Heteropoly Blue as a Reaction-Controlled Phase-Transfer Catalyst for the Epoxidation of Olefins

2005 ◽  
Vol 78 (8) ◽  
pp. 1575-1579 ◽  
Author(s):  
Li Mingqiang ◽  
Jian Xigao
Keyword(s):  
Phase Transfer ◽  
Phase Transfer Catalyst ◽  
Epoxidation Of Olefins

scholarly journals Amphiphilic peroxo polyoxometalate as reaction control phase transfer catalyst for efficient epoxidation of olefins

2021 ◽  
Author(s):  
Jinghui Wu ◽  
Hongwei Zheng ◽  
Chi Wang ◽  
Xianze Wang ◽  
Xiaohong Wang ◽  
...  
Keyword(s):  
Phase Transfer ◽  
Phase Transfer Catalyst ◽  
Control Phase ◽  
Epoxidation Of Olefins

β-cyclodextrin grafted on lignin as inverse phase transfer catalyst for the oxidation of benzyl alcohol in H2O

Tetrahedron ◽  
2016 ◽  
Vol 72 (14) ◽  
pp. 1773-1781 ◽  
Author(s):  
Zujin Yang ◽  
Xia Zhang ◽  
Xingdong Yao ◽  
Yanxiong Fang ◽  
Hongyan Chen ◽  
...  
Keyword(s):  
Benzyl Alcohol ◽  
Phase Transfer ◽  
Phase Transfer Catalyst ◽  
Oxidation Of Benzyl Alcohol ◽  
Inverse Phase Transfer Catalyst

Microwave Energy Pretreated In Situ Transesterification of Jatropha Curcas L in the Presence of Phase Transfer Catalyst

2014 ◽  
Vol 625 ◽  
pp. 267-270 ◽  
Author(s):  
Sintayehu Mekuria Hailegiorgis ◽  
Mahadzir Shuhaimi ◽  
Duvvuri Subbarao
Keyword(s):  
Statistical Model ◽  
Jatropha Curcas ◽  
Phase Transfer ◽  
Phase Transfer Catalyst ◽  
In Situ Transesterification ◽  
Heat Pretreatment ◽  
Seed Particles ◽  
Optimum Reaction ◽  
Microwave Heat

In the present work, microwave heat pretreatment of jatropha curcas seed particles and use of phase transfer catalyst (PTC) to enhance in-situ transesterification were utilized together. It was observed that use of alkaline BTMAOH as a PTC and microwave heat pretreatment of jatropha curcas seed particles had substantially increased the reaction rate of in-situ transesterification as compared to the reaction conducted with microwave untreated seeds in the absence of BTMAOH as a PTC. Statistical model equation was developed to investigate the interaction effect of reaction variables and establish optimum reaction condition. At optimum condition, experimentally obtained FAME yield (93.7±1.53% w/w) was in close agreement with statistical model predicted FAME yield (96.75%) at 38°C and 37 minutes of reaction time.

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