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

International Nuclear Information System (INIS)

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

1989-01-01

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

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

International Nuclear Information System (INIS)

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

1994-01-01

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

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

International Nuclear Information System (INIS)

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

2010-01-01

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

Synergistic solvent extraction investigation of Am (III), Eu (III), Zn(II), and Cs(I), using 2-heptyl-2-methyl-nonanoic acid mixed with different organophosphorus compounds from nitrate media. Vol. 3

Energy Technology Data Exchange (ETDEWEB)

El-Naggar, H A; Ramadan, A; Abdel-Fattah, A [Nuclear Chemistry Department, Hot Laboratories Center, Atomic Energy Authority, Cairo (Egypt)

1996-03-01

Extraction studies for investigating the effect of mixing 2-heptyl-2-methyl nonanoic acid (HA) with a number of organophosphorus compounds; namely tributyl phosphate (TBP), terphenyl phosphate oxide (TPPO); tri octyl phosphine oxide (TOPO) or bis-2-(ethyl hexyl) phosphoric acid (HDEHP) in benzene on the extraction of trace elements Am(III), Eu(III), Zn(II), and Cs(I) from nitrate media of ionic strength, I=0.1 M were carried out. The effect of adding different organophosphorus compounds to HA was tested to account for the presence or absence of the phenomenon of synergism. It was found that TBP, TPPO, and TOPO causing some antagonistic effects for the elements studied. Extraction enhancement was only observed with bis- (2-ethyl-hexyl) -phosphoric acid (HDEHP) for all the elements investigated. The extraction mechanisms as well as the thermodynamic parameters for the mixed extracted species are discussed. 19 figs.

Synergistic solvent extraction investigation of Am (III), Eu (III), Zn(II), and Cs(I), using 2-heptyl-2-methyl-nonanoic acid mixed with different organophosphorus compounds from nitrate media. Vol. 3

International Nuclear Information System (INIS)

El-Naggar, H.A.; Ramadan, A.; Abdel-Fattah, A.

1996-01-01

Extraction studies for investigating the effect of mixing 2-heptyl-2-methyl nonanoic acid (HA) with a number of organophosphorus compounds; namely tributyl phosphate (TBP), terphenyl phosphate oxide (TPPO); tri octyl phosphine oxide (TOPO) or bis-2-(ethyl hexyl) phosphoric acid (HDEHP) in benzene on the extraction of trace elements Am(III), Eu(III), Zn(II), and Cs(I) from nitrate media of ionic strength, I=0.1 M were carried out. The effect of adding different organophosphorus compounds to HA was tested to account for the presence or absence of the phenomenon of synergism. It was found that TBP, TPPO, and TOPO causing some antagonistic effects for the elements studied. Extraction enhancement was only observed with bis- (2-ethyl-hexyl) -phosphoric acid (HDEHP) for all the elements investigated. The extraction mechanisms as well as the thermodynamic parameters for the mixed extracted species are discussed. 19 figs

Uranium extraction from colofanite via organic solvents

International Nuclear Information System (INIS)

Ribeiro, Valeria Aparecida Leitao

2007-01-01

This work describes the use of pure or combined extractants dissolved in organic solvents for quantitative uranium recovery from colofanite, a fluoroapatite ore, from Itataia, Santa Quiteria, Ceara, Brazil. This ore contains the highest brazilian uranium reserve. The metal is associated to phosphate species. The ore is digested with sulfuric acid (wet process), producing phosphoric acid, which is used for manufacturing of fertilizers and animal food. >From the acid leaching, some systems for uranium recovery were tested. Among them, PC88A (2-ethyl-hexyl phosphonic acid, mono-2-ethyl-hexyl ester) 40% vol. and DEHPA (di(2-ethyl-hexyl)phosphoric acid) 40% vol. in kerosene presented the highest values for the distribution coefficient (D) for uranium. When synergistic systems were employed, the best results were obtained for DEHPA 40%vol. + PC88A 40%vol. and DEHPA 40% vol. + TOPO (trioctylphosphine oxide) 5% vol. in kerosene. 15% wt/v sodium carbonate was the best medium for uranium stripping and separation from iron, the main interfering element. Uranium was precipitated as sodium diuranate by adding sodium hydroxide (5,0 mol L -1 ). Thorium in the raffinate was extracted by TOPO (0,1% vol.) in cyclohexane. The radioactivity level of the final aqueous waste is similar to natural background, according to CNEN-NE 6.05 Norm. After neutralization, the solid can be co-processed, according to the Directory 264 from the National Brazilian Environmental Council (CONAMA), whereas the treated effluent can be discarded according to the Directory 357 from CONAMA. (author)

A study of using polythiol compounds and 2-ethyl-hexyl-acrylate with carbon tetrachloride as sensitizers for radiation vulcanization of natural rubber latex

International Nuclear Information System (INIS)

Polsuksiri, C.

1989-01-01

Experiments on using 3 different compounds of polythiol and an acrylate as sensitizer for radiation vulcanization were conducted. It was found that 1,4 butane diol propane tris-3-mercapto propionate showed the tendency to be a good sensitizer. The tensile strength of the rubber film prepared from the irradiated latex was found to be 14 MPa at sensitizer concentration of 1 phr and radiation dose of 45 kGy. As for 2-ethyl hexyl acrylate (2EHA), the maximum tensile strength of rubber film was found to be 23 MPa at concentration of 3 phr and radiation dose of 35 kGy. The mixture of 2 EHA and CCl 4 at various ratio was also used as sensitizer. The optimum ratio was found to be 5:1 at concentration of 6 phr and radiation dose of 15 kGy. The maximum tensile strength was as high as 25 MPa. The study also revealed that the radiation vulcanized latex with crosslink density of about 18x10 18 C.L./cm 3 would give the rubber film of highest tensile strength

Synthesis and Thermal Properties of Acrylonitrile/Butyl Acrylate/Fumaronitrile and Acrylonitrile/Ethyl Hexyl Acrylate/Fumaronitrile Terpolymers as a Potential Precursor for Carbon Fiber

OpenAIRE

Jamil, Siti Nurul Ain Md; Daik, Rusli; Ahmad, Ishak

2014-01-01

A synthesis of acrylonitrile (AN)/butyl acrylate (BA)/fumaronitrile (FN) and AN/EHA (ethyl hexyl acrylate)/FN terpolymers was carried out by redox polymerization using sodium bisulfite (SBS) and potassium persulphate (KPS) as initiator at 40 °C. The effect of comonomers, BA and EHA and termonomer, FN on the glass transition temperature (Tg) and stabilization temperature was studied using Differential Scanning Calorimetry (DSC). The degradation behavior and char yield were obtained by Thermog...

Method of isolation of traces of americium by using the +6 oxidation state properties

International Nuclear Information System (INIS)

Kwinta, Jean; Michel, Jean-Jacques

1969-05-01

The authors present a method to separate traces of americium from a solution containing fission products and actinides. This method comprises the following steps: firstly, the oxidation of americium at the +6 state by ammonium persulfate and carrying over of actinides and III and IV lanthanides by lanthanum fluoride; secondly, the reduction by hydrazine of the oxidized americium and carrying over of the reduced americium by lutetium fluoride; and thirdly, the americium-lutetium separation by selective extractions either with di 2 ethyl hexyl phosphoric acid, or by fractionated elution on an anionic resin column by a mixture of nitric acid and methanol [fr

Ultrasonic velocities, densities, and excess molar volumes of binary mixtures of N,N-dimethyl formamide with methyl acrylate, or ethyl acrylate, or butyl acrylate, or 2-ethyl hexyl acrylate at T = 308.15 K

Energy Technology Data Exchange (ETDEWEB)

Kondaiah, M. [Department of Physics, Acharya Nagarjuna University, Nagarjuna Nagar 522510, Andhra Pradesh (India); Sravana Kumar, D. [Dr. V.S. Krishna Govt. Degree College, Visakhapatnam, Andhra Pradesh (India); Sreekanth, K. [Department of Physics, Acharya Nagarjuna University, Nagarjuna Nagar 522510, Andhra Pradesh (India); Krishna Rao, D., E-mail: krdhanekula@yahoo.co.in [Department of Physics, Acharya Nagarjuna University, Nagarjuna Nagar 522510, Andhra Pradesh (India)

2011-12-15

Highlights: > Positive values of V{sub m}{sup E}, indicate dispersion forces between acrylic esters and DMF. > V{sub m}{sup E} values compared with Redlich-Kister polynomial. > Partial molar volumes data conclude that weak interactions exist in the systems. > Measured velocity values compared with theoretical values obtained by polynomials. - Abstract: Ultrasonic velocities, u, densities, {rho}, of binary mixtures of N,N-dimethyl formamide (DMF) with methyl acrylate (MA), ethyl acrylate (EA), butyl acrylate (BA), and 2-ethyl hexyl acrylate (EHA), including pure liquids, over the entire composition range have been measured at T = 308.15 K. Using the experimental results, the excess molar volume, V{sub m}{sup E}, partial molar volumes, V-bar {sub m,1}, V-bar{sub m,2}, and excess partial molar volumes, V-bar{sub m,1}{sup E}, V-bar{sub m,2}{sup E} have been calculated. Molecular interactions in the systems have been studied in the light of variation of excess values of calculated properties. The excess properties have been fitted to Redlich-Kister type polynomial and the corresponding standard deviations have been calculated. The positive values of V{sub m}{sup E} indicate the presence of dispersion forces between the DMF and acrylic ester molecules. Further theoretical values of sound velocity in the mixtures have been evaluated using various theories and have been compared with experimental sound velocities to verify the applicability of such theories to the systems studied. Theoretical ultrasonic velocity data have been used to study molecular interactions in the binary systems investigated.

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

International Nuclear Information System (INIS)

Arnold, W.D. Jr.

1977-01-01

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

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

OpenAIRE

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

2014-01-01

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

Recovery of uranium as a by product of phosphorites from Brazilian northeast area

International Nuclear Information System (INIS)

Gonzaga, M.; Abrao, A.

1976-01-01

The extraction and recobery of uranium contained in marine phosphates of northeast Brazil were investigated by treating ores with hydrochloric acid. The average content of uranium in the ore was found to be about 0,03 percent which corresponds to the highest worldly known content of uranium in phoshorite. The solutions obtained in laboratory, by leaching the phosphorite with hydrochloric acid, contained 40-70mg U/1. A method to control the uranium solubilization was outlined. A liquid-liquid extrction of uranium from these liquors was performed using a mixture of 3 percent di (2-ethyl hexyl)-phosphoric acid and 2.2 percent TBP in Kerosene. An overall uranium recovery of about 85 percent was reached

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

International Nuclear Information System (INIS)

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

2004-10-01

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

Study for uranium advantage as byproduct of the phosphorite from Brazilian Northeast

International Nuclear Information System (INIS)

Almeida, M.G. de.

1974-01-01

The distribution and recovery of uranium contained in marine phosphates from Northeast Brazil were investigated by treating these ores with hydrochloric acid. The average content of uranium in the phosphorite was found to be about 0.03%. The leaching of phosphate from the ore and the amount of solubilized uranium supplied the basic information for the uranium recovery. The solutions, obtained in laboratory, leaching the phosphorite with hydrochloric acid contained 40.70 mg:U/l. An analytical method to control the uranium solubilization was outlined. A liquid-liquid extraction of uranium from these leaching solutions was performed using mixture of 3.3% di-(2-ethyl-hexyl)-phosphoric acid and 2.2% TBP in kerosene. After extraction the phosphoric acid free from uranium is sent to the calcium hydrogeno-phosphate production. The uranium is stripped from the organic phase by alkaline treatment and then precipitated as diuranate. (Author) [pt

Electrochromic properties of multicolored novel polymer synthesized via combination of benzotriazole and N-functionalized 2,5-di(2-thienyl)-1H-pyrrole units

International Nuclear Information System (INIS)

Rende, Eda; Kilic, Cihan E.; Udum, Yasemin Arslan; Toffoli, Daniele; Toppare, Levent

2014-01-01

Synthesis of new conducting polymers is desired since their electrochemical and optical properties enable them to be used as active layers in many device applications. Benzotriazole and N-functionalized 2,5-di(2-thienyl)-1H-pyrrole (SNS Series) containing polymers showed very promising results as electrochromic materials. In order to observe the effect of the combination of these two units, three new monomers; 2-(6-(2,5-bis(5-methylthiophen-2-yl)-1H-pyrrol-1-yl)hexyl)-4,7-di (thiophen-2-yl)-2H benzo[d][1,2,3]triazole (M1), 2-(6-(2,5-di(thiophen-2-yl)-1H-pyrrol-1-yl)hexyl)-4,7-di(thiophen-2-yl) -2H-benzo[d][1,2,3]triazole (M2) and 2-(6-(2,5-di(thiophen-2-yl)-1H-pyrrol-1-yl)hexyl)-4,7-bis (5-methylthiophen-2-yl)-2H-benzo[d][1,2,3]triazole (M3) were synthesized. To better characterize the electronic and spectroscopic properties of the monomers, density functional theory (DFT) and its time-dependent generalization (TD-DFT) were used to calculate their vertical ionization potentials, vertical electron affinity and to simulate and interpret their infrared and UV-vis spectra. The monomers were electrochemically polymerized and the resultant polymers were characterized with cyclic voltammetry and UV-vis-NIR spectroscopy techniques. An electrochromic device was constructed with electrochemical polymer of M2. The device switched between red and blue colors and showed exceptional optical memory

Experimental and theoretical studies on the coordination chemistry of the N1-hexyl substituted pyrimidines (uracil, 5-fluorouracil and cytosine).

Science.gov (United States)

Barceló-Oliver, Miquel; Baquero, Beatriz Adriana; Bauzá, Antonio; García-Raso, Angel; Vich, Roberto; Mata, Ignasi; Molins, Elies; Terrón, Angel; Frontera, Antonio

2013-06-07

N(1)-Hexyl substituted pyrimidines were shown to present solubility properties closer to the real bases than the commonly used methyl and ethyl derivatives, yielding bi-layered structures in the solid state. The study of their coordination capabilities, mainly with Ag(I) and Hg(II), is presented in order to prove their reactivity. A series of coordination complexes, namely, [Hg(N(1)-hexyl-5-fluorouracilate)2]4·6H2O (1), (Ag(+))·[Ag(N(1)-hexyl-5-fluorouracilate)2](-) (2), [Ag(NO3)(N(1)-hexyluracil-κO(4))4] (3), [ZnBr2(N(1)-hexylcytosine)2] (4), [CdBr2(N(1)-hexylcytosine)2] (5), [HgBr2(N(1)-hexylcytosine)2] (6) and [CoBr2(N(1)-hexylcytosine)2] (7), have been synthesized in good yields and X-ray characterized. The presence of the hexyl chains and the fluorine atoms causes the formation of interesting 3D architectures in the solid state. Their structures have been further characterized by infrared spectra (IR) and elemental analyses. In addition, DFT-D3 calculations are used to study interesting noncovalent interactions observed in the solid state, like fluorine-fluorine, fluorine-π and hydrophobic interactions.

Towards zero discharge by integrated effluent treatment approach

International Nuclear Information System (INIS)

Rath, Ashish Kumar; Pattnaik, Sambhu Prasad; Pati, Ganeswar; Saha, Sushant; Viswanath, Kowtha

2014-01-01

Heavy Water Plant, Talcher houses two Organo-phosphorus Solvent Production Plants namely, 60 MTPY TBP Plant engaged in the production of Tri-n-Butyl Phosphate and Versatile Solvent Production Plant (VSPP) capable of producing various Organo Phosphorus Solvents namely, 100 MTPY D2EHPA (Di-2-Ethyl Hexyl Phosphoric Acid), or 40 MTPY TAPO (Tri-Alkyl Phosphine Oxide) or TOPO (Tri-n-Octyl Phosphine Oxide) or DNPPA (Di-Nonyl Phenyl Phosphoric Acid). These solvents have important application for separation duties in front and back end of nuclear fuel cycle and also in conventional hydrometallurgy for separation metals like Ni, Cu, Zn, Co etc., both of these plants are first of their kind in India designed by the Heavy Water Board, Mumbai with R and D inputs from BARC. The two plants employ esterification (1) process between PCl 3 / and a suitable oxo-alcohol followed by hydrolysis, neutralization and product purification. The second and third steps find large usage of Water, which eventually surface as liquid effluent. All the gaseous emissions from plants, mostly HCl gas are traded off for Saline Water as liquid effluent by scrubbing the same with Sodium Hydroxide Solution

Production of gadolinium nitrate for TAPS 3 and 4 PHWR

International Nuclear Information System (INIS)

Mishra, S.L.; Ramakrishnan, P.; Iyer, N.S.; Singh, Harvinderpal

2004-01-01

In India, gadolinium nitrate is being used for the first time in PHWR at Tarapur. Gadolinium is preferred over boron due to high neutron cross section and the water soluble nitrate form works efficiently for reactivity control through moderator liquid poison addition system (MLPS) as well as for reactor shut down system (SDS2). Low concentration of gadolinium (0.1-0.2 g/l) in heavy water is sufficient to shut down the reactor in a very short time. After use, the small amount of gadolinium can be separated quickly from heavy water by ion exchange process. In this paper separation of Gd using of 2-ethyl hexyl phosphoric acid mono 2-ethyl hexyl ester EHEHPA as an extractant has been described

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

International Nuclear Information System (INIS)

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

2009-01-01

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

100 keV 10-B+ implantation into poly-(di-n-hexyl silane), (PDHSi)

International Nuclear Information System (INIS)

Fink, D.; Mueller, M.; Behar, M.; Papaleo, R.M.

2006-01-01

100 keV 10 B + ions were implanted into poly-(di-n-hexyl silane) in different directions at a fluence of 1 x 10 14 cm -2 , and their depth distribution was determined by means of the neutron depth profiling technique. In no case were the projectile ions found to come to rest according to their predicted range profiles. Instead, they are always found to undergo considerable long-range migration. During the irradiation process this motion appears to be radiation-enhanced, and during the subsequent annealing steps one appears to deal with regular thermal diffusion. The implant redistribution is always found to be governed strongly by the self-created damage, insofar as both electronic and nuclear defects in the polymer act as trapping centers. Their population ratio is modified by thermal annealing. The as-implanted redistribution shows a pronounced directional dependence, which essentially is a consequence of the spatial distributions of the electronic and nuclear damage. The changes of the nuclear defect distribution during thermal annealing are studied by a specially developed tomographic method. It is found that boron is preferentially trapped along the irradiation direction, exhibiting quite pronounced prolate (i.e. cigar-like) distributions. This shape is almost unaffected by thermal annealing. (orig.)

Liquid–liquid equilibria study of the (water + phosphoric acid + hexyl or cyclohexyl acetate) systems at T = (298.15, 308.15, and 318.15) K: Measurement and thermodynamic modelling

International Nuclear Information System (INIS)

Ghanadzadeh Gilani, A.; Ghanadzadeh Gilani, H.; Shekarsaraee, S.; Nasiri-Touli, E.; Seyed Saadat, S.L.

2016-01-01

Highlights: • Tie line data for aqueous solutions of phosphoric acid with esters were obtained. • The LLE data were correlated using the UNIQUAC and NRTL models. • The quality of the LLE data was validated using the appropriate equations. • Separation factors were calculated for the chosen solvents. - Abstract: Liquid–liquid equilibrium (LLE) data for the (water + phosphoric acid + n-hexyl acetate or cyclohexyl acetate) ternary systems were determined at T = (298.15, 308.15 and 318.15) K and p = 101.3 kPa. The cloud point method was used to obtain the solubility and the Karl-Fischer, acidimetric titration, and refractive index methods were used to determine the tie-line values. Both the ternary systems exhibit type-1 behavior of LLE. The experimental values were regressed and acceptably correlated using the UNIQUAC and NRTL models. The reliability of the experimental tie lines was confirmed using the Othmer–Tobias plot. Experimental distribution coefficients and separation factors were fitted using the Kamlet–Taft LSER model. The influence of temperature on the biphasic area and separation factor was found to be minor. As a result, both the esters are suitable separating agents for aqueous phosphoric acid mixtures.

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

Science.gov (United States)

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

2014-01-01

The reaction of (di­methyl­phosphor­yl)methanamine (dpma) with oxalic acid in ethanol yielded the title solvated salt, C3H11NOP+·C2HO4 −·0.5C2H2O4. Its asymmetric unit consists of one dpmaH+ cation, one hydrogen oxalate anion and a half-mol­ecule of oxalic acid located around a twofold rotation axis. The H atom of the hydrogen oxalate anion is statistically disordered over two positions that are trans to each other. The hydrogen oxalate monoanion is not planar (bend angle ∼16°) whereas the oxalic acid molecule shows a significantly smaller bend angle (∼7°). In the crystal, the components are connected by strong O—H⋯O and much weaker N—H⋯O hydrogen bonds, leading to the formation of layers extending parallel to (001). The structure was refined from a racemically twinned crystal with twin components in an approximate 1:1 ratio. PMID:24765013

Effect of the Side Chains and Anode Material on Thermal Stability and Performance of Bulk-Heterojunction Solar Cells Using DPP(TBFu2 Derivatives as Donor Materials

Directory of Open Access Journals (Sweden)

Alexander Kovalenko

2015-01-01

Full Text Available An optimized fabrication of bulk-heterojunction solar cells (BHJ SCs based on previously reported diketopyrrolopyrrole donor, ethyl-hexylated DPP(TBFu2, as well as two new DPP(TBFu2 derivatives with ethyl-hexyl acetate and diethyl acetal solubilizing side-chains and PC60BM as an acceptor is demonstrated. Slow gradual annealing of the solar cell causing the effective donor-acceptor reorganization, and as a result higher power conversion efficiency (PCE, is described. By replacing a hole transporting layer PEDOT:PSS with MoO3 we obtained higher PCE values as well as higher thermal stability of the anode contact interface. DPP(TBFu2 derivative containing ethyl-hexyl acetate solubilizing side-chains possessed the best as-cast self-assembly and high crystallinity. However, the presence of ethyl-hexyl acetate and diethyl acetal electrophilic side-chains stabilizes HOMO energy of isolated DPP(TBFu2 donors with respect to the ethyl-hexylated one, according to cyclic voltammetry.

Features of the Thermodynamics of Trivalent Lanthanide/Actinide Distribution Reactions by Tri-n-Octylphosphine Oxide and Bis(2-EthylHexyl) Phosphoric Acid

Energy Technology Data Exchange (ETDEWEB)

Travis S. Grimes; Peter R. Zalupski

2014-11-01

A new methodology has been developed to study the thermochemical features of the biphasic transfer reactions of trisnitrato complexes of lanthanides and americium by a mono-functional solvating ligand (tri-n-octyl phosphine oxide - TOPO). Stability constants for successive nitrato complexes (M(NO3)x3-x (aq) where M is Eu3+, Am3+ or Cm3+) were determined to assist in the calculation of the extraction constant, Kex, for the metal ions under study. Enthalpies of extraction (?Hextr) for the lanthanide series (excluding Pm3+) and Am3+ by TOPO have been measured using isothermal titration calorimetry. The observed ?Hextr were found to be constant at ~29 kJ mol-1across the series from La3+-Er3+, with a slight decrease observed from Tm3+-Lu3+. These heats were found to be consistent with enthalpies determined using van ’t Hoff analysis of temperature dependent extraction studies. A complete set of thermodynamic parameters (?G, ?H, ?S) was calculated for Eu(NO3)3, Am(NO3)3 and Cm(NO3)3 extraction by TOPO and Am3+ and Cm3+ extraction by bis(2-ethylhexyl) phosphoric acid (HDEHP). A discussion comparing the energetics of these systems is offered. The measured biphasic extraction heats for the transplutonium elements, ?Hextr, presented in these studies are the first ever direct measurements offered using two-phase calorimetric techniques.

Radiochemical studies in chemical separation and spectrographic determination of rare earths in thorium oxide matrix (Preprint No. RA.06)

International Nuclear Information System (INIS)

Adya, V.C.; Dhawale, B.A.; Rajeshwari, B.; Bangia, T.R.; Sastry, M.D.

1989-01-01

A chemical separation procedure was standardised for the separation of traces of rare earths from ThO 2 matrix using HDEHP (Di 2-ethyl hexyl phosphoric acid). The studies were carried out using both nitric acid and hydrochloric acid medium in different concentrations. The extraction studies were also carried out using radioactive isotopes of rare earths viz. 141 Ce, 152-154 Eu, 153 Gd, 170 Tm etc. The extraction was effective in both media. In 0.1 M HDEHP/xylene and 3 M HNO 3 , Ce was partially extracted into organic phase. So HCl/xylene medium was chosen for extraction purposes. The recovery was confirmed by both gamma counting and emission spectropgraphic method. It was found to be quantitative within experimental error. The separation procedure development here was used for determination of rare earths in thorium oxide matrix by emission spectrographic method. (author)

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

Energy Technology Data Exchange (ETDEWEB)

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

2017-07-01

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

Study on selective separation of uranium(VI) by new N,N-dialkyl carboxy-amides

International Nuclear Information System (INIS)

Suzuki, Shinichi; Sugo, Yumi; Kimura, Takaumi; Yaita, Tsuyoshi

2007-01-01

-amides and group separation of Pu-Np linear alkyl type N,N-di-alkyl carboxy-amide for FBR and LWR spent fuel treatment. Since the branched alkyl type N,N-di-alkyl carboxy-amides have the steric hindrance on the complexation with metal cations, branched alkyl type N,N-di-alkyl carboxy-amides can be used to separate An(VI) from An(IV). On the other hand, linear type N,N-di-alkyl carboxy-amides have potential for alternative extractant for tri-butyl phosphate(TBP) because linear type N,N-di-alkyl-amide can extract An(VI) and An(IV). In our previous research work, we have proposed N,N-di-(2- ethyl)hexyl-(2,2-dimethyl)-propanamide (D2EHDMPA) as a candidate extractant for uranium selective separation in FBR spent fuel treatments. However D2EHDMPA was able to separate uranium(VI) from plutonium(IV) and neptunium(VI), D2EHDMPA showed poor U(VI) loading capacity in organic phase. For the purpose of improvement of U(VI) loading capacity in organic phase, nineteenth kinds of New N,N-di-alkyl-amides: N,N-di-hexyl-(3,3-dimethyl)butanamide (DHDMBA), N,N-di-oxyl-(3,3-dimethyl)butanamide (DODMBA), N,N-di-hexyl-(2,2-dimethyl)propanamide (DHDMPA) N,N-di-octyl-(2,2-dimethyl)propanamide (DODMPA), N,N-di-octyl-(2-ethyl)butanamide (DO2EBA), N,N-di-hexyl-(2-ethyl)butanamide (DH2EBA), N-benzyl-N-R 1 -(2-ethyl)hexanamide (R 1 :- C 4 H 9 , -C 6 H 13 , -C 8 H 17 , N-cyclohexyl-N-R 1 -(2- ethyl)hexanamide (R 1 :-C 4 H 9 , -C 6 H 13 , -C 8 H 17 ), N-phenyl- N-R 1 -(2-ethyl)hexanamide (R 1 :-C 3 H 9 , -C 4 H 9 , -C 5 H 11 , - C 6 H 13 , -C 8 H 17 , N-(2-ethyl)hexyl-N-Phenyl-octanamide, N-Benzyl- N-Phenyl-(2-ethyl)hexanamide are synthesized. In this paper, our experimental results of new N,N-dialkyl carboxy-amides extraction property of U(VI)/Pu(IV), extraction of macro amount of U(VI), and gamma-ray radiolysis will be summarized. Solvent extraction of U(VI) and Pu (IV) by nineteenth kinds of new N,N-di-alkyl carboxy-amides, macro amount of U(VI) extraction and radiolysis of four compounds were carried

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

International Nuclear Information System (INIS)

Kraikaew, Jarunee; Srinuttakul, Wanee

2004-01-01

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

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

International Nuclear Information System (INIS)

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

2017-01-01

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

Pseudosymmetric fac-di-aqua-trichlorido[(di-methyl-phosphor-yl)methanaminium-κO]manganese(II).

Science.gov (United States)

Reiss, Guido J

2013-05-01

In the title compound, [Mn(C3H11NOP)Cl3(H2O)2], the Mn(II) metal center has a distorted o-cta-hedral geometry, coordinated by the three chloride ligands showing a facial arrangement. Two water mol-ecules and the O-coordinated dpmaH cation [dpmaH = (di-methyl-phosphor-yl)methanaminium] complete the coordination sphere. Each complex mol-ecule is connected to its neighbours by O-H⋯Cl and N-H⋯Cl hydrogen bonds. Two of the chloride ligands and the two water ligands form a hydrogen-bonded polymeric sheet in the ab plane. Furthermore, these planes are connected to adjacent planes by hydrogen bonds from the aminium function of cationic dpmaH ligand. A pseudo-mirror plane perpendicular to the b axis in the chiral space group P21 is observed together with inversion twinning [ratio = 0.864 (5):0.136 (5)].

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

International Nuclear Information System (INIS)

Chaudry, M.A.; Ahmad, I.

2000-01-01

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

Synthesis and Antimicrobial Activity of Novel Substituted Ethyl 2-(Quinolin-4-yl-propanoates

Directory of Open Access Journals (Sweden)

Yong Zhou

2013-03-01

Full Text Available Substituted 4-hydroxyquinolines were synthesized from anilines and diethyl 2-(ethoxymethylenemalonate by the Gould-Jacobs reaction via cyclization of the intermediate anilinomethylenemalonate followed by hydrolysis and decarboxylation. The 4-hydroxyquinolines reacted with phosphorous oxychloride to form 4-chloroquinolines, which reacted on heating with diethyl sodiomethylmalonate in DMF to yield moderate yields of substituted ethyl 2-(quinolin-4-ylpropanoates, many of which showed potent antimicrobial activity against Helicobacter pylori.

Studies on supercritical fluid extraction of uranium from sodium diuranate

International Nuclear Information System (INIS)

Prabhat, Parimal; Vithal, G.K.; Rao, Ankita; Kumar, Pradeep; Tomar, B.S.

2014-01-01

Crude sodium diuranate (SDU) produced from phosphoric acid by solvent extraction process with di-2-ethyl hexyl phosphoric acid (D2EHPA) and tri-n-butyl phosphate(TBP) contains iron and other rare earth impurities along with uranium. For further use of this uranium for fuel fabrication and its subsequent use in nuclear reactors, it has to be purified up to nuclear grade ammonium diuranate (ADU) specifications. Conventionally crude SDU is being purified by dissolving it in nitric acid followed by solvent extraction process using TBP in diluent. Use of large amount of acid and organic solvents for industrial processes is an environmental concern. Nowadays there are efforts to minimize use of acid and organic solvents in industrial processes. Supercritical Fluid Extraction (SFE) of uranium from different matrices (solid as well as liquid) has been reported by several authors in recent years. Near complete extraction of uranium from UO 2 (powder, green pellet and sintered pellet) using TBP-HNO 3 adduct by SFE has been reported. We attempted to explore possibility to purify crude SDU to nuclear grade by SFE of uranium from crude SDU matrix and study the effect of different operational parameters, mode of extraction and complexation

A contribution to the study of the extraction of mineral acids and of actinide (IV) and (VI) cations by N,N-dialkylamides

International Nuclear Information System (INIS)

Condamines, N.

1990-03-01

N,N-dialkylamides are alternate extractants to tributylphosphate, TBP, for the actinides separation in nuclear fuel reprocessing. N,N-di (2-ethyl hexyl) butyramide and N,N-di (2 ethyl hexyl) isobutyramide are selected for their sufficient extraction and partition ability towards actinides (IV) and (VI) without coextracting fission products. Mechanisms of HNO 3 , UO 2 2+ , Pu 4+ , Th 4+ are investigated. Nitric acid extraction is due to the competitive formation of the species (HNO 3 )L 2 , (HNO 3 )L, (HNO 3 ) 2 L (L: DOBA or DOiBA). An hydrogen bond is the driving force of the transfer. For low acidity media, amides are neutral extractants. Physical interactions, between free ligand and metallic complex, arise for high amide concentrations. Taking into account the non-ideality of the organic medium by a hard spheres mixture model, we estimate that such interactions are far from negligible and very specific to the amide group. Unlike TBP, when increasing acidity, amides behave as anionic extractants. DOBA and DOiBA appear to be satisfactory extractants for fuel reprocessing [fr

(Vapour + liquid) equilibria, volumetric and compressibility behaviour of binary and ternary aqueous solutions of 1-hexyl-3-methylimidazolium chloride, methyl potassium malonate, and ethyl potassium malonate

International Nuclear Information System (INIS)

Sadeghi, Rahmat; Mahdavi, Adibeh

2012-01-01

Highlights: ► VLE and volumetry of binary and ternary [C 6 mim][Cl], MPM and EPM aqueous solutions. ► Constant a w lines show small negative deviation from the linear isopiestic relation. ► Solute–water interactions follow the order: EPM > MPM > [C 6 mim][Cl]. ► MPM and EPM have a very weak salting-out effect on [C 6 mim][Cl] aqueous solutions. - Abstract: (Vapour + liquid) equilibrium data (water activity, vapour pressure, osmotic coefficient, and activity coefficient) of binary aqueous solutions of 1-hexyl-3-methylimidazolium chloride ([C 6 mim][Cl]), methyl potassium malonate, and ethyl potassium malonate and ternary {[C 6 mim][Cl] + methyl potassium malonate} and {[C 6 mim][Cl] + ethyl potassium malonate} aqueous solutions were obtained through the isopiestic method at T = 298.15 K. These results reveal that the ionic liquid behaves as surfactant-like and aggregates in aqueous solutions at molality about 0.4 mol · kg −1 . The constant water activity lines of all the ternary systems investigated show small negative deviations from the linear isopiestic relation (Zdanovskii–Stokes–Robinson rule) derived using the semi-ideal hydration model. The density and speed of sound measurements were carried out on solutions of methyl potassium malonate and ethyl potassium malonate in water and of [C 6 mim][Cl] in aqueous solutions of 0.25 mol · kg −1 methyl potassium malonate and ethyl potassium malonate at T = (288.15 to 308.15) K at atmospheric pressure. From the experimental density and speed of sound data, the values of the apparent molar volume, apparent molar isentropic compressibility and excess molar volume were evaluated and from which the infinite dilution apparent molar volume and infinite dilution apparent molar isentropic compressibility were calculated at each temperature. Although, there are no clear differences between the values of the apparent molar volume of [C 6 mim][Cl] in pure water and in methyl potassium malonate or ethyl

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

Science.gov (United States)

Sahu, Ishwar Prasad

2016-08-01

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

Study on the interactions PVC/plasticizers by NMR

Energy Technology Data Exchange (ETDEWEB)

Tavares, Maria I.B.; Monteiro, Elisabeth E.C. [Universidade Federal, Rio de Janeiro, RJ (Brazil). Inst. de Macromoleculas; Harris, Robin [Durham Univ. (United Kingdom). Dept. of Chemistry

1992-12-31

The nature of the interactions between PVC and plasticizers as di-butyl phthalate and di-2-ethyl-hexyl phthalate can be investigated using proton/carbon-13 NMR techniques. The measurements of T{sub 1} for protons and carbon-13 and T{sub 1} P for protons can provide a good source of information about the complex behaviour for those two systems which were investigated. (author) 14 refs., 5 figs., 1 tab.

40 CFR 721.10088 - Thiophene, 2,5-dibromo-3-hexyl-.

Science.gov (United States)

2010-07-01

..., and consumer activities. Requirements as specified in § 721.80(s) (4,500 kilograms). (ii) Release to... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Thiophene, 2,5-dibromo-3-hexyl-. 721.10088 Section 721.10088 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED) TOXIC...

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

International Nuclear Information System (INIS)

Abdel-Khalek, A.A.

2011-01-01

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

Application of liquid-liquid extraction in separation of rare earths [Paper No. : V-6

International Nuclear Information System (INIS)

Deshpande, S.M.; Krishnan, N.P.K.; Murthy, T.K.S.; Swaminathan, T.V.

1979-01-01

The rare earths consist of fifteen elements which have very similar chemical properties and are difficult to separate from each other. Since they exist together in all naturally occurring minerals their separation is one of the important and difficult aspects of their technology. Liquid-liquid extraction has proved to be an efficient technique for their separation. The two important extraction systems that find practical and large scale application, the nitric acid + tri-n-butyl phosphate, and mineral acid (particularly hydrochloric acid) + organo phosphoric acid (like di-2-ethyl hexyl phosphoric acid), are briefly reviewed. The factors affecting the extraction and separation of rare earths in the two systems are discussed. On an industrial scale the extraction process is very often employed for an initial concentration of the desired rare earths from complex mixtures. The final purification is generally achieved by the ion exchange method. The utility of the solvent extraction process for the upgrading of selected rare earths-europium, samarium and gadolinium-from a mixed rare earth chloride, derived from monazite, is illustrated by the work carried out in this laboratory and pilot plant operation at the Alwaye plant of M/s. Indian Rare Earths Ltd. (author)

The Effect of Time dealumination and Solvent Concentration in Synthesis of Zeolite Catalyst and Catalytic Test for DiEthyl Ether Production Process

International Nuclear Information System (INIS)

Widayat; Roesyadi, A.; Rachimoellah, M.

2009-01-01

Ethanol is an alternative energy, but its has three distinct disadvantages as a transportation fuel. Its availability is currently limited, and it has a lower volumetric heating value and a lower Reid vapour pressure (RVP) than gasoline. This paper focuses for this disadvantages and to solve this problem can do with converts ethanol to DiEthyl Ether product. This research produced DiEthyl Ether by ethanol dehydration process with zeolite as catalyst. The catalyst synthesis from natural material from District Gunung Kidul, Indonesia. The catalyst produced with dealumination, neutralization, drying and calcination processes. The zeolite catalyst was analysed of Si/Al, X-ray Diffraction and specific surface area. The catalyst product then used for ethanol dehydration to produce DiEthyl Ether. The results shown the biggest surface area is 184,52 m 2 /gram at catalyst production at 10 hours for time dealumination. The crystallite of catalyst product is similar like shown at diffractogram of XRD analysis. The ratio Si/Al biggest is 313.7 that obtaining at catalyst production with 7 hours for time dealumination. The catalytic test use fixed bed reactor with 1 inci diameter and ethanol fermentation both as feed. The operation condition is 150 deg. C at temperature and atmosphere pressure. The compounds product in liquid phase are diethyl ether, methanol and water.

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

International Nuclear Information System (INIS)

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

1995-09-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2017-03-15

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

A contribution to the study of the extraction of mineral acids and of actinide (IV) and (VI) cations by N,N-dialkylamides; Contribution a l'etude de l'extraction d'acides mineraux et de cations actinides aux degres d'oxydation (IV) et (VI) par des N,N-dialkylamides

Energy Technology Data Exchange (ETDEWEB)

Condamines, N

1990-03-15

N,N-dialkylamides are alternate extractants to tributylphosphate, TBP, for the actinides separation in nuclear fuel reprocessing. N,N-di (2-ethyl hexyl) butyramide and N,N-di (2 ethyl hexyl) isobutyramide are selected for their sufficient extraction and partition ability towards actinides (IV) and (VI) without coextracting fission products. Mechanisms of HNO{sub 3}, UO{sub 2}{sup 2+}, Pu{sup 4+}, Th{sup 4+} are investigated. Nitric acid extraction is due to the competitive formation of the species (HNO{sub 3})L{sub 2}, (HNO{sub 3})L, (HNO{sub 3}){sub 2}L (L: DOBA or DOiBA). An hydrogen bond is the driving force of the transfer. For low acidity media, amides are neutral extractants. Physical interactions, between free ligand and metallic complex, arise for high amide concentrations. Taking into account the non-ideality of the organic medium by a hard spheres mixture model, we estimate that such interactions are far from negligible and very specific to the amide group. Unlike TBP, when increasing acidity, amides behave as anionic extractants. DOBA and DOiBA appear to be satisfactory extractants for fuel reprocessing.

