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作 者:廖森[1] 种丽娜[1] 柴倩[1] 刘刚[1] 陈智鹏[1] 吴文伟[1]
出 处:《广西科学》2010年第4期349-352,共4页Guangxi Sciences
基 金:广西科学基金项目(桂科自0991108;桂科自0832111)资助
摘 要:以CoCl2.6H2O和(NH4)3PO4.3H2O为原料,在适量表面活性剂聚乙二醇-400的存在下,先在室温下研磨反应混合物进行固相反应,然后将反应混合物在80℃下保温陈化4h,接着用水洗去混合物中可溶性的无机盐,然后在110℃下烘干2h,得到(NH4)3CoPO4.H2O晶体材料。用XRD,IR,SEM及TG/DTA对产物进行表征。采用热重差热法(TG/DTA)分析研究该产物的热分解过程。结果表明,(NH4)3CoPO4.H2O在105~800℃有2个显著的失重平台,这2个失重过程机理函数所对应的活化能、频率因子(LnA)及热分解机理机理函数分别为:(a)E=97.83kJ/mol,lnA=23.26s-1,[ln(1-a)];(b)E=87.36kJ/mol,lnA=15.60s-1,1-(1-a)1/2。The crystalline (NH4)3COPO4 · H2O was prepared in the presence of surfactant PEG -400 with fully grinding COCl2 · 6H2O and (NH4)3PO4 · 3H2O as raw materials by a solidstate at room temperature. The reaction mixtures were aged at 80℃ for 4h, then washed with water to remove soluble inorganic salts and dried at 110℃ for 2h to obtain the crystals of (NH4)3CoPO4 · H2O. The products were characterized with XRD, IR,SEM and TG/DTA. The thermal decomposition kinetics of α-LiZnPO4 · H2O was studied by thermo-gravimetric- differential thermal analysis(TG-DTA). The results showed that the thermal decomposition of the (NH4)3CoPO4 · H2O was carred in two well-defined weight loss processes. The activa- tionenergy(E),frequency factor(lnA) and mechanism function[g(α)]for the two processes are: (a) E= 97. 83kJ/mol,lnA =23. 26 s^-1,[-ln(1-a)];(b)E=87.36kJ/mol,lnA =15.60 s^-1,1- (1-a)^1/2 .
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