WorldWideScience

Sample records for phosphoric acid d2ehpa

  1. Liquid-liquid extraction of uranium from Egyptian phosphoric acid using a synergistic D2EHPA-DBBP mixture

    International Nuclear Information System (INIS)

    Abdel-Khalek, A.A.

    2011-01-01

    Extraction of uranium from Egyptian phosphoric acid with synergistic mixture of di-2-ethylhexylphosphoric acid (D2EHPA) and di-butyl butyl phosphonate (DBBP) is reported in this paper. The influence of various factors such as D2EHPA concentration, DBBP concentration, phosphoric acid concentration, contact time, aqueous: organic phase's ratio (aq:org) and temperature on the degree of extraction has been established. The data on the effect of temperature on the extraction showed that the enthalpy change is -23.12 kJ/mol. Uranium extracted by D2EHPA- DBBP is further subjected to a second cycle of extraction and scrubbing impurities. The uranium is finally converted to a high purity UO 3 product using precipitation with hydrogen peroxide and heat treatment at 375 deg C. (author)

  2. Kinetic studies on uranium stripping in D2EHPA+TBP/phosphoric acid system

    International Nuclear Information System (INIS)

    Yadav, K.K.; Singh, D.K.; Kotekar, M.K.; Anitha, M.; Vijayalakshmi, R.; Singh, H.

    2010-01-01

    Full text: A novel process based on synergistic mixture of 1.5 M D2EHPA (di 2 ethyl hexyl phosphoric acid) + 0.2 M TBP (tri-n-butyl phosphate) to recover uranium from wet process phosphoric acid (WPA) has been developed. Though the equilibrium study for the above process has been investigated in detail its kinetic behavior has not been reported so far. The work presented in the paper is an attempt to study the kinetics of U(VI) stripping from extractant phase to aqueous phase in a constant interfacial area cell (Lewis cell). Kinetic study of the solvent extraction process helps in designing of equipment and optimizing process condition for the better utilization of solvent inventory. Mass transfer kinetics of stripping of U(VI) from loaded 1.5M D2EHPA+ 0.2M TBP with phosphoric acid (AR) has been studied over a wide range of experimental conditions such as stirring speed, interfacial contact area, phosphoric acid concentration, uranium concentration, extractant concentration in organic phase and temperature. Investigation on effect of stirring speed (100-500 rpm) on stripping of U(VI) showed that the rate constant (k) values increases linearly with increase in stirring speeds from 100 to 300 rpm (0.03 to 0.075 cm/min), while the k values were almost constant (0.0819 cm/min) in 300 to 400 rpm range, beyond 450 rpm the k values again increased due to increased turbulence at the interface. The rate constant value (∼0.0814 cm/min) was found to be independent of interfacial contact area (24.6 to 67.02 cm 2 ) available for mass transfer. The rate constants were found to increase with increase in phosphoric acid concentration (6-10M) and temperature (30-60 deg C), the values being in the range of 0.01 to 0.082 cm/min. The slopes of ln-ln plot showed that the stripping of U(VI) has a second order dependence on phosphoric acid concentration (slope∼2) at temperatures ranging from 30 to 60 deg C. The activation energy value for uranium stripping was found to be in the

  3. Developing a rapid method for the determination of uranium in pure phosphoric acid and D2 EHPA

    International Nuclear Information System (INIS)

    Koudsi, Y.; Stas, J.; Al-Merey, R.; shaddoud, G.

    1996-02-01

    Arsenazo (III) used in titrate uranium spectrophotometrically in phosphoric acid after its extraction into organic phase. In this work we used arsenazo(III) to complex uranyl ion in pure phosphoric acid and in the aqueous phase. The spectrum of the complex shows that λ max is at 650 nm. The linearity of the method is corelated with acid molarity, it is (1 -4, 10 - 30, 10 - 40) ppm uranium for (0.2, 1, 2) M of phosphoric acid respectively. Uranium in D 2 EHPA stripped by phosphoric acid and then determined by this method. Also it has been applied to determine uranium in pure perchloric acid. The method is direct, rapid, very cheap and relatively accurate. (author)

  4. Laboratory and pilot plant studies for the recovery of uranium from phosphoric acid by the D2EHPA-TOPO process

    International Nuclear Information System (INIS)

    Botella, T.; Gasos, P.

    1989-01-01

    The activities and costs involved in laboratory and pilot plant studies are discussed as applied to the D2EHPA-TOPO process. The overall capital investment (including engineering) for a plant with a throughput of 12 cubic meters of acid/day has been estimated to be around one million US dollars. Operating costs per year, without considering amortization and labor, are over 20,000 US dollars. A total time of 3,5 years (including engineering, purchase and pilot plant tests) could be needed to obtain the information required for final scale-up. (author). 40 refs, 1 fig., 5 tabs

  5. Liquid-liquid extraction (LLE) of Fe(III) and Ti(IV) by bis-(2-ethyl-hexyl) phosphoric acid (D2EHPA) in sulfuric acid medium; Extracao liquido-liquido de ferro (III) e titanio (IV) pelo acido bis-(2-etil-hexil) fosforico (D2EHPA) em meio de acido sulfurico

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Glauco Correa da; Cunha, Jose Waldemar Silva Dias da [Instituto de Engenharia Nuclear (IEN), Rio de Janeiro, RJ (Brazil). Dept. de Quimica e Materiais Nucleares; Dweck, Jo [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Escola de Quimica. Dept. de Processos Inorganicos; Afonso, Julio Carlos [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Inst. de Quimica. Dept. de Quimica Analitica]. E-mail: julio@iq.ufrj.br

    2008-07-01

    This work presents a study on the separation of Fe(III) and Ti(IV) from sulfuric acid leaching solutions of ilmenite (FeTiO{sub 3}) using liquid-liquid extraction with D2EHPA in n-dodecane as extracting agent. The distribution coefficients (K{sub D}) of the elements related to free acidity and concentration of Fe(III) and Ti(IV) were determined. Free acidity was changed from 3x10{sup -2} to 11.88 mol L{sup -1} and D2EHPA concentration was fixed at 1.5 mol L{sup 1}. Recovery of final products as well as recycling of wastes generated in the process were also investigated. The LLE process as a feasible alternative to obtain high-purity TiO{sub 2}. (author)

  6. Properties and synthesis of D2EHPA and of alkylphosphoric acid

    International Nuclear Information System (INIS)

    Elias, Abdelhamid

    1996-07-01

    A great interest has been devoted to alkylphosphates which are used in various field of chemical industry as: agents for extracting metals (uranium, actinides and lanthanides), flame-retardant solid plasticizers for cellulose acetate,cellulose ethers and vinyls,ignition control agents for gasoline, lubricant additive,antifoam agents for water-based paints and in inks and paper manufacture. In this context, the present work is achieved in order to supply a selected bibliography and the main theoretical aspects concerning physical and chemical properties, analysis techniques, synthesis and purification processes and some applications of D2EHPA (di(2-ethylhexyl)phosphoric acid or di(2-ethylhexyl)phosphate) and of alkylphosphates in general

  7. Extração líquido-líquido de ferro(III e titânio(IV pelo ácido bis-(2-etil-hexil fosfórico (D2EHPA em meio de ácido sulfúrico Liquid-liquid extraction (LLE of Fe(III and Ti(IV by bis-(2-ethyl-hexyl phosphoric acid (D2EHPA in sulfuric acid medium

    Directory of Open Access Journals (Sweden)

    Glauco Corrêa da Silva

    2008-01-01

    Full Text Available This work presents a study on the separation of Fe(III and Ti(IV from sulfuric acid leaching solutions of ilmenite (FeTiO3 using liquid-liquid extraction with D2EHPA in n-dodecane as extracting agent. The distribution coefficients (K D of the elements related to free acidity and concentration of Fe(III and Ti(IV were determined. Free acidity was changed from 3x10-2 to 11.88 mol L-1 and D2EHPA concentration was fixed at 1.5 mol L-1. Recovery of final products as well as recycling of wastes generated in the process were also investigated. The LLE process as a feasible alternative to obtain high-purity TiO2.

  8. Indium recovery from acidic aqueous solutions by solvent extraction with D2EHPA: a statistical approach to the experimental design

    Directory of Open Access Journals (Sweden)

    Fortes M.C.B.

    2003-01-01

    Full Text Available This experimental work presents the optimization results of obtaining a high indium concentration solution and minimum iron poisoning by solvent extraction with D2EHPA solubilized in isoparaffin and exxsol. The variables studied in the extraction step were D2EHPA concentration, acidity of the aqueous phase and time of contact between phases. Different hydrochloric and sulfuric acid concentrations were studied for the stripping step. The optimum experimental conditions resulted in a solution with 99% indium extraction and less than 4% iron. The construction of a McCabe-Thiele diagram indicated two theoretical countercurrent stages for indium extraction and at least six stages for indium stripping. Finally, the influence of associated metals found in typical sulfate leach liquors from zinc plants was studied. Under the experimental conditions for maximum indium extraction, 96% indium extraction was obtained, iron extraction was about 4% and no Ga, Cu and Zn were co-extracted.

  9. Uranium reextraction from D2EHPA-TOPO solvent

    International Nuclear Information System (INIS)

    Duarte Neto, J.

    1985-01-01

    A comparative study for recovering uranium from the solvent D 2 EHPA-TOPO (di-2-ethyl hexyl phosphoric acid - tri-n-octyl phosphine oxide) with ammonium carbonate and sodium carbonate solutions has been made. The paper discusses the precipitation of iron during stripping and the extracctant solubilization in the aqueous phases. Continuous tests showed that uranium is efficiently stripped from the solvent by using both solutions and that the choice of a specific system is dependent on the uranium precipitation mechanism to be employed. (Author) [pt

  10. The nature of Pu(IV) complex extracted by D2EHPA - A structure evaluation (Preprint No. AL.22)

    International Nuclear Information System (INIS)

    Phal, D.G.; Kannan, S.; Ramakrishna, V.V.

    1989-01-01

    To find out the composition of the Pu(IV) species extracted from sulphuric acid medium by di-2, ethyl hexyl phosphoric acid (D2EHPA) taken in any of the three diluents dodecane, toluene or chloroform and the changes in the composition of the extracted specis brought out by changing the aqueous medium from sulphuric to nitric acid as well as by the addition of thenoyltifluoroacetone (HTTA) to the organic phase were investigated and the results are reported here. (author)

  11. Investigation on the efficience precipitation of uranium from kerosene solution of 2-di-ethylhexylphosphoric acid (D2EHPA) + TOPO after 2rd extraction process

    International Nuclear Information System (INIS)

    Misiak, R.; Tlalka, M.

    1985-01-01

    The model extraction systems: D2EHPA + TOPO + U(6) + kerosene -(NH 4 ) 2 CO 3 were examined on creation of the emulsion. The stability of the primary emulsions, dispersion type and the time of living were determined. Filtration possibilities under atmospheric and low pressure on ammonium-uranyl carbonate were investigated. The influence of temperature on velocity separation of the emulsion and the kinetics of stripping of uranium was given. Colorimetric method has been used for determination yield of the uranium. 2 refs., 8 figs. (author)

  12. The separation of U and Y by D2EHPA

    International Nuclear Information System (INIS)

    Dwi-Biyantoro; Subagiono, R.; Rosyidin; Kris-Tri-Basuki; Tri-Handini; Purwoto

    1996-01-01

    The separation of uranium and yttrium in hydrochloric acid was extracted by D 2 EHPA in dodecane. This process used liquid-liquid extraction method. The variables studied were the concentration of hydrochloric acid, the concentration of extractant, time of extraction, and the temperature of extraction. The data evaluation of the research showed that the optimum condition was as follows: the concentration of HCI = 0.2 M, the concentration of extractant = 0.15 M D 2 EHPA, the time of extraction = 15 minutes, and the temperature of extraction = 20 o C. It was found that the distribution coefficient of uranium was = 34.43, the distribution coefficient of yttrium was = 2.20, and the separation factor of U-Y= 15.65

  13. Few studies of the effect of diluents on extraction of cobalt with D2EHPA. D2EHPA ni yoru Co no chushutsu ni ataeru kishakuzai no eikyo ni kansuru jakkan no kento

    Energy Technology Data Exchange (ETDEWEB)

    Aranae, M.; Nakataka, Y.; Wakamatsu, T. (Kyoto Univ., Kyoto (Japan). Faculty of Engineering); Saito, I.; Sakamoto, H. (Environment Research Inst. Resources Technical Tsukuba (Japan))

    1991-12-27

    Study was made on extraction of cobalt from weak acid solution with di-(2-ethylhexyl) phosphoric acid (D2EHPA) using various polar diluents such as benzene, toluene, o-xylene, m-xylene, n-heptane, cyclohexane and n-hepatne-benzene mixtures. Extraction efficiency of cobalt has decreased in the order, n-heptane > cyclohexane > m-xylene > o-xylene > toluene > benzene and this order has been in good agreement with the decreasing order of solubility parameters of diluents,and has shown the possibility of application of regular solution theory. When n-heptane and cyclohexane as diluents, in low loading ratio(L),were used Co-D2EHPA polymer were formed compared to other diluents. On the other hand when mixture of n-heptane/benzene was used as diluent, the efficiency of extraction, salting-out effect and formation of Co-D2EHPA polymer has changed with the texture of mixture.This change may be due to the effect of L and it has been thought for the necessity of investigation of extraction of cobalt in low polar diluents. 13 refs., 5 figs., 2 tabs.

  14. Direct determination of uranium in the organic phase D2EHPA-TOPO using XRF spectroscopy

    International Nuclear Information System (INIS)

    Stas, J.; Al-Merey, R.; Karajo, J.

    2000-06-01

    Three calibration curves have been carried out to determine uranium concentration in the organic phase (D2EHPA-TOPO) using XRF technique with Cd 109 as a primary exciting source. Copper was used as an internal standard, so the linear relation between relative intensity of uranium against its concentration has been obtained. The range of uranium concentrations studies are (0-100 μg.mL -1 ), (100-1000 μg.mL -1 ) and (1000-6500 μg.mL -1 ), which covered all uranium against its concentration concerning first and second cycles of uranium extraction from phosphoric acid. detection limit was found to be 1.1 μg/ml. The effect of different range of (0.2-0.6 M) D2EHPA and (0.025-0.15 M) TOPO and iron (0-500 μg.mL -1 ) on the accuracy and the precision of uranium determination have been studied and no effect was found. Unknown organic samples have been analyzed using XRF technique and compared with γ-ray, UV and volumetric techniques, obtained results were comparable. (Author)

  15. Separation of yttrium using carbon nanotube doped polymeric beads impregnated with D2EHPA

    International Nuclear Information System (INIS)

    Dasgupta, Kinshuk; Yadav, Kartikey K.; Singh, D.K.; Anitha, M.; Singh, H.

    2013-01-01

    Di-2-ethylhexyl phosphoric acid impregnated polyethersulfone based composite beads in combination with additives such as polyvinyl alcohol (PVA) and multiwalled carbon nanotube (MWCNT) has been prepared by non-solvent phase inversion method. The synthesized beads were characterized by scanning electron microscopy, thermogravimetry and infra-red spectroscopy. Effect of additives on bead morphology, solvent impregnation capacity, extractability and stability has been examined to compare their suitability for yttrium recovery from acidic medium. Microstructural investigation as well as experimental findings confirmed the role of additives in modifying the pore structures in beads, responsible for varied degree of yttrium extraction. Further the role of metal ion concentration in aqueous phase on its recovery by polymeric beads was also evaluated. Among the tested beads PES/D2EHPA/MWCNT/PVA beads were found to be superior for Y(Ill) extraction. (author)

  16. Method for recovery of uranium from phosphoric acid

    International Nuclear Information System (INIS)

    Duarte Neto, J.

    1984-01-01

    The results of a method for recuperation of uranium from phosphoric acid by humid way are presented. The extracting mixture used was di-ethylhexylphosphoric acid (D 2 EHPA) and trioctylphosphine oxide (TOPO). An installation in micro-pilot scale was made to get and visualize data for continuous process. (M.A.C.) [pt

  17. Solvent Extraction of Rare Earths by Di-2 Ethylhexyl Phosphoric Acid

    International Nuclear Information System (INIS)

    Srinuttrakul, Wannee; Kranlert, Kannika; Kraikaew, Jarunee; Pongpansook, Surasak; Chayavadhanangkur, Chavalek; Kranlert, Kannika

    2004-10-01

    Solvent extraction has been widely applied for individual rare earth separation because the separation time is rapid and a large quantity of products is obtained. In this work, this technique was utilized to extract mixed rare earths, obtained from monazite digestion process. Di-2-ethylhexyl phosphoric acid (D2EHPA) was used as an extractant. The factors affected the extraction including HNO 3 concentration in mixed rare earth nitrate solution and the amount of D2EHPA were studied. The appropriate concentrations of HNO 3 and D2EHPA were found to be 0.01 and 1.5 M, respectively. From the result of equilibrium curve study, it was observed that heavy rare earths were extracted more efficient than light rare earths. A 6-stage continuous countercurrent solvent extraction was simulated for rare earth extraction. The optimum ratio of solvent to feed solution (S/F) was 2. Because of the high cost of D2EHPA, 1.0 M of D2EHPA was suitable for the rare earth extraction by the continuous countercurrent solvent extraction

  18. Batch Simulation of Rare Earths Extractive Separation by Di (2-Ethylhexyl) Phosphoric Acid and Tributylphosphate in Kerosene

    International Nuclear Information System (INIS)

    Kraikaew, Jarunee; Srinuttakul, Wanee

    2004-01-01

    Liquid-liquid extraction is applied to separate individual rare earths. In this research, 6-stage continuous countercurrent solvent extraction was simulated to extract rare earths from rare earth nitrate solution, which was obtained from monazite processing, to estimate the possible optimum operating conditions for pilot or industrial plants. The solvent(S) per feed(F) ratio (S/F) was varied from 1 to 3. The organic are 1.0 and 1.5 Molars (M) Di (2-ethylhexyl) phosphoric acid (D2EHPA) in kerosene. 50% tributylphosphate (TBP) in kerosene was applied for comparison. It was found that D2EHPA was a good extracting agent for heavy rare earths while TBP extracted well both light and heavy rare earths. After extraction with TBP and D2EHPA, the extraction efficiency at solvent per feed ratio (S/F) =2 and 3 showed a slight difference. S/F =2 was selected commercially for operation

  19. Flotation of uranium values using di (2-ethyl hexyl) phosphoric acid

    International Nuclear Information System (INIS)

    Singh, Ajoy Kumar; Padmanabhan, N.P.H.; Sridhar, U.; Krishna Rao, N.

    1998-01-01

    The use of solvent extractants for mineral flotation, especially for difficult-to-float minerals, is gaining importance as they are highly selective to specific metal ions and form strong and stable complexes mostly by chelation. Studies carried out with di(2 ethyl hexyl) phosphoric acid (D2EHPA) (an organic solvent used in the extraction of uranium from phosphoric acid) as collector for flotation of uranium minerals from ore samples of Domiasiat, Meghalaya and Jaduguda, Bihar have yielded encouraging results. Although flotation of uranium minerals using other solvent extractants like tributyl phosphoric acid (TBP) has been studied, the uraninite-D2EHPA system has not been tested so far. This technical note puts on record the findings of the preliminary studies carried out. (author)

  20. Extractive separation of Al(III) and Ni(II) by Di-2-Ethylhexyl phosphoric acid-kerosene system from aqueous fluoride medium

    International Nuclear Information System (INIS)

    Islam, M.F.; Begum, D.A.; Rahman, M.; Rahman, M.S.

    2009-01-01

    In the study of the extractive separation of Al(III) and Ni(II) by di-2-ethylhexyl phosphoric acid D2EHPA-kerosene from aqueous fluoride medium, about 94% Al(III) and 2% Ni(II) were extracted with 0.3 M D2EHPA (pH 2.1 and temperature 30+-1 degree C). Extraction of Ni(II) decreased with increasing extractant concentration. D2EHPA-kerosene-fluoride system showed better extraction of Al(III) with higher extractant concentration and aqueous pH and vice versa for the extraction of Ni(II). The maximum separation factor (beta 1380) was obtained for Al(III) at 20 degree C and decreased to (beta 732) at 60 degree C. The separation of Al(III) from Ni(II) was favoured at normal temperature. Extraction followed the order Al(III), Ni(II). About 99% stripping of Al(III) was attained from the loaded 0.20 M D2EHPA. Much faster extraction of Al(III) compared to Ni(II) and preferential loading were shown by D2EHPA-kerosene in the presence of fluoride ion in the aqueous phase. Separation of Al(III) was the most outstanding from Ni-Al-F-complex solution. (author)

  1. Semitechnical studies of uranium recovery from wet process phosphoric acid by liquid-liquid-extraction method

    International Nuclear Information System (INIS)

    Poczynajlo, A.; Wlodarski, R.; Giers, M.

    1987-01-01

    A semitechnical installation for uranium recovery from wet process phosphoric acid has been built. The installation is based on technological process comprising 2 extraction cycles, the first with a mixture of mono- and dinonylphenylphosphoric acids (NPPA) and the second with a synergic mixture of di-/2-ethylhexyl/-phosphoric acid (D2EHPA) and trioctylphosphine oxide (TOPO). The installation was set going and the studies on the concentration distributions of uranium and other components of phosphoric acid have been performed for all technological circuits. 23 refs., 15 figs., 3 tabs. (author)

  2. Extraction studies on rare earths using dinonyl phenyl phosphoric acid

    International Nuclear Information System (INIS)

    Anitha, M.; Singh, D.K.; Kotekar, M.K.; Vijayalakshmi, R.; Singh, H.

    2011-01-01

    Rare earths are widely used in phosphor materials, magnetic substances, alloys, catalyst, lasers, superconductors, solid oxide fuel cells and in nuclear applications. The high value of these elements depends on their effective separation into high purity compounds. The separation into individual rare earths is very difficult to achieve, due to the very low separation factors between two adjacent rare earths arising due to similar chemical properties. Taking the advantage of variation in basicity, the separation is generally accomplished by solvent extraction or ion exchange. There are several references on the separation of rare earth in different media employing various types of extractants such as 2-ethylhexyl 2-ethyhexylphosphonic acid (EHEHPA) and di-2-ethyl hexyl phosphoric acid (D2EHPA) which have been widely used for the separation and purification of rare earths. Dinonyl phenyl phosphoric acid (DNPPA) is an organo phosphorus extractant (pKa = 2.54) and is an aromatic analogue of D2EHPA, which extracts metal ion by cation exchange mechanism. DNPPA was explored to recover rare earths from phosphate media such as wet process phosphoric acid and merchant grade acid. However, there is no information available in literature on DNPPA for RE extraction from chloride medium. Therefore, an attempt has been made in the present study to investigate the feasibility of using DNPPA for extraction of La(III), Dy(III) and Y(III) from chloride medium

  3. Development of an improved two-cycle process for recovering uranium from wet-process phosphoric acid

    International Nuclear Information System (INIS)

    Chen, H.M.; Chen, H.J.; Tsai, Y.M.; Lee, T.W.; Ting, G.

    1987-01-01

    An improved two-cycle separation process for the recovery of uranium from wet-process phosphoric acid by extraction with bis(2-ethylhexyl)phosphoric acid (D2EHPA) plus dibutyl butylphosphonate (DBBP) in kerosene has been developed and demonstrated successfully in bench-scale, continuous mixer-settler tests. The sulfuric acid and water scrubbing steps for the recycled extraction in the second cycle solve the problems of the contamination and dilution of the phosphoric acid by the ammonium ion and water and also avoid the formation of undesirable phosphatic precipitates during the subsequent extraction of uranium by recycled organic extractant

  4. Novel D2EHPA-polysiloxane-based sorbent for titanium (IV) extraction and separation

    International Nuclear Information System (INIS)

    Mendoza R, L. G.; Rodriguez de San Miguel, E.; Pardo G, D. Y.; De Gyves, J.; Sanchez G, J. P.

    2011-01-01

    In this work the synthesis, characterization and evaluation of a novel sorbent material used for the solid-phase extraction of titanium (IV) from hydrochloric acid medium is described. The material was prepared by the sol-gel route incorporating bis(2-ethylhexyl phosporic acid) (D2EHPA) as extractant within a polymeric matrix based on polysiloxanes and characterized through Ftir-Atr, XRD, 29 Si and 31 P NMR, TGA and DSC. In studies of titanium sorption and desorption in batch mode several factors related with the extraction and back-extraction operations were evaluated, such as: contact time, titanium concentration, nature and composition of the aqueous media, and extractant concentration in the sorbent. The maximum sorption was observed at 30 min of contact time in a 1 mol L -1 HCl + 0.1% KCl medium, while the maximum desorption was observed at 60 min in a 1.5 mol L -1 H 2 SO 4 + 20% v/v H 2 O 2 medium when titanium concentration was 70 mg L -1 . Under optimal conditions the recovered percent of titanium was nearly 90%. In addition, the characterization of the extraction equilibrium was performed. The selectivity of the method was studied adding Al(III), Fe(III) and V(v) to the extraction medium. A high selectivity for Ti over Al and Fe was observed, even at high concentrations of the interferences; 50% of Ti, only 7% of Fe, 3% of Al and less than 1% of V were recovered under the established conditions. The method was finally applied for titanium recovery from a certified fly ash sample generated from a municipal incineration plant. (Author)

  5. Novel D2EHPA-polysiloxane-based sorbent for titanium (IV) extraction and separation

    Energy Technology Data Exchange (ETDEWEB)

    Mendoza R, L. G.; Rodriguez de San Miguel, E.; Pardo G, D. Y.; De Gyves, J. [UNAM, Facultad de Quimica, Departamento de Quimica Analitica, Ciudad Universitaria, 04510 Mexico D. F. (Mexico); Sanchez G, J. P., E-mail: degyves@unam.mx [Instituto Mexicano del Petroleo, Laboratorio de Evaluacion Molecular, Eje Central Norte Lazaro Cardenas No. 152, Apdo. Postal 14-805, 07730 Mexico D. F. (Mexico)

    2011-07-01

    In this work the synthesis, characterization and evaluation of a novel sorbent material used for the solid-phase extraction of titanium (IV) from hydrochloric acid medium is described. The material was prepared by the sol-gel route incorporating bis(2-ethylhexyl phosporic acid) (D2EHPA) as extractant within a polymeric matrix based on polysiloxanes and characterized through Ftir-Atr, XRD, {sup 29}Si and {sup 31}P NMR, TGA and DSC. In studies of titanium sorption and desorption in batch mode several factors related with the extraction and back-extraction operations were evaluated, such as: contact time, titanium concentration, nature and composition of the aqueous media, and extractant concentration in the sorbent. The maximum sorption was observed at 30 min of contact time in a 1 mol L{sup -1} HCl + 0.1% KCl medium, while the maximum desorption was observed at 60 min in a 1.5 mol L{sup -1} H{sub 2}SO{sub 4} + 20% v/v H{sub 2}O{sub 2} medium when titanium concentration was 70 mg L{sup -1}. Under optimal conditions the recovered percent of titanium was nearly 90%. In addition, the characterization of the extraction equilibrium was performed. The selectivity of the method was studied adding Al(III), Fe(III) and V(v) to the extraction medium. A high selectivity for Ti over Al and Fe was observed, even at high concentrations of the interferences; 50% of Ti, only 7% of Fe, 3% of Al and less than 1% of V were recovered under the established conditions. The method was finally applied for titanium recovery from a certified fly ash sample generated from a municipal incineration plant. (Author)

  6. Solvent extraction of Zn(II) from aqueous sulphate media by di(2-ethylhexyl) phosphoric acid in kerosene

    International Nuclear Information System (INIS)

    Begum, D.A.; Alauddin, M.; Rahman, M.S.

    2009-01-01

    The extraction equilibrium studies of Zn(II) from sulphate medium by di(2-ethylhexyl) phosphoric acid (D2EHPA, H/sub 2/A/sub 2/) in kerosene revealed that the distribution ratio (D) decreased with the increase of initial (Zn(A(II) in the aqueous phase and increased with the increase of equilibrium pH and extractant concentration. The equilibration is reached within 2 min. The species extracted into the organic phase is thought to be ZnA2, HA. The pH and extractant dependencies were about 2 and 1.67, respectively. The distribution ratio decreased with the increase in sulphate ion concentration in the aqueous phase. The extraction equilibrium reaction is suggested as Zn/sup 2+/ /sub aq/ +1.5 (H/sub 2/A/sub 2/)org - (ZnA/sub 2/, HA)org +2H/sup +/ /sub aq/. The extraction equilibrium constant (kex) for the above reaction was calculated to be 10-2.26. The extraction process was endothermic in nature having positive DH value of 16.27 kJ/mol. The loading of D2EHPA by Zn(II) is about 4.50 g of Zn(II) by 0.10 M D2EHPA. Possible reaction mechanism has been suggested based on distribution data, extractant concentration and equilibrium pH of the aqueous phase. (author)

  7. Recuperation of uranium from phosphoric acid

    International Nuclear Information System (INIS)

    Cordero, G.; Jodra, L.G.; Otero, J.L.; Josa, J.M.

    1977-01-01

    The Spanish capacity for phosphoric acid production is 500.000 t P 2 O 5 /yr. This acid has an average concentration of 365 g U 3 O 8 / t P 2 O 5 . Therefore about 180 t U 3 O 8 /yr are dissolved. In 1969, the Junta de Energia Nuclear (JEN) developed, in bench scale, a solvent extraction process to recover the uranium from the phosphoric acid. The solvent used was a synergistic mixture of D2EHPA and TOPO. The results were very promising with good recovery and very high quality for the uranium concentrate. Later, the J.E.N. continued the studies in a pilot plant scale. For this purpose, was built an experimental facility in Huelva; it can treat about 7 cu. m/day of brown acid. Fosforico Espanol, S.A. (FESA) collaborated in the studies and agreed to setting up these installations in their factory. They also provided fresh phosphoric acid for the tests. In this pilot plant we studied the following stages: a) Clarification and conditioning of the phosphoric acid; b) Uranium extraction followed by stripping in a reducing medium; c) Purification by extraction and washing; d) Obtention of the concentrate by stripping with ammonia and CO 2 gas, followed by crystallization of the ammonium uranyl tricarbonate (AUT); and e) Calcination of the concentrate to decompose the AUT to uranium oxides. The results confirmed the laboratory test data. Recuperation levels were between 85 and 90%. The AUT calcined at 550 0 C. gave a product with 96-98% U 3 O 8 . In view of the pilot plant results we have prepared a black book for an industrial plant to treat about 3700 cu. m/day of phosphoric acid. At the present time the financial aspects of this installation are being studied [es

  8. Permeabilitas Membran Transpor Campuran Unsur Tanah Jarang (La, Nd, Gd, Lu Menggunakan Carrier (TBP : D2EHPA Melalui Supported Liquid Membrane

    Directory of Open Access Journals (Sweden)

    Djabal Nur Basir

    2015-01-01

    Full Text Available Methods that have been developed currently for the separation and purification of rare earth elements, REE’s are solvent extraction by through immobilization of an extracting agent in a porous polymeric membrane. This methods beside could increase the transport selectivity, also the amount of carrier was very few. This technique is known as supported liquid membrane, SLM. Research toward transport and separation of REE’s through SLM have been still relatively limited merely to single feed-binary mixture, and one type of carrier. The transport   membrane permeability was obtained in a mixture of REE’s (La,Nd,Gd,Lu using the carrier TBP : D2EHPA by SLM. In this SLM technique, supporting membrane PTFE (polytetrafluoroethylene was soaked in a mixture of TBP carrier (tributilfosfat as a neutral ligand and D2EHPA (acid-2- etilheksilfosfat as anionic ligand with a particular concentration ratio in the solvent kerosene as membrane phase. HCl as receiver phase and solution mixture of REE’s as feed phase. Determination of the REE’s total concentration was carried out by UV-Vis spectrophotometry with NAS (sodium alizarin sulfonate as the colouring agent at pH 4,75 and the solution absorbance was determinated at 534 nm as maximum wavelength. Transport patterns of REE’s on the variation of the concentration of total mixed carrier composition, pH, and concentration  of the receiver phase were done for 300 minutes. The optimum conditions of transport mixture of REE’s (La, Nd, Gd, Lu were feed phase pH 3,0; carrier TBP: D2EHPA (0,3:0,7 M; and receiver phase HCl 3,0 M. In this condition, the transport membrane permeability in mixture of REE’s was 0,1077 cm.menit-1 with the percent of transport was 95,24%.

  9. Investigation of the synergic effect of some neutral organophosphoric compounds on the extraction of uranium from phosphoric acid solutions by D1-(2-Ethyl Hexyl) phosphoric acid

    International Nuclear Information System (INIS)

    Stas, J.; Khorfan, S.; Koudsi, Y.

    1998-05-01

    The extraction of uranium (VI) from pure phosphoric acid media by D2EHPA/Kerosene has been studied. The mechanism of the extraction was found as follows: The logarithm of the equilibrium constant of the extraction (LogKex) was found (3.06), (3.32), (3.24), (3.3) for the following phosphoric acid concentrations respectively (1), (2), (3), (4) Mol/1, and the enthalpy change DELTA H was found (-100.68 kj/mol). (-76 kj/mol) for (1), (2) mol/1 phosphoric acid concentrations. The synergic effect of TOPO, TBP, and TBPI with DEHPA have been studied during the extraction of uranium from pure phosphoric acid and Syrian commercial phosphoric acid. The synergic effect increases as follows: TBP< TBPI<< TOPO (In pure phosphoric acid), TBPI approx TBP<< TOPO (In Syrian commercial phosphoric acid). The difficulty of extracting uranium (VI) from Syrian commercial phosphoric acid in comparison with pure phosphoric acid is due to the presence of several impurities capable of complexing uranium, and a small amounts of solid and organic matters, all these are factors which reduce the distribution coefficient of uranium. (Author)

  10. Uranium recovery from the concentrated phosphoric acid prepared by the hemi-hydrate process

    Energy Technology Data Exchange (ETDEWEB)

    Fouad, E A; Mahdy, M A; Bakr, M Y [Nuclear materials authority, Cairo, (Egypt); Zatout, A A [Faculty of engineering, Alex. university, Alex, (Egypt)

    1995-10-01

    It has been proved that the uranium dissolution from El-sebaiya phosphate ore was possible by using 10 Kg of K Cl O{sub 4}/ ton rock during the preparation of high strength phosphoric acid using the hemi hydrate process. In the present work, effective extraction of uranium (about 90%) from the high strength phosphoric acid using a new synergistic solvent mixture of 0.75 M D 2 EHPA/0.1 M TOHPO had been a success. Stripping of uranium from the organic phase was possible by 10 M phosphoric acid while the direct precipitation of uranium concentrate from the later was feasible by using N H{sub 4} F in presence of acetone. 8 figs.

  11. Uranium recovery from the concentrated phosphoric acid prepared by the hemi-hydrate process

    International Nuclear Information System (INIS)

    Fouad, E.A.; Mahdy, M.A.; Bakr, M.Y.; Zatout, A.A.

    1995-01-01

    It has been proved that the uranium dissolution from El-sebaiya phosphate ore was possible by using 10 Kg of K Cl O 4 / ton rock during the preparation of high strength phosphoric acid using the hemi hydrate process. In the present work, effective extraction of uranium (about 90%) from the high strength phosphoric acid using a new synergistic solvent mixture of 0.75 M D 2 EHPA/0.1 M TOHPO had been a success. Stripping of uranium from the organic phase was possible by 10 M phosphoric acid while the direct precipitation of uranium concentrate from the later was feasible by using N H 4 F in presence of acetone. 8 figs

  12. The extraction of zinc and other minor metals from concentrated ammonium chloride solutions with D2EHPA and Cyanex 272

    Directory of Open Access Journals (Sweden)

    Amer, S.

    1995-12-01

    Full Text Available A comparative study is made of the extractants D2EHPA and Cyanex 272 for the zinc and minor metal extraction from aqueous concentrated ammonium chloride solutions, as those of the leaching liquors of the CENIM-LNETI process. Extraction equilibrium data for zinc are presented as extraction isotherms at constant pH and at a temperature of 50 °C. Zinc extraction and coextraction of minor metal ions as Cu, Ca, Pb, Mg, Cd, Co, Ni and Hg are studied. Mercury does not extract from concentrated ammonium chloride solutions. Cyanex 272 shows a better selectivity for zinc with regard to the minor metals than D2EHPA, which is especially remarkable for calcium, the most coextracted element by D2EHPA. Nickel and cadmium coextraction is negligible for both extractants. The possible use of the Cyanex 272 as an alternative to D2EHPA is considered.

    Se realiza un estudio comparativo del comportamiento del D2EHPA y del Cyanex 272 durante la extracción del cinc y otros metales minoritarios de soluciones acuosas concentradas de cloruro amónico, como las de las soluciones de lixiviación del proceso CENIM-LNETI. Se presentan los datos de equilibrio de extracción del cinc en forma de isotermas de extracción a una temperatura de 50 °C y pH constante y se estudia la coextracción de los metales minoritarios Cu, Ca, Pb, Mg, Cd, Co, Ni y Hg. El mercurio no se extrae de las soluciones concentradas de cloruro amónico. La selectividad del Cyanex 272 para el cinc respecto de esos metales minoritarios es mejor que la del D2EHPA, siendo verdaderamente notable para el calcio, que es la impureza que más se coextrae con el D2EHPA. La coextracción de níquel y de cadmio es muy pequeña para ambos extractantes. Se considera la posibilidad del uso alternativo del Cyanex 272 en lugar del D2EHPA.

  13. Gas chromatographic analysis of Tri-N-Octyl-Phosphine oxide (Topo) in D2EHPA-Topo-Kerosene mixtures

    International Nuclear Information System (INIS)

    Perez Garcia, M.

    1973-01-01

    A study about the minimum limit of TOPO, detectable by gas chromatography in an organic phase formed by D2EHPA and kerosene is carried out. The retention time and response factor under the same conditions are also studied. Octacosane has been used as a reference hydrocarbon. (Author) 8 refs

  14. Synergistic extraction of gold from sulfuric acid solution containing thiourea. Ryusan sansei chio nyoso yoeki kara no kin no kyodo chushutsu

    Energy Technology Data Exchange (ETDEWEB)

    Niinae, M.; Nakahiro, Y.; Wakamatsu, T. (Kyoto Univ., Kyoto (Japan). Faculty of Engineering); Oboso, A. (Kyoto Univ., Kyoto (Japan). Graduate School); Takenaka, Y. (Kyoto Univ., Kyoto (Japan))

    1991-08-20

    Solvent extraction was investigated as a method of recovering Au from sulfuric acid solution containing thiourea. With the objective of improving Au extraction by die-(2-ethylhexyl) phosphoric acid (D2EHPA) and tri-n-octylamine (TOA), effects of D2EHPA, TOA, TBP (tri-n-butyl phosphate), and trioctyl phosphine oxide (TOPO) as extractants were investigated. When mixed extractant of D2EHPA with TBP or TOPO, or mixture of TOA with TBP or TOPO was used, synergistic effect was observed for the extraction of AU, and they were proved to be effective for the improvement of Au extraction. When D2EHPA/TBP and D2EHPA/TOPO mixtures were used, the extraction of Fe was suppressed on the contrary, and they were found to be effective for the separation of Au and Fe. Benzene used as diluent seemed to be favorable to both the extraction of Au and the separation of Au and Fe. The selection of sulfuric acid concentration seemed to be an important factor for the extraction efficiency of Au and the separation efficiency of Au and Fe, while little effect was observed with the concentration of thiourea. 4 refs., 8 figs., 4 tabs.

  15. Separation of zirconium (Zr) and hafnium (Hf) using solvent mixture of TBP-D_2EHPA and amberlite XAD-16

    International Nuclear Information System (INIS)

    Dwi Biyantoro; I Made Sukarna; Agus Suyanto

    2017-01-01

    The aims of this research were to determine the composition (ratio of extractant and resin) of the SIR which is effective for the separation of Zr and Hf, knowing adsorption equilibrium models Zr and Hf using the SIR, and knowing the most effective adsorption results from SIR weight ratio. The research was conducted by using the SIR method that is impregnating the extractant into the resin. Extractant used is a mixture of TBP and D_2EHPA (1 : 3), the resin used is XAD-16, and the feed used is ZOC. This research was conducted by varying the composition of the SIR, after the result of effective SIR variation. Adsorption process is then performed using the ZOC with SIR. Then filtered, the filtrate was analyzed by XRF. While solids SIR adsorption product was desorbed using sulfuric acid. Then the desorption results were analyzed using XRF spectrometer. Based on calculations, the results of the most effective SIR composition for the separation of Zr-Hf are comparison extractant and resin = 5:5 either for the dry method and wet method, the equilibrium equations for Zr approaching Langmuir equilibrium models while the equilibrium equation for Hf approaching Freundlich equilibrium models which the most effective adsorption results that bait comparison with the SIR = 10 mL : 5 g with β = 0.1831; η Zr = 26.39 % and η Hf = 66.19 % for dry method and β = 0.1557; η Zr = 25.17 % and η Hf = 68.36 % for wet method. From result desorption process was 2 M H_2SO_4. (author)

  16. Estimation of solubility of organo-phosphorus extractants by P determination using molybdovanadophosphoric acid method

    International Nuclear Information System (INIS)

    Gill, J.S.; Kotekar, M.K.; Singh, H.

    2005-01-01

    Solvent extraction processes have been found to be suitable for uranium recovery from phosphoric acid. Various extractants like di-2-ethyl hexylphosphoric acid (D2EHPA), di-nonylphenyl phosphoric acid (DNPPA) and synergistic agents like tri-butyl phosphate (TBP), tri-octyl phosphine oxide (TOPO) have been used in liquid-liquid extraction of uranium from phosphoric acid. Contents of these organo-phosphorus compounds in aqueous raffinates need estimation for process requirements. Solubility of Tri-butyl phosphate (TBP) and Di-2-ethylhexyl phosphoric acid (D2EHPA) extractants have been determined in different media of water, oxalic acid (0.6M) and sulphuric acid (3.75M) solutions. These compounds were estimated by determining their phosphorus (P) contents employing molybdovanadophosphoric acid method, after digesting and solubalizing them in nitric and perchloric acid. (author)

  17. Feasibility studies on supercritical fluid extraction of uranium from phosphoric acid

    International Nuclear Information System (INIS)

    Dubey, B.P.; Agarwal, A.K.

    2014-01-01

    Supercritical fluid extraction (SFE) is a promising novel technology for extraction of many materials. Work has been carried out worldwide on SFE of uranium from various matrices. However, there are no references indicating the R and D on uranium extraction from phosphoric acid using this technology. Heavy Water Board is involved in technology development for recovery of uranium from secondary source, hence it was considered prudent to investigate the technology of SFE for this purpose. Various experiments were carried out with both WPA (P 2 O 5 content 28%) and MGPA (P 2 O 5 content 54%) using bench scale facility available with one of the private party. Extraction experiments were carried out using several chelating agents including TBP, D2EHPA, D2EHPA+TBP/TOPO, TTA, TTA+TBP etc. Feasibility studies revealed the hydrodynamics of operation indicating liquid expansion by about three times during flow of super critical (SC) CO 2 . No flooding was observed when the extraction column filled 20% of its volume capacity, no carryover of entrained/extracted liquid with SC CO 2 with MGPA, material balance of inputs and outputs established i.e. 100% recovery of MGPA and chelating agent, No operational problems with raw MGPA (untreated). No significant extraction of impurities from phosphoric acid to SC CO 2 , 40℃ temperature and 160 bar pressure found ideal for extraction experiments since no other materials found extracted at these conditions and no apparent change/deterioration in PA and chelating agents. Experiments established feasibility of SCE with CO 2 , proper recovery of PA and chelating agents, no need for pretreatment/gunk removal from PA; however, extraction of uranium was found inadequate even though ORP of feed acid was boosted by H 2 O 2 addition. Investigations revealed that SCE column created reducing environment in phosphoric acid, which was not favourable for uranium extraction, which resulted in difficulty in extraction of Uranium. HWB has now designed

  18. Phosphates and phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Becker, P [Compagnie Francaise de l' Azote, Paris (France)

    1983-01-01

    In chapter 8.5 the following aspects of uranium recovery are treated: basis of extraction process, extraction principle, solvents, strength of the acid to be treated, technology, main processes in use, impact of uranium recovery on phosphoric acid plants, and economics of uranium recovery plants.

  19. Study of uranium(VI) speciation in phosphoric acid solutions and of its recovery by solvent extraction

    International Nuclear Information System (INIS)

    Dartiguelongue, Adrien

    2014-01-01

    Because small amounts of uranium are present in phosphate rocks, wet phosphoric acids may contain up to 300 ppm of uranium(VI). Therefore, such acids are a cost-effective unconventional source of this metal. Its recovery is a challenge for metallurgical firms which must develop reliable and selective solvent extraction processes. Such processes need to know the chemical equilibria involved in the extraction process, the speciation of uranium and its thermodynamics in solution. These two last points have been investigated in this work. Firstly, the most probable species of uranium(VI) in phosphoric acid solutions have been selected thanks to a detailed review of the literature. Then, a thermodynamic model founded on an equation of state for electrolytes has been built according these hypotheses. It has been validated with speciation data coming from original ATR-IR spectroscopy measurements. Finally, the composition of the aqueous phosphoric acid solutions and the activity coefficients obtained have been combined with a chemical model of uranium(VI) extraction into an organic phase containing a synergistic mixture of bis(2-ethylhexyl)phosphoric acid (D2EHPA) and tri-n-octylphosphine oxide (TOPO) in order to represent the variation of the distribution coefficient of uranium(VI) with H 3 PO 4 concentration. This model had been previously developed at Chimie ParisTech at a given concentration of H 3 PO 4 (i.e., 5,3 mol/L), but in the present study we have tested its validity in an extended range of phosphoric acid concentrations (i.e., 1-7 mol/L) and improved it. (author)

  20. Removal of Sr ions from nuclear wastes by D2EHPA+TBP based supported liquid membranes

    International Nuclear Information System (INIS)

    Chaudry, M.A.; Ahmad, I.

    2000-01-01

    Sr ions removal from nuclear wastes is of great importance. /sup 90/Sr radionuclide, due to its long half-life to disintegrate into daughter products and release of radiations, resulting from fission of uranium, produce heat and is a real problem for disposal of radioactive wastes. The separation study of Sr ions from aqueous solutions is, therefore, very important in the nuclear industry. n the present article some of the work done to develop the separation technique based on coupled transport phenomenon for Sr ions is reported. Di-2-ethyl-hexyl phosphoric acid mixed with tri-n-butyl phosphate (TBP), diluted in kerosene oil, as an organic liquid has been used as a membrane, supported in polypropylene hydrophobic films to transport Sr ions. The optimum conditions and mechanism of transport for these ions across the membrane have been described. The effect of feed complexing components i.e. tartaric acid and citric acid concentration on the flux and permeability of the Sr/sup 2+/ ions has been studied. It is shown that supported liquid membrane technique can be used as an alternate process to classical solvent extraction to remove Sr ions from nuclear industry wastes. (author)

  1. Recovery of uranium from phosphoric acid medium by polymeric composite beads encapsulating organophosphorus extractants

    Energy Technology Data Exchange (ETDEWEB)

    Singh, D.K.; Yadav, K.K.; Varshney, L.; Singh, H. [Bhabha Atomic Research Centre, Mumbai 400 085 (India)

    2013-07-01

    The present study deals with the preparation and evaluation of the poly-ethersulfone (PES) based composite beads encapsulating synergistic mixture of D2EHPA and Cyanex 923 (at 4:1 mole ratio) for the separation of uranium from phosphoric acid medium. SEM was used for the characterization of the composite materials. Addition of 1% PVA (polyvinyl alcohol) improved the internal morphology and porosity of the beads. Additionally, microscopic examination of the composite bead confirmed central coconut type cavity surrounded by porous polymer layer of the beads through which exchange of metal ions take place. Effect of various experimental variables including aqueous acidity, metal ion concentration in aqueous feed, concentration of organic extractant inside the beads, extractant to polymer ratio, liquid to solid (L/S) ratio and temperature on the extraction of uranium was studied. Increase in acidity (1-6 M), L/S ratio (1- 10), metal ion concentration (0.2-3 g/L U{sub 3}O{sub 8}) and polymer to extractant ratio (1:4 -1:10) led to decrease in extraction of uranium. At 5.5 M (comparable to wet process phosphoric acid concentration) the extraction of uranium was about 85% at L/S ratio 5. Increase in extractant concentration inside the bead resulted in enhanced extraction of metal ion. Increase in temperature in the range of 30 to 50 Celsius degrees increased the extraction, whereas further increase to 70 C degrees led to the decrease in extraction of uranium. Amongst various reagents tested, stripping of uranium was quantitative by 12% Na{sub 2}CO{sub 3} solution. Polymeric beads were found to be stable and reusable up-to 10 cycles of extraction/stripping. (authors)

  2. Recovering uranium from phosphoric acid

    International Nuclear Information System (INIS)

    Anon.

    1979-01-01

    Wet-process phosphoric acid contains a significant amount of uranium. This uranium totals more than 1,500 tons/yr in current U.S. acid output--and projections put the uranium level at 8,000 tons/yr in the year 2000. Since the phosphoric acid is a major raw material for fertilizers, uranium finds its way into those products and is effectively lost as a resource, while adding to the amount of radioactive material that can contaminate the food chain. So, resource-conservation and environmental considerations both make recovery of the uranium from phosphoric acid desirable. This paper describes the newly developed process for recovering uranium from phosphoric acid by using solvent-extraction technique. After many extractants had been tested, the researchers eventually selected the combination of di (2-ethylhexyl) phosphoric acid (DEPA) and trioctylphosphine oxide (TOPO) as the most suitable. The flowscheme of the process is included

  3. Uranium extraction from phosphoric acid

    International Nuclear Information System (INIS)

    Araujo Figueiredo, C. de

    1984-01-01

    The recovery of uranium from phosphoric liquor by two extraction process is studied. First, uranium is reduced to tetravalent condition and is extracted by dioctypyrophosphoric acid. The re-extraction is made by concentrated phosphoric acid with an oxidizing agent. The re-extract is submitted to the second process and uranium is extracted by di-ethylhexilphosphoric acid and trioctylphosphine oxide. (M.A.C.) [pt

  4. Uranium extraction from phosphoric acid

    International Nuclear Information System (INIS)

    Lounis, A.

    1983-05-01

    A study has been carried out for the extraction of uranium from phosphoric acid produced in Algeria. First of all, the Algerian phosphoric acid produced in Algeria by SONATRACH has been characterised. This study helped us to synthesize a phosphoric acid that enabled us to pass from laboratory tests to pilot scale tests. We have then examined extraction and stripping parameters: diluent, DZEPHA/TOPO ratio and oxidising agent. The laboratory experiments enabled us to set the optimum condition for the choice of diluent, extractant concentration, ratio of the synergic mixture, oxidant concentration, redox potential. The equilibrium isotherms lead to the determination of the number of theoretical stages for the uranium extraction and stripping of uranium, then the extraction from phosphoric acid has been verified on a pilot scale (using a mixer-settler)

  5. Stripping of Uranium (IV) from D2EHPA + TBP system with ammonium oxalate and its recovery as uranium peroxide

    International Nuclear Information System (INIS)

    Singh, D.K.; Singh, H.

    2014-01-01

    Uranium is an important fissile material for the generation of electricity by nuclear reactors. To obtain uranium as a final product meeting the stringent nuclear specifications, many process steps are involved starting from ore processing to the precipitation of yellow cake. Solvent extraction is one of the process industrially adopted worldwide to achieve such purity of uranium from leach liquor and usually uses amine or organophosphorus types of extractant depending upon the composition of feed material. In solvent extraction technique, stripping is a prominent hydrometallurgical operation which brings the metal values of interest in aqueous solution for further treatment. In the case of uranium, stripping is dependent on its oxidation state. For hexavalent state generally carbonate solutions are used, where as in the case of tetravalent form salt solution such as ammonium oxalate is effective. Use of ammonium oxalate as stripping agent for tetravalent uranium from pyrophosphoric acid has been reported in patent however the details are not disclosed. In the present investigation an effort has been made to investigate the stripping behaviour of uranium from a synthetically loaded synergistic solvent mixture of uranium in tetravalent state

  6. Recovering uranium from phosphoric acid

    International Nuclear Information System (INIS)

    Abodishish, H.A.; Ritchey, R.W.

    1982-01-01

    Precipitation of Fe 3 HN 4 H 8 (PO 4 ) 6 is prevented in the second cycle extractor, in a two cycle uranium recovery process, by washing ammonia laden organic solvent stream, from the second cycle stripper, with first cycle raffinate iron stream containing phosphoric acid, prior to passing the solvent stream into the second cycle extractor. (author)

  7. 21 CFR 182.1073 - Phosphoric acid.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Phosphoric acid. 182.1073 Section 182.1073 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) FOOD FOR HUMAN....1073 Phosphoric acid. (a) Product. Phosphoric acid. (b) Conditions of use. This substance is generally...

  8. 21 CFR 582.1073 - Phosphoric acid.

    Science.gov (United States)

    2010-04-01

    ... 21 Food and Drugs 6 2010-04-01 2010-04-01 false Phosphoric acid. 582.1073 Section 582.1073 Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) ANIMAL... Additives § 582.1073 Phosphoric acid. (a) Product. Phosphoric acid. (b) Conditions of use. This substance is...

  9. Uranium extraction in phosphoric acid

    International Nuclear Information System (INIS)

    Araujo Figueiredo, C. de

    1984-01-01

    Uranium is recovered from the phosphoric liquor produced from the concentrate obtained from phosphorus-uraniferous mineral from Itataia mines (CE, Brazil). The proposed process consists of two extraction cycles. In the first one, uranium is reduced to its tetravalent state and then extracted by dioctylpyrophosphoric acid, diluted in Kerosene. Re-extraction is carried out with concentrated phosphoric acid containing an oxidising agent to convert uranium to its hexavalent state. This extract (from the first cycle) is submitted to the second cycle where uranium is extracted with DEPA-TOPO (di-2-hexylphosphoric acid/tri-n-octyl phosphine oxide) in Kerosene. The extract is then washed and uranium is backextracted and precipitated as commercial concentrate. The organic phase is recovered. Results from discontinuous tests were satisfactory, enabling to establish operational conditions for the performance of a continuous test in a micro-pilot plant. (Author) [pt

  10. Application of strong phosphoric acid to radiochemistry

    International Nuclear Information System (INIS)

    Terada, Kikuo

    1977-01-01

    Not only inorganic and organic compounds but also natural substrances, such as accumulations in soil, are completely decomposed and distilled by heating with strong phosphoric acid for 30 to 50 minutes. As applications of strong phosphoric acid to radiochemistry, determination of uranium and boron by use of solubilization effect of this substance, titration of uranyl ion by use of sulfuric iron (II) contained in this substance, application to tracer experiment, and determination of radioactive ruthenium in environmental samples are reviewed. Strong phosphoric acid is also applied to activation analysis, for example, determination of N in pyrographite with iodate potassium-strong phosphoric acid method, separation of Os and Ru with sulfuric cerium (IV) - strong phosphoric acid method or potassium dechromate-strong phosphoric acid method, analysis of Se, As and Sb rocks and accumulations with ammonium bromide, sodium chloride and sodium bromide-strong phosphoric acid method. (Kanao, N.)

  11. Consumption of Pt anode in phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Kamiya, N.; Urata, K.; Motohira, N.; Ota, K. [Yokohama National University, Yokohama (Japan)

    1997-12-05

    Consumption of Pt anode was investigated in phosphoric acid of various concentration. In 30-70wt% phosphoric acid, Pt dissolved at the rate of 19{mu}gcm{sup -2}h{sup -1}. On the other hand, in 85 wt% phosphoric acid, the amount increased to 0.91 mgcm{sup -2}h{sup -1} which is ca. 180 and 1800 times as much as in 1M sulfuric acid and 1M alkaline solution, respectively. In the diluted phosphoric acid solution, the Pt surface was covered with Pt oxides during the electrolysis, which would prevent the surface from corrosion. However, in the concentrated phosphoric acid, no such oxide surface was observed. Concentrated phosphoric acid might form stable complex with Pt species, therefore the uncovered bare Pt surface is situated in the serious corrosion condition under the high overvoltage and Pt would dissolve into the solution directly instead of forming the Pt oxides. 11 refs., 9 figs., 1 tab.

  12. Pretreatment of industrial phosphoric acid by Algerian filter-aids

    International Nuclear Information System (INIS)

    Mellah, A.; Setti, Louisa; Chegrouche, Salah

    1993-01-01

    The present work involves the filtration of industrial phosphoric acid by different filter-aids such as kieselguhr, celite and bleaching clay. The retention of substances contained in wet phosphoric acid was determined using the three filter-aids. Thus, the phosphoric acid, obtained by filtration on kieselguhr has the same specifications as technical phosphoric acid produced by Rhone-Poulenc (France) as standard

  13. Method of purifying phosphoric acid after solvent extraction

    International Nuclear Information System (INIS)

    Kouloheris, A.P.; Lefever, J.A.

    1979-01-01

    A method of purifying phosphoric acid after solvent extraction is described. The phosphoric acid is contacted with a sorbent which sorbs or takes up the residual amount of organic carrier and the phosphoric acid separated from the organic carrier-laden sorbent. The method is especially suitable for removing residual organic carrier from phosphoric acid after solvent extraction uranium recovery. (author)

  14. 46 CFR 151.50-23 - Phosphoric acid.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Phosphoric acid. 151.50-23 Section 151.50-23 Shipping... BULK LIQUID HAZARDOUS MATERIAL CARGOES Special Requirements § 151.50-23 Phosphoric acid. (a) The term phosphoric acid as used in this subpart shall include, in addition to phosphoric acid, aqueous solutions of...

  15. Electrolyte Additives for Phosphoric Acid Fuel Cells

    DEFF Research Database (Denmark)

    Gang, Xiao; Hjuler, H.A.; Olsen, C.A.

    1993-01-01

    , as a fuel-cell performance with the modified electrolytes. Specific conductivity measurements of some of the modified phosphoric acid electrolytes are reported. At a given temperature, the conductivity of the C4F9SO3K-modified electrolyte decreases with an increasing amount of the additive; the conductivity...... of the remains at the same value as the conductivity of the pure phosphoric acid. At a given composition, the conductivity of any modified electrolyte increases with temperature. We conclude that the improved cell performance for modified electrolytes is not due to any increase in conductivity.......Electrochemical characteristics of a series of modified phosphoric acid electrolytes containing fluorinated car on compounds and silicone fluids as additives are presented. When used in phosphoric acid fuel cells, the modified electrolytes improve the performance due to the enhanced oxygen...

  16. Counter current extraction of phosphoric acid: Food grade acid production

    International Nuclear Information System (INIS)

    Shlewit, H.; AlIbrahim, M.

    2009-01-01

    Extraction, scrubbing and stripping of phosphoric acid from the Syrian wet-phosphoric acid was carried out using Micro-pilot plant of mixer settler type of 8 l/h capacity. Tributyl phosphate (TBP)/di-isopropyl ether (DIPE) in kerosene was used as extractant. Extraction and stripping equilibrium curves were evaluated. The number of extraction and stripping stages to achieve the convenient and feasible yield was determined. Detailed flow sheet was suggested for the proposed continuous process. Data obtained include useful information for the design of phosphoric acid extraction plant. The produced phosphoric acid was characterized using different analytical techniques. (author)

  17. Pretreatment of phosphoric acid for uranium recovery by the wet phosphoric acid process

    International Nuclear Information System (INIS)

    Chern, S.L.P.; Chen, Y.C.L.; Chang, S.S.H.; Kuo, T.S.; Ting, G.C.M.

    1980-01-01

    The proposal deals with reprocessing of phosphoric acid arising from uranium separation according to the wet phosphoric acid process and being intended for recycling. In detail, the sludge will be removed by means of an inclined separating device containing corrugated plates, then the organic impurities are washed out with kerosene in suitable facilities, and the crude phase remaining in the settling tank will be separated from the kerosene in a separating centrifuge. The method has only got low cost of installation. (UWI) [de

  18. Process for recovering a uranium containing concentrate and purified phosphoric acid from a wet process phosphoric acid containing uranium

    International Nuclear Information System (INIS)

    Weterings, C.A.M.; Janssen, J.A.

    1985-01-01

    A process is claimed for recovering from a wet process phosphoric acid which contains uranium, a uranium containing concentrate and a purified phosphoric acid. The wet process phosphoric acid is treated with a precipitant in the presence of a reducing agent and an aliphatic ketone

  19. Process for recovering a uranium containing concentrate and purified phosphoric acid from a wet process phosphoric acid containing uranium

    Energy Technology Data Exchange (ETDEWEB)

    Weterings, C.A.M.; Janssen, J.A.

    1985-04-30

    A process is claimed for recovering from a wet process phosphoric acid which contains uranium, a uranium containing concentrate and a purified phosphoric acid. The wet process phosphoric acid is treated with a precipitant in the presence of a reducing agent and an aliphatic ketone.

  20. Uranium recovery from wet process phosphoric acid

    International Nuclear Information System (INIS)

    1980-01-01

    In the field of metallurgy, specifically processes for recovering uranium from wet process phosphoric acid solution derived from the acidulation of uraniferous phosphate ores, problems of imbalance of ion exchange agents, contamination of recycled phosphoric acid with process organics and oxidizing agents, and loss and contamination of uranium product, are solved by removing organics from the raffinate after ion exchange conversion of uranium to uranous form and recovery thereof by ion exchange, and returning organics to the circuit to balance mono and disubstituted ester ion exchange agents; then oxidatively stripping uranium from the agent using hydrogen peroxide; then after ion exchange recovery of uranyl and scrubbing, stripping with sodium carbonate and acidifying the strip solution and using some of it for the scrubbing; regenerating the sodium loaded agent and recycling it to the uranous recovery step. Economic recovery of uranium as a by-product of phosphate fertilizer production is effected. (author)

  1. Uranium recovery from wet-process phosphoric acid

    International Nuclear Information System (INIS)

    McCullough, J.F.; Phillips, J.F. Jr.; Tate, L.R.

    1979-01-01

    A method of recovering uranium from wet-process phosphoric acid is claimed where the acid is treated with a mixture of an ammonium salt or ammonia, a reducing agent, and then a miscible solvent. Solids are separated from the phosphoric acid liquid phase. The solid consists of a mixture of metal phosphates and uranium. It is washed free of adhering phosphoric acid with fresh miscible solvent. The solid is dried and dissolved in acid whereupon uranium is recovered from the solution. Miscible solvent and water are distilled away from the phosphoric acid. The distillate is rectified and water discarded. All miscible solvent is recovered for recycle. 5 claims

  2. Uranium recovery from wet process phosphoric acid

    International Nuclear Information System (INIS)

    Carrington, O.F.; Pyrih, R.Z.; Rickard, R.S.

    1981-01-01

    Improvement in the process for recovering uranium from wetprocess phosphoric acid solution derived from the acidulation of uraniferous phosphate ores by the use of two ion exchange liquidliquid solvent extraction circuits in which in the first circuit (A) the uranium is reduced to the uranous form; (B) the uranous uranium is recovered by liquid-liquid solvent extraction using a mixture of mono- and di-(Alkyl-phenyl) esters of orthophosphoric acid as the ion exchange agent; and (C) the uranium oxidatively stripped from the agent with phosphoric acid containing an oxidizing agent to convert uranous to uranyl ions, and in the second circuit (D) recovering the uranyl uranium from the strip solution by liquid-liquid solvent extraction using di(2ethylhexyl)phosphoric acid in the presence of trioctylphosphine oxide as a synergist; (E) scrubbing the uranium loaded agent with water; (F) stripping the loaded agent with ammonium carbonate, and (G) calcining the formed ammonium uranyl carbonate to uranium oxide, the improvement comprising: (1) removing the organics from the raffinate of step (B) before recycling the raffinate to the wet-process plant, and returning the recovered organics to the circuit to substantially maintain the required balance between the mono and disubstituted esters; (2) using hydogren peroxide as the oxidizing agent in step (C); (3) using an alkali metal carbonate as the stripping agent in step (F) following by acidification of the strip solution with sulfuric acid; (4) using some of the acidified strip solution as the scrubbing agent in step (E) to remove phosphorus and other impurities; and (5) regenerating the alkali metal loaded agent from step (F) before recycling it to the second circuit

  3. Method of recovering phosphoric acid type decontaminating electrolytes by electrodeposition

    International Nuclear Information System (INIS)

    Sasaki, Takashi; Wada, Koichi; Kobayashi, Toshio.

    1985-01-01

    Purpose: To recoving phosphoric acid type highly concentrated decontaminating liquid used for the electrolytic decontamination of contaminated equipments, components, etc in nuclear power plants or the like through electrodeposition by diaphragm electrolysis. Method: Before supplying phosphoric acid decontaminating liquid at high concentration used in the electrolytic decontaminating step to an electrodeposition recovering tank, phosphoric acid in the decontaminating electrolyte is extracted with solvents and decomposed liquid extracts (electrolyte reduced with the phosphoric acid component) are supplied to the cathode chamber of the electrodeposition recovering tank, where phosphoric acid is back-extracted with water from the solvents after extraction of phosphoric acid. Then, the back-extracted liquids (aqueous phosphoric acid solution scarcely containing metal ions) are sent to the anode chamber of the electrodeposition recovering tank. Metal ions in the liquid are captured by electrodeposition in the cathode chamber, as well as phosphoric acid in the liquids is concentrated to the initial concentration of the electrolyte in the anode chamber for reuse as the decontaminating electrolyte. As the phosphoric acid extracting agent used in the electrodeposition recovering step for the decontaminating electrolyte, water-insoluble and non-combustible tributyl phosphate (TBP) is most effective. (Horiuchi, T.)

  4. Separation of rare earths from solutions of phosphoric acid

    International Nuclear Information System (INIS)

    Jones, E.A.

    1977-01-01

    Rare earths are separated from 6M phosphoric acid by adsorption onto cation resin BIORAD AG50W-X8. The phosphoric acid is then washed from the column, and the rare earths are eluted with 4M hydrochloric acid

  5. Pretreatment of phosphoric acid of Annaba

    International Nuclear Information System (INIS)

    Kada, R.

    1990-03-01

    The most important step in the process of uranium recovery from phosphoric acid is the pretreatment operation. In this study, the adsorption of organic matters on activated carbon was carried out in a batch process and in a fixed bed column. First, the chemical and physical characterization of phosphoric acid, activated carbon and gypsum were performed. In addition, the organic matters were qualitatively analysed and a new and original quantitative method was experimented. Next, the various operating parameters such as agitation speed, granulometry, temperature, solid/liquid ratio, initial concentration, acid flowrate, and bed height were optimized. The experimental equilibrium isotherm was compared to the Langmuir, Freundlich, and Redlich-Peterson theoretical isotherms. It was noticed that the three models did not fit the experimental isotherm in the total concentration range. Thus, an original bilinear model was proposed. The influence of the operating conditions on the adsorption kinetics was also investigated. As a result of that, a new mathematical model was proposed to determine both the liquid and solid phases mass transfer and the solid phase diffusion coefficient. Finally, adsorption of organic matters on a fixed bed process allowed computation of the number of transfer units (NTU), the height of adsorption zone and the degree of saturation of activated carbon

  6. Influence of modifiers on the separation of dysprosium from neodymium using organophosphorus acid derivates

    Energy Technology Data Exchange (ETDEWEB)

    Elwert, Tobias; Schwarz, Sabrina; Goldmann, Daniel [TU Clausthal, Clausthal-Zellerfeld (Germany). Lehrstuhl fuer Rohstoffaufbereitung und Recycling

    2016-01-15

    The aim of this study was to investigate the applicability of three organophosphorus acid derivates (D2EHPA, EHEHPA and Cyanex 572) for the separation of terbium and dysprosium from praseodymium and neodymium from NdFeB magnets in chloride solution. A special focus was put on the effect of phase modifiers. The investigations revealed that all extractants show in general a similar extraction behavior but the extraction is shifted to higher pH values in the order D2EHPA < EHEHPA < Cyanex 572. Therefore, and due to higher realizable loadings, EHEHPA and Cyanex 572 are more suitable for the investigated separation problem than D2EHPA. Whereas EHEHPA requires 1-decanol as phase modifier, Cyanex 572 can be employed without modifier addition.

  7. Acid distribution in phosphoric acid fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Okae, I.; Seya, A.; Umemoto, M. [Fuji Electric Co., Ltd., Chiba (Japan)

    1996-12-31

    Electrolyte acid distribution among each component of a cell is determined by capillary force when the cell is not in operation, but the distribution under the current load conditions had not been clear so far. Since the loss of electrolyte acid during operation is inevitable, it is necessary to store enough amount of acid in every cell. But it must be under the level of which the acid disturbs the diffusion of reactive gases. Accordingly to know the actual acid distribution during operation in a cell is very important. In this report, we carried out experiments to clarify the distribution using small single cells.

  8. World wide IFC phosphoric acid fuel cell implementation

    Energy Technology Data Exchange (ETDEWEB)

    King, J.M. Jr

    1996-04-01

    International Fuel Cells, a subsidary of United technologies Corporation, is engaged in research and development of all types of fuel cell technologies and currently manufactures alkaline fuel cell power plants for the U.S. manned space flight program and natural gas fueled stationary power plants using phosphoric acid fuel cells. This paper describes the phosphoric acid fuel cell power plants.

