Removal of some Fission Products from Low Level Liquid Radioactive Waste by Chemical Precipitation liquid/Co-precipitation / Phosphate Coagulant

International Nuclear Information System (INIS)

Borai, E.H.; Attallah, M.F.; Hilal, M.A.; Abo-Aly, M.M.; Shehata, F.A.

2008-01-01

In Egypt radioactive waste has been generated from various uses of radioactive materials. Presence of cesium demonstrated a major problem from the removal point of view even by conventional and advanced technologies. Selective chemical precipitation has been oriented for removal of some fission products including 137 Cs from low level liquid radioactive waste (LLLRW). The aim of the present study was focused to investigate the effectiveness of various phosphate compounds that improved the precipitation process and hence the decontamination factor. The results showed that, maximum removal of 137 Cs reaching 46.4 % using di-sodium hydrogen phosphate as a selective coagulant. It was found that significant enhancement of co-precipitation of 137 Cs (62.5 %) was obtained due to presence of Nd 3+ in the LLLRW

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

Synthesis and characterization of magnetite nanoparticles via the chemical co-precipitation method

International Nuclear Information System (INIS)

Petcharoen, K.; Sirivat, A.

2012-01-01

Highlights: ► Size-controlled magnetite nanoparticles were prepared via the chemical co-precipitation method in the range of 10–40 nm. ► The electrical conductivity of the smallest particle size is 1.3 × 10 −3 S/cm which belongs to the semiconductor material group. ► The surface modification of magnetite nanoparticles can provide the suspension stability over 1 week. - Abstract: Magnetite nanoparticles were synthesized via the chemical co-precipitation method using ammonium hydroxide as the precipitating agent. The size of the magnetite nanoparticles was carefully controlled by varying the reaction temperature and through the surface modification. Herein, the hexanoic acid and oleic acid were introduced as the coating agents during the initial crystallization phase of the magnetite. Their structure and morphology were characterized by the Fourier transform infrared spectroscopy (FTIR), the X-ray diffraction (XRD) and the field-emission scanning electron microscopy (FE-SEM). Moreover, the electrical and magnetic properties were studied by using a conductivity meter and a vibrating sample magnetometer (VSM), respectively. Both of the bare magnetite and the coated magnetite were of the cubic spinel structure and the spherical-shaped morphology. The reaction temperature and the surface modification critically affected the particle size, the electrical conductivity, and the magnetic properties of these particles. The particle size of the magnetite was increased through the surface modification and reaction temperature. In this study, the particle size of the magnetite nanoparticles was successfully controlled to be in the range of 10–40 nm, suitable for various biomedical applications. The electrical conductivity of the smallest particle size was 1.3 × 10 −3 S/cm, within the semi-conductive materials range, which was higher than that of the largest particle by about 5 times. All of the magnetite nanoparticles showed the superparamagnetic behavior with

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

Phosphorous adsorption and precipitation in a permeable reactive wall: Applications for wastewater disposal systems

International Nuclear Information System (INIS)

Baker, M.J.; Blowes, D.W.; Placek, C.J.

1997-01-01

A permeable reactive mixture has been developed using low cost, readily available materials that is capable of providing effective, long-term phosphorous treatment in areas impacted by on-land wastewater disposal. The reactive mixture creates a geochemical environment suitable for P-attenuation by both adsorption and precipitation reactions. Potential benefits include significant reductions in phosphorous loading to receiving groundwater and surface water systems, and the accumulation of P-mass in a finite and accessible volume of material. The mixture may be applied as a component within surface treatment systems or in subsurface applications such as horizontal or vertical permeable reactive walls. The mixture averaged > 90% treatment efficiency over 3.6 years of continuous-flow laboratory column experiments. The mixture was further evaluated at the pilot-scale to treat municipal wastewater, and the field-scale to treat a well-characterized septic system plume using an in situ funnel and gate system. Average PO 4 -P concentrations in effluent exiting the reactive mixture range between 0 - 0.3 mg/L. Mineralogical analyses have isolated the phases responsible for phosphorous uptake, and discrete phosphate precipitates have been identified

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.

Thermoluminescence of CaCO3:Dy and CaCO3:Mn

International Nuclear Information System (INIS)

Bapat, V.N.; Nambi, K.S.V.

1976-01-01

CaCO 3 samples doped with Dy and Mn were prepared in the laboratory by co-precipitation techniques. Thermoluminescence and emission spectra of these phosphors were studied and were compared with those of the naturally occuring calcite and undoped CaCO 3 samples. Dy-doping seems to give a more efficient phosphor and indicates a possibility of getting a better phosphor by a judicious choice of a rare earth doping of CaCO 3 . Interesting result have been obtained on the TL glow curve variations of these phosphors with different temperature treatments prior to irradiation. (author)

Wet milling versus co-precipitation in magnetite ferrofluid preparation

Directory of Open Access Journals (Sweden)

Almásy László

2015-01-01

Full Text Available Various uses of ferrofluids for technical applications continuously raise the interest in improvement and optimization of preparation methods. This paper deals with preparation of finely granulated magnetite particles coated with oleic acid in hydrocarbon suspensions following either chemical co-precipitation from iron salt precursors or wet milling of micron size magnetite powder with the goal to compare the benefits and disadvantages of each method. Microstructural measurements showed that both methods gave similar magnetite particle size of 10-15 nm. Higher saturation magnetization was achieved for the wet-milled magnetite suspension compared to relatively rapid co-precipitation synthesis. Different efficacies of ferrophase incorporation into kerosene could be related to the different mechanisms of oleic acid bonding to nanoparticle surface. The comparative data show that wet milling represents a practicable alternative to the traditional co-precipitation since despite of longer processing time, chemicals impact on environment can be avoided as well as the remnant water in the final product.

Assessing potential impacts of phosphate precipitation on nitrous oxide emissions and the carbon footprint of wastewater treatment plants.

Science.gov (United States)

Kosse, Pascal; Lübken, Manfred; Schmidt, Torsten C; Lange, Ruben-Laurids; Wichern, Marc

2018-02-15

Metal salts are widely used for the precipitation of phosphorus during wastewater treatment transforming soluble orthophosphate to an insoluble salt. In practice, more complex reactions are taking place including a reduction of the chemical solubility of dissolved greenhouse gases, such as nitrous oxide, present in the wastewater stream. In this respect, it was postulated that phosphorous precipitation will lead to artificial N 2 O stripping and hence to an increased carbon footprint of wastewater treatment plants. From lab-scale experiments utilizing N 2 O-saturated synthetic sewage solutions, it was evidenced that metal salt addition leads to N 2 O stripping with 20.8 g N 2 O per liter for a FeCl 2 -based precipitant to 26.4 g N 2 O per liter for a Al n (OH) m Cl3 n-m -based precipitant. Taking this maximum potential stripping effect into account for a carbon footprint analysis, a potential contribution of 16.11 kg CO 2,eq ·PE -1 ·a -1 was calculated in a case study, where FeCl 3 was considered. With respect to the defined system boundary conditions, the overall on-site and off-site CO 2 emissions were raised by 34% from 46.87 kg CO 2,eq ·PE -1 ·a -1 to 62.97 kg CO 2,eq ·PE -1 ·a -1 through CO 2,eq coming from phosphorous precipitation.

Chemical process for recovery of uranium values contained in phosphoric mineral lixivia

International Nuclear Information System (INIS)

Conceicao, E.L.H. da; Awwal, M.A.; Coelho, S. V.

1980-01-01

A recovery process of uranium values from phosporic mineral lixivia for obtaining uranio oxide concentrate adjusted to specifications of purity for its commercialization the process consists of the adjustment of electromotive force of lixiviem to suitable values for uranium extraction, extraction with organic solvent containing phosphoric acid ester and oxidant reextraction from this solvent with phosphoric acid solution, suggesting a new solvent extraction containing synergetic mixture of di-2-ethyl hexyl phosphoric acid and tri-octyl phosphine, leaching this solvent with water and re-extraction/precipitation with ammonium carbonate solution, resulting in the formation of uranyl tricarbonate and ammonium, that by drying and calcination gives the uranium oxide with purity degree for commercialization. (M.C.K.) [pt

Synthesis and luminescence properties of nanocrystalline LiF:Mg,Cu,P phosphor

Energy Technology Data Exchange (ETDEWEB)

Sahare, P.D., E-mail: pdsahare@physics.du.ac.i [Department of Physics and Astrophysics, University of Delhi, Delhi 110 007 (India); Bakare, J.S. [SSGM College of Engineering, Amravati University, Shegaon 444 203, Maharashtra (India); Dhole, S.D. [Department of Physics, University of Pune, Ganeshkhind, Pune 411 007 (India); Ingale, N.B. [Department of Physics, Professor Ram Meghe Institute of Technology and Research, Badnera-Amravati 444 605, Maharashtra (India); Rupasov, A.A. [P. N. Lebedev Physical Institute, Russian Academy of Sciences, Leninsky pr-t 53, Moscow (Russian Federation)

2010-02-15

Nanocrystalline LiF:Mg,Cu,P phosphor material of different shapes and sizes (microcrystalline cubic shape, nanorod shape and nanocrystalline cubical shaped) have been prepared by the chemical co-precipitation method. Thermoluminescence (TL) and other dosimetric characteristics of the phosphor are studied and presented here. The formation of the materials was confirmed by the X-ray diffraction (XRD). Its shapes and sizes were also observed using scanning electron microscope (SEM). The TL glow curve of the microcrystalline powder shows a prominent single peak at 408 K along with another peak of lesser intensity at around 638 K. On the contrary, the nanocrystalline rod shaped particles show a peak of low intensity at 401 K and a prominent peak around 700 K while the nanocrystalline particles in cubical shapes again show two peaks, one at around 407 K and the other at around 617 K, of which the lower temperature (407 K) peak is more prominent. The glow curve structure changes at very high doses (100 kRad) and some new peaks appear at around 525 and 637 K also the first peak appearing at around 401 K becomes prominent. The observed changes in TL due to the change in the shape and sizes of the nanophosphor have been reported. The PL has also been studied and various excitation and emission peaks observed due to the presence of various impurities are explained. The observed results have been explained in the light of asymmetrical crystal field effects due to asymmetrical shapes of the nanocrystalline phosphor. The comparison of these properties with the microcrystalline material prepared by the same co-precipitation method is also done.

Influence of phosphorous addition on Bi3Mo2Fe1 oxide catalysts for the oxidative dehydrogenation of 1-butene

KAUST Repository

Park, Jung-Hyun

2016-01-22

Bi3Mo2Fe1Px oxide catalysts were prepared by a co-precipitation method and the influence of phosphorous content on the catalytic performance in the oxidative dehydrogenation of 1-butene was investigated. The addition of phosphorous up to 0.4mole ratio to Bi3Mo2Fe1 oxide catalyst led to an increase in the catalytic performance; however, a higher phosphorous content (above P=0.4) led to a decrease of conversion. Of the tested catalysts, Bi3Mo2Fe1P0.4 oxide catalyst exhibited the highest catalytic performance. Characterization results showed that the catalytic performance was related to the quantity of a π-allylic intermediate, facile desorption behavior of adsorbed intermediates and ability for re-oxidation of catalysts. © 2015 Korean Institute of Chemical Engineers, Seoul, Korea

Influence of phosphorous addition on Bi3Mo2Fe1 oxide catalysts for the oxidative dehydrogenation of 1-butene

KAUST Repository

Park, Jung-Hyun; Shin, Chae-Ho

2016-01-01

Bi3Mo2Fe1Px oxide catalysts were prepared by a co-precipitation method and the influence of phosphorous content on the catalytic performance in the oxidative dehydrogenation of 1-butene was investigated. The addition of phosphorous up to 0.4mole ratio to Bi3Mo2Fe1 oxide catalyst led to an increase in the catalytic performance; however, a higher phosphorous content (above P=0.4) led to a decrease of conversion. Of the tested catalysts, Bi3Mo2Fe1P0.4 oxide catalyst exhibited the highest catalytic performance. Characterization results showed that the catalytic performance was related to the quantity of a π-allylic intermediate, facile desorption behavior of adsorbed intermediates and ability for re-oxidation of catalysts. © 2015 Korean Institute of Chemical Engineers, Seoul, Korea

Concentration-dependent luminescence and energy transfer of flower-like Y2(MoO4)3:Dy3+ phosphor

International Nuclear Information System (INIS)

Tian Yue; Chen Baojiu; Tian Bining; Hua Ruinian; Sun Jiashi; Cheng Lihong; Zhong Haiyang; Li Xiangping; Zhang Jinsu; Zheng Yanfeng; Yu Tingting; Huang Libo; Meng Qingyu

2011-01-01

Highlights: → Flower-shaped Y 2 (MoO 4 ) 3 phosphors were prepared by a co-precipitation method. → The structure and morphology of the prepared phosphors were characterized. → Energy transfer between Dy 3+ was studied by Huang's theory, IH and Uitert's models. - Abstract: Flower-like Y 2 (MoO 4 ) 3 :Dy 3+ phosphors have been synthesized via a co-precipitation approach with the aid of β-cyclodextrin. The crystal structure and morphology of the phosphors were characterized by XRD (X-ray diffraction) and FE-SEM (field emission scanning electron microscopy), respectively. The excitation and emission properties of the phosphors were examined by fluorescence spectroscopy. The dependence of color coordinates on the Dy 3+ doping concentration was analyzed. The energy transfer mechanism between Dy 3+ ions was studied based on the Huang's theory, I-H and Van Uitert's models. It was concluded simultaneously from these three routes that the electric dipole-dipole interaction between Dy 3+ ions is the main physical mechanism for the energy transfers between Dy 3+ .

PEG capped CaS nanoparticles synthesized by wet chemical co-precipitation method

Science.gov (United States)

Rekha, S.; Anila, E. I.

2018-04-01

Calcium sulfide (CaS) nanoparticles capped with polyethyleneglycol (PEG) were synthesized using wet chemical co-precipitation method. The structural and optical properties of the prepared sample were studied by X-ray diffractogram (XRD), transmission electron microscopy (TEM), diffuse reflectance spectrum (DRS) and photoluminescence (PL) spectrum. The structure of CaS nanoparticles is cubic as demonstrated by the X-ray powder diffraction (XRD) and selected area electron diffraction (SAED) analysis. TEMimage revealed the spherical morphology of the particles with diameter in the range 15-20 nm. The optical band gap of the prepared sample was determined from the DRS and its value was found to be 4.1 eV. The PL studies showed that the relative intensity of the PEG capped CaS nanoparticles was higher than that of uncapped CaS nanoparticles. The presence of various functional groups in the capped samples were examined by Fourier Transform Infrared (FTIR) spectroscopy.

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)

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

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.

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

High-efficient, bicolor-emitting GdVO_4:Dy"3"+ phosphor under near ultraviolet excitation

International Nuclear Information System (INIS)

Lu, Jinjin; Zhou, Jia; Jia, Huayu; Tian, Yue

2015-01-01

Bicolor emitting GdVO_4:Dy"3"+ phosphor with short columniation-shape was prepared via a simple co-precipitation process. The optimal doping concentration for obtaining maximal luminescent intensity was confirmed to be 0.3 mol% and the electric dipole–dipole interaction is responsible for concentration quenching of Dy"3"+ emission in GdVO_4 phosphor. In order to evaluate the luminescent performance of as-prepared phosphor, the luminescent efficiency and color coordinates were studied. The results show that luminescent efficiency of this phosphor is very high under near UV excitation and twice times higher than commercial Y_2O_2S:Eu"3"+ phosphor. In addition, the color coordinates for optimal Dy"3"+ concentration are (0.339, 0.379), which are close to equal energy point. Therefore, the GdVO_4:Dy"3"+ phosphor may have potential application for solid state lighting.

PRECIPITATION BEHAVIOR OF Co PHASES IN B2-ORDERED(Ni,Co)Al COMPOUND

Institute of Scientific and Technical Information of China (English)

W.H. Tian; A.L. Fan; M. Nemoto

2002-01-01

The precipitation behavior of Co phases in B2-ordered (Ni, Co)Al has been investigatedin terms of transmission electron microscopy. Fine precipitation off cc-Co occurs in(Ni, Co)Al by aging at temperature over 973K. The orientation relationship betweenthe fcc-Co precipitates and the B2-(Ni, Co)Al matrix follows the Kurdjumow-Sachs(K-S) orientation relation. But when the aging temperature is under 873K the Coprecipitates have a hcp crystal structure. The orientation relationship between thehcp-Co precipitates and the B2-(Ni, Co)Al matrix follows the Burgers orientation re-lation. (Ni, Co)Al is hardened appreciably by the fine precipitation of both the fcc-Coand hcp-Co phases. The temperature dependence of the yield strength of precipitate-containing B2-ordered (Ni, Co)Al was investigated by compression tests over the rangeof 298-1273K. The fine precipitation of Co phases enhances greatly the low and in-termediate temperature yield strength. When the deformation temperature was over873K, the strength of precipitate-containing (Ni, Co)Al is comparable to ternary dual-phase (Ni, Co)Al+Ni3Al alloy.

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.

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.

Study of calcium carbonate and sulfate co-precipitation

KAUST Repository

Zarga, Y.

2013-06-01

Co-precipitation of mineral based salts in scaling is still not well understood and/or thermodynamically well defined in the water industry. This study focuses on investigating calcium carbonate (CaCO3) and sulfate mixed precipitation in scaling which is commonly observed in industrial water treatment processes including seawater desalination either by thermal-based or membrane-based processes. Co-precipitation kinetics were studied carefully by monitoring several parameters simultaneously measured, including: pH, calcium and alkalinity concentrations as well as quartz microbalance responses. The CaCO3 germination in mixed precipitation was found to be different than that of simple precipitation. Indeed, the co-precipitation of CaCO3 germination time was not anymore related to supersaturation as in a simple homogenous precipitation, but was significantly reduced when the gypsum crystals appeared first. On the other hand, the calcium sulfate crystals appear to reduce the energetic barrier of CaCO3 nucleation and lead to its precipitation by activating heterogeneous germination. However, the presence of CaCO3 crystals does not seem to have any significant effect on gypsum precipitation. IR spectroscopy and the Scanning Electronic Microscopy (SEM) were used to identify the nature of scales structures. Gypsum was found to be the dominant precipitate while calcite and especially vaterite were found at lower proportions. These analyses showed also that gypsum crystals promote calcite crystallization to the detriment of other forms. © 2013 Elsevier Ltd.

Research of chemical structure of atmospheric precipitation

International Nuclear Information System (INIS)

Korenyak, D.

2001-01-01

The structure of atmospheric precipitation changes in its passing through the air medium. Thus, the atmospheric precipitation is one of the ecological factors, acting regularly. The research of chemical structure of atmospheric precipitation is closely connected with the problems of turnover of elements, with sanitary - ecological conditions of regions, with the matters of agricultural equipment and of salt balance of the soils. In paper the author for the first time represents the data on chemical structure of precipitation in the town. The data of chemical analysis of 18 samples are given. Obtained results permitted, to a certain extent, to determine the mechanisms of formation of atmospheric precipitation in the region investigated and its genesis. (authors)

Removal of ammonia from landfill leachate by struvite precipitation with the use of low-cost phosphate and magnesium sources.

Science.gov (United States)

Huang, Haiming; Xiao, Dean; Zhang, Qingrui; Ding, Li

2014-12-01

This paper presents a study concerning ammonia removal from landfill leachate by struvite precipitation with the use of waste phosphoric acid as the phosphate source. The results indicated that the Al(3+) ions present in the waste phosphoric acid significantly affected the struvite precipitation, and a removal ratio of ammonia close to that of pure phosphate salts could be achieved. Nevertheless, large amounts of NaOH were necessary to neutralize the H(+) present in the waste phosphoric acid. To overcome this problem, a low-cost magnesium source was proposed to be used as well as an alkali reagent in the struvite precipitation. The ammonia removal ratios were found to be 83%, with a remaining phosphate of 56 mg/L, by dosing the low-cost MgO in the Mg:N:P molar ratio of 3:1:1. An economic analysis showed that using waste phosphoric acid plus the low-cost MgO could save chemical costs by 68% compared with the use of pure chemicals. Post-treatment employment of a biological anaerobic filter process demonstrated that the high concentration of Mg(2+) remaining in the effluent of the struvite precipitation has no inhibitory effect on the performance of the biological treatment. Copyright © 2014 Elsevier Ltd. All rights reserved.

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.

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.)

The Synthesis of Calcium Salt from Brine Water by Partial Evaporation and Chemical Precipitation

Science.gov (United States)

Lalasari, L. H.; Widowati, M. K.; Natasha, N. C.; Sulistiyono, E.; Prasetyo, A. B.

2017-02-01

In this study would be investigated the effects of partial evaporation and chemical precipitation in the formation of calcium salt from brine water resources. The chemical reagents used in the study was oxalate acid (C2H2O4), ammonium carbonate (NH4)2CO3) and ammonium hydroxide (NH4OH) with reagent concentration of 2 N, respectively. The procedure was 10 liters brine water evaporated until 20% volume and continued with filtration process to separate brine water filtrate from residue (salt). Salt resulted from evaporation process was characterized by Scanning Electron Microscopy (SEM), X-Ray Fluorescence (XRF) and X-Ray Diffraction (XRD) techniques. Filtrate then was reacted with C2H2O4, (NH4)2CO3 and NH4OH reagents to get salt products in atmospheric condition and variation ratio volume brine water/chemicals (v/v) [10/1; 10/5; 10/10; 10/20; 10/30; 10:50; 20/1; 20/5; 20/10; 20/20; 20/30; 20:50]. The salt product than were filtered, dried, measured weights and finally characterized by SEM/EDS and XRD techniques. The result of experiment showed the chemical composition of brine water from Tirta Sanita, Bogor was 28.87% Na, 9.17% Mg, 2.94% Ca, 22.33% O, 0.71% Sr, 30.02% Cl, 1.51% Si, 1.23% K, 0.55% S, 1.31% Al. The chemical composition of salt resulted by partial evaporation was 53.02% Ca, 28.93%O, 9.50% Na, 2.10% Mg, 1.53% Sr, 1.20% Cl, 1.10% Si, 0.63% K, 0.40% S, 0.39% Al. The salt resulted by total evaporation was indicated namely as NaCl. Whereas salt resulted by partial evaporation was CaCO3 with a purity of 90 % from High Score Plus analysis. In the experiment by chemical precipitation was reported that the reagents of ammonium carbonate were more reactive for synthesizing calcium salt from brine water compared to reagents of oxalate acid and ammonium hydroxide. The salts precipitated by NH4OH, (NH4)2CO3, and H2C2O4 reagents were indicated as NaCl, CaCO3 and CaC2O4.H2O, respectively. The techniques of partial evaporation until 20% volume sample of brine water and

Formation of Silica-Lysozyme Composites Through Co-Precipitation and Adsorption

Directory of Open Access Journals (Sweden)

Daniela B. van den Heuvel

2018-04-01

Full Text Available Interactions between silica and proteins are crucial for the formation of biosilica and the production of novel functional hybrid materials for a range of industrial applications. The proteins control both precipitation pathway and the properties of the resulting silica–organic composites. Here, we present data on the formation of silica–lysozyme composites through two different synthesis approaches (co-precipitation vs. adsorption and show that the chemical and structural properties of these composites, when analyzed using a combination of synchrotron-based scattering (total scattering and small-angle X-ray scattering, spectroscopic, electron microscopy, and potentiometric methods vary dramatically. We document that while lysozyme was not incorporated into nor did its presence alter the molecular structure of silica, it strongly enhanced the aggregation of silica particles due to electrostatic and potentially hydrophobic interactions, leading to the formation of composites with characteristics differing from pure silica. The differences increased with increasing lysozyme content for both synthesis approaches. Yet, the absolute changes differ substantially between the two sets of composites, as lysozyme did not just affect aggregation during co-precipitation but also particle growth and likely polymerization during co-precipitation. Our results improve the fundamental understanding of how organic macromolecules interact with dissolved and nanoparticulate silica and how these interactions control the formation pathway of silica–organic composites from sodium silicate solutions, a widely available and cheap starting material.

Formation of Silica-Lysozyme Composites Through Co-Precipitation and Adsorption

Science.gov (United States)

van den Heuvel, Daniela B.; Stawski, Tomasz M.; Tobler, Dominique J.; Wirth, Richard; Peacock, Caroline L.; Benning, Liane G.

2018-04-01

Interactions between silica and proteins are crucial for the formation of biosilica and the production of novel functional hybrid materials for a range of industrial applications. The proteins control both precipitation pathway and the properties of the resulting silica-organic composites. Here we present data on the formation of silica-lysozyme composites through two different synthesis approaches (co-precipitation vs. adsorption) and show that the chemical and structural properties of these composites, when analyzed using a combination of synchrotron-based scattering (total scattering and SAXS), spectroscopic, electron microscopy and potentiometric methods vary dramatically. We document that while lysozyme was not incorporated into nor did its presence alter the molecular structure of silica, it strongly enhanced the aggregation of silica particles due to electrostatic and potentially hydrophobic interactions, leading to the formation of composites with characteristics differing from pure silica. The differences increased with increasing lysozyme content for both synthesis approaches. Yet, the absolute changes differ substantially between the two sets of composites, as lysozyme did not just affect aggregation during co-precipitation but also particle growth and likely polymerization during co-precipitation. Our results improve the fundamental understanding of how organic macromolecules interact with dissolved and nanoparticulate silica and how these interactions control the formation pathway of silica-organic composites from sodium silicate solutions, a widely available and cheap starting material.

Heavy metal immobilization via microbially induced carbonate precipitation and co-precipitation

Science.gov (United States)

Lauchnor, E. G.; Stoick, E.

2017-12-01

Microbially induced CaCO3 precipitation (MICP) has been successfully used in applications such as porous media consolidation and sealing of leakage pathways in the subsurface, and it has the potential to be used for remediation of metal and radionuclide contaminants in surface and groundwater. In this work, MICP is investigated for removal of dissolved heavy metals from contaminated mine discharge water via co-precipitation in CaCO3 or formation of other metal carbonates. The bacterially catalyzed hydrolysis of urea produces inorganic carbon and ammonium and increases pH and the saturation index of carbonate minerals to promote precipitation of CaCO3. Other heavy metal cations can be co-precipitated in CaCO3 as impurities or by replacing Ca2+ in the crystal lattice. We performed laboratory batch experiments of MICP in alkaline mine drainage sampled from an abandoned mine site in Montana and containing a mixture of heavy metals at near neutral pH. Both a model bacterium, Sporosarcina pasteurii, and a ureolytic bacterium isolated from sediments on the mine site were used to promote MICP. Removal of dissolved metals from the aqueous phase was determined via inductively coupled plasma mass spectrometry and resulting precipitates were analyzed via electron microscopy and energy dispersive x-ray spectroscopy (EDX). Both S. pasteurii and the native ureolytic isolate demonstrated ureolysis, increased the pH and promoted precipitation of CaCO3 in batch tests. MICP by the native bacterium reduced concentrations of the heavy metals zinc, copper, cadmium, nickel and manganese in the water. S. pasteurii was also able to promote MICP, but with less removal of dissolved metals. Analysis of precipitates revealed calcium carbonate and phosphate minerals were likely present. The native isolate is undergoing identification via 16S DNA sequencing. Ongoing work will evaluate biofilm formation and MICP by the isolate in continuous flow, gravel-filled laboratory columns. This research

Tailoring particle size and morphology of colloidal Ag particles via chemical precipitation for Ag-BSCCO composites

International Nuclear Information System (INIS)

Medendorp, N.W. Jr.; Bowman, K.J.; Trumble, K.P.

1996-01-01

The chemical precipitation of silver particles is an effective method for tailoring the particle size and morphology. This article investigates a chemical precipitation method for producing silver colloids, and how processing parameters affected particle size, morphology and adherence. Decreasing the silver nitrate concentration during precipitation with sodium borohydride decreased the colloidal silver particle size. Decreasing the addition rate of the reducing agent produced faceted particles. Reversing the reactant addition order also changed the particle size and the morphology. Precipitated colloids demonstrated a difference between the growth-dominated and the equilibrium structures. Co-dispersing Bi-based superconducting platelets during precipitation allowed Ag colloids to preferentially nucleate on the platelets and to remain adhered even after the additional processing. (orig.)

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.

Preparation of palladium nanoparticles on alumina surface by chemical co-precipitation method and catalytic applications

Energy Technology Data Exchange (ETDEWEB)

Kumar, Avvaru Praveen; Kumar, B. Prem; Kumar, A.B.V. Kiran; Huy, Bui The [Department of Chemistry, Changwon National University, Changwon 641-773 (Korea, Republic of); Lee, Yong-Ill, E-mail: yilee@changwon.ac.kr [Department of Chemistry, Changwon National University, Changwon 641-773 (Korea, Republic of)

2013-01-15

Highlights: Black-Right-Pointing-Pointer Facile synthesis of palladium nanoparticles on alumina surface. Black-Right-Pointing-Pointer The surface morphology and properties of the nanocrystalline powders were characterized. Black-Right-Pointing-Pointer The catalytic activities of palladium nanoparticles were investigated. - Abstract: The present work reports a chemical co-precipitation process to synthesize palladium (Pd) nanoparticles using alumina as a supporting material. The optimized temperature for the formation of nanocrystalline palladium was found to be 600 Degree-Sign C. The X-ray diffraction (XRD) and Raman spectroscopy were used to study the chemical nature of the Pd in alumina matrix. The surface morphology and properties of the nanocrystalline powders were examined using thermogravimetric analysis (TG-DTA), XRD, Raman spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM) and atomic force microscopy (AFM). The calcinations in different atmospheres including in the inert medium forms the pure nano Pd{sup 0} while in the atmospheric air indicates the existence pure Pd{sup 0} along with PdO nanoparticles. The catalytic activities of the as-synthesized nanocrystalline Pd nanoparticles in the alumina matrix were investigated in Suzuki coupling, Hiyama cross-coupling, alkene and alkyne hydrogenation, and aerobic oxidation reactions.

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.

Supercritical antisolvent co-precipitation of rifampicin and ethyl cellulose.

Science.gov (United States)

Djerafi, Rania; Swanepoel, Andri; Crampon, Christelle; Kalombo, Lonji; Labuschagne, Philip; Badens, Elisabeth; Masmoudi, Yasmine

2017-05-01

Rifampicin-loaded submicron-sized particles were prepared through supercritical anti-solvent process using ethyl cellulose as polymeric encapsulating excipient. Ethyl acetate and a mixture of ethyl acetate/dimethyl sulfoxide (70/30 and 85/15) were used as solvents for both drug and polymeric excipient. When ethyl acetate was used, rifampicin was crystallized separately without being embedded within the ethyl cellulose matrix while by using the ethyl acetate/dimethyl sulfoxide mixture, reduced crystallinity of the active ingredient was observed and a simultaneous precipitation of ethyl cellulose and drug was achieved. The effect of solvent/CO 2 molar ratio and polymer/drug mass ratio on the co-precipitates morphology and drug loading was investigated. Using the solvent mixture, co-precipitates with particle sizes ranging between 190 and 230nm were obtained with drug loading and drug precipitation yield from respectively 8.5 to 38.5 and 42.4 to 77.2% when decreasing the ethyl cellulose/rifampicin ratio. Results show that the solvent nature and the initial drug concentrations affect morphology and drug precipitation yield of the formulations. In vitro dissolution studies revealed that the release profile of rifampicin was sustained when co-precipitation was carried out with the solvent mixture. It was demonstrated that the drug to polymer ratio influenced amorphous content of the SAS co-precipitates. Differential scanning calorimetry thermograms and infrared spectra revealed that there is neither interaction between rifampicin and the polymer nor degradation of rifampicin during co-precipitation. In addition, stability stress tests on SAS co-precipitates were carried out at 75% relative humidity and room temperature in order to evaluate their physical stability. SAS co-precipitates were X-ray amorphous and remained stable after 6months of storage. The SAS co-precipitation process using a mixture of ethyl acetate/dimethyl sulfoxide demonstrates that this strategy can

Synthesis of Eu3+-doped calcium and strontium carbonate phosphors at room temperature

International Nuclear Information System (INIS)

Pan Yuexiao; Wu Mingmei; Su Qiang

2003-01-01

Red phosphors CaCO 3 :Eu 3+ and SrCO 3 :Eu 3+ have been prepared by co-precipitation with ammonium bicarbonate (NH 4 HCO 3 ) at room temperature. Pure calcite CaCO 3 can be obtained by prolonging the reaction time at 220 deg. C and it decomposes to cubic CaO at 1000 deg. C. Trivalent Eu 3+ acts as a luminescent probe to determine both the calcite and the mixed phase of calcite and vaterite phase of CaCO 3 host and to analyze its decomposition process. High temperature sintering improved both the crystallization and luminescence of SrCO 3 :Eu 3+ in aragonite phase

Vacuum ultraviolet excited photoluminescence properties of Gd2O2CO3:Eu3+ phosphor

Institute of Scientific and Technical Information of China (English)

WANG Zhilong; WANG Yuhua; ZHANG Jiachi

2008-01-01

The Gd2O2CO3:Eu3+ with type-II structure phosphor was successfully synthesized via flux method at 400℃ and their photoluminescence properties in vacuum ultraviolet (VUV) region were examined. The broad and strong excitation bands in the range of 153-205 nm owing to the CO32- host absorption and charge transfer (CT) of Gd3+-O2- were observed for Gd2O2CO3:Eu3+. Under 172 nm excitation, Gd2O2CO3:Eu3+ exhibited strong red emission with good color purity, indicating Eu3+ ions located at low symmetry sites and the chromaticity coordination of luminescence for Gd2O2CO3:Eu3+ was (x=0.652, y=0.345). The photoluminescence quenching concentration of Eu3+ excited by 172 nm for Gd2O2CO3:Eu3+ was about 5%. Gd2O2CO3:Eu3+ would be a potential VUV-excited red phosphor applied in mercury-free fluorescent lamps.

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.

CO2 (carbon dioxide) fixation by applying new chemical absorption-precipitation methods

International Nuclear Information System (INIS)

Park, Sangwon; Lee, Min-Gu; Park, Jinwon

2013-01-01

CO 2 (carbon dioxide) is the most common greenhouse gas and most of it is emitted from human activities. The methods for CO 2 emission reduction can be divided into physical, chemical, and biochemical methods. Among the physical and chemical methods, CCS (carbon capture and storage) is a well-known reducing technology. However, this method has many disadvantages including the required storage area. In general, CCS requires capture and storage processes. In this study, we propose a method for reusing the absorbed CO 2 either in nature or in industry. The emitted CO 2 was converted into CO 3 2− using a conversion solution, and then made into a carbonate by combining the conversion solution with metal ions at normal temperature and pressure. The resulting carbonate was analyzed using FT-IR (Fourier transform infrared spectroscopy) and XRD (X-ray diffraction). We verified the formation of a solid consisting of calcite and vaterite. In addition, the conversion solution that was used could be reused in the same process of CCS technology. Our study demonstrates a successful method of reducing and reusing emitted CO 2 , thereby making CO 2 a potential future resource. - Highlights: • This study focused on a new CO 2 fixation process method. • In CCS technology, the desorption process requires high thermal energy consumption. • This new method does not require a desorption process because the CO 2 is accomplished through CaCO 3 crystallization. • A new absorption method is possible instead of the conventional absorption-desorption process. • This is not only a rapid reaction for fixing CO 2 , but also economically feasible

Study of calcium carbonate and sulfate co-precipitation

KAUST Repository

Zarga, Y.; Ben Boubaker, H.; Ghaffour, NorEddine; Elfil, Hamza

2013-01-01

of CaCO3 nucleation and lead to its precipitation by activating heterogeneous germination. However, the presence of CaCO3 crystals does not seem to have any significant effect on gypsum precipitation. IR spectroscopy and the Scanning Electronic

Electrodialytic recovery of phosphorus from chemically precipitated sewage sludge ashes

DEFF Research Database (Denmark)

Parés Viader, Raimon; Jensen, Pernille Erland; Ottosen, Lisbeth M.

Phosphorus scarcity requires improved recover and reuse of urban sources; the recycling of this nutrient from sewage sludge has become increasingly important in the last years. Using an innovative electrodialytic process, the present study shows the potential for P separation from Fe and Al...... precipitated sewage sludge ash using this technique, with a recovery rate of around 70%. Furthermore, heavy metals were removed from the phosphorous fraction, producing a pure and safe phosphorus source in the end....

Electrodialytic recovery of phosphorus from chemically precipitated sewage sludge ashes

DEFF Research Database (Denmark)

Viader, Raimon Parés; Erland Jensen, Pernille; Ottosen, Lisbeth M.

Phosphorus scarcity requires improved recover and reuse of urban sources; the recycling of this nutrient from sewage sludge has become increasingly important in the last years. Using an innovative electrodialytic process, the present study shows the potential for P separation from Fe and Al...... precipitated sewage sludge ash using this technique, with a recovery rate of around 70%. Furthermore, heavy metals were removed from the phosphorous fraction, producing a pure and safe phosphorus source in the end...

Strontium isotope fractionation during strontianite (SrCO3) dissolution, precipitation and at equilibrium

Science.gov (United States)

Mavromatis, Vasileios; Harrison, Anna L.; Eisenhauer, Anton; Dietzel, Martin

2017-12-01

In this study we examine the behavior of stable Sr isotopes between strontianite [SrCO3] and reactive fluid during mineral dissolution, precipitation, and at chemical equilibrium. Experiments were performed in batch reactors at 25 °C in 0.01 M NaCl solutions wherein the pH was adjusted by bubbling of a water saturated gas phase of pure CO2 or atmospheric air. The equilibrium Sr isotope fractionation between strontianite and fluid after dissolution of the solid under 1 atm CO2 atmosphere was estimated as Δ88/86SrSrCO3-fluid = δ88/86Sr SrCO3 - δ88/86Srfluid = -0.05 ± 0.01‰. On the other hand, during strontianite precipitation, an enrichment of the fluid phase in 88Sr, the heavy isotopomer, was observed. The evolution of the δ88/86Srfluid during strontianite precipitation can be modeled using a Rayleigh distillation approach and the estimated, kinetically driven, fractionation factor αSrCO3-fluid between solid and fluid is calculated to be 0.99985 ± 0.00003 corresponding to Δ88/86SrSrCO3-fluid = -0.15‰. The obtained results further support that under chemical equilibrium conditions between solid and fluid a continuous exchange of isotopes occurs until the system approaches isotopic equilibrium. This isotopic exchange is not limited to the outer surface layer of the strontianite crystal, but extends to ∼7-8 unit cells below the crystal surface. The behavior of Sr isotopes in this study is in excellent agreement with the concept of dynamic equilibrium and it suggests that the time needed for achievement of chemical equilibrium is generally shorter compared to that for isotopic equilibrium. Thus it is suggested that in natural Sr-bearing carbonates an isotopic change may still occur close to thermodynamic equilibrium, despite no observable change in aqueous elemental concentrations. As such, a secondary and ongoing change of Sr isotope signals in carbonate minerals caused by isotopic re-equilibration with fluids has to be considered in order to use Sr

Study of structural and optical properties of ZnAlQ5 (zinc aluminum quinolate) organic phosphor for OLED applications

Science.gov (United States)

Nagpure, I. M.; Painuly, Deepshikha; Rabanal, Maria Eugenia

2016-05-01

The various composition of ZnAlQ5 such as Zn1.5A10.5Q5, Zn1Al1Q5, Zn0.5Al1.5Q5 organic phosphors were prepared via simple cost effective co-precipitation method. The FTIR, SEM, photoluminescence analysis of the prepared phosphors were reported. ZnQ2 and AlQ3 were also prepared by similar method and their properties were compared with different composition of ZnAlQ5. The structural elucidation in the form of stretching frequencies of chemical bonds of the prepared phosphor was carried out using Fourier Transform Infrared Spectroscopy (FTIR). The stretching frequency analysis confirms the formation of prepared phosphor materials. The SEM analysis shows the surface morphological behavior of prepared phosphor materials. Greenish photoluminescence were observed at 505 to 510 nm for the different composition of ZnAlQ5,in which Zn1.5Al0.5Q5 shows maximum luminescence intensity at 505 nm. PL emission of ZnQ2 was observed at 515 nm, while for AlQ3 at 520 nm. The blue shift of 10 nm was observed in Zn1.5A10.5Q5 due to modification of energy level due to presence of Zn2+ and Al3+. The enhancement in PL intensity was observed in Zn1.5A10.5Q5 compared to the other composition due to transfer of energy between Zn2+ and quinolate complex. Optical properties of the prepared materials were evaluated for possible applications in organic light emitting devices (OLED).

Facile solution-precipitation assisted synthesis and luminescence property of greenish-yellow emitting Ca{sub 6}Ba(PO{sub 4}){sub 4}O:Eu{sup 2+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Ji, Haipeng [School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, China University of Geosciences, Beijing 100083 (China); Huang, Zhaohui, E-mail: huang118@cugb.edu.cn [School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, China University of Geosciences, Beijing 100083 (China); Xia, Zhiguo, E-mail: xiazg@ustb.edu.cn [The Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology Beijing, Beijing 100083 (China); Xie, Yao [School of Materials Science and Technology, Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, China University of Geosciences, Beijing 100083 (China); Molokeev, Maxim S. [Laboratory of Crystal Physics, Kirensky Institute of Physics, SB RAS, Krasnoyarsk 660036 (Russian Federation); Department of Physics, Far Eastern State Transport University, Khabarovsk 680021 (Russian Federation); Atuchin, Victor V. [Laboratory of Optical Materials and Structures, Institute of Semiconductor Physics, SB RAS, Novosibirsk 630090 (Russian Federation); Functional Electronics Laboratory, Tomsk State University, Tomsk 634050 (Russian Federation); Laboratory of Semiconductor and Dielectric Materials, Novosibirsk State University, Novosibirsk 630090 (Russian Federation)

2016-03-15

Highlights: • Ca{sub 6}Ba(PO{sub 4}){sub 4}O:Eu{sup 2+} phosphor was prepared by the solution-precipitation assisted route. • The phosphors have satisfactory smooth grain surface and particle size. • It shows greenish-yellow color emission (maximum at 540 nm) upon blue light excitation. • Eu{sup 2+} is coordinated with isolated oxygen atoms and those from PO{sub 4} polyhedra. - Abstract: Greenish-yellow emitting microcrystalline Ca{sub 6}Ba(PO{sub 4}){sub 4}O:Eu{sup 2+} phosphor was successfully prepared by a solution-precipitation assisted high temperature reaction method. Phase structure, morphology and/or luminescence properties of the precursor and the as-prepared phosphors were characterized. The phase-pure Ca{sub 6}Ba(PO{sub 4}){sub 4}O:Eu{sup 2+} phosphors were obtained with smooth grain surface and particle size of 2–8 μm. Ca{sub 6}Ba(PO{sub 4}){sub 4}O:Eu{sup 2+} exhibits bright greenish-yellow color emission with its maximum at 540 nm upon UV-blue light excitation. The maximum position of the broad emission band is independent on the calcination temperature. The emission intensity increases with increasing calcination temperature due to improved crystallinity. Besides, the presence of two Eu{sup 2+} emission centers in the Ca{sub 6}Ba(PO{sub 4}){sub 4}O crystal lattice was confirmed and the coordination effects are considered concerning the roles of isolated O atoms and those from the PO{sub 4} tetrahedra.

Acoustic Monitoring of Gravity-Driven Controls on CaCO3 Precipitates in a Fracture

Science.gov (United States)

Xu, Z.; Sheets, J.; Zhang, L.; Kim, D.; Kneafsey, T. J.; Cole, D. R.; Jun, Y. S.; Pyrak-Nolte, L. J.

2017-12-01

Sealing fractures by mineral precipitation is an important process for improving caprock integrity in subsurface reservoirs. In this study, the ability to monitor precipitate distribution in fractures with buoyant fluids was examined. Fractures with uniform aperture distributions of 0.5, 1.0 and 2.0 mm were created from acrylic plates to enable direct imaging of precipitate formation over time. CaCO3 precipitation was induced in a fracture from invasion of 1M CaCl2 and 0.3M Na2CO3 solutions. During chemical invasion, a fracture plane was oriented either parallel or perpendicular to gravity. Acoustic (P) wave transmission ( 1 MHz) and optical imaging were used to monitor the sample prior to, during and after fluid injection. Complementary X-ray computed tomography was performed throughout the experiments on vertical fractures and post injection for the horizontal fractures. Precipitate particle sizes during formation were determined using SAXS and WAXS. In both horizontal and vertical fractures, the density contrast between the two solutions affected the spatial distribution of precipitation. In vertical fractures, the denser CaCl2 solution almost completely displaced the NaCO3 solution, causing strong localization of precipitates. However, in the horizontal fractures, flow stratification occurred in the 2 mm aperture fractures, with the less dense Na2CO3 flowing over the CaCl2 solution, resulting in a more even distribution of precipitates cross the fracture plane. P-wave amplitudes increased up to 8% and the arrival time decreased with precipitate accumulation in the horizontal fracture. This is consistent with a three-layered approach as the seismic impedance inside the fracture increases. The initial contact between the two was observed as a decrease in the P-wave amplitude. As precipitates accumulated, the amplitude recovered and increased, with greater increases observed along the mixing flow path. Fractures in the subsurface may seal differently depending on

Integrated chemical process for exothermic wave synthesis of high luminance YAG:Ce phosphors

International Nuclear Information System (INIS)

Won, C.W.; Nersisyan, H.H.; Won, H.I.; Youn, J.W.

2011-01-01

In this paper, high-luminance yellow-emitting Y 3 Al 5 O 12 :Ce 3+ phosphor (YAG:Ce) microparticles were prepared in a solid flame using a 1.425Y 2 O 3 +2.5Al 2 O 3 +0.15CeO 2 +k(KClO 3 +urea)+mNH 4 F precursor mixture (here k is the number of moles of the KClO 3 +urea red-ox mixture, and m is the number of moles of NH 4 F). The self-sustaining combustion process for the entire reaction sample was provided by the heat generated from the KClO 3 +urea mixture. Parametric studies demonstrated that the maximum temperature in the combustion wave varied from 885 to 1200 deg. C for k=2.0-3.0 mole and m=0-1.5 mole. X-ray analysis results showed that the product obtained in the solid flame consisted of Y 3 Al 5 O 12 :Ce 3+ and KCl phases. Therefore, after dissolving potassium chloride in distillated water, pure-phase YAG:Ce phosphor powder was obtained. The as-prepared YAG:Ce phosphor particles had diameters of 10-25 μm and good dispersity and exhibited luminescence properties comparable to those of YAG:Ce phosphor powders prepared by conventional high-temperature processing. - Highlights: → A new solid-flame strategy was developed for synthesizing high-luminance YAG:Ce phosphor. → Adding KClO 3 +CO(NH 2 ) 2 +NH 4 F mixture to oxide powders provides a low-temperature combustion process. → YAG:Ce phosphor particles 10-25 μm in diameter were obtained at 1000-1100 deg. C within tens of seconds. → As-prepared YAG:Ce emission intensity was 90.1-103.2% compared to that of the reference sample.

The development of new phosphors of Tb3+/Eu3+ co-doped Gd3Al5O12 with tunable emission

Science.gov (United States)

Teng, Xin; Wang, Wenzhi; Cao, Zhentao; Li, Jinkai; Duan, Guangbin; Liu, Zongming

2017-07-01

The gadolinium aluminum garnets Gd3Al5O12 (GdAG) activated with Tb3+/Eu3+ were successfully prepared via co-precipitation method at 1500 °C in this work. The crystal structure stabilization, elements analysis, microphotograph, PL/PLE spectra, decay behavior and quantum efficiency were discussed in detail. The metastable GdAG compounds been effectively stabilized by doping with smaller 10 at.% Tb3+, which then allows the development of new phosphors of (Gd0.9-xTb0.1Eux)3Al5O12 (GdAG:Tb3+/Eu3+, x = 0-0.03) for opto-functionality explorations. The PLE/PL spectra displays that the strongest PLE peak was located at ∼276 nm, which overlaps the 8S7/2 → 6IJ transition of Gd3+. Under 276 nm excitation, the phosphors exhibited both Tb3+ and Eu3+ emissions at 548 nm (green, 5D4 → 7F5 transition of Tb3+) and 592 nm (orange-red, 5D0 → 7F1 transition of Eu3+), respectively. The emission intensities of Tb3+ and Eu3+ remarkably varied with the Eu3+ incorporation. As a consequence, the emission color can be readily tuned from approximately green to orange-red. Fluorescence decay analysis found that the lifetime for the Tb3+ emission rapidly decreased conforming to the Tb3+ → Eu3+ energy transfer, and the energy transfer efficiency was calculated. Owing to the Gd3+ → Eu3+ and Gd3+ → Tb3+ energy transfer, the emission intensities of Tb3+ and Eu3+ in (Gd0.9-xTb0.1Eux)AG phosphor were higher than (Y0.87Tb0.1Eu0.03)AG and (Lu0.87Tb0.1Eu0.03)AG system. The (Gd0.9-xTb0.1Eux)AG garnet phosphors developed in this work may serve as a new type of phosphor which hopefully meets the requirements of various lighting and optical display applications.

Structure dependent luminescence characterization of green-yellow emitting Sr{sub 2}SiO{sub 4}:Eu{sup 2+} phosphors for near UV LEDs

Energy Technology Data Exchange (ETDEWEB)

Han, J.K. [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States); Hannah, M.E.; Piquette, A. [Central Research, OSRAM SYLVANIA, 71 Cherry Hill Drive Beverly, MA 01915 (United States); Hirata, G.A. [Centro de Nanociencias y Nanotecnolgia, Universidad Nacional Autonoma de Mexico, Km. 107 Carretera Tijuana-Ensenada Apdo, Ensenada, MX CP 22860 (Mexico); Talbot, J.B. [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States); Mishra, K.C. [Central Research, OSRAM SYLVANIA, 71 Cherry Hill Drive Beverly, MA 01915 (United States); McKittrick, J., E-mail: jmckittrick@ucsd.edu [University of California, San Diego, Materials Science and Engineering Program, La Jolla, CA 92093 (United States)

2012-01-15

This paper reports on the luminescence properties of mixtures of {alpha}- and {beta}-(Sr{sub 0.97}Eu{sub 0.03}){sub 2}SiO{sub 4} phosphors. These phosphors were prepared by 3 different synthesis techniques: a modified sol-gel/Pechini method, a co-precipitation method and a combustion method. The structural and optical properties of these phosphors were compared to those of solid state synthesized powders. The emission spectra consist of a weak broad blue band centered near 460 nm and a strong broad green-yellow band centered between 543 and 573 nm depending on the crystal structure. The green-yellow emission peak blue-shifts as the amount of {beta} phase increases and the photoluminescence emission intensity and quantum efficiency of the mixed phase powders is greater than those of predominant {alpha}-phase powders when excited between 370 and 410 nm. Thus, (Sr{sub 1-x}Eu{sub x}){sub 2}SiO{sub 4} with larger proportion of the {beta} phase are more promising candidates than single {alpha}-phase powders for use as a green-yellow emitting phosphor for near UV LED applications. Finally the phosphors prepared by the sol-gel/Pechini method, which have larger amount of {beta} phase, have a higher emission intensity and quantum efficiency than those prepared by co-precipitation or combustion synthesis. - Highlights: > Mixtures of {alpha}- and {beta}-Sr{sub 2}SiO{sub 4}:Eu{sup 2+} phosphors were prepared by 3 different synthesis methods. > Emission peak blue-shifts as the amount of {beta} phase increases. > Emission intensity and QE of the {alpha}+{beta} powders are greater than those of single {alpha} phase. > Phosphors prepared by sol-gel/Pechini have the highest emission intensity and QE.

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.

Effects of natural organic matter on calcium and phosphorus co-precipitation.

Science.gov (United States)

Sindelar, Hugo R; Brown, Mark T; Boyer, Treavor H

2015-11-01

Phosphorus (P), calcium (Ca) and natural organic matter (NOM) naturally occur in all aquatic ecosystems. However, excessive P loads can cause eutrophic or hyper-eutrophic conditions in these waters. As a result, P regulation is important for these impaired aquatic systems, and Ca-P co-precipitation is a vital mechanism of natural P removal in many alkaline systems, such as the Florida Everglades. The interaction of P, Ca, and NOM is also an important factor in lime softening and corrosion control, both critical processes of drinking water treatment. Determining the role of NOM in Ca-P co-precipitation is important for identifying mechanisms that may limit P removal in both natural and engineered systems. The main goal of this research is to assess the role of NOM in inhibiting Ca and P co-precipitation by: (1) measuring how Ca, NOM, and P concentrations affect NOM's potential inhibition of co-precipitation; (2) determining the effect of pH; and (3) evaluating the precipitated solids. Results showed that Ca-P co-precipitation occurs at pH 9.5 in the presence of high natural organic matter (NOM) (≈30 mg L(-1)). The supersaturation of calcite overcomes the inhibitory effect of NOM seen at lower pH values. Higher initial P concentrations lead to both higher P precipitation rates and densities of P on the calcite surface. The maximum surface density of co-precipitated P on the precipitated calcite surface increases with increasing NOM levels, suggesting that NOM does prevent the co-precipitation of Ca and P. Copyright © 2015 Elsevier Ltd. All rights reserved.

Luminescence properties of Ce3+ and Tb3+ co-activated ZnAl2O4 phosphor

International Nuclear Information System (INIS)

Tshabalala, K.G.; Cho, S.-H.; Park, J.-K.; Pitale, Shreyas S.; Nagpure, I.M.; Kroon, R.E.; Swart, H.C.; Ntwaeaborwa, O.M.

2012-01-01

In this study, a solution combustion method was used to prepare green emitting Ce 3+ –Tb 3+ co-activated ZnAl 2 O 4 phosphor. The samples were annealed at 700 °C in air or hydrogen atmosphere to improve their crystallinity and optical properties. X-ray diffraction study confirmed that both as-prepared and post-preparation annealed samples crystallized in the well known cubic spinel structure of ZnAl 2 O 4 . An agglomeration of irregular platelet-like particles whose surfaces were encrusted with smaller spheroidal particles was confirmed by scanning electron microscopy (SEM). The fluorescence data collected from the annealed samples with different concentrations of Ce 3+ and Tb 3+ show the enhanced green emission at 543 nm associated with 5 D 4 → 7 F 5 transitions of Tb 3+ . The enhancement was attributed to energy transfer from Ce 3+ to Tb 3+ . Possible mechanism of energy transfer via a down conversion process is discussed. Furthermore, cathodoluminescence (CL) intensity degradation of this phosphor was also investigated and the degradation data suggest that the material was chemically stable and the CL intensity was also stable after 10 h of irradiation by a beam of high energy electrons.

Photoluminescence properties and energy transfer of color tunable MgZn₂(PO₄)₂:Ce³⁺,Tb³⁺ phosphors.

