Issue 4, 2016

Active and regioselective rhodium catalyst supported on reduced graphene oxide for 1-hexene hydroformylation

Abstract

Alkene hydroformylation with syngas (CO + H2) to produce aldehydes is one of the most important chemical reactions. However, designing heterogeneous catalysts to realize comparable performance with mature homogeneous catalysts is challenging. In this report, a reduced graphene oxide (RGO) supported rhodium nanoparticle (Rh/RGO) catalyst was successfully prepared via a one-pot liquid-phase reduction method and first applied in 1-hexene hydroformylation. 1-Hexene hydroformylation reaction under different reaction conditions with this Rh/RGO catalyst was investigated in detail. Low reaction temperature and short reaction time effectively enhanced the n/i (normal to iso) ratio of heptanal in the products. The catalytic performance of the Rh/RGO catalyst was also compared with those of Rh supported on other carbon materials, including activated carbon and carbon nanotubes (Rh/AC and Rh/CNTs). The results showed that the Rh/RGO catalyst exhibited the highest 1-hexene conversion and the largest n/i ratio of 4.0 among the tested catalysts. The special 2D nanosheet structure of the Rh/RGO catalyst, rather than the 3D porous and 1D nanotube structures of Rh/AC and Rh/CNTs, respectively, principally contributed to its excellent catalytic performance. These findings disclosed that reduced graphene oxide could be a promising catalyst support for designing heterogeneous hydroformylation catalysts.

Graphical abstract: Active and regioselective rhodium catalyst supported on reduced graphene oxide for 1-hexene hydroformylation

Supplementary files

Article information

Article type
Paper
Submitted
18 Aug 2015
Accepted
15 Sep 2015
First published
16 Sep 2015

Catal. Sci. Technol., 2016,6, 1162-1172

Active and regioselective rhodium catalyst supported on reduced graphene oxide for 1-hexene hydroformylation

M. Tan, G. Yang, T. Wang, T. Vitidsant, J. Li, Q. Wei, P. Ai, M. Wu, J. Zheng and N. Tsubaki, Catal. Sci. Technol., 2016, 6, 1162 DOI: 10.1039/C5CY01355K

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