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Zr(OH)4的晶化对Pt/WO3-ZrO2异构化反应性能的影响
引用本文:康承琳,宋月芹,刘锋,周晓龙,李承烈. Zr(OH)4的晶化对Pt/WO3-ZrO2异构化反应性能的影响[J]. 石油学报(石油加工), 2009, 25(5): 661-666
作者姓名:康承琳  宋月芹  刘锋  周晓龙  李承烈
作者单位:华东理工大学 石油加工研究所, 上海 200237
基金项目:国家重大基础研究"973"项目 
摘    要:采用浸渍法制备了Pt/WO3-ZrO2催化剂,考察了Zr(OH)4的晶化对Pt/WO3-ZrO2催化剂上正己烷异构化性能的影响。结果表明,Zr(OH)4母体的晶化对Pt/WO3-ZrO2的酸性和正己烷异构化性能的影响依赖于负载W后样品的焙烧温度。Zr(OH)4的晶化导致了Zrθ1-W700(θ1为Zr(OH)4母体在空气中的晶化温度,700为负载W后的焙烧温度)上酸中心和Pt/Zrθ1-W700的异构化活性的明显下降,而Zrθ1-W800上的酸中心和Pt/Zrθ1-W700的异构化活性无明显变化。正己烷异构化活性不但与WO3-ZrO2上的其酸性有关,且与其中大量四方相ZrO2的存在密切相关。

关 键 词:水合氧化锆  晶化    氧化钨-氧化锆  异构化  正己烷  
收稿时间:2008-09-01
修稿时间:2008-10-30

EFFECTS OF CRYSTALLIZATION OF ZIRCONIUM HYDROXIDE ON THE ISOMERIZATION PERFORMANCES OF Pt/WO3-ZrO2
Kang Cheng-lin,SONG Yue-Qin,LIU Feng,Zhou Xiao-long,Li Cheng-lie. EFFECTS OF CRYSTALLIZATION OF ZIRCONIUM HYDROXIDE ON THE ISOMERIZATION PERFORMANCES OF Pt/WO3-ZrO2[J]. Acta Petrolei Sinica (Petroleum Processing Section), 2009, 25(5): 661-666
Authors:Kang Cheng-lin  SONG Yue-Qin  LIU Feng  Zhou Xiao-long  Li Cheng-lie
Affiliation:Petroleum Processing Research Center, East China University of Science and Technology, Shanghai 200237, China
Abstract:Pt/WO3-ZrO2 catalysts were prepared by impregnating method. The effect of Zr(OH)4 crystallization on the isomerization performance of Pt/WO3-ZrO2 was investigated. The results showed that the effects of the crystallization of Zr(OH)4 on the acidity of WO3-ZrO2 and the isomerization activity of Pt/WO3-ZrO2 was dependent on the calcination temperature of Zr(OH)4 loaded with W. The crystallization of Zr(OH)4 led to a significant decrease in the acid sites on Zrθ1-W700 and the isomerization activity of Pt/Zrθ1-W700 (θ1 and 700 represented the crystallization temperature of Zr(OH)4. However, the crystallization could not result in the great change in the acid sites on Zrθ1-W800 and the isomerization activity of Pt/Zrθ1-W800. The isomerization activity of the catalyst of Pt/WO3-ZrO2 was related not only to the acidity of WO3-ZrO2, but to the amount of tetragonal zirconia in Pt/WO3-ZrO2.
Keywords:WO3-ZrO2
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