WorldWideScience

Sample records for boiling nitric acid

  1. Corrosion fatigue behavior of zirconium in boiling nitric acid

    International Nuclear Information System (INIS)

    The corrosion fatigue behavior of zirconium in boiling nitric acid has been studied to evaluate the reliability of zirconium used in nuclear fuel reprocessing equipment. An apparatus designed for corrosion fatigue tests in boiling nitric acid was used. The crack growth rate of zirconium was measured as a function of the stress intensity factor using TDCB type specimens. After the tests, the fracture morphology was examined with a scanning electron microscope. The crack growth rate was influenced with the texture of specimens and the test environments. In air at room temperature, the crack growth rate at the longitudinal direction of specimens was faster than that of the transverse direction. Moreover, the crack growth rate in boiling nitric acid was more faster than that in air at room temperature. According to the fractographic examination, X-ray analysis, and so on, the observed results were interpreted with based on the crystal anisotropy on mechanical properties and the susceptibility to stress corrosion cracking in boiling nitric acid of zirconium. (author)

  2. Thermodynamic study on redox reactions of boiling nitric acid solutions

    International Nuclear Information System (INIS)

    In order to understand corrosion of metals in nitric acid solutions, it is necessary to know the generation mechanism of high equilibrium potential in the solutions, especially under boiling conditions. Existing nitrogen oxides in nitric acid solutions were first analyzed by Raman spectroscopy and then existing amount of nitrogen oxides were examined by thermodynamic calculation using the SOLGASMIX software. The Raman spectroscopic analysis showed that the existing amount of un-dissociated HNO3 increased with increasing nitric acid concentration and solution temperature. The existing amount of NO2 also increased by thermal decomposition. The thermodynamic calculation showed that the important nitrogen oxides in nitric acid solutions are HNO3, NO3-, HNO2, NO2, and NO. The equilibrium potential of nitric acid solution is, however, mainly decided by the HNO3/HNO2 equilibrium. The thermodynamic calculation also suggested that the increased oxidization potential on the heat-transfer surface is attributed to the reduction of nitrous acid concentration by the thermal decomposition of nitrous acid on the surface and the continuous removal of decomposition product from the solutions by boiling babbles. (author)

  3. Fatigue crack propagation behaviors of zirconium and Ti-5Ta alloy in boiling nitric acid

    International Nuclear Information System (INIS)

    Fatigue crack propagation behaviors of zirconium (Zr) and titanium-5%tantalum (Ti-5Ta) alloy in boiling nitric acid were investigated by fatigue tests. The crack propagation rates (CPR) of them were measured as a function of the stress intensity factor range, ΔK. CPR of Zr in boiling nitric acid was markedly enhanced as compared with that in air at room temperature. On the other hand, any environmental acceleration effect and any fractographic difference were not observed in CPR tests of Ti-5Ta alloy. The fractograph of Zr tested in the nitric acid showed a river pattern type crack. The enhancement effect on CPR of Zr was interpreted with high susceptibility to stress corrosion cracking (SCC) in boiling nitric acid. (author)

  4. Influence of Oxide Film to Stress Corrosion Cracking of Zirconium in Boiling Nitric Acid Solution

    International Nuclear Information System (INIS)

    Nuclear fuel reprocessing process acts an important role of nuclear energy cycle. In Japan, a commercial reprocessing plant has been operating at the Rokkasho reprocessing plant. Purex process that is used nitric acid and dodecane with tributyl phosphate for solvent has been adopted in the plant. Boiling nitric acid is applied to dissolve oxide spent nuclear fuel. In the boiling nitric acid solution, plant material corrodes severely and intergranular corrosion is observed in stainless steels. In order to avoid corrosion in such severe environment, some equipment in the plants has been made of zirconium, which has excellent corrosion resistance in nitric acid solutions. However, it has been known that zirconium has stress corrosion cracking (SCC) susceptibility in concentrated HNO3 with nobler corrosion potential. Nobler corrosion potential causes breakdowns of passive film having excellent protective performance and raises SCC susceptibility of zirconium in nitric acid solutions. Therefore, it is important to clarify the relationship among potential, growth and the breakdown of oxide film for the SCC initiation mechanism. In this study, we investigated the oxide film growth of zirconium with various potentials in boiling nitric acid solutions. Electrochemical tests and immersion tests with various applied potentials conducted in boiling 3. 6 and 9 mol.dm-3 HNO3. The potentials in the immersion tests were set at 1.3, 1.4 and 1.5 V vs. sat. KCl-Ag/AgCl electrode (SSE). These were in the region of trans-passive state of zirconium in boiling nitric acid solution. The test durations were 10, 100 and 500 h. After the corrosion tests, cross-sectional observations of oxide films were conducted. From the results of anodic polarization curves of zirconium in boiling nitric acid, passivity region was observed through rest potential to about 1.5 V in boiling 6 mol.dm-3 HNO3. Rapid increase of current density was observed at the potential attributed to transition from passivity

  5. Corrosion of high purity Fe-Cr-Ni alloys in 13 N boiling nitric acid

    International Nuclear Information System (INIS)

    Corrosion in boiling nitric acid was investigated for high purity Fe-18%Cr-12%Ni alloys and type 304L stainless steels (SS). Owing to very low impurity concentration, the solution treated high purity alloys show almost no intergranular corrosion while the type 304L SS show severe intergranular corrosion. Both in the high purity alloys and type 304L SS, aging treatments ranging from 873 K to 1073 K for 1 h enhance intergranular corrosion. During the aging treatments, impurities should be segregated to the grain boundaries. The corrosion behaviors were discussed from a standpoint of impurity segregation to grain boundaries. This study is of importance for purex reprocessing of spent fuels

  6. Corrosion studies in fuel element reprocessing environments containing nitric acid

    International Nuclear Information System (INIS)

    Nitric acid is universally used in aqueous fuel element reprocessing plants; however, in the processing scheme being developed by the Consolidated Fuel Reprocessing Program, some of the equipment will be exposed to nitric acid under conditions not previously encountered in fuel element reprocessing plants. A previous report presented corrosion data obtained in hyperazeotropic nitric acid and in concentrated magnesium nitrate solutions used in its preparation. The results presented in this report are concerned with the following: (1) corrosion of titanium in nitric acid; (2) corrosion of nickel-base alloys in a nitric acid-hydrofluoric acid solution; (3) the formation of Cr(VI), which enhances corrosion, in nitric acid solutions; and (4) corrosion of mechanical pipe connectors in nitric acid. The results show that the corrosion rate of titanium increased with the refreshment rate of boiling nitric acid, but the effect diminished rapidly as the temperature decreased. The addition of iodic acid inhibited attack. Also, up to 200 ppM of fluoride in 70% HNO3 had no major effect on the corrosion of either titanium or tantalum. In boiling 8 M HNO3-0.05 M HF, Inconel 671 was more resistant than Inconel 690, but both alloys experienced end-grain attack. In the case of Inconel 671, heat treatment was very important; annealed and quenched material was much more resistant than furnace-cooled material.The rate of oxidation of Cr(III) to Cr(VI) increased significantly as the nitric acid concentration increased, and certain forms of ruthenium in the solution seemed to accelerate the rate of formation. Mechanical connectors of T-304L stainless steel experienced end-grain attack on the exposed pipe ends, and seal rings of both stainless steel and a titanium alloy (6% Al-4% V) underwent heavy attack in boiling 8 M HNO3

  7. 49 CFR 173.158 - Nitric acid.

    Science.gov (United States)

    2010-10-01

    ... 2.5 L (0.66 gallon) capacity each. (f) Nitric acid of 70 percent or less concentration, when offered... 49 Transportation 2 2010-10-01 2010-10-01 false Nitric acid. 173.158 Section 173.158... Nitric acid. (a) Nitric acid exceeding 40 percent concentration may not be packaged with any...

  8. Nitric Acid Poisoning: Case Report

    International Nuclear Information System (INIS)

    Nitric acid (HNO3) is a corrosive fluid that, when in contact with reducing agents, generates nitrogen oxides that are responsible for inhalation poisoning. We present two cases of poisoning from nitric acid gas inhalation resulting from occupational exposure. Imaging findings were similar in both cases, consistent with adult respiratory distress syndrome (ARDS): bilaterally diffuse alveolar opacities on the chest X-ray and a cobblestone pattern on computed tomography (CT).one of the patients died while the other evolved satisfactorily after treatment with n-acetyl cysteine and mechanical ventilation. The diagnosis of nitric acid poisoning was made on the basis of the history of exposure and the way in which the radiological findings evolved.

  9. Refractory Oxide Coatings on Titanium for Nitric Acid Applications

    Science.gov (United States)

    Ravi Shankar, A.; Kamachi Mudali, U.

    2014-07-01

    Tantalum and Niobium have good corrosion resistance in nitric acid as well as in molten chloride salt medium encountered in spent fuel nuclear reprocessing plants. Commercially, pure Ti (Cp-Ti) exhibits good corrosion resistance in nitric acid medium; however, in vapor condensates of nitric acid, significant corrosion was observed. In the present study, a thermochemical diffusion method was pursued to coat Ta2O5, Nb2O5, and Ta2O5 + Nb2O5 on Ti to improve the corrosion resistance and enhance the life of critical components in reprocessing plants. The coated samples were characterized by XRD, SEM, EDX, profilometry, micro-scratch test, and ASTM A262 Practice-C test in 65 pct boiling nitric acid. The SEM micrograph of the coated samples showed that uniform dense coating containing Ta2O5 and/or Nb2O5 was formed. XRD patterns indicated the formation of TiO2, Ta2O5/Nb2O5, and mixed oxide/solid solution phase on coated Ti samples. ASTM A262 Practice-C test revealed reproducible outstanding corrosion resistance of Ta2O5-coated sample in comparison to Nb2O5- and Ta2O5 + Nb2O5-coated sample. The hardness of the Ta2O5-coated Cp-Ti sample was found to be twice that of uncoated Cp-Ti. The SEM and XRD results confirmed the presence of protective oxide layer (Ta2O5, rutile TiO2, and mixed phase) on coated sample which improved the corrosion resistance remarkably in boiling liquid phase of nitric acid compared to uncoated Cp-Ti and Ti-5Ta-1.8Nb alloy. Three phase corrosion test conducted on Ta2O5-coated samples in boiling 11.5 M nitric acid showed poor corrosion resistance in vapor and condensate phases of nitric acid due to poor adhesion of the coating. The adhesive strength of the coated samples needs to be optimized in order to improve the corrosion resistance in vapor and condensate phases of nitric acid.

  10. Ruthenium nitrosyl complexes in nitric acid solutions

    International Nuclear Information System (INIS)

    Nine nitrosyl ruthenium complexes have been separated and identified in aqueous solutions of nitric acid. The separation method was low temperature, gradient elution, reverse phase partition chromatography using tri-n-butyl phosphate on a kiesel gel 60 support using 106Ru labelled complexes in the nitric acid phase. The identification of the complexes was deduced from the relationships between the products of aquation and nitration and paper chromatography using both methyl-iso-propyl ketone and nitric acid-acetone elutions. The proportion of each complex at equilibrium in various concentrations of nitric acid have been measured. The rates of nitration in 10 M nitric acid, and of aquation in 0.45 M nitric acid have been determined at 00C. (author)

  11. Decomposition of molybdenite products with nitric acid

    International Nuclear Information System (INIS)

    The problems of development abroad of hydrometallurgic methods of opening molybdenum concentrates using nitric acid are considered. Several variants of the process are developed, they are the two-stage decomposition by stoichiometrically necessary amount of nitric acid, single-stage decomposition in the avtoclave using nitric acid and oxigen as oxidizers; decomposition using circulatina nitro-sulfuric solution containing molybdenum. The advantages and disadvantages of new methods are presented

  12. Decomposition of molybdenite products with nitric acid

    Energy Technology Data Exchange (ETDEWEB)

    Nikitina, L.S.

    1983-04-01

    The problems of development abroad of hydrometallurgic methods of opening molybdenum concentrates using nitric acid are considered. Several variants of the process are developed, they are the two-stage decomposition by stoichiometrically necessary amount of nitric acid, single-stage decomposition in the autoclave using nitric acid and oxigen as oxidizers; decomposition using circulatina nitro-sulfuric solution containing molybdenum. The advantages and disadvantages of new methods are presented.

  13. Redox behavior of chromium on the corrosion of austenitic stainless steel (R-SUS304ULC) in 8 M nitric acid solution

    International Nuclear Information System (INIS)

    We investigated the relationship between the corrosion of austenitic stainless steel (R-SUS304ULC) and the redox behavior of chromium in nitric acid solution under three conditions – boiling at atmospheric pressure, boiling at reduced pressure, and non-boiling – to evaluate the effects of the boiling phenomenon. In the Cr(III) oxidation rate measurement, about 20% of the Cr(III) was oxidized to Cr(VI) under atmospheric-pressure boiling at 384 K after 168 h. Under non-boiling conditions at 373 K, Cr(VI) was not observed. However, about 3% of Cr(III) oxidation was observed at 373 K with reduced-pressure boiling. Thermodynamic calculations showed that the abundance of Cr(VI) in boiling nitric acid was increased over that in non-boiling nitric acid, even at the same temperature. These results show that Cr(III) is more likely to oxidize under boiling conditions than non-boiling conditions. On the other hand, in the corrosion tests, we found that the apparent reduction rate of Cr(VI) as a result of corrosion of R-SUS304ULC was more than 10 times greater than the Cr(III) oxidation rate. Therefore, the corrosion of R-SUS304ULC appears to be dominated by the rate of Cr(VI) reduction in nitric acid solution regardless of the boiling or non-boiling conditions. (author)

  14. Nitrogen isotope exchange in between nitric oxide and nitric acid

    International Nuclear Information System (INIS)

    The exchange rate law experimentally observed for 15 N/14 N exchange in NO - HNO3 system at low nitric acid concentration, both at atmospheric pressure and at low pressure of NO: R k[H+][NO3-][HNO2], is identical with the rate law for the reaction between NO and HNO3, when HNO2 is formed.The rate of nitrogen isotope exchange between NO and HNO3 has been measured as a function of nitric acid concentration of 1.5 4 M.l-1. The exchange rate law is shown to be R k[HNO3]2[N2O3] and the measured activation energy is E = 67.78 kJ.M-1. It is concluded that N2O3 participates in 15 N/14 N exchange between NO and HNO3 at nitric acid concentration higher than 1.5 M.l-1. The rate of the same isotope exchange in NO - HNO3 system has been also measured as a function of nitric oxide pressure 0.1 0.4 M.Pa for 1 and 2 M.l-1 HNO3. It is demonstrated that 15 N/14 N exchange in this system has a linear dependence on NO pressure as indicated by rate measurements at different NO partial pressures and constant overall pressure, by adding helium in reactor. Using the rate law presented above the nitrogen isotope exchange rate for nitric acid concentration 1.5 10 M.l-1 were calculated. Nitrogen isotope exchange between nitric oxide and concentrated nitric acid with a single stage separation factor = 1.055, for 10 M.l-1 nitric acid, at 25 deg. C, provides the bases for 15 N separation process that is most widely used at the present time, i.e. the method of Spindel and Taylor. In order to know what happens in 15N separation at higher pressure, when the isotopic transport is improved, a stainless steel laboratory experimental plant with a 1000 mm long and 18 mm i.d. column, packed with triangular wire springs of 1.8 x 1.8 x 0.2 mm, was utilised. At 1.5 atm (absolute) and 2.36 ml.cm-2.min-1 flow rate, HETP was 7% smaller than at atmospheric pressure and 1.5 times smaller flow rate. The operation of 15 N separation plant at 1.8 atm (absolute), instead atmospheric pressure, will permit doubling

  15. Electrochemical Behavior of Aluminum in Nitric Acid

    Institute of Scientific and Technical Information of China (English)

    CHEN; Hui; ZHU; Li-yang; LIN; Ru-shan; TAN; Hong-bin; HE; Hui

    2013-01-01

    Aluminum is one of cladding materials for nuclear fuel,it is important to investigate the electrolytic dissolution of aluminum in nitric acid.The electrochemical impedance spectroscopy,polarization curve and cyclic voltammetry cure of anodic aluminum electrode in nitric acid under various conditions were collected(Fig.1).It turns out,under steady state,the thickness of the passivated film of aluminum

  16. Boils

    Science.gov (United States)

    ... the boil is very bad or comes back. Antibacterial soaps and creams cannot help much once a boil ... following may help prevent the spread of infection: Antibacterial soaps Antiseptic (germ-killing) washes Keeping clean (such as ...

  17. Extraction of metal nitrates and nitric acid

    International Nuclear Information System (INIS)

    The effects of the extraction of nitric acid with nondiluted dialkylphosphoric acids have been studied. The investigation used the physical-chemical method allowing to determine the compositions of compounds in organic phase and to describe the equilibrium in a wide concentration range of distributed chemical. The solvate compositions determined from the dependence of the effective nitric acid distribution constant in extraction with nondiluted dibutyl (DBPA) and di-2-ethyl-hexylphosphoric (D2EHPA) acids on the function of equilibrium water activity agree with different reported physical-chemical methods of research. Thermodynamic distribution and extraction constants have been calculated and tabulated for the formation and organic phase of dissociated and nondissociated disolvates, as well as monosolvates of nitric acid

  18. Modeling acid-gas generation from boiling chloride brines

    OpenAIRE

    Sonnenthal Eric; Spycher Nicolas; Zhang Guoxiang; Steefel Carl

    2009-01-01

    Abstract Background This study investigates the generation of HCl and other acid gases from boiling calcium chloride dominated waters at atmospheric pressure, primarily using numerical modeling. The main focus of this investigation relates to the long-term geologic disposal of nuclear waste at Yucca Mountain, Nevada, where pore waters around waste-emplacement tunnels are expected to undergo boiling and evaporative concentration as a result of the heat released by spent nuclear fuel. Processes...

  19. Boils

    Science.gov (United States)

    ... or recurrent boils, which are usually due to Staph infections. The bacteria are picked up somewhere and then ... version of boils is folliculitis . This is an infection of hair follicles, usually with Staph bacteria. These often itch more than hurt. The ...

  20. Nitric-phosphoric acid oxidation of organic waste materials

    International Nuclear Information System (INIS)

    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 NOx 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

  1. Containment of nitric acid solutions of Plutonium-238

    Science.gov (United States)

    Reimus, M. A. H.; Silver, G. L.; Pansoy-Hjelvik, L.; Ramsey, K. B.

    1999-01-01

    The corrosion of various metals that could be used to contain nitric acid solutions of Pu-238 has been studied. Tantalum and tantalum/2.5% tungsten resisted the test solvent better than 304L stainless steel and several INCONEL alloys. The solvent used to imitate nitric acid solutions of Pu-238 contained 70% nitric acid, hydrofluoric acid, and ammonium hexanitratocerate.

  2. Phase equilibrium liquid-vapour in the nitrogen dioxide-nitric acid system

    International Nuclear Information System (INIS)

    Nitrogen dioxide being used as a coolant in some nuclear facilities, its production chemistry and purification techniques are of practical interest. The experimental dependence is obtained of the boiling temperature on the solution composition of nitric acid in nitrogen dioxide and of nitrogen dioxide in nitric acid at the atmospheric pressure by use of Cotrell's ebulliometer. The numerical solution of Gibbs-Duhem's equation in view of solution heats of the components gives the parameters of the phase equilibrium liquid-vapour. The results obtained are tabulated and recommended for designing rectification processes

  3. On the Influence of Nitrates on the Composition of Vapour Phase over Nitric Acid Solutions

    International Nuclear Information System (INIS)

    The paper contains the experimental data for vapour liquid equilibrium and boiling-point temperatures at a pressure of 760 mm Hg, for part of the nitrate - nitric acid - water systems. The authors study systems with nitrates of Al, Fe, Mg, Cu, Na and NH4. They describe in general terms a manner of calculating the evaporation process in waste solutions obtained from the reprocessing of irradiated fuel elements. The high-activity, nitric-acid waste solutions are formed during the extractive reprocessing of irradiated fuel elements. These solutions themselves constitute complex systems, composed of a series of nitrates, in addition to volatile components such as water and nitric acid. Evaporation is usually carried out to reduce the volume of the waste solutions before burial, and in the course of evaporation, nitric acid is driven off. The nitrates in the waste solutions have a definite influence on the distribution of nitric acid between the vapour and liquid phases during evaporation. The work described consists of an attempt to determine this influence for each nitrate, by investigating the vapour/liquid equilibrium in part of the nitrate - nitric acid - water systems. (author)

  4. Modeling acid-gas generation from boiling chloride brines

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Guoxiang; Spycher, Nicolas; Sonnenthal, Eric; Steefel, Carl

    2009-11-16

    This study investigates the generation of HCl and other acid gases from boiling calcium chloride dominated waters at atmospheric pressure, primarily using numerical modeling. The main focus of this investigation relates to the long-term geologic disposal of nuclear waste at Yucca Mountain, Nevada, where pore waters around waste-emplacement tunnels are expected to undergo boiling and evaporative concentration as a result of the heat released by spent nuclear fuel. Processes that are modeled include boiling of highly concentrated solutions, gas transport, and gas condensation accompanied by the dissociation of acid gases, causing low-pH condensate. Simple calculations are first carried out to evaluate condensate pH as a function of HCl gas fugacity and condensed water fraction for a vapor equilibrated with saturated calcium chloride brine at 50-150 C and 1 bar. The distillation of a calcium-chloride-dominated brine is then simulated with a reactive transport model using a brine composition representative of partially evaporated calcium-rich pore waters at Yucca Mountain. Results show a significant increase in boiling temperature from evaporative concentration, as well as low pH in condensates, particularly for dynamic systems where partial condensation takes place, which result in enrichment of HCl in condensates. These results are in qualitative agreement with experimental data from other studies. The combination of reactive transport with multicomponent brine chemistry to study evaporation, boiling, and the potential for acid gas generation at the proposed Yucca Mountain repository is seen as an improvement relative to previously applied simpler batch evaporation models. This approach allows the evaluation of thermal, hydrological, and chemical (THC) processes in a coupled manner, and modeling of settings much more relevant to actual field conditions than the distillation experiment considered. The actual and modeled distillation experiments do not represent

  5. Modeling acid-gas generation from boiling chloride brines

    International Nuclear Information System (INIS)

    This study investigates the generation of HCl and other acid gases from boiling calcium chloride dominated waters at atmospheric pressure, primarily using numerical modeling. The main focus of this investigation relates to the long-term geologic disposal of nuclear waste at Yucca Mountain, Nevada, where pore waters around waste-emplacement tunnels are expected to undergo boiling and evaporative concentration as a result of the heat released by spent nuclear fuel. Processes that are modeled include boiling of highly concentrated solutions, gas transport, and gas condensation accompanied by the dissociation of acid gases, causing low-pH condensate. Simple calculations are first carried out to evaluate condensate pH as a function of HCl gas fugacity and condensed water fraction for a vapor equilibrated with saturated calcium chloride brine at 50-150 C and 1 bar. The distillation of a calcium-chloride-dominated brine is then simulated with a reactive transport model using a brine composition representative of partially evaporated calcium-rich pore waters at Yucca Mountain. Results show a significant increase in boiling temperature from evaporative concentration, as well as low pH in condensates, particularly for dynamic systems where partial condensation takes place, which result in enrichment of HCl in condensates. These results are in qualitative agreement with experimental data from other studies. The combination of reactive transport with multicomponent brine chemistry to study evaporation, boiling, and the potential for acid gas generation at the proposed Yucca Mountain repository is seen as an improvement relative to previously applied simpler batch evaporation models. This approach allows the evaluation of thermal, hydrological, and chemical (THC) processes in a coupled manner, and modeling of settings much more relevant to actual field conditions than the distillation experiment considered. The actual and modeled distillation experiments do not represent

  6. Modeling acid-gas generation from boiling chloride brines

    Directory of Open Access Journals (Sweden)

    Sonnenthal Eric

    2009-11-01

    Full Text Available Abstract Background This study investigates the generation of HCl and other acid gases from boiling calcium chloride dominated waters at atmospheric pressure, primarily using numerical modeling. The main focus of this investigation relates to the long-term geologic disposal of nuclear waste at Yucca Mountain, Nevada, where pore waters around waste-emplacement tunnels are expected to undergo boiling and evaporative concentration as a result of the heat released by spent nuclear fuel. Processes that are modeled include boiling of highly concentrated solutions, gas transport, and gas condensation accompanied by the dissociation of acid gases, causing low-pH condensate. Results Simple calculations are first carried out to evaluate condensate pH as a function of HCl gas fugacity and condensed water fraction for a vapor equilibrated with saturated calcium chloride brine at 50-150°C and 1 bar. The distillation of a calcium-chloride-dominated brine is then simulated with a reactive transport model using a brine composition representative of partially evaporated calcium-rich pore waters at Yucca Mountain. Results show a significant increase in boiling temperature from evaporative concentration, as well as low pH in condensates, particularly for dynamic systems where partial condensation takes place, which result in enrichment of HCl in condensates. These results are in qualitative agreement with experimental data from other studies. Conclusion The combination of reactive transport with multicomponent brine chemistry to study evaporation, boiling, and the potential for acid gas generation at the proposed Yucca Mountain repository is seen as an improvement relative to previously applied simpler batch evaporation models. This approach allows the evaluation of thermal, hydrological, and chemical (THC processes in a coupled manner, and modeling of settings much more relevant to actual field conditions than the distillation experiment considered. The actual

  7. Plutonium removal from nitric acid waste streams

    International Nuclear Information System (INIS)

    Separations research at the Rocky Flats Plant (RFP) has found ways to significantly improve plutonium secondary recovery from nitric acid waste streams generated by plutonium purifications operations. Capacity and breakthrough studies show anion exchange with Dowex 1.4 (50-100 mesh) to be superior for secondary recovery of plutonium. Extraction chromatography with TOPO (tri-n-octyl-phosphine oxide) on XAD-4 removes the final traces of plutonium, including hydrolytic polymer

  8. Study of lanthanide leaching from phosphosemihydrate by nitric acid

    International Nuclear Information System (INIS)

    Nitric acid leaching of lanthanides from phosphosemihydrate (PSH) prepared by treating the Khibiny apatite concentrate at nitric acid concentration of 2-8% and S:L ratio 1:3 was studied under laboratory conditions. Results of experiments are compared with the data obtained during sulfuric acid leaching. It is shown that during one-stage process nitric acid leaches lanthanides from PSH more effectively that sulfuric acid. However, in case of multiple use of the same solution for successive leaching of several portion of PSH, accumulation of lanthanides in nitric acid solutions occurs less intensively than in sulfuric acid ones

  9. K Basin Sludge Conditioning Testing: Nitric Acid Dissolution Testing of K East Canister Sludge

    International Nuclear Information System (INIS)

    This report describes tests performed by Pacific Northwest National Laboratory (PNNL) for Numatec Hanford Corporation (NHC) as part of the overall activities for the development of the K Basin Sludge Treatment System. These tests were conducted to examine the dissolution behavior of a K East Basin canister sludge composite in nitric acid at the following concentrations: 2 M, 4 M, 6 M, 7.8 M and 10 M and temperatures of 25 C and boiling. Assuming that the sludge was 100% uranium metal, a 4X stoichiometric excess of nitric acid was used for all testing, except that conducted at 4 M. In the 4 M nitric acid dissolution test, 50% excess nitric acid was used resulting in a dissolver solution with a significantly higher solids loading. The boiling tests were conducted for 11 hr, the 25 C dissolution tests were conducted from 24 hr to 2 weeks. For the 25 C dissolution testing, the weight percent residual solids was determined, however, chemical and radiochemical analyses were not performed

  10. Effect of neptunium ions on corrosion of stainless steel in nitric acid solution

    International Nuclear Information System (INIS)

    We have studied corrosion of a stainless steel in nitric acid solution containing neptunium. Using type 304L stainless steel, corrosion tests in boiling neptunium nitrate solution were conducted under immersion and heat-transfer condition. By the weight loss measurement of stainless steel and the quantitative analysis of metallic ions dissolved in solution, the corrosion rates of stainless steel were obtained. The surface morphology was observed by scanning electron microscopy. The corrosion acceleration mechanism was investigated by polarization measurement and spectrophotometry. The corrosion rate of stainless steel was accelerated by addition of neptunium in nitric acid solution. Preferential intergranular corrosion was observed. The corrosion of stainless steel was promoted under heat-transfer condition compared to immersion condition. In polarization measurements, the cathodic over-voltage was decreased; the cathodic current was increased by addition of neptunium. Spectrophotometric measurements showed the oxidization of neptunium in boiling nitric acid. The corrosion mechanism in nitric acid solution containing neptunium suggested the re-oxidation of neptunium. (author)

  11. Containment of nitric acid solutions of Plutonium-238

    International Nuclear Information System (INIS)

    The corrosion of various metals that could be used to contain nitric acid solutions of Pu-238 has been studied. Tantalum and tantalum/2.5% tungsten resisted the test solvent better than 304L stainless steel and several INCONEL alloys. The solvent used to imitate nitric acid solutions of Pu-238 contained 70% nitric acid, hydrofluoric acid, and ammonium hexanitratocerate. copyright 1999 American Institute of Physics

  12. Growth of nitric acid hydrates on thin sulfuric acid films

    Science.gov (United States)

    Iraci, Laura T.; Middlebrook, Ann M.; Wilson, Margaret A.; Tolbert, Margaret A.

    1994-05-01

    Type I polar stratospheric clouds (PSCs) are thought to nucleate and grow on stratospheric sulfate aerosols (SSAs). To model this system, thin sulfuric acid films were exposed to water and nitric acid vapors (1 - 3 × 10-4 Torr H2O and 1 - 2.5 × 10-6 Torr HNO3) and subjected to cooling and heating cycles. FTIR spectroscopy was used to probe the phase of the sulfuric acid and to identify the HNO3/H2O films that condensed. Nitric acid trihydrate (NAT) was observed to grow on crystalline sulfuric acid tetrahydrate (SAT) films. NAT also condensed in/on supercooled H2SO4 films without causing crystallization of the sulfuric acid. This growth is consistent with NAT nucleation from ternary solutions as the first step in PSC formation.

  13. Growth of nitric acid hydrates on thin sulfuric acid films

    Science.gov (United States)

    Iraci, Laura T.; Middlebrook, Ann M.; Wilson, Margaret A.; Tolbert, Margaret A.

    1994-01-01

    Type I polar stratospheric clouds (PSCs) are thought to nucleate and grow on stratospheric sulfate aerosols (SSAs). To model this system, thin sulfuric acid films were exposed to water and nitric acid vapors (1-3 x 10(exp -4) Torr H2O and 1-2.5 x 10(exp -6) Torr HNO3) and subjected to cooling and heating cycles. Fourier Transform Infrared (FTIR) spectroscopy was used to probe the phase of the sulfuric acid and to identify the HNO3/H2O films that condensed. Nitric acid trihydrate (NAT) was observed to grow on crystalline sulfuric acid tetrahydrate (SAT) films. NAT also condensed in/on supercooled H2SO4 films without causing crystallization of the sulfuric acid. This growth is consistent with NAT nucleation from ternary solutions as the first step in PSC formation.

  14. Nitrous oxides desorption from nitric acid (58–60 wt. %)

    OpenAIRE

    Литвиненко, Олександр Олександрович; Печенко, Тамара Ивановна; Подустов, Михаил Алексеевич; Букатенко, Алексей Иванович

    2015-01-01

    The process of nitrous oxides desorption from nitric acid solutions (in domestic schemes) was considered. It is shown that in the process of desorption (or stripping), the nitrous oxides are not removed from solutions completely, so, the nitric acid does not satisfy the technical requirements in Ukraine.The research objective was to bring the quality of nitric acid to technological standards by removing (stripping) nitrous oxides from its solutions.To achieve the research objective, the balan...

  15. Actinide removal from nitric acid waste streams

    International Nuclear Information System (INIS)

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

  16. The kinetics of the 15N/14N isotopic exchange between nitric oxide and nitric acid

    International Nuclear Information System (INIS)

    The rate of the 15N isotopic exchange between NO-NHO3 at high nitric acid concentration (2-10M) have been measured. The experimental data were obtained by contacting nitric oxide at atmospheric pressure with nitric acid solution labelled with 15N, in a glass contactor. The measurements were carried out in a glass vessel with magnetic stirrer maintaining always the same stirring rate (17 rot.s-1). The temperature was kept constant at 25 +-0.5 deg C. The reaction vessel was connected to a vacuum line and a purified nitric oxide source. The rate of the isotopic exchange and of the nitric oxide absorption in nitric acid were determined with a gas-burette in the simple apparatus described earlier. (T.G.)

  17. Composition of nitrosyl ruthenium complexes in nitric acid

    International Nuclear Information System (INIS)

    The composition of nitrosyl ruthenium complexes in nitric acid has been determined. The analysis was carried out by low temperature, gradient elution, reversed-phase partition chromatography. Paper chromatography, using methyl isopropyl ketone and nitric acid-acetone, were also carried out to obtain complementary data. (author)

  18. Method of evaporizing ruthenium-containing nitric acid

    International Nuclear Information System (INIS)

    Purpose: To improve the ruthenium decontamination coefficient in nitric acid recovered in the step of dissolving spent fuels into nitric acid in fuel reprocessing. Method: Ruthenium contained as fission products is formed into nitrosyl complex compounds under the effect of nitrogen oxides present together upon dissolving into nitric acid. The complex compounds of nitrosyl ruthenium are decomposed when heated in concentrated nitric acid and, when oxidized further, form volatile ruthenium tetraoxide and evaporized together with nitric acid vapors to reduce the decontaminating coefficients of a nitric acid distillating device. In this invention, the heating time is shortened and the decomposing amount is decreased in the distillating concentration of nitric acid solutions thereby improving the decontaminating coefficients in the distillator by utilizing the fact that the decomposing rate of the nitrosyl ruthenium complex compounds is not always rapid. It is thus possible to improve the decontaminating coefficients up to a limit value determined by the entrainment of liquid droplets and, in addition, corrosion of austenite type stainless steels due to the competition between nitric acid and ruthenium can be improved. (Horiuchi, T.)

  19. Electrochemical corrosion investigations on austenitic CrNi-steels in nitric acid with and without additions of metal ions

    International Nuclear Information System (INIS)

    The aim of the present work was to develop an electrochemical short-time test procedure for detecting intergranular corrosion (IGC) susceptibility of austenitic CrNi-steels in strongly oxidizing media, as e.g. concentrated nitric acid. This procedure should cover the test parameters of the usually applied ASTM Standard Huey Test, which is performed in boiling 14.4 n nitric acid. The described electrochemical test procedure - a potentiostatic polarisation of steel specimens in the transpassive range - is presented as an alternative to the Huey Test with equivalent results, but with a reduced testing time. (orig./IHOE)

  20. Studies of molybdenite interaction with nitric acid

    Energy Technology Data Exchange (ETDEWEB)

    Potashnikov, Yu.M.; Lutsik, V.I.; Chursanov, Yu.V. (Kalininskij Politekhnicheskij Inst. (USSR))

    1984-01-01

    Products composition and their effect on the reaction rate of molybdenite with nitric acid are specified. It is shown that alongside with NO, NO/sub 2/ is included in the composition of the products of MoS/sub 2/ and HNO/sub 3/ interaction, and it produces catalytic effect on the process considered. Under the conditions studied, MoS/sub 2/ dissolution proceeds in the mixed regime, conditioned by similar values of molybdenite oxidation rate and reaction product diffusion into solution volume (Esub(act.=28.9 kJ/mol, K/sub 298/=6.3x10/sup -7/, cmxs/sup -1/), and for that to catalytic effect of NO/sub 2/ the dependence V approximately ..cap alpha..sup(-g.37) is observed.

  1. Studies of molybdenite interaction with nitric acid

    International Nuclear Information System (INIS)

    Product composition and their effect on the reaction rate of molybdenite with nitric acid are specified. It is shown that alongside with NO NO2 is included in the composition of the products of MoS2 and HNO3 interaction and it produces catalytic effect on the process considered. Under the conditions studied MoS2 dissolution proceeds in the mixed regime, conditioned by similar values of molybdenite oxidation rate and reaction product diffusion into solution volume (Esub(act.=28.9 kJ/mol, K298=6.3x10-7, cmxs-1), at that due to catalytic effect of NO2 the dependence V approximately αsup(-g.37) is observed

  2. Studies on the reaction of nitric acid and sugar

    International Nuclear Information System (INIS)

    The design of vessels and off-gas systems for denitrating acidic radioactive process solutions by reacting nitric acid with sugar requires a fairly accurate determination of the rate of the controlling step. Therefore, the reaction of sugar with concentrated nitric acid was closely examined at temperatures of 100 and 1100C and in the presence of low levels of iron )0 to 0.2 M Fe(III)). Efficiencies of the sugar destruction by nitric acid ranged from 2.56 to 2.93 mol of acid consumed per mole of carbon added. Product off-gases were examined throughout the reaction. Release of CO was fairly constant throughout the reaction, but amounts of CO2 increased as the nitric acid began to attack the terminal carboxylic acids produced from the consumption of sucrose. Voluminous quantities of NO2 were released at the beginning of the reaction, but larger relative concentrations of NO were observed toward the end

  3. Adverse experiences with nitric acid at the Savannah River Site

    Energy Technology Data Exchange (ETDEWEB)

    Durant, W.S.; Craig, D.K.; Vitacco, M.J.; McCormick, J.A.

    1991-06-01

    Nitric acid is used routinely at the Savannah River Site (SRS) in many processes. However, the site has experienced a number of adverse situations in handling nitric acid. These have ranged from minor injuries to personnel to significant explosions. This document compiles many of these events and includes discussions of process upsets, fires, injuries, and toxic effects of nitric acid and its decomposition products. The purpose of the publication is to apprise those using the acid that it is a potentially dangerous material and can react in many ways as demonstrated by SRS experience. 10 refs.

  4. Nitric acid uptake by sulfuric acid solutions under stratospheric conditions - Determination of Henry's Law solubility

    Science.gov (United States)

    Reihs, Christa M.; Golden, David M.; Tolbert, Margaret A.

    1990-01-01

    The uptake of nitric acid by sulfuric acid solutions representative of stratospheric particulate at low temperatures was measured to determine the solubility of nitric acid in sulfuric acid solutions as a function of H2SO4 concentration and solution temperature. Solubilities are reported for sulfuric acid solutions ranging from 58 to 87 wt pct H2SO4 over a temperature range from 188 to 240 K, showing that, in general, the solubility of nitric acid increases with decreasing sulfuric acid concentration and with decreasing temperature. The measured solubilities indicate that nitric acid in the global stratosphere will be found predominantly in the gas phase.

  5. Leaching of sodium carbonate cakes by nitric acid

    International Nuclear Information System (INIS)

    The interaction has been studied of soda cakes of fluorite-rare-earth concentrate with nitric acid. The effect of a number of factors on extraction of REE into a nitric solution has been considered: the final acidity of the pulp, the duration of leaching, and the ratio between solid and liquid phases. The effect of adding aluminium nitrate into the pulp has also been studied. It has been shown that three-stage counterflow leaching of soda cakes with nitric acid increases REE extraction approximately by 10%

  6. Thermal Stability of Acetohydroxamic Acid/Nitric Acid Solutions

    International Nuclear Information System (INIS)

    The transmutation of transuranic actinides and long-lived fission products in spent commercial nuclear reactor fuel has been proposed as one element of the Advanced Accelerator Applications Program. Preparation of targets for irradiation in an accelerator-driven subcritical reactor would involve dissolution of the fuel and separation of uranium, technetium, and iodine from the transuranic actinides and other fission products. The UREX solvent extraction process is being developed to reject and isolate the transuranic actinides in the acid waste stream by scrubbing with acetohydroxamic acid (AHA). To ensure that a runaway reaction will not occur between nitric acid and AHA, an analogue of hydroxyl amine, thermal stability tests were performed to identify if any processing conditions could lead to a runaway reaction

  7. Nitric-phosphoric acid oxidation of solid and liquid organic materials

    International Nuclear Information System (INIS)

    Nitric-phosphoric acid oxidation has been developed specifically to address issues that face the Savannah River Site, other defense-related facilities, private industry, and small-volume generators such as university and medical laboratories. Initially tested to destroy and decontaminate SRS solid, Pu-contaminated job-control waste, the technology has also exhibited potential for remediating hazardous and mixed-hazardous waste forms. The process is unique to Savannah River and offers a valuable alternative to other oxidation processes that require extreme temperatures and/or elevated pressures. To address the broad categories of waste, many different organic compounds which represent a cross-section of the waste that must be treated have been successfully oxidized. Materials that have been quantitatively oxidized at atmospheric pressure below 180 degrees C include neoprene, cellulose, EDTA, tributylphosphate, and nitromethane. More stable compounds such as benzoic acid, polyethylene, oils, and resins have been completely decomposed below 200 degrees C and 10 psig. The process uses dilute nitric acid in a concentrated phosphoric acid media as the main oxidant for the organic compounds. Phosphoric acid allow nitric acid to be retained in solution well above its normal boiling point. The reaction forms NOx vapors which can be reoxidized and recycled using air and water. The addition of 0.001M Pd(II) reduces CO generation to near 1% of the released carbon gases. The advantages of this process are that it is straightforward, uses relatively inexpensive reagents, operates at relatively low temperature and pressure, and produces final solutions which are compatible with stainless steel equipment. For organic wastes, all carbon, hydrogen, and nitrogen are converted to gaseous products. If interfaced with an acid recovery system which converts NOx back to nitric acid, the net oxidizer would be oxygen from air

  8. Tropospheric measurements of nitric acid vapor and particulate nitrate

    International Nuclear Information System (INIS)

    Measurements of tropospheric nitric acid and particulate nitrate concentrations as a function of altitude in various marine and continental areas generally free from urban pollution are presented. Air was sampled at altitudes from 0.2 to 8 km, above and within the boundary layer, from 54 deg S to 70 deg N using impregnated filter technology. Most of the samples taken in the northern mid-latitude continental region are observed to contain greater than 0.1 ppbv nitric acid, while the rest of the samples contained significantly less. Particulate nitrate concentrations range from generally less than 0.2 ppbm above the boundary layer to 1.4 ppbm in the continental, urban-influenced boundary layer. Nitric acid is found to exceed particulate nitrate above the boundary layer, however to be considerably less in the marine boundary layer. Implications of these measurements for one-dimensional models of nitric acid gradients and global nitrogen oxide budgets are discussed

  9. NOx generation method from recovered nitric acid by electrolysis

    International Nuclear Information System (INIS)

    A considerable amount of sodium nitrate solution is generated as low-level liquid waste in a spent-fuel reprocessing plant. If the nitric acid recovered from the low-level liquid waste is decomposed into useful materials, such as NOx gas, the nitric acid can be reused and the volume of low-level liquid waste can be greatly reduced. Studies were conducted on electrolytic reduction as a technology for reducing waste volume and producing NOx gas directly from recovered nitric acid in the reprocessing plant. As a result of fundamental research, it was found that NOx could be produced at high current efficiency if nitric acid of 5 - 6 mol/liter or more is electrolytically reduced with graphite or platinum electrodes. (author)

  10. The Iron-Catalyzed Oxidation of Hydrazine by Nitric Acid

    Energy Technology Data Exchange (ETDEWEB)

    Karraker, D.G.

    2001-07-17

    To assess the importance of iron to hydrazine stability, the study of hydrazine oxidation by nitric acid has been extended to investigate the iron-catalyzed oxidation. This report describes those results.

  11. Nitric acid leaching of polymetallic middlings of concentration

    OpenAIRE

    Rogozhnikov, D. A.; Mamyachenkov, S. V.; Karelov, S. V.; Anisimova, O. S.

    2013-01-01

    Investigations into the nitric acid leaching of polymetallic middlings with the purpose of the maximal recovery of copper and zinc into the solution are performed. Using methods of mathematical planning of the experiment, the optimal process parameters are determined: ratio L: S = 5, the consumption of nitric acid is 80 cm3 per 20 g of the charge, and the process duration is 120 min. © 2013 Allerton Press, Inc.

  12. Nitric acid adduct formation during crystallization of barium and strontium nitrates and their co-precipitation from nitric acid media

    International Nuclear Information System (INIS)

    The molar solubilities of Ba, Sr and Pb nitrates in nitric acid as a function of total nitrate concentration is presented and described by the mass action law, indicating on formation of the adducts with nitric acid. Precipitates of Ba(NO3)2 and Sr(NO3)2 crystallized from nitric acid were studied by ISP OES and IR spectroscopy. The data obtained confirmed formation of metastable adducts with nitric acid. IR and X-ray diffraction studies of the mixed salt systems indicated conversion of the mixed salts into (Ba,Sr)(NO3)2 solid solution of discrete structure in range of total nitrate ion concentration ∼6 mol/L. (author)

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

    International Nuclear Information System (INIS)

    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±0.092 at 25 C, and extraction enthalpy is -5. 46±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 x 106±3.56 x 104 at 25 C; reaction enthalpy was -9.610±0.594 kcal/mol. Nitration complexation constant is 8.412±0.579, with an enthalpy of -10.72±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

  14. Tested Demonstrations: Color Oscillations in the Formic Acid-Nitric Acid-Sulfuric Acid System.

    Science.gov (United States)

    Raw, C. J. G.; And Others

    1983-01-01

    Presented are procedures for demonstrating the production of color oscillations when nitric acid is added to a formic acid/concentrated sulfuric acid mixture. Because of safety considerations, "Super-8" home movie of the color changes was found to be satisfactory for demonstration purposes. (JN)

  15. Nitric acid measurements in connection with corrosion studies

    Science.gov (United States)

    Ferm, Martin; De Santis, Franco; Varotsos, Costas

    Atmospheric nitric acid does not only contribute to acidification and eutrophication but causes also deterioration of many materials. Material belonging to our cultural heritage is irreplaceable and its lifetime can depend on the corrosion rate. Nowadays, only very few long-term measurements of nitric acid concentration in Europe and elsewhere have been published so far. Due to the fact that atmospheric corrosion is a long-term effect, the relevant research does not necessarily require monitoring of nitric acid on a daily basis. Moreover, power supply is often not available at sites where it is of interest to study the corrosion rate of objects belonging to our cultural heritage. Besides, such measurements must not disturb the impression of the objects. In this context, the diffusive sampling technique provides average concentrations over long-term periods at a low cost. In addition, the samplers used are noiseless, comparatively small in size, and thus, their ambient exposure can be made inconspicuously and with discretion. The present paper is focussed on an intensive corrosion study, which was performed at 11 rural and 23 urban sites in Europe and one rural site in Canada during 2002/2003. For the above-mentioned reasons, the diffusive sampler's technique was employed for the nitric acid monitoring, where the diffusive samplers were first tested against the denuder technique and bi-monthly measurements of nitric acid were thus obtained. The bi-monthly concentrations varied from 0.05 to 4.3 μg m -3 and the annual averages from 0.16 to 2.0 μg m -3. The observations collected, depicted a summertime maximum and a wintertime minimum in the nitric acid concentrations, except at the northern rural sites, where a maximum in the winter was observed. Furthermore, the observed nitric acid concentrations in Southern Europe were higher than in Northern Europe. In a few places, close to the sites of urban measurements, rural measurements of nitric acid were also performed

  16. Removal of iodine species by concentrated nitric acid, (2)

    International Nuclear Information System (INIS)

    One of the most effective removing processes of iodine species is what is called ''Iodox Process'', which contains oxidation and absorption of iodine species by highly concentrated nitric acid. The result of fundamental test with bubble column in this process had been reported. Present paper describes the fundamental experiment by the use of packed column. This experiment has been carried out to clear the effect of feed gas flow rate, nitric acid flow rate, nitric acid concentration, and methyl iodide concentration on removal efficiency of methyl iodide. The following results were obtained. The decontamination factor of methyl iodide (DF) increases exponentially with nitric acid concentration, which agrees with the result obtained by using the bubble column. The factor is in inverse proportion to feed gas flow rate, and is also almost independent of nitric acid flow rate and methyl iodide concentration. The relation between the decontamination factor and the capacity coefficient has been examined, and then the experimental equations of the capacity coefficient and the decontamination factor on this fundamental experiment have been estimated. (author)

  17. [Determination of serum vitamin B12 and folic acid by non boil (new standard) radioassay].

    Science.gov (United States)

    Ishiwata, Y; Tuchii, K; Endo, N; Ikeda, R; Yasuda, K

    1994-06-01

    On purpose to study the radioassay of serum vitamin B12 and folic acid using non boil methods in with these two vitamins were released from their endogenous binding proteins with alkaline denaturation and separated the bound vitamins from the free ones with the magnetic iron particles coated these vitamin binders (purified hog intrinsic factor and beta-lactoglobulin from cow milk) were evaluated on precision and accuracy, compared with boil radioassay. 1. The reproducibilities of non boil method were 4.5 +/- 2.5% on vit. B12 and 3.5 +/- 0.2% on folate (n = 10), respectively. 2. The recovery test of the two serum vitamins with the use of cyanocobalamin and pteroylglutamic acid (J.P.) were finely showed the rations of 95.2-99.0% for vit. B12 and 101.0-108.0% for folic acid. And that of folic acid use of 5-methyl-tetrahydro-pteroylglutamic acid was showed the ratios of 101.0-104.0%. The values of folic acid measured by this method were found slightly higher than non boil method using conventional standard. 3. The correlation coefficient between non boil method and boil method were 0.987 and regression equation was showed y = 0.97x + 73.59 for vit. B12 (n = 75) and r = 0.932, y = 1.02x-0.08 (n = 78) for folic acid. 4. Normal range of serum total vit. B12 concentration was 210-920 (484 +/- 160 pg/ml, n = 259) and that of folic acid was 2.5-9.2 (5.2 +/- 1.4 ng/ml, n = 257), as well as boil method. 5. Accordingly it was considered that non boil (new standard) method was excellent for estimation of vitamin B12 and folic acid clinical status. PMID:8072237

  18. Dissolution of unirradiated UO2-pellets in nitric acid

    International Nuclear Information System (INIS)

    Cinetics of dissolution of UO2-pellets in nitric acid and the gaseous reaction products, N2O, NO, NO2 are determined for different temperatures and acid concentrations. NO2:NO ratio increases with temperature and nitrate concentration. The amount of N2O formed increases with temperature and acid concentration. At 900C and dissolution in 12 m nitric acid 1l weight-% of UO2 are dissolved forming N2O. The oxidation of UO2 takes place on the crystal surface or at the interface UO2/HNO3. U(IV)-ions cannot be detected in the solution. The nitrous acid resulting from reduction of HNO3 or the species which is in equilibrium with nitrous acid e.g. the nitrosyl-ion is responsible for UO2-oxidation. (orig./PW)

  19. Separation of ruthenium from nitric acid solutions using carbon tetrachloride

    International Nuclear Information System (INIS)

    The noble metal, ruthenium is one of the major fission product elements produced with high fission yield, mainly in for breeder reactors using 239Pu fuels. In the aqueous reprocessing of spent fuels for the recovery of U and Pu by PUREX process ruthenium interferes in the solvent extraction stage. In the treatment of high level liquid waste for its disposal, oxides of Ru are formed, which contaminate the surrounding environment owing to their high vapour pressure. Hence, it is desirable to separate from the waste solution prior to its processing for disposal. A simple and feasible method has been employed in the present work for the separation and recovery of ruthenium from aqueous nitric acid medium using ammonium ceric nitrate (ACN) and carbon tetrachloride (CCl4). The efficiency in the separation of Ru was investigated under various experimental conditions such as acidity and ageing effect. Separation efficiency was observed to decrease with increasing nitric acid concentration. Maximum separation was achieved at 1 M nitric acid. Further studies were carried out to investigate the effect of ageing on the separation efficiency ruthenium. With increase in time, separation percentage of ruthenium was decreasing in all concentrations of nitric acid studied. (author)

  20. Electrochemical behavior of plutonium in nitric acid media

    International Nuclear Information System (INIS)

    The first step of the spent nuclear fuel reprocessing is a dissolution of actinides and fission products in hot nitric acid at high concentration. Among all these species, the knowledge of redox plutonium equilibria with discerning between their oxidation states is essential to understand and depended on many chemical conditions. Nevertheless, the knowledge of speciation in this media is a challenge especially for a better understanding of corrosion mechanism in the dissolution medium. Thus this paper proposes to determine the electrochemical behaviour of plutonium and especially the Pu(IV)/Pu(III), Pu(VI)/ Pu(V) and Pu(V)/Pu(IV) redox couple in nitric acid media and acquire thermodynamic and kinetic constants at higher temperatures than 25 deg C and higher nitric concentration than 1 mol L-1. (author)

  1. Removal of plutonium from nitric acid-oxalic acid solutions using anion exchange method

    International Nuclear Information System (INIS)

    An anion exchange method using Amberlyst A-26 (MP) resin was developed for removal of Pu from nitric acid-oxalic acid solutions without destroying oxalate. The method consists of sorption of Pu(IV) on Amberlyst A-26, a macroporous anion exchange resin, from nitric acid-oxalic acid medium in the presence of Al(NO3)3. Pu(IV) breakthrough capacity of Amberlyst A-26 using synthetic feed solution was determined. (author)

  2. Aluminium dissolution for spray pulverization with nitric acid

    International Nuclear Information System (INIS)

    A comparative study of the nitric acid dissolution of aluminium, by immersion and spray pulverization has been carried out in laboratory scale. As a result, the optimum operation conditions to control reaction in the plant are fixed. Operation costs are also evaluated. (author)

  3. Nitric acid flowsheet with late wash PHA testing

    International Nuclear Information System (INIS)

    This Task Technical Plan outlines the activities to be conducted in the Integrated DWPF Melter System (IDMS) in ongoing support of the Defense Waste Processing Facility (DWPF) Chemical Process Cell (CPC) utilizing the Nitric Acid Flowsheet in the Sludge Receipt and Adjustment Tank (SRAT) and Precipitate Hydrolysis Aqueous (PHA) produced by the Late Wash Flowsheet. The IDMS facility is to be operated over a series of runs (2 to 4) using the Nitric Acid Flowsheet. The PHA will be produced with the Late Wash Flowsheet in the Precipitate Hydrolysis Experimental Facility (PHEF). All operating conditions shall simulate the expected DWPF operating conditions as closely as possible. The task objectives are to perform at least two IDMS runs with as many operating conditions as possible at nominal DWPF conditions. The major purposes of these runs are twofold: verify that the combined Late Wash and Nitric Acid flowsheets produce glass of acceptable quality without additional changes to process equipment, and determine the reproducibility of data from run to run. These runs at nominal conditions will be compared to previous runs made with PHA produced from the Late Wash flowsheet and with the Nitric Acid flowsheet in the SRAT (Purex 4 and Purex 5)

  4. The nitric acid burn trauma of the skin.

    Science.gov (United States)

    Kolios, L; Striepling, E; Kolios, G; Rudolf, K-D; Dresing, K; Dörges, J; Stürmer, K M; Stürmer, E K

    2010-04-01

    Nitric acid burn traumata often occur in the chemical industry. A few publications addressing this topic can be found in the medical database, and there are no reports about these traumata in children. A total of 24 patients, average 16.6 years of age, suffering from nitric acid traumata were treated. Wound with I degrees burns received open therapy with panthenol-containing creams. Wound of II degrees and higher were initially treated by irrigation with sterile isotonic saline solution and then by covering with silver-sulphadiazine dressing. Treatment was changed on the second day to fluid-absorbent foam bandages for superficial wounds (up to IIa degrees depth) and occlusive, antiseptic moist bandages in combination with enzymatic substances for IIb degrees -III degrees burns. After the delayed demarcation, necrectomy and mesh-graft transplantation were performed. All wounds healed adequately. Chemical burn traumata with nitric acid lead to specific yellow- to brown-stained wounds with slower accumulation of eschar and slower demarcation compared with thermal burns. Remaining wound eschar induced no systemic inflammation reaction. After demarcation, skin transplantation can be performed on the wounds, as is commonly done. The distinguishing feature of nitric-acid-induced chemical burns is the difficulty in differentiation and classification of burn depth. An immediate lavage should be followed by silver sulphadiazine treatment. Thereafter, fluid-absorbent foam bandages or occlusive, antiseptic moist bandages should be used according to the burn depth. Slow demarcation caused a delay in performing surgical treatments. PMID:19875347

  5. Oxidation of coal-based raw materials by nitric acid

    Czech Academy of Sciences Publication Activity Database

    Novák, J.; Novák, František; Madronová, L.; Machovič, V.; Kozler, J.

    New York : Nova Science Publisher, 2011 - (Madronová, L.), s. 105-123 ISBN 978-1-61668-965-0. - ( Chemistry Research and Applications ) Institutional research plan: CEZ:AV0Z60660521 Keywords : oxidation * coal-based raw materials * nitric acid Subject RIV: CB - Analytical Chemistry , Separation

  6. The stability of N, N-dimethylhydroxylamine in nitric acid

    International Nuclear Information System (INIS)

    The purity of N, N-dimethylhydroxylamine(DMHAN) has been analyzed and the results indicate that the DMHAN synthesized by ourself contains few impurities and meets the needs of the experiment. A titration method for determination of the concentration of DMHAN has been established based on the potassium dichromate titration after the ferric oxidation. The ratio of DMHAN to ferric in the oxidation of DMHAN is found to be 1:4. Methanol, formaldehyde, and formic acid, which are possible oxidized products of DMHAN, do not influence the result of analysis. Using this titration method, the stability of DMHAN in nitric acid has been studied and we found that the decomposition of DMHAN in nitric acid depends on temperature and the concentration of nitric acid: the decomposition of DMHAN increases with the increasing of acidity and temperature although the concentration of DMHAN has little change under certain acidity and temperature, and DMHAN is decomposed quickly when the temperature is higher than 35 degree C and the acidity is higher than 3.0 mol/L. (authors)

  7. Uranium sorption from nitric acid solutions by cationites and polyampholytes

    International Nuclear Information System (INIS)

    Sorption of uranium ions with KU-2 x 8 sulfonic cation exchanger, KFP-12 phosphoric acid cation exchanger and aminophosphoric acid ampholytes was examined in nitric acid solutions containing different amounts of HNO3. Formation of polymeric complexes was confirmed by IR spectra. The ion-coordination mechanism of U sorption with KFP-12 cation exchanger was clearly manifested; sorption of U as a single-charged nitrate complex ion is also possible. The isotherms of sorption of the U ions with KFP-12 cation exchanger have a convex shape with a sharply ascending portion at low U concentrations, which is favorable for U recovery from raffinate solutions. Nitrogen-phosphorus-containing polyampholytes also possess a high sorption power with respect to the U ions in nitric acid solutions. The highest exchange capacity is exhibited by polyacrylate base ANKF-80 and ANKF-86 polyampholytes

  8. 77 FR 48433 - New Source Performance Standards Review for Nitric Acid Plants

    Science.gov (United States)

    2012-08-14

    ... Federal Register on December 23, 1971 (36 FR 24881). The first review of the Nitric Acid Plants NSPS was... requirements for new nitric acid production units? IV. Summary of Significant Changes Since Proposal A. How is..., Energy, and Economic Impacts of These Standards A. What are the impacts for Nitric Acid Production...

  9. 76 FR 63878 - New Source Performance Standards Review for Nitric Acid Plants

    Science.gov (United States)

    2011-10-14

    ... of the Nitric Acid Plants NSPS was completed on June 19, 1979 (44 FR 35265). An additional review was... ) emission limit, which applies to each nitric acid production unit commencing construction, modification, or... questions about these proposed standards for nitric acid production units, contact Mr. Chuck French,...

  10. Actinide and lanthanide extraction from nitric acid solutions by flotation

    International Nuclear Information System (INIS)

    Flotation of thorium, plutonium(IV), uranium(VI) and gadolinium from aqueous nitric acid solutions (HNO3) was investigated using lauryl phosphoric acid (LPA) as a SAS-collector. It is established that the extent of removal of the metal ions increases with the amount of LPA introduced, regardless of the solution acidity. It is shown that in principle ∼ 100% extraction of plutonium(IV) and thorium by flotation is possible regardless of the acidity of aqueous solutions. Ca(NO3)2 added to the system does not significantly affect the flotation extraction of thorium. (author) 14 refs.; 5 figs

  11. Buffering effects on electrograining of aluminium in nitric acid

    Energy Technology Data Exchange (ETDEWEB)

    Koroleva, E.V. [Corrosion and Protection Centre, UMIST, P.O. Box 88, Manchester M60 1QD (United Kingdom)]. E-mail: e.koroleva@umist.ac.uk; Thompson, G.E. [Corrosion and Protection Centre, UMIST, P.O. Box 88, Manchester M60 1QD (United Kingdom); Skeldon, P. [Corrosion and Protection Centre, UMIST, P.O. Box 88, Manchester M60 1QD (United Kingdom); Hollrigl, G. [Alcan Technology and Management Ltd., Bad. Bahnhofstrasse 16, CH-8212 Neuhausen (Switzerland); Lockwood, S. [Bridgnorth Aluminium Limited, Stourbridge Road, Bridgnorth WV15 6AU (United Kingdom); Smith, G. [Bridgnorth Aluminium Limited, Stourbridge Road, Bridgnorth WV15 6AU (United Kingdom)

    2005-09-01

    Electrograining of a binary Al-Si alloy has been undertaken in nitric acid based electrolytes, with the resultant surfaces examined by scanning and transmission electron microscopies. Depending on electrograining conditions, the pit appearance varies from hemispherical to large lateral pits, with the latter favoured in relatively acidic electrolytes. The conditions prevailing in the pit have been explored through use of aluminium ion additions to the nitric acid electrolyte as well as additions of species which influence the precipitation and dissolution of aluminium hydroxide. These confirm that control of the pit solution pH, through hydroxide generation, as a result of the selected electrograining conditions and consequent anodic and cathodic polarisation, enables tailoring of the resultant electrograined surface appearance.

