Zhang Guohua, Liu Min, Han Yaning, Wang Zhongteng, Liu Wei, Zhang Ying, Xu Jing
Jinhua Advanced Research Institute Jinhua Zhejiang 321013 P. R. China
Department of Optical Engineering, College of Optical, Mechanical and Electrical Engineering, Zhejiang A&F University Hangzhou Zhejiang 311300 P. R. China
RSC Adv. 2024 May 1;14(19):13321-13335. doi: 10.1039/d4ra00952e. eCollection 2024 Apr 22.
Aldehydes play a crucial role in the formation of atmospheric particles, attracting significant attention due to their environmental impact. However, the microscopic mechanisms underlying the formation of aldehyde-involved particles remain uncertain. In this study, through quantum chemical calculations and molecular dynamics (MD) simulations, we investigate the microscopic formation mechanisms of binary and ternary systems composed of three representative aldehydes, two sulfur-based acids, water, and two bases. Our research findings reveal that the most stable structures of acid-aldehyde clusters involve the connection of acids and aldehyde compounds through hydrogen bonds without involving proton transfer reactions, indicating relatively poor cluster stability. However, with the introduction of a third component, the stability of 18 clusters significantly increase. Among these, in ten systems, acids act as catalysts, facilitating reactions between aldehyde compounds and water or alkaline substances to generate glycols and amino alcohols. However, according to MD simulations conducted at 300 K, these acids readily dissociate from the resulting products. In the remaining eight systems, the most stable structural feature involves ion pairs formed by proton transfer reactions between acids and aldehyde compounds. These clusters exhibit remarkable thermodynamic stability. Furthermore, the acidity of the acid, the nature of nucleophilic agents, and the type of aldehyde all play significant roles in cluster stability and reactivity, and they have synergistic effects on the nucleation process. This study offers microscopic insights into the processes of new particle formation involving aldehydes, contributing to a deeper understanding of atmospheric chemistry at the molecular level.
醛类在大气颗粒物的形成中起着关键作用,因其对环境的影响而备受关注。然而,涉及醛类的颗粒物形成的微观机制仍不明确。在本研究中,通过量子化学计算和分子动力学(MD)模拟,我们研究了由三种代表性醛类、两种含硫的酸、水和两种碱组成的二元和三元体系的微观形成机制。我们的研究结果表明,酸 - 醛团簇最稳定的结构是酸与醛化合物通过氢键连接,不涉及质子转移反应,这表明团簇稳定性相对较差。然而,随着第三种组分的引入,18种团簇的稳定性显著增加。其中,在十个体系中,酸作为催化剂,促进醛化合物与水或碱性物质之间的反应,生成二醇和氨基醇。然而,根据在300 K下进行的MD模拟,这些酸很容易从生成的产物中解离。在其余八个体系中,最稳定的结构特征是酸与醛化合物之间通过质子转移反应形成离子对。这些团簇表现出显著的热力学稳定性。此外,酸的酸度、亲核试剂的性质以及醛的类型在团簇稳定性和反应性中都起着重要作用,并且它们对成核过程具有协同效应。本研究为涉及醛类的新粒子形成过程提供了微观见解,有助于在分子水平上更深入地理解大气化学。