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作 者:Jun Wang Hongpeng Li Xi Chen Weiguang Shi Na Zhang Fuquan Bai Xiaofeng Wang Sihan Wang Xianming Xu Libo Wang
机构地区:[1]Provincial Key Laboratory of Oil and Gas Chemical Technology,College of Chemistry and Chemical Engineering,Northeast Petroleum University,Daqing 163318,China [2]Daqing Chemical Research Center of Petrochemical Research Institute,Daqing 163714,China [3]Institute of Theoretical Chemistry,Jilin University,Changchun 130023,China [4]State Key Laboratory of Inorganic Synthesis and Preparative Chemistry,College of Chemistry,Jilin University,Changchun 130012,China
出 处:《Chinese Journal of Chemical Engineering》2019年第11期2687-2695,共9页中国化学工程学报(英文版)
基 金:Support by National Key Research and Development Program of China(2017YFB0306701);State Key Laboratory Opening Project Foundation of Jilin University(2018-16).
摘 要:The BF3/n-BuOH complexes were investigated as active species in catalyzing n-decene polymerization reaction.The structures of BF3/n-BuOH complexes were characterized not only by modern spectrum but also by calculation at theoretical level. The results confirmed that BF3/n-BuOH complexes changed from BF3·(n-BuOH)2 complexes to BF3·n-BuOH complexes with the mass fraction of BF3 increasing. These two complexes have different catalytic activity, but BF3·n-BuOH was superior. The highest n-decene conversion could reach 99% and the most excellent selectivity of n-decene trimer and tetramer could reach up to 80% yield by a series of controlled conditions. This work can help to understand the catalytic active species of n-decene polymerization and provide support for industrialization of poly-alpha-olefins(PAOs).The BF3/n-Bu OH complexes were investigated as active species in catalyzing n-decene polymerization reaction.The structures of BF3/n-Bu OH complexes were characterized not only by modern spectrum but also by calculation at theoretical level. The results confirmed that BF3/n-Bu OH complexes changed from BF3·(n-Bu OH)2 complexes to BF3·n-Bu OH complexes with the mass fraction of BF3 increasing. These two complexes have different catalytic activity, but BF3·n-Bu OH was superior. The highest n-decene conversion could reach 99% and the most excellent selectivity of n-decene trimer and tetramer could reach up to 80% yield by a series of controlled conditions. This work can help to understand the catalytic active species of n-decene polymerization and provide support for industrialization of poly-alpha-olefins(PAOs).
关 键 词:BORON TRIFLUORIDE n-BuOH n-decene POLYMERIZATION Catalyst structures
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