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甲磺酸促进单乙醇胺新粒子形成的计算研究。

Methanesulfonic Acid-driven New Particle Formation Enhanced by Monoethanolamine: A Computational Study.

机构信息

Key Laboratory of Industrial Ecology and Environmental Engineering (Ministry of Education), School of Environmental Science and Technology , Dalian University of Technology , Dalian 116024 , China.

Department of Chemistry and iClimate , Aarhus University , Langelandsgade 140 , DK-8000 Aarhus C , Denmark.

出版信息

Environ Sci Technol. 2019 Dec 17;53(24):14387-14397. doi: 10.1021/acs.est.9b05306. Epub 2019 Nov 22.

Abstract

Amines are recognized as significant enhancing species on methanesulfonic acid (MSA)-driven new particle formation (NPF). Monoethanolamine (MEA) has been detected in the atmosphere, and its concentration could be significantly increased once MEA-based postcombustion CO capture technology is widely implemented. Here, we evaluated the enhancing potential of MEA on MSA-driven NPF by examining the formation of MEA-MSA clusters using a combination of quantum chemical calculations and kinetics modeling. The results indicate that the -OH group of MEA can form at least one hydrogen bond with MSA or MEA in all MEA-containing clusters. The enhancing potential of MEA is higher than that of the strongest enhancing agent known so far, methylamine (MA), for MSA-driven NPF. Such high enhancing potential can be ascribed to not only the higher gas-phase basicity but also the role of the additional -OH group of MEA in increasing the binding free energy by forming additional hydrogen bonds. This clarifies the importance of hydrogen-bonding capacity from the nonamino group of amines in enhancing MSA-driven NPF. The main growth pathway for MEA-MSA clusters proceeds via the initial formation of the (MEA)(MSA) cluster, followed by alternately adding one MSA and one MEA molecule, differing from the case of MA-MSA clusters.

摘要

胺被认为是甲磺酸(MSA)驱动的新粒子形成(NPF)中的重要增强物种。单乙醇胺(MEA)已在大气中检测到,一旦广泛实施基于 MEA 的燃烧后 CO 捕集技术,其浓度可能会显著增加。在这里,我们通过结合量子化学计算和动力学模型来评估 MEA 对 MSA 驱动的 NPF 的增强潜力,考察了 MEA-MSA 团簇的形成。结果表明,MEA 的-OH 基团在所有含 MEA 的团簇中至少可以与 MSA 或 MEA 形成一个氢键。MEA 对 MSA 驱动的 NPF 的增强潜力高于迄今为止已知的最强增强剂甲胺(MA)。这种高增强潜力不仅归因于较高的气相碱性,还归因于 MEA 中额外的-OH 基团通过形成额外氢键来增加结合自由能的作用。这阐明了在增强 MSA 驱动的 NPF 中,胺的非氨基的氢键能力的重要性。MEA-MSA 团簇的主要生长途径是通过最初形成(MEA)(MSA)团簇,然后交替添加一个 MSA 和一个 MEA 分子来进行,这与 MA-MSA 团簇的情况不同。

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