  9. Phosphor investigation in the production of Syrian phosphoric acid using Nuclear Magnetic Resonance

    International Nuclear Information System (INIS)

    Al-Hassanieh, O.; Al-Hameish, M.

    2009-06-01

    Nuclear magnetic resonance spectroscopy (NMR) was applied in this work to the industrial process of extraction of uranium from phosphoric acid and to the process of the purification of the phosphoric acid for food proposes. The structural changes of used extraction materials and the organic content of the final product was studied. 13 C , 1 H and 32 P-spectra of all material during the process were recorded. The spectra of the three used extraction materials Bis(2-ethylhexyl Phosphoric Acid)) DEHPA, TriOctyl Phosphine Oxide (TOPO) (C 8 H 1 7) 3 P=O and TriButyl Phosphate (TBP) (C 4 H 9 O) 3 P=O show a partial degradation during the process. The final product ( Phosphoric acid for Food proposes) doesn't contain any organic solvents or extraction material. (author)

  10. Process for winning uranium from wet process phosphoric acid

    International Nuclear Information System (INIS)

    1980-01-01

    A process is described for winning uranium from wet process phosphoric acid by means of liquid-liquid extraction with organic phosphoric acid esters. The process is optimised by keeping the sulphate percentage in the phosphoric acid below 2% by weight, and preferably below 0.6% by weight, as compared to P 2 O 5 in the phosphoric acid. This is achieved by adding an excess of Ba and/or Ca carbonate or sulfide solution and filtering off the formed calcium and/or barium sulphate precipitates. Solid KClO 3 is then added to the filtrate to oxidise U 4+ to U 6+ . The normal extraction procedure using organic phosphoric esters as extraction liquid, can then be applied. (Th.P.)

  11. The preparation of 32P labelled phosphorous acid

    International Nuclear Information System (INIS)

    Henderson, D.; Jenkinson, A.; Sorby, P.

    1986-11-01

    Phosphorous acid labelled with 32 P has been prepared, on a small scale, starting from neutron-irradiated phosphorus. The compound is intended for tracer studies in the development of novel fungicides

  12. Phosphoric acid fuel cell platinum use study

    Science.gov (United States)

    Lundblad, H. L.

    1983-05-01

    The U.S. Department of Energy is promoting the private development of phosphoric acid fuel cell (PAFC) power plants for terrestrial applications. Current PAFC technology utilizes platinum as catalysts in the power electrodes. The possible repercussions that the platinum demand of PAFC power plant commercialization will have on the worldwide supply and price of platinum from the outset of commercialization to the year 2000 are investigated. The platinum demand of PAFC commercialization is estimated by developing forecasts of platinum use per unit of generating capacity and penetration of PAFC power plants into the electric generation market. The ability of the platinum supply market to meet future demands is gauged by assessing the size of platinum reserves and the capability of platinum producers to extract, refine and market sufficient quantities of these reserves. The size and timing of platinum price shifts induced by the added demand of PAFC commercialization are investigated by several analytical methods. Estimates of these price shifts are then used to calculate the subsequent effects on PAFC power plant capital costs.

  13. Preparation of high purification and food grade phosphoric acid from technical grade phosphoric acid by liquid-liquid detraction method

    International Nuclear Information System (INIS)

    Alimoradi, M.; Borji, F.; Kishani, A.

    2002-01-01

    Pay attention to increasing consumption of high purification and food grade phosphoric acid in various industries and food industries and on in on hand and lack of preparation between production and distribution of this products its purification is so vital. In this article of liquid-liquid extraction method with normal hexane-mixture of ammonia and acetone-diisopropyl alcohol and normal butanol solvents and these determination of distribution coefficient each one with ph-me try titration we can evaluate effectiveness and sufficiency each one. Because of proper coefficient distribution and its local production of normal butanol solvent and low price is the best solvent. To phosphoric acid modifying coefficient distribution for extraction of phosphoric acid we can add a little value sulfuric acid to the mixture and to remove flouride impurity we add a little Na 2 O. After extraction stage extracted phosphoric acid in the normal strips by evaluating with distilled water and then by passing the carbon active bed and following passes of cationic resine column and concentrated with vacuum distillation. Conclusion of this article is produce of phosphoric acid 85% w/w and food grade from impure phosphoric acid 52% w/w with technical grade

  14. Process for recovery of uranium from wet process phosphoric acid

    International Nuclear Information System (INIS)

    Wiewiorowski, T.K.; Thornsberry, W.L. Jr.

    1978-01-01

    Process is claimed for the recovery of uranium from wet process phosphoric acid solution in which an organic extractant, containing uranium values and dissolved iron impurities and comprising a dialkylphosphoric acid and a trialkylphosphine oxide dissolved in a water immiscible organic solvent, is contacted with a substantially iron-free dilute aqueous phosphoric acid to remove said iron impurities. The removed impurities are bled from the system by feeding the resulting iron-loaded phosphoric acid to a secondary countercurrent uranium extraction operation from which they leave as part of the uranium-depleted acid raffinate. Also, process for recovering uranium in which the extractant, after it has been stripped of uranium values by aqueous ammonium carbonate, is contacted with a dilute aqueous acid selected from the group consisting of H 2 SO 4 , HCl, HNO 3 and iron-free H 3 PO 4 to improve the extraction efficiency of the organic extractant

  15. Transport of phosphoric acid through supported liquid membrane

    International Nuclear Information System (INIS)

    Zayzafoon, G.; Yassine, T.; Baidoun, R.

    2003-01-01

    The transport of phosphhoric acid through liquid membranes of amylalkohol, 1-octanol and 2-octanol was studied. It was found that phosphoric acid is transfered from feed side to strip side and the transport increased with the concentration of phosphoric acid up to 5M. The permeability in each membrane was determined for 5M phosphoic acid. It was found that the permeability values are 1.45 x 10 1 0 m 2 s 1 for amylakohol and ∼ 1x10 1 0 m 2 s 1 for each of 1-octanol and 2-octanol

  16. Cadmium elemination from phosphoric acid by ionic flotation

    International Nuclear Information System (INIS)

    Brikci-Nigassa, Mounir; Hamouche, Hafida

    1995-11-01

    The ion flotation process for the recovery of cadmium from wet phosphoric acid (30%P2O5) has been studied. This technique combines a chemical recation between the collector and the cadmium to form a precipitate (sublate) which is carried to the surface of the solution by air bubbles. the resulting foam containing the cadmium may then separated from solution. The influence of parameters such as collector and cadmium concentration as well as iron content have been investigated for the case a synthetic acid (30% P2O5). The result have been applied to the industrial phosphoric acid produced from Djebel Onk's phosphates (Algeria)

  17. Reactivity of the cadmium ion in concentrated phosphoric acid solutions.

    Science.gov (United States)

    De Gyves, J; Gonzales, J; Louis, C; Bessiere, J

    1989-07-01

    The solvation transfer coefficients which characterize the changes of ion reactivity with phosphoric acid concentration have been calculated for cadmium from the constants of the successive chloride complexes, and for silver and diethyldithiophosphate from potentiometric measurements. They evidence the strong desolvation of the cadmium species in concentrated phosphoric acid media, causing a remarkable increase of its reactivity. They allow the results of liquid-liquid extraction, precipitation and flotation reactions to be correctly interpreted and their changes to be foreseen when the reagents are modified.

  18. Phosphoric acid fuel cell R and D activities at KACST

    International Nuclear Information System (INIS)

    Ghouse, M.; Aba-Oud, H.; Ba-Junaid, M.; Al-Garni, M.; Quadri, M.I.

    1993-01-01

    The PAFC (Phosphoric Acid Fuel Cell) activities are directed towards the development of components of single cell and experimental stacks at KACST. The main aim of the present task is to design and construct a 1 kW PAFC Stack and demonstrate it by integrating with an electrolyser using a DC current generated by a photovoltaic power source. This paper describes the preparation of porous teflon bonded gas diffusion carbon electrodes and their evaluation as single phosphoric acid fuel cells using hydrogen as a fuel and oxygen/air as an oxidant. 6 figs., 2 tabs., 15 refs

  19. Properties of precipitates formed during ammonization of extractional phosphoric acid

    International Nuclear Information System (INIS)

    Zakharova, B.S.; Komissarova, L.N.; Naumov, S.V.; Traskin, V.Yu.

    1992-01-01

    Dimensions of precipitated rare-earth phosphate particles -(0.1 μm)- are near the boundary of colloidal system sedimentation stability range at neutralization of extraction phosphoric acid. Thus, formation of multiple aggregates of colloidal particles results in immediate sedimentation of the precipitate. Processes occurring within the system may be described using second order reaction equation. Average efficient size of precipitates grows at reduction of reaction mixture pH. About 30% of rare-earth elements and yttrium in the extraction phosphoric acid is extracted from it; concentration of rare-earth elements, yttrium and scandium in precipitate is maximum 2 mass. %

  20. Solid-state actinide acid phosphites from phosphorous acid melts

    International Nuclear Information System (INIS)

    Oh, George N.; Burns, Peter C.

    2014-01-01

    The reaction of UO 3 and H 3 PO 3 at 100 °C and subsequent reaction with dimethylformamide (DMF) produces crystals of the compound (NH 2 (CH 3 ) 2 )[UO 2 (HPO 2 OH)(HPO 3 )]. This compound crystallizes in space group P2 1 /n and consists of layers of uranyl pentagonal bipyramids that share equatorial vertices with phosphite units, separated by dimethylammonium. In contrast, the reaction of phosphorous acid and actinide oxides at 210 °C produces a viscous syrup. Subsequent dilution in solvents and use of standard solution-state methods results in the crystallization of two polymorphs of the actinide acid phosphites An(HPO 2 OH) 4 (An=U, Th) and of the mixed acid phosphite–phosphite U(HPO 3 )(HPO 2 OH) 2 (H 2 O)·2(H 2 O). α- and β-An(HPO 2 OH) 4 crystallize in space groups C2/c and P2 1 /n, respectively, and comprise a three-dimensional network of An 4+ cations in square antiprismatic coordination corner-sharing with protonated phosphite units, whereas U(HPO 3 )(HPO 2 OH) 2 (H 2 O) 2 ·(H 2 O) crystallizes in a layered structure in space group Pbca that is composed of An 4+ cations in square antiprismatic coordination corner-sharing with protonated phosphites and water ligands. We discuss our findings in using solid inorganic reagents to produce a solution-workable precursor from which solid-state compounds can be crystallized. - Graphical abstract: Reaction of UO 3 and H 3 PO 3 at 100 °C and subsequent reaction with DMF produces crystals of (NH 2 (CH 3 ) 2 )[UO 2 (HPO 2 OH)(HPO 3 )] with a layered structure. Reaction of phosphorous acid and actinide oxides at 210 °C produces a viscous syrup and further solution-state reactions result in the crystallization of the actinide acid phosphites An(HPO 2 OH) 4 (An=U, Th), with a three-dimensional network structure, and the mixed acid phosphite–phosphite U(HPO 3 )(HPO 2 OH) 2 (H 2 O) 2 ·(H 2 O) with a layered structure. - Highlights: • U(VI), U(IV) and Th(IV) phosphites were synthesized by solution

  1. Purification of di-nonyl phenyl phosphoric acid (DNPPA) for synergistic extraction of uranium from strong phosphoric acid

    International Nuclear Information System (INIS)

    Singh, D.K.; Vijayalakshmi, R.; Singh, H.; Sharma, J.N.; Ruhela, R.

    2009-01-01

    Di-nonyl phenyl phosphoric acid (DNPPA) obtained from various synthesis methods is always associated with impurities such as mono-nonyl phenyl phosphoric acid and nonyl phenol which need to be separated for its effective use in the extraction of uranium from strong phosphoric acid. Two methods of purification namely liquid-solid separation method using neodymium salt and liquid-liquid separation method using methylene glycol have been described. In the liquid solid separation method the purity of DNPPA obtained was about 95% with less than 1.0% monoester, however it heavily suffers in the recovery aspect which is of the order of 50-60%. The methylene glycol treatment method, results in high purity and recovery of the product. Purity obtained was about 95.0% diester and less than 0.5% monoester and recovery was more than 90%. Analysis of DNPPA was done by potentiometric titration method using autotitrator. (author)

  2. Method for the recovery of uranium from a concentrate using pure phosphoric acid

    International Nuclear Information System (INIS)

    1980-01-01

    Procedure for the recovery of an uranium bearing concentrate and pure phosphoric acid from a wet process phosphoric acid from the treatment fluid with a precipitation means in conjunction with an organic diluent, the thus formed precipitate to separate and from the remaining mixture of phosphoric acid and diluent the phosphoric acid to extract, characterised in that one applies an inorganic fluorine compound. (G.C.)

  3. Phosphors

    International Nuclear Information System (INIS)

    1975-01-01

    This invention relates to phosphors that can be used in fluorescent lamps and display devices. The phosphor is comprised of a halophosphate of calcium and/or strontium of apatite crystal structure activated with trivalent cerium and trivalent terbium. The phosphor can further include manganese. Preferably, the phosphor includes up to 10% by weight of one or more of the alkali metals lithium, sodium and potassium in the form of a compound or compounds thereof. The emissions appear as a number of fairly narrow discrete bands. The temperature of preparation is 1000degC (as opposed to the usual 1450degC), therefore reducing costs (less energy is needed, more crucibles are readily obtainable and there is no need for special conditions to enable crucibles to overcome thermal shock)

  4. 46 CFR 153.558 - Special requirements for phosphoric acid.

    Science.gov (United States)

    2010-10-01

    ... CARGOES SHIPS CARRYING BULK LIQUID, LIQUEFIED GAS, OR COMPRESSED GAS HAZARDOUS MATERIALS Design and... containment system must be: (a) Lined with natural rubber or neoprene; (b) Lined with a material approved for phosphoric acid tanks by the Commandant (CG-522); or (c) Made of a stainless steel that resists corrosion by...

  5. Fluoride removal performance of phosphoric acid treated lime ...

    African Journals Online (AJOL)

    Fluoride in drinking water above permissible levels is responsible for dental and skeletal fluorosis. In this study, removal of fluoride ions from water using phosphoric acid treated lime was investigated in continuous and point-of-use system operations. In the continuous column operations, fluoride removal performance was ...

  6. Corrosion of graphite composites in phosphoric acid fuel cells

    Science.gov (United States)

    Christner, L. G.; Dhar, H. P.; Farooque, M.; Kush, A. K.

    1986-01-01

    Polymers, polymer-graphite composites and different carbon materials are being considered for many of the fuel cell stack components. Exposure to concentrated phosphoric acid in the fuel cell environment and to high anodic potential results in corrosion. Relative corrosion rates of these materials, failure modes, plausible mechanisms of corrosion and methods for improvement of these materials are investigated.

  7. Natural Radiation in byproducts of the production of phosphoric acid

    International Nuclear Information System (INIS)

    Silveira, Marcilei A. Guazzelli da; Cardoso, L.L.; Medina, N.H.

    2014-01-01

    Natural radiation is the largest source of radiation exposure to which man is subject. It is formed basically by cosmic radiation and the radionuclides present in the Earth crust, as 40 K and the elements of the decay series of 232 Th and 238 U. Phosphate ores, which constitutes the raw material for the production of phosphoric acid, have a high rate of natural radiation from the decay series of 232 Th and 238 U. Phosphogypsum, which is naturally radioactivity, is a by-product of the production of phosphoric acid by the wet method. For each ton of phosphoric acid it is produced about 4.5 tons of phosphogypsum. This work presents the analysis of samples collected in all stages of the manufacturing process of phosphoric acid, which generates the phosphogypsum. Gamma-ray spectrometry was used to measure the concentration of the elements of the decay series of 232 Th and 238 U. All analyzed samples showed a high concentration of radionuclides, promoting the need for further steps in the process in order to reduce the presence of such radionuclides in the phosphogypsum. The results indicate the radionuclide 238 U has higher contribution in some samples of the intermediate stages of the process. All samples exceeded the international average range of human exposure to terrestrial gamma radiation, which is 0.3 to 1.0 mSv/year. (author)

  8. Process for recovering yttrium and lanthanides from wet-process phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Janssen, J.A.; Weterings, C.A.

    1983-06-28

    Process for recovering yttrium and lanthanides from wet-process phosphoric acid by adding a flocculant to the phosphoric acid, separating out the resultant precipitate and then recovering yttrium and lanthanides from the precipitate. Uranium is recovered from the remaining phosphoric acid.

  9. Synthesis of novel acid electrolytes for phosphoric acid fuel cells

    Science.gov (United States)

    Adcock, James L.

    1988-11-01

    A 40 millimole per hour scale aerosol direct fluorination reactor was constructed. F-Methyl F-4-methoxybutanoate and F-4-methoxybutanoyl fluoride were synthesized by aerosol direct fluorination of methyl 4-methoxybutanoate. Basic hydrolysis of the perfluorinated derivatives produce sodium F-4 methoxybutanoate which was pyrolyzed to F-3-methoxy-1-propene. Purification and shipment of 33 grams of F-3-methoxy-1-propene followed. Syntheses by analogous methods allowed production and shipment of 5 grams of F-3-ethoxy 1-propene, 18 grams of F-3-(2-methoxy.ethoxy) 1-propene, and 37 grams of F-3,3-dimethyl 1-butene. Eighteen grams of F-2,2-dimethyl 1-chloropropane was produced directly and shipped. As suggested by other contractors, 5 grams of F-3-methoxy 1-iodopropane, and 5 grams of F-3-(2-methoxy.ethoxy) 1-iodopropane were produced by converting the respective precursor acid sodium salts produced for olefin synthesis to the silver salts and pyrolyzing them with iodine. Each of these compounds was prepared for the first time by the aerosol fluorination process during the course of the contract. These samples were provided to other Gas Research Institute (GRI) contractors for synthesis of perfluorinated sulfur (VI) and phosphorous (V) acids.

  10. Determination of vanadium in Syrian commercial and raffinate phosphoric acid

    International Nuclear Information System (INIS)

    Al-Merey, R.

    2002-04-01

    This study presents two methods for vanadium determination in Syrian commercial phosphoric acid. The vanadium (V) in the oxidized commercial phosphoric acid by ammonium persulfate solution is extracted from 5-M hydrochloride acid medium using N-benzoyl-N-phenyl hydroxyl amine (BPHA) in chloroform as an extracting solution. The first method, the extract vanadium as VOL 2 Cl is changed to V 2 O 3 L 4 complex by the addition of benzimidazole in 1-butanol to the violet organic layer. The absorbance is then measured at 440 nm (the molar absorptivity was found to be 3865 M -1 cm -1 ), where Beer law is applicable up to 36-μg ml -1 . the accuracy, precision and detection limit were found to be 3.7%, 77 ppb and 37 ppb, respectively. the second method, the organic layer is heated to evaporate chloroform, the residue is digested using 20% ammonium persulfate and 2-M sulfuric acid solutions. The vanadium concentration is measured spectrophotometrically by oxidizing gallic acid with persulfate (S 2 O 8 2- ) anion in phosphoric acid medium, where the vanadium (V) acts as a catalyst in the oxidation reaction. This method has a high sensitivity (∼10 -12 ) with accuracy and precision 5% and 0.621 ppb, respectively. Also Beer law at λ m ax=415 nm (ε=∼2 x 10 6 M -1 ) is applicable in the range 2.58-33.3 ppb. (author)

  11. Technology of uranium recovery from wet-process phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Inoue, Katsutoshi [Saga Univ. (Japan). Faculty of Science and Engineering; Nakashio, Fumiyuki

    1982-12-01

    Rock phosphate contains from 0.005 to 0.02 wt.% of uranium. Though the content is a mere 5 to 10 % of that in uranium ore, the total recovery of uranium is significant since it is used for fertilizer manufacture in a large quantity. Wet-process phosphoric acid is produced by the reaction of rock phosphate with sulfuric acid. The recovery of uranium from this phosphoric acid is mostly by solvent extraction at present. According to U/sup 4 +/ or UO/sub 2//sup 2 +/ as the form of its existence, the technique of solvent extraction differs. The following matters are described: processing of rock phosphate; recovery techniques including the extraction by OPPA-octyl pyrophosphoric acid for U/sup 4 +/, and by mixed DEHPA-Di-(2)-ethylhexyl phosphoric acid and TOPO-tryoctyl phosphine oxide for UO/sub 2//sup 2 +/, and by OPAP-octylphenyl acid phosphate for U/sup 4 +/; the recent progress of the technology as seen in patents.

  12. Kinetic study of ion exchange in phosphoric acid chelating resin

    International Nuclear Information System (INIS)

    Brikci-Nigassa, Mounir; Hamouche, Hafida

    1995-11-01

    Uranium may be recovered as a by product of wet phosphoric acid using a method based on specific ion exchange resins. These resins called chelates contain amino-phosphonic functional groups. The resin studied in this work is a purolite S-940; uranium may be loaded on this resin from 30% P2O5 phosphoric acid in its reduced state. The influence of different parameters on the successive steps of the process have been studied in batch experiments: uranium reduction, loading and oxydation. Uranium may be eluted with ammonium carbonate and the resin regeneration may be done with hydrochloric acid.Ferric ions reduce the effective resin capacity considerably and inert fixation conditions are proposed to enhance uranium loading

  13. Extractants for uranium recovery from wet phosphoric acid

    International Nuclear Information System (INIS)

    Musikas, C.; Benjelloun, N.; Lours, S.

    1982-01-01

    Synergistic mixtures containing phosphine oxide plus one of the acidic extractants: dialkyldithiophosphoric acid, dialkylthiophosphoric acid and dialkylphosphoric acid have been compared with respect to U(VI) and Fe(III) extraction from wet phosphoric acid. Distribution curves slope analysis showed that U(VI) extraction mechanisms are totally different. It has been found that U(VI) is extracted as: UO 2 (H 2 PO 4 )(DEHDTP)(TOPO) ; UO 2 (H 2 PO 4 )(DBTP)(POX) 2 and UO 2 (DEHP)(HDEHP) 2 TOPO in dodecane solutions containing di 2 ethylhexyldithiophosphoric acid (HDEHDTP) or dibutylthiophosphoric acid (HDBTP) or di-2-ethylhexylphosphoric acid (HDEHP) plus a phosphine oxide (TOPO or dihexylmethoxyoctylphosphine oxide (POX 11)). The synergistic mixtures containing HDEHDTP gave the highest U(VI) distribution coefficients. Back extraction with oxalic solutions can be achieved only with the synergistic mixtures containing the acidic thiophosphoric donors

  14. Synthesis and complex forming property of phosphor acid derivatives

    International Nuclear Information System (INIS)

    Babaev, B.N.

    2004-01-01

    Full text:With the aim to get new effective and selective extra gents of noble and non-ferrous metals from acid solution and industrial sewage, research of the dependence of 'structure effectiveness' the various phosphor acid derivatives with logical changeable structure (thio phosphor acids, derivatives of dialkoxythiophosphor, O-alkyl-methylphosphon, alkylphenylphosphon, diphenylphosphine acids also 4 methyl-1,3,2 dioxaphosphorinane) which contain different functional groups, the remains of heterocyclic amines and alkaloids, new derivatives of some analytical reagents were synthesized. The structure of synthesized compounds is approved by the results of IR-, PMR-, mass-spectrum analyze. Researching mass-spectrum decay of synthesized phosphor acid derivatives we defined that differing from O-dihexyl-S-propargyl-benzylthio phosphat, mass spectrum decay of O-dialkyl-S-(piperdynobutin-2-il)thio phosphat is characterized by the appearing [M-H] + ions and during the decay ions with high intensiveness are formed. Fragmentation of M + O-alkyl-O-(aminoalkyl)phenylphosphonate proceeds in various directions and characterized with the great number of phosphor containing ions, the possession of the second phenyl radical in the molecule of diphenylphosphon acid derivatives changes the fragmentation of molecular ion of diphenylphosphon acid derivatives. The process of extraction of noble (Au, Ag, Pt, Pd, Os) metals from hydrochloric-sulphur-nitrogen acid medium was analyzed by radioactive indicator's method. It was noticed that structure, strength, conformation of compounds, the temperature, of acid medium (0,1-10 M) and the nature of acids (HCL, H 2 SO 4 , HNO 3 ) could have strong influence to the effectiveness of metal extraction. During the research of metals extraction from pure solutions we can see the followings: 1) There are such substances, which can be used as effective group reagent towards the Au, Ag and Pd. 2) Derivatives with acetylene extract ions of gold from

  15. 40 CFR 721.6200 - Fatty acid polyamine condensate, phosphoric acid ester salts.

    Science.gov (United States)

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Fatty acid polyamine condensate... New Uses for Specific Chemical Substances § 721.6200 Fatty acid polyamine condensate, phosphoric acid... substances identified as fatty acid polyamine condensate, phosphate ester salts (PMNs P-90-1984 and P-90-1985...

  16. Process for recovering uranium from wet process phosphoric acid (III)

    International Nuclear Information System (INIS)

    Pyrih, R.Z.; Rickard, R.S.; Carrington, O.F.

    1983-01-01

    Uranium is conventionally recovered from wet-process phosphoric acid by two liquid ion exchange steps using a mixture of mono- and disubstituted phenyl esters of orthophosphoric acid (OPPA). Efficiency of the process drops as the mono-OPPA is lost preferentially to the aqueous phase. This invention provides a process for the removal of the uranium process organics (OPPA and organic solvents) from the raffinate of the first liquid ion exchange step and their return to the circuit. The process organics are removed by a combination flotation and absorption step, which results in the recovery of the organics on beads of a hydrophobic styrene polymer

  17. Process for extracting uranium from phosphoric acid solutions

    International Nuclear Information System (INIS)

    1977-01-01

    The description is given of a method for extracting uranium from phosphoric acid solutions whereby the previously oxided acid is treated with an organic solvent constituted by a mixture of dialkylphosphoric acid and trialkylphosphine oxide in solution in a non-reactive inert solvent so as to obtain de-uraniated phosphoric acid and an organic extract constituted by the solvent containing most of the uranium. The uranium is then separated from the extract as uranyl ammonium tricarbonate by reaction with ammonia and ammonium carbonate and the extract de-uraniated at the extraction stage is recycled. The extract is treated in a re-extraction apparatus comprising not less than two stages. The extract to be treated is injected at the top of the first stage. At the bottom of the first stage, ammonia is introduced counter current as gas or as an aqueous solution whilst controlling the pH of the first stage so as to keep it to 8.0 or 8.5 and at the bottom of the last stage an ammonium carbonate aqueous solution is injected in a quantity representing 50 to 80% of the stoichiometric quantity required to neutralize the dialkylphosphoric acid contained in the solvent and transform the uranium into uranyl ammonium tricarbonate [fr

  18. Absorption characteristics of Kupravas deposit clays modified by phosphoric acid

    International Nuclear Information System (INIS)

    Ruplis, A.; Mezinskis, G.; Chaghuri, M.

    1998-01-01

    Literature data suggested that clays may be used as sorbents for waste water treatment. The surface and sorption properties of minerals changes due to the influence of acid rains. The process of recession of clay properties has been modeled in laboratory by treatment of clays with mineral acids at higher temperature that in natural conditions. The present paper is devoted to the study of influence of phosphoric acid on the sorption properties of Kupravas deposit clays. Natural clay samples and samples treated with phosphoric acid were characterized by means of x-ray diffraction an differential thermal analysis (DTA) methods These methods were used also to identify the sample of Lebanese clays. X-ray diffraction analysis data show that the samples of clays from the deposit of Kuprava contain illite and kaolinite while sample of Lebanese clay contains quartz, calcite, and montmorillonite. DTA results show characteristic features of Kuprava clays described in reference with DTA of Lebanese clay clearly demonstrate the presence of large quantity of calcite

  19. Nitric-phosphoric acid oxidation of organic waste materials

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  20. Ionic flotation of uranium contained in industrial phosphoric acid

    International Nuclear Information System (INIS)

    Jdid; Blazy; Bessiere

    1983-01-01

    A new process for uranium recovery from industrial phosphoric acid at 30% of P 2 O 5 is applied by the ionic flotation process. Research is carried out on determination of the nature of ionic species of U in H 3 PO 4 5.5 M and the behavior of reagents from CECA Co. in very acid media. Reagents able to form complexes directly with uranium and stable in phosphoric acid selected are: potassium ethylene diamine tetra (methylene phosphonate) (INIPOL AD32) and sodium dialkyldiphosphonate (34S). Uranium IV, obtained by reduction of uranium VI with iron powder, is precipitated by these reagents. Flotation of the precipitate obtained with INIPOL AD 32 is realized by addition of hexylamino bis (methylene phosphonic acid). A recovery of 80 wt% is obtained. Flotation of the coprecipitate 34S-U(IV) is obtained without any other additions because 34S is a surfactant. Metal recovery is better than 90% and the coprecipitate contains more than 10% U. The process is fast precipitation 10 minutes and flotation 5 minutes and is efficient even at 60 0 C [fr

  1. Recovering of uranium from phosphoric acid produced by the wet process

    International Nuclear Information System (INIS)

    Barreiro, A.J.; Lyon, W.L.; Holleman, R.A.; Randell, C.C.

    1977-01-01

    Process for recovering uranium as from an aqueous solution of phosphoric acid arising from a wet process, with a scrubbing agent essentially composed of a hydrocarbon whose boiling point is situated between 150 0 C and 300 0 C, which reacts with the contaminents formed in the sludge in the phosphoric acid, in an efficient enough quantity to wash the contamination products forming the phosphoric acid sludge, give a sludge phase and a purified phosphoric acid phase, after which the sludge phase is extracted [fr

  2. Process for recovering uranium from wet process phosphoric acid

    International Nuclear Information System (INIS)

    Pyrih, R.Z.; Rickard, S.; Carrington, F.

    1982-01-01

    A process for recovering uranium from phosphoric acid solutions uses an acidified alkali metal carbonate solution for the second-stage strip of uranyl uranium from the ion-exchange solution. The stripped solution is then recycled to the ion-exchange circuit. In the first stripping stage the ion-exchange solution containing the recovered uranyl uranium and an inert organic diluent is stripped with ammonium carbonate, producing a slurry of ammonium uranyl tricarbonate. The second strip, with a solution of 50-200 grams per litre of sodium carbonate eliminates the problems of inadequate removal of phosphorus, iron and vanadium impurities, solids accumulation, and phase separation in the strip circuit

  3. The optimisation study of tbp synthesis process by phosphoric acid

    International Nuclear Information System (INIS)

    Amedjkouh, A.; Attou, M.; Azzouz, A.; Zaoui, B.

    1995-07-01

    The present work deals with the optimisation study of TBP synthesis process by phosphoric acid. This way of synthesis is more advantageous than POCL3 or P2O5 as phosphatant agents. these latters are toxic and dangerous for the environnement. The optimisation study is based on a series of 16 experiences taking into account the range of variation of the following parameters : temperature, pressure, reagents mole ratio, promoter content. the yield calculation is based on the randomisation of an equation including all parameters. the resolution of this equation gave a 30% TBP molar ratio. this value is in agreement with that of experimental data

  4. Alternative processes for uranium recovery from phosphoric acid

    International Nuclear Information System (INIS)

    Duarte Neto, J.; Santos Benedetto, J. dos; Aquino, J.A. de

    1987-01-01

    Two processes of solvent extraction using D 2 EHPATOPO synergistic mixture, in order to recover uranium from phosphoric acid proceeding from physical and chemical treatments of the phosphorus-uraniferous ore of Itataia-CE, Brazil, are studied. The steps of each process were studied in laboratory and pilot scales. The flow charts for both processes with detailed description of each step, the operational conditions, the mass balances, the results obtained and the description of pilot units, are presented. (M.C.K.) [pt

  5. Separation of uranium from molybdenum by alkyl phosphoric acid extraction

    Energy Technology Data Exchange (ETDEWEB)

    Zhongshi, Li

    1986-08-01

    The regularities of separation of uranium from molybdenum by alkyl phosphoric acid extraction are described. Two parameters, i.e., density ratio of uranium to molybdenum in organic phase at first stage and density of uranium in raffinate at last stage are presented. The relationship between these parameters and purity of molybdenum and uranium products is given. The method of adjusting and controlling these parameters in experiments and production is worked out. The technical key problem in comprehensive utilization of sedimentary type uranium ore containing molybdenum with close concentration of these to elements has been solved.

  6. Complexity in Acid?Base Titrations: Multimer Formation Between Phosphoric Acids and Imines

    OpenAIRE

    Malm, Christian; Kim, Heejae; Wagner, Manfred; Hunger, Johannes

    2017-01-01

    Abstract Solutions of Br?nsted acids with bases in aprotic solvents are not only common model systems to study the fundamentals of proton transfer pathways but are also highly relevant to Br?nsted acid catalysis. Despite their importance the light nature of the proton makes characterization of acid?base aggregates challenging. Here, we track such acid?base interactions over a broad range of relative compositions between diphenyl phosphoric acid and the base quinaldine in dichloromethane, by u...

  7. A process for uranium recovery in phosphoric acid

    International Nuclear Information System (INIS)

    Duarte Neto, J.

    1984-01-01

    Results are presented about studies carried out envisaging the development of a process for uranium recovery from phosphoric acid, produced from the concentrate obtained from phosphorus-uraniferous mineral from Itataia mines (CE, Brazil). This process uses a mixture of DEPA-TOPO as extractant and the extraction cycle involves the following stages: acid pre-treatment; adjustment of the oxidation potential so to ensure that all uranium is hexavalent; extraction of uranium from the acid; screening of the solvent to remove undesirable impurities; uranium re-extraction and precipitation; solvent recovery. A micro-pilot plant for continuous processing was built up. Data collected showed that uranium can be recovered with an yield greater than 99%, thus proving the feasibility of the process and encouraging the construction of a bigger scale plant. (Author) [pt

  8. Radiotracer investigation of phosphoric acid and phosphatic fertilizers production process

    International Nuclear Information System (INIS)

    Ben Abdelouahed, H.; Reguigui, N.

    2011-01-01

    In the phosphoric acid production process, the time a particle spends inside the chemical reactor (residence time) is of paramount importance to process engineers. Residence time distribution (RTD) gives information on the efficiency of the chemical reactor, on the efficiency of the process, and also the availabilities of the reactive volume for the reaction (active volume vs. dead volume). Traditionally, chemical engineers used chemical tracer to determine the RTD. However, first disadvantage is that the chemical tracer could not allow an online diagnosis: the samples containing chemical tracer have to go to a lab for analysis, second disadvantage is that the chemical tracer is less sensitive than radioactive ones because of its adsorption onto strata or its retention in rocks. Consequently, chemical tracer results are not always precise and cannot convincingly explain the multiple flow-path model. Radioactive tracers are the only tracers capable of measuring the active RTD with high degree of precision and give information on the internal recirculation rate. In this work, we will describe the application of radiotracer method for RTD measurement in the phosphoric acid production process and give results and discussion of each case encountered. (author)

  9. Radioactivity Content in Phosphoric Acid Used for Fertilizer Production

    International Nuclear Information System (INIS)

    Ibrahiem, N.M.; Hamed, A.A.

    2003-01-01

    Uranium content in phosphoric acid used fertilizer production was measured by alpha spectrometry, laser fluorimetry high resolution gamma spectrometry. Also, polonium-210 content was determined in phosphoric acid by alpha spectrometry. Uranium-234 and uranium-238 concentrations, measured by alpha spectroscopy, were found to be 601 and 507 Bq I -1 , respectively. Total uranium content obtained by laser fluorimetry was about 545 BqI - (45.4ppm). Gamma spectroscopy analysis gave the concentrations of 40 K, 238 U, 235 U, 214 Pb, 214 Bi and 208 TI, as 17,644,19.5, 1.2,1.3 and 9.4 Bq I -1 , respectively. Polonium-210 concentration was found to be about 3.1 Bq I -1 . Uranium-232 and polonium-208 were used as yield tracers, for alpha measurements of uranium and polonium, respectively. Samples of the tri-super phosphate (TSP) and single-super phosphate (SSP) fertilizers and the phosphogypsum produced were also analyzed by gamma spectroscopy. Uranium content in both phosphate fertilizers was 3205 and 1440 Bq Kg -1 for 238 U and 83 and 35 Bq Kg -1 for, 235 U respectively

  10. Online Automatic Titration of Chromic Acid in Chromium Plating Solutions and Phosphoric and Sulfuric Acids in Electropolishing Solutions

    National Research Council Canada - National Science Library

    Sopok, Samuel

    1991-01-01

    .... The analytical chemistry literature lacks an adequate online automatic titration method for the monitoring of chromic acid in chromium plating solutions and the monitoring of phosphoric and sulfuric...

  11. SEPARATION OF p-AMINOBENZOIC ACID BY REACTIVE EXTRACTION. 1. MECHANISM AND INFLUENCING FACTORS

    Directory of Open Access Journals (Sweden)

    DAN CASCAVAL

    2008-09-01

    Full Text Available The comparative study on the reactive extraction of p-aminobenzoic acid with Amberlite LA-2 and D2EHPA in two solvents with different polarity (n-heptane and dichloromethane indicated that the extractant type and solvent polarity control the extraction mechanism. Thus, the reactive extraction with Amberlite LA-2 occurs by means of the interfacial formation of an aminic adduct with three extractant molecules in low-polar solvent, or of an salt with one extractant molecule in higher polar solvent. Similarly, the extraction with D2EHPA is based on the formation of an acidic adduct with two extractant molecules in n-heptane, or of a salt with one extractant molecule in dichloromethane. The most efficient extraction has been reached for the combination Amberlite LA-2-dichloromethane.

  12. Uranium recovery from wet-process phosphoric acid with octylphenyl acid phosphate. Progress report

    International Nuclear Information System (INIS)

    Arnold, W.D.; McKamey, D.R.; Baes, C.F.

    1980-01-01

    Studies were continued of a process for recovering uranium from wet-process phosphoric acid with octylphenyl acid phosphate (OPAP), a mixture of mono- and dioctylphenyl phosphoric acids. The mixture contained at least nine impurities, the principal one being octyl phenol, and also material that readily hydrolyzed to octyl phenol and orthophosphoric acid. The combination of mono- and dioctylphenyl phosphoric acids was the principal uranium extractant, but some of the impurities also extracted uranium. Hydrolysis of the extractant had little effect on uranium extraction, as did the presence of moderate concentrations of octyl phenol and trioctylphenyl phosphate. Diluent choice among refined kerosenes, naphthenic mixtures, and paraffinic hydrocarbons also had little effect on uranium extraction, but extraction was much lower when an aromatic diluent was used. Purified OPAP fractions were sparingly soluble in aliphatic hydrocarbon diluents. The solubility was increased by the presence of impurities such as octyl phenol, and by the addition of water or an acidic solution to the extractant-diluent mixture. In continuous stability tests, extractant loss by distribution to the aqueous phase was much less to wet-process phosphoric acid than to reagent grade acid. Uranium recovery from wet-process acid decreased steadily because of the combined effects of extractant poisoning and precipitation of the extractant as a complex with ferric iron. Unaccountable losses of organic phase volume occurred in the continuous tests. While attempts to recover the lost organic phase were unsuccessful, the test results indicate it was not lost by entrainment or dissolution in the phosphoric acid solutions. 21 figures, 8 tables

  13. Process for the winning of a concentrate containing uranium and purified phosphoric acid, as well as the concentrate containing uranium and purified phosphoric acid obtained by this process

    International Nuclear Information System (INIS)

    1980-01-01

    The uranium containing concentrate and purified phosphoric acid are obtained by treating wet phosphoric acid with an inorganic fluorine compound (ammonium fluoride) and an aliphatic ketone (acetone) in the presence of a reducing agent (finely divided iron). The ketone is added first and the formed uranium precipitate is separated from the solution. If the fluorine compound is added first, the yield is lowered by a factor of 2. (Th.P.)

  14. Study of the mechanism and kinetics of the reduction of uranyl ions in phosphoric acid solutions

    International Nuclear Information System (INIS)

    El Kacemi, K.; Tyburce, B.; Belcadi, S.

    1982-01-01

    The electrochemical reduction of uranyl ions in 0.1 to 9 M phosphoric acid has been investigated by polarography, cyclic voltammetry, chronopotentiometry and potentiostatic coulometry. In concentrated phosphoric acid solutions (H 3 PO 4 3 PO 4 concentrations. So, when the concentration of U(VI) increases and/or that of H 3 PO 4 reduces, the system becomes reversible. (author)

  15. Continuous tests of Phosphoric Acid - dihydrate process - from phosphatic concentrate of Itataia-CE ore

    International Nuclear Information System (INIS)

    Santos Benedetto, J. dos.

    1984-01-01

    A consolidation of principal studies and continuous tests done with phosphatic concentrated of Itataia ore intending phosphoric acid production by humid-route dihydrate way process is presented. The production of phosphoric acid is applied in uranium extraction process by solvents. (author) [pt

  16. Determination of the activity concentration of 230Th in phosphoric acids produced in Brazil

    International Nuclear Information System (INIS)

    Taddei, M.H.T.; Ferreira, M.T.; Fukuma, H.T.; Xavier, T.T.; Sousa, F.V.T.S.

    2017-01-01

    The high uranium phosphate rock from Itataia, Brazil, was processed using the wet route in the dihydrate system to manufacture phosphoric acid. The uranium contained in phosphoric acid was recovered by the solvent extraction technique. The distribution of the long half-life radionuclides from the decay series of 238 U and 232 Th were evaluated in these processes. The 26 Ra, 228 Ra and 210 Pb radionuclides were found predominantly in phosphogypsum, while the isotopes of 228 Th, 230 Th and 232 Th predominated in phosphoric acid after extracting uranium. The main concern in the commercialization of phosphoric acid that will be produced in the Itataia plant is in relation to the content of 230 Th. This work determined the content of these radionuclides in phosphoric acid from different locations in the country in order to compare

  17. Application of a precipitation method for uranium recovery from Abu-Zaabal phosphoric acid plant, egypt

    International Nuclear Information System (INIS)

    El-Hazek, N.M.T.; Hussein, E.M.

    1997-01-01

    Current industrial recovery of uranium from 30% phosphoric acid-produced by the dihydrate process-is based on solvent extraction method. Uranium recovery from concentrated phosphoric acid (45-52% P 2 O 5 ) produced by evaporation of the 30% acid or directly produced by the hemihydrate process, by solvent extraction is difficult to apply in practice. In addition to possible contamination of the acid by the organic solvents and/or their deterioration. This paper investigates the possibility of applying a precipitation method (Weterings and Janssen, 1985) for uranium recovery from both low (28% P 2 O 2 ) and high (48% P 2 O 5 ) concentration phosphoric acids produced by abu-Zaabal phosphoric acid plant (abu-Zaabal fertilizers and chemicals Co., Egypt). The 28% acid produced by H 2 SO 4 dihydrate method and the 48% acid produced by evaporation of the 28% acid

  18. Extraction of uranium from phosphoric-hydrobromic acid mixture by N-lauryl tri alkyl methylamine

    Energy Technology Data Exchange (ETDEWEB)

    Guirguis, L A [Nuclear materials authority, Cairo, (Egypt); Tadros, N A [Hot laboratories center, atomic energy authority, Cairo, (Egypt)

    1995-10-01

    A uranium recovery process from phosphoric acid produced by the dihydrate method was elaborated. Decomposition of phosphate rock containing 0.02% U is carried out with sulphuric acid. Crude phosphoric acid is filtered off, steam concentrated to 45% P{sub 2} O{sub 5} (6.27 M) and then clarified with activated clay and carbon. The clear phosphoric acid is introduced to uranium extraction after the addition of 0.88 M hydrobromic acid by 0.134 M amberlite LA.2 and 5% decanol, as a modifier, in kerosene. While 10% ammonium sulphate solution is used for stripping. Over 90% uranium recovery is obtained. 6 figs., 1 tab.

  19. Initiation in the study of uranium recovery from the phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Anchondo Adalid, J M

    1974-01-01

    The loss of considerable amounts of uranium in the Mexican phosphoric acid industry makes it important to study economic methods of recovery; the studies can serve as a basis for the construction and operation of a pilot plant as a normal preliminary to larger-scale projects. Routine experimental techniques for solvent extraction were employed. Extraction efficiencies of the order of 90-95% were obtained using 0.09-0.18M solutions of a mixture of phosphoric octyl esters applied to 4 and 6M solutions of phosphoric acid (reagent grade) containing uranium in concentrations of 0.05-0.50g of U/sub 3/O/sub 8/ per litre of acid. The conclusion was reached that phosphoric octyl esters can be used for recovering uranium in satisfactory quantities from phosphoric acid solutions by means of solvent extraction, and that the uranium can be separated from the solvent by the established procedures.

  20. Initiation in the study of uranium recovery from the phosphoric acid

    International Nuclear Information System (INIS)

    Anchondo Adalid, J.M.

    1974-01-01

    The loss of considerable amounts of uranium in the Mexican phosphoric acid industry makes it important to study economic methods of recovery; the studies can serve as a basis for the construction and operation of a pilot plant as a normal preliminary to larger-scale projects. Routine experimental techniques for solvent extraction were employed. Extraction efficiencies of the order of 90-95% were obtained using 0.09-0.18M solutions of a mixture of phosphoric octyl esters applied to 4 and 6M solutions of phosphoric acid (reagent grade) containing uranium in concentrations of 0.05-0.50g of U 3 O 8 per litre of acid. The conclusion was reached that phosphoric octyl esters can be used for recovering uranium in satisfactory quantities from phosphoric acid solutions by means of solvent extraction, and that the uranium can be separated from the solvent by the established procedures. (author)

  1. Phosphorous gettering in acidic textured multicrystalline solar cells

    Energy Technology Data Exchange (ETDEWEB)

    Montesdeoca-Santana, A. [Departamento de Fisica Basica, Universidad de La Laguna (ULL), Avenida Astrofisico Francisco Sanchez 2, 38206 La Laguna, S/C de Tenerife (Spain); Fraunhofer Institut fuer Solare Energiesysteme ISE, Laboratory and Servicecenter Gelsenkirchen, Auf der Reihe 2, 45884 Gelsenkirchen (Germany); Jimenez-Rodriguez, E.; Diaz-Herrera, B.; Hernandez-Rodriguez, C. [Departamento de Fisica Basica, Universidad de La Laguna (ULL), Avenida Astrofisico Francisco Sanchez 2, 38206 La Laguna, S/C de Tenerife (Spain); Gonzalez-Diaz, B. [Departamento de Fisica Basica, Universidad de La Laguna (ULL), Avenida Astrofisico Francisco Sanchez 2, 38206 La Laguna, S/C de Tenerife (Spain); Departamento de Energia Fotovoltaica, Instituto Tecnologico y de Energias Renovables. Poligono Industrial de Granadilla s/n, 38600 San Isidro-Granadilla de Abona, S/C de Tenerife (Spain); Rinio, M.; Borchert, D. [Fraunhofer Institut fuer Solare Energiesysteme ISE, Laboratory and Servicecenter Gelsenkirchen, Auf der Reihe 2, 45884 Gelsenkirchen (Germany); Guerrero-Lemus, R. [Departamento de Fisica Basica, Universidad de La Laguna (ULL), Avenida Astrofisico Francisco Sanchez 2, 38206 La Laguna, S/C de Tenerife (Spain); Fundacion de Estudios de Economia Aplicada, Catedra Focus-Abengoa, Jorge Juan 46, 28001 Madrid (Spain)

    2011-03-15

    The influence of phosphorus gettering is studied in this work applied to an acidic textured multicrystalline silicon substrate. The texturization was achieved with an HF/HNO{sub 3} solution leading to nanostructures on the silicon surface. It has been demonstrated in previous works that this textured surface decreases the reflectance on the solar cell and increases the surface area improving the photon collection and enhancing the short circuit current. The present study investigates the effect on the minority carrier lifetime of the phosphorous diffusion when it is carried out on this textured surface. The lifetime is measured by means microwave photoconductance decay and quasi steady state phototoconductance devices. The diffused textured wafers are used to fabricate solar cells and their electrical parameters are analyzed. (copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  2. Woking Park phosphoric acid fuel cell CHP monitoring

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2005-09-15

    A phosphoric acid fuel (PC25) delivering up to 200kw of electrical power and commensurate heat was installed in Woking Park UK in late 2006 and has been monitored over a period of one year. The system supplies electric power to a leisure centre and swimming pool via a private wires network. This report gives details of the monitoring and shows a schematic of the system, data on electrical and thermal efficiencies, stack voltage variations and gaseous emissions. Extended monitoring is now taking place to provide a complete picture of the economics and operation of the fuel cell in the developing combined heat and power unit and private wires system. The contractor is Advantica of Loughborough and detailed results of the monitoring are available on the DTI website.

  3. Procedure for recovery from an uranium containing concentrate and phosphoric acid, as well as an uranium containing concentrate and phosphoric acid obtained by this procedure

    International Nuclear Information System (INIS)

    1980-01-01

    The phosphate ore is dissolved in sulphuric acid and the formed calcium sulphate is separated from the solution. The uranium is then precipitated by adding ammonium fluoride solution to the remaining phosphoric acid solution. When the phosphate ore is dissolved in sulphuric acid, fluorine gas is liberated and this is then used to produce the ammonium fluoride solution. (Th.P.)

  4. Oxidizer in phosphoric reactors

    International Nuclear Information System (INIS)

    Santos Benedetto, J. dos

    1985-01-01

    Oxidation during the manufacture of wet-process phosphoric acid affected the distribution of uranium and impurities between phosphoric acid and gypsum, by decreasing the uranium loss to gypsum and the impurities solubilization in phosphoric acid. (Author) [pt

  5. Determination of anions in pure and commercial phosphoric acid by ion chromatography and manual of 792 basic IC

    International Nuclear Information System (INIS)

    Al-Kabani, F.; Abdulbaki, M. K.

    2007-01-01

    A method for determination of anions in pure and concentrated phosphoric and samples (85%) and commercial phosphoric acid ion chromatography was developed, in order to control the specification of phosphoric acid produced in the pilot plant for phosphoric acid purification. The accuracy of the method was studied and the standard deviation was found to be between 0.09 and 0.10. Operation instructions of 792 Basic IC was described. (author)

  6. Hydrometallurgical process for the recovery of metal values from spent lithium-ion batteries in citric acid media.

    Science.gov (United States)

    Chen, Xiangping; Zhou, Tao

    2014-11-01

    In this paper, a hydrometallurgical process has been proposed to recover valuable metals from spent lithium-ion batteries in citric acid media. Leaching efficiencies as high as 97%, 95%, 94%, and 99% of Ni, Co, Mn, and Li were achieved under the optimal leaching experimental conditions of citric acid concentration of 2 mol L(-1), leaching temperature of 80 °C, leaching time of 90 min, liquid-solid ratio of 30 ml g(-1), and 2 vol. % H2O2. For the metals recovery process, nickel and cobalt were selectively precipitated by dimethylglyoxime reagent and ammonium oxalate sequentially. Then manganese was extracted by Na-D2EHPA and the manganese-loaded D2EHPA was stripped with sulfuric acid. The manganese was recovered as MnSO4 in aqueous phase and D2EHPA could be reused after saponification. Finally, lithium was precipitated by 0.5 mol L(-1) sodium phosphate. Under their optimal conditions, the recovery percentages of Ni, Co, Mn, and Li can reach 98%, 97%, 98%, and 89%, respectively. This is a relatively simple route in which all metal values could be effectively leached and recovered in citric acid media. © The Author(s) 2014.

  7. Spectrophotometric Analysis of Phosphoric Acid Leakage in High-Temperature Phosphoric Acid-Doped Polybenzimidazole Membrane Fuel Cell Application

    Directory of Open Access Journals (Sweden)

    Seungyoon Han

    2016-01-01

    Full Text Available High-temperature proton exchange membrane fuel cells (HT-PEMFCs utilize a phosphoric acid- (PA- doped polybenzimidazole (PBI membrane as a polymer electrolyte. The PA concentration in the membrane can affect fuel cell performance, as a significant amount of PA can leak from the membrane electrode assembly (MEA by dissolution in discharged water, which is a byproduct of cell operation. Spectrophotometric analysis of PA leakage in PA-doped polybenzimidazole membrane fuel cells is described here. This spectrophotometric analysis is based on measurement of absorption of an ion pair formed by phosphomolybdic anions and the cationoid color reagent. Different color reagents were tested based on PA detection sensitivity, stability of the formed color, and accuracy with respect to the amount of PA measured. This method allows for nondestructive analysis and monitoring of PA leakage during HT-PEMFCs operation.

  8. Complexity in Acid-Base Titrations: Multimer Formation Between Phosphoric Acids and Imines.

    Science.gov (United States)

    Malm, Christian; Kim, Heejae; Wagner, Manfred; Hunger, Johannes

    2017-08-10

    Solutions of Brønsted acids with bases in aprotic solvents are not only common model systems to study the fundamentals of proton transfer pathways but are also highly relevant to Brønsted acid catalysis. Despite their importance the light nature of the proton makes characterization of acid-base aggregates challenging. Here, we track such acid-base interactions over a broad range of relative compositions between diphenyl phosphoric acid and the base quinaldine in dichloromethane, by using a combination of dielectric relaxation and NMR spectroscopy. In contrast to what one would expect for an acid-base titration, we find strong deviations from quantitative proton transfer from the acid to the base. Even for an excess of the base, multimers consisting of one base and at least two acid molecules are formed, in addition to the occurrence of proton transfer from the acid to the base and simultaneous formation of ion pairs. For equimolar mixtures such multimers constitute about one third of all intermolecular aggregates. Quantitative analysis of our results shows that the acid-base association constant is only around six times larger than that for the acid binding to an acid-base dimer, that is, to an already protonated base. Our findings have implications for the interpretation of previous studies of reactive intermediates in organocatalysis and provide a rationale for previously observed nonlinear effects in phosphoric acid catalysis. © 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.

  9. Radionuclide concentrations in raw and purified phosphoric acids from Brazil and their processing wastes: implications for radiation exposures.

    Science.gov (United States)

    da Conceição, Fabiano Tomazini; Antunes, Maria Lúcia Pereira; Durrant, Steven F

    2012-02-01

    Radionuclides from the U and Th natural series are present in alkaline rocks, which are used as feedstock in Brazil for the production of raw phosphoric acid, which can be considered as a NORM (naturally occurring radioactive material). As a result of the purification of raw phosphoric acid to food-grade phosphoric acid, two by-products are generated, i.e., solid and liquid wastes. Taking this into account, the main aim of this study was to evaluate the fluxes of natural radionuclide in the production of food-grade phosphoric acids in Brazil, to determine the radiological impact caused by ingestion of food-grade phosphoric acid, and to evaluate the solid waste environmental hazards caused by its application in crop soils. Radiological characterization of raw phosphoric acid, food-grade phosphoric acid, solid waste, and liquid waste was performed by alpha and gamma spectrometry. The (238)U, (234)U, (226)Ra, and (232)Th activity concentrations varied depending on the source of raw phosphoric acid. Decreasing radionuclides activity concentrations in raw phosphoric acids used by the producer of the purified phosphoric acid were observed as follows: Tapira (raw phosphoric acid D) > Catalão (raw phosphoric acids B and C) > Cajati (raw phosphoric acid A). The industrial purification process produces a reduction in radionuclide activity concentrations in food-grade phosphoric acid in relation to raw phosphoric acid produced in plant D and single raw phosphoric acid used in recent years. The most common use of food-grade phosphoric acid is in cola soft drinks, with an average consumption in Brazil of 72 l per person per year. Each liter of cola soft drink contains 0.5 ml of food-grade phosphoric acid, which gives an annual average intake of 36 ml of food-grade phosphoric acid per person. Under these conditions, radionuclide intake through consumption of food-grade phosphoric acid per year per person via cola soft drinks is not hazardous to human health in Brazil

  10. Flocculation of suspended matter in a crude wet phosphoric acid (Algeria)

    International Nuclear Information System (INIS)

    Brikci Nigassa, M.; Bensebaa, A.

    1994-11-01

    Prior to the recovery of uranium, a pre-treatment of the phosphoric acid is necessary to remove soluble impurities of different origins. In this work, synthetic flocculants have been used. the influence of operating conditions on flocculation and filtration, such as, type of flocculants, polymer concentration, temperature, mixing and time of agitation, has been studied for both aged and fresh phosphoric acid. It has been shown that synthetic flocculants can be used for flocculation ins a phosphoric acid medium and that flocculation and filtration processes are strongly linked

  11. Method for separating mono- and di-octylphenyl phosphoric acid esters

    International Nuclear Information System (INIS)

    Arnold, W.D. Jr.

    1977-01-01

    A method for separating mono-octylphenyl phosphoric acid ester and di-octylphenyl phosphoric acid ester from a mixture thereof comprises reacting the ester mixture with a source of lithium or sodium ions to form a mixture of the phosphate salts; contacting the salt mixture with an organic solvent which causes the dioctylphenyl phosphate salt to be dissolved in the organic solvent phase and the mono-octylphenyl phosphate salt to exist in a solid phase; separating the phases; recovering the phosphate salts from their respective phases; and acidifying the recovered salts to form the original phosphoric acid esters

  12. Uranium problem in production of wet phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Gorecka, H; Gorecki, H [Politechnika Wroclawska (Poland)

    1980-01-01

    The balance of the uranium in the wet dihydrate method was presented. This balance shows that a large quantity of the uranium compounds shift from mineral phosphate rock to liquid phase of decomposition pulp (about 70-85% U) and the rest moves to phosphogypsum (about 15-25% U). The contents of uranium in phosphate rock imported for our country and in products and by-products of the fertilizer industry, were determined. Concentration of uranium in the phosphogypsum is dependent on the type of mineral rock and the process of phosphogypsum crystallization. Analysis of the uranium contents in phosphogypsum samples and results of the sedimentation analysis indicated influence of the specific surface of phosphogypsum crystals on the uranium concentration. Investigation of the sets of samples obtained in the industrial plant proved that phosphogypsum cake washed counter-currently on the filter contained from 10 to 20 ..mu..g U/g. The radioactivity of these samples fluctuated from 35 to 60 pCi/g. Using solution sulphuric acid of concentration in range 2-4% by weight H/sub 2/SO/sub 4/ to washing and repulpation of the phosphogypsum enables to reduce its radioactivity to level below 25 pCi/g. This processing makes possible to utilize this waste material in the building industry. Extraction of uranium from the wet phosphoric acid using kerosen solution of the reaction product between octanol -1 and phosphorus pentaoxide showed possibility to recover over 80% of uranium contained in phosphate rock.

  13. Promotion of Crystal Growth on Biomass-based Carbon using Phosphoric Acid Treatments

    Directory of Open Access Journals (Sweden)

    Liwei Yu

    2015-02-01

    Full Text Available The effect of phosphoric acid treatments on graphitic microcrystal growth of biomass-based carbons was investigated using X-ray diffraction, infrared spectroscopy, and Raman spectroscopy. Although biomass-based carbons are believed to be hard to graphitize even after heat treatments well beyond 2000 °C, we found that graphitic microcrystals of biomass-based carbons were significantly promoted by phosphoric acid treatments above 800 °C. Moreover, twisted spindle-like whiskers were formed on the surface of the carbons. This suggests that phosphorus-containing groups turn graphitic microcrystalline domains into graphite during phosphoric acid treatments. In addition, the porous texture of the phosphoric acid-treated carbon has the advantage of micropore development.

  14. Recent studies of uranium recovery from wet-process phosphoric acid with octylphenyl acid phosphate

    International Nuclear Information System (INIS)

    Arnold, W.D.

    1978-01-01

    Commercial OPAP is a complex mixture that contains at least 11 components. Octyl phenol is the principal impurity. Commercial OPAP contains readily-hydrolyzable material. The concentrations of octyl phenol and an unidentified impurity increase in the hydrolyzed product. Uranium extraction power is decreased slightly by hydrolysis of the reagent. Four major problems were encountered in continuous stability tests: (1) Microemulsion or micelle formation--loss of organic phase into phosphoric acid. We do not have a solution to this problem at this time. It could involve alteration of the organic, e.g., adding a modifier, changing the reagent structure, or changing the diluent. (2) Reagent poisoning--reduction of uranium extraction and interference with organic titrations by material extracted from the acid. Additional work is needed to identify the poisoning material or materials. It can then be removed if it originates in the phosphate rock, or avoided if it originates in chemicals added during processing. (3) Crystallization with iron--loss of both major components of the reagent as a complex with ferric iron. We believe this problem can be controlled by controlling the ferric iron concentration in the phosphoric acid. (4) MOPPA distribution loss--a selective loss to the aqueous phase. We believe this can be minimized by controlling the iron concentration of the phosphoric acid. The iron concentration will need to be kept low enough to avoid reagent crystallization and high enough to avoid MOPPA distribution loss. 15 figs

  15. Oxidation-extraction of uranium from wet-process phosphoric acid

    International Nuclear Information System (INIS)

    Lawes, B.C.

    1985-01-01

    The invention involves an improvement to the reductive stripping process for recovering uranium values from wet-process phosphoric acid solution, where uranium in the solution is oxidized to uranium (VI) oxidation state and then extracted from the solution by contact with a water immiscible organic solvent, by adding sufficient oxidant, hydrogen peroxide, to obtain greater than 90 percent conversion of the uranium to the uranium (VI) oxidation state to the phosphoric acid solution and simultaneously extracting the uranium (VI)

  16. Determination of formal potential of Amsup((4))/Amsup((3)) pair in phosphoric-acid solutions

    International Nuclear Information System (INIS)

    Mikhajlov, V.M.; Myasoedov, B.F.

    1977-01-01

    Values of formal potentials of the system Amsup((4))/Amsup((3)) in 12 and 15 M phosphoric acid at 20+-2 deg C are determined by potentiometric method. The effect is studied of metallic platinum on the process of self-reduction of tetravalent americium, and the optimum conditions are found for potentiostatic oxidation of Amsup((3)) to Amsup((4)) in 12 M phosphoric acid

  17. The use of ion chromatography for the determination of impurities in crude phosphoric acid

    International Nuclear Information System (INIS)

    Pires, M.A.F.; Atalla, L.T.; Abrao, A.

    1988-07-01

    The determination of fluoride, nitrate, sulphate and phosphate ions in crude phosphoric acid by means of ion chromatography is described. A previous separation of interferent cations was made by using a cationic resin or EDTA complexation. The last alternative allowed more reproductible results. The technique described is very quick and is being applied for the simultaneous determination of impurities in phosphoric acid and its own phosphospate concentration. The method is quick and has good reprodutibility. (author) [pt

  18. Isolation of thermally stable cellulose nanocrystals by phosphoric acid hydrolysis.

    Science.gov (United States)

    Camarero Espinosa, Sandra; Kuhnt, Tobias; Foster, E Johan; Weder, Christoph

    2013-04-08

    On account of their intriguing mechanical properties, low cost, and renewable nature, high-aspect-ratio cellulose nanocrystals (CNCs) are an attractive component for many nanomaterials. Due to hydrogen bonding between their surface hydroxyl groups, unmodified CNCs (H-CNCs) aggregate easily and are often difficult to disperse. It is shown here that on account of ionic repulsion between charged surface groups, slightly phosphorylated CNCs (P-CNCs, average dimensions 31 ± 14 × 316 ± 127 nm, surface charge density = 10.8 ± 2.7 mmol/kg cellulose), prepared by controlled hydrolysis of cotton with phosphoric acid, are readily dispersible and form stable dispersions in polar solvents such as water, dimethyl sulfoxide, and dimethylformamide. Thermogravimetric analyses reveal that these P-CNCs exhibit a much higher thermal stability than partially sulfated CNCs (S-CNCs), which are frequently employed, but suffer from limited thermal stability. Nanocomposites of an ethylene oxide-epichlorohydrin copolymer and H-CNCs, S-CNCs, and P-CNCs were prepared, and their mechanical properties were studied by dynamic mechanical thermal analysis. The results show that P-CNCs offer a reinforcing capability that is comparable to that of H-CNCs or S-CNCs.

  19. Pyroelectric properties of phosphoric acid-doped TGS single crystals

    International Nuclear Information System (INIS)

    Saxena, Aparna; Fahim, M; Gupta, Vinay; Sreenivas, K

    2003-01-01

    Pyroelectric properties of phosphoric acid (H 3 PO 4 )-doped triglycine sulfate (TGSP) single crystals grown from solutions containing 0.1-0.5 mol of H 3 PO 4 have been studied. Incorporation of H 3 PO 4 into the crystal lattice is found to induce an internal bias field (E b ) and is observed through the presence of a sustained polarization and pyroelectricity beyond the transition temperature. The internal bias field has been estimated theoretically by fitting the experimentally measured data on temperature dependence of the pyroelectric coefficient (λ), dielectric constant (ε') and polarization (P). A high E b value in the range 9 x 10 3 -15.5 x 10 4 V m -1 is obtained for crystals grown with 0.1-0.5 mol of H 3 PO 4 in the solution, and a specific concentration of 0.2-0.25 mol of H 3 PO 4 in the solution during crystal growth is found to be optimum for a high figure of merit for detectivity, F d = 428 μC m -2 K -1

  20. Pyroelectric properties of phosphoric acid-doped TGS single crystals

    Energy Technology Data Exchange (ETDEWEB)

    Saxena, Aparna; Fahim, M; Gupta, Vinay; Sreenivas, K [Department of Physics and Astrophysics, University of Delhi, Delhi 110007 (India)

    2003-12-21

    Pyroelectric properties of phosphoric acid (H{sub 3}PO{sub 4})-doped triglycine sulfate (TGSP) single crystals grown from solutions containing 0.1-0.5 mol of H{sub 3}PO{sub 4} have been studied. Incorporation of H{sub 3}PO{sub 4} into the crystal lattice is found to induce an internal bias field (E{sub b}) and is observed through the presence of a sustained polarization and pyroelectricity beyond the transition temperature. The internal bias field has been estimated theoretically by fitting the experimentally measured data on temperature dependence of the pyroelectric coefficient ({lambda}), dielectric constant ({epsilon}') and polarization (P). A high E{sub b} value in the range 9 x 10{sup 3}-15.5 x 10{sup 4} V m{sup -1} is obtained for crystals grown with 0.1-0.5 mol of H{sub 3}PO{sub 4} in the solution, and a specific concentration of 0.2-0.25 mol of H{sub 3}PO{sub 4} in the solution during crystal growth is found to be optimum for a high figure of merit for detectivity, F{sub d} = 428 {mu}C m{sup -2} K{sup -1}.

  1. A new planetary structure fabrication process using phosphoric acid

    Science.gov (United States)

    Buchner, Christoph; Pawelke, Roland H.; Schlauf, Thomas; Reissner, Alexander; Makaya, Advenit

    2018-02-01

    Minimising the launch mass is an important aspect of exploration mission planning. In-situ resource utilisation (ISRU) can improve this by reducing the amount of terrestrial materials needed for planetary exploration activities. We report on a recently concluded investigation into the requirements and available technologies for creating hardware on extra-terrestrial bodies, using the limited resources available on site. A trade-off of ISRU technologies for hardware manufacturing was conducted. A new additive manufacturing process suitable for fabricating structures on the Moon or Mars was developed. The process uses planetary regolith as the base material and concentrated phosphoric acid as the liquid binder. Mixing the reagents creates a sticky construction paste that slowly solidifies into a hard, rock-like material. Prior to solidification, the paste is extruded in layers, creating the desired structures in a 3D printing process. We used Martian regolith simulant JSC-Mars-1A, but the process is not selective towards regolith composition. Samples were exposed to thermal cycles and were mechanically characterised. Reduced-scale demonstrator structures were printed to demonstrate structure fabrication using the developed process.

  2. Application of a precipitation method for uranium recovery from abu-zaabal phosphoric acid plant, Egypt

    International Nuclear Information System (INIS)

    El-hazek, N.M.T.; Hussein, E.M.

    1995-01-01

    Current industrial recovery of uranium from 30% phosphoric acid-produced by the dihydrate process-is based on solvent extraction method. Uranium recovery from concentrated phosphoric acid (45-52% p o5 ) produced by evaporation of the 30% acid or directly produced by the hemihydrate process, by solvent extraction is difficult to apply in practice. In addition to possible contamination of the acid by the organic solvents and/or their deterioration. This paper investigates the possibility of applying a precipitation method (Weterings and Janssen, 1985) for uranium recovery from both low (28% P 2 O 5 ) and high (48% P 2 O 5 ) concentration phosphoric acids produced by abu-zaabal phosphoric acid plant (Abuzaabal fertilizers and chemicals Co., Egypt). The 28% acid produced by H 2 SO 4 dihydrate method and the 48% acid produced by evaporation of the 28% acid The applied precipitation method depends on using NH 4 F as a uranium precipitant from both low and high concentration phosphoric acids in presence of acetone as a dispersing agent. All the relevant factors have been studied

  3. Recovery of uranium in the production of concentrated phosphoric acid by a hemihydrate process

    International Nuclear Information System (INIS)

    Nakajima, S.; Miyamoto, M.

