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甲磺酸、甲胺和草酸混合团簇中的质子转移:对大气颗粒物形成的影响

Proton Transfer in Mixed Clusters of Methanesulfonic Acid, Methylamine, and Oxalic Acid: Implications for Atmospheric Particle Formation.

作者信息

Xu Jing, Finlayson-Pitts Barbara J, Gerber R Benny

机构信息

Department of Chemistry, University of California , Irvine, California 92697-2025, United States.

Institute of Chemistry, Fritz Haber Research Center, Hebrew University of Jerusalem , Jerusalem 91904, Israel.

出版信息

J Phys Chem A. 2017 Mar 30;121(12):2377-2385. doi: 10.1021/acs.jpca.7b01223. Epub 2017 Mar 17.

Abstract

Understanding the properties of atmospheric particles made of several components is a very challenging problem. In this paper, we perform quantum chemical calculations for small multicomponent clusters of atmospheric relevance that incorporate methanesulfonic acid (MSA), methylamine (MA), oxalic acid (OxA), and water (HO). Potential correlations between theoretical predictions of proton transfer in the small clusters and findings of recent experiments on formation of particles of detectable sizes (>2 nm) from the same components are studied. It is proposed that proton transfer from the acid to the amine in the 1:1 clusters correlates with experiments on particle formation in systems, such as MSA-MA and MSA-MA-OxA. In the case of OxA + MA, which has been observed to give few particles, proton transfer does not occur for the 1:1 cluster but does for the 2:2 cluster. Adding HO to OxA-MA promotes the occurrence of proton transfer, and corresponding particles are slightly enhanced. The partial charge on the MA component increases by adding OxA or HO to MSA-MA, which is correlated with enhanced particle formation compared to MSA-MA alone. Ab initio molecular dynamics simulations show that proton transfer at room temperature (T = 298 K) and high temperature (T = 500 K) is little affected compared with the equilibrium structure (T = 0 K). These results suggest that small cluster calculations may be useful in predicting the formation of multicomponent particles in the atmosphere.

摘要

了解由多种成分构成的大气颗粒物的性质是一个极具挑战性的问题。在本文中,我们对与大气相关的多组分小簇合物进行了量子化学计算,这些簇合物包含甲磺酸(MSA)、甲胺(MA)、草酸(OxA)和水(HO)。研究了小簇合物中质子转移的理论预测与近期关于由相同成分形成可检测尺寸(>2 nm)颗粒的实验结果之间的潜在关联。结果表明,1:1簇合物中从酸到胺的质子转移与MSA - MA和MSA - MA - OxA等体系中颗粒形成的实验相关。在OxA + MA的情况下,已观察到形成的颗粒很少,1:1簇合物中不发生质子转移,但2:2簇合物中会发生。向OxA - MA中添加HO会促进质子转移的发生,相应的颗粒略有增加。在MSA - MA中添加OxA或HO会使MA组分上的部分电荷增加,这与单独的MSA - MA相比颗粒形成增强相关。从头算分子动力学模拟表明,与平衡结构(T = 0 K)相比,室温(T = 298 K)和高温(T = 500 K)下的质子转移受影响较小。这些结果表明,小簇合物计算可能有助于预测大气中多组分颗粒的形成。

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