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通过臭氧分解评估用于直接空气捕获的吸附剂的长期降解情况。

Assessment of Long-Term Degradation of Adsorbents for Direct Air Capture by Ozonolysis.

作者信息

Jamdade Shubham, Cai Xuqing, Sholl David S

机构信息

School of Chemical & Biomolecular Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332-0100, United States.

Oak Ridge National Laboratory, Oak Ridge, Tennessee 37830, United States.

出版信息

J Phys Chem C Nanomater Interfaces. 2024 Dec 20;129(1):899-909. doi: 10.1021/acs.jpcc.4c07054. eCollection 2025 Jan 9.

Abstract

Porous adsorbents are a promising class of materials for the direct air capture of CO (DAC). Practical implementation of adsorption-based DAC requires adsorbents that can be used for thousands of adsorption-desorption cycles without significant degradation. We examined the potential degradation of adsorbents by a mechanism that appears to have not been considered previously, namely, ozonolysis by trace levels of ozone from ambient air. We focused on amine-appended metal-organic frameworks, specifically amine-functionalized Mg(dobpdc), as a representative DAC adsorbent. Estimates based on the number of amine sites in these adsorbents and the ozone concentration in air suggest that degradation by ozone may be relevant over thousands of adsorption-desorption cycles if reactions with adsorbed ozone are fast. We used density functional theory calculations to estimate reaction rates for amine groups and carbon-carbon double bonds in amine-functionalized Mg(dobpdc).

摘要

多孔吸附剂是用于直接从空气中捕获二氧化碳(DAC)的一类很有前景的材料。基于吸附的DAC的实际应用需要能够用于数千次吸附-解吸循环而不会显著降解的吸附剂。我们通过一种似乎以前未被考虑过的机制来研究吸附剂的潜在降解,即来自环境空气中痕量臭氧的臭氧分解作用。我们重点研究了接枝胺的金属有机框架,特别是胺功能化的Mg(dobpdc),作为DAC吸附剂的代表。根据这些吸附剂中胺位点的数量和空气中的臭氧浓度进行的估计表明,如果与吸附的臭氧的反应很快,那么在数千次吸附-解吸循环中臭氧降解可能是相关的。我们使用密度泛函理论计算来估计胺功能化的Mg(dobpdc)中胺基和碳-碳双键的反应速率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6700/11726669/7a99ba3db3bb/jp4c07054_0001.jpg

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