    1983-01-01

    Nissan Chemical Industries as manufacturers of phosphoric acid have studied the recovery of uranium, based on a concentrated phosphoric acid production process. The process consists of two stages, a hemihydrate stage with a formation of hemihydrate and a filtration section, followed by a dihydrate stage with hydration and a filtration section. In the hemihydrate stage, phosphate is treated with a mixture of phosphoric acid and sulphuric acid to produce phosphoric acid and hydrous calcium sulphate; the product is recovered in the filtration section and its concentration is 40-50% P 2 O 3 . In the dihydrate stage, the hemihydrate is transformed by re-dissolution and hydration, producing hydrous calcium sulphate, i.e. gypsum. This process therefore comprises two parts, each with different acid concentrations. As the extraction of uranium is easier in the case of a low concentration of phosphoric acid, the process consists of the recovery of uranium starting from the filtrate of the hydration section. The tests have shown that the yield of recovery of uranium was of the order of 80% disregarding the handling losses and no disadvantageous effect has been found in the combination of the process of uranium extraction with the process of concentrated phosphoric acid production. Compared with the classical process where uranium is recovered from acid with 30% P 2 O 5 , the process of producing high-concentration phosphoric acid such as the Nissan process, in which the uranium recovery is effected from acid with 15% P 2 O 5 from the hydration section, presents many advantages [fr

  4. Extraction of americium from acid aqueous solutions by diethyl-2-hexyl-pyro-phosphoric acid

    International Nuclear Information System (INIS)

    Guillaume, Bernard

    1971-02-01

    After having outlined the interesting properties of americium and the difficulties of its recovery, the author reports the study of the mechanism of extraction of americium from acid aqueous solutions by using the diethyl-2hexyl-pyro-phosphoric acid. Several aspects are thus discussed: influence of concentration of H 2 DEHPP, influence of the acidity of the aqueous phase, saturation of extracting agent, influence of the diluting agent, complexing of americium, influence of other cations. In a second part, the author reports the application to the recovery of americium from effluents, and discusses the obtained results

  5. Doping phosphoric acid in polybenzimidazole membranes for high temperature proton exchange membrane fuel cells

    DEFF Research Database (Denmark)

    He, Ronghuan; Li, Qingfeng; Jensen, Jens Oluf

    2007-01-01

    Polybenzimidazole (PBI) membranes were doped in phosphoric acid solutions of different concentrations at room temperature. The doping chemistry was studied using the Scatchard method. The energy distribution of the acid complexation in polymer membranes is heterogeneous, that is, there are two...... different types of sites in PBI for the acid doping. The protonation constants of PBI by phosphoric acid are found to be 12.7 L mol(-1) (K-1) for acid complexing sites with higher affinity, and 0.19 L mol(-1) (K-2) for the sites with lower affinity. The dissociation constants for the complexing acid onto...... these two types of PBI sites are found to be 5.4 X 10(-4) and 3.6 X 10(-2), respectively, that is, about 10 times smaller than that of aqueous phosphoric acid in the first case but 5 times higher in the second. The proton conducting mechanism is also discussed....

  6. Decommissioning of Phosphoric Acid Purification Facility, PT Petrokimia Gresik

    International Nuclear Information System (INIS)

    Zainus Salimin; Nanang TS; Zaid, Ach.; Chotimah; Karyono

    2008-01-01

    Decommissioning of phosporic acid purification facility was the administrative and technical actions taken to allow the removal of some or all of the regulatory control from that facility exploit the phosphoric acid containing uranium. The site location of facility was cleaned up as the clean previous site (green land) for another site project utilization. Decommissioning activities covers the draining of solution or solid powder of remaining process on the equipment, decontamination of site location and equipment wall, dismantling of equipment, decontamination of equipment after dismantling, and decontamination of concrete floor and wall. Uranium contaminated liquid waste and organic solution was treated by bio-oxidation process using bacteria. Remaining solid powder from process (28 drums), contaminated material and equipment after decontamination (60 drums of fire brick, 31 pieces of equipment cut, 2 drums of ashes, 10 drums of active sludge from bio-oxidation process) and concrete splinter of 10 drums of 200 l volume per drum are the radioactive waste that must be sent to Radioactive Waste Technology Centre for its treatment. The non contaminated material and equipment (908 ton) can be reused for reprocessing, some of non contaminated sludge (14.4 m 3 ) and all of non contaminated filtrate water (353 m 3 ) from bio-oxidation process with toxic matters qualification which comply to the its limit values are released on the effluent release drain system of the plant. Clearance level utilizing for filtering contaminated material or equipment was an activity concentration of 1 Bq/g, surface contamination of 1 Bq/cm 2 , effective dose on the 50 cm distance from surface of contaminated material of 0.5 μSv/h (BAPETEN Regulation Letter No. 1459A/P101/PIBN/2008). Limit values for toxic matter are pH 6-9, COD 100 ppm and BOD 50 ppm (Gov. Regulation of East Java No. 45 year of 2002). (author)

  7. External radiation assessment in a wet phosphoric acid production plant

    Energy Technology Data Exchange (ETDEWEB)

    Bolivar, J.P.; Perez-Moreno, J.P. [Dept. Fisica Aplicada, Facultad de Ciencias Experimentales, Universidad de Huelva, 21012 Huelva (Spain); Mas, J.L. [Dept. Fisica Aplicada I, Escuela Universitaria Politecnica, Universidad de Sevilla, 41012 Sevilla (Spain)], E-mail: ppmasb@us.es; Martin, J.E.; San Miguel, E.G. [Dept. Fisica Aplicada, Facultad de Ciencias Experimentales, Universidad de Huelva, 21012 Huelva (Spain); Garcia-Tenorio, R. [Dept. Fisica Aplicada II, Escuela Tecnica Superior de Arquitectura, Universidad de Sevilla, 41012 Sevilla (Spain)

    2009-10-15

    The factories dedicated to the production of phosphoric acid by the so-called wet acid method are usually considered typical NORM industries, because the phosphate rock used as raw material usually contains high concentrations of {sup 238}U-series radionuclides. The magnitude and behaviour of the radionuclides involved in the production process revealed the need to determine its dosimetric impact on workers. This work aims to partially compensate this lack of knowledge through the determination of external effective dose rates at different zones in the process at a typical plant located in the southwest of Spain. To this end, two dosimetric sampling campaigns have been carried out at this phosphoric acid production plant. The first sampling was carried out when phosphate rocks originating in Morocco were processed, and the second one when phosphate rock processed came from the Kola Peninsula (Russia Federation). This differentiation was necessary because the activity concentrations are almost one order of magnitude higher in Moroccan phosphate rock than in Kola phosphate rock. The results obtained have reflected external dose rate enhancements as high as 1.4 {mu}Sv h{sup -1} (i.e., up to thirty times the external exposition due to radionuclides in unperturbed soils) at several points in the facility, particularly where the digested rock (pulp) is filtered. However, the most problematic points are characterised by a small occupation factor. That means that the increment in the annual effective external gamma dose received by the most-exposed worker is clearly below 1 mSv (European Commission limit for the general population) under normal production. Nevertheless, special care in the design and schedule of cleaning and maintaining work in the areas with high doses should be taken in order to avoid any possibility of exceeding the previously mentioned general population limit. In addition, the results of the dosimetric campaign showed no clear correlation between {sup

  8. Progress report on nitric-phosphoric acid oxidation

    International Nuclear Information System (INIS)

    Pierce, R.A.

    1994-01-01

    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

  9. Proton conductivity of phosphoric acid doped polybenzimidazole and its composites with inorganic proton conductors

    DEFF Research Database (Denmark)

    He, Ronghuan; Qingfeng, Li; Gang, Xiao

    2003-01-01

    Phosphoric acid doped polybenzimidazole (PBI) and PBI composite membranes have been prepared in the present work. The PBI composites contain inorganic proton conductors including zirconium phosphate (ZrP), (Zr(HPO4)2·nH2O), phosphotungstic acid (PWA), (H3PW12O40·nH2O) and silicotungstic acid (Si...

  10. Synthesis of new polyphosphonic acids, uranium extracting agents in a phosphoric medium

    International Nuclear Information System (INIS)

    Pensec, T.

    1981-04-01

    Synthesis of organic phosphorus compounds for liquid-liquid extraction of traces of uranium in concentrated phosphoric acid is studied in view of industrial applications. Diphosphonic acids and monoesters and also triphosphonic acids and related compounds are synthetized. Extraction tests show a better efficiency than OPPA [fr

  11. Distribution of lanthanum and neodymium in Di(2-ethlhexyl) phosphoric acid and tributylphosphate

    International Nuclear Information System (INIS)

    Kraikaew, J.; Suparith, N.; Pruantonsai, P.

    1994-01-01

    Lanthanum and neodymium are among the high quantity elements in mixed rare earth from monazite processing. The popular rare earth separation process is liquid-liquid extraction. This research was carried out to study lanthanum and neodymium distribution in two extractants, di(2-ethylhexyl) phosphoric acid and tributylphosphate. The experimental results show that neodymium distributes in both extractants better than lanthanum. The distribution of both elements are higher at low acidity than at high acidity. Quick and rough investigation by calculating the ratio of distribution coefficient of neodymium to lanthanum in each extractant indicated that La-nd separation efficiency of Di(2-ethylhexyl) phosphoric acid is higher than that of tributylphosphate

  12. Effect of phosphoric acid on the morphology and tensile properties of halloysite-polyurethane composites

    Science.gov (United States)

    Gaaz, Tayser Sumer; Luaibi, Hasan Mohammed; Al-Amiery, Ahmed A.; Kadhum, Abdul Amir H.

    2018-06-01

    The high aspect ratio of nanoscale reinforcements enhances the tensile properties of pure polymer matrix. The composites were first made by adding halloysite nanotubes (HNTs) at low weight percentages of 1, 2, and 3 wt% to thermoplastic polyurethane (TPU). Then, HNTs were phosphoric acid-treated before adding to TPU at same weight percentage to create phosphoric acid HNTs-TPU composites. The samples were fabricated using injection moulding. The HNTs-TPU composites were characterized according to the tensile properties including tensile strength, tensile strain and Young's modulus. The loading has shown its highest tensile values at 2 wt% HNTs loading and same findings are shown with the samples that treated with phosphoric acid. The tensile strength increased to reach 24.65 MPa compare with the 17.7 MPa of the neat TPU showing about 26% improvement. For the phosphoric acid-treated composites, the improvement has reached 35% compared to the neat sample. Regarding the tensile stain, the improvement was about 83% at 2 wt% HNTs loading. For Young's modulus, the results obtained in this study have shown that Young's modulus is linearly improved with either the loading content or the phosphoric acid treated achieving its highest values at 3 wt% HNTs of 14.53 MPa and 16.27 MPa for untreated and treated, respectively. FESEM results showed that HNTs were well dispersed in TPU matrix. Thus, HNTs-TPU has improved tensile properties compared with pure TPU due to the addition of nanofiller.

  13. Comparison of different phosphorous adsorption models in acid ...

    African Journals Online (AJOL)

    This study was designed to compare the phosphorous fixation capacity of three soils series named Tyele, Minkonmingon and Mekoto in the south region of Cameroon and to determine the soil properties that are the main predictors of the P activity of those soils. Five adsorption equations viz. Linear, Langmuir, Van Huay, ...

  14. Gel Electrolytes of Covalent Network Polybenzimidazole and Phosphoric Acid by Direct Casting

    DEFF Research Database (Denmark)

    Kirkebæk, Andreas; Aili, David; Henkensmeier, Dirk

    2017-01-01

    for preparing mechanically robust covalent network polybenzimidazole membranes containing up to 95 wt% phosphoric acid. Diamino-terminal pre-polymers of different chain lengths are first prepared, followed by addition of a trifunctional carboxylic acid. The crude solutions are cast and subsequently heat treated...

  15. Dissociation constants of phosphoric acid in dimethylformamide-water mixtures at 298.15 K

    Science.gov (United States)

    Safonova, L. P.; Fadeeva, Yu. A.; Pryakhin, A. A.

    2009-10-01

    The dissociation constants of phosphoric acid (p K 1 and p K 2) in water-dimethylformamide (DMFA) mixtures (0-0.65 mole fractions of DMFA) were determined at 298.15 K by potentiometric titration. The extrapolation of these data to pure DMFA and the comparative calculation method were used to estimate the dissociation constants of the acid in DMFA.

  16. Performance of phosphoric acid activated montmorillonite as buffer materials for radioactive waste repository

    International Nuclear Information System (INIS)

    Wang, Tsing-Hai; Liu, Tsung-Ying; Wu, Ding-Chiang; Li, Ming-Hsu; Chen, Jiann-Ruey; Teng, Shi-Ping

    2010-01-01

    In this study, the performance of phosphoric acid activated montmorillonite (PAmmt) was evaluated by cesium ions adsorption experiments. The PAmmt samples were obtained by activating with 1, 3 and 5 mol L -1 of phosphoric acid, respectively under reflux for 3, 12, and 24 h. Experimental results demonstrated that the treatment of raw K-10 montmorillonite with phosphoric acid increased the materials' affinity for Cs uptake and no significant amount of suspension solids were produced. A relatively insignificant variation in the CEC value was observed. Furthermore, PAmmt also showed high adsorption selectivity toward Cs ions. The improved sorptive properties were mainly related to the increased surface area and the relatively higher surface charge density. Increased specific surface area was the resulted from partial decomposition of lamellar structure of mmt; while the higher surface charge density was caused by the protonation of octahedral Al-OH sites during the acid activation. Generally speaking, stronger acid concentration and longer activation times would produce relatively more decomposed PAmmt particles. However, as the activation exceeds 3 h, the precipitation of Si 4+ would passivate PAmmt against further acid attacks. Based upon our results, acid activation by phosphoric acid could produce PAmmt samples with high sorption capacity and selectivity, and good structural integrity, which are beneficial to be used at radioactive waste repository.

  17. Phosphoric acid doped AB-PBI membranes and its applications in high temperature PEMFC

    DEFF Research Database (Denmark)

    He, Ronghuan; Qingfeng, Li; Bjerrum, Niels

    2005-01-01

    Poly(2,5-benzimidazole) (ab-PBI) was prepared from 3,4-diaminobenzoic acid via a polymerisation reaction. The obtained polymer exhibits excellent thermal stability in a temperature range ….. The membrane of ab-PBI when doped with phosphoric acid at room temperaturepresents high proton conductivity...

  18. Shear bond strength of self-etch adhesives to enamel with additional phosphoric acid etching.

    Science.gov (United States)

    Lührs, Anne-Katrin; Guhr, Silke; Schilke, Reinhard; Borchers, Lothar; Geurtsen, Werner; Günay, Hüsamettin

    2008-01-01

    This study evaluated the shear bond strength of self-etch adhesives to enamel and the effect of additional phosphoric acid etching. Seventy sound human molars were randomly divided into three test groups and one control group. The enamel surfaces of the control group (n=10) were treated with Syntac Classic (SC). Each test group was subdivided into two groups (each n=10). In half of each test group, ground enamel surfaces were coated with the self-etch adhesives AdheSe (ADH), Xeno III (XE) or Futurabond NR (FNR). In the remaining half of each test group, an additional phosphoric acid etching of the enamel surface was performed prior to applying the adhesives. The shear bond strength was measured with a universal testing machine at a crosshead speed of 1 mm/minute after storing the samples in distilled water at 37 degrees C for 24 hours. Fracture modes were determined by SEM examination. For statistical analysis, one-way ANOVA and the two-sided Dunnett Test were used (p>0.05). Additional phosphoric etching significantly increased the shear bond strength of all the examined self-etch adhesives (padhesive fractures. For all the self-etch adhesives, a slight increase in mixed fractures occurred after conditioning with phosphoric acid. An additional phosphoric acid etching of enamel should be considered when using self-etch adhesives. More clinical studies are needed to evaluate the long-term success of the examined adhesives.

  19. Proton conductivity of phosphoric acid doped polybenzimidazole and its composites with inorganic protontic conductors

    DEFF Research Database (Denmark)

    Li, Qingfeng

    2003-01-01

    contain inorganic protonic conductors including zirconium phosphate (ZrP), (Zr(HPO4)2. nH2O); phosphotungstic acid (PWA), (H3PW12O40. nH2O); and silicotungstic acid (SiWA), (H4SiW12O40 . nH2O). The conductivity of phosphoric acid doped PBI and PBI composite membranes was found to be dependent on the acid...

  20. Porous structure and surface chemistry of phosphoric acid activated carbon from corncob

    International Nuclear Information System (INIS)

    Sych, N.V.; Trofymenko, S.I.; Poddubnaya, O.I.; Tsyba, M.M.; Sapsay, V.I.; Klymchuk, D.O.; Puziy, A.M.

    2012-01-01

    Highlights: ► Phosphoric acid activation results in formation of carbons with acidic surface groups. ► Maximum amount of surface groups is introduced at impregnation ratio 1.25. ► Phosphoric acid activated carbons show high capacity to copper. ► Phosphoric acid activated carbons are predominantly microporous. ► Maximum surface area and pore volume achieved at impregnation ratio 1.0. - Abstract: Active carbons have been prepared from corncob using chemical activation with phosphoric acid at 400 °C using varied ratio of impregnation (RI). Porous structure of carbons was characterized by nitrogen adsorption and scanning electron microscopy. Surface chemistry was studied by IR and potentiometric titration method. It has been shown that porosity development was peaked at RI = 1.0 (S BET = 2081 m 2 /g, V tot = 1.1 cm 3 /g), while maximum amount of acid surface groups was observed at RI = 1.25. Acid surface groups of phosphoric acid activated carbons from corncob includes phosphate and strongly acidic carboxylic (pK = 2.0–2.6), weakly acidic carboxylic (pK = 4.7–5.0), enol/lactone (pK = 6.7–7.4; 8.8–9.4) and phenol (pK = 10.1–10.7). Corncob derived carbons showed high adsorption capacity to copper, especially at low pH. Maximum adsorption of methylene blue and iodine was observed for carbon with most developed porosity (RI = 1.0).

  1. Porous structure and surface chemistry of phosphoric acid activated carbon from corncob

    Energy Technology Data Exchange (ETDEWEB)

    Sych, N.V.; Trofymenko, S.I.; Poddubnaya, O.I.; Tsyba, M.M. [Institute for Sorption and Endoecology Problems, National Academy of Sciences of Ukraine, 13 General Naumov St., 03164 Kyiv (Ukraine); Sapsay, V.I.; Klymchuk, D.O. [M.G. Kholodny Institute of Botany, National Academy of Sciences of Ukraine, 2 Tereshchenkivska St., 01601 Kyiv (Ukraine); Puziy, A.M., E-mail: alexander.puziy@ispe.kiev.ua [Institute for Sorption and Endoecology Problems, National Academy of Sciences of Ukraine, 13 General Naumov St., 03164 Kyiv (Ukraine)

    2012-11-15

    Highlights: Black-Right-Pointing-Pointer Phosphoric acid activation results in formation of carbons with acidic surface groups. Black-Right-Pointing-Pointer Maximum amount of surface groups is introduced at impregnation ratio 1.25. Black-Right-Pointing-Pointer Phosphoric acid activated carbons show high capacity to copper. Black-Right-Pointing-Pointer Phosphoric acid activated carbons are predominantly microporous. Black-Right-Pointing-Pointer Maximum surface area and pore volume achieved at impregnation ratio 1.0. - Abstract: Active carbons have been prepared from corncob using chemical activation with phosphoric acid at 400 Degree-Sign C using varied ratio of impregnation (RI). Porous structure of carbons was characterized by nitrogen adsorption and scanning electron microscopy. Surface chemistry was studied by IR and potentiometric titration method. It has been shown that porosity development was peaked at RI = 1.0 (S{sub BET} = 2081 m{sup 2}/g, V{sub tot} = 1.1 cm{sup 3}/g), while maximum amount of acid surface groups was observed at RI = 1.25. Acid surface groups of phosphoric acid activated carbons from corncob includes phosphate and strongly acidic carboxylic (pK = 2.0-2.6), weakly acidic carboxylic (pK = 4.7-5.0), enol/lactone (pK = 6.7-7.4; 8.8-9.4) and phenol (pK = 10.1-10.7). Corncob derived carbons showed high adsorption capacity to copper, especially at low pH. Maximum adsorption of methylene blue and iodine was observed for carbon with most developed porosity (RI = 1.0).

  2. Process engineering challenges of uranium extraction from phosphoric acid on industrial scale

    International Nuclear Information System (INIS)

    Mouriya, Govind; Singh, Dhirendra; Nath, A.K.; Majumdar, D.

    2014-01-01

    Heavy Water Board (HWB) is a constituent unit of the Department of Atomic Energy. One of the diversified activities undertaken by HWB is pursuing exploitation of non-conventional resources for recovery of uranium from wet phosphoric acid being the most prominent one. Amongst the feasible processes for recovery of uranium from phosphoric acid is solvent extraction. Use of in-house solvent produced by HWB, is another key driver. To garner necessary information for developing the industrial scale facilities, the process has been studied in the laboratory scale, mini scale, bench scale at Heavy Water Plant, Talcher. The process was subsequently scaled up to an industrial prototype scale unit and was set up as a Technology Demonstration Plant coupled with a commercial phosphoric acid plant. The plant has successfully processed more than 2 lakh m 3 of wet phosphoric acid and all the parameters including the product, Yellow Cake have been qualified. No adverse effect has been observed in the fertilizer produced. The main characteristics of the process and subsequent process innovations are discussed in this paper. These innovations have been carried out to overcome hurdles faced during commissioning and subsequent operations of the Plant. The innovations include improved pretreatment of the wet phosphoric acid for feeding to the extraction cycle, improved control of the first cycle chemical environment, reducing the strength of the phosphoric acid used for stripping, reducing the number of equipment and machineries, alteration in solvent composition used in the first and second cycle in the solvent extraction units of the plant. (author)

  3. Extraction chromatography of actinides

    International Nuclear Information System (INIS)

    Muller, W.

    1978-01-01

    Extraction chromatography of actinides in the oxidation state from 2 to 6 is reviewed. Data on using neutral (tbp), basic (substituted ammonium salts) and acidic [di-(2-ethylhexyl)-phosphoric acid (D2EHPA)] extracting agents ketones, esters, alcohols and β-diketones in this method are given. Using the example of actinide separation using D2EHPA, discussed are factors influencing the efficiency of their chromatography separation (nature and particle size of the carrier materials, extracting agents amount on the carrier, temperature and elution rate)

  4. Why do proton conducting polybenzimidazole phosphoric acid membranes perform well in high-temperature PEM fuel cells?

    Science.gov (United States)

    Melchior, Jan-Patrick; Majer, Günter; Kreuer, Klaus-Dieter

    2016-12-21

    Transport properties and hydration behavior of phosphoric acid/(benz)imidazole mixtures are investigated by diverse NMR techniques, thermogravimetric analysis (TGA) and conductivity measurements. The monomeric systems can serve as models for phosphoric acid/poly-benzimidazole membranes which are known for their exceptional performance in high temperature PEM fuel cells. 1 H- and 31 P-NMR data show benzimidazole acting as a strong Brønsted base with respect to neat phosphoric acid. Since benzimidazole's nitrogens are fully protonated with a low rate for proton exchange with phosphate species, proton diffusion and conduction processes must take place within the hydrogen bond network of phosphoric acid only. The proton exchange dynamics between phosphate and benzimidazole species pass through the intermediate exchange regime (with respect to NMR line separations) with exchange times being close to typical diffusion times chosen in PFG-NMR diffusion measurements (ms regime). The resulting effects, as described by the Kärger equation, are included into the evaluation of PFG-NMR data for obtaining precise proton diffusion coefficients. The highly reduced proton diffusion coefficient within the phosphoric acid part of the model systems compared to neat phosphoric acid is suggested to be the immediate consequence of proton subtraction from phosphoric acid. This reduces hydrogen bond network frustration (imbalance of the number of proton donors and acceptors) and therefore also the rate of structural proton diffusion, phosphoric acid's acidity and hygroscopicity. Reduced water uptake, shown by TGA, goes along with reduced electroosmotic water drag which is suggested to be the reason for PBI-phosphoric acid membranes performing better in fuel cells than other phosphoric-acid-containing electrolytes with higher protonic conductivity.

  5. Rare earth elements recycling from waste phosphor by dual hydrochloric acid dissolution

    International Nuclear Information System (INIS)

    Liu, Hu; Zhang, Shengen; Pan, Dean; Tian, Jianjun; Yang, Min; Wu, Maolin; Volinsky, Alex A.

    2014-01-01

    Highlights: • The article provides a new method for recycling rare earth (RE) from waste phosphor. • When compared with the traditional methods, leach rate was much higher. • Y–Eu concentrate and Tb–Ce concentrate were obtained successively. • It would reduce the burden of later extraction, separation and purification. - Abstract: This paper is a comparative study of recycling rare earth elements from waste phosphor, which focuses on the leaching rate and the technical principle. The traditional and dual dissolution by hydrochloric acid (DHA) methods were compared. The method of dual dissolution by hydrochloric acid has been developed. The Red rare earth phosphor (Y 0.95 Eu 0.05 ) 2 O 3 in waste phosphor is dissolved during the first step of acid leaching, while the Green phosphor (Ce 0.67 Tb 0.33 MgAl 11 O 19 ) and the Blue phosphor (Ba 0.9 Eu 0.1 MgAl 10 O 17 ) mixed with caustic soda are obtained by alkali sintering. The excess caustic soda and NaAlO 2 are removed by washing. The insoluble matter is leached by the hydrochloric acid, followed by solvent extraction and precipitation (the DHA method). In comparison, the total leaching rate of the rare earth elements was 94.6% by DHA, which is much higher than 42.08% achieved by the traditional method. The leaching rate of Y, Eu, Ce and Tb reached 94.6%, 99.05%, 71.45%, and 76.22%, respectively. DHA can decrease the consumption of chemicals and energy. The suggested DHA method is feasible for industrial applications

  6. Rare earth elements recycling from waste phosphor by dual hydrochloric acid dissolution

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Hu [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Zhang, Shengen, E-mail: zhangshengen@mater.ustb.edu.cn [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Pan, Dean; Tian, Jianjun; Yang, Min; Wu, Maolin [School of Materials Science and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Volinsky, Alex A. [Department of Mechanical Engineering, University of South Florida, Tampa, FL 33620 (United States)

    2014-05-01

    Highlights: • The article provides a new method for recycling rare earth (RE) from waste phosphor. • When compared with the traditional methods, leach rate was much higher. • Y–Eu concentrate and Tb–Ce concentrate were obtained successively. • It would reduce the burden of later extraction, separation and purification. - Abstract: This paper is a comparative study of recycling rare earth elements from waste phosphor, which focuses on the leaching rate and the technical principle. The traditional and dual dissolution by hydrochloric acid (DHA) methods were compared. The method of dual dissolution by hydrochloric acid has been developed. The Red rare earth phosphor (Y{sub 0.95}Eu{sub 0.05}){sub 2}O{sub 3} in waste phosphor is dissolved during the first step of acid leaching, while the Green phosphor (Ce{sub 0.67}Tb{sub 0.33}MgAl{sub 11}O{sub 19}) and the Blue phosphor (Ba{sub 0.9}Eu{sub 0.1}MgAl{sub 10}O{sub 17}) mixed with caustic soda are obtained by alkali sintering. The excess caustic soda and NaAlO{sub 2} are removed by washing. The insoluble matter is leached by the hydrochloric acid, followed by solvent extraction and precipitation (the DHA method). In comparison, the total leaching rate of the rare earth elements was 94.6% by DHA, which is much higher than 42.08% achieved by the traditional method. The leaching rate of Y, Eu, Ce and Tb reached 94.6%, 99.05%, 71.45%, and 76.22%, respectively. DHA can decrease the consumption of chemicals and energy. The suggested DHA method is feasible for industrial applications.

  7. Preliminary study on preparation of BCNO phosphor particles using citric acid as carbon source

    Energy Technology Data Exchange (ETDEWEB)

    Nuryadin, Bebeh W.; Pratiwi, Tripuspita; Faryuni, Irfana D.; Iskandar, Ferry, E-mail: ferry@fi.itb.ac.id; Abdullah, Mikrajuddin; Khairurrijal [Department of Physics, Faculty of Mathematics and Natural Sciences, Institut Teknologi Bandung, Ganesha 10 Bandung, Indonesia 40132 (Indonesia); Ogi, Takashi; Okuyama, Kikuo [Department of Chemical Engineering, Graduate School of Engineering, Hiroshima University, 1-4-1 Kagamiyama, Higashi Hiroshima, Japan 739-8527 (Japan)

    2015-04-16

    A citric acid was used as a carbon source in the preparation of boron carbon oxy-nitride (BCNO) phosphor particles by a facile process. The preparation process was conducted at relatively low temperature 750 °C and at ambient pressure. The prepared BCNO phosphors showed a high photoluminescence (PL) performance at peak emission wavelength of 470 nm under excitation by a UV light 365 nm. The effects of carbon/boron and nitrogen/boron molar ratios on the PL properties were also investigated. The result showed that the emission spectra with a wavelength peak ranging from 444 nm to 496 nm can be obtained by varying carbon/boron ratios from 0.1 to 0.9. In addition, the observations showed that the BCNO phosphor material has two excitation peaks located at the 365 nm (UV) and 420 nm (blue). Based on these observations, we believe that the citric acid derived BCNO phosphor particles can be a promising inexpensive material for phosphor conversion-based white LED.

  8. Determination of uranium content in phosphoric and sulfuric acids used by the phosphatized fertilizers industry

    International Nuclear Information System (INIS)

    Ramos, M.M.O.

    1984-05-01

    Uranium content in phosphoric and sulfuric acids is determined. The uranium was measured through the fission track registration technique, using Makrofol KG, 10 μg thick, as detector. The so-called 'wet' method was adopted and the acid samples were used directly as irradiation medium. This proceeding showed the advantages of simple sample preparation and avoided the need of changing the acid samples media to nitric medium, as commonly used. The analysis of the sulfuric acid samples showed uranium contents under the detection limit of the technique (4 ppb). The results found for phosphoric acid samples ranged from 31 to 845 ppm, with experimental errors between 7.9 and 9.7%. (Author) [pt

  9. PREPARATION OF METAL OXIDE POWDERS FROM METAL LOADED VERSATIC ACID

    OpenAIRE

    KAKIHATA, Takayuki; USAMI, Kensuke; YAMAMOTO, Hideki; SHIBATA, Junji

    1998-01-01

    A production process for metal oxide powders was developed using a solvent extraction method. Versatic Acid 10 and D2EHPA solutions containing copper, zinc and nickel were used for a precipitation-stripping process, where oxalic acid was added to the solution as a precipitation reagent.Copper, zinc and nickel oxalates were easily formed in an aqueous phase, and 99.9% of precipitation was obtained for each metal during this process. These metal oxalates were easily converted to metal oxides by...

  10. Corrosion rate of construction materials in hot phosphoric acid with the contribution of anodic polarization

    DEFF Research Database (Denmark)

    Kouril, M.; Christensen, Erik; Eriksen, S.

    2011-01-01

    The paper is focused on selection of a proper material for construction elements of water electrolysers, which make use of a 85% phosphoric acid as an electrolyte at temperature of 150 8C and which might be loaded with anodic polarization up to 2.5 V versus a saturated Ag/AgCl electrode (SSCE...

  11. Determination of elemental impurities in phosphoric acid by INAA employing a novel method of phosphate precipitation

    Czech Academy of Sciences Publication Activity Database

    Kameník, Jan; Amsil, H.; Kučera, Jan

    2015-01-01

    Roč. 304, APR (2015), s. 157-162 ISSN 0236-5731 R&D Projects: GA ČR(CZ) GBP108/12/G108; GA MŠk LM2011019 Institutional support: RVO:61389005 Keywords : instrumental neutron activation analysis * phosphoric acid * elemental impurities * isothermal distillation Subject RIV: CB - Analytical Chemistry, Separation Impact factor: 0.983, year: 2015

  12. Determination of elemental impurities in phosphoric acid by INAA employing a novel method of phosphate precipitation

    Czech Academy of Sciences Publication Activity Database

    Kameník, Jan; Amsil, H.; Kučera, Jan

    2014-01-01

    Roč. 2014, AUG (2014), s. 3455 ISSN 1588-2780 R&D Projects: GA ČR(CZ) GBP108/12/G108; GA MŠk(XE) LM2011019 Institutional support: RVO:61389005 Keywords : instrumental neutron activation analysis * phosphoric acid * elemental impurities * isothermal distillation Subject RIV: BG - Nuclear, Atomic and Molecular Physics, Colliders

  13. Survey on aging on electrodes and electrocatalysts in phosphoric acid fuel cells

    Science.gov (United States)

    Stonehart, P.; Hochmuth, J.

    1981-01-01

    The processes which contribute to the decay in performance of electrodes used in phosphoric acid fuel cell systems are discussed. Loss of catalytic surface area, corrosion of the carbon support, electrode structure degradation, electrolyte degradation, and impurities in the reactant streams are identified as the major areas for concern.

  14. Measurement of the oxidation-extraction of uranium from wet-process phosphoric acid

    International Nuclear Information System (INIS)

    Lawes, B.C.

    1985-01-01

    The present invention relates to processes for the recovery of uranium from wet-process phosphoric acid and more particularly to the oxidation-extraction steps in the DEPA-TOPO process for such recovery. A more efficient use of oxidant is obtained by monitoring the redox potential during the extraction step

  15. Catalyst evaluation for oxygen reduction reaction in concentrated phosphoric acid at elevated temperatures

    DEFF Research Database (Denmark)

    Hu, Yang; Jiang, Yiliang; Jensen, Jens Oluf

    2018-01-01

    Phosphoric acid is the common electrolyte for high-temperature polymer electrolyte fuel cells (HT-PEMFCs) that have advantages such as enhanced CO tolerance and simplified heat and water management. The currently used rotating disk electrode technique is limited to tests in dilute solutions at lo...

  16. Interfacial characteristics of an epoxy composite reinforced with phosphoric acid-functionalized Kevlar fibers

    Science.gov (United States)

    Li, J.; Xia, Y. C.

    2010-07-01

    A Kevlar fiber was functionalized with the phosphoric acid (PA) of different concentrations. The surface characteristics of the fiber were examined by using the X-ray photoelectron spectroscopy. It was found that the PA functionalization considerably increased the bond strength between the Kevlar fiber and an epoxy matrix.

  17. Influence of pH-control in phosphoric acid treatment of zinc oxide

    Energy Technology Data Exchange (ETDEWEB)

    Onoda, H., E-mail: onoda@kpu.ac.jp [Department of Informatics and Environmental Sciences, Kyoto Prefectural University (Japan); Chemel, M. [Ecole de Biologie Industrielle, CERGY Cedex (France)

    2017-04-15

    Zinc oxide is often used as a white pigment for cosmetics; however, it shows photocatalytic activity that causes decomposition of sebum on the skin when exposed to the ultraviolet radiation in sunlight. In this work, zinc oxide was reacted with phosphoric acid at various pH values to synthesize a novel white pigment for cosmetics. The chemical composition, powder properties, photocatalytic activities, colors, and smoothness of these pigments were studied. The obtained materials exhibited X-ray diffraction peaks relating to zinc oxide and phosphate after phosphoric acid treatment. The ratio of zinc phosphate to zinc oxide was estimated from inductively coupled plasma - atomic emission spectroscopy results. Samples treated at pH 4-7 yielded small particles with sub-micrometer sizes. The photocatalytic activity of zinc oxide became lower after phosphoric acid treatment. Samples treated at pH 4-7 showed the same reflectance as zinc oxide in both the ultraviolet and visible ranges. Adjustment of the pH was found to be important in the phosphoric acid treatment of zinc oxide. (author)

  18. A contribution to the study of mass transfer: uranium extraction from phosphoric acid

    International Nuclear Information System (INIS)

    Maher, A.

    1985-12-01

    Liquid-liquid extraction of uranium (VI) contained in phosphoric acid is examined. Synergism and thermodynamical equilibria are studied. Influence of drop size, extractant concentration and temperature on reaction kinetics are determined. The experimental study concerns extraction by HDEHP, TOPO and the mixture of both. Reaction mechanisms are interpreted [fr

  19. Activated carbon from peach stones using phosphoric acid activation at medium temperatures.

    Science.gov (United States)

    Kim, Dong-Su

    2004-01-01

    In the present study, the activation features of phosphoric acid have been investigated using waste peach stones as the raw material in the production of granular activated carbon. Thermogravimetry/differential thermal analysis was conducted to characterize the thermal behavior of peach stone and titration method was used to evaluate the adsorption capacity of the produced activated carbon. It was observed that the iodine value of the activated carbon increased with activation temperature. However, temperatures higher than 500 degrees C caused a thermal destruction, which resulted in the decrease of the adsorption capacity. Activation longer than 1.5 h at 500 degrees C resulted in thermal degradation of the porous structure of the activated carbon. The adsorption capacity was enhanced with increasing of amounts of phosphoric acid, however, excessive phosphoric acid caused a decrease in the iodine value. In addition, it was found that the carbon yields generally decreased with activation temperature and activation time. Scanning electron microscopy analysis was conducted to observe the changes in the poros structure of the activated carbon produced in different temperatures. Activation of carbon by phosphoric acid was found to be superior to that by CaCl2 and gas activation. The activated carbon produced from peach stone was applied as an adsorbent in the treatment of synthesized wastewater containing cadmium ion and its adsorption capacity was found to be as good as that of the commercial one.

  20. Brewer’s Spent Grain Valorization Using Phosphoric Acid Pretreatment for Second Generation Bioethanol Production

    DEFF Research Database (Denmark)

    Romero, I.; Ruiz, E.; Cara, C.

    the effect of phosphoric acid concentration (2-6% w/v) and pretreatment temperature (140-180ºC). The influence of these factors on the hemicellulosic sugar solubilisation and the subsequent enzymatic hydrolysis was evaluated. Optimal pretreatment conditions were determined by maximizing both...... hemicellulosic sugar recovery in liquids and enzymatic hydrolysis yield....

  1. Phosphoric acids as amplifiers of molecular chirality in liquid crystalline media

    NARCIS (Netherlands)

    Eelkema, R; Feringa, BL

    2006-01-01

    A new system for the double amplification of the molecular chirality of simple chiral amines in achiral liquid crystalline media is described. It involves a conformationally flexible phosphoric acid based receptor that by binding to chiral amines induces chirality in the liquid crystalline matrix.

  2. Phosphoric acid doped polysulfone membranes with aminopyridine pendant groups and imidazole cross-links

    DEFF Research Database (Denmark)

    Hink, Steffen; Elsøe, Katrine; Cleemann, Lars Nilausen

    2015-01-01

    Udel polysulfone based membranes with 4-aminopyridine pendant groups and cross-linking imidazole units are synthesized in a simple two step reaction. The ratio of 4-aminopyridine and imidazole is varied and the materials are extensively characterized. The average phosphoric acid uptake (in 85 wt%...

  3. Phosphoric acid doped imidazolium polysulfone membranes for high temperature proton exchange membrane fuel cells

    DEFF Research Database (Denmark)

    Yang, Jingshuai; Li, Qingfeng; Jensen, Jens Oluf

    2012-01-01

    A novel acid–base polymer membrane is prepared by doping of imidazolium polysulfone with phosphoric acid for high temperature proton exchange membrane fuel cells. Polysulfone is first chloromethylated, followed by functionalization of the chloromethylated polysulfone with alkyl imidazoles i.e. me...

  4. Manual of phosphoric acid fuel cell power plant cost model and computer program

    Science.gov (United States)

    Lu, C. Y.; Alkasab, K. A.

    1984-01-01

    Cost analysis of phosphoric acid fuel cell power plant includes two parts: a method for estimation of system capital costs, and an economic analysis which determines the levelized annual cost of operating the system used in the capital cost estimation. A FORTRAN computer has been developed for this cost analysis.

  5. Experiences from Swedish demonstration projects with phosphoric acid fuel cells; Erfarenheter fraan svenska demonstrationsprojekt med fosforsyrabraensleceller

    Energy Technology Data Exchange (ETDEWEB)

    Carlsson, Per [Sycon Energikonsult AB, Stockholm (Sweden); Sarkoezi, Laszlo [Vattenfall Utveckling AB, Stockholm (Sweden)

    1999-10-01

    In Sweden, there are today two phosphoric acid fuel cells installed, one PC25A which have been in operation in more than 4 years, and one PC25C which have been in operation for two years. The aim with this project has been two compare operation characteristics, performance, and operation experiences for these two models.

  6. Proton conductance at elevated temperature:Formulation and investigation of poly(4-styrenesulfonic acid / 4-aminobenzylamine / phosphoric acid membranes

    Directory of Open Access Journals (Sweden)

    Jalal eJalili

    2014-07-01

    Full Text Available 4-aminobenzylamine and phosphoric acid were blended in various proportions with poly (4-styrenesulfonic acid to form a new group of membranes exhibiting proton conductance under water-free conditions. The 4-aminobenzylamine molecule, possessing an aniline-like and benzylamine-like functional group, can interact both with the phosphoric acid and the poly(4-styrenesulfonic acid via nucleophilic interaction, thereby allowing proton jumping in the structure. Physico-chemical and thermal characteristics of the prepared solid membranes were investigated by IR spectroscopy and thermo-gravimetric analysis, respectively. Electrochemical impedance spectroscopy was employed to investigate their proton-conductance properties. Transparent composite membranes were prepared. However, the membranes are opaque for relatively high content of phosphoric acid. These membranes are thermally stable up to 300°C. The proton conductivity increases with temperature and also with content of phosphoric acid. Values as high as 1.8×10–3 S cm–1 were measured at 190°C in fully anhydrous condition.

  7. On the reaction of iron oxides and oxyhydroxides with tannic and phosphoric acid and their mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Beltran, J. J., E-mail: jjbj08@yahoo.com; Novegil, F. J.; Garcia, K. E.; Barrero, C. A. [Universidad de Antioquia, Sede de Investigacion Universitaria, Grupo de Estado Solido, Instituto de Fisica (Colombia)

    2010-01-15

    The actions of tannic acid, phosphoric acid and their mixture on lepidocrocite, goethite, superparamagnetic goethite, akaganeite, magnetite, hematite and maghemite for 1 day and 1 month were explored. It was found that these acids form iron tannates and phosphates. Lepidocrocite and magnetite were the iron phases more easily transformed with the mixture of the acids after 1 month of reaction, whereas hematite was the most resistant phase. In the case of goethite, our results suggest that in order to understand properly the action of these acids, we have to take into account its stoichiometry, surface area and degree of crystallinity.

  8. Extraction of uranium from wet process phosphoric acid in centrifugal and mixer-settler batteries

    International Nuclear Information System (INIS)

    Poczynajlo, A.; Giers, M.

    1986-01-01

    Five stage countercurrent batteries were comparatively applied for the extraction of uranium from wet phosphoric acid (Chemical Works, Police) in semitechnical scale. As an extractant phase the 0.16 M equimolar solution of mono- and dinonylphenyolphosphoric acids in kerosene was used. The optimum hydrodynamic and extraction conditions for the batteries were found. Process efficiencies of the apparatus were also determined. 5 refs., 5 figs., 2 tabs. (author)

  9. The use of Syrian bentonite to remove organics and other ions from commercial Syrian phosphoric acid

    International Nuclear Information System (INIS)

    Khorfan, S.; Abdulbaki, M.; Zein, A.

    2006-01-01

    Using of activated carbon to remove organic matter from phosphoric acid in uranium and P 2 O 5 extraction units has high cost. A new study was conducted to establish a new material instead of activated carbon. Experiments were carried out on removing organic matter by adsorption on Syrian bentonite. The experiments of the removal of humic acid by Syrian bentonite gave good results and showed that the chemical and thermal activation of bentonite increased the adsorption efficiency. (Authors)

  10. The use of Syrian bentonite to remove organics and other ions from commercial Syrian phosphoric acid

    International Nuclear Information System (INIS)

    Khorfan, S.; Abdulbaki, M.; Zein, A.

    2005-03-01

    Using of activated carbon to remove organic matter from phosphoric acid in uranium and P 2 O 5 extraction units has high cost. A new study was conducted to establish a new material instead of activated carbon. Experiments were carried out on removing organic matter by adsorption on Syrian bentonite. The experiments of the removal of humic acid by Syrian bentonite gave good results and showed that the chemical and thermal activation of bentonite increased the adsorption efficiency. (Authors)

  11. On the fractionation of natural radioactivity in the production of phosphoric acid by the wet acid method

    International Nuclear Information System (INIS)

    Bolivar, J.P.; Garcia-Tenorio, R.; Garcia-Leon, M.

    1996-01-01

    The fractionation of different natural radionuclides (U-isotopes, 226 Ra and 210 Po) in the process used for the production of phosphoric acid in some factories located in the south-west of Spain is analyzed. As a consequence, different ways of natural radionuclide liberation to the environment can be evaluated due to these industrial activities. (author). 9 refs., 2 figs., 3 tabs

  12. Carbon-13 kinetic isotope effects in the decarbonylation of lactic acid of natural isotopic composition in phosphoric acid medium

    International Nuclear Information System (INIS)

    Zielinski, M.; Czarnota, G.; Papiernik-Zielinska, H.; Kasprzyk, G.; Gumolka, L.; Staedter, W.

    1993-01-01

    The 13 C kinetic isotope effect fractionation in the decarbonylation of lactic acid (LA) of natural isotopic composition by concentrated phosphoric acids (PA) and by 85% H 3 PO 4 has been studied in the temperature interval of 60-150 deg C. The values of the 13 C (1) isotope effects in the decarbonylation of lactic acid in 100% H 3 PO 4 , in pyrophosphoric acid and in more concentrated phosphoric acids are intermediate between the values calculated assuming that the C (1)- OH bond is broken in the rate-controlling step of dehydration and those calculated for rupture of the carbon-carbon bond in the transition state. In the temperature interval of 90-130 deg C the experimental 13 C fractionation factors determined in concentrated PA approach quite closely the 13 C fractionation corresponding to C (2)- C (1) bond scission. The 13 C (1) kinetic isotope effects in the decarbonylation of LA in 85% orthophosphoric acid in the temperature range of 110-150 deg C coincide with the 13 C isotope effects calculated assuming that the frequency corresponding to the C (1) -OH vibration is lost in the transition state of decarbonylation. A change of the mechanism of decarbonylation of LA in going from concentrated PA medium to 85% H 3 PO 4 has been suggested. A possible secondary 18 O and a primary 18 O kinetic isotope effect in decarbonylation of lactic acid in phosphoric acids media have been discussed, too. (author) 21 refs.; 3 tabs

  13. Corrosion rate of construction materials in hot phosphoric acid with the contribution of anodic polarization

    Energy Technology Data Exchange (ETDEWEB)

    Kouril, M. [Institute of Chemical Technology, Technicka 5, 166 28 Prague (Czech Republic); Christensen, E. [Technical University of Denmark, Kemitorvet, 2800 Kgs. Lyngby (Denmark); Eriksen, S.; Gillesberg, B. [Tantaline A/S, Nordborgvej 81, 6430 Nordborg (Denmark)

    2012-04-15

    The paper is focused on selection of a proper material for construction elements of water electrolysers, which make use of a 85% phosphoric acid as an electrolyte at temperature of 150 C and which might be loaded with anodic polarization up to 2.5 V versus a saturated Ag/AgCl electrode (SSCE). Several grades of stainless steels were tested as well as tantalum, niobium, titanium, nickel alloys and silicon carbide. The corrosion rate was evaluated by means of mass loss at free corrosion potential as well as under various levels of polarization. The only corrosion resistant material in 85% phosphoric acid at 150 C and at polarization of 2.5 V/SSCE is tantalum. In that case, even a gentle cathodic polarization is harmful in such an acidic environment. Hydrogen reduction leads to tantalum hydride formation, to loss of mechanical properties and to complete disintegration of the metal. Contrary to tantalum, titanium is free of any corrosion resistance in hot phosphoric acid. Its corrosion rate ranges from tens of millimetres to metres per year depending on temperature of the acid. Alloy bonded tantalum coating was recognized as an effective corrosion protection for both titanium and stainless steel. Its serviceability might be limited by slow dissolution of tantalum that is in order of units of mm/year. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  14. Inorganic-Organic hybrid materials for uranium extraction from phosphoric acid

    International Nuclear Information System (INIS)

    El-Mourabit, Sabah

    2013-01-01

    Phosphate rocks are industrially processed in large quantities to produce phosphoric acid and fertilisers. These rocks contain significant concentration of uranium (50 to 300 ppm) which could be interesting for nuclear industry. This work deals with the valorisation of uranium as a by-product from fertiliser industry. The aim of this study is to develop a hybrid material, constituted of an inorganic solid support grafted with an extractant (complexing molecule), which can extract selectively uranium from phosphoric acid medium. The first step of our approach was to identify an inorganic support which is stable under these particular conditions (strong acidity and complexing medium). The chemical and mechanical stability of different meso-porous materials, such as silica, glass and carbon was studied. In a second phase, we focused on the identification and the optimisation of complexing molecules, specific of uranium in phosphoric acid. These ligands were then grafted on the most stable solids. Finally, the efficiency of these hybrid systems was evaluated through different tests of extraction, selectivity and de-extraction. (author) [fr

  15. Solid phase extraction of uranium from phosphoric acid. Kinetic and thermodynamic study

    Energy Technology Data Exchange (ETDEWEB)

    Abdel-Magied, Ahmed Fawzy [Nuclear Materials Authority, Cairo (Egypt); Stockholm Univ. (Sweden). Dept. of Organic Chemistry

    2017-07-01

    There is a high interest to develop suitable solid phase extractants for uranium separation from aqueous solutions in order to reduce cost and enhance the efficiency. This paper describes solid phase extraction of uranium(VI) from aqueous phosphoric acid solution using MCM-41 based D2HEPA-TOPO organophosphorous extractants. The mixture of D2HEPA (di-2-ethyl-hexylphosphoric acid) and TOPO (tri-n-octylphosphine oxide) was impregnated into the pores of MCM-41 and the synthesized sorbent was fully characterized. The influences of different factors such as synergistic mixture ratio, phosphoric acid concentration, mixing time and temperature were investigated. The results showed that 90% of uranium(VI) extraction can be achieved within 5 min, using D2HEPA-TOPO rate at MCM-41 (mass ratio 2:1 w/w) from 1 M phosphoric acid containing 64 ppm of uranium at room temperature. High adsorption capacity of uranium(VI) have been achieved at the mentioned conditions. The rate constant for the chemical adsorption of uranium(VI) was 0.988 g mg{sup -1} min{sup -1} calculated by the pseudo-second order rate equation. The obtained thermodynamics parameters showed that uranium(VI) adsorption from H{sub 3}PO{sub 4} is an exothermic and spontaneous process.

  16. Effect of acetic acid on wet patterning of copper/molybdenum thin films in phosphoric acid solution

    International Nuclear Information System (INIS)

    Seo, Bo.-Hyun; Lee, Sang-Hyuk; Park, In-Sun; Seo, Jong Hyun; Choe, HeeHwan; Jeon, Jae-Hong; Hong, Munpyo; Lee, Yong Uk; Winkler, Joerg

    2011-01-01

    Copper metallization is a key issue for high performance thin film transistor (TFT) technology. A phosphoric acid based copper etchant is a potentially attractive alternative to the conventional hydrogen peroxide based etchant due to its longer-life expectancy time and higher stability in use. In this paper, it is shown that amount of the acetic acid in the phosphoric based copper etchant plays an important role in controlling the galvanic reaction between the copper and the molybdenum. As the concentration of acetic acid in the phosphoric mixture solution increased from 0 M to 0.4 M, the measured galvanic current density dropped from 32 mA/cm 2 to 26 mA/cm 2 , indicating that the acetic acid induces the lower galvanic reaction between the copper and the molybdenum in the solution. From the XPS analysis, with the addition of the acetic acid, the thickness of the protective MoO 2 passive film covering the molybdenum surface grew and the dissolution rate of the molybdenum thin film decreased. However, the dissolution rate of the copper thin film increased as the concentration of acetic acid in the mixture solution increased.

  17. Effect of acetic acid on wet patterning of copper/molybdenum thin films in phosphoric acid solution

    Energy Technology Data Exchange (ETDEWEB)

    Seo, Bo.-Hyun; Lee, Sang-Hyuk; Park, In-Sun [Department of Materials Engineering, Korea Aerospace University, Hwajeon, Goyang, Gyonggi-do 412-791 (Korea, Republic of); Seo, Jong Hyun, E-mail: jhseo@kau.ac.kr [Department of Materials Engineering, Korea Aerospace University, Hwajeon, Goyang, Gyonggi-do 412-791 (Korea, Republic of); Choe, HeeHwan; Jeon, Jae-Hong [School of Electronics, Telecommunications and Computer Engineering, Korea Aerospace University, Hwajeon, Goyang, Gyonggi-do 412-791 (Korea, Republic of); Hong, Munpyo [Display and Semiconductor Physics, Korea University (Korea, Republic of); Lee, Yong Uk [PETEC (The Printable Electronics Technology Centre) (United Kingdom); Winkler, Joerg [PLANSEE Metal GmbH, Metallwerk-Plansee-Str. 71A-6600, Reutte (Austria)

    2011-08-01

    Copper metallization is a key issue for high performance thin film transistor (TFT) technology. A phosphoric acid based copper etchant is a potentially attractive alternative to the conventional hydrogen peroxide based etchant due to its longer-life expectancy time and higher stability in use. In this paper, it is shown that amount of the acetic acid in the phosphoric based copper etchant plays an important role in controlling the galvanic reaction between the copper and the molybdenum. As the concentration of acetic acid in the phosphoric mixture solution increased from 0 M to 0.4 M, the measured galvanic current density dropped from 32 mA/cm{sup 2} to 26 mA/cm{sup 2}, indicating that the acetic acid induces the lower galvanic reaction between the copper and the molybdenum in the solution. From the XPS analysis, with the addition of the acetic acid, the thickness of the protective MoO{sub 2} passive film covering the molybdenum surface grew and the dissolution rate of the molybdenum thin film decreased. However, the dissolution rate of the copper thin film increased as the concentration of acetic acid in the mixture solution increased.

  18. Analytical applications of condensed phosphoric acid-I Determination of ferrous and total iron in iron ores after decomposition with condensed phosphoric acid.

    Science.gov (United States)

    Mizoguchi, T; Ishii, H

    1978-06-01

    A simple method is described for the determination of ferrous and total iron in iron ores. Iron ores are dissolved by condensed phosphoric acid (CPA) very rapidly without any tedious and time-consuming manipulations such as elimination of silica and filtration. Under the proposed conditions (amount of sample 100 mg, amount of CPA added 10 g, heating temperature 290 degrees , heating time 30 min), magnetite, limonite and hematite are completely dissolved. The iron content can be determined in the presence of condensed phosphoric acid by titration with dichromate solution, if a slight modification is made. The total iron in iron ores, determined by the present method, is in agreement with that found by the JIS method. The ferrous iron in iron ores can be determined by dissolving the samples with CPA in a nitrogen atmosphere and titrating with dichromate solution. Chelatometric titration of iron after solvent extraction with MIBK from solutions prepared by use of CPA is found to be accurate for samples such as pyrite cinder. The ability of CPA to dissolve various materials has been investigated.

  19. Method for the recovery of uranium from phosphoric acid, originating from the wet-process of uraniferous phosphate ores

    International Nuclear Information System (INIS)

    Pyrih, R.Z.; Rickard, R.S.; Carrington, O.F.

    1978-01-01

    Improvement in the process for recoverying uranium from wet-process phosphoric acid solution derived from the acidulation of uraniferous phosphate ores by the use of two ion exchange circuits is described. (Auth.)

  20. Structural and morphological changes in supramolecular-structured polymer electrolyte membrane fuel cell on addition of phosphoric acid

    Science.gov (United States)

    Hendrana, S.; Pryliana, R. F.; Natanael, C. L.; Rahayu, I.

    2018-03-01

    Phosphoric acid is one agents used in membrane fuel cell to modify ionic conductivity. Therefore, its distribution in membrane is a key parameter to gain expected conductivity. Efforts have been made to distribute phosphoric acid in a supramolecular-structured membrane prepared with a matrix. To achieve even distribution across bulk of the membrane, the inclusion of the polyacid is carried out under pressurized chamber. Image of scanning electron microscopy (SEM) shows better phosphoric acid distribution for one prepared in pressurized state. It also leads in better performing in ionic conductivity. Moreover, data from differential scanning calorimetry (DSC) indicate that the addition of phosphoric acid is prominent in the change of membrane structure, while morphological changes are captured in SEM images.

  1. Phosphoric acid as a matrix additive for MALDI MS analysis of phosphopeptides and phosphoproteins

    DEFF Research Database (Denmark)

    Kjellström, Sven; Jensen, Ole Nørregaard

    2004-01-01

    Phosphopeptides are often detected with low efficiency by MALDI MS analysis of peptide mixtures. In an effort to improve the phosphopeptide ion response in MALDI MS, we investigated the effects of adding low concentrations of organic and inorganic acids during peptide sample preparation in 2,5-di...... acid to 2,5-DHB were also observed in LC-MALDI-MS analysis of tryptic phosphopeptides of B. subtilis PrkC phosphoprotein. Finally, the mass resolution of MALDI mass spectra of intact proteins was significantly improved by using phosphoric acid in 2,5-DHB matrix....

  2. Effect of Phosphoric Acid Pre-etching on Fatigue Limits of Self-etching Adhesives.

    Science.gov (United States)

    Takamizawa, T; Barkmeier, W W; Tsujimoto, A; Scheidel, D D; Erickson, R L; Latta, M A; Miyazaki, M

    2015-01-01

    The purpose of this study was to use shear bond strength (SBS) and shear fatigue limit (SFL) testing to determine the effect of phosphoric acid pre-etching of enamel and dentin prior to application of self-etch adhesives for bonding resin composite to these substrates. Three self-etch adhesives--1) G- ænial Bond (GC Corporation, Tokyo, Japan); 2) OptiBond XTR (Kerr Corp, Orange, CA, USA); and 3) Scotchbond Universal (3M ESPE Dental Products, St Paul, MN, USA)--were used to bond Z100 Restorative resin composite to enamel and dentin surfaces. A stainless-steel metal ring with an inner diameter of 2.4 mm was used to bond the resin composite to flat-ground (4000 grit) tooth surfaces for determination of both SBS and SFL. Fifteen specimens each were used to determine initial SBS to human enamel/dentin, with and without pre-etching with a 35% phosphoric acid (Ultra-Etch, Ultradent Products Inc, South Jordan, UT, USA) for 15 seconds prior to the application of the adhesives. A staircase method of fatigue testing (25 specimens for each test) was then used to determine the SFL of resin composite bonded to enamel/dentin using a frequency of 10 Hz for 50,000 cycles or until failure occurred. A two-way analysis of variance and Tukey post hoc test were used for analysis of SBS data, and a modified t-test with Bonferroni correction was used for the SFL data. Scanning electron microscopy was used to examine the area of the bonded restorative/tooth interface. For all three adhesive systems, phosphoric acid pre-etching of enamel demonstrated significantly higher (padhesives clearly demonstrated different tendencies between enamel and dentin. The effect of using phosphoric acid, prior to the application of the self-etching adhesives, on SBS and SFL was dependent on the adhesive material and tooth substrate and should be carefully considered in clinical situations.

  3. Evaluation of two processes for the production of phosphoric acid in pilot scale

    International Nuclear Information System (INIS)

    Santos Benedetto, J. dos.

    1984-01-01

    Two processes for the production of phosphoric acid, based on dihydrate route and hemihydrate route, have been evaluated. The processes were tested in a pilot plant using the concentrate obtained from phosphorus-uraniferous mineral from Itataia mines (CE, Brazil). Results were evaluated from the data obtained from phosphorus and uranium solubilizations. Also presented, although in a summarised way, are the description of the construction of the pilot plants and the analytical methods for the follow-up of processes. (Author) [pt

  4. Separation of transuranium elements from high-level waste by extraction with diisodecyl phosphoric acid

    International Nuclear Information System (INIS)

    Morita, Y.; Kubota, M.; Tani, S.

    1991-01-01

    Separation of transuranic elements (TRU) by extraction with diisodecyl phosphoric acid (DIDPA) has been studied to develop a partitioning process for high-level waste (HLW). In the present study, experiments of counter-current continuous extraction and back-extraction using a miniature mixer-settler were carried out to find the optimum process condition for the separation of Np initially in the pentavalent state and to examine the extraction behaviors of fission and corrosion products. (J.P.N.)

  5. Determination of uranium in urine samples for workers in the phosphoric acid purification using fluorimetry technique

    International Nuclear Information System (INIS)

    Kharita, M. H.; Sakhita, Kh.; Aldalal, Z.

    2003-10-01

    There is probability of exposure to uranium for workers in the phosphoric acid purification (internal exposure) by inhalation, and the deposition of this uranium in organs and tissues, and the consequence excreation out of the body by perspiration or urine. This study focuses on the determination of uranium in urine samples of workers. All results seem to be under the detection limit of the method, therefore no routine monitoring is required. (author)

  6. Complexity in Acid–Base Titrations: Multimer Formation Between Phosphoric Acids and Imines

    Science.gov (United States)

    Malm, Christian; Kim, Heejae; Wagner, Manfred

    2017-01-01

    Abstract Solutions of Brønsted acids with bases in aprotic solvents are not only common model systems to study the fundamentals of proton transfer pathways but are also highly relevant to Brønsted acid catalysis. Despite their importance the light nature of the proton makes characterization of acid–base aggregates challenging. Here, we track such acid–base interactions over a broad range of relative compositions between diphenyl phosphoric acid and the base quinaldine in dichloromethane, by using a combination of dielectric relaxation and NMR spectroscopy. In contrast to what one would expect for an acid–base titration, we find strong deviations from quantitative proton transfer from the acid to the base. Even for an excess of the base, multimers consisting of one base and at least two acid molecules are formed, in addition to the occurrence of proton transfer from the acid to the base and simultaneous formation of ion pairs. For equimolar mixtures such multimers constitute about one third of all intermolecular aggregates. Quantitative analysis of our results shows that the acid‐base association constant is only around six times larger than that for the acid binding to an acid‐base dimer, that is, to an already protonated base. Our findings have implications for the interpretation of previous studies of reactive intermediates in organocatalysis and provide a rationale for previously observed nonlinear effects in phosphoric acid catalysis. PMID:28597513

  7. Optimization of cellulose nanocrystal length and surface charge density through phosphoric acid hydrolysis

    Science.gov (United States)

    Vanderfleet, Oriana M.; Osorio, Daniel A.; Cranston, Emily D.

    2017-12-01

    Cellulose nanocrystals (CNCs) are emerging nanomaterials with a large range of potential applications. CNCs are typically produced through acid hydrolysis with sulfuric acid; however, phosphoric acid has the advantage of generating CNCs with higher thermal stability. This paper presents a design of experiments approach to optimize the hydrolysis of CNCs from cotton with phosphoric acid. Hydrolysis time, temperature and acid concentration were varied across nine experiments and a linear least-squares regression analysis was applied to understand the effects of these parameters on CNC properties. In all but one case, rod-shaped nanoparticles with a high degree of crystallinity and thermal stability were produced. A statistical model was generated to predict CNC length, and trends in phosphate content and zeta potential were elucidated. The CNC length could be tuned over a relatively large range (238-475 nm) and the polydispersity could be narrowed most effectively by increasing the hydrolysis temperature and acid concentration. The CNC phosphate content was most affected by hydrolysis temperature and time; however, the charge density and colloidal stability were considered low compared with sulfuric acid hydrolysed CNCs. This study provides insight into weak acid hydrolysis and proposes `design rules' for CNCs with improved size uniformity and charge density. This article is part of a discussion meeting issue `New horizons for cellulose nanotechnology'.

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

    International Nuclear Information System (INIS)

    Pierce, R.A.; Smith, J.R.; Poprik, D.C.

    1995-01-01

    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

  9. Study of phosphoric acid crystallization using a focused beam reflectance measurement method

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Yong [School of Chemistry and Resource Environment, Linyi Normal University, Linyi Shandong 276005 (China); Chen, Kui; Wu, Yanyang; Zhu, Jiawen [Chemical Engineering Research Center, East China University of Science and Technology, Shanghai 200237 (China); Sheng, Yong [SINOCHEN Fuling Chemical Industrial Co., Ltd, Chongqing 226005 (China)

    2010-10-15

    A way for restoring the crystal size distributions (CSD) from measured chord length distributions (CLD) was reported in this paper. The kinetics of phosphoric acid crystallization process was investigated in cooling mode using focused beam reflectance measurement (FBRM) and digital photo technique. In order to restore the CSD from measured CLD and verify the reliability of FBRM data, digital photo technique in real time and optical microscope were applied in large crystal size and small range, respectively. Results indicated a converting constant A existed between CLD and CSD when crystal growth follows size-independent growth (Mcabe's {delta}L law) law. It was verified by Malvern particles size analysis method. The converting constant A varied with crystal morphology. The crystal growth order increased with the stirring increasing speed during phosphoric acid crystallization process. The trend was especially notable at higher speed situations. It can illustrate that the state of phosphoric acid hemihydrate crystal growth was controlled by both diffusion and surface-integration with the increasing stirring speed. (copyright 2010 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim) (orig.)

  10. Interim solidification of SRP waste with silica, bentonite, or phosphoric acid

    International Nuclear Information System (INIS)

    Thompson, G.H.

    1976-03-01

    One option for interim waste management at the Savannah River Plant is in-tank solidification of the liquid waste solutions. This would reduce the mobility of these highly radioactive solutions until techniques for their long-term immobilization and storage are developed and implemented. Interim treatments must permit eventual retrieval of waste and subsequent incorporation into a high-integrity form. This study demonstrated the solidification of simulated alkaline waste solutions by reaction with silica, bentonite, and phosphoric acid. Alkaline waste can be solidified by reaction with silica gel, silica flour, or sodium silicate solution. Solidified products containing waste salt can be retrieved by slurrying with water. Alkaline supernate (solution in equilibrium with alkaline sludge in SRP waste tanks) can be solidified by reaction with bentonite to form cancrinite powder. The solidified waste can be retrieved by slurrying with water. Alkaline supernate can be solidified by partial evaporation and reaction with phosphoric acid. Water is incorporated into hydrated complexes of trisodium phosphate. The product is soluble, but actual plant waste would not solidify completely because of decay heat. Reaction of simulated alkaline waste solutions with silica gel, silica flour, or bentonite increases the volume by a factor of approximately 6 over that of evaporated waste; reaction with phosphoric acid results in a volume 1.5 times that of evaporated waste. At present, the best method for in-tank solidification is by evaporation, a method that contributes no additional solids to the waste and does not compromise any waste management options

  11. Extractants for uranium recovery from wet phosphoric acid

    International Nuclear Information System (INIS)

    Musikas, C.; Benjelloun, N.; Lours, S.

    1981-08-01

    It must be pointed out that despite their lower affinity for uranyl, the dialkyldithiophosphates show higher extraction coefficients than dialkylphosphates. In addition, it is possible to back extract uranium with oxalate solutions at pH levels where the solvents remain in their acidic form. This last possibility seems to be correlated with the presence of a H 2 PO 4 - ion in the U(VI) organic complexes

  12. Electrochemistry of Phosphorous and Hypophosphorous Acid on a Pt electrode

    International Nuclear Information System (INIS)

    Prokop, M.; Bystron, T.; Bouzek, K.

    2015-01-01

    Highlights: • H 3 PO 3 and H 3 PO 2 oxidation on Pt electrode proceed at high overpotential. • H 3 PO 2 oxidation proceeds via H 3 PO 3 as intermediate. • H 3 PO 3 and H 3 PO 2 adsorb on Pt electrode, adsorption isotherms determined. • Adsorption is more pronounced at elevated temperature. • Tautomeric equilibria plays an important role in the acids behaviour. - Abstract: H 3 PO 4 is commonly used as a proton-conducting phase in high temperature proton exchange membrane fuel cell membranes. However, its reduction with hydrogen at elevated temperatures yields compounds like H 3 PO 3 and phosphorus. The aim of this work was to describe the basic electrochemical behaviour of H 3 PO 3 and H 3 PO 2 on a Pt electrode in diluted aqueous H 2 SO 4 solutions. The results show that adsorption of both phosphorus acids studied becomes important at an oxoacid bulk concentration around and below 10 mol dm −3 . Adsorption isotherms at 25 and 70 °C were determined for both acids. Unusually, the extent of adsorption increases with rising temperature. H 3 PO 3 is anodically oxidised on a bare Pt as well as on a PtO surface. H 3 PO 2 oxidation proceeds mainly on a PtO surface, with the intermediate product being H 3 PO 3 . High overvoltage around 1 V is characteristic of all anodic oxidation reactions occurring in the temperature range studied

  13. Porous structure and surface chemistry of phosphoric acid activated carbon from corncob

    Science.gov (United States)

    Sych, N. V.; Trofymenko, S. I.; Poddubnaya, O. I.; Tsyba, M. M.; Sapsay, V. I.; Klymchuk, D. O.; Puziy, A. M.

