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...

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...

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...

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...

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.)

Effect of annealing on structural and luminescence properties of Eu3+ doped NaYF4 phosphor

Science.gov (United States)

Pathak, Trilok K.; Kumar, Ashwini; Swart, H. C.; Kroon, R. E.

2018-04-01

Eu3+ doped NaYF4 phosphors have been synthesized by the combustion method. The effect of annealing on the structural, morphological and luminescence properties has been investigated. X-ray diffraction analysis revealed that the Eu3+ doped NaYF4 phosphors consisted of mixed phases: α-phase and β-phase which were affected by the annealing of the phosphor. The surface morphology showed a significant change with annealing in the Eu3+ doped NaYF4 phosphors. The elemental mapping and energy dispersive X-ray spectroscopy spectra proved the formation of the desired materials. The photoluminescence spectra illustrated the optical properties of Eu3+ in the as-prepared and annealed Eu3+ doped NaYF4 phosphors. The intensity of the peaks 5D0 → 7F2 and 5D0 → 7F1 varied in as-prepared and annealed samples. The lifetime of the Eu3+ luminescence at 615 nm was also weakly affected by the Eu3+ doping and annealing temperature.

Thermoluminescence dosimetric characteristics of thulium doped ZnB{sub 2}O{sub 4} phosphor

Energy Technology Data Exchange (ETDEWEB)

Annalakshmi, O. [Radiological Safety Division, Indira Gandhi Centre for Atomic Research, Kalpakkam-603102 (India); Jose, M.T., E-mail: mtj@igcar.gov.in [Radiological Safety Division, Indira Gandhi Centre for Atomic Research, Kalpakkam-603102 (India); Madhusoodanan, U. [Radiological Safety Division, Indira Gandhi Centre for Atomic Research, Kalpakkam-603102 (India); Subramanian, J. [Central Leather Research Institute, Council of Scientific and Industrial Research, Chennai (India); Venkatraman, B. [Radiological Safety Division, Indira Gandhi Centre for Atomic Research, Kalpakkam-603102 (India); Amarendra, G. [Materials Physics Division, Indira Gandhi Centre for Atomic Research, Kalpakkam-603102 (India); Mandal, A.B. [Central Leather Research Institute, Council of Scientific and Industrial Research, Chennai (India)

2014-02-15

Polycrystalline powder samples of rare earth doped Zinc borates were synthesized by high temperature solid state diffusion technique. Dosimetric characteristics of the phosphor like thermoluminescence glow curve, TL emission spectra, dose–response, fading studies, reproducibility and reusability studies were carried out on the synthesized phosphors. Among the different rare earth doped phosphors, thulium doped zinc borate was found to have a higher sensitivity. Hence detailed dosimetric characteristics of this phosphor were carried out. It is observed that the dose–response is linear from 10 mGy to 10{sup 3} Gy in this phosphor. EPR measurements were carried out on unirradiated, gamma irradiated and annealed phosphors to identify the defect centers responsible for thermoluminescence. A TL model is proposed based on the EPR studies in these materials. Kinetic parameters were evaluated for the dosimetric peaks using various methods. The experimental results show that this phosphor can have potential applications in radiation dosimetry applications. -- Highlights: • Polycrystalline powder samples of rare earth doped zinc borates were synthesized. • Thulium was observed to be the most efficient dopant in ZnB{sub 2}O{sub 4} lattice. • TL intensity of the dosimetric peak is around 20 times that of TLD-100. • Based on EPR studies a TL mechanism is proposed in zinc borate. • Deconvolution of the glow curve carried out.

Emission spectra of phosphor MgSO4 doped with Dy and Mn

International Nuclear Information System (INIS)

Zhang Chunxiang; Chen Lixin; Tang Qiang; Luo Daling; Qiu Zhiren

2001-01-01

Emission spectra of phosphor MgSO 4 doped with Dy and Dy/Mn were measured with an optical multichannel analyzer and a linear heating system whose temperature was controlled by a microcomputer. The emission spectrum bands at 480 nm and 580 nm of phosphor MgSO 4 doped with Dy were observed in the three dimensional (3D) glow curves. Compared with the 3D spectrum of CaSO 4 :Dy and the spectrum bands of MgSO 4 :Dy shows the same wavelengths which resulted from the quantum transitions among the energy levels of Dy 3 '+ ions. The intensities of the glow peaks in both spectrum bands (480 nm and 580 nm) of phosphor MgSO 4 doped with Dy/Mn were dramatically reduced except the 380 degree C glow peak

Photoluminescence properties of Li{sup +}-doped KNbO{sub 3}: Eu{sup 3+} phosphors

Energy Technology Data Exchange (ETDEWEB)

Balakrishnaiah, R.; Kim, Dongwoo; Yi, Soungsoo; Kim, Sunghoon [Silla University, Busan (Korea, Republic of); Jang, Kiwan; Lee, Hosueb [Changwon National University, Changwon (Korea, Republic of); Moon, Byungkee; Jeong, Junghyun [Pukyong National University, Busan (Korea, Republic of)

2010-12-15

Different concentrations of Li{sup +}-ions doped KNbO{sub 3}:Eu polycrystalline powder phosphors were prepared by using the conventional solid state reaction method and were characterized by using X-ray diffraction, field emission scanning electron microscopy, and by using photoluminescence excitation and emission measurements. The morphological and the photoluminescence properties of the phosphors were effectively improved with Li-doping. The PL properties as a function of Li concentration in the Li-doped KNbO{sub 3}:Eu phosphors using different excitation wavelengths, along with a comparison of results with these in similar reported works, are discussed in the present work.

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)

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.

Effect of Er doping on optical transmission and EL spectra of (Zn, Cd)S:Cu phosphors

International Nuclear Information System (INIS)

Patil, P.K.; Nandgave, J.K.; Lawangar Pawar, R.D.

1991-01-01

Powder phosphors((Znsub(0.4)Cdsub(0.6))S)doped with Cu and Er have been prepared under the inert atmosphere of argon. The optical transmission spectra of Cu doped phosphors have been investigated and explained on the basis of copper associated defect states. The improvement of optical transmission of the phosphors due to Er doping has been reported and explained. The EL emission spectrum of (Znsub(0.4)Cdsub(0.6))S:Cu:Er phosphors exhibits two broad bands characteristic of Cu. The absence of characteristic Er bands has been explained as an effect of thermal quenching of Er donor levels. (author). 9 refs., 2 figs

Co-doping with antimony to control phosphorous diffusion in germanium

KAUST Repository

Tahini, H. A.

2013-02-15

In germanium, phosphorous and antimony diffuse quickly and as such their transport must be controlled in order to design efficient n-typed doped regions. Here, density functional theory based calculations are used to predict the influence of double donor co-doping on the migration activation energies of vacancy-mediated diffusion processes. The migration energy barriers for phosphorous and antimony were found to be increased significantly when larger clusters involving two donor atoms and a vacancy were formed. These clusters are energetically stable and can lead to the formation of even larger clusters involving a number of donor atoms around a vacancy, thereby affecting the properties of devices.

Synthesis and luminescence properties of Eu"2"+ doped CaSO_4 phosphor

International Nuclear Information System (INIS)

Aghalte, G.A.; Dhoble, S.J.; Pawar, N.R.

2016-01-01

Eu"2"+ doped CaSO_4 Phosphor were synthesized by precipitation method. PL analysis of Eu"2"+ activated CaSO_4 phosphor exhibited characteristic emission properties; CaSO_4:Eu Phosphor has received considerable attention because of its high sensitivity to X-ray and λ ray irradiation. CaSO_4:Eu phosphor powder was successfully synthesized by the wet chemical co-precipitation method. The structure morphology and luminescent properties of the phosphor were characterized by X-ray diffraction, scanning electron microscopy and photoluminescence spectroscopy

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

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.

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....

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

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...

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

Study of effect of co-doping on CIE coordinates of strontium cerium oxide phosphor (Sr_2CeO_4)

International Nuclear Information System (INIS)

Zambare, Pradip Z.; Ahirrao, P.B.; Chaudhari, D.B.; Zambare, A.P.; Mahajan, O.H.

2016-01-01

The phosphors Sr_2CeO_4 doped europium and gadolinium were synthesized by modified solid state diffusion method. From emission spectra, the CIE coordinates (x, y) of x% Eu"3"+ and 0.5 %Gd"3"+ doped Sr_2CeO_4 phosphors was calculated. In present paper, we investigate luminescence properties and colorimetric study of Sr_2CeO_4 doped 0.5% Gd"3"+, x% Eu"3"+. The phosphors Sr_2CeO_4 doped europium and gadolinium were successfully synthesized by modified solid state diffusion method. X-ray diffraction (XRD) profile confirms the orthorhombic nature of Eu"3"+ and 0.5% Gd"3"+ doped Sr_2CeO_4 phosphors. In addition, scanning electron Microscopy (SEM), Fourier-Transformation IR spectroscopy (FTIR), was also used to study the synthesized phosphors

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)

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)

Spectral properties of Dy3+ doped ZnAl2O4 phosphor

Science.gov (United States)

Prakash, Ram; Kumar, Sandeep; Mahajan, Rubby; Khajuria, Pooja; Kumar, Vinay; Choudhary, R. J.; Phase, D. M.

2018-05-01

Herein, Dy3+ doped ZnAl2O4 phosphor was synthesized by the solution combustion method. The synthesized phosphor was characterized by X-ray diffraction (XRD), photoluminescence (PL) spectroscopy, UV-Vis spectroscopy and X-ray photoelectron spectroscopy (XPS). The phase purity of the phosphor was confirmed by the XRD studies that showed cubic symmetry of the synthesized phosphor. Under UV excitation (388 nm) the PL emission spectrum of the phosphor shows characteristic transition from the Dy3+ ion. A band gap of 5.2 eV was estimated from the diffused reflectance spectroscopy. The surface properties of the phosphor were studied using the X-ray photoelectron spectroscopy.

Lanthanide-doped upconverting phosphors for bioassay and therapy

Science.gov (United States)

Guo, Huichen; Sun, Shiqi

2012-10-01

Lanthanide-doped fluorescent materials have gained increasing attention in recent years due to their unique luminescence properties which have led to their use in wide-ranging fields including those of biological applications. Aside from being used as agents for in vivo imaging, lanthanide-doped fluorescent materials also present many advantages for use in bioassays and therapy. In this review, we summarize the applications of lanthanide-doped up-converting phosphors (UCPs) in protein and gene detection, as well as in photodynamic and gene therapy in recent years, and outline their future potential in biological applications. The current report could serve as a reference for researchers in relevant fields.

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

Photovoltaic Performance Characterization of Textured Silicon Solar Cells Using Luminescent Down-Shifting Eu-Doped Phosphor Particles of Various Dimensions.

Science.gov (United States)

Ho, Wen-Jeng; Deng, Yu-Jie; Liu, Jheng-Jie; Feng, Sheng-Kai; Lin, Jian-Cheng

2017-01-01

This paper reports on efforts to enhance the photovoltaic performance of textured silicon solar cells through the application of a layer of Eu-doped silicate phosphor with particles of various dimensions using the spin-on film technique. We examined the surface profile and dimensions of the Eu-doped phosphors in the silicate layer using optical microscopy with J-image software. Optical reflectance, photoluminescence, and external quantum efficiency were used to characterize the luminescent downshifting (LDS) and light scattering of the Eu-doped silicate phosphor layer. Current density-voltage curves under AM 1.5G simulation were used to confirm the contribution of LDS and light scattering produced by phosphor particles of various dimensions. Experiment results reveal that smaller phosphor particles have a more pronounced effect on LDS and a slight shading of incident light. The application of small Eu-doped phosphor particles increased the conversion efficiency by 9.2% (from 12.56% to 13.86%), far exceeding the 5.6% improvement (from 12.54% to 13.32%) achieved by applying a 250 nm layer of SiO₂ and the 4.5% improvement (from 12.37% to 12.98%) observed in cells with large Eu-doped phosphor particles.

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

Development and characterization of acid-doped polybenzimidazole/sulfonated polysulfone blend polymer electrolytes for fuel cells

DEFF Research Database (Denmark)

Hasiotis, C.; Li, Qingfeng; Deimede, V.

2001-01-01

Polymeric membranes from blends of sulfonated polysulfones (SPSF) and polybenzimidazole (PBI) doped with phosphoric acid were developed as potential high-temperature polymer electrolytes for fuel cells and other electrochemical applications. The water uptake and acid doping of these polymeric...... membranes were investigated. Ionic conductivity of the membranes was measured in relation to temperature, acid doping level, sulfonation degree of SPSF, relative humidity, and blend composition. The conductivity of SPSF was of the order of 10/sup -3/ S cm/sup -1/. In the case of blends of PBI and SPSF...

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

Structure, electronic properties, luminescence and chromaticity investigations of rare earth doped KMgBO{sub 3} phosphors

Energy Technology Data Exchange (ETDEWEB)

Zheng, Jianghui; Cheng, Qijin [School of Energy Research, Xiamen University, Xiamen 361005 (China); Wu, Shunqing [Department of Physics, Xiamen University, Xiamen, 361005 (China); Zhuang, Yixi [College of Materials, Xiamen University, Xiamen 361005 (China); Guo, Ziquan; Lu, Yijun [Department of Electronic Science, Fujian Engineering Research Center for Solid-state Lighting, Xiamen University, Xiamen 361005 (China); Chen, Chao, E-mail: cchen@xmu.edu.cn [School of Energy Research, Xiamen University, Xiamen 361005 (China); Department of Physics, Xiamen University, Xiamen, 361005 (China); Department of Electronic Science, Fujian Engineering Research Center for Solid-state Lighting, Xiamen University, Xiamen 361005 (China)

2015-09-01

In this work, the optimization of the geometry and the electronic properties of the host matrix KMgBO{sub 3} were investigated using density functional theory, and the comprehensive photoluminescence and chromaticity properties on five rare earth ion-doped (RE = Ce{sup 3+}, Tm{sup 3+}, Tb{sup 3+}, Eu{sup 3+}, Dy{sup 3+}) KMgBO{sub 3} phosphors were also studied. By introducing RE ions into the KMgBO{sub 3} host, excellent purple, blue, green, red and white emitting light could be obtained under the near-ultraviolet light excitation. The results suggest that rare earth doped KMgBO{sub 3} phosphors are potential luminescence materials for the application in the near-ultraviolet white light-emitting diodes. - Highlights: • The electronic properties of the host matrix KMgBO{sub 3} were investigated. • The PL properties on rare earth ions doped KMgBO{sub 3} phosphors were studied. • The chromaticity properties on rare earth ions doped KMgBO{sub 3} samples were studied. • Tm{sup 3+} and Eu{sup 3+} doped KMgBO{sub 3} samples show higher color purity than commercial phosphors.

Enhanced red emission of LaVO4:Eu3+ phosphors by Li-doping

International Nuclear Information System (INIS)

Park, Sung Wook; Yang, Hyun Kyoung; Chung, Jong Won; Moon, Byung Kee; Choi, Byung Chun; Jeong, Jung Hyun; Jang, Ki Wan; Lee, Ho Sueb; Yi, Soung Soo

2010-01-01

LaVO 4 phosphors were synthesized by using a solid state reaction, and were characterized by using X-ray diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence (PL). The XRD patterns of the Li-doped LaVO 4 :Eu 3+ powder phosphors revealed a mixture of tetragonal and monoclinic phases. The tetragonal phase of the LaVO 4 :Eu 3+ phosphor showed a higher PL intensity than the monoclinic one, despite the presence of both monoclinic and tetragonal structures. The Li-doped LaVO 4 :Eu 3+ powder phosphors absorbed strongly at 396 nm and exhibited strong red emission at approximately 619.5 nm due to the 5 D 0 → 7 F 2 transition. The incorporation of Li + ions into the LaVO 4 :Eu 3+ powder can lead to a remarkable increase in photoluminescence. The enhanced luminescence is attributed to the incorporation of Li + ions that may act as a sensitizers for effective energy transfer. This phosphor has promising applications in near-UV light-emitting diodes(LEDs).

TL characterization of Ag co-doped SrSO{sub 4}:Eu phosphor for gamma dosimetry applications

Energy Technology Data Exchange (ETDEWEB)

Jayasudha, S., E-mail: jsnair.india@gmail.com [Mahatma Gandhi College, Pattom Palace P.O., Thiruvananthapuram 695004 (India); Madhukumar, K.; Nair, C.M.K.; Nair, Resmi G.; Anandakumar, V.M. [Mahatma Gandhi College, Pattom Palace P.O., Thiruvananthapuram 695004 (India); Elias, T.S. [State Institute of Cancer Research, Medical College P.O., Thiruvananthapuram 695011 (India); Rajesh, S. [Campus Universitario de Santiago, Aveiro (Portugal)

2017-04-15

High temperature thermoluminescence (TL) emissions and improvement in fading due to the co-doping ofr Ag in the SrSO{sub 4}:Eu phosphor synthesized through chemical precipitation technique when subjected to γ-excitation is discussed. The dopant concentrations were tuned for optimum TL sensitivity. Preliminary crystallographic and structural studies of the phosphors were done using PXRD, SEM, and TEM. The phosphor has a single phase orthorhombic lattice structure and the crystallites are found to be nanostructured. The presence of dopants in the host matrix is established through EDS and ICP-AES studies. The TL glow curve shows a single intense emission at 314 ├ó┬ü┬░C under γ- exposure of dose 1 Gy, which is given from a {sup 60}Co build-up. The dosimetric properties such as sensitivity, dose dependence, fading and reusability of SrSO{sub 4}:Eu,Ag phosphor were also studied. It is observed that co-doping with Ag improves the fading rate of the SrSO{sub 4}:Eu phosphor by about 5%. Even though the luminescence intensity is found to be less than that of SrSO{sub 4}:Eu phosphor, the Ag co-doped phosphor becomes significant owing to its improved fading rate and high temperature afterglow. The gamma sensitivity of the SrSO{sub 4}:Eu,Ag(0.5,0.5 mol%) phosphor is compared to that of the standard CaSO{sub 4}:Dy TLD phosphor. The TL kinetic parameters were calculated using IR, Chen's peak shape method and verified by the theoretical fit using GCD functions. - Highlights: • A High temperature TL emission is observed for the SrSO{sub 4}:Eu,Ag phosphor. • TL intensity is 10 times higher than that of standard CaSO{sub 4}:Dy. • Fading rate of SrSO{sub 4}:Eu phosphor is improved by 5% with Ag co-doping. • Linear dose response in the range 10mGy-10Gy. • t .

NIR to visible upconversion in Er3+/Yb3+ co-doped CaYAl3O7 phosphor obtained by solution combustion process

International Nuclear Information System (INIS)

Singh, Vijay; Rai, Vineet Kumar; Al-Shamery, Katharina; Nordmann, Joerg; Haase, Markus

2011-01-01

Using the combustion synthesis, CaYAl 3 O 7 :Er 3+ phosphor powders co-doped with Yb 3+ have been prepared at low temperatures (550 o C) in a few minutes. Formation of the compound was confirmed by X-ray powder diffraction. Near-infrared to visible upconversion fluorescence emission in the Er 3+ doped CaYAl 3 O 7 phosphor powder has been observed. The effect of co-doping with triply ionized ytterbium in the CaYAl 3 O 7 :Er 3+ phosphor has been studied and the process involved is discussed. - Highlights: → The green emitting up-conversion CaYAl 3 O 7 :Er 3+ phosphor powders co-doped with Yb 3+ have been prepared by easy combustion method. → The combustion method is a simple, energy saving, fast and economical viable process. → The luminescence intensity in the co-doped phosphor is enhanced by several times compared to that of the singly (Er 3+ ) doped phosphor.

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)

Energy transfer and colorimetric properties of Eu3+/Dy3+ co-doped Gd2(MoO4)3 phosphors

International Nuclear Information System (INIS)

Wan Jing; Cheng Lihong; Sun Jiashi; Zhong Haiyang; Li Xiangping; Lu Weili; Tian Yue; Lin Hai; Chen Baojiu

2010-01-01

Dy 3+ single-doped and Eu 3+ /Dy 3+ co-doped gadolinium molybdate (Gd 2 (MoO 4 ) 3 ) phosphors were synthesized by a traditional solid-state reaction method. The XRD was used to confirm the crystal structure of the phosphors. The energy transfer between Eu 3+ and Dy 3+ was observed and studied. The Eu 3+ concentration can hardly affect the blue and yellow emission intensities of Dy 3+ , and the Eu 3+ emission intensity increases with the increase of Eu 3+ concentration. Co-doping with Eu 3+ compensated the red emission component of the Dy 3+ doped Gd 2 (MoO 4 ) 3 phosphor. Introducing proper amount of Eu 3+ can improve the colorimetric performance of the phosphors.

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%...

Co-doping with antimony to control phosphorous diffusion in germanium

KAUST Repository

Tahini, H. A.; Chroneos, Alexander; Grimes, R. W.; Schwingenschlö gl, Udo

2013-01-01

donor co-doping on the migration activation energies of vacancy-mediated diffusion processes. The migration energy barriers for phosphorous and antimony were found to be increased significantly when larger clusters involving two donor atoms and a vacancy

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...

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.)

UV, blue and red upconversion emission in Tm3+ doped Y2O3 phosphor

International Nuclear Information System (INIS)

Pandey, Anurag; Kaushal Kumar; Rai, Vineet Kumar

2012-01-01

Optimized solution combustion route has been adopted to prepare Tm 3+ doped Y 2 O 3 phosphor. The X-ray diffraction analysis of the doped phosphor for getting the structural information has been performed. Intense UV, blue and red emissions exhibiting narrow band have been monitored using 980 nm diode laser excitation. The origin of UV, blue and red upconversion emissions has been explained based on the available data. (author)

Radiation-induced defects in manganese-doped lithium tetraborate phosphor.

Science.gov (United States)

Annalakshmi, O; Jose, M T; Madhusoodanan, U; Sridevi, J; Venkatraman, B; Amarendra, G; Mandal, A B

2015-01-01

Lithium tetraborate doped with manganese synthesised by solid-state sintering technique exhibits a dosimetric peak at 280°C. The high-temperature glow curve results in no fading for three months. The sensitivity of Li2B4O7:Mn is determined to be 0.9 times that of TLD-100. The infrared spectrum of this phosphor indicates the presence of bond vibrations corresponding to BO4 tetrahedral and BO3 triangles. The mechanism for thermoluminescence in this phosphor was proposed based on the thermoluminescence (TL) emission spectra, kinetic analysis of TL glow curves and electron paramagnetic resonance (EPR) measurements on non-irradiated and gamma-irradiated phosphors. It was identified that oxygen vacancies and Boron oxygen hole centre (BOHC) are the electron and hole trap centres for TL in this phosphor. When the phosphor is heated, the electrons are released from the electron trap and recombine with the trapped holes. The excitation energy during the recombination is transferred to the nearby Mn(2+) ions, which emit light at 580 nm. © The Author 2014. Published by Oxford University Press. All rights reserved. For Permissions, please email: journals.permissions@oup.com.

Long afterglow property of Er"3"+ doped Ca_2SnO_4 phosphor

International Nuclear Information System (INIS)

Zhang, Dongyun; Shi, Mingming; Sun, Yiwen; Guo, Yunyun; Chang, Chengkang

2016-01-01

A novel green emitting long afterglow phosphor, Er"3"+ -doped Ca_2SnO_4 (Ca_2SnO_4:Er"3"+), was prepared successfully via a traditional high temperature solid–state reaction method. Its properties have been characterized and analyzed by utilizing x-ray diffraction (XRD), photoluminescence spectroscope (PLS), afterglow decay curve (ADC) and thermal luminescence spectroscope (TLS). Three main emission peaks of PLS locate at 524, 550 and 668 nm, corresponding to CIE chromaticity coordinates of x = 0.326, y = 0.6592. An optimal doping concentration of Er"3"+ of 2% was determined. The Ca_2SnO_4:Er"3"+ phosphors showed a typical triple-exponential afterglow decay behavior when the UV source was switched off. Thermal simulated luminescence study indicated that the persistent afterglow of Ca_2SnO_4:2 mol% Er"3"+ phosphors was generated by the suitable electron or hole traps which were resulted from the doping the Ca_2SnO_4 host with rare-earth ions (Er"3"+). - Highlights: • A novel green emitting long afterglow phosphor, Ca_2SnO_4:Er"3"+, was prepared. • An optimal doping concentration of Er"3"+ of 2% was determined. • After the UV source was turned off, the Ca_2SnO_4:Er"3"+ showed a typical triple-exponential afterglow decay behavior. • CIE chromaticity coordinates results confirmed a green light emitting of the Ca_2SnO_4:Er"3"+. • The persistent afterglow of the Ca_2SnO_4:Er"3"+ was attributed to suitable electron or hole traps.

TL process in europium doped alkaline earth sulphate phosphors- a review

International Nuclear Information System (INIS)

Bhatt, B.C.

2003-01-01

CaSO 4 doped with the rare earth (RE) ion dysprosium or thulium is used routinely as a thermoluminescent dosimeter (TLD) to monitor personal exposure to x- and γ-radiation. The CaSO 4 :Eu phosphor is potentially important for radio photoluminescence (RPL) and ultraviolet (UV) dosimetry. Eu 3+ → Eu 2+ conversion is suggested to play a pivotal role in UV and γ-ray induced thermoluminescence. However, there is disagreement among different workers on the mechanism of gamma and UV induced TL in this phosphor system. This paper will review the work reported on CaSO 4 :Eu and make effects to project overall picture on this phosphor system. (author)

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.

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.)

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)

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

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.

Rare Earth Doped Lanthanum Calcium Borate Polycrystalline Red Phosphors

Directory of Open Access Journals (Sweden)

H. H. Xiong

2014-01-01

Full Text Available Single-phased Sm3+ doped lanthanum calcium borate (SmxLa2−xCaB10O19, SLCB, x=0.06 polycrystalline red phosphor was prepared by solid-state reaction method. The phosphor has two main excitation peaks located at 398.5 nm and 469.0 nm, which are nicely in accordance with the emitting wavelengths of commercial near-UV and blue light emitting diode chips. Under the excitation of 398.0 nm, the dominant red emission of Sm3+ in SLCB phosphor is centered at 598.0 nm corresponding to the transition of 4G5/2 → 6H7/2. The Eu3+ fluorescence in the red spectral region is applied as a spectroscopic probe to reveal the local site symmetry in the host lattice and, hence, Judd-Ofelt parameters Ωt  (t=2, 4 of Eu3+ in the phosphor matrix are derived to be 3.62×10-20 and 1.97×10-20 cm2, indicating a high asymmetrical and strong covalent environment around rare earth luminescence centers. Herein, the red phosphors are promising good candidates employed in white light emitting diodes (LEDs illumination.

Color tunable emission through energy transfer from Yb3+ co-doped SrSnO3: Ho3+ perovskite nano-phosphor

Science.gov (United States)

Jain, Neha; Singh, Rajan Kr.; Sinha, Shriya; Singh, R. A.; Singh, Jai

2018-04-01

First time color tunable lighting observed from Ho3+ and Yb3+ co-doped SrSnO3 perovskite. Down-conversion and up-conversion (UC) photoluminescence emission spectra were recorded to understand the whole mechanism of energy migration between Ho3+ and Yb3+ ions. The intensity of green and red emission varies with Yb3+ doping which causes multicolour emissions from nano-phosphor. The intensity of UC red emission (654 nm) obtained from 1 at.% Ho3+ and 3 at.% Yb3+ co-doped nano-phosphor is nine times higher than from 1 at.% Ho3+ doped SrSnO3 nano-phosphor. Enhanced brightness of 654 nm in UC process belongs in biological transparency window so that it might be a promising phosphor in the bio-medical field. Moreover, for the other Yb3+ co-doped nano-phosphor, Commission Internationale de l'Éclairage chromaticity co-ordinates were found near the white region and their CCT values lie in the range 4900-5100 K indicating cool white. Decay time was measured for 545 nm emission of Ho3+ ion found in 7.652 and 8.734 µs at 355 nm excitation. The variation in lifetime was observed in ascending order with increasing Yb3+ concentration which supports PL emission spectra observation that with increasing Yb3+ concentration, rate of transition has changed. These studies reveal that Ho3+ and Yb3+ co-doped phosphor is useful for fabrication of white LEDs.

Eu/Tb ions co-doped white light luminescence Y2O3 phosphors

International Nuclear Information System (INIS)

Tu Dong; Liang Yujun; Liu Rong; Li Daoyi

2011-01-01

Y 2 O 3 :Eu 3+ , Tb 3+ phosphors with white emission are prepared with different doping concentration of Eu 3+ and Tb 3+ ions and synthesizing temperatures from 750 to 950 deg. C by the co-precipitation method. The resulted phosphors were characterized by X-ray diffraction (XRD) and photoluminescence (PL) spectroscopy. The results of XRD indicate that the crystallinity of the synthesized samples increases with enhancing the firing temperature. The photoluminescence spectra indicate the Eu 3+ and Tb 3+ co-doped Y 2 O 3 phosphors show five main emission peaks: three at 590, 611 and 629 nm originate from Eu 3+ and two at 481 and 541 nm originate from Tb 3+ , under excitation of 250-320 nm irradition. The white light luminescence color could be changed by varying the excitation wavelength. Different concentrations of Eu 3+ and Tb 3+ ions were induced into the Y 2 O 3 lattice and the energy transfer from Tb 3+ →Eu 3+ ions in these phosphors was found. The Commission International de l'Eclairage (CIE) chromaticity shows that the Y 2 O 3 :Eu 3+ , Tb 3+ phosphors can obtain an intense white emission. - Highlights: → Novel phosphors Y 2 O 3 :Eu 3+ , Tb 3+ have been synthesized by co-precipitation method. → Samples emit white light with excellent color coordinates under UV excitation. → Luminescence color could be changed by varying the excitation wavelength. → Energy transfer from Tb 3+ →Eu 3+ ions in these phosphors was found.

Photoluminescent and Thermoluminescent Studies of Dy3+ and Eu3+ Doped Y2O3 Phosphors.

Science.gov (United States)

Verma, Tarkeshwari; Agrawal, Sadhana

2018-01-01

Eu 3+ doped and Dy 3+ codoped yttrium oxide (Y 2 O 3 ) phosphors have been prepared using solid-state reaction technique (SSR). The prepared phosphors were characterized by X-ray diffractometer (XRD), energy dispersive X-ray (EDX) spectroscopy, scanning electron microscopy (SEM) and Fourier transforms infrared spectroscopy (FTIR) techniques. Photoluminescence (PL) and Thermoluminescence (TL) properties were studied in detail. PL emission spectra were recorded for prepared phosphors under excitation wavelength 254 nm, which show a high intense peak at 613 nm for Y 2 O 3 :Dy 3+ , Eu 3+ (1:1.5 mol %) phosphor. The correlated color temperature (CCT) and CIE analysis have been performed for the synthesized phosphors. TL glow curves were recorded for Eu 3+ doped and Dy 3+ codoped phosphors to study the heating rate effect and dose response. The kinetic parameters were calculated using peak shape method for UV and γ exposures through computerized glow curve deconvolution (CGCD) technique. The phosphors show second order kinetics and activation energies varying from 5.823 × 10 - 1 to 18.608 × 10 - 1  eV.

Luminescence properties of Sm{sup 3+}-doped Sr{sub 3}Sn{sub 2}O{sub 7} phosphor

Energy Technology Data Exchange (ETDEWEB)

Lei Bingfu, E-mail: tleibf@jnu.edu.cn [Department of Physics, Jinan University, Guangzhou 510632 (China); Department of Chemistry and Nanochemistry Institute, Jinan University, Guangzhou 510632 (China); Man Shiqing [Department of Chemistry and Nanochemistry Institute, Jinan University, Guangzhou 510632 (China); Department of Electronic Engineering, Jinan University, Guangzhou 510632 (China); Liu Yingliang [Department of Chemistry and Nanochemistry Institute, Jinan University, Guangzhou 510632 (China); Yue Song [Department of Physics, Jinan University, Guangzhou 510632 (China)

2010-12-01

We report on a luminescent phenomenon in Sm{sup 3+}-doped Sr{sub 3}Sn{sub 2}O{sub 7} afterglow phosphor. XRD, photoluminescence, afterglow emission spectra and long-lasting phosphorescence decay curve are used to characterize this phosphor. After irradiation by a 267-nm UV light for 5 min, the Sm{sup 3+}-doped Sr{sub 3}Sn{sub 2}O{sub 7} phosphor emits intense reddish-orange emitting afterglow from the {sup 4}G{sub 5/2} to {sup 6}H{sub J} (J = 5/2, 7/2, 9/2) transitions, and its afterglow can be seen with the naked eye in the dark clearly for more than 1 h after removal of the excitation source. Photoluminescence spectra reveal that the reddish-orange light-emitting long-lasting phosphorescence originate from the mixture of Sm{sup 3+} characteristic transitions. The afterglow decay curve of the Sm{sup 3+}-doped Sr{sub 3}Sn{sub 2}O{sub 7} phosphor contains a fast decay component and another slow decay one. The possible mechanism of this reddish-orange light-emitting LLP phosphor is also discussed based on the experiment results.