Application of the radiochemical - and the direct gamma ray spectrometry method to the burnup determination of irradiated uranium oxide

International Nuclear Information System (INIS)

Cunha, I.I.L.

1979-01-01

The burn up of natural U 3 O 8 that occurs by the action of thermal neutrons was determined, using the radioisotopes 144 Ce, 137 Cs, 103 Ru, 106 Ru and 95 Zr as monitors. The determination of the burn up was made using both destructive and non-destructive methods. In the non-destructive method, the technique of direct gamma-ray spectrometry was used and the radioisotopes mentioned were simultaneously counted in a Ge-Li detector. In the radiochemical method the same radioisotopes were isolated one from the other and from all other fission products before counting. The solvent extraction technique was used for the radiochemical separation of uranium, cerium, cesium and ruthenium. To separate zirconium and niobium, adsorption in silica-gel was used. The extraction agent employed to isolate cesium was dipycrilamine and for the separation of the other radioisotopes Di-(2-Ethyl Hexyl) Phosphoric acid (HDEHP) was used. (Author) [pt

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

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

International Nuclear Information System (INIS)

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

2005-01-01

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

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

International Nuclear Information System (INIS)

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

2009-01-01

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

Y{sub 2}O{sub 3}: Dy{sup 3+}/Li{sup +} phosphors synthesized by spray

Energy Technology Data Exchange (ETDEWEB)

Balderas X, R.; Carmona T, S.; Falcony, C., E-mail: scarmonat81@gmail.com [IPN, Centro de Investigacion y de Estudios Avanzados, Apdo. Postal 14-740, 07000 Ciudad de Mexico (Mexico)

2017-11-01

Dysprosium and lithium-activated yttrium oxide phosphor was synthesized at 1100 degrees Celsius by ultrasonic spray pyrolysis (Usp) using Di water as solvent and metal chlorides as precursors. The characteristic emission peak of Dy{sup 3+} due to the transitions {sup 4}F{sub 9/2} to {sup 6}H{sub 15/2} at 483 nm, {sup 4}F{sub 9/2} to {sup 6}H{sub 13/2} at 573 nm, {sup 4}F{sub 9/2} to {sup 6}H{sub 11/2} at 667 nm and {sup 4}F{sub 9/2} to {sup 6}H{sub 9/2} at 766 nm were observed. Scanning electron microscopy and transmission electron microscopy measurements were carried out to understand surface morphological features and the particle size of the phosphor. The uniformity of phase of Dy{sup 3+} - Li{sup +} doped Y{sub 2}O{sub 3} phosphors was checked by X-ray diffraction technique. The phosphors form clusters that were found to be ∼ 1 μm in size, however, particles that form these clusters have sizes between 40 and 120 nm. (Author)

Luminescence properties of cerium-doped di-strontium magnesium di-silicate phosphor by the solid-state reaction method

Science.gov (United States)

Prasad Sahu, Ishwar

2016-05-01

A series of Sr2MgSi2O7:xCe3+ (x = 1.0%, 2.0%, 3.0%, 4.0% and 5.0%) phosphors were synthesized by the solid-state reaction method. The phosphor with optimum thermoluminescence, photoluminescence and mechanoluminescence (ML) intensity was characterized by X-ray diffraction, field emission scanning electron microscopy, energy-dispersive X-ray spectroscopy and Fourier transform infrared techniques. The trapping parameters (i.e. activation energy, frequency factor and order of the kinetics) of each synthesized phosphor have been calculated using the peak shape method and the results have been discussed. Under ultraviolet excitation (325 nm), Sr2MgSi2O7:xCe3+ phosphors were composed of a broad band peaking at 385 nm, belonging to the broad emission band which emits violet-blue color. Commission International de I'Eclairage coordinates have been calculated for each sample and their overall emission is near violet-blue light. In order to investigate the suitability of the samples for industrial uses, color purity and color rendering index were calculated. An ML intensity of optimum [Sr2MgSi2O7:Ce3+ (3.0%)] phosphor increases linearly with increasing impact velocity of the moving piston which suggests that these phosphors can be used as fracto-ML-based devices. The time of the peak ML intensity and the decay rate did not change significantly with respect to increasing impact velocity of the moving piston.

A tentative characterization of volatile compounds from Iberian Dry-Cured Ham according to different anatomical locations. A detailed study

Directory of Open Access Journals (Sweden)

Narváez-Rivas, Mónica

2010-12-01

Full Text Available The aim of this work was to carry out a characterization of the volatile fraction of 23 Iberian dry-cured hams by GC-iontrap- MS. Two different locations –subcutaneous fat and musclefrom the slices taken parallel to the femur from each ham were analyzed. The analyses were done by Gas Chromatography- Mass Spectrometry with a polar capillary column and after a previous extraction using the Purge and Trap method. A total of 109 volatile compounds were identified, twenty-eight of which for the first time in Iberian dry-cured ham (isopropanol, 4-methyl-5-decanol, 2-butyl-1-octanol, 2-etoxy-ethanol, 2-ethyl-phenol, 2-hexen-1-ol, 3,5-octadien-2-ol, 2-decen- 1-ol, 5-ethylcyclopent-1-enecarboxaldehyde, 2,4-heptadienal, 6-nonenal, cyclopentanone, 3-ethenyl-cyclohexanone, 2-methyl-cyclopentanone, 6-octen-2-one, 5-methyl-2-(1-methylethyl- cyclopentanone, 3,5-octadien-2-one, 2-hydroxymethyl- 2,3,3-trimethyl-oxirane, 2-ethyl-hexyl 2-propenoate, 1-methoxypentane, 2,3-dihydrofurane, 2-D-2-pentadecyl-1,3-dioxolane, hexyl octyl eter, eucalyptol, di-(3-methyl-buthyl eter, piperidine, isopropylamine and 2-ethenyl-pyridine.

El objetivo de este trabajo fue llevar a cabo una caracterización de la fracción volátil de 23 jamones curados de cerdo ibérico mediante GC-ion-trap-MS. Se analizaron dos zonas diferentes de las lonchas tomadas paralelas al fémur de cada jamón, Grasa subcutánea y magro. El análisis se realizó mediante cromatografía gaseosa en columna capilar de alta polaridad con detección de espectrometría de masas y extracción previa de la fracción volátil mediante purga y trampa. Un total de 109 compuestos volátiles fueron identificados, veintiocho de ellos descritos por primera vez en Jamón ibérico curado (isopropanol, 4-methyl-5-decanol, 2-butyl-1-octanol, 2-etoxy-ethanol, 2-ethyl-phenol, 2-hexen-1-ol, 3,5-octadien-2- ol, 2-decen-1-ol, 5-ethylcyclopent-1-enecarboxaldehyde, 2,4-heptadienal, 6-nonenal, cyclopentanone, 3-ethenyl

Phthalate esters in main source water and drinking water of Zhejiang Province (China): Distribution and health risks.

Science.gov (United States)

Wang, Xiaofeng; Lou, Xiaoming; Zhang, Nianhua; Ding, Gangqiang; Chen, Zhijian; Xu, Peiwei; Wu, Lizhi; Cai, Jianmin; Han, Jianlong; Qiu, Xueting

2015-10-01

To evaluate the distributions and health risks of phthalate esters in the main source water and corresponding drinking water of Zhejiang Province, the concentrations of 16 phthalate esters in water samples from 19 sites were measured from samples taken in the dry season and wet season. The concentration of the total phthalate ester congeners in source water ranged from 1.07 μg/L to 7.12 μg/L in the wet season, from 0.01 μg/L to 1.58 μg/L in the dry season, from 1.18 μg/L to 15.28 μg/L from drinking water in the wet season, and from 0.16 μg/L to 1.86 μg/L from drinking water in the dry season. Of the 16 phthalate esters, dimethyl phthalate, dibutyl phthalate, di-(2-ethyl-hexyl) phthalate, di-iso-butyl phthalate, bis-2-n-butoxyethyl phthalate, and dicyclohexyl phthalate were present in the samples analyzed, dominated by di-iso-butyl phthalate and di-(2-ethyl-hexyl) phthalate. The concentrations of phthalate esters in the wet season were all relatively higher than those in the dry season, and the drinking water had higher concentrations of phthalate esters than source water. The phthalate ester congeners studied pose little health risk to nearby citizens. Environ Toxicol Chem 2015;34:2205-2212. © 2015 SETAC. © 2015 SETAC.

Pseudosymmetric fac-di­aqua­trichlorido[(di­methyl­phosphor­yl)methanaminium-κO]manganese(II)

Science.gov (United States)

Reiss, Guido J.

2013-01-01

In the title compound, [Mn(C3H11NOP)Cl3(H2O)2], the MnII metal center has a distorted o­cta­hedral geometry, coordinated by the three chloride ligands showing a facial arrangement. Two water mol­ecules and the O-coordinated dpmaH cation [dpmaH = (di­methyl­phosphor­yl)methanaminium] complete the coordination sphere. Each complex mol­ecule is connected to its neighbours by O—H⋯Cl and N—H⋯Cl hydrogen bonds. Two of the chloride ligands and the two water ligands form a hydrogen-bonded polymeric sheet in the ab plane. Furthermore, these planes are connected to adjacent planes by hydrogen bonds from the aminium function of cationic dpmaH ligand. A pseudo-mirror plane perpendicular to the b axis in the chiral space group P21 is observed together with inversion twinning [ratio = 0.864 (5):0.136 (5)]. PMID:23723764

Crystal structure of ethyl 2-(diethoxyphosphoryl-2-(2,3,4-trimethoxyphenylacetate

Directory of Open Access Journals (Sweden)

Moritz Schubert

2014-09-01

Full Text Available The title compound, C17H27O8P, was prepared by Michaelis–Arbuzov reaction of ethyl 2-bromo-2-(2,3,4-trimethoxyphenylacetate and triethyl phosphite. Such compounds rarely crystallize, but single crystals were recovered after the initial oil was left for approximately 10 years. The bond angle of the sp3-hybridized C atom connecting the benzene derivative with the phospho unit is widened marginally [112.5 (2°]. The terminal P—O bond length of 1.464 (2 Å clearly indicates a double bond, whereas the two O atoms of the ethoxy groups connected to the phosphorous atom have bond lengths of 1.580 (2 Å and 1.581 (3 Å. The three methoxy groups emerge out of the benzene-ring plane due to steric hindrance [C—C—O—C torsion angles = −179.9 (3°, −52.9 (4° and 115.3 (4°]. In the crystal, inversion dimers linked by pairs of C—H...O=P hydrogen bonds generate R22(14 loops. The chosen crystal was modelled as a non-merohedral twin.

Fetal Phthalate Screen: Assessment of Several Phthalate Esters on Fetal Rodent Testosterone Production and Gene Expression Following In Utero Exposure

Science.gov (United States)

Phthalate esters(PE) are a large family of compounds used in a wide array of common products from medical tubing to pharmaceuticals to cables, and wall/floor coverings. Laboratory studies have demonstrated that in utero treatment with PE such as di-ethyl hexyl phthalate (DEHP) du...

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

International Nuclear Information System (INIS)

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

2009-01-01

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

Phosphategypsum wastes in Venice lagoon. Radiological impact; Le discariche di fosfogessi nella laguna di Venezia. Valutazioni preliminari dell'impatto radiologico

Energy Technology Data Exchange (ETDEWEB)

Belli, M; Blasi, M; Guogang, J.; Rosamilia, S.; Sansone, U. [Agenzia Nazionale per la Protezione dell' Ambiente, Rome (Italy); Biancotto, R.; Bidoli, P.; Sepulcri, D. [Agenzia Regionale di Prevenzione e Protezione del Veneto, Venice (Italy). Dipt. provinciale di Venezia; Cavolo, F. [Smilax, Mira, VE (Italy)

2000-07-01

The phosphoric minerals utilized in phosphoric acid production, presents high concentrations of radioactive materials: U238, Th 232, K 40. The phosphogypsum is the waste material obtained in the phosphoric acid production in wet process. This type of production method is employed for many years in Venice lagoon (Porto Marghera chemical plants). In this paper are reported evaluations of radiological impact on aquatic environment of lagoon. [Italian] Con il termine di fosfogessi si intende comunemente il materiale di risulta che si ottiene nella produzione di acido fosforico attraverso la via umida (attacco acido). Questa tipologia di produzione che ha operato per diversi decenni a Porto Marghera, e' finalizzata allo scopo di ottenere acido fosforico principalmente per l'industria dei fertilizzanti e quindi come prodotto intermedio per la chimica e per le preparazioni alimentari. Il fosforo, elemento principale della reazione, era ricavato da rocce fosfatiche di origine sedimentaria marina provenienti per lo piu' dall'Africa settentrionale. Il sistema produttivo utilizzato negli impianti di Porto Marghera era basato su una reazione principale, che partendo dal minerale attraverso un attacco acido, produceva acido fosforico: Ca{sub 3}(PO{sub 4}){sub 2} (Minerale Fosforico) + 3H{sub 2}SO{sub 4} (Acido Solforico) + 3H{sub 2}O (Acqua) {yields} 2H{sub 3}PO{sub 4} (Acido fosforico) + 3CaSO{sub 4}H{sub 2}O (Solfato di calcio (gesso)). In particolare il minerale era preventivamente macinato e vagliato, quindi si procedeva alla sua miscelazione con l'acido fosforico ed alla successiva reazione del composto ottenuto.

Uranium extraction from phosphoric acid

International Nuclear Information System (INIS)

Araujo Figueiredo, C. de

1984-01-01

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

Solvent extraction of uranium, thorium, and rare earths with dialkyldithiophosphoric acids

International Nuclear Information System (INIS)

Haiduc, I.; Curtui, M.

1986-01-01

The separation conditions for throium (IV) in the presence of trivalent rare earths was investigated. The distribution ratios (D), extraction effectivity values (E%) and separation factor(S) were calculated for binary systems Th-La, Th-Ce, Th-Pr, Th-Sm. Di-(2-ethyl-hexyl)dithiophosphoric acid (HEhdtp) alone or mixtures of HEhdtp and trioctylphosphoshine oxide (TOPO) can be successfully used for separation of Thorium (IV) and rare earths

Method of separation of uranium from contaminating ions in an aqueous feed liquid containing uranyl ions

International Nuclear Information System (INIS)

Sundar, P.S.; Elikan, L.; Lyon, W.L.

1975-01-01

A coupled cationic/anionic method for the separation of uranium from contaminated aqueous solutions which contain uranyl ions is proposed. The fluid is extracted using an organic solvent containing a reagent which, together with the uranyl ions, forms a soluble aggregate in that solvent. As an example, 0.1 - 1 Mol/l Di-2-ethyl-hexyl-phosphorous acid in kerosene is mentioned. The organic solvent is then treated with a sealing liquid (volume ratio 20 - 35). For separation, an aqueous carbonate solution or a sulfuric acid solution can be used; the most favorable pH-values and concentrations for both cases are mentioned. The U +4 -ion at the sulfuric acid separation is subsequently oxidized to the uranyl ion with air. In each case, an extraction with an amine follows; after that, the amine is separated using an ammonium-carbonate solution and the uranium aggregate is precipitated, for example as ammonium uranyl tricarbonate, and then further processed to uranium oxide. The solvents and fluids used are led back in closed circuit; a flow diagram is given. (UWI) [de

Determination of mole fractions of ethyl-cellulose-containing monomers by NMR.

Science.gov (United States)

Kono, Hiroyuki

2017-06-05

Three samples of ethyl cellulose (EC) with different degrees of substitution (DS)-0.51, 1.41, and 2.28-were prepared by a slurry method using ethyl bromide as the etherification reagent. 1 H- 13 C HSQC and HSQC-TOCSY NMR spectral analysis allowed for complete assignment of the 1 H and 13 C chemical shifts, respectively, of eight anhydroglucose units (AGUs) comprising EC chains-un-, 2-mono-, 3-mono-, 6-mono-, 2,3-di-, 2,6-di-, 3,6-di-, and 2,3,6-tri-substituted AGUs. In addition, the lineshape of the quantitative 13 C NMR spectra of the three EC samples provided change in the mole fractions of these AGUs against DS, making it possible to estimate the reaction mechanism for the production of EC, elucidating reactivities of the hydroxyl groups at the 2, 3, and 6 positions of cellulose and interactions between the substituent groups within the same AGU and vicinal AGUs. Copyright © 2017 Elsevier Ltd. All rights reserved.

Hydrophobic Materials Based on Salts of Di(2-ethylhexyl)phosphoric Acid

Science.gov (United States)

Kizim, N. F.; Golubina, E. N.

2018-03-01

Interfacial formations of material based on metals di(2-ethylhexyl)phosphates of various metals exhibit hydrophobic properties. The contact angle of the surface, modified by the interfacial formations materials, could reach up to 140° depending on the nature of the solvent, the metal salt, the number of applications.

Membrane Separation of 2-Ethyl Hexyl Amine/1-Decene

KAUST Repository

Bawareth, Bander

2012-01-01

in this environment with reasonable and stable separation factor. This paper shows that Teflon AF 2400 and cellulose acetate produced interesting results in 1-decene/2-EHA separation. The separation factor of Teflon AF 2400 is 3 with a stable permeance of 1.1x10-2 L

Facilitated transport of Cr(III) through activated composite membrane containing di-(2-ethylhexyl)phosphoric acid (DEHPA) as carrier agent

Energy Technology Data Exchange (ETDEWEB)

Arslan, Gulsin [Department of Chemistry, Selcuk University, 42031, Campus, Konya (Turkey); Tor, Ali, E-mail: ator@selcuk.edu.tr [Department of Environmental Engineering, Selcuk University, 42031 Campus, Konya (Turkey); Cengeloglu, Yunus; Ersoz, Mustafa [Department of Chemistry, Selcuk University, 42031, Campus, Konya (Turkey)

2009-06-15

The facilitated transport of chromium(III) through activated composite membrane (ACM) containing di-(2-ethylhexyl) phosphoric acid (DEHPA) was investigated. DEHPA was immobilised by interfacial polymerisation on polysulfone layer which was deposited on non-woven fabric by using spin coater. Then, ACM was characterised by using scanning electron microscopy (SEM), contact angle measurements and atomic force microscopy (AFM). Initially, batch experiments of liquid-liquid distribution of Cr(III) and the extractant (DEHPA) were carried out to determine the appropriate pH of the feed phase and the results showed that maximum extraction of Cr(III) was achieved at a pH of 4. It was also found that Cr(III) and DEHPA reacted in 1/1 molar ratio. The effects of Cr(III) (in feed phase), HCl (in stripping phase) and DEHPA (in ACM) concentrations were investigated. DEHPA concentration varies from 0.1 to 1.0 M and it was determined that the transport of Cr(III) increased with the carrier concentration up to 0.8 M. It was also observed that the transport of Cr(III) through the ACM tended to increase with Cr(III) and HCl concentrations. The stability of ACM was also confirmed with replicate experiments.

Facilitated transport of Cr(III) through activated composite membrane containing di-(2-ethylhexyl)phosphoric acid (DEHPA) as carrier agent

International Nuclear Information System (INIS)

Arslan, Gulsin; Tor, Ali; Cengeloglu, Yunus; Ersoz, Mustafa

2009-01-01

The facilitated transport of chromium(III) through activated composite membrane (ACM) containing di-(2-ethylhexyl) phosphoric acid (DEHPA) was investigated. DEHPA was immobilised by interfacial polymerisation on polysulfone layer which was deposited on non-woven fabric by using spin coater. Then, ACM was characterised by using scanning electron microscopy (SEM), contact angle measurements and atomic force microscopy (AFM). Initially, batch experiments of liquid-liquid distribution of Cr(III) and the extractant (DEHPA) were carried out to determine the appropriate pH of the feed phase and the results showed that maximum extraction of Cr(III) was achieved at a pH of 4. It was also found that Cr(III) and DEHPA reacted in 1/1 molar ratio. The effects of Cr(III) (in feed phase), HCl (in stripping phase) and DEHPA (in ACM) concentrations were investigated. DEHPA concentration varies from 0.1 to 1.0 M and it was determined that the transport of Cr(III) increased with the carrier concentration up to 0.8 M. It was also observed that the transport of Cr(III) through the ACM tended to increase with Cr(III) and HCl concentrations. The stability of ACM was also confirmed with replicate experiments.

TRANSPORT PROPERTIES FOR 1-ETHYL-3-METHYLIMIDAZOLIUM n-ALKYL SULFATES: POSSIBLE EVIDENCE OF GROTTHUSS MECHANISM

International Nuclear Information System (INIS)

García-Garabal, S.; Vila, J.; Rilo, E.; Domínguez-Pérez, M.; Segade, L.; Tojo, E.; Verdía, P.; Varela, L.M.; Cabeza, O.

2017-01-01

The objective of this work was to study the effect of the temperature and the lengthening of the linear alkyl chain of the anion in the transport physical properties of the pure ionic liquids 1-ethyl-3-methyl imidazolium n-alkyl sulphate (being n = 0, 1, 2, 4, 6 and 8). Density, viscosity and electrical conductivities were measured at atmospheric pressure in a wide temperature range. In the bibliography, data existed for these magnitudes for all ionic liquids studied but none of these had information about the electrical conductivity of 1-ethyl-3-methyl imidazolium n-alkyl sulfate whith n = 0, 4, 6 and 8. The experimental results show clearly 1-ethyl-3-methyl imidazolium hydrogen sulphate cannot be considered part of the 1-ethyl-3-methyl imidazolium n-alkyl sulphate family because of its hydrogen bonding ability. Results of density and viscosity behave as expected. However, in the case of the electrical conductivity due to the lack of alkyl chain in the hydrogen sulfate we expected to get extreme values but in practise, we obtained intermediate values between 1-ethyl-3-methyl imidazolium butyl sulphate and 1-ethyl-3-methyl imidazolium hexyl sulphate. This suggests that a Grotthus mechanism exists as result of a protonic current in addition to ionic conductivity, being Waldeńs plot consistent with this idea.

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

International Nuclear Information System (INIS)

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

1987-01-01

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

Synthesis and crystal structures of multifunctional tosylates as basis for star-shaped poly(2-ethyl-2-oxazolines

Directory of Open Access Journals (Sweden)

Richard Hoogenboom

2010-09-01

Full Text Available The synthesis of well-defined polymer architectures is of major importance for the development of complex functional materials. In this contribution, we discuss the synthesis of a range of multifunctional star-shaped tosylates as potential initiators for the living cationic ring-opening polymerization (CROP of 2-oxazolines resulting in star-shaped polymers. The synthesis of the tosylates was performed by esterification of the corresponding alcohols with tosyl chloride. Recrystallization of these tosylate compounds afforded single crystals, and the X-ray crystal structures of di-, tetra- and hexa-tosylates are reported. The use of tetra- and hexa-tosylates, based on (dipentaerythritol as initiators for the CROP of 2-ethyl-2-oxazoline, resulted in very slow initiation and ill-defined polymers, which is most likely caused by steric hindrance in these initiators. As a consequence, a porphyrin-cored tetra-tosylate initiator was prepared, which yielded a well-defined star-shaped poly(2-ethyl-2-oxazoline by CROP as demonstrated by SEC with RI, UV and diode-array detectors, as well as by 1H NMR spectroscopy.

Method for recovery of uranium from phosphoric acid

International Nuclear Information System (INIS)

Duarte Neto, J.

1984-01-01

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

Luminescent properties of phosphor converted LED using an orange-emitting Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} phosphor

Energy Technology Data Exchange (ETDEWEB)

Song, Hee Jo; Yim, Dong Kyun [Department of Materials Science and Engineering, College of Engineering, Seoul National University, Daehak-dong, Gwanak-gu, Seoul 151-744 (Korea, Republic of); Cho, In-Sun [Department of Mechanical Engineering, Stanford University, CA 94305 (United States); Roh, Hee-Suk; Kim, Ju Seong [Department of Materials Science and Engineering, College of Engineering, Seoul National University, Daehak-dong, Gwanak-gu, Seoul 151-744 (Korea, Republic of); Kim, Dong-Wan, E-mail: dwkim@ajou.ac.kr [Department of Materials Science and Engineering, Ajou University, Woncheon-dong, San 5, Yeongtong-gu, Suwon 443-749 (Korea, Republic of); Hong, Kug Sun, E-mail: kshongss@plaza.snu.ac.kr [Department of Materials Science and Engineering, College of Engineering, Seoul National University, Daehak-dong, Gwanak-gu, Seoul 151-744 (Korea, Republic of)

2012-12-15

Graphical abstract: Display Omitted Highlights: ► Phase-pure Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} powders were synthesized by a solid state reaction process. ► The optimum emission intensity was observed at the Eu{sup 2+} ion concentration of 0.006. ► The dipole–dipole interaction was the major concentration quenching mechanism. ► The pc-LED coated with Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} had higher CRI than commercial red phosphor. -- Abstract: A series of orange-emitting Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} phosphors were synthesized by a conventional solid-state reaction method. The as-prepared phosphors were characterized by X-ray powder diffraction (XRD), fluorescence spectroscopy, and spectroradiometry. XRD showed that all prepared samples exhibited a monoclinic Rb{sub 2}CaP{sub 2}O{sub 7} phase. Fluorescence spectroscopy showed that the photoluminescence efficiency of Rb{sub 2}Ca{sub 1−x}P{sub 2}O{sub 7}:Eu{sub x}{sup 2+} phosphors increased with increasing Eu{sup 2+} concentration until x = 0.006, then decreased at higher concentrations, due to a concentration quenching effect. The thermal activation energy was also measured to be 0.40 eV. Furthermore, a phosphor-converted LED (pc-LED) coated with Rb{sub 2}Ca{sub 0.994}P{sub 2}O{sub 7}:Eu{sub 0.006}{sup 2+} was fabricated, which exhibited bright orange emission under a forward bias, from 200 to 300 mA. The color rendering index (CRI) of pc-LED coated with Rb{sub 2}Ca{sub 0.994}P{sub 2}O{sub 7}:Eu{sub 0.006}{sup 2+} was higher than the CRI of pc-LED coated with commercial red phosphor, due to the broad emission band of Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} phosphor. In applying with three-band pc-LEDs, moreover, white pc-LED using Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} phosphor had a higher CRI, than using commercial phosphor. These results indicated that Rb{sub 2}CaP{sub 2}O{sub 7}:Eu{sup 2+} phosphor could be a good candidate for a near-UV based w-LED.

Extraction of plutonium from phosphate containing nitric acid solutions using DHDECMP as extractant (Preprint no. SSC-03)

International Nuclear Information System (INIS)

Sagar, V.B.; Pawar, S.M.; Joshi, A.R.; Kasar, U.M.; Sivaramkrishnan, C.K.

1991-01-01

Distribution data for the extraction of Pu(IV) by DHDECMP (Di-hexyl, N-N-diethylcarbamoylmethylphosphonate) in xylene from aqueous nitric acid and its mixtures with sulphuric acid and phosphoric acid were obtained to explore the feasibility of recovery of Pu(IV) from analytical waste generated in the laboratory. Based on the data obtained, conditions for recovery of plutonium are suggested. (author). 3 refs., 3 tabs

New triarylamine organic dyes containing the 9-hexyl-2-(hexyloxy)-9H-carbazole for dye-sensitized solar cells

International Nuclear Information System (INIS)

Su, Jianyang; Chen, Yu; Wu, Yungen; Ghimire, Raju Prasad; Xu, Yingjun; Liu, Xiujie; Wang, Zhihui; Liang, Mao

2017-01-01

Highlights: •9-hexyl-2-(hexyloxy)-9H-carbazole (HHCBZ) was synthesized for organic dyes. •Three new triarylamine sensitizers based on the HHCBZ unit were synthesized. •The HHCBZ unit outperforms the HCBZ when used as an electron donor. •An efficiency of 8.67% was achieved by M92 with the HHCBZ donor. -- Abstract: Developing carbazole derivatives as the electron donor for organic dyes have attracted extensive interest recently. Three organic dyes M92-94 based on the 9-hexyl-2-(hexyloxy)-9H-carbazole (HHCBZ) electron donor have been successfully designed and synthesized for dye-sensitized solar cells. M95 with the 9-hexyl-9H-carbazole (HCBZ) unit has also been synthesized for comparison. An introduction of the HHCBZ unit in triarylamine brings several advantages: (i) red shifting the absorption peak and increasing the maximum molar absorption coefficient of absorption bands; (ii) decreasing the charge recombination in cobalt cells as well as iodine cells; (iii) enhancing photocurrent/photovoltage and thus the power conversion efficiencies of cobalt cells as well as iodine cells. Devices prepared with M92 show consistently higher light-to-electric energy conversion efficiencies, with the champion device reaching 8.67%, surpassing M93-95.

Biochemistry Oxidation Process for Treatment the Simulation of Organic Liquid Radioactive Waste

International Nuclear Information System (INIS)

Gunandjar; Zainus Salimin; Sugeng Purnomo; Ratiko

2010-01-01

The nuclear industry activities generate the organic liquid wastes such as detergent waste from laundry, solvent waste of 30% TBP (tri-n-butyl phosphate) in kerosene from purification or recovery of uranium from rejection of nuclear fuel element fabrication, and solvent waste containing D 2 EHPA (di-2-ethyl hexyl phosphoric acid) and TOPO (trioctyl phospine oxide) in kerosene from phosphoric acid purification. The wastes are included in category of the hazard and poison materials which also radioactive, so that the wastes have to be treated to detoxification of the hazard and poison materials and decontamination of the radionuclides. The research of biochemistry oxidation process for treatment the simulation of organic liquid radioactive waste from laundry using mixture of aerobe bacteria of bacillus sp, pseudomonas sp, arthrobacter sp, and aeromonas sp have been carried out. The waste containing detergent 1,496 g/Litre, activity 10 -1 Ci/m 3 , with COD (Chemical Oxygen Demand) 128, BOD (Biological Oxygen Demand) 68 and TSS (Total Suspended Solid) 1000 ppm, it is treated by biochemistry oxidation with addition of bacteria which be fed nutrition of nitrogen and phosphor, and aeration. The result show that the bacteria can decompose the detergent to become carbon dioxyde and water so that can fulfill the quality standard of water group-B with content of BOD and COD are 6 and 10 ppm respectively, the time of decomposition is needed 106 hours to be fulfill the quality standard of water. The longer of process time will give bigger the total solid content in sludge, because the biomass generated from the colony of bacteria which life and dead to so much. (author)

Technology of uranium recovery from wet-process phosphoric acid

Energy Technology Data Exchange (ETDEWEB)

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

1982-12-01

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

Urinary di-(2-ethylhexyl) phthalate metabolites for detecting transfusion of autologous blood stored in plasticizer-free bags.

Science.gov (United States)

Leuenberger, Nicolas; Barras, Laura; Nicoli, Raul; Robinson, Neil; Baume, Norbert; Lion, Niels; Barelli, Stefano; Tissot, Jean-Daniel; Saugy, Martial

2016-03-01

Autologous blood transfusion (ABT) efficiently increases sport performance and is the most challenging doping method to detect. Current methods for detecting this practice center on the plasticizer di(2-ethlyhexyl) phthalate (DEHP), which enters the stored blood from blood bags. Quantification of this plasticizer and its metabolites in urine can detect the transfusion of autologous blood stored in these bags. However, DEHP-free blood bags are available on the market, including n-butyryl-tri-(n-hexyl)-citrate (BTHC) blood bags. Athletes may shift to using such bags to avoid the detection of urinary DEHP metabolites. A clinical randomized double-blinded two-phase study was conducted of healthy male volunteers who underwent ABT using DEHP-containing or BTHC blood bags. All subjects received a saline injection for the control phase and a blood donation followed by ABT 36 days later. Kinetic excretion of five urinary DEHP metabolites was quantified with liquid chromatography coupled with tandem mass spectrometry. Surprisingly, considerable levels of urinary DEHP metabolites were observed up to 1 day after blood transfusion with BTHC blood bags. The long-term metabolites mono-(2-ethyl-5-carboxypentyl) phthalate and mono-(2-carboxymethylhexyl) phthalate were the most sensitive biomarkers to detect ABT with BTHC blood bags. Levels of DEHP were high in BTHC bags (6.6%), the tubing in the transfusion kit (25.2%), and the white blood cell filter (22.3%). The BTHC bag contained DEHP, despite being labeled DEHP-free. Urinary DEHP metabolite measurement is a cost-effective way to detect ABT in the antidoping field even when BTHC bags are used for blood storage. © 2015 AABB.

Photocatalytic effects for the TiO2-coated phosphor materials

International Nuclear Information System (INIS)

Yoon, Jin-Ho; Jung, Sang-Chul; Kim, Jung-Sik

2011-01-01

Research highlights: → The photocatalytic behavior of the coupling of TiO 2 with phosphorescent materials. → The photobleaching of an MB aqueous solution under visible light irradiation. → The ALD TiO 2 -coated phosphor composite showed much higher photocatalytic reactivity. → The light emitted from the phosphors contributed to the photo-generation. - Abstract: This study investigated the photocatalytic behavior of the coupling of TiO 2 with phosphorescent materials. A TiO 2 thin film was deposited on CaAl 2 O 4 :Eu 2+ ,Nd 3+ phosphor particles by using atomic layer deposition (ALD), and its photocatalytic reaction was investigated by the photobleaching of an aqueous solution of methylene-blue (MB) under visible light irradiation. To clarify the mechanism of the TiO 2 -phosphorescent materials, two different samples of TiO 2 -coated phosphor and TiO 2 -Al 2 O 3 -coated phosphor particles were prepared. The photocatalytic mechanisms of the ALD TiO 2 -coated phosphor powders were different from those of the pure TiO 2 and TiO 2 -Al 2 O 3 -coated phosphor. The absorbance in a solution of the ALD TiO 2 -coated phosphor decreased much faster than that of pure TiO 2 under visible irradiation. In addition, the ALD TiO 2 -coated phosphor showed moderately higher photocatalytic degradation of MB solution than the TiO 2 -Al 2 O 3 -coated phosphor did. The TiO 2 -coated phosphorescent materials were characterized by transmission electron microscopy (TEM), Auger electron spectroscopy (AES) and X-ray photon spectroscopy (XPS).

Photocatalytic degradation of paraoxon-ethyl in aqueous solution using titania nanoparticulate film

International Nuclear Information System (INIS)

Prasad, G.K.; Ramacharyulu, P.V.R.K.; Kumar, J. Praveen; Srivastava, A.R.; Singh, Beer

2012-01-01

Photocatalytic degradation of paraoxon-ethyl (o,o-diethyl o-(4-nitrophenyl) phosphate), a well known surrogate of chemical warfare agents, in aqueous solution was studied by using titania nanoparticulate film. Reaction followed pseudo first order behaviour. Photolytic degradation reaction of paraoxon-ethyl demonstrated relatively low rate with a value of rate constant of 2.5 × 10 −3 min −1 . Whereas, degradation reaction in the presence of titania nanoparticulate film and UV light displayed enhanced rate with a value of rate constant of 6.9 × 10 −3 min −1 due to photocatalysis. Gas chromatography–mass spectrometry analysis showed the formation of p-nitrophenol, o,o-diethyl phosphonic acid, o-ethyl, diphosphonic acid, phosphoric acid, dimerized product of o,o-diethyl phosphonic acid, acetaldehyde, and carbon dioxide due to photocatalytic degradation of paraoxon-ethyl. It indicates that, photocatalytic degradation reaction begins with destruction of P–O–C bonds. Subsequently, P, C atoms were found to be oxidized gradually, and contributed to its photocatalytic degradation. - Highlights: ► Synthesis of titania nanoparticles by sol–gel method. ► Fabrication of titania nanoparticulate film by dip coating. ► Paraoxon ethyl degradation reactions followed pseudo first order behaviour. ► Paraoxon-ethyl degraded to non toxic compounds like CO 2 , acetaldehyde, and nitrophenol.

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

International Nuclear Information System (INIS)

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

1994-01-01

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

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

Insight into the adsorption mechanisms of trace organic carbon on biological treatment process.

Science.gov (United States)

Zolfaghari, Mehdi; Drogui, Patrick; Brar, Satinder Kaur; Buelna, Gerardo; Dubé, Rino

2017-09-01

The presence of recalcitrant dissolved organic matter (DOM) could have a significant effect on the adsorption mechanism and capacity of the sludge for many trace organic carbons (TrOCs). In this study, adsorption of three TrOCs on the sludge and HA was investigated. The results revealed that neutral hydrophilic compounds had an insignificant interaction with both sludge and HA. Positively charged compounds, such as fluoranthene, had more affinity toward HA than sludge with solid/liquid partitioning of 57 and 3.2 L/g, respectively. The adsorption intensity (K f ) of di-2-ethyl hexyl phthalate was 0.5 and 1.13 for the HA and the sludge, respectively. By introducing the sludge to the solution of HA and TrOCs that already reached equilibrium, the sludge adsorption capacity in the presence of HA was investigated. The finding showed that at the lower concentration, adsorption of HA on the sludge was considered as the main removal pathway for the adsorbed emerging contaminants, as 70 mg of HA was adsorbed by a gram of sludge. For the higher concentration, desorption of TrOCs from DOM into the sludge comprised 15-30% of total removal efficiency. CBZ: carbamazepine; DEHP: di-2-ethyl hexyl phthalate; DOM: dissolved organic matter; FLAN: fluoranthene; f oc : fraction of organic carbon; HA: humic acid; Log Kow: octanol-water partition coefficient; PAH: polycyclic aromatic hydrocarbon TS: total solid; TrOCs: trace organic carbons VS: volatile solid.

Counter current extraction of phosphoric acid: Food grade acid production

International Nuclear Information System (INIS)

Shlewit, H.; AlIbrahim, M.

2009-01-01

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

Effects of the UV-filter 2-ethyl-hexyl-4-trimethoxycinnamate (EHMC) on expression of genes involved in hormonal pathways in fathead minnows (Pimephales promelas) and link to vitellogenin induction and histology

International Nuclear Information System (INIS)

Christen, Verena; Zucchi, Sara; Fent, Karl

2011-01-01

UV-filters are increasingly used in cosmetics and in the protection of materials against UV-irradiation, and ultimately they reach aquatic systems. The lipophilic UV-filter 2-ethyl-hexyl-4-trimethoxycinnamate (EHMC) belongs to one of the most frequently used UV-filters and accumulates in aquatic animals. Despite its ubiquitous presence in water and biota, very little is known about its potential hormonal effects on aquatic organisms. In our study, we evaluated the effects of measured water concentration of 5.4, 37.5, 244.5 and 394 μg/L EHMC on the expression of genes involved in hormonal pathways in the liver, testis and brain of male and female fathead minnows (Pimephales promelas). We compare the transcription profile with the plasma vitellogenin (VTG) content, secondary sex characteristics, and gonad histology. Transcripts of the androgen receptor (ar) were significantly down-regulated in the liver of females at 37.5, 244.5 μg/L and 394 μg/L EHMC. Additionally, the 3β-hydroxysteroid dehydrogenase (3β-HSD) transcript was significantly decreased in the liver of males at 37.5, 244.5 and 394 μg/L EHMC, and at 244.5 and 394 μg/L EHMC in females. The expressional changes were tissue-specific in most cases, being most significant in the liver. Vitellogenin plasma concentration was significantly increased at 244.5 μg/L EHMC in males. EHMC induced significant histological changes in testes and ovaries at 394 μg/L. Testes displayed a decrease in spermatocytes, and ovaries a decrease in previtellogenic oocytes. The induction of VTG plasma concentration and the histological changes in gonads suggest an estrogenic and/or antiandrogenic activity of EHMC. On the other hand, the gene expression profile shows an antiestrogenic (e.g.: down-regulation of esr1) activity of EHMC. In conclusion, our data demonstrate that EHMC displays low but multiple hormonal activities in fish.