  12. What Is the Boiling Point and Heat of Vaporization of Sulfuric Acid?

    Science.gov (United States)

    Myers, R. Thomas

    1983-01-01

    Discusses the values presented in various handbooks for the boiling point and heat of vaporization of sulfuric acid, noting discrepencies. Analyzes various approaches to data presentation, discussing the data on sulfuric acid in light of the Trouton constant. Points out the need for a more critical use of tables. (JM)

  13. 40 CFR 418.50 - Applicability; description of the nitric acid subcategory.

    Science.gov (United States)

    2010-07-01

    ... are applicable to discharges resulting from production of nitric acid in concentrations up to 68... nitric acid subcategory. 418.50 Section 418.50 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) EFFLUENT GUIDELINES AND STANDARDS FERTILIZER MANUFACTURING POINT SOURCE CATEGORY Nitric...

  14. Separation of Rare Earth Concentrate from Nitric Acid and Sulphuric Acid in Fertilizers production Processing

    International Nuclear Information System (INIS)

    Different processes were proposed and applied for the treatment of a phosphate rocks for the recovery of the rare earth concentrate (REC). The processes assure the production of phosphatic fertilizers without polluting the environment with traces radioactive materials. Two individual systems were utilized for the recovery of REC using nitric acid and sulphuric acid as leaching agents. In nitric acid about 90% of the REC pass into the phosphoric acid solution and was precipitated by neutralization with ammonia up to ph 1.8±0.1. In the sulphuric acid the REC extraction is about 60%. Sulphuric acid is preferred economically where the use of nitric acid needs purification processes from nitrate anions. A mixed method based on each one was investigated to get a more economical recovery

  15. Changes in the phenolic acid content during wort boiling and whirlpool

    Directory of Open Access Journals (Sweden)

    Dominik Szwajgier

    2011-03-01

    Full Text Available Background. Phenolic acids were repeatedly pointed out as powerful antioxidants. The studies in the past prove the differences in the phenolic acids content in malts and worts. In this work, the influence of wort boiling and whirlpool separation on the phenolic acid content was studied. Material and methods. Worts were produced in the local brewery by the infusion method using pale pilsner-type barley malt. Samples were analysed at the beginning of the boil, after the boil and after whirlpool separation (5 and 30 min. Free and total alkali extractable phenolic acids contents were analysed using HPLC-DAD. Results. The main phenolic acid in all worts was ferulic acid in the free (35.47 ±3.28-117.51 ±4.40 mg·dm-3 as well as total alkali extractable form (193.49 ±4.84-294.72 ±2.65 mg·dm-3. With both forms no decrease was seen after boiling of wort (80 min at 100-100.5°C followed by wort separation in the whirlpool. Similarly, no significant changes in the free and total form of p-coumaric acid content were seen. Conclusions. It can be concluded that an elevated temperature during wort boiling and separation in whirlpool had no significant influence on the content of phenolic acids (at least in the case of the specific mashing program applied in this brewery: equipment, enzyme preparations, mashing, time-temperature parameters etc.. The differences in the phenolic acids levels could be rather attributed to different supplies of malt used for the production.

  16. Omega-3 fatty acids improve psychomotor performance via mechanism not related to nitric acid production

    OpenAIRE

    Al-Nimer, Marwan S M; Ali I Al-Gareeb; Hayder M. Al-kuraishy

    2012-01-01

    Omega-3 fatty acids (ω-3FAs) are essential polyunsaturated fats that protect the brain from cognitive impairment. It increases the activity of endothelial nitric oxide synthetase (eNOS) and thereby increases the nitric acid (NO) production. This study aimed to explore the effect of ω-3FAs on psychomotor performance and to relate this effect to the reactive nitrogen species. This study was conducted in Department of Pharmacology, College of Medicine, Al-Mustansiriya University in Baghdad, Iraq...

  17. Extraction behavior of cerium by tetraoctyldiglycolamide from nitric acid solutions

    International Nuclear Information System (INIS)

    The diamide N,N,N',N'-tetraoctyldiglycolamide (TODGA) was synthesized and characterized. The prepared TODGA was applied for extraction of Ce(III) from nitric acid solutions. The equilibrium studies included the dependencies of cerium distribution ratio on nitric acid, TODGA, nitrate ion, hydrogen ion and cerous ion concentrations. Analysis of the results indicates that the main extracted species is Ce(TODGA)2(NO3)3HNO3. The capacity of Ce loading is approximately 45 mmol/L for 0.1 M solution of TODGA in n-hexane. Finally, the thermodynamic parameters were calculated: K (25 deg C) = 3.8 x 103, ΔH = -36.7 ± 1.0 kJ/mol, ΔS = -54.6 ± 3.0 J/K mol, and ΔG = -20.4 ± 0.1 kJ/mol. (author)

  18. Removal of iodine species by concentrated nitric acid, (5)

    International Nuclear Information System (INIS)

    In the reprocessing of FBR spent fuel, it is important to retain radioiodine inside the process. The trapping of the iodine in hyperazeotropic nitric acid is promising to retain radioiodine (Iodox process). Considerable amount of nitrogen oxides is contained in the off-gas. The effects of NO2 on the trapping of methyl iodide are described. (1) The nitrite concentration in nitric acid is easily reduced to less than 10-3 mol/l by aeration, and after this operation, higher decontamination factor DF is expected. (2) NO2 in gas phase reduces the DF significantly even at the concentration as low as 0.5 vol. %. (3) Capacity coefficient is independent of the flow rate of liquid, it increases as the flow rate of gas increases in 19.8 N HNO3, but it does not increase at 18.5 N. (J.P.N.)

  19. UV Photodissociation Dynamics of Nitric Acid: The Hydroxyl Elimination Channel

    Institute of Scientific and Technical Information of China (English)

    Fengyan Wang; Zhichao Chen; Yongwei Zhang; Quan Shuai; Bo Jiang; Dongxu Dai; Xiuyan Wang; Xueming Yang

    2009-01-01

    Sliced velocity mapping ion imaging technique was employed to investigate the dynamics of the hydroxyl elimination channel in the photodissociaiton of nitric acid in the ultraviolet region. The OH product was detected by (2+1) resonance enhanced multiphoton ionization via the D2∑- electronic state. The total kinetic energy spectra of the OH+NO2 channel from the photolysis of HONO2 show that both NO2(X2A1) and NO2 (A2B2) channels are present,suggesting that both 11A" and 21A" excited electronic states of HONO2 are involved in the excitation. The parallel angular distributions suggest that the dissociation of the nitric acid is a fast process in comparison with the rotational period of the HNO3 molecule. The anisotropy parameter β for the hydroxyl elimination channel is found to be dependent on the OH product rotational state as well as the photolysis energy.

  20. Energy integration of nitric acid production using pinch methodology

    OpenAIRE

    Ivaniš Gorica R.; Lazarević Marija; Radović Ivona R.; Kijevčanin Mirjana Lj.

    2015-01-01

    Pinch methodology was applied to the heat exchangers network (HEN) synthesis of nitric acid production. The integration is analyzed in two ways, and the results are presented as two different solutions: (i) the first solution is based on the original heat transfer equipment arrangement, (ii) in order to eliminate the shortages of the first solution the second HEN was obtained using process simulation with optimized process parameters. Optimized HEN, with ne...

  1. Stainless steels with low contents in residual elements for nitric acid environments. Influence of melting processes

    International Nuclear Information System (INIS)

    Nitric acid solutions, as they are for instance employed in the chemical treatment of nuclear fuels, do not apparently pose any more corrosion problems and the safe use of the several steels is well documented. The most difficult corrosion problems are next those related to ''tunnel'' penetrations, in the hot-rolling direction (longitudinal). This phenomenon can be quite important such as to imperial complex structures. Up to the last few years, the only manner to eliminate such ''tunnel'' corrosions was to carry out special operations of remelting and refining under careful selected slag (Electro Slag Remelting or ESR). It turns out indeed that non metallic inclusions are the prime factors in this type of corrosion. Well adapted ladle refining processes made possible to obtain equivalent results at lower costs, while purity and cleanliness are improved to such a degree that a steel of type Cr 18 - Ni 10 thus produced exhibit a nearly absolute resistance to intergranular corrosion in the 14 N (65%) boiling nitric acid (the Huey test) whatever the ''sensitization'' treatment, between 10000C and 6000C. In view of its very high tolerance to varied thermal cycles and of the near complete disappearance of any ''tunnel'' corrosion, such a steel is of great interest when complex parts are produced, by machining forged or rolled metal, which is then assembled by welding techniques or procedures which would be forbidden in the case of usual Cr 18 -Ni 10 steels. Similar improvements are also obtained on the two other special steels used in nitric environments: Cr 25 - Ni 20 - C <= 0,020 (Nb) and Cr 17 - Ni 14 - Si 4 - C <= 0,015 (Nb)

  2. The photochemistry of neptunium in aqueous nitric acid solutions

    International Nuclear Information System (INIS)

    Photochemical reactions of Np(IV), (V) and (VI) have been investigated in nitric acid solutions using 254 and 300 nm excitation from standard mercury discharge lamps. Absorption spectrometry was used to monitor the concentrations of the various neptunium species in solution. In the absence of added reagents, all oxidation states of neptunium are converted to the pentavalent state. The effect of adding urea and mild reducing agents such as ethanol and hydrazine on the photolysis has also been examined. Quantum efficiencies for these reactions have been found to vary from 0.001 to 0.1, depending on the acid concentration, wavelength, and reaction conditions. (orig.)

  3. Stress corrosion cracking of zirconium in nitric acid

    International Nuclear Information System (INIS)

    The susceptibility of zirconium and its common alloys to stress corrosion cracking (SCC) in nitric acid was investigated by slow strain-rate and constant deflection techniques. Cracking occurred at 250C over a wide range of acid concentrations and electrochemical potentials. The crack velocity increased slightly with increasing temperature. The failure mode was transgranular and the morphology was similar to SCC failures of zirconium alloys in other environments. The fracture was very orientation-dependent suggesting that it occurs on a single crystallographic plane in the material. The results of the study are not consistent with a hydrogen mechanism for cracking

  4. The influence of nitric acid on the cloud processing of aerosol particles

    OpenAIRE

    Romakkaniemi, S.; Kokkola, H.; Lehtinen, K.E.J.; Laaksonen, A

    2005-01-01

    In this paper we present simulations of the effect of nitric acid (HNO3) on cloud processing of aerosol particles. Sulfuric acid (H2SO4) production and incloud coagulation are both affected by condensed nitric acid as nitric acid increases the number of cloud droplets, which will lead to smaller mean size and higher total surface area of droplets. As a result of increased cloud droplet number concentration (CDNC), the incloud coagulation rate is enhanced by a factor of 1...

  5. Alternative to Nitric Acid for Passivation of Stainless Steel Alloys

    Science.gov (United States)

    Lewis, Pattie L.; Kolody, Mark; Curran, Jerry

    2013-01-01

    Corrosion is an extensive problem that affects the Department of Defense (DoD) and National Aeronautics and Space Administration (NASA). The deleterious effects of corrosion result in steep costs, asset downtime affecting mission readiness, and safety risks to personnel. Consequently, it is vital to reduce corrosion costs and risks in a sustainable manner. The DoD and NASA have numerous structures and equipment that are fabricated from stainless steel. The standard practice for protection of stainless steel is a process called passivation. Typical passivation procedures call for the use of nitric acid; however, there are a number of environmental, worker safety, and operational issues associated with its use. Citric acid offers a variety of benefits including increased safety for personnel, reduced environmental impact, and reduced operational cost. DoD and NASA agreed to collaborate to validate citric acid as an acceptable passivating agent for stainless steel. This paper details our investigation of prior work developing the citric acid passivation process, development of the test plan, optimization of the process for specific stainless steel alloys, ongoing and planned testing to elucidate the process' resistance to corrosion in comparison to nitric acid, and preliminary results.

  6. Metals for the containment of nitric acid solutions of plutonium-238

    International Nuclear Information System (INIS)

    Results of a study of the corrosion of various transition-metal alloys, tantalum, and tantalum/2.5% tungsten are reported. The solvent contained nitric acid, hydrofluoric acid, and ammonium hexanitratocerate. It was designed to imitate the corrosiveness of the nitric acid, hydrofluoric acid mixture used to dissolve 238-plutonium dioxide. (author)

  7. Reduction Rates for Higher Americium Oxidation States in Nitric Acid

    Energy Technology Data Exchange (ETDEWEB)

    Grimes, Travis Shane [Idaho National Lab. (INL), Idaho Falls, ID (United States); Mincher, Bruce Jay [Idaho National Lab. (INL), Idaho Falls, ID (United States); Schmitt, Nicholas C [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2015-09-30

    The stability of hexavalent americium was measured using multiple americium concentrations and nitric acid concentrations after contact with the strong oxidant sodium bismuthate. Contrary to our hypotheses Am(VI) was not reduced faster at higher americium concentrations, and the reduction was only zero-order at short time scales. Attempts to model the reduction kinetics using zero order kinetic models showed Am(VI) reduction in nitric acid is more complex than the autoreduction processes reported by others in perchloric acid. The classical zero-order reduction of Am(VI) was found here only for short times on the order of a few hours. We did show that the rate of Am(V) production was less than the rate of Am(VI) reduction, indicating that some Am(VI) undergoes two electron-reduction to Am(IV). We also monitored the Am(VI) reduction in contact with the organic diluent dodecane. A direct comparison of these results with those in the absence of the organic diluent showed the reduction rates for Am(VI) were not statistically different for both systems. Additional americium oxidations conducted in the presence of Ce(IV)/Ce(III) ions showed that Am(VI) is reduced without the typical growth of Am(V) observed in the systems sans Ce ion. This was an interesting result which suggests a potential new reduction/oxidation pathway for Am in the presence of Ce; however, these results were very preliminary, and will require additional experiments to understand the mechanism by which this occurs. Overall, these studies have shown that hexavalent americium is fundamentally stable enough in nitric acid to run a separations process. However, the complicated nature of the reduction pathways based on the system components is far from being rigorously understood.

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

    Energy Technology Data Exchange (ETDEWEB)

    Hyder, M.L

    1994-01-01

    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.

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

    International Nuclear Information System (INIS)

    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

  10. Experimental study on thermal hazard of tributyl phosphate-nitric acid mixtures using micro calorimeter technique.

    Science.gov (United States)

    Sun, Qi; Jiang, Lin; Gong, Liang; Sun, Jin-Hua

    2016-08-15

    During PUREX spent nuclear fuel reprocessing, mixture of tributyl phosphate (TBP) and hydrocarbon solvent are employed as organic solvent to extract uranium in consideration of radiation contaminated safety and resource recycling, meanwhile nitric acid is utilized to dissolve the spent fuel into small pieces. However, once TBP contacts with nitric acid or nitrates above 130°C, a heavy "red oil" layer would occur accompanied by thermal runaway reactions, even caused several nuclear safety accident. Considering nitric acid volatility and weak exothermic detection, C80micro calorimeter technique was used in this study to investigate thermal decomposition of TBP mixed with nitric acid. Results show that the concentration of nitric acid greatly influences thermal hazard of the system by direct reactions. Even with a low heating rate, if the concentration of nitric acid increases due to evaporation of water or improper operations, thermal runaway in the closed system could start at a low temperature. PMID:27136728

  11. Optimization of conditions to produce nitrous gases by electrochemical reduction of nitric acid

    International Nuclear Information System (INIS)

    Gaseous nitrogen oxides (NO and NO2) involved as oxidizing agents in nuclear fuel reprocessing can be an produced by electrochemical reduction of nitric acid. This could be an interesting alternative to the usual process because no wastes are generated. Voltammetric studies on a platinum electrode show that two reduction potential regions are observed in concentrated nitric acid solutions, between 0.05 VSHE and 0.3 VSHE and O.5 VSHE and 1 VSHE. The highest potential region reduction mechanism was studies by: classical micro-electrolysis methods; macro-electrolysis methods; infra-red spectroscopy couplet to electrochemistry. It was determined that the origin of nitric acid reduction is the electrochemical reduction of nitrous acid in nitric oxide which chemically reduces nitric acid. This reaction produces nitrous acid back which indicate an auto-catalytic behaviour of nitric acid reduction mechanism. Nitrogen dioxide evolution during nitric acid reduction can also be explained by an other chemical reaction. In the potential value of platinum electrode is above 0.8 VSHE, products of the indirect nitric acid reduction are nitrous acid, nitrogen oxide and nitrogen dioxide. Below this value nitric oxide can be reduced in nitrous oxide. Thus the potential value is the most important parameter for the nitrogen oxides production selectivity. However, owing to the auto-catalytic character of the reduction mechanism, potential value can be controlled during intentiostatic industrial electrolysis. (author)

  12. Simultaneous Measurement of Nitrous Acid,Nitric Acid, and Nitrogen Dioxide by Means \

    Czech Academy of Sciences Publication Activity Database

    Vichi, F.; Mašková, Ludmila; Frattoni, M.; Imperiali, A.; Smolík, Jiří

    2016-01-01

    Roč. 4, FEB 22 (2016), s. 4. ISSN 2050-7445. [International Conference on Indoor Air Quality in Heritage and Historic Environments /11./. Prague, 13.04.2014-16.04.2014] Institutional support: RVO:67985858 Keywords : diffusive sampling * nitrous acid * nitric acid Subject RIV: CF - Physical ; Theoretical Chemistry

  13. Study of iodine recovery with platinum-active carbon from nitric acid solution

    International Nuclear Information System (INIS)

    Platinum-Active Carbon (Pt-C) was synthesized and its adsorption and desorption properties in low acidity nitric solution were discussed. It showed that Pt-C can absorb I- and IO3- with high exchange capacity in nitric acid solution, and the recovery rate of I-and IO3- is more than 90%, thus Pt-C can be used for iodine recovery in low acidity nitric solution. (authors)

  14. Recovery of plutonium from nitric-acid waste streams

    International Nuclear Information System (INIS)

    Nitric acid (7M) waste streams at Rocky Flats contain 0.01 to 0.001 g/1 plutonium and new processes are under development to reduce the plutonium levels to 10-5 g/1. Anion exchange and solvent extraction methods are under evaluation. Several macroreticular and microreticular anion exchange resins were evaluated and Rohm and Hass (IRA-938) gave significant improvement in plutonium capacity and elution over several other resins tested. The solvent extraction process uses dihexyl-N, N-diethylcarbamylmethylene phosphonate extractant. The results of recent tests using a combined anion exchange extraction chromatography process will be described for recovering both plutonium and americum

  15. Energy integration of nitric acid production using pinch methodology

    Directory of Open Access Journals (Sweden)

    Ivaniš Gorica R.

    2015-01-01

    Full Text Available Pinch methodology was applied to the heat exchangers network (HEN synthesis of nitric acid production. The integration is analyzed in two ways, and the results are presented as two different solutions: (i the first solution is based on the original heat transfer equipment arrangement, (ii in order to eliminate the shortages of the first solution the second HEN was obtained using process simulation with optimized process parameters. Optimized HEN, with new arrangement of heat exchangers, gave good results in energy and process optimization. [Projekat Ministarstva nauke Republike Srbije, br. P172063

  16. Investigation of products of molybdenite oxidation by nitric acid

    International Nuclear Information System (INIS)

    Physicochemical study of products of oxidation by nitric acid of molybdenum concentrate containing 98% MoS2 is carried out. It is shown that appearing molybdenum oxide forms block oxidizer access to the surface of sulfide phase and hinder its complete oxidation. When complexing reagents (H2SO4, H3PO4, HCl) are introduced in the solution the bulk of oxidized molybdenum transfers into solution in the form of a stable complex, at that. The effect of internal diffusion decreases and a considerable increase of MoS2 oxidation rate and completeness is achieved

  17. Optimization of the nitrous vapors experimental conditions production by nitric acid electrochemical reduction

    International Nuclear Information System (INIS)

    Gaseous nitrogen oxides (NO and NO2) involved as oxidizing agents in nuclear fuel reprocessing can be produced by electrochemical reduction of nitric acid. This is an interesting alternative to the existing process because no wastes are generated. voltammetric studies on a platinum electrode show that two reduction potential regions are observed in concentrated nitric acid solutions, between 0,05 VSHE and between 0,5 VSHE and 1 VSHE. The highest potential region reduction mechanism was studied by: classical micro-electrolysis methods, macro-electrolysis methods, infrared spectroscopy coupled to electrochemistry. It was determined that the origin of nitric acid reduction is the electrochemical reduction of nitrous acid in nitric oxide which chemically reduces nitric acid. This reaction produces nitrous acid back which indicate an auto-catalytic behaviour of nitric acid reduction mechanism. Nitrogen dioxide evolution during nitric reduction can also explained by an other chemical reaction. If the potential value of platinum electrode is above 0,8 VSHE, products of the indirect nitric acid reduction are nitrous acid, nitrogen oxide and nitrogen dioxide. Below this value nitric oxide can be reduced in nitrous oxide. Thus the potential value is the most important parameter for the nitrogen oxides production selectivity. However, owing to the auto-catalytic character of the reduction mechanism, potential value can be controlled during intentiostatic industrial electrolysis. (author)

  18. Nitrosation and Nitration of Fulvic Acid, Peat and Coal with Nitric Acid

    Science.gov (United States)

    Thorn, Kevin A.; Cox, Larry G.

    2016-01-01

    Nitrohumic acids, produced from base extraction of coals and peats oxidized with nitric acid, have received considerable attention as soil ammendments in agriculture. The nitration chemistry however is incompletely understood. Moreover, there is a need to understand the reaction of nitric acid with natural organic matter (NOM) in general, in the context of a variety of environmental and biogeochemical processes. Suwannee River NOM, Suwannee River fulvic acid, and Pahokee Peat fulvic acid were treated with 15N-labeled nitric acid at concentrations ranging from 15% to 22% and analyzed by liquid and solid state 15N NMR spectroscopy. Bulk Pahokee peat and Illinois #6 coal were also treated with nitric acid, at 29% and 40% respectively, and analyzed by solid state 15N NMR spectroscopy. In addition to nitro groups from nitration of aromatic carbon, the 15N NMR spectra of all five samples exhibited peaks attributable to nitrosation reactions. These include nitrosophenol peaks in the peat fulvic acid and Suwannee River samples, from nitrosation of phenolic rings, and N-nitroso groups in the peat samples, from nitrosation of secondary amides or amines, the latter consistent with the peat samples having the highest naturally abundant nitrogen contents. Peaks attributable to Beckmann and secondary reactions of the initially formed oximes were present in all spectra, including primary amide, secondary amide, lactam, and nitrile nitrogens. The degree of secondary reaction product formation resulting from nitrosation reactions appeared to correlate inversely with the 13C aromaticities of the samples. The nitrosation reactions are most plausibly effected by nitrous acid formed from the reduction of nitric acid by oxidizable substrates in the NOM and coal samples. PMID:27175784

  19. Nitrosation and nitration of fulvic acid, peat and coal with nitric acid

    Science.gov (United States)

    Thorn, Kevin A.; Cox, Larry G.

    2016-01-01

    Nitrohumic acids, produced from base extraction of coals and peats oxidized with nitric acid, have received considerable attention as soil ammendments in agriculture. The nitration chemistry however is incompletely understood. Moreover, there is a need to understand the reaction of nitric acid with natural organic matter (NOM) in general, in the context of a variety of environmental and biogeochemical processes. Suwannee River NOM, Suwannee River fulvic acid, and Pahokee Peat fulvic acid were treated with 15N-labeled nitric acid at concentrations ranging from 15% to 22% and analyzed by liquid and solid state 15N NMR spectroscopy. Bulk Pahokee peat and Illinois #6 coal were also treated with nitric acid, at 29% and 40% respectively, and analyzed by solid state 15N NMR spectroscopy. In addition to nitro groups from nitration of aromatic carbon, the 15N NMR spectra of all five samples exhibited peaks attributable to nitrosation reactions. These include nitrosophenol peaks in the peat fulvic acid and Suwannee River samples, from nitrosation of phenolic rings, and N-nitroso groups in the peat samples, from nitrosation of secondary amides or amines, the latter consistent with the peat samples having the highest naturally abundant nitrogen contents. Peaks attributable to Beckmann and secondary reactions of the initially formed oximes were present in all spectra, including primary amide, secondary amide, lactam, and nitrile nitrogens. The degree of secondary reaction product formation resulting from nitrosation reactions appeared to correlate inversely with the 13C aromaticities of the samples. The nitrosation reactions are most plausibly effected by nitrous acid formed from the reduction of nitric acid by oxidizable substrates in the NOM and coal samples.

  20. Effect of soluble additives, boric acid (H3BO3) and salt (NaCI), in pool boiling heat transfer

    International Nuclear Information System (INIS)

    The effects on pool boiling heat transfer of aqueous solutions of boric acid (H3BO3) and sodium chloride (NaCl) as working fluids have been studied. Borated and NaCl water were prepared by dissolving 0.5∼5% volume concentration of boric acid and NaCl in distilled-deionized water. The pool boiling tests were conducted using 1 x 1 cm2 flat heaters at 1 atm. The critical heat flux (CHF) dramatically increased compared to boiling pure water. At the end of boiling tests it was observed that particles of boric acid and NaCl had deposited and formed a coating on the heater surface. The CHF enhancement and surface modification during boiling tests were very similar to those obtained from boiling with nanofluids. Additional experiments were carried out to investigate the reliability of the additives deposition in pure water. The boric acid and NaCl coatings disappeared after repeated boiling tests on the same surface due to the soluble nature of the coatings, thus CHF enhancement no longer existed. These results demonstrate that not only insoluble nanoparticles but also soluble salts can be deposited during boiling process and the deposited layer is solely responsible for significant CHF enhancement

  1. Impact of scaling on the nitric-glycolic acid flowsheet

    Energy Technology Data Exchange (ETDEWEB)

    Lambert, D. [Savannah River Site (SRS), Aiken, SC (United States)

    2016-02-01

    Savannah River Remediation (SRR) is considering using glycolic acid as a replacement for formic acid in Sludge Receipt and Adjustment Tank (SRAT) processing in the Defense Waste Processing Facility (DWPF). Catalytic decomposition of formic acid is responsible for the generation of hydrogen, a potentially flammable gas, during processing. To prevent the formation of a flammable mixture in the offgas, an air purge is used to dilute the hydrogen concentration below the 60% of the Composite Lower Flammability Limit (CLFL). The offgas is continuously monitored for hydrogen using Gas Chromatographs (GCs). Since formic acid is much more volatile and toxic than glycolic acid, a formic acid spill would lead to the release of much larger quantities to the environment. Switching from formic acid to glycolic acid is expected to eliminate the hydrogen flammability hazard leading to lower air purges, thus downgrading of Safety Significant GCs to Process Support GCs, and minimizing the consequence of a glycolic acid tank leak in DWPF. Overall this leads to a reduction in process operation costs and an increase in safety margin. Experiments were completed at three different scales to demonstrate that the nitric-glycolic acid flowsheet scales from the 4-L lab scale to the 22-L bench scale and 220-L engineering scale. Ten process demonstrations of the sludge-only flowsheet for SRAT and Slurry Mix Evaporator (SME) cycles were performed using Sludge Batch 8 (SB8)-Tank 40 simulant. No Actinide Removal Process (ARP) product or strip effluent was added during the runs. Six experiments were completed at the 4-L scale, two experiments were completed at the 22-L scale, and two experiments were completed at the 220-L scale. Experiments completed at the 4-L scale (100 and 110% acid stoichiometry) were repeated at the 22-L and 220-L scale for scale comparisons.

  2. Impact of scaling on the nitric-glycolic acid flowsheet

    International Nuclear Information System (INIS)

    Savannah River Remediation (SRR) is considering using glycolic acid as a replacement for formic acid in Sludge Receipt and Adjustment Tank (SRAT) processing in the Defense Waste Processing Facility (DWPF). Catalytic decomposition of formic acid is responsible for the generation of hydrogen, a potentially flammable gas, during processing. To prevent the formation of a flammable mixture in the offgas, an air purge is used to dilute the hydrogen concentration below the 60% of the Composite Lower Flammability Limit (CLFL). The offgas is continuously monitored for hydrogen using Gas Chromatographs (GCs). Since formic acid is much more volatile and toxic than glycolic acid, a formic acid spill would lead to the release of much larger quantities to the environment. Switching from formic acid to glycolic acid is expected to eliminate the hydrogen flammability hazard leading to lower air purges, thus downgrading of Safety Significant GCs to Process Support GCs, and minimizing the consequence of a glycolic acid tank leak in DWPF. Overall this leads to a reduction in process operation costs and an increase in safety margin. Experiments were completed at three different scales to demonstrate that the nitric-glycolic acid flowsheet scales from the 4-L lab scale to the 22-L bench scale and 220-L engineering scale. Ten process demonstrations of the sludge-only flowsheet for SRAT and Slurry Mix Evaporator (SME) cycles were performed using Sludge Batch 8 (SB8)-Tank 40 simulant. No Actinide Removal Process (ARP) product or strip effluent was added during the runs. Six experiments were completed at the 4-L scale, two experiments were completed at the 22-L scale, and two experiments were completed at the 220-L scale. Experiments completed at the 4-L scale (100 and 110% acid stoichiometry) were repeated at the 22-L and 220-L scale for scale comparisons.

  3. Chemistry of tributyl phosphate and nitric acid at constant volume

    International Nuclear Information System (INIS)

    This paper addresses the reaction of tributyl phosphate (TBP) with nitric acid (HNO3). The reaction pressure of TBP/HNO3 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

  4. Corrosion investigations on zircaloy-4 and titanium dissolver materials for MOX fuel dissolution in concentrated nitric acid containing fluoride ions

    Science.gov (United States)

    Jayaraj, J.; Krishnaveni, P.; Krishna, D. Nanda Gopala; Mallika, C.; Mudali, U. Kamachi

    2016-05-01

    Aqueous reprocessing of plutonium-rich mixed oxide fuels require fluoride as a dissolution catalyst in boiling nitric acid for an effective dissolution of the spent fuel. High corrosion rates were obtained for the candidate dissolver materials zircaloy-4 (Zr-4) and commercial pure titanium (CP-Ti grade 2) in boiling 11.5 M HNO3 + 0.05 M NaF. Complexing the fluoride ions either with Al(NO3)3 or ZrO(NO3)2 aided in decreasing the corrosion rates of Zr-4 and CP-Ti. From the obtained corrosion rates it is concluded that CP-Ti is a better dissolver material than Zr-4 for extended service life in boiling 11.5 M HNO3 + 0.05 M NaF, when complexed with 0.15 M ZrO(NO3)2. XPS analysis confirmed the presence of TiO2 and absence of fluoride on the surface of CP-Ti samples, indicating that effective complexation had occurred in solution leading to passivation of the metal and imparting high corrosion resistance.

  5. REE and TPE sorption on strong-acid sulfocation exchanger KU-2 from nitric acid solutions

    International Nuclear Information System (INIS)

    Sorption of rare earths on strong acid sulfocationite KU-2, depending on solution acidity (0.1-2.0 mol/l nitric acid) and rare earths concentration, has been studied. It is ascertained that in solutions concentrated in terms of nitrate-ions, where formation of M(NO3)2+ and M(NO3)2+ complexes is possible, a seeming increase in the ionite capacity by approximately 20% is observed. 3 refs.; 1 fig.; 5 tabs

  6. Flotation extraction of actinoids and lanthanoids from nitric acid solutions

    International Nuclear Information System (INIS)

    A study was made on possibility of using method of ion flotation for extraction of actinoids and lanthanoids from liquid radioactive wastes of spent fuel reprocessing. For this purpose ion flotation of thorium, plutonium (4), uranium (6) and gadolinium from aqueous nitric acid solutions (HNO3 concentration - from 0.01 up to 5.0 mol/l) was investigated, using lauryl phosphoric acid (LPA) as surfactant-collector. Growth of the degree of separation of metal ions with increase of LPA, introduced into the system, independently of acidity of solutions was established. Decrease of separation degree of uranium (6) and gadolinium with acidity growth and constancy of this parameter for plutonium (4) and thorium are observed at fixed mole LPA/metal ratio. Principle possibility of 100% flotation extraction of plutonium (4) and thorium independently of acidity of aqueous solutions is shown. Addition of 0.5 mol/l Ca(NO3)2 into the system doesn't produce sufficient effect on flotation extraction of thorium

  7. Delayed effects of inhaled nitric acid aerosols in the rat: preliminary studies

    International Nuclear Information System (INIS)

    Rats that inhaled transuranic nitrate aerosols in a toxicology study were simultaneously exposed to aerosols of the suspending solution, nitric acid. Results indicated that exposure to nitric acid was associated with the finding of bone tumors. Other rats, exposed to low levels of inhaled Pu(NO3)4, showed one osteosarcoma in 79 rats examined

  8. Research on the Stability of Dimethyl Hydroxylamine-methyl Hydrazinein Nitric Acid Medium

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    By the means of the comparison of the extraction of PU(Ⅲ) and plutonium in nitric acid mediumcontaining dimethyl hydroxylamine-methyl hydrazine and the analysis of the percent content of PU(Ⅳ) inthe system, the stability of dimethyl hydroxylamine-methyl hydrazine in nitric acid medium is

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

    International Nuclear Information System (INIS)

    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

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

    Energy Technology Data Exchange (ETDEWEB)

    Green, J.R.

    1995-05-16

    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.

  11. Airborne measurements of the nitric acid partitioning in persistent contrails

    Directory of Open Access Journals (Sweden)

    Th. Peter

    2009-11-01

    Full Text Available This study reports the first systematic measurements of nitric acid (HNO3 uptake in contrail ice particles at typical aircraft cruise altitudes. During the CIRRUS-III campaign cirrus clouds and almost 40 persistent contrails were probed with in situ instruments over Germany and Northern Europe in November 2006. Besides reactive nitrogen, water vapor, cloud ice water content, ice particle size distributions, and condensation nuclei were measured during 6 flights. Contrails with ages up to 12 h were detected at altitudes 10–11.5 km and temperatures 211–220 K. These contrails had a larger ice phase fraction of total nitric acid (HNO3ice/HNO3tot = 6% than the ambient cirrus layers (3%. On average, the contrails contained twice as much HNO3ice as the cirrus clouds, 14 pmol/mol and 6 pmol/mol, respectively. Young contrails with ages below 1 h had a mean HNO3ice of 21 pmol/mol. The contrails had higher nitric acid to water molar ratios in ice and slightly higher ice water contents than the cirrus clouds under similar meteorological conditions. The differences in ice phase fractions and molar ratios between developing contrails and cirrus are likely caused by high plume concentrations of HNO3 prior to contrail formation. The location of the measurements in the upper region of frontal cirrus layers might account for slight differences in the ice water content between contrails and adjacent cirrus clouds. The observed dependence of molar ratios as a function of the mean ice particle diameter suggests that ice-bound HNO3 concentrations are controlled by uptake of exhaust HNO3 in the freezing plume aerosols in young contrails and subsequent trapping of ambient HNO3 in growing ice particles in older (age > 1 h contrails.

  12. Airborne measurements of the nitric acid partitioning in persistent contrails

    Directory of Open Access Journals (Sweden)

    D. Schäuble

    2009-06-01

    Full Text Available This study reports the first systematic measurements of nitric acid (HNO3 uptake in contrail ice particles at typical aircraft cruise altitudes. During the CIRRUS-III campaign cirrus clouds and almost 40 persistent contrails were probed with in situ instruments over Germany and Northern Europe in November 2006. Besides reactive nitrogen, water vapor, cloud ice water content, ice particle size distributions, and condensation nuclei were measured during 6 flights. Contrails with ages up to 8 hours were detected at altitudes 10–11.5 km and temperatures 211–220 K. These contrails had a larger ice phase fraction of total nitric acid (HNO3ice/HNO3tot = 6% than the ambient cirrus layers (3%. On average, the contrails contained twice as much HNO3ice as the cirrus clouds, 14 pmol/mol and 6 pmol/mol, respectively. Young contrails with ages below 1 h had a mean HNO3ice of 21 pmol/mol. The contrails had higher nitric acid to water molar ratios in ice and slightly higher ice water contents than the cirrus clouds under similar meteorological conditions. The differences in ice phase fractions and molar ratios between developing contrails and cirrus are likely caused by high plume concentrations of HNO3 prior to contrail formation. The location of the measurements in the top region of frontal cirrus layers might account for slight differences in the ice water content between contrails and adjacent cirrus clouds. The observed dependence of molar ratios as a function of the mean ice particle diameter suggests that ice-bound HNO3 concentrations are controlled by uptake of exhaust HNO3 in the freezing plume aerosols in young contrails and subsequent trapping of ambient HNO3 in growing ice particles in older (age > 1 h contrails.

  13. Extraction of uranium from nitric acid solutions by tributylphosphate/kerosene

    International Nuclear Information System (INIS)

    The extraction of nitric acid and hexavalent uranium from nitric acid and nitric acid containing uranium(VI) media by tributylphosphate (TBP)/kerosene has been studied, and all factors affecting the extraction process (time of mixing, uranium concentration, nitric acid concentration, TBP concentration, temperature) have been investigated. The equilibrium constant of the extraction reaction of uranium by TBP was found to be 102.464, 102.668 L4/mol4 at 25 C, and the enthalpy was -16.47, -23.07 k.J/mol for 0.5 M and 1 M nitric acid concentration respectively. The optimal conditions obtained from this study were applied on the purification of the Yellow cake resulted as a byproduct from the Pilot Plant of H3PO4 purification in the TSP fertilizer company in Homs. (Authors)

  14. Method of separating multi-ingredient mixed nitric acid solution

    International Nuclear Information System (INIS)

    A multi-ingredient mixed nitric acid solution as high level liquid wastes is heated to a temperature higher than the denitrification temperature at which transuranium elements are converted from the form of nitrate compounds to oxides, and then water is added. The transuranium elements are converted into water insoluble oxides. On the contrary, since nuclides of fission products having extremely high denitrification temperatures are left in the form of nitrates as they are even after the heating and they are dissolved in water, only the transuranium elements can be easily separated. The solution selectively separated and removed only with the transuranium elements having long half decay times are vitrified by a usual method. Accordingly, the storage period of the vitrification products is extremely shortened, to improve the processing safety. (T.M.)

  15. Integrating nitric oxide into salicylic acid and jasmonic acid/ ethylene plant defense pathways

    OpenAIRE

    Mur, Luis A. J.; Prats, Elena; Pierre, Sandra; Hall, Michael A.; Hebelstrup, Kim H

    2013-01-01

    Plant defense against pests and pathogens is known to be conferred by either salicylic acid (SA) or jasmonic acid (JA)/ethylene (ET) pathways, depending on infection or herbivore-grazing strategy. It is well attested that SA and JA/ET pathways are mutually antagonistic allowing defense responses to be tailored to particular biotic stresses. Nitric oxide (NO) has emerged as a major signal influencing resistance mediated by both signaling pathways but no attempt has been made to integrate NO in...

  16. Chemical species of fission product ruthenium in the solution of irradiated uranium dioxide in nitric acid

    International Nuclear Information System (INIS)

    High performance liquid chromatography was applied to separate the ruthenium species in the solution of irradiated uranium dioxide in 1 N nitric acid. The separation column was made of a strongly acidic cation exchanger of sulfonic acid type in a Teflon tube. In order to avoid interconversion of the species during separation, elution of the species was performed by 1 N nitric acid without changing the concentration of nitric acid. With this method, not only cationic species but also anionic and neutral species were separated from each other with good resolution. More than 24 chemical species of ruthenium were separated. The ionic valences of the species were determined from their cation and anion exchange behavior in nitric acid. The main species were four anionic species, six neutral species, seven monovalent cations, three divalent cations and four trivalent cations. The relative abundance of the species was determined as a function of elapsed time from the dissolution of irradiated uranium dioxide. Equilibrium between the species was not established even a half-year after dissolution of the irradiated uranium dioxide in nitric acid solution. The extractabilities of the species were determined for a 100% TBP Tri-n-butyl phosphate)-1N nitric acid system. Four of them, two anionic apcies and two monovalent cations in the nitric acid solution, were extracted appreciably by TBP. (orig.)

  17. Buffer capacities of podzolic and peat gleyic podzolic soils to sulfuric and nitric acids

    Science.gov (United States)

    Kuznetsov, N. B.; Alekseeva, S. A.; Shashkova, G. V.; Dronova, T. Ya.; Sokolova, T. A.

    2007-04-01

    Soil samples from the main genetic horizons of pale podzolic and peat gleyic podzolic soils from the Central Forest Reserve were subjected to a continuous potentiometric titration by sulfuric and nitric acids. The sulfate sorption capacity was determined in soil mineral horizons. The buffer capacity of mineral horizons of both soils to sulfuric acid was found to be higher than that to the nitric acid. This is explained by the sorption of sulfates via the mechanism of ligand exchange with the release of hydroxyl groups from the surfaces of Fe and Al hydroxide particles and edge faces of clay crystallites. The buffer capacity of organic horizons of the pale podzolic soil to sulfuric acid proved to be higher than that to nitric acid; in organic horizons of the peat gleyic podzolic soil, the buffer capacity to sulfuric acid was lower than that to nitric acid. The reasons for this phenomenon have yet to be investigated.

  18. The influence of nitric acid on the cloud processing of aerosol particles

    OpenAIRE

    Romakkaniemi, S.; Kokkola, H.; Lehtinen, K.E.J.; Laaksonen, A

    2006-01-01

    In this paper we present simulations of the effect of nitric acid (HNO3) on cloud processing of aerosol particles. Sulfuric acid (H2SO4) production and incloud coagulation are both affected by condensed nitric acid as nitric acid increases the number of cloud droplets, which will lead to smaller mean size and higher total surface area of droplets. As a result of increased cloud droplet number concentration (CDNC), the incloud coagulation rate is enhanced by a factor of 1–1.3, so that t...

  19. Omega-3 fatty acids improve psychomotor performance via mechanism not related to nitric acid production

    Directory of Open Access Journals (Sweden)

    Marwan S. M. Al-Nimer

    2012-01-01

    Full Text Available Omega-3 fatty acids (ω-3FAs are essential polyunsaturated fats that protect the brain from cognitive impairment. It increases the activity of endothelial nitric oxide synthetase (eNOS and thereby increases the nitric acid (NO production. This study aimed to explore the effect of ω-3FAs on psychomotor performance and to relate this effect to the reactive nitrogen species. This study was conducted in Department of Pharmacology, College of Medicine, Al-Mustansiriya University in Baghdad, Iraq. Twenty healthy subjects, allocated randomly from medical college students, were participated in the single blind clinical trial. Participants were divided into two groups, each of ten subjects to receive either placebo or (ω-3FAs (750 mg single oral dose daily for 5 days. They were asked to perform psychomotor performance before and after 5 days of treatment, and venous blood was obtained for determination of serum nitric oxide (NO and peroxynitrite (ONOO. ω-3FAs treated group was significantly different from placebo-treated group in reducing choice and motor reaction times as well as the critical flicker frequency threshold. The serum levels of NO and ONOO in ω-3FAs-treated group did not significantly differ from placebo-treated group. Short term supplementation of ω-3FAs improves the psychomotor performance in young healthy subjects via a mechanism not related to the production of nitric oxide production. Inflorescence is a panicle few flowered and fruit is a capsule. The data of the results obtained were presented and discussed.

  20. Uptake of nitric acid by sub-micron-sized ice particles

    Science.gov (United States)

    Arora, O. P.; Cziczo, D. J.; Morgan, A. M.; Abbatt, J. P. D.; Niedziela, R. F.

    The uptake of gas phase nitric acid by half-micron-diameter ice crystals has been studied at 230 K by measuring the nitrate content of ice particles which have been exposed to 5 × 10-6 torr of nitric acid in a low temperature flow tube. A cold NaOH-coated denuder is used to distinguish gas-phase nitric acid from adsorbed nitric acid. Ice particle diameters were determined by fitting measured aerosol infrared extinction spectra to spectra calculated via Mie theory, and their number density is measured directly with a CN counter. Under conditions in which the surface is saturated and not all the gas-phase nitric acid adsorbs, the measured uptakes are 1.2 × 1014 molecules/cm² where the surface area is the geometric area of the particles. Within experimental uncertainties, this surface coverage is the same as that measured on thin films of ice formed by freezing liquid water. These results are the first quantitative study of the nitric acid uptake capacity of ice particles, and they provide additional support to the suggestion that ice and snow provide a route for the efficient scavenging of nitric acid from the atmosphere.

  1. Uptake of Gas-Phase Nitric Acid by Water-Ice Surfaces

    Science.gov (United States)

    Ullerstam, M.; Abbatt, J. P.

    2004-05-01

    Nitric acid is a widespread molecule found in the atmosphere. It is mainly removed from the troposphere by wet or dry deposition. In colder regions such as the upper troposphere and tropopause where cirrus clouds are formed nitric acid can also be scavenged by cirrus ice particles. The uptake of gas-phase nitric acid by water-ice films has been re-examined with a coated-wall flow tube coupled to a chemical-ionization mass spectrometer (CIMS) at 228K. Previous flow tube studies of this system have shown little dependence of the uptake over the partial pressure regime studied. In these studies the initial, short-term uptake has been the focus and the long term uptake has not been quantified. In this experimental setup it was possible to study the uptake of nitric acid at lower partial pressures resulting in a more atmospherically appropriate determination of the adsorption isotherm and the long term uptake has also been addressed. Measurement of the initial uptake coefficient representing a lower limit will also be presented. Finally, possible burial of nitric acid into the bulk of the ice during continuous growth of the ice film has been studied. In the atmosphere ice particles will be subject to cycles of evaporation and condensation which could cause the nitric acid to be encapsulated into the particle, especially since the major part of the adsorption has been proven to be irreversible. This could enhance the ice particles capacity of scavenging nitric acid.

  2. Effect of Nitric Acid Concentrations on Synthesis and Stability of Maghemite Nanoparticles Suspension

    Directory of Open Access Journals (Sweden)

    Irwan Nurdin

    2014-01-01

    Full Text Available Maghemite (γ-Fe2O3 nanoparticles have been synthesized using a chemical coprecipitation method at different nitric acid concentrations as an oxidizing agent. Characterization of all samples performed by several techniques including X-ray diffraction (XRD, transmission electron microscopy (TEM, alternating gradient magnetometry (AGM, thermogravimetric analysis (TGA, dynamic light scattering (DLS, and zeta potential. The XRD patterns confirmed that the particles were maghemite. The crystallite size of all samples decreases with the increasing concentration of nitric acid. TEM observation showed that the particles have spherical morphology with narrow particle size distribution. The particles showed superparamagnetic behavior with decreased magnetization values at the increasing concentration of nitric acid. TGA measurement showed that the stability temperature decreases with the increasing concentration of nitric acid. DLS measurement showed that the hydrodynamic particle sizes decrease with the increasing concentration of nitric acid. Zeta potential values show a decrease with the increasing concentration of nitric acid. The increasing concentration of nitric acid in synthesis of maghemite nanoparticles produced smaller size particles, lower magnetization, better thermal stability, and more stable maghemite nanoparticles suspension.

  3. Effect of nitric acid concentrations on synthesis and stability of maghemite nanoparticles suspension.

    Science.gov (United States)

    Nurdin, Irwan; Johan, Mohd Rafie; Yaacob, Iskandar Idris; Ang, Bee Chin

    2014-01-01

    Maghemite (γ-Fe2O3) nanoparticles have been synthesized using a chemical coprecipitation method at different nitric acid concentrations as an oxidizing agent. Characterization of all samples performed by several techniques including X-ray diffraction (XRD), transmission electron microscopy (TEM), alternating gradient magnetometry (AGM), thermogravimetric analysis (TGA), dynamic light scattering (DLS), and zeta potential. The XRD patterns confirmed that the particles were maghemite. The crystallite size of all samples decreases with the increasing concentration of nitric acid. TEM observation showed that the particles have spherical morphology with narrow particle size distribution. The particles showed superparamagnetic behavior with decreased magnetization values at the increasing concentration of nitric acid. TGA measurement showed that the stability temperature decreases with the increasing concentration of nitric acid. DLS measurement showed that the hydrodynamic particle sizes decrease with the increasing concentration of nitric acid. Zeta potential values show a decrease with the increasing concentration of nitric acid. The increasing concentration of nitric acid in synthesis of maghemite nanoparticles produced smaller size particles, lower magnetization, better thermal stability, and more stable maghemite nanoparticles suspension. PMID:24963510

  4. Thermal Hazard Evaluation of Lauroyl Peroxide Mixed with Nitric Acid

    Directory of Open Access Journals (Sweden)

    Chi-Min Shu

    2012-07-01

    Full Text Available Many thermal runaway incidents have been caused by organic peroxides due to the peroxy group, –O–O–, which is essentially unstable and active. Lauroyl peroxide (LPO is also sensitive to thermal sources and is incompatible with many materials, such as acids, bases, metals, and ions. From the thermal decomposition reaction of various concentrations of nitric acid (HNO3 (from lower to higher concentrations with LPO, experimental data were obtained as to its exothermic onset temperature (T0, heat of decomposition (ΔHd, isothermal time to maximum rate (TMRiso, and other safety parameters exclusively for loss prevention of runaway reactions and thermal explosions. As a novel finding, LPO mixed with HNO3 can produce the detonation product of 1-nitrododecane. We used differential scanning calorimetry (DSC, thermal activity monitor III (TAM III, and gas chromatography/mass spectrometer (GC/MS analyses of the reactivity for LPO and itself mixed with HNO3 to corroborate the decomposition reactions and reaction mechanisms in these investigations.

  5. Thermal hazard evaluation of lauroyl peroxide mixed with nitric acid.

    Science.gov (United States)

    Tsai, Lung-Chang; You, Mei-Li; Ding, Mei-Fang; Shu, Chi-Min

    2012-01-01

    Many thermal runaway incidents have been caused by organic peroxides due to the peroxy group, -O-O-, which is essentially unstable and active. Lauroyl peroxide (LPO) is also sensitive to thermal sources and is incompatible with many materials, such as acids, bases, metals, and ions. From the thermal decomposition reaction of various concentrations of nitric acid (HNO3) (from lower to higher concentrations) with LPO, experimental data were obtained as to its exothermic onset temperature (T0), heat of decomposition (ΔHd), isothermal time to maximum rate (TMRiso), and other safety parameters exclusively for loss prevention of runaway reactions and thermal explosions. As a novel finding, LPO mixed with HNO3 can produce the detonation product of 1-nitrododecane. We used differential scanning calorimetry (DSC), thermal activity monitor III (TAM III), and gas chromatography/mass spectrometer (GC/MS) analyses of the reactivity for LPO and itself mixed with HNO3 to corroborate the decomposition reactions and reaction mechanisms in these investigations. PMID:22763742

  6. Bile acids increase intracellular Ca2+ concentration and nitric oxide production in vascular endothelial cells

    OpenAIRE

    Nakajima, Toshiaki; Okuda, Yukichi; Chisaki, Keigo; Shin, Wee-Soo; Iwasawa, Kuniaki; Morita, Toshihiro; Matsumoto, Akihiro; Suzuki, Jun-ichi; Suzuki, Seizi; Yamada, Nobuhiro; Toyo-Oka, Teruhiko; Nagai, Ryozo; Omata, Masao

    2000-01-01

    The effects of bile acids on intracellular Ca2+ concentration [Ca2+]i and nitric oxide production were investigated in vascular endothelial cells.Whole-cell patch clamp techniques and fluorescence measurements of [Ca2+]i were applied in vascular endothelial cells obtained from human umbilical and calf aortic endothelial cells. Nitric oxide released was determined by measuring the concentration of NO2−.Deoxycholic acid, chenodeoxycholic acid and the taurine conjugates increased [Ca2+]i concent...

  7. Nitric Acid-Treated Carbon Fibers with Enhanced Hydrophilicity for Candida tropicalis Immobilization in Xylitol Fermentation

    OpenAIRE

    Le Wang; Na Liu; Zheng Guo; Dapeng Wu; Weiwei Chen; Zheng Chang; Qipeng Yuan; Ming Hui; Jinshui Wang

    2016-01-01

    Nitric acid (HNO3)-treated carbon fiber (CF) rich in hydrophilic groups was applied as a cell-immobilized carrier for xylitol fermentation. Using scanning electron microscopy, we characterized the morphology of the HNO3-treated CF. Additionally, we evaluated the immobilized efficiency (IE) of Candida tropicalis and xylitol fermentation yield by investigating the surface properties of nitric acid treated CF, specifically, the acidic group content, zero charge point, degree of moisture and cont...

  8. Studies on photolysis of nitrosyl ruthenium complexes in nitric acid media

    International Nuclear Information System (INIS)

    The photolysis of nitrosyl ruthenium complexes in nitric acid media has been investigated in detail using low pressure mercury lamp (254 nm). The UV spectra of nitrosyl ruthenium complexes is also studied. The experimental results show that the photolysis of nitrosyl ruthenium in nitric acid media obeys pseudo-first order kinetics. The rate constant is affected by the concentration of nitric acid and has a maximum at 2 mol/L HNO3. In temperature range from 10 degree C to 40 degree C, the rate constant decreases with the increasing of the temperature

  9. Study of the sorption of nitric acid by carbons with a varying graphitization rate

    International Nuclear Information System (INIS)

    After having recalled some aspects of the crystalline structure of graphite, and the classification and main properties of lamellar complexes, the author of this research thesis outlines that the graphite-nitric acid complex belongs to the category of spontaneous lamellar complexes which are notably unsteady, or remain steady in presence of an excess of reactant. Then, this research thesis reports the study of the reaction of nitric acid on graphite as well as on pre-graphitic and partially graphitized carbons. The objective is to relate the carbon structure status to its reactivity with respect to nitric acid, and to study the evolution of this reactivity as graphitization progresses

  10. A study on the dissolution of uranium compounds(UO2, AUC) in nitric acid solutions

    International Nuclear Information System (INIS)

    The dissolution behavior of UO2 and AUC powder in nitric acid solutions was investigated to evaluate the performance of chemical decontamination process applicable to and internal surface of metallic system components such as tanks and piping in the uranium conversion plant. It was revealed that the dissolution of UO2 in nitric acid solutions containing low concentration of H2O2 was more effective than that in nitric acid solution without H2O2 as one of the conventional inorganic acid decontamination processes. AUC powder dissolved easily and continuously in nitric acid solutions before the solution pH attains about 3, but above that solution pH uranium concentration in the solution was lowered drastically by recrystallization. It was convinced that pH range of 2.5 ∼ 3 is desired in the decontamination of surface contaminated with AUC

  11. Model nitride irradiated nuclear fuel: production, reaction with water and dilution in nitric acid

    International Nuclear Information System (INIS)

    Samples of the model nuclear fuel (MNF) were made from separately synthesized nitride powders uranium-plutonium, zirconium, lanthanum and metal additives of simulators (Mo, Pd, Rh, Ag) fission products. Synthesis of initial nitride components was carried out from individual oxides, using a carbo-thermal restoration method. From MNF samples baked at a temperature of 1750 C. degrees, were made ceramographic specimens which were investigated by a scanning electron microscope. The analysis showed that distribution of the MNF components and structure of the samples corresponds to distribution of these components in the irradiated nitride fuel. The samples of MNF of nitride fuel were used for carrying out researches on dissolution in water and nitric acid. Experiments on studying the interaction of MNF with water have been made at 20, 50 and 80 C. degrees. The speed of leaching has been determined by a way of measuring the activity of water (Bq/l) in time. It is shown that an increase of temperature leads to an increase of the speed of leaching of plutonium. The formation of a precipitation, allegedly polymeric forms of plutonium, has been observed. The estimated speed of leaching of plutonium from MNF in water at 80 C. degrees is -0,0064 μgPu/(mm2*h). From elements of FP simulators, molybdenum appears to be the most significantly leached. The dissolution of MNF in nitric acid (7,8 and 9,4 mol/l) has been carried out at boiling temperature (106-109 C. degrees). During the process of dissolution, gases were emitted. The assessment of composition of the emitted gases has been carried out. During the filtering of the solutions a precipitate whose weight makes about 2% from the weight of initial fuel has been found. Precipitate represents small powder of metal with gray color. Precipitate was investigated by a scanning electron microscope. The analysis of ranges of absorption of solution showed that the Pu(VI) share to the general content of plutonium in solution can reach

  12. Isothermal heat measurements of TBP-nitric acid solutions

    International Nuclear Information System (INIS)

    Net heats of reaction were measured in an isothermal calorimeter for TBP/HNO3 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-1 at 110 degrees C for an open open-quotes ventedclose quotes system as compared to >1E-3min-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 HNO3. Oxidation in the organic phase was found to be first order in nitric acid and pseudo-zero order in butylnitrate and water

  13. HIRDLS/Aura Level 3 Nitric Acid (HNO3) Zonal Fourier Coefficients V007

    Data.gov (United States)

    National Aeronautics and Space Administration — The "HIRDLS/Aura Level 3 Nitric Acid (HNO3) Zonal Fourier Coefficients" version 7 data product (H3ZFCHNO3) contains the entire mission (~3 years) of HIRDLS data...

  14. Research on the Stability of Diethyl Hydroxylamine in Nitric Acid Medium

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    By the means of the comparison of the extraction of PU(Ⅲ,Ⅳ) and plutonium in the aqueous Phasecontaining salting-free agent, the stability of diethyl hydroxylamine in nitric acid medium is investigated.

  15. Time-resolved laser-induced fluorescence of UO22+ in nitric acid solutions

    International Nuclear Information System (INIS)

    A comparison between nitrogen and tripled Nd-YAG laser source for Time-Resolved Laser-Induced Fluorescence (TRLIF) of uranium in nitric acid solutions in the framework of on-line feasibility has been performed. Hence, for uranium on-line monitoring with fiber optics, nitrogen laser (337 nm), most usual source in TRLIF has several drawback; poor beam quality and non negligible nitric acid absorption at 337 nm. Tripled Nd-YAG laser (355 nm) despite lower uranium absorption coefficient has several advantages: no influence of nitric acid absorption, better beam quality, better fiber transmission and solid state technology. No significant difference for fluorescence spectra and lifetimes are observed for both lasers. Limit of detection for direct determination of uranium in nitric acid by TRLIF is in the μg/l (10-8 M) range for both lasers. (author)

  16. Critical evaluation of pressurized microwave-assisted digestion efficiency using nitric acid oxidizing systems (M7)

    International Nuclear Information System (INIS)

    Full text: The possibilities of enhancement of a medium-pressure microwave-assisted digestion system for sample preparation in trace element analysis of biological material was investigated. Based on optimal digestion conditions for oxidizing systems with nitric acid, different digestion procedures were examined to minimize residual carbon. The substitution of nitric acid and the addition of hydrogen peroxide and ozone to nitric acid was evaluated. The residual carbon content of the digestate was determined coulometrically. Addition of hydrogen peroxide during organic oxidation reactions does not lower the resolved carbon in the solution. Ozone was tested as an additional, potentially non-contaminating, digestion/oxidation system to the nitric acid used in the sample preparation method. (author)

  17. Separation of 230Th (ionium) from uranium ores sulfuric acid and in nitric acid solutions

    International Nuclear Information System (INIS)

    230Th (ionium) is of interest for production of 231Pa, the Pa isotope with the longest half life, and for production of 232U which can be used in radionuclide batteries. Two procedures are presented which have been worked out for separation of 230Th from sulfuric acid and from nitric acid solutions. In the first case the effluents from the anion exchange resins are the starting material for recorvery of 230Th, in the second case the cation exchange resins which are for purification of U. The procedures selected are simple, economic and can be performed in any uranium mill or uranium purification plant without additional investments. (orig.)

  18. Study of Changes in a Palm-Shell-Based Activated Carbon Characteristics by Nitric Acid

    OpenAIRE

    W.M.A.W. Daud; A.H. Houshmand

    2010-01-01

    A palm-shell-based activated carbon (PSAC) was oxidized with nitric acid solutions at different conditions. A 2-level full factorial design was considered for experimental conditions. Adsorption of nitrogen at 77 K, and Temperature-Programmed Desorption (TPD) were used to study the oxidized PSAC. Although, oxidation by nitric acid decreases the surface area and pore volume of PSAC, however it creates a considerable amount of different oxygen groups on the surface of PSAC.