Science.gov (United States)

Xu, Mengjiao; Wang, Luxiang; Jia, Dianzeng; Zhao, Hongyang

2015-11-21

A series of Ce(3+)/Tb(3+) co-doped MgZn2(PO4)2 phosphors have been synthesized by the co-precipitation method. Their structure, morphology, photoluminescence properties, decay lifetime, thermal stability and luminous efficiency were investigated. The possible energy transfer mechanism was proposed based on the experimental results and detailed luminescence spectra and decay curves of the phosphors. The critical distance between Ce(3+) and Tb(3+) ions was calculated by both the concentration quenching method and the spectral overlap method. The energy transfer mechanism from the Ce(3+) to Tb(3+) ion was determined to be dipole-quadrupole interaction, and the energy transfer efficiency was 85%. By utilizing the principle of energy transfer and appropriate tuning of Ce(3+)/Tb(3+) contents, the emission color of the obtained phosphors can be tuned from blue to green light. The MgZn2(PO4)2:Ce(3+),Tb(3+) phosphor is proved to be a promising UV-convertible material capable of green light emitting in UV-LEDs due to its excellent thermal stability and luminescence properties.

Recovery of valuable metals from waste cathode materials of spent lithium-ion batteries using mild phosphoric acid

Energy Technology Data Exchange (ETDEWEB)

Chen, Xiangping, E-mail: chenxiangping101@163.com [School of Environmental Science and Engineering, Shaanxi University of Science & Technology, Xi’an 710021 (China); College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China); Ma, Hongrui, E-mail: mahr@sust.edu.cn [School of Environmental Science and Engineering, Shaanxi University of Science & Technology, Xi’an 710021 (China); Luo, Chuanbao; Zhou, Tao [College of Chemistry and Chemical Engineering, Central South University, Changsha 410083 (China)

2017-03-15

Graphical abstract: Cobalt can be directly recovered as Co{sub 3}(PO{sub 4}){sub 2} from waste LiCoO{sub 2} using H{sub 3}PO{sub 4} as leaching and precipitating agent. - Highlights: • Phosphoric acid was innovatively used as leaching and precipitating agent. • Over 99% Co and Li can be separated and recovered in a single leaching step. • Co and Li can be separated under mild conditions of 40 °C and 0.7 M H{sub 3}PO{sub 4}. • Activation energy values for Co and Li are 7.3 and 10.168 kJ/mol. • Cobalt phosphate (97.1% in purity) can be obtained as the leaching product. - Abstract: Sustainable recycling of valuable metals from spent lithium-ion batteries (LIBs) may be necessary to alleviate the depletion of strategic metal resources and potential risk of environmental pollution. Herein a hydrometallurgical process was proposed to explore the possibility for the recovery of valuable metals from the cathode materials (LiCoO{sub 2}) of spent LIBs using phosphoric acid as both leaching and precipitating agent under mild leaching conditions. According to the leaching results, over 99% Co can be separated and recovered as Co{sub 3}(PO{sub 4}){sub 2} in a short-cut process involved merely with leaching and filtrating, under the optimized leaching conditions of 40 °C (T), 60 min (t), 4 vol.% H{sub 2}O{sub 2}, 20 mL g{sup −1} (L/S) and 0.7 mol/L H{sub 3}PO{sub 4}. Then leaching kinetics was investigated based on the logarithmic rate kinetics model and the obtained results indicate that the leaching of Co and Li fits well with this model and the activation energies (Ea) for Co and Li are 7.3 and 10.2 kJ/mol, respectively. Finally, it can be discovered from characterization results that the obtained product is 97.1% pure cobalt phosphate (Co{sub 3}(PO{sub 4}){sub 2}).

77 FR 66149 - Significant New Use Rules on Certain Chemical Substances

Science.gov (United States)

2012-11-02

... 835.5045 or OECD Test Guideline 302A); a UV/visible absorption test (OPPTS Test Guideline 830.7050... precipitate used to produce phosphors. Based on test data on analogous chemical substances, EPA identified...

Fluorescence properties of novel near-infrared phosphor CaSc{sub 2}O{sub 4}:Ce{sup 3+}, Nd{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Meng, J.X., E-mail: tmjx@jnu.edu.c [Department of Chemistry, Jinan University, Guangzhou 510632 (China); Institute of Nanochemistry, Jinan University, Guangzhou 510632 (China); Zhang, F.J.; Peng, W.F.; Wan, W.J.; Xiao, Q.L.; Chen, Q.Q.; Cao, L.W. [Department of Chemistry, Jinan University, Guangzhou 510632 (China); Wang, Z.L. [School of Chemistry and Biotechnology, Yunnan Nationalities University, Kunming 650031 (China)

2010-10-15

Research highlights: Novel near-infrared (NIR) phosphor, CaSc{sub 2}O{sub 4}:Ce{sup 3+}, Nd{sup 3+}, was synthesized. The phosphor gives strong Nd{sup 3+} characteristic NIR emissions in the range of 880-930 nm. The NIR emission intensity gets a 200 times enhancement benefited from the efficient energy transfer from a co-doped Ce{sup 3+}. The energy transfer mechanism was also briefly based on detailed investigation on spectrum and fluorescence lifetime. - Abstract: Novel near-infrared (NIR) phosphor, CaSc{sub 2}O{sub 4}:Ce{sup 3+}, Nd{sup 3+}, was synthesized by co-precipitation method followed by firing at 1300 {sup o}C in reduced atmosphere. When irradiated with blue light, the phosphor gives strong Nd{sup 3+} characteristic NIR emissions in the range of 880-930 nm. The NIR emission intensity gets a 200 times enhancement by co-doping of Ce{sup 3+}. Detailed investigation on spectrum and fluorescence lifetimes indicated the NIR luminescence enhancement is obtained from an energy transfer process. The process initiates with efficient absorption of blue light by Ce{sup 3+} ions via an allowed 4f-5d transition, follow by efficient energy transfer from Ce{sup 3+} to Nd{sup 3+}, and emitting strong Nd{sup 3+} characteristic fluorescence.

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.)

Synthesis, characterization and anti-bacterial activities of pure and Co-doped BaSO4 nanoparticles via chemical precipitation route.

Science.gov (United States)

Sivakumar, S; Soundhirarajan, P; Venkatesan, A; Khatiwada, Chandra Prasad

2015-02-25

In the present study, we reported that the synthesis and characterization of pure and diverse mole Co-doped BaSO4 nanoparticles have been synthesized by chemical precipitation technique. X-ray diffraction analysis (XRD) brought out the information about the synthesized products is orthorhombic structure and highly crystalline in nature. The average grain size of the samples was determined by using the Debye-Scherer's equation. The existence of functional groups and band area of the samples were confirmed by Fourier transform infrared (FTIR) spectroscopy. The direct and indirect band gap energy of pure and doped samples was carried out using UV-VIS-DRS. The surface micrograph, morphological distribution and elemental compositions of the synthesized products were assessed by scanning electron microscopy (SEM) and Energy dispersive X-ray (EDS). Thermo gravimetric and differential thermal analysis (TG-DTA) techniques were analyzed thermal behaviour of pure and Co-doped samples. Finally, antibacterial activities found the Gram-positive and Gram-negative bacteria are more active in transporter, dehydrogenize and periplasmic enzymatic activities of pure and doped samples. Copyright © 2014 Elsevier B.V. All rights reserved.

Synthesis and characterization of novel Na15 (SO4 )5 F4 Cl:Ce3+ halosulfate phosphors.

Science.gov (United States)

Bhake, A M; Nair, Govind B; Zade, G D; Dhoble, S J

2016-12-01

A series of Na 15 (SO 4 ) 5 F 4 Cl phosphors doped with Ce 3+ ions was prepared using the wet chemical method. X-Ray diffraction studies were used to determine their phase formation and purity. Fourier transform infrared spectroscopy effectively identified the chemical bonds present in the molecule. The photoluminescence properties of the as-prepared phosphors were investigated and the Ce 3+ ions in these hosts were found to give broadband emission in the UV range. For the thermoluminescence study, phosphors were irradiated with a 5 Gy dose of γ-rays from a 60 Co source. Chen's half-width method was employed to calculate the trapping parameters from the thermoluminescence glow curve. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

Microbial electrolysis desalination and chemical-production cell for CO2 sequestration

KAUST Repository

Zhu, Xiuping

2014-05-01

Mineral carbonation can be used for CO2 sequestration, but the reaction rate is slow. In order to accelerate mineral carbonation, acid generated in a microbial electrolysis desalination and chemical-production cell (MEDCC) was examined to dissolve natural minerals rich in magnesium/calcium silicates (serpentine), and the alkali generated by the same process was used to absorb CO2 and precipitate magnesium/calcium carbonates. The concentrations of Mg2+ and Ca2+ dissolved from serpentine increased 20 and 145 times by using the acid solution. Under optimal conditions, 24mg of CO2 was absorbed into the alkaline solution and 13mg of CO2 was precipitated as magnesium/calcium carbonates over a fed-batch cycle (24h). Additionally, the MEDCC removed 94% of the COD (initially 822mg/L) and achieved 22% desalination (initially 35g/L NaCl). These results demonstrate the viability of this process for effective CO2 sequestration using renewable organic matter and natural minerals. © 2014 Elsevier Ltd.

Synthesis and characterization of novel red emitting nanocrystal Gd6WO12:Eu3+ phosphors

International Nuclear Information System (INIS)

Tian Yue; Chen Baojiu; Hua Ruinian; Zhong Haiyang; Cheng Lihong; Sun Jiashi; Lu Weili; Wan Jing

2009-01-01

Novel nanosized Gd 6 WO 12 :Eu 3+ phosphors were synthesized via a co-precipitation reaction. The crystal structure and morphology of the phosphors were characterized by using X-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM). It was found that the resultant powders show a regular and sphere-like shape with average particle size of 60 nm. Intrinsic red emission originating from Eu 3+ was observed while excited at the W 6+ →O 2- and Eu 3+ →O 2- charge transfer bands or f-f absorption bands. The color coordinates of the phosphors were calculated to be x=0.625, y=0.375. The concentration dependence of the luminescence was studied, and optimum doping concentration for obtaining maximum emitting intensity was confirmed to be around 12 mol%. It was also found that the electric dipole-dipole interaction plays an important role for quenching luminescence of Eu 3+ .

Synthesis of Sr- and Mg- doped lanthanum gallate by carbonate co-precipitation

International Nuclear Information System (INIS)

Sunitha, Y.; Narasimham, K.V.N.S.V.P.L.; Raju, V.S.; Kumar, Sanjiv

2010-01-01

Sr- and Mg- doped lanthanum gallate (LSGM) are promising electrolytes for low temperature solid oxide fuel cells (SOFCs) in view of their high ionic conductivity and stability over a wide range of oxygen partial pressures. LSGM powders are usually prepared by solid-state reactions. However high sintering temperature (∼ 1500 deg C) required for densification and the formation of secondary phases are the major drawbacks of the method. Wet-chemical method is a suitable alternative to solid-state synthesis with the prospect of the realisation of phase pure material with good sinterability at comparatively lower temperatures. In this paper we present the results of our investigation on the synthesis of LaGaO 3 and LSGM by a wet-chemical method through carbonate co-precipitation using ammonium carbonate and ammonium bicarbonate as precipitants. Phase and microstructural evolution of the material have been studied by XRD and SEM respectively, while compositional analysis has been performed by ion beam analysis (IBA) techniques. In addition we have also investigated the incorporation of Sr and Mg in the lattice of LaGaO 3 by (a) solid-state reaction route and (b) wet-chemical approach

Evaluation of precipitates used in strainer head loss testing. Part I. Chemically generated precipitates

International Nuclear Information System (INIS)

Bahn, Chi Bum; Kasza, Ken E.; Shack, William J.; Natesan, Ken; Klein, Paul

2009-01-01

The purpose of the current program was to evaluate the properties of chemical precipitates proposed by industry that have been used in sump strainer head loss testing. Specific precipitates that were evaluated included aluminum oxyhydroxide (AlOOH) and sodium aluminum silicate (SAS) prepared according to the procedures in WCAP-16530-NP, along with precipitates formed from injecting chemicals into the test loop according to the procedure used by one sump strainer test vendor for U.S. pressurized water reactors. The settling rates of the surrogate precipitates are strongly dependent on their particle size and are reasonably consistent with those expected from Stokes' Law or colloid aggregation models. Head loss tests showed that AlOOH and SAS surrogates are quite effective in increasing the head loss across a perforated pump inlet strainer that has an accumulated fibrous debris bed. The characteristics of aluminum hydroxide precipitate using sodium aluminate were dependent on whether it was formed in high-purity or ordinary tap water and whether excess silicate was present or not.

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

Red Emission of SrAl2O4:Mn4+ Phosphor for Warm White Light-Emitting Diodes

Science.gov (United States)

Chi, N. T. K.; Tuan, N. T.; Lien, N. T. K.; Nguyen, D. H.

2018-05-01

In this work, SrAl2O4:Mn4+ phosphor is prepared by co-precipitation. The phase structure, morphology, composition and luminescent performance of the phosphor are investigated in detail with x-ray diffraction, field emission scanning electron microscopy, steady-state photoluminescence (PL) spectra, and temperature-dependent PL measurements. The phosphor shows a strong red emission peak at ˜ 690 nm, which is due to the transition between electronic levels and the electric dipole transition 2Eg to 4A2g of Mn4+ ions located at the sites with D3d local symmetry. The sample doped with 0.04 mol.% Mn4+ exhibits intense red emission with high thermal stability and appropriate International Commission on Illumination (CIE) coordinates (x = 0.6959, y = 0.2737). It is also found that the phosphor absorption in an extended band from 250 nm to 500 nm has three peaks at 320 nm, 405 nm, and 470 nm, which match well with the emission band of ultraviolet (UV) lighting emission diode (LED) or blue LED chips. These results demonstrate that SrAl2O4:Mn4+ phosphor can play the role of activator in narrow red-emitting phosphor, which is potentially useful in UV (˜ 320 nm) or blue (˜ 460 nm) LED.

Continuous tunable broadband emission of fluorphosphate glasses for single-component multi-chromatic phosphors.

Science.gov (United States)

Zheng, Ruilin; Zhang, Qi; Yu, Kehan; Liu, Chunxiao; Ding, Jianyong; Lv, Peng; Wei, Wei

2017-10-15

A kind of Sn 2+ /Mn 2+ co-doped fluorphosphate (FP) glasses that served as single-component continuous tunable broadband emitting multi-chromatic phosphors are developed for the first time. Importantly, these FP glasses have high thermal conductivity (3.25-3.70  W/m·K) and good chemical stability in water (80°C). By combining with commercially available UV-LEDs directly, the emission colors can be tuned from blue/cold-white to warm-white/red through the energy transfer from Sn 2+ to Mn 2+ , and the broadband spectra covering the whole visible region from 380 nm to 760 nm. Notably, the FP glass can also serve as a white light phosphor by controlling the content of SnO/MnO, which has excellent optical properties. The CIE chromaticity coordinate, color rendering index, and quantum efficiency are (0.33, 0.29), 84, and 0.952, respectively. These new phosphors, possessing good optical and chemical properties, are promising for applications in solid-state lighting devices.

Development of a calcium phosphate co-precipitate/poly(lactide-co-glycolide) DNA delivery system: release kinetics and cellular transfection studies.

Science.gov (United States)

Kofron, Michelle D; Laurencin, Cato T

2004-06-01

One of the most common non-viral methods for the introduction of foreign deoxyribonucleic acid (DNA) into cultured cells is calcium phosphate co-precipitate transfection. This technique involves the encapsulation of DNA within a calcium phosphate co-precipitate, particulate addition to in vitro cell culture, endocytosis of the co-precipitate, and exogenous DNA expression by the transfected cell. In this study, we fabricated a novel non-viral gene transfer system by adsorbing DNA, encapsulated in calcium phosphate (DNA/Ca-P) co-precipitates, to biodegradable two- and three-dimensional poly(lactide-co-glycolide) matrices (2D-DNA/Ca-P/PLAGA, 3D-DNA/Ca-P/PLAGA). Co-precipitate release studies demonstrated an initial burst release over the first 48 h. By day 7, approximately 96% of the initially adsorbed DNA/Ca-P co-precipitate had been released. This was followed by low levels of co-precipitate release for 42 days. Polymerase chain reaction was used to demonstrate the ability of the released DNA containing co-precipitates to transfect SaOS-2 cells cultured in vitro on the 3D-DNA/Ca-P/PLAGA matrix and maintenance of the structural integrity of the exogenous DNA. In summary, a promising system for the incorporation and controlled delivery of exogenous genes encapsulated within a calcium phosphate co-precipitate from biodegradable polymeric matrices has been developed and may have applicability to the delivery of therapeutic genes and the transfection of other cell types.

Study of structural and optical properties of ZnAlQ{sub 5} (zinc aluminum quinolate) organic phosphor for OLED applications

Energy Technology Data Exchange (ETDEWEB)

Nagpure, I. M., E-mail: indrajitnagpure@gmail.com; Painuly, Deepshikha [Physics, Department of Sciences and Humanities, National Institute of Technology,Uttarakhand-246174 (India); Rabanal, Maria Eugenia [Department of Materials Science and Engineering and Chemical Engineering,University Carlos III of Madrid, Avd. Universidad 30, 28911 Leganes, Madrid (Spain)

2016-05-06

The various composition of ZnAlQ{sub 5} such as Zn{sub 1.5}A{sub 10.5}Q{sub 5}, Zn{sub 1}Al{sub 1}Q{sub 5}, Zn{sub 0.5}Al{sub 1.5}Q{sub 5} organic phosphors were prepared via simple cost effective co-precipitation method. The FTIR, SEM, photoluminescence analysis of the prepared phosphors were reported. ZnQ{sub 2} and AlQ{sub 3} were also prepared by similar method and their properties were compared with different composition of ZnAlQ{sub 5}. The structural elucidation in the form of stretching frequencies of chemical bonds of the prepared phosphor was carried out using Fourier Transform Infrared Spectroscopy (FTIR). The stretching frequency analysis confirms the formation of prepared phosphor materials. The SEM analysis shows the surface morphological behavior of prepared phosphor materials. Greenish photoluminescence were observed at 505 to 510 nm for the different composition of ZnAlQ{sub 5},in which Zn{sub 1.5}Al{sub 0.5}Q{sub 5} shows maximum luminescence intensity at 505 nm. PL emission of ZnQ{sub 2} was observed at 515 nm, while for AlQ{sub 3} at 520 nm. The blue shift of 10 nm was observed in Zn{sub 1.5}A{sub 10.5}Q{sub 5} due to modification of energy level due to presence of Zn{sup 2+} and Al{sup 3+}. The enhancement in PL intensity was observed in Zn{sub 1.5}A{sub 10.5}Q{sub 5} compared to the other composition due to transfer of energy between Zn{sup 2+} and quinolate complex. Optical properties of the prepared materials were evaluated for possible applications in organic light emitting devices (OLED).

Synthesis and characterization of ZrO2-CuO co-doped ceria nanoparticles via chemical precipitation method.

Science.gov (United States)

Viruthagiri, G; Gopinathan, E; Shanmugam, N; Gobi, R

2014-10-15

In the present study, the fluorite cubic phase of bare and ZrO2-CuO co-doped ceria (CeO2) nanoparticles have been synthesized through a simple chemical precipitation method. X-ray diffraction results revealed that average grain sizes of the samples are within 5-6nm range. The functional groups present in the samples were identified by Fourier Transform Infrared Spectroscopy (FTIR) study. Surface area measurement was carried out for the ceria nanoparticles to characterize the surface properties of the synthesized samples. The direct optical cutoff wavelength from DRS analysis was blue-shifted evidently with respect to the bulk material and indicated quantum-size confinement effect in the nanocrystallites. PL spectra revealed the strong and sharp UV emission at 401nm. The surface morphology and the element constitution of the pure and doped nanoparticles were studied by scanning electron microscope fitted with energy dispersive X-ray spectrometer arrangement. The thermal decomposition course was followed using thermo gravimetric and differential thermal analyses (TG-DTA). Copyright © 2014 Elsevier B.V. All rights reserved.

STRONTIUM PRECIPITATION

Science.gov (United States)

McKenzie, T.R.

1960-09-13

A process is given for improving the precipitation of strontium from an aqueous phosphoric-acid-containing solution with nickel or cobalt ferrocyanide by simultaneously precipitating strontium or calcium phosphate. This is accomplished by adding to the ferrocyanide-containing solution calcium or strontium nitrate in a quantity to yield a concentration of from 0.004 to 0.03 and adjusting the pH of the solution to a value of above 8.

Response of soil CO2 efflux to precipitation manipulation in a semiarid grassland.

Science.gov (United States)

Wei, Xiaorong; Zhang, Yanjiang; Liu, Jian; Gao, Hailong; Fan, Jun; Jia, Xiaoxu; Cheng, Jimin; Shao, Mingan; Zhang, Xingchang

2016-07-01

Soil CO2 efflux (SCE) is an important component of ecosystem CO2 exchange and is largely temperature and moisture dependent, providing feedback between C cycling and the climate system. We used a precipitation manipulation experiment to examine the effects of precipitation treatment on SCE and its dependences on soil temperature and moisture in a semiarid grassland. Precipitation manipulation included ambient precipitation, decreased precipitation (-43%), or increased precipitation (+17%). The SCE was measured from July 2013 to December 2014, and CO2 emission during the experimental period was assessed. The response curves of SCE to soil temperature and moisture were analyzed to determine whether the dependence of SCE on soil temperature or moisture varied with precipitation manipulation. The SCE significantly varied seasonally but was not affected by precipitation treatments regardless of season. Increasing precipitation resulted in an upward shift of SCE-temperature response curves and rightward shift of SCE-moisture response curves, while decreasing precipitation resulted in opposite shifts of such response curves. These shifts in the SCE response curves suggested that increasing precipitation strengthened the dependence of SCE on temperature or moisture, and decreasing precipitation weakened such dependences. Such shifts affected the predictions in soil CO2 emissions for different precipitation treatments. When considering such shifts, decreasing or increasing precipitation resulted in 43 or 75% less change, respectively, in CO2 emission compared with changes in emissions predicted without considering such shifts. Furthermore, the effects of shifts in SCE response curves on CO2 emission prediction were greater during the growing than the non-growing season. Copyright © 2016. Published by Elsevier B.V.

Co-precipitation of loperamide hydrochloride and polyethylene glycol using aerosol solvent extraction system

International Nuclear Information System (INIS)

Widjojokusumo, Edward; Youn, Yong-Suk; Lee, Youn-Woo; Veriansyah, Bambang; Tjandrawinata, Raymond Rubianto

2013-01-01

The co-precipitation of loperamide hydrochloride (LPM) and polyethylene glycol (PEG) using aerosol solvent extraction system (ASES) was examined. Scanning electron microscopy - energy dispersive X-ray spectroscopy (SEM-EDS) analysis showed that the co-precipitation was achieved in various LPM-PEG mass ratios with changes in its morphology. In 10-50% PEG mass ratios, angular-shaped particles were formed, whereas in 65-90% PEG mass ratios, irregular-shaped particles were formed. X-ray diffraction (XRD) analysis of the co-precipitates revealed that the LPM retained amorphous structure, while, on the other hand, the PEG retained crystalline structure. Fourier transform infrared (FT-IR) spectra indicated carbonyl function group of LPM and ether function group of PEG appeared in the co-precipitates. Results of a dissolution test showed that the co-precipitates of LPM-PEG had higher dissolution rate compared to that of the raw material and processed LPM with ASES. Taken together, the co-precipitation of LPMPEG was achieved using ASES and higher in its dissolution rate

Research on a pellet co-precipitation micro-filtration process for the treatment of liquid waste containing strontium

International Nuclear Information System (INIS)

Xin Luo; North China Institute of Science and Technology, Beijing; Guanghui Zhang; Xue Wang; Ping Gu

2013-01-01

The chemical precipitation method for radioactive wastewater treatment has the advantages of being simple and cost-effective. However, difficulties with the solid–liquid separation and sludge concentration restrict the application of this method. In this paper, a pellet co-precipitation micro-filtration (PCM) process was studied for treating strontium-containing wastewater on a laboratory scale. The seed was prepared by CaCO 3 powders. Sr 2+ and CO 3 2- were constantly crystallised on the seed surface, with Na 2 CO 3 as the precipitating agent in the pellet reactor. The following membrane separator with the addition of FeCl 3 enhanced the treatment effect. The average strontium concentrations in the raw water and in the effluent were 12.0 and 0.0220 mg/L, respectively. The strontium decontamination factor (DF) increased with the operation time, with an average value of 577. The precipitate particles formed gradually grew larger, with good sedimentation properties. When the experiment was complete, the formed precipitate was separated easily from the liquid phase and directly discharged. The concentration factor (CF) was 1,958. In the PCM process, crystallisation was the main mechanism for strontium removal, with the influent strontium level playing an important role. Membrane pore blockage and cake layer formation could help to further intercept the strontium crystallites. Furthermore, ferric chloride coagulation in the membrane separator also contributed to strontium removal. The PCM process has potential for wider application in the removal of strontium from wastewater. (author)

Dependence of upconversion emission intensity on Yb3+ concentration in Er3+/Yb3+ co-doped flake shaped Y2(MoO4)3 phosphors

International Nuclear Information System (INIS)

Lu Weili; Cheng Lihong; Zhong Haiyang; Sun Jiashi; Wan Jing; Tian Yue; Chen Baojiu

2010-01-01

Yttrium molybdate phosphors with fixed Er 3+ and various Yb 3+ concentrations were synthesized via a co-precipitation method. The crystal structure and the morphology of the phosphor were characterized by means of x-ray diffraction and field-emission scanning electron microscopy. Under 980 nm excitation, red and green upconversion emissions centred at 660, 553 and 530 nm were observed. Quantitative analyses on the dependence of upconversion emission intensity on the working current of a laser diode (LD) indicated that two-photon processes are responsible for both red and green upconversion emissions in both cases of low and high Yb 3+ concentrations. The relationship between the emission intensity ratio of 2 H 11/2 → 4 I 15/2 to 4 S 3/2 → 4 I 15/2 and the working current of the LD was studied for the samples doped with low and high Yb 3+ concentrations. Finally, a set of rate equations was established based on the possible upconversion mechanism, and an empirical formula was proposed to describe the Yb 3+ concentration dependence of upconversion emission intensity; the empirical formula fits well with the experimental data.

Evaluation of the treatability of a winery distillery (vinasse) wastewater by UASB, anoxic-aerobic UF-MBR and chemical precipitation/adsorption.

Science.gov (United States)

Petta, Luigi; De Gisi, Sabino; Casella, Patrizia; Farina, Roberto; Notarnicola, Michele

2017-10-01

A multi-stage pilot-scale treatment cycle consisting of an Upflow Anaerobic Sludge Blanket reactor (UASB) followed by an anoxic-aerobic Ultra Filtration Membrane Bio Reactor (UF-MBR) and a post treatment based on chemical precipitation with lime or adsorption on Granular Activated Carbons (GAC), was applied in order to evaluate the treatment feasibility of a real winery distillery wastewater at laboratory and bench scale. The wastewater was classified as high strength with acidic pH (3.8), and concentrations of 44,600, 254, 604 and 660 mg/l for COD tot , total nitrogen, total phosphorous and phenols, respectively. The UASB reactor was operated at Organic Loading Rates (OLR) in the range 3.0-11.5 kgCOD tot /m 3 /d achieving treatment efficiency up to 97%, with an observed methane production of 340 L of CH 4 /kgCOD. The MBR system was operated with an organic load in the range 0.070-0.185 kgCOD/kgVSS/d, achieving a removal up to 48%, 67% and 65% of the influent COD, total nitrogen and phenols, respectively. The combination of UASB and UF-MBR treatment units was not effective in phosphate and colour removal assigning to further chemical precipitation and adsorption processes, respectively, their complete removal in order to comply with legal standards for wastewater discharge. Subsequently, the optimization of the investigated treatment chain was assessed by applying a chemical precipitation step upstream and downstream the UASB reactor, and a related treatment unit cost assessment is presented in view of a further technological scale-up. Copyright © 2017 Elsevier Ltd. All rights reserved.

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

Preparation and Heat-Treatment of DWPF Simulants With and Without Co-Precipitated Noble Metals

International Nuclear Information System (INIS)

Koopman, David C.:Eibling, Russel E

2005-01-01

The Savannah River National Laboratory is in the process of investigating factors suspected of impacting catalytic hydrogen generation in the Chemical Process Cell of the Defense Waste Processing Facility, DWPF. Noble metal catalyzed hydrogen generation in simulation work constrains the allowable acid addition operating window in DWPF. This constraint potentially impacts washing strategies during sludge batch preparation. It can also influence decisions related to the addition of secondary waste streams to a sludge batch. Noble metals have historically been added as trim chemicals to process simulations. The present study investigated the potential conservatism that might be present from adding the catalytic species as trim chemicals to the final sludge simulant versus co-precipitating the noble metals into the insoluble sludge solids matrix. Parallel preparations of two sludge simulants targeting the composition of Sludge Batch 3 were performed in order to evaluate the impact of the form of noble metals. Identical steps were used except that one simulant had dissolved palladium, rhodium, and ruthenium present during the precipitation of the insoluble solids. Noble metals were trimmed into the other stimulant prior to process tests. Portions of both sludge simulants were held at 97 C for about eight hours to qualitatively simulate the effects of long term storage on particle morphology and speciation. The simulants were used as feeds for Sludge Receipt and Adjustment Tank, SRAT, process simulations. The following conclusions were drawn from the simulant preparation work: (1) The first preparation of a waste slurry simulant with co-precipitated noble metals was successful, based on the data obtained. It appears that 99+% of the noble metals were retained in the simulant. (2) Better control of carbonate, hydroxide, and post-wash trim chemical additions is needed before the new method of simulant preparation will be as reproducible as the old method. (3) The two new

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.

Structural, chemical and magnetic properties of secondary phases in Co-doped ZnO

DEFF Research Database (Denmark)

Ney, A; Kovács, András; Ney, V

2011-01-01

, chemical and magnetic properties of Co-doped ZnO samples. It can be established on a quantitative basis that the superparamagnetic (SPM) behavior observed by integral superconducting quantum interference device magnetometry is not an intrinsic property of the material but stems from precipitations...

A long-term variation of chemical composition in precipitation

International Nuclear Information System (INIS)

Yoshioka, Ryuma; Okimura, Takashi; Okumura, Takenobu

1991-01-01

Precipitation samples are collected at the six localities in the southwestern Japan weekly or monthly over a long period of time (1978-1989) in order to estimate chemical weathering rates and amount of weathered materials through chemical composition in natural waters. Major chemical composition is determined for the precipitation samples. Together with the data available in the literature, the following characteristics are recognized : 1) Most pH values fall in the narrow range of 4.4 to 5.4, 2) Systematic variations in pH values are observed among the precipitation samples of different geologic environments, 3) pH values become almost constant from 1984 to 1989, 4) NO 3 - concentrations gradually decrease to an almost constant value with time, and 5) ΔSO 4 2- concentrations gradually have a tendency to decrease from 1978 to 1985. The mechanism of phenomena described above is also presented. (author)

The use of simultaneous chemical precipitation in modified activated ...

African Journals Online (AJOL)

The use of simultaneous chemical precipitation in modified activated sludge systems exhibiting biological excess phosphate removal: Part 6: Modelling of simultaneous chemical-biological P removal - review of existing models.

Wet chemical synthesis and luminescence in Ca5(PO4)3M:Eu2+ (M = Br, I) phosphors for solid state lighting

Science.gov (United States)

Mungmode, C. D.; Gahane, D. H.; Moharil, S. V.

2018-05-01

A simple wet chemical synthesis of Eu2+ activated Ca5(PO4)3Br and Ca5(PO4)3I phosphors and their photoluminescence is reported. Formation of Ca5(PO4)3Br is confirmed by X-ray diffraction (XRD). Synthesized phosphors are analyzed for photoluminescence (PL) spectrum. A bright blue emission is observed when phosphors are excited by near Ultra Violet (nUV) radiations. Photoluminescence emission spectrum for (Ca0.985Eu0.015)5(PO4)3Br is centered at 457 nm and for (Ca0.985Eu0.015)5(PO4)3 I it peaks at 455 nm when excited by 365 nm near UV radiation. Eu2+ luminescence in Ca5(PO4)3Br is reported for the first time. The phosphors can be efficiently excited by nUV radiations. This shows that phosphors may be used as blue phosphor in pcLED for Solid State Lighting.

Calcium phosphate bioceramics prepared from wet chemically precipitated powders

Directory of Open Access Journals (Sweden)

Kristine Salma

2010-03-01

Full Text Available In this work calcium phosphates were synthesized by modified wet chemical precipitation route. Contrary to the conventional chemical precipitation route calcium hydroxide was homogenized with planetary mill. Milling calcium oxide and water in planetary ball mill as a first step of synthesis provides a highly dispersed calcium hydroxide suspension. The aim of this work was to study the influence of main processing parameters of wet chemical precipitation synthesis product and to control the morphology, phase and functional group composition and, consequently, thermal stability and microstructure of calcium phosphate bioceramics after thermal treatment. The results showed that it is possible to obtain calcium phosphates with different and reproducible phase compositions after thermal processing (hydroxyapatite [HAp], β-tricalcium phosphate [β-TCP] and HAp/β-TCP by modified wet-chemical precipitation route. The β-TCP phase content in sintered bioceramics samples is found to be highly dependent on the changes in technological parameters and it can be controlled with ending pH, synthesis temperature and thermal treatment. Pure, crystalline and highly thermally stable (up to 1300°C HAp bioceramics with homogenous grainy microstructure, grain size up to 200–250 nm and high open porosity can be successfully obtained by powder synthesized at elevated synthesis temperature of 70°C and stabilizing ending pH at 9.

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)

Long-term sustainability of microbial-induced CaCO3 precipitation in aqueous media.

Science.gov (United States)

Gat, Daniella; Ronen, Zeev; Tsesarsky, Michael

2017-10-01

Microbially induced CaCO 3 precipitation (MICP) via urea hydrolysis is an emerging technique for soil amelioration, building materials rehabilitation and pollutants sequestration amongst other various environmental applications. The successful application of MICP requires the sustainability of the precipitated CaCO 3 ; to which the fate of ammonia, the main by-product of ureolysis, is potentially significante. Ammonia volatilization and biological ammonia oxidation both induce a pH decrease, which, in turn, might cause CaCO 3 dissolution. To examine the potential effect of accumulated ammonia on precipitated CaCO 3 , we conducted a long-term MICP batch experiment, using environmental enrichment cultures of ureolytic bacteria. Here we show that CaCO 3 precipitation was completed within 15-27 days, along with a rise in ammonium concentration. Following completion of ureolysis and precipitation, ammonium concentrations decreased, leading to a pH decrease. About 30 days after precipitation was completed, as much as 30% CaCO 3 dissolution, was observed. A two-step model, describing urea hydrolysis followed by the removal of ammonia from the precipitation solution, predicted CaCO 3 dissolution due to ammonia volatilization. We suggest that ureolytic MICP might result in ammonia volatilization, leading to significant CaCO 3 dissolution. These results provide basic insights into the sustainability of ureolytic MICP and should further encourage removal of the accumulated ammonia from the treated site. Copyright © 2017 Elsevier Ltd. All rights reserved.

Effects of Calcium Source on Biochemical Properties of Microbial CaCO3 Precipitation.

Science.gov (United States)

Xu, Jing; Du, Yali; Jiang, Zhengwu; She, Anming

2015-01-01

The biochemical properties of CaCO3 precipitation induced by Sporosarcina pasteurii, an ureolytic type microorganism, were investigated. Effects of calcium source on the precipitation process were examined, since calcium source plays a key role in microbiologically induced mineralization. Regardless of the calcium source type, three distinct stages in the precipitation process were identified by Ca(2+), NH4 (+), pH and cell density monitoring. Compared with stage 1 and 3, stage 2 was considered as the most critical part since biotic CaCO3 precipitation occurs during this stage. Kinetics studies showed that the microbial CaCO3 precipitation rate for calcium lactate was over twice of that for calcium nitrate, indicating that calcium lactate is more beneficial for the cell activity, which in turn determines urease production and CaCO3 precipitation. X-ray diffraction analysis confirmed the CaCO3 crystal as calcite, although scanning electron microscopy revealed a difference in crystal size and morphology if calcium source was different. The findings of this paper further suggest a promising application of microbiologically induced CaCO3 precipitation in remediation of surface and cracks of porous media, e.g., cement-based composites, particularly by using organic source of calcium lactate.

A Strategy for Synthesizing CaZnOS:Eu{sup 2+} Phosphor and Comparison of Optical Properties with CaS:Eu{sup 2+}

Energy Technology Data Exchange (ETDEWEB)

Qiu, Zhongxian; Rong, Chunying; Zhou, Wenli; Zhang, Jilin; Li, Chengzhi; Yu, Liping; Liu, Shubin; Lian, Shixun, E-mail: shixunlian@gmail.com

2014-01-15

Graphical abstract: Pure-phase CaZnOS:Eu{sup 2+},Ce{sup 3+}phosphor with good chemical and thermal stability can be synthesized by co-doping with Ce{sup 3+} as deoxidizer rather than reduction atmosphere. The broad bluish-green excitation and broad red emission show it is a better phosphor than CaS:Eu{sup 2+} for white LED and for sunlight harvesting of plants. -- Highlights: • Pure-phase phosphor CaZnOS:Eu{sup 2+} was synthesized by co-doping with Ce{sup 3+} as deoxidizer. • Energy transfer mechanism from Ce{sup 3+} to Eu{sup 2+} in CaZnOS host is proposed. • CaZnOS:Eu{sup 2+}, Ce{sup 3+} phosphor has good chemical and thermal stability performance. • The similarities and differences between CaZnOS:Eu{sup 2+} and CaS:Eu{sup 2+} were analyzed. • The green excitation and red emission show superior solar harvesting for plants. -- Abstract: The red-emitting phosphor CaZnOS:Eu{sup 2+} was synthesized from CaCO{sub 3}, ZnS, Eu{sub 2}O{sub 3} and CeCl{sub 3} by controlling the sintering condition. It was found that Ce{sup 3+} ions can play a role of reductant to contribute to the formation of Eu{sup 2+} in CaZnOS matrix under inert protective atmosphere. While the gas flow changed to H{sub 2}/N{sub 2}, the product turned to CaS easily. XRD, photoluminescence spectra, UV–vis and IR absorption spectra were evaluated to investigate the origin of the distinctions of the optical properties and stabilities between the two divalent europium ions doped phosphors CaZnOS:Eu{sup 2+} and CaS:Eu{sup 2+}. The similarities and differences between them were analyzed.

Supercritical antisolvent co-precipitation of rifampicin and ethyl cellulose

CSIR Research Space (South Africa)

Djerafi, R

2017-05-01

Full Text Available . Using the solvent mixture, co-precipitates with particle sizes ranging between 190 and 230 nm were obtained with drug loading and drug precipitation yield from respectively 8.5 to 38.5 and 42.4 to 77.2% when decreasing the ethyl cellulose...

Photochemically induced deposition of protective alumina coatings onto UV emitting phosphors for Xe excimer discharge lamps

International Nuclear Information System (INIS)

Broxtermann, Mike; Jüstel, Thomas

2016-01-01

Highlights: • A UV-reactor for the pH induced precipitation of inorganic material is described. • The photolysis of Azide (N_3"−) leads to a steady pH increase used for precipitation. • A UV induced Al(OH)_3 precipitation is used to craft Al_2O_3 coatings onto YPO_4:Bi. • The influence of Al_2O_3 coated onto YPO_4:Bi with different thicknesses is discussed. • SEM, VUV-spectroscopy and ESA measurements were performed on Al_2O_3 coated samples. - Abstract: This work concerns the particle coating of the UV-C emitting phosphor YPO_4:Bi, targeting a stability enhancement of the phosphor material for Xe excimer lamp operation. To this end, the material is coated by the wide band gap material Al_2O_3. In order to obtain a thin and homogeneous coating layer, a novel process based on the photochemical cleavage of NaN_3 in water was developed. This results in a slow and continuous enhancement of the pH value due to ongoing NaOH formation, which results in the precipitation of Al(OH)_3 from an Al_2(SO_4)_3 _× 18H_2O solution. It turned out that the obtained particle coatings are of much better quality, i.e. homogeneity, compared to coatings made from a wet-chemical homogeneous precipitation process. The morphology and electrochemical properties of Al_2O_3 coated YPO_4:Bi are discussed on the basis of optical spectroscopy, ESA measurements, and SEM/EDX investigations.

Characterization of ZnS nanoparticles synthesized by co-precipitation method

International Nuclear Information System (INIS)

Iranmanesh Parvaneh; Nourzpoor Mohsen; Saeednia Samira

2015-01-01

ZnS nanoparticles are prepared by homogeneous chemical co-precipitation method using EDTA as a stabilizer and capping agent. The structural, morphological, and optical properties of as-synthesized nanoparticles are investigated using x-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, ultraviolet-visible (UV-Vis) absorption, and photoluminescence spectroscopy. The x-ray diffraction pattern exhibits a zinc-blended crystal structure at room temperature. The average particle size of the nanoparticles from the scanning electron microscopy image is about 50 nm. The ultraviolet absorption spectrum shows the blue shift in the band gap due to the quantum confinement effect. The photoluminescence spectrum of ZnS nanoparticles shows a blue visible spectrum. (paper)

co-removal with nucleated Cu(II) precipitation in continuous-flow ...

African Journals Online (AJOL)

A compact nucleated precipitation technology using two fluidised sand columns in series was developed to pretreat model metal-plating wastewater containing high concentrations of Cu(II) and Cr(VI). Since either Cu(II) precipitation or Cr(VI) co-removal with Cu(II) precipitation was found to be highly pH dependent in batch ...

Surface chemical reactions during electron beam irradiation of nanocrystalline CaS:Ce3+ phosphor

International Nuclear Information System (INIS)

Kumar, Vinay; Pitale, Shreyas S.; Nagpure, I. M.; Coetsee, E.; Ntwaeaborwa, O. M.; Terblans, J. J.; Swart, H. C.; Mishra, Varun

2010-01-01

The effects of accelerating voltage (0.5-5 keV) on the green cathodoluminescence (CL) of CaS:Ce 3+ nanocrystalline powder phosphors is reported. An increase in the CL intensity was observed from the powders when the accelerating voltage was varied from 0.5 to 5 keV, which is a relevant property for a phosphor to be used in field emission displays (FEDs). The CL degradation induced by prolonged electron beam irradiation was analyzed using CL spectroscopy, x-ray photoelectron spectroscopy (XPS) and Auger electron spectroscopy (AES). The AES data showed the decrease in the S peak intensity and an increase in the O peak intensity during electron bombardment. The CL intensity was found to decrease to 30% of its original intensity after about 50 C/cm 2 . XPS was used to study the chemical composition of the CaS:Ce 3+ nanophosphor before and after degradation. The XPS data confirms that a nonluminescent CaSO 4 layer has formed on the surface during the degradation process, which may partially be responsible for the CL degradation. The electron stimulated surface chemical reaction mechanism was used to explain the effects of S desorption and the formation of the nonluminescent CaSO 4 layer on the surface.

Luminescence properties of Ce{sup 3+} and Tb{sup 3+} co-activated ZnAl{sub 2}O{sub 4} phosphor

Energy Technology Data Exchange (ETDEWEB)

Tshabalala, K.G. [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa); Cho, S.-H.; Park, J.-K. [Nano-Materials Center, Korea Institute of Science and Technology, Cheongryang, Seoul 130-650 (Korea, Republic of); Pitale, Shreyas S.; Nagpure, I.M.; Kroon, R.E.; Swart, H.C. [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa); Ntwaeaborwa, O.M., E-mail: ntwaeab@ufs.ac.za [Department of Physics, University of the Free State, Bloemfontein, ZA 9300 (South Africa)

2012-05-15

In this study, a solution combustion method was used to prepare green emitting Ce{sup 3+}-Tb{sup 3+} co-activated ZnAl{sub 2}O{sub 4} phosphor. The samples were annealed at 700 Degree-Sign C in air or hydrogen atmosphere to improve their crystallinity and optical properties. X-ray diffraction study confirmed that both as-prepared and post-preparation annealed samples crystallized in the well known cubic spinel structure of ZnAl{sub 2}O{sub 4}. An agglomeration of irregular platelet-like particles whose surfaces were encrusted with smaller spheroidal particles was confirmed by scanning electron microscopy (SEM). The fluorescence data collected from the annealed samples with different concentrations of Ce{sup 3+} and Tb{sup 3+} show the enhanced green emission at 543 nm associated with {sup 5}D{sub 4}{yields}{sup 7}F{sub 5} transitions of Tb{sup 3+}. The enhancement was attributed to energy transfer from Ce{sup 3+} to Tb{sup 3+}. Possible mechanism of energy transfer via a down conversion process is discussed. Furthermore, cathodoluminescence (CL) intensity degradation of this phosphor was also investigated and the degradation data suggest that the material was chemically stable and the CL intensity was also stable after 10 h of irradiation by a beam of high energy electrons.

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.

Effectiveness of Arsenic Co-Precipitation with Fe-Al Hydroxides for Treatment of Contaminated Water

Directory of Open Access Journals (Sweden)

Jaime Wilson Vargas de Mello

2018-03-01

Full Text Available ABSTRACT Wastewater treatment is a challenging problem faced by the mining industry, especially when mine effluents include acid mine drainage with elevated arsenic levels. Iron (hydroxides are known to be effective in removal of As from wastewater, and although the resulting compounds are relatively unstable, the presence of structural Al enhances their stability, particularly under reducing conditions. The purpose of this study was to assess the effectiveness of Al-Fe (hydroxide co-precipitates for the removal of As from wastewater and to assess the chemical stability of the products. Different Al-Fe (hydroxides were synthesized at room temperature from ferrous and aluminum salts using three different Fe:Al molar ratios (1:0.0, 1:0.3, and 1:0.7 and aged for 90 days (sulfate experiments or 120 days (chloride experiments in the presence of arsenic. At the end of the aging periods, the precipitated sludges were dried and characterized in order to evaluate their stability and therefore potential As mobility. All treatments were effective in reducing As levels in the water to below 10 µg L-1, but the presence of Al impaired the effectiveness of the treatment. Aluminum decreased the chemical stability of the precipitated sludge and hence its ability to retain As under natural environmental conditions.

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.

Low lag luminescent phosphors

International Nuclear Information System (INIS)

1976-01-01

The addition of potassium or rubidium salts to europium-activated fluorohalide phosphors produces X-ray screens with low lag, even at very low europium concentrations. The chemical preparation and afterglow test results are described

Co-precipitation and solubility studies of cesium, potassium and sodium tetraphenylborate

International Nuclear Information System (INIS)

Peterson, R.A.

1999-01-01

This report contains the results from a study requested by High Level Waste Division on the co-precipitation and solubility of cesium, potassium, and sodium tetraphenylborate. Co-precipitation of cesium (Cs), potassium (K), and sodium (Na) tetraphenylborate (TPB) helps determine the efficiency of reagent usage in the Small Tank Precipitation Process. This process uses NaTPB to remove cesium from waste by means of precipitation. Previous studies by McCabe suggested that if the sodium ion concentration [Na+] increased the rate at which cesium tetraphenylborate (KTPB) in the presence of high [Na+] (∼5M) appears to produce a mixed solid phase composed of NaTPB and KTPB together in the crystal lattice

Synthesis and thermoluminescence characterization of Na6Mg(SO4)4:RE (RE = Ce, Tb) phosphors

International Nuclear Information System (INIS)

Kore, Bhushan P.; Dhoble, N.S.; Dhoble, S.J.

2014-01-01

Thermoluminescence (TL) properties of sulfate-based phosphors activated by different rare earths have received tremendous attention to the field of radiation dosimetry. Those TL materials based on CaSO 4 have been widely applied for medical and environmental dosimetry. Taking this fact into account we have synthesized Na 6 Mg(SO 4 ) 4 doped with Ce and Tb by wet chemical method. The prepared phosphor was characterized by XRD, FTIR, photoluminescence (PL) and thermoluminescence. For TL study, the phosphor is irradiated with γ-rays from 60 Co source. For studying luminescence properties, the prepared phosphor was annealed at different temperatures and effects of these annealing temperatures on Na 6 Mg(SO 4 ) 4 samples are investigated and quantified. The changes in the glow curve and PL emission spectrum are also investigated as a function of annealing temperature and the annealing temperature was optimized. For calculation of trapping parameters various methods such as peak shape (PS) method, initial rise (IR) method, various heating rate (VHR) method, and computerized glow curve deconvolution (CGCD) are employed. - Highlights: • Na 6 Mg(SO 4 ) 4 phosphor was successfully prepared by wet chemical method. • Effect of annealing temperatures on PL and TL properties has been studied. • Different trap analysis methods were used for calculating the trapping parameters. • Effect of these methods on activation energies were investigated in detail

A laboratory study of ikaite (CaCO3·6H2O) precipitation as a function of pH, salinity, temperature and phosphate concentration

OpenAIRE

Hu, Yu-Bin; Wolf-Gladrow, Dieter A.; Dieckmann, Gerhard S.; Völker, Christoph; Nehrke, Gernot

2014-01-01

Ikaite (CaCO3·6H2O) has only recently been discovered in sea ice, in a study that also provided first direct evidence of CaCO3 precipitation in sea ice. However, little is as yet known about the impact of physico-chemical processes on ikaite precipitation in sea ice. Our study focused on how the changes in pH, salinity, temperature and phosphate (PO4) concentration affect the precipitation of ikaite. Experiments were set up at pH from 8.5 to 10.0, salinities from 0 to 105 (in both artificial ...

Photoluminescence and magnetic properties of Fe-doped ZnS nano-particles synthesized by chemical co-precipitation

Energy Technology Data Exchange (ETDEWEB)

Nie Eryong; Liu Donglai; Zhang Yunsen; Bai Xue; Yi Liang; Jin Yong; Jiao Zhifeng [School of Materials Science and Engineering, Sichuan University, Chengdu 610064, Sichuan (China); Sun Xiaosong, E-mail: sunxs@scu.edu.cn [School of Materials Science and Engineering, Sichuan University, Chengdu 610064, Sichuan (China)

2011-08-15

This paper is focusing on the synthesis of Zn{sub 1-x}Fe{sub x}S nano-particles with x = 0, 0.1 and 0.2 by chemical co-precipitation method, the prepared of which are characterized by XRD, EDS, TEM, PL, magnetization versus field behavior and M-T curve. In the XRD patterns, Zn{sub 1-x}Fe{sub x}S nano-particles are shown of cubic zinc blende structure, and the broadening diffraction peaks consistent with the small-size characteristic of nano-materials. The diameter of nano-particles is between 3.3 and 5.5 nm according to the HR-TEM images. The EDS data confirm the existence of Fe ions in Fe-doped ZnS nanoparticles. There we found that Fe-doping did not import new energy bands or defect states, but reduced the intensity of PL peaks. The magnetization versus field behaviors were illustrated by the M-H curves at both 5 K and 300 K, respectively, where no remanence or coercive force was observed. This phenomenon indicates that the Zn{sub 1-x}Fe{sub x}S (x = 0.1) nano-particles are superparamagnetic. The zero-field-cooled (ZFC) and field-cooled (FC) magnetization curves further reveal that the blocking temperature (T{sub B}) of the superparamagnetic behavior might be below 5 K.

Synthesis and cathodoluminescent properties of Y2SiO5:Tb3+ phosphors prepared from uniform precursor

International Nuclear Information System (INIS)

Fan Deyong; Yang Sen; Wang Jieqiong; Zheng Aqun; Song Xiaoping; Yu Demei

2012-01-01

The luminescent properties of phosphors are sensitive to the size of phosphor particles. The commercial Y 2 SiO 5 :Tb 3+ phosphors usually show relatively larger particle size (5–10 μm) due to the irregular morphology of rare earth oxide precursor and thus degrade the luminescent properties. In this paper, we report the Y 2 SiO 5 :Tb 3+ phosphors synthesized from the uniform Tb-doped Y 2 O 3 precursor by a homogeneous precipitation method. Compared with the commercial phosphors, the obtained Y 2 SiO 5 :Tb 3+ phosphors manifest the uniform morphology with much smaller particles distributing from 0.8 μm to 1.9 μm. Consequently, the cathodoluminescent intensity under low excitation voltage (1–5 kV) was increased, demonstrating a strong green emission with a dominant wavelength of 545 nm. Our results indicate an effective way to develop the high-quality phosphors for field emission display. - Highlights: ► The Y 2 SiO 5 :Tb 3+ phosphors are synthesized by a homogeneous precipitation method. ► They manifest the uniform morphology with much smaller particles than commercial one. ► The corresponding cathodoluminescent intensity of green emission is greatly enhanced. ► Our results indicate an effective way to develop the high-quality phosphors for FED.

UV and VUV characteristics of (YGd)2O3:Eu phosphor particles prepared by spray pyrolysis from polymeric precursors

International Nuclear Information System (INIS)

Kim, E.J.; Kang, Y.C.; Park, H.D.; Ryu, S.K.

2003-01-01

Red-emitting (YGd) 2 O 3 :Eu phosphor particles, with high luminescence efficiency under vacuum ultraviolet (VUV) and ultraviolet (UV) excitation, were prepared by a large-scale spray pyrolysis process. To control the morphology of phosphor particles under severe preparation conditions, spray solution with polymeric precursors were introduced in spray pyrolysis. The prepared (YGd) 2 O 3 :Eu phosphor particles had spherical shape and filled morphology even after post-treatment irrespective of Gd/Y ratio. In the case of solution with polymeric precursors, long polymeric chains formed by esterification reaction in a hot tubular reactor; the droplets turned into viscous gel, which retarded the precipitation of nitrate salts and promoted the volume precipitation of droplets. The brightness of (YGd) 2 O 3 :Eu phosphor particles increased with increasing gadolinium content, and the Gd 2 O 3 :Eu phosphor had the highest luminescence intensity under UV and VUV excitation. The maximum peak intensity of Gd 2 O 3 :Eu phosphor particles under UV and VUV were 118 and 110% of the commercial Y 2 O 3 :Eu phosphor particles, respectively

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)

Procedure to use phosphogypsum industrial waste for mineral CO2 sequestration

International Nuclear Information System (INIS)

Cárdenas-Escudero, C.; Morales-Flórez, V.; Pérez-López, R.; Santos, A.; Esquivias, L.

2011-01-01

Highlights: ► Phosphogypsum wastes are proposed to reduce CO 2 greenhouse gas emissions. ► Phosphogypsum dissolution with NaOH results in Ca(OH) 2 precipitation and Na 2 SO 4 . ► Aqueous carbonation of Ca(OH) 2 with CO 2 results in the CaCO 3 precipitation. ► Metals contained in the phosphogypsum are transferred to the final calcite. ► Applications of CaCO 3 and Na 2 SiO 4 by-products are proposed to improve viability. - Abstract: Industrial wet phosphoric acid production in Huelva (SW Spain) has led to the controversial stockpiling of waste phosphogypsum by-products, resulting in the release of significant quantities of toxic impurities in salt marshes in the Tinto river estuary. In the framework of the fight against global climate change and the effort to reduce carbon dioxide emissions, a simple and efficient procedure for CO 2 mineral sequestration is presented in this work, using phosphogypsum waste as a calcium source. Our results demonstrate the high efficiency of portlandite precipitation by phosphogypsum dissolution using an alkaline soda solution. Carbonation experiments performed at ambient pressure and temperature resulted in total conversion of the portlandite into carbonate. The fate of trace elements present in the phosphogypsum waste was also investigated, and trace impurities were found to be completely transferred to the final calcite. We believe that the procedure proposed here should be considered not only as a solution for reducing old stockpiles of phosphogypsum wastes, but also for future phosphoric acid and other gypsum-producing industrial processes, resulting in more sustainable production.

