质子
解吸
硫黄
电子转移
电子
化学
芯(光纤)
分析化学(期刊)
材料科学
物理化学
吸附
环境化学
物理
核物理学
有机化学
复合材料
作者
Lei Xing,Zhen Chen,Guoxiong Zhan,Zhoulan Huang,Mingyue Li,Yuchen Li,Lidong Wang,Junhua Li
标识
DOI:10.1021/acs.est.3c09875
摘要
Transforming hazardous species into active sites by ingenious material design was a promising and positive strategy to improve catalytic reactions in industrial applications. To synergistically address the issue of sluggish CO 2 desorption kinetics and SO 2 -poisoning solvent of amine scrubbing, we propose a novel method for preparing a high-performance core–shell C@Mn 3 O 4 catalyst for heterogeneous sulfur migration and in situ reconstruction to active –SO 3 H groups, and thus inducing an enhanced proton-coupled electron transfer (PCET) effect for CO 2 desorption. As anticipated, the rate of CO 2 desorption increases significantly, by 255%, when SO 2 is introduced. On a bench scale, dynamic CO 2 capture experiments reveal that the catalytic regeneration heat duty of SO 2 -poisoned solvent experiences a 32% reduction compared to the blank case, while the durability of the catalyst is confirmed. Thus, the enhanced PCET of C@Mn 3 O 4, facilitated by sulfur migration and simultaneous transformation, effectively improves the SO 2 resistance and regeneration efficiency of amine solvents, providing a novel route for pursuing cost-effective CO 2 capture with an amine solvent.
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