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Synthesis of Propylene Carbonate from Carbon Dioxide and Propylene Oxide Using Zn- Mg-Al Composite Oxide as High-efficiency Catalyst.
- 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]
- Subjects :
- PROPYLENE carbonate
ALKALINE earth metals
CARBON dioxide
PROPYLENE oxide
CATALYSTS
Subjects
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