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Preparation of 1-octene by ethylene tetramerization with high selectivity
作者姓名:JIANG  Tao  CHEN  Hongxia  NING  Yingnan  CHEN  Wei
作者单位:[1]School of Chemistry and Chemical Engineering, Daqing Petroleum Institute, Daqing 163318, China [2]SINOPEC Beijing Research Institute of Chemical Industry, Beijing 100013, China
摘    要:Two novel PNP ligands have been synthesized and characterized by ^1H-NMR, elemental analysis, and mass spectra. In combination with Cr(Ⅲ) and cocatalyst MAO, they generate active catalytic systems that tetramerize ethylene with both high catalytic activity and high selectivity to produce 1-octene. The results show that these catalyst systems are able to catalyze ethylene tetramerization, with high catalytic activity up to 0.89×10^6 g/mol Cr.h, and the selectivity of C8 in products is 72.52%, and the percentage of 1-olefins in the C8 cut is 97.87%.

关 键 词:1-辛烯  制备  乙烯    催化剂  MAO
收稿时间:2005-08-03
修稿时间:2005-08-032005-09-09

Preparation of 1-octene by ethylene tetramerization with high selectivity
JIANG Tao CHEN Hongxia NING Yingnan CHEN Wei.Preparation of 1-octene by ethylene tetramerization with high selectivity[J].Chinese Science Bulletin,2006,51(5):521-523.
Authors:Tao Jiang  Hongxia Chen  Yingnan Ning  Wei Chen
Institution:(1) School of Chemistry and Chemical Engineering, Daqing Petroleum Institute, Daqing, 163318, China;(2) SINOPEC Beijing Research Institute of Chemical Industry, Beijing, 100013, China
Abstract:Two novel PNP ligands have been synthesized and characterized by 1H-NMR, elemental analysis, and mass spectra. In combination with Cr(III) and cocatalyst MAO, they generate active catalytic systems that tetramerize ethylene with both high catalytic activity and high selectivity to produce 1-octene. The results show that these catalyst systems are able to catalyze ethylene tetramerization, with high catalytic activity up to 0.89×106 g/mol Cr.h, and the selectivity of C8 in products is 72.52%, and the percentage of 1-olefins in the C8 cut is 97.87%.
Keywords:ethylene tetramerization  1-octene  Cr(III)  MAO
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