中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Effect of reaction engineering factors on biphasic hydroformylation of 1-dodecene catalyzed by water-soluble rhodium complex

文献类型:期刊论文

作者Yang, C; Bi, XY; Mao, ZS
刊名JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
出版日期2002-09-09
卷号187期号:1页码:35-46
关键词1-dodecene biphasic hydroformylation kinetics reaction engineering surfactant
ISSN号1381-1169
其他题名J. Mol. Catal. A-Chem.
中文摘要Hydroformylation of 1-dodecenc in a biphasic system using water-soluble rhodium catalyst RhCl(CO)(TPPTS)(2) [TPPTS: tri(sodium-m-sulfonatophenyl) phosphine] was investigated. The cationic surfactant cetyltrimethyl ammonium bromide (CTAB) was used to enhance the reaction rate of long chain olefin and the ratio of normal/isomeric aldehyde. Experiments were carried out semi-batchwise in a 500 ml Stirred autoclave at 100 degreesC and 1.1 MPa. An orthogonal experimental design was adopted for analyzing the effects of agitation intensity, 1-dodecene concentration, surfactant concentration and organic/water volume ratio on the macro-kinetics and regioselectivity. Several agitation configurations for improving the mixing, dispersion and interphase mass transfer of this 'gas-liquid-liquid reaction system were tested and higher hydroformylation rate and regioselectivity were achieved. The relationship between the extent of emulsification of reaction mixture and the performance of hydroformylation reaction was also studied. Empirical macro-kinetic equations for the initial rate and the correlation of normal/isomeric aldehyde ratio are proposed, which represented the experimental data reasonably well. (C) 2002 Elsevier Science B.V. All rights reserved.
英文摘要Hydroformylation of 1-dodecenc in a biphasic system using water-soluble rhodium catalyst RhCl(CO)(TPPTS)(2) [TPPTS: tri(sodium-m-sulfonatophenyl) phosphine] was investigated. The cationic surfactant cetyltrimethyl ammonium bromide (CTAB) was used to enhance the reaction rate of long chain olefin and the ratio of normal/isomeric aldehyde. Experiments were carried out semi-batchwise in a 500 ml Stirred autoclave at 100 degreesC and 1.1 MPa. An orthogonal experimental design was adopted for analyzing the effects of agitation intensity, 1-dodecene concentration, surfactant concentration and organic/water volume ratio on the macro-kinetics and regioselectivity. Several agitation configurations for improving the mixing, dispersion and interphase mass transfer of this 'gas-liquid-liquid reaction system were tested and higher hydroformylation rate and regioselectivity were achieved. The relationship between the extent of emulsification of reaction mixture and the performance of hydroformylation reaction was also studied. Empirical macro-kinetic equations for the initial rate and the correlation of normal/isomeric aldehyde ratio are proposed, which represented the experimental data reasonably well. (C) 2002 Elsevier Science B.V. All rights reserved.
WOS标题词Science & Technology ; Physical Sciences
类目[WOS]Chemistry, Physical
研究领域[WOS]Chemistry
关键词[WOS]2-PHASE HYDROFORMYLATION ; INTERFACIAL CATALYSIS ; HEAVY ALKENES ; LIGANDS ; SELECTIVITY ; KINETICS ; 1-OCTENE ; SYSTEMS ; ENHANCEMENT ; OLEFINS
收录类别SCI
原文出处://WOS:000177841900003
语种英语
WOS记录号WOS:000177841900003
公开日期2013-11-12
版本出版稿
源URL[http://ir.ipe.ac.cn/handle/122111/5661]  
专题过程工程研究所_研究所(批量导入)
作者单位Chinese Acad Sci, Inst Proc Engn, Beijing 100080, Peoples R China
推荐引用方式
GB/T 7714
Yang, C,Bi, XY,Mao, ZS. Effect of reaction engineering factors on biphasic hydroformylation of 1-dodecene catalyzed by water-soluble rhodium complex[J]. JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL,2002,187(1):35-46.
APA Yang, C,Bi, XY,&Mao, ZS.(2002).Effect of reaction engineering factors on biphasic hydroformylation of 1-dodecene catalyzed by water-soluble rhodium complex.JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL,187(1),35-46.
MLA Yang, C,et al."Effect of reaction engineering factors on biphasic hydroformylation of 1-dodecene catalyzed by water-soluble rhodium complex".JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL 187.1(2002):35-46.

入库方式: OAI收割

来源:过程工程研究所

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