γ' Precipitation Study of a Co-Ni-Based Alloy

Science.gov (United States)

Locq, D.; Martin, M.; Ramusat, C.; Fossard, F.; Perrut, M.

2018-05-01

A Co-Ni-based alloy strengthened by γ'-(L12) precipitates was utilized to investigate the precipitation evolution after various cooling rates and several aging conditions. In this study, the precipitate size and volume fraction have been studied via scanning electron microscopy and transmission electron microscopy. The influence of the precipitation evolution was measured via microhardness tests. The cooling rate study shows a more sluggish γ' precipitation reaction compared to that observed in a Ni-based superalloy. Following a rapid cooling rate, the application of appropriate double aging treatments allows for the increase of the γ' volume fraction as well as the control of the size and distribution of the precipitates. The highest hardness values reach those measured on supersolvus cast and wrought Ni-based superalloys. The observed γ' precipitation behavior should have implications for the production, the heat treatment, the welding, or the additive manufacturing of this new class of high-temperature materials.

Precipitation Coating of Monazite on Woven Ceramic Fibers: 1. Feasibility (Postprint)

Science.gov (United States)

2007-02-01

08 Aug 2006. Paper contains color . 14. ABSTRACT Monazite coatings were deposited on woven cloths and tows of NextelTM 610 fibers by heterogeneous...by dissolving concentrated phosphoric acid ( Fish - er Scientific Co., Pittsburgh, PA) or a combination of lantha- num nitrate (Aldrich Chemical Co...Boccaccini, P. Karapappas, J. M. Marijuan, and C. Kaya, ‘‘ TiO2 Coat- ings on Silicon Carbide Fiber Substrates by Electrophoretic Deposition,’’ J.Mater. Sci

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.)

Nanoscale co-precipitation and mechanical properties of a high-strength low-carbon steel

International Nuclear Information System (INIS)

Mulholland, Michael D.; Seidman, David N.

2011-01-01

Nanoscale co-precipitation in a novel high-strength low-carbon steel is studied in detail after isothermal aging. Atom-probe tomography is utilized to quantify the co-precipitation of co-located Cu precipitates and M 2 C (M is any combination of Cr, Mo, Fe, or Ti) carbide strengthening precipitates. Coarsening of Cu precipitates is offset by the nucleation and growth of M 2 C carbide precipitate, resulting in the maintenance of a yield strength of 1047 ± 7 MPa (152 ± 1 ksi) for as long as 320 h of aging time at 450 deg. C. Impact energies of 153 J (113 ± 6 ft-lb) and 144 J (106 ± 2 ft-lb) are measured at -30 deg. C and -60 deg. C, respectively. The co-location of Cu and M 2 C carbide precipitates results in non-stationary-state coarsening of the Cu precipitates. Synchrotron-source X-ray diffraction studies reveal that the measured 33% increase in impact toughness after aging for 80 h at 450 deg. C is due to dissolution of cementite, Fe 3 C, which is the source of carbon for the nucleation and growth of M 2 C carbide precipitates. Less than 1 vol.% austenite is observed for aging treatments at temperatures less than 600 deg. C, suggesting that transformation-induced plasticity does not play a significant role in the toughness of specimens aged at temperatures less than 600 deg. C. Aging treatments at temperatures greater than 600 deg. C produce more austenite, in the range 2-7%, but at the expense of yield strength.

The Influence of Phosphor and Binder Chemistry on the Aging Characteristics of Remote Phosphor Products

Energy Technology Data Exchange (ETDEWEB)

Davis, Lynn; Yaga, Robert; Lamvik, Michael; Mills, Karmann; Fletcher, B.

2017-06-30

The influence of phosphor and binder layer chemistries on the lumen maintenance and color stability of remote phosphor disks were examined using wet high-temperature operational lifetime testing (WHTOL). As part of the experimental matrix, two different correlated color temperature (CCT) values, 2700 K and 5000 K, were studied and each had a different binder chemistry. The 2700 K samples used a urethane binder whereas the 5000 K samples used an acrylate binder. Experimental conditions were chosen to enable study of the binder and phosphor chemistries and to minimize photo-oxidation of the polycarbonate substrate. Under the more severe WHTOL conditions of 85°C and 85% relative humidity (RH), absorption in the binder layer significantly reduced luminous flux and produced a blue color shift. The milder WHTOL conditions of 75°C and 75% RH, resulted in chemical changes in the binder layer that may alter its index of refraction. As a result, lumen maintenance remained high, but a slight yellow shift was found. The aging of remote phosphor products provides insights into the impact of materials on the performance of phosphors in an LED lighting system.

Treatment alternatives of liquid radioactive waste containing uranium in phosphoric acid

International Nuclear Information System (INIS)

Bustamante Escobedo, Mauricio

2003-01-01

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

Re-processing CRT phosphors for mercury-free applications

International Nuclear Information System (INIS)

Dexpert-Ghys, Jeannette; Regnier, Sophie; Canac, Sophie; Beaudette, Tristan; Guillot, Philippe; Caillier, Bruno; Mauricot, Robert; Navarro, Julien; Sekhri, Salem

2009-01-01

This study is part of an operation in the framework of treatment and revalorization of IEEE (Informatics, Electronics and related) wastes. It aims to recover the active phosphors in cathode ray tubes (CRTs) and to re-cycle these powders by appropriate treatments as phosphors for mercury-free applications such as plasma display panels, flat lamps, advertising and lighting. The studied waste comes from a large panel of CRTs from any supplier. Several thermo-chemical treatments have been investigated. The removal of zinc sulfide-based phosphors and the recovery of a red phosphor Y 2 O 3 :Eu 3+ has been achieved by one (basic attack) route. The photoluminescence efficiency under VUV excitation of the obtained powders is at most 30% that of a commercial phosphor. The second route (acid attack) appears less promising. It has been established that silicate-based impurities could prevent isolating the yttrium based phosphor.

Re-processing CRT phosphors for mercury-free applications

Energy Technology Data Exchange (ETDEWEB)

Dexpert-Ghys, Jeannette, E-mail: jdexpert@cemes.f [CEMES, 29 rue Jeanne Marvig, BP 94347, 31055 Toulouse cedex 4 (France); Regnier, Sophie; Canac, Sophie [ICAM, 75 avenue de Grande Bretagne, 31300 Toulouse (France); Beaudette, Tristan; Guillot, Philippe; Caillier, Bruno [DPHE, Universite Jean Francois Champollion, place de Verdun, 81012 Albi cedex 9 (France); Mauricot, Robert; Navarro, Julien [CEMES, 29 rue Jeanne Marvig, BP 94347, 31055 Toulouse cedex 4 (France); Sekhri, Salem [ENVOI, Cheminement Glueck, 31100 Toulouse (France)

2009-12-15

This study is part of an operation in the framework of treatment and revalorization of IEEE (Informatics, Electronics and related) wastes. It aims to recover the active phosphors in cathode ray tubes (CRTs) and to re-cycle these powders by appropriate treatments as phosphors for mercury-free applications such as plasma display panels, flat lamps, advertising and lighting. The studied waste comes from a large panel of CRTs from any supplier. Several thermo-chemical treatments have been investigated. The removal of zinc sulfide-based phosphors and the recovery of a red phosphor Y{sub 2}O{sub 3}:Eu{sup 3+} has been achieved by one (basic attack) route. The photoluminescence efficiency under VUV excitation of the obtained powders is at most 30% that of a commercial phosphor. The second route (acid attack) appears less promising. It has been established that silicate-based impurities could prevent isolating the yttrium based phosphor.

The magnetic and colloidal properties of CoFe2O4 nanoparticles synthesized by co-precipitation.

Science.gov (United States)

Gyergyek, Sašo; Drofenik, Miha; Makovec, Darko

2014-01-01

Magnetic CoFe(2)O(4) nanoparticles were synthesized by co-precipitation at 80 °C. This co-precipitation was achieved by the rapid addition of a strong base to an aqueous solution of cations. The investigation of the samples that were quenched at different times after the addition of the base, using transmission electron microscopy (TEM) coupled with energy-dispersive X-ray spectroscopy (EDXS) and X-ray powder diffractometry, revealed the formation of a Co-deficient amorphous phase and Co(OH)(2), which rapidly reacted to form small CoFe(2)O(4) nanoparticles. The nanoparticles grew with the time of aging at elevated temperature. The colloidal suspensions of the nanoparticles were prepared in both an aqueous medium and in a non-polar organic medium, with the adsorption of citric acid and ricinoleic acid on the nanoparticles, respectively. The measurements of the room-temperature magnetization revealed the ferrimagnetic state of the CoFe(2)O(4) nanoparticles, while their suspensions displayed superparamagnetic behaviour.

Oleic-acid-coated CoFe2O4 nanoparticles synthesized by co-precipitation and hydrothermal synthesis

International Nuclear Information System (INIS)

Gyergyek, Sašo; Drofenik, Miha; Makovec, Darko

2012-01-01

Highlights: ► Synthesis of oleic-acid-coated CoFe 2 O 4 nanoparticles from an aqueous solution. ► During the co-precipitation of Co 2+ /Fe 3+ single-phase spinel forms. ► During the co-precipitation of Co 2+ /Fe 2+ , feroxyhyte forms in addition to spinel. ► Oleic acid increases the spinel formation temperature and limits particle growth. ► Colloidal suspensions of ferrimagnetic CoFe 2 O 4 were prepared. - Abstract: Oleic-acid-coated CoFe 2 O 4 nanoparticles were synthesized by co-precipitation and hydrothermal synthesis. The coprecipitation of the nanoparticles was achieved by the rapid addition of a strong base to an aqueous solution of cations in the presence of the oleic acid surfactant, or without this additive. The nanoparticles were also synthesized by a hydrothermal treatment of suspensions of the precipitates, coprecipitated at room temperature in the presence of the oleic acid, or without it. The influence of the synthesis conditions, such as the valence state of the iron cation in the starting aqueous solution, the temperature of the treatment and the presence of oleic acid, on the particles size was systematically studied. X-ray powder diffractometry (XRD) and transmission electron microscopy (TEM) coupled with energy-dispersive X-ray spectroscopy (EDS) revealed that, although spinel forms at room temperature, a substantial amount of Co was incorporated within the secondary, feroxyhyte-like phase when the iron cation was in the 2+ state. In contrast, when iron was in the 3+ state, the spinel forms at elevated temperatures of approximately 60 °C. The presence of the oleic acid further increased the formation temperature for the stoichiometric spinel. Moreover, the oleic acid impeded the particles’ growth and enabled the preparation of colloidal suspensions of the nanoparticles in non-polar organic solvents. The nanoparticles’ size was successfully controlled by the temperature of the synthesis in the region where superparamagnetism

Synthesis and characterization of polyethylene glycol (PEG) coated Fe3O4 nanoparticles by chemical co-precipitation method for biomedical applications.

Science.gov (United States)

Anbarasu, M; Anandan, M; Chinnasamy, E; Gopinath, V; Balamurugan, K

2015-01-25

Polyethylene glycol (PEG) coated Fe3O4 nanoparticles were synthesized by chemical co-precipitation method. With polyethylene glycol (PEG) as a stabilizer and dispersant. The X-ray diffraction and selected area electron diffraction (SAED) results show that the cubic inverse spinel structure of pure phase polycrystalline Fe3O4 was obtained. The scanning electron microscopy (SEM) and field emission transmission electron microscopy (FE-TEM) results exhibited that the resulted Fe3O4 nanoparticles were roughly spherical in shape with narrow size distribution and homogenous shape. Fourier transform infrared spectroscopy (FT-IR) results suggested that PEG indicated with Fe3O4 via its carbonyl groups. Results of vibrating sample magnetometer (VSM) indicated that the prepared Fe3O4 nanoparticles exhibit superparamagnetic behavior and high saturation magnetization at room temperature. Such Fe3O4 nanoparticles with favorable size and tunable magnetic properties are promising biomedical applications. Copyright © 2014. Published by Elsevier B.V.

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

Impact of elevated CO_2 concentrations on carbonate mineral precipitation ability of sulfate-reducing bacteria and implications for CO_2 sequestration

International Nuclear Information System (INIS)

Paul, Varun G.; Wronkiewicz, David J.; Mormile, Melanie R.

2017-01-01

Interest in anthropogenic CO_2 release and associated global climatic change has prompted numerous laboratory-scale and commercial efforts focused on capturing, sequestering or utilizing CO_2 in the subsurface. Known carbonate mineral precipitating microorganisms, such as the anaerobic sulfate-reducing bacteria (SRB), could enhance the rate of conversion of CO_2 into solid minerals and thereby improve long-term storage of captured gasses. The ability of SRB to induce carbonate mineral precipitation, when exposed to atmospheric and elevated pCO_2, was investigated in laboratory scale tests with bacteria from organic-rich sediments collected from hypersaline Lake Estancia, New Mexico. The enriched SRB culture was inoculated in continuous gas flow and batch reactors under variable headspace pCO_2 (0.0059 psi to 20 psi). Solution pH, redox conditions, sulfide, calcium and magnesium concentrations were monitored in the reactors. Those reactors containing SRB that were exposed to pCO_2 of 14.7 psi or less showed Mg-calcite precipitation. Reactors exposed to 20 psi pCO_2 did not exhibit any carbonate mineralization, likely due to the inhibition of bacterial metabolism caused by the high levels of CO_2. Hydrogen, lactate and formate served as suitable electron donors for the SRB metabolism and related carbonate mineralization. Carbon isotopic studies confirmed that ∼53% of carbon in the precipitated carbonate minerals was derived from the CO_2 headspace, with the remaining carbon being derived from the organic electron donors, and the bicarbonate ions available in the liquid medium. The ability of halotolerant SRB to induce the precipitation of carbonate minerals can potentially be applied to the long-term storage of anthropogenic CO_2 in saline aquifers and other ideal subsurface rock units by converting the gas into solid immobile phases. - Highlights: • SRB under study are capable of precipitating calcite up to 14.7 psi pCO_2. • At 20 psi pCO_2, bacterial activity

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.

Comparison of the properties of simulated synroc synthesized by sol-gel and a novel co - precipitation method

International Nuclear Information System (INIS)

Potdar, H.S.; Vijayanand, S.; Khaja Mohaideen, K.; Joy, P.A.; Raja Madhavan, R.; Kutty, K.V.G.; Ambashta, R.D.; Wattal, P.K.

2009-01-01

Synroc is a multiphase dense titanate based ceramic designed for the incorporation of high-level waste (HLW) from the reprocessing of spent nuclear fuel. Synroc or synthetic rock consists of four main titanate phases - zirconolite (CaZrTi 2 O 7 ), hollandite (BaAlO 2 Ti 6 O 16 ), perovskite (CaTiO 3 ) and rutile (TiO 2 ), with the matrix composition as shown in Table 1. It is known that these phases have the capacity to incorporate most of the elements into their crystal structures which are present in the HLW derived from the reprocessing of spent nuclear fuel from power reactors. Synroc is considered as the most effective and durable means of immobilising various forms of high-level radioactive wastes for disposal. Synroc is also considered as a low-risk, tailored waste form, offering higher waste loading and over all cost savings. Simulated synroc precursor powders are typically produced by advanced wet chemical methods such as alkoxide hydrolysis and sol-gel routes. These routes were developed to produce powders with well defined physical and chemical characteristics such as correct chemical composition, high degree of homogeneity, reactivity and readily densifiable material to 99% of theoretical density during hot isostatic pressing. However, the reported alkoxide hydrolysis and hydroxide routes suffer from several disadvantages such as use of large quantities of organic solvents and their disposal as effluent, difficulty in maintaining exact chemical composition, use of costly alkoxide precursors which are moisture sensitive and require critical processing conditions to control their rate of hydrolysis, etc. In the present work we report a comparative study the characteristics of synroc-C (14% waste loading) powders and sintered pellets synthesized by the known alkoxide hydrolysis method and a simple chemical co-precipitation route developed by us. The advantages of the co-precipitation route are its simplicity, ease of handling and utilization of cheaper raw

Precipitation of hydrated Mg carbonate with the aid of carbonic anhydrase for CO2 sequestration

Science.gov (United States)

Power, I. M.; Harrison, A. L.; Dipple, G. M.

2011-12-01

Strategies for sequestering CO2 directly from the atmosphere are likely required to achieve the desired reduction in CO2 concentration and avoid the most damaging effects of climate change [1]. Numerous studies have demonstrated the accelerated precipitation of calcium carbonate minerals with the aid of carbonic anhydrase (CA) as a means of sequestering CO2 in solid carbonate form; however, no study has examined precipitation of magnesium carbonate minerals using CA. Precipitation of magnesite (MgCO3) is kinetically inhibited [2]; therefore, Mg2+ must be precipitated as hydrated carbonate minerals. In laboratory experiments, the uptake of atmospheric CO2 into brine solutions (0.1 M Mg) was rate-limiting for the precipitation of dypingite [Mg5(CO3)4(OH)2-5H2O] with initial precipitation requiring 15 days [3]. It was also found that dypingite precipitation outpaced the uptake of CO2 gas into solution. CO2 uptake is limited by the hydration of CO2 to form carbonate ions [4]. Carbonic anhydrase (CA) enzymes are among the fastest known in nature and are able to catalyze the hydration of CO2, i.e., converting CO2(aq) to CO32- and HCO3- [5]. CA plays an important role in the carbon concentrating mechanism of photoautotrophic, chemoautotrophic, and heterotrophic prokaryotes and is involved in pH homeostasis, facilitated diffusion of CO2, ion transport, and the interconversion of CO2 and HCO3- [6]. Introducing CA into buffered Mg-rich solutions should allow for more rapid precipitation of hydrated magnesium carbonate minerals. Batch experiments were conducted using 125 mL flasks containing 100 mL of Millipore deionized water with 0.2 M of MgCl2-6H2O. To buffer pH, 1.0 g of pulverized brucite [Mg(OH)2] or 1.0 g of NaOH was added to the systems, which were amended with Bovine carbonic anhydrase (BCA) (Sigma-Aldrich). Solutions were stirred continuously and kept at room temperature (~22°C) with laboratory air introduced by bubbling. Temperature and pH were measured routinely

Polymer-assisted co-precipitation route for the synthesis of Al 2 O 3

Indian Academy of Sciences (India)

It has been observed by field emission scanning electron microscopy analysis that the particle size reduced effectively (below 100 nm) when polymer-assisted co-precipitation route is used instead of the simple co-precipitation technique. A highly dense microstructure of sintered samples has been obtained, driven by ...

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

Photochemically induced deposition of protective alumina coatings onto UV emitting phosphors for Xe excimer discharge lamps

Energy Technology Data Exchange (ETDEWEB)

Broxtermann, Mike, E-mail: mike.b@fh-muenster.de; Jüstel, Thomas, E-mail: tj@fh-muenster.de

2016-08-15

Highlights: • A UV-reactor for the pH induced precipitation of inorganic material is described. • The photolysis of Azide (N{sub 3}{sup −}) leads to a steady pH increase used for precipitation. • A UV induced Al(OH){sub 3} precipitation is used to craft Al{sub 2}O{sub 3} coatings onto YPO{sub 4}:Bi. • The influence of Al{sub 2}O{sub 3} coated onto YPO{sub 4}:Bi with different thicknesses is discussed. • SEM, VUV-spectroscopy and ESA measurements were performed on Al{sub 2}O{sub 3} coated samples. - Abstract: This work concerns the particle coating of the UV-C emitting phosphor YPO{sub 4}:Bi, targeting a stability enhancement of the phosphor material for Xe excimer lamp operation. To this end, the material is coated by the wide band gap material Al{sub 2}O{sub 3}. In order to obtain a thin and homogeneous coating layer, a novel process based on the photochemical cleavage of NaN{sub 3} in water was developed. This results in a slow and continuous enhancement of the pH value due to ongoing NaOH formation, which results in the precipitation of Al(OH){sub 3} from an Al{sub 2}(SO{sub 4}){sub 3} {sub ×} 18H{sub 2}O solution. It turned out that the obtained particle coatings are of much better quality, i.e. homogeneity, compared to coatings made from a wet-chemical homogeneous precipitation process. The morphology and electrochemical properties of Al{sub 2}O{sub 3} coated YPO{sub 4}:Bi are discussed on the basis of optical spectroscopy, ESA measurements, and SEM/EDX investigations.

Novel Br-DPQ blue light-emitting phosphors for OLED.

Science.gov (United States)

Dahule, H K; Thejokalyani, N; Dhoble, S J

2015-06-01

A new series of blue light-emitting 2,4-diphenylquinoline (DPQ) substituted blue light-emitting organic phosphors namely, 2-(4-methoxy-phenyl)-4-phenyl-quinoline (OMe-DPQ), 2-(4-methyl-phenyl)-4-phenylquinoline (M-DPQ), and 2-(4-bromo-phenyl)-4-phenylquinoline (Br-DPQ) were synthesized by substituting methoxy, methyl and bromine at the 2-para position of DPQ, respectively by Friedländer condensation of 2-aminobenzophenone and corresponding acetophenone. The synthesized phosphors were characterized by different techniques, e.g., Fourier transform infra-red (FTIR), differential scanning calorimeter (DSC), UV-visible absorption and photoluminescence spectra. FTIR spectra confirms the presence of chemical groups such as C=O, NH, or OH in all the three synthesized chromophores. DSC studies show that these complexes have good thermal stability. Although they are low-molecular-weight organic compounds, they have the potential to improve the stability and operating lifetime of a device made out of these complexes. The synthesized polymeric compounds demonstrate a bright emission in the blue region in the wavelength range of 405-450 nm in solid state. Thus the attachment of methyl, methoxy and bromine substituents to the diphenyl quinoline ring in these phosphors results in colour tuning of the phosphorescence. An electroluminescence (EL) cell of Br-DPQ phosphor was made and its EL behaviour was studied. A brightness-voltage characteristics curve of Br-DPQ cell revealed that EL begins at 400 V and then the brightness increases exponentially with applied AC voltage, while current-voltage (I-V) characteristics revealed that the turn on voltage of the fabricated EL cell was 11 V. Hence this phosphor can be used as a promising blue light material for electroluminescent devices. Copyright © 2014 John Wiley & Sons, Ltd.

Chemical precipitation processes for the treatment of aqueous radioactive waste

International Nuclear Information System (INIS)

1992-01-01

Chemical precipitation by coagulation-flocculation and sedimentation has been commonly used for many years to treat liquid (aqueous) radioactive waste. This method allows the volume of waste to be substantially reduced for further treatment or conditioning and the bulk of the waste to de discharged. Chemical precipitation is usually applied in combination with other methods as part of a comprehensive waste management scheme. As with any other technology, chemical precipitation is constantly being improved to reduce cost to increase the effectiveness and safety on the entire waste management system. The purpose of this report is to review and update the information provided in Technical Reports Series No. 89, Chemical Treatment of Radioactive Wastes, published in 1968. In this report the chemical methods currently in use for the treatment of low and intermediate level aqueous radioactive wastes are described and illustrated. Comparisons are given of the advantages and limitations of the processes, and it is noted that good decontamination and volume reduction are not the only criteria according to which a particular process should be selected. Emphasis has been placed on the need to carefully characterize each waste stream, to examine fully the effect of segregation and the importance of looking at the entire operation and not just the treatment process when planning a liquid waste treatment facility. This general approach includes local requirements and possibilities, discharge authorization, management of the concentrates, ICRP recommendations and economics. It appears that chemical precipitation process and solid-liquid separation techniques will continue to be widely used in liquid radioactive waste treatment. Current research and development is showing that combining different processes in one treatment plant can provide higher decontamination factors and smaller secondary waste arisings. Some of these processes are already being incorporated into new and

Co-precipitation and solubility studies of cesium, potassium and sodium tetraphenylborate

International Nuclear Information System (INIS)

Peterson, R.A.

2000-01-01

This report contains the results from a study requested by High Level Waste on the co-precipitation and solubility of cesium, potassium, and sodium tetraphenylborate. Co-precipitation of cesium (Cs), potassium (K), and sodium (Na) tetraphenylborate (TPB) helps determine the efficiency of reagent usage in the Small Tank Precipitation Process. This process uses NaTPB to remove cesium from waste by means of precipitation. Previous studies by McCabe suggested that if the sodium ion concentration [Na + ] increased the rate at which cesium tetraphenylborate (CsTPB) precipitates also increases. Serkiz also demonstrated that the precipitation of potassium tetraphenylborate (KTPB) in the presence of high [Na + ] (∼5M) appears to produce a mixed solid phase composed of NaTPB and KTPB together in the crystal lattice. In the crystallographic structure of these three tetraphenylborate salts (Cs,K,NaTPB), the tetraphenylborate ion dominates the size of the crystals. Also, note that the three crystals have nearly identical structures with the exception of two additional peaks in the cesium pattern. Given these similarities, TPB precipitation in the presence of Na + , Cs + and K + likely produces an impure isomorphic crystalline mixture of CsTPB, KTPB and NaTPB. The authors speculate that the primary crystalline structure resembles that of KTPB with NaTPB and CsTPB mixed throughout the crystal structure. The precipitation of NaTPB makes some of the anticipated excess tetraphenylborate relatively unavailable for precipitation of cesium. Thus, the amount of excess tetraphenylborate required to completely precipitate all of the potassium and cesium may increase significantly

Synthesis and characterization of superparamagnetic nanoparticles obtained by precipitation in inverse microemulsion for biomedical applications

International Nuclear Information System (INIS)

Puca Pacheco, Mercedes; Guerrero Aquino, Marco; Tacuri Calanchi, Enrique; Lopez Campos, Raul G.

2013-01-01

In this work the preparation of nanoparticles of magnetite by methods of precipitation in inverse microemulsions and the conventional method 'Chemical Co-precipitation' is reported. Magnetite nanoparticles were characterized by X-ray diffraction, Moessbauer spectroscopy and vibrating sample magnetometer (VSM). The results showed that the nanoparticles obtained by the method of precipitation in inverse microemulsion showed a superparamagnetic behavior and had a particle average diameter of 9 nm, while by the conventional method 'Chemical Co-precipitation' were 17 nm. In addition, other benefits observed in the application of the method of precipitation in inverse microemulsion with regard to the conventional method is that it allowed obtaining spheroidal magnetite nanoparticles, monodisperse and with magnetic and chemical properties which might have better results in medical applications. (author)

Thermoluminescent dosimetry of new phosphors of Zn O exposed to beta radiation

International Nuclear Information System (INIS)

Cruz V, C.; Burruel I, S.E.; Grijalva M, H.; Barboza F, M.; Bernal, R.

2004-01-01

In this work, we report the thermoluminescence dosimetry of a new Zn O phosphor obtained by annealing of Zn S powder precipitated when Zn S films were grown by employing a CBD method. The collected Zn S powder was pressed in a die to form pellets which were subjected to different thermal treatments under air atmosphere. X-ray diffraction (XRD) patterns and energy-dispersive X-ray Spectrometry (EDS) analyses confirmed the transformation of Zn S to Zn O. The phosphors thus obtained were exposed to high doses of beta radiation and their thermoluminescent dosimetry show that these new phosphors are materials suitable to be used in high dose thermoluminescence dosimetry. (Author)

Encapsulation of strontium aluminate phosphors to enhance water resistance and luminescence

International Nuclear Information System (INIS)

Zhu Yong; Zeng Jianghua; Li Wenyu; Xu Li; Guan Qiu; Liu Yingliang

2009-01-01

Strontium aluminate SrAl 2 O 4 :Eu 2+ ,Dy 3+ phosphors are chemically unstable against water or even moisture. To enhance the water resistance of the phosphors, an encapsulation was performed by direct surface reactions with phosphoric acid (H 3 PO 4 ). The morphology, surface structure, surface element composition, water resistance, luminescence, and photoacoustic spectrum of the phosphors before and after encapsulation were discussed. Experimental results showed that phosphors were perfectly encapsulated by amorphous layers in nanoscale and crystalline layers in microscale under different conditions. The water resistance of phosphors was greatly enhanced by the two types of layer. More importantly, the amorphous layers enhanced the luminescence of phosphors markedly. The possible mechanism for the enhancements was also proposed.

Fire severity effects on ash extractable Total Phosphorous

Science.gov (United States)

Pereira, Paulo; Úbeda, Xavier; Martin, Deborah

2010-05-01

Phosphorous (P) is a crucial element to plant nutrition and limits vegetal production. The amounts of P in soil are lower and great part of this nutrient is absorbed or precipitated. It is well known that fire has important implications on P cycle, that can be lost throughout volatilization, evacuated with the smoke, but also more available to transport after organic matter mineralization imposed by the fire. The release of P depends on ash pH and their chemical and physical characteristics. Fire temperatures impose different severities, according to the specie affected and contact time. Fire severity is often evaluated by ash colour and this is a low-cost and excellent methodology to assess the fire effects on ecosystems. The aim of this work is study the ash properties physical and chemical properties on ash extractable Total Phosphorous (TP), collected in three wildfires, occured in Portugal, (named, (1) Quinta do Conde, (2) Quinta da Areia and (3) Casal do Sapo) composed mainly by Quercus suber and Pinus pinaster trees. The ash colour was assessed using the Munsell color chart. From all three plots we analyzed a total of 102 ash samples and we identified 5 different ash colours, ordered in an increasing order of severity, Very Dark Brown, Black, Dark Grey, Very Dark Grey and Light Grey. In order to observe significant differences between extractable TP and ash colours, we applied an ANOVA One Way test, and considered the differences significant at a p<0.05. The results showed that significant differences in the extractable TP among the different ash colours. Hence, to identify specific differences between each ash colour, we applied a post-hoc Fisher LSD test, significant at a p<0.05. The results obtained showed significant differences between the extractable TP from Very dark Brown and Black ash, produced at lower severities, in relation to Dark Grey, Very Dark Grey and Light Grey ash, generated at higher severities. The means of the first group were higher

Co-precipitation of plutonium(IV) and americium(III) from nitric acid-oxalic acid solutions with bismuth oxalate

International Nuclear Information System (INIS)

Pius, I.C.; Noronha, D.M.; Chaudhury, Satyajeet

2017-01-01

Co-precipitation of plutonium and americium from nitric acid-oxalic acid solutions with bismuth oxalate has been investigated for the removal of these long lived α-active nuclides from waste solutions. Effect of concentration of bismuth and oxalic acid on the co-precipitation of Pu(IV) from 3 M HNO_3 has been investigated. Similar experiments were also carried out from 3.75 M HNO_3 on co-precipitation of Am(III) to optimize the conditions of precipitation. Strong co-precipitation of Pu(IV) and Am(III) with bismuth oxalate indicate feasibility of treatment of plutonium and americium bearing waste solutions. (author)

Impact of Precipitants on the Structure and Properties of Fe-Co-Ce Composite Catalysts

Directory of Open Access Journals (Sweden)

Yongli Zhang

2016-01-01

Full Text Available Fe-Co-Ce composite catalysts were prepared by coprecipitation method using CO(NH22, NaOH, NH4HCO3, and NH3·H2O as precipitant agents. The effects of the precipitant agents on the physicochemical properties of the Fe-Co-Ce based catalysts were investigated by SEM, TEM, BET, TG-DTA, and XRD. It was found that the precipitant agents remarkably influenced the morphology and particle size of the catalysts and affected the COD removal efficiency, decolorization rate, and pH of methyl orange for catalytic wet air oxidation (CWAO. The specific surface area of the Fe-Co-Ce composite catalysts successively decreased in the order of NH3·H2O, NH4HCO3, NaOH, and CO(NH22, which correlated to an increasing particle size that increased for each catalyst. For the CWAO of a methyl orange aqueous solutions, the effects of precipitant agents NH3·H2O and NaOH were superior to those of CO(NH22 and NH4HCO3. The catalyst prepared using NH3·H2O as the precipitant agent was mostly composed of Fe2O3, CoO, and CeO2. The COD removal efficiency of methyl orange aqueous solution for NH3·H2O reached 92.9% in the catalytic wet air oxidation. Such a catalytic property was maintained for six runs.

Sequential electrodialytic recovery of phosphorus from low-temperature gasification ashes of chemically precipitated sewage sludge

DEFF Research Database (Denmark)

Parés Viader, Raimon; Jensen, Pernille Erland; Ottosen, Lisbeth M.

2017-01-01

the P solubilisation from aluminium and ferric phosphates. In addition, P was separated from most metals as they became insoluble under the prevailing chemical environment. The obtained ratio of Al, Fe, Mg and most heavy metals to P was comparable to wet process phosphoric acid. Therefore......Phosphorus recycling from secondary materials like sewage sludge ashes offers an alternative to mining of phosphates from primary resources and a mean to counteract the current phosphorous rock depletion concern. A separation of P from the bulk ash is normally required, due to its low plant......, this sequential process was found to be suitable to recycle P and potentially use it in the production of common fertilizers like diammonium phosphate. ...

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.

Influence of chemical composition of precipitation on migration of radioactive caesium in natural soils

International Nuclear Information System (INIS)

Thørring, H.; Skuterud, L.; Steinnes, E.

2014-01-01

The aim of the present work was to study the impact of the chemical composition of precipitation on radiocaesium mobility in natural soil. This was done through column studies. Three types of precipitation regimes were studied, representing a natural range found in Norway: Acidic precipitation (southernmost part of the country); precipitation rich in marine cations (highly oceanic coastal areas); and low concentrations of sea salts (slightly continental inland areas). After 50 weeks and a total precipitation supply of ∼10 000 L m −2 per column, results indicate that acidic precipitation increased the mobility of 134 Cs added during the experiment. However, depth distribution of already present Chernobyl fallout 137 Cs was not significantly affected by the chemical composition of precipitation. - Highlights: • Mobility of freshly added Cs-134 was higher in soil receiving acidic precipitation. • Depth penetration of Cs-134 was higher in soil profiles with a thicker humus layer. • Depth distribution of Chernobyl Cs-137 was not affected by precipitation type

Design of Novel Precipitate-Strengthened Al-Co-Cr-Fe-Nb-Ni High-Entropy Superalloys

Science.gov (United States)

Antonov, Stoichko; Detrois, Martin; Tin, Sammy

2018-01-01

A series of non-equiatomic Al-Co-Cr-Fe-Nb-Ni high-entropy alloys, with varying levels of Co, Nb and Fe, were investigated in an effort to obtain microstructures similar to conventional Ni-based superalloys. Elevated levels of Co were observed to significantly decrease the solvus temperature of the γ' precipitates. Both Nb and Co in excessive concentrations promoted the formation of Laves and NiAl phases that formed either during solidification and remained undissolved during homogenization or upon high-temperature aging. Lowering the content of Nb, Co, or Fe prevented the formation of the eutectic type Laves. In addition, lowering the Co content resulted in a higher number density and volume fraction of the γ' precipitates, while increasing the Fe content led to the destabilization of the γ' precipitates. Various aging treatments were performed which led to different size distributions of the strengthening phase. Results from the microstructural characterization and hardness property assessments of these high-entropy alloys were compared to a commercial, high-strength Ni-based superalloy RR1000. Potentially, precipitation-strengthened high-entropy alloys could find applications replacing Ni-based superalloys as structural materials in power generation applications.

Helix-sense-selective co-precipitation for preparing optically active helical polymer nanoparticles/graphene oxide hybrid nanocomposites.

Science.gov (United States)

Huang, Huajun; Li, Weifei; Shi, Yan; Deng, Jianping

2017-05-25

Constructing optically active helical polymer based nanomaterials without using expensive and limited chirally helical polymers has become an extremely attractive research topic in both chemical and materials science. In this study, we prepared a series of optically active helical polymer nanoparticles/graphene oxide (OAHPNs/GO) hybrid nanocomposites through an unprecedented strategy-the co-precipitation of optically inactive helical polymers and chirally modified GO. This approach is named helix-sense-selective co-precipitation (HSSCP), in which the chirally modified GO acted as a chiral source for inducing and further stabilizing the predominantly one-handed helicity in the optically inactive helical polymers. SEM and TEM images show quite similar morphologies of all the obtained OAHPNs/GO nanocomposites; specifically, the chirally modified GO sheets were uniformly decorated with spherical polymer nanoparticles. Circular dichroism (CD) and UV-vis absorption spectra confirmed the preferentially induced helicity in the helical polymers and the optical activity of the nanocomposites. The established HSSCP strategy is thus proven to be widely applicable and is expected to produce numerous functional OAHPNs/GO nanocomposites and even the analogues.

CoCoRaHS: A Community Science Program Providing Valuable Precipitation Data to Guide Decision Making

Science.gov (United States)

Robinson, D. A.; Doesken, N.

2017-12-01

CoCoRaHS is an acronym for the Community Collaborative Rain, Hail and Snow Network. It is long-running, community-based network of volunteers working together to measure and map precipitation (rain, hail and snow). Precipitation is an ideal element for public engagement because it affects everyone, it is so variable in time and space and it impacts so many things. By using a standard precipitation gauge, stressing training and education, utilizing an interactive website, and having observations undergo quality assurance, the CoCoRaHS program provides high-quality data for natural resource, education and research applications. The program currently operates in all states, Canada and the Bahamas. It originated with the Colorado Climate Center at Colorado State University in 1998 due in part to the Fort Collins flood a year prior. Upwards of 12,000 observers submit observations each day. Observations meet federal guidelines and are archived at the U.S. National Centers for Environmental Information. Because of excellent spatial coverage, data quality, practical relevance, and accessibility, CoCoRaHS observations are used by a wide variety of organizations and individuals. The U.S. National Weather Service, hydrologists, emergency managers, city utilities (water supply, storm water), insurance adjusters, the U.S. Department of Agriculture, engineers, mosquito control commissions, ranchers and farmers, outdoor and recreation interests, teachers and students are just some examples of those who use CoCoRaHS data in making well-informed, meaningful decisions. Some examples of community applications and the science utility of CoCoRaHS observations include storm warnings, water supply and demand forecasts, disaster declarations (drought, winter storm, etc.), drought and food production assessments, calibration/validation of remote sensing, infrastructure evaluation and potential redesign (ice and snow loading, bridge, storm and sewer design), recreation planning, and

Synthesis of YAG nanopowder by the co-precipitation method: Influence of pH and study of the reaction mechanisms

Science.gov (United States)

Marlot, Caroline; Barraud, Elodie; Le Gallet, Sophie; Eichhorn, Marc; Bernard, Frédéric

2012-07-01

YAG nanopowders with an average grain size of 30 nm have been successfully synthesized by the co-precipitation method using nitrates with precipitant of ammonium hydrogen carbonate. The influence of precipitation conditions such as pH, aging time and calcination temperature on the formation of secondary phases has been studied. The accurate control of pH value at every stage of precipitation process is crucial to avoid the presence of YAM (Yttrium Aluminium Monoclinic, Y4Al2O9) and yttrium oxide (Y2O3) after calcination. The reaction mechanisms have been investigated using different techniques such as infrared spectroscopy, x-ray diffraction and thermal analyses. The YAG phase is formed around 1050 °C passing through an intermediate phase called YAP (Yttrium Aluminium Perovskite, YAlO3). Local chemical heterogeneities are responsible for the deviation of the Y:Al ratio and the formation of YAP during heat treatment.

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.

Pyrolysis synthesis of Zn{sub 2}SiO{sub 4}:Mn{sup 2+} phosphors – effect of fuel, flux and co-dopants

Energy Technology Data Exchange (ETDEWEB)

Sivakumar, V.; Lakshmanan, Arunachalam, E-mail: arunachalamlakshmanan@yahoo.com

2014-01-15

Green emitting α-Zn{sub 2}SiO{sub 4}:Mn{sup 2+} phosphors were made by pyrolysis route at 600 °C followed by sintering at a moderate temperature of 1000 °C for 1 h duration. The effects of different fuels (urea, citric acid, polyethylene glycol and glycine), flux materials (H{sub 3}BO{sub 3}, NH{sub 4}Cl, NH{sub 4}F, NH{sub 4}Br, BaCl{sub 2}, BaBr{sub 2}, CaF{sub 2} and BaF{sub 2}), divalant co-dopants (Ca{sup 2+}, Ba{sup 2+}, Mg{sup 2+} and Sr{sup 2+}), trivalent co-dopants (Al{sup 3+}, Y{sup 3+} and Gd{sup 3+}) and sintering temperature (800–1000 °C) on the photoluminescence (PL) efficiency of Zn{sub 2}SiO{sub 4}:Mn{sup 2+} were studied. Among the fuels, urea and among the flux, H{sub 3}BO{sub 3} gave a maximum broad band green PL emission peak at 525 nm on excitation at 254 nm. Divalent co-dopants improved the PL intensity much more than the trivalent co-dopants used. Highest PL efficiency was observed with Sr{sup 2+} co-doped Zn{sub 2}SiO{sub 4}:Mn{sup 2+} sintered at 1000 °C in reducing atmosphere which was 20% higher than that of the commercial Zn{sub 2}SiO{sub 4}:Mn{sup 2+}. The formation of a single crystalline phase of willemite structure in the α-Zn{sub 2}SiO{sub 4}:Mn{sup 2+} samples synthesized was confirmed by powder XRD measurements. -- Highlights: • Zn{sub 2}SiO{sub 4}:Mn{sup 2+} green phosphors were made by pyrolysis route. • Effect of fuel, flux and co dopant on PL intensity. • Enhancement in luminescence with divalent co-dopants, notably Sr. • PL efficiency 20% higher than that of the commercial phosphor. • XRD confirm single phase willemite structure of Zn{sub 2}SiO{sub 4}:Mn{sup 2+}.

Room Temperature Gas Sensing Properties of Sn-Substituted Nickel Ferrite (NiFe2O4) Thin Film Sensors Prepared by Chemical Co-Precipitation Method

Science.gov (United States)

Manikandan, V.; Li, Xiaogan; Mane, R. S.; Chandrasekaran, J.

2018-04-01

Tin (Sn) substituted nickel ferrite (NiFe2O4) thin film sensors were prepared by a simple chemical co-precipitation method, which initially characterized their structure and surface morphology with the help of x-ray diffraction and scanning electron microscopy. Surface morphology of the sensing films reveals particles stick together with nearer particles and this formation leads to a large specific area as a large specific area is very useful for easy adsorption of gas molecules. Transmission electron microscopy and selected area electron diffraction pattern images confirm particle size and nanocrystallnity as due to formation of circular rings. Fourier transform infrared analysis has supported the presence of functional groups. The 3.69 eV optical band gap of the film was found which enabled better gas sensing. Gas sensors demonstrate better response and recovery characteristics, and the maximum response was 68.43%.

Oxycarbonitride phosphors and light emitting devices using the same

Science.gov (United States)

Li, Yuanqiang; Romanelli, Michael Dennis; Tian, Yongchi

2013-10-08

Disclosed herein is a novel family of oxycarbidonitride phosphor compositions and light emitting devices incorporating the same. Within the sextant system of M--Al--Si--O--N--C--Ln and quintuplet system of M--Si--O--N--C--Ln (M=alkaline earth element, Ln=rare earth element), the phosphors are composed of either one single crystalline phase or two crystalline phases with high chemical and thermal stability. In certain embodiments, the disclosed phosphor of silicon oxycarbidonitrides emits green light at wavelength between 530-550 nm. In further embodiments, the disclosed phosphor compositions emit blue-green to yellow light in a wavelength range of 450-650 nm under near-UV and blue light excitation.

Novel tunable green-red-emitting oxynitride phosphors co-activated with Ce3+, Tb3+, and Eu3+: photoluminescence and energy transfer.

Science.gov (United States)

Huo, Jiansheng; Dong, Langping; Lü, Wei; Shao, Baiqi; You, Hongpeng

2017-07-14

A series of novel Ce 3+ , Tb 3+ and Eu 3+ ion doped Y 4 SiAlO 8 N-based oxynitride phosphors were synthesized by the solid-state method and characterized by X-ray powder diffraction, scanning electron microscopy, photoluminescence, lifetimes and thermo-luminescence. The excitation of the Ce 3+ /Tb 3+ co-doped and Ce 3+ /Tb 3+ /Eu 3+ tri-doped phosphor with near-UV radiation results in strong linear Tb 3+ green and Eu 3+ red emission. The occurrence of Ce 3+ -Tb 3+ and Ce 3+ -Tb 3+ -Eu 3+ energy transfer processes is responsible for the bright green or red luminescence. The Tb 3+ ion acting as an energy transfer bridge can alleviate MMCT quenching between the Ce 3+ -Eu 3+ ion pairs. The lifetime measurements demonstrated that the energy-transfer mechanisms of Ce 3+ → Tb 3+ and Tb 3+ → Eu 3+ are dipole-quadrupole and quadrupole-quadrupole interactions, respectively. The temperature dependent luminescence measurements showed that as-prepared green/red phosphors have good thermal stability against temperature quenching. The obtained results indicate that these phosphors might serve as promising candidates for n-UV LEDs.

Development of Hydrotalcite Based Cobalt Catalyst by Hydrothermal and Co-precipitation Method for Fischer-Tropsch Synthesis

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Muhammad Faizan Shareef

2017-10-01

Full Text Available This paper presents the effect of a synthesis method for cobalt catalyst supported on hydrotalcite material for Fischer-Tropsch synthesis. The hydrotalcite supported cobalt (HT-Co catalysts were synthesized by co-precipitation and hydrothermal method. The prepared catalysts were characterized by using various techniques like BET (Brunauer–Emmett–Teller, SEM (Scanning Electron Microscopy, TGA (Thermal Gravimetric Analysis, XRD (X-ray diffraction spectroscopy, and FTIR (Fourier Transform Infrared Spectroscopy. Fixed bed micro reactor was used to test the catalytic activity of prepared catalysts. The catalytic testing results demonstrated the performance of hydrotalcite based cobalt catalyst in Fischer-Tropsch synthesis with high selectivity for liquid products. The effect of synthesis method on the activity and selectivity of catalyst was also discussed. Copyright © 2017 BCREC Group. All rights reserved Received: 3rd November 2016; Revised: 26th February 2017; Accepted: 9th March 2017; Available online: 27th October 2017; Published regularly: December 2017 How to Cite: Sharif, M.S., Arslan, M., Iqbal, N., Ahmad, N., Noor, T. (2017. Development of Hydrotalcite Based Cobalt Catalyst by Hydrothermal and Co-precipitation Method for Fischer-Tropsch Synthesis. Bulletin of Chemical Reaction Engineering & Catalysis, 12(3: 357-363 (doi:10.9767/bcrec.12.3.762.357-363

Sensitive indicators of Stipa bungeana response to precipitation under ambient and elevated CO2 concentration

Science.gov (United States)

Shi, Yaohui; Zhou, Guangsheng; Jiang, Yanling; Wang, Hui; Xu, Zhenzhu

2018-02-01

Precipitation is a primary environmental factor in the semiarid grasslands of northern China. With increased concentrations of atmospheric greenhouse gases, precipitation regimes will change, and high-impact weather events may be more common. Currently, many ecophysiological indicators are known to reflect drought conditions, but these indicators vary greatly among species, and few studies focus on the applicability of these drought indicators under high CO2 conditions. In this study, five precipitation levels (- 30%, - 15%, control, + 15%, and + 30%) were used to simulate the effects of precipitation change on 18 ecophysiological characteristics in Stipa bungeana, including leaf area, plant height, leaf nitrogen (N), and chlorophyll content, among others. Two levels of CO2 concentration (ambient, 390 ppm; 550 ppm) were used to simulate the effects of elevated CO2 on these drought indicators. Using gray relational analysis and phenotypic plasticity analysis, we found that total leaf area or leaf number (morphology), leaf water potential or leaf water content (physiology), and aboveground biomass better reflected the water status of S. bungeana under ambient and elevated CO2 than the 13 other analyzed variables. The sensitivity of drought indicators changed under the elevated CO2 condition. By quantifying the relationship between precipitation and the five most sensitive indicators, we found that the thresholds of precipitation decreased under elevated CO2 concentration. These results will be useful for objective monitoring and assessment of the occurrence and development of drought events in S. bungeana grasslands.

Production of mixed oxide fuel for fast reactor irradiation test by co-precipitation

International Nuclear Information System (INIS)

Todokoro, Akio; Masuda, Sumio; Naruki, Kaoru; Kaya, Akira; Koizumi, Masumichi

1974-01-01

Studies were made on the production of homogeneous mixed oxide by co-precipitation. Experiments were made on the effects of the addition rate of ammonia water, precipitation temperature, aging time of co-precipitate, and pH value. Plutonium refined by anion exchange was mixed with solution of uranium. The concentration of free acid in the mixed solution was adjusted to 1.5-2.0 M, and the total volume of the solution was made 3.01. The weight of Pu and U in the solution was 100g. The solution was kept at a definite temperature while being stirred. Concentrated ammonia solution was added to the solution at a definite rate. The precipitate thus formed was filtrated after aging, then dried for 24 hours at 100 +- 2 0 C. Dried co-precipitate was calcinated for 1 hr at 550 0 C. The reduction for 4 hours at 800 0 C gave the mixed powder of PuO 2 and UO 2 . After pressing, the powder was sintered for 2 hours at 1700 0 C. The shrinkage ratio decreased as the activity and tap density of the original powder increased. The activity determined by specific surface area increased as the rate of ammonia water addition increased, and as the precipitation temperature rose. Tap density was independent of the rate of addition of ammonia water. The activity of the powder increased and the tap density decreased as the aging time of precipitate increased. (Fukutomi, T.)

Synthesis and optical properties of red/blue-emitting Sr2MgSi2O7:Eu3+/Eu2+ phosphors for white LED

Directory of Open Access Journals (Sweden)

Tong Thi Hao Tam

2016-06-01

Full Text Available Phosphor-converted white light emitting diodes (white LEDs have received great attention in recent years since they have several excellent features such as high lumen output, low power consumption, long lifetime and environmentally friendly. In this work, we report the co-precipitation synthesis of red/blue Sr2MgSi2O7:Eu3+/Eu2+ phosphors with various Eu doping concentration. The results show that the obtained Sr2MgSi2O7:Eu3+/Eu2+ phosphors have good crystallinity and emit strong red (Sr2MgSi2O7:Eu3+ and blue (Sr2MgSi2O7:Eu2+ emissions under near UV light excitation. The sharp emission peaks at 577, 590, 612, 653, and 701 nm corresponded to the typical 5D0 → 7Fj (j = 0,1,2,3,4 transitions of Eu3+, and the blue emission peaking at 460 nm is attributed to the typical 4f65d1-4f7 transition of Eu2+ in the same Sr2MgSi2O7 host lattice. Both phosphors can be well excited in the wavelength range of 260–400 nm where the near UV-LED is well matched. The above results suggest that the Sr2MgSi2O7:Eu3+/Eu2+ phosphors are promising red/blue-emitting phosphors for the application in near UV pumped phosphor-converted white LEDs.

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.

Self-aligned nanocrystalline ZnO hexagons by facile solid-state and co-precipitation route

International Nuclear Information System (INIS)

Thorat, J. H.; Kanade, K. G.; Nikam, L. K.; Chaudhari, P. D.; Panmand, R. P.; Kale, B. B.

2012-01-01

In this study, we report the synthesis of well-aligned nanocrystalline hexagonal zinc oxide (ZnO) nanoparticles by facile solid-state and co-precipitation method. The co-precipitation reactions were performed using aqueous and ethylene glycol (EG) medium using zinc acetate and adipic acid to obtain zinc adipate and further decomposition at 450 °C to confer nanocrystalline ZnO hexagons. XRD shows the hexagonal wurtzite structure of the ZnO. Thermal study reveals complete formation of ZnO at 430 °C in case of solid-state method, whereas in case of co-precipitation method complete formation was observed at 400 °C. Field emission scanning electron microscope shows spherical morphology for ZnO synthesized by solid-state method. The aqueous-mediated ZnO by co-precipitation method shows rod-like morphology. These rods are formed via self assembling of spherical nanoparticles, however, uniformly dispersed spherical crystallites were seen in EG-mediated ZnO. Transmission electron microscope (TEM) investigations clearly show well aligned and highly crystalline transparent and thin hexagonal ZnO. The particle size was measured using TEM and was observed to be 50–60 nm in case of solid-state method and aqueous-mediated co-precipitation method, while 25–50 nm in case of EG-mediated co-precipitation method. UV absorption spectra showed sharp absorption peaks with a blue shift for EG-mediated ZnO, which demonstrate the mono-dispersed lower particle size. The band gap of the ZnO was observed to be 3.4 eV which is higher than the bulk, implies nanocrystalline nature of the ZnO. The photoluminescence studies clearly indicate the strong violet and weak blue emission in ZnO nanoparticles which is quite unique. The process investigated may be useful to synthesize other oxide semiconductors and transition metal oxides.

Self-aligned nanocrystalline ZnO hexagons by facile solid-state and co-precipitation route

Energy Technology Data Exchange (ETDEWEB)

Thorat, J. H. [Mahatma Phule College, Department of Chemistry (India); Kanade, K. G. [Annasaheb Awate College (India); Nikam, L. K. [B.G. College (India); Chaudhari, P. D.; Panmand, R. P.; Kale, B. B., E-mail: kbbb1@yahoo.com [Center for Materials for Electronics Technology (C-MET) (India)

2012-02-15

In this study, we report the synthesis of well-aligned nanocrystalline hexagonal zinc oxide (ZnO) nanoparticles by facile solid-state and co-precipitation method. The co-precipitation reactions were performed using aqueous and ethylene glycol (EG) medium using zinc acetate and adipic acid to obtain zinc adipate and further decomposition at 450 Degree-Sign C to confer nanocrystalline ZnO hexagons. XRD shows the hexagonal wurtzite structure of the ZnO. Thermal study reveals complete formation of ZnO at 430 Degree-Sign C in case of solid-state method, whereas in case of co-precipitation method complete formation was observed at 400 Degree-Sign C. Field emission scanning electron microscope shows spherical morphology for ZnO synthesized by solid-state method. The aqueous-mediated ZnO by co-precipitation method shows rod-like morphology. These rods are formed via self assembling of spherical nanoparticles, however, uniformly dispersed spherical crystallites were seen in EG-mediated ZnO. Transmission electron microscope (TEM) investigations clearly show well aligned and highly crystalline transparent and thin hexagonal ZnO. The particle size was measured using TEM and was observed to be 50-60 nm in case of solid-state method and aqueous-mediated co-precipitation method, while 25-50 nm in case of EG-mediated co-precipitation method. UV absorption spectra showed sharp absorption peaks with a blue shift for EG-mediated ZnO, which demonstrate the mono-dispersed lower particle size. The band gap of the ZnO was observed to be 3.4 eV which is higher than the bulk, implies nanocrystalline nature of the ZnO. The photoluminescence studies clearly indicate the strong violet and weak blue emission in ZnO nanoparticles which is quite unique. The process investigated may be useful to synthesize other oxide semiconductors and transition metal oxides.

