adequately model the data. Kinetics and enthalpies were also measured.

Spencer, B.B.

1995-08-01T23:59:59.000Z

8

Mercury-free dissolution of aluminum-clad fuel in nitric acid  

DOE Patents [OSTI]

A mercury-free dissolution process for aluminum involves placing the aluminum in a dissolver vessel in contact with nitric acid-fluoboric acid mixture at an elevated temperature. By maintaining a continuous flow of the acid mixture through the dissolver vessel, an effluent containing aluminum nitrate, nitric acid, fluoboric acid and other dissolved components are removed. 5 figs.

Christian, J.D.; Anderson, P.A.

1994-11-15T23:59:59.000Z

9

Mercury-free dissolution of aluminum-clad fuel in nitric acid  

DOE Patents [OSTI]

A mercury-free dissolution process for aluminum involves placing the aluminum in a dissolver vessel in contact with nitric acid-fluoboric acid mixture at an elevated temperature. By maintaining a continuous flow of the acid mixture through the dissolver vessel, an effluent containing aluminum nitrate, nitric acid, fluoboric acid and other dissolved components are removed.

Christian, Jerry D. (Idaho Falls, ID); Anderson, Philip A. (Pocatello, ID)

1994-01-01T23:59:59.000Z

10

Extraction of antimony from nitric acid solutions using tributyl phosphate. I. Tributyl phosphate-antimony(III)-nitric acid system  

SciTech Connect (OSTI)

Experimental data have been reported concerning the extraction of trivalent antimony from nitric acid solutions using tributyl phosphate (TBP). A possible mechanism for the extraction of antimony(III) has been determined and the (pre)concentration constant for the process has been calculated. The effect of temperature on trivalent antimony extraction has also been evaluated. The enthalpy value and standard isobar potential and entropy for this process have been determined.

Lakaev, V.S.; Smelov, V.S.

1989-01-01T23:59:59.000Z

11

Extraction of antimony from nitric acid solutions using tributyl phosphate. II. Tributyl phosphate-antimony(V)-nitric acid system  

SciTech Connect (OSTI)

The extraction of pentavalent antimony from nitric acid solutions using tributyl phosphate has been investigated. A possible mechanism for the extraction of antimony(V) has been determined and the (pre)concentration constant for the process has been calculated. The composition of the extracted antimony(V) complex has been deduced. A negative effect of temperature on the distribution coefficient for antimony(V) has also been demonstrated.

Lakaev, V.S.; Smelov, V.S.

1989-01-01T23:59:59.000Z

12

Process for the recovery of strontium from acid solutions  

DOE Patents [OSTI]

The invention is a process for selectively extracting strontium and technetium values from aqueous nitric acid waste solutions containing these and other fission product values. The extractant is a macrocyclic polyether in a diluent which is insoluble in water, but which will itself dissolve a small amount of water. The process will extract strontium and technetium values from nitric acid solutions which are up to 6 molar in nitric acid.

Horwitz, E. Philip (Naperville, IL); Dietz, Mark L. (Evanston, IL)

1992-01-01T23:59:59.000Z

13

Process for the recovery of strontium from acid solutions  

DOE Patents [OSTI]

The invention is a process for selectively extracting strontium and technetium values from aqueous nitric acid waste solutions containing these and other fission product values. The extractant is a macrocyclic polyether in a diluent which is insoluble in water, but which will itself dissolve a small amount of water. The process will extract strontium and technetium values from nitric acid solutions which are up to 6 molar in nitric acid. 5 figs.

Horwitz, E.P.; Dietz, M.L.

1992-03-31T23:59:59.000Z

14

Nitric-phosphoric acid oxidation of organic waste materials  

SciTech Connect (OSTI)

A wet chemical oxidation technology has been developed to address issues facing defense-related facilities, private industry, and small-volume generators such as university and medical laboratories. Initially tested to destroy and decontaminate a heterogenous mixture of radioactive-contaminated solid waste, the technology can also remediate other hazardous waste forms. The process, unique to Savannah River, offers a valuable alternative to incineration and other high-temperature or high-pressure oxidation processes. The process uses nitric acid in phosphoric acid; phosphoric acid allows nitric acid to be retained in solution well above its normal boiling point. The reaction converts organics to carbon dioxide and water, and generates NO{sub x} vapors which can be recycled using air and water. Oxidation is complete in one to three hours. In previous studies, many organic compounds were completely oxidized, within experimental error, at atmospheric pressure below 180{degrees}C; more stable compounds were decomposed at 200{degrees}C and 170 kPa. Recent studies have evaluated processing parameters and potential throughputs for three primary compounds: EDTA, polyethylene, and cellulose. The study of polyvinylchloride oxidation is incomplete at this time.

Pierce, R.A.; Smith, J.R.

1995-11-01T23:59:59.000Z

15

Chemistry of tributyl phosphate and nitric acid at constant volume  

SciTech Connect (OSTI)

This paper addresses the reaction of tributyl phosphate (TBP) with nitric acid (HNO{sub 3}). The reaction pressure of TBP/HNO{sub 3} mixtures as a function of time was measured under constant volume. A simplified model, which parametrically includes autocatalysis, was used to plot the total gas production of the reaction as a function of time. Comparison of the functions shows a rough equivalence in the induction time, reaction time, and total gas production. Predictions of the amounts of reaction products as a function of time were made based on assumptions regarding autocatalysis and using rate constants from experimental data. The derived reaction mechanisms and experimental results have several implications. Tests with a large amount of venting and high surface to volume ratio will show very different behavior than tests with increasing confinement and low surface to volume ratios. The amount alkyl nitrate, carbon monoxide, or hydrogen that reacts within the organic phase is limited by their solubilities and volatilities. The overall yield of both heat and gas per mol of nitric acid or TBP will vary significantly depending on the amount of solution, free volume, and vessel vent capacity.

Agnew, S.F.; Eisenhawer, S.W.; Morris, J.S. [Los Alamos National Lab., NM (United States)

1995-12-31T23:59:59.000Z

16

Analysis of Steam Heating of a Two-Layer TBP/N-Paraffin/Nitric Acid Mixtures  

SciTech Connect (OSTI)

This report presents an analysis of steam heating of a two-layer tri-n-butyl phosphate (TBP)/n-paraffin-nitric acid mixture.The purpose of this study is to determine if the degree of mixing provided by the steam jet or by bubbles generated by the TBP/nitric acid reaction is sufficient to prevent a runaway reaction.

Laurinat, J.E. [Westinghouse Savannah River Company, AIKEN, SC (United States); Hassan, N.M.; Rudisill, T.S.; Askew, N.M.

1998-07-22T23:59:59.000Z

17

Transportation impact analysis for the shipment of low specific activity nitric acid. Revisison 1  

SciTech Connect (OSTI)

This is in support of the Plutonium-Uranium Extraction (PUREX) Facility Low Specific Activity (LSA) Nitric Acid Shipment Environmental Assessment. It analyzes potential toxicological and radiological risks associated with transportation of PUREX Facility LSA Nitric Acid from the Hanford Site to Portsmouth VA, Baltimore MD, and Port Elizabeth NJ.

Green, J.R.

1995-05-16T23:59:59.000Z

18

Quantifying wet scavenging processes in aircraft observations of nitric acid and cloud condensation nuclei  

E-Print Network [OSTI]

Quantifying wet scavenging processes in aircraft observations of nitric acid and cloud condensation indicator for quantifying wet scavenging. Specifically, nitric acid (HNO3), produced as a by-product of combustion, is highly soluble and removed efficiently from clouds by rain. Regional carbon monoxide (CO

Palmer, Paul

19

Amino acid treatment enhances protein recovery from sediment...  

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

treatment enhances protein recovery from sediment and soils for metaproteomic studies . Amino acid treatment enhances protein recovery from sediment and soils for metaproteomic...

20

Effect of the TBP and Water on the Complexation of Uranyl Nitrate and the Dissolution of Nitric Acid into Supercritical CO2. A Theoretical Study  

E-Print Network [OSTI]

started from "random" mixtures of water, TBP, nitric acid, and uranyl nitrate, complexation of uranyl to dissolve nitric acid in the supercritical phase. Indeed, without TBP, nitric acid alone self aggregates via containing the acid and uranyl salts. The simulations show that a high TBP/nitric acid ratio is needed

Boyer, Edmond

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


21

Scandium nitrate-nitric acid-water-tributyl phosphate system. III. IR spectra of scandium extracts from concentrated nitric acid solutions  

SciTech Connect (OSTI)

Equilibrium organic phases in extraction systems consisting of tributyl phosphate (TBP) (neat or 1 M in CCl{sub 4}) and 8-12 M nitric acid containing scandium or scandium-free have been studied by IR spectroscopy. Extracted complex contains 3, 4, or 5 nitric acid molecules per Sc atom in the case of extraction from 8.3, 10.9, and 12.2 M HNO{sub 3}, respectively, and corresponds to the formula Sc(NO{sub 3}){sub 3}{center_dot}mHNO{sub 3}{center_dot}3TBP. Nitric acid molecules are incorporated into extracted complex via H-bond between oxygen atom of coordinated nitrate ion and acid proton.

Nikitina, G.P.; Egorova, V.P.; Listopadov, A.A. [Khlopin Radium Institute, St. Petersburg (Russian Federation)] [and others

1995-03-01T23:59:59.000Z

22

Features of gadolinium and ytterbium extraction by tributyl phosphate from concentrated nitric acid solutions. I. Compositions of extracted complexes  

SciTech Connect (OSTI)

Distribution of macroquantity (0.3-1.3 M) of Gd and Yb between neat tri-n-butyl phosphate (TBP) and 5-12 M nitric acid solutions has been studied. The species extracted by TBP from 7-12 M nitric acid solutions are rare-earth metal (REM) nitrate trisolvates containing one or several nitric molecules.

Nikitna, G.P.; Seredkina, N.V.; Listopadov, A.A. [Khlopin Radium Institute, St. Petersburg (Russian Federation)

1995-01-01T23:59:59.000Z

23

Amino acids, polyamines, and nitric oxide synthesis in the ovine conceptus  

E-Print Network [OSTI]

The objective of this study was to determine concentrations of amino acids and polyamines as well as nitric oxide (NO) and polyamine synthesis in the ovine conceptus (embryo/fetal and associated placental membrane). Ewes were hysterectomized...

Kwon, Hyuk Jung

2005-08-29T23:59:59.000Z

24

E-Print Network 3.0 - abandoned nitric acid Sample Search Results  

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

plants... In addition to the natural processes that form small amounts of nitric acid in rainwater, high-temperature air... combustion, such as occurs in car engines and power...

25

THE SYSTEM THORIUM NITRATE-WATER-NITRIC ACID AT 25 AND THE HYDRATES...  

Office of Scientific and Technical Information (OSTI)

SYSTEM THORIUM NITRATE-WATER-NITRIC ACID AT 25 AND THE HYDRATES OF THORIUM NITRATE Re-direct Destination: Temp Data Fields Ferraro, J.R.; Katzin, L.I. Temp Data Storage 3: Argonne...

26

THE SYSTEM THORIUM NITRATE-WATER-NITRIC ACID AT 25 AND THE HYDRATES...  

Office of Scientific and Technical Information (OSTI)

SYSTEM THORIUM NITRATE-WATER-NITRIC ACID AT 25 AND THE HYDRATES OF THORIUM NITRATE Re-direct Destination: times redirected to final destination ShortURL Code Published Current...

27

Isothermal heat measurements of TBP-nitric acid solutions  

SciTech Connect (OSTI)

Net heats of reaction were measured in an isothermal calorimeter for TBP/HNO{sub 3} solutions at ambient pressure and temperatures above 100{degrees}C. Carbon and nitrogen balances were performed giving the reaction stoichiometry. Rate expressions were derived and rate constants determined for both the single and two phase systems which included mass lost from the reacting system by evaporation. This mathematical model was fit to the experimental data (including the measured net heat and off-gas rate) gathered over a wide range of conditions. The oxidation rate constant was determined to be 5.4E-4 min{sup -1} at 110{degrees}C for an open {open_quotes}vented{close_quotes} system as compared to >1E-3min{sup -1} in a closed system. The heat released per unit material oxidized was also reduced due to a decrease in dissolved oxidants and an inefficient reduction of HNO{sub 3}. Oxidation in the organic phase was found to be first order in nitric acid and pseudo-zero order in butylnitrate and water.

Smith, J.R.; Cavin, W.S. [Westinghouse Savannah River Company, Aiken, SC (United States)

1995-12-31T23:59:59.000Z

28

Disposition and transportation of surplus radioactive low specific activity nitric acid. Volume 1, Environmental Assessment  

SciTech Connect (OSTI)

DOE is deactivating the PUREX plant at Hanford; this will involve the disposition of about 692,000 liters (183,000 gallons) of surplus nitric acid contaminated with low levels of U and other radionuclides. The nitric acid, designated as low specific activity, is stored in 4 storage tanks at PUREX. Five principal alternatives were evaluated: transfer for reuse (sale to BNF plc), no action, continued storage in Hanford upgraded or new facility, consolidation of DOE surplus acid, and processing the LSA nitric acid as waste. The transfer to BNF plc is the preferred alternative. From the analysis, it is concluded that the proposed disposition and transportation of the acid does not constitute a major federal action significantly affecting the quality of the human environment within the meaning of NEPA; therefore an environmental impact statement is not required.

NONE

1995-05-01T23:59:59.000Z

29

Laboratory studies of 2H evaporator scale dissolution in dilute nitric acid  

SciTech Connect (OSTI)

The rate of 2H evaporator scale solids dissolution in dilute nitric acid has been experimentally evaluated under laboratory conditions in the SRNL shielded cells. The 2H scale sample used for the dissolution study came from the bottom of the evaporator cone section and the wall section of the evaporator cone. The accumulation rate of aluminum and silicon, assumed to be the two principal elemental constituents of the 2H evaporator scale aluminosilicate mineral, were monitored in solution. Aluminum and silicon concentration changes, with heating time at a constant oven temperature of 90 deg C, were used to ascertain the extent of dissolution of the 2H evaporator scale mineral. The 2H evaporator scale solids, assumed to be composed of mostly aluminosilicate mineral, readily dissolves in 1.5 and 1.25 M dilute nitric acid solutions yielding principal elemental components of aluminum and silicon in solution. The 2H scale dissolution rate constant, based on aluminum accumulation in 1.5 and 1.25 M dilute nitric acid solution are, respectively, 9.21E-04 ± 6.39E-04 min{sup -1} and 1.07E-03 ± 7.51E-05 min{sup -1}. Silicon accumulation rate in solution does track the aluminum accumulation profile during the first few minutes of scale dissolution. It however diverges towards the end of the scale dissolution. This divergence therefore means the aluminum-to-silicon ratio in the first phase of the scale dissolution (non-steady state conditions) is different from the ratio towards the end of the scale dissolution. Possible causes of this change in silicon accumulation in solution as the scale dissolution progresses may include silicon precipitation from solution or the 2H evaporator scale is a heterogeneous mixture of aluminosilicate minerals with several impurities. The average half-life for the decomposition of the 2H evaporator scale mineral in 1.5 M nitric acid is 12.5 hours, while the half-life for the decomposition of the 2H evaporator scale in 1.25 M nitric acid is 10.8 hours. Based on averaging the two half-lives from the 2H scale acid dissolution in 1.25 and 1.5 M nitric acid solutions, a reasonable half-live for the dissolution of 2H scales in dilute nitric acid is 11.7 ± 1.3 hours. The plant operational time for chemically cleaning (soaking) the 2H evaporator with dilute nitric acid is 32 hours. It therefore may require about 3 half-lives or less to completely dissolve most of the scales in the Evaporator pot which come into contact with the dilute nitric acid solution. On a mass basis, the Al-to-Si ratio for the scale dissolution in 1.5 M nitric acid averaged 1.30 ± 0.20 and averaged 1.18 ± 0.10 for the 2H scale dissolution in 1.25 M nitric acid. These aluminum-to-silicon ratios are in fairly good agreement with ratios from previous studies. Therefore, there is still more aluminum in the 2H evaporator scales than silicon which implies that there are no significant changes in scale properties which will exclude nitric acid as a viable protic solvent for aluminosilicate scale buildup dissolution from the 2H evaporator. Overall, the monitoring of the scale decomposition reaction in 1.25 and 1.5 M nitric acid may be better ascertained through the determination of aluminum concentration in solution than monitoring silicon in solution. Silicon solution chemistry may lead to partial precipitating of silicon with time as the scale and acid solution is heated.

Oji, L.

2014-09-23T23:59:59.000Z

30

Isothermal heat measurements of TBP-nitric acid solutions  

SciTech Connect (OSTI)

Net heats of reaction were measured in an isothermal calorimeter for both single phase (organic) and two phase (organic and aqueous) TBP/HNO{sub 3} reacting solutions at temperatures above 100 C. The oxidation rate constant was determined to be 5.4E-4 min{sup {minus}1} at 110 C for an open ``vented`` system as compared to 1.33 E-3 min{sup {minus}1} in the closed system. The heat released per unit material oxidized was also reduced. The oxidation in both phases was found to be first order in nitric acid and pseudo-zero order in butylnitrate and water. The hydrolysis (esterification) rate constant determined by Nichols` (1.33E-3 min{sup {minus}1}) fit the experimental data from this work well. Forced evaporation of the volatile components by the product gases from oxidation resulted in a cooling mechanism which more than balanced the heat from the oxidation reaction in the two-phased systems. Rate expressions were derived and rate constants determined for both the single and two phase systems. An approximating mathematical model was developed to fit the experimental data and to extrapolate beyond the experimental conditions. This model shows that one foot of ``reacting`` 14.3M HNO{sub 3} aqueous phase solution at 121 C will transport sufficient water to the organic phase to replace evaporative losses, maintaining endothermicity, for organic layers up to 12.2 + 6.0 feet deep. If the pressure in a reacting system is allowed to increase due to insufficient venting the temperature of the organic phase would increase in temperature to reach a new equilibrium. The rate of oxidation would increase not only due to the increase in temperature but also from the increased concentration of dissolved HNO{sub 3} reduction products. Another important factor is that the cooling system described in this work becomes less effective as the total pressure increases. These factors probably contributed to the explosion at Tomsk.

Smith, J.R.; Cavin, W.S.

1994-12-16T23:59:59.000Z

31

Third phase formation in nitric acid extraction by n-octyl(phenyl)-n,n-diisobutylcarbamoylmethylphosphine oxide  

SciTech Connect (OSTI)

The third phase formation was studied as a function of n-octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO) and tri-n-butyl phosphate (TBP) concentrations and temperature in the extraction of nitric acid. The concentration fractions of CMPO and TBP in the second and the third phases were determined by gas chromatography. Both CMPO and TBP were found to be enriched in the third phase. The concentrations of nitric acid in the second and the third phases relatively agreed with the calculated concentrations based on the extraction equilibrium constants of nitric acid by CMPO and TBP. The extraction of Np with the third phase formation was also discussed. 21 refs., 4 figs., 3 tabs.

Nagasaki, S.; Wisnubroto, D.S.; Enokida, Y.; Suzuki, A. (Univ. of Tokyo (Japan))

1994-03-01T23:59:59.000Z

32

Reactivity of tributyl phosphate degradation products with nitric acid: Relevance to the Tomsk-7 accident  

SciTech Connect (OSTI)

The reaction of a degraded tributyl phosphate (TBP) solvent with nitric acid is thought to have caused the chemical explosion at the Tomsk-7 reprocessing plant at Tomsk, Russia in 1993. The estimated temperature of the organic layer was not high eneough to cause significant reaction of nitric acid with TBP or hydrocarbon diluent compounds. A more reactive organic compound was likely present in the organic layer that reacted with sufficient heat generation to raise the temperature to the point where an autocatalytic oxidation of the organic solvent was initiated. Two of the most likely reactive compounds that are present in degraded TBP solvents are n-butanol and n-butyl nitrate. The reactions of these compounds with nitric acid are the subject of this study. The objective of laboratory-scale tests was to identify chemical reactions that occur when n-butanol and n-butyl nitrate contact heated nitric acid solutions. Reaction products were identified and quantitified, the temperatures at which these reactions occur and heats of reaction were measured, and reaction variables (temperature, nitric acid concentration, organic concentration, and reaction time) were evaluated. Data showed that n-butyl nitrate is less reactive than n-butanol. An essentially complete oxidation reaction of n-butanol at 110-120 C produced four major reaction products. Mass spectrometry identified the major inorganic oxidation products for both n-butanol and n-butyl nitrate as nitric oxide and carbon dioxide. Calculated heats of reaction for n-butanol and n-butyl nitrate to form propionic acid, a major reaction product, are -1860 cal/g n-butanol and -953 cal/g n-butyl nitrate. These heats of reaction are significant and could have raised the temperature of the organic layer in the Tomsk-7 tank to the point where autocatalytic oxidation of other organic compounds present resulted in an explosion.

Barney, G.S.; Cooper, T.D. [Westinghouse Hanford Company, Richland, WA (United States)

1995-12-31T23:59:59.000Z

33

Evaporative Hydrochloric Acid Recovery: Something Old, Something New...  

E-Print Network [OSTI]

. If zinc is present from the pickling of galvanizing racks or stripping of parts, the zinc concentration will range from as low as zinc chloride solution remains. In the evaporative process of the Hydrochloric Acid Recovery System, the waste acid is pumped through a pre-filter into the evaporator section oftI1e recovery system. This solution is heated by means...

Cullivan, B.

34

CHARACTERIZATION OF H CANYON CONDUCTIVITY METER INDICATIONS WITH ELEVATED URANIUM IN NITRIC ACID  

SciTech Connect (OSTI)

Solution conductivity data from the 1CU conductivity meter in H-Canyon shows that uranium concentration in the 0 to 30 gram per liter (g/L) range has no statistically significant effect on the calibration of free nitric acid measurement. Based on these results, no additional actions are needed on the 1CU Conductivity Meter prior to or during the processing of uranium solutions in the 0 to 30 g/L range. A model based only on free nitric acid concentration is shown to be appropriate for explaining the data. Data uncertainties for the free acid measurement of uranium-bearing solutions are 8.5% or less at 95% confidence. The analytical uncertainty for calibrating solutions is an order of magnitude smaller only when uranium is not present, allowing use of a more accurate analytical procedure. Literature work shows that at a free nitric acid level of 0.33 M, uranium concentration of 30 g/L and 25 C, solution conductivity is 96.4% of that of a uranium-free solution. The level of uncertainties in the literature data and its fitting equation do not justify calibration changes based on this small depression in solution conductivity. This work supports preparation of H-Canyon processing of Super Kukla fuel; however, the results will be applicable to the processing of any similar concentration uranium and nitric acid solution. Super Kukla fuel processing will increase the uranium concentration above the nominal zero to 10 g/L level, though not above 30 g/L. This work examined free nitric acid levels ranging from 0.18 to 0.52 molar. Temperature ranged from 27.9 to 28.3 C during conductivity testing. The data indicates that sequential order of measurement is not a significant factor. The conductivity meter was thus flushed effectively between measurements as desired.

Nash, C

2007-10-31T23:59:59.000Z

35

Control of nitric acid plant stack opacity during start-up and shutdown  

SciTech Connect (OSTI)

This patent describes an improvement in a process for the production of nitric acid wherein air and ammonia are mixed and combusted in an ammonia burner to produce an effluent containing nitrogen oxides. The effluent is cooled, condensed and separated into a liquid weak acid stream and gas stream. The liquid weak acid and vapor streams are fed into an absorber tower wherein they are countercurrently contacted with water to produce a nitric acid stream and an overhead with a reduced nitrogen oxides content. The overhead is combusted with a fuel in the presence of a catalyst in a catalytic combustor to produce a combustor exhaust, work expanded in an expander to recover energy and vented to the atmosphere as stack exhaust. The improvement involves controlling the opacity of the stack opacity during shutdown of the process.

Adams, J.B.; Gasper, J.A.; Stash, P.J.

1989-09-26T23:59:59.000Z

36

Oleic AcidDependent Modulation of NITRIC OXIDE ASSOCIATED1 Protein Levels Regulates Nitric  

E-Print Network [OSTI]

of Agriculture­Agricultural Research Service, Washington State University, Prosser, Washington 99350 acid, which induces anti-inflammatory effects (Denys et al., 2001). FAs also serve as alarm molecules also regulate salt, drought, and heavy metal tolerance as well as wounding-induced responses

Kachroo, Pradeep

37

Mediated electrochemical oxidation of organic wastes using a Co (III) mediator in a nitric acid based system  

DOE Patents [OSTI]

An electrochemical cell with a Co(III) mediator and nitric acid electrolyte provides efficient destruction of organic and mixed wastes. The organic waste is concentrated in the anolyte reservoir, where the mediator oxidizes the organics and insoluble transuranic compounds and is regenerated at the anode until the organics are converted to CO[sub 2]. The nitric acid is an excellent oxidant that facilitates the destruction of the organic components. The anode is not readily attacked by the nitric acid solution, thus the cell can be used for extended continual operation without electrode replacement. 2 figs.

Balazs, G.B.; Chiba, Z.; Lewis, P.R.; Nelson, N.; Steward, G.A.

1999-06-15T23:59:59.000Z

38

Mediated electrochemical oxidation of organic wastes using a Co (III) mediator in a nitric acid based system  

DOE Patents [OSTI]

An electrochemical cell with a Co(III) mediator and nitric acid electrolyte provides efficient destruction of organic and mixed wastes. The organic waste is concentrated in the anolyte reservoir, where the mediator oxidizes the organics and insoluble transuranic compounds and is regenerated at the anode until the organics are converted to CO.sub.2. The nitric acid is an excellent oxidant that facilitates the destruction of the organic components. The anode is not readily attacked by the nitric acid solution, thus the cell can be used for extended continual operation without electrode replacement.

Balazs, G. Bryan (Livermore, CA); Chiba, Zoher (Moraga, CA); Lewis, Patricia R. (Livermore, CA); Nelson, Norvell (Palo Alto, CA); Steward, G. Anthony (Los Altos Hills, CA)

1999-01-01T23:59:59.000Z

39

A thermodynamic model of nitric acid extraction by tri-n-butyl phosphate  

SciTech Connect (OSTI)

A thermodynamic model is presented for nitric acid extraction by tri-n-butyl phosphate (TBP). This model is based on the formation of the organic phase species: TBP.HNO/sub 3/ and (TBP)/sub 2/.HNO/sub 3/. The model works successfully at TBP concentrations of 5 to 100 vol% and was found to be effective at predicting the extraction of HNO/sub 3/ from HNO/sub 3//NaNO/sub 3/ and HNO/sub 3//LiNO/sub 3/ solutions. Within the TBP concentration range of 5 to 30%, a single set of extraction constants was sufficient to fit extraction data. Stoichiometric activity coefficients of nitric acid in HNO/sub 3//NaNO/sub 3/ and HNO/sub 3//LiNO/sub 3/ mixtures were calculated using a model developed by Bromley.

Chaiko, D.J.; Vandegrift, G.F.

1988-07-01T23:59:59.000Z

40

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

SciTech Connect (OSTI)

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.

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

2000-09-28T23:59:59.000Z

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


41

Scandium nitrate-nitric acid-water-tributyl phosphate system. I. Scandium extraction isotherms  

SciTech Connect (OSTI)

A study has been made of scandium distribution between neat tributyl phosphate (TBP) and 0.2-1.2 M scandium solutions in 2.7-12.3 M nitric acid. Scandium extracts in equilibrium with 0.2-1 M Sc in 6-12 M HNO{sub 3} contain from 2 to 5 HNO{sub 3} molecules per scandium atom in extracted Sc complex.

Listopadov, A.A.; Nikitina, G.P.; Egorova, V.P. [Khlopin Radium Institute, St. Petersburg (Russian Federation)] [and others

1995-01-01T23:59:59.000Z

42

Influence of uranium on corrosion of stainless steel in solutions of fluoride in nitric acid  

SciTech Connect (OSTI)

Stainless steels corrode rapidly in solutions of fluoride in nitric acid; the higher the fluoride ion content, the more intense is the corrosion. The activating effect of the fluoride ions mainly reduces to dissolution of the oxide films. Small amounts somewhat retard the cathodic reduction of HNO/sub 3/. In this report the authors provide the results of an investigation of the influence of uranium ions on the corrosion-electrochemical behavior of stainless steel 12Kh18N10T in solutions of up to 10 moles/liter of HNO/sub 3/, with fluoride ions up to 0.1 mole/liter. The authors conclude that the retardation of corrosion of stainless steel by uranium, zirconium and aluminum ions in solutions of fluorides in nitric acid is mainly due to the formation of strong complexes of these metals with fluorine ions, leading to a reduction of the number of free HF molecules in the solution. The stronger the complex of metal with fluorine, the higher the corrosion resistance of the stainless steel in a solution of fluoride in nitric acid.

Kurtenov, M.M.

1985-09-01T23:59:59.000Z

43

Initiation Temperature for Runaway Tri-n-Butyl Phosphate/Nitric Acid Reaction  

SciTech Connect (OSTI)

During a review of the H-Canyon authorization basis, Defense Nuclear Facility Safety Board (DNFSB) staff members questioned the margin of safety associated with a postulated tri-n-butyl phosphate (TBP)/nitric acid runaway reaction due to the inadvertent heating of a canyon tank containing greater than 3000 lbs (1362 kg) of TBP. The margin of safety was partially based on experiments and calculations performed by the Actinide Technology Section (ATS) to support deletion of indication of tank agitation as a Safety Class System. In the technical basis for deletion of this system, ATS personnel conservatively calculated the equilibrium temperature distribution of a canyon tank containing TBP and nitric acid layers which were inadvertently heated by a steam jet left on following a transfer. The maximum calculated temperature (128 degrees C) was compared to the minimum initiation temperature for a runaway reaction (greater than 130 degrees C) documented by experimental work in the mid 195 0s. In this work, the initiation temperature as a function of nitric acid concentration was measured for 0 and 20 wt percent dissolved solids. The DNFSB staff members were concerned that data for 0 wt percent dissolved solids were not conservative given the facts that data for 20 wt percent dissolved solids show initiation temperatures at or below 130 degrees C and H-Canyon solutions normally contained a small amount of dissolved solids.

Rudisill, T.S.

2000-11-28T23:59:59.000Z

44

How Nitric Acid Overcame Its Fear of Water | EMSL  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsingFun withconfinement plasmas inPortalAllBPA addresses EMF BNitric Acid

45

FY13 GLYCOLIC-NITRIC ACID FLOWSHEET DEMONSTRATIONS OF THE DWPF CHEMICAL PROCESS CELL WITH SIMULANTS  

SciTech Connect (OSTI)

Savannah River Remediation is evaluating changes to its current Defense Waste Processing Facility flowsheet to replace formic acid with glycolic acid in order to improve processing cycle times and decrease by approximately 100x the production of hydrogen, a potentially flammable gas. Higher throughput is needed in the Chemical Processing Cell since the installation of the bubblers into the melter has increased melt rate. Due to the significant maintenance required for the safety significant gas chromatographs and the potential for production of flammable quantities of hydrogen, eliminating the use of formic acid is highly desirable. Previous testing at the Savannah River National Laboratory has shown that replacing formic acid with glycolic acid allows the reduction and removal of mercury without significant catalytic hydrogen generation. Five back-to-back Sludge Receipt and Adjustment Tank (SRAT) cycles and four back-to-back Slurry Mix Evaporator (SME) cycles were successful in demonstrating the viability of the nitric/glycolic acid flowsheet. The testing was completed in FY13 to determine the impact of process heels (approximately 25% of the material is left behind after transfers). In addition, back-to-back experiments might identify longer-term processing problems. The testing was designed to be prototypic by including sludge simulant, Actinide Removal Product simulant, nitric acid, glycolic acid, and Strip Effluent simulant containing Next Generation Solvent in the SRAT processing and SRAT product simulant, decontamination frit slurry, and process frit slurry in the SME processing. A heel was produced in the first cycle and each subsequent cycle utilized the remaining heel from the previous cycle. Lower SRAT purges were utilized due to the low hydrogen generation. Design basis addition rates and boilup rates were used so the processing time was shorter than current processing rates.

Lambert, D.; Zamecnik, J.; Best, D.

2014-03-13T23:59:59.000Z

46

Sorption of uranium from nitric acid solution using TBP-impregnated activated carbons  

SciTech Connect (OSTI)

The concept of extraction chromatography has been used to study the sorption of uranium from nitric acid solutions using tri-n-butyl phosphate (TBP) impregnated activated carbons. Batch equilibrium data and kinetic and breakthrough column behavior of uranium are reported. Wood based activated carbon has shown better capacity and breakthrough characteristics than shell based activated carbon. Sorption rate on impregnated carbons was relatively slow indicating that diffusion is the rate controlling step within the pore structure of the activated carbon. Uranium distribution on impregnated activated carbons is compared with equivalent bulk liquid extraction and a mechanism of uranium sorption is discussed.

Abbasi, W.A. [Pakistan Atomic Energy Commission, Islamabad (Pakistan). Pakistan Inst. of Nuclear Science and Technology; Streat, M. [Loughborough Univ. (United Kingdom). Dept. of Chemical Engineering

1998-08-01T23:59:59.000Z

47

Acid/Base Recovery From Sodium Sulfate  

E-Print Network [OSTI]

escalating In price due to the Imbalance In market demand. Chlorine and caustic are produced together by the electrolysis 01 sodium chloride brine solutions. Every ECU (electrochemical unit) 01 chlorine resu~s In the production 01 one ECU 01 caustic soda... cell also produces an acid product that is contaminated with unreacted sullate. The voltage 01 a three compartment is higher, however, and the process system Is more complex. Process System Current density and efficiency determines the amount 01...

Niksa, M. J.

48

Effect of temperature on the extraction of nitric acid and plutonium(IV) nitrate with 30 vol% tributyl phosphate (TBP)  

SciTech Connect (OSTI)

The author's own and published data were evaluated for characterizing the effect of temperature on the distribution of nitric acid and plutonium(IV). The solutes were distributed between 30 vol% TBP in an aliphatic diluent and aqueous solutions containing nitric acid and zero to macro amounts of plutonium(IV) and uranyl nitrates. The temperature dependence of the distribution ratios is described with empirical model equations and examples of the dependence in the absence and presence of uranium(VI) are given. Taking infinite dilution of all solutes of the system as a standard state, the enthalpy change of the extraction reaction could be estimated as -17 kJ/mol for nitric acid, but no numerical estimate was possible for plutonium(IV).

Kolarik, Z.

1984-01-01T23:59:59.000Z

49

Features of gadolinium and ytterbium extraction by tributyl phosphate from concentrated nitric acid solutions. II. IR spectra of lanthanide extracts  

SciTech Connect (OSTI)

Equilibrium organic phases in extraction systems consisting of tributyl phosphate (TBP) (neat or 1.8 M in CCl{sub 4}) and 8-12 M nitric acid containing Gd or Yb or lanthanide-free have been studied by IR spectroscopy. It was shown that under these conditions lanthanides are extracted as complex trisolvates Ln(NO{sub 3})9{sub 3}{center_dot}mHNO{sub 3}{center_dot}3TBP with m = 3-6. Nitric acid molecules are H-bonded to oxygen atoms of coordinated nitrate ions and do not substitute TBP molecules in coordination sphere of the metal ion.

Nikitina, G.P.; Seredkina, N.V.; Kistopadov, A.A. [Khlopin Radium Institute, St. Petersburg (Russian Federation)

1995-03-01T23:59:59.000Z

50

Separation of uranium from nitric and hydrochloric acid solutions with extractant-coated magnetic microparticles.  

SciTech Connect (OSTI)

The magnetically assisted chemical separation (MACS) process utilizes selective magnetic microparticle composites to separate dissolved metals from solution. In this study, MACS particles were coated with neutral and acidic organophosphorus extractants,octyl(phenyl)-N,N-diisobutylcarbamoylmethyl phosphine oxide (CMPO), tributyl phosphate (TBP), trioctylphosphine oxide (TOPO), and bis(2-ethyl-hexyl)phosphoric acid (D{sub 2}EHPA or HDEHP) and were evaluated for the separation of uranyl ions from nitric- and hydrochloric-acid solutions. The results suggest that a synergistic interaction between the particle surface and solvent coating may explain why the particles display, in some cases, orders of magnitude of higher partitioning coefficients than are estimated from solvent-extraction measurements. Particles coated with TBP and those coated with a combination of TOPO and D{sub 2}EHPA displayed the most desirable characteristics for removing uranium from dilute acid environments typical of contaminated groundwater. Uranium separation from moderate to highly acidic waste streams typical of Department of Energy (DOE) nuclear wastes is best accomplished using particles coated with a combination of CMPO and TBP.

Kaminski, M. D.; Nunez, L.; Chemical Engineering

2000-01-01T23:59:59.000Z

51

Safe conditions for contacting nitric acid or nitrates with tri-n-butyl phosphate (TBP)  

SciTech Connect (OSTI)

In response to a request from DOE-SR, the current state of knowledge of the reactions between TBP and aqueous nitrate solutions is critically reviewed, and recommendations are made for the safe operation of SRS separations equipment in which this combination of chemicals may be present. The existing limits for evaporation are validated. Guidelines are presented for cases in which general limits do not apply. The rate of reaction between nitric acid and TBP appears to be controlled by the rate of TBP hydrolysis. The hydrolysis reaction produces dibutyl phosphate and n-butanol. The hydrolysis rate is a strong function of temperature, and becomes very fast at temperatures in the range 130{degrees} to 150{degrees}C. The resulting n-butanol is volatile at high temperatures, boiling at 117.5{degrees}C, but is also subject to exothermic oxidation by nitric acid or nitrates. If oxidation occurs before the n-butanol evaporates, the heat of oxidation may exceed local cooling by convection. The resulting heating will further accelerate the reaction, leading to an energetic runaway and possibly (in confined systems) an explosion. Extensive experiments and practice have shown that in a well-mixed and well-vented aqueous system such as an evaporator, at moderate acidities and temperatures below 130{degrees}C, the heat of reaction is adequately removed by vaporization of steam. In general, the heating will be so slow that natural processes provide adequate cooling at temperatures below 80{degrees}C. Above this temperature, care should be taken to ensure that adequate cooling is available for the amount of TBP that may be present. Experiments suggest that in well-ventilated systems n-butanol evaporation and convective cooling are sufficient to control the reaction at temperatures up to 120{degrees}C.

