Reactivity of certain organophosphorus insecticides toward hydroxyl radicals at elevated air temperatures

被引:20
作者
Hebert, VR [1 ]
Hoonhout, C [1 ]
Miller, GC [1 ]
机构
[1] Univ Nevada, Dept Environm & Resource Sci, Reno, NV 89557 USA
关键词
gas phase; hydroxyl radical; organophosphorus insecticide; SPME;
D O I
10.1021/jf9907283
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Methods were developed to determine OH reaction rates for medium-weight organophosphorus pesticides in the gas phase. A 57-L chamber was constructed that utilized xenon are irradiation ( >290 nm) to photolyze the OH precursor, methyl nitrite. Experiments were performed at elevated temperatures ranging from 60 to 80 degrees C to minimize wall sorption. Solid-phase microextraction (SPME) sampling of the gas phase was employed to assess the simultaneous rate of loss of the pesticides in relation to the rate of loss of two reference substances with known OH rate constants. An internal gas-phase standard (hexachlorobenzene), relatively stable to hydroxyl radicals, was used to assess other processes, which included dilution and wall sorption. The relative reaction rates of the organophosphorus insecticides, diazinon and chlorpyrifos, when compared to reference compounds, were unaffected by various air temperatures between 60 and 80 degrees C. Although both insecticides were expected to react at similar rates on the basis of structural activity model predictions, diazinon reacted 3 times more rapidly than chlorpyrifos and gave estimated environmental OH half-lives of 0.5 and 1.4 h, respectively. The degree of sorption onto the chamber walls was minimal and similar for each of the compounds examined. Experimental gas-phase determinations at elevated temperatures may protide important information that can be used when in the assessment of the potential of airborne pesticide risks to nontarget and ecologically sensitive areas.
引用
收藏
页码:1922 / 1928
页数:7
相关论文
共 25 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
[3]   PRODUCT FORMATION FROM THE GAS-PHASE REACTIONS OF THE OH RADICAL WITH (CH3O)3PS AND (CH3O)2P(S)SCH3 [J].
ATKINSON, R ;
ASCHMANN, SM ;
AREY, J ;
MCELROY, PA ;
WINER, AM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1989, 23 (02) :243-244
[4]   REMOTE SCANNING ULTRAVIOLET DETECTION FOR CAPILLARY GAS-CHROMATOGRAPHY [J].
BORNHOP, DJ ;
HLOUSEK, L ;
HACKETT, M ;
WANG, H ;
MILLER, GC .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1992, 63 (01) :191-201
[5]   OH reaction kinetics of gas-phase α- and γ-hexachlorocyclohexane and hexachlorobenzene [J].
Brubaker, WW ;
Hites, RA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (06) :766-769
[6]   ATMOSPHERIC REACTIONS OF A SERIES OF DIMETHYL PHOSPHOROAMIDATES AND DIMETHYL PHOSPHOROTHIOAMIDATES [J].
GOODMAN, MA ;
ASCHMANN, SM ;
ATKINSON, R ;
WINER, AM .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1988, 22 (05) :578-583
[7]   ULTRAVIOLET-VISIBLE DETECTION FOR CAPILLARY GAS-CHROMATOGRAPHY AND COMBINED ULTRAVIOLET MASS-SPECTROMETRY USING A REMOTE FLOW CELL [J].
HACKETT, M ;
WANG, HL ;
MILLER, GC ;
BORNHOP, DJ .
JOURNAL OF CHROMATOGRAPHY A, 1995, 695 (02) :243-257
[8]   Use of stable tracer studies to evaluate pesticide photolysis at elevated temperatures [J].
Hebert, VR ;
Hoonhout, C ;
Miller, GC .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2000, 48 (05) :1916-1921
[9]  
KIM Y, 1985, THESIS U CALIF, P1
[10]   RATE CONSTANTS FOR THE GAS-PHASE REACTIONS OF THE OH RADICAL WITH DICHLOROBIPHENYLS, 1-CHLORODIBENZO-P-DIOXIN, 1,2-DIMETHOXYBENZENE, AND DIPHENYL ETHER - ESTIMATION OF OH RADICAL REACTION-RATE CONSTANTS FOR PCBS, PCDDS, AND PCDFS [J].
KWOK, ESC ;
ATKINSON, R ;
AREY, J .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1995, 29 (06) :1591-1598