Sinopoli Alessandro, Abotaleb Ahmed, Pietrucci Fabio, Gladich Ivan
Qatar Environment and Energy Research Institute, Hamad Bin Khalifa University, P.O. Box 34410, Doha, Qatar.
Sorbonne Université, Muséum National d'Histoire Naturelle, UMR CNRS 7590, IMPMC, 75005 Paris, France.
J Phys Chem B. 2021 May 13;125(18):4890-4897. doi: 10.1021/acs.jpcb.1c01661. Epub 2021 Apr 22.
The need to chemically convert CO at the interface of aqueous amine solutions has become particularly relevant for the development and the broad distribution of cost-effective and near-future devices for direct air capture working at low (e.g., ambient) partial pressure. Here, we have determined the stability of a CO-monoethanolamine zwitterion and its chemical conversion into carbamate at the vapor/liquid water interface by first-principles molecular dynamics simulations coupled with a recently introduced enhanced sampling technique. Contrary to the bulk water case, our results show that both the zwitterion and carbamate ions are poorly stable at the vapor/amine aqueous interface, further stating the differences between the homogeneous and heterogeneous CO chemical conversion. The design of novel and cost-effective capture systems, such as those offered by amine-based scrubbing solutions, working at low (e.g., ambient) CO partial pressure should explore the use of novel solvents, different from aqueous mixtures, to overcome the limits of the current absorbents.
对于开发和广泛应用在低(如环境)分压下工作的具有成本效益且在不久的将来可直接空气捕获的装置而言,在胺水溶液界面上对一氧化碳进行化学转化变得尤为重要。在此,我们通过第一性原理分子动力学模拟结合最近引入的增强采样技术,确定了一氧化碳 - 单乙醇胺两性离子在气/液水界面处的稳定性及其向氨基甲酸盐的化学转化。与本体水情况相反,我们的结果表明,两性离子和氨基甲酸盐离子在气/胺水溶液界面处稳定性较差,进一步说明了均相和非均相一氧化碳化学转化之间的差异。设计新型且具有成本效益的捕获系统,例如基于胺的洗涤溶液在低(如环境)一氧化碳分压下工作的系统,应探索使用不同于水性混合物的新型溶剂,以克服当前吸收剂的局限性。