Thermally and optically stimulated luminescence of new ZnO nano phosphors exposed to beta radiation

International Nuclear Information System (INIS)

Cruz V, C.; Burruel I, S.E.; Grijalva M, H.; Chernov, V.; Bernal, R.

2006-01-01

In this work, we report the thermoluminescence (TL) and the optically stimulated luminescence (OSL) of ZnO nano phosphors obtained by thermal annealing of ZnS powders synthesized by precipitation in a chemical bath deposition reaction. To obtain nanocrystalline ZnO, ZnS pellet-shaped samples were subjected to a sintering process at 700 C during 24 under air atmosphere. Some samples were exposed to beta particles in the 0.15-10.15 kGy dose range and the integrated thermoluminescence as a function of dose increased as dose increased, with no saturation clue for the tested doses. Computerized glow-curve deconvolution of the experimental TL curves in individual peaks revealed a second order kinetics. In order to test the BOSL (Blue Optically Stimulated Luminescence) response, samples were beta irradiated with doses up to 600 Gy, showing an increasing OSL intensity as dose increases. From the experimental results that we have obtained, we conclude that the new ZnO phosphors under investigation are good candidates to be used as dosimetric materials. (Author)

Magnetic Field Effects on CaCO3 Precipitation Process in Hard Water

Directory of Open Access Journals (Sweden)

Nelson Saksono

2010-10-01

Full Text Available Magnetic treatment is applied as physical water treatment for scale prevention especially CaCO3, from hard water in piping equipment by reducing its hardness.Na2CO3 and CaCl2 solution sample was used in to investigate the magnetic fields influence on the formation of particle of CaCO3. By changing the strength of magnetic fields, exposure time and concentration of samples solution, this study presents quantitative results of total scale deposit, total precipitated CaCO3 and morphology of the deposit. This research was run by comparing magnetically and non-magnetically treated  samples. The results showed an increase of deposits formation rate and total number of precipitated CaCO3 of magnetically treated samples. The increase of concentration solution sample will also raised the deposit under magnetic  field. Microscope images showed a greater number but smaller size of CaCO3 deposits form in magnetically treated samples, and aggregation during the processes. X-ray diffraction (XRD analysis showed that magnetically samples were dominated by calcite. But, there was a significant decrease of calcite’s peak intensities from magnetized  samples that indicated the decrease of the amount of calcite and an increase of total amorphous of deposits. This result  showed that magnetization of hard water leaded to the decreasing of ion Ca2+ due to the increasing of total CaCO3 precipitation process.

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.

Chemical composition of precipitation in adjacent forest and open plots

Energy Technology Data Exchange (ETDEWEB)

Madgwick, H A.I.; Ovington, J D

1959-01-01

The chemical composition of the precipitation in three open plots and under thirteen different forest canopies is compared for a 2-year period at an experimental forest in south-east England. The average contents of sodium, potassium, calcium, and magnesium in the precipitation in the open are 19, 3, 11, and less than 4 kg./ha./annum respectively, compared with 33, 24, 24, and 10 under the forest canopies. Only very small quantities of phosphorus were present in the precipitation. The data are discussed with particular reference to the nutrient cycles of forest stands, the removal of nutrients by logging, and the maintenance of soil fertility.

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

Kinetic study of the precipitation of radioactive elements in the production process of phosphoric acid

International Nuclear Information System (INIS)

Ben Mahmoud, Souha

2009-01-01

In this engineering study we determined the activities of gamma emitting radionuclides belonging to the families of 238 U , 232 Th and 40K in phosphate, the acid derivatives and gypsum in Tunisian Chemical Group. The most important activities are those of 238 U and 226 Ra, which are located in the phosphate, gypsum and the precipitates formed in the pipes.

Structural variation study of cobalt nanoparticles synthesized by co-precipitation method using 59Co NMR

Science.gov (United States)

Manjunatha, M.; Kumar, Rajeev; B. M., Siddesh; Sahoo, Balaram; Damle, R.; Ramesh, K. P.

2018-04-01

We have synthesized cobalt nanoparticles using co-precipitation method. Further, the two phases of the cobalt is monitored by varying the synthesis parameters. 59Co NMR and XRD are used as characterization tools to study the phase variation in the cobalt samples. XRD and NMR results show a remarkable correlation in the two samples (Co-1 and Co-2). Co-2 has predominant fcc and hcp phases, whereas, Co-1 has fcc phase with lower amount of hcp. Both the samples show same saturation magnetization (Ms) but there is a remarkable difference in the phase composition. Thus, 59Co NMR appears to be a good tool to identify the phase purity of the ferromagnetic cobalt samples.

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

All-in-one light-tunable borated phosphors with chemical and luminescence dynamical control resolution.

Science.gov (United States)

Lin, Chun Che; Liu, Yun-Ping; Xiao, Zhi Ren; Wang, Yin-Kuo; Cheng, Bing-Ming; Liu, Ru-Shi

2014-06-25

Single-composition white-emitting phosphors with superior intrinsic properties upon excitation by ultraviolet light-emitting diodes are important constituents of next-generation light sources. Borate-based phosphors, such as NaSrBO3:Ce(3+) and NaCaBO3:Ce(3+), have stronger absorptions in the near-ultraviolet region as well as better chemical/physical stability than oxides. Energy transfer effects from sensitizer to activator caused by rare-earth ions are mainly found in the obtained photoluminescence spectra and lifetime. The interactive mechanisms of multiple dopants are ambiguous in most cases. We adjust the doping concentration in NaSrBO3:RE (RE = Ce(3+), Tb(3+), Mn(2+)) to study the energy transfer effects of Ce(3+) to Tb(3+) and Mn(2+) by comparing the experimental data and theoretical calculation. The vacuum-ultraviolet experimental determination of the electronic energy levels for Ce(3+) and Tb(3+) in the borate host regarding the 4f-5d and 4f-4f configurations are described. Evaluation of the Ce(3+)/Mn(2+) intensity ratios as a function of Mn(2+) concentration is based on the analysis of the luminescence dynamical process and fluorescence lifetime measurements. The results closely agree with those directly obtained from the emission spectra. Density functional calculations are performed using the generalized gradient approximation plus an on-site Coulombic interaction correction scheme to investigate the forbidden mechanism of interatomic energy transfer between the NaSrBO3:Ce(3+) and NaSrBO3:Eu(2+) systems. Results indicate that the NaSrBO3:Ce(3+), Tb(3+), and Mn(2+) phosphors can be used as a novel white-emitting component of UV radiation-excited devices.

Nanoscale Chemical Processes Affecting Storage Capacities and Seals during Geologic CO2 Sequestration.

Science.gov (United States)

Jun, Young-Shin; Zhang, Lijie; Min, Yujia; Li, Qingyun

2017-07-18

Geologic CO 2 sequestration (GCS) is a promising strategy to mitigate anthropogenic CO 2 emission to the atmosphere. Suitable geologic storage sites should have a porous reservoir rock zone where injected CO 2 can displace brine and be stored in pores, and an impermeable zone on top of reservoir rocks to hinder upward movement of buoyant CO 2 . The injection wells (steel casings encased in concrete) pass through these geologic zones and lead CO 2 to the desired zones. In subsurface environments, CO 2 is reactive as both a supercritical (sc) phase and aqueous (aq) species. Its nanoscale chemical reactions with geomedia and wellbores are closely related to the safety and efficiency of CO 2 storage. For example, the injection pressure is determined by the wettability and permeability of geomedia, which can be sensitive to nanoscale mineral-fluid interactions; the sealing safety of the injection sites is affected by the opening and closing of fractures in caprocks and the alteration of wellbore integrity caused by nanoscale chemical reactions; and the time scale for CO 2 mineralization is also largely dependent on the chemical reactivities of the reservoir rocks. Therefore, nanoscale chemical processes can influence the hydrogeological and mechanical properties of geomedia, such as their wettability, permeability, mechanical strength, and fracturing. This Account reviews our group's work on nanoscale chemical reactions and their qualitative impacts on seal integrity and storage capacity at GCS sites from four points of view. First, studies on dissolution of feldspar, an important reservoir rock constituent, and subsequent secondary mineral precipitation are discussed, focusing on the effects of feldspar crystallography, cations, and sulfate anions. Second, interfacial reactions between caprock and brine are introduced using model clay minerals, with focuses on the effects of water chemistries (salinity and organic ligands) and water content on mineral dissolution and

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.

Procedure to use phosphogypsum industrial waste for mineral CO{sub 2} sequestration

Energy Technology Data Exchange (ETDEWEB)

Cardenas-Escudero, C. [Departamento de Fisica de la Materia Condensada, Facultad de Fisica, Universidad de Sevilla, Av. Reina Mercedes s/n, 41012 Seville (Spain); Instituto de Ciencia de Materiales de Sevilla (CSIC-US), Av. Americo Vespucio, 49, 41092 Seville (Spain); Morales-Florez, V., E-mail: victor.morales@icmse.csic.es [Instituto de Ciencia de Materiales de Sevilla (CSIC-US), Av. Americo Vespucio, 49, 41092 Seville (Spain); Perez-Lopez, R. [Departamento de Geologia, Facultad de Ciencias Experimentales, Universidad de Huelva, Campus Universitario Campus del Carmen, Avenida de las Fuerzas Armadas, 21071 Huelva (Spain); Instituto de Diagnostico Ambiental y Estudios del Agua (IDAeA-CSIC), Jordi Girona 18, 08034 Barcelona (Spain); Santos, A. [Departamento de Ciencias de la Tierra, Universidad de Cadiz, Campus del Rio San Pedro, Av. Republica Saharaui s/n, 11510 Puerto Real (Spain); Esquivias, L. [Departamento de Fisica de la Materia Condensada, Facultad de Fisica, Universidad de Sevilla, Av. Reina Mercedes s/n, 41012 Seville (Spain); Instituto de Ciencia de Materiales de Sevilla (CSIC-US), Av. Americo Vespucio, 49, 41092 Seville (Spain)

2011-11-30

Highlights: Black-Right-Pointing-Pointer Phosphogypsum wastes are proposed to reduce CO{sub 2} greenhouse gas emissions. Black-Right-Pointing-Pointer Phosphogypsum dissolution with NaOH results in Ca(OH){sub 2} precipitation and Na{sub 2}SO{sub 4}. Black-Right-Pointing-Pointer Aqueous carbonation of Ca(OH){sub 2} with CO{sub 2} results in the CaCO{sub 3} precipitation. Black-Right-Pointing-Pointer Metals contained in the phosphogypsum are transferred to the final calcite. Black-Right-Pointing-Pointer Applications of CaCO{sub 3} and Na{sub 2}SiO{sub 4} by-products are proposed to improve viability. - Abstract: Industrial wet phosphoric acid production in Huelva (SW Spain) has led to the controversial stockpiling of waste phosphogypsum by-products, resulting in the release of significant quantities of toxic impurities in salt marshes in the Tinto river estuary. In the framework of the fight against global climate change and the effort to reduce carbon dioxide emissions, a simple and efficient procedure for CO{sub 2} mineral sequestration is presented in this work, using phosphogypsum waste as a calcium source. Our results demonstrate the high efficiency of portlandite precipitation by phosphogypsum dissolution using an alkaline soda solution. Carbonation experiments performed at ambient pressure and temperature resulted in total conversion of the portlandite into carbonate. The fate of trace elements present in the phosphogypsum waste was also investigated, and trace impurities were found to be completely transferred to the final calcite. We believe that the procedure proposed here should be considered not only as a solution for reducing old stockpiles of phosphogypsum wastes, but also for future phosphoric acid and other gypsum-producing industrial processes, resulting in more sustainable production.

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)

1997 toxic chemical release inventory. Emergency Planning and Community Right-To-Know Act, Section 313

International Nuclear Information System (INIS)

Zaloudek, D.E.

1998-01-01

Two listed toxic chemicals were used at the Hanford Site above established activity thresholds: phosphoric acid and chlorine. Because total combined quantities of chlorine released, disposed, treated, recovered through recycle operations, co-combusted for energy recovery, and transferred to off-site locations for the purpose of recycle, energy recovery, treatment, and/or disposal, amounted to less than 500 pounds, the Hanford Site qualified for the alternate one million pound threshold for chlorine. Accordingly, this Toxic Chemical Release Inventory includes a Form A for chlorine, and a Form B for phosphoric acid

Synthesis and characterization of M-type barium hexferrite by ultrasonic inter-dispersion of chemical precipitate

International Nuclear Information System (INIS)

Garcia Junior, E.S.; Gomes Junior, G.G.; Ogasawara, T.

2010-01-01

This work is concerned with the study the synthesis and characterization of M-type barium hexaferrite powder by chemical precipitation type and ultrasonic interdispersion of precursor materials Fe(OH) 3 and Ba(OH) 2 ,separately and ultrasonic inter-dispersion, followed by drying and calcining. In order to guide the experimental work was carried out a preliminary thermodynamic analysis of the system Ba-Fe-H 2 O at 25 deg C. The study shows that the phase formation of M-type barium hexaferrite is obtained at a calcination at 1000 deg C, characterized by X-ray diffraction, the grain growth of the final product of synthesis depending on the calcination temperature is visible by SEM. The synthesis method developed in this research is an option to achieve the results that would be obtained if the co-precipitation of ferric and barium hydroxide was thermodynamically possible, where you can get crystallization of barium hexaferrite in a calcination at 1000 deg C. (author)

Influence of Chemical, Mechanical, and Transport Processes on Wellbore Leakage from Geologic CO2 Storage Reservoirs.

Science.gov (United States)

Carroll, Susan A; Iyer, Jaisree; Walsh, Stuart D C

2017-08-15

Wells are considered to be high-risk pathways for fluid leakage from geologic CO 2 storage reservoirs, because breaches in this engineered system have the potential to connect the reservoir to groundwater resources and the atmosphere. Given these concerns, a few studies have assessed leakage risk by evaluating regulatory records, often self-reported, documenting leakage in gas fields. Leakage is thought to be governed largely by initial well-construction quality and the method of well abandonment. The geologic carbon storage community has raised further concerns because acidic fluids in the CO 2 storage reservoir, alkaline cement meant to isolate the reservoir fluids from the overlying strata, and steel casings in wells are inherently reactive systems. This is of particular concern for storage of CO 2 in depleted oil and gas reservoirs with numerous legacy wells engineered to variable standards. Research suggests that leakage risks are not as great as initially perceived because chemical and mechanical alteration of cement has the capacity to seal damaged zones. Our work centers on defining the coupled chemical and mechanical processes governing flow in damaged zones in wells. We have developed process-based models, constrained by experiments, to better understand and forecast leakage risk. Leakage pathways can be sealed by precipitation of carbonate minerals in the fractures and deformation of the reacted cement. High reactivity of cement hydroxides releases excess calcium that can precipitate as carbonate solids in the fracture network under low brine flow rates. If the flow is fast, then the brine remains undersaturated with respect to the solubility of calcium carbonate minerals, and zones depleted in calcium hydroxides, enriched in calcium carbonate precipitates, and made of amorphous silicates leached of original cement minerals are formed. Under confining pressure, the reacted cement is compressed, which reduces permeability and lowers leakage risks. The

The use of simultaneous chemical precipitation in modified activated ...

African Journals Online (AJOL)

The IAWQ Activated Sludge Model (ASM) No. 2 is a kinetic-based model and incorporates two simple processes for chemical precipitation and redissolution that are readily integrated with biological processes for carbon, nitrogen and phosphorus removal. This model was applied to experimental data collected as part of this ...

A study of the fixing of phosphoric ions by zirconium-montmorillonite; Etude de la fixation d'ions phosphoriques par la montmorillonite-zirconium

Energy Technology Data Exchange (ETDEWEB)

Bittel, R; Boursat, C; Platzer, R [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

1960-07-01

In connection with the research carried out on the purification of nuclear reactor water, we have undertaken a study of the ion-exchange properties of acid montmorillonite. In a previous paper, we described the preparation of zirconium-montmorillonite small plate. The present article aims to study some of the properties of the clay obtained. We have observed that zirconium-montmorillonite fixes very strongly the phosphorus from solutions of phosphoric acid or of phosphates: on 1 g of clay it is possible to fix 1,2 milli-atoms-gram of zirconium and the zirconium montmorillonite itself fixes 2,1 milli-atoms-gram of phosphorus. An explanation of these experimental results, which is as much chemical as mineralogical, is the hypothesis that the fixing of phosphoric ions modifies the distribution of the ions between the platelets and precipitates a very slightly soluble product of the type diphospho-zirconic acid. (author) [French] En rapport avec des recherches sur I'epuration de l'eau des reacteurs nucleaires nous avons entrepris une etude sur les proprietes d'echangeur d'ions de la montmorillonite-acide. Dans une precedente publication, nous avons decrit la preparation des plaquettes de montmorillonite-zirconium. La presente communication a pour but d'etudier quelques proprietes de l'argile obtenue. Nous avons constate que la montmorilionite-zirconium fixe le phosphore de solutions d'acide phosphorique ou de phosphate avec une grande intensite: sur 1 g d'argile, on peut fixer 1,2 atomes-gramme de zirconium, et la montmorillonite-zirconium fixe a son tour 2,1 milli-atomesgramme de phosphore. Une explication des resultats experimentaux, tant d'ordre chimique que d'ordre mineralogique, consiste en l'hypothese suivant laquelle la fixation d'ions phosphoriques modifierait la repartition des ions entre les feuillets avec precipitation du compose tres peu soluble (type: acide diphosphozirconique). (auteur)

Effect of Mineral Dissolution/Precipitation and CO2 Exsolution on CO2 transport in Geological Carbon Storage.

Science.gov (United States)

Xu, Ruina; Li, Rong; Ma, Jin; He, Di; Jiang, Peixue

2017-09-19

Geological carbon sequestration (GCS) in deep saline aquifers is an effective means for storing carbon dioxide to address global climate change. As the time after injection increases, the safety of storage increases as the CO 2 transforms from a separate phase to CO 2 (aq) and HCO 3 - by dissolution and then to carbonates by mineral dissolution. However, subsequent depressurization could lead to dissolved CO 2 (aq) escaping from the formation water and creating a new separate phase which may reduce the GCS system safety. The mineral dissolution and the CO 2 exsolution and mineral precipitation during depressurization change the morphology, porosity, and permeability of the porous rock medium, which then affects the two-phase flow of the CO 2 and formation water. A better understanding of these effects on the CO 2 -water two-phase flow will improve predictions of the long-term CO 2 storage reliability, especially the impact of depressurization on the long-term stability. In this Account, we summarize our recent work on the effect of CO 2 exsolution and mineral dissolution/precipitation on CO 2 transport in GCS reservoirs. We place emphasis on understanding the behavior and transformation of the carbon components in the reservoir, including CO 2 (sc/g), CO 2 (aq), HCO 3 - , and carbonate minerals (calcite and dolomite), highlight their transport and mobility by coupled geochemical and two-phase flow processes, and consider the implications of these transport mechanisms on estimates of the long-term safety of GCS. We describe experimental and numerical pore- and core-scale methods used in our lab in conjunction with industrial and international partners to investigate these effects. Experimental results show how mineral dissolution affects permeability, capillary pressure, and relative permeability, which are important phenomena affecting the input parameters for reservoir flow modeling. The porosity and the absolute permeability increase when CO 2 dissolved water is

and aluminum-substituted cobalt ferrite prepared by co-precipitation

Indian Academy of Sciences (India)

Structural and magnetic properties of zinc- and aluminum-substituted cobalt ferrite prepared by co-precipitation method. S T ALONE1,∗ and K M JADHAV2. 1Shiv Chhatrapati College, Aurangabad 431 004, India. 2Department of Physics, Dr. B. A. Marathwada University, Aurangabad 431 004, India. ∗Corresponding author.

Selective removal of Cs and Re by precipitation in a Na2CO3-H2O2 solution

International Nuclear Information System (INIS)

Eil-Hee Lee; Jae-Gwan Lim; Dong-Yong Chung; Han-Beom Yang; Kwang-Wook Kim

2010-01-01

The removal of Cs and Re (as a surrogate for Tc) by selective precipitation from the simulated fission products which were co-dissolved with uranium during the oxidative dissolution of spent fuel in a Na 2 CO 3 -H 2 O 2 solution was investigated in this study. The precipitations of Cs and Re were examined by introducing sodium tetraphenylborate (NaTPB) and tetraphenylohosponium chloride (TPPCl), respectively. The precipitation of Cs by NaTPB and that of Re by TPPCl each took place within 5 min, and an increase in temperature up to 50 deg C and a stirring speed up to 1000 rpm hardly affected their precipitation rates. The most important factor in the precipitation with NaTPB and TPPCl was found to be a pH of the solution after precipitation. Since Mo tends to co-precipitate with Cs or Re at a lower pH, an effective precipitation with NaTPB and TPPCl was done at pH of above 9 without the co-precipitation of Mo. More than 99% of Cs and Re were precipitated when the initial concentration ratio of NaTPB to Cs was above 1 and when that of TPPCl to Re was above 1. The precipitation of Cs and Re was never affected by the concentration of Na 2 CO 3 and H 2 O 2 , even though they were raised up to 1.5 and 1.0 M, respectively. Precipitation yields of Cs and Re in a Na 2 CO 3 -H 2 O 2 solution were found to be dependent on the concentration ratios of [NaTBP]/[Cs] and [TPPCl]/[Re]. (author)

Lithium recycling and cathode material regeneration from acid leach liquor of spent lithium-ion battery via facile co-extraction and co-precipitation processes.

Science.gov (United States)

Yang, Yue; Xu, Shengming; He, Yinghe

2017-06-01

A novel process for extracting transition metals, recovering lithium and regenerating cathode materials based on facile co-extraction and co-precipitation processes has been developed. 100% manganese, 99% cobalt and 85% nickel are co-extracted and separated from lithium by D2EHPA in kerosene. Then, Li is recovered from the raffinate as Li 2 CO 3 with the purity of 99.2% by precipitation method. Finally, organic load phase is stripped with 0.5M H 2 SO 4 , and the cathode material LiNi 1/3 Co 1/3 Mn 1/3 O 2 is directly regenerated from stripping liquor without separating metal individually by co-precipitation method. The regenerative cathode material LiNi 1/3 Co 1/3 Mn 1/3 O 2 is miro spherical morphology without any impurities, which can meet with LiNi 1/3 Co 1/3 Mn 1/3 O 2 production standard of China and exhibits good electrochemical performance. Moreover, a waste battery management model is introduced to guarantee the material supply for spent battery recycling. Copyright © 2017 Elsevier Ltd. All rights reserved.

First estimates of the contribution of CaCO3 precipitation to the release of CO2 to the atmosphere during young sea ice growth

Science.gov (United States)

Geilfus, N.-X.; Carnat, G.; Dieckmann, G. S.; Halden, N.; Nehrke, G.; Papakyriakou, T.; Tison, J.-L.; Delille, B.

2013-01-01

report measurements of pH, total alkalinity, air-ice CO2 fluxes (chamber method), and CaCO3 content of frost flowers (FF) and thin landfast sea ice. As the temperature decreases, concentration of solutes in the brine skim increases. Along this gradual concentration process, some salts reach their solubility threshold and start precipitating. The precipitation of ikaite (CaCO3.6H2O) was confirmed in the FF and throughout the ice by Raman spectroscopy and X-ray analysis. The amount of ikaite precipitated was estimated to be 25 µmol kg-1 melted FF, in the FF and is shown to decrease from 19 to 15 µmol kg-1 melted ice in the upper part and at the bottom of the ice, respectively. CO2 release due to precipitation of CaCO3 is estimated to be 50 µmol kg-1 melted samples. The dissolved inorganic carbon (DIC) normalized to a salinity of 10 exhibits significant depletion in the upper layer of the ice and in the FF. This DIC loss is estimated to be 2069 µmol kg-1 melted sample and corresponds to a CO2 release from the ice to the atmosphere ranging from 20 to 40 mmol m-2 d-1. This estimate is consistent with flux measurements of air-ice CO2 exchange. Our measurements confirm previous laboratory findings that growing young sea ice acts as a source of CO2 to the atmosphere. CaCO3 precipitation during early ice growth appears to promote the release of CO2 to the atmosphere; however, its contribution to the overall release by newly formed ice is most likely minor.

Phosphors

International Nuclear Information System (INIS)

1975-01-01

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

Raman Spectra of Luminescent Graphene Oxide (GO-Phosphor Hybrid Nanoscrolls

Directory of Open Access Journals (Sweden)

Janardhanan. R. Rani

2015-12-01

Full Text Available Graphene oxide (GO-phosphor hybrid nanoscrolls were synthesized using a simple chemical method. The GO-phosphor ratio was varied to find the optimum ratio for enhanced optical characteristics of the hybrid. A scanning electron microscope analysis revealed that synthesized GO scrolls achieved a length of over 20 μm with interior cavities. The GO-phosphor hybrid is extensively analyzed using Raman spectroscopy, suggesting that various Raman combination modes are activated with the appearance of a low-frequency radial breathing-like mode (RBLM of the type observed in carbon nanotubes. All of the synthesized GO-phosphor hybrids exhibit an intense luminescent emission around 540 nm along with a broad emission at approximately 400 nm, with the intensity ratio varying with the GO-phosphor ratio. The photoluminescence emissions were gauged using Commission Internationale d'Eclairage (CIE coordinates and at an optimum ratio. The coordinates shift to the white region of the color spectra. Our study suggests that the GO-phosphor hybrid nanoscrolls are suitable candidates for light-emitting applications.

Chemical ore genesis models for the precipitation of carnotite in calcrete

International Nuclear Information System (INIS)

Mann, A.W.

1974-10-01

An investigation was carried out on the chemical mechanism responsible for the precipitation of carnotite in calcrete. The correct interpretation of uranium and vanadium movement in groundwater may only be possible after a careful and detailed evaluation of the occurrence (or non-occurrence) of many other uranium-vanadium complex salts, particularly those of calcium. It is concluded that a redox controlled mechanism for the precipitation of carnotite from groundwaters seem most likely. (R.L.)

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 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).

The Influence of Conditions on Synthesis Hydroxyapatite By Chemical Precipitation Method

Science.gov (United States)

Zhu, Jianping; Kong, Deshuang; Zhang, Yin; Yao, Nengjian; Tao, Yaqiu; Qiu, Tai

2011-10-01

Particles of Hydroxyapatite (HAp) were synthesized by means of chemical precipitation method, under atmosphere pressure. The starting solution with the Ca/P ratio of 1.67 was prepared by mixing 0.167 mol·dm-3 Ca(NO3)2·4H2O, 0.100 mol·dm-3 (NH4)2HPO4, 0.500 mol·dm-3 (NH2)2CO and 0.10 mol·dm-3 HNO3 aqueous solutions. The hydroxyapatite were prepared by heating the solution at 80 °C for 24 hour and then at 90°C for 72 hour. Then followed, the dry powers were heat treatment at 660°C temperatures for 8 hour. The obtained powder was analyzed using XRD, XRF, FT-IR, SEM, TG-DTA. The results showed that obtained HAp powers were greatly influenced by synthetic conditions. HAp powders with various morphologies, such as sphere, rod, layered, dumbbell, fibre, scaly, were obtained by controlling the synthetic conditions.

The Influence of Conditions on Synthesis Hydroxyapatite By Chemical Precipitation Method

International Nuclear Information System (INIS)

Zhu Jianping; Zhang Yin; Yao Nengjian; Tao Yaqiu; Qiu Tai; Kong Deshuang

2011-01-01

Particles of Hydroxyapatite (HAp) were synthesized by means of chemical precipitation method, under atmosphere pressure. The starting solution with the Ca/P ratio of 1.67 was prepared by mixing 0.167 mol·dm −3 Ca(NO 3 ) 2 ·4H 2 O, 0.100 mol·dm −3 (NH 4 ) 2 HPO 4 , 0.500 mol·dm −3 (NH 2 ) 2 CO and 0.10 mol·dm −3 HNO3 aqueous solutions. The hydroxyapatite were prepared by heating the solution at 80 °C for 24 hour and then at 90°C for 72 hour. Then followed, the dry powers were heat treatment at 660°C temperatures for 8 hour. The obtained powder was analyzed using XRD, XRF, FT-IR, SEM, TG-DTA. The results showed that obtained HAp powers were greatly influenced by synthetic conditions. HAp powders with various morphologies, such as sphere, rod, layered, dumbbell, fibre, scaly, were obtained by controlling the synthetic conditions.

[Chemical characteristics of precipitation in South China Sea].

Science.gov (United States)

Xiao, Hong-Wei; Long, Ai-Min; Xie, Lu-Hua; Xiao, Hua-Yun; Liu, Cong-Qiang

2014-02-01

Rainwater samples were collected in the summer on "Shiyan 3" during the 2012 South China Sea Sectional Scientific Survey. The concentrations of anion and cation, and pH in precipitation were determined and backward trajectories of air mass were simulated to analyze the chemical characteristics of ions and examine the source of ions. The results indicated that the mean pH value of precipitation was 6.3, with 5.6 of minimal value in summer in South China Sea. The order of anion and cation abundance was Cl(-) > S04(2-) > NO3(-) and Na(+) > Mg(2+) > Ca(2+) > K(+). Cl(-) was the major anion and Na(+) was the major cation, with concentrations of 2 637.5 microeq x L(-1) and 2095.5 microeq x L(-1), respectively, showing that they were the characteristics of marine atmospheric precipitation. There was a good linear relationship between each pair of 7 ions, with correlation coefficient above 0.9, suggesting that they may have a common source. However, the correlation coefficients were lower between NO3(-) and other ions than the others, suggesting that NO3(-) had more complex sources. The concentrations of Ca(2+) and K(+) in precipitation may be related to coral environment in South China Sea. The backward trajectories in 6 stations showed that the air mass was from south and southwest of South China Sea, without passing through above the continent. These results suggested that precipitation affected by human ion source can be ignored in summer in South China Sea.

Remanence properties of Co-precipitated cobalt ferrite

International Nuclear Information System (INIS)

Bueno-Baques, D.; Medina-Boudri, Angela; Matutes-Aquino, J.

2001-01-01

Isothermal remanent magnetization (IRM) and DC demagnetization (DCD) curves of a co-precipitated cobalt ferrite sample were obtained. From the IRM and DCD data, the Henkel plot was obtained and analyzed in the Preisach model framework. The Henkel plot data are below the Wohlfarth line that indicates a dominant local disorder (demagnetizing-like effect). Forward and reverse switching field distribution curves were obtained from differentiation of the IRM and DCD curves. The peak values of these switching field distributions differ by a factor of about 2.7

Understanding Single-Thread Meandering Rivers with High Sinuosity on Mars through Chemical Precipitation Experiments

Science.gov (United States)

Lim, Y.; Kim, W.

2015-12-01

Meandering rivers are extremely ubiquitous on Earth, yet it is only recently that single-thread experimental channels with low sinuosity have been created. In these recent experiments, as well as in natural rivers, vegetation plays a crucial role in maintaining a meandering pattern by adding cohesion to the bank and inhibiting erosion. The ancient, highly sinuous channels found on Mars are enigmatic because presumably vegetation did not exist on ancient Mars. Under the hypothesis that Martian meandering rivers formed by chemical precipitation on levees and flood plain deposits, we conducted carbonate flume experiments to investigate the formation and evolution of a single-thread meander pattern without vegetation. The flow recirculating in the flume is designed to accelerate chemical reactions - dissolution of limestone using CO2 gas to produce artificial spring water and precipitation of carbonates to increase cohesion- with precise control of water discharge, sediment discharge, and temperature. Preliminary experiments successfully created a single-thread meandering pattern through chemical processes. Carbonate deposits focused along the channel sides improved the bank stability and made them resistant to erosion, which led to a stream confined in a narrow path. The experimental channels showed lateral migration of the bend through cut bank and point bar deposits; intermittent floods created overbank flow and encouraged cut bank erosion, which enhanced lateral migration of the channel, while increase in sediment supply improved lateral point bar deposition, which balanced erosion and deposition rates. This mechanism may be applied to terrestrial single-thread and/or meandering rivers with little to no vegetation or before its introduction to Earth and also provide the link between meandering river records on Mars to changes in Martian surface conditions.

Effects of freshwater Synechococcus sp. cyanobacteria pH buffering on CaCO3 precipitation: Implications for CO2 sequestration

International Nuclear Information System (INIS)

Martinez, Raul E.; Weber, Sebastian; Grimm, Christian

2016-01-01

In the present study, a mixed-flow steady-state bio-reactor was designed to biomineralize CO 2 as a consequence of photosynthesis from active Synechococcus sp. Dissolved CO 2 , generated by constant air bubbling of inorganic and cyanobacteria stock solutions, was the only source of inorganic carbon. The release of hydroxide ion by cyanobacteria from photosynthesis maintained highly alkaline pH conditions. In the presence of Ca 2+ and carbonate species, this led to calcite supersaturation under steady state conditions. Ca 2+ remained constant throughout the experiments showing the presence of steady state conditions. Similarly, the Synechococcus sp. biomass concentration remained stable within uncertainty. A gradual pH decrease was observed for the highest Ca 2+ condition coinciding with the formation of CaCO 3 . The high degree of supersaturation, under steady-state conditions, contributed to the stabilization of calcite and maintained a constant driving force for the mineral nucleation and growth. For the highest Ca 2+ condition a fast crystal growth rate was consistent with rapid calcite precipitation as suggested further by affinity calculations. Although saturation state based kinetic precipitation models cannot accurately reflect the controls on crystal growth kinetics or reliably predict growth mechanisms, the relatively reaction orders obtained from modeling of calcite precipitation rates as function of decreasing carbonate concentration suggest that the precipitation occurred via surface-controlled rate determining reactions. These high reaction orders support in addition the hypothesis that crystal growth proceeded through complex surface controlled mechanisms. In conclusion, the steady state supersaturated conditions generated by a constant cyanobacteria biomass and metabolic activity strongly suggest that these microorganisms could be used for the development of efficient CO 2 sequestration methods in a controlled large-scale environment. - Highlights: �

Current Travertines Precipitation from CO2-rich Groundwaters as an alert of CO2 Leakages from a Natural CO2 Storage at Ganuelas-Mazarron Tertiary Basin (Murcia, Spain)

International Nuclear Information System (INIS)

Rodrigo-Naharro, J.; Delgado, A.; Herrero, M. J.; Granados, A.; Perez del Villar, L.

2013-01-01

Carbon capture and storage technologies represent the most suitable solutions related to the high anthropogenic CO 2 emissions to the atmosphere. As a consequence, monitoring of the possible CO 2 leakages from an artificial deep geological CO 2 storage is indispensable to guarantee its safety. Fast surficial travertine precipitation related to these CO 2 leakages can be used as an alert for these escapes. Since few studies exist focusing on the long-term behaviour of an artificial CO 2 DGS, natural CO 2 storage affected by natural or artificial escapes must be studied as natural analogues for predicting the long-term behaviour of an artificial CO 2 storage. In this context, a natural CO 2 reservoir affected by artificial CO 2 escapes has been studied in this work. This study has mainly focused on the current travertines precipitation associated with the upwelling CO 2 -rich waters from several hydrogeological wells drilled in the Ganuelas-Mazarron Tertiary basin (SE Spain), and consists of a comprehensive characterisation of parent-waters and their associated carbonates, including elemental and isotopic geochemistry, mineralogy and petrography. Geochemical characterisation of groundwaters has led to recognise 4 hydrofacies from 3 different aquifers. These groundwaters have very high salinity and electrical conductivity; are slightly acid; present high dissolved inorganic carbon (DIC) and free CO 2 ; are oversaturated in both aragonite and calcite; and dissolve, mobilize and transport low quantities of heavy and/or toxic elements. Isotopic values indicate that: i) the origin of parent-waters is related to rainfalls from clouds originated in the Mediterranean Sea or continental areas; ii) the origin of C is mainly inorganic; and iii) sulphate anions come mainly from the dissolution of the Messinian gypsum from the Tertiary Basin sediments. Current travertines precipitation seems to be controlled by a combination of several factors, such as: i) a fast decrease of the

Tests for improvement of decontamination factors on RWTP technological line of precipitation

International Nuclear Information System (INIS)

Popovici, C.

1998-01-01

Low and intermediate level radioactive wastes are produced from diverse applications of radionuclides and radioactive materials in industry, medicine, agriculture and research. Many of the liquid wastes need treatment for safe management. Chemical precipitation process is well established for the removal of radioactive from LLW and ILW. The precipitation of insoluble compounds is one of the oldest and most used process for the treatment of aqueous waste. The precipitation can be performed either in a simple step or by combined chemical treatment which mainly includes as radioactive carries iron oxo-hydroxides, iron phosphate, calcium phosphate and cooper ferrocyanide. The contaminants are removed from LLW and ILW during precipitation by different mechanisms such as: coagulation and flocculation process, precipitation and co-precipitation, adsorption on the coagulant aid, ion exchange and physical enmeshment by coagulant aid. All these processes are directly dependent on the precipitate properties and its structure which are connected with the initial system composition and the precipitation procedure. Chemical precipitation method for treatment of LLW and ILW by co-precipitation of caesium with cooper ferrocyanide was employed on the real radioactive wastes where the volumes were 3 m 3 , 24 m 3 and 30 m 3 . The percentage removals of Cs-137 from 2285 Bq, 1310 Bq and 1232 Bq per litre of real effluents were 98.8%, 98.9% and 99.1%, respectively. Test runs for removal of Cs-137 from the wastes varied from 90% to 95%. High decontamination factors were observed in the pH range of 9 to 10.5. (author)

Electrochemical performance of multi-element doped α-nickel hydroxide prepared by supersonic co-precipitation method

International Nuclear Information System (INIS)

Zhang, Z.J.; Zhu, Y.J.; Bao, J.; Lin, X.R.; Zheng, H.Z.

2011-01-01

Highlights: → The α-nickel hydroxides doped with several elements were prepared by supersonic co-precipitation method. → Cyclic voltammetry and electrochemical impedance spectroscopy show sample C has the best electrochemical performance. → The charge/discharge tests show that the 0.5 C discharge capacity (346 mAh/g) of sample C is even larger than that (337 mAh/g) at 0.1 C rate, while the discharge capacity at 0.5 C rate is much lower than that at 0.1 C rate for samples A and B. - Abstract: The multi-element doped α-nickel hydroxides have been prepared by supersonic co-precipitation method. Three kinds of samples A, B, C were prepared by chemically coprecipitating Ni, Al, Co, Y, Zn. It was found that sample C produced better performance than the others. The cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) measurements indicated that sample C has better electrochemical performance, such as better reaction reversibility, higher proton diffusion coefficient and lower charge-transfer resistance, than those of samples A and B. The charge-discharge tests showed that the discharge capacity (346 mA h/g) of sample C is even larger at 0.5 C rate than that (337mAh/g) at 0.1 C rate, while the discharge capacity at 0.5 C rate is much lower than that at 0.1 C rate for samples A and B. It indicates that all doped elements can produce the synergic effect and further improve the electrochemical properties of the active materials.

Encapsulation of albumin in self-assembled layer-by-layer microcapsules: comparison of co-precipitation and adsorption techniques.

Science.gov (United States)

Labala, Suman; Mandapalli, Praveen Kumar; Bhatnagar, Shubhmita; Venuganti, Venkata Vamsi Krishna

2015-01-01

The objective of this study is to prepare and characterize polymeric self-assembled layer-by-layer microcapsules (LbL-MC) to deliver a model protein, bovine serum albumin (BSA). The aim is to compare the BSA encapsulation in LbL-MC using co-precipitation and adsorption methods. In co-precipitation method, BSA was co-precipitated with growing calcium carbonate particles to form a core template. Later, poly(styrene sulfonate) and poly(allylamine hydrochloride) were sequentially adsorbed onto the CaCO3 templates. In adsorption method, preformed LbL-MC were incubated with BSA and encapsulation efficiency is optimized for pH and salt concentration. Free and BSA-encapsulated LbL-MC were characterized using Zetasizer, scanning electron microscopy (SEM), Fourier transform infrared spectroscopy and differential scanning calorimeter. Later, in vitro release studies were performed using dialysis membrane method at pH 4, 7.4 and 9. Results from Zetasizer and SEM showed free LbL-MC with an average size and zeta-potential of 2.0 ± 0.6 μm and 8.1 ± 1.9 mV, respectively. Zeta-potential of BSA-loaded LbL-MC was (-)7.4 ± 0.7 mV and (-)5.7 ± 1.0 mV for co-precipitation and adsorption methods, respectively. In adsorption method, BSA encapsulation in LbL-MC was found to be greater at pH 6.0 and 0.2 M NaCl. Co-precipitation method provided four-fold greater encapsulation efficiency (%) of BSA in LbL-MC compared with adsorption method. At pH 4, the BSA release from LbL-MC was extended up to 120 h. Polyacrylamide gel electrophoresis showed that BSA encapsulated in LBL-MC through co-precipitation is stable toward trypsin treatment. In conclusion, co-precipitation method provided greater encapsulation of BSA in LbL-MC. Furthermore, LbL-MC can be developed as carriers for pH-controlled protein delivery.

Thermoluminescence response of K{sub 2}Ca{sub 2}(SO{sub 4}){sub 3} nanophosphor Co-doped with Eu and Ce for gamma ray dosimetry

Energy Technology Data Exchange (ETDEWEB)

Patil, B. J. [Dept. of Physics, Abasaheb Garware College, Pune-411004 (India); Bhadane, Mahesh S.; Dahiwale, S. S.; Bhoraskar, V. N.; Dhole, S. D., E-mail: sanjay@physics.unipune.ac.in [Department of Physics, University of Pune, Pune 411007 (India); Mandlik, N. T. [Dept. of Physics, Fergusson College, Pune-411004 (India); Kulkarni, M. S. [Radiation Safety Systems Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Bhatt, B. C. [Radiological Physics and Advisory Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India)

2015-06-24

K{sub 2}Ca{sub 2}(SO{sub 4}){sub 3} nanophosphors co-doped with Eu and Ce were synthesized by the chemical co-precipitation method. These samples were further annealed at 700 °C structural reformation. The structural and morphological characteristics were studied using XRD and TEM techniques. The particle size calculated from XRD spectra was around 35 nm. The as synthesized sample shows cubic structure annealed at 700 °C. The as synthesized and annealed sample of K{sub 2}Ca{sub 2}(SO{sub 4}){sub 3}: EuCe were irradiated with Co{sup 60} gamma rays for the doses from 2Gy to 1kGy. The TL characteristic sample of co-doped were studied for the dosimetric application by gamma radiation. The TL spectrum of annealed sample has single peaked at 160 °C. The Eu doped sample has a high TL sensitivity than Ce doped sample. But after co-doping with Eu and Ce, TL intensity observed to be decreased. The decrees in TL peak intensity of the phosphor on co-doping of Eu and Ce gives an insight into the emission mechanism of the phosphor which involves energy transfer from Eu to Ce. The TL response of all the samples were found to be linear for the dose from 2 Gy to 1 KGy. Therefore, K{sub 2}Ca{sub 2}(SO{sub 4}){sub 3}: EuCe nanophosphor can be used for the measurement of high dose of gamma radiation.

Fundamentals of phosphors

CERN Document Server

Yen, William M; Yamamoto, Hajime

2006-01-01

Drawing from the second edition of the best-selling Handbook of Phosphors, Fundamentals of Phosphors covers the principles and mechanisms of luminescence in detail and surveys the primary phosphor materials as well as their optical properties. The book addresses cutting-edge developments in phosphor science and technology including oxynitride phosphors and the impact of lanthanide level location on phosphor performance.Beginning with an explanation of the physics underlying luminescence mechanisms in solids, the book goes on to interpret various luminescence phenomena in inorganic and organic materials. This includes the interpretation of the luminescence of recently developed low-dimensional systems, such as quantum wells and dots. The book also discusses the excitation mechanisms by cathode-ray and ionizing radiation and by electric fields to produce electroluminescence. The book classifies phosphor materials according to the type of luminescence centers employed or the class of host materials used and inte...

Optimisation of parameters for co-precipitation of uranium and plutonium - results of simulation studies

International Nuclear Information System (INIS)

Pandey, N.K.; Velvandan, P.V.; Murugesan, S.; Ahmed, M.K.; Koganti, S.B.

1999-01-01

Preparation of plutonium oxide from plutonium nitrate solution generally proceeds via oxalate precipitation route. In a nuclear fuel reprocessing scheme this step succeeds the partitioning step (separation of uranium and plutonium). Results of present studies confirm that it is possible to avoid partitioning step and recover plutonium and uranium as co-precipitated product. This also helps in minimising the risk of proliferation of fissile material. In this procedure, the solubility of uranium oxalate in nitric acid is effectively used. Co-precipitation parameters are optimised with simulated solutions of uranium nitrate and thorium nitrate (in place of plutonium). On the basis of obtained results a reconversion flow-sheet is designed and reported here. (author)

Influence of Yb{sup 3+} on the structural, dielectric and magnetic properties of Mg{sub 0.7}Co{sub 0.3}Fe{sub 2}O{sub 4} nanocrystallites synthesized via co-precipitation route

Energy Technology Data Exchange (ETDEWEB)

Ejaz, Muhammad [Department of Physics, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Mahmood, Azhar [Department of Chemistry, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Khan, Muhammad Azhar, E-mail: azhar.khan@iub.edu.pk [Department of Physics, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Hussain, Altaf [Department of Physics, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Sultan, Amber [Quaid-e-Azam Medical College, Bahawalpur 63100 (Pakistan); Mahmood, Asif [College of Engineering, Department of Chemical Engineering, King Saud University, Riyadh (Saudi Arabia); Chughtai, Adeel Hussain; Ashiq, Muhammad Naeem [Institute of Chemical Sciences, Bahauddin Zakaryia University, Multan 60800 (Pakistan); Warsi, Muhammad Farooq, E-mail: farooq.warsi@iub.edu.pk [Department of Chemistry, The Islamia University of Bahawalpur, Bahawalpur 63100 (Pakistan); Shakir, Imran [Sustainable Energy Technologies (SET) center, College of Engineering, King Saud University, PO-BOX 800, Riyadh 11421 (Saudi Arabia)

2016-04-15

A series of nanostructured ferrites having chemical composition Mg{sub 0.7}Co{sub 0.3}Yb{sub x}Fe{sub 2−x}O{sub 4} (x=0.0–0.08) was prepared by the chemical co-precipitation route. The synthesized samples were characterized by X-ray diffraction (XRD), Thermo-gravimetric analysis (TGA), differential thermal analysis (DTA), vibrating sample magnetometer (VSM) and impedance analyzer. The analysis of XRD patterns confirmed the spinel structure and the crystallite size calculated by Scherer's formula was found in the range of 18–43 nm. The crystallite size was small enough to obtain considerable signal to noise ratio in the recording media. The lattice constant was increased from 8.362 Ǻ to 8.383 Ǻ as the Yb contents were increased in the magnesium-cobalt ferrites. The TGA and DTA were carried out for prepared sample to investigate the thermal decomposition process. Magnetization results obtained from VSM measurements elucidate that the substitution of rare earth ytterbium decreased the saturation magnetization and retentivity. The dielectric properties of the samples were studied at room temperature in the frequency range of 1 MHz to 3 GHz and the samples exhibited the dispersion in high frequency region. The dielectric constant (ε) and dielectric loss (tan δ) were decreased with the increased frequency and ytterbium doping. The dielectric parameters were explained on the basis of space charge distribution. The dielectric and magnetic parameters suggested that these nano-materials are potential candidates for switching and recording media applications. - Graphical abstract: Mg{sub 0.7}Co{sub 0.3}Yb{sub x}Fe{sub 2−x}O{sub 4} nanostructured spinel ferrites were prepared by chemical co-precipitation technique. The crystallite size was found in the range 18–43 nm. The substitutions of rare earth ytterbium decrease the saturation magnetization and retentivity. The dielectric parameters were explained on the basis of space charge distribution. The

Relationship between 13C and 18O fractionation and changes in major element composition in a recent calcite-depositing spring - a model of chemical variations with inorganic CaCO3 precipitation

International Nuclear Information System (INIS)

Usdowski, E.; Hoefs, J.; Menschel, G.

1979-01-01

A theoretical model is derived in which isotopic fractionations can be calculated as a function of variations in dissolved carbonate species on CO 2 degassing and calcite precipitation. This model is tested by application to a calcite-depositing spring system near Westerhof, Germany. In agreement with the model, 13 C of the dissolved carbonate species changes systematically along the flow path. The difference in delta values between the upper and lower part of the stream is about 1%. The 13 C content of the precipitated calcite is different from that expected from the theoretical partitioning. The isotopic composition of the solid CaCO 3 is similar to that of the dissolved carbonate, though in theory it should be isotopically heavier by about 2.4%. The 18 O composition of dissolved carbonate and H 2 O is constant along the stream. Calculated calcite-water temperatures differ by about +5 0 C from the observed temperatures demonstrating isotopic disequilibrium between the water and precipitated solid. This is attributed to kinetic effects during CaCO 3 deposited from a highly supersaturated solution, in which precipitation is faster than equilibration with respect to isotopes. Plant populations in the water have virtually no influence on CO 2 degassing, calcite saturation and isotopic fractionation. Measurements of Psub(CO 2 ), Ssub(C) and 13 C within a diurnal cycle demonstrate that metabolic effects are below the detection limit in a system with a high supply-rate of dissolved carbonate species. The observed variations are due to differences in CO 2 degassing and calcite precipitation, caused by a continuously changing hydrodynamic conditions and carbonate nucleation rates. (Auth.)

Synthesis and Luminescence Characteristics of Cr³⁺ doped Y₃Al₅O₁₂ Phosphors

Energy Technology Data Exchange (ETDEWEB)

Smith, Brenda A. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Dabestani, Reza T. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Lewis, Linda A. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Thompson, Cyril V. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Collins, Case T. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Aytug, Tolga [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

2015-10-01

Luminescence performance of yttrium aluminum garnet (Y₃Al₅O₁₂) phosphors as a function of Cr³⁺ concentration has been investigated via two different wet-chemical synthesis techniques, direct- (DP) and hydrothermal-precipitation (HP). Using either of these methods, the red-emitting phosphor [Y₃Al_5-xCr_xO₁₂ (YAG: Cr³⁺)] showed similar photoluminescence (PL) intensities once the dopant concentration was optimized. Specifically, the YAG: Cr³⁺ PL emission intensity reached a maximum at Cr3+ concentrations of x = 0.02 (0.4 at.%) and x = 0.13 (2.6 at.%) for DP and HP processed samples, respectively. The results indicated the strong influence of the processing method on the optimized YAG: Cr³⁺ performance, where a more effective energy transfer rate between a pair of Cr3+ activators at low concentration levels was observed by using the DP synthesis technique. Development of a highly efficient phosphor, using a facile synthesis approach, could significantly benefit consumer and industrial applications by improving the operational efficiency of a wide range of practical devices.

Thermoluminescence of calcium-based phosphors

International Nuclear Information System (INIS)

Sunta, C.M.

1985-01-01

The paper reviews the thermoluminescence (TL) properties of calcium fluoride, calcium sulphate and calcium carbonate phosphors. In the case of the calcium fluoride mineral phosphor the main emitter of TL is the cerium impurity. Based on the TL emission spectra, two types of Ce 3+ centres can be easily distinguished; those associated with O 2- compensating ion and those which have either no local compensators or are associated with F - interstitial ions at the adjacent vacant body centre position. The spectra undergo remarkable changes at high doses. Such changes are associated with the probabilities of charge trapping at different types of traps and also with the probabilities of recombination at different types of luminescent centres. Some of the traps and recombination centres are spatially associated while others are distributed randomly. In calcium carbonate mineral, Mn 2+ is invariably the emitting impurity. Mn 2+ can be used as an efficient dopant for TL emission in all the three calcium based TL phosphors. A co-dopant like Ce 3+ intensifies the luminescence yield from Mn 2+ . Models of different types of electron and hole trapping centres are given. (author)

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.)

[Effect of charge compensation on emission spectrum of Sr2SiO4 : Dy3+ phosphor].

Science.gov (United States)

Li, Pan-Lai; Wang, Zhi-Jun; Yang, Zhi-Ping; Guo, Qing-Lin

2009-01-01

The Sr2SiO4 : Dy3+ phosphor was synthesized by the high temperature solid-state reaction method in air. Dy2O3 (99.9%), SiO2 (99.9%), SrCO3 (99.9%), Li2CO3 (99.9%), Na2CO3 (99.9%) and K2CO3 (99.9%) were used as starting materials, and the Dy3+ doping concentration was 2 mol%. The emission spectrum was measured by a SPEX1404 spectrophotometer, and all the characterization of the phosphors was conducted at room temperature. The emission spectrum of Sr2 SiO4 : Dy3+ phosphor showed several bands centered at 486, 575 and 665 nm under the 365 nm excitation. The effect of Li+, Na+ and K+ on the emission spectra of Sr2SiO4 : Dy3+ phosphor was studied. The results show that the location of the emission spectrum of Sr2SiO4 : Dy3+ phosphor was not influenced by Li+, Na+ and K+. However, the emission spectrum intensity was greatly influenced by Li+, Na+ and K+, and the evolvement trend was monotone with different charge compensation, i. e. the emission spectrum intensity of Sr2SiO4 : Dy3+ phosphor firstly increased with increasing Li+ concentration, then decreased. However the charge compensation concentration corresponding to the maximum emission intensity was different with different charge compensation, and the concentration is 4, 3 and 3 mol% corresponding to Li+, Na+ and K+, respectively. And the theoretical reason for the above results was analyzed.

Practical applications of phosphors

CERN Document Server

Yen, William M; Yamamoto, Hajime

2006-01-01

Drawn from the second edition of the best-selling Phosphor Handbook, Practical Applications of Phosphors outlines methods for the production of various phosphors and discusses a broad spectrum of applications. Beginning with methods for synthesis and related technologies, the book sets the stage by classifying and then explaining practical phosphors according to usage. It describes the operating principle and structure of phosphor devices and the phosphor characteristics required for a given device, then covers the manufacturing processes and characteristics of phosphors. The book discusses research and development currently under way on phosphors with potential for practical usage and touches briefly on phosphors that have played a historical role, but are no longer of practical use. It provides a comprehensive treatment of applications including lamps and cathode-ray tubes, x-ray and ionizing radiation, and for vacuum fluorescent and field emission displays and covers inorganic and organic electroluminescen...

Chemical and isotopic composition of precipitations in Syria

International Nuclear Information System (INIS)

Abou Zakhem, B.; Hafez, R.

2008-01-01

13 meteoric stations were selected in syria for cumulative monthly rainfall sampling during two hydrological cycles; 1991-1992 and 1992-1993. The chemical and isotopic compositions of monthly precipitation were studied. The winter and spring rainfall isotopic characteristics were determined, in addition to the syrian or local meteoric line (SMWL) was estimated with a slope of 6.63 and that of both syria and Jordan of 6.73. The effect of climatic factors as temperature and relative air humidity on oxygen-18, deuterium and d-excess were studied and it was found that the relationship between temperature and oxygen-18 and deuterium is a positive linear correlation; however, it is a negative correlation with d-excess. The mean seasonal variation amplitude was determined by 6%, and the amount effect on isotopic content of precipitation was studied. The geographic factors and its affect on isotopic contents of precipitation such as altitude were considered, furthermore, the isotopic gradient with altitude was determined for both oxygen-18 and deuterium (-0.14% and - 0.84%/100 m elevation respectively). The spatial variability of oxygen-18, deuterium, tritium and d-excess indicted the effect of mountain chains and gaps between mountains on the isotopic content of precipitation, the continental effect on tritium build-up by about 33% per 100 Km from the coast. The increase of d-excess values towards the south west proves the eastern mediterranean climate type over this region. (author)

Thermoluminescent properties of CaSO4:Dy prepared by precipitation method

International Nuclear Information System (INIS)

Roman, J.; Rivera, T.; Azorin, J.