Hyder, M.L

1994-01-01T23:59:59.000Z

52

Nitric Acid Deposition following an Astrophysical Ionizing Radiation Event is below Critical Loads for Terrestrial and Freshwater Ecosystems  

E-Print Network [OSTI]

Nitric acid rainout is one of the effects of an astrophysical ionizing radiation event. The predicted values of nitrate rainout from previous work for a typical gamma ray burst (GRB) within our galaxy serve as an extreme example and are shown to be below critical loads of eutrophication and acidification for ecoregions in Europe and the US.

Melott, Ben Neuenswander Adrian

2014-01-01T23:59:59.000Z

53

Corrosion property of 9Cr-ODS steel in nitric acid solution for spent nuclear fuel reprocessing  

SciTech Connect (OSTI)

Corrosion tests of oxide dispersion strengthened with 9% Cr (9Cr-ODS) steel, which is one of the desirable materials for cladding tube of sodium-cooled fast reactors, in pure nitric acid solution, spent FBR fuel solution, and its simulated solution were performed to understand the corrosion behavior in a spent nuclear fuel reprocessing. In this study, the 9Cr-ODS steel with lower effective chromium content was evaluated to understand the corrosion behavior conservatively. As results, the tube-type specimens of the 9Cr-ODS steels suffered severe weight loss owing to active dissolution at the beginning of the immersion test in pure nitric acid solution in the range from 1 to 3.5 M. In contrast, the weight loss was decreased and they showed a stable corrosion in the higher nitric acid concentration, the dissolved FBR fuel solution, and its simulated solution by passivation. The corrosion rates of the 9Cr-ODS steel in the dissolved FBR fuel solution and its simulated solution were 1-2 mm/y and showed good agreement with each other. The passivation was caused by the shift of corrosion potential to noble side owing to increase in nitric acid concentration or oxidative ions in the dissolved FBR fuel solution and the simulated spent fuel solution. (authors)

Takeuchi, M.; Koizumi, T. [Japan Atomic Energy Agency, Tokai-mura, Naka-gun, Ibaraki 319-1195 (Japan); Inoue, M.; Koyama, S.I. [Japan Atomic Energy Agency, Oarai-machi, Higashi-ibaraki-gun, Ibaraki 311-1393 (Japan)

2013-07-01T23:59:59.000Z

54

Initiation Temperature for Runaway Tri-n-Butyl Phosphate/Nitric Acid Reaction  

SciTech Connect (OSTI)

In a review of the safety basis for solvent extraction processes at the Department of Energy's Savannah River Site, a question was raised concerning the safety margin associated with a postulated accident involving a runaway tri-n-butyl phosphate (TBP)/nitric acid reaction due to the inadvertent heating of a tank. The safety margin was based on studies which showed the maximum temperature would not exceed 128 degrees Celsius compared to 130 degrees Celsius, the minimum initiation temperature for runaway reaction established in the 1950's following damaging incidents at the Savannah River and Hanford Sites. The reviewers were concerned the minimum temperature was not conservative since data for solutions containing 20 wt percent dissolved solids showed initiation temperatures at or below 130 degrees Celsius and process solutions normally contain some dissolved solids.

Rudisill, T.S.

2001-09-14T23:59:59.000Z

55

Novel Regenerated Solvent Extraction Processes for the Recovery of Carboxylic Acids or Ammonia from Aqueous Solutions Part I. Regeneration of Amine-Carboxylic Acid Extracts  

E-Print Network [OSTI]

production of citric acid by fermentation, recovery of theof Citric Acid from Aqueous Fermentation Solutions byof citric acid was 1.1.1 Lactic Acid Currently, fermentation

Poole, L.J.

2008-01-01T23:59:59.000Z

56

Extraction equilibria between organic CMPO-n-dodecane and aqueous nitric acid phases for selected tank waste components  

SciTech Connect (OSTI)

Removal of the transuranium elements from tank-stored wastes is an important step in the cost effective treatment and preparation of these wastes for permanent disposal. One promising method of treatment involves dissolving the tank sludges in acid, followed by extraction of the transuranium species. The TRUEX process, which uses an extracting medium composed of octyl(phenyl)-N,N-diisobutylcarbamoylmethyl phosphine oxide (CMPO) and tri-n-butyl phosphate (TBP) dissolved in an organic solvent such as n-dodecane, is being tested for this purpose. Although CMPO is a powerful extractant for all the actinides, concern arises that certain process chemicals present in the waste will compete for the CMPO. Data will be presented on the pure component equilibrium characteristics of nitric acid, uranyl nitrate and bismuth nitrate partitioned between a nitric acid aqueous phase and a CMPO-n-dodecane organic phase.

Spencer, B.B.; Egan, B.Z. [Oak Ridge National Lab., TN (United States); Counce, R.M. [Univ. of Tennessee, Knoxville, TN (United States)

1996-10-01T23:59:59.000Z

57

MATERIAL COMPATIBILITY EVALUATION FOR DWPF NITRIC-GLYCOLIC ACID - LITERATURE REVIEW  

SciTech Connect (OSTI)

Glycolic acid is being evaluated as an alternative for formic and nitric acid in the DWPF flowsheet. Demonstration testing and modeling for this new flowsheet has shown that glycolic acid and glycolate has a potential to remain in certain streams generated during the production of the nuclear waste glass. A literature review was conducted to assess the impact of glycolic acid on the corrosion of the materials of construction for the DWPF facility as well as facilities downstream which may have residual glycolic acid and glycolates present. The literature data was limited to solutions containing principally glycolic acid. The reported corrosion rates and degradation characteristics have shown the following for the materials of construction. ? For C276 alloy, the primary material of construction for the CPC vessels, corrosion rates of either 2 or 20 mpy were reported up to a temperature of 93 ?C. ? For the austenitic stainless steels, 304L and 316L, variable rates were reported over a range of temperatures, varying from 2 mpy up to 200 mpy (at 100 ?C). ? For 690, G30, Allcorr, Ultimet and Stellite alloys no data were available. ? For relevant polymers where data are available, the data suggests that exposure to glycolic acid is not detrimental. The literature data had limited application to the DWPF process since only the storage and feed vessels, pumps and piping used to handle the glycolic acid are directly covered by the available data. These components are either 304L or 316L alloys for which the literature data is inconsistent (See Bullet 2 above). Corrosion rates in pure glycolic acid solutions also are not representative of the DWPF process streams. This stream is complex and contains aggressive species, i.e. chlorides, sulfates, mercury, as well as antifoaming agents which cumulatively have an unknown effect on the corrosion rates of the materials of construction. Therefore, testing is recommended to investigate any synergistic effects of the aggressive species and to verify the performance of materials in the key process vessels as well as downstream vessels and processes such as the evaporator where heating is occurring. The following testing would provide data for establishing the viability of these components. ? Electrochemical testing - evaluate the corrosion rate and susceptibility to localized corrosion within the SRAT, SME, OGCT, Quencher and Evaporator. Testing would be conducted at operational temperatures in simulants with ranges of glycolic acid, iron, chloride, sulfate, mercury, and antifoaming agents. ? Hot-wall testing – evaluate the corrosion under heat transfer conditions to simulate those for heating coils and evaporator coil surfaces. Testing would be at nominal chemistries with concentration of glycolic acid, chloride, sulfate and mercury at high expected concentrations. Some tests would be performed with antifoaming agents. ? Melter coupon testing – evaluate the performance of alloy 690 in melter feeds containing glycolic acid. This testing would be conducted as part of the melter flammability testing. ? Polymer testing – evaluate changes in polymer properties in immersion testing with DWPF simulants to provide product-specific data for service life evaluation and analyze the Hansen solubility parameters for relevant polymers in glycolic vs. formic acid. During this literature review process, the difficulties associated with measuring the liquid level in formic acid tanks were revealed. A test is recommended to resolve this issue prior to the introduction of glycolic acid into the DWPF. This testing would evaluate the feasibility of using ultrasonic inspection techniques to determine liquid level and other desirable attributes of glycolic acid in DWPF storage tanks and related equipment.

Mickalonis, J.; Skidmore, E.

2013-06-05T23:59:59.000Z

58

Thermal acidization and recovery process for recovering viscous petroleum  

DOE Patents [OSTI]

A thermal acidization and recovery process for increasing production of heavy viscous petroleum crude oil and synthetic fuels from subterranean hydrocarbon formations containing clay particles creating adverse permeability effects is described. The method comprises injecting a thermal vapor stream through a well bore penetrating such formations to clean the formation face of hydrocarbonaceous materials which restrict the flow of fluids into the petroleum-bearing formation. Vaporized hydrogen chloride is then injected simultaneously to react with calcium and magnesium salts in the formation surrounding the bore hole to form water soluble chloride salts. Vaporized hydrogen fluoride is then injected simultaneously with its thermal vapor to dissolve water-sensitive clay particles thus increasing permeability. Thereafter, the thermal vapors are injected until the formation is sufficiently heated to permit increased recovery rates of the petroleum.

Poston, Robert S. (Winter Park, FL)

1984-01-01T23:59:59.000Z

59

Amides as phase modifiers for N,N{prime}-tetraalkylmalonamide extraction of actinides and lanthanides from nitric acid solutions  

SciTech Connect (OSTI)

The N,N{prime}-tetraalkylmalonamides are a class of compounds under development for transuranic (TRU) separations under high nitric acid conditions. There are several issues that challenge the further development of these ligands. One is the development of improved synthetic procedures that lend themselves to commercial scale-up. Another major issue is the third-phase formation that occurs when the N,N{prime}-tetraalkylmalonamides are contacted with medium-to-high nitric acid concentrations in hydrocarbon solvents. To address the synthesis issue, the authors have developed a new synthetic approach for preparing these materials. Third-phase formation can be eliminated by addition of diluent modifiers such as tributylphosphate (TBP). TBP is inappropriate if a nonphosphate-containing process stream is required. Amides have been proposed as alternatives for TBP in a variety of applications because of their ease of synthesis and the variety of substituents that can be generated. The authors have been able to develop an amide phase-modified system that extends the working process range of alkylinalonamides (0.5 M) in dodecane: from 3.5 M to 7.5 M nitric acid and in Isopar H (branched hydrocarbon) from 4.0 M to 10.0 M nitric acid using 1.0 M di-2-ethylhexylacetamide/0.5 M alkylmalonamide. The Kd values were comparable to extraction with alkylinalonamide in Isopar H or hydrogenated tetrapropylene (TPH) solvents. The overall extraction system was more robust than the phase-uninodified system allowing for greater temperature and acid concentration fluctuations without third-phase formation.

Smith, B.F.; Wilson, K.V.; Gibson, R.R. [Los Alamos National Lab., NM (United States)

1997-01-01T23:59:59.000Z

60

Heterogeneous Chemistry of Individual Mineral Dust Particles with Nitric Acid. A Combined CCSEM/EDX, ESEM AND ICP-MS Study  

SciTech Connect (OSTI)

The heterogeneous chemistry of individual dust particles from four authentic dust samples with gas-phase nitric acid was investigated in this study. Morphology and compositional changes of individual particles as they react with nitric acid were observed using conventional scanning electron microscopy with energy dispersive analysis of X-rays (SEM/EDX) and computer controlled SEM/EDX. Environmental Scanning Electron Microscopy (ESEM) was utilized to investigate the hygroscopic behavior of mineral dust particles reacted with nitric acid. Differences in the reactivity of mineral dust particles from these four different dust source regions with nitric acid were observed. Mineral dust from source regions containing high levels of calcium, namely China loess dust and Saudi coastal dust, were found to react to the greatest extent.

Laskin, Alexander; Wietsma, Thomas W.; Krueger, Brenda J.; Grassian, Vicki H.

2005-05-26T23:59:59.000Z

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


61

Remedial investigation report on the abandoned nitric acid pipeline at the Oak Ridge Y-12 Plant, Oak Ridge, Tennessee  

SciTech Connect (OSTI)

Upper East Fork Poplar Creek OU-2 consists of the Abandoned Nitric Acid Pipeline. This pipeline was installed in 1951 to transport liquid wastes {approximately} 4,800 ft from Buildings 9212, 9215, and 9206 to the S-3 Ponds. Materials known to have been discharged through the pipeline include nitric acid, depleted and enriched uranium, various metal nitrates, salts, and lead skimmings. A total of nineteen locations were chosen to be investigated along the pipeline for the first phase of this Remedial Investigation. Sampling consisted of drilling down to obtain a soil sample at a depth immediately below the pipeline. Additional samples were obtained deeper in the subsurface depending upon the depth of the pipeline, the depth of the water table, and the point of auger refusal. The nineteen samples collected below the pipeline were analyzed by the Y-12 Plant laboratory for metals, nitrate/nitrite, and isotopic uranium. Samples collected from three boreholes were also analyzed for volatile organic compounds because these samples produced a response with organic vapor monitoring equipment. The results of the baseline human health risk assessment for the Abandoned Nitric Acid Pipeline contaminants of potential concern show no unacceptable risks to human health via incidental ingestion of soil, inhalation of dust, dermal contact with the soil, or external exposure to radionuclides in the ANAP soils, under the construction worker and/or the residential land-use scenarios.

Not Available

1993-12-01T23:59:59.000Z

62

The effect of fluoride and aluminum on the anion exchange of plutonium from nitric acid  

SciTech Connect (OSTI)

Anion exchange in nitric acid is a prominent aqueous process used to recover and purify plutonium from impure nuclear materials. This process is sensitive to fluoride ion, which complexes plutonium in competition with the anionic nitrato complex that is strongly sorbed on the anion exchange column. Fluoride interference traditionally has been counteracted by adding a masking agent, such as aluminum, that forms competing complexes with fluoride. The interfering effect of fluoride is known to be a function not only of the fluoride-to-aluminum ratio but also of the fluoride-to-plutonium ratio. This report summarizes a Los Alamos study of the effect of 25 fluoride-aluminum-plutonium conmbinations on the anion exchange sorption of plutonium. Five aluminum-to-plutonium ratios ranging from 0.10 to 10 were each evaluated at five fluoride-to-aluminum ratios that ranged from 0 to 6. The fluoride-to-plutonium ratio has a greater influence on plutonium sorption than does the fluoride-to-aluminum ratio. Aluminum was less effective as a masking agent than had been assumed, because measurable fluoride interference occurred at all levels of added aluminum.

Marsh, S.F.

1987-07-01T23:59:59.000Z

63

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

DOE Patents [OSTI]

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

Michaels, E.D.

1981-02-25T23:59:59.000Z

64

Dissolution of plutonium oxide in nitric acid at high hydrofluoric acid concentrations  

SciTech Connect (OSTI)

The dissolution of plutonium dioxide in nitirc acid (HNO/sub 3/) at high hydrofluoric acid (HF) concentrations has been investigated. Dissolution rate curves were obtained using 12M HNO/sub 3/ and HF at concentrations varying from 0.05 to 1.0 molar. The dissolution rate increased with HF concentration up to 0.2M and then decreased at higher concentrations. There was very little plutonium dissolved at 0.7 and 1.0M HF because of the formation of insoluble PuF/sub 4/. Various oxidizing agents were added to 12M HNO/sub 3/-1M HF dissolvent to oxidize Pu(IV) to Pu(VI) and prevent the formation of PuF/sub 4/. Ceric (Ce(IV)) and silver (Ag(II)) ions were the most effective in dissolving PuO/sub 2/. Although these two oxidants greatly increased the dissolution rate, the rates were not as rapid as those obtained with 12M HNO/sub 3/-0.2M HF.

Kazanjian, A.R.; Stevens, J.R.

1984-06-15T23:59:59.000Z

65

Mercury extraction by the TRUEX process solvent: I. Kinetics, extractable species, dependence on nitric acid concentration and stoichiometry  

SciTech Connect (OSTI)

Mercury extraction from acidic aqueous solutions by the TRUEX process solvent (0.2 M CMPO, 1.4 M TBP in n-dodecane) has not extensively been examined. Research at the Idaho Chemical Processing Plant is currently in progress to evaluate the TRUEX process for actinide removal from several acidic waste streams, including liquid sodium-bearing waste (SBW), which contains significant quantities of mercury. Preliminary experiments were performed involving the extraction of Hg{sup 203}, added as HgCl{sub 2}, from 0.01 to 10 M HNO{sub 3} solutions. Mercury distribution coefficients (D{sub Hg}) range between 3 and 60 from 0.01 M to 2 M HNO{sub 3}. At higher nitric acid concentrations, i.e. 5 M HNO{sub 3} or greater, D{sub Hg} significantly decreases to values less than 1. These results indicate mercury is extracted from acidic solutions {<=}{approximately}2 M HNO{sub 3} and stripped with nitric acid solutions {>=}{approximately}5 M HNO{sub 3}. Experimental results indicate the extractable species is HgCl{sub 2} from nitrate media, i.e., chloride must be present in the nitrate feed to extract mercury. Extractions from Hg(NO{sub 3}){sub 2} solutions indicated substantially reduced distribution ratios, typically D{sub Hg}< 1, for the range of nitric acid concentrations examined (0.01 to 8 M HNO{sub 3}). Extraction of mercury, as HgCl{sub 2}, by the individual components of the TRUEX solvent was also examined from 2 M HNO{sub 3}. The diluent, n-dodecane, does not measurably extract mercury. With a 1.4 M TBP/n-dodecane solvent, D{sub Hg} {approximately}3.4 compared with D{sub Hg} {approximately}7 for the TRUEX solvent. Classical slope analysis techniques were utilized to evaluate the stoichiometric coefficients of Hg extraction independently for both CMPO and TBP.

Herbst, R.S.; Brewer, K.N.; Tranter, T.J.; Todd, T.A.

1995-12-01T23:59:59.000Z

66

RECOVERY OF LACTIC ACID FROM AMERICAN CRYSTAL SUGAR COMPANY WASTEWATER  

SciTech Connect (OSTI)

This project has shown that the recovery of several valuable lactic acid products is both technically feasible and economically viable. One of the original objectives of this project was to recover lactic acid. However, the presence of a variety of indigenous bacteria in the wastewater stream and technical issues related to recovery and purification have resulted in the production of lactic acid esters. These esters could by hydrolyzed to lactic acid, but only with unacceptable product losses that would be economically prohibitive. The developed process is projected to produce approximately 200,000 lb per day of lactate esters from wastewater at a single factory at costs that compete with conventional solvents. The lactate esters are good solvents for polymers and resins and could replace acetone, methyl ethyl ketone, MIBK, and other polar solvents used in the polymer industry. Because of their low volatility and viscosity-lowering properties, they will be especially useful for inks for jet printers, alkyl resins, and high-solid paints. Owing to their efficiency in dissolving salts and flux as well as oils and sealants, lactate esters can be used in cleaning circuit boards and machine and engine parts. Unlike conventional solvents, lactate esters exhibit low toxicity, are biodegradable, and are not hazardous air pollutants. Another application for lactate esters is in the production of plasticizers. Severe health problems have been attributed to widely used phthalate ester plasticizers. The U.S. Department of Agriculture showed that replacement of these with inexpensive lactate esters is feasible, owing to their superior polymer compatibility properties. A very large market is projected for polymers prepared from lactic acid. These are called polylactides and are a type of polyester. Thermoplastics of this type have a variety of uses, including moldings, fibers, films, and packaging of both manufactured goods and food products. Polylactides form tough, orientable, self-supporting thin films and have, therefore, been used for adhesives, safety glass, and finishes. If the bacterial culture produces the L-lactic acid enanatiomer form exclusively, the L-lactide prepared from this form can be used for making polymers with good fiber-forming properties. We have not currently achieved the exclusive production of L-lactate in our efforts. However, markets in films and structural shapes are available for polymers and copolymers prepared from the mixed D,L-lactide forms that result from processing the D,L-lactic acid obtained from fermentation such as that occurring naturally in sugar beet wastewater. These materials are slowly biodegraded to harmless compounds in the environment, and they burn with a clean blue flame when incinerated. These materials represent excellent opportunities for utilization of the D,L-lactic mixture produced from natural fermentation of the ACS flume water. Esters can be converted into a lactide, and the alcohol released from the ester can be recycled with no net consumption of the alcohol. Lactide intermediates could be produced locally and shipped to polymer producers elsewhere. The polymer and copolymer markets are extremely large, and the role of lactides in these markets is continuously expanding. The overall process can be readily integrated into existing factory wastewater operations. There are several environmental benefits that would be realized at the factories with incorporation of the lactate recovery process. The process reduces the organic loading to the existing wastewater treatment system that should result in enhanced operability with respect to both solids handling and treated-water quality. A higher-quality treated water will also help reduce odor levels from holding ponds. Several water reuse opportunities are probable, depending on the quality of treated water from the FT process.

Daniel J. Stepan; Edwin S. Olson; Richard E. Shockey; Bradley G. Stevens; John R. Gallagher

2001-04-30T23:59:59.000Z

67

Effect of temperature on the extraction of uranium(VI) from nitric acid by tri-n-amyl phosphate  

SciTech Connect (OSTI)

Studies have been carried out on the effect of temperature on the extraction of U(VI) from nitric acid medium by tri-n-amyl phosphate/n-dodecane, measured as a function of the extractant concentration and aqueous phase acidity. The results indicate that the extraction is exothermic as in the case of tri-n-butyl phosphate. From the data available an effort has been made to calculate the equilibrium constant, the Gibbs energy change and the entropy changes of the extraction reaction. 21 refs., 3 figs., 4 tabs.

Srinivasan, T.G.; Rao, P.R.V. [Indira Gandhi Centre for Atomic Research, Kalpakkam (India); Sood, D.D. [Indira Gandhi Centre for Atomic Research, Kalpakkam (India)]|[BARC, Mumbai (India)

1997-01-01T23:59:59.000Z

68

Nitric oxide donors prevent while the nitric oxide synthase inhibitor L-NAME increases arachidonic acid plus CYP2E1-dependent toxicity  

SciTech Connect (OSTI)

Polyunsaturated fatty acids such as arachidonic acid (AA) play an important role in alcohol-induced liver injury. AA promotes toxicity in rat hepatocytes with high levels of cytochrome P4502E1 and in HepG2 E47 cells which express CYP2E1. Nitric oxide (NO) participates in the regulation of various cell activities as well as in cytotoxic events. NO may act as a protectant against cytotoxic stress or may enhance cytotoxicity when produced at elevated concentrations. The goal of the current study was to evaluate the effect of endogenously or exogenously produced NO on AA toxicity in liver cells with high expression of CYP2E1 and assess possible mechanisms for its actions. Pyrazole-induced rat hepatocytes or HepG2 cells expressing CYP2E1 were treated with AA in the presence or absence of an inhibitor of nitric oxide synthase L-N {sup G}-Nitroarginine Methylester (L-NAME) or the NO donors S-nitroso-N-acetylpenicillamine (SNAP), and (Z)-1-[-(2-aminoethyl)-N-(2-aminoethyl)]diazen-1-ium-1,2-diolate (DETA-NONO). AA decreased cell viability from 100% to 48 {+-} 6% after treatment for 48 h. In the presence of L-NAME, viability was further lowered to 23 {+-} 5%, while, SNAP or DETA-NONO increased viability to 66 {+-} 8 or 71 {+-} 6%. The L-NAME potentiated toxicity was primarily necrotic in nature. L-NAME did not affect CYP2E1 activity or CYP2E1 content. SNAP significantly lowered CYP2E1 activity but not protein. AA treatment increased lipid peroxidation and lowered GSH levels. L-NAME potentiated while SNAP prevented these changes. Thus, L-NAME increased, while NO donors decreased AA-induced oxidative stress. Antioxidants prevented the L-NAME potentiation of AA toxicity. Damage to mitochondria by AA was shown by a decline in the mitochondrial membrane potential (MMP). L-NAME potentiated this decline in MMP in association with its increase in AA-induced oxidative stress and toxicity. NO donors decreased this decline in MMP in association with their decrease in AA-induced oxidative stress and toxicity. These results indicate that NO can be hepatoprotective against CYP2E1-dependent toxicity, preventing AA-induced oxidative stress.

Wu Defeng [Department of Pharmacology and Biological Chemistry, Box 1603, One Gustave L. Levy Place, Mount Sinai School of Medicine, New York, NY 10029 (United States); Cederbaum, Arthur [Department of Pharmacology and Biological Chemistry, Box 1603, One Gustave L. Levy Place, Mount Sinai School of Medicine, New York, NY 10029 (United States)]. E-mail: arthur.cederbaum@mssm.edu

2006-10-15T23:59:59.000Z

69

Solvent Extraction Behavior of Neptunium (IV) Ions between Nitric Acid and Diluted 30% Tri-butyl Phosphate in the Presence of Simple Hydroxamic Acids  

SciTech Connect (OSTI)

Formo- and aceto-hydroxamic acids are very effective reagents for stripping tetravalent actinide ions such as Np(IV) and Pu(IV) ions from a tri-butyl phosphate phase into nitric acid. Distribution data for Np(IV) in the presence of these hydroxamate ions have now been accumulated and trends established. Stability constants for aceto-hydroxamate complexes of Np(IV) and Np(V) ions have also been determined in a perchlorate medium, and these reaffirm the affinity of hydroxamate ligands for actinide (IV) ions over actinyl (V,VI) ions.

Taylor, Robin J.; Sinkov, Sergey I.; Choppin, Gregory R.; May, Iain

2008-01-15T23:59:59.000Z

70

Scandium nitrate-nitric acid-water-tributyl phosphate system. II. Interaction of Sc(NO{sub 3}){sub 3}{center_dot}3TBP with nitric acid in organic solvent  

SciTech Connect (OSTI)

Scandium nitrate solvates Sc(NO{sub 3}){sub 3}{center_dot}qTBP (TBP is tributyl phosphate, q = 3.15, 2.57, and 1.58) were synthesized, and their IR spectra were measured. Model solutions of Sc(NO{sub 3}){sub 3}{center_dot}3TBP in CCl{sub 4} containing nitric acid with Sc:HNO{sub 3} molar ratios 1:1 to 1:3 and 1:7 were prepared, and their IR spectra were also measured. The spectra indicate formation of complexes with formula Sc(NO{sub 3}){sub 3}{center_dot}mHNO{sub 3}{center_dot}3TBP (m = 1-7) through H-bonding of medium strength. In complexes with m = 1-2, nitric acid molecules are presumably bonded to oxygen atoms of nitrate groups coordinated to scandium. The R{sub O{hor_ellipsis}O} distance in these complexes was estimated for the H-bond as 2.68 {angstrom}.

Nikitina, G.P.; Papkov, K.B.; Listopadov, A.A. [Khlopin Radium Institute, St. Petersburg (Russian Federation)

1995-03-01T23:59:59.000Z

71

Synergistic selective extraction of actinides(III) over lanthanides from nitric acid using new aromatic diorganyldithiophosphinic acids and neutral organophosphorus compounds  

SciTech Connect (OSTI)

New aromatic dithiophosphinic acids (R{sub 2}PSSH) with R = C{sub 6}H{sub 5{sup {minus}}}, ClC{sub 6}H{sub 4{sup {minus}}}, FC{sub 6}H{sub 4{sup {minus}}} and CH{sub 3}C{sub 6}H{sub 4{sup {minus}}} were synthesized, characterized and tested as potential separating agents for trivalent actinides over lanthanides. The extraction of Am(III), Eu(III) and other lanthanides was carried out from nitric acid medium with mixtures of R{sub 2}PSSHs and neutral organophosphorus compounds. There was no detectable extraction when R{sub 2}PSSHs were used alone as extractants for either Am(III) or Eu(III) (D{sub Am,Eu} < 10{sup {minus}3}) under the experimental conditions used in this study. High separation factors (D{sub Am}/D{sub Eu} > 20) with D{sub Am} > 1 were achieved in the nitric acid range 0.1--1 mol/L by means of a synergistic mixture of bis(chlorophenyl)dithiophosphinic acid + tributylphosphate (TBP), trioctylphosphine oxide (TOPO) or tributylphosphine oxide (TBPO). The high radiation resistance (up to 10{sup 6} Gy absorbed {gamma}-doses) of the extractants was also demonstrated.

Modolo, G.; Odoj, R. [Forschungszentrum Juelich GmbH (Germany). Inst. fuer Sicherheitsforschung und Reaktortechnik

1999-01-01T23:59:59.000Z

72

Comparative evaluation of DHDECMP (dihexyl-N,N-diethylcarbamoyl-methylphosphonate) and CMPO (octylphenyl-N,N,-diisobutylcarbamoylmethylphosphine oxide) as extractants for recovering actinides from nitric acid waste streams  

SciTech Connect (OSTI)

Certain neutral, bifunctional organophosphorous compounds are of special value to the nuclear industry. Dihexyl-N,N-diethylcarbomoylmethylphosphonate (DHDECMP) and octylphenyl-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO) are highly selective extractants for removing actinide and lanthanide elements from nitric acid. We obtained these two extractants from newly available commercial sources and evaluated them for recovering Am(III), Pu(IV), and U(VI) from nitric acid waste streams of plutonium processing operations. Variables included the extractant (DHSECMP or CMPO), extractant/tributylphosphate ratio, diluent, nitrate concentration, nitrate salt/nitric acid ratio, fluoride concentration, and contact time. Based on these experimental data, we selected DHDECMP as the perferred extractant for this application. 18 refs., 30 figs.

Marsh, S.F.; Yarbro, S.L.

1988-02-01T23:59:59.000Z

73

GLYCOLIC-NITRIC ACID FLOWSHEET DEMONSTRATION OF THE DWPF CHEMICAL PROCESSING CELL WITH MATRIX SIMULANTS AND SUPERNATE  

SciTech Connect (OSTI)

Savannah River Remediation (SRR) is evaluating changes to its current DWPF flowsheet to improve processing cycle times. This will enable the facility to support higher canister production while maximizing waste loading. Higher throughput is needed in the CPC since the installation of the bubblers into the melter has increased melt rate. Due to the significant maintenance required for the DWPF gas chromatographs (GC) and the potential for production of flammable quantities of hydrogen, reducing or eliminating the amount of formic acid used in the CPC is being developed. Earlier work at Savannah River National Laboratory has shown that replacing formic acid with an 80:20 molar blend of glycolic and formic acids has the potential to remove mercury in the SRAT without any significant catalytic hydrogen generation. This report summarizes the research completed to determine the feasibility of processing without formic acid. In earlier development of the glycolic-formic acid flowsheet, one run (GF8) was completed without formic acid. It is of particular interest that mercury was successfully removed in GF8, no formic acid at 125% stoichiometry. Glycolic acid did not show the ability to reduce mercury to elemental mercury in initial screening studies, which is why previous testing focused on using the formic/glycolic blend. The objective of the testing detailed in this document is to determine the viability of the nitric-glycolic acid flowsheet in processing sludge over a wide compositional range as requested by DWPF. This work was performed under the guidance of Task Technical and Quality Assurance Plan (TT and QAP). The details regarding the simulant preparation and analysis have been documented previously.

Lambert, D.; Stone, M.; Newell, J.; Best, D.

2012-05-07T23:59:59.000Z

74

GLYCOLIC-NITRIC ACID FLOWSHEET DEMONSTRATION OF THE DWPF CHEMICAL PROCESS CELL WITH SLUDGE AND SUPERNATE SIMULANTS  

SciTech Connect (OSTI)

Savannah River Remediation (SRR) is evaluating changes to its current Defense Waste Processing Facility (DWPF) flowsheet to improve processing cycle times. This will enable the facility to support higher canister production while maximizing waste loading. Higher throughput is needed in the Chemical Process Cell (CPC) since the installation of the bubblers into the melter has increased melt rate. Due to the significant maintenance required for the DWPF gas chromatographs (GC) and the potential for production of flammable quantities of hydrogen, reducing or eliminating the amount of formic acid used in the CPC is being developed. Earlier work at Savannah River National Laboratory has shown that replacing formic acid with an 80:20 molar blend of glycolic and formic acids has the potential to remove mercury in the SRAT without any significant catalytic hydrogen generation. This report summarizes the research completed to determine the feasibility of processing without formic acid. In earlier development of the glycolic-formic acid flowsheet, one run (GF8) was completed without formic acid. It is of particular interest that mercury was successfully removed in GF8, no formic acid at 125% stoichiometry. Glycolic acid did not show the ability to reduce mercury to elemental mercury in initial screening studies, which is why previous testing focused on using the formic/glycolic blend. The objective of the testing detailed in this document is to determine the viability of the nitric-glycolic acid flowsheet in processing sludge over a wide compositional range as requested by DWPF. This work was performed under the guidance of Task Technical and Quality Assurance Plan (TT&QAP). The details regarding the simulant preparation and analysis have been documented previously.

Lambert, D.; Stone, M.; Newell, J.; Best, D.; Zamecnik, J.

2012-08-28T23:59:59.000Z

75

Corrosion of 304 Stainless Steel Exposed To Nitric Acid -Chloride Environments D.G. Kolman, D.K. Ford, D.P. Butt, and T.O. Nelson  

E-Print Network [OSTI]

Corrosion of 304 Stainless Steel Exposed To Nitric Acid - Chloride Environments D.G. Kolman, D.K. Ford, D.P. Butt, and T.O. Nelson Materials Corrosion and Environmental Effects Laboratory Los AlamosCl, and temperature on the general corrosion behavior of 304 stainless steel (SS), electrochemical studies were

76

Safety of Tri-n-butyl phosphate (TBP) and nitric acid solutions in two-phase systems at elevated temperatures  

SciTech Connect (OSTI)

This paper addresses the prevention of self-accelerating oxidation of nitric acid and tributyl phosphate (TBP). An accident of this type, which occurred at Tomsk-7, Russia, in 1993, resulted from a slow chemical reaction occurring initially at sub-boiling temperatures. The accumulating heat and vapors overpressurized and burst a process tank. Two safety issues are addressed in this summary of experimental data: circumstances under which convection or radiation cooling of vessels will exceed reaction heat, and measures which can prevent or mitigate such reactions. Heat generations rates have been found to range widely. Thermodynamic calculations confirm that heat generation is reduced by a large factor when nitrogen oxides are able to escape from the reaction mixure. Scoping calculations show that the evaporation of water is potentially the most effective mechanism for heat removal in a large vessel, and experiments have demonstrated that water evaporation is effective for preventing runaway reactions in a vented, two-phase system operated below about 120 C. These data indicate that venting is the key to controlling runaway reactions. However, other experiments have indicated that the self-heating reaction did not present a danger, even if reaction heating led to an accelerating reaction, in a sufficiently vented system. To determine how much venting was required, experiments were performed with pure organic phase and two-phase TBP-nitric acid mixtures. Data show a critical ratio of organic mass to vent area, above which the reacting system can reach potentially dangerous pressures. Experiments show runaway reactions occurring in vented systems only as the temperature approaches 130 C. These results clearly indicate that adequate venting of vessels containing heated TBP and nitrate is the key to controlling their reaction.

Hyder, M.L.; Paddleford, D.F.; Thompson, M.C. [Westinghouse Savannah River Company, Aiken, SC (United States)

1995-12-31T23:59:59.000Z

77

Studies on reaction runaways for Urex/Purex solvent-nitric acid and red-oil synthesis  

SciTech Connect (OSTI)

In PUREX/UREX processes for recycling of spent nuclear fuels, 30% TBP solvent is used, This solvent has a small solubility in the aqueous phase. During concentration of the process solutions by an evaporation route, a runaway reaction between TBP and nitric acid is initiated at above 130 deg. C, leading to rapid pressurization and finally containment failure if proper venting is not provided. Red oil was synthesized for the first time in India, and its physical properties as well as thermodynamic parameters for the reaction were determined. It was experimentally established that the presence of metallic nitrates was not essential for red-oil formation as thought earlier. Various experiments have been completed for single-phase as well as two-phase runs. The most important finding of this work was lowering of the limiting acid concentration from the conventional values. In fact, in these experiments, red oil could be formed even at 2 N aqueous acidity. Thus, safety guidelines based on the classical literature are obsolete. New guidelines for the red-oil-safety are required. (authors)

Kumar, Shekhar; Kumar, Rajnish; Koganti, S.B. [Reprocessing R and D Division, Reprocessing Group, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102 (India)

2008-07-01T23:59:59.000Z

78

THERMODYNAMICS OF EXTRACTION OF NITRIC ACID BY TRI-n-BUTYL PHOSPHATE--HYDROCARBON DILUENT SOLUTIONS  

E-Print Network [OSTI]

the mean act ivi ty coefficient T of TBP and TBP.H20 i n the acid-free, water-saturated organic phase

Wallace Davis

1961-01-01T23:59:59.000Z

79

Fermentation and recovery process for lactic acid production  

DOE Patents [OSTI]

A method is described for converting starch to glucose and fermenting glucose to lactic acid, including simultaneous saccharification and fermentation through use of a novel consortium of bacterial strains. 2 figs.

Tsai, S.P.; Moon, S.H.; Coleman, R.

1995-11-07T23:59:59.000Z

80

Preparation and recovery of methacrylic acid and its esters  

SciTech Connect (OSTI)

This patent describes a process for the vapor phase catalytic oxydehydrogenation of isobutyric acid or its esters to form methacrylic acid or its esters wherein the gaseous product is condensed and purified. The improvement described here consists of adding to the gaseous product at or about the point of its condensation from 1 to 6000 ppm of a surfactant material selected from the group consisting of an anionic a cationic and non-ionic surfactant.

Frank, P.J.; Hite, J.R.

1986-07-15T23:59:59.000Z

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


81

K Basin Sludge Conditioning Testing Nitric Acid Dissolution Testing of K East Area Sludge Composite, Small- and Large-Scale Testing  

SciTech Connect (OSTI)

This report describes work performed by Pacific Northwest National Laboratory (PNNL) for Numatec Hanford Corporation (NHC) to support the development of the K Basin Sludge Treatment System. For this work, testing was performed to examine the dissolution behavior of a K East Basin floor and Weasel Pit sludge composite, referred to as K East area sludge composite, in nitric acid at the following concentrations: 2 M, 4 M, 6 M and 7.8 M. With the exception of one high solids loading test the nitric acid was added at 4X the stoichiometric requirement (assuming 100% of the sludge was uranium metal). The dissolution tests were conducted at boiling temperatures for 24 hours. Most of the tests were conducted with {approximately}2.5 g of sludge (dry basis). The high solids loading test was conducted with {approximately}7 g of sludge. A large-scale dissolution test was conducted with 26.5 g of sludge and 620 mL of 6 M nitric acid. The objectives of this test were to (1) generate a sufficient quantity of acid-insoluble residual solids for use in leaching studies, and (2) examine the dissolution behavior of the sludge composite at a larger scale.

Carlson, C.D.; Delegard, C.H.; Burgeson, I.E.; Schmidt, A.J.; Silvers, K.L.