Studies in crystal structure and luminescence properties of Eu3+-doped metal tungstate phosphors for white LEDs

International Nuclear Information System (INIS)

Lee, Gwan-Hyoung; Kang, Shinhoo

2011-01-01

The correlation between the crystal structure and luminescent properties of Eu 3+ -doped metal tungstate phosphors for white LEDs was investigated. Red-emitting A 4-3x (WO 4 ) 2 :Eu x 3+ (A=Li, Na, K) and B (4-3x)/2 (WO 4 ) 2 :Eu x 3+ (B=Mg, Ca, Sr) phosphors were synthesized by solid-state reactions. The findings confirmed that these phosphors exhibited a strong absorption in the near UV to green range, due to the intra-configurational 4f-4f electron transition of Eu 3+ ions. The high doping concentration of Eu 3+ enhanced the absorption of near UV light and red emission without any detectable concentration quenching. Based on the results of a Rietveld refinement, it was attributed to the unique crystal structure. In the crystal structure of the Eu 3+ -doped metal tungstate phosphor, the critical energy transfer distance is larger than 5 A so that exchange interactions between Eu 3+ ions would occur with difficulty, even at a high doping concentration. The energy transfer between Eu 3+ ions, which causes a decrease in red emission with increasing concentration of Eu 3+ , appears to be due to electric multi-polar interactions. In addition, the Eu-O distance in the host lattice affected the shape of emission spectrum by splitting of emission peak at the 5 D 0 → 7 F 2 transition of Eu 3+ . - Highlights: → Eu 3+ -doped metal tungstate was synthesized as a red phosphor for white LEDs. → Crystal structure is tetragonal with a space group of I4 1 /c. → A strong absorption in the near UV to green range was observed. → High doping of Eu 3+ enhanced the absorption of near UV light and red emission.

Photoluminescence and thermoluminescence properties of Eu2+ doped and Eu2+ ,Dy3+ co-doped Ba2 MgSi2 O7 phosphors.

Science.gov (United States)

Sao, Sanjay Kumar; Brahme, Nameeta; Bisen, D P; Tiwari, Geetanjali

2016-11-01

In this work, we report the preparation, characterization, comparison and luminescence mechanisms of Eu 2 + -doped and Eu 2 + ,Dy 3 + -co-doped Ba 2 MgSi 2 O 7 (BMSO) phosphors. Prepared phosphors were synthesized via a high temperature solid-state reaction method. All prepared phosphors appeared white. The phase structure, particle size, and elemental analysis were analyzed using X-ray diffraction (XRD), transmission electron microscopy (TEM) and energy-dispersive X-ray (EDX) analysis. The luminescence properties of the phosphors were investigated by thermoluminescence (TL) and photoluminescence (PL). The PL excitation and emission spectra of Ba 2 MgSi 2 O 7 :Eu 2 + showed the peak to be around 381 nm and 490 nm respectively. The PL excitation spectrum of Ba 2 MgSi 2 O 7 :Eu 2 + Dy 3 + showed the peak to be around 341 nm and 388 nm, and the emission spectrum had a broad band around 488 nm. These emissions originated from the 4f 6 5d 1 to 4f 7 transition of Eu 2 + . TL analysis revealed that the maximum TL intensity was found at 5 mol% of Eu 2 + doping in Ba 2 MgSi 2 O 7 phosphors after 15 min of ultraviolet (UV) light exposure. TL intensity was increased when Dy 3 + ions were co-doped in Ba 2 MgSi 2 O 7 :Eu 2 + and maximum TL intensity was observed for 2 mol% of Dy 3 + . TL emission spectra of Ba 1.95 MgSi 2 O 7 :0.05Eu 2 + and Ba 1.93 MgSi 2 O 7 :0.05Eu 2 + ,0.02Dy 3 + phosphors were found at 500 nm. TL intensity increased with UV exposure time up to 15 min, then decreased for the higher UV radiation dose for both Eu doping and Eu,Dy co-doping. The trap depths were calculated to be 0.54 eV for Ba 1.95 MgSi 2 O 7 :0.05Eu 2 + and 0.54 eV and 0.75 eV for Ba 1.93 MgSi 2 O 7 :0.05Eu 2 + ,0.02Dy 3 + phosphors. It was observed that co-doping with small amounts of Dy 3 + enhanced the thermoluminescence properties of Ba 2 MgSi 2 O 7 phosphor. Copyright © 2016 John Wiley & Sons, Ltd. [Correction added on 5 April 2016, after first online publication: The

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)

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

Enhanced red emission of LaVO{sub 4}:Eu{sup 3+} phosphors by Li-doping

Energy Technology Data Exchange (ETDEWEB)

Park, Sung Wook; Yang, Hyun Kyoung; Chung, Jong Won; Moon, Byung Kee; Choi, Byung Chun; Jeong, Jung Hyun [Pukyoung National University, Busan (Korea, Republic of); Jang, Ki Wan; Lee, Ho Sueb [Changwon National University, Changwon (Korea, Republic of); Yi, Soung Soo [Silla University, Busan (Korea, Republic of)

2010-12-15

LaVO{sub 4} phosphors were synthesized by using a solid state reaction, and were characterized by using X-ray diffraction (XRD), scanning electron microscopy (SEM) and photoluminescence (PL). The XRD patterns of the Li-doped LaVO{sub 4}:Eu{sup 3+} powder phosphors revealed a mixture of tetragonal and monoclinic phases. The tetragonal phase of the LaVO{sub 4}:Eu{sup 3+} phosphor showed a higher PL intensity than the monoclinic one, despite the presence of both monoclinic and tetragonal structures. The Li-doped LaVO{sub 4}:Eu{sup 3+} powder phosphors absorbed strongly at 396 nm and exhibited strong red emission at approximately 619.5 nm due to the {sup 5}D{sub 0} {yields} {sup 7}F{sub 2} transition. The incorporation of Li{sup +} ions into the LaVO{sub 4}:Eu{sup 3+} powder can lead to a remarkable increase in photoluminescence. The enhanced luminescence is attributed to the incorporation of Li{sup +} ions that may act as a sensitizers for effective energy transfer. This phosphor has promising applications in near-UV light-emitting diodes(LEDs).

Enhanced luminescence properties of YBO{sub 3}:Eu{sup 3+} phosphors by Li-doping

Energy Technology Data Exchange (ETDEWEB)

Balakrishnaiah, R. [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Yi, Soung Soo, E-mail: ssyi@silla.ac.kr [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Jang, Kiwan; Lee, Ho Sueb [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Moon, Byung Kee; Jeong, Jung Hyun [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of)

2011-04-15

Different concentrations of Li-doped YBO{sub 3}:Eu{sup 3+} phosphors have been prepared by the conventional solid state reaction method and were characterized by X-ray diffraction, field emission scanning electron microscopy, photoluminescence excitation and emission measurements. An intense reddish orange emission is observed under UV excitation and the emitted radiation was dominated by an orange peak at 594 nm resulted from the {sup 5}D{sub 0} {yields} {sup 7}F{sub 1} transitions of Eu{sup 3+} ions. The brightness of the YBO{sub 3}:Eu{sup 3+} phosphor was found greatly improved with Li-doping accompanied by slight improvement in the purity of the color which might be attributed to improvement in crystallinity, grain sizes and creation of oxygen vacancies with Li-doping. The observed results have been discussed in comparison with similar reported works.

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.

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....

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

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

Ce3+-Doped garnet phosphors : Composition modification, luminescence properties and applications

NARCIS (Netherlands)

Xia, Zhiguo; Meijerink, Andries

2017-01-01

Garnets have the general formula of A3B2C3O12 and form a wide range of inorganic compounds, occurring both naturally (gemstones) and synthetically. Their physical and chemical properties are closely related to the structure and composition. In particular, Ce3+-doped garnet phosphors have a long

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

Structural and optical properties of Tb and Na-Tb co-doped Ca3V2O8 phosphors prepared by sol-gel process

Science.gov (United States)

Parab, Shambhu S.; Salker, A. V.

2018-01-01

A malic acid assisted sol-gel route was successfully employed to prepare two distinct series of green emitting Ca3V2O8 phosphors. In the first series, Tb was solely doped whereas in the second series Na and Tb were doped simultaneously in the Ca3V2O8 crystal lattice. X-ray diffraction studies proved the utility of adopted preparative method by confirming the monophasic formation of all compounds from both the series. Spectral analysis like Raman spectroscopy, UV-DRS were undertaken to analyse the local structure, crystallinity and absorptive characteristics. XPS validated the presence of desired oxidation states of all the elements present. Finally, photoluminescence studies were done to elucidate the scope of prepared compounds as green emitting phosphors and also to understand the effect of both doping schemes on the luminescence. Intense green emission was observed in both the cases. Tb concentration of 0.08 was found to be optimum in case of Tb singly doped compounds whereas Tb = 0.12 showed highest intensity among the Na-Tb co-doped samples. Moreover, a red shift in the excitation wavelength was observed after Na doping signifying a change in the local electronic environment which in turn has affected the luminescence pattern. Local crystallinity and vacancy concentrations were found to have a major say on the emission intensities.

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.

Luminescence enhancement in Eu3+, Sm3+ co-doped liy(MoO4)2 nano-phosphors by sol-gel process.

Science.gov (United States)

Zhou, Xianju; Wang, Guangchuan; Zhou, Tonghui; Zhou, Kaining; Li, Qingxu; Wang, Zhongqing

2014-05-01

A series of LiY(0.95-x)Eu(0.05)Sm(x)(MoO4)2 red light emitting phosphors were synthesized by sol-gel technique. The phase impurity and spectroscopic properties were characterized by X-ray Diffraction (XRD), Photo-Luminescence (PL) and Photo-Luminescence Excitation (PLE) spectra, respectively. It is found that the PLE spectra of the Eu3+, Sm3+ co-doped nanoparticles are enhanced and broadened as compared with the solely doped samples, which will make the co-doped phosphors match better with blue and/or UV GaN based LED chips. The red emission intensity of Eu3+ is largely enhanced by the energy transfer from Sm3+. The mechanism of the enhancement is clearly proven to be the increase in the quantum efficiency of 5D0 state of Eu3+ rather than the increase in the absorption of Eu3+. Meanwhile, the characteristic f-f transitions of Sm3+ are greatly reduced, resulting in little influence in the color purity of the co-doped phosphors. The present material is an amendatory promising red light emitting phosphor for white LEDs.

Photovoltaic Performance Enhancement of Silicon Solar Cells Based on Combined Ratios of Three Species of Europium-Doped Phosphors.

Science.gov (United States)

Ho, Wen-Jeng; You, Bang-Jin; Liu, Jheng-Jie; Bai, Wen-Bin; Syu, Hong-Jhang; Lin, Ching-Fuh

2018-05-18

This paper presents a scheme for the enhancement of silicon solar cells in terms of luminescent emission band and photovoltaic performance. The proposed devices are coated with an luminescent down-shifting (LDS) layer comprising three species of europium (Eu)-doped phosphors mixed within a silicate film (SiO₂) using a spin-on film deposition. The three species of phosphor were mixed at ratios of 0.5:1:1.5, 1:1:1, or 1.5:1:0.5 in weight percentage (wt %). The total quantity of Eu-doped phosphors in the silicate solution was fixed at 3 wt %. The emission wavelengths of the Eu-doped phosphors were as follows: 518 nm (specie-A), 551 nm (specie-B), and 609 nm (specie-C). We examined the extended luminescent emission bands via photoluminescence measurements at room temperature. Closely matching the luminescent emission band to the high responsivity band of the silicon semiconductor resulted in good photovoltaic performance. Impressive improvements in efficiency were observed in all three samples: 0.5:1:1.5 (20.43%), 1:1:1 (19.67%), 1.5:1:0.5 (16.81%), compared to the control with a layer of pure SiO₂ (13.80%).

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.)

NIR optimized dual mode photoluminescence in Nd doped Y{sub 2}O{sub 3} ceramic phosphor

Energy Technology Data Exchange (ETDEWEB)

Sukul, Prasenjit Prasad; Mahata, Manoj Kumar; Kumar, Kaushal, E-mail: kumar.bhu@gmail.com

2017-05-15

Authors here report the dual mode photo luminescence emission in neodymium doped yttrium oxide ceramic phosphor upon 808 nm diode laser excitation. Single cubic phase Nd{sup 3+} doped Y{sub 2}O{sub 3} phosphor was synthesized using urea assisted combustion route. Nd{sup 3+} doped Y{sub 2}O{sub 3} ceramic phosphor has given photoluminescence in a wide wavelength range covering near infrared window (850–1100 nm) to the visible region i.e. green (525 nm) and red (680 nm) upon 808 nm diode laser excitation. The two most intense bands on 808 nm excitation were observed at 750 nm and 1064 nm due to the upconversion and downconversion emission processes. The sample was also tested for emission using 980 nm and intense green emission due to the trace presence of Er{sup 3+} in the raw materials was seen in the sample. The excitation power dependent upconversion measurements have shown that transitions {sup 4}F{sub 9/2}→{sup 4}I{sub 9/2} and {sup 4}S{sub 3/2}→{sup 4}I{sub 9/2} are thermally coupled and can be used to estimate the sample temperature using Boltzmann relation.

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

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.

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)

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.

Photocatalytic characteristics for the nanocrystalline TiO{sub 2} on the Ag-doped CaAl{sub 2}O{sub 4}:(Eu,Nd) phosphor

Energy Technology Data Exchange (ETDEWEB)

Kim, Jung-Sik, E-mail: jskim@uos.ac.kr; Sung, Hyun-Je; Kim, Bum-Joon

2015-04-15

Highlights: • The photocatalytic reactivity of the TiO{sub 2}-coated on the Ag-doped long-lasting phosphor (CaAl{sub 2}O{sub 4}:Eu{sup 2+},Nd{sup 3+}). • The photodecomposition of benzene gas under visible light irradiation. • The TiO{sub 2}-coated on the Ag-doped long-lasting phosphor showed much higher photocatalytic reactivity. • The light emitted from the long-lasting phosphors contributed to the photo generation of TiO{sub 2}. - Abstract: This study investigated the photocatalytic behavior of nanocrystalline TiO{sub 2} deposited on Ag-doped long-lasting phosphor (CaAl{sub 2}O{sub 4}:Eu{sup 2+},Nd{sup 3+}). The CaAl{sub 2}O{sub 4}:Eu{sup 2+},Nd{sup 3+} phosphor powders were prepared via conventional sintering using CaCO{sub 3}, Al{sub 2}O{sub 3}, Eu{sub 2}O{sub 3}, and Nd{sub 2}O{sub 3} as raw materials according to the appropriate molar ratios. Silver nanoparticles were loaded on the phosphor by mixing with an aqueous Ag-dispersion solution. Nanocrystalline TiO{sub 2} was deposited on Ag-doped CaAl{sub 2}O{sub 4}:Eu{sup 2+},Nd{sup 3+} powders via low-pressure chemical vapor deposition (LPCVD). The TiO{sub 2} coated on the phosphor was actively photo-reactive under irradiation with visible light and showed much faster benzene degradation than pure TiO{sub 2}, which is almost non-reactive. The coupling of TiO{sub 2} with phosphor may result in an energy band bending in the junction region, which then induces the TiO{sub 2} crystal at the interface to be photo-reactive under irradiation with visible light. In addition, the intermetallic compound of CaTiO{sub 3} that formed at the interface between TiO{sub 2} and the CaAl{sub 2}O{sub 4}:(Eu{sup 2+},Nd{sup 3+}) phosphor results in the formation of oxygen vacancies and additional electrons that promote the photodecomposition of benzene gas. The addition of Ag nanoparticles enhanced the photocatalytic reactivity of the TiO{sub 2}/CaAl{sub 2}O{sub 4}:Eu{sup 2+},Nd{sup 3+} phosphor. TiO{sub 2} on the Ag-doped

Improved efficiency of dye-sensitized solar cells by doping of strontium aluminate phosphor in TiO2 photoelectrode

Directory of Open Access Journals (Sweden)

Hwangbo Seung

2015-06-01

Full Text Available SrAl2O4:Eu2+, Dy3+ phosphor was synthesized by chemical solution route to use as a dopant in TiO2 layer employed as a photoelectrode for down conversion of ultraviolet and near-ultraviolet to visible and near-infrared light in a dye-sensitized solar cell. Nano-crystalline structure of the SrAl2O4:Eu2+, Dy3+ powder was confirmed by X-ray diffraction analysis and field emission scanning electron microscopy. Monitored at 520 nm, SrAl2O4:Eu2+, Dy3+ phosphor showed emission peaks at 460 to 610 nm due to 4f6 4f7 transitions of Eu2+ ions. For the study, SrAl2O4:Eu2+, Dy3+ phosphor-doped TiO2 layer was deposited on fluorine-doped tin oxide coated glass by electrostatic spray deposition. The short circuit current, open circuit voltage, fill factor, and conversion efficiency of the cells were measured. Experimental results revealed that the device efficiency for the SrAl2O4:Eu2+, Dy3+ phosphor-doped TiO2 layer increased to 7.20 %, whereas that of the pure-TiO2 photoelectrode was 4.13 %.

Photovoltaic Performance Enhancement of Silicon Solar Cells Based on Combined Ratios of Three Species of Europium-Doped Phosphors

Directory of Open Access Journals (Sweden)

Wen-Jeng Ho

2018-05-01

Full Text Available This paper presents a scheme for the enhancement of silicon solar cells in terms of luminescent emission band and photovoltaic performance. The proposed devices are coated with an luminescent down-shifting (LDS layer comprising three species of europium (Eu-doped phosphors mixed within a silicate film (SiO2 using a spin-on film deposition. The three species of phosphor were mixed at ratios of 0.5:1:1.5, 1:1:1, or 1.5:1:0.5 in weight percentage (wt %. The total quantity of Eu-doped phosphors in the silicate solution was fixed at 3 wt %. The emission wavelengths of the Eu-doped phosphors were as follows: 518 nm (specie-A, 551 nm (specie-B, and 609 nm (specie-C. We examined the extended luminescent emission bands via photoluminescence measurements at room temperature. Closely matching the luminescent emission band to the high responsivity band of the silicon semiconductor resulted in good photovoltaic performance. Impressive improvements in efficiency were observed in all three samples: 0.5:1:1.5 (20.43%, 1:1:1 (19.67%, 1.5:1:0.5 (16.81%, compared to the control with a layer of pure SiO2 (13.80%.

Luminescent features of sol–gel derived rare-earth multi-doped oxyfluoride nano-structured phosphors for white LED application

International Nuclear Information System (INIS)

Gouveia-Neto, A.S.; Silva, A.F. da; Bueno, L.A.; Costa, E.B. da

2012-01-01

Rare-earth doped oxyfluoride 75SiO 2 :25PbF 2 nano-structured phosphors for white-light-emitting diodes were synthesized by thermal treatment of precursor sol–gel derived glasses. Room temperature luminescence features of Eu 3+ , Sm 3+ , Tb 3+ , Eu 3+ /Tb 3+ , and Sm 3+ /Tb 3+ ions incorporated into low-phonon-energy PbF 2 nanocrystals dispersed in the aluminosilicate glass matrix and excited with UV light emitting diode were investigated. The luminescence spectra exhibited strong emission signals in the red (600, 610, 625, and 646 nm), green (548 and 560 nm), and blue (485 nm) wavelength regions. White-light emission was observed in Sm/Tb and Eu/Tb double-doped activated phosphors employing UV-LED excitation at 395 nm. The dependence of the luminescence emission intensities upon annealing temperature and rare-earth concentration was also examined. The results indicated that there exist optimum annealing temperature and activator ion concentration in order to obtain intense visible emission light with high color rendering index. The study suggests that the nanocomposite phosphor based upon 75SiO 2 :25PbF 2 host herein reported is a promising contender for white-light LED applications. - Highlights: ► White-light emission in double-doped activated phosphors employing UV-LED excitation. ► Luminescent features of europium, samarium, and terbium in nanocrystals dispersed in aluminosilicate glass. ► New nanocomposite phosphor host for white-light LED applications.

Luminescence in Eu2+ and Ce3+ doped SrCaP2O7 phosphors

Directory of Open Access Journals (Sweden)

K.N. Shinde

Full Text Available Eu2+ and Ce3+ doped SrCaP2O7 has been achieved by modified solid state diffusion in reducing atmosphere. The prepared phosphor powders have been identified by their characteristic X-ray diffraction patterns. The mixed phases of α-Sr2P2O7 type with orthorhombic and α-Ca2P2O7 type with monoclinic form were investigated. Its excitation wavelength ranging from 250 to 430 nm fits well with the characteristic emission of UV light-emitting diode (LED. The excitation and emission spectra indicate that these phosphors can be effectively excited by the near-UV light, and emits blue (visible range due to 4f7 → 4f65d1 transition of Eu2+ particularly, SrCaP2O7: Eu2+ whereas, photoluminescence excitation spectrum measurements of Ce3+ activated SrCaP2O7 shows that the phosphor can be efficiently excited by UV–Vis light from 280 to 310 nm to realize emission in the near visible range due to the 5d–4f transition of Ce3+ ions which is applicable for scintillation purpose. The impacts of doping of divalent europium and trivalent cerium on photoluminescence properties on SrCaP2O7 pyrophosphate phosphors were investigated and I propose a feasible interpretation. Keywords: Phosphor, Luminescence, XRD, LED, FTIR

Long afterglow property of Er{sup 3+} doped Ca{sub 2}SnO{sub 4} phosphor

Energy Technology Data Exchange (ETDEWEB)

Zhang, Dongyun, E-mail: dyz@sit.edu.cn; Shi, Mingming; Sun, Yiwen; Guo, Yunyun; Chang, Chengkang

2016-05-15

A novel green emitting long afterglow phosphor, Er{sup 3+} -doped Ca{sub 2}SnO{sub 4} (Ca{sub 2}SnO{sub 4}:Er{sup 3+}), was prepared successfully via a traditional high temperature solid–state reaction method. Its properties have been characterized and analyzed by utilizing x-ray diffraction (XRD), photoluminescence spectroscope (PLS), afterglow decay curve (ADC) and thermal luminescence spectroscope (TLS). Three main emission peaks of PLS locate at 524, 550 and 668 nm, corresponding to CIE chromaticity coordinates of x = 0.326, y = 0.6592. An optimal doping concentration of Er{sup 3+} of 2% was determined. The Ca{sub 2}SnO{sub 4}:Er{sup 3+} phosphors showed a typical triple-exponential afterglow decay behavior when the UV source was switched off. Thermal simulated luminescence study indicated that the persistent afterglow of Ca{sub 2}SnO{sub 4}:2 mol% Er{sup 3+} phosphors was generated by the suitable electron or hole traps which were resulted from the doping the Ca{sub 2}SnO{sub 4} host with rare-earth ions (Er{sup 3+}). - Highlights: • A novel green emitting long afterglow phosphor, Ca{sub 2}SnO{sub 4}:Er{sup 3+}, was prepared. • An optimal doping concentration of Er{sup 3+} of 2% was determined. • After the UV source was turned off, the Ca{sub 2}SnO{sub 4}:Er{sup 3+} showed a typical triple-exponential afterglow decay behavior. • CIE chromaticity coordinates results confirmed a green light emitting of the Ca{sub 2}SnO{sub 4}:Er{sup 3+}. • The persistent afterglow of the Ca{sub 2}SnO{sub 4}:Er{sup 3+} was attributed to suitable electron or hole traps.

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

Photoluminescence in Sm3+ doped Ba2P2O7 phosphor prepared by solution combustion method

Science.gov (United States)

Ghawade, Sonal P.; Deshmukh, Kavita A.; Dhoble, S. J.; Deshmukh, Abhay D.

2018-05-01

In this paper, Sm3+ doped Ba2P2O7 phosphors were synthesized via a Solution combustion method. The crystal structure of the phosphor was characterized by XRD. Orange-red emission was observed from these phosphors under near-ultraviolet (UV) excitation at 404 nm. The luminescence properties of the obtained phosphors were characterized by different techniques. The Ba2P2O7:Sm3+ phosphor can be efficiently excited by near-UV and blue light, and their emission spectrum consists of three emission peaks, at 564, 602, and 646 nm, respectively. Based on the results, the as prepared Ba2P2O7:Sm3+ phosphors are promising orange-red-emitting phosphors exhibit great potential may be applicable as a spectral convertor in c-Si solar cell to enhance the efficiency of solar cell in future.

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

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.

Photoluminescence characteristics of reddish-orange Eu{sup 3+} or Sm{sup 3+} singly-doped and Eu{sup 3+} and Sm{sup 3+} co-doped KZnGd(PO{sub 4}){sub 2} phosphors

Energy Technology Data Exchange (ETDEWEB)

Jeong, Jun Ho; Bandi, Vengala Rao; Grandhe, Bhaskar Kumar; Jang, Ki Wan; Lee, Ho Sueb [Changwon National University, Changwon (Korea, Republic of); Yi, Soung Soo [Silla University, Busan (Korea, Republic of); Jeong, Jung Hyun [Pukyong National University, Busan (Korea, Republic of)

2011-02-15

Eu{sup 3+} or Sm{sup 3+} singly-doped and Eu{sup 3+} and Sm{sup 3+} co-doped KZnGd(PO{sub 4}){sub 2} phosphors were synthesized by using a conventional solid state reaction method at 750 .deg. C. The emission spectra of KZnGd{sub 1-x}(PO{sub 4}){sub 2}:Eu{sup 3+}{sub x} with {lambda}{sub ex} = 395 nm and KZnGd{sub 1-y}(PO{sub 4}){sub 2}:Sm{sup 3+}{sub y} with {lambda}{sub ex} = 403 nm phosphors showed intense {sup 5}D{sub 0} {yields} {sup 7}F{sub 1}, {sup 4}G{sub 5/2} {yields} {sup 6}H{sub 7/2} emission transitions at 595 nm and 599 nm, respectively. The optimum relative intensity of the KZnGd{sub 1-x-y}(PO{sub 4}){sub 2}:Eu{sup 3+}{sub x} , Sm{sup 3+}{sub y} phosphor was obtained for the doping concentrations of (x = 0.09, y = 0.01). In addition, the temperature dependent luminescence intensity of the synthesized phosphors was investigated and the thermal stability of the KZnGd(PO{sub 4}){sub 2}:Eu{sup 3+} phosphor was found to be higher than that of standard YAG:Ce{sup 3+} and KZnGd{sub 1-x-y}(PO{sub 4}){sub 2}:Eu{sup 3+}{sub x} Sm{sup 3+}{sub y} under near ultra-violet (NUV) light emitting diode excitation (LED). Therefore, we suggest that Eu{sup 3+} or Sm{sup 3+} singly-doped and Eu{sup 3+} and Sm{sup 3+} co-doped KZnGd(PO{sub 4}){sub 2} phosphors should be efficient for different red-color-emitting display device applications and NUV-LED-based white-light-emitting diodes.

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

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

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.

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)

Recent advances in enhanced luminescence upconversion of lanthanide-doped NaYF4 phosphors

Science.gov (United States)

Kumar, Deepak; Verma, Kartikey; Verma, Shefali; Chaudhary, Babulal; Som, Sudipta; Sharma, Vishal; Kumar, Vijay; Swart, Hendrik C.

2018-04-01

NaYF4 is regarded as the best upconversion (UC) matrix owing to its low phonon energy, more chemical stability, and a superior refractive index. This review reports on the various synthesis techniques of lanthanide-doped NaYF4 phosphors for UC application. The UC intensity depends on different properties of the matrix and those are discussed in detail. Plasmon-enhanced luminescence UC of the lanthanide-doped NaYF4 core-shells structure is discussed based on a literature survey. The present review provides the information about how the UC intensity can be enhanced. The idea about the UC is then deliberately used for versatile applications such as luminescent materials, display devices, biomedical imaging and different security appliances. In addition, the present review demonstrates the recent trends of NaYF4 UC materials in solar cell devices. The role of NaYF4 phosphor to eradicate the spectral variance among the incident solar spectrum, semiconductor as well as the sub-band gap nature of the semiconductor materials is also discussed in detail. Considering the fact that the research status on NaYF4 phosphor for photovoltaic application is now growing, the present review is therefore very important to the researchers. More importantly, this may promote more interesting research platforms to investigate the realistic use of UC nanophosphors as spectral converters for solar cells.

White- and blue-light-emitting dysprosium(III) and terbium(III)-doped gadolinium titanate phosphors.

Science.gov (United States)

Antić, Ž; Kuzman, S; Đorđević, V; Dramićanin, M D; Thundat, T

2017-06-01

Here we report the synthesis and structural, morphological, and photoluminescence analysis of white- and blue-light-emitting Dy 3 + - and Tm 3 + -doped Gd 2 Ti 2 O 7 nanophosphors. Single-phase cubic Gd 2 Ti 2 O 7 nanopowders consist of compact, dense aggregates of nanoparticles with an average size of ~25 nm for Dy 3 + -doped and ~50 nm for Tm 3 + -doped samples. The photoluminescence results indicated that ultraviolet (UV) light excitation of the Dy 3 + -doped sample resulted in direct generation of white light, while a dominant yellow emission was obtained under blue-light excitation. Intense blue light was obtained for Tm 3 + -doped Gd 2 Ti 2 O 7 under UV excitation suggesting that this material could be used as a blue phosphor. Copyright © 2016 John Wiley & Sons, Ltd.

Synthesis and luminescence properties of Ce{sup 3+} doped MWO{sub 4} (M=Ca, Sr and Ba) microcrystalline phosphors

Energy Technology Data Exchange (ETDEWEB)

Dabre, K.V. [Department of Physics, Arts, Commerce and Science College, Koradi, Nagpur (India); Dhoble, S.J., E-mail: sjdhoble@rediffmail.com [Department of Physics, R.T.M. Nagpur University, Nagpur 440033 (India); Lochab, Jyoti [Radiotherapy Department, Safdarjung Hospital, New Delhi (India)

2014-05-01

The Ce{sup 3+} doped and undoped samples of alkali earth metal tungstate MWO{sub 4} (M=Ca, Sr, and Ba) phosphors are synthesized by a co-precipitation method in controlled pH environment. The resulting phosphors were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Fourier transform infrared (FTIR), photoluminescence (PL) and thermoluminescence (TL). XRD pattern and SEM micrographs reveal the formation of agglomerated microcrystalline phosphor. FTIR spectra show the strong absorption around 821 cm{sup −1} due to characteristic vibrations of (WO{sub 4}){sup 2−} complex. PL excitation spectra show broadband in the UV region having peak at 280 nm, and the emission spectrum shows broadband in the visible region with peak in the blue region. The PL emission intensity increases with Ce{sup 3+} concentration with the most effective concentration at 5 mol%. The complex TL glow curve of Ce{sup 3+} doped phosphors is deconvoluted by using a TLAnal computer program. The trap parameters obtained by TLAnal were compared with those calculated by Chen's method and a possible model for TL is discussed. - Highlights: • M{sub 1−x}WO{sub 4}:Ce{sub x} (M=Ca, Sr, and Ba) phosphors are synthesized by the co-precipitation method in controlled pH environment. • Phosphor exhibits broad emission band with maximum in the blue region. • Enhancement of PL emission intensity due to doping of Ce in a host lattice. • The complex TL glow curves were deconvoluted by TLAnal. • FTIR spectra show the main transmittance peaks related to v{sub 3} and v{sub 4} vibration modes of W–O bonds.

Co-operative energy transfer in Yb3+-Er3+ co-doped SrGdxOy upconverting phosphor

Science.gov (United States)

Kumar, Ashwini; Pathak, Trilok K.; Dhoble, S. J.; . Terblans, J. J.; Swart, H. C.

2018-04-01

Upconversion nanoparticles (UCNPs) have shown considerable interest in many fields; however, low upconversion efficiency of UCNPs is still the most severe limitation of their applications. Yb3+ and Er3+ co-doped SrGd4O7/Gd2O3(SGO) upconversion (UC) phosphors were synthesized by a modified co-precipitation process. The UC properties were investigated by direct excitation with a 980 nm laser. It was observed that the as prepared materials showed relatively strong green emission, while upon the incorporation of the Er3+ ion, there was an increase in the upconversion luminescence intensity for the red component. The effect of different doping concentration of Er3+on the emission spectra and X-ray diffraction patterns of the UC materials have also been studied. The luminescence lifetimes and Commission Internationale de L'Eclairage coordinates for these as prepared samples were determined to understand the energy transfer (ET) mechanisms occurring between Yb3+ and Er3+ in the SGO host matrix. The UC luminescence intensity as a function of laser pump power was monitored and it was confirmed that the UC process in SGO:Yb3+/Er3+is a two-photon absorption process. The findings reported here are expected to provide a better approach for understanding of the ET mechanisms in the oxide based Yb3+/Er3+ co-doped UC phosphors. This study might be helpful in precisely defined applications where optical transitions are essential criterion and this can be easily achieved by smart tuning of the emission properties of Yb3+/Er3+ co-doped UC phosphors.

