氧化铝-氧化锆复合载体制备碳二前加氢催化剂的性能评价  被引量:4

Performance evaluation of C_2 front-end hydrogenation catalyst supported on Al_2O_3-ZrO_2 composite carrier

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作  者:韩伟 赵玉龙 任世宏 车春霞 梁玉龙 钱颖 谭都平 

机构地区:[1]中国石油兰州化工研究中心,甘肃兰州730060 [2]中国石油大庆石化公司,黑龙江大庆163001

出  处:《石化技术与应用》2015年第2期122-124,132,共4页Petrochemical Technology & Application

基  金:中国石油天然气股份有限公司资助项目(项目编号:2013 B-2608)

摘  要:利用氧化铝(Al2O3)-氧化锆(Zr O2)复合载体,采用等体积分布浸渍法制备碳二(C2)前加氢催化剂,对其孔结构及表面酸性进行了表征,并在实验室100 m L C2加氢反应器上评价其加氢性能。结果表明,所制备催化剂呈特定双峰孔径分布,孔径分布在80~150 nm,160~400 nm,相应的最可几孔径分别为110,280 nm;表面总酸量为22.023 mmol/g;在反应器入口温度为68℃的条件下运行500 h,与同类型进口催化剂相比,所制备催化剂床层温升降低了4℃,乙炔转化率、乙烯选择性、丙炔及丙二烯(MAPD)转化率分别高出4.2,2.0,1.0个百分点,MAPD选择性降低了2.0个百分点,绿油及焦炭生成量均较低。Using alumina ( Al2O3 ) - zirconia ( ZrO2 ) composite carrier, the C2 front - end hydrogenation catalyst was prepared by isovolume impregnation method. The pore structure and surface acidity of the catalyst were characterized, and the hydrogenation performance of the catalyst was evaluated in a 100 mL C2 hydrogenation reactor. The results showed that the home -made catalyst had the characteristics of bimodal pore size distribution, which ranged between 80 - 150 nm and 160 - 400 nm, and their most probable pore sizes were 110 nm and 280 nm respectively;the total acidity of the catalysts was 22. 023 mmol/g Through operating at 68 ℃ of inlet temperature for 500 h, compared to the same type of imported catalysts,the bed temperature rise of the home - made catalyst decreased by 4 ℃ , the conversion of acetylene, the selectivity of ethylene, and the conversion of propyne plus propadiene ( MAPD ) increased by 4.2,2. 0 and 1.0 percent points respectively, the selectivity of MAPD decreased by 2.0 percent points, and the yields of green oil and coke were lower.

关 键 词:加氢催化剂 碳二前加氢 氧化铝 氧化锆 载体 孔结构 表面酸性 加氢性能 

分 类 号:TE624.95[石油与天然气工程—油气加工工程]

 

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