稀有金属
稀有金屬
희유금속
CHINESE JOURNAL OF RARE METALS
2010年
1期
58-62
,共5页
余倩%余林%张绮旎%孙明%凌伟军%许奕祥
餘倩%餘林%張綺旎%孫明%凌偉軍%許奕祥
여천%여림%장기니%손명%릉위군%허혁상
二甲醚%热分解动力学%六铝酸盐%催化剂
二甲醚%熱分解動力學%六鋁痠鹽%催化劑
이갑미%열분해동역학%륙려산염%최화제
dimethyl ether%thermal decomposition kinetics%hexaaluminate%catalyst
采用反相微乳法制备和超临界干燥获得前驱体BaO·MnO·6Al_2O_3.利用TG-DTA曲线和XRD分析对前驱体的热分解过程进行研究,并用Coats-Redfem法和Kissinger法进一步研究前驱体的热分解动力学,获得六铝酸盐催化剂前驱体热分解的机制函数为:积分式G(α)=[-ln(1-α)]~4,微分式为:f(α)=(1/4)(1-α)[-ln(1-α)]~(-3),反应为随机成核和随后生长控制,计算出的活化能E_a=187.80 kJ·mol~(-1).
採用反相微乳法製備和超臨界榦燥穫得前驅體BaO·MnO·6Al_2O_3.利用TG-DTA麯線和XRD分析對前驅體的熱分解過程進行研究,併用Coats-Redfem法和Kissinger法進一步研究前驅體的熱分解動力學,穫得六鋁痠鹽催化劑前驅體熱分解的機製函數為:積分式G(α)=[-ln(1-α)]~4,微分式為:f(α)=(1/4)(1-α)[-ln(1-α)]~(-3),反應為隨機成覈和隨後生長控製,計算齣的活化能E_a=187.80 kJ·mol~(-1).
채용반상미유법제비화초림계간조획득전구체BaO·MnO·6Al_2O_3.이용TG-DTA곡선화XRD분석대전구체적열분해과정진행연구,병용Coats-Redfem법화Kissinger법진일보연구전구체적열분해동역학,획득륙려산염최화제전구체열분해적궤제함수위:적분식G(α)=[-ln(1-α)]~4,미분식위:f(α)=(1/4)(1-α)[-ln(1-α)]~(-3),반응위수궤성핵화수후생장공제,계산출적활화능E_a=187.80 kJ·mol~(-1).
The precursor BaO·MnO·6Al_2O_3 of catalyst BaMnAl_(11)O_(19-δ )was prepared by reverse microemulsion method and dried by supercritical drying.The thermal decomposition process of the precursor was studied with TG-DTA and XRD.And the thermal decomposition kinetics of the precursor was studied with Coats-Redfem methed and Kissinger method.According to the calculation results of Kissinger method and Coats-Redfem method,the thermal decomposition mechanism function of the precursor could be described as integral form G(α)=[-ln(1-α)]~4 and differential form f(α)=(1/4)(1-α)[-ln(1-α)]~(-3).The thermal decomposition reaction of the precursor was followed with the mechanism of random nucleation and subsequent growth.And the activation energy was187.80kJ·mol_(-1).