Capture and Methanation of CO2 Using Dual-Function Materials (DFMs)

Anastasios I. Tsiotsias, N. Charisiou, I. Yentekakis, M. Goula
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引用次数: 3

Abstract

The conversion of CO2, captured from flue gases, into synthetic natural gas (SNG) aims to create a closed carbon cycle, where excess H2 produced from renewables is utilized to transform CO2 released from existing conventional power plants into a reliable and high energy density carrier, that is CH4. In the last five years, extensive research effort has been dedicated to the synthesis and optimization of composite materials for the realization of this process. These materials, also known as dual-function materials or DFMs, typically consist of an alkaline metal oxide or carbonate phase, along with a Ru or Ni metallic phase supported on a high surface area carrier. The DFMs incorporate both sorptive and catalytic capabilities, capturing the CO2 in the initial sorption step and then converting it into CH4 upon H2 inflow. The dispersion of the sorptive and catalytically active phases, the CO2 affinity of the alkaline phase, the reducibility of the supported metals, and the selectivity towards CH4 production are some of the parameters influencing their performance. Hereby, we aim to present the most recent works dedicated to the development and optimization of such dual-function materials to be used in the combined capture and methanation of CO2.
将从烟道气中捕获的二氧化碳转化为合成天然气(SNG)的目的是建立一个封闭的碳循环,利用可再生能源产生的多余H2将现有常规发电厂释放的二氧化碳转化为可靠的高能量密度载体,即CH4。在过去的五年中,为了实现这一过程,大量的研究工作一直致力于复合材料的合成和优化。这些材料,也被称为双功能材料或dfm,通常由碱性金属氧化物或碳酸盐相,以及Ru或Ni金属相支撑在高表面积载体上组成。dfm具有吸附和催化能力,在初始吸附步骤中捕获CO2,然后在H2流入时将其转化为CH4。吸附相和催化活性相的分散性、碱相对CO2的亲和性、负载金属的还原性以及对CH4生成的选择性是影响其性能的一些参数。在此,我们旨在展示致力于开发和优化这种双功能材料的最新工作,这些材料将用于二氧化碳的联合捕集和甲烷化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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