Physical and chemical properties of aerosol particles and cloud residuals on Mt. Åreskutan in Central Sweden during summer 2014

E. Graham, P. Zieger, C. Mohr, U. Wideqvist, T. Hennig, A. Ekman, R. Krejci, J. Ström, I. Riipinen
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引用次数: 6

Abstract

Abstract The size distribution, volatility and hygroscopicity of ambient aerosols and cloud residuals were measured with a differential mobility particle sizer (DMPS) and a volatility–hygroscopicity tandem differential mobility analyser (VHTDMA) coupled to a counterflow virtual impactor (CVI) inlet during the Cloud and Aerosol Experiment at Åre (CAEsAR) campaign at Mt. Åreskutan during summer 2014. The chemical composition of particulate matter (PM) and cloud water were analysed offline using thermo-optical OC/EC analysis and ion chromatography. The importance of aerosol particle size for cloud droplet activation and subsequent particle scavenging was clearly visible in the measured size distributions. Cloud residuals were shifted towards larger sizes compared to ambient aerosol, and the cloud events were followed by a size distribution dominated by smaller particles. Organics dominated both PM (62% organic mass fraction) and cloud water (63% organic mass fraction) composition. The volatility and hygroscopicity of the ambient aerosols were representative of homogeneous aged aerosol with contributions from biogenic secondary organics, with median volume fraction remaining (VFR) of 0.04–0.05, and median hygroscopicity parameter κ of 0.16–0.24 for 100–300 nm particles. The corresponding VFR and κ for the cloud residuals were 0.03–0.04 and 0.18–0.20. The chemical composition, hygroscopicity and volatility measurements thus showed no major differences between the ambient aerosol particles and cloud residuals. The VFR and κ values predicted based on the chemical composition measurements agreed well with the VHTDMA measurements, indicating the bulk chemical composition to be a reasonable approximation throughout the size distribution. There were indications, however, of some more subtle changes in time scales not achievable by the offline chemical analysis applied here. Further, online observations of aerosol and cloud residual chemical composition are therefore warranted.
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2014年夏季瑞典中部Åreskutan山上气溶胶粒子和云残留物的物理和化学性质
2014年夏季,在Åreskutan山Åre (CAEsAR)项目的云和气溶胶实验中,采用差分迁移率粒径仪(DMPS)和挥发性-吸湿性串联差分迁移率分析仪(VHTDMA)耦合逆流虚拟冲击器(CVI)入口,测量了环境气溶胶和云残留物的粒径分布、挥发性和吸湿性。采用热光学OC/EC分析和离子色谱法对云水和颗粒物的化学成分进行了离线分析。气溶胶粒径对云滴活化和随后的颗粒清除的重要性在测量的粒径分布中清晰可见。与环境气溶胶相比,云残余物的尺寸更大,云事件之后的尺寸分布以较小的颗粒为主。有机物在PM(62%有机质量分数)和云水(63%有机质量分数)组成中占主导地位。环境气溶胶的挥发性和吸湿性是由次生有机物贡献的均匀老化气溶胶的代表,100-300 nm颗粒的中位体积分数(VFR)为0.04-0.05,中位吸湿参数κ为0.16-0.24。云残差对应的VFR和κ分别为0.03 ~ 0.04和0.18 ~ 0.20。因此,化学成分、吸湿性和挥发性测量结果表明,环境气溶胶颗粒和云残留物之间没有重大差异。基于化学成分测量预测的VFR和κ值与VHTDMA测量结果吻合良好,表明总体化学成分在整个尺寸分布中是一个合理的近似值。然而,有迹象表明,在时间尺度上有一些更微妙的变化,这是这里应用的离线化学分析无法实现的。此外,在线观测气溶胶和云的残余化学成分是有必要的。
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