Evaluation of reactivity of pesticides with ozone in water using the energies of frontier molecular orbitals

被引:68
作者
Hu, JY
Morita, T
Magara, Y
Aizawa, T
机构
[1] Natl Inst Publ Hlth, Dept Water Supply Engn, Minato Ku, Tokyo 108, Japan
[2] Hokkaido Univ, Fac Engn, Dept Urban Environm Engn, Kita Ku, Sapporo, Hokkaido 060, Japan
关键词
drinking water treatment; frontier molecular orbital theory; highest occupied molecular orbital; ozone; pesticides; QSAR; rate constants;
D O I
10.1016/S0043-1354(99)00385-1
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The rate constants of ozone with four groups of pesticides (4 phenolic-, 8 organonitrogen-, 8 phenoxyalkylacitic-, and 4 heterocyclic N-pesticides) were determined under controlled conditions at a pH of 7.5, ionic strength of ca 10(-3) M, and 100 mu M NaHCO3. The rate constant for BPMC was first determined from a pseudo-first order reaction model. the rate constants for the other pesticides were then obtained by a competition kinetic method using BPMC as the first reference compound. The rate constants were found to vary widely according to the pesticides. The highest rate constant was 27,600 M-1 s(-1) for PCP and the lowest was 61.8 M-1 s(-1) for cyanazine. In order to quantify the effects of structure on the reactivity of pesticide with ozone, for each group of pesticides the rate constants were correlated with the energies of the highest occupied molecular orbital (epsilon(HOMO)) The logarithm of the rate constants was found to linearly increase with the increase of the epsilon(HOMO) values except for the phenoxyalkylacitic group. When all examined pesticides were included in the correlation analysis. the rate constants gave a statistically unsatisfactory correlation with a coefficient of 0.92, but showed a similar trend of increasing reactivity with increasing epsilon(HOMO) values of pesticides. The results of the correlation analysis suggested that the reactivity of pesticides with ozone follows the frontier orbital theory and can be estimated by epsilon(HOMO) The rate constants for the phenoxyalkylacitic group could be estimated accurately by a two-parameter QSAR model based on absolute electronegativity and epsilon(HOMO) (C) 2000 Elsevier Science Ltd. Ail rights reserved.
引用
收藏
页码:2215 / 2222
页数:8
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