Abstract
AbstractSea salt aerosols (SSAs) often mix with organic matter via sea‐to‐air emission, photochemical oxidation, and atmospheric transport, which change particle hygroscopicity and real refractive index (RRI), thereby the radiative effects. However, the influence of water uptake and organic matters on radiative effects is not well understood. In this study, relative humidity (RH)‐dependent growth factor (GF), light scattering enhancement factor, RRI (nmea), and radiative forcing efficiency (RFE) in the visible spectrum of SSAs/malonic acid (MA) internally mixed aerosols were investigated. Our results showed that MA‐mediated SSAs readily absorbed water even at low RH but suppressed hygroscopic growth at high RH. The discrepancy between Zdanovskii‐Stokes‐Robinson predictions and measured GF indicated that the suppressing effect on size caused by produced malonate salts in chloride depletion became more evident as MA content increased. RRI in the visible spectrum decreased as MA got enriched and approached toward water's RRI at high RH, resulting in a less cooling effect. The increasing RH reduced RFE both by decreasing RRI and increasing particle size substantially. Ignoring the effect of MA on particle size and RRI under varied RH, errors in RFE at 525 nm up to 25% could be induced. Volume mixing rule performs well in predicting the RRI of mixed aerosols in dry conditions, while the retrieved difference of 0.061 between volume mixing RRI nvol and nmea would make the error in RFE up to 1.15 W·m−2·Aerosol optical depth−1 at 87% RH. Our study helps understand the impact of water content and dicarboxylic acids on the direct radiative effects of SSAs.
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