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水合作用和化学老化过程中气溶胶颗粒粘度变化的直接成像。

Direct imaging of changes in aerosol particle viscosity upon hydration and chemical aging.

作者信息

Hosny N A, Fitzgerald C, Vyšniauskas A, Athanasiadis A, Berkemeier T, Uygur N, Pöschl U, Shiraiwa M, Kalberer M, Pope F D, Kuimova M K

机构信息

Department of Chemistry , Imperial College London , London , SW7 2AZ , UK . Email:

Department of Chemistry , University of Cambridge , Cambridge , CB2 1EW , UK . Email:

出版信息

Chem Sci. 2016 Feb 1;7(2):1357-1367. doi: 10.1039/c5sc02959g. Epub 2015 Nov 12.

Abstract

Organic aerosol particles (OA) play major roles in atmospheric chemistry, climate, and public health. Aerosol particle viscosity is highly important since it can determine the ability of chemical species such as oxidants, organics or water to diffuse into the particle bulk. Recent measurements indicate that OA may be present in highly viscous states, however, diffusion rates of small molecules such as water are not limited by these high viscosities. Direct observational evidence of kinetic barriers caused by high viscosity and low diffusivity in aerosol particles were not available until recently; and techniques that are able to dynamically quantify and track viscosity changes during atmospherically relevant processes are still unavailable for atmospheric aerosols. Here we report quantitative, real-time, online observations of microscopic viscosity changes in aerosol particles of atmospherically relevant composition, using fluorescence lifetime imaging (FLIM) of viscosity. We show that microviscosity in ozonated oleic acid droplets and secondary organic aerosol (SOA) particles formed by ozonolysis of myrcene increases substantially with decreasing humidity and atmospheric oxidative aging processes. Furthermore, we found unexpected heterogeneities of microviscosity inside individual aerosol particles. The results of this study enhance our understanding of organic aerosol processes on microscopic scales and may have important implications for the modeling of atmospheric aerosol growth, composition and interactions with trace gases and clouds.

摘要

有机气溶胶颗粒(OA)在大气化学、气候和公共卫生方面发挥着重要作用。气溶胶颗粒的粘度非常重要,因为它可以决定诸如氧化剂、有机物或水等化学物质扩散到颗粒内部的能力。最近的测量表明,OA可能以高粘性状态存在,然而,诸如水等小分子的扩散速率并不受这些高粘度的限制。直到最近才获得气溶胶颗粒中由高粘度和低扩散率导致的动力学障碍的直接观测证据;并且对于大气气溶胶,能够动态量化和跟踪与大气相关过程中粘度变化的技术仍然不可用。在此,我们使用粘度的荧光寿命成像(FLIM)报告了对具有大气相关组成的气溶胶颗粒微观粘度变化的定量、实时、在线观测。我们表明,臭氧化油酸液滴和由月桂烯臭氧化形成的二次有机气溶胶(SOA)颗粒中的微观粘度随着湿度降低和大气氧化老化过程而大幅增加。此外,我们发现单个气溶胶颗粒内部微观粘度存在意想不到的不均匀性。这项研究的结果增进了我们对微观尺度上有机气溶胶过程的理解,并且可能对大气气溶胶生长、组成以及与痕量气体和云相互作用的建模具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/53e1/5975791/ded8f06de011/c5sc02959g-f1.jpg

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