1999-04-02T23:59:59.000Z

82

PHOSPHORIC ACID EXTRACTION AND RARE EARTH RECOVERY FROM APATITES OF THE BRAZILIAN PHOSPHATIC ORES  

E-Print Network [OSTI]

so as to precipitate the rare earth elements as a phosphate concentrate. The application, fertilizer industry, rare earth elements recovery, phosphate rock, hydrochloric acid route. 1. Introduction: impossibility to recover high commercial value by-products such as the rare earth elements, existence of severe

Paris-Sud XI, Université de

83

Novel Regenerated Solvent Extraction Processes for the Recovery of Carboxylic Acids or Ammonia from Aqueous Solutions Part II. Recovery of Ammonia from Sour Waters  

SciTech Connect (OSTI)

Two novel regenerated solvent extraction processes are examined. The first process has the potential to reduce the energy costs inherent in the recovery of low-volatility carboxylic acids from dilute aqueous solutions. The second process has the potential for reducing the energy costs required for separate recovery of ammonia and acid gases (e.g. CO{sub 2} and H{sub 2}S) from industrial sour waters. The recovery of carboxylic acids from dilute aqueous solution can be achieved by extraction with tertiary amines. An approach for regeneration and product recovery from such extracts is to back-extract the carboxylic acid with a water-soluble, volatile tertiary amine, such as trimethylamine. The resulting trimethylammonium carboxylate solution can be concentrated and thermally decomposed, yielding the product acid and the volatile amine for recycle. Experimental work was performed with lactic acid, SUCCiOlC acid, and fumaric acid. Equilibrium data show near-stoichiometric recovery of the carboxylic acids from an organic solution of Alamine 336 into aqueous solutions of trimethylamine. For fumaric and succinic acids, partial evaporation of the aqueous back extract decomposes the carboxylate and yields the acid product in crystalline form. The decomposition of aqueous solutions of trimethylammonium lactates was not carried out to completion, due to the high water solubility of lactic acid and the tendency of the acid to self-associate. The separate recovery of ammonia and acid gases from sour waters can be achieved by combining steam-stripping of the acid gases with simultaneous removal of ammonia by extraction with a liquid cation exchanger. The use of di-2,4,4-trimethylpentyl phosphinic acid as the liquid cation exchanger is explored in this work. Batch extraction experiments were carried out to measure the equilibrium distribution ratio of ammonia between an aqueous buffer solution and an organic solution of the phosphinic acid (0.2N) in Norpar 12. The concentration-based distribution ratios increase from 0.11 to 0.46 as the aqueous phase pH increases from 7.18 to 8.15. Regeneration of the organic extractant solution was carried out by stripping at elevated temperatures to remove the ammonia, with 99% recovery of the ammonia being obtained at 125 C.

Poole, L.J.; King, C.J.

1990-03-01T23:59:59.000Z

84

A Pulse Radiolysis Investigation of the Reactions of Tributyl Phosphate with the Radical Products of Aqueous Nitric Acid Irradiation  

SciTech Connect (OSTI)

Tributyl phosphate (TBP) is the most common organic compound used in liquid-liquid separations for the recovery of uranium, neptunium, and plutonium from acidic nuclear fuel dissolutions. The goal of these processes is to extract the actinides while leaving fission products in the acidic, aqueous, phase. However, the radiolytic degradation of TBP has been shown to reduce the separation factors for fission products, and to impede the back-extraction of the actinides during stripping. As most previous investigations of the radiation chemistry of TBP have focused on steady state radiolysis and stable product identification, with dibutylphosphoric acid (HDBP) invariably being the major product, here we have determined room temperature rate constants for the reactions TBP and HDBP with the hydroxyl radical ((5.00 +/- 0.02) x 109, (4.40 +/- 0.10) x 109), hydrogen atom ((1.8 +/- 0.2) x 108, (1.1 +/- 0.1) x 108), nitrate radical ((4.3 +/- 0.7) x 106, (2.9 +/- 0.2) x 106) and nitrite radical (< 2 x 105, < 2 x 105) M-1 s-1 with TBP and HDBP, respectively. These data are used to discuss the mechanism of TBP radical-induced degradation.

Bruce J. Mincher; Stephen R. Mezyk; Leigh R. Martin

2008-07-01T23:59:59.000Z

85

Fourier Transform Infrared Spectroscopy and Multivariate Analysis for Online Monitoring of Dibutyl Phosphate Degradation Product in Tributyl Phosphate/n-Dodecane/Nitric Acid Solvent  

SciTech Connect (OSTI)

In liquid–liquid extraction separation processes, accumulation of organic solvent degradation products is detrimental to the process robustness, and frequent solvent analysis is warranted. Our research explores the feasibility of online monitoring of the organic solvents relevant to used nuclear fuel reprocessing. This paper describes the first phase of developing a system for monitoring the tributyl phosphate (TBP)/n-dodecane solvent commonly used to separate used nuclear fuel. In this investigation, the effect of extraction of nitric acid from aqueous solutions of variable concentrations on the quantification of TBP and its major degradation product dibutylphosphoric acid (HDBP) was assessed. Fourier transform infrared (FTIR) spectroscopy was used to discriminate between HDBP and TBP in the nitric acid-containing TBP/n-dodecane solvent. Multivariate analysis of the spectral data facilitated the development of regression models for HDBP and TBP quantification in real time, enabling online implementation of the monitoring system. The predictive regression models were validated using TBP/n-dodecane solvent samples subjected to high-dose external ?-irradiation. The predictive models were translated to flow conditions using a hollow fiber FTIR probe installed in a centrifugal contactor extraction apparatus, demonstrating the applicability of the FTIR technique coupled with multivariate analysis for the online monitoring of the organic solvent degradation products.

Tatiana G. Levitskaia; James M. Peterson; Emily L. Campbell; Amanda J. Casella; Dean R. Peterman; Samuel A. Bryan

2013-12-01T23:59:59.000Z

86

Fourier Transform Infrared Spectroscopy and Multivariate Analysis for Online Monitoring of Dibutyl Phosphate Degradation Product in Tributyl Phosphate /n-Dodecane/Nitric Acid Solvent  

SciTech Connect (OSTI)

In liquid-liquid extraction separation processes, accumulation of organic solvent degradation products is detrimental to the process robustness and frequent solvent analysis is warranted. Our research explores feasibility of online monitoring of the organic solvents relevant to used nuclear fuel reprocessing. This paper describes the first phase of developing a system for monitoring the tributyl phosphate (TBP)/n-dodecane solvent commonly used to separate used nuclear fuel. In this investigation, the effect of extraction of nitric acid from aqueous solutions of variable concentrations on the quantification of TBP and its major degradation product dibutyl phosphoric acid (HDBP) was assessed. Fourier Transform Infrared Spectroscopy (FTIR) spectroscopy was used to discriminate between HDBP and TBP in the nitric acid-containing TBP/n-dodecane solvent. Multivariate analysis of the spectral data facilitated the development of regression models for HDBP and TBP quantification in real time, enabling online implementation of the monitoring system. The predictive regression models were validated using TBP/n-dodecane solvent samples subjected to the high dose external gamma irradiation. The predictive models were translated to flow conditions using a hollow fiber FTIR probe installed in a centrifugal contactor extraction apparatus demonstrating the applicability of the FTIR technique coupled with multivariate analysis for the online monitoring of the organic solvent degradation products.

Levitskaia, Tatiana G.; Peterson, James M.; Campbell, Emily L.; Casella, Amanda J.; Peterman, Dean; Bryan, Samuel A.

2013-11-05T23:59:59.000Z

87

Novel Regenerated Solvent Extraction Processes for the Recovery of Carboxylic Acids or Ammonia from Aqueous Solutions Part I. Regeneration of Amine-Carboxylic Acid Extracts  

SciTech Connect (OSTI)

Two novel regenerated solvent extraction processes are examined. The first process has the potential to reduce the energy costs inherent in the recovery of low-volatility carboxylic acids from dilute aqueous solutions. The second process has the potential for reducing the energy costs required for separate recovery of ammonia and acid gases (e.g. CO{sub 2} and H{sub 2}S) from industrial sour waters. The recovery of carboxylic acids from dilute aqueous solution can be achieved by extraction with tertiary amines. An approach for regeneration and product recovery from such extracts is to back-extract the carboxylic acid with a water-soluble, volatile tertiary amine, such as trimethylamine. The resulting trimethylammonium carboxylate solution can be concentrated and thermally decomposed, yielding the product acid and the volatile amine for recycle. Experimental work was performed with lactic acid, succinic acid, and fumaric acid. Equilibrium data show near-stoichiometric recovery of the carboxylic acids from an organic solution of Alamine 336 into aqueous solutions of trimethylamine. For fumaric and succinic acids, partial evaporation of the aqueous back extract decomposes the carboxylate and yields the acid product in crystalline form. The decomposition of aqueous solutions of trimethylammonium lactates was not carried out to completion, due to the high water solubility of lactic acid and the tendency of the acid to self-associate. The separate recovery of ammonia and acid gases from sour waters can be achieved by combining steam-stripping of the acid gases with simultaneous removal of ammonia by extraction with a liquid cation exchanger. The use of di-2,4,4-trimethylpentyl phosphinic acid as the liquid cation exchanger is explored in this work. Batch extraction experiments were carried out to measure the equilibrium distribution ratio of ammonia between an aqueous buffer solution and an organic solution of the phosphinic acid (0.2N) in Norpar 12. The concentration-based distribution ratios increase from 0.11 to 0.46 as the aqueous phase pH increases from 7.18 to 8.15. Regeneration of the organic extractant solution was carried out by stripping at elevated temperatures to remove the ammonia, with 99% recovery of the ammonia being obtained at 125 C.

Poole, L.J.; King, C.J.

1990-03-01T23:59:59.000Z

88

Process for the recovery of uranium from wet-process phosphoric acid  

SciTech Connect (OSTI)

In a process for the recovery of uranium from a wet-process phosphoric acid, comprising treating in an extraction step the preliminarily oxidized acid first with an organic solvent consisting essentially of a dialkylphosphoric acid and a trialkyphosphine oxide dissolved in an inert and unreactive organic solvent whereby there are obtained a uranium-free phosphoric acid and an organic extract consisting essentially of the solvent containing the major portion of uranium; then, in a reextraction step, separating the uranium from the organic extract as ammonium uranyl tricarbonate by reacting the organic extract with ammonium hydroxide and ammonium carbonate; and recycling the uranium-free solvent to the extraction step; an improvement comprises treating the organic extract in a reextraction apparatus having at least two stages, by (A) introducing the extract at the head of the first stage; (B) countercurrently introducing ammonia or ammonium hydroxide solution at the bottom of the first stage; the ph of the first stage being controlled and maintained at a value of 8.0 to 8.5; (C) introducing an ammonium carbonate aqueous solution at the bottom of the last stage; the amount of ammonium carbonate employed being 50-80 percent by weight of the theoretical molar quantity which is necessary to neutralize the dialkylphosphoric acid contained in the solvent and to convert the uranium to ammonium uranyl tricarbonate; and (D) regenerating the ammoniated solvent obtained after the reextraction step by treating it with an acid before recycling it to the extraction step.

Francois, A.; Sialino, A.

1980-12-09T23:59:59.000Z

89

Salt Effect Model for Aqueous Solubility of TBP in a 5 to 100% TBP/n-Dodecane-Nitric Acid-Water Biphasic System at 298.2 K  

SciTech Connect (OSTI)

The solubilities of nonelectrolytes in aqueous electrolyte solutions have traditionally been modeled by using the Setschenow equation for salt effect. The aqueous solubility of tri-n-butyl phosphate (TBP) during operating conditions of the Purex process is an important parameter for safety considerations. Use of the Setschenow equation for aqueous solubility of TBP under limited conditions has been reported in the literature. However, there is no general model available to account for the presence of the diluent and for the case of multicomponent electrolyte solutions in which only some electrolytes are solvated and extracted by TBP. An extended salt effect model is proposed for predicting the aqueous solubility of TBP in a 5 to 100% TBP/n-dodecane-nitric acid-water biphasic system at 298.2 K. The literature data on TBP solubility were correlated to aqueous acid concentration, diluent concentration in the solvents, and an interaction parameter for electrolytic solutes (extracted or not extracted by TBP)

Kumar, Shekhar; Koganti, Sudhir Babu [Indira Gandhi Centre for Atomic Research (India)

2000-02-15T23:59:59.000Z

90

Modeling of the simultaneous extraction of nitric acid and uranyl nitrate with tri-n-butyl phosphate. Application to extraction operation  

SciTech Connect (OSTI)

A mathematical model developed for the equilibrium HNO{sub 3}-UO{sub 2}(NO{sub 3}){sub 2}-tri-n-butyl phosphate (TBP)-diluent is the basis of the computation of distribution isotherms. The isotherms are used to study the influence of TBP concentration on two chosen operation parameters, distribution coefficients and number of theoretical stages, for the selected flow sheets. It is established that an increase in TBP concentration leads to a decrease in the number of theoretical stages for the extraction flow sheets but to their increase for the striping flow sheets. Given diagrams can be used to determine the efficiency of extraction processes. Agreement with available literature calculations on the number of theoretical stages supports the use of the model in the computation of distribution isotherms, of the system quoted above, in a wide range of nitric acid, uranyl nitrate, and TBP concentrations.

Comor, J.J.; Tolic, A.S.; Kopecni, M.M.; Petkovic, D.M. [Vinca Inst. of Nuclear Sciences, Belgrade (Yugoslavia). Chemical Dynamics Lab.] [Vinca Inst. of Nuclear Sciences, Belgrade (Yugoslavia). Chemical Dynamics Lab.

1999-01-01T23:59:59.000Z

91

Electrode Induced Removal and Recovery of Uranium (VI) from Acidic Subsurfaces  

SciTech Connect (OSTI)

The overarching objective of this research is to provide an improved understanding of how aqueous geochemical conditions impact the removal of U and Tc from groundwater and how engineering design may be utilized to optimize removal of these radionuclides. Experiments were designed to address the unique conditions in Area 3 of ORNL while also providing broader insight into the geochemical effectors of the removal rates and extent for U and Tc. The specific tasks of this work were to: 1) quantify the impact of common aqueous geochemical and operational conditions on the rate and extent of U removal and recovery from water, 2) investigate the removal of Tc with polarized graphite electrode, and determine the influence of geochemical and operational conditions on Tc removal and recovery, 3) determine whether U and Tc may be treated simultaneous from Area 3 groundwater, and examine the bench-scale performance of electrode-based treatment, and 4) determine the capacity of graphite electrodes for U(VI) removal and develop a mathematical, kinetic model for the removal of U(VI) from aqueous solution. Overall the body of work suggests that an electrode-based approach for the remediation of acidic subsurface environments, such as those observed in Area 3 of ORNL may be successful for the removal for both U(VI) and Tc. Carbonaceous (graphite) electrode materials are likely to be the least costly means to maximize removal rates and efficiency by maximizing the electrode surface area.

Gregory, Kelvin [Carnegie Mellon University

2013-08-12T23:59:59.000Z

92

E-Print Network 3.0 - ambient nitric oxide Sample Search Results  

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

oxides (NOx)." Other nitrogen oxides include nitrous acid and nitric acid. While... . Nitrogen Dioxide: Nitrogen dioxide (NO2) is one of a group of highly reactive gasses known...

93

The Effect of Acid Additives on Carbonate Rock Wettability and Spent Acid Recovery in Low Permeability Gas Carbonates  

E-Print Network [OSTI]

Spent acid retention in the near-wellbore region causes reduction of relative permeability to gas and eventually curtailed gas production. In low-permeability gas carbonate reservoirs, capillary forces are the key parameters that affect the trapping...

Saneifar, Mehrnoosh

2012-10-19T23:59:59.000Z

94

From Acid Dip to Thriving Waters The Impact of Emissions Reductions on Lake Recovery  

E-Print Network [OSTI]

-Range Transboundary Air Pollution for various pollutants including sulphur dioxide (SO2), nitrogen oxides (NOx countries implementing domestic regula- tions to control emissions of pollutants. While the problems October 1, 2007 Abstract We develop an optimal control model for the recovery of a representative

Sadoulet, Elisabeth

95

Zinc recovery by ultrasound acid leaching of double kiln treated electric arc furnace dust  

SciTech Connect (OSTI)

The need to convert 70,000 tons a year of electric arc furnace (EAF) dust into an environmentally safe or recyclable product has encouraged studies to reclaim zinc from this waste material. Successful characterization of a double-kiln calcine, produced from EAF dust, has shown that the calcine pellets consisted mainly of zinc oxide plates with some iron oxide particles. Preliminary leaching tests using hydrochloric and sulfuric acids indicated that this calcine is suitable for selective ultrasound leaching of zinc. A factorially designed screening test using hydrochloric acid showed that ultrasound significantly lowered iron dissolution and increased zinc dissolution, thus enhancing the selective leaching of zinc. Ultrasound, temperature, air bubbling rate and acidity increased the sulfuric acid selectivity, while fluorosilicic acid was not selective. Reactor characterization through ultrasonic field measurements led to the selection of reactor and ultrasound bath, which were utilized to enhance the selectivity of a laboratory scale sulfuric acid leaching of a double-kiln treated electric arc furnace dust. Results indicated that ultrasonic leaching of this calcine is a satisfactory technique to selectively separate zinc from iron. After further iron removal by precipitation and cementation of nickel, it was possible to electrowin zinc from the leach liquor under common industrial conditions, with current efficiencies from 86% through 92% being observed. Calcine washing showed that a substantial chloride removal is possible, but fluoride ion in the electrolyte caused deposit sticking during electrowinning.

Barrera Godinez, J.A.

1989-01-01T23:59:59.000Z

96

Recovery of carboxylic acids at pH greater than pK{sub a}  

SciTech Connect (OSTI)

Economics of producing carboxylic acids by fermentation is often dominated, not by the fermentation cost, but by the cost of recovering and purifying the acids from dilute aqueous solutions. Experiments were performed to measure uptakes of lactic and succinic acids as functions of pH by basic polymeric sorbents; sorbent regeneration was also tested. Performance at pH > pK{sub a} and regenerability depend on sorbent basicity; apparent pK{sub a} and monomer pK{sub a} can be used to predict sorbent performance. Two basic amine extractants, Alamine 336 and Amberlite LA-2, in were also studied; they are able to sustain capacity to higher pH in diluents that stabilize the acid-amine complex through H bonding. Secondary amines perform better than tert-amines in diluents that solvate the additional proton. Competitive sulfate and phosphate, an interference in fermentation, are taken up by sorbents more strongly than by extractants. The third step in the proposed fermentation process, the cracking of the trimethylammonium (TMA) carboxylate, was also examined. Because lactic acid is more soluble and tends to self-esterify, simple thermal cracking does not remove all TMA; a more promising approach is to esterify the TMA lactate by reaction with an alcohol.

Tung, L.A.

1993-08-01T23:59:59.000Z

97

Reactions Between Water Soluble Organic Acids and Nitrates in...  

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

Reactions Between Water Soluble Organic Acids and Nitrates in Atmospheric Aerosols: Recycling of Nitric Acid and Formation of Reactions Between Water Soluble Organic Acids and...

98

Remedial Investigation Report on the Abandoned Nitric Acid Pipeline at the Oak Ridge Y-12 Plant, Oak Ridge, Tennessee. Energy Systems Environmental Restoration Program; Y-12 Environmental Restoration Program  

SciTech Connect (OSTI)

Upper East Fork Poplar Creek Operable Unit 2 consists of the Abandoned Nitric Acid pipeline (ANAP). This pipeline was installed in 1951 to transport liquid wastes {approximately}4800 ft from Buildings 9212, 9215, and 9206 to the S-3 Ponds. Materials known to have been discharged through the pipeline include nitric acid, depleted and enriched uranium, various metal nitrates, salts, and lead skimmings. During the mid-1980s, sections of the pipeline were removed during various construction projects. A total of 19 locations were chosen to be investigated along the pipeline for the first phase of this Remedial Investigation. Sampling consisted of drilling down to obtain a soil sample at a depth immediately below the pipeline. Additional samples were obtained deeper in the subsurface depending upon the depth of the pipeline, the depth of the water table, and the point of auger refusal. The 19 samples collected below the pipeline were analyzed by the Oak Ridge Y-12 Plant`s laboratory for metals, nitrate/nitrite, and isotopic uranium. Samples collected from three boreholes were also analyzed for volatile organic compounds because these samples produced a response with organic vapor monitoring equipment. Uranium activities in the soil samples ranged from 0.53 to 13.0 pCi/g for {sup 238}U, from 0.075 to 0.75 pCi/g for {sup 235}U, and from 0.71 to 5.0 pCi/g for {sup 238}U. Maximum total values for lead, chromium, and nickel were 75.1 mg/kg, 56.3 mg/kg, and 53.0 mg/kg, respectively. The maximum nitrate/nitrite value detected was 32.0 mg-N/kg. One sample obtained adjacent to a sewer line contained various organic compounds, at least some of which were tentatively identified as fragrance chemicals commonly associated with soaps and cleaning solutions. The results of the baseline human health risk assessment for the ANAP contaminants of potential concern show no unacceptable risks to human health.

Not Available

1994-02-01T23:59:59.000Z

99

Process for the extraction of strontium from acidic solutions  

DOE Patents [OSTI]

The invention is a process for selectively extracting strontium values from aqueous nitric acid waste solutions containing these and other fission product values. The extractant solution is a macrocyclic polyether in an aliphatic hydrocarbon diluent containing a phase modifier. The process will selectively extract strontium values from nitric acid solutions which are up to 6 molar in nitric acid.

Horwitz, E. Philip (Naperville, IL); Dietz, Mark L. (Evanston, IL)

1994-01-01T23:59:59.000Z

100

Process for the extraction of strontium from acidic solutions  

DOE Patents [OSTI]

The invention is a process for selectively extracting strontium values from aqueous nitric acid waste solutions containing these and other fission product values. The extractant solution is a macrocyclic polyether in an aliphatic hydrocarbon diluent containing a phase modifier. The process will selectively extract strontium values from nitric acid solutions which are up to 6 molar in nitric acid.

Horwitz, E.P.; Dietz, M.L.

1993-01-01T23:59:59.000Z

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


101

Process for the extraction of strontium from acidic solutions  

DOE Patents [OSTI]

The invention is a process for selectively extracting strontium values from aqueous nitric acid waste solutions containing these and other fission product values. The extractant solution is a macrocyclic polyether in an aliphatic hydrocarbon diluent containing a phase modifier. The process will selectively extract strontium values from nitric acid solutions which are up to 6 molar in nitric acid. 4 figs.

Horwitz, E.P.; Dietz, M.L.

1994-09-06T23:59:59.000Z

102

E-Print Network 3.0 - ammonia acetic acid Sample Search Results  

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

fluminic acid, or hydrogen. NITRIC ACID with: acetic... with: water, carbon dioxide, carbon tetrachloride, and other chlorinated hydrocarbons. ACETIC ACID with......

103

E-Print Network 3.0 - acid alkyl esters Sample Search Results  

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

Nitric Acid 34. Sulfuric acid... .5 will not be accepted through this program. Heavy metal, toxic, acidic (without solvents) and basic wastes should... . Mercaptans 4. ......

104

Solvent extraction and recovery of the transuranic elements from waste solutions using the TRUEX process  

SciTech Connect (OSTI)

High-level liquid waste is produced during the processing of irradiated nuclear fuel by the PUREX process. In some cases the treatment of metallurgical scrap to recover the plutonium values also generates a nitric acid waste solution. Both waste solutions contain sufficient concentrations of transuranic elements (mostly /sup 241/Am) to require handling and disposal as a TRU waste. This paper describes a recently developed solvent extraction/recovery process called TRUEX (transuranium extraction) which is designed to reduce the TRU concentration in nitric waste solutions to <100 nCi/g of disposed form (1,2). (In the USA, non-TRU waste is defined as <100 nCi of TRU/g of disposed form.) The process utilizes PUREX process solvent (TBP in a normal paraffinic hydrocarbon or carbon tetrachloride) modified by a small concentration of octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (abbrev. CMPO). The presence of CMPO enables the modified PUREX process solvent to extract trivalent actinides as well as tetra- and hexavalent actinides. A major feature of the TRUEX process is that is is applicable to waste solutions containing a wide range of nitric acid, salt, and fission product concentrations and at the same time is very compatible with existing liquid-liquid extraction technology as usually practiced in a fuel reprocessing plant. To date the process has been tested on two different types of synthetic waste solutions. The first solution is a typical high-level nitric acid waste and the second a typical waste solution generated in metallurgical scrap processing. Results are discussed. 4 refs., 1 fig., 4 tabs.

Horwitz, E.P.; Schulz, W.W.

1985-01-01T23:59:59.000Z

105

acid docosahexaenoic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 38 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

106

acid aspartic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 20 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

107

acid caffeic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 11 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

108

acid benzoic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 24 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

109

acid propanoic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 9 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

110

acid oleic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 31 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

111

Process for the recovery of curium-244 from nuclear waste  

SciTech Connect (OSTI)

A process has been designed for the recovery of curium from purex waste. Curium and americium are separated from the lanthanides by a TALSPEAK extraction process using differential extraction. Equations were derived for the estimation of the economically optimum conditions for the extraction using laboratory batch extraction data. The preparation of feed for the extraction involves the removal of nitric acid from the Purex waste by vaporization under reduced pressure, the leaching of soluble nitrates from the resulting cake, and the oxalate precipitation of a pure lanthanide-actinide fraction. Final separation of the curium from americium is done by ion-exchange. The steps of the process, except ion-exchange, were tested on a laboratory scale and workable conditions were determined.

Posey, J.C.

1980-10-01T23:59:59.000Z

112

Efficient recovery of nano-sized iron oxide particles from synthetic acid-mine drainage (AMD) water using fuel cell  

E-Print Network [OSTI]

, Hangzhou 310027, PR China b Department of Civil and Environmental Engineering, 212 Sackett Building, Penn (AMD) is an important contributor to surface water pollution due to the release of acid and metals. Fe chemicals such as lead, copper, cadmium, and arsenic. AMD can be difficult and costly to treat. Treatment

113

acidization: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 7 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

114

acid-dependent ribonucleic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 40 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

115

Controlling acid rain  

E-Print Network [OSTI]

High concentrations of sulfuric and nitric acid in raTn fn the northeastern USA are caused by the large scale combustion of fossil fuels within this region. Average precipitation acidity is pH 4.2, but spatial and temporal ...

Fay, James A.

1983-01-01T23:59:59.000Z

116

Power Recovery  

E-Print Network [OSTI]

.POWER RECOVERY Fletcher Mlirray Monsanto Chemical Company AB5'-:::0 p.p., will ??vi.w 'h. '.ohnnln,y nf 'h.::v,n. T:X:~~T ~ methods for estimating the power recovery potential from fluid streams. The ideal gas law formula for expanding gases.... Gas Law Estimation Power recovery estimates from a vapor stream can be made using the formula: which is derived from the Ideal Gas Law. At first glance the. formula seems imposing and perhaps difficult to occasionally use. If however; the formula...

Murray, F.

117

Recovery Act  

Broader source: Energy.gov [DOE]

Recovery Act and Energy Department programs were designed to stimulate the economy while creating new power sources, conserving resources and aligning the nation to once again lead the global energy economy.

118

acid mononucleotide adenylyltransferase: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 14 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

119

aminoadipic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 7 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

120

aminocaproic acid eaca: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 7 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

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


121

acid hydrazone dpktch: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 11 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

122

aminolevulinic acid dehydratase: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 18 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

123

aminobutyric acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 36 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

124

acid controls expression: Topics by E-print Network  

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

12 13 14 15 16 17 18 19 20 21 22 23 24 25 Next Page Last Page Topic Index 1 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

125

aminolevulinic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 12 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

126

acid riboside salvage: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 30 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

127

anf 4-hydroxyhomocitric acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 15 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

128

acid dioxygenase hpd: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 37 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

129

acid ascorbyl palmitate: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 27 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

130

acid dehydratase alad: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 15 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

131

acetoacetic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 8 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

132

acid lna taqman: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 46 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

133

amygdalic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 8 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

134

acid phosphoribosyltransferase 1-deficient: Topics by E-print...  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 19 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

135

adipic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 11 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

136

acid dmsa renography: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 8 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

137

anthranilic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 10 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

138

aminocaproic acids: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 7 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

139

acid glycosaminoglycan mucopolysaccharide: Topics by E-print...  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 34 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

140

acidic oligosaccharides paos: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 40 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

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


141

aminobutyric acids: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 36 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

142

asparaginic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 17 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

143

arsonic acids: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 10 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

144

anthraquinonic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 12 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

145

aristolochic acid nephropathy: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 28 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

146

acetylsalicylic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 11 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

147

acid decarboxylase hgad65: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 32 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

148

Solvent extraction of inorganic acids  

E-Print Network [OSTI]

the solution by a sim?. le process that is economically =ttrsctlve is of con- sider. ble interest~ Dilute "olution; of hydrochloric, nitric and sul- furic acid d; occur in many processes either alone or toga- th: r . 'he use of li. , uid-li~uid extraction...~~ram for hexyl c~rbitol- water-nitric acid 17 ~ Distribution die, r m for hoxl'' ca:-bitol- watcr-sulfur'c acid Table 1. . 'xperimental d ta of amyl alcohol-water-!!Cl Pa, e 33 2. Experimental data of isoamyl alcohol-water- HC1 34 3 ~ Cxperimental data...

Ysrael, Miguel Curie

1965-01-01T23:59:59.000Z

149

Recovery Act: State Assistance for Recovery Act Related Electricity...  

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

Center Recovery Act Recovery Act: State Assistance for Recovery Act Related Electricity Policies Recovery Act: State Assistance for Recovery Act Related Electricity...

150

Process for combined control of mercury and nitric oxide.  

SciTech Connect (OSTI)

Continuing concern about the effects of mercury in the environment may lead to requirements for the control of mercury emissions from coal-fired power plants. If such controls are mandated, the use of existing flue-gas cleanup systems, such as wet scrubbers currently employed for flue-gas desulfurization, would be desirable, Such scrubbers have been shown to be effective for capturing oxidized forms of mercury, but cannot capture the very insoluble elemental mercury (Hg{sup 0}) that can form a significant fraction of the total emissions. At Argonne National Laboratory, we have proposed and tested a concept for enhancing removal of Hg{sup 0}, as well as nitric oxide, through introduction of an oxidizing agent into the flue gas upstream of a scrubber, which readily absorbs the soluble reaction products. Recently, we developed a new method for introducing the oxidizing agent into the flue-gas stream that dramatically improved reactant utilization. The oxidizing agent employed was NOXSORB{trademark}, which is a commercial product containing chloric acid and sodium chlorate. When a dilute solution of this agent was introduced into a gas stream containing Hg{sup 0} and other typical flue-gas species at 300 F, we found that about 100% of the mercury was removed from the gas phase and recovered in process liquids. At the same time, approximately 80% of the nitric oxide was removed. The effect of sulfur dioxide on this process was also investigated and the results showed that it slightly decreased the amount of Hg{sup 0} oxidized while appearing to increase the removal of nitric oxide from the gas phase. We are currently testing the effects of variations in NOXSORB{trademark} concentration, sulfur dioxide concentration, nitric oxide concentration, and reaction time (residence time). Preliminary economic projections based on the results to date indicate that the chemical cost for nitric oxide oxidation could be less than $5,000/ton removed, while for Hg{sup 0} oxidation it would be about $20,000/lb removed.

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

1999-11-03T23:59:59.000Z

151

Process for recovery of palladium from nuclear fuel reprocessing wastes  

DOE Patents [OSTI]

Palladium is selectively removed from spent nuclear fuel reprocessing waste by adding sugar to a strong nitric acid solution of the waste to partially denitrate the solution and cause formation of an insoluble palladium compound. The process includes the steps of: (a) adjusting the nitric acid content of the starting solution to about 10 M; (b) adding 50% sucrose solution in an amount sufficient to effect the precipitation of the palladium compound; (c) heating the solution at reflux temperature until precipitation is complete; and (d) centrifuging the solution to separate the precipitated palladium compound from the supernatant liquid.

Campbell, D.O.; Buxton, S.R.

1980-06-16T23:59:59.000Z

152

Bulk liquid membrane for the recovery of chromium(VI) from a hydrochloric acid medium using dicyclohexano-18-crown-6 as extractant-carrier  

SciTech Connect (OSTI)

The solvent extraction and transfer of chromic acid from hydrochloric acid medium through a bulk liquid membrane containing dicyclohexano-18-crown-6 (L) were studied. Extraction experiments pointed out that chromium(VI) was coextracted with the chloride ion which formed the complex ion pair L(H{sub 3}O{sup +})CrO{sub 3}Cl{sup {minus}} in the organic phase. The Donnan equilibrium isotherm based on the extraction, stripping, and CrO{sub 3}Cl{sup {minus}} hydrolysis equilibria allowed prediction of the performance of the semipermeable membrane to concentrate chlorochromic acid in the receiving phase. Transport experiments confirmed the ability of the liquid membrane to recover chlorochromic acid in pure water. The transport kinetics was modeled by using the two-film theory applied to the liquid membrane.

Zouhri, A. [Univ. Ibnou Zohr, Agadir (Morocco). Faulte de Sciences] [Univ. Ibnou Zohr, Agadir (Morocco). Faulte de Sciences; Ernst, B.; Burgard, M. [Ecole Europeenne de Chimie, Polymeres et Materiaux, Strasbourg (France)] [Ecole Europeenne de Chimie, Polymeres et Materiaux, Strasbourg (France)

1999-06-01T23:59:59.000Z

153

Leaching studies for tin recovery from waste e-scrap  

SciTech Connect (OSTI)

Printed circuit boards (PCBs) are the most essential components of all electrical and electronic equipments, which contain noteworthy quantity of metals, some of which are toxic to life and all of which are valuable resources. Therefore, recycling of PCBs is necessary for the safe disposal/utilization of these metals. Present paper is a part of developing Indo-Korean recycling technique consists of organic swelling pre-treatment technique for the liberation of thin layer of metallic sheet and the treatment of epoxy resin to remove/recover toxic soldering material. To optimize the parameters required for recovery of tin from waste PCBs, initially the bench scale studies were carried out using fresh solder (containing 52.6% Sn and 47.3% Pb) varying the acid concentration, temperature, mixing time and pulp density. The experimental data indicate that 95.79% of tin was leached out from solder material using 5.5 M HCl at fixed pulp density 50 g/L and temperature 90 Degree-Sign C in mixing time 165 min. Kinetic studies followed the chemical reaction controlled dense constant size cylindrical particles with activation energy of 117.68 kJ/mol. However, 97.79% of tin was found to be leached out from solder materials of liberated swelled epoxy resin using 4.5 M HCl at 90 Degree-Sign C, mixing time 60 min and pulp density 50 g/L. From the leach liquor of solder materials of epoxy resin, the precipitate of sodium stannate as value added product was obtained at pH 1.9. The Pb from the leach residue was removed by using 0.1 M nitric acid at 90 Degree-Sign C in mixing time 45 min and pulp density 10 g/L. The metal free epoxy resin could be disposed-of safely/used as filling material without affecting the environment.

Jha, Manis Kumar, E-mail: maniskrjha@gmail.com [Metal Extraction and Forming Division, National Metallurgical Laboratory (NML), Jamshedpur 831 007 (India); Choubey, Pankaj Kumar; Jha, Amrita Kumari; Kumari, Archana [Metal Extraction and Forming Division, National Metallurgical Laboratory (NML), Jamshedpur 831 007 (India); Lee, Jae-chun, E-mail: jclee@kigam.re.kr [Mineral Resources Research Division, Korea Institute of Geosciences and Mineral Resources, Daejeon 305-350 (Korea, Republic of); Kumar, Vinay [Metal Extraction and Forming Division, National Metallurgical Laboratory (NML), Jamshedpur 831 007 (India); Jeong, Jinki [Mineral Resources Research Division, Korea Institute of Geosciences and Mineral Resources, Daejeon 305-350 (Korea, Republic of)

2012-10-15T23:59:59.000Z

154

acidic pathogenesis-related pr-1: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 23 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

155

alpha-amino-isobutyric acid aib: Topics by E-print Network  

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

12 13 14 15 16 17 18 19 20 21 22 23 24 25 Next Page Last Page Topic Index 21 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

156

acid o-methyltransferase activity1: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 39 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

157

alpha-oxo acid decarboxylase: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 32 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

158

anti-psoriatic fumaric acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 15 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

159

alpha2-6-linked sialic acid: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 33 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

160

anti-proliferative acidic meglcua: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 12 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

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


161

abscisic acid receptor1oa: Topics by E-print Network  

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

by USDA and U of I researchers Illinois at Urbana-Champaign, University of 44 Controlling acid rain MIT - DSpace Summary: High concentrations of sulfuric and nitric acid in raTn fn...

162

Ovarian nitric oxide synthase gene expression during peripubertal development  

E-Print Network [OSTI]

Nitric oxide (NO) is generated from L-arginine by different isoforms of the enzyme nitric oxide synthase. (NOS) and is known to be involved in mediating several biological functions, some of which are associated with reproduction. Much attention...

Jones, Benjamin James

1997-01-01T23:59:59.000Z

163

Mechanism of Nitric Oxide Reactivity and Fluorescence Enhancement of the NO-Specific Probe CuFL1  

E-Print Network [OSTI]

The mechanism of the reaction of CuFL1 (FL1 = 2-{2-chloro-6-hydroxy-5-[(2-methylquinolin-8-ylamino)methyl]-3-oxo-3H-xanthen-9-yl}benzoic acid) with nitric oxide (NO) to form the N-nitrosated product FL1-NO in buffered ...

McQuade, Lindsey E.

164

Recovery FAQ - Hanford Site  

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

Recovery Act of 2009 > Hanford ARRA FAQ Recovery Act of 2009 Hanford ARRA FAQ Hanford ARRA Weekly Reports Hanford ARRA News Hanford ARRA Photogallery Hanford ARRA Videos Hanford...

165

Atomistic Oxidation of a Carbon Nanotube in Nitric Acid  

E-Print Network [OSTI]

PRL 104, 066401 (2010) PHYSICAL REVIEW LETTERS week endingAmerican Physical Society PRL 104, 066401 (2010) PHYSICALthese conditions, the en- PRL 104, 066401 (2010) PHYSICAL

Collins, Philip G

2010-01-01T23:59:59.000Z

166

Active Phosphoric Acid and Its Relation to the Needs of the Soil for Phosphoric Acid in Pot Experiments.  

