催化作用
吸附
金属间化合物
化学工程
离解(化学)
材料科学
碳纤维
甲烷化
水煤气变换反应
纳米技术
反应机理
反应条件
化学
结构稳定性
无机化学
一氧化碳
一氧化碳中毒
机制(生物学)
化学稳定性
作者
Pengcheng Li,Xinran Cui,Yanlan Ke,Chengxiong Dang,Weiquan Cai
标识
DOI:10.1021/acssuschemeng.6c01485
摘要
Lowering the temperature of the integrated CO2 capture and reverse water–gas shift (ICCU-RWGS, typically above 650 °C) reaction presents great potential for addressing the current challenges of low CO2 conversion, a lack of carbon balance, and severe sintering. Herein, we successfully achieved the ICCU-RWGS reaction at 550 °C using CeO2-modified NiIn-CaO catalysts. Systematic characterizations reveal that the incorporation of CeO2 can modify the electronic structure of NiIn intermetallic compounds (IMCs), which weakens H2 adsorption and dissociation relative to that of CO, thereby preventing further hydrogenation of CO to CH4. Additionally, CeO2 not only exhibits a strong interaction with NiIn IMCs to stabilize particles but also serves as a physical barrier to inhibit structural degradation, thereby guaranteeing the high stability of the catalyst. Consequently, CO2 conversion, CO selectivity, and carbon balance during the entire 50-cycle test remained stable at 94.6, 100, and 98.0%, respectively, and the CO2 adsorption capacity decreased by only 21.5%.
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