2009-10-01

This paper reports the synthesis and thermoluminescent (Tl) characterization of CaSO 4 :Dy obtained by the precipitation method. Thermoluminescent CaSO 4 :Dy powder and Teflon (PTFE) were mixed in order to obtain samples in pellets form. Samples of CaSO 4 :Dy were exposed to a radiation gamma source of 60 Co and 90 Sr beta particles. Tl response of CaSO 4 :Dy showed a glow curve with two peaks centered at around 164 and 302 C. Tl phosphor showed a good linearity in the range from 0.5 to 30 Gy. Fading of the Tl information was 5.19 % in 37 days and presented a standard deviation of 4% for reproducibility. (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.

Co-precipitation synthesis and upconversion luminescence ...

Indian Academy of Sciences (India)

... light: strong green (539 nm), weak red (670 nm) and near-infrared (760 nm). The upconversion luminescence is based on two-photon absorption by the energy transfer from the donor (Yb3+) to the acceptor (Ho3+). All the results indicate that ZrO2:Yb3+-Ho3+ phosphors could be a promising biological labelling material.

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)

Rare earth phosphors and phosphor screens

International Nuclear Information System (INIS)

Buchanan, R.A.; Maple, T.G.; Sklensky, A.F.

1981-01-01

Advances in the use of stabilized rare earth phosphors and of conversion screens using these materials are examined. In particular the new phosphors discussed in this invention consist of oxybromides of yttrium, lanthanum and gadolinium with a luminescent activator ion stabilized by an oxychloride or oxyfluoride surface layer and the conversion screens include trivalent cerium as the activator ion. (U.K.)

Comparison of structural and luminescence properties of Dy2O3 nanopowders synthesized by co-precipitation and green combustion routes

International Nuclear Information System (INIS)

Chandrasekhar, M.; Nagabhushana, H.; Sudheerkumar, K.H.; Dhananjaya, N.; Sharma, S.C.; Kavyashree, D.; Shivakumara, C.; Nagabhushana, B.M.

2014-01-01

Highlights: • Dy 2 O 3 nanopowders were prepared by co-precipitation and eco-friendly green combustion route using plant latex. • Both the products show excellent chromaticity coordinates in the white region, which were quite useful for white LED’s. • Thermoluminescence response of the Dy 2 O 3 product prepared by green synthesis was higher when compared to co-precipitation route. • Structural parameters of Dy 2 O 3 were estimated using Rietveld refinement. • The development of nanosize materials using eco-friendly resources was an attractive non-hazardous chemical route. - Abstract: Dysprosium oxide (Dy 2 O 3 ) nanopowders were prepared by co-precipitation (CP) and eco-friendly green combustion (GC) routes. SEM micrographs prepared by CP route show smooth rods with various lengths and diameters while, GC route show porous, agglomerated particles. The results were further confirmed by TEM. Thermoluminescence (TL) responses of the nanopowder prepared by both the routes were studied using γ-rays. A well resolved glow peak at 353 °C along with less intense peak at 183 °C was observed in GC route while, in CP a single glow peak at 364 °C was observed. The kinetic parameters were estimated using Chen’s glow peak route. Photoluminescence (PL) of Dy 2 O 3 shows peaks at 481, 577, 666 and 756 nm which were attributed to Dy 3+ transitions of 4 F 9/2 ⟶ 6 H 15/2 , 6 H 13/2 , 6 H 11/2 and 6 H 9/2 , respectively. Color co-ordinate values were located in the white region as a result the product may be useful for the fabrication of WLED’S

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.

CO2 chemical valorization

International Nuclear Information System (INIS)

Kerlero De Rosbo, Guillaume; Rakotojaona, Loic; Bucy, Jacques de; Clodic, Denis; Roger, Anne-Cecile; El Khamlichi, Aicha; Thybaud, Nathalie; Oeser, Christian; Forti, Laurent; Gimenez, Michel; Savary, David; Amouroux, Jacques

2014-07-01

Facing global warming, different technological solutions exist to tackle carbon dioxide (CO 2 ) emissions. Some inevitable short term emissions can be captured so as to avoid direct emissions into the atmosphere. This CO 2 must then be managed and geological storage seems to currently be the only way of dealing with the large volumes involved. However, this solution faces major economic profitability and societal acceptance challenges. In this context, alternative pathways consisting in using CO 2 instead of storing it do exist and are generating growing interest. This study ordered by the French Environment and Energy Management Agency (ADEME), aims at taking stock of the different technologies used for the chemical conversion of CO 2 in order to have a better understanding of their development potential by 2030, of the conditions in which they could be competitive and of the main actions to be implemented in France to foster their emergence. To do this, the study was broken down into two main areas of focus: The review and characterization of the main CO 2 chemical conversion routes for the synthesis of basic chemical products, energy products and inert materials. This review includes a presentation of the main principles underpinning the studied routes, a preliminary assessment of their performances, advantages and drawbacks, a list of the main R and D projects underway, a focus on emblematic projects as well as a brief analysis of the markets for the main products produced. Based on these elements, 3 routes were selected from among the most promising by 2030 for an in-depth modelling and assessment of their energy, environmental and economic performances. The study shows that the processes modelled do have favorable CO 2 balances (from 1 to 4 t-CO 2 /t-product) and effectively constitute solutions to reduce CO 2 emissions, despite limited volumes of CO 2 in question. Moreover, the profitability of certain solutions will remain difficult to reach, even with an

Gd doping induced weak ferromagnetic ordering in ZnS nanoparticles synthesized by low temperature co-precipitation technique

Energy Technology Data Exchange (ETDEWEB)

Kaur, Palvinder [Department of Physics, Punjabi University, Patiala, Punjab, 147002 (India); Kumar, Sanjeev, E-mail: sanjeev04101977@gmail.com [Applied Science Department, PEC University of Technology, Chandigarh, 160012 (India); Chen, Chi-Liang, E-mail: chen.cl@nsrrc.org.tw [National Synchrotron Radiation Research Center (NSRRC), Hsinchu, 30076, Taiwan (China); Yang, Kai-Siang [National Synchrotron Radiation Research Center (NSRRC), Hsinchu, 30076, Taiwan (China); Department of Mechanical Engineering, National Taipei University of Technology, Taipei, Taiwan (China); Wei, Da-Hua [Department of Mechanical Engineering, National Taipei University of Technology, Taipei, Taiwan (China); Dong, Chung-Li [Department of Physics, Tamkang University, Tamsui, Taiwan (China); Srivastava, C. [Materials Engineering Department, Indian Institute of Science, Bangalore, 560012 (India); Rao, S.M. [Department of Physics, Punjabi University, Patiala, Punjab, 147002 (India); Institute of Physics, Academia Sinica, Taipei, 11529, Taiwan (China)

2017-01-15

Zn{sub 1−x}Gd{sub x}S nanoparticles with Gd concentration x = 0.00, 0.02 and 0.04 were synthesized by the chemical co-precipitation technique using thioglycerol as capping agent. X-ray diffraction (XRD), transmission electron microscopy (TEM), photoluminescence (PL) spectroscopy, X-ray absorption near-edge structure (XANES) and vibrating sample magnetometer (VSM) were employed to characterize the as synthesized Gd doped ZnS nanoparticles. XRD and TEM studies show the formation of cubic ZnS nanoparticles with an average size in the range 5–10 nm. The doping did not alter the phase of the ZnS. The PL spectra of doped ZnS nanoparticles showed the presence of sulphur vacancies in the lattice. XANES of Gd doped ZnS nanoparticles depicts spectral changes may arise from charge transfer between host Zn and dopant Gd ions. A VSM study shows that the weak ferromagnetic behaviour increases with increase in Gd doping ZnS nanoparticles. - Highlights: • Gd doped ZnS nanoparticles synthesized using co-precipitation technique. • PL studies depict sulphur and zinc vacancies in Gd doped ZnS nanoparticles. • XANES studies depict the charge transfer between host Zn and dopant Gd ions. • Room temperature weak ferromagnetism is observed in Gd doped ZnS nanoparticles.

Gd doping induced weak ferromagnetic ordering in ZnS nanoparticles synthesized by low temperature co-precipitation technique

International Nuclear Information System (INIS)

Kaur, Palvinder; Kumar, Sanjeev; Chen, Chi-Liang; Yang, Kai-Siang; Wei, Da-Hua; Dong, Chung-Li; Srivastava, C.; Rao, S.M.

2017-01-01

Zn_1_−_xGd_xS nanoparticles with Gd concentration x = 0.00, 0.02 and 0.04 were synthesized by the chemical co-precipitation technique using thioglycerol as capping agent. X-ray diffraction (XRD), transmission electron microscopy (TEM), photoluminescence (PL) spectroscopy, X-ray absorption near-edge structure (XANES) and vibrating sample magnetometer (VSM) were employed to characterize the as synthesized Gd doped ZnS nanoparticles. XRD and TEM studies show the formation of cubic ZnS nanoparticles with an average size in the range 5–10 nm. The doping did not alter the phase of the ZnS. The PL spectra of doped ZnS nanoparticles showed the presence of sulphur vacancies in the lattice. XANES of Gd doped ZnS nanoparticles depicts spectral changes may arise from charge transfer between host Zn and dopant Gd ions. A VSM study shows that the weak ferromagnetic behaviour increases with increase in Gd doping ZnS nanoparticles. - Highlights: • Gd doped ZnS nanoparticles synthesized using co-precipitation technique. • PL studies depict sulphur and zinc vacancies in Gd doped ZnS nanoparticles. • XANES studies depict the charge transfer between host Zn and dopant Gd ions. • Room temperature weak ferromagnetism is observed in Gd doped ZnS nanoparticles.

Optical property investigations of polystyrene capped Ca2P2O7:Dy3+ persistent phosphor

International Nuclear Information System (INIS)

Jain, Abhilasha; Kumar, Ashwini; Dhoble, S.J; Peshwe, D.R

2015-01-01

Highlights: • Synthesis of polymer capped pyrophosphate phosphors by citrate gel method. • Radiative lifetime is calculated from parameters of Judd-Ofelt theory and ICP-AES. • Reaction mechanism is discussed leading to high photoluminescence efficiency. • PL emission spectrum reveals broad band emission suitable for solid state lighting. - Abstract: By virtue of enhanced photosensivity, good optical response and better thermal stability, organic–inorganic hybrid materials are contemplated as one of the alternatives for designing advanced optoelectronic devices and innovative photonic applications. A novel inorganic organic hybrid Ca 2 P 2 O 7 :Dy 3+ phosphor has been fabricated by Pechini method. The optical property of synthesized phosphor is successfully altered by the in corporation of polystyrene sulfonic acid as capping agent in the colloidal solution. The phase purity and the average particle size of the prepared phosphor were calculated from X-ray diffraction (XRD) employing Debye Scherrer method. The morphological and chemical investigations were carried out through scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS) analysis. The radiative transitions are explained on the basis of Judd-Ofelt theory and on the basis of derived parameters, the radiative lifetime of persistent hybrid Ca 2 P 2 O 7 :Dy 3+ phosphor is calculated as 5.33 ms. This paper explores the mechanism leading to high photoluminescence efficiency using organic capping additives. The photoluminescence (PL) graphs reveal broad band emission at 482 nm (blue) and 573 nm (yellow) corresponding to 4 F 9/2 - 6 H 15/2 and 4 F 9/2 - 6 H 13/2 transitions of Dy 3+ , respectively. The Commission International De I-Eclairage (CIE) chromaticity co-ordinates were calculated from emission spectra and the values (x, y) were approaching to standard value of white emission. The synthesized pyrophosphate phosphors can thereby account in multiple potential applications

Synthesis and crystallochemical analysis of phosphoric analogue of troegerite

International Nuclear Information System (INIS)

Sidorenko, G.A.; Zhil'tsova, I.G.; Moroz, I.Kh.

1975-01-01

Uranyl phosphate is easily synthesized by adding a 0.36M solution of phosphorous acid of 60degC to a 0.5M solution of uranyle nitrate. The precipitate at pH 0.87-1.10 contains two morphologically different phases - one in the form of quadratic disks (''heavy'' phase) - the other in form of needle-crystals of size up to 0.1 mm (''light'' phase). X-ray analysis determined the ''heavy'' phase as meta-autunite, - the ''light'' phase as uranyl phosphate of composition (UO 2 ):(PO 4 )=3:2. Uranyl phosphate is straw-coloured, its specific weight is 3.45; the luminescence is similar to that of autunite; the refraction index is Nsub(g)=Nsub(m)=1.581; pr=1.570 with a slight pleochroism from light yellow to white; the interference colours are week; the extinction is direct. The chemical analysis of two independently obtained samples of uranyl phosphate was carried out. It led to the crystallo-chemical formula (UO 2 ) 3 (PO 4 ) 2 x 4,8H 2 O. The symmetry and the parameters of the elementary cell of the phosphate are determined: it is a rhombic cell with a=13.11+-0.01A, b=6.98+-0.01A, c=16.91+-0.03A and Z=3. The x-ray density is rho=3.53. The DTA curve shows a higher temperature at the beginning of the dehydration: nearly 120deg compared with the first endoeffect of N-metaautunite which occurs at 50deg. The i.r. spectrum gives a lower symmetry than for N-meta-autunite. The water in the uranyl phosphate is strongly orientated and coupled to the structure. Dumontite which has a ratio (UO 2 ):(PO 4 )=3:2 is found to have a analogous chemical composition to the uranyl phosphate. The parameters b and c are similar in both compounds. The formation of phosphate and the transformation into N-meta-autunite can take place even under natural coditions. The phosphoric analogue of troegerite has the same (UO 2 )/(PO 4 ) ratio but differs in the water content. The structural relations of the two compounds are still unknown

Lecithin-based wet chemical precipitation of hydroxyapatite nanoparticles.

Science.gov (United States)

Michał, Wojasiński; Ewa, Duszyńska; Tomasz, Ciach

Hydroxyapatite Ca 10 (PO 4 ) 6 (OH) 2 nanoparticles have been successfully synthesized by the wet chemical precipitation method at 60 °C in the presence of biocompatible natural surfactant-lecithin. The composition and morphology of nanoparticles of hydroxyapatite synthesized with lecithin (nHAp-PC) was studied by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). Size distribution for nanoparticles was measured by nanoparticle tracking analysis in NanoSight system. We discuss in details influence of lecithin concentration in reaction system on nHAp-PC morphology, as well as on size distributions and suspendability of nanoparticles. Product exhibits crystalline structure and chemical composition of hydroxyapatite, with visible traces of lecithin. Difference in surfactant amounts results in changes in particles morphology and their average size.

Synthesis and Characterization of Carbon nanofibers on Co and Cu Catalysts by Chemical Vapor Deposition

International Nuclear Information System (INIS)

Park, Eunsil; Kim, Jongwon; Lee, Changseop

2014-01-01

This study reports on the synthesis of carbon nanofibers via chemical vapor deposition using Co and Cu as catalysts. In order to investigate the suitability of their catalytic activity for the growth of nanofibers, we prepared catalysts for the synthesis of carbon nanofibers with Cobalt nitrate and Copper nitrate, and found the optimum concentration of each respective catalyst. Then we made them react with Aluminum nitrate and Ammonium Molybdate to form precipitates. The precipitates were dried at a temperature of 110 .deg. C in order to be prepared into catalyst powder. The catalyst was sparsely and thinly spread on a quartz tube boat to grow carbon nanofibers via thermal chemical vapor deposition. The characteristics of the synthesized carbon nanofibers were analyzed through SEM, EDS, XRD, Raman, XPS, and TG/DTA, and the specific surface area was measured via BET. Consequently, the characteristics of the synthesized carbon nanofibers were greatly influenced by the concentration ratio of metal catalysts. In particular, uniform carbon nanofibers of 27 nm in diameter grew when the concentration ratio of Co and Cu was 6:4 at 700 .deg. C of calcination temperature; carbon nanofibers synthesized under such conditions showed the best crystallizability, compared to carbon nanofibers synthesized with metal catalysts under different concentration ratios, and revealed 1.26 high amorphicity as well as 292 m 2 g -1 high specific surface area

As cast precipitation microstructures in twin-roller melt-spun Cu{sub 90}Co{sub 10} alloys

Energy Technology Data Exchange (ETDEWEB)

Núñez-Coavas, H. [Facultad de Matemática, Astronomía y Física, Universidad Nacional de Córdoba, Ciudad Universitaria, 5000 Córdoba (Argentina); Pozo-López, G., E-mail: gpozo@famaf.unc.edu.ar [Facultad de Matemática, Astronomía y Física, Universidad Nacional de Córdoba, Ciudad Universitaria, 5000 Córdoba (Argentina); Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) (Argentina); Instituto de Física Enrique Gaviola – CONICET (Argentina); Condó, A.M. [Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET) (Argentina); Centro Atómico Bariloche, Comisión Nacional de Energía Atómica, Instituto Balseiro, Universidad Nacional de Cuyo, Av. Bustillo 9500, 8400 San Carlos de Bariloche (Argentina); Urreta, S.E. [Facultad de Matemática, Astronomía y Física, Universidad Nacional de Córdoba, Ciudad Universitaria, 5000 Córdoba (Argentina); and others

2016-12-15

As cast Cu{sub 90}Co{sub 10} ribbons rapidly solidified by twin-roller melt spinning, exhibit special microstructure features. This processing method provides scenarios where a different phase selection takes place; coherent Co precipitates form directly from solidification, with neither a spinodal-like composition oscillation nor a discontinuously precipitated laminar phase. Samples are processed at tangential wheel speeds of 10 m/s (V10), 15 m/s (V15), 20 m/s (V20) and 30 m/s (V30). Microstructures resulting from this single step process are characterized and the hysteresis properties and the magnetoresistance effects evaluated. Samples V30 have a quite uniform density of coherent precipitates, with a narrow size distribution around 4 nm. On contrary, non-uniform precipitate distributions are found in samples cooled at lower rates; zones with a high density of coherent Co-rich precipitates are found forming colonies. These colonies are consistent with the extended compositional fluctuations occurring during very early stages in the cooling process. Samples may exhibit wide (V10) and even bimodal (V15) size distributions. Only samples V30 behave close to the ideal superparamagnetism. Samples V20 present relatively large coercivity and relative remanence and behave as an interacting superparamagnet, while the hysteresis loops of ribbons cooled at lower rates exhibit a ferromagnetic contribution in addition to the superparamagnetic-like one. This ferromagnetic component arises from blocked precipitates, larger than the upper bound size for superparamagnetic behavior at 300 K (12 nm). Room temperature magnetoresistance values associated to granular scattering units decrease as the mean precipitate size increases, but they remain below 2%, which is lower than that measured in samples annealed after rapid solidification, indicating that in this latter case contributions from the spinodally segregated matrix take place in addition to that of Co granules. - Highlights: �

Morphology and Kinetics of Growth of CaCO3 Precipitates Formed in Saline Water at 30°C

Science.gov (United States)

Sui, Xin; Wang, Baohui; Wu, Haiming

2018-02-01

The crystallization kinetics and morphology of CaCO3 crystals precipitated from the high salinity oilfield water were studied. The crystallization kinetics measurements show that nucleation and nuclei growth obey the first order reaction kinetics. The induction period of precipitation is extended in the high salinity solutions. Morphological studies show that impurity ions remain mostly in the solution phase instead of filling the CaCO3 crystal lattice. The morphology of CaCO3 precipitates can be changed from a smooth surface (calcite) to rough spheres (vaterite), and spindle rod bundles, or spherical, ellipsoid, flowers, plates and other shapes (aragonite).

Structural stability and elastic properties of L12 Co3(Ga,W) precipitate from first-principle calculations

International Nuclear Information System (INIS)

Yao Qiang; Zhu Yuhong; Wang Yan

2011-01-01

Ultrasoft pseudopotential within a generalized gradient approximation was employed to study the structural stability, electronic structure, and elastic properties of ternary Co 3 (Ga,W) precipitate. The Young's and shear moduli of the polycrystals containing the Co 3 (Ga,W) precipitate were calculated using the Voigt-Reuss-Hill averaging scheme. Results show that the stable ternary Co 3 (Ga,W) compound has the L1 2 structure, and is ductile in nature. The structural stability of the Co 3 (Ga,W) compound is discussed together with the calculated electronic structure.

Contrasting the co-variability of daytime cloud and precipitation over tropical land and ocean

Science.gov (United States)

Jin, Daeho; Oreopoulos, Lazaros; Lee, Dongmin; Cho, Nayeong; Tan, Jackson

2018-03-01

The co-variability of cloud and precipitation in the extended tropics (35° N-35° S) is investigated using contemporaneous data sets for a 13-year period. The goal is to quantify potential relationships between cloud type fractions and precipitation events of particular strength. Particular attention is paid to whether the relationships exhibit different characteristics over tropical land and ocean. A primary analysis metric is the correlation coefficient between fractions of individual cloud types and frequencies within precipitation histogram bins that have been matched in time and space. The cloud type fractions are derived from Moderate Resolution Imaging Spectroradiometer (MODIS) joint histograms of cloud top pressure and cloud optical thickness in 1° grid cells, and the precipitation frequencies come from the Tropical Rainfall Measuring Mission (TRMM) Multi-satellite Precipitation Analysis (TMPA) data set aggregated to the same grid.It is found that the strongest coupling (positive correlation) between clouds and precipitation occurs over ocean for cumulonimbus clouds and the heaviest rainfall. While the same cloud type and rainfall bin are also best correlated over land compared to other combinations, the correlation magnitude is weaker than over ocean. The difference is attributed to the greater size of convective systems over ocean. It is also found that both over ocean and land the anti-correlation of strong precipitation with weak (i.e., thin and/or low) cloud types is of greater absolute strength than positive correlations between weak cloud types and weak precipitation. Cloud type co-occurrence relationships explain some of the cloud-precipitation anti-correlations. Weak correlations between weaker rainfall and clouds indicate poor predictability for precipitation when cloud types are known, and this is even more true over land than over ocean.

Impact of location of CaCO3 precipitation on the development of intact anaerobic sludge

NARCIS (Netherlands)

Langerak, van E.P.A.; Ramaekers, H.; Wiechers, J.; Veeken, A.H.M.; Hamelers, H.V.M.; Lettinga, G.

2000-01-01

The development of intact anaerobic granular sludge was studied in UASB reactors under varying conditions of CaCO3 precipitation and biomass yield. Varying precipitating quantities were obtained using different calcium concentrations in the influent and different biomass yields were obtained by

Current Travertines Precipitation from CO{sub 2}-rich Groundwaters as an alert of CO{sub 2} Leakages from a Natural CO{sub 2} Storage at Ganuelas-Mazarron Tertiary Basin (Murcia, Spain)

Energy Technology Data Exchange (ETDEWEB)

Rodrigo-Naharro, J.; Delgado, A.; Herrero, M. J.; Granados, A.; Perez del Villar, L.

2013-02-01

Carbon capture and storage technologies (CCS) represent the most suitable solutions related to the high anthropogenic CO{sub 2} emissions to the atmosphere. As a consequence, monitoring of the possible CO{sub 2} leakages from an artificial deep geological CO{sub 2} storage (DGS) is indispensable to guarantee its safety. Fast surficial travertine precipitation related to these CO{sub 2} leakages can be used as an alert for these escapes. Since few studies exist focusing on the long-term behaviour of an artificial CO{sub 2} DGS, natural CO{sub 2} storage affected by natural or artificial escapes must be studied as natural analogues for predicting the long-term behaviour of an artificial CO{sub 2} storage. In this context, a natural CO{sub 2} reservoir affected by artificial CO{sub 2} escapes has been studied in this work. This study has mainly focused on the current travertines precipitation associated with the upwelling CO{sub 2}-rich waters from several hydrogeological wells drilled in the Ganuelas-Mazarron Tertiary basin (SE Spain), and consists of a comprehensive characterisation of parent-waters and their associated carbonates, including elemental and isotopic geochemistry, mineralogy and petrography. Geochemical characterisation of groundwaters has led to recognise 4 hydrofacies from 3 different aquifers. These groundwaters have very high salinity and electrical conductivity; are slightly acid; present high dissolved inorganic carbon (DIC) and free CO{sub 2}; are oversaturated in both aragonite and calcite; and dissolve, mobilize and transport low quantities of heavy and/or toxic elements. Isotopic values indicate that: i) the origin of parent-waters is related to rainfalls from clouds originated in the Mediterranean Sea or continental areas; ii) the origin of C is mainly inorganic; and iii) sulphate anions come mainly from the dissolution of the Messinian gypsum from the Tertiary Basin sediments. Current travertines precipitation seems to be controlled by a

Blue emitting KSCN:xCe phosphor for solid state lighting

Energy Technology Data Exchange (ETDEWEB)

Chikte, Devayani, E-mail: devi.awade@gmail.com [G.N. Khalsa College, Matunga, Mumbai 400019 (India); Omanwar, S.K. [Department of Physics, S.G.B. Amravati University, Amravati (India); Moharil, S.V. [Department of Physics, R.T.M. Nagpur University, Nagpur 440010 (India)

2014-01-15

The intense blue emitting phosphor KSCN:xCe (x=0.005, 0.01, 0.02, 0.04) is synthesized by a simple, time saving, economical method of re-crystallization through aqueous solution at 353 K. Photoluminescence measurements showed that the said phosphor exhibits emission with good intensity peaking at 450 nm corresponding to d→f transitions of Ce{sup 3+} ion. The excitation spectra monitored at 450 nm shows small peak at 282 nm and broad intense excitation band peaking at 350 nm. The latter lies in near ultraviolet (350–410 nm) emission of UV LED. The phosphor KSCN:0.02Ce{sup 3+} shows CIE 1931 color coordinates as (0.1484, 0.0602) whereas the commercial blue phosphor BAM:Eu{sup 2+} shows the color co-ordinates as (0.1417, 0.1072), respectively, indicating better color purity for KSCN: 0.02Ce{sup 3+} compared to the BAM:Eu{sup 2+} phosphor. The color coordinates of KSCN: 0.02Ce{sup 3+} phosphor (0.1484, 0.0602) are nearer to the color coordinate for blue color suggested by the color systems EBUPAL/SECAM, sRGB Blue as well as Adobe blue(0.15, 0.06). -- Highlights: • Novel phosphor KSCN:xCe prepared for the first time. • Method is simple, time saving, economical, easy to handle. • Intense, blue, Characteristic Ce{sup 3+} emission at 450 nm. • nUV excitation, suitable for solid state lighting.

CO_2 valorization - Part. 2: chemical transformation ways

International Nuclear Information System (INIS)

Dumergues, Laurent

2016-01-01

Carbon dioxide (CO_2) can be used in many ways as a raw material or chemical reagent. The chemical conversion of CO_2 used as a feedstock is achievable by different techniques: mineralization, organic synthesis, hydrogenation, dry reforming, electrolysis, thermolysis, etc. The products obtained have applications as energy products, chemicals, building materials, etc. Choosing an appropriate CO_2 reuse technology will depend on technical and economic requirements (such as the CO_2 purity needed, technological maturity, cost-effectiveness, etc.) and also environmental and social criteria

Chemical and isotopic composition of precipitations in Syria

International Nuclear Information System (INIS)

Abou Zakhem, B.; Hafez, R.

2007-05-01

The objective of this study is to determine isotopic characteristics of precipitation, the climatic and geographical conditions affecting isotopic composition in order to obtain the input function of groundwater to evaluate the water resources.13 meteoric stations were selected in Syria for cumulative monthly rainfall sampling during two hydrological cycles; 1991-1992 and 1992-1993. The chemical and isotopic compositions of monthly precipitation were studied. The winter and spring rainfall isotopic characteristics were determined, in addition to the Syrian meteoric line (SMWL) was estimated with a slope of 6.62 and that of both Syria and Jordan of 6.73. The effect of climatic factors as temperature and relative air humidity on oxygen-18, deuterium and d-excess were studied and it was found that the relationship between temperature and oxygen-18 and deuterium is a positive linear correlation; however, it is a negative correlation with d-excess. The mean seasonal variation amplitude of 18 O was about 6%, and the amount effect on isotopic content of precipitation was studied. The geographic factors and its affect on isotopic contents of precipitation such as altitude were considered, furthermore, the isotopic gradient with altitude was determined for both oxygen-18 and deuterium (-0.14 % and -0.84% /100m respectively). The spatial distribution of oxygen-18, deuterium, tritium and d-excess indicted the effect of mountain chains and gaps between mountains on the isotopic content, the continental effect on tritium build-up by about 33% per 100 Km from the coast. The increase of d-excess values towards the south west proves the eastern Mediterranean climate type over this region.(author)

High Extraction Phosphors for Solid State Lighting

Energy Technology Data Exchange (ETDEWEB)

Summers, Chris [Phosphortech Corporation, Kennesaw, GA (United States); Menkara, Hisham [Phosphortech Corporation, Kennesaw, GA (United States); Wagner, Brent [Phosphortech Corporation, Kennesaw, GA (United States)

2011-09-01

We have developed high-index, high efficiency bulk luminescent materials and novel nano-sized phosphors for improved solid-state white LED lamps. These advances can potentially contribute to reducing the loss in luminous efficiencies due to scattering, re-absorption, and thermal quenching. The bulk and nanostructured luminescent materials investigated are index matched to GaN and have broad and size-tunable absorption bands, size and impurity tuned emission bands, size-driven elimination of scattering effects, and a separation between absorption and emission bands. These innovations were accomplished through the use of novel synthesis techniques suitable for high volume production for LED lamp applications. The program produced a full-color set of high quantum yield phosphors with high chemical stability. In the bulk phosphor study, the ZnSeS:Cu,Ag phosphor was optimized to achieve >91% efficiency using erbium (Er) and other activators as sensitizers. Detailed analysis of temperature quenching effects on a large number of ZnSeS:Cu,Ag,X and strontium- and calcium-thiogallate phosphors lead to a breakthrough in the understanding of the anti-quenching behavior and a physical bandgap model was developed of this phenomena. In a follow up to this study, optimized phosphor blends for high efficiency and color performance were developed and demonstrated a 2-component phosphor system with good white chromaticity, color temperature, and high color rendering. By extending the protocols of quantum dot synthesis, large nanocrystals, greater than 20 nm in diameter were synthesized and exhibited bulk-like behavior and blue light absorption. The optimization of ZnSe:Mn nanophosphors achieved ~85% QE The limitations of core-shell nanocrystal systems were addressed by investigating alternative deltadoped structures. To address the manufacturability of these systems, a one-pot manufacturing protocol was developed for ZnSe:Mn nanophosphors. To enhance the stability of these material

Luminescence and energy transfer mechanism in Eu{sup 3+}/Tb{sup 3+}-co-doped ZrO{sub 2} nanocrystal rods

Energy Technology Data Exchange (ETDEWEB)

Ahemen, I., E-mail: ahemior@gmail.com; Dejene, F. B. [University of the Free State-QwaQwa Campus, Department of Physics (South Africa)

2017-01-15

Nanocrystal rods of Eu{sup 3+}/Tb{sup 3+}-co-doped ZrO{sub 2} were synthesized using a simple chemical precipitation technique. Both ions were successfully doped into the Zr{sup 4+} ion site in a mixed structure containing both monoclinic and tetragonal phases. The Eu{sup 3+} or Tb{sup 3+} singly doped zirconia produced red and green luminescence which are characteristics of Eu{sup 3+} and Tb{sup 3+} ions, respectively. The co-doped zirconia samples produced blue emission from defect states transitions in the host ZrO{sub 2}, red and green luminescence from dopant ions giving cool to warm white light emissions. The phosphors were efficiently excited by ultraviolet and near-ultraviolet/blue radiations giving white and red light, respectively. The decay lifetime was found to increase with increasing donor ion concentration contrary to conventional observations reported by previous researchers. Weak quadrupole–quatdrupole multipolar process was responsible for energy transfer from Tb{sup 3+} (donor) ion to Eu{sup 3+} ion. No energy back-transfer from Eu{sup 3+} to Tb{sup 3+} ion was observed from the excitation spectra. Temperature-dependent photoluminescence shows the presence of defects at low temperature, but these defects vanished at room temperature and beyond. The Eu{sup 3+}/Tb{sup 3+}-co-doped ZrO{sub 2} nanocrystal rod is a potential phosphor for white light application using UV as an excitation source. Thermoluminescence measurements show that the inclusion of Tb{sup 3+} ion increases trap depths in the host zirconia.

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

Pharmaceuticals and other anthropogenic chemicals in atmospheric particulates and precipitation.

Science.gov (United States)

Ferrey, Mark L; Coreen Hamilton, M; Backe, Will J; Anderson, Kurt E

2018-01-15

Air and precipitation samples were analyzed by liquid chromatography tandem mass spectrometry (LC-MS/MS) and gas chromatography mass spectrometry (GC-MS) for pharmaceuticals, personal care products, and other commercial chemicals within the St. Paul/Minneapolis metropolitan area of Minnesota, U.S. Of the 126 chemicals analyzed, 17 were detected at least once. Bisphenol A, N,N-diethyl-meta-toluamide (DEET), and cocaine were the most frequently detected; their maximum concentrations in snow were 3.80, 9.49, and 0.171ng/L and in air were 0.137, 0.370, and 0.033ng/m 3 , respectively. DEET and cocaine were present in samples of rain up to 14.5 and 0.806ng/L, respectively. Four antibiotics - ofloxacin, ciprofloxacin, enrofloxacin, and sulfamethoxazole - were detected at concentrations up to 10.3ng/L in precipitation, while ofloxacin was the sole antibiotic detected in air at 0.013ng/m 3 . The X-ray contrast agent iopamidol and the non-steroidal anti-inflammatory drug naproxen were detected in snow up to 228ng/L and 3.74ng/L, respectively, while caffeine was detected only in air at 0.069 and 0.111ng/m 3 . Benzothiazole was present in rain up to 70ng/L, while derivatives of benzotriazole - 4-methylbenzotriazole, 5-methylbenzotriazole, and 5-chlorobenzotriazole - were detected at concentrations up to 1.5ng/L in rain and 3.4ng/L in snow. Nonylphenol and nonylphenol monoethoxylate were detected once in air at 0.165 and 0.032ng/m 3 , respectively. Although the sources of these chemicals to atmosphere are not known, fugacity analysis suggests that wastewater may be a source of nonylphenol, nonylphenol monoethoxylate, DEET, and caffeine to atmosphere. The land-spreading of biosolids is known to generate PM10 that could also account for the presence of these contaminants in air. Micro-pollutant detections in air and precipitation are similar to the profile of contaminants reported previously for surface water. This proof of concept study suggests that atmospheric transport of

Apparatus and methods for regeneration of precipitating solvent

Science.gov (United States)

Liu, Guohai; Vimalchand, Pannalal; Peng, Wan Wang; Bonsu, Alexander

2015-08-25

A regenerator that can handle rich loaded chemical solvent containing precipitated absorption reaction products is disclosed. The invention is particularly suitable for separating CO.sub.2 from large gas streams that are typical of power plant processes. The internally circulating liquid stream in the regenerator (ICLS regenerator) rapidly heats-up the in-coming rich solvent stream in a downcomer standpipe as well as decreases the overall concentration of CO.sub.2 in the mixed stream. Both these actions lead to dissolution of precipitates. Any remaining precipitate further dissolves as heat is transferred to the mixed solution with an inverted bayonet tube heat exchanger in the riser portion of the regenerator. The evolving CO.sub.2 bubbles in the riser portion of the regenerator lead to substantial gas hold-up and the large density difference between the solutions in the downcomer standpipe and riser portions promotes internal circulation of the liquid stream in the regenerator. As minor amounts of solvent components present in the exit gas stream are condensed and returned back to the regenerator, pure CO.sub.2 gas stream exits the disclosed regenerator and condenser system.

Electroluminescent efficiency of alternating current thick film devices using ZnS:Cu,Cl phosphor

International Nuclear Information System (INIS)

Sharma, Gaytri; Han, Sang Do; Kim, Jung Duk; Khatkar, Satyender P.; Rhee, Young Woo

2006-01-01

ZnS:Cu,Cl phosphor is prepared with the help of low intensity milling of the precursor material in two step firing process. The synthesized phosphor is used for the preparation of alternating current thick film electroluminescent (ACTFEL) devices with screen-printing method. The commission international de l'Eclairge (CIE) color co-ordinates of the ACTFEL devices prepared by these phosphor layers shows a shift from bluish-green to green region with the change in the amount of Cu in the phosphor. The various parameters to improve the efficiency and luminance of the devices have also been investigated. The brightness of the ac thick film EL device depends on the particle size of the phosphor, crystallinity, amount of binding material and applied voltage. The EL device fabricated with phosphor having average particle size of 25 μm shows maximum luminescence, when 60% phosphor concentration is used with respect to binding material. EL intensity is also linearly dependent on frequency. It is due the increase of excitation chances of the host matrix or dopant ions with increasing frequency

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

Electronic Transmutation (ET): Chemically Turning One Element into Another.

Science.gov (United States)

Zhang, Xinxing; Lundell, Katie A; Olson, Jared K; Bowen, Kit H; Boldyrev, Alexander I

2018-03-08

The concept of electronic transmutation (ET) depicts the processes that by acquiring an extra electron, an element with the atomic number Z begins to have properties that were known to only belong to its neighboring element with the atomic number Z+1. Based on ET, signature compounds and chemical bonds that are composed of certain elements can now be designed and formed by other electronically transmutated elements. This Minireview summarizes the recent developments and applications of ET on both the theoretical and experimental fronts. Examples on the ET of Group 13 elements into Group 14 elements, Group 14 elements into Group 15 elements, and Group 15 elements into Group 16 elements are discussed. Compounds and chemical bonding composed of carbon, silicon, germanium, phosphorous, oxygen and sulfur now have analogues using transmutated boron, aluminum, gallium, silicon, nitrogen, and phosphorous. © 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Inhibition of precipitation of carbonate apatite by trisodium citrate analysed in base of the formation of chemical complexes in growth solution

Energy Technology Data Exchange (ETDEWEB)

Prywer, Jolanta, E-mail: jolanta.prywer@p.lodz.pl [Institute of Physics, Lodz University of Technology, ul. Wólczańska 219, 93-005 Łódź (Poland); Olszynski, Marcin [Institute of Physics, Lodz University of Technology, ul. Wólczańska 219, 93-005 Łódź (Poland); Mielniczek-Brzóska, Ewa [Institute of Chemistry, Environment Protection and Biotechnology, Jan Długosz University of Częstochowa, ul. Armii Krajowej 13/15, 42-200 Częstochowa (Poland)

2015-11-15

Effect of trisodium citrate on the precipitation of carbonate apatite is studied. The experimental series are performed in the solution of artificial urine. The investigations are related to infectious urinary stones formation as carbonate apatite is one of the main components of this kind of stones. To mimic a real infection in urinary tract the aqueous ammonia solution was added to the solution of artificial urine. The spectrophotometric results demonstrate that trisodium citrate increases induction time with respect to carbonate apatite formation and decreases the efficiency of carbonate apatite precipitation. The inhibitory effect of trisodium citrate on the precipitation of carbonate apatite is explained in base of chemical speciation analysis. Such an analysis demonstrates that the inhibitory effect is mainly related with the fact that trisodium citrate binds Ca{sup 2+} ions and causes the formation of CaCit{sup −} and Ca{sub 10}(PO{sub 4}){sub 6}CO{sub 3} complexes. Trisodium citrate binds Ca{sup 2+} ions in the range of pH from 6 to 9.5 for which carbonate apatite is favored to be formed. - Highlights: • Trisodium citrate (TC) increases induction time of carbonate apatite (CA) formation. • TC decreases the efficiency of CA precipitation. • The inhibitory effect of TC is explained in base of chemical speciation analysis. • The inhibitory effect is mainly related with the fact that TC binds Ca{sup 2+} ions. • TC binds Ca{sup 2+} ions in the range of pH from 6 to 9.5 for which CA is formed.

Phosphors for LED lamps

Science.gov (United States)

Murphy, James Edward; Manepalli, Satya Kishore; Kumar, Prasanth Nammalwar

2013-08-13

A phosphor, a phosphor blend including the phosphor, a phosphor prepared by a process, and a lighting apparatus including the phosphor blend are disclosed. The phosphor has the formula (Ca.sub.1-p-qCe.sub.pK.sub.q).sub.xSc.sub.y(Si.sub.1-rGa.sub.r).sub.zO.su- b.12+.delta. or derived from a process followed using disclosed amounts of reactants. In the formula, (0

Experimental evidence for carbonate precipitation and CO 2 degassing during sea ice formation

Science.gov (United States)

Papadimitriou, S.; Kennedy, H.; Kattner, G.; Dieckmann, G. S.; Thomas, D. N.

2004-04-01

Chemical and stable carbon isotopic modifications during the freezing of artificial seawater were measured in four 4 m 3 tank incubations. Three of the four incubations were inoculated with a nonaxenic Antarctic diatom culture. The 18 days of freezing resulted in 25 to 27 cm thick ice sheets overlying the residual seawater. The ice phase was characterized by a decrease in temperature from -1.9 to -2.2°C in the under-ice seawater down to -6.7°C in the upper 4 cm of the ice sheet, with a concurrent increase in the salinity of the under-ice seawater and brine inclusions of the ice sheet as a result of physical concentration of major dissolved salts by expulsion from the solid ice matrix. Measurements of pH, total dissolved inorganic carbon (C T) and its stable isotopic composition (δ 13C T) all exhibited changes, which suggest minimal effect by biological activity during the experiment. A systematic drop in pH and salinity-normalized C T by up to 0.37 pH SWS units and 376 μmol C kg -1 respectively at the lowest temperature and highest salinity part of the ice sheet were coupled with an equally systematic 13C enrichment of the C T. Calculations based on the direct pH and C T measurements indicated a steady increase in the in situ concentration of dissolved carbon dioxide (CO 2(aq)) with time and increasing salinity within the ice sheet, partly due to changes in the dissociation constants of carbonic acid in the low temperature-high salinity range within sea ice. The combined effects of temperature and salinity on the solubility of CO 2 over the range of conditions encountered during this study was a slight net decrease in the equilibrium CO 2(aq) concentration as a result of the salting-out overriding the increase in solubility with decreasing temperature. Hence, the increase in the in situ CO 2(aq) concentration lead to saturation or supersaturation of the brine inclusions in the ice sheet with respect to atmospheric pCO 2 (≈3.5 × 10 -4 atm). When all physico-chemical

Precipitates/Salts Model Sensitivity Calculation

International Nuclear Information System (INIS)

Mariner, P.

2001-01-01

The objective and scope of this calculation is to assist Performance Assessment Operations and the Engineered Barrier System (EBS) Department in modeling the geochemical effects of evaporation on potential seepage waters within a potential repository drift. This work is developed and documented using procedure AP-3.12Q, ''Calculations'', in support of ''Technical Work Plan For Engineered Barrier System Department Modeling and Testing FY 02 Work Activities'' (BSC 2001a). The specific objective of this calculation is to examine the sensitivity and uncertainties of the Precipitates/Salts model. The Precipitates/Salts model is documented in an Analysis/Model Report (AMR), ''In-Drift Precipitates/Salts Analysis'' (BSC 2001b). The calculation in the current document examines the effects of starting water composition, mineral suppressions, and the fugacity of carbon dioxide (CO 2 ) on the chemical evolution of water in the drift

Separation of Co(II) from dilute aqueous solutions by precipitate and adsorbing colloid flotation

International Nuclear Information System (INIS)

Aziz, M.; Benyamin, K.; Shakir, K.; Atomic Energy Establishment, Cairo

1993-01-01

Ion, precipitate and adsorbing colloid flotation of cobalt(II) have been investigated at different pH values, using N-dodecylpyridinium chloride (DPCl). A strong cationic surfactant, and sodium lauryl sulfate (NaLS), a strong anionic surfactant, as collectors. In case of adsorbing colloid flotation, hydrous manganese dioxide was used as an adsorbent. The precipitate flotation curves experimentally obtained with the two tested collectors were compared with the corresponding theoretical one calculated from the data published for Co(II) hydrolysis. The effects of the collector concentration, ageing of the water-MnO 2 -Co(II) system, bubbling time period, cobalt(II) concentration and foreign salts on the percent removal of Co(II) by adsorbing colloid flotation using DPCl as collector were determined. Removals approaching 100% could be achieved under the optimum conditions. (author) 44 refs.; 6 figs

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.

Study of lithium extraction from brine water, Bledug Kuwu, Indonesia by the precipitation series of oxalic acid and carbonate sodium

Science.gov (United States)

Sulistiyono, Eko; Lalasari, Latifa Hanum; Mayangsari, W.; Prasetyo, A. B.

2018-05-01

Lithium is one of the key elements in the development of batteries for electric car applications. Currently, the resources of the world's lithium are derived from brine water and lithium mineral based on spodumene rock. Indonesia which is located in the area of the ring of fire, has potential brine water resources in some area, such as brine water from Bledug Kuwu, Central Java that used in this research. The purposes of this research are to characterize brine water, Bledug Kuwu and to investigate the influence of chemical solvents on Li, Na, K, Ca, Mg, Al, B ion precipitation from brine water. This research was done with 2 times the process of chemical precipitation that runs series as follows: 5 liters of brine water were chemically precipitated using 400 ml of 12.43 N oxalic acid and followed by chemical precipitation using 400 mL of 7.07 N sodium carbonate solutions. Evaporation and filtration processes were also done twice in an effort to separate white precipitate and filtrate. The filtrate was analyzed by ICP-OES and white precipitates (salts) were analyzed by SEM, XRD, and XRF. The result shows that oxalate precipitation process extracted 32.24% Al, 23.42% B, 22.43% Ca, 14.26% Fe, 3.21 % K, 9.86% Na and 14.26% Li, the following process by carbonate precipitation process extracted 98.86% Mg, 73% Ca, 22.53% Li, 82.04% Al, 14.38% B, 12.50% K, 2.27% Na. There is 63.21% lithium is not extracted from the series process. The SEM analysis shows that the structure of granules on the precipitated salts by oxalic acid form gentle cubic-shaped solid. In the other hand, oxalate precipitation followed by sodium carbonate has various particle sizes and the shape of crystals is fragments, prism and cube look like magnesium carbonate, calcium chloride, and calcite's crystal respectively. This is in accordance with XRD analysis that phases of whewellite (CaC2O4.H2O), disodium oxalate (Na2C2O4), magnesite (MgCO3), calcium lithium aluminum (Al1.19 Ca1Li0.81), dolomite (CaCO3

Effect of land cover, stream discharge, and precipitation on water quality in Puerto Rico

Science.gov (United States)

Hall, J. S.; Uriarte, M.

2017-12-01

In 2015, Puerto Rico experienced one of the worst droughts in its history, causing widespread water rationing and sparking concerns for future resources. The drought represents precipitation extremes that provide valuable insight into the effects of land cover (LC), on modulating discharge and water quality indices at varying spatial scales. We used data collected from 38 water quality and 55 precipitation monitoring stations in Puerto Rico from 2005 to 2016, paired with a 2010 land cover map to (1) determine whether temporal variability in discharge, precipitation, or antecedent precipitation was a better predictor of water quality, (2) find the spatial scale where LC has the greatest impact on water quality, and (3) quantify impacts of LC on water quality indices, including dissolved oxygen (mg/L), total nitrogen (mg/L), phosphorous (mg/L), turbidity (NTRU), fecal coliforms (colony units/100mL) and instantaneous discharge (ft3/s). The resulting linear mixed effects models account for between 36-68% of the variance in water quality. Preliminary results indicate that phosphorous and nitrogen were best predicted from instantaneous stream discharge, the log of discharge was the better predictor for turbidity and fecal coliforms, and summed 2 and 14-day antecedent precipitation indices were better predictors for dissolved oxygen and discharge, respectively. Increased urban and pasture area reliably decreased water quality in relation to forest cover, while agriculture and wetlands had little or mixed effects. Turbidity and nitrogen responded to a watershed level LC, while phosphorous, fecal coliforms, and discharge responded to LC in 60 m riparian buffers at the watershed scale. Our results indicate that LC modulates changing precipitation regimes and the ensuing impacts on water quality at a range of spatial scales.

Study of UO2-10WT%Gd2O3 fuel pellets obtained by seeding method using AUC co-precipitation and mechanical mixing processes

International Nuclear Information System (INIS)

Lima, M.M.F.; Ferraz, W.B.A.; Santos, M.M. dos; Pinto, L.C.M.; Santos, A.

2008-01-01

The use of gadolinium and uranium mixed oxide as a nuclear fuel aims to obtain a fuel with a performance better than that of UO 2 fuel. In this work, seeding method was used to improve ionic diffusivity during sintering to produce high density pellets containing coarse grains by co-precipitation and mechanical mixing processes. Sintered UO 2 -10 wt% Gd 2 O 3 pellets were obtained using the reference processes with 2 wt% and 5 wt% UO 2 seeds with two granulometries, less than 20 μm and between 20 and 38 μm. Characterisation was carried out by chemical analysis, surface area, X-ray diffraction, SEM, WDS, image analysis, and densitometry. The seeding method using mechanical mixing process was more effective than the co-precipitation method. Furthermore, mechanical mixing process resulted in an increase in density of UO 2 -10wt% Gd 2 O 3 with seeds in relation to that of UO 2 -10wt% Gd 2 O 3 without seeds. (author)

Choice of precipitant and calcination temperature of precursor for synthesis of NiCo2O4 for control of CO-CH4 emissions from CNG vehicles.

Science.gov (United States)

Trivedi, Suverna; Prasad, Ram

2018-03-01

Compressed natural gas (CNG) is most appropriate an alternative of conventional fuel for automobiles. However, emissions of carbon-monoxide and methane from such vehicles adversely affect human health and environment. Consequently, to abate emissions from CNG vehicles, development of highly efficient and inexpensive catalysts is necessary. Thus, the present work attempts to scan the effects of precipitants (Na 2 CO 3 , KOH and urea) for nickel cobaltite (NiCo 2 O 4 ) catalysts prepared by co-precipitation from nitrate solutions and calcined in a lean CO-air mixture at 400°C. The catalysts were used for oxidation of a mixture of CO and CH 4 (1:1). The catalysts were characterized by X-ray diffractometer, Brunauer-Emmett-Teller surface-area, X-ray photoelectron spectroscopy; temperature programmed reduction and Scanning electron microscopy coupled with Energy-Dispersive X-Ray Spectroscopy. The Na 2 CO 3 was adjudged as the best precipitant for production of catalyst, which completely oxidized CO-CH 4 mixture at the lowest temperature (T 100 =350°C). Whereas, for catalyst prepared using urea, T 100 =362°C. On the other hand the conversion of CO-CH 4 mixture over the catalyst synthesized by KOH limited to 97% even beyond 400°C. Further, the effect of higher calcination temperatures of 500 and 600°C was examined for the best catalyst. The total oxidation of the mixture was attained at higher temperatures of 375 and 410°C over catalysts calcined at 500 and 600°C respectively. Thus, the best precipitant established was Na 2 CO 3 and the optimum calcination temperature of 400°C was found to synthesize the NiCo 2 O 4 catalyst for the best performance in CO-CH 4 oxidation. Copyright © 2017. Published by Elsevier B.V.

Attenuation of Chemical Reactivity of Shale Matrixes following Scale Precipitation

Science.gov (United States)

Li, Q.; Jew, A. D.; Kohli, A. H.; Alalli, G.; Kiss, A. M.; Kovscek, A. R.; Zoback, M. D.; Brown, G. E.; Maher, K.; Bargar, J.

2017-12-01

Introduction of fracture fluids into shales initiates a myriad of fluid-rock reactions that can strongly influence migration of fluid and hydrocarbon through shale/fracture interfaces. Due to the extremely low permeability of shale matrixes, studies on chemical reactivity of shales have mostly focused on shale surfaces. Shale-fluid interactions inside within shale matrixes have not been examined, yet the matrix is the primary conduit through which hydrocarbons and potential contaminants are transmitted. To characterize changes in matrix mineralogy, porosity, diffusivity, and permeability during hydraulic stimulation, we reacted Marcellus (high clay and low carbonate) and Eagle Ford (low clay and high carbonate) shale cores with fracture fluids for 3 weeks at elevated pressure and temperature (80 oC, and 77 bars). In the carbonate-poor Marcellus system, fluid pH increased from 2 to 4, and secondary Fe(OH)3 precipitates were observed in the fluid. Sulfur X-ray fluorescence maps show that fluids had saturated and reacted with the entire 1-cm-diameter core. In the carbonate-rich Eagle Ford system, pH increased from 2 to 6 due to calcite dissolution. When additional Ba2+ and SO42- were present (log10(Q/K)=1.3), extensive barite precipitation was observed in the matrix of the Eagle Ford core (and on the surface). Barite precipitation was also observed on the surface of the Marcellus core, although to a lesser extent. In the Marcellus system, the presence of barite scale attenuated diffusivity in the matrix, as demonstrated by sharply reduced Fe leaching and much less sulfide oxidation. Systematic studies in homogeneous solution show that barite scale precipitation rates are highly sensitive to pH, salinity, and the presence of organic compounds. These findings imply that chemical reactions are not confined to shale/fluid interfaces but can penetrate into shale matrices, and that barite scale formation can clog diffusion pathways for both fluid and hydrocarbon.

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.

Pore-Scale Study of Transverse Mixing Induced CaCO ₃ Precipitation and Permeability Reduction in a Model Subsurface Sedimentary System

Energy Technology Data Exchange (ETDEWEB)

Zhang, Changyong; Dehoff, Karl; Hess, Nancy; Oostrom, Mart; Wietsma, Thomas W.; Valocchi, Albert J.; Fouke, Bruce W.; Werth, Charles J.

2010-10-15

A microfluidic pore structure etched into a silicon wafer was used as a two-dimensional model subsurface sedimentary system (i.e., a micromodel) to study mineral precipitation and permeability reduction relevant to groundwater remediation and geological carbon sequestration. Solutions containing CaCl₂ and Na₂CO₃ at four different saturation states (Ω = [Ca²⁺] [CO^32-] / KspCaCO₃) were introduced through two separate inlets and they mixed by diffusion transverse to the main flow direction along the center of the micromodel resulting in CaCO₃ precipitation. Precipitation rates increased and the total amount of precipitates decreased with increasing saturation state, and only vaterite and calcite crystals were formed (no aragonite). The relative amount of vaterite increased from 80% at the lowest saturation (Ω_v = 2.8 for vaterite) state to 95% at the highest saturation state (Ω_v = 4.5). Fluorescent tracer tests conducted before and after CaCO₃ precipitation indicate that pore spaces were completely occluded by CaCO₃ precipitates along the transverse mixing zone, thus significantly reducing porosity and permeability, and potentially limiting transformation from vaterite to the more stable calcite. The results suggest that mineral precipitation along plume margins can decrease both reactant mixing during groundwater remediation, and injection and storage efficiency during CO₂ sequestration.