E-Print Network [OSTI]

. K/5 nitric acid, measured with a flask. Place in ter bath previously heated to 40" C. Digest five hours, shak- ?very half hour. Filter on a large'double folded filter. When cola, take 1800 c.c. for the estimation of phosphoric acid and potael... and silica. The filtrate was measured ancl its vol- ume recorded. The soil on the filter paper was washed back into the bottle with 2000 c.c. N,'5 nitric acid, and again digested. Fonr treatments in all were made with the acid, The quantity of phosphorjc...

Fraps, G. S. (George Stronach)

1909-01-01T23:59:59.000Z

167

Locating Heat Recovery Opportunities  

E-Print Network [OSTI]

Basic concepts of heat recovery are defined as they apply to the industrial community. Methods for locating, ranking, and developing heat recovery opportunities are presented and explained. The needs for useful heat 'sinks' are emphasized as equal...

Waterland, A. F.

1981-01-01T23:59:59.000Z

168

Recovery Act Milestones  

ScienceCinema (OSTI)

Every 100 days, the Department of Energy is held accountable for a progress report on the American Recovery and Reinvestment Act. Update at 200 days, hosted by Matt Rogers, Senior Advisor to Secretary Steven Chu for Recovery Act Implementation.

Rogers, Matt

2013-05-29T23:59:59.000Z

169

Waste Steam Recovery  

E-Print Network [OSTI]

applicable to other sources of steam. The interaction of the recovery system with the plant's steam/power system has been included. Typical operating economics have been prepared. It was found that the profitability of most recovery schemes is generally...

Kleinfeld, J. M.

1979-01-01T23:59:59.000Z

170

Synthesis and development of processes for the recovery of sulfur from acid gases. Part 1, Development of a high-temperature process for removal of H{sub 2}S from coal gas using limestone -- thermodynamic and kinetic considerations; Part 2, Development of a zero-emissions process for recovery of sulfur from acid gas streams  

SciTech Connect (OSTI)

Limestone can be used more effectively as a sorbent for H{sub 2}S in high-temperature gas-cleaning applications if it is prevented from undergoing calcination. Sorption of H{sub 2}S by limestone is impeded by sintering of the product CaS layer. Sintering of CaS is catalyzed by CO{sub 2}, but is not affected by N{sub 2} or H{sub 2}. The kinetics of CaS sintering was determined for the temperature range 750--900{degrees}C. When hydrogen sulfide is heated above 600{degrees}C in the presence of carbon dioxide elemental sulfur is formed. The rate-limiting step of elemental sulfur formation is thermal decomposition of H{sub 2}S. Part of the hydrogen thereby produced reacts with CO{sub 2}, forming CO via the water-gas-shift reaction. The equilibrium of H{sub 2}S decomposition is therefore shifted to favor the formation of elemental sulfur. The main byproduct is COS, formed by a reaction between CO{sub 2} and H{sub 2}S that is analogous to the water-gas-shift reaction. Smaller amounts of SO{sub 2} and CS{sub 2} also form. Molybdenum disulfide is a strong catalyst for H{sub 2}S decomposition in the presence of CO{sub 2}. A process for recovery of sulfur from H{sub 2}S using this chemistry is as follows: Hydrogen sulfide is heated in a high-temperature reactor in the presence of CO{sub 2} and a suitable catalyst. The primary products of the overall reaction are S{sub 2}, CO, H{sub 2} and H{sub 2}O. Rapid quenching of the reaction mixture to roughly 600{degrees}C prevents loss Of S{sub 2} during cooling. Carbonyl sulfide is removed from the product gas by hydrolysis back to CO{sub 2} and H{sub 2}S. Unreacted CO{sub 2} and H{sub 2}S are removed from the product gas and recycled to the reactor, leaving a gas consisting chiefly of H{sub 2} and CO, which recovers the hydrogen value from the H{sub 2}S. This process is economically favorable compared to the existing sulfur-recovery technology and allows emissions of sulfur-containing gases to be controlled to very low levels.

Towler, G.P.; Lynn, S.

1993-05-01T23:59:59.000Z

171

acute nitric oxide: Topics by E-print Network  

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

with a genetic polymorphisms in nitric oxide synthase genes (NOS), a higher nicotine exposure was associated with lower FeNO levels. Finally, although more studies are needed...

172

Nitric oxide reactions of bio-Inspired zinc and cobalt complexes  

E-Print Network [OSTI]

Chapter 1. Bioinorganic Chemistry of Nitric Oxide and of Some of Its Targets The redox-active nature of nitric oxide (NO) regulates the chemistry and roles of NO in biology. The interactions of NO with nitric oxide synthases, ...

Kozhukh, Julia, 1985-

2012-01-01T23:59:59.000Z

173

Relation of the Water-Soluble Potash, the Replaceable and Acid-Soluble Potash to the Potash Removed by Crops in Pot Experiments.  

E-Print Network [OSTI]

ammonia. This acid is 3.33 N. Digest 10 grams soil for 24 hours with 100 c.c. of the above hydrochloric acid at room temperature, shaking occasionally. Filter and wash with hot water. Add 1 c.c. nitric acid. Evaporate to dryness and heat on steam bath... of the soil with nitric acid become greater as the potash taken up by crops increases. Correlation coefficients for the factors studied show close relations between them. Correction of the 0.2N nitric acid for neutralization by the bases of the soil...

Fraps, G. S. (George Stronach)

1929-01-01T23:59:59.000Z

174

Response of shoot growth and gas exchange of Picea abies clones to rain acidity  

E-Print Network [OSTI]

Response of shoot growth and gas exchange of Picea abies clones to rain acidity and the addition, particularly the effect of acidity and the addition of a realistic ionic mixture to simulated acidic.0 with a mixture of sulfuric and nitric acids (S02-/NO-weight ratio = 2.4). Ionic concentrations m mg/1were: 4.50 S

Paris-Sud XI, Université de

175

Battleground Energy Recovery Project  

SciTech Connect (OSTI)

In October 2009, the project partners began a 36-month effort to develop an innovative, commercial-scale demonstration project incorporating state-of-the-art waste heat recovery technology at Clean Harbors, Inc., a large hazardous waste incinerator site located in Deer Park, Texas. With financial support provided by the U.S. Department of Energy, the Battleground Energy Recovery Project was launched to advance waste heat recovery solutions into the hazardous waste incineration market, an area that has seen little adoption of heat recovery in the United States. The goal of the project was to accelerate the use of energy-efficient, waste heat recovery technology as an alternative means to produce steam for industrial processes. The project had three main engineering and business objectives: Prove Feasibility of Waste Heat Recovery Technology at a Hazardous Waste Incinerator Complex; Provide Low-cost Steam to a Major Polypropylene Plant Using Waste Heat; and ï?· Create a Showcase Waste Heat Recovery Demonstration Project.

Daniel Bullock

2011-12-31T23:59:59.000Z

176

E-Print Network 3.0 - actual nitric oxide Sample Search Results  

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

combustion are nitric oxide (NO) and nitrogen... of the nitric oxide is oxidized to nitrogen dioxide, so the environmental effects of emissions of both... O emissions at coal...

177

E-Print Network 3.0 - affects nitric oxide Sample Search Results  

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

combustion are nitric oxide (NO) and nitrogen... of the nitric oxide is oxidized to nitrogen dioxide, so the environmental effects of emissions of both... O emissions at coal...

178

E-Print Network 3.0 - amperometric nitric oxide Sample Search...  

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

behavioral... Ref. Neurotransmitters and related compounds Nitric oxide (nitrite) Carbon fiber End-channelInt 8... been studied by microchip CEEC is nitric oxide (NO). NO...

179

Fluorescence-based detection methodologies for nitric oxide using transition metal scaffolds  

E-Print Network [OSTI]

Chapter 1. Fluorescence-Based Detection Methodologies for Nitric Oxide: A Review. Chapter 2. Cobalt Chemistry with Mixed Aminotroponimine Salicylaldimine Ligands: Synthesis, Characterization, and Nitric Oxide Reactivity. ...

Hilderbrand, Scott A. (Scott Alan), 1976-

2004-01-01T23:59:59.000Z

180

System for recovery of daughter isotopes from a source material  

DOE Patents [OSTI]

A method of separating isotopes from a mixture containing at least two isotopes in a solution is disclosed. A first isotope is precipitated and is collected from the solution. A daughter isotope is generated and collected from the first isotope. The invention includes a method of producing an actinium-225/bismuth-213 product from a material containing thorium-229 and thorium-232. A solution is formed containing nitric acid and the material containing thorium-229 and thorium-232, and iodate is added to form a thorium iodate precipitate. A supernatant is separated from the thorium iodate precipitate and a second volume of nitric acid is added to the thorium iodate precipitate. The thorium iodate precipitate is stored and a decay product comprising actinium-225 and bismuth-213 is generated in the second volume of nitric acid, which is then separated from the thorium iodate precipitate, filtered, and treated using at least one chromatographic procedure. A system for producing an actinium-225/bismuth-213 product is also disclosed.

Tranter, Troy J. (Idaho Falls, ID) [Idaho Falls, ID; Todd, Terry A. (Aberdeen, ID) [Aberdeen, ID; Lewis, Leroy C. (Idaho Falls, ID) [Idaho Falls, ID; Henscheid, Joseph P. (Idaho Falls, ID) [Idaho Falls, ID

2009-08-04T23:59:59.000Z

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


181

Effects of Acid Additives on Spent Acid Flowback through Carbonate Cores  

E-Print Network [OSTI]

Limestone and the non-emulsifying agent M-NEA the worst for Texas Cream Chalk for spent acid recovery after gas flowback....

Nasir, Ehsaan Ahmad

2012-07-16T23:59:59.000Z

182

E-Print Network 3.0 - acid molecules interacting Sample Search...  

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

of the TBP and Water on the Complexation of Uranyl Nitrate and the Dissolution of Nitric Acid into Supercritical CO2. A Theoretical Study Summary: molecules are involved in...

183

E-Print Network 3.0 - acid resistance test Sample Search Results  

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

> >> 1 JOURNAL OF MATERIALS SCIENCE 32 (1997) 1711--1715 Carbon blackhigh density polyethylene conducting Summary: treated with nitric acid for reaction times of 3, 12 and 24 h....

184

E-Print Network 3.0 - acid based black Sample Search Results  

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

> >> 1 JOURNAL OF MATERIALS SCIENCE 32 (1997) 1711--1715 Carbon blackhigh density polyethylene conducting Summary: surface. 2.2. Nitric acid treatment 200 g of the high structure...

185

Resource recovery - a byproduct of hazardous waste incineration  

SciTech Connect (OSTI)

Three principal areas of a chlorinated hydrocarbon waste disposal system for a typical vinyl chloride monomer (VCM) facility are described: the incinerator, the energy-recovery system, and the byproduct-recovery system. The overall efficiency of the energy- and *byproduct-recovery systems is dependent on the optimization of the primary combustor. An example is presented in table form which lists typical waste quantities for the plant and operating costs, including utility requirements for the incinerator system, the quench, absorber and scrubber. Savings that can result by the addition of the energy- and acid-recovery systems can pay for the waste disposal system and return money to the plant.

Santoleri, J.J.

1982-11-01T23:59:59.000Z

186

Waste Heat Recovery  

Office of Environmental Management (EM)

DRAFT - PRE-DECISIONAL - DRAFT 1 Waste Heat Recovery 1 Technology Assessment 2 Contents 3 1. Introduction to the TechnologySystem ......

187

Recovery Act Project Stories  

Broader source: Energy.gov [DOE]

Funded by the American Recovery and Reinvestment Act, these Federal Energy Management Program (FEMP) projects exemplify the range of technical assistance provided to federal agencies.

188

E-Print Network 3.0 - acetic acid cyano- Sample Search Results  

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

using Aliphatic Tertiary Amines. Summary: CHAPTER 6 Acetic Acid Recovery from Fast Pyrolysis oil. An Exploratory Study on Liquid... of large amounts of organic acids (acetic...

189

E-Print Network 3.0 - acid derivatives sorbtsionnye Sample Search...  

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

Aliphatic Tertiary Amines. Summary: , 6 due to increased demands for derivatives like vinyl acetate monomer (VAM). Currently, acetic acid... CHAPTER 6 Acetic Acid Recovery from...

190

E-Print Network 3.0 - anacardic acid derivatives Sample Search...  

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

Aliphatic Tertiary Amines. Summary: , 6 due to increased demands for derivatives like vinyl acetate monomer (VAM). Currently, acetic acid... CHAPTER 6 Acetic Acid Recovery from...

191

E-Print Network 3.0 - acid derivative hs-1200-induced Sample...  

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

Aliphatic Tertiary Amines. Summary: , 6 due to increased demands for derivatives like vinyl acetate monomer (VAM). Currently, acetic acid... CHAPTER 6 Acetic Acid Recovery from...

192

Recovery of phosphates from elemental phosphorus bearing wastes  

SciTech Connect (OSTI)

A process for oxidizing aqueous elemental phosphorus containing residues (sludges) to produce orthophosphate containing slurries suitable for subsequent reaction with ammonia to produce nitrogen and phosphate containing fertilizer products is presented. It comprises reacting aqueous elemental phosphorus containing residues with certain special mixtures of concentrated nitric acid and sulfuric acid to effect the conversion of the elemental phosphorus into mostly orthophosphoric acid and very little orthophosphorus acid with the relative ratios of the two acids being dependent upon the mole ratio of H{sub 2}SO{sub 4}:HNO{sub 3} employed in the processing. The resulting aqueous reaction intermediate is neutralized with ammonia during processing to a fluid or solid fertilizer product. Prior to the conversion to products, the aqueous reaction intermediate may be subjected to a solids separation step to remove insoluble salts of certain environmentally undesirable metals, such as Pb, Cd, Ba, and Cr.

Edwards, R.E.; Moore, O.E.; Sullivan, J.M.

1994-10-01T23:59:59.000Z

193

Recovery of Carboxylic Acids from Fermentation Broth via Acid Springing  

E-Print Network [OSTI]

. With government support, U.S. ethanol production increased about 25% from 3.9 billion gallons in 2005 (Form EIA-819, 2005) to 4.9 billion gallons in 2006 (Form EIA- 819, 2006). Meanwhile, the Renewable Fuels Association reported that the number of ethanol plants... operating in the United States increased from 95 in January of 2006 to 110 in January 2007, with 76 plants under construction or expansion (RFA website, 2008). In 2006, ethanol only accounted for about 4% of U.S. finished motor gasoline (EIA, 2007...

Dong, Jipeng

2010-01-14T23:59:59.000Z

194

Small Business Administration Recovery Act Implementation | Department...  

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

Small Business Administration Recovery Act Implementation Small Business Administration Recovery Act Implementation Small Business Administration Recovery Act Implementation Small...

195

Recovery Boiler Corrosion Chemistry  

E-Print Network [OSTI]

11/13/2014 1 Recovery Boiler Corrosion Chemistry Sandy Sharp and Honghi Tran Symposium on Corrosion of a recovery boiler each cause their own forms of corrosion and cracking Understanding the origin of the corrosive conditions enables us to operate a boiler so as to minimize corrosion and cracking select

Das, Suman

196

Mass and Heat Recovery  

E-Print Network [OSTI]

In the last few years heat recovery was under spot and in air conditioning fields usually we use heat recovery by different types of heat exchangers. The heat exchanging between the exhaust air from the building with the fresh air to the building...

Hindawai, S. M.

2010-01-01T23:59:59.000Z

197

Jobs Creation Economic Recovery  

E-Print Network [OSTI]

Commission (Energy Commission) collects the American Recovery and Reinvestment Act of 2009 (ARRA) jobs creation and retention data (jobs data) from its subrecipients through the Energy Commission's ARRAJobs Creation and Economic Recovery Prompt, Fair, and Reasonable Use of ARRA Funds Subrecipient

198

Recovery Act Funds at Work  

Broader source: Energy.gov [DOE]

Funds from the American Recovery and Reinvestment Act of 2009 (Recovery Act) are being put to work to improve safety, reliability, and service in systems across the country. Here are case studies from a variety of Recovery Act programs.

199

Hydrogen peroxide differentially modulates cardiac myocyte nitric oxide synthesis  

E-Print Network [OSTI]

Nitric oxide (NO) and hydrogen peroxide (H(subscript 2)O(subscript 2)) are synthesized within cardiac myocytes and play key roles in modulating cardiovascular signaling. Cardiac myocytes contain both the endothelial (eNOS) ...

Sartoretto, Juliano

200

Distribution of 1-butanol between organic solvent and acidic solution  

SciTech Connect (OSTI)

1-butanol, a major TBP-degraded product, is known to react explosively with concentrated nitric acid under non-heated conditions. However, no quantitative data is available on the distribution behavior in the Purex solution. The distribution of 1-butanol between tributyl phosphate(TBP) diluted with n-dodecane and aqueous solution of nitric acid and uranyl nitrate was investigated under various conditions, by changing the concentration of nitric acid, uranyl nitrate, the composition of the organic mixture, the organic to aqueous phase volume ratio, and temperature. 1-butanol was found to distribute more in solvent phase, but the distribution ratio is not large, less than four under typical Purex solution conditions. The ratio was found to be correlated with the molar concentration of free TBP and 1-butanol. Effects of these characteristics on safety in radiochemical plants will be discussed from the local accumulation of 1-butanol.

Asakura, T.; Nemoto, H.; Uchiyama, G. [Japan Atomic Energy Research Institute, Ibaraki-ken (Japan)] [and others

1995-12-01T23:59:59.000Z

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


201

Solvent recycle/recovery  

SciTech Connect (OSTI)

This report describes Phase I of the Solvent Recycle/Recovery Task of the DOE Chlorinated Solvent Substitution Program for the US Air Force by the Idaho National Engineering Laboratory, EG G Idaho, Inc., through the US Department of Energy, Idaho Operations Office. The purpose of the task is to identify and test recovery and recycling technologies for proposed substitution solvents identified by the Biodegradable Solvent Substitution Program and the Alternative Solvents/Technologies for Paint Stripping Program with the overall objective of minimizing hazardous wastes. A literature search to identify recycle/recovery technologies and initial distillation studies has been conducted. 4 refs.

Paffhausen, M.W.; Smith, D.L.; Ugaki, S.N.

1990-09-01T23:59:59.000Z

202

Imbibition assisted oil recovery  

E-Print Network [OSTI]

analyzed in detail to investigate oil recovery during spontaneous imbibition with different types of boundary conditions. The results of these studies have been upscaled to the field dimensions. The validity of the new definition of characteristic length...

Pashayev, Orkhan H.

2004-11-15T23:59:59.000Z

203

A high frequency titration of indium with benzenephosphinic acid  

E-Print Network [OSTI]

with ordinary oxidizing agents as hydrogen peroxide and nitric acid. (31) Michaells and Ananoff first reported the preparation and properties of benzenepbosphinic acid in 1874 (25). Kichaells prepared the potassium, barium, calcium, and iron salts... in approximately 25 milliliters of the acid These solutions were heated on a hot plate until dry. The salt was dissolved in dis- tilled water, and diluted to one liter in a volumetric flask. These solutions were standardised volumetrically with EDTA (13...

Keilt, Francis Xavier

1960-01-01T23:59:59.000Z

204

Recovery of Water from Boiler Flue Gas  

SciTech Connect (OSTI)

This project dealt with use of condensing heat exchangers to recover water vapor from flue gas at coal-fired power plants. Pilot-scale heat transfer tests were performed to determine the relationship between flue gas moisture concentration, heat exchanger design and operating conditions, and water vapor condensation rate. The tests also determined the extent to which the condensation processes for water and acid vapors in flue gas can be made to occur separately in different heat transfer sections. The results showed flue gas water vapor condensed in the low temperature region of the heat exchanger system, with water capture efficiencies depending strongly on flue gas moisture content, cooling water inlet temperature, heat exchanger design and flue gas and cooling water flow rates. Sulfuric acid vapor condensed in both the high temperature and low temperature regions of the heat transfer apparatus, while hydrochloric and nitric acid vapors condensed with the water vapor in the low temperature region. Measurements made of flue gas mercury concentrations upstream and downstream of the heat exchangers showed a significant reduction in flue gas mercury concentration within the heat exchangers. A theoretical heat and mass transfer model was developed for predicting rates of heat transfer and water vapor condensation and comparisons were made with pilot scale measurements. Analyses were also carried out to estimate how much flue gas moisture it would be practical to recover from boiler flue gas and the magnitude of the heat rate improvements which could be made by recovering sensible and latent heat from flue gas.

Edward Levy; Harun Bilirgen; Kwangkook Jeong; Michael Kessen; Christopher Samuelson; Christopher Whitcombe

2008-09-30T23:59:59.000Z

205

Recovery of fissile materials from nuclear wastes  

DOE Patents [OSTI]

A process for recovering fissile materials such as uranium, and plutonium, and rare earth elements, from complex waste feed material, and converting the remaining wastes into a waste glass suitable for storage or disposal. The waste feed is mixed with a dissolution glass formed of lead oxide and boron oxide resulting in oxidation, dehalogenation, and dissolution of metal oxides. Carbon is added to remove lead oxide, and a boron oxide fusion melt is produced. The fusion melt is essentially devoid of organic materials and halogens, and is easily and rapidly dissolved in nitric acid. After dissolution, uranium, plutonium and rare earth elements are separated from the acid and recovered by processes such as PUREX or ion exchange. The remaining acid waste stream is vitrified to produce a waste glass suitable for storage or disposal. Potential waste feed materials include plutonium scrap and residue, miscellaneous spent nuclear fuel, and uranium fissile wastes. The initial feed materials may contain mixtures of metals, ceramics, amorphous solids, halides, organic material and other carbon-containing material.

Forsberg, Charles W. (Oak Ridge, TN)

1999-01-01T23:59:59.000Z

206

Development and testing of an advanced acid fracture conductivity apparatus  

E-Print Network [OSTI]

wells. Acid fracturing is a standard practice to increase the production rate and to improve ultimate recovery in carbonate reservoirs. There have been successful cases in most carbonate reservoirs around the world. However acid fracture performance...

Zou, ChunLei

2006-08-16T23:59:59.000Z

207

Thermal Recovery Methods  

SciTech Connect (OSTI)

Thermal Recovery Methods describes the basic concepts of thermal recovery and explains the injection patterns used to exploit reservoir conditions. Basic reservoir engineering is reviewed with an emphasis on changes in flow characteristics caused by temperature. The authors discuss an energy balance for steam and combustion drive, and they explain in situ reactions. Heat loss, combustion drive, and steam displacement also are examined in detail, as well as cyclic steam injection, downhole ignition, well heating, and low-temperature oxidation. Contents: Thermal processes; Formation and reservoir evaluations; Well patterns and spacing; Flow and process equations; Laboratory simulation of thermal recovery; Heat loss and transmission; Displacement and production; Equipment; Basic data for field selection; Laboratory evaluation of combustion characteristics; Thermal properties of reservoirs and fluids.

White, P.D.; Moss, J.T.

1983-01-01T23:59:59.000Z

208

Enhanced coalbed methane recovery  

SciTech Connect (OSTI)

The recovery of coalbed methane can be enhanced by injecting CO{sub 2} in the coal seam at supercritical conditions. Through an in situ adsorption/desorption process the displaced methane is produced and the adsorbed CO{sub 2} is permanently stored. This is called enhanced coalbed methane recovery (ECBM) and it is a technique under investigation as a possible approach to the geological storage of CO{sub 2} in a carbon dioxide capture and storage system. This work reviews the state of the art on fundamental and practical aspects of the technology and summarizes the results of ECBM field tests. These prove the feasibility of ECBM recovery and highlight substantial opportunities for interdisciplinary research at the interface between earth sciences and chemical engineering.

Mazzotti, M.; Pini, R.; Storti, G. [ETH, Zurich (Switzerland). Inst. of Process Engineering

2009-01-15T23:59:59.000Z

209

Method for the recovery of uranium values from uranium tetrafluoride  

DOE Patents [OSTI]

The invention is a novel method for the recovery of uranium from dry, particulate uranium tetrafluoride. In one aspect, the invention comprises reacting particulate uranium tetrafluoride and calcium oxide in the presence of gaseous oxygen to effect formation of the corresponding alkaline earth metal uranate and alkaline earth metal fluoride. The product uranate is highly soluble in various acidic solutions wherein the product fluoride is virtually insoluble therein. The product mixture of uranate and alkaline earth metal fluoride is contacted with a suitable acid to provide a uranium-containing solution, from which the uranium is recovered. The invention can achieve quantitative recovery of uranium in highly pure form.

Kreuzmann, Alvin B. (Cincinnati, OH)

1983-01-01T23:59:59.000Z

210

Method for the recovery of uranium values from uranium tetrafluoride  

DOE Patents [OSTI]

The invention is a novel method for the recovery of uranium from dry, particulate uranium tetrafluoride. In one aspect, the invention comprises reacting particulate uranium tetrafluoride and calcium oxide in the presence of gaseous oxygen to effect formation of the corresponding alkaline earth metal uranate and alkaline earth metal fluoride. The product uranate is highly soluble in various acidic solutions whereas the product fluoride is virtually insoluble therein. The product mixture of uranate and alkaline earth metal fluoride is contacted with a suitable acid to provide a uranium-containing solution, from which the uranium is recovered. The invention can achieve quantitative recovery of uranium in highly pure form.

Kreuzmann, A.B.

1982-10-27T23:59:59.000Z

211

Metal-based turn-on fluorescent probes for nitric oxide sensing  

E-Print Network [OSTI]

Chapter 1. Metal-Based Turn-On Fluorescent Probes for Sensing Nitric Oxide. Nitric oxide, a reactive free radical, regulates a variety of biological processes. The absence of tools to detect NO directly, rapidly, specifically ...

Lim, Mi Hee

2006-01-01T23:59:59.000Z

212

Nitric Oxide in Astrocyte-Neuron Signaling  

SciTech Connect (OSTI)

Astrocytes, a subtype of glial cell, have recently been shown to exhibit Ca{sup 2+} elevations in response to neurotransmitters. A Ca{sup 2+} elevation can propagate to adjacent astrocytes as a Ca{sup 2+} wave, which allows an astrocyte to communicate with its neighbors. Additionally, glutamate can be released from astrocytes via a Ca{sup 2+}-dependent mechanism, thus modulating neuronal activity and synaptic transmission. In this dissertation, the author investigated the roles of another endogenous signal, nitric oxide (NO), in astrocyte-neuron signaling. First the author tested if NO is generated during astrocytic Ca{sup 2+} signaling by imaging NO in purified murine cortical astrocyte cultures. Physiological concentrations of a natural messenger, ATP, caused a Ca{sup 2+}-dependent NO production. To test the roles of NO in astrocytic Ca{sup 2+} signaling, the author applied NO to astrocyte cultures via addition of a NO donor, S-nitrosol-N-acetylpenicillamine (SNAP). NO induced an influx of external Ca{sup 2+}, possibly through store-operated Ca{sup 2+} channels. The NO-induced Ca{sup 2+} signaling is cGMP-independent since 8-Br-cGMP, an agonistic analog of cGMP, did not induce a detectable Ca{sup 2+} change. The consequence of this NO-induced Ca{sup 2+} influx was assessed by simultaneously monitoring of cytosolic and internal store Ca{sup 2+} using fluorescent Ca{sup 2+} indicators x-rhod-1 and mag-fluo-4. Blockage of NO signaling with the NO scavenger PTIO significantly reduced the refilling percentage of internal stores following ATP-induced Ca{sup 2+} release, suggesting that NO modulates internal store refilling. Furthermore, locally photo-release of NO to a single astrocyte led to a Ca{sup 2+} elevation in the stimulated astrocyte and a subsequent Ca{sup 2+} wave to neighbors. Finally, the author tested the role of NO inglutamate-mediated astrocyte-neuron signaling by recording the astrocyte-evoked glutamate-dependent neuronal slow inward current (SIC). Although NO is not required for the SIC,PTIO reduced SIC amplitude, suggesting that NO modulates glutamate release from astrocytes or glutamate receptor sensitivity of neurons.

Nianzhen Li

2002-06-27T23:59:59.000Z

213

Development of Acetic Acid Removal Technology for the UREX+Process  

SciTech Connect (OSTI)

It is imperative that acetic acid is removed from a waste stream in the UREX+process so that nitric acid can be recycled and possible interference with downstreatm steps can be avoidec. Acetic acid arises from acetohydrozamic acid (AHA), and is used to suppress plutonium in the first step of the UREX+process. Later, it is hydrolyzed into hydroxyl amine nitrate and acetic acid. Many common separation technologies were examined, and solvent extraction was determined to be the best choice under process conditions. Solvents already used in the UREX+ process were then tested to determine if they would be sufficient for the removal of acetic acid. The tributyl phosphage (TBP)-dodecane diluent, used in both UREX and NPEX, was determined to be a solvent system that gave sufficient distribution coefficients for acetic acid in addition to a high separation factor from nitric acid.

Robert M. Counce; Jack S. Watson

2009-06-30T23:59:59.000Z

214

Recovery Act Recipient Data | Department of Energy  

Office of Environmental Management (EM)

Recovery Act Recipient Data Recovery Act Recipient Data A listing of all Recovery Act recipients and their allocations. Updated weekly. recoveryactfunding.xls More Documents &...

215

Some Thoughts on Econometric Information Recovery  

E-Print Network [OSTI]

Paper 1135 Some Thoughts on Econometric Information Recoverys). Some Thoughts on Econometric Information Recovery GeorgeTheoretic Approach To Econometric Information Recovery

Judge, George G.

2013-01-01T23:59:59.000Z

216

Challenges in Industrial Heat Recovery  

E-Print Network [OSTI]

This presentation will address several completed and working projects involving waste heat recovery in a chemical plant. Specific examples will be shown and some of the challenges to successful implementation and operation of heat recovery projects...

Dafft, T.

2007-01-01T23:59:59.000Z

217

Can You Afford Heat Recovery?  

E-Print Network [OSTI]

many companies to venture into heat recovery projects without due consideration of the many factors involved. Many of these efforts have rendered less desirable results than expected. Heat recovery in the form of recuperation should be considered...

Foust, L. T.

1983-01-01T23:59:59.000Z

218

[Waste water heat recovery system  

SciTech Connect (OSTI)

The production capabilities for and field testing of the heat recovery system are described briefly. Drawings are included.

Not Available

1993-04-28T23:59:59.000Z

219

Measurement of nitric oxide with an antimonide diode laser  

E-Print Network [OSTI]

lasers while retaining the practical advantages of room- temperature or thermoelectrically cooled the selective detection of NO under reduced pressure conditions was identified. With wavelength- modulation cooling is not required. © 1997 Optical Society of America Key words: Diode laser, antimonide, nitric

220

Magnesium fluoride recovery method  

DOE Patents [OSTI]

A method of obtaining magnesium fluoride substantially free from radioactive uranium from a slag containing the same and having a radioactivity level of at least about 7000 pCi/gm. The slag is ground to a particle size of about 200 microns or less. The ground slag is contacted with an acid under certain prescribed conditions to produce a liquid product and a particulate solid product. The particulate solid product is separated from the liquid and treated at least two more times with acid to produce a solid residue consisting essentially of magnesium fluoride substantially free of uranium and having a residual radioactivity level of less than about 1000 pCi/gm. In accordance with a particularly preferred embodiment of the invention a catalyst and an oxidizing agent are used during the acid treatment and preferably the acid is sulfuric acid having a strength of about 1.0 Normal.

Gay, Richard L. (Canoga Park, CA); McKenzie, Donald E. (Woodland Hills, CA)

1989-01-01T23:59:59.000Z

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


221

Elemental sulfur recovery process  

DOE Patents [OSTI]

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

Flytzani-Stephanopoulos, M.; Zhicheng Hu.

1993-09-07T23:59:59.000Z

222

Recovery Boiler Modeling  

E-Print Network [OSTI]

, east, e, west, w, bot tom, b, and top, t, neighbors. The neighboring cou pling coefficients (an, a., .. , etc) express the magnitudes of the convection and diffusion which occur across the control volume boundaries. The variable b p represents... represents a model of one half of the recovery boiler. The boiler has three air levels. The North, South and East boundaries of the computational domain represent the water walls of the boiler. The West boundary represents a symmetry plane. It should...

Abdullah, Z.; Salcudean, M.; Nowak, P.

223

Process for tertiary oil recovery using tall oil pitch  

DOE Patents [OSTI]

A process and compositions for enhancing the recovery of acid crudes are disclosed. The process involves injecting caustic solutions into the reservoir to maintain a pH of 11 to 13. The fluid contains an effective amount of multivalent cation for inhibiting alkaline silica dissolution with the reservoir. A tall oil pitch soap is added as a polymeric mobility control agent. (DMC)

Radke, C.J.

1983-07-25T23:59:59.000Z

224

Waste Heat Recovery Opportunities for Thermoelectric Generators...  

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

Waste Heat Recovery Opportunities for Thermoelectric Generators Waste Heat Recovery Opportunities for Thermoelectric Generators Thermoelectrics have unique advantages for...

225

Enhanced Oil Recovery: Aqueous Flow Tracer Measurement  

SciTech Connect (OSTI)

A low detection limit analytical method was developed to measure a suite of benzoic acid and fluorinated benzoic acid compounds intended for use as tracers for enhanced oil recovery operations. Although the new high performance liquid chromatography separation successfully measured the tracers in an aqueous matrix at low part per billion levels, the low detection limits could not be achieved in oil field water due to interference problems with the hydrocarbon-saturated water using the system's UV detector. Commercial instrument vendors were contacted in an effort to determine if mass spectrometry could be used as an alternate detection technique. The results of their work demonstrate that low part per billion analysis of the tracer compounds in oil field water could be achieved using ultra performance liquid chromatography mass spectrometry.

Joseph Rovani; John Schabron

2009-02-01T23:59:59.000Z

226

ARM - Recovery Act  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary)morphinanInformation InInformation InExplosionAnnouncementsgovMeasurementsgovPublicationsPublicgovAboutRecovery

227

ARM - Recovery Act Instruments  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc Documentation RUC :ProductsSCM Forcing Data DerivedInstruments Related Links RelatedActRecovery

228

Recovery Act | Department of Energy  

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

three Recovery Act-funded Smart Grid Investment Grant (SGIG) projects. February 28, 2014 Smart Meter Investments Yield Positive Results in Maine Central Maine Power's (CMP) SGIG...

229

Economic Recovery Loan Program (Maine)  

Broader source: Energy.gov [DOE]

The Economic Recovery Loan Program provides subordinate financing to help businesses remain viable and improve productivity. Eligibility criteria are based on ability to repay, and the loan is...

230

E-Print Network 3.0 - ascorbic acid protects Sample Search Results  

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

recovery... cord white mat- ter, similar protection of ascorbic acid against acrolein- induced damage... Original Paper Pathobiology 2005;72:171-178 DOI: 10.1159000086786...

231

Asthmatic responses to airborne acid aerosols  

SciTech Connect (OSTI)

Controlled exposure studies suggest that asthmatics may be more sensitive to the respiratory effects of acidic aerosols than individuals without asthma. This study investigates whether acidic aerosols and other air pollutants are associated with respiratory symptoms in free-living asthmatics. Daily concentrations of hydrogen ion (H+), nitric acid, fine particulates, sulfates and nitrates were obtained during an intensive air monitoring effort in Denver, Colorado, in the winter of 1987-88. A panel of 207 asthmatics recorded respiratory symptoms, frequency of medication use, and related information in daily diaries. We used a multiple regression time-series model to analyze which air pollutants, if any, were associated with health outcomes reported by study participants. Airborne H+ was found to be significantly associated with several indicators of asthma status, including moderate or severe cough and shortness of breath. Cough was also associated with fine particulates, and shortness of breath with sulfates. Incorporating the participants' time spent outside and exercise intensity into the daily measure of exposure strengthened the association between these pollutants and asthmatic symptoms. Nitric acid and nitrates were not significantly associated with any respiratory symptom analyzed. In this population of asthmatics, several outdoor air pollutants, particularly airborne acidity, were associated with daily respiratory symptoms.

Ostro, B.D.; Lipsett, M.J.; Wiener, M.B.; Selner, J.C. (California Department of Health Services, Berkeley (USA))

1991-06-01T23:59:59.000Z

232

Oxidation of trace amounts of transplutonium elements to the tetravalent state in solutions of mineral acids and their stabilities  

SciTech Connect (OSTI)

The behavior of trace amounts of americium(IV) in sulfuric and nitric acid solutions as a function of the mineral acid, potassium phosphotungstate, and ammonium persulfate concentrations was investigated. The stability of americium(IV) was studied. The optimal conditions and time of oxidation of trace amounts of americium to the tetravalent state were found on the basis of the experimental data obtained.

Milyukova, M.S.; Varezhkina, N.S.; Kuzovkina, E.V.; Malikov, D.A.; Myasoedov, B.F.

1989-01-01T23:59:59.000Z

233

Actinide recovery process  

DOE Patents [OSTI]

Process for the removal of plutonium polymer and ionic actinides from aqueous solutions by absorption onto a solid extractant loaded on a solid inert support such as polystyrenedivinylbenzene. The absorbed actinides can then be recovered by incineration, by stripping with organic solvents, or by acid digestion. Preferred solid extractants are trioctylphosphine oxide and octylphenyl-N,N-diisobutylcarbamoylmethylphosphine oxide and the like.

Muscatello, Anthony C. (Arvada, CO); Navratil, James D. (Arvada, CO); Saba, Mark T. (Arvada, CO)

1987-07-28T23:59:59.000Z

234

Energy recovery system  

DOE Patents [OSTI]

The present invention is directed to an improved wet air oxidation system and method for reducing the chemical oxygen demand (COD) of waste water used from scrubbers of coal gasification plants, with this COD reduction being sufficient to effectively eliminate waste water as an environmental pollutant. The improvement of the present invention is provided by heating the air used in the oxidation process to a temperature substantially equal to the temperature in the oxidation reactor before compressing or pressurizing the air. The compression of the already hot air further heats the air which is then passed in heat exchange with gaseous products of the oxidation reaction for "superheating" the gaseous products prior to the use thereof in turbines as the driving fluid. The superheating of the gaseous products significantly minimizes condensation of gaseous products in the turbine so as to provide a substantially greater recovery of mechanical energy from the process than heretofore achieved.

