Macro-kinetics of biphasic hydroformylation of 1-dodecene catalyzed by water-soluble rhodium complex
文献类型:期刊论文
作者 | Zhang, YQ; Mao, ZS; Chen, TY |
刊名 | CATALYSIS TODAY
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出版日期 | 2002-05-15 |
卷号 | 74期号:1-2页码:23-35 |
关键词 | 1-dodecene hydroformylation gas-liquid-liquid system reaction engineering kinetics surfactant |
ISSN号 | 0920-5861 |
其他题名 | Catal. Today |
中文摘要 | Hydroformylation of 1-dodecene was studied in a biphasic system using water-soluble rhodium complex, RhCl(CO) (TPPTS)(2) (TPPTS: P(m-C6H4SO3Na)(3)), as catalyst in the presence of cetyl trimethyl ammonium bromide (CTAB) as surfactant to enhance the reaction rate. The reaction was carried out in a batch reactor at pressures from 0.9 to 1.3 MPa and temperatures froth 353 to 373 K. An orthogonal experimental design was adopted to study the effects of operating variables on reaction rate, selectivity and normal/isomeric aldehyde ratio. The optimal reaction conditions were derived by margin and variance analyses. The analysis of mass transfer indicates that in some cases the gas-liquid mass transfer rate is still a controlling factor. An empirical kinetic equation was developed after correcting the effect of mass transfer. Combining mechanisms of homogeneous hydroformylation with interfacial reaction of biphasic hydroformylation, a semi-empirical kinetic equation was also obtained. (C) 2002 Elsevier Science B.V All rights reserved. |
英文摘要 | Hydroformylation of 1-dodecene was studied in a biphasic system using water-soluble rhodium complex, RhCl(CO) (TPPTS)(2) (TPPTS: P(m-C6H4SO3Na)(3)), as catalyst in the presence of cetyl trimethyl ammonium bromide (CTAB) as surfactant to enhance the reaction rate. The reaction was carried out in a batch reactor at pressures from 0.9 to 1.3 MPa and temperatures froth 353 to 373 K. An orthogonal experimental design was adopted to study the effects of operating variables on reaction rate, selectivity and normal/isomeric aldehyde ratio. The optimal reaction conditions were derived by margin and variance analyses. The analysis of mass transfer indicates that in some cases the gas-liquid mass transfer rate is still a controlling factor. An empirical kinetic equation was developed after correcting the effect of mass transfer. Combining mechanisms of homogeneous hydroformylation with interfacial reaction of biphasic hydroformylation, a semi-empirical kinetic equation was also obtained. (C) 2002 Elsevier Science B.V All rights reserved. |
WOS标题词 | Science & Technology ; Physical Sciences ; Technology |
类目[WOS] | Chemistry, Applied ; Chemistry, Physical ; Engineering, Chemical |
研究领域[WOS] | Chemistry ; Engineering |
收录类别 | SCI |
原文出处 | |
语种 | 英语 |
WOS记录号 | WOS:000176407000005 |
公开日期 | 2013-11-12 |
版本 | 出版稿 |
源URL | [http://ir.ipe.ac.cn/handle/122111/5687] ![]() |
专题 | 过程工程研究所_研究所(批量导入) |
作者单位 | Chinese Acad Sci, Inst Chem Met, Beijing 100080, Peoples R China |
推荐引用方式 GB/T 7714 | Zhang, YQ,Mao, ZS,Chen, TY. Macro-kinetics of biphasic hydroformylation of 1-dodecene catalyzed by water-soluble rhodium complex[J]. CATALYSIS TODAY,2002,74(1-2):23-35. |
APA | Zhang, YQ,Mao, ZS,&Chen, TY.(2002).Macro-kinetics of biphasic hydroformylation of 1-dodecene catalyzed by water-soluble rhodium complex.CATALYSIS TODAY,74(1-2),23-35. |
MLA | Zhang, YQ,et al."Macro-kinetics of biphasic hydroformylation of 1-dodecene catalyzed by water-soluble rhodium complex".CATALYSIS TODAY 74.1-2(2002):23-35. |
入库方式: OAI收割
来源:过程工程研究所
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