Effect of pH on the adsorption of carbendazim in Polish mineral soils

被引:19
|
作者
Paszko, Tadeusz [1 ]
机构
[1] Univ Life Sci, Dept Chem, PL-20950 Lublin, Poland
关键词
Carbendazim; Soil horizons; Adsorption; pH; Modeling; IONIZABLE PESTICIDES; SORPTION-DESORPTION; CATION-EXCHANGE; ORGANIC-BASES; MONTMORILLONITE; WATER; ATRAZINE; BIOAVAILABILITY; TRANSFORMATION; DEGRADATION;
D O I
10.1016/j.scitotenv.2012.07.013
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The study aimed to determine the influence of pH on the adsorption of carbendazim in soil profiles of three mineral agricultural soils: Hyperdystric Arenosol, Haplic Luvisol and Hypereutric Cambisol. In the examined pH range between 3 and 7 the adsorption of carbendazim was inversely correlated to the pH of the soil. The adsorption coefficients were in the range between 0.3 and 151.8 mL g(-1). Decreasing the pH in the soil suspensions from 7 to 3 increased the value of this coefficient by 3 to 70 times. A decrease in the amounts of organic matter down the soil profiles was not associated with weaker carbendazim adsorption. In the samples from all soil horizons, at pH values between 3 and 6, the predominant sorption process was carbendazim adsorption on clay minerals. The adsorption of carbendazim on organic matter prevailed over that on clays only at pH > 6 and only in the Ap horizon of the examined soils. The developed mathematical models yielded very good results when the adsorption of the protonated form of carbendazim was assumed to be the predominant adsorption process on clays together with the adsorption of neutral molecules on organic matter and clays. The results from both the model fitting and the experiments revealed the negative effect of Al oxides and hydroxides and Al cations on the adsorption of the protonated form of carbendazim on clay minerals. The developed models successfully described the pH-dependent adsorption processes of carbendazim for both data from particular soil horizons and those from all three examined soil profiles. (c) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:222 / 229
页数:8
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