Enhanced catalytic performance of Zr modified CuO/ZnO/Al2O3 catalyst for methanol and DME synthesis via CO2 hydrogenation

被引:86
作者
Ren, Shoujie [1 ]
Fan, Xiao [1 ]
Shang, Zeyu [1 ]
Shoemaker, Weston R. [1 ]
Ma, Lu [2 ]
Wu, Tianpin [2 ]
Li, Shiguang [3 ]
Klinghoffer, Naomi B. [3 ]
Yu, Miao [4 ]
Liang, Xinhua [1 ]
机构
[1] Missouri Univ Sci & Technol, Dept Chem & Biochem Engn, Rolla, MO 65409 USA
[2] Argonne Natl Lab, Adv Photon Source, Xray Sci Div, 9700 S Cass Ave, Argonne, IL 60439 USA
[3] Inst Gas Technol, 1700 South Mt Prospect Rd, Des Plaines, IL 60018 USA
[4] Rensselaer Polytech Inst, Dept Chem & Biol Engn, Troy, NY 12180 USA
关键词
CO(2)hydrogenation; Methanol; Dimethyl ether; CuO/ZnO/ZrO2/Al2O3 (CZZA); Stability; DIMETHYL ETHER SYNTHESIS; CU/ZNO/AL2O3; CATALYSTS; STRUCTURAL-CHANGES; SYNGAS; DEACTIVATION; CUO-ZNO-AL2O3; TECHNOLOGIES; CONVERSION; PRECURSOR; EVIDENCES;
D O I
10.1016/j.jcou.2019.11.013
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Zirconium (Zr) modified CuO/ZnO/Al2O3 (CZA) catalysts with different aluminum (Al) and Zr contents were synthesized by the co-precipitation method. The synthesized CuO/ZnO/ZrO2/Al2O3(CZZA) catalysts were comprehensively characterized and studied for methanol synthesis via CO2 hydrogenation. The CZZA catalyst showed the highest methanol yield of 12.4 % at 220 degrees C and 2.76 MPa with an optimized catalyst composition of Cu/Zn/Zr/Al (atomic ratio) at 4:2:1:0.5. The CZZA catalyst showed better activity than that of the CZA catalyst and a superior stability for methanol synthesis. There was no decrease in the BET surface area and very lithe coke formation for the spent CZZA catalyst, after 300 h of methanol synthesis. Bifunctional catalysts, composed of CZZA and HZSM-5, were investigated for dimethyl ether (DME) synthesis directly from CO2 hydrogenation, and a maximum DME yield of 18.3 % was obtained at a reaction temperature of 240 degrees C and a pressure of 2.76 MPa. The stability of the bifunctional CZZA and HZSM-5 catalyst during the DME synthesis also significantly improved, as compared to that of the CZA and HZSM-5. A significant decrease in the BET surface area and an increase in coking on the spent CZZA catalyst were observed after 100 h of DME synthesis, indicating a detrimental effect on CZZA stability when a HZSM-5 catalyst was present. The changes in structural properties (e.g., BET surface area and crystallinity) and coking for HZSM-5 could be responsible for the deactivation of the bifunctional catalyst.
引用
收藏
页码:82 / 95
页数:14
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