    2012-11-01

    Active carbons have been prepared from corncob using chemical activation with phosphoric acid at 400 °C using varied ratio of impregnation (RI). Porous structure of carbons was characterized by nitrogen adsorption and scanning electron microscopy. Surface chemistry was studied by IR and potentiometric titration method. It has been shown that porosity development was peaked at RI = 1.0 (SBET = 2081 m2/g, Vtot = 1.1 cm3/g), while maximum amount of acid surface groups was observed at RI = 1.25. Acid surface groups of phosphoric acid activated carbons from corncob includes phosphate and strongly acidic carboxylic (pK = 2.0-2.6), weakly acidic carboxylic (pK = 4.7-5.0), enol/lactone (pK = 6.7-7.4; 8.8-9.4) and phenol (pK = 10.1-10.7). Corncob derived carbons showed high adsorption capacity to copper, especially at low pH. Maximum adsorption of methylene blue and iodine was observed for carbon with most developed porosity (RI = 1.0).

  14. Optimization of Butylphosphate synthesis from O-Phosphoric Acid

    International Nuclear Information System (INIS)

    Amedjkouh, A.; Attou, M.; Azzouz, A.; Zaoui, B.

    1995-07-01

    This work was carried out in order to confirm results of previous work and to enhance the yield of TBP synthesis. This, many reactions have been realised under differents experimental condition (temperature, acid/ alcool molar ratio, pressure and the quantity of promoter agent 'POCL3'). the TBP yield variations as function the experimental parameters, has been expressed, using the 2n factorial plan mathematical model. The experimental results were compared to those given by the theoritical model, and the optimal conditions were then drawn out

  15. Amino-Functional Polybenzimidazole Blends with Enhanced Phosphoric Acid Mediated Proton Conductivity as Fuel Cell Electrolytes

    DEFF Research Database (Denmark)

    Aili, David; Javakhishvili, Irakli; Han, Junyoung

    2016-01-01

    A new amino-functional polybenzimidazole copolymer is synthesized by homogeneous solution condensation polymerization from a novel monomer, N,N′-bis (2,4-diaminophenyl)-1,3-diaminopropane. The copolymer readily dissolves in organic solvents and shows good film forming characteristics. To balance...... the phosphoric acid uptake and to obtain mechanically robust membranes, the amino-functional polybenzimidazole derivative is blended with high molecular weight poly [2,2′-(m-phenylene)-5,5′-bisbenzimidazole] at different ratios. Due to the high acid uptake, the homogenous blend membranes show enhanced proton...

  16. Use of a pulsed column with discs and crowns for uranium extraction from phosphoric acid

    International Nuclear Information System (INIS)

    1982-04-01

    The physico-chemistry of the system phosphoric acid-uranium-dioctylpyrophosphoric acid is studied for the determination of analytical methods and extraction parameters (oxidation state of uranium and iron, phosphorus concentration, extractant concentration). Extraction is then realized on a pilot scale with a liquid-liquid extraction column 4m high and of 50 mm in diameter with a column packing made of discs and crowns. Column efficiency is evaluated by studying uranium transfer as a function of operating conditions. The results obtained are extrapolated to an industrial scale and a comparative economic evaluation is made between a pulsed column and a mixer-settler [fr

  17. The Comparison of Hydrochloric Acid and Phosphoric Acid Treatments in the Preparation of Montmorillonite Catalysts for RNA Synthesis

    Science.gov (United States)

    Aldersley, Michael Frank; Joshi, Prakash C.; Huang, Yixing

    2017-09-01

    The treatment of clay minerals with a preliminary acid wash and titration to pH 7 has proven to generate catalysts for the most interesting of oligomerization reactions in which activated RNA-nucleotides generate oligomers up to 40-mers. Significantly, not all clay minerals become catalytic following this treatment and none are catalytic in the absence of such treatment. The washing procedure has been modified and explored further using phosphoric acid and the outcomes are compared to those obtained when clay samples are prepared following a hydrochloric acid wash.

  18. The Comparison of Hydrochloric Acid and Phosphoric Acid Treatments in the Preparation of Montmorillonite Catalysts for RNA Synthesis.

    Science.gov (United States)

    Aldersley, Michael Frank; Joshi, Prakash C; Huang, Yixing

    2017-09-01

    The treatment of clay minerals with a preliminary acid wash and titration to pH 7 has proven to generate catalysts for the most interesting of oligomerization reactions in which activated RNA-nucleotides generate oligomers up to 40-mers. Significantly, not all clay minerals become catalytic following this treatment and none are catalytic in the absence of such treatment. The washing procedure has been modified and explored further using phosphoric acid and the outcomes are compared to those obtained when clay samples are prepared following a hydrochloric acid wash.

  19. Physical-Mechanical Properties and Micromorphology of Calcium Cements Exposed to Polyacrylic and Phosphoric Acids.

    Science.gov (United States)

    de Souza, Gustavo Fernandes; Arrais, Ana Beatriz; Aragão, Cícero Flávio Soares; Ferreira, Isana Alvares; Borges, Boniek Castillo Dutra

    2018-01-01

    To evaluate if physical and mechanical properties of self-curing calcium hydroxide cements were affected by contact with polyacrylic and phosphoric acids. Resin-containing (Life (LF)) and resin-free (Hydro C (HyC)) materials were subjected to polyacrylic acid conditioning and rinsing (POL); phosphoric acid conditioning and rinsing (PHO); rinsing only; and no treatment ( n = 10). Water sorption/solubility, release of hydroxyl ions (pH), roughness (Ra), and impact resistance were evaluated. Additional samples ( n = 1) were prepared for scanning electron microscopy (SEM) analysis of the surface morphology. Data were analyzed by two-way ANOVA and Tukey post hoc test ( P < 0.05). Water sorption was significantly higher for LF when in contact with PHO and lower for POL ( P < 0.05). The mean solubility was higher with POL for both cements ( P < 0.05). PHO increased the mean surface roughness for HyC ( P < 0.01); a significant decrease was noted for LF after contact with both acids ( P < 0.01). PHO promoted lower release of hydroxyl ions on both cements ( P < 0.05). For LF, rinsing, PHO, and POL presented similar morphology, differing from the control group. For HyC, PHO and POL presented similar morphology, differing from the control group. PHO had a negative effect on the physical properties of the cements tested, except for the solubility test. POL affected roughness and solubility of HyC cement. Clinical procedures that require polyacrylic and phosphoric acid conditioning must be done carefully on self-curing calcium hydroxide cements in order to avoid negative impact on their properties.

  20. The extraction of uranium from wet process phosphoric acid using a liquid surfactant membrane system

    International Nuclear Information System (INIS)

    Dickens, N.; Davies, G.A.

    1984-01-01

    A liquid membrane extraction process is examined for the extraction of uranium from wet process phosphoric acid. Uranium is present in the acid in concentrations up to 100 ppm which in principle makes it ideal for treatment with a membrane process. The membrane system studied is based on extraction using DEHPA-TOPO reagents which are contained within the organic phase of a water in oil emulsion. Formulations of the emulsion membrane system have been studied, the limitations of acid temperature, P 2 O 5 concentration and solid dispersed impurities in the acid have been studied in laboratory batch experiments and in a continuous pilot plant unit capable of treating 5l of concentrated acid per minute. Data from the pilot plant work has been used to develop a flowsheet for a commercial unit based on this process. (author)

  1. Wet Chemical Oxidation of Organic Waste Using Nitric-Phosphoric Acid Technology

    Energy Technology Data Exchange (ETDEWEB)

    Pierce, R.A.

    1998-10-06

    Experimental progress has been made in a wide range of areas which support the continued development of the nitric-phosphoric acid oxidation process for combustible, solid organic wastes. An improved understanding of the overall process operation has been obtained, acid recovery and recycle systems have been studied, safety issues have been addressed, two potential final waste forms have been tested, preliminary mass flow diagrams have been prepared, and process flowsheets have been developed. The flowsheet developed is essentially a closed-loop system which addresses all of the internally generated waste streams. The combined activities aim to provide the basis for building and testing a 250-400 liter pilot-scale unit. Variations of the process now must be evaluated in order to address the needs of the primary customer, SRS Solid Waste Management. The customer is interested in treating job control waste contaminated with Pu-238 for shipment to WIPP. As a result, variations for feed preparation, acid recycle, and final form manufacturing must be considered to provide for simpler processing to accommodate operations in high radiation and contamination environments. The purpose of this program is to demonstrate a nitric-phosphoric acid destruction technology which can treat a heterogeneous waste by oxidizing the solid and liquid organic compounds while decontaminating noncombustible items.

  2. Production of activated carbon from peanut hill using phosphoric acid and microwave activation

    Directory of Open Access Journals (Sweden)

    Weerawat Clowutimon

    2015-06-01

    Full Text Available The optimum conditions for preparing activated carbon from peanut hulls by phosphoric acid and microwave activation were studied. Factors investigated in this study were temperature of carbonization at 300, 350, 400 and 450๐ C, and time of carbonization at 30, 60 and 90 minutes. The optimum yield was observed that carbonization temperature of 400๐ C and time at 60 minutes, respectively. The yield of charcoal was 39% and the f ix carbon was 69%. Then the charcoal was activated by phosphoric acid and microwave irradiation, respectively. The effect of the weight per volume ratios of charcoal to activating acid (1:1, 1:2 and 2:1(W/V, microwave power at (activated 300, 500 and 700 watts, and activated time (30, 60 and 90 seconds were studied. The results showed that the optimum conditions for activating peanut charcoal were 1:2 (W/V charcoal per activating acid, microwave power 700 watts for 90 seconds. The results yielding maximum surface area by BET method was 303.1 m2 /g and pore volume was 0.140 cm3 /g. An efficiency of maximum iodine adsorption was 418 mg iodine/g activated carbon. Comparing the adsorption efficiency of non- irradiated and irradiated activated carbon, the efficiency of irradiated activated carbon improved up to 31%, due to its larger surface area and pore volume.

  3. Unexpected 226Ra build-up in wet-process phosphoric-acid plants

    International Nuclear Information System (INIS)

    Lardinoye, M.H.; Weterings, K.; Berg, W.B. van de

    1982-01-01

    During an investigation of the distribution of radium and uranium over the different process streams in phosphoric-acid production and in the nitrophosphate route, a higher than average radiation level was detected in the vicinity of some piping and vessels near the gypsum filters. This higher radiation level is caused by radium which is present in very low concentrations in the phosphates used for fertilizer production. Detectable radiation levels around vessels and piping in other phosphoric-acid works have since been determined. In all factories the filter part and especially the washing-acid section showed the highest radiation level. In the piping of the gypsum filter, through which the washing acid is discharged, a scaling of barium sulphate and calcium sulphate with a higher radium concentration is formed. The radium ions appeared to be incorporated in the barium sulphate lattice, hence the solubility of the radium precipitate is very low. The danger of internal contamination in cleaning operations by radioactive intake or inhalation of radon is very small in the cases described. The risk of external radiation can be prevented by periodically cleaning the equipment in which the radioactive scaling is formed. (author)

  4. Unexpected /sup 226/Ra build-up in wet-process phosphoric-acid plants

    Energy Technology Data Exchange (ETDEWEB)

    Lardinoye, M.H.; Weterings, K. (Stamicarbon B.V., Geleen (Netherlands)); van de Berg, W.B. (Unie van Kunstmestfabrieken, Utrecht (Netherlands))

    1982-04-01

    During an investigation of the distribution of radium and uranium over the different process streams in phosphoric-acid production and in the nitrophosphate route, a higher than average radiation level was detected in the vicinity of some piping and vessels near the gypsum filters. This higher radiation level is caused by radium which is present in very low concentrations in the phosphates used for fertilizer production. Detectable radiation levels around vessels and piping in other phosphoric-acid works have since been determined. In all factories the filter part and especially the washing-acid section showed the highest radiation level. In the piping of the gypsum filter, through which the washing acid is discharged, a scaling of barium sulphate and calcium sulphate with a higher radium concentration is formed. The radium ions appeared to be incorporated in the barium sulphate lattice, hence the solubility of the radium precipitate is very low. The danger of internal contamination in cleaning operations by radioactive intake or inhalation of radon is very small in the cases described. The risk of external radiation can be prevented by periodically cleaning the equipment in which the radioactive scaling is formed.

  5. Unexpected 226Ra build-up in wet-process phosphoric-acid plants.

    Science.gov (United States)

    Lardinoye, M H; Weterings, K; van de Berg, W B

    1982-04-01

    During an investigation of the distribution of radium and uranium over the different process streams in phosphoric-acid production and in the nitrophosphate route, a higher than average radiation level was detected in the vicinity of some piping and vessels near the gypsum filtres. This higher radiation level is caused by radium, which, as a decay product in the 238U series, is present in very low concentrations (1-50 pCi 226R/g) in the phosphates used for fertilizer production. Specific research later on established that there were detectable radiation levels around vessels and piping in other phosphoric-acid works as well. It turned out that in all factories the filter part, and especially the washing-acid section showed the highest radiation-level. In the piping of the gypsum filter, through which the washing acid is discharged, a scaling of bariumsulphate and calciumsulphate with a higher radiumconcentration (+/- 0.1 Ci/g) is formed. The radium ions appeared to be incorporated in the bariumsulphate lattice, hence the solubility of the radium precipitate is very low. The danger of internal pollution, for example in cleaning operations by radio-active intake or inhallation of radon is very small in the cases described. The risk of external radiation can be prevented by periodically cleaning (every 1-3 yr) the equipment in which the radio-active scaling is formed.

  6. Unexpected /sup 226/Ra build-up in wet-process phosphoric-acid plants

    Energy Technology Data Exchange (ETDEWEB)

    Lardinoye, M.H.; Weterings, K.; van de Berg, W.B.

    1982-04-01

    During an investigation of the distribution of radium and uranium over the different process streams in phosphoric-acid production and in the nitrophosphate route, a higher than average radiation level was detected in the vicinity of some piping and vessels near the gypsum filtres. This higher radiation level is caused by radium, which, as a decay product in the /sup 238/U series, is present in very low concentrations (1-50 pCi 226R/g) in the phosphates used for fertilizer production. Specific research later on established that there were detectable radiation levels around vessels and piping in other phosphoric-acid works as well. It turned out that in all factories the filter part, and especially the washing-acid section showed the highest radiation-level. In the piping of the gypsum filter, through which the washing acid is discharged, a scaling of bariumsulfate and calciumsulfate with a higher radium concentration (+/- 0.1 Ci/g) is formed. The radium ions appeared to be incorporated in the bariumsulphate lattice, hence the solubility of the radium precipitate is very low. The danger of internal pollution, for example in cleaning operations by radioactive intake or inhalation of radon is very small in the cases described. The risk of external radiation can be prevented by periodically cleaning (every 1-3 yr) the equipment in which the radioactive scaling is formed.

  7. Improvement of Haramay Fiber by Pre-treatment of Retting Process withPhosphoric Acid

    International Nuclear Information System (INIS)

    Kuntari-Sasas; Neni-Rustini Eriawati

    2000-01-01

    Haramay as bast fiber contains of cellulose fiber as the main part, mixedwith hemi cellulose, pectin, and lignin as binding material for cellulosefiber to keep it together in the bundle form. For textile material, this bastfiber has to be freed from its binding material, called as retting process,before subjecting to scouring, dyeing and finishing process in textileindustry. In the retting process the dissolve of binding material can be doneeither by using enzyme in bio technology or extraction with strong alkalinecondition in common technology. Using sodium hydroxide for dissolving thebinding material can be carried out easily with good dissolving ability, butcan render the strength retention of the cellulose fiber. Pre-treatment ofthe bast fiber with phosphoric acid (H 3 PO 4 ), is expected to hydrolyze someof the binding materials that can not be dissolved in alkaline condition,including natural pigment that colored the fiber with creamy white. In thisstudy, the pre-treatment process before retting with phosphoric acid wascarried out in various condition, such as concentration of phosphoric acid (5ml/l- 25 ml/l), time and temperature of pre-treatment (1-3 hours at 50 o C or12-24 hours at room temperature), followed by neutralization in dilutealkaline. The retting process was carried out by means of scouring in variousconcentration of sodium hydroxide (NaOH 38 o Be, 10 ml/l-30 m/l), and then wascontinued with bleaching process in hydrogen peroxide solution. Aftercarrying out those experiment, the bast fiber that called haramay wassubjected to testing for weight reduction, strength retention and degree ofwhiteness. From the testing results it is concluded that pre-treatment withphosphoric acid can increase the weight reduction, strength retention ortenacity and degree of whiteness of haramay fiber compared to the oneswithout pre-treatment with phosphoric acid. The best result was obtained bypre-treatment with 5 ml/l H 3 PO 4 at 50 o C for 2 hours, continued by

  8. Carbon components in the phosphoric acid fuel cell-an overview

    International Nuclear Information System (INIS)

    Appleby, J.

    1983-01-01

    The single breakthrough that has made the phosphoric acid fuel cell a practical reality has been the use of carbon or graphite components for the repeat parts of the cell stack. While the thermodynamic stability of carbon is such that rapid corrosion would be expected at the cathode at fuel cell operating temperature, its kinetic stability is remarkable despite the absence of passivating layers analogous to those on, for example, the Group VA elements niobium and tantalum. This happy accident, combined with the adequate electronic conductivity of the carbon materials used, has provided the opportunity to reduce fuel cell cost to attractive levels. The development of these carbon compounds is reviewed

  9. Photoluminescence emission of nanoporous anodic aluminum oxide films prepared in phosphoric acid

    Science.gov (United States)

    2012-01-01

    The photoluminescence emission of nanoporous anodic aluminum oxide films formed in phosphoric acid is studied in order to explore their defect-based subband electronic structure. Different excitation wavelengths are used to identify most of the details of the subband states. The films are produced under different anodizing conditions to optimize their emission in the visible range. Scanning electron microscopy investigations confirm pore formation in the produced layers. Gaussian analysis of the emission data indicates that subband states change with anodizing parameters, and various point defects can be formed both in the bulk and on the surface of these nanoporous layers during anodizing. PMID:23272786

  10. Hydrogen evolution activity and electrochemical stability of selected transition metal carbides in concentrated phosphoric acid

    DEFF Research Database (Denmark)

    Tomás García, Antonio Luis; Jensen, Jens Oluf; Bjerrum, Niels J.

    2014-01-01

    phosphoric acid were investigated in a temperature range from 80 to 170°C. A significant dependence of the activities on temperature was observed for all five carbide samples. Through the entire temperature range Group 6 metal carbides showed higher activity than that of the Group 5 metal carbides......Alternative catalysts based on carbides of Group 5 (niobium and tantalum) and 6 (chromium, molybdenum and tungsten) metals were prepared as films on the metallic substrates. The electrochemical activities of these carbide electrodes towards the hydrogen evolution reaction (HER) in concentrated...

  11. Separation of uranium and other metals from commercial phosphoric acid by ion-exchange and voltammetric determination of uranium

    International Nuclear Information System (INIS)

    Ferreira, J.B.C.; Carvalho, F.M.S. de; Abrao, A.

    1985-11-01

    The separation of metals from crude commercial phosphoric acid is achieved by simple dilution and percolation through a strong cationic ion exchanger. Uranium, calcium, magnesium, manganese, iron and aluminum are quantitatively fixed by the exchanger and can be detected or analysed after their complete elution with 6 M HCI. Titanium and zirconium are only partially retained. Specially for its separation and determination uranium is retained selectively by the resin from the phosphoric acid-EDTA solution, the column is washed with water and then eluted with hydrochloric acid. Uranium is analyzed by voltametry with the hanging drop mercury electrode. (Author) [pt

  12. Methyl phosphate formation as a major degradation mode of direct methanol fuel cells with phosphoric acid based electrolytes

    DEFF Research Database (Denmark)

    Aili, David; Vassiliev, Anton; Jensen, Jens Oluf

    2015-01-01

    Phosphoric acid and phosphoric acid doped polymer membranes are widely used as electrolytes in hydrogen based fuel cells operating at elevated temperatures. Such electrolytes have been explored for direct oxidation of methanol to further increase the versatility of the systems, however......, with demonstrated lifetimes of only a few days to weeks. In this work the methyl phosphate formation from the acid and methanol is identified and proposed to be a major mechanism for the cell degradation. Proton conductivity and fuel cell durability tests validate the mechanism at high methanol contents....

  13. Polymeric supported sorbents for decreasing hazardous metal ions content in wet process phosphoric acid

    International Nuclear Information System (INIS)

    El-Zahhar, A.A.; El-Naggar, H.A.; Ahmed, M.

    2005-01-01

    Procedure for preparation of polymeric supported silica, and their usage for decreasing hazardous metal ion content in wet process phosphoric acid was developed. The procedure is based firstly on extraction silica from rice straw by alkaline treatment , secondly supporting the produced silica on binding polyacrylonitrile (PAN). The produced polymer based sorbent was used for decreasing hazardous metal ions (especially iron) present as inorganic impurities in crud Egyptian phosphoric acid (green acid). Different factors affecting the sorption equilibrium ( contact time, temperature , sorbent mass and batch factor ) were studied. Studying the sorption isotherm revealed that the adsorption data could favorably fit the Langmuir adsorption isotherm. In the dynamic study , the sorption capacity at (Cξ/Cο = 50%) was found to be 28.5 mg/g and the loaded column could be regenerated using 50ml of 0.15 M HNO 3 . The regenerated column could undergo sorption regeneration cycles up to four cycles without significant decrease in the sorption capacity , weight loss or change in the physical properties of the sorbent

  14. Limiting Current of Oxygen Reduction on Gas-Diffusion Electrodes for Phosphoric Acid Fuel Cells

    DEFF Research Database (Denmark)

    Li, Qingfeng; Gang, Xiao; Hjuler, Hans Aage

    1994-01-01

    on polytetrafluorine-ethyl bonded gas-diffusion electordes in phosphoric acid with and without fluorinated additives. This provides an alternative to estimate the film thickness by combining it with the acid-adsorption measurements and the porosity analysis of the catalyst layer. It was noticed that the limiting......Various models have been devoted to the operation mechanism of porous diffusion electrodes. They are, however, suffering from the lack of accuracy concerning the acid-film thickness on which they are based. In the present paper the limiting current density has been measured for oxygen reduction...... current density can be accomplished either by gas-phase diffusion or liquid-phase diffusion, and it is the latter that can be used in the film-thickness estimation. It is also important to mention that at such a limiting condition, both the thin-film model and the filmed agglomerate model reach the same...

  15. Thermal Effect on the phosphoric Acid Impregnated Activated Carbon Fiber and Adsorption Properties Toward Isoprene

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, Taek Sung; Lee, Jin Hyok; Kang, Kyung suk [Department of Chemical Engineering, College of Engineering, Chungnam National University, Taejon (Korea); Kim, Kwang Young [Ace Lab. Co. Ltd. Taejon (Korea); Rhee, Moon Soo [Korea Ginseng and Tobacoo Research Institute, Taejon (Korea)

    2001-05-01

    To introduce chemisorption property and improve adsorption capacities for isoprene, ACF (Activated Carbon Fiber) was impregnated by phosphoric acid. As the impregnated ACF was dried by programmed temperature from 300 degree C to 500 degree C, degree of impregnation, surface area, thermal stability and adsorption properties for isoprene were observed. The degree of impregnation of the ACF, dried at the 400 degree C, was 12.7 w/w% and surface area was 1148 m{sup 2}/g. Over the temperature range of 450 degree C to 700 degree C, there was one-step thermal degradation by the thermal decomposition of phosphonyl group. The adsorption rate of phosphoric acid on the impregnated ACF, which was dried at 400 degree C, was the fastest. The breakthrough time of ACF that was dried at 400 degree C was 18 min., and its adsorption capacity improved roughly 7.2 times in comparison to the pure ACF. In addition, it was observed the adsorption properties persisted even after the regeneration. The adsorption efficiency of regenerated ACF was 66 percent compared to the unused impregnated ACF. 21 refs., 7 figs., 3 tabs.

  16. Catalyst evaluation for oxygen reduction reaction in concentrated phosphoric acid at elevated temperatures

    Science.gov (United States)

    Hu, Yang; Jiang, Yiliang; Jensen, Jens Oluf; Cleemann, Lars N.; Li, Qingfeng

    2018-01-01

    Phosphoric acid is the common electrolyte for high-temperature polymer electrolyte fuel cells (HT-PEMFCs) that have advantages such as enhanced CO tolerance and simplified heat and water management. The currently used rotating disk electrode technique is limited to tests in dilute solutions at low temperatures and hence is not suitable for catalyst evaluation for HT-PEMFCs. In this study, we have designed and constructed a half-cell setup to measure the intrinsic activities of catalysts towards the oxygen reduction reaction (ORR) in conditions close to HT-PEMFC cathodes. By optimization of the hydrophobic characteristics of electrodes and the catalyst layer thickness, ORR activities of typical Pt/C catalysts are successfully measured in concentrated phosphoric acid at temperatures above 100 °C. In terms of mass-specific activities, the catalyst exhibits about two times higher activity in the half-cell electrode than that observed in fuel cells, indicating the feasibility of the technique as well as the potential for further improvement of fuel cell electrode performance.

  17. Solid phosphoric acid oligomerisation: Manipulating diesel selectivity by controlling catalyst hydration

    International Nuclear Information System (INIS)

    Prinsloo, Nicolaas M.

    2006-01-01

    Solid phosphoric acid (SPA) catalyst is traditionally used in crude oil refineries to produce unhydrogenated motor-gasoline by propene and butene oligomerisation. SPA is also used in High-Temperature Fischer-Tropsch refineries (HTFT) to produce synthetic fuels albeit with a different emphasis. The petrol/diesel ratio of an HTFT refinery is very different from crude refining and it is often necessary to shift this ratio depending on market requirements. The influence of hydration was investigated as a means of improving diesel selectivity. This was achieved by studying SPA over a hydration range of 99-110% H 3 PO 4 , a temperature range of 140-230 o C and using C 3 -C 6 model and synthetic FT-derived olefinic feedstocks. A direct correlation was found between the selectivity towards diesel range products and the distribution of the phosphoric acid species viz. H 3 PO 4 , H 4 P 2 O 7 and H 5 P 3 O 10 . For various olefinic feedstocks, diesel selectivity increased with decreasing catalyst hydration with a maximum around 108% H 3 PO 4 for propene oligomerisation. Commercial tests confirmed the increase in diesel selectivity with lowered catalyst hydration. (author)

  18. Synthesis of a chelate resin with amido and phosphoric acid and its character in uranium extraction

    International Nuclear Information System (INIS)

    Qiu Yueshuang; Zhang Jianguo; Feng Yu; Zhao Chaoya

    2013-01-01

    A chelate resin (D814) with amido and phosphoric acid functional group was synthetized by means of the reactions of stytene-divinyl benzene chloromethylated sphere with ethylenedianmine and orth-phosphorous acid and formaldehyde. This resin can be used to adsorb uranium from leaching solution with high chloride ion in the rang of pH l.33-9.05, and the adsorption rate of uranium was above 95%. D814 resin had a good ability resistant to high chloride ion. The loading capacity for uranium was not apparently effected when chlorid ion concentration in solution was 60 g/L. The results of the adsorption experiment show that when the ratio of saturation volume to breakthrough volume was l.82, the uranium saturation capacity of D814 was 40.5 mg/g dry resin. NaCl + NaHCO 3 was used for eluting agent, and the eluting rate of uranium was 96.7%. Adsorption uranium mechanism by D814 was also discussed. (authors)

  19. Study of corrosion-erosion behaviour of stainless alloys in industrial phosphoric acid medium

    International Nuclear Information System (INIS)

    Guenbour, Abdellah; Hajji, Mohamed-Adil; Jallouli, El Miloudi; Bachir, Ali Ben

    2006-01-01

    The corrosion and corrosion-abrasion resistance of some stainless steels in industrial phosphoric acid 30% P 2 O 5 has been studied using electrochemical techniques. The corrosion rate of materials increases with the increase of temperature. Alloys which contain chromium, molybdenum and nitrogen in sufficient quantities present the best behaviour. In the abrasion-corrosion conditions, the experimental device set up allowed to follow continually samples electrochemical behaviour. Under dynamic conditions and without solid particles, the increase of acid projection speed has no effect on the alloys corrosion behaviour. The adding of abrasive leads to a general increase of corrosion rate and to a decrease of material resistance. Under these conditions, materials attack is controlled by synergistic effect between the abrasion and the impurities. The cast 30% Cr shows good resistance according to his high chromium content

  20. Purification of Industrial Phosphoric Acid using Silica Produced from Rice Husk (Part 1)

    International Nuclear Information System (INIS)

    Gad, H.M.H.; Awwad, N.S.; El-Khalafawy, A.; Daifullah, A.A.M.; El-Reefy, S.A.; Aly, H.F.

    2008-01-01

    In this work, silica was extracted from rice husk (RH) by different techniques and used for removal of some heavy metals from industrial phosphoric acid. The data obtained, showed that removal of Cu(II), Cd(II) and Pb(II) is efficient when the silica used is obtained by acidic treatment, while the removal of Fe(III) and Zn(II) is efficient when the silica used was obtained by alkaline treatment of RH. On the other hand, if silica used is obtained from rice husk ash (RHA) it was found more efficient for the removal of Mn. In all cases, the concentration of silica has been characterized by UV-Spectrophotometry. FTIR, SEM and EDX were used for predication of sorption mechanism

  1. Study of corrosion-erosion behaviour of stainless alloys in industrial phosphoric acid medium

    Energy Technology Data Exchange (ETDEWEB)

    Guenbour, Abdellah [Laboratory of Electrochemistry-Corrosion, Av. Ibn Batouta, BP1014-Faculty of Science, Rabat (Morocco)]. E-mail: guenbour@fsr.ac.ma; Hajji, Mohamed-Adil [Group Corrosion and Protection of Materials, ENIM, Rabat (Morocco); Jallouli, El Miloudi [Group Corrosion and Protection of Materials, ENIM, Rabat (Morocco); Bachir, Ali Ben [Laboratory of Electrochemistry-Corrosion, Av. Ibn Batouta, BP1014-Faculty of Science, Rabat (Morocco)

    2006-12-30

    The corrosion and corrosion-abrasion resistance of some stainless steels in industrial phosphoric acid 30% P{sub 2}O{sub 5} has been studied using electrochemical techniques. The corrosion rate of materials increases with the increase of temperature. Alloys which contain chromium, molybdenum and nitrogen in sufficient quantities present the best behaviour. In the abrasion-corrosion conditions, the experimental device set up allowed to follow continually samples electrochemical behaviour. Under dynamic conditions and without solid particles, the increase of acid projection speed has no effect on the alloys corrosion behaviour. The adding of abrasive leads to a general increase of corrosion rate and to a decrease of material resistance. Under these conditions, materials attack is controlled by synergistic effect between the abrasion and the impurities. The cast 30% Cr shows good resistance according to his high chromium content.

  2. Ion flotation of uranium contained in industrial phosphoric acid with collector recycling

    International Nuclear Information System (INIS)

    Jdid, E.; Blazy, P.; Bessiere, J.

    1985-01-01

    Uranium has been recovered from wet-process phosphoric acid (30% P 2 O 5 ) by ion flotation with an anionic organophosphorous collector. Recoveries greater than 90% were obtained even at temperatures of about 60 C, the uranium concentrate, which was collected in the froth as a precipitate, containing 7 to 10% U. Collector consumption without recycling of the surface-active reagent was about 12 kg/kg U. Much of the reagent, however, can be recovered for recycling by attack with sodium hydroxide on the floated phase after filtration. This enables a precipitate containing about 30% U to be produced and decreases collector consumption to about 3 kg/kg U. The results were obtained in laboratory-scale experiments on industrial wet-process acid. (author)

  3. 230Th, 232Th and 238U determinations in phosphoric acid fertilizer and process products by ICP-MS

    International Nuclear Information System (INIS)

    Nascimento, Marcos R.L. do; Guerreiro, Luisa M.R.; Bonifacio, Rodrigo L.; Taddei, Maria H.T.

    2015-01-01

    Through processing of Santa Quiteria-CE mine phosphate rock, Brazil has established a project for production of phosphoric acid fertilizer and uranium as a by-product. Under leaching conditions of phosphate rock with sulfuric acid, which is the common route for preparing phosphoric acid fertilizer, a large part of uranium, thorium and their decay products naturally present in the rock are solubilized. In order to assess the contamination potential in phosphoric acid and others process products, this paper describes a previous precipitation and direct methods for routine analysis of thorium and uranium isotopes by ICP-MS. In all samples, 230 Th, 232 Th and 238 U were directly determined after dilution, except 230 Th in phosphoric acid loaded with uranium sample, which to overcome equipment contamination effect, was determined after its separation by oxalate precipitation using lanthanum as a carrier. The results obtained by the proposed method by ICP-MS, were in good agreement when compared to alpha spectrometry for 230 Th, and ICP-OES and spectrophotometry with arsenazo III for elementary uranium and thorium determinations. (author)

  4. Process for the removal of acid forming gases from exhaust gases and production of phosphoric acid

    Science.gov (United States)

    Chang, Shih-Ger; Liu, David K.

    1992-01-01

    Exhaust gases are treated to remove NO or NO.sub.x and SO.sub.2 by contacting the gases with an aqueous emulsion or suspension of yellow phosphorous preferably in a wet scrubber. The addition of yellow phosphorous in the system induces the production of O.sub.3 which subsequently oxidizes NO to NO.sub.2. The resulting NO.sub.2 dissolves readily and can be reduced to form ammonium ions by dissolved SO.sub.2 under appropriate conditions. In a 20 acfm system, yellow phosphorous is oxidized to yield P.sub.2 O.sub.5 which picks up water to form H.sub.3 PO.sub.4 mists and can be collected as a valuable product. The pressure is not critical, and ambient pressures are used. Hot water temperatures are best, but economics suggest about 50.degree. C. The amount of yellow phosphorus used will vary with the composition of the exhaust gas, less than 3% for small concentrations of NO, and 10% or higher for concentrations above say 1000 ppm. Similarly, the pH will vary with the composition being treated, and it is adjusted with a suitable alkali. For mixtures of NO.sub.x and SO.sub.2, alkalis that are used for flue gas desulfurization are preferred. With this process, better than 90% of SO.sub.2 and NO in simulated flue gas can be removed. Stoichiometric ratios (P/NO) ranging between 0.6 and 1.5 were obtained.

  5. Effect of EDTA and phosphoric Acid pretreatment on the bonding effectiveness of self-etch adhesives to ground enamel.

    Science.gov (United States)

    Ibrahim, Ihab M; Elkassas, Dina W; Yousry, Mai M

    2010-10-01

    This in vitro study determined the effect of enamel pretreatment with phosphoric acid and ethylenediaminetetraacetic acid (EDTA) on the bond strength of strong, intermediary strong, and mild self-etching adhesive systems. Ninety sound human premolars were used. Resin composite cylinders were bonded to flat ground enamel surfaces using three self-etching adhesive systems: strong Adper Prompt L-Pop (pH=0.9-1.0), intermediary strong AdheSE (pH=1.6-1.7), and mild Frog (pH=2). Adhesive systems were applied either according to manufacturer instructions (control) or after pretreatment with either phosphoric acid or EDTA (n=10). After 24 hours, shear bond strength was tested using a universal testing machine at a cross-head speed of 0.5 mm/minute. Ultra-morphological characterization of the surface topography and resin/enamel interfaces as well as representative fractured enamel specimens were examined using scanning electron microscopy (SEM). Neither surface pretreatment statistically increased the mean shear bond strength values of either the strong or the intermediary strong self-etching adhesive systems. However, phosphoric acid pretreatment significantly increased the mean shear bond strength values of the mild self-etching adhesive system. SEM examination of enamel surface topography showed that phosphoric acid pretreatment deepened the same etching pattern of the strong and intermediary strong adhesive systems but converted the irregular etching pattern of the mild self-etching adhesive system to a regular etching pattern. SEM examination of the resin/enamel interface revealed that deepening of the etching pattern was consistent with increase in the length of resin tags. EDTA pretreatment had a negligible effect on ultra-morphological features. Use of phosphoric acid pretreatment can be beneficial with mild self-etching adhesive systems for bonding to enamel.

  6. Performance Degradation Tests of Phosphoric Acid Doped Polybenzimidazole Membrane Based High Temperature Polymer Electrolyte Membrane Fuel Cells

    DEFF Research Database (Denmark)

    Zhou, Fan; Araya, Samuel Simon; Grigoras, Ionela

    2015-01-01

    Degradation tests of two phosphoric acid (PA) doped PBI membrane based HT-PEM fuel cells were reported in this paper to investigate the effects of start/stop and the presence of methanol in the fuel to the performance degradation of the HT-PEM fuel cell. Continuous tests with pure dry H2 and meth...

  7. Temperature dependence and P/Ti ratio in phosphoric acid treatment of titanium dioxide and powder properties.

    Science.gov (United States)

    Onoda, H; Matsukura, A

    2015-02-01

    Titanium dioxide has photocatalytic activity and is used as a white pigment for cosmetics. A certain degree of sebum on the skin is decomposed by the ultraviolet radiation in sunlight. In this work, titanium dioxide was shaken with phosphoric acid to synthesize a white pigment for cosmetics. Titanium dioxide was treated with 0.1 mol/L of phosphoric acid at various P/Ti molar ratios, and then shaken in hot water for 1 h. The chemical composition, powder properties, photocatalytic activity, colour phase, and smoothness of the obtained powder were studied. The obtained materials indicated XRD peaks of titanium dioxide, however the peaks diminished subsequent to phosphoric acid treatment. The samples included small particles with sub-micrometer size. The photocatalytic activity of the obtained powders decreased, decomposing less sebum on the skin. Samples prepared at high P/Ti ratio with high shaking temperature indicated low whiteness in in L*a*b* colour space. The shaking and heating temperature and P/Ti ratio had influence on the smoothness of the obtained materials. Phosphoric acid treatment of titanium dioxide is an effective method to inhibit photocatalytic activity for a white pigment. © 2014 Society of Cosmetic Scientists and the Société Française de Cosmétologie.

  8. Efficacy of fungicide combinations, phosphoric acid, and plant extract from stinging nettle on potato late blight management and tuber yield

    Science.gov (United States)

    Late blight, caused by Phytophthora infestans is a major constraint to potato production. Inadequate management of the disease has often resulted in heavy losses in various production regions. We assessed the efficacy of fungicides, phosphoric acid, and stinging nettle plant extract combinations for...

  9. Study of a Triazole Derivative as Corrosion Inhibitor for Mild Steel in Phosphoric Acid Solution

    Directory of Open Access Journals (Sweden)

    Lin Wang

    2012-01-01

    Full Text Available The corrosion inhibition by a triazole derivative (PAMT on mild steel in phosphoric acid (H3PO4 solution has been investigated by weight loss and polarization methods. The experimental results reveal that the compound has a significant inhibiting effect on the corrosion of steel in H3PO4 solution. It also shows good corrosion inhibition at higher concentration of H3PO4. Potentiodynamic polarization studies have shown that the compound acts as a mixed-type inhibitor retarding the anodic and cathodic corrosion reactions with predominant effect on the cathodic reaction. The values of inhibition efficiency obtained from weight loss and polarization measurements are in good agreement. The adsorption of this compound is found to obey the Langmuir adsorption isotherm. Some kinetic and thermodynamic parameters such as apparent activation energy, frequency factor, and adsorption free energy have been calculated and discussed.

  10. Trial operation of a phosphoric acid fuel cell (PC25) for CHP applications in Europe

    Energy Technology Data Exchange (ETDEWEB)

    Uhrig, M.; Droste, W.; Wolf, D. [Ruhrgas AG, Dorsten (Germany)

    1996-12-31

    In Europe, ten 200 kW phosphoric acid fuel cells (PAFCs) produced by ONSI (PC25) are currently in operation. Their operators collaborate closely in the European Fuel Cell Users Group (EFCUG). The experience gained from trial operation by the four German operators - HEAG, HGW/HEW, Thyssengas and Ruhrgas - coincides with that of the other European operators. This experience can generally be regarded as favourable. With a view to using fuel cells in combined heat and power generation (CHP), the project described in this report, which was carried out in cooperation with the municipal utility of Bochum and Gasunie of the Netherlands, aimed at gaining experience with the PC 25 in field operation under the specific operating conditions prevailing in Europe. The work packages included heat-controlled operation, examination of plant behavior with varying gas properties and measurement of emissions under dynamic load conditions. The project received EU funding under the JOULE programme.

  11. 3,3'-Diaryl-BINOL phosphoric acids as enantioselective extractants of benzylic primary amines.

    Science.gov (United States)

    Verkuijl, Bastiaan J V; de Vries, Johannes G; Feringa, Ben L

    2011-01-01

    We report that 3,3'-diaryl-BINOL phosphoric acids are effective enantioselective extractants in chiral separation methods based on reactive liquid-liquid extraction. These new extractants are capable of separating racemic benzylic primary amine substrates. The effect of the nature of the substituents at the 3,3'-positions of the host were examined as well as the structure of the substrate, together with important parameters such as the organic solvent, the pH of the aqueous phase, and the host stoichiometry. Titration of the substrate with the host was monitored by FTIR, NMR, UV-Vis, and CD spectroscopy, which provided insight into the structure of the host-guest complex involved in extraction. Copyright © 2010 Wiley-Liss, Inc.

  12. Effect of Phosphoric Acid Concentration on the Optical Properties of Partially Phosphorylated PVA Complexes

    Directory of Open Access Journals (Sweden)

    Asmalina Mohamed Saat

    2014-01-01

    Full Text Available Partially phosphorylated polyvinyl alcohol (PPVA films were prepared at five mole ratios of phosphoric acid (PA using solution casting technique. The optical properties of the PPVA films were examined using UV-visible (UV and photoluminescence (PL spectroscopy. The UV absorption spectra reveal that the absorption peaks are blue-shifted with an increase in PA concentration added to the pure PVA. The PL spectra show the presence of peaks which are characteristic of isotactic (389–398, 460–462 nm, syndiotactic (418–420 nm, and atactic (440–446 nm configurations of the PPVA. The results also show the peak of O–P–O bonding at a wavelength range of 481–489 nm.

  13. The Results of HLW Processing Using Zirconium Salt of Dibutyl phosphoric Acid in Hot Cell

    Energy Technology Data Exchange (ETDEWEB)

    Fedorov, Yu.S.; Zilberman, B.Ya.; Shmidt, O.V. [Khlopin Radium Institute, 2nd Murinsky Ave., 28, Saint-Petersburg, 194021 (Russian Federation)

    2008-07-01

    Zirconium salt of dibutyl phosphoric acid (ZS HDBP), is an effective solvent for liquid HLW and ILW (high and intermediate level wastes) processing with radionuclide partitioning into different groups for further immobilization according to radiotoxicity. The rig trials in mixer-settles in hot cells were carried out using 30 L of real HLW containing transplutonium (TPE), rare earths (RE), Sr and Cs in 2 mol/L HNO{sub 3}, characterized by total specific activity 520 MBk/L. The recovery factor for TPE and RE was as high as 10{sup 4}, but only 10 for Sr. Purification factor of TPE and RE from Cs and Sr was 10{sup 4}, and that of Sr from TPE and Cs was 10{sup 3}. Almost all Cs was localized in the second cycle raffinate. So Zr salt of HDBP can be used in HLW processing with radionuclide partitioning with respect to the categories of radiotoxicity. (authors)

  14. Synthesis of the mono- and di(4-(1,1,3,3-tetramethylbutyl)) phosphoric acids

    International Nuclear Information System (INIS)

    Elias, H.; Zaoui, A.; Attou, M.; Hadj Bachir, D.; Bouzidi, N.; Didi, M.

    1995-09-01

    This work is related to the synthesis of organophosphorus extracting agents used in purification of heavy metals such as uranium. The mono- and di (4-(1,1,3,3- tetramethylbutyl)) phenyl phosphoric acids, respectively MOPPA and DOPPA, are synthesizd by reaction of phosphorus pentoxid with 4(1,1,3,3-tetramethylbuthyl)) phenol. the separation of MOPPA from DOPPA is realised by liquid-liquid extraction. The Characterization, carried out by infrared uv-visible spectrophotometries, ph-metry and mass spectrometry, has confirmed the identity of the synthesized products. This study also showed that the products proportions are comporable to those of the homologous products obtained with 2-ethylbexanol in the same synthesis conditions

  15. Performance Degradation Tests of Phosphoric Acid Doped PBI Membrane Based High Temperature PEM Fuel Cells

    DEFF Research Database (Denmark)

    Zhou, Fan; Araya, Samuel Simon; Grigoras, Ionela

    2014-01-01

    Degradation tests of two phosphoric acid (PA) doped PBI membrane based HT-PEM fuel cells were reported in this paper to investigate the effects of start/stop and the presence of methanol in the fuel to the performance degradation. Continuous tests with H2 and simulated reformate which was composed...... of H2, water steam and methanol as the fuel were performed on both single cells. 12-h-startup/12-h-shutdown dynamic tests were performed on the first single cell with pure dry H2 as the fuel and on the second single cell with simulated reformate as the fuel. Along with the tests electrochemical...... techniques such as polarization curves and electrochemical impedance spectroscopy (EIS) were employed to study the degradation mechanisms of the fuel cells. Both single cells showed an increase in the performance in the H2 continuous tests, because of a decrease in the ORR kinetic resistance probably due...

  16. Analysis and evaluation of the possibility of introducing phosphoric acid fuel cells

    Science.gov (United States)

    1991-03-01

    Each step in the manufacture of fuel cells is reviewed. The possibility of cost reduction in the process is investigated. Additionally, the feasibility of providing financial assistance for fuel cell buyers is investigated. Also, the present status and the future outlook of fuel cell development are discussed. In Japan, phosphoric acid fuel cells are beginning demonstration testing. A 200 kW test plant, for commercial and remote island use, has finished its demonstration test favorably. The test run of an 11 mW plant, for the production of electric power, is being conducted by a private company. The manufacture of each of the fuel cell's subsystems is semi-automated at this time. The costs are estimated to be reduced to 60 - 80 percent of the present costs in a 10 mW/year plant and TO 50 - 60 percent of the present costs in a 100 mW/year plant.

  17. Energetic and exergetic analysis of a steam turbine power plant in an existing phosphoric acid factory

    International Nuclear Information System (INIS)

    Hafdhi, Fathia; Khir, Tahar; Ben Yahyia, Ali; Ben Brahim, Ammar

    2015-01-01

    Highlights: • The operating mode of the factory and the power supply streams are presented. • Energetic Analysis of steam turbine power plant of an existing phosphoric acid factory. • Exergetic Analysis of each component of steam turbine power plant and the different heat recovery system. • Energy, exergy efficiency and irreversibility rates for the main components are determined. • The effect of the operating parameters on the plant performance are analyzed. - Abstract: An energetic and exergetic analysis is conducted on a Steam Turbine Power Plant of an existing Phosphoric Acid Factory. The heat recovery systems used in the different parts of the plant are also considered in the study. Mass, energy and exergy balances are established on the main compounds of the plant. A numerical code is established using EES software to perform the calculations required for the thermal and exergy plant analysis considering real variation ranges of the main operating parameters such as pressure, temperature and mass flow rate. The effects of theses parameters on the system performances are investigated. The main sources of irreversibility are the melters, followed by the heat exchangers, the steam turbine generator and the pumps. The maximum energy efficiency is obtained for the blower followed by the heat exchangers, the deaerator and the steam turbine generator. The exergy efficiency obtained for the heat exchanger, the steam turbine generator, the deaerator and the blower are 88%, 74%, 72% and 66% respectively. The effects of High Pressure steam temperature and pressure on the steam turbine generator energy and exergy efficiencies are investigated.

  18. Uranium(VI) and ruthenium extraction by dialkyldithio-phosphoric acids

    International Nuclear Information System (INIS)

    Fitoussi, R.; Musikas, C.

    1980-01-01

    Oxygen donors like dialkylphosphoric acids are good extractants for actinide ions, but little is known about their sulfur homologs. Investigations of U(VI) and Ru extraction from various aqueous media are reported. This includes extraction of U(VI) from nitric, perchloric, and phosphoric acids by solutions of dialkyldithiophosphoric acids in dodecane or benzene. Extraction of U(VI) by synergistic mixtures, of which at least one of the components is a sulfur donor, has been investigated. The extracted species have been identified, and a comparison with the complexes obtained by extraction with the homologous oxygen donors is made. The sulfur-actinide bond is weaker than the oxygen-actinide one, but in some synergistic extractions the dialkyldithiophosphonates are more efficient than the oxygen donors. In addition to size effects, this behavior could be attributed to the weakness of the hydrogen bonds of the SH groups, which allows a greater variety of the ligands to enter the coordination sphere of the metal. Ruthenium, like the d-transition elements, gives strong bonds with the sulfur donors. However, its extraction from nitric acid is slow. We investigated the influence of several parameters on the distribution coefficients and found that the presence of a reagent which destroys nitrous ions is necessary to achieve quantitative extraction. The role of RuNO groups is also discussed

  19. Liquid-liquid extraction for purification of wet process phosphoric acid

    International Nuclear Information System (INIS)

    Lotfollahi, Mohammad Nader; Bakshi, Mahdi

    2006-01-01

    The Wet Process Phosphoric Acid (WPA) is used to produce fertilizers and alimentary supplies for cattle. In each of these applications, the impurities contained in acid must be in standard range. In this paper purification of WPA by solvent extraction is performed and the effect of the mass ratio of solvent to feed on extraction efficiency is studied. The working solvents are Methyl Iso Butyl Ketone (MIBK), Iso Amyl Alcohol (IAA) and the mixture of them. The results show that the IAA is better than other solvents in extraction of WPA. This solvent can extract 82.2% of acid after two extraction stages but MIBK can extract only 73.5% of acid after three extraction stages. For all of these solvents, the Pb and Cd concentrations go down to trace. The experimental results show that the maximum separation of Mg with MIBK is 87.5% which occurs at the mass ratio of solvent to feed eual to 4. In the case of IAA solvent the percent is 91.7% and the ratio is 8

  20. Extraction of indium from sulphate solutions with D2EHPA solutions using static mixers

    International Nuclear Information System (INIS)

    Nacevski, N.; Poposka, F.; Nikov, B.

    1995-01-01

    The possible use of static mixers as a reactor for the extraction of indium from sulphate solutions was investigated. The experimental work was focused on ''Kenics'' type static mixers, since these were found simplest and cheapest among a variety of models, and yet yielded acceptable preliminary results with low pressure drop along the reactor. A series of experiments was carried out in a stirred continuous flow reactor to compare the results. It was found that under certain (different) conditions both reactors perform satisfactorily. The energy consumption of a static mixer is of the same order of magnitude as that of a stirred vessel. The most significant achievement of the experimental work is establishing that the residence time in a static mixer is about two orders of magnitude less than that in a stirred reactor. (orig.)

  1. Phosphoric acid distribution in the membrane electrode assembly of high temperature proton exchange membrane fuel cells

    International Nuclear Information System (INIS)

    Kwon, Kyungjung; Park, Jung Ock; Yoo, Duck Young; Yi, Jung S.

    2009-01-01

    The ionomer content in electrode is one of the most important parameters for the high performance of fuel cells. The high temperature PEMFC based on phosphoric acid (PA)-doped polymer membrane with unhumidified reactant gases has a difficulty in controlling the liquid state PA ionomer content in electrode. To evaluate the PA content in electrode, the three techniques of cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and acid-base titration (ABT) are carried out in situ or ex situ. The properties of membrane electrode assembly (MEA) such as electrochemical surface area (ESA), ohmic resistance, charge transfer resistance, double layer capacitance and the amount of PA in MEA components (anode, cathode and membrane) are extracted by each technique. Ex situ CV with the usage of dry gases has a limitation in assessing the reliable ESA of unhumidified PEMFC. While in situ EIS presents some informative values of resistance and capacitance for understanding the PA distribution in MEA, its sensitivity to the PA content in MEA components needs to be higher for detecting a subtle change in PA distribution. Ex situ ABT supplies a clear PA distribution in MEA at room temperature but does not seem to reflect the operating state well at high temperatures. However, it can be used as a detection tool for the loss of the initial acid content in membrane during a long-term MEA durability study.

  2. Physicochemical properties of carbons prepared from pecan shell by phosphoric acid activation.

    Science.gov (United States)

    Guo, Yanping; Rockstraw, David A

    2007-05-01

    Activated carbons were prepared from pecan shell by phosphoric acid activation. The pore structure and acidic surface groups of these carbons were characterized by nitrogen adsorption, Boehm titration and transmittance Fourier infrared spectroscopy (FTIR) techniques. The characterization results demonstrated that the development of pore structure was apparent at temperatures 250 degrees C, and reached 1130m(2)/g and 0.34cm(3)/g, respectively, at 500 degrees C. Impregnation ratio and soaking time at activation temperature also affected the pore development and pore size distribution of final carbon products. At an impregnation ratio of 1.5, activated carbon with BET surface area and micropore volume as high as 861m(2)/g and 0.289cm(3)/g was obtained at 400 degrees C. Microporous activated carbons were obtained in this study. Low impregnation ratio (less than 1.5) and activation temperature (less than 300 degrees C) are favorable to the formation of acidic surface functional groups, which consist of temperature-sensitive (unstable at high temperature) and temperature-insensitive (stable at high temperature) two parts. The disappearance of temperature-sensitive groups was significant at temperature 300 degrees C; while the temperature-insensitive groups are stable even at 500 degrees C. FTIR results showed that the temperature-insensitive part was mostly phosphorus-containing groups as well as some carbonyl-containing groups, while carbonyl-containing groups were the main contributor of temperature-sensitive part.

  3. Phosphoric acid distribution in the membrane electrode assembly of high temperature proton exchange membrane fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Kwon, Kyungjung [Fuel Cell Group, Energy Lab, SAIT, Samsung Electronics Co., Ltd., San 14-1, Nongseo-dong, Giheung-gu, Yongin-si, Gyeonggi-do, 446-712 (Korea, Republic of)], E-mail: kfromberk@gmail.com; Park, Jung Ock; Yoo, Duck Young; Yi, Jung S. [Fuel Cell Group, Energy Lab, SAIT, Samsung Electronics Co., Ltd., San 14-1, Nongseo-dong, Giheung-gu, Yongin-si, Gyeonggi-do, 446-712 (Korea, Republic of)

    2009-11-01

    The ionomer content in electrode is one of the most important parameters for the high performance of fuel cells. The high temperature PEMFC based on phosphoric acid (PA)-doped polymer membrane with unhumidified reactant gases has a difficulty in controlling the liquid state PA ionomer content in electrode. To evaluate the PA content in electrode, the three techniques of cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and acid-base titration (ABT) are carried out in situ or ex situ. The properties of membrane electrode assembly (MEA) such as electrochemical surface area (ESA), ohmic resistance, charge transfer resistance, double layer capacitance and the amount of PA in MEA components (anode, cathode and membrane) are extracted by each technique. Ex situ CV with the usage of dry gases has a limitation in assessing the reliable ESA of unhumidified PEMFC. While in situ EIS presents some informative values of resistance and capacitance for understanding the PA distribution in MEA, its sensitivity to the PA content in MEA components needs to be higher for detecting a subtle change in PA distribution. Ex situ ABT supplies a clear PA distribution in MEA at room temperature but does not seem to reflect the operating state well at high temperatures. However, it can be used as a detection tool for the loss of the initial acid content in membrane during a long-term MEA durability study.

  4. Search for a developed method for the determination of Fe2 and Fe3 in Syrian Phosphoric acid

    International Nuclear Information System (INIS)

    Elian, Nuzhat; Kalak, Issam

    1988-08-01

    Phosphoric acid is the most important precursor for uranium production in Syria. Uranium extraction from phosphoric acid depends on the chemical composition of the acid, and most important is the relation between the proportions of iron I I/iron I II, and uranium I V/uranium V I, this proportion plays a very important role in different steps of the extraction. For this purposes two methods for determination of Iron I I and Iron I II in Syrian wet phosphoric acid spectrophotometrically were studied. The first one used 1.10 phenanthroline as complex agent. Iron I I formed red complex with 1.10 phenonstholine in the range of pH between 4 and 6, for determination of total iron. Iron I II was reduced to Iron I I with hydroxylamine hydrochloride. The second method used sulfosalycilic acid, Iron I II formed a yellow complex with sulfosalycilic acid. Total iron was determined in ammonium medium, but Iron I II was determined in pH=1.5. The sensibility of the tow methods and stability of their complex have been studied in normal laboratory conditions. 45 refs., 4 figs. (author)

  5. Direct uranium extraction from dihydrate and hemi-dihydrate wet process phosphoric acids by liquid emulsion membrane

    International Nuclear Information System (INIS)

    El-Hazek, N.T.; El Sayed, M.S.

    2003-01-01

    A new liquid emulsion membrane (LEM) process for uranium extraction from either dihydrate 28-30% P 2 O 5 (DH) or hemi-dihydrate 42-45% P 2 O 5 (HDH) wet process phosphoric acid is proposed. In this process, the organic component of the LEM is composed of a synergistic mixture of 0.1M di-2-ethyl hexyl phosphoric acid (DEHPA) and 0.025M trioctyl phosphine oxide (TOPO) with 4% Span 80. The internal or the strip acid phase is composed of 0.5M citric acid. The prepared LEM was proved to be stable in 42-45% P 2 O 5 acid concentration range and can, therefore, be applied to the phosphoric acid produced by the hemi-dihydrate process. After breakdown of the loaded emulsion, the uranyl citrate in the internal strip phase is separated by adding methanol followed by its calcination to the orange oxide. Most of the reagents used are recycled. The proposed process is characterized by simplicity, practically closed operation cycle in addition to lower capital and operating costs. (author)

  6. Evaluation of Bio-phosphor and HumicAcid on Growth Parameters and Oil Content in Evening Primrose (Oenotherabiennis L.

    Directory of Open Access Journals (Sweden)

    Zeinab Aghakhani

    2017-12-01

    Full Text Available Introduction: Evening primrose (OenotherabiennisL. is a relatively new and valuable oilseed crop for temperate region. Its oilseed is important because of high levels of unsaturated fatty acids, especially gamma-linolenic acid. Seeds contain 20-30% oil which includes 70% linoleic acid (LA and 10% gamma linolenic acid (GLA. Oil content in O. biennis is a quantitative trait which controlled by many genes and similar to any other quantitative traits varies with environmental conditionssuch factors as age of seed and growth conditions. Evening primrose oil, especially gamma-linolenic acid, has many therapeutic properties, and it uses as cure for many diseases such as Diabetes, Eczema, inflammation, Cardiovascular, Cancer, Autoimmune diseases, Rheumatoid Arthritis, Depression. Studies on Medicinal Plants in nature and farmlands show that the use of sustainable agriculturae andnatural sources are two suitable methods for producing healthy plants.Additionally, the use of bio-fertilizers lead to maximum yield and quality in these plants. Azizi et al.(6 showed that interactions of vermicompost and plant density had significant effect on oil content, oil density and refractive index of evening primrose oil. The best treatments were also including 2 Kg/m2 of vermicompost,20 plants/ m2in terms of oil production,9 plants/ m2in terms of oil quality and ratio of unsaturated fatty acids to saturated, respectively. Material and Method: The aim of this research was to determine the effect of humic acid and bio-phosphor application on growth parameters in O. biennis. The experiment was conducted based on randomized complete block design with 8 treatments and three replicates during 2013-2014 growing season, at the experimental farm of the faculty of Agriculture, Ferdowsi University of Mashhad.. Treatments consisted of 4 levels of humic acid (0, 1, 3, 5 ml/L and 2 levels of bio-phosphor (without bio-phosphor or with bio-phosphor. Liquid form of humic acid was used

  7. Studies on the solvent extraction behaviour of Pu(IV) from nitric acid, nitric-perchloric acid and hydrochloric acids, by di,2-ethylhexyl phosphoric acid (HDEHP)

    International Nuclear Information System (INIS)

    Phal, D.G.; Kannan, S.K.; Ramakrishna, V.V.

    1994-01-01

    Extraction of plutonium (IV) from aqueous nitric acid, nitric-perchloric acid and hydrochloric acids by di,2-ethylhexyl phosphoric acid, the dimeric form of which is represented as H 2 Y 2 , in different diluents (dodecane, toluene and chloroform) was investigated. The composition of the extracted Pu(IV) species were found to be Pu(NO 3 ) 2 (HY) 2 , Pu(NO 3 )(ClO 4 )(HY 2 ) 2 , PuClY(HY 2 ) 2 and PuCl 2 (HY 2 ) 2 from nitric, nitric-perchloric and hydrochloric acids respectively, the last one being pre-dominant at high aqueous acidities (i.e. 5M HCl). Synergic enhancement in the extraction of Pu(IV) from different aqueous media, by the addition of thenoyltrifluoroacetone (HTTA) to HDEHP was also investigated and was attributed to the formation and extraction of the species PuX(TTA)(HY 2 ) 2 , and Pu(TTA) 2 (HY 2 ) 2 where X=Cl - or NO 3 - . The addition of the neutral extractant TOPO to H 2 Y 2 also resulted in synergism. The possible equilibria in these systems were inferred and the corresponding equilibrium constants determined. (author). 24 refs., 10 figs., 10 tabs

  8. Corrosion inhibition of austenitic stainless steel by clay in polluted phosphoric acid with presence of SiC abrasif

    Directory of Open Access Journals (Sweden)

    Skal S.

    2018-01-01

    Full Text Available Stainless steels have many properties mechanical and chemical resistances resulting from the formation of the protective layer (passive film on their surface which prevents the metal to react with corrosive environments such as, phosphoric acid. This acid contains various impurities, including agressive agents and solid particles of gypsum, increase the risk of corrosion damage depending on the type of stainless steel used. In addition, it has been show that abrasion-corrosion causes an acceleration electrochemical process leading to a decrease in the resistance of materials. This work is to find a solution through an ecological inhibitor. That why we have been studied the effect of crude clay on corrosion behavior of Alloy 31 in polluted phosphoric acid with abrasive by electrochemical impedance spectroscopy (EIS . The clay was characterized by X-ray fluorescence spectroscopy (FX, X-ray diffraction (DRX and infrared spectroscopy (IR. EIS exhibited that resistance of Alloy 31 increased with increase the concentration of inhibitor.

  9. Evaluation of human dental loss caused by carbamide peroxide bleacher compared with phosphoric acid conditioning - radioactive method

    International Nuclear Information System (INIS)

    Adachi, Eduardo Makoto; Yousseff, Michel Nicolau; Saiki, Mitiko

    2002-01-01

    The radiometric method was applied to the evaluation of dental loss caused by carbamide peroxide when it is applied on the surface layers of enamel and dentin tissues. Also the dental loss caused by the etching with 37% phosphoric acid procedure used in aesthetic restoration was assessed for comparison with those results obtained. The tooth samples irradiated with a P standard in a thermal neutron flux of the nuclear reactor were placed in contact with 10% carbamide peroxide or with 37% phosphoric acid solution. The radioactivity of 32 P transferred from the radioactive teeth to the bleaching gel or to etching acid was measured using a Geiger Muller detector to calculate the mass of P removed in this treatment and losses were calculated after obtaining their P concentrations. Results obtained indicated that enamel and dentin exposed to carbamide peroxide bleaching agent lose phosphorus. The extent of enamel loss was smaller than that obtained for dentin. In the case of acid etching, there was no difference between the results obtained for enamel and dentin loss. Also the dentin loss obtained after a treatment of 30 applications of 10% carbamide peroxide was the same magnitude of that one application of 37% phosphoric acid. (author)

  10. A Novel Method for Fabricating Double Layers Porous Anodic Alumina in Phosphoric/Oxalic Acid Solution and Oxalic Acid Solution

    Directory of Open Access Journals (Sweden)

    Yanfang Xu

    2016-01-01

    Full Text Available A novel method for fabricating ordered double layers porous anodic alumina (DL-PAA with controllable nanopore size was presented. Highly ordered large pore layer with interpore distance of 480 nm was fabricated in phosphoric acid solution with oxalic acid addition at the potential of 195 V and the small pore layer was fabricated in oxalic acid solution at the potential from 60 to 100 V. Experimental results show that the thickness of large pore layer is linearly correlative with anodizing time, and pore diameter is linearly correlative with pore widening time. When the anodizing potential in oxalic acid solution was adjusted from 60 to 100 V, the small pore layers with continuously tunable interpore distance from 142 to 241 nm and pore density from 1.94×109 to 4.89×109 cm−2 were obtained. And the interpore distance and the pore density of small pore layers are closely correlative with the anodizing potential. The fabricated DL-PAA templates can be widely utilized for fabrication of ordered nanomaterials, such as superhydrophobic or gecko-inspired adhesive materials and metal or semiconductor nanowires.

  11. Thermal properties of phosphoric acid-doped polybenzimidazole membranes in water and methanol-water mixtures

    Energy Technology Data Exchange (ETDEWEB)

    Nores-Pondal, Federico J.; Corti, Horacio R. [Grupo de Pilas de Combustible, Departamento de Fisica de la Materia Condensada, Centro Atomico Constituyentes, Comision Nacional de Energia Atomica (CNEA), Av. General Paz 1499, B1650KNA San Martin, Buenos Aires (Argentina); Consejo Nacional de Investigaciones Cientificas y Tecnicas (Argentina); Buera, M. Pilar [Consejo Nacional de Investigaciones Cientificas y Tecnicas (Argentina); Departamento de Industrias, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Av. Cantilo s/n, Ciudad Universitaria (1428) Buenos Aires (Argentina)

    2010-10-01

    The thermal properties of phosphoric acid-doped poly[2-2'-(m-phenylene)-5-5' bi-benzimidazole] (PBI) and poly[2,5-benzimidazole] (ABPBI) membranes, ionomeric materials with promising properties to be used as electrolytes in direct methanol and in high temperature polymer electrolyte membrane (PEM) fuel cells, were studied by means of differential scanning calorimetry (DSC) technique in the temperature range from -145 C to 200 C. The DSC scans of samples equilibrated in water at different relative humidities (RH) and in liquid water-methanol mixtures were analyzed in relation to glass transition, water crystallization/melting and solvent desorption in different temperature regions. The thermal relaxation observed in the very low temperature region could be ascribed to the glass transition of the H{sub 3}PO{sub 4}-H{sub 2}O mixture confined in the polymeric matrix. After cooling the samples up to -145 C, frozen water was detected in PBI and ABPBI at different RH, although at 100% RH less amount of water had crystallized than that observed in Nafion membranes under the same conditions. Even more important is the fact that the freezing degree of water is much lower in ABPBI membranes equilibrated in liquid water-methanol mixtures than that observed for PBI and, in a previous study, for Nafion. Thus, apart from other well known properties, acid-doped ABPBI emerges as an excellent ionomer for applications in direct methanol fuel cells working in cold environments. (author)

  12. Treatment alternatives of liquid radioactive waste containing uranium in phosphoric acid

    International Nuclear Information System (INIS)

    Bustamante Escobedo, Mauricio

    2003-01-01

    The UGDR, receives annually 100 [l] of liquid radioactive waste containing, highly acid (pH=0) uranium in phosphoric acid from the Laboratory of Chemical Analysis. This waste must be chemically and radiologically decontaminated before it can be discharged in accordance with local environmental standards. Chemical precipitation and evaporation test were carried out to define the operating conditions for the radiological decontamination of this radioactive waste and to obtain a solid waste that can be conditioned in a cement matrix. The evaporation process generates excellent rates of volume reduction, over 80%, but generates a pulp that is hard handle when submitted to a drying process. Chemical precipitation generates good results for decontaminating these solutions and reducing volume (above 50%) to obtain a uranium free effluent. The treatment with calcium carbonate generated an effluent with a low concentration of polluting agents. A preliminary test was carried out condition these solids in a cement matrix, using ratios of 0.45 waste/cement and 2 of water/cement. The mix prepared with waste from the sodium hydroxide treatment had low mechanical resistance resulting from the saline incrustations. The waste from the calcium carbonate treatment was very porous due to the water evaporation from the highly exothermic reaction between the waste and the cement. The mix of the calcium carbonate generated waste and the cement matrix needs to be optimized, since it generates favorable conditions for adhering with the cement matrix (au)

  13. Passivation behaviour of stainless steel (UNS N-08028) in industrial or simplified phosphoric acid solutions at different temperatures

    International Nuclear Information System (INIS)

    Ben Salah, M.; Sabot, R.; Refait, Ph.; Liascukiene, I.; Méthivier, C.; Landoulsi, J.; Dhouibi, L.

    2015-01-01

    Highlights: • Industrial phosphoric acid is less aggressive than simulated industrial acid. • Polyphosphate film in Industrial acid is reinforced by calcium and sulfate. • Passive film thickness is obtained by the power law model from EIS measurements. • Passive film of Sanicro28 becomes more resistive towards corrosion with exposure time in industrial acid. • XPS measurements coupled to Raman spectroscopy reveal the corrosion products formed in simulated acid. - Abstract: The corrosion behaviour of Sanicro28, in industrial phosphoric acid and simplified solution of pure H_3PO_4 containing sulphates and chlorides, is investigated during 48 h between 20 and 80 °C. Results show higher corrosion resistance in the industrial medium. Film thickness evaluated by EIS remains constant in industrial acid due to polyphosphate that promotes crystallisation of the Cr_2O_3 inner layer. Conversely, the passive film is partially destroyed at 80 °C in simplified acid. XPS and Raman analysis show that phosphate and molybdenum are both present in the passive film and in corrosion products. The role of Ca present in the industrial acid is discussed.

