Abstract. Gas-phase oxidation pathways and products of anthropogenic volatile organic compounds (VOCs), mainly aromatics, are the subject of intensive research with attention paid to their contributions to secondary organic aerosol (SOA) formation and potentially, new particle formation (NPF) in the urban atmosphere. In this study, a series of OH-initiated oxidation experiments of trimethylbenzene (TMB, C9H12) including 1,2,4-TMB, 1,3,5-TMB, 1,2,3-TMB, and 1,2,4-(methyl-D3)-TMBs (C9H9D3) were investigated in an oxidation flow reactor (OFR), in the absence and presence of NOx. Products were measured using a suite of state-of-the-art instruments, i.e., a nitrate-based chemical ionization – atmospheric pressure interface time-of-flight mass spectrometer (Nitrate CI-APi-TOF), an iodide-adduct chemical ionization – time-of-flight mass spectrometer (Iodide CI-TOF) equipped with a Filter Inlet for Gases and AEROsols (FIGAERO), and a Vocus proton-transfer-reaction mass spectrometer (Vocus PTR). A large number of C9 products with 1–11 oxygen atoms and C18 products presumably formed from dimerization of C9 peroxy radicals were observed, hinting the extensive existence of autoxidation and accretion reaction pathways in the OH-initiated oxidation reactions of TMBs. Oxidation products of 1,2,4-(methyl-D3)-TMBs with deuterium atoms in different methyl substituents were then used as a molecular basis to propose potential autoxidation reaction pathways. Accretion of C9 peroxy radicals is the most significant for aromatics with meta-substituents and the least for aromatics with ortho-substituents, if the number and size of substituted groups are identical. The presence of NOx would suppress the formation of C18 highly oxygenated molecules (HOMs) and enhance the formation of organonitrates, and even dinitrate organic compounds. Our results show that the oxidation products of TMB are much more diverse and could be more oxygenated than the current mechanisms predict.
Theoretical study on the reaction mechanism of “ligandless” Ni-catalyzed hydrodesulfurization of aryl sulfide
