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作 者:魏昭彬[1] 辛勤[1] 盛世善 陈恒荣[1] 刘敬利[1] 蒋建明[1]
机构地区:[1]中国科学院大连化学物理研究所催化基础国家重点实验室,化工部天津化工研究院
出 处:《Chinese Journal of Catalysis》1994年第4期243-249,共7页催化学报(英文)
摘 要:本文考察了CoMo/TiO3和CoMo/γ-Al2O3催化剂的加氢脱硫性能及表面结构变化和预处理条件对其活性的影响.担体TiO2(A)和TiO2(B)分别采用TiCl4中和法和TiOSO4水解法制备.结果表明,催化剂的活性顺序为CoMo/TiO2(A)>CoMo/TiO2(B)>CoMo/γ-Al2O3催化剂的预处理条件对催化剂的加氢脱硫(HDS)和加氢(HYD)活性有很大影响,TiO2担体上Mo物种主要以八面体配位构型存在,Mo6+更易于还原成低价态.ydrodesulfurization activity of CoMo/TiO2 and CoMo/γ-Al2O3catalysts was examined by using a microreactor operating at 3. 0 MPaH2pressure.The surface structure and reducibility in H2 at 450℃ of these catalysts were characterized by LRS and XPS. For CoMo/TiO2 catalysts, TiO2 carrier was prepared by two methods:TiO2(A) was prepared by using ammonium water neutralizing TiCl4 solution, while TiO2 (B) was prepared by the hydrolysis of TiOSO4 Before the measurement of thiophene HDS and cyclohexene HYD, the catalysts were pretreated by sulfiding or reducing or without any treatment.The results obtained are: (1) The HDS and HYD activities of CoMo/TiO2 (A) and CoMo/TiO2(B) catalysts are much higher than that of CoMo/γ-Al2O3 catalyst.The obvious influence of preparation technology of TiO2 carrier on the CoMo/TiO2 catalyst can be observed.(2) Pretreating conditions obviously influence the HDS and HYD activities of CoMo/TiO2 (A),(B)and CoMo/γ-Al2O3. The best way is presulfiding treatment in H2-H2S at 400℃ For CoMo/TiO2 catalyst without any pretreatment relatively high activity is exhibited, which is of significance in terms of industrial application. (3) The surface structure of CoMo/TiO2 catalyslts is differeht from CoMo/γ-Al2O3. LRS spectra show that the strong band of bridged Mo-O-Mo species existed in CoMo/TiO2 (A), XPS results demonstrate that more Mo6+ species of CoMo/TiO2 than that of CoMo/γ-Al2O3 can be reduced to Mo4 + ions, which. reveals that TiO2 carrier can favor the reduction of Mo6+ species.
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