Multi-walled carbon nanotube-based composite materials as catalyst support for water–gas shift and hydroformylation reactions

氢甲酰化 催化作用 复合数 碳纳米管 水煤气变换反应 化学工程 材料科学 纳米技术 复合材料 化学 有机化学 工程类
作者
Patrick Wolf,Morten Logemann,Markus Schörner,Laura Keller,Marco Haumann,Matthias Weßling
出处
期刊:RSC Advances [Royal Society of Chemistry]
卷期号:9 (47): 27732-27742 被引量:20
标识
DOI:10.1039/c9ra04830h
摘要

In times of depleting fossil fuel reserves, optimizing industrial catalytic reactions has become increasingly important. One possibility for optimization is the use of homogenous catalysts, which are advantageous over heterogeneous catalysts because of mild reaction conditions as well as higher selectivity and activity. A new emerging technology, supported ionic liquid phase (SILP), was developed to permanently immobilize homogeneous catalyst complexes for continuous processes. However, these SILP catalysts are unable to form freestanding supports by themselves. This study presents a new method to introduce the SILP system into a support made from multi-walled carbon nanotubes (MWCNT). In a first step, SILP catalysts were prepared for hydroformylation as well as low-temperature water-gas shift (WGS) reactions. These catalysts were integrated into freestanding microtubes formed from MWCNTs, with silica (for hydroformylation) or alumina particles (for WGS) incorporated. In hydroformylation, the activity increased significantly by around 400% when the pure MWCNT material was used as SILP support. An opposite trend was observed for WGS, where pure alumina particles exhibited the highest activity. A significant advantage of the MWCNT composite materials is the possibility to coat them with separation layers, which allows their application in membrane reactors for more efficient processes.
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