  19. Chemistry of ruthenium in nitric acid solution with special regard to nuclear fuel solutions

    International Nuclear Information System (INIS)

    A review is given concerning the published knowledge about the chemistry of ruthenium in nitric acid solution with special reference to nitric acid nuclear fuel solutions. Possibilities of the spectroscopic description of the different existing ruthenium complexes are discussed and papers are presented dealing with the estimation of the proportions of the different ruthenium compounds in nuclear fuel solutions. Finally, arguments are derived for the preparation of ruthenium-containing model solutions, which adequately simulate the composition of real nuclear fuel solutions. (author)

  20. A bibliographical review on the radiolysis of uranyl nitrate solutions in nitric acid medium

    International Nuclear Information System (INIS)

    A bibliographical study on the effects of ionizing radiation on uranyl nitrate solutions in nitric acid medium was performed, and the state of knowledge on this subject is presented. The main experimental and theoretical results on water, nitric acid and uranium solutions radiolysis are reviewed and critically evaluated. This paper provides a collection of references as an aid to the development of practical applications, and to stimulate new research on fundamental processes in these systems. (author)

  1. Actinoid sorption from nitric acid onto stainless steel. 1. Plutonium sorption and deposition

    International Nuclear Information System (INIS)

    Data are given on the sorption of plutonium from nitric acid onto 12Kh18N10T stainless steel. This is determined by the contact time, the temperature, the plutonium and nitric acid concentrations, and the element state. The uptake varies in the following sequence: Puh>> Pu(IV) > Pu(VI) > Pu(III). The plutonium deposition on reference specimens has been determined with periodic drying

  2. Solubility of uranyl nitrate in nitric acid solutions of aluminum nitrate

    International Nuclear Information System (INIS)

    The solubility of uranyl nitrate in nitric acid solutions of aluminum nitrate at 250C containing 10, 20 and 30 mass % of nitric acid has been studied by the isothermal method. The Schreinemakers method has been used to establish the composition of the solid phases, which has been confirmed by crystallographic and thermographic studies. Data are presented on the viscosity and density of saturated solutions

  3. Thermodynamics of uranium and nitric acid extraction from aqueous solution of TBP/diluent

    International Nuclear Information System (INIS)

    A thermodynamically consistent procedure for predicting distribution equilibria for uranyl nitrate and nitric acid between an aqueous solution and 30 vol % tributyl phosphate (TBP) in a hydrocarbon diluent is studied. Experimental work is developed in order to obtain equilibrium data for the system uranyl nitrate, nitric acid, water and 30 vol % TBP in n-dodecane, at 250C and 400C. The theoretical equilibrium data, obtained with the aid of a computer, are compared with the experimental results. (Author)

  4. The Corrosion Behavior of Ni3(Si,Nb) Alloys in Boiling 70 wt.% Sulfuric Acid

    Science.gov (United States)

    Hsu, Jen-Hsien; Larson, Christopher M.; Newkirk, Joseph W.; Brow, Richard K.; Zhang, San-Hong

    2016-02-01

    Corrosion-resistant Ni3(Si,Nb) alloys are promising materials of construction for hydrogen-production systems based on the sulfur-iodine thermochemical cycle. In this work, the corrosion rates of three different Ni3(Si,Nb) alloys were measured in boiling 70 wt.% sulfuric acid and a three-stage corrosion mechanism was identified, based on the composition and morphology of surface scale that developed. The α(Ni) + β(Ni3Si) eutectic constituent of the alloy microstructure was selectively attacked by acid and, when present, is detrimental to corrosion resistance. The G-phase (Ni16Si17Nb6) is more passive than the β-matrix and seems to contribute to a lower steady-state corrosion rate.

  5. Sorption of Pu(IV) on Aliquat-336 impregnated silica-gel from nitric acid - oxalic acid medium

    International Nuclear Information System (INIS)

    A new ion exchange material prepared by impregnating Aliquat-336 on silica-gel has been investigated for the recovery of plutonium from nitric-oxalic acid solutions. The distribution ratio of Pu(IV) was studied at various concentrations of nitric and oxalic acids. The presence of Al(III) and Fe(III) in the solution, enhances the uptake of Pu(IV). Pu(IV) breakthrough capacities (btc) have been determined using 2.5 ml bed of the ion exchange material column in the absence and the presence of Al(III) and Fe(III) nitrate. The elution behavior of Pu(IV) was also studied using nitric acid solutions containing reducing agents. More than 90% of plutonium could be recovered from nitric-oxalic acid solutions. (author)

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

    International Nuclear Information System (INIS)

    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 approximately2.5 g of sludge (dry basis). The high solids loading test was conducted with approximately7 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

  7. Contribution to the study of the oxidation reaction of Np(V) by nitric acid catalyzed par nitrous acid

    International Nuclear Information System (INIS)

    The oxidation reaction kinetics of Np(V) to Np(VI) by nitric acid catalyzed by nitrous acid was studied. In a first part, a detailed bibliographical survey was made of the oxidation-reduction reactions of U, Np, Pu, Am with nitrous and nitric acids (51 references). It is shown that only when both the organic and aqueous phases are mixed up, the extraction of a reaction product (NpVI) induces an equilibrium displacement. TBP was used as solvent. It is shown that the extraction of nitrous acid from the solvent enables the nitrous acid concentration to be kept constant and in the same order of magnitude than that of Np. This enables to show that Np(V) and nitrous acid have no simple orders. The temperature and nitric acid concentration dependence was studied. It is shown that tetravalent nitrogen must play a major part in the Np(V) oxidation

  8. Corrosion of type 304L stainless steel in boiling dilute neptunium nitrate solution

    International Nuclear Information System (INIS)

    Corrosion of type 304L stainless steel in nitric acid solution containing neptunium was studied under immersion and heat-transfer condition. Corrosion rates of stainless steel were obtained by the weight loss measurement and the quantitative analysis of metallic ions dissolved in solution. The surface morphology was observed by scanning electron microscopy. The corrosion acceleration mechanism was investigated by polarization measurement and spectrophotometry. The corrosion rate in boiling 9M nitric acid was accelerated by addition of neptunium. The corrosion of stainless steel was promoted under heat-transfer condition compared to immersion condition. In polarization measurements, the cathodic current was increased by addition of neptunium. Spectrophotometric measurements showed the oxidization of neptunium in boiling nitric acid. It was suggested that the accelerated corrosion in nitric acid solution containing neptunium was caused by re-oxidation of neptunium. (author)

  9. The Chemistry Study Of Uranium And Transition Elements In Mixture Of Nitric Acid And Sulfuric Acid Were Done

    International Nuclear Information System (INIS)

    The uranium and transition elements were contained in the waste of technetium-99 generator productions to be formed by irradiated uranium. This waste medium is low concentration of nitric acid and sulfuric acid. The tendency of uranium in this medium to form uranyl sulfate complex, the compound of uranyl sulfate belong to heteropoly compounds and is an acid. The transition elements in mixture of nitric acid and sulfuric acid solutions have tendency to form cation complex compound According to difference of the chemical properties of uranium and transition elements, the base reagent can be used for recovery of uranium from this solution

  10. Progress report on nitric-phosphoric acid oxidation

    International Nuclear Information System (INIS)

    The purpose of this program has been to demonstrate a nitric-phosphoric acid destruction technology which can treat a heterogeneous waste stream. This technology is being developed to convert hazardous liquid and solid organics to inorganic gases and salts while simultaneously performing a surface decontamination of the noncombustible items. Pu-238 waste is an issue because it must be shipped to WIPP. However, the presence of organics and Pu-238 waste is an issue because it must be shipped to WIPP. However, the presence of organics and Pu-238 exceeds packaging requirements because of concerns of hydrogen generation. If the TRU can be separated from the organics, the allowable heat load of a container increases a factor of 25. More importantly, since the current shipping package is limited by volume and not heat loading, destroying the organic compounds and decontaminating noncombustible can potentially create a three-order magnitude decrease in the number of shipments that must be made to WIPP. The process envisioned will be configured to handle 1 million pounds (as of 12/91) of a wide range of solid TRU-contaminated waste of which 600,000 pounds is combustible. The process will oxidize the combustibles (a mixture of 14% cellulose, 3% rubber, 64% plastics, 9% absorbed oil, 4% resins and sludges, and 6% miscellaneous organics) without requiring separation from the 400,000 pounds of noncombustibles. The system is being developed to operate below 200 C at moderate pressures (0--15 psig). This report primarily discusses results obtained over the past 3 1/2 months and their impact on the feasibility of a pilot-scale system

  11. Isothermal heat measurements of TBP-nitric acid solutions

    International Nuclear Information System (INIS)

    Net heats of reaction were measured in an isothermal calorimeter for both single phase (organic) and two phase (organic and aqueous) TBP/HNO3 reacting solutions at temperatures above 100 C. The oxidation rate constant was determined to be 5.4E-4 min-1 at 110 C for an open ''vented'' system as compared to 1.33 E-3 min-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-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 HNO3 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 HNO3 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

  12. Evaporation and NARS Nitric Acid Mass Balance Summary: 2000--2005

    International Nuclear Information System (INIS)

    A compilation of the historical nitric acid processing data for the evaporation and nitric acid recycle system (NARS) in TA-55 has provided general acid mass balance trends, as well as the location of missing information in both the evaporation system and NARS data logs. The data were accumulated during the calendar years 2000 to 2005. After making a number of processing assumptions, the empirical system information was used to create an interactive spreadsheet that predicts, with moderate accuracy, some of the various stream variables for the combined evaporation and acid recycle processes. Empirical data and interactive calculations were compared to an Aspen Plus(trademark) simulation of the process

  13. GADOLINIUM OXALATE SOLUBILITY MEASUREMENTS IN NITRIC ACID SOLUTIONS

    Energy Technology Data Exchange (ETDEWEB)

    Pierce, R.

    2012-02-22

    HB-Line will begin processing Pu solutions during FY2012 that will involve the recovery of Pu using oxalate precipitation and filtration. After the precipitation and filtration processes, the filtrate solution will be transferred from HB-Line to H-Canyon. The presence of excess oxalate and unfiltered Pu oxalate solids in these solutions create a criticality safety issue if they are sent to H-Canyon without controls in H-Canyon. One approach involves H-Canyon receiving the filtrate solution into a tank that is poisoned with soluble gadolinium (Gd). Decomposition of the oxalate will occur within a subsequent H-Canyon vessel. The receipt of excess oxalate into the H-Canyon receipt tanks has the potential to precipitate a portion of the Gd poison in the receipt tanks. Because the amount of Gd in solution determines the maximum amount of Pu solids that H-Canyon can receive, H-Canyon Engineering requested that SRNL determine the solubility of Gd in aqueous solutions of 4-10 M nitric acid (HNO{sub 3}), 4-12 g/L Gd, and 0.15-0.25 M oxalic acid (H{sub 2}C{sub 2}O{sub 4}) at 25 C. The target soluble Gd concentration is 6 g/L. The data indicate that the target can be achieved above 6 M HNO{sub 3} and below 0.25 M H{sub 2}C{sub 2}O{sub 4}. For 6 M HNO{sub 3}, 10.5 g/L and 7 g/L Gd are soluble in 0.15 M and 0.25 M H{sub 2}C{sub 2}O{sub 4}, respectively. In 4 M HNO{sub 3}, the Gd solubility drops significantly to 2 g/L and 0.25 g/L in 0.15 M and 0.25 M H{sub 2}C{sub 2}O{sub 4}, respectively. The solubility of Gd at 8-10 M HNO{sub 3} exceeds the solubility at 6 M HNO{sub 3}. The data for 4 M HNO{sub 3} showed good agreement with data in the literature. To achieve a target of 6 g/L soluble Gd in solution in the presence of 0.15-0.25 M oxalate, the HNO{sub 3} concentration must be maintained at or above 6 M HNO{sub 3}.

  14. The resistance of ion exchangers to nitric acid and radiation. Pt. 3

    International Nuclear Information System (INIS)

    The stability to gamma radiation in the dose range from 0.1 to 2 MGy of the Wof MC 50 Chelon exchanger with functional groups of the aminoacetic acid and iminodiacetic acid type has been studied in the air-dry state as well as in the presence of nitric acid. To characterize the radiation-induced reaction it was necessary to determine the capacity of the COOH groups, the nitrogen content, and the amount and composition of radiolysis gas and record the infrared and mass spectra of the irradiated samples. In the case of irradiation in the air-dry state, in water, and in 1 n nitric acid, the main reaction is decarboxylation with G values of 13 +- 2, whereas irradiation in nitric acid in a range of concentration greater than or equal to 7 mol/l results in rapid oxidative breakdown of the functional groups of the resin being superimposed on the radiation-induced reaction. (orig.)

  15. Corrosion properties of high silicon iron-based alloys in nitric acid

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The effect of copper and rare-earth elements on corrosion behavior of ~iigh silicon iron-based alloys in nitric acid was studied by means of static and loading current corrosion experiments. The anodic polarization curve was also made to discuss the corrosion mechanism. The examination on alloy microstructure and SEM corrosion pattern showed that when silicon content reached 14.5%, the Fe3Si phase appeared and the primary structure of the iron-base alloy was ferrite. When adding 4.57% copper in the iron alloy, its corrosion resistance in static diluted sulfuric acid was improved while its corrosion resistance and electrochemical corrosion properties in the nitric acid were decreased. In contrast, the addition of rare earth elements could improve the corrosion properties in all above conditions including in static diluted sulfuric acid and in nitric acid.

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

    International Nuclear Information System (INIS)

    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

  17. Kinetics of reaction between acetic acid and Ag2+ in nitric acid medium

    International Nuclear Information System (INIS)

    The reaction kinetics between acetic acid and Ag2+ in nitric acid medium is studied by spectrophotometry. The effects of concentrations of acetic acid (HAc), H+, NO3- and temperature on the reaction are investigated. The rate equation has been determined to be -dc(Ag2+)/dt=kc(Ag2+)c(HAc)c-1(H+), where k = (610±15) (mol/L)-1·min-1 with an activation energy of about (48.8±3.5) kJ·mol-1 when the temperature is 25degC and the ionic strength is 4.0 mol/L. The reduction rate of Ag2+ increases with the increase of HAc concentration or temperature and the decrease of HNO3 concentration. However, the effect of NO3- concentrations on the reaction rate is negligible. (author)

  18. Nitric oxide secretion in human conjunctival fibroblasts is inhibited by alpha linolenic acid

    OpenAIRE

    Erdinest, Nir; Shohat, Noam; Moallem, Eli; Yahalom, Claudia; Mechoulam, Hadas; Anteby, Irene; Ovadia, Haim; Solomon, Abraham

    2015-01-01

    Purpose It is known that both human conjunctival fibroblasts (HCF) and corneal epithelial (HCE) cells contribute to the inflammatory process in the ocular surface by releasing inflammatory cytokines. In addition, nitric oxide (NO) has an important role in inflammatory responses in the ocular surface. In the present study, we aimed to characterize the capacity of these cells to release nitric oxide in response to cytokines and Lipopolysaccharide (LPS), and show that Alpha-linoleic acid (ALA) i...

  19. Thermodynamics and kinetics of thermal decomposition of dibutylalkyl and dipentylalkyl phosphonate-nitric acid systems

    International Nuclear Information System (INIS)

    Highlights: • Thermal stability of neat and nitric acid solvated DBalP and DPalP have been studied for the first time. • Incompressible gases and reddish viscous or black solid residues were formed on decomposition. • Decomposition of acid solvated phosphonates was found to be exothermic and follows first order kinetics. • The thermodynamic and kinetic parameters were derived wherever possible. - Abstract: Thermal stability of neat and nitric acid-solvated dibutylalkyl and dipentylalkyl phosphonates was studied under closed air ambience using an adiabatic calorimeter. Enthalpies and kinetic parameters for the decomposition reaction were derived wherever possible and are reported for the first time. The neat compounds were found to be stable up to 555 K while the nitric acid-solvated phosphonates decomposed at lower temperatures (370–403 K) with exothermic rise in temperature and pressure invariably producing incompressible gases. Decomposition of all these acid-solvates followed first order kinetics. The rise in temperature and pressure was found to be strongly dependent on nitric acid content of the acid-solvate. While the neat phosphonates produced solid black residue, the acid-solvates produced a viscous reddish-brown residue on decomposition. Heat capacities (Cp), of acid-solvates (DBPrP·0.6HNO3, DBBP·0.6HNO3 and DBPP·0.6HNO3) were measured at constant pressure using a heat flux type differential scanning calorimeter in the temperature range 305–350 K

  20. Zirconium distribution between two phases: di-2-ethyl-hexyl phosphoric acid diluted in dodecane and aqueous phase of nitric acid

    International Nuclear Information System (INIS)

    Zirconium extraction by di-2-ethyl-hexyl phosphoric acid, from 0.5 to 10M nitric acid solutions is measured. The mechanism is independent of the acidity of the aqueous phase; a carbonic complex of zirconium nitrate is extracted. From a concentration 6M HNO3, an important extraction of nitric acid is noted. Consequences are brought out

  1. Mechanism of the extraction of nitric acid and water by organic solutions of tertiary alkyl-amines

    International Nuclear Information System (INIS)

    The micellar aggregation of tri-alkyl-ammonium nitrates in low polarity organic solvents has been verified by viscosity, conductivity and sedimentation velocity measurements. The aggregation depends upon the polarity of solvent, the length of the alkyl radicals and the organic concentration of the various constituents (tri-alkyl-ammonium nitrate, tri-alkyl-amine, nitric acid, water). The amine salification law has been established and the excess nitric acid and water solubilities in the organic solutions have been measured. Nitric acid and water are slightly more soluble in micellar organic solutions than in molecular organic solutions. A description of excess nitric acid containing tri-alkyl-ammonium nitrate solutions is proposed. (author)

  2. Characteristics and mechanism of explosive reactions of Purex solvents with Nitric Acid at elevated temperatures

    International Nuclear Information System (INIS)

    This investigation was undertaken to make clear the energetic properties and mechanism of explosive decomposition of Purex solvent systems (TBP/n-Dodecane/HNO3) by Nitric Acid at elevated temperatures using a calorimetric technique (DSC, ARC) and a chromatographic technique (GC, GC/MS). The measurement of exothermic events of solvent-HNO3 reactions using DSC with a stainless steel sealed cell showed distinct two peaks with maxima at around 170 and 320degC, respectively. The peak at around 170degC was mainly attributed to the reactions of dealkylation products (n-butyl nitrate) of TBP and the solvent with nitric acid, and the peak at around 320degC was attributed to the exothermic decomposition of nitrated dodecanes formed in the foregoing exothermic reaction of dodecane with nitric acid. By using the data obtained in ARC experiments, activation energies of 123.2 and 152.5 kJ/mol were determined for the exothermic reaction of TBP with nitric acid and for the exothermic pyrolysis of n-butyl nitrate, respectively. Some possible pathways were considered for the explosive decomposition of TBP by nitric acid at elevated temperatures. (author)

  3. Effects of Nitric Acid Concentration on the Stability of Alumina Sols

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Alumina sols with a mlar ratio of 1: 50 between aluminum sec- butoxide ( ASB ) and H2 O werefabricated by adding various amounts of nitric acid.The particle shape, zeta potential, polydispersity and effective particle size of alumina sol were examined by a TEM, a zeta PALS granularity analyzer and a zetaPALS zeta potential analyzer, respectively.By analyzing the change of zeta potential and double- layer thickness with nitric acid concentration, the potential energy curves of colloidal particles were mapped on the basis of DLVO theory, and the effects of nitric acid concentration on the stability of alumina sols were intensively studied.The results show that for the alumina sols with a mol ratio of 1: 50 between ASB and H2 O, the total interaction energy of the colloidal particle is at a maximum when the nitric acid concentration is 0.22 mol/ L.Therefore, the stability of the colloid reaches optimum at the nitric acid concentration of 0.22 mol/L.

  4. GADOLINIUM OXALATE SOLUBILITY MEASUREMENTS IN NITRIC ACID SOLUTIONS

    Energy Technology Data Exchange (ETDEWEB)

    Pierce, R. A.

    2012-03-12

    HB-Line will begin processing Pu solutions during FY2012 that will involve the recovery of Pu using oxalate precipitation and filtration. After the precipitation and filtration processes, the filtrate solution will be transferred from HB-Line to H-Canyon. The presence of excess oxalate and unfiltered Pu oxalate solids in these solutions create a criticality safety issue if they are sent to H-Canyon without controls in H-Canyon. One approach involves H-Canyon receiving the filtrate solution into a tank that is poisoned with soluble gadolinium (Gd). Decomposition of the oxalate will occur within a subsequent H-Canyon vessel. The receipt of excess oxalate into the H-Canyon receipt tanks has the potential to precipitate a portion of the Gd poison in the receipt tanks. Because the amount of Gd in solution determines the maximum amount of Pu solids that H-Canyon can receive, H-Canyon Engineering requested that SRNL determine the solubility of Gd in aqueous solutions of 4-10 M nitric acid (HNO{sub 3}), 4-12 g/L Gd, and 0.15-0.25 M oxalic acid (H{sub 2}C{sub 2}O{sub 4}) at 25 °C. The target soluble Gd concentration is 6 g/L. The data indicate that the target can be achieved above 6 M HNO{sub 3} and below 0.25 M H{sub 2}C{sub 2}O{sub 4}. At 25 °C, for 6 M HNO{sub 3}, 11 g/L and 7 g/L Gd are soluble in 0.15 M and 0.25 M H{sub 2}C{sub 2}O{sub 4}, respectively. In 4 M HNO{sub 3}, the Gd solubility drops significantly to 2.5 g/L and 0.8 g/L in 0.15 M and 0.25 M H{sub 2}C{sub 2}O{sub 4}, respectively. The solubility of Gd at 8-10 M HNO{sub 3} exceeds the solubility at 6 M HNO{sub 3}. The data for 4 M HNO{sub 3} showed good agreement with data in the literature. To achieve a target of 6 g/L soluble Gd in solution in the presence of 0.15-0.25 M oxalate, the HNO{sub 3} concentration must be maintained at or above 6 M HNO{sub 3}. The solubility of Gd in 4 M HNO{sub 3} with 0.15 M oxalate at 10 °C is about 1.5 g/L. For 6 M HNO{sub 3} with 0.15 M oxalate, the solubility of Gd at 10

  5. Investigation into nitric acid extraction by di-2-ethylhexylphosphoric acid and its acid zirconium (4) and hafnium (4) salts

    International Nuclear Information System (INIS)

    Using IR spectroscopy methods mechanism of nitric acid extraction by solutions of di-2-ethylhexylphosphoric acid HX and its zirconium (4) and hafnium (4) polymeric salts in decane is investigated. Di-2-ethylhexylphosphoric acid extracts HNO3 by usual coordination mechanism adding HNO3 molecules to P=O group of (XH)2 dimer by means of its proton. Zr4 and Hf4 acid salts add HNO3 molecules bidentately due to availability in polymeric molecules of extractant metal atoms - electron acceptors. Structure of separate fragments, being part of polymeric products of adding HNO3 to acid salts and containing nonequivalent POO-groups, is determined. IR spectra absorption band interpretation is carried out

  6. Observation of gaseous nitric acid production at a high-energy proton accelerator facility

    CERN Document Server

    Kanda, Y; Nakajima, H

    2005-01-01

    High-energy protons and neutrons produce a variety of radionuclides as well as noxious and oxidative gases, such as ozone and nitric acid, in the air mainly through the nuclear spallation of atmospheric elements. Samples were collected from the surfaces of magnets, walls, and floors in the neutrino beamline tunnel and the target station of the KEK 12-GeV proton synchrotron facility by wiping surfaces with filter paper. Considerably good correlations were found between the amounts of nitrate and tritium and between those of nitrate and /sup 7/Be. This finding gives evidence that at high-energy proton facilities, nitric acid is produced in the radiolysis of air in beam- loss regions. Also, the nitric acid on the surfaces was found to be desorbed and tended to be more uniform throughout the tunnel due to air circulation. The magnitude of diminishing from the surfaces was in the order of tritium>nitrate>/sup 7/Be1).

  7. Separation of strontium nitrate from nitric-acid extract during production of compound fertilizers

    International Nuclear Information System (INIS)

    The process is studied of isolation of a strontium-containing concentrate formed on decomposition of apatite by nitric acid with previous concentration of the nitric-acid extract by centrifuging or precipitation. The effect of the HNO3 concentration on the degree of isolation of strontium nitrate has been studied. It is shown that the strontium nitrate fraction in the nitric-acid extract in the solid phase is proportional to the HNO3 concentration. When using precipitation, the highest yield of Sr(NO3)2 to the concentrated product was obtained with the use of 54%HNO3. With the centrifuging method, the yield of the strontium nitrate to the concentrated product increases from 54 to 78% with respect to the apatite as the HNO3 concentration increases from 50 to 58%

  8. Observation of gaseous nitric acid production at a high-energy proton accelerator facility

    International Nuclear Information System (INIS)

    High-energy protons and neutrons produce a variety of radionuclides as well as noxious and oxidative gases, such as ozone and nitric acid, in the air mainly through the nuclear spallation of atmospheric elements. Samples were collected from the surfaces of magnets, walls, and floors in the neutrino beamline tunnel and the target station of the KEK 12-GeV proton synchrotron facility by wiping surfaces with filter paper. Considerably good correlations were found between the amounts of nitrate and tritium and between those of nitrate and 7Be. This finding gives evidence that at high-energy proton facilities, nitric acid is produced in the radiolysis of air in beam-loss regions. Also, the nitric acid on the surfaces was found to be desorbed and tended to be more uniform throughout the tunnel due to air circulation. The magnitude of diminishing from the surfaces was in the order of tritium>nitrate>7Be

  9. TESTING OF 304L STAINLESS STEEL IN NITRIC ACID ENVIRONMENTS WITH FLUORIDES AND CHLORIDES

    Energy Technology Data Exchange (ETDEWEB)

    Mickalonis, J.

    2010-10-04

    Impure radioactive material processed in nitric acid solutions resulted in the presence of chlorides in a dissolver fabricated from 304L stainless steel. An experimental program was conducted to study the effects of chloride in nitric acid/fluoride solutions on the corrosion of 304L stainless steel. The test variables included temperature (80, 95, and 110 C) and the concentrations of nitric acid (6, 12, and 14 M), fluoride (0.01, 0.1, and 0.2 M) and chloride (100, 350, 1000, and 2000 ppm). The impact of welding was also investigated. Results showed that the chloride concentration alone was not a dominant variable affecting the corrosion, but rather the interaction of chloride with fluoride significantly affected corrosion.

  10. Method and apparatus for processing ruthenium-containing nitric acid solution by evaporization

    International Nuclear Information System (INIS)

    In evaporization treatment of ruthenium-containing nitric acid in the reprocessing of spent fuels, evaporization of ruthenium is suppressed to improve the decontamination coefficient and corrosion resistance of the constituent materials for the apparatus. In view of the above, ruthenium ions in nitric acid are converted not merely into usual nitrosyl ruthenium complex but into nitrosyl ruthenium complex coordinated with nitro groups before evaporization processing. This can be attained by introducing gaseous nitrogen oxide as small bubbles by way of an introduction tube to a solution of ruthenium-containing nitric acid. Accordingly, when a solution containing nitro complex coordinated with nitro groups is sent into the evaporization tube for evaporation treatment, ruthenium nitrosyl-nitro complex can always be present at a concentration higher than a predetermined level in the evaporization tube to suppress the evaporization of ruthenium. (T.M.)

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

    International Nuclear Information System (INIS)

    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

  12. DISSOLUTION OF PLUTONIUM METAL IN 8-10 M NITRIC ACID

    Energy Technology Data Exchange (ETDEWEB)

    Rudisill, T.; Pierce, R.

    2012-02-21

    The H-Canyon facility will be used to dissolve Pu metal for subsequent purification and conversion to plutonium dioxide (PuO{sub 2}) using Phase II of HB-Line. To support the new mission, the development of a Pu metal dissolution flowsheet which utilizes concentrated (8-10 M) nitric acid (HNO{sub 3}) solutions containing potassium fluoride (KF) is required. Dissolution of Pu metal in concentrated HNO{sub 3} is desired to eliminate the need to adjust the solution acidity prior to purification by anion exchange. The preferred flowsheet would use 8-10 M HNO{sub 3}, 0.015-0.07 M KF, and 0.5-1.0 g/L Gd to dissolve the Pu up to 6.75 g/L. An alternate flowsheet would use 8-10 M HNO{sub 3}, 0.1-0.2 M KF, and 1-2 g/L B to dissolve the Pu. The targeted average Pu metal dissolution rate is 20 mg/min-cm{sup 2}, which is sufficient to dissolve a 'standard' 2250-g Pu metal button in 24 h. Plutonium metal dissolution rate measurements showed that if Gd is used as the nuclear poison, the optimum dissolution conditions occur in 10 M HNO{sub 3}, 0.04-0.05 M KF, and 0.5-1.0 g/L Gd at 112 to 116 C (boiling). These conditions will result in an estimated Pu metal dissolution rate of {approx}11-15 mg/min-cm{sup 2} and will result in dissolution times of 36-48 h for standard buttons. The recommended minimum and maximum KF concentrations are 0.03 M and 0.07 M, respectively. The maximum KF concentration is dictated by a potential room-temperature Pu-Gd-F precipitation issue at low Pu concentrations. The purpose of the experimental work described in this report was two-fold. Initially a series of screening experiments was performed to measure the dissolution rate of Pu metal as functions of the HNO{sub 3}, KF, and Gd or B concentrations. The objective of the screening tests was to propose optimized conditions for subsequent flowsheet demonstration tests. Based on the rate measurements, this study found that optimal dissolution conditions in solutions containing 0.5-1.0 g/L Gd

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

    International Nuclear Information System (INIS)

    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

  14. The dynamics of nitric acid production and the fate of nitrogen oxides

    OpenAIRE

    Russell, Armistead G.; McRae, Gregory J.; Cass, Glen R.

    1985-01-01

    A mathematical model is used to study the fate of nitrogen oxides (NO_x) emissions and the reactions responsible for the formation of nitric acid (HNO_3). Model results indicate that the majority of the NO_x inserted into an air parcel in the Los Angeles basin is removed by dry deposition at the ground during the first 24 h of travel, and that HNO_3 is the largest single contributor to this deposition flux. A significant amount of the nitric acid is produced at night by N_2O_5 hydrolysis. Per...

  15. Modified density equation for aqueous solution with plutonium(IV) and nitric acid

    International Nuclear Information System (INIS)

    In order to calculate criticality parameters for solution systems, the number densities of nuclides are needed and usually calculated by use of density equations. For the system of aqueous solution with Pu(IV) and nitric acid, Maimoni's equation based on Hofstetters' density data was often used, but its reliability was not thoroughly examined. The author, therefore, derived a modified density equation by regression analysis for Hofstetters' data, adding the authors' density data of aqueous solution with nitric acid. Comparison between both equations showed that the modified density equation gives more reliable densities in the wide range of temperature and concentration. (author)

  16. Radiation-thermal decomposition of nitric and acetic acids in the aqueous nitrate solution

    International Nuclear Information System (INIS)

    Kinetics of radiation, thermal and radiation-thermal decompositions of nitric and acetic acid mixture was investigated in aqueous sodium nitrate solution in homogeneous conditions as well as by interaction of solid phase as sand rock. Temperature dependences of rate of radiation, thermal and radiation-thermal decompositions of the acids were calculated using experimental data. Resulting solutions make possible the calculation of acid decomposition dynamics accounting conditions of underground radioactive waste disposals

  17. Thermodynamic and kinetic modelling of the reduction of concentrated nitric acid

    International Nuclear Information System (INIS)

    This research thesis aimed at determining and quantifying the different stages of the reduction mechanism in the case of concentrated nitric acid. After having reported the results of a bibliographical study on the chemical and electrochemical behaviour of concentrated nitric media (generalities, chemical equilibriums, NOx reactivity, electrochemical reduction of nitric acid), the author reports the development and discusses the results of a thermodynamic simulation of a nitric environment at 25 C. This allowed the main species to be identified in the liquid and gaseous phases of nitric acid solutions. The author reports an experimental electrochemical investigation coupled with analytic techniques (infrared and UV-visible spectroscopy) and shows that the reduction process depends on the cathodic overvoltage, and identifies three potential areas. A kinetic modelling of the stationary state and of the impedance is then developed in order to better determine, discuss and quantify the reduction process. The application of this kinetic model to the preliminary results of an electrochemical study performed on 304 L steel is then discussed

  18. Thermodynamics and kinetics of thermal decomposition of dibutylalkyl and dipentylalkyl phosphonate-nitric acid systems

    International Nuclear Information System (INIS)

    Tributyl phosphate (TBP) is used in the reprocessing industry for the separation of uranium and plutonium from the spent nuclear fuels by PUREX process. A variety of dialkylalky/phosphonates were synthesised and their extraction behaviour on actinides was studied in this laboratory. The superior extraction characteristics of phosphonates make them useful for several metal recovery applications in the nuclear fuel cycle. However, higher solubility of phosphonates in aqueous phase as compared to TBP, introduces higher chances of the formation of thermally active 'red oil' like substances during the evaporation of aqueous streams. Thermal stability of neat and nitric acid solvated homologues of four dibutylalkyl phosphonates namely, dibutylpropyl phosphonate (DBPrP), dibutylbutyl phosphonate (DBBP), dibutylpentyl phosphonate (DBPP), dibutylhexyl phosphonate (DBHeP), and two dipentylalkyl phosphonates viz. dipentylbutyl phosphonate (DPBP), dipentylhexyl phosphonate (DPHeP) were studied. Experiments were conducted using an adiabatic calorimeter in heat-wait-search mode. Various stoichiometry of nitric acid-solvated DBalP and DPalP were prepared by equilibrating the respective organic with 4-15.6 M nitric acid followed by separation. Neat DBalP and DPalP are stable up to the temperature of ∼ 555 K while their acid-solvates decomposed in the temperature range 380-403 K. The results also indicated that the presence of nitric acid accelerated the decomposition of phosphonates. Decomposition of these acid solvated phosphonates is found to be exothermic and follows first order kinetics. The onset temperature, adiabatic temperature rise, pressure rise, decomposition enthalpy and activation energy were found to strongly depend on the nitric acid content of the acid-solvates. The studies also indicate that dibutylalkyl and dipentylalkyl phosphonates are also prone to form 'red oil' like substances under extreme conditions and can lead to run-away reactions

  19. Material compatibility evaluation for DWPF nitric-glycolic acid-literature review

    Energy Technology Data Exchange (ETDEWEB)

    Mickalonis, J. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Skidmore, E. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2013-06-01

    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.

  20. The distribution of acid, water, methanol, ethanol and acetone between mixed aqueous-organic nitric acid solutions of trilaurylammoniumnitrate in cyclohexane

    International Nuclear Information System (INIS)

    The distribution of acid, water, methanol, ethanol and acetone between mixed aqueous-organic nitric acid solutions and solutions of trilaurylammoniumnitrate in cyclohexane has been investigated. The distribution of acid rises with increasing concentrations of nitric acid, methanol, ethanol and acetone in the mixed aqueous-organic phase. The effect of the organic additives in increasing the distribution of the acid is methanol< ethanol< acetone. The concentration of nitric acid in the organic phase can be calculated by a formula similar to that describing the extraction from pure aqueous solutions. The distribution curves of water, methanol and ethanol resemble each other, all of them showing a minimum, when the distribution ratio is plotted versus the nitric acid concentration in the mixed aqueous-organic phase. The acetone distribution decreases steadily with increasing nitric acid concentration. The shape of the curves is briefly discussed. (T.G.)

  1. Stability of ion exchangers against treatment with nitric acid and radiation. Pt. 2

    International Nuclear Information System (INIS)

    The change in the sorption properties of chelating ion exchangers with amino acetic acid and amino diacetic acid groups of the type Wof MC 50, Chelex 100 and Dowex A-1 after treatment with nitric acid is examined. The nitric acid concentration is varied in the range 1-10.5 N; the reaction time varied from 0.5 to 25 h. The reaction temperature was 680C. By destruction of the amino diacetic acid groups the sorption properties are changed. The sorption of cations (Cs+ -0.019 N NH4C1) decreases, goes through a minimum and increases again when the COOH capacity is increased. The sorption of anions (TcO-4 -1 N HNO3) and anionic complexes (PdC142- -1 N HC1) decreases in correlation with the N-content. (orig.)

  2. The stability of ion exchangers towards nitric acid and radiation. 1

    International Nuclear Information System (INIS)

    The behaviour of the chelating ion exchangers Wofatit MC 50, Dowex A 1 and Chelex 100 with aminoacetic acid - and iminodiacetic acid-groups towards nitric in the range of the concentration 1 ... 10.5 mol/l and at temperatures 0C was determined. It is found that the COOH capacity and the N content are rapidly reduced leading to the formation of CO2 and N2. If the exposure to HNO3 continues there is again a rise in the COOH capacity. The i.r.- and mass spectra show that the iminodiacetic acid-groups are destroyed by nitrosative cleavage and CHO groups result, which are then oxidized to COOH groups. The mass spectrum shows that the aminoacetic acid-groups of the resin are nitrosated, which has also been confirmed by the use of nitric acid labelled with 15N. (author)

  3. Disposition of PUREX contaminated nitric acid the role of stakeholder involvement

    International Nuclear Information System (INIS)

    What does the United States space shuttle and the Hanford PUREX facility's contaminated nitric acid have in common. Both are reusable. The PUREX Transition Project has achieved success and, minimized project expenses and waste generation by looking at excess chemicals not as waste but as reusable substitutes for commercially available raw materials. This philosophy has helped PUREX personnel to reuse or recycle more than 2.5 million pounds of excess chemicals, a portion of which is the slightly contaminated nitric acid. After extensive public review, the first shipment of contaminated acid was made in May 1995. Removal of the acid was completed on November 6, 1995 when the fiftieth shipment left the Hanford site. This activity, which avoided dispositioning the contaminated acid as a waste, generated significantly more public input and concern than was expected. One of the lessons learned from this process is to not underestimate public perceptions regarding the reuse of contaminated materials

  4. Investigation of the direct and indirect electrochemical oxidation of hydrazine in nitric acid medium on platinum

    International Nuclear Information System (INIS)

    In nuclear fuel processing by the PUREX process, the purification of plutonium in nitric acid medium requires the oxidation of Pu(III) to Pu(IV), and of hydrazinium nitrate to nitrogen. The study helped to characterize the electrochemical behavior of the oxidation of hydrazinium nitrate and the reduction of nitric acid to nitrous acid, a compound which can chemically oxidize hydrazinium nitrate and Pu(III). Electro-analytical studies on polycrystalline platinum showed that hydrazine is oxidized in two potential zones, which depend on the surface texture of the platinum anode. Electrolysis in separate compartments, carried out in medium-acid media (2 and 4 mo/l) in the potential zone where these processes take place, showed that, at 0.9 V/ECS, the hydrazine oxidation reactions involved are: a four-electron process (75 %) with nitrogen formation and a one-electron process (25 %) with formation of nitrogen and ammonium ion. By contrast, electrolysis carried out at 0.65 V/ECS (with reactivation of the electrode at - 0.2 V/ECS to remove the poison from the platinum) allowed the selective oxidation of hydrazine to nitrogen by the four-electron reaction. Nitric acid can only be reduced to nitrous acid in the absence of hydrazine. For medium-acid media (≤ 6 mol/l), this reaction takes place at potentials below - 0.2 V/ECS. However, the production rate of nitrous acid (partial order 0 with respect to nitric acid) is very low compared with the values obtained for strongly-acid media (6 to 10 mol/l) at the potential of - 0.1 V/ECS. Note that, in concentrated nitric medium, the selectivity of the reduction reaction is 47 to 85 % for nitrous acid, depending on the nitric acid concentration (6 to 10 mol/l) and the potential imposed (- 0.1 ≤ E ≤ 0.6 V/ECS). A kinetic study helped to determine the hydrazine oxidation rates as a function of the operating conditions. In all cases, the reaction rate is of partial order 0 with respect to hydrazine. These studies accordingly

  5. Determination of small amounts of nitric acid in the presence of large amounts of uranium (VI) and extraction of nitric acid into TBP solutions highly loaded with uranyl nitrate

    International Nuclear Information System (INIS)

    A new method for the determination of small amounts of nitric acid in the presence of large amounts of uranium(VI) was elaborated. The method is based on the precipitation of uranium(VI) as iodate and subsequent alkalimetric titration of the acid in the supernatant. The extraction of nitric acid and uranium(VI) with 30% TBP in dodecane was studied at high loading of the organic phase with uranyl nitrate and at 25, 40 and 600C. The results are compared with available published data on the extraction of nitric acid under similar conditions. (orig.)

  6. Extraction of nitric acid from aqueous media with OφD(iB)CMPO-n-dodecane

    International Nuclear Information System (INIS)

    A study of the extraction characteristics of nitric acid with octyl(phenyl)-N,N-diisobutylcarbamoylmethyl phosphine oxide [OφD(iB)CMPO or, simply, CMPO] was conducted. In the experimental program, CMPO was dissolved in n-dodecane to produce the organic extracting medium. The objectives of the project were to infer extraction stoichiometry and to estimate equilibrium constants for the extraction of nitric acid with the CMPO extractant. Experiments were performed over a limited range of concentrations to avoid conditions favoring formation of a third phase. Aqueous nitric acid concentrations were limited to 0.30 M at 25 C, 1.0 M at 40 C, and 3.0 M at 50 C. The data indicate that CMPO extracts nitric acid with a 1:1 stoichiometry. The value of the equilibrium constant is estimated at 2.66 ± 0.09 at 25 C. The enthalpy of the extraction is estimated to be -5.46 ± 0.46 kcal/mol

  7. Intrinsic nitric oxide-stimulatory activity of lipoteichoic acids from different Gram-positive bacteria

    Czech Academy of Sciences Publication Activity Database

    Zídek, Zdeněk; Farghali, H.; Kmoníčková, Eva

    2010-01-01

    Roč. 23, č. 4 (2010), s. 300-310. ISSN 1089-8603 R&D Projects: GA ČR GA305/08/0535 Institutional research plan: CEZ:AV0Z50390512 Keywords : Lipoteichoic acid * Gram-positive bacteria * Nitric oxide Subject RIV: FR - Pharmacology ; Medidal Chemistry Impact factor: 3.384, year: 2010

  8. Dissolution of sludges containing uranium dioxide and metallic uranium in nitric acid

    International Nuclear Information System (INIS)

    The dissolution in nitric acid of sludges containing uranium oxide and uranium has been modeled. That study has shown that it was necessary to continuously feed the dissolver to have an appropriate control of the reaction. If a unique procedure is deemed preferable, NH03 6M has been used

  9. Efficient extraction of Rh(III) from nitric acid medium using a hydrophobic ionic liquid.

    Science.gov (United States)

    Bell, Thomas James; Ikeda, Yasuhisa

    2012-04-21

    Rhodium(III) has been successfully extracted from an aqueous nitric acid solution using a hydrophobic ammonium based ionic liquid and CMPO or TODGA as extractant. This result has significant potential for the recovery of rhodium from spent nuclear fuel and thereby increasing the worldwide supply of this rare metal. PMID:22382888

  10. Method for the manufacture of nitric acid soluble mixed oxide fuel pellets

    International Nuclear Information System (INIS)

    For the manufacture of nitric acid-soluble mixed oxide fuel pellets with adjustable proportions, the starting powder is ground down to a primary grain size of < 2 μm together with a halogen-free grinding aid and subsequently mixed. The change is then granulated in a rotating chamber, pressed into pellet form and sintered. (orig.)

  11. Susceptibility to stress corrosion cracking of zirconium and titanium alloy in nitric acid

    International Nuclear Information System (INIS)

    The susceptibility to stress corrosion cracking (SCC) of zirconium and titanium alloys used in nuclear fuel reprocessing plants was examined by the slow strain rate tensile test (SSRT) in nitric acid solutions by referencing those results obtained in silicone oil. Titanium alloys like Zr-39%Ti, Zr-15%Ti and Zr-5%Ti, Ti-5%Ta were used. Titanium alloys have not the susceptibility to SCC in nitric acid solutions. On the other hand zirconium have the susceptibility to SCC in the same solutions. In comparison with SSRT results of zirconium specimens with a notch in oil, the reduction ratio of time to failure in nitric acid solutions decreased with increasing temperature. The quasi-cleavage type SCC fracture morphology was observed on the fracture surface of specimens tested in nitric acid. In order to evaluate the effect of crystal anisotropy on SCC, L type specimens and C type specimens, which were machined out parallel and perpendicular to the rolling direction respectively were examined. The susceptibility to SCC of C type notched specimens was higher than that of L type notched specimens, because of the preferential texture of quasi-cleavage planes oriented along the cracking path. (author)

  12. Reaction of formaldehyde and nitric acid in a remotely operated thermosiphon evaporator

    International Nuclear Information System (INIS)

    Conditions have been developed for the safe and successful use of a method for reacting formaldehyde with excess nitric acid, while simulataneously concentrating a fissile uranium nitrate solution. This process, which is being conducted in a remotely operated thermosiphon evaporator, has been adapted to plant scale and is being used to process multikilogram batches

  13. Research on the Reaction Between Technetium and Hydrazine in Nitric Acid Medium

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    The reaction between technetium and hydrazine in nitric acid medium was studied by the titration ofthe concentration of hydrazine and pursuing the concentration of heptavalent technetium along with time.It is approved that the reaction between technetium and hydrazine includes an inducing period, a fast

  14. Brightening of the global cloud field by nitric acid and the associated radiative forcing

    Directory of Open Access Journals (Sweden)

    R. Makkonen

    2012-08-01

    Full Text Available Clouds cool Earth's climate by reflecting 20% of the incoming solar energy, while also trapping part of the outgoing radiation. The effect of human activities on clouds is poorly understood, but the present-day anthropogenic cooling via changes of cloud albedo and lifetime could be of the same order as warming from anthropogenic addition in CO2. Soluble trace gases can increase water condensation to particles, possibly leading to activation of smaller aerosols and more numerous cloud droplets. We have studied the effect of nitric acid on the aerosol indirect effect with the global aerosol-climate model ECHAM5.5-HAM2. Including the nitric acid effect in the model increases cloud droplet number concentrations globally by 7%. The nitric acid contribution to the present-day cloud albedo effect was found to be −0.32 W m−2 and to the total indirect effect −0.46 W m−2. The contribution to the cloud albedo effect is shown to increase to −0.37 W m−2 by the year 2100, if considering only the reductions in available cloud condensation nuclei. Overall, the effect of nitric acid can play a large part in aerosol cooling during the following decades with decreasing SO2 emissions and increasing NOx and greenhouse gases.

  15. [Case of dyspnea due to toilet cleaner containing nitric acid for household use].

    Science.gov (United States)

    Yanagawa, Youichi; Matsukawa, Takehisa; Yokoyama, Kazuhito; Hirano, Yohei; Ri, Tetsunari; Aihara, Koichiro; Iba, Toshiaki; Tanaka, Hiroshi

    2013-09-01

    A 40-year-old male tried to clean a urinal at his home storing 900 mL of a toilet cleaner containing 9.8% nitric acid to remove calcium deposit, and clean the toilet floor for twenty minutes. Immediately after using the cleaner, he experienced eye irritation. He washed out the toilet cleaner. However, he thereafter experienced dyspnea, a compressive sensation in his chest, and chest and back pain about 40 minutes after the cleaning the toilet. He monitored his symptoms overnight and found them to gradually improve. However, the symptoms still remained the next morning and therefore he came to our department on foot. He had no particular past or family history. On arrival, his physiological findings and chest computed tomography scan were negative for any abnormalities. His arterial blood gas analysis revealed a mild abnormality of oxygenation. Observation without any drugs revealed that a complete remission of his symptoms occurred after approximately 4 weeks. Based on the results of the experiments, contact with the mucosal membrane and nitric acid gas produced by any accidentally coexisting metals or contact with moisture, including nitric acid produced by a reaction between CaCO3 and cleaner, may have been the mechanism of occurrence for the symptoms observed in this case. This is the first reported case of nitric acid poisoning due to the use of a toilet cleanser intended for household use. PMID:24224389

  16. Extraction of Palladium from Nitric Acid by Diamides of Di-picolinic Acid

    International Nuclear Information System (INIS)

    The most complicated and urgent problem of atomic industry consists in the safe isolation and storage of radioactive wastes. The long-lived radionuclides presented in high-level liquid wastes (HLLW) pose a potential threat to environment for hundreds and thousands of years. One of the possible ways to reduce the danger of HLLW storages is concerned with treatment of HLLW intended to recovery of long-lived radionuclides and their partitioning into separate fractions. The separation of the most hazardous radionuclides (like transplutonium elements (TPE)) to the individual fraction of low volume leads to decrease of the total volume of HLLW and therefore to decrease of solidified waste storage costs. It should be noted that only in the case of reprocessing it can be possible to recover individual radionuclides (or their fractions) into separate flows with further special approach to each of them. Partitioning of different HLLW is under investigation in many countries now. Numerous processes for recovery of Cs, Sr, TPE and REE have been already developed and tested. At the same time partitioning is only the first step on the road to the following synthesis of materials providing the safe storage of long-lived radionuclides over many thousands of years. The metallic palladium contained in HLLW seems to be a promising material for producing of matrices for incorporation of radioactive wastes. Different methods for palladium recovery have been investigated: reductive precipitation, electrochemical precipitation, sorption and extraction. Of prime importance are extraction methods. Phosphine oxides, carbamoyl-phosphine oxides, crown-ethers, oximes, sulfides and some other compounds were proposed as extractants towards palladium from nitric acid media. It is reasonable to recover palladium into individual fraction during waste partitioning. Diamides of malonic, di-glycolic and pyridine-dicarboxylic (di-picolinic) acids are intensively investigated as extractants for HLLW

  17. Tropospheric nitric acid columns from the IASI satellite instrument interpreted with a chemical transport model: Implications for parameterizations of nitric oxide production by lightning

    Science.gov (United States)

    Cooper, Matthew; Martin, Randall V.; Wespes, Catherine; Coheur, Pierre-Francois; Clerbaux, Cathy; Murray, Lee T.

    2014-08-01

    This paper interprets tropical tropospheric nitric acid columns from the Infrared Atmospheric Sounding Interferometer (IASI) satellite instrument with a global chemical transport model (GEOS-Chem). GEOS-Chem and IASI columns generally agree over the tropical ocean to within 10%. However, the GEOS-Chem simulation underestimates IASI nitric acid over Southeast Asia by a factor of 2. The regional nitric acid bias is confirmed by comparing the GEOS-Chem simulation with additional satellite (High Resolution Dynamics Limb Sounder, Atmospheric Chemistry Experiment Fourier Transform Spectrometer) and aircraft (Pacific Exploratory Mission (PEM)-Tropics A and PEM-West B) observations of the middle and upper troposphere. This bias appears to be driven by the lightning NOx parameterization, both in terms of the magnitude of the NOx source and the ozone production efficiency of concentrated lightning NOx plumes. We tested a subgrid lightning plume parameterization and found that an ozone production efficiency of 15 mol/mol in lightning plumes over Southeast Asia in conjunction with an additional 0.5 Tg N would reduce the regional nitric acid bias from 92% to 6% without perturbing the rest of the tropics. Other sensitivity studies such as modified NOx yield per flash, increased altitude of lightning NOx emissions, decreased convective mass flux, or increased scavenging of nitric acid required unrealistic changes to reduce the bias.

  18. Nitric Acid Revamp and Upgrading of the Alarm & Protection Safety System at Petrokemija, Croatia

    Directory of Open Access Journals (Sweden)

    Hoško, I.

    2012-04-01

    Full Text Available Every industrial production, particularly chemical processing, demands special attention in conducting the technological process with regard to the security requirements. For this reason, production processes should be continuously monitored by means of control and alarm safety instrumented systems. In the production of nitric acid at Petrokemija d. d., the original alarm safety system was designed as a combination of an electrical relay safety system and transistorized alarm module system. In order to increase safety requirements and modernize the technological process of nitric acid production, revamping and upgrading of the existing alarm safety system was initiated with a new microprocessor system. The newly derived alarm safety system, Simatic PCS 7, links the function of "classically" distributed control (DCS and logical systems in a common hardware and software platform with integrated engineering tools and operator interface to meet the minimum safety standards with safety integrity level 2 (SIL2 up to level 3 (SIL3, according to IEC 61508 and IEC 61511. This professional paper demonstrates the methodology of upgrading the logic of the alarm safety system in the production of nitric acid in the form of a logical diagram, which was the basis for a further step in its design and construction. Based on the mentioned logical diagram and defined security requirements, the project was implemented in three phases: analysis and testing, installation of the safety equipment and system, and commissioning. Developed also was a verification system of all safety conditions, which could be applied to other facilities for production of nitric acid. With the revamped and upgraded interlock alarm safety system, a new and improved safety boundary in the production of nitric acid was set, which created the foundation for further improvement of the production process in terms of improved analysis.

  19. Thermodynamics and kinetics of thermal decomposition of diamylamyl phosphonate-nitric acid systems

    International Nuclear Information System (INIS)

    Highlights: ► The thermal hazard characteristics of DAAP has been evaluated for the first time. ► The thermodynamic and kinetic parameters have also been derived wherever possible. ► The onset of decomposition of the acid-solvates depended on the nitric acid content. ► A clear trend was seen in the decomposition of acid-solvates of TBP, TiAP and DAAP. - Abstract: Thermal decomposition of neat diamylamyl phosphonate (DAAP), nitric acid-solvates of DAAP and 1.1 M DAAP/n-dodecane was studied calorimetrically in heat-wait-search mode for the first time. The neat DAAP decomposed beyond 500 K while DAAP·0.7HNO3, DAAP·HNO3 and DAAP·2.1HNO3 decomposed exothermally at 386, 381 and 366 K respectively, indicating the role of amount of nitric acid on decomposition. Mixture of DAAP and 8 M nitric acid decomposed at a lower temperature than the acid solvates with a larger excursion in temperature and pressure yielding hydrocarbons, CO2, CO, NOx and a reddish liquid or a black solid residue. Enthalpy of decomposition of DAAP·0.7HNO3, DAAP·HNO3 and DAAP·2.1HNO3 were found to be −237.7 ± 4.8, −348.9 ± 3.4 and −1002.1 ± 2.6 kJ mol−1 and the activation energy and pre-exponential factors were 127.5 ± 1.5, 121.8 ± 0.8 and 105.3 ± 1.2 kJ mol−1 and 9.0 × 1013, 1.4 × 1012 and 2.2 × 1010 lit mol−1 s 1, respectively. Heat capacity (Cp) of acid solvates were measured and used for deriving the enthalpy change.

  20. Bile acid induced colonic irritation stimulates intracolonic nitric oxide release in humans.

    OpenAIRE

    F. Casellas; Mourelle, M; Papo, M; Guarner, F; Antolin, M; Armengol, J R; J. R. Malagelada

    1996-01-01

    AIM--To measure the intracolonic release of nitric oxide end products (nitrates plus nitrites) and eicosanoids in response to intraluminal irritation with deoxycholic acid (DCA). PATIENTS--Seven patients with irritable bowel syndrome. METHODS--The left colon was perfused with a solution with or without 3 mM deoxycholic acid. Aspirates were assayed for eicosanoids by specific radioimmuno-assay, and for nitrates plus nitrites by the Griess reaction. To confirm that stimulated colonic mucosa can...

  1. Corrosion res ance of stainless steels in media of nitric-acid decomposition of apatite

    International Nuclear Information System (INIS)

    Presented are results of investigation of corrosion resistance of stainless steels 06KhN28MDT, 08Kh21N6M2T, 08Kh22N5T and Kh18N10T in media initiating composition of pulp liquid phase of nitric acid decompositon of apatite (phosphoric acid, hydrofluoric acid and fluosilicic acid). Principle application possibility of economically-alloyed as to nickel the 08Kh21N62MT steels for the apparatus equipment of the process instead of highly alloyed 06KhN28MDT steel is established

  2. Modification of cation-exchange properties of activated carbon by treatment with nitric acid

    International Nuclear Information System (INIS)

    The uptake of inorganic cations by high-surface-area activated carbon can be increased by an order of magnitude by controlled exposure to high concentrations of nitric acid at elevated temperatures. Distribution coefficients of cations are also increased. Oxidation treatment causes some loss in particle strength. Acid strength of the functional groups from the nitric acid treatment is greater than those of the starting material. Surface area measurements from small-angle neutron scattering indicate that the increase in effective ion-exchange capacity is not accompanied by gross changes in the structure of the material. 13C-NMR on solid samples suggests that the concentration of carboxyl and phenolic functional groups in the carbon is increased by the treatment

  3. Improvement in electrochemical capacitance of activated carbon from scrap tires by nitric acid treatment

    Science.gov (United States)

    Han, Yan; Zhao, Ping-Ping; Dong, Xiao-Ting; Zhang, Cui; Liu, Shuang-Xi

    2014-12-01

    Activated carbon (AC) obtained from the industrial pyrolytic tire char is treated by concentrated nitric acid (AC-HNO3) and then used as the electrode material for supercapacitors. Surface properties and electrochemical capacitances of AC and ACHNO3 are studied. It is found that the morphology and the porous texture for AC and AC-HNO3 have little difference, while the oxygen content increases and functional groups change after the acid treatment. Electrochemical results demonstrate that the AC-HNO3 electrode displays higher specific capacitance, better stability and cycling performance, and lower equivalent series resistance, indicating that AC obtained from the industrial pyrolytic tire char treated by concentrated nitric acid is applicable for supercapacitors.

  4. Plutonium (4) and neptunium (4) extraction with tributyl phosphate from solutions containing nitric and formic acids

    International Nuclear Information System (INIS)

    Distribution of Pu(4) and Np(4) between 30% solution of tributyl phosphate in dodecane and aqueous solutions containing nitric and formic (HFm) acids has been studied. It is shown that during coextraction of nitric and formic acids mixed solvates in organic phase are not formed. It is established that Pu(4) and Np(4) are reextracted into aqueous phase, containing formic acid at the expense of both displacing and complexing effect of HFm. Equations describing the dependence of concentrational constants of Pu(4) and Np(4) extraction on the content of HNO3 and HFm in aqueous phase are obtained. The equations can be used for mathematical modelling of Pu(4) and Np(4) distribution in the extractional processes

  5. Flotation-nitric acid leach procedure for increasing uranium recovery from a refractory ore

    International Nuclear Information System (INIS)

    The Bureau of Mines investigated a flotation-nitric acid leach procedure as part of the goal to maximize minerals and metals recovered from primary and secondary domestic resources. Studies were conducted on an ore that contained carbon-bearing and sulfide mineralization that rendered a portion of the ore refractory (resistant) to conventional leaching technology. The procedure investigated for treating the ore consisted of the following: (1) separation by flotation of the carbonaceous and sulfidic components from the ore, (2) leaching the flotation concentrate with nitric acid at 1000 to 1100C, (3) leaching the flotation tailings with sulfuric acid, and (4) processing the combined leached slurries in a conventional manner to recover yellow cake. In step 2, HNO3 is converted to gaseous products from which it is regenerated by reacting these products with air and water for further leaching. An overall uranium extraction of 96% was achieved by this procedure

  6. The influence of nitric acid on the cloud processing of aerosol particles

    Directory of Open Access Journals (Sweden)

    S. Romakkaniemi

    2006-01-01

    Full Text Available In this paper we present simulations of the effect of nitric acid (HNO3 on cloud processing of aerosol particles. Sulfuric acid (H2SO4 production and incloud coagulation are both affected by condensed nitric acid as nitric acid increases the number of cloud droplets, which will lead to smaller mean size and higher total surface area of droplets. As a result of increased cloud droplet number concentration (CDNC, the incloud coagulation rate is enhanced by a factor of 1–1.3, so that the number of interstitial particles reduces faster. In addition, sulfuric acid production occurs in smaller particles and so the cloud processed aerosol size distribution is dependent on the HNO3 concentration. This affects both radiative properties of aerosol particles and the formation of cloud droplets during a sequence of cloud formation-evaporation events. It is shown that although the condensation of HNO3 increases the number of cloud droplets during the single updraft, it is possible that presence of HNO3 can actually decrease the cloud droplet number concentration after several cloud cycles when also H2SO4 production is taken into account.

