Cu/MgO Reverse Water Gas Shift Catalyst with Unique CO2 Adsorption Behaviors

被引:3
作者
Tsai, Ding-Huei [1 ]
Wu, Tung-Ta [2 ,3 ]
Lin, Hung-Chin [1 ]
Chueh, Lu-Yu [1 ]
Lin, Kun-Han [1 ]
Yu, Wen-Yueh [2 ,3 ]
Pan, Yung-Tin [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Chem Engn, 101 Sec 2,Kuang Fu Rd, Hsinchu City 300044, Taiwan
[2] Natl Taiwan Univ, Dept Chem Engn, 1 Sec 4,Roosevelt Rd, Taipei City 106319, Taiwan
[3] Natl Taiwan Univ, Adv Res Ctr Green Mat Sci & Technol, 1 Sect 4,Roosevelt Rd, Taipei City 106319, Taiwan
关键词
RWGS; MgO; Copper; CO2-IR-TPD; OXIDATIVE CARBONYLATION; DIMETHYL CARBONATE; BASIC SITES; SURFACE; HYDROGENATION; DESORPTION; CONVERSION; MECHANISM; METHANOL; CLUSTER;
D O I
10.1002/asia.202300955
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Activation of inert CO2 molecules for the reverse water gas shift (RWGS) reaction is tackled by incorporating magnesium oxide as a support material for copper, forming a Cu/MgO supported catalyst. The RWGS performance is greatly improved when compared with pure Cu or carbon supported Cu (Cu/C). Operating under a weight hourly space velocity (WHSV) of 300,000 mL & sdot; g(-1) & sdot; h(-1), the Cu/MgO catalyst demonstrates high activity, maintaining over 70 % equilibrium conversion and nearly 100 % CO selectivity in a temperature range of 300-600 degrees C. In contrast, both Cu/C and commercial Cu, even at ten-times lower WHSV, can only achieve up to 40 % of the equilibrium conversion and quickly deactivated due to sintering. Based on the studies of in-situ temperature resolved infrared spectroscopy and temperature programmed desorption, the improved RWGS performance is attributed to the unique adsorption behavior of CO2 on Cu/MgO. Density functional theory studies provides a plausible explanation from a surface reaction perspective and reveals the spill-over property of CO2 from MgO to Cu being critical.
引用
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页数:8
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