  14. Contribution to the study of dialcoylphosphates. The dibenzyl-phosphoric acid and its application to liquid-liquid extraction

    International Nuclear Information System (INIS)

    Courtemanche, Pierre V.

    1966-01-01

    This research thesis is a contribution to the knowledge of organophosphate compounds, and more particularly dialcoylphosphates, and even more particularly the dibenzyl-phosphoric acid or dibenzyl-phosphate (HDBzP). In a first part, the author reports studies on the synthesis of this compound by solving the specific analytic problem raised by simple organophosphates regarding their separation and identification. He also reports the study of some specific metallic derived compounds. The second part addresses the study of a specific feature of dialcoylphosphates: their interesting power of extraction with respect to metallic cations. The author shows that, through specific operational conditions (solvent nature, concentration of the extraction agent, composition of the aqueous phase containing the metallic ion), it is even possible to obtain a selective extraction. Thus, the author reports a physical-chemical study of the extraction agent, the dibenzyl-phosphoric acid

  15. The impact of water concentration on the catalytic oxidation of ethanol on platinum electrode in concentrated phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Camargo, A.P.M.; Previdello, B.A.F.; Varela, H.; Gonzalez, E.R. [Instituto de Quimica de Sao Carlos, Universidade de Sao Paulo, C.P. 780, CEP 13560-970 Sao Carlos, SP (Brazil)

    2010-01-15

    The electro-oxidation of ethanol on platinum in phosphoric acid opens the door to promote the oxidation reaction at higher temperatures. However, the effect of the presence of water is not well understood. In this work, the electro-oxidation of ethanol on platinum was studied in concentrated phosphoric acid containing different concentrations of water at room temperature. The results show that effect of bulk water on the rate electro-oxidation is highest at 0.60 V and decreases for increasing potentials. This was suggested as due to the increasing formation of oxygenated species on the electrode surface with potential, which in turn is more efficient than the increase of water content in the electrolyte. Altogether, these results were interpreted as an evidence of a Langmuir-Hinshelwood step involving oxygenated species as one of the adsorbed partners. (author)

  16. Laser enhanced reductions of uranium(VI) ion in aqueous phosphoric acid solutions

    International Nuclear Information System (INIS)

    Park, Y.Y.; Harada, M.; Tomiyasu, H.; Ikeda, Y.; Takashima, Y.

    1991-01-01

    Photochemical reactions of U(VI) ions with inorganic anions (I - , Br - , Cl - , NCS - ) and organic compounds (1-hexene, cyclohexene, pyridine) in phosphoric acid were studied for the purpose of finding an efficient method of adjusting the oxidation states of uranium ions in nuclear fuel reprocessing. The formation of U(IV) was observed in the photoreactions with I - , Br - and NCS - , but not with Cl - . The yield of U(VI) increased in the order, Br - - - . This order was the same as the quenching rate constants of the excited U(VI) ions with these anions, and the reverse of their standard redox potentials. The rates of the formation of U(IV) in the presence of Br - were measured spectrophotometrically. It was found that the rate equation was first order in both [U(VI)] and [Br - ]. The results were reasonably interpreted by a series of reaction processes involving U(V) and Br radical. With organic molecules, 1-hexene, cyclohexene, and pyridine, the formation of U(IV) were observed. The yield of U(IV) increased in the order pyridine < 1-hexene < cyclohexene. This order is the reverse of their vertical ionization potentials, suggesting an electron transfer mechanism between these organic molecules and excited U(VI). (author)

  17. Phosphoric acid pretreatment of Achyranthes aspera and Sida acuta weed biomass to improve enzymatic hydrolysis.

    Science.gov (United States)

    Siripong, Premjet; Duangporn, Premjet; Takata, Eri; Tsutsumi, Yuji

    2016-03-01

    Achyranthes aspera and Sida acuta, two types of weed biomass are abundant and waste in Thailand. We focus on them as novel feedstock for bio-ethanol production because they contain high-cellulose content (45.9% and 46.9%, respectively) and unutilized material. Phosphoric acid (70%, 75%, and 80%) was employed for the pretreatment to improve by enzymatic hydrolysis. The pretreatment process removed most of the xylan and a part of the lignin from the weeds, while most of the glucan remained. The cellulose conversion to glucose was greater for pretreated A. aspera (86.2 ± 0.3%) than that of the pretreated S. acuta (82.2 ± 1.1%). Thus, the removal of hemicellulose significantly affected the efficiency of the enzymatic hydrolysis. The scanning electron microscopy images showed the exposed fibrous cellulose on the cell wall surface, and this substantial change of the surface structure contributed to improving the enzyme accessibility. Copyright © 2015 Elsevier Ltd. All rights reserved.

  18. Energy efficient process for making pyrophyllite-based ceramic tiles using phosphoric acid and mineralizers

    Energy Technology Data Exchange (ETDEWEB)

    Amritphale, S.S.; Sanjeev Bhasin; Navin Chandra [Habib Ganj Naka, Pradesh (India). Regional Research Laboratory

    2006-07-01

    The processing parameters for making ceramic tiles in the pyrophyllite-phosphoric acid binder (P-PA) system have been optimized. The optimized raw material composition requires sintering at a lower temperature of 950{sup o}C. The X-ray powder diffraction studies on the powdered sample of optimized composition have confirmed the presence of dehydroxylate pyrophyllite, tridymite (T-AlPO{sub 4}), cristyoballite (C-AlPO{sub 4}) forms of aluminium phosphate and formation of silico-phosphate (SiP{sub 2}O{sub 7}) and alkali aluminium silicates (NaAlSiO{sub 4}, KAlSi{sub 3}O{sub 8}). The IR studies of the sample show Al-O, Si-O.P-O and Na/K-O linkages. The thermal analysis shows the formation of dehydroxylate pyrophyllite and different forms of AlPO{sub 4}. Scanning electron microphotograph reveals the chunky morphology of the dehydroxylate pyrophyllite, the rhombohedral morphology of T-AlPO{sub 4} and spherical C-AlPO{sub 4} and silico-phosphate particles. (author)

  19. Preparation and Characterization of Various Activated Carbons Derived From Mixed Precursors Using Phosphoric Acid

    International Nuclear Information System (INIS)

    Daifullah, A.A.M.; Sharaf El-Deen, S.E.A.; Elkhalafawy, A.; Shehata, F.A.; Mahmoud, W.H.

    2008-01-01

    Rice straw (RS) and rice husk (RH), a low-cost agricultural by-products, have been used as a mixed precursor (i.e., RS mixed with RH in 1:1; 1:3 and 3:1 ratios) for the production of novel carbons using phosphoric acid as chemical activation. The raw materials were impregnated with 50% and 70% H 3 PO 4 followed by activation at 500 degree C. The latter proved to be the most effective in producing active carbon with good adsorptive capacity. The resulting carbons were characterized by elemental analysis, infrared spectroscopy, density, SEM and S BET . In general, the resulting carbons showed reasonable surface areas with mainly micropore structure. The adsorption capacity was demonstrated by the isotherms of methylene blue (MB), phenol and iodine from aqueous solution. The adsorption data was found to conform with the Langmuir equation with the concentration range studied, and the monolayer coverage was determined for each of the samples. It was found that surface area is mainly attributed to micropore volume so that phenol adsorption and iodine number correspond well with surface area determined by nitrogen adsorption

  20. Study of oxidation-reduction reactions of plutonium and neptunium in sulphuric-phosphoric acid media

    International Nuclear Information System (INIS)

    Moiseev, I.V.; Kuperman, A.Ya.; Borodina, N.N.; Galkina, V.N.; Vinokurov, V.A.

    1976-01-01

    Potentiostatic, coulometric, potentiometric, and amperometric methods have been used for determining the rate constants of disproportionation (ksub(d)) of plutonium(5) and neptunium (5) and normal real redox potentials (Esub(0)sup(p)) of the following ion pairs in sulphur-phosphoric-acid media: PuOsub(2)sup(2)sup(+) (PuO 2 + , Pu 4+ /Pu 3+ , NpO 2 2+ /NpO 2 + , NpO 2 2+ /Np 4+ , NpO 2 + /Np 4+ , and Fe 3+ /Fe 2+ . The regularities have been shown of changing ksub(d) and Esub(o)sup(p) as a function of H 2 SO 4 and H 3 PO 4 concentration. It has been established that for plutonium and neptunium a linear correlation is observed between lg ksub(d) and Esub(o)sup(p) of the ion pairs NpO 2 2+ /NpO 2 + , NpO 2 2 /Np 4+ , NpO 2 + /Np 4+ and PuO 2 2+ /PuO 2 + in a wide range of their values. The correlation coefficient is close to unity in all cases (no less than 0.96). The results of investigations have made it possible to recommend optimum compositions of background electrolytes for performing continuous amperostatic coulometric titration of Pusup((6)) and Npsup((6)) up to four valent state by electrogenerated ions of iron (2)

  1. New Trident Molecule with Phosphoric Acid Functionality for Trivalent Rare Earth Extraction

    Directory of Open Access Journals (Sweden)

    Keisuke Ohto

    2017-11-01

    Full Text Available Tripodal extraction reagent with three phosphoric acid groups, together with the corresponding monopodal molecule has been prepared to investigate some metals extraction behavior, in particular, trivalent rare earth elements (REEs. The tripodal reagent exhibited extremely high selectivity for metals with high valency such as Zr(IV, In(III, Lu(III, and Fe(III. Tripodal reagent also exhibited exceptionally high extraction ability compared with the corresponding monopodal one in the extraction of trivalent rare earths. The result for the stoichiometry of tripodal reagent to heavy rare earths showed the inflection point between Er (2:1 for a ligand with ion and Tm (1:1. The extraction reactions were determined for all rare earths with both reagents. The extraction equilibrium constants (Kex, the separation factors (β, half pH values (pH1/2, difference half pH values (ΔpH1/2 for extraction of REEs with both reagents are estimated.

  2. Effect of aluminum anodizing in phosphoric acid electrolyte on adhesion strength and thermal performance

    Science.gov (United States)

    Lee, Sulki; Kim, Donghyun; Kim, Yonghwan; Jung, Uoochang; Chung, Wonsub

    2016-01-01

    This study examined the adhesive bond strength and thermal performance of the anodized aluminum 6061 in phosphoric acid electrolyte to improve the adhesive bond strength and thermal performance for use in metal core printed circuit boards (MCPCB). The electrolyte temperature and applied voltage were altered to generate varied pore structures. The thickness, porosity and pore diameter of the anodized layer were measured. The pore morphologies were affected most by temperature, which was the driving force for ion transportation. The mechanism of adhesive bond was penetration of the epoxy into the pores. The optimal anodization conditions for maximum adhesive bond strength, 27 MPa, were 293 K and 100V. The maximum thermal conductivity of the epoxy-treated anodized layer was 1.6 W/m·K at 273 K. Compared with the epoxy-treated Al layer used for conventional MCPCBs, the epoxy-treated anodized layer showed advanced thermal performance due to a low difference of thermal resistance and high heat dissipation.

  3. Phosphoric acid activation of sugarcane bagasse for removal of o-toluidine and benzidine

    Science.gov (United States)

    Adib, M. R. M.; Attahirah, M. H. M. N.; Amirza, A. R. M.

    2018-04-01

    In the effort to find alternatives for low cost adsorbent, activated carbon using sugarcane bagasse (SBAC) has been introduced in this study that has undergo chemical treatment using phosphoric acid to determine the effectiveness of adsorption process in removing o-toluidine and benzidine. Throughout this study, 92.9% of o-toluidine has been successfully removed by SBAC at optimum value of 1.1 g of dosage with contact time of 10 minutes and concentration of 10 mg/L. While benzidine was remove by 83.1% at optimum dosage of 1.1 g with 60 minutes of contact time and at 20 mg/L concentrations. Testing of SEM proves that SBAC has high porosity and comparable to CAC. In FTIR results, shows that CAC has high number of double bond while SBAC shows no double bond at all. Presence of double bond in CAC lead to increase in percentage of removal of adsorbate. After considering other factor such as cost, energy and environmental friendly, it shows that SBAC was considerable to replaced CAC.

  4. Design of mixer settler extraction cycles II for recovery uranium from phosphoric acid

    International Nuclear Information System (INIS)

    Abdul Jami; Hafni Lissa Nuri

    2013-01-01

    Mixer settler is technically designed for extraction and separation process of uranium from phosphoric acid solution. Design calculation results shows that: the mixer settler consists of two parts: part of extraction process in the mixer tank and part of separation process in settler tank. The mixer tank type of box with 4 baffles, the size of mixer tank, 0.8 m width, 0.8 m length, 1 m high of liquid, 1.05 m high of mixer tank, stirrer type of disk 6 blade, and power of mixing 4 hp and the settler tank type of rectangular with size of settler tank, 0.8 m width 5 m length, 1 m high of liquid, 1.05 m high of settler tank. For uranium recovery efficiency up to 91%, extraction process is done in 3 stage counter current flow using a solvent Organic (O) DEHPA-TOPO in Kerosene at a phase of ratio A/O of 2:1. The aqueous enter through stage 3 and the organic solvent enter through stage 1. The process of settling occurred with the value of settling velocity is 0.000694 m/s, dispersion factor Ψ = 0.3638 and the light fraction as the dispersed phase and value of Reynolds number (NRE) = 3,438. Because of the Reynolds number is lower than 5,000, it indicates that the quality of the separation is very good. (author)

  5. Potential radiological impacts of recovery of uranium from wet-process phosphoric acid. Final report to the Environmental Protection Agency

    International Nuclear Information System (INIS)

    Davis, W. Jr.; Haywood, F.F.; Danek, J.L.; Moore, R.E.; Wagner, E.B.; Rupp, E.M.

    1979-01-01

    A study was made to determine the radiological impacts associated with recovery of uranium from wet-process (WP) phosphoric acid in central Florida. Removal of U and other radionuclides from phosphoric acid prevents their distribution on farm lands and urban gardens and grasses via fertilizers; this results in a positive impact (decreased dose commitment) on the associated populations. This study considers the potential negative impacts of current and project recovery processes in a site-specific manner using detailed state-of-the-art methodologies. Positive impacts are treated in a generic sense using U.S. average values for important variables such as average and maximum fertilizer application rates and quantities of radionuclides in fertilizer. Three model plants to recover U from WP phosphoric acid were selected and source terms for release of radionuclides are developed for all three and for two treatment methods for airborne particulates. Costs for radwaste treatment were developed. Field measurements were conducted at the only commercial uranium recovery plant in operation. Radiological doses to the population surrounding release points during plant operation were estimated

  6. Electrolytes for methanol-air fuel cells. I. The performance of methanol electro-oxidation catalysts in sulphuric acid and phosphoric acid electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Andrew, M.R.; McNicol, B.D.; Short, R.T.; Drury, J.S.

    1977-03-01

    Phosphoric acid and sulphuric acid have been compared as potential electrolytes for methanol-air fuel cells. The performances of typical electro-oxidation catalysts were measured in both electrolytes over a range of concentrations. With all catalysts the activity falls with increasing acid concentration. While this is to some extent due to the decrease in water activity at higher concentrations it seems that with both acids there is significant poisoning of the catalyst. The results can be explained for both electrolytes by assuming that adsorption of undissociated acid poisons the catalyst surfaces and that the reaction rate on the poisoned surfaces is proportional to the water activity.

  7. Comparison of enamel bond fatigue durability between universal adhesives and two-step self-etch adhesives: Effect of phosphoric acid pre-etching.

    Science.gov (United States)

    Suda, Shunichi; Tsujimoto, Akimasa; Barkmeier, Wayne W; Nojiri, Kie; Nagura, Yuko; Takamizawa, Toshiki; Latta, Mark A; Miyazaki, Masashi

    2018-03-30

    The effect of phosphoric acid pre-etching on enamel bond fatigue durability of universal adhesives and two-step self-etch adhesives was investigated. Four universal adhesives and three two-step self-etch adhesives were used. The initial shear bond strengths and shear fatigue strengths to enamel with and without phosphoric acid pre-etching using the adhesives were determined. SEM observations were also conducted. Phosphoric acid pre-etching of enamel was found to increase the bond fatigue durability of universal adhesives, but its effect on two-step self-etch adhesives was material-dependent. In addition, some universal adhesives with phosphoric acid pre-etching showed similar bond fatigue durability to the two-step self-etch adhesives, although the bond fatigue durability of universal adhesives in self-etch mode was lower than that of the two-step self-etch adhesives. Phosphoric acid pre-etching enhances enamel bond fatigue durability of universal adhesives, but the effect of phosphoric acid pre-etching on the bond fatigue durability of two-step self-etch adhesives was material-dependent.

  8. Synergic extraction of some lanthanide and actinide elements by a mixture of bis(2-ethyl hexyl) phosphoric acid and dinonylnapthalene - sulfonic acid in aromatic diluents

    International Nuclear Information System (INIS)

    Raieh, M.A.; El-Dessouky, M.M.

    1985-01-01

    Extraction of lanthanides and actinides were found to be synergetically enhanced by a mixture of bis(2-ethyl hexyl) phosphoric acid (HA) and dinonylnaphthalene sulfonic acid (HD) in aromatic diluents covering a wide range of dielectric constants. The main extracted species is found to be MAsub(2)Hsub(m-1)Dsub(m). Experimental results indicate that the extraxtion mechanism is governed by the extraction of HD in the organic phase. (author)

  9. Study of the properties of dialkyl thiophosphoric acids. Application to the extraction of U, in phosphoric and nitric solutions

    International Nuclear Information System (INIS)

    Benjelloun, N.

    1983-09-01

    A study is made of complex formation and liquid-liquid extraction of uranium (VI) by dialkyl-thiophosphoric acids of formula (RO) 2 POSH 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 UO 2 2+ ions although U(VI) is considered as a ''hard class a'' acceptor according to Ahrland's classification [fr

  10. Influence of multi-step washing using Na2EDTA, oxalic acid and phosphoric acid on metal fractionation and spectroscopy characteristics from contaminated soil.

    Science.gov (United States)

    Wei, Meng; Chen, Jiajun

    2016-11-01

    A multi-step soil washing test using a typical chelating agent (Na 2 EDTA), organic acid (oxalic acid), and inorganic weak acid (phosphoric acid) was conducted to remediate soil contaminated with heavy metals near an arsenic mining area. The aim of the test was to improve the heavy metal removal efficiency and investigate its influence on metal fractionation and the spectroscopy characteristics of contaminated soil. The results indicated that the orders of the multi-step washing were critical for the removal efficiencies of the metal fractions, bioavailability, and potential mobility due to the different dissolution levels of mineral fractions and the inter-transformation of metal fractions by XRD and FT-IR spectral analyses. The optimal soil washing options were identified as the Na 2 EDTA-phosphoric-oxalic acid (EPO) and phosphoric-oxalic acid-Na 2 EDTA (POE) sequences because of their high removal efficiencies (approximately 45 % for arsenic and 88 % for cadmium) and the minimal harmful effects that were determined by the mobility and bioavailability of the remaining heavy metals based on the metal stability (I R ) and modified redistribution index ([Formula: see text]).

  11. PEM steam electrolysis at 130 °C using a phosphoric acid doped short side chain PFSA membrane

    DEFF Research Database (Denmark)

    Hansen, Martin Kalmar; Aili, David; Christensen, Erik

    2012-01-01

    Steam electrolysis test with a phosphoric acid doped Aquivion™ membrane was successfully conducted and current densities up to 775 mA cm-2 at 1.8 V was reached at 130 ºC and ambient pressure. A new composite membrane system using a perfluorosulfonic acid membrane (Aquivion™) as matrix and phospho...... implied that a new and highly corrosion resistant construction material was needed. Tantalum coated stainless steel felt was tested and found suitable as the anode gas diffusion layer. Copyright © 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved....

  12. Oxygen Reduction on Gas-Diffusion Electrodes for Phosphoric Acid Fuel Cells by a Potential Decay Method

    DEFF Research Database (Denmark)

    Li, Qingfeng; Gang, Xiao; Hjuler, Hans Aage

    1995-01-01

    The reduction of gaseous oxygen on carbon supported platinum electrodes has been studied at 150 degrees C with polarization and potential decay measurements. The electrolyte was either 100 weight percent phosphoric acid or that acid with a fluorinated additive, potassium perfluorohexanesulfonate ......6F13SO3K). The pseudo-Tafel curves of the overpotential vs. log (ii(L)/(i(L) - i)) show a two-slope behavior, probably due to different adsorption mechanisms. The potential relaxations as functions of log (t + tau) and log (-d eta/dt) have been plotted. The variations of these slopes...

  13. (Di­methyl­phosphor­yl)methanaminium hydrogen oxalate–oxalic acid (2/1)

    OpenAIRE

    Bialek, Sebastian; Clemens, Rebecca; Reiss, Guido J.

    2014-01-01

    The reaction of (di­methyl­phosphor­yl)methanamine (dpma) with oxalic acid in ethanol yielded the title solvated salt, C3H11NOP+·C2HO4 −·0.5C2H2O4. Its asymmetric unit consists of one dpmaH+ cation, one hydrogen oxalate anion and a half-mol­ecule of oxalic acid located around a twofold rotation axis. The H atom of the hydrogen oxalate anion is statistically disordered over two positions that are trans to each other. The hydrogen oxalate monoanion is not planar (bend angle ∼16°) whereas the ox...

  14. Recovery of fluorine, uranium, and rare earth metal values from phosphoric acid by-product brine raffinate

    International Nuclear Information System (INIS)

    Wamser, C.A.; Bruen, C.P.

    1976-01-01

    A method for recovering substantially all of the fluorine and uranium values and at least 90 percent of the rare earth metal values from brine raffinate obtained as by-product in the production of phosphoric acid by the hydrochloric acid decomposition of tricalcium phosphate minerals is described. A basically reacting compound is added to the brine raffinate to effect a pH 9 or greater, whereby fluorine, uranium and rare earth metal values are simultaneously precipitated. These values may then be separately recovered from the precipitate by known processes

  15. Contribution of native phosphorous-solubilizing bacteria of acid soils on phosphorous acquisition in peanut (Arachis hypogaea L.).

    Science.gov (United States)

    Pradhan, Madhusmita; Sahoo, Ranjan Kumar; Pradhan, Chinmay; Tuteja, Narendra; Mohanty, Santanu

    2017-11-01

    The present investigation analyzes the in vitro P solubilization [Ca-P, Al-P, Fe(II)-P, and Fe(III)-P] efficiency of native PSB strains from acid soils of Odisha and exploitation of the same through biofertilization in peanut (Arachis hypogaea L.) growth and P acquisition. One hundred six numbers of soil samples with pH ≤ 5.50 were collected from five districts of Odisha viz., Balasore, Cuttack, Khordha, Keonjhar, and Mayurbhanj. One bacterial isolate from each district were selected and analyzed for their P solubilization efficiency in National Botanical Research Institute Phosphate broths with Ca, Al, and Fe-complexed phosphates. CTC12 and KHD08 transformed more amount of soluble P from Ca-P (CTC12 393.30 mg/L; KHD08 465.25 mg/L), Al-P (CTC12 40.00 mg/L; KHD08 34.50 mg/L), Fe(III)-P (CTC12 175.50 mg/L; KHD08 168.75 mg/L), and Fe(II)-P (CTC12 47.40 mg/L; KHD08 42.00 mg/L) after 8 days of incubation. The bioconversion of P by all the five strains in the broth medium followed the order Ca-P > Fe(III)-P > Fe(II)-P > Al-P. The identified five strains were Bacillus cereus BLS18 (KT582541), Bacillus amyloliquefaciens CTC12 (KT633845), Burkholderia cepacia KHD08 (KT717633), B. cepacia KJR03 (KT717634), and B. cepacia K1 (KM030037) and further studied for biofertilization effects on peanut. CTC12 and KHD08 enhanced the soil available P around 65 and 58% and reduced the amount of each Al 3+ about 79 and 81%, respectively, over the uninoculated control pots in the peanut rhizosphere. Moreover, all tested PSB strains could be able to successfully mobilize P from inorganic P fractions (non-occluded Al-P and Fe-P). The strains CTC12 and KHD08 increased the pod yield (114 and 113%), shoot P (92 and 94%), and kernel P (100 and 101%), respectively, over the control. However, B. amyloliquefaciens CTC12 and B. cepacia KHD08 proved to be the potent P solubilizers in promoting peanut growth and yield.

  16. Spectrophotometric and potentiometric studies of oxidation of Mo(III) by Mo(VI) in phosphoric acid medium

    International Nuclear Information System (INIS)

    Kumar, Arvind; Verma, G.S.P.

    1975-01-01

    Oxidation of Mo(III) (green) by Mo(VI) in an inert atmosphere and in orthophosphoric acid medium at various acid concentrations is reported. Potentiometric and spectrophotometric data suggest that oxidation of Mo(III) proceeds to Mo(V) through a binuclear species Mo(III) Mo(IV) absorbing at 400 nm. The formation of this species is facilitated at high acid concentrations. It is further found that quantitative conversion of Mo(III) into Mo(V) takes place at fairly high acid concentrations. In high phosphoric acid concentrations, solution of Mo(III) has been found to be oxidized to Mo(VI) by air and hence this can be used as a good oxygen absorber. (author)

  17. Spectrophotometric and potentiometric studies of oxidation of Mo(III) by Mo(VI) in phosphoric acid medium

    Energy Technology Data Exchange (ETDEWEB)

    Kumar, A; Verma, G S.P. [Ranchi Coll. (India). Dept. of Chemistry

    1975-12-01

    Oxidation of Mo(III) (green) by Mo(VI) in an inert atmosphere and in orthophosphoric acid medium at various acid concentrations is reported. Potentiometric and spectrophotometric data suggest that oxidation of Mo(III) proceeds to Mo(V) through a binuclear species Mo(III) Mo(IV) absorbing at 400 nm. The formation of this species is facilitated at high acid concentrations. It is further found that quantitative conversion of Mo(III) into Mo(V) takes place at fairly high acid concentrations. In high phosphoric acid concentrations, solution of Mo(III) has been found to be oxidized to Mo(VI) by air and hence this can be used as a good oxygen absorber.

  18. 1000kW phosphoric acid fuel cell power plant. Outline of the plant

    Energy Technology Data Exchange (ETDEWEB)

    Shinobe, Kenji; Suzuki, Kazuo; Kaneko, Hideo

    1988-02-10

    The outline of the 1000KW phosphoric acid fuel cell power plant, developed as part of the Moonlight plan, was described. The plant was composed of 4 stacks of 260KW DC output. They were devided into two train with 680V and 765A. The generation efficiency of the plant was 40% and more. Steam reforming of natural gas was used. As the fuel, fuel cell exhaust gas was used in composition with the natural gas. The DC-AC inverter had an efficiency of 96%. The capacity of hot water generator and demineralized water plant for cell cooling were 2t/h and 1.6t/h, respectively, and air-system was incorporated. In September of 1987, the plant has succeeded in 1000KW power generation, and put in operation now. Under the 100% loaded condition, each cell had a voltage of 0.7V with little variation, and the current was 200mA/cm/sup 2/. No problems were found in cooling conditions and in the control of interpole differential pressure. The reformer has been operated for 1200h scince its commisioning, and had experiences of 100 times on start up-shut down operations, the reformer also indicated good performances in the gas compositions. The starting time of 8h and the load follow-up rate 10%/min remain as the subjects for shortening. DC-AC conversion was good. The concentration of NOx and the noise level satisfied the target values. (12 figs, 1 tab)

  19. Effect of Phosphoric Acid Concentration on the Characteristics of Sugarcane Bagasse Activated Carbon

    Science.gov (United States)

    Adib, M. R. M.; Suraya, W. M. S. W.; Rafidah, H.; Amirza, A. R. M.; Attahirah, M. H. M. N.; Hani, M. S. N. Q.; Adnan, M. S.

    2016-07-01

    Impregnation method is one of the crucial steps involved in producing activated carbon using chemical activation process. Chemicals employed in this step is effective at decomposing the structure of material and forming micropores that helps in adsorption of contaminants. This paper explains thorough procedures that have been involved in producing sugarcane bagasse activated carbon (SBAC) by using 5%, 10%, 20%, 30% phosphoric acid (H3PO4) during the impregnation step. Concentration of H3PO4 used in the process of producing SBAC was optimized through several tests including bulk density, ash content, iodine adsorption and pore size diameter and the charactesristic of optimum SBAC produced has been compared with commercial activated carbon (CAC). Batch study has been carried out by using the SBAC produced from optimum condition to investigate the performance of SBAC in removal of turbidity and chemical oxygen demand (COD) from textile wastewater. From characteristic study, SBAC with 30% H3PO4 has shown the optimum value of bulk density, ash content, iodine adsorption and pore size diameter of 0.3023 g cm-3, 4.35%, 974.96 mg/g and 0.21-0.41 µm, respectively. These values are comparable to the characteristics of CAC. Experimental result from the batch study has been concluded that the SBAC has a promising potential in removing turbidity and COD of 75.5% and 66.3%, respectively which was a slightly lower than CAC which were able to remove 82.8% of turbidity and 70% of COD. As a conclusion, the SBAC is comparable with CAC in terms of their characteristics and the capability of removing contaminants from textile wastewater. Therefore, it has a commercial value to be used as an alternative of low-cost material in producing CAC.

  20. Studies on the interference of hydrofluoric acid and phosphoric acid in the determination of uranium using Ti(III) reduction method-biamperometry end point

    International Nuclear Information System (INIS)

    Shiny, T.S.; Rajalakshmi, A.; Phal, D.G.; Charyulu, M.M.; Ramakumar, K.L.

    2007-01-01

    Accurate and precise determination of uranium in nuclear materials is necessary for chemical quality control as well as for nuclear material accounting purposes. Different types of uranium samples are received for the measurements. Depending upon the nature of the sample dissolution procedure is selected. Mixed oxide samples of uranium and plutonium, for example, are dissolved in nitric acid containing hydrofluoric acid under IR lamp. The fluoride ions are removed by repeated evaporation of the solution. However, some fluoride ions are left in the solutions depending on the conditions of evaporation. Uranium samples and alloy samples are dissolved in dilute hydrochloric acid. The rate of dissolution depends on concentration of acid. Sometimes a mixture of hydrochloric acid and hydrofluoric acid is used for the dissolution metal alloy samples, which may contain silica. Another method of dissolution of these samples is using a mixture of phosphoric acid and 1% hydrofluoric acid. It is necessary to study the interference of hydrofluoric acid and phosphoric acid on the determination of uranium

  1. Synthesis and characterization of new biopolymeric microcapsules containing DEHPA-TOPO extractants for separation of uranium from phosphoric acid solutions.

    Science.gov (United States)

    Outokesh, Mohammad; Tayyebi, Ahmad; Khanchi, Alireza; Grayeli, Fatemeh; Bagheri, Ghodrat

    2011-01-01

    A novel microcapsule adsorbent for separation of uranium from phosphoric acid solutions was developed by immobilizing the di(2-ethylhexyl) phosphoric acid-trioctyl phosphine oxide extractants in the polymeric matrix of calcium alginate. Physical characterization of the microcapsules was accomplished by scanning electron microscopy and thermogravimetric techniques. Equilibrium experiments revealed that both ion exchange and solvent extraction mechanisms were involved in the adsorption of [Formula: see text] ions, but the latter prevailed in a wider range of acid concentration. According to the results of kinetics study, at low acidity level, the rate controlling step was slow chemical reaction of [Formula: see text] ions with the microdroplets of extractant, whereas it changed to intraparticle diffusion at higher acid concentration. The study also attempted identification of the diffusion paths of the ions within the microcapsules, and the mechanism of change of mass transfer rate during the uptake process. The prepared microcapsules preserved their entire capacity after three cycles of adsorption, and their breakthrough behaviour was well fitted by a new formula derived from shrinking core model.

  2. Systematically controlled pore system of ordered mesoporous carbons using phosphoric acid as the in situ generated catalysts for carbonization and activation

    Energy Technology Data Exchange (ETDEWEB)

    Jin, Xing; Lee, Chang Hyun; Kim, Jin Hoe; You, Dae Jong; Shon, Jeong Kuk; Kim, Ji Man [Dept. of Chemistry, Sungkyunkwan University, Suwon (Korea, Republic of); Pak, Chan Ho [Fuel Cell Group, Corporate R and D Center, Samsung SDI Co. Ltd., Yongin (Korea, Republic of)

    2015-08-15

    We report on a facile synthesis of the ordered mesoporous carbon (OMC) materials with systematically controlled microporosity and mesoporosity simultaneously through the nano-replication route using phosphoric acid as the acid catalyst and activation agent. The use of phosphoric acid affects the pore structures of OMC materials, such as the formation of numerous micropores by activation of the carbon framework and the enlargement of mesopores by spontaneous phase separation during the carbonization. The mesopore sizes, surface areas, total pore volumes, and micropore volumes of the OMC materials are highly dependent on the phosphoric acid content and can be systematically controlled in the range 3.7–7.5 nm, 1027–2782 m{sup 2} g{sup -1}, 1.12–3.53 cm{sup 3} g{sup -1} and 0.34–0.95 cm{sup 3} g{sup -1}, respectively. OMC materials with systematically controlled pore structures were successfully synthesized using phosphoric acid as the carbonization catalyst and mesoporous silica materials with cubic Ia3d and 2-D hexagonal mesostructures as the templates. The phosphoric acid in the synthesis of ordered mesoporous carbon materials acts as the chemical activating agent for micropore generation of the carbon framework and pore-expanding agent for controlling of mesopore size, in addition to functioning as the acid catalyst. The present synthesis pathway is very useful for preparing OMC materials with tunable mesopore sizes and well-developed microporosities at the same time.

  3. The Effect of Phosphoric Acid Pre-etching Times on Bonding Performance and Surface Free Energy with Single-step Self-etch Adhesives.

    Science.gov (United States)

    Tsujimoto, A; Barkmeier, W W; Takamizawa, T; Latta, M A; Miyazaki, M

    2016-01-01

    The purpose of this study was to evaluate the effect of phosphoric acid pre-etching times on shear bond strength (SBS) and surface free energy (SFE) with single-step self-etch adhesives. The three single-step self-etch adhesives used were: 1) Scotchbond Universal Adhesive (3M ESPE), 2) Clearfil tri-S Bond (Kuraray Noritake Dental), and 3) G-Bond Plus (GC). Two no pre-etching groups, 1) untreated enamel and 2) enamel surfaces after ultrasonic cleaning with distilled water for 30 seconds to remove the smear layer, were prepared. There were four pre-etching groups: 1) enamel surfaces were pre-etched with phosphoric acid (Etchant, 3M ESPE) for 3 seconds, 2) enamel surfaces were pre-etched for 5 seconds, 3) enamel surfaces were pre-etched for 10 seconds, and 4) enamel surfaces were pre-etched for 15 seconds. Resin composite was bonded to the treated enamel surface to determine SBS. The SFEs of treated enamel surfaces were determined by measuring the contact angles of three test liquids. Scanning electron microscopy was used to examine the enamel surfaces and enamel-adhesive interface. The specimens with phosphoric acid pre-etching showed significantly higher SBS and SFEs than the specimens without phosphoric acid pre-etching regardless of the adhesive system used. SBS and SFEs did not increase for phosphoric acid pre-etching times over 3 seconds. There were no significant differences in SBS and SFEs between the specimens with and without a smear layer. The data suggest that phosphoric acid pre-etching of ground enamel improves the bonding performance of single-step self-etch adhesives, but these bonding properties do not increase for phosphoric acid pre-etching times over 3 seconds.

  4. The linear rule of metal extraction

    International Nuclear Information System (INIS)

    Han Li; Yushuang Wang; Zhichun Chen; Shulan Meng

    1988-01-01

    On the basis of experimental results a linear rule for the solvent extraction of rare earths and yttrium over a definite range of acidity and metal ion concentration is found. Relations between the coefficients of the linear rule and initial acidity are presented for the extraction systems: HEH(EHP)-kerosene-HNO 3 -R(NO 3 ) 3 , HEH(EHP)-kerosene-HCl-RCl 3 , D2EHPA-n-heptane-HCl-RCl 3 , HEH(EHP)-n-heptane-HCl-RCl 3 , where R=La-Nd, Sm-Lu, Y; HEH(EHP)=momo(2-ethyl-hexyl)2-ethyl-hexyl phosphonate; D2EHPA=di(2-ethyl-hexyl) phosphoric acid. 3 refs.; 1 tab

  5. Solubility Limits of Dibutyl Phosphoric Acid in Uranium Solutions at SRS

    International Nuclear Information System (INIS)

    Thompson, M.C.; Pierce, R.A.; Ray, R.J.

    1998-06-01

    The Savannah River Site has enriched uranium (EU) solution which has been stored for almost 10 years since being purified in the second uranium cycle of the H area solvent extraction process. The concentrations in solution are 6 g/L U and about 0.1 M nitric acid. Residual tributylphosphate in the solutions has slowly hydrolyzed to form dibutyl phosphoric acid (HDBP) at concentrations averaging 50 mg/L. Uranium is known to form compounds with DBP which have limited solubility. The potential to form uranium-DBP solids raises a nuclear criticality safety issue. SRTC tests have shown that U-DBP solids will precipitate at concentrations potentially attainable during storage of enriched uranium solutions. Evaporation of the existing EUS solution without additional acidification could result in the precipitation of U-DBP solids if DBP concentration in the resulting solution exceeds 110 ppm at ambient temperature. The same potential exists for evaporation of unwashed 1CU solutions. The most important variables of interest for present plant operations are HNO 3 and DBP concentrations. Temperature is also an important variable controlling precipitation. The data obtained in these tests can be used to set operating and safety limits for the plant. It is recommended that the data for 0 degrees C with 0.5 M HNO 3 be used for setting the limits. The limit would be 80 mg/L which is 3 standard deviations below the average of 86 observed in the tests. The data shows that super-saturation can occur when the DBP concentration is as much as 50 percent above the solubility limit. However, super-saturation cannot be relied on for maintaining nuclear criticality safety. The analytical method for determining DBP concentration in U solutions was improved so that analyses for a solution are accurate to within 10 percent. However, the overall uncertainty of results for periodic samples of the existing EUS solutions was only reduced slightly. Thus, sampling appears to be the largest portion

  6. Synthesis of Fluorite (CaF2 Crystal from Gypsum Waste of Phosphoric Acid Factory in Silica Gel

    Directory of Open Access Journals (Sweden)

    Mohammad Misbah Khunur

    2012-06-01

    Full Text Available This paper report the synthesis and characterization of fluorite single crystal prepared from gypsum waste of phosphoric acid production in silica gel. Instead of its high calcium, gypsum was used to recycle the waste which was massively produces in the phosphoric acid production. The gypsum waste, the raw material of CaCl2 supernatant, was dissolved in concentrated HCl and then precipitated as calcium oxalate (CaC2O4 by addition of ammonium oxalate. The CaCl2 was obtained by dissolving the CaC2O4 with HCl 3M. The crystals were grown at room temperature in silica gel and characterized by AAS, FTIR and powder XRD. The optimum crystal growth condition, which is pH of gel, CaCl2 concentration and growth time, were investigated. The result shows that at optimum condition of pH 5.80, CaCl2 concentrations of 1.2 M, and growth time of 144 hours, colorless crystals with the longest size of 3 mm, were obtained (72.57%. Characterization of the synthesized crystal by AAS indicates that the obtained crystal has high purity. Meanwhile, analysis by FTIR spectra shows a Ca–F peak at 775 cm-1, and powder-XRD analysis confirms that the obtained crystal was fluorite (CaF2. © 2012 BCREC UNDIP. All rights reservedReceived: 11st April 2012; Revised: 4th June 2012; Accepted: 13rd June 2012[How to Cite: M.M. Khunur, A. Risdianto, S. Mutrofin, Y.P. Prananto. (2012. Synthesis of Fluorite (CaF2 Crystal from Gypsum Waste of Phosphoric Acid Factory in Silica Gel. Bulletin of Chemical Reaction Engineering & Catalysis, 7 (1: 71-77.  doi:10.9767/bcrec.7.1.3171.71-77 ][How to Link / DOI: http://dx.doi.org/10.9767/bcrec.7.1.3171.71-77 ] | View in 

  7. The immiscible aqueous solutions of alkyl phosphates. Study for the purpose of uranium extraction from phosphoric acid solutions

    International Nuclear Information System (INIS)

    Mauborgne, Bernard

    1979-01-01

    Systems of immiscible aqueous solutions composed by a phase rich in mineral salt and by another phase almost totally containing an organic salt, have been studied for years, with quaternary ammonium salts with an organic cation. The objective of this research is to study systems symmetric to the previous ones, i.e. with organic anions such as alkyl phosphates, and then to try to understand mechanisms of extraction of metals in these environments. Based on properties of immiscible aqueous solutions, an original three-phase process of liquid-liquid extraction has been developed, and is used to separate uranium in phosphoric acids with better performance than the existing industrial processes [fr

  8. Auger electron spectroscopy and Rutherford backscattering studies of copper in 2024-T3 aluminum following electrochemical anodization in phosphoric acid

    Science.gov (United States)

    Solomon, J. S.

    1981-05-01

    The effects of the electrochemical anodization of dioxidized 2024-T3 aluminum on copper were characterized by Auger electron spectroscopy and Rutherford backscattering. Anodization was performed in phosphoric acid at constant potential. Data is presented which shows that constant potential anodization of 2024-T3 is more efficient than aluminum in terms of oxide growth rates for short anodization times. However the maximum anodic oxide thickness achievable on the alloy is less than the pure metal. Copper is shown to be enriched at the oxide metal interface because of its diffusion from the bulk during anodization. The presence of copper at the oxide-metal interface is shown to affect oxide morphology.

  9. Porous polybenzimidazole membranes doped with phosphoric acid: Preparation and application in high-temperature proton-exchange-membrane fuel cells

    International Nuclear Information System (INIS)

    Li, Jin; Li, Xiaojin; Yu, Shuchun; Hao, Jinkai; Lu, Wangting; Shao, Zhigang; Yi, Baolian

    2014-01-01

    Highlights: • Porous polybenzimidazole membrane was prepared with glucose as porogen. • Phosphoric acid content was as high as 15.7 mol H 3 PO 4 per PBI repeat unit. • 200 h Constant current density test was carried out at 150 °C. • Degradation was due to the gap between membrane and catalyst layer. - Abstract: In this paper, the preparation and characterization of porous polybenzimidazole membranes doped with phosphoric acid were reported. For the preparation of porous polybenzimidazole membranes, glucose and saccharose were selected as porogen and added into PBI resin solution before solvent casting. The prepared porous PBI membranes had high proton conductivity and high content of acid doping at room temperature with 15.7 mol H 3 PO 4 per PBI repeat unit, much higher than pure PBI membrane at the same condition. Further, the performance and stability of the porous PBI membrane in high-temperature proton-exchange-membrane fuel cells was tested. It was found that the cell performance remained stable during 200 h stability test under a constant current discharge of 0.5 A cm −2 except for the last fifty hours. The decay in the last fifty hours was ascribed to the delamination between the catalyst layer and membrane increasing the charge-transfer resistance

  10. Inorganic polymers from laterite using activation with phosphoric acid and alkaline sodium silicate solution: Mechanical and microstructural properties

    International Nuclear Information System (INIS)

    Enzo Ferrari, Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy))" data-affiliation=" (Dipartimento di Ingegneria Enzo Ferrari, Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy))" >Lassinantti Gualtieri, Magdalena; Enzo Ferrari, Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy))" data-affiliation=" (Dipartimento di Ingegneria Enzo Ferrari, Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy))" >Romagnoli, Marcello; Pollastri, Simone; Gualtieri, Alessandro F.

    2015-01-01

    Geopolymers from laterite, an iron-rich soil available in developing countries, have great potential as building materials. In this work, laterite from Togo (Africa) was used to prepare geopolymers using both phosphoric acid and alkaline sodium silicate solution. Microstructural properties were investigated by scanning electron microscopy, X-ray powder diffraction and mercury porosimetry, whereas thermal properties were evaluated by thermal analyses. The local environment of iron was studied by X-ray Absorption Spectroscopy (XANES region). The mechanical properties were determined. Modulus of Rupture and Young's modulus fell in the ranges 3.3–4.5 MPa and 12–33 GPa, respectively, rendering the materials good candidates for construction purposes. Heating above 900 °C results in weight-gain, presumably due to iron redox reactions. X-ray Absorption Spectroscopy data evidence changes in the chemical and structural environments of iron following thermal treatment of geopolymers. These changes indicate interaction between the geopolymer structure and iron during heating, possibly leading to redox properties. -- Highlights: •Geopolymerization of laterite is promising for fabrication of building materials. •Both phosphoric acid and alkaline sodium silicate solution can be used for activation. •Thermally activated redox properties of the inorganic polymers were observed

  11. Inorganic polymers from laterite using activation with phosphoric acid and alkaline sodium silicate solution: Mechanical and microstructural properties

    Energy Technology Data Exchange (ETDEWEB)

    Lassinantti Gualtieri, Magdalena, E-mail: magdalena.gualtieri@unimore.it [Dipartimento di Ingegneria " Enzo Ferrari" , Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy); Romagnoli, Marcello [Dipartimento di Ingegneria " Enzo Ferrari" , Università degli studi di Modena e Reggio Emilia, Via Vignolese 905/a, I-41125 Modena (Italy); Pollastri, Simone; Gualtieri, Alessandro F. [Dipartimento di Scienze Chimiche e Geologiche, Università degli studi di Modena e Reggio Emilia, Via S. Eufemia 19I, I-41121 Modena (Italy)

    2015-01-15

    Geopolymers from laterite, an iron-rich soil available in developing countries, have great potential as building materials. In this work, laterite from Togo (Africa) was used to prepare geopolymers using both phosphoric acid and alkaline sodium silicate solution. Microstructural properties were investigated by scanning electron microscopy, X-ray powder diffraction and mercury porosimetry, whereas thermal properties were evaluated by thermal analyses. The local environment of iron was studied by X-ray Absorption Spectroscopy (XANES region). The mechanical properties were determined. Modulus of Rupture and Young's modulus fell in the ranges 3.3–4.5 MPa and 12–33 GPa, respectively, rendering the materials good candidates for construction purposes. Heating above 900 °C results in weight-gain, presumably due to iron redox reactions. X-ray Absorption Spectroscopy data evidence changes in the chemical and structural environments of iron following thermal treatment of geopolymers. These changes indicate interaction between the geopolymer structure and iron during heating, possibly leading to redox properties. -- Highlights: •Geopolymerization of laterite is promising for fabrication of building materials. •Both phosphoric acid and alkaline sodium silicate solution can be used for activation. •Thermally activated redox properties of the inorganic polymers were observed.

  12. Enantioselective Synthesis of α-Mercapto-β-amino Esters via Rh(II)/Chiral Phosphoric Acid-Cocatalyzed Three-Component Reaction of Diazo Compounds, Thiols, and Imines.

    Science.gov (United States)

    Xiao, Guolan; Ma, Chaoqun; Xing, Dong; Hu, Wenhao

    2016-12-02

    An enantioselective method for the synthesis of α-mercapto-β-amino esters has been developed via a rhodium(II)/chiral phosphoric acid-cocatalyzed three-component reaction of diazo compounds, thiols, and imines. This transformation is proposed to proceed through enantioselective trapping of the sulfonium ylide intermediate generated in situ from the diazo compound and thiol by the phosphoric acid-activated imine. With this method, a series of α-mercapto-β-amino esters were obtained in good yields with moderate to good stereoselectivities.

  13. Humic flotation of wet process phosphoric acid as a pretreatment step in the recovery of uranium

    International Nuclear Information System (INIS)

    Lopez, J.G.; Barnhart, V.J.

    1983-01-01

    An acidic solution containing metal values and also containing humic acid impurities, is purified by: (1) forming a gas in the acid solution, (2) adding high molecular weight anionic organic flocculant in a volume ratio of gas containing acid solution to flocculant of 1,000:0.002 to 0.10, to form a bottom, purified, aqueous acidic phase containing metal values and a top flocculated humic acid impurities froth phase and (3) removing the humic acid froth phase

  14. Thermoluminescent phosphor

    Science.gov (United States)

    Lasky, Jerome B.; Moran, Paul R.

    1978-01-01

    A thermoluminescent phosphor comprising LiF doped with boron and magnesium is produced by diffusion of boron into a conventional LiF phosphor doped with magnesium. Where the boron dopant is made to penetrate only the outer layer of the phosphor, it can be used to detect shallowly penetrating radiation such as tritium beta rays in the presence of a background of more penetrating radiation.

  15. Isolation and structural characterization of sugarcane bagasse lignin after dilute phosphoric acid plus steam explosion pretreatment and its effect on cellulose hydrolysis

    Science.gov (United States)

    Jijiao Zeng; Zhaohui Tong; Letian Wang; J.Y. Zhu; Lonnie Ingram

    2014-01-01

    The structure of lignin after dilute phosphoric acid plus steam explosion pretreatment process of sugarcane bagasse in a pilot scale and the effect of the lignin extracted by ethanol on subsequent cellulose hydrolysis were investigated. The lignin structural changes caused by pretreatment were identified using advanced nondestructive techniques such as gel permeation...

  16. Natural Radiation in byproducts of the production of phosphoric acid; Radiacao natural em residuos gerados no processo de producao de acido fosforico

    Energy Technology Data Exchange (ETDEWEB)

    Silveira, Marcilei A. Guazzelli da; Cardoso, L.L., E-mail: marcilei@fei.edu.br [Centro Universitario da FEI, Sao Bernardo do Campo, SP (Brazil); Medina, N.H. [Universidade de Sao Paulo (USP), Sao Paulo, SP (Brazil). Institutlo de Fisica

    2014-07-01

    Natural radiation is the largest source of radiation exposure to which man is subject. It is formed basically by cosmic radiation and the radionuclides present in the Earth crust, as {sup 40}K and the elements of the decay series of {sup 232}Th and {sup 238}U. Phosphate ores, which constitutes the raw material for the production of phosphoric acid, have a high rate of natural radiation from the decay series of {sup 232}Th and {sup 238}U. Phosphogypsum, which is naturally radioactivity, is a by-product of the production of phosphoric acid by the wet method. For each ton of phosphoric acid it is produced about 4.5 tons of phosphogypsum. This work presents the analysis of samples collected in all stages of the manufacturing process of phosphoric acid, which generates the phosphogypsum. Gamma-ray spectrometry was used to measure the concentration of the elements of the decay series of {sup 232}Th and {sup 238}U. All analyzed samples showed a high concentration of radionuclides, promoting the need for further steps in the process in order to reduce the presence of such radionuclides in the phosphogypsum. The results indicate the radionuclide {sup 238}U has higher contribution in some samples of the intermediate stages of the process. All samples exceeded the international average range of human exposure to terrestrial gamma radiation, which is 0.3 to 1.0 mSv/year. (author)

  17. A new oxidimetric reagent-potassium dichromate in a strong phosphoric acid medium-VIII Potentiometric titration of molybdenum(VI) and vanadium(V).

    Science.gov (United States)

    Muralikrishna, U; Rao, G G

    1968-01-01

    A new titrimetric method is described for the determination of molybdenum(VI) involving prior reduction to Mo(V) with an excess of Fe(II) in a concentrated phosphoric acid solution, followed by titration with dichromate. The titration can be done at room temperature and without protective atmosphere. Uranium interferes, but vanadium may be determined simultaneously.

  18. Ion conduction mechanisms and thermal properties of hydrated and anhydrous phosphoric acids studied with 1H, 2H, and 31P NMR.

    Science.gov (United States)

    Aihara, Yuichi; Sonai, Atsuo; Hattori, Mineyuki; Hayamizu, Kikuko

    2006-12-14

    To understand the behaviors of phosphoric acids in fuel cells, the ion conduction mechanisms of phosphoric acids in condensed states without free water and in a monomer state with water were studied by measuring the ionic conductivity (sigma) using AC impedance, thermal properties, and self-diffusion coefficients (D) and spin-lattice relaxation times (T1) with multinuclear NMR. The self-diffusion coefficient of the protons (H+ or H3O+), H2O, and H located around the phosphate were always larger than the diffusion coefficients of the phosphates and the disparity increased with increasing phosphate concentration. The diffusion coefficients of the samples containing D2O paralleled those in the protonated samples. Since the 1H NMR T1 values exhibited a minimum with temperature, it was possible to determine the correlation times and they were found to be of nanosecond order for a distance of nanometer order for a flip. The agreement of the ionic conductivities measured directly and those calculated from the diffusion coefficients indicates that the ion conduction obeys the Nernst-Einstein equation in the condensed phosphoric acids. The proton diffusion plays a dominant role in the ion conduction, especially in the condensed phosphoric acids.

  19. Titrimetric determination of uranium in low-grade ores by the ferrous ion-phosphoric acid reduction method

    International Nuclear Information System (INIS)

    Hitchen, A.; Zechanowitsch, G.

    1980-01-01

    The modification and extension of the U.S.A.E.C. ferrous ion-phosphoric acid reduction method for the determination of uranium in high-grade or relatively pure material to a method for the determination of uranium with a high accuracy and precision, in ores containing 0.004 to 7% U is described. It is simple, rapid and requires no prior separations from elements that, in other methods, frequently interfere. For sample materials having very high concentrations of interfering elements, a prior concentration step using extraction with tri-n-octylphosphine oxide is described, but it is shown that, for most low-grade ores, this step is unnecessary. (author)

  20. Effect of sol aging time on the anti-reflective properties of silica coatings templated with phosphoric acid

    Directory of Open Access Journals (Sweden)

    Wen Wen

    Full Text Available Silica anti-reflective coatings have been prepared by a sol–gel dip-coating process using the sol containing phosphoric acid as a pore-forming template. The effect of the aging time of the sol on the anti-reflective properties has been investigated. The surface topography of the silica AR coatings has been characterized. With increasing sol aging time, more over-sized pores larger than 100 nm are formed in the silica coatings. These could act as scattering centers, scattering visible light and thereby lowering transmittance. The optimal aging time was identified as 1 day, and the corresponding silica coatings showed a maximum transmittance of 99.2%, representing an 8% increase compared to the bare glass substrate. Keywords: Thin films, Anti-reflective coatings, Aging, Dip-coating, Sol–gel preparation

  1. On the complexing of phosphoric acid vinyl esters with praseodymium (3) and europium (3) nitrates in acetonitrile

    International Nuclear Information System (INIS)

    Goryushko, A.G.; Gololobov, Yu.G.; Boldeskul, A.E.; Oganesyan, A.S.; Yartsev, V.G.

    1990-01-01

    By the methods of electron, IR and PMR spectroscopy interaction of vinyl esters of phosphoric acid with praseodymium (3) and europium (3) nitrates in acetonitrile solutions has been studied. It is shown that the character of metal-ligand interaction is determined by chemical nature of the ligands: for a compound of ionic structure partially covalent bond is formed, and for a compound of betaine structure the interaction has mainly dipole character. Addition of molecule with betaine structure to praseodymium nitrate causes a change in geometry of Pr 3+ close surrounding and increase in its coordination number. The possibility of formation of the complex with metal-ligand ratio equal to 1:3 is shown

  2. Effects of Chlorine Ions on the Dissolution Mechanism of Cu Thin Film in Phosphoric Acid Based Solution.

    Science.gov (United States)

    Seo, Bo-Hyun; Kim, Byoung O; Seo, Jong Hyun

    2015-10-01

    The dissolution mechanisms of Cu thin film were studied with a focus on the effect of chlorine ion concentrations in mixture solutions of phosphoric and nitric acid. The dissolution behaviors of Cu thin film were investigated by using potentio-dynamic curves and impedance spectroscopy with varying chlorine ion concentrations. The copper dissolution rate decreased and as a result of this change, CuCl, salt films formed on the Cu surface in the presence of chlorine ions in the mixture solution. Such behavior was interpreted as being competitive adsorption between chlorine and nitrate ions on the copper surface. The passive oxide film on the Cu surface was further investigated in detail using X-ray photoelectron spectroscopy in both the absence and presence of differing chlorine ion concentrations.

  3. Adsorption of organic matter contained in industrial phosphoric acid onto bentonite: Batch contact time and kinetic study

    International Nuclear Information System (INIS)

    Mellah, Abdelhamid

    1992-12-01

    The soluble organic matter present in industrial phosphoric acid can strongly affect the uranium recovery during its solvent extraction by forming stable foams and emulsions. The removal of these organics is an important step both for the production of decontaminated fertilizers and the successful recovery of uranium. The equilibrium isotherms of organic matter adsorption onto bentonite show that the data correlated well with freundlich's model and that the adsorption is physical in nature. the maximum monomolecular capacity (Qo) according to the Langmuir model is 153 mg/g for an initial organic matter concentration of 251.5 mg/1, at 30 oC. The operating parameters (agitation speed, solid/liquid ratio, temperature, particle size and initial organic matter concentration) influenced the rate of adsorption. The adsorption isotherm of uranium onto bentonite exhibits and anomalous shape similar to the Z-type isotherm reported by Giles et al

  4. Studies on entrained DNPPA separation by charcoal adsorption from aqueous solutions generated during uranium recovery from strong phosphoric acid

    International Nuclear Information System (INIS)

    Singh, D.K.; Vijayalakshmi, R.; Singh, H.

    2010-01-01

    During the separation of metal ions by solvent extraction technique in hydrometallurgical operations, organic solvents either get entrained or dissolved in various types of aqueous streams, which need to be separated out to prevent environmental pollution and solvent loss. Generally entrained solvents are separated on plant scale by parallel plate separators or by froth floatation cells, while the dissolved solvents are recovered either by organic diluent wash or by charcoal adsorption. A novel process has been developed to recover uranium from merchant grade phosphoric acid (MGA) employing synergistic mixture of DNPPA (di-nonyl phenyl phosphoric acid ) and TOPO (tri-n-octyl phosphine oxide) dissolved in petrofin. After recovery of uranium, MGA has to be returned to the host company for the production of fertilizer. This MGA has to be free from any contamination due to DNPPA and TOPO. Separation of DNPPA and TOPO from MGA by diluent wash method has been reported. There is no information available in literature for the separation of DNPPA and TOPO from such aqueous streams by carbon adsorption. The present investigation describes the methodology based on charcoal adsorption study (batch and continuous column operation) to separate DNPPA from MGA. Three different types of charcoal namely coconut shell based, coal based and pelletized charcoal were evaluated for DNPPA separation from MGA containing 100 mg/L DNPPA. It was found that the % DNPPA adsorptions in single contact (0.5g C/50 ml) were 57, 34 and 10 in coconut shell, coal based and pelletised charcoal respectively. Based on the results, the coconut shell based charcoal was selected for further study. Adsorption of DNPPA by coconut shell based charcoal was investigated by carrying out the experiments with 50 ml MGA containing 770 mg/L DNPPA by adding 1 to 7 g charcoal respectively in separate beakers

  5. Effect of Reduced Phosphoric Acid Pre-etching Times 
on Enamel Surface Characteristics and Shear Fatigue Strength Using Universal Adhesives.

    Science.gov (United States)

    Tsujimoto, Akimasa; Fischer, Nicholas; Barkmeier, Wayne; Baruth, Andrew; Takamizawa, Toshiki; Latta, Mark; Miyazaki, Masashi

    2017-01-01

    To examine the effect of reduced phosphoric acid pre-etching times on enamel fatigue bond strength of universal adhesives and surface characteristics by using atomic force microscopy (AFM). Three universal adhesives were used in this study (Clearfil Universal Bond [C], G-Premio Bond [GP], Scotchbond Universal Adhesive [SU]). Four pre-etching groups were employed: enamel pre-etched with phosphoric acid and immediately rinsed with an air-water spray, and enamel pre-etched with phosphoric acid for 5, 10, or 15 s. Ground enamel was used as the control group. For the initial bond strength test, 15 specimens per etching group for each adhesive were used. For the shear fatigue test, 20 specimens per etching group for each adhesive were loaded using a sine wave at a frequency of 20 Hz for 50,000 cycles or until failure occurred. Initial shear bond strengths and fatigue shear strengths of composite adhesively bonded to ground and pre-etched enamel were determined. AFM observations of ground and pre-etched enamel were also conducted, and surface roughness as well as surface area were evaluated. The initial shear bond strengths and fatigue shear strengths of the universal adhesives in the pre-etched groups were significantly higher than those of the control group, and were not influenced by the pre-etching time. Significantly higher surface roughness and surface area of enamel surfaces in pre-etched groups were observed compared with those in the control group. While the surface area was not significantly influenced by etching time, surface roughness of the enamel surfaces in the pre-etched groups significantly increased with pre-etching time. The results of this in vitro study suggest that reduced phosphoric acid pre-etching times do not impair the fatigue bond strength of universal adhesives. Although fatigue bond strength and surface area were not influenced by phosphoric-acid etching times, surface roughness increased with increasing etching time.

  6. Hydrometallurgical recovery of metal values from sulfuric acid leaching liquor of spent lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Xiangping; Chen, Yongbin; Zhou, Tao, E-mail: zhoutao@csu.edu.cn; Liu, Depei; Hu, Hang; Fan, Shaoyun

    2015-04-15

    Highlights: • Selective precipitation and solvent extraction were adopted. • Nickel, cobalt and lithium were selectively precipitated. • Co-D2EHPA was employed as high-efficiency extraction reagent for manganese. • High recovery percentages could be achieved for all metal values. - Abstract: Environmentally hazardous substances contained in spent Li-ion batteries, such as heavy metals and nocuous organics, will pose a threat to the environment and human health. On the other hand, the sustainable recycling of spent lithium-ion batteries may bring about environmental and economic benefits. In this study, a hydrometallurgical process was adopted for the comprehensive recovery of nickel, manganese, cobalt and lithium from sulfuric acid leaching liquor from waste cathode materials of spent lithium-ion batteries. First, nickel ions were selectively precipitated and recovered using dimethylglyoxime reagent. Recycled dimethylglyoxime could be re-used as precipitant for nickel and revealed similar precipitation performance compared with fresh dimethylglyoxime. Then the separation of manganese and cobalt was conducted by solvent extraction method using cobalt loaded D2EHPA. And McCabe–Thiele isotherm was employed for the prediction of the degree of separation and the number of extraction stages needed at specific experimental conditions. Finally, cobalt and lithium were sequentially precipitated and recovered as CoC{sub 2}O{sub 4}⋅2H{sub 2}O and Li{sub 2}CO{sub 3} using ammonium oxalate solution and saturated sodium carbonate solution, respectively. Recovery efficiencies could be attained as follows: 98.7% for Ni; 97.1% for Mn, 98.2% for Co and 81.0% for Li under optimized experimental conditions. This hydrometallurgical process may promise a candidate for the effective separation and recovery of metal values from the sulfuric acid leaching liquor.

  7. Hydrometallurgical recovery of metal values from sulfuric acid leaching liquor of spent lithium-ion batteries

    International Nuclear Information System (INIS)

    Chen, Xiangping; Chen, Yongbin; Zhou, Tao; Liu, Depei; Hu, Hang; Fan, Shaoyun

    2015-01-01

    Highlights: • Selective precipitation and solvent extraction were adopted. • Nickel, cobalt and lithium were selectively precipitated. • Co-D2EHPA was employed as high-efficiency extraction reagent for manganese. • High recovery percentages could be achieved for all metal values. - Abstract: Environmentally hazardous substances contained in spent Li-ion batteries, such as heavy metals and nocuous organics, will pose a threat to the environment and human health. On the other hand, the sustainable recycling of spent lithium-ion batteries may bring about environmental and economic benefits. In this study, a hydrometallurgical process was adopted for the comprehensive recovery of nickel, manganese, cobalt and lithium from sulfuric acid leaching liquor from waste cathode materials of spent lithium-ion batteries. First, nickel ions were selectively precipitated and recovered using dimethylglyoxime reagent. Recycled dimethylglyoxime could be re-used as precipitant for nickel and revealed similar precipitation performance compared with fresh dimethylglyoxime. Then the separation of manganese and cobalt was conducted by solvent extraction method using cobalt loaded D2EHPA. And McCabe–Thiele isotherm was employed for the prediction of the degree of separation and the number of extraction stages needed at specific experimental conditions. Finally, cobalt and lithium were sequentially precipitated and recovered as CoC 2 O 4 ⋅2H 2 O and Li 2 CO 3 using ammonium oxalate solution and saturated sodium carbonate solution, respectively. Recovery efficiencies could be attained as follows: 98.7% for Ni; 97.1% for Mn, 98.2% for Co and 81.0% for Li under optimized experimental conditions. This hydrometallurgical process may promise a candidate for the effective separation and recovery of metal values from the sulfuric acid leaching liquor

  8. Role of keto–enol tautomerization in a chiral phosphoric acid catalyzed asymmetric thiocarboxylysis of meso-epoxide: a DFT study

    KAUST Repository

    Ajitha, Manjaly John; Huang, Kuo-Wei

    2015-01-01

    The mechanism of a chiral phosphoric acid catalyzed thiocarboxylysis of meso-epoxide was investigated by density functional theory (DFT) calculations (M06-2X). The nucleophilic ring opening of epoxide by thiobenzoic acid was found to proceed via a concerted termolecular transition state with a simultaneous dual proton transfer to yield the β-hydroxy thioester product. Electrostatic interactions together with the steric environment inside the chiral catalyst play an important role in determining the enantioselectivity of the reaction.

  9. Role of keto–enol tautomerization in a chiral phosphoric acid catalyzed asymmetric thiocarboxylysis of meso-epoxide: a DFT study

    KAUST Repository

    Ajitha, Manjaly John

    2015-09-15

    The mechanism of a chiral phosphoric acid catalyzed thiocarboxylysis of meso-epoxide was investigated by density functional theory (DFT) calculations (M06-2X). The nucleophilic ring opening of epoxide by thiobenzoic acid was found to proceed via a concerted termolecular transition state with a simultaneous dual proton transfer to yield the β-hydroxy thioester product. Electrostatic interactions together with the steric environment inside the chiral catalyst play an important role in determining the enantioselectivity of the reaction.

  10. (Di­methyl­phosphor­yl)methanaminium hydrogen oxalate–oxalic acid (2/1)

    Science.gov (United States)

    Bialek, Sebastian; Clemens, Rebecca; Reiss, Guido J.

    2014-01-01

    The reaction of (di­methyl­phosphor­yl)methanamine (dpma) with oxalic acid in ethanol yielded the title solvated salt, C3H11NOP+·C2HO4 −·0.5C2H2O4. Its asymmetric unit consists of one dpmaH+ cation, one hydrogen oxalate anion and a half-mol­ecule of oxalic acid located around a twofold rotation axis. The H atom of the hydrogen oxalate anion is statistically disordered over two positions that are trans to each other. The hydrogen oxalate monoanion is not planar (bend angle ∼16°) whereas the oxalic acid molecule shows a significantly smaller bend angle (∼7°). In the crystal, the components are connected by strong O—H⋯O and much weaker N—H⋯O hydrogen bonds, leading to the formation of layers extending parallel to (001). The structure was refined from a racemically twinned crystal with twin components in an approximate 1:1 ratio. PMID:24765013

  11. Nanoporous anodic aluminum oxide with a long-range order and tunable cell sizes by phosphoric acid anodization on pre-patterned substrates

    Science.gov (United States)

    Surawathanawises, Krissada; Cheng, Xuanhong

    2014-01-01

    Nanoporous anodic aluminum oxide (AAO) has been explored for various applications due to its regular cell arrangement and relatively easy fabrication processes. However, conventional two-step anodization based on self-organization only allows the fabrication of a few discrete cell sizes and formation of small domains of hexagonally packed pores. Recent efforts to pre-pattern aluminum followed with anodization significantly improve the regularity and available pore geometries in AAO, while systematic study of the anodization condition, especially the impact of acid composition on pore formation guided by nanoindentation is still lacking. In this work, we pre-patterned aluminium thin films using ordered monolayers of silica beads and formed porous AAO in a single-step anodization in phosphoric acid. Controllable cell sizes ranging from 280 nm to 760 nm were obtained, matching the diameters of the silica nanobead molds used. This range of cell size is significantly greater than what has been reported for AAO formed in phosphoric acid in the literature. In addition, the relationships between the acid concentration, cell size, pore size, anodization voltage and film growth rate were studied quantitatively. The results are consistent with the theory of oxide formation through an electrochemical reaction. Not only does this study provide useful operational conditions of nanoindentation induced anodization in phosphoric acid, it also generates significant information for fundamental understanding of AAO formation. PMID:24535886

  12. Influence of anodization parameters on the volume expansion of anodic aluminum oxide formed in mixed solution of phosphoric and oxalic acids

    Science.gov (United States)

    Kao, Tzung-Ta; Chang, Yao-Chung

    2014-01-01

    The growth of anodic alumina oxide was conducted in the mixed solution of phosphoric and oxalic acids. The influence of anodizing voltage, electrolyte temperature, and concentration of phosphoric and oxalic acids on the volume expansion of anodic aluminum oxide has been investigated. Either anodizing parameter is chosen to its full extent of range that allows the anodization process to be conducted without electric breakdown and to explore the highest possible volume expansion factor. The volume expansion factors were found to vary between 1.25 and 1.9 depending on the anodizing parameters. The variation is explained in connection with electric field, ion transport number, temperature effect, concentration, and activity of acids. The formation of anodic porous alumina at anodizing voltage 160 V in 1.1 M phosphoric acid mixed with 0.14 M oxalic acid at 2 °C showed the peak volume expansion factor of 1.9 and the corresponding moderate growth rate of 168 nm/min.

