Department of Chemistry, McGill University, 801 Sherbrooke Street West, Montreal, Quebec H3A 0B8, Canada.
Department of Atmospheric and Oceanic Sciences, McGill University, 805 Sherbrooke Street West, Montreal, Quebec, Canada H3A 0B9.
Environ Sci Technol. 2023 Nov 7;57(44):16974-16988. doi: 10.1021/acs.est.3c02894. Epub 2023 Oct 26.
The partitioning of semivolatile organic compounds (SVOCs) between the condensed and gas phases can have significant implications for the properties of aerosol particles. In addition to affecting size and composition, this partitioning can alter radiative properties and impact cloud activation processes. We present measurements and model predictions on how activity and pH influence the evaporation of SVOCs from particles to the gas phase, specifically investigating aqueous inorganic particles containing dicarboxylic acids (DCAs). The aerosols are studied at the single-particle level by using optical trapping and cavity-enhanced Raman spectroscopy. Optical resonances in the spectra enable precise size tracking, while vibrational bands allow real-time monitoring of pH. Results are compared to a Maxwell-type model that accounts for volatile and nonvolatile solutes in aqueous droplets that are held at a constant relative humidity. The aerosol inorganic-organic mixture functional group activity coefficients thermodynamic model and Debye-Hückel theory are both used to calculate the activities of the species present in the droplet. For DCAs, we find that the evaporation rate is highly sensitive to the particle pH. For acidity changes of approximately 1.5 pH units, we observe a shift from a volatile system to one that is completely nonvolatile. We also observe that the pH itself is not constant during evaporation; it increases as DCAs evaporate, slowing the rate of evaporation until it eventually ceases. Whether a DCA evaporates or remains a stable component of the droplet is determined by the difference between the lowest p of the DCA and the pH of the droplet.
半挥发性有机化合物(SVOCs)在凝聚相和气相之间的分配对气溶胶粒子的性质有重要影响。除了影响大小和组成外,这种分配还可以改变辐射性质并影响云激活过程。我们展示了关于活性和 pH 值如何影响 SVOC 从粒子到气相蒸发的测量和模型预测,特别是研究了含有二羧酸(DCA)的水相无机粒子。通过使用光学捕获和腔增强拉曼光谱,在单粒子水平上研究了气溶胶。光谱中的光学共振使精确的尺寸跟踪成为可能,而振动带则允许实时监测 pH 值。结果与一个 Maxwell 型模型进行了比较,该模型考虑了在恒定相对湿度下保持的水相液滴中的挥发性和非挥发性溶质。气溶胶无机-有机混合物官能团活度系数热力学模型和 Debye-Hückel 理论都用于计算液滴中存在的物质的活度。对于 DCA,我们发现蒸发速率对颗粒 pH 值非常敏感。对于约 1.5 pH 单位的酸度变化,我们观察到从挥发性体系到完全非挥发性体系的转变。我们还观察到,在蒸发过程中 pH 值本身并不恒定;随着 DCA 的蒸发,pH 值会增加,从而减缓蒸发速率,直到最终停止。DCA 是蒸发还是仍然是液滴的稳定组成部分取决于 DCA 的最低 p 值与液滴的 pH 值之间的差异。