Promotion of surface oxygen vacancies on the light olefins synthesis from catalytic CO2 hydrogenation over Fe-K/ZrO2 catalysts

被引:68
作者
Gu, Hao [1 ]
Ding, Jie [1 ]
Zhong, Qin [1 ]
Zeng, Yiqing [1 ]
Song, Fujiao [2 ]
机构
[1] Nanjing Univ Sci & Technol, Sch Chem Engn, Nanjing 210094, Jiangsu, Peoples R China
[2] Yancheng Inst Technol, Sch Environm Sci & Engn, Yancheng 224000, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
m-ZrO2; t-ZrO2; CO2; hydrogenation; Light olefins; Oxygen vacancies; METHANOL SYNTHESIS; PHOTOLUMINESCENCE PROPERTIES; ZIRCONIA MORPHOLOGY; ZRO2; NANOSTRUCTURES; NANOPARTICLES; REDUCTION; EVOLUTION; PHASE; DYE; H-2;
D O I
10.1016/j.ijhydene.2019.03.046
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
The performance of K and Fe loaded ZrO2 species (Fe-K/ZrO2) for CO2 hydrogenation was relevant to the concentration of oxygen vacancies due to the differences of ZrO2 crystal phases. The K and Fe were deposited on the surface of monoclinic zirconia (m-ZrO2) and tetragonal zirconia (t-ZrO2) with the Fe loading of 0-20 wt% and the K loading of 1 wt% by impregnation methods. The ZrO2 served as both a support and a co-catalyst for CO2 hydrogenation, exhibiting 40.54% CO2 conversion and 14.98% light olefins selectivity over the 10Fe-1K/m-ZrO2 with 10 wt% Fe and 1 wt% K, at 2.0 MPa and 340 degrees C. Such CO2 conversion were almost 200% higher than that of 10Fe-1K/t-ZrO2. The better activity of 10Fe-1K/m-ZrO2 is mainly attributed to the higher concentration of oxygen vacancies on the surface of m-ZrO2 after the reduction in H-2/N-2. However, covering the surface of m-ZrO2, excess surface Fe species lowered the concentration of surface oxygen vacancies for reduced 10Fe-1K/t-ZrO2, which inhibited the catalytic performance of ZrO2 for CO2 conversion. These investigations may propel the utilization of Zr-based catalysts on CO2 hydrogenation to various value-added chemicals. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:11808 / 11816
页数:9
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