Xing Lei, Wei Kexin, Li Yuchen, Fang Zhimo, Li Qiangwei, Qi Tieyue, An Shanlong, Zhang Shihan, Wang Lidong
MOE Key Laboratory of Resources and Environmental Systems Optimization, College of Environmental Science and Engineering, North China Electric Power University, Beijing 102206, P. R. China.
Hebei Key Lab of Power Plant Flue Gas Multi-Pollutants Control, Department of Environmental Science and Engineering, North China Electric Power University, Baoding 071003, China.
Environ Sci Technol. 2021 Aug 17;55(16):11216-11224. doi: 10.1021/acs.est.1c02452. Epub 2021 Jul 29.
High energy duty restricts the application of amine-based absorption in CO capture and limits the achievement of carbon neutrality. Although regenerating the amine solvent with solid acid catalysts can increase energy efficiency, inactivation of the catalyst must be addressed. Here, we report a robust metal-organic framework (MOF)-derived hybrid solid acid catalyst (SO/ZIF-67-C@TiO) with improved acidity for promoting amine regeneration. The TiO coating effectively prevented the active components stripping from the surface of the catalyst, thus prolonging its lifespan. The well-protected Co-N sites and protonated groups introduced onto the TiO surface increased the amount and rate of CO desorption by more than 64.5 and 153%, respectively. Consequently, the energy consumption decreased by approximately 36%. The catalyzed N-C bond rupture and proton transfer mechanisms are proposed. This work provides an effective protection strategy for robust acid catalysts, thus advancing the CO capture with less energy duty.
高能量负荷限制了胺基吸收法在二氧化碳捕集中的应用,并限制了碳中和目标的实现。虽然用固体酸催化剂再生胺溶剂可以提高能源效率,但催化剂失活问题必须得到解决。在此,我们报道了一种具有增强酸度的坚固金属有机框架(MOF)衍生的混合固体酸催化剂(SO/ZIF-67-C@TiO),用于促进胺的再生。TiO涂层有效地防止了活性成分从催化剂表面剥离,从而延长了其使用寿命。引入到TiO表面的得到良好保护的Co-N位点和质子化基团分别使二氧化碳解吸量和速率提高了64.5%以上和153%以上。因此,能耗降低了约36%。本文提出了催化N-C键断裂和质子转移机制。这项工作为坚固的酸催化剂提供了一种有效的保护策略,从而以更低的能量负荷推进二氧化碳捕获。