Back to Search Start Over

Synthesis of Propylene Carbonate from Carbon Dioxide and Propylene Oxide Using Zn- Mg-Al Composite Oxide as High-efficiency Catalyst.

Authors :
Wei-Li Dai
Shuang-Feng Yin
Rui Guo
Sheng-Lian Luo
Xin Du
Chak-Tong Au
Source :
Catalysis Letters; May2010, Vol. 136 Issue 1/2, p35-44, 10p, 3 Diagrams, 4 Charts, 8 Graphs
Publication Year :
2010

Abstract

A series of Zn-Al composite oxides that were modified with alkaline earth metals, Zn- M-Al-O ( M = Mg, Ca, Sr, and Ba) were fabricated via calcination of the corresponding hydrotalcite precursors, and evaluated as catalysts for the synthesis of propylene carbonate (PC) from CO<subscript>2</subscript> and propylene oxide. Among the Zn- M-Al-O catalysts, Zn- Mg-Al-O (Zn/Mg = 4.0, pH = 10, without hydrothermal treatment) is the best in performance, showing PC selectivity of 99.2% and yield of 88.8% (140 °C, 12 h). Furthermore, the Zn- Mg-Al-O catalyst can be readily reused and recycled without any loss of activity in a test of five cycles. Through detailed studies of the basic nature of the Zn- M-Al-O catalysts, it was found that a moderate basicity (6.1 ≤ H<subscript>0</subscript> < 8.9) is beneficial to the cycloaddition reaction. The NH<subscript>3</subscript>- and CO<subscript>2</subscript>-TPD results also indicate that the Zn- Mg-Al-O catalyst has acid–base bifunctional properties, and a reaction mechanism is proposed. Zn-Mg-Al composite oxides were prepared via calcination of the corresponding hydrotalcite precursors, and used as catalysts for the synthesis of propylene carbonate from CO<subscript>2</subscript> and propylene oxide. We achieved high catalytic efficiency under mild conditions, easy separation of catalyst from the product, and good recyclability of the catalyst. A plausible reaction mechanism has been proposed for the catalytic action.[Figure not available: see fulltext.] [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1011372X
Volume :
136
Issue :
1/2
Database :
Complementary Index
Journal :
Catalysis Letters
Publication Type :
Academic Journal
Accession number :
49731666
Full Text :
https://doi.org/10.1007/s10562-009-0198-2