MOE & Guangdong Province Key Laboratory of Laser Life Science & Institute of Laser Life Science, Guangzhou Key Laboratory of Spectral Analysis and Functional Probes, College of Biophotonics, South China Normal University, Guangzhou 510631, P. R. China.
National-Regional Joint Engineering Research Center for Soil Pollution Control and Remediation in South China, Guangdong Key Laboratory of Integrated Agro-environmental Pollution Control and Management, Institute of Eco-environmental and Soil Sciences, Guangdong Academy of Sciences, Guangzhou 510650, P. R. China.
J Am Chem Soc. 2022 Sep 21;144(37):16953-16964. doi: 10.1021/jacs.2c05807. Epub 2022 Sep 7.
Organosulfates (OSs) are well-known and ubiquitous constituents of atmospheric aerosol particles and have been used as secondary organic aerosol markers in many field studies. Hence, it is imperative to understand the formation of OS species in the atmosphere. Recently, hydroxy acids (HAs) and hydroxy acid sulfates have been extensively detected in the atmospheric environment. However, the reaction mechanism of HAs to form OSs is much less understood. In this work, we have mainly investigated the reaction of typical α-HAs, including glycolic acid (GA) and lactic acid (LA), and SO at the liquid aerosol surface using quantum chemistry calculations and Born-Oppenheimer molecular dynamics simulations. The OH group orientation of α-HAs at the air-water interface is found to exert a significant impact on the formation of OSs. The OH group pointing to the gas phase is obviously beneficial to the formation of OSs. Two key factors are discovered important to the reaction of α-HAs adsorbed on the liquid surface with SO: (a) the exposure position of the active site to the gas phase and (b) the reactivity of the exposed site to the attracted SO molecule. Moreover, we found that the air-water interface exerts a significant influence on the physicochemical behaviors of GA and LA, especially on their OH group orientation, and thus leads to their different properties for the SO colliding reaction. The presented reaction mechanism provides a new feasible pathway for the production of OSs at the liquid aerosol surface, which may have important impacts on the formation of organic aerosols.
有机硫酸盐(OSs)是大气气溶胶颗粒中众所周知且普遍存在的成分,并且已被许多实地研究用作次生有机气溶胶的标志物。因此,了解 OS 物质在大气中的形成至关重要。最近,羟酸(HAs)和羟酸硫酸盐已在大气环境中广泛检测到。然而,HAs 形成 OS 的反应机制却鲜为人知。在这项工作中,我们主要使用量子化学计算和 Born-Oppenheimer 分子动力学模拟研究了典型的α-HAs(包括乙醇酸(GA)和乳酸(LA))与 SO 在液滴气溶胶表面的反应。在气-液界面上,α-HAs 的 OH 基团取向对 OSs 的形成有显著影响。OH 基团指向气相有利于 OSs 的形成。发现了两个关键因素对吸附在液面上的α-HAs 与 SO 反应很重要:(a)活性位点向气相的暴露位置,以及(b)暴露位置对被吸引的 SO 分子的反应性。此外,我们发现气-液界面对 GA 和 LA 的物理化学行为有显著影响,特别是对其 OH 基团的取向,从而导致它们在与 SO 碰撞反应时具有不同的性质。所提出的反应机制为液滴气溶胶表面 OSs 的产生提供了新的可行途径,这可能对有机气溶胶的形成有重要影响。