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Please use this identifier to cite or link to this item: https://shodhratna.thapar.edu:8443/jspui/handle/tiet/197
Title: Hygroscopic Properties of Water-Soluble Counterpart of Ultrafine Particles from Agriculture Crop-Residue Burning in Patiala, Northwestern India
Authors: Alang, Ashmeet Kaur
Aggarwal, Shankar G.
Singh, Khem
Johri, Prabha
Agarwal, Ravinder
Kawamura, Kimitaka
Keywords: aerosol size-resolved hygroscopicity; crop-residue burning aerosols; hygroscopic tandem differential mobility analyzer; aerosol water content
Issue Date: 2024
Publisher: Multidisciplinary Digital Publishing Institute (MDPI)
Abstract: What are the main findings? What is the implication of main findings? Hygroscopicity was primarily governed by inorganic fractions in particles; The abundance of individual constituent ionic species was highly responsible for aerosol water uptake. Highlights: To determine the link between hygroscopicity and the constituent chemical composition of real biomass-burning atmospheric particles, we collected and analyzed aerosols during wheat-straw (April–May), rice-straw (October–November), and no-burning periods (August–September) in 2008 and 2009 in Patiala, Punjab. A hygroscopicity tandem differential mobility analyzer (HTDMA) system was used to measure hygroscopicity at ~5 to ~95% relative humidity (RH) of aerosolized 100 nm particles generated from the water extracts of PM0.4 burning and no-burning aerosol samples. The chemical analyses of the extracts show that organic carbon and water-soluble inorganic-ion concentrations are 2 to 3 times higher in crop-residue burning aerosol samples compared to no-burning aerosols, suggesting the substantial contribution of biomass burning to the carbonaceous aerosols at the sampling site. We observed that aerosolized 100 nm particles collected during the crop-residue burning period show higher and more variable hygroscopic growth factor (g(RH)) ranging from 1.21 to 1.68 at 85% RH, compared to no-burning samples (1.27 to 1.33). Interestingly, crop-residue burning particles also show considerable shrinkage in their size (i.e., g(RH) < 1) at lower RH (<50%) in the dehumidification mode. The increased level of major inorganic ions in biomass-burning period aerosols is a possible reason for higher g(RH) as well as the observed particle shrinkage. Overall, the measured g(RH), together with the correlation observed between aerosol water content and ionic-species volume fraction, and the study of the abundance of individual constituent ionic species suggests that inorganic salts and their proportion in aerosol particles primarily governed the aerosol hygroscopicity. © 2024 by the authors.
URI: https://shodhratna.thapar.edu:8443/jspui/handle/tiet/197
ISSN: 20734433
Appears in Collections:EE Journal Articles

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