Song Wanrong, Guo Shaoxun, Li Hui
Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, China.
Phys Chem Chem Phys. 2024 Sep 11;26(35):23125-23135. doi: 10.1039/d4cp01752h.
Understanding the accurate acidity of nano-aerosols is important for the research on atmospheric chemistry. Herein, we propose the contributions from both the aerosol size and multiphase buffer effect to the steady-state acidity of nano-aerosols at a constant aerosol water content (AWC) through molecular simulations. As increasing of the aerosol size, the solvation free energy (SFE, Δ) became more negative (decreasing by 3-130 kcal mol for different types of species) and Henry's law constant () apparently increased (from e to e mol m Pa) in the nano-aerosols compared to that in bulk solutions. The lower SFE led to lower solute p and p values; thus, the acidity of HSO and HNO and the alkalinity of NH showed positive relations with the aerosol size. The lower also increased the p of gaseous solutes, leading to a decrease in the acidity of HNO and a shift from alkaline to acidic for the NH/NH buffer pair in the nano-aerosols. The present study revealed the relationship between aerosol acidity and solvent size from a microscopic perspective. Specifically, the acidity of aerosols containing HSO/SO and HNO/NO decreased with an increase in their radii, whereas aerosols containing NH/NH exhibited an opposite trend. This phenomenon can be attributed to the disappearance of the interfacial effect with an increase in the size of the aerosols. The above conclusions are of great significance for studying the pH-dependent multi-phase chemical processes in aerosols.
了解纳米气溶胶的准确酸度对于大气化学研究至关重要。在此,我们通过分子模拟提出了在恒定气溶胶含水量(AWC)下,气溶胶粒径和多相缓冲效应对纳米气溶胶稳态酸度的贡献。与本体溶液相比,随着气溶胶粒径的增加,纳米气溶胶中的溶剂化自由能(SFE,Δ)变得更负(不同类型的物种降低3 - 130 kcal mol),亨利定律常数()明显增加(从e到e mol m Pa)。较低的SFE导致溶质p和p值降低;因此,HSO和HNO的酸度以及NH的碱度与气溶胶粒径呈正相关。较低的也增加了气态溶质的p,导致HNO酸度降低,并且纳米气溶胶中NH/NH缓冲对从碱性转变为酸性。本研究从微观角度揭示了气溶胶酸度与溶剂尺寸之间的关系。具体而言,含有HSO/SO和HNO/NO的气溶胶酸度随着半径的增加而降低,而含有NH/NH的气溶胶则呈现相反的趋势。这种现象可归因于随着气溶胶尺寸的增加界面效应的消失。上述结论对于研究气溶胶中pH依赖的多相化学过程具有重要意义。