Effects of the UV-filter 2-ethyl-hexyl-4-trimethoxycinnamate (EHMC) on expression of genes involved in hormonal pathways in fathead minnows (Pimephales promelas) and link to vitellogenin induction and histology

Energy Technology Data Exchange (ETDEWEB)

Christen, Verena; Zucchi, Sara [University of Applied Sciences Northwestern Switzerland, School of Life Sciences, Gruendenstrasse 40, CH-4132 Muttenz (Switzerland); Fent, Karl, E-mail: karl.fent@fhnw.ch [University of Applied Sciences Northwestern Switzerland, School of Life Sciences, Gruendenstrasse 40, CH-4132 Muttenz (Switzerland); Swiss Federal Institute of Technology Zuerich (ETH Zuerich), Department of Environmental Sciences, 8092 Zuerich (Switzerland)

2011-04-15

UV-filters are increasingly used in cosmetics and in the protection of materials against UV-irradiation, and ultimately they reach aquatic systems. The lipophilic UV-filter 2-ethyl-hexyl-4-trimethoxycinnamate (EHMC) belongs to one of the most frequently used UV-filters and accumulates in aquatic animals. Despite its ubiquitous presence in water and biota, very little is known about its potential hormonal effects on aquatic organisms. In our study, we evaluated the effects of measured water concentration of 5.4, 37.5, 244.5 and 394 {mu}g/L EHMC on the expression of genes involved in hormonal pathways in the liver, testis and brain of male and female fathead minnows (Pimephales promelas). We compare the transcription profile with the plasma vitellogenin (VTG) content, secondary sex characteristics, and gonad histology. Transcripts of the androgen receptor (ar) were significantly down-regulated in the liver of females at 37.5, 244.5 {mu}g/L and 394 {mu}g/L EHMC. Additionally, the 3{beta}-hydroxysteroid dehydrogenase (3{beta}-HSD) transcript was significantly decreased in the liver of males at 37.5, 244.5 and 394 {mu}g/L EHMC, and at 244.5 and 394 {mu}g/L EHMC in females. The expressional changes were tissue-specific in most cases, being most significant in the liver. Vitellogenin plasma concentration was significantly increased at 244.5 {mu}g/L EHMC in males. EHMC induced significant histological changes in testes and ovaries at 394 {mu}g/L. Testes displayed a decrease in spermatocytes, and ovaries a decrease in previtellogenic oocytes. The induction of VTG plasma concentration and the histological changes in gonads suggest an estrogenic and/or antiandrogenic activity of EHMC. On the other hand, the gene expression profile shows an antiestrogenic (e.g.: down-regulation of esr1) activity of EHMC. In conclusion, our data demonstrate that EHMC displays low but multiple hormonal activities in fish.

Effects of the UV-filter 2-ethyl-hexyl-4-trimethoxycinnamate (EHMC) on expression of genes involved in hormonal pathways in fathead minnows (Pimephales promelas) and link to vitellogenin induction and histology.

Science.gov (United States)

Christen, Verena; Zucchi, Sara; Fent, Karl

2011-04-01

UV-filters are increasingly used in cosmetics and in the protection of materials against UV-irradiation, and ultimately they reach aquatic systems. The lipophilic UV-filter 2-ethyl-hexyl-4-trimethoxycinnamate (EHMC) belongs to one of the most frequently used UV-filters and accumulates in aquatic animals. Despite its ubiquitous presence in water and biota, very little is known about its potential hormonal effects on aquatic organisms. In our study, we evaluated the effects of measured water concentration of 5.4, 37.5, 244.5 and 394 μg/L EHMC on the expression of genes involved in hormonal pathways in the liver, testis and brain of male and female fathead minnows (Pimephales promelas). We compare the transcription profile with the plasma vitellogenin (VTG) content, secondary sex characteristics, and gonad histology. Transcripts of the androgen receptor (ar) were significantly down-regulated in the liver of females at 37.5, 244.5 μg/L and 394 μg/L EHMC. Additionally, the 3β-hydroxysteroid dehydrogenase (3β-HSD) transcript was significantly decreased in the liver of males at 37.5, 244.5 and 394 μg/L EHMC, and at 244.5 and 394 μg/L EHMC in females. The expressional changes were tissue-specific in most cases, being most significant in the liver. Vitellogenin plasma concentration was significantly increased at 244.5 μg/L EHMC in males. EHMC induced significant histological changes in testes and ovaries at 394 μg/L. Testes displayed a decrease in spermatocytes, and ovaries a decrease in previtellogenic oocytes. The induction of VTG plasma concentration and the histological changes in gonads suggest an estrogenic and/or antiandrogenic activity of EHMC. On the other hand, the gene expression profile shows an antiestrogenic (e.g.: down-regulation of esr1) activity of EHMC. In conclusion, our data demonstrate that EHMC displays low but multiple hormonal activities in fish. Copyright © 2011 Elsevier B.V. All rights reserved.

Photocatalytic degradation of paraoxon-ethyl in aqueous solution using titania nanoparticulate film

Energy Technology Data Exchange (ETDEWEB)

Prasad, G.K., E-mail: gkprasad2001@yahoo.com; Ramacharyulu, P.V.R.K.; Kumar, J. Praveen; Srivastava, A.R.; Singh, Beer

2012-06-30

Photocatalytic degradation of paraoxon-ethyl (o,o-diethyl o-(4-nitrophenyl) phosphate), a well known surrogate of chemical warfare agents, in aqueous solution was studied by using titania nanoparticulate film. Reaction followed pseudo first order behaviour. Photolytic degradation reaction of paraoxon-ethyl demonstrated relatively low rate with a value of rate constant of 2.5 Multiplication-Sign 10{sup -3} min{sup -1}. Whereas, degradation reaction in the presence of titania nanoparticulate film and UV light displayed enhanced rate with a value of rate constant of 6.9 Multiplication-Sign 10{sup -3} min{sup -1} due to photocatalysis. Gas chromatography-mass spectrometry analysis showed the formation of p-nitrophenol, o,o-diethyl phosphonic acid, o-ethyl, diphosphonic acid, phosphoric acid, dimerized product of o,o-diethyl phosphonic acid, acetaldehyde, and carbon dioxide due to photocatalytic degradation of paraoxon-ethyl. It indicates that, photocatalytic degradation reaction begins with destruction of P-O-C bonds. Subsequently, P, C atoms were found to be oxidized gradually, and contributed to its photocatalytic degradation. - Highlights: Black-Right-Pointing-Pointer Synthesis of titania nanoparticles by sol-gel method. Black-Right-Pointing-Pointer Fabrication of titania nanoparticulate film by dip coating. Black-Right-Pointing-Pointer Paraoxon ethyl degradation reactions followed pseudo first order behaviour. Black-Right-Pointing-Pointer Paraoxon-ethyl degraded to non toxic compounds like CO{sub 2}, acetaldehyde, and nitrophenol.

Synergistic extraction of Am(III) using HTTA and bi-functional (DHDECMP) and mono-functional (TBP) donors

International Nuclear Information System (INIS)

Pai, S.A.; Lohithakshan, K.V.; Mithapara, P.D.; Aggarwal, S.K.

1999-01-01

The equilibrium constant (log Ks) for the organic phase synergistic reaction for Am(III)-HTTA system with bi-functional neutral donor di-hexyl di-ethyl carbamoylmethyl phosphonate (DHDECMP) was found to be about two orders of magnitude higher than that of the mono-functional neutral donor (TBP) with comparable basicity values. This log Ks value along with a large positive entropy change with DHDECMP compared to that with TBP confirms that the neutral donors like DHDECMP behave as bi-functional, in sharp contrast to its mono-functional behaviour in Pu(VI). (author)

Degradation of di(2-ethyl hexyl) phthalate by Fusarium culmorum: Kinetics, enzymatic activities and biodegradation pathway based on quantum chemical modelingpathway based on quantum chemical modeling

International Nuclear Information System (INIS)

Ahuactzin-Pérez, Miriam; Tlecuitl-Beristain, Saúl; García-Dávila, Jorge; González-Pérez, Manuel; Gutiérrez-Ruíz, María Concepción; Sánchez, Carmen

2016-01-01

Di(2-ethylhexyl) phthalate (DEHP) is a plasticizer widely used in the manufacture of plastics, and it is an environmental contaminant. The specific growth rate (μ), maximum biomass (X_m_a_x), biodegradation constant of DEHP (k), half-life (t_1_/_2) of DEHP biodegradation and removal efficiency of DEHP, esterase and laccase specific activities, and enzymatic yield parameters were evaluated for Fusarium culmorum grown on media containing glucose and different concentrations of DEHP (0, 500 and 1000 mg/L). The greatest μ and the largest X_m_a_x occurred in media supplemented with 1000 mg of DEHP/L. F. culmorum degraded 95% of the highest amount of DEHP tested (1000 mg/L) within 60 h of growth. The k and t_1_/_2 were 0.024 h"−"1 and 28 h, respectively, for both DEHP concentrations. The removal efficiency of DEHP was 99.8% and 99.9% for 1000 and 500 mg/L, respectively. Much higher specific esterase activity than specific laccase activity was observed in all media tested. The compounds of biodegradation of DEHP were identified by GC–MS. A DEHP biodegradation pathway by F. culmorum was proposed on the basis of the intermolecular flow of electrons of the identified intermediate compounds using quantum chemical modeling. DEHP was fully metabolized by F. culmorum with butanediol as the final product. This fungus offers great potential in bioremediation of environments polluted with DEHP. - Highlights: • F. culmorum degraded 95% of DEHP (1000 mg/L) within 60 h. • Removal efficiency of DEHP was 99.8% and 99.9% for 1000 and 500 mg/L, respectively. • DEHP was fully metabolized by F. culmorum, with butanediol as the final product. • A DEHP biodegradation pathway was proposed using on quantum chemical modeling.

Degradation of di(2-ethyl hexyl) phthalate by Fusarium culmorum: Kinetics, enzymatic activities and biodegradation pathway based on quantum chemical modelingpathway based on quantum chemical modeling

Energy Technology Data Exchange (ETDEWEB)

Ahuactzin-Pérez, Miriam [Doctorado en Biología Experimental, Universidad Autónoma Metropolitana-Iztapalapa (UAM-I) (Mexico); Facultad de Agrobiología, Universidad Autónoma de Tlaxcala, Ixtacuixtla, Tlaxcala (Mexico); Tlecuitl-Beristain, Saúl; García-Dávila, Jorge [Universidad Politécnica de Tlaxcala, San Pedro Xalcatzinco, Tepeyanco, Tlaxcala CP 90180 (Mexico); González-Pérez, Manuel [Universidad Popular Autónoma del Estado de Puebla, Puebla CP 72410 (Mexico); Gutiérrez-Ruíz, María Concepción [Departamento de Ciencias de la Salud, Universidad Autónoma Metropolitana-Iztapalapa, D.F (Mexico); Sánchez, Carmen, E-mail: sanher6@hotmail.com [Laboratory of Biotechnology, Research Centre for Biological Sciences, Universidad Autónoma de Tlaxcala, Ixtacuixtla, Tlaxcala CP. 90062 (Mexico)

2016-10-01

Di(2-ethylhexyl) phthalate (DEHP) is a plasticizer widely used in the manufacture of plastics, and it is an environmental contaminant. The specific growth rate (μ), maximum biomass (X{sub max}), biodegradation constant of DEHP (k), half-life (t{sub 1/2}) of DEHP biodegradation and removal efficiency of DEHP, esterase and laccase specific activities, and enzymatic yield parameters were evaluated for Fusarium culmorum grown on media containing glucose and different concentrations of DEHP (0, 500 and 1000 mg/L). The greatest μ and the largest X{sub max} occurred in media supplemented with 1000 mg of DEHP/L. F. culmorum degraded 95% of the highest amount of DEHP tested (1000 mg/L) within 60 h of growth. The k and t{sub 1/2} were 0.024 h{sup −1} and 28 h, respectively, for both DEHP concentrations. The removal efficiency of DEHP was 99.8% and 99.9% for 1000 and 500 mg/L, respectively. Much higher specific esterase activity than specific laccase activity was observed in all media tested. The compounds of biodegradation of DEHP were identified by GC–MS. A DEHP biodegradation pathway by F. culmorum was proposed on the basis of the intermolecular flow of electrons of the identified intermediate compounds using quantum chemical modeling. DEHP was fully metabolized by F. culmorum with butanediol as the final product. This fungus offers great potential in bioremediation of environments polluted with DEHP. - Highlights: • F. culmorum degraded 95% of DEHP (1000 mg/L) within 60 h. • Removal efficiency of DEHP was 99.8% and 99.9% for 1000 and 500 mg/L, respectively. • DEHP was fully metabolized by F. culmorum, with butanediol as the final product. • A DEHP biodegradation pathway was proposed using on quantum chemical modeling.

Synthesis and Thermal Properties of Acrylonitrile/Butyl Acrylate/Fumaronitrile and Acrylonitrile/Ethyl Hexyl Acrylate/Fumaronitrile Terpolymers as a Potential Precursor for Carbon Fiber

Directory of Open Access Journals (Sweden)

Siti Nurul Ain Md Jamil

2014-09-01

Full Text Available A synthesis of acrylonitrile (AN/butyl acrylate (BA/fumaronitrile (FN and AN/EHA (ethyl hexyl acrylate/FN terpolymers was carried out by redox polymerization using sodium bisulfite (SBS and potassium persulphate (KPS as initiator at 40 °C. The effect of comonomers, BA and EHA and termonomer, FN on the glass transition temperature (Tg and stabilization temperature was studied using Differential Scanning Calorimetry (DSC. The degradation behavior and char yield were obtained by Thermogravimetric Analysis. The conversions of AN, comonomers (BA and EHA and FN were 55%–71%, 85%–91% and 76%–79%, respectively. It was found that with the same comonomer feed (10%, the Tg of AN/EHA copolymer was lower at 63 °C compared to AN/BA copolymer (70 °C. AN/EHA/FN terpolymer also exhibited a lower Tg at 63 °C when compared to that of the AN/BA/FN terpolymer (67 °C. By incorporating BA and EHA into a PAN system, the char yield was reduced to ~38.0% compared to that of AN (~47.7%. It was found that FN reduced the initial cyclization temperature of AN/BA/FN and AN/EHA/FN terpolymers to 228 and 221 °C, respectively, in comparison to that of AN/BA and AN/EHA copolymers (~260 °C. In addition, FN reduced the heat liberation per unit time during the stabilization process that consequently reduced the emission of volatile group during this process. As a result, the char yields of AN/BA/FN and AN/EHA/FN terpolymers are higher at ~45.1% and ~43.9%, respectively, as compared to those of AN/BA copolymer (37.1% and AN/EHA copolymer (38.0%.

Synthesis and Thermal Properties of Acrylonitrile/Butyl Acrylate/Fumaronitrile and Acrylonitrile/Ethyl Hexyl Acrylate/Fumaronitrile Terpolymers as a Potential Precursor for Carbon Fiber.

Science.gov (United States)

Jamil, Siti Nurul Ain Md; Daik, Rusli; Ahmad, Ishak

2014-09-01

A synthesis of acrylonitrile (AN)/butyl acrylate (BA)/fumaronitrile (FN) and AN/EHA (ethyl hexyl acrylate)/FN terpolymers was carried out by redox polymerization using sodium bisulfite (SBS) and potassium persulphate (KPS) as initiator at 40 °C. The effect of comonomers, BA and EHA and termonomer, FN on the glass transition temperature (T g ) and stabilization temperature was studied using Differential Scanning Calorimetry (DSC). The degradation behavior and char yield were obtained by Thermogravimetric Analysis. The conversions of AN, comonomers (BA and EHA) and FN were 55%-71%, 85%-91% and 76%-79%, respectively. It was found that with the same comonomer feed (10%), the T g of AN/EHA copolymer was lower at 63 °C compared to AN/BA copolymer (70 °C). AN/EHA/FN terpolymer also exhibited a lower T g at 63 °C when compared to that of the AN/BA/FN terpolymer (67 °C). By incorporating BA and EHA into a PAN system, the char yield was reduced to ~38.0% compared to that of AN (~47.7%). It was found that FN reduced the initial cyclization temperature of AN/BA/FN and AN/EHA/FN terpolymers to 228 and 221 °C, respectively, in comparison to that of AN/BA and AN/EHA copolymers (~260 °C). In addition, FN reduced the heat liberation per unit time during the stabilization process that consequently reduced the emission of volatile group during this process. As a result, the char yields of AN/BA/FN and AN/EHA/FN terpolymers are higher at ~45.1% and ~43.9%, respectively, as compared to those of AN/BA copolymer (37.1%) and AN/EHA copolymer (38.0%).

Study on the method for determination of the nuclear fuel elements burnout by the quantitative analysis of 148Nd

International Nuclear Information System (INIS)

Enoshita, Margarida

1978-01-01

The scope of present work to study the precision and accuracy of a method for separation and determination of the.stable isotope 148 Nd. The extraction chromatography and ion exchange techniques were used for the separation of fission products and uranium. Kieselguhr and di(2-ethyl-hexyl)phosphoric acid were used as inert support and stationary phase, respectively, in the steps of the separation procedure where the extraction chromatography technique was applied, and anionic resin mixed with Pb0 2 was used for the ion exchange operation. The behaviour of each element in the separation procedure was verified by means of radioactive tracers, namely, 147 Nd, 141 Ce and 137 Cs. Use was made of the thermal neutron activation analysis in order to determine the 148 Nd percentage recovered after the separation procedure was run. On the other hand, the radioactive isotope 147 Nd was used to find chemical yield achieved for the separation procedure. Student's t test applied to verify the accuracy of the method used whose acceptability was verified by using the criterion recommended by McFarren and also taking into account the suggestion proposed by Eckschlager. The precision of the method was verified by means of the standard deviation of the several determinations. (author)

First calorimetric determination of heat of extraction of 248Cm in a bi-phasic system

International Nuclear Information System (INIS)

Martin, Leigh R.; Zalupski, Peter R.

2011-01-01

This report presents a summary of the work performed to meet FCR and D level 2 milestone M21SW050201, 'Complete the first calorimetric determination of heat of extraction of 248Cm in a bi-phasic system'. This work was carried out under the auspices of the Thermodynamics and Kinetics FCR and D work package. To complement previous work undertaken under this work package we have extended out heat of extraction studies by di-2-ethyl-hexyl-phosphoric acid to curium. This report also details the heat of extraction of samarium in the same system. This work was performed to not only test the methodology but also to check for consistency with the heats of extraction obtained with those in the prior literature. The heat of extraction for samarium that was obtained in this study was -9.6 kJ mol-1, which is in reasonable agreement with the previously obtained value of -10.9 kJ mol-1. The curium heat of extraction was performed under two sets of conditions and the obtained heats of extraction were in reasonable agreement with each other at -16.0 ± 1.1 and -16.8 ± 1.5 kJ mol-1.

Uranium recovery from wet process phosphoric acid

International Nuclear Information System (INIS)

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

1981-01-01

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

A SrBPO5: Eu2+ phosphor for neutron imaging

International Nuclear Information System (INIS)

Sakasai, K.; Katagiri, M.; Toh, K.; Nakamura, T.

2001-01-01

A SrBPO 5 : Eu 2+ phosphor material has been investigated for neutron imaging. This phosphor showed photostimulated luminescence (PSL) by illumination of 635 nm laser light after X-ray irradiation. The spectral characteristics of the phosphor were similar to those of BaFBr: Eu 2+ , which is a commonly used phosphor of imaging plates. In addition, we found that this phosphor also showed PSL for neutron irradiation. It comes from the fact that it contains atomic boron in base matrix. Therefore, this phosphor can be used for neutron imaging without adding neutron sensitive materials such as Gd in commercially available neutron imaging plates. The PSL intensity and the neutron detection will be increased by using enriched boron instead of natural boron. (author)

Adsorptive removal of phthalate ester (Di-ethyl phthalate) from aqueous phase by activated carbon: a kinetic study.

Science.gov (United States)

Venkata Mohan, S; Shailaja, S; Rama Krishna, M; Sarma, P N

2007-07-19

Adsorptive studies were carried out on Di-ethyl phthalate (DEP) removal from aqueous phase onto activated carbon. Batch sorption studies were performed and the results revealed that activated carbon demonstrated ability to adsorb DEP. Influence of varying experimental conditions such as DEP concentration, pH of aqueous solution, and dosage of adsorbent were investigated on the adsorption process. Sorption interaction of DEP onto activated carbon obeyed the pseudo second order rate equation. Experimental data showed good fit with both the Langmuir and Freundlich adsorption isotherm models. DEP sorption was found to be dependent on the aqueous phase pH and the uptake was observed to be greater at acidic pH.

Extractants for uranium recovery from wet phosphoric acid

International Nuclear Information System (INIS)

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

1982-01-01

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

Stratified systems without organic solvent - new extraction type of macro- and microquantities of metal ions

International Nuclear Information System (INIS)

Dyogtev, M.I.; Alikina, E.N.; Popova, O.N.; Amindjanov, A.A.

2012-01-01

This article describes the results of studies on solubility in four component systems: di anti pyril methane-benzoic (salicylic) acid-HCl-H 2 O, hexyl di anti pyril methane-benzoic (salicylic) acid-HCl-H 2 O at 298 and 323 K. It is defined that stable stratification appears by addition of hydrochloric acid in the concentration range of 3.0-4.9 wt.% HCl. At substitution of di anti pyril methane on hexyl di anti pyril methane the wide range of stratification in the cut of hexyl di anti pyril methane-benzoic (salicylic) acid - 5 wt.% HCl is observes. The possibility of using of stratified systems for quantitative extraction of copper, cadmium, iron, thallium and tin is proposed.

Synthesis and photoluminescence study of rare earth activated phosphor Na2La2B2O7

International Nuclear Information System (INIS)

Nagpure, P.A.; Omanwar, S.K.

2012-01-01

The photoluminescence properties in UV and N-UV excitable range for the phosphors of Na 2 La 2 B 2 O 7 : RE (RE=Eu, Tb, Ce, Sm, Gd) are investigated. The solution combustion synthesis technique was employed for the synthesis of the phosphors Na 2 La 2 B 2 O 7 : RE. The photoluminescence measurements of the phosphors were carried out on a HITACHI F7000 Fluorescence Spectrophotometer. The PL and PL excitation (PLE) spectra indicate that the main emission wavelength of Na 2 La 2 B 2 O 7 : Eu are 591 and 615 nm, Na 2 La 2 B 2 O 7 : Ce shows dominating emission peak at 387 nm and Na 2 La 2 B 2 O 7 : Tb displays green emission at 493, 544, 593 and 620 nm at 254 nm excitation, while Na 2 La 2 B 2 O 7 : Sm shows the main emission peak wavelengths 566 and 604 nm at 405 nm excitation and Na 2 La 2 B 2 O 7 : Gd shows dominating emission peak at 312 nm at 274 nm excitation. These phosphors may provide a new kind of luminescent materials under ultraviolet and near ultraviolet excitation for various applications. - Highlights: ► We use the combustion technique for synthesis of Na 2 La 2 B 2 O 7 : RE phosphor. ► Phosphor Na 2 La 2 B 2 O 7 : Eu 3+ shows intense red emission under UV excitation. ► Phosphor Na 2 La 2 B 2 O 7 : Tb 3+ shows intense green emission under UV excitation. ► Phosphor Na 2 La 2 B 2 O 7 : Sm 3+ shows orange red emission under near UV excitation. ► Phosphors Na 2 La 2 B 2 O 7 : Ce 3+ and Na 2 La 2 B 2 O 7 : Gd 3+ show near UV and UVB emissions under UV excitation.

Iron halide mediated atom transfer radical polymerization of methyl methacrylate with N-Alkyl-2-pyridylmethanimine as the ligand

NARCIS (Netherlands)

Zhang, H.; Schubert, U.S.

2004-01-01

The controlled atom transfer radical polymerization (ATRP) of methyl methacrylate (MMA) catalyzed by iron halide/N-(n-hexyl)-2-pyridylmethanimine (NHPMI) is described. The ethyl 2-bromoisobutyrate (EBIB)-initiated ATRP with [MMA]0/[EBIB]0/[iron halide]0/[NHPMI]0 = 150/1/1/2 was better controlled in

Exposure to di-2-ethylhexyl terephthalate in a convenience sample of U.S. adults from 2000 to 2016.

Science.gov (United States)

Silva, Manori J; Wong, Lee-Yang; Samandar, Ella; Preau, James L; Calafat, Antonia M; Ye, Xiaoyun

2017-10-01

Di-2-ethylhexyl terephthalate (DEHTP), a structural isomer of di-2-ethylhexyl phthalate (DEHP), is a plasticizer used in a variety of commercial applications, but data on Americans' exposure to DEHTP do not exist. We investigated the exposure to DEHTP in a convenience group of U.S. adults by analyzing urine collected anonymously in 2000 (N = 44), 2009 (N = 61), 2011 (N = 81), 2013 (N = 92), and 2016 (N = 149) for two major DEHTP oxidative metabolites: mono-2-ethyl-5-carboxypentyl terephthalate (MECPTP) and mono-2-ethyl-5-hydroxyhexyl terephthalate (MEHHTP). For comparison, we also quantified the analogous DEHP metabolites mono-2-ethyl-5-hydroxyhexyl phthalate (MEHHP) and mono-2-ethyl-5-carboxypentyl phthalate (MECPP). We detected MECPTP, MEHHP, and MECPP in all samples collected in 2016 with geometric means of 13.1, 4.1, and 6.7 ng/mL, respectively; we detected MEHHTP in 91% of the samples (geometric mean = 3.1 ng/mL). Concentrations of MECPTP correlated well with those of MEHHTP (R 2  = 0.8, p  0.05) suggesting different sources of exposure to DEHP and DEHTP. We also evaluated the fraction of the metabolites eliminated in their free (i.e., unconjugated) form. The median percent of unconjugated species was lower for the DEHP metabolites (MECPP [45.5%], MEHHP [1.9%]) compared to the DEHTP metabolites (MECPTP [98.8%], MEHHTP [21.2%]). Contrary to the downward trend from 2000 to 2016 in urinary concentrations of MEHHP and MECPP, we observed an upward trend for MEHHTP and MECPTP. These preliminary data suggest that exposure to DEHTP may be on the rise. Nevertheless, general population exposure data using MEHHTP and MECPTP as exposure biomarkers would increase our understanding of exposure to DEHTP, one of the known DEHP alternatives.

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

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

Science.gov (United States)

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

2018-05-01

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

Spectral properties of Dy3+ doped ZnAl2O4 phosphor

Science.gov (United States)

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

2018-05-01

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

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

International Nuclear Information System (INIS)

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

2016-01-01

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

Di-(2-Ethylhexyl Phthalate and Autism Spectrum Disorders

Directory of Open Access Journals (Sweden)

Chiara Testa

2012-04-01

Full Text Available ASDs (autism spectrum disorders are a complex group of neurodevelopment disorders, still poorly understood, steadily rising in frequency and treatment refractory. Extensive research has been so far unable to explain the aetiology of this condition, whereas a growing body of evidence suggests the involvement of environmental factors. Phthalates, given their extensive use and their persistence, are ubiquitous environmental contaminants. They are EDs (endocrine disruptors suspected to interfere with neurodevelopment. Therefore they represent interesting candidate risk factors for ASD pathogenesis. The aim of this study was to evaluate the levels of the primary and secondary metabolites of DEHP [di-(2-ethylhexyl phthalate] in children with ASD. A total of 48 children with ASD (male: 36, female: 12; mean age: 11 ± 5 years and age- and sex-comparable 45 HCs (healthy controls; male: 25, female: 20; mean age: 12 ± 5 years were enrolled. A diagnostic methodology, based on the determination of urinary concentrations of DEHP metabolites by HPLC-ESI-MS (HPLC electrospray ionization MS, was applied to urine spot samples. MEHP [mono-(2-ethylhexenyl 1,2-benzenedicarboxylate], 6-OH-MEHP [mono-(2-ethyl-6-hydroxyhexyl 1,2-benzenedicarboxylate], 5-OH-MEHP [mono-(2-ethyl-5-hydroxyhexyl 1,2-benzenedicarboxylate] and 5-oxo-MEHP [mono-(2-ethyl-5-oxohexyl 1,2-benzenedicarboxylate] were measured and compared with unequivocally characterized, pure synthetic compounds (>98% taken as standard. In ASD patients, significant increase in 5-OH-MEHP (52.1%, median 0.18 and 5-oxo-MEHP (46.0%, median 0.096 urinary concentrations were detected, with a significant positive correlation between 5-OH-MEHP and 5-oxo-MEHP (r s=0.668, P<0.0001. The fully oxidized form 5-oxo-MEHP showed 91.1% specificity in identifying patients with ASDs. Our findings demonstrate for the first time an association between phthalates exposure and ASDs, thus suggesting a previously unrecognized role for

Luminescence properties of Na2Sr2Al2PO4Cl9:Sm3+ phosphor

Science.gov (United States)

Tamboli, Sumedha; Shahare, D. I.; Dhoble, S. J.

2018-04-01

A series of Sm3+ ions doped Na2Sr2Al2PO4Cl9 phosphors were synthesized via solid state synthesis method. Photoluminescence (PL) emission spectra were obtained by keeping excitation wavelength at 406 nm. Emission spectra show three emission peaks at 563 nm, 595 nm and 644 nm. The CIE chromaticity diagram shows emission colour of the phosphor in the orange-red region of the visible spectrum, indicating that the phosphor may be useful in preparing orange light-emitting diodes. Na2Sr2Al2PO4Cl9:Sm3+ phosphors were irradiated by γ-rays from a 60Co source and β-rays from a 90Sr source. Their thermoluminescence (TL) glow curves were obtained by Nucleonix 1009I TL reader. TL Trapping parameters such as activation energy of trapped electrons and order of kinetics were obtained by using Chen's peak shape method, Glow curve fitting method and initial rise method.

Fast detoxication of 2-chloro ethyl ethyl sulfide by p-type Ag_2O semiconductor nanoparticle-loaded Al_2O_3-based supports

International Nuclear Information System (INIS)

Ma, Meng-Wei; Kuo, Dong-Hau

2016-01-01

Highlights: • Detoxication of CWA surrogate of 2-chloro ethyl ethyl sulfide is investigated. • A small amount of Ag_2O on Al_2O_3-base support is sufficient to degrade 2-CEES. • Detoxication conversion >82% in 15 min is achieved for >2.5% Ag_2O/Na_2SiO_3/Al_2O_3. • Na_2SiO_3 modified Al_2O_3 to have the valley-like line pattern for depositing Ag_2O. • 2-CEES oxidation is initiated from the dominant electronic holes in p-type Ag_2O. - Abstract: p-type Ag_2O semiconductor nanoparticle-loaded Al_2O_3 or Na_2SiO_3/Al_2O_3 powders used for detoxicating the surrogate of sulfur mustard of 2-chloro ethyl ethyl sulfide (C_2H_5SCH_2CH_2Cl, 2-CEES) were investigated. Different amounts of Ag_2O and Na_2SiO_3 on catalyst supports were evaluated. Gas chromatography with a pulsed flame photometric detector (GC–PFPD) and gas chromatography coupled with a mass spectroscopy (GC–MS) were used to monitor and identify the catalytic reactions, together with reaction products analysis. The GC analyses showed that the decontamination of 2-CEES in isopropanol solvent for 15 min was above 82% efficiency for the 0.5% Na_2SiO_3/Al_2O_3 support deposited with a Ag_2O content above 2.5%. 2-(ethylthio)ethanol and 2-(ethylthio)ethanoic acid were identified as the major products after catalytic reactions. The electronic holes dominating in p-type Ag_2O is proposed to provide the key component and to initiate the catalytic reactions. The electronic hole-based detoxication mechanism is proposed.

2,6-Bis(9-ethyl-9H-carbazolylmethylenecyclohexanone

Directory of Open Access Journals (Sweden)

Abdullah M. Asiri

2009-10-01

Full Text Available The title compound, 2,6-bis(ethyl-9-ethyl-9H-carbazolylmethylenecyclohexanone has been synthesized by condensation of 9-ethylcarbazole-3-aldehyde and cyclohexanone in ethanol in the presence of pyridine. The structure of this new compound was confirmed by elemental analysis, IR, 1H NMR, 13C NMR and EI-MS spectral analysis.

Investigation of thermoluminescence and electron-vibrational interaction parameters in SrAl2O4:Eu2+, Dy3+ phosphors

International Nuclear Information System (INIS)

Pardhi, Shilpa A.; Nair, Govind B.; Sharma, Ravi; Dhoble, S.J.

2017-01-01

Combustion synthesis method was employed for the synthesis of green-emitting monoclinic SrAl 2 O 4 :Eu 2+ , Dy 3+ phosphors. The phase-purity of the prepared phosphors were examined using X-ray diffraction (XRD). The prepared phosphors exhibited green light emission with the peak centred at 510 nm, under 350 nm UV excitation. The excitation and emission spectra were analysed and the parameters of electron-vibrational interaction (EVI), such as the Huang–Rhys factor, effective phonon energy and zero-phonon line position were estimated using the spectrum fitting method. Thermoluminescence (TL) behaviour of the as-prepared phosphors were analysed for UV and 137 Cs γ-ray source irradiation. TL glow curves for UV-irradiated SrAl 2 O 4 :Eu 2+ , Dy 3+ phosphors were analysed. - Highlights: • Photoluminescence and thermoluminescence properties of SrAl 2 O 4 :Eu 2+ ,Dy 3+ phosphors were analysed. • Electron-vibrational interaction (EVI) parameters of SrAl 2 O 4 :Eu 2+ ,Dy 3+ phosphors were determined. • The phosphors are found to exhibit green light emission.

Distinguishing tautomerism in the crystal structure of (Z)-N-(5-ethyl-2,3-di-hydro-1,3,4-thiadiazol-2-ylidene) -4-methylbenzenesulfonamide using DFT-D calculations and {sup 13}C solid-state NMR

Energy Technology Data Exchange (ETDEWEB)

Li, Xiaozhou; Bond, Andrew D.; Johansson, Kristoffer E.; Van de Streek, Jacco, E-mail: jacco.vandestreek@sund.ku.dk [Department of Pharmacy, University of Copenhagen, Universitetsparken 2, Copenhagen DK-2100 (Denmark)

2014-08-01

The crystal structure of (Z)-N-(5-ethyl-2,3-di-hydro-1,3,4-thiadiazol-2-ylidene) -4-methylbenzenesulfonamide contains an imine tautomer, rather than the previously reported amine tautomer. The tautomers can be distinguished using dispersion-corrected density functional theory calculations and by comparison of calculated and measured {sup 13}C solid-state NMR spectra. The crystal structure of the title compound, C{sub 11}H{sub 13}N{sub 3}O{sub 2}S{sub 2}, has been determined previously on the basis of refinement against laboratory powder X-ray diffraction (PXRD) data, supported by comparison of measured and calculated {sup 13}C solid-state NMR spectra [Hangan et al. (2010 ▶). Acta Cryst. B66, 615–621]. The mol@@ecule is tautomeric, and was reported as an amine tautomer [systematic name: N-(5-ethyl-1,3,4-thia@@diazol-2-yl)-p-toluene@@sulfonamide], rather than the correct imine tautomer. The protonation site on the mol@@ecule’s 1,3,4-thia@@diazole ring is indicated by the inter@@molecular contacts in the crystal structure: N—H⋯O hydrogen bonds are established at the correct site, while the alternative protonation site does not establish any notable inter molecular inter@@actions. The two tautomers provide essentially identical Rietveld fits to laboratory PXRD data, and therefore they cannot be directly distinguished in this way. However, the correct tautomer can be distinguished from the incorrect one by previously reported qu@@anti@@tative criteria based on the extent of structural distortion on optimization of the crystal structure using dispersion-corrected density functional theory (DFT-D) calculations. Calculation of the {sup 13}C SS-NMR spectrum based on the correct imine tautomer also provides considerably better agreement with the measured {sup 13}C SS-NMR spectrum.

Color-tunable and highly thermal stable Sr_2MgAl_2_2O_3_6:Tb"3"+ phosphors

International Nuclear Information System (INIS)

Zhang, Haiming; Zhang, Haoran; Liu, Yingliang; Lei, Bingfu; Deng, Jiankun; Liu, Wei-Ren; Zeng, Yuan; Zheng, Lingling; Zhao, Minyi

2017-01-01

Tb"3"+ activated Sr_2MgAl_2_2O_3_6 phosphor was prepared by a high-temperature solid-state reaction route. The X-ray diffraction, scanning electron microscopy, and photoluminescence spectroscopy were used to characterize the as-prepared samples. The Sr_2MgAl_2_2O_3_6:Tb"3"+ phosphors show intense green light emission under UV excitation. The phosphor exhibit two groups of emission lines from about 370 to 700 nm, which originating from the characteristic "5D_3-"7F_J and "5D_4-"7F_J transitions of the Tb"3"+ ion, respectively. The cross-relaxation mechanism between the "5D_3 and "5D_4 emission was investigated and discussed. The emission colors of these phosphors can be tuned from bluish-green to green by adjusting the Tb"3"+ doping concentration. Furthermore, the thermal quenching temperature (T_1_/_2) is higher than 500 K. The excellent thermal stability and color-tunable luminescent properties suggest that the developed material is a promising green-emitting phosphor candidate for optical devices. - Highlights: • A Color-tunable emitting phosphor Sr_2MgAl_2_2O_3_6:Tb"3"+ was prepared successfully via high-temperature solid-state reaction. • The photoluminescence of Sr_2MgAl_2_2O_3_6:Tb"3"+ shows highly thermal stable. • The cross-relaxation mechanism between the "5D_3 and "5D_4 emission was investigated and discussed.

Preparation of mesoporous MnO2/C catalyst for n-hexyl acetate synthesis

International Nuclear Information System (INIS)

Yang Zeheng; Pan Yanmei; Mei Zhousheng; Zhang Weixin

2012-01-01

A mesoporous MnO 2 /C composite was prepared by impregnating self-made porous carbon spheres with manganese nitrate aqueous solution and subsequently reacting with KMnO 4 aqueous solution. It was characterized with X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), field emission scanning electron microscopy (FESEM), the Brunauer-Emmett-Teller (BET) surface area and the Barrett-Joyner-Halenda (BJH) pore size distribution. The as-prepared mesoporous MnO 2 /C composite was used as catalyst for the synthesis of n-hexyl acetate, and the effects of MnO 2 loading and esterification reaction parameters on the esterification rate were investigated. The results prove that MnO 2 loading has a significant effect on the catalytic activity and that the mesoporous MnO 2 /C composite exhibits high catalytic activity with an esterification rate of 96.42% under the conditions below: MnO 2 loading (73.09 wt%), catalyst dosage (0.1% in total weight), acetic acid/n-hexanol molar ratio (2:1), reaction temperature (130 °C) and reaction time (5 h).

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, (02; and -0.1.ltoreq..delta..ltoreq.0.4. In one embodiment, 32.ltoreq.y.ltoreq.2.15; and 3.ltoreq.z.ltoreq.3.2. Similarly, in another embodiment, 3.ltoreq.x.ltoreq.3.1; 22.15; and 2.8.ltoreq.z.ltoreq.3.2.

Synthesis, Analgesic and Anti-inflammatory Activities of 3- Ethyl-2 ...

African Journals Online (AJOL)

4(3H)-ones and evaluate them for their analgesic and anti-inflammatory activities. Methods: The compounds, 3-ethyl-2-substituted amino-quinazolin-4(3H)-ones, were synthesized by reacting the amino group of 3-ethyl-2-hydrazino ...

Development of Dy3+ activated K2MgP2O7 pyrophosphate phosphor for energy saving lamp

International Nuclear Information System (INIS)

Kohale, R.L.; Dhoble, S.J.