  7. Recovery of nitric acid from simulated acidic high level radioactive waste using pore-filled anion exchange membranes

    International Nuclear Information System (INIS)

    Acidic waste is generated at different stages of nuclear fuel cycle. The waste contains minor amounts of actinides (241Am, Pu, Np) along with large number of long-lived radionuclides such as 137Cs, 90Sr, 106Ru etc. Before disposal or storage, the overall activity of the waste needs to be reduced. Along with this, the high amount of acid present in the waste needs to be removed. In this study, DD has been used to recover nitric acid from acidic solutions with compositions similar to radioactive waste using pore-filled anion exchange membranes

  8. Changes of Petroleum Acid Distribution Characterized by FT-ICR MS in Heavy Acidic Crude Oil after True Boiling Point Distillation

    Institute of Scientific and Technical Information of China (English)

    Liu Yingrong; Zhang Qundan; Wang Wei; Liu Zelong; Zhu Xinyi; Tian Songbai

    2014-01-01

    The molecular transformations of carboxylic acids in heavy acidic SL crude before and after true boiling point distillation were examined by ultra-high resolution negative-ion electrospray ionization (ESI) Fourier transform ion cyclo-tron resonance mass spectrometry (FT-ICR MS). The acid class (heteroatom number), type (z numbers) and carbon number distributions were positively characterized. It was found out that the total acid number (TAN) of SL crude decreased after true boiling point distillation, and the abundance of O2 class in mass spectra was also found to be reduced from 67.6%to 34.5%in SL TBP mixed crude as measured by MS spectra, indicating to a potential carboxylic acid decomposition. However, it was interesting that the carboxylic acids type distribution in both oils was almost the same although their relative abundance in SL TBP mixed crude turned to be much lower, suggesting that various petroleum carboxylic acid types have the similar thermal decomposition reaction behavior. Furthermore, for each O2 type of acids in SL TBP mixed crude, the abundance of carboxylic acids with carbon number higher than 35 was reduced greatly, especially for those with carbon number higher than 60, the mass peaks of which were nearly totally removed, indicating that the large carboxylic acid molecules in heavy fractions decomposed more signiifcantly because of longer heating time during the true boiling point distillation process. As a result, the reduction of TAN may be caused by the thermal decomposition of carboxylic acids especially those with high carbon number, suggesting that quick distillation or much lower pressure is required to avoid the thermal decomposition.

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

    International Nuclear Information System (INIS)

    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 CO2. 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

  10. Studies on the sorption of Pu(IV) on alumina microspheres from nitric acid - oxalic acid solutions

    International Nuclear Information System (INIS)

    Sorption of Pu(IV) on alumina microspheres prepared by the sol-gel procedure has been investigated for the recovery of plutonium from nitric acid-oxalic acid solutions. Distribution ratio for Pu(IV) between alumina microspheres and nitric acid-oxalic acid have been determined. The influence of the mode of preparation and heat treatment of these microspheres, on the sorption of Pu(IV) have been investigated. Pu(IV) breakthrough capacities have been determined using a 5 ml bed of alumina with solutions of Pu(IV) in 1M HNO3 + 0.05M H2C2O4 and 0.5M HNO3 + 0.05M H2C2O4. The elution behavior of Pu(IV) loaded on these microspheres were studied using nitric acid solutions containing different oxidising and reducing agents. Investigations were also carried out to fix the activity in the alumina matrix by heat treatment. (author)

  11. Determination of plutonium in nitric acid solution by spectrophotometry of Pu(VI), (2)

    International Nuclear Information System (INIS)

    Effects of co-existing agent and of Pu(IV)-polymer formation on the oxidation of Pu(IV) to Pu(VI) by Ce(IV) has been investigated in connection with the spectrophotometric determination of plutonium in nitric acid solution which includes the measurement of absorbance at 833 nm due to Pu(VI) after oxidizing plutonium ion into Pu(VI). Hydrogen peroxide and nitrite ions were dealt with as interfering species because these are most main radiolysis products in nitric acid solution. If 4 times or more concentration of Ce(IV) than that of hydrogen peroxide or nitrite ion is added to the sample solution, plutonium ion can be converted to Pu(VI) quantitatively even in the presence of these agents. Plutonium(IV) forming its polymer is hard to be oxidized to Pu(VI) by Ce(IV). The oxidation rate of Pu(IV)-polymer increases with the increase of the acid concentration of the solution. It takes, however, more than 1 hour to attain complete oxidation of polymer into Pu(VI) even in 3 M nitric acid solution. (author)

  12. Nitric Acid-Treated Carbon Fibers with Enhanced Hydrophilicity for Candida tropicalis Immobilization in Xylitol Fermentation

    Directory of Open Access Journals (Sweden)

    Le Wang

    2016-03-01

    Full Text Available Nitric acid (HNO3-treated carbon fiber (CF rich in hydrophilic groups was applied as a cell-immobilized carrier for xylitol fermentation. Using scanning electron microscopy, we characterized the morphology of the HNO3-treated CF. Additionally, we evaluated the immobilized efficiency (IE of Candida tropicalis and xylitol fermentation yield by investigating the surface properties of nitric acid treated CF, specifically, the acidic group content, zero charge point, degree of moisture and contact angle. We found that adhesion is the major mechanism for cell immobilization and that it is greatly affected by the hydrophilic–hydrophilic surface properties. In our experiments, we found 3 hto be the optimal time for treating CF with nitric acid, resulting in an improved IE of Candida tropicalis of 0.98 g∙g−1 and the highest xylitol yield and volumetric productivity (70.13% and 1.22 g∙L−1∙h−1, respectively. The HNO3-treated CF represents a promising method for preparing biocompatible biocarriers for multi-batch fermentation.

  13. Flow boiling critical heat flux enhancement on the 2-D slice for boric acid and TSP solution

    International Nuclear Information System (INIS)

    The critical heat flux (CHF) on the reactor vessel external wall was measured using the small scale two-dimensional slice test section. The radius of the curvature and the channel area of the test section were 0.15 m and 0.03 mx0.03 m, respectively. The objectives are to assess the effects of additives (TSP, boric acid) and heated material (SA508) in inclination angle 90° and to investigate flow boiling CHF enhancement resulting from various working fluids of 5000 ppm tri-sodium phosphate (TSP, Na3PO4∙12H2O) solution, 4000 ppm boric acid solution and mixture solution of TSP and boric acid. Boric acid solution didn't show CHF enhancement and TSP and mixture solution showed CHF enhancement (20~34%). (author)

  14. Easy synthesis of graphene sheets from alfalfa plants by treatment of nitric acid

    Energy Technology Data Exchange (ETDEWEB)

    Qu, Jiao, E-mail: qujiao@bhu.edu.cn [School of Chemistry and Chemical Engineering, Bohai University, Jinzhou 121013 (China); School of Urban and Environmental Sciences, Northeast Normal University, Changchun 130024 (China); Luo, Chunqiu, E-mail: fplj_lcq@163.com [School of Chemistry and Chemical Engineering, Bohai University, Jinzhou 121013 (China); Zhang, Qian; Cong, Qiao [School of Chemistry and Chemical Engineering, Bohai University, Jinzhou 121013 (China); Yuan, Xing [School of Urban and Environmental Sciences, Northeast Normal University, Changchun 130024 (China)

    2013-04-01

    Highlights: ► An easy method for synthesis of graphene sheets using alfalfa plants was introduced. ► An novelty formation mechanism of graphene sheets using alfalfa plants was proposed. ► This method exploits a new carbon source and provides a novel idea to synthesize graphene sheets. -- Abstract: This letter focuses on synthesis of graphene sheets from alfalfa plants by treatment of nitric acid. The transmission electron microscopy image (TEM) demonstrates that the graphene sheets are agglomerated and overlapped, the energy dispersive spectrum (EDS) indicates that the products are pure, and the Raman spectrum shows the graphene sheets are well graphitized. In addition, the formation mechanism of the graphene sheets from alfalfa plants by treatment nitric acid is discussed. These findings inspire the search for a new strategy for synthesis of graphene sheets from renewable natural products, and the lower cost of this new process and carbon source may facilitate industrial production.

  15. Fractionation of microimpurities during precipitation of basic zirconium sulfate out of nitric acid solutions

    International Nuclear Information System (INIS)

    A study was made on fractionation of microimpurities during precipitation of basic zirconium sulfate out of concentrated with respect to ZrO2 nitric acid solutions. Investigation into fractionation of Sc(3), Cr(3), Mn(2), Fe(3), Co(2), CU(2), Zn(2) and Y(3) microirpurities during hydrolytic precipitation of basic zirconium sulfate out of nitric acid solutions showed that a majority of microimpurities are characterized by high distribution factors and concentrate in mother liquor. Adsorption isotherms were constructed for Cu(2) and Fe(3) microimpurities. The assumption about the effect of microimpurity nature (ionic charge and radius, the electron structure) on precipitation mechanism was made on the base of obtained data

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2000-09-28

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

  17. Easy synthesis of graphene sheets from alfalfa plants by treatment of nitric acid

    International Nuclear Information System (INIS)

    Highlights: ► An easy method for synthesis of graphene sheets using alfalfa plants was introduced. ► An novelty formation mechanism of graphene sheets using alfalfa plants was proposed. ► This method exploits a new carbon source and provides a novel idea to synthesize graphene sheets. -- Abstract: This letter focuses on synthesis of graphene sheets from alfalfa plants by treatment of nitric acid. The transmission electron microscopy image (TEM) demonstrates that the graphene sheets are agglomerated and overlapped, the energy dispersive spectrum (EDS) indicates that the products are pure, and the Raman spectrum shows the graphene sheets are well graphitized. In addition, the formation mechanism of the graphene sheets from alfalfa plants by treatment nitric acid is discussed. These findings inspire the search for a new strategy for synthesis of graphene sheets from renewable natural products, and the lower cost of this new process and carbon source may facilitate industrial production

  18. Passive Sampler for Measurements of Atmospheric Nitric Acid Vapor (HNO3 Concentrations

    Directory of Open Access Journals (Sweden)

    Andrzej Bytnerowicz

    2001-01-01

    Full Text Available Nitric acid (HNO3 vapor is an important nitrogenous air pollutant responsible for increasing saturation of forests with nitrogen and direct injury to plants. The USDA Forest Service and University of California researchers have developed a simple and inexpensive passive sampler for monitoring air concentrations of HNO3. Nitric acid is selectively absorbed on 47-mm Nylasorb nylon filters with no interference from particulate NO3-. Concentrations determined with the passive samplers closely corresponded with those measured with the co-located honeycomb annular denuder systems. The PVC protective caps of standardized dimensions protect nylon filters from rain and wind and allow for reliable measurements of ambient HNO3 concentrations. The described samplers have been successfully used in Sequoia National Park, the San Bernardino Mountains, and on Mammoth Mountain in California.

  19. Investigation on surface structure of potassium permanganate/nitric acid treated poly(tetrafluoroethylene)

    Science.gov (United States)

    Fu, Congli; Liu, Shuling; Gong, Tianlong; Gu, Aiqun; Yu, Zili

    2014-10-01

    In the previous articles concerning the treatment of poly(tetrafluoroethylene) (PTFE) with potassium permanganate/nitric acid mixture, the conversion of a hydrophobic to a hydrophilic surface was partially assigned to the defluorination of PTFE and then the introduction of carbonyl and hydroxyl groups into the defluorinated sites. In the present work, PTFE sheets were treated with potassium permanganate/nitric acid, and the surfaces before and after treatment were comparatively characterized by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The surface sediments of the treated PTFE were also determined by atomic absorption spectroscopy (AAS). The results indicate that the conversion of the hydrophobicity to the hydrophilicity on the modified PTFE surface is mainly due to the deposition of hydrophilic manganese oxides which covered the fluorocarbon surface, and no detectable chemical reactions of PTFE occur in the treating process.

  20. Effect of carrier concentration on transportation of thorium from nitric acid medium across supported liquid membrane using Aliquat 336 as carrier

    International Nuclear Information System (INIS)

    Thorium transportation across supported liquid membrane from nitric acid as a function of carrier concentration and feed acidity is studied. Thorium transportation increased with nitric acid concentration till 5 M feed acidity and decreased after wards. Thorium permeability coefficient varies greatly as a function of carrier concentration depending on the feed acidity conditions. (author)

  1. Photosynthetic and growth responses of Schima superba seedlings to sulfuric and nitric acid depositions.

    Science.gov (United States)

    Yao, Fang-Fang; Ding, Hui-Ming; Feng, Li-Li; Chen, Jing-Jing; Yang, Song-Yu; Wang, Xi-Hua

    2016-05-01

    A continuing rise in acid deposition can cause forest degradation. In China, acid deposition has converted gradually from sulfuric acid deposition (SAD) to nitric acid deposition (NAD). However, the differing responses of photosynthesis and growth to depositions of sulfuric vs. nitric acid have not been well studied. In this study, 1-year-old seedlings of Schima superba, a dominant species in subtropical forests, were treated with two types of acid deposition SO4 (2-)/NO3 (-) ratios (8:1 and 0.7:1) with two applications (foliar spraying and soil drenching) at two pH levels (pH 3.5 and pH 2.5) over a period of 18 months. The results showed that the intensity, acid deposition type, and spraying method had significant effects on the physiological characteristics and growth performance of seedlings. Acid deposition at pH 2.5 via foliar application reduced photosynthesis and growth of S. superba, especially in the first year. Unlike SAD, NAD with high acidity potentially alleviated the negative effects of acidity on physiological properties and growth, probably due to a fertilization effect that improved foliar nitrogen and chlorophyll contents. Our results suggest that trees were damaged mainly by direct acid stress in the short term, whereas in the long term, soil acidification was also likely to be a major risk to forest ecosystems. Our data suggest that the shift in acid deposition type may complicate the ongoing challenge of anthropogenic acid deposition to ecosystem stability. PMID:26797956

  2. Search for an in-line nitric acid analyzer

    Energy Technology Data Exchange (ETDEWEB)

    Gallagher, K. Y.; Johnson, C. M.

    1980-10-01

    A literature search was conducted to identify possible techniques for measuring mineral acid normality in the presence of heavy metal salts, undissolved solids, and high radiation fields. Of the techniques noted, eight were identified that could be applicable to the objective. The possibilities were reduced to two methods, which warrant further investigation. These two are refractometry and a modified coulometric-polarographic method. All methods are discussed in detail followed by rationale for including or rejecting each for further investigation.

  3. Search for an in-line nitric acid analyzer

    International Nuclear Information System (INIS)

    A literature search was conducted to identify possible techniques for measuring mineral acid normality in the presence of heavy metal salts, undissolved solids, and high radiation fields. Of the techniques noted, eight were identified that could be applicable to the objective. The possibilities were reduced to two methods, which warrant further investigation. These two are refractometry and a modified coulometric-polarographic method. All methods are discussed in detail followed by rationale for including or rejecting each for further investigation

  4. Radiolysis studies of uranyl nitrate solution in nitric acid medium

    International Nuclear Information System (INIS)

    The radiolysis of acidic uranyl nitrate solutions was investigated using Co-60 gamma radiation. Hydrogen peroxide was determined as a function of increasing dose. The UV-vis absorption spectra of the irradiated solutions were measured and the spectral changes were analyzed. The increasing dose increases the absorbance intensities, possibly by an increment in nitrate concentration produced by radiolysis, which can originate the formation of different uranyl complexes in solution. (author)

  5. Study on the Reaction Between Methyl Hydrazine and Formaldehyde in Nitric Acid Medium

    Institute of Scientific and Technical Information of China (English)

    LI; Chuan-bo; CAO; Zhi; BIAN; Xiao-yan; XIAN; Liang; YAN; Tai-hong; ZHENG; Wei-fang

    2012-01-01

    <正>To make sure whether the reaction between formaldehyde and methyl hydrazine (MMH) could happen in dilute nitric acid solution, the condensation reaction between the two ones was investigated at 16 ℃. The reaction was slow and it took over 5 hours to reach the balance and the solution turned yellow at last. The maximum absorption peaks of the product existed at 340 nm and 400-450 nm, respectively.

  6. Pb(II) leaching from waste CRT funnel glass in nitric acid solutions

    OpenAIRE

    A. Strzałkowska; M. Wojtala; J. Siwka

    2012-01-01

    Purpose: The paper presents experimental results of Pb (II) leaching from waste CRT funnel glass using solution of nitric acid (V) . This work focused on examining the impact of concentration and particle size on the leaching percentage of Pb (II) from funnel glass.Design/methodology/approach: Material for the investigation was crushed and sieved. Leaching was carried out using working solutions pfrom co repared ncentrated HNO3 and mechanical stirrer.Findings: The received results show the po...

  7. Comparison of anion exchange resins for recovering plutonium from nitric acid waste

    International Nuclear Information System (INIS)

    Microreticular and macroreticular anion exchange resins were compared for their capability of recovering plutonium from nitric acid waste streams. Plutonium breakthrough capacity and elution behavior of the resins were determined as a function of resin properties. Small-bead microreticular resins with a polystyrene matrix containing 4% divinylbenzene cross-linkage showed the best performance. Of the 20- to 50-mesh resins, the macroreticular resin, Amberlite IRA-938, gave the highest plutonium breakthrough capacity and eluted plutonium the fastest

  8. Nitric Acid Revamp and Upgrading of the Alarm & Protection Safety System at Petrokemija, Croatia

    OpenAIRE

    Hoško, I.; Zečević, N.; Pavlaković, S.

    2012-01-01

    Every industrial production, particularly chemical processing, demands special attention in conducting the technological process with regard to the security requirements. For this reason, production processes should be continuously monitored by means of control and alarm safety instrumented systems. In the production of nitric acid at Petrokemija d. d., the original alarm safety system was designed as a combination of an electrical relay safety system and transistorized alarm module system. I...

  9. Procedure of Destructive Chemical Recovery of Precious Metals in Nitric Acid Production

    OpenAIRE

    Ljubičić, M.; Zečević, N.

    2012-01-01

    The heart of the nitric acid production process is the chemical reactor containing a platinum-based catalyst pack and an associated catchment system, which allows the ammonia oxidation reaction to take place efficiently. Under the severe operating conditions imposed by the high-pressure ammonia oxidation process, the catalyst gauzes experience progressive deterioration, as shown by the restricted surface of the catalyst wires, the loss of catalytic activity and the loss of catalytic materials...

  10. Trans Fatty Acids Induce Vascular Inflammation and Reduce Vascular Nitric Oxide Production in Endothelial Cells

    OpenAIRE

    Iwata, Naomi G.; Pham, Matilda; Rizzo, Norma O.; Cheng, Andrew M.; Maloney, Ezekiel; Kim, Francis

    2011-01-01

    Intake of trans fatty acids (TFA), which are consumed by eating foods made from partially hydrogenated vegetable oils, is associated with a higher risk of cardiovascular disease. This relation can be explained by many factors including TFA's negative effect on endothelial function and reduced nitric oxide (NO) bioavailability. In this study we investigated the effects of three different TFA (2 common isomers of C18 found in partially hydrogenated vegetable oil and a C18 isomer found from rumi...

  11. Autoclave leaching of molybdenite concentrates with catalytic additives of nitric acid

    Science.gov (United States)

    Smirnov, K. M.; Raspopov, N. A.; Shneerson, Ya. M.; Lapin, A. Yu.; Bitkov, G. A.; Men'shikov, Yu. A.; Paskhin, P. N.; Kirichenko, V. P.

    2010-07-01

    The scientific theoretical prerequisites for the use of small additives of nitric acid for the intensification of the autoclave oxidative leaching (AOL) of sulfide concentrates are checked in order to increase the degree of extraction of the base metal with a simultaneous decrease in the cost of the process. The technological parameters of the AOL conditions applied to molybdenite are also refined, and recommendations for a practical application of the apparatus of the process and for a decrease in its cost are made.

  12. Effect of Nitric Acid Concentrations on Synthesis and Stability of Maghemite Nanoparticles Suspension

    OpenAIRE

    Irwan Nurdin; Mohd Rafie Johan; Iskandar Idris Yaacob; Bee Chin Ang

    2014-01-01

    Maghemite (γ-Fe2O3) nanoparticles have been synthesized using a chemical coprecipitation method at different nitric acid concentrations as an oxidizing agent. Characterization of all samples performed by several techniques including X-ray diffraction (XRD), transmission electron microscopy (TEM), alternating gradient magnetometry (AGM), thermogravimetric analysis (TGA), dynamic light scattering (DLS), and zeta potential. The XRD patterns confirmed that the particles were maghemite. The crysta...

  13. Effects of composite restorations on nitric oxide and uric acid levels in saliva

    OpenAIRE

    Nilgun Akgul; Pinar Gul; Hamit Hakan Alp; Ahmet Kiziltunc

    2015-01-01

    Background and Aims: Dental materials that are used in dentistry should be harmless to oral tissues, and should, therefore, not contain any leachable toxic and diffusible substances capable of causing side effects. This study was intended to investigate the effects on salivary nitric oxide (NO) and uric acid (UA) levels after application of dental composite filling materials to healthy volunteers. Materials and Methods: A total of 52 individuals (32 female and 20 male) participated in the stu...

  14. Heterogeneous formation of polar stratospheric clouds – Part 1: Nucleation of nitric acid trihydrate (NAT)

    OpenAIRE

    C. R. Hoyle; I. Engel; Luo, B. P.; Pitts, M.C.; Poole, L. R.; Grooß, J.-U.; Peter, T

    2013-01-01

    Satellite-based observations during the Arctic winter of 2009/2010 provide firm evidence that, in contrast to the current understanding, the nucleation of nitric acid trihydrate (NAT) in the polar stratosphere does not only occur on preexisting ice particles. In order to explain the NAT clouds observed over the Arctic in mid-December 2009, a heterogeneous nucleation mechanism is required, occurring via immersion freezing on the surface of solid particles, likely of meteoriti...

  15. Heterogeneous formation of polar stratospheric clouds – Part 1: Nucleation of nitric acid trihydrate (NAT)

    OpenAIRE

    C. R. Hoyle; I. Engel; Luo, B. P.; Pitts, M.C.; Poole, L. R.; J.-U. Grooß; Peter, T

    2013-01-01

    Satellite based observations during the Arctic winter of 2009/2010 provide firm evidence that, in contrast to the current understanding, the nucleation of nitric acid trihydrate (NAT) in the polar stratosphere does not only occur on preexisting ice particles. In order to explain the NAT clouds observed over the Arctic in mid December 2009, a heterogeneous nucleation mechanism is required, occurring via immersion freezing on the surface of solid particles, likely of meteoritic origin. For t...

  16. Investigation of scandium nitrate-nitric acid-water-tributylphosphate system. 1. Scandium extraction isotherms

    International Nuclear Information System (INIS)

    Distribution of scandium between 100% tbp and 0.2-1.2 mole/l scandium in the 2.7-12.3 mole/l nitric acid is investigated. It is shown that Sc extracts in undiluted tbp, equilibrium with 6-12 mole/l HNO3, contain approximately from one to five molecules pro atom of scandium in the extracted Sc-complex. 14 refs.; 2 figs

  17. Extraction behaviour of Am(III) and Eu(III) from nitric acid medium in CMPO-HDEHP impregnated resins

    Energy Technology Data Exchange (ETDEWEB)

    Saipriya, K.; Kumar, T. [Bhabha Atomic Research Centre Facilities (India). Kalpakkam Reproscessing Plants; Kumaresan, R.; Nayak, P.K.; Venkatesan, K.A.; Antony, M.P. [Indira Gandhi Center for Atomic Research, Kalpakkam (India). Fuel Chemistry Div.

    2016-05-01

    Chromatographic resin containing extractants such as octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO) or bis-(2-ethylhexyl)phosphoric acid (HDEHP) or mixture of extractants (CMPO + HDEHP) in an acrylic polymer matrix was prepared and studied for the extraction of Am(III) and Eu(III) over a range of nitric acid concentration. The effect of various parameters such as concentration of nitric acid in aqueous phase and the concentration of CMPO and HDEHP in the resin phase was studied. The distribution coefficient of Am(III) and Eu(III) in the impregnated resin increased with increased in the concentration of nitric acid for CMPO-impregnated resin, whereas a reverse trend was observed in HDEHP impregnated resin. In case of resin containing both the extractants, synergism was observed at low nitric acid concentration and antagonism at high nitric acid concentration. The mechanism of extraction was probed by slope analysis method at 0.01 and 2 M nitric acid concentrations. Citrate-buffered DTPA was used for the selective separation of Am(III), and a separation factor of 3-4 was obtained at pH 3.

  18. Permeation behavior of yttrium from nitric acid medium with DNPPA in hollow fibre membrane module

    International Nuclear Information System (INIS)

    High purity yttrium finds applications in superconductors, phosphors, as additives in alloys, in cancer treatment, etc. Monazite mineral contains ∼ 4% yttrium apart from other rare earths. Its separation from the leach solution obtained from processing monazite is primarily done by solvent extraction using di 2-ethyl hexyl phosphoric acid (D2EHPA) and 2-ethyl hexyl 2-ethyl hexyl phosphonic acid (EHEHPA) as extractants. Recently, use of di nonyl phenyl phosphoric acid (DNPPA) in separating metal ions from highly acidic solution has gained importance due to its low pKa value (2.54). It is worth exploring DNPPA for rare earth separation from acidic solutions. Amongst various separation techniques, hollow fibre membrane offer low capital and operating cost, low energy, solvent inventory and high concentration factors. In the present investigation an attempt has been made to study the permeation behavior of Y (III) from nitric acid medium in a hollow fibre supported liquid membrane (HFSLM) module with DNPPA as carrier

  19. Oxidation and degradation of short-chain aliphatic compounds by hyperazeotropic nitric acid

    International Nuclear Information System (INIS)

    To determine the ultimate fate of organic material present in nuclear fuel reprocessing solutions and the chemical nature of the last surviving residues, organic products of the hydrolysis/nitrolysis of tributyl phosphate were subjected to further degradation with boiling 20 M HNO3 (Iodox Process) and carbon balances were run. Except for methyl nitrate, nitrate esters were oxidized in refluxing 20 M HNO3, primarily to a mixture of carbon dioxide and the corresponding and shorter chain aliphatic acids. Typically, 40% or more of the carbon from the nitrate esters was converted to CO2. Except for formic acid, the straight-chain monobasic acids oxidized slowly. Compounds identified among those resulting from oxidation of butyric acid (e.g., from the oxidation of butyl nitrate) included succinic and oxalic acids, 3- and 4-hydroxy-butyric acids, nitrate esters of 3- and 4-hydroxybutyric acid, butyrolactone, and 3-nitrobutyric acid. The mechanisms for formation of these products are briefly discussed. Oxalic acid and the hydroxyaliphatic acids have some potential for complexing ceertain metallic fission products. These results show that traces of organic materials will always be present in actual fuel processing solutions unless special measures are taken to ensure their removal. This conclusion was reinforced by analysis of recycle acid from the Savannah River Plant. The possible implications to a reprocessing plant using 100% recycle are briefly discussed

  20. Extraction and Separation of Lanthanum (III) and Neodymium (III) from Nitric acid by Aliquat-336 in Kerosene

    International Nuclear Information System (INIS)

    Aliquat-336 (tricapryl methyl ammonium chloride) in kerosene was used as an extractant for La (Ill) and Nd (Ill) from nitric acid medium. The different parameters affecting the extraction of the investigated metal ions such as hydrogen ion concentration, nitric acid, Aliquat-336 concentration, metal ion, loading capacity as well as temperature were separately investigated. The extraction of both cations was found to increase with increasing Aliquat-336, metal ion, nitrate and nitric acid concentration, while it decreases slightly with hydrogen ion concentration. The stoichiometry of the extracted metal species investigated was found to be M (NO3)-4L+ for both cations. The thermodynamic functions were determined and discussed. The stripping of the extracted metal species by nitric, sulphuric, hydrochloric acids and sodium hydroxide were carried out. The difference in the extraction and stripping conditions was used for the separation of La (III) and Nd (Ill) from aqueous nitrate medium.

  1. Amide functionalized Calix-Benzocrown-6 ionophore for extraction of cesium from highly concentrated nitric acid medium

    International Nuclear Information System (INIS)

    A series of novel calix(4)arene-benzocrown-6 amide (CBCA) ligands in 1,3-alternate conformations with amidic group attached to aromatic ring of the polyether ring network have been synthesised and evaluated for extraction of caesium from nitric acid medium (1-10M). Isodecyl alcohol (IDA) and o-nitrophenyl hexyl ether (o-NPHE) modified calix/dodecane have been used for extraction studies. The extraction of Cs increases with nitric acid concentration, the maxima is obtained at ∼ 4.5M for calix-benzo-crown-6 (CBC) used as standard, whereas, in case of CBCA this maxima reaches to ∼ 8M nitric acid concentration. This difference is attributed to neutralization of nitric acid by intramolecular buffering effect of amidic group of CBCA. (author)

  2. Kinetics of Reaction Between Tc(Ⅶ) and Monomethylhydrazine or Dimethylhydroxylamine in Nitric Acid Medium Containing Plutonium

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    <正>The chemical reaction kinetics research of Tc(Ⅶ) with monomethylhydrazine or dimethylhydroxy-lamine in nitric acid medium demonstrated that Tc(Ⅶ) hardly reacts with the salt-free reagents during the

  3. Application of Primary Abatement Technology for Reduction of N2O Emmision in Petrokemija Nitric Acid Production

    OpenAIRE

    Ćosić, L.; Zečević, N.

    2013-01-01

    Industrial nitric acid production by oxidation of gaseous ammonia with Ostwald procedure produces an unwanted by-product – colorless nitrous oxide, N2O. As emission of N2O represents a very serious problem due of its huge contribution to global warming, certain measures focused on its maximum reduction should be undertaken. Minimization of N2O emission in nitric acid production can be achieved in different parts of the process flow, depe...

  4. Chemical reaction calculation simulation of redox behavior of metal ions and the like in the nitric acid solution

    International Nuclear Information System (INIS)

    It is known that corrosion rate of stainless steel in nitric acid solution is affected by the valence change of oxidizing metallic ions. In this study, we conducted redox reaction analyses using chemical reaction calculation model to clarify the mechanism of valence change. We obtained that the oxidization of metallic ions in the solution is not only caused by nitric acid but also nitrogen oxides. (author)

  5. Extraction of uranium (VI) and thorium (IV) ions from nitric acid solutions by N.N.N'.N'-tetrabutylsuccinylamiide

    International Nuclear Information System (INIS)

    Solvent extraction of U(VI) and Th(IV) from nitric acid medium by N.N.N'.N'-tetrabutylsuccinylamide(TBSA) in a diluent composed of 50% trimethyl benzene (TMB) and 50% kerosene(OK) is described. Extraction coefficients of U(VI) and Th(IV) as a function of aqueous nitric acid concentration, extractant concentration and temperature have been studied. From the data, the compositions of extracted species, equilibrium constants and enthalpies of extraction reaction are also been calculated

  6. 4.2. The kinetics of nitric acid decomposition of calcined borosilicate raw material of Ak-Arkhar Deposit

    International Nuclear Information System (INIS)

    Present article is devoted to kinetics of nitric acid decomposition of calcined borosilicate raw material of Ak-Arkhar Deposit. The dependence of nitric acid decomposition of calcined boric raw material for extraction of boron oxide on temperature (20-100 deg C) and process duration (15-60 minutes) was defined. It was defined that at temperature increasing the extraction rate of boron oxide increases from 20.8 to 78.6%.

  7. Boils (Furunculosis)

    Science.gov (United States)

    ... boil starts to drain, wash the area with antibacterial soap and apply some triple antibiotic ointment and a ... avoid spreading the infection to others. Use an antibacterial soap on boil-prone areas when showering, and dry ...

  8. The solubility of thorium fluoride in nitric acid-hydrofluoric acid solution between 25 and 1000C

    International Nuclear Information System (INIS)

    The solubility of thorium fluoride in 4, 8, and 13 M nitric acid solutions was measured as a function of fluoride concentration at 25, 50 and 1000C. The behavior of the solubility is best explained by the existence in solution of the species ThFsub(n)sup((4-n)+), where n has values between 0 and 4. Equilibrium quotients for the stepwise complexation of thorium by fluoride are calculated. (author)

  9. Novel amino acids: synthesis of furoxan and sydnonimine containing amino acids and peptides as potential nitric oxide releasing motifs.

    Science.gov (United States)

    Nortcliffe, Andrew; Botting, Nigel P; O'Hagan, David

    2013-07-28

    The incorporation of furoxan and sydnonimine ring systems into amino acid side chains is demonstrated with the preparation of four novel amino acids which carry these nitric oxide-releasing motifs. N-((4-Nitrophenoxy)carbonyl)-3-phenylsydnonimine 9 and bis(phenylsulfonyl)furoxan 10 are the key intermediates for introducing the heterocycle side chains onto appropriate amine and alcohol functionalities respectively. Furoxan 5 and 7 both displayed NO release based on determination of nitrite production. Orthogonal amino acid protecting group strategies were deployed to demonstrate that the amino acids could be incorporated into peptide frameworks. By way of demonstration the amino acids were placed centrally into several tripeptide motifs. Griess test assays showed that these amino acids released NO in the presence of γ-glutathione (GST). PMID:23753002

  10. Sulfuric, hydrochloric, and nitric acid-catalyzed triacetone triperoxide (TATP) reaction mixtures: an aging study.

    Science.gov (United States)

    Fitzgerald, Mark; Bilusich, Daniel

    2011-09-01

    The organic peroxide explosive triacetone triperoxide (TATP) is regularly encountered by law enforcement agents in various stages of its production. This study utilizes solid-phase microextraction (SPME) and gas chromatography/mass spectrometry (GC/MS) to examine sulfuric acid-, hydrochloric acid-, and nitric acid-catalyzed TATP syntheses during the initial 24 h of these reactions at low temperatures (5-9°C). Additionally, aging of the reaction mixtures was examined at both low and ambient temperatures (19-21°C) for a further 9 days. For each experiment, TATP could be readily identified in the headspace above the reaction mixture 1 h subsequent to the combination of reagents; at 24 h, TATP and diacetone diperoxide (DADP) were prominent. TATP degraded more rapidly than DADP. Additionally, chlorinated acetones chloroacetone and 1,1,-dichloroacetone were identified in the headspace above the hydrochloric acid-catalyzed TATP reaction mixture. These were not present when the catalyst was sulfuric acid or nitric acid. PMID:21595692

  11. Dissolution of thorium/uranium mixed oxide in nitric acid-hydrofluoric acid solution

    International Nuclear Information System (INIS)

    The dissolution process of thorium oxide and mixed uranium-thorium oxide is studied, as a step of the head-end of the fuel reprocessing. An extensive bibliography was analysed, concerning the main aspects of the system, specially the most important process variables. Proposed mechanisms and models for the thorium oxide dissolution are presented. The laboratory tests were performed in two phases: at first, powdered thoria was used as the material to be dissolved. The objective was to know how changes in he concentrations of the dissolvent solution components HNO3, HF and Al(NO3)3 affect the dissolution rate. The tests were planned according to the fractional factorial method. Thes results showed that it is advantageous to work with powdered material, since the reaction occurs rapidly. And, if the Thorex solution (HNO3 13M, HF 0.05M and Al(NO3)3 0.10M) is a suitable dissolvent, it was verified that it is possible to reduce the concentration of either nitric or fluoridric acid, without reducing the reaction rate to an undesirable value. It was also observed significant interaction between the components of the dissolvent solution. In the second phase of the tests, (Th, 5%U)O2 sintered pellets were used. The main goals were to know the pellets dissolution behaviour and to compare the results for different pellets among themselves. It was observed that the metallurgical history of the material strongly influences its dissolution, specially the density and the microstructure. It was also studied how the (Th,U)O2 mass/Thorex solution volume ratio affects the time needed to obtain an 1 M Th/liter solution. The activation energy for the reaction was obtained. (Author)

  12. Supercritical fluid extraction of uranium and thorium from nitric acid medium using organophosphorous compounds

    Energy Technology Data Exchange (ETDEWEB)

    Pitchaiah, K.C.; Sujatha, K.; Rao, C.V.S. Brahmmananda; Subramaniam, S.; Sivaraman, N.; Rao, P.R. Vasudeva [Indira Gandhi Centre for Atomic Research, Kalpakkam (India). Chemistry Group

    2015-06-01

    In recent years, Supercritical Fluid Extraction (SFE) technique has been widely used for the extraction of metal ions. In the present study, extraction of uranium from nitric acid medium was investigated using supercritical carbon dioxide (Sc-CO{sub 2}) containing various organophosphorous compounds such as trialkyl phosphates e.g. tri-iso-amyl phosphate (TiAP), tri-sec-butyl phosphate (TsBP) and tri-n-butyl phosphate (TBP), dialkylalkyl phosphonates, e.g. diamylamyl phosphonate (DAAP) and dibutyl butyl phosphonate (DBBP), dialkyl hydrogen phosphonates, e.g. dioctyl hydrogen phosphonate (DOHP), dioctylphosphineoxide (DOPO), trioctyl phosphine oxide (TOPO), n-octylphenyl N,N-diisobutyl carbamoylmethylphosphine oxide (CMPO) and di-2-ethyl-hexyl phosphoric acid (HDEHP). Some of these ligands have been investigated for the first time in the supercritical phase for the extraction of uranium. The extraction efficiency of uranium was studied with TiAP, DAAP and DBBP as a function of nitric acid concentration; the kinetics of the equilibration period (static extraction) and transportation of the metal complex (dynamic extraction) was investigated. The influence of pressure and temperature on the extraction behaviour of uranium with DAAP was studied from 4 N HNO{sub 3}. The extraction efficiency of uranium from 4 N nitric acid medium was found to increase in the order of phosphates < phosphonates < HDEHP < TOPO < CMPO. In the case of phosphates and phosphonates, the maximum extraction of uranium was found to be from 4 N HNO{sub 3} medium. The acidic extractants, HDEHP and DOHP showed relatively higher extraction at lower acidities. The relative extraction of uranium and thorium from their mixture was also examined using Sc-CO{sub 2} containing phosphates, phosphonates and TOPO. The ligand, TsBP provided better fractionation between uranium and thorium compared to trialkyl phosphates, dialkyl alkyl phosphonates and TOPO.

  13. Supercritical fluid extraction of uranium and thorium from nitric acid medium using organophosphorous compounds

    International Nuclear Information System (INIS)

    In recent years, Supercritical Fluid Extraction (SFE) technique has been widely used for the extraction of metal ions. In the present study, extraction of uranium from nitric acid medium was investigated using supercritical carbon dioxide (Sc-CO2) containing various organophosphorous compounds such as trialkyl phosphates e.g. tri-iso-amyl phosphate (TiAP), tri-sec-butyl phosphate (TsBP) and tri-n-butyl phosphate (TBP), dialkylalkyl phosphonates, e.g. diamylamyl phosphonate (DAAP) and dibutyl butyl phosphonate (DBBP), dialkyl hydrogen phosphonates, e.g. dioctyl hydrogen phosphonate (DOHP), dioctylphosphineoxide (DOPO), trioctyl phosphine oxide (TOPO), n-octylphenyl N,N-diisobutyl carbamoylmethylphosphine oxide (CMPO) and di-2-ethyl-hexyl phosphoric acid (HDEHP). Some of these ligands have been investigated for the first time in the supercritical phase for the extraction of uranium. The extraction efficiency of uranium was studied with TiAP, DAAP and DBBP as a function of nitric acid concentration; the kinetics of the equilibration period (static extraction) and transportation of the metal complex (dynamic extraction) was investigated. The influence of pressure and temperature on the extraction behaviour of uranium with DAAP was studied from 4 N HNO3. The extraction efficiency of uranium from 4 N nitric acid medium was found to increase in the order of phosphates < phosphonates < HDEHP < TOPO < CMPO. In the case of phosphates and phosphonates, the maximum extraction of uranium was found to be from 4 N HNO3 medium. The acidic extractants, HDEHP and DOHP showed relatively higher extraction at lower acidities. The relative extraction of uranium and thorium from their mixture was also examined using Sc-CO2 containing phosphates, phosphonates and TOPO. The ligand, TsBP provided better fractionation between uranium and thorium compared to trialkyl phosphates, dialkyl alkyl phosphonates and TOPO.

  14. Extraction of nitric acid, technetium and palladium by bidentate carbamoylphosphonates

    Energy Technology Data Exchange (ETDEWEB)

    Gorski, B.; Kuca, L.; Petrzilova, H.

    1985-09-01

    The extraction of HNOsub(3), TcOsub(4)sup(-), and Pd by solutions of dibutyl N,N-diethylcarbomylmethylenephosphonate (DBDECMP) and dibutyl N,N-diethylcarbamoylphosphonate (DBDECP) in CClsub(4) was studied. At low aqueous acidities, HNOsub(3) is extracted by both extractants (S) as HNOsub(3) x S and HNOsub(3)xSsub(2), at > IM HNOsub(3) only HNOsub(3)xS is formed. The distribution of TcOsub(4)sup(-) and Pd(II) is nearly independent of HNOsub(3) concentration. A second power dependence on extractant concentration was found for the extraction of Pd(II) by DBDECMP and TcOsub(4)sup(-) by DBDECP, and a 4th power dependence for TcOsub(4)sup(-) - DBDECMP. (author). 9 refs.; 7 figs.

  15. The influence of temperature on REE and TPE sorption by sulfocation exchangers from nitric acid solutions

    International Nuclear Information System (INIS)

    Data of numerical and physical experiments on rare earths sorption from nitric acid solutions on the KU-2 sulfocationite, depending on temperature, are presented. It is shown that capacity in terms of europium at the temperature of 70 deg C for solutions with acidity exceeding 1.0 mol/l and in the range of europium concentrations 0.023-0.0428 mol/l increases by 20-30%. At increased temperature the width of sorptional front increases significantly. The calculated data are isomorphous to sorption process observed in the experiment. 4 refs.; 3 figs.; 2 tabs

  16. Supercritical fluid extraction of uranium from nitric acid employing crown ether

    International Nuclear Information System (INIS)

    Selective extraction and separation of uranium from various matrices is imperative due to its importance as nuclear fuel material. Supercritical fluid extraction of uranium from nitric acid medium employing CO2 as supercritical fluid and di-tert-butyldibenzo-18-crown-6 as co-solvent has been investigated. PFOA was employed as counter ion. Effects of various parameters e.g. pressure, temperature, time of extraction, acidity of medium, metal-to-crown and crown- to-counter ion ratio, on extraction efficiency were examined. Under optimized condition, an extraction efficiency of (58±5)% was obtained. (author)

  17. Electrochemical behaviour of niobium and niobium passive films in nitric acid solutions

    International Nuclear Information System (INIS)

    Electrochemical behaviour of bare niobium and phosphoric acid anodized niobium electrodes is investigated in nitric acid solutions. Electrochemical impedance spectroscopy and polarisation techniques have been used to investigate the open-circuit growth of the passive film. The stability of the anodic oxide film has been studied as a function of the formation voltage, formation current density and concentration of the ambient electrolyte. The results show that the Nb-Nb2O5-1M HNO3 does not behave as a perfect dielectric. The flat band potential and donor concentration of the semiconducting anodic oxide film have been calculated from the Mott-Schottky plots. (author)

  18. Solvent Extraction of Zr(IV) from Nitric Acid Solutions using CYANEX 272, CYANEX 301 and CYANEX 302

    International Nuclear Information System (INIS)

    The extraction of Zr(IV) from nitric acid solutions using CYANEX 272 (bis(2,4,4-trimethylpentyl) phosphinic acid), bis (2,4,4-trimethylpentyl) dithio phosphinic acid (CYANEX 301) or (bis(2,4,4-trimethylpentyl) mono phosphinic acid (CYANEX 302) in kerosene has been investigated. The various factors affecting the extraction process of Zr(IV) by each of the investigated extractants such as contact time, loading capacity, extractant, metal ion and nitric acid concentration as well as temperature, are separately investigated. The stripping of the extracted zirconium from loaded organic solutions is also carried out using different stripping reagents. The results are compared and the potential advantages of each extractant over the others are exploited in terms of higher loading capacity and selectivity, less nitric acid extraction, equilibration period and reagent concentration

  19. Monohydroxamic acids and bridging dihydroxamic acids as chelators to ruthenium(III) and as nitric oxide donors: syntheses, speciation studies and nitric oxide releasing investigations.

    Science.gov (United States)

    Griffith, Darren; Krot, Krystyna; Comiskey, Jedd; Nolan, Kevin B; Marmion, Celine J

    2008-01-01

    The synthesis and spectroscopic characterisation of novel mononuclear Ru(III)(edta)(hydroxamato) complexes of general formula [Ru(H2edta)(monoha)] (where monoha = 3- or 4-NH2, 2-, 3- or 4-C1 and 3-Me-phenylhydroxamato), as well as the first example of a Ru(III)-N-aryl aromatic hydroxamate, [Ru(H2edta)(N-Me-bha)].H2O (N-Me-bha = N-methylbenzohydroxamato) are reported. Three dinuclear Ru(III) complexes with bridging dihydroxamato ligands of general formula [{Ru(H2edta)}2(mu-diha)] where diha = 2,6-pyridinedihydroxamato and 1,3- or 1,4-benzodihydroxamato, the first of their kind with Ru(III), are also described. The speciation of all of these systems (with the exception of the Ru-1,4-benzodihydroxamic acid and Ru-N-methylbenzohydroxamic systems) in aqueous solution was investigated. We previously proposed that nitrosyl abstraction from hydroxamic acids by Ru(III) involves initial formation of Ru(III)-hydroxamates. Yet, until now, no data on the rate of nitric oxide (NO) release from hydroxamic acids has been published. We now describe a UV-VIS spectroscopic study, where we monitored the decrease in the ligand-to-metal charge-transfer band of a series of Ru(III)-monohydroxamates with time, with a view to gaining an insight into the NO-releasing properties of hydroxamic acids. PMID:18399240

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-03-13

    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.

  1. Effect of nitric acid on pretreatment and fermentation for enhancing ethanol production of rice straw.

    Science.gov (United States)

    Kim, Ilgook; Lee, Bomi; Park, Ji-Yeon; Choi, Sun-A; Han, Jong-In

    2014-01-01

    In this study, nitric acid (HNO₃) was evaluated as an acid catalyst for rice straw pretreatment, and, after neutralization, as a sole nitrogen source for subsequent fermentation. Response surface methodology was used to obtain optimal pretreatment condition with respect to HNO₃ concentration (0.2-1.0%), temperature (120-160 °C) and reaction time (1-20 min). In a condition of 0.65% HNO₃, 158.8 °C and 5.86 min, a maximum xylose yield of 86.5% and an enzymatic digestibility of 83.0% were achieved. The sugar solution that contained nitrate derived from the acid catalyst supported the enhancement of ethanol yield by Pichia stipitis from 10.92 g/L to 14.50 g/L. The results clearly reveal that nitric acid could be used not only as a pretreatment catalyst, but also as a nitrogen source in the fermentation process for bioethanol production. It is anticipated that the HNO₃-based pretreatment can reduce financial burden on the cellulosic bioethanol industry by simplifying after-pretreatment-steps as well as providing a nitrogen source. PMID:24274544

  2. Nitric Acid Dehydration Using Perfluoro Carboxylate and Mixed Sulfonate/Carboxylate Membranes

    Energy Technology Data Exchange (ETDEWEB)

    R.L. Ames

    2004-09-01

    Perfluoro ionomer membranes are tetrafluoro ethylene-based materials with microheterogeneous structures consisting of a hydrophobic polymer backbone and a hydrophilic side-chain cluster region. Due to the ionomer cluster morphology, these films exhibit unique transport properties. Recent investigations with perfluoro sulfonate and perfluoro sulfonate/carboxylate composite polymers have demonstrated their value in the dehydration of nitric acid and they show potential as an alternative to conventional, energy intensive unit operations in the concentration of acid feeds. As a result, investigations were conducted to determine the feasibility of using pure perfluoro carboxylate and mixed perfluoro sulfonate/carboxylate films for the dehydration of nitric acid because of the speculation of improved water selectivity of the carboxylate pendant chain. During the first phase of these investigations the effort was focused on generating a thin, solution cast perfluoro carboxylate ionomer film, to evaluate the general, chemical and physical characteristics of the polymer, and to assess the material's aqueous transport performance (flux and nitrate separation efficiencies) in pervaporation and high-pressure environments. Results demonstrated that generating robust solution-cast films was difficult yet a number of membranes survived high trans-membrane pressures up to 700 psig. General characterization of the solution cast product showed reduced ion exchange capacities when compared with thicker, ''as received'' perfluoro carboxylate and similar sulfonate films. Small angle x-ray scattering analysis results suggested that the solution cast carboxylate films contained a small fraction of sulfonate terminated side-chains. Aqueous transport experimentation showed that permeate fluxes for both pure water and nitric acid were approximately two orders of magnitude smaller for the carboxylate solution cast membranes when compared to their sulfonate

  3. Estimation of the Production of Ozone and Nitric Acid in a Proton Accelerator Facility of the Proton Engineering Frontier Project

    International Nuclear Information System (INIS)

    The operation of the high-energy particle accelerator leads to the production of not only radioactive gases, but also radiolytic noxious gases, such as ozone and nitrogen compounds in the air of the facility. Of the radiolytic products, ozone production is usually taken into account for the evaluation of the heath hazard in the operation of the particle accelerator facilities, owing to its high radiolytic yield and much lower maximum acceptable concentration. Nitrogen compounds do not commonly constitute a heath hazard but are of important concern because of its chemical properties of being a strong acid and a strong oxidizing agent. Among the nitrogen compounds, nitric acid is a principal radiolytic compound produced in large quantities and has a potential for the corrosion of the components in the facility. It has founded that at a high-energy proton accelerator facility, nitric acid was produced in the radiolysis of air in beam-loss region. The nitric acid was desorbed on the surface of the magnet, walls, floors and local lead shields. It also tends to be more uniform through the tunnel due to air circulation. In these backgrounds, the production of ozone and nitric acid in proton accelerator facility from Proton Engineering Frontier Project (PEFP) was estimated in this study, because very strong radiation environment leads to an abundant production of nitric acid in such a high-current proton accelerator

  4. Trans fatty acids induce vascular inflammation and reduce vascular nitric oxide production in endothelial cells.

    Directory of Open Access Journals (Sweden)

    Naomi G Iwata

    Full Text Available Intake of trans fatty acids (TFA, which are consumed by eating foods made from partially hydrogenated vegetable oils, is associated with a higher risk of cardiovascular disease. This relation can be explained by many factors including TFA's negative effect on endothelial function and reduced nitric oxide (NO bioavailability. In this study we investigated the effects of three different TFA (2 common isomers of C18 found in partially hydrogenated vegetable oil and a C18 isomer found from ruminant-derived-dairy products and meat on endothelial NF-κB activation and nitric oxide (NO production. Human endothelial cells were treated with increasing concentrations of Elaidic (trans-C18:1 (9 trans, Linoelaidic (trans-C18:2 (9 trans, 12 trans, and Transvaccenic (trans-C18:1 (11 trans for 3 h. Both Elaidic and Linoelaidic acids were associated with increasing NF-κB activation as measured by IL-6 levels and phosphorylation of IκBα, and impairment of endothelial insulin signaling and NO production, whereas Transvaccenic acid was not associated with these responses. We also measured superoxide production, which has been hypothesized to be necessary in fatty acid-dependent activation of NF-κB. Both Elaidic acid and Linoelaidic acid are associated with increased superoxide production, whereas Transvaccenic acid (which did not induce inflammatory responses did not increase superoxide production. We observed differential activation of endothelial superoxide production, NF-κB activation, and reduction in NO production by different C18 isomers suggesting that the location and number of trans double bonds effect endothelial NF-κB activation.

  5. Assessing the Parameterization of Nitric Oxide Emissions By Lightning in a Chemical Transport Model with Nitric Acid Columns from the IASI Satellite Instrument

    Science.gov (United States)

    Cooper, M.; Martin, R.; Wespes, C.; Coheur, P. F.; Clerbaux, C.; Murray, L. T.

    2014-12-01

    Nitrogen oxides (NOx ≡ NO + NO2) in the free troposphere largely control the production of ozone (O3), an important greenhouse gas and atmospheric oxidant. As HNO3 is the dominant sink of tropospheric NOx, improved understanding of its production and loss mechanisms can help to better constrain NOx emissions, and in turn improve understanding of ozone production and its effect on climate. However, this understanding is inhibited by the scarcity of direct measurements of free tropospheric HNO3, particularly in the tropics. We interpret tropical tropospheric nitric acid columns from the IASI satellite instrument with a global chemical transport model (GEOS-Chem). Overall GEOS-Chem generally agrees with IASI, however we find that the simulation underestimates IASI nitric acid over Southeast Asia by a factor of two. The bias is confirmed by comparing the GEOS-Chem simulation with additional satellite (HIRDLS, ACE-FTS) and aircraft (PEM-Tropics A and PEM-West B) observations of the middle and upper troposphere. We show that this bias can be explained by the parameterization of lightning NOx emissions, primarily from the misrepresentation of concentrated subgrid lightning NOx plumes. We tested a subgrid lightning plume parameterization and found that an additional 0.5 Tg N with an ozone production efficiency of 15 mol/mol would reduce the regional nitric acid bias from 92% to 6% without perturbing the rest of the tropics. Other sensitivity studies such as modified NOx yield per flash, increased altitude of lightning NOx emissions, or changes to convective mass flux or wet deposition of nitric acid required unrealistic changes to reduce the bias. This work demonstrates the importance of a comprehensive lightning parameterization to constraining NOx emissions.

  6. Temperature and composition effect on the volumic masses of uranium and plutonium nitric acid solutions

    International Nuclear Information System (INIS)

    With an oscillating U-tube densimeter, we measured at different temperatures the volumic masses of uranium, plutonium and nitric acid solutions. By multiple linear regression analysis we found the representative equation of the different parameters in fluence on the volumic mass. We have obtained from the tabulated data the representative equation of the pure water between 15 and 400C with a better precision than 2.10-5g.cm-3. From our own results we have obtained the equations concerning the nitric acid between 0 and 8 M at 200C, then between 15 and 400C. The agreement with our experimental results and with the tabulated data at 200C is in some 10-4g.cm-3 range. At last the general equation which comprises the above found terms is in concordance with the experimental results in +- 1,2.10-3g.cm-3 bracket in the scanned range (200C 0C - 2 M 3] -1 -1 - 1 gl-1 -1). Nevertheless we are not able to explain the difference of 2,3.10-3 g.cm-3 between the constant term of this equation and the choosed origin (the volumic mass of the pure water at 200C). The variations observed between our results and these determined in other laboratories for two constituents systems may be explain by errors in free acidity measurements where these is still no complete agreement between laboratories

  7. Evaluation of various Crown ethers for the supercritical fluid extraction of uranium from nitric acid medium

    International Nuclear Information System (INIS)

    Various crowns have been evaluated for supercritical fluid extraction of uranium from nitric acid medium employing HPFOA as counter ion. Uranium extraction efficiency was found to be influenced by cavity size of crown ether and nature of substituents. Complexation tendency of UO22+ increases with increasing cavity size of crown ether. Electron withdrawing substituents decreased the extraction efficiency which could be attributed to decrease in the basicity of four oxygen atoms and hence their bonding ability. Whereas electron donating substituents increased the efficiency due to increases in basicity of oxygen atoms and hence in increase in bonding ability. (author)

  8. Nitric oxide functions in both methyl jasmonate signaling and abscisic acid signaling in Arabidopsis guard cells

    OpenAIRE

    Saito, Naoki; Nakamura, Yoshimasa; Mori, Izumi C.; Murata, Yoshiyuki

    2009-01-01

    Intracellular components in methyl jasmonate (MeJA) signaling remain largely unknown, to compare those in well-understood abscisic acid (ABA) signaling. We have reported that nitric oxide (NO) is a signaling component in MeJA-induced stomatal closure, as well as ABA-induced stomatal closure in the previous study. To gain further information about the role of NO in the guard cell signaling, NO production was examined in an ABA- and MeJA-insensitive Arabidopsis mutant, rcn1. Neither MeJA nor AB...

  9. Thermal decomposition studies on tri-iso-amyl phosphate in n-dodecane-nitric acid system

    International Nuclear Information System (INIS)

    Tri-iso-amyl Phosphate (TiAP) is a promising alternative solvent to TBP, with near similar extraction behaviour and physical properties but lower aqueous phase solubility and does not form third phase during the extraction of Pu(IV). In addition to the solubilised extractant, inadvertent entrainment of the extractant into the aqueous stream is a concern during the evaporation operation as the extractant comes into contact with higher nitric acid concentrations and metal nitrates. Hence the thermal decomposition behaviour of TiAP-HNO3 systems has been studied using an adiabatic calorimeter in closed air ambience, under heat-wait-search mode (H-W-S)

  10. Hypergolic Burning of Formylidene and Furfurylidene amines with Red Fuming Nitric Acid as Oxidizer

    Directory of Open Access Journals (Sweden)

    S. P. Panda

    1977-04-01

    Full Text Available Six p-formylidene and six p-furfurylideneamines were synthesized and their ignition delay with red fuming nitric acid (RFNA were measured by cup test method using a high speed camera. Structure - hypergolicity correlation revealed that a p-methyl group inhibits hypergolicity whereas a p-methoxy group accelerates it. Similarly oxidizable non-conjugated benzene rings increase hypergolicity whereas conjugated benzene rings decrease it. On compacting, the p-formylidene anisidine was found to be hypergolic with an ignition delay less than 100 milliseconds.

  11. Direct Synthesis of Phenol from Benzene on an Activated Carbon Catalyst Treated with Nitric Acid

    Institute of Scientific and Technical Information of China (English)

    Cui-hong Chen; Jia-quan Xu; Ming-ming Jin; Gui-ying Li; Chang-wei Hu

    2011-01-01

    Commercially available coal-based activated carbon was treated by nitric acid with different concentrations and the resultant samples were used as catalysts for the direct hydroxylation of benzene to phenol in acetonitrile. Boehm titration, X-ray photoelectron spectroscopy,scanning electron microscope coupled with an energy dispersive X-ray microanalyzer, and Brunauer-Emmett-Teller method were used to characterize toe samples. The number of carboxyl groups on the surface was found to be the main factor affecting the catalytic activity. An optimum catalytic performance with a yield of 15.7% and a selectivity of 87.2% to phenol was obtained.

  12. Rocket Performance of Red Fuming Nitric Acid with Blends of Norbornadiene, Carene and Cardanol

    OpenAIRE

    R. Chhibber; C. Prabhakaran; Kulkarni, S. G.; S.P. Panda

    1992-01-01

    The fuel blends of nornornadiene and carene (50:50 by weight) and norbornadiene, carene and cardanol (40:40:20 by weight) exhibit synergistic hypergolic ignition with red fuming nitric acid (RFNA) as oxidiser. These fuel blends have been evaluated by theoretical calculations of performance parameters and subsequently verified by static firing in a 10 kg/sub f/ thruster at a chamber pressure of around 20 atm, using RFNA (with 21 per cent N/sub 2/O/sub 4/ by weight) as oxidiser. The theo...

  13. Determination of U(VI) and Pu(IV) in nitric acid solutions with derivative spectroscopy

    International Nuclear Information System (INIS)

    The authors study the absorption spectra and fourth derivative spectra (FDS) of U(VI) and Pu(IV) in nitric acid solutions and the effect of impurities on FDS. The concentrations of U(VI) and Pu(IV) with peak-zero method at 415 nm and peak-area method between 472.5-479.5 nm are determined, respectively. When CHNO3 or CNO3- is in 1.5-3.0 mol/l, U(VI) can be directly determined by FDS, with the analysis deviation -4 mol/l

  14. Study of immiscibilities in the trilaurylamine - dodecane - nitric acid - plutonium system

    International Nuclear Information System (INIS)

    Phase equilibrium in systems made up of trilaurylamine, dodecane, nitric acid tetravalent plutonium is shown by drawing the triangular diagrams. the study of these diagrams provides informations concerning the causes of immiscibility. Heterogeneity of the organic mixtures can be related to some characteristics of the components- dipole moment, molecular polarizability and hydrogen bond exchanging ability-Depending on these, some rules may be established which can be used to make a proper choice of an additive in order to improve the miscibility. As an application a study on the partial substitution of dodecane with decalin, in plutonium extraction experiments, has been done showing a possible improvement of the extraction process. (author)

  15. Supercritical fluid extraction of uranium and thorium from nitric acid solutions with organophosphorus reagents

    International Nuclear Information System (INIS)

    Extraction techniques for the recovery of uranium and transuranic elements from acid waste solutions are important in nuclear waste management. This paper examines the feasibility of extracting uranyl and thorium ions from nitric acid solutions with supercritical CO2 containing the different organophosphorus reagents. In this study, an organophosphorus reagent is dissolved in supercritical CO2 by passing the fluid through a reagent vessel placed upstream of the sample vessel in the extractor. Using TBPO or TOPO in supercritical CO2, effective extraction of uranyl and thorium ions can be achieved even in dilute HNO3 solutions, thus yielding the possibility of reducing acidic waste volumes in nuclear waste treatment. The results may form the basis of a novel extraction process for the treatment of acidified nuclear wastes, while minimizing the production of secondary wastes. 12 refs., 2 figs., 2 tabs

  16. Transport of uranium from nitric acid solution by non-dispersive solvent extraction using a hollow fiber contactor

    International Nuclear Information System (INIS)

    Transport behaviour of uranium from nitric acid medium was investigated using hollow fiber non-dispersive extraction technique. The effect of feed acidity and carrier concentration was studied in counter current mode at a feed flow rate of 3.5 mL/s and an organic phase flow rate of 4.5 mL/s. (author)

  17. Distribution coefficient correlations for nitric acid, U(VI) and Pu(IV) in two-phase system with aqueous nitric acid and 30% tri-n-butylphosphate solutions

    International Nuclear Information System (INIS)

    Distribution coefficient correlations are obtained for nitric acid, U(VI) and Pu(IV) extracted with 30% tri-n-butylphosphate (TBP) diluted by n-dodecane from aqueous nitric acid solutions. The correlation functions are described as a mathematical model that takes account of activity coefficients expressed by a function of ionic strength. The correlations include the temperature effect on distribution coefficient, and works successfully for the experimental distribution coefficients in the literature within the temperature range of 10 to 70degC. The concentrations of nitric acid, U(VI) and Pu(IV) in a multi-stage extraction experiment previously reported have been simulated well with the new distribution correlations at room and elevated temperatures. (author)

  18. Anode material selection criteria for selective oxidation of inorganic compounds in nitric acid media

    International Nuclear Information System (INIS)

    Significant progress has been made since the 19606 in developing highly effective anode materials for electrochemical processes, The problem areas currently facing electrochemistry researchers include investigating new composite materials obtained by grafting or doping, improving fabrication techniques to extend the lifetime of the materials while maintaining their selectivity, studying their electrochemical properties and relating them to the material structure. Research on materials with high oxygen over-potentials-materials on which water oxidation is kinetically affected, and which open an electro-activity window on high potentials (2.0 VESH or greater) - has opened new avenues such as the use of various metallic oxide deposits. Two oxide classes were identified from a structural standpoint on the basis of their water oxidation properties: chemisorbed active oxygen anodes (e.g. PtOx, IrO2 or RuO2) and physi-sorbed active oxygen anodes (e.g. SnO2 or PbO2). Selective electrochemical generation of powerful oxidants between 1.4 and 2.0 VESH in concentrated nitric acid media is used in the context of the nuclear fuel cycle, and the potential advantages of new materials with a high oxygen over-potential-other than widely used platinum-have attracted attention. The relevant physical, chemical and electrochemical properties of such materials were therefore investigated to assess their selective oxidation performance. The study focused in particular on identifying the specific aspects of concentrated nitric acid media in the processes occurring at the electrode/solution interface, using linear and cyclic voltammetry, imposed-potential electrolysis and impedance spectroscopy. This approach allowed characterization of the electron charge transfer kinetics of the medium (nitric acid, compared with other acids such as methane sulfonic acid) and of the selected redox couple (Ag(II)/Ag(I) in this case). The tests covered a wide range of materials, including IrO2, SnO2, PbO2

  19. Procedure of Destructive Chemical Recovery of Precious Metals in Nitric Acid Production

    Directory of Open Access Journals (Sweden)

    Ljubičić, M.