Moore, Albert S. (Morgantown, WV); Verhoff, Francis H. (Morgantown, WV)

1980-01-01T23:59:59.000Z

235

Enhanced oil recovery system  

DOE Patents [OSTI]

All energy resources available from a geopressured geothermal reservoir are used for the production of pipeline quality gas using a high pressure separator/heat exchanger and a membrane separator, and recovering waste gas from both the membrane separator and a low pressure separator in tandem with the high pressure separator for use in enhanced oil recovery, or in powering a gas engine and turbine set. Liquid hydrocarbons are skimmed off the top of geothermal brine in the low pressure separator. High pressure brine from the geothermal well is used to drive a turbine/generator set before recovering waste gas in the first separator. Another turbine/generator set is provided in a supercritical binary power plant that uses propane as a working fluid in a closed cycle, and uses exhaust heat from the combustion engine and geothermal energy of the brine in the separator/heat exchanger to heat the propane.

Goldsberry, Fred L. (Spring, TX)

1989-01-01T23:59:59.000Z

236

Hydraulic waste energy recovery  

SciTech Connect (OSTI)

Water distribution systems are typically a municipality's largest consumer of energy and greatest expense. The water distribution network has varying pressure requirements due to the age of the pipeline and topographical differences. Certain circumstances require installation of pressure reducing devices in the pipeline to lower the water pressure in the system. The consequence of this action is that the hydraulic energy supplied by the high lift or booster pumps is wasted in the process of reducing the pressure. A possible solution to capture the waste hydraulic energy is to install an in-line electricity generating turbine. Energy recovery using in-line turbine systems is an emerging technology. Due to the lack of technical and other relevant information on in-line turbine system installations, questions of constructability and legal issues over the power service contract have yet to be answered. This study seeks to resolve these questions and document the findings so that other communities may utilize this information. 10 figs.

Lederer, C.C.; Thomas, A.H.; McGuire, J.L. (Detroit Buildings and Safety Engineering Dept., MI (USA))

1990-12-01T23:59:59.000Z

237

Speech recovery device  

DOE Patents [OSTI]

There is provided an apparatus and method for assisting speech recovery in people with inability to speak due to aphasia, apraxia or another condition with similar effect. A hollow, rigid, thin-walled tube with semi-circular or semi-elliptical cut out shapes at each open end is positioned such that one end mates with the throat/voice box area of the neck of the assistor and the other end mates with the throat/voice box area of the assisted. The speaking person (assistor) makes sounds that produce standing wave vibrations at the same frequency in the vocal cords of the assisted person. Driving the assisted person's vocal cords with the assisted person being able to hear the correct tone enables the assisted person to speak by simply amplifying the vibration of membranes in their throat.

Frankle, Christen M.

2004-04-20T23:59:59.000Z

238

Personal and Ambient Air Pollution is Associated with Increased Exhaled Nitric Oxide in Children with Asthma  

E-Print Network [OSTI]

1994. Nitric oxide and nitrogen dioxide: Method 6014. In:Molecular mechanisms of nitrogen dioxide induced epithelialEC, OC), and 24-hr nitrogen dioxide. Ambient exposures

2006-01-01T23:59:59.000Z

239

Metal recovery from porous materials  

DOE Patents [OSTI]

The present invention relates to recovery of metals. More specifically, the present invention relates to the recovery of plutonium and other metals from porous materials using microwaves. The United States Government has rights in this invention pursuant to Contract No. DE-AC09-89SR18035 between the US Department of Energy and Westinghouse Savannah River Company.

Sturcken, E.F.

1991-01-01T23:59:59.000Z

240

Electrochemical catalyst recovery method  

DOE Patents [OSTI]

A method of recovering catalyst material from latent catalyst material solids includes: (a) combining latent catalyst material solids with a liquid acid anolyte solution and a redox material which is soluble in the acid anolyte solution to form a mixture; (b) electrochemically oxidizing the redox material within the mixture into a dissolved oxidant, the oxidant having a potential for oxidation which is effectively higher than that of the latent catalyst material; (c) reacting the oxidant with the latent catalyst material to oxidize the latent catalyst material into at least one oxidized catalyst species which is soluble within the mixture and to reduce the oxidant back into dissolved redox material; and (d) recovering catalyst material from the oxidized catalyst species of the mixture. The invention is expected to be particularly useful in recovering spent catalyst material from petroleum hydroprocessing reaction waste products having adhered sulfides, carbon, hydrocarbons, and undesired metals, and as well as in other industrial applications. 3 figs.

Silva, L.J.; Bray, L.A.

1995-05-30T23:59:59.000Z

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


241

Actinide recovery process  

DOE Patents [OSTI]

Process for the removal of plutonium polymer and ionic actinides from aqueous solutions by absorption onto a solid extractant loaded on a solid inert support such as polystyrene-divinylbenzene. The absorbed actinides can then be recovered by incineration, by stripping with organic solvents, or by acid digestion. Preferred solid extractants are trioctylphosphine oxide and octylphenyl-N,N-diisobutylcarbamoylmethylphosphine oxide and the like. 2 tabs.

Muscatello, A.C.; Navratil, J.D.; Saba, M.T.

1985-06-13T23:59:59.000Z

242

Recovery Act Milestones | Department of Energy  

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

Recovery and Reinvestment Act. Update at 200 days, hosted by Matt Rogers, Senior Advisor to Secretary Steven Chu for Recovery Act Implementation. Speakers Matt Rogers...

243

Recovery Act?Transportation Electrification Education Partnership...  

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

Recovery ActTransportation Electrification Education Partnership for Green Jobs and Sustainable Mobility Recovery ActTransportation Electrification Education Partnership for...

244

Optimize carbon dioxide sequestration, enhance oil recovery  

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

Optimize carbon dioxide sequestration, enhance oil recovery Optimize carbon dioxide sequestration, enhance oil recovery The simulation provides an important approach to estimate...

245

Bonneville Power Administration Program Specific Recovery Plan...  

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

Bonneville Power Administration Program Specific Recovery Plan Bonneville Power Administration Program Specific Recovery Plan Microsoft Word - PSRP May 15 2009 BPA Final.docx...

246

Wastewater heat recovery apparatus  

DOE Patents [OSTI]

A heat recovery system is described with a heat exchanger and a mixing valve. A drain trap includes a heat exchanger with an inner coiled tube, baffle plate, wastewater inlet, wastewater outlet, cold water inlet, and preheated water outlet. Wastewater enters the drain trap through the wastewater inlet, is slowed and spread by the baffle plate, and passes downward to the wastewater outlet. Cold water enters the inner tube through the cold water inlet and flows generally upward, taking on heat from the wastewater. This preheated water is fed to the mixing valve, which includes a flexible yoke to which are attached an adjustable steel rod, two stationary zinc rods, and a pivoting arm. The free end of the arm forms a pad which rests against a valve seat. The rods and pivoting arm expand or contract as the temperature of the incoming preheated water changes. The zinc rods expand more than the steel rod, flexing the yoke and rotating the pivoting arm. The pad moves towards the valve seat as the temperature of the preheated water rises, and away as the temperature falls, admitting a variable amount of hot water to maintain a nearly constant average process water temperature. 6 figs.

Kronberg, J.W.

1992-09-01T23:59:59.000Z

247

Wastewater heat recovery apparatus  

DOE Patents [OSTI]

A heat recovery system with a heat exchanger and a mixing valve. A drain trap includes a heat exchanger with an inner coiled tube, baffle plate, wastewater inlet, wastewater outlet, cold water inlet, and preheated water outlet. Wastewater enters the drain trap through the wastewater inlet, is slowed and spread by the baffle plate, and passes downward to the wastewater outlet. Cold water enters the inner tube through the cold water inlet and flows generally upward, taking on heat from the wastewater. This preheated water is fed to the mixing valve, which includes a flexible yoke to which are attached an adjustable steel rod, two stationary zinc rods, and a pivoting arm. The free end of the arm forms a pad which rests against a valve seat. The rods and pivoting arm expand or contract as the temperature of the incoming preheated water changes. The zinc rods expand more than the steel rod, flexing the yoke and rotating the pivoting arm. The pad moves towards the valve seat as the temperature of the preheated water rises, and away as the temperature falls, admitting a variable amount of hot water to maintain a nearly constant average process water temperature.

Kronberg, James W. (108 Independent Blvd., Aiken, SC 29801)

1992-01-01T23:59:59.000Z

248

Mineral Nutrient Recovery from Pyrolysis Co-Products  

E-Print Network [OSTI]

. 2 For highly cellulosic biomass feedstocks (i.e. sorghum, switchgrass, ect.), the pyrolyzed liquid fraction usually contains acids, alcohols, aldehydes, ketones, esters, heterocyclic derivatives and phenolic compounds (Yaman, 2004). Bio... has revealed that most of these inorganic compounds, especially K, Ca, Na, Si, P, and Cl, are constituents of the ash in biomass feedstocks (Agblevor and Besler, 1996). High recoveries P and K were reported for bio-char derived from fluidized...

Wise, Jatara Rob

2012-07-16T23:59:59.000Z

249

Recovery of gallium from aluminum industry residues  

SciTech Connect (OSTI)

A procedure is proposed to recover gallium from flue dust aluminum residues produced in plants by using solid-phase extraction with a commercial polyether-type polyurethane foam (PUF). Gallium can be separated from high concentrations of aluminum, iron, nickel, titanium, vanadium, copper, zinc, sulfate, fluoride, and chloride by extraction with PUF from 3 M sulfuric acid and 3 M sodium chloride concentration medium with at least a 92% efficiency. Gallium backextraction was fast and quantitative with ethanol solution. In all recovery steps commercial-grade reagents could be used, including tap water. The recovered gallium was precipitated with sodium hydroxide solution, purified by dissolution and precipitation, calcinated, and the final oxide was 98.6% pure.

Carvalho, M.S.; Neto, K.C.M.; Nobrega, A.W.; Medeiros, J.A.

2000-01-01T23:59:59.000Z

250

Heat Recovery Steam Generator Simulation  

E-Print Network [OSTI]

The paper discusses the applications of Heat Recovery Steam Generator Simulation. Consultants, plant engineers and plant developers can evaluate the steam side performance of HRSGs and arrive at the optimum system which matches the needs...

Ganapathy, V.

251

Recovery Act Funding Opportunities Webcast  

Broader source: Energy.gov [DOE]

As a result of the 2009 American Reinvestment and Recovery Act, the Geothermal Technologies Office (GTO) has four open Funding Opportunity Announcements (FOAs) totaling $484 million for cost-shared...

252

Recovery and purification of ethylene  

SciTech Connect (OSTI)

A process for the recovery and purification of ethylene and optionally propylene from a stream containing lighter and heavier components that employs an ethylene distributor column and a partially thermally coupled distributed distillation system.

Reyneke, Rian (Katy, TX); Foral, Michael J. (Aurora, IL); Lee, Guang-Chung (Houston, TX); Eng, Wayne W. Y. (League City, TX); Sinclair, Iain (Warrington, GB); Lodgson, Jeffery S. (Naperville, IL)

2008-10-21T23:59:59.000Z

253

Olefin recovery via chemical absorption  

SciTech Connect (OSTI)

The recovery of fight olefins in petrochemical plants has generally been accomplished through cryogenic distillation, a process which is very capital and energy intensive. In an effort to simplify the recovery process and reduce its cost, BP Chemicals has developed a chemical absorption technology based on an aqueous silver nitrate solution. Stone & Webster is now marketing, licensing, and engineering the technology. The process is commercially ready for recovering olefins from olefin derivative plant vent gases, such as vents from polyethylene, polypropylene, ethylene oxide, and synthetic ethanol units. The process can also be used to debottleneck C{sub 2} or C{sub 3} splinters, or to improve olefin product purity. This paper presents the olefin recovery imp technology, discusses its applications, and presents economics for the recovery of ethylene and propylene.

Barchas, R. [Stone & Webster Engineering Corporation, Houston, TX (United States)

1998-06-01T23:59:59.000Z

254

Low Level Heat Recovery Technology  

E-Print Network [OSTI]

level heat recovery technology. This paper discusses heat distribution systems, latest developments in absorption refrigeration and organic Rankine cycles, and pressure, minimization possibilities. The relative merits and economics of the various...

O'Brien, W. J.

1982-01-01T23:59:59.000Z

255

Waste Heat Recovery from Refrigeration  

E-Print Network [OSTI]

heat recovery from refrigeration machines is a concept which has great potential for implementation in many businesses. If a parallel requirement for refrigeration and hot water exists, the installation of a system to provide hot water as a by...

Jackson, H. Z.

1982-01-01T23:59:59.000Z

256

The Effect of Rock Phosphate Upon the Corn Possibility of Phosphoric Acid of the Soil  

E-Print Network [OSTI]

of Veterinary Medicine, A. and M. College of Texas. **In cooperation with United Statee Department of Agriculture. THE EFFECT OF ROCK PHOSPHATE UPON THE CORN POS- SIBILITY OF PHOSPHORIC ACID OF THE SOIL. In connection vith oil-fertilit~ stuclies..., it is important to lcnow the relation between the effect of the phosphoric acid of the rock phosphate on crops and the phosphoric acid that can be withdrawn from the soil by crops. The phosphoric acid of rock phosphate is readily soluble in K/5 nitric acid...

Fraps, G. S. (George Stronach)

1922-01-01T23:59:59.000Z

257

Developing a Regional Recovery Framework  

SciTech Connect (OSTI)

Abstract A biological attack would present an unprecedented challenge for local, state, and federal agencies; the military; the private sector; and individuals on many fronts ranging from vaccination and treatment to prioritization of cleanup actions to waste disposal. To prepare the Seattle region to recover from a biological attack, the Seattle Urban Area Security Initiative (UASI) partners collaborated with military and federal agencies to develop a Regional Recovery Framework for a Biological Attack in the Seattle Urban Area. The goal was to reduce the time and resources required to recover and restore wide urban areas, military installations, and other critical infrastructure following a biological incident by providing a coordinated systems approach. Based on discussions in small workshops, tabletop exercises, and interviews with emergency response agency staff, the partners identified concepts of operation for various areas to address critical issues the region will face as recovery progresses. Key to this recovery is the recovery of the economy. Although the Framework is specific to a catastrophic, wide-area biological attack using anthrax, it was designed to be flexible and scalable so it could also serve as the recovery framework for an all-hazards approach. The Framework also served to coalesce policy questions that must be addressed for long-term recovery. These questions cover such areas as safety and health, security, financial management, waste management, legal issues, and economic development.

Lesperance, Ann M.; Olson, Jarrod; Stein, Steven L.; Clark, Rebecca; Kelly, Heather; Sheline, Jim; Tietje, Grant; Williamson, Mark; Woodcock, Jody

2011-09-01T23:59:59.000Z

258

Design, set up, and testing of a matrix acidizing apparatus  

E-Print Network [OSTI]

Well stimulation techniques are applied on a regular basis to enhance productivity and maximize recovery in oil and gas wells. Among these techniques, matrix acidizing is probably the most widely performed job because of its relative low cost...

Nevito Gomez, Javier

2006-10-30T23:59:59.000Z

259

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

SciTech Connect (OSTI)

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

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

1995-09-01T23:59:59.000Z

260

Recovery of solvent and by-products from organosolv black liquor  

SciTech Connect (OSTI)

The recovery of alcohol and by-products from ethanol-water and methanol-water pulping liquors was studied. The recovery system proposed consists of three stages: black liquor flashing, lignin precipitation, and precipitation distillation of mother liquor. At the flash stage, 47 and 51% of the alcohol in the black liquor are recovered for ethanol and methanol processes, respectively. The lignin recovery yield at the precipitation stage is 67% for ethanol black liquor and 73% for methanol black liquor. The distillation of precipitation mother liquors enables recovery of 98% ethanol and 96% methanol from this stream as distillate, whereas the distillation residue contains significant amounts of sugars, furfural, and acetic acid that can be recovered. The study concludes with the overall mass balance for the recovery system proposed.

Botello, J.I.; Gilarranz, M.A.; Rodriguez, F.; Oliet, M. [Univ. Complutense de Madrid (Spain). Dept. de Ingenieria Quimica] [Univ. Complutense de Madrid (Spain). Dept. de Ingenieria Quimica

1999-09-01T23:59:59.000Z

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


261

Process for recovery of sulfur from acid gases  

DOE Patents [OSTI]

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

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

1995-01-01T23:59:59.000Z

262

Shock recovery experiments: An assessment  

SciTech Connect (OSTI)

Systematic shock recovery experiments, in which microstructural and mechanical property effects are characterized quantitatively, constitute an important means of increasing our understanding of shock processes. Through studies of the effects of variations in metallurgical and shock loading parameters on structure/property relationships, the micromechanisms of shock deformation, and how they differ from conventional strain rate processes, are beginning to emerge. This paper will highlight the state-of-the-art in shock recovery of metallic and ceramic materials. Techniques will be described which are utilized to ''soft'' recover shock-loaded metallic samples possessing low residual strain; crucial to accurate ''post-mortem'' metallurgical investigations of the influence of shock loading on material behavior. Illustrations of the influence of shock assembly design on the structure/property relationships in shock-recovered copper samples including such issues as residual strain and contact stresses, and their consequences are discussed. Shock recovery techniques used on brittle materials will be reviewed and discussed in light of recent experimental results. Finally, shock recovery structure/property results and VISAR data on the /alpha/--/omega/ shock-induced phase transition in titanium will be used to illustrate the beneficial link between shock recovery and ''real-time'' shock data. 26 refs., 3 figs.

Gray, G.T. III

1989-01-01T23:59:59.000Z

263

{open_quotes}Open vessel{close_quotes} heat balance for TBP-nitric acid solutions  

SciTech Connect (OSTI)

Heat balances were performed for both single phase (organic) and two phase (organic and aqueous) TBP/HNO{sub 3} solutions at temperatures above 100{degrees}C. The balance included the heat produced from oxidation minus losses from evaporation and butylnitrate formation by esterification. Net heat measurements were performed using an isothermal calorimeter. Losses from evaporation were determined from the volume of condensate produced (ice bath trap) and the component concentrate Carbon and nitrogen balances were performed to determine the stoichiometry of the reaction. The heat from oxidation was then calculated using the heats of formation of the reactants and products. Balances were obtained assuming that the heat from esterification was near zero (negligibly small). For two layered reaction systems the net heat was maintained endothermic, and constant with time, due to the transport of water to the organic phase by bubble mixing at the interface. This transported was replaced the water lost in the organic phase by evaporation.

Smith, J.R.; Cavin, W.S.; Laurinat, J.E. [Westinghouse Savannah River Company, Aiken, SC (United States)

1995-12-31T23:59:59.000Z

264

Disposition and transportation of surplus radioactive low specific activity nitric acid. Volume 2, Environmental Assessment  

SciTech Connect (OSTI)

This volume consists of two appendices: public comments and DOE responses, and public comments not requiring responses.

NONE

1995-05-01T23:59:59.000Z

265

FT-IR spectroscopy of nitric acid in TBP/octane solution.  

SciTech Connect (OSTI)

Infrared studies for the HNO{sub 3}/0.73 M TBP n-octane system are reported. Two extracted species, TBP {center_dot} HNO{sub 3} and TBP {center_dot} 2HNO{sub 3}, were identified in the organic phase. The concentration of the individual species was determined by the analysis of the vibrational band at {approx}1650 cm{sup -1}. The band at 1648 cm{sup -1} was assigned to the monosolvate TBP {center_dot} HNO{sub 3} and the band at 1672 cm{sup -1} to the hemisolvate TBP {center_dot} 2HNO{sub 3}. The infrared spectra revealed that with respect to the P{double_bond}O bond, as well to each other, the HNO{sub 3} molecules in the hemisolvate are spectrally non-equivalent. The predominant structure of TBP {center_dot} 2HNO{sub 3} involves the chain HNO{sub 3} dimer. Some ionic NO{sub 3}{sup -} and hydronium ions were identified in this system but only during formation of the monosolvate. The analyses performed in this system can serve for the characterization of HNO{sub 3} in related systems in the presence of metal species.

Ferraro, J. R.; Borkowski, M.; Chiarizia, R.; McAlister, D. R.; Chemistry; Loyola Univ. Chicago

2001-01-01T23:59:59.000Z

266

E-Print Network 3.0 - aqueous nitric acid Sample Search Results  

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

Hall, Sharon J. - School of Life Sciences, Arizona State University Collection: Environmental Sciences and Ecology 3 Standard Operating Procedures Standard Operating Procedures...

267

Recovery | National Nuclear Security Administration  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsrucLas ConchasPassive Solar HomePromising ScienceRecent SREL ReprintsHeaviestRecoveryRecovery |

268

Road to Recovery: Bringing Recovery to Small Town America  

ScienceCinema (OSTI)

The Recovery Act hits the road to reach out to surrounding towns of the Savannah River Site that are struggling with soaring unemployment rates. This project helps recruit thousands of people to new jobs in environmental cleanup at the Savannah River Site.

Nettamo, Paivi

2012-06-14T23:59:59.000Z

269

Solvent Extraction Behavior of Plutonium (IV) Ions in the Presence of Simple Hydroxamic Acids  

SciTech Connect (OSTI)

Formo-and aceto-hydroxamic acids are very effective reagents for stripping Pu(IV) ions from a tri-butyl phosphate phase into nitric acid. Distribution data for Pu(IV) in the presence of these hydroxamate ions have been obtained and trends established. The affinity of aceto-hydroxamic acid for Pu(IV) ions and its selectivity over U(VI) ions is demonstrated by the values of the stability constants in HCIO4. These data support the applications of simple hydroxamic acids in advanced Purex-type solvent extraction systems.

Carrott, M. J.; Fox, O. D.; Maher, C. J.; Mason, C.; Taylor, Robin J.; Sinkov, Sergey I.; Choppin, Gregory R.

2007-11-15T23:59:59.000Z

270

Thermal Stability Of Formohydroxamic Acid  

SciTech Connect (OSTI)

The thermal stability of formohydroxamic acid (FHA) was evaluated to address the potential for exothermic decomposition during storage and its use in the uranium extraction process. Accelerating rate calorimetry showed rapid decomposition at a temperature above 65 {degree}?C; although, the rate of pressure rise was greater than two orders of magnitude less than the lower bound for materials which have no explosive properties with respect to transportation. FHA solutions in water and nitric acid did not reach runaway conditions until 150 {degree}?C. Analysis by differential scanning calorimetry showed that FHA melted at 67 {degree}?C and thermally decomposed at 90 {degree}?C with an enthalpy of -1924 J/g. The energics of the FHA thermal decomposition are comparable to those measured for aqueous solutions of hydroxylamine nitrate. Solid FHA should be stored in a location where the temperature does not exceed 20-25 {degree}?C. As a best practice, the solid material should be stored in a climate-controlled environment such as a refrigerator or freezer. FHA solutions in water are not susceptible to degradation by acid hydrolysis and are the preferred way to handle FHA prior to use.

Fondeur, F. F.; Rudisill, T. S.

2011-10-21T23:59:59.000Z

271

Biosurfactant and enhanced oil recovery  

DOE Patents [OSTI]

A pure culture of Bacillus licheniformis strain JF-2 (ATCC No. 39307) and a process for using said culture and the surfactant lichenysin produced thereby for the enhancement of oil recovery from subterranean formations. Lichenysin is an effective surfactant over a wide range of temperatures, pH's, salt and calcium concentrations.

McInerney, Michael J. (Norman, OK); Jenneman, Gary E. (Norman, OK); Knapp, Roy M. (Norman, OK); Menzie, Donald E. (Norman, OK)

1985-06-11T23:59:59.000Z

272

Turn-on fluorescent probes for detecting nitric oxide in biology  

E-Print Network [OSTI]

Chapter 1. Investigating the Biological Roles of Nitric Oxide and Other Reactive Nitrogen Species Using Fluorescent Probes: This chapter presents an overview of recent progress in the field of reactive nitrogen species ...

McQuade, Lindsey Elizabeth, 1981-

2010-01-01T23:59:59.000Z

273

The detection of nitric oxide and its reactivity with transition metal thiolate complexes  

E-Print Network [OSTI]

Nitric oxide (NO) is a molecule that is essential for life and regulates both beneficial and harmful processes. Because this gaseous radical influences many aspects of health and disease, we wish to explore the relationship ...

Tennyson, Andrew Gregory

2008-01-01T23:59:59.000Z

274

Pathophysiology of endotoxin: microvascular dysfunction, and the roles of VEGF and nitric oxide (NO)  

E-Print Network [OSTI]

PATHOPHYSIOLOGY OF ENDOTOXIN: MICROVASCULAR DYSFUNCTION, AND THE ROLFS OF VEGF AND NITRIC OXIDE (NO) A Senior Honors Thesis bt MARK ANDREW NAFTANFL Submitted to the Olfice of Honors Programs A. Academic Scholarships Texas A&M University ln...

Naftanel, Mark Andrew

2013-02-22T23:59:59.000Z

275

Seminaphthofluorescein-Based Fluorescent Probes for Imaging Nitric Oxide in Live Cells  

E-Print Network [OSTI]

Fluorescent turn-on probes for nitric oxide based on seminaphthofluorescein scaffolds were prepared and spectroscopically characterized. The Cu(II) complexes of these fluorescent probes react with NO under anaerobic ...

Pluth, Michael D.

276

Biochemistry of mobile zinc and nitric oxide revealed by fluorescent sensors  

E-Print Network [OSTI]

Biological mobile zinc and nitric oxide (NO) are two prominent examples of inorganic compounds involved in numerous signaling pathways in living systems. In the past decade, a synergy of regulation, signaling, and translocation ...

Pluth, Michael D.

277

Formic Acid Free Flowsheet Development To Eliminate Catalytic Hydrogen Generation In The Defense Waste Processing  

SciTech Connect (OSTI)

The Defense Waste Processing Facility (DWPF) processes legacy nuclear waste generated at the Savannah River Site (SRS) during production of plutonium and tritium demanded by the Cold War. The nuclear waste is first treated via a complex sequence of controlled chemical reactions and then vitrified into a borosilicate glass form and poured into stainless steel canisters. Converting the nuclear waste into borosilicate glass canisters is a safe, effective way to reduce the volume of the waste and stabilize the radionuclides. Testing was initiated to determine whether the elimination of formic acid from the DWPF's chemical processing flowsheet would eliminate catalytic hydrogen generation. Historically, hydrogen is generated in chemical processing of alkaline High Level Waste sludge in DWPF. In current processing, sludge is combined with nitric and formic acid to neutralize the waste, reduce mercury and manganese, destroy nitrite, and modify (thin) the slurry rheology. The noble metal catalyzed formic acid decomposition produces hydrogen and carbon dioxide. Elimination of formic acid by replacement with glycolic acid has the potential to eliminate the production of catalytic hydrogen. Flowsheet testing was performed to develop the nitric-glycolic acid flowsheet as an alternative to the nitric-formic flowsheet currently being processed at the DWPF. This new flowsheet has shown that mercury can be reduced and removed by steam stripping in DWPF with no catalytic hydrogen generation. All processing objectives were also met, including greatly reducing the Slurry Mix Evaporator (SME) product yield stress as compared to the baseline nitric/formic flowsheet. Ten DWPF tests were performed with nonradioactive simulants designed to cover a broad compositional range. No hydrogen was generated in testing without formic acid.

Lambert, Dan P.; Stone, Michael E.; Newell, J. David; Fellinger, Terri L.; Bricker, Jonathan M.

2012-09-14T23:59:59.000Z

278

Department of Energy Recovery Act Investment in Biomass Technologies...  

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

Department of Energy Recovery Act Investment in Biomass Technologies Department of Energy Recovery Act Investment in Biomass Technologies The American Recovery and Reinvestment Act...

279

Opportunities and Challenges of Thermoelectrlic Waste Heat Recovery...  

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

for Automotive Waste Heat Recovery Develop Thermoelectric Technology for Automotive Waste Heat Recovery Thermoelectric Generator Development for Automotive Waste Heat Recovery...

280

Department of Energy Completes Five Recovery Act Projects - Moves...  

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

Five Recovery Act Projects - Moves Closer to Completing Recovery Act Funded Work at Oak Ridge Site Department of Energy Completes Five Recovery Act Projects - Moves Closer to...

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


281

Recovery Act: Clean Coal Power Initiative | Department of Energy  

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

Recovery Act: Clean Coal Power Initiative Recovery Act: Clean Coal Power Initiative A report detailling the Clean Coal Power initiative funded under the American Recovery and...

282

The catalytic reduction of nitric oxide with ammonia over tetraamminecopper (II) complexes  

E-Print Network [OSTI]

primary goal has been to develop catalysts that will promote selective reduction of nitric oxide to nitrogen with various reducing agents. The use of metals and mixed metal oxide catalysts with reducing agents such as hydrogen, car- bon monoxide... the energy of the v* orbital of NO in relationship to tne energies 11, 12 of the d orbitals of the metal. ' Although nitric oxide is thermo- dynamically unstable, with respect to decomposition to nitrogen and The citations of the following cages follow...

Oates, Margaret Deron

1979-01-01T23:59:59.000Z

283

Arsenic toxicity induced endothelial dysfunction and dementia: Pharmacological interdiction by histone deacetylase and inducible nitric oxide synthase inhibitors  

SciTech Connect (OSTI)

Arsenic toxicity has been reported to damage all the major organs including the brain and vasculature. Dementia including Alzheimer's disease (AD) and vascular dementia (VaD) are posing greater risk to the world population as it is now increasing at a faster rate. We have investigated the role of sodium butyrate, a selective histone deacetylase (HDAC) inhibitor and aminoguanidine, a selective inducible nitric oxide synthase (iNOS) inhibitor in pharmacological interdiction of arsenic toxicity induced vascular endothelial dysfunction and dementia in rats. Arsenic toxicity was done by administering arsenic drinking water to rats. Morris water-maze (MWM) test was used for assessment of learning and memory. Endothelial function was assessed using student physiograph. Oxidative stress (aortic superoxide anion, serum and brain thiobarbituric acid reactive species, brain glutathione) and nitric oxide levels (serum nitrite/nitrate) were also measured. Arsenic treated rats have shown impairment of endothelial function, learning and memory, reduction in serum nitrite/nitrate and brain GSH levels along with increase in serum and brain TBARS. Sodium butyrate as well as aminoguanidine significantly convalesce arsenic induced impairment of learning, memory, endothelial function, and alterations in various biochemical parameters. It may be concluded that arsenic induces endothelial dysfunction and dementia, whereas, sodium butyrate, a HDAC inhibitor as well as aminoguanidine, a selective iNOS inhibitor may be considered as potential agents for the management of arsenic induced endothelial dysfunction and dementia. - Highlights: • As has induced endothelial dysfunction (Edf) and vascular dementia (VaD). • As has increased oxidative stress, AChE activity and decreased serum NO. • Inhibitors of HDAC and iNOS have attenuated As induced Edf and VaD. • Both the inhibitors have attenuated As induced biochemical changes. • Inhibitor of HDAC and iNOS has shown good potential in As induced VaD.

Sharma, Bhupesh, E-mail: drbhupeshresearch@gmail.com; Sharma, P.M.

2013-11-15T23:59:59.000Z

284

Bioelectrochemical Integration of Waste Heat Recovery, Waste...  

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

electrolytic cell, designed to integrate waste heat recovery (i.e a microbial heat recovery cell or MHRC), can operate as a fuel cell and convert effluent streams into...

285

Flare Gas Recovery in Shell Canada Refineries  

E-Print Network [OSTI]

Two of Shell Canada's refineries have logged about six years total operating experience with modern flare gas recovery facilities. The flare gas recovery systems were designed to recover the normal continuous flare gas flow for use in the refinery...

Allen, G. D.; Wey, R. E.; Chan, H. H.

1983-01-01T23:59:59.000Z

286

Automated intrusion recovery for web applications  

E-Print Network [OSTI]

In this dissertation, we develop recovery techniques for web applications and demonstrate that automated recovery from intrusions and user mistakes is practical as well as effective. Web applications play a critical role ...

Chandra, Ramesh, Ph. D. Massachusetts Institute of Technology

2013-01-01T23:59:59.000Z

287

HVAC Energy Recovery Design and Economic Evaluation  

E-Print Network [OSTI]

ENRECO has prepared this paper on HVAC energy recovery to provide the engineer with an overview of the design engineering as well as the economic analysis considerations necessary to evaluate the potential benefits of energy recovery....

Kinnier, R. J.

1979-01-01T23:59:59.000Z

288

RECYCLING OF CdTe PHOTOVOLTAIC MODULES: RECOVERY OF CADMIUM AND TELLURIUM Vasilis Fthenakis1, Paul Duby2, Wenming Wang1, Christopher Graves2 & Anuta Belova2  

E-Print Network [OSTI]

RECYCLING OF CdTe PHOTOVOLTAIC MODULES: RECOVERY OF CADMIUM AND TELLURIUM Vasilis Fthenakis1, Paul the recovery of tellurium. Keywords: Photovoltaic, Recycling, CdTe 1. INTRODUCTION Photovoltaic modules acid (sulfuric) /hydrogen peroxide solution mixture to generate a solution that is rich in cadmium

289

Nitric oxide emissions from the high-temperature viscous boundary layers of hypersonic aircraft within the stratosphere  

SciTech Connect (OSTI)

The authors study the nitric oxide emission characteristics of supersonic aircraft resulting from heating of viscous boundary layers along the skin of the aircraft. Previous study has concentrated on nitric oxide emissions coming from combustion products from the scramjet engines. This work shows that above mach 8, emissions from viscous heating become a significant factor in total emission of nitric oxide. Above mach 16 it becomes the dominant source of emission.

Brooks, S.B.; Lewis, M.J.; Dickerson, R.R. [Univ. of Maryland, College Park, MD (United States)

1993-09-20T23:59:59.000Z

290

Enhanced oil recovery in Rumania  

SciTech Connect (OSTI)

The paper describes the application of the fire-floods to a broad range of Romanian oil reservoirs and crude properties and reviews the field tests of polymer flooding, surfactant flooding and alkaline flooding. A commercial scale project with cyclic steam injection is presented and also the use of the domestic CO/sub 2/ sources to enhanced oil recovery. The results and the difficulties encountered are briefly discussed and also the potential of EOR methods in Romania are presented. 17 refs.

Carcoana, A.N.

1982-01-01T23:59:59.000Z

291

Recovery Act | Department of Energy  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious Rank EERE: AlternativeEnvironment,Institutes and Launches theResidentialRecovery Act State SummariesPast

292

State Agency Recovery Act Funding  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious RankCombustion |Energy Usage » SearchEnergyDepartmentScopingOverview *Agency Recovery Act Funding .Alabama

293

Responsive copolymers for enhanced petroleum recovery. Quarterly technical progress report, December 21, 1994--March 22, 1995  

SciTech Connect (OSTI)

The purpose of this study is to extend the concept of micellar polymerization to more complex systems, and to explore the responsive nature of hydrophobically modified polyelectrolytes by tailoring the microstructure. The synthesis of hydrophobically modified acrylamide/acrylic acid copolymer is described. These types of polymers are of interest as thickening agents utilized in enhanced oil recovery.

McCormick, C.; Hester, R.

1995-05-01T23:59:59.000Z

294

Enhanced oil recovery in Rumania  

SciTech Connect (OSTI)

The wide oil field experience of the Romanian oil men in producing hydrocarbon reservoirs is based on an old tradition, but only after 1945 reservoir engineering studies were started in Romania. Beginning with 1950 conventional recovery methods expanded continually. During the last 10 years, however, the crude oil, as energy resource, has become of tremendous importance. The need for increasing the ultimate oil recovery has been felt in Romania as everywhere else. To attain this goal EOR methods were and are tested and expanded on a commercial scale. The paper describes the application of the fire-floods to a broad range of Romanian oil reservoirs and crude properties and reviews the field tests of polymer flooding, surfactant flooding and alkaline flooding. A commercial scale project with cyclic steam injection is presented and also the use of the domestic CO/sub 2/ sources to enhance oil recovery. The results and the diffuculties encountered are briefly discussed and also the potential of EOR methods in Romania are presented.

Carcoana, A.N.

1982-01-01T23:59:59.000Z

295

Recovery Act ? An Interdisciplinary Program for Education and...  

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

Recovery Act An Interdisciplinary Program for Education and Outreach in Transportation Electrification Recovery Act An Interdisciplinary Program for Education and...

296

Diesel Engine Waste Heat Recovery Utilizing Electric Turbocompound...  

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

More Documents & Publications Diesel Engine Waste Heat Recovery Utilizing Electric Trubocompound Technology Diesel Engine Waste Heat Recovery Utilizing Electric...

297

Synergistic air port corrosion in kraft recovery boilers  

SciTech Connect (OSTI)

Localized hot corrosion can occur on the cold-side of air-ports in Kraft recovery boilers. Depending on the basicity of the molten salt, either acidic or basic fluxing takes place, with a solubility minima at the transition between the two reactions. For stainless steel, if the basicity of the fused salt is between the iron and chromium oxide solubility minima, then a synergistic effect can occur that leads to rapid corrosion. The products of one reaction are the reactants of the other, which eliminates the need for rate-controlling diffusion. This effect can explain why stainless steel is attacked more readily than carbon steel.

Holcomb, Gordon R.

2001-08-01T23:59:59.000Z

298

Reductive stripping process for uranium recovery from organic extracts  

DOE Patents [OSTI]

In the reductive stripping of uranium from an organic extractant in a uranium recovery process, the use of phosphoric acid having a molarity in the range of 8 to 10 increases the efficiency of the reductive stripping and allows the strip step to operate with lower aqueous to organic recycle ratios and shorter retention time in the mixer stages. Under these operating conditions, less solvent is required in the process, and smaller, less expensive process equipment can be utilized. The high strength H/sub 3/PO/sub 4/ is available from the evaporator stage of the process.

Hurst, F.J. Jr.

1983-06-16T23:59:59.000Z

299

Superior catalysts for selective catalytic reduction of nitric oxide. Quarterly technical progress report, April 1, 1995--June 30, 1995  

SciTech Connect (OSTI)

Efforts continued towards the synthesis of new pillared clay catalysts for the selective catalytic reduction of nitric oxide by ammonia. The possibility of utilizing hydrocarbons was also investigated.

Li, W.B.; Yang, R.T.

1995-12-01T23:59:59.000Z

300

Kraft recovery boiler physical and chemical processes  

SciTech Connect (OSTI)

The focus of this book is on the recent research into the physical and chemical processes occurring in and around a black liquor recovery boiler. Almost all of the detailed technical information in this book has previously appeared in the open literature. The purpose here is not to present research for the first time, but to present it in a context of the other processes occurring in recovery boilers. Topics covered include: general characteristics of recovery boilers; black liquor thermal and transport properties; black liquor droplet formation and combustion; recovery boiler char bed processes; flow and mixing in Kraft recovery boilers; entrainment and carryover in recovery furnaces; fume formation and dust chemistry; deposits and boiler plugging; and recovery boiler thermal performance. 257 refs., 102 figs., 38 tabs.