2013-01-01

Present work reports, synthesis of Dy 3+ activated K 2 MgP 2 O 7 pyrophosphate phosphor by using modified solid state diffusion that has been studied for its X-ray diffraction pattern (XRD). Furthermore, the chromaticity coordinate values were estimated from emission spectra of K 2 MgP 2 O 7 . The photoluminescence emission spectra of the phosphors having an excitation at around 351 nm (mercury free) showed two distinguishing bands centered at around 485 nm (blue) and 575 nm (yellow) corresponding to 4 F 9/2 → 6 H 15/2 and 4 F9 /2 → 6 H 13/2 transitions of Dy 3+ , respectively. These phosphors have strong absorption in the near UV region. K 2 MgP 2 O 7 pyrophosphate phosphor is suitable for color converter using UV light as the primary light source, which can be used as a blue/yellow phosphor excited by n-UV LED chip and mixed with other color emission phosphors to obtain white light. The 300–400 nm is Hg-free excitation (mercury excitation is 85% 254 nm wavelength of light and 15% other wavelengths), which is characteristic of solid-state lighting phosphors. Hence PL emission in trivalent dysprosium may be efficient photoluminescent materials for solid-state lighting phosphors. The intact study reveals that the present phosphor have promising applications in the lamp industry especially for solid state lighting (mercury-free excited lamp phosphor) and white light LED. -- Highlights: ► Dy 3+ activated pyrophosphate based phosphor prepared by modified solid state diffusion. ► PL emission spectrum of Dy 3+ ion under 351 nm excitation (Hg-free). ► PL emission at 485 nm (blue), 575 nm (yellow) emission. ► K 2 MgP 2 O 7 : Dy 3+ is expected to be a potential candidate for application in n-UV white LEDs and solid state lighting

(Z-Ethyl 3-(4-chlorophenyl-2-cyano-3-(2,6-difluorobenzamidoacrylate

Directory of Open Access Journals (Sweden)

Zhang Xiaoyan

2008-12-01

Full Text Available The title compound, C19H13ClF2N2O3, was prepared by the reaction of (Z-ethyl 3-amino-3-(4-chlorophenyl-2-cyanoacrylate and 2,6-difluorobenzoyl chloride. The dihedral angle between the chlorobenzene and fluorobenzene rings is 37.0 (1°. The ethyl group is disordered over two positions [occupancies = 0.52 (2:0.48 (2]. In addition to intramolecular N—H...O and N—H...F hydrogen bonds, the crystal packing shows the molecules to be connected by intermolecular C—H...O and C—H...N hydrogen bonds.

Structural and spectral properties of MgZnO2:Sm3+ phosphor

Science.gov (United States)

Rajput, Preasha; Sharma, Pallavi; Biswas, Pankaj; Kamni

2018-05-01

The samarium doped MgZnO2 phosphor was synthesized by the low-cost combustion method. The powder X-ray diffraction (XRD) analysis confirmed the crystallinity and phase purity of the phosphor. The lattice parameters were determined by indexing the diffraction peaks. The photoluminescence (PL) study revealed that the phosphor exhibited a broad excitation band in the UV region ranging between 200 to 350 nm. The 601 nm emission was ascribed to 4G5/2 to 6H7/2 transitions of the Sm3+ ion. The optical bandgap of MgZnO2:Sm3+ was obtained to be 3.56 eV. The phosphor can be projected as a useful material in X- and gamma-ray scintillators.

Solubility, density and excess molar volume of binary mixtures of aromatic compounds and common ionic liquids at T=283.15K and atmospheric pressure

OpenAIRE

Emilio J Gonzalez; Patricia Requejo; Filipa Maia; Ángeles Dominguez; Maria Eugénia Macedo

2015-01-01

In this work, the solubility of aromatic compounds (benzene, or toluene, or ethylbenzene, or o-xylene, or m-xylene, or p-xylene) in several ionic liquids (1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, or 1-hexyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide, or 1-ethyl-3-methylpyridinium bis(trifluoromethylsulfonyl)imide, or 1-propyl-3-methylpyridinium bis(trifluoromethylsulfonyl)imide, or 1-ethyl-3-methylpyridinium ethylsulfate, or 1-hexyl-3-methylimidazolium dicyana...

Luminescence properties of CdSiO3:Mn2+ phosphor

International Nuclear Information System (INIS)

Lei Bingfu; Liu Yingliang; Ye Zeren; Shi Chunshan

2004-01-01

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

Highly efficient transparent Zn2SiO4:Mn2+ phosphor film on quartz glass

International Nuclear Information System (INIS)

Seo, K.I.; Park, J.H.; Kim, J.S.; Kim, G.C.; Yoo, J.H.

2009-01-01

Highly efficient transparent Zn 2 SiO 4 :Mn 2+ film phosphors on quartz substrates were deposited by the thermal diffusion of sputtered ZnO:Mn film. They show a textured structure with some preferred orientations. Our film phosphor shows, for the best photoluminescence (PL) brightness, a green PL brightness of about 20% of a commercial Zn 2 SiO 4 :Mn 2+ powder phosphor screen. The film shows a high transmittance of more than 10% at the red-color region. The excellence in PL brightness and transmittance can be explained in terms of the textured crystal growth with a continuous gradient of Zn 2 SiO 4 : Mn 2+ crystals.

Rapid synthesis of spherical-shaped green-emitting MgGa2O4:Mn2+ phosphor via spray pyrolysis

International Nuclear Information System (INIS)

Choi, Sungho; Kim, Kyoungun; Moon, Young-Min; Park, Byung-Yoon; Jung, Ha-Kyun

2010-01-01

Simple, one-step synthesis of spherical-shaped powder phosphors with aqueous precursors via a spray pyrolysis method is reported. Green-emitting MgGa 2 O 4 :Mn 2+ phosphor with a controlled shape was successfully obtained by spraying under a reductive atmosphere (N 2 + H 2 carrier gas) without high-temperature post-heat treatment. In addition, the corresponding powder phosphors were well dispersed and showed a clean surface morphology compared to an existing cumbersome process using high-temperature post-annealing. The new method may help to prevent surface residual non-radiative defect sites. The result of highly luminescent and spherical morphology, non-aggregated powder phosphor by this procedure holds promise for a cost-effective and rapid synthesis process for conventional inorganic phosphors.

Processes for the production of rare earths from monazite (Paper No. 36)

International Nuclear Information System (INIS)

Murthy, T.K.S.

1979-01-01

A few typical cases are briefly described to illustrate different methods available for rare earth concentration and separation from mixed rare earths chloride obtained for monazite. In the case of cerium, rare earths chloride mixture is treated with sodium sulphate to precipitate rare earths as double sulphates from which hydroxide cake is prepared. The cake is dried to oxidise cerium. Trivalent rare earths are selectively leached and the product is treated with HNO 3 . The resulting ceric nitrate solution is purified by liquid-liquid extraction using TBP. The scrubbed extract is reduced with H 2 O 2 and cerous nitrate is recovered by evaporation. Lanthanum is first concentrated by selective precipitation of hydroxides from rare earths chloride using air-ammonia mixture. The hydroxyde cake is dissolved in HNO 3 and NH 4 NO 3 to get the double nitrate which is subjected to counter current crystallisation for purification. Europium is present at a concentration of 0.01% in the rare earths chloride. It is concentrated in several steps by liquid-liquid extraction using di-2-ethyl hexyl phosphoric acid. The product is purified by selective reduction and europium is obtained as europium sulphate. In the same solvent extraction process samarium and gadolinium are also concentrated to about 25%. They are further upgraded to above 90% purity by repetion of liquid-liquid extraction technique. Cerium, lanthanum and europium obtained by the above processes analyse > 99% as oxides. (M.G.B.)

Luminescence properties of Ca2 Ga2 SiO7 :RE phosphors for UV white-light-emitting diodes.

Science.gov (United States)

Jiao, Mengmeng; Lv, Wenzhen; Lü, Wei; Zhao, Qi; Shao, Baiqi; You, Hongpeng

2015-03-16

A series of Eu(2+) -, Ce(3+) -, and Tb(3+) -doped Ca2 Ga2 SiO7 phosphors is synthesized by using a high-temperature solid-state reaction. The powder X-ray diffraction and structure refinement data indicate that our prepared phosphors are single phased and the phosphor crystalizes in a tetrahedral system with the ${P\\bar 42m}$ (113) space group. The Eu(2+) - and Ce(3+) -doped phosphors both have broad excitation bands, which match well with the UV light-emitting diodes chips. Under irradiation of λ=350 nm, Ca2 Ga2 SiO7 :Eu(2+) and Ca2 Ga2 SiO7 :Ce(3+) , Li(+) have green and blue emissions, respectively. Luminescence of Ca2 Ga2 SiO7 :Tb(3+) , Li(+) phosphor varies with the different Tb(3+) contents. The thermal stability and energy-migration mechanism of Ca2 Ga2 SiO7 :Eu(2+) are also studied. The investigation results indicate that the prepared Ca2 Ga2 SiO7 :Eu(2+) and Ca2 Ga2 SiO7 :Ce(3+) , Li(+) samples show potential as green and blue phosphors, respectively, for UV-excited white-light-emitting diodes. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Luminescence in Eu2+ and Ce3+ doped SrCaP2O7 phosphors

Directory of Open Access Journals (Sweden)

K.N. Shinde

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

Photoluminescent properties of Sr2CeO4: Eu3+ and Sr2CeO4: Eu2+ phosphors suitable for near ultraviolet excitation

International Nuclear Information System (INIS)

Suresh, K.; Poornachandra Rao, N.V.; Murthy, K.V.R.

2014-01-01

Powder phosphors of 1 mol% Eu 3+ - and Eu 2+ -doped strontium cerium oxide (Sr 2 CeO 4 ) were synthesized by standard solid-state reaction method. Eu 3+ - and Eu 2+ -doped Sr 2 CeO 4 phosphors fired at 1100 ℃ for 2 h were analysed by X-ray diffraction (XRD) and photoluminescence (PL) techniques. The XRD patterns confirm that the obtained phosphors are a single phase of Sr 2 CeO 4 composed of orthorhombic structure. Room temperature PL excitation spectrum of air-heated Sr 2 CeO 4 : Eu phosphor has exhibited bands at 260, 280 and 350 nm. Whereas the excitation spectrum of Sr 2 CeO 4 : Eu phosphor heated under reducing (carbon) atmosphere exhibited single broadband range from 260 to 390 nm. The (PL) emission peaks of both the phosphors at 467 (blue), 537 (green) and 616 nm (red) generate white light under 260, 280 and 350 nm excitation wavelengths. The Commission International de l'Eclairage (CIE) colour coordinates conforms that these phosphors emitting white light. The results reveal that these phosphors are multifunctional phosphors which emit white light under these excitations that they could be used as white components for display and lamp devices and as well as possible good light-conversion phosphor LEDs under near-ultraviolet (nUV) chip. (author)

Bluish-green color emitting Ba2Si3O8:Eu2+ ceramic phosphors for white light-emitting diodes.

Science.gov (United States)

Xiao, F; Xue, Y N; Zhang, Q Y

2009-10-15

This paper reports on the structural and optical properties of Eu(2+) activated Ba(2)Si(3)O(8) ceramic phosphors synthesized by a sol-gel method. The ceramic phosphors have been characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and fluorescence measurements. The structural characterization results suggest that the as-prepared phosphors are of single phase monoclinic Ba(2)Si(3)O(8) with rod-like morphology. A broad excitation band ranging from 300 to 410 nm matches well with the ultraviolet (UV) radiation of light-emitting diodes (LEDs). Upon 380 nm UV light excitation, these phosphors emit bluish-green emission centered at 500 nm with color coordination (x=0.25, y=0.40). All the obtained results indicate that the Ba(2)Si(3)O(8):Eu(2+) ceramic phosphors are promising bluish-green candidates for the phosphor-converted white LEDs.

Preparation of MAl 2 O 4 : Eu 2+ , Sm 3+ (M = Ca, Sr, Ba) Phosphors ...

African Journals Online (AJOL)

A series of MAl2O4: Eu2+, Sm3+ (M = Ca, Sr, Ba) phosphors was prepared by the combustion method, and the influence of these alkaline earth metals on the structure and luminescent performances for these phosphors was investigated. A relationship was established between their composition, crystallization capacity and ...

Concentration quenching of Eu2+ in a thermal-stable yellow phosphor Ca2BO3Cl:Eu2+ for LED application

International Nuclear Information System (INIS)

Zhang Xinguo; Zhang Jilin; Dong Zhiyue; Shi Jianxin; Gong Menglian

2012-01-01

A piece-shaped phosphor Ca 2 BO 3 Cl: Eu 2+ was synthesized by solid-state reaction method. This phosphor exhibited wide absorption in ultra-violet and visible range, and bright yellow emission band centering at 570 nm. The concentration quenching mechanism was verified to be a dipole–dipole interaction, and its critical transfer distance was about 17 Å by both calculated crystal structural method and experimental spectral method. This phosphor has a good thermal stability with a quenching temperature (T 1/2 ) of 200 °C. Yellow and white LEDs were fabricated with this phosphor and near UV chips, and the yellow LED has a high color purity of 97.0% and promising current tolerant property, while the white LED shows a luminous efficiency of 11.68 lm/W. - Highlights: ► Broadband excitable and strong yellow-emitting Ca 2 BO 3 Cl: Eu 2+ phosphor is obtained by solid state reaction. ► Concentration quenching mechanism of Ca 2 BO 3 Cl: Eu 2+ is dipole–dipole interaction. ► Quenching temperature (T 1/2 ) of Ca 2 BO 3 Cl: Eu 2+ is at 200 °C. ► As synthesized material can be used for LED phosphor application.

Photovoltaic characterization of hybrid solar cells using surface modified TiO2 nanoparticles and poly(3-hexyl)thiophene

International Nuclear Information System (INIS)

Guenes, Serap; Marjanovic, Nenad; Nedeljkovic, Jovan M; Sariciftci, Niyazi Serdar

2008-01-01

We report on the photovoltaic performance of bulk heterojunction solar cells using novel nanoparticles of 6-palmitate ascorbic acid surface modified TiO 2 as an electron acceptor embedded into the donor poly(3-hexyl)thiophene (P3HT) matrix. Devices were fabricated by using P3HT with varying amounts of red TiO 2 nanoparticles (1:1, 1:2, 1:3 w-w ratio). The devices were characterized by measuring current-voltage characteristics under simulated AM 1.5 conditions. Incident photon to current efficiency (IPCE) was spectrally resolved. The nanoscale morphology of such organic/inorganic hybrid blends was also investigated using atomic force microscopy (AFM).

Novel one-pot process for the synthesis of ethyl 2-imino-4-methyl-2,3-dihydrothiazole-5-carboxylates

Directory of Open Access Journals (Sweden)

Beyzaei Hamid

2015-01-01

Full Text Available A facile one-pot two-step process for the synthesis of ethyl 2-imino-4-methyl-2,3-dihydrothiazole-5-carboxylates via the cyclocondensation of ethyl 2-thiocyanatoacetoacetate with a variety of hydrazine and hydrazide derivatives has been developed. Ethyl 2-thiocyanatoacetoacetate itself has been synthesized as intermediate from the reaction of ethyl 2-chloroacetoacetate with potassium thiocyanate (KSCN. The molecular structures of these newly synthesized compounds were elucidated on the basis of elemental analysis and spectral data.

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

International Nuclear Information System (INIS)

Tu Dong; Liang Yujun; Liu Rong; Li Daoyi

2011-01-01

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

Ca8NaY(PO4)6F2:Eu2+,Mn2+: a potential color-tunable phosphor for white LEDs applications

International Nuclear Information System (INIS)

Fen, Zhang; Wanjun, Tang

2015-01-01

Eu 2+ - and/or Mn 2+ -activated Ca 8 NaY(PO 4 ) 6 F 2 phosphors have been prepared via a combustion-assisted synthesis route. The powder X-ray diffraction measurement revealed that Ca 8 NaY(PO 4 ) 6 F 2 crystallized in a hexagonal crystal system with the space group P6 3 /m (176). The photoluminescence spectrum of the Eu 2+ single-doped phosphor shows a broad blue emission band peaking at 451 nm under the excitation of UV irradiation. The Eu 2+ -/Mn 2+ -codoped phosphors show a blue emission band and an orange emission band, and the corresponding CIE coordinates intuitively indicate the tunable colors from blue to yellow area. The energy transfer from the Eu 2+ to Mn 2+ ions is demonstrated to be a quadrupole-quadrupole mechanism in terms of the experimental results and analysis of PL spectra and decay curves of the phosphors. The developed phosphors can be efficiently excited in the UV region and exhibit a tunable white-light emission, making them attractive as single-component white-light-emitting conversion phosphors for UV-based white LEDs. (orig.)

Solubility of carbon dioxide in the low-viscosity ionic liquid 1-hexyl-3-methylimidazolium tetracyanoborate

NARCIS (Netherlands)

Mota Martinez, M.T.; Althuluth, M.A.M.; Kroon, M.C.; Peters, C.J.

2012-01-01

The solubility of carbon dioxide (CO2) in a new low-viscosity and non-fluorinated ionic liquid, 1-hexyl-3-methylimidazolium tetracyanoborate ([hmim][TCB]), has been studied experimentally using a synthetic method. Bubble point pressures (up to 12.34 MPa) of the system CO2 + [hmim][TCB] are reported

Study of the volatile compounds from plum (Prunus domestica L. cv. Horvin and estimation of their contribution to the fruit aroma

Directory of Open Access Journals (Sweden)

Jorge Antonio Pino

2012-03-01

Full Text Available Simultaneous Distillation-Extraction (SDE and headspace-solid phase microextraction (HS-SPME combined with GC-FID and GC-MS were used to analyze volatile compounds from plum (Prunus domestica L. cv. Horvin and to estimate the most odor-active compounds by application of the Odor Activity Values (OAV. The analyses led to the identification of 148 components, including 58 esters, 23 terpenoids, 14 aldehydes, 11 alcohols, 10 ketones, 9 alkanes, 7 acids, 4 lactones, 3 phenols, and other 9 compounds of different structures. According to the results of SDE-GC-MS, SPME-GC-MS and OAV, ethyl 2-methylbutanoate, hexyl acetate, (E-2-nonenal, ethyl butanoate, (E-2-decenal, ethyl hexanoate, nonanal, decanal, (E-β-ionone, Γ-dodecalactone, (Z-3-hexenyl acetate, pentyl acetate, linalool, Γ-decalactone, butyl acetate, limonene, propyl acetate, Δ-decalactone, diethyl sulfide, (E-2-hexenyl acetate, ethyl heptanoate, (Z-3-hexenol, (Z-3-hexenyl hexanoate, eugenol, (E-2-hexenal, ethyl pentanoate, hexyl 2-methylbutanoate, isopentyl hexanoate, 1-hexanol, Γ-nonalactone, myrcene, octyl acetate, phenylacetaldehyde, 1-butanol, isobutyl acetate, (E-2-heptenal, octadecanal, and nerol are characteristic odor active compounds in fresh plums since they showed concentrations far above their odor thresholds.

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

Acetate reduction synthesis of Sr2Si5N8:Eu2+ phosphor and its luminescence properties

International Nuclear Information System (INIS)

Piao Xianqing; Machida, Ken-ichi; Horikawa, Takashi; Yun Bonggoo

2010-01-01

A novel synthesis method was developed for the efficient red phosphor, Eu 2+ -activated Sr 2 Si 5 N 8 , by employing the strontium acetate as both the reducing agent and strontium source. The phase purity of final product was strongly dependent on the heating rate of the precursors. Sr 2 Si 5 N 8 :Eu 2+ (2 at%) phosphor presented a broadband excitation spectrum in the range 300-500 nm, matching well with the blue emission (400/460 nm) of current InGaN light-emitting diodes (LEDs). The red emission peaking at 619 nm gave the relatively high (about 155%) intensity compared with the Y 3 Al 5 O 12 (YAG) (P46-Y3) standard phosphor. In addition, the saturated chromatic coordinates (0.638, 0.359) allowed it a promising candidate as a red phosphor in white LEDs application for illumination or display.

Radiochemical synthesis of etomoxir

Energy Technology Data Exchange (ETDEWEB)

Abbas, Hafiz G. [Institute of Nuclear Medicine and Oncology (INMOL), New Campus Road, Lahore (Pakistan); Yunus, M. [University of the Punjab, New Campus Road, Lahore (Pakistan); Feinendegen, Ludwig E., E-mail: feinendegen@gmx.ne [Department of Nuclear Medicine, Heinrich-Heine University Duesseldorf, Wannental 45, 88131 Lindau (Germany)

2011-02-15

Sodium 2-{l_brace}6-(4-chlorophenoxy)hexyl{r_brace}oxirane-2-carboxylate (Etomoxir) inhibits transport of fatty acids via the carnitine shuttle into mitochondria of muscle cells and prevents long chain fatty acids from providing energy through {beta}-oxidation especially for muscle contraction. The objective of this synthesis is to develop a method for radioiodination of Etomoxir in order to explore its potential in diagnostic metabolic studies and molecular imaging. Thus, a method is described for the radiochemical synthesis and purification of ethyl 2-{l_brace}6-(4-[{sup 131}I]iodophenoxy)hexyl{r_brace}oxirane-2-carboxylate (3) and 2-{l_brace}6-(4-[{sup 131}I]iodo-phenoxy)hexyl{r_brace}oxirane-2-carboxylic acid (4). For the synthesis of these new agents, ethyl 2-{l_brace}6-(4-bromophenoxy)hexyl{r_brace}oxirane-2-carboxylate (1) and 2-{l_brace}6-(4-bromophenoxy)hexyl{r_brace}oxirane-2-carboxylic acid (2) were refluxed with [{sup 131}I]NaI in the presence of anhydrous acetone at a temperature of 80 {sup o}C and 90 {sup o}C for a period of 3-4 hours, respectively. The method of radiolabeling, based on the nucleophilic exchange reaction, resulted in a radiochemical yield of 43% and 67% for compounds 3 and 4, respectively. This paper reports on the labeling of etomoxir with radioiodine as {sup 124}I labeled etomoxir may be of great importance in molecular imaging.

Rare Earth Free Zn3V2O8 Phosphor with Controlled Microstructure and Its Photocatalytic Activity

Directory of Open Access Journals (Sweden)

Hom Nath Luitel

2013-01-01

Full Text Available Microsphere of rare earth free phosphor, Zn3V2O8, with broadband yellowish white emission was synthesized by combustion route and compared with the hydrothermal, sol-gel, and solid state reaction methods. The phosphor samples were characterized by X-ray diffraction and scanning electron microscopy. UV-visible absorption and photoluminescence (PL emission and excitation spectra were investigated for these phosphors. Zn3V2O8 phosphor containing 10 mol% of H3BO3 flux exhibited enhanced PL emission showing broadband from 450 nm to 750 nm. Effect of stoichiometry of Zn and V on the host lattice and its effect on the PL emission spectra were studied. Series of Mg3V2O8, Ca3V2O8, and Sr3V2O8 phosphors were also synthesized and compared to the Zn3V2O8 phosphor in terms of PL emission and internal quantum yield, and it was found that Zn3V2O8 is the most efficient phosphor among the other phosphors studied with quantum yield of 60%. The visible light irradiated photocatalytic activity of these phosphors was investigated and it was found that the hydrothermal Zn3V2O8 exhibited enhanced activity.

Correlation of Structure, Tunable Colors, and Lifetimes of (Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ Phosphors

OpenAIRE

Qidi Xie; Bowen Li; Xin He; Mei Zhang; Yan Chen; Qingguang Zeng

2017-01-01

(Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ phosphors were prepared via a high temperature solid-state reaction method. The correlation of phase structure, optical properties and lifetimes of the phosphors are investigated in this work. For the (Sr, Ca)Al2O4:Eu2+, Dy3+ phosphors, the different phase formation from monoclinic SrAl2O4 phase to hexagonal SrAl2O4 phase to monoclinic CaAl2O4 phase was observed when the Ca content increased. The emission color of SrAl2O4:Eu2+, Dy3+ phosphors varied from green to ...

Increased Urinary Phthalate Levels in Women with Uterine Leiomyoma: A Case-Control Study.

Science.gov (United States)

Kim, Young Ah; Kho, Younglim; Chun, Kyoung Chul; Koh, Jae Whoan; Park, Jeong Woo; Bunderson-Schelvan, Melisa; Cho, Yoon Hee

2016-12-15

We assessed the urinary concentration of 16 phthalate metabolites in 57 women with and without uterine leiomyoma ( n = 30 and 27; respectively) to determine the association between phthalate exposure and uterine leiomyoma. To evaluate exposure to di-(2-ethylhexyl) phthalate (DEHP); we calculated the molar sum of DEHP metabolites; ∑3-DEHP (combining mono-(2-ethylhexyl) phthalate (MEHP); mono-(2-ethyl-5-hydroxyhexyl) phthalate (MEHHP); and mono-(2-ethyl-5-oxohexyl) phthalate); ∑4-DEHP (∑3-DEHP plus mono-(2-ethyl-5-carboxypentyl) phthalate); and ∑5-DEHP (∑4-DEHP plus mono (2-(carboxylmethyl)hexyl) phthalate (2cx-MMHP)). The log transformed urinary levels of MEHP; MEHHP; 2cx-MMHP; ∑3-DEHP; ∑4-DEHP; and ∑5-DEHP in the leiomyoma group were significantly higher than those of controls. When we adjusted for age; waist circumference; and parity using multiple logistic regression analyses; we found log ∑3-DEHP (OR = 10.82; 95% CI = 1.25; 93.46) and ∑4-DEHP (OR = 8.78; 95% CI = 1.03; 75.29) were significantly associated with uterine leiomyoma. Our findings suggest an association between phthalate exposure and uterine leiomyoma. However; larger studies are needed to investigate potential interactions between phthalate exposure and uterine leiomyoma.

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

Temperature dependent luminescence and energy transfer properties of Na2SrMg(PO4)2:Eu2+, Mn2+ phosphors.

Science.gov (United States)

Geng, Dongling; Shang, Mengmeng; Zhang, Yang; Lian, Hongzhou; Lin, Jun

2013-11-21

Eu(2+) singly and Eu(2+)/Mn(2+) co-doped Na2SrMg(PO4)2 (NSMP) phosphors have been prepared via a high-temperature solid-state reaction process. Upon UV excitation of 260-360 nm, the NSMP:xEu(2+) phosphors exhibit a violet band located at 399 nm and a blue band centered at 445 nm, which originate from Eu(2+) ions occupying two different crystallographic sites: Eu(2+)(I) and Eu(2+)(II), respectively. Excitation wavelengths longer than 380 nm can selectively excite Eu(2+)(II) to emit blue light. Energy transfer processes in the Eu(2+)(I)-Eu(2+)(II) and Eu(2+)-Mn(2+) pairs have been observed and investigated by luminescence spectra and decay curves. The emission color of as-prepared samples can be tuned by changing the relative concentrations of Eu(2+) and Mn(2+) ions and adjusting the excitation wavelength. Under UV excitation of 323 nm, the absolute quantum yield of NSMP:0.005Eu(2+) is 91%, which is higher than most of the other Eu(2+)-doped phosphors reported previously. The temperature dependent luminescence properties and decay curves (4.3-450 K) of NSMP:Eu(2+) and NSMP:Eu(2+), Mn(2+) phosphors have been studied in detail. Thermal quenching of Eu(2+) has been observed while the emission band of Mn(2+) shows a blue-shift and an abnormal increase of intensity with increasing temperature. The unusual thermal quenching behavior indicates that the NSMP compound can serve as a good lattice host for Mn(2+) ions which can be used as a red-emitting phosphor. Additionally, the lifetimes for Eu(2+)(I) and Eu(2+)(II) increase with increasing temperatures.

Facile preparation and formation mechanism of Sr2Si5N8:Eu2+ red-emitting phosphors

Science.gov (United States)

Wang, Yang; Wang, Yunli; Wang, Ming; Shao, Yiran; Zhu, Yingchun

2018-05-01

The red-emitting Sr2Si5N8:Eu2+ phosphors have been synthesized in a new facile process using (oxy)nitride precursors by inductive calcination under N2 atmosphere at ordinary pressure. Different from the prevailing methods, lower cost raw materials, simpler pretreatment, without harsh conditions and a shorter reaction time are achieved. It was found that red-emitting Sr2Si5N8:Eu2+ phosphors were synthesized with high crystallinity and purity after 1 h inductive calcination. The formation mechanism was characterized by XRD, SEM, TEM and Fluorescence microscopy. It was demonstrated that a hexagonal mesophase of Sr-doped α-Si3N4 was primarily formed in the reaction process, which transformed into the final product of the orthorhombic Sr2Si5N8:Eu2+ phosphors. During the reaction process, the color of the samples transforms from greenish-yellow to orange and eventually to red. The as-prepared phosphors have a wide excitation in the range of 250 ∼ 570 nm which matches blue light chips and give a red-light emission peaking at 610 nm. The results indicate a promising prospect for a simple, efficient and inexpensive way to prepare Sr2Si5N8:Eu2+ phosphors for blue/UV-based warm-white LEDs and other fluorescent applications.

Photovoltaic characterization of hybrid solar cells using surface modified TiO{sub 2} nanoparticles and poly(3-hexyl)thiophene

Energy Technology Data Exchange (ETDEWEB)

Guenes, Serap [Yildiz Technical University, Faculty of Arts and Science, Department of Physics, Davutpasa Campus, 34220, Esenler, Istanbul (Turkey); Marjanovic, Nenad [Plastic electronic GmbH, Rappetsederweg 28, A-4040 Linz (Austria); Nedeljkovic, Jovan M [Vinca Institute of Nuclear Sciences, PO Box 522, 11001 Belgrade (Serbia); Sariciftci, Niyazi Serdar [Linz Institute for Organic Solar Cells (LIOS), Physical Chemistry, Johannes Kepler University Linz, Altenberger Strasse 69, A-4040, Linz (Austria)], E-mail: sgunes@yildiz.edu.tr

2008-10-22

We report on the photovoltaic performance of bulk heterojunction solar cells using novel nanoparticles of 6-palmitate ascorbic acid surface modified TiO{sub 2} as an electron acceptor embedded into the donor poly(3-hexyl)thiophene (P3HT) matrix. Devices were fabricated by using P3HT with varying amounts of red TiO{sub 2} nanoparticles (1:1, 1:2, 1:3 w-w ratio). The devices were characterized by measuring current-voltage characteristics under simulated AM 1.5 conditions. Incident photon to current efficiency (IPCE) was spectrally resolved. The nanoscale morphology of such organic/inorganic hybrid blends was also investigated using atomic force microscopy (AFM)

High colour purity single-phased full colour emitting white LED phosphor Sr2V2O7:Eu3+

International Nuclear Information System (INIS)

Zhou Zhi; Zhou Nan; He Zhangxing; Liu Suqin; Liu Younian; Tian Ziwei; Wang Nanfang; Mao Zhiyong; Hintzen, H T

2013-01-01

Single-phased white-light-emitting phosphor Sr 2 V 2 O 7 :Eu 3+ was successfully synthesized by the solid-state method. The result of x-ray diffraction analysis indicated that the obtained phosphor has the same crystal structure as that of Sr 2 V 2 O 7 . The synthesized Sr 2 V 2 O 7 :Eu 3+ was combined with near-UV light (365 nm) chips and then assembled into ligtht-emitting diodes (LED) devices, which generated white light with colour coordinates of (0.324, 0.317). The white light was generated from yellow-green and red emissions, which should be attributed to the host Sr 2 V 2 O 7 and dopant Eu ions, respectively. The effects of the concentration of Eu ions and charge compensation on the emission intensity were carefully investigated. The results show that the energy migrates from the host to the dopant and also that Li 2 CO 3 should be the best charge compensator for this single-phased phosphor. In addition, the colour rendering index and luminescence efficiency of the fabricated LED devices with Sr 1.90 V 2 O 7 :0.10Eu 3+ phosphor were 91 and 32 lm W -1 , respectively, suggesting that Sr 1.90 V 2 O 7 :0.10Eu 3+ phosphor is a potential candidate for the phosphor-converted white-light-emitting diodes with near-UV chips.

Long lasting behavior of Gd2O2S:Eu3+ phosphor synthesized by hydrothermal routine

International Nuclear Information System (INIS)

Hang Tao; Liu Qun; Mao Dali; Chang Chengkang

2008-01-01

This paper reports the detailed preparation process and afterglow properties of Eu 3+ activated long lasting Gd 2 O 2 S phosphor by hydrothermal routine. Rod-like Gd(OH) 3 were firstly synthesized by hydrothermal method to serve as the precursor. Long lasting Gd 2 O 2 S:Eu 3+ ,Ti 4+ ,Mg 2+ phosphor was obtained by calcinating the precursor with co-activators and S powder. It was found from the results that the hydrothermally prepared Gd(OH) 3 revealed a rod-like morphology, while the calcinated Gd 2 O 2 S:Eu 3+ ,Ti 4+ ,Mg 2+ phosphor showed a round granular shape. The morphological change can be explained by the etching effect of the melt that was formed by the carbonate and S powder during the high temperature calcination. The obtained Gd 2 O 2 S:Eu 3+ ,Ti 4+ ,Mg 2+ phosphor produced a red emission upon 243 nm UV excitation, which is a typical emission of Eu 3+ from 5 D j to 7 F j states. Long lasting behavior was observed after the UV source was switched off, due to the formation of electron traps with suitable trap depth within the matrix by the codoped Ti 4+ and Mg 2+ ions

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)

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.

Synthesis and photoluminescence properties of Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped Ca{sub 2}ZnWO{sub 6} phosphors for phosphor converted LED

Energy Technology Data Exchange (ETDEWEB)

Dabre, K.V. [Department of Physics, Arts, Commerce and Science College, Koradi, Nagpur-441111, Maharashtra (India); Dhoble, S.J., E-mail: sjdhoble@rediffmail.com [Department of Physics, R.T.M. Nagpur University, Nagpur-440033, Maharashtra (India)

2014-06-01

In this work, we report on the synthesis and photoluminescence (PL) properties of rare earth (Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+}) doped double perovskite tungstate Ca{sub 2}ZnWO{sub 6} phosphor. The phosphors were synthesized by two step modified solid state method. Phase purity and formation of phosphor were confirmed by XRD technique. PL spectra of Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped phosphor show intense emission peaks in red region at 615, 604 and 650 nm respectively, upon the visible excitation of 466 nm (Eu{sup 3+}), 410 nm (Sm{sup 3+}) and 491 nm (Pr{sup 3+}). The CIE coordinates of the phosphors are in the yellow (Sm{sup 3+} doped sample) and orange (Eu{sup 3+} and Pr{sup 3+} doped sample) regions near the edge of color space which confirms their applicability in LEDs. -- Highlights: •Eu{sup 3+}, Sm{sup 3+} and Pr{sup 3+} doped and undoped samples of Ca{sub 2}ZnWO{sub 6} phosphor synthesized by Solid state method. •The phosphors have intense excitation in violet and blue region of visible spectrum. •Phosphors show intense emission peaks in red region. •CIE coordinates of phosphors are lie in yellow (Sm{sup 3+} doped phosphor) and orange (Eu{sup 3+} and Pr{sup 3+} doped phosphor) region near to edge of color space.

Impact of Biodiesel Blends and Di-Ethyl-Ether on the Cold Starting Performance of a Compression Ignition Engine

Directory of Open Access Journals (Sweden)

Adrian Clenci

2016-04-01

Full Text Available The use of biodiesel fuel in compression ignition engines has the potential to reduce CO2, which can lead to a reduction in global warming and environmental hazards. Biodiesel is an attractive fuel, as it is made from renewable resources. Many studies have been conducted to assess the impact of biodiesel use on engine performances. Most of them were carried out in positive temperature conditions. A major drawback associated with the use of biodiesel, however, is its poor cold flow properties, which have a direct influence on the cold starting performance of the engine. Since diesel engine behavior at negative temperatures is an important quality criterion of the engine’s operation, one goal of this paper is to assess the starting performance at −20 °C of a common automotive compression ignition engine, fueled with different blends of fossil diesel fuel and biodiesel. Results showed that increasing the biodiesel blend ratio generated a great deterioration in engine startability. Another goal of this study was to determine the biodiesel blend ratio limit at which the engine would not start at −20 °C and, subsequently, to investigate the impact of Di-Ethyl-Ether (DEE injection into the intake duct on the engine’s startability, which was found to be recovered.