    2012-07-01

    Full Text Available The heart of the nitric acid production process is the chemical reactor containing a platinum-based catalyst pack and an associated catchment system, which allows the ammonia oxidation reaction to take place efficiently. Under the severe operating conditions imposed by the high-pressure ammonia oxidation process, the catalyst gauzes experience progressive deterioration, as shown by the restricted surface of the catalyst wires, the loss of catalytic activity and the loss of catalytic materials. The higher the pressure of gaseous ammonia oxidation, the greater the loss of platinum group metals from the surface of the applied selective heterogeneous catalysts. Total losses for one batch over the whole period of using selective heterogeneous catalysts may account in the range from 20 to 40 % of the total installed quantity of precious metals. An important part of the platinum removed from the platinum-rhodium alloy wires can be recovered at the outlet of the reactor by means of palladium catchment gauzes. However, this catchment process, which is based on the great ability of palladium to alloy with platinum, is not 100 % effective and a fraction of the platinum and practically all of the rhodium lost by the catalyst wires, evades the catchment package and is then deposited in other parts of the plant, especially heat exchangers. From the above mentioned operating equipment, the retained mass of precious metals can be recovered by the technical procedure of non-destructive and destructive chemical solid-liquid extraction.Shown is the technical procedure of destructive chemical recovery of preheater and boiler for preheating and production of steam by applying sulfuric acid (w = 20 % and subsequent procedure of raffination of derived sludge, to the final recovery of precious metals. The technical procedure of destructive chemical recovery of precious metals from preheater and boiler for preheating and production of steam in nitric acid production is

  20. Single-cycle method for partitioning of trivalent actinides using completely incinerable reagents from nitric acid medium

    Energy Technology Data Exchange (ETDEWEB)

    Ravi, Jammu; Venkatesan, K.A.; Antony, M.P.; Srinivasan, T.G.; Rao, P.R. Vasudeva [Indira Gandhi Centre for Atomic Research, Kalpakkam (India). Fuel Chemistry Div.

    2014-10-01

    A new approach, namely 'Single-cycle method for partitioning of Minor Actinides using completely incinerable ReagenTs' (SMART), has been explored for the separation of Am(III) from Eu(III) present in nitric acid medium. The extraction behavior of Am(III) and Eu(III) in a solution of an unsymmetrical diglycolamide, N,N,-didodecyl-N',N'-dioctyl-3-oxapentane-1,5-diamide (D{sup 3}DODGA), and an acidic extractant, N,N-di-2-ethylhexyl diglycolamic acid (HDEHDGA), in n-dodecane was studied. The distribution ratio of both these metal ions in D{sup 3}DODGA-HDEHDGA/n-dodecane initially decreased with increase in the concentration of nitric acid reached a minimum at 0.1 M nitric acid followed by increase. Synergic extraction of Am(III) and Eu(III) was observed at nitric acid concentrations above 0.1 M and antagonism at lower acidities. Contrasting behavior observed at different acidities was probed by the slope analysis of the extraction data. The study revealed the involvement of both D{sup 3}DODGA and HDEHDGA during synergism and increased participation of HDEHDGA during antagonism. The stripping behavior of Am(III) and Eu(III) from the loaded organic phase was studied as a function of nitric acid, DTPA, and citric acid concentrations. The conditions needed for the mutual separation of Am(III) and Eu(III) from the loaded organic phase were optimized. Our studies revealed the possibility of separating trivalent actinides from HLLW using these completely incinerable reagents. (orig.)

  1. Single-cycle method for partitioning of trivalent actinides using completely incinerable reagents from nitric acid medium

    International Nuclear Information System (INIS)

    A new approach, namely 'Single-cycle method for partitioning of Minor Actinides using completely incinerable ReagenTs' (SMART), has been explored for the separation of Am(III) from Eu(III) present in nitric acid medium. The extraction behavior of Am(III) and Eu(III) in a solution of an unsymmetrical diglycolamide, N,N,-didodecyl-N',N'-dioctyl-3-oxapentane-1,5-diamide (D3DODGA), and an acidic extractant, N,N-di-2-ethylhexyl diglycolamic acid (HDEHDGA), in n-dodecane was studied. The distribution ratio of both these metal ions in D3DODGA-HDEHDGA/n-dodecane initially decreased with increase in the concentration of nitric acid reached a minimum at 0.1 M nitric acid followed by increase. Synergic extraction of Am(III) and Eu(III) was observed at nitric acid concentrations above 0.1 M and antagonism at lower acidities. Contrasting behavior observed at different acidities was probed by the slope analysis of the extraction data. The study revealed the involvement of both D3DODGA and HDEHDGA during synergism and increased participation of HDEHDGA during antagonism. The stripping behavior of Am(III) and Eu(III) from the loaded organic phase was studied as a function of nitric acid, DTPA, and citric acid concentrations. The conditions needed for the mutual separation of Am(III) and Eu(III) from the loaded organic phase were optimized. Our studies revealed the possibility of separating trivalent actinides from HLLW using these completely incinerable reagents. (orig.)

  2. The liquid membrane for extraction of Yttrium and Dysprosium from Acid Nitric

    International Nuclear Information System (INIS)

    The determination of surfactant in liquid membrane has been done. The surfactant is span-80 (sorbitol-monooleate), the liquid membrane phase was the organic phase (O), the internal liquid phase (W) with ratio O/W = 1, and surfactant. The organic phase using D2EHPA in the kerosene and the internal liquid phase using aqua des or acid nitric. The determination of surfactant with variation of span-80 (0,25 - 2%) in the liquid membrane volume. The speed of stirrer was 3500 rpm in 20 minute. The ratio of liquid membrane phase form and external phase (aqua des or acid nitric) was 1, the speed of stirrer was 350 rpm in 10 minute (permeation process). The liquid phase and the liquid membrane phase was separated and then determinated the volume of liquid membrane, the result of percentage of span-80 was 0,25 % volume. The extraction of yttrium and dysprosium in 2 M HNO3 was Kdy = 2.945 and KdDy = 0.019

  3. Separation of Technetium in Nitric Acid Solution With an Extractant Impregnated Resin

    International Nuclear Information System (INIS)

    An extractant impregnated resin (EIR) was prepared by impregnation of Aliquat 336 into Amberlite XAD-4 for separation of technetium from rhodium in nitric acid solution. The prepared EIR showed high preference for rhenium (chemical analogue of technetium) over rhodium. The adsorption isotherms for rhenium were described well by Langmuir equation in both the single and multi-component systems. Maximum adsorption capacities obtained by modelling the isotherms of rhenium were 2.01 meq g-1 and 1.97 meq g-1 for the single and the multi-component systems, respectively. Column tests were also performed to confirm the separation efficiency of rhenium using a jacketed glass column (diam. 11 x L 150). The EIR column showed successful separation of rhenium with the breakthrough volume of about 122 BV for the breakthrough concentration of 0.08. Also the breakthrough data were modelled successfully by assuming a homogeneous diffusion model in the particle phase. The diffusivities obtained from the modelling were in the order of 10-7 cm2 min-1 for a rhenium. The rhenium adsorbed on the bed could be eluted with a high purity by using a nitric acid solution. (authors)

  4. Homogeneous nucleation rates of nitric acid dihydrate (NAD at simulated stratospheric conditions – Part II: Modelling

    Directory of Open Access Journals (Sweden)

    O. Möhler

    2006-01-01

    Full Text Available Activation energies ΔGact for the nucleation of nitric acid dihydrate (NAD in supercooled binary HNO3/H2O solution droplets were calculated from volume-based nucleation rate measurements using the AIDA (Aerosol, Interactions, and Dynamics in the Atmosphere aerosol chamber of Forschungszentrum Karlsruhe. The experimental conditions covered temperatures T between 192 and 197 K, NAD saturation ratios SNAD between 7 and 10, and nitric acid molar fractions of the nucleating sub-micron sized droplets between 0.26 and 0.28. Based on classical nucleation theory, a new parameterisation for ΔGact=A×(T ln SNAD−2+B is fitted to the experimental data with A=2.5×106 kcal K2 mol−1 and B=11.2−0.1(T−192 kcal mol−1. A and B were chosen to also achieve good agreement with literature data of ΔGact. The parameter A implies, for the temperature and composition range of our analysis, a mean interface tension σsl=51 cal mol−1 cm−2 between the growing NAD germ and the supercooled solution. A slight temperature dependence of the diffusion activation energy is represented by the parameter B. Investigations with a detailed microphysical process model showed that literature formulations of volume-based (Salcedo et al., 2001 and surface-based (Tabazadeh et al., 2002 nucleation rates significantly overestimate NAD formation rates when applied to the conditions of our experiments.

  5. U.S. Department of Energy radioactive nitric acid shipping campaign

    International Nuclear Information System (INIS)

    This report is about the disposal of a large quantity of chemicals previously used in the Plutonium/Uranium Extraction Plant (PUREX). Several alternatives were considered for disposal of the over 700,000 liters of this radiologically contaminated nitric acid. These alternatives included sugar denitration, biodenitrification, calcination, chemical conversion to solid sodium nitrate or to ammonium nitrate, or decontamination and re-use. Another alternative was to solicit interest from others that might be able to utilize this material in its current condition. British Nuclear Fuels Inc., located in the United Kingdom, expressed interest in this alternative. DOE Headquarters requested Westinghouse Hanford Company (WHC) Transportation and Packaging group to investigate the feasibility of transferring the radiologically contaminated nitric acid to the United Kingdom. Shipments began in May 1995, and were monitored with DOE's satellite tracking system TRANSCOM. This shipping campaign was successfully completed, with no incidents, and savings realized for cleanup of the PUREX facility in excess of $37 million. This process will be duplicated at the Savannah River Site, with cooperation between SRS and Hanford personnel sharing lessons learned

  6. A method for concentrating organic dyes: colorimetric measurements of nitric oxides and sialic acids.

    Science.gov (United States)

    Lalezari, Parviz; Lekhraj, Rukmani; Casper, Diana

    2011-09-01

    A new method for extraction and concentration of organic dyes that uses a reagent composed of a nonionic detergent mixed with an alcohol is described. We have observed that water-soluble organic dyes are also soluble in nonionic detergents and can be extracted by adding salt, which separates the dye-detergent component from the aqueous phase. We have also found that mixing nonionic detergents with alcohols markedly reduces their viscosity and produces stable, free-flowing, and effective reagents for color extraction. On the basis of these observations, we used a mixture of Triton X-100 and 1-butanol and observed that water-soluble natural and synthetic chromophores, as well as dyes generated in biochemical reactions, can be extracted, concentrated, and analyzed spectrophotometrically. Trypan blue and phenol red are used as examples of synthetic dyes, and red wine is used as an example of phenolic plant pigments. Applications for quantification of nitric oxides and sialic acids are described in more detail and show that as little as 0.15 nmol of nitric oxide and 0.20 nmol of sialic acid can be detected. A major advantage of this method is its ability to concentrate chromophores from dye-containing solutions that otherwise cannot be measured because of their low concentrations. PMID:21605540

  7. Dissolutions of oxide dispersion strengthened ferritic steels in various nitric acid solutions. Martensitic 9Cr-ODS steels

    International Nuclear Information System (INIS)

    Corrosion resistance of fuel pin cladding tube materials is one of the most important properties to design advanced aqueous reprocessing process. The martensitic oxide dispersion strengthened ferritic steel, named as '9Cr-ODS' steel, is the primary candidate material for high burnup fuel pin cladding tube in fast reactor cycle system. Because 9Cr-ODS steel contains lower chromium than stainless steels, oxidizing species such as high nitric acid concentrations and metallic ions need to reduce its corrosion rate. In nitric acid medium in contact with 9Cr-ODS steel, both nitric acid and metallic ions concentrations gradually change and stabilize protective passive layer effectively in rotary drum type continuous dissolvers. (author)

  8. Nitric acid extraction with monoamide and diamide monitored by second harmonic generation at the water/dodecane interface

    International Nuclear Information System (INIS)

    The interfacial properties of the DEHiBA and DMDBTDMA extractant molecules used in the nuclear industry are examined to obtain a better understanding of ion transfer across the water/oil interface. Optical second harmonic generation (SHG) is used in combination with bulk nitric acid titration and interfacial tension (IFT) measurements. First, the amphiphilic properties of both extractant molecules are characterized by static IFT. Second, real time SHG experiments and titration are carried out to follow the kinetics of nitric acid extraction. The SHG intensity evolution is strongly dependant on the extractant concentration in the organic phase and the SHG intensity fluctuations are correlated with the nitric acid flux across the interface. It suggests that these intensity fluctuations are the signature of a strong modification of extractant concentration at the interface that is maximal close to a critical aggregation concentration of extractant in the organic phase. (authors)

  9. Oxidation-reduction reactions of simple hydroxamic acids and plutonium(IV) ions in nitric acid

    OpenAIRE

    Carrott, M. J.; Fox, O. D.; LeGurun, G.; Jones, C J; Mason, C; Taylor, Robin; Andrieux, Fabrice; Boxall, Colin

    2008-01-01

    Simple hydroxamic acids such as formo- and aceto-hydroxamic acids have been proposed as suitable reagents for the separation of either Pu and/or Np from U in modified or single cycle Purex based solvent extraction processes designed to meet the emerging requirements of advanced fuel cycles. The stability of these hydroxamic acids is dominated by their decomposition through acid hydrolysis. Kinetic studies of the acid hydrolysis of formo- and acetohydroxamic acids are reported in the absence a...

  10. Microwave-assisted digestion procedures for biological samples with diluted nitric acid: identification of reaction products.

    Science.gov (United States)

    Gonzalez, Mário H; Souza, Gilberto B; Oliveira, Regina V; Forato, Lucimara A; Nóbrega, Joaquim A; Nogueira, Ana Rita A

    2009-07-15

    Microwave-assisted sample preparation using diluted nitric acid solutions is an alternative procedure for digesting organic samples. The efficiency of this procedure depends on the chemical properties of the samples and in this work it was evaluated by the determination of crude protein amount, fat and original carbon. Soybeans grains, bovine blood, bovine muscle and bovine viscera were digested in a cavity-microwave oven using oxidant mixtures in different acid concentrations. The digestion efficiency was evaluated based on the determination of residual carbon content and element recoveries using inductively coupled plasma optical emission spectrometry (ICP OES). In order to determine the main residual organic compounds, the digests were characterized by nuclear magnetic resonance ((1)H NMR). Subsequently, studies concerning separation of nitrobenzoic acid isomers were performed by ion pair reversed phase liquid chromatography using a C18 stationary phase, water:acetonitrile:methanol (75:20:5, v/v/v)+0.05% (v/v) TFA as mobile phase and ultraviolet detection at 254 nm. Sample preparation based on diluted acids proved to be feasible and a recommendable alternative for organic sample digestion, reducing both the reagent volumes and the variability of the residues as a result of the process of decomposition. It was shown that biological matrices containing amino acids, proteins and lipids in their composition produced nitrobenzoic acid isomers and other organic compounds after cleavage of chemical bonds. PMID:19559896

  11. Thermodynamics of uranium extraction from nitric acid solution by TBP loaded on inert supporting material

    International Nuclear Information System (INIS)

    Thermodynamic investigation of the extraction of both uranium(VI) and uranium(IV) from nitric acid solutions using tri-n-butyl phosphate (TBP) loaded on polyacrylic acid polymer (SM-7) as an inert supporting material has been done using batch technique. The effect of temperature on the equilibrium extraction values has been utilized to evaluate the change in standard thermodynamic quantities (viz. ΔH, ΔS, and ΔG). The Freundlich isotherm was successfully applied to the extraction data of both metal ions. The Dubinin-Radushkevich (D-R) isotherm was found to be valid only in case of U(IV) extraction. Based on the D-R expression, the maximum extraction capacity of loaded TBP and the mean free energy of U(IV) extraction have been determined. (author)

  12. Investigation of uranium sorption from nitric acid solutions by different ion exchange materials

    International Nuclear Information System (INIS)

    One acquired data on U sorption from the reference nitric acid solutions based on the ion-exchange resins varying in the rank. The KRF-20 phosphoric acid cationite, the ampholyte with the iminodiphosphonic groups (S-950) and the cationite with the mixed phosphonic and sulfogroups (S-957) were shown to manifest the best sorption characteristics as to U. One determined the dependences of the static exchange capacity of the above-mentioned resins on HNO3 concentration, the values of the capacity prior to breakthrough (CPB) as to U, as well as the U sorption isotherms at HNO3 concentration equal to 1 and 3 mole/l. One showed the possibility of the desorption of the absorbed U by Na2CO3 hot solutions

  13. Electrochemical oxidation of 243Am(III) in nitric acid by a terpyridyl-derivatized electrode

    Energy Technology Data Exchange (ETDEWEB)

    Dares, C. J.; Lapides, A. M.; Mincher, B. J.; Meyer, T. J.

    2015-11-05

    A high surface area, tin-doped indium oxide electrode surface-derivatized with a terpyridine ligand has been applied to the oxidation of trivalent americium to Am(V) and Am(VI) in nitric acid. Potentials as low as 1.8 V vs. the saturated calomel electrode are used, 0.7 V lower than the 2.6 V potential for one-electron oxidation of Am(III) to Am(IV) in 1 M acid. This simple electrochemical procedure provides, for the first time, a method for accessing the higher oxidation states of Am in non-complexing media for developing the coordination chemistries of Am(V) and Am(VI) and, more importantly, for separation of americium from nuclear waste streams.

  14. Radiation-chemical behaviour of Rh(3) in perchloric and nitric acid media

    International Nuclear Information System (INIS)

    Rhodium(3) behaviour in solutions of concentrated (> 1 mol/l) nitric and perchloric acids under 60Co gamma radiation with dose rate of 3.5 Gy/s has been studied. It is shown that in case of nitrate solution irradiation by doses up to 2x104 Gy, rhodium(3) concentration does not change. Rhodium(3) proved to be stable in perchlorate solutions in case of irradiation by doses up to 3x104 Gy; however, in the presence of organic acids and alcohols its reduction to methane occurred. Kinetic characteristics of rhodium(3) reduction by ethyl alcohol by the doses up to 4x104 Gy have been ascertained, reduction mechanism being considered. 6 refs.; 4 figs.; 1 tab

  15. Low Temperature Selective Catalytic Reduction of Nitrogen Oxides in Production of Nitric Acid by the Use of Liquid

    OpenAIRE

    Kabljanac, Ž.; Herjavec, I.; Mikoč, K.; Vdović, D.; Ljubičić, M.; Zečević, N.

    2011-01-01

    This paper presents the application of low-temperature selective catalytic reduction of nitrous oxides in the tail gas of the dual-pressure process of nitric acid production. The process of selective catalytic reduction is carried out using the TiO2/WO3 heterogeneous catalyst applied on a ceramic honeycomb structure with a high geometric surface area per volume. The process design parameters for nitric acid production by the dual-pressure procedure in a capacity range from 75 to 100 % in comp...

  16. Modelling of nitric acid production in the Advanced Cold Process Canister due to irradiation of moist air

    International Nuclear Information System (INIS)

    This report summarises the work performed for SKB of Sweden on the modelling of nitric acid production in the gaseous environment of the Advanced Cold Process Canister (ACPC). The model solves the simultaneous chemical rate equations describing the radiation chemistry of He/Ar/N2/O2/H2O gas mixture, involving over 200 chemical reactions. The amount of nitric acid produced as a function of time for typical ACPC conditions has been calculated using the model and the results reported. 11 refs, 11 figs, 1 tab

  17. State-of-the-art for the production of nitric acid with regard to the IPPC directive

    International Nuclear Information System (INIS)

    The aim of this study is to describe state-of-the-art technologies for nitric acid production in view of the IPPC-directive. The study gives a general survey of applied technologies, starting materials, and emissions (incl. wastes and residual materials) specific to the production of nitric acid. An essential feature of the study is to point out the potential of reduction of atmospheric pollutants. Process integrated measures and end-of-pipe technologies for the reduction of air emissions are described. Cost estimates for selected end-of-pipe technologies are given. The specific situation in Austria is described. (author)

  18. Separation of uranium from solid (U, Pu, Ag) oxide analytical waste: effect of batch size and nitric acid molarity

    International Nuclear Information System (INIS)

    Earlier we had studied the effect of leaching of a solid analytical waste of (U,Pu)O2 and AgCl with nitric acid of different molarities for identical as well as varying time intervals and the effect of leaching of this waste with nitric acid as a function of batch size (5,10, 20 g). In the present work, the effect of multistep leaching of a 25 g lot of this analytical waste with 4 and 8 M HNO3 was studied. The concentrations of U, Pu and silver were determined using ICP-AES. The results are discussed in this report. (author)

  19. The effect of nitric acid exposure on Galileo spacecraft titanium alloy Ti-6Al-4V propellant tanks

    Science.gov (United States)

    Hsieh, Cheng; O'Donnell, Tim; Yavrouian, Andre

    1990-01-01

    The Ti-6Al-4V-constructed retropropulsion-module tanks of the Galileo spacecraft were purged with nitrogen tetroxide in order to wait out a major launch rescheduling; nitric acid is among the residual products of such an operation. A test program was conducted on representative samples to ascertain the fracture toughness and stress corrosion threshold of the tanks' material, in view of Space Shuttle safety and mission-reliability requirements. It was found that the tanks' structural integrity was not degraded by nitric acid exposure.

  20. Extraction of U(VI) and Th(IV) from nitric acid solutions with N,N,N',N'-tetrahexylsuccinylamide

    International Nuclear Information System (INIS)

    A new diamide N,N,N',N'-tetrahexylsuccinylamide (THSA) was synthesized, characterised and used for the extraction of U(V) and Th(IV) from nitric acid solutions in a diluent composed of 50% 1,2,4-trimethylbenzene (TMB) and 50% kerosene (OK). Extraction distribution coefficients of U(VI) and Th(IV) as a function of aqueous nitric acid concentration, extractant concentration and temperature have been studied. The composition of extracted species, equilibrium constants and enthalpies of extraction reactions have also been calculated. The IR spectra of saturated extraction of U(VI) and Th(IV) were recorded. (author)

  1. Extraction of U(VI) and Th(IV) in nitric acid medium with N,N,N',N'-tetrahexylsuccinylamide

    International Nuclear Information System (INIS)

    The extraction mechanisms of U(VI) and Th(IV) in nitric acid solutions with N,N,N',N'-tetrahexylsuccinylamide (THSA) were described. The effects of nitric acid concentration, THSA concentration and temperature on the distribution coefficients of U(VI) and Th(IV), and the back extraction behaviours of U(VI) and Th(IV) from organic phase were studied. The compositions of the complex are found to be UO2(NO3)2·THSA and Th(NO3)4·2THSA. The equilibrium constants and thermodynamical functions of the extraction reactions have been calculated

  2. Extraction of uranium, thorium, scandium and zirconium by trioxides of tetraphenyl alkylene diphosphates from nitric acid solutions

    International Nuclear Information System (INIS)

    Some regularities of interphase distribution of microquantities of U(6), Th(4), Sc(3), Zr(4) between aqueous solutions of nitric acid and dichloroethane solutions of tetraphenyl alkylene diphosphine dioxides are studies. Effect of structure of dioxide molecule on own extraction ability and selectivity is considered. Changes of extraction ability of dioxides of alkylenediphosphines with increase of a number of methylene members in chain combining two phosphoryl groups and effect of substituent in the molecule of ethylene diphosphine dioxides on extraction of elements from nitric acid solutions are investigated. Stoichiometry of solvates extracted is determined

  3. Isolation of actinides and lanthanides by flotation from nitric acid solutions in the form of the complexes with diphosphinedioxides

    International Nuclear Information System (INIS)

    Isolation of europium, plutonium (4) and americium by ionic flotation from nitric acid solutions (1-5 mol/l HNO3), using diphosphinedioxides as surfactant-precipitator, was investigated. Increase in the metal isolation degree with an increase in flotation agent consumption was ascertained. When flotation agent is in excess, required for precipitation completeness, the metals studied are noticeably extracted from moderately concentrated solutions of nitric acid (3-3.5 mol/l), moreover, tolyl-containing diphosphinedioxide per one flotation operation extracts ∼90 % of plutonium, ∼75 % of americium and >75 % of europium

  4. Involvement of Nitric Oxide on Calcium Mobilization and Arachidonic Acid Pathway Activation during Platelet Aggregation with different aggregating agonists

    OpenAIRE

    Banerjee, Debipriya; Mazumder, Sahana; Kumar Sinha, Asru

    2016-01-01

    Platelet aggregation by different aggregating agonists is essential in the normal blood coagulation process, the excess of which caused acute coronary syndrome (ACS). In all cases, the activation of arachidonic acid by cycloxygenase was needed for the synthesis of thromboxane A2 (TXA2) but the mechanism of arachidonic acid release in platelets remains obscure. Studies were conducted to determine the role of nitric oxide (NO), if any, on the release of arachidonic acid in platelets. The cytoso...

  5. Transport of neodymium from nitric acid solution by non-dispersive solvent extraction using a hollow fiber contactor

    International Nuclear Information System (INIS)

    Transport behaviour of neodymium from nitric acid medium was investigated using hollow fiber non-dispersive extraction technique employing a mixture of di-nonyl phenyl phosphoric acid (DNPPA) and tri-n-octylphosphine oxide (TOPO) in petrofin as the solvent. The effect of feed acidity and Nd concentration was studied in counter current mode at a feed as well as organic phase flow rate of 100 mL/min. (author)

  6. DISSOLUTION OF PLUTONIUM METAL IN 8-10 M NITRIC ACID

    Energy Technology Data Exchange (ETDEWEB)

    Rudisill, T. S.; Pierce, R. A.

    2012-07-02

    The H-Canyon facility will be used to dissolve Pu metal for subsequent purification and conversion to plutonium dioxide (PuO{sub 2}) using Phase II of HB-Line. To support the new mission, the development of a Pu metal dissolution flowsheet which utilizes concentrated (8-10 M) nitric acid (HNO{sub 3}) solutions containing potassium fluoride (KF) is required. Dissolution of Pu metal in concentrated HNO{sub 3} is desired to eliminate the need to adjust the solution acidity prior to purification by anion exchange. The preferred flowsheet would use 8-10 M HNO{sub 3}, 0.015-0.07 M KF, and 0.5-1.0 g/L Gd to dissolve the Pu up to 6.75 g/L. An alternate flowsheet would use 8-10 M HNO{sub 3}, 0.05-0.2 M KF, and 1-2 g/L B to dissolve the Pu. The targeted average Pu metal dissolution rate is 20 mg/min-cm{sup 2}, which is sufficient to dissolve a “standard” 2250-g Pu metal button in 24 h. Plutonium metal dissolution rate measurements showed that if Gd is used as the nuclear poison, the optimum dissolution conditions occur in 10 M HNO{sub 3}, 0.04-0.05 M KF, and 0.5-1.0 g/L Gd at 112 to 116 °C (boiling). These conditions will result in an estimated Pu metal dissolution rate of ~11-15 mg/min-cm{sup 2} and will result in dissolution times of 36-48 h for standard buttons. The recommended minimum and maximum KF concentrations are 0.03 M and 0.07 M, respectively. The data also indicate that lower KF concentrations would yield dissolution rates for B comparable to those observed with Gd at the same HNO{sub 3} concentration and dissolution temperature. To confirm that the optimal conditions identified by the dissolution rate measurements can be used to dissolve Pu metal up to 6.75 g/L in the presence of representative concentrations of Fe and Gd or B, a series of experiments was performed to demonstrate the flowsheets. In three of the five experiments, the offgas generation rate during the dissolution was measured and samples were analyzed for hydrogen gas (H{sub 2}). The use of

  7. Ion flotation behaviour of thirty-one metal ions in mixed hydrochloric/nitric acid solutions.

    Science.gov (United States)

    Hualing, D; Zhide, H

    1989-06-01

    The ion flotation of 31 metal ions in hydrochloric/nitric acid solution with the cationic surfactant cetylpyridinium chloride was investigated. A 25-ml portion of 0.27-2.87 x 10(-4)M metal ion and 1.8-6.0 x 10(-4)M cetylpyridinium chloride solution in 0.17-3.4M acid mixture ([HCl]:[HNO(3)] = 2.4:1) was subjected to flotation in a cell, 22.5 cm high and 4.0 cm in diameter, for 5 min, with nitrogen bubbles. Ir(IV), Pt(IV), Ge(IV), Sn(IV), Bi(III), Au(III), Tl(III), Pd(II) and Sn(II) were floated from solution in 95-100% yield; Ru(III), Rh(III), Ir(III), Hg(II), Ag(I) and Tl(I) were partly floated, while Cr(VI), Ti(IV), Zr(IV), Ga(III), In(III), Fe(III), Sb(III), Al(III), Mn(II), Fe(II), Co(II), Ni(II), Cu(II), Zn(II), CD(II) and Pb(II) were floated with less than 20% yield. The flotation behaviour of these metal ions in the mixed acid system was compared with that in hydrochloric acid. The flotation is more efficient in the mixed acid system. PMID:18964771

  8. Kinetics of reduction of nitric acid by electrochemical method and validation of cell design for plant application

    International Nuclear Information System (INIS)

    Employing electrochemical method, the concentration of nitric acid had been reduced from 4 to about 0.5 M, under constant current/potential conditions in batch mode, for the purpose of optimizing the process parameters for the destruction of nitric acid in radioactive liquid waste, with good energy efficiency. Based on the rate constants determined from the batch process, a cell assembly in cylindrical configuration was designed for the electro-reduction of nitric acid in continuous mode, in radioactive environment. The steady state concentration of the acid at the outlet was compared with that concentration calculated using model equation and the agreement between the two sets of data was found to be reasonable. Cyclic voltammetric runs were recorded to understand the reduction behavior of nitric acid on platinum electrode. The results revealed the reduction of nitrate ion to be a quasi–reversible process and for the scan rate of 0.1 V s−1, values of 3.3 × 10−6 cm2 s−1 and 1.37 × 10−3 cm s−1 were computed for the diffusion coefficient and heterogeneous electron transfer rate constant, respectively

  9. Formation of nitric and organic acids by the irradiation of ground water in a spent fuel repository

    International Nuclear Information System (INIS)

    The formation of nitric acid has been reported in the literature, e g in connection with studies of glass leaching during irradiation. These experiments were carried out in order to evaluate the behaviour of glass as a matrix for highly radioactive waste. The presence of a nitrogen containing gas phase has been found to be important for the yield of the reaction. The formation of organic acids by radiolysis of carbonate solutions has been reported. The literature on the formation of organic and nitric acids have been surveyed and discussed. A conservative estimate of the formation of nitric and organic acids has been made based on dissolved nitrogen and carbonate in groundwater in a spent fuel repository. Outside a 10 cm thick copper canister containing spent fuel (the Swedish KBS-3 concept) the conservatively estimated total production of nitric, formic, and oxalic acids after 1 million years is 0.08 mol HNO 3, 0.06 mol HCOOH, and 0.04 mol (COOH) 2. For a thinner version of this canister with a wall thickness of only 1 cm, the conservatively estimated total production after 1 million years is 5 mol HNO 3, 4 mol HCOOH, and 3 mol (COOH) 2. (Author)

  10. The extraction of uranium (VI) and plutonium (IV) from nitric acid solutions with N,N-dialkyl substituting amides

    International Nuclear Information System (INIS)

    The use of N,N-di-2-methylheptyl acetamide (DMHAA),N,N-di-butylbutylamide(DBBA) and N,N-di-butylheptylamide(DBHA) as extractants for the extraction of nitric acid, U(VI) and Pu(IV) from the nitric acid solution has been investigated. The molar ratios of DBHA-HNO3 and DBHA-UO2(NO3)2 complexes are found to be 1:1 and 2:1 respectively. The complexes of both nitric acid and uranyl nitrate with these amides are highly soluble in aromatic diluent such as toluene without any formation of the third phase. The results show that, by modifying the length of the substitute chain and the degree of branch chain, some substituted amides might be found with which U(VI) and Pu(IV) could be co-extracted at moderate nitric acid solution and Pu(IV) could be preferably stripped at low acidity, and the separation of U(VI) and Pu(IV) could be accomplished without reductant of U(VI) and Pu(IV) in amide extraction

  11. Nitric oxide metabolism and indole acetic acid biosynthesis cross-talk in Azospirillum brasilense SM.

    Science.gov (United States)

    Koul, Vatsala; Tripathi, Chandrakant; Adholeya, Alok; Kochar, Mandira

    2015-04-01

    Production of nitric oxide (NO) and the presence of NO metabolism genes, nitrous oxide reductase (nosZ), nitrous oxide reductase regulator (nosR) and nitric oxide reductase (norB) were identified in the plant-associated bacterium (PAB) Azospirillum brasilense SM. NO presence was confirmed in all overexpressing strains, while improvement in the plant growth response of these strains was mediated by increased NO and indole-3-acetic acid (IAA) levels in the strains. Electron microscopy showed random distribution to biofilm, with surface colonization of pleiomorphic Azospirilla. Quantitative IAA estimation highlighted a crucial role of nosR and norBC in regulating IAA biosynthesis. The NO quencher and donor reduced/blocked IAA biosynthesis by all strains, indicating their common regulatory role in IAA biosynthesis. Tryptophan (Trp) and l-Arginine (Arg) showed higher expression of NO genes tested, while in the case of ipdC, only Trp and IAA increased expression, while Arg had no significant effect. The highest nosR expression in SMnosR in the presence of IAA and Trp, along with its 2-fold IAA level, confirmed the relationship of nosR overexpression with Trp in increasing IAA. These results indicate a strong correlation between IAA and NO in A. brasilense SM and suggest the existence of cross-talk or shared signaling mechanisms in these two growth regulators. PMID:25700632

  12. CHF enhancement in flow boiling system with TSP and boric acid solutions under atmospheric pressure

    International Nuclear Information System (INIS)

    In this study, the effects of tri-sodium phosphate (TSP) and boric acid on CHF enhancement were studied. Both TSP and boric acid are used to control pH in nuclear power plants. TSP is a kind of surfactant, and several surfactants, include TSP, have been reported to have an effect on enhancement of heat transfer. Nothing has yet been reported for the case of boric acid. CHF experiments were performed with mass flux ranging from 100-500 kg/m2 s and inlet subcooling temperature of 50 oC under atmospheric pressure. The test section was a vertical circular SS316 tube having an inner diameter of 10.98 mm. Its heated length was 224 mm, and it was heated by a heat flux control system using DC electricity. Fluids in the test loop were plain water, TSP solutions, and boric acid solutions. TSP solutions had three concentrations (0.2, 0.4, 0.6%), and boric acid solutions had four concentrations (0.2, 0.4, 0.6, 0.8%). In the case of TSP, 21.4% enhancement of CHF was observed at the inlet subcooling temperature of 50 oC and extremely low mass flux (100 kg/m2 s). In the case of boric acid, 12.4% enhancement of CHF was observed at inlet subcooling temperature of 50 oC and extremely low mass flux 100 kg/m2 s.

  13. Extraction of lanthanide(III) and uranyl(VI) from nitric acid solution by malonamides

    International Nuclear Information System (INIS)

    The extractive properties of two malonamide extractants, DMDBO3NPDA and DMDBMA were investigated for the extraction of lanthanide(III) and uranyl(VI) ions in benzene-nitric acid systems. It was found that DMDBO3NPDA has a higher extractive capacity than DMDBMA. The difference in their extracting capacities is discussed, based on the enthalpy changes for the extraction reactions and IR data for complexes of metal nitrates with malonamides. In addition, the applicability of a mixed solvent of n-dodecane and some aliphatic alcohols as a diluent for DMDBO3NPDA was examined. the longer the carbon chain and the higher the concentration of the aliphatic alcohol, the more the phase compatibility improves. The distribution ratios of neodymium(III) ion increase with an increase in the carbon chain length of linear aliphatic alcohol and with a decrease in its concentration

  14. Pb(II leaching from waste CRT funnel glass in nitric acid solutions

    Directory of Open Access Journals (Sweden)

    A. Strzałkowska

    2012-12-01

    Full Text Available Purpose: The paper presents experimental results of Pb (II leaching from waste CRT funnel glass using solution of nitric acid (V . This work focused on examining the impact of concentration and particle size on the leaching percentage of Pb (II from funnel glass.Design/methodology/approach: Material for the investigation was crushed and sieved. Leaching was carried out using working solutions pfrom co repared ncentrated HNO3 and mechanical stirrer.Findings: The received results show the possibility of find the parameters of leaching that could remove the whole Pb(II from funnel glass.Practical implications: Results after additional research can be applicate by glass industry.Originality/value: Worked out technologies can be used in glass recycling and production.

  15. Potentiality of uranium biosorption from nitric acid solutions using shrimp shells.

    Science.gov (United States)

    Ahmed, S H; El Sheikh, E M; Morsy, A M A

    2014-08-01

    Biosorption has gained important credibility during recent years because of its good performance and low cost. This work is concerned with studying the potentiality of the chitin component of the shrimp shells for uranium biosorption from nitric acid liquid solutions. The structural characteristics of the working chitin have been determined via Fourier Transform Infrared Spectroscopy (FTIR). The surface morphology was examined using Scanning Electron Microscopy (SEM). The adsorption capacity of biomass was investigated experimentally. The influence of contact time, pH, metal ion concentration, solution volume to mass ratio and temperature were evaluated and the results were fitted using adsorption isotherm models. The kinetic of uranium biosorption was also investigated as well as biosorption thermodynamic. PMID:24704766

  16. Sorption of uranium and thorium ions from nitric acid solution using HDEHP-Impregnated activated carbon

    International Nuclear Information System (INIS)

    Equilibrium measurements on the sorption of uranium and thorium ions from nitric acid solutions using di(2-ethyl hexyl) phosphoric (HDEHP) impregnated activated carbon have been done using batch technique. Experimental isotherms, Ferundlish, and Dubinin-Radushkevich (D-R) isotherm models. Of the models tested, D-R expression was found to represent the isotherms of both ions better over Th entire concentration range investigated than either Langmuir or Freundlish model. The changes in standard thermodynamic quantities (viz. Δ H, Δ S, and Δ G) were calculated and the maximum adsorption capacity of HDEHP impregnated carbon together with the mean free energy of both studied ions were determined using D-R approach

  17. Adsorption of butanol vapor on active carbons with nitric acid hydrothermal modification.

    Science.gov (United States)

    Cao, Yuhe; Wang, Keliang; Wang, Xiaomin; Gu, Zhengrong; Gibbons, William; Vu, Han

    2015-11-01

    Butanol can be produced from biomass via fermentation and used in vehicles. Unfortunately, butanol is toxic to the microbes, and this can slow fermentation rates and reduce butanol yields. Butanol can be efficiently removed from fermentation broth by gas stripping, thereby preventing its inhibitory effects. Original active carbon (AC) and AC samples modified by nitric acid hydrothermal modification were assessed for their ability to adsorb butanol vapor. The specific surface area and oxygen-containing functional groups of AC were tested before and after modification. The adsorption capacity of unmodified AC samples was the highest. Hydrothermal oxidation of AC with HNO3 increased the surface oxygen content, Brunauer-Emmett-Teller (BET) surface area, micropore, mesopore and total pore volume of AC. Although the pore structure and specific surface area were greatly improved after hydrothermal oxidization with 4M HNO3, the increased oxygen on the surface of AC decreased the dynamic adsorption capacity. PMID:26291412

  18. Spectrophotometric determination of Rare Earth Elements in aqueous nitric acid solutions for process control.

    Science.gov (United States)

    Rodionova, Oxana Ye; Tikhomirova, Tatyana I; Pomerantsev, Alexey L

    2015-04-15

    Noninvasive analytical control is of special interest for the complicated and hazardous production processes. On-line monitoring provides a unique opportunity to determine critical concentrations rapidly and without serious risks to operating personnel and the environment. Models for quantitative determination of concentrations of Rare Earth Elements in complex mixtures in nitric acid serve for these purposes. Here, the feasibility of simultaneous determination of cerium, praseodymium, and neodymium using the whole UV-vis spectroscopic range, together with chemometric data processing, is studied. The predictability of two chemometric techniques, partial least squares regression and correlation constrained multivariate curve resolution-alternating least squares are compared. Models' performances are analyzed in out-of-control cases. PMID:25818140

  19. Modelling of uranyl nitrate and nitric acid extraction in diluted TBP using Chem-Unifac

    International Nuclear Information System (INIS)

    Chem-UNIFAC model is applied to TBP/dodecane/water/UO2(NO3)2 and TBP/dodecane/water/HNO3 systems, following our previous studies on TBP/diluent (alkane, HCCl3, CCl4) and TBP/diluent/water/salting out agent (same diluents) systems. New Chem-UNIFAC parameters for TBP/water pair are calculated and an unique set of parameters is proposed to describe the TBP/dodecane/water/UO2(NO3)2 system, for a wide range of TBP/diluent volume proportions (10%, 30%, 50%, 100%) and a wide range of uranyl nitrate aqueous concentration. Nitric acid and water extraction in TBP/dodecane/water/HNO3 is also calculated and an improvement is found in the description of the corresponding isotherms. (authors)

  20. Studies of dissolution solutions of ruthenium metal, oxide and mixed compounds in nitric acid

    Energy Technology Data Exchange (ETDEWEB)

    Mousset, F.; Eysseric, C.; Bedioui, F

    2004-07-01

    Ruthenium is one of the fission products generated by irradiated nuclear fuel. It is present throughout all the steps of nuclear fuel reprocessing-particularly during extraction-and requires special attention due to its complex chemistry and high {beta}{gamma} activity. An innovative electro-volatilization process is now being developed to take advantage of the volatility of RuO{sub 4} in order to eliminate it at the head end of the Purex process and thus reduce the number of extraction cycles. Although the process operates successfully with synthetic nitrato-RuNO{sup 3+} solutions, difficulties have been encountered in extrapolating it to real-like dissolution solutions. In order to better approximate the chemical forms of ruthenium found in fuel dissolution solutions, kinetic and speciation studies on dissolved species were undertaken with RuO{sub 2},xH{sub 2}O and Ru{sup 0} in nitric acid media. (authors)

  1. Study on Purification Diatomite with nitric acid by Thermal Closed System

    Directory of Open Access Journals (Sweden)

    Kuang Meng

    2016-01-01

    Full Text Available In this research, a purification approach using nitric acid leaching at thermal closed system was developed to improve the porous structure of raw diatomite by removal of impurities from its surface and clogged pores. The feasibility and efficiency of this approach were determined by XRF for chemical constitution of diatomite, SEM for morphology and BET for specific surface area of purified diatomite. The investigations indicated that the content of SiO2 was in order of 85.14% for raw diatomite and 98% for purified diatomite, the content of Fe2O3 decreases after purified; the integrity of the porous structure was confirmed by SEM, and increase in specific surface area from 18m2·g-1 to 36m2·g-1.

  2. Vapor pressures of solid hydrates of nitric acid - Implications for polar stratospheric clouds

    Science.gov (United States)

    Worsnop, Douglas R.; Fox, Lewis E.; Zahniser, Mark S.; Wofsy, Steven C.

    1993-01-01

    Thermodynamic data are presented for hydrates of nitric acid: HNO3.H2O, HNO3.2H2O, HNO3.3H2O, and a higher hydrate. Laboratory data indicate that nucleation and persistence of metastable HNO3.2H2O may be favored in polar stratospheric clouds over the slightly more stable HNO3.3H2O. Atmospheric observations indicate that some polar stratospheric clouds may be composed of HNO3.2H2O and HNO3.3H2O. Vapor transfer from HNO3.2H2O to HNO3.3H2O could be a key step in the sedimentation of HNO3, which plays an important role in the depletion of polar ozone.

  3. Vapor pressures of solid hydrates of nitric Acid: implications for polar stratospheric clouds.

    Science.gov (United States)

    Worsnop, D R; Zahniser, M S; Fox, L E; Wofsy, S C

    1993-01-01

    Thermodynamic data are presented for hydrates of nitric acid: HNO(3).H(2)O, HNO(3).2H(2)O, HNO(3).3H(2)O, and a higher hydrate. Laboratory data indicate that nucleation and persistence of metastable HNO(3).2H(2)O may be favored in polar stratospheric clouds over the slightly more stable HNO(3).3H(2)O. Atmospheric observations indicate that some polar stratospheric clouds may be composed of HNO(3).2H(2)O and HNO(3).3H(2)O. Vapor transfer from HNO(3).2H(2)O to HNO(3).3H(2)O could be a key step in the sedimentation of HNO(3), which plays an important role in the depletion of polar ozone. PMID:17757475

  4. Recovery of Lead from Sulfide Concentrate after Mechanochemical Activation Using Nitric Acid

    Institute of Scientific and Technical Information of China (English)

    A.G.Kholmogorov; O.N.Kononova; G.L.Pashkov; L.V.Shashina; V.P.Plekhanov; A.A.Sabetskiy

    2005-01-01

    Decomposition of lead sulfide concentrates in nitric acidic solutions after ferric (Ⅲ) nitrate addition and mechanical preparation has been investigated. It was found out that the decomposition can be achieved in HNO3 solution (>1.5 mol·L-1) at the temperature above 85℃. The leaching rate of lead can be increased by means of mechanochemical activation. The use of [Fe(NO3)3-HNO3-H2O] aqueous salt system allows the decomposition of lead sulfide concentrate at room temperature and in this case the concentration of HNO3 does not exceed 0.05-0.1 mol.L-1, The degree of lead recovery into solution from PbS concentrate reaches 99.3%-99.6c70 with the mechanochemical activation of this concentrate. The insoluble residues after the leaching contain SiO2, S0, FeCO3 and PbSO4.

  5. Supercritical fluid extraction of uranium from nitric acid medium and tissue paper matrix

    International Nuclear Information System (INIS)

    Supercritical fluid extraction (SFE) is a novel technique for metal ion extraction, which offers a promising alternate to the conventional extraction process. The technique has advantage of minimization of radioactive liquid waste. In the present study, supercritical CO2 containing small amount of TBP/TOPO as co-solvent were employed for uranium extraction. Uranium extraction efficiency of ∼ 98% was achievable from nitric acid medium employing TBP as co-solvent. However, uranium could be extracted to nearly same extent with lesser amount (1 ml) of TOPO. In SFE of uranium from tissue paper matrix extraction efficiency of 70% was obtained with TBP as co-solvent. Whereas nearly complete uranium extraction (∼99%) was achievable from tissue paper with TOPO as co-solvent. (author)

  6. Influence of different diluents on thorium extraction and third-phase formation from nitric acid medium

    International Nuclear Information System (INIS)

    Advanced heavy water reactor (AHWR) is being developed in India for the utilization of vast resources of thorium for power generation. The reprocessing of the irradiated AHWR fuel is quite challenging in view of the presence of Th, U and Pu along with fission products in the feed solution. This paper compares thorium extraction/third-phase formation behavior of TBP and DHOA dissolved in different diluents viz. n-dodecane, normal paraffinic hydrocarbon (NPH), Shelsol D 70 (SS D 70, 40 % aromatic), and Solvsso 100 (∼ 95-100 % aromatic) as a function of nitric acid concentration. The work compares the performance of SS D 70 and Solvsso 100 having aromatic components vis-à-vis n-dodecane and NPH towards Th(IV) extraction/third-phase using TBP and DHOA as extractants. It is observed that presence of aromatic component in the diluent helps in increasing the Th(IV)-LOC value

  7. Studies of dissolution solutions of ruthenium metal, oxide and mixed compounds in nitric acid

    International Nuclear Information System (INIS)

    Ruthenium is one of the fission products generated by irradiated nuclear fuel. It is present throughout all the steps of nuclear fuel reprocessing-particularly during extraction-and requires special attention due to its complex chemistry and high βγ activity. An innovative electro-volatilization process is now being developed to take advantage of the volatility of RuO4 in order to eliminate it at the head end of the Purex process and thus reduce the number of extraction cycles. Although the process operates successfully with synthetic nitrato-RuNO3+ solutions, difficulties have been encountered in extrapolating it to real-like dissolution solutions. In order to better approximate the chemical forms of ruthenium found in fuel dissolution solutions, kinetic and speciation studies on dissolved species were undertaken with RuO2,xH2O and Ru0 in nitric acid media. (authors)

  8. Sorption of Pu(IV) from nitric acid by bifunctional anion-exchange resins

    International Nuclear Information System (INIS)

    Anion exchange is attractive for separating plutonium because the Pu(IV) nitrate complex is very strongly sorbed and few other metal ions form competing anionic nitrate complexes. The major disadvantage of this process has been the unusually slow rate at which the Pu(IV) nitrate complex is sorbed by the resin. The paper summarizes the concept of bifunctional anion-exchange resins, proposed mechanism for Pu(IV) sorption, synthesis of the alkylating agent, calculation of Kd values from Pu(IV) sorption results, and conclusions from the study of Pu(IV) sorption from 7M nitric acid by macroporous anion-exchange resins including level of crosslinking, level of alkylation, length of spacer, and bifunctional vs. monofunctional anion-exchange resins

  9. Simultaneous extraction of U and Zr using HDEHP impregnated XAD-7 resin in nitric acid medium

    International Nuclear Information System (INIS)

    Feasibility of separating U and Zr from U-Zr alloys using HDEHP impregnated XAD-7 resin was explored in the present study with a view to obtain a sample solution free from matrix elements suitable for carrying out ICP-MS analysis of lanthanides at trace concentrations. Initially, the distributions of U, Zr and lanthanides in the impregnated resin were investigated with different nitric acid concentrations. The separated fractions were analyzed by ICP-MS for trace lanthanides whereas ion chromatography was employed for quantifying U and Zr. It was observed that at 4M HNO3 medium U exhibited high distribution whereas lanthanides showed least distribution in the resin. Zirconium showed significant distribution in 4M HNO3. Hence, 4M HNO3 was found to be optimal in order to extract U and Zr simultaneously. However, heavy rare earths such as Tm, Yb and Lu showed significant Kd values leading to their poor recovery. (author)

  10. Catalytic decomposition of nitrous oxide from nitric acid production tail gases. Investigation of inhibition effects. Executive summary

    International Nuclear Information System (INIS)

    Nitric acid production is an important source of nitrous oxide, one of the green-house gases. Catalytic decomposition of N2O in nitric acid tail-gases might be a possibility for emission reduction, but technology is not yet available. As a part of development of suitable catalytic systems, research was performed, aiming at: gaining an improved understanding of catalytic decomposition of N2O and the inhibiting effects of NO, NO2, H2O and O2; and preparing a 'go-no go' decision whether or not to proceed with subsequent re-search and development and if yes, to indicate what technology further development should aim for. Due to the presence of NOx and water in the nitric acid tail gases, catalytic decomposition proves not to be feasible at temperatures below 350C. At higher temperatures possibilities do exist and a number of promising catalysts are identified. These are active (80 - 100 % conversion) in the temperature range of 400 - 500C and under simulated tail gas conditions. Considering process conditions only (temperatures and composition of the tail-gases), the catalysts studied (pref. the Rh/Al2O3 types) could be in principle applied successfully in all Dutch nitric acid plants

  11. Overexpression of cationic amino acid transporter-1 increases nitric oxide production in hypoxic human pulmonary microvascular endothelial cells

    OpenAIRE

    Cui, Hongmei; Chen, Bernadette; Chicoine, Louis G.; Nelin, Leif D.

    2011-01-01

    1. The endogenous production of and/or the bioavailability of nitric oxide (NO) is decreased in pulmonary hypertensive diseases. L-arginine (L-arg) is the substrate for NO synthase (NOS). L-arg is transported into cells via the cationic amino acid transporters (CAT), of which there are two isoforms in endothelial cells, CAT-1 and CAT-2.

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

    CERN Document Server

    Melott, Ben Neuenswander Adrian

    2014-01-01

    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.

  13. PKCa Agonists Enhance the Protective Effect of Hyaluronic Acid on Nitric Oxide-Induced Apoptosis of Articular Chondrocytes in Vitro

    Directory of Open Access Journals (Sweden)

    Jian-lin Zhou

    2013-12-01

    The results may be showed that PKCa regulate the expresion of caspase-3, which contribute to the apoptosis of chondrocytes induced by NO. PKC α agonists enhance the protective effect of hyaluronic acid on nitric oxide-induced articular chondrocytes apoptosis.

  14. Ammonium nitrate evaporation and nitric acid condensation in DMT CCN counters

    Science.gov (United States)

    Romakkaniemi, S.; Jaatinen, A.; Laaksonen, A.; Nenes, A.; Raatikainen, T.

    2014-05-01

    The effect of inorganic semivolatile aerosol compounds on the cloud condensation nucleus (CCN) activity of aerosol particles was studied by using a computational model for a DMT-CCN counter, a cloud parcel model for condensation kinetics and experiments to quantify the modelled results. Concentrations of water vapour and semivolatiles as well as aerosol trajectories in the CCN column were calculated by a computational fluid dynamics model. These trajectories and vapour concentrations were then used as an input for the cloud parcel model to simulate mass transfer kinetics of water and semivolatiles between aerosol particles and the gas phase. Two different questions were studied: (1) how big a fraction of semivolatiles is evaporated from particles after entering but before particle activation in the DMT-CCN counter? (2) How much can the CCN activity be increased due to condensation of semivolatiles prior to the maximum water supersaturation in the case of high semivolatile concentration in the gas phase? Both experimental and modelling results show that the evaporation of ammonia and nitric acid from ammonium nitrate particles causes a 10 to 15 nm decrease to the critical particle size in supersaturations between 0.1% and 0.7%. On the other hand, the modelling results also show that condensation of nitric acid or similar vapour can increase the CCN activity of nonvolatile aerosol particles, but a very high gas phase concentration (as compared to typical ambient conditions) would be needed. Overall, it is more likely that the CCN activity of semivolatile aerosol is underestimated than overestimated in the measurements conducted in ambient conditions.

  15. Investigation on surface structure of potassium permanganate/nitric acid treated poly(tetrafluoroethylene)

    International Nuclear Information System (INIS)

    Highlights: • A new transformation (conversion) mechanism of PTFE surface from a hydrophobicity to a hydrophilicity was proposed through the treatment of KMnO4/HNO3. • Chemical reactions or defluorination of PTFE described in the reported paper was testified to be a misconceived conclusion by the combination of several testing measurements (IR, XPS, XRD and so on) in our present work. • Deposition of manganese oxide and/or manganese hydroxide on PTFE surface contributed to the hydrophilic property of the modified PTFE with KMnO4/HNO3 treated. • The deposition thickness on the modified PTFE surface was about 5 μm, which was significantly helpful in enhancing the adhesive strength of PTFE with other materials. - Abstract: In the previous articles concerning the treatment of poly(tetrafluoroethylene) (PTFE) with potassium permanganate/nitric acid mixture, the conversion of a hydrophobic to a hydrophilic surface was partially assigned to the defluorination of PTFE and then the introduction of carbonyl and hydroxyl groups into the defluorinated sites. In the present work, PTFE sheets were treated with potassium permanganate/nitric acid, and the surfaces before and after treatment were comparatively characterized by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The surface sediments of the treated PTFE were also determined by atomic absorption spectroscopy (AAS). The results indicate that the conversion of the hydrophobicity to the hydrophilicity on the modified PTFE surface is mainly due to the deposition of hydrophilic manganese oxides which covered the fluorocarbon surface, and no detectable chemical reactions of PTFE occur in the treating process

  16. Investigation on surface structure of potassium permanganate/nitric acid treated poly(tetrafluoroethylene)

    Energy Technology Data Exchange (ETDEWEB)

    Fu, Congli; Liu, Shuling; Gong, Tianlong; Gu, Aiqun; Yu, Zili, E-mail: ziliyu@scu.edu.cn

    2014-10-30

    Highlights: • A new transformation (conversion) mechanism of PTFE surface from a hydrophobicity to a hydrophilicity was proposed through the treatment of KMnO{sub 4}/HNO{sub 3}. • Chemical reactions or defluorination of PTFE described in the reported paper was testified to be a misconceived conclusion by the combination of several testing measurements (IR, XPS, XRD and so on) in our present work. • Deposition of manganese oxide and/or manganese hydroxide on PTFE surface contributed to the hydrophilic property of the modified PTFE with KMnO{sub 4}/HNO{sub 3} treated. • The deposition thickness on the modified PTFE surface was about 5 μm, which was significantly helpful in enhancing the adhesive strength of PTFE with other materials. - Abstract: In the previous articles concerning the treatment of poly(tetrafluoroethylene) (PTFE) with potassium permanganate/nitric acid mixture, the conversion of a hydrophobic to a hydrophilic surface was partially assigned to the defluorination of PTFE and then the introduction of carbonyl and hydroxyl groups into the defluorinated sites. In the present work, PTFE sheets were treated with potassium permanganate/nitric acid, and the surfaces before and after treatment were comparatively characterized by Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The surface sediments of the treated PTFE were also determined by atomic absorption spectroscopy (AAS). The results indicate that the conversion of the hydrophobicity to the hydrophilicity on the modified PTFE surface is mainly due to the deposition of hydrophilic manganese oxides which covered the fluorocarbon surface, and no detectable chemical reactions of PTFE occur in the treating process.

  17. Optimization of the nitrous vapors experimental conditions production by nitric acid electrochemical reduction; Optimisation des conditions operatoires de production de vapeurs nitreuses par reduction electrochimique d`acide nitrique

    Energy Technology Data Exchange (ETDEWEB)

    Lemaire, M.

    1996-11-22

    Gaseous nitrogen oxides (NO and NO{sub 2}) involved as oxidizing agents in nuclear fuel reprocessing can be produced by electrochemical reduction of nitric acid. This is an interesting alternative to the existing process because no wastes are generated. voltammetric studies on a platinum electrode show that two reduction potential regions are observed in concentrated nitric acid solutions, between 0,05 V{sub SHE} and between 0,5 V{sub SHE} and 1 V{sub SHE}. The highest potential region reduction mechanism was studied by: classical micro-electrolysis methods, macro-electrolysis methods, infrared spectroscopy coupled to electrochemistry. It was determined that the origin of nitric acid reduction is the electrochemical reduction of nitrous acid in nitric oxide which chemically reduces nitric acid. This reaction produces nitrous acid back which indicate an auto-catalytic behaviour of nitric acid reduction mechanism. Nitrogen dioxide evolution during nitric reduction can also explained by an other chemical reaction. If the potential value of platinum electrode is above 0,8 V{sub SHE}, products of the indirect nitric acid reduction are nitrous acid, nitrogen oxide and nitrogen dioxide. Below this value nitric oxide can be reduced in nitrous oxide. Thus the potential value is the most important parameter for the nitrogen oxides production selectivity. However, owing to the auto-catalytic character of the reduction mechanism, potential value can be controlled during intentiostatic industrial electrolysis. (author). 91 refs.

