Modeling Uptake of Hydrophobic Organic Contaminants into Polyethylene Passive Samplers

被引:40
|
作者
Thompson, Jay M. [1 ]
Hsieh, Ching-Hong [1 ]
Luthy, Richard G. [1 ]
机构
[1] Stanford Univ, Dept Civil & Environm Engn, Stanford, CA 94305 USA
关键词
LOW-DENSITY POLYETHYLENE; FREELY DISSOLVED CONCENTRATIