接触器
电解
碳酸盐
工艺工程
环境科学
材料科学
化学
工程类
电解质
热力学
功率(物理)
物理
电极
冶金
物理化学
作者
Hussain M. Almajed,Recep Kaş,Paige Brimley,Allison M. Crow,Ana Somoza-Tornos,Bri‐Mathias Hodge,Thomas Burdyny,Wilson A. Smith
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-05-01
卷期号:9 (5): 2472-2483
被引量:37
标识
DOI:10.1021/acsenergylett.4c00807
摘要
CO2 from carbonate-based capture solutions requires a substantial energy input. Replacing this step with (bi)carbonate electrolysis has been commonly proposed as an efficient alternative that coproduces CO/syngas. Here, we assess the feasibility of directly integrating air contactors with (bi)carbonate electrolyzers by leveraging process, multiphysics, microkinetic, and technoeconomic models. We show that the copresence of CO32– with HCO3– in the contactor effluent greatly diminishes the electrolyzer performance and eventually results in a reduced CO2 capture fraction to ≤1%. Additionally, we estimate suitable effluents for (bi)carbonate electrolysis to require 5–14 times larger contactors than conventionally needed contactors, leading to unfavorable process economics. Notably, we show that the regeneration of the capture solvent inside (bi)carbonate electrolyzers is insufficient for CO2 recapture. Thus, we suggest process modifications that would allow this route to be operationally feasible. Overall, this work sheds light on the practical operation of integrated direct air capture with (bi)carbonate electrolysis.
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