  18. Synergistic hypergolic ignition of blends of dienes and dienophiles with red fuming nitric acid as oxidizer

    Energy Technology Data Exchange (ETDEWEB)

    Panda, S.P.; Kulkarni, S.G.; Prabhakaran, C.

    1989-04-01

    Synergistic hypergolic ignition of several fuel blends and mixtures with red fuming nitric acid (RFNA) as oxidizer has been reported previously. The liquid fuels consisted of blends of 3-carene, cyclopentadiene, or norbornadiene with cardanol in the weight ratio 70:30 for the first two and 85:15 for norbornadiene. In all these cases, synergism in ignition was believed to be due to the fast and exothermic oligomerization of 3-carene, cyclopentadiene, and norbornadiene in the presence of acid. The exothermicity of the systems was enhanced by the addition of cardanol to the unsaturation of oligomers, leading to the formation of highly oxidizable phenolic ethers. Two more important reactions at the preignition stage were nitration and oxidation of the ethers leading to the production of gaseous combustibles and heat. In this case, an attempt has been made to extend the range of possible preignition reactions by introducing diene-dienophile Diels-Alder cycloaddition with low activation energy by replacing cardanol with furfuryl alcohol or furfurylideneacetone having a furan ring to behave as acid polymerizable dienes in the above systems.

  19. Hydrogen generation in SRAT with nitric acid and late washing flowsheets

    International Nuclear Information System (INIS)

    Melter feed preparation processes, incorporating a final wash of the precipitate slurry feed to Defense Waste Processing Facility (DWPF) and a partial substitution of the SRAT formic acid requirement with nitric acid, should not produce peak hydrogen generation rates during Cold Chemical Runs (CCR's) and radioactive operation greater than their current, respective hydrogen design bases of 0.024 lb/hr and 1.5 lb/hr. A single SRAT bench-scale process simulation for CCR-s produced a DWPF equivalent peak hydrogen generation rate of 0.004 lb/hr. During radioactive operation, the peak hydrogen generation rate will be dependent on the extent DWPF deviates from the nominal precipitate hydrolysis and melter feed preparation process operating parameters. Two actual radioactive sludges were treated according to the new flowsheets. The peak hydrogen evolution rates were equivalent to 0.038 and 0.20 lb/hr (DWPF scale) respectively. Compared to the formic acid -- HAN hydrolysis flowsheets, these peak rates were reduced by a factor of 2.5 and 3.4 for Tank 15 and Tank 11 sludges, respectively

  20. Integrating nitric oxide into salicylic acid and jasmonic acid/ethylene plant defense pathways

    DEFF Research Database (Denmark)

    Mur, Luis A J; Prats, Elena; Pierre, Sandra;

    2013-01-01

    Plant defence against pests and pathogens is known to be conferred by either salicylic acid (SA) or jasmonic acid (JA)/ethylene (ET) pathways, depending on infection or herbivore-grazing strategy. It is well attested that SA and JA/ET pathways are mutually antagonistic allowing defence responses...

  1. Application of Primary Abatement Technology for Reduction of N2O Emmision in Petrokemija Nitric Acid Production

    Directory of Open Access Journals (Sweden)

    Ćosić, L.

    2013-01-01

    Full Text Available Industrial nitric acid production by oxidation of gaseous ammonia with Ostwald procedure produces an unwanted by-product – colorless nitrous oxide, N2O. As emission of N2O represents a very serious problem due of its huge contribution to global warming, certain measures focused on its maximum reduction should be undertaken. Minimization of N2O emission in nitric acid production can be achieved in different parts of the process flow, depending on the applied available technologies. For the abatement of N2O emissions in Petrokemija's nitric acid production processes from the list of the best available technologies chosen were primary and secondary abatement technologies. The mentioned ensures reduction of N2O by use of improved selective heterogeneous catalysts in the step of gaseous ammonia oxidation. Precious metals in the shape of gauzes are used as selective heterogeneous catalyst in primary technology, while in the case of secondary technology the Fe2 O3 catalyst on Al2O3 support in the shape of spherical pellets is chosen. Shown is the application of primary technology for the abatement of N2O in both nitric acid production facilities and their comparison with classical heterogeneous catalyst and preparation for the installation of secondary selective catalyst. N2O emissions with the application of primary technology in both production facilities were reduced from 12 kg of N2O to 7 kg of N2O per ton of pure HNO3. With the primary reduction in N2O emissions the foundation was established for further reduction with the secondary technology to the final value of 0.7 kg of N2O per ton of pure HNO3, which represents mass concentration in the tail gas below 200 mg m-3 (at n. c.. With the applied technologies for the abatement of N2O emissions in Petrokemija's nitric acid production the future prescribed emission limit value will be satisfied.

  2. N,N-dialkyl-2-hydroxyacetamides for modifier-free separation of trivalent actinides from nitric acid medium

    Energy Technology Data Exchange (ETDEWEB)

    Prathibha, T.; Kumaresan, R.; Selvan, B. Robert; Venkatesan, K.A.; Antony, M.P.; Vasudeva Rao, P.R. [Indira Gandhi Centre for Atomic Research, Kalpakkam (India). Fuel Chemistry Div.

    2016-07-01

    The alkyl derivatives of N,N,-dialkyl-2-hydroxyacetamide (DAHyA), namely, N,N,-dihexyl-2-hydroxyacetamide (DHHyA), N,N,-dioctyl-2-hydroxyacetamide (DOHyA), N,N,-didecyl-2-hydroxyacetamide (DDHyA), were synthesized and characterized by FT-IR, and NMR spectroscopy. The extraction behaviour of Am(III) in a solution of DAHyA in n-dodecane was studied as a function of various parameters to evaluate the feasibility of using DAHyA for partitioning of trivalent actinides from high-level liquid waste (HLLW). The distribution ratio of Am(III) (D{sub Am(III)}) in 0.1 M DAHyA/n-DD increased from 10{sup -4} to > 200 with increase in nitric acid concentration from 1 M to 6 M. A D{sub Am(III)} value 10-70 was obtained in a nitric acid concentration range from 3-4 M. The extraction of Am(III) in 0.1 M DAHyA/n-dodecane decreased in the order DHHyA > DOHyA > DDHyA. The third-phase formation behaviour of nitric acid and neodymium (III) in 0.2 M DAHyA/n-dodecane was studied. Near stoichiometric amount of neodymium (III) can be loaded in octyl and decyl derivatives without any third-phase formation from 3-4 M nitric acid medium. Unlike other extractants, the loaded trivalent metal ion in DAHyA can be recovered even with 1 M nitric acid. Therefore, the study revealed that N,N,-dialkyl-2-hydroxyacetamides are promising candidates for partitioning the trivalent actinides from HLLW.

  3. Fatty acid-binding protein 4 impairs the insulin-dependent nitric oxide pathway in vascular endothelial cells

    OpenAIRE

    Aragonès Gemma; Saavedra Paula; Heras Mercedes; Cabré Anna; Girona Josefa; Masana Lluís

    2012-01-01

    Abstract Background Recent studies have shown that fatty acid-binding protein 4 (FABP4) plasma levels are associated with impaired endothelial function in type 2 diabetes (T2D). In this work, we analysed the effect of FABP4 on the insulin-mediated nitric oxide (NO) production by endothelial cells in vitro. Methods In human umbilical vascular endothelial cells (HUVECs), we measured the effects of FABP4 on the insulin-mediated endothelial nitric oxide synthase (eNOS) expression and activation a...

  4. Estimation of salivary nitric oxide and uric acid levels in oral squamous cell carcinoma and healthy controls

    OpenAIRE

    Varsha Salian; Farah Demeri; Suchetha Kumari

    2015-01-01

    Background: Oral squamous cell carcinoma (OSCC) being the most common head and neck cancer, involves the interplay of several free radicals and antioxidant molecules. The potential role of salivary nitric oxide (NO) and uric acid in cancer development needs to be explored as there are a few studies highlighting their association with each other and with oral cancer. Aims: The present study was designed to measure the NO and uric acid levels in the saliva of patients with OSCC as compared with...

  5. Validation Testing of the Nitric Acid Dissolution Step Within the K Basin Sludge Pretreatment Process

    Energy Technology Data Exchange (ETDEWEB)

    AJ Schmidt; CH Delegard; KL Silvers; PR Bredt; CD Carlson; EW Hoppe; JC Hayes; DE Rinehart; SR Gano; BM Thornton

    1999-03-24

    The work described in this report involved comprehensive bench-scale testing of nitric acid (HNO{sub 3}) dissolution of actual sludge materials from the Hanford K East (KE) Basin to confirm the baseline chemical pretreatment process. In addition, process monitoring and material balance information was collected to support the development and refinement of process flow diagrams. The testing was performed by Pacific Northwest National Laboratory (PNNL)for the US Department of Energy's Office of Spent Fuel Stabilization (EM-67) and Numatec Hanford Corporation (NHC) to assist in the development of the K Basin Sludge Pretreatment Process. The baseline chemical pretreatment process for K Basin sludge is nitric acid dissolution of all particulate material passing a 1/4-in. screen. The acid-insoluble fraction (residual solids) will be stabilized (possibly by chemical leaching/rinsing and grouting), packaged, and transferred to the Hanford Environmental Restoration Disposal Facility (ERDF). The liquid fraction is to be diluted with depleted uranium for uranium criticality safety and iron nitrate for plutonium criticality safety, and neutralized with sodium hydroxide. The liquid fraction and associated precipitates are to be stored in the Hanford Tank Waste Remediation Systems (TWRS) pending vitrification. It is expected that most of the polychlorinated biphenyls (PCBs), associated with some K Basin sludges, will remain with the residual solids for ultimate disposal to ERDF. Filtration and precipitation during the neutralization step will further remove trace quantities of PCBs within the liquid fraction. The purpose of the work discussed in this report was to examine the dissolution behavior of actual KE Basin sludge materials at baseline flowsheet conditions and validate the.dissolution process step through bench-scale testing. The progress of the dissolution was evaluated by measuring the solution electrical conductivity and concentrations of key species in the

  6. Validation Testing of the Nitric Acid Dissolution Step Within the K Basin Sludge Pretreatment Process

    International Nuclear Information System (INIS)

    The work described in this report involved comprehensive bench-scale testing of nitric acid (HNO3) dissolution of actual sludge materials from the Hanford K East (KE) Basin to confirm the baseline chemical pretreatment process. In addition, process monitoring and material balance information was collected to support the development and refinement of process flow diagrams. The testing was performed by Pacific Northwest National Laboratory (PNNL)for the US Department of Energy's Office of Spent Fuel Stabilization (EM-67) and Numatec Hanford Corporation (NHC) to assist in the development of the K Basin Sludge Pretreatment Process. The baseline chemical pretreatment process for K Basin sludge is nitric acid dissolution of all particulate material passing a 1/4-in. screen. The acid-insoluble fraction (residual solids) will be stabilized (possibly by chemical leaching/rinsing and grouting), packaged, and transferred to the Hanford Environmental Restoration Disposal Facility (ERDF). The liquid fraction is to be diluted with depleted uranium for uranium criticality safety and iron nitrate for plutonium criticality safety, and neutralized with sodium hydroxide. The liquid fraction and associated precipitates are to be stored in the Hanford Tank Waste Remediation Systems (TWRS) pending vitrification. It is expected that most of the polychlorinated biphenyls (PCBs), associated with some K Basin sludges, will remain with the residual solids for ultimate disposal to ERDF. Filtration and precipitation during the neutralization step will further remove trace quantities of PCBs within the liquid fraction. The purpose of the work discussed in this report was to examine the dissolution behavior of actual KE Basin sludge materials at baseline flowsheet conditions and validate the.dissolution process step through bench-scale testing. The progress of the dissolution was evaluated by measuring the solution electrical conductivity and concentrations of key species in the dissolver

  7. Processing of LEU targets for 99Mo production -- Dissolution of metal foils by nitric-acid/sulfuric-acid mixtures

    International Nuclear Information System (INIS)

    The first step in processing low-enriched uranium (LEU) targets for production of 99Mo is to dissolve the neutron-irradiated uranium foil coming from the reactor. Appropriate conditions for dissolving the foils were determined by measuring the dissolution rates for uranium foil over a wide range of temperatures and acid concentrations. On the basis of these dissolution rates, the process chemistry, and a model that integrates dissolution rates as a function of temperature and composition, a closed stainless-steel dissolver was designed, built, and tested for dissolving up to 18 g of uranium foil. The results were quite successful, with the uranium foil being dissolved within one hour as desired. To do this, the dissolver temperature must be in the range from 97 to 102 C, and the dissolver solution (cocktail) must have a composition of 3M nitric acid and 2M sulfuric acid. The final dissolver solution is subsequently processed to separate 99Mo from uranium, fission products, and other elements

  8. Processing of LEU targets for 99Mo production - Dissolution of metal foils by nitric-acid/sulfuric-acid mixtures

    International Nuclear Information System (INIS)

    The first step in processing low-enriched uranium (LEU) targets for production of 99Mo is to dissolve the neutron-irradiated uranium foil coming from the reactor. Appropriate conditions for dissolving the foils were determined by measuring the dissolution rates for uranium foil over a wide range of temperatures and acid concentrations. On the basis of these dissolution rates, the process chemistry, and a model that integrates dissolution rates as a function of temperature and composition, a closed stainless-steel dissolver was designed, built, and tested for dissolving up to 18 g of uranium foil. The results were quite successful, with the uranium foil being dissolved within one hour as desired. To do this, the dissolver temperature must be in the range from 97 to 102 deg. C, and the dissolver solution (cocktail) must have a composition of 3M nitric acid and ZM sulfuric acid. The final dissolver solution is subsequently processed to separate 99Mo from uranium, fission products, and other elements. (author)

  9. Determination of Nitric Acid in Aqueous Solution of Uranium and Plutonium Purification Cycle by Near Infrared Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    LI; Ding-ming; WANG; Lin; ZHANG; Li-hua; GONG; Yan-ping; MU; Ling; WU; Ji-zong

    2012-01-01

    <正>The concentration of nitric acid interfered with the distribution of uranium and plutonium in nuclear fuel reprocessing process. So, in the reprocessing process control analysis, the determination of the free acid plays an important role. Traditional laboratory analytical method of free acid needs large size sample and is time-consuming. Hence, development of fast analytical method for free acid has important significance for the reprocessing process control analysis. Near-infrared spectroscopy (NIRS) has been proved to be a powerful analytical tool and used in various fields, it’s seldom, however, used in spent

  10. Тhe impact of starter culture on the pH and the content of lactic and volatile fatty acids in boiled-smoked sausages

    OpenAIRE

    Indzhelieva, Dijana; Valkova-Jorgova, Katja; Kuzelov, Aco; Andronikov, Darko

    2015-01-01

    This paper reviews the effects of starter cultures with lactic acid bacteria as a factor of increasing quality and intensifi cation of production processes in durable boiled – smoked sausages, type of Burgas. In this regard, the impact of starter cultures in the fi lling, their role in changing the pH value, the content of lactic acid and volatile fatty acids were tested. The two types of starter were used: pure cultures Bifi dobacterium longum (B2), and mixed cultures Bifi dobacteri...

  11. Material compatibility evaluataion for DWPF nitric-glycolic acid - literature review

    International Nuclear Information System (INIS)

    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 deg 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 deg C); For 690, G30, Allcorr, Ultimet and Stellite alloys no data were available; and, 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

  12. The bonding of heavy metals on nitric acid-etched coal fly ashes functionalized with 2-mercaptoethanol or thioglycolic acid

    International Nuclear Information System (INIS)

    Coal fly ash is a waste by-product of the coal fire industry, which generates many environmental problems. Alternative uses of this material would provide efficient solutions for this by-product. In this work, nitric acid-etched coal fly ash labelled with 2-mercaptoethanol or thioglycolic acid was assessed for retention of Al(III), As(III), Cu(II), Cd(II), Fe(III), Mn(II), Hg(II), Ni(II), Pb(II) and Zn(II) ions. The bonding characteristics between the organic compounds with the solid support, as well as with the metal ions, were evaluated using various surface analytical techniques. Visualization of the organically-functionalized coal fly ash particle was possible using scanning electron microscopy (SEM), while the elemental composition of the functionalized material, before and after retention of the metal ions, was obtained by energy dispersive (ED)-X ray spectrometry (XRS) and electrothermal atomic absorption spectrometry (ETAAS). Fourier transform infrared (FT-IR) spectrometry and Raman spectrometry were used to obtain information about the functional groups. It was found that some metal(oid) ions (As, Ni, Pb, Zn) were coordinated through the mercaptan group, while other metal(oid)s (Al, Cd, Cu, Fe, Hg, Mn) were apparently bonded to oxygen atoms. A low-cost and effective solid phase retention system for extraction of heavy metals from aqueous solutions was thus developed. - Graphical abstract: Nitric acid-etched coal fly ash labelled with 2-mercaptoethanol or thioglycolic acid was intended for the retention of heavy metals. The bonding characteristics between the organic compounds with the solid support, as well as with the metal ions, were evaluated using surface analytical techniques. - Highlights: • Coal fly ashes were organically-functionalized. • Organically-functionalized coal fly ashes were spectrometrically characterized. • Organically-functionalized coal fly ashes can be used as an effective solid sorbent for metal(oid)s. • This retention

  13. High pressure Raman spectroscopic study of the effects of n-ethylamines and water on the 2-nitropropane/Nitric acid system

    Energy Technology Data Exchange (ETDEWEB)

    Gobin, Cedric; Petitet, Jean Pierre [Laboratoire d' Ingenierie des Materiaux et des Hautes Pressions, CNRS, Institut Galilee, Universite Paris XIII, 99 av. J-B Clement, 93430 Villetaneuse (France)

    2005-12-01

    High pressure Raman spectroscopy measurements in a diamond anvil cell (0-10 GPa) on 2-nitropropane/nitric acid/X (X=triethylamine, diethylamine, and water) ternary systems and 2-nitropropane/nitric acid/water/Y (Y=triethylamine and diethylamine) quaternary systems are reported. The modifications of the chemical behavior of the 2-nitropropane/nitric acid model system, induced by the presence of triethylamine, diethylamine, and/or water, were studied at ambient and high pressure. At ambient pressure, the ionization of the nitric acid has been observed with each of the additives. Moreover, in the case of ethylamines, new peaks have been observed and the hypothesis of a 2-nitropropane/ethylamine complex is advanced. At high pressure, the decomposition of the 2-nitropropane/nitric acid system, with an oxygen balance near zero, has been observed only in presence of triethylamine. The role of each additive to the 2-nitropropane/nitric acid system in the modification of the respective reducing and oxidizing character of the components, and in the reactivity of the system, is discussed. Several hypotheses are advanced concerning the sensitizing effect of the additives on the 2-nitropropane/nitric acid system. (Abstract Copyright [2005], Wiley Periodicals, Inc.)

  14. Corrosion of Selected Materials in Boiling Sulfuric Acid for the Nuclear Power Industries

    International Nuclear Information System (INIS)

    Iodine sulfur (IS) process is one of the promising processes for a hydrogen production by using a high temperature heat generated by a very high temperature gas cooled reactor(VHTR) in the nuclear power industries. Even though the IS process is very efficient for a hydrogen production and it is not accompanied by a carbon dioxide evolution, the highly corrosive environment of the process limits its application in the industry. Corrosion tests of selected materials were performed in sulfuric acid to select appropriate materials compatible with the IS process. The materials used in this work were Fe-Cr alloys, Fe-Ni-Cr alloys, Fe-Si alloys, Ni base alloys, Ta, Ti, Zr, SiC, Fe-Si, etc. The test environments were 50 wt% sulfuric acid at 120 .deg. C and 98 wt% at 320 .deg. C. Corrosion rates were measured by using a weight change after an immersion. The surface morphologies and cross sectional areas of the corroded materials were examined by using SEM equipped with EDS. Corrosion behaviors of the materials were discussed in terms of the chemical composition of the materials, a weight loss, the corrosion morphology, the precipitates in the microstructure and the surface layer composition

  15. The redox chemistry of neptunium in γ-irradiated aqueous nitric acid in the presence of an organic phase

    International Nuclear Information System (INIS)

    The radiolytic changes in oxidation state for solutions of initially Np(V) and/or Np(VI) were investigated by gamma-irradiation in conjunction with UV/Vis spectroscopy of the aqueous phase. Samples were irradiated in varying concentrations of nitric acid, and with or without the presence of 30 % TBP in dodecane. At short irradiation times Np(V) was oxidized to Np(VI), even in the presence of the organic phase. Upon the radiolytic production of sufficient amounts of nitrous acid, reduction of Np(VI) to Np(V) occurred in both phases. This was accompanied by stripping of the previously extracted Np(VI). Nitric acid concentrations of 6 M mitigated this reduction. (author)

  16. The effect of fatty acid surfactants on the uptake of nitric acid to deliquesced NaCl aerosol

    Directory of Open Access Journals (Sweden)

    M. Ammann

    2008-09-01

    Full Text Available Surface active organic compounds have been observed in marine boundary layer aerosol. Here, we investigate the effect such surfactants have on the uptake of nitric acid (HNO3, an important removal reaction of nitrogen oxides in the marine boundary layer. The uptake of gaseous HNO3 on deliquesced NaCl aerosol was measured in a flow reactor using HNO3 labelled with the short-lived radioactive isotope 13N. The uptake coefficient γ on pure deliquesced NaCl aerosol was γ=0.5±0.2 at 60% relative humidity and 30 ppb HNO3(g. The uptake coefficient was reduced by a factor of 5–50 when the aerosol was coated with saturated linear fatty acids with carbon chain lengths of 18 and 15 atoms in monolayer quantities. In contrast, neither shorter saturated linear fatty acids with 12 and 9 carbon atoms, nor coatings with the unsaturated oleic acid (C18, cis-double bond had a detectable effect on the rate of HNO3 uptake. It is concluded that it is the structure of the monolayers formed, which determines their resistance towards HNO3 uptake. Fatty acids (C18 and C15, which form a highly ordered film in the so-called liquid condensed state, represent a significant barrier towards HNO3 uptake, while monolayers of shorter-chain fatty acids (C9, C12 and of the unsaturated oleic acid form a less ordered film in the liquid expanded state and do not hinder the uptake. Similarly, high contents of humic acids in the aerosol, a structurally inhomogeneous, quite water soluble mixture of oxidised high molecular weight organic compounds did not affect HNO3 uptake. As surfactant films on naturally occurring aerosol are expected to be less structured due to their chemical inhomogeneity, it is likely that their inhibitory effect on HNO3 uptake is smaller than that observed here for the C15 and C18 fatty acid monolayers.

  17. Electrolytic destruction of nitric acid in various reprocessing streams of fast breeder reactor fuels

    International Nuclear Information System (INIS)

    The salting concentration of Nitric acid to Reprocessing Plants of FBR fuels is 4 M HNO3,. Adjustment of the free acidity of the Dissolver solution from 8 to 10 M HNO3, to a concentration of 4M HNO3 is done cathodically. This would increase the throughput of the plant. The concentration of HNO3 in first cycle raffinate, HAW, that would be stored in SS tanks (interim storage before vitrification) should be less than 6 M; otherwise severe corrosion problems would occur. The HAW discharged in FBR fuel reprocessing plants would contain around 4M HNO3. This has to be reduced to around 0.4M HNO3 in order to effect efficient reduction in waste volume, by evaporation. This has been achieved in the catalytic reduction of HNO3 to oxides of nitrogen. Current efficiency in the 1 L level is around 46%. Conventionally, HNO3 in raffinates are destroyed by addition of formaldehyde. The disadvantages of this method are highlighted in this paper. Addition of 0.01 M Cu2+ is found to completely avoid critical concentration of HNO3 below which nitrate ions will not be destroyed; instead H2 gas would be evolved. The results of these experiments in a simulated HAW are also included in this paper. Operation and the results of electrolytic destruction of HNO3 in simulated raffinate in a scaled-up SS equipment of 3.5 L capacity are also described in this payer. (author)

  18. Photolysis of Nitric Acid and Nitrate on Natural and Artificial Surfaces.

    Science.gov (United States)

    Ye, Chunxiang; Gao, Honglian; Zhang, Ning; Zhou, Xianliang

    2016-04-01

    Photolysis of nitric acid and nitrate (HNO3/nitrate) was investigated on the surfaces of natural and artificial materials, including plant leaves, metal sheets, and construction materials. The surfaces were conditioned in the outdoor air prior to experiments to receive natural depositions of ambient HNO3/nitrate and other atmospheric constituents. The photolysis rate constant (JHNO3(s)) of the surface HNO3/nitrate was measured based on the production rates of nitrous acid (HONO) and nitrogen oxides (NOx). The JHNO3(s) values, from 6.0 × 10(-6) s(-1) to 3.7 × 10(-4) s(-1), are 1 to 3 orders of magnitude higher than that of gaseous HNO3. The HONO was the major product from photolysis of HNO3/nitrate on most plant leaves, whereas NOx was the major product on most artificial surfaces. The JHNO3(s) values decreased with HNO3/nitrate surface density and could be described by a simple analytical equation. Within a typical range of HNO3/nitrate surface density in the low-NOx forested areas, photolysis of HNO3/nitrate on the forest canopy can be a significant source for HONO and NOx for the overlying atmosphere. PMID:26936001

  19. A quantitative test of infrared optical constants for supercooled sulphuric and nitric acid droplet aerosols

    Directory of Open Access Journals (Sweden)

    R. Wagner

    2003-05-01

    Full Text Available In situ Fourier transform infrared (FTIR extinction spectra of supercooled H2SO4/H2O and HNO3/H2O solution droplets were recorded in the large coolable aerosol chamber AIDA (Aerosol Interactions and Dynamics in the Atmosphere of Forschungszentrum Karlsruhe for a range of aerosol compositions and at temperatures extending down to 192 K. The measured spectra were quantitatively analysed in terms of aerosol composition and mass concentration by using Mie theory in combination with published refractive index data as input parameters. Simultaneously, total sulphuric acid and nitric acid mass concentrations from filter analysis and total water concentrations measured with the Lyman-a hygrometer of Forschungszentrum Jülich were used to calculate the aerosol composition at thermodynamic equilibrium inside the aerosol chamber. By comparing these measured aerosol parameters with those retrieved from the analysis of the FTIR spectra, the accuracy of the literature data sets of refractive indices could be assessed. In summary, four data sets were tested in the H2SO4/H2O system as well as two data sets in the HNO3/H2O system, partly revealing significant discrepancies in the retrieved aerosol properties. Potential explanations for these differences are discussed in this paper.

  20. A safer and flexible method for the oxygen functionalization of carbon nanotubes by nitric acid vapors

    Energy Technology Data Exchange (ETDEWEB)

    Santangelo, Saveria, E-mail: saveria.santangelo@unirc.it [Dipartimento di Ingegneria Civile, dell’Energia, dell’Ambiente e dei Materiali (DICEAM), Università “Mediterranea”, 89122 Reggio Calabria (Italy); Piperopoulos, Elpida [Dipartimento di Ingegneria Eletronica, Chimica ed Ingegneria Industriale (DIECII), Università di Messina, 98166 Messina (Italy); Fazio, Enza [Dipartimento di Fisica e di Scienze della Terra (DFST), Università di Messina, 98166 Messina (Italy); Faggio, Giuliana [Dipartimento di Ingegneria dell’Informazione, delle Infrastrutture e dell’Energia Sostenibile (DIIES), Università “Mediterranea”, 89122 Reggio Calabria (Italy); Ansari, Shabana [Dipartimento di Ingegneria Eletronica, Chimica ed Ingegneria Industriale (DIECII), Università di Messina, 98166 Messina (Italy); Lanza, Maurizio [Istituto per i Processi Chimico Fisici (IPCF) del CNR, 98158 Messina (Italy); Neri, Fortunato [Dipartimento di Fisica e di Scienze della Terra (DFST), Università di Messina, 98166 Messina (Italy); Messina, Giacomo [Dipartimento di Ingegneria dell’Informazione, delle Infrastrutture e dell’Energia Sostenibile (DIIES), Università “Mediterranea”, 89122 Reggio Calabria (Italy); Milone, Candida [Dipartimento di Ingegneria Eletronica, Chimica ed Ingegneria Industriale (DIECII), Università di Messina, 98166 Messina (Italy)

    2014-06-01

    The functionalization by nitric acid vapors at azeotropic concentration has been recently proposed to eliminate drawbacks of the widely utilized liquid phase functionalization method. This work suggests to exploit the so-called “salt effect” to improve the vapor phase oxidation method in terms of safety and flexibility. Increasing the relative volatility of acid, the addition of Mg(NO{sub 3}){sub 2} salt to the HNO{sub 3} + H{sub 2}O solution allows (i) obtaining vapors with HNO{sub 3} at the azeotropic concentration from a more diluted liquid solution (i.e. operating under safer conditions), and (ii) varying the concentration of HNO{sub 3} in the vapor phase even above the azeotropic concentration limit (with improved process flexibility). High-resolution transmission electron microscopy, thermo-gravimetry, Raman spectroscopy and X-ray photoemission spectroscopy systematic analyses are carried out on pristine and oxidized nanotubes in order to assess their functionalization degree, surface chemistry and structural evolution. The most relevant finding of this preliminary study is that the nanotube functionalization extent increases linearly with the HNO{sub 3} vapor concentration.

  1. PC-88A - impregnated polymeric beads. Preparation, characterization and application for extraction of Pu(IV) from nitric acid medium

    International Nuclear Information System (INIS)

    The extractant-impregnated polymeric beads (EIPBs), containing polyethersulfone as base polymer and 2-ethylhexyl phosphonic acid mono-2-ethylhexyl ester (PC-88A) as an extractant, were prepared by phase inversion method. These EIPBs were characterized by FTIR, TGA and SEM techniques. The beads were found to have excellent acid stability, since these did not exhibit any structural deformation or loss of the extractant into aqueous nitric acid solution (6 M), for a period of 15 d. The feasibility of Pu(IV) extraction, using these beads, from nitric acid solution was tested by batch equilibration method. Parametric dependence of Pu(IV) extraction on experimental variables, like strength of nitric acid, equilibration time, Pu(IV) concentration, etc., was investigated. The present study also addressed the important practical issues, like maximum loading capacity and the reusability of these beads. Under optimized conditions, equilibrium capacity and maximum loading capacity for Pu(IV) were found to be 2.03 and 7.50 mg per gram of the swollen beads, respectively. The reusability of the beads was also ascertained by repetitive extraction-stripping of Pu(IV) up to 7 cycles of operation, without significant change in their extraction performance. The extraction of Pu(IV) by the blank polymeric beads was observed to be almost negligible, under the similar experimental conditions. (orig.)

  2. Inducible nitric oxide synthase links NF-κB to PGE2 in polyunsaturated fatty acid altered fibroblast in-vitro wound healing

    OpenAIRE

    Turek John J; Jia Yi

    2005-01-01

    Abstract Background This study investigated mechanisms of altered fibroblast collagen production induced by polyunsaturated fatty acids. 3T3-Swiss fibroblasts were grown in medium containing either eicosapentaenoic or arachidonic acid. The effects of nuclear factor-kappaB activation by lipopolysaccharide on inducible nitric oxide synthase, nitric oxide, prostaglandin E2, collagen production, and in-vitro wound healing were studied. Results Eicosapentaenoic acid treated cells produced less pro...

  3. Extraction of palladium from nitric acid medium by commercial resins with phosphinic acid, methylene thiol and isothiouronium moieties attached to polystyrene-divinylbenzene

    International Nuclear Information System (INIS)

    Commercially available polystyrene-divinylbenzene (PS-DVB) resins functionalized with isothiouronium (Tulsion CH-95), phosphinic acid (Tulsion CH-96) and methylene thiol (Tulsion CH-97) moieties have been used for separating palladium from nitric acid medium. Extraction of palladium has been studied as a function of time, concentration of nitric acid and palladium. The distribution coefficients (Kd, ml/g) of palladium on sulfur based resins (Tulsion CH-95 and Tulsion CH-97) are higher (5000-104 ml/g in 0.1M nitric acid) than on Tulsion CH-96 resin and decrease with increasing concentration of nitric acid. The initial rate of extraction of palladium by Tulsion CH-95 and Tulsion CH-97 resins was very rapid and the time required for the establishment of equilibrium was a function of palladium concentration in the aqueous phase. The rate data could be fitted by a second order rate equation and the magnitude of rate constant for the extraction of palladium by these resins (∼102M-1 x min-1) decreased in the order of: Tulsion CH-95 > Tulsion CH-97 > Tulsion CH-96. The extraction isotherms of Tulsion CH-95 were fitted by Langmuir adsorption model and the coefficients were obtained by regression. The extraction capacity of palladium on Tulsion CH-95 was found to be ∼20 mg/g at 3M nitric acid. Column experiments have been conducted and the data were fitted using Thomas model. A column utilization of 75% was achieved for the extraction of palladium by Tulsion CH-95 resin. (author)

  4. Oxidation of hydroxylamine by nitrous and nitric acids. Model development from first principle SCRF calculations.

    Science.gov (United States)

    Raman, Sumathy; Ashcraft, Robert W; Vial, Marc; Klasky, Marc L

    2005-09-29

    Ab initio molecular orbital calculations have been performed to develop an elementary reaction mechanism for the autocatalytic and scavenging reactions of hydroxylamine in an aqueous nitric acid medium. An improved understanding of the titled reactions is needed to determine the "stability boundary of hydroxylamine" for safe operations of the plutonium-uranium reduction extraction (PUREX) process. Under the operating conditions of the PUREX process, namely, 6 M nitric acid, the reactive forms of hydroxylamine are NH2OH, NH3OH+, and the complex NH3OH.NO3, and those of nitrous acid are NO+, H2ONO+, N2O4, N2O3, NO2, and NO. High-level CBSQB3/IEFPCM and CBSQB3/COSMO calculations were performed using GAUSSIAN03 to investigate the energy landscape and to explore a large number of possible ion-ion, ion-radical, ion-molecule, radical-radical, radical-molecule, and molecule-molecule pathways available to the reactive forms of the reactants in solution. It was found that in solution the autocatalytic generation of nitrous acid proceeds through free radical pathways at low-hydroxylamine concentrations from unprotonated NH2OH via hydrogen abstraction. At high [NH3OH+], we suggest a possible involvement of the NH3ONO+ intermediate via the reaction NH2ONO + NO2 --> HNO + HONO + NO. The NH3ONO+ intermediate, in turn, is formed favorably via the ion-ion reactions of NH3OH+ with NO+ and/or the reaction between NO+ and hydroxylammonium nitrate (HAN). The intermediates involved in the scavenging reaction of nitrous acid by hydroxylamine are NH3ONO+, NH2ONO, NH2(NO)O, NH(NO)OH, and HONNOH and the rate-determining step is the 1,2-NO migration in NH2ONO leading to NH2(NO)O. Reactions NH2ONO --> NH2(NO)O and NH2(NO)O --> NH(NO)OH were studied with two explicit water molecules and the results are discussed in the context of the importance of the explicit treatment of solvent in the determination of the energetics and mechanism of these processes. The rate constants for the reactions were

  5. Task-specific ionic liquids incorporating alkyl phosphate cations for extraction of U(VI) from nitric acid medium. Synthesis, characterization, and extraction performance

    International Nuclear Information System (INIS)

    Imidazole-based task-specific ionic liquids designed to extract U(VI) from nitric acid medium were synthesized through the introduction of tributyl phosphate functional group in cationic of these ionic liquids. Their structures were confirmed by Fourier transform infrared spectrometer, nuclear magnetic resonance spectrum and element analysis. These task-specific ionic liquids can be used simultaneously as solvents and extractants for extracting U(VI) in nitric acid medium. Preliminary extraction data showed that they could be efficiently used to extract U(VI) in nitric acid medium at room temperature. (author)

  6. TBP 20% diluent/H N O3/H2 O liquid-liquid extraction system: equilibrium data normalization of nitric acid, ruthenium and zirconium

    International Nuclear Information System (INIS)

    The extraction behavior of nitric acid, nitrosyl ruthenium nitrate and zirconium hydroxide nitrate in the system tri-n-butyl phosphate (TBP) 20% -diluent was studied. The main purpose was to obtain enough data to elaborate process flowsheets for the treatment of irradiated uranium fuels. During the runs, the equilibrium diagrams of nitric acid, ruthenium and zirconium were settled. From the achieved data, the influence of nitric acid, ruthenium, zirconium and nitrate ions concentration in the aqueous phase was checked. Furthermore, the density and the surface tension of the aqueous and organic phases were determined, gathering the interfacial tension after the contact between the phases. (author)

  7. Bis(2-ethylhexyl)diglycolamic acid for the mutual separation of Europium (III) and Americium (III) from citric acid - nitric acid medium

    International Nuclear Information System (INIS)

    High-level liquid waste arises from fast reactor fuel reprocessing contains significant quantities of lanthanides and trivalent minor actinides. Recently, the partitioning of minor actinides from fast reactor-high active waste (FR-HAW) using a TRUEX solvent, composed of a solution of 0.2 M octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO)-1.2 M tri-n-butylphosphate (TBP) in n-dodecane is demonstrated. A new stripping formulation composed of a solution of 0.1 M citric acid in 0.1 M nitric acid was employed for back extraction of trivalents from the loaded TRUEX solvent. Thus the mutual separation lanthanides and actinides requires a suitable extractant for separating them from citric acid medium

  8. Effect of ascorbic acid supplementation on nitric oxide metabolites and systolic blood pressure in rats exposed to lead

    Directory of Open Access Journals (Sweden)

    Mohammad Amani

    2010-01-01

    Full Text Available Background: Extended exposure to low levels of lead causes high blood pressure in human and laboratory animals. The mechanism is not completely recognized, but it is relatively implicated with generation of free radicals, oxidant agents such as ROS, and decrease of available nitric oxide (NO. In this study, we have demonstrated the effect of ascorbic acid as an antioxidant on nitric oxide metabolites and systolic blood pressure in rats exposed to low levels of lead. Materials and Methods: The adult male Wistar rats weighing 200-250 g were divided into four groups: control, lead acetate (receiving 100 ppm lead acetate in drinking water, lead acetate plus ascorbic acid (receiving 100 ppm lead acetate and 1 g/l ascorbic acid in drinking water, and ascorbic acid (receiving 1 g/l ascorbic acid in drinking water groups. The animals were anesthetized with ketamin/xylazine (50 and 7 mg/kg, respectively, ip and systolic blood pressure was then measured from the tail of the animals by a sphygmomanometer. Nitric oxide levels in serum were measured indirectly by evaluation of its stable metabolites (total nitrite and nitrate (NOc. Results: After 8 and 12 weeks, systolic blood pressure in the lead acetate group was significantly elevated compared to the control group. Ascorbic acid supplementation could prevent the systolic blood pressure rise in the lead acetate plus ascorbic acid group and there was no significant difference relative to the control group. The serum NOc levels in lead acetate group significantly decreased in relation to the control group, but this reduction was not significantly different between the lead acetate plus ascorbic acid group and the control group. Conclusion: Results of this study suggest that ascorbic acid as an antioxidant prevents the lead induced hypertension. This effect may be mediated by inhibition of NOc oxidation and thereby increasing availability of NO.

  9. Amides as phase modifiers for N,N'-tetraalkylmalonamide extraction of actinides and lanthanides from nitric acid solutions

    International Nuclear Information System (INIS)

    The N,N'-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'-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

  10. The effect of gamma irradiation on the nitric acid solution as washing agent used in Ru-U extraction process

    International Nuclear Information System (INIS)

    The continuous extraction of uranium was carried out in a 12 -stage bank of mixer-settlers using a 30% volume Tbp-kerosene mixture solvent. The uranyl nitrate solution of 200 g U/l containing 11 mg/l of ruthenium as impurity was fed to the mixer settlers at 7th stage at 75 ml/h flow rate. The 30% volume Tbp-kerosene solvent was introduced at 1st stage at 150 ml/h flow rate, while the nitric acid washing solution already gamma irradiated at 103, 105, 107, 108 rads respectively was fed at 12th stage at 56 ml/h flow rate. Extraction time was 6 hours, and the stirring was done at 2300 rpm. The experiments showed that gamma irradiation caused the degradation of nitric acid which was shown by the decrease in its acidity. Increasing radiation dose to the nitric acid solution resulted in the decrease of uranium recovery and the FDRu-U. At the lowest radiation dose (i.e. 103 rad) the uranium recovery and FDRu-U obtained respectively were found to be 96.37% and 2.19, while that at the highest radiation dose (i.e. 108 rad) they were 88.20% and 2.01 respectively

  11. Comparative analysis of the effect of pretreating aspen wood with aqueous and aqueous-organic solutions of sulfuric and nitric acid on its reactivity during enzymatic hydrolysis

    DEFF Research Database (Denmark)

    Dotsenko, Gleb; Osipov, D. O.; Zorov, I. N.;

    2016-01-01

    The effect of aspen wood pretreatment methods with the use of both aqueous solutions of sulfuric and nitric acids and aqueous-organic solutions (ethanol, butanol) of sulfuric acid (organosolv) on the limiting degree of conversion of this type of raw material into simple sugars during enzymatic...... hydrolysis are compared. The effects of temperature, acid concentration, composition of organic phase (for sulfuric acid), and pressure (for nitric acid) on the effectiveness of pretreatment were analyzed. It is shown that the use of organosolv with 0.5% sulfuric acid allows us to increase the reactivity of...

  12. Extraction behavior of molybdenum and zirconium with diisodecylphosphoric acid from nitric acid solution

    International Nuclear Information System (INIS)

    This study was performed mainly from the viewpoint of consumption of diisodecylphosphoric acid (DIDPA) by the extracted Mo and Zr to estimate extraction capacities. The number of DIDPA molecules consumed per one extracted Mo atom was four when the concentration of Mo in the aqueous phase was less than 10-3M and it decreased with increasing Mo concentration. Two molecules of DIDPA were consumed per one extracted Zr atom when the Zr concentration was high. Dependencies of the distribution ratio of Mo on the concentrations of Mo, DIDPA and HNO3 are also described. (author) 15 refs.; 7 figs

  13. Study of the nitric acid influence on the production of Ce O2 with high specific surface area

    International Nuclear Information System (INIS)

    The cerium oxide (Ce O2) main characteristics for use as catalyst in an exhaust gases purification system are: high specific surface area (approximately 30 m2/g after calcination at 800 deg C/ 2 hs), and thermal stability. The Ce O2 powders obtained by conventional route, i.e., precipitation, and submitted high temperature (800 deg C) heat treatments, showed low specific surface area. In this work nitric acid effects on the Ce O2 surface area values were investigated. The variables studied were nitric acid concentration, humidity content in the raw material, re pulp after leaching, addition of hydrogen peroxide (H2 O2) and starting material specific surface area. By this process, it was possible to obtain powders with specific surface area larger than 40 m2/g, after treatment at 800 deg C during two hours. (author)

  14. Electrodeposition of ruthenium, rhodium and palladium from nitric acid and ionic liquid media: Recovery and surface morphology of the deposits

    International Nuclear Information System (INIS)

    Research highlights: → Platinum group metals are man-made noble metals. → Electrochemical recovery of fission platinoids. → Recovery from nitric acid medium. → Recovery from ionic liquid medium. → Platinoids with exotic surface morphologies. - Abstract: Electrodeposition is a promising technique for the recovery of platinum group metals with unique surface morphologies. The electrodeposition of palladium, ruthenium and rhodium from aqueous nitric acid, and non-aqueous 1-butyl-3-methylimidazolium chloride ionic liquid medium was studied at stainless steel electrode. The surface morphology and elemental composition of the resultant deposit were probed by scanning electron microscopy (SEM) and energy dispersive X-ray (EDS) analysis. Deposits with diverse surface morphologies and metal compositions were obtained by varying the composition of the electrolytic medium and applied potential. The results demonstrate the possibility of tailoring the morphologies of PGMs by controlling the composition and potential needed for electrodeposition.

  15. Effect of nitric acid leaching on the separation of U and common impurities from solid (U, Pu, Ag) analytical waste

    International Nuclear Information System (INIS)

    The effect of leaching a solid analytical waste of (U,Pu)O2 and AgCl with concentrated nitric acid for different time intervals was studied. The amount of Pu/U leached was found to be nearly same in the selected time interval 15-90 minutes. Hence the effect of multi-step leaching on the dissolution of U/Pu was studied. After four steps of 15 minute leaching, entire uranium was leached along with about 3% Pu. Later keeping the time constant, the effect of nitric acid molarity on the leaching of U and Pu was investigated. The leaching of impurities was found to decrease with each step. However the amounts of rare earths and Ag leached were found to be negligible. (author)

  16. (U, Th, RE) hydroxide dissolution of Bangka's monazite base decomposition, using nitric acid

    International Nuclear Information System (INIS)

    The (U, Th, RE) hydroxide dissolution experiment on Bangka's monazite base decomposition product using nitric acid (HNO3) reagent has been done. The uses of HNO3 for (U, Th, RE)NO3 solution product can do extraction with TBP-Kerosene to take impurity of Th in the end product of RE. The solution use of HCl gave end product RE with high Th as 1000 - 1500 ppm. The aim of the experiment was to find a good conditions of dissolution with applied parameter were HNO3 normality, amount of redactor, temperature and dissolution time respectively. This experiment used feed (U, Th, RE) hydroxide as product -200 mesh Bangka monazite base decomposition. The amount of feed for a time experiment is 50 gram wet, 36% of water content, the compartment volume of reagent / weight of feed is 1. The results gave a good experiment conditions i.e. HNO3 14 N, amount of redactor 20 ml H2O2, at room temperature and a hour dissolution time respectively. Such conditions gave the recovery of U 53.14 %; Th 88.98 %; RE2O3 70.03% and P2O5 53.89 %

  17. Dissolution of plutonium dioxide in nitric acid media by silver(II) electroreduction

    International Nuclear Information System (INIS)

    Oxidative dissolution of plutonium dioxide with electrogenerated silver(II) was undertaken first on an analytical scale in order to discover the parameters controlling this dissolution process and to prove the feasibility of the technique for 300 grams of material. The influence on the rate of PuO2 dissolution of the following parameters was studied: mass of PuO2, current density, total concentration of silver ion, nitric acid concentration, temperature, and agitation efficiency. The results demonstrate that: 1. the limiting step of the dissolution process is the electrogeneration of silver(II); 2. the dissolution of PuO2 can be achieved with a good current efficiency; 3. the best temperature range is 30±100C; 4. the optimum [HNO3] is 4 to 6 M; 5. the plutonium(VI) solution up to 500 g l-1 can be prepared. A six litres capacity thermostated glass electrolyser was built which consists of two separated compartments inlcuding: 1. an anodic compartment equipped with a cylindrical platinum grid electrode (area, 1000 cm2) and a tantalum propeller, and 2. a cathodic compartment of 0.2 litre capacity consisting of an aluminium silicate diaphragm with a tantalum rod cathode. Quantitative dissolutions of 300 g of PuO2 in 4 M HNO3 were performed for 2 h at an applied current of 60 A. (orig.)

  18. Evaluation of anion exchange resins for plutonium-uranium separations in nitric acid

    International Nuclear Information System (INIS)

    Pellicular, macroreticular and microreticular (gel type) anion exchange resins were compared for separation of plutonium from nitric acid solutions of mixed plutonium-uranium. All the macroreticular resins were 20 to 50 mesh beads. Dowex 1-X4 gel resin was 50 to 80 mesh beads. The resins were held in glass columns with coarse glass frits at the bottom of the columns. The top of the columns contained 50 ml reservoirs. The flow rates were controlled at 4 cm3.min-1.cm-2. One-centimeter bore columns with 15-cm resin bed heights were used for the plutonium elution and breakthrough capacity experiments, whereas 1.7 cm bore columns with 20 cm bed heights were used for the uranium washing experiments. As Pellionex SAX (pellicular resin) and Amberlite IRA-93 (weak base macroreticular anion exchange resin) were found to have better uranium washing and plutonium eluating characteristics than any of the resins tested. However, the capacity of the pellicular resin was much lower than that of the other resins. (T.G.)

  19. Investigations of the inhibition of copper corrosion in nitric acid solutions by ketene dithioacetal derivatives

    Science.gov (United States)

    Fiala, A.; Chibani, A.; Darchen, A.; Boulkamh, A.; Djebbar, K.

    2007-10-01

    Ketene dithioacetal derivatives, namely 3-[bis(methylthio)methylene] pentane-2,4-dione ( 1), 3-(1,3-dithian-2-ylidene) pentane-2,4-dione ( 2) and 3-(1,3-dithiolan-2-ylidene) pentane-2,4-dione ( 3) were synthesized and their respective capacity to inhibit copper corrosion in 3 M HNO 3 was investigated by means of weight loss, potentiodynamic polarization, scanning electron microscopy (SEM) and energy dispersive X-ray fluorescence (XRF). The obtained results indicate that the addition of these compounds significantly decreases the corrosion rate. Potentiodynamic polarization studies clearly showed that the inhibition efficiency increases with increasing concentration of the investigated compounds at a fixed temperature, but decreases with increasing temperature. These results on the whole showed that the studied substances are good cathodic inhibitors for copper corrosion in nitric acid medium. SEM and energy dispersive X-ray (EDAX) examination of the copper surface revealed that these compounds prevented copper from corrosion by adsorption on its surface to form a protective film, which acts as a barrier to aggressive agents. The presence of these organic compounds adsorbed on the electrode surface was confirmed by XRF investigations.

  20. Uranium removal from nitric acid raffinate solution by solvent immobilized PVC cement

    International Nuclear Information System (INIS)

    The present work deals with uranium removal from a nitric acid raffinate (waste) solution using prepared solvent (tri-butyl phosphate, TBP) immobilizing PVC cement (SIC) as a suitable adsorbent. The studied relevant factors affecting uranium adsorption onto SIC adsorbent involved; contact time, solution molarity, initial uranium concentration and temperature. The obtained adsorption isotherm of uranium onto the SIC adsorbent was fitted to Langmuir, Freundlich and Dubinin-Radushkeviech (D-R) adsorption models. The results showed that the obtained equilibrium data fitted well the Langmuir isotherm. Additionally, it was found that the adsorption process obeys the pseudo second-order kinetic model. On the other hand, the calculated theoretical capacity of our prepared SIC adsorbent reached about 17 g U/kg SIC. Uranium adsorption from the studied raffinate solution was carried out applying the attained optimum conditions. The obtained data showed that 58.4 mg U/5 g SIC were adsorbed. However, using of 2 M HNO3 solution as an eluent, 93 (54.3 mg U) from the adsorbed amount were eluted. (author)

  1. The inhibited effect of some tetrazolic compounds towards the corrosion of brass in nitric acid solution

    International Nuclear Information System (INIS)

    The effect of the addition of some tetrazolic type organic compounds: 1-phenyl-5-mercapto-1,2,3,4-tetrazole (PMT), 1,2,3,4-tetrazole (TTZ), 5-amino-1,2,3,4-tetrazole (AT) and 1-phenyl-1,2,3,4-tetrazole (PT) on the corrosion of brass in nitric acid is studied by weight loss, polarisation and electrochemical impedance spectroscopy (EIS) measurements. The explored methods gave almost similar results. Results obtained reveal that PMT is the best inhibitor and the inhibition efficiency (E%) follows the sequence: PMT > PT > AT > TTZ. Polarization measurements also indicated that tetrazoles acted as mixed-type inhibitors without changing the mechanism of the hydrogen evolution reaction. Partial π-charge on atoms has been calculated. Correlation between the highest occupied molecular orbital energy E HOMO and inhibition efficiencies was sought. The adsorption of PMT on the brass surface followed the Langmuir isotherm. Effect of temperature is also studied in the (25-50 deg. C) range

  2. The inhibited effect of some tetrazolic compounds towards the corrosion of brass in nitric acid solution

    Energy Technology Data Exchange (ETDEWEB)

    Mihit, M. [Laboratoire de Chimie-Physique, Equipe de Chimie Moleculaire and Corrosion, Faculte des Sciences, Agadir B.P 8106 (Morocco); El Issami, S. [Laboratoire de Chimie-Physique, Equipe de Chimie Moleculaire and Corrosion, Faculte des Sciences, Agadir B.P 8106 (Morocco); Bouklah, M. [Laboratoire de Chimie des Eaux and Corrosion, Faculte des Sciences, Oujda (Morocco); Bazzi, L. [Laboratoire de Chimie-Physique, Equipe de Chimie Moleculaire and Corrosion, Faculte des Sciences, Agadir B.P 8106 (Morocco); Hammouti, B. [Laboratoire de Chimie des Eaux and Corrosion, Faculte des Sciences, Oujda (Morocco)]. E-mail: hammoutib@yahoo.fr; Ait Addi, E. [Laboratoire de Chimie-Physique, Equipe de Chimie Moleculaire and Corrosion, Faculte des Sciences, Agadir B.P 8106 (Morocco); Salghi, R. [Laboratoire de l' Environnement et Science de l' Eau, Ecole Nationale des Sciences Appliquees d' Agadir, B.P. 33/S, Agadir (Morocco); Kertit, S. [Laboratoire de Physico-Chimie des Materiaux, Ecole Normale Superieure-Takaddoum, Rabat (Morocco)

    2006-01-15

    The effect of the addition of some tetrazolic type organic compounds: 1-phenyl-5-mercapto-1,2,3,4-tetrazole (PMT), 1,2,3,4-tetrazole (TTZ), 5-amino-1,2,3,4-tetrazole (AT) and 1-phenyl-1,2,3,4-tetrazole (PT) on the corrosion of brass in nitric acid is studied by weight loss, polarisation and electrochemical impedance spectroscopy (EIS) measurements. The explored methods gave almost similar results. Results obtained reveal that PMT is the best inhibitor and the inhibition efficiency (E%) follows the sequence: PMT > PT > AT > TTZ. Polarization measurements also indicated that tetrazoles acted as mixed-type inhibitors without changing the mechanism of the hydrogen evolution reaction. Partial {pi}-charge on atoms has been calculated. Correlation between the highest occupied molecular orbital energy E {sub HOMO} and inhibition efficiencies was sought. The adsorption of PMT on the brass surface followed the Langmuir isotherm. Effect of temperature is also studied in the (25-50 deg. C) range.

  3. Characteristic of wet method of phosphorus recovery from polish sewage sludge ash with nitric acid

    Directory of Open Access Journals (Sweden)

    Gorazda Katarzyna

    2016-12-01

    Full Text Available Sewage Sludge Ash (SSA is a concentrated source of phosphorus and can be successfully recycled via a number of different routes. This paper presents research results on phosphorus recovery from differently combusted sewage sludge with the use of nitric acid extraction. Different SSA forms from Polish thermal utilization stations were compared. It was revealed that sewage treatment technology as well as combustion technology influence many physical and chemical parameters of ashes that are crucial for further phosphorus recovery from such waste according to the proposed method. Presented research defines extraction efficiency, characterized extracts composition and verifies the possibility of using SSA as cheaper and alternative sources of phosphorus compounds. Gdynia, Kielce and Kraków SSA have the best properties for the proposed technology of phosphorus recovery with high extraction efficiency greater than 86%. Unsuitable results were obtained for Bydgoszcz, Szczecin Slag and Warszawa SSA. Extraction process for Łódź and Szczecin Dust SSA need to be improved for a higher phosphorus extraction efficiency greater than 80%.

  4. Silver ion catalyzed cerium(IV) mediated electrochemical oxidation of phenol in nitric acid medium

    International Nuclear Information System (INIS)

    Mediated electrochemical oxidation (MEO) is one of the sustainable processes for organic pollutant destruction and has been employed for organic mineralization reactions by many researchers. In the MEO a metal ion capable of exhibiting redox behavior is oxidized from lower oxidation state to higher oxidation state by an electrochemical cell and subsequently used as an oxidant for mineralizing the toxic organics into CO2 and water. The net result is the consumption of electrical energy for organic mineralization. Therefore, the current efficiency is an important factor and maximizing the current efficiency is one of the ways of reducing the running cost of the MEO process. It has been reported in the literature that the current efficiency could be increased using a metal ion catalyst having a good redox potential. In this study Ce(IV) mediated electrochemical oxidation of phenol was carried out with silver ion catalyst. The current efficiency for the electro-oxidation of cerium(III) in nitric acid was found to be increased by the addition of silver ions. This mixed mediator system was tested for the oxidation of phenol in order to optimize the parameters for organic pollutant destruction. The mineralization efficiency calculated based on the CO2 evolution was found to be higher for silver catalyzed Ce(IV) mediated oxidation compared to the non-silver catalyzed system

  5. Heterogeneous formation of polar stratospheric clouds – Part 1: Nucleation of nitric acid trihydrate (NAT

    Directory of Open Access Journals (Sweden)

    C. R. Hoyle

    2013-03-01

    Full Text Available Satellite based observations during the Arctic winter of 2009/2010 provide firm evidence that, in contrast to the current understanding, the nucleation of nitric acid trihydrate (NAT in the polar stratosphere does not only occur on preexisting ice particles. In order to explain the NAT clouds observed over the Arctic in mid December 2009, a heterogeneous nucleation mechanism is required, occurring via immersion freezing on the surface of solid particles, likely of meteoritic origin. For the first time, a detailed microphysical modelling of this NAT formation pathway has been carried out. Heterogeneous NAT formation was calculated along more than sixty thousand trajectories, ending at Cloud Aerosol Lidar with Orthogonal Polarisation (CALIOP observation points. Comparing the optical properties of the modelled NAT with these observations enabled the thorough validation of a newly developed NAT nucleation parameterisation, which has been built into the Zurich Optical and Microphysical box Model (ZOMM. The parameterisation is based on active site theory, is simple to implement in models and provides substantial advantages over previous approaches which involved a constant rate of NAT nucleation in a given volume of air. It is shown that the new method is capable of reproducing observed PSCs very well, despite the varied conditions experienced by air parcels travelling along the different trajectories. In a companion paper, ZOMM is applied to a later period of the winter, when ice PSCs are also present, and it is shown that the observed PSCs are also represented extremely well under these conditions.

  6. Heterogeneous formation of polar stratospheric clouds – Part 1: Nucleation of nitric acid trihydrate (NAT

    Directory of Open Access Journals (Sweden)

    C. R. Hoyle

    2013-09-01

    Full Text Available Satellite-based observations during the Arctic winter of 2009/2010 provide firm evidence that, in contrast to the current understanding, the nucleation of nitric acid trihydrate (NAT in the polar stratosphere does not only occur on preexisting ice particles. In order to explain the NAT clouds observed over the Arctic in mid-December 2009, a heterogeneous nucleation mechanism is required, occurring via immersion freezing on the surface of solid particles, likely of meteoritic origin. For the first time, a detailed microphysical modelling of this NAT formation pathway has been carried out. Heterogeneous NAT formation was calculated along more than sixty thousand trajectories, ending at Cloud Aerosol Lidar with Orthogonal Polarization (CALIOP observation points. Comparing the optical properties of the modelled NAT with these observations enabled a thorough validation of a newly developed NAT nucleation parameterisation, which has been built into the Zurich Optical and Microphysical box Model (ZOMM. The parameterisation is based on active site theory, is simple to implement in models and provides substantial advantages over previous approaches which involved a constant rate of NAT nucleation in a given volume of air. It is shown that the new method is capable of reproducing observed polar stratospheric clouds (PSCs very well, despite the varied conditions experienced by air parcels travelling along the different trajectories. In a companion paper, ZOMM is applied to a later period of the winter, when ice PSCs are also present, and it is shown that the observed PSCs are also represented extremely well under these conditions.

  7. Electro-Oxidation of Concentrated Ce(Ⅲ) at Carbon Felt Anode in Nitric Acid Media

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Electro-oxidation of Ce( Ⅲ) to Ce( Ⅳ ) in parallel plate flow type electrolyzer divided with cation exchange membrane was carried out in nitric acid media at carbon felt anode under galvanostatic conditions. Carbon felt was used as an anode for its high specific surface area and high oxygen evolution overpotential. Pt coated Ti plates were used as cathcurrent efficiency (92%) until about 80% of Ce( Ⅲ) was oxidized. Then, oxygen evolution, accompanied by terminal voltage jump, took place, lowering current efficiency. Ce( Ⅲ ) was oxidized up to 90% with current efficiency of 62%. In this mode, strong carbon felt anode oxidation was observed. The wear out of carbon felt was 46% in six consequent runs (6 h of operation). After each run, carbon felt surface had to be renewed with slightly alkaline solution to remove carbon oxidation products and ensure regular operational conditions. When anode surface was blocked, oxygen evolution took place from the beginning of electrolysis due to higher actual current density. The wear out of carbon felt anode could be minimized by means of oxygen evolution prevention. In the case when electrolysis had been stopped before oxygen evolution started (at Ce( Ⅳ ) conversion of about 80% ), the wear out of anode was less than 2% during 6 consequent runs (4 h of operation).

