On the photolysis of simple anions and neutral molecules as sources of O-/OH, SOx- and Cl in aqueous solution

被引:182
作者
Herrmann, Hartmut [1 ]
机构
[1] Leibniz Inst Tropospharenforsch, D-04318 Leipzig, Germany
关键词
D O I
10.1039/b618565g
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
This contribution examines the aqueous phase photolysis processes of simple anions such as nitrate, nitrite, peroxodisulfate and neutral molecules such as H2O2. The review includes new results on absolute effective quantum yields for the photodissociation processes of NO3-, NO2-, S2O82-, HSO5-, S2O62-, HOCl, and chloroacetone in an aqueous solution. The quantum yields for the photolysis of nitrate and nitrite have also been determined as a function of temperature. Models to interpret the wavelength and the temperature dependencies of the quantum yields for the different systems are discussed and a simple model treatment is developed to quantify the effects of (i) impulse conservation, (ii) electrostatic interaction (e.g., ion-dipole, dipole-dipole and coulomb interaction between the photofragments directly after photolytic fragmentation), and (iii) diffusion and recombination. The combined impulse-interaction-diffusion (IID) model is compared to the experimentally observed effective radical formation quantum yields and reasonable agreement is found for a number of systems. It is shown that the temperature dependencies for effective quantum yields of photolysis processes in aqueous solution are not only governed by the temperature dependence of the viscosity of water but also determined by the temperature dependence of the rate constants of the photofragment recombination reactions.
引用
收藏
页码:3935 / 3964
页数:30
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