Uptake and UV-photooxidation of gas-phase PAHs on the surface of atmospheric water films. 1. Naphthalene

被引:42
作者
Chen, Jing [1 ]
Ehrenhauser, Franz S. [1 ]
Valsaraj, Kalliat T. [1 ]
Wornat, Mary J. [1 ]
机构
[1] Louisiana State Univ, Cain Dept Chem Engn, Baton Rouge, LA 70803 USA
关键词
POLYNUCLEAR AROMATIC-HYDROCARBONS; FOG DROPLETS; OXIDATION; ADSORPTION; INTERFACE; OZONE; IRRADIATION; MECHANISMS; CHEMISTRY; RADIATION;
D O I
10.1021/jp062560b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The adsorption and photochemical reaction of naphthalene vapor at the air-water interface of water films ( 22 Am and 450 Am) were studied in a horizontal flow reactor. Experiments were conducted in the regime where gas-phase mass transfer resistance did not limit the uptake. The equilibrium uptake was dependent on water film thickness only below 1 Am. Bulk water-air and air-to-interface partition constants were estimated from the experiments. The equilibrium partition constant between the water film and air decreased with increasing temperature. Photochemical reaction products were isolated in the water film after exposure to UV light. Four main oxygenated products were identified (1,3- indandione, 1(3H)-isobenzofuranone ( phthalide), 2H-1-benzopyran-2-one (coumarin), and 1-naphthol). The initial rates of product formation were 46 to 154% larger for the thin film (22 mu m) compared to both a thick film ( 450 Am) and bulk aqueous phase photooxidation. The atmospheric implications of reactions in water films are discussed.
引用
收藏
页码:9161 / 9168
页数:8
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