Adams, T.N.; Frederick, W.J. (Adams (Terry N.), Tacoma, WA (USA); Oregon State Univ., Corvallis, OR (USA). Dept. of Chemical Engineering)

1988-01-01T23:59:59.000Z

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


301

Endothelial-constitutive nitric oxide synthase exists in airways and diesel exhaust particles inhibit the effect of nitric oxide  

SciTech Connect (OSTI)

Diesel exhaust particles (DEP) are an important cause of air pollution and are thought to be responsible for some respiratory ailments, but the exact mechanism is not known. We evaluated whether DEP inhibit nitric oxide (NO) synthesis in bronchi as No is present in the exhaled air and has a physiological role in the respiratory tract. Aortic rings were also examined for comparison. We observed that acetylcholine (ACh) induced contraction of the bronchi was partially attenuated by the simultaneous release of NO. When bronchial rings were incubated either with N{sup G}-methyl-L-arginine (L-NMA): an inhibitor of NO synthase (NOS) or with DEP, the contraction to ACh was abolished. The source of the NOS was the bronchial epithelium and this endothelial-constitutive NOS was demonstrated by immunohistochemistry. DEP like L-NMA inhibited the ACh induced endothelium dependent relaxation in the aortic rings. The inhibition of NO release by DEP and L-NMA from bronchial and aortic rings was also confirmed by a selective NO electrode. We conclude that inhibition of NO availability by DEP may in part be responsible for the adverse respiratory effects seen by inhalation of these particles in polluted air. 27 refs., 6 figs.

Muto, Emiko; Hayashi, Toshio; Yamada, Kazuyoshi [Nagoya Univ. School of Medicine (Japan)] [and others] [Nagoya Univ. School of Medicine (Japan); and others

1996-12-31T23:59:59.000Z

302

The hydrogenation of dietary unsaturated fatty acids by the ruminant  

E-Print Network [OSTI]

LIBRARY g 4 M COLLEGE Pf TEXIIG THE HYDROGENATION OF DIETARY UNSATURATED FATTY ACIDS SY THE RUMINANT A The sis H. G. RAMAKRISHNA REDDY Submitted to the Graduate School of the Agni cultural and Mechanical College of Texas in partial... EXTRACTION AND RECOVERY OF FATTY AC IDS FATTY ACID ANALYSES . RESULTS AND DISCUSSION Cottonseed oil fed goats. Linseed oil fed goats. SUMMARY AND CONCLUSIONS. LITERATURE CITED. 17 LIST OF TAIILXS Page I, Typical Component Acids (Wts. psr cent...

Reddy, H. G. Ramakrishna

2012-06-07T23:59:59.000Z

303

USDOE Innovative Clean Coal Technology Demonstration Project: Passamaquoddy Technology Recovery Scrubber{trademark}. Final report: Volume 1  

SciTech Connect (OSTI)

This Final Report provides available design, operational, and maintenance information, and marketing plans, on the Passamaquoddy Technology Recovery Scrubber{trademark} demonstration Project at the Dragon Products company`s cement plant at Thomaston, Maine. In addition, data on pollutant removal efficiencies and system economics are reviewed. The Recovery Scrubber was developed to simultaneously address the emission of acid gas pollutants and the disposal of alkaline solid waste at a cement plant. The process, however, has general application to other combustion processes including waste or fossil fuel fired boilers. Selected chemistry of the exhaust gas, (before and after treatment by the Recovery Scrubber), selected chemistry of the cement plant kiln baghouse dust catch (before and after treatment by the Recovery Scrubber), and Dragon cement plant economics are presented. current marketing efforts and potential markets for the Recovery Scrubber in several industries are discussed.

Not Available

1994-02-01T23:59:59.000Z

304

Acidic dissolution behavior of U containing ZrO2–MgO ceramics  

SciTech Connect (OSTI)

This study explores the possibility of dissolving zirconia-magnesia inert matrix fuel containing uranium oxide as a fissile material and plutonium homolog and erbium oxide as a burnable poison with nitric and sulfuric acid as a potential first step in a reprocessing scheme. The progress of the dissolution is followed by monitoring the amount of material in solution by inductively coupled plasma-atomic emission spectroscopy, assessing the speciation of the material by time resolved laser fluorescence spectroscopy, and determining and quantifying the crystalline phases present in the remaining residue by X-ray diffraction. This study has shown a linear incongruent dissolution of the cubic zirconia phase in concentrated nitric acid under certain chemical compositions, while the magnesium oxide phase is completely soluble. In sulfuric acid uranium, erbium, and magnesium are soluble to different extents while zirconium forms a colloidal suspension that conglomerates and settles out of solution. The feasibility of the dissolution of zirconia-magnesia inert matrix fuel with nitric and sulfuric acid for reprocessing is discussed.

Kiel Holliday; Nicholas Smith; Thomas Hartmann; Gary Cerefice; Ken Czerwinski

2011-11-01T23:59:59.000Z

305

The Hanford Story: Recovery Act  

Broader source: Energy.gov [DOE]

This is the third chapter of The Hanford Story. This chapter is a tribute to the thousands of workers and representatives of regulatory agencies, neighboring states, Tribes, stakeholders, and surrounding communities who came together to put stimulus funding to work at Hanford. The video describes how the Department of Energy and its contractors turned a nearly $2 billion investment of American Recovery and Reinvestment Act funding in 2009 into nearly $4 billion worth of environmental cleanup work over the past two years. At the same time, Hanford workers have reduced the cleanup footprint of the Hanford Site by more than half (586 square miles to 241 sq. mi. through August -- 59 percent).

306

EVALUATION OF POTENTIAL ELUANTS FOR NON-ACID ELUTION OF CESIUM FROM RESORCINOL-FORMALDEHYDE RESIN  

SciTech Connect (OSTI)

Small-column ion exchange (SCIX) units installed in high-level waste tanks to remove Cs-137 from highly alkaline salt solutions are among the waste treatment plans in the DOE-complex. Spherical Resorcinol-Formaldehyde (sRF) is the ion exchange resin selected for use in the Hanford Waste Treatment and Immobilization Plant (WTP). It is also the primary ion exchange material under consideration for SCIX at the Hanford site. The elution step of the multi-step ion exchange process is typically done with 0.5 M nitric acid. An acid eluant is a potential hazard in the event of a spill, leak, etc. because the high-level waste tanks are made of carbon steel. Corrosion and associated structural damage may ensue. A study has been conducted to explore non-acid elution as an alternative. Batch contact sorption equilibrium screening tests have been conducted with 36 potential non-acid eluants. The sorption tests involve equilibrating each cesium-containing eluant solution with the sRF resin for 48 hours at 25 C in a shaker oven. In the sorption tests, an eluant is deemed to have a high cesium elution potential if it minimizes cesium sorption onto the sRF resin. The top candidates (based on lowest cesium sorption distribution coefficients) include ammonium carbonate, ammonium carbonate/ammonium hydroxide, ammonium bicarbonate, rubidium carbonate, ammonium acetate, ammonium acetate/ammonium hydroxide, ammonium bicarbonate/ammonium hydroxide, calcium chloride, and magnesium chloride. A select few of the top candidate eluants from the screening tests were subjected to actual sorption (loading) and elution tests to confirm their elution ability. The actual sorption (loading) and elution tests mimicked the typical sRF-cesium ion exchange process (i.e., sorption or loading, caustic wash, water rinse, and elution) via batch contact sorption and quasi column caustic wash/water rinse/elution. The eluants tested included ammonium carbonate, ammonium acetate, calcium acetate, magnesium acetate, and nitric acid. Calcium acetate and magnesium acetate were substitutes for calcium chloride and magnesium chloride respectively due to corrosion concerns. Nitric acid was selected for benchmarking since it is the baseline cesium eluant for sRF resin. The cesium elution performance of ammonium carbonate and ammonium acetate was approximately the same as the benchmark eluant, nitric acid. Ninety-seven (97), 94, and 100% percent of the cesium sorbed or loaded were eluted by ammonium carbonate, ammonium acetate, and nitric acid was respectively. The performance of calcium acetate and magnesium acetate, on the other hand, was mediocre. Percent elution was 16 and 8 respectively.

Adu-Wusu, K.; Pennebaker, F.

2010-12-22T23:59:59.000Z

307

Recovery from chemical, biological, and radiological incidents :  

SciTech Connect (OSTI)

To restore regional lifeline services and economic activity as quickly as possible after a chemical, biological or radiological incident, emergency planners and managers will need to prioritize critical infrastructure across many sectors for restoration. In parallel, state and local governments will need to identify and implement measures to promote reoccupation and economy recovery in the region. This document provides guidance on predisaster planning for two of the National Disaster Recovery Framework Recovery Support Functions: Infrastructure Systems and Economic Recovery. It identifies key considerations for infrastructure restoration, outlines a process for prioritizing critical infrastructure for restoration, and identifies critical considerations for promoting regional economic recovery following a widearea disaster. Its goal is to equip members of the emergency preparedness community to systematically prioritize critical infrastructure for restoration, and to develop effective economic recovery plans in preparation for a widearea CBR disaster.

Franco, David Oliver; Yang, Lynn I.; Hammer, Ann E.

2012-06-01T23:59:59.000Z

308

Transformation of Resources to Reserves: Next Generation Heavy-Oil Recovery Techniques  

SciTech Connect (OSTI)

This final report and technical progress report describes work performed from October 1, 2004 through September 30, 2007 for the project 'Transformation of Resources to Reserves: Next Generation Heavy Oil Recovery Techniques', DE-FC26-04NT15526. Critical year 3 activities of this project were not undertaken because of reduced funding to the DOE Oil Program despite timely submission of a continuation package and progress on year 1 and 2 subtasks. A small amount of carried-over funds were used during June-August 2007 to complete some work in the area of foamed-gas mobility control. Completion of Year 3 activities and tasks would have led to a more thorough completion of the project and attainment of project goals. This progress report serves as a summary of activities and accomplishments for years 1 and 2. Experiments, theory development, and numerical modeling were employed to elucidate heavy-oil production mechanisms that provide the technical foundations for producing efficiently the abundant, discovered heavy-oil resources of the U.S. that are not accessible with current technology and recovery techniques. Work fell into two task areas: cold production of heavy oils and thermal recovery. Despite the emerging critical importance of the waterflooding of viscous oil in cold environments, work in this area was never sanctioned under this project. It is envisioned that heavy oil production is impacted by development of an understanding of the reservoir and reservoir fluid conditions leading to so-called foamy oil behavior, i.e, heavy-oil solution gas drive. This understanding should allow primary, cold production of heavy and viscous oils to be optimized. Accordingly, we evaluated the oil-phase chemistry of crude oil samples from Venezuela that give effective production by the heavy-oil solution gas drive mechanism. Laboratory-scale experiments show that recovery correlates with asphaltene contents as well as the so-called acid number (AN) and base number (BN) of the crude oil. A significant number of laboratory-scale tests were made to evaluate the solution gas drive potential of West Sak (AK) viscous oil. The West Sak sample has a low acid number, low asphaltene content, and does not appear foamy under laboratory conditions. Tests show primary recovery of about 22% of the original oil in place under a variety of conditions. The acid number of other Alaskan North Slope samples tests is greater, indicating a greater potential for recovery by heavy-oil solution gas drive. Effective cold production leads to reservoir pressure depletion that eases the implementation of thermal recovery processes. When viewed from a reservoir perspective, thermal recovery is the enhanced recovery method of choice for viscous and heavy oils because of the significant viscosity reduction that accompanies the heating of oil. One significant issue accompanying thermal recovery in cold environments is wellbore heat losses. Initial work on thermal recovery found that a technology base for delivering steam, other hot fluids, and electrical heat through cold subsurface environments, such as permafrost, was in place. No commercially available technologies are available, however. Nevertheless, the enabling technology of superinsulated wells appears to be realized. Thermal subtasks focused on a suite of enhanced recovery options tailored to various reservoir conditions. Generally, electrothermal, conventional steam-based, and thermal gravity drainage enhanced oil recovery techniques appear to be applicable to 'prime' Ugnu reservoir conditions to the extent that reservoir architecture and fluid conditions are modeled faithfully here. The extent of reservoir layering, vertical communication, and subsurface steam distribution are important factors affecting recovery. Distribution of steam throughout reservoir volume is a significant issue facing thermal recovery. Various activities addressed aspects of steam emplacement. Notably, hydraulic fracturing of horizontal steam injection wells and implementation of steam trap control that limits steam entry into hor

Stanford University; Department of Energy Resources Engineering Green Earth Sciences

2007-09-30T23:59:59.000Z

309

CALIFORNIA RECOVERY ACT SNAPSHOT | Department of Energy  

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

has substantial natural resources, including oil, gas, solar, wind, geothermal, and hydroelectric power .The American Recovery & Reinvestment Act (ARRA) is making a meaningful down...

310

Clean Cities Recovery Act: Vehicle & Infrastructure Deployment  

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

project through collection of vehicle, infrastructure and training information. RELEVANCE Alternative Fuel & Advance Technology Vehicles Pilot Program Clean Cities Recovery Act:...

311

American Recovery and Reinvestment Act, Financial Assistance...  

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

- ARRAAttachment3.rtf FOIA Frequently Requested Documents: DE-EE0002884 Recovery Act - Integrated Algal Biorefinery (IABR) Financial Assistance Funding Opportunity Announcement...

312

Faces of the Recovery Act: 1366 Technologies  

Broader source: Energy.gov [DOE]

LEXINGTON, MA - At 1366 Technologies, Ely Sachs and Frank van Mierlo are using ARPA-E Recovery Act funding to dramatically reduce the costs of solar panel production.

313

Weatherization Formula Grants - American Recovery and Reinvestment...  

Energy Savers [EERE]

Act of 2009 waprecoveryactfoa.pdf More Documents & Publications Microsoft Word - nDE-FOA-0000051.rtf Weatherization Formula Grants - American Recovery and Reinvestment Act...

314

Bioelectrochemical Integration of Waste Heat Recovery, Waste...  

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

MHRC System Concept ADVANCED MANUFACTURING OFFICE Bioelectrochemical Integration of Waste Heat Recovery, Waste-to-Energy Conversion, and Waste-to-Chemical Conversion with...

315

Recovery Act Progress Update: Reactor Closure Feature  

SciTech Connect (OSTI)

A Recovery Act Progress Update. Decommissioning of two nuclear reactor sites at the Department of Energy's facilities has been approved and is underway.

Cody, Tom

2010-01-01T23:59:59.000Z

316

Recovery Act Progress Update: Reactor Closure Feature  

ScienceCinema (OSTI)

A Recovery Act Progress Update. Decommissioning of two nuclear reactor sites at the Department of Energy's facilities has been approved and is underway.

Cody, Tom

2012-06-14T23:59:59.000Z

317

Optimize carbon dioxide sequestration, enhance oil recovery  

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

Optimize carbon dioxide sequestration, enhance oil recovery The simulation provides an important approach to estimate the potential of storing carbon dioxide in depleted oil fields...

318

Metal recovery from porous materials  

DOE Patents [OSTI]

A method for recovering plutonium and other metals from materials by leaching comprising the steps of incinerating the materials to form a porous matrix as the residue of incineration, immersing the matrix into acid in a microwave-transparent pressure vessel, sealing the pressure vessel, and applying microwaves so that the temperature and the pressure in the pressure vessel increase. The acid for recovering plutonium can be a mixture of HBF.sub.4 and HNO.sub.3 and preferably the pressure is increased to at least 100 PSI and the temperature to at least 200.degree. C. The porous material can be pulverized before immersion to further increase the leach rate.

Sturcken, Edward F. (P.O. Box 900, Isle of Palms, SC 29451)

1992-01-01T23:59:59.000Z

319

INT. J. CONTROL, 1989, VOL. 49, NO. 4, 1249 1271 Loop recovery via Hm/* sensitivity recovery  

E-Print Network [OSTI]

;1250 J. B. Moore and T T Tay context of Anderson and Moore ( 1971 ) and Kwakernaak and Sivan ( 1972INT. J. CONTROL, 1989, VOL. 49, NO. 4, 1249­ 1271 Loop recovery via Hm/* sensitivity recovery J. B. MOOREt and T. T. TAY~ Loop transfer recovery (LTR) techniques are known to enhance the input or output

Moore, John Barratt

320

Method for enhanced oil recovery  

DOE Patents [OSTI]

The present invention is directed to an improved method for enhanced recovery of oil from relatively "cold" reservoirs by carbon dioxide flooding. In oil reservoirs at a temperature less than the critical temperature of 87.7.degree. F. and at a pore pressure greater than the saturation pressure of carbon dioxide at the temperature of the reservoir, the carbon dioxide remains in the liquid state which does not satisfactorily mix with the oil. However, applicants have found that carbon dioxide can be vaporized in situ in the reservoir by selectively reducing the pore pressure in the reservoir to a value less than the particular saturated vapor pressure so as to greatly enhance the mixing of the carbon dioxide with the oil.

Comberiati, Joseph R. (Morgantown, WV); Locke, Charles D. (Morgantown, WV); Kamath, Krishna I. (Chicago, IL)

1980-01-01T23:59:59.000Z

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


321

Enhanced oil recovery using hydrogen peroxide injection  

SciTech Connect (OSTI)

NOVATEC received an US Patent on a novel method to recovery viscous oil by hydrogen peroxide injection. The process appears to offer several significant improvements over existing thermal methods of oil recovery. Tejas joined NOVATEC to test the process in the laboratory and to develop oil field applications and procedures.

Moss, J.T. Jr.; Moss, J.T.

1995-02-01T23:59:59.000Z

322

Thermal recovery of oil and bitumen  

SciTech Connect (OSTI)

This book is organized into the following chapters: Introduction to Thermal Recovery; Conduction of Heat Within Solids; Convective Heating within Reservoirs; Steamfloodings; The Displacement of Heavy Oil; Cyclic Steam Simulation; Steam-Assisted Gravity Drainage; Steam Recovery Equipment and Facilities; and In Situ Combustion.

Butler, R.M. (Dept. of Chemical and Petroleum Engineering, Univ. of Calgary, Calgary, Alberta (CA))

1991-01-01T23:59:59.000Z

323

Faces of the Recovery Act: Sun Catalytix  

ScienceCinema (OSTI)

BOSTON- At the Massachusetts Institute of Technology, Dan Nocera talks about Sun Catalytix, the next generation of solar energy, and ARPA-E funding through the Recovery Act. To learn about more ARPA-E projects through the Recovery Act: http://arpa-e.energy.gov/FundedProjects.aspx

Nocera, Dave

2013-05-29T23:59:59.000Z

324

Optimize carbon dioxide sequestration, enhance oil recovery  

E-Print Network [OSTI]

- 1 - Optimize carbon dioxide sequestration, enhance oil recovery January 8, 2014 Los Alamos simulation to optimize carbon dioxide (CO2) sequestration and enhance oil recovery (CO2-EOR) based on known production. Due to carbon capture and storage technology advances, prolonged high oil prices

325

Chemical Degradation Studies on a Series of Dithiophosphinic Acids  

SciTech Connect (OSTI)

A significant increase in the stability of a series of dithiophosphinic acids (DPAHs) under oxidizing acidic conditions was achieved. The degradation behavior of a series of DPAHs, designed for lanthanide/actinide separation, was examined. The stability of the DPAHs, when contacted with varying nitric acid concentrations, was tested and monitored using 31P {1H} NMR. Changes in the functional groups of the DPAHs resulted in substantial increases in the stability. However, when placed in contact with 2 M HNO3 all the DPAHs eventually showed signs of degradation. The addition of a radical scavenger, hydrazine, inhibited the degradation of the DPAHs. In the presence of a small concentration of hydrazine, five of the DPAHs remained stable for over a month in direct contact with 2 M HNO3.

Melissa E. Freiderich; Dean R. Peterman; John R. Klaehn; Philippe Marc; Laetitia H. Delmau

2014-04-01T23:59:59.000Z

326

Kudzu (Pueraria montana) invasion doubles emissions of nitric oxide and increases ozone pollution  

E-Print Network [OSTI]

Kudzu (Pueraria montana) invasion doubles emissions of nitric oxide and increases ozone pollution) The nitrogen-fixing legume kudzu (Pueraria montana) is a wide- spread invasive plant in the southeastern United the effects of kudzu invasions on soils and trace N gas emissions at three sites in Madison County, Georgia

Mickley, Loretta J.

327

Nitric Oxide Production from Surface Recombination of Oxygen and Nitrogen Atoms  

E-Print Network [OSTI]

of hypersonic reentry vehicles. In the Earth's atmosphere, oxygen and nitrogen atoms are generated in the shock1 Nitric Oxide Production from Surface Recombination of Oxygen and Nitrogen Atoms Dusan A. Pejakovi from the recombination of oxygen and nitrogen atoms on quartz. The experiments employ two-photon laser

Martín, Pino

328

Kinetic modeling of nitric oxide removal from exhaust gases by Selective Non-Catalytic Reduction  

E-Print Network [OSTI]

for increased pressure predict a wider temperature range at which significant nitric oxide can be removed and also in the case of RAPRENOx process the levels of N20 (a by-product in the case of the RAPRENOx process) are significantly lower. The accounting...

Chenanda, Cariappa Mudappa

2012-06-07T23:59:59.000Z

329

Joule heating and nitric oxide in the thermosphere, 2 Charles A. Barth1  

E-Print Network [OSTI]

Joule heating and nitric oxide in the thermosphere, 2 Charles A. Barth1 Received 14 April 2010, gravity waves propagate from the polar regions toward the equator heating the thermosphere at 140 km and higher. These gravity waves are produced by Joule heating that occurs at latitudes of 60° and higher

Bailey, Scott

330

Modeling gas phase nitric oxide release in lung epithelial cells Jingjing Jiang a  

E-Print Network [OSTI]

Modeling gas phase nitric oxide release in lung epithelial cells Jingjing Jiang a , Steven C- dated our model with experimental results of gas phase NO release and intracellular L enzyme on NO production. Our model predicts intracellular L-arginine and gas phase NO release over a wide

George, Steven C.

331

Method for magnesium sulfate recovery  

DOE Patents [OSTI]

A method of obtaining magnesium sulfate substantially free from radioactive uranium from a slag containing the same and having a radioactivity level of at least about 7000 pCi/gm. The slag is ground to a particle size of about 200 microns or less. The ground slag is then contacted with a concentrated sulfuric acid under certain prescribed conditions to produce a liquid product and a solid product. The particulate solid product and a minor amount of the liquid is then treated to produce a solid residue consisting essentially of magnesium sulfate substantially free of uranium and having a residual radioactivity level of less than 1000 pCi/gm. In accordance with the preferred embodiment of the invention, a catalyst and an oxidizing agent are used during the initial acid treatment and a final solid residue has a radioactivity level of less than about 50 pCi/gm.

Gay, Richard L. (Canoga Park, CA); Grantham, LeRoy F. (Calabasas, CA)

1987-01-01T23:59:59.000Z

332

Method for magnesium sulfate recovery  

DOE Patents [OSTI]

A method is described for obtaining magnesium sulfate substantially free from radioactive uranium from a slag containing the same and having a radioactivity level of at least about 7,000 pCi/gm. The slag is ground to a particle size of about 200 microns or less. The ground slag is then contacted with a concentrated sulfuric acid under certain prescribed conditions to produce a liquid product and a solid product. The particulate solid product and a minor amount of the liquid is then treated to produce a solid residue consisting essentially of magnesium sulfate substantially free of uranium and having a residual radioactivity level of less than 1,000 pCi/gm. In accordance with the preferred embodiment of the invention, a catalyst and an oxidizing agent are used during the initial acid treatment and a final solid residue has a radioactivity level of less than about 50 pCi/gm.

Gay, R.L.; Grantham, L.F.

1987-08-25T23:59:59.000Z

333

Metal recovery from porous materials  

DOE Patents [OSTI]

A method is described for recovering plutonium and other metals from materials by leaching comprising the steps of incinerating the materials to form a porous matrix as the residue of incineration, immersing the matrix into acid in a microwave-transparent pressure vessel, sealing the pressure vessel, and applying microwaves so that the temperature and the pressure in the pressure vessel increase. The acid for recovering plutonium can be a mixture of HBF[sub 4] and HNO[sub 3] and preferably the pressure is increased to at least 100 PSI and the temperature to at least 200 C. The porous material can be pulverized before immersion to further increase the leach rate.

Sturcken, E.F.

1992-10-13T23:59:59.000Z

334

Researching power plant water recovery  

SciTech Connect (OSTI)

A range of projects supported by NETl under the Innovations for Existing Plant Program are investigating modifications to power plant cooling systems for reducing water loss, and recovering water from the flue gas and the cooling tower. This paper discusses two technologies showing particular promise condense water that is typically lost to evaporation, SPX technologies' Air2Air{sup trademark} condenses water from a cooling tower, while Lehigh University's process condenses water and acid in flue gas. 3 figs.

NONE

2008-04-01T23:59:59.000Z

335

An algorithm for recovery of distributed applications with directed dependencies  

E-Print Network [OSTI]

recovery. The thesis proposes a distributed algorithm which coordinates management entities, called agents, to monitor the managed resources (which have directed failure and recovery dependencies among them) and perform recovery actions once failures have...

Yang, Jiantian

1996-01-01T23:59:59.000Z

336

Hanford Information Related to the American Recovery and Reinvestment...  

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

Recovery Act of 2009 Recovery Act of 2009 Recovery Act of 2009 Hanford ARRA FAQ Hanford ARRA Weekly Reports Hanford ARRA News Hanford ARRA Photogallery Hanford ARRA Videos Hanford...

337

NORTHEASTERN NATURALIST2008 15(3):375390 Status and Distribution of Fish in an Acid-impacted  

E-Print Network [OSTI]

of the northeastern US. Introduction The ecological impacts of anthropogenic acidification (acid rain) on fishNORTHEASTERN NATURALIST2008 15(3):375­390 Status and Distribution of Fish in an Acid to chemical barriers that limit upstream movement during high flow in a few streams. As recovery from acid

Kraft, Clifford E.

338

Secretary Chu Announces Nearly $50 Million of Recovery Act Funding...  

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

Nearly 50 Million of Recovery Act Funding to Accelerate Deployment of Geothermal Heat Pumps Secretary Chu Announces Nearly 50 Million of Recovery Act Funding to...

339

Secretary Chu Announces Nearly $50 Million of Recovery Act Funding...  

Office of Environmental Management (EM)

50 Million of Recovery Act Funding to Accelerate Deployment of Geothermal Heat Pumps Secretary Chu Announces Nearly 50 Million of Recovery Act Funding to Accelerate Deployment of...

340

Recovery Act - Geothermal Technologies Program:Ground Source...  

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

Recovery Act - Geothermal Technologies Program:Ground Source Heat Pumps Recovery Act - Geothermal Technologies Program:Ground Source Heat Pumps A detailled description of the...

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


341

Energy Secretary Chu Announces $138 Million in Recovery Act Funding...  

Energy Savers [EERE]

38 Million in Recovery Act Funding for Environmental Cleanup in Ohio Energy Secretary Chu Announces 138 Million in Recovery Act Funding for Environmental Cleanup in Ohio March 31,...

342

Energy Secretary Chu Announces $148 million in Recovery Act Funding...  

Energy Savers [EERE]

48 million in Recovery Act Funding for Environmental Cleanup in New York Energy Secretary Chu Announces 148 million in Recovery Act Funding for Environmental Cleanup in New York...

343

Energy Secretary Chu Announces $384 Million in Recovery Act Funding...  

Energy Savers [EERE]

384 Million in Recovery Act Funding for Environmental Cleanup in New Mexico Energy Secretary Chu Announces 384 Million in Recovery Act Funding for Environmental Cleanup in New...

344

Exsolution Enhanced Oil Recovery with Concurrent CO2 Sequestration...  

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

Exsolution Enhanced Oil Recovery with Concurrent CO2 Sequestration. Exsolution Enhanced Oil Recovery with Concurrent CO2 Sequestration. Abstract: A novel EOR method using...

345

ITP Energy Intensive Processes: Improved Heat Recovery in Biomass...  

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

Improved Heat Recovery in Biomass-Fired Boilers ITP Energy Intensive Processes: Improved Heat Recovery in Biomass-Fired Boilers biomass-firedboilers.pdf More Documents &...

346

Recovery Act, Office of the Biomass Program,Funding Opportunity...  

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

Recovery Act, Office of the Biomass Program,Funding Opportunity Announcements Special Notice Recovery Act, Office of the Biomass Program,Funding Opportunity Announcements Special...

347

"Recovery Act: Training Program Development for Commercial Building...  

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

"Recovery Act: Training Program Development for Commercial Building Equipment Technicians, Building Operators, and Energy Commissioning AgentsAuditors" "Recovery Act: Training...

348

addiction recovery principles: Topics by E-print Network  

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

management, and recovery coaching helped, or are now helping, transform addiction treatment into a more person-centered, holistic, family-centered, and recovery-focused system...

349

Ab Initio Atomic Simulations of Antisite Pair Recovery in Cubic...  

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

Atomic Simulations of Antisite Pair Recovery in Cubic Silicon Carbide. Ab Initio Atomic Simulations of Antisite Pair Recovery in Cubic Silicon Carbide. Abstract: The thermal...

350

Post-Shred Materials Recovery Technology Development and Demonstration...  

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

Shred Materials Recovery Technology Development and Demonstration Post-Shred Materials Recovery Technology Development and Demonstration 2009 DOE Hydrogen Program and Vehicle...

351

Post-Shred Materials Recovery Technology Development and Demonstration...  

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

Post-Shred Materials Recovery Technology Development and Demonstration Post-Shred Materials Recovery Technology Development and Demonstration Presentation from the U.S. DOE Office...

352

Vehicle Technologies Office: Materials for Energy Recovery Systems...  

Energy Savers [EERE]

Energy Recovery Systems and Controlling Exhaust Gases Vehicle Technologies Office: Materials for Energy Recovery Systems and Controlling Exhaust Gases The typical internal...

353

Department of Energy Issues Loan Guarantee Supported by Recovery...  

Office of Environmental Management (EM)

Loan Guarantee Supported by Recovery Act for Nevada Geothermal Project Department of Energy Issues Loan Guarantee Supported by Recovery Act for Nevada Geothermal Project September...

354

Department of Energy Issues Loan Guarantee Supported by Recovery...  

Energy Savers [EERE]

Department of Energy Issues Loan Guarantee Supported by Recovery Act for Nevada Geothermal Project Department of Energy Issues Loan Guarantee Supported by Recovery Act for Nevada...

355

Mineral Recovery Creates Revenue Stream for Geothermal Energy...  

Energy Savers [EERE]

Mineral Recovery Creates Revenue Stream for Geothermal Energy Development Mineral Recovery Creates Revenue Stream for Geothermal Energy Development January 21, 2014 - 12:00am...

356

CLOSEOUT PROCEDURES FOR RECOVERY ACT GRANTS UNDER THE WEATHERIZATION...  

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

CLOSEOUT PROCEDURES FOR RECOVERY ACT GRANTS UNDER THE WEATHERIZATION ASSISTANCE PROGRAM CLOSEOUT PROCEDURES FOR RECOVERY ACT GRANTS UNDER THE WEATHERIZATION ASSISTANCE PROGRAM This...

357

Treasury, Energy Surpass $1 Billion Milestone in Recovery Act...  

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

Secretary Steven Chu hosted a group of clean energy developers and manufacturers at the White House to discuss how the American Recovery and Reinvestment Act (Recovery Act) is...

358

American Recovery and Reinvestment Act General Guidelines for...  

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

White House American Recovery and Reinvestment Act General Guidelines for Emblem and Logo Applications Page 1 American Recovery and Reinvestment Act General Guidelines for...

359

High Efficiency Microturbine with Integral Heat Recovery - Presentatio...  

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

High Efficiency Microturbine with Integral Heat Recovery - Presentation by Capstone Turbine Corporation, June 2011 High Efficiency Microturbine with Integral Heat Recovery -...

360

FOIA Frequently Requested Documents: DE-EE0002884 Recovery Act...  

Energy Savers [EERE]

FOIA Frequently Requested Documents: DE-EE0002884 Recovery Act - Integrated Algal Biorefinery (IABR) FOIA Frequently Requested Documents: DE-EE0002884 Recovery Act - Integrated...

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


361

Office of Electricity Delivery and Energy Reliability Recovery...  

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

Electricity Delivery and Energy Reliability Recovery Program Plan Office of Electricity Delivery and Energy Reliability Recovery Program Plan Microsoft Word - OE PSRP June 5 2009...

362

Recovery Act: Wind Energy Consortia between Institutions of Higher...  

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

Recovery Act: Wind Energy Consortia between Institutions of Higher Learning and Industry Recovery Act: Wind Energy Consortia between Institutions of Higher Learning and Industry A...

363

Treasury, Energy Announce More Than $2 Billion in Recovery Act...  

Energy Savers [EERE]

Recovery Act to increase US manufacturing output, improve energy efficiency, and develop alternative sources of energy." The Recovery Act created a new tax credit program by...

364

American Recovery & Reinvestment Act, ARRA, clean energy projects...  

Energy Savers [EERE]

Recovery & Reinvestment Act, ARRA, clean energy projects, energy efficiency, smart grid, alternative fuels, geothermal energy American Recovery & Reinvestment Act, ARRA, clean...

365

abnormal metabolic recovery: Topics by E-print Network  

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

simulation to optimize carbon dioxide (CO2) sequestration and enhance oil recovery (CO2-EOR) based on known 140 Key recovery in a business environment Computer Technologies...

366

advanced secondary recovery: Topics by E-print Network  

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

simulation to optimize carbon dioxide (CO2) sequestration and enhance oil recovery (CO2-EOR) based on known 116 Key recovery in a business environment Computer Technologies...

367

RECOVERY ACT -- CLEAN ENERGY COALITION MICHIGAN GREEN FLEETS...  

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

RECOVERY ACT -- CLEAN ENERGY COALITION MICHIGAN GREEN FLEETS RECOVERY ACT -- CLEAN ENERGY COALITION MICHIGAN GREEN FLEETS 2011 DOE Hydrogen and Fuel Cells Program, and Vehicle...

368

Thermoelectric Waste Heat Recovery Program for Passenger Vehicles...  

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

Thermoelectric Waste Heat Recovery Program for Passenger Vehicles Thermoelectric Waste Heat Recovery Program for Passenger Vehicles 2013 DOE Hydrogen and Fuel Cells Program and...

369

President Obama Announces Over $467 Million in Recovery Act Funding...  

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

Over 467 Million in Recovery Act Funding for Geothermal and Solar Energy Projects President Obama Announces Over 467 Million in Recovery Act Funding for Geothermal and Solar...

370

President Obama Announces Over $467 Million in Recovery Act Funding...  

Energy Savers [EERE]

Announces Over 467 Million in Recovery Act Funding for Geothermal and Solar Energy Projects President Obama Announces Over 467 Million in Recovery Act Funding for Geothermal and...

371

Cumulative Federal Payments to OE Recovery Act Recipients, through...  

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

September 30, 2014 Cumulative Federal Payments to OE Recovery Act Recipients, through September 30, 2014 Cumulative Federal Payments to OE Recovery Act Recipients, through...

372

Cumulative Federal Payments to OE Recovery Act Recipients, through...  

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

3 Cumulative Federal Payments to OE Recovery Act Recipients, through June 30, 2013 Graph of cumulative Federal Payments to OE Recovery Act Recipients, through June 30, 2013. OE...

373

Cumulative Federal Payments to OE Recovery Act Recipients, through...  

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

4 Cumulative Federal Payments to OE Recovery Act Recipients, through June 30, 2014 Cumulative Federal Payments to OE Recovery Act Recipients, through June 30, 2014. OE ARRA...

374

Secretary Chu Announces More than $57 Million in Recovery Act...  

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

57 Million in Recovery Act Funding to Advance Smart Grid Development Secretary Chu Announces More than 57 Million in Recovery Act Funding to Advance Smart Grid Development July...

375

Recovery Act Selections for Smart Grid Investment Grant Awards...  

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

Recovery Act Selections for Smart Grid Investment Grant Awards- By Category Updated July 2010 Recovery Act Selections for Smart Grid Investment Grant Awards- By Category Updated...

376

Synchrophasor Technologies and their Deployment in the Recovery...  

Energy Savers [EERE]

Synchrophasor Technologies and their Deployment in the Recovery Act Smart Grid Programs (August 2013) Synchrophasor Technologies and their Deployment in the Recovery Act Smart Grid...

377

Recovery Act Selections for Smart Grid Invesment Grant Awards...  

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

Recovery Act Selections for Smart Grid Invesment Grant Awards- By Category Updated July 2010 Recovery Act Selections for Smart Grid Invesment Grant Awards- By Category Updated July...

378

Thermoelectric Waste Heat Recovery Program for Passenger Vehicles...  

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

Waste Heat Recovery Program for Passenger Vehicles Thermoelectric Waste Heat Recovery Program for Passenger Vehicles 2012 DOE Hydrogen and Fuel Cells Program and Vehicle...

379

An Overview of Thermoelectric Waste Heat Recovery Activities...  

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

An Overview of Thermoelectric Waste Heat Recovery Activities in Europe An Overview of Thermoelectric Waste Heat Recovery Activities in Europe An overview presentation of R&D...

380

Energy Secretary Chu Announces $79 Million in Recovery Act Funding...  

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

79 Million in Recovery Act Funding for Environmental Cleanup in Kentucky Energy Secretary Chu Announces 79 Million in Recovery Act Funding for Environmental Cleanup in Kentucky...

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


381

LOW TEMPERATURE GEOTHERMAL MINERAL RECOVERY PROGRAM 02/11/2014...  

Energy Savers [EERE]

LOW TEMPERATURE GEOTHERMAL MINERAL RECOVERY PROGRAM 02112014 LOW TEMPERATURE GEOTHERMAL MINERAL RECOVERY PROGRAM 02112014 mineral-webinar.pdf More Documents & Publications LOW...

382

Dynamic Recovery in Silicate-Apatite Structures Under Irradiation...  

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

Recovery in Silicate-Apatite Structures Under Irradiation and Implications for Long-Term Immobilization of Actinides. Dynamic Recovery in Silicate-Apatite Structures Under...

383

Steelmaker Matches Recovery Act Funds to Save Energy & Reduce...  

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

and installed with DOE Recovery Act Funding. Blast Furnace Gas Recovery Boiler Provides Steam and Power at Steel Mill More Documents & Publications Capturing Waste Gas: Saves...

