Ma Shuaishuai, Fan Younuo, Tang Yingying, He Chengxiang, Li Qiong, Zhao Zhiqing, Xu Tianyou, Zhang Yunhong
College of Chemical and Material Engineering, Quzhou University, Quzhou 324000, China.
Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention, Department of Environmental Science & Engineering, Fudan University, Shanghai 200433, China.
J Phys Chem A. 2024 Aug 1;128(30):6286-6295. doi: 10.1021/acs.jpca.4c03107. Epub 2024 Jul 23.
The deliquescence phase transition of atmospheric aerosols is crucial for radiative forcing and atmospheric chemistry. However, the deliquescence kinetics of micrometer-sized aerosols, especially the formation and evolution of surface solution films, remain poorly understood. In this study, IR spectral characteristics were employed for the first time to quantify the solute concentration evolution in surface solution films. At a constant relative humidity (RH) of ∼65%, solution films on NaCl crystals exhibited a very low solute concentration (3.06 ± 0.18 mol/L), comparable to aqueous NaCl droplets above 90% RH. These films reached saturation at ∼74% RH, i.e., the deliquescence RH of NaCl, maintaining a nearly constant saturation level during deliquescence. In contrast, amorphous NaNO solids showed supersaturated solution films before deliquescence. Following deliquescence, the saturation level of solution phases increased due to faster solid dissolution rates than liquid water condensation. These findings address knowledge gaps in the complex nonequilibrium dissolution processes of crystalline or amorphous atmospheric aerosols.
大气气溶胶的潮解相变对于辐射强迫和大气化学至关重要。然而,微米级气溶胶的潮解动力学,尤其是表面溶液膜的形成和演化,仍知之甚少。在本研究中,首次采用红外光谱特征来量化表面溶液膜中溶质浓度的演变。在约65%的恒定相对湿度(RH)下,NaCl晶体上的溶液膜显示出非常低的溶质浓度(3.06±0.18 mol/L),与相对湿度高于90%的NaCl水滴相当。这些膜在约74%RH时达到饱和,即NaCl的潮解相对湿度,在潮解过程中保持几乎恒定的饱和水平。相比之下,无定形NaNO固体在潮解前显示出过饱和溶液膜。潮解后,由于固体溶解速度比液态水凝结速度快,溶液相的饱和水平增加。这些发现填补了结晶或无定形大气气溶胶复杂非平衡溶解过程中的知识空白。