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

International Nuclear Information System (INIS)

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

2016-01-01

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

Combustion synthesis of CaSc2O4:Ce3+ nano-phosphors in a closed system

International Nuclear Information System (INIS)

Peng Wenfang; Zou Shaoyu; Liu Guanxi; Xiao Quanlan; Zhang Rui; Xie Lijuan; Cao Liwei; Meng Jianxin; Liu Yingliang

2011-01-01

Highlights: → CaSc 2 O 4 :Ce 3+ nano-phosphors can be prepared by a single-step combustion method. → The ignition temperature is the lowest in the combustion synthesis of Ce 3+ /Eu 2+ doped phosphors. → The as-prepared nano-phosphors give a uniform particle size in the range of 15-20 nm and have highly dispersity and fluorescence intensity. → It is a convenient method for preparation of monodispersed oxide nano-phosphors, especially those being sensitive to air at high temperature. - Abstract: The CaSc 2 O 4 :Ce 3+ nano-phosphors were successfully prepared by a single-step combustion method at an ignition temperature as low as 200 deg. C in a closed autoclave using glycine as a fuel and PEG4000 as a dispersant. The samples were characterized by X-ray diffraction (XRD), photoluminescence (PL) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscope (TEM). The results revealed that CaSc 2 O 4 :Ce 3+ nano-phosphors can be conveniently prepared at an ignition temperature as low as 200 deg. C, which was much lower than that in the ordinary combustion methods. The optimized ignition temperature was 220 deg. C. The CaSc 2 O 4 :Ce 3+ nano-phosphors give a uniform particle size in the range of 15-20 nm. The low ignition temperature and the addition of PEG4000 dispersant play important roles in the formation of small sized nanoparticles. The as-prepared nano-phosphors were incompact aggregates, but highly dispersed nano-phosphors can be obtained after further ultrasonic treatment. The CaSc 2 O 4 :Ce 3+ nano-phosphors give satisfactory luminescence characteristic benefiting from the closed circumstance, in which cerium atoms can be isolated from the oxidizing atmosphere and non-fluorescent Ce 4+ ions can be ruled out. The present highly dispersed CaSc 2 O 4 :Ce 3+ nano-phosphors with efficient fluorescence are promising in the field of biological labeling, and the present low temperature combustion method is facile and convenient and can

Thermoluminescence dosimetric characteristics of thulium doped ZnB2O4 phosphor

International Nuclear Information System (INIS)

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

2014-01-01

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

Luminescence characteristics of Sr{sub 1-x}Ba{sub x}Si{sub 2}O{sub 2}N{sub 2}:Eu{sup 2+} phosphors for white light emitting diodes

Energy Technology Data Exchange (ETDEWEB)

Anoop, G.; Cho, I.H.; Suh, D.W.; Yoo, J.S. [Display Materials Laboratory, School of Chemical Engineering and Materials Science, Chung-Ang University, Heukseok-Dong 221, Dongjak-gu, Seoul 156-756 (Korea, Republic of)

2012-12-15

Sr{sub 1-x}Ba{sub x}Si{sub 2}O{sub 2}N{sub 2}:Eu{sup 2+} phosphors were synthesized using high temperature solid state reaction. The effect of Ba incorporation on the structural and luminescence characteristics of SrSi{sub 2}O{sub 2}N{sub 2}:Eu{sup 2+} phosphors were studied. The phosphors were crystallized in triclinic crystal structure and the cell volume increases monotonically with Ba addition. The PL emission peak wavelength red shifts with Ba up to x = 0.50 beyond which no red shift is observed. The XPS analysis shows that nitrogen is being incorporated into the host lattice along with Ba addition up to x = 0.50. The as synthesized phosphors show high thermal stability. Phosphor converted light emitting diodes were realized using Sr{sub 1-x}Ba{sub x}Si{sub 2}O{sub 2}N{sub 2}:Eu{sup 2+} phosphors (x = 0 and x = 0.40) showing luminance efficacies of 108 and 101 lm W{sup -1}. The CIE chromaticity coordinates of Sr{sub 1-x}Ba{sub x}Si{sub 2}O{sub 2}N{sub 2}:Eu (x = 0 and x = 0.40) phosphors. (Copyright copyright 2012 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Correlation of Structure, Tunable Colors, and Lifetimes of (Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ Phosphors

Science.gov (United States)

Xie, Qidi; Li, Bowen; He, Xin; Zhang, Mei; Chen, Yan; Zeng, Qingguang

2017-01-01

(Sr, Ca, Ba)Al2O4:Eu2+, Dy3+ phosphors were prepared via a high temperature solid-state reaction method. The correlation of phase structure, optical properties and lifetimes of the phosphors are investigated in this work. For the (Sr, Ca)Al2O4:Eu2+, Dy3+ phosphors, the different phase formation from monoclinic SrAl2O4 phase to hexagonal SrAl2O4 phase to monoclinic CaAl2O4 phase was observed when the Ca content increased. The emission color of SrAl2O4:Eu2+, Dy3+ phosphors varied from green to blue. For the (Sr, Ba)Al2O4:Eu2+, Dy3+ phosphors, different phase formation from the monoclinic SrAl2O4 phase to the hexagonal BaAl2O4 phase was observed, along with a shift of emission wavelength from 520 nm to 500 nm. More interestingly, the decay time of SrAl2O4:Eu2+, Dy3+ changed due to the different phase formations. Lifetime can be dramatically shortened by the substitution of Sr2+ with Ba2+ cations, resulting in improving the performance of the alternating current light emitting diode (AC-LED). Finally, intense LEDs are successfully obtained by combining these phosphors with Ga(In)N near UV chips. PMID:29057839

Correlation of Structure, Tunable Colors, and Lifetimes of (Sr, Ca, BaAl2O4:Eu2+, Dy3+ Phosphors

Directory of Open Access Journals (Sweden)

Qidi Xie

2017-10-01

Full Text Available (Sr, Ca, BaAl2O4:Eu2+, Dy3+ phosphors were prepared via a high temperature solid-state reaction method. The correlation of phase structure, optical properties and lifetimes of the phosphors are investigated in this work. For the (Sr, CaAl2O4:Eu2+,Dy3+ phosphors, the different phase formation from monoclinic SrAl2O4 phase to hexagonal SrAl2O4 phase to monoclinic CaAl2O4 phase was observed when the Ca content increased. The emission color of SrAl2O4:Eu2+, Dy3+ phosphors varied from green to blue. For the (Sr, BaAl2O4:Eu2+, Dy3+ phosphors, different phase formation from the monoclinic SrAl2O4 phase to the hexagonal BaAl2O4 phase was observed, along with a shift of emission wavelength from 520 nm to 500 nm. More interestingly, the decay time of SrAl2O4:Eu2+, Dy3+changed due to the different phase formations. Lifetime can be dramatically shortened by the substitution of Sr2+ with Ba2+ cations, resulting in improving the performance of the alternating current light emitting diode (AC-LED. Finally, intense LEDs are successfully obtained by combining these phosphors with Ga(InN near UV chips.

Changes in sparkling wine aroma during the second fermentation under CO2 pressure in sealed bottle.

Science.gov (United States)

Martínez-García, Rafael; García-Martínez, Teresa; Puig-Pujol, Anna; Mauricio, Juan Carlos; Moreno, Juan

2017-12-15

High quality sparkling wine made by the traditional method requires a second alcoholic fermentation of a base wine in sealed bottles, followed by an aging time in contact with yeast lees. The CO 2 overpressure released during this second fermentation has an important effect on the yeast metabolism and therefore on the wine aroma composition. This study focuses on the changes in chemical composition and 43 aroma compounds released by yeast during this fermentation carried out under two pressure conditions. The data were subjected to statistical analysis allowing differentiating between the base wine and the wine samples taken in the middle and at the end of fermentation. The differentiation among wines obtained to the end of fermentation with or without CO 2 pressure is only achieved by a principal component analysis of 15 selected minor compounds (mainly ethyl dodecanoate, ethyl tetradecanoate, hexyl acetate, ethyl butanoate and ethyl isobutanoate). Copyright © 2017 Elsevier Ltd. All rights reserved.

Design, synthesis and luminescence properties of Ba2 YB2 O6 Cl- and Ba2 YB2 O6 F-based phosphors.

Science.gov (United States)

Chen, Wanping; Yang, Xin; Liu, Yan; Dai, Xiaoyan

2015-05-01

Using a high-temperature solid-state reaction, the chlorine in Ba2 YB2 O6 Cl is gradually replaced by F, and a new compound with the nominal chemical formula Ba2 YB2 O6 F and two phosphors doped with Ce(3+) and Eu(3+) , respectively, are obtained. X-Ray diffraction and photoluminescence spectroscopy are used to characterize the as-synthesized samples. The as-synthesized Ba2 YB2 O6 Cl exhibits bright blue emission in the spectral range ~ 330-410 nm with a maximum around 363 nm under X-ray or UV excitation. Ba2 YB2 O6 F:0.01Ce(3+) exhibits blue emission in the range ~ 340-570 nm with a maximum around 383 nm. Ba2 YB2 O6 F:0.01Eu(3+) exhibits a predominantly (5) D0 -(7)  F2 emission (~610 nm) and the relative intensities of the (5) D0 -(7)  F0,1,2 emissions are tunable under different wavelength UV excitation. The luminescence behaviors of the two phosphors are explained simply in terms of the host composition and site occupancy probability of Ce(3+) and Eu(3+) , respectively. The results indicate that these phosphors have potential application as a blue phosphor or as a red phosphor. Copyright © 2014 John Wiley & Sons, Ltd.

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

DEFF Research Database (Denmark)

Kjellström, Sven; Jensen, Ole Nørregaard

2004-01-01

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

Thermodynamic properties of 1-ethyl-4-nitro-1,2,3-triazole

Energy Technology Data Exchange (ETDEWEB)

Blokhin, Andrey V., E-mail: blokhin@bsu.by; Kohut, Sviataslau V.; Kabo, Gennady J.; Stepurko, Elena N.; Paulechka, Yauheni U.; Voitkevich, Olga V.

2013-08-10

Graphical abstract: - Highlights: • Heat capacities and phase transition enthalpies for 1-ethyl-4-nitro-1,2,3-triazole were measured. • Enthalpy of formation for 1-ethyl-4-nitro-1,2,3-triazole was determined. • Vapor pressure and enthalpy of sublimation of 1-ethyl-4-nitro-1,2,3-triazole were found from Knudsen measurements. - Abstract: Temperature dependence of the heat capacity and the parameters of phase transitions of 1-ethyl-4-nitro-1,2,3-triazole (1ET) were studied between 5 and 370 K in a vacuum adiabatic calorimeter. Thermodynamic properties of the 1ET in the condensed state were obtained over the range of 0–370 K. Saturated vapor pressure for crystalline 1ET in the temperature ranges from 313 to 344 K and its enthalpy of sublimation were measured by the Knudsen effusion method. The standard enthalpy of formation for crystalline 1ET at 298.15 K was determined in a static bomb combustion calorimeter. From these data, the standard enthalpy of formation for gaseous 1ET was evaluated. The enthalpy of formation calculated using quantum chemical methods is in excellent agreement with the experimental value.

Thermodynamic properties of 1-ethyl-4-nitro-1,2,3-triazole

International Nuclear Information System (INIS)

Blokhin, Andrey V.; Kohut, Sviataslau V.; Kabo, Gennady J.; Stepurko, Elena N.; Paulechka, Yauheni U.; Voitkevich, Olga V.

2013-01-01

Graphical abstract: - Highlights: • Heat capacities and phase transition enthalpies for 1-ethyl-4-nitro-1,2,3-triazole were measured. • Enthalpy of formation for 1-ethyl-4-nitro-1,2,3-triazole was determined. • Vapor pressure and enthalpy of sublimation of 1-ethyl-4-nitro-1,2,3-triazole were found from Knudsen measurements. - Abstract: Temperature dependence of the heat capacity and the parameters of phase transitions of 1-ethyl-4-nitro-1,2,3-triazole (1ET) were studied between 5 and 370 K in a vacuum adiabatic calorimeter. Thermodynamic properties of the 1ET in the condensed state were obtained over the range of 0–370 K. Saturated vapor pressure for crystalline 1ET in the temperature ranges from 313 to 344 K and its enthalpy of sublimation were measured by the Knudsen effusion method. The standard enthalpy of formation for crystalline 1ET at 298.15 K was determined in a static bomb combustion calorimeter. From these data, the standard enthalpy of formation for gaseous 1ET was evaluated. The enthalpy of formation calculated using quantum chemical methods is in excellent agreement with the experimental value

Synthesis of poly (3-hexyl thiophene-2,5-diyl) in presence of CdS nanoparticles: microscopic and spectroscopic studies

Energy Technology Data Exchange (ETDEWEB)

Nicho, M. E.; Jaimes, W. [Universidad Autonoma del Estado de Morelos, Centro de Investigacion en Ingenierias y Ciencias Aplicadas, Av. Universidad 1001, Col. Chamilpa, 62209 Cuernavaca, Morelos (Mexico); Rivas A, M. E.; Quevedo L, M. A. [University of Texas at Dallas, Department of Materials Science and Engineering, 800 West Campbell Road, Richardson, Texas 75252 (United States); Hu, H., E-mail: menicho@uaem.mx [UNAM, Instituto de Energias Renovables, 62580 Temixco, Morelos (Mexico)

2017-11-01

In this paper, the synthesis of nano composites of poly(3-hexyl thiophene-2,5-diyl) (P3HT) and cadmium sulfide (CdS) nanoparticles are reported. CdS nanoparticles were first synthesized using chemical precipitation. Then P3HT was synthesized by direct oxidation of 3-hexyl thiophene with FeCl{sub 3} as oxidant in presence of CdS nanoparticles. The goal of this work was to investigate the effect of the CdS nanoparticles during the synthesis of P3HT. The resulting films of P3HT/CdS nano composites were investigated by Fourier Transform Infrared Spectroscopy (Ft-IR), Ultraviolet-Visible Spectroscopy (UV-Vis), X-ray diffraction, Transmission electron microscopy (Tem), Atomic force microscopy (AFM) and Scanning electron microscopy (Sem). Homogeneous distribution of CdS nanoparticles in P3HT was demonstrated by Sem, AFM and Tem. Ft-IR analysis showed interaction between CdS and the S atoms of the thiophene rings. This result, together with UV-Vis spectra and XRD pattern suggest a better arrangement of the polymer chains. It is possible that the CdS nanoparticles are coupled with the unpaired electrons of S atoms in the thiophene rings through the positive delocalized charge, resulting in a more ordered P3HT polymer matrix with embedded CdS nanoparticles. (Author)

Notochord in Tilapia nilotica Exposed to Sublethal Dose of Malathion, S[1, 2-Di(EthoxycarbonylEthyl] Dimethyl Phosphorothiolothionate

Directory of Open Access Journals (Sweden)

Edna Amparado

1992-06-01

Full Text Available Exposure of Tilapia nilotica embryos to sublethal dose of 1.0 ppm commercial grade malathion, S[1,2-di(ethoxycarbonylethyl] dimethyl phosphorothiolothionate from day-10 post fertilization resulted in notochordal aberrations. Pesticide-treated fishes exhibited constriction of the notochordal sheath, folding at the posterior sections and larger notochord than those of the control group.

Photoluminescence properties of color-tunable SrMgAl10O17:Eu2+,Mn2+ phosphors for UV LEDs

International Nuclear Information System (INIS)

Ju Guifang; Hu Yihua; Chen Li; Wang Xiaojuan

2012-01-01

Aluminate phosphors SrMgAl 10 O 17 codoped with Eu 2+ and Mn 2+ ions were prepared by solid-state reaction. The phase structure and photoluminescence properties of the as-prepared phosphors were characterized by powder X-ray diffraction, photoluminescence excitation and emission spectra. Upon excitation of UV light, two broad emission bands centered at 470 and 515 nm were observed, and they were assigned to Eu 2+ and Mn 2+ emissions, respectively. The emission color of the phosphors can be tuned from blue to cyan and finally to green by adjusting the concentration ratios of Eu 2+ and Mn 2+ . Effective energy transfer occurs from Eu 2+ to Mn 2+ in the host due to the spectral overlap between the emission band of Eu 2+ and the excitation bands of Mn 2+ . The energy transfer mechanism was demonstrated to be electric dipole–quadrupole interaction. The energy transfer efficiency and critical distance were also calculated. The phosphors exhibit strong absorption in near UV spectral region and therefore they are potentially useful as UV-convertible phosphors for white LEDs. - Highlights: ► The strong absorption of phosphors matches well with the emission band of UV LED. ► The energy transfer from Eu 2+ to Mn 2+ in SrMgAl 10 O 17 was investigated in detail. ► The emission color can be tuned by adjusting the content of Eu 2+ and Mn 2+ . ► Two methods were employed to calculate the critical distance of energy transfer.

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.

Asymmetric criticality of ionic solution containing 1-hexyl-3-methylimidazolium tetrafluoroborate and 2-propanol

International Nuclear Information System (INIS)

Zhang, Xianshuo; Xu, Chen; Zheng, Peizhu; Yin, Tianxiang; Shen, Weiguo

2016-01-01

Highlights: • Liquid–liquid equilibrium of {2-propanol + RTIL} binary solution was measured. • The critical exponents were deduced and showed well agreements with 3D-Ising universality. • Asymmetry of the coexistence curve was analyzed by the complete scaling theory. • RPM-rescaled critical parameters were calculated. - Abstract: The liquid–liquid coexistence curve for binary solution {2-propanol + 1-hexyl-3-methylimidazolium tetrafluoroborate ([C_6mim][BF_4])} has been measured. The isobaric heat capacities per unit volume were obtained in both critical and non-critical regions. The critical exponents α and β were deduced and showed good agreement with those predicted for the 3D-Ising universality class. The asymmetric behaviour of the diameter of the coexistence curve was analysed based on the complete scaling theory, which indicated that the heat capacity related term plays an important role in describing the asymmetric behaviour of the coexistence curve. Furthermore, the RPM (restricted primitive model)-rescaled critical parameters were calculated and suggested the solvophobic criticality for this system.

Distribution of uranium in marine sediments; Distribucion de uranio en sedimentos marinos

Energy Technology Data Exchange (ETDEWEB)

Ordonez R, E.; Ramirez T, J.J.; Lopez M, J.; Aspiazu, J. [ININ, 52750 La Marquesa, Estado de Mexico (Mexico); Ruiz F, A.C. [U. Academica Mazatlan, ICML, UNAM (Mexico); Valero C, N. [CONALEP, 52000 Lerma, Estado de Mexico (Mexico)

2008-07-01

The marine sediments obtained by means of a sampling nucleus in the Gulf of Tehuantepec, Mexico, they have been object of crystallographic and morphological characterization. The PIXE analysis of some samples in study is shown. The normal methodology to carry out the alpha spectroscopy indicates that the sample should be dissolved, but due to the nature of the marine sediments, it thinks about the necessity to make a fractional separation of the sample components. In each stratum of the profile it separates the organic part and the mineral to recover the uranium. It was observed that in the organic phase, the uranium is in two oxidation states (IV and Vl), being necessary the radiochemical separation with a liquid/liquid column chromatographic that uses the di-2-ethyl hexyl phosphoric acid as stationary phase. The uranium compounds extracts are electrodeposited in fine layers on stainless steel disks to carry out the analysis by alpha spectroscopy. The spectroscopic analysis of the uranium indicates us that for each stratum one has a difference marked in the quotient of activities of {sup 234}U/{sup 238}U that depends on the nature of the studied fraction. These results give us a clear idea about how it is presented the effect of the uranium migration and other radioelements in the biosphere, with what we can determine which are the conditions in that these have their maximum mobility and to know their diffusion patterns in the different media studied. (Author)

Distribution of uranium in marine sediments

International Nuclear Information System (INIS)

Ordonez R, E.; Ramirez T, J.J.; Lopez M, J.; Aspiazu, J.; Ruiz F, A.C.; Valero C, N.

2008-01-01

The marine sediments obtained by means of a sampling nucleus in the Gulf of Tehuantepec, Mexico, they have been object of crystallographic and morphological characterization. The PIXE analysis of some samples in study is shown. The normal methodology to carry out the alpha spectroscopy indicates that the sample should be dissolved, but due to the nature of the marine sediments, it thinks about the necessity to make a fractional separation of the sample components. In each stratum of the profile it separates the organic part and the mineral to recover the uranium. It was observed that in the organic phase, the uranium is in two oxidation states (IV and Vl), being necessary the radiochemical separation with a liquid/liquid column chromatographic that uses the di-2-ethyl hexyl phosphoric acid as stationary phase. The uranium compounds extracts are electrodeposited in fine layers on stainless steel disks to carry out the analysis by alpha spectroscopy. The spectroscopic analysis of the uranium indicates us that for each stratum one has a difference marked in the quotient of activities of 234 U/ 238 U that depends on the nature of the studied fraction. These results give us a clear idea about how it is presented the effect of the uranium migration and other radioelements in the biosphere, with what we can determine which are the conditions in that these have their maximum mobility and to know their diffusion patterns in the different media studied. (Author)

Preparation of N(1-ethyl-2-pyrrolidyl-methyl)2-methoxy-4-iodo-125I-5-ethyl sulfonyl benzamide: a radioligand for the radioimmunoassay of sulpiride-related compounds

International Nuclear Information System (INIS)

Cardoso, M.T.; Pradelles, P.

1982-01-01

The preparation of 125 I labelling with a higher specific radioactivity of N(1-ethyl-2-pyrrolidyl-methyl)2-methoxy-5-ethyl sulfonyl benzamide, a potent biological analogue for sulpiride is described. The incorporation of iodine in the molecule was achieved by the substitution of aromatic amino groups via the diazo compound. Binding and immunological parameters of iodinated and tritiated tracers were compared. (author)

Sol-Gel Synthesis and Luminescence of Green Light Emitting Phosphors Zn2SiO4/Mn2+

Institute of Scientific and Technical Information of China (English)

无

2006-01-01

Mn2+ doped Zn2SiO4 phosphors were synthesized by sol-gel method, and the influence of zinc source, Mn2+ dopant concentration and annealing temperature were investigated. Results show that zinc nitrate based precursor with strong green emission intensities is better than zinc acetate based precursor. The intensity of green light emission reaches a peak at 254 nm when the Mn2+ dopant concentration is about 5%( molar percentage). Structural details of the phosphors were examined through X-ray diffractometry, thermogravimetric and differential thermal analysis. The result indicates that they are both rhombohedral structures, which remain amorphous below 700 ℃and crystallize completely around 1 000℃. The luminescent properties of Zn2SiO4/Mn2+ phosphors were characterized by excitation and emission spectra.

Photoluminescence properties of Eu2+-activated Ca2Y2Si2O9 phosphor

NARCIS (Netherlands)

Zhang, Zhijun; Delsing, A.C.A.; Notten, P.H.L.; Zhao, Jingtai; Hintzen, H.T.J.M.

2012-01-01

Eu2+-activated Ca2Y2Si2O9 phosphors with different Eu2+ concentrations have been prepared by a solid-state reaction method at high temperature and their photoluminescence (PL) properties were investigated. Photoluminescence results show that Eu2+-doped Ca2Y2Si2O9 can be efficiently excited by

Radiation crosslinking of highly plasticized PVC

Science.gov (United States)

Mendizabal, E.; Cruz, L.; Jasso, C. F.; Burillo, G.; Dakin, V. I.

1996-02-01

To improve the physical properties of highly plasticized PVC, the polymer was crosslinked by gamma irradiation using a dose rate of 91 kGy/h. The effect of plasticizer type was studied by using three different plasticizers, 2,2,4-trimethyl-1,3-pentanediol diisobutyrate (TXIB), di(2-ethyl hexyl) phthalate (DOP), and di(2-ethylhexyl terephthalate) (DOTP), and varying irradiation doses. Gel content was determined by soxhlet extraction, tensile measurements were made on a universal testing machine and the mechano-dynamic measurements were made in a dynamic rheometer. It was found that a considerable bonding of plasticizer molecules to macromolelcules takes place along with crosslinking, so that the use of the solvent extraction method for measuring the degree of crosslinking can give erroneous information. Radiation-chemical crosslinking yield ( Gc) and molecular weight of interjunctions chains ( Mc), were calculated for different systems studied. Addition of ethylene glycol dimethacrylate (EGDM) as a crosslinking coagent and dioctyl tin oxide (DOTO) as a stabilizer was also studied. Plasticizers extraction resistance was increased by irradiation treatment.

Radiation crosslinking of highly plasticized PVC

International Nuclear Information System (INIS)

Mendizabal, E.; Cruz, L.; Jasso, C.F.; Burillo, G.; Dakin, V.I.

1996-01-01

To improve the physical properties of highly plasticized PVC, the polymer was crosslinked by gamma irradiation using a dose rate of 91 kGy/h. The effect of plasticizer type was studied by using three different plasticizers, 2,2,4-trimethyl-1,3-pentanediol diisobutyrate (TXIB), di(2-ethyl hexyl) phthalate (DOP), and di(2-ethylhexyl terephthalate) (DOTP), and varying irradiation doses. Gel content was determined by soxhlet extraction, tensile measurements were made on a universal testing machine and the mechano-dynamic measurements were made in a dynamic rheometer. It was found that a considerable bonding of plasticizer molecules to macromolecules takes place along with crosslinking, so that the use of the solvent extraction method for measuring the degree of crosslinking can give erroneous information. Radiation-chemical crosslinking yield (G c ) and molecular weight of interjunctions chains (M c ), were calculated for different systems studied. Addition of ethylene glycol dimethyacrylate (EGDM) as a crosslinking coagent and dioctyl tin oxide (DOTO) as a stabilizer was also studied. Plasticizers extraction resistance was increased by irradiation treatment. (author)

Synthesis, structure, and luminescence properties of SrSiAl2O3N2:Eu(2+) phosphors for light-emitting devices and field emission displays.

Science.gov (United States)

Wang, Xicheng; Zhao, Zhengyan; Wu, Quansheng; Li, Yanyan; Wang, Chuang; Mao, Aijun; Wang, Yuhua

2015-06-28

A series of SrSiAl2O3N2:Eu(2+) (0.005 ≤x≤ 0.05) phosphors were successfully synthesized through a pressureless, facile, and efficient solid state route. The crystal structure, band structure, and their photoluminescence and cathodoluminescence properties were investigated in detail. The phosphors exhibit rod shape morphology with a uniform Eu(2+) distribution. Under n-UV excitation the emission spectra shift from 477 to 497 nm with an increase of Eu(2+) concentration. The concentration quenching mechanism of Eu(2+) emission was dominated by the dipole-dipole interaction. The thermal stability is comparable to that of the commercial Ba2SiO4:Eu(2+) phosphor. The phosphor also exhibits high current saturation and high resistance under low voltage electron bombardment. All the results indicate that the SrSiAl2O3N2:Eu(2+) phosphors can be considered as candidates for application in both white LEDs and FEDs.

Preparation of Methacrylate End-functionalized Poly(2-ethyl-2-oxazoline) Macromonomers

NARCIS (Netherlands)

Weber, C.; Becer, C.R.; Baumgaertel, A.; Hoogenboom, R.; Schubert, U.S.

2009-01-01

Three methods for the functionalization of 2-ethyl-2-oxazoline (EtOx) oligomers with a methacrylate or methacrylamide unit are compared to identify the best suitable route to obtain such macromolecules. In the first method, a functional initiator, namely methacryloyl chloride, was used for the

Spectroscopic properties of Eu{sup 3+}:KLa(WO{sub 4}){sub 2} novel red phosphors

Energy Technology Data Exchange (ETDEWEB)

Rasu, K. Kavi; Balaji, D.; Babu, S. Moorthy, E-mail: babusm@yahoo.com

2016-02-15

Eu{sup 3+}:KLa(WO{sub 4}){sub 2} (Eu:KLW) phosphors were prepared through Pechini type sol–gel method. Low temperature synthesis was achieved through polyesterification between citric acid and ethylene glycol during the growth procedure. The properties of phosphors were analysed using X-ray diffractogram (XRD), scanning electron microscopy (SEM), Raman and luminescence spectroscopy. An effective energy transfer from the tungstate matrix to the activator Eu{sup 3+} was observed. Intense red emission in Eu:KLW phosphors was observed while excited with f–f transitions of Eu{sup 3+}. The Judd–Ofelt (J–O) intensity parameters Ω{sub 2} and Ω{sub 4} were obtained from the emission intensities of {sup 5}D{sub 0}→{sup 7}F{sub 2},{sub 4,} respectively by taking the magnetic dipole {sup 5}D{sub 0}→{sup 7}F{sub 1} emission band intensity as reference. The CIE colour co-ordinates of the Eu:KLW red phosphors was calculated (x=0.650, y=0.348), which are close to NTSC standard values. - Highlights: • Eu:KLW phosphors were synthesized by pechini type sol–gel method. • Structural, morphological, vibrational and luminescence properties were well investigation. • Eu{sup 3+}:KLa(WO{sub 4}){sub 2} phosphors has strong red emission at about 615 nm ({sup 5}D{sub 0}→{sup 7}F{sub 2}) under the excitation of near UV and blue LEDs regions. • Decay measurement and Judd–Ofelt parameter were calculated and dicussed. • These phosphors can serve as a potential candidate for red source for White LEDs application.

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

Indian Academy of Sciences (India)

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

Current extraction and separation of uranium, thorium and rare earths elements from monazite leach solution using organophosphorous extractants

International Nuclear Information System (INIS)

Biswas, Sujoy; Rupawate, V.H.; Hareendran, K.N.; Roy, S.B.

2014-01-01

A new process based on solvent extraction has been developed for separation of uranium, thorium and rare earths from monazite leach solution using organophosphorous extractants. The Thorium cake coming from monazite source was dissolved in HNO 3 medium in presence of trace amount of HF for feed preparation. The separation of U(VI) was carried out by liquid-liquid extraction using tris-2-ethyl hexyl phosphoric acid (TEHP) in dodecane leaving thorium and rare earths elements in the raffinate. The thorium from raffinate was selectively extracted using 1M tri iso amyl phosphate (TiAP) in dodecane in organic phase leaving all rare earths elements in aqueous solution. The uranium and thorium from organic medium was quantitatively stripped using 0.05 M HNO 3 counter current mode. Results indicate the quantitative separation of uranium, thorium and rare earths from thorium cake (monazite source) using organophosphorous extractant in counter current mode

SYNTHESIS OF ENANTIOMERICALLY PURE (R)-2-SULFANYLPROPANOIC AND (S)-2-SULFANYLPROPANOIC ACIDS (THIOLACTIC ACID) FROM ETHYL (S)-LACTATE USING PIG-LIVER ESTERASE

NARCIS (Netherlands)

HOF, RP; KELLOGG, RM

1995-01-01

The methanesulfonates of optically pure ethyl (S)-lactate or ethyl (R)-2-chloropropanoate 5, obtained with inversion of configuration from ethyl (S)-lactate on treatment with SOCl2, can be substituted by caesium thiolates with inversion of configuration to yield (R) and (S) ethyl

Crystal structure, thermally stability and photoluminescence properties of novel Sr10(PO4)6O:Eu2+ phosphors

International Nuclear Information System (INIS)

Guo, Qingfeng; Liao, Libing; Mei, Lefu; Liu, Haikun

2015-01-01

A series of novel luminescent phosphors Sr 10 (PO 4 ) 6 O:Eu 2+ with apatite structure were synthesized via a high temperature solid-state reaction. The phase structure, photoluminescence (PL) properties, the PL thermal stability, as well as the fluorescence decay curves of the samples were investigated to characterize the resulting samples, and the selected Sr 9.97 (PO 4 ) 6 O:0.03Eu 2+ phosphor exhibits strong thermal quenching resistance, retaining the luminance of 88.73% at 150 °C. The quenching concentration of Eu 2+ in Sr 10 (PO 4 ) 6 O was about 0.03 attributing to the dipole–quadrupole interaction. The Sr 10 (PO 4 ) 6 O:Eu 2+ phosphor exhibited a broad-band blue emission at 439 nm upon excitation at 346 nm. The results indicate that Sr 10 (PO 4 ) 6 O:Eu 2+ phosphors have potential applications as near UV-convertible phosphors for white-light UV LEDs. - Graphical abstract: Sr 10 (PO 4 ) 6 O:Eu 2+ phosphors have potential applications as near UV-convertible phosphors for white-light UV LEDs. - Highlights: • Sr 9.97 (PO 4 ) 6 O:0.03Eu 2+ phosphor exhibits strong thermal quenching resistance. • Two different Eu 2+ emission centers exists in Sr 10 (PO 4 ) 6 O. • The activation energy was also estimated for the Eu 2+ luminescence center

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

Recent progress in fission product separation

International Nuclear Information System (INIS)

Raggenbass, A.

1964-01-01

Successful experiments have been done on the method described at Geneva in 1958. The process has been considerably improved: 1 - Initially, the caesium phospho tungstate precipitate was leached barium hydroxide in the centrifuge and this was followed by a distillation of ammonia in a concentrator. The barium hydroxide was then eliminated by carbonate precipitation and centrifugation. It has been proved that the ammonia distillation could be replaced by its evaporation during centrifugation, thus eliminating the need of a concentrator. It was then possible to carry out the carbonation on the solide-liquid mixture produced by the baryte water leaching. 2 - In applying the above process to the treatment of solutions derived from uranium molybdenum fuels, concentrating is to be recommended in order to hold the molybdenum in solution by complexing it with phosphoric acid. This complexing process provides a suspension of zirconium phosphate and ammonium phospho tungstate. These are separated by passing into a basic medium which precipitates the zirconium oxide, then turning back to an acid medium; the end of the treatment remains unchanged. 3 - Studies carried out in several countries on the exchange properties of hetero-polyacid salts have always met with difficulties as a result of the poor mechanical properties of these substances. This difficulty has been overcome by wrapping the ammonium phospho tungstate in a zirconium phosphate matrix. The exchanger obtained possesses: satisfactory mechanical properties, - a capacity of 0.1 milli equivalent per gram in concentrated nitric acid solution. It can be eluted and regenerated by a solution of an ammonium salt. The procedure for recovery of these various fission products is briefly the following: extraction of rare earths by di-2-ethyl hexyl phosphoric acid into dodecane at pH 2, the chemical impurities being complexed by citric acid, extraction of most of the magnesium at pH 4 by the same solvents the solvent being

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

Eu and Sr2CeO4 : Eu phosphors suitable for near ultraviolet excitation

Indian Academy of Sciences (India)

Administrator

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

Green-emissive transparent BaSi 2O 5:Eu 2 + film phosphor on quartz glass created by a sputtering thermal diffusion process

Science.gov (United States)

Seo, K. I.; Park, J. H.; Kim, J. S.; Na, Y. H.; Choi, J. C.; Bae, J. S.

2009-10-01

Eu 2+-doped BaSi 2O 5 film phosphors on quartz substrates are fabricated by radio-frequency magnetron sputtering thermal diffusion. The BaSi 2O 5: Eu 2+ phosphor crystals have some preferred orientations that are lattice-spacing matched with the crystallized β- SiO 2 crystals, and they show pore and grain boundary-free morphology with a rod-like shape fused into the crystallized β- SiO 2 crystals. The BaSi 2O 5: Eu 2+ film phosphor has a high transparency, with a transmittance of about 30% in visible light. The BaSi 2O 5: Eu 2+ film phosphor shows 510 nm green emission from the f-d transition of the Eu 2+ ions, and in particular the best sample shows a green photoluminescence brightness of about 5% of a BaSi 2O 5: Eu 2+ powder phosphor screen. These excellences in optical properties can be explained by less optical scattering at pores or grain boundaries, and less reflection at the continuously index-changed interface.

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

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

Directory of Open Access Journals (Sweden)

Yan Shirun

2017-12-01

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

(Zn, Mg)2GeO4:Mn2+ submicrorods as promising green phosphors for field emission displays: hydrothermal synthesis and luminescence properties.

Science.gov (United States)

Shang, Mengmeng; Li, Guogang; Yang, Dongmei; Kang, Xiaojiao; Peng, Chong; Cheng, Ziyong; Lin, Jun

2011-10-07

(Zn(1-x-y)Mg(y))(2)GeO(4): xMn(2+) (y = 0-0.30; x = 0-0.035) phosphors with uniform submicrorod morphology were synthesized through a facile hydrothermal process. X-Ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), photoluminescence (PL), and cathodoluminescence (CL) spectroscopy were utilized to characterize the samples. SEM and TEM images indicate that Zn(2)GeO(4):Mn(2+) samples consist of submicrorods with lengths around 1-2 μm and diameters around 200-250 nm, respectively. The possible formation mechanism for Zn(2)GeO(4) submicrorods has been presented. PL and CL spectroscopic characterizations show that pure Zn(2)GeO(4) sample shows a blue emission due to defects, while Zn(2)GeO(4):Mn(2+) phosphors exhibit a green emission corresponding to the characteristic transition of Mn(2+) ((4)T(1)→(6)A(1)) under the excitation of UV and low-voltage electron beam. Compared with Zn(2)GeO(4):Mn(2+) sample prepared by solid-state reaction, Zn(2)GeO(4):Mn(2+) phosphors obtained by hydrothermal process followed by high temperature annealing show better luminescence properties. In addition, codoping Mg(2+) ions into the lattice to substitute for Zn(2+) ions can enhance both the PL and CL intensity of Zn(2)GeO(4):Mn(2+) phosphors. Furthermore, Zn(2)GeO(4):Mn(2+) phosphors exhibit more saturated green emission than the commercial FEDs phosphor ZnO:Zn, and it is expected that these phosphors are promising for application in field-emission displays.

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

Energy Technology Data Exchange (ETDEWEB)

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

2016-07-15

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

Emission Studies in CI Engine using LPG and Palm Kernel Methyl Ester as Fuels and Di-ethyl Ether as an Additive

Science.gov (United States)

Dora, Nagaraju; Jothi, T. J. Sarvoththama

2018-05-01

The present study investigates the effectiveness of using di-ethyl ether (DEE) as the fuel additive in engine performance and emissions. Experiments are carried out in a single cylinder four stroke diesel engine at constant speed. Two different fuels namely liquefied petroleum gas (LPG) and palm kernel methyl ester (PKME) are used as primary fuels with DEE as the fuel additive. LPG flow rates of 0.6 and 0.8 kg/h are considered, and flow rate of DEE is varied to maintain the constant engine speed. In case of PKME fuel, it is blended with diesel in the latter to the former ratio of 80:20, and DEE is varied in the volumetric proportion of 1 and 2%. Results indicate that for the engine operating in LPG-DEE mode at 0.6 kg/h of LPG, the brake thermal efficiency is lowered by 26%; however, NOx is subsequently reduced by around 30% compared to the engine running with only diesel fuel at 70% load. Similarly, results of PKME blended fuel showed a drastic reduction in the NOx and CO emissions. In these two modes of operation, DEE is observed to be significant fuel additive regarding emissions reduction.

Blue–green afterglow of BaAl{sub 2}O{sub 4}:Dy{sup 3+} phosphors

Energy Technology Data Exchange (ETDEWEB)

Zhai, Bao-gai [School of Mathematics and Physics, Changzhou University, Jiangsu 213164 (China); Ma, Qing-lan [School of Mathematics and Physics, Changzhou University, Jiangsu 213164 (China); School of Electronics and Information, Nantong University, Jiangsu 226019 (China); Xiong, Rui [School of Physics and Technology, Wuhan University, Hubei 430072 (China); Li, Xiazhang [Analysis and Testing Center, Changzhou University, Jiangsu 213164 (China); Huang, Yuan Ming, E-mail: dongshanisland@126.com [School of Mathematics and Physics, Changzhou University, Jiangsu 213164 (China)

2016-03-15

Highlights: • Afterglow can be achieved when Eu{sup 2+} is absent in the DyAl{sub 2}O{sub 4}:Dy{sup 3+} phosphors. • The afterglow of DyAl{sub 2}O{sub 4}:Dy{sup 3+} phosphors is discernible to naked eyes for minutes. • Dy{sup 3+} introduced trap centers are believed to be responsible for the afterglow. - Abstract: Dy{sup 3+} doped barium aluminate (BaAl{sub 2}O{sub 4}:Dy{sup 3+}) phosphors were prepared via the sol–gel combustion route at the ignition temperature of 600 °C. The phosphors were characterized with X-ray diffractometry, scanning electron microscopy, transmission electron microscopy, photoluminescence spectroscopy, Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy. Regardless of the absence of Eu{sup 2+} luminescent centers, broadband blue–green afterglow with its peak at about 490 nm was recorded in the BaAl{sub 2}O{sub 4}:Dy{sup 3+} phosphors. The decay profile of the blue–green afterglow can be best fitted into a two-component exponential function with the two lifetime decay constants to be 8.81 and 45.25 s, respectively. The observation of blue–green afterglow from BaAl{sub 2}O{sub 4}:Dy{sup 3+} in the absence of Eu{sup 2+} provides unique opportunity in unveiling the afterglow mechanisms of rare-earth doped alkaline-metal aluminates. Possible mechanisms on the blue–green afterglow in BaAl{sub 2}O{sub 4}:Dy{sup 3+} phosphors are discussed in terms of the Dy{sup 3+} ions introduced trap centers as well as luminescent centers in the crystal lattice.

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

Science.gov (United States)

Verma, Tarkeshwari; Agrawal, Sadhana

2018-01-01

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

Concentration quenching of Eu{sup 2+} in a thermal-stable yellow phosphor Ca{sub 2}BO{sub 3}Cl:Eu{sup 2+} for LED application

Energy Technology Data Exchange (ETDEWEB)

Zhang Xinguo; Zhang Jilin; Dong Zhiyue; Shi Jianxin [State Key Laboratory of Optoelectronic Materials and Technologies, Ministry of Education Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275 (China); Gong Menglian, E-mail: cesgml@mail.sysu.edu.cn [State Key Laboratory of Optoelectronic Materials and Technologies, Ministry of Education Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-sen University, Guangzhou 510275 (China)

2012-04-15

A piece-shaped phosphor Ca{sub 2}BO{sub 3}Cl: Eu{sup 2+} was synthesized by solid-state reaction method. This phosphor exhibited wide absorption in ultra-violet and visible range, and bright yellow emission band centering at 570 nm. The concentration quenching mechanism was verified to be a dipole-dipole interaction, and its critical transfer distance was about 17 A by both calculated crystal structural method and experimental spectral method. This phosphor has a good thermal stability with a quenching temperature (T{sub 1/2}) of 200 Degree-Sign C. Yellow and white LEDs were fabricated with this phosphor and near UV chips, and the yellow LED has a high color purity of 97.0% and promising current tolerant property, while the white LED shows a luminous efficiency of 11.68 lm/W. - Highlights: Black-Right-Pointing-Pointer Broadband excitable and strong yellow-emitting Ca{sub 2}BO{sub 3}Cl: Eu{sup 2+} phosphor is obtained by solid state reaction. Black-Right-Pointing-Pointer Concentration quenching mechanism of Ca{sub 2}BO{sub 3}Cl: Eu{sup 2+} is dipole-dipole interaction. Black-Right-Pointing-Pointer Quenching temperature (T{sub 1/2}) of Ca{sub 2}BO{sub 3}Cl: Eu{sup 2+} is at 200 Degree-Sign C. Black-Right-Pointing-Pointer As synthesized material can be used for LED phosphor application.