384

Laboratories for the 21st Century Best Practices: Energy Recovery...  

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

Laboratories for the 21st Century Best Practices: Energy Recovery in Laboratory Facilities Laboratories for the 21st Century Best Practices: Energy Recovery in Laboratory...

385

Audit Report: The Department of Energy's American Recovery and...  

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

of Energy's American Recovery and Reinvestment Act - California State Energy Program Audit Report: The Department of Energy's American Recovery and Reinvestment Act - California...

386

A combined Cyanex-923/HEH[EHP]/Dodecane solvent for recovery of transuranic elements from used nuclear fuel  

SciTech Connect (OSTI)

The separation of minor actinides from fission product lanthanides remains a primary challenge for enabling the recycle of used nuclear fuel. To minimize the complexity of materials handling, combining extractant processes has become an increasingly attractive option. Unfortunately, combined processes sometimes suffer reduced utility due to strong dipole-dipole interactions between the extractants. The results reported here describe a system based on a combination of commercially available extractants Cyanex-923 and HEH[EHP]. In contrast to other combined extractant systems, these extractant molecules exhibit comparatively weak interactions, reducing the impact of secondary interactions. In this process, mixtures containing equal ratios of Cyanex-923 and HEH[EHP] were seen to co-extract americium and the lanthanides from nitric acid solutions. Stripping of An(III) was effectively achieved through contact with an aqueous phase comprised of glycine (for pH control) and a polyamino-poly-carboxylate stripping reagent that selectively removes An(III) from the extractant phase. The lanthanides can then be stripped from the loaded organic phase contacting with high nitric acid concentrations. Extraction of fission products zirconium and molybdenum was also investigated and potential strategies for their management have been identified. The work presented demonstrates the feasibility of combining Cyanex-923 and HEH[EHP] for separating and recovering the transuranic elements from the Ln(III). (authors)

Johnson, A.; Nash, K.L. [Department of Chemistry, Washington State University, PO Box 644630, Pullman, WA 99164-4630 (United States)

2013-07-01T23:59:59.000Z

387

Hydraulic fracturing accelerates coalbed methane recovery  

SciTech Connect (OSTI)

Methane production from deep coal seams that never will be mined requires hydraulic fracturing for faster, optimal recovery. Since this can be a complex process, proper formation evaluation beforehand is essential, according to this paper.

Holditch, S.A. (Texas A and M Univ. (US)); Ely, J.W.; Semmelbeck, M.E.; Carter, R.H. (S.A. Holditch and Associates (US)); Hinkel, J.J.; Jeffrey, R.G. Jr. (Dowell Schlumberger (US))

1990-11-01T23:59:59.000Z

388

Recovery Act-Funded HVAC projects  

Broader source: Energy.gov [DOE]

The U.S. Department of Energy was allocated funding from the American Recovery and Reinvestment Act to conduct research into heating, ventilation, and air conditioning (HVAC) technologies and...

389

Autonomous thruster failure recovery for underactuated spacecraft  

E-Print Network [OSTI]

Thruster failures historically account for a large percentage of failures that have occurred on orbit. Therefore, autonomous thruster failure detection, isolation, and recovery (FDIR) is an essential component to any robust ...

Pong, Christopher Masaru

2010-01-01T23:59:59.000Z

390

RECOVERY ACT: TAPOCO PROJECT: CHEOAH UPGRADE  

SciTech Connect (OSTI)

Under Funding Opportunity Announcement Number: DE-FOA-0000120, Recovery Act: Hydroelectric Facility Modernization, Alcoa Power Generating Inc. (APGI), a fully owned subsidiary of Alcoa Inc., implemented major upgrades at its Cheoah hydroelectric facility near Robbinsville, North Carolina.

Paul Tran; 293 Highway 740; Baden, NC 28009

2013-02-28T23:59:59.000Z

391

Use Feedwater Economizers for Waste Heat Recovery  

SciTech Connect (OSTI)

This revised ITP tip sheet on feedwater economizers for waste heat recovery provides how-to advice for improving industrial steam systems using low-cost, proven practices and technologies.

Not Available

2006-01-01T23:59:59.000Z

392

Industrial Heat Recovery with Organic Rankine Cycles  

E-Print Network [OSTI]

Rising energy costs are encouraging energy intensive industries to investigate alternative means of waste heat recovery from process streams. The use of organic fluids in Rankine cycles offers improved potential for economical cogeneration from...

Hnat, J. G.; Patten, J. S.; Cutting, J. C.; Bartone, L. M.

1982-01-01T23:59:59.000Z

393

Recovery Act-Funded Working Fluid Projects  

Broader source: Energy.gov [DOE]

The U.S. Department of Energy was allocated funding from the American Recovery and Reinvestment Act to conduct research into working fluid technologies and applications. Projects funded by the...

394

Autonomous Thruster Failure Recovery for Underactuated Spacecraft  

E-Print Network [OSTI]

. Miller September 2010 SSL #13­10 #12;2 #12;Autonomous Thruster Failure Recovery for Underactuated Spacecraft Christopher Masaru Pong, David W. Miller September 2010 SSL #12­11 This work is based

395

Gravity Recovery and Interior Laboratory (GRAIL) Launch  

E-Print Network [OSTI]

Gravity Recovery and Interior Laboratory (GRAIL) Launch Press Kit/AUGUst 2011 #12;http of its four channels to AC-3, making each channel's secondary audio MPEG 1 Layer II. For digital downlink

396

Pennsylvania Solid Waste- Resource Recovery Development Act  

Broader source: Energy.gov [DOE]

This act promotes the construction and the application of solid waste disposal/processing and resource recovery systems that preserve and enhance the quality of air, water, and land resources. The...

397

Heat Recovery Design Considerations for Cogeneration Systems  

E-Print Network [OSTI]

The design and integration of the heat recovery section, which includes the steam generation, auxiliary firing, and steam turbine modules, is critical to the overall performance and economics of cogeneration, systems. In gas turbine topping...

Pasquinelli, D. M.; Burns, E. D.

398

Recovery Act-Funded Water Heating Projects  

Broader source: Energy.gov [DOE]

The U.S. Department of Energy was allocated funding from the American Recovery and Reinvestment Act to conduct research into water heating technologies and applications. Projects funded by the...

399

Recovery Act Worker Update: Mike Gunnels  

SciTech Connect (OSTI)

Mike Gunnels at the Savannah River Site tells how the Recovery Act got him out of unemployment and the benefits of training and teamwork in his new job with the Department of Energy.

Tire, Brian

2010-01-01T23:59:59.000Z

400

Energy Recovery from Potato Chip Fryers  

E-Print Network [OSTI]

The design, operating characteristics, and energy savings from an energy recovery system employed on a potato chip fryer which became operational in December, 1979, is discussed. The design incorporates a modification to an odor control system which...

McKee, H. B.; Kympton, H. W.; Arnold, J. W.; Paisan, J. J.

1980-01-01T23:59:59.000Z

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


401

An Introduction to Waste Heat Recovery  

E-Print Network [OSTI]

our dependence on petroleum-based fuels, paper, glass, and agricultural and automotive and hence improve our merchandise .trade balance. equipment industries have all had proven success with heat recovery projects. Solar, wind, geothermal, oil shale...

Darby, D. F.

402

Catastrophic Incident Recovery: Long-Term Recovery from an Anthrax Event Symposium  

SciTech Connect (OSTI)

On March 19, 2008, policy makers, emergency managers, and medical and Public Health officials convened in Seattle, Washington, for a workshop on Catastrophic Incident Recovery: Long-Term Recovery from an Anthrax Event. The day-long symposium was aimed at generating a dialogue about restoration and recovery through a discussion of the associated challenges that impact entire communities, including people, infrastructure, and critical systems.

Lesperance, Ann M.

2008-06-30T23:59:59.000Z

403

Pressure swing adsorption with intermediate product recovery  

SciTech Connect (OSTI)

A pressure swing adsorption process is used to achieve intermediate product recovery by the introduction of a gas displacement step before, simultaneous with or subsequent to pressure equalization between beds of a multi-bed adsorption system. A cocurrent depressurization step is then employed to achieve intermediate product recovery. A portion of said intermediate product or of the more readily adsorbable component recovered from a bed advantageously being employed to provide displacement gas for another bed in the adsorption system.

Fuderer, A.

1985-04-23T23:59:59.000Z

404

Modeling Dynamics of Post Disaster Recovery  

E-Print Network [OSTI]

Subject: Civil Engineering iii ABSTRACT Modeling Dynamics of Post Disaster Recovery. (August 2011) Ali Nejat, B.S., Zanjan University, Zanjan, Iran; M.S., Islamic Azad University, Tehran, Iran Chair of Advisory Committee: Dr. Ivan Damnjanovic... MODELING DYNAMICS OF POST DISASTER RECOVERY A Dissertation by ALI NEJAT Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY...

Nejat, Ali

2012-10-19T23:59:59.000Z

405

Faces of the Recovery Act: 1366 Technologies  

SciTech Connect (OSTI)

LEXINGTON, MA - At 1366 Technologies, Ely Sachs and Frank van Mierlo are using ARPA-E Recovery Act funding to dramatically reduce the costs of solar panel production. To read more about the project: http://arpa-e.energy.gov/FundedProjects.aspx#1366 To see more projects funded by the Recovery Act through ARPA-E: http://arpa-e.energy.gov/FundedProjects.aspx

Sachs, Ely; Mierlo, Frank van; Obama, Barack

2010-01-01T23:59:59.000Z

406

Exhaust Gas Energy Recovery Technology Applications  

SciTech Connect (OSTI)

Exhaust waste heat recovery systems have the potential to significantly improve vehicle fuel economy for conventional and hybrid electric powertrains spanning passenger to heavy truck applications. This chapter discusses thermodynamic considerations and three classes of energy recovery technologies which are under development for vehicle applications. More specifically, this chapter describes the state-of-the-art in exhaust WHR as well as challenges and opportunities for thermodynamic power cycles, thermoelectric devices, and turbo-compounding systems.

Wagner, Robert M [ORNL] [ORNL; Szybist, James P [ORNL] [ORNL

2014-01-01T23:59:59.000Z

407

Biochemically enhanced oil recovery and oil treatment  

SciTech Connect (OSTI)

This invention relates to the preparation of new, modified organisms, through challenge growth processes, that are viable in the extreme temperature, pressure and pH conditions and salt concentrations of an oil reservoir and that are suitable for use in microbial enhanced oil recovery. The modified microorganisms of the present invention are used to enhance oil recovery and remove sulfur compounds and metals from the crude oil.

Premuzic, Eugene T. (East Moriches, NY); Lin, Mow (Rocky Point, NY)

1994-01-01T23:59:59.000Z

408

Biochemically enhanced oil recovery and oil treatment  

DOE Patents [OSTI]

This invention relates to the preparation of new, modified organisms, through challenge growth processes, that are viable in the extreme temperature, pressure and pH conditions and salt concentrations of an oil reservoir and that are suitable for use in microbial enhanced oil recovery. The modified microorganisms of the present invention are used to enhance oil recovery and remove sulfur compounds and metals from the crude oil. 62 figures.

Premuzic, E.T.; Lin, M.

1994-03-29T23:59:59.000Z

409

Faces of the Recovery Act: 1366 Technologies  

ScienceCinema (OSTI)

LEXINGTON, MA - At 1366 Technologies, Ely Sachs and Frank van Mierlo are using ARPA-E Recovery Act funding to dramatically reduce the costs of solar panel production. To read more about the project: http://arpa-e.energy.gov/FundedProjects.aspx#1366 To see more projects funded by the Recovery Act through ARPA-E: http://arpa-e.energy.gov/FundedProjects.aspx

Sachs, Ely; Mierlo, Frank van; Obama, Barack

2013-05-29T23:59:59.000Z

410

Recovery of tritium from tritiated molecules  

DOE Patents [OSTI]

This invention relates to the recovery of tritium from various tritiated molecules by reaction with uranium. More particularly, the invention relates to the recovery of tritium from tritiated molecules by reaction with uranium wherein the reaction is conducted in a reactor which permits the reaction to occur as a moving front reaction from the point where the tritium enters the reactor charged with uranium down the reactor until the uranium is exhausted.

Swansiger, W.A.

1984-10-17T23:59:59.000Z

411

Recovery Act State Summaries | Department of Energy  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious Rank EERE: AlternativeEnvironment,Institutes and Launches theResidentialRecovery Act State Summaries Recovery

412

The role of nitric oxide in testosterone-induced vasodilation in pig coronary arteries and rat thoracic aorta  

E-Print Network [OSTI]

Several studies have provided evidence that the administration of testosterone to vascular tissue causes vasodilation (Costarella, Yue). This study examines the role of nitric oxide (NO) as a potential mechanism of testosterone-induced vasodilation...

Piefer, Jason William

2013-02-22T23:59:59.000Z

413

Specific Visualization of Nitric Oxide in the Vasculature with Two-Photon Microscopy Using a Copper Based Fluorescent Probe  

E-Print Network [OSTI]

To study the role and (sub) cellular nitric oxide (NO) constitution in various disease processes, its direct and specific detection in living cells and tissues is a major requirement. Several methods are available to measure ...

Ghosh, Mitrajit

414

Investigation on Nitric Oxide and Soot of Biodiesel and Conventional Diesel using a Medium Duty Diesel Engine  

E-Print Network [OSTI]

Biodiesel has been suggested as an alternative fuel to the petroleum diesel fuel. It beneficially reduces regulated emission gases, but increases NOx (nitric oxide and nitrogen dioxide) Thus, the increase in NOx is the barrier for potential growth...

Song, Hoseok

2012-07-16T23:59:59.000Z

415

Precious Metal Recovery from Fuel Cell MEA's  

SciTech Connect (OSTI)

One of the next-generation power sources is the proton exchange membrane (PEM) fuel cell, which runs on pure hydrogen or hydrogen-rich reformate. At the heart of the PEM fuel cell is a membrane electrode assembly (MEA). The MEA is a laminate composed of electrode layers sandwiched between outer layers, fabricated from either carbon fiber or fabric and which control the diffusion of reactant gases, and the inner polymer mebrane. Hydrogen is oxidized at the anode to form protons, which migrate through the membrane and react with oxygen at the cathode to form water. In this type of fuel cell, platinum catalyzes the reactions at both electrodes. Realization of a future that includes ubiquitous use of hydrogen fuel cell-powered vehicles will be partially contingent on a process for recycling components of the fuel cell membrane electrode assemblies. In aggregate, the platinum used for the fuel cell will represent a large pool of this precious metal, and the efficient recycling of Pt from MEA's will be a cost-enabling factor for success of this technology. Care must be taken in the reclamation process because of the presence of fluoropolymers in the MEA. While Pt is normally recovered with high yield, the combustion process commonly applied to remove an organic matrix will also liberate a large volume of HF, a gas which is both toxic and corrosive. Carbonyl fluoride, which has a recommended exposure limit of 2ppmv, is another undesirable product of fluoroploymer combustion. In 2003, the Department of Energy awarded Engelhard Corporation an 80% cost share grant for a five-year project budgeted at $5.9MM. The principal objective is reclaiming platinum from fuel cell MEA's without producing fluorine-containing emissions. Over the last three years, Engelhard has approached the problem from several directions in balancing the two goals: a commercially-viable recycling process and an environmentally favorable one. Working with both fresh and aged fuel cells, it has been shown that precious metals can be liberated at high yield using microwave assisted acid digestion, but exposure of the gas diffusion electrode surfaces is required. A low-cost solvent-stripping process has been identified for two geometries of fuel cell MEA's: GDL and GDE. This paper will detail progress made in realizing a practical, "green" process for recovery of Pt from PEM fuel cell MEA's

Lawrence Shore

2006-11-16T23:59:59.000Z

416

LOWER COLUMBIA SALMON RECOVERY & SUBBASIN PLAN December 2004 RECOVERY GOALS 5-1  

E-Print Network [OSTI]

." This vision for recovery encompasses ESA de-listing goals in the sense that ESA de-listing could be achieved

417

Demonstration of a TODGA/TBP process for recovery of trivalent actinides and lanthanides from a PUREX raffinate  

SciTech Connect (OSTI)

The efficiency of the partitioning of trivalent actinides from a PUREX raffinate has been demonstrated with a TODGA + TBP extractant mixture dissolved in an industrial aliphatic solvent TPH. Based on the results coming from cold and hot batch extraction studies and with the aid of computer code calculations a continuous counter current process have been developed and two flowsheets were tested using miniature centrifugal contactors. The feed solutions was a synthetic PUREX raffinate, spiked with {sup 241}Am, {sup 244}Cm, {sup 252}Cf, {sup 152}Eu and {sup 134}Cs. More than 99.9 % of the trivalent actinides and lanthanides were extracted and back-extracted and very high decontamination factors to most fission products were obtained. Co-extraction of zirconium, molybdenum and palladium was prevented using oxalic acid and HEDTA. However 10% of ruthenium was extracted and only 3 % could be back extracted using diluted nitric acid. (authors)

Modolo, G.; Asp, H.; Vijgen, H. [Forschungszentrum Juelich GmbH, Institut fuer Energieforschung, 52425 Juelich (Germany); Malmbeck, R.; Magnusson, D. [European Commission, JRC, Institute for Transuranium Elements - ITU, 76125 Karlsruhe (Germany); Sorel, C. [Commissariat a l'Energie Atomique Valrho - CEA, DRCP/SCPS, BP17171, 30207 Bagnols-sur-Ceze (France)

2007-07-01T23:59:59.000Z

418

BNL Citric Acid Technology: Pilot Scale Demonstration  

SciTech Connect (OSTI)

The objective of this project is to remove toxic metals such as lead and cadmium from incinerator ash using the Citric Acid Process developed at Brookhaven National Laboratory. In this process toxic metals in bottom ash from the incineration of municipal solid waste were first extracted with citric acid followed by biodegradation of the citric acid-metal extract by the bacterium Pseudomonas fluorescens for metals recovery. The ash contained the following metals: Al, As, Ba, Ca, Cd, Cr, Cu, Fe, Mg, Mn, Ni, Pb, Se, Sr, Ti, and Zn. Optimization of the Citric Acid Process parameters which included citric acid molarity, contact time, the impact of mixing aggressiveness during extraction and pretreatment showed lead and cadmium removal from incinerator ash of >90%. Seeding the treated ash with P. fluorescens resulted in the removal of residual citric acid and biostabilization of any leachable lead, thus allowing it to pass EPA?s Toxicity Characteristic Leaching Procedure. Biodegradation of the citric acid extract removed >99% of the lead from the extract as well as other metals such as Al, Ca, Cu, Fe, Mg, Mn, Ti, and Zn. Speciation of the bioprecipitated lead by Extended X-ray Absorption Fine Structure at the National Synchrotron Light Source showed that the lead is predominantly associated with the phosphate and carboxyl functional groups in a stable form. Citric acid was completely recovered (>99%) from the extract by sulfide precipitation technique and the extraction efficiency of recovered citric acid is similar to that of the fresh citric acid. Recycling of the citric acid should result in considerable savings in the overall treatment cost. We have shown the potential application of this technology to remove and recover the metal contaminants from incinerator ash as well as from other heavy metal bearing wastes (i.e., electric arc furnace dust from steel industry) or soils. Information developed from this project is being applied to demonstrate the remediation of lead paint contaminated soils on Long Island.

FRANCIS, A J; DODGE,; J, C; GILLOW, J B; FORRESTER, K E

1999-09-24T23:59:59.000Z

419

Improved method for extracting lanthanides and actinides from acid solutions  

DOE Patents [OSTI]

A process for the recovery of actinide and lanthanide values from aqueous acidic solutions uses a new series of neutral bi-functional extractants, the alkyl(phenyl)-N,N-dialkylcarbamoylmethylphosphine oxides. The process is suitable for the separation of actinide and lanthanide values from fission product values found together in high-level nuclear reprocessing waste solutions.

Horwitz, E.P.; Kalina, D.G.; Kaplan, L.; Mason, G.W.

1983-07-26T23:59:59.000Z

420

Evaluate Supply and Recovery of Woody Biomass for Energy  

E-Print Network [OSTI]

Biomass Recovery DataContrasting Woody Biomass Recovery Data Forest Biomass Supply in the Southeastern4/11/2011 1 Evaluate Supply and Recovery of Woody Biomass for Energy Production from Natural. Other studies of biomass supply have supply have assumedassumed a technical recovery rate

Gray, Matthew

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


421

Measurement of Nitric Oxide Production from Lymphatic Entothelial Cells Under Mechanical Stimuli  

E-Print Network [OSTI]

MEASUREMENT OF NITRIC OXIDE PRODUCTION FROM LYMPHATIC ENDOTHELIAL CELLS UNDER MECHANICAL STIMULI A Thesis by MOHAMMAD JAFARNEJAD Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment... Engineering Copyright 2012 Mohammad Jafarnejad ii ABSTRACT The lymphatic system plays an important role in fluid and protein balance within the interstitial spaces. Its dysfunction could result in a number of debilitating diseases, namely...

Jafarnejad, Mohammad 1987-

2012-11-16T23:59:59.000Z

422

Complexation of lanthanides and actinides by acetohydroxamic acid  

SciTech Connect (OSTI)

Acetohydroxamic acid (AHA) has been proposed as a suitable reagent for the complexant-based, as opposed to reductive, stripping of plutonium and neptunium ions from the tributylphosphate solvent phase in advanced PUREX or UREX processes designed for future nuclear-fuel reprocessing. Stripping is achieved by the formation of strong hydrophilic complexes with the tetravalent actinides in nitric acid solutions. To underpin such applications, knowledge of the complexation constants of AHA with all relevant actinide (5f) and lanthanide (4f) ions is therefore important. This paper reports the determination of stability constants of AHA with the heavier lanthanide ions (Dy-Yb) and also U(IV) and Th(IV) ions. Comparisons with our previously published AHA stability-constant data for 4f and 5f ions are made. (authors)

Taylor, R.J. [British Technology Centre, Nexia Solutions, Sellafield, Seascale, CA20 1PG (United Kingdom); Sinkov, S.I. [Pacific Northwest National Laboratory, Richland, WA 99352 (United States); Choppin, G.R. [Department of Chemistry and Biochemistry, Florida State University, Tallahassee, FL (United States)

2008-07-01T23:59:59.000Z

423

Resource Recovery Opportunities at America’s Water Resource Recovery Facilities  

Broader source: Energy.gov [DOE]

Breakout Session 3A—Conversion Technologies III: Energy from Our Waste—Will we Be Rich in Fuel or Knee Deep in Trash by 2025? Resource Recovery Opportunities at America’s Water Resource Recovery Facilities Todd Williams, Deputy Leader for Wastewater Infrastructure Practice, CH2M HILL

424

PLUTONIUM-238 RECOVERY FROM IRRADIATED NEPTUNIUM TARGETS USING SOLVENT EXTRACTION  

SciTech Connect (OSTI)

The United States Department of Energy proposes to re-establish a domestic capability for producing plutonium-238 (238Pu) to fuel radioisotope power systems primarily in support of future space missions. A conceptual design report is currently being prepared for a new 238Pu, and neptunium-237 (237Np) target fabrication and processing facility tentatively to be built at the Idaho National Laboratory (INL) in the USA. The facility would be capable of producing at least 5 kg of 238Pu-oxide powder per year. Production of 238Pu requires fabrication of 237Np targets with subsequent irradiation in the existing Advanced Test Reactor (ATR) located at the INL. The targets are 237Np oxide dispersed in a compact of powdered aluminum and clad with aluminum metal. The 238Pu product is separated and purified from the residual 237Np, aluminum matrix, and fission products. The unconverted 237Np is also a valuable starting material and is separated, purified and recycled to the target fabrication process. The proposed baseline method for separating and purifying 238Pu and unconverted 237Np post irradiation is by anion exchange (IX). Separation of Pu from Np by IX was chosen as the baseline method because of the method’s proven ability to produce a quality Pu product and because it is amenable to the relatively small scale, batch type production methods used (small batches of ~200g 238Pu are processed at a time). Multiple IX cycles are required involving substantial volumes of nitric acid and other process solutions which must be cleaned and recycled or disposed of as waste. Acid recycle requires rather large evaporator systems, including one contained in a hot cell for remote operation. Finally, the organic based anion exchange resins are rapidly degraded due to the high a-dose and associated heat production from 238Pu decay, and must be regularly replaced (and disposed of as waste). In summary, IX is time consuming, cumbersome, and requires substantial tankage to accommodate the process. The primary purpose of the preliminary study discussed here is to develop an alternative process flowsheet using well-known solvent extraction (SX) techniques based on decades of experience with PUREX processing of nuclear materials. Ultimately, this initial study will be used to determine if an SX approach would offer any significant processing advantages relative to the currently proposed anion exchange process.

Scott Herbst; Terry Todd; Jack Law; Bruce Mincher; Steve Frank; John Swanson

2006-10-01T23:59:59.000Z

425

Wettability and Oil Recovery by Imbibition and Viscous Displacement from Fractured and Heterogeneous Carbonates  

SciTech Connect (OSTI)

About one-half of U.S. oil reserves are held in carbonate formations. The remaining oil in carbonate reservoirs is regarded as the major domestic target for improved oil recovery. Carbonate reservoirs are often fractured and have great complexity even at the core scale. Formation evaluation and prediction is often subject to great uncertainty. This study addresses quantification of crude oil/brine/rock interactions and the impact of reservoir heterogeneity on oil recovery by spontaneous imbibition and viscous displacement from pore to field scale. Wettability-alteration characteristics of crude oils were measured at calcite and dolomite surfaces and related to the properties of the crude oils through asphaltene content, acid and base numbers, and refractive index. Oil recovery was investigated for a selection of limestones and dolomites that cover over three orders of magnitude in permeability and a factor of four variation in porosity. Wettability control was achieved by adsorption from crude oils obtained from producing carbonate reservoirs. The induced wettability states were compared with those measured for reservoir cores. The prepared cores were used to investigate oil recovery by spontaneous imbibition and viscous displacement. The results of imbibition tests were used in wettability characterization and to develop mass transfer functions for application in reservoir simulation of fractured carbonates. Studies of viscous displacement in carbonates focused on the unexpected but repeatedly observed sensitivity of oil recovery to injection rate. The main variables were pore structure, mobility ratio, and wettability. The potential for improved oil recovery from rate-sensitive carbonate reservoirs by increased injection pressure, increased injectivity, decreased well spacing or reduction of interfacial tension was evaluated.

Norman R. Morrow; Jill Buckley

2006-04-01T23:59:59.000Z

426

Inherently safe in situ uranium recovery  

DOE Patents [OSTI]

An in situ recovery of uranium operation involves circulating reactive fluids through an underground uranium deposit. These fluids contain chemicals that dissolve the uranium ore. Uranium is recovered from the fluids after they are pumped back to the surface. Chemicals used to accomplish this include complexing agents that are organic, readily degradable, and/or have a predictable lifetime in an aquifer. Efficiency is increased through development of organic agents targeted to complexing tetravalent uranium rather than hexavalent uranium. The operation provides for in situ immobilization of some oxy-anion pollutants under oxidizing conditions as well as reducing conditions. The operation also artificially reestablishes reducing conditions on the aquifer after uranium recovery is completed. With the ability to have the impacted aquifer reliably remediated, the uranium recovery operation can be considered inherently safe.

Krumhansl, James L; Brady, Patrick V

2014-04-29T23:59:59.000Z

427

Alternate Materials for Recovery Boiler Superheater Tubes  

SciTech Connect (OSTI)

The ever escalating demands for increased efficiency of all types of boilers would most sensibly be realized by an increase in the steam parameters of temperature and pressure. However, materials and corrosion limitations in the steam generating components, particularly the superheater tubes, present major obstacles to boiler designers in achieving systems that can operate under the more severe conditions. This paper will address the issues associated with superheater tube selection for many types of boilers; particularly chemical recovery boilers, but also addressing the similarities in issues for biomass and coal fired boilers. It will also review our recent study of materials for recovery boiler superheaters. Additional, more extensive studies, both laboratory and field, are needed to gain a better understanding of the variables that affect superheater tube corrosion and to better determine the best means to control this corrosion to ultimately permit operation of recovery boilers at higher temperatures and pressures.

Keiser, James R [ORNL; Kish, Joseph [McMaster University; Singbeil, Douglas [FPInnovations

2009-01-01T23:59:59.000Z

428

User data package for implementation of electrolytic recovery technology in Navy electroplating shops. Final report, March 1993-January 1995  

SciTech Connect (OSTI)

In FY94 the Naval Facilities Engineering Service Center (NFESC) completed tests on three electrolytic recovery systems used for the recovery of metals and destruction of cyanide from electroplating wastewaters. Field testing and evaluation was conducted at NSY Norfolk, NAWC Indianapolis, and NADEP Cherry Pt. for five metal recovery applications: silver cyanide, copper cyanide, acid copper, electroless nickel, and tin-lead fluoborate. Advanced design features for metal recovery, including enhanced fluidized circulation, specialized oxidizing anodes, and high porous surface area cathodes were evaluated to optimize performance. NFESC demonstrated that electrolytic recovery systems can be adapted for effective use in the Navy plating operations where production is often sporadic as contrasted to industrial plating processes. The electrolytic recovery units removed metal ions from the rinsewater to below 1 ppm for each application. Electrowinning, as an alternative technology, can reduce industrial waste treatment costs and hazardous sludge generated from conventional treatment This User Data Package (UDP) covers the design, operational and maintenance requirements for these electrolytic systems. This UDP will be applicable to small Navy plating shops where closed-loop waste recycling and point source minimization is necessary for environmental compliance and cost competitiveness.

Ford, K.; Koff, J.

1995-10-01T23:59:59.000Z

429

Extraction of Plutonium into 30 Percent Tri-Butyl Phosphate from Nitric Acid Solution Containing Fluoride, Aluminum, and Boron  

SciTech Connect (OSTI)

This work consists of experimental batch extraction data for plutonium into 30 volume-percent tri-butyl phosphate at ambient temperature from such a solution matrix and a model of this data using complexation constants from the literature.

Kyser, E.A.

2000-01-06T23:59:59.000Z

430

Recovery of lithium and cobalt from waste lithium ion batteries of mobile phone  

SciTech Connect (OSTI)

Graphical abstract: Recovery of valuable metals from scrap batteries of mobile phone. - Highlights: • Recovery of Co and Li from spent LIBs was performed by hydrometallurgical route. • Under the optimum condition, 99.1% of lithium and 70.0% of cobalt were leached. • The mechanism of the dissolution of lithium and cobalt was studied. • Activation energy for lithium and cobalt were found to be 32.4 kJ/mol and 59.81 kJ/mol, respectively. • After metal recovery, residue was washed before disposal to the environment. - Abstract: In view of the stringent environmental regulations, availability of limited natural resources and ever increasing need of alternative energy critical elements, an environmental eco-friendly leaching process is reported for the recovery of lithium and cobalt from the cathode active materials of spent lithium-ion batteries of mobile phones. The experiments were carried out to optimize the process parameters for the recovery of lithium and cobalt by varying the concentration of leachant, pulp density, reductant volume and temperature. Leaching with 2 M sulfuric acid with the addition of 5% H{sub 2}O{sub 2} (v/v) at a pulp density of 100 g/L and 75 °C resulted in the recovery of 99.1% lithium and 70.0% cobalt in 60 min. H{sub 2}O{sub 2} in sulfuric acid solution acts as an effective reducing agent, which enhance the percentage leaching of metals. Leaching kinetics of lithium in sulfuric acid fitted well to the chemical controlled reaction model i.e. 1 ? (1 ? X){sup 1/3} = k{sub c}t. Leaching kinetics of cobalt fitted well to the model ‘ash diffusion control dense constant sizes spherical particles’ i.e. 1 ? 3(1 ? X){sup 2/3} + 2(1 ? X) = k{sub c}t. Metals could subsequently be separated selectively from the leach liquor by solvent extraction process to produce their salts by crystallization process from the purified solution.

Jha, Manis Kumar, E-mail: mkjha@nmlindia.org; Kumari, Anjan; Jha, Amrita Kumari; Kumar, Vinay; Hait, Jhumki; Pandey, Banshi Dhar

2013-09-15T23:59:59.000Z

431

IOWA RECOVERY ACT SNAPSHOT | Department of Energy  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious Rank EERE:YearRound-UpHeatMulti-Dimensionalthe U.S. Department ofIOWA RECOVERY ACT SNAPSHOT IOWA RECOVERY ACT

432

Los Alamos plants willows for flood recovery  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsrucLas Conchas recovery challenge fund Las Conchas recoveryNuclearPhysicist honored byplants

433

Chemical trends at lakes ans streams in the UK Acid Waters Monitoring Network, 19882000 Hydrology and Earth System Sciences, 5(3), 351366 (2001) EGS  

E-Print Network [OSTI]

of `acid rain' were first documented in the Pennines, Northern England, following the onsetChemical trends at lakes ans streams in the UK Acid Waters Monitoring Network, 1988­2000 351 in the UK Acid Waters Monitoring Network, 1988-2000: Evidence for recent recovery at a national scale C

Paris-Sud XI, Université de

434

Water-enhanced solubility of carboxylic acids in organic solvents and its applications to extraction processes  

SciTech Connect (OSTI)

The solubilities of carboxylic acids in certain organic solvents increase remarkably with an increasing amount of water in the organic phase. This phenomenon leads to a novel extract regeneration process in which the co-extracted water is selectively removed from an extract, and the carboxylic acid precipitates. This approach is potentially advantageous compared to other regeneration processes because it removes a minor component of the extract in order to achieve a large recovery of acid from the extract. Carboxylic acids of interest include adipic acid, fumaric acid, and succinic acid because of their low to moderate solubilities in organic solvents. Solvents were screened for an increase in acid solubility with increased water concentration in the organic phase. Most Lewis-base solvents were found to exhibit this increased solubility phenomena. Solvents that have a carbonyl functional group showed a very large increase in acid solubility. 71 refs., 52 figs., 38 tabs.

Starr, J.N.; King, C.J.

1991-11-01T23:59:59.000Z

435

Software Update Recovery for Wireless Sensor Networks  

E-Print Network [OSTI]

mechanism that uses loss-of- control to provide high-reliability, low energy, software updates, includingSoftware Update Recovery for Wireless Sensor Networks Stephen Brown1 and Cormac J. Sreenan2 1 Laboratory, University College Cork, Ireland Abstract. Updating software over the network is important

Sreenan, Cormac J.

436

Rankine cycle waste heat recovery system  

DOE Patents [OSTI]

This disclosure relates to a waste heat recovery (WHR) system and to a system and method for regulation of a fluid inventory in a condenser and a receiver of a Rankine cycle WHR system. Such regulation includes the ability to regulate the pressure in a WHR system to control cavitation and energy conversion.

Ernst, Timothy C.; Nelson, Christopher R.

2014-08-12T23:59:59.000Z

437

Remediation and Recovery of Uranium from Contaminated  

E-Print Network [OSTI]

Remediation and Recovery of Uranium from Contaminated Subsurface Environments with Electrodes K E L that Geobacter species can effectively remove uranium from contaminated groundwater by reducing soluble U was stably precipitated until reoxidized in the presence of oxygen. When an electrode was placed in uranium

Lovley, Derek

438

Recovery Act Weekly Video: 200 West Drilling  

ScienceCinema (OSTI)

President of Cascade Drilling, Bruce, talks about his contract with the Department of Energy and what his team is doing to improve water treatment and environmental cleanup. The small business owner hits on how the Recovery Act saved him from downsizing and helped him stay competitive and safe on site.

None

2012-06-14T23:59:59.000Z

439

Fluid Catalytic Cracking Power Recovery Computer Simulation  

E-Print Network [OSTI]

re covery available in new plants results in the air string being almost self sustaining, 8S far as direct input power. With some processes, it is possible to produce excess power on the order of 1,000 to 9,000 HP. Waste heat recovery in the form...

Samurin, N. A.

1979-01-01T23:59:59.000Z

440

PREDICTIVE MODELS. Enhanced Oil Recovery Model  

SciTech Connect (OSTI)

PREDICTIVE MODELS is a collection of five models - CFPM, CO2PM, ICPM, PFPM, and SFPM - used in the 1982-1984 National Petroleum Council study of enhanced oil recovery (EOR) potential. Each pertains to a specific EOR process designed to squeeze additional oil from aging or spent oil fields. The processes are: 1 chemical flooding; 2 carbon dioxide miscible flooding; 3 in-situ combustion; 4 polymer flooding; and 5 steamflood. CFPM, the Chemical Flood Predictive Model, models micellar (surfactant)-polymer floods in reservoirs, which have been previously waterflooded to residual oil saturation. Thus, only true tertiary floods are considered. An option allows a rough estimate of oil recovery by caustic or caustic-polymer processes. CO2PM, the Carbon Dioxide miscible flooding Predictive Model, is applicable to both secondary (mobile oil) and tertiary (residual oil) floods, and to either continuous CO2 injection or water-alternating gas processes. ICPM, the In-situ Combustion Predictive Model, computes the recovery and profitability of an in-situ combustion project from generalized performance predictive algorithms. PFPM, the Polymer Flood Predictive Model, is switch-selectable for either polymer or waterflooding, and an option allows the calculation of the incremental oil recovery and economics of polymer relative to waterflooding. SFPM, the Steamflood Predictive Model, is applicable to the steam drive process, but not to cyclic steam injection (steam soak) processes. The IBM PC/AT version includes a plotting capability to produces a graphic picture of the predictive model results.

Ray, R.M. [DOE Bartlesville Energy Technology Center, Bartlesville, OK (United States)

1992-02-26T23:59:59.000Z

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


441

Disaster Resiliency and Recovery: Capabilities (Fact Sheet)  

SciTech Connect (OSTI)

The National Renewable Energy Laboratory (NREL) is the nation's leader in energy efficient and renewable energy technologies, practices, and strategies. For the last 15 years, NREL has provided expertise, tools, and innovations to private industry; federal, state, and local governments; non-profit organizations; and communities during the planning, recovery, and rebuilding stages after disaster strikes.

Not Available

2012-11-01T23:59:59.000Z

442

The Economic Recovery Tax Act of 1981.  

E-Print Network [OSTI]

The Texas A&M University System Texas Agricultural Extension Service Zerle L. Carpenter, Director College Station B-1456 The Economic Recovery Tax Act of 1981 Better Estate Plannin CONTENTS Increase in Unified Credit... .................................................................... 7 Repeal of Orphans' Exclusion ............................................................. 7 Delay in the Imposition of New Generation-Skipping Tax .................................... 7 Technical Changes in Special Use Valuation Provisions...