228Ra and 226Ra measurement on a BaSO4 co-precipitation source

International Nuclear Information System (INIS)

Medley, Peter; Martin, Paul; Bollhöfer, Andreas; Parry, David

2015-01-01

One of the most commonly-used methods for determination of 226 Ra, particularly in water samples, utilises co-precipitation of Ra with BaSO 4 , followed by microfiltration to produce a source for alpha counting. This paper describes two extensions to BaSO 4 co-precipitation methods which enable determination of 228 Ra using the same source. The adaptations presented here do not introduce any contaminants that will affect the separation of radium or alpha counting for 226 Ra, and can be used for re-analysis of already existing sources prepared by BaSO 4 co-precipitation. The first adaptation uses detection of 228 Ac on the source by gamma spectrometry. The detection efficiency is high, allowing analysis of water samples at sufficiently low activity to be suitable in testing for compliance with drinking water quality standards. As 228 Ac grows in quickly, taking less than 2 days to reach equilibrium with the 228 Ra parent, this can also be useful in radiological emergency response situations. The second adaptation incorporates a method for the digestion of BaSO 4 sources, allowing separation of thorium and subsequent determination of 228 Th activity. Although ingrowth periods for 228 Th can be lengthy, very low detection limits for 228 Ra can be achieved with this technique. - Highlights: • We developed two methods for 228 Ra measurement on Ba(Ra)SO 4 co-precipitation sources. • Measurement by gamma spectrometry using the daughter 228 Ac is rapid. • Detection limits are suitable for assessment of drinking water quality. • The second approach uses alpha spectrometry on a separated Th fraction. • This is more sensitive than gamma spectrometry after an ingrowth period greater than about 1 month

Phosphor scintillator structure

International Nuclear Information System (INIS)

Cusano, D.A.; Prener, J.S.

1980-01-01

A method of fabricating scintillators is described in which the phosphor is distributed within the structure in such a way as to enhance the escape of the visible wavelength radiation that would otherwise be dissipated within the scintillator body. Two embodiments of the present invention are disclosed: one in which the phosphor is distributed in a layered structure and another in which the phosphor is dispersed throughout a transparent matrix. (U.K.)

Gas sensing properties of magnesium ferrite prepared by co-precipitation method

International Nuclear Information System (INIS)

Hankare, P.P.; Jadhav, S.D.; Sankpal, U.B.; Patil, R.P.; Sasikala, R.; Mulla, I.S.

2009-01-01

Polycrystalline magnesium ferrite (MgFe 2 O 4 ) was prepared by the co-precipitation method. The synthesized compound was characterized for their phase and morphology by X-ray diffraction and scanning electron microscopy, respectively. Conductance responses of the (MgFe 2 O 4 ) were measured towards gases like hydrogen sulfide (H 2 S), liquefied petroleum gas (LPG), ethanol vapors (C 2 H 5 OH), SO x , H 2 , NO x , NH 3, methanol, acetone and petrol. The gas sensing characterstics were obtained by measuring the sensitivity as a function of various controlling factors like operating temperatures and concentrations of gases. It was found that the sensor exhibited various responses towards these gases at different operating temperatures. Furthermore; the MgFe 2 O 4 based sensor exhibited a fast response and a good recovery towards petrol at temperature 250 deg. C. The results of the response towards petrol reveal that (MgFe 2 O 4 ) synthesized by a simple co-precipitation method, would be a suitable material for the fabrication of the petrol sensor.

High-temperature plastic flow of a precipitation-hardened FeCoNiCr high entropy alloy

Energy Technology Data Exchange (ETDEWEB)

He, J.Y.; Wang, H.; Wu, Y.; Liu, X.J. [State Key Laboratory for Advanced Metals and Materials, University of Science and Technology Beijing, Beijing 100083 (China); Nieh, T.G. [Department of Materials Science and Engineering, the University of Tennessee, Knoxville, TN 37996 (United States); Lu, Z.P., E-mail: luzhaoping@163.com [State Key Laboratory for Advanced Metals and Materials, University of Science and Technology Beijing, Beijing 100083 (China)

2017-02-16

In this work, we systematically investigated flow behavior of a high entropy alloy (HEA) strengthened by coherent γ′ precipitates in the temperature range of 1023–1173 K. In contrast to the single-phase FeCoNiCrMn HEA, this precipitate-hardened alloy, i.e., (FeCoNiCr){sub 94}Ti{sub 2}Al{sub 4}, exhibited large reduction of the steady-state strain rate (by ~2 orders of magnitude) or drastic enhancement in flow stress, indicating significant improvement in high-temperature properties. Our results showed that the deformation could be divided into two regimes. At temperatures below 1123 K, coherent γ′ precipitates effectively blocked the dislocation motion, thus resulted in a threshold stress effect. Above 1123 K, however, γ′ particles dissolved and the deformation was controlled by the ordinary dislocation climb mechanism. In addition, we conducted transmission electron microscopy to characterize dislocation-precipitate interaction to provide microstructural evidences to support our conclusion of the specific deformation mechanisms in the two temperature regimes.

Chemical and environmental isotopes study of precipitation in Syria

International Nuclear Information System (INIS)

Al-Charideh, A.; Abou Zakhem, B.

2009-02-01

Chemical and isotopic compositions of monthly precipitation were monitored at 12 stations distributed over the entire region in Syria for a period of 4 years from December 1999 to April 2003. Amount of precipitation and mean air temperature of rain monthly were also recorded. The conductivity of rain waters varies between 35 μ/cm in the mountainous stations and 336 μ/cm at Deir Az-Zor station. Excepted Tartous station, the mean value of Cl in the rainfall in all station is 3.8 mg/l. The seasonal variations in δ 18 O are smaller at west stations than to the east stations due to low seasonal temperature variations. All stations are characterized by water lines with slopes significantly lower than GMWL, except Bloudan, suggesting the influence of local factors on the isotopic composition of the precipitation. d-excess values decrease from 19% in the western part to 13% in the eastern part of Syria, indicating the influence of the precipitation generated by the air masses coming from the Mediterranean Sea over Syria. A reliable altitude effect represent by depletion of heavy stable isotopes of about -0.21, and -1.47, per 100 m elevation of 18 O and δ 2 H, respectively. Monthly tritium activity and seasonal variations pattern are low in the west stations than at the east stations. The weighted mean tritium values are between 3 to 9 TU during 2000-2003, and it is increasing with distance from the Syrian coast by 1 TU /100 Km. (author)

Water geochemistry of the Xijiang basin rivers, South China: Chemical weathering and CO2 consumption

International Nuclear Information System (INIS)

Xu Zhifang; Liu Congqiang

2010-01-01

Research highlights: → The Xijiang River is the second largest river in China and flows through a large carbonate rock region in South China. → Sulfuric acid, which emanate from acid precipitation and the oxidation of sulfide minerals, is involved as a proton donor in weathering reactions in the Xijiang basin. → Calculated results show that the contribution of cations from rock weathering induced by sulfuric acid accounts for approximately 11.2%. → The flux of CO 2 released into the atmosphere is approximately 0.41 x 10 12 gC yr -1 produced by sulfuric acid-induced carbonate weathering in the Xijiang basin. → Sulfuric acid-induced carbonate weathering could counterbalance a significant part of the CO 2 consumed by silicate weathering. - Abstract: The Xijiang River, the mainstream of the Zhujiang (Pearl) River, which is the second largest river in China in terms of discharge, flows through a large carbonate rock region in South China. The chemical and Sr isotopic compositions of the Xijiang waters were determined during the high-flow season in order to understand the chemical weathering processes, associated CO 2 consumption and anthropogenic influences within the carbonate-dominated basin. The major ion compositions of the river waters are characterized by the dominance of Ca 2+ , Mg 2+ , HCO 3 - and are significantly rich in SO 4 2- . The SO 4 2- is mainly derived from the oxidation of sulfide minerals and acid precipitation caused by coal combustion. Chemical and Sr isotopic compositions of the river waters indicate that four reservoirs (carbonates, silicates, evaporites and anthropogenic inputs) contribute to the total dissolved loads. The chemical weathering rates of carbonates and silicates for the Xijiang basin are estimated to be approximately 78.5 and 7.45 ton km -2 a -1 , respectively. The total chemical weathering rate of rocks for the Xijiang basin is approximately 86.1 ton km -2 a -1 or 42 mm ka -1 , which is much higher than global mean

Chemical Utilisation of CO

Indian Academy of Sciences (India)

Home; Journals; Resonance – Journal of Science Education; Volume 20; Issue 2. Chemical Utilisation of CO2: A Challenge for the Sustainable World. Dinesh Jagadeesan Bhaskar Joshi Prashant Parameswaran. General Article Volume 20 Issue 2 February 2015 pp 165-176 ...

Synthesis of Nano-Structured La0.6Sr0.4Co0.2Fe0.8O3 Perovskite by Co-Precipitation Method

Directory of Open Access Journals (Sweden)

Ebrahim Mostafavi

2015-06-01

Full Text Available Nano-structured lanthanum strontium cobalt ferrite, La0.6Sr0.4Co0.2Fe0.8O3 (LSCF, was successfully synthesized via co-precipitation method using metal nitrates as starting materials. Effects of precipitating agent and calcination temperature on the phase composition and morphology of synthesized powders were systematically studied using X-ray diffraction (XRD and field emission scanning electron microscopy (FESEM, respectively. XRD analysis revealed that a single phase La0.6Sr0.4Co0.2Fe0.8O3 perovskite was obtained in the processed sample using ammonium carbonate as precipitating agent with a NH4+/NO3-molar ratio of 2 after calcination at 1000C for 1 h. The phase composition of products was also affected by changing pH values. Moreover, using sodium hydroxide as a precipitant resulted in a mixture of La0.6Sr0.4Co0.2Fe0.8O3 and cobalt ferrite (CoFe2O4 phases. Careless washing of the precursors can also led to the formation of mixed phase after calcination of final powders. Mean crystallite size of the obtained powders was not noticeably affected by varying calcination temperature from 900 to 1050C and remained almost the same at 10 nm, however increasing calcination temperature to 1100C resulted in sharp structural coarsening. FESEM studies demonstrate that relatively uniform particles with mean particle size of 90 nm were obtained in the sample processed with a NH4+/NO3- molar ratio of 2 after calcination at 1000C for 1 h.

Enhanced Ce{sup 3+} photoluminescence by Li{sup +} co-doping in CaO phosphor and its use in blue-pumped white LEDs

Energy Technology Data Exchange (ETDEWEB)

Hao, Zhendong, E-mail: haozd@ciomp.ac.cn; Zhang, Xia; Luo, Yongshi; Zhang, Ligong; Zhao, Haifeng; Zhang, Jiahua, E-mail: zhangjh@ciomp.ac.cn

2013-08-15

In this paper, we demonstrate a method to improve the photoluminescence of CaO: Ce{sup 3+} phosphor and delineate its first use in blue-pumped white LEDs. The results show that the yellow emission of Ce{sup 3+} is enhanced by a factor of 1.88 by adding Li{sup +} into CaO host at 474 nm blue light excitation. On analyzing the diffuse reflection spectra and fluorescence decay curves, we reveal that the photoluminescence enhancement is originated from the rise of absorbance to the excitation photons but not from the improvement of the luminescent efficiency. Li{sup +}-improved CaO: Ce{sup 3+} exhibits more red component when it is compared with the commercial Y{sub 3}Al{sub 5}O{sub 12}: Ce{sup 3+} (YAG: Ce{sup 3+}) phosphor, indicating its potential application for high color rendering white LEDs. Thus, a white LED is fabricated by combining blue InGaN LED chip with CaO: Ce{sup 3+}, Li{sup +} phosphor and a warm white light with high color rendering index (R{sub a}) of 80, low correlated color temperature (T{sub c}) of 4524 K, and sufficient luminous efficiency of 50 lm W{sup −1} is obtained. -- Highlights: • The photoluminescence of Ce{sup 3+} in CaO host was enhanced by Li{sup +} co-doping. • A CaO: Ce{sup 3+}, Li{sup +} based white LED was fabricated for the first time. • An efficient warm white light was obtained. • CaO: Ce{sup 3+}, Li{sup +} is expected to be used as a yellow phosphor for blue-pumped white LEDs.

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.

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

Energy transfer in M₅(PO₄)₃  F:Eu²⁺,Ce³⁺ (M = Ca and Ba) phosphors.

Science.gov (United States)

Shinde, K N; Dhoble, S J

2014-08-01

M5(PO4)3F:Eu(2+) (M = Ca and Ba) co-doped with Ce(3+) phosphors were successfully prepared by the combustion synthesis method. The introduction of co-dopant (Ce(3+)) into the host enhanced the luminescent intensity of the M5(PO4)3F:Eu(2+) (M = Ca and Ba) efficiently. Previously, we have reported the synthesis and photoluminescence properties of same phosphors. The aim of this article is to report energy transfer mechanism between Ce(3+) ➔Eu(2+) ions in M5(PO4)3F:Eu(2+) (M = Ca and Ba) phosphors, where Ce(3+) ions act as sensitizers and Eu(2+) ions act as activators. The M5(PO4)3F:Eu(2+) (M = Ca and Ba) co-doped with Ce(3+) phosphor exhibits great potential for use in white ultraviolet (UV) light-emitting diode applications to serve as a single-phased phosphor that can be pumped with near-UV or UV light-emitting diodes. Copyright © 2013 John Wiley & Sons, Ltd.

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 highly sinterable YAG nanopowders by a modified co-precipitation method

International Nuclear Information System (INIS)

Chen, Zhi-Hui; Yang, Yun; Hu, Zhang-Gui; Li, Jiang-Tao; He, Shu-Li

2007-01-01

A hydrate precursor of yttrium aluminum garnet (YAG) was synthesized by a modified co-precipitation method, in which n-butanol was employed as a low-cost recyclable dehydration solvent. A mixed solution of ethanol and ammonia were used as precipitant. Pure YAG phase appeared after the as-prepared precursors being calcined at 850 o C for 2 h. The nanocrystalline YAG particles calcined at 1100 o C were well dispersed with average diameter of about 40 nm, which can be densified to transparency under vacuum sintering at 1700 o C for 5 h with TEOS as sintering additive

Gadolinium-doped ceria nanopowders synthesized by urea-based homogeneous co-precipitation (UBHP)

Energy Technology Data Exchange (ETDEWEB)

Accardo, G., E-mail: d16605@kist.re.kr [Fuel Cell Research Center, Korea Institute of Science and Technology, Hwarangno 14-gil, Seongbuk-gu, Seoul 136-791 (Korea, Republic of); Spiridigliozzi, L. [Department of Civil and Mechanical Engineering, INSTM Research Unit, University of Cassino and Southern Lazio, Via G. Di Biasio 43, 03043 Cassino, FR (Italy); Cioffi, R.; Ferone, C. [Department of Engineering, INSTM Research Unit, University Parthenope of Naples, Centro Direzionale, Is. C4, 80143 Napoli (Italy); Di Bartolomeo, E. [Department of Chemical Science and Technology, University of Rome “Tor Vergata”, Viale della Ricerca Scientifica, 00133 Rome (Italy); Yoon, Sung Pil [Fuel Cell Research Center, Korea Institute of Science and Technology, Hwarangno 14-gil, Seongbuk-gu, Seoul 136-791 (Korea, Republic of); Dell’Agli, G. [Department of Civil and Mechanical Engineering, INSTM Research Unit, University of Cassino and Southern Lazio, Via G. Di Biasio 43, 03043 Cassino, FR (Italy)

2017-02-01

Gadolinium (10%)-doped ceria was successfully synthesized by using an urea-based co-precipitation method (UBHP). A single fluorite phase was obtained after a low temperature (400 °C) calcination treatment. The resulting powders showed grains of nanometric size with some agglomerations and an overall good sinterability. Pellets were sintered at 1300 and 1500 °C for 3 h. The ionic conductivity was measured by electrochemical impedance spectroscopy measurements and a correlation between electrical properties and microstructure was revealed. The promising conductivity values showed that the synthesized powders are suitable for intermediate temperature solid oxide fuel cells (IT-SOFCs) applications. - Highlights: • Urea-based homogeneous co-precipitation is applied to synthesize nanocrystalline GDC. • Dense GDC samples at different sintering temperatures were characterized. • SEM and TEM revealed a well define microstructure and controlled composition. • Correlation between electrochemical properties by EIS and microstructure was discussed. • UBHP method can be used to prepare high performance GDC electrolytes.

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

Color-tunable and luminescence properties of phosphors of Ce{sup 3+} and Tb{sup 3+} co-doped La{sub 5}Si{sub 3}O{sub 12}N for UV w-LEDs

Energy Technology Data Exchange (ETDEWEB)

Deng, Junru; Chen, Jian; Liu, Yangai, E-mail: liuyang@cugb.edu.cn

2016-02-15

A series of Ce{sup 3+}, Tb{sup 3+} and Ce{sup 3+}/Tb{sup 3+} co-doped in La{sub 5}Si{sub 3}O{sub 12}N phosphors were synthesized by conventional high temperature solid state reaction method. With the increase of Tb{sup 3+}, the green emission was realized in (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y}){sub 5}Si{sub 3}O{sub 12}N phosphors on the basis of the efficient energy transfer from Ce{sup 3+} to Tb{sup 3+} with an efficiency (η{sub T}) over 58.72%. The room temperature PL decay curves of the Ce{sup 3+} ions in (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y}){sub 5}Si{sub 3}O{sub 12}N phosphors monitored at 460 nm with an excitation at 365 nm indicated that the energy transfer process between Ce{sup 3+} and Tb{sup 3+} indeed took place. The CIE chromaticity diagrams for (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y}){sub 5}Si{sub 3}O{sub 12}N phosphors were also observed, which shows the color tuned from blue to blue-greenish to green with the increase of Tb{sup 3+} concentration from 0.01 to 0.08. These results demonstrated that Tb{sup 3+} ion with low 4f–4f absorption efficiency in near UV region can play the role of an activator in narrow green-emitting phosphor through efficient energy feeding by allowing 4f–5d absorption of Ce{sup 3+} with high oscillator strength. All the results indicated that the Ce{sup 3+} and Tb{sup 3+} activated La{sub 5}Si{sub 3}O{sub 12}N phosphor may be good candidates for blue-green components in n-UV white LEDs. - Highlights: • A series of Ce{sup 3+}, Tb{sup 3+} and Ce{sup 3+}/Tb{sup 3+} co-doped in La{sub 5}Si{sub 3}O{sub 12}N phosphors were synthesized by high temperature solid state reaction method. • The green emission was realized in (La{sub 0.94−y}Ce{sub 0.06}Tb{sub y})Si{sub 3}O{sub 12}N phosphors on the basis of the highly efficient energy transfer. • The Ce{sup 3+} and Tb{sup 3+} activated La{sub 5}Si{sub 3}O{sub 12}N phosphor may be good candidates for blue-green components in n-UV white LEDs.

Revisiting Pocos de Caldas. Application of the co-precipitation approach to establish realistic solubility limits for performance assessment

International Nuclear Information System (INIS)

Bruno, J.; Duro, L.; Jordana, S.; Cera, E.

1996-02-01

Solubility limits constitute a critical parameter for the determination of the mobility of radionuclides in the near field and the geosphere, and consequently for the performance assessment of nuclear waste repositories. Mounting evidence from natural system studies indicate that trace elements, and consequently radionuclides, are associated to the dynamic cycling of major geochemical components. We have recently developed a thermodynamic approach to take into consideration the co-precipitation and co-dissolution processes that mainly control this linkage. The approach has been tested in various natural system studies with encouraging results. The Pocos de Caldas natural analogue was one of the sites where a full testing of our predictive geochemical modelling capabilities were done during the analogue project. We have revisited the Pocos de Caldas data and expanded the trace element solubility calculations by considering the documented trace metal/major ion interactions. This has been done by using the co-precipitation/co-dissolution approach. The outcome is as follows: A satisfactory modelling of the behaviour of U, Zn and REEs is achieved by assuming co-precipitation with ferrihydrite. Strontium concentrations are apparently controlled by its co-dissolution from Sr-rich fluorites. From the performance assessment point of view, the present work indicates that calculated solubility limits using the co-precipitation approach are in close agreement with the actual trace element concentrations. Furthermore, the calculated radionuclide concentrations are 2-4 orders of magnitude lower than conservative solubility limits calculated by assuming equilibrium with individual trace element phases. 34 refs, 18 figs, 13 tabs

Revisiting Pocos de Caldas. Application of the co-precipitation approach to establish realistic solubility limits for performance assessment

Energy Technology Data Exchange (ETDEWEB)

Bruno, J.; Duro, L.; Jordana, S.; Cera, E. [QuantiSci, Barcelona (Spain)

1996-02-01

Solubility limits constitute a critical parameter for the determination of the mobility of radionuclides in the near field and the geosphere, and consequently for the performance assessment of nuclear waste repositories. Mounting evidence from natural system studies indicate that trace elements, and consequently radionuclides, are associated to the dynamic cycling of major geochemical components. We have recently developed a thermodynamic approach to take into consideration the co-precipitation and co-dissolution processes that mainly control this linkage. The approach has been tested in various natural system studies with encouraging results. The Pocos de Caldas natural analogue was one of the sites where a full testing of our predictive geochemical modelling capabilities were done during the analogue project. We have revisited the Pocos de Caldas data and expanded the trace element solubility calculations by considering the documented trace metal/major ion interactions. This has been done by using the co-precipitation/co-dissolution approach. The outcome is as follows: A satisfactory modelling of the behaviour of U, Zn and REEs is achieved by assuming co-precipitation with ferrihydrite. Strontium concentrations are apparently controlled by its co-dissolution from Sr-rich fluorites. From the performance assessment point of view, the present work indicates that calculated solubility limits using the co-precipitation approach are in close agreement with the actual trace element concentrations. Furthermore, the calculated radionuclide concentrations are 2-4 orders of magnitude lower than conservative solubility limits calculated by assuming equilibrium with individual trace element phases. 34 refs, 18 figs, 13 tabs.

Magnetic and structural properties of Cu0.85Fe0.15O system synthesized by co-precipitation

International Nuclear Information System (INIS)

Colorado, H. D.; Pérez Alcázar, G. A.

2011-01-01

Cu 0.94 Fe 0.06 O and Cu 0.85 Fe 0.15 O samples were synthesized by using the co-precipitation chemical method. Starting from aqueous solutions of copper nitrate, CuO (NO 3 ) 2 3H 2 O, iron nitrate, Fe (NO 3 ) 3 9H 2 O and sodium hydroxide as precipitating agent, NaOH. The precipitate of three samples for Cu 0.94 Fe 0.06 O and five for Cu 0.85 Fe 0.15 O of fine powder were calcined for 5 h at different temperatures. The obtained X rays diffraction patterns refined by the Rietveld method show the CuO characteristic pattern, showing that the Fe atoms enter to replace Cu atoms. Furthermore, it was obtained that the crystallite size decreases with calcination temperatures for Cu 0.94 Fe 0.06 O. The transmission Mössbauer spectroscopy showed that the samples present a disordered paramagnetic behavior due to the big value of the half-width of line of the quadrupolar splitting. Vibrating sample magnetometry confirms the paramagnetic character. The XRD results indicate that the material is nanostructured, due that the crystallite sizes are of the order of 10 nm for Cu 0.94 Fe 0.06 O and 40 nm for Cu 0.85 Fe 0.15 O.

Hydromagnesite precipitation in the Alkaline Lake Dujiali, central Qinghai-Tibetan Plateau: Constraints on hydromagnesite precipitation from hydrochemistry and stable isotopes

International Nuclear Information System (INIS)

Lin, Yongjie; Zheng, Mianping; Ye, Chuanyong

2017-01-01

The mineral hydromagnesite, Mg 5 (CO 3 ) 4 (OH) 2 ·4H 2 O, is a common form of hydrated Mg-carbonate in alkaline lakes, yet the processes involved in its formation are not well understood. This study focuses on Dujiali Lake, in the central Qinghai-Tibetan Plateau (QTP), which is one of the few environments on the earth's surface with extensive Holocene precipitation of hydromagnesite. The hydrogeochemistry of surface waters, and the mineralogical, stable isotope (δ 13 C and δ 18 O), and radiogenic isotope content of hydromagnesite deposits were analyzed to investigate formation mechanisms. The chemical composition of surface water around Dujiali Lake evolved from the rock-weathering-type waters of T1 (Ca−Mg−HCO 3 water type) to more concentrated sodic waters of T2 (Na−SO 4 −Cl water type) due to evaporation. XRD results show that the mineralogical composition of samples is pure hydromagnesite. Analysis of oxygen isotopes in the hydromagnesite indicates that supergene formation with authigenic carbonate crystallization from evaporation water is the dominant precipitation process. Combined carbon-oxygen isotope analysis suggests atmospheric CO 2 provided a carbon source for the precipitation of hydromagnesite. These findings suggest that hydromagnesite precipitation at Lake Dujiali is mainly inorganic in nature, and the greenhouse gas, CO 2 , is trapped and stored in the hydromagnesite directly from the atmosphere. AMS radiocarbon dating of samples indicates CO 2 was sequestered between 5845 ± 30 to 6090 ± 25 cal a BP in the Dujiali Lake hydromagnesite deposit. The study contributes to improved understanding of hydromagnesite formation in modern and ancient playas. - Highlights: • The stable isotopes, radiogenic isotope data are firstly obtained from the hydromagnesite deposits of Lake Dujiali in QTP. • Hydromagnesite precipitation at Lake Dujiali is mainly inorganic. • δ 18 O indicates supergene formation with authigenic carbonate

Synthesis of aqueous suspensions of magnetic nanoparticles with the co-precipitation of iron ions in the presence of aspartic acid

Energy Technology Data Exchange (ETDEWEB)

Pušnik, Klementina; Goršak, Tanja [Department for Materials Synthesis, Jožef Stefan Institute, 1000 Ljubljana (Slovenia); Jožef Stefan International Postgraduate School, 1000 Ljubljana (Slovenia); Drofenik, Miha [Department for Materials Synthesis, Jožef Stefan Institute, 1000 Ljubljana (Slovenia); Faculty of Chemistry and Chemical Engineering, University of Maribor, 2000 Maribor (Slovenia); Makovec, Darko [Department for Materials Synthesis, Jožef Stefan Institute, 1000 Ljubljana (Slovenia); Jožef Stefan International Postgraduate School, 1000 Ljubljana (Slovenia)

2016-09-01

There is increasing demand for the production of large quantities of aqueous suspensions of magnetic iron-oxide nanoparticles. Amino acids are one possible type of inexpensive, nontoxic, and biocompatible molecules that can be used as the surfactants for the preparation of stable suspensions. This preparation can be conducted in a simple, one-step process based on the co-precipitation of Fe{sup 3+}/Fe{sup 2+} ions in the presence of the amino acid. However, the presence of this amino acid changes the mechanism of the magnetic nanoparticles' formation. In this investigation we analyzed the influence of aspartic amino acid (Asp) on the formation of magnetic iron-oxide nanoparticles during the co-precipitation. The process of the nanoparticles’ formation was followed using a combination of TEM, x-ray diffractometry, magnetic measurements, in-situ FT-IR spectroscopy, and chemical analysis, and compared with the formation of nanoparticles without the Asp. The Asp forms a coordination complex with the Fe{sup 3+} ions, which impedes the formation of the intermediate iron oxyhydroxide phase and suppresses the growth of the final magnetic iron-oxide nanoparticles. Slower reaction kinetics can lead to the formation of nonmagnetic secondary phases. The aspartic-acid-absorbed nanoparticles can be dispersed to form relatively concentrated aqueous suspensions displaying a good colloidal stability at an increased pH. - Highlights: • Co-precipitation of Fe{sup 3+}/Fe{sup 2+} ions in the presence of aspartic amino acid (Asp). • Through analysis of nanoparticle formation mechanism. • Presence of Asp changes the mechanism of the nanoparticles’ formation. • Asp forms a coordination complex with the Fe{sup 3+} ions. • Asp impedes the formation of iron oxyhydroxide phase and suppresses the growth of iron-oxide nanoparticles. • The aspartic-acid-absorbed nanoparticles form stable aqueous suspensions.

Synthesis of aqueous suspensions of magnetic nanoparticles with the co-precipitation of iron ions in the presence of aspartic acid

International Nuclear Information System (INIS)

Pušnik, Klementina; Goršak, Tanja; Drofenik, Miha; Makovec, Darko

2016-01-01

There is increasing demand for the production of large quantities of aqueous suspensions of magnetic iron-oxide nanoparticles. Amino acids are one possible type of inexpensive, nontoxic, and biocompatible molecules that can be used as the surfactants for the preparation of stable suspensions. This preparation can be conducted in a simple, one-step process based on the co-precipitation of Fe 3+ /Fe 2+ ions in the presence of the amino acid. However, the presence of this amino acid changes the mechanism of the magnetic nanoparticles' formation. In this investigation we analyzed the influence of aspartic amino acid (Asp) on the formation of magnetic iron-oxide nanoparticles during the co-precipitation. The process of the nanoparticles’ formation was followed using a combination of TEM, x-ray diffractometry, magnetic measurements, in-situ FT-IR spectroscopy, and chemical analysis, and compared with the formation of nanoparticles without the Asp. The Asp forms a coordination complex with the Fe 3+ ions, which impedes the formation of the intermediate iron oxyhydroxide phase and suppresses the growth of the final magnetic iron-oxide nanoparticles. Slower reaction kinetics can lead to the formation of nonmagnetic secondary phases. The aspartic-acid-absorbed nanoparticles can be dispersed to form relatively concentrated aqueous suspensions displaying a good colloidal stability at an increased pH. - Highlights: • Co-precipitation of Fe 3+ /Fe 2+ ions in the presence of aspartic amino acid (Asp). • Through analysis of nanoparticle formation mechanism. • Presence of Asp changes the mechanism of the nanoparticles’ formation. • Asp forms a coordination complex with the Fe 3+ ions. • Asp impedes the formation of iron oxyhydroxide phase and suppresses the growth of iron-oxide nanoparticles. • The aspartic-acid-absorbed nanoparticles form stable aqueous suspensions.

Amino acid salt solutions as solvents in CO2 capture from flue gas

DEFF Research Database (Denmark)

Lerche, Benedicte Mai; Thomsen, Kaj; Stenby, Erling Halfdan

New solvents based on the salts of amino acids have emerged as an alternative to the alkanolamine solutions, for the chemical absorption of CO2 from flue gas. But only few studies on amino acids as CO2 capturing agents have been performed so far. One of the interesting features of amino acid salt...... solutions is their ability to form solid precipitates upon the absorption of CO2. The occurrence of crystallization offers the possibility of increasing the CO2 loading capacity of the solvent. However, precipitation can also have negative effect on the CO2 capture process. The chemical nature of the solid...... of glycine, taurine, and lysine, while in the case of proline, and glutamic acid, the precipitate was found to be bicarbonate. These results give an important contribution to further understanding the potential of amino acid salt solutions in CO2 capture from flue gas....

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

High temperature thermometric phosphors

Science.gov (United States)

Allison, Stephen W.; Cates, Michael R.; Boatner, Lynn A.; Gillies, George T.

1999-03-23

A high temperature phosphor consists essentially of a material having the general formula LuPO.sub.4 :Dy.sub.(x),Eu.sub.y) wherein: 0.1 wt %.ltoreq.x.ltoreq.20 wt % and 0.1 wt %.ltoreq.y.ltoreq.20 wt %. The high temperature phosphor is in contact with an article whose temperature is to be determined. The article having the phosphor in contact with it is placed in the environment for which the temperature of the article is to be determined. The phosphor is excited by a laser causing the phosphor to fluoresce. The emission from the phosphor is optically focused into a beam-splitting mirror which separates the emission into two separate emissions, the emission caused by the dysprosium dopant and the emission caused by the europium dopent. The separated emissions are optically filtered and the intensities of the emission are detected and measured. The ratio of the intensity of each emission is determined and the temperature of the article is calculated from the ratio of the intensities of the separate emissions.

and aluminum-substituted cobalt ferrite prepared by co-precipitation ...

Indian Academy of Sciences (India)

Spinal ferrites having the general formula Co1-ZnFe2-AlO4 ( = 0.0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6) were prepared using the wet chemical co-operation technique. The samples were annealed at 800°C for 12 h and were studied by means of X-ray diffraction, magnetization and low field AC susceptibility measurements.

Synthesis of alumina/YAG 20 vol% composite by co-precipitation

Directory of Open Access Journals (Sweden)

Radosław Lach

2011-12-01

Full Text Available Co-precipitation of alumina/YAG precursor from aluminum and yttrium nitrate solution with ammonium carbonate results in dawsonite. Its crystallographic parameters differ from the compound precipitated with no yttrium additive. It suggests that yttrium ions become incorporated into the dawsonite structure. The DSC/TG and X-ray diffraction measurements show decomposition of dawsonite at elevated temperatures resulting in γ-Al2O3 and then δ- and θ-alumina modifications. Full transformation to α-Al2O3 and YAG occurs at temperatures higher than 1230°C. Starting powder for the sintering experiments was prepared using the coprecipitated precursor calcined at 600°C. Seeding of such powder with 5 wt.% α-Al2O3 results in material of 98% density at 1500°C. Much lower densification show compacts of unseeded powder.

The chemical evolution of a travertine-depositing stream: Geochemical processes and mass transfer reactions

Science.gov (United States)

Lorah, Michelle M.; Herman, Janet S.

1988-01-01

This field study focuses on quantitatively defining the chemical changes occurring in Falling Spring Creek, a travertine-depositing stream located in Alleghany County, Virginia. The processes of CO2outgassing and calcite precipitation or dissolution control the chemical evolution of the stream. The observed chemical composition of the water was used with the computerized geochemical model WATEQF to calculate aqueous speciation, saturation indices, and CO2 partial pressure values. Mass balance calculations were performed to obtain mass transfers of CO2 and calcite. Reaction times, estimated from stream discharge, were used with the mass transfer results to calculate rates of CO2, outgassing and calcite precipitation between consecutive sampling points. The stream, which is fed by a carbonate spring, is supersaturated with respect to CO2 along the entire 5.2-km flow path. Outgassing of CO2 drives the solution to high degrees of supersaturation with respect to calcite. Metabolic uptake of CO2 by photosynthetic plants is insignificant, because the high supply rate of dissolved carbon dioxide and the extreme agitation of the stream at waterfalls and rapids causes a much greater amount of inorganic CO2 outgassing to occur. Calcite precipitation is kinetically inhibited until near the crest of a 20-m vertical waterfall. Calcite precipitation rates then reach a maximum at the waterfall where greater water turbulence allows the most rapid escape of CO2. Physical evidence for calcite precipitation exists in the travertine deposits which are first observed immediately above the waterfall and extend for at least 1.0 km below the falls. Net calcite precipitation occurs at all times of the year but is greatest during low-flow conditions in the summer and early fall.

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.

Optimizing Available Phosphorus in Calcareous Soils Fertilized with Diammonium Phosphate and Phosphoric Acid Using Freundlich Adsorption Isotherm

Science.gov (United States)

Akhtar, Muhammad

2013-01-01

In calcareous soils, phosphorus (P) retention and immobilization take place due to precipitation and adsorption. Since soil pH is considered a major soil variable affecting the P sorption, an acidic P fertilizer could result in low P adsorption compared to alkaline one. Therefore, P adsorption from DAP and phosphoric acid (PA) required to produce desired soil solution P concentration was estimated using Freundlich sorption isotherms. Two soils from Faisalabad and T. T. Singh districts were spiked with 0, 10, and 20 % CaCO3 for 15 days. Freundlich adsorption isotherms (P = aC b/a) were constructed, and theoretical doses of PA and DAP to develop a desired soil solution P level (i.e., 0.20 mg L−1) were calculated. It was observed that P adsorption in soil increased with CaCO3. Moreover, at all the levels of CaCO3, P adsorption from PA was lower compared to that from DAP in both the soils. Consequently, lesser quantity of PA was required to produce desired solution P, 0.2 mg L−1, compared to DAP. However, extrapolating the developed relationship between soil CaCO3 contents and quantity of fertilizer to other similar textured soils needs confirmation. PMID:24307878

Influence of the synthesis route and parameters on the thermoluminescence response of ZnO phosphors

International Nuclear Information System (INIS)

Orante B, V.; Bernal, R.; Brown, F.; Castano, V.M.; Cruz V, C.

2007-01-01

Full text: ZnO nano phosphors obtained by thermal annealing of chemically synthesized ZnS powder has been recently reported to exhibit striking properties to be used as thermoluminescence (TL) dosimeters for intermediate and high doses of ionizing radiation. Encouraged by these results, we began a research focused to improve the process of fabrication of ZnO phosphors, by varying the chemical route and parameters of synthesis in each route. We essayed three different chemical ways to obtain ZnO. In each case, different sintering processes were applied to the product obtained from the chemical reaction. TL is very sensitive to impurities traces, whose incorporation is influenced by the synthesis history, so that we obtain that general features of TL glow curves can be tuned by controlling the synthesis parameters. (Author)

Co-precipitation of oppositely charged nanoparticles: the case of mixed ligand nanoparticles

International Nuclear Information System (INIS)

Moglianetti, Mauro; Ponomarev, Evgeniy; Szybowski, Maxime; Stellacci, Francesco; Reguera, Javier

2015-01-01

Colloid stability is of high importance in a multitude of fields ranging from food science to biotechnology. There is strong interest in studying the stability of small particles (of a size of a few nanometres) with complex surface structures, that make them resemble the complexity of proteins and other natural biomolecules, in the presence of oppositely charged nanoparticles. While for nanoparticles with homogeneously charged surfaces an abrupt precipitation has been observed at the neutrality of charges, data are missing about the stability of nanoparticles when they have more complex surface structures, like the presence of hydrophobic patches. To study the role of these hydrophobic patches in the stability of nanoparticles a series of negatively charged nanoparticles has been synthesized with different ratios of hydrophobic content and with control on the structural distribution of the hydrophobic moiety, and then titrated with positively charged nanoparticles. For nanoparticles with patchy nanodomains, the influence of hydrophobic content was observed together with the influence of the size of the nanoparticles. By contrast, for nanoparticles with a uniform distribution of hydrophobic ligands, size changes and hydrophobic content did not play any role in co-precipitation behaviour. A comparison of these two sets of nanoparticles suggests that nanodomains present at the surfaces of nanoparticles are playing an important role in stability against co-precipitation. (paper)

Characterization of metallic surfaces in phosphorous-bronze ordered packings

International Nuclear Information System (INIS)

Sandru, Claudia; Titescu, Gh.

1997-01-01

Copper and its alloys, particularly the phosphorous bronze, are characterized by a high water wettability as compared with other materials. This feature led to utilization of phosphorous bronze in fabrication of contact elements, a packing type equipping the distillation columns. For heavy water separation by isotopic distillation under vacuum, ordered packings of phosphorous bronze networks were fabricated. The superior performances of these packings are determined by the material and also by the geometrical form and the state of the metallic surface. Thus, a procedure of evaluating the wettability has been developed, based on tests of the network material. The results of the tests constitute a criterion of rating the functional performances of packings, particularly of their efficiencies. Also, investigation techniques of the chemical composition and of the thickness of superficial layer on the packing were developed. It was found that the packing surface presents a layer of about 5-20 μm formed mainly by oxides of copper, tin, and, depending on the packing treatment, of oxides of other elements coming from the treatment agent. The paper presents characterization of phosphorous bronze treated with potassium permanganate, a specific treatment for improving the functional performances of the packings used in the heavy water concentration and re-concentration installations

UV excited downconversion luminescence properties of Eu3+: NaZnPO4 phosphors

Science.gov (United States)

Mukhopadhyay, Lakshmi; Rai, Vineet Kumar

2018-05-01

The structural and optical properties of Eu3+: NaZnPO4 phosphors prepared by chemical coprecipitation method have been studied. The phase formation and morphology of the phosphors have been confirmed by the X-ray diffraction (XRD) and Field emission scanning electron microscopy (FESEM) analysis. The downconversion emission spectra upon 392 nm excitation exhibit five emission bands centred at ˜ 575 nm, ˜ 590 nm, ˜ 612 nm, ˜ 660 nm and ˜ 702 nm corresponding to the 5D0→7F0, 5D0→7F1, 5D0→7F2, 5D0→7F3 and 5D0→7F4 transitions of Eu3+ ions respectively. The observed downconversion emission peaks can be explained with the help of suitable energy level diagram. The CIE chromaticity diagram shows the purity of the emitted colour from the prepared phosphors. The present phosphors emit in intense red region which shows the applicability of the phosphors in red light emitting display devices.

Preparation and Characterization of UV Emitting Fluoride Phosphors for Phototherapy Lamps

Science.gov (United States)

Belsare, P. D.; Moharil, S. V.; Joshi, C. P.; Omanwar, S. K.

2011-10-01

The use of ultraviolet radiation for the treatment of various skin diseases is well known for long time. Phototherapy employs ultraviolet-blue radiation to cure skin diseases. The basis of phototherapy is believed to be the direct interaction of light of certain frequencies with tissue to cause a change in immune response. Currently dermatologists use UV lamps having specific emissions in UV region for treating various skin diseases. The treatment of skin diseases using artificial sources of UV radiation is now well established and more than 50 types of skin diseases are treated by phototherapy. This is an effective treatment for many skin disorders, such as psoriasis, vitiligo, ofujis disease, morphea , scleroderma, cutaneous T-cell lymphoma, lupus erythematosus, hyperbilirubinemia commonly known as infant jaundice, acne vulgaris, This paper reports photoluminescence properties of UV emitting fluoride phosphors prepared by wet chemical method. Emission characteristics of these phosphors are found similar to those of commercial UV lamp phosphors with comparable intensities. The usefulness of UV emitting fluoride phosphor is discussed in the paper.

Synthesis of aqueous suspensions of magnetic nanoparticles with the co-precipitation of iron ions in the presence of aspartic acid

Science.gov (United States)

Pušnik, Klementina; Goršak, Tanja; Drofenik, Miha; Makovec, Darko

2016-09-01

There is increasing demand for the production of large quantities of aqueous suspensions of magnetic iron-oxide nanoparticles. Amino acids are one possible type of inexpensive, nontoxic, and biocompatible molecules that can be used as the surfactants for the preparation of stable suspensions. This preparation can be conducted in a simple, one-step process based on the co-precipitation of Fe3+/Fe2+ ions in the presence of the amino acid. However, the presence of this amino acid changes the mechanism of the magnetic nanoparticles' formation. In this investigation we analyzed the influence of aspartic amino acid (Asp) on the formation of magnetic iron-oxide nanoparticles during the co-precipitation. The process of the nanoparticles' formation was followed using a combination of TEM, x-ray diffractometry, magnetic measurements, in-situ FT-IR spectroscopy, and chemical analysis, and compared with the formation of nanoparticles without the Asp. The Asp forms a coordination complex with the Fe3+ ions, which impedes the formation of the intermediate iron oxyhydroxide phase and suppresses the growth of the final magnetic iron-oxide nanoparticles. Slower reaction kinetics can lead to the formation of nonmagnetic secondary phases. The aspartic-acid-absorbed nanoparticles can be dispersed to form relatively concentrated aqueous suspensions displaying a good colloidal stability at an increased pH.

Conceptual design of a novel CO2 capture process based on precipitating amino acid solvents

NARCIS (Netherlands)

Sanchez Fernandez, E.; Heffernan, K.; Ham, L.V. van der; Linders, M.J.G.; Eggink, E.; Schrama, F.N.H.; Brilman, D.W.F.; Goetheer, E.L.V.; Vlugt, T.J.H.

2013-01-01

Amino acid salt based solvents can be used for CO2 removal from flue gas in a conventional absorption-thermal desorption process. Recently, new process concepts have been developed based on the precipitation of the amino acid zwitterion species during the absorption of CO2. In this work, a new

Bioelectrochemical conversion of CO2 to chemicals

NARCIS (Netherlands)

Bajracharya, Suman; Vanbroekhoven, Karolien; Buisman, Cees J.N.; Strik, David P.B.T.B.; Pant, Deepak

2017-01-01

The recent concept of microbial electrosynthesis (MES) has evolved as an electricity-driven production technology for chemicals from low-value carbon dioxide (CO2) using micro-organisms as biocatalysts. MES from CO2 comprises bioelectrochemical reduction of CO2 to multi-carbon organic compounds

Co-precipitation synthesis of YAG:Dy nanophosphor and its thermometric properties

International Nuclear Information System (INIS)

Chong, Joo-Yun; Zhang, Yuelan; Wagner, Brent K.; Kang, Zhitao

2013-01-01

Highlights: •YAG:Dy nanophosphors were synthesized with particle size of about 50 nm. •Optimized doping concentration of 6%Dy was determined. •Thermometric photoluminescence properties were studied between 20 and 350 °C. •Temperature-sensitive change in peak ratio of 496/457 nm emissions was demonstrated. •Suitable for potential thermographic applications when dispersed in a liquid media. -- Abstract: Dy 3+ doped yttrium aluminum garnet (YAG) nanophosphors were synthesized by a co-precipitation method for potential thermographic applications in a liquid media dispersed with fluorescent nanoparticles. The doping concentration and annealing temperature on the structural and optical properties of YAG:Dy were investigated. Pure phase YAG:Dy nanophosphors were obtained by annealing the co-precipitated hydroxide products at above 900 °C. Maximum photoluminescence intensity was observed from 6%Dy doped YAG samples. The effect of measuring temperature between 20 and 350 °C on the photoluminescence spectra of nano YAG:Dy was investigated. A temperature-sensitive change in the peak intensity ratio of 496/457 nm emission lines was demonstrated for such nanophosphors for the first time, suggesting potential applications in temperature monitoring of fuel spray

Co-precipitation synthesis of YAG:Dy nanophosphor and its thermometric properties

Energy Technology Data Exchange (ETDEWEB)

Chong, Joo-Yun [School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA 30332 (United States); Zhang, Yuelan [School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332 (United States); Wagner, Brent K. [Georgia Tech Research Institute, Georgia Institute of Technology, Atlanta, GA 30332 (United States); Kang, Zhitao, E-mail: zhitao.kang@gtri.gatech.edu [Georgia Tech Research Institute, Georgia Institute of Technology, Atlanta, GA 30332 (United States); School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, GA 30332 (United States)

2013-12-25

Highlights: •YAG:Dy nanophosphors were synthesized with particle size of about 50 nm. •Optimized doping concentration of 6%Dy was determined. •Thermometric photoluminescence properties were studied between 20 and 350 °C. •Temperature-sensitive change in peak ratio of 496/457 nm emissions was demonstrated. •Suitable for potential thermographic applications when dispersed in a liquid media. -- Abstract: Dy{sup 3+} doped yttrium aluminum garnet (YAG) nanophosphors were synthesized by a co-precipitation method for potential thermographic applications in a liquid media dispersed with fluorescent nanoparticles. The doping concentration and annealing temperature on the structural and optical properties of YAG:Dy were investigated. Pure phase YAG:Dy nanophosphors were obtained by annealing the co-precipitated hydroxide products at above 900 °C. Maximum photoluminescence intensity was observed from 6%Dy doped YAG samples. The effect of measuring temperature between 20 and 350 °C on the photoluminescence spectra of nano YAG:Dy was investigated. A temperature-sensitive change in the peak intensity ratio of 496/457 nm emission lines was demonstrated for such nanophosphors for the first time, suggesting potential applications in temperature monitoring of fuel spray.

Final Report: Development of a Chemical Model to Predict the Interactions between Supercritical CO2, Fluid and Rock in EGS Reservoirs

Energy Technology Data Exchange (ETDEWEB)

McPherson, Brian J. [University of Utah; Pan, Feng [University of Utah

2014-09-24

This report summarizes development of a coupled-process reservoir model for simulating enhanced geothermal systems (EGS) that utilize supercritical carbon dioxide as a working fluid. Specifically, the project team developed an advanced chemical kinetic model for evaluating important processes in EGS reservoirs, such as mineral precipitation and dissolution at elevated temperature and pressure, and for evaluating potential impacts on EGS surface facilities by related chemical processes. We assembled a new database for better-calibrated simulation of water/brine/ rock/CO2 interactions in EGS reservoirs. This database utilizes existing kinetic and other chemical data, and we updated those data to reflect corrections for elevated temperature and pressure conditions of EGS reservoirs.

The synthesis of hydroxyapatite through the precipitation method.

Science.gov (United States)

Shah, Rizal K; Fahmi, M N; Mat, Akil H; Zainal, Arifin A

2004-05-01

Hydroxyapatite (HA) has been earmarked as suitable for implantation within the human of its chemical makeup to human bone. In this paper, HA powders were synthesized via the precipitation method where phosphoric acid (H3PO4) was titrated into calcium hydroxide solution [Ca(OH)2]. Two parameters such as temperature and stirring rate were identified as factors that influenced the amount and purity of HA powder. Phase identification of the synthesized powder was done using X-Ray Diffraction (XRD). The results show that HA phase can be synthesized from this titration process of Ca(OH)2 and H3PO4 with yield amount of HA powder around 45 - 61 grams but with less than hundred percent purity. In order to study the effect of heat treatment to HA crystals structure, HA powder was calcined at 850 degrees C for 2 hours. It's found that the degree of crystallinity increases after calcination because of lattice expansion when the materials were heated at higher temperature

Taxa de emissão de CO2 de um latossolo fertirrigado com ácido fosfórico por gotejamento CO2 emission rate from a fertigated bare soil with phosphoric acid by dripping

Directory of Open Access Journals (Sweden)

José R. Zanini

2005-04-01

Full Text Available A aplicação de fertilizantes fosfatados por meio de fertirrigação com sistemas de irrigação localizada pode causar obstrução de emissores. Para evitar esse problema, pode ser utilizado o ácido fosfórico como fonte de fósforo às plantas. Porém, têm sido pouco investigados os efeitos da irrigação relacionados às perdas de CO2 do solo para a atmosfera, em conseqüência da decomposição do carbono orgânico e da infiltração de água no solo. Neste trabalho, investigou-se, no período de um mês, o efeito da fertirrigação com ácido fosfórico nas taxas de emissão de CO2 de um latossolo desprovido de vegetação, na Área Experimental de Irrigação da UNESP, Câmpus de Jaboticabal - SP. Utilizou-se de um sistema de irrigação por gotejamento, com delineamento experimental em blocos casualizados, constando de cinco repetições e cinco tratamentos (0; 30; 60; 90 e 120 kg ha-1de P2O5, aplicados via fertirrigação com ácido fosfórico. Verificou-se que as taxas de emissão de CO2 aumentaram significativamente após as fertirrigações, porém não houve efeito da dose do ácido fosfórico sobre as taxas. A umidade do solo mostrou-se um fator importante na relação entre as variações das taxas de emissão e a temperatura do solo ao longo do período estudado.The application of phosphoric fertilizers through fertigation, with localized irrigation systems, can cause emitters obstruction. In order to avoid this problem, the phosphoric acid can be used as phosphorus source to the plants. However, it has been little investigations on the effects of the irrigation practices, related to the CO2 transference to the atmosphere, due to organic matter decomposition in the soil and its water infiltration. At this work, the rates of emissions of CO2 from a bare soil without vegetation, and fertigated along one month were investigated. The experiment was conducted with randomized blocks design in São Paulo State University - UNESP

Chemical characteristics, deposition fluxes and source apportionment of precipitation components in the Jiaozhou Bay, North China

Science.gov (United States)

Xing, Jianwei; Song, Jinming; Yuan, Huamao; Li, Xuegang; Li, Ning; Duan, Liqin; Qu, Baoxiao; Wang, Qidong; Kang, Xuming

2017-07-01

To systematically illustrate the chemical characteristics, deposition fluxes and potential sources of the major components in precipitation, 49 rainwater and snow water samples were collected in the Jiaozhou Bay from June 2015 to May 2016. We determined the pH, electric conductivity (EC) and the concentrations of main ions (Na+, K+, Ca2 +, Mg2 +, NH4+, SO42 -, NO3-, Cl- and F-) as well as analyzed their source contributions and atmospheric transport. The results showed that the precipitation samples were severely acidified with an annual volume-weighted mean (VWM) pH of 4.77. The frequency of acid precipitation (pH pollution level over the Jiaozhou Bay. Surprisingly, NH4+ (40.4%), which is higher than Ca2 + (29.3%), is the dominant species of cations, which is different from that in most areas of China. SO42 - was the most abundant anions, and accounted for 41.6% of the total anions. The wet deposition fluxes of sulfur (S) was 12.98 kg ha- 1 yr- 1. Rainfall, emission intensity and long-range transport of natural and anthropogenic pollutants together control the concentrations and wet deposition fluxes of chemical components in the precipitation. Non-sea-salt SO42 - and NO3- were the primary acid components while NH4+ and non-sea-salt Ca2 + were the dominating neutralizing constituents. The comparatively lower rainwater concentration of Ca2 + in the Jiaozhou Bay than that in other regions in Northern China likely to be a cause for the strong acidity of precipitation. Based on the combined enrichment factor and correlation analysis, the integrated contributions of sea-salt, crustal and anthropogenic sources to the total ions of precipitation were estimated to be 28.7%, 14.5% and 56.8%, respectively. However, the marine source fraction of SO42 - may be underestimated as the contribution from marine phytoplankton was neglected. Therefore, the precipitation components in the Jiaozhou Bay present complex chemical characteristics under the combined effects of natural

Hydrothermal synthesis and tunable luminescent properties of Sr{sub 2-x}Dy {sub x}CeO{sub 4} rod-like phosphors derived from co-precipitation precursors

Energy Technology Data Exchange (ETDEWEB)

He Xianghong [School of Chemistry and Chemical Engineering, Jiangsu Teachers' University of Technology, Changzhou, Jiangsu 213001 (China) and Jiangsu Province Key Laboratory of Precious Metal Chemistry and Technology, Changzhou, Jiangsu 213001 (China)]. E-mail: hexh@jstu.edu.cn; Li Weihua [School of Chemistry and Chemical Engineering, Jiangsu Teachers' University of Technology, Changzhou, Jiangsu 213001 (China); Jiangsu Province Key Laboratory of Precious Metal Chemistry and Technology, Changzhou, Jiangsu 213001 (China); Zhou Quanfa [School of Chemistry and Chemical Engineering, Jiangsu Teachers' University of Technology, Changzhou, Jiangsu 213001 (China); Jiangsu Province Key Laboratory of Precious Metal Chemistry and Technology, Changzhou, Jiangsu 213001 (China)

2006-09-25

Uniform rod-like Sr{sub 2-x}Dy {sub x}CeO{sub 4} nano-phosphors with orthorhombic structure were prepared via a hydrothermal method, in the absence of any surfactant or template. The structure, morphology, particle size, and tunable luminescence properties of the samples were investigated by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SAED), UV-vis absorption and photoluminescence spectrum, respectively. The as-prepared phase-pure Sr{sub 2-x}Dy {sub x}CeO{sub 4} nanorods had the length of 50-150 nm and width of 80 nm. The Dy{sup 3+} ions emission in Sr{sub 2-x}Dy {sub x}CeO{sub 4} could be effectively excited through the energy absorbed by Sr{sub 2}CeO{sub 4} host. The tunable photoluminescence has been observed from Sr{sub 2}CeO{sub 4} doped with Dy{sup 3+} ions. Emission color of Sr{sub 2-x}Dy {sub x}CeO{sub 4} phosphor could be regulated from blue-white to white to yellow by adjusting the Dy{sup 3+} doping content in Sr{sub 2}CeO{sub 4} host, which originated from energy transfer between two different emission centers.

Precipitates/Salts Model Sensitivity Calculation

Energy Technology Data Exchange (ETDEWEB)

P. Mariner

2001-12-20

The objective and scope of this calculation is to assist Performance Assessment Operations and the Engineered Barrier System (EBS) Department in modeling the geochemical effects of evaporation on potential seepage waters within a potential repository drift. This work is developed and documented using procedure AP-3.12Q, ''Calculations'', in support of ''Technical Work Plan For Engineered Barrier System Department Modeling and Testing FY 02 Work Activities'' (BSC 2001a). The specific objective of this calculation is to examine the sensitivity and uncertainties of the Precipitates/Salts model. The Precipitates/Salts model is documented in an Analysis/Model Report (AMR), ''In-Drift Precipitates/Salts Analysis'' (BSC 2001b). The calculation in the current document examines the effects of starting water composition, mineral suppressions, and the fugacity of carbon dioxide (CO{sub 2}) on the chemical evolution of water in the drift.

Chemical treatment and biomimetic coating evaluating in zirconia-alumina ceramics

International Nuclear Information System (INIS)

Aguiar, Amanda Abati

2007-01-01

Ceramic materials, as alumina and zirconia have been explored along the years as biomaterials application. The bio inert nature has been stimulating the development of new alternatives, as chemical treatments to improve the biological application of these ceramics. The biomimetic process of bio inert ceramics for coating apatite is based on soaking the implant in a simulated body fluid, SBF, with ion concentrations nearly equal to those of human blood plasma. The bioactivity of the material is related with the formation of a layer constituted of hydroxyapatite low crystalline, similar to the biological apatite. The biocompatibility associated to the structural properties of the alumina and zirconia has been stimulating the clinical use of these materials, mainly in areas of larger mechanical requests, places not recommended for bioactive hydroxyapatite, for instance. In this work samples of alumina, zirconia doped with Yttria (3% mol) and composites of alumina and zirconia doped with Yttria (3% mol) were prepared by co-precipitation method, calcinate, sintered, chemically treated with solutions of acid phosphoric and sodium hydroxide and them immersed in 1.0 M and 1.5 M SBF. The calcinate powders were analyzed by X-ray diffraction (XRD), scanning electron microscopy (SEM), gas adsorption (BET) and laser diffraction. The XRD results indicate that the samples are low crystalline. It was observed for BET that the samples present high specific surface area. The results of laser diffraction and SEM showed that the powders are agglomerates. The sintered samples were analyzed by XRD, SEM and X-ray fluorescence (XRF). The phases quantified by Rietveld method were: cubic, tetragonal and monoclinic of the zirconia, besides the phase alpha of the alumina. The chemical treatment with phosphoric acid didn't present a tendency of larger apatite formation in relation to the samples no chemically treated. The treatment with sodium hydroxide provoked accentuated transformation of

Suitability of Sr{sub 0.5}Ba{sub 0.5-x}Ce{sub x}Fe{sub 12-y}Ni{sub y}O{sub 19} co-precipitated nanomaterials for inductor applications

Energy Technology Data Exchange (ETDEWEB)

Iqbal, Muhammad Javed, E-mail: mjiqauchem@yahoo.co [Surface and Solid State Chemistry Laboratory, Department of Chemistry, Quaid-i-Azam University, Islamabad 45320 (Pakistan); Farooq, Saima [Surface and Solid State Chemistry Laboratory, Department of Chemistry, Quaid-i-Azam University, Islamabad 45320 (Pakistan)

2010-03-18

The present investigation deals with the synthesis and characterization of Ce-Ni ions substituted nanocrystalline strontium-barium hexaferrites (Sr{sub 0.5}Ba{sub 0.5}Fe{sub 12}O{sub 19}) by the chemical co-precipitation method, with focus on the optimization of annealing temperature for the hexagonal phase development. The synthesis involves co-precipitation of aqueous solutions of water-soluble salts of strontium, barium and iron, at pH 9 using an ammonium hydroxide solution as a precipitating agent. The optimum temperature of annealing, necessary for the hexagonal phase development, is determined on the basis of thermo-gravimetric analysis (TGA). The co-precipitate is annealed at a temperature of 1323 K for 6 h, to produce a single magnetoplumbite phase of Sr-Ba hexaferrites, with the corresponding average crystallite size ranging from 36 to 48 nm. Observed changes in the lattice structure determined by the powder X-ray diffraction (XRD) studies are not in contradiction with the results of TGA. DC-electrical resistivity increases from 1.8 x 10{sup 10} to 12.5 x 10{sup 10} {Omega} cm, whereas the drift mobility, dielectric constant and dielectric loss tangent decrease with increasing the Ce-Ni content of the samples. Material of above-mentioned characteristics is considered to be suitable for applications in the microwave and surface mount devices (SMD) for fabricating the multilayer chip inductors (MLCI).

Stoichiometric hydroxyapatite obtained by precipitation and sol gel processes

Energy Technology Data Exchange (ETDEWEB)

Guzman V, C.; Pina B, C.; Munguia, N. [IIM-UNAM, A.P. 70-360, 04510 Mexico D.F. (Mexico)]. e-mail: caroguz@servidor.unam.mx

2005-07-01

Three methods for obtaining hydroxyapatite (HA) are described. HA is a very interesting ceramic because of its many medical applications. The first two precipitation methods start from calcium and phosphorous compounds, whereas the third method is a sol-gel process that uses alkoxides. The products were characterized and compared. The observed differences are important for practical applications. (Author)

Facile Synthesis and Characterization of ZrO₂ Nanoparticles via Modified Co-Precipitation Method.

Science.gov (United States)

Ramachandran, M; Subadevi, R; Liu, Wei-Ren; Sivakumar, M

2018-01-01

The crystalline Zirconium oxide (ZrO2) nano particles were synthesized using optimized content of Zirconium nitrate (Zr(NO3)2·3H2O) with varying KOH concentration (0.5, 1 and 1.5 M) by co-precipitation method. The thermal history of the precursor was carefully analyzed through Thermogravimetric (TG/DTA) measurement. The as prepared samples were characterized to ensure structural, functional, morphological, compositional, chemical composition and band gap by X-ray diffractometer (XRD), Fourier transform infrared spectroscopy (FTIR), Laser Raman, scanning electron microscopy (SEM), High resolution Transverse Electron Microscopy (HR-TEM), X-ray photo electron spectroscopy (XPS), EDX, Photo luminescence spectroscopy (PL). The monoclinic structure with space group P21/c has been confirmed from XRD (JCPDS 89-9066). The Zr-O stretching vibration and Zr-O2-Zr bending vibrations were confirmed through FTIR analysis. The well dispersed particles with spherical morphology were confirmed through SEM and TEM analysis. The oxidation states of Zr, O and C were confirmed through XPS analysis. The oxygen vacancies and band gap of the particles were investigated through PL analysis.

Effect of Calcination at Synthesis of Mg-Al Hydrotalcite Using co-Precipitation Method

Directory of Open Access Journals (Sweden)

Niar Kurnia Julianti

2017-01-01

Full Text Available The use of hydrotalcite in catalysis has wide attention in academic research and industrial parties. Based on its utilization, hydrotalcite can be active catalyst or support. This research is focused on the investigation of characteristic like spesific surface area of Mg-Al hydrotalcite which is prepared with different temperature of calcination. Synthesis of Mg-Al hydrotalcites with Mg/Al molar ratio 3:1 were prepared by co-precipitation method. Mg(NO33.6H2O and Al(NO33.9H2O as precursors of Mg-Al hydrotalcite. Na2CO3 was used as precipitant agent and NaOH was used as buffer solution. The solution was mixed and aging for 5 hours at 650oC. The dried precipitate was calcined at 2500oC, 3500oC, 4500oC, 5500oC and 6500oC. The characterization of functional group was determined by Fourier Transform Infra Red (FT-IR. The Identical peaks diffractogram were analyzed by X-Ray Diffraction (XRD. The spesific surface area was determined by adsorption-desorption of nitrogen. The largest surface area that obtained from the calcination temperature of 650oC is 156.252 m2/g.

Liberation of Adsorbed and Co-Precipitated Arsenic from Jarosite, Schwertmannite, Ferrihydrite, and Goethite in Seawater

Directory of Open Access Journals (Sweden)

Rodrigo Alarcón

2014-07-01

Full Text Available Sea level rise is able to change the geochemical conditions in coastal systems. In these environments, transport of contaminants can be controlled by the stability and adsorption capacity of iron oxides. The behavior of adsorbed and co-precipitated arsenic in jarosite, schwertmannite, ferrihydrite, and goethite in sea water (common secondary minerals in coastal tailings was investigated. The aim of the investigation was to establish As retention and transport under a marine flood scenario, which may occur due to climate change. Natural and synthetic minerals with co-precipitated and adsorbed As were contacted with seawater for 25 days. During this period As, Fe, Cl, SO4, and pH levels were constantly measured. The larger retention capability of samples with co-precipitated As, in relation with adsorbed As samples, reflects the different kinetics between diffusion, dissolution, and surface exchange processes. Ferrihydrite and schwertmannite showed good results in retaining arsenic, although schwertmannite holding capacity was enhanced due its buffering capacity, which prevented reductive dissolution throughout the experiment. Arsenic desorption from goethite could be understood in terms of ion exchange between oxides and electrolytes, due to the charge difference generated by a low point-of-zero-charge and the change in stability of surface complexes between synthesis conditions and natural media.

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

Mechanisms of Se(IV) Co-precipitation with Ferrihydrite at Acidic and Alkaline Conditions and Its Behavior during Aging

DEFF Research Database (Denmark)

Francisco, Paul Clarence M.; Sato, Tsutomu; Otake, Tsubasa

2018-01-01

in nanopore and defect structures. These results demonstrate a potential long-term immobilization pathway for Se(IV) even after phase transformation. This work presents one of the first direct insights on Se(IV) co-precipitation and its behavior in response to iron phase transformations.......Understanding the form of Se(IV) co-precipitated with ferrihydrite and its subsequent behavior during phase transformation is critical to predicting its long-term fate in a range of natural and engineered settings. In this work, Se(IV)-ferrihydrite co-precipitates formed at different pH were......, Se(IV) was removed dominantly as a ferric selenite-like phase intimately associated with ferrihydrite, while at pH 10, it was mostly present as a surface species on ferrihydrite. Similarly, the behavior of Se(IV) and the extent of its retention during phase transformation varied with pH. At pH 5, Se...

Synthesis of Lead Sulfide Nanoparticles by Chemical Precipitation Method

International Nuclear Information System (INIS)

Chongad, L S; Sharma, A; Banerjee, M; Jain, A

2016-01-01

Lead sulfide (PbS) nanoparticles were prepared by chemical precipitation method (CPM) with the assistance of H 2 S gas. The microstructure and morphology of the synthesized nanoparticles have been investigated using X-ray diffraction (XRD) and transmission electron microscopy (TEM). The XRD patterns of the PbS nanoparticles reveal formation of cubic phase. To investigate the quality of prepared nanoparticles, the particles size, lattice constant, strain, dislocation density etc. have been determined using XRD. TEM images reveal formation of cubic nanoparticles and the particle size determined from TEM images agree well with those from XRD. (paper)

Effect of Co2+ Ions Doping on the Structural and Optical Properties of Magnesium Aluminate

Science.gov (United States)

Kanwal, Kiran; Ismail, Bushra; Rajani, K. S.; Kissinger, N. J. Suthan; Zeb, Aurang

2017-07-01

Cobalt-doped nanosized magnesium aluminate (Mg1-xCoxAl2O4) samples having different compositions ( x = 0.2, 0.4, 0.6, 0.8, 1.0) were synthesized by a chemical co-precipitation method. All samples were characterized by means of x-ray diffraction (XRD), scanning electron microscopy, Fourier transform infrared spectroscopy, ultra violet-visible spectroscopy, photoluminescence and diffused reflectance spectroscopy. The results of XRD revealed that the samples were spinel single phase cubic close packed crystalline materials. The lattice constant and x-ray density were found to be affected by the ionic radii of the doped metal cations. Using the Debye-Scherrer formula, the calculated crystalline size was found to be Co2+ ion concentration-dependent and varied between 32 nm and 40 nm. Nano-dimensions and phase of the Mg1-xCoxAl2O4 samples were analyzed and the replacement of Mg2+ ions with Co2+ ions was confirmed by elemental analysis. Three strong absorption bands at 540 nm, 580 nm and 630 nm were observed for the doped samples which are attributed to the three spin-allowed 4T1g (4F) → 4T2g, 4A2g, 4T1g (4P) electronic transitions of Co2+ at tetrahedral lattice sites. Nanophosphors have optical properties different from bulk because of spatial confinement and non-radiative relaxation. Decreases in particle size can increase the surface area and the defects, which can in turn increase the luminescent efficiency to make it very useful for tunable laser operations, persistent phosphorescence, color centers, photoconductivity and luminescence for display technology. MgAl2O4 was doped with Co2+ ions using a co-precipitation method and the optical absorption studies revealed that there is a decrease of band gap due to the increase of Co2+ content. The emission intensity of this phosphor is observed at 449 nm with a sharp peak attributed to the smaller size of the particles and the homogeneity of the powder.

Synthesis of layered double hydroxides containing Mg2+, Zn2+, Ca2+ and Al3+ layer cations by co-precipitation methods-A review

Science.gov (United States)

Theiss, Frederick L.; Ayoko, Godwin A.; Frost, Ray L.

2016-10-01

Co-precipitation is a common method for the preparation of layered double hydroxides (LDHs) and related materials. This review article is aimed at providing newcomers to the field with some examples of the types of co-precipitation reactions that have been reported previously and to briefly investigate some of the properties of the products of these reactions. Due to the sheer volume of literature on the subject, the authors have had to limit this article to the synthesis of Mg/Al, Zn/Al and Ca/Al LDHs by co-precipitation and directly related methods. LDHs have been synthesised from various reagents including metal salts, oxides and hydroxides. Co-precipitation is also useful for the direct synthesis of LDHs with a wide range of interlayer anions and various bases have been successfully employed to prepare LDHs. Examples of other synthesis techniques including the urea method, hydrothermal synthesis and various mechanochemical methods that are undoubtedly related to co-precipitation have also been included in this review. The effect of post synthesis hydrothermal has also been summarised.

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.

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

International Nuclear Information System (INIS)

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

1976-01-01

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

Simultaneous nitrogen, phosphorous, and hardness removal from reverse osmosis concentrate by microalgae cultivation.

Science.gov (United States)

Wang, Xiao-Xiong; Wu, Yin-Hu; Zhang, Tian-Yuan; Xu, Xue-Qiao; Dao, Guo-Hua; Hu, Hong-Ying

2016-05-01

While reverse osmosis (RO) is a promising technology for wastewater reclamation, RO concentrate (ROC) treatment and disposal are important issues to consider. Conventional chemical and physical treatment methods for ROC present certain limitations, such as relatively low nitrogen and phosphorus removal efficiencies as well as the requirement of an extra process for hardness removal. This study proposes a novel biological approach for simultaneous removal of nitrogen, phosphorus, and calcium (Ca(2+)) and magnesium (Mg(2+)) ions from the ROC of municipal wastewater treatment plants by microalgal cultivation and algal biomass production. Two microalgae strains, Chlorella sp. ZTY4 and Scenedesmus sp. LX1, were used for batch cultivation of 14-16 days. Both strains grew well in ROC with average biomass production of 318.7 mg/L and lipid contents up to 30.6%, and nitrogen and phosphorus could be effectively removed with efficiencies of up to 89.8% and 92.7%, respectively. Approximately 55.9%-83.7% Ca(2+) could be removed from the system using the cultured strains. Mg(2+) removal began when Ca(2+) precipitation ceased, and the removal efficiency of the ion could reach up to 56.0%. The most decisive factor influencing Ca(2+) and Mg(2+) removal was chemical precipitation with increases in pH caused by algal growth. The results of this study provide a new biological approach for removing nitrogen, phosphorous, and hardness from ROC. The results suggest that microalgal cultivation presents new opportunities for applying an algal process to ROC treatment. The proposed approach serves dual purposes of nutrient and hardness reduction and production of lipid rich micro-algal biomass. Copyright © 2016 Elsevier Ltd. All rights reserved.

Treatment of low and intermediate aqueous waste containing Cs-137 by chemical precipitation

International Nuclear Information System (INIS)

Valdezco, E.M.; Marcelo, E.A.; Alamares, A.L.; Junio, J.B.; Dela Cruz, J.M.

1996-01-01

The use of radioactive materials in various applications has been increasing since its introduction in the early sixties. The Philippine Nuclear Research Institute has established a centralized facility for treating radioactive wastes i.e. aqueous wastes with assistance from the International Atomic Energy Agency - Technical Cooperation Programme. Liquid wastes containing Cs-137 are generated from aqueous wastes containing Cs-137 by nickel ferrocyanide precipitation will be presented. The aim of this study is to investigate the efficiency treatment in removing Cs-137 from an aqueous effluent. Actual aqueous wastes known to contain Cs-137 were used in the experiments. Low cost and simple nickel ferrocyanide precipitation method with the aid of a flocculant has been selected for the separation of Cs-137 from low and intermediate aqueous waste. By varying the chemical dosage added into the aqueous waste, different decontamination factors were obtained. Hence, the optimum dosage of the chemicals that give the highest decontamination factor can be determined. (author)

A review and evaluation of forest canopy epiphyte roles in the partitioning and chemical alteration of precipitation

Energy Technology Data Exchange (ETDEWEB)

Van Stan, John T., E-mail: jvanstan@georgiasouthern.edu [Dept. of Geology and Geography, Georgia Southern University, Statesboro, GA 30460 (United States); Pypker, Thomas G. [Dept. of Natural Resource Sciences, Thompson Rivers University, Kamloops, BC (Canada)

2015-12-01

Interactions between precipitation and forest canopy elements (bark, leaves, and epiphytes) control the quantity, spatiotemporal patterning, and the chemical concentration, character and constituency of precipitation to soils. Canopy epiphytes exert a range of hydrological and biogeochemical effects due to their diversity of morphological traits and nutrient acquisition mechanisms. We reviewed and evaluated the state of knowledge regarding epiphyte interactions with precipitation partitioning (into interception loss, throughfall, and stemflow) and the chemical alteration of net precipitation fluxes (throughfall and stemflow). As epiphyte species are quite diverse, this review categorized findings by common paraphyletic groups: lichens, bryophytes, and vascular epiphytes. Of these groups, vascular epiphytes have received the least attention and lichens the most. In general, epiphytes decrease throughfall and stemflow and increase interception loss. Epiphytes alter the spatiotemporal pattern of throughfall and increase overall latent heat fluxes from the canopy. Epiphytes alter biogeochemical processes by impacting the transfer of solutes through the canopy; however, the change in solute concentration varies with epiphyte type and chemical species. We discuss several important knowledge gaps across all epiphyte groups. We also explore innovative methods that currently exist to confront these knowledge gaps and past techniques applied to gain our current understanding. Future research addressing the listed deficiencies will improve our knowledge of epiphyte roles in water and biogeochemical processes coupled within forest canopies—processes crucial to supporting microbe, plant, vertebrate and invertebrate communities within individual epiphytes, epiphyte assemblages, host trees, and even the forest ecosystem as a whole. - Highlights: • Reviews > 100 studies on epiphyte effects on throughfall, stemflow, & interception • Identifies shared hydro

A review and evaluation of forest canopy epiphyte roles in the partitioning and chemical alteration of precipitation

International Nuclear Information System (INIS)

Van Stan, John T.; Pypker, Thomas G.

2015-01-01

Interactions between precipitation and forest canopy elements (bark, leaves, and epiphytes) control the quantity, spatiotemporal patterning, and the chemical concentration, character and constituency of precipitation to soils. Canopy epiphytes exert a range of hydrological and biogeochemical effects due to their diversity of morphological traits and nutrient acquisition mechanisms. We reviewed and evaluated the state of knowledge regarding epiphyte interactions with precipitation partitioning (into interception loss, throughfall, and stemflow) and the chemical alteration of net precipitation fluxes (throughfall and stemflow). As epiphyte species are quite diverse, this review categorized findings by common paraphyletic groups: lichens, bryophytes, and vascular epiphytes. Of these groups, vascular epiphytes have received the least attention and lichens the most. In general, epiphytes decrease throughfall and stemflow and increase interception loss. Epiphytes alter the spatiotemporal pattern of throughfall and increase overall latent heat fluxes from the canopy. Epiphytes alter biogeochemical processes by impacting the transfer of solutes through the canopy; however, the change in solute concentration varies with epiphyte type and chemical species. We discuss several important knowledge gaps across all epiphyte groups. We also explore innovative methods that currently exist to confront these knowledge gaps and past techniques applied to gain our current understanding. Future research addressing the listed deficiencies will improve our knowledge of epiphyte roles in water and biogeochemical processes coupled within forest canopies—processes crucial to supporting microbe, plant, vertebrate and invertebrate communities within individual epiphytes, epiphyte assemblages, host trees, and even the forest ecosystem as a whole. - Highlights: • Reviews > 100 studies on epiphyte effects on throughfall, stemflow, & interception • Identifies shared hydro

Investigation of Upconversion, downshifting and quantum –cutting behavior of Eu3+, Yb3+, Bi3+ co-doped LaNbO4 phosphor as a spectral conversion material

Science.gov (United States)

Dwivedi, A.; Mishra, K.; Rai, S. B.

2018-06-01

This work presents the spectral conversion characteristics [upconversion (UC), downshifting (DS) and quantum–cutting (QC) optical processes] of Eu3+, Yb3+ and Bi3+ co-doped LaNbO4 (LBO) phosphor samples synthesized by solid state reaction technique. The crystal structure and the pure phase formation have been confirmed by x-ray diffraction (XRD) measurements. The surface morphology and particle size are studied by scanning electron microscopy (SEM). The rarely observed intense red UC emission from Eu3+ ion has been successfully obtained in Eu3+/Yb3+ co-doped LaNbO4 phosphor (on excitation with 980 nm) by optimizing the concentrations of Eu3+ and Yb3+ ions. The downshifting (DS) behavior has been studied by photoluminescence (PL) measurements on excitation with 265 nm wavelength from a Xe lamp source. A broad blue emission in the region 300–550 nm with its maximum ∼415 nm due to charge transfer band (CTB) of the host and large number of sharp peaks due to f-f transitions of Eu3+ ion have been observed. The energy transfer has been observed from (NbO4)3‑ to Eu3+ ion and the fluorescence emission has been optimized by varying the concentration of Eu3+ ion. An intense red emission has also been observed corresponding to 5D0 → 7F2 transition of Eu3+ ion at 611 nm in LBO: 0.09Eu3+ phosphor on excitation with 394 nm. The luminescence properties of Eu3+ ion are enhanced further through the sensitization effect of Bi3+ ion. The near infra-red (NIR) quantum cutting (QC) behavior due to Yb3+ ion has been monitored on excitation with 265 as well as 394 nm. The NIR QC is observed due to 2F5/2 → 2F7/2 transition of Yb3+ ion via co-operative energy transfer (CET) process from (NbO4)3‑ as well as Eu3+ ions to Yb3+ ion. This multimodal behavior (UC, DS and QC) makes this a promising phosphor material for multi-purpose spectral converter.

Parametric study on co-precipitation of U/Th in MOX fuel of AHWR

International Nuclear Information System (INIS)

Tiwari, S.K.; Swaroopa Lakshmi, Y.; Nath, Baidurjya; Setty, D.S.; Kalyana Krishnan, G.; Saibaba, N.

2015-01-01

During manufacturing of Mixed Oxide Fuel (MOX) pellets for Advance Heavy Water Reactor (AHWR-LEU), around 30% rejected MOX pellets are generated in every cycle. These rejected MOX pellets are dissolved in nitric acid for recovery of U/Th. The recovered U/Th is recycled for production of MOX pellets. MOX pellets of varying compositions are used in AHWR fuel. Dissolution of MOX pellets in nitric acid is a challenging task because of its low surface area and longer dissolution times. High normal nitric acid is used in order to increase rate of dissolution, which in turn results in generation of high free acidity solution which influences the precipitation characteristics of Uranium (VI) by oxalic acid. Oxalic acid precipitation helps in generation of nitric acid which can be used for dissolution there by effectively facilitating nil effluent generation. Precipitation by oxalic acid unlike ammonia has advantage of zero liquid effluent discharge by complete recycle of oxalate filtrate to dissolution section. In the present work, the effect of various parameters like free acidity, residence time, concentration of oxalic acid, initial concentration of uranium and thorium etc. on the precipitation of U(VI) and Th(IV) in nitrate media by oxalic acid was carried out. The precipitated powder was subjected to various morphological evaluations like particle size etc. Study of various parameters on the co-precipitation of uranium and thorium by oxalic acid was carried out. It was observed that complete precipitation (> 99.9%) of thorium as oxalate does not depend on free acidity range (1- 6 N). Excess oxalic acid is not required for complete precipitation of thorium oxalate. The precipitation of uranyl oxalate varies with initial free acidity of solution. Uranyl oxalate precipitation does not take place at and above 5 N of free acidity

Electron beam induced green luminescence and degradation study of CaS:Ce nanocrystalline phosphors for FED applications

Energy Technology Data Exchange (ETDEWEB)

Kumar, Vinay, E-mail: vinaykdhiman@yahoo.com [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein 9300 (South Africa); Mishra, Varun [Department of Physics, Lovely Professional University, Phagwara 144 402, Punjab (India); Biggs, M.M.; Nagpure, I.M.; Ntwaeaborwa, O.M.; Terblans, J.J. [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein 9300 (South Africa); Swart, H.C., E-mail: swarthc.sci@ufs.ac.za [Department of Physics, University of the Free State, P.O. Box 339, Bloemfontein 9300 (South Africa)

2010-01-01

Green luminescence and degradation of Ce{sup 3+} doped CaS nanocrystalline phosphors were studied with a 2 keV, 10 {mu}A electron beam in an O{sub 2} environment. The nanophosphors were synthesized by the co-precipitation method. The samples were characterized using X-ray diffraction, Transmission electron microscopy, Scanning electron microscopy/electron dispersive X-ray spectroscopy and Photoluminescence (PL) spectroscopy. Cubic CaS with an average particle size of 42 {+-} 2 nm was obtained. PL emission was observed at 507 nm and a shoulder at 560 nm with an excitation wavelength of 460 nm. Auger electron spectroscopy and Cathodoluminescence (CL) were used to monitor the changes in the surface composition of the CaS:Ce{sup 3+} nanocrystalline phosphors during electron bombardment in an O{sub 2} environment. The effect of different oxygen pressures ranging from 1 x 10{sup -8} to 1 x 10{sup -6} Torr on the CL intensity was also investigated. A CaSO{sub 4} layer was observed on the surface after the electron beam degradation. The CL intensity was found to decrease up to 30% of its original intensity at 1 x 10{sup -6} Torr oxygen pressure after an electron dose of 50 C/cm{sup 2}. The formation of oxygen defects during electron bombardment may also be responsible for the decrease in CL intensity.

Electron beam induced green luminescence and degradation study of CaS:Ce nanocrystalline phosphors for FED applications

International Nuclear Information System (INIS)

Kumar, Vinay; Mishra, Varun; Biggs, M.M.; Nagpure, I.M.; Ntwaeaborwa, O.M.; Terblans, J.J.; Swart, H.C.

2010-01-01

Green luminescence and degradation of Ce 3+ doped CaS nanocrystalline phosphors were studied with a 2 keV, 10 μA electron beam in an O 2 environment. The nanophosphors were synthesized by the co-precipitation method. The samples were characterized using X-ray diffraction, Transmission electron microscopy, Scanning electron microscopy/electron dispersive X-ray spectroscopy and Photoluminescence (PL) spectroscopy. Cubic CaS with an average particle size of 42 ± 2 nm was obtained. PL emission was observed at 507 nm and a shoulder at 560 nm with an excitation wavelength of 460 nm. Auger electron spectroscopy and Cathodoluminescence (CL) were used to monitor the changes in the surface composition of the CaS:Ce 3+ nanocrystalline phosphors during electron bombardment in an O 2 environment. The effect of different oxygen pressures ranging from 1 x 10 -8 to 1 x 10 -6 Torr on the CL intensity was also investigated. A CaSO 4 layer was observed on the surface after the electron beam degradation. The CL intensity was found to decrease up to 30% of its original intensity at 1 x 10 -6 Torr oxygen pressure after an electron dose of 50 C/cm 2 . The formation of oxygen defects during electron bombardment may also be responsible for the decrease in CL intensity.

Down-conversion phosphors as noble-metal-free co-catalyst in ZnO for efficient visible light photocatalysis

Energy Technology Data Exchange (ETDEWEB)

Chu, Haipeng [Institute of Coordination Bond Metrology and Engineering, College of Materials Science and Engineering, China Jiliang University, Hangzhou 310018 (China); Liu, Xinjuan, E-mail: lxj669635@126.com [Institute of Coordination Bond Metrology and Engineering, College of Materials Science and Engineering, China Jiliang University, Hangzhou 310018 (China); Liu, Jiaqing [Engineering Research Center for Nanophotonics & Advanced Instrument, Ministry of Education, Department of Physics, East China Normal University, Shanghai 200062 (China); Lei, Wenyan [Institute of Coordination Bond Metrology and Engineering, College of Materials Science and Engineering, China Jiliang University, Hangzhou 310018 (China); Li, Jinliang [Engineering Research Center for Nanophotonics & Advanced Instrument, Ministry of Education, Department of Physics, East China Normal University, Shanghai 200062 (China); Wu, Tianyang [Institute of Coordination Bond Metrology and Engineering, College of Materials Science and Engineering, China Jiliang University, Hangzhou 310018 (China); Li, Ping [Shanghai Nanotechnology Promotion Center, Shanghai 200237 (China); Li, Huili; Pan, Likun [Engineering Research Center for Nanophotonics & Advanced Instrument, Ministry of Education, Department of Physics, East China Normal University, Shanghai 200062 (China)

2017-01-01

Graphical abstract: ZnO-Lu{sub 3}(Al,Si){sub 5}(O,N){sub 12}:Ce{sup 3+} hybrid photocatalysts were synthesized via a fast microwave-assisted approach for visible light photocatalytic degradation of organic pollutions with a high degradation rate of 91%. - Highlights: • ZnO-Lu{sub 3}(Al,Si){sub 5}(O,N){sub 12}:Ce{sup 3+} were synthesized via a facile microwave-assisted method. • Lu{sub 3}(Al,Si){sub 5}(O,N){sub 12}:Ce{sup 3+} acts as co-catalyst to facilitates the self-sensitized degradation of MB. • ZnO-Lu{sub 3}(Al,Si){sub 5}(O,N){sub 12}:Ce{sup 3+} exhibited enhanced visible light photocatalytic activity. • A high MB degradation rate of 91% was achieved under visible light irradiation. - Abstract: Exploring novel visible light responsive photocatalysts is one of greatly significant issues from the viewpoint of using solar energy. Here we report the yellow-orange emitting α-Si{sub 3}N{sub 4}-doped Lu{sub 3}Al{sub 5}O{sub 12}:Ce{sup 3+} (Lu{sub 3}Al{sub 5-x}Si{sub x}O{sub 12-x}N{sub x}:Ce{sup 3+}) phosphors as a noble-metal-free co-catalyst for enhanced visible light photocatalytic activity of ZnO. The results show that ZnO-Lu{sub 3}Al{sub 5-x}Si{sub x}O{sub 12-x}N{sub x}:Ce{sup 3+} hybrid photocatalysts using a fast microwave-assisted approach exhibits a 91% methylene blue (MB) degradation under visible light irradiation at 240 min, which evidence the synergistic effect of ZnO and Lu{sub 3}Al{sub 5-x}Si{sub x}O{sub 12-x}N{sub x}:Ce{sup 3+} that suppress the rate of charge recombination and increase the self-sensitized degradation of MB. ZnO-down conversion phosphors can be envisaged as potential candidate in environmental engineering and solar energy applications.

Chemical treatment of wastewaters produced during separation of iodine 131

International Nuclear Information System (INIS)

Cohen, P.; Marcaillou, J.; Amavis, R.

1959-01-01

The authors report the development and assessment of a chemical treatment of radioactive wastewaters by co-precipitation. This treatment is aimed at replacing a treatment based on the use of calcium phosphate which proved to be insufficient for wastewaters resulting from the production of iodine 131. After a presentation of the characteristics of the effluents to be processed, the authors report co-precipitation tests performed on effluents before release in the storage vessel (by using barium hydroxide, lead acetate or lead sulfate) and on effluents diluted on the storage vessel. They show that a co-precipitation method based on the use of lead sulfate in alkaline medium gives the best results

Mercury (II) reduction and co-precipitation of metallic mercury on hydrous ferric oxide in contaminated groundwater.

Science.gov (United States)

Richard, Jan-Helge; Bischoff, Cornelia; Ahrens, Christian G M; Biester, Harald

2016-01-01

Mercury (Hg) speciation and sorption analyses in contaminated aquifers are useful for understanding transformation, retention, and mobility of Hg in groundwater. In most aquifers hydrous ferric oxides (HFOs) are among the most important sorbents for trace metals; however, their role in sorption or mobilization of Hg in aquifers has been rarely analyzed. In this study, we investigated Hg chemistry and Hg sorption to HFO under changing redox conditions in a highly HgCl2-contaminated aquifer (up to 870μgL(-1) Hg). Results from aqueous and solid phase Hg measurements were compared to modeled (PHREEQC) data. Speciation analyses of dissolved mercury indicated that Hg(II) forms were reduced to Hg(0) under anoxic conditions, and adsorbed to or co-precipitated with HFO. Solid phase Hg thermo-desorption measurements revealed that between 55 and 93% of Hg bound to HFO was elemental Hg (Hg(0)). Hg concentrations in precipitates reached more than 4 weight %, up to 7000 times higher than predicted by geochemical models that do not consider unspecific sorption to and co-precipitation of elemental Hg with HFO. The observed process of Hg(II) reduction and Hg(0) formation, and its retention and co-precipitation by HFO is thought to be crucial in HgCl2-contaminated aquifers with variable redox-conditions regarding the related decrease in Hg solubility (factor of ~10(6)), and retention of Hg in the aquifer. Copyright © 2015 Elsevier B.V. All rights reserved.

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

Czech Academy of Sciences Publication Activity Database

Kameník, Jan; Amsil, H.; Kučera, Jan

2014-01-01

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

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)

Unactivated yttrium tantalate phosphor

International Nuclear Information System (INIS)

Reddy, V.B.; Cheung, H.K.

1992-01-01

This patent describes an unactivated yttrium tantalate phosphor having M prime monoclinic structure and containing one or more additives of Rb and Al in an amount of between about 0.001 to 0.1 moles per mole of yttrium tantalate to improve brightness under X-radiation. This patent also describes an unactivated yttrium tantalate phosphor having M prime monoclinic structure and containing additives of Sr in an amount of between 0.001 to 0.1 moles per mole of yttrium tantalate and one or more of Rb and Al in an amount of between 0.001 to 0.1 moles per mole of yttrium tantalate the phosphor exhibiting a greater brightness under X-radiation than the phosphor absent Rb and Al

Thermoluminescent dosimetry of new phosphors of Zn O exposed to beta radiation; Dosimetria termoluminiscente de nuevos fosforos de ZnO expuestos a radiacion beta

Energy Technology Data Exchange (ETDEWEB)

Cruz V, C.; Burruel I, S.E.; Grijalva M, H. [UNISON, A.P. 130, Hermosillo, Sonora (Mexico); Barboza F, M.; Bernal, R. [CIF, UNISON, A.P. 5-088, Hermosillo, Sonora (Mexico)

2004-07-01

In this work, we report the thermoluminescence dosimetry of a new Zn O phosphor obtained by annealing of Zn S powder precipitated when Zn S films were grown by employing a CBD method. The collected Zn S powder was pressed in a die to form pellets which were subjected to different thermal treatments under air atmosphere. X-ray diffraction (XRD) patterns and energy-dispersive X-ray Spectrometry (EDS) analyses confirmed the transformation of Zn S to Zn O. The phosphors thus obtained were exposed to high doses of beta radiation and their thermoluminescent dosimetry show that these new phosphors are materials suitable to be used in high dose thermoluminescence dosimetry. (Author)

On preparation of nanocrystalline chromites by co-precipitation and autocombustion methods

Energy Technology Data Exchange (ETDEWEB)

Matulkova, Irena [Department of Inorganic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 8, 128 43 Prague 2 (Czech Republic); Department of Radiation and Chemical Physics, Institute of Physics of the ASCR, v.v.i., Na Slovance 2, 182 21 Prague 8 (Czech Republic); Holec, Petr [Department of Inorganic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 8, 128 43 Prague 2 (Czech Republic); Department of Materials Chemistry, Institute of Inorganic Chemistry of the ASCR, v.v i., Husinec-Rez 1001, 250 68 Rez (Czech Republic); Pacakova, Barbara; Kubickova, Simona; Mantlikova, Alice [Department of Magnetic Nanosystems, Institute of Physics of the ASCR, v.v.i., Na Slovance 2, 182 21 Prague 8 (Czech Republic); Plocek, Jiri [Department of Materials Chemistry, Institute of Inorganic Chemistry of the ASCR, v.v i., Husinec-Rez 1001, 250 68 Rez (Czech Republic); Nemec, Ivan; Niznansky, Daniel [Department of Inorganic Chemistry, Faculty of Science, Charles University in Prague, Hlavova 8, 128 43 Prague 2 (Czech Republic); Vejpravova, Jana, E-mail: vejpravo@fzu.cz [Department of Magnetic Nanosystems, Institute of Physics of the ASCR, v.v.i., Na Slovance 2, 182 21 Prague 8 (Czech Republic)

2015-05-15

Highlights: • ACr{sub 2}O{sub 4} nanopowders, A = Cu, Fe, Ni, Mn and Mg were obtained in high yield. • Co-precipitation and autocombustion routes were optimized for single-phase product. • The nanopowders were examined by X-ray diffraction and vibrational spectroscopy. • Formation of cubic or tetragonal phase in Jahn–Teller NiCr{sub 2}O{sub 4} can be controlled. - Abstract: We present a comprehensive study on optimization of wet preparation routes yielding well-crystalline spinel chromite, ACr{sub 2}O{sub 4} nanoparticles (A = Cu, Fe, Ni, Mn and Mg). The auto-combustion and co-precipitation methods in the presence of nitrate or chloride ions and under different atmospheres, followed by annealing of final products at different temperatures were tested. All samples were characterized by powder X-ray diffraction (PXRD) and vibrational spectroscopy in order to evaluate their phase composition, particle size and micro-strain. Selected samples were subjected to investigation by transmission electron microscopy (TEM). The degree of the particle crystallinity was estimated by relating the apparent crystallite size obtained from the PXRD analysis to the physical grain size observed by the TEM. Optimal conditions leading to single-phase and highly-crystalline chromite nanoparticles are proposed.

Color tunable emission in Ce3+ and Tb3+ co-doped Ba2Ln(BO3)2Cl (Ln=Gd and Y) phosphors for white light-emitting diodes.

Science.gov (United States)

Zhang, Niumiao; Guo, Chongfeng; Jing, Heng; Jeong, Jung Hyun

2013-12-01

Ce(3+) and Tb(3+) co-doped Ba2Ln(BO3)2Cl (Ln=Y and Gd) green emitting phosphors were prepared by solid state reaction in reductive atmosphere. The emission and excitation spectra as well as luminescence decays were investigated, showing the occurrence of efficient energy transfer from Ce(3+) to Tb(3+) in this system. The phosphors exhibit both a blue emission from Ce(3+) and a green emission from Tb(3+) under near ultraviolet light excitation with 325-375 nm wavelength. Emission colors of phosphors could be tuned from deep blue through cyan to green by adjusting the Tb(3+) concentrations. The energy transfer efficiency and emission intensity of Ba2Y(BO3)2Cl:Ce(3+), Tb(3+) precede those of Ba2Gd(BO3)2Cl:Ce(3+), Tb(3+), and the sample Ba2Y(BO3)2Cl:0.03Ce(3+), 0.10Tb(3+) is the best candidate for n-UV LEDs. Copyright © 2013 Elsevier B.V. All rights reserved.

MBO3: Eu3+ at the rate SiO2 (M = Y, Gd and Al) nano down conversion phosphors with superior asymmetric ratio and colour purity as spectral converters for c-Si solar cells

International Nuclear Information System (INIS)

Rambabu, U.; Munirathnam, N.R.; Prakash, T.L.

2013-01-01

Y 1-x BO 3 :Eu x 3+ (0.07 ≤ x ≤ 0.5 mol) and Y 0.72x (Gd x , Al x )BO 3 : Eu 3+ 0.3 (0.05 ± x ± 0.3 mol) powder phosphors have been synthesized by a novel co-precipitation technique followed by heat treatment. Luminescence optimization was done: by optimizing the dopant Eu 3+ -concentration, substitution of Y 3+ with Gd 3+ /Al 3+ and finally with SiO 2 shell coating. Due to nanosize particle distribution, the optimum activator (Eu 3+ ) concentration (30 mol %) was found to be extremely at higher level, compared to the bulk phosphors. The asymmetric ratio (Red/Orange) and color purity of the optimized phosphors, Y 0.7 BO 3 :Eu 0.3 3+ (with crystallite size, D = 32 nm) and Y 0.3 Gd 0.2 Al 0.2 BO 3 :Eu 3+ (D = 17 nm) were further enhanced with SiO 2 shell coating. Based on the systematic study, the nanophosphor Y 0.7 BO 3 :Eu 0.3 3+ at the rate SiO 2 with R/O ratio as 6.710 and color coordinates (x = 0.6612, y = 0.3357) was optimized as a remarkable phosphor having superior features for its application in thin transparent form as DC layer to improve the energy conversion efficiency of c-Si solar cells

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

Czech Academy of Sciences Publication Activity Database

Kameník, Jan; Amsil, H.; Kučera, Jan

2015-01-01

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

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.

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

International Nuclear Information System (INIS)

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

1985-01-01

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

Ge{sup 4+}, Eu{sup 3+}-codoped Y{sub 2}SiO{sub 5} as a novel red phosphor for white LED applications

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yan; Dong, Yuanyuan [School of Materials Science and Engineering, Shanghai Institute of Technology, Shanghai 201418 (China); Wei, Bo [School of Chemistry and Materials Engineering, Changshu Institute of Technology, Changshu 215500 (China); Xu, Jiayue

2017-05-15

The phosphors Y{sub 2}SiO{sub 5}: Ge{sup 4+}, Eu{sup 3+} were synthesized by solid state reaction method assisted by flux, and have been characterized by X-ray powder diffraction and fluorescence spectrometer. The results showed that the phosphors can be effectively excited by near-UV (394 nm), and the major peak is located at 611 nm ascribed to the electric-dipole {sup 5}D{sub 0} → {sup 7}F{sub 2} transition of Eu{sup 3+}, the critical quenching concentration of Eu{sup 3+} in the phosphor is determined to be 15 mol% and the critical transfer distance is calculated as 8.90 Aa. Co-doping Y{sub 2}SiO{sub 5}: Eu{sup 3+} with Ge{sup 4+} helps to improve the luminescence intensity and color purity. The red emission of the phosphor under 394 nm excitation shows a good chromaticity index (0.652, 0.347) compared to commercial red phosphors Y{sub 2}O{sub 2}S: Eu{sup 3+} (0.631, 0.350). The quantum efficiency of the Y{sub 2}Si{sub 0.97}O{sub 5}: 0.03Ge{sup 4+}, 0.15Eu{sup 3+}phosphor under 394 nm excitation is estimated to be 45.24%. It can be concluded that efficient red light emitting diodes were fabricated using Ge{sup 4+}, Eu{sup 3+} co-doped phosphor based on near ultraviolet(NUV) excited LED lights. (copyright 2017 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

White light quality of phosphor converted light-emitting diodes: A phosphor materials perspective of view

International Nuclear Information System (INIS)

Sommer, Christian; Hartmann, Paul; Pachler, Peter; Hoschopf, Hans; Wenzl, Franz P.

2012-01-01

Highlights: ► We discuss the impact of the optical properties of a phosphor for colour temperature constancy in solid state lighting. ► Quantitative evaluation of permissible variations of the optical properties for batch-to-batch reproducibility. ► Quantitative evaluation of permissible variations of the optical properties upon temperature increase. ► Quantitative evaluation of permissible variations of the optical properties upon materials degradation. - Abstract: For a systematic approach to improve the white light quality of phosphor converted LEDs and to fulfil the demands for colour temperature reproducibility and constancy, it is imperative to understand how variations of the extinction coefficient and the quantum efficiency of the phosphor particles as well as variations of the excitation wavelength of the blue LED die affect the correlated colour temperature of the white LED source. Based on optical ray tracing of a phosphor converted white LED package we deduce permissible values for the variation of a given extinction coefficient and a given quantum efficiency of a phosphor material in order to maintain acceptable colour variations. These quantitative valuations of the required constancy of the optical properties of the phosphors will in particular provide some benchmarks for the synthesis of improved phosphor materials aiming at solid state lighting applications.

Moessbauer study of CO-precipitated Fischer-Tropsch iron catalysts

International Nuclear Information System (INIS)

Rao, K.R.P.M.; Huggins, F.E.; Mahajan, V.; Huffman, G.P.; Bukur, D.B.; Rao, V.U.S.

1994-01-01

Moessbauer spectroscopy studies of precipitated Fischer-Tropsch (FT) iron catalysts, viz. 100 Fe/5 Cu/4.2 K/x SiO 2 , where x = 0, 8, 16, 24, 25, 40, or 100, have shown that reduction of the oxide precursor in CO gives rise to χ-carbide Fe 5 C 2 whose amount decreases with an increase of SiO 2 content. The χ-carbide is converted into magnetite Fe 3 O 4 while catalyzing the FT synthesis reaction. A correlation between FT activity and the content of χ-carbide in the catalysts was found, which indicated that χ-carbide is active for FT synthesis reaction. (orig.)

Multi-model Projection of July-August Climate Extreme Changes over China under CO2 Doubling. Part Ⅰ:Precipitation

Institute of Scientific and Technical Information of China (English)

LI Hongmei; FENG Lei; ZHOU Tianjun

2011-01-01

Potential changes in precipitation extremes in July-August over China in response to CO2 doubling are analyzed based on the output of 24 coupled climate models from the Twentieth-Century Climate in Coupled Models (20C3M) experiment and the 1％ per year CO2 increase experiment (to doubling) (lpctto2x) of phase 3 of the Coupled Model Inter-comparison Project (CMIP3). Evaluation of the models' performance in simulating the mean state shows that the majority of models fairly reproduce the broad spatial pattern of observed precipitation. However, all the models underestimate extreme precipitation by ～50％. The spread among the models over the Tibetan Plateau is ～2-3 times larger than that over the other areas.Models with higher resolution generally perform better than those with lower resolutions in terms of spatial pattern and precipitation amount. Under the lpctto2x scenario, the ratio between the absolute value of MME extreme precipitation change and model spread is larger than that of total precipitation, indicating a relatively robust change of extremes. The change of extreme precipitation is more homogeneous than the total precipitation. Analysis on the output of Geophysical Fluid Dynamics Laboratory coupled climate model version 2.1 (GFDL-CM2.1) indicates that the spatially consistent increase of surface temperature and water vapor content contribute to the large increase of extreme precipitation over contiguous China,which follows the Clausius-Clapeyron relationship. Whereas, the meridionally tri-polar pattern of mean precipitation change over eastern China is dominated by the change of water vapor convergence, which is determined by the response of monsoon circulation to global warming.

Zinc and Carbonate Co-Substituted Nano-Hydroxyapatite

Science.gov (United States)

Girija, E. K.; Kumar, G. Suresh; Thamizhavel, A.

2011-07-01

Synthesis of Zn or CO32- substituted nano-hydroxyapatite (HA) and its physico-chemical properties have been well documented. However, the effects of the simultaneous substitution of Zn and CO32- in nano-HA have not been reported. In the present study, Zn and CO32- substitutions in nano HA independently and concurrently have been done by wet precipitation method and characterized by XRD and FT-IR for its phase purity and chemical homogeneity. Further modulations of the bioactivity and thermal stability of HA due to the substitutions have been studied.

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.

Role of Gd{sup 3+} ion on downshifting and upconversion emission properties of Pr{sup 3+}, Yb{sup 3+} co-doped YNbO{sub 4} phosphor and sensitization effect of Bi{sup 3+} ion

Energy Technology Data Exchange (ETDEWEB)

Dwivedi, A.; Rai, S. B., E-mail: sbrai49@yahoo.co.in [Department of Physics, Banaras Hindu University, Varanasi 221005 (India); Mishra, Kavita [Department of Physics, University of Lucknow, Lucknow 226007 (India)

2016-07-28

Dual-mode luminescence (downshifting-DS and upconversion-UC) properties of Pr{sup 3+}/Yb{sup 3+} co-doped Y{sub 1−x}Gd{sub x}NbO{sub 4} (x = 0.0, 0.5, and 1.0) phosphors synthesized by solid state reaction technique have been explored with and without Gd{sup 3+} ion. The structural characterizations (XRD, SEM, and FTIR) confirm the pure phase of YNbO{sub 4} phosphor. Further, with the Gd{sup 3+} ion co-doping, the YNbO{sub 4} phosphors having a random shape and the large particle size are found to be transformed into nearly spherical shape particles with the reduced particle size. The optical band gaps (E{sub g}) of Y{sub 1−x}Gd{sub x}NbO{sub 4} (x = 0.00, 0.25, 0.50, and 1.00) calculated from UV-Vis-NIR measurements are ∼3.69, 4.00, 4.38, and 4.44 eV, respectively. Moreover, YNbO{sub 4} phosphor is a promising blue emitting material, whereas Y{sub 1−x−y−z}Pr{sub y}Yb{sub z}Gd{sub x}NbO{sub 4} phosphor gives intense green, blue, and red emissions via dual-mode optical processes. The broad blue emission arises due to (NbO{sub 4}){sup 3−} group of the host with λ{sub ex} = 264 nm, whereas Pr{sup 3+} doped YNbO{sub 4} phosphor gives dominant red and blue emissions along with comparatively weak green emission on excitation with λ{sub ex} = 300 nm and 491 nm. The concentration dependent variation in emission intensity at 491 nm ({sup 3}P{sub 0}→{sup 3}H{sub 4} transition) and 612 nm ({sup 1}D{sub 2}→{sup 3}H{sub 4} transition); at 612 nm ({sup 1}D{sub 2}→{sup 3}H{sub 4} transition) and 658 nm ({sup 3}P{sub 0}→{sup 3}F{sub 2} transition) of Pr{sup 3+} ion in YNbO{sub 4} phosphor with λ{sub ex} = 300 nm and 491 nm excitations, respectively, has been thoroughly explored and explained by the cross-relaxation process through different channels. The sensitization effect of Bi{sup 3+} ion co-doping on DS properties of the phosphor has also been studied. The observed DS results have been optimized by varying the

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)

Radioluminescent nuclear batteries with different phosphor layers

International Nuclear Information System (INIS)

Hong, Liang; Tang, Xiao-Bin; Xu, Zhi-Heng; Liu, Yun-Peng; Chen, Da

2014-01-01

Highlights: • We present and test the electrical properties of the nuclear battery. • The best thickness range for ZnS:Cu phosphor layer is 12–14 mg cm −2 for 147 Pm radioisotope. • The best thickness range for Y 2 O 2 S:Eu phosphor layer is 17–21 mg cm −2147 Pm radioisotope. • The battery with ZnS:Cu phosphor layer can provide higher energy conversion efficiency. • The mechanism affecting the nuclear battery output performance is revealed. - Abstract: A radioluminescent nuclear battery based on the beta radioluminescence of phosphors is presented, and which consists of 147 Pm radioisotope, phosphor layers, and GaAs photovoltaic cell. ZnS:Cu and Y 2 O 2 S:Eu phosphor layers for various thickness were fabricated. To investigate the effect of phosphor layer parameters on the battery, the electrical properties were measured. Results indicate that the optimal thickness ranges for the ZnS:Cu and Y 2 O 2 S:Eu phosphor layers are 12 mg cm −2 to 14 mg cm −2 and 17 mg cm −2 to 21 mg cm −2 , respectively. ZnS:Cu phosphor layer exhibits higher fluorescence efficiency compared with the Y 2 O 2 S:Eu phosphor layer. Its spectrum properly matches the spectral response of GaAs photovoltaic cell. As a result, the battery with ZnS:Cu phosphor layer indicates higher energy conversion efficiency than that with Y 2 O 2 S:Eu phosphor layer. Additionally, the mechanism of the phosphor layer parameters that influence the output performance of the battery is discussed through the Monte Carlo method and transmissivity test

Uranium extraction from Uro area phosphate ore, Nuba mountains, Sudan

International Nuclear Information System (INIS)

Mohammed, A. A.; Eltayeb, M. A. H.