Di-4-octylphenylphosphoric acid as extractant : extraction of vanadium (IV) and beryllium

International Nuclear Information System (INIS)

Gajankush, R.B.

1976-01-01

The extraction of vanadium and beryllium has been studied using di-4-octylphenyl phosphoric acid (DOPPA) as metal extractant. The factors which affect the extraction have been studied in detail. An attempt has been made to clarify the mechanism of extraction and compare the results with those reported for di-2-ethylhexyl phosphoric acid (DEHPA). In the case of vanadium it was found that vanadium (IV) is more suitable for extraction. Synergistic extractionwas observed in the presence of neutral organophosphorous compounds like tri-n-butyl phosphate (TBP), dibutyl butyl phosphate (DBBP) and tri-n-octyl phosphine oxide (TOPO). The possibility of separating vanadium and uranium when they are present together in leach solutions has also been studied. The extraction of beryllium was found to be a slow process. The factors controlling the rate as well as the extent of extraction have been investigated. However, the results showed that in both respects DOPPA is better than DEHPA which was earlier studied by other authors. The separation of aluminium from beryllium has also been studied. (author)

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.

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

Super-bright and short-lived photoluminescence of textured Zn2SiO4:Mn2+ phosphor film on quartz glass

Science.gov (United States)

Park, Jehong; Park, Kwangwon; Lee, Jaebum; Kim, Jongsu; Seo, Kwangil; Kwon, Kevin; Kung, Patrick; Kim, Seongsin M.

2010-02-01

Green-emissive textured Zn2SiO4:Mn2+ phosphor film was fabricated by a thermal diffusion of ZnO:Mn on quartz glass. The characterization has been performed in terms of Mn2+ ions concentration (Mn/Zn=1~9 mol %). As an increase of Mn2+ ions concentration in the Zn2SiO4:Mn2+ phosphor film, the emission peak was red shifted from 519 nm to 526 nm, and the decay time to 10% of the maximum intensity was shorter from 20 ms to 0.5 ms. All annealed Zn2SiO4:Mn2+ phosphor films became textured along some hexagonal directions on the amorphous quartz glass. The brightest Zn2SiO4:Mn2+ film at optimal Mn2+ concentration of 5 % showed the photoluminescence brightness of 65 % and the shortened decay time of 4.4 ms in comparison with a commercially Zn2SiO4: Mn2+ powder phosphor screen. The excellencies can be attributed to a unique textured structure.

Persistent luminescence and thermoluminescence of UV/VIS -irradiated SrAl2O4: Eu2+, Dy3+ phosphor

International Nuclear Information System (INIS)

Pereyda-Pierre, C.; Meléndrez, R.; García, R.; Pedroza-Montero, M.; Barboza-Flores, M.

2011-01-01

The persistent luminescence and thermoluminescence properties of SrAl 2 O 4 : Eu 2+ , Dy 3+ phosphors excited with UV–VIS light in the 200–500 nm region were investigated. The thermoluminescence glow curve was found to be composed of peaks around 70, 125 and 245 °C. The persistent luminescence and thermoluminescence excitation spectra exhibited a broad band around 300–500 nm centered at 400 and 420 nm respectively. A linear behavior of the integrated thermoluminescence intensity and persistent luminescence versus irradiation time was found for the first 60 s. The charge detrapping from the 70 °C trapping levels was the major contributor to the observed persistent luminescence at room temperature. The SrAl 2 O 4 : Eu 2+ , Dy 3+ phosphors have suitable properties to be applied as storage and persistent luminescence UV–VIS irradiation dose phosphor. -- Highlights: ► SrAl 2 O 4 :Eu 2+ , Dy 3+ persistent luminescence and thermoluminescence was measured. ► The phosphor was irradiated with UV–VIS photons in the 200–500 nm wavelength range. ► SrAl 2 O 4 :Eu 2+ , Dy 3+ behaves adequately as persistent and storage UV–VIS dosimeter. ► The persistent luminescence dosimetry does not require heat or light stimulation.

Investigation on photoluminescence, electrical and positron lifetime of Eu"3"+ activated Gd_2O_3 phosphors

International Nuclear Information System (INIS)

Selvalakshmi, Thangaraj; Sellaiyan, Selvakumar; Uedono, Akira; Chandra Bose, Arumugam

2015-01-01

In the present study, red emitting Gd_2O_3:Eu"3"+ phosphors are prepared by citrate-based sol–gel process and the as-prepared samples are annealed at various annealing temperatures. The photoluminescence properties of Gd_2O_3:Eu"3"+ is explained from the excitation and emission spectra. The excitation spectra include peaks corresponding to charge transfer and 4f–4f transitions of Eu"3"+ and Gd"3"+. The phosphors exhibit a weak energy transfer process from Gd"3"+ to Eu"3"+. Under the excitation of 254 nm, a sharp red emission peak is observed at 611 nm and the emission intensity increases with the annealing temperature. The presence of defects in the phosphor is investigated by positron annihilation lifetime and Doppler broadening spectroscopy. The relation between visible emission and lattice defects of the phosphors is presented. The electrical and dielectric properties of the phosphor are also discussed in detail. Such red emitting phosphors pave the way towards the fabrication of light emitting diodes (LEDs). - Highlights: • Positron annihilation lifetime spectroscopy of Gd_2O_3:Eu"3"+. • Relation between positron lifetime and photoluminescence. • Conductivity and dielectric properties of Gd_2O_3:Eu"3"+.

Preparation and photoluminescence properties of Mn2+-activated M2Si5N8 (M = Ca, Sr, Ba) phosphors

NARCIS (Netherlands)

Duan, C.J.; Otten, W.M.; Delsing, A.C.A.; Hintzen, H.T.J.M.

2008-01-01

Mn2+-doped M2Si5N8 (M=Ca, Sr, Ba) phosphors have been prepared by a solid-state reaction method at high temperature and their photoluminescence properties were investigated. The Mn2+-activated M2Si5N8 phosphors exhibit narrow emission bands in the wavelength range of 500–700 nm with peak center at

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

[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.

Novel green-emitting Na2CaPO4F:Eu2+ phosphors for near-ultraviolet white light-emitting diodes

International Nuclear Information System (INIS)

Huang, Chien-Hao; Chen, Yen-Chi; Kuo, Te-Wen; Chen, Teng-Ming

2011-01-01

In this study, green-emitting Na 2 CaPO 4 F:Eu 2+ phosphors were synthesized by solid-state reactions. The excitation spectra of the phosphors showed a broad hump between 250 and 450 nm; the spectra match well with the near-ultraviolet (NUV) emission spectra of light-emitting diodes (LEDs). The emission spectrum showed an intense broad emission band centered at 506 nm. White LEDs were fabricated by integrating a 390 nm NUV chip comprising blue-emitting BaMgAl 10 O 17 :Eu 2+ , green-emitting Na 2 CaPO 4 F:0.02 Eu 2+ , and red-emitting CaAlSiN 3 :Eu 2+ phosphors into a single package; the white LEDs exhibited white light with a correlated color temperature of 5540 K, a color-rendering index of 90.75, and color coordinates (0.332, 0.365) close to those of ideal white light. - Highlights: → Novel green-emitting Na 2 CaPO 4 F:Eu 2+ phosphors were synthesized by solid-state reactions in this research. → White LEDs were fabricated by integrating a 390 nm NUV chip comprising blue-emitting BaMgAl 10 O 17 :Eu 2+ , green-emitting Na 2 CaPO 4 F:0.02Eu 2+ , and red-emitting CaAlSiN 3 :Eu 2+ phosphors into a single package. → The white LEDs exhibited white light with a correlated color temperature of 5540 K, a color-rendering index of 90.75, and color coordinates (0.332, 0.365) close to those of ideal white light.

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.

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.

Synthesis and in vivo evaluation of [O-methyl-11C](2R,4R)-4-hydroxy-2-[2-[2-[2-(3-methoxy)phenyl]ethyl]phenoxy] ethyl-1-methylpyrrolidine as a 5-HT2A receptor PET ligand

International Nuclear Information System (INIS)

Kumar, J.S. Dileep; Prabhakaran, Jaya; Erlandsson, Kjell; Majo, Vattoly J.; Simpson, Norman R.; Pratap, Mali; Heertum, Ronald L. van; Mann, J. John; Parsey, Ramin V.

2006-01-01

The serotonin 2A (5-HT 2A ) receptor is implicated in the pathophysiology of schizophrenia and mood disorders, and in vivo studies of this receptor would be of value in studying the pathophysiology of these disorders and in measuring the relationship of clinical response to receptor occupancy for 5-HT 2A antagonists such as atypical antipsychotics. Therefore, (2R,4R)-4-hydroxy-2-[2-[2-[2-(3-methoxy)-phenyl]ethyl] phenoxy]ethyl-1-methylpyrrolidine (MPM) (13), a selective and high-affinity (K i =0.79 nM) 5HT 2A antagonist, has been radiolabeled with carbon-11 by O-methylation of the corresponding desmethyl analogue (2R,4R)-4-hydroxy-2-[2-[2-[2-(3-hydroxy)phenyl]ethyl]phenoxy] ethyl-1-methylpyrrolidine (12) with [ 11 C]methyltriflate in order to determine the suitability of [ 11 C]MPM to quantify 5-HT 2A in living brain using PET. Desmethyl-MPM 12 and standard MPM were prepared, starting from 3-hydroxymethylphenol (2), in excellent yield. The yield obtained for radiolabeling was 40±5% (EOB), and the total synthesis time was 30 min at EOS. PET studies with [ 11 C]MPM in baboon showed a distribution in the brain consistent with the known distribution of 5-HT 2A receptors. The time-activity curves for the high-binding regions peaked at ∼45 min after injection. Blocking studies with M100907 demonstrated not only 38-57% blocking of tracer binding in brain regions known to have 5-HT 2A receptors but also 38% blocking in cerebellum, which has a low 5-HT 2A receptor concentration. Although [ 11 C]MPM exhibits appropriate kinetics in baboon for imaging 5-HT 2A receptors, its specific binding in cerebellum and higher proportion of nonspecific binding limit its usefulness for the in vivo quantification of 5-HT 2A receptors with PET

Improved photoluminescence properties of a new green SrB2O4:Tb3+ phosphor by charge compensation

International Nuclear Information System (INIS)

Wu, Zhan-Chao; Wang, Ping; Liu, Jie; Li, Chao; Zhou, Wen-Hui; Kuang, Shao-Ping

2012-01-01

Highlights: ► New green-emitting SrB 2 O 4 :Tb 3+ phosphor was synthesized by solid-state reaction. ► Li + , Na + , and K + can all increase luminescent intensity of SrB 2 O 4 :Tb 3+ . ► Na + is the optimal charge compensator among Li + , Na + and K + . ► SrB 2 O 4 :Tb 3+ is a promising green phosphor for fabricating WLED. -- Abstract: A new green-emitting SrB 2 O 4 :Tb 3+ phosphor was synthesized by solid-state reaction. X-ray powder diffraction (XRD) analysis confirmed all the samples with orthorhombic formation of SrB 2 O 4 . The excitation spectra indicate the phosphor can be effectively excited by near ultraviolet (NUV) light, making it attractive as conversion phosphor for LED applications. The phosphor exhibits a bright green emission with the highest photoluminescence (PL) intensity at 544 nm excited by 378 nm light. The critical quenching concentration of Tb 3+ in SrB 2 O 4 :Tb 3+ is about 10 mol%. The effects of charge compensators (Li + , Na + , and K + ) on photoluminescence of SrB 2 O 4 :Tb 3+ were also studied. The results show that the emission intensity can be improved by all the three charge compensators and Na + is the optimal one for SrB 2 O 4 :Tb 3+ . All properties show that the phosphor is a promising green phosphor pumped by NUV InGaN chip for fabricating white light-emitting diodes (WLEDs).

Luminescent properties of red-emitting LiSr4B3O(9−3x/2)Nx:Eu2+ phosphor for white-LEDs

International Nuclear Information System (INIS)

Yu Hua; Deng Degang; Xu Shiqing; Yu Cuiping; Yin Haoyong; Nie Qiulin

2012-01-01

An Eu 2+ -activated oxynitride LiSr (4−y) B 3 O (9−3x/2) N x :yEu 2+ red-emitting phosphor was synthesized by solid-state reactions. The synthesized phosphor crystallized in a cubic system with space group Ia–3d. The LiSr 4 B 3 O (9−3x/2) N x :Eu 2+ phosphors exhibited a broad red emission band with a peak at 610 nm and a full width at half maximum of 106 nm under 410 nm excitation, which is ascribed to the 4f 6 5d 1 →4f 7 transition of Eu 2+ . The optimal doped nitrogen concentration was observed to be x=0.75. The average decay times of two different emission centers were estimated to be 568 and 489 ns in the LiSr 3.99 B 3 O 8.25 N 0.5 :0.01Eu 2+ phosphors, respectively. Concentration quenching of Eu 2+ ions occurred at y=0.07, and the critical distance was determined as 17.86 Å. The non-radiative transitions via dipole–dipole interactions resulted in the concentration quenching of Eu 2+ -site emission centers in the LiSr 4 B 3 O 9 host. These results indicate LiSr 4 B 3 O (9−3x/2) N x :Eu 2+ phosphor is promising for application in white near-UV LEDs. - Highlights: ► An oxynitride LiSr 4 B 3 O 9 N:Eu 2+ red-emitting phosphor was prepared at low synthesis temperature. ► The introduced nitrogen improved the excitation and emission intensity of the phosphor. ► The wide excitation band matches well with near-UV LED chips. ► The emission spectrum of the phosphor showed a broad full width at half maximum of about 106 nm.

Evaluation of Gd{sub 2}O{sub 2}S:Pr granular phosphor properties for X-ray mammography imaging

Energy Technology Data Exchange (ETDEWEB)

David, S.; Michail, C. [Department of Biomedical Engineering, Technological Educational Institute (TEI) of Athens, Ag. Spyridonos Street, 122 10 Egaleo (Greece); Seferis, I. [Department of Biomedical Engineering, Technological Educational Institute (TEI) of Athens, Ag. Spyridonos Street, 122 10 Egaleo (Greece); Faculty of Chemistry, Wroclaw University, 14F Joliot-Curie Street, 50-383 Wroclaw (Poland); Valais, I.; Fountos, G.; Liaparinos, P.; Kandarakis, I. [Department of Biomedical Engineering, Technological Educational Institute (TEI) of Athens, Ag. Spyridonos Street, 122 10 Egaleo (Greece); Kalyvas, N., E-mail: nkalyvas@teiath.gr [Department of Biomedical Engineering, Technological Educational Institute (TEI) of Athens, Ag. Spyridonos Street, 122 10 Egaleo (Greece)

2016-01-15

Phosphor materials are widely used in X-ray medical imaging detector applications, coupled with suitable photoreceptors. Upon the most demanding imaging modality is X-ray mammography, since the best defense against breast cancer is its early detection. A material suitable as a mammographic detector should efficiently absorb X-ray photons and transform them to optical photons, so as to minimize breast dose. The aim of the present study was to investigate the X-ray absorption efficiency and the absolute efficiency (AE), defined as the output optical photon power divided by the incident exposure, of Gd{sub 2}O{sub 2}S:Pr powder scintillator. For the purposes of this study, three scintillating screens with coating thicknesses, 34.1, 46.0 and 81.5 mg/cm{sup 2} respectively, were prepared in our laboratory from Gd{sub 2}O{sub 2}S:Pr powder (Phosphor Technology, Ltd.) by sedimentation on silica substrates. The quantum detection efficiency (QDE), the energy absorption efficiency (EAE), the spectral matching factor and the absolute efficiency (AE) were evaluated for X-ray mammographic conditions. Furthermore theoretical models were utilized to investigate the optical photon transmission properties through the phosphor mass. Gd{sub 2}O{sub 2}S:Pr presented high X-ray absorption properties and good spectral compatibility with several photoreceptors. It may be utilized for X-ray mammographic imaging if it is put in conjunction with a sensitive photoreceptor, so as to enhance Gd{sub 2}O{sub 2}S:Pr light emission properties. - Highlights: • Gd{sub 2}O{sub 2}S:Pr phosphor evaluated for mammography detectors. • The X-ray absorption efficiency was found high. • Spectral matching compatibility found for several photoreceptors. • X-ray absolute efficiency measured smaller than other phosphors. • Optical diffusion length and the light transmission per layer was theoretically calculated.

Gamma radiation induced sensitization and photo-transfer in Mg2SiO4:Tb TLD phosphor

International Nuclear Information System (INIS)

Lakshmanan, A.R.; Vohra, K.G.

1979-01-01

Mg 2 SiO 4 :Tb TLD phosphor was found to show enhanced TL sensitivity to both gamma and UV radiations after high pre-gamma exposures (>100 R) and a post-annealing treatment at 300 0 C for 1 h. Maximum sensitization factors of 2.8 and 55 were obtained at the pre-expsoure levels of 5.2x10 1 C/kg and 1.3x10 3 C/kg for gamma and UV test radiations respectively. The near constancy of the intensity of the residual TL (RTL) peak at 500 0 C for the sensitized sample with increasing test-gamma exposures has ruled out the re-trapping model proposed earlier for the gamma radiation induced sensitization in this phosphor. The Tsub(max) for the sensitized phosphor was found to occur at a higher temperature compared to that for the virgin phosphor. The dependence of sensitization on RTL was explained qualitatively on the basis of competition between sensitization traps (having higher energy than the dosimetry traps) and RTL traps while capturing the charge carriers generated during the test-gamma exposure. The sensitization observed in this phosphor to UV test radiation was found to be a consequence of the photo-transfer of charge carriers from deep (RTL) traps to the shallow (dosimetry) traps. The reduction in RTL peak (500 0 C) intensity of the sensitized sample with increasing test-UV exposure has demonstrated the photo-transfer mechanism in this phosphor. The TL response of the virgin Mg 2 SiO 4 :Tb phosphor was found to be supralinear to both gamma and UV radiations. The TL response of the sensitized phosphor was found to be linear to gamma radiation and sublinear to UV radiation. (Auth.)

Crystal structure of 1,3-bis(4-hexyl-5-iodothiophen-2-yl-4,5,6,7-tetrahydro-2-benzothiophene

Directory of Open Access Journals (Sweden)

Julian Linshoeft

2014-10-01

Full Text Available In the crystal structure of the title compound, C28H36I2S3, a terthiophene monomer, the central thiophene unit is arranged anti-coplanar to the two outer thiophene rings. There are two crystallographically independent molecules in the asymmetric unit, which show different conformations. In one molecule, the dihedral angles between the inner and the two outer thiophene rings are 15.7 (3 and 3.47 (3°, whereas these values are 4.2 (3 and 11.3 (3° for the second molecule. Differences are also found in the arrangement of the hexyl chains: in one of the two molecules, both chains are nearly in plane to the central moiety, whereas in the second molecule, only one chain is in plane and the other one is nearly perpendicular to the central moiety. Some of the C atoms are disordered and were refined using a split model with occupancy ratios of 0.65:0.35 and 0.70:0.30 in the two molecules.

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

International Nuclear Information System (INIS)

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

2016-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2014-02-15

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

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

Science.gov (United States)

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

2016-04-13

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

Studies on Three Liquid Phase Extraction (TLPE) system for separation of rare earths

International Nuclear Information System (INIS)

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

2014-01-01

Three-liquid-phase extraction (TLPE) is relatively a new separation technique, which takes the advantage of the differences in physicochemical properties of three coexisted phases to achieve multi-phase liquid separation of two or more components in one-step extraction. TLPE system consists of three liquid layers namely an organic solvent phase (organophosphorous type) and two aqueous phases one rich in polymer phase (poly alkylene glycol) and other a salt solution. To study the feasibility of using such system for separation of rare earths, it is important to optimize the preparatory conditions by selective suitable polymer and salt solutions at an appropriate pH to obtain a stable three phase layers to effect the separation. D2EHPA (di-2-ethyl hexyl phosphoric acid) is a well- established extractant in the rare earth industry and has been chosen in the present work to form a TLPE with polymer and salt solution. In the present investigation after preparing the stable three phase, the feasibility of using TLPE has been examined to separate rare earths from a multicomponent solutions. This study has demonstrated the ability of TLPE having D2EHPA as organic phase to separate rare earths from a multicomponent system. Effect of pH, concentration and types of polymer, complexing agent and D2EHPA concentration has been studied. Variation in pH study indicated that 4.0 leads to extraction of rare earths in the polymer phase. PEG 600 was found to be best amongst the polymer investigated. Presence of DTPA as complexing agent in the salt solution having pH >4.0 resulted in enhanced extraction of rare earths in PEG phase

Defect mediated optical properties in ZnAl2O4 phosphor

Science.gov (United States)

Pathak, Nimai; Saxena, Suryansh; Kadam, R. M.

2018-04-01

The present work describes defect mediated optical properties in ZnAl2O4 phosphor material, synthesized through sol-gel combustion method, which has potential to be used both as a blue emitting phosphor material as well as white emitting, depending upon the annealing temperature during the synthesis procedure. Various defect centers such as anionic vacancy, cationic vacancy, antisite defects etc. create different electronic states inside the band gap, which are responsible for the multicolour emission. The interesting colour tunable emission characteristics can be linked with the various defect centers and their changes upon annealing.

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

International Nuclear Information System (INIS)

Yang Hongmei; Shi Jianxin; Liang Hongbin; Gong Menglian

2006-01-01

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

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

International Nuclear Information System (INIS)

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

2015-01-01

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

Ca2 Al2 SiO7 :Ce3+ phosphors for mechanoluminescence dosimetry.

Science.gov (United States)

Tiwari, Geetanjali; Brahme, Nameeta; Sharma, Ravi; Bisen, D P; Sao, Sanjay Kumar; Sahu, Ishwar Prasad

2016-12-01

A series of Ce 3+ ion single-doped Ca 2 Al 2 SiO 7 phosphors was synthesized by a combustion-assisted method at an initiating temperature of 600 °C. The samples were annealed at 1100 °C for 3 h and their X-ray diffraction patterns confirmed a tetragonal structure. The phase structure, particle size, surface morphology and elemental analysis were analyzed using X-ray diffraction (XRD), transmission electron microscope (TEM), scanning electron microscopy (SEM) and energy dispersive X-ray (EDX) spectroscopy techniques. Thermoluminescence (TL) intensity increased with increase in ultraviolet (UV) light exposure time up to 15 min. With further increase in the UV irradiation time the TL intensity decreases. The increase in TL intensity indicates that trap concentration increased with UV exposure time. A broad peak at 121 °C suggested the existence of a trapping level. The peak of mechanoluminescence (ML) intensity versus time curve increased linearly with increasing impact velocity of the moving piston. Mechanoluminescence intensity increased with increase in UV irradiation time up to 15 min. Under UV-irradiation excitation, the TL and ML emission spectra of Ca 2 Al 2 SiO 7 :Ce 3+ phosphor showed the characteristic emission of Ce 3+ peaking at 400 nm (UV-violet) and originating from the Ce 3+ transitions of 5d-4f ( 2 F 5/2 and 2 F 7/2 ). The photoluminescence (PL) emission spectra for Ca 2 Al 2 SiO 7 :Ce 3+ were similar to the ML/TL emission spectra. The mechanism of ML excitation and the suitability of the Ca 2 Al 2 SiO 7 :Ce 3+ phosphor for radiation dosimetry are discussed. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

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)

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

International Nuclear Information System (INIS)

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

1996-02-01

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

Effect of UV irradiation on different types of luminescence of SrAl2 O4 :Eu,Dy phosphors.

Science.gov (United States)

Jha, Piyush

2016-11-01

This paper reports the luminescence behavior of Sr 0.097 Al 2 O 4 :Eu 0.01 ,Dy 0.02 phosphors under UV-irradiation. The effect of UV-irradiation on afterglow (AG), thermoluminescence (TL) and mechanoluminescence (ML) of Sr 0.097 Al 2 O 4 :Eu 0.01 ,Dy 0.02 phosphors is investigated. The space group of Sr 0.097 Al 2 O 4 :Eu 0.01 ,Dy 0.02 phosphors is monoclinic P2 1 . The prepared phosphors exhibit a long AG, intense TL and ML. It is found that the AG, ML intensity and TL increase with increasing duration of irradiation time. The ML intensity decreases with successive impact of the load onto the phosphors, whereby the diminished ML intensity can be recovered by UV-irradiation. Copyright © 2016 John Wiley & Sons, Ltd. Copyright © 2016 John Wiley & Sons, Ltd.

UV absorption coefficients of Y2(1-x-y)Gd2xEu2yO3 phosphors

International Nuclear Information System (INIS)

Ling, M.; Yocom, P.W.; Soules, T.F.

1990-01-01

The ability of a phosphor to absorb 254 nm excitation is important in the development of phosphors for fluorescent lamps. Recently the optical properties of phosphor coating were modeled using ray tracing Monte-Carlo techniques. These calculations provided a relationship between absorptance measured on a semi-infinite plaque at a given wavelength and the product of the absorption coefficient of the phosphor and its particle diameter. The purpose of this work is to provide experimental data for comparison with the calculated data, to demonstrate a technique for obtaining absorption coefficients and to provide UV absorption coefficients obtained in this way for important yttrium oxide europium red-emitting phosphors

Phase equilibrium measurements and thermodynamic modelling for the system (CO2 + ethyl palmitate + ethanol) at high pressures

International Nuclear Information System (INIS)

Gaschi, Priscilla S.; Mafra, Marcos R.; Ndiaye, Papa M.; Corazza, Marcos L.

2013-01-01

Graphical abstract: Ethyl palmitate and biodiesel comparison in a pressure–composition diagram for the systems (CO 2 + ethyl palmitate + biodiesel), at different temperatures. Highlights: ► We measured VLE, LLE, and VLLE for the system (CO 2 + ethyl palmitate + ethanol). ► The saturation pressures were obtained using a variable-volume view cell. ► Phase envelope of (CO 2 + ethyl palmitate) is different that (CO 2 + soybean oil biodiesel). ► The experimental data were modeled using PR-vdW2 and PR–WS equations of state. - Abstract: This work reports phase equilibrium measurements for the binary {CO 2 (1) + ethyl palmitate(2)} and ternary {CO 2 (1) + ethyl palmitate(2) + ethanol(3)} systems at high pressures. There is currently great interest in biodiesel production processes involving supercritical and/or pressurized solvents, such as non-catalytic supercritical biodiesel production and enzyme-catalysed biodiesel production. Also, supercritical CO 2 can offer an interesting alternative for glycerol separation in the biodiesel purification step in a water-free process. In this context, the main goal of this work was to investigate the phase behaviour of binary and ternary systems involving CO 2 , a pure constituent of biodiesel ethyl palmitate and ethanol. Experiments were carried out in a high-pressure variable-volume view cell with operating temperatures ranging from (303.15 to 353.15) K and pressures up to 21 MPa. The CO 2 mole fraction ranged from 0.5033 to 0.9913 for the binary {CO 2 (1) + ethyl palmitate(2)} system and from 0.4436 to 0.9712 for ternary system {CO 2 (1) + ethyl palmitate(2) + ethanol(3)} system with ethyl ester to ethanol molar ratios of (1:6), (1:3), and (1:1). For the systems investigated, vapour–liquid (VL), liquid–liquid (LL) and vapour–liquid–liquid (VLL) phase transitions were observed. The experimental data sets were successfully modeled using the Peng–Robinson equation of state with the classical van der Waals

Studies on up-gradation of Erbium from a heavy fraction of rare earths with EHEHPA

International Nuclear Information System (INIS)

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

2014-01-01

Erbium is an important heavy rare earth element, which finds wide applications. Recently, use of Erbium oxide as structural coating material in fusion reactor has stimulated the interest in obtaining Erbium in pure form. The separation of Erbium from other rare earths such as Dy, Ho, Y, Yb, Tm etc is very difficult due to low separation factor owing to their similar chemical properties. Additionally due to very low concentration ( 2 O 3 : 1.09, Dy 2 O 3 : 58.07, Er 2 O 3 : 22.0, Ho 2 O 3 : 13.33, Yb 2 O 3 : 4.74, Tm 2 O 3 :0.67 is obtained during purification of Y by Aliquat 336 from thiocyanate medium. In the present investigation this HRE fraction is taken as the feed material for up-gradation of Er by an acidic extractant namely 2 ethyl hexyl - 2 ethyl hexyl phosphonic acid (EHEHPA)

Titanium di-oxide films using a less hygroscopic colloidal precursor

Energy Technology Data Exchange (ETDEWEB)

Vandana,, E-mail: vandana1@nplindia.org; Batra, Neha; Kumar, Praveen; Sharma, Pooja; Singh, P.K., E-mail: pksingh@nplindia.org

2014-04-01

We report the study of titanium dioxide films (TiO{sub 2}) using titanium di-isopropoxyl di-2ethyl hexanoate Ti(OC{sub 3}H{sub 7}){sub 2} (C{sub 7}H{sub 15}COO){sub 2} colloidal precursor. This compound is less hygroscopic in nature and easy to use with processes like spin or dip coating. Thin films of TiO{sub 2} are made on silicon substrates and their structural and optical properties are studied. The effect of Ti content in the precursor, sintering temperature and its duration on film thickness and refractive index are investigated. Refractive index shows an increasing trend with the rise in the sintering temperature but remains unchanged with the time. The film thickness decreases with both sintering temperature and time and increases with Ti content in the precursor. Reflectivity measurements show marked reduction in the reflection losses compared to bare silicon surface wherein the film thickness is altered by spin speed. XRD results show anatase phase in the samples sintered at lower temperature (<680 °C), however, a mix of anatase, brookite and rutile phases is seen above this temperature. In the samples sintered above 1100 °C, rutile phase is dominant. These results are supported by the X-ray photoelectron spectroscopy. Atomic force microscopy reveals larger grain size at higher sintering temperature. The titanium dioxide films of desirable thickness and refractive index could be used as an antireflection coating on solar cells. - Highlights: • TiO{sub 2} films are made using titanium di-isopropoxyl di-2ethyl hexanoate precursor. • Effect of Ti content in the precursor, sintering temperature and time is studied. • Refractive index (μ) increases with sintering temperature but is independent of time. • Films of desired thickness and μ could be used as an antireflection coating. • XRD results show that rutile phase dominates in samples sintered above 1100 °C.

Dielectric study of molecular association in the binary mixtures (2-ethyl-1-hexanol + alcohol) and (cyclohexane + alcohol) at 298.2 K

Energy Technology Data Exchange (ETDEWEB)

Ghanadzadeh, A. [Department of Chemistry, Guilan University, Rasht (Iran, Islamic Republic of)]. E-mail: aggilani@guilan.ac.ir; Ghanadzadeh, H. [Department of Chemical Engineering, Guilan University, Rasht (Iran, Islamic Republic of); Sariri, R. [Department of Chemistry, Guilan University, Rasht (Iran, Islamic Republic of); Ebrahimi, L. [Department of Chemistry, Guilan University, Rasht (Iran, Islamic Republic of)

2005-04-15

Experimental results of dielectric investigations of three binary mixtures (ethanol + 2-ethyl-1-hexanol), (n-butanol + 2-ethyl-1-hexanol), and (tert-butanol + 2-ethyl-1-hexanol) were reported for various mole fractions at 298.2 K. The variations of dipole moment and correlation factor, g, with mole fraction in these mixtures were investigated using a unified quasichemical method described by Durov. The molecular associations of (ethanol + cyclohexane), (n-butanol + cyclohexane), and (tert-butanol + cyclohexane) binary mixtures were also investigated using the static dielectric method. A similar trend was observed in the variation of the dipole moments with the solute mole fractions in the both binary systems (i.e., alcohol + 2-ethyl-1-hexanol and alcohol + cyclohexane)

Photocatalytic Ethanol Oxidative Dehydrogenation over Pt/TiO2: Effect of the Addition of Blue Phosphors

Directory of Open Access Journals (Sweden)

J. J. Murcia

2012-01-01

Full Text Available Ethanol oxidative dehydrogenation over Pt/TiO2 photocatalyst, in the presence and absence of blue phosphors, was performed. The catalyst was prepared by photodeposition of Pt on sulphated TiO2. This material was tested in a gas-solid photocatalytic fluidized bed reactor at high illumination efficiency. The effect of the addition of blue phosphors into the fluidized bed has been evaluated. The synthesized catalysts were extensively characterized by different techniques. Pt/TiO2 with a loading of 0.5 wt% of Pt appeared to be an active photocatalyst in the selective partial oxidation of ethanol to acetaldehyde improving its activity and selectivity compared to pure TiO2. In the same way, a notable enhancement of ethanol conversion in the presence of the blue phosphors has been obtained. The blue phosphors produced an increase in the level of ethanol conversion over the Pt/TiO2 catalyst, keeping at the same time the high selectivity to acetaldehyde.

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2010-12-01

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

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.

Synthesis and Structure Determination of Di-tert-butyltin (IV) Dithiocarbamate)

International Nuclear Information System (INIS)

Amirah Faizah Abdul Muthalib; Ibrahim Baba; Yang Farina Abdul Aziz; Mohd Wahid Samsudin

2013-01-01

New diorganotin (IV) dithiocarbamate complexes have been synthesized from di-tert-butyltin (IV) dichloride, N-dialkylamine and carbon disulphide. Elemental and gravimetric analysis confirmed the general formula of these complexes as (t- C 4 H 9 ) 2 Sn[S 2 CNR 1 R 2 ] 2 (R 1 = CH 3 , C 2 H 5 , C 7 H 7 dan R 2 = C 2 H 5 , C 6 H 11 , iC 3 H 7 , CH 3 , C 2 H 5 , C 4 H 9 , C 7 H 7 ). The structures of these complexes have been elucidated on the basis of infrared, ultraviolet, 1 H, 13 C and 119 Sn NMR spectroscopy and X-ray crystallography. The infrared spectra of these complexes showed three main peaks for v(C-N), v(C-S) and v(Sn-S) bands that appeared in the region of 1447-1496, 947-988 and 352-370 cm -1 , respectively. The 13 C NMR spectrum showed the chemical shift for ?(N 13 CS 2 ) in the range of 199.1-201.8 ppm. X-ray single crystal structure (C 4 H 9 ) 2 Sn[S 2 CN(CH 3 )(iC 3 H 7 )] 2 demonstrated a six-coordination geometry around the tin atom adopting a monoclinic system with a space group of P2/n with a = 11.2934(11) Angstrom, b = 7.0175(7) Angstrom, c = 15.6894(15) Angstrom; β = 95.016(1) degree. The (N-benzyl-N-ethyl dithiocarbamato)chloride di-tert-butyltin(IV) and (N,N-dibenzyl dithiocarbamato)chloride-di-(tert-butyl)tin(IV) formed a different geometry with one dithiocarbamate ligand and one chlorine atom attached to the tin centre to form a five-coordinate structure. Crystal of (N-benzyl-N-ethyl dithiocarbamato)chloride di-tert-butyltin(IV) adopts a triclinic system with space group of P1 and cell parameter of a = 8.6140 (2) Angstrom, b = 10.9604 (3) Angstrom, c = 11.4765 (3) Angstrom; α = 91.858 (2) degree, β = 96.193 (2) degree, γ = 96.011 (2) degree, while (N,N-dibenzyl dithiocarbamato)chloride-di-(tert-butyl)tin(IV) adopts a monoclinic system with space group of P2 i with cell parameter a = 9.0600 (2) Angstrom, b = 10.9238 (2) Angstrom, c = 12.7845 (3) Angstrom; β= 102.759 (2) degree. (author)

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.

Evaluation Lactogenic Activity of Ethyl Acetate Fraction of Torbangun (Coleus amboinicus L.) Leaves

Science.gov (United States)

Damanik, R. M.; Kustiyah, L.; Hanafi, M.; Iwansyah, A. C.

2017-12-01

This study aimed to assess the lactogenic property of ethyl acetate fraction of torbangun (Coleus amboinicus L.) leaves and to identify the compounds that responsibility as ‘milk booster’ using LC- MS approach. Lactagogue activity was evaluated in terms of quantity of milk produced from the rats treated with commercial milk booster (AF), ethyl acetate fraction of torbangun leaves (EA), water extraction of torbangun (AQ) and kaempferol (KP). The feed was given orally every two days and starting from Day 2 after giving birth until Day 28. The performance of milk production was measured along the experimental period by weight-suckle-weight method. The level of prolactin serum was determined by ELISA methods. Histopathological analysis of mammary gland, liver, intestines and kidney tissues was carried out. Moreover, in order to profiling and identification of compounds of ethyl acetate fraction, ultra-performance liquid chromatography quadrupole time of flight to electrospray ionization mass spectrometry (UPLC-QTOF-ESI-MS) in the positive-ion mode was performed. The ethyl acetate fraction of torbangun leaves (EA) was induced milk production about 17%, and AF 22% and KP 51% compared to the control group. Meanwhile, the EA was not significantly stimulate the synthesis of serum prolactin at Day 14 and Day 28 (p>0.05). Administration of EA did not cause any signs or symptoms of toxicity. In addition, a total of ten compounds was identified by UPLC-QTOF-ESI/MS in the ethyl acetate fraction of the leaves of C. amboinicus, mostly phenolic compounds, flavonols and some of their glycoside derivatives, such as: digiprolatone, and kaempferol-3-7-O-di-rhamnopyranoside. The present study reveals the ethyl acetate fraction of torbangun leaves and its bioactive compounds has the potency as a remedy for stimulating and improving milk production.

3-Chloro-2-ethyl-6-nitro-2H-indazole

Directory of Open Access Journals (Sweden)

Mohamed Mokhtar Mohamed Abdelahi

2017-05-01

Full Text Available In the title compound, C9H8ClN3O2, the orientation of the ethyl substituent is partly determined by an intramolecular C—H...Cl hydrogen bond. The indazole moiety is slightly folded with an angle of 0.70 (8° between the five- and six-membered rings. In the crystal, molecules pack in layers parallel to [100] through C—H...π(ring and N...;O...π(ring interactions.

Correlation of Structure, Tunable Colors, and Lifetimes of (Sr, Ca, Ba)Al₂O₄:Eu2+, Dy3+ Phosphors.

Science.gov (United States)

Xie, Qidi; Li, Bowen; He, Xin; Zhang, Mei; Chen, Yan; Zeng, Qingguang

2017-10-18

(Sr, Ca, Ba)Al₂O₄:Eu 2+ , Dy 3+ phosphors were prepared via a high temperature solid-state reaction method. The correlation of phase structure, optical properties and lifetimes of the phosphors are investigated in this work. For the (Sr, Ca)Al₂O₄:Eu 2+ ,Dy 3+ phosphors, the different phase formation from monoclinic SrAl₂O₄ phase to hexagonal SrAl₂O₄ phase to monoclinic CaAl₂O₄ phase was observed when the Ca content increased. The emission color of SrAl₂O₄:Eu 2+ , Dy 3+ phosphors varied from green to blue. For the (Sr, Ba)Al₂O₄:Eu 2+ , Dy 3+ phosphors, different phase formation from the monoclinic SrAl₂O₄ phase to the hexagonal BaAl₂O₄ phase was observed, along with a shift of emission wavelength from 520 nm to 500 nm. More interestingly, the decay time of SrAl₂O₄:Eu 2+ , Dy 3+ changed due to the different phase formations. Lifetime can be dramatically shortened by the substitution of Sr 2+ with Ba 2+ cations, resulting in improving the performance of the alternating current light emitting diode (AC-LED). Finally, intense LEDs are successfully obtained by combining these phosphors with Ga(In)N near UV chips.

