In the present paper, the variational transition-state theory (VTST) method has been used to carry out the dynamical calculations for the D Γ + H 2 ? HD + H Γ reaction and the H Γ + D 2 ? HD + D Γ reaction, respectively. The investigation of the variation of the potential energy curves and the bond
Hydroformylation of propylene in supercritical CO2 + H2O and supercritical propylene + H2O
β Scribed by Zhang Jingchang; Wang Hongbin; Liu Hongtao; Cao Weiliang
- Publisher
- Elsevier Science
- Year
- 2006
- Tongue
- English
- Weight
- 454 KB
- Volume
- 260
- Category
- Article
- ISSN
- 1381-1169
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β¦ Synopsis
Hydroformylation of propylene has been carried out in supercritical CO 2 + H 2 O and in supercritical propylene + H 2 O mixtures using Rh(acac)(CO) 2 and triphenylphosphine trisulfonate trisodium salt (TPPTS), P(m-C 6 H 4 SO 3 Na) 3 , as catalyst. Visual observation of the reaction mixtures indicates that in both systems a single phase is present at supercritical temperatures and pressures so that the reaction occurs under homogeneous conditions. After reaction is complete, a biphasic system is formed when the pressure and temperature are reduced to ambient. This facilitates separation of the products in the organic phase and the rhodium catalyst in the aqueous phase. The rhodium concentration in the organic phase was found to be negligible (βΌ1.0 Γ 10 -6 mg/ml). Furthermore, compared with traditional hydroformylation technology, the supercritical reactions also show better activity and selectivity.
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