Abstract

ABSTRACTHygroscopic growth factor (GF) distributions of 13, 25, 50, 100, 200, and 400 nm particles measured with a Hygroscopic Tandem Differential Mobility Analyzer (HTDMA) from 2009 to 2012 at the Southern Great Plains (SGP) site in Oklahoma, U.S. were used to describe time of day- and annually-averaged hygroscopicity parameters (κ). A diel pattern was often observed with an average daytime κ that was higher than that at other times, especially on days with new particle formation (NPF) events. The average hygroscopicity of the smaller and larger particles at the tails of the measured size range was higher than that in between, with the minimum for each of the 4 years at 50 nm. This pattern is thought to result in part from addition of soluble inorganic and organic compounds formed through gas phase and aqueous phase reactions for the smaller and larger particles, respectively. The size dependence is reflected in the averaged κ and in the frequency with which GF distributions possessed modes categorized as nearly-hydrophobic, less hygroscopic, and hygroscopic. A hygroscopicity-based mixing state parameter, MShyg, defined as the ratio of the standard deviation (SD) of a measured GF distribution to the size specific threshold SD roughly separating internal and external mixtures, was used to study the diel and seasonal variation in particle mixing state. Internal mixtures were found to be more common during the daytime and during the summer, likely reflecting more rapid photochemical processing and growth at those times.

Highlights

  • Atmospheric particles influence climate by scattering and absorbing solar radiation and by acting as cloud condensation nuclei (CCN)

  • The measured distribution of particle hygroscopicity is usually reported in terms of the hygroscopic growth factor or Growth Factor (GF), which is the ratio of the Mahish and Collins, Aerosol and Air Quality Research, 17: 1489–1500, 2017 diameter of a particle (D) at high relative humidity to its dry size (Dhigh RH/Ddry)

  • Diel Variation in Kappa (κ) The hygroscopicity parameter, κ, was determined for each mode in all GF distributions measured over the 4-year period

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Summary

Introduction

Atmospheric particles influence climate by scattering and absorbing solar radiation and by acting as cloud condensation nuclei (CCN) The extent of their influence depends on the size of the particles, which can be significantly increased for hygroscopic aerosols when exposed to high relative humidity (RH). Gasparini et al (2006) reported increased hygroscopicity with increasing particle size based on HTDMA measurements made in May 2003 at the Department of Energy’s (DOE) Southern Great Plains (SGP) Atmospheric Radiation Measurement (ARM) site in an agricultural area of Oklahoma, U.S, which is where the data reported here were collected This result is consistent with the findings of Holmgren et al (2014), Levin et al (2014), and others. An interpretation of this size dependent hygroscopicity is a higher organic content in smaller particles. Levin et al (2014) reported results from an elevation of 2300 m in Pike National Forest in the central Rocky Mountains of Colorado, U.S Their study support this interpretation, with higher organic fraction in smaller particles and increasing inorganic fraction in larger particles

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