SO42-/ZrO2固体超强酸催化剂制备及其催化α-甲基萘异构化性能  被引量:1

Preparation of SO42-/ZrO2 Solid Superacid Catalyst and Its Catalytic Performance in the Isomerization ofα-Methylnaphthalene

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作  者:刘远林[1] 高焕新[1] LIU Yuanlin;GAO Huanxin(State Key Laboratory of Green Chemical Engineering and Industrial Catalysis,Shanghai Research Institute of Petrochemical Technology,SINOPEC,Shanghai 201208,China)

机构地区:[1]中国石油化工集团公司上海石油化工研究院,绿色化工与工业催化重点实验室,上海201208

出  处:《化学反应工程与工艺》2019年第6期570-575,共6页Chemical Reaction Engineering and Technology

基  金:国家重点研发计划(2017YFB0702800)。

摘  要:为了制备性能稳定的高活性α-甲基萘异构化催化剂,对合成的SO42-/ZrO2固体超强酸催化剂进行了多种金属离子掺杂改性。并在固体床反应器中考察了催化剂改性方法、反应温度、反应压力以及空速对改性催化剂催化α-甲基萘异构化反应性能的影响。结果表明,反相共沉淀法并且铝掺杂2%的SO42-/ZrO2固体超强酸催化剂性能最佳,在床层温度230℃,反应压力1.0 MPa,α-甲基萘重时空速(WHSV)为1.0 h^-1的优化反应条件下,原料α-甲基萘转化率大于70%,产物β-甲基萘的选择性大于95%,重组分选择性小于0.2%。催化剂的稳定性和再生实验结果表明催化剂再生性能优良,具有良好的工业应用前景。In order to prepare stable high activity catalyst ofα-methylnaphthalene isomerization,the synthesized SO42-/ZrO2 solid superacid catalyst was modified by metal ion doping.The effects of catalyst modification method,reaction temperature,reaction pressure and weight hourly space velocity(WHSV)on the isomerization ofα-methylnaphthalene were investigated in a fixed bed reactor.The results showed that the performance of SO42-/ZrO2 solid superacid catalyst prepared by reverse dropping method and doped with 2%Al was the best.Under the optimal operating conditions of temperature 230℃,pressure 1.0 MPa and the WHSV ofα-methylnaphthalene 1.0 h^-1,the conversion ofα-methylnaphthalene was more than 70%,the selectivity ofβ-methylnaphthalene was more than 95%and the selectivity of recombinants was less than 0.2%.The experimental results of catalyst stability and regeneration showed that the catalyst regeneration performance was excellent,which has a good prospect of industrial application.

关 键 词:超强酸 甲基萘 异构化 

分 类 号:O643.36[理学—物理化学]

 

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