2003-01-01

This study was carried out mainly to extract uranium from Uro area phosphate ore in the eastern part of Nuba mountains near Abu Gibiha town in southern Kurdufan state. For this purpose first, the phosphate ore samples were decomposed with sulphuric acid. the resulting phosphoric acid was filtered off, and pretreated with pyrite and activated charcoal. the chemical analysis of the obtained grain phosphoric acid showed that about 98% of uranium content of the phosphate ore was rendered soluble in the phosphoric acid. The clear green phosphoric acid was introduced to uranium extraction by 25% tributylphosphate (Tbp) in kerosene. The effect of several factors on the extraction and stripping processes namely, interference's effect, the suitable strip solution, the required number of extraction and stripping stages, the optimum phase ratio have been studied in details. A three stage extraction at a phase ratio (aqueous/organic) of 1:2, followed by two stages stripping using 0.5 M sodium carbonate solution at a phase ratio (A/O) of 1:4 were found to be the optimum conditions to report more than 98% of uranium content in green phosphoric acid to the aqueous phase as uranyl tricarbonate complex (UO 2 (CO 3 ) 3 ) 4- . By applying sodica decomposition upon the stripping carbonate solution using 50% sodium hydroxide, about 98% of uranium content was precipitated as sodium diuranate concentrate (Na 2 U 2 O 7 ). The chemical analysis using atomic absorption spectrometry (Aas) showed a good agreement between the specification of the obtained uranium concentrate with the standard commercial specification of sodium diuranate concentrate. Further purification was achieved for the yellow cake by selective precipitation of uranium from the solution as uranium peroxide (UO 4 .2H 2 O) using 30% hydrogen peroxide. Finally the uranium peroxide precipitated was calcined at 450 degree C to obtain the orange powder uranium trioxide (UO 3 ). The chemical analysis of the final uranium trioxide

Effect of flux on the composition and luminescent properties of Ca{sub 0.68}Mg{sub 0.2}SiO{sub 3}:0.12Eu{sup 3+} red phosphor

Energy Technology Data Exchange (ETDEWEB)

Wang, Jin shan [College of Material Science and Engineering, Sichuan University, Chengdu 610065, Sichuan (China); Zhu, Da-chuan, E-mail: zdc89@163.com [College of Material Science and Engineering, Sichuan University, Chengdu 610065, Sichuan (China); Zheng, Qi [College of Material Science and Engineering, Sichuan University, Chengdu 610065, Sichuan (China); Han, Tao [Research Institute for New Materials Technology, Chongqing University of Arts and Sciences, Yongchuan 402160, Chongqing (China)

2016-11-15

Ca{sub 0.68}Mg{sub 0.2}SiO{sub 3}:0.12Eu{sup 3+} red-emitting phosphor was synthesized via one-step calcination process of the precursor prepared by chemical coprecipitation with different fluxes. Then X-ray diffraction and fluorescence spectrophotometry were adopted to investigate the structure and luminescent properties of Ca{sub 0.68}Mg{sub 0.2}SiO{sub 3}:0.12Eu{sup 3+}. The results indicated that adding fluxes increased the crystalline significantly while the phase composition of samples was not changed. Furthermore, the fluxes improved the intensity of emission peak and the quantum efficiency greatly. With the concentration of flux (Li{sub 2}CO{sub 3} or K{sub 2}CO{sub 3}) increasing, the emission intensity of Ca{sub 0.68}Mg{sub 0.2}SiO{sub 3}:0.12Eu{sup 3+} firstly increased and then decreased. Meanwhile, red-shift phenomenon was observed in the emission spectra. The optimal adding fraction of Li{sub 2}CO{sub 3} and K{sub 2}CO{sub 3} was 6% and 5% respectively, and the luminous intensity of samples calcined with the optimum adding amount of Li{sub 2}CO{sub 3}, K{sub 2}CO{sub 3} is 42 and 48 times that of the samples without flux. K{sub 2}CO{sub 3} showed a better effect on improving the emission intensity of the phosphors than Li{sub 2}CO{sub 3}.

Tuning Low Cycle Fatigue Properties of Cu-Be-Co-Ni Alloy by Precipitation Design

Directory of Open Access Journals (Sweden)

Yanchuan Tang

2018-06-01

Full Text Available As material for key parts applied in the aerospace field, the Cu-Be-Co-Ni alloy sustains cyclic plastic deformation in service, resulting in the low cycle fatigue (LCF failure. The LCF behaviors are closely related to the precipitation states of the alloy, but the specific relevance is still unknown. To provide reasonable regulation of the LCF properties for various service conditions, the effect of precipitation states on the LCF behaviors of the alloy was investigated. It is found that the alloy composed fully of non-shearable γ′ precipitates has higher fatigue crack initiation resistance, resulting in a longer fatigue life under LCF process with low total strain amplitude. The alloy with fine shearable γ′I precipitates presents higher fatigue crack propagation resistance, leading to a longer fatigue life under LCF process with high total strain amplitude. The cyclic stress response behavior of the alloy depends on the competition between the kinematic hardening and isotropic softening. The fine shearable γ′I precipitates retard the decrease of effective stress during cyclic loading, causing cyclic hardening of the alloy. The present work would help to design reasonable precipitation states of the alloy for various cyclic loading conditions to guarantee its safety in service.

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

Directory of Open Access Journals (Sweden)

Mohammad Misbah Khunur

2012-06-01

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

Fe-based soft magnetic composites coated with NiZn ferrite prepared by a co-precipitation method

Energy Technology Data Exchange (ETDEWEB)

Peng, Yuandong; Yi, Yi; Li, Liya; Ai, Hengyu; Wang, Xiaoxu [State Key Laboratory of Powder Metallurgy, Central South University, Changsha 410083 (China); Chen, Lulu [Jiangsu Eagle-globe Group Co., Ltd., Nantong 226600 (China)

2017-04-15

Fe powder was coated with NiZn ferrite by a co-precipitation method using chlorate as the raw material. Soft magnetic composites were manufactured via compaction and heat treatment of the coated powder. The coated powder and heat treated powder were analysed using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD) and Raman spectroscopy. Their magnetic properties were determined using a Quantum Design-Vibrating Sample Magnetometer (QD-VSM). The composites were analysed with SEM and EDS. The permeability and magnetic loss of the composites were measured with a B-H curve analyzer. The results show that, using the co-precipitation method, the raw precipitate was successfully prepared and coated the pure Fe powder and turned into spinel NiZn ferrite treated at 600 ℃ for 1 h. After heat treatment at 500 ℃ under air, the insulation coating layer of soft magnetic composite (SMC) was not destroyed and containing Fe, Ni, Zn and oxygen. The permeabilities of the SMC are stable at edge of the 2–200 kHz frequency range and the total loss was lower. - Graphical abstract: Scanning electron microscopy (SEM) images of Fe/(NiZn)Fe{sub 2}O{sub 4} composite powder heated at 600 ℃ for 1 h. - Highlights: • Fe particles were coated with (NiZn)Fe{sub 2}O{sub 4} via a co-precipitation and calcined method. • Coating layers were uniform and dense. • The permeabilities of the SMC are stable at edge of the 2–200 kHz frequency range.

Concentration and wavelength dependent frequency downshifting photoluminescence from a Tb3+ doped yttria nano-phosphor: A photochromic phosphor

Science.gov (United States)

Yadav, Ram Sagar; Rai, Shyam Bahadur

2018-03-01

In this article, the Tb3+ doped Y2O3 nano-phosphor has been synthesized through solution combustion method. The structural measurements of the nano-phosphor have been carried out by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) techniques, which reveal nano-crystalline nature. The Fourier transform infrared (FTIR) measurements reveal the presence of different molecular species in the nano-phosphor. The UV-Vis-NIR absorption spectrum of the nano-phosphor shows large number of bands due to charge transfer band (CTB) and 4f-4f electronic transitions of Tb3+ ion. The Tb3+ doped Y2O3 nano-phosphor emits intense green downshifting photoluminescence centered at 543 nm due to 5D4 → 7F5 transition on excitation with 350 nm. The emission intensity of the nano-phosphor is optimized at 1.0 mol% concentration of Tb3+ ion. When the as-synthesized nano-phosphor is annealed at higher temperature the emission intensity of the nano-phosphor enhances upto 5 times. The enhancement in the emission intensity is due to an increase in crystallinity of the nano-phosphor, reduction in surface defects and optical quenching centers. The CIE diagram reveals that the Tb3+ doped nano-phosphor samples show the photochromic nature (color tunability) with a change in the concentration of Tb3+ ion and excitation wavelength. The lifetime measurement indicates an increase in the lifetime for the annealed sample. Thus, the Tb3+ doped Y2O3 nano-phosphor may be used in photochromic displays and photonic devices.

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.

MULTI-PHOTON PHOSPHOR FEASIBILITY RESEARCH

Energy Technology Data Exchange (ETDEWEB)

R. Graham; W. Chow

2003-05-01

Development of multi-photon phosphor materials for discharge lamps represents a goal that would achieve up to a doubling of discharge (fluorescent) lamp efficacy. This report reviews the existing literature on multi-photon phosphors, identifies obstacles in developing such phosphors, and recommends directions for future research to address these obstacles. To critically examine issues involved in developing a multi-photon phosphor, the project brought together a team of experts from universities, national laboratories, and an industrial lamp manufacturer. Results and findings are organized into three categories: (1) Multi-Photon Systems and Processes, (2) Chemistry and Materials Issues, and (3) Concepts and Models. Multi-Photon Systems and Processes: This category focuses on how to use our current understanding of multi-photon phosphor systems to design new phosphor systems for application in fluorescent lamps. The quickest way to develop multi-photon lamp phosphors lies in finding sensitizer ions for Gd{sup 3+} and identifying activator ions to red shift the blue emission from Pr{sup 3+} due to the {sup 1}S{sub 0} {yields} {sup 1}I{sub 6} transition associated with the first cascading step. Success in either of these developments would lead to more efficient fluorescent lamps. Chemistry and Materials Issues: The most promising multi-photon phosphors are found in fluoride hosts. However, stability of fluorides in environments typically found in fluorescent lamps needs to be greatly improved. Experimental investigation of fluorides in actual lamp environments needs to be undertaken while working on oxide and oxyfluoride alternative systems for backup. Concepts and Models: Successful design of a multi-photon phosphor system based on cascading transitions of Gd{sup 3+} and Pr{sup 3+} depends critically on how the former can be sensitized and the latter can sensitize an activator ion. Methods to predict energy level diagrams and Judd-Ofelt parameters of multi

Phosphor blends for high-CRI fluorescent lamps

Science.gov (United States)

Setlur, Anant Achyut [Niskayuna, NY; Srivastava, Alok Mani [Niskayuna, NY; Comanzo, Holly Ann [Niskayuna, NY; Manivannan, Venkatesan [Clifton Park, NY; Beers, William Winder [Chesterland, OH; Toth, Katalin [Pomaz, HU; Balazs, Laszlo D [Budapest, HU

2008-06-24

A phosphor blend comprises at least two phosphors each selected from one of the groups of phosphors that absorb UV electromagnetic radiation and emit in a region of visible light. The phosphor blend can be applied to a discharge gas radiation source to produce light sources having high color rendering index. A phosphor blend is advantageously includes the phosphor (Tb,Y,LuLa,Gd).sub.x(Al,Ga).sub.yO.sub.12:Ce.sup.3+, wherein x is in the range from about 2.8 to and including 3 and y is in the range from about 4 to and including 5.

Continuous precipitation of mineral products: influence of mixing conditions on the co-precipitation of cerium-zirconium mixed oxides

International Nuclear Information System (INIS)

Di Patrizio, Nicolas

2015-01-01

An automated experimental set-up with rapid mixers is used to study the influence of mixing conditions on the co-precipitation of cerium-zirconium mixed oxides. The intensity of mixing is controlled by the inlet flow rates of the reacting solutions. An engulfment model is used to estimate a mixing time from the measurement of a segregation index by the Villermaux-Dushman reaction system. Three geometries of Hartridge Roughton mixers are compared. Mixing performance is better when a separate mixing chamber upstream of a narrower outlet pipe is present. A better mixing decreases the maximal reducibility temperature of the material and increases the crystal strains of the particles calcined at 1100 C. This is probably due to a better homogenization of the particles content. The important incorporation of nitrates in the particle at the outlet of the mixers shows precipitation occurs while the mixing process is not finished. This experimental result was confirmed by numerical simulation and an estimation of sur-saturations during the mixing process. (author)

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

Recovering uranium from phosphoric acid

International Nuclear Information System (INIS)

Anon.

1979-01-01

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

Magnetic behavior of nickel ferrite nanoparticles prepared by co-precipitation route

International Nuclear Information System (INIS)

Maaz, K.; Mashiatullah, A.; Javed, T.; Ali, G.; Karim, S.

2008-01-01

Magnetic nanoparticles of nickel ferrite (NiFe/sub 2/O/sub 4/) have been synthesized by co-precipitation route using stable ferric and nickel salts with sodium hydroxide as the precipitating agent and oleic acid as the surfactant. X-ray Diffraction (XRD) and Transmission Electron Microscope (TEM) analyses confirmed the formation of single phase nickel ferrite nanoparticles in the range 8-28 nm. The size of the particles was observed to be increasing linearly with increasing annealing temperature of the sample. Typical blocking effects were observed below -225 K for all the prepared samples. The superparamagnetic blocking temperature was found to be continuously increasing with increasing particle sizes that has been attributed to the increased effective anisotropy of the nanoparticles. The saturation moment of all the samples was found much below the bulk value of nickel ferrite that has been attributed to the disordered surface spins of these nanoparticles. (author)

Development, evaluation and optimization of superparamagnetite nanoparticles prepared by co-precipitation method.

Science.gov (United States)

Montaseri, Hashem; Alipour, Shohreh; Vakilinezhad, Molood Alsadat

2017-08-01

Magnetic nanoparticles (MNPs) are of high interest due to their application in medical fields, in particular for theranostics. Specific properties required for such particles include high magnetization, appropriate size and stability. Biocompatible magnetically soft magnetite particles (Fe 3 O 4 ) have been investigated for biological purposes. The intrinsic instability of these nanoparticles and their susceptibility to the oxidization in air, are limitations for their applications. Various methods have been described for synthesis of these nanoparticles among which co-precipitation method is widely experimented. In order to illustrate the synthesis of MNPs elaborately, the effect of different factors on particle formation were studied. The particles morphology, stability, paramagnetic effect, chemical structure and cytotoxicity were evaluated. Particles of 58 and 60 nm obtained by oleic acid coated (OMNPs) and citric acid coated (CMNPs) magnetite nanoparticles respectively. Transmission electron microscopy images exhibited the real sizes are 15 and 13 nm. Magnetic saturations of these nanoparticles were 72 and 68 emu/g which is suitable for medical applications. Both OMNPs and CMNPs were non-toxic to the SK-Br-3 and MCF-7 cells in the concentrations of <2.5 μg/mL. Since these particles exhibit relatively high magnetic saturation, low dose of such material would be required; therefore, these NPs seem to be suitable for theranostics.

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)

Solubility limit and precipitation kinetics of iron-phosphide in ferritic iron

International Nuclear Information System (INIS)

Suzuki, Shigeru

1992-01-01

The solubility limit of iron-phosphide in ferritic iron was examined with electrical resistivity measurements by using the relationship between resistivity and the amount of dissolved phosphorous. The temperature dependence of the solubility obtained was in good agreement with previous results. The kinetics of precipitation of the phosphide from a supersaturated Fe-3.75 at.% P alloy was also investigated with changes of the resistivity by isochronal and isothermal annealing. The activation energy for the precipitation process of the phosphide was about 2.6 eV. Diffusivities of phosphorus were estimated from the annealing behaviour and the morphology of the precipitates, which were comparable to those obtained with the tracer method previously. This suggests that the precipitation process of phosphide is rate controlled by diffusion of phosphorus in ferritic iron-phosphorus alloys. (orig.) [de

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.

Planar measurements of spray-induced wall cooling using phosphor thermometry

Science.gov (United States)

Dragomirov, Plamen; Mendieta, Aldo; Abram, Christopher; Fond, Benoît; Beyrau, Frank

2018-03-01

The wall cooling induced by spray impingement is investigated using phosphor thermometry. Thin coatings of zinc oxide (ZnO) phosphor were applied with a transparent chemical binder onto a steel surface. Instantaneous spatially resolved temperatures were determined using the spectral intensity ratio method directly after the injection of UV-grade hexane onto the surface using a commercial gasoline injector. The investigations showed that 2D temperature measurements with high spatial and shot-to-shot precision of, respectively, 0.5 and 0.6 K can be achieved, allowing the accurate resolution of the cooling induced by the spray. The presence of a liquid film over the phosphor coating during measurements showed no noticeable influence on the measured temperatures. However, in some cases a change in the intensity ratio at the spray impingement area, in the form of a permanent "stain", could be observed after multiple injections. The formation of this stain was less likely with increasing annealing time of the coating as well as lower plate operating temperatures during the injection experiments. Finally, the experimental results indicate a noticeable influence of the thickness of the phosphor coating on the measured spray-induced wall cooling history. Hence, for quantitative analysis, a compromise between coating thickness and measurement accuracy needs to be considered for similar applications where the heat transfer rates are very high.

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

Structural characterization of FeVO{sub 4} synthesized by co-precipitation method

Energy Technology Data Exchange (ETDEWEB)

Bera, Ganesh; Sinha, Sourav; Rambabu, P.; Das, P.; Gupta, A. K.; Turpu, G. R., E-mail: dr.tgreddy@gmail.com [Department of Pure and Applied Physics, Guru Ghasidas Vishwavidyalaya, Koni, Bilaspur 495 009 (India)

2016-05-06

A Low temperature method for synthesizing triclinic FeVO{sub 4} nanoparticles is manifested through co-precipitation method. Three precursor materials taken for the synthesis are Iron Nitrate, Ammonium Metavanadate and NaOH along with DI water. The attained precipitate was dried at 100°C for overnight and calcined at different temperatures ranging from 400°C - 650°C. The achieved powdered materials are studied through X-ray diffraction and found to be in pure single phase of P-1 space group symmetry. The crystallite size measured through Scherrer’s method is in found to be in the range of 40-60 nm. Raman spectroscopic studies were carried out at room temperature. Raman spectra is in agreement with the reported structural data of FeVO{sub 4}.

Chemical characteristics of surface systems in the Forsmark area. Visualisation and statistical evaluation of data from shallow groundwater, precipitation, and regolith

International Nuclear Information System (INIS)

Troejbom, Mats; Soederbaeck, Bjoern

2006-02-01

The Swedish Nuclear Fuel and Waste management Co (SKB) initiated site investigations for a deep repository for spent nuclear fuel at two different sites in Sweden, Forsmark and Oskarshamn, in 2002. This report evaluates the results from chemical investigations of the surface system in the Forsmark area during the period November 2002 - March 2005. The evaluation includes data from surface waters (lakes, streams and the sea), precipitation, shallow groundwater and regolith (till, soil, peat, sediments and biota) in the area. Results from surface waters are not presented in this report since these were treated in a recently published report. The main focus of the study is to visualize the vast amount of data collected hitherto in the site investigations, and to give a chemical characterisation of the investigated media at the site. The results will be used to support the site descriptive models, which in turn are used for safety assessment studies and for the environmental impact assessment. The data used consist of water chemical composition in lakes, streams, coastal sites, and in precipitation, predominantly sampled on a monthly basis, and in groundwater from soil tubes and wells, sampled up to four times per year. Moreover, regolith data includes information on the chemical composition of till, soil, sediment and vegetation samples from the area. The characterisations include all measured chemical parameters, i.e. major and minor constituents, trace elements, nutrients, isotopes and radio nuclides, as well as field measured parameters. The evaluation of data from each medium has been divided into the following parts: Characterisation of individual sampling sites, and comparisons within and among sampling sites as well as comparisons with local, regional and national reference data; Analysis of time trends and seasonal variation (for shallow groundwater); Exploration of relationships among the various chemical parameters. For all investigated parameters, the

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...

Phosphorous31 magnetic resonance spectroscopy after total sleep deprivation in healthy adult men.

Science.gov (United States)

Dorsey, Cynthia M; Lukas, Scott E; Moore, Constance M; Tartarini, Wendy L; Parow, Aimee M; Villafuerte, Rosemond A; Renshaw, Perry F

2003-08-01

To investigate chemical changes in the brains of healthy adults after sleep deprivation and recovery sleep, using phosphorous magnetic resonance spectroscopy. Three consecutive nights (baseline, sleep deprivation, recovery) were spent in the laboratory. Objective sleep measures were assessed on the baseline and recovery nights using polysomnography. Phosphorous magnetic resonance spectroscopy scans took place beginning at 7 am to 8 am on the morning after each of the 3 nights. Sleep laboratory in a private psychiatric teaching hospital. Eleven healthy young men. Following a baseline night of sleep, subjects underwent a night of total sleep deprivation, which involved supervision to ensure the absence of sleep but was not polysomnographically monitored. No significant changes in any measure of brain chemistry were observed the morning after a night of total sleep deprivation. However, after the recovery night, significant increases in total and beta-nucleoside triphosphate and decreases in phospholipid catabolism, measured by an increase in the concentration of glycerylphosphorylcholine, were observed. Chemical changes paralleled some changes in objective sleep measures. Significant chemical changes in the brain were observed following recovery sleep after 1 night of total sleep deprivation. The specific process underlying these changes is unclear due to the large brain region sampled in this exploratory study, but changes may reflect sleep inertia or some aspect of the homeostatic sleep mechanism that underlies the depletion and restoration of sleep. Phosphorous magnetic resonance spectroscopy is a technique that may be of value in further exploration of such sleep-wake functions.

The synthesis of hydroxyapatite through the precipitation method

International Nuclear Information System (INIS)

Shah Rizal, K.; Fahmi, M.N.; Mat Akil, H.; Zainal Arifin, A.

2004-01-01

Hydroxyapatite (HA) has been earmarked as suitable for implantation within the human body due to the similarity of its chemical makeup to human bone, In this paper, HA powders were synthesized via the precipitation method where phosphoric acid (H 3 PO 4 ) was titrated into calcium hydroxide solution [Ca(OH) 2 ]. Two parameters such as temperature and stirring rate were identified as factors that influenced the amount and purity of HA powder, Phase identification of the synthesized powder was done using X-Ray Diffraction (XRD). The results show that HA phase can be synthesized from this titration process of Ca(OH) 2 and H 3 PO 4 with yield amount of HA powder around 45-61 grams but with less than hundred percent purity. In order to study the effect of heat treatment to RA crystals structure, HA powder was calcined at 850 degree C for 2 hours. Its found that the degree of crystallinity increases after calcination because of lattice expansion when the materials were heated at higher temperature. (Author)

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

Chemical processing of liquid effluents in reprocessing plants: experience gained in France

International Nuclear Information System (INIS)

Fernandez, N.; Pottier, P.; Taillard, D.

1977-01-01

The radionuclides present in radioactive liquid effluents are precipitated for two purposes, viz: 1) to reduce the radioactivity to a level at which the liquids may be discharged; 2) to concentrate the radioactive compounds in the smallest possible volume for storage. The scientific principles of the radionuclide precipitation process are reviewed in the first part, which covers the solubility product, adsorption onto the surface of the precipitates, co-precipitation by isomorphism, ion-exchange on precipitates, etc. The paper goes on to discuss flocculation techniques, flocculation monitoring (zeta potential etc.) and methods of separating the solid and liquid phases. The specific methods for precipitating the main radionuclides are then described, with special reference to Sr, Cs, Ru, Co and Sb. The synergism of certain methods of precipitation is also discussed. The main part of the paper concerns the application of chemical processes for purifying low and medium active effluents in the Marcoule and La Hague centres. Particular emphasis is placed on the development of the processes used and the improvement of performance. Lastly, the paper discusses the possibilities offered in final treatment in such a way as to determine the limits to the effectiveness of the chemical processes. (orig.) [de

Chemical composition of precipitation in a Mexican Maya region

Science.gov (United States)

Bravo, H. A.; Saavedra, M. I. R.; Sánchez, P. A.; Torres, R. J.; Granada, L. M. M.

The chemical characteristics of wet precipitation in Puerto Morelos, Quintana Roo State, Mexico, were measured from April 1994 to December 1995. Puerto Morelos is located in the Caribbean Mayan coastal region of the Peninsula of Yucatan, and is normally exposed to winds from the Caribbean region. Wetfall was analyzed for pH, conductivity and Cl -, NO 3-, SO 42-, Na +, NH 4+, K +, Mg 2+ and Ca 2+ ion concentrations. Volume-weighted mean pH for the whole sampling period was 5.35, although values as low as 4.6 were measured in several rain samples. Concentrations of all species correlated negatively with rain volume. Sea-salt aerosols contributed with most of the Na +, Cl -, Mg 2+, K + and SO 42- found in wet precipitation. The mean [SO 42-excess] was 9.7 μEq l -1, which agrees with the background hemispheric values of ≈10 μEq l -1 reported elsewhere. The mean [NO 3-] was 11.4 μEq l -1, almost four times higher than the background hemispheric value of ≈2.5 μEq l -1 reported elsewhere. However, a major component causing the slight acidity character of rain in Puerto Morelos seems to be H 2SO 4.

Enhancement of metal-nanoparticle precipitation by co-irradiation of high-energy heavy ions and laser in silica glass

International Nuclear Information System (INIS)

Okubo, N.; Umeda, N.; Takeda, Y.; Kishimoto, N.

2003-01-01

Simultaneous laser irradiation under ion irradiation is conducted to control nanoparticle precipitation in amorphous (a-)SiO 2 . Copper ions of 3 MeV and photons of 532 nm by Nd:YAG laser are irradiated to substrates of a-SiO 2 . The ion dose rate and total dose are set at 2-10 μA/cm 2 and 3.0 x 10 16 -3.0 x 10 17 ions/cm 2 , respectively, and the laser power density is 0.05-0.2 J/cm 2 pulse at 10 Hz. The laser is simultaneously irradiated with ions in the co-irradiation mode, and the result is compared to that in the sequential and ion-only irradiation. Cross-sectional TEM of the irradiated specimens is conducted after measuring optical absorption spectra. In the case of co-irradiation of intense laser power and high dose (0.2 J/cm 2 pulse and 3.0 x 10 17 ions/cm 2 ), Cu nanoparticles precipitate much more extensively than in the sequential irradiation, increasing both the particle diameter and the total Cu atoms in the nanoparticles. The optical absorption spectra show a surface plasmon peak of the nanoparticles. The precipitation enhancement in the co-irradiation mode suggests that the electronic energy is absorbed by the dynamic electronic states and promotes the Cu precipitation via enhancing the atomic migration

Tuning the diurnal natural daylight with phosphor converted white LED – Advent of new phosphor blend composition

International Nuclear Information System (INIS)

Kim, Yoon Hwa; Arunkumar, Paulraj; Park, Seung Hyok; Yoon, Ho Shin; Im, Won Bin

2015-01-01

Highlights: • Designed phosphor blend that mimics diurnal daylight for health benefits. • Developed new phosphor blend composition that mimics natural sunlight under near UV. • The phosphor blend also exhibits high CRI (≥90) under blue LED excitation. • Fabricated WLED exhibited ∼91% spectral resemblance with daylight at 4500 K. • While ∼39.2% spectral resemblance were observed for YAG:Ce 3+ at 4500 K. - Abstract: We demonstrate the feasibility of developing phosphor converted white LED (pc-WLED) that mimics diurnal natural daylight with the newly designed phosphor blend in the color temperature (CCT) 2700–6000 K for health benefits. Natural daylight (sunlight) spectrum possesses broad emission in the visible region and closely approximates black body radiator, with color rendition index (CRI) of 100 under wide CCT (2500–6500 K). Current white light LEDs although are efficient and durable, they are not broad enough compared to daylight. We report new phosphor blend based on Sr 3 MgSi 2 O 8 :Eu 2+ blue phosphor with broad emission and high CRI ≥ 96 under both near UV and blue excitation. The fabricated WLED has exhibited ∼91% spectral resemblance with natural daylight compared to 39.2% for YAG:Ce 3+ white LED at 4500 K. The developed phosphor blend tunes the spectrum in wider CCT and would be a prospective candidate for full spectrum daylight WLED

Novel laser nanomaterials based on rare-earth compounds

Energy Technology Data Exchange (ETDEWEB)

Patel, Darayas N., E-mail: dpatel@oakwood.edu [Oakwood University, Department of Mathematics and Computer Science, 7000 Adventist Blvd. Huntsville, AL 35896 (United States); Hardy, Lauren A.; Smith, Tabatha J.; Smith, Eva S.; Wright, Donald M. [Oakwood University, Department of Mathematics and Computer Science, 7000 Adventist Blvd. Huntsville, AL 35896 (United States); Sarkisov, Sergey [SSS Optical Technologies, LLC, 515 Sparkman Drive, Suite 122, Huntsville, AL 35816 (United States)

2013-01-15

We report on the infrared-to-visible upconversion luminescence in microcrystalline powders and photonic crystal fibers filled with nanocolloids of trivalent rare-earth ion co-doped NaYF{sub 4} phosphor. The phosphor was prepared using a simple co-precipitation synthetic method. Nanocolloids of the phosphor were prepared by selective precipitation in methanol and laser ablation in water. Optical dynamic scatterometry determined average particle sizes of the nanocolloids of 1.5-1.9 nm in methanol and 83.8-86.4 nm in water. Nanocolloids of these phosphors were utilized as laser filling medium in photonic crystal fibers. - Highlights: Black-Right-Pointing-Pointer Synthesize highly efficient hexagonal-phase NaYF{sub 4}:Er{sup 3+}, Yb{sup 3+} powder and nanocolloid. Black-Right-Pointing-Pointer Laser/amplifier containing the NaYF{sub 4} nanocolloid were pumped with 980 nm diode laser. Black-Right-Pointing-Pointer Emission peaks were observed at 540 nm, 654 nm and 840.4 nm from the fiber arrangement.

Synthesis and characterization of the Y-type barium hexaferrite (Ba_2CoZnFe_1_2O_2_2) obtained by ultrasonic interdispersion of chemical precitates

International Nuclear Information System (INIS)

Junior, E.S.G.; Santos, M.R.C.; Jardim, P.M.; Ogasawara, T.; Almeida, L.H.

2011-01-01

This work is to study the synthesis and characterization of the Y-type barium hexaferrite powder (Ba2CoZnFe12O22) by chemical precipitation of the precursor materials Fe(OH)3, Co(OH)2, Zn(OH)2 and Ba(OH)2 separately and ultrasonic inter-dispersion, followed by drying and calcining. The study shows that the phase formation of the Y-type barium hexaferrite begins to emerge already at a temperature of 900 ° C with further phases still present, characterized by X-ray diffraction, the grain growth of the final product of the synthesis as a function of calcination temperature is visible by SEM, the measured magnetic of the powder through the hysteresis curve confirms that the material is magnetically soft at room temperature. The synthesis method developed in this research is an option to achieve the results that would be obtained if the co-precipitation of the ferric hydroxides, of cobalt, zinc and barium were thermodynamically possible. (author)

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

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.)

Radiation dosimetry using nano-BaSO{sub 4}:Eu

Energy Technology Data Exchange (ETDEWEB)

Pandey, A.; Sharma R, K. [University of Delhi, Department of Physics, Sri Venkateswara College, Benito Juarez Road, Dhaula Kuan, 110021 New Delhi (India); Bahl, S.; Kumar, P. [Medical Physics Unit, IRCH, AIIMS, 110029 New Delhi (India); Pal L, S., E-mail: apandey@svc.ac.in [Inter-University Accelerator Centre, Aruna Asaf Ali Marg, 110067 New Delhi (India)

2015-10-15

Nanocrystalline barium sulfate doped with europium (BaSO{sub 4}:Eu) was successfully prepared by the chemical co-precipitation technique and its thermoluminescence (Tl) dosimetry characteristics were studied for gamma radiation. Initially the dopant (Eu) concentration was varied, starting from 0.05 mol % to up to 1.00 mol %, and it was found that the nano phosphor BaSO{sub 4}:Eu with the dopant concentration of 0.2 mol % had the highest sensitivity within the given lot. The nano phosphor was also optimized for its annealing temperature in order to obtain the best results and was thereafter tested for its reusability and fading features. Further the nano phosphor was compared with the commercially available standard Tl dosimeter material LiF:Mg,Ti (popularly referred to as TLD-100) and it was found that the nano phosphor not only had a higher Tl sensitivity compared to the standard material over a wide range of doses but also had a Tl response which was linear even beyond the dose of 1 kGy. Linearity in Tl response to up to such high doses (∼1 kGy) is typical of nanocrystalline Tl phosphors. All the samples were irradiated by Co-60 source (having 1.25 MeV average energy) of gamma radiation. In order to test the energy independence of the nano phosphor (an important characteristic of an ideal Tl dosimeter) further studies are being carried out to examine the response of the nano phosphor to ionizing radiations of different energies. (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

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...

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)

Enhanced exciton emission from ZnO nano-phosphor induced by Yb3+ ions

CSIR Research Space (South Africa)

Kabongo, GL

2014-01-01

Full Text Available In this work, the sol–gel method was used to prepare Ytterbium (Yb(sup3+)) doped ZnO nano-phosphors with different concentrations of Yb(sup3+) ions. Their structural, morphological, photoluminescence, electronic states and the chemical composition...

Investigation of Synthesis and Magnetic Properties of Rod-Shaped CoFe2O4 via Precipitation-Topotactic Reaction Employing α-FeOOH and γ-FeOOH As Templates

Science.gov (United States)

Cao, Xiaohui; Dong, Hongfei; Tan, Yuzhuo; Meng, Jinhong

2018-03-01

Rod-shaped CoFe2O4 was prepared by chemical precipitation-topotactic reaction method, and in this preparation needle-like γ-FeOOH and α-FeOOH were synthesized to use as template materials. The evolution of phase and morphology in the process of calcination exhibits that α-FeOOH and γ-FeOOH experienced different routes to form the α-Fe2O3 middle phase with different crystallinity and morphology. The synthesis process of CoFe2O4 revealed that the crystallinity, purity and morphology of CoFe2O4 depend on the α-Fe2O3 middle phase. The magnetic measurement showed that the CoFe2O4 prepared from α-FeOOH has higher saturation magnetization and coercivity, and the crystallinity and morphology may play important roles in achieving a better magnetic performance.

Chemical composition of precipitation in a forest area of Chongqing, southwest China

International Nuclear Information System (INIS)

Zhang, F.; Zhang, J.; Zhang, H.; Ogura, N.; Ushikubo, A.

1996-01-01

Experiments were carried out in Chongqing - a city seriously damaged by acid precipitation in southwest China - to explore chemical compositions of open bulk precipitation, throughfall and stemflow in a Masson pine (Pinus massoniana) forest. The results showed that annual mean pH values of and annual ion depositions in the three types of rain water were 4.47 and 50.6 g m -2 , 3.82 and 69.7 g m -2 m and 2.92 and 0.215 g m -2 respectively. pH values demonstrated an obvious seasonal variation; they were lower in winter than in the rest of the year. Ca 2+ and NH 4 + together made up more than 80% of the total cation, while SO 4 2- alone contributed over 90% to the total anion. This high level of SO 4 2- in rain water in Congqing, which outran those found in other cities in China, was closely related to the combustion of locally produced coal that contains 3 to 5% sulphur. Thus, acid precipitation in Chongqing is of a typical sulphuric-acid type. 6 refs., 3 figs., 6 tabs

Precipitation kinetics of Mg-carbonates, influence of organic ligands and consequences for CO2 mineral sequestration

International Nuclear Information System (INIS)

Gautier, Q.

2012-01-01

Forming magnesium carbonate minerals through carbonation of magnesium silicates has been proposed as a safe and durable way to store carbon dioxide, with a possibly high potential to offset anthropogenic CO 2 emissions. To date however, chemical reactions involved in this process are facing strong kinetic limitations, which originate in the low reactivity of both Mg-silicates and Mg-carbonates. Numerous studies have focused on the dissolution of Mg-silicates, under the questionable hypothesis that this step limits the whole process. This thesis work focuses instead on the mechanisms and rates of formation of magnesium carbonates, which are the final products of carbonation reactions. The first part of the work is dedicated to studying the influence on magnesite precipitation kinetics of three organic ligands known to accelerate Mg-silicates dissolution rates: oxalate, citrate and EDTA. With help of mixed-flow reactor experiments performed between 100 and 150 C, we show that these ligands significantly reduce magnesite growth rates, through two combined mechanisms: (1) complexation of Mg 2+ cations in aqueous solution, which was rigorously estimated from a thermodynamic database established through a critical review of the literature, and (2) adsorption of ligands to a limited number of surface sites, leading to a decrease of the precipitation rate constant. The observed growth inhibition is maximal with citrate. We then used hydrothermal atomic force microscopy to probe the origin of the documented growth inhibition. Our observations show that citrate and oxalate interact with the crystal growth process on magnesite surface, modifying the shape of growth hillocks as well as the step generation frequency through spiral growth. We also show that the ligands adsorb preferentially on different kink-sites, which is probably related to their different structures and chemical properties. We propose that the stronger magnesite growth inhibition caused by citrate is related

Magnetic and structural properties of Cu{sub 0.85}Fe{sub 0.15}O system synthesized by co-precipitation

Energy Technology Data Exchange (ETDEWEB)

Colorado, H. D., E-mail: herdacom@gmail.com; Perez Alcazar, G. A. [Universidad del Valle, Departamento de Fisica (Colombia)

2011-11-15

Cu{sub 0.94}Fe{sub 0.06}O and Cu{sub 0.85}Fe{sub 0.15}O samples were synthesized by using the co-precipitation chemical method. Starting from aqueous solutions of copper nitrate, CuO (NO{sub 3}){sub 2} 3H{sub 2}O, iron nitrate, Fe (NO{sub 3}){sub 3} 9H{sub 2}O and sodium hydroxide as precipitating agent, NaOH. The precipitate of three samples for Cu{sub 0.94}Fe{sub 0.06}O and five for Cu{sub 0.85}Fe{sub 0.15}O of fine powder were calcined for 5 h at different temperatures. The obtained X rays diffraction patterns refined by the Rietveld method show the CuO characteristic pattern, showing that the Fe atoms enter to replace Cu atoms. Furthermore, it was obtained that the crystallite size decreases with calcination temperatures for Cu{sub 0.94}Fe{sub 0.06}O. The transmission Moessbauer spectroscopy showed that the samples present a disordered paramagnetic behavior due to the big value of the half-width of line of the quadrupolar splitting. Vibrating sample magnetometry confirms the paramagnetic character. The XRD results indicate that the material is nanostructured, due that the crystallite sizes are of the order of 10 nm for Cu{sub 0.94}Fe{sub 0.06}O and 40 nm for Cu{sub 0.85}Fe{sub 0.15}O.

Dosimetry characteristics of thermoluminescent Li2B4O7:Cu phosphor

International Nuclear Information System (INIS)

Lakshmanan, A.R.; Chandra, B.; Bhatt, R.C.

1981-01-01

Preliminary investigations on the radiation dosimetry characteristics of Li 2 B 4 O 7 :Cu TLD phosphor are described. The major TL peak in this phosphor occurs at 230 0 C and its TL sensitivity to gamma radiation is two to three times higher than that of LiF TLD-100. The gamma dose Vs TL response of this peak is linear (within +- 20%) in the dose range 0.3 mGy-3x10 2 Gy above which saturation sets in. Its TL response for 30 keV X-rays is about 20% lower than that for 60 Coγ-rays. On annealing at 300 0 C, the phosphor gets slightly discoloured (brownish). This results in the reduction of the TL sensitivity by about 20 - 25%. The phosphor does not exhibit either sensitization or damage even after a gamma dose of 10 3 Gy. The TL emission spectrum has a broad peak at 360 nm. The intrinsic TL sensitivity of virgin Li 2 B 4 O 7 :Cu to 253.7 nm UV radiation is nearly 50 times higher than that of CaSO 4 :Dy. The post-irradiation fading in Li 2 B 4 O 7 :Cu at ambient temperature and humidity conditions is, however, less than 10% in 17 days. These characteristics indicate that Li 2 B 4 O 7 :Cu is a promising phosphor for ionizing as well as UV radiation dosimetry. (author)

Green and red luminescence in co-precipitation synthesized Pr:LuAG nanophosphor

Energy Technology Data Exchange (ETDEWEB)

Kumar, S. Arun; Kumar, K. Ashok; Gunaseelan, M.; Senthilselvan, J., E-mail: jsselvan@hotmail.com [Department of Nuclear Physics, University of Madras, Guindy Campus, Chennai–600 025, Tamil Nadu (India); Asokan, K. [Materials Science Group, Inter University Accelerator Centre, New Delhi-110067 (India)

2016-05-06

Pr:LuAG nanophosphor is an effective candidate in magnetic resonance imaging coupled positron emission tomography (MRI-PET) for medical imaging and scintillator applications. LuAG:Pr (0.05, 0.15 mol%) nanoscale ceramic powders were synthesized by co-precipitation method using urea as precipitant. Effect of antisite defect on structure and luminescence behavior was investigated. Pr:LuAG nanoceramic powders are found crystallized in cubic structure by high temperature calcination at 1400 °C and it shows antisite defect. HR-SEM analysis revealed spherically shaped Pr:LuAG nanoceramic particulate powders with ∼100 nm size. By the excitation at 450 nm, Pr:LuAG nanophosphor exhibit green to red luminescence in the wavelength range of 520 to 680 nm, which is originated from multiplet transition of Pr{sup 3+} ions.

Tuning the diurnal natural daylight with phosphor converted white LED – Advent of new phosphor blend composition

Energy Technology Data Exchange (ETDEWEB)

Kim, Yoon Hwa [School of Materials Science and Engineering, Chonnam National University, 300, Yongbong-dong, Buk-gu, Gwangju 500-757 (Korea, Republic of); Research Institute, Force4 Corp., Daechon-dong, Buk-gu, Gwangju 500-470 (Korea, Republic of); Arunkumar, Paulraj [School of Materials Science and Engineering, Chonnam National University, 300, Yongbong-dong, Buk-gu, Gwangju 500-757 (Korea, Republic of); Park, Seung Hyok; Yoon, Ho Shin [Research Institute, Force4 Corp., Daechon-dong, Buk-gu, Gwangju 500-470 (Korea, Republic of); Im, Won Bin, E-mail: imwonbin@jnu.ac.kr [School of Materials Science and Engineering, Chonnam National University, 300, Yongbong-dong, Buk-gu, Gwangju 500-757 (Korea, Republic of)

2015-03-15

Highlights: • Designed phosphor blend that mimics diurnal daylight for health benefits. • Developed new phosphor blend composition that mimics natural sunlight under near UV. • The phosphor blend also exhibits high CRI (≥90) under blue LED excitation. • Fabricated WLED exhibited ∼91% spectral resemblance with daylight at 4500 K. • While ∼39.2% spectral resemblance were observed for YAG:Ce{sup 3+} at 4500 K. - Abstract: We demonstrate the feasibility of developing phosphor converted white LED (pc-WLED) that mimics diurnal natural daylight with the newly designed phosphor blend in the color temperature (CCT) 2700–6000 K for health benefits. Natural daylight (sunlight) spectrum possesses broad emission in the visible region and closely approximates black body radiator, with color rendition index (CRI) of 100 under wide CCT (2500–6500 K). Current white light LEDs although are efficient and durable, they are not broad enough compared to daylight. We report new phosphor blend based on Sr{sub 3}MgSi{sub 2}O{sub 8}:Eu{sup 2+} blue phosphor with broad emission and high CRI ≥ 96 under both near UV and blue excitation. The fabricated WLED has exhibited ∼91% spectral resemblance with natural daylight compared to 39.2% for YAG:Ce{sup 3+} white LED at 4500 K. The developed phosphor blend tunes the spectrum in wider CCT and would be a prospective candidate for full spectrum daylight WLED.

Potential tunable white-emitting phosphor LiSr4(BO3)3:Ce3+, Eu2+ for ultraviolet light-emitting diodes

International Nuclear Information System (INIS)

Wang Qian; Deng Degang; Hua Youjie; Huang Lihui; Wang Huanping; Zhao Shilong; Jia Guohua; Li Chenxia; Xu Shiqing

2012-01-01

A novel Ce 3+ /Eu 2+ co-activated LiSr 4 (BO 3 ) 3 phosphor has been synthesized by traditional solid-state reaction. The samples could display varied color emission from blue towards white and ultimately to yellow under the excitation of ultraviolet (UV) light with the appropriate adjustment of the relative proportion of Ce 3+ /Eu 2+ . The resonance-type energy transfer mechanism from Ce 3+ to Eu 2+ in LiSr 4 (BO 3 ) 3 :Ce 3+ , Eu 2+ phosphors is dominant by electric dipole–dipole interaction, and the critical distance is calculated to be about 29.14 Å by the spectra overlap method. White light was observed from LiSr 4 (BO 3 ) 3 :mCe 3+ , nEu 2+ phosphors with chromaticity coordinates (0.34, 0.30) upon 350 nm excitation. The LiSr 4 (BO 3 ) 3 :Ce 3+ , Eu 2+ phosphor has potential applications as an UV radiation-converting phosphor for white light-emitting diodes. - Highlights: ► White light was observed from the novel phosphor with chromaticity coordinate (0.34, 0.30). ► Resonant energy transfer between Ce 3+ and Eu 2+ occurs in the novel phosphor. ► This novel phosphor has potential applications as a UV-driven light-emitting phosphor.

Color stable manganese-doped phosphors

Science.gov (United States)

Lyons, Robert Joseph [Burnt Hills, NY; Setlur, Anant Achyut [Niskayuna, NY; Deshpande, Anirudha Rajendra [Twinsburg, OH; Grigorov, Ljudmil Slavchev [Sofia, BG

2012-08-28

A process for preparing color stable Mn.sup.+4 doped phosphors includes providing a phosphor of formula I; A.sub.x[MF.sub.y]:Mn.sup.+4 I and contacting the phosphor in particulate form with a saturated solution of a composition of formula II in aqueous hydrofluoric acid; A.sub.x[MF.sub.y]; II wherein A is Li, Na, K, Rb, Cs, NR.sub.4 or a combination thereof; M is Si, Ge, Sn, Ti, Zr, Al, Ga, In, Sc, Y, La, Nb, Ta, Bi, Gd, or a combination thereof; R is H, lower alkyl, or a combination thereof; x is the absolute value of the charge of the [MF.sub.y] ion; and y is 5, 6 or 7. In particular embodiments, M is Si, Ge, Sn, Ti, Zr, or a combination thereof. A lighting apparatus capable of emitting white light includes a semiconductor light source; and a phosphor composition radiationally coupled to the light source, and which includes a color stable Mn.sup.+4 doped phosphor.

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

Improvements in x-ray image converters and phosphors

International Nuclear Information System (INIS)

Rabatin, J.G.

1981-01-01

Improvements to an X-ray image converter comprising crystals of rare earth phosphor admixtures are described. The phosphor admixtures utilize thulium-activated lanthanum and/or gadolinium oxyhalide phosphor material to increase the relative speed and resolution of an X-ray image compared with conventional rare earth phosphors. Examples of various radiographic screens containing one or more of the phosphor materials are given. (U.K.)

Fluorescent lighting with aluminum nitride phosphors

Science.gov (United States)

Cherepy, Nerine J.; Payne, Stephen A.; Seeley, Zachary M.; Srivastava, Alok M.

2016-05-10

A fluorescent lamp includes a glass envelope; at least two electrodes connected to the glass envelope; mercury vapor and an inert gas within the glass envelope; and a phosphor within the glass envelope, wherein the phosphor blend includes aluminum nitride. The phosphor may be a wurtzite (hexagonal) crystalline structure Al.sub.(1-x)M.sub.xN phosphor, where M may be drawn from beryllium, magnesium, calcium, strontium, barium, zinc, scandium, yttrium, lanthanum, cerium, praseodymium, europium, gadolinium, terbium, ytterbium, bismuth, manganese, silicon, germanium, tin, boron, or gallium is synthesized to include dopants to control its luminescence under ultraviolet excitation. The disclosed Al.sub.(1-x)M.sub.xN:Mn phosphor provides bright orange-red emission, comparable in efficiency and spectrum to that of the standard orange-red phosphor used in fluorescent lighting, Y.sub.2O.sub.3:Eu. Furthermore, it offers excellent lumen maintenance in a fluorescent lamp, and does not utilize "critical rare earths," minimizing sensitivity to fluctuating market prices for the rare earth elements.

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).

Preparation of CaSO4:Dy by precipitation method to gamma radiation dosimetry

International Nuclear Information System (INIS)

Rivera, T.; Roman, J.; Azorin, J.; Sosa, R.; Guzman, J.; Serrano, A.K.; Garcia, M.; Alarcon, G.

2010-01-01

This paper presents the results of the preparation and characterization of dysprosium-doped calcium sulfate (CaSO 4 :Dy) phosphor, which was obtained by homogeneous precipitation from calcium acetate Ca(CH 3 COO - ) 2 . Structural and morphological characteristics were studied using a scanning electronic microscope (SEM). The structure of all compounds was determined by X-ray diffraction method too. Thermoluminescence (TL) emission properties of CaSO 4 :Dy under gamma radiation effects were studied. This phosphor powder presented a TL glow curve with two peaks (Tmax) centered at around of 180 and 300 deg. C, respectively. The TL response of CaSO 4 :Dy as a function of gamma absorbed dose was linear in a wide range. Both emission and excitation spectra were also obtained. Results showed that this new preparation method of CaSO 4 :Dy TL phosphor is less expensive, cleaner and safer than the conventional preparation method.

Comparison of Four Strong Acids on the Precipitation Potential of Gypsum in Brines During Distillation of Pretreated, Augmented Urine

Science.gov (United States)

Muirhead, Dean; Carrier, Christopher

2012-01-01

In this study, three different mineral acids were substituted for sulfuric acid (H2SO4) in the urine stabilizer solution to eliminate the excess of sulfate ions in pretreated urine and assess the impact on maximum water recovery to avoid precipitation of minerals during distillation. The study evaluated replacing 98% sulfuric acid with 85% phosphoric acid (H3PO4), 37% hydrochloric acid (HCl), or 70% nitric acid (HNO3). The effect of lowering the oxidizer concentration in the pretreatment formulation also was studied. This paper summarizes the test results, defines candidate formulations for further study, and specifies the injection masses required to stabilize urine and minimize the risk of mineral precipitation during distillation. In the first test with a brine ersatz acidified with different acids, the solubility of calcium in gypsum saturated solutions was measured. The solubility of gypsum was doubled in the brines acidified with the alternative acids compared to sulfuric acid. In a second series of tests, the alternative acid pretreatment concentrations were effective at preventing precipitation of gypsum and other minerals up to 85% water recovery from 95th-percentile pretreated, augmented urine. Based on test results, phosphoric acid is recommended as the safest alternative to sulfuric acid. It also is recommended that the injected mass concentration of chromium trioxide solution be reduced by 75% to minimize liquid resupply mass by about 50%, reduce toxicity of brines, and reduce the concentration of organic acids in distillate. The new stabilizer solution formulations and required doses to stabilize urine and prevent precipitation of minerals up to 85% water recovery are given. The formulations in this study were tested on a limited number of artificially augmented urine batches collected from employees at the Johnson Space Center (JSC). This study successfully demonstrated that the desired physical and chemical stability of pretreated urine and brines

A study of CO2 precipitation method considering an ionic CO2 and Ca(OH)2 slurry

International Nuclear Information System (INIS)

Park, Sangwon; Jo, Hoyong; Kang, Dongwoo; Park, Jinwon

2014-01-01

CCS (carbon capture and storage) is the most popular technology used for the reduction of CO 2 in the post-combustion stage. However, the CCS process has some disadvantages including uncertainty about the stability of the land that is used to store the separated CO 2 . Consequently, CCU (carbon capture and utilization) technologies have recently received increased attention as a possible replacement for CCS. In this study, we utilized CO 2 fixation methods by using the metal carbonate mechanism. We selected 5 and 30 wt% MEA (mono-ethanolamine) solutions to rapidly make a carbonate and Ca(OH) 2 slurry. In all of the experiments, normal temperature and pressure conditions were maintained (except during desorption to check for residual CO 2 in the MEA solution). Consequently, most of the CO 2 was converted to carbonate. The MEA converted CO 2 to ionic CO 2 and rapidly created calcium carbonate. Also the formed solids that were observed were determined to be CaCO 3 and Ca(OH) 2 by X-ray diffractometry. Also, the MEA solution could be reused to absorb CO 2 . Therefore, we have confirmed the development of our suggested CCS process. This process has the ability not only to reuse emitted CO 2 , but it can also be employed to reuse construction wastes that include heavy metals. - Highlights: • We propose novel CO 2 conversion technology by utilizing an amine solution. • In this study, alkaline solutions were used to produce CO 2 precipitate. • The MEA (mono-ethanolamine) solution has a sufficient potential to fix CO 2 with metal sources under moderate condition. • Also, the Ca(OH) 2 slurry yielded enough Ca 2+ ions to make carbonate

Polycrystalline Silicon Gettered by Porous Silicon and Heavy Phosphorous Diffusion

Institute of Scientific and Technical Information of China (English)

LIU Zuming(刘祖明); Souleymane K Traore; ZHANG Zhongwen(张忠文); LUO Yi(罗毅)

2004-01-01

The biggest barrier for photovoltaic (PV) utilization is its high cost, so the key for scale PV utilization is to further decrease the cost of solar cells. One way to improve the efficiency, and therefore lower the cost, is to increase the minority carrier lifetime by controlling the material defects. The main defects in grain boundaries of polycrystalline silicon gettered by porous silicon and heavy phosphorous diffusion have been studied. The porous silicon was formed on the two surfaces of wafers by chemical etching. Phosphorous was then diffused into the wafers at high temperature (900℃). After the porous silicon and diffusion layers were removed, the minority carrier lifetime was measured by photo-conductor decay. The results show that the lifetime's minority carriers are increased greatly after such treatment.

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)

Use of glucose as reductant to recover Co from spent lithium ions batteries.

Science.gov (United States)

Meng, Qi; Zhang, Yingjie; Dong, Peng

2017-06-01

A hydrometallurgical leaching process has been developed for recovery of Co and Li from cathode material (LiCoO 2 ) collected from spent LIBs using a mix solution of glucose and phosphoric acid. The spent LiCoO 2 before and after leaching process are analyzed by scanning electron microscopy. A leaching rate of about 98% Co and nearly 100% Li is presented with 1.5mol/L phosphoric acid and 0.02mol/L glucose at 80°C in about 2h. During leaching process, glucose was oxidized into monocarboxylic acid with reduction of Co(III) to Co(II). Co in solution was recovered as Co-oxalate after leaching process. Using glucose as reductant to dissolve LiCoO 2 with chelating agent of phosphoric acid is achieved here. Copyright © 2017 Elsevier Ltd. All rights reserved.

In-Drift Precipitates/Salts Model

International Nuclear Information System (INIS)

P. Mariner

2004-01-01

This report documents the development and validation of the in-drift precipitates/salts (IDPS) model. The IDPS model is a geochemical model designed to predict the postclosure effects of evaporation and deliquescence on the chemical composition of water within the Engineered Barrier System (EBS) in support of the Total System Performance Assessment for the License Application (TSPA-LA). Application of the model in support of TSPA-LA is documented in ''Engineered Barrier System: Physical and Chemical Environment Model'' (BSC 2004 [DIRS 169860]). Technical Work Plan for: Near-Field Environment and Transport In-Drift Geochemistry Model Report Integration (BSC 2004 [DIRS 171156]) is the technical work plan (TWP) for this report. It called for a revision of the previous version of the report (BSC 2004 [DIRS 167734]) to achieve greater transparency, readability, data traceability, and report integration. The intended use of the IDPS model is to estimate and tabulate, within an appropriate level of confidence, the effects of evaporation, deliquescence, and potential environmental conditions on the pH, ionic strength, and chemical compositions of water and minerals on the drip shield or other location within the drift during the postclosure period. Specifically, the intended use is as follows: (1) To estimate, within an appropriate level of confidence, the effects of evaporation and deliquescence on the presence and composition of water occurring within the repository during the postclosure period (i.e., effects on pH, ionic strength, deliquescence relative humidity, total concentrations of dissolved components in the system Na-K-H-Mg-Ca-Al-Cl-F-NO 3 -SO 4 -Br-CO 3 -SiO 2 -CO 2 -O 2 -H 2 O, and concentrations of the following aqueous species that potentially affect acid neutralizing capacity: HCO 3 - , CO 3 2- , OH - , H + , HSO 4 - , Ca 2+ , Mg 2+ , CaHCO 3 + , MgHCO 3 + , HSiO 3 - , and MgOH + ); (2) To estimate, within an appropriate level of confidence, mineral

Phosphors for X-ray intensification screens

International Nuclear Information System (INIS)