  8. Effects of composite restorations on nitric oxide and uric acid levels in saliva

    Directory of Open Access Journals (Sweden)

    Nilgun Akgul

    2015-01-01

    Full Text Available Background and Aims: Dental materials that are used in dentistry should be harmless to oral tissues, and should, therefore, not contain any leachable toxic and diffusible substances capable of causing side effects. This study was intended to investigate the effects on salivary nitric oxide (NO and uric acid (UA levels after application of dental composite filling materials to healthy volunteers. Materials and Methods: A total of 52 individuals (32 female and 20 male participated in the study. Filtek Z250 composite filling material (3M ESPE, St Paul, MN, USA was applied to healthy volunteers. Saliva samples were collected before restoration (baseline and 1 h, 1-day, 7 days, and 30 days after restoration. NO concentrations were measured using the Griess reaction method, and UA was measured using an enzymatic method. Data were analyzed using repeated measures ANOVA and the Bonferroni post-hoc test (α =5%. Results: NO values increased statistically significant after 7 days (P 0.05. There was no correlation between NO and UA levels in saliva (P > 0.05. Conclusion: Composite resins activated the antioxidant system in saliva. However, further studies are now needed to confirm our findings and to permit a definitive conclusion.

  9. Development and performance evaluation of nano platinum coated titanium electrode for application in nitric acid medium

    Energy Technology Data Exchange (ETDEWEB)

    Rasmi, K.R.; Vanithakumari, S.C.; George, R.P.; Mallika, C.; Kamachi Mudali, U., E-mail: kamachi@igcar.gov.in

    2015-02-01

    Nano platinum coated titanium (NPCT) electrodes were developed using electrodeposition assisted hydrothermal method for application as electrodes in reprocessing plant under severe corrosive environment. After synthesis, the morphology of the NPCT electrode surface was characterized using Field emission scanning electron microscopy (FESEM). The phase and chemical state of the modified electrode was investigated using X-ray diffractometer (XRD) and X-ray photoelectron spectroscopy (XPS) respectively. The enhanced electrochemical activity of NPCT electrode was established by conducting hydrogen adsorption-desorption study and electrochemical oxygen reduction studies. The performance of the electrode was investigated by employing it as anode in cerium oxidation under an applied current of 0.1 A in 11.5 M nitric acid. Post performance analysis reveals the stability of the synthesized electrode. - Highlights: • Nano Pt covered Ti with higher electrochemical activity was synthesized. • Efficiency of nano Pt coated titanium was double than polycrystalline bulk Pt. • The coating was intact post experiment in very aggressive environment of HNO{sub 3}.

  10. Heterogeneous formation of polar stratospheric clouds - Part 1: Nucleation of nitric acid trihydrate (NAT)

    Science.gov (United States)

    Hoyle, C. R.; Engel, I.; Luo, B. P.; Pitts, M. C.; Poole, L. R.; Grooß, J.-U.; Peter, T.

    2013-09-01

    Satellite-based observations during the Arctic winter of 2009/2010 provide firm evidence that, in contrast to the current understanding, the nucleation of nitric acid trihydrate (NAT) in the polar stratosphere does not only occur on preexisting ice particles. In order to explain the NAT clouds observed over the Arctic in mid-December 2009, a heterogeneous nucleation mechanism is required, occurring via immersion freezing on the surface of solid particles, likely of meteoritic origin. For the first time, a detailed microphysical modelling of this NAT formation pathway has been carried out. Heterogeneous NAT formation was calculated along more than sixty thousand trajectories, ending at Cloud Aerosol Lidar with Orthogonal Polarization (CALIOP) observation points. Comparing the optical properties of the modelled NAT with these observations enabled a thorough validation of a newly developed NAT nucleation parameterisation, which has been built into the Zurich Optical and Microphysical box Model (ZOMM). The parameterisation is based on active site theory, is simple to implement in models and provides substantial advantages over previous approaches which involved a constant rate of NAT nucleation in a given volume of air. It is shown that the new method is capable of reproducing observed polar stratospheric clouds (PSCs) very well, despite the varied conditions experienced by air parcels travelling along the different trajectories. In a companion paper, ZOMM is applied to a later period of the winter, when ice PSCs are also present, and it is shown that the observed PSCs are also represented extremely well under these conditions.

  11. Plasma Formed in Argon, Acid Nitric and Water Used in Industrial ICP Torches

    Institute of Scientific and Technical Information of China (English)

    F. BENDJEBBAR; P. ANDRE; M. BENBAKKAR; D. ROCHETTE; S. FLAZI; D. VACHER

    2012-01-01

    Inductively coupled plasmas (ICPs) are used in spectrochemical analyses. The introduction of the sample by means of an aerosol are widely used. The introduction and the total evaporation of the aerosol is required in order to obtain a good repeatability and reproducibility of analyses. To check whether the vaporization of the aerosol droplets inside the plasma is completed, a solution could be used to compare the experimental results of the emission spectral lines with theoretical results. An accurate calculation code to obtain monatomic spectral lines intensities is therefore required, which is the purpose of the present paper. The mixtures of argon, water and nitric acid are widely used in spectrochemical analyses with ICPs. With these mixtures, we calculate the composition, thermodynamic functions and monatomic spectral lines intensities of the plasma at thermodynamic equilibrium and at atmospheric pressure. To obtain a self sufficient paper and also to allow other researchers to compare their results, all required data and a robust accurate algorithm, which is simple and easy to compute, are given.

  12. Passivity and passivity breakdown of 304L stainless steel in hot and concentrated nitric acid

    International Nuclear Information System (INIS)

    The objective of this study is to characterize the oxidation behavior of 304L stainless steel (SS) in representative conditions of spent nuclear fuel reprocessing, i.e. in hot and concentrated nitric acid. In these conditions the SS electrochemical potential is in the passive domain and its corrosion rate is low. However when the media becomes more aggressive, the potential may be shifted towards the trans-passive domain characterized with a high corrosion rate. Passivity and passivity breakdown in the trans-passive domain are of a major interest for the industry. So as to characterize these phenomenons, this work was undertaken with the following representative conditions: a 304L SS from an industrial sheet was studied, the media was hot and concentrated HNO3, long term tests were performed. First, the surface of an immersed 304L SS was characterized with several complementary techniques from the micro to the nanometer scale. Then oxidation kinetics was studied in the passive and in the trans-passive domain. The oxidation behavior was studied thanks to weight loss determination and surface analysis. Finally, oxidation evolution as a function of the potential was studied from the passive to the trans-passive domain. In particular, this allowed us to obtain the anodic curve of 304L SS in hot and concentrated and to define precisely the 304L SS limits of in such conditions. (author)

  13. A New Process Study on Comprehensive Utilization of NOx from Nitric Acid Plant

    Institute of Scientific and Technical Information of China (English)

    ZhouHou-zhen; LiangHua

    2003-01-01

    Based on studies of controlling NOx from nitric acid exhaust gas domestic and abroad, this paper has developed a new technique on removal of NOx and production of a by-product with high added value MnO2. Experiment shows, pyrolusite, whose valid composition is MnO2, of absorbing NOx has the following characteristics: quick, low cost, no secondary pollutant. Moreover, exhaust gas can attain the required standards. If the temperature of the pyrolusite serum is 30℃, pH=4, containing 90 g/L MnO2, the absorptivity for 3 000 mg/m3 NOx is 89.2%. Furthermore,few of the impurities in pyrolusite dissolve in the absorption mother solution. The purification cost of product is very low.The purity of end product MnO2 is more than 99. 995% after purifying. Therefore, it is workable for the new technique on economy and technology. There are also obvious environmental benefits and marked economic returns.

  14. Electronic spectra of plutonium ions in nitric acid and in lithium nitrate solutions

    International Nuclear Information System (INIS)

    The absorption spectra of plutonium ions in nitric acid have been described. There is a characteristic change in the absorption spectra of Pu v in lithium nitrate solutions. In 2 M-lithium nitrate a new peak at 969 nm and high absorption at 1200 nm are noticed. A decrease in the absorption by about 20% and the appearance of a new shoulder at 1120 nm in 6 M-lithium nitrate are found. There is no change in the spectrum in 4 M-lithium nitrate. The absorption spectra of plutonium ions in the spectral range 200 - 400 nm are interesting. All plutonium ions have an intense band in the region 250 - 260 nm as well as a less intense and rather diffuse band at 320 - 330 nm in lithium nitrate solutions the sharp band at 250 - 260 nm has disappeared. This suggests that this band is very sensitive to the environmental field. The band is probably produced by 5 Fq→ 5 fq-1 6 d transition as well as electron transfer. It is believed that the spectrum of Pu V at pH 6.5 represents the hydrolysis product Pu O2(O H). 9 fig., 4 tab

  15. Curcumin Derivatives as Green Corrosion Inhibitors for α-Brass in Nitric Acid Solution

    Science.gov (United States)

    Fouda, A. S.; Elattar, K. M.

    2012-11-01

    1,7- Bis-(4-hydroxy-3-methoxy-phenyl)-hepta-1,6-diene-4-arylazo-3,5-dione I-V have been investigated as corrosion inhibitors for α-brass in 2 M nitric acid solution using weight-loss and galvanostatic polarization techniques. The efficiency of the inhibitors increases with the increase in the inhibitor concentration but decreases with a rise in temperature. The conjoint effect of the curcumin derivatives and KSCN has also been studied. The apparent activation energy ( E a*) and other thermodynamic parameters for the corrosion process have also been calculated. The galvanostatic polarization data indicated that the inhibitors were of mixed-type, but the cathode is more polarized than the anode. The slopes of the cathodic and anodic Tafel lines ( b c and b a) are maintained approximately equal for various inhibitor concentrations. However, the value of the Tafel slopes increases together as inhibitor concentration increases. The adsorption of these compounds on α-brass surface has been found to obey the Frumkin's adsorption isotherm. The mechanism of inhibition was discussed in the light of the chemical structure of the undertaken inhibitors.

  16. Development and performance evaluation of nano platinum coated titanium electrode for application in nitric acid medium

    International Nuclear Information System (INIS)

    Nano platinum coated titanium (NPCT) electrodes were developed using electrodeposition assisted hydrothermal method for application as electrodes in reprocessing plant under severe corrosive environment. After synthesis, the morphology of the NPCT electrode surface was characterized using Field emission scanning electron microscopy (FESEM). The phase and chemical state of the modified electrode was investigated using X-ray diffractometer (XRD) and X-ray photoelectron spectroscopy (XPS) respectively. The enhanced electrochemical activity of NPCT electrode was established by conducting hydrogen adsorption-desorption study and electrochemical oxygen reduction studies. The performance of the electrode was investigated by employing it as anode in cerium oxidation under an applied current of 0.1 A in 11.5 M nitric acid. Post performance analysis reveals the stability of the synthesized electrode. - Highlights: • Nano Pt covered Ti with higher electrochemical activity was synthesized. • Efficiency of nano Pt coated titanium was double than polycrystalline bulk Pt. • The coating was intact post experiment in very aggressive environment of HNO3

  17. A New Process Study on Comprehensive Utilization of NOx from Nitric Acid Plant

    Institute of Scientific and Technical Information of China (English)

    Zhou Hou-zhen; Liang Hua

    2003-01-01

    Based on studies of controlling NOx from nitric acid exhaust gas domestic and abroad, this paper has developed a new technique on removal of NOx and production of a by-product with high added value-- MnO2. Experiment shows, pyrolusite, whose valid composition is MnO2, of absorbing NOx has the following characteristics: quick, low cost, no secondary pollutant. Moreover, exhaust gas can attain the required standards. If the temperature of the pyrolusite serum is 30℃, pH=4, containing 90 g/L MnO2, the absorptivity for 3 000 mg/m3 NOx is 89.2%. Furthermore,few of the impurities in pyrolusite dissolve in the absorption mother solution. The purification cost of product is very low.The purity of end product MnO2 is more than 99. 995% after purifying. Therefore, it is workable for the new technique on economy and technology. There are also obvious environmental benefits and marked economic returns.

  18. Formation and electrical characteristics of silicon dioxide layers by use of nitric acid oxidation method

    International Nuclear Information System (INIS)

    SiO2/Si structure can be formed at low temperatures by use of nitric acid (HNO3) oxidation of Si (NAOS) method. When Si wafers are immersed in ∼ 40 wt% HNO3 solutions at 108 deg C, ∼ 1 nm SiO2 layers are formed. The subsequent immersion in 68 wt% HNO3 (i.e., azeotropic mixture of HNO3 with water) at 121 deg C increases the SiO2 thickness. The 3,5 nm-thick SiO2 layers produced by this two-step NAOS method possess a considerably low leakage current density (e.g. 1 x 102 A/cmi2 at the forward gate bias, VG, of 1.5 V), in spite of the low temperature oxidation, and further decreased (e.g., 8 x 104 A/cm2 at VG = 1.5 V) by post-metallization annealing at 250 deg C in hydrogen atmosphere. In order to increase the SiO2 thickness, a bias voltage is applied during the NAOS method. When 10 V is applied to Si with respect to a Pt counter electrode both immersed in 1 M HNO3 solutions at 25 deg C, SiO2 layers with 8 nm thickness can be formed for 1 h(Authors)

  19. Investigation of sorption of palladium, ruthenium and rhodium ions from nitric acid solutions sorbents of different sorts

    International Nuclear Information System (INIS)

    Data are obtained on the Pd, Ru and Rh platinum metal ion sorption from nitric acid solutions on ion-exchange resins and nonorganic sorbents of different classes. It is determined that the sorbent capacity in relation to palladium is 1-2 orders higher of corresponding capacities in relation to ruthenium and rhodium. Series of sorption ability of sorbents are determined in relation to ions of considered elements in 3 mol/l HNO3

  20. AtNOA1 modulates nitric oxide accumulation and stomatal closure induced by salicylic acid in Arabidopsis

    OpenAIRE

    Sun, Li Rong; Hao, Fu Shun; Lu, Bao Shi; Ma, Li Ya

    2010-01-01

    Phytohormone salicylic acid (SA) has been documented to induce nitric oxide (NO) generation and stomatal closure in plants. However, the cellular components mediating these processes are limited. Here, we report that NO synthesis in guard cells and stomatal closure are markedly induced by SA in Arabidopsis wild type plants, whereas these effects caused by SA are suppressed significantly in noa1 T-DNA mutant plants. These results suggest that AtNOA1 regulates SA-triggered NO accumulation and s...

  1. Effect of temperature on strontium extraction from nitric acid medium using crown ether - aliphatic alcohol as the organic solvent

    International Nuclear Information System (INIS)

    The extraction of Sr(II) from 4.0 M nitric acid was carried out employing dicyclohexano 18 crown 6 (DCH18C6) in octanol and its mixtures with butanol at varying temperature. The thermodynamic parameter ΔH was computed from the Van't Hoff plot and ΔS and ΔG values were calculated. An interesting trend was observed in the enthalpy and entropy changes with varying diluent concentration. (author)

  2. Co-Mn-Al Spinel Catalyst for Removal of N2O from Nitric Acid Plant Tail Gases

    Czech Academy of Sciences Publication Activity Database

    Obalová, L.; Karásková, K.; Kovanda, F.; Jirátová, Květa; Šrámek, J.; Kustrowski, P.; Chromčáková, Ž.; Kočí, K.; Borovec, K.; Dej, M.

    Prague : Heyrovsky Institut of Physical Chemistry of the ASCR, v. v .i, 2013 - (Žilková, N.; Horáček, M.), Po17 ISBN 978-80-87351-27-7. [Symposium on Catalysis /45./. Prague (CZ), 04.11.2013-06.11.2013] Institutional support: RVO:67985858 Keywords : Co-Mn-Al mixed oxide * nitric acid plant * catalysts Subject RIV: CI - Industrial Chemistry, Chemical Engineering http://www.jh-inst.cas.cz/~catsymp/

  3. Determination of Copper-Based Fungicides by Flame Atomic Absorption Spectrometry Using Digestion Procedure with Sulfuric and Nitric Acid

    OpenAIRE

    Jelena Milinović; Rada Đurović

    2007-01-01

    Copper-based fungicides can be effectively digested by treatment with a mixture of concentrated sulfuric and nitric acid in exactly 15 minutes for the rapid determination via copper using flame atomic absorption spectrometry (AAS). Under optimum conditions, the results of copper fungicide analysis were consistent to those obtained by the AOAC’s recommended method. Recovery values ranged from 98.63 to 103.40%. Relative standard deviation values are lower than 2%. The proposed digestion procedu...

  4. Thermal And Spectroscopic Analyses Of Next Generation Caustic Side Solvent Extraction Solvent Contacted With 3, 8, And 16 Molar Nitric Acid

    Energy Technology Data Exchange (ETDEWEB)

    Fondeur, F. F.; Fink, S. D.

    2011-12-07

    A new solvent system referred to as Next Generation Solvent or NGS, has been developed at Oak Ridge National Laboratory for the removal of cesium from alkaline solutions in the Caustic Side Solvent Extraction process. The NGS is proposed for deployment at MCU{sup a} and at the Salt Waste Processing Facility. This work investigated the chemical compatibility between NGS and 16 M, 8 M, and 3 M nitric acid from contact that may occur in handling of analytical samples from MCU or, for 3 M acid, which may occur during contactor cleaning operations at MCU. This work shows that reactions occurred between NGS components and the high molarity nitric acid. Reaction rates are much faster in 8 M and 16 M nitric acid than in 3 M nitric acid. In the case of 16 M and 8 M nitric acid, the nitric acid reacts with the extractant to produce initially organo-nitrate species. The reaction also releases soluble fluorinated alcohols such as tetrafluoropropanol. With longer contact time, the modifier reacts to produce a tarry substance with evolved gases (NO{sub x} and possibly CO). Calorimetric analysis of the reaction product mixtures revealed that the organo-nitrates reaction products are not explosive and will not deflagrate.

  5. Thermal And Spectroscopic Analyses Of Next Generation Caustic Side Solvent Extraction Solvent Contacted With 3, 8, And 16 Molar Nitric Acid

    International Nuclear Information System (INIS)

    A new solvent system referred to as Next Generation Solvent or NGS, has been developed at Oak Ridge National Laboratory for the removal of cesium from alkaline solutions in the Caustic Side Solvent Extraction process. The NGS is proposed for deployment at MCUa and at the Salt Waste Processing Facility. This work investigated the chemical compatibility between NGS and 16 M, 8 M, and 3 M nitric acid from contact that may occur in handling of analytical samples from MCU or, for 3 M acid, which may occur during contactor cleaning operations at MCU. This work shows that reactions occurred between NGS components and the high molarity nitric acid. Reaction rates are much faster in 8 M and 16 M nitric acid than in 3 M nitric acid. In the case of 16 M and 8 M nitric acid, the nitric acid reacts with the extractant to produce initially organo-nitrate species. The reaction also releases soluble fluorinated alcohols such as tetrafluoropropanol. With longer contact time, the modifier reacts to produce a tarry substance with evolved gases (NOx and possibly CO). Calorimetric analysis of the reaction product mixtures revealed that the organo-nitrates reaction products are not explosive and will not deflagrate

  6. Thermal And Spectroscopic Analyses Of Next Generation Caustic Side Solvent Extraction Solvent Contacted With 3, 8, And 16 Molar Nitric Acid

    International Nuclear Information System (INIS)

    A new solvent system referred to as Next Generation Solvent or NGS, has been developed at Oak Ridge National Laboratory for the removal of cesium from alkaline solutions in the Caustic Side Solvent Extraction process. NGS is proposed for deployment at MCU and at the Salt Waste Processing Facility. This work investigated the chemical compatibility between NGS and 16 M, 8 M, and 3 M nitric acid from contact that may occur in handling of analytical samples from MCU or, for 3 M acid, which may occur during contactor cleaning operations at MCU. This work shows that reactions occurred between NGS components and the high molarity nitric acid. In the case of 16 M and 8 M nitric acid, initially organo-nitrate groups are generated and attach to the modifier and that with time oxidation reactions convert the modifier into a tarry substance with gases (NOx and possibly CO) evolving. Calorimetric analysis of the organonitrate revealed the reaction products are not explosive nor will they deflagrate. NGS exposure to 3 M nitric acid resulted in much slower reaction kinetics and that the generated products were not energetic. We recommended conducting Accelerated Rate calorimetry on the materials generated in the 16 M and 8 M nitric acid test. Also, we recommend continue monitoring of the samples contacting NGS with 3 M nitric acid.

  7. Sorption of uranyl and thorium(IV) ions by dodecavanadium acid from diluted nitric acid solutions

    International Nuclear Information System (INIS)

    Sorption of uranyl by dodecavanadium acid (DDVA) proceeds according to ion exchange mechanism in the region of relatively low values of its concentration - (0.8-2.0) x 10-3 mol/l. Th(IV) sorption practically not depends on solution pH value in interval of pH 1.5-2.5 and changes significantly in dependence on its initial concentration. Maximal values of DDVA capacity differ for Th(IV) and UO22+ (9 and 6.3 mg-equi/g) respectively. X-ray phase analysis establishes the composition of uranyl compounds obtained during DDVA contact with concentrated solutions of uranyl nitrate that is UO2(VO3)2·nH2O

  8. Effects of boiling on chlorogenic acid and the liver protective effects of its main products against CCl₄-induced toxicity in vitro.

    Science.gov (United States)

    Kan, Shidong; Cheung, Matt Wan Man; Zhou, Yanling; Ho, Wing Shing

    2014-02-01

    Chlorogenic acid (3-O-caffeoylquinic acid, CA) is the active component in several botanical beverage, vegetables, fruits, and herbal drugs. The effect of water boiling on the bioactivity of CA was studied. CA could be isomerized to 4-O-caffeoylquinic acid (4-O-CA) and 5-O-caffeoylquinic acid (5-O-CA) in decoctive extraction, and each of the isomers occupied about one-third of the total caffeoylquinic acids. A novel method, using water elution of microsphere resin, was used to purify CA and its 2 isomers. The yield of CA, 4-O-CA, and 5-O-CA was 82%, 5.6%, and 50%, with the purity of 98%, 97%, and 99%, respectively. The DPPH radical scavenging assay showed that 4-O-CA, 5-O-CA, and CA exhibited similar activity. However, there was no significant difference between 4-O-CA and 5-O-CA when used against CCl₄-induced toxicity in hepG2 cells. Our studies show that isomerization is the main transformation of CA in boiling, and the decoction could not decrease the anti-oxidant activity of CA. PMID:24456346

  9. Effects of cold work, sensitization treatment and its combination on corrosion behavior of stainless steels in nitric acid

    International Nuclear Information System (INIS)

    In the Purex reprocessing process, the spent nuclear fuels from light water reactors are dissolved in nitric acid to separate and recover the fissile materials such as Uranium and Plutonium from the radioactive fission products. To ensure safety and reliable operation of the reprocessing plant, superior corrosion resistance is required to the structural materials of the plant, and stainless steels have been used as one of the main structural materials because of its very good performance in a nitric acid environment. Corrosion behavior of stainless steels was investigated in nitric acid for the effect of cold work, sensitization heat treatment and its combination. Corrosion rate of solution-treated Type 304 with extra low carbon (304 ELC) increased with time and reached constant values after 1,000 h of immersion time. Constant corrosion rates, however, were obtained for 25Cr-20Ni-Nb (310 Nb) from the initial stage of immersion. Cold work mitigated corrosion of the solution-treated stainless steels. The effect of cold work was different on the two stainless steels with sensitization heat treatment, showing accelerated corrosion for 304 ELC. The corrosion resistance of 310 Nb was superior to 304ELC after all the treatments. Chromium concentration of the sensitization treated 304 ELC was lower in the grain-boundary region than that of the solution-treated one, although no chromium carbide precipitation was observed. This might be the cause of corrosion enhancement by sensitization treatment

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

    International Nuclear Information System (INIS)

    Upper East Fork Poplar Creek OU-2 consists of the Abandoned Nitric Acid Pipeline. This pipeline was installed in 1951 to transport liquid wastes ∼ 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

  11. Study on reduction and back extraction of Pu(IV) by urea derivatives in nitric acid conditions

    International Nuclear Information System (INIS)

    The reduction kinetics of Pu(IV) by hydroxyl-semicarbazide (HSC), hydroxyurea (HU) and di-hydroxyurea (DHU) in nitric acid solutions were investigated separately with adequate kinetic equations. In addition, counter-current cascade experiments were conducted for Pu split from U in nitric acid media using three kinds of reductant, respectively. The results show that urea derivatives as a kind of novel salt-free reductant can reduce Pu(IV) to Pu(III) rapidly in the nitric acid solutions. The stripping experimental results showed that Pu(IV) in the organic phase can be stripped rapidly to the aqueous phase by the urea derivatives, and the separation factors of plutonium /uranium can reach more than 104. This indicates that urea derivatives is a kind of promising salt-free agent for uranium/plutonium separation. In addition, the complexing effect of HSC with Np(IV) was revealed, and Np(IV) can be back-extracted by HSC with a separation factor of about 20

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

    Energy Technology Data Exchange (ETDEWEB)

    1993-12-01

    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.

  13. Nitric acid in the stratosphere based on Odin observations from 2001 to 2007 – Part 1: A global climatology

    Directory of Open Access Journals (Sweden)

    M. L. Santee

    2008-05-01

    Full Text Available The Sub-Millimetre Radiometer (SMR on board the Odin satellite, launched in February 2001, observes thermal emissions of stratospheric nitric acid (HNO3 originating from the Earth limb in a band centred at 544.6 GHz. Height-resolved measurements of the global distribution of nitric acid in the stratosphere between ~18–45 km (~1.5–60 hPa were performed approximately on two observation days per week. An HNO3 climatology based on roughly 6 years of observations from August 2001 to December 2007 was created. The study highlights the spatial and seasonal variation of nitric acid in the stratosphere, characterised by a pronounced seasonal cycle at middle and high latitudes with maxima during late fall and minima during spring, strong denitrification in the lower stratosphere of the Antarctic polar vortex during winter (the irreversible removal of NOy by the sedimentation of cloud particles containing HNO3, as well as high quantities of HNO3 formed every winter at high-latitudes in the middle and upper stratosphere. A strong inter-annual variability is observed in particular at high latitudes. A comparison with a stratospheric HNO3 climatology based on UARS/MLS measurements from the 1990s shows a good consistency and agreement of the main morphological features in the potential temperature range ~465 to ~960 K, if the different characteristics of the data sets such as altitude range and resolution are considered.

  14. Development of a Quantum Cascade Laser-Based Detector for Ammonia and Nitric Acid

    Energy Technology Data Exchange (ETDEWEB)

    Zahniser, Mark S.; Nelson, David D.; McManus, J. Barry; Shorter, Joanne H.; Herndon, Scott C.; Jimenez, Rodrigo

    2005-12-31

    We have developed a compact, robust, atmospheric trace gas detector based on mid-infrared absorption spectroscopy using pulsed quantum cascade (QC) lasers. The spectrometer is suitable for airborne measurements of ammonia, nitric acid, formaldehyde, formic acid, methane, nitrous oxide, carbon monoxide, nitrogen dioxide and other gases that have line-resolved absorption spectra in the mid-infrared spectral region. The QC laser light source operates near room temperature with thermal electric cooling instead of liquid nitrogen which has been previously required for semiconductor lasers in the mid-infrared spectral region. The QC lasers have sufficient output power so that thermal electric cooled detectors may be used in many applications with lower precision requirements. The instrument developed in this program has been used in several field campaigns from both the Aerodyne Mobile Laboratory and from the NOAA WP3 aircraft. The Phase II program has resulted in more than 10 archival publications describing the technology and its applications. Over 12 instruments based on this design have been sold to research groups in Europe and the United States making the program both a commercial as well as a technological success. Anticipated Benefits The development of a sensitive, cryogen-free, mid-infrared absorption method for atmospheric trace gas detection will have wide benefits for atmospheric and environmental research and broader potential commercial applications in areas such as medical diagnostic and industrial process monitoring of gaseous compounds. Examples include air pollution monitoring, breath analysis, combustion exhaust diagnostics, and plasma diagnostics for semi-conductor fabrication. The substitution of near-room temperature QC lasers for cryogenic lead salt TDLs and the resulting simplifications in instrument design and operation will greatly expand the range of applications.

  15. Oscillate Boiling

    CERN Document Server

    Li, Fenfang; Nguyen, Dang Minh; Ohl, Claus-Dieter

    2016-01-01

    We report about an intriguing boiling regime occurring for small heaters embedded on the boundary in subcooled water. The microheater is realized by focusing a continuous wave laser beam to about $10\\,\\mu$m in diameter onto a 165\\,nm-thick layer of gold, which is submerged in water. After an initial vaporous explosion a single bubble oscillates continuously and repeatably at several $100\\,$kHz. The microbubble's oscillations are accompanied with bubble pinch-off leading to a stream of gaseous bubbles into the subcooled water. The self-driven bubble oscillation is explained with a thermally kicked oscillator caused by the non-spherical collapses and by surface pinning. Additionally, Marangoni stresses induce a recirculating streaming flow which transports cold liquid towards the microheater reducing diffusion of heat along the substrate and therefore stabilizing the phenomenon to many million cycles. We speculate that this oscillate boiling regime may allow to overcome the heat transfer thresholds observed dur...

  16. Extraction of lanthanide(III) and uranyl(VI) from nitric acid solution by N,N'-dimethyl-N,N'-dibutylmalonamide

    International Nuclear Information System (INIS)

    The extractive properties of N,N'-dimethyl-N,N'-dibutylmalonamide (DMDBMA) and the loading capacity of extraction solvents containing DMDBMA for lanthanide(III) and uranyl(VI) ions in nitric acid solution were investigated. The dependence of the distribution ratio on the concentration of nitric acid shows that DMDBMA has an ability to extract uranyl(VI) ions, while the extracting capacity for lanthanide(III) ions is not enough for the application in practice. 17 refs., 10 figs., 4 tabs

  17. Fast and Simultaneous Determination of Pu(Ⅳ) and Nitric Acid in Spent Nuclear Fuel Reprocessing Sample by Near Infrared Spectroscopy

    Institute of Scientific and Technical Information of China (English)

    LI; Ding-ming; ZHANG; Li-hua; WANG; Ling; GONG; Yan-ping; FAN; De-jun; YI; Bao-shan; CHEN; Qiang; JI; Yong-chao; WU; Ji-zong

    2013-01-01

    Determination of Pu(Ⅳ)and nitric acid plays significant role in nuclear fuel reprocessing plant to control process accurately and timely.Coupling C-T fixed-type grating with InGaAs detector,a new novel analytical system for simultaneous measurement of nitric acid and Pu(Ⅳ)was developed by our working group.After obtaining near infrared absorptive spectra by the spectroscopic instrument,the spectra data

  18. Comparing the effects of inorganic nitrate and allopurinol in renovascular complications of metabolic syndrome in rats: role of nitric oxide and uric acid

    OpenAIRE

    Essawy, Soha S.; Abdel-Sater, Khaled A.; Elbaz, Amani A.

    2013-01-01

    Introduction The epidemic of metabolic syndrome is increasing worldwide and correlates with elevation in serum uric acid and marked increase in total fructose intake. Fructose raises uric acid and the latter inhibits nitric oxide bioavailability. We hypothesized that fructose-induced hyperuricemia may have a pathogenic role in metabolic syndrome and treatment of hyperuricemia or increased nitric oxide may improve it. Material and methods Two experiments were performed. Male Sprague-Dawley rat...

  19. Low Temperature Selective Catalytic Reduction of Nitrogen Oxides in Production of Nitric Acid by the Use of Liquid

    Directory of Open Access Journals (Sweden)

    Kabljanac, Ž.

    2011-11-01

    Full Text Available This paper presents the application of low-temperature selective catalytic reduction of nitrous oxides in the tail gas of the dual-pressure process of nitric acid production. The process of selective catalytic reduction is carried out using the TiO2/WO3 heterogeneous catalyst applied on a ceramic honeycomb structure with a high geometric surface area per volume. The process design parameters for nitric acid production by the dual-pressure procedure in a capacity range from 75 to 100 % in comparison with designed capacity for one production line is shown in the Table 1. Shown is the effectiveness of selective catalytic reduction in the temperature range of the tail gas from 180 to 230 °C with direct application of liquid ammonia, without prior evaporation to gaseous state. The results of inlet and outlet concentrations of nitrous oxides in the tail gas of the nitric acid production process are shown in Figures 1 and 2. Figure 3 shows the temperature dependence of the selective catalytic reduction of nitrous oxides expressed as NO2in the tail gas of nitric acid production with the application of a constant mass flow of liquid ammonia of 13,0 kg h-1 and average inlet mass concentration of the nitrous oxides expressed as NO2of 800,0 mgm-3 during 100 % production capacity. The specially designed liquid-ammonia direct-dosing system along with the effective homogenization of the tail gas resulted in emission levels of nitrous oxides expressed as NO2 in tail gas ranging from 100,0 to 185,0 mg m-3. The applied low-temperature selective catalytic reduction of the nitrous oxides in the tail gases by direct use of liquid ammonia is shown in Figure 4. It is shown that low-temperature selective catalytic reduction with direct application of liquid ammonia opens a new opportunity in the reduction of nitrous oxide emissions during nitric acid production without the risk of dangerous ammonium nitrate occurring in the process of subsequent energy utilization of

  20. Biochemistry of Nitric Oxide

    OpenAIRE

    Habib, Safia; Ali, Asif

    2011-01-01

    Nitric oxide (NO) a free radical having both cytoprotective as well as tumor promoting agent is formed from l-arginine by converting it to l-citrulline via nitric oxide synthase enzymes. The reaction product of nitric oxide with superoxide generates potent oxidizing agent, peroxynitrite which is the main mediator of tissue and cellular injury. Peroxynitrite is reactive towards many biomolecules which includes amino acids, nucleic acid bases; metal containing compounds, etc. NO metabolites may...

  1. Selective extraction of plutonium from nitric acid medium by bifunctional polyethersulfone beads for quantification with thermal ionisation mass spectrometry

    International Nuclear Information System (INIS)

    Polyethersulfone (PES) magnetic beads were prepared by phase inversion technique. The beads were grafted with two monomers, viz. 2-hydroxyethylmethacrylate phosphoric acid (HEMP) and (3-acrylamidopropyl)trimethyl ammonium chloride (AMAC), by photo-induced free radical polymerization. Effect of different HNO3 concentrations on the sorption profiles of Am(III) and Pu(IV) was studied using the grafted PES beads. The beads were found to extract plutonium quantitatively from high nitric acid medium (3-8 M). The effect of presence of competing actinide, e.g. U(VI), on the sorption of Pu(IV) was also studied. (author)

  2. Dissolution Of Plutonium Metal Using Nitric Acid Solutions Containing Potassium Fluoride

    International Nuclear Information System (INIS)

    The deinventory and deactivation of the Savannah River Site's (SRS's) FB-Line facility required the disposition of approximately 2000 items from the facility's vaults. Plutonium (Pu) scraps and residues which do not meet criteria for conversion to a mixed oxide fuel will be dissolved and the solution stored for subsequent disposition. Some of the items scheduled for dissolution are composite materials containing Pu and tantalum (Ta) metals. The preferred approach for handling this material is to dissolve the Pu metal, rinse the Ta metal with water to remove residual acid, and burn the Ta metal. The use of a 4 M nitric acid (HNO3) solution containing 0.2 M potassium fluoride (KF) was initially recommended for the dissolution of approximately 500 g of Pu metal. However, prior to the use of the flowsheet in the SRS facility, a new processing plan was proposed in which the feed to the dissolver could contain up to 1250 g of Pu metal. To evaluate the use of a larger batch size and subsequent issues associated with the precipitation of plutonium-containing solids from the dissolving solution, scaled experiments were performed using Pu metal and samples of the composite material. In the initial experiment, incomplete dissolution of a Pu metal sample demonstrated that a 1250 g batch size was not feasible in the HB-Line dissolver. Approximately 45% of the Pu was solubilized in 4 h. The remaining Pu metal was converted to plutonium oxide (PuO2). Based on this work, the dissolution of 500 g of Pu metal using a 4-6 h cycle time was recommended for the HB-Line facility. Three dissolution experiments were subsequently performed using samples of the Pu/Ta composite material to demonstrate conditions which reduced the risk of precipitating a double fluoride salt containing Pu and K from the dissolving solution. In these experiments, the KF concentration was reduced from 0.2 M to either 0.15 or 0.175 M. With the use of 4 M HNO3 and a reduction in the KF concentration to 0.175 M

  3. Inhibitory effects of indole α-lipoic acid derivatives on nitric oxide production in LPS/IFNγ activated RAW 264.7 macrophages.

    Science.gov (United States)

    Karabay, Arzu Zeynep; Koc, Aslı; Gurkan-Alp, A Selen; Buyukbingol, Zeliha; Buyukbingol, Erdem

    2015-04-01

    Alpha-lipoic acid (α-lipoic acid) is a potent antioxidant compound that has been shown to possess anti-inflammatory effects. RAW 264.7 macrophages produce various inflammatory mediators such as nitric oxide, IL-1β, IL-6 and TNF-alpha upon activation with LPS (Lipopolysaccharide) and IFNγ (interferon gamma). In this study, the effect of 12 synthetic indole α-lipoic acid derivatives on nitric oxide production and iNOS (inducible nitric oxide synthase) protein expression in LPS/IFNγ activated RAW 264.7 macrophages was determined. Cell proliferation, nitric oxide levels and iNOS protein expression were examined with thiazolyl blue tetrazolium blue test, griess assay and western blot, respectively. Our results showed that all of the indole α-lipoic acid derivatives showed significant inhibitory effects on nitric oxide production and iNOS protein levels (p < 0.05). The most active compounds were identified as compound I-4b, I-4e and II-3b. In conclusion, these indole α-lipoic acid derivatives may have the potential for treatment of inflammatory conditions related with high nitric oxide production. PMID:25727912

  4. Potentiality of uranium biosorption from nitric acid solutions using shrimp shells

    International Nuclear Information System (INIS)

    Biosorption has gained important credibility during recent years because of its good performance and low cost. This work is concerned with studying the potentiality of the chitin component of the shrimp shells for uranium biosorption from nitric acid liquid solutions. The structural characteristics of the working chitin have been determined via Fourier Transform Infrared Spectroscopy (FTIR). The surface morphology was examined using Scanning Electron Microscopy (SEM). The adsorption capacity of biomass was investigated experimentally. The influence of contact time, pH, metal ion concentration, solution volume to mass ratio and temperature were evaluated and the results were fitted using adsorption isotherm models. The kinetic of uranium biosorption was also investigated as well as biosorption thermodynamic. - Graphical abstract: Physicochemical process of biosorption is known to be promising technique due to the ease of operation and comparable low cost of biosorbant application. Chitin flakes extracted from shrimp shells show potentiality in uranium adsorption reached 7.48 mg uranium at the following conditions: 60 min contact time, pH 3.66, 50:1 V/m ration and at room temperature. The theoretical sorption capacity was 25.31 mg g−1, according to Langmuir isotherm model. The rate of sorption follows pseudo second-order. The nature of biosorption process is spontaneous and exothermic. - Highlights: • This study shows the potentially for shrimp shell beads for uranium adsorption. • The max. biosorption was achieved at pH 3.6, contact time 60 min, S/L ratio 1:50. • Uranium sorption follows Langmuir isotherm with theoretical capacity of 25.31 g/kg. • The nature of sorption process of the sorbents is spontaneous and exothermic. • The rate of sorption follows pseudo second-order

  5. Rocket Performance of Red Fuming Nitric Acid with Blends of Norbornadiene, Carene and Cardanol

    Directory of Open Access Journals (Sweden)

    R. Chhibber

    1992-07-01

    Full Text Available The fuel blends of nornornadiene and carene (50:50 by weight and norbornadiene, carene and cardanol (40:40:20 by weight exhibit synergistic hypergolic ignition with red fuming nitric acid (RFNA as oxidiser. These fuel blends have been evaluated by theoretical calculations of performance parameters and subsequently verified by static firing in a 10 kg/sub f/ thruster at a chamber pressure of around 20 atm, using RFNA (with 21 per cent N/sub 2/O/sub 4/ by weight as oxidiser. The theoretical calculations show maximum specific impulse and C*values at the O/F, 3 to be 227.8 s and 1598.7 m/s respectively for the norbornadiene-carene blend. The corresponding values for the norbornadiene, carene and cardanol blend were found to be 226.8 s and 1586.0 m/s respectively at the O/F, 4. For theoretical calculations, the chamber pressure (P/sub c and the exit pressure (P/sub e/0 were assumed to be 20 and 1 atm, respectively. The static firing of the propellants in a 10 kg thruster exhibited smooth pressure-time curves with the experimental C* values in close agreement with those calculated and the non-deposition of carbon in the nozzle. This indicated low combustion instability and high combustion efficiency under rocket conditions (> 0.9. The fuel blends with their low cost and toxicity and relatively high density can replace G-fuel used in several Indian missiles without impairing the performance.

  6. Photochemical mutual separation technology between plutonium and neptunium in nitric acid solution

    International Nuclear Information System (INIS)

    A photochemical method of removing Np from a mixture of nitric acid solutions of Pu and Np has been studied in connection with the Purex reprocessing procedure. The valencies and concentrations of Pu and Np in the initial samples were adjusted to Pu(III) and Np(V) and to 1x10-4 or 1x10-3 M (M=mol.dm-3), respectively. Experiments were carried out under various conditions by varying the irradiation rates of the Hg lamp and concentrations of HNO3. Under the conditions of an irradiation rate of 0.015 Watt (W), a 3 N HNO3 solution containing reductants and a Pu concentration of 1x10-4 M, the initial valence of Pu(III) was rapidly oxidized to Pu(IV), and more than 95% of Pu(IV) remained at the same valence even after continuous irradiation. On the other hand, Np(V) did not change. These valences, Pu(III) and Np(V), are optimum for separating Np from Pu using TBP-n-dodecane extraction. These results lead to the conclusion that the photochemical valence adjustment has a high potential for removing Np from a Pu and Np mixed solution and for re-oxidation process technology instead of the conventional process using NOx gas. Furthermore, the photochemical reaction mechanism of Pu and Np was discussed from the standpoint of thermodynamic considerations, and then the applicability of this photochemical technology in a reprocessing process was discussed based on the experimental data obtained in this work. (orig.)

  7. Reactions of Am(III) and Eu(III) with potassium ferricyanide in nitric acid solutions

    International Nuclear Information System (INIS)

    The reactions between Am or Eu present in 0.1 M nitric acid solutions, alone or both together, with 0.25 M K3Fe(CN)6, were studied at room temperature. When Am was the only trivalent metal ion in solution, precipitation of AmFe(CN)6 occurs and the residual Am concentration is about equal to 0.95 mM. However, when Am initial concentration is less than the above specified value for AmFe(CN)6 solubility, Am residual concentration measured is lower that its concentration in the initial solutions. The solubility of EuFe(CN)6 was found to be equal to 30 mM. However, when precipitate formation occurs, the Eu residual concentration after phase separation is about in average 8 mM. When Am and Eu were simultaneously present at the same concentration in solution, the solubility of Am differs little from that measured with Am alone. For initial Am concentrations below 1 mM, the solubility of Am is higher than that observed in the absence of Eu. For initial concentrations of about 8 mM, the Am solubility is lower (about 0.7 mM) than that observed for Am alone. When the initial Eu concentration is constant at 29 mM, the Am precipitation efficiency is much higher than observed in the absence of Eu, for Am concentrations between 30 and 0.5 mM. The residual Am concentratixon in solution thus drops considerably in the presence of Eu (29 mM), and is about 0.04 mM for initial Am concentrations below 4 mM

  8. Intergranular corrosion testing of austenitic stainless steels in nitric acid solutions

    Energy Technology Data Exchange (ETDEWEB)

    Whillock, G.O.H.; Dunnett, B. F. [British Nuclear Fuels plc, BNFL, B170, Sellafield, Seascale, Cumbria CA20 1PG (United Kingdom)

    2004-07-01

    In hot strong nitric acid solutions, stainless steels exhibit intergranular corrosion. Corrosion rates are often measured from immersion testing of specimens manufactured from the relevant material (e.g. plate or pipe). The corrosion rates, measured from weight loss, are found to increase with time prior to reaching steady state, which can take thousands of hours to achieve. The apparent increase in corrosion rate as a function of time was found to be an artefact due to the surface area of the specimen's being used in the corrosion rate calculations, rather than that of the true area undergoing active corrosion i.e. the grain boundaries. The steady state corrosion rate coincided with the onset of stable grain dropping, where the use of the surface area of the specimen to convert the weight loss measurements to corrosion rates was found to be appropriate. This was confirmed by sectioning of the specimens and measuring the penetration depths. The rate of penetration was found to be independent of time and no induction period was observed. A method was developed to shorten considerably the testing time to reach the steady state corrosion rate by use of a pre-treatment that induces grain dropping. The long-term corrosion rates from specimens which were pre-treated was similar to that achieved after prolonged testing of untreated (i.e. initially ground) specimens. The presence of cut surfaces is generally unavoidable in the simple immersion testing of specimens in test solutions. However, inaccuracy in the results may occur as the measured corrosion rate is often influenced by the orientation of the microstructure, the highest rates typically being observed on the cut surfaces. Two methods are presented which allow deconvolution of the corrosion rates from immersion testing of specimens containing cut surfaces, thus allowing reliable prediction of the long-term corrosion rate of plate surfaces. (authors)

  9. Intergranular corrosion testing of austenitic stainless steels in nitric acid solutions

    International Nuclear Information System (INIS)

    In hot strong nitric acid solutions, stainless steels exhibit intergranular corrosion. Corrosion rates are often measured from immersion testing of specimens manufactured from the relevant material (e.g. plate or pipe). The corrosion rates, measured from weight loss, are found to increase with time prior to reaching steady state, which can take thousands of hours to achieve. The apparent increase in corrosion rate as a function of time was found to be an artefact due to the surface area of the specimen's being used in the corrosion rate calculations, rather than that of the true area undergoing active corrosion i.e. the grain boundaries. The steady state corrosion rate coincided with the onset of stable grain dropping, where the use of the surface area of the specimen to convert the weight loss measurements to corrosion rates was found to be appropriate. This was confirmed by sectioning of the specimens and measuring the penetration depths. The rate of penetration was found to be independent of time and no induction period was observed. A method was developed to shorten considerably the testing time to reach the steady state corrosion rate by use of a pre-treatment that induces grain dropping. The long-term corrosion rates from specimens which were pre-treated was similar to that achieved after prolonged testing of untreated (i.e. initially ground) specimens. The presence of cut surfaces is generally unavoidable in the simple immersion testing of specimens in test solutions. However, inaccuracy in the results may occur as the measured corrosion rate is often influenced by the orientation of the microstructure, the highest rates typically being observed on the cut surfaces. Two methods are presented which allow deconvolution of the corrosion rates from immersion testing of specimens containing cut surfaces, thus allowing reliable prediction of the long-term corrosion rate of plate surfaces. (authors)

  10. Contribution to the study of the redox couple Np(VI)/Np(V) in the presence of uranium(VI) in solutions of nitric acid and nitrous acid

    International Nuclear Information System (INIS)

    The redox behavior of the Np(VI)/Np(V) couple was the subject of a spectrometric study of the Np(VI) reduction reaction in nitric acid solutions (4 to 5 M) containing variable concentrations (1.5 to 3.5 x 10-3 M) of nitrous acid. A low nitrous acid concentration and a high nitric acid concentration were found to favor the stabilization of Np(VI). The stoichiometric coefficients of nitrous acid and nitric acid in the Np(VI) reduction reaction were determined thermodynamically, although only the reaction order with respect to HNO2 could be calculated from a kinetic analysis. Adding nitrate ions to a HNO3/HNO2 solution enhanced the stability of neptunium at oxidation state +VI, but also increased the reduction rate. When uranium(VI) was added to the HNO3/HNO2 solutions, the total quantity of neptunium at oxidation state +V (either free or as a Np(V)-U(VI) complex) remained practically unchanged, as did the Np(VI) reduction rate. The electrochemical behavior of the Np(VI)/Np(V) couple was investigated in a weak acidic medium by voltammetry with an ultra-micro-electrode (UME). The oxidation wave limiting current variation was a linear function of the Np(V) concentration when a gold UME was used, but not with a platinum UME; the reduction wave limiting current variation versus the Np(V) concentration was linear with either gold or platinum UMEs. The presence of the Np(V)-U(VI) complex in the neptunium solutions was characterized by a shift in the normal apparent potential of the Np(VI)/Np(V) couple toward anodic potentials consistent with the previously determined values of the complexation constants. (author)

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

    International Nuclear Information System (INIS)

    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 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

  12. Involvement of Nitric Oxide on Calcium Mobilization and Arachidonic Acid Pathway Activation during Platelet Aggregation with different aggregating agonists.

    Science.gov (United States)

    Banerjee, Debipriya; Mazumder, Sahana; Kumar Sinha, Asru

    2016-03-01

    Platelet aggregation by different aggregating agonists is essential in the normal blood coagulation process, the excess of which caused acute coronary syndrome (ACS). In all cases, the activation of arachidonic acid by cycloxygenase was needed for the synthesis of thromboxane A2 (TXA2) but the mechanism of arachidonic acid release in platelets remains obscure. Studies were conducted to determine the role of nitric oxide (NO), if any, on the release of arachidonic acid in platelets. The cytosolic Ca(2+) was visualized and quantitated by fluorescent spectroscopy by using QUIN-2. NO was measured by methemoglobin method. Arachidonic acid was determined by HPLC. TXA2 was measured as ThromboxaneB2 (TXB2) by ELISA. Treatment of platelets in platelet-rich plasma (PRP) with different aggregating agents resulted in the inhibition of nitric oxide synthase (NOS) which inhibited the production of NO synthesis and increased TXA2 synthesis. Furthermore, the treatment of washed PRP with different platelet aggregating agents resulted in the increase of [Ca(2+)] in nM ranges. In contrast, the pre-treatment of washed PRP with aspirin increased platelet NO level and inhibited the Ca(2+) mobilization and TXA2 synthesis. These results indicated that the aggregation of platelets by different aggregating agonists was caused by the cytosolic Ca(2+) mobilization due to the inhibition of NOS. PMID:27127451

  13. The Significance of Lewis Acid Sites for the Selective Catalytic Reduction of Nitric Oxide on Vanadium-Based Catalysts.

    Science.gov (United States)

    Marberger, Adrian; Ferri, Davide; Elsener, Martin; Kröcher, Oliver

    2016-09-19

    The long debated reaction mechanisms of the selective catalytic reduction (SCR) of nitric oxide with ammonia (NH3 ) on vanadium-based catalysts rely on the involvement of Brønsted or Lewis acid sites. This issue has been clearly elucidated using a combination of transient perturbations of the catalyst environment with operando time-resolved spectroscopy to obtain unique molecular level insights. Nitric oxide reacts predominantly with NH3 coordinated to Lewis sites on vanadia on tungsta-titania (V2 O5 -WO3 -TiO2 ), while Brønsted sites are not involved in the catalytic cycle. The Lewis site is a mono-oxo vanadyl group that reduces only in the presence of both nitric oxide and NH3 . We were also able to verify the formation of the nitrosamide (NH2 NO) intermediate, which forms in tandem with vanadium reduction, and thus the entire mechanism of SCR. Our experimental approach, demonstrated in the specific case of SCR, promises to progress the understanding of chemical reactions of technological relevance. PMID:27553251

  14. Hydrogen Peroxide and Nitric Oxide are Involved in Salicylic Acid-Induced Salvianolic Acid B Production in Salvia miltiorrhiza Cell Cultures

    OpenAIRE

    Hongbo Guo; Xiaolin Dang; Juane Dong

    2014-01-01

    Hydrogen peroxide (H2O2) and nitric oxide (NO) are key signaling molecules in cells whose levels are increased in response to various stimuli and are involved in plant secondary metabolite synthesis. In this paper, the roles of H2O2 and NO on salvianolic acid B (Sal B) production in salicylic acid (SA)-induced Salvia miltiorrhiza cell cultures were investigated. The results showed that H2O2 could be significantly elicited by SA, even though IMD (an inhibitor of NADPH oxidase) or DMTU (a quenc...

  15. Folic Acid Reverses Nitric Oxide Synthase Uncoupling and Prevents Cardiac Dysfunction in Insulin Resistance: Role of Ca2+/Calmodulin-Activated Protein Kinase II

    OpenAIRE

    Roe, Nathan D.; He, Emily Y.; Wu, Zhenbiao; Ren, Jun

    2013-01-01

    Nitric oxide synthase (NOS) may be uncoupled to produce superoxide rather than nitric oxide (NO) under pathological conditions such as diabetes mellitus and insulin resistance, leading to cardiac contractile anomalies. Nonetheless, the role of NOS uncoupling in insulin resistance-induced cardiac dysfunction remains elusive. Given that folic acid may produce beneficial effect for cardiac insufficiency partially through its NOS recoupling capacity, this study was designed to evaluate the effect...

  16. Dialkylmethyl-2-(N,N-diisobutyl)acetamidoammonium iodide as a ruthenium selective ligand from nitric acid medium

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Shikha [Bio-Organic Division, Bhabha Atomic Research Center, Trombay, Mumbai 400085 (India); Ghosh, Sunil K., E-mail: ghsunil@barc.gov.in [Bio-Organic Division, Bhabha Atomic Research Center, Trombay, Mumbai 400085 (India); Sharma, Joti N., E-mail: jnsharma@barc.gov.in [Process Development Division, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India)

    2015-09-15

    Highlights: • A new class of quart-ammonium based ligands have been designed and synthesized. • Ligand showed high extractability and selectivity for Ru in nitric acid medium. • Results are better compared to other extractants reported so far. • The iodide ion played key role in extraction process. • The composition of the extracted complex was found to be L[Ru(NO)(NO{sub 3}){sub 3}I]. - Abstract: A new class of quaternary ammonium iodide based ligands with 2-(N,N-diisobutyl)acetamide as an alkyl appendage have been designed, synthesized and tested for their ability to extract ruthenium selectively from nitric acid medium. The 2-(N,N-diisobutyl)acetamido ammonium iodide with two propyl and a methyl substituents showed best results for the recovery of ruthenium. The optimized concentration of the solvent was found to be 0.2 M in 30% isodecyl alcohol/n-dodecane. The stoichiometry of the complex was ascertained by slope analysis method and was found to be 1:1 with respect to ligand L{sup +}I{sup −} and Ru(NO)(NO{sub 3}){sub 3}. Ruthenium formed an adduct of structure LRu(NO)(NO{sub 3}){sub 3}I in the extraction medium. Iodide ion played an important role in the formation of the stable and extractable complex of ruthenium. No extraction was observed when iodide was replaced by nitrate anion in the ligand. The ligand also showed good selectivity for ruthenium in the presence of other metal ions commonly found in nitric acid solutions of nuclear waste.

  17. Dialkylmethyl-2-(N,N-diisobutyl)acetamidoammonium iodide as a ruthenium selective ligand from nitric acid medium

    International Nuclear Information System (INIS)

    Highlights: • A new class of quart-ammonium based ligands have been designed and synthesized. • Ligand showed high extractability and selectivity for Ru in nitric acid medium. • Results are better compared to other extractants reported so far. • The iodide ion played key role in extraction process. • The composition of the extracted complex was found to be L[Ru(NO)(NO3)3I]. - Abstract: A new class of quaternary ammonium iodide based ligands with 2-(N,N-diisobutyl)acetamide as an alkyl appendage have been designed, synthesized and tested for their ability to extract ruthenium selectively from nitric acid medium. The 2-(N,N-diisobutyl)acetamido ammonium iodide with two propyl and a methyl substituents showed best results for the recovery of ruthenium. The optimized concentration of the solvent was found to be 0.2 M in 30% isodecyl alcohol/n-dodecane. The stoichiometry of the complex was ascertained by slope analysis method and was found to be 1:1 with respect to ligand L+I− and Ru(NO)(NO3)3. Ruthenium formed an adduct of structure LRu(NO)(NO3)3I in the extraction medium. Iodide ion played an important role in the formation of the stable and extractable complex of ruthenium. No extraction was observed when iodide was replaced by nitrate anion in the ligand. The ligand also showed good selectivity for ruthenium in the presence of other metal ions commonly found in nitric acid solutions of nuclear waste

  18. Field test of four methods for gas-phase ambient nitric acid

    Science.gov (United States)

    Arnold, J. R.; Hartsell, Benjamin E.; Luke, Winston T.; Rahmat Ullah, S. M.; Dasgupta, Purnendu K.; Greg Huey, L.; Tate, Paul

    Three semi-continuous methods for detecting nitric acid (HNO 3) were tested against the annular denuder + filter pack (ADS) integrated collection technique at the Tampa Bay Regional Atmospheric Chemistry Experiment (BRACE) Sydney research station ˜20km downwind of the Tampa, Florida, urban core. The semi-continuous instruments included: two slightly differing implementations of the NOY-NO (total oxides of nitrogen minus that total denuded of HNO 3) denuder difference technique, one from the NOAA Air Resources Lab (ARL), and one from Atmospheric Research and Analysis, Inc. (ARA); the parallel plate wet diffusion scrubber + online ion chromatography technique from Texas Tech University (TTU); and the chemical ionization mass spectrometer from the Georgia Institute of Technology (GIT). Twelve hour ADS samples were collected by the University of South Florida (USF). Results for 10 min samples computed from the various higher sampling frequencies of each semi-continuous instrument showed good agreement (R2>0.7) for afternoon periods of the highest production and accumulation of HNO 3. Further, agreement was within ±30% for these instruments even at HNO 3 concentrations 60% for the nighttime samples; ADS results were below the corporate mean maximum HNO 3 concentration by >30% as well. The four instruments using semi-continuous methods, by contrast, were all within 10% of each other's 12 h mean mixing ratios. While only ARA employed a formal minimum detection limit at 0.050 ppb, error analysis with the other techniques established that at the same level of precision, TTU's effective limit was approximately the same as ARA's and that ARL's limit was 0.030 ppb; analysis for GIT showed no apparent effective limit at the levels of HNO 3 encountered in this field study. The importance of sample inlet height for HNO 3 measurements was indirectly shown through comparison to previous field work at this site when sample inlet heights ranged from 1.5-10 m and produced systematic

  19. Extraction of uranium(VI) in nitric acid solution with supercritical carbon dioxide fluid containing tributylphosphate

    International Nuclear Information System (INIS)

    Extraction behaviors of U(VI) and selected fission product elements from HNO3 solution into a supercritical CO2 fluid containing tributylphosphate (TBP) were studied under equilibrium and dynamic extraction conditions. Uranium(VI) was found to be extracted in the supercritical CO2 phase as a form of UO2 (NO3)2(TBP)2 with a distribution ratio of, e.g., 2.2±0.3 for the extraction of 2 x 10-4 to 2 x 10-2 M U(VI) from 3 M HNO3 into supercritical CO2-0.3 M TBP mixture at 60 C and 15 MPa. The distribution ratio of U(VI) increased with an increase of HNO3 concentration (0.1-6 M) or TBP (0.1-0.3 M), along with a decrease of pressure (10-40 MPa) at 60 C, and with an increase of the temperature (40-80 C) at 15 MPa. A salting-out effect enhancing the distribution of U(VI) was observed by addition of a fairly high concentration of LiNO3 to the aqueous phase. Results of dynamic extraction using a continuous flow of supercritical CO2-TBP through the aqueous nitric acid solution showed that >98% of U(VI) could be exctracted from 3 M HNO3 + 3 M LiNO3 solution into supercritical CO2-0.08 M TBP (60 C, 15 MPa). Main fission product elements such as lanthanides, Cs, Sr, Ba, Zr, Mo, and Pd were hardly extracted into the supercritical CO2 phase under this condition, which suggests that the supercritical CO2 extraction is a feasible method for the separation and recovery of uranium from these elements. Since rapid and complete removal of the CO2 medium from the extracts is attained by gasification of CO2, the amount of the organic solvent waste generated in the extraction process can be largely minimized. Advantages of the supercritical CO2 extraction in its application to the separation process in the field of nuclear technology are discussed. (orig.)

  20. Effect of Nitric Acid on the Low Fluorescing Performance of Drilling Fluid Lubricant Based Animal and Vegetable Oils

    Directory of Open Access Journals (Sweden)

    Feng-shan Zhou

    2013-01-01

    Full Text Available After synthesis of mixed fatty acid triethanolamine ester surfactant based on animal and vegetable mixed oils, the reaction solution was added into 4% (wt/wt liquid nitric acid or 9% (wt/wt solid nitric acid as eliminating fluorescent agent continuing to react from 1 to 2 hours. The low fluorescence lubricant named E167 for drilling fluid was prepared, in which maximum fluorescence intensity (Fmax was less than 10 in three-dimensional fluorescence spectra of excitation wavelength range. When the E167 was added into fresh water based drilling fluid at the dosage of 0.5% (wt/wt, the sticking coefficient reduced rate (ΔKf is 78% and the extreme pressure (E-P friction coefficient reduced rate (Δf is 79%. In the case of 4% brine mud with 0.5% (wt/wt E167 in it, the ΔKf and Δf are 75% and 62%, respectively. After the hot rolling ageing test 180°C × 16 h with the E167 was added into fresh water based drilling fluid at the dosage of 1% (wt/wt, the ΔKf and Δf are greater than 70%, which shows a much better lubrication properties of strong resistance to high temperature. The fresh water based drilling fluid which contains 1% (wt/wt E167 is almost nonfoaming even after hot rolling ageing 120°C × 16 h.

