Preparation of Cu-Al2O3-TiO2-Ti3C2/HZSM-5 Catalysts for Catalytic CO2 Hydrogenation to Dimethyl Ether

被引:0
|
作者
Yang, Yanping [1 ]
Su, Tongming [1 ]
Xie, Xinling [1 ]
Luo, Xuan [1 ]
Ji, Hongbing [1 ,2 ]
Sin, Jin-Chung [3 ]
Lam, Sze-Mun [3 ]
Qin, Zuzeng [1 ]
机构
[1] Guangxi Univ, Sch Chem & Chem Engn, Nanning 530004, Peoples R China
[2] Zhejiang Univ Technol, Inst Green Petr Proc & Light Hydrocarbon Convers, Coll Chem Engn, Hangzhou 310014, Peoples R China
[3] Univ Tunku Abdul Rahman, Fac Engn & Green Technol, Jalan Univ, Kampar 31900, Perak, Malaysia
基金
中国国家自然科学基金;
关键词
Cu-based catalysts; Ti3C2; Catalytic CO2 hydrogenation; Dimethyl ether; TEMPERATURE-PROGRAMMED DESORPTION; HYDROTALCITE-LIKE PRECURSORS; CU-BASED CATALYSTS; CARBON-DIOXIDE; METHANOL-SYNTHESIS; INTRINSIC KINETICS; FORMIC-ACID; PERFORMANCE; ADSORPTION; SELECTIVITY;
D O I
10.1007/s10562-024-04828-2
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
To develop efficient catalysts for CO2 hydrogenation to dimethyl ether, Cu-Al2O3-TiO2-Ti3C2/HZSM-5 bifunctional catalysts were prepared by the surfactant PVP-assisted coprecipitation. The influence of Ti3C2 on Cu-Al2O3-based catalysts was investigated. The characterization results revealed that slight oxidation of the Ti3C2 surface generated highly dispersed TiO2 nanoparticles that the doping of TiO2-Ti3C2 in the Cu-Al2O3 catalyst increased the specific surface area of the catalyst and promoted the formation and growth of Cu nanoparticles, and that strong interactions occurred between TiO2-Ti3C2 and the Cu components. The number of oxygen vacancies at the interface between TiO2-Ti3C2 and Cu increased by 17%, and the electronic kinetic energy of Cu-0 decreased by 0.1 eV, with the electron-rich oxygen vacancies transferring electrons to Cu2+ ions and maintaining more Cu species in lower oxidation states. Reactions were carried out at 260 degrees C and 3.0 MPa with a gaseous hourly space velocity (GHSV) of 1500 cm(3.)g(-1).h(-1) using Cu-Al2O3-TiO2-Ti3C2/HZSM-5 with 5.0 wt% Ti3C2 as the hydrogenation catalyst, which provided a CO2 conversion of 26.8% with 57.8% selectivity for DME.
引用
收藏
页码:6454 / 6468
页数:15
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