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碳二前脱丙烷前加氢催化剂工艺条件试验
引用本文:韩伟,苟尕莲,冯琪,车春霞,梁玉龙,张峰,钱颖,李海军.碳二前脱丙烷前加氢催化剂工艺条件试验[J].工业催化,2016,24(5):67-69.
作者姓名:韩伟  苟尕莲  冯琪  车春霞  梁玉龙  张峰  钱颖  李海军
作者单位:1.中国石油石油化工研究院兰州中心,甘肃 兰州 730060; 2.中国石油石油化工研究院,北京 102206;; 3.中国石油大庆石化公司,黑龙江 大庆 163714
摘    要:采用浸渍法制备Pd-Ag/α-Al2O3催化剂,采用碳二前脱丙烷前加氢工艺系统考察反应器入口温度、空速和反应压力对催化剂性能的影响。结果表明,随着反应器入口温度升高,乙炔和丙炔+丙二烯转化率提高,乙烯选择性提高至一定值后趋于稳定,丙烯选择性波动不大,正丁烯生成量增加,较为适宜的反应器入口温度为(60~70)℃;随着空速升高,乙炔和丙炔+丙二烯转化率降低,乙烯选择性提高,丙烯选择性变化不大,正丁烯生成量降低,较为适宜的空速为(12 000~14 000)h-1;随着反应压力升高,乙炔转化率和丙炔+丙二烯转化率略增,乙烯选择性降低,较为适宜的反应压力为3.6 MPa。

关 键 词:石油化学工程  前加氢  前脱丙烷  Pd-Ag/&alpha  -Al2O3催化剂  

Process condition tests of C2 front-end hydrogenation catalyst for front-end depropanization process
Han Wei,Gou Galian,Feng Qi,Che Chunxia,Liang Yulong,Zhang Feng,Qian Ying,Li Haijun.Process condition tests of C2 front-end hydrogenation catalyst for front-end depropanization process[J].Industrial Catalysis,2016,24(5):67-69.
Authors:Han Wei  Gou Galian  Feng Qi  Che Chunxia  Liang Yulong  Zhang Feng  Qian Ying  Li Haijun
Affiliation:1.Lanzhou Chemical Industry Research Center of PetroChina, Lanzhou 730060, Gansu, China; 2.Petrochemical Research Institute of PetroChina, Beijing 102206, China; 3.Daqing Petrochemical Company of PetroChina, Daqing 163714, Heilongjiang, China
Abstract:Pd-Ag/α-Al2O3 catalysts were prepared by the impregnation method.The effects of reactor inlet temperatures,reaction pressure and space velocity on the catalytic performance of Pd-Ag/α-Al2O3 catalysts were systematically investigated by C2 front-end hydrogenation in front-end depropanization process.The results showed that with the increase of reactor inlet temperature,the conversion rates of acetylene and (propyne+propadiene) increased,the selectivity to ethylene increased to a certain value and then tended to be stable,the selectivity to propylene had little fluctuation,and n-butene production increased,so the appropriate reactor inlet temperature was (60-70) ℃;with the increase of space velocity,the conversion rates of acetylene and (propyne+propadiene) decreased,the selectivity to ethylene increased,the selectivity to propylene had no change,and n-butene production decreased,so the suitable space velocity was (12 000-14 000) h-1;with the increase of reaction pressure,the conversion rates of acetylene and (propyne+propadiene) enhanced slightly,the selectivity to ethylene declined,and therefore the suitable reaction pressure was 3.6 MPa.
Keywords:petrochemical engineering  front-end hydrogenation  front-end depropanization  Pd-Ag/α-Al2O3 catalyst  
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