Abstract. Secondary organic aerosol (SOA) is of great importance, affecting human health and the prediction of climate change; however, the factors (e.g., temperature, acidity of pre-existing particles, and oxidants) influencing its formation are not sufficiently resolved. In this study, a compact Teflon atmospheric simulation chamber is developed, in which reactions in atmospheric pressure conditions can be performed with controlled temperature, humidity, oxidation agents, and seed particle acidity. Using the chamber, α-pinene ozonolysis SOA formation was simulated under temperatures of 278 K, 288 K, and 298 K with neutral/acidic seed aerosols. The SOA components of m / z less than 400 were analyzed using negative electrospray ionization liquid-chromatography time-of-flight mass spectrometry. The temperature and acidity dependence of SOA yields and chemical components were investigated. From the slightly negative temperature dependence of the SOA yields, the enthalpy of vaporization in neutral and acidic seed conditions was estimated to be 25 and 44 kJ mol−1, respectively. With these values, the volatility distributions of the identified SOA compounds were consistently explained. Acidity dependence analysis of the chemical formula, molecular mass, and O : C ratio of the detected compounds indicated the enhanced formation of many oligomers in the wide molecular mass range with a wide range of O : C ratios under acidic seed conditions. The acidity dependence of certain major compounds could be explained by acid-catalyzed heterogeneous reactions (e.g., m / z 171, 185, 343, and 357) or acid-catalyzed decomposition of hydroperoxides (e.g., m / z 215 and 197). In addition, the formation of organosulfates (OS) was observed under acidic seed conditions. We proposed that six of the eleven detected OS were possibly formed through the aldehyde + HSO4− pathway. Further studies on the OS formation during α-pinene ozonolysis are warranted.