Heterogeneous reactivity of pyrene and 1-nitropyrene with NO2: Kinetics,product yields and mechanism |
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| Authors: | K Miet K Le Menach P-M Flaud H Budzinski E Villenave |
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| Institution: | 1. Université de Bordeaux, Institut des Sciences Moléculaires, Laboratoire de Physico et Toxico Chimie de l''Environnement, 33405 Talence cedex, France;2. CNRS, UMR 5255, 33405 Talence cedex, France;1. Department of Earth and Environmental Sciences, University of Milano-Bicocca, P.zza della Scienza 1, 20126 Milan, Italy;2. Institute of Atmospheric Sciences and Climate (ISAC), Italian National Research Council (CNR), Via Gobetti 101, 40129 Bologna, Italy;3. INNOVHUB–SSI, Divisione Stazione Sperimentale per i Combustibili, Via Galileo Galilei 1, 20097 San Donato Milanese, MI, Italy;1. Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kakuma-machi, Kanazawa 920-1192, Japan;2. Ishikawa Prefectural Institute of Public Health and Environmental Science, 1-11, Taiyogaoka, Kanazawa 920-1154, Japan;3. Graduate School of Energy Science, Kyoto University, Gokasho, Uji 611-0011, Japan;1. Key Laboratory of Songliao Aquatic Environment (Jilin Jianzhu University), Ministry of Education, Changchun, 130118, China;2. Key Laboratory of Groundwater Resources and Environment (Jilin University), Ministry of Education, Changchun, 130021, China |
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| Abstract: | The heterogeneous reactivity of nitrogen dioxide with pyrene and 1-nitropyrene (1NP) adsorbed on silica particles has been investigated using a fast-flow-tube in the absence of light. Reactants and products were extracted from particles using pressurised fluid extraction (PFE) and concentration measurements were performed using gas chromatography/mass spectrometry (GC/MS). The pseudo-first order rate constants were obtained from the fit of the experimental decay of particulate polycyclic compound concentrations versus reaction time. Experiments were performed at three different NO2 concentrations and second order rate constants were calculated considering the oxidant concentration. The following rate constant values were obtained at room temperature: k(NO2 + pyrene) = (9.3 ± 2.3) × 10?17 cm3 molecule?1 s?1 and k(NO2 + 1NP) = (6.2 ± 1.5) × 10?18 cm3 molecule?1 s?1, showing that the reactivity of 1NP was slower by a factor of 15 than that of pyrene. 1NP was identified as the only NO2-initiated oxidation product of pyrene and all the three dinitropyrenes were identified in the case of the 1NP reaction. The product quantification allowed showing that the kinetics of oxidation product formation was equal to that measured for parent compounds degradation, within uncertainties, confirming the validity of the reaction kinetics measurements. |
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