Direct coating copper-zinc-aluminum oxalate with H-ZSM-5 to fabricate a highly efficient capsule-structured bifunctional catalyst for dimethyl ether production from syngas

被引:13
作者
Sun, Yingqi [1 ]
Han, Xinghua [2 ]
Zhao, Zhongkui [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, Dept Catalysis Chem & Engn, State Key Lab Fine Chem, 2 Linggong Rd, Dalian 116024, Peoples R China
[2] North Univ China, Sch Chem Engn & Technol, Taiyuan 030051, Shanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
DIRECT DME SYNTHESIS; HYBRID CATALYSTS; METHANOL DEHYDRATION; CO2; HYDROGENATION; CARBON-DIOXIDE; ACID SITES; ZEOLITE; DEACTIVATION; CONVERSION; OXIDE;
D O I
10.1039/c9cy00980a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Dimethyl ether (DME) has been considered as an industrially important intermediate and clean alternative fuel. The development of a highly efficient syngas-to-DME bifunctional catalyst is of great importance but remains a challenge. In this work, we reported a facile and robust strategy for preparing a highly efficient CZA-oa@H-ZSM-5 capsule-structured bifunctional catalyst by coating an H-ZSM-5 shell on millimeter-sized copper-zinc-aluminum oxalate (CZA-oa) but not on copper-zinc-aluminum oxide (CZA-oxi) via the hydrothermal crystallization process with the subsequent calcination at 500 degrees C for 5 h in air. From the characterization and reaction results, we inferred that the direct use of CZA-oa as a replacement of CZA efficiently inhibited Cu leaching in the coating process, besides turning down the necessity of using a rotary oven for the good coating of the H-ZSM-5 shell on the core owing to high hydrophilic property. The developed CZA-oa@H-ZSM-5 capsule bifunctional catalyst showed 5.0 times higher turnover frequency (TOF, 1.5 min(-1)) with 93.7% of DME selectivity as compared to CZA-oxi@H-ZSM-5 R (0.3 min(-1) of TOF and 92.5% of DME selectivity) prepared by a similar procedure except for the use of mixed oxide as a core to replace CZA-oa. The improvement in the intrinsic activity of the developed CZA-oa@H-ZSM-5 capsule bifunctional catalyst originated from appropriate Cu-Zn interactions. Interestingly, owing to the excellent hydrophilic property of CZA-oa, the use of the rotary oven in the coating process of the H-ZSM-5 shell can be avoided if oxalate is used to replace oxide as a core. Compared to CZA-oxi@H-ZSM-5 R (0.031 mmol m(Cu)(-2) h(-1)), CZA-oa@H-ZSM-5 showed a much higher DME formation rate (R-DME = 0.122 mmol m(Cu)(-2) h(-1)), which allowed it to be a promising catalyst for DME production from syngas. Moreover, this work also opens a new window for designing outstanding bifunctional catalysts for other applications.
引用
收藏
页码:3763 / 3770
页数:8
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