Oxidative degradation of acid doped polybenzimidazole membranes and fuel cell durability in the presence of ferrous ions

DEFF Research Database (Denmark)

Liao, Jianhui; Yang, Jingshuai; Li, Qingfeng

2013-01-01

Phosphoric acid doped polybenzimidazole membranes have been explored as proton exchange membranes for high temperature polymer electrolyte membrane fuel cells. Long-term durability of the membrane is of critical concern and has been evaluated by accelerated degradation tests under Fenton conditions...... of the polymer. Fuel cell durability tests with contaminations of ferrous ions did show considerable performance degradation, however, primarily due to the catalyst deterioration rather than the membrane degradation........ In this study effects of phosphoric acid and ferrous ions were investigated by measurements of the weight loss, intrinsic viscosity and size exclusion chromatography (SEC) of the polymer membranes. Ferrous ions resulted in, as expected, catalytic formation of peroxide radicals and hence the accelerated polymer...

Using rare earth doped thiosilicate phosphors in white light emitting LEDs: Towards low colour temperature and high colour rendering

International Nuclear Information System (INIS)

Smet, P.F.; Korthout, K.; Haecke, J.E. van; Poelman, D.

2008-01-01

Rare earth doped thiosilicates are promising materials for use in phosphor converted light emitting diodes (pcLEDs). These phosphors (including the hosts Ca 2 SiS 4 , BaSi 2 S 5 and Ba 2 SiS 4 in combination with Ce 3+ and/or Eu 2+ doping) cover the entire visible part of the spectrum, as the emission colour can be changed from deep blue to red. The photoluminescence emission spectrum and the overlap of the excitation spectrum with the emission of pumping LEDs is evaluated. The trade-off between high colour rendering and high electrical-to-optical power efficiency is discussed by simulation with both blue and UV emitting LEDs. Finally, a phosphor combination with low colour temperature (3000 K) and high colour rendering (CRI = 93) is proposed

Color tunability of Sm{sup 3+} doped antimony–phosphate glass phosphors showing broadband fluorescence

Energy Technology Data Exchange (ETDEWEB)

Xiao, P. [School of Textile and Material Engineering, Dalian Polytechnic University, Dalian 116034 (China); Zhang, J.J., E-mail: zhangjj@dlpu.edu.cn [School of Textile and Material Engineering, Dalian Polytechnic University, Dalian 116034 (China); Shen, L.F. [Department of Electronic Engineering and State Key Laboratory of Millimeter Waves, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (China); Wang, Z.Q. [School of Textile and Material Engineering, Dalian Polytechnic University, Dalian 116034 (China); Pun, E.Y.B. [Department of Electronic Engineering and State Key Laboratory of Millimeter Waves, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (China); Lin, H., E-mail: lhai8686@yahoo.com [School of Textile and Material Engineering, Dalian Polytechnic University, Dalian 116034 (China); Department of Electronic Engineering and State Key Laboratory of Millimeter Waves, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (China)

2016-10-15

Sm{sup 3+} doped multicomponent antimony phosphate (MSP) luminescent glasses were prepared and tunable white fluorescence has been investigated. Broad visible emission depending on excitation wavelength is validated to be dominated by discrepant Sb{sup 3+} emitting centers. Group of narrow emissions from Sm{sup 3+} is beneficial to adding yellow and red components in Sm{sup 3+} doped MSP glasses, which is strengthened by effective energy transfer from Sb{sup 3+} to Sm{sup 3+}. Excitation wavelength selection and Sm{sup 3+} concentration adjustment are two feasible routes to optimize luminescence color in Sm{sup 3+} doped MSP glasses and the color tunability of fluorescence indicates that amorphous Sm{sup 3+} doped MSP glass phosphors possess potential for ideal white light devices.

Thermoluminescence glow curve analysis and CGCD method for erbium doped CaZrO{sub 3} phosphor

Energy Technology Data Exchange (ETDEWEB)

Tiwari, Ratnesh, E-mail: 31rati@gmail.com [Department of Physics, Bhilai Institute of Technology, Raipur, 493661 (India); Chopra, Seema [Department Physics, G.D Goenka Public School (India)

2016-05-06

The manuscript report the synthesis, thermoluminescence study at fixed concentration of Er{sup 3+} (1 mol%) doped CaZrO{sub 3} phosphor. The phosphors were prepared by modified solid state reaction method. The powder sample was characterized by thermoluminescence (TL) glow curve analysis. In TL glow curve the optimized concentration in 1mol% for UV irradiated sample. The kinetic parameters were calculated by computerized glow curve deconvolution (CGCD) techniaue. Trapping parameters gives the information of dosimetry loss in prepared phosphor and its usability in environmental monitoring and for personal monitoring. CGCD is the advance tool for analysis of complicated TL glow curves.

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)

Thermoluminescence studies of natural and doped calcium fluoride phosphors

International Nuclear Information System (INIS)

El Kolaly, M.A.

1977-01-01

The various aspects of thermoluminescence (TL) of calcium fluoride phosphors obtained both from natural and laboratory-grown CaF 2 crystals have been investigated in the temperature range from room temperature to 750 deg C. Dopants used in these studies were Mn, Y and lanthanide series rare earths. The aspects which have been investigated are : (1) effect of single and double doping on TL glow curves and TL emission spectra after gamma irradiation, (2) TL traps : their kinetics including evaluation of the activation energy using different techniques, their decay kinetics and their behaviour under partially filled conditions, and (3) effect of temperature on emission of intensity of X-ray induced luminescence and TL. During the course of these investigations, a new glow peak was observed at 650 deg C in natural CaF 2 . It was found that this peak could also be produced in synthetic CaF 2 doped with (Y + Sm). A new model for the TL trap has also been proposed. (M.G.B.)

An investigation on photoluminescence and energy transfer of Eu{sup 3+}/Sm{sup 3+} single-doped and co-doped Ca{sub 4}YO(BO{sub 3}){sub 3} phosphors

Energy Technology Data Exchange (ETDEWEB)

Bandi, Vengala Rao; Grandhe, Bhaskar Kumar [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jang, Kiwan, E-mail: kwjang@changwon.ac.kr [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Shin, Dong-Soo [Department of Chemistry, Changwon National University, Changwon (Korea, Republic of); Yi, Soung-Soo [Department of Photonics, Silla University, Busan (Korea, Republic of); Jeong, Jung-Hyun [Department of Physics, Pukyong National University, Busan (Korea, Republic of)

2013-07-15

The present investigation aims to demonstrate the potentiality of Eu{sup 3+}/Sm{sup 3+} single-doped and co-doped Ca{sub 4}YO(BO{sub 3}){sub 3} phosphors, which were prepared by a sol–gel method. The X-ray diffraction (XRD) profiles showed that all the observed peaks could be attributed to the monoclinic phase of Ca{sub 4}YO(BO{sub 3}){sub 3}. From the measured emission profiles, we have noticed that both the single-doped Eu{sup 3+}/Sm{sup 3+} phosphors shows four emission transitions of {sup 5}D{sub 0} → {sup 7}F{sub 0,1,2,3} and {sup 4}G{sub 5/2} → {sup 6}H{sub 5/2,7/2,9/2,11/2} respectively. Among them, the {sup 5}D{sub 0} → {sup 7}F{sub 2} of Eu{sup 3+} and {sup 4}G{sub 5/2} → {sup 6}H{sub 7/2} of Sm{sup 3+} are intense emission transitions, leading to an intense red color emission from the prepared phosphors. The excitation spectra showed that Eu{sup 3+}/Sm{sup 3+} doped samples can be excited efficiently by 394 nm and 402 nm respectively, incidentally which matches well with the characteristic emission from UVLED. The co-doping of Sm{sup 3+} ions can broaden and strengthen the absorption of near UV region and to be efficient to sensitize the emission of the Ca{sub 4}YO(BO{sub 3}){sub 3}:Eu{sup 3+} phosphor. The mechanism involved in the energy transfer between Eu{sup 3+} and Sm{sup 3+} has been explained and elucidated by an energy level diagram. - Highlights: • Eu{sup 3+} or/and Sm{sup 3+}:Ca{sub 4}YO(BO{sub 3}){sub 3} phosphors were prepared by sol–gel method. • The co-doping of Sm{sup 3+} to Ca{sub 4}YO(BO{sub 3}){sub 3}:Eu{sup 3+} extends its absorption of NUV region. • It has intense absorption in NUV region, which is suitable for NUV LED. • The energy transfer process between Eu{sup 3+} and Sm{sup 3+} ions were discussed.

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).

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).

Photoluminescence study of Dy3+ doped SrCeVO5 phosphor

International Nuclear Information System (INIS)

Suresh, K.; Dai, Ch. Vijay Anil; Murthy, K.V.R.

2016-01-01

Dy 3+ doped SrCeVO 5 phosphor was synthesized by the solid-state reaction method. Photoluminescence (PL) technique was performed to characterize the sample. The excitation spectra monitored under 520 nm and 610 nm wavelength was characterized by a broad band ranging from 220-400 nm. From the excitation spectra two main bands at 265 nm and 325 nm were observed. The PLE intensity of 520 nm monitored shows high intensity than 610 nm spectrum. The emission spectra of SrCeVO 5 phosphor under excitations at 265 nm and 325 nm exhibited main peak at 515 nm (cyan) which is a strong, intense well resolved peak with FWHM (full width at half maximum) of 130 nm is observed. This emission is mainly may be due to Ce ion but not Dy ion. The same emission under 640 and 670 nm excitations (up conversion) with good intensity was also observed. Commission international de l'eclairage (CIE) co-ordinates under these excitations revealed that this phosphor emit cyan colour and could be used for the generation of white light in display and lamp devices. (author)

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...

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)

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

Thermoluminescence glow curve of CaZrO3 phosphor doped with Eu3+

International Nuclear Information System (INIS)

Tiwari, Neha; Kuraria, R.K.; Kuraria, S.R.

2014-01-01

Behaviour displayed by thermoluminescence analysis of Eu 3+ doped CaZrO 3 phosphor prepared by combustion synthesis technique. The sample was synthesized by combustion method because it is less time taking method as well as low temperature synthesis. For the thermoluminescence study the prepared sample irradiated by UV lamp the wavelength is 254 nm. Every time 2 mg of sample used for TL record at fixed heating rate 5℃ s -1 , sample shows well resolved higher temperature peak at 273℃. The high temperature peak shows more stability and less fading in prepared phosphor which is suitable for TL dosimetry. Also the variation with UV dose (5 to 30 min) shows sublinear response with dose

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

Synthesis and luminescence characterization of Pr3+ doped Sr1.5Ca0.5SiO4 phosphor

Science.gov (United States)

Vidyadharan, Viji; Mani, Kamal P.; Sajna, M. S.; Joseph, Cyriac; Unnikrishnan, N. V.; Biju, P. R.

2014-12-01

Luminescence properties of Pr3+ activated Sr1.5Ca0.5SiO4 phosphors synthesized by solid state reaction method are reported in this work. Blue, orange red and red emissions were observed in the Pr3+ doped sample under 444 nm excitation and these emissions are assigned as 3P0 → 3H4, 3P0 → 3H6 and 3P0 → 3F4 transitions. The emission intensity shows a maximum corresponding to the 0.5 wt% Pr3+ ion. The decay analysis was done for 0.05 and 0.5 wt% Pr3+ doped samples for the transition 3P0 → 3H6. The life times of 0.05 and 0.5 wt% Pr3+ doped samples were calculated by fitting to exponential and non-exponential curve respectively, and are found to be 156 and 105 μs respectively. The non-exponential behaviour arises due to the statistical distribution of the distances between the ground state Pr3+ ions and excited state Pr3+ ions, which cause the inhomogeneous energy transfer rate. The XRD spectrum confirmed the triclinic phase of the prepared phosphors. The compositions of the samples were determined by the energy dispersive X-ray spectra. From the SEM images it is observed that the particles are agglomerated and are irregularly shaped. IR absorption bands were assigned to different vibrational modes. The well resolved peaks shown in the absorption spectra are identical to the excitation spectra of the phosphor samples. Pr3+ activated Sr1.5Ca0.5SiO4 phosphors can be efficiently excited with 444 nm irradiation and emit multicolour visible emissions. From the CIE diagram it can be seen that the prepared phosphor samples give yellowish-green emission.

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

Synthesis and luminescent properties of Sm3+ doped zinc aluminate phosphor

Science.gov (United States)

Mahajan, Rubby; Kumar, Sandeep; Prakash, Ram; Kumar, Vinay

2018-05-01

Zinc Aluminate (ZnAl2O4) is a well-known wide band gap oxide that belongs to a class of mixed-metal oxides knows as spinels (AB2O4) where A and B are divalent and trivalent cations. Herein, the structural and photoluminescence properties of Sm3+ ion doped with ZnAl2O4 phosphors are reported. The nanophosphors were synthesized via solution combustion synthesis route at temperature 570 °C. The synthesized samples were characterized by X-ray powder diffraction (XRD), Photoluminescence (PL) spectroscopy, and Ultraviolet-visible spectroscopy. The XRD pattern confirms the cubic phase of phosphor. The calculated lattice parameter were found as a = b = c = 8.0517Å and V = 521.85Å3. The crystallite size of the phosphor was calculated using the Debye-Scherrer formula and found to be ˜19 nm. The emission spectrum at excitation wavelength of 401 nm gave the emission peaks at 563 nm, 601 nm, 648 nm, 697 nm corresponding to the transitions 4G5/2→ 6H5/2, 4G5/2→6H7/2, 4G5/2→6H9/2, 4G5/2 → 6H11/2 of Sm3+ ions, respectively. The diffuse reflectance spectrum was used to calculate the band gap of material and found to be 5.12 eV. The CIE coordinates were found to be (x = 0.56, y = 0.40) that falls in the orange red region of the color gamut. The present phosphor may have potential applications as phosphor for near UV WLED for solid state lighting.

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.

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

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.

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

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)

Solvothermally synthesized europium-doped CdS nanorods: applications as phosphors

International Nuclear Information System (INIS)

Kumar, Sunil; Jindal, Zinki; Kumari, Nitu; Verma, Narendra Kumar

2011-01-01

To exploit the photoluminescent behavior of CdS at nanoscale with different doping concentration of europium—a rare earth element, we report the synthesis of Eu-doped CdS nanorods by using low temperature solvothermal process by using ethylenediamine. The outcomes can have future applications as phosphors, photovoltaic cells, lasers, light emitting diodes, bio-imaging, and sensors. The doping was confirmed by electron dispersive spectroscopy supported by X-ray diffraction. From scanning electron microscopy and transmission electron microscopy analysis it was observed that the average diameter of the Cd 1−x Eu x S nanorods is about 10–12 nm having lengths in the range of 50–100 nm. UV–Visible spectroscopy study was carried out to determine the band gap of the nanorods and the absorbance peaks showed blue shift with respect to the bulk CdS. The blue shift was also observed as the doping concentration of Eu increases. From photoluminescence (PL) studies at λ ex = 450 nm, peaks at 528 and 540 nm were observed due to CdS, peak at 570 nm is due to defects related transitions, while the peak at 613 nm is due to Eu. As the doping concentration of Eu is increased the intensity of the luminescent peak at 613 nm is increased. Thermogravimetric analysis showed the nanorods are thermally stable up to 300 °C. The traces of impurities adsorbed on the nanorods were confirmed by Fourier transform infrared spectroscopy.

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.

Host sensitized near-infrared emission in Nd3+ doped different alkaline-sodium-phosphate phosphors

Science.gov (United States)

Balakrishna, A.; Swart, H. C.; Kroon, R. E.; Ntwaeaborwa, O. M.

2018-04-01

Near-infrared (NIR) emitting phosphors of different alkaline based sodium-phosphate (MNa[PO4], where M = Mg, Ca, Sr and Ba were prepared by a conventional solution combustion method with fixed doping concentration of Nd3+ (1.0 mol%). The phosphors were characterized by powder X-ray diffraction, field emission scanning electron microscope, Fourier transform infrared spectroscopy, UV-vis spectroscopy and fluorescent spectrophotometry. The optical properties including reflectance, excitation and emission were investigated. The excitation spectra of the phosphors were characterized by a broadband extending from 450 to 900 nm. Upon excitation with a wavelength of 580 nm, the phosphor emits intensely infrared region at 872 nm, 1060 nm and 1325 nm which correspond to the 4F3/2 → 4I9/2, 4F3/2 → 4I11/2 and 4F3/2 → 4I13/2 transitions of Nd3+ ions and were found to vary for the different hosts. The strongest emission wavelength reaches 1060 nm. The most intense emission of Nd3+ was observed from Ca2+ incorporated host. The down conversion emissions of the material fall in the NIR region suggesting that the prepared phosphors have potential application in the development of photonic devices emitting in the NIR.

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

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)

Synthesis and thermoluminescence behavior of ZrO2:Eu3+ with variable concentration of Eu3+ doped phosphor

Directory of Open Access Journals (Sweden)

Raunak Kumar Tamrakar

2014-10-01

Full Text Available Cubical ZrO2 phosphor doped with the europium synthesized by conventional solid state synthesis method. The prepared phosphor was characterized by X-ray diffraction (XRD technique, field emission gun scanning electron microscopy (FEGSEM and transmission electron microscopy (TEM. In this paper, we focused on the thermoluminescence glow curves and kinetic parameters, activation energy, order of kinetics, and the frequency factor of ZrO2:Eu3+ phosphor under different doses of UV irradiations at a heating rate of 6.7 °C/s. The kinetic parameters activation energy E, the order of kinetics b, and the frequency factor s of synthesized phosphor of ZrO2:Eu3+ have been calculated by using a peak shape method.

Luminescence properties of dysprosium doped calcium magnesium silicate phosphor by solid state reaction method

Energy Technology Data Exchange (ETDEWEB)

Sahu, Ishwar Prasad, E-mail: ishwarprasad1986@gmail.com [School of Studies in Physics & Astrophysics, Pt. Ravishankar Shukla University, Raipur, C.G. 492010 (India); Chandrakar, Priya; Baghel, R.N.; Bisen, D.P.; Brahme, Nameeta [School of Studies in Physics & Astrophysics, Pt. Ravishankar Shukla University, Raipur, C.G. 492010 (India); Tamrakar, Raunak Kumar [Department of Applied Physics, Bhilai Institute of Technology, Durg, C.G. 491001 (India)

2015-11-15

Dysprosium doped calcium magnesium silicate (CaMgSi{sub 2}O{sub 6}:Dy{sup 3+}) white light emitting phosphor was synthesized by solid state reaction process. The crystal structure of sintered phosphor was monoclinic structure with space group C2/c. Chemical composition of the sintered CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor was confirmed by EDX. The prepared CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor was excited from 352 nm and their corresponding emission spectra were recorded at blue (470 nm), yellow (570 nm) and red (675 nm) line due to the {sup 4}F{sub 9/2} → {sup 6}H{sub 15/2}, {sup 4}F{sub 9/2} → {sup 6}H{sub 13/2}, {sup 4}F{sub 9/2} → {sup 6}H{sub 11/2} transitions of Dy{sup 3+} ions. The combination of these three emissions constituted as white light confirmed by the Commission Internationale de L'Eclairage (CIE) chromatic coordinate diagram. The possible mechanism of the white light emitting long lasting CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor was also investigated. Investigation on afterglow property show that phosphor held fast and slow decay process. The peak of mechanoluminescence (ML) intensity increases linearly with increasing impact velocity of the moving piston. Thus the present investigation indicates that the local piezoelectricity-induced electron bombardment model is responsible to produce ML in prepared CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor. - Highlights: • The crystal structure of CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor is consistent with standard monoclinic structure. • CIE coordinates of CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor is suitable as white light emitting phosphor. • The local piezoelectricity-induced electron bombardment model is responsible to produce ML in CaMgSi{sub 2}O{sub 6}:Dy{sup 3+} phosphor.

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...

Radioluminescence of red-emitting Eu-doped phosphors for fiberoptic dosimetry

Energy Technology Data Exchange (ETDEWEB)

Molina, P.; Santiago, M.; Marcazzo, J.; Caselli, E. [Universidad Nacional del Centro de la Provincia de Buenos Aires, Instituto de Fisica Arroyo Seco, Pinto 399, 7000 Tandil (Argentina); Spano, F. [Autoridad Regulatoria Nuclear, Av. del Libertador 8250, 1429 Buenos Aires (Argentina); Henniger, J. [Institut fur Kern-und Teilchenphysik, Zellescher Weg 19, 01069 Dresden (Germany); Cravero, W., E-mail: pmolina@exa.unicen.edu.ar [Universidad Nacional del Sur, Departamento de Fisica, Av. Colon 80, 8000FTN Bahia Blanca, Buenos Aires (Argentina)

2011-10-15

The fiberoptic dosimetry technique (FOD) has become an attractive method for in-vivo real-time dosimetry in radiotherapy. It is based on the use of a tiny piece of scintillator coupled to the end of an optical fiber, which collects the light emitted by the scintillator during irradiation (radioluminescence). Carbon-doped aluminum oxide (Al{sub 2}O{sub 3}:C) is one of the most radioluminescence materials for FOD due to its high efficiency but it presents the drawback of emitting in the spectral region, where spurious luminescence is also important. Spurious luminescence from optical fiber, termed stem effect, is the main problem afflicting FOD. Several techniques have been applied to remove the stem effect. Optical filtering, which consists in using long-pass filters, is the simplest one. This technique is useful when red-emitting scintillators are employed. In this work, the feasibility of using red-emitting Eu-doped phosphors as FOD scintillators has been investigated. (Author)

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)

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

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

Structural and optical analysis on europium doped AZrO{sub 3} (A=Ba, Ca, Sr) phosphor for display devices application

Energy Technology Data Exchange (ETDEWEB)

Dubey, Vikas, E-mail: jsvikasdubey@gmail.com [Department of Physics, Bhilai Institute of Technology Raipur, 493661 (India); Tiwari, Neha [Department of Physics, Govt. Model Science College, Jabalpur (India)

2016-05-06

Behavior displayed by europium doped AZrO{sub 3} phosphor which was synthesized by solid state reaction method. For synthesis of BaZrO{sub 3}, SrZrO{sub 3} and CaZrO{sub 3} phosphor with fixed concentration of europium ion was calcination at 1000°C and sintered at 1300°C following intermediate grinding. Synthesized sample was characterized by X-ray diffraction analysis and crystallite sized was calculated by Scherer’s formula. From PL spectra of prepared phosphors shows intense emission centred at 612nm (red emission) with high intensity for SrZrO{sub 3}:Eu{sup 3+}. For europium doped BaZrO{sub 3} and CaZrO{sub 3} (613nm) phosphor shows less intense PL spectra as compared to SrZrO{sub 3}:Eu{sup 3+}. The strong emission peak of AZrO{sub 3}:Eu{sup 3+} phosphor is due to forced electric dipole transition of {sup 5}D{sub 0} to {sup 7}F{sub 2} centered at 612 and 613nm. It is characteristic red emission for europium ion. The excitation spectra of AZrO{sub 3}:Eu{sup 3+} phosphor mainly consists of the charge transfer and (CTB) of Eu{sup 3+} located in 200–350 nm centred at 254nm. The present phosphors can act as single host for red light emission in display devices. The CIE coordinates were calculated by Spectrophotometric method using the spectral energy distribution of the AZrO{sub 3}:Eu{sup 3+} sample.

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)

Considerable photoluminescence enhancement of LiEu(MoO4)2 red phosphors via Bi and/or Si doping for white LEDs

International Nuclear Information System (INIS)

Wang, Qing-Feng; Liu, Ying; Wang, Yu; Wang, Wenxi; Wan, Yi; Wang, Gui-Gen; Lu, Zhou-Guang

2015-01-01

Graphical abstract: Doping of Bi and Si into the lattice leads to an considerable increase of the excitation efficiency and luminous intensity, and obvious movement of the CIE chromaticity coordinates to the NTSC standard values of the LiEu(MoO 4 ) 2 , a promising red phosphors suitable for near UV excited white-light emitting diodes. - Highlights: • High performance red phosphors for near UV light excited white LEDs. • Lithium lanthanide molybdate red phosphors. • Bi and Si substitution. • Considerable enhancement of luminescence intensity and excitation efficiency. • CIE chromaticity coordinates very close to the NTSC standard values. - Abstract: Novel Bi and/or Si substituted LiEu(MoO 4 ) 2 phosphors, where Bi was used as sensitizer to enhance the emission intensity and Si was used as substitution to improve the excitation efficiency, were prepared using the sol–gel method, and the photoluminescent properties of the resulting phosphors were intensively investigated. All samples can be excited efficiently by UV (395 nm) light and emit bright red light at 614 nm, which are coupled well with the characteristic emission from a UV-LED. In the Bi 3+ -doped samples, the intensities of the main emission line ( 5 D 0 – 7 F 2 transition at 614 nm) are strengthened because of the energy transition from Bi 3+ to Eu 3+ . With the substitution of Mo 4+ by Si 4+ , there are no significant changes in the emission peak positions, but the emission intensity was significantly enhanced under 395 nm excitation. Particularly, the LiEu 0.9 Bi 0.1 (Mo 0.97 Si 0.03 O 4 ) 2 phosphor doped with both Bi and Si demonstrates superior comprehensive photoluminescence properties with an excellent combination of easy excitation in the near UV range, bright emission intensity, high PL quantum efficiency as well as suitable decay time, which are very suitable for application as red phosphor for near UV type LEDs

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.

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

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

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)

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

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.

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

Luminescence properties of Y2O3:Bi3+, Yb3+ co-doped phosphor for application in solar cells

Science.gov (United States)

Lee, E.; Kroon, R. E.; Terblans, J. J.; Swart, H. C.

2018-04-01

Bismuth (Bi3+) and ytterbium (Yb3+) co-doped yttrium oxide (Y2O3) phosphor powder was successfully synthesised using the co-precipitation technique. The X-ray diffraction (XRD) patterns confirmed that a single phase cubic structure with a Ia-3 space group was formed. The visible emission confirmed the two symmetry sites, C2 and S6, found in the Y2O3 host material and revealed that Bi3+ ions preferred the S6 site as seen the stronger emission intensity. The near-infrared (NIR) emission of Yb3+ increased significantly by the presence of the Bi3+ ions when compared to the singly doped Y2O3:Yb3+ phosphor with the same Yb3+ concentration. An increase in the NIR emission intensity was also observed by simply increasing the Yb3+ concentration in the Y2O3:Bi3+, Yb3+ phosphor material where the intensity increased up to x = 5.0 mol% of Yb3+ before decreasing due to concentration quenching.

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...

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

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.)

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)

Doping efficiency analysis of highly phosphorous doped epitaxial/amorphous silicon emitters grown by PECVD for high efficiency silicon solar cells

Energy Technology Data Exchange (ETDEWEB)

El-Gohary, H.G.; Sivoththaman, S. [Waterloo Univ., ON (Canada). Dept. of Electrical and Computer Engineering

2008-08-15

The efficient doping of hydrogenated amorphous and crystalline silicon thin films is a key factor in the fabrication of silicon solar cells. The most popular method for developing those films is plasma enhanced chemical vapor deposition (PECVD) because it minimizes defect density and improves doping efficiency. This paper discussed the preparation of different structure phosphorous doped silicon emitters ranging from epitaxial to amorphous films at low temperature. Phosphine (PH{sub 3}) was employed as the doping gas source with the same gas concentration for both epitaxial and amorphous silicon emitters. The paper presented an analysis of dopant activation by applying a very short rapid thermal annealing process (RTP). A spreading resistance profile (SRP) and SIMS analysis were used to detect both the active dopant and the dopant concentrations, respectively. The paper also provided the results of a structural analysis for both bulk and cross-section at the interface using high-resolution transmission electron microscopy and Raman spectroscopy, for epitaxial and amorphous films. It was concluded that a unity doping efficiency could be achieved in epitaxial layers by applying an optimized temperature profile using short time processing rapid thermal processing technique. The high quality, one step epitaxial layers, led to both high conductive and high doping efficiency layers.

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.

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.

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.

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.

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

Synthesis and photoluminescence properties of Pb{sup 2+} doped inorganic borate phosphor NaSr{sub 4}(BO{sub 3}){sub 3}

Energy Technology Data Exchange (ETDEWEB)

Chauhan, A. O., E-mail: abhi2718@gmail.com; Koparkar, K. A.; Omanwar, S. K. [Department of Physics, SantGadge Baba Amravati University, Amravati MH, 444602 (India); Bajaj, N. S. [Department of Physics, Toshniwal Art, Commerce and Science College, Sengoan, Hingoli MH (India)

2016-05-06

A series of Inorganic borate phosphors NaSr{sub 4}(BO{sub 3}){sub 3} doped with Pb{sup 2+} was successfully synthesized by modified solid state diffusion method. The crystal structure and the phase purity of sample were characterized by powder X-ray diffraction (XRD). The photoluminescence properties of synthesized materials were investigated using spectrofluorometer at room temperature. The phosphor show strong broad band emission spectra in UVA region maximum at 370 nm under the excitation of 289 nm. The dependence of the emission intensity on the Pb{sup 2+} concentration for the NaSr{sub 4}(BO{sub 3}){sub 3} were studied in details. The concentration quenching of Pb{sup 2+} doped NaSr{sub 4}(BO{sub 3}){sub 3} was observed at 0.02 mol. The Stokes shifts of NaSr{sub 4}(BO{sub 3}){sub 3}: Pb{sup 2+} phosphor was calculated to be 7574 cm{sup −1}.

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

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.

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

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. %

Effect of Thermal Annealing on Carbon in In-situ Phosphorous-Doped Si1-xCx films

International Nuclear Information System (INIS)

Adam, Thomas; Loubet, Nicolas; Reznicek, Alexander; Paruchuri, Vamsi; Sampson, Ron; Sadana, Devendra

2012-01-01

The effect of thermal heat treatment on carbon in in-situ phosphorous-doped silicon-carbon is studied as a function of annealing temperature and type. Films of 0 to 2% carbon were deposited using cyclic chemical vapor deposition at reduced pressures. Secondary ion-mass spectroscopy and high-resolution X-ray diffraction were employed to extract the total and substitutional carbon concentration in samples with phosphorous levels of mid-10 20 cm -3 . It was found that millisecond laser annealing drastically improves substitutionality while high thermal budget treatments (furnace, rapid-thermal, or spike annealing) resulted in an almost complete loss of substitutional carbon, independent of preceding or subsequent laser heat treatments.

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.

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

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)

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)

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

A novel red phosphor Mg2GeO4 doped with Eu3+ for PDP applications

International Nuclear Information System (INIS)

Yang Hongmei; Shi Jianxin; Liang Hongbin; Gong Menglian

2006-01-01

A novel red emitting phosphor, Eu 3+ -doped Mg 2 GeO 4 , was prepared by the solid-state reaction. X-ray powder diffraction (XRD) analysis confirmed the formation of Mg 2 GeO 4 :Eu 3+ . Field-emission-scanning electron microscopy (FE-SEM) observation indicated a narrow size-distribution of about 0.5-2 μm nm for the particles with spindle-like shape. Photoluminescence (PL) and vacuum ultraviolet (VUV) excitation characteristics of the phosphor Mg 2 GeO 4 :Eu 3+ were studied. We have also studied the effect of preparation conditions such as temperature, heating time on the PL data. Photoluminescence measurements indicated that the phosphor exhibits bright red emission at about 609 nm under UV excitation. And the vacuum ultraviolet spectra present that the novel red phosphor Mg 2 GeO 4 :Eu 3+ shows strong absorption in the VUV region, which ensures the efficient absorption of the Xe plasma emission lines. The phosphor Mg 2 GeO 4 :Eu 3+ shows the strongest emission at 613 nm corresponding to the electric dipole 5 D - 7 F 2 transition of Eu 3+ excited at 147 nm. The optical properties study suggests that it is a potential candidate for plasma display panels (PDPs) application

Sol–gel synthesis and photoluminescence studies on colour tuneable Dy3+/Tm3+ co-doped NaGd(WO4)2 phosphor for white light emission

International Nuclear Information System (INIS)

Durairajan, A.; Balaji, D.; Rasu, K. Kavi; Moorthy Babu, S.; Hayakawa, Y.; Valente, M.A.