Photoluminescence and phosphorescence properties of Sr1-xZn2-y(PO4)2:Eux2+,Mny2+ phosphor for UV-based white-LEDs

International Nuclear Information System (INIS)

Jeong, Junho; Jayasimhadri, M.; Sueb Lee, Ho; Jang, Kiwan; Soo Yi, Soung; Hyun Jeong, Jung; Kim, Changdae

2009-01-01

Sr 1-x Zn 2-y (PO 4 ) 2 :Eu x 2+ ,Mn y 2+ (SZP: Eu x 2+ ,Mn y 2+ ) phosphors (x=0, 0.01 and y=0, 0.01) were prepared by using a stoichiometric solid-state reaction method and their photoluminescence and phosphorescence decay properties were investigated. The emission spectrum of SrZn 2 (PO 4 ) 2 :Eu 0.01 2+ , Mn 0.01 2+ measured under 400 nm excitation was composed of the violettish blue and the emerald green emissioins centered at 421 and 547 nm, respectively. The excitation wavelength of the emission peak at 547 nm was about 421 nm in the excitation spectrum of SZP:Mn 0.01 2+ . Since, this value is equal to the transition energy of Eu 2+ , the energy transfer from Eu 2+ to Mn 2+ in SZP:Eu 0.01 2+ ,Mn 0.01 2+ phosphor has been demonstrated. The CIE chromaticity coordinates of SZP:Eu 0.01 2+ ,Mn 0.01 2+ phosphor were (0.330, 0.328) under the excitation wavelength 375 nm at room temperature. The phosphorescence from SZP:Eu 0.01 2+ ,Mn 0.01 2+ could be seen by naked eyes for few seconds and it has persisted for about 4.4 h while monitoring by using a PMT spectrometer. Therefore, SZP:Eu x 2+ ,Mn y 2+ phosphor may be a potential candidate for the UV-based white light-emitting diodes (LEDs).

Icosapent ethyl for the treatment of severe hypertriglyceridemia

Directory of Open Access Journals (Sweden)

Fares H

2014-06-01

Full Text Available Hassan Fares,1 Carl J Lavie,2,3 James J DiNicolantonio,4 James H O'Keefe,5 Richard V Milani2 1Department of Hospital Medicine, Ochsner Medical Center, New Orleans, LA, 2Department of Cardiovascular Diseases, John Ochsner Heart and Vascular Institute, Ochsner Clinical School, University of Queensland School of Medicine, New Orleans, LA, 3Department of Preventive Medicine, Pennington Biomedical Research Center, Louisiana State University System, Baton Rouge, LA, 4Mid America Heart Institute at Saint Luke's Hospital, Kansas City, MO, 5Mid America Heart Institute, University of Missouri–Kansas City, Kansas City, MO, USA Abstract: Hypertriglyceridemia is a highly prevalent lipid abnormality and it is associated with atherosclerosis, with a growing body of evidence linking elevated triglycerides (TGs with cardiovascular disease. The current major omega-3 polyunsaturated fatty acids, eicosapentaenoic acid (EPA/docosahexaenoic acid (DHA combination, lowers serum TGs while often increasing levels of low-density lipoprotein cholesterol. Icosapent ethyl is an omega-3 polyunsaturated fatty acid with a 96% pure ethyl ester of EPA that has been recently approved for lowering TG levels in patients with very high TGs (≥500 mg/dL, and it does so without significantly affecting serum low-density lipoprotein cholesterol. The potential benefits of omega-3 fatty acid therapy for dyslipidemias will be discussed, including the potential pros and cons of EPA alone versus the more common and readily available EPA/DHA combination therapy. Keywords: triglycerides, low-density lipoprotein, eicosapentaenoic acid, docosahexaenoic acid

High efficiency nitride based phosphores for white LEDs

NARCIS (Netherlands)

Li, Yuan Qiang; Hintzen, H.T.J.M.

2008-01-01

In this overview paper, novel rare-earth doped silicon nitride based phosphors for white LEDs applications have been demonstrated. The luminescence properties of orange-red-emitting phosphors (M2Si5N8:Eu2+) and green-to-yellow emitting phosphors (MSi2N2O2:Eu2+, M = Ca, Sr, Ba) are discussed in

An orange emitting phosphor Lu2−xCaMg2Si2.9Ti0.1O12:xCe with pure garnet phase for warm white LEDs

International Nuclear Information System (INIS)

Chu, Yaoqing; Zhang, Qinghong; Xu, Jiayue; Li, Yaogang; Wang, Hongzhi

2015-01-01

A new silicate garnet phosphor, Lu 2−x CaMg 2 Si 2.9 Ti 0.1 O 12 :xCe was synthesized by a high temperature solid-state reaction under reductive atmosphere. X-ray diffraction (XRD) showed that the powder was pure garnet phase. The emission and excitation spectrum indicated that the Lu 2−x CaMg 2 Si 2.9 Ti 0.1 O 12 :xCe phosphors could absorb blue light in the spectral range of 400–550 nm efficiently and exhibit bright yellow–orange emission in the range of 520–750 nm. With the increase of Ce 3+ concentration, the emission band of Ce 3+ showed a red shift. Interestingly, the concentration quenching occurred when the Ce 3+ concentration exceeded 4 mol%. The temperature-dependent luminescent properties of the phosphors were discussed and the Lu 1.96 CaMg 2 Si 2.9 Ti 0.1 O 12 :0.04Ce phosphors showed good performances in color temperature (2430 K) and potential applications for warm white LEDs. - Graphical Abstract: This image shows that the phosphor of Lu 1.96 CaMg 2 Si 2.9 Ti 0.1 O 12 :0.04Ce can generate a uniform yellow tint under natural light illumination and emit orange–red light when excited by blue light. With a fixed 467 nm emission light, warm white light can be produced by this phosphor, which indicates that the phosphor is potentially applicable in warm white light emitting diodes based on GaN chips. - Highlights: • A new silicate garnet phosphor was synthesized by solid-state method. • Secondary phases can be avoided when a small amount of Si 4+ were replaced by Ti 4+ . • A broad emission band of Ce 3+ in the phosphors was described. • The phosphors are potentially applicable in warm white light emitting diodes

Excellent Brightness with Shortening Lifetime of Textured Zn2SiO4:Mn2+ Phosphor Films on Quartz Glass

Science.gov (United States)

Park, Jehong; Park, Kwangwon; Lee, Jaebum; Kim, Jongsu; Kim, Seongsin Margaret; Kung, Patrick

2010-04-01

Green-emissive textured Zn2SiO4:Mn2+ phosphor films were fabricated by the thermal diffusion of ZnO:Mn on quartz glass. The Zn2SiO4:Mn2+ phosphor films became textured along several hexagonal directions and their chemical composition was continuously graded at the interface. The decay time of Mn2+ was as short as 4.4 ms, and the optical transition probability of the films defined as the inverse of decay time showed a strong correlation with film texture degree as a function of annealing temperature. The brightest Zn2SiO4:Mn2+ film showed a photoluminescent brightness as high as 65% compared with a commercial Zn2SiO4:Mn2+ phosphor powder screen and a maximum absolute transparency of 70%. These excellent optical properties are explained by the combination of the unique textured structure and continuous grading of the Zn2SiO4:Mn2+ chemical composition at the interface.

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

International Nuclear Information System (INIS)

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

2011-01-01

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

Synthesis and in vivo evaluation of [O-methyl-{sup 11}C](2R,4R)-4-hydroxy-2-[2-[2-[2-(3-methoxy)phenyl]ethyl]phenoxy] ethyl-1-methylpyrrolidine as a 5-HT{sub 2A} receptor PET ligand

Energy Technology Data Exchange (ETDEWEB)

Kumar, J.S. Dileep [Dept. of Psychiatry, College of Physicians and Surgeons, Columbia University, New York, NY 10032 (United States)]|[Div. of Brain Imaging, Dept. of Neuroscience, New York State Psychiatric Institute, New York, NY 10032 (United States)]. E-mail: dk2038@columbia.edu; Prabhakaran, Jaya [Dept. of Psychiatry, College of Physicians and Surgeons, Columbia University, New York, NY 10032 (United States); Erlandsson, Kjell [Dept. of Psychiatry, College of Physicians and Surgeons, Columbia University, New York, NY 10032 (United States)]|[Dept. of Radiology, College of Physicians and Surgeons, Columbia University, New York, NY 10032 (United States); Majo, Vattoly J. [Dept. of Psychiatry, College of Physicians and Surgeons, Columbia University, New York, NY 10032 (United States); Simpson, Norman R. [Dept. of Radiology, College of Physicians and Surgeons, Columbia University, New York, NY 10032 (United States); Pratap, Mali [Dept. of Psychiatry, College of Physicians and Surgeons, Columbia University, New York, NY 10032 (United States)]|[Div. of Brain Imaging, Dept. of Neuroscience, New York State Psychiatric Institute, New York, NY 10032 (United States); Heertum, Ronald L. van [Dept. of Radiology, College of Physicians and Surgeons, Columbia University, New York, NY 10032 (United States); Mann, J. John [Dept. of Psychiatry, College of Physicians and Surgeons, Columbia University, New York, NY 10032 (United States)]|[Dept. of Radiology, College of Physicians and Surgeons, Columbia University, New York, NY 10032 (United States)]|[Div. of Brain Imaging, Dept. of Neuroscience, New York State Psychiatric Institute, New York, NY 10032 (United States); Parsey, Ramin V. [Dept. of Psychiatry, College of Physicians and Surgeons, Columbia University, New York, NY 10032 (United States)]|[Div. of Brain Imaging, Dept. of Neuroscience, New York State Psychiatric Institute, New York, NY 10032 (United States)

2006-05-15

The serotonin{sub 2A} (5-HT{sub 2A}) receptor is implicated in the pathophysiology of schizophrenia and mood disorders, and in vivo studies of this receptor would be of value in studying the pathophysiology of these disorders and in measuring the relationship of clinical response to receptor occupancy for 5-HT{sub 2A} antagonists such as atypical antipsychotics. Therefore, (2R,4R)-4-hydroxy-2-[2-[2-[2-(3-methoxy)-phenyl]ethyl] phenoxy]ethyl-1-methylpyrrolidine (MPM) (13), a selective and high-affinity (K {sub i}=0.79 nM) 5HT{sub 2A} antagonist, has been radiolabeled with carbon-11 by O-methylation of the corresponding desmethyl analogue (2R,4R)-4-hydroxy-2-[2-[2-[2-(3-hydroxy)phenyl]ethyl]phenoxy] ethyl-1-methylpyrrolidine (12) with [{sup 11}C]methyltriflate in order to determine the suitability of [{sup 11}C]MPM to quantify 5-HT{sub 2A} in living brain using PET. Desmethyl-MPM 12 and standard MPM were prepared, starting from 3-hydroxymethylphenol (2), in excellent yield. The yield obtained for radiolabeling was 40{+-}5% (EOB), and the total synthesis time was 30 min at EOS. PET studies with [{sup 11}C]MPM in baboon showed a distribution in the brain consistent with the known distribution of 5-HT{sub 2A} receptors. The time-activity curves for the high-binding regions peaked at {approx}45 min after injection. Blocking studies with M100907 demonstrated not only 38-57% blocking of tracer binding in brain regions known to have 5-HT{sub 2A} receptors but also 38% blocking in cerebellum, which has a low 5-HT{sub 2A} receptor concentration. Although [{sup 11}C]MPM exhibits appropriate kinetics in baboon for imaging 5-HT{sub 2A} receptors, its specific binding in cerebellum and higher proportion of nonspecific binding limit its usefulness for the in vivo quantification of 5-HT{sub 2A} receptors with PET.

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...

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)

A novel UV-emitting phosphor: LiSr4(BO3)3: Pb2+

International Nuclear Information System (INIS)

Pekgözlü, İlhan

2013-01-01

Pure and Pb 2+ doped LiSr 4 (BO 3 ) 3 materials were prepared by a solution combustion synthesis method. The phase analysis of all synthesized materials were determined using the powder XRD. The synthesized materials were investigated using spectrofluorometer at room temperature. The excitation and emission bands of LiSr 4 (BO 3 ) 3 : Pb 2+ were observed at 284 and 328 nm, respectively. The dependence of the emission intensity on the Pb 2+ concentration for the LiSr 4 (BO 3 ) 3 were studied in detail. It was observed that the concentration quenching of Pb 2+ in LiSr 4 (BO 3 ) 3 is 0.005 mol. The Stokes shifts of LiSr 4 (BO 3 ) 3 : Pb 2+ phosphor was calculated to be 4723 cm –1 . -- Highlights: • A novel UV-emitting phosphor: LiSr 4 (BO 3 ) 3 : Pb 2+ ” synthesized for the first time. • The emission band of LiSr 4 (BO 3 ) 3 : Pb 2+ was observed at 328 nm upon excitation with 284 nm. • LiSr 4 (BO 3 ) 3 : Pb 2+ is a good phosphor for broadband UV application

Single-phased CaAl2Si2O8:Tm3+, Dy3+ white-light phosphors under ultraviolet excitation

International Nuclear Information System (INIS)

Yang, Penghui; Yu, Xue; Xu, Xuhui; Jiang, Tingming; Yu, Hongling; Zhou, Dacheng; Yang, Zhengwen; Song, Zhiguo; Qiu, Jianbei

2013-01-01

A novel white-light-emitting phosphor CaAl 2 Si 2 O 8 :Tm, Dy was synthesized in ambient atmosphere by solid-state reaction. The energy transfer from Tm 3+ to Dy 3+ ions via a dipole–quadrupole reaction was observed and investigated. Upon UV excitation, white light emission was achieved by integrating a blue emission band located at 455 nm and an orange one located at 574 nm attributed to Tm 3+ and Dy 3+ ions, respectively. In addition, the energy-transfer efficiency and critical distance were calculated. Results suggested that the phosphor might be promising as a single-phased white-light-emitting phosphor for UV white-light LED. - Graphical abstract: The results indicate the existence of energy transfer from Tm 3+ to Dy 3+ . By tuning the concentration of Dy 3+ , single-phased white light can be realized. - Highlights: ► Energy transfer from Tm 3+ to Dy 3+ was investigated. ► Color tunable from blue to white can be achieved. ► White light can be realized in CaAl 2 Si 2 O 8 :Tm 3+ , Dy 3+ phosphor

On the application of CaF2:Eu and SrF2:Eu phosphors in LED based phototherapy lamp

Science.gov (United States)

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

2013-06-01

In the last few years the interest of scientific community has been increased towards solid state lighting based on LEDs because of their superior advantages over the conventional fluorescent lamps. As the GaN based LEDs are easily available efforts of the researchers are now on making the new phosphors which are excitable in the near UV region (360-400nm) for solid state lighting. This paper reports the photoluminescence characteristics of CaF2:Eu and SrF2:Eu phosphor prepared by wet chemical method. The violet emission of these phosphors with near UV excitation can be useful in making a phototherapy lamp based on LEDs for treating various skin diseases like acne vulgaris and hyperbilirubinemia.

Crystal structure of bis[μ-S-hexyl 3-(2-oxidobenzylidenedithiocarbazato-κ4O,N3,S:O]dicopper(II

Directory of Open Access Journals (Sweden)

M. S. Begum

2015-12-01

Full Text Available The title compound, [Cu2(C14H18N2OS22], is a binuclear copper(II complex of an oxybenzylidenedithiocarbazate ligand. The ligand coordinates in a tridentate manner through N-, S- and O-donor atoms. Each O atom also bridges to a second CuII ion to form the binuclear species. It has a central Cu2O2 rhomboid moiety and a metal-to-metal separation of 2.9923 (6 Å. In the crystal, the binuclear complexes stack along the a axis with all the hexyl chains located side-by-side, forming a hydrophobic region. The complexes are linked via C—H...N hydrogen bonds, forming chains along the c-axis direction. One CuII atom has the S atom of a symmetry-related complex located approximately in the apical position at 2.9740 (11 Å. This weak interaction links the chains to form slabs parallel to the ac plane.

Photoluminescence properties of blue light excited Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:Eu{sup 3+} red phosphors

Energy Technology Data Exchange (ETDEWEB)

Fang, Yongzheng; Liu, Fengxin; Hou, Jingshan; Zhang, Yan; Zheng, Xinfeng; Zhang, Na [School of Materials Science and Engineering, Shanghai Institute of Technology, Shanghai 201418 (China); Zhao, Guoying, E-mail: zhaogy135@sit.edu.cn [School of Materials Science and Engineering, Shanghai Institute of Technology, Shanghai 201418 (China); Liao, Meisong [Key Laboratory of Materials for High Powder Laser, Shanghai Institute of Optics and Fine Mechanics, Chinese Academy of Sciences, Shanghai 201800 (China); Dai, Guozhang; Long, Mengqiu [School of Physics and Electronics, Central South University, Changsha, Hunan 410083 (China); Liu, Yufeng, E-mail: yfliu@mail.sitp.ac.cn [School of Materials Science and Engineering, Shanghai Institute of Technology, Shanghai 201418 (China)

2016-09-15

A series of red emitting Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:xEu{sup 3+} (0≤x≤0.4) phosphors were synthesized by the conventional solid state reaction, and their photoluminescence properties were investigated in this work. Upon excitation of blue light, the Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:xEu{sup 3+} phosphors exhibit strong red emission at 616 nm, which corresponds to the dominant transition of Eu{sup 3+} ions in Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2} host, originating from the electric dipole transition {sup 5}D{sub 0}–{sup 7}F{sub 2}. Moreover, Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:0.3Eu{sup 3+} phosphor shows more intense photoluminescence than that of other phosphors, where the concentration of Eu{sup 3+} ion is not equal to 0.3. The CIE chromaticity coordinate (0.657, 0.343) of Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:0.3Eu{sup 3+} phosphor is close to National Television Standard Committee standard value (0.670, 0.330) of red phosphors, which indicates Ca{sub 8}La{sub 2}(PO{sub 4}){sub 6}O{sub 2}:0.3Eu{sup 3+} is potential to apply in white light-emitting diodes as an excellent red emitting phosphor.

Thermoluminescence properties of Eu-doped and Eu/Dy-codoped Sr2 Al2 SiO7 phosphors.

Science.gov (United States)

Jadhaw, Akhilesh; Sonwane, Vivek D; Gour, Anubha S; Jha, Piyush

2017-11-01

We report the thermoluminescence properties of Sr 1.96 Al 2 SiO 7 :Eu 0.04 and Sr 1.92 Al 2 SiO 7 :Eu 0.04 Dy 0.04 phosphors. These phosphors were prepared by a high-temperature solid-state reaction method. The prepared phosphors were characterized by X-ray diffraction. A 254 nm source was used for ultraviolet (UV) irradiation and a 60 Co source was used for γ-irradiation. The effect of heating rate and UV-exposure were examined. The thermoluminescence temperature shifts to higher values with increasing heating rate and thermoluminescence intensity increases with increasing UV exposure time. The trapping parameters such as activation energy (E), order of kinetics and frequency factor (s) were calculated by peak shape method. The effect of γ- and UV-irradiation on thermoluminescence studies was also examined. Copyright © 2017 John Wiley & Sons, Ltd.

LC/MS study of the UV filter hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]-benzoate (DHHB) aquatic chlorination with sodium hypochlorite.

Science.gov (United States)

Grbović, G; Trebše, P; Dolenc, D; Lebedev, A T; Sarakha, M

2013-11-01

The fate of modern personal care products in the environment is becoming a matter of increasing concern because of the growing production and assortment of these compounds. More and more chemicals of this class are treated as emerging contaminants. Transformation of commercially available products in the environment may result in the formation of a wide array of their metabolites. Personal care products in swimming pools and in drinking water reservoirs may undergo oxidation or chlorination. There is much data on the formation of more toxic metabolites from original low toxicity commercial products. Therefore, reliable identification of all possible transformation products and a thorough study of their physicochemical and biological properties are of high priority. The present study deals with the identification of the products of the aquatic chlorination of the hexyl 2-[4-(diethylamino)-2-hydroxybenzoyl]-benzoate ultraviolet filter. High-performance liquid chromatography/mass spectrometry (HPLC/MS) and HPLC/MS/MS with accurate mass measurements were used for this purpose. As a result, three chlorinated transformation products were identified. Copyright © 2013 John Wiley & Sons, Ltd.

Hyperfine interactions of a muoniated ethyl radical in supercritical CO2

International Nuclear Information System (INIS)

Cormier, Philip; Taylor, Becky; Ghandi, Khashayar

2009-01-01

A muoniated ethyl radical was studied in supercritical carbon dioxide. The muon and the proton hyperfine coupling constants were measured over temperatures ranging from 305 to 475 K, and a density range from 0.2 to 0.7 (g cm -3 ). A decrease was found in the muon hyperfine coupling constants as a function of the density, which can be attributed to the interaction between the CO 2 molecule and the p-orbital of the ethyl radical. The changes to the α-proton and β-proton hyperfine coupling constants with density are attributed to changes in the overall geometry in the formed radical. This system was modeled using quantum calculations.

Combustion synthesis of CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors in a closed system

Energy Technology Data Exchange (ETDEWEB)

Peng Wenfang; Zou Shaoyu; Liu Guanxi; Xiao Quanlan; Zhang Rui; Xie Lijuan; Cao Liwei [Department of Chemistry, Jinan University, Guangzhou 510632 (China); Meng Jianxin, E-mail: tmjx@jnu.edu.cn [Institute of Nano-Chemistry, Jinan University, Guangzhou 510632 (China); Liu Yingliang [Institute of Nano-Chemistry, Jinan University, Guangzhou 510632 (China)

2011-06-09

Highlights: > CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors can be prepared by a single-step combustion method. > The ignition temperature is the lowest in the combustion synthesis of Ce{sup 3+}/Eu{sup 2+} doped phosphors. > The as-prepared nano-phosphors give a uniform particle size in the range of 15-20 nm and have highly dispersity and fluorescence intensity. > It is a convenient method for preparation of monodispersed oxide nano-phosphors, especially those being sensitive to air at high temperature. - Abstract: The CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors were successfully prepared by a single-step combustion method at an ignition temperature as low as 200 deg. C in a closed autoclave using glycine as a fuel and PEG4000 as a dispersant. The samples were characterized by X-ray diffraction (XRD), photoluminescence (PL) spectroscopy, scanning electron microscopy (SEM) and transmission electron microscope (TEM). The results revealed that CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors can be conveniently prepared at an ignition temperature as low as 200 deg. C, which was much lower than that in the ordinary combustion methods. The optimized ignition temperature was 220 deg. C. The CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors give a uniform particle size in the range of 15-20 nm. The low ignition temperature and the addition of PEG4000 dispersant play important roles in the formation of small sized nanoparticles. The as-prepared nano-phosphors were incompact aggregates, but highly dispersed nano-phosphors can be obtained after further ultrasonic treatment. The CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors give satisfactory luminescence characteristic benefiting from the closed circumstance, in which cerium atoms can be isolated from the oxidizing atmosphere and non-fluorescent Ce{sup 4+} ions can be ruled out. The present highly dispersed CaSc{sub 2}O{sub 4}:Ce{sup 3+} nano-phosphors with efficient fluorescence are promising in the field of biological labeling

White LED based on CaAl2Si2O8:Eu2+ Mn2+ phosphor and CdS/ZnS quantum dots

Science.gov (United States)

Shen, Changyu; Zhong, Chuan; Hou, Qianglong; Li, Ke

2011-02-01

Core/shell CdS/ZnS quantum dots (QDs) with the emission wavelength of 610nm, was synthesized by thermal deposition using cadmium oxide and selenium as precursors in a hot lauric acid and hexadecylamine trioctylphosphine oxide hybrid. CaAl2Si2O8:Eu2+ Mn2+ phosphor was synthesized by high-temperature solid state reaction at 1290 °C for 2 hours under the H2 reducing atmosphere, and X-ray powder diffraction analysis confirmed the formation of it. It has two emission bands peaking at 420 nm and 580nm originated from the transition 5d to 4f of Eu2+ and 4T1-6A1 of Mn2+, respectively. Blends of CaAl2Si2O8:Eu2+,Mn2+ phosphor and CdS/ZnS QDs exhibited the prominent spectral evolution with an increasing content of QDs. A hybrid white LED, which combines a blue LED with the blend of CaAl2Si2O8:Eu2+ Mn2+ phosphor and QDs with a weight ratio of 2:1, with the CIE coordinate of (0.3183, 0.3036) and CRI of 85 was obtained.

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...

Luminescent properties and energy transfer of CaO:Ce3+, Mn2+ phosphors for white LED

International Nuclear Information System (INIS)

Liu, Qipeng; Yin, Huijun; Liu, Tao; Wang, CuiQing; Liu, Riqiang; Lü, Wei; You, Hongpeng

2016-01-01

We have synthesized yellow–orange CaO:Ce 3+ ,Mn 2+ phosphors by solid-state reaction. Photoluminescence properties and energy transfer mechanism from Ce 3+ to Mn 2+ ions have been investigated. The Ce 3+ activated phosphors exhibit strong absorption in the range of 250–490 nm and a yellow emission centered at 554 nm. When Mn 2+ ions were codoped, CaO:Ce 3+ ,Mn 2+ phosphors exhibit yellow emission band of Ce 3+ as well as orange emission band centered at 600 nm of Mn 2+ . We observed an efficient energy transfer from Ce 3+ to Mn 2+ ions in CaO:Ce 3+ ,Mn 2+ , which was verified from the lifetime decay curves and was discussed by Dexter's energy transfer theory. The critical distance of the energy transfer from Ce 3+ to Mn 2+ ions has also been calculated to be 12.3 Å by spectral overlap methods following Dexter's theory and by concentration quenching mechanism to be 15.2 Å. Moreover, by combining the synthesized phosphors and InGaN blue chip (460 nm), warm-white light has been created.

Modeling granular phosphor screens by Monte Carlo methods

International Nuclear Information System (INIS)

Liaparinos, Panagiotis F.; Kandarakis, Ioannis S.; Cavouras, Dionisis A.; Delis, Harry B.; Panayiotakis, George S.

2006-01-01

The intrinsic phosphor properties are of significant importance for the performance of phosphor screens used in medical imaging systems. In previous analytical-theoretical and Monte Carlo studies on granular phosphor materials, values of optical properties, and light interaction cross sections were found by fitting to experimental data. These values were then employed for the assessment of phosphor screen imaging performance. However, it was found that, depending on the experimental technique and fitting methodology, the optical parameters of a specific phosphor material varied within a wide range of values, i.e., variations of light scattering with respect to light absorption coefficients were often observed for the same phosphor material. In this study, x-ray and light transport within granular phosphor materials was studied by developing a computational model using Monte Carlo methods. The model was based on the intrinsic physical characteristics of the phosphor. Input values required to feed the model can be easily obtained from tabulated data. The complex refractive index was introduced and microscopic probabilities for light interactions were produced, using Mie scattering theory. Model validation was carried out by comparing model results on x-ray and light parameters (x-ray absorption, statistical fluctuations in the x-ray to light conversion process, number of emitted light photons, output light spatial distribution) with previous published experimental data on Gd 2 O 2 S:Tb phosphor material (Kodak Min-R screen). Results showed the dependence of the modulation transfer function (MTF) on phosphor grain size and material packing density. It was predicted that granular Gd 2 O 2 S:Tb screens of high packing density and small grain size may exhibit considerably better resolution and light emission properties than the conventional Gd 2 O 2 S:Tb screens, under similar conditions (x-ray incident energy, screen thickness)

Photoluminescence and thermoluminescence characterization of Eu3+- and Dy3+ -activated Ca3(PO4)2 phosphor

International Nuclear Information System (INIS)

Nagpure, I.M.; Saha, Subhajit; Dhoble, S.J.

2009-01-01

Rare-earth-doped polycrystalline Ca 3 (PO 4 ) 2 :Eu, Ca 3 (PO 4 ) 2 :Dy and Ca 3 (PO 4 ) 2 :Eu,Dy phosphors prepared by a modified solid-state synthesis has been studied for its X-ray diffraction, thermoluminescence (TL) and photoluminescence (PL) characteristics. The PL emission spectra of the phosphor suggest the presence of Eu 3+ ion in Ca 3 (PO 4 ) 2 :Eu and Dy 3+ ion in Ca 3 (PO 4 ) 2 :Dy lattice sites. The TL glow curve of the Ca 3 (PO 4 ) 2 :Eu compounds has a simple structure with a prominent peak at 228 deg. C, while Ca 3 (PO 4 ) 2 :Dy peaking at 146 and 230 deg. C. TL sensitivity of phosphors are compared with CaSO 4 : Dy and found 1.52 and 1.20 times less in Ca 3 (PO 4 ) 2 :Eu and Ca 3 (PO 4 ) 2 :Dy phosphors, respectively. The Ca 3 (PO 4 ) 2 :Eu,Dy phosphors shows switching behavior under two different excitation wavelengths and enhancement in PL intensity of Dy 3+ ions were reported. The paper discusses the photoluminescence and thermoluminescence behavior of Eu 3+ and Dy 3+ ion in Ca 3 (PO 4 ) 2 hosts, it may be applicable to solid-state lighting as well as thermoluminescence dosimetry applications.

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.

Photometric estimation of plutonium in product solutions and acid waste solutions using flow injection analysis technique

International Nuclear Information System (INIS)

Dhas, A.J.A.; Dharmapurikar, G.R.; Kumaraguru, K.; Vijayan, K.; Kapoor, S.C.; Ramanujam, A.

1995-01-01

Flow injection analysis technique is employed for the measurement of plutonium concentrations in product nitrate solutions by measuring the absorbance of Pu(III) at 565 nm and of Pu(IV) at 470 nm, using a Metrohm 662 photometer, with a pyrex glass tube of 2 nm (ID) inserted in the light path of the detector serving as a flow cell. The photometer detector never comes in contact with radioactive solution. In the case of acid waste solutions Pu is first purified by extraction chromatography with 2-ethyl hexyl hydrogen 2 ethyl hexyl phosphonate (KSM 17)- chromosorb and the Pu in the eluate in complexed with Arsenazo III followed by the measured of absorbance at 665 nm. Absorbance of reference solutions in the desired concentration ranges are measured to calibrate the system. The results obtained agree with the reference values within ±2.0%. (author). 3 refs., 1 tab

Photonics of dyes molecules in reverse micellar solution

International Nuclear Information System (INIS)

Ibragimova, M.R.; Laurinas, V.Ch.

2001-01-01

Spectral luminescent characteristics of the dye acridine orange and eosin has been studied in reverse micellar solutions of sodium bis(2-ethyl-hexyl)sulfosuccinate. It was shown that the increase of the nucleus volume of reverse micelles. (author)

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.

49 CFR 173.322 - Ethyl chloride.

Science.gov (United States)

2010-10-01

... 49 Transportation 2 2010-10-01 2010-10-01 false Ethyl chloride. 173.322 Section 173.322 Transportation Other Regulations Relating to Transportation PIPELINE AND HAZARDOUS MATERIALS SAFETY... SHIPMENTS AND PACKAGINGS Gases; Preparation and Packaging § 173.322 Ethyl chloride. Ethyl chloride must be...

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

Energy Technology Data Exchange (ETDEWEB)

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

2016-01-15

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

Consumption of Pt anode in phosphoric acid

Energy Technology Data Exchange (ETDEWEB)

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

1997-12-05

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

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.)

The preparation and characterization of uns-cis-(ethylene-diamine-N,N'-di-3-propionato(N-alkylethylenediaminescobalt(III complexes

Directory of Open Access Journals (Sweden)

SANJA R. GRGURIC

2000-03-01

Full Text Available Three octahedral cobalt(III complexes of the general formula uns-cis-SCo(eddp(R-enCClÿ2H2O, where eddp = the tetradentate ONNO-type ligand ethylenediamine-N,N'-di-3-propionate and R-en = a bidentate NN-type ligand, either N-methyl, N-ethyl or N-isopropylethylenediamine. The complexes were prepared by the reaction of sodium uns-cis-(ethylenediamine-N,N'-di-3-propionato(carbonatocobaltate(IIIdihydrate with the corresponding diamine. They were isolated chromatographically and characterized by elemental analysis, infrared and electronic absorption spectroscopy.

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

Directory of Open Access Journals (Sweden)

Raunak Kumar Tamrakar

2014-10-01

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

Equilibrium Model for the Extraction of Am(III), Eu(III), and HNO{sub 3} into DMDOHEMA in TPH

Energy Technology Data Exchange (ETDEWEB)

Geist, Andreas [Forschungszentrum Karlsruhe, Institut fuer Nukleare Entsorgung, P.O. Box 3640, 76021 Karlsruhe (Germany)

2008-07-01

The extraction of americium(III), europium(III), and nitric acid into DMDOHEMA (N,N'-dimethyl-N,N'-di-octyl-2-[2-hexyl-oxy-ethyl]-malonamide) dissolved in TPH (a kerosene-type diluent) was studied as a function of initial nitric acid and DMDOHEMA concentrations. Nitric acid extraction can be described by the formation of three complexes, HNO{sub 3}-L{sub 2}, HNO{sub 3}-L, and (HNO{sub 3}){sub 2}-L. Americium(III) extraction is best described by the formation of three complexes, Am(NO{sub 3}){sub 3}-L{sub 4}, Am(NO{sub 3}){sub 3}-HNO{sub 3}-L{sub 3}, and Am(NO{sub 3}){sub 3}-(HNO{sub 3}){sub 2}-L{sub 2}. However, some deviations occur at higher nitric acid concentrations. These deviations may be explained by the simplified but questionable assumption of constant activity coefficients in the organic phase. (author)

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

International Nuclear Information System (INIS)

Gu Yunxin; Zhang Qinghong; Wang Hongzhi; Li Yaogang

2009-01-01

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

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.

Photoluminescence properties of a novel red phosphor Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+}

Energy Technology Data Exchange (ETDEWEB)

Wang, Zhonghua; Hu, Yihua; Zhang, Shaoan; Lin, Jun [Guangdong University of Technology, School of Physics and Optoelectronic Engineering, Guangzhou (China)

2016-02-15

Eu{sup 3+}-doped Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2} phosphors were synthesized successfully via a two-step solid-state reaction method. Phase purity and morphology of the phosphor were confirmed by XRD and SEM techniques. In the excitation spectra of Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} phosphor, the broad excitation band centering at 310 nm is due to the combination of charge transfer from Eu{sup 3+}→O{sup 2-} and host absorption. And it matches well the emission wavelength from UV LEDs. Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} phosphors show a bright orange-red luminescence under excitation with 301 nm. However, concentration quenching of Eu{sup 3+} in Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} occurs at a low content of 0.07 in this work. The quenching mechanism of Sr{sub 3}Ga{sub 2}O{sub 5}Cl{sub 2}:Eu{sup 3+} was discussed in detail on the basis of the experimental results. (orig.)

Enhancement of Color Rendering Index for White Light LED Lamps by Red Y2O3:EU3+ Phosphor

Directory of Open Access Journals (Sweden)

Tran Hoang Quang Minh

2016-01-01

Full Text Available We present an application of the red Y2O3:Eu3+ dopant phosphor compound for reaching the color rendering index as high as 86. The Multi-Chip White LED lamps (MCW-LEDs with high Correlated Color Temperatures (CCTs including 7000 K and 8500 K are employed in this study. Besides, the impacts of the Y2O3:Eu3+ phosphor on the attenuation of light through phosphor layers of the various packages is also demonstrated based on the Beer-Lambert law. Simulation results provide important conclusion for selecting and developing the phosphor materials in MCW-LEDs manufacturing.

Luminescent properties of Mg3Ca3(PO4)4: Eu2+ blue-emitting phosphor for white light emitting diodes

International Nuclear Information System (INIS)

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

2012-01-01

A blue-emitting phosphor, Eu 2+ -activated Mg 3 Ca 3 (PO 4 ) 4 phosphor was synthesized by conventional solid-state reaction. X-ray powder diffraction (XRD) analysis confirmed the phase formation. Photoluminescence (PL) results showed that Mg 3 Ca 3 (PO 4 ) 4 : Eu 2+ could be efficiently excited by UV–visible light from 250 to 430 nm, which matched well with the emission wavelengths of near-UV and UV LED chips. The effects of the doped-Eu 2+ concentration in Mg 3 Ca 3 (PO 4 ) 4 : Eu 2+ on the PL were also investigated. The result reveals that Mg 3 Ca 3 (PO 4 ) 4 : Eu 2+ is a potential blue-emitting phosphor for white LEDs. - Graphical Abstract: The excitation spectra show a broad peak from 250 to 430 nm, which means Mg 3 Ca 3 (PO 4 ) 4 : Eu 2+ phosphor can be suitable for application in white LEDs excited by the near-UV and UV LEDs. The emission spectrum peaked at 456 nm with the full-width half-maximum (FWHM) of 102 nm is attributed to the 4f 6 5d 1 –4f 7 transition of the Eu 2+ ion. The asymmetric emission spectra show that Eu 2+ has more one emission center in Mg 3 Ca 3 (PO 4 ) 4 , which can be deconvoluted into at least four Gaussian components peaked at 423, 446, 483 and 510 nm. Highlights: ► Mg 3 Ca 3 (PO 4 ) 4 : Eu 2+ phosphor could be effectively excited by UV chips (360–430 nm). ► Mg 3 Ca 3 (PO 4 ) 4 : Eu 2+ phosphor is a potential blue-emitting phosphor for white LEDs. ► Mg 3 Ca 3 (PO 4 ) 4 : Eu 2+ phosphor shows a broadband emission.

Preparation and luminescence properties of Ce3+ and Ce3+/Tb(3+)-activated Y4Si2O7N2 phosphors.

Science.gov (United States)

Xia, Zhiguo; Wu, Weiwei

2013-09-28

Ce(3+) and Ce(3+)/Tb(3+)-activated Y4Si2O7N2 phosphors are synthesized by the solid-state method, which can be efficiently excited by near ultraviolet (UV) light emitting diode (LED) chips. The PL spectrum of Y4Si2O7N2:Ce(3+) shows a broad hump between 380 and 650 nm, assigned to the electron transition from the 4f energy level to different 5d sub levels of the Ce(3+) ions at different Y(3+) sites. The color of the Y4Si2O7N2:Ce(3+) phosphor can shift from blue to green by introducing Tb(3+). In addition, the energy transfer process from Ce(3+) to Tb(3+) in the Y4Si2O7N2 host was investigated and discussed in terms of both the luminescence spectra and decay curves. The energy transfer critical distance has been calculated and evaluated by the concentration quenching method. Therefore, the Ce(3+) and Ce(3+)/Tb(3+)-activated Y4Si2O7N2 phosphors can serve as key materials for phosphor-converted white-light UV-LEDs.

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.

The photoluminescent properties of Y2O3:Bi3+, Eu3+, Dy3+ phosphors for white-light-emitting diodes.

Science.gov (United States)

Han, Xiumei; Feng, Xu; Qi, Xiwei; Wang, Xiaoqiang; Li, Mingya

2014-05-01

Bi3+, Eu3+, Dy3+ activated Y2O3 phosphors were prepared through the sol-gel process. X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectra, and photoluminescence (PL) spectra were used to characterize the resulting phosphors. The XRD patterns show the refined crystal structure of Y2O3. The energy transfer processes of Bi(3+)-Eu3+ occurred in the host lattices. The thermal stability of Y2O3:Bi3+, Eu3+, Dy3+ phosphors was studied. Under short wavelength UV excitation, the phosphors show excellent characteristic red, blue, and yellow emission with medium intensity.

