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31.
Mechanochemical Reaction of Lanthanum Carbonate with Sodium Hydroxide and Preparation of Lanthanum Oxide Nanoparticle 总被引:3,自引:0,他引:3
Theimportanceofnanosizedrareearthoxidepowdersinvarioustechnicalapplicationsmakestheirpreparationtechnologyaninterest ingsubjectforresearchwork[1 ] .Overthepastdecades,manypreparationmethodsofnano sizedrareearthoxideshavebeendeveloped ,includingphysicaland… 相似文献
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单分散球形超细氧化铈的机械化学反应制备法 总被引:10,自引:0,他引:10
采用湿固相机械化学反应法制备单分散球形超细氧化铈粉体,化学分析和XRD物相分析结果表明球磨作用不仅改善了反应的热力学和动力学条件,使反应能在较短的时间内完成,而且还促进了产物的结晶化,得到了结晶性良好的新物相,有利于球磨产物的后续处理。随着球磨反应的进行,颗粒粒度减小,直至亚微米级时球磨反应使颗粒的减小趋势与晶粒生长导致颗粒长大的趋势达到平衡,粒度降低幅度减小。球磨产物在后续煅烧过程中,其粒度随温度的升高是先减小而后增大,但在1050℃之前的增大不够明显。XRD、粒度分布及扫描电镜分析结果表明煅烧产物为球形的单分散的超细氧化铈。 相似文献
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YAG: Ce^3 + phosphor particles were prepared using polyacrylamide gel method. The structure evolution of powders during annealing process was followed by X-ray diffraction determination. It is found that some intermediate phases, including θ-Al2O3, YAM and YAP, are formed when calcining polyacrylamide gel, however, the pure YAG phase can be formed directly when calcining polyacrylamide gel with α-Al2O3 as seed crystal. These facts show that the existence of α- Al2O3 seed crystal can block the formation of θ-Al2O3, YAM and YAP, and accelerate its reaction with Y2O3 to form YAG phase directly at lower temperature. The emission peak of prepared YAG : Ce^3 + phosphor is wide with maximum at 550 nm and the exitation band has two peaks, the major one is around at 460 nm, which matches the blue emission of GaN LED and is suitable for the assemble of white LED. Some fluxes can enhance the photoluminescence intensity of phosphor particles, that can be attributed both to the improvement of crystallization processes of YAG and to the stabilization of trivalence cerium ion in YAG:Ce^3 +. 相似文献
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湿固相机械化学法制备蓝粉前驱体过程中的物相转变 总被引:4,自引:0,他引:4
采用湿固相机械化学法制备稀土铝酸盐蓝色荧光粉前驱体,用XRD和DTA-TG分析技术研究了湿固相球磨过程和后续煅烧过程中的物相转变。结果表明:在球磨过程中反应原料经历了无定型化与水热结晶两个主要阶段,观察到了MgAl2O4尖晶石结构相的形成和BaMg(CO3)2及BaCO3的再结晶现象,这些晶相在640℃之前仍保持稳定。在烧成过程,首先发生无定型Al(OH)3的分解,而后是分两个阶段的BaMg(CO3)2和BaCO3分解过程,到900℃时,碳酸盐的分解才基本结束,但没有形成高温固相反应所得到的BaMgAl10O16晶相。扫描电镜观察和粒度分析结果表明所得前驱体为粒度1-3μm,分散性良好的亚球形蓝色荧光粉前驱体。 相似文献
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Nano-sized yttria particles were synthesized via a non-aqueous sol-gel process based on hydrated yttrium nitrate and ethylene glycol. The effects of the molar ratio of ethylene glycol to yttrium ion and calcination temperature on crystallite size of the products were studied. The catalytic performance of the as-prepared yttria for the ammonium perchlorate (AP) decomposition was investigated by differential scanning calorimetry (DSC). The results indicate that the nano-sized cubic yttria particles with less than 20 nm in average crystallite size can be obtained after 2 h reflux at 70 ℃, dried at 90 ℃, forming xerogel, and followed by annealing of xerogel for 2 h, and that the addition of the nano-sized yttria to AP incorporates two small exothermic peaks of AP in the temperature ranges of 310 ~ 350 ℃ and 400 ~ 470 ℃ into a strong exothermic peak of AP and increases the apparent decomposition heat from 515 to over 1110 J·g-1. It is also clear that the temperature of AP decomposition exothermic peak decreases and the apparent decomposition heat of AP increases with the increase of the amount of nano-sized yttria. The fact that the addition of the 5 % nano-sized yttria to AP decreases the temperature of AP exothermic peak to 337.7 ℃ by reduction of 114.6 ℃ and increases the apparent decomposition heat from 515 to 1240 J·g-1, reveals that nano-sized yttria shows strong catalytic property for AP thermal decomposition. 相似文献
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