2015-01-01

A series of Dy 3+ /Tm 3+ ion co-doped NaGd(WO 4 ) 2 (NGW) phosphors were synthesised by a sol–gel method at low temperature for white light emission. The structural and luminescence properties of the synthesised phosphors were studied by powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), Raman and photoluminescence techniques. In Dy 3+ /Tm 3+ :NGW phosphors, the dopant ions substituted Gd 3+ ions that are located in S 4 sites of NGW host lattice. In NGW host, under UV excitation the Dy 3+ ions have shown strong yellow ( 4 F 9/2 → 6 H 13/2 ) and comparatively weak blue ( 4 F 9/2 → 6 H 15/2 ) emission transitions at 575 and 488 nm, respectively. Due to deficient blue colour the overall emission falls in yellow region. Hence, Tm 3+ ions having strong blue emission at 455 nm corresponding to the transition 1 D 2 → 3 F 4 were co-activated along with Dy 3+ ions in NGW matrix. By changing the doping concentrations of Tm 3+ and Dy 3+ ions in NGW, white light emission was tuned by 353 nm excitation wavelength. Their corresponding colour co-ordinates were calculated and found to be very close to the white colour chromaticity co-ordinates (0.333, 0.333). - Highlights: • Dy 3+ and Dy 3+ /Tm 3+ :NGW phosphors were synthesised by sol–gel methods. • The excitation spectrum confirmed the strong absorption in near-UV region. • The emission spectrum shows the yellow and white emission to doped and co-doped phosphors respectively. • The CIE co-ordinate conforms close to daylight emission

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

Long-wave UVA radiation excited warm white-light emitting NaGdTiO4: Tm3+/Dy3+/Eu3+ ions tri-doped phosphors: Synthesis, energy transfer and color tunable properties

International Nuclear Information System (INIS)

Bharat, L. Krishna; Du, Peng; Yu, Jae Su

2016-01-01

NaGdTiO 4 (NGT) phosphors doped with different activator ions (Tm 3+ , Dy 3+ , and Eu 3+ ) were synthesized by a conventional solid-state reaction method in an ambient atmosphere. These phosphors were characterized by scanning electron microscope images, transmission electron microscope images, X-ray diffraction patterns, Fourier transform infrared spectra, and photoluminescence spectra. All the samples were crystallized in an orthorhombic phase with a space group of Pbcm (57). In Tm 3+ /Dy 3+ ions co-doped samples, white-light emission was observed under near-ultraviolet (NUV) excitation. In addition, the energy transfer between Tm 3+ and Dy 3+ ions was proved to be a resonant type via an electric dipole–dipole mechanism and the critical distance of energy transfer was calculated to be 19.91 Å. Furthermore, Tm 3+ /Dy 3+ /Eu 3+ ions tri-doped NGT phosphors demonstrated warm white-light emission by appropriately tuning the activator content, based on the principle of energy transfer. These NUV wavelength excitable phosphors exhibit great potential as a single-phase full-color emitting phosphor for white light-emitting diode applications. - Highlights: • The pebble shaped NaGdTiO 4 particles were prepared by solid-state reaction method. • Tm 3+ and Dy 3+ single doping gives respective blue and cool white light emission. • The Tm 3+ /Dy 3+ ions co-doped samples give CIE values near to standard white light. • Addition of Eu 3+ ions shifts the CIE values towards warm white light region. • This single phase white light emitting phosphors have lower CCT values (<5000 K).

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)

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

The synthesis and luminescence properties of a novel red-emitting phosphor: Eu3+-doped Ca9La(PO4)7

Science.gov (United States)

Liang, Zehui; Mu, Zhongfei; Wang, Qiang; Zhu, Daoyun; Wu, Fugen

2017-10-01

A series of novel red-emitting phosphors Ca9La1- x (PO4)7: xEu3+ were synthesized by high-temperature solid state reactions. The photoluminescence excitation and photoluminescence spectra of these phosphors were investigated in detail. O2--Eu3+ charge transfer band peaking at about 261 nm is dominant in the PLE spectra of Eu3+-doped Ca9La(PO4)7, indicating that the phosphors are suitable for tricolor fluorescent lamps. The phosphors also show a good absorption in near ultraviolet (around 395 nm) and blue (around 465 nm) spectral region, which indicates that it can be pumped with NUV and blue chips for white light-emitting diodes. The transition of 5D0 → 7F2 of Eu3+ in this lattice can emit bright red light. Ca9La(PO4)7 could accommodate a large amount of Eu3+ with an optimal concentration of 60 mol%. The dipole-dipole interaction between Eu3+ is the dominant mechanism for concentration quenching of Eu3+. The calculated color coordinates lie in red region ( x = 0.64, y = 0.36), which is close to Y2O3: 0.05Eu3+ ( x = 0.65, y = 0.34). The integral emission intensity of Ca9La0.4(PO4)7: 0.6Eu3+ is 1.9 times stronger than that of widely used commercial red phosphor Y2O3: 0.05Eu3+. All these results indicate that Eu3+-doped Ca9La(PO4)7 is a promising red-emitting phosphor which can be used in tricolor fluorescent lamps and white light-emitting diodes.

Considerable photoluminescence enhancement of LiEu(MoO{sub 4}){sub 2} red phosphors via Bi and/or Si doping for white LEDs

Energy Technology Data Exchange (ETDEWEB)

Wang, Qing-Feng [Department of Materials Science and Engineering, Harbin Institute of Technology Shenzhen Graduate School, Shenzhen, Guangdong 518055 (China); Department of Materials Science and Engineering, South University of Science and Technology of China, Shenzhen, Guangdong 518055 (China); Liu, Ying [Department of Materials Science and Engineering, South University of Science and Technology of China, Shenzhen, Guangdong 518055 (China); Wang, Yu [Department of Physics and Materials Science, City University of Hong Kong, Hong Kong Special Administrative Region (Hong Kong); Wang, Wenxi; Wan, Yi [Department of Materials Science and Engineering, South University of Science and Technology of China, Shenzhen, Guangdong 518055 (China); Wang, Gui-Gen [Department of Materials Science and Engineering, Harbin Institute of Technology Shenzhen Graduate School, Shenzhen, Guangdong 518055 (China); Lu, Zhou-Guang [Department of Materials Science and Engineering, South University of Science and Technology of China, Shenzhen, Guangdong 518055 (China)

2015-03-15

Graphical abstract: Doping of Bi and Si into the lattice leads to an considerable increase of the excitation efficiency and luminous intensity, and obvious movement of the CIE chromaticity coordinates to the NTSC standard values of the LiEu(MoO{sub 4}){sub 2}, a promising red phosphors suitable for near UV excited white-light emitting diodes. - Highlights: • High performance red phosphors for near UV light excited white LEDs. • Lithium lanthanide molybdate red phosphors. • Bi and Si substitution. • Considerable enhancement of luminescence intensity and excitation efficiency. • CIE chromaticity coordinates very close to the NTSC standard values. - Abstract: Novel Bi and/or Si substituted LiEu(MoO{sub 4}){sub 2} phosphors, where Bi was used as sensitizer to enhance the emission intensity and Si was used as substitution to improve the excitation efficiency, were prepared using the sol–gel method, and the photoluminescent properties of the resulting phosphors were intensively investigated. All samples can be excited efficiently by UV (395 nm) light and emit bright red light at 614 nm, which are coupled well with the characteristic emission from a UV-LED. In the Bi{sup 3+}-doped samples, the intensities of the main emission line ({sup 5}D{sub 0}–{sup 7}F{sub 2} transition at 614 nm) are strengthened because of the energy transition from Bi{sup 3+} to Eu{sup 3+}. With the substitution of Mo{sup 4+} by Si{sup 4+}, there are no significant changes in the emission peak positions, but the emission intensity was significantly enhanced under 395 nm excitation. Particularly, the LiEu{sub 0.9}Bi{sub 0.1}(Mo{sub 0.97}Si{sub 0.03}O{sub 4}){sub 2} phosphor doped with both Bi and Si demonstrates superior comprehensive photoluminescence properties with an excellent combination of easy excitation in the near UV range, bright emission intensity, high PL quantum efficiency as well as suitable decay time, which are very suitable for application as red phosphor for near UV

Synthesis and effect of Ce and Mn co-doping on photoluminescence characteristics of Ca6AlP5O20:Eu novel phosphors.

Science.gov (United States)

Shinde, K N; Dhoble, S J

2013-01-01

A series of Ca6AlP5O20 doped with rare earths (Eu and Ce) and co-doped (Eu, Ce and Eu,Mn) were prepared by combustion synthesis. Under Hg-free excitation, Ca6AlP5O20:Eu exhibited Eu(2+) (486 nm) emission in the blue region of the spectrum and under near Hg excitation (245 nm), Ca6AlP5O20:Ce phosphor exhibited Ce(3+) emission (357 nm) in the UV range. Photoluminescence (PL) peak intensity increased in Ca6AlP5O20:Eu,Ce and Ca6AlP5O20:Eu, Mn phosphors due to co-activators of Ce(3+) and Mn(2+) ions. As a result, these ions played an important role in PL emission in the present matrix. Ca6AlP5O20:Eu, Ce and Ca6AlP5O20:Eu, Mn phosphors provided energy transfer mechanisms via Ce(3+) → Eu(2+) and Eu(2+) → Mn(2+), respectively. Eu ions acted as activators and Ce ions acted as sensitizers. Ce emission energy was well matched with Eu excitation energy in the case of Ca6AlP5O20:Eu, Ce and Eu ions acted as activators and Mn ions acted as sensitizers in Ca6AlP5O20:Eu, Mn. This study included synthesis of new and efficient phosphate phosphors. The impact of doping and co-doping on photoluminescence properties and energy transfer mechanisms were investigated and we propose a feasible interpretation. Copyright © 2012 John Wiley & Sons, Ltd.

Effect of killer impurities on laser-excited barium-doped ZnS phosphors at liquid nitrogen temperature

Science.gov (United States)

Kumar, Sunil; Verma, N. K.; Bhatti, H. S.

Zinc sulphide phosphors doped with Ba, as well as killer impurities of Fe, Co and Ni, having variable concentrations, were synthesized; and using an ultraviolet laser as the excitation source, decay-curve analyses were done. Various strong emissions in these phosphors were detected and the corresponding excited-state life times were measured at liquid nitrogen temperature. Studies were carried out to see the effect of killer impurities on the phosphorescence excited-state life times. Excited-state life times were found to decrease appreciably (microsecond to nanosecond) with the addition of quenchers. These studies are quite useful and find applications in areas such as optical memories, sensors, luminescent screens, laser-beam detection and alignment, color displays, printing, etc.

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

Trivalent europium-doped strontium molybdate red phosphors in white light-emitting diodes: Synthesis, photophysical properties and theoretical calculations

International Nuclear Information System (INIS)

Yang, W.-Q.; Liu, H.-G.; Liu, G.-K.; Lin, Y.; Gao, M.; Zhao, X.-Y.; Zheng, W.-C.; Chen, Y.; Xu, J.; Li, L.-Z.

2012-01-01

Eu 3+ -doped strontium molybdate red phosphors (Sr 1−x MoO 4 :Eu x (x = 0.01–0.2)) for white light-emitting diodes (LED) were synthesized by the solid-state reaction method. The fluorescent intensities of the as-prepared phosphors were remarkably improved. The excitation and emission spectra demonstrate that these phosphors can be effectively excited by the near-UV light (395 nm) and blue light (466 nm). Their emitted red light peaks are located at 613 nm, and the highest quantum yield value (η) of the as-grown red phosphor, which is 95.85%, is much higher than that of commercial red phosphor (77.53%). These red phosphors plus commercial yellow powers (1:10) were successfully packaged with the GaN-based blue chips on a piranha frame by epoxy resins. The encapsulated white LED lamps show high performance of the CIE chromaticity coordinates and color temperatures. Moreover, to explain the fluorescent spectra of these phosphors, a complete 3003 × 3003 energy matrix was successfully built by an effective operator Hamiltonian including free ion and crystal field interactions. For the first time, the fluorescent spectra for Eu 3+ ion at the tetragonal (S 4 ) Sr 2+ site of SrMoO 4 crystal were calculated from a complete diagonalization (of energy matrix) method. The fitting values are close to the experimental results.

Eu2+-doped OH− free calcium aluminosilicate glass: A phosphor for smart lighting

International Nuclear Information System (INIS)

Lima, S.M.; Andrade, L.H.C.; Rocha, A.C.P.; Silva, J.R.; Farias, A.M.; Medina, A.N.; Baesso, M.L.; Nunes, L.A.O.; Guyot, Y.; Boulon, G.

2013-01-01

In this paper, a broad emission band from Eu 2+ -doped OH − free calcium aluminosilicate glass is reported. By changing the excitation wavelengths, the results showed it is possible to tune the emission from green to orange, what combined with the scattered light from the same blue LED used for excitation, provided a color rendering index of 71 and a correlated color temperature of 6550 K. Our preliminary tests indicate this material as a promising phosphor towards the development of smart lighting devices. -- Highlights: • We report a broad emission band from Eu 2+ -doped OH − free calcium aluminosilicate glass. • The maximum emission peak can be tune from green to orange region. • The test with a LED provided a color rendering index of 71 and a correlated color temperature of 6550 K

The doping sites in Eu2+-doped AIBIIPO4 phosphors and their consequence on the photoluminescence excitation spectra

Science.gov (United States)

Amer, M.; Boutinaud, P.

2018-02-01

The energy corresponding to the excitation edge in Eu2+-doped phosphate phosphors of the type AIBIIPO4 (AI = monovalent cation, BII = divalent cation) is calculated from the knowledge of two crystal-structure-related factors he(X(i)) and Fc(X(i)) which are connected respectively to the crystal field splitting (CFS) and the centroid energy (Ec) of the excited 4f65d1 electron configuration of Eu2+. The calculation is carried out for each cation site X(i) available for Eu2+ in 25 different compositions of AIBIIPO4 including NaZnPO4-Eu2+ for which the luminescence is firstly reported. Our results indicate (1) that is it possible to identify the nature of the cation site that contributes to the excitation edge of Eu2+ in AIBIIPO4 within an accuracy of±1000 cm-1 and (2) that the method can be used as a tool for the predictive design of AIBIIPO4 - Eu2+ phosphors applicable in solid state LED-based lighting.

Rare-earth doped phosphors: oldies or goldies?

International Nuclear Information System (INIS)

Moine, B.; Bizarri, G.

2003-01-01

The scientific research on phosphors has a long history starting more than 100 years ago. But recently the appearance of new kinds of displays and lighting devices (plasma display, fluorescent lamp without mercury, etc.) induced an increase of the research of new phosphors with better luminous efficiency than those available up to now. It has been shown that the behavior of 'classical' phosphors in a plasma display panel is quite different than in a cathode ray tube and that the vacuum ultraviolet (VUV) excitation process has to be studied with care in order to improve the phosphors efficiency. That is particularly true in PDPs. It is well established now that a good phosphor for electronic or ultraviolet excitation is not necessarily a good choice for excitation in VUV. This is probably due to the fact that the excitation process is very different in that case and also because the penetration depth of the VUV photons is extremely small inducing a large contribution of the surface of the phosphor. We will illustrate this with some examples. Methods to accelerate luminous intensity decrease under VUV excitation will be described. Low efficiency, fast aging process are both drawbacks that can be solved only in the framework of fundamental studies. Quantum cutting emission may be a solution for the first one but no satisfactory process was proposed for the moment to solve the second

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

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

Phosphorous-doped TiO2 nanoparticles: synthesis, characterization, and visible photocatalytic evaluation on sulfamethazine degradation.

Science.gov (United States)

Mendiola-Alvarez, Sandra Yadira; Hernández-Ramírez, Ma Aracely; Guzmán-Mar, Jorge Luis; Garza-Tovar, Lorena Leticia; Hinojosa-Reyes, Laura

2018-05-24

Mesoporous phosphorous-doped TiO 2 (TP) with different wt% of P (0.5, 1.0, and 1.5) was synthetized by microwave-assisted sol-gel method. The obtained materials were characterized by XRD with cell parameters refinement approach, Raman, BET-specific surface area analysis, SEM, ICP-OES, UV-Vis with diffuse reflectance, photoluminescence, FTIR, and XPS. The photocatalytic activity under visible light was evaluated on the degradation of sulfamethazine (SMTZ) at pH 8. The characterization of the phosphorous materials (TP) showed that incorporation of P in the lattice of TiO 2 stabilizes the anatase crystalline phase, even increasing the annealing temperature. The mesoporous P-doped materials showed higher surface area and lower average crystallite size, band gap, and particle size; besides, more intense bands attributed to O-H bond were observed by FTIR analysis compared with bare TiO 2 . The P was substitutionally incorporated in the TiO 2 lattice network as P 5+ replacing Ti 4+ to form Ti-O-P bonds and additionally present as PO 4 3-  on the TiO 2 surface. All these characteristics explain the observed superior photocatalytic activity on degradation (100%) and mineralization (32%) of SMTZ under visible radiation by TP catalysts, especially for P-doped TiO 2 1.0 wt% calcined at 450 °C (TP1.0-450). Ammonium, nitrate, and sulfate ions released during the photocatalytic degradation were quantified by ion chromatography; the nitrogen and sulfur mass balance evidenced the partial mineralization of this recalcitrant molecule.

New Silicate Phosphors for a White LED(Electronic Displays)

OpenAIRE

Toda, Kenji; Kawakami, Yoshitaka; Kousaka, Shin-ichiro; Ito, Yutaka; Komeno, Akira; Uematsu, Kazuyoshi; Sato, Mineo

2006-01-01

We focus on the development of new silicate phosphors for a white LED. In the europium doped silicate system, four LED phosphor candidates-Li_2SrSiO_4:Eu^, Ba_9Sc_2Si_6O_:Eu^, Ca_3Si_2O_7:Eu^ and Ba_2MgSi_2O_7:Eu^ were found. Luminescent properties under near UV and visible excitation were investigated for the new Eu^ doped LED silicate phosphors. These new phosphors have a relatively strong absorption band in a long wavelength region.

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.

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 ...

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

Luminescent Enhancement of Na+ and Sm3+ Co-doping Reddish Orange SrCa3Si2O8 Phosphors

Science.gov (United States)

Chun, Fengjun; Zhang, Binbin; Li, Wen; Liu, Honggang; Deng, Wen; Chu, Xiang; Osman, Hanan; Zhang, Haitao; Yang, Weiqing

2018-04-01

Reddish orange SrCa3Si2O8 phosphors, prepared by the facile solid state reaction method, are a luminescent enhancement of Na+ and Sm3+ co-doping luminescent material. Na+ was designed to compensate the charge imbalance of Sm3+ ion substituting for the Sr2+ ion of orthorhombic SrCa3Si2O8 crystals. The results suggest that Na+ can effectively enhance the luminescent intensity of the reddish orange light peaked at about 562 nm (4 G 5/2 → 6 H 5/2), 600 nm (4 G 5/2 → 6 H 7/2) and 645 nm (4 G 5/2 → 6 H 9/2) excited by the near ultraviolet excited light 404 nm (4 L 13/2 → 6 H 5/2). The energy transfer has been further verified by the florescence lifetime. Additionally, the luminescent lifetime τ of as-grown phosphors was separated into two parts, a rapid lifetime and a slow lifetime. The average lifetime results ranged from 2.098 to 1.329 ms which were influenced by the concentration of Sm3+ doping. The systematic researches of as-grown phosphors have clearly suggested a potential application for white-light-emitting diodes ( w-LEDs).

Luminescence characteristics and glow curves analysis of Cu"+ doped Li_3PO_4 phosphor

International Nuclear Information System (INIS)

Aghalte, G.A.; Dhoble, S.J.; Pawar, N.R.

2016-01-01

Li_3PO_4:Cu exhibits useful TL properties in personnel dosimetry of ionizing radiations. Cu is known to be one of the most efficient activator. The PL intensity is found to increase consistently with the increasing quenching temperature. Cu"+ doped Li_3PO_4 phosphor was synthesized by the wet chemical co-precipitation method. The crystal structure and particle morphology of the phosphor was investigated by using X-ray diffraction and scanning electron microscopy. Li_3PO_4:Cu is excellent phosphor for TL dosimetry. For the synthesis of Li_3PO_4:Cu phosphor the stoichiometric amounts of LiOH·H_2O and CuSO_4·"5H_2O were dissolved separately and then the solutions were mixed together. It was precipitated by using concentrated H_3PO_4. The precipitate was filtered out immediately and kept 12 hours below IR lamp. Prepared dry Li_3PO_4:Cu powder was then put on 2.5 wt% NH_4Cl in graphite crucible in preheated furnace at 800°C and was kept for 1 hour. It was then rapidly quenched to room temperature. Thermoluminescence (TL) glow curves were recorded on Nucleonix TL Reader with a heating rate of 2°C per second in the temperature range of 50-250°C. The PMT voltage was 750 volts. Photoluminescence (PL) studies were carried out by Hitachi F-4000 spectrophotometer with a spectral slit width of 1.5 nm

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.

Phosphors doped with Dy3+ and Gd3+ for lighting

International Nuclear Information System (INIS)

Su, Q; Pei, Z.; Zeng, Q.; Chi, L.

1998-01-01

Full text: Some heavy lanthanide ions with even atomic number such as Dy 3+ and Gd 3+ are abundant in the ion adsorption type deposit of China. Their price is cheap and they have specific spectroscopic properties which can be used as phosphors. Dy 3i on has two dominant bands in the emission spectrum. The yellow band (575 nm) corresponds to the hypersensitive transition 4 F 9/2 → 6 H 13/2 (ΔL=2, ΔJ=2), and the blue band (485 nm) corresponds to the 4 F 9/2 → 6 H 15/2 transition. Factors which influence on the yellow- to-blue intensity ratio (Y/B) were investigated. Adjusting to a suitable Y/B, Dy 3+ will emit white light with high colour temperature and can be used for lighting. But Dy 3+ ion has only narrow excitation bands of f-f transitions ranging from 300-500 nm, no broad excitation band such as charge transfer band or f-d transition band exists in the UV region 200-300 nm. Hence its luminescent efficiency is low when it is excited by UV radiation emitted from the mercury plasma. This is one of the drawbacks to its use as lamp phosphor. However, this can be overcome by sensitisation with Gd 3+ , Pb 2+ or other sensitisers such as vanadate shown in this report. Gd 3+ is not only a good matrix, but also a good sensitiser. Using its 8 S 7/2 → 6 D, 6 I and 6 P transitions, the UV excitation energy can be absorbed and transferred to the activator such as Dy 3+ . Therefore, in some cases Gd 3+ is better than Y 3+ which is optical inert as a matrix. For the phosphor Ca 1.96 Pb 0.04 RE 7.9 Dy 0.1 (SiO 4 ) 6 O 2 prepared by sol-gel method, the intensity of Dy 3+ in the Gd 3+ compound (RE=Gd 3+ ) is six times that in the Y 3+ compound. Some new phosphors doped with Dy 3+ and Gd 3+ prepared in our laboratory are reported

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.

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.

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.)

Upconversion emission study of Er3+/Yb3+ doped barium titanate phosphor prepared by co-precipitation method

International Nuclear Information System (INIS)

Mahata, M.K.; Dey, R.; Kumar, K.; Rai, V.K.; Rai, S.B.

2012-01-01

In the present work we have successfully synthesized the Er 3+ , Yb 3+ doped barium titanate phosphor via co-precipitation synthesis method. Under 980 nm excitation, tri-color upconversion fluorescence has been observed. The Fourier Transform Infrared measurement was done to check the presence of organic impurities. In order to find out how many photons are involved in each emission band, the variation of UC emission intensity of the codoped phosphor is studied with increase in excitation power. Upconversion emission spectra show that as the annealing temperature of the powder is increased, intensity of red emission decreases and intensity of green emission increases due to the decrease in maximum phonon frequency of the host material. (author)

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

A novel double perovskite tellurate Eu3+-doped Sr2MgTeO6 red-emitting phosphor with high thermal stability

Science.gov (United States)

Liang, Jingyun; Zhao, Shancang; Yuan, Xuexia; Li, Zengmei

2018-05-01

A series of novel double perovskite tellurate red-emitting phosphors Sr2MgTeO6:xEu3+ (x = 0.05-0.40) were successfully synthesized by a high-temperature solid-state reaction method. The phase structure, photoluminescence properties and thermal stability of the phosphor were investigated in detail. The phosphor shows dominant emission peak at 614 nm belonging to the 5D0 → 7F2 electric dipole transition under 465 nm excitation. The luminescence intensity keeps increasing with increasing the content of Eu3+ to 25 mol%, and the critical transfer distance of Eu3+ was calculated to be 12 Å. The quenching temperature for Sr2MgTeO6:0.25Eu3+ was estimated to be above 500 K. This spectral feature reveals high color purity and excellent chromaticity coordinate characteristics. Therefore, Eu3+-doped Sr2MgTeO6 phosphors are potential red phosphors for blue chip-based white light-emitting diode and display devices.

Tunable photoluminescence and magnetic properties of Dy(3+) and Eu(3+) doped GdVO4 multifunctional phosphors.

Science.gov (United States)

Liu, Yanxia; Liu, Guixia; Dong, Xiangting; Wang, Jinxian; Yu, Wensheng

2015-10-28

A series of Dy(3+) or/and Eu(3+) doped GdVO4 phosphors were successfully prepared by a simple hydrothermal method and characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectrometry (EDS), photoluminescence (PL) spectroscopy and vibrating sample magnetometry (VSM). The results indicate that the as-prepared samples are pure tetragonal phase GdVO4, taking on nanoparticles with an average size of 45 nm. Under ultraviolet (UV) light excitation, the individual Dy(3+) or Eu(3+) ion activated GdVO4 phosphors exhibit excellent emission properties in their respective regions. The mechanism of energy transfer from the VO4(3-) group and the charge transfer band (CTB) to Dy(3+) and Eu(3+) ions is proposed. Color-tunable emissions in GdVO4:Dy(3+),Eu(3+) phosphors are realized through adopting different excitation wavelengths or adjusting the appropriate concentration of Dy(3+) and Eu(3+) when excited by a single excitation wavelength. In addition, the as-prepared samples show paramagnetic properties at room temperature. This kind of multifunctional color-tunable phosphor has great potential applications in the fields of photoelectronic devices and biomedical sciences.

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

Investigation of thermal quenching and abnormal thermal quenching in mixed valence Eu co-doped LaAlO{sub 3} phosphor

Energy Technology Data Exchange (ETDEWEB)

Chen, Jingjing [Tianjin Key Laboratory for Photoelectric Materials and Devices, School of Materials Science and Engineering, Tianjin University of Technology, Tianjin 300384 (China); Zhao, Yang [China academy of civil aviation science and technology, Beijing 100028 (China); Mao, Zhiyong, E-mail: mzhy1984@163.com [Tianjin Key Laboratory for Photoelectric Materials and Devices, School of Materials Science and Engineering, Tianjin University of Technology, Tianjin 300384 (China); Wang, Dajian [Tianjin Key Laboratory for Photoelectric Materials and Devices, School of Materials Science and Engineering, Tianjin University of Technology, Tianjin 300384 (China); Bie, Lijian, E-mail: ljbie@tjut.edu.cn [Tianjin Key Laboratory for Photoelectric Materials and Devices, School of Materials Science and Engineering, Tianjin University of Technology, Tianjin 300384 (China)

2017-06-15

Temperature dependent luminescence of mixed valence Eu co-doped LaAlO{sub 3} phosphors are deeply investigated in this work. Different temperature properties of Eu{sup 2+} and Eu{sup 3+} luminescence are observed as the phosphor excited by different incident light. Eu{sup 3+} luminescence shows normal thermal quenching when excited at 320 nm and abnormal thermal quenching as the excitation light changed into 365 nm, while Eu{sup 2+} luminescence exhibits a normal thermal quenching independent on the incident excitation lights. The origin of these novel normal/abnormal thermal quenching phenomena are analyzed and discussed by the excitation-emission processes in terms of the configuration coordinate model. The presented important experimental and analysis results give insights into the temperature properties of phosphors.

Transition of Emission Colours as a Consequence of Heat-Treatment of Carbon Coated Ce3+-Doped YAG Phosphors

NARCIS (Netherlands)

Yin, L.J.; Dierre, B.F.P.R.; Sekiguchi, Takashi; van Ommen, J.R.; Hintzen, H.T.J.M.; Cho, Yujin

2017-01-01

To modify the luminescence properties of Ce³⁺-doped Y₃Al₅O₁₂ (YAG) phosphors, they have been coated with a carbon layer by chemical vapor deposition and subsequently heat-treated at high temperature under N₂ atmosphere. Luminescence of the

Synthesis, structural and luminescent aspect of Tb3+ doped Sr2SnO4 phosphor

International Nuclear Information System (INIS)

Taikar, Deepak R.

2016-01-01

A novel green emitting, Tb 3+ doped Sr 2 SnO 4 phosphor was synthesized by the co-precipitation method and its photoluminescence characterization was performed. Sr 2 SnO 4 has an ordered tetragonal K 2 NiF 4 -type structure with space group I4/mmm. The structure of Sr 2 SnO 4 consists of SnO 6 octahedra. From the structure of Sr 2 SnO 4 , it was observed that the sites of Sn 4+ ions have inverse symmetry while the Sr 2+ ions have the low symmetry. X-ray powder diffraction (XRD) analysis confirmed the formation of Sr 2 SnO 4 :Tb 3+ . Photoluminescence measurements showed that the phosphor exhibited bright green emission at about 543 nm attributed to 5 D 4 à 7 F 5 transition of Tb 3+ ion under UV excitation. The emission spectra did not exhibit conventional blue emission peaks of Tb 3+ ions due to 5 D 3 → 7 F J transitions in the spectral region 350-470 nm. The excitation spectra indicate that this compound may be useful as a lamp phosphor. (author)

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

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.)

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.

Photoionization behavior of Eu2+-doped BaMgSiO4 long-persisting phosphor upon UV irradiation

International Nuclear Information System (INIS)

Li, Y.; Wang, Y.; Gong, Y.; Xu, X.; Zhang, F.

2011-01-01

Highlights: → Photoionization behavior of BaMgSiO 4 :Eu 2+ long persistent phosphor upon UV irradiation. → Green phosphorescence was obtained from BaMgSiO 4 :Eu 2+ . → The ionization of Eu 2+ to Eu 3+ was observed in BaMgSiO 4 :Eu 2+ . → The photogenerated Eu 3+ cannot change back to its divalent state at room temperature. → The phosphorescence is associated with the formation forming Eu 3+ -e - pairs. - Abstract: The fluorescence, phosphorescence and thermoluminescence properties of Eu-doped BaMgSiO 4 phosphors sintered in air and in a reducing atmosphere were investigated. Phosphorescence of phosphor sintered in a reducing atmosphere can last for 1.5 h at a recognizable intensity level, whereas phosphorescence of air-sintered phosphor can only persist for 6 min. In addition, a distinction between the shape of the fluorescence spectrum and its corresponding phosphorescence spectrum is observed in the former case. Ionization of Eu 2+ to Eu 3+ upon UV irradiation is observed in the phosphor prepared in a reducing atmosphere, but there is no indication that the photogenerated Eu 3+ cannot change back to its divalent state at room temperature after the excitation source is switched off. In addition, phosphor sintered in a reducing atmosphere shows photochromism upon UV irradiation. No such photoionization and photochromism behavior is observed for the air-sintered phosphor. A possible Eu 2+ photoionization mechanism is constructed on the basis of these experimental observations. The photoionization mechanism presented can also successfully explain the fluorescence and phosphorescence behavior of Eu in BaMgSiO 4 .

Tunable Luminescence of CeAl11O18 Based Phosphors by Replacement of (AlO)+ by (SiN)+ and Co-Doping with Eu

NARCIS (Netherlands)

Yin, L.J.; Chen, G.Z; Wang, C.; Xu, X.; Hao, L.Y.; Hintzen, H.T.J.M.

2014-01-01

A series of Si-N or Eu-Li doped CeAl11O18 and CeAl12O18N phosphors are prepared by solid–state reaction. Their structure and luminescence are researched carefully. Si-N doping with the concentration less than 8% can be successfully dissolved into CeAl11O18 crystal lattice and doesn't change the

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

Tunable emission in Ln3+ (Ce3+/Dy3+, Ce3+/Tb3+) doped KNa3Al4Si4O16 phosphor synthesized by combustion method

Science.gov (United States)

Kolte, M. M.; Pawade, V. B.; Bhattacharya, A. B.; Dhoble, S. J.

2018-05-01

Ln3+ (Ln = Ce3+/Dy3+, Ce3+/Tb3+) doped KNa3Al4Si4O16 phosphor has been synthesized by Combustion method (CS) at 550° C successfully. Ln3+ (Ln = Ce3+, Dy3+, Tb3+) ions when doped in KNa3Al4Si4O16 host lattice, it shows blue and green emission band under the near Ultraviolet (NUV) excitation wavelength. The Photoluminescence excitation (PLE) and emission spectra are observed due to f-f and d-f transition of rare earth ions. Also, an effective energy transfer (ET) study from Ce3+ → Dy3+ and Ce3+ → Tb3+ ions has been studied and confirmed on the basis of Dexter-Foster theory. Further synthesized phosphor is well characterized by XRD, SEM, TEM and decay time measurement. However, the analysis of crystallite size, lattice strain has been studied by using theoretical as well as experimental techniques. Hence, the observed tunable emission in Ln3+ doped KNa3Al4Si4O16 phosphor may be applicable for solid state lighting technology.