  13. Preparation and physical properties of (PVA0.7(NaBr0.3(H3PO4xM solid acid membrane for phosphoric acid – Fuel cells

    Directory of Open Access Journals (Sweden)

    F. Ahmad

    2013-03-01

    Full Text Available A solid acid membranes based on poly (vinyl alcohol (PVA, sodium bromide (NaBr and phosphoric acid (H3PO4 were prepared by a solution casting method. The morphological, IR, electrical and optical properties of the (PVA0.7(NaBr0.3(H3PO4xM solid acid membranes where x = 0.00, 0.85, 1.7, 3.4, 5.1 M were investigated. The variation of film morphology was examined by scanning electron microscopy (SEM studies. FTIR spectroscopy has been used to characterize the structure of polymer and confirms the complexation of phosphoric acid with host polymeric matrix. The temperature dependent nature of ionic conductivity and the impedance of the polymer electrolytes were determined along with the associated activation energy. The ionic conductivity at room temperature was found to be strongly depends on the H3PO4 concentration which it has been achieved to be of the order 4.3 × 10−3 S/cm at ambient temperature. Optical measurements showed a decrease in optical band gap and an increase in band tail width with the increase of phosphoric acid. The data shows that the (PVA0.7(NaBr0.3(H3PO4xM solid acid membrane is promising for intermediate temperature phosphoric acid fuel cell applications.

  14. Radiological, chemical and morphological characterizations of phosphate rock and phosphogypsum from phosphoric acid factories in SW Spain

    Energy Technology Data Exchange (ETDEWEB)

    Renteria-Villalobos, Marusia, E-mail: marusia@us.es [Applied Nuclear Physics Group, University of Seville, ETS Arquitectura, Departamento de Fisica Aplicada, Avda. Reina Mercedes s/n, 41012 Seville (Spain); Advanced Materials Research Center (CIMAV), Miguel de Cervantes 120, 31109 Chihuahua (Mexico); Vioque, Ignacio, E-mail: ivioque@us.es [Applied Nuclear Physics Group, University of Seville, ETS Arquitectura, Departamento de Fisica Aplicada, Avda. Reina Mercedes s/n, 41012 Seville (Spain); Mantero, Juan, E-mail: manter@us.es [Applied Nuclear Physics Group, University of Seville, ETS Arquitectura, Departamento de Fisica Aplicada, Avda. Reina Mercedes s/n, 41012 Seville (Spain); Manjon, Guillermo, E-mail: manjon@us.es [Applied Nuclear Physics Group, University of Seville, ETS Arquitectura, Departamento de Fisica Aplicada, Avda. Reina Mercedes s/n, 41012 Seville (Spain)

    2010-09-15

    In this work, radiological, chemical, and also morphological characterization was performed in phosphate rock and phosphogypsum samples, in order to understand the behavior of toxic elements. Characterization was carried out using X-ray diffraction (XRD), X-ray fluorescence (XRF), gamma spectrometry and scanning electron microscopy with energy-dispersive X-ray analysis (SEM-EDX). Our results show that the phosphate rock was mainly composed of fluorapatite, calcite, perovskite, quartz, magnetite, pyrite and kaolinite, whereas phosphogypsum only exhibited dihydrated calcium sulfate. The activity concentration of U-series radioisotopes in phosphate rock was around 1640 Bq/kg. {sup 226}Ra and {sup 210}Pb tend to be distributed into phosphogypsum by up to 80%, whereas the fraction of U-isotopes is 10%. The most abundant trace elements in phosphate rock were Sr, Cr, V, Zn, Y, Ni and Ba. Some elements, such as Ba, Cd, Cu, La, Pb, Se, Sr, Th and Y, were enriched in the phosphogypsum. This enrichment may be attributed to an additional input associated to the sulfuric acid used for the phosphoric acid production. Furthermore, results from SEM-EDX demonstrated that toxic elements are not distributed homogeneously into phosphogypsum. Most of these elements are concentrated in particles <20 {mu}m of high porosity, and could be easily mobilized by leaching and/or erosion.

  15. Radiological, chemical and morphological characterizations of phosphate rock and phosphogypsum from phosphoric acid factories in SW Spain

    International Nuclear Information System (INIS)

    Renteria-Villalobos, Marusia; Vioque, Ignacio; Mantero, Juan; Manjon, Guillermo

    2010-01-01

    In this work, radiological, chemical, and also morphological characterization was performed in phosphate rock and phosphogypsum samples, in order to understand the behavior of toxic elements. Characterization was carried out using X-ray diffraction (XRD), X-ray fluorescence (XRF), gamma spectrometry and scanning electron microscopy with energy-dispersive X-ray analysis (SEM-EDX). Our results show that the phosphate rock was mainly composed of fluorapatite, calcite, perovskite, quartz, magnetite, pyrite and kaolinite, whereas phosphogypsum only exhibited dihydrated calcium sulfate. The activity concentration of U-series radioisotopes in phosphate rock was around 1640 Bq/kg. 226 Ra and 210 Pb tend to be distributed into phosphogypsum by up to 80%, whereas the fraction of U-isotopes is 10%. The most abundant trace elements in phosphate rock were Sr, Cr, V, Zn, Y, Ni and Ba. Some elements, such as Ba, Cd, Cu, La, Pb, Se, Sr, Th and Y, were enriched in the phosphogypsum. This enrichment may be attributed to an additional input associated to the sulfuric acid used for the phosphoric acid production. Furthermore, results from SEM-EDX demonstrated that toxic elements are not distributed homogeneously into phosphogypsum. Most of these elements are concentrated in particles <20 μm of high porosity, and could be easily mobilized by leaching and/or erosion.

  16. Thermodynamic and structural of the water - dodecane - bis(ethyl-2-hexyl) phosphoric acid and its sodium salt

    International Nuclear Information System (INIS)

    Lovera, Jacqueline

    1985-01-01

    This research thesis reports the study of the appearance and disappearance of the 'third phase' obtained during the salification of the bis(ethyl-2 hexyl) phosphoric acid (HDEHP) diluted in dodecane, by sodium aqueous solutions. After a large bibliographical study on the properties of the intervening compounds (extraction of metallic cation by the acid, parameters influencing the 'third phase' appearance, surfactant properties, direct and inverse micelles, formation of para-crystalline phases), the author presents chemical experimental methods: liquid-liquid extraction tests, tests by the synthetic way, preparation of reactants, dosing method, methods of chemical analysis). Then, she reports and discusses experimental results in terms of determination of phase diagrams at 25 C, of composition by weight of the third phase, of influence of the apolar diluent, and of influence of the electrolyte. Physical experimental methods are then presented (differential calorimetric analysis, NMR, small angle X-ray scattering, light scattering, polarised light microscopy, constrained phase microscopy, photography, infrared spectroscopy, conductometry, transmission electron micrography, volumetric mass measurements, surface and interface tension measurements, viscoelasticity measurements) and their results are discussed and interpreted [fr

  17. Phosphoric acid based pretreatment of switchgrass and fermentation of entire slurry to ethanol using a simplified process.

    Science.gov (United States)

    Wu, Wei; Rondon, Vanessa; Weeks, Kalvin; Pullammanappallil, Pratap; Ingram, Lonnie O; Shanmugam, K T

    2018-03-01

    Switchgrass (Alamo) was pretreated with phosphoric acid (0.75 and 1%, w/w) at three temperatures (160, 175 and 190 °C) and time (5, 7.5 and 10 min) using a steam gun. The slurry after pretreatment was liquefied by enzymes and the released sugars were fermented in a simultaneous saccharification and co-fermentation process to ethanol using ethanologenic Escherichia coli strain SL100. Among the three variables in pretreatment, temperature and time were critical in supporting ethanol titer and yield. Enzyme hydrolysis significantly increased the concentration of furans in slurries, apparently due to release of furans bound to the solids. The highest ethanol titer of 21.2 ± 0.3 g/L ethanol obtained at the pretreatment condition of 190-1-7.5 (temperature-acid concentration-time) and 10% solids loading accounted for 190 ± 2.9 g ethanol/kg of raw switch grass. This converts to 61.7 gallons of ethanol per ton of dry switchgrass, a value that is comparable to other published pretreatment conditions. Copyright © 2017 Elsevier Ltd. All rights reserved.

  18. Optimizing Available Phosphorus in Calcareous Soils Fertilized with Diammonium Phosphate and Phosphoric Acid Using Freundlich Adsorption Isotherm

    Science.gov (United States)

    Akhtar, Muhammad

    2013-01-01

    In calcareous soils, phosphorus (P) retention and immobilization take place due to precipitation and adsorption. Since soil pH is considered a major soil variable affecting the P sorption, an acidic P fertilizer could result in low P adsorption compared to alkaline one. Therefore, P adsorption from DAP and phosphoric acid (PA) required to produce desired soil solution P concentration was estimated using Freundlich sorption isotherms. Two soils from Faisalabad and T. T. Singh districts were spiked with 0, 10, and 20 % CaCO3 for 15 days. Freundlich adsorption isotherms (P = aC b/a) were constructed, and theoretical doses of PA and DAP to develop a desired soil solution P level (i.e., 0.20 mg L−1) were calculated. It was observed that P adsorption in soil increased with CaCO3. Moreover, at all the levels of CaCO3, P adsorption from PA was lower compared to that from DAP in both the soils. Consequently, lesser quantity of PA was required to produce desired solution P, 0.2 mg L−1, compared to DAP. However, extrapolating the developed relationship between soil CaCO3 contents and quantity of fertilizer to other similar textured soils needs confirmation. PMID:24307878

  19. Optimizing Available Phosphorus in Calcareous Soils Fertilized with Diammonium Phosphate and Phosphoric Acid Using Freundlich Adsorption Isotherm

    Directory of Open Access Journals (Sweden)

    Asif Naeem

    2013-01-01

    Full Text Available In calcareous soils, phosphorus (P retention and immobilization take place due to precipitation and adsorption. Since soil pH is considered a major soil variable affecting the P sorption, an acidic P fertilizer could result in low P adsorption compared to alkaline one. Therefore, P adsorption from DAP and phosphoric acid (PA required to produce desired soil solution P concentration was estimated using Freundlich sorption isotherms. Two soils from Faisalabad and T. T. Singh districts were spiked with 0, 10, and 20 % for 15 days. Freundlich adsorption isotherms ( were constructed, and theoretical doses of PA and DAP to develop a desired soil solution P level (i.e., 0.20 mg L−1 were calculated. It was observed that P adsorption in soil increased with . Moreover, at all the levels of , P adsorption from PA was lower compared to that from DAP in both the soils. Consequently, lesser quantity of PA was required to produce desired solution P, 0.2 mg L−1, compared to DAP. However, extrapolating the developed relationship between soil contents and quantity of fertilizer to other similar textured soils needs confirmation.

  20. Impact of pH and application time of meta-phosphoric acid on resin-enamel and resin-dentin bonding.

    Science.gov (United States)

    Cardenas, A F M; Siqueira, F S F; Bandeca, M C; Costa, S O; Lemos, M V S; Feitora, V P; Reis, A; Loguercio, A D; Gomes, J C

    2018-02-01

    To evaluate the immediate microshear resin-enamel bond strength (μSBS) and the immediate and 6-month microtensile bond strength (μTBS) and nanoleakage (NL) of the adhesive interface performed by different pHs of 40% meta-phosphoric acid (MPA) were compared with conventional 37% ortho-phosphoric acid (OPA) under different application times. Additionally, the enamel etching patterns were evaluated and the chemical/morphological changes induced by these differents groups were evaluated. One hundred and ninety-eight extracted human molars were randomly assigned into experimental groups according to the combination of independent variables: Acid [37% ortho-phosphoric acid (OPA), 40% meta-phosphoric acid (MPA) at pHs of: 0.5, 1 and 2] and Application Time [7, 15 and 30s]. Enamel-bond specimens were prepared and tested under μSBS. Resin-dentin beams were tested under μTBS tested immediately or after 6-months of water storage. Nanoleakage was evaluated using bonded-beams of each tooth/time-period. Enamel etching pattern and chemical and ultra-morphology analyses were also performed. The μSBS (MPa) data were subjected to a two-way repeated measures ANOVA (Acid vs. Application time). For μTBS, Acid vs application time vs storage time data were subjected to three-way ANOVA and Tukey's test (α = 0.05). MPA pH 0.5 showed μTBS similar to OPA, independently of the application time on enamel (p>0.05) or dentin (p>0.05). OPA provided higher nanoleakage values than MPA (p = 0.003). Significant decreases in TBS and increases in NL were only observed for OPA after 6 months (p = 0.001). An increase in the application time resulted in a more pronounced etching pattern for MPA. Chemical analysis showed that dentin demineralized by MPA depicted peaks of brushite and octacalcium phosphate. MPA exposed less collagen than OPA. However, optimal results for MPA were dependent on pH/application time. The use of 40% meta-phosphoric acid with a pH of 0.5 is an alternative acid

  1. Lithium recovery from shale gas produced water using solvent extraction

    International Nuclear Information System (INIS)

    Jang, Eunyoung; Jang, Yunjai; Chung, Eunhyea

    2017-01-01

    Shale gas produced water is hypersaline wastewater generated after hydraulic fracturing. Since the produced water is a mixture of shale formation water and fracturing fluid, it contains various organic and inorganic components, including lithium, a useful resource for such industries as automobile and electronics. The produced water in the Marcellus shale area contains about 95 mg/L lithium on average. This study suggests a two-stage solvent extraction technique for lithium recovery from shale gas produced water, and determines the extraction mechanism of ions in each stage. All experiments were conducted using synthetic shale gas produced water. In the first-stage, which was designed for the removal of divalent cations, more than 94.4% of Ca"2"+, Mg"2"+, Sr"2"+, and Ba"2"+ ions were removed by using 1.0 M di-(2-ethylhexyl) phosphoric acid (D2EHPA) as an extractant. In the second-stage, for lithium recovery, we could obtain a lithium extraction efficiency of 41.2% by using 1.5 M D2EHPA and 0.3 M tributyl phosphate (TBP). Lithium loss in the first-stage was 25.1%, and therefore, the total amount of lithium recovered at the end of the two-step extraction procedure was 30.8%. Through this study, lithium, one of the useful mineral resources, could be selectively recovered from the shale gas produced water and it would also reduce the wastewater treatment cost during the development of shale gas. - Highlights: • Lithium was extracted from shale gas produced water using an organic solvent. • Two-stage solvent extraction technique was applied. • Divalent cations were removed in the first stage by D2EHPA. • Lithium was selectively recovered in the second stage by using TBP with D2EHPA.

  2. Development of polysulfonic composite beads for extraction and separation of rare earths

    International Nuclear Information System (INIS)

    Yadav, K.K.; Singh, D.K.; Singh, H.; Varshney, L.

    2012-01-01

    Solvent extraction technology has been extensively applied to the practical separation of rare earth metals. Among the extractants commonly employed at present, di(2-ethylhexyl) hydrogen phosphate (D2EHPA) and 2-ethylhexyl hydrogen 2-ethylhexylphosphonate (PC-88A) are known to have advantages of high separation efficiency for rate earth metals and of low solubility in water. However, separation via solvent extraction requires multistage cycles of extraction and back extraction in order to attain favorable separation. Novel adsorbents such as solvent impregnated resins (SIRS), metal-imprinted polymers and microcapsules containing extractants might have wide applicability due to their characteristics having respective advantages of solvent extraction and the ion-exchange technique. In the present work, polymeric composite material impregnating extractants such as D2EHPA, PC88A and DNPPA were prepared and tested for rare earths recovery from chloride medium. Exploratory tests were conducted with Yttrium (taking as representative of rare earths) to evaluate the suitability of the composite beads having D2EHPA, PC88A and DNPPA. Preparation of beads comprises of following steps. Initially, a polymer solutions containing suitable amount of polymer (5 to 15% with 1% water soluble additive) in N-methyl pyrrolidone (NMP) was prepared. The above prepared solutions were then mixed with organophosphorus type of extractant namely D2EHPA, PC88A and di nonyl phenyl phosphoric acid (DNPPA). This polymer solution was gradually dropped drop wise into the water bath through a syringe needle. In the preparation, the temperature of the water was kept constant using a thermostatic unit. As as polymeric drop comes in contact with water due to phase inversion, polysulfonic microcapsules impregnated with the extractant were obtained, these microcapsules were immersed and stabilized in the water bath for 24 h

  3. Recovery of valuable metals from waste cathode materials of spent lithium-ion batteries using mild phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Xiangping, E-mail: chenxiangping101@163.com [School of Environmental Science and Engineering, Shaanxi University of Science & Technology, Xi’an 710021 (China); College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Ma, Hongrui, E-mail: mahr@sust.edu.cn [School of Environmental Science and Engineering, Shaanxi University of Science & Technology, Xi’an 710021 (China); Luo, Chuanbao; Zhou, Tao [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China)

    2017-03-15

    Graphical abstract: Cobalt can be directly recovered as Co{sub 3}(PO{sub 4}){sub 2} from waste LiCoO{sub 2} using H{sub 3}PO{sub 4} as leaching and precipitating agent. - Highlights: • Phosphoric acid was innovatively used as leaching and precipitating agent. • Over 99% Co and Li can be separated and recovered in a single leaching step. • Co and Li can be separated under mild conditions of 40 °C and 0.7 M H{sub 3}PO{sub 4}. • Activation energy values for Co and Li are 7.3 and 10.168 kJ/mol. • Cobalt phosphate (97.1% in purity) can be obtained as the leaching product. - Abstract: Sustainable recycling of valuable metals from spent lithium-ion batteries (LIBs) may be necessary to alleviate the depletion of strategic metal resources and potential risk of environmental pollution. Herein a hydrometallurgical process was proposed to explore the possibility for the recovery of valuable metals from the cathode materials (LiCoO{sub 2}) of spent LIBs using phosphoric acid as both leaching and precipitating agent under mild leaching conditions. According to the leaching results, over 99% Co can be separated and recovered as Co{sub 3}(PO{sub 4}){sub 2} in a short-cut process involved merely with leaching and filtrating, under the optimized leaching conditions of 40 °C (T), 60 min (t), 4 vol.% H{sub 2}O{sub 2}, 20 mL g{sup −1} (L/S) and 0.7 mol/L H{sub 3}PO{sub 4}. Then leaching kinetics was investigated based on the logarithmic rate kinetics model and the obtained results indicate that the leaching of Co and Li fits well with this model and the activation energies (Ea) for Co and Li are 7.3 and 10.2 kJ/mol, respectively. Finally, it can be discovered from characterization results that the obtained product is 97.1% pure cobalt phosphate (Co{sub 3}(PO{sub 4}){sub 2}).

  4. Effect of 4-(N,N-diethylamino)benzaldehyde thiosemicarbazone on the corrosion of aged 18 Ni 250 grade maraging steel in phosphoric acid solution

    International Nuclear Information System (INIS)

    Poornima, T.; Nayak, Jagannath; Nityananda Shetty, A.

    2011-01-01

    Highlights: → DEABT as corrosion inhibitor for maraging steel in phosphoric acid. → Inhibition efficiency increases with increase in inhibitor concentration. → Inhibition efficiency decreases with increase in temperature. → Adsorption obeys Langmuir adsorption isotherm. - Abstract: 4-(N,N-diethylamino)benzaldehyde thiosemicarbazone (DEABT) was studied for its corrosion inhibition property on the corrosion of aged 18 Ni 250 grade maraging steel in 0.67 M phosphoric acid at 30-50 deg. C by potentiodynamic polarization, EIS and weight loss techniques. Inhibition efficiency of DEABT was found to increase with the increase in DEABT concentration and decrease with the increase in temperature. The activation energy E a and other thermodynamic parameters (ΔG ads 0 , ΔH ads 0 , ΔS ads 0 ) have been evaluated and discussed. The adsorption of DEABT on aged maraging steel surface obeys the Langmuir adsorption isotherm model and the inhibitor showed mixed type inhibition behavior.

  5. COMPARATIVE STUDY OF THE SHEAR BOND STRENGTH OF COMPOSITE RESIN TO DENTAL ENAMEL CONDITIONED WITH PHOSPHORIC ACID OR Nd: YAG LASER

    Directory of Open Access Journals (Sweden)

    EDUARDO Carlos de Paula

    1997-01-01

    Full Text Available This study has been focused on a comparison between the shear bond strength of a composite resin attached to dental enamel surface, after a 35% phosphoric acid etching and after a Nd:YAG laser irradiation with 165.8 J/cm2 of energy density per pulse. After etching and attaching resin to these surfaces, the specimens were thermocycled and then underwent the shearing bond strength tests at a speed of 5 mm/min. The results achieved, after statistical analysis with Student's t-test, showed that the adhesion was significantly greater in the 35% phosphoric acid treated group than in the group treated with the Nd:YAG laser, thus demonstrating the need for developing new studies to reach the ideal parameters for an effective enamel surface conditioning as well as specific adhesives and composite resins when Nd:YAG laser is used

  6. Evaluation of efficient glucose release using sodium hydroxide and phosphoric acid as pretreating agents from the biomass of Sesbania grandiflora (L.) Pers.: A fast growing tree legume.

    Science.gov (United States)

    Mund, Nitesh K; Dash, Debabrata; Barik, Chitta R; Goud, Vaibhav V; Sahoo, Lingaraj; Mishra, Prasannajit; Nayak, Nihar R

    2017-07-01

    Sesbania grandiflora (L.) Pers. is one of the fast growing tree legumes having the efficiency to produce around 50tha -1 above ground dry matters in a year. In this study, biomass of 2years old S. grandiflora was selected for the chemical composition, pretreatments and enzymatic hydrolysis studies. The stem biomass with a wood density of 3.89±0.01gmcm -3 contains about 38% cellulose, 12% hemicellulose and 28% lignin. Enzymatic hydrolysis of pretreated biomass revealed that phosphoric acid (H 3 PO 4 ) pretreated samples even at lower cellulase loadings [1 Filter Paper Units (FPU)], could efficiently convert about 86% glucose, while, even at higher cellulase loadings (60FPU) alkali pretreated biomass could convert only about 58% glucose. The effectiveness of phosphoric acid pretreatment was also supported by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM) and Fourier transform infrared spectroscopy (FTIR) analysis. Copyright © 2017 Elsevier Ltd. All rights reserved.

  7. Research and development of a phosphoric acid fuel cell/battery power source integrated in a test-bed bus. Final report

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-05-30

    This project, the research and development of a phosphoric acid fuel cell/battery power source integrated into test-bed buses, began as a multi-phase U.S. Department of Energy (DOE) project in 1989. Phase I had a goal of developing two competing half-scale (25 kW) brassboard phosphoric acid fuel cell systems. An air-cooled and a liquid-cooled fuel cell system were developed and tested to verify the concept of using a fuel cell and a battery in a hybrid configuration wherein the fuel cell supplies the average power required for operating the vehicle and a battery supplies the `surge` or excess power required for acceleration and hill-climbing. Work done in Phase I determined that the liquid-cooled system offered higher efficiency.

  8. Comparison of arsenic acid with phosphoric acid in the interaction with a water molecule and an alkali/alkaline-earth metal cation.

    Science.gov (United States)

    Park, Sung Woo; Kim, Chang Woo; Lee, Ji Hyun; Shim, Giwoong; Kim, Kwang S

    2011-10-20

    Recently, Wolfe-Simon has discovered a bacterium which is able to survive using arsenic(V) rather than phosphorus(V) in its DNA. Thus it is important to investigate some important structural and chemical similarities and dissimilarities between phosphate and arsenate. We compared the monohydrated structures and the alkali/alkaline-earth metal (Na(+), K(+), Mg(2+) and Ca(2+)) complexes of the arsenic acid/anions with those of the phosphoric acid/anions [i.e., H(m)PO(4)(-(3-m)) vs H(m)AsO(4)(-(3-m)) (m = 1-3)]. We carried out geometry optimization along with harmonic frequency calculations using ab initio calculations. Despite the increased van der Waals radius of As, the hydrated structures of both P and As systems show very close similarity (within 0.25 Å in the P/As···O(water) distance and within a few kJ/mol in binding energy) because of the increased induction energies by more polar arsenic acid/anons and slightly increased dispersion energy by a larger size of the As atom. In the metal complexes, the arsenic acid has a slightly larger binding distance (by 0.07-1.0 Å) and weaker binding energy because the As(V) ion has a slightly larger radius than the P(V) ion, and the electrostatic interaction is the dominating feature in these systems.

  9. Influence of duration of phosphoric acid pre-etching on bond durability of universal adhesives and surface free-energy characteristics of enamel.

    Science.gov (United States)

    Tsujimoto, Akimasa; Barkmeier, Wayne W; Takamizawa, Toshiki; Watanabe, Hidehiko; Johnson, William W; Latta, Mark A; Miyazaki, Masashi

    2016-08-01

    The purpose of this study was to evaluate the influence of duration of phosphoric acid pre-etching on the bond durability of universal adhesives and the surface free-energy characteristics of enamel. Three universal adhesives and extracted human molars were used. Two no-pre-etching groups were prepared: ground enamel; and enamel after ultrasonic cleaning with distilled water for 30 s to remove the smear layer. Four pre-etching groups were prepared: enamel pre-etched with phosphoric acid for 3, 5, 10, and 15 s. Shear bond strength (SBS) values of universal adhesive after no thermal cycling and after 30,000 or 60,000 thermal cycles, and surface free-energy values of enamel surfaces, calculated from contact angle measurements, were determined. The specimens that had been pre-etched showed significantly higher SBS and surface free-energy values than the specimens that had not been pre-etched, regardless of the aging condition and adhesive type. The SBS and surface free-energy values did not increase for pre-etching times of longer than 3 s. There were no significant differences in SBS values and surface free-energy characteristics between the specimens with and without a smear layer. The results of this study suggest that phosphoric acid pre-etching of enamel improves the bond durability of universal adhesives and the surface free-energy characteristics of enamel, but these bonding properties do not increase for phosphoric acid pre-etching times of longer than 3 s. © 2016 Eur J Oral Sci.

  10. Regio-, Diastereo-, and Enantioselective Nitroso-Diels-Alder Reaction of 1,3-Diene-1-carbamates Catalyzed by Chiral Phosphoric Acids.

    Science.gov (United States)

    Pous, Jonathan; Courant, Thibaut; Bernadat, Guillaume; Iorga, Bogdan I; Blanchard, Florent; Masson, Géraldine

    2015-09-23

    Chiral phosphoric acid-catalyzed asymmetric nitroso-Diels-Alder reaction of nitrosoarenes with carbamate-dienes afforded cis-3,6-disubstituted dihydro-1,2-oxazines in high yields with excellent regio-, diastereo-, and enantioselectivities. Interestingly, we observed that the catalyst is able not only to control the enantioselectivity but also to reverse the regioselectivity of the noncatalyzed nitroso-Diels-Alder reaction. The regiochemistry reversal and asynchronous concerted mechanism were confirmed by DFT calculations.

  11. Anodic luminescence, structural, photoluminescent, and photocatalytic properties of anodic oxide films grown on niobium in phosphoric acid

    Energy Technology Data Exchange (ETDEWEB)

    Stojadinović, Stevan, E-mail: sstevan@ff.bg.ac.rs [University of Belgrade, Faculty of Physics, Studentski trg 12-16, 11000 Belgrade (Serbia); Tadić, Nenad [University of Belgrade, Faculty of Physics, Studentski trg 12-16, 11000 Belgrade (Serbia); Radić, Nenad [University of Belgrade, Institute of Chemistry, Technology and Metallurgy, Department of Catalysis and Chemical Engineering, Njegoševa 12, 11000 Belgrade (Serbia); Stefanov, Plamen [Institute of General and Inorganic Chemistry, Bulgarian Academy of Sciences, Acad. G. Bonchev Str., Block 11, 1113 Sofia (Bulgaria); Grbić, Boško [University of Belgrade, Institute of Chemistry, Technology and Metallurgy, Department of Catalysis and Chemical Engineering, Njegoševa 12, 11000 Belgrade (Serbia); Vasilić, Rastko [University of Belgrade, Faculty of Physics, Studentski trg 12-16, 11000 Belgrade (Serbia)

    2015-11-15

    Graphical abstract: - Highlights: • Anodic luminescence is correlated to the existence of morphological defects in the oxide. • Spectrum under spark discharging reveals only oxygen and hydrogen lines. • Oxide films formed under spark discharging are crystallized and composed of Nb{sub 2}O{sub 5}. • Photocatalytic activity and photoluminescence of Nb{sub 2}O{sub 5} films increase with time. - Abstract: This article reports on properties of oxide films obtained by anodization of niobium in phosphoric acid before and after the dielectric breakdown. Weak anodic luminescence of barrier oxide films formed during the anodization of niobium is correlated to the existence of morphological defects in the oxide layer. Small sized sparks generated by dielectric breakdown of formed oxide film cause rapid increase of luminescence intensity. The luminescence spectrum of obtained films on niobium under spark discharging is composed of continuum radiation and spectral lines caused by electronic spark discharging transitions in oxygen and hydrogen atoms. Oxide films formed before the breakdown are amorphous, while after the breakdown oxide films are partly crystalline and mainly composed of Nb{sub 2}O{sub 5} hexagonal phase. The photocatalytic activity of obtained oxide films after the breakdown was investigated by monitoring the degradation of methyl orange. Increase of the photocatalytic activity with time is related to an increase of oxygen vacancy defects in oxide films formed during the process. Also, higher concentration of oxygen vacancy defects in oxide films results in higher photoluminescence intensity.

  12. Maximum power output and load matching of a phosphoric acid fuel cell-thermoelectric generator hybrid system

    Science.gov (United States)

    Chen, Xiaohang; Wang, Yuan; Cai, Ling; Zhou, Yinghui

    2015-10-01

    Based on the current models of phosphoric acid fuel cells (PAFCs) and thermoelectric generators (TGs), a new hybrid system is proposed, in which the effects of multi-irreversibilities resulting from the activation, concentration, and ohmic overpotentials in the PAFC, Joule heat and heat leak in the TG, finite-rate heat transfer between the TG and the heat reservoirs, and heat leak from the PAFC to the environment are taken into account. Expressions for the power output and efficiency of the PAFC, TG, and hybrid system are analytically derived and directly used to discuss the performance characteristics of the hybrid system. The optimal relationship between the electric currents in the PAFC and TG is obtained. The maximum power output is numerically calculated. It is found that the maximum power output density of the hybrid system will increase about 150 Wm-2, compared with that of a single PAFC. The problem how to optimally match the load resistances of two subsystems is discussed. Some significant results for practical hybrid systems are obtained.

  13. Optimizing Phosphoric Acid plus Hydrogen Peroxide (PHP) Pretreatment on Wheat Straw by Response Surface Method for Enzymatic Saccharification.

    Science.gov (United States)

    Qiu, Jingwen; Wang, Qing; Shen, Fei; Yang, Gang; Zhang, Yanzong; Deng, Shihuai; Zhang, Jing; Zeng, Yongmei; Song, Chun

    2017-03-01

    Wheat straw was pretreated by phosphoric acid plus hydrogen peroxide (PHP), in which temperature, time, and H 3 PO 4 proportion for pretreatment were investigated by using response surface method. Results indicated that hemicellulose and lignin removal positively responded to the increase of pretreatment temperature, H 3 PO 4 proportion, and time. H 3 PO 4 proportion was the most important variable to control cellulose recovery, followed by pretreatment temperature and time. Moreover, these three variables all negatively related to cellulose recovery. Increasing H 3 PO 4 proportion can improve enzymatic hydrolysis; however, reduction on cellulose recovery results in decrease of glucose yield. Extra high temperature or long time for pretreatment was not beneficial to enzymatic hydrolysis and glucose yield. Based on the criterion for minimizing H 3 PO 4 usage and maximizing glucose yield, the optimized pretreatment conditions was 40 °C, 2.0 h, and H 3 PO 4 proportion of 70.2 % (H 2 O 2 proportion of 5.2 %), by which glucose yielded 299 mg/g wheat straw (946.2 mg/g cellulose) after 72-h enzymatic hydrolysis.

  14. (Liquid + liquid) equilibrium data of (water + phosphoric acid + solvents) systems at T = (308.2 and 318.2) K

    International Nuclear Information System (INIS)

    Ghanadzadeh Gilani, H.; Ghanadzadeh Gilani, A.; Shekarsaraee, S.; Uslu, H.

    2012-01-01

    Highlights: ► Phase equilibria of the (water + PA + solvents) systems were investigated. ► Experimental LLE data were correlated with NRTL and UNIQUAC models. ► Distribution coefficients and separation factors were evaluated. - Abstract: Ternary equilibrium data for the mixtures of {water + phosphoric acid + organic solvent (cyclohexane, methylcyclohexane, and toluene)} were determined at T = (308.2 and 318.2) K and atmospheric pressure. Solubility data were determined by the cloud-point titration method. In order to obtain the tie-line data, the concentration of each phase was determined by acidimetric titration, the Karl–Fischer technique, and refractive index measurements. The experimental tie-line data were correlated using the UNIQUAC and NRTL models. The reliability of the experimental data was determined through the Othmer–Tobias and Hand plots. Distribution coefficients and separation factors were evaluated over the immiscibility regions. The Katritzky LSER model was applied to correlate distribution coefficients and separation factors in these ternary systems.

  15. Comparison of 2-Octanol and Tributyl Phosphate in Recovery of Tungsten from Sulfuric-Phosphoric Acid Leach Solution of Scheelite

    Science.gov (United States)

    Liao, Yulong; Zhao, Zhongwei

    2018-04-01

    Tungsten was recovered from sulfuric-phosphoric acid leach solution of scheelite using 2-octanol and tributyl phosphate (TBP). Approximately 76% of the tungsten and less than 6.2% of the iron were extracted when using 70% 2-octanol, showing good selectivity for tungsten over iron; the tungsten extraction could not be significantly enhanced using a three-stage countercurrent simulation test. Moreover, more than 99.2% of the W and 91.0% of the Fe were extracted when using 70% TBP, showing poor selectivity, but after pretreating the leach solution with iron powder, less than 5.5% of the Fe was extracted. The loaded phases were stripped using deionized water and ammonia solution. The maximum stripping rate of tungsten from loaded 2-octanol was 45.6% when using water, compared with only 13.1% from loaded TBP. Tungsten was efficiently stripped from loaded phases using ammonia solution without formation of Fe(OH)3 precipitate. Finally, a flow sheet for recovery of tungsten with TBP is proposed.

  16. Some aromatic hydrazone derivatives as inhibitors for the corrosion of C-steel in phosphoric acid solution.

    Science.gov (United States)

    Fouda, Abd El-Aziz S; Al-Sarawy, Ahmed A; Radwan, Mohamed S

    2006-01-01

    The effect of furfural benzoylhydrazone and its derivatives (I-VII) as corrosion inhibitors for C-steel in 1M phosphoric acid solution has been studied by weight-loss and galvanostatic polarization techniques. A significant decrease in the corrosion rate of C-steel was observed in the presence of the investigated inhibitors. This study revealed that, the inhibition efficiency increases with increasing the inhibitor concentration, and the addition of iodide ions enhances it to a considerable extent. The effect of temperature on the inhibition efficiency of these compounds was studied using weight-loss method. Activation energy (E(a)*) and other thermodynamic parameters for the corrosion process were calculated and discussed. The galvanostatic polarization data indicated that, the inhibitors were of mixed-type, but the cathode is more polarized than the anode. The adsorption of these compounds on C-steel surface has been found to obey Frumkin's adsorption isotherm. The mechanism of inhibition was discussed in the light of the chemical structure of the undertaken inhibitors.

  17. High temperature dilute phosphoric acid pretreatment of corn stover for furfural and ethanol production

    Science.gov (United States)

    Furfural was produced from corn stover by one stage pretreatment process using dilute H3PO4 and solid residues following furfural production were used for ethanol production by Saccharomyces cerevisiae NRRL- Y2034. A series of experiments were conducted at varied temperatures (140-200 oC) and acid ...

  18. Kinetic study of the precipitation of radioactive elements in the production process of phosphoric acid

    International Nuclear Information System (INIS)

    Ben Mahmoud, Souha

    2009-01-01

    In this engineering study we determined the activities of gamma emitting radionuclides belonging to the families of 238 U , 232 Th and 40K in phosphate, the acid derivatives and gypsum in Tunisian Chemical Group. The most important activities are those of 238 U and 226 Ra, which are located in the phosphate, gypsum and the precipitates formed in the pipes.

  19. Liquid crystalline solutions of cellulose in phosphoric acid for preparing cellulose yarns

    NARCIS (Netherlands)

    Boerstoel, H.

    2006-01-01

    The presen thesis describes a new process for manufacturing high tenacity and high modulus cellulose yarns. A new direct solvent for cellulose has been discovered, leading to liquid crystalline solutions. This new solvent, superphosphoric acid, rapidly dissolves cellulose. These liquid crystalline

  20. Tensile bond strength and SEM analysis of enamel etched with Er:YAG laser and phosphoric acid: a comparative study in vitro

    International Nuclear Information System (INIS)

    Sasaki, Luis H.; Tanaka, Celso Shin-Ite; Lobo, Paulo D.C.; Villaverde, Antonio B.; Moriyama, Eduardo H.; Brugnera Junior, Aldo; Moriyama, Yumi; Watanabe, Ii-Sei

    2008-01-01

    Er:YAG laser has been studied as a potential tool for restorative dentistry due to its ability to selectively remove oral hard tissue with minimal or no thermal damage to the surrounding tissues. The purpose of this study was to evaluate in vitro the tensile bond strength (TBS) of an adhesive/composite resin system to human enamel surfaces treated with 37% phosphoric acid, Er:YAG laser (λ=2.94 μm) with a total energy of 16 J (80 mJ/pulse, 2Hz, 200 pulses, 250 ms pulse width), and Er:YAG laser followed by phosphoric acid etching. Analysis of the treated surfaces was performed by scanning electron microscopy (SEM) to assess morphological differences among the groups. TBS means (in MPa) were as follows: Er:YAG laser + acid (11.7 MPa) > acid (8.2 MPa) > Er:YAG laser (6.1 MPa), with the group treated with laser+acid being significantly from the other groups (p=0.0006 and p= 0.00019, respectively). The groups treated with acid alone and laser alone were significantly different from each other (p=0.0003). The SEM analysis revealed morphological changes that corroborate the TBS results, suggesting that the differences in TBS means among the groups are related to the different etching patterns produced by each type of surface treatment. The findings of this study indicate that the association between Er:YAG laser and phosphoric acid can be used as a valuable resource to increase bond strength to laser-prepared enamel. (author)

  1. Electrochemistry of carbonaceous materials; 2. Anodic electroactivity of coal slurries in 85% phosphoric acid media

    Energy Technology Data Exchange (ETDEWEB)

    Tomat, R.; Salmaso, R.; Zecchin, S. (CNR-Instituto di Polarografia ed Elettrochimica Preparative, Padova (Italy))

    1992-04-01

    Current-potential curves of suspended coal (Sulcis basin, Sardinia, Italy) in 85% H{sub 3}PO{sub 4} were taken on a platinum electrode at 100{degree}C. Anodic current in the potential range of 0-1.5 V versus saturated calomel electrode was due to some humic acid-type substances released by coal in the electrolyte. The leaching of organic matter increased with the lowering of the particle dimensions, and the related oxidation currents attained stable values even during slurry formation. Current-potential curves were still unchanged when coal was filtered off from the suspension. Previous washing of ground coal with diluted mineral acids, including H{sub 3}PO{sub 4}, did not dissolve any significant amount of the substances responsible for the electrochemical activity of the coal sample examined. 14 refs., 6 figs.

  2. Phase distribution of ecologically controlled chemical elements in production of extraction phosphoric acid

    International Nuclear Information System (INIS)

    Kazak, V.G.; Agnelov, A.I.; Zajtsev, P.M.

    1995-01-01

    Content of 16 ecologically controlled chemical element (among them Cd, Sr, Th, U, V, Y) in solid and liquid phases of extraction phosphorus acid (EPA) production is determined. These elements are recommended to control by Scientific research institute of human ecology and environment to establish their extraction coefficients to phosphogypsum and EPA and optimal variant of production of ecologically sate phosphorus fertilizers. X-ray fluorescent, atomic-absorption and polarographic methods are used for analysis these elements

  3. Determination of specific activity of phosphorus-32 labelled o-phosphoric acid

    International Nuclear Information System (INIS)

    Sane, S.U.

    2015-01-01

    Phosphorus-32 is one of the important radioisotopes used in therapeutic nuclear medicine. This work was aimed at developing a fast and sensitive procedure to determine trace amounts of 32 P which is present in various acidic chemical form thereby enabling to determine its specific activity. The method utilizes ammonium molybdate and metol for complexing with phosphorus in presence of sulphuric acid which was measured using UV-VIS spectrophotometer. The phosphate and molybdate ions form a stable complex which turns blue (molybdenum blue) by reduction with sulphuric acid. The absorbance of the complex thus formed was measured at 700 nm. Five batches of 32 P produced were analyzed using the procedure and specific activity was determined. It was found that radioactivity of 32 P did not interfere in absorbance measurements and the method could be successfully adopted for the determination of specific activity of 32 P. A scope of the method is to find the chemical purity of radioactive phosphorus ( 32 P) in quality control analysis. (author)

  4. A new oxidimetric reagent: potassium dichromate in a strong phosphoric acid medium-VI Potentiometric titration of vanadium(III) alone and in mixture with vanadium(IV).

    Science.gov (United States)

    Rao, G G; Rao, P K

    1966-09-01

    Vanadium(III) can be titrated at room temperature with potassium dichromate in an 8-12M phosphoric acid medium. Two potential breaks are observed in 12M phosphoric add with 0.2N potassium dichromate, the first corresponding to the oxidation of vanadium(III) to vanadium(IV) and the second to the oxidation of vanadium(IV) to vanadium(V). In titrations with 0.05N dichromate only the first break in potential is clearly observed. The method has been extended to the titration of mixtures of vanadium(III) and vanadium(IV). Conditions have also been found for the visual titration of vanadium(III) using ferroln or barium diphenylamine sulphonate as indicator.

  5. Determination of the O/M ratios of polynary uranium oxides by Ce(IV)-Fe(II) back titration after dissolution in mixed sulphuric and phosphoric acids

    International Nuclear Information System (INIS)

    Fujino, T.; Sato, N.; Yamada, K.

    1996-01-01

    Uranium (IV) in polynary uranium oxides is determined after the solid has been dissolved in a warm mixed solution of sulphuric and phosphoric acids containing excess Ce(IV). The latter is titrated with a Fe(II) standard solution using ferroin as indicator. This method is especially effective for (mixed) uranium oxides which are difficult to dissolve in hot Ce(IV) sulphuric acid. The standard deviation of the determined x value in polynary oxides is estimated to be below ± 0.004 for samples of 10-30 mg. (orig.)

  6. Determination of the O/M ratios of polynary uranium oxides by Ce(IV)-Fe(II) back titration after dissolution in mixed sulphuric and phosphoric acids.

    Science.gov (United States)

    Fujino, T; Sato, N; Yamada, K

    1996-01-01

    Uranium (IV) in polynary uranium oxides is determined after the solid has been dissolved in a warm mixed solution of sulphuric and phosphoric acids containing excess Ce(IV). The latter is titrated with a Fe(II) standard solution using ferroin as indicator. This method is especially effective for (mixed) uranium oxides which are difficult to dissolve in hot Ce(IV) sulphuric acid. The standard deviation of the determined x value in polynary oxides is estimated to be below +/- 0.004 for samples of 10-30 mg.

  7. Development of a volumetric Analysis method to determine uranium in the loaded phosphoric acid and the loaded organic phase (DEHPA/TOPO)

    International Nuclear Information System (INIS)

    Shlewit, H.; Koudsi, Y.

    2003-01-01

    Rapid and reliable volumetric analysis method has been developed to determine uranium, on line, at uranium extraction unit from wet-process phosphoric acid, in aqueous and organic phases. This process enable up 300 mg of uranium to be determined in the presence of nitric acid, in a sample volume of up to at least 10 ml. The volume of the sample, the amounts of reagents added, the temperature of the reagents and the standing time of various stages were investigated to ensure that the conditions selected for the final procedure were reasonably non-critical

  8. SORPTION OF CESIUM USING KZnFc ON PHOSPHORIC ACID-BASED GEOPOLYMER

    Directory of Open Access Journals (Sweden)

    Li-Ching Chuang

    2015-06-01

    Full Text Available The adsorbent was synthesized from the acid-base reaction between metal ferrocyanide and acidic phosphate at room temperature. The metal ferrocyanide granular inorganic adsorbent based on phosphate geopolymer for the removal of cesium in either batch or packed-bed operation has been developed in this study. In this work, the compressive strength of granular inorganic adsorbent was investigated under different liquid-to-solid, metal ferrocyanide-to-geopolymer and MgO-to-KH2PO4 ratios. The result showed that the compressive strength of the adsorbent increased with the increase of MgO-to- KH2PO4 ratio. It was found that the optimization of metal ferrocyanide-to-geopolymer and MgO-to- KH2PO4 ratios was important in improving both the compressive strength and the adsorption capacity of the adsorbent. The metal ferrocyanide granular inorganic adsorbent prepared were characterized by analysis such as XRD, TGA, FTIR and SEM spectra. In this study, the synthesized granular inorganic adsorbent has demonstrated a Cs removal efficiency of over 99 % and an adsorption capacity of 1.7-1.8 meq.g-1 in simulation wastewater containing 2000 ppm Cs under adsorbent dose of 0.0067 g.ml-1.

  9. Phosphoric acid doped polybenzimidazole membranes: Physiochemical characterization and fuel cell applications [PEM fuel cells

    DEFF Research Database (Denmark)

    Qingfeng, Li; Hjuler, Hans Aage; Bjerrum, Niels

    2001-01-01

    A polymer electrolyte membrane fuel cell operational at temperatures around 150-200 degrees C is desirable for fast electrode kinetics and high tolerance to fuel impurities. For this purpose polybenzimidazole (PBI) membranes have been prepared and H/sub 3/PO/sub 4/-doped in a doping range from 300...... doping level. At 160 degrees C a conductivity as high as 0.13 S cm/sup -1/ is obtained for membranes of high doping levels. Mechanical strength measurements show, however, that a high acid doping level results in poor mechanical properties. At operational temperatures up to 190 degrees C, fuel cells...... based on this polymer membrane have been tested with both hydrogen and hydrogen containing carbon monoxide....

  10. Separation and accumulation of acitinides with the aid of a phosphoric acid polymer

    International Nuclear Information System (INIS)

    Novikov, A.; Geckeler, K.E.

    1993-01-01

    A new method for the separation and enrichment of actinides based on the use of polymer reagents is presented, in this study, poly(ethyleneimine methylphosphonic acid) was used for the interaction with actinide ions in the homogeneous phase. In conjunction with membrane filtration this reagent allows both the separation and the enrichment of actinides from dilute solutions. The retention profiles for the series of actinides U(VI), Np(V), Pu(IV), Am(III), Cm(III), Cf(III) were investigated at different pH. Retention differences between 0% and 100% were found depending on the actinide element and pH. Thus, these elements can be separated and enriched form aqueous solutions of binary or multi-component mixtures. (orig.)

  11. Physicochemical properties of phosphoric acid doped polybenzimidazole membranes for fuel cells

    DEFF Research Database (Denmark)

    He, Ronghuan; Li, Qingfeng; Bach, Anders

    2006-01-01

    of the polymer, a level necessary to obtain high enough proton conductivity for fuel cell uses, the polymer membrane exhibits a volume swelling by 118%, resulting in separation of the polymer backbones. The separation in turn reduces the mechanical strength of the membrane especially at high temperatures....... Another consequence is the increased H2 and O2 permeability through the membrane. In the temperature range from 120 to 180 ◦C, the hydrogen permeability was found to be 1.6–4.3×10−17 and 1.2–4.0×10−15 mol cm cm−2 s−1 Pa−1 for pristine and acid doped PBI membranes, respectively, while for oxygen it was 5...

  12. Assessment of activated carbon prepared from corncob by chemical activation with phosphoric acid

    Directory of Open Access Journals (Sweden)

    Gamal O. El-Sayed

    2014-09-01

    Full Text Available Corncob, which is the main waste from corn agricultures in Egypt, has been used as a raw material for the preparation of different activated carbons. Activated carbons (ACs were prepared by chemical activation with concentrated H3PO4 acid; followed by pyrolysis at 400, 500 and 600 °C. Different ACs have been used for the removal of methylene blue (MB dye from aqueous solutions. Batch adsorption experiments were performed as a function of initial dye concentration, contact time, adsorbent dose and pH. Adsorption data were modeled using the Langmuir and Freundlich adsorption isotherms. Adsorption of MB on AC1 (R2=0.9868 and AC2 (R2=0.9810 followed Langmuir model with maximum monolayer sorption capacity of 28.65 and 17.57 mg/g, respectively. Adsorption onto AC3 was better fitted to Freundlich isotherm model (R2=0.9823.

  13. Environmental, health, and safety issues of fuel cells in transportation. Volume 1: Phosphoric acid fuel-cell buses

    Energy Technology Data Exchange (ETDEWEB)

    Ring, S

    1994-12-01

    The U.S. Department of Energy (DOE) chartered the Phosphoric Acid Fuel-Cell (PAFC) Bus Program to demonstrate the feasibility of fuel cells in heavy-duty transportation systems. As part of this program, PAFC- powered buses are being built to meet transit industry design and performance standards. Test-bed bus-1 (TBB-1) was designed in 1993 and integrated in March 1994. TBB-2 and TBB-3 are under construction and should be integrated in early 1995. In 1987 Phase I of the program began with the development and testing of two conceptual system designs- liquid- and air-cooled systems. The liquid-cooled PAFC system was chosen to continue, through a competitive award, into Phase H, beginning in 1991. Three hybrid buses, which combine fuel-cell and battery technologies, were designed during Phase III. After completing Phase II, DOE plans a comprehensive performance testing program (Phase HI) to verify that the buses meet stringent transit industry requirements. The Phase III study will evaluate the PAFC bus and compare it to a conventional diesel bus. This NREL study assesses the environmental, health, and safety (EH&S) issues that may affect the commercialization of the PAFC bus. Because safety is a critical factor for consumer acceptance of new transportation-based technologies the study focuses on these issues. The study examines health and safety together because they are integrally related. In addition, this report briefly discusses two environmental issues that are of concern to the Environmental Protection Agency (EPA). The first issue involves a surge battery used by the PAFC bus that contains hazardous constituents. The second issue concerns the regulated air emissions produced during operation of the PAFC bus.

  14. Luminescence resonance energy transfer-based nucleic acid hybridization assay on cellulose paper with upconverting phosphor as donors.

    Science.gov (United States)

    Zhou, Feng; Noor, M Omair; Krull, Ulrich J

    2014-03-04

    A bioassay based on DNA hybridization on cellulose paper is a promising format for gene fragment detection that may be suited for in-field and rapid diagnostic applications. We demonstrate for the first time that luminescence resonance energy transfer (LRET) associated with upconverting phosphors (UCPs) can be used to develop a paper-based DNA hybridization assay with high sensitivity, selectivity and fast response. UCPs with strong green emission were synthesized and subsequently functionalized with streptavidin (UCP-strep). UCP-strep particles were immobilized on cellulose paper, and then biotinylated single-stranded oligonucleotide probes were conjugated onto the UCPs via streptavidin-biotin linkage. The UCPs served as donors that were LRET-paired with Cy3-labeled target DNA. Selective DNA hybridization enabled the proximity required for LRET-sensitized emission from Cy3, which was used as the detection signal. Hybridization was complete within 2 min, and the limit of detection of the method was 34 fmol, which is a significant improvement in comparison to an analogous fluorescence resonance energy transfer (FRET) assay based on quantum dots. The assay exhibited excellent resistance to nonspecific adsorption of noncomplementary short/long DNA and protein. The selectivity of the assay was further evaluated by one base pair mismatched (1BPM) DNA detection, where a maximum signal ratio of 3.1:1 was achieved between fully complementary and 1BPM samples. This work represents a preliminary but significant step for the development of paper-based UCP-LRET nucleic acid hybridization assays, which offer potential for lowering the limit of detection of luminescent hybridization assays due to the negligible background signal associated with optical excitation by near-infrared (NIR) light.

  15. Surface decoration of polyimide fiber with carbon nanotubes and its application for mechanical enhancement of phosphoric acid-based geopolymers

    Science.gov (United States)

    Yang, Tao; Han, Enlin; Wang, Xiaodong; Wu, Dezhen

    2017-09-01

    A new methodology to decorate the surface of polyimide (PI) fiber with carbon nanotubes (CNTs) has been developed in this study. This surface decoration was carried out through a surface alkali treatment, a carboxylation modification, surface functionalization with acyl chloride groups and then with amino groups, and a surface graft of CNTs onto PI fiber. Fourier-transform infrared and X-ray photoelectron spectroscopic characterizations confirmed that CNTs were chemically grafted onto the surface of PI fiber, and scanning electron microscopic observation demonstrated the fiber surface was uniformly and densely covered with CNTs. The surface energy and wettability of PI fiber were improved in the presence of CNTs on the fiber surface, which made a contribution to enhance the interfacial adhesion of PI fiber with other inorganic matrices when used as a reinforcing fiber. The application of CNTs-decorated PI fiber for the reinforcement of phosphoric acid-based geopolymers was investigated, and the results indicated that the geopolymeric composites gained a noticeable reinforcement. Compared to unreinforced geopolymer, the geopolymeric composites achieved a remarkable increase in compressive strength by 120% and in flexural strength by 283%. Fractography investigation demonstrated that the interaction adhesion between the fibers and matrix was enhanced due to the surface decoration of PI fiber with CNTs, which contributed to an improvement in fracture-energy dissipation by fiber pullout and fiber debonding from the matrix. As a result, a significant reinforcement effect on geopolymeric composites was achieved through a fiber-bridging mechanism. This study provided an effective methodology to improve the interracial bonding force for PI fiber and also proves a highly efficient application of CNTs-decorated PI fiber for the mechanical enhancement of geopolymeric composites.

  16. Study of the interference of uranium, vanadium, aluminium and molebdenum in the determination of FeII, FeIII in Syrian phosphoric acid by spectrophotometry

    International Nuclear Information System (INIS)

    Zaizafoun, Ghadir; Elian, Nazha

    1991-04-01

    The spectrophotometric determination of the ratio of iron I I to iron I II in crude phosphoric acid is of great importance because of its influence on the redox potential in the different stages which lead to the extraction of uranium from crude phosphoric acid. The suitability of a number of reagents for this determination was examined and only 1,10-phenanthroline, 5-sulfosalicylic acid and 2,2'-bipyridine were selected for further experimentation. 1-10-phenanthroline can give a deep red complex with Fe I I, in phosphoric acid medium at PH 4-6, absorbs at λ = 510 nm. The total iron was determined by reducing Fe I II to Fe I I using hydroxylamine hydrochloride. The second reagent was found capable of forming a yellow complex absorbs light at λ = 430 nm in amonia medium at PH 8.5 - 11 with Fe I II. The adopted procedure was to determine total iron first by oxidation with nitric acid. Then iron I I was determined in a second test at PH 1.5 and at λ = 500 nm. The third reagent i.e. 2-2' bipyridine is capable of forming a red complex with iron I I absorbs at λ = 522 nm. The interference of U, V, Al, and Mo was investigated. These elements were selected because of their presence in considerable amounts in Syrian commercial phosphoric acid. The work was designed so that the effect of the presence of each element as well as the presence of all possible combinations of these elements can be estimated. The investigation revealed that the interference is very high in the case of 2-2' bipyridine in addition to the instability of the complex. In the case of 1,10-phenanthroline the interference was also found high. Thus these two reagents were disregarded. The 5-sulfosalicylic reagent was found satisfactory when determining iron I II, However when Fe I I is considered the error resulting from interference ranges between 17.5 - 50%. This error was found very dependent on the PH of the medium and further work is in progress in order to lower the value of interferences

  17. Recovery of uranium from different acidic solutions by di-nonyl phenyl phosphoric acid (DNPPA) and TOPO

    International Nuclear Information System (INIS)

    Mishra, S.L.; Vijayalakshmi, R.; Singh, H.

    2004-01-01

    The extraction mechanism of uranium with DNPPA in combination with TOPO has been established from different acidic media. The extraction order of uranium from these media has been found as perchlorate>nitrate>chloride>sulphate>phosphate. Based on these results extraction of uranium from samples of leach liquors generated in the plant has been carried out and >99% recovery was obtained

  18. Separation and concentration of uranium by extraction chromatography : U(VI) - H3PO4 system

    International Nuclear Information System (INIS)

    Nobre, J.S.M.

    1981-01-01

    The feasibility of using the extraction chromatographic technique as a way to recover uranium from phosphatic rocks evaluated. The behaviour of uranium from raw phsophoric acid solutions in chromatographic systems using the mixture di(2-ethylhexyl) orthophosphoric acid (D2EHPA) - tributyl phosphate (TBP) as the stationary phase was studied. Materials as alumina, activated carbon and the macroporous resins XAD-4 and XAD-7 were used as supports for organic stationary phase. The best results were obtained with poliacrilic polymer XAD-7, due to its excellent chromatographic properties and efficient organic phase retention. Uranium was quantitatively retained by D2EHPA-TBP-XAD-7 columns from synthetic phosphoric acid solutions with typical composition of phosphatic acid liquors. The elution of uranium from this system was also studied, and the best results were obtained with phosphoric acid solutions. This chromatographic column presented a high stability, not changing their properties even after more than twenty cycles, including the conditioning, sorption, wasking and elution steps. Uranium determinations were perfpormed by indirect titration with potassium dichromate and by molecular absorption spectrophotometry with hydrogen peroxide- carbonate. A new and more sensitive method for uranium determination in phosphoric medium, which might be applied to acid liquors of phosphatic ores, was developed. An extraction-photometric method was used, with Arsenazo III (1,8-dihydroxynaphtalene-3,6-disulphonic acid-2,7-bis(azo-2)-phenylarsonic acid) as the reagent for uranium. (Author) [pt

  19. Separation and concentration of uranium by extraction chromatography : U(VI) - H/sub 3/PO/sub 4/ system

    Energy Technology Data Exchange (ETDEWEB)

    Nobre, J S.M.

    1981-01-01

    The feasibility of using the extraction chromatographic technique as a way to recover uranium from phosphatic rocks is evaluated. The behaviour of uranium from raw phsophoric acid solutions in chromatographic systems using the mixture di(2-ethylhexyl) orthophosphoric acid (D2EHPA) - tributyl phosphate (TBP) as the stationary phase was studied. Materials as alumina, activated carbon and the macroporous resins XAD-4 and XAD-7 were used as supports for organic stationary phase. The best results were obtained with poliacrilic polymer XAD-7, due to its excellent chromatographic properties and efficient organic phase retention. Uranium was quantitatively retained by D2EHPA-TBP-XAD-7 columns from synthetic phosphoric acid solutions with typical composition of phosphatic acid liquors. The elution of uranium from this system was also studied, and the best results were obtained with phosphoric acid solutions. This chromatographic column presented a high stability, not changing their properties even after more than twenty cycles, including the conditioning, sorption, washing and elution steps. Uranium determinations were perfpormed by indirect titration with potassium dichromate and by molecular absorption spectrophotometry with hydrogen peroxide- carbonate. A new and more sensitive method for uranium determination in phosphoric medium, which might be applied to acid liquors of phosphatic ores, was developed. An extraction-photometric method was used, with Arsenazo III (1,8-dihydroxynaphtalene-3,6-disulphonic acid-2,7-bis(azo-2)-phenylarsonic acid) as the reagent for uranium.

  20. Complexes of Cd sup 2 sup +, U(O sub 2 ) sup 2 sup + and Th sup 4 sup + at radiotracer levels with phosphoric acid

    International Nuclear Information System (INIS)

    Bouhlassa, S.; El-Yahyaoui, A.; Brillard, L.; Hussonnois, M.; Guillaumont, R.

    1994-01-01

    In this work, we have turn to account the radiochemical techniques in order to investigate the complexation of Cd sup 2 sup +, U(O sub 2) sup 2 sup + and Th sup 2 sup +, at strength Mu=0,2, in various phosphoric media characterized by C sub ( H sub 3 P O sub 4) <= 4 M and 0.7 <= pH <= 4. The method chosen for this purpose is the liquid-liquid extraction of radioisotopes at tracer scale, with di(2-ethyl hexyl) phosphoric acid dissolved in benzene. The radionuclides used are Cd-109, U-233, U-230 and Th-227. Their distribution between the two phases are established by alpha or gamma spectrometric analysis. The analysis of the distribution data allows to define, in addition of species extracted in organic phase, the nature of phosphoric complexes which take place in aqueous media. Stability constants of these complexes and associated thermodynamic data are determined. 2 tabs.; 2 refs. (author)

  1. Comparative evaluation of self-etching primers and phosphoric acid effectiveness on composite to enamel bond: an in vitro study.

    Science.gov (United States)

    Patil, Basanagouda S; Rao, Bk Raghavendra; Sharathchandra, Sm; Hegde, Reshma; Kumar, G Vinay

    2013-09-01

    The aim of the present study was to investigate the effectiveness of the one total-etch self-priming adhesive, one two-step self-etching primer adhesive, and one 'all-in-one' self-etching adhesive system on the adhesion of a resin composite to enamel. Thirty-six freshly extracted human mandibular molars were selected for this study. A fat area about 5 mm in diameter was created on the exposed mesial surface of enamel of each tooth by moist grinding with 320, 420 and 600 grit silicon carbide paper. Twelve teeth were randomly assigned into three groups. In group 1, Adper Easy One (3M ESPE), a one step self-etching primer adhesive was applied and light curing unit for 10 seconds. In group 2, Adper SE Plus, a two-step self-etching primer with bottle A containing the aqueous primer and bottle B containing the acidic adhesive was applied and light cured for 10 seconds. Group 3 (control)-etchant 37% phosphoric acid is applied to the surface for 15 seconds and rinsed with water and air dried and adhesive (single bond 2) is applied to the surface and tube is placed and light cured for 20 seconds. Composite material (Z350) was placed in the tube and light cured for 40 seconds in all the groups. Bond strength testing was done using universal testing machine at the enamel-composite interface. The debonded enamel surface was evaluated in stereomicroscope to assess the cohesive, adhesive or mixed fracture. Data was statistically analyzed by one way analysis of variance (ANOVA). Group 1 performed least among all groups with a mean score of 19.46 MPa. Group 2 had a mean score of 25.67 MPa. Group 3 had a mean score of 27.16 MPa. Under the conditions of this in vitro study, the bond strength values of the two-step self-etching primer systems tested were similar to the total-etch. And, one step self-etching primers have lower bond strength compared to the total-etch.

  2. Study of the solubility of yttrium, praseodymium, neodymium, and gadolinium sulfates in the presence of sodium and potassium in sulfuric-phosphoric acid solutions at 20 deg C

    International Nuclear Information System (INIS)

    Lokshin, Eh.P.; Tareeva, O.A.; Kashulina, T.G.

    2007-01-01

    The solubility of yttrium, praseodymium, neodymium, and gadolinium sulfates in the presence of sodium and potassium ions and the composition of solid phases were studied at 20 deg C in relation to the concentration of acids in sulfuric acid, phosphoric acid, and sulfuric-phosphoric acid solutions containing up to 36 wt % H 2 SO 4 and 33.12 g 1 -1 H 3 PO 4 . The formation of double sulfates of praseodymium and neodymium with sodium and potassium ions, as well as of gadolinium sulfate with sodium ions of the composition 1 : 1 was revealed. In water at 20 deg C, the solubility products of PrNa(SO 4 ) 2 ·H 2 O, NdNa(SO 4 ) 2 ·H 2 O, GdNa(SO 4 ) 2 ·H 2 O, PrK(SO 4 ) 2 ·H 2 O, and NdK(SO 4 ) 2 ·H 2 O are found to be 7.28x10 -8 , 7.84x10 -8 , 3.09x10 -6 , 3.02x10 -6 , and 1.70x10 -6 , respectively [ru

  3. A new oxidimetric reagent: potassium dichromate in a strong phosphoric acid medium--VII. Photometric titration of vanadium(IV) and of cerium(III) alone and in mixtures with iroN(II).

    Science.gov (United States)

    Rao, G G; Rao, P K

    1967-01-01

    Vanadium(IV) can be accurately titrated with potassium dichromate in media containing phosphoric acid of 3-12M concentration: the change in absorption of vanadium(IV) is followed in the region 660 mmicro using a red filter. It is more convenient to carry out the titration in 3M phosphoric acid because at higher concentrations chloride, nitrate, cerium(III) and manganese(II) may interfere. Photoelcetric titration is more convenient than potentiometric because the former can be made in a 3M phosphoric acid medium, whereas the latter is possible only in 12M phosphoric acid. The simultaneous differential photometric titration of iron(II) and vanadium(IV) is also possible. Conditions have been found for the photometric titration of cerium(III) and of cerium(III) plus iron(II). The titration is carried out (at 450 mmicro or with a blue filter) in about 10.5M phosphoric acid. Application of the method to a cerium mineral is considered.

  4. Phosphoric acid doped membranes based on Nafion®, PBI and their blends – Membrane preparation, characterization and steam electrolysis testing

    DEFF Research Database (Denmark)

    Aili, David; Hansen, Martin Kalmar; Pan, Chao

    2011-01-01

    Proton exchange membrane steam electrolysis at temperatures above 100 °C has several advantages from thermodynamic, kinetic and engineering points of view. A key material for this technology is the high temperature proton exchange membrane. In this work a novel procedure for preparation of Nafion......® and polybenzimidazole blend membranes was developed. Homogeneous binary membranes covering the whole composition range were prepared and characterized with respect to chemical and physiochemical properties such as water uptake, phosphoric acid doping, oxidative stability, mechanical strength and proton conductivity...

  5. EPR and optical absorption studies of Cu{sup 2+} doped L-histidinium dihydrogen phosphate–phosphoric acid single crystal

    Energy Technology Data Exchange (ETDEWEB)

    Prabakaran, R.; Sheela, K. Juliet; Rosy, S. Margret [Department of Physics, Gandhigram Rural Institute—Deemed University, Gandhigram, Dindigul-624302, Tamilnadu (India); Radha Krishnan, S.; Shanmugam, V.M. [CSIR-Central Electrochemical Research Institute, Karaikudi-630006, Tamilnadu (India); Subramanian, P., E-mail: psmanian_gri@yahoo.com [Department of Physics, Gandhigram Rural Institute—Deemed University, Gandhigram, Dindigul-624302, Tamilnadu (India)

    2014-02-01

    The EPR spectra of Cu{sup 2+} in L-histidinium dihydrogen phosphate phosphoric acid at room temperature reveal the presence of two magnetically inequivalent Cu{sup 2+} sites in the lattice. The principal values of the g- and A-tensors indicate existence of rhombic symmetry around the Cu{sup 2+} ion. From the direction cosines of the principal values of the g- and A-tensors, the locations of Cu{sup 2+} in the lattice have been identified as substitutional sites. Optical absorption study shows four bands confirm the rhombic symmetry. Photoluminescence study also confirms the rhombic symmetry around the ions.

  6. Measurement and modeling of density and viscosity of n-octanol-kerosene-phosphoric acid solutions in a temperature range 293.15-333.15 K

    Science.gov (United States)

    Ye, Changwen; Pei, Xiangjun; Liu, J. C.

    2016-12-01

    Densities and viscosities have been measured for the n-octanol + aviation kerosene (AK) + phosphoric acid (H3PO4) system with the mass fraction of H3PO4 in the range from w = 0 to 0.26 and in the temperature of 293.15-333.15 K. According to the experimental data, the measured viscosities were found well correlated with the temperature and mass fraction of H3PO4, which were fitted to regression equations. The result shows that the dilution effect of AK is obvious under the same temperature and mass fraction of H3PO4.

  7. Recovery of uranium contained in phosphoric acid by a wet method and its transformation in a high-purity uraniferous concentrates

    International Nuclear Information System (INIS)

    Davister, A.; Dubreucq, A.; Granville, G.; Gray, H.

    1984-01-01

    There are altogether three plants in active operation today for the recovery of uranium contained in the phosphoric acid, two in the USA and one in Prayon in Belgium. All three utilize the same solvant, i.e. the Depa-Topo mixture. The Prayon plant was started up in May 1980. Phosphoric acid is desaturated before the extraction for a long time at a low temperature, totally free from mineral and organic solids and rid of its soluble humic matter until a clear acid of very low optical density is obtained. During the re-extraction of the first cycle, the reduction of U 6+ into U 4+ is effected by metallic iron, according to an original patented process which permits the reduction of the introduced iron to a strict minimum. At the end of the second cycle, an original technique permits the precipitation of a uranium and ammonium hydroxide, starting from the aqueous phase, first separated from the organic phase and purified as regards iron; because of this, the concentrate requires no roasting [fr

  8. Determination of Water Vapor Pressure Over Corrosive Chemicals Versus Temperature Using Raman Spectroscopy as Exemplified with 85.5% Phosphoric Acid

    DEFF Research Database (Denmark)

    Rodier, Marion; Li, Qingfeng; Berg, Rolf W.

