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1.
The green phosphor for white LED, Ca8Mg(SiO4)4Cl2∶Eu2+, Mn2+, was synthesized by high temperature solid state reaction under reducing atmosphere. During the process of the phosphor prepared, the excess CaCl2 can improve the intensity of emission. The experimental results indicate that there is an effective energy transfer from Eu2+ to Mn2+in Ca8Mg(SiO4)4Cl2 host. This kind of energy transfer may be due to resonance transfer, and this energy transfer is limited. 相似文献
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Novel precipitant prepared through carbonation with MgCl2 wastewater generated from rare earth extraction separation process and low-price dolomite as raw materials was studied in this paper. The purification methods of novel precipitant by adding appropriate oxidizing agent were studied. It was found that optimal purification result could be achieved with sodium hypochlorite as iron removal reagent and the iron removal rate could reach up to 90% when the adding amount was 0.1 vol.%. During the preparation, the particle size and distribution of ceria-based polishing powder were affected obviously by the parameters such as concentration, reaction temperature and feeding rate. The results showed that ceria-based polishing powder with D50 =2.5-3.5 μm and the particle size distribution of 0.65-0.75 μm could be prepared when the concentration of CeCl3 was 0.6 mol/L, the reaction temperature was maintained at 50 °C and the feeding speed was controlled at 25 ml/min. Compared with commercial powder, the self-made polishing powder had roughly the same cutting amount, but the surface finish of polished glass was better than that of commercial polishing powder. 相似文献
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钙钛矿催化材料La1-xCexCoO3+δ的制备、表征及甲烷燃烧催化性质 总被引:5,自引:2,他引:5
采用柠檬酸发泡法制备了钙钛矿LaCoO3催化材料;研究了Ce对La进行掺杂替代对催化材料性能的影响;通过BET、XRD、SEM等手段对催化材料进行了物性表征;以甲烷完全燃烧为目标反应,研究了钙钛矿La1-xCexCoO3 δ的催化性能.结果表明:铈掺杂对材料晶相有较大影响,当掺杂量x小于0.3时,粉体晶型基本不变,而当掺杂量达到0.5时,有明显CO3O4晶相出现,LaCoO3钙钛矿晶相完整性遭到破坏,当掺杂量大于0.7时,钙钛矿晶相大大弱化甚至消失;LaCoO3是一种性能优良的甲烷燃烧催化材料,Ce的掺杂替代对催化材料活性有明显影响,并增强了催化材料的高温稳定性能,铈最佳掺杂量为0.3;前驱体经700℃焙烧形成了较为完整的钙钛矿晶型,经800℃焙烧后,催化材料最高活性为:t10%=390℃,t90%=603℃. 相似文献
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Spherical (Y, Gd)BO3:Eu^3+ phosphor particles with a narrow size distribution(2 -4 μm) was obtained by firing the Y-Gd-Eu-BO3 precursor prepared in a W/O style emulsion system. In the W/O emulsion system, kerosene, used as oil phase, was mixed with Span 80 and Tween 80 compounds which were employed as the emulsifier with an HLB (hydrophile-lipophile balance) value of 5.2- 5.3. Both rare earths (Y, Gd and Eu) nitrate and boric acid solution or ammonia solution were used as aqueous phase. The synthesis conditions, such as emulsion composition, emulsifying style, precipitation reaction process, reaction temperature, morphology control, and so on, were investigated, and the optimum synthesis conditions for preparing spherical (Y, Gd)BO3:Eu^3+ phosphor was obtained. The phosphor was characterized by XRD, SEM, laser particle size analysis, emission and excitation spectrum under vacuum ultraviolet (VUV), and so on. The phosphor synthesized using the water-in-oil emulsion method with median diameter (D50) of 2 - 4 μm shows agreeable photoluminescence (PL) property and sphericity. The main emission peak appears at about 593 nm, which corresponds to ^5D0→^7F1 transition (magnetic-dipole transition) of the Eu^3+ ion. The cell parameters and powder diffraction data were indexed. The structure of the phosphor belongs to the hexagonal system with space group P63/m. 相似文献
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High calcination temperature is an important factor in the preparation process of CeMgAl11O19:Tb^3 . To decrease the temperature, different fluxes (H3BO3, MgF2 and AlF3) were tested in order to compare their influence on the luminescence property and particle size distribution of CeMgAl11O19: Tb^3 . The result shows that when the content of MgF2 is 0.1 mol/mol, the intensity of luminescence can attain a maximum. Furthermore, MgF2 can improve the particle size quality of the phosphor. So MgF2 can take the place of the conventional flux H3BO3 to prepare high quality CeMgAl11O19:Tb^3 phosphor. In addition, the relation between phosphor property and content of AlF3 was also studied. The crystal structure of the phosphor was analyzed by XRD method. The phase composition analysis shows that the reason of decrease of the brightness of CeMgAl11O19:Tb^3 phosphor is the emergence of TbAlO3 and α-Al2O3 during the preparation process. 相似文献
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(Y,Gd)BO3∶ Eu phosphors were prepared by co-precipitation precursors, and luminescent properties were investigated. The precursors were synthesized by introducing hydroxyl ion to mixed solution of rare earth nitrates and boric acid, either through adding ammonia(precursor 1)or through controlled release of hydroxyl ion of urea(precursor 2). The precursors were fired in air at 1000 ℃ for 2 h. Resulted phosphor synthesized with precursor 1 has non-uniformed particle with mean diameter of about 3 μm, while that with precursor 2 exhibits uniformed near spherical-like morphology with mean diameter of about 300 nm. Phosphors with the two methods exhibit same crystal structure as that of commercial one. Emission spectra of the samples indicate that the sample prepared with precursor 2 shows relative higher intensity(exited by 172 nm VUV)than that prepared with the other precursor. 相似文献
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