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Phosgene-Free Synthesis of Phenyl Isocyanate by Catalytic Decomposition of Methyl N-Phenyl Carbamate over Bi2O3 Catalyst.

Authors :
Yunsheng Dai
Yue Wang
Jie Yao
Qingyin Wang
Liangming Liu
Wei Chu
Gongying Wang
Source :
Catalysis Letters; Aug2008, Vol. 123 Issue 3/4, p307-316, 10p, 1 Black and White Photograph, 4 Diagrams, 2 Charts, 9 Graphs
Publication Year :
2008

Abstract

A phosgene-free approach for the synthesis of phenyl isocyanate (PI) was developed, using the heterogeneous catalytic decomposition of methyl N-phenyl carbamate (MPC). Twenty oxide-catalysts were investigated and compared; the Bi<subscript>2</subscript>O<subscript>3</subscript> catalyst gave the better catalytic performance. From bismuth (III) nitrate pentahydrate, Bi<subscript>2</subscript>O<subscript>3</subscript> was prepared by different methods, which included the direct decomposition, mechano-chemical method, direct precipitation and indirect precipitation. The catalysts were characterized by N<subscript>2 </subscript>adsorption/desorption, XRD, FTIR and TEM analyses. After optimization, the Bi<subscript>2</subscript>O<subscript>3</subscript> catalyst prepared by direct calcination of bismuth (III) nitrate pentahydrate at 723 K in air for 4 h gives the best activity. When the reaction was carried out at the boiling temperature of o-dichlorobenzene (ODCB) at normal pressure, the optimal reaction conditions over Bi<subscript>2</subscript>O<subscript>3</subscript> catalyst are as follows: the mass ratio of catalyst/MPC is 0.05, mass ratio of ODCB/MPC is 15:1, reaction time of 60 min. The optimized conversion of MPC and the yield of PI are 86.2% and 78.5%, respectively. There was a good durability for the Bi<subscript>2</subscript>O<subscript>3</subscript> catalyst, and the species of Bi (III) ions of catalyst were partially oxidized to Bi (IV) ions during the reaction, supported by the results of XRD and XPS techniques. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1011372X
Volume :
123
Issue :
3/4
Database :
Complementary Index
Journal :
Catalysis Letters
Publication Type :
Academic Journal
Accession number :
32679736
Full Text :
https://doi.org/10.1007/s10562-008-9424-6