    2016-01-01

    A method to determine the water vapor pressure over a corrosive substance was developed and tested with 85.5 ± 0.4% phosphoric acid. The water vapor pressure was obtained at a range of temperatures from ∼25 ℃ to ∼200 ℃ using Raman spectrometry. The acid was placed in an ampoule and sealed...... with a reference gas (either hydrogen or methane) at a known pressure (typically ∼0.5 bar). By comparing the Raman signals from the water vapor and the references, the water pressure was determined as a function of temperature. A considerable amount of data on the vapor pressure of phosphoric acid are available...... in the literature, to which our results could successfully be compared. A record value of the vapor pressure, 3.40 bar, was determined at 210 ℃. The method required a determination of the precise Raman scattering ratios between the substance, water, and the used reference gas, hydrogen or methane. In our case...

  9. Recovery of uranium from wet process by the chloridic leaching of phosphate rocks

    International Nuclear Information System (INIS)

    Santana, A.O.; Paula, H.C.B.; Dantas, C.C.

    1984-01-01

    Uranium was recovered from chloridic leach liquor of phosphate rocks by solvent extraction on a laboratory scale. The extractor system is a mixture of di-(2-ethylhexyl) phosphoric acid (D 2 EHPA) and tributyl-phosphate (TBP) in a varsol diluent. The uranium concentration is 150 ppm in the rocks and 12 ppm in the leach liquor. The phosphate rocks are leached on a semi-industrial scale for dicalcium phosphate production. The recovery process comprises the following steps: extraction, reextraction, iron removal and uranium precipitation. (orig./EF)

  10. Radiological assessment occupational radionuclides in a phosphoric acid plant; Evaluacion radiologica ocupacional y distribucion de radionucleidos en una planta de acido fosforico

    Energy Technology Data Exchange (ETDEWEB)

    Bolivar, J. P.; Garcia-Tenorio, R.

    2008-07-01

    On the frame of a research project devoted to the control of the exposure due to natural radiation in several NORM industries located at the South of Spain, a detailed to the production of phosphoric acid has been performed. In addition, the behaviour along the mentioned process of the different radionuclides involved has been analysed. It has been concluded that the effective dose which can be received by the workers of the plant is clearly below 1 mSv/year. And it has been demonstrated that the main route of occupational exposure corresponds to the external radiation due mainly to the permanent presence of a radioactive contamination source in different zones of the plant. This contamination source is associated to the presence of scales in the inner surfaces of pipes and equipment as well as to the presence of sludges in the phosphoric acid storage tanks, which in both cases contain elevated concentrations of 226{sup R}a. Moreover, the 222{sup R}n concentrations inside the plant do not overpass 100 Bq/m{sup 3}, which not constitutes a radiological problem. (Author) 9 refs.

  11. The sealing of second mandibular temporary molar pits and fissure with the laser of Nd: YAG, phosphoric acid and the glass ionomer cement

    International Nuclear Information System (INIS)

    Toda, Maria Aparecida

    2003-01-01

    The main of our study was to check the sealing of second mandibular temporary molar pits and fissure, in vitro, with the laser of Nd: YAG, phosphoric acid at 37% and the glass ionomer cement (CIV, Fuji IX GC).The proposal was to check the structural morphologic changes in the laser irradiation upon the enamel surface to watch the pits and fissure sealing with the glass ionomer cement use after the laser irradiation and to verify the efficiency of the 'double conditioning' (phosphoric acid + Nd: YAG). At the same time we watch the evolution of the temperature in the pulp chamber's inside. Our desire was to achieve a therapeutic alternative technic to prevent the dental caries. The Nd: YAG laser parameters were the same: 79 mJ of energy per pulse; frequency of 5 Hz; mean power of 0,4 W; optical fiber on contact of 320 μm diameter; fluency of 99,52 J/ cm 2 , assuming that the only differential was the time of the laser application on the enamel surface. The samples were prepared with this way: Laser Nd: YAG (53 second) + acid + CIV (Fuji IX); Laser Nd: YAG (53 s); Laser Nd: YAG (20 s + 20 s) + acid + CIV; Laser Nd: YAG (20 s + 20 s); Acid + CIV; Control. Through the scanning electron microscopy (MEV) we noticed fusion and resolidification regions due to the laser irradiation and a better adaptation of the glass ionomer cement when we did the 'double conditioning'. Concerning the temperature increase we can conclude that the echeloned period was the best recommended because the temperature was found in a pattern that would not cause any damage to the dental pulp. For future studies we suggest a longer relaxing time between the laser irradiation, a comparative study of this method with other lasers, the use of other sealing materials and the study with the permanent teeth. (author)

  12. Electrochemical reduction of oxygen on small platinum particles supported on carbon in concentrated phosphoric acid. 2. Effects of teflon content in the catalyst layer and baking temperature of the electrode

    Energy Technology Data Exchange (ETDEWEB)

    Maoka, T.

    1988-03-01

    A relation between hydrophobicity (or wettability) of a porous gas diffusion electrode for use in a phosphoric acid fuel cell and its cathode performance (activity toward electrochemical oxygen reduction) was examined. The hydrophobicity of the gas diffusion electrode was regulated by changing either the amount of Teflon (PTFE) content in the catalyst layer or baking temperature of the electrode. The Tafel slope or electrochemical oxygen reduction became twice as high as that of the ordinary electrode when the wettability of electrode toward phosphoric acid was high. This fact supports a flooded agglomerate model as the mode of this type of porous gas diffusion electrode.

  13. In Situ Formed Phosphoric Acid/Phosphosilicate Nanoclusters in the Exceptional Enhancement of Durability of Polybenzimidazole Membrane Fuel Cells at Elevated High Temperatures

    DEFF Research Database (Denmark)

    Zhang, Jin; Aili, David; Bradley, John

    2017-01-01

    -meso-silica. The results indicate that the optimum limit of PWA-meso-silica loading in the PA/PBI membranes is 15 wt%. Detaled analysis indicates that the mesoporous structure of the PWA-meso-silica framework disintegrates, forming phosphosilicate phases within the PBI polymeric matrix during fuel cell operation at 200°C......Most recently, we developed a phosphotungstic acid impregnated mesoporous silica (PWA-meso-silica) and phosphoric acid doped polybenzimidazole (PA/PBI) composite membrane for use in high temperature fuel cells and achieved exceptional durability under a constant current load of 200 mA cm−2 at 200°C...... for over 2700 h. In this work, the fundamental role of PWA-meso-silica in enhancing the stability of the PA/PBI membrane has been investigated. The microstructure, the PA uptake, swelling ratio, mechanical property and conductivity of PA/PBI/PWA-meso-silica composite membranes depend on the loading of PWA...

  14. Recovery of uranium from analytical waste solution

    International Nuclear Information System (INIS)

    Kumar, Pradeep; Anitha, M.; Singh, D.K.

    2016-01-01

    Dispersion fuels are considered as advance fuel for the nuclear reactor. Liquid waste containing significant quantity of uranium gets generated during chemical characterization of dispersion fuel. The present paper highlights the effort in devising a counter current solvent extraction process based on the synergistic mixture of D2EHPA and Cyanex 923 to recover uranium from such waste solutions. A typical analytical waste solution was found to have the following composition: U 3 O 8 (∼3 g/L), Al: 0.3 g/L, V: 15 ppm, Phosphoric acid: 3M, sulphuric acid : 1M and nitric acid : 1M. The aqueous solution is composed of mixture of either 3M phosphoric acid and 1M sulphuric acid or 1M sulphuric acid and 1M nitric acid, keeping metallic concentrations in the above mentioned range. Different organic solvents were tested. Based on the higher extraction of uranium with synergistic mixture of 0.5M D2EHPA + 0.125M Cyanex 923, it was selected for further investigation in the present work

  15. Determination of the activity concentration of {sup 230}Th in phosphoric acids produced in Brazil; Determinação da concentração de atividade de {sup 230}Th em ácidos fosfóricos produzidos no Brasil

    Energy Technology Data Exchange (ETDEWEB)

    Taddei, M.H.T.; Ferreira, M.T.; Fukuma, H.T.; Xavier, T.T.; Sousa, F.V.T.S., E-mail: tatianattx@gmail.com [Comissao Nacional de Energia Nuclear (LAPOC/CNEN), Pocos de Caldas, MG (Brazil). Laboratorio de Pocos de Caldas. Radioquimica

    2017-07-01

    The high uranium phosphate rock from Itataia, Brazil, was processed using the wet route in the dihydrate system to manufacture phosphoric acid. The uranium contained in phosphoric acid was recovered by the solvent extraction technique. The distribution of the long half-life radionuclides from the decay series of {sup 238}U and {sup 232}Th were evaluated in these processes. The {sup 26}Ra, {sup 228}Ra and {sup 210}Pb radionuclides were found predominantly in phosphogypsum, while the isotopes of {sup 228}Th, {sup 230}Th and {sup 232}Th predominated in phosphoric acid after extracting uranium. The main concern in the commercialization of phosphoric acid that will be produced in the Itataia plant is in relation to the content of {sup 230}Th. This work determined the content of these radionuclides in phosphoric acid from different locations in the country in order to compare.

  16. Hydrogen Oxidation on Gas Diffusion Electrodes for Phosphoric Acid Fuel Cells in the Presence of Carbon Monoxide and Oxygen

    DEFF Research Database (Denmark)

    Gang, Xiao; Li, Qingfeng; Hjuler, Hans Aage

    1995-01-01

    Hydrogen oxidation has been studied on a carbon-supported platinum gas diffusion electrode in a phosphoric acidelectrolyte in the presence of carbon monoxide and oxygen in the feed gas. The poisoning effect of carbon monoxide presentin the feed gas was measured in the temperature range from 80...... to 150°C. It was found that throughout the temperaturerange, the potential loss due to the CO poisoning can be reduced to a great extent by the injection of small amounts ofgaseous oxygen into the hydrogen gas containing carbon monoxide. By adding 5 volume percent (v/o) oxygen, an almost...

  17. Investigation of the synergistic effect of alcoholic compounds on the extraction of H3PO4 from Syrian wet phosphoric acid by TBP

    International Nuclear Information System (INIS)

    Abdulbaki, M. K.; Shino, O.; Wahoud, A.

    2006-01-01

    This paper studies the synergistic effects of alcoholic compounds such as isoamyl alcohol. Pentanol, hexanol and heptanol on the extraction of H 3 PO 4 from Syrian phosphoric acid by (TBP). The possibility to use these alcoholic compounds as a diluent instead of kerosene was also studied. The results show that the alcoholic compounds has bigger extraction yield than (TBP) diluted in kerosene. The alcoholic compounds has an important synergistic effect, when it was used as a diluent instead of kerosene, on the extraction of H 3 PO 4 by (TBP) and they have a bigger extraction yield and the quicker phase separation comparing with kerosene. Extraction of uranium, fluoride, sulfate and heavy metals is relatively small. (Authors)

  18. Use of [18O4] phosphoric acid in the quantitation of phosphate by gas-liquid chromatography-mass spectrometry analysis

    International Nuclear Information System (INIS)

    Graff, G.; Krick, T.P.; Walseth, T.F.; Goldberg, N.D.

    1980-01-01

    A procedure is described to quantitate inorganic phosphate in the form of the tris(trimethylsilyl) (TMS) phosphate by gas-liquid chromatography-mass spectrometry (glc-ms) that increases the previously reported detection limit from the microgram to the nanogram range. The sensitivity for detecting TMS-phosphate by glc-ms analysis was shown to be limited by an increasing fractional loss with decreasing concentrations of TMS-phosphate analyzed due to its adsorption on different types of glc column supports. The method developed employs [ 18 O 4 ] phosphoric acid which serves as both an internal standard to permit quantitation and as a carrier to minimize sample adsorption on the glc column support

  19. Treatment of phosphorus-uraniferous solution

    International Nuclear Information System (INIS)

    Araujo Figueiredo, C. de.

    1984-01-01

    A solvent extraction process for the recovery of uranium from Itataia wet process phosphoric acid was studied. The proposed process consists of two extraction cycles. Uranium, reduced to its tetravalent state, is extracted in the first cycle using octylpyrosphoric acid (OPPA) in a kerosene type diluent. Stripping is accomplished with concentrated raffinate phosphoric acid and an oxidizing agent, in order to convert U (IV) to its hexavalent state. The strip solution from the first cycle is processed in the second cycle with the synergistic combination of di-( 2- ethylhexyl) phosphoric acid and tri-n-octylphosphine oxide (D2EHPA-TOPO). The extract is scrubbed and uranium is stripped with ammonium carbonate solution and recovered as a commercial concentrate. The results obtained from batch tests were used to set up a bench scale array of mixer settlers so as to demonstrate the process. (Author) [pt

  20. Practical applications of phosphors

    CERN Document Server

    Yen, William M; Yamamoto, Hajime

    2006-01-01

    Drawn from the second edition of the best-selling Phosphor Handbook, Practical Applications of Phosphors outlines methods for the production of various phosphors and discusses a broad spectrum of applications. Beginning with methods for synthesis and related technologies, the book sets the stage by classifying and then explaining practical phosphors according to usage. It describes the operating principle and structure of phosphor devices and the phosphor characteristics required for a given device, then covers the manufacturing processes and characteristics of phosphors. The book discusses research and development currently under way on phosphors with potential for practical usage and touches briefly on phosphors that have played a historical role, but are no longer of practical use. It provides a comprehensive treatment of applications including lamps and cathode-ray tubes, x-ray and ionizing radiation, and for vacuum fluorescent and field emission displays and covers inorganic and organic electroluminescen...

  1. Distribution equilibria of Eu(III) in the system: bis(2-ethylhexyl)phosphoric acid organic diluent-NaCl, lactic acid, polyaminocarboxylic acid, water

    International Nuclear Information System (INIS)

    Danesi, P.R.; Cianetti, C.; Horwitz, E.P.

    1982-01-01

    The distribution equilibria of Eu 3+ between aqueous phases containing lactic acid and N'-(2hydroxyethyl)ethylenediamine-N,N,N'-triacetic acid (HEDTA) or diethylenetriamine-N,N,N',N',N''-penetaacetic acid (DTPA) at constant ionic strength (μ = 1.0), and n-dodecane solutions of HDEHP have been studied. The formation constants of the simple Eu-lactate complexes and Eu-lactate-HEDTA mixed complex were evaluated from the k/sub d/ data. The conclusion is reached that no lactic acid is coextracted into the organic phase at tracer metal concentrations. The separation factors between Eu 3+ , Pm 3+ , and Am 3+ have been evaluated in the presence of HEDTA

  2. Using fractional extraction method to separate Mo from U in high concentration solution

    International Nuclear Information System (INIS)

    Zhao Pinzhi; Cheng Guangrong; Ma Xiuhua

    1996-01-01

    The author presents investigation on separating Mo from U in acid high concentration lixivium with fractional extraction of secondary amine (7203) and D2EHPA and preparing qualified products of ammonium molybdate and sodium diuranate

  3. Rare earth phosphors and phosphor screens

    International Nuclear Information System (INIS)

    Buchanan, R.A.; Maple, T.G.; Sklensky, A.F.

    1981-01-01

    Advances in the use of stabilized rare earth phosphors and of conversion screens using these materials are examined. In particular the new phosphors discussed in this invention consist of oxybromides of yttrium, lanthanum and gadolinium with a luminescent activator ion stabilized by an oxychloride or oxyfluoride surface layer and the conversion screens include trivalent cerium as the activator ion. (U.K.)

  4. Evaluation of human dental loss caused by carbamide peroxide bleacher compared with phosphoric acid conditioning - radioactive method; Avaliacao da perda dental humana com o uso do clareador peroxido de carbamida comparado ao condicionamento com acido fosforico - metodo radiometrico

    Energy Technology Data Exchange (ETDEWEB)

    Adachi, Eduardo Makoto; Yousseff, Michel Nicolau [Sao Paulo Univ., SP (Brazil). Faculdade de Odontologia. Dept. de Dentistica; Saiki, Mitiko [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil). Lab. de Analise por Ativacao Neutronica

    2002-07-01

    The radiometric method was applied to the evaluation of dental loss caused by carbamide peroxide when it is applied on the surface layers of enamel and dentin tissues. Also the dental loss caused by the etching with 37% phosphoric acid procedure used in aesthetic restoration was assessed for comparison with those results obtained. The tooth samples irradiated with a P standard in a thermal neutron flux of the nuclear reactor were placed in contact with 10% carbamide peroxide or with 37% phosphoric acid solution. The radioactivity of {sup 32} P transferred from the radioactive teeth to the bleaching gel or to etching acid was measured using a Geiger Muller detector to calculate the mass of P removed in this treatment and losses were calculated after obtaining their P concentrations. Results obtained indicated that enamel and dentin exposed to carbamide peroxide bleaching agent lose phosphorus. The extent of enamel loss was smaller than that obtained for dentin. In the case of acid etching, there was no difference between the results obtained for enamel and dentin loss. Also the dentin loss obtained after a treatment of 30 applications of 10% carbamide peroxide was the same magnitude of that one application of 37% phosphoric acid. (author)

  5. Fundamentals of phosphors

    CERN Document Server

    Yen, William M; Yamamoto, Hajime

    2006-01-01

    Drawing from the second edition of the best-selling Handbook of Phosphors, Fundamentals of Phosphors covers the principles and mechanisms of luminescence in detail and surveys the primary phosphor materials as well as their optical properties. The book addresses cutting-edge developments in phosphor science and technology including oxynitride phosphors and the impact of lanthanide level location on phosphor performance.Beginning with an explanation of the physics underlying luminescence mechanisms in solids, the book goes on to interpret various luminescence phenomena in inorganic and organic materials. This includes the interpretation of the luminescence of recently developed low-dimensional systems, such as quantum wells and dots. The book also discusses the excitation mechanisms by cathode-ray and ionizing radiation and by electric fields to produce electroluminescence. The book classifies phosphor materials according to the type of luminescence centers employed or the class of host materials used and inte...

  6. Studies on Three Liquid Phase Extraction (TLPE) system for separation of rare earths

    International Nuclear Information System (INIS)

    Yadav, Kartikey K.; Singh, D.K.; Anitha, M.; Singh, H.

    2014-01-01

    Three-liquid-phase extraction (TLPE) is relatively a new separation technique, which takes the advantage of the differences in physicochemical properties of three coexisted phases to achieve multi-phase liquid separation of two or more components in one-step extraction. TLPE system consists of three liquid layers namely an organic solvent phase (organophosphorous type) and two aqueous phases one rich in polymer phase (poly alkylene glycol) and other a salt solution. To study the feasibility of using such system for separation of rare earths, it is important to optimize the preparatory conditions by selective suitable polymer and salt solutions at an appropriate pH to obtain a stable three phase layers to effect the separation. D2EHPA (di-2-ethyl hexyl phosphoric acid) is a well- established extractant in the rare earth industry and has been chosen in the present work to form a TLPE with polymer and salt solution. In the present investigation after preparing the stable three phase, the feasibility of using TLPE has been examined to separate rare earths from a multicomponent solutions. This study has demonstrated the ability of TLPE having D2EHPA as organic phase to separate rare earths from a multicomponent system. Effect of pH, concentration and types of polymer, complexing agent and D2EHPA concentration has been studied. Variation in pH study indicated that 4.0 leads to extraction of rare earths in the polymer phase. PEG 600 was found to be best amongst the polymer investigated. Presence of DTPA as complexing agent in the salt solution having pH >4.0 resulted in enhanced extraction of rare earths in PEG phase

  7. Extraction equilibria of amino acids by Di (2-ethylhexyl) phosphoric acid in n-heptane solutions; Di (2-ethylhexyl) rinsan no n-heptane yoeki ni yoru aminosan no chushutsu heiko

    Energy Technology Data Exchange (ETDEWEB)

    Takahashi, M. [Suzuka National College of Technology, Mie (Japan); Tani, F. [Toyohashi University of Technology, Aichi (Japan); Kawai, Y. [Wako Jyunyaku Co. Ltd., Osaka (Japan); Takeuchi, H. [Nagoya University, Nagoya (Japan). Faculty of Engineering

    1997-03-10

    The extraction equilibria (i.e., distribution ratio) of amino acids by Di (2-ethyl hexyl) phosphoric acid in n-heptane solutions was investigated at a temperature of 298.2 K in the low pH range (of 2 to 5). The equal amount of an amino acid solution and an extracted solution with the predetermined concentration were shaken using a flask, and the concentration of amino acid in water phase was analyzed by a ninhydrin method. The concentration in organic phase was obtained by the concentration analysis in water phase and the material balance method after the amino acid is back-extracted by solution hydrochloride. The distribution ratio is in inverse proportion to the hydrogen ion concentration and in proportion to the 0.5th power of extracted agent concentration. The equilibrium constant is 0.650, 0.420, 0.320, 0.275, 0.064, and 0.040 mol{sup 0.5}/m{sup 1.5} in L-phenylalanine, L-tryptophane, L-leucine, L-methionine, glycine, and L-alanine, respectively. The equilibrium constant of the largest L-phenylalanine is 16 times as high as the smallest alanine. The extracted equilibrium constant increased as the hydrophobic property of amino acid increases. 18 refs., 10 figs., 1 tab.

  8. Characteristics of transfer of europium ions from phosphoric acid solution into the CaSO4·O.5H2O solid phase

    International Nuclear Information System (INIS)

    Berdonosova, D.G.; Burlakova, E.V.; Yasenkova, M.A.; Ivanov, L.N.; Melikhov, I.V.

    1989-01-01

    The mechanism of formation of the precipitated CaSO 4 ·0.5H 2 O phase was studied in detail; the precipitation was performed at 80 degree, equimolar solutions of Ca(H 2 PO 4 ) 2 and H 2 SO 4 in phosphoric acid of 38% concentration being used. The availability of detailed information on the mechanism of formation of CaSO 4 ·0.5H 2 O precipitates determined the choice of conditions of study of capture of rare earths. In particular, H 3 PO 4 of 38% P 2 O 5 concentration was used as the medium of formation of the calcium sulfate precipitate. Europium was chosen as the rare earth. Its behavior in the liquid and solid phases was studied by radiometric and luminescence methods. The radionuclide 152 Eu is convenient as a radioactive tracer while luminescence of europium is structure-sensitive; therefore, europium is often used in physicochemical investigations as a luminescent probe. It follows from the data that most of the europium captured by the precipitate during coagulation of the ultramicrocrystals is retained firmly by the solid phase. Therefore, in order to diminish capture of europium (and other rare earths) by the precipitate coagulation of the latter should be prevented

  9. Integrated Process for Ethanol, Biogas, and Edible Filamentous Fungi-Based Animal Feed Production from Dilute Phosphoric Acid-Pretreated Wheat Straw.

    Science.gov (United States)

    Nair, Ramkumar B; Kabir, Maryam M; Lennartsson, Patrik R; Taherzadeh, Mohammad J; Horváth, Ilona Sárvári

    2018-01-01

    Integration of wheat straw for a biorefinery-based energy generation process by producing ethanol and biogas together with the production of high-protein fungal biomass (suitable for feed application) was the main focus of the present study. An edible ascomycete fungal strain Neurospora intermedia was used for the ethanol fermentation and subsequent biomass production from dilute phosphoric acid (0.7 to 1.2% w/v) pretreated wheat straw. At optimum pretreatment conditions, an ethanol yield of 84 to 90% of the theoretical maximum, based on glucan content of substrate straw, was observed from fungal fermentation post the enzymatic hydrolysis process. The biogas production from the pretreated straw slurry showed an improved methane yield potential up to 162% increase, as compared to that of the untreated straw. Additional biogas production, using the syrup, a waste stream obtained post the ethanol fermentation, resulted in a combined total energy output of 15.8 MJ/kg wheat straw. Moreover, using thin stillage (a waste stream from the first-generation wheat-based ethanol process) as a co-substrate to the biogas process resulted in an additional increase by about 14 to 27% in the total energy output as compared to using only wheat straw-based substrates. ᅟ.

  10. Effect of the urease inhibitor phosphoric acid phenyl ester diamide on the utilization of urea-N in top dressing of spring wheat and oats

    Energy Technology Data Exchange (ETDEWEB)

    Matzel, W; Mueller, S; Lippold, H; Heber, R [Akademie der Landwirtschaftswissenschaften der DDR, Leipzig-Potsdam. Inst. fuer Duengungsforschung

    1979-01-01

    In pot experiments with spring wheat and oats the application of the urease inhibitor phosphoric acid phenyl ester diamide (PPDA) in addition to top dressing with /sup 15/N-urea revealed a 10% better utilization of the /sup 15/N-urea by the plant (related to the N amount applied). The loss-reducing effect of PPDA was especially felt when there were favourable conditions for NH/sub 3/ volatilization such as rapid hydrolysis of urea on the wet surface of light soil during shooting of the wheat. PPDA did not have any adverse influence on the course of the nitrogen uptake by the cereals during the time of shooting from the urea applied in top dressing. The utilization of the urea-N by the wheat, being about 5 to 6% lower in comparison to ammonium nitrate, under conditions that do not allow NH/sub 3/ losses, is to be attributed to the increased immobilization of the urea-N in the soil. The processes responsible for the nitrogen losses were concluded 3 to 4 weeks after top dressing to the cereals during the shooting period.

  11. Effect of the urease inhibitor phosphoric acid phenyl ester diamide on the utilization of urea-N in top dressing of spring wheat and oats

    International Nuclear Information System (INIS)

    Matzel, W.; Mueller, S.; Lippold, H.; Heber, R.

    1979-01-01

    In pot experiments with spring wheat and oats the application of the urease inhibitor phosphoric acid phenyl ester diamide (PPDA) in addition to top dressing with 15 N-urea revealed a 10% better utilization of the 15 N-urea by the plant (related to the N amount applied). The loss-reducing effect of PPDA was especially felt when there were favourable conditions for NH 3 volatilization such as rapid hydrolysis of urea on the wet surface of light soil during shooting of the wheat. PPDA did not have any adverse influence on the course of the nitrogen uptake by the cereals during the time of shooting from the urea applied in top dressing. The utilization of the urea-N by the wheat, being about 5 to 6% lower in comparison to ammonium nitrate, under conditions that do not allow NH 3 losses, is to be attributed to the increased immobilization of the urea-N in the soil. The processes responsible for the nitrogen losses were concluded 3 to 4 weeks after top dressing to the cereals during the shooting period. (author)

  12. Features of the Thermodynamics of Trivalent Lanthanide/Actinide Distribution Reactions by Tri-n-Octylphosphine Oxide and Bis(2-EthylHexyl) Phosphoric Acid

    Energy Technology Data Exchange (ETDEWEB)

    Travis S. Grimes; Peter R. Zalupski

    2014-11-01

    A new methodology has been developed to study the thermochemical features of the biphasic transfer reactions of trisnitrato complexes of lanthanides and americium by a mono-functional solvating ligand (tri-n-octyl phosphine oxide - TOPO). Stability constants for successive nitrato complexes (M(NO3)x3-x (aq) where M is Eu3+, Am3+ or Cm3+) were determined to assist in the calculation of the extraction constant, Kex, for the metal ions under study. Enthalpies of extraction (?Hextr) for the lanthanide series (excluding Pm3+) and Am3+ by TOPO have been measured using isothermal titration calorimetry. The observed ?Hextr were found to be constant at ~29 kJ mol-1across the series from La3+-Er3+, with a slight decrease observed from Tm3+-Lu3+. These heats were found to be consistent with enthalpies determined using van ’t Hoff analysis of temperature dependent extraction studies. A complete set of thermodynamic parameters (?G, ?H, ?S) was calculated for Eu(NO3)3, Am(NO3)3 and Cm(NO3)3 extraction by TOPO and Am3+ and Cm3+ extraction by bis(2-ethylhexyl) phosphoric acid (HDEHP). A discussion comparing the energetics of these systems is offered. The measured biphasic extraction heats for the transplutonium elements, ?Hextr, presented in these studies are the first ever direct measurements offered using two-phase calorimetric techniques.

  13. Investigation of electrolyte leaching in the performance degradation of phosphoric acid-doped polybenzimidazole membrane-based high temperature fuel cells

    Science.gov (United States)

    Jeong, Yeon Hun; Oh, Kyeongmin; Ahn, Sungha; Kim, Na Young; Byeon, Ayeong; Park, Hee-Young; Lee, So Young; Park, Hyun S.; Yoo, Sung Jong; Jang, Jong Hyun; Kim, Hyoung-Juhn; Ju, Hyunchul; Kim, Jin Young

    2017-09-01

    Precise monitoring of electrolyte leaching in high-temperature polymer electrolyte membrane fuel cell (HT-PEMFC) devices during lifetime tests is helpful in making a diagnosis of their quality changes and analyzing their electrochemical performance degradation. Here, we investigate electrolyte leaching in the performance degradation of phosphoric acid (PA)-doped polybenzimidazole (PBI) membrane-based HT-PEMFCs. We first perform quantitative analyses to measure PA leakage during cell operation by spectrophotometric means, and a higher PA leakage rate is detected when the current density is elevated in the cell. Second, long-term degradation tests under various current densities of the cells and electrochemical impedance spectroscopy (EIS) analysis are performed to examine the influence of PA loss on the membrane and electrodes during cell performance degradation. The combined results indicate that PA leakage affect cell performance durability, mostly due to an increase in charge transfer resistance and a decrease in the electrochemical surface area (ECSA) of the electrodes. Additionally, a three-dimensional (3-D) HT-PEMFC model is applied to a real-scale experimental cell, and is successfully validated against the polarization curves measured during various long-term experiments. The simulation results highlight that the PA loss from the cathode catalyst layer (CL) is a significant contributor to overall performance degradation.

  14. Fiscal 1994 survey report. Survey of factors causing degradation of phosphoric acid fuel cells; 1994 nendo rinsangata nenryo denchi no cell rekka yoin chosa hokokusho

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-03-01

    This survey aims to effectively promote studies for evaluating phosphoric acid fuel cell degradation. Data of time-dependent changes in voltage are collected from 58 plants now in operation (for 17,500 hours at the maximum). Half of them exhibit a degradation rate of 0.25-1%/1000 hours while degradation is abruptly accelerated midway in the other half. Causes for voltage drop are not known clearly. Since but a little systematically collected test data are available concerning the mechanism of cell degradation, it is decided that tests be conducted using small test model cells sharing the same specifications. Primary test conditions (combination of temperature, current, and pressure with test reference levels), performance evaluating methods (conditions of data collection), and methods of investigation by dismantling (items and frequency of investigations) are determined, and guidelines are provided for element tests for complementing the said test items and for studying their relations with the degradation mechanism. Based on acceleration-related factors to be obtained by common specification test cells, corporations involved will develop their own accelerated test methods. Small cells are fabricated for testing parameters, and model cells are specified. (NEDO)

  15. Facilitated transport of Cr(III) through activated composite membrane containing di-(2-ethylhexyl)phosphoric acid (DEHPA) as carrier agent

    International Nuclear Information System (INIS)

    Arslan, Gulsin; Tor, Ali; Cengeloglu, Yunus; Ersoz, Mustafa

    2009-01-01

    The facilitated transport of chromium(III) through activated composite membrane (ACM) containing di-(2-ethylhexyl) phosphoric acid (DEHPA) was investigated. DEHPA was immobilised by interfacial polymerisation on polysulfone layer which was deposited on non-woven fabric by using spin coater. Then, ACM was characterised by using scanning electron microscopy (SEM), contact angle measurements and atomic force microscopy (AFM). Initially, batch experiments of liquid-liquid distribution of Cr(III) and the extractant (DEHPA) were carried out to determine the appropriate pH of the feed phase and the results showed that maximum extraction of Cr(III) was achieved at a pH of 4. It was also found that Cr(III) and DEHPA reacted in 1/1 molar ratio. The effects of Cr(III) (in feed phase), HCl (in stripping phase) and DEHPA (in ACM) concentrations were investigated. DEHPA concentration varies from 0.1 to 1.0 M and it was determined that the transport of Cr(III) increased with the carrier concentration up to 0.8 M. It was also observed that the transport of Cr(III) through the ACM tended to increase with Cr(III) and HCl concentrations. The stability of ACM was also confirmed with replicate experiments.

  16. Facilitated transport of Cr(III) through activated composite membrane containing di-(2-ethylhexyl)phosphoric acid (DEHPA) as carrier agent

    Energy Technology Data Exchange (ETDEWEB)

    Arslan, Gulsin [Department of Chemistry, Selcuk University, 42031, Campus, Konya (Turkey); Tor, Ali, E-mail: ator@selcuk.edu.tr [Department of Environmental Engineering, Selcuk University, 42031 Campus, Konya (Turkey); Cengeloglu, Yunus; Ersoz, Mustafa [Department of Chemistry, Selcuk University, 42031, Campus, Konya (Turkey)

    2009-06-15

    The facilitated transport of chromium(III) through activated composite membrane (ACM) containing di-(2-ethylhexyl) phosphoric acid (DEHPA) was investigated. DEHPA was immobilised by interfacial polymerisation on polysulfone layer which was deposited on non-woven fabric by using spin coater. Then, ACM was characterised by using scanning electron microscopy (SEM), contact angle measurements and atomic force microscopy (AFM). Initially, batch experiments of liquid-liquid distribution of Cr(III) and the extractant (DEHPA) were carried out to determine the appropriate pH of the feed phase and the results showed that maximum extraction of Cr(III) was achieved at a pH of 4. It was also found that Cr(III) and DEHPA reacted in 1/1 molar ratio. The effects of Cr(III) (in feed phase), HCl (in stripping phase) and DEHPA (in ACM) concentrations were investigated. DEHPA concentration varies from 0.1 to 1.0 M and it was determined that the transport of Cr(III) increased with the carrier concentration up to 0.8 M. It was also observed that the transport of Cr(III) through the ACM tended to increase with Cr(III) and HCl concentrations. The stability of ACM was also confirmed with replicate experiments.

  17. Liquid–liquid equilibria study of the (water + phosphoric acid + hexyl or cyclohexyl acetate) systems at T = (298.15, 308.15, and 318.15) K: Measurement and thermodynamic modelling

    International Nuclear Information System (INIS)

    Ghanadzadeh Gilani, A.; Ghanadzadeh Gilani, H.; Shekarsaraee, S.; Nasiri-Touli, E.; Seyed Saadat, S.L.

    2016-01-01

    Highlights: • Tie line data for aqueous solutions of phosphoric acid with esters were obtained. • The LLE data were correlated using the UNIQUAC and NRTL models. • The quality of the LLE data was validated using the appropriate equations. • Separation factors were calculated for the chosen solvents. - Abstract: Liquid–liquid equilibrium (LLE) data for the (water + phosphoric acid + n-hexyl acetate or cyclohexyl acetate) ternary systems were determined at T = (298.15, 308.15 and 318.15) K and p = 101.3 kPa. The cloud point method was used to obtain the solubility and the Karl-Fischer, acidimetric titration, and refractive index methods were used to determine the tie-line values. Both the ternary systems exhibit type-1 behavior of LLE. The experimental values were regressed and acceptably correlated using the UNIQUAC and NRTL models. The reliability of the experimental tie lines was confirmed using the Othmer–Tobias plot. Experimental distribution coefficients and separation factors were fitted using the Kamlet–Taft LSER model. The influence of temperature on the biphasic area and separation factor was found to be minor. As a result, both the esters are suitable separating agents for aqueous phosphoric acid mixtures.

  18. Hydrometallurgical recovery of metal values from sulfuric acid leaching liquor of spent lithium-ion batteries.

    Science.gov (United States)

    Chen, Xiangping; Chen, Yongbin; Zhou, Tao; Liu, Depei; Hu, Hang; Fan, Shaoyun

    2015-04-01

    Environmentally hazardous substances contained in spent Li-ion batteries, such as heavy metals and nocuous organics, will pose a threat to the environment and human health. On the other hand, the sustainable recycling of spent lithium-ion batteries may bring about environmental and economic benefits. In this study, a hydrometallurgical process was adopted for the comprehensive recovery of nickel, manganese, cobalt and lithium from sulfuric acid leaching liquor from waste cathode materials of spent lithium-ion batteries. First, nickel ions were selectively precipitated and recovered using dimethylglyoxime reagent. Recycled dimethylglyoxime could be re-used as precipitant for nickel and revealed similar precipitation performance compared with fresh dimethylglyoxime. Then the separation of manganese and cobalt was conducted by solvent extraction method using cobalt loaded D2EHPA. And McCabe-Thiele isotherm was employed for the prediction of the degree of separation and the number of extraction stages needed at specific experimental conditions. Finally, cobalt and lithium were sequentially precipitated and recovered as CoC2O4 ⋅ 2H2O and Li2CO3 using ammonium oxalate solution and saturated sodium carbonate solution, respectively. Recovery efficiencies could be attained as follows: 98.7% for Ni; 97.1% for Mn, 98.2% for Co and 81.0% for Li under optimized experimental conditions. This hydrometallurgical process may promise a candidate for the effective separation and recovery of metal values from the sulfuric acid leaching liquor. Copyright © 2015 Elsevier Ltd. All rights reserved.

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

    International Nuclear Information System (INIS)

    Johny, W.S.; Raldi-Artono-Koestoer; Kris-Tri-Basuki; Sudibyo

    1996-01-01

    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 D 2 EHPA 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 HNO 3 was Kd y = 2.945 and Kd D y = 0.019

  20. Phosphor scintillator structure

    International Nuclear Information System (INIS)

    Cusano, D.A.; Prener, J.S.

    1980-01-01

    A method of fabricating scintillators is described in which the phosphor is distributed within the structure in such a way as to enhance the escape of the visible wavelength radiation that would otherwise be dissipated within the scintillator body. Two embodiments of the present invention are disclosed: one in which the phosphor is distributed in a layered structure and another in which the phosphor is dispersed throughout a transparent matrix. (U.K.)

  1. Synergistic extraction of europium(III) in ammonium ionic liquid

    International Nuclear Information System (INIS)

    Rout, Alok; Venkatesan, K.A.; Antony, M.P.

    2016-01-01

    Room temperature ionic liquids have been receiving increased attention for possible applications in the area of nuclear fuel reprocessing and waste management due to their fascinating properties such as good ionicity, high solvation capability, properties tunable etc. Most of the studies in the literature on the extraction of metal ions with molecular extractants dissolved in ionic liquid diluents are making use of the hydrophobic ionic liquids containing imidazolium cations such as the 1-alkyl-3-methylimidazolium ion. From an environmental point of view, such ionic liquids are not suitable as the primary mode of the metal extraction is by cation exchange mechanism wherein ionic liquid cation is lost to the aqueous phase leading to aqueous contamination and issue of recyclability of organic phase. However, there are some hydrophobic ionic liquids such as trioctylmethylammonium chloride ((N 1888 )(Cl)), and trihexyl(tetradecyl)phoshonium chloride (Cyphos IL 101) that exhibit no cation exchange in the aqueous phase during extraction. In this context, the extraction behavior of europium(III) using a neutral extractant, octyl, phenyl-N.N-diisobutylmethylcarbamoylphophinoxide (CMPO) and/or an acidic extractant bis(ethylhexyl)phosphoric acid (D2EHPA) dissolved in the ammonium ionic liquid diluent, trioctylmethylammonium bis(trifluoromethanesulfonyl)imide, (N 1888 )(NTf 2 ). The extraction behavior of CMPO (or D2EHPA)/(N 1888 )((Tf 2 ) system was investigated as a function of different extraction parameters such as feed acidity, extractant concentration, equilibration time etc.

  2. A contribution to the study of thorium and neptunium (IV) complexes in acidic phosphoric media; Contribution a l`etude des complexes de thorium et de neptunium (IV) en milieux phosphoriques acides

    Energy Technology Data Exchange (ETDEWEB)

    Ghafar, M

    1995-11-30

    The thorium and neptunium (IV) phosphate complexes formation in acidic media has been investigated, essentially at the indicator`s level with {sup 227} Th, {sup 234} Th, {sup 235} Np and {sup 239} Np. Solvent extraction, a commonly used method for determining stability constants in solutions, was used with HDEHP in toluene. In order to get a better understanding of inorganic transparent gels formation in phosphoric aqueous solutions, the effect of the thorium concentration is also studied. Specific experimental conditions have been chosen in order to avoid the formation of chelate and hydrolysis in the aqueous solution. The equilibrium constants and stability constants are calculated, and the results are compared with literature. The results show that increasing the thorium concentration does not lead to polymer forms. refs., 42 figs., 19 tabs.

  3. Transport of Eu3+ through a Bis(2-ethylhexyl)-phosphoric acid, n-dodecane solid supported liquid membrane

    International Nuclear Information System (INIS)

    Danesi, P.R.; Horwitz, E.P.; Rickert, P.

    1982-01-01

    The coupled transpot of Eu 3 + and H + ions througn a solid supported liquid membrane consisting of a porous polypropylene film immobilizing an HDEHP solution in n-dodecane has been studied as a function of the membrane area, stirring speed of the aqueous solutions, membrane composition, and acidity of the feed solution. The experimental results are in agreement with predictions derived from a theoretical permeability coefficient equation which assumes that membrane diffusion and aqueous film diffusion are the only rate-controlling factors

  4. Rirang uranium ore processing: continuous solvent extraction of uranium from Rirang ore acid digestion solution

    International Nuclear Information System (INIS)

    Riza, F.; Nuri, H. L.; Waluya, S.; Subijanto, A.; Sarono, B.

    1998-01-01

    Separation of uranium from Rirang ore acid digestion solution by means of continuous solvent extraction using mixer-settlers has been studied and a mixture of 0.3 M D2EHPA and 0.075 M TOPO extracting agent and kerosene diluent is employed to recover and separate uranium from Th, RE, phosphate containing solution. The experiments have been conducted batch-wise and several parameters have been studied including the aqueous to organic phase ratio, A/O, the extraction and the stripping times, and the operation temperature. The optimum conditions for extraction have been found to be A/O = 2 ratio, five minute extraction time per stage at room temperature. The uranium recovery of 99.07% has been achieved at those conditions whilst U can be stripped from the organic phase by 85% H 3 PO 4 solution with an O/A = 1 for 5 minutes stripping time per stage, and in a there stage operation at room temperature yielding a 100% uranium recovery from the stripping process

  5. Characterization and application of expanded graphite modified with phosphoric acid and glucose for the removal of Ni(II) from aqueous solution

    Science.gov (United States)

    Jiang, Li; Zhang, Jian; Xu, Xiaoli; Zhang, Jie; Liu, Hai; Guo, Zizhang; Kang, Yan; Li, Yiran; Xu, Jingtao

    2015-12-01

    Three kinds of modified expanded graphite (EG), impregnated with phosphoric acid (H3PO4) (P-EG), impregnated with glucose (G-EG), and impregnated with H3PO4 and glucose (G-P-EG), were prepared under a low temperature (150 °C). The adsorption capacity of G-P-EG (Qm = 7.016 mg/g) is much higher than original expanded graphite (EG Qm = 0.423 mg/g) and other two kinds of modified expanded graphite (P-EG Qm = 0.770 mg/g; G-EG Qm = 0.507 mg/g). The physicochemical properties of EG and G-P-EG were characterized by N2 adsorption/desorption, Boehm's titration and X-ray photoelectron spectroscopy (XPS). EG exhibited higher values of BET surface area (11.357 m2/g) and total pore volume (0.0303 cm3/g) than that of G-P-EG (4.808 m3/g and 0.0109 cm3/g). However, the results of Bohm's titration and XPS showed that G-P-EG contained more surface oxygen-containing functional groups. The Ni(II) adsorption equilibrium data agreed well with the Langmuir model. And the experimental data of EG and G-P-EG fitted better by pseudo-second order model. Based on the results of batch adsorption experiments and XPS analysis, there were several possible mechanisms for Ni(II) adsorption on the G-P-EG, including chemical adsorption, cation exchange, electrostatic attraction and surface complication.

  6. Features of the thermodynamics of trivalent lanthanide/actinide distribution reactions by tri-n-octylphosphine oxide and bis(2-ethylhexyl) phosphoric acid.

    Science.gov (United States)

    Grimes, Travis S; Zalupski, Peter R; Martin, Leigh R

    2014-11-06

    A new methodology has been developed to study the thermochemical features of the biphasic transfer reactions of trisnitrato complexes of lanthanides and americium by a monofunctional solvating ligand (tri-n-octylphosphine oxide, TOPO). Stability constants for successive nitrato complexes (M(NO3)x(3-x)(aq) where M is Eu(3+), Am(3+), or Cm(3+)) were determined to assist in the calculation of the extraction constant, K(ex), for the metal ions under study. Enthalpies of extraction (ΔH(extr)) for the lanthanide series (excluding Pm(3+)) and Am(3+) by TOPO have been measured using isothermal titration calorimetry. The observed ΔH(extr) were found to be constant at ~29 kJ mol(-1) across the series from La(3+) to Er(3+), with a slight decrease observed from Tm(3+) to Lu(3+). These heats were found to be consistent with enthalpies determined using van't Hoff analysis of temperature dependent extraction studies. A complete set of thermodynamic parameters (ΔG, ΔH, ΔS) was calculated for Eu(NO3)3, Am(NO3)3, and Cm(NO3)3 extraction by TOPO and Am(3+) and Cm(3+) extraction by bis(2-ethylhexyl) phosphoric acid (HDEHP). A discussion comparing the energetics of these systems is offered. The measured biphasic extraction heats for the transplutonium elements, ΔH(extr), presented in these studies are the first ever direct measurements offered using two-phase calorimetric techniques.

  7. Comparative study of kinetic reaction of 4,4′-Methylenebis (2-m ethel cyclo hexyl amine) with dimeric fatty acid c36 by use of a catalyst of phosphoric acid and dioxide manganese

    International Nuclear Information System (INIS)

    Al-Mohanna, N.; Al-Mohammad, H.

    2015-01-01

    Kinetic study was carried out on the reaction between 4,4′-Methylenebis (2-methylcyclohexylamine and dimeric fatty acid C 3 6 in molten state by use a catalyst of phosphoric acid and dioxide manganese the reaction was performed at 150 o C, and followed by determining the acid value of the product the polyamidation reaction was found to be of overall a second order until equilibrium state moreover the reaction was faster in the presence of the dioxide manganese polyamidation reaction was automatic where the value of free energy was negative the kinetics of thermal degradation was studied by use of thermogravimetric analysis (TGA) and was found to be of overall a second order and was followed by determining the thermodynamic constants of the thermal degradation reaction melting points and transitional glass in the presence of the catalyst were determined by use of differential calorimetry scanning (DSC) and was found to be close the degree of polymerization number average molecular weight and weight average molecular weight have been calculated during different times we noticed that the relationship between degree of polymerization and number average molecular weight, weight average molecular weight with time is linear until equilibrium state the prepared polyamide involve crystallization and amorphous area this was shown by XRD spectra. (author)

  8. Re-processing CRT phosphors for mercury-free applications

    International Nuclear Information System (INIS)

    Dexpert-Ghys, Jeannette; Regnier, Sophie; Canac, Sophie; Beaudette, Tristan; Guillot, Philippe; Caillier, Bruno; Mauricot, Robert; Navarro, Julien; Sekhri, Salem

    2009-01-01

    This study is part of an operation in the framework of treatment and revalorization of IEEE (Informatics, Electronics and related) wastes. It aims to recover the active phosphors in cathode ray tubes (CRTs) and to re-cycle these powders by appropriate treatments as phosphors for mercury-free applications such as plasma display panels, flat lamps, advertising and lighting. The studied waste comes from a large panel of CRTs from any supplier. Several thermo-chemical treatments have been investigated. The removal of zinc sulfide-based phosphors and the recovery of a red phosphor Y 2 O 3 :Eu 3+ has been achieved by one (basic attack) route. The photoluminescence efficiency under VUV excitation of the obtained powders is at most 30% that of a commercial phosphor. The second route (acid attack) appears less promising. It has been established that silicate-based impurities could prevent isolating the yttrium based phosphor.

  9. Re-processing CRT phosphors for mercury-free applications

    Energy Technology Data Exchange (ETDEWEB)

    Dexpert-Ghys, Jeannette, E-mail: jdexpert@cemes.f [CEMES, 29 rue Jeanne Marvig, BP 94347, 31055 Toulouse cedex 4 (France); Regnier, Sophie; Canac, Sophie [ICAM, 75 avenue de Grande Bretagne, 31300 Toulouse (France); Beaudette, Tristan; Guillot, Philippe; Caillier, Bruno [DPHE, Universite Jean Francois Champollion, place de Verdun, 81012 Albi cedex 9 (France); Mauricot, Robert; Navarro, Julien [CEMES, 29 rue Jeanne Marvig, BP 94347, 31055 Toulouse cedex 4 (France); Sekhri, Salem [ENVOI, Cheminement Glueck, 31100 Toulouse (France)

    2009-12-15

    This study is part of an operation in the framework of treatment and revalorization of IEEE (Informatics, Electronics and related) wastes. It aims to recover the active phosphors in cathode ray tubes (CRTs) and to re-cycle these powders by appropriate treatments as phosphors for mercury-free applications such as plasma display panels, flat lamps, advertising and lighting. The studied waste comes from a large panel of CRTs from any supplier. Several thermo-chemical treatments have been investigated. The removal of zinc sulfide-based phosphors and the recovery of a red phosphor Y{sub 2}O{sub 3}:Eu{sup 3+} has been achieved by one (basic attack) route. The photoluminescence efficiency under VUV excitation of the obtained powders is at most 30% that of a commercial phosphor. The second route (acid attack) appears less promising. It has been established that silicate-based impurities could prevent isolating the yttrium based phosphor.

  10. Modelling and Optimization of Corrosion Inhibition of Mild Steel in Phosphoric Acid by Red Pomegranate Peels Aqueous Extract

    Directory of Open Access Journals (Sweden)

    Khalid Hamid Rashid

    2011-11-01

    Full Text Available Taguchi experimental design (TED is applied to find the optimum effectiveness of aqueous Red Pomegranate Peel (RPP extract as a green inhibitor for the corrosion of mild steel in 2M H3PO4 solution. The Taguchi methodology has been used to study the effects of changing, temperature, RPP concentration and contact period, at three levels. Weight-loss measurements were designed by construction a L9 orthogonal arrangement of experiments. Results of the efficiencies of inhibition were embraced for the signal to noise proportion & investigation of variance (ANOVA. The results were further processed with a MINITAB-17 software package to find the optimal conditions for inhibitor usage. Second order polynomial model was used for experimental data fitting. Optimum conditions for achieving the maximum corrosion inhibition efficiency are obtained from optimizing the above model and are found as follow: 39.66 °C temperature of acidic media, 38.29 ml/L inhibitor concentration and 2.95 h contact period. Results demonstrated that rate of corrosion was increased with temperature increasing & decreasing inhibitor concentration. It was concluded that the Taguchi design was adequately useful in the optimization of operating parameters and that RPP sufficiently inhibited the corrosion of steel at the range of variables studied.

  11. Effect of three organic amendments and of the lime on the readiness and the phosphorous adsorption in an acid soil

    International Nuclear Information System (INIS)

    Gomez L, Carmen Rosa; Narvaez C, Carlos Eduardo

    1999-01-01

    To observe the effects of the organic materials and lime on the availability and sorption of phosphorus in a strongly acid soil (Inceptic Hapludox), poor in P, a greenhouse experiment and a laboratory studied were conducted. Plastic pots were filled with 400 g of soil to which was given a basic N.P.K.S. fertilization with applications of 90 kg P 2 O-5 hectare chicken manure, compost or cowpea (Vigna Unguiculata) were added to soil at the rates of 0.0; 0,8 and 2,4 g O.M. 100 g - 1 separate soil samples were amended with 1,5 ton CaCO 3 hectare. Soils were incubated for periods of 2, 14 and 54 days; after each period, pH, exchangeable AL and available P were determined. In soils incubated 54 days, the P sorption was evaluated trough isotherms and was interrelated the available P with the P sorption. Either, organic materials or lime increased the available P. Chicken manure let levels between 25 and 120 mg P kg - 1 the compost between 12 and 37, the cowpea between 6 and 15 and the lime between 3 and 8 mg P kg - 1. The availability of phosphorus increase with increasing rates of the organics materials but is reduced upon elapsing the incubated period. The treatments decreased drastically exchangeable al and this had relationship to the increase of the available P. The behavior in the P sorption was fitted to freundlich equation. The basic fertilization did not modify the p sorption while the organic amendments and the lime reduced it in different degree. The value of K, in the expression of the isotherms, shows an important reduction of the P sorption capacity in soil, caused by the chicken manure. An inverse relationship was observed between the p available and the value of K

  12. Characterization of silica polymorphs in kaolins by X-ray diffraction before and after phosphoric acid digestion and thermal treatment

    International Nuclear Information System (INIS)

    Kahraman, Sibel; Oenal, Mueserref; Sarikaya, Yueksel; Bozdogan, Ihsan

    2005-01-01

    To characterize silica polymorphs (silicas) in some kaolins, orthophosphoric acid digestion (240 deg. C, 15 min), and thermal treatment (1050 deg. C, 24 h) were applied to eight samples. The original, digested, and heated samples were examined by X-ray diffraction (XRD). Crystalline silica quartz (SiO 2 ) was identified from the standard XRD patterns of the original kaolins; all contained quartz. On the other hand, hydrated partially crystalline silicas (SiO 2 .nH 2 O), such as well-ordered opal-C and opal-CT, were not readily distinguished from high-temperature crystalline silica, α-cristobalite, using standard XRD patterns of the original kaolins because, sharp and intense characteristic XRD peaks (h k l = 1 0 1) centered near 0.4 nm for opal-C, opal-CT, and α-cristobalite coincided. In order to distinguish these silicas the XRD patterns of the digested and heated samples were evaluated. It was observed that the 1 0 1 peaks disappear and sharpen in the course of digestion and heating, respectively. Because, the crystallinity of α-cristobalite does not change by these treatments, it was concluded that the kaolins contain opal-C and opal-CT or their mixtures in amorphous opal-A (SiO 2 .nH 2 O), but not α-cristobalite, which is probably human carcinogen. Because, the crystallinity increases in order opal-CT and opal-C, the narrowing in width at half-maximum peak height (FWHM) 1 0 1 must be more for opal-CT than opal-C by heating. Therefore, to distinguish opal-CT and opal-C from each other, the FWHM values before and after the heating process, were examined. Based on the results, it was estimated that six kaolins contain opal-CT in opal-A matrix, one kaolin contains only opal-A in a trace amount, and one kaolin contains non-opals

  13. A Study of ext ration equilibrium in the system:phosphoric acid produced in Aqaba-uranium-0.5 M de pa-0.125M TOPO diluted in kerosene

    International Nuclear Information System (INIS)

    Al-Matar, K.A.; Rawajfeh, M.K.

    1995-01-01

    The extraction of uranium from purified wet process Jordanian phosphoric acid by synergistic solvent 0.5 M de pa and 0.125 M TOPO diluted in kerosene has been studied as a function of temperature and electro-motive force. The uranium distribution coefficient was found to be directly proportional to the electro-motive force up to a limiting point. The uranium distribution coefficient was found to decrease with temperature.Distribution coefficients for the Jordanian acid were found to be higher than those for similar acids from elsewhere.An Aqueous to Organic phase ratio (A/O) recommended for use with the Jordanian acid is 2.5. 11 refs., 6 figs., 2 tab.(Author)

  14. Unactivated yttrium tantalate phosphor

    International Nuclear Information System (INIS)

    Reddy, V.B.; Cheung, H.K.

    1992-01-01

    This patent describes an unactivated yttrium tantalate phosphor having M prime monoclinic structure and containing one or more additives of Rb and Al in an amount of between about 0.001 to 0.1 moles per mole of yttrium tantalate to improve brightness under X-radiation. This patent also describes an unactivated yttrium tantalate phosphor having M prime monoclinic structure and containing additives of Sr in an amount of between 0.001 to 0.1 moles per mole of yttrium tantalate and one or more of Rb and Al in an amount of between 0.001 to 0.1 moles per mole of yttrium tantalate the phosphor exhibiting a greater brightness under X-radiation than the phosphor absent Rb and Al

  15. Low lag luminescent phosphors

    International Nuclear Information System (INIS)

    1976-01-01

    The addition of potassium or rubidium salts to europium-activated fluorohalide phosphors produces X-ray screens with low lag, even at very low europium concentrations. The chemical preparation and afterglow test results are described

  16. Characterization and application of expanded graphite modified with phosphoric acid and glucose for the removal of Ni(II) from aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Jiang, Li [Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Zhang, Jian, E-mail: zhangjian00@sdu.edu.cn [Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Xu, Xiaoli [Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Zhang, Jie [Shandong Experimental High School, Jinan 250100 (China); Liu, Hai; Guo, Zizhang; Kang, Yan; Li, Yiran [Shandong Key Laboratory of Water Pollution Control and Resource Reuse, School of Environmental Science and Engineering, Shandong University, Jinan 250100 (China); Xu, Jingtao [School of Municipal and Environmental Engineering, Shandong Jianzhu University, Jinan 250100 (China)

    2015-12-01

    Highlights: • Glucose and H{sub 3}PO{sub 4}, single or together, were used to modify expanded graphite. • The modified condition was at a low temperature (150 °C). • The properties of EG and the highest adsorption ability modified EG were compared. • G-P-EG has the highest adsorption ability, which is much higher than that of EG. - Abstract: Three kinds of modified expanded graphite (EG), impregnated with phosphoric acid (H{sub 3}PO{sub 4}) (P-EG), impregnated with glucose (G-EG), and impregnated with H{sub 3}PO{sub 4} and glucose (G-P-EG), were prepared under a low temperature (150 °C). The adsorption capacity of G-P-EG (Q{sub m} = 7.016 mg/g) is much higher than original expanded graphite (EG Q{sub m} = 0.423 mg/g) and other two kinds of modified expanded graphite (P-EG Q{sub m} = 0.770 mg/g; G-EG Q{sub m} = 0.507 mg/g). The physicochemical properties of EG and G-P-EG were characterized by N{sub 2} adsorption/desorption, Boehm's titration and X-ray photoelectron spectroscopy (XPS). EG exhibited higher values of BET surface area (11.357 m{sup 2}/g) and total pore volume (0.0303 cm{sup 3}/g) than that of G-P-EG (4.808 m{sup 3}/g and 0.0109 cm{sup 3}/g). However, the results of Bohm's titration and XPS showed that G-P-EG contained more surface oxygen-containing functional groups. The Ni(II) adsorption equilibrium data agreed well with the Langmuir model. And the experimental data of EG and G-P-EG fitted better by pseudo-second order model. Based on the results of batch adsorption experiments and XPS analysis, there were several possible mechanisms for Ni(II) adsorption on the G-P-EG, including chemical adsorption, cation exchange, electrostatic attraction and surface complication.

  17. Properties of Pt/C catalyst modified by chemical vapor deposition of Cr as a cathode of phosphoric acid fuel cell

    International Nuclear Information System (INIS)

    Seo, Sang Joon; Joh, Han-Ik; Kim, Hyun Tae; Moon, Sang Heup

    2006-01-01

    Cr-modified Pt/C catalysts were prepared by the chemical vapour deposition (CVD) of Cr on Pt/C, and their performance as a cathode of phosphoric acid fuel cell (PAFC) was compared with the case of catalysts containing Cr added by impregnation (IMP). The catalyst prepared by CVD showed a higher activity for oxygen reduction reaction (ORR) than one prepared by IMP. There was an optimum amount of Cr that yielded the maximum mass activity of the catalyst because the gain in the intrinsic activity due to the promotional effect of Cr was counterbalanced by the loss of exposed Pt surface area as a result of the Cr introduction. Nevertheless, the activity increase at the optimum amount of Cr was greater for the CVD catalyst than for the IMP catalyst. Also, the optimum amount of Cr to yield the maximum activity was smaller for the former catalyst [Cr/Pt] CVD = 0.6, than for the latter, [Cr/Pt] IMP = 1.0. The enhancement of the Pt catalyst activity by Cr addition is attributed to two factors: changes in the surface Pt-Pt spacing and the electronic modification of the Pt surface. The formation of a Pt-Cr alloy, as confirmed by X-ray diffraction, decreased the lattice parameter of Pt, which was beneficial to the catalyst activity for ORR. X-ray photoelectron spectroscopy results showed that the binding energies of Pt electrons were shifted to higher energies due to Cr modification. Accordingly, the electron density of Pt was lowered and the Pt-O bond became weak on the Cr-modified catalysts, which was also beneficial to the catalyst activity for ORR. The promotion of oxygen reduction on Cr-modified catalysts was confirmed by measuring the cyclic voltammograms of the catalysts. All the above changes were made more effectively for catalysts prepared by CVD than for those prepared by IMP because the former method allowed Cr to interact more closely with the Pt surface than the latter, which was demonstrated by the characterization of catalysts in this study

  18. Characterization and application of expanded graphite modified with phosphoric acid and glucose for the removal of Ni(II) from aqueous solution

    International Nuclear Information System (INIS)

    Jiang, Li; Zhang, Jian; Xu, Xiaoli; Zhang, Jie; Liu, Hai; Guo, Zizhang; Kang, Yan; Li, Yiran; Xu, Jingtao

    2015-01-01

    Highlights: • Glucose and H 3 PO 4 , single or together, were used to modify expanded graphite. • The modified condition was at a low temperature (150 °C). • The properties of EG and the highest adsorption ability modified EG were compared. • G-P-EG has the highest adsorption ability, which is much higher than that of EG. - Abstract: Three kinds of modified expanded graphite (EG), impregnated with phosphoric acid (H 3 PO 4 ) (P-EG), impregnated with glucose (G-EG), and impregnated with H 3 PO 4 and glucose (G-P-EG), were prepared under a low temperature (150 °C). The adsorption capacity of G-P-EG (Q m = 7.016 mg/g) is much higher than original expanded graphite (EG Q m = 0.423 mg/g) and other two kinds of modified expanded graphite (P-EG Q m = 0.770 mg/g; G-EG Q m = 0.507 mg/g). The physicochemical properties of EG and G-P-EG were characterized by N 2 adsorption/desorption, Boehm's titration and X-ray photoelectron spectroscopy (XPS). EG exhibited higher values of BET surface area (11.357 m 2 /g) and total pore volume (0.0303 cm 3 /g) than that of G-P-EG (4.808 m 3 /g and 0.0109 cm 3 /g). However, the results of Bohm's titration and XPS showed that G-P-EG contained more surface oxygen-containing functional groups. The Ni(II) adsorption equilibrium data agreed well with the Langmuir model. And the experimental data of EG and G-P-EG fitted better by pseudo-second order model. Based on the results of batch adsorption experiments and XPS analysis, there were several possible mechanisms for Ni(II) adsorption on the G-P-EG, including chemical adsorption, cation exchange, electrostatic attraction and surface complication.

  19. Effect of a low-viscosity adhesive resin on the adhesion of metal brackets to enamel etched with hydrochloric or phosphoric acid combined with conventional adhesives.

    Science.gov (United States)

    Yetkiner, Enver; Ozcan, Mutlu; Wegehaupt, Florian Just; Wiegand, Annette; Eden, Ece; Attin, Thomas

    2013-12-01

    This study investigated the effect of a low-viscosity adhesive resin (Icon) applied after either hydrochloric (HCl) or phosphoric acid (H3PO4) on the adhesion of metal brackets to enamel. Failure types were analyzed. The crowns of bovine incisors (N = 20) were sectioned mesio-distally and inciso-gingivally, then randomly assigned to 4 groups according to the following protocols to receive mandibular incisor brackets: 1) H3PO4 (37%)+TransbondXT (3M UNITEK); 2) H3PO4 (37%)+Icon+TransbondXT; 3) HCl (15%)+Icon (DMG)+TransbondXT 4) HCl (15%)+Icon+Heliobond (Ivoclar Vivadent)+TransbondXT. Specimens were stored in distilled water at 37°C for 24 h and thermocycled (5000x, 5°C to 55°C). The shear bond strength (SBS) test was performed using a universal testing machine (1 mm/min). Failure types were classified according to the Adhesive Remnant Index (ARI). Contact angles of adhesive resins were measured (n = 5 per adhesive) on ceramic surfaces. No significant difference in SBS was observed, implying no difference between combinations of adhesive resins and etching agents (p = 0.712; ANOVA). The Weibull distribution presented significantly lower Weibull modulus (m) of group 3 (m = 2.97) compared to other groups (m = 5.2 to 6.6) (p group 1 (45.4 ± 7.9) > group 2 (44.2 ± 10.6) > group 3 (42.6 ± 15.5). While in groups 1, 3, and 4 exclusively an ARI score of 0 (no adhesive left on tooth) was observed, in group 2, only one specimen demonstrated score 1 (less than half of adhesive left on tooth). Contact angle measurements were as follows: Icon (25.86 ± 3.81 degrees), Heliobond (31.98 ± 3.17 degrees), TransbondXT (35 ± 2.21 degrees). Icon can be safely used with the conventional adhesives tested on surfaces etched with either HCl or H3PO4.

  20. Phosphors for LED lamps

    Science.gov (United States)

    Murphy, James Edward; Manepalli, Satya Kishore; Kumar, Prasanth Nammalwar

    2013-08-13

    A phosphor, a phosphor blend including the phosphor, a phosphor prepared by a process, and a lighting apparatus including the phosphor blend are disclosed. The phosphor has the formula (Ca.sub.1-p-qCe.sub.pK.sub.q).sub.xSc.sub.y(Si.sub.1-rGa.sub.r).sub.zO.su- b.12+.delta. or derived from a process followed using disclosed amounts of reactants. In the formula, (0

  1. High temperature thermometric phosphors

    Science.gov (United States)

    Allison, Stephen W.; Cates, Michael R.; Boatner, Lynn A.; Gillies, George T.

    1999-03-23

    A high temperature phosphor consists essentially of a material having the general formula LuPO.sub.4 :Dy.sub.(x),Eu.sub.y) wherein: 0.1 wt %.ltoreq.x.ltoreq.20 wt % and 0.1 wt %.ltoreq.y.ltoreq.20 wt %. The high temperature phosphor is in contact with an article whose temperature is to be determined. The article having the phosphor in contact with it is placed in the environment for which the temperature of the article is to be determined. The phosphor is excited by a laser causing the phosphor to fluoresce. The emission from the phosphor is optically focused into a beam-splitting mirror which separates the emission into two separate emissions, the emission caused by the dysprosium dopant and the emission caused by the europium dopent. The separated emissions are optically filtered and the intensities of the emission are detected and measured. The ratio of the intensity of each emission is determined and the temperature of the article is calculated from the ratio of the intensities of the separate emissions.

  2. Contribution to the study of the physico-chemical mechanisms of metallic cation extraction by alkylphosphoric acids. Extraction of zirconium (IV) by di-2-ethylhexyl phosphoric acid (DEHPA)

    International Nuclear Information System (INIS)

    Carbonnier, J.-L.

    1979-02-01

    Extraction of zirconium, especially at high concentration (0.1M), by dodecane diluted DEHPA (HA) from hydrochloric or nitric aqueous phases of 0.1 to 10 M acidity was studied. The composition, structure and polymerisation of the complexes extracted were determined by chemical analysis, viscosimetry, infrared spectrometry and light scattering. A Zr(OH) 2 A 2 .2HNO 3 , type structure is proposed for these complexes instead of the generally accepted form: Zr(OH) 2 (NO 3 ) 2 .2HA. Similarly in hydrochloric solution: Zr(OH) 2 A 2 .2HCl. Polymerisation in the organic phase results from the juxtaposition of two factors; firstly zirconium saturation (formation of bridges by DEHPA between zirconium atoms) and secondly the nature the equeous phase. In slightly acid hydrochloric solution (pH = 1.3) the aqueous plymers of zirconium are extracted in the organic phase as polynuclear complexes; in nitric solution no polynuclear complexes are observed but the nitric acid molecules extracted set up hydrogen bonds which explain the increased viscosity and gelification of the organic phases [fr

  3. Color stable manganese-doped phosphors

    Science.gov (United States)

    Lyons, Robert Joseph [Burnt Hills, NY; Setlur, Anant Achyut [Niskayuna, NY; Deshpande, Anirudha Rajendra [Twinsburg, OH; Grigorov, Ljudmil Slavchev [Sofia, BG

    2012-08-28

    A process for preparing color stable Mn.sup.+4 doped phosphors includes providing a phosphor of formula I; A.sub.x[MF.sub.y]:Mn.sup.+4 I and contacting the phosphor in particulate form with a saturated solution of a composition of formula II in aqueous hydrofluoric acid; A.sub.x[MF.sub.y]; II wherein A is Li, Na, K, Rb, Cs, NR.sub.4 or a combination thereof; M is Si, Ge, Sn, Ti, Zr, Al, Ga, In, Sc, Y, La, Nb, Ta, Bi, Gd, or a combination thereof; R is H, lower alkyl, or a combination thereof; x is the absolute value of the charge of the [MF.sub.y] ion; and y is 5, 6 or 7. In particular embodiments, M is Si, Ge, Sn, Ti, Zr, or a combination thereof. A lighting apparatus capable of emitting white light includes a semiconductor light source; and a phosphor composition radiationally coupled to the light source, and which includes a color stable Mn.sup.+4 doped phosphor.

