“…The organic material will then typically exist at the particle surface and can impede reactive processes such as uptake of N 2 O 5 (g), HNO 3 (g), or H 2 SO 4 (g) that drives particulate chloride displacement ,, to the gas phase as ClNO 2 (g) or HCl(g). These reactions will also alter particle hygroscopicity and water uptake, phase transitions, pH, and thus aqueous chemical reactions. ,,− Chloride displacement reactions are also significant because of the differing hygroscopic behavior, phase transitions, and solubilities of chloride and the nitrate, sulfate, or organic phases that form through these gas–particle reactions. , The effects of organic carbon particle coatings on gas reactive uptake depend on particle composition, the gas-phase reactant, and ambient atmospheric conditions such as relative humidity that control phase transitions, particle phase, and water content. ,,− For example, our prior measurements of N 2 O 5 reactive uptake and ClNO 2 formation from BBA observed low and inconsistent yields and postulated this could be related to particle morphology or phase state. , Our recent experiments where the BBA was exposed to higher relative humidities above typical salt deliquescence points prior to exposure to N 2 O 5 confirmed that chloride reactivity in BBA can be impeded by organic coatings and solid and thus less reactive effloresced chloride phases …”