FORMATION OF NITROARENES FROM THE REACTION OF POLYCYCLIC AROMATIC-HYDROCARBONS WITH DINITROGEN PENTAOXIDE
FORMATION OF NITROARENES FROM THE REACTION OF POLYCYCLIC AROMATIC-HYDROCARBONS WITH DINITROGEN PENTAOXIDE
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DOI:
10.1021/es00141a017
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发表时间:
1985-01-01
影响因子:
11.4
通讯作者:
HARGER, WP
中科院分区:
文献类型:
--
作者:
PITTS, JN;SWEETMAN, JA;HARGER, WP
Reactions of six polycyclic aromatic hydrocarbons (PAH) [fluoranthene (FL), pyrene (PY), benz[a]-anthracene (BaA), chrysene (CHRY), benzo[a]pyrene (BaP), and perylene (PER)], deposited on glass-fiber filters, with gaseous N2O5 in air were investigated in an all-Teflon chamber. Pyrene, FL, BaP, and BaA gave significant yields of nitro derivatives after only a 30-min exposure. In control exposures to NO2 plus HNO3 mixtures or to HNO3 alone, the yields of nitro derivatives of PY, FL, and BaA were very low relative to those in the N2O5 exposures. The reactivity ranking of these PAH toward gaseous N2O5 was PY > FL > BaP > BaA > PER > CHRY. This order is significantly different from that previously observed for nitration of PAH depositied on glass-fiber filters and exposed to a flow of gaseous NO2 + HNO3 or for nitration of PAH in solution by NO2/N2O4 mixtures. It also differs from the reactivity ranking determined in this study for the reaction of these PAH with N2O5 in CCl4 solution of PER > BaP > BaA .gtoreq. PY > FL .gtoreq. CHRY. Environmental implications are disscussed.