  1. Nitric acid in the stratosphere based on Odin observations from 2001 to 2009 – Part 1: A global climatology

    Directory of Open Access Journals (Sweden)

    J. Urban

    2009-09-01

    Full Text Available The Sub-Millimetre Radiometer (SMR on board the Odin satellite, launched in February 2001, observes thermal emissions of stratospheric nitric acid (HNO3 originating from the Earth limb in a band centred at 544.6 GHz. Height-resolved measurements of the global distribution of nitric acid in the stratosphere were performed approximately on two observation days per week. An HNO3 climatology based on more than 7 years of observations from August 2001 to April 2009 covering the vertical range between typically ~19 and 45 km (~1.5–60 hPa or ~500–1800 K in terms of potential temperature was created. The study highlights the spatial and seasonal variation of nitric acid in the stratosphere, characterised by a pronounced seasonal cycle at middle and high latitudes with maxima during late fall and minima during spring, strong denitrification in the lower stratosphere of the Antarctic polar vortex during winter (the irreversible removal of NOy by the sedimentation of cloud particles containing HNO3, as well as large quantities of HNO3 formed every winter at high-latitudes in the middle and upper stratosphere. A strong inter-annual variability is observed in particular at high latitudes. A comparison with a stratospheric HNO3 climatology, based on over 7 years of UARS/MLS (Upper Atmosphere Research Satellite/Microwave Limb Sounder measurements from the 1990s, shows good consistency and agreement of the main morphological features in the potential temperature range ~465 to ~960 K, if the different characteristics of the data sets such as the better altitude resolution of Odin/SMR as well as the slightly different altitude ranges are considered. Odin/SMR reaches higher up and UARS/MLS lower down in the stratosphere. An overview from 1991 to 2009 of stratospheric nitric acid is provided (with a short gap between 1998 and 2001, if the global measurements of both experiments are taken together.

  2. Reduction of radioactive low-level liquid wastes in a reprocessing plant. Application of electrolysis to nitric acid decomposition -(2)-

    International Nuclear Information System (INIS)

    NOx gas generation by electrolysis of HNO3 has been extensively examined to drastically reduce the quantity of low-level liquid waste from a PUREX reprocessing plant. In this study, benchmark experiments used an electrolysis cell with 700-cm2 electrodes and auxiliary equipment for oxidation and distillation to concentrate a portion of the cathode loop depleted nitric acid, which contained HNO2. The material balance for the NOx-HNO2-HNO3 chemical equilibrium was clarified by the electrolysis. Further, a basic flow diagram was developed for a total system to effectively produce NOx gas. (authors)

  3. Inflence of S and Mn on ICC susceptibility of 02Kh18N13 steel in nitric acid media

    International Nuclear Information System (INIS)

    The paper studies the impact of S and Mn additions on grain boundary stability of annealed and tempered samples of 02Kh18N13 steel in nitric acid media with additions and without ions of hexavalent chromium. A negative impact of the medium and manganese is established for annealed samples which were tempered at 600 deg C for more than 50 h. This effect is presimably related to grain boundary segreagation of sulphur and manganese and accelerating impact of these elements on chromium deplition of the boundaries of sensitized steel grains

  4. Extraction of actinides and fission products by octyl(phenyl)-N,N-diisobutylcarbamoylmethyl-phosphine oxide from nitric acid media.

    Science.gov (United States)

    Mathur, J N; Murali, M S; Natarajan, P R; Badheka, L P; Banerji, A

    1992-05-01

    Extraction of promethium(III), uranium(VI), plutonium(IV), americium(III), zirconium(IV), ruthenium(III), iron(III) and palladium(II) has been carried out with a mixture of octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO) and tributyl phosphate (TBP) in dodecane. The effects of nitric acid, TBP and CMPO concentrations on the extraction of these metal ions have been studied. The nature of the species of the above metal ions extracted into the organic phase has been suggested. PMID:18965406

  5. Precipitation of pertechnetate ion from nitric acid solutions using complexes of copper(II) with heterocyclic N-donor ligands

    International Nuclear Information System (INIS)

    The TcO4- precipitation with organic complexes of Cu(II) from nitric acid solutions was studied. Complex Cu(phen)3(NO3)2 was chosen as the optimal precipitant. The conditions for maximum Tc precipitation of 95 ± 3 % were determined. It was shown the possibility to obtain metal-Tc alloys by thermal treatment of the precipitates. As found, the addition of the fusible metal (Sn) to the sediment was required to receive appropriate matrix. Cu-Tc-Sn matrix was tested for Tc leaching. (author)

  6. Kinetics of mass transfer on a drop bundle in the system uranyl nitrate nitric acid/tributyl phosphate, kerosene

    International Nuclear Information System (INIS)

    The dissertation discusses the kinetics of the coupled exchange of nitric acid and uranyl nitrate between water and tributylphosphate-burdened kerosene. Preliminary to column design, mass exchange measurements were carried out on a monodisperse droplet bundle according to a method not described so far. The concentration range investigated, i.e. 1x10-5 2(NO3)2 -1 kmol/m3, HNO3 = 2,4 kmol/m3, TBP = 30 Vol.% (TBP-Tributylphosphat), meets the technical standards. (orig.)

  7. Reaction of formic and nitric acids with Savannah River Site radioactive HLW sludge in the DWPF pretreatment steps

    International Nuclear Information System (INIS)

    The Defense Waste Processing Facility (DWPF) at the Savannah River Site (SRS) will combine borosilicate frit with highly radioactive waste sludge to produce glass waste forms for disposal. A key step in the DWPF will be acidification of the sludge with formic and nitric acids prior to vitrification. The reducing properties of formic acid will be used to reduce mercury (II) oxide and salts to elemental mercury. The mercury will then be steam-stripped, recovered, and purified. Another benefit of acidifying the sludge will be to reduce its viscosity so that a sludge-frit mixture can be pumped to the melter. The sludge viscosity decreases with pH as various sludge components dissolve with increasing acidity

  8. Study of the properties of dialkyl thiophosphoric acids. Application to the extraction of U, in phosphoric and nitric solutions

    International Nuclear Information System (INIS)

    A study is made of complex formation and liquid-liquid extraction of uranium (VI) by dialkyl-thiophosphoric acids of formula (RO)2POSH and by the synergic mixtures: dialkylthiophosphoric acids-phosphine oxides. The aqueous phases studied consist of concentrated phosphoric acid solutions and nitric acid solutions. Several methods, including distribution coefficient measurements, U.V., visible and infrared absorption spectrophotometries and magnetic resonance, were used to study the extraction mechanisms and the structures of species formed in the organic phase. The influence of different parameters (partition of extraction agent, dimerisation, acid ligand-phosphine oxide association, extraction of inorganic acids...) on the uranium (VI) distribution coefficients enabled the constants of complex formation in the aqueous phase and extraction in the organic phase to be determined. These various properties were compared with those of dialkyl phosphoric and dithiophosphoric acids. The mechanisms established prove that sulfur donors ligands form stable complexes with UO22+ ions although U(VI) is considered as a ''hard class a'' acceptor according to Ahrland's classification

  9. Removal of Pb(II) from water by the activated carbon modified by nitric acid under microwave heating.

    Science.gov (United States)

    Yao, Shuheng; Zhang, Jiajun; Shen, Dekui; Xiao, Rui; Gu, Sai; Zhao, Ming; Liang, Junyu

    2016-02-01

    The rice husk based activated carbon (RH-AC) was treated by nitric acid under microwave heating, in order to improve its capability for the removal of heavy metal ions from water. The optimal conditions for the modification of RH-AC (M-RH-AC) were determined by means of orthogonal array experimental design, giving those as the concentration of nitric acid of 8mol/L, modification time of 15min, modification temperature of 130°C and microwave power of 800W. The characteristics of the M-RH-AC and RH-AC were examined by BET, XRD, Raman spectrum, pH titration, zeta potential, Boehm titration and FTIR analysis. The M-RH-AC has lower pore surface area, smaller crystallite, lower pHIEP and more oxygen-containing functional groups than the RH-AC. Removal capacity of Pb(II) ions by the M-RH-AC and RH-AC from water solution was estimated concerning the influence of contact time, pH value, and initial concentration. The equilibrium time of Pb(II) removal was found to be around 90min after modification process. Two kinetic models are adopted to describe the possible Pb(II) adsorption mechanism, finding that the adsorption rate of Pb(II) ions by the M-RH-AC is larger than that of RH-AC. PMID:26520818

  10. Application of the exergy method to the environmental impact estimation: The nitric acid production as a case study

    International Nuclear Information System (INIS)

    In this work the exergy method is used to compare various methods for removal of NOx from waste (tail) gas released into the atmosphere from nitric acid production plants with respect to their overall environmental impact. Three basic methods for NOx abatement are analysed: selective catalytic reduction (SCR), non-selective catalytic reduction (NSCR) and extended absorption. The positive and negative effects and the net effect from the NOx abatement are calculated. The following exergy-based indicators are used for comparing the energy efficiency and the environmental impact of different treatment processes as a result from pollutants removal: reduction of the exergy of the emissions from the whole process route (ammonia and nitric acid production units); exergy of the additional emissions, arising as a result of the treatment process; total net reduction of the exergy consumption, Cumulative Energy Consumption (CEnC) and Cumulative Exergy Consumption (CExC) of natural resources as a result of the waste flows treatment. -- Highlights: → A thermodynamic study of the effects of three NOx abatement methods. → A comparison of the positive, negative and overall net effects of the three methods. → The best overall results are obtained for the extended absorption method. → The selective catalytic reduction method is estimated as unsatisfactory. → The non-selective catalytic reduction method could benefit from improved catalysts.

  11. Extraction of americium(III) from nitric acid medium by CMPO-TBP extractants in ionic liquid diluent

    International Nuclear Information System (INIS)

    Extraction of americium(III) from nitric acid medium by a solution of tri-n-butylphosphate (TBP) and n-octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO) in room temperature ionic liquid, l-butyl-3-methyl-imidazolium bis(trifluoromethanesulfonyl)imide (bmimNTf2), was studied and the results were compared with that obtained with CMPO-TBP in n-doddecane (n-DD). The distribution ratio of 241Am(III) in TBP-CMPO/bmimNTf2 was measured as a function of various parameters such as concentrations of nitric acid, CMPO, bmimNO3, NaNO3 and TBP and temperature. Remarkably large distribution ratios were observed for the extraction of americium(III) when bmimNTf2 acted as diluent and the extraction was insignificant in the absence of CMPO. The stoichiometry of metal-solvate in organic phase was determined by the slope analysis of extraction data and it indicated the formation of 1:3 (Am: CMPO) complex in organic phase. Viscosity of TBP-CMPO/bmimNTf2 at various temperatures and enthalpy change accompanied by the extraction of americium(III) were determined and reported in this paper. (orig.)

  12. Dialkylmethyl-2-(N,N-diisobutyl)acetamidoammonium iodide as a ruthenium selective ligand from nitric acid medium.

    Science.gov (United States)

    Sharma, Shikha; Ghosh, Sunil K; Sharma, Joti N

    2015-09-15

    A new class of quaternary ammonium iodide based ligands with 2-(N,N-diisobutyl)acetamide as an alkyl appendage have been designed, synthesized and tested for their ability to extract ruthenium selectively from nitric acid medium. The 2-(N,N-diisobutyl)acetamido ammonium iodide with two propyl and a methyl substituents showed best results for the recovery of ruthenium. The optimized concentration of the solvent was found to be 0.2M in 30% isodecyl alcohol/n-dodecane. The stoichiometry of the complex was ascertained by slope analysis method and was found to be 1:1 with respect to ligand L(+)I(-) and Ru(NO)(NO3)3. Ruthenium formed an adduct of structure LRu(NO)(NO3)3 I in the extraction medium. Iodide ion played an important role in the formation of the stable and extractable complex of ruthenium. No extraction was observed when iodide was replaced by nitrate anion in the ligand. The ligand also showed good selectivity for ruthenium in the presence of other metal ions commonly found in nitric acid solutions of nuclear waste. PMID:25863580

  13. Solvent extraction of uranium(VI) and thorium(IV) in nitric acid solution by N,N,N‘,N’—tetrabutyladipicamide

    Institute of Scientific and Technical Information of China (English)

    WangYou-Shao; BaoBo-Rong; 等

    1997-01-01

    N,N,N'N'-tetrabutyladipicamide(TBAA) has been synthesized,and applied to the extraction of U(VI) and Th(IV) from nitric acid solutions in a diluent composed of 0.50 volume fraction 1,2,4-trimethyl benzene (TMA) and 0.50 volume fraction kerosene(OK),The effects of the aueous nitric acid concentration,extractant concentration,slating-out agent (LiNO3) and temperature on extraction ability of TBAA for U(VI) and Th(IV) have been studied.Back Extraction of U(VI) and Th (IV) from organic phases were performed by dilute nitric acid.The compositions of extracted complexes,equilibrium constants and enthalpies of extraction reactions have also been estimated.The IR spectra of extraction of U(VI) and Th(IV) have been studied.

  14. Extraction of uranium(VI) and Thorium(IV) ions from nitric acid solutions by N,N,N',N'-tetrabutyladipicamide

    International Nuclear Information System (INIS)

    A new symmetrical diamide, the straight-chain alkyl substituted neutral tetrabutyladipicamide (TBAA) has been synthesized, characterized and used for the extraction of U(V) and Th(IV) from nitric acid solutions in a diluent composed of 50% 1,2,4-trimethylbenzene (TMB) and 50% kerosene (OK). Extraction distribution coefficients of (U(VI) and Th(IV) as a function of aqueous nitric acid concentration extractant concentration and temperature have been studied. Back-extraction of U(VI) and Th(IV) from organic phases by dilute nitric acid has been undertaken. From the data, the compositions of extracted species, equilibrium constants and enthalpies of extraction reactions have also been calculated. (author). 7 refs., 3 figs., 3 tabs

  15. Tritium distribution ratios between the 30 % tributyl phosphate(TBP)-normal dodecane(nDD) organic phase and uranyl nitrate-nitric acid aqueous phase

    International Nuclear Information System (INIS)

    Tritium distribution ratios between the organic and aqueous phases were measured for the system of 30 % tributyl phosphate(TBP)-normal dodecane(nDD)/uranyl nitrate-nitric acid water. It was confirmed that tritium is extracted by TBP into the organic phase in both chemical forms of tritiated water (HTO) and tritiated nitric acid (TNO3). The value of tritium distribution ratio ranged from 0.002 to 0.005 for the conditions of 0-6 mol/L nitric acid, 0.5-800 mCi/L tritium in aqueous phase, and 0-125 g-U/L uranium in organic phase. Isotopic distribution coefficient of tritium between the organic and aqueous phases was observed to be about 0.95. (author)

  16. 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

    International Nuclear Information System (INIS)

    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

  17. [Effect of tricarboxylic acid cycle intermediates on nitric oxide system during acute hypoxia].

    Science.gov (United States)

    Kurhaliuk, N M

    2002-01-01

    Effects Crebs Cycle of exogenous intermediates sodium succinate (50 mg/kg) and sodium alpha-ketoglutarate (200 mg/kg) on processes of mitochondrial ADP-stimulated respiration (using as substrates of oxidation 0.35 mM succinate, 1 mM alpha-ketoglutarate), production of nitric oxide under NO2-, NO3-, as well as carbamide, putrescyne content and processes of lipid peroxidation in the rats liver under acute hypoxia (7% O2 in N2, 30 min) have been studied. It was shown, that the exogenous sodium alpha-ketoglutarate increases nitric oxide content, aminotransferase activation, inhibition of succinatedehydrogenase simultaneously more than exogenous sodium succinate. It correlates with decreasing of processes lipid peroxidation in liver. PMID:14964867

  18. Estimation of salivary nitric oxide and uric acid levels in oral squamous cell carcinoma and healthy controls

    Directory of Open Access Journals (Sweden)

    Varsha Salian

    2015-01-01

    Full Text Available Background: Oral squamous cell carcinoma (OSCC being the most common head and neck cancer, involves the interplay of several free radicals and antioxidant molecules. The potential role of salivary nitric oxide (NO and uric acid in cancer development needs to be explored as there are a few studies highlighting their association with each other and with oral cancer. Aims: The present study was designed to measure the NO and uric acid levels in the saliva of patients with OSCC as compared with healthy controls and to highlight any possible correlations between them. Materials and Methods: The present study involved 50 subjects, 25 with OSCC (study and 25 healthy individuals (controls. Saliva samples collected from patients were subjected to NO and uric acid analysis by griess method and uricase method, respectively. Statistical Analysis: The results were analyzed using Student′s t-test and Pearson′s Chi-square test. Results: A significant increase in the salivary levels of NO was seen in study subjects as compared to healthy controls. On the contrary, a significant decrease in salivary uric acid level was observed in the study group as compared to healthy controls. In addition, there exists an inverse correlation between NO and uric acid levels in study and control groups. Conclusion: Salivary levels of NO and uric acid may act as key bimolecular markers in the detection of oral cancer, which could be further confirmed by larger sample size and future studies.

  19. New Catalyst for Removal of N2O from Nitric Acid Plant Tail Gases

    OpenAIRE

    Obalová, L.

    2013-01-01

    In the present work, the Co-Mn-Al mixed oxide modified by K was prepared in the pilot plant scale for the first time and tested in real conditions. Result of N2O catalytic decomposition in the pilot plant reactor installed at the bypassed tail gas from the nitric production plant are shown and obtained kinetic datae used for modelling of full scale reactor for N2O emissions abatement.

  20. New Catalyst for Removal of N2O from Nitric Acid Plant Tail Gases

    Czech Academy of Sciences Publication Activity Database

    Obalová, L.; Kovanda, F.; Jirátová, Květa; Šrámek, J.; Karásková, K.; Chromčáková, Ž.; Borovec, K.; Dej, M.

    Praha : Orgit, 2013 - (Kalenda, P.; Lubojacký, J.), s. 319-324 ISBN 978-80-86238-55-5. [International Conference on Chemical Technology (ICCT 2013) /1./. Mkulov (CZ), 08.04.2013-10.04.2013] R&D Projects: GA TA ČR TA01020336 Institutional support: RVO:67985858 Keywords : Co-Mn-Al mixed oxide * nitric production plant * catalyst Subject RIV: CI - Industrial Chemistry, Chemical Engineering

  1. Spectrofluorimetric determination of nitric oxide at trace levels with 5,6-diamino-1,3-naphthalene disulfonic acid.

    Science.gov (United States)

    Zhang, Xian; Wang, Hong; Liang, Shu-Cai; Zhang, Hua-Shan

    2002-03-01

    Based on the selective reaction that 5,6-diamino-1,3-naphthalene disulfonic acid (DANDS) traps nitric oxide (NO) in the presence of dioxygen to yield the highly fluorescent form, 1-[H]-naphthotriazole-6,8-disulfonic acid in moderately alkaline medium, a new spectrofluorimetric method for the determination of NO has been reported. The method offered the advantage of specificity, sensitivity and a simple protocol for the direct detection of NO in aqueous solution. The linear calibration range for NO was 0.04-1.44 mumoll(-1) with a 3sigma detection limit of 0.6 nmoll(-1). The proposed method has been used to monitor the release of NO from S-nitrosocysteine, a NO-releasing agent. PMID:18968522

  2. Extraction of uranium (VI) and plutonium(IV) with some high molecular weight aliphatic monoamides from nitric acid medium

    International Nuclear Information System (INIS)

    The extraction behavior of U(VI) and Pu(IV) with dioctyloctanamide (DOOA), dioctylethylhexanamide (DOEHA) and diisobutylethylhexanamide (DIBEHA) was investigated from nitric acid medium. With DOOA, U(VI) extraction is higher than that for Pu(IV) upto 5M HNO3 and the trend is reversed at higher acid concentrations. Extraction yield of U(VI) is higher than that for Pu(IV) in the case of DOEHA and DIBEHA. DIBEHA extraction of Pu(IV) is found to be very small. The lower value of the distribution ratio for Pu(IV) with branched amides was attributed to steric reasons. The possibility of using these amides for separation of U(VI) and Pu(IV) without valency adjustment was explored. Both U(VI) and Pu(IV) are extracted as their disolvates by DOOA and DOEHA. (author) 12 refs.; 5 figs.; 2 tabs

  3. A high linoleic acid diet increases oxidative stress in vivo and affects nitric oxide metabolism in humans.

    Science.gov (United States)

    Turpeinen, A M; Basu, S; Mutanen, M

    1998-09-01

    Evidence from in vitro studies shows that increased intake of polyunsaturated fatty acids leads to increased oxidative stress, which may be associated with endothelial damage. We measured the urinary levels of 8-iso-PGF2alpha and nitric oxide metabolites as well as plasma sICAM-1 levels from healthy subjects after strictly controlled diets rich in either linoleic acid (LA, C18:2 n-6) or oleic acid (OA, C18:1 n-9). Thirty-eight volunteers (20 women and 18 men, mean age 27 years) consumed a baseline diet rich in saturated fatty acids (SFA) for 4 weeks and were then switched to either a high LA diet (11.5 en%) or a high OA diet (18.0 en%) also for 4 weeks. During the LA and OA diets, nearly all food was provided for the whole day. A control group of 13 subjects consumed their habitual diet throughout the study. Urinary excretion of 8-iso-PGF2alpha was significantly increased after the LA diet (170 vs 241 ng/mmol creatinine, P=0.04), whereas the urinary concentration of nitric oxide metabolites decreased (4.2 vs 2.6 mg/mmol creatinine, P=0.03). No significant changes were seen in the OA group. Significant differences between the LA and control group were found for both 8-oxo-PGF2alpha (P=0.03) and NO (P=0.02), whereas the OA and LA groups did not differ with respect to any parameter. Also plasma sICAM-1 remained unchanged in both groups throughout the study. In conclusion, the high-LA diet increased oxidative stress and affected endothelial function in a way which may in the long-term predispose to endothelial dysfunction. PMID:9844997

  4. Distribution of Components in Ion Exchange Materials Taken from the K East Basin and Leaching of Ion Exchange Materials by Nitric/Hydrofluoric Acid and Nitric/Oxalic Acid

    International Nuclear Information System (INIS)

    Laboratory tests were performed to examine the efficacy of mixed nitric/hydrofluoric acid followed by mixed nitric/oxalic acid leach treatments to decontaminate ion exchange materials that have been found in a number of samples retrieved from K East (KE)Basin sludge. The ion exchange materials contain organic ion exchange resins and zeolite inorganic ion exchange material. Based on process records, the ion exchange resins found in the K Basins is a mixed-bed, strong acid/strong base material marketed as Purolite NRW-037. The zeolite material is Zeolon-900, a granular material composed of the mineral mordenite. Radionuclides sorbed or associated with the ion exchange material can restrict its disposal to the Environmental Restoration Disposal Facility (ERDF). The need for testing to support development of a treatment process for K Basin sludge has been described in Section 4.2 of ''Testing Strategy to Support the Development of K Basins Sludge Treatment Process'' (Flament 1998). Elutriation and washing steps are designed to remove the organic resins from the K Basin sludge. To help understand the effects of the anticipated separation steps, tests were performed with well-rinsed ion exchange (IX) material from KE Basin floor sludge (sample H-08 BEAD G) and with well-rinsed IX having small quantities of added KE canister composite sludge (sample KECOMP). Tests also were performed to determine the relative quantities of organic and inorganic IX materials present in the H-08 K Basin sludge material. Based on chemical analyses of the separated fractions, the rinsed and dry IX material H-08 BEAD G was found to contain 36 weight percent inorganic material (primarily zeolite). The as-received (unrinsed) and dried H-08 material was estimated to contain 45 weight percent inorganic material

  5. Separating cesium 137 from liquid radioactive wastes by using inorganic exchangers using static and dynamic procedures at various concentration of nitric acid and sodium nitrate

    International Nuclear Information System (INIS)

    Cesium 137 was separated from liquid wastes by ion exchange using ammonium molybdenum phosphate, potassium hexa cyano cobalt ferrate, zirconium hydro phosphate and antimony penta oxy hydrate ion exchangers. The investigation was done by static and dynamic procedures. In static procedure required time for reaching the system to equilibrium or ion exchange completion, the measurement of each exchanger, the effect of nitric acid and concentration of sodium nitrate on the capacity of ion exchangers was investigated. Also in dynamic procedure nitric acid and sodium nitrate concentration ratio on the power of and thereof the capacity of each ion exchanger was determined

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-08-28

    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.

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2012-05-07

    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.

  8. Fatty acid-binding protein 4 impairs the insulin-dependent nitric oxide pathway in vascular endothelial cells

    Directory of Open Access Journals (Sweden)

    Aragonès Gemma

    2012-06-01

    Full Text Available Abstract Background Recent studies have shown that fatty acid-binding protein 4 (FABP4 plasma levels are associated with impaired endothelial function in type 2 diabetes (T2D. In this work, we analysed the effect of FABP4 on the insulin-mediated nitric oxide (NO production by endothelial cells in vitro. Methods In human umbilical vascular endothelial cells (HUVECs, we measured the effects of FABP4 on the insulin-mediated endothelial nitric oxide synthase (eNOS expression and activation and on NO production. We also explored the impact of exogenous FABP4 on the insulin-signalling pathway (insulin receptor substrate 1 (IRS1 and Akt. Results We found that eNOS expression and activation and NO production are significantly inhibited by exogenous FABP4 in HUVECs. FABP4 induced an alteration of the insulin-mediated eNOS pathway by inhibiting IRS1 and Akt activation. These results suggest that FABP4 induces endothelial dysfunction by inhibiting the activation of the insulin-signalling pathway resulting in decreased eNOS activation and NO production. Conclusion These findings provide a mechanistic linkage between FABP4 and impaired endothelial function in diabetes, which leads to an increased cardiovascular risk.

  9. The Meteorology and Chemistry of High Nitric-Acid Episodes at the South Pole

    Science.gov (United States)

    Neff, William; Davis, Douglas

    2016-04-01

    Between 1998 and 2007, a series of field experiments carried out at the South Pole and with aircraft over a wider area revealed a very chemically active boundary layer overlying the east Antarctic ice sheet during the Austral summer. An early discovery was unexpectedly high concentrations of nitric acid (NO) at the South Pole. These were argued to be a result of the UV pholoysis of reactive nitrogen in surface and/or near-surface snow followed by subsequent confinement and non-linear HOx/NOx chemistry within a thin stable atmospheric boundary layer. The concentrations of NO also demonstrated daily, intraseasonal, as well as interannual variability as seen in the four field programs. This paper seeks to elucidate the interplay of large-to-small scale meteorology and chemistry at the South Pole that leads to highly variable NO concentrations and to examine boundary layer depth effects on NO in years when no direct measurements were available, in particular during the latest field program in 2006-2007. The importance of the South Pole is that it, unlike other high-latitude sites, has no diurnal cycle to disturb the evolution of the mostly stable boundary layer and its physics and chemistry. In the spring, as the solar elevation angle increases, nitrate photolysis rates increase. At the same time, the stratospheric vortex warms and with its breakup, the total column ozone increases leading to decreased photolysis rates. In addition, following the formation of the thermal tropopause in early spring, the tropospheric circulation over Antarctica changes dramatically, affecting the transport and dominant source regions for warm air and clouds arriving at the South Pole. The timing of the final warming ranged from early-November to mid-December for the four field experiment years. During the 30 days prior to the final increase in column ozone, as the thermal tropopause forms (~100 hPa), the winds at 300 hPa become bimodal, either along the eastern side of the Weddell Sea

  10. Microwave-assisted digestion using nitric acid for heavy metals and sulfated ash testing in active pharmaceutical ingredients.

    Science.gov (United States)

    Pluhácek, T; Hanzal, J; Hendrych, J; Milde, D

    2016-04-01

    The monitoring of inorganic impurities in active pharmaceutical ingredients plays a crucial role in the quality control of the pharmaceutical production. The heavy metals and residue on ignition/sulfated ash methods employing microwave-assisted digestion with concentrated nitric acid have been demonstrated as alternatives to inappropriate compendial methods recommended in United States Pharmacopoeia (USP) and European Pharmacopoeia (Ph. Eur.). The recoveries using the heavy metals method ranged between 89% and 122% for nearly all USP and Ph. Eur. restricted elements as well as the recoveries of sodium sulfate spikes were around 100% in all tested matrices. The proposed microwave-assisted digestion method allowed simultaneous decomposition of 15 different active pharmaceutical ingredients with sample weigh up to 1 g. The heavy metals and sulfated ash procedures were successfully applied to the determination of heavy metals and residue on ignition/sulfated ash content in mycophenolate mofetil, nicergoline and silymarin. PMID:27209695

  11. Microstructure and Corrosion Behavior of Hf-40 Wt Pct Ti Alloy in Nitric Acid Medium for Reprocessing Applications

    Science.gov (United States)

    Jayaraj, J.; Ravi, K. R.; Mallika, C.; Kamachi Mudali, U.

    2016-09-01

    The Hf-40 wt pct Ti (Hf-Ti) alloy was developed for neutron poison application in the spent nuclear fuel reprocessing plant. The furnace-cooled Hf-Ti sample exhibited the microstructure comprising equiaxed-α, lamellar-α, and feathery-α. The water-quenched Hf-Ti sample confirmed the presence of lath and internally twinned martensite. In comparison to the furnace-cooled sample, low corrosion current density and passivation current density values obtained for the water-quenched Hf-Ti in 6 M HNO3 at 298 K (25 °C) indicated better passivation ability. The martensitic structure exhibited high hardness (660 HV) and negligible corrosion rate in 6 M nitric acid at 298 K (25 °C). X-ray photoelectron spectroscopic (XPS) analysis confirmed that passivation behavior of this alloy was due to the protective passive film composed of TiO2 and HfO2.

  12. Hydrofluoric-nitric-sulphuric-acid surface treatment of tungsten for carbon fibre-reinforced composite hybrids in space applications

    Science.gov (United States)

    Kanerva, M.; Johansson, L.-S.; Campbell, J. M.; Revitzer, H.; Sarlin, E.; Brander, T.; Saarela, O.

    2015-02-01

    Hybrid material systems, such as combinations of tungsten foils and carbon fibre-reinforced plastic (CFRP), are replacing metal alloy concepts in spacecraft enclosures. However, a good adhesion between the tungsten oxide scale and the epoxy resin used is required. Here, the effects of a hydrofluoric-nitric-sulphuric-acid (HFNS) treatment on tungsten oxides and subsequent adhesion to CFRP are analysed using atomic force microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and fracture testing. The work shows that HFNS treatment results in decreased oxygen content, over 50% thinner tungsten trioxide (WO3) layer and increased nano-roughness on thin tungsten foils. Fracture testing established a 39% increase in the average critical strain for tungsten-CFRP specimens after HFNS treatment was carried out on tungsten. The effect of the oxide scale modification regarding the critical strain energy release rate was ΔGc≈ 8.4 J/m2.

  13. Separation of rare earths in nitric acid medium by a novel silica-based pyridinium anion exchange resin

    International Nuclear Information System (INIS)

    To separate rare earths in nitric acid medium by anion exchange process, a novel silica-based macro-reticular anion exchange resin (SiPyR-N4) with pyridinium as functional group has been synthesized. It was found that the SiPyR-N4 resin exhibits a quite strong adsorption for some rare earths especially the light rare earth elements such as La, Ce, Pr, Nd and Pm whose distribution coefficients onto SiPyR-N4 reach 10-25 dm3/kg-resin, which are much higher than the reported values for these elements with conventional anion exchange resins. The results from the column experiments show that the rare earths can be separated into the three groups: light, moderate and heavy rare earths and, a perfect separation between La-Pr group and Sm-Gd group can be achieved

  14. Soft cutting of single-wall carbon nanotubes by low temperature ultrasonication in a mixture of sulfuric and nitric acids

    International Nuclear Information System (INIS)

    To decrease single-wall carbon nanotube (SWCNT) lengths to a value of 100–200 nm, aggressive cutting methods, accompanied by a high loss of starting material, are frequently used. We propose a cutting approach based on low temperature intensive ultrasonication in a mixture of sulfuric and nitric acids. The method is nondestructive with a yield close to 100%. It was applied to cut nanotubes produced in three different ways: gas-phase catalysis, chemical vapor deposition, and electric-arc-discharge methods. Raman and Fourier transform infrared spectroscopy were used to demonstrate that the cut carbon nanotubes have a low extent of sidewall degradation and their electronic properties are close to those of the untreated tubes. It was proposed to use the spectral position of the far-infrared absorption peak as a simple criterion for the estimation of SWCNT length distribution in the samples. (paper)

  15. Synergistic extraction of U(VI) and Th(IV) from nitric acid with HBMPPT and PSO in toluene

    International Nuclear Information System (INIS)

    The synergistic extraction of U(VI) and Th(IV) from nitric acid solution by HBMPPT (4-benzoyl-2, 4-dihydro-5-methyl-2-phenyl-3H-pyrazol-3-thione) and PSO (Petroleum Sulfoxide) in toluene is studied. The extraction ability of HBMPPT is not as high as that of its parent (HBMPP), but the addition of a little amount of PSO significantly improved the extraction ability to U(VI), while the ability to extract Th(IV) is slightly increased. The synergistically extracted complexes may be presented as UO2(BMPPT)2·PSO for U(VI), and Th (NO3)2(BMPPT)2·PSO for Th(IV), respectively. The separation coefficient is about 1000 under certain condition when HBMPPT-PSO is used to separate U(VI) and Th(IV)

  16. Influence of external magnetic field on the etching of a steel ball in an aqueous solution of nitric acid

    International Nuclear Information System (INIS)

    The effect of change of shape of a steel ball was revealed as a result of its etching in an aqueous solution of nitric acid under influence of an external magnetic field. The elongation of a ferromagnetic ball was observed along the direction of an external magnetic field while etching took place uniformly in all the directions without magnetic field application. The steel ball etching in a magnetic field is characterized by formation of three cylindrically symmetric regions with different etching rates and surface structures, divided from each other by clear borders (namely, the pole, equator and transition regions are formed). The non-monotone dependences of etching rate, surface structure of a sample and sample shape after etching on an external magnetic field are observed.

  17. Microstructure and Corrosion Behavior of Hf-40 Wt Pct Ti Alloy in Nitric Acid Medium for Reprocessing Applications

    Science.gov (United States)

    Jayaraj, J.; Ravi, K. R.; Mallika, C.; Kamachi Mudali, U.

    2016-06-01

    The Hf-40 wt pct Ti (Hf-Ti) alloy was developed for neutron poison application in the spent nuclear fuel reprocessing plant. The furnace-cooled Hf-Ti sample exhibited the microstructure comprising equiaxed-α, lamellar-α, and feathery-α. The water-quenched Hf-Ti sample confirmed the presence of lath and internally twinned martensite. In comparison to the furnace-cooled sample, low corrosion current density and passivation current density values obtained for the water-quenched Hf-Ti in 6 M HNO3 at 298 K (25 °C) indicated better passivation ability. The martensitic structure exhibited high hardness (660 HV) and negligible corrosion rate in 6 M nitric acid at 298 K (25 °C). X-ray photoelectron spectroscopic (XPS) analysis confirmed that passivation behavior of this alloy was due to the protective passive film composed of TiO2 and HfO2.

  18. First Analysis of the ν_5 Band of DNO_3 (deuterated Nitric Acid) in the 11 μm Region

    Science.gov (United States)

    Koubek, J.; Perrin, A.; Beckers, H.; Willner, H.

    2009-06-01

    The infrared spectrum of DNO_3 (deuterated nitric acid) was recorded at high resolution (0.0018 cm ^{-1}) in the 800 -1400 cm ^{-1} region on the Bruker IFR 120 HR Fourier transform spectrometer of Wuppertal. The analysis of the ν_5 A-type band of DNO_3 centered at 887.656 cm ^{-1} was performed taking use of the ground state parameters achieved by Drouin et al. This band is perturbed by several resonances. [1] Drouin, Miller, Fry, Petkie, Helminger, Medvedev, J. Mol. Spectrosc. 236 (2006) 29-34 [2] Acknowledgment: The work was supported through the Ministry of Education, Youth and Sports of the Czech Republic (research program LC06071) and scholarship of the French government (Bourse du Gouvernement Francais - Bourse de Doctorat en co-tutelle).

  19. Violent explosion after inadvertent mixing of nitric acid and isopropanol – Review 15 years later finds basic accident data corrupted, no evidence of broad learning

    DEFF Research Database (Denmark)

    Hedlund, Frank Huess; Folmer Nielsen, Merete; Hagen Mikkelsen, Sonja;

    2014-01-01

    to produce isopropyl nitrate (nitric acid 1-methylethyl ester, CAS 1712-64-7), a rocket propellant. It is argued that the accident has broad learning potential because of the widespread usage of the two chemicals across industries, the innocent nature of the human error and the severity of the...

  20. TBP 20% - diluent/HNO3/H2O liquid-liquid extraction system: equilibrium normalization data of nitric acid, ruthenium and zirconium

    International Nuclear Information System (INIS)

    The extraction behaviour of nitric acid, nitrosyl-ruthenium nitrate and zirconium hydroxide nitrate in the system tri-n-butyl phosphate (TBP) 20% - diluent was studied. The main purpose was to obtain enough data to elaborate process flowsheets for the treatment of irradiated uranium fuels. During the runs, the equilibrium diagrams of nitric acid, ruthenium and zirconium were settled. From the achieved data, the influence of nitric acid, ruthenium, zirconium and nitrate ions concentration in the aqueous phase was checked. Furthermore, the density and the surface tension of the aqueous and organic phases were determined, gathering the interfacial tension after the contact between the phases. A comparison among the obtained equilibrium data and the existing one from literature allowed the elaboration of mathematical models to express the distribution behaviour of nitric acid, ruthenium and zirconium as a function of nitrate ions concentration in the aqueous phase. The reduction of TBP concentration from 30% v/v (normally used) to 20% v/v, has shown no influence in the extraction behaviour of the elements. A decreasing in the distribution values was observed and that means an important factor during the decontamination of uranium from its contaminants, ruthenium and zirconium. (Author)

  1. Study of the occurrence of synergic effect in the extraction of uranium from nitric and sulphuric acid solutions by mixtures of tri-N-butyl phosphate and di - (2 - ethylhexyl) phosphoric acid

    International Nuclear Information System (INIS)

    The study of synergic effect arising when uranium(VI) is extracted from nitric and sulphuric acid solutions by a mixture of tri-n-butyl phosphate (TBP) and di-(2-ethylhexyl) phosphoric acid (HDEHP) is presented. (A.R.H.)

  2. Solvent extraction of nitric acid, uranium (VI) and thorium (IV) by N, N, N', N'-tetrahexylsuccinylamide

    International Nuclear Information System (INIS)

    A new kind of diamide N,N,N',N'-tetrahexylsuccinylamide (THSA) was synthesized, characterized and used for the extraction of HNO3, U(VI) and Th(IV) in a diluent composed of 0.5 volume fraction 1,2,4-trimethyl benzene (TMB) and 0.5 volume fraction kerosene (OK). Extraction distribution coefficients of U(VI) and Th(IV) as functions of aqueous nitric acid concentration, extractant concentration, temperature and salting-out agent (LiNO3) have been studied, and it is found that THSA as an extractant is superior to TBP for extraction of U(VI) and Th(IV). Back extraction was also studied. At low acidity, the main adduct of THSA and HNO3 is HNO3·THSA. THSA·(HNO3)2 and THSA·(HNO3)3 are also found at high acidity. The compositions of extracted species, apparent equilibrium constants and enthalpies of extraction reactions have also been calculated

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

    International Nuclear Information System (INIS)

    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)

  4. EVALUATION OF ANTIPEROXIDATIVE POTENTIAL OF ASCORBIC ACID ON BUSULFAN-INDUCED LIPID PEROXIDATION USING 4-HYDROXY-2-NONENAL AND NITRIC OXIDE AS MODEL MARKERS

    OpenAIRE

    Supratim Ray

    2012-01-01

    The study was designed with an aim to evaluate the antiperoxidative potential of ascorbic acid on busulfan-induced lipid peroxidation. The study was performed in vitro using goat liver as lipid source. This evaluation was done by measuring the 4-hydroxy-2-nonenal (4-HNE) and nitric oxide (NO) content of liver tissue homogenates as markers of lipid peroxidation. The study reveals the lipid peroxidation induction capacity of busulfan and the antiperoxidative potential of ascorbic acid on busulf...

  5. Phosphorylation of N-methyl-D-aspartic acid receptor-associated neuronal nitric oxide synthase depends on estrogens and modulates hypothalamic nitric oxide production during the ovarian cycle.

    OpenAIRE

    Parkash, Jyoti; d'Anglemont de Tassigny, Xavier; Bellefontaine, Nicole; Campagne, Celine; Mazure, Danièle; Buée-Scherrer, Valérie; Prevot, Vincent

    2010-01-01

    Within the preoptic region, nitric oxide (NO) production varies during the ovarian cycle and has the ability to impact hypothalamic reproductive function. One mechanism for the regulation of NO release mediated by estrogens during the estrous cycle includes physical association of the calcium-activated neuronal NO synthase (nNOS) enzyme with the glutamate N-methyl-d-aspartate (NMDA) receptor channels via the postsynaptic density 95 scaffolding protein. Here we demonstrate that endogenous vari...

  6. Nitric Oxide Mediates 5-Aminolevulinic Acid-Induced Antioxidant Defense in Leaves of Elymus nutans Griseb. Exposed to Chilling Stress.

    Directory of Open Access Journals (Sweden)

    Juanjuan Fu

    Full Text Available Nitric oxide (NO and 5-aminolevulinic acid (ALA are both extremely important signalling molecules employed by plants to control many aspects of physiology. In the present study, the role of NO in ALA-induced antioxidant defense in leaves of two sources of Elymus nutans Griseb. (Damxung, DX and Zhengdao, ZD was investigated. Chilling stress enhanced electrolyte leakage, accumulation of malondialdehyde (MDA, hydrogen peroxide (H2O2 and superoxide radical in two E. nutans, which were substantially alleviated by exogenous ALA and NO application. Pretreatment with NO scavenger PTIO or NOS inhibitor L-NNA alone and in combination with ALA induced enhancements in electrolyte leakage and the accumulation of MDA, H2O2 and superoxide radical in leaves of DX and ZD exposed to chilling stress, indicating that the inhibition of NO biosynthesis reduced the chilling resistance of E. nutans and the ALA-enhanced chilling resistance. Further analyses showed that ALA and NO enhanced antioxidant defense and activated plasma membrane (PM H+-ATPase and decreased the accumulation of ROS induced by chilling stress. A pronounced increase in nitric oxide synthase (NOS activity and NO release by exogenous ALA treatment was found in chilling-resistant DX plants exposed to chilling stress, while only a little increase was observed in chilling-sensitive ZD. Furthermore, inhibition of NO accumulation by PTIO or L-NNA blocked the protective effect of exogenous ALA, while both exogenous NO treatment and inhibition of endogenous NO accumulation did not induce ALA production. These results suggested that NO might be a downstream signal mediating ALA-induced chilling resistance in E. nutans.

  7. Cross-talk between calcium-calmodulin and nitric oxide in abscisic acid signaling in leaves of maize plants

    Institute of Scientific and Technical Information of China (English)

    Jianrong Sang; Aying Zhang; Fan Lin; Mingpu Tan; Mingyi Jiang

    2008-01-01

    Using pharmacological and biochemical approaches,the signaling pathways between hydrogen peroxide (H2O2),calcium (Ca2+)-calmodulin (CAM),and nitric oxide (NO) in abscisic acid (ABA)-induced antioxidant defense were investigated in leaves of maize (Zea mays L.) plants.Treatments with ABA,H2O2,and CaCI2 induced increases in the generation of NO in maize mesophyll cells and the activity of nitric oxide synthase (NOS) in the cytosolic and microsomal fractions of maize leaves.However,such increases were blocked by the pretreatments with Ca2+ inhibitors and CaM antagonists.Meanwhile,pretreatments with two NOS inhibitors also suppressed the Ca2+-induced increase in the production of NO.On the other hand,treatments with ABA and the NO donor sodium nitroprusside (SNP) also led to increases in the concentration of cytosolic Ca2+ in protoplasts of mesophyll cells and in the expression of calmodulin 1 (CaMI) gene and the contents of CaM in leaves of maize plants,and the increases induced by ABA were reduced by the pretreatments with a NO scavenger and a NOS inhibitor.Moreover,SNP-induced increases in the expression of the antioxidant genes superoxide dismutase 4 (SOD4),cytosolic ascorbate peroxidase (cAPX),and glutathione reductase 1 (GRI) and the activities of the chloroplastic and cytosolic antioxidant enzymes were arrested by the pretreatments with Ca2+ inhibitors and CaM antagonists.Our results suggest that Ca2+-CaM functions both upstream and downstream of NO production,which is mainly from NOS,in ABA- and H2O2-induced antioxidant defense in leaves of maize plants.

  8. Production of 15N-enriched nitric acid (H15NO3

    Directory of Open Access Journals (Sweden)

    C. R. Sant Ana Filho

    2008-12-01

    Full Text Available Techniques that employ 15N have proved to be an important tool in many areas of the agronomic and biomedical sciences. Nevertheless, their use is limited by methodological difficulties and by the price of compounds in the international market. Nitric compounds (15NO3- have attracted the interest of researchers. However, these compounds are not currently produced in Brazil. Thus, in the present work H15NO3 was obtained from the oxidation of anhydrous 15NH3. The method we used differs from the industrial process in that the absorption tower is replaced with a polytetrafluoroethylene-lined, stainless-steel hydration reactor. The process output was evaluated based on the following parameters: reaction temperature; ratio of reagents; pressure and flow of 15NH3(g through the catalyst (Pt/Rh. The results showed that, at the best conditions (500 ºC; 50 % excess O2; 0.4 MPa; and 3.39 g.min-1 of 15NH3, a conversion percentage (N-15NH3 to N-15NO3- of 62.2 %, an overall nitrogen balance (N-15NH3 + N-15NO3- of 86.8 %, and purity higher than 99 % could be obtained.

  9. Macro level extraction of U(VI) and Pu(IV) by tri-iso-amyl phosphate and tri-n-butyl phosphate from nitric acid media

    International Nuclear Information System (INIS)

    Batch extraction of Pu(IV) by 1.1 M Tri-iso-amyl phosphate (TiAP) in n-dodecane (DD) from plutonium nitrate solutions in nitric acid media has been investigated as a function of metal loading and equilibrium aqueous phase acidity at 303 K under high solvent loading conditions. Co-extraction behavior of U(VI) and Pu(IV) with 1.1 M solutions of trialkyl phosphates (TBP and TiAP) in n-DD from nitric acid media has also been compared by carrying out the extraction from a U-Pu feed solution (21% Pu to mimic PFBR MOX fuel composition) at 303 K. (author)

  10. Oxytocin induces penile erection when injected into the ventral subiculum: role of nitric oxide and glutamic acid.

    Science.gov (United States)

    Melis, Maria Rosaria; Succu, Salvatora; Cocco, Cristina; Caboni, Emanuela; Sanna, Fabrizio; Boi, Antonio; Ferri, Gian Luca; Argiolas, Antonio

    2010-06-01

    Oxytocin (100 ng) induces penile erection when injected unilaterally into the ventral subiculum of the hippocampus of male rats. The pro-erectile effect started mostly 30 min after treatment and occurred 15 min after an increase in both nitric oxide (NO) production, measured by the concentration of NO(2)(-) and NO(3)(-), the main metabolites of newly formed NO, and extra-cellular glutamic acid concentration in the dialysate obtained from the ventral subiculum by intracerebral microdialysis. These responses were abolished by d(CH(2))(5)Tyr(Me)(2)-Orn(8)-vasotocin (2 microg), an oxytocin receptor antagonist, S-methyl-L-thiocitrulline (SMTC), a selective inhibitor of neuronal NO-synthase (25 microg), and haemoglobin, a NO scavenger (25 microg), given into the ventral subiculum before oxytocin. Unlike d(CH(2))(5)Tyr(Me)(2)-Orn(8)-vasotocin, SMTC and haemoglobin, (+)MK-801 (5 microg), a noncompetitive antagonist of NMDA receptors abolished oxytocin-induced penile erection, but reduced only partially the increase in NO production and extra-cellular glutamic acid. As NMDA (0.25-1 microg) injected into the ventral subiculum induces penile erection episodes, which also occurred with an increase of NO production and extra-cellular glutamic acid, and NMDA responses were abolished by (+)MK-801 (5 microg), but not by SMTC (25 microg) or haemoglobin (25 microg), injected into the ventral subiculum, these results show that oxytocin injected into the ventral subiculum increases NO production by activating its own receptors. NO in turn increases glutamic acid neurotransmission, leading to penile erection, possibly through neural (glutamatergic) efferent projections from the ventral subiculum to extra-hippocampal brain areas (e.g., prefrontal cortex) modulating the activity of mesolimbic dopaminergic neurons. PMID:20156463

  11. The influence of oxidation with nitric acid on the preparation and properties of active carbon enriched in nitrogen

    Science.gov (United States)

    Pietrzak, Robert; Nowicki, Piotr; Wachowska, Helena

    2009-01-01

    The effect of oxidation by 20% nitric acid on the properties and performance of active carbons enriched with nitrogen by means of the reaction with urea in the presence of air has been studied. The study has been made on demineralised orthocoking coal and the carbonisates obtained from it at 600 or 700 °C, subjected to the processes of nitrogenation, oxidation and activation with KOH in different sequences. The amount of nitrogen introduced into the carbon with the aid of urea has been found to depend on the stage at which the process of nitrogenation was performed. The process of oxidation of the demineralised coal and the active carbon obtained from the former has been found to favour nitrogen introduction into the carbon structure. In the process of nitrogenation of the carbonisates the amount of nitrogen introduced has inversely depended on the temperature of carbonisation. The modifications of the processes permitted obtaining materials of different textural parameters, different acid-base character of the surface and different iodine sorption capacity.

  12. The influence of oxidation with nitric acid on the preparation and properties of active carbon enriched in nitrogen

    International Nuclear Information System (INIS)

    The effect of oxidation by 20% nitric acid on the properties and performance of active carbons enriched with nitrogen by means of the reaction with urea in the presence of air has been studied. The study has been made on demineralised orthocoking coal and the carbonisates obtained from it at 600 or 700 deg. C, subjected to the processes of nitrogenation, oxidation and activation with KOH in different sequences. The amount of nitrogen introduced into the carbon with the aid of urea has been found to depend on the stage at which the process of nitrogenation was performed. The process of oxidation of the demineralised coal and the active carbon obtained from the former has been found to favour nitrogen introduction into the carbon structure. In the process of nitrogenation of the carbonisates the amount of nitrogen introduced has inversely depended on the temperature of carbonisation. The modifications of the processes permitted obtaining materials of different textural parameters, different acid-base character of the surface and different iodine sorption capacity.

  13. N,N,N',N'-tetrahexylsuccinylamide as a new extractant for the extraction of nitric acid, uranium(VI) and thorium(IV) ions

    International Nuclear Information System (INIS)

    N,N,N',N'-tetrahexylsuccinylamide (THSA) was used for the extraction of U(VI) and Th(IV) ions from nitric acid media into n-dodecane. Extraction distribution ratios of U(VI) and Th(IV) as a function of nitric acid concentration, extractant concentration and temperature have been studied. It was found that THSA as a new extractant is superior in some aspects to TBP for extraction of U(VI) and Th(IV). The extraction of nitric acid was also investigated. At low acidity, the main adduct of THSA and HNO3 is THSA x HNO3. THSA x (HNO3)2 and THSA x (HNO3)3 also formed at high acidity. The composition of the species, equilibrium constants and enthalpies of the extraction reactions have also been calculated. The suggested formation of the 1:2:1 ratio of uranyl(IV) ion and the 1:4:2 ratio of thorium(IV) ion, nitrate ion and THSA as the extracted species was further confirmed by the IR spectra of U(VI) and Th(IV) extracts. (author)

  14. Determination of Uranyl Nitrate and Nitric Acid Based on Density and Conductivity Measurements

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    <正>Measurement of the uranium and acidity plays an important role in process control of spent fuel reprocessing. The main chemical compositions including a mount of U solution in spent fuel reprocessing

  15. Development of a Technology for Treating Wastewater Contaminated with Nitric Acid

    Directory of Open Access Journals (Sweden)

    Liz Mabel Ríos Hidalgo

    2013-01-01

    Full Text Available The production process of nitroaromatic hazardous compounds, with the generation of acidic wastewater, represents a significant danger for the health and safety of the workers and the environment. The present study is focused on the development of an efficient installation to treat acidic wastewater resulting from the synthesis process of nitroaromatic compound, considering workers safety and environmental criteria. In this research, a detailed study of the different alternatives that can be used for effective and safe treatment of acidic wastewater was performed. The analysis of several technological schemes for the acidic wastewaters neutralization and the selection of the most feasible alternative from a technical-economic point of view were carried out. The simulation and mathematical modeling developed in this research represent a significant advance in the knowledge of this process for working in a much more secure form. The technological scheme of the process was defined, and the design of the main and auxiliary equipment as well as the piping system was carried out using different computational programs. Finally, this paper proposes a technological design for the treatment of acidic wastewater generated by the production process of nitroaromatic compound, which represents the basic criteria for the further design, construction, and equipment installation of the plant.

  16. Selective removal of Ag+ ions from nitric acid medium by alginate microcapsules, Lewatite TP 214 chelating resin, and 200 CT strongly acidic ion exchanger

    International Nuclear Information System (INIS)

    Alginate microcapsules containing bis (2, 4, 4-trimethylpenthyl) monothiophosphinic acid (Cyanex 302) were prepared for the selective removal of Ag+ ions from the reprocessing effluents of FBR-MOX fuel. The Ag+ ions are added for the adjustment of oxidation state of Plutonium. We compared uptake properties of aforementioned microcapsules with those of 200 CT a strongly acidic resin, and Lewatite TP 214, a very selective chelating resin for the Ag+ ions. Most of the uptake properties of the microcapsules were amid the 200 CT and Lewatite, and rather similar to the later. The order of uptake kinetic and breakthrough capacity were the same as: 200 CT > Microcapsules > Lewatite; and for selectivity: Lewatite > Microcapsules > 200 CT. However, high selectivity of Lewatite is rather disadvantageous because it makes the elution operation complicated. Advantages of microcapsules include simple preparation procedure, relatively high selectivity and ease of elution even with 3M nitric acid. However, their total capacity is low. For enhancing the total capacity only increasing the active component is not enough since it deteriorates the kinetics, and the new preparation techniques are necessary which are under study. (author)

  17. Interactions of Gas-Phase Nitric/Nitrous Acids and Primary Organic Aerosol in the Atmosphere of Houston, TX

    Science.gov (United States)

    Ziemba, L. D.; Griffin, R. J.; Dibb, J. E.; Anderson, C. H.; Whitlow, S. I.; Lefer, B. L.; Flynn, J.; Rappenglück, B.

    2007-12-01

    Concentrations of aerosol and gas-phase pollutants were measured on the roof of an 18-story building during the Texas Air Quality Study II Radical and Aerosol Measurement Project (TRAMP) from August 15 through September 28, 2006. Aerosol measurements included size-resolved, non-refractory mass concentrations of ammonium, nitrate, sulfate, chloride, and organic aerosol in submicron particles using an Aerodyne quadrupole aerosol mass spectrometer (Q-AMS). Particulate water-soluble organic carbon (PWSOC) was quantified using a mist chamber/total organic carbon analysis system. Concentration data for gas-phase pollutants included those for nitric acid (HNO3), nitrous acid (HONO), and hydrochloric acid (HCl) collected using a mist chamber/ion chromatographic technique, oxides of nitrogen (NOx) collected using a chemiluminescent method, and carbon monoxide (CO) collected using an infrared gas correlation wheel instrument. Coincident increases in nitrate and organic aerosol mass concentrations were observed on many occasions throughout the measurement campaign, most frequently during the morning rush hour. Based on the lack of organic aerosol processing (defined by the ratio of m/z = 44/57 in the Q-AMS spectra), strong correlation with NOx and CO, and a lack of significant increase in PWSOC concentration, the spikes in organic aerosol were likely associated with primary organic aerosol (POA). During these events, gas-phase HNO3 concentration decreases were observed simultaneously with increases in gas-phase HONO concentrations. These data likely indicate uptake of HNO3 and subsequent heterogeneous conversion to HONO involving POA. Preliminary calculations show that HNO3 partitioning could account for the majority of the observed HONO and aerosol nitrate concentrations during these events. Q-AMS chloride and HCl data also indicate uptake of chloride by particles during these events. This phenomenon was also observed during the night, but these nocturnal events were less

  18. S-2-amino-5-(2-nitroimidazol-1-yl)pentanoic acid: a model for potential bioreductively activated prodrugs for inhibitors of nitric oxide synthase (NOS) activity.

    Science.gov (United States)

    Ulhaq, S; Naylor, M A; Chinje, E C; Threadgill, M D; Stratford, I J

    1997-01-01

    Treatment of 1,1-dimethylethyl S-(2-1,1-dimethylethoxycarbonylamino)-5-bromopentanoate with 1-potassio-2-nitroimidazole, followed by deprotection, afforded S-2-amino-5-(2-nitroimidazol-1-yl)pentanoic acid, which was reduced to S-2-amino-5-(2-aminoimidazol-1-yl)pentanoic acid. This aminoimadazole inhibited rat brain nitric oxide synthase (NOS) activity 3.2 times more potently than did the nitro analogue. Thus S-2-amino-5-(2-nitroimidazol-1-yl)pentanoic acid is a potent prodrug which may be bioreductively activated to a NOS inhibitor in hypoxic solid tumours. PMID:9051114

  19. Role of central glutamate receptors, nitric oxide and soluble guanylyl cyclase in the inhibition by endotoxin of rat gastric acid secretion

    OpenAIRE

    García-Zaragozá, Eugenia; Barrachina, M Dolores; Moreno, Lucrecia; Esplugues, Juan V.

    2000-01-01

    This study examines the role of a central pathway involving glutamate receptors, nitric oxide (NO) and cyclic GMP in the acute inhibitory effects of low doses of peripheral endotoxin on pentagastrin-stimulated acid production.Vagotomy or intracisternal (i.c.) microinjections of the NO-inhibitor, NG-nitro-L-arginine methyl esther (L-NAME; 200 μg rat−1) restored acid secretory responses in endotoxin (10 μg kg−1, i.v.)-treated rats.The acid-inhibitory effect of i.v. endotoxin (10 μg kg−1, i.v.) ...

  20. Investigation of the direct and indirect electrochemical oxidation of hydrazine in nitric acid medium on platinum; Etude de l`oxydation electrochimique directe et indirecte de l`hydrazine en milieu acide nitrique sur platine

    Energy Technology Data Exchange (ETDEWEB)

    Cames, B

    1997-12-31

    In nuclear fuel processing by the PUREX process, the purification of plutonium in nitric acid medium requires the oxidation of Pu(III) to Pu(IV), and of hydrazinium nitrate to nitrogen. The study helped to characterize the electrochemical behavior of the oxidation of hydrazinium nitrate and the reduction of nitric acid to nitrous acid, a compound which can chemically oxidize hydrazinium nitrate and Pu(III). Electro-analytical studies on polycrystalline platinum showed that hydrazine is oxidized in two potential zones, which depend on the surface texture of the platinum anode. Electrolysis in separate compartments, carried out in medium-acid media (2 and 4 mo/l) in the potential zone where these processes take place, showed that, at 0.9 V/ECS, the hydrazine oxidation reactions involved are: a four-electron process (75 %) with nitrogen formation and a one-electron process (25 %) with formation of nitrogen and ammonium ion. By contrast, electrolysis carried out at 0.65 V/ECS (with reactivation of the electrode at - 0.2 V/ECS to remove the poison from the platinum) allowed the selective oxidation of hydrazine to nitrogen by the four-electron reaction. Nitric acid can only be reduced to nitrous acid in the absence of hydrazine. For medium-acid media ({<=} 6 mol/l), this reaction takes place at potentials below - 0.2 V/ECS. However, the production rate of nitrous acid (partial order 0 with respect to nitric acid) is very low compared with the values obtained for strongly-acid media (6 to 10 mol/l) at the potential of - 0.1 V/ECS. Note that, in concentrated nitric medium, the selectivity of the reduction reaction is 47 to 85 % for nitrous acid, depending on the nitric acid concentration (6 to 10 mol/l) and the potential imposed (- 0.1 {<=} E {<=} 0.6 V/ECS). A kinetic study helped to determine the hydrazine oxidation rates as a function of the operating conditions. In all cases, the reaction rate is of partial order 0 with respect to hydrazine. These studies accordingly