A platform for research: civil engineering, architecture and urbanism
Heterogeneous reactions of ozone with pyrene, 1-hydroxypyrene and 1-nitropyrene adsorbed on particles
AbstractThis work deals with the kinetic study of the reactions of ozone with pyrene, 1-hydroxypyrene and 1-nitropyrene, adsorbed on model particles. Experiments were performed at room temperature and atmospheric pressure, using a quasi-static flow reactor in the absence of light. Compounds were extracted from particles using pressurized 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 O3 concentrations from which second order rate constants were calculated. The following rate constant values were obtained at 293 K: k(O3 + Pyrene) = (3.2 ± 0.7) × 10−16 cm3 molecule−1 s−1; k(O3 + 1OHP) = (7.7 ± 1.4) ×10 −16 cm3 molecule−1 s−1; and k(O3 + 1NP) = (2.2 ± 0.5) × 10−17 cm3 molecule−1 s−1, for pyrene, 1-hydroxypyrene and 1-nitropyrene adsorbed on silica particles. The variation in the rate constants demonstrates the strong influence of the substituent (OH or NO2) on the heterogeneous reactivity of pyrene. The pyrene particulate concentration was also varied in order to check how this parameter may influence the experiments. Finally, oxidation products were investigated for all reactions and some were detected and identified for the first time for ozone heterogeneous reaction with pyrene adsorbed on particles.
Heterogeneous reactions of ozone with pyrene, 1-hydroxypyrene and 1-nitropyrene adsorbed on particles
AbstractThis work deals with the kinetic study of the reactions of ozone with pyrene, 1-hydroxypyrene and 1-nitropyrene, adsorbed on model particles. Experiments were performed at room temperature and atmospheric pressure, using a quasi-static flow reactor in the absence of light. Compounds were extracted from particles using pressurized 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 O3 concentrations from which second order rate constants were calculated. The following rate constant values were obtained at 293 K: k(O3 + Pyrene) = (3.2 ± 0.7) × 10−16 cm3 molecule−1 s−1; k(O3 + 1OHP) = (7.7 ± 1.4) ×10 −16 cm3 molecule−1 s−1; and k(O3 + 1NP) = (2.2 ± 0.5) × 10−17 cm3 molecule−1 s−1, for pyrene, 1-hydroxypyrene and 1-nitropyrene adsorbed on silica particles. The variation in the rate constants demonstrates the strong influence of the substituent (OH or NO2) on the heterogeneous reactivity of pyrene. The pyrene particulate concentration was also varied in order to check how this parameter may influence the experiments. Finally, oxidation products were investigated for all reactions and some were detected and identified for the first time for ozone heterogeneous reaction with pyrene adsorbed on particles.
Heterogeneous reactions of ozone with pyrene, 1-hydroxypyrene and 1-nitropyrene adsorbed on particles
Miet, K. (author) / Le Menach, K. (author) / Flaud, P.M. (author) / Budzinski, H. (author) / Villenave, E. (author)
Atmospheric Environment ; 43 ; 3699-3707
2009-04-16
9 pages
Article (Journal)
Electronic Resource
English
PAH , Pyrene , 1-Hydroxypyrene , 1-Nitropyrene , Silica particles , Ozone , Oxidation products , Kinetics
British Library Online Contents | 1998
|Homogeneous and heterogeneous reactions of phenanthrene with ozone
Elsevier | 2009
|