Pena, Jose G.; Lovell, Ashley C.; Kensing, Robert H.

1983-01-01T23:59:59.000Z

443

Asynchronous intrusion recovery for interconnected web services  

E-Print Network [OSTI]

Asynchronous intrusion recovery for interconnected web services Ramesh Chandra, Taesoo Kim, and tracking down and recovering from such an attack re- quires significant manual effort. Web services for such web services. Aire addresses several challenges, such as propagating repair across services when some

Sabatini, David M.

444

Heat Recovery Boilers for Process Applications  

E-Print Network [OSTI]

of the use of heat recovery due primarily to process considerations. On the other hand, cost and payback are main considerations in the case of gas turbine and incineration plants, where large quantities of gases are exhausted at temperatures varying from 800...

Ganapathy, V.; Rentz, J.; Flanagan, D.

445

California's Energy Recovery and Reinvestment Act  

E-Print Network [OSTI]

efficiency measures - $25 million · Green Job Workforce - $20 millionGreen Job Workforce $20 million · EnergyCalifornia's Energy Recovery and Reinvestment Act P I iti tiProgram Initiatives November 18, 2009 Director Economic Stimulus Program California Energy CommissionCalifornia Energy Commission #12

446

Managing Manure with Biogas Recovery Systems  

E-Print Network [OSTI]

such as natural gas, propane, and fuel oil. Biogas can also be flared to control odor if energy recovery: a digester, a gas-handling system, a gas-use device, and a manure storage tank or pond to hold the treat- ed.g., storage tanks, storage ponds, lagoons). These benefits include odor control, improved air and water

Mukhtar, Saqib

447

Asset Management Equipment Disposal Form -Refrigerant Recovery  

E-Print Network [OSTI]

enters the waste stream with the charge intact (e.g., motor vehicle air conditioners, refrigeratorsAsset Management Equipment Disposal Form - Refrigerant Recovery Safe Disposal Requirements Under refrigeration, cold storage warehouse refrigeration, chillers, and industrial process refrigeration) has to have

Sin, Peter

448

An Integrated Low Level Heat Recovery System  

E-Print Network [OSTI]

A large amount of low level thermal energy is lost to air or water in a typical petroleum refinery. This paper discusses a complex integrated low level heat recovery system that is being engineered for installation in a large petroleum refinery...

Sierra, A. V., Jr.

1981-01-01T23:59:59.000Z

449

Waste water treatment and metal recovery  

E-Print Network [OSTI]

Waste water treatment and metal recovery Nickel catalysts for hydrogen production Nickel and single versions of which contained cobalt, chromium, carbon, molybdenum, tungsten, and nickel. In 1911 and 1912% on their stainless steel production. The company paid sizable dividends to its owners until it was dissolved

Braun, Paul

450

Avoided Gigawatts Through Utility Capital Recovery Fees  

E-Print Network [OSTI]

structure is possible through the use of capital recovery fees for new electric meter hookups similar to those commonly used for new water and wastewater hookups where the developer/owner is required to capitalize the marginal cost of new demand. By giving...

Frosenfeld, A. N.; Verdict, M. E.

1985-01-01T23:59:59.000Z

451

Methane Digesters and Biogas Recovery - Masking the Environmental Consequences of Industrial Concentrated Livestock Production  

E-Print Network [OSTI]

DIGESTERS AND BIOGAS RECOVERY Digesters Do Not Address theMethane Digesters and Biogas Recovery-Masking theII. METHANE DIGESTERS AND BIOGAs RECOVERY- IN THE

Di Camillo, Nicole G.

2011-01-01T23:59:59.000Z

452

E-Print Network 3.0 - additional reserve recovery Sample Search...  

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

recovery Summary: , measuring the recovery of congeners of polychlorinated dibenzo-p-dioxins (PCDDs). In addition, we measured... and showed satisfactory recoveries of all of the...

453

Methane Digesters and Biogas Recovery - Masking the Environmental Consequences of Industrial Concentrated Livestock Production  

E-Print Network [OSTI]

Methane Digesters and Biogas Recovery-Masking theII. METHANE DIGESTERS AND BIOGAs RECOVERY- IN THE2011] METHANE DIGESTERS AND BIOGAS RECOVERY methane, and 64%

Di Camillo, Nicole G.

2011-01-01T23:59:59.000Z

454

Extracting metal ions with diphosphonic acid, or derivative thereof  

DOE Patents [OSTI]

Thermodynamically-unstable complexing agents which are diphosphonic acids and diphosphonic acid derivatives (or sulfur containing analogs), like carboxyhydroxymethanediphosphonic acid and vinylidene-1,1-diphosphonic acid, are capable of complexing with metal ions, and especially metal ions in the II, III, IV, V and VI oxidation states, to form stable, water-soluble metal ion complexes in moderately alkaline to highly-acidic media. However, the complexing agents can be decomposed, under mild conditions, into non-organic compounds which, for many purposes are environmentally-nondamaging compounds thereby degrading the complex and releasing the metal ion for disposal or recovery. Uses for such complexing agents as well as methods for their manufacture are also described. 1 fig.

Horwitz, E.P.; Gatrone, R.C.; Nash, K.L.

1994-07-26T23:59:59.000Z

455

Selective reduction of nitric oxide with ammonia over vanadia on pillared titanium phosphate  

E-Print Network [OSTI]

in the catalyst. Shikada et al. (1981) compared AlzOz, SiOz, and SiO, ? TiOz (equimolar) supports for VzOs using a simulated flue gas containing 100 ppni SOz. The silica- titanium dioxide supported catalyst showed the highest NO conversions followed by those...SELECTIVE REDUCTION OF NITRIC OXIDE YVITH AMMONIA OVER VANADIA ON PILLARED TITANIUM PHOSPHATE A Thesis LAWRENCE JOSEPH CZARNECKI Submitted to the Graduate College of Texas AkM University in partial fulfillment of the requirement for the degree...

Czarnecki, Lawrence Joseph

1988-01-01T23:59:59.000Z

456

The selective catalytic reduction of nitric oxide with ammonia in the presence of oxygen  

E-Print Network [OSTI]

supporting the authors conclusions. Kato, et al. (1981 a) studied the catalytic activity of' iron oxide-titanium oxide catalysts with Fe/Ti atonuc ratios of 1/9 for the NO ? NHs ? Oz reaction. No NqO ivas detected in the reaction products, regardless... of the fact that an excess of oxygen ivas present in each reaction stuay. Nitric oxide and ammonia reacted stoichiometrically, regardless of the oxygen concentration, the space velocity, the temperature or the presence of SOz and HqO. The rate...

Gruber, Karen Ann

1989-01-01T23:59:59.000Z

457

Sampling, preservation, and analytical methods research plan - liquid redox sulfur recovery technologies: Stretford process. Topical report  

SciTech Connect (OSTI)

GRI has developed a sampling, preservation, and analytical (SPandA) methods research plan for developing and validating analytical methodologies for liquid redox sulfur recovery processes (e.g., Stretford process). The document describes the technical approach which will be used to direct research activities to develop SPandA methodologies to analyze gaseous, aqueous, and solid process streams from the Stretford sulfur recovery process. The primary emphasis is on developing and validating methodologies for analyzing vanadium (IV) and vanadium (V), anthraquinone disulphonic acids (ADA), polysulfide-sulfur, sulfide-sulfur, thiosulfate, sulfate, thiocyanate, total soluble sulfur, alkalinity, pH, total dissolved solids, total suspended solids, and dissolved oxygen in aqueous process streams. The document includes descriptions of the process streams and chemical species, selection of candidate analytical methods, and technical approach for methods development and validation.

Trofe, T.W.

1986-11-01T23:59:59.000Z

458

Recovery Act Helps Fuel Cell Company Stay on Course | Department...  

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

Recovery Act Helps Fuel Cell Company Stay on Course Recovery Act Helps Fuel Cell Company Stay on Course January 7, 2010 - 3:41pm Addthis Joshua DeLung An innovative company in...

459

BRIEF REPORT Autonomic recovery and habituation in social anxiety  

E-Print Network [OSTI]

trait socially anxious (HTSA) and low trait socially anxious (LTSA) individuals show comparable between groups might emerge during recovery or habituation, 35 HTSA and LTSA participants gave two the LTSA participants, autonomic measures showed comparable reactivity, habituation, and recovery

Gross, James J.

460

SIMULTANEOUS DEMULTIPLEXING, ELECTRICAL CLOCK RECOVERY, AND OPTICAL CLOCK GENERATION USING  

E-Print Network [OSTI]

SIMULTANEOUS DEMULTIPLEXING, ELECTRICAL CLOCK RECOVERY, AND OPTICAL CLOCK GENERATION USING of the PLL. As a result, simultaneous demultiplexing, electrical clock recovery and optical clock generation), and Masashi Usami (2) 1 : Department of Electrical and Computer Engineering, University of California Santa

Bowers, John

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


461

Energy Savings By Recovery of Condensate From Steam Heating System  

E-Print Network [OSTI]

The recovery and utilization of condensate has a remarkable energy saving effect if the following are properly done: 1) Determination of a correct and reasonable recovery plan; 2) Selection of bleed valve with good performance; 3) Solving...

Cheng, W. S.; Zhi, C. S.

462

Integration of a "Passive Water Recovery" MEA into a Portable...  

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

Integration of a "Passive Water Recovery" MEA into a Portable DMFC Power Supply Integration of a "Passive Water Recovery" MEA into a Portable DMFC Power Supply Download slides from...

463

Methane productivity and nutrient recovery from manure Henrik B. Mller  

E-Print Network [OSTI]

Methane productivity and nutrient recovery from manure Henrik B. Møller Danish Institute This thesis, entitled "Methane productivity and nutrient recovery from manure" is presented in partial of digested and separated products.................... 13 3. Methane productivity and greenhouse gas emissions

464

Industrial HVAC Air-to-Air Energy Recovery Retrofit Economics  

E-Print Network [OSTI]

Retrofitting air-to-air energy recovery equipment is relatively simply to design and easy to install. Additionally, HVAC energy recovery is almost risk free when compared to process retrofit. Life cycle cost analysis is the best way to illustrate...

Graham, E. L.

1980-01-01T23:59:59.000Z

465

SUBJECT: CALCULATION OF JOB CREATION THROUGH RECOVERY ACT FUNDING...  

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

SUBJECT: CALCULATION OF JOB CREATION THROUGH RECOVERY ACT FUNDING SUBJECT: CALCULATION OF JOB CREATION THROUGH RECOVERY ACT FUNDING wpn10-14asep10-07aeecbg10-08a.pdf More...

466

Energy Secretary Steven Chu to Attend Grand Opening of Recovery...  

Office of Environmental Management (EM)

to Attend Grand Opening of Recovery Act-Funded A123 Systems Battery Plant Energy Secretary Steven Chu to Attend Grand Opening of Recovery Act-Funded A123 Systems Battery Plant...

467

Kraft lignin recovery by ultrafiltration: economic feasibility and impact on the kraft recovery system  

SciTech Connect (OSTI)

The widespread use of the kraft pulping process could provide a ready supply of lignin materials for many uses. Simulation studies demonstrate that recovery of the high-molecular-weight kraft lignin by ultrafiltration of a fraction of the black liquor flow is attractive from both an economic and an operational standpoint. Benefits are derived from relief of a furnace-limited recovery system and from the marketing of the lignin or modified lignin products. 10 references.

Kirkman, A.G.; Gratzl, J.S.; Edwards, L.L.

1986-05-01T23:59:59.000Z

468

Develop Thermoelectric Technology for Automotive Waste Heat Recovery...  

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

More Documents & Publications Skutterudite Thermoelectric Generator For Automotive Waste Heat Recovery Thermoelectric Conversion of Exhaust Gas Waste Heat into Usable...

469

Diesel Engine Waste Heat Recovery Utilizing Electric Turbocompound...  

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

Presentation: Caterpillar Inc. 2002deerhopmann.pdf More Documents & Publications Diesel Engine Waste Heat Recovery Utilizing Electric Turbocompound Technology Diesel...

470

Optimization Online - Sparse Recovery on Euclidean Jordan Algebras  

E-Print Network [OSTI]

Feb 3, 2013 ... Keywords: Sparse recovery on Euclidean Jordan algebra, nuclear norm minimization, restricted isometry property, null space property, ...

Lingchen Kong

2013-02-03T23:59:59.000Z

471

200,000 homes weatherized under the Recovery Act  

Broader source: Energy.gov [DOE]

Today Vice President Biden announced that the Weatherization Assistance Program has weatherized 200,000 homes under the Recovery Act.

472

Develop Thermoelectric Technology for Automotive Waste Heat Recovery...  

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

More Documents & Publications Development of Thermoelectric Technology for Automotive Waste Heat Recovery Development of Thermoelectric Technology for Automotive Waste Heat...

473

Development of More Effective Biosurfactants for Enhanced Oil Recovery  

SciTech Connect (OSTI)

The overall goal of this research was to develop effective biosurfactant production for enhanced oil recovery in the United States.

McInerney, M.J.; Mouttaki, H.; Folmsbee, M.; Knapp, R.; Nagle, D.

2003-01-24T23:59:59.000Z

474

[Waste water heat recovery system]. Final report, September 30, 1992  

SciTech Connect (OSTI)

The production capabilities for and field testing of the heat recovery system are described briefly. Drawings are included.

Not Available

1993-04-28T23:59:59.000Z

475

Determining the optimum nanofluid for enhanced oil recovery  

E-Print Network [OSTI]

Determining the optimum nanofluid for enhanced oil recovery Presented by Katie Aurand katherine and size for EOR applications Determining the optimum nanofluid for enhanced oil recovery Presented = particle modification and testing 3 Determining the optimum nanofluid for enhanced oil recovery Presented

476

The application of N,N-dimethyl-3-oxa-glutaramic acid (DOGA) in the PUREX process  

SciTech Connect (OSTI)

The new salt-free complexant, DOGA for separating trace Pu(IV) and Np(IV) from U(VI) nitric acid solution was studied. DOGA has stronger complexing abilities to Pu(IV) and Np(IV), but complexing ability of DOGA to U(VI) was weaker. The DOGA can be used in the PUREX process to separate Pu(IV) and Np(IV) from U(VI) nitric solution. On one hand, U(IV) in the nitric acid solution containing trace Pu(IV) and Np(IV) was extracted by 30%TBP - kerosene(v/v) in the presence of DOGA, but Pu(IV) and Np(IV) were kept in the aqueous phase. On the other hand, Pu(IV) and Np(IV) loading in 30% TBP - kerosene were effectively stripped by DOGA into the aqueous phase, but U(VI) loading in 30% TBP - kerosene was remained in 30% TBP - kerosene. DOGA is a promising complexant to separate Pu(IV) and Np(IV) from U(VI) solution in the U-cycle of the PUREX process. (authors)

Jianchen, Wang; Jing, Chen [Institute of Nuclear and New Energy Technology - INET, Tsinghua University, P.O. Box 1021, Beijing 102201 (China)

2007-07-01T23:59:59.000Z

477

Infiltration Heat Recovery in Building Walls: Computational Fluid Dynamics Investigations Results  

E-Print Network [OSTI]

LBNL-51324 Infiltration Heat Recovery in Building Walls: Computational Fluid Dynamics leading to partial recovery of heat conducted through the wall. The Infiltration Heat Recovery (IHR) factor was introduced to quantify the heat recovery and correct the conventional calculations

478

Microbial enhanced oil recovery and compositions therefor  

DOE Patents [OSTI]

A method is provided for microbial enhanced oil recovery, wherein a combination of microorganisms is empirically formulated based on survivability under reservoir conditions and oil recovery efficiency, such that injection of the microbial combination may be made, in the presence of essentially only nutrient solution, directly into an injection well of an oil bearing reservoir having oil present at waterflood residual oil saturation concentration. The microbial combination is capable of displacing residual oil from reservoir rock, which oil may be recovered by waterflooding without causing plugging of the reservoir rock. Further, the microorganisms are capable of being transported through the pores of the reservoir rock between said injection well and associated production wells, during waterflooding, which results in a larger area of the reservoir being covered by the oil-mobilizing microorganisms.

Bryant, Rebecca S. (Bartlesville, OK)

1990-01-01T23:59:59.000Z

479

Aqueous flooding methods for tertiary oil recovery  

DOE Patents [OSTI]

A method of aqueous flooding of subterranean oil bearing formation for tertiary oil recovery involves injecting through a well into the formation a low alkaline pH aqueous sodium bicarbonate flooding solution. The flooding solution's pH ranges from about 8.25 to 9.25 and comprises from 0.25 to 5 weight percent and preferably about 0.75 to 3.0 weight percent of sodium bicarbonate and includes a petroleum recovery surfactant of 0.05 to 1.0 weight percent and between 1 and 20 weight percent of sodium chloride. After flooding, an oil and water mixture is withdrawn from the well and the oil is separated from the oil and water mixture.

Peru, Deborah A. (Bartlesville, OK)

1989-01-01T23:59:59.000Z

480

Recovery Boiler Superheater Ash Corrosion Field Study  

SciTech Connect (OSTI)

With the trend towards increasing the energy efficiency of black liquor recovery boilers operated in North America, there is a need to utilize superheater tubes with increased corrosion resistance that will permit operation at higher temperatures and pressures. In an effort to identify alloys with improved corrosion resistance under more harsh operating conditions, a field exposure was conducted that involved the insertion of an air-cooled probe, containing six candidate alloys, into the superheater section of an operating recovery boiler. A metallographic examination, complete with corrosion scale characterization using EMPA, was conducted after a 1,000 hour exposure period. Based on the results, a ranking of alloys based on corrosion performance was obtained.

Keiser, James R [ORNL] [ORNL; Kish, Joseph [McMaster University] [McMaster University; Singbeil, Douglas [FPInnovations] [FPInnovations

2010-01-01T23:59:59.000Z

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


481

Microbial enhancement of oil recovery: Recent advances  

SciTech Connect (OSTI)

During recent years, systematic, scientific, and engineering effort by researchers in the United States and abroad, has established the scientific basis for Microbial Enhanced Oil Recovery (MEOR) technology. The successful application of MEOR technology as an oil recovery process is a goal of the Department of Energy (DOE). Research efforts involving aspects of MEOR in the microbiological, biochemical, and engineering fields led DOE to sponsor an International Conference at Brookhaven National Laboratory in 1992, to facilitate the exchange of information and a discussion of ideas for the future research emphasis. At this, the Fourth International MEOR Conference, where international attendees from 12 countries presented a total of 35 papers, participants saw an equal distribution between research'' and field applications.'' In addition, several modeling and state-of-the-art'' presentations summed up the present status of MEOR science and engineering. Individual papers in this proceedings have been process separately for inclusion in the Energy Science and Technology Database.

Premuzic, E.T.; Woodhead, A.D.; Vivirito, K.J. (eds.)

1992-01-01T23:59:59.000Z

482

Financial Recovery: Homeowner's Property Insurance Issues  

E-Print Network [OSTI]

- owner?s property insurance. Does my property insurance cover water damage? Basic property policies do not insure against flood damage. Homeown- ers have to rely on flood coverage purchased separately through FEMA?s National Flood Insurance Program (NFIP... ER-035 9-23 Financial Recovery: Homeowner?s Property Insurance Issues Nancy L. Granovsky, Professor and Extension Family Economics Specialist, The Texas A&M University System People affected by hurricanes have many questions about their home...

Granovsky, Nancy L.

2008-09-23T23:59:59.000Z

483

Waste Heat Recovery Power Generation with WOWGen  

E-Print Network [OSTI]

Waste Heat Recovery Power Generation with WOWGen? Business Overview WOW operates in the energy efficiency field - one of the fastest growing energy sectors in the world today. The two key products - WOWGen? and WOWClean? provide more... energy at cheaper cost and lower emissions. ? WOWGen? - Power Generation from Industrial Waste Heat ? WOWClean? - Multi Pollutant emission control system Current power generation technology uses only 35% of the energy in a fossil fuel...

Romero, M.

484

Cement Kiln Flue Gas Recovery Scrubber Project  

SciTech Connect (OSTI)

The Cement Kiln Flue Gas Recovery Scrubber Project was a technical success and demonstrated the following: CKD can be used successfully as the sole reagent for removing SO2 from cement kiln flue gas, with removal efficiencies of 90 percent or greater; Removal efficiencies for HCl and VOCs were approximately 98 percent and 70 percent, respectively; Particulate emissions were low, in the range of 0.005 to 0.007 grains/standard cubic foot; The treated CKD sorbent can be recycled to the kiln after its potassium content has been reduced in the scrubber, thereby avoiding the need for landfilling; The process can yield fertilizer-grade K2SO4, a saleable by-product; and Waste heat in the flue gas can provide the energy required for evaporation and crystallization in the by-product recovery operation. The demonstration program established the feasibility of using the Recovery Scrubber{trademark} for desulfurization of flue gas from cement kilns, with generally favorable economics, assuming tipping fees are available for disposal of ash from biomass combustion. The process appears to be suitable for commercial use on any type of cement kiln. EPA has ruled that CKD is a nonhazardous waste, provided the facility meets Performance Standards for the Management of CKD (U.S. Environmental Protection Agency 1999d). Therefore, regulatory drivers for the technology focus more on reduction of air pollutants and pollution prevention, rather than on treating CKD as a hazardous waste. Application of the Recovery Scrubbe{trademark} concept to other waste-disposal operations, where pollution and waste reductions are needed, appears promising.

National Energy Technology Laboratory

2001-11-30T23:59:59.000Z

485

PREDICTIVE MODELS. Enhanced Oil Recovery Model  

SciTech Connect (OSTI)

PREDICTIVE MODELS is a collection of five models - CFPM, CO2PM, ICPM, PFPM, and SFPM - used in the 1982-1984 National Petroleum Council study of enhanced oil recovery (EOR) potential. Each pertains to a specific EOR process designed to squeeze additional oil from aging or spent oil fields. The processes are: 1 chemical flooding, where soap-like surfactants are injected into the reservoir to wash out the oil; 2 carbon dioxide miscible flooding, where carbon dioxide mixes with the lighter hydrocarbons making the oil easier to displace; 3 in-situ combustion, which uses the heat from burning some of the underground oil to thin the product; 4 polymer flooding, where thick, cohesive material is pumped into a reservoir to push the oil through the underground rock; and 5 steamflood, where pressurized steam is injected underground to thin the oil. CFPM, the Chemical Flood Predictive Model, models micellar (surfactant)-polymer floods in reservoirs, which have been previously waterflooded to residual oil saturation. Thus, only true tertiary floods are considered. An option allows a rough estimate of oil recovery by caustic or caustic-polymer processes. CO2PM, the Carbon Dioxide miscible flooding Predictive Model, is applicable to both secondary (mobile oil) and tertiary (residual oil) floods, and to either continuous CO2 injection or water-alternating gas processes. ICPM, the In-situ Combustion Predictive Model, computes the recovery and profitability of an in-situ combustion project from generalized performance predictive algorithms. PFPM, the Polymer Flood Predictive Model, is switch-selectable for either polymer or waterflooding, and an option allows the calculation of the incremental oil recovery and economics of polymer relative to waterflooding. SFPM, the Steamflood Predictive Model, is applicable to the steam drive process, but not to cyclic steam injection (steam soak) processes.

Ray, R.M. [DOE Bartlesville Energy Technology Technology Center, Bartlesville, OK (United States)

1992-02-26T23:59:59.000Z

486

Investigations of nonsurgical embryo recovery in swine  

E-Print Network [OSTI]

Major Subject. : Animal Science INVESTIGATIONS OF NONSURGICAL EMBRYO RECOVERY IN SWINE A Thesis by RUSSELL LYNN ALTENHOF Approved as to style and content by: D C. K ae er (Co-Chairman of Committee) T. D. Tanksle , Jr. (Co-Chairman of Committee... and Krall, 1977). Recent evidence indicates that beta adrenegic agonists stimulate cANP- + + dependent phosphorylation and Na /K transport that + + in turn stimulated Na /Ca exchange at the plasma membrane or in the sarcoplasmic reticulum (Scheid et al...

Altenhof, Russell Lynn

1982-01-01T23:59:59.000Z

487

Improved energy recovery from geothermal reservoirs  

SciTech Connect (OSTI)

The behavior of a liquid-dominated geothermal reservoir in response to production from different horizons is studied using numerical simulation methods. The Olkaria geothermal field in Kenya is used as an example where a two-phase vapor-dominated zone overlies the main liquid-dominated reservoir. The possibility of improving energy recovery from vapor-dominated reservoirs by tapping deeper horizons is considered.

Bodvarsson, G.S.; Pruess, K.; Lippmann, M.J.

1981-01-01T23:59:59.000Z

488

HEAVY AND THERMAL OIL RECOVERY PRODUCTION MECHANISMS  

SciTech Connect (OSTI)

The Stanford University Petroleum Research Institute (SUPRI-A) conducts a broad spectrum of research intended to help improve the recovery efficiency from difficult to produce reservoirs including heavy oil and fractured low permeability systems. Our scope of work is relevant across near-, mid-, and long-term time frames. The primary functions of the group are to conduct direction-setting research, transfer research results to industry, and educate and train students for careers in industry. Presently, research in SUPRI-A is divided into 5 main project areas. These projects and their goals include: (1) Multiphase flow and rock properties--to develop better understanding of the physics of displacement in porous media through experiment and theory. This category includes work on imbibition, flow in fractured media, and the effect of temperature on relative permeability and capillary pressure. (2) Hot fluid injection--to improve the application of nonconventional wells for enhanced oil recovery and elucidate the mechanisms of steamdrive in low permeability, fractured porous media. (3) Mechanisms of primary heavy oil recovery--to develop a mechanistic understanding of so-called ''foamy oil'' and its associated physical chemistry. (4) In-situ combustion--to evaluate the effect of different reservoir parameters on the insitu combustion process. (5) Reservoir definition--to develop and improve techniques for evaluating formation properties from production information. What follows is a report on activities for the past year. Significant progress was made in all areas.

Anthony R. Kovscek; Louis M. Castanier

2002-09-30T23:59:59.000Z

489

SURFACTANT - POLYMER INTERACTION FOR IMPROVED OIL RECOVERY  

SciTech Connect (OSTI)

The goal of this research is to use the interaction between a surfactant and a polymer for efficient displacement of tertiary oil by improving slug integrity, adsorption and mobility control. Surfactant--polymer flooding has been shown to be highly effective in laboratory-scale linear floods. The focus of this proposal is to design an inexpensive surfactant-polymer mixture that can efficiently recover tertiary oil by avoiding surfactant slug degradation high adsorption and viscous/heterogeneity fingering. A mixture comprising a ''pseudo oil'' with appropriate surfactant and polymer has been selected to study micellar-polymer chemical flooding. The physical properties and phase behavior of this system have been determined. A surfactant-polymer slug has been designed to achieve high efficiency recovery by improving phase behavior and mobility control. Recovery experiments have been performed on linear cores and a quarter 5-spot. The same recovery experiments have been simulated using a commercially available simulator (UTCHEM). Good agreement between experimental data and simulation results has been achieved.

Unknown

1998-10-01T23:59:59.000Z

490

Imaging of CO2 injection during an enhanced-oil-recovery experiment  

E-Print Network [OSTI]

Injection during an Enhanced-Oil-Recovery Experiment RolandEnergy (DOE) as an enhanced oil recovery (EOR) project, was

Gritto, Roland; Daley, Thomas M.; Myer, Larry R.

2003-01-01T23:59:59.000Z

491

Proposed Guideline Clarifications for American Recovery and Reinvestment Act of 2009  

E-Print Network [OSTI]

th align="right" valign="top">CFDA: Design Recovery> 1642990396473 CFDA>2004031CFDA> CFDA-title>Design Recovery Transparency

Wilde, Erik; Kansa, Eric C; Yee, Raymond

2009-01-01T23:59:59.000Z

492

Removing oxygen from a solvent extractant in an uranium recovery process  

DOE Patents [OSTI]

An improvement in effecting uranium recovery from phosphoric acid solutions is provided by sparging dissolved oxygen contained in solutions and solvents used in a reductive stripping stage with an effective volume of a nonoxidizing gas before the introduction of the solutions and solvents into the stage. Effective volumes of nonoxidizing gases, selected from the group consisting of argon, carbon dioxide, carbon monoxide, helium, hydrogen, nitrogen, sulfur dioxide, and mixtures thereof, displace oxygen from the solutions and solvents thereby reduce deleterious effects of oxygen such as excessive consumption of elemental or ferrous and accumulation of complex iron phosphates or cruds.

Hurst, Fred J. (Oak Ridge, TN); Brown, Gilbert M. (Knoxville, TN); Posey, Franz A. (Concord, TN)

1984-01-01T23:59:59.000Z

493

Method for oxygen reduction in a uranium-recovery process. [US DOE patent application  

DOE Patents [OSTI]

An improvement in effecting uranium recovery from phosphoric acid solutions is provided by sparging dissolved oxygen contained in solutions and solvents used in a reductive stripping stage with an effective volume of a nonoxidizing gas before the introduction of the solutions and solvents into the stage. Effective volumes of nonoxidizing gases, selected from the group consisting of argon, carbon dioxide, carbon monoxide, helium, hydrogen, nitrogen, sulfur dioxide, and mixtures thereof, displace oxygen from the solutions and solvents thereby reduce deleterious effects of oxygen such as excessive consumption of elemental or ferrous iron and accumulation of complex iron phosphates or cruds.

Hurst, F.J.; Brown, G.M.; Posey, F.A.

1981-11-04T23:59:59.000Z

494

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

DOE Patents [OSTI]

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

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

1996-08-13T23:59:59.000Z

495

Development of a Novel Solvent for the Simultaneous Separation of Strontium and Cesium from Acidic Solutions  

SciTech Connect (OSTI)

A synergistic extraction solvent for the simultaneous removal of cesium and strontium from acidic solutions has been investigated. The extraction solvent consists of, 4,4',(5')-di-(t-butyldicyclo-hexano)-18-crown-6 (DtBuCH18C6), calix[4]arene-bis-(tert-octylbenzo-crown-6) (BOBCalixC6), and 1-(2,2,3,3-tetrafluoropropoxy)-3-(4-sec-butylphenoxy)-2-propanol (Cs-7SB modifier) in a branched aliphatic kerosene (Isopar® L). Extraction synergy for strontium was observed when DtBuCH18C6 was combined with the BOBCalixC6 cesium extractant solvent and Cs-7SB modifier or if the Cs-7SB modifier was substituted into the SREX (Strontium Extraction) solvent in place of TBP. The novel process extracted both cesium and strontium simultaneously from 1 M nitric acid solutions with distribution ratios of 8.8 and 7.7 for strontium and cesium, respectively, at ambient temperature. Distribution coefficients for cesium and strontium as a function of nitric acid concentration and temperature were also obtained with 0.5 M<[HNO3]<2.5 M giving favorable distribution ratios. This new process utilizing the combined solvent has been named the Fission Product Extraction Process (FPEX).

Catherine L. Riddle; John D. Baker; Jack D. Law; Christopher A. McGrath; David H. Meikrantz; Bruce J. Mincher; Dean R. Peterman; Terry A. Todd

2005-03-01T23:59:59.000Z

496

Hot Corrosion at Air-Ports in Kraft Recovery Boilers  

SciTech Connect (OSTI)

Hot corrosion can occur on the cold-side of airports in Kraft recovery boilers. The primary corrosion mechanism involves the migration of sodium hydroxide and potassium hydroxide vapors through leaks in the furnace wall at the airports and their subsequent condensation. It has been reported that stainless steel is attacked much faster than carbon steel in composite tubes, and that carbon steel tubing, when used with a low-chromium refractory, does not exhibit this type of corrosion. For hot corrosion fluxing of metal oxides, either acidic or basic fluxing takes place, with a solubility minimum at the basicity of transition between the two reactions. For stainless steel, if the basicity of the fused salt is between the iron and chromium oxide solubility minima, then a synergistic effect can occur that leads to rapid corrosion. The products of one reaction are the reactants of the other, which eliminates the need for rate-controlling diffusion. This effect can explain why stainless steel is attacked more readily than carbon steel.

Holcomb, Gordon R.; Covino, Bernard S., Jr.; Russell, James H.

2003-01-01T23:59:59.000Z

497

APPLICATION OF FORMOHYDROXAMIC ACID IN NUCLEAR PROCESSING: SYNTHESIS AND COMPLEXATION WITH TECHNETIUM-99  

SciTech Connect (OSTI)

Acetohydroxamic acid (AHA) is an organic ligand planned for use in the Uranium Extraction (UREX) process. It reduces neptunium and plutonium, and the resultant hydrophilic complexes are separated from uranium by extraction with tributyl phosphate (TBP) in a hydrocarbon diluent. AHA undergoes hydrolysis to acetic acid which will impede the recycling of nitric acid. During recent discussions of the UREX process, it has been proposed to replace AHA by formohydroxamic acid (FHA). FHA will undergo hydrolysis to formic acid which is volatile, thus allowing the recycling of nitric acid. The reported reduction potentials of AHA and pertechnetate (TcO{sub 4}{sup -}) indicated that it may be possible for AHA to reduce technetium, altering its fate in the fuel cycle. At UNLV, it has been demonstrated that TcO{sub 4}{sup -} undergoes reductive nitrosylation by AHA under a variety of conditions. The resulting divalent technetium is complexed by AHA to form the pseudo-octahedral trans-aquonitrosyl (diacetohydroxamic)-technetium(II) complex ([Tc{sup II}(NO)(AHA){sub 2}H{sub 2}O]{sup +}). In this paper, we are reporting the synthesis of FHA and its complex formation with technetium along with the characterization of FHA crystals achieved by NMR and IR spectroscopy. Two experiments were conducted to investigate the complexation of FHA with Tc and the results were compared with previous data on AHA. The first experiment involved the elution of Tc from a Reillex HP anion exchange resin, and the second one monitored the complexation of technetium with FHA by UV-visible spectrophotometry.

Amber Wright; Edward Mausolf; Keri Campbell; Frederic Poineau; P. Paviet-Hartmann

2010-05-01T23:59:59.000Z

498

Approaches for regeneration of amine-carboxylic acid extracts  

SciTech Connect (OSTI)

Extraction processes based on reversible chemical complexation can be useful for separation of polar organics from dilute solution. Tertiary amines are effective extractants for the recovery of carboxylic acids from aqueous solution. The regeneration of aminecarboxylic acid extracts is an important step which strongly influences the economic viability of the separation process. Several regeneration methods are critically reviewed, and the factors that affect swing regeneration processes, including temperature-swing, diluent composition-swing and pH-swing with a volatile base are discussed. Interest in this area comes from interest in treatment of waste streams, particularly in petrochemical and fermentation manufacture.

Dai, Y.; King, C.J.

1995-07-01T23:59:59.000Z

499

Heat recovery and seed recovery development project: preliminary design report (PDR)  

SciTech Connect (OSTI)

The preliminary design and performance characteristics are described of the 20 MWt heat recovery and seed recovery (HRSR) system to be fabricated, installed, and evaluated to provide a technological basis for the design of commercial size HRSR systems for coal-fired open-cycle MHD power plants. The system description and heat and material balances, equipment description and functional requirements, controls, interfacing systems, and operation and maintenance are detailed. Appendices include: (1) recommended environmental requirements for compliance with federal and state of Tennessee regulations, (2) channel and diffuser simulator, (3) equipment arrangement drawings, and (4) channel and diffuser simulator barrel drawings. (WHK)

Arkett, A. H.; Alexander, K. C.; Bolek, A. D.; Blackman, B. K.; Kurrle, P. E.; Tram, S. V.; Warren, A. M.; Ziobrowski, A. J.

1981-06-01T23:59:59.000Z

500

Recovery of yttrium from fluorescent powder of cathode ray tube, CRT: Zn removal by sulphide precipitation  

SciTech Connect (OSTI)

Highlights: • Treatment of fluorescent powder of CRT waste. • Factorial experimental designs to study acid leaching of fluorescent powder and the purification of leach liquors. • Recover of yttrium by precipitation using oxalic acid. • Suitable flowsheet to recover yttrium from fluorescent powder. - Abstract: This work is focused on the recovery of yttrium and zinc from fluorescent powder of cathode ray tube (CRT). Metals are extracted by sulphuric acid in the presence of hydrogen peroxide. Leaching tests are carried out according to a 2{sup 2} full factorial plan and the highest extraction yields for yttrium and zinc equal to 100% are observed under the following conditions: 3 M of sulphuric acid, 10% v/v of H{sub 2}O{sub 2} concentrated solution at 30% v/v, 10% w/w pulp density, 70 °C and 3 h of reaction. Two series of precipitation tests for zinc are carried out: a 2{sup 2} full factorial design and a completely randomized factorial design. In these series the factors investigated are pH of solution during the precipitation and the amount of sodium sulphide added to precipitate zinc sulphide. The data of these tests are used to describe two empirical mathematical models for zinc and yttrium precipitation yields by regression analysis. The highest precipitation yields for zinc are obtained under the following conditions: pH equal to 2–2.5% and 10–12% v/v of Na{sub 2}S concentrated solution at 10% w/v. In these conditions the coprecipitation of yttrium is of 15–20%. Finally further yttrium precipitation experiments by oxalic acid on the residual solutions, after removing of zinc, show that yttrium could be recovered and calcined to obtain the final product as yttrium oxide. The achieved results allow to propose a CRT recycling process based on leaching of fluorescent powder from cathode ray tube and recovery of yttrium oxide after removing of zinc by precipitation. The final recovery of yttrium is 75–80%.

Innocenzi, Valentina, E-mail: valentina.innocenzi1@univaq.it [Department of Industrial Engineering and Information and Economy, University of L’Aquila, Via Giovanni Gronchi n.18, Nucleo Ind.le di Pile, 67100 L’Aquila (Italy); De Michelis, Ida; Ferella, Francesco [Department of Industrial Engineering and Information and Economy, University of L’Aquila, Via Giovanni Gronchi n.18, Nucleo Ind.le di Pile, 67100 L’Aquila (Italy); Beolchini, Francesca [Department of Marine Sciences, Polytechnic Institute of Marche, Via Brecce Bianche, 60131 Ancona (Italy); Kopacek, Bernd [SAT, Austrian Society for Systems Engineering and Automation, Gurkasse 43/2, A-1140 Vienna (Austria); Vegliò, Francesco [Department of Industrial Engineering and Information and Economy, University of L’Aquila, Via Giovanni Gronchi n.18, Nucleo Ind.le di Pile, 67100 L’Aquila (Italy)

2013-11-15T23:59:59.000Z