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Preparation of nano-sized lutetium aluminum garnet powders using ammonia hydrogen carbonate as precipitant

机译:使用氨碳酸氢盐作为沉淀剂的纳米型铝石榴石粉末的制备

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Nano-sized lutetium aluminum garnet (Lu_3Al_5O_(12), LuAG) powder was co-precipitated from a mixed solution of aluminum and lutetium nitrates using ammonia hydrogen carbonate (AHC) as precipitant. The component, phase evolution and thermal decomposition of the precursor during calcination were studied by FTIR, XRD and TG-DSC. The particle size and morphology of the synthesized powders were determined by TEM. It was found that the precursor was amorphous carbonate and transformed to pure LuAG phase after being calcined at 900 °C for 2 h. LuAG crystallite grew with increasing calcined temperature. The crystallization stage was characterized by an exothermic peak of DSC curve at 1064 °C. This temperature was higher than that detected by XRD, which was caused by the difference in soaking time and the hysteresis of the TG-DSC analyzer. The resultant LuAG powders were loosely agglomerated with an average particle size 50nm. However, the addition of small amount of hydroxypropyl cellulose (HPC) as dispersant can reduce the agglomeration and particle size of the produced LuAG powders. The size of LuAG powder is about 30nm in the presence of HPC.
机译:纳米大小的铝石榴石(Lu_3Al_5O_(12),Luag)粉末从铝和硝酸盐的混合溶液中共沉淀,氨碳酸氢盐(AHC)作为沉淀剂。通过FTIR,XRD和TG-DSC研究了煅烧过程中前体的组分,相位蒸变和热分解。通过TEM测定合成粉末的粒度和形态。结果发现前体是无定形碳酸盐,并在900℃下煅烧2小时后转化为纯Luag相。 Luag Crystallite随着煅烧温度的增加而增长。结晶阶段的特征在于DSC曲线在1064℃下的放热峰。该温度高于XRD检测的温度,这是由TG-DSC分析仪的浸泡时间和滞后引起的。所得Luag粉末松散地凝聚,平均粒度为50nm。然而,添加少量的羟丙基纤维素(HPC)作为分散剂可以降低所产生的Luag粉末的聚集和粒度。在HPC存在下,Luag粉末的尺寸约为30nm。

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