Synthesis and photoluminescence properties of Ba2CaZn2Si6O17:Eu3+ red phosphors for white LED applications

International Nuclear Information System (INIS)

Annadurai, G.; Kennedy, S. Masilla Moses

2016-01-01

Novel pellyite type Ba 2 CaZn 2 Si 6 O 17 :Eu 3+ red emitting phosphors with different Eu 3+ contents were synthesized by the solid state reaction method. The crystal structure, photoluminescence properties and concentration quenching of Ba 2 CaZn 2 Si 6 O 17 :Eu 3+ phosphors were investigated. Powder X-ray diffraction measurements confirmed the structure of the samples. The photoluminescence emission (PL) and excitation (PLE) spectra were measured. The results showed that the dominant hypersensitive red emission peak of the phosphors Ba 2 CaZn 2 Si 6 O 17 :Eu 3+ was located at 613 nm attributed to the Eu 3+ transition ( 5 D 0 → 7 F 2 ) which could be effectively excited by 395 nm (near-UV). The latter band matched well with the emission from the near-UV LED chips. The intensity ratio of 5 D 0 → 7 F 2 to 5 D 0 → 7 F 1 transition showed slight variation with Eu 3+ concentrations. The Eu 3+ emission intensity was maximum for 9 mol%. The luminescence quantum efficiency was determined and also the decay profiles were obtained and analyzed. In addition, the Commission International del'Eclairage (CIE) chromaticity coordinates of Ba 2 CaZn 2 Si 6 O 17 :0.09Eu 3+ phosphor were calculated to be 0.637 and 0.362. The experimental results demonstrated that the Ba 2 CaZn 2 Si 6 O 17 :Eu 3+ red emitting phosphor is a potential candidate for white light emitting diodes (WLEDs) pumped by near-UV chip. - Highlights: • A novel Ba 2 CaZn 2 Si 6 O 17 :Eu 3+ red phosphor was synthesized. • The samples yielded a dominant PL emission of Eu 3+ at 613 nm. • Eu 3+ concentration was optimized to be 9 mol% in Ba 2 CaZn 2 Si 6 O 17. • CIE chromaticity coordinates were estimated from the emission spectrum.

Intense blue upconversion emission and intrinsic optical bistability in Tm3+/Yb3+/Zn2+ tridoped YVO4 phosphors

Science.gov (United States)

Yadav, Manglesh; Mondal, Manisha; Mukhopadhyay, Lakshmi; Rai, Vineet Kumar

2018-04-01

Tm3+/Yb3+/Zn2+:yttrium metavanadate (YVO4) phosphors prepared through chemical coprecipitation and the solid state reaction method have been structurally characterized by an x-ray diffraction (XRD) study. Photoluminescence study of the developed phosphors under ultraviolet (UV) and near infrared (NIR) excitation has been performed. The excitation spectrum of the tetragonal zircon type YVO4 phosphors corresponding to the emission at ˜476 nm exhibits a broad excitation peak in the 250-350 nm region, which is due to charge distribution in the {{{{VO}}}4}3- group. Under 980 nm CW diode laser excitation, enhancements of about ˜3000 times and ˜40 times have been observed for the blue band in the tridoped Tm3+Yb3+Zn2+:YVO4 phosphors compared to those of the Tm3+:YVO4 singly and Tm3+/Yb3+:YVO4 codoped phosphors, respectively. A downconversion (DC) emission study shows an enhancement of about ˜50 times for the blue band in the tridoped phosphors compared to that of the singly doped phosphors. Optical bistability (OB) behavior of the developed phosphors has been also investigated upon 980 nm excitation. The calculated Commission Internationale de l’Éclairage (CIE) color coordinates lie in the blue region with 96.5% color purity under 980 nm excitation, having a color temperature of ˜3400 K. Our observations show that the developed phosphors may be suitably used in dual mode luminescence spectroscopy, display devices, and UV LED chips.

Discovery of novel solid solution Ca3Si3-x O3+x N4-2x : Eu2+ phosphors: structural evolution and photoluminescence tuning.

Science.gov (United States)

Wang, Baochen; Liu, Yan-Gai; Huang, Zhaohui; Fang, Minghao; Wu, Xiaowen

2017-12-22

Discovery of novel phosphors is one of the main issues for improving the color rendering index (CRI) and correlated color temperature (CCT) of white light-emitting diodes (w-LEDs). This study mainly presents a systematic research on the synthesis, crystal structure variation and photoluminescence tuning of novel (oxy)nitride solid solution Ca 3 Si 3-x O 3+x N 4-2x : Eu 2+ phosphors. XRD refinements show that lattice distortion occurs when x value diverges the optimum one (x = 1). The lattice distortion causes a widening of emission spectrum and an increase of Stokes shift (ΔSS), which leads to a bigger thermal quenching. With decrease of x value, the emission spectrum shows an obvious red-shift from 505.2 to 540.8 nm, which is attributed to the crystal field splitting. The enhanced crystal field splitting also broadens the excitation spectrum, making it possible to serve as the phosphor for near ultraviolet (n-UV) LEDs. A 3-phosphor-conversion w-LED lamp was fabricated with the as-prepared phosphor, which exhibits high CRI (Ra = 85.29) and suitable CCT (4903.35 K). All these results indicate that the Ca 3 Si 3-x O 3+x N 4-2x : Eu 2+ phosphor can serve as the green phosphor for n-UV w-LEDs, with a tunable spectrum by controlling the crystal structure and morphology.

21 CFR 172.515 - Synthetic flavoring substances and adjuvants.

Science.gov (United States)

2010-04-01

.... 3-Octanol. 2-Octanone; methyl hexyl ketone. 3-Octanone; ethyl amyl ketone. 3-Octanon-1-ol. 1-Octen-3...; isodecylaldehyde. 3,7-Dimethyl-1-octanol; tetrahydrogeraniol. α,α-Dimethylphenethyl acetate; benzylpropyl acetate...)-nonanamide; pelargonyl vanillylamide. 5-Hydroxy-4-octanone; butyroin. 4-(p-Hydroxyphenyl)-2-butanone; p-hy...

Synthesis of enantiomerically pure (R)- and (S)-2-sulfanylpropanoic acids (‘thiolactic acid’) from ethyl (S)-lactate using pig liver esterase

NARCIS (Netherlands)

Hof, Robert P.; Kellogg, Richard M.

1995-01-01

The methanesulfonates of optically pure ethyl (S)-lactate or ethyl (R)-2-chloropropanoate 5, obtained with inversion of configuration from ethyl (S)-lactate on treatment with SOCl2, can be substituted by caesium thiolates with inversion of configuration to yield (R) and (S) ethyl

BaFCl:Eu2+, a new phosphor for X-ray-intensifying screens

International Nuclear Information System (INIS)

Stevels, A.L.N.; Pingault, F.

1975-01-01

A number of phosphors for X-ray-intensifying screens have been evaluated by calculating figures of merit. On use in combination with standard (''blue''-sensitive) X-ray film, BaFCl:Eu 2+ and BaFBr:Eu 2+ give better performance than the traditional CaWO 4 and more recently developed UV or blue-emitting materials (e.g., sulphates and y-oxysulphides). The calculated figures of merit of BaFCl:Eu 2+ or BaFBr:Eu 2+ /standard-film combinations are comparable to those of Gd 2 O 2 S:Tb/green-sensitive X-ray film systems. The preparation of optimal fluorohalide:Eu 2+ phosphors involves proper formation of the host lattice, complete reduction of Eu 3+ ions as well as elimination of afterglow. Measurements on powders and experimental screens indicate that by using BaFCl:Eu 2+ screens in radiography, important dose reductions can be achieved without the necessity of using other than standard (''blue''-sensitive) X-ray films

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.

Synthesis and Crystal Structure of Di-μ-chlorido-bis{chlorido[4-ethyl- N-(pyridin-2-ylmethylidene-κ N)aniline-κ N]mercury(II)}

Science.gov (United States)

Khalaj, M.; Seftejani, F. B.; Ghazanfarpour-Darjani, M.; Lalegani, A.

2017-12-01

The centrosymmetric dinuclear title complex [Hg2Cl4(dip)2] was synthesized using the Schiff base bidentate ligand (E)-4-ethyl- N-(pyridine-2-ylmethylene)benzeneamine ( dip) and mercury(II) chloride salts. It has been characterized by elemental analysis, X-ray diffraction, and UV-Visible and infrared spectroscopic techniques. The X-ray analysis shows that the title compound crystallizes in the monoclinic sp. gr. P21/n, Z = 2 with a = 7.8233(17) Å, b = 15.178(3) Å, c = 12.559(3) Å, β = 97.021(3)°. The Hg(II) ion has a distorted trigonal-bipyramidal coordination environment formed by the bischelating N-heterocyclic ligands, two bridging Cl atoms and one terminal Cl atom.

Ultrathin regioregular poly(3-hexyl thiophene) field-effect transistors

DEFF Research Database (Denmark)

Sandberg, H.G.O.; Frey, G.L.; Shkunov, M.N.

2002-01-01

Ultrathin films of regioregular poly(3-hexyl thiophene) (RR-P3HT) were deposited through a dip-coating technique and utilized as the semiconducting film in field-effect transistors (FETs). Proper selection of the substrate and solution concentration enabled the growth of a monolayer-thick RR-P3HT...... film. Atomic force microscopy (AFM), U-V-vis absorption spectroscopy, X-ray reflectivity, and grazing incidence diffraction were used to study the growth mechanism, thickness and orientation of self-organized monolayer thick RR-P3HT films on SiO2 surfaces. Films were found to adopt a Stranski......-Krastanov-type growth mode with formation of a very stable first monolayer. X-ray measurements show that the direction of pi-stacking in the films (the (010) direction) is parallel to the substrate, which is the preferred orientation for high field-effect carrier mobilities. The field-effect mobilities in all ultrathin...

Properties–structure relationship research on LiCaPO4:Eu2+ as blue phosphor for NUV LED application

International Nuclear Information System (INIS)

Zhang, Xinguo; Mo, Fuwang; Zhou, Liya; Gong, Menglian

2013-01-01

Graphical abstract: The graphical abstract shows the excitation and emission spectrum of LiCaPO 4 :Eu 2+ , and the CIE coordinates of LiCaPO 4 :Eu 2+ . The inset shows the photo of blue LED prepared by LiCaPO 4 :Eu 2+ and NUV chip. It indicates that this phosphor can be excited by UV light and emit strong greenish-blue light. Highlights: •Pure phase blue phosphors of LiCaPO 4 :Eu 2+ with a hexagonal structure were first prepared via solid-state method. •The crystallographic site of Eu 2+ ion in the LiCaPO 4 lattice was identified as 8-fold Ca 2+ site. •The phosphor exhibits excellent thermal stability and the corresponding mechanism was thermal assisted ionization. •Bright and high color purity blue LED prototype based on LiCaPO 4 :Eu 2+ phosphor was fabricated. -- Abstract: Blue-emitting phosphors of Eu 2+ -activated LiCaPO 4 with a hexagonal structure were prepared via a conventional solid-state method. The XRD, PL spectra and thermal quenching were applied to characterize the phosphors. The crystallographic site of Eu 2+ ion in the LiCaPO 4 lattice was identified and discussed. The optimized LiCaPO 4 :0.03Eu 2+ exhibits the bright greenish-blue emission with CIE coordinates of (0.119, 0.155) and a quantum efficiency of 52%. The critical energy-transfer distance was confirmed as ∼18 Å by both calculated crystal structure method and experimental spectral method. The thermal stability of LiCaPO 4 :Eu 2+ was evaluated by temperature-dependent PL spectra, and the thermal quenching mechanism was found to be thermal assisted ionization. Prototype blue LEDs with high color purity and good current stability were fabricated

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.

Tricolor emission Ca3Si2O7:Ln (Ln=Ce, Tb, Eu) phosphors for near-UV white light-emitting-diode

International Nuclear Information System (INIS)

Mao, Zhi-yong; Zhu, Ying-chun; Gan, Lin; Zeng, Yi; Xu, Fang-fang; Wang, Yang; Tian, Hua; Li, Jian; Wang, Da-jian

2013-01-01

Tricolor emission in a same Ca 3 Si 2 O 7 host with independent Ln (Ln=Ce 3+ , Eu 2+ , Tb 3+ ) dopants is demonstrated to construct a near-UV white light emitting diode (LED). The luminescence properties and thermal quenching properties, as well as the applications in near-UV white LED are investigated. These phosphors show typical blue, red, and green, three-basal-color, luminescence in the CIE chromaticity diagram for Ce 3+ , Eu 2+ and Tb 3+ dopants, respectively. Thermal quenching properties show that the luminescence thermal stability strongly depends on the different dopant types; better thermal quenching property of Ce 3+ and Tb 3+ is recorded in comparison with that of Eu 2+ . The white LED prototype fabricated with near-UV chip and as-prepared tricolor phosphors exhibits acceptable CIE chromaticity coordinates (0.32, 0.30) with a CCT of 6000 K and a CRI of 87, indicating the potential application of Ca 3 Si 2 O 7 :Ln phosphors in near-UV white LED. - Highlights: ► Tricolor Ca 3 Si 2 O 7 : Ln phosphors were demonstrated to construct near-UV white LED. ► Eu 2+ doped Ca 3 Si 2 O 7 red-emitting phosphor was confirmed by this work once again. ► Thermal quenching properties for Ca 3 Si 2 O 7 :Ln phosphors were reported for the first time. ► Performances of fabricated white LED indicated the potential application of phosphors.

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

Science.gov (United States)

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

2015-06-01

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

Atom transfer radical polymerization of n-butyl acrylate catalyzed by atom transfer radical polymerization of n-butyl acrylate catalyzed by

NARCIS (Netherlands)

Zhang, H.; Linde, van der R.

2002-01-01

The homogeneous atom transfer radical polymerization (ATRP) of n-butyl acrylate with CuBr/N-(n-hexyl)-2-pyridylmethanimine as a catalyst and ethyl 2-bromoisobutyrate as an initiator was investigated. The kinetic plots of ln([M]0/[M]) versus the reaction time for the ATRP systems in different

Optimization of CeO2-ZrO2 mixed oxide catalysts for ethyl acetate combustion

Czech Academy of Sciences Publication Activity Database

Dimitrov, M.; Ivanova, R.; Štengl, Václav; Henych, Jiří; Kovacheva, D.; Tsoncheva, T.

2015-01-01

Roč. 47, č. 1 (2015), s. 323-329 ISSN 0324-1130 Institutional support: RVO:61388980 Keywords : nanosized CeO2-ZrO2 * mixed oxide phase * ethyl acetate combustion Subject RIV: CA - Inorganic Chemistry Impact factor: 0.229, year: 2015

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

Synthesis and photoluminescence properties of LiSrPO{sub 4}:Eu{sup 2+} phosphor for solid state lighting

Energy Technology Data Exchange (ETDEWEB)

Game, D. N., E-mail: deorao.game@gmail.com [Deccan Education Society’s Technical Institute, Fergusson College Campus, Pune (India); Taide, S. T.; Khan, Z. S.; Omanwar, S. K. [Department of Physics, Sant Gadge Baba, Aravati University, Amravati (India); Ingale, N. B. [Prof. Ram Meghe Institute of Technology and Research, Badnera, Amravati (India)

2016-05-06

A novel method to prepare orthophosphate LiSrPO{sub 4}: Eu{sup 2+} phosphor for white light-emitting diodes (w-LEDs) is given in this paper. Phosphor was successfully synthesized by Pechini (citrate gel) method which is efficient than conventional high temperature solid state reaction. X-ray powder diffraction (XRD) analysis confirmed the single phase formation of LiSrPO{sub 4}:Eu{sup 2+} with monoclinic crystal structure. Luminescence results showed that the phosphor could be efficiently excited by near UV and exhibited bright blue emission at λ{sub em} = 420 nm corresponding to 5d– 4f transition of Eu{sup 2+}. The phosphor exhibits blue emission bands under 350 nm excitation. This mercury-free excitation is useful for solid state lighting and light-emitting diode (LED). Hence it could be useful for solid state lighting and light-emitting diode (LED) application.

Synthesis, electronic structure and luminescent properties of a new red-emitting phosphor GdBiW2O9:Eu3+

Science.gov (United States)

Xie, Zhi; Zhou, Weiwei; Zhao, Wang; Zhang, Hao; Hu, Qichang; Xu, Xuee

2017-10-01

Red phosphor of GdBiW2O9:Eu3+ was prepared by solid-state reaction method. The phase purity and structure of the samples were characterized by XRD. The electronic structures of GdBiW2O9 host were estimated by DFT calculation. The PLE and PL spectra were also investigated. The optimal luminescent properties of GdBiW2O9:Eu3+ phosphors were obtained at 900 °C with 40 mol% of Eu3+ concentration. The phosphors can be excited efficiently by 396 nm NUV light and emit intense red light peaking at 618 nm. The results indicate GdBiW2O9:Eu3+ can act as a potential red-emitting phosphor for LEDs application.

Energy transfer and tunable luminescence of Na{sub 2}(Y,Eu)Mg{sub 2}V{sub 3}O{sub 12} phosphors for white LED applications

Energy Technology Data Exchange (ETDEWEB)

Zheng, Zhang; Wanjun, Tang, E-mail: tangmailbox@126.com

2016-01-15

Highlights: • Iso-structural garnet-type Na{sub 2}(Y,Eu)Mg{sub 2}V{sub 3}O{sub 12} solid solution were synthesized. • Efficient energy transfer from [VO{sub 4}]{sup 3−} to Eu{sup 3+} ions in this phosphor is observed obviously. • Tuning the Y/Eu ratio generates the varied hues from yellowish-green to reddish-orange. • This kind of phosphor can be potentially used in UV pumped LEDs. - Abstract: A series of solid-solution phosphors Na{sub 2}(Y,Eu)Mg{sub 2}V{sub 3}O{sub 12} were prepared using solution combustion reaction. X-ray diffraction studies verified the formation of single phase Na{sub 2}(Y,Eu)Mg{sub 2}V{sub 3}O{sub 12} with garnet structure. Na{sub 2}(Y,Eu)Mg{sub 2}V{sub 3}O{sub 12} phosphors show not only a broad emission band with a maximum at 510 nm due to the [VO{sub 4}]{sup 3−} group but also several sharp emission lines due to the Eu{sup 3+} ions. The energy transfer from [VO{sub 4}]{sup 3−} to Eu{sup 3+} was discussed on the base of the spectral analysis. The color-tunable emissions of the Na{sub 2}(Y,Eu)Mg{sub 2}V{sub 3}O{sub 12} phosphor as a function of Y/Eu ratio are realized by continuously generating the varied hues from yellowish-green to reddish-orange. This indicates that the obtained phosphor may have potential applications in the field of UV-based white LEDs.

Hyperfine interactions of a muoniated ethyl radical in supercritical CO{sub 2}

Energy Technology Data Exchange (ETDEWEB)

Cormier, Philip; Taylor, Becky [Department of Chemistry, Mount Allison University, Sackville, New Brunswick, E4L 1G8 (Canada); Ghandi, Khashayar, E-mail: kghandi@mta.c [Department of Chemistry, Mount Allison University, Sackville, New Brunswick, E4L 1G8 (Canada)

2009-04-15

A muoniated ethyl radical was studied in supercritical carbon dioxide. The muon and the proton hyperfine coupling constants were measured over temperatures ranging from 305 to 475 K, and a density range from 0.2 to 0.7 (g cm{sup -3}). A decrease was found in the muon hyperfine coupling constants as a function of the density, which can be attributed to the interaction between the CO{sub 2} molecule and the p-orbital of the ethyl radical. The changes to the alpha-proton and beta-proton hyperfine coupling constants with density are attributed to changes in the overall geometry in the formed radical. This system was modeled using quantum calculations.

Ethyl 2-[1-(3-methylbutyl-4-phenyl-1H-1,2,3-triazol-5-yl]-2-oxoacetate

Directory of Open Access Journals (Sweden)

Muhammad Hafeez

2013-12-01

Full Text Available In the title compound, C17H21N3O3, the non-planar (r.m.s. deviation = 0.212 Å ethyl (oxoacetate group is oriented towards the phenyl substituent. The triazole and benzene rings are twisted with respect to each other, making a dihedral angle of 41.69 (6°. In the crystal, molecules are arranged into centrosymmetric R22(10 dimers via pairs of C—H...O interactions involving the ethyl (oxoacetate groups. In addition, the triazole rings show π–π stacking interactions, with their centroids at a distance of 3.745 (2 Å.

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

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+ .

Biomonitoring of N-ethyl-2-pyrrolidone in automobile varnishers.

Science.gov (United States)

Koslitz, Stephan; Meier, Swetlana; Schindler, Birgit Karin; Weiss, Tobias; Koch, Holger Martin; Brüning, Thomas; Käfferlein, Heiko Udo

2014-12-01

N-alkyl-2-pyrrolidones are important organic solvents for varnishes in industry. This study investigates exposure to N-ethyl-2-pyrrolidone (NEP) in varnishing of hard plastic components in an automobile plant. Two specific biomarkers of exposure, 5-hydroxy-N-ethyl-2-pyrrolidone (5-HNEP) and 2-hydroxy-N-ethylsuccinimide (2-HESI), were analyzed in urine samples of 14 workers. For this purpose, pre-shift, post-shift and next day pre-shift urine samples were collected midweek. Twelve workers performed regular work tasks (loading, wiping and packing), whereas two workers performed special work tasks including cleaning the sprayer system with organic solvents containing N-alkyl-2-pyrrolidones. Spot urine samples of nine non-exposed persons of the same plant served as controls. Median post-shift urinary levels of workers with regular work tasks (5-HNEP: 0.15 mg/L; 2-HESI: 0.19 mg/L) were ∼5-fold higher compared to the controls (0.03 mg/L each). Continuously increasing metabolite levels, from pre-shift via post-shift to pre-shift samples of the following day, were observed in particular for the two workers with the special working tasks. Maximum levels were 31.01 mg/L (5-HNEP) and 8.45 mg/L (2-HESI). No clear trend was evident for workers with regular working tasks. In summary, we were able to show that workers can be exposed to NEP during varnishing tasks in the automobile industry. Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Synthesis and luminescence properties of ZnAl{sub 2}O{sub 4}:RE{sup 3+} (RE = Eu, Sm) phosphors

Energy Technology Data Exchange (ETDEWEB)

Lee, Seung Jin; Cho, Shin Ho [Silla University, Busan (Korea, Republic of)

2014-01-15

ZnAl{sub 2}O{sub 4}:RE{sup 3+} (RE = Eu or Sm) phosphor powders were synthesized with different concentrations of activator ions by using the conventional solid-state reaction method. The effects of the concentration of activator ions on the structural, morphological, and luminescent properties of zinc aluminate phosphors were investigated. The X-ray diffraction patterns revealed that the phosphors synthesized with different concentrations of activator ions showed mixed phases of ZnAl{sub 2}O{sub 4}, ZnO, and Al{sub 2}O{sub 3}. The crystallite size was estimated using the Scherrer formula, and the maximum size was obtained for 0.20 mol of Eu{sup 3+} ions. The emission spectra of of Eu{sup 3+}-doped ZnAl{sub 2}O{sub 4} phosphors under excitation at 303 nm exhibited one intense green band at approximately 520 nm and three weak bands centered at 590, 621, and 701 nm, respectively. The intensity of all the emission bands reached a maximum for 0.05 mol of Eu{sup 3+} ions. For the Sm{sup 3+}-doped ZnAl{sub 2}O{sub 4} phosphors, a broad emission band peak at 526 nm and several weak lines in the range 470 - 700 nm were observed. The results suggest that the luminescent intensity of the phosphors can be enhanced by controlling the amount of activator ions incorporated into the host lattice.

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.)

Study on luminescence and thermal stability of blue-emitting Sr_5(PO_4)_3F: Eu"2"+phosphor for application in InGaN-based LEDs

International Nuclear Information System (INIS)

Liu, Jie; Zhang, Zhi-Ming; Wu, Zhan-Chao; Wang, Fang-Fang; Li, Zhen-Jiang

2017-01-01

Highlights: • A blue phosphor Sr_5(PO_4)_3F: Eu"2"+ was prepared at low temperature of 800 °C. • The broad excitation band of the phosphor matches well with NUV LED chips. • The phosphor shows high color purity and good color stability. • A bright blue-emitting LED was fabricated with this phosphor on an InGaN chip. - Abstract: A series of blue-emitting phosphors Sr_5(PO_4)_3F: Eu"2"+ were synthesized by traditional high temperature solid-state reaction method. The micro-morphology and photoluminescence properties of the phosphors were investigated. The Sr_5(PO_4)_3F: Eu"2"+ phosphors exhibit broad excitation spectra ranging from 250 to 420 nm, and an intense asymmetric blue emission band peaking at 435 nm. Two different Eu"2"+ emission centers in Sr_5(PO_4)_3F: Eu"2"+ phosphors were confirmed via their fluorescence properties. The concentration quenching mechanism, fluorescence lifetime and thermal stability of Sr_5(PO_4)_3F: Eu"2"+ phosphors were studied in detail. The thermal stability can be improved obviously by anion substitution. The CIE chromaticity coordinates of Sr_5(PO_4)_3F: Eu"2"+ phosphors with different Eu"2"+-doped concentrations were calculated. A blue light-emitting diode was fabricated by combination of a 370 nm InGaN chip and the prepared phosphor Sr_5(PO_4)_3F: Eu"2"+. The present work suggests that Sr_5(PO_4)_3F: Eu"2"+ is a potential phosphor applied in InGaN-based LEDs.

Synthesis and luminescent properties of CaCO3:Eu3+@SiO2 phosphors with core-shell structure

Science.gov (United States)

Liu, Min; Kang, Ming; Chen, Kexu; Mou, Yongren; Sun, Rong

2018-03-01

Integrating the processes of preparation of CaCO3:Eu3+ and its surface-coating, core-shell structured CaCO3:Eu3+@SiO2 phosphors with red emission were synthesized by the carbonation method and surface precipitation procedure using sodium silicate as silica source. The phase structure, thermal stability, morphology and luminescent property of the as-synthesized samples were characterized by X-ray diffraction, Fourier transform infrared spectrum, thermal analysis, field-emission scanning electron microscopy, transmission electron microscope and photoluminescence spectra. The experimental results show that Eu3+ ions as the luminescence center are divided into two types: one is at the surface of the CaCO3 and the other inhabits the site of Ca2+. For CaCO3:Eu3+@SiO2 phosphors, the SiO2 layers are continuously coated on the surface of CaCO3:Eu3+ and show a typical core-shell structure. After coated with SiO2 layer, the luminous intensity and the compatibility with the rubber matrix increase greatly. Additionally, the luminous intensity increases with the increasing of Eu3+ ions concentration in CaCO3 core and concentration quenching occurs when Eu3+ ions concentration exceeds 7.0 mol%, while it is 5.0 mol% for CaCO3:Eu3+ phosphors. Therefore, preparation of CaCO3:Eu3+@SiO2 phosphors can not only simplify the experimental process through integrating the preparation of CaCO3:Eu3+ and SiO2 layer, but also effectively increase the luminous intensities of CaCO3:Eu3+ phosphors. The as-obtained phosphors may have potential applications in the fields of optical materials and functional polymer composite materials, such as plastics and rubbers.

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

Energy Technology Data Exchange (ETDEWEB)

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

2015-06-01

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

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

International Nuclear Information System (INIS)

Pandey, Anurag; Kaushal Kumar; Rai, Vineet Kumar

2012-01-01

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

A survey of phosphors novel for thermography

Energy Technology Data Exchange (ETDEWEB)

Bruebach, J., E-mail: bruebach@ekt.tu-darmstadt.d [Fachgebiet Reaktive Stroemungen und Messtechnik, Center of Smart Interfaces Technische Universitaet Darmstadt, Petersenstrasse 32, 64287 Darmstadt (Germany); Kissel, T. [Fachgebiet Reaktive Stroemungen und Messtechnik, Center of Smart Interfaces Technische Universitaet Darmstadt, Petersenstrasse 32, 64287 Darmstadt (Germany); Frotscher, M. [Eduard-Zintl-Institut fuer Anorganische und Physikalische Chemie, Technische Universitaet Darmstadt, Petersenstrasse 18, 64287 Darmstadt (Germany); Euler, M. [Fachgebiet Reaktive Stroemungen und Messtechnik, Center of Smart Interfaces Technische Universitaet Darmstadt, Petersenstrasse 32, 64287 Darmstadt (Germany); Albert, B. [Eduard-Zintl-Institut fuer Anorganische und Physikalische Chemie, Technische Universitaet Darmstadt, Petersenstrasse 18, 64287 Darmstadt (Germany); Dreizler, A. [Fachgebiet Reaktive Stroemungen und Messtechnik, Center of Smart Interfaces Technische Universitaet Darmstadt, Petersenstrasse 32, 64287 Darmstadt (Germany)

2011-04-15

With regard to phosphor thermometry, seven luminescent ceramic materials were synthesised and characterised, namely CaMoO{sub 4}:Eu{sup 3+}, CaTiO{sub 3}:Pr{sup 3+}, LaPO{sub 4}:Eu{sup 3+}, LaVO{sub 4}:Eu{sup 3+}, LiAl{sub 5}O{sub 8}:Fe{sup 3+}, TiMg{sub 2}O{sub 4}:Mn{sup 4+} and ZnGa{sub 2}O{sub 4}:Mn{sup 2+}. In this context, emission spectra and temperature lifetime characteristics are presented. Thus, a survey of phosphors novel for thermography is given in order to encourage further studies and more detailed characterisations of the respective materials. - Research Highlights: Seven phosphor materials novel for thermometry were synthesised. These materials were characterised diffractometrically as well as concerning their emission spectra and lifetime temperature characteristics. The number of phosphor materials characterised for thermometry purposes was extended by seven materials.

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)

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

Directory of Open Access Journals (Sweden)

Hwangbo Seung

2015-06-01

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

Synthesis, luminescence, and energy-transfer properties of β-Na2Ca4(PO4)2(SiO4):A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors.

Science.gov (United States)

Li, Kai; Shang, Mengmeng; Geng, Dongling; Lian, Hongzhou; Zhang, Yang; Fan, Jian; Lin, Jun

2014-07-07

A series of β-Na2Ca4(PO4)2(SiO4) (β-NCPS):A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors were prepared via a high-temperature solid-state reaction route. The X-ray diffraction, Fourier transform infrared, photoluminescence (PL), cathodoluminescence (CL) properties, fluorescent lifetimes, and absolute quantum yield were exploited to characterize the samples. Under UV radiation, the β-NCPS:Eu(2+) phosphors present bright green emissions, and the β-NCPS:Ce(3+) phosphors show strong blue emissions, which are attributed to their 4f(6)5d(1) → 4f(7) and 5d-4f allowed transitions, respectively. The β-NCPS:Ce(3+), Tb(3+) phosphors display intense tunable color from blue to green and high absolute quantum yields (81% for β-NCPS:0.12Ce(3+) and 83% for β-NCPS:0.12Ce(3+), 0.08Tb(3+)) when excited at 365 nm. Simultaneously, the energy transfer from Ce(3+) to Tb(3+) ions is deduced from the spectral overlap between Ce(3+) emission and Tb(3+) excitation spectra and demonstrated by the change of emission spectra and decay lifetimes. Moreover, the energy-transfer mechanism from Ce(3+) to Tb(3+) ions is confirmed to be exchange interaction according to the discussion of expression from Dexter and Reisfeld. Under a low-voltage electron-beam excitation, the β-NCPS:A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors exhibit their characteristic emissions, and the emission profiles of β-NCPS:Ce(3+),Tb(3+) phosphors are obviously different from those of the PL spectra; this difference might be ascribed to their different luminescence mechanisms. These results in PL and CL properties suggest that β-NCPS:A (A = Eu(2+), Dy(3+), Ce(3+)/Tb(3+)) phosphors are potential candidates for solid-state lighting and field-emission displays.

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.

Study on emission of decomposed chemicals of esters contained in PVC flooring and adhesive

Energy Technology Data Exchange (ETDEWEB)

Chino, Satoko; Ataka, Yuji [R and D Center, Yoshino Gypsum Co., Ltd., 2-1-1 Kohoku, Adachi-ku, Tokyo, 123-0872 (Japan); Kato, Shinsuke; Seo, Janghoo [Institute of Industrial Science, The University of Tokyo, 4-6-1 Komaba, Meguro-ku, Tokyo 153-8505 (Japan)

2009-07-15

2-Ethyl-1-hexanol (2E1H) is sometimes detected in indoor air at relatively high concentrations. The emission mechanism for 2E1H is considered to be that moisture with a high pH in concrete slabs and self-leveling sub-flooring material reacts with di-2-ethylhexyl phthalate (DEHP) in the polyvinyl chloride (PVC) flooring and compounds containing the 2-ethyl-1-hexyl group in the adhesive. 2E1H is considered to be one of the causes of odor in indoor air and sick building syndrome, so it is important to clarify the 2E1H emission mechanism for IAQ. However, there are few reports on any experimentation into 2E1H emission by chemical reaction involving building materials. In this study, PVC floorings are attached using various adhesives to a self-leveling sub-flooring material that contains water, and their 2E1H emission rates are measured. Furthermore, the components of the adhesives are determined using chemical analysis. It is found that 2E1H emission rates from the floor are affected by the type of adhesive used. On the other hand, some components in the adhesives may suppress the hydrolysis of esters. The hydrolysis of polymers and residual monomers in the adhesive causes 2E1H emission from the adhesive. (author)

Luminescence and luminescence quenching of Sr{sub 3}Lu{sub 2}(Si{sub 3}O{sub 9}){sub 2}:Ce{sup 3+} phosphors

Energy Technology Data Exchange (ETDEWEB)

Mikalauskaite, I.; Raudonyte-Svirbutaviciene, E. [Institute of Chemistry, Faculty of Chemistry and Geosciences, Vilnius University, Naugarduko 24, LT-03225 Vilnius (Lithuania); Linkeviciute, A. [State Research Institute, Centre for Physical Sciences and Technology, Sauletekio Avenue 3, LT-10257 Vilnius (Lithuania); Urbonas, M. [Institute of Chemistry, Faculty of Chemistry and Geosciences, Vilnius University, Naugarduko 24, LT-03225 Vilnius (Lithuania); Katelnikovas, A., E-mail: arturas.katelnikovas@chf.vu.lt [Institute of Chemistry, Faculty of Chemistry and Geosciences, Vilnius University, Naugarduko 24, LT-03225 Vilnius (Lithuania)

2017-04-15

A series of near-UV to blue emitting Sr{sub 3}Lu{sub 2}(Si{sub 3}O{sub 9}){sub 2}:Ce{sup 3+} phosphors were prepared by a solid state reaction. The optical properties of synthesized phosphors were investigated as a function of Ce{sup 3+} concentration and temperature. These luminescent materials strongly absorb UV radiation shorter than 360 nm. The optimal Ce{sup 3+} concentration was 0.1% (external quantum efficiency ca. 45%). Temperature dependent measurements showed that Sr{sub 3}Lu{sub 2}(Si{sub 3}O{sub 9}){sub 2}:Ce{sup 3+} phosphors possess good thermal stability and loses only about 40% to 50% of initial intensity in the temperature range of 77–500 K depending on activator concentration.

Preparation and luminescence of green-emitting ZnAl{sub 2}O{sub 4}:Mn{sup 2+} phosphor thin films

Energy Technology Data Exchange (ETDEWEB)

Huang, Ing-Bang [Department of Materials Science and Engineering, National Formosa University, Huwei, Yunlin 632, Taiwan (China); Chang, Yee-Shin [Department of Electronic Engineering, National Formosa University, Huwei, Yunlin 632, Taiwan (China); Chen, Hao-Long [Department of Electronic Engineering, Kao Yuan University, Lujhu, Kaohsiung 821, Taiwan (China); Hwang, Ching Chiang [Department of Biotechnology, Mingdao University, Chang-Hua 52345, Taiwan (China); Jian, Chen-Jhu; Chen, Yu-Shiang [Department of Materials Science and Engineering, National Formosa University, Huwei, Yunlin 632, Taiwan (China); Tsai, Mu-Tsun, E-mail: mttsai@ms23.hinet.net [Department of Materials Science and Engineering, National Formosa University, Huwei, Yunlin 632, Taiwan (China)

2014-11-03

Nanocrystalline Mn{sup 2+}-doped zinc spinel (ZnAl{sub 2}O{sub 4}:Mn{sup 2+}) green-emitting phosphor films were deposited on silicon substrate by sol–gel spin coating and subsequent heat treatment up to 1000 °C. The effects of dopant concentration and heat treatment on the optical and structural properties were investigated. The variations in sol viscosity with time, film thickness with number of layers were also examined. Thin films were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, energy-dispersive X-ray microscopy, atomic force microscopy, and photoluminescence spectrum. Single-phase ZnAl{sub 2}O{sub 4} started to crystallize at around 600 °C, with a normal spinel structure. On annealing at 1000 °C, the films had smooth surfaces with a nanocrystalline structure. Under UV or visible light excitation, the phosphor films exhibited an intense green emission band peaking at around 512 nm, corresponding to the typical {sup 4}T{sub 1} → {sup 6}A{sub 1} transition of tetrahedral Mn{sup 2+} ions. The most intense green emission was obtained by exciting at 456 nm. The emission intensity of films was highly dependent upon the excitation wavelength, crystallinity, dopant content, and deposition conditions. The results show that the ZnAl{sub 2}O{sub 4}:Mn{sup 2+} films have good potential for use as a green phosphor for displays and/or white light-emitting diodes. - Highlights: • ZnAl2O4:Mn2 + thin film phosphors have been synthesized by a sol–gel process. • The most intense green emission was obtained by exciting at 456 nm. • Photoluminescence is highly dependent on the crystallinity and doping content. • Emission intensity can also be modulated by controlling the film thickness.

Ethyl 4-chloro-2′-fluoro-3-hydroxy-5-methylbiphenyl-2-carboxylate

Directory of Open Access Journals (Sweden)

Muhammad Adeel

2011-09-01

Full Text Available In the title compound, C16H14ClFO3, the dihedral angle between the mean planes of the two benzene rings is 71.50 (5°. Due to an intramolecular O—H...O hydrogen bond between the hydroxy group and the carbonyl O atom of the ethyl ester group, the ethyl ester group lies within the ring plane. The crystal structure is consolidated by intermolecular C—H...O and C—H...F interactions.

Synthesis and tunable luminescence properties of Eu2+ and Tb3+-activated Na2Ca4(PO4)3F phosphors based on energy transfer

International Nuclear Information System (INIS)

Zhou, Jun; Xia, Zhiguo; You, Hongpeng; Shen, Kai; Yang, Mengxia; Liao, Libing

2013-01-01

A series of color-tunable blue–green emitting Na 2 Ca 4 (PO 4 ) 3 F:Eu 2+ ,Tb 3+ phosphors were prepared by a high temperature solid-state reaction. Their luminescence properties reveal that there is an efficient energy transfer from Eu 2+ to Tb 3+ ions via a dipole–quadrupole mechanism where Eu 2+ ions exhibit a strong excitation band in near ultraviolet (UV) region, matching well with the dominant emission band of near UV (350–420 nm) LED chips, and Eu 2+ and Tb 3+ ions can give characteristic blue and green emission light. The varied color of the phosphors from blue to green can be achieved by properly tuning the relative ratio of Eu 2+ to Tb 3+ dopant through the energy transfer from Eu 2+ to Tb 3+ ions. Thermal quenching luminescence results reveal that Na 2 Ca 4 (PO 4 ) 3 F:Eu 2+ ,Tb 3+ exhibits good thermal stability. These results demonstrate that Tb 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 Eu 2+ with high oscillator strength. The present Eu 2+ –Tb 3+ codoped Na 2 Ca 4 (PO 4 ) 3 F phosphor will have potential application for the near UV white LEDs. - Highlights: ► Color-tunable blue–green Na 2 Ca 4 (PO 4 ) 3 F:Eu 2+ ,Tb 3+ phosphors were prepared. ► Eu 2+ –Tb 3+ energy transfer process and mechanism discussed. ► Thermal quenching properties of blue and green phosphors were studied.

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.)