用原位透射电子显微镜观察单个氯化钠纳米颗粒在潮解过程中的溶解动力学。

IF 11.3 1区 环境科学与生态学 Q1 ENGINEERING, ENVIRONMENTAL
环境科学与技术 Pub Date : 2024-09-03 Epub Date: 2024-08-19 DOI:10.1021/acs.est.4c02356
Yuhang Wang, Dewansh Rastogi, Kotiba A Malek, Jiayue Sun, Martin Changman Ahn, Akua A Asa-Awuku, Taylor J Woehl
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引用次数: 0

摘要

吸湿气溶胶粒子上的水蒸气凝结在云的形成、气候变化、二次气溶胶的形成和气溶胶老化中起着重要作用。传统认识认为,纳米级吸湿气溶胶粒子的潮解是一种近乎瞬时的固相到液相的转变。然而,由于缺乏高空间和时间分辨率的单颗粒测量方法,在潮解之前和潮解过程中水凝结和气溶胶颗粒溶解的纳米级动力学仍然模糊不清。在这里,我们利用对单个氯化钠(NaCl)纳米颗粒的实时原位透射电子显微镜(TEM)成像来证明,在潮解之前和潮解过程中的水吸附和气溶胶颗粒溶解是一个多步骤的动态过程。研究人员对实验室产生的氯化钠气溶胶进行了水凝结和气溶胶粒子溶解的研究,发现随着相对湿度(RH)的增加,水凝结和气溶胶粒子溶解分为三个不同的阶段。首先,一个小于 100 纳米的水层吸附在氯化钠立方体上,导致尖角溶解和截断。随着相对湿度的增加,水层增长到几百纳米,并迅速被溶质饱和,颗粒溶解停止就是证明。相邻的立方体角显示出第二尺度的曲率波动,但没有净颗粒溶解或水层厚度变化。我们认为,液滴溶质浓度的波动推动了氯化钠从局部高曲率区域向低曲率区域的迁移。最后,我们观察到液态水滴和气溶胶粒子在潮解前共存。颗粒沿着单一晶体学方向离散溶解,中间有几秒钟的滞后时间,没有溶解。这项研究表明,大小在 100 纳米到几微米范围内的简单纯盐颗粒的潮解并不是瞬时相变,而是涉及一系列复杂的溶解和水凝结动力学过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Imaging Dissolution Dynamics of Individual NaCl Nanoparticles during Deliquescence with <i>In Situ</i> Transmission Electron Microscopy.

Imaging Dissolution Dynamics of Individual NaCl Nanoparticles during Deliquescence with In Situ Transmission Electron Microscopy.

Water vapor condensation on hygroscopic aerosol particles plays an important role in cloud formation, climate change, secondary aerosol formation, and aerosol aging. Conventional understanding considers deliquescence of nanosized hygroscopic aerosol particles a nearly instantaneous solid to liquid phase transition. However, the nanoscale dynamics of water condensation and aerosol particle dissolution prior to and during deliquescence remain obscure due to a lack of high spatial and temporal resolution single particle measurements. Here we use real time in situ transmission electron microscopy (TEM) imaging of individual sodium chloride (NaCl) nanoparticles to demonstrate that water adsorption and aerosol particle dissolution prior to and during deliquescence is a multistep dynamic process. Water condensation and aerosol particle dissolution was investigated for lab generated NaCl aerosols and found to occur in three distinct stages as a function of increasing relative humidity (RH). First, a < 100 nm water layer adsorbed on the NaCl cubes and caused sharp corners to dissolve and truncate. The water layer grew to several hundred nanometers with increasing RH and was rapidly saturated with solute, as evidenced by halting of particle dissolution. Adjacent cube corners displayed second-scale curvature fluctuations with no net particle dissolution or water layer thickness change. We propose that droplet solute concentration fluctuations drove NaCl transport from regions of high local curvature to regions of low curvature. Finally, we observed coexistence of a liquid water droplet and aerosol particle immediately prior to deliquescence. Particles dissolved discretely along single crystallographic directions, separated by few second lag times with no dissolution. This work demonstrates that deliquescence of simple pure salt particles with sizes in the range of 100 nm to several microns is not an instantaneous phase transition and instead involves a range of complex dissolution and water condensation dynamics.

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来源期刊
环境科学与技术
环境科学与技术 环境科学-工程:环境
CiteScore
17.50
自引率
9.60%
发文量
12359
审稿时长
2.8 months
期刊介绍: Environmental Science & Technology (ES&T) is a co-sponsored academic and technical magazine by the Hubei Provincial Environmental Protection Bureau and the Hubei Provincial Academy of Environmental Sciences. Environmental Science & Technology (ES&T) holds the status of Chinese core journals, scientific papers source journals of China, Chinese Science Citation Database source journals, and Chinese Academic Journal Comprehensive Evaluation Database source journals. This publication focuses on the academic field of environmental protection, featuring articles related to environmental protection and technical advancements.
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