  4. Pt.3. Carbon-13 fractionation in the decomposition of formic acid initiated by phosphoric anhydride. 13C fractionation in the decomposition of HCOOH initiated by P2O5

    International Nuclear Information System (INIS)

    Zielinski, M.; Zielinska, A.

    1998-01-01

    13 C isotope effects in the decarbonylation of formic acid of natural isotopic composition initiated by phosphorus pentoxide have been studied in a large temperature range (-5 o C) - (+90 o C). The 13 C fractionation in the carbon monooxide production at -5 o C increased from a low value of 1.2% characteristic of the first fractions of consecutively controlled portions of carbon monooxide to higher values of 13 C KIE observed in the decarbonylation of pure formic acid at corresponding temperatures. The temperature and time dependences of the measured 13 C fractionation are functions of the relative number of milimoles of formic acid and the dehydrating phosphoric anhydride, P 2 O 5 . The addition of metaphosphoric acid reagent to unreacted formic acid containing H 3 PO 4 significantly increased the 13 C fractionation in subsequent decarbonylations at 70.4 o C but to a slightly less degree than expected ( 13 C KIE = 1.0503 instead 1.0535). The addition of metaphosphoric acid reagent to formic acid saturated with NaCl results in the experimental 13 C fractionation of the value of 1.0534 very close to the theoretical one. An explanation of the low values of 13 C KIE in the initial stages of HCOOH/P 2 O 5 decarbonylations has been presented. (author)

  5. Indium recovery by solvent extraction

    International Nuclear Information System (INIS)

    Fortes, Marilia Camargos Botelho

    1999-04-01

    Indium has been recovered as a byproduct from residues generated from the sulfuric acid leaching circuits in mineral plants for zinc recovery. Once its recovery comes from the slags of other metals recovery, it is necessary to separate it from the other elements which usually are present in high concentrations. Many works have been approaching this separation and indicate the solvent extraction process as the main technique used. In Brazilian case, indium recovery depends on the knowledge of this technique and its development. This paper describes the solvent extraction knowledge for the indium recovery from aqueous solutions generated in mineral plants. The results for determination of the best experimental conditions to obtain a high indium concentration solution and minimum iron poisoning by solvent extraction with di (2-ethylhexyl)-phosphoric acid (D2EHPA) solubilized in isoparafin and exxsol has been presented. (author)

  6. Separation and electrodeposited of 210 Po

    International Nuclear Information System (INIS)

    Ordonez R, E.; Iturbe G, J.L.

    1991-12-01

    Presently work it was determined the selective separation of the 210 Po that is in an uraniferous mineral, by means of acid leaching of the mineral and the purification was carried out by means of partition chromatography whose stationary phase is 2-ethylhexyl phosphoric acid (D 2 EHPA), it has been possible to isolate the 210 Po of the rest of the radioactive elements that conform the family 4 N +2 , the optimal elutriation conditions of this element were settled down of manner of not dragging other radioelements. Another of the achievements presented in this communication has been the electrodeposition of this element has more than enough stainless steel discs with a superior yield to 95%. (Author)

  7. Teor de fósforo e pH no bulbo molhado, com diferentes freqüências de fertirrigação, utilizando ácido fosfórico Phosphorous content and pH in the wet bulb, with diferent frequencies of fertigation using phosphoric acid

    Directory of Open Access Journals (Sweden)

    Leticia C. Foratto

    2007-08-01

    Full Text Available A aplicação de fertilizantes fosfatados, tais como superfosfofato simples, superfosfofato triplo e monofosfato de amônio, via gotejamento, pode apresentar incrustações nas canalizações e obstruções de emissores. No presente trabalho, realizado na UNESP/Jaboticabal - SP, estudaram-se a distribuição do fósforo e a sua influência sobre o pH e a umidade em Latossolo Vermelho, fertirrigado durante um mês, com cinco aplicações semanais de ácido fosfórico. Utilizaram-se quatro repetições e oito tratamentos, constituídos da combinação de doses de P2O5 (0 e 50 kg ha-1 e freqüências de aplicação de 1; 3; 5 e 7 dias. Pelos resultados obtidos, observou-se que a freqüência de irrigação ou de fertirrigação não influenciou na distribuição final da umidade no bulbo molhado; aplicando-se o ácido fosfórico, o pH do solo até 30 cm do gotejador e até 40 cm em profundidade foi reduzido, atingindo valor de 3,6, e o teor de fósforo foi maior nessa mesma porção do bulbo, ultrapassando 1.500 mg dm-3. Isso permite indicar que o ácido fosfórico pode ser utilizado em irrigação localizada, com controle do pH do solo, pois sua redução influencia no desenvolvimento das culturas e, conseqüentemente, na produtividade.Phosphated fertilizers, such as superphosphate, triple superphosphate and monoamonium phosphate, applied throught drip irrigation can present pipe incrustations and emitters obstructions. In this research, carried out in the UNESP - São Paulo State University, Jaboticabal - Brazil, it was studied the phosphorous distribution, the influence on pH and the moisture in one Oxisoil, fertigated during one month, with five applications of phosphoric acid. Four replications and eight treatments were applied, and the treatments combined two rates of P2O5 (0 and 50 kg ha-1 and four frequencies of applications (1; 3; 5 and 7 days. The irrigation or fertigation frequency did not influence the distribution of the moisture in

  8. Encapsulation of strontium aluminate phosphors to enhance water resistance and luminescence

    International Nuclear Information System (INIS)

    Zhu Yong; Zeng Jianghua; Li Wenyu; Xu Li; Guan Qiu; Liu Yingliang

    2009-01-01

    Strontium aluminate SrAl 2 O 4 :Eu 2+ ,Dy 3+ phosphors are chemically unstable against water or even moisture. To enhance the water resistance of the phosphors, an encapsulation was performed by direct surface reactions with phosphoric acid (H 3 PO 4 ). The morphology, surface structure, surface element composition, water resistance, luminescence, and photoacoustic spectrum of the phosphors before and after encapsulation were discussed. Experimental results showed that phosphors were perfectly encapsulated by amorphous layers in nanoscale and crystalline layers in microscale under different conditions. The water resistance of phosphors was greatly enhanced by the two types of layer. More importantly, the amorphous layers enhanced the luminescence of phosphors markedly. The possible mechanism for the enhancements was also proposed.

  9. Preparation and characterization of a composite based on Zr(IV) and phosphoric acid; Preparacao e caracterizacao de um composito a base de Zr(IV) e acido fosforico

    Energy Technology Data Exchange (ETDEWEB)

    Silveira, T.F.S. da; Carmo, D.R. do, E-mail: taylafserantoni@gmail.com [Universidade Estadual Paulista Julio de Mesquita Filho (UNESP), Ilha Solteira, SP (Brazil). Faculdade de Engenharia. Departamento de Fisica e Quimica

    2014-07-01

    The present work describes the preparation and characterization of a composite formed from zirconium (IV) isopropoxide and phosphoric acid (ZrP). This composite (ZrP) was characterized by techniques such as infrared spectroscopy (FTIR), {sup 13}C and {sup 31}P nuclear magnetic resonance (NMR), X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS) and thermogravimetric analysis (TG). Vibrational spectrum for ZrP showed a band at ∼ 1010 cm{sup -1} assigned to the stretching P=O(νP=O). The results obtained by EDS confirmed the presence of elements Zr, P and O in the formed composite, and any C has been detected in concordance of NMR of {sup 13}C. The {sup 31}P NMR spectrum of ZrP showed two pronounced peaks characteristic of zirconium phosphate. In the TG curve three steps of weight loss were observed for ZrP. (author)

  10. Rare earths: critical elements for various applications and challenges in their separation

    International Nuclear Information System (INIS)

    Singh, D.K.; Chakravartty, J.K.

    2015-01-01

    High purity rare earths oxides, metal and alloys find wide applications in high tech area such as nuclear energy, permanent magnets, materials for storing hydrogen, phosphors, laser, etc. Rare earths consists a group of 15 elements from La to Lu in the periodic table and it also includes Sc and Y. Due to similar chemical nature owing to common oxidation state of +3, rare earths are very difficult to separate from each other. They have very low separation factors with acidic extractants like D2EHPA and EHEHPA and hence require large number of stages in various cascade of extraction process. Monazite (a source of rare earths, thorium and uranium) is processed at IREL to separate rare earths from thorium and uranium. The rare earths are fractionated into three groups namely light rare earths (LRE), middle rare earths (MRE) and heavy rare earths (HRE) by solvent extraction method employing EHEHPA as extractant

  11. Taxa de emissão de CO2 de um latossolo fertirrigado com ácido fosfórico por gotejamento CO2 emission rate from a fertigated bare soil with phosphoric acid by dripping

    Directory of Open Access Journals (Sweden)

    José R. Zanini

    2005-04-01

    Full Text Available A aplicação de fertilizantes fosfatados por meio de fertirrigação com sistemas de irrigação localizada pode causar obstrução de emissores. Para evitar esse problema, pode ser utilizado o ácido fosfórico como fonte de fósforo às plantas. Porém, têm sido pouco investigados os efeitos da irrigação relacionados às perdas de CO2 do solo para a atmosfera, em conseqüência da decomposição do carbono orgânico e da infiltração de água no solo. Neste trabalho, investigou-se, no período de um mês, o efeito da fertirrigação com ácido fosfórico nas taxas de emissão de CO2 de um latossolo desprovido de vegetação, na Área Experimental de Irrigação da UNESP, Câmpus de Jaboticabal - SP. Utilizou-se de um sistema de irrigação por gotejamento, com delineamento experimental em blocos casualizados, constando de cinco repetições e cinco tratamentos (0; 30; 60; 90 e 120 kg ha-1de P2O5, aplicados via fertirrigação com ácido fosfórico. Verificou-se que as taxas de emissão de CO2 aumentaram significativamente após as fertirrigações, porém não houve efeito da dose do ácido fosfórico sobre as taxas. A umidade do solo mostrou-se um fator importante na relação entre as variações das taxas de emissão e a temperatura do solo ao longo do período estudado.The application of phosphoric fertilizers through fertigation, with localized irrigation systems, can cause emitters obstruction. In order to avoid this problem, the phosphoric acid can be used as phosphorus source to the plants. However, it has been little investigations on the effects of the irrigation practices, related to the CO2 transference to the atmosphere, due to organic matter decomposition in the soil and its water infiltration. At this work, the rates of emissions of CO2 from a bare soil without vegetation, and fertigated along one month were investigated. The experiment was conducted with randomized blocks design in São Paulo State University - UNESP

  12. Improvements in phosphors

    International Nuclear Information System (INIS)

    Rabatin, J.G.

    1981-01-01

    For X-ray image converter applications, especially when used in medical radiography, it is desirable to improve the speed and brightness of response for conversion of X-rays in phosphors. The rare earth oxyhalide phosphors coactivated with a combination of rare earth activators described in this patent are capable of exhibiting low afterglow with high ultraviolet emission. They have the general formula Lnsub(1-y-w)OX:Tbsub(y)Tmsub(w) where Ln is lanthanum or gadolinium, X is chlorine and/or bromine, y is from 0.0005 to 0.010 moles per mole and w is from 0.00005 to 0.005 moles per mole of the Lnsub(1-y-w)OX host. The method of preparation and characteristics of speed, afterglow and UV emission are described. (U.K.)

  13. Thermodynamic and structural of the water - dodecane - bis(ethyl-2-hexyl) phosphoric acid and its sodium salt; Etude thermodynamique et structurale du systeme: eau - dodecane - acide bis(ethyl-2 hexyl) phosphorique et de son sel de sodium

    Energy Technology Data Exchange (ETDEWEB)

    Lovera, Jacqueline

    1985-12-20

    This research thesis reports the study of the appearance and disappearance of the 'third phase' obtained during the salification of the bis(ethyl-2 hexyl) phosphoric acid (HDEHP) diluted in dodecane, by sodium aqueous solutions. After a large bibliographical study on the properties of the intervening compounds (extraction of metallic cation by the acid, parameters influencing the 'third phase' appearance, surfactant properties, direct and inverse micelles, formation of para-crystalline phases), the author presents chemical experimental methods: liquid-liquid extraction tests, tests by the synthetic way, preparation of reactants, dosing method, methods of chemical analysis). Then, she reports and discusses experimental results in terms of determination of phase diagrams at 25 C, of composition by weight of the third phase, of influence of the apolar diluent, and of influence of the electrolyte. Physical experimental methods are then presented (differential calorimetric analysis, NMR, small angle X-ray scattering, light scattering, polarised light microscopy, constrained phase microscopy, photography, infrared spectroscopy, conductometry, transmission electron micrography, volumetric mass measurements, surface and interface tension measurements, viscoelasticity measurements) and their results are discussed and interpreted [French] Nous etudions l'apparition et la disparition de la 'troisieme phase' obtenue lors de la salification de l'acide bis(ethyl-2 hexyl) phosphorique - HDEHP - dilue dans le dodecane, par des solutions aqueuses de soude. Nous obtenons cinq resultats experimentaux essentiels: a - dans le systeme etudie, la troisieme phase n'apparait qu'au dela de la salification. La phase qui apparait est une phase aqueuse de soude diluee, se separant de la phase organique en equilibre avec le dodecane presente a la salification exacte. b - la disparition de la troisieme phase s'effectue par recombinaison des deux phases organiques: la 'phase organique lourde

  14. Removal of uranium(VI) from aqueous solutions by new phosphorus-containing carbon spheres synthesized via one-step hydrothermal carbonization of glucose in the presence of phosphoric acid

    International Nuclear Information System (INIS)

    Zhi-bin Zhang; East China Institute of Technology, Fuzhou; China University of Geosciences, Wuhan; Zhi-wei Zhou; Xiao-hong Cao; Yun-hai Liu; Guo-xuan Xiong; East China Institute of Technology, Fuzhou; Ping Liang; East China Institute of Technology, Fuzhou; China University of Geosciences, Wuhan

    2014-01-01

    The novel phosphorus-rich hydrothermal carbon spheres (HCSs-PO 4 ) have been synthesized via one-step hydrothermal carbonization of glucose in the presence of phosphoric acid. The textural and surface chemistry properties were characterized using Boehm titrations, scanning electron microscopy and Fourier transform infrared spectrometer. The content of oxygen-containing functional groups on the surface of HCSs increased from 0.053 to 1.009 mmol g -1 by phosphate group modification. The adsorption ability of HCSsPO 4 has been explored for the removal of uranium from aqueous solutions. The adsorption kinetic data were best described by the pseudo-second-order equation. Adsorption process could be well defined by the Langmuir isotherm, the adsorption capacity of HCSs increased from 80.00 to 285.70 mg g -1 after phosphate group modification. And thermodynamic parameters indicated the adsorption process was feasible,endothermic and spontaneous. Selective adsorption studies showed that the HCSs-PO 4 could selectively remove U(VI), and the selectivity coefficients had been improved in the presence of co-existing ions, Na(I), Ni(II), Sr(II), Mn(II), Mg(II) and Zn(II). Complete removal (99.9 %) of U(VI) from 1.0 L industry wastewater containing 15.0 mg U(VI) ions was possible with 12.0 g HCSs-PO 4 . (author)

  15. Achievement report for fiscal 1997 on joint research to develop fuel cell technologies for urban energy centers. Research on evaluating life of phosphoric acid fuel cells; 1997 nendo toshi energy center nado nenryo denchi gijutsu kaihatsu kyodo kenkyu seika hokokusho. Rinsangata nenryo denchi jumyo hyoka kenkyu

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-05-01

    This paper discusses life evaluation on phosphoric acid fuel cells of urban energy center type for regional energy supply and on-site type to be installed in buildings. Operation characteristics tests and disassembly checks allow to identify factors for voltage decrease, and estimate the life therefrom particularly if the voltage decrease is caused from catalyst activity. The time before 10% decrease value is reached is now about 40,000 hours. The creep analysis method that has been developed recently can predict deformation in full-size reformers nearly exactly, and is effective in operating the reformer and evaluating the life at the design stage. Creep buckling is the critical value, which is caused by ecliptic deformation of internal tubes in the second catalyst layer. In a heat exchanger for fuel gas preheating, carbon in the reformed gas is carbonized and deposited due to catalytic action of nickel in the brazing material that bonds plates and fins in the heat exchanger. Iron also has a possibility of performing catalytic action. In the on-site type 1,000-kW class fuel cells, no structural problems have been presented even after the operation has been stopped. In order to extend time interval between phosphoric acid supply into the cells, it is necessary to reduce difference in the remaining phosphoric acid amounts in the stack lamination direction and in the cell flat surface. (NEDO)

  16. Fiscal 1997 report on the results of the international standardization R and D. R and D of the standardization of a method to test acceleration life of phosphorous acid fuel cells; 1997 nendo seika hokokusho kokusai hyojun soseigata kenkyu kaihatsu. Rinsangata nenryo denchi no kasoku jumyo shiken hoho no hyojunka ni kansuru kenkyu kaihatsu

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-03-01

    As for fuel cells, which are expected as a new clean energy, the R and D are being proceeded with in various fields of the world, but the standardization has not been made both in Japan and abroad. In Japan, the situation is that the information on technical terms, indication method, performance test method, and environment/safety test methods of the phosphorous acid fuel cell power generation is publicly spread. In relation to the international promotion of fuel cells to be predicted, it is necessary to internationally standardize cells themselves which are a key component of fuel cell power generation facilities. Phosphorous acid fuel cells are expected of the earliest commercialization of all, but the common test method to evaluate life characteristics of the cell stack has not been established yet. In the R and D, for the purpose of internationally standardizing test methods to evaluate life characteristics of the cell stack, a study on the acceleration life test method of phosphoric acid fuel cells was conducted in terms of the technical trend, data, standard, etc. A plan was prepared on general rules of the method to test acceleration life at the cell reaction part of the small cell, and activities also were started for setting up a technical committee for the fuel cell power system in President`s Advisory Committee on Future Technology. 29 figs., 20 tabs.

  17. Study of phosphorous based resins for the uptake of plutonium from H2SO4 based analytical waste

    International Nuclear Information System (INIS)

    Seshadri, H.; Mohandas, Jaya; Srinivasan, S.; Kumar, T.; Rajan, S.K.

    2006-01-01

    This study indicates that phosphorous based resins can be conveniently employed for the uptake of plutonium from analytical wastes even in strong acid media and also in the presence of diverse ions like silver and chromium. It is also evident that phosphorous based resins have proved to be efficient even in sulphuric acid medium

  18. Industrial radiography with phosphor screens

    International Nuclear Information System (INIS)

    Broadhead, P.

    1981-01-01

    An experimental system that comprises a film of low silver content and a pair of high resolution phosphor intensifying screens and a commercial industrial X-ray film of similar speed are compared for image quality. It is concluded that the use of phosphor screens offers an increase in image quality when the information is limited by the graininess or quantum mottle of a radiograph which is frequently the case in practical radiography. (author)

  19. Electron-beam-pumped phosphors

    International Nuclear Information System (INIS)

    Goldhar, J.; Krupke, W.F.

    1985-01-01

    Electron-beam excitation of solid-state scintillators, or phosphors, can result in efficient generation of visible light confined to relatively narrow regions of the spectrum. The conversion efficiency can exceed 20%, and, with proper choice of phosphors, radiation can be obtained anywhere from the near infrared (IR) to the near ultraviolet (UV). These properties qualify the phosphors as a potentially useful pump source for new solid-state lasers. New phosphors are being developed for high-brightness television tubes that are capable of higher power dissipation. Here, an epitaxial film of fluorescing material is grown on a crystalline substrate with good thermal properties. For example, researchers at North American Philips Laboratories have developed a cerium-doped yttrium aluminum garnet (YAG) grown on a YAG substrate, which has operated at 1 A/cm 2 at 20 kV without observed thermal quenching. The input power is higher by almost two orders of magnitude than that which can be tolerated by a conventional television phosphor. The authors describe tests of these new phosphors

  20. Formation of rod type structures of CaSO4: Ce,P,Dy TLD phosphor using different synthesis routes

    International Nuclear Information System (INIS)

    Atone, M.S.; Wani, J.A.; Dhoble, S.J.

    2011-01-01

    Effect of Ce and P co-activation in CaSO 4 : Dy, standard TLD phosphor prepared by different synthesis root techniques and it's structural morphology is reported first time in this paper. We have already reported the sensitization of luminescence in CaSO 4 : Dy with phosphorous (P) and cerium (Ce) ions separately via acid distillation route. In the current investigation, we have doped these impurities (Ce, P, Dy) simultaneously in CaSO 4 host lattice. We have employed a well known chemical precipitation method and modified acid distillation method and have attempted to analyse the surface morphology resulted from these two synthesis routes. Chemical precipitation usually takes place at room temperature and in this way allows the reaction to take place silently. In case of acid distillation method we have reduced the synthesis temperature to 493K which is considerably less than 653K employed in previously reported literature. In case of precipitation method particle shape seems to be spherical and particle size is around one micro range or in the neighbourhood of nanorange. However, in the case of modified acid distillation method particles have shaped in to rod like structures and particle size again falls in the micro range. The photoluminescence intensity of the phosphor prepared by chemical precipitation method is weak as compared to the phosphor prepared by modified acid distillation method. Both the phosphors prepared by different methods have shown characteristic transitions of dopants. The emission spectra of prepared phosphors at 309 nm and 329 nm of Ce 3+ ions overlap well with excitation of Dy 3+ ions. Thermoluminescence (TL) property of both phosphors is again good though certain variation is observed in case of phosphor prepared by modified acid distillation method which shows rod like structure of phosphor. This variation in TL may be attributed to change in surface morphology (formation of rod type structure of particles) of the phosphor. (author)

  1. Studies on supercritical fluid extraction of uranium from sodium diuranate

    International Nuclear Information System (INIS)

    Prabhat, Parimal; Vithal, G.K.; Rao, Ankita; Kumar, Pradeep; Tomar, B.S.

    2014-01-01

    Crude sodium diuranate (SDU) produced from phosphoric acid by solvent extraction process with di-2-ethyl hexyl phosphoric acid (D2EHPA) and tri-n-butyl phosphate(TBP) contains iron and other rare earth impurities along with uranium. For further use of this uranium for fuel fabrication and its subsequent use in nuclear reactors, it has to be purified up to nuclear grade ammonium diuranate (ADU) specifications. Conventionally crude SDU is being purified by dissolving it in nitric acid followed by solvent extraction process using TBP in diluent. Use of large amount of acid and organic solvents for industrial processes is an environmental concern. Nowadays there are efforts to minimize use of acid and organic solvents in industrial processes. Supercritical Fluid Extraction (SFE) of uranium from different matrices (solid as well as liquid) has been reported by several authors in recent years. Near complete extraction of uranium from UO 2 (powder, green pellet and sintered pellet) using TBP-HNO 3 adduct by SFE has been reported. We attempted to explore possibility to purify crude SDU to nuclear grade by SFE of uranium from crude SDU matrix and study the effect of different operational parameters, mode of extraction and complexation

  2. Radioluminescent nuclear batteries with different phosphor layers

    International Nuclear Information System (INIS)

    Hong, Liang; Tang, Xiao-Bin; Xu, Zhi-Heng; Liu, Yun-Peng; Chen, Da

    2014-01-01

    Highlights: • We present and test the electrical properties of the nuclear battery. • The best thickness range for ZnS:Cu phosphor layer is 12–14 mg cm −2 for 147 Pm radioisotope. • The best thickness range for Y 2 O 2 S:Eu phosphor layer is 17–21 mg cm −2147 Pm radioisotope. • The battery with ZnS:Cu phosphor layer can provide higher energy conversion efficiency. • The mechanism affecting the nuclear battery output performance is revealed. - Abstract: A radioluminescent nuclear battery based on the beta radioluminescence of phosphors is presented, and which consists of 147 Pm radioisotope, phosphor layers, and GaAs photovoltaic cell. ZnS:Cu and Y 2 O 2 S:Eu phosphor layers for various thickness were fabricated. To investigate the effect of phosphor layer parameters on the battery, the electrical properties were measured. Results indicate that the optimal thickness ranges for the ZnS:Cu and Y 2 O 2 S:Eu phosphor layers are 12 mg cm −2 to 14 mg cm −2 and 17 mg cm −2 to 21 mg cm −2 , respectively. ZnS:Cu phosphor layer exhibits higher fluorescence efficiency compared with the Y 2 O 2 S:Eu phosphor layer. Its spectrum properly matches the spectral response of GaAs photovoltaic cell. As a result, the battery with ZnS:Cu phosphor layer indicates higher energy conversion efficiency than that with Y 2 O 2 S:Eu phosphor layer. Additionally, the mechanism of the phosphor layer parameters that influence the output performance of the battery is discussed through the Monte Carlo method and transmissivity test

  3. Phosphorous loads evaluation from soil

    International Nuclear Information System (INIS)

    Mezzanotte, V.

    1996-01-01

    With reference to the well known difficulty of quantifying non point phosphorous loads, as well as to their growing relative importance where point source leads decrease, a literature review has been carried out concerning soil export coefficients. On such basis, the values which seem to be the most appropriate for Italy have been estimated for different land use categories. The main mechanisms determining non point phosphorous load generation and the factors affecting their importance are also described. In the end, criteria for estimating the importance of non point sources in a basin are suggested to be used for deciding whether a traditional, parametric assessment (inevitably involving a certain error) can be acceptable or experimental measures are needed

  4. General report on the results of the development of fuel cell technology such as urban energy center. Evaluation study of life of phosphoric acid fuel cells (fiscal 1995 and 1996); Toshi energy center nado nenryo denchi gijutsu kaihatsu kenkyu seika sogo hokokusho. Rinsangata nenryo denchi jumyo hyoka kenkyu (1995 kara 1996 nendo)

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-03-01

    Receiving subsidies from MITI, NEDO carried out this project in fiscal 1995 and 1996 as a joint research with Technology Research Association for Phosphoric Acid Fuel Cell Power Generation System and others. The project aimed at developing the accelerated test method which can evaluate in a short time the cell life of phosphoric acid fuel cells (PAFC) and the lowering of characteristics. The accelerated test method of PAFC life is thought to be a tool indispensable for the promotion of commercialization, but the accelerated test method like the usual material evaluation has not yet been established. To solve this problem, procedures were developed to rationally plan the accelerated test on short stacks of full scale based on the small cell test data. Here, to rationally estimate the operational state under actual conditions based on the data on the accelerated test, it is necessary to fully understand the mechanism of deterioration of PAFC. By conducting in parallel the element study for the basic elucidation of cell deterioration phenomena, obtained was the useful information/knowledge which back up the results of the accelerated test scientifically. 168 figs., 33 tabs.

  5. Luminescence studies on phosphor screens

    International Nuclear Information System (INIS)

    Panayiotakis, G.; Nomikos, C.; Bakas, A.; Proimos, B.

    1994-01-01

    We report our results on x-ray phosphor screens prepared of some new materials focusing attention on their efficiency under fluoroscopy conditions, on optimization conditions and on comparisons among the various materials. All data are presented in absolute values. A theoretical model is presented, that takes into account the granular structure of the screens, permitting the explanation and prediction of the luminescence properties of the screens. (authors)

  6. Luminescence studies on phosphor screens

    Energy Technology Data Exchange (ETDEWEB)

    Panayiotakis, G; Nomikos, C; Bakas, A; Proimos, B [Medical Physics Department, University of Patras, 265 00 Patras, Greece (Greece)

    1994-12-31

    We report our results on x-ray phosphor screens prepared of some new materials focusing attention on their efficiency under fluoroscopy conditions, on optimization conditions and on comparisons among the various materials. All data are presented in absolute values. A theoretical model is presented, that takes into account the granular structure of the screens, permitting the explanation and prediction of the luminescence properties of the screens. (authors). 12 refs, 3 figs.

  7. Quality parameters evaluation for the determination of available phosphorous in soils

    International Nuclear Information System (INIS)

    Garcia Galvis, John Brynner; Ballesteros, Maria Ines

    2006-01-01

    There are some colorimetric procedures for determining available phosphorous in soils, and phosphorous is evaluated by means of a blue complex (phosphomolybdic acid); in one of the methods, color appear when ascorbic acid is used as reductor agent, and in the other when stannous chloride is used. Both methods use the same extractive solution bray i i due to its good response for acid soil cultures, like most Colombian soils are. When the two methodologies were compared it was found that the most sensible method and with the best limit of detection and quantification was the one that uses ascorbic acid, antimonious and potassium tartrate. Its variation coefficients and standard deviation were lower, and for this reason it is considered as the most precise method for phosphorous determination

  8. The sealing of second mandibular temporary molar pits and fissure with the laser of Nd: YAG, phosphoric acid and the glass ionomer cement; Selamento de fossulas e fissura de segundo molar deciduo inferior com laser de Nd: YAG, acido fosforico e cimento de ionomero de vidro

    Energy Technology Data Exchange (ETDEWEB)

    Toda, Maria Aparecida

    2003-07-01

    The main of our study was to check the sealing of second mandibular temporary molar pits and fissure, in vitro, with the laser of Nd: YAG, phosphoric acid at 37% and the glass ionomer cement (CIV, Fuji IX GC).The proposal was to check the structural morphologic changes in the laser irradiation upon the enamel surface to watch the pits and fissure sealing with the glass ionomer cement use after the laser irradiation and to verify the efficiency of the 'double conditioning' (phosphoric acid + Nd: YAG). At the same time we watch the evolution of the temperature in the pulp chamber's inside. Our desire was to achieve a therapeutic alternative technic to prevent the dental caries. The Nd: YAG laser parameters were the same: 79 mJ of energy per pulse; frequency of 5 Hz; mean power of 0,4 W; optical fiber on contact of 320 {mu}m diameter; fluency of 99,52 J/ cm{sup 2}, assuming that the only differential was the time of the laser application on the enamel surface. The samples were prepared with this way: Laser Nd: YAG (53 second) + acid + CIV (Fuji IX); Laser Nd: YAG (53 s); Laser Nd: YAG (20 s + 20 s) + acid + CIV; Laser Nd: YAG (20 s + 20 s); Acid + CIV; Control. Through the scanning electron microscopy (MEV) we noticed fusion and resolidification regions due to the laser irradiation and a better adaptation of the glass ionomer cement when we did the 'double conditioning'. Concerning the temperature increase we can conclude that the echeloned period was the best recommended because the temperature was found in a pattern that would not cause any damage to the dental pulp. For future studies we suggest a longer relaxing time between the laser irradiation, a comparative study of this method with other lasers, the use of other sealing materials and the study with the permanent teeth. (author)

  9. The sealing of second mandibular temporary molar pits and fissure with the laser of Nd: YAG, phosphoric acid and the glass ionomer cement; Selamento de fossulas e fissura de segundo molar deciduo inferior com laser de Nd: YAG, acido fosforico e cimento de ionomero de vidro

    Energy Technology Data Exchange (ETDEWEB)

    Toda, Maria Aparecida

    2003-07-01

    The main of our study was to check the sealing of second mandibular temporary molar pits and fissure, in vitro, with the laser of Nd: YAG, phosphoric acid at 37% and the glass ionomer cement (CIV, Fuji IX GC).The proposal was to check the structural morphologic changes in the laser irradiation upon the enamel surface to watch the pits and fissure sealing with the glass ionomer cement use after the laser irradiation and to verify the efficiency of the 'double conditioning' (phosphoric acid + Nd: YAG). At the same time we watch the evolution of the temperature in the pulp chamber's inside. Our desire was to achieve a therapeutic alternative technic to prevent the dental caries. The Nd: YAG laser parameters were the same: 79 mJ of energy per pulse; frequency of 5 Hz; mean power of 0,4 W; optical fiber on contact of 320 {mu}m diameter; fluency of 99,52 J/ cm{sup 2}, assuming that the only differential was the time of the laser application on the enamel surface. The samples were prepared with this way: Laser Nd: YAG (53 second) + acid + CIV (Fuji IX); Laser Nd: YAG (53 s); Laser Nd: YAG (20 s + 20 s) + acid + CIV; Laser Nd: YAG (20 s + 20 s); Acid + CIV; Control. Through the scanning electron microscopy (MEV) we noticed fusion and resolidification regions due to the laser irradiation and a better adaptation of the glass ionomer cement when we did the 'double conditioning'. Concerning the temperature increase we can conclude that the echeloned period was the best recommended because the temperature was found in a pattern that would not cause any damage to the dental pulp. For future studies we suggest a longer relaxing time between the laser irradiation, a comparative study of this method with other lasers, the use of other sealing materials and the study with the permanent teeth. (author)

  10. Method of preparing a thermoluminescent phosphor

    Science.gov (United States)

    Lasky, Jerome B.; Moran, Paul R.

    1979-01-01

    A thermoluminescent phosphor comprising LiF doped with boron and magnesium is produced by diffusion of boron into a conventional LiF phosphor doped with magnesium. Where the boron dopant is made to penetrate only the outer layer of the phosphor, it can be used to detect shallowly penetrating radiation such as tritium beta ays in the presence of a background of more penetrating radiation.

  11. Phosphors for X-ray intensification screens

    International Nuclear Information System (INIS)

    Rebatin, J.G.

    1980-01-01

    An improved rare earth oxyhalide phosphor for x-ray intensification screens is described. The phosphors, of formula LnOX.T where Ln = La or Gd, X = Cl or Br and T = Tm or Tb, are mixed with a small amount of a trivalent antimony compound. The addition of antimony overcomes ageing due to attack by atmospheric moisture and renders the phosphor freeflowing so that dispersions can be readily made. Preferably the phosphor is washed with an aqueous solution of the antimony compound and the compound is the fluoride, chloride or butoxide, or potassium antimony tartrate. (U.K.)

  12. Chemical process for recovery of uranium values contained in phosphoric mineral lixivia

    International Nuclear Information System (INIS)

    Conceicao, E.L.H. da; Awwal, M.A.; Coelho, S. V.

    1980-01-01

    A recovery process of uranium values from phosporic mineral lixivia for obtaining uranio oxide concentrate adjusted to specifications of purity for its commercialization the process consists of the adjustment of electromotive force of lixiviem to suitable values for uranium extraction, extraction with organic solvent containing phosphoric acid ester and oxidant reextraction from this solvent with phosphoric acid solution, suggesting a new solvent extraction containing synergetic mixture of di-2-ethyl hexyl phosphoric acid and tri-octyl phosphine, leaching this solvent with water and re-extraction/precipitation with ammonium carbonate solution, resulting in the formation of uranyl tricarbonate and ammonium, that by drying and calcination gives the uranium oxide with purity degree for commercialization. (M.C.K.) [pt

  13. Towards zero discharge by integrated effluent treatment approach

    International Nuclear Information System (INIS)

    Rath, Ashish Kumar; Pattnaik, Sambhu Prasad; Pati, Ganeswar; Saha, Sushant; Viswanath, Kowtha

    2014-01-01

    Heavy Water Plant, Talcher houses two Organo-phosphorus Solvent Production Plants namely, 60 MTPY TBP Plant engaged in the production of Tri-n-Butyl Phosphate and Versatile Solvent Production Plant (VSPP) capable of producing various Organo Phosphorus Solvents namely, 100 MTPY D2EHPA (Di-2-Ethyl Hexyl Phosphoric Acid), or 40 MTPY TAPO (Tri-Alkyl Phosphine Oxide) or TOPO (Tri-n-Octyl Phosphine Oxide) or DNPPA (Di-Nonyl Phenyl Phosphoric Acid). These solvents have important application for separation duties in front and back end of nuclear fuel cycle and also in conventional hydrometallurgy for separation metals like Ni, Cu, Zn, Co etc., both of these plants are first of their kind in India designed by the Heavy Water Board, Mumbai with R and D inputs from BARC. The two plants employ esterification (1) process between PCl 3 / and a suitable oxo-alcohol followed by hydrolysis, neutralization and product purification. The second and third steps find large usage of Water, which eventually surface as liquid effluent. All the gaseous emissions from plants, mostly HCl gas are traded off for Saline Water as liquid effluent by scrubbing the same with Sodium Hydroxide Solution

  14. Remoção de chumbo(II em sistemas descontínuos por carvões ativados com ácido fosfórico e com vapor Lead(II removal in discontinous systems by carbon activated by phosphoric acid and vapor

    Directory of Open Access Journals (Sweden)

    Cristiane Imenes de Campos Bueno

    2007-01-01

    Full Text Available Adsorption of heavy metal cations by activated carbon is dependent on the capacity of the material in promoting adsorption and the time needed to reach equilibrium. Carbon samples were previously activated either by phosphoric acid treatment at 400 ºC or by steam at 800 ºC. The results of Pb(II adsorption by these activated carbons have shown that equilibrium was typically reached within the first 5 min of contact between carbon and metal solution, with a maximum adsorption capacity higher than 69 mg g-1 for the vapor-activated sample. Temperature influences the sorption capacity, which corresponds to an endothermic process. Lead(II retention is more pronounced at high temperature and low pH.

  15. Molecular and supramolecular speciations of solvent extraction systems based on malonamide and/or dialkyl-phosphoric acids for An(III)/Ln(III); Speciations moleculaire et supramoleculaire de systemes d'extraction liquide-liquide a base de malonamide et/ou d'acides dialkylphosphoriques pour la separation An(III)/Ln(III)

    Energy Technology Data Exchange (ETDEWEB)

    Gannaz, B

    2006-06-15

    The solvent extraction system used in the DIAMEX-SANEX process, developed for the actinide(III)/lanthanide(III) separation, is based on the use of mixtures of the malonamide DMDOHEMA and a dialkyl-phosphoric acid (HDEHP or HDHP), in hydrogenated tetra-propylene. The complexity of these systems urges on a novel approach to improve the conventional methods (thermodynamics, solvent extraction) which hardly explain the macroscopic behaviors observed (3. phase, over-stoichiometry). This approach combines studies on both supramolecular (VPO, SANS, SAXS) and molecular (liquid-liquid extraction, ESI-MS, IR, EXAFS) speciations of single extractant systems (DMDOHEMA or HDHP in in n-dodecane) and their mixture. In spite of safety constraints due to the handling of radio-material, they were used in the studies as much as possible, like for SAXS measurements on americium-containing samples, a worldwide first-time. In each of the investigated systems, actinides(III) and lanthanides(III) are extracted to the organic phase in polar cores of reversed micelles, the inner and outer-sphere compositions of which are proposed. Thus, the 4f and 5f cations are extracted by reversed micelles such as [(DMDOHEMA){sub 2}M(NO{sub 3}){sub 3}]{sub inn} (DMDOHEMA){sub x}(HNO{sub 3}){sub z}(H{sub 2}O){sub w}]{sub out} and M(DHP){sub 3}(HDHP){sub y-3}(H{sub 2}O){sub w} with y = 3 to 6, for the single extractant systems. In the case of the two extractants system, the less concentrated one acts like a co-surfactant regarding the mixed aggregate formation [(DMDOHEMA){sub 2}M(NO{sub 3}){sub 3-v}(DHP){sub v}]{sub inn} [(DMDOFIEMA){sub x}(HDHP){sub y}(HNO{sub 3})z(H{sub 2}O){sub w}]{sub out}. (author)

  16. Study on the kinetics of high-energy phosphates in myocardium by phosphorous nuclear magnetic resonance

    Energy Technology Data Exchange (ETDEWEB)

    Kusuoka, Hideo; Tsuneoka, Yutaka; Inoue, Michitoshi; Abe, Hiroshi [Osaka Univ. (Japan). Faculty of Medicine; Watari, Hiroshi

    1982-12-01

    Effect of artificial blood, FC 43 (Perfluorochemicals) on the kinetics of high-energy phosphate in the myocardium was evaluated by /sup 31/P-NMR which permits a continuous and non-invasive assessment of in vivo phosphorus compounds. Cardiac perfusion was carried out on a excised rat heart with a Krebs-Henseleit modified solution and FC 43 alternately. Under the normal condition, ischemic condition, and at second perfusion amounts of intramyocardial creatine phosphoric acid, ATP, and inorganic phosphorus were determined by /sup 31/P-NMR. Coronary flow was simultaneously estimated. The ischemic state due to interruption of perfusion resulted in a decrease in creatine phosphoric acid, which was associated with an increase in inorganic phosphorus and intracellular acidosis. No change of ATP amount was observed under ischemic state. With resumption of perfusion, the levels of creatine phosphoric acid and inorganic phosphorus rapidly returned to the normal. In the group of FC 43, coronary flow was 2.68 ml/min/g of the heart weight, about 1/2 of that of the Krebs-Henseleit group (5.68 ml/min/g of the heart weight). In controls, there was no difference between the two groups concerning creatine phosphoric acid level and recovery of creatine phospohric acid level after ischemia. These results showed that FC 43 supplies sufficient oxygen, and has no effect on the kinetics of energy in the myocardium.

  17. Phosphorous-Containing Polymers for Regenerative Medicine

    Science.gov (United States)

    Watson, Brendan M.; Kasper, F. Kurtis; Mikos, Antonios G.

    2014-01-01

    Disease and injury have resulted in a large, unmet need for functional tissue replacements. Polymeric scaffolds can be used to deliver cells and bioactive signals to address this need for regenerating damaged tissue. Phosphorous-containing polymers have been implemented to improve and accelerate the formation of native tissue both by mimicking the native role of phosphorous groups in the body and by attachment of other bioactive molecules. This manuscript reviews the synthesis, properties, and performance of phosphorous-containing polymers that can be useful in regenerative medicine applications. PMID:24565855

  18. Transuranium removal from Hanford high level waste simulants using sodium permanganate and calcium

    International Nuclear Information System (INIS)

    Wilmarth, W.R.; Rosencrance, S.W.; Nash, C.A.; Fonduer, F.F.; Di Pirete, D.P.; Di Prete, C.C.

    2000-01-01

    Plutonium and americium are present in the Hanford high level liquid waste complexant concentrate (CC) due to the presence of complexing agents including di-(2-ethylhexyl) phosphoric acid (D 2 EHPA), tributylphosphate (TBP), hydroxyethylene diamine triacetic acid (HEDTA), ethylene diamine tetraacetic acid (EDTA), citric acid, glycolic acid, and sodium gluconate. The transuranic concentrations approach 600 nCi/g and require processing prior to encapsulation into low activity glass. BNFL's (British Nuclear Fuels Limited's) original process was a ferric co-precipitation method based on earlier investigations by Herting and Orth, et al. Furthermore, flocculation and precipitation are widely used for clarification in municipal water treatment. Co-precipitation of Np, Am, and Pu with ferric hydroxide is also used within an analytical method for the sum of those analytes. Tests to evaluate BNFL's original precipitation process indicated the measured decontamination factors (DFs) and filter fluxes were too low. Therefore, an evaluation of alternative precipitation agents to replace ferric ion was undertaken. Agents tested included various transition metals, lanthanide elements, uranium species, calcium, strontium, and permanganate

  19. Fluorimetrich determination of uranium in mineral samples and phosphoric solutions

    International Nuclear Information System (INIS)

    Pupo Gonzales, I.; Cuevillas, J.; Estevez, J.

    1991-01-01

    In this paper an analytical technique for the determination of uranium in different cuban minerals and acid leaching liquors of phosphorites is proposed. The method used for solid samples includes their disolution and further dilution of the solution obtained. For liquid samples dilution is the only intermediate step used. A study of HNO3 concentration (pH) was made in fluorimetric measurements. The method was applied to the uranium analysis in two IAEA standard reference samples (phosphate base), in natural phosphorites and a synthetic one, in clays and phosphoric liquors. The results agree with those obtained by other methods

  20. Improvements in x-ray image converters and phosphors

    International Nuclear Information System (INIS)

    Rabatin, J.G.

    1981-01-01

    Improvements to an X-ray image converter comprising crystals of rare earth phosphor admixtures are described. The phosphor admixtures utilize thulium-activated lanthanum and/or gadolinium oxyhalide phosphor material to increase the relative speed and resolution of an X-ray image compared with conventional rare earth phosphors. Examples of various radiographic screens containing one or more of the phosphor materials are given. (U.K.)

  1. Characteristics of the Panasonic UD-802 phosphors

    International Nuclear Information System (INIS)

    Ben-Shachar, B.; Catchen, G.L.; Hoffman, J.M.

    1989-01-01

    Several basic dosimetric characteristics of Li 2 B 4 O 7 :Cu and CaSO 4 :Tm phosphors in Panasonic UD-802 dosemeters were measured. The TL dose response linearity was determined over the useful range of personnel and environmental dosimetry (0.005 - 10 mGy), and the minimum measurable doses were calculated. The intrinsic ultraviolet (UV) radiation sensitivity of both phosphors was checked before and after γ irradiation for the purpose of re-assessing high doses. The results indicate that Li 2 B 4 O 7 :Cu is UV sensitive and, therefore, re-assessment is not applicable. Although the CaSO 4 :Tm phosphor exhibited UV sensitivity after γ irradiation, the results were not consistent with those reported earlier and more study is required. The fading of both phosphors was evaluated in Panasonic UD-801 dosemeters for periods up to 90 days. (author)

  2. Phosphate Phosphors for Solid-State Lighting

    CERN Document Server

    Shinde, Kartik N; Swart, H C; Park, Kyeongsoon

    2012-01-01

    The idea for this book arose out of the realization that, although excellent surveys and a phosphor handbook are available, there is no single source covering the area of phosphate based phosphors especially for lamp industry. Moreover, as this field gets only limited attention in most general books on luminescence, there is a clear need for a book in which attention is specifically directed toward this rapidly growing field of solid state lighting and its many applications. This book is aimed at providing a sound introduction to the synthesis and optical characterization of phosphate phosphor for undergraduate and graduate students as well as teachers and researchers. The book provides guidance through the multidisciplinary field of solid state lighting specially phosphate phosphors for beginners, scientists and engineers from universities, research organizations, and especially industry. In order to make it useful for a wide audience, both fundamentals and applications are discussed, together.

  3. Fluorescent lighting with aluminum nitride phosphors

    Science.gov (United States)

    Cherepy, Nerine J.; Payne, Stephen A.; Seeley, Zachary M.; Srivastava, Alok M.

    2016-05-10

    A fluorescent lamp includes a glass envelope; at least two electrodes connected to the glass envelope; mercury vapor and an inert gas within the glass envelope; and a phosphor within the glass envelope, wherein the phosphor blend includes aluminum nitride. The phosphor may be a wurtzite (hexagonal) crystalline structure Al.sub.(1-x)M.sub.xN phosphor, where M may be drawn from beryllium, magnesium, calcium, strontium, barium, zinc, scandium, yttrium, lanthanum, cerium, praseodymium, europium, gadolinium, terbium, ytterbium, bismuth, manganese, silicon, germanium, tin, boron, or gallium is synthesized to include dopants to control its luminescence under ultraviolet excitation. The disclosed Al.sub.(1-x)M.sub.xN:Mn phosphor provides bright orange-red emission, comparable in efficiency and spectrum to that of the standard orange-red phosphor used in fluorescent lighting, Y.sub.2O.sub.3:Eu. Furthermore, it offers excellent lumen maintenance in a fluorescent lamp, and does not utilize "critical rare earths," minimizing sensitivity to fluctuating market prices for the rare earth elements.

  4. Luminescence Studies on Lamp Phosphors

    Energy Technology Data Exchange (ETDEWEB)

    Nagpal, J.S.; Godbole, S.V.; Varadharajan, G.; Page, A.G

    1998-07-01

    Photoluminescence and thermoluminescence of cerium magnesium aluminate CeMgAl{sub 11}O{sub 17}(Eu,Tb) and calcium halophosphate Ca{sub 5}(PO{sub 4}){sub 3}(F,Cl):Mn,Sb, two fluorescent materials currently in use for the commercial production of lamps in India, have been studied for possible applications in radiation and ultraviolet dosimetry. Cerium magnesium aluminate is highly sensitive to the visible spectral region. It has a linear response to 254 nm UV radiation over a wide range. Its UV sensitivity is significantly higher as compared to that of other known phosphors; however, its UV response is rate-dependent and may not play a significant role in UV dosimetry. Photoluminescence of CeMg aluminate is characteristic of Eu{sup 2+} and Tb{sup 3+} dopants, whereas the thermoluminescence emission of the UV irradiated powder at room temperature is dominated by Eu{sup 2+} dopant. Calcium halophosphate is insensitive to room lights, has a linear gamma response over 0.2-10{sup 2} Gy and may be useful in the case of radiation accidents. (author)

  5. Luminescence Studies on Lamp Phosphors

    International Nuclear Information System (INIS)

    Nagpal, J.S.; Godbole, S.V.; Varadharajan, G.; Page, A.G.

    1998-01-01

    Photoluminescence and thermoluminescence of cerium magnesium aluminate CeMgAl 11 O 17 (Eu,Tb) and calcium halophosphate Ca 5 (PO 4 ) 3 (F,Cl):Mn,Sb, two fluorescent materials currently in use for the commercial production of lamps in India, have been studied for possible applications in radiation and ultraviolet dosimetry. Cerium magnesium aluminate is highly sensitive to the visible spectral region. It has a linear response to 254 nm UV radiation over a wide range. Its UV sensitivity is significantly higher as compared to that of other known phosphors; however, its UV response is rate-dependent and may not play a significant role in UV dosimetry. Photoluminescence of CeMg aluminate is characteristic of Eu 2+ and Tb 3+ dopants, whereas the thermoluminescence emission of the UV irradiated powder at room temperature is dominated by Eu 2+ dopant. Calcium halophosphate is insensitive to room lights, has a linear gamma response over 0.2-10 2 Gy and may be useful in the case of radiation accidents. (author)

  6. MULTI-PHOTON PHOSPHOR FEASIBILITY RESEARCH

    Energy Technology Data Exchange (ETDEWEB)

    R. Graham; W. Chow

    2003-05-01

    Development of multi-photon phosphor materials for discharge lamps represents a goal that would achieve up to a doubling of discharge (fluorescent) lamp efficacy. This report reviews the existing literature on multi-photon phosphors, identifies obstacles in developing such phosphors, and recommends directions for future research to address these obstacles. To critically examine issues involved in developing a multi-photon phosphor, the project brought together a team of experts from universities, national laboratories, and an industrial lamp manufacturer. Results and findings are organized into three categories: (1) Multi-Photon Systems and Processes, (2) Chemistry and Materials Issues, and (3) Concepts and Models. Multi-Photon Systems and Processes: This category focuses on how to use our current understanding of multi-photon phosphor systems to design new phosphor systems for application in fluorescent lamps. The quickest way to develop multi-photon lamp phosphors lies in finding sensitizer ions for Gd{sup 3+} and identifying activator ions to red shift the blue emission from Pr{sup 3+} due to the {sup 1}S{sub 0} {yields} {sup 1}I{sub 6} transition associated with the first cascading step. Success in either of these developments would lead to more efficient fluorescent lamps. Chemistry and Materials Issues: The most promising multi-photon phosphors are found in fluoride hosts. However, stability of fluorides in environments typically found in fluorescent lamps needs to be greatly improved. Experimental investigation of fluorides in actual lamp environments needs to be undertaken while working on oxide and oxyfluoride alternative systems for backup. Concepts and Models: Successful design of a multi-photon phosphor system based on cascading transitions of Gd{sup 3+} and Pr{sup 3+} depends critically on how the former can be sensitized and the latter can sensitize an activator ion. Methods to predict energy level diagrams and Judd-Ofelt parameters of multi

  7. Green synthetic strategy of BCNO nanostructure and phosphor-based light – Emitting diodes

    Energy Technology Data Exchange (ETDEWEB)

    Kang, Yue [The Quartermaster Research Institute of General Logistics Department, Beijing 100010 (China); Yuan, Bo [Chemical Defense Institute of China, Beijing 100010 (China); Zhang, Dongjiu [Key Laboratory of Space Launching Site Reliability Technology, Hainan 570100 (China); Ma, Tian; Huang, Xiancong [The Quartermaster Research Institute of General Logistics Department, Beijing 100010 (China); Chu, Zengyong [College of Science, National University of Defense Technology, Changsha 410073 (China); Lai, Kan [The Quartermaster Research Institute of General Logistics Department, Beijing 100010 (China)

    2016-11-15

    BCNO phosphor has been paid much attention due to their unique physical, electronic and optical properties. Here we have successfully obtained BCNO nano-particle phosphor by microwave treating from boric acid, urea, and glucose at low temperatures and in short reaction time. Glucose decomposed into graphene quantum dots (GQDs), which facilitated the formation of hexagonal boron nitride (h-BN). Through our method, GQDs domains were uniformly incorporated into h-BN, leading to the formation of BCNO and decrease of bandgap. BCNO demonstrated excellent performance in light emitting diodes (LEDs) with green and blue light. We envision that this BCNO phosphor will enable the next generation blue and green LED devices due to the easiness of large scale fabrication at an economic cost.

  8. Green synthetic strategy of BCNO nanostructure and phosphor-based light – Emitting diodes

    International Nuclear Information System (INIS)

    Kang, Yue; Yuan, Bo; Zhang, Dongjiu; Ma, Tian; Huang, Xiancong; Chu, Zengyong; Lai, Kan

    2016-01-01

    BCNO phosphor has been paid much attention due to their unique physical, electronic and optical properties. Here we have successfully obtained BCNO nano-particle phosphor by microwave treating from boric acid, urea, and glucose at low temperatures and in short reaction time. Glucose decomposed into graphene quantum dots (GQDs), which facilitated the formation of hexagonal boron nitride (h-BN). Through our method, GQDs domains were uniformly incorporated into h-BN, leading to the formation of BCNO and decrease of bandgap. BCNO demonstrated excellent performance in light emitting diodes (LEDs) with green and blue light. We envision that this BCNO phosphor will enable the next generation blue and green LED devices due to the easiness of large scale fabrication at an economic cost.

  9. Hydrometallurgical separation of rare earth elements, cobalt and nickel from spent nickel-metal-hydride batteries

    Science.gov (United States)

    Rodrigues, Luiz Eduardo Oliveira Carmo; Mansur, Marcelo Borges

    The separation of rare earth elements, cobalt and nickel from NiMH battery residues is evaluated in this paper. Analysis of the internal content of the NiMH batteries shows that nickel is the main metal present in the residue (around 50% in weight), as well as potassium (2.2-10.9%), cobalt (5.1-5.5%), rare earth elements (15.3-29.0%) and cadmium (2.8%). The presence of cadmium reveals that some Ni-Cd batteries are possibly labeled as NiMH ones. The leaching of nickel and cobalt from the NiMH battery powder with sulfuric acid is efficient; operating variables temperature and concentration of H 2O 2 has no significant effect for the conditions studied. A mixture of rare earth elements is separated by precipitation with NaOH. Finally, solvent extraction with D2EHPA (di-2-ethylhexyl phosphoric acid) followed by Cyanex 272 (bis-2,4,4-trimethylpentyl phosphinic acid) can separate cadmium, cobalt and nickel from the leach liquor. The effect of the main operating variables of both leaching and solvent extraction steps are discussed aiming to maximize metal separation for recycling purposes.

  10. Phosphor blends for high-CRI fluorescent lamps

    Science.gov (United States)

    Setlur, Anant Achyut [Niskayuna, NY; Srivastava, Alok Mani [Niskayuna, NY; Comanzo, Holly Ann [Niskayuna, NY; Manivannan, Venkatesan [Clifton Park, NY; Beers, William Winder [Chesterland, OH; Toth, Katalin [Pomaz, HU; Balazs, Laszlo D [Budapest, HU

    2008-06-24

    A phosphor blend comprises at least two phosphors each selected from one of the groups of phosphors that absorb UV electromagnetic radiation and emit in a region of visible light. The phosphor blend can be applied to a discharge gas radiation source to produce light sources having high color rendering index. A phosphor blend is advantageously includes the phosphor (Tb,Y,LuLa,Gd).sub.x(Al,Ga).sub.yO.sub.12:Ce.sup.3+, wherein x is in the range from about 2.8 to and including 3 and y is in the range from about 4 to and including 5.

  11. Mechanism of extraction of uranium (6) by mixtures of phosphororganic extractants

    International Nuclear Information System (INIS)

    Skorovarov, D.I.; Ul'yanov, V.S.; Meshcheryakov, N.M.; Lagutenkov, V.A.; Mikheev, M.V.

    1988-01-01

    Extraction of uranium (6) from sulfuric acid solutions by solution of D2EHPA-TBP(TOPO) mixture in CCl 4 was studied by NMR method (D2HPA-di-2-ethylhexylphosphoric acid, TBP-tributylphosphate, TOPO-trioctylphosphine oxide). It is shown that stability and stoichiometry of formed solvates depends largely on electron-donor ability of organophosphoric base (TBP or TOPO). The presence of neutral base in extractive system leads to blocking of the coordination center of free D2EHPA molecules, growth of the active acid concentration, assisting in additional solvation of uranyl D2EHP molecules and formation of UO 2 (D2EHP) 2 ·nS type complexes. This results in extraction of additional U(6) quantities to organic phase

  12. White light quality of phosphor converted light-emitting diodes: A phosphor materials perspective of view

    International Nuclear Information System (INIS)

    Sommer, Christian; Hartmann, Paul; Pachler, Peter; Hoschopf, Hans; Wenzl, Franz P.

    2012-01-01

    Highlights: ► We discuss the impact of the optical properties of a phosphor for colour temperature constancy in solid state lighting. ► Quantitative evaluation of permissible variations of the optical properties for batch-to-batch reproducibility. ► Quantitative evaluation of permissible variations of the optical properties upon temperature increase. ► Quantitative evaluation of permissible variations of the optical properties upon materials degradation. - Abstract: For a systematic approach to improve the white light quality of phosphor converted LEDs and to fulfil the demands for colour temperature reproducibility and constancy, it is imperative to understand how variations of the extinction coefficient and the quantum efficiency of the phosphor particles as well as variations of the excitation wavelength of the blue LED die affect the correlated colour temperature of the white LED source. Based on optical ray tracing of a phosphor converted white LED package we deduce permissible values for the variation of a given extinction coefficient and a given quantum efficiency of a phosphor material in order to maintain acceptable colour variations. These quantitative valuations of the required constancy of the optical properties of the phosphors will in particular provide some benchmarks for the synthesis of improved phosphor materials aiming at solid state lighting applications.

  13. The use of a polymer inclusion membrane in a paper-based sensor for the selective determination of Cu(II).

    Science.gov (United States)

    Jayawardane, B Manori; Coo, Lilibeth dlC; Cattrall, Robert W; Kolev, Spas D

    2013-11-25

    A disposable paper-based sensor (PBS) is described for the determination of Cu(II) in natural and waste waters at approximately 2 cents per measurement. The device makes use of a polymer inclusion membrane (PIM) to provide the selectivity for Cu(II). The PIM consists of 40 wt% di(2-ethlyhexyl) phosphoric acid (D2EHPA) as the carrier, 10 wt% dioctyl phthalate (DOP) as a plasticizer, 49.5 wt% poly(vinyl chloride) (PVC) as the base polymer and 0.5 wt% (mm(-1)) 1-(2'-pyridylazo)-2-naphthol (PAN) as the colourimetric reagent. High selectivity under mildly acidic conditions (HCl, pH 2.0) is achieved for Cu(II) in the presence of frequently encountered metal ions in natural and waste waters such as Fe(III), Al(III), Zn(II), Cd(II), Pb(II), Ca(II), Mg(II), and Ni(II). The laminated PBS consists of a PIM sensing disc (2mm in diameter) attached to the centre of a circular hydrophilic zone (7 mm in diameter) pretreated with 0.01 M HCl. This hydrophilic zone separates the sample port (a circular hole in the plastic cover) from the PIM sensing disc. After introducing 19.2 μL of a sample/standard solution to the sample port, Cu(II) diffuses across the hydrophilic zone and is extracted into the PIM disc as the Cu(II)-D2EHPA complex which subsequently reacts with PAN to produce the red-purple coloured Cu(II)-PAN complex. The colour intensity of the PIM disc is measured 15 min after sample/standard introduction by scanning using a flatbed scanner. Under optimal conditions the device is characterized by a limit of detection (LOD) and limit of quantitation (LOQ) of 0.06 and 0.21 mg L(-1) Cu(II), respectively, with two linear ranges together covering the Cu(II) concentration range from 0.1 to 30.0 mg L(-1). The PBS was successfully applied to the determination of Cu(II) in hot tap water and mine tailings water. Copyright © 2013 Elsevier B.V. All rights reserved.

  14. Extraction of Tetravalent Uranium by Certain Acidic Organophosphorus Extractants from Phosphate Medium

    International Nuclear Information System (INIS)

    Daoud, J.A.; Zeid, M.M.; Aly, H.F.

    1998-01-01

    The extraction of U(IV) by octylphenyl acid phosphate (OPAP) or di-2-ethylhexyl phosphoric acid (HDEHP) in kerosene from phosphoric acid was carried out. The effect of extractant, phosphoric acid, uranium, Fe(II) and Fe(III) concentration on the extraction process was separately investigated. The effect of different reagents and temperature on the stripping of U(IV) was also investigated. The results obtained for the extraction of U(IV) by HDEHP showed that the extraction with the increase in HDEHP and Fe(III) concentration while it decreases with the increase in phosphoric acid, uranium and Fe(II) concentration. In case of extraction with OPAP, the extraction of U(IV) was found to decrease with the phosphoric acid, Fe(II) and initial uranium concentration while the increase in OPAP concentration slightly affected the extraction. The use of high phosphoric acid concentration as stripper at low temperature was found to give the best stripping results

  15. High efficiency nitride based phosphores for white LEDs

    NARCIS (Netherlands)

    Li, Yuan Qiang; Hintzen, H.T.J.M.

    2008-01-01

    In this overview paper, novel rare-earth doped silicon nitride based phosphors for white LEDs applications have been demonstrated. The luminescence properties of orange-red-emitting phosphors (M2Si5N8:Eu2+) and green-to-yellow emitting phosphors (MSi2N2O2:Eu2+, M = Ca, Sr, Ba) are discussed in

  16. Optical property investigations of polystyrene capped Ca2P2O7:Dy3+ persistent phosphor

    International Nuclear Information System (INIS)

    Jain, Abhilasha; Kumar, Ashwini; Dhoble, S.J; Peshwe, D.R

    2015-01-01

    Highlights: • Synthesis of polymer capped pyrophosphate phosphors by citrate gel method. • Radiative lifetime is calculated from parameters of Judd-Ofelt theory and ICP-AES. • Reaction mechanism is discussed leading to high photoluminescence efficiency. • PL emission spectrum reveals broad band emission suitable for solid state lighting. - Abstract: By virtue of enhanced photosensivity, good optical response and better thermal stability, organic–inorganic hybrid materials are contemplated as one of the alternatives for designing advanced optoelectronic devices and innovative photonic applications. A novel inorganic organic hybrid Ca 2 P 2 O 7 :Dy 3+ phosphor has been fabricated by Pechini method. The optical property of synthesized phosphor is successfully altered by the in corporation of polystyrene sulfonic acid as capping agent in the colloidal solution. The phase purity and the average particle size of the prepared phosphor were calculated from X-ray diffraction (XRD) employing Debye Scherrer method. The morphological and chemical investigations were carried out through scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) analysis. The radiative transitions are explained on the basis of Judd-Ofelt theory and on the basis of derived parameters, the radiative lifetime of persistent hybrid Ca 2 P 2 O 7 :Dy 3+ phosphor is calculated as 5.33 ms. This paper explores the mechanism leading to high photoluminescence efficiency using organic capping additives. The photoluminescence (PL) graphs reveal broad band emission at 482 nm (blue) and 573 nm (yellow) corresponding to 4 F 9/2 - 6 H 15/2 and 4 F 9/2 - 6 H 13/2 transitions of Dy 3+ , respectively. The Commission International De I-Eclairage (CIE) chromaticity co-ordinates were calculated from emission spectra and the values (x, y) were approaching to standard value of white emission. The synthesized pyrophosphate phosphors can thereby account in multiple potential applications

  17. Design of Biochemical Oxidation Process Engineering Unit for Treatment of Organic Radioactive Liquid Waste

    International Nuclear Information System (INIS)

    Zainus Salimin; Endang Nuraeni; Mirawaty; Tarigan, Cerdas

    2010-01-01

    Organic radioactive liquid waste from nuclear industry consist of detergent waste from nuclear laundry, 30% TBP-kerosene solvent waste from purification or recovery of uranium from process failure of nuclear fuel fabrication, and solvent waste containing D 2 EHPA, TOPO, and kerosene from purification of phosphoric acid. The waste is dangerous and toxic matter having low pH, high COD and BOD, and also low radioactivity. Biochemical oxidation process is the effective method for detoxification of organic waste and decontamination of radionuclide by bio sorption. The result process are sludges and non radioactive supernatant. The existing treatment facilities radioactive waste in Serpong can not use for treatment of that’s organics waste. Dio chemical oxidation process engineering unit for continuous treatment of organic radioactive liquid waste on the capacity of 1.6 L/h has been designed and constructed the equipment of process unit consist of storage tank of 100 L capacity for nutrition solution, 2 storage tanks of 100 L capacity per each for liquid waste, reactor oxidation of 120 L, settling tank of 50 L capacity storage tank of 55 L capacity for sludge, storage tank of 50 capacity for supernatant. Solution on the reactor R-01 are added by bacteria, nutrition and aeration using two difference aerators until biochemical oxidation occurs. The sludge from reactor of R-01 are recirculated to the settling tank of R-02 and on the its reverse operation biological sludge will be settled, and supernatant will be overflow. (author)

  18. A survey of phosphors novel for thermography

    Energy Technology Data Exchange (ETDEWEB)

    Bruebach, J., E-mail: bruebach@ekt.tu-darmstadt.d [Fachgebiet Reaktive Stroemungen und Messtechnik, Center of Smart Interfaces Technische Universitaet Darmstadt, Petersenstrasse 32, 64287 Darmstadt (Germany); Kissel, T. [Fachgebiet Reaktive Stroemungen und Messtechnik, Center of Smart Interfaces Technische Universitaet Darmstadt, Petersenstrasse 32, 64287 Darmstadt (Germany); Frotscher, M. [Eduard-Zintl-Institut fuer Anorganische und Physikalische Chemie, Technische Universitaet Darmstadt, Petersenstrasse 18, 64287 Darmstadt (Germany); Euler, M. [Fachgebiet Reaktive Stroemungen und Messtechnik, Center of Smart Interfaces Technische Universitaet Darmstadt, Petersenstrasse 32, 64287 Darmstadt (Germany); Albert, B. [Eduard-Zintl-Institut fuer Anorganische und Physikalische Chemie, Technische Universitaet Darmstadt, Petersenstrasse 18, 64287 Darmstadt (Germany); Dreizler, A. [Fachgebiet Reaktive Stroemungen und Messtechnik, Center of Smart Interfaces Technische Universitaet Darmstadt, Petersenstrasse 32, 64287 Darmstadt (Germany)

    2011-04-15

    With regard to phosphor thermometry, seven luminescent ceramic materials were synthesised and characterised, namely CaMoO{sub 4}:Eu{sup 3+}, CaTiO{sub 3}:Pr{sup 3+}, LaPO{sub 4}:Eu{sup 3+}, LaVO{sub 4}:Eu{sup 3+}, LiAl{sub 5}O{sub 8}:Fe{sup 3+}, TiMg{sub 2}O{sub 4}:Mn{sup 4+} and ZnGa{sub 2}O{sub 4}:Mn{sup 2+}. In this context, emission spectra and temperature lifetime characteristics are presented. Thus, a survey of phosphors novel for thermography is given in order to encourage further studies and more detailed characterisations of the respective materials. - Research Highlights: Seven phosphor materials novel for thermometry were synthesised. These materials were characterised diffractometrically as well as concerning their emission spectra and lifetime temperature characteristics. The number of phosphor materials characterised for thermometry purposes was extended by seven materials.

  19. Phosphate phosphors for solid-state lighting

    Energy Technology Data Exchange (ETDEWEB)

    Shinde, Kartik N. [N.S. Science and Arts College, Bhadrawati (India). Dept. of Physics; Swart, H.C. [University of the Orange Free State, Bloemfontein (South Africa). Dept. of Physics; Dhoble, S.J. [R.T.M. Nagpur Univ. (India). Dept. of Physics; Park, Kyeongsoon [Sejong Univ., Seoul (Korea, Republic of). Faculty of Nanotechnology and Advanced Materials Engineering

    2012-07-01

    Essential information for students in researchers working towards new and more efficient solid-state lighting. Comprehensive survey based on the authors' long experience. Useful both for teaching and reference. The idea for this book arose out of the realization that, although excellent surveys and a phosphor handbook are available, there is no single source covering the area of phosphate based phosphors especially for lamp industry. Moreover, as this field gets only limited attention in most general books on luminescence, there is a clear need for a book in which attention is specifically directed toward this rapidly growing field of solid state lighting and its many applications. This book is aimed at providing a sound introduction to the synthesis and optical characterization of phosphate phosphor for undergraduate and graduate students as well as teachers and researchers. The book provides guidance through the multidisciplinary field of solid state lighting specially phosphate phosphors for beginners, scientists and engineers from universities, research organizations, and especially industry. In order to make it useful for a wide audience, both fundamentals and applications are discussed, together.

  20. doped LiMgPO4 phosphor

    Indian Academy of Sciences (India)

    attention because of their remarkable luminescence proper- ties and .... Figure 1. (a) X-ray diffraction patterns of LiMgPO4:Tb3+ phosphor and (b) standard data. ICDD file. .... ground signal which affects the signal to noise ratio [17]. MDD was ...