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The gas-phase reaction of naphthalene with N2O5 to form nitronaphthalenes
Affiliation:1. Department of Computer Science and Engineering, Institute of Technical Education and Research, Siksha ‘O’ Anusandhan (Deemed to be) University, Bhubaneswar, Odisha, India;2. Department of Computer Application, Institute of Technical Education and Research, Siksha ‘O’ Anusandhan (Deemed to be) University, Bhubaneswar, Odisha, India;3. Department of Electrical and Electronics Engineering, Institute of Technical Education and Research, Siksha ‘O’ Anusandhan (Deemed to be) University, Bhubaneswar, Odisha, India;4. School of Science and Technology, Nottingham Trent University, Nottingham, United Kingdom;5. Faculty of Communication Sciences, University of Teramo, Teramo, Italy;1. Department of Chemical Engineering and Biotechnology, University of Cambridge, West Cambridge Site, Philippa Fawcett Drive, Cambridge CB3 0AS, United Kingdom;2. CARES, Cambridge Centre for Advanced Research and Education in Singapore, 1 Create Way, CREATE Tower, #05-05, 138602, Singapore;3. School of Chemical and Biomedical Engineering, Nanyang Technological University, 62 Nanyang Drive, 637459, Singapore
Abstract:While the formation of nitroarenes from the reaction of NO2, containing traces of HNO3, in air with polycyclic aromatic hydrocarbons (PAH) adsorbed on combustion generated particles is now well recognized, little is known about the gas-phase reactions of PAH. In this study, the gas-phase reactions in air of N2O3 with part-per-million levels of naphthalene have been studied at room temperature and atmospheric pressure in a 5800V Teflon-coated environmental chamber. The kinetic data obtained showed that in these N2O5-NO3-NO2-air mixtures studied, naphthalene did not react with the NO3 radical at an observable rate, but that it reacted with N2O5 with a rate constant of ~ (2–3) × 10−17 cm3 molecule−1 s−1. Significant yields of 1-nitronaphthalene and 2-nitronaphthalene ( ~ 18 and ~ 7.5%, respectively) were obtained from this reaction. The latter is a procarcinogen capable of being metabolized in animals to the carcinogen β-naphthylamine. These results and their atmospheric implications are discussed.
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