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

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).

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.

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.

Phosphorus and Cu2+ removal by periphytic biofilm stimulated by upconversion phosphors doped with Pr3+-Li.

Science.gov (United States)

Zhu, Yan; Zhang, Jianhong; Zhu, Ningyuan; Tang, Jun; Liu, Junzhuo; Sun, Pengfei; Wu, Yonghong; Wong, Po Keung

2018-01-01

Upconversion phosphors (UCPs) can convert visible light into luminescence, such as UV, which can regulate the growth of microbes. Based on these fundamentals, the community composition of periphytic biofilms stimulated by UCPs doped with Pr 3+ -Li + was proposed to augment the removal of phosphorus (P) and copper (Cu). Results showed that the biofilms with community composition optimized by UCPs doped with Pr 3+ -Li + had high P and Cu 2+ removal rates. This was partly due to overall bacterial and algal abundance and biomass increases. The synergistic actions of algal, bacterial biomass and carbon metabolic capacity in the Pr-Li stimulated biofilms facilitated the removal of P and Cu 2+ . The results show that the stimulation of periphytic biofilms by lanthanide-doped UCPs is a promising approach for augmenting P and Cu 2+ removal. Copyright © 2017 Elsevier Ltd. All rights reserved.

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)

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

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

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...

The effect of grain size and phosphorous-doping of polycrystalline 3C–SiC on infrared reflectance spectra

International Nuclear Information System (INIS)

Rooyen, I.J. van; Engelbrecht, J.A.A.; Henry, A.; Janzén, E.; Neethling, J.H.; Rooyen, P.M. van

2012-01-01

Highlights: ► IR is investigated as a technique to measure grain size and P-doping of polycrystalline SiC. ► Infrared plasma minima can be used to determine doping levels in 3C–SiC for doping levels greater than 5 × 10 17 cm −3 . ► A linear relationship is found between FWHM and the inverse of grain size of 3C–SiC irrespective of P-doping level. ► It is further found that ω p is not influenced by the grain size. ► P-doping level has no significant effect on the linear relationship between grain size and surface roughness. - Abstract: The effect of P-doping and grain size of polycrystalline 3C–SiC on the infrared reflectance spectra is reported. The relationship between grain size and full width at half maximum (FWHM) suggest that the behavior of the 3C–SiC with the highest phosphorous doping level (of 1.2 × 10 19 at. cm −3 ) is different from those with lower doping levels ( 18 at. cm −3 ). It is also further demonstrated that the plasma resonance frequency (ω p ) is not influenced by the grain size.

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.

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)

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.

Thermoluminescence kinetic parameters of different amount La-doped ZnB2O4

International Nuclear Information System (INIS)

Kucuk, Nil; Gozel, Aziz Halit; Yüksel, Mehmet; Dogan, Tamer; Topaksu, Mustafa

2015-01-01

The kinetic parameters of 1%, 2%, 3% and 4% La-doped ZnB 2 O 4 phosphors (i.e. ZnB 2 O 4 :0.01La, ZnB 2 O 4 :0.02La, ZnB 2 O 4 :0.03La and ZnB 2 O 4 :0.04La) synthesized by nitric acid method have been calculated. Thermoluminescence (TL) glow curves of ZnB 2 O 4 :La phosphors after beta-irradiation showed a very well defined main peak having the maximum temperature at around 200 °C and a shoulder peak at around 315 °C with a constant heating rate of 5 °C/s. The kinetic parameters of ZnB 2 O 4 :La phosphors TL glow peaks (i.e. order of kinetics (b), activation energies (E a ) and frequency factors (s)) have been determined and evaluated by Computerized Glow Curve Deconvolution (CGCD), and Peak Shape (PS) methods using the glow curve data. From the results, it can conclude that the values of E a obtained with these methods for ZnB 2 O 4 :La phosphors are consistent with each other, but the s values differ considerably. - Highlights: • Calculation of TL kinetic parameters for La-doped ZnB 2 O 4 . • La-doped ZnB 2 O 4 was synthesized by nitric acid method. • Well defined main peak at about 200 °C

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...

UV induced thermoluminescence in rare earth oxide doped phosphors: possible use for UV dosimetry

International Nuclear Information System (INIS)

Yeh, S.-M.; Su, C.-S.

1996-01-01

UV induced thermoluminescent (TL) phenomena in some phosphors doped with rare earth oxides (Gd 2 O 3 :Eu, Gd 2 O 3 :Tb, Gd 2 O 3 :Dy and Y 2 O 3 :EU) have been investigated. Gd 2 O 3 :Eu and Y 2 O 3 :Eu have been found to possess prominent TL phenomena. A stable high temperature glow peak has been found at 345 o C in the cubic (C type) crystalline structure of Gd 2 O 3 :Eu. A more stable high temperature glow peak has also been found at about 380 o C in Y 2 O 3 :Eu. The sensitivity is high enough to be used as UV sensors. TL phenomena in Gd 2 O 3 :Tb and Gd 2 O 3 :Dy have also been investigated, but their TL intensities are much weaker than that of Gd 2 O 3 :Eu or Y 2 O 3 :Eu. On the other hand, all glow peaks of Gd 2 O 3 :Tb and Gd 2 O 3 :Dy are unstable at room temperature, therefore, Gd 2 O 3 :Tb and Gd 2 O 3 :Dy are not suitable for use as UV detectors. According to the above properties, the C type (cubic) crystalline structure of the Gd 2 O 3 :Eu phosphor seems to possess the potential of being the TL material for UV measurement. The position of the high temperature glow peak depends on the total UV exposure. It locates at about 380 o C when this phosphor was irradiated by 302 nm UV at 2.4 mJ.cm -2 exposure, but it shifts to 345 o C at 19.2 mJ.cm -2 or higher exposure. The response curves of this phosphor for various wavelengths, e.g. 253.7 nm, 302 nm, and 365 nm, were also measured. This phosphor is sensitive enough to measure background UV radiations, such as sunlight, bulb light etc. (author)

Cross-linked polybenzimidazole membranes for high temperature proton exchange membrane fuel cells with dichloromethyl phosphinic acid as a cross-linker

DEFF Research Database (Denmark)

Noye, Pernille; Li, Qingfeng; Pan, Chao

2008-01-01

Phosphoric acid doped polybenzimidazole (PBI) membranes have been covalently cross-linked with dichloromethyl phosphinic acid (DCMP). FT-IR measurements showed new bands originating from bonds between the hydrogen bearing nitrogen in the imidazole group of PBI and the CH2 group in DCMP. The produ......Phosphoric acid doped polybenzimidazole (PBI) membranes have been covalently cross-linked with dichloromethyl phosphinic acid (DCMP). FT-IR measurements showed new bands originating from bonds between the hydrogen bearing nitrogen in the imidazole group of PBI and the CH2 group in DCMP.......e. within the temperature range of operation of PBI-based fuel cells....

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)

Long-wave UVA radiation excited warm white-light emitting NaGdTiO{sub 4}: Tm{sup 3+}/Dy{sup 3+}/Eu{sup 3+} ions tri-doped phosphors: Synthesis, energy transfer and color tunable properties

Energy Technology Data Exchange (ETDEWEB)

Bharat, L. Krishna; Du, Peng; Yu, Jae Su, E-mail: jsyu@khu.ac.kr

2016-05-05

NaGdTiO{sub 4} (NGT) phosphors doped with different activator ions (Tm{sup 3+}, Dy{sup 3+}, and Eu{sup 3+}) were synthesized by a conventional solid-state reaction method in an ambient atmosphere. These phosphors were characterized by scanning electron microscope images, transmission electron microscope images, X-ray diffraction patterns, Fourier transform infrared spectra, and photoluminescence spectra. All the samples were crystallized in an orthorhombic phase with a space group of Pbcm (57). In Tm{sup 3+}/Dy{sup 3+} ions co-doped samples, white-light emission was observed under near-ultraviolet (NUV) excitation. In addition, the energy transfer between Tm{sup 3+} and Dy{sup 3+} ions was proved to be a resonant type via an electric dipole–dipole mechanism and the critical distance of energy transfer was calculated to be 19.91 Å. Furthermore, Tm{sup 3+}/Dy{sup 3+}/Eu{sup 3+} ions tri-doped NGT phosphors demonstrated warm white-light emission by appropriately tuning the activator content, based on the principle of energy transfer. These NUV wavelength excitable phosphors exhibit great potential as a single-phase full-color emitting phosphor for white light-emitting diode applications. - Highlights: • The pebble shaped NaGdTiO{sub 4} particles were prepared by solid-state reaction method. • Tm{sup 3+} and Dy{sup 3+} single doping gives respective blue and cool white light emission. • The Tm{sup 3+}/Dy{sup 3+} ions co-doped samples give CIE values near to standard white light. • Addition of Eu{sup 3+} ions shifts the CIE values towards warm white light region. • This single phase white light emitting phosphors have lower CCT values (<5000 K).

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

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

Oxygen- and nitrogen-co-doped activated carbon from waste particleboard for potential application in high-performance capacitance

International Nuclear Information System (INIS)

Shang, Tong-Xin; Ren, Ru-Quan; Zhu, Yue-Mei; Jin, Xiao-Juan

2015-01-01

Graphical abstract: All electrodes showed excellent capacitance and retention versus discharge current density from 0.05 to 5 A/g. - Abstract: Oxygen- and nitrogen-co-doped activated carbons were obtained from phosphoric acid treated nitrogen-doped activated carbons which were prepared from waste particleboard bonded with urea-formaldehyde resin adhesives. The activated carbon samples obtained were tested as supercapacitors in two-electrode cell and extensive wetting 7 M KOH electrolytes. Their structural properties and surface chemistry, before the electrical testing, were investigated using elemental analysis, X-ray photoelectron spectroscopy, scanning electron microscopy, X-ray diffraction, Raman spectra, and adsorption of nitrogen. Activated carbon treated by 4 M phosphoric acid of the highest capacitance (235 F/g) was measured in spite of a relatively lower surface (1360 m 2 /g) than that of the activated carbon treated by 2 M phosphoric acid (1433 m 2 /g). The surface chemistry, and especially oxygen- and nitrogen-containing functional groups, was found of paramount importance for the capacitive behavior and for the effective pore space utilization by the electrolyte ions

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

Preparation and luminescence properties of Eu2+-doped CaSi2O2-dN2+2/3d phosphors

International Nuclear Information System (INIS)

Gu Yunxin; Zhang Qinghong; Wang Hongzhi; Li Yaogang

2009-01-01

Eu 2+ -doped CaSi 2 O 2-d N 2+2/3d phosphors for white LED lamps were prepared by solid-state reaction, and the effects of heat-treatment conditions and the overall composition of host lattice on the optical properties have been discussed. Eu 2+ -doped CaSi 2 O 2-d N 2+2/3d displayed a single broad emission band peak at 540 nm, which could be assigned to the allowed transition of Eu 2+ from the lowest crystal field component of 4f 6 5d to 4f 7 ground-state level. The excitation band of samples, extending from UV to blue, is extremely wide, so the phosphors are suitable for white LED lamps in combination with a UV or blue LED dies. The highest PL intensity is found for the sample sintered at 1400 0 C. Moreover, the emission intensity decreases when N partially replaces O. A red shift of emission wavelength did not occur with increasing of the N content.

Effect of grinding on photostimuable phosphors for x-ray screens

International Nuclear Information System (INIS)

Rao, R.B.

1988-01-01

Luminescence efficiency of a phosphor can be improved by minimizing the energy losses during excitation. The loss of excitation energy in the case of powdered samples is mainly due to scattering of incident radiation by the particles of phosphor. Thus, while considering the industrial applications of polycrystalline phosphors in lamps, screens, paints, etc., the effect of particle size on the light output has to be specially studied. It is very well established that the radiographic imaging with photostimuable (PS) phosphors has many advantages over conventional photographic film screens. In the new type of computer radiography, PS phosphors are to be used as memory materials for temporary storage of the x-ray image. Eu(2+) doped barium fluorohalide phosphors are most suitable for this purpose. The spatial resolution from the image plate can be improved to a certain extent with phosphors comprising fine particles. The fineness of the particles can be achieved by various means such as grinding, fast cooling after firing or incorporation of some flux materials during the firing processes. But the efficiency of the phosphor deteriorates with grinding. Fast cooling is a complicated process in the case of Eu(2+) doped phosphors. Incorporation of flux materials may change the characteristics of phosphor materials. In the present investigation, effect of grinding (ball milling) on particle size distribution, shape of the particles and luminescent properties of BaFCl phosphors have been studied

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.

Energy transfer and color tunable emission in Tb3+,Eu3+ co-doped Sr3LaNa(PO4)3F phosphors.

Science.gov (United States)

Li, Shuo; Guo, Ning; Liang, Qimeng; Ding, Yu; Zhou, Huitao; Ouyang, Ruizhuo; Lü, Wei

2018-02-05

A group of color tunable Sr 3 LaNa(PO 4 ) 3 F:Tb 3+ ,Eu 3+ phosphors were prepared by conventional high temperature solid state method. The phase structures, luminescence properties, fluorescence lifetimes and energy transfer were investigated in detail. Under 369nm excitation, owing to efficient energy transfer of Tb 3+ →Eu 3+ , the emission spectra both have green emission of Tb 3+ and red emission of Eu 3+ . An efficient energy transfer occur in Tb 3+ , Eu 3+ co-doped Sr 3 LaNa(PO 4 ) 3 F phosphors. The most possible mechanism of energy transfer is dipole-dipole interaction by Dexter's theoretical model. The energy transfer of Tb 3+ and Eu 3+ was confirmed by the variations of emission and excitation spectra and Tb 3+ /Eu 3+ decay lifetimes in Sr 3 LaNa(PO 4 ) 3 F:Tb 3+ ,Eu 3+ . The color tone can tuned from yellowish-green through yellow and eventually to reddish-orange with fixed Tb 3+ content by changing Eu 3+ concentrations. The results show that the prepared Tb 3+ , Eu 3+ co-doped color tunable Sr 3 LaNa(PO 4 ) 3 F phosphor can be used for white LED. Copyright © 2017 Elsevier B.V. All rights reserved.

Energy transfer and color tunable emission in Tb3 +,Eu3 + co-doped Sr3LaNa(PO4)3F phosphors

Science.gov (United States)

Li, Shuo; Guo, Ning; Liang, Qimeng; Ding, Yu; Zhou, Huitao; Ouyang, Ruizhuo; Lü, Wei

2018-02-01

A group of color tunable Sr3LaNa(PO4)3F:Tb3 +,Eu3 + phosphors were prepared by conventional high temperature solid state method. The phase structures, luminescence properties, fluorescence lifetimes and energy transfer were investigated in detail. Under 369 nm excitation, owing to efficient energy transfer of Tb3 + → Eu3 +, the emission spectra both have green emission of Tb3 + and red emission of Eu3 +. An efficient energy transfer occur in Tb3 +, Eu3 + co-doped Sr3LaNa(PO4)3F phosphors. The most possible mechanism of energy transfer is dipole-dipole interaction by Dexter's theoretical model. The energy transfer of Tb3 + and Eu3 + was confirmed by the variations of emission and excitation spectra and Tb3 +/Eu3 + decay lifetimes in Sr3LaNa(PO4)3F:Tb3 +,Eu3 +. The color tone can tuned from yellowish-green through yellow and eventually to reddish-orange with fixed Tb3 + content by changing Eu3 + concentrations. The results show that the prepared Tb3 +, Eu3 + co-doped color tunable Sr3LaNa(PO4)3F phosphor can be used for white LED.

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)

The effect of grain size and phosphorous-doping of polycrystalline 3C-SiC on infrared reflectance spectra

Energy Technology Data Exchange (ETDEWEB)

Rooyen, I.J. van, E-mail: Isabella.vanRooyen@inl.gov [Fuel Performance and Design Department, Idaho National Laboratory, Idaho Falls, ID 83415-6188 (United States); Department of Physics, Nelson Mandela Metropolitan University, Port Elizabeth (South Africa); Engelbrecht, J.A.A. [Department of Physics, Nelson Mandela Metropolitan University, Port Elizabeth (South Africa); Henry, A.; Janzen, E. [Department of Physics, Chemistry and Biology, Semiconductor Materials, Linkoeping University, Linkoeping 58183 (Sweden); Neethling, J.H. [Department of Physics, Nelson Mandela Metropolitan University, Port Elizabeth (South Africa); Rooyen, P.M. van [Philip M van Rooyen Network Consultants, Midlands Estates (South Africa)

2012-03-15

Highlights: Black-Right-Pointing-Pointer IR is investigated as a technique to measure grain size and P-doping of polycrystalline SiC. Black-Right-Pointing-Pointer Infrared plasma minima can be used to determine doping levels in 3C-SiC for doping levels greater than 5 Multiplication-Sign 10{sup 17} cm{sup -3}. Black-Right-Pointing-Pointer A linear relationship is found between FWHM and the inverse of grain size of 3C-SiC irrespective of P-doping level. Black-Right-Pointing-Pointer It is further found that {omega}{sub p} is not influenced by the grain size. Black-Right-Pointing-Pointer P-doping level has no significant effect on the linear relationship between grain size and surface roughness. - Abstract: The effect of P-doping and grain size of polycrystalline 3C-SiC on the infrared reflectance spectra is reported. The relationship between grain size and full width at half maximum (FWHM) suggest that the behavior of the 3C-SiC with the highest phosphorous doping level (of 1.2 Multiplication-Sign 10{sup 19} at. cm{sup -3}) is different from those with lower doping levels (<6.6 Multiplication-Sign 10{sup 18} at. cm{sup -3}). It is also further demonstrated that the plasma resonance frequency ({omega}{sub p}) is not influenced by the grain size.

Structural and optical investigation in Er3+ doped Y2MoO6 phosphors

Science.gov (United States)

Mondal, Manisha; Rai, Vineet Kumar

2018-05-01

The Er3+ doped Y2MoO6 phosphors have been structurally and optically characterized by X-ray Diffraction (XRD), Field emission scanning electron microscopy (FESEM), UV-Vis absorption spectroscopy and frequency upconversion (UC) emission studies. The crystal and the particles size are found to be ˜ 85 nm and ˜ 200 nm from XRD and FESEM analysis. The intense peak at ˜ 206 nm in the UV-Vis absorption spectroscopy is attributed due to the charge transfer transition between the Mo6+ and the O2- ions in the MoO4 group in the host molybdate. The frequency UC emission studies of the prepared phosphors under 980 nm diode laser excitation shows the intense UC emission in the 0.3 mol% concentrations for the Er3+ ions. In the UC emission spectra, the emission peaks at green (˜ 525 nm and ˜ 546 nm) and red (˜ 656 nm) bands are corresponding to the 2H11/2, 4S3/2 → 4I15/2 and 4F9/2 → 4I15/2 transitions of Er3+ ions. The mechanisms involved in the UC process have been explored with the help of energy level diagram. Moreover, the CIE point (0.31, 0.60) lie in the green colour region which indicates that the developed phosphor have suitable applications in NIR to visible upconverter and in making green light display devices.

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)

Phase transition and multicolor luminescence of Eu2+/Mn2+-activated Ca3(PO4)2 phosphors

International Nuclear Information System (INIS)

Li, Kai; Chen, Daqin; Xu, Ju; Zhang, Rui; Yu, Yunlong; Wang, Yuansheng

2014-01-01

Graphical abstract: We have synthesized Eu 2+ doped and Eu 2+ /Mn 2+ co-doped Ca 3 (PO 4 ) 2 phosphors. The emitting color varies from blue to green with increasing of Eu 2+ content for the Eu 2+ -doped phosphor, and the quantum yield of the 0.05Eu 2+ : Ca 2.95 (PO 4 ) 2 sample reaches 56.7%. Interestingly, Mn 2+ co-doping into Eu 2+ : Ca 3 (PO 4 ) 2 leads to its phase transition from orthorhombic to rhombohedral, and subsequently generates tunable multi-color luminescence from green to red via Eu 2+ → Mn 2+ energy transfer. - Highlights: • A series of novel Eu 2+ : Ca 3 (PO 4 ) 2 phosphors were successfully synthesized. • Phase transition of Ca 3 (PO 4 ) 2 from orthorhombic to rhombohedral occurred when Mn 2+ ions were doped. • The phosphors exhibited tunable multi-color luminescence. • The quantum yield of 0.05Eu 2+ : Ca 2.95 (PO 4 ) 2 phosphor can reach 56.7%. • The analyses of phosphors were carried out by many measurements. - Abstract: Intense blue-green-emitting Eu 2+ : Ca 3 (PO 4 ) 2 and tunable multicolor-emitting Eu 2+ /Mn 2+ : Ca 3 (PO 4 ) 2 phosphors are prepared via a solid-state reaction route. Eu 2+ -doped orthorhombic Ca 3 (PO 4 ) 2 phosphor exhibits a broad emission band in the wavelength range of 400–700 nm with a maximum quantum yield of 56.7%, and the emission peak red-shifts gradually from 479 to 520 nm with increase of Eu 2+ doping content. Broad excitation spectrum (250–420 nm) of Eu 2+ : Ca 3 (PO 4 ) 2 matches well with the near-ultraviolet LED chip, indicating its potential applications as tri-color phosphors in white LEDs. Interestingly, Mn 2+ co-doping into Eu 2+ : Ca 3 (PO 4 ) 2 leads to its phase transition from orthorhombic to rhombohedral, and subsequently generates tunable multi-color luminescence from green to red via Eu 2+ → Mn 2+ energy transfer, under 365 nm UV lamp excitation

Rare-earth doped gadolinia based phosphors for potential multicolor and white light emitting deep UV LEDs.

Science.gov (United States)

Bedekar, Vinila; Dutta, Dimple P; Mohapatra, M; Godbole, S V; Ghildiyal, R; Tyagi, A K

2009-03-25

Gadolinium oxide host and europium/dysprosium/terbium doped gadolinium oxide nanoparticles were synthesized using the sonochemical technique. Gadolinium oxide nanocrystals were also co-doped with total 2 mol% of Eu(3+)/Dy(3+),Eu(3+)/Tb(3+),Dy(3+)/Tb(3+), and also Eu(3+)/Dy(3+)/Tb(3+) ions, by the same method. The nanoparticles obtained were characterized using powder x-ray diffraction (XRD), transmission electron microscopy (TEM), and selected area electron diffraction (SAED) techniques. The size of the particles ranged from 15 to 30 nm. The triple doped samples showed multicolor emission on single wavelength excitation. The photoluminescence results were correlated with the lifetime data to get an insight into the luminescence and energy transfer processes taking place in the system. On excitation at 247 nm, the novel nanocrystalline Gd(2)O(3):RE (RE = Dy, Tb) phosphor resulted in having very impressive CIE chromaticity coordinates of x = 0.315 and y = 0.316, and a correlated color temperature of 6508 K, which is very close to standard daylight.

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

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

Temperature Mapping of Air Film-Cooled Thermal Barrier Coated Surfaces Using Cr-Doped GdAlO3 Phosphor Thermography

Science.gov (United States)

Eldridge, Jeffrey I.; Shyam, Vikram; Wroblewski, Adam C.; Zhu, Dongming; Cuy, Michael D.; Wolfe, Douglas E.

2016-01-01

It has been recently shown that the high luminescence intensity from a Cr-doped GdAlO3 (Cr:GdAlO3) thermographic phosphor enables non-rastered full-field temperature mapping of thermal barrier coating (TBC) surfaces to temperatures above 1000C. In this presentation, temperature mapping by Cr:GdAlO3 based phosphor thermometry of air film-cooled TBC-coated surfaces is demonstrated for both scaled-up cooling hole geometries as well as for actual components in a burner rig test environment. The effects of thermal background radiation and flame chemiluminescence on the measurements are investigated, and advantages of this method over infrared thermography as well as the limitations of this method for studying air film cooling are discussed.

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)

Eu{sup 2+}-doped OH{sup −} free calcium aluminosilicate glass: A phosphor for smart lighting

Energy Technology Data Exchange (ETDEWEB)

Lima, S.M., E-mail: smlima@uems.br [Grupo de Espectroscopia Óptica e Fototérmica, Universidade Estadual de Mato Grosso do Sul, C. P. 351, CEP 79804-970 Dourados, MS (Brazil); Andrade, L.H.C.; Rocha, A.C.P. [Grupo de Espectroscopia Óptica e Fototérmica, Universidade Estadual de Mato Grosso do Sul, C. P. 351, CEP 79804-970 Dourados, MS (Brazil); Silva, J.R.; Farias, A.M.; Medina, A.N.; Baesso, M.L. [Departamento de Física, Universidade Estadual de Maringá, Av. Colombo 5790, 87020-900 Maringá, PR (Brazil); Nunes, L.A.O. [Instituto de Física de São Carlos, Universidade de São Paulo, 13560-970 São Carlos, SP (Brazil); Guyot, Y.; Boulon, G. [Laboratoire de Physico-Chimie des Matériaux Luminescents, Université de Lyon 1, UMR 5620 CNRS, 69622 Villeurbanne (France)

2013-11-15

In this paper, a broad emission band from Eu{sup 2+}-doped OH{sup −} free calcium aluminosilicate glass is reported. By changing the excitation wavelengths, the results showed it is possible to tune the emission from green to orange, what combined with the scattered light from the same blue LED used for excitation, provided a color rendering index of 71 and a correlated color temperature of 6550 K. Our preliminary tests indicate this material as a promising phosphor towards the development of smart lighting devices. -- Highlights: • We report a broad emission band from Eu{sup 2+}-doped OH{sup −} free calcium aluminosilicate glass. • The maximum emission peak can be tune from green to orange region. • The test with a LED provided a color rendering index of 71 and a correlated color temperature of 6550 K.

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.

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

Electrocatalytic and supercapacitor performance of Phosphorous and Nitrogen co-doped Porous Carbons synthesized from Aminated Tannins

International Nuclear Information System (INIS)

Bairi, Venu Gopal; Nasini, Udaya B.; Kumar Ramasahayam, Sunil; Bourdo, Shawn E.; Viswanathan, Tito

2015-01-01

Highlights: • Microwave Synthetic technique using aminated tannins is reported for the first time. • P,N doped carbon was characterized extensively for physico-chemical properties. • Cyclic Voltammetry, RDE and RRDE studies were investigated for O 2 reduction capability. • O 2 reduction occurred by a kinetically favored one step four electron reduction pathway. • The charge storage capacity was found to be 161 F/g at 5 mV/S in alkaline conditions. - Abstract: A phosphorus and nitrogen co-doped carbon material (PNDC) was synthesized from aminated tannin and polyphosphoric acid by a rapid and highly efficient microwave synthetic technique. X-ray photoelectron spectroscopy study was useful in the identification of nitrogen and phosphorous environments in a sp 2 hybridized carbon lattice. The PNDC was found to be a porous material with a surface area of 433 m 2 g −1 . PNDC sample exhibited excellent thermal stability and the Raman spectroscopic studies were used for analyzing defects in the sp 2 hybridized carbon lattice. This material has promising electrochemical applications, especially for catalyzing oxygen reduction reaction in fuel cells and for charge storage in supercapacitors. The oxygen reduction capability of PNDC was investigated in 0.1 M KOH solution, and rotating disk and ring disk electrode studies were performed to identify the mechanism of oxygen reduction. The capacitative behavior of the PNDC was investigated in 6 M KOH and specific capacitance was determined to be 161 F g −1 due to the electric double layer charge storage phenomenon.

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

Fracto- mechanoluminescence and thermoluminescence properties of orange-red emitting Eu3+ doped Ca2Al2SiO7 phosphors

International Nuclear Information System (INIS)

Tiwari, Geetanjali; Brahme, Nameeta; Sharma, Ravi; Bisen, D.P.; Sao, Sanjay K.; Khare, Ayush

2017-01-01

The suitability of nano-structured Ca 2 Al 2 SiO 7 :Eu 3+ phosphors for thermoluminescence and mechanoluminescence dosimeter were investigated. Europium doped di-calcium di-aluminum silicate phosphor was synthesised by the combustion assisted method and annealed at 1100 °C for 4 h in reducing and oxidizing environments. The prepared Ca 2 Al 2 SiO 7 :Eu 3+ phosphor was characterized by X-ray diffractometer (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) with energy dispersive x-ray spectroscopy (EDX), photoluminescence (PL) and decay characteristics. The phase structure of sintered phosphor has akermanite type which belongs to the tetragonal crystallography; this structure is a member of the melilite group and forms a layered compound. The chemical composition of the sintered Ca 2 Al 2 SiO 7 :Eu 3+ phosphor was confirmed by EDX spectra. Mechanoluminescence (ML) and thermoluminescence (TL) studies revealed that the ML and TL intensity increases with activator concentration. Optimum ML was observed for the sample having 2 mol% of Eu ions. The TL intensity of Ca 2 Al 2 SiO 7 :Eu 3+ was recorded for different exposure times of γ -irradiation and it was observed that TL intensity is maximum for γ dose of 1770 Gy. The PL spectra indicated that Ca 2 Al 2 SiO 7 :Eu 3+ could be excited effectively by near ultraviolet (NUV) light and exhibited bright orange-red emission with excellent colour stability. CIE colour coordinates of the prepared Ca 2 Al 2 SiO 7 :Eu 3+ phosphor was found suitable as orange-red light emitting phosphor with a CIE value of (x=0.6142, y=0.3849) and correlated colour temperature (CCT) is 1250 K. Therefore, it is considered to be a new promising orange-red emitting phosphor for white light emitting diode (LED) application.

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

Micro/nano phosphors for gamma, electron, fast and thermal neutron dosimetry: an overview

International Nuclear Information System (INIS)

Dhole, Sanjay D.

2016-01-01

In this talk an overview of the micro/nano phosphors, nuclear track in glass and Fricke dosimeter will be covered. Eu and Cu doped K_2Ca_2(SO_4)_3 by chemical co-precipitation, CaSO_4:Dy (micro by acid re-crystallization method and Al_2O_3:C by Thermal Plasma reactor method were synthesized and their photoluminescence (PL), Thermoluminescence (TL) and Optically Stimulated Luminescence (OSL) properties were characterized

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

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...

Luminescence properties of Nd{sup 3+}-doped (Y,Gd)BO{sub 3} phosphors

Energy Technology Data Exchange (ETDEWEB)

Yi, Soung Soo; Kim, Ji-Chul; Kim, Dong Woo [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Balakrishnaiah, R. [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Kim, Sung Hoon [Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of); Jang, Kiwan, E-mail: kwjang@changwon.ac.k [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Lee, Ho Sueb [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Moon, Byung Kee; Jeong, Jung Hyun [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of)

2010-09-01

A system of 0.03 mol Nd{sup 3+}-doped (Y,Gd)BO{sub 3} phosphors were prepared by the conventional solid state reaction method for different concentrations of Gd{sup 3+} ions and were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and NIR emission measurements. The emitted radiation was dominated by 1057 nm peak in the NIR region as a result of {sup 4}F{sub 3/2} {yields} {sup 4}I{sub 11/2} transitions of Nd{sup 3+} ions. As the concentration of Gd{sup 3+} ions increases from 0.00 to 0.57 mol, the grain sizes and the intensity of NIR emission peaks were improved. The results are discussed in comparison with similar reported works.

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

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.

Structural characterization and optical properties of Eu"2"+ and Dy"2"+ doped Sr_2SiO_4 phosphor by solid state reaction method

International Nuclear Information System (INIS)

Verma, Durga; Verma, Mohan L.; Upma; Patel, R.P.

2016-01-01

Thermoluminescence, SEM, FTIR Divalent dysprosium and europium doped strontium silicate (Sr_2SiO_4) phosphors were synthesized with the high-temperature solid-state reaction technique. The obtained phosphor was well characterized by powder X-ray diffraction, scanning electron microscopy, FTIR, UV-visible spectroscopy and thermoluminescence. The crystal structure of the prepared phosphor has an orthorhombic structure with space group Pnma. From scanning electron microscopy (SEM), agglomerations of particles were observed due to the high temperature synthesis process. The chemical composition of the sintered Sr_2SiO_4:Dy"2"+ and Sr_2SiO_4: Eu"2"+ phosphor was confirmed by energy dispersive X-ray spectroscopy (EDX). The UV-VIS analysis can be thought as a good quality check for the optical behavior of materials. The Fourier transmission infrared spectroscopy (FTIR) confirms the present elements in phosphor. Thermoluminescence study was carried out for the phosphor with UV irradiation show one glow peak. The trapping parameters associated with the prominent glow peak of Sr_2SiO_4:Dy"2"+ and Sr_2SiO_4:Eu"2"+ are calculated using Chen's glow curve method. The release of holes/electrons from defect centers at the characteristic trap site initiates the luminescence process in this material. (author)

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

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.

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]).

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.

Luminescence properties of Eu{sup 2+} doped SrB{sub 4}O{sub 7} phosphor for radiation dosimetry

Energy Technology Data Exchange (ETDEWEB)

Palan, C.B., E-mail: chetanpalan27@yahoo.in; Bajaj, N.S.; Omanwar, S.K.

