A novel methodology for assessing the hygroscopicity of aerosol filter samples

<p>Due to US regulations, concentrations of hygroscopic inorganic sulfate and nitrate have declined in recent years, leading to an increased importance of the hygroscopic nature of organic matter (OM). The hygroscopicity of OM is poorly characterized because only a fraction of the multitude of...

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Main Authors: N. Raparthi, A. S. Wexler, A. M. Dillner
Format: Article
Language:English
Published: Copernicus Publications 2025-02-01
Series:Atmospheric Measurement Techniques
Online Access:https://amt.copernicus.org/articles/18/603/2025/amt-18-603-2025.pdf
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author N. Raparthi
A. S. Wexler
A. S. Wexler
A. S. Wexler
A. S. Wexler
A. M. Dillner
author_facet N. Raparthi
A. S. Wexler
A. S. Wexler
A. S. Wexler
A. S. Wexler
A. M. Dillner
author_sort N. Raparthi
collection DOAJ
description <p>Due to US regulations, concentrations of hygroscopic inorganic sulfate and nitrate have declined in recent years, leading to an increased importance of the hygroscopic nature of organic matter (OM). The hygroscopicity of OM is poorly characterized because only a fraction of the multitude of organic compounds in the atmosphere is readily measured, and there is limited information on their hygroscopic behaviors. Hygroscopicity of aerosol is traditionally measured using a humidified tandem differential mobility analyzer (HTDMA) or electrodynamic balance (EDB). EDB measures water uptake by a single particle. For ambient and chamber studies, HTDMA measurements provide water uptake and particle size information but not chemical composition. To fill this information gap, we developed a novel methodology to assess the water uptake by particles collected on Teflon filters. This method uses the same filter sample for both hygroscopicity measurements and chemical characterization, thereby providing an opportunity to link the measured hygroscopicity with ambient particle composition. To test the method, hygroscopic measurements were conducted in the laboratory for ammonium sulfate, sodium chloride, glucose, and malonic acid, which were collected on 25 mm Teflon filters using an aerosol generator and sampler. Constant-humidity solutions (CHSs), including potassium chloride, barium chloride dihydrate, and potassium sulfate, were employed in a saturated form to maintain the relative humidity (RH) at approximately 84 %, 90 %, and 97 % in small chambers. Our preliminary experiments revealed that, without the pouch, water uptake measurements were not feasible due to rapid water loss during weighing. Additionally, we observed some absorption by the aluminum pouch itself. To account for this, concurrent measurements were conducted for both the loaded and the blank filters at each RH level. Thus, the dry loaded and blank Teflon filters were placed in aluminum pouches with one side open and in RH-controlled chambers for more than 24 h. The wet loaded samples and wet blanks were then weighed using an ultramicrobalance to determine the water uptake by the respective compound and the blank Teflon filter. The net amount of water absorbed by each compound was calculated by subtracting the water uptake of the blank filter from that of the wet loaded filter. Hygroscopic parameters, including the water-to-solute (W <span class="inline-formula"><math xmlns="http://www.w3.org/1998/Math/MathML" id="M1" display="inline" overflow="scroll" dspmath="mathml"><mo>/</mo></math><span><svg:svg xmlns:svg="http://www.w3.org/2000/svg" width="8pt" height="14pt" class="svg-formula" dspmath="mathimg" md5hash="1b4178c77ca0d4bfee6c9ddd864f3a43"><svg:image xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="amt-18-603-2025-ie00001.svg" width="8pt" height="14pt" src="amt-18-603-2025-ie00001.png"/></svg:svg></span></span> S) ratio, molality, mass fraction solute (mfs), and growth factors (GFs), were calculated from the measurements. The results obtained are consistent with those reported by the Extended Aerosol Inorganics Model (E-AIM) and previous studies utilizing HTDMA and EDB for these compounds, highlighting the accuracy of this new methodology. This new approach enables the hygroscopicity and chemical composition of individual filter samples to be assessed so that in complex mixtures, such as chamber and ambient samples, the total water uptake can be parsed between the inorganic and organic components of the aerosol.</p>
