双金属片
甲烷化
催化作用
烧结
焦炭
水滑石
材料科学
化学工程
金属
多相催化
无机化学
化学
冶金
有机化学
工程类
作者
Xiaorui Wang,Rongrong Jin,Wangwei Yan,Haomiao Li,Zhou‐jun Wang
标识
DOI:10.1016/j.cattod.2022.02.019
摘要
The unsatisfactory low-temperature activity of Ni based catalysts in CO2 methanation calls for further optimization of catalyst design. In the present work, an efficient Ni7Fe1/Al2O3 bimetallic catalyst was derived from hydrotalcite precursors that were grown in-situ on the commercial γ-Al2O3. The resultant Ni7Fe1/Al2O3 bimetallic catalyst exhibited exceptional low-temperature activity, whose CO2 conversion reached 75.3% at 270 ºC under atmospheric pressure. Moreover, the Ni7Fe1/Al2O3 catalyst remained stable at 350 ºC for 50 h. Structural characterizations revealed that the exceptional activity over the bimetallic catalyst was closely related with the formation of NiFe alloy, which modified the electronic property, enhanced the metal reducibility and enriched the surface basic sites of Ni catalysts. The good stability on the bimetallic catalyst was mainly ascribed to the excellent coke- and sintering- resistance. This work develops an efficient methanation catalyst and clarifies the effect of bimetallic synergism in CO2 methanation.
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