2016-04-15

Highlights: • Report TL/OSL properties of SrB{sub 4}O{sub 7}:Eu{sup 2+} under beta irradiations. • OSL Sensitivity was about 33% than that of commercially available α-Al{sub 2}O{sub 3.} • TL glow peaks was appear at 305° C and TL sensitivity about 200 times higher than TLD-500. • OSL decay pattern was faster than α- Al{sub 2}O{sub 3}:C and dose response was linear nature. - Abstract: In this report, we presented the TL/OSL properties of Eu doped SrB{sub 4}O{sub 7} phosphor under β-irradiation. This phosphor was synthesized by using solid state method. The phosphor shows OSL sensitivity about 33% than that of commercially available α-Al{sub 2}O{sub 3}: C phosphor. CW-OSL curve possess two components having photoionization cross-sections 0.707 × 10{sup −17} and 18.58 × 10{sup −17} cm{sup 2} respectively and TL sensitivity about 200 times higher than TLD-500. The kinetic parameters such as activation energy, frequency factor and order of kinetics of TL curve were calculated by using peak shape method. In TL/OSL mode dose-response was almost linear in the range of measurements. The MDD was found to be 1.26 mGy with 3σ of background. Also reusability studies showed the phosphor can be reused for 10 cycles with 1% change in the OSL output. The PL spectra of SrB{sub 4}O{sub 7} showed emission in NUV region when excited with 318 nm under UV source.

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 ...

The synthesis and luminescence properties of a novel red-emitting phosphor. Eu{sup 3+}-doped Ca{sub 9}La(PO{sub 4}){sub 7}

Energy Technology Data Exchange (ETDEWEB)

Liang, Zehui [Guangdong University of Technology, Experimental Teaching Department, Guangzhou (China); Guangdong University of Technology, School of Chemical Engineering and Light Industry, Guangzhou (China); Mu, Zhongfei; Zhu, Daoyun [Guangdong University of Technology, Experimental Teaching Department, Guangzhou (China); Wang, Qiang; Wu, Fugen [Guangdong University of Technology, School of Materials and Energy, Guangzhou (China)

2017-10-15

A series of novel red-emitting phosphors Ca{sub 9}La{sub 1-x}(PO{sub 4}){sub 7}: xEu{sup 3+} were synthesized by high-temperature solid state reactions. The photoluminescence excitation and photoluminescence spectra of these phosphors were investigated in detail. O{sup 2-}-Eu{sup 3+} charge transfer band peaking at about 261 nm is dominant in the PLE spectra of Eu{sup 3+}-doped Ca{sub 9}La(PO{sub 4}){sub 7}, indicating that the phosphors are suitable for tricolor fluorescent lamps. The phosphors also show a good absorption in near ultraviolet (around 395 nm) and blue (around 465 nm) spectral region, which indicates that it can be pumped with NUV and blue chips for white light-emitting diodes. The transition of {sup 5}D{sub 0} → {sup 7}F{sub 2} of Eu{sup 3+} in this lattice can emit bright red light. Ca{sub 9}La(PO{sub 4}){sub 7} could accommodate a large amount of Eu{sup 3+} with an optimal concentration of 60 mol%. The dipole-dipole interaction between Eu{sup 3+} is the dominant mechanism for concentration quenching of Eu{sup 3+}. The calculated color coordinates lie in red region (x = 0.64, y = 0.36), which is close to Y{sub 2}O{sub 3}: 0.05Eu{sup 3+} (x = 0.65, y = 0.34). The integral emission intensity of Ca{sub 9}La{sub 0.4}(PO{sub 4}){sub 7}: 0.6Eu{sup 3+} is 1.9 times stronger than that of widely used commercial red phosphor Y{sub 2}O{sub 3}: 0.05Eu{sup 3+}. All these results indicate that Eu{sup 3+}-doped Ca{sub 9}La(PO{sub 4}){sub 7} is a promising red-emitting phosphor which can be used in tricolor fluorescent lamps and white light-emitting diodes. (orig.)

Luminescence properties of CdSiO3:Mn2+ phosphor

International Nuclear Information System (INIS)

Lei Bingfu; Liu Yingliang; Ye Zeren; Shi Chunshan

2004-01-01

A novel long-lasting phosphor CdSiO 3 :Mn 2+ is reported in this paper. The Mn 2+ -doped CdSiO 3 phosphor emits orange light with CIE chromaticity coordinates x=0.5814 and y=0.4139 under 254 nm UV light excitation. In the emission spectrum of 1% Mn 2+ -doped CdSiO 3 phosphor, there is a broad emission band centered at 575 nm which can be attributed to the spin-forbidden transition of the d-orbital electron associated with the Mn 2+ ion. The phosphorescence can be seen by the naked eyes in the dark clearly even after the 254 nm UV irradiation have been removed for about 1 h. The mechanism of the origin of the long-lasting phosphorescence was discussed using the thermoluminescence curves

Synthesis and Luminescence Properties of Novel Ce(3+)- and Eu(2+)-Doped Lanthanum Bromothiosilicate La3Br(SiS4)2 Phosphors for White LEDs.

Science.gov (United States)

Lee, Szu-Ping; Liu, Shuang-De; Chan, Ting-Shan; Chen, Teng-Ming

2016-04-13

Novel Ce(3+)- and Eu(2+)-doped lanthanum bromothiosilicate La3Br(SiS4)2:Ce(3+)and La3Br(SiS4)2:Eu(2+) phosphors were prepared by solid-state reaction in an evacuated and sealed quartz glass ampule. The La3Br(SiS4)2:Ce(3+) phosphor generates a cyan emission upon excitation at 375 nm, whereas the La3Br(SiS4)2:Eu(2+) phosphor could be excited with extremely broad range from UV to blue region (300 to 600 nm) and generates a reddish-orange broadband emission centered at 640 nm. In addition, thermal luminescence properties of La3Br(SiS4)2:Ce(3+)and La3Br(SiS4)2:Eu(2+) phosphors from 20 to 200 °C were investigated. The combination of a 450 nm blue InGaN-based LED chip with the red-emitting La3Br(SiS4)2:Eu(2+) phosphor, and green-emitting BOSE:Eu(2+) commercial phosphor produced a warm-white light with the CRI value of ∼95 and the CCT of 5,120 K. Overall, these results show that the prepared phosphors may have potential applications in pc-WLED.

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.

Spectral-converting behaviors of Er{sup 3+} and Er{sup 3+}–Yb{sup 3+} doped YOCl phosphors

Energy Technology Data Exchange (ETDEWEB)

Park, Sangmoon, E-mail: spark@silla.ac.kr [Center for Green Fusion Technology and Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of); Cho, So-Hye [Center for Materials Architecturing, Institute of Multidisciplinary Convergence of Materials, Korea Institute of Science and Technology, Seoul 130-650 (Korea, Republic of)

2014-01-25

Highlights: • Luminescent materials of YOCl:Er,Yb were prepared using NH{sub 4}Cl flux. • Interesting spectral-converting behaviors were observed in the phosphors. • 980 or 1550 nm diode laser was irradiated for up-converting study. • A multi-photon process in the phosphors was calculated. -- Abstract: Luminescent materials composed of Y{sub 1−m−n}Er{sub m}Yb{sub n}OCl (m = 0.001–0.1, n = 0.005–0.1) were prepared via a solid-state reaction using NH{sub 4}Cl flux. Photoluminescence spectra, the dependence of the luminescent intensity as a function of Er{sup 3+} content, and their CIE coordinates of the Er{sup 3+}-doped layered YOCl compounds were also investigated under near-ultraviolet (NUV) and visible lights. The spectral up-converting properties of Er{sup 3+} and Er{sup 3+}–Yb{sup 3+} in YOCl phosphors were elucidated under 980 and 1550 nm diode laser irradiations. This up-conversion emission spectra and the pump power dependence versus emission intensity observed in the Y{sub 0.9}Er{sub 0.1}OCl up-conversion phosphors gave rise to one- and two-photon processes. The up-conversion mechanism of Er{sup 3+} and Yb{sup 3+} ions in YOCl was described by a schematic energy-level diagram. Through the use of these up-conversion luminescent materials, the desired emitting lights throughout the orange and red regions of the spectra were achieved.

NIR to VIS frequency upconversion luminescence properties of Er{sup 3+}-doped YPO{sub 4} phosphors

Energy Technology Data Exchange (ETDEWEB)

Balakrishnaiah, R. [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Kim, Dong Woo [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Yi, Soung Soo, E-mail: ssyi@silla.ac.k [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Kim, Sung Hoon [Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of); Jang, Kiwan; Lee, Ho Sueb [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Moon, Byung Kee; Jeong, Jung Hyun [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of)

2010-09-01

Different concentrations of Er{sup 3+}-doped YPO{sub 4}:Er powder phosphors have been synthesized by the conventional solid state reaction method and are characterized by X-ray diffraction (XRD), field emission scanning electronic microscopy (FESEM), and upconversion emission measurements. An intense red emission band and a weak green emission band are observed under NIR excitation at 975 nm in case of samples with high dopant concentration while no upconversion emission was observed at lower Er{sup 3+} ion concentrations. The possible mechanisms involved in the upconversion process have been discussed in comparison to results with similar reported works.

Luminescent properties and energy transfer in the green phosphors LaBSiO5:Tb3+, Ce3+.

Science.gov (United States)

Wang, Zhengliang; Cheng, Ping; He, Pei; Liu, Yong; Zhou, Yayun; Zhou, Qiang

2015-09-01

LaBSiO5 phosphors doped with Ce(3+) and Tb(3+) were synthesized using the conventional solid-state method at 1100 °C. The phase purity and luminescent properties of these phosphors are investigated. LaBSiO5:Tb(3+) phosphors show intense green emission, and LaBSiO5 phosphors doped with Ce(3+) show blue-violet emission under UV light excitation. LaBSiO5 phosphors co-doped with Ce(3+) and Tb(3+) exhibit blue-violet and green emission under excitation by UV light. The blue-violet emission is due to the 5d-4f transition of Ce(3+) and the green emission is ascribed to the (5) D4 → (7) F5 transition of Tb(3+). The spectral overlap between the excitation band of Tb(3+) and the emission band of Ce(3+) supports the occurrence of energy transfer from Ce(3+) to Tb(3+), and the energy transfer process was investigated. Copyright © 2014 John Wiley & Sons, Ltd.

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

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...

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)

Luminescence characterization of sol-gel derived Pr"3"+ doped NaGd(WO_4)_2 phosphors for solid state lighting applications

International Nuclear Information System (INIS)

Durairajan, A.; Thangaraju, D.; Moorthy Babu, S.; Valente, M.A.

2016-01-01

In the present work, xPr"3"+:NaGd(WO_4)_2 (0.5 ≤ x ≤ 5.0 mol%) sub-micron phosphors were synthesised by sol-gel method. Low cost precursors of metal nitrates and low temperature thermal treatment was used compared to conventional solid state reaction. The formation of highly crystalline phosphors with tetragonal structure was confirmed by XRD and increase of Pr"3"+ ions content in host matrix leads to expansion of the unit cell volume. The surface morphology, size and particle distribution of the phosphors were observed by field emission scanning electron microscopy (FE-SEM). A rectangular shape particle with a size distribution ranging from 400 to 600 nm and tightly packed surface was seen in FE-SEM micrographs. The various internal and external phonon modes vibration corresponding to double tungstate structure was observed in Raman spectra. The optical properties of the synthesised phosphors were explored by ultraviolet visible (UV–Vis) absorption in diffuse reflectance and photoluminescence (PL) measurements. UV–Vis measurements distinguished the host and Pr"3"+ absorption and also reveal an increase in optical band gap values with an increase of Pr"3"+. The PL measurements show various emissions from green and red regions under 450 nm. The maximum intensity emission at 489 nm is due to "3P_0 → "3H_4 transition of Pr"3"+. From the maximum emission the critical doping concentration was calculated to be at 3.5 mol% and critical distance between two adjacent Pr"3"+ ions as 20.43 Å. - Highlights: • A sol-gel method was used to prepare Pr"3"+ doped NaGd(WO_4)_2 at low temperature. • Structural, spectroscopic, morphological, and optical and luminescence properties were studied. • The praseodymium ions are in trivalent state, the site symmetry is distorted and S_4 local symmetry with Na"+ ions. • Strong green emission was observed under UV and visible excitation.

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.

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.

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)

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.

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.

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.

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.

A novel orange emissive phosphor SrWO4:Sm3+ for white light-emitting diodes

International Nuclear Information System (INIS)

Ju Zhenghua; Wei Ruiping; Ma Jingxin; Pang Chaoran; Liu Weisheng

2010-01-01

Research highlights: → A novel orange emissive phosphor SrWO 4 :Sm 3+ was firstly reported. → The optics properties of Sm 3+ -doped SrWO 4 phosphor were successfully discussed. → The temperature-dependent luminescence indicates the phosphor exhibits a small thermal-quenching property. → The phosphor is a potential candidate as orange-emitting component for white LED. - Abstract: A novel orange emissive phosphor, Sm 3+ -doped SrWO 4 , was synthesized by high temperature solid-state reaction in air atmosphere. The excitation spectra show that the phosphors can be efficiently excited by ultraviolet and near-ultraviolet light, the optimized concentration is 4 mol%. Three emission peaks locate at 562, 596 and 642 nm, corresponding to CIE chromaticity coordinates of (x = 0.54, y = 0.46), which indicates the orange light emitting. The decay curves are well fitted with triple-exponential decay models. The quantum yield of the Sr 0.96 Sm 0.04 WO 4 phosphor is about 70.65% under excitation of 377 nm. Furthermore, the temperature-dependent luminescence indicates the phosphor exhibits a small thermal-quenching property. So the phosphor is able to be applied to UV-LED chip-based white light-emitting diodes.

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

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'.

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.

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

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.

Effect of synthesis methods on luminescence properties of LiCaPO{sub 4}:Ce phosphor for radiation dosimetry

Energy Technology Data Exchange (ETDEWEB)

Palan, C.B., E-mail: chetupalan@rediffmail.com; Omanwar, S.K.

2016-10-15

The polycrystalline doped and un-doped LiCaPO{sub 4} phosphors were successfully prepared via solid state diffusion [SSD] and sol–gel [SG] methods. The sol–gel method was implied to decrease the processing time and heating temperature. The prepared un-doped and doped LiCaPO{sub 4} phosphors were characterized through X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. Additionally photoluminescence (PL), thermoluminescence (TL) and optically stimulated luminescence (OSL) properties were studied. The XRD patterns of prepared LiCaPO{sub 4} and LiCaPO{sub 4}:Ce phosphors were well matched with the ICDD file. The average particles size of LiCaPO{sub 4} and LiCaPO{sub 4}:Ce phosphors were found to be in the range 2–10 μm by SSD method and 2-5 μm by SG method. The excitation spectra of LiCaPO{sub 4} and LiCaPO{sub 4}:Ce phosphors consist of broad band in the range 200–330 nm and maximum intensity was observed at 314 nm. Also emission spectra consist of broad band in range from 330–500 nm and maximum intensity was observed at 369 nm. With the increase of Ce{sup 3+} ions concentration, the emission spectra of LiCaPO{sub 4}:Ce{sup 3+} phosphors shifted to a longer wavelength. The prepared phosphors were showed excellent TL properties under β irradiation. The OSL sensitivity of the LiCaPO{sub 4}:Ce phosphor synthesized by the SSD method was the nearly same as compared with the OSL sensitivity of LiCaPO{sub 4}:Ce phosphor synthesized by the SG method.

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.

Spectral downshifting in MBO{sub 3}:Nd{sup 3+} (M=Y, La) phosphor

Energy Technology Data Exchange (ETDEWEB)

Omanwar, S.K.; Sawala, N.S. [Sant Gadge Baba Amravati University, Department of Physics, Amravati, MH (India)

2017-11-15

The spectral downshifting (DS) from ultra-violet (UV)/visible (VIS) light to near infra-red (NIR) radiation in Nd{sup 3+} doped YBO{sub 3} and LaBO{sub 3} phosphors is reported. The prepared materials were characterized by X-ray powder diffraction (XRD) and photoluminescence (PL) properties along with time-decay curves were studied which confirmed the spectral DS from VIS to NIR radiation. This can be employed to overcome the spectral mismatch of crystalline silicon (c-Si) solar cell with solar spectrum. The prepared Nd{sup 3+} doped as prepared phosphors provide NIR emission (1052 nm) at excitation of 586 nm where response of c-Si solar cell was optimum. Thus spectral modification by mentioned phosphor can be utilized to improve solar cells performance. Hence these phosphors have potential application for photovoltaic (PV) technology. (orig.)

Photoluminescence characteristics of Sm{sup 3+} doped Ba{sub 3}La(PO{sub 4}){sub 3} as new orange-red emitting phosphors

Energy Technology Data Exchange (ETDEWEB)

Yu, Ruijin [College of Science, Northwest A and F University, Yangling, Shaanxi 712100 (China); Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Mi Noh, Hyeon; Kee Moon, Byung; Chun Choi, Byung [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Hyun Jeong, Jung, E-mail: jhjeong@pknu.ac.kr [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Sueb Lee, Ho [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jang, Kiwan, E-mail: kwjang@changwon.ac.kr [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Soo Yi, Soung [Department of Electronic Material Engineering, Silla University, Busan 617-736 (Korea, Republic of)

2014-01-15

A series of orange-red emitting Ba{sub 3}La(PO{sub 4}){sub 3}:xSm{sup 3+} (0.01≤x≤0.30) phosphors was synthesized by the convenient solid-state reaction. X-ray diffraction and photoluminescence spectra were utilized to characterize the structure and luminescence properties of the as-synthesized phosphors. The emission spectra of the Ba{sub 3}La(PO{sub 4}){sub 3}:Sm{sup 3+} phosphors consisted of some sharp emission peaks of Sm{sup 3+} ions centered at 563 nm, 600 nm, 647 nm, 710 nm. The strongest one is located at 600 nm due to {sup 4}G{sub 5/2}–{sup 6}H{sub 7/2} transition of Sm{sup 3+}, generating bright orange-red light. The optimum dopant concentration of Sm{sup 3+} ions in Ba{sub 3}La(PO{sub 4}):xSm{sup 3+} is around 5 mol% and the critical transfer distance of Sm{sup 3+} is calculated as 22 Å. The CIE chromaticity coordinates of the Ba{sub 3}La(PO{sub 4}){sub 3}:0.05Sm{sup 3+} phosphors was is located in the orange reddish region. The Ba{sub 3}La(PO{sub 4}){sub 3}:Sm{sup 3+} phosphors may be potentially used as red phosphors for white light-emitting diodes. -- Highlights: • A new Sm{sup 3+}-doped Ba{sub 3}La(PO{sub 4}){sub 3} phosphor was firstly synthesized. • Its structure, luminescent properties are well studied and characterized. • The Ba{sub 3}La(PO{sub 4}){sub 3}:Sm{sup 3+} shows bright orange reddish emissions under UV excitation.

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)

Tunable emission and the systematic study on energy-transfer properties of Ce3+- and Tb3+-co-doped Sr3(PO4)2 phosphors

International Nuclear Information System (INIS)

Liu, Zhijun

2015-01-01

An emitting color tunable phosphor Sr 3 (PO 4 ) 2 :Ce 3+ , Tb 3+ was synthesized by the traditional high-temperature solid-state reaction method. The photoluminescence and energy-transfer (ET) properties of Ce 3+ - and Tb 3+ -doped Sr 3 (PO 4 ) 2 host were studied in detail. The obtained phosphors show both a blue emission from Ce 3+ and a yellowish green emission from Tb 3+ with considerable intensity under ultraviolet (UV) excitation (∝311 nm). When the content of Ce 3+ was fixed at 0.03, the emission chromaticity coordinates could be adjusted from blue to green region by tuning the contents of Tb 3+ ions with the aid of ET process. The critical distance between Ce 3+ and Tb 3+ is 14.69 A. The ET mechanism from Ce 3+ to Tb 3+ ions was identified with dipole-dipole interaction. The obtained phosphor exhibits a strong excitation in UV spectral region and high-efficient ET from Ce 3+ to Tb 3+ ions. It may find applications as a green light-emitting UV-convertible phosphor in white LED devices. (orig.)

Optical properties of highly n-doped germanium obtained by in situ doping and laser annealing

Science.gov (United States)

Frigerio, J.; Ballabio, A.; Gallacher, K.; Giliberti, V.; Baldassarre, L.; Millar, R.; Milazzo, R.; Maiolo, L.; Minotti, A.; Bottegoni, F.; Biagioni, P.; Paul, D.; Ortolani, M.; Pecora, A.; Napolitani, E.; Isella, G.

2017-11-01

High n-type doping in germanium is essential for many electronic and optoelectronic applications especially for high performance Ohmic contacts, lasing and mid-infrared plasmonics. We report on the combination of in situ doping and excimer laser annealing to improve the activation of phosphorous in germanium. An activated n-doping concentration of 8.8  ×  1019 cm-3 has been achieved starting from an incorporated phosphorous concentration of 1.1  ×  1020 cm-3. Infrared reflectivity data fitted with a multi-layer Drude model indicate good uniformity over a 350 nm thick layer. Photoluminescence demonstrates clear bandgap narrowing and an increased ratio of direct to indirect bandgap emission confirming the high doping densities achieved.

Photoluminescence characteristics of Sm{sup 3+}-doped Ba{sub 2}CaWO{sub 6} as new orange–red emitting phosphors

Energy Technology Data Exchange (ETDEWEB)

Yu, Ruiijn [College of Science, Northwest A and F University, Yangling, Shaanxi 712100 (China); Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Mi Noh, Hyeon; Kee Moon, Byung; Chun Choi, Byung [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Hyun Jeong, Jung, E-mail: jhjeong@pknu.ac.kr [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of); Sueb Lee, Ho [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jang, Kiwan, E-mail: kwjang@changwon.ac.kr [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Soo Yi, Soung [Department of Electronic Material Engineering, Silla University, Busan 617-736 (Korea, Republic of)

2014-08-01

The orange–red emitting Ba{sub 2}CaWO{sub 6}:xSm{sup 3+} (0.01≤x≤0.25) phosphors were synthesized via solid state reaction process. The crystal structure of the phosphor was characterized by XRD. The photoluminescence excitation and emission spectra, concentration effect were investigated. The results show an efficient energy transfer from WO{sub 6}{sup 6−} group to Sm{sup 3+} occurs. The emission spectra of the Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} phosphors consisted of some sharp emission peaks of Sm{sup 3+} ions centre at 579 nm, 618 nm, 625 nm, and 675 nm. The strongest one is located at 610 nm due to {sup 4}G{sub 5/2}→{sup 6}H{sub 7/2} transition of Sm{sup 3+}, generating bright orange–red light. The optimum dopant concentration of Sm{sup 3+} ions in Ba{sub 2}CaWO{sub 6}:xSm{sup 3+} is around 5 mol% and the critical transfer distance of Sm{sup 3+} is calculated as 18 Å. The fluorescence lifetime of Sm{sup 3+} in Ba{sub 2}CaWO{sub 6}:0.05Sm{sup 3+} is 2.36 ms. The Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} phosphors may be potentially used as orange–red phosphors for white light-emitting diodes. - Highlights: • A new host-sensitized Sm{sup 3+}-doped Ba{sub 2}CaWO{sub 6} phosphor was firstly synthesized. • Its structure, luminescent properties are well studied and characterized. • There exists an efficient energy transfer from WO{sub 6}{sup 6−} group to Sm{sup 3+}. • The thermal quenching properties of Ba{sub 2}CaWO{sub 6}:Sm{sup 3+} was firstly evaluated.

A single-phase white light emitting Pr3+ doped Ba2CaWO6 phosphor: synthesis, photoluminescence and optical properties

Science.gov (United States)

Sreeja, E.; Vidyadharan, Viji; Jose, Saritha K.; George, Anns; Joseph, Cyriac; Unnikrishnan, N. V.; Biju, P. R.

2018-04-01

Pr3+ doped Ba2CaWO6 phosphor were prepared by traditional high-temperature solid-state reaction technique. The structure evolution was systematically investigated by X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) analysis. The X-ray powder diffraction patterns indicate that the prepared phosphors crystallized in the cubic double-perovskite structure. The functional groups were identified using FTIR spectra and the elements present in the composition were confirmed by the EDS profile. The morphology of the phosphor was identified using SEM and TEM analysis. The PL spectra illustrated that these phosphors could be efficiently excited by charge transfer band of host and the maximum luminescence intensity was observed at 0.06 wt% of Pr3+ ion. Upon the charge transfer band excitation, emission spectra showed peaks at 489, 532, 647, 685 and 737 nm corresponding to 3P0→3H4, 3P1→3H5, 3P0→3F2, 3P0→3F3 and 3P0→3F4 transitions respectively. The concentration quenching of Ba2CaWO6:Pr3+ phosphor can be mainly attributed to dipole-dipole interaction. The CIE coordinates were estimated to be close to the white region. The decay curves are well fitted with double exponential decay models. The standard and modified Judd-Ofelt (JO) theories were used to determine the Judd-Ofelt intensity parameters, radiative transition probabilities and branching ratios. The optical properties indicate that Ba2CaWO6:Pr3+ phosphors can produce white light emission from a single phase host and its potential application for solid-state lighting and display devices.

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.

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

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

Structure, luminescence and thermal quenching properties of Eu doped Sr{sub 2−x}Ba{sub x}Si{sub 5}N{sub 8} red phosphors

Energy Technology Data Exchange (ETDEWEB)

Liu, Y.H.; Chen, L.; Zhou, X.F.; Liu, R.H., E-mail: griremlrh@126.com; Zhuang, W.D.

2017-02-15

Eu{sup 2+} doped Sr{sub 2-x}Ba{sub x}Si{sub 5}N{sub 8} phosphors were synthesized at 1610 ℃ for 4 h via the solid-state reaction method. The XRD results confirm that the complete solid solutions are formed. With the increase of x, the emission spectra show an obvious blue-shift from 610 nm to 585 nm under the excitation of 460 nm. The color tone can be tuned from yellow to red. The corresponding mechanism for the blue-shift of peak-wavelength is studied in detail. The results of decomposed Gaussian spectra and fluorescence lifetime show that the local coordination structure surrounding activator ions changes with increasing x value. It is found that the probability of Eu occupying Sr1 and Sr2 site is dependent on Ba/Sr ratio. The variation of thermal quenching properties and the corresponding mechanism is discussed in detail. The results indicate that Eu{sup 2+} doped Sr{sub 2-x}Ba{sub x}Si{sub 5}N{sub 8} is a promising orange red-emitting phosphor for near UV or blue light-pumped white light-emitting-diodes (wLEDs). - Graphical abstract: Eu{sup 2+} doped Sr{sub 2-x}Ba{sub x}Si{sub 5}N{sub 8} solid solutions were prepared by the solid-state reaction method. The structure, luminescence and thermal quenching properties with varying Ba/Sr ratio were investigated in detail. - Highlights: • The stucture and luminescence properties of Eu doped Sr{sub 2-x}Ba{sub x}Si{sub 5}N{sub 8} phosphors were investigated. • The samples with the intermediate compositions(x=1.0,1.5) show better stability than the end members of both Sr{sub 2}Si{sub 5}N{sub 8}:Eu{sup 2+} and Ba{sub 2}Si{sub 5}N{sub 8}:Eu{sup 2+}. • The possible mechanism for the improvement of thermal quenching properties was proposed.

Mechanoluminescence, photoluminescence and thermoluminescence studies of SrZrO3:Ce phosphor

Directory of Open Access Journals (Sweden)

Neha Tiwari

2015-01-01

Full Text Available The present paper reports the synthesis and characterization, photoluminescence thermoluminescence and mechanoluminescence studies of Ce3+ doped SrZrO3 phosphors. The effects of variable concentration of Cerium on meachanoluminescence (ML and photoluminescence behavior were studied. The samples were prepared by combustion a synthesis technique which is suitable for less time taking techniques also for large scale production for phosphors. The starting material used for sample preparation are Sr(NO33, Zr(NO33 XH2O and Ce(NO33 6H2O and urea used as a fuel. The prepared sample was characterized by X-ray diffraction technique (XRD with variable concentration of Ce (0.05–0.5 mol%. There is no any phase change found with increase the concentration of Ce. Sample shows orthorhombic structure and the particle size calculated by Scherer's formula. The surface morphology of prepared phosphor was determined by field emission gun scanning electron microscopy (FEGSEM technique. Mechanoluminescence studies on SrZrO3phosphors doped with Ce and underwent an impulsive deformation with an impact of a piston for Mechanoluminescence (ML investigations. Temporal characteristics in order to investigate about the luminescence centre responsible for ML peak, increasing impact velocity causes more number of electrons will be ionized to reach to the conduction band so there will be more number of electrons available to be recombined at recombination or luminescence centre. In photoluminescence study PL emission spectra show the isolated peak position observed at 388 nm near UV region of spectrum due to 5d–4f transition of Ce3+ion.Thermoluminescence study shows doping of Ce3+ ions reduced the TL intensity TL glow curve shows the high fading and less stability when it doped with cerium. The activation energy high for the doped SrZrO3 phosphor means that the trapped electron is highly trapped in trap level. The present study gives the advance application for fracture

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)

Adjusting White OLEDs with Yellow Light Emission Phosphor Dye and Ultrathin NPB Layer Structure

Directory of Open Access Journals (Sweden)

Jun Wang

2013-01-01

Full Text Available High efficiency white organic light emission devices were demonstrated with phosphor material dye bis[2-(4-tertbutylphenylbenzothiazolato-N,C2′]iridium (acetylacetonate and ultrathin layer structure. The ultra thin layer be composed of 4,4′-bis[N-1-naphthyl-N-phenyl-amino]biphenyl (NPB or 4,4′-N,N′-dicarbazole-biphenyl : NPB mixed layer with blue light emission. The emission spectra of devices could be adjusted by different phosphor doping concentrations and ultra thin layer structure. Warm white light emitting device could be obtained with 5 wt% doping concentration and power efficiency of 9.93 lm/W at 5 V. Pure white light with Commission Internationale de l'Eclairage (CIE coordinates of (0.33, 0.30 and external quantum efficiency of 4.49% could be achieved with ultra thin layer device structure and 3 wt% phosphor doped device.

New NaSrPO4:Sm phosphor as orange-red emitting material

Indian Academy of Sciences (India)

Because NaSr1−xPO4:xSm3+ phosphor features a high colour-rendering index and chemical stability, it is potentially ... use blue LED chips (GaN or InGaN) with a yellow phosphor ... excitation by doping Sm3+ rare earth ions into a suitable.

Luminescent properties of (Y,Gd)BO3:Bi3+,RE3+ (RE=Eu, Tb) phosphor under VUV/UV excitation

International Nuclear Information System (INIS)

Zeng Xiaoqing; Im, Seoung-Jae; Jang, Sang-Hun; Kim, Young-Mo; Park, Hyoung-Bin; Son, Seung-Hyun; Hatanaka, Hidekazu; Kim, Gi-Young; Kim, Seul-Gi

2006-01-01

Bi 3+ - and RE 3+ -co-doped (Y,Gd)BO 3 phosphors were prepared and their luminescent properties under vacuum ultraviolet (VUV)/UV excitation were investigated. Strong red emission for (Y,Gd)BO 3 :Bi 3+ ,Eu 3+ and strong green emission for (Y,Gd)BO 3 :Bi 3+ ,Tb 3+ are observed under VUV excitation from 147 to 200 nm with a much broader excitation region than that of single Eu 3+ -doped or Tb 3+ -doped (Y,Gd)BO 3 phosphor. Strong emissions are also observed under UV excitation around 265 nm where as nearly no luminescence is observed for single Eu 3+ -doped or Tb 3+ -doped (Y,Gd)BO 3 . The luminescence enhancement of Bi 3+ - and RE 3+ -co-doped (Y,Gd)BO 3 phosphors is due to energy transfer from Bi 3+ ion to Eu 3+ or Tb 3+ ion not only in the VUV region but also in the UV region. Besides, host sensitization competition between Bi 3+ and Eu 3+ or Tb 3+ is also observed. The investigated phosphors may be preferable for devices with a VUV light 147-200 nm as an excitation source such as PDP or mercury-free fluorescent lamp

Photoluminescence properties and energy transfer in Ce(3+) /Dy(3+) co-doped Sr(3) MgSi(2) O(8) phosphors for potential application in ultraviolet white light-emitting diodes.

