Evidence for destruction of PCBs by the OH radical in urban atmospheres

被引:53
作者
Totten, LA [1 ]
Eisenreich, SJ [1 ]
Brunciak, PA [1 ]
机构
[1] Rutgers State Univ, Dept Environm Sci, New Brunswick, NJ 08901 USA
基金
美国海洋和大气管理局;
关键词
oxidation; degradation; diurnal variation; homologue groups;
D O I
10.1016/S0045-6535(01)00326-5
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Evidence for reaction of polychlorinated biphenyl (PCB) congeners with the hydroxyl (OH) radical in the troposphere was observed in diurnal variations in ambient gas-phase PCB concentrations at three urban sampling sites located in the Chicago, IL; Baltimore, MD; and Jersey City, NJ urban/industrial areas. The magnitude of the depletion of individual PCB congeners decreased by about 10-20% for each additional chlorine substituent, reflecting slower reaction rates for higher MW congeners with the OH radical. Octa-and nonachlorobiphenyls, which are largely unreactive with the OH radical, were used as tracers to investigate the effects of dilution on diurnal variation. The environmental rate constants for disappearance of the PCBs range from about 1.0 day(-1) for trichlorobiphenyls to about 0.3 day(-1) for hexachlorobiphenyls. Assuming a OH radical concentration of 3 x 10(6) molecules cm(-3), the second-order rate constants for reaction of specific congeners with the OH radical are consistent with laboratory measurements. More importantly, the relative reactivity of PCB homologues agrees well with the relationship predicted by other researchers from laboratory measurements, suggesting that losses of PCBs during daytime tropospheric transport are due at least in part to reactions with the CH radical. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:735 / 746
页数:12
相关论文
共 60 条
[1]   OH radical reactions: The major removal pathway for polychlorinated biphenyls from the atmosphere [J].
Anderson, PN ;
Hites, RA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1996, 30 (05) :1756-1763
[2]   Testing the daytime oxidizing capacity of the troposphere: 1994 OH field campaign at the Izana Observatory, Tenerife [J].
Armerding, W ;
Comes, FJ ;
Crawack, HJ ;
Forberich, O ;
Gold, G ;
Ruger, C ;
Spiekermann, M ;
Walter, J ;
Cuevas, E ;
Redondas, A ;
Schmitt, R ;
Matuska, P .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1997, 102 (D9) :10603-10611
[3]   RATE CONSTANTS FOR THE GAS-PHASE REACTION OF HYDROXYL RADICALS WITH BIPHENYL AND THE MONOCHLOROBIPHENYLS AT 295+/-1-K [J].
ATKINSON, R ;
ASCHMANN, SM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1985, 19 (05) :462-464
[4]   KINETICS AND PRODUCTS OF THE GAS-PHASE REACTIONS OF OH RADICALS AND N2O5 WITH NAPHTHALENE AND BIPHENYL [J].
ATKINSON, R ;
AREY, J ;
ZIELINSKA, B ;
ASCHMANN, SM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1987, 21 (10) :1014-1022
[5]   GAS-PHASE TROPOSPHERIC CHEMISTRY OF ORGANIC-COMPOUNDS - A REVIEW [J].
ATKINSON, R .
ATMOSPHERIC ENVIRONMENT PART A-GENERAL TOPICS, 1990, 24 (01) :1-41
[6]   ATMOSPHERIC LIFETIMES OF DIBENZO-PARA-DIOXINS AND DIBENZOFURANS [J].
ATKINSON, R .
SCIENCE OF THE TOTAL ENVIRONMENT, 1991, 104 (1-2) :17-33
[7]  
ATKINSON R, 1985, CHEM REV, V85, P69
[8]  
Atkinson R., 1989, J. Phys. Chem. Ref. Data, V1, P1
[9]   Diffusive exchange of polycyclic aromatic hydrocarbons across the air-water interface of the Patapsco River, an urbanized subestuary of the Chesapeake Bay [J].
Bamford, HA ;
Offenberg, JH ;
Larsen, RK ;
Ko, FC ;
Baker, JE .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1999, 33 (13) :2138-2144
[10]   Gas phase oxidation products of biphenyl and polychlorinated biphenyls [J].
Brubaker, WW ;
Hites, RA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (24) :3913-3918