Observational analysis reveals aerosol acidity shifts with temperature and chemical precursors in fine particulate matter, highlighting key drivers of atmospheric pollution chemistry.
Aerosol acidity significantly affects atmospheric chemistry and human health, yet its driving factors remain controversial. This study systematically examined a year-long characteristics of water-soluble inorganic ions in PM2.5 in the semi-arid Guanzhong Plain, Northwest China, and quantitatively analyzed its acidity and driving factors. The annual mean pH of PM2.5 was 3.8 ± 1.0 (winter > spring > summer > autumn). As pollution increased, aerosol pH shifted from the acidic range (2–5) on clean days to a near-neutral range (3–6) on polluted days. Sensitivity tests and driver analysis revealed that atmospheric temperature (22.3 %–33.8 %), NHx (gas NH3+NH4+, 11.4 %–44.9 %), and SO42- (8.5 %–10.8 %) were common key factors influencing pH across all seasons, with the percentages representing the quantitative contribution of each factor to the overall pH variation. Among these, temperature played a dominant role in seasonal variations, while NHx was the primary contributor during autumn and winter. Notably, Ca2+ emerged as a unique driver specific to spring, the relative standard deviation (RSD) was 8.8 %, indicating a substantial impact of Ca2+ variability on spring aerosol pH. Relative humidity (RH) exhibited a distinctive non-linear regulatory effect, i.e., aerosol pH initially decreases and subsequently increases with rising RH (inflection point occurred at 60 %–85 %). This phenomenon is primarily attributed to an abrupt change in liquid water content triggered by the deliquescence of hygroscopic components. Our results enhance the understanding of the contributions of various factors to aerosol pH.
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Wang et al. (2026) studied this question.
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