Science.gov (United States)

Yu, Hong; Zi, Wenwen; Lan, Shi; Gan, Shucai; Zou, Haifeng; Xu, Xuechun; Hong, Guangyan

2013-01-01

Sr(3) MgSi(2) O(8) :Ce(3+) , Dy(3+) phosphors were prepared by a solid-state reaction technique and the photoluminescence properties were investigated. The emission spectra show not only a band due to Ce(3+) ions (403 nm) but also as a band due to Dy(3+) ions (480, 575 nm) (UV light excitation). The photoluminescence properties reveal that effective energy transfer occurs in Ce(3+) /Dy(3+) co-doped Sr(3) MgSi(2) O(8)phosphors, and the co-doping of Ce(3+) could enhance the emission intensity of Dy(3+) to a certain extent by transferring its energy to Dy(3+) . The Ce(3+) /Dy(3+) energy transfer was investigated by emission/excitation spectra, and photoluminescence decay behaviors. In Sr2.94 MgSi2 O8 :0.01Ce(3+) , 0.05Dy(3+) phosphors, the fluorescence lifetime of Dy(3+) (from 3.35 to 27.59 ns) is increased whereas that of Ce(3+) is greatly decreased (from 43.59 to 13.55 ns), and this provides indirect evidence of the Ce(3+) to Dy(3+) energy transfer. The varied emitted color of Sr(3) MgSi(2) O(8):Ce(3+) , Dy(3+) phosphors from blue to white were achieved by altering the concentration ratio of Ce(3+) and Dy(3+) . These results indicate Sr(3) MgSi(2) O(8):Ce(3+) , Dy(3+) may be as a candidate phosphor for white light-emitting diodes. Copyright © 2012 John Wiley & Sons, Ltd.

Red emitting phosphors of Eu3+ doped Na2Ln2Ti3O10 (Ln = Gd, Y) for white light emitting diodes

International Nuclear Information System (INIS)

Zhang, Niumiao; Guo, Chongfeng; Yin, Luqiao; Zhang, Jianhua; Wu, Mingmei

2015-01-01

Highlights: • Layered red phosphors Na 2 Ln 2 Ti 3 O 10 (Ln = Gd, Y):Eu 3+ were prepared. • The synthesis parameters of phosphors were optimized. • PL and thermal stability of the samples were investigated. • LED devices were also fabricated including the present red phosphor. - Abstract: A series of Eu 3+ doped Na 2 Ln 2 Ti 3 O 10 (Ln = Gd, Y) red-emitting phosphors for application in ultraviolet based light emitting diodes (LEDs) were successfully synthesized by a modified sol–gel method. Their structure and luminescent properties were characterized by powder X-ray diffraction (XRD), photoluminescence excitation (PLE) and emission (PL) spectra and absorption spectra, according to these results the optimal compositions and synthesis parameters were determined. In addition, the thermal stabilities of the phosphors were investigated according to the temperature-dependent PL spectra. The red and white-LEDs (W-LEDs) comprising the Na 2 Ln 2 Ti 3 O 10 :Eu 3+ (Ln = Gd, Y) red emitting phosphors were fabricated with a near-ultraviolet (n-UV) chip. In comparison with Na 2 Y 1.4 Eu 0.6 Ti 3 O 10 , the Na 2 Gd 0.6 Eu 1.4 Ti 3 O 10 phosphor offers higher brightness, quantum efficiency, and excellent thermal stability. W-LEDs comprising Na 2 Gd 0.6 Eu 1.4 Ti 3 O 10 showed bright white emission with a color rendering index (Ra) of 82, a color temperature of 2151 K, and Commission Internationale de I’Eclairage (CIE) color coordinates of (0.34, 0.37). The phosphor Na 2 Gd 0.6 Eu 1.4 Ti 3 O 10 is more suitable candidate for application in LEDs

Enhancement of the mechanoluminescence properties on Ca2MgSi2O7:Dy3+ phosphor by co-doping of charge compensator ions

Science.gov (United States)

Sahu, Ishwar Prasad

2016-08-01

In the present article, effect of charge compensator ions (R+ = Li+, Na+ and K+) on dysprosium-doped di-calcium magnesium di-silicate (Ca2MgSi2O7:Dy3+) phosphors were investigated. The Ca2MgSi2O7:Dy3+ and Ca2MgSi2O7:Dy3+, R+ phosphors, were prepared by solid-state reaction method. The crystal structures of sintered phosphors were an akermanite-type structure which belongs to the tetragonal crystallography. The peaks of mechanoluminescence (ML) intensity were increased linearly with increasing impact velocity of the moving piston. Thus, present investigation indicates that the piezoelectricity was responsible to produce ML in prepared phosphors. The time of the peak ML intensity and the decay rate did not change significantly with respect to increasing impact velocity. Addition of charge compensator ions enhances the luminescence intensity of prepared Ca2MgSi2O7:Dy3+ phosphors, because they neutralize the charge generated by Dy3+ substitution for Ca2+ ions. The role of Li+ ions among all charge compensator ions (Na+ or K+) used was found to be most effective for enhanced Dy3+ ion emission. These ML materials can be used in the devices such as stress sensor, fracture sensor, impact sensor, damage sensors, safety management monitoring system and fuse system for army warheads.

Eu and Sr2CeO4 : Eu phosphors suitable for near ultraviolet excitation

Indian Academy of Sciences (India)

Administrator

The study on white light phosphors suitable for near- ultraviolet (nUV) ... Rare earth ion-doped phosphors have been used in varied fields ... practical applications. .... by naked eyes. ... induced by Sr2CeO4 host matrix (Arunachalam Laxmanan.

Combustion synthesis of Eu and Dy activated Sr3(VO4)2 phosphor ...

Indian Academy of Sciences (India)

phosphor as well as Sr3(VO4)2:Dy is blue and yellow emitting phosphor for solid state lighting i.e. white LEDs. The ... 2004; Pang et al 2004) doped with rare earth has expanded ... controlled since the LED light output (intensity and colour).

Investigation of saturation effects in ceramic phosphors for laser lighting

DEFF Research Database (Denmark)

Krasnoshchoka, Anastasiia; Thorseth, Anders; Dam-Hansen, Carsten

2017-01-01

We report observation of saturation effects in a Ce:LuAG and Eu-doped nitride ceramic phosphor for conversion of blue laser light for white light generation. The luminous flux from the phosphors material increases linearly with the input power until saturation effects limit the conversion....... It is shown, that the temperature of the phosphor layer influences the saturation power level and the conversion efficiency. It is also shown that the correlated color temperature (CCT), phosphor conversion efficiency and color rendering index (CRI) are dependent both on incident power and spot size diameter...... of the illumination. A phosphor conversion efficiency up to 140.8 lm/W with CRI of 89.4 was achieved. The saturation in a ceramic phosphor, when illuminated by high intensity laser diodes, is estimated to play the main role in limiting the available luminance from laser based lighting systems....

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

Optical properties of highly n-doped germanium obtained by in situ doping and laser annealing

International Nuclear Information System (INIS)

Frigerio, J; Ballabio, A; Isella, G; Gallacher, K; Millar, R; Paul, D; Gilberti, V; Baldassarre, L; Ortolani, M; Milazzo, R; Napolitani, E; Maiolo, L; Minotti, A; Pecora, A; Bottegoni, F; Biagioni, P

2017-01-01

High n-type doping in germanium is essential for many electronic and optoelectronic applications especially for high performance Ohmic contacts, lasing and mid-infrared plasmonics. We report on the combination of in situ doping and excimer laser annealing to improve the activation of phosphorous in germanium. An activated n-doping concentration of 8.8  ×  10 19 cm −3 has been achieved starting from an incorporated phosphorous concentration of 1.1  ×  10 20 cm −3 . Infrared reflectivity data fitted with a multi-layer Drude model indicate good uniformity over a 350 nm thick layer. Photoluminescence demonstrates clear bandgap narrowing and an increased ratio of direct to indirect bandgap emission confirming the high doping densities achieved. (paper)

Dielectric loss property of strong acids doped polyaniline (PANi)

Science.gov (United States)

Amalia, Rianti; Hafizah, Mas Ayu Elita; Andreas, Manaf, Azwar

2018-04-01

In this study, strong acid doped polyaniline (PANi) has been successfully fabricated through the chemical oxidative polymerization process with various polymerization times. Nonconducting PANi resulting from the polymerization process at various polymerization times were then doped by a strong acid HClO4 to generate dielectric properties. Ammonium Persulfate (APS) as an initiator was used during Polymerization process to develop dark green precipitates which then called Emeraldine Base Polyaniline (PANi-EB). The PANi-EB was successively doped by strong acid HClO4 with dopant and PANi ratio 10:1 to enhance the electrical conductivity. The conductivity of doped PANi was evaluated by Four Point Probe. Results of evaluation showed that the conductivity values of HClO4 doped PANi were in the range 337-363 mS/cm. The dielectric properties of doped PANi were evaluated by Vector Network Analyzer (VNA) which suggested that an increase in the permittivity value in the conducting PANi. It is concluded that PANi could be a potential candidate for electromagnetic waves absorbing materials.

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.

Luminescence characteristic of YVO{sub 4}:Eu{sup 3+} thin film phosphors by Li doping

Energy Technology Data Exchange (ETDEWEB)

Yang, Hyun Kyoung; Shim, Kyoo Sung; Moon, Byung Kee; Choi, Byung Chun [Department of Physics, Pukyong National University, Busan 608-737, Republic Korea (Korea, Republic of); Jeong, Jung Hyun [Department of Physics, Pukyong National University, Busan 608-737, Republic Korea (Korea, Republic of)], E-mail: jhjeong@pknu.ac.kr; Yi, Soung Soo [Department of Electronic Materials Engineering, Silla University, Busan 608-736, Republic Korea (Korea, Republic of); Kim, Jung Hwan [Department of Physics, Dong Eui University, Busan 614-714, Republic Korea (Korea, Republic of)

2008-06-30

YVO{sub 4}:Eu{sup 3+} and Li-doped YVO{sub 4}:Eu{sup 3+} thin film phosphors have been deposited on Al{sub 2}O{sub 3} (0001) substrate using a pulsed laser deposition technique. The Li{sup +} ions concentration was varied from 0 to 3 wt.% and Li{sup +} doping influenced crystallinity and surface morphology of YVO{sub 4}:Eu{sup 3+} films.. As Li{sup +} content increases from 0 wt.% to 2 wt.%, not only crystallinity was improved, but also the shape of grains was rounded. However, Li{sup +} content, increases further to 3 wt.% the shape of grains was changed to elliptical. The emitted radiation was dominated by a red emission peak at 619 nm radiated from the {sup 5}D{sub 0}-{sup 7}F{sub 2} transition of Eu{sup 3+} ions. In particular, the incorporation of Li{sup +} ions into YVO{sub 4} lattice could induce an increase of photoluminescence. The enhanced luminescence results not only from the improved crystallinity but also from the enhanced surface roughness. The luminescent intensity and surface roughness exhibited similar behavior as a function of Li{sup +} ions concentration.

Transition of Emission Colours as a Consequence of Heat-Treatment of Carbon Coated Ce3+-Doped YAG Phosphors

Directory of Open Access Journals (Sweden)

Liang-Jun Yin

2017-10-01

Full Text Available To modify the luminescence properties of Ce3+-doped Y3Al5O12 (YAG phosphors, they have been coated with a carbon layer by chemical vapor deposition and subsequently heat-treated at high temperature under N2 atmosphere. Luminescence of the carbon coated YAG:Ce3+ phosphors has been investigated as a function of heat-treatment at 1500 and 1650 °C. The 540 nm emission intensity of C@YAG:Ce3+ is the highest when heated at 1650 °C, while a blue emission at 400–420 nm is observed when heated at 1500 °C but not at 1650 °C. It is verified by X-ray diffraction (XRD that the intriguing luminescence changes are induced by the formation of new phases in C@YAG:Ce3+-1500 °C, which disappear in C@YAG:Ce3+-1650 °C. In order to understand the mechanisms responsible for the enhancement of YAG:Ce3+ emission and the presence of the blue emission observed for C@YAG:Ce3+-1500 °C, the samples have been investigated by a combination of several electron microscopy techniques, such as HRTEM, SEM-CL, and SEM-EDS. This local and cross-sectional analysis clearly reveals a gradual transformation of phase and morphology in heated C@YAG:Ce3+ phosphors, which is related to a reaction between C and YAG:Ce3+ in N2 atmosphere. Through reaction between the carbon layer and YAG host materials, the emission colour of the phosphors can be modified from yellow, white, and then back to yellow under UV excitation as a function of heat-treatment in N2 atmosphere.

Transition of Emission Colours as a Consequence of Heat-Treatment of Carbon Coated Ce3+-Doped YAG Phosphors.

Science.gov (United States)

Yin, Liang-Jun; Dierre, Benjamin; Sekiguchi, Takashi; van Ommen, J Ruud; Hintzen, Hubertus T Bert; Cho, Yujin

2017-10-16

To modify the luminescence properties of Ce 3+ -doped Y₃Al₅O 12 (YAG) phosphors, they have been coated with a carbon layer by chemical vapor deposition and subsequently heat-treated at high temperature under N₂ atmosphere. Luminescence of the carbon coated YAG:Ce 3+ phosphors has been investigated as a function of heat-treatment at 1500 and 1650 °C. The 540 nm emission intensity of C@YAG:Ce 3+ is the highest when heated at 1650 °C, while a blue emission at 400-420 nm is observed when heated at 1500 °C but not at 1650 °C. It is verified by X-ray diffraction (XRD) that the intriguing luminescence changes are induced by the formation of new phases in C@YAG:Ce 3+ -1500 °C, which disappear in C@YAG:Ce 3+ -1650 °C. In order to understand the mechanisms responsible for the enhancement of YAG:Ce 3+ emission and the presence of the blue emission observed for C@YAG:Ce 3+ -1500 °C, the samples have been investigated by a combination of several electron microscopy techniques, such as HRTEM, SEM-CL, and SEM-EDS. This local and cross-sectional analysis clearly reveals a gradual transformation of phase and morphology in heated C@YAG:Ce 3+ phosphors, which is related to a reaction between C and YAG:Ce 3+ in N₂ atmosphere. Through reaction between the carbon layer and YAG host materials, the emission colour of the phosphors can be modified from yellow, white, and then back to yellow under UV excitation as a function of heat-treatment in N₂ atmosphere.

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)

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...

Infrared emissions in MgSrAl10O17:Er3+ phosphor co-doped with Yb3+/Ba2+/Ca2+ obtained by solution combustion route

International Nuclear Information System (INIS)

Singh, Vijay; Kumar Rai, Vineet; Venkatramu, V.; Chakradhar, R.P.S.; Hwan Kim, Sang

2013-01-01

An intense infrared emitting MgSrAl 10 O 17 :Er 3+ phosphor co-doped with Yb 3+ , Ba 2+ and Ca 2+ ions have been prepared by a solution combustion method. Phase purity of the derived compounds was confirmed by X-ray diffraction technique. The vibrational properties of MgSrAl 10 O 17 phosphor was studied by Fourier transform infrared spectroscopy. The broad and strong infrared emission of Er 3+ ions at around 1.53 μm was observed upon excitation at 980 nm. Effect of co-doping with the Yb 3+ , Ba 2+ and Ca 2+ ions on the infrared luminescence intensity of Er 3+ ions and the mechanism responsible for the variation in the infrared intensity have been discussed. The results indicate that these materials may be suitable for the optical telecommunication window and wavelength division multiplexing applications. - Highlights: ► The hexagonal phase of MgSrAl 10 O 17 could be obtained by the low temperature combustion method. ► The broad and strong infrared emission of Er 3+ ions at around 1.53 μm was observed. ► Effect of co-doping with the Yb 3+ , Ba 2+ and Ca 2+ ions on the infrared luminescence intensity of Er 3+ were reported.

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

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.

Catalyst Degradation in High Temperature Proton Exchange Membrane Fuel Cells Based on Acid Doped Polybenzimidazole Membranes

DEFF Research Database (Denmark)

Cleemann, Lars Nilausen; Buazar, F.; Li, Qingfeng

2013-01-01

and multi‐walled carbon nanotubes were used as supports for electrode catalysts and evaluated in accelerated durability tests under potential cycling at 150 °C. Measurements of open circuit voltage, area specific resistance and hydrogen permeation through the membrane were carried out, indicating little...... contribution of the membrane degradation to the performance losses during the potential cycling tests. As the major mechanism of the fuel cell performance degradation, the electrochemical active area of the cathodic catalysts showed a steady decrease in the cyclic voltammetric measurements, which was also......Degradation of carbon supported platinum catalysts is a major failure mode for the long term durability of high temperature proton exchange membrane fuel cells based on phosphoric acid doped polybenzimidazole membranes. With Vulcan carbon black as a reference, thermally treated carbon black...

High-Throughput Synthesis and Characterization of Eu Doped Ba xSr2- xSiO4 Thin Film Phosphors.

Science.gov (United States)

Frost, Sara; Guérin, Samuel; Hayden, Brian E; Soulié, Jean-Philippe; Vian, Chris

2018-06-20

High-throughput techniques have been employed for the synthesis and characterization of thin film phosphors of Eu-doped Ba x Sr 2- x SiO 4 . Direct synthesis from evaporation of the constituent elements under a flux of atomic oxygen on a sapphire substrate at 850 °C was used to directly produce thin film libraries (415 nm thickness) of the crystalline orthosilicate phase with the desired compositional variation (0.24 > x > 1.86). The orthosilicate phase could be synthesized as a pure, or predominantly pure, phase. Annealing the as synthesized library in a reducing atmosphere resulted in the reduction of the Eu while retaining the orthosilicate phase, and resulted in a materials thin film library where fluorescence excited by blue light (450 nm) was observable by the naked eye. Parallel screening of the fluorescence from the combinatorial libraries of Eu doped Ba x Sr 2- x SiO 4 has been implemented by imaging the fluorescent radiation over the library using a monochrome digital camera using a series of color filters. Informatics tools have been developed to allow the 1931 CIE color coordinates and the relative quantum efficiencies of the materials library to be rapidly assessed and mapped against composition, crystal structure and phase purity. The range of compositions gave values of CIE x between 0.17 and 0.52 and CIE y between 0.48 and 0.69 with relative efficiencies in the range 2.0 × 10 -4 -7.6 × 10 -4 . Good agreement was obtained between the thin film phosphors and the fluorescence characteristics of a number of corresponding bulk phosphor powders. The thermal quenching of fluorescence in the thin film libraries was also measured in the temperature range 25-130 °C: The phase purity of the thin film was found to significantly influence both the relative quantum efficiency and the thermal quenching of the fluorescence.

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.

Ultraviolet /UV/ sensitive phosphors for silicon imaging detectors

Science.gov (United States)

Viehmann, W.; Cowens, M. W.; Butner, C. L.

1981-01-01

The fluorescence properties of UV sensitive organic phosphors and the radiometric properties of phosphor coated silicon detectors in the VUV, UV, and visible wavelengths are described. With evaporated films of coronene and liumogen, effective quantum efficiencies of up to 20% have been achieved on silicon photodiodes in the vacuum UV. With thin films of methylmethacrylate (acrylic), which are doped with organic laser dyes and deposited from solution, detector quantum efficiencies of the order of 15% for wavelengths of 120-165 nm and of 40% for wavelengths above 190 nm have been obtained. The phosphor coatings also act as antireflection coatings and thereby enhance the response of coated devices throughout the visible and near IR.

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.

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

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.

Eu2+-doped Ba2GaB4O9Cl blue-emitting phosphor with high color purity for near-UV-pumped white light-emitting diodes

Science.gov (United States)

Gao, Zhiwen; Deng, Huajuan; Xue, Na; Jeong, Jung Hyun; Yu, Ruijin

2018-01-01

Eu2+-doped borate fluoride Ba2GaB4O9Cl was synthesized by the conventional high-temperature solid-state reaction. The crystal structure and luminescence properties of the phosphors, as well as their thermal luminescence quenching capabilities and CIE chromaticity coordinates were systematically investigated. Under the excitation at 340 nm, the phosphor exhibited an asymmetric broad-band blue emission with a peak at 445 nm, which is ascribed to the 4f-5d transition of Eu2+. It was further proved that energy transfer among the nearest neighbor ions is the major mechanism for concentration quenching of Eu2+ in Ba2-xGaB4O9Cl:xEu2+ phosphors. The luminescence quenching temperature is 432 K. The CIE color coordinates are very close to those of BaMgAl10O17:Eu2+ (BAM). All the properties indicated that the blue-emitting Ba2GaB4O9Cl:Eu2+ phosphor has potential application in white LEDs.

Luminescence and electron degradation properties of Bi doped CaO phosphor

Energy Technology Data Exchange (ETDEWEB)

Yousif, A. [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Department of Physics, Faculty of Education, University of Khartoum, P.O. Box 321, 11115 Omdurman (Sudan); Kroon, R.E.; Coetsee, E.; Ntwaeaborwa, O.M. [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Seed Ahmed, H.A.A. [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa); Department of Physics, Faculty of Education, University of Khartoum, P.O. Box 321, 11115 Omdurman (Sudan); Swart, H.C., E-mail: swarthc@ufs.ac.za [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein, ZA 9300 (South Africa)

2015-11-30

Graphical abstract: - Highlights: • Blue emitting Ca{sub 1−x}O:Bi{sub x=0.5%} phosphor powder was successfully prepared. • Strong blue near-UV emission was obtained. • Electron beam induced cathodoluminescence intensity degradation occurred. • XPS was successfully used to explain the degradation process. - Abstract: Ca{sub 1−x}O:Bi{sub x=0.5%} phosphor powder was successfully synthesized by the sol-gel combustion method. The structure, morphology and luminescent properties of the phosphor were characterized by X-ray diffraction, scanning electron microscopy, photoluminescence and cathodoluminescence (CL) spectroscopy. The results showed that the Ca{sub 1−x}O:Bi{sub x=0.5%} consisted of single face-centred cubic crystals and that the phosphor particles were uniformly distributed. When the phosphor was excited by a xenon lamp at 355 nm, or a 325 nm He–Cd laser, or electron beam, it emitted strongly in the blue near-UV range with a wavelength of 395 nm ({sup 3}P{sub 1} → {sup 1}S{sub 0} transition of Bi{sup 3+}). The CL intensity was monitored as a function of the accelerating voltage and also as a function of the beam current. The powder was also subjected to a prolonged electron beam irradiation to study the electron beam induced CL intensity degradation. X-ray photoelectron spectroscopy was used to analyze the Ca{sub 1−x}O:Bi{sub x=0.5%} phosphor sample surface before and after degradation.

Study on preparation of orange-emitting phosphor Y3Mg2AlSi2O12: Ce3+ for wLED

Directory of Open Access Journals (Sweden)

Yan Shirun

2017-12-01

Full Text Available Ce3+-doped garnet-structured orange-emitting phosphor Y3Mg2AlSi2O12:Ce3+ was prepared by sol-gel combustion using urea as a fuel.Effects of the reduction temperature,Ce3+ doping concentration on the structure,morphology,and photoluminescence property of the as-prepared phosphor were investigated by X-ray diffraction(XRD,scaning electron microscope(SEM,photoluminescence spectroscopy and UV-Vis reflection spectroscopy.The crystallinities,morphologies,and photoluminescence properties of the phosphors prepared by sol-gel combustion and solid-state reaction were compared.The reasons causing different performance of the phosphors were discussed.

Surface and spectral studies of green emitting Sr{sub 3}B{sub 2}O{sub 6}:Tb{sup 3+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Neharika [School of Physics, Shri Mata Vaishno Devi University, Katra 182320, J& K (India); Kumar, Vinay, E-mail: vinaykumar@smvdu.ac.in [School of Physics, Shri Mata Vaishno Devi University, Katra 182320, J& K (India); Sharma, J.; Singh, Vivek K. [School of Physics, Shri Mata Vaishno Devi University, Katra 182320, J& K (India); Ntwaeaborwa, O.M.; Swart, H.C. [Department of Physics, University of the Free State, PO Box 339, Bloemfontein ZA9300 (South Africa)

2016-01-15

Highlights: • XPS technique has been used to study the surface composition of the phosphor. • The phosphor is synthesized by combustion method using urea as fuel. • Multipole–multipole interaction was found to play a key role for concentration quenching of Tb{sup 3+} doped Sr{sub 3}B{sub 2}O{sub 6} phosphor. - Abstract: In this paper, we report the synthesis of trivalent Tb{sup 3+} doped Sr{sub 3}B{sub 2}O{sub 6} phosphor by combustion method using urea as an organic fuel. The structure of the product has been verified by X-ray diffraction study which shows a rhombohedral phase with a space group of R-3c having lattice constants a = 9.064 Å, b = 9.064 Å, c = 12.611 Å. X-ray photoelectron spectroscopy has been used to study the elemental composition and electronic states of the Tb{sup 3+} doped Sr{sub 3}B{sub 2}O{sub 6} phosphor. Photoluminescence spectra showed that the phosphor emits in the greenish region (with the main peak at 544 nm) of color gamut under UV excitation. The diffuse reflectance spectra of the Sr{sub 3}B{sub 2}O{sub 6} phosphor were studied. Lifetime and band gap of the phosphors were calculated to be 2.55 ms and 5.25 ± 0.02 eV, respectively.

Study on luminescence characteristics of blue OLED with phosphor-doped host-guest structure

Science.gov (United States)

Wang, Zhen; Liu, Fei; Zheng, Xin; Chen, Ai; Xie, Jia-feng; Zhang, Wen-xia

2018-05-01

In this study, we design and fabricate phosphor-doped host-guest structure organic light-emitting diodes (OLEDs), where the blue-ray iridium complex electrophosphorescent material FIrpic acts as object material. Properties of the device can be accommodated by changing the host materials, dopant concentration and thickness of the light-emitting layer. The study shows that the host material N,N'-dicarbazolyl-3,5-benzene (mCP) has a higher triplet excited state energy level, which can effectively prevent FIrpic triplet excited state energy backtracking to host material, thus the luminous efficiency is improved. When mCP is selected as the host material, the thickness of the light-emitting layer is 30 nm and the dopant concentration is 8 wt%, the excitons can be effectively confined in the light-emitting region. As a result, the maximum current efficiency and the maximum brightness of the blue device can reach 15.5 cd/A and 7 196.3 cd/m2, respectively.

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)

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

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.

synthesis and optical characterization of acid-doped polyaniline thin

African Journals Online (AJOL)

HOD

SYNTHESIS AND OPTICAL CHARACTERIZATION OF ACID-DOPED. POLYANILINE THIN .... MATERIALS AND METHODS .... Characterization of Se Doped Polyaniline”,Current. Applied ... with Silver Nanoparticles”, Advances in Materials.

Hydrogenation of gold-related levels in silicon by electrolytic doping

International Nuclear Information System (INIS)

Pearton, S.J.; Hansen, W.L.; Haller, E.E.; Kahn, J.M.

1984-01-01

The deep gold-related donor and acceptor levels in silicon have been neutralized to several μm depth by introducing atomic hydrogen using an electrolytic method. Using phosphoric or sulfuric acid as the electrolyte, it is possible to dope the crystalline silicon with hydrogen at elevated temperatures (200--280 0 C) allowing direct comparison with other means of introduction, such as hydrogen plasma exposure. We find the electrolytic method is not as efficient as plasma treatment for the same conditions, possibly due to oxide formation during the immersion in the acid

Luminescence property and emission enhancement of YbAlO3:Mn4+ red phosphor by Mg2+ or Li+ ions

Science.gov (United States)

Cao, Renping; Luo, Wenjie; Xu, Haidong; Luo, Zhiyang; Hu, Qianglin; Fu, Ting; Peng, Dedong

2016-03-01

YbAlO3:Mn4+, YbAlO3:Mn4+, Li+, and YbAlO3:Mn4+, Mg2+ phosphors are synthesized by high temperature solid-state reaction method in air. Their crystal structures and luminescence properties are investigated. Photoluminescence excitation (PLE) spectrum monitored at 677 nm contains broad PLE band with three PLE peaks located at ∼318, 395, and 470 nm within the range 220-600 nm. Emission spectra with excitation 318 and 470 nm exhibit three emission band peaks located at ∼645, 677, and 700 nm in the range of 610-800 nm and their corresponding chromaticity coordinates are about (x = 0.6942, y = 0.3057). The possible luminous mechanism of Mn4+ ion is analyzed by the simple energy level diagram of Mn4+ ion. The optimum Mn4+-doped concentration in YbAlO3:Mn4+ phosphor is about 0.4 mol% and the luminescence lifetime of YbAlO3:0.4%Mn4+ phosphor is ∼0.59 ms. Emission intensity of YbAlO3:0.4%Mn4+ phosphor can be enhanced ∼6 times after Mg2+ ion is co-doped and it is ∼2 times when Li+ ion is co-doped. The content in the paper is useful to research new Mn4+-doped luminescence materials and improve luminescence property of other Mn4+-doped phosphors.

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)

Growth and characterization of KDP crystals doped with L-aspartic acid.

Science.gov (United States)

Krishnamurthy, R; Rajasekaran, R; Samuel, Bincy Susan

2013-03-01

Potassium Dihydrogen Phosphate (KDP) doped with L-aspartic acid has been grown by solvent slow evaporation technique from a mixture of aqueous solution of KDP and 0.7% of L-aspartic acid at room temperature. The grown crystals were characterized by powder X-ray diffraction, UV-visible, FTIR analysis. The doping of aspartic acid was confirmed by FTIR spectrum. The Nonlinear optical property (SHG) of L-aspartic acid doped KDP has been confirmed. Microhardness studies were carried out on the grown crystal. Copyright © 2012 Elsevier B.V. All rights reserved.

The effect of preparation method on the proton conductivity of indium doped tin pyrophosphates

DEFF Research Database (Denmark)

Anfimova, Tatiana; Lie-Andersen, T.; Jensen, E. Pristed

2015-01-01

Indium doped tin pyrophosphates were prepared by three synthetic routes. A heterogeneous synthesis from metal oxides with excess phosphoric acid produces crystalline phosphate particles with a phosphorus rich amorphous phase along the grain boundaries. The amorphous phase prevents the agglomeration...... decrease in conductivity as well as significant agglomeration of the particles, as evident in TEM and from particle size distribution measurements. Homogeneous synthesis with soluble metal acetates or chlorides as precursors results in a single crystalline phase with a small particle size, but strongly...... agglomerated, and a low conductivity at 10- 7-10- 6 Scm- 1 level. Further impregnation of the agglomerates with phosphoric acid does not lead to formation of the phosphorus rich amorphous layers on the surface of the crystals. An intermediate conductivity of 10- 3 Scm- 1 was observed for the acid treated...

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

Compact fluorescent lamp phosphors in accidental radiation monitoring

International Nuclear Information System (INIS)

Murthy, K. V. R.; Pallavi, S. P.; Ghildiyal, R.; Parmar, M. C.; Patel, Y. S.; Ravi Kumar, V.; Sai Prasad, A. S.; Natarajan, V.; Page, A. G.

2006-01-01

The application of lamp phosphors for accidental dosimetry is a new concept. Since the materials used in fluorescent lamps are good photo luminescent materials, if one can either use the inherent defects present in the phosphor or add suitable modifiers to induce thermoluminescence (TL) in these phosphors, then the device (fluorescent lamp) can be used as an accidental dosemeter. In continuation of our search for a suitable phosphor material, which can serve both as an efficient lamp phosphor and as a good radiation monitoring device, detailed examination has been carried out on cerium and terbium-doped lanthanum phosphate material. A 90 Sr beta source with 50 mCi strength (1.85 GBq) was used as the irradiation source for TL studies. The TL response as a function of dose received was examined for all phosphors used and it was observed that the intensity of the TL peak vs. dose received was a linear function in the dose range 0.1-200 Gy in each case. Incidentally LaPO 4 :Ce,Tb is a component of the compact fluorescent lamp marketed recently as an energy bright light source. Besides having very good luminescence efficiency, good dosimetric properties of these phosphors render them useful for their use in accidental dosimetry also. (authors)

A novel high color purity blue-emitting phosphor: CaBi{sub 2}B{sub 2}O{sub 7}:Tm{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Li, Jiangong, E-mail: lijiangong01@gmail.com [Department of Electronic Science and Engineering, Huanghuai University, Zhumadian 463000 (China); Yan, Huifang [Department of Foreign Languages and Literature, Huanghuai University, Zhumadian 463000 (China); Yan, Fengmei [Department of Chemistry and Chemical Engineering, Huanghuai University, Zhumadian 463000 (China)

2016-07-15

Graphical abstract: - Highlights: • A series of Tm{sup 3+}-doped CaBi{sub 2}B{sub 2}O{sub 7} blue-emitting phosphors were prepared. • The optimum doping content of Tm{sup 3+} ions was found. • The critical distance and concentration quenching mechanism was discussed. • The color purity of as prepared sample was analyzed and compared. - Abstract: A series of Tm{sup 3+}-doped CaBi{sub 2−x}B{sub 2}O{sub 7}:xTm{sup 3+} (0.02 ≤ x ≤ 0.12) blue-emitting phosphors with high color purity were prepared by solid-state reaction method. The crystal structure and luminescence properties of the as-prepared phosphors were studied. This phosphor shows a satisfactory blue performance (peak at 453 nm) due to the {sup 1}D{sub 2} → {sup 3}F{sub 4} transition of Tm{sup 3+} excited by 357 nm light. Investigation of Tm{sup 3+} content dependent emission spectra indicates that x = 0.04 is the optimum doping content of Tm{sup 3+} ions in the CaBi{sub 2}B{sub 2}O{sub 7} host. The critical distance and the concentration quenching mechanism were also investigated. In particular, the color purity of as prepared sample was analyzed and the result shows that the color purity of CaBi{sub 2}B{sub 2}O{sub 7}:Tm{sup 3+} is higher than the commercial blue phosphor BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} (BAM:Eu{sup 2+}) and the latest reported Tm{sup 3+} doped blue phosphors. The present work suggests that the CaBi{sub 2}B{sub 2}O{sub 7}:Tm{sup 3+} phosphor is a potential blue-emitting candidate for the application in the near-UV WLEDs.

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.

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.

Structural and luminescence effects of Ga co-doping on Ce-doped yttrium aluminate based phosphors

Energy Technology Data Exchange (ETDEWEB)

Ayvacikli, M. [Celal Bayar University, Faculty of Arts and Sciences, Department of Physics, Muradiye, Manisa (Turkey); Canimoglu, A. [Nigde University, Faculty of Arts and Sciences, Physics Department, Nigde (Turkey); Muresan, L.E., E-mail: laura_muresan2003@yahoo.com [Babes Bolyai University, Raluca Ripan Institute for Research in Chemistry, Fantanele 30, 400294 Cluj-Napoca (Romania); Barbu Tudoran, L. [Babes Bolyai University, Electronic Microscopy Centre, Clinicilor 37, 400006 Cluj Napoca (Romania); Garcia Guinea, J. [Museo Nacional Ciencias Naturales, Jose Gutierrez Abascal 2, Madrid 28006 (Spain); Karabulut, Y. [Celal Bayar University, Faculty of Arts and Sciences, Department of Physics, Muradiye, Manisa (Turkey); Jorge, A. [Museo Nacional Ciencias Naturales, Jose Gutierrez Abascal 2, Madrid 28006 (Spain); Karali, T. [Ege University, Institute of Nuclear Sciences, 35100 Bornova, İzmir (Turkey); Can, N., E-mail: cannurdogan@yahoo.com [Celal Bayar University, Faculty of Arts and Sciences, Department of Physics, Muradiye, Manisa (Turkey); Jazan University, Physics Department, P.O. Box 114, 45142 Jazan (Saudi Arabia)

2016-05-05

Herein, we primarily focus on luminescence spectrum measurements of various types of green emitting yttrium aluminate phosphors modified with gallium (Y{sub 3}Al{sub 5-x}Ga{sub x}O{sub 12}) synthesised by solid state reaction. The luminescent emission of samples depends on sample temperature and excitation radiation such as incident X-ray, electron and laser beam. Here, we measured radioluminescence (RL), cathodoluminescence (CL), photoluminescence (PL) along with XRD in order to clarify relationship between lattice defects and the spectral luminescence emissions. The RL and CL spectra of YAG:Ce exhibit an emission band ranging from 300 to 450 nm related to Y{sub Al} antisite defects. The broad emission band of garnet phosphors is shifted from 526 nm to 498 nm with increasing of Ga{sup 3+} content, while full width at half maximum (FWHM) of the band tends to be greater than the width of unmodified YAG:Ce garnet. Deconvolution of the spectrum reveals that three emission bands centred at 139, 234 and 294 °C occur in aluminate host garnets. - Highlights: • We present preparation of YAG:Ce{sup 3+}, Ga{sup 3+} phosphors by a solid state reaction method. • The shape and size of phosphor particles were investigated. • The luminescence properties were studied by different excitation sources.

Synthesis of Eu{sub x}Si{sub 6-z}Al{sub z}O{sub z}N{sub 8-z} green phosphor and its luminescent properties

Energy Technology Data Exchange (ETDEWEB)

Ryu, Jeong Ho; Won, Hyong Sik; Park, Youn-Gon; Kim, Sang Hyun; Song, Won Young; Suzuki, Hideo; Yoon, Chulsoo [Samsung Electro-Mechanics Co., LTD, Corporate R and D Institute, Suwon, Gyunggi-Do (Korea)

2009-06-15

Rare-earth-doped oxynitride or nitride compounds have been reported to be photoluminescent and may then serve as new phosphors because of their good thermal and chemical stabilities. In this work, Eu{sup 2+}-doped {beta}-SiAlON phosphor with a composition of Eu{sub x}Si{sub 6-z}Al{sub z}O{sub z}N{sub 8-z} (x=0.018,z=0.23) was prepared by gas-pressured solid state reaction. The crystallinity and particle morphology of the prepared phosphor were characterized. The Stokes shift and zero-phonon line were calculated mathematically and estimated from the spectral data. The temperature dependence of photoluminescence was measured from 25 to 250 C. The prepared Eu{sup 2+}-doped {beta}-SiAlON green phosphor showed superior thermal quenching property compared to silicate (SrBaSiO{sub 4}:Eu{sup 2+}) green phosphor. The white light-emitting diode (LED) back-lighting unit (BLU) using the prepared {beta}-SiAlON:Eu{sup 2+} green phosphor exhibited higher color gamut than a commercial silicate phosphor. (orig.)

Recent advances in rare earth doped alkali-alkaline earth borates for solid state lighting applications

Science.gov (United States)

Verma, Shefali; Verma, Kartikey; Kumar, Deepak; Chaudhary, Babulal; Som, Sudipta; Sharma, Vishal; Kumar, Vijay; Swart, Hendrik C.

2018-04-01

As a novel class of inorganic phosphor, the alkali-alkaline earth borate phosphors have gained huge attention due to their charming applications in solid-state lighting (SSL) and display devices. The current research drive shows that phosphors based on the alkali-alkaline earth borates have transformed the science and technology due to their high transparency over a broad spectral range, their flexibility in structure and durability for mechanical and high-laser applications. Recent advances in various aspects of rare-earth (RE) doped borate based phosphors and their utilizations in SSL and light emitting diodes are summarized in this review article. Moreover, the present status and upcoming scenario of RE-doped borate phosphors were reviewed in general along with the proper credential from the existing literature. It is believed that this review is a sole compilation of crucial information about the RE-doped borate phosphors in a single platform.

Laser discrimination by stimulated emission of a phosphor

Science.gov (United States)

Mathur, V. K.; Chakrabarti, K.

1991-01-01

A method for discriminating sources of UV, near infrared, and far infrared laser radiation was discovered. This technology is based on the use of a single magnesium sulfide phosphor doubly doped with rare earth ions, which is thermally/optically stimulated to generate colors correlatable to the incident laser radiation. The phosphor, after initial charging by visible light, exhibits green stimulated luminescence when exposed to a near infrared source (Nd: YAG laser). On exposure to far infrared sources (CO2 laser) the phosphor emission changes to orange color. A UV laser produces both an orange red as well as green color. A device using this phosphor is useful for detecting the laser and for discriminating between the near infrared, far infrared, and UV lasers. The technology is also capable of infrared laser diode beam profiling since the radiation source leaves an imprint on the phosphor that can be photographed. Continued development of the technology offers potential for discrimination between even smaller bandwidths within the infrared spectrum, a possible aid to communication or wavemixing devices that need to rapidly identify and process optical signals.

Photoluminescence analysis of Ce3+:Zn2SiO4 & Li++ Ce3+:Zn2SiO4: phosphors by a sol-gel method

Science.gov (United States)

Babu, B. Chandra; Vandana, C. Sai; Guravamma, J.; Rudramadevi, B. Hemalatha; Buddhudu, S.

2015-06-01

Here, we report on the development and photoluminescence analysis of Zn2SiO4, Ce3+:Zn2SiO4 & Li+ + Ce3+: Zn2SiO4 novel powder phosphors prepared by a sol-gel technique. The total amount of Ce3+ ions was kept constant in this experiment at 0.05 mol% total doping. The excitation and emission spectra of undoped (Zn2SiO4) and Ce3+ doped Zn2SiO4 and 0.05 mol% Li+ co-doped samples have been investigated. Cerium doped Zn2SiO4 powder phosphors had broad blue emission corresponding to the 2D3/2→2FJ transition at 443nm. Stable green-yellow-red emission has been observed from Zn2SiO4 host matrix and also we have been observed the enhanced luminescence of Li+ co-doped Zn2SiO4:Ce3+. Excitation and emission spectra of these blue luminescent phosphors have been analyzed in evaluating their potential as luminescent screen coating phosphors.

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.

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.

Induced assembly and photoluminescence of lanthanum (Tb, Eu, Dy) complexes/ZnO/polyethylene glycol hybrid phosphors

Energy Technology Data Exchange (ETDEWEB)

Yan Bing [Department of Chemistry, Tongji University, Siping Road 1239, Shanghai 200092 (China)]. E-mail: byan@tongji.edu.cn; Chen Xi [Department of Chemistry, Tongji University, Siping Road 1239, Shanghai 200092 (China); Wu Jianhua [Department of Chemistry, Tongji University, Siping Road 1239, Shanghai 200092 (China)

2007-08-31

Some novel kinds of hybrid phosphors were assembled with lanthanum (Tb, Eu, Dy) complexes (with four kinds of terbium complexes is 2,4-dihydroxybenzonic acid (DHBA), 1,10-phenanthroline (phen), acetylacetone (AA) and nicotinic acid (Nic), respectively) doped ZnO/PEG particles by co-precipitation approach derived from Zn(CH{sub 3}COO){sub 2} (Zn(AC){sub 2}), NaOH, PEG as precursors at room temperature. The characteristic luminescence spectra for f-f transitions of Tb{sup 3+}, Eu{sup 3+}, Dy{sup 3+} were observed. It is worthy to point out that ZnO is the excellent host for lanthanum ions by the assembly of PEG matrices.

Luminescence and energy transfer of Tm3+ or/and Dy3+ co-doped in Sr3Y(PO4)3 phosphors with UV excitation for WLEDs

International Nuclear Information System (INIS)

Wang, Jiyou; Wang, Jianbo; Duan, Ping

2014-01-01

Powder samples Sr 3 Y 1−x−y (PO 4 ) 3 :xTm 3+ -yDy 3+ were synthesized by the conventional solid-state reaction method. By appropriate tuning of activator content, the emission color can be adjusted around blue to white and yellow. It was discovered that the energy transfer from Tm 3+ to Dy 3+ was demonstrated to be via the intensity of Dy 3+ emission increase with the increase of Tm 3+ concentration. By changing the doping concentration of Tm 3+ and Dy 3+ in Sr 3 Y(PO 4 ) 3 , white-emitting phosphors are produced by 350 nm excitation wavelength, their corresponding color coordinates are very close to the white color chromaticity coordinates (x=0.33, y=0.33). Finally, Sr 3 Y 1−x−y (PO 4 ) 3 :xTm 3+ −yDy 3+ phosphors could be a good promising single-component white light-emitting UV-convertible phosphor in the field of white LEDs. -- Highlights: • The Sr 3 Y 1−x−y (PO 4 ) 3 :xTm 3+ −yDy 3+ phosphors were synthesized by the conventional solid-state reaction method. • The energy transfer in between Tm 3+ and Dy 3+ was observed and explained. • The phosphors can be efficiently excited by a UV light. • The Sr 3 Y 1−x−y (PO 4 ) 3 :xTm 3+ -yDy 3+ phosphor could be a better candidate white phosphor for UV W-LEDs

Fabrication and characterization of thin-film phosphor combinatorial libraries

Science.gov (United States)

Mordkovich, V. Z.; Jin, Zhengwu; Yamada, Y.; Fukumura, T.; Kawasaki, M.; Koinuma, H.

2002-05-01

The laser molecular beam epitaxy method was employed to fabricate thin-film combinatorial libraries of ZnO-based phosphors on different substrates. Fabrication of both pixel libraries, on the example of Fe-doped ZnO, and spread libraries, on the example of Eu-doped ZnO, has been demonstrated. Screening of the Fe-doped ZnO libraries led to the discovery of weak green cathodoluminescence with the maximum efficiency at the Fe content of 0.58 mol %. Screening of the Eu-doped ZnO libraries led to the discovery of unusual reddish-violet cathodoluminescence which is observed in a broad range of Eu concentration. No photoluminescence was registered in either system.

TL-OSL study of Li{sub 3}PO{sub 4}: Mg, Cu phosphor

Energy Technology Data Exchange (ETDEWEB)

Rahangdale, S. R., E-mail: sachin.rahangdale1@gmail.com; Wankhede, S. P. [Department of Physics, K.D.K.College of Engineering, Nagpur (India); Dhabekar, B. S. [RPAD, Bhabha Atomic Research Centre, Trombay, Mumbai 400085 (India); Palikundwar, U. A.; Moharil, S. V. [Department of Physics, RTM Nagpur University, Nagpur, 440010 (India)

2015-08-28

In the present work, we report the thermoluminescence and optically stimulated luminescence properties of Mg and Cu doped Li{sub 3}PO{sub 4} phosphor. The phosphor was synthesized by precipitation method. The thermoluminescence dosimetric peak temperature for the phosphor varies with concentrations of Mg and Cu. Li{sub 3}PO{sub 4} shows good response to 470nm optical stimulation. The OSL sensitivity of the phosphor is approximately 12 times than that of standard Lithium magnesium phosphate. This study may help to develop this material for the application in real time dosimetry using optically stimulated luminescence.

Investigation of Luminescence Characteristics of Some Synthetic Nano phosphors and Possibility of Application in Mixed Field Radiation Detection

International Nuclear Information System (INIS)

Ahmed, N.Y.A.

2013-01-01

The work given in this thesis aimed at Fabrication of high quality nano phosphor particles for getting high sensitive thermoluminescence material to use as ionizing radiation dosimeter. Ca Sr S nano phosphor has been prepared by solid state diffusion reaction method. The prepared nano phosphor was then activated with proper addition of some rare earth elements (dysprosium and gadolinium) for the sake of improving its TL sensitivity. The doped Ca Sr S nano phosphor was then treated by different courses of heat annealing for dual sake and regeneration. High temperature and high gamma dose sensitization are also used to increase sensitivity of Ca Sr S doped. By this means the TL-intensity of treated samples proved about 24 times observed enhancement. The prepared Ca Sr S: Dy nano phosphor is very reliable as pure gamma dosimeter for various applications such as personal, environmental and clinical dosimetry.

Frequency upconversion fluorescence studies of Er{sup 3+}/Yb{sup 3+}-codoped KNbO{sub 3} phosphors

Energy Technology Data Exchange (ETDEWEB)

Balakrishnaiah, R. [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Kim, Dong Woo [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Yi, Soung Soo, E-mail: ssyi@silla.ac.k [Department of Electronic Materials Engineering, Silla University, Busan 617-736 (Korea, Republic of); Kim, Kwang Duk; Kim, Sung Hoon [Department of Engineering in Energy and Applied Chemistry, Silla University, Busan 617-736 (Korea, Republic of); Jang, Kiwan; Lee, Ho Sueb [Department of Physics, Changwon National University, Changwon 641-773 (Korea, Republic of); Jeong, Jung Hyun [Department of Physics, Pukyong National University, Busan 608-737 (Korea, Republic of)

2009-05-29

Different concentrations of Er{sup 3+} and Yb{sup 3+} ions-doped potassium niobate (K{sub 0.9}NbO{sub 3}:Yb{sub (x)}Er{sub (0.1-x)} for x = 0, 0.01, 0.05, 0.09 and 0.1) polycrystalline powder phosphors were prepared by the conventional solid state reaction method and were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM) techniques. Energy transfer and upconversion fluorescence properties of the Yb{sup 3+} and Er{sup 3+}-codoped phosphors have been discussed. The XRD data has shown mono-phase for pure KNbO{sub 3} while the doped samples represented additional phase formation. The SEM micrographs represented the rectangular crystal growth habit for the KNbO{sub 3} phosphors when doped with 0.1 mol of Er{sup 3+} ions. An intense green emission at 557 nm along with a red emission at 674 nm was observed when the doped samples were excited with 975 nm IR radiation. The upconversion mechanism has been discussed based on the excited state absorption and energy transfer mechanisms.

Photoluminescence, reddish orange long persistent luminescence and photostimulated luminescence properties of praseodymium doped CdGeO3 phosphor

International Nuclear Information System (INIS)

Jin, Yahong; Hu, Yihua; Chen, Li; Fu, Yinrong; Mu, Zhongfei; Wang, Tao; Lin, Jun

2014-01-01

Highlights: • A novel phosphor CdGeO 3 :Pr 3+ was synthesized successfully. • The persistent luminescence properties of CdGeO 3 :Pr 3+ were studied. • The photostimulated luminescence properties of CdGeO 3 :Pr 3+ were investigated. • The persistent and photostimulated luminescence mechanisms were discussed in detail. - Abstract: Praseodymium doped CdGeO 3 phosphors were prepared successfully by a conventional high temperature solid-state reaction method. It showed reddish orange long persistent luminescence (LPL) after the short UV-irradiation. The reddish orange photostimulated luminescence (PSL) was also observed upon near infrared stimulation at 980 nm after per-exposure into UV light. The origin of LPL and PSL was identified with the emission from Pr 3+ ions with the aid of traps in host lattice. The optimal concentration of Pr 3+ ions for the brightest photoluminescence (PL) emission and the best LPL characteristic were experimentally to be about 3% and 0.5 mol%, respectively. The trapping and de-trapping processes of charge carriers between shallower and deep traps were illustrated. A model was proposed on the basis of experimental results to study the mechanisms of LPL and PSL

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.

A comparison study of rhodamine B photodegradation over nitrogen-doped lamellar niobic acid and titanic acid under visible-light irradiation.

Science.gov (United States)

Li, Xiukai; Kikugawa, Naoki; Ye, Jinhua

2009-01-01

A solid-state reaction method with urea as a nitrogen precursor was used to prepare nitrogen-doped lamellar niobic and titanic solid acids (i.e., HNb(3)O(8) and H(2)Ti(4)O(9)) with different acidities for visible-light photocatalysis. The photocatalytic activities of the nitrogen-doped solid acids were evaluated for rhodamine B (RhB) degradation and the results were compared with those obtained over the corresponding nitrogen-doped potassium salts. Techniques such as XRD, BET, SEM, X-ray photoelectron spectroscopy, and UV-visible diffuse reflectance spectroscopy were adopted to explore the nature of the materials as well as the characteristics of the doped nitrogen species. It was found that the intercalation of the urea precursor helped to stabilize the layered structures of both lamellar solid acids and enabled easier nitrogen doping. The effects of urea intercalation were more significant for the more acidic HNb(3)O(8) sample than for the less acidic H(2)Ti(4)O(9). Compared with the nitrogen-doped KNb(3)O(8) and K(2)Ti(4)O(9) samples, the nitrogen-doped HNb(3)O(8) and H(2)Ti(4)O(9) solid acids absorb more visible light and exhibit a superior activity for RhB photodegradation under visible-light irradiation. The nitrogen-doped HNb(3)O(8) sample performed the best among all the samples. The results of the current study suggest that the protonic acidity of the lamellar solid-acid sample is a key factor that influences nitrogen doping and the resultant visible-light photocatalysis.

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

Low-temperature synthesis of Zn{sub 2}SiO{sub 4}:Mn green photoluminescence phosphor

Energy Technology Data Exchange (ETDEWEB)

Sivakumar, V. [Saveetha Engineering College, Thandalam, Chennai 602105 (India); Lakshmanan, Arunachalam, E-mail: arunachalamlakshmanan@yahoo.com [Saveetha Engineering College, Thandalam, Chennai 602105 (India); Kalpana, S.; Sangeetha Rani, R.; Satheesh Kumar, R. [Saveetha Engineering College, Thandalam, Chennai 602105 (India); Jose, M.T. [Radiological Safety Division, Indira Gandhi Centre for Atomic Research, Kalpakkam 603102 (India)

2012-08-15

Zn{sub 2}SiO{sub 4}:Mn green phosphor having comparable photoluminescence (PL) efficiency with commercial phosphor has been synthesized at 1000 Degree-Sign C using solid state reactions involving ZnO, silicic acid and manganese acetate. The water of crystallization attached to SiO{sub 2} in silicic acid whose dissociation at 1000 Degree-Sign C seem to promote the sintering efficiency of Zn{sub 2}SiO{sub 4}:Mn. Incremental ZnO addition and re-firing at 1000 Degree-Sign C promote the diffusion rate of ZnO and SiO{sub 2}. The formation of a single crystalline phase of willemite structure in the samples was confirmed by powder XRD measurements. The phosphor exhibit an intense excitation band centered around 275 nm and a relatively weak excitation centered around 380 nm while the broad band green emission peaks at 524 nm. Other parameters studied include PL spectra, grain morphology, ZnO/SiO{sub 2} molar ratio, Mn concentration, co-dopant/flux and the effect of chemical forms of Mn dopant as well as silica on the PL efficiency. - Highlights: Black-Right-Pointing-Pointer Synthesis of Zn{sub 2}SiO{sub 4}:Mn by solid state sintering at a low temperature of 1000 Degree-Sign C in air. Black-Right-Pointing-Pointer Dissociation of water of crystallization in silicic acid promote sintering efficiency. Black-Right-Pointing-Pointer Photoluminescence efficiency comparable with that of the commercial phosphor. Black-Right-Pointing-Pointer Enhancement in luminescence with MgCO{sub 3} co-doping and refiring as well as ZnO addition. Black-Right-Pointing-Pointer XRD confirm single phase willemite structure (rhombohedral) of Zn{sub 2}SiO{sub 4}:Mn.

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....

Luminescence properties and energy transfer investigations of Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ phosphors

International Nuclear Information System (INIS)

Yang, Zaifa; Xu, Denghui; Sun, Jiayue; Du, Jiangnan; Gao, Xuedong

2016-01-01

Highlights: • A phosphor Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ for UV-based white LEDs was firstly synthesized successfully. • The phase structure and photoluminescence properties of samples were studied in detail. • The energy transfer process from Ce"3"+ to Tb"3"+ ions was illustrated in detail. • Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ phosphor has potential applications as an UV-convertible phosphor for white light emitting diodes. - Abstract: A series of Ce"3"+ or Tb"3"+ doped and Ce"3"+/Tb"3"+ co-doped Sr_3Lu(PO_4)_3 phosphors were prepared via the conventional high temperature solid-state reaction. The phase structure, photoluminescence and energy transfer properties of samples were studied in detail. The optimal proportion of Ce"3"+ single doping is 4 mol% with maximal fluorescence intensity. The Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ phosphor shows both a blue emission (428 nm) from Ce"3"+ and a yellowish-green emission (545 nm) from Tb"3"+ with considerable intensity under ultraviolet (UV) excitation (268 nm). The energy transfer from Ce"3"+ to Tb"3"+ ions takes place in the Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ phosphor on the basis of the analysis of the luminescence spectra. The energy transfer mechanism from Ce"3"+ to Tb"3"+ ions was proved to be dipole–dipole interaction. The energy transfer behaviors in Sr_3Lu(PO_4)_3:Ce"3"+, Tb"3"+ phosphor is also investigated by the lifetime measurement. The results show that this phosphor has potential applications for UV white-light LEDs.

Blue to bluish-green tunable phosphor Sr2LiSiO4F:Ce3+,Tb3+ and efficient energy transfer for near-ultraviolet light-emitting diodes

International Nuclear Information System (INIS)

Xie, Mubiao; Zeng, Lihua; Ye, TingLi; Yang, Xi; Zhu, Xianmei; Peng, Siyun; Lei, Lei

2014-01-01

Ce 3+ and Tb 3+ activated Sr 2 LiSiO 4 F phosphors were prepared by a solid state reaction technique at high temperature, and their ultraviolet (UV)-visible spectroscopic properties were investigated. Under ultraviolet light excitation, Ce 3+ -doped Sr 2 LiSiO 4 F phosphors emit blue light (420 nm), while Tb 3+ -doped phosphors show yellowish green emission. Efficient energy transfer from Ce 3+ to Tb 3+ ions in co-doped samples was confirmed in terms of corresponding excitation and emission spectra. The energy transfer mechanism between Ce 3+ and Tb 3+ was discussed and demonstrated to be dipole–dipole interaction in Sr 2 LiSiO 4 F:Ce 3+ ,Tb 3+ phosphors. Due to energy transfer from Ce 3+ to Tb 3+ , Ce 3+ and Tb 3+ co-doped Sr 2 LiSiO 4 F phosphors show intense absorption in near-UV region, and present tunable emission from blue to bluish green under 360 nm light excitation. The results indicate that these phosphors can be considered as candidates for white LEDs pumped by n-UV chips. (paper)

Fracto- mechanoluminescence and thermoluminescence properties of orange-red emitting Eu{sup 3+} doped Ca{sub 2}Al{sub 2}SiO{sub 7} phosphors

Energy Technology Data Exchange (ETDEWEB)

Tiwari, Geetanjali, E-mail: geetanjali.tiwari10@gmail.com [School of Studies in Physics and Astrophysics, Pt. Ravishankar Shukla University, Raipur, C.G., 492010 (India); Brahme, Nameeta, E-mail: namitabrahme@gmail.com [School of Studies in Physics and Astrophysics, Pt. Ravishankar Shukla University, Raipur, C.G., 492010 (India); Sharma, Ravi [Department of Physics, Govt. Arts and Commerce Girls College, Devendra Nagar, Raipur, C.G. (India); Bisen, D.P.; Sao, Sanjay K. [School of Studies in Physics and Astrophysics, Pt. Ravishankar Shukla University, Raipur, C.G., 492010 (India); Khare, Ayush [Department of Physics, National Institute of Technology, Raipur - 492 010 (India)

2017-03-15

The suitability of nano-structured Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} phosphors for thermoluminescence and mechanoluminescence dosimeter were investigated. Europium doped di-calcium di-aluminum silicate phosphor was synthesised by the combustion assisted method and annealed at 1100 °C for 4 h in reducing and oxidizing environments. The prepared Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} phosphor was characterized by X-ray diffractometer (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM) with energy dispersive x-ray spectroscopy (EDX), photoluminescence (PL) and decay characteristics. The phase structure of sintered phosphor has akermanite type which belongs to the tetragonal crystallography; this structure is a member of the melilite group and forms a layered compound. The chemical composition of the sintered Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} phosphor was confirmed by EDX spectra. Mechanoluminescence (ML) and thermoluminescence (TL) studies revealed that the ML and TL intensity increases with activator concentration. Optimum ML was observed for the sample having 2 mol% of Eu ions. The TL intensity of Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} was recorded for different exposure times of γ -irradiation and it was observed that TL intensity is maximum for γ dose of 1770 Gy. The PL spectra indicated that Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} could be excited effectively by near ultraviolet (NUV) light and exhibited bright orange-red emission with excellent colour stability. CIE colour coordinates of the prepared Ca{sub 2}Al{sub 2}SiO{sub 7}:Eu{sup 3+} phosphor was found suitable as orange-red light emitting phosphor with a CIE value of (x=0.6142, y=0.3849) and correlated colour temperature (CCT) is 1250 K. Therefore, it is considered to be a new promising orange-red emitting phosphor for white light emitting diode (LED) application.

High-pressure liquid chromatography of trace elements: Determination of terbium in terbium doped gadolinium oxide sulphide phosphors

International Nuclear Information System (INIS)

Mazzucotelli, A.; Dadone, A.; Frache, R.; Baffi, F.; Genoa Univ.

1982-01-01

A detailed study of isocratic and gradient elution separations of lanthanides has been carried out. Analyses of industrially and scientifically interesting products such as luminescent phosphors have been carried out by gradient elution with DL-2-hydroxyisobutyric acid. The determination of small amounts of terbium in gadolinium oxide sulphide phosphors is described in which an HCl solution was eluted through a stainless steel column packed with microparticulate silica, with bonded cation-exchange groups. Complete separation of gadolinium and terbium is achieved. Detection is with a variable wavelength detector following post-column complex formation with 4-(2-pyridylazo)-resorcinol monosodium salt. Results obtained on test solutions show good reproducilbity and sensitivtiy and the method may be considered sufficiently reliable to be used in routine quality control procedures. (orig.)

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

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....

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

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.

Energy transfer between Pr3+ and Mn2+ in K2YZr(PO4)3: Pr, Mn phosphor

International Nuclear Information System (INIS)

Liang Wei; Wang Yuhua

2011-01-01

Research highlights: → Pr 3+ , Mn 2+ co-doped K 2 YZr(PO 4 ) 3 phosphor is a novel type of practical visible quantum cutting phosphor in promising application. → The optimal quantum efficiency (QE) of this co-doped system K 2 YZr(PO 4 ) 3 : Pr 3+ , Mn 2+ reached to 126.3%. → The Mn 2+6 A 1g → 4 E g - 4 A 1g transition was found to coincide well with the 1 S 0 → 1 I 6 transition of Pr 3+ . → The energy transfer from Pr 3+ to Mn 2+ was also observed, converting the first photon from the PCE of Pr 3+ into the red emission of Mn 2+ , and the QC process occurred in this Pr 3+ , Mn 2+ co-doped K 2 YZr(PO 4 ) 3 phosphor. - Abstract: Pr 3+ , Mn 2+ co-doped K 2 YZr(PO 4 ) 3 samples were prepared by solid-state reaction method and their photoluminescence (PL) properties were investigated in ultra-violet (UV) and vacuum ultra-violet (VUV) region. The results indicated that in Pr 3+ singly doped K 2 YZr(PO 4 ) 3 sample, the first-step transition ( 1 S 0 → 1 I 6 , 3 P J around 405 nm) of Pr 3+ is near the ultraviolet (UV) range, not useful for practical application. When Mn 2+ was doped as a co-activator ion, the energy of 1 S 0 → 1 I 6 , 3 P J transition can be transferred synchronously from Pr 3+ to Mn 2+ and then emit a visible photon. The optimal quantum efficiency (QE) of this co-doped system K 2 YZr(PO 4 ) 3 : Pr 3+ , Mn 2+ reached to 126.3%, suggesting a novel type of practical visible quantum cutting phosphor in promising application.

Novel UV-emitting single crystalline film phosphors grown by LPE method

International Nuclear Information System (INIS)

Zorenko, Y.; Gorbenko, V.; Savchyn, V.; Voznyak, T.; Nikl, M.; Mares, J.A.; Winnacker, A.

2010-01-01

This work reports the development of new types of UV-emitting phosphors based on single crystalline films (SCF) of aluminum garnet and perovskite compounds grown by the liquid phase epitaxy method. We consider peculiarities of the growth and the luminescent and scintillation properties of the following four types of UV SCF phosphors: i) Ce-doped SCF of Y-Lu-Al-perovskites with the Ce 3+ emission in the 300-450 nm range of the decay time of 16-17 ns; ii) Pr-doped SCF of Y-Lu-Al garnets and perovskites with the Pr 3+ emission in the 300-400 nm and 235-330 nm ranges with the decay time of 13-19 and 7-8 ns, respectively; iii) La 3+ or Sc 3+ doped SCF of Y-Lu-Al-garnets, emitting in the 280-400 nm range due to formation of the La Y,Lu , Sc Y,Lu and Sc Al centers with decay time of the order of several hundreds of nanoseconds; iv) Bi 3+ doped SCF of garnets with Bi 3+ emission in 275-350 nm with decay time of about 1.9 μs.

Energy transfer and tunable multicolor emission and paramagnetic properties of GdF3:Dy(3+),Tb(3+),Eu(3+) phosphors.

Science.gov (United States)

Guan, Hongxia; Sheng, Ye; Xu, Chengyi; Dai, Yunzhi; Xie, Xiaoming; Zou, Haifeng

2016-07-20

A series of Dy(3+), Tb(3+), Eu(3+) singly or doubly or triply doped GdF3 phosphors were synthesized by a glutamic acid assisted one-step hydrothermal method. The samples were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM) and photoluminescence (PL) spectroscopy. The results show that the synthesized samples are all pure GdF3. The obtained samples have a peanut-like morphology with a diameter of about 270 nm and a length of about 600 nm. Under UV excitation, GdF3:Dy(3+), GdF3:Tb(3+) and GdF3:Eu(3+) samples exhibit strong blue, green and red emissions, respectively. By adjusting their relative doping concentrations in the GdF3 host, the different color hues of green and red light are obtained by co-doped Dy(3+), Tb(3+) and Tb(3+), Eu(3+) ions in the GdF3 host, respectively. Besides, there exist two energy transfer pairs in the GdF3 host: (1) Dy(3+) → Tb(3+) and (2) Tb(3+) → Eu(3+). More significantly, in the Dy(3+), Tb(3+), and Eu(3+) tri-doped GdF3 phosphors, white light can also be achieved upon excitation of UV light by adjusting the doping concentration of Eu(3+). In addition, the obtained samples also exhibit paramagnetic properties at room temperature (300 K) and low temperature (2 K). It is obvious that multifunctional Dy(3+), Tb(3+), Eu(3+) tri-doped GdF3 materials including tunable multicolors and intrinsic paramagnetic properties may have potential applications in the field of full-color displays.

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