环境科学
工艺工程
材料科学
废物管理
化学
工程类
作者
Yongwook Kim,Marzieh Namdari,Andrew Jewlal,Yifu Chen,Douglas J. D. Pimlott,Monika Stolar,Curtis P. Berlinguette
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-12-23
卷期号:: 403-409
标识
DOI:10.1021/acsenergylett.4c02852
摘要
The capture of CO2 using alkaline solutions requires significant thermal energy to release CO2 from a (bi)carbonate-enriched solution. This release of CO2 can instead be performed electrochemically with a "bicarbonate electrolyzer". The bicarbonate electrolyzer forms acid equivalents to convert a (bi)carbonate-enriched eluent from a CO2 capture unit into CO2 and, in turn, an upgraded carbon product such as CO and ethylene. There exists a tension for this closed-loop cycle to be put into practice: a smaller CO2 capture unit is required when using a more caustic CO2 capture solution, yet the electrolyzer works more effectively at a lower pH. Here, we elaborate on three different methods to align different pH regimes to couple air capture to CO2 electrolysis. We also use a mass-balance model to assess the commercial viability of a reactive carbon capture system that integrates the CO2 capture unit with a bicarbonate electrolyzer to show a levelized CO breakeven price below $1 kgCO–1. These economics, coupled with the other practical advantages of providing an electrolyzer with a liquid feedstock, present a compelling case for reactive carbon capture.
科研通智能强力驱动
Strongly Powered by AbleSci AI