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spelling doaj-art-b2cbca75e62a4db2a44898ecb03e4e462025-02-03T14:13:15ZengCopernicus PublicationsAtmospheric Measurement Techniques1867-13811867-85482025-02-011860361810.5194/amt-18-603-2025A novel methodology for assessing the hygroscopicity of aerosol filter samplesN. Raparthi0A. S. Wexler1A. S. Wexler2A. S. Wexler3A. S. Wexler4A. M. Dillner5Air Quality Research Center, University of California, Davis, CA 95618, USAAir Quality Research Center, University of California, Davis, CA 95618, USAMechanical and Aerospace Engineering, University of California, Davis, CA 95616, USACivil and Environmental Engineering, University of California, Davis, CA 95616, USALand, Air and Water Resources, University of California, Davis, CA 95616, USAAir Quality Research Center, University of California, Davis, CA 95618, USA<p>Due to US regulations, concentrations of hygroscopic inorganic sulfate and nitrate have declined in recent years, leading to an increased importance of the hygroscopic nature of organic matter (OM). The hygroscopicity of OM is poorly characterized because only a fraction of the multitude of organic compounds in the atmosphere is readily measured, and there is limited information on their hygroscopic behaviors. Hygroscopicity of aerosol is traditionally measured using a humidified tandem differential mobility analyzer (HTDMA) or electrodynamic balance (EDB). EDB measures water uptake by a single particle. For ambient and chamber studies, HTDMA measurements provide water uptake and particle size information but not chemical composition. To fill this information gap, we developed a novel methodology to assess the water uptake by particles collected on Teflon filters. This method uses the same filter sample for both hygroscopicity measurements and chemical characterization, thereby providing an opportunity to link the measured hygroscopicity with ambient particle composition. To test the method, hygroscopic measurements were conducted in the laboratory for ammonium sulfate, sodium chloride, glucose, and malonic acid, which were collected on 25 mm Teflon filters using an aerosol generator and sampler. Constant-humidity solutions (CHSs), including potassium chloride, barium chloride dihydrate, and potassium sulfate, were employed in a saturated form to maintain the relative humidity (RH) at approximately 84 %, 90 %, and 97 % in small chambers. Our preliminary experiments revealed that, without the pouch, water uptake measurements were not feasible due to rapid water loss during weighing. Additionally, we observed some absorption by the aluminum pouch itself. To account for this, concurrent measurements were conducted for both the loaded and the blank filters at each RH level. Thus, the dry loaded and blank Teflon filters were placed in aluminum pouches with one side open and in RH-controlled chambers for more than 24 h. The wet loaded samples and wet blanks were then weighed using an ultramicrobalance to determine the water uptake by the respective compound and the blank Teflon filter. The net amount of water absorbed by each compound was calculated by subtracting the water uptake of the blank filter from that of the wet loaded filter. Hygroscopic parameters, including the water-to-solute (W <span class="inline-formula"><math xmlns="http://www.w3.org/1998/Math/MathML" id="M1" display="inline" overflow="scroll" dspmath="mathml"><mo>/</mo></math><span><svg:svg xmlns:svg="http://www.w3.org/2000/svg" width="8pt" height="14pt" class="svg-formula" dspmath="mathimg" md5hash="1b4178c77ca0d4bfee6c9ddd864f3a43"><svg:image xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="amt-18-603-2025-ie00001.svg" width="8pt" height="14pt" src="amt-18-603-2025-ie00001.png"/></svg:svg></span></span> S) ratio, molality, mass fraction solute (mfs), and growth factors (GFs), were calculated from the measurements. The results obtained are consistent with those reported by the Extended Aerosol Inorganics Model (E-AIM) and previous studies utilizing HTDMA and EDB for these compounds, highlighting the accuracy of this new methodology. This new approach enables the hygroscopicity and chemical composition of individual filter samples to be assessed so that in complex mixtures, such as chamber and ambient samples, the total water uptake can be parsed between the inorganic and organic components of the aerosol.</p>https://amt.copernicus.org/articles/18/603/2025/amt-18-603-2025.pdf
spellingShingle N. Raparthi
A. S. Wexler
A. S. Wexler
A. S. Wexler
A. S. Wexler
A. M. Dillner
A novel methodology for assessing the hygroscopicity of aerosol filter samples
Atmospheric Measurement Techniques
title A novel methodology for assessing the hygroscopicity of aerosol filter samples
title_full A novel methodology for assessing the hygroscopicity of aerosol filter samples
title_fullStr A novel methodology for assessing the hygroscopicity of aerosol filter samples
title_full_unstemmed A novel methodology for assessing the hygroscopicity of aerosol filter samples
title_short A novel methodology for assessing the hygroscopicity of aerosol filter samples
title_sort novel methodology for assessing the hygroscopicity of aerosol filter samples
url https://amt.copernicus.org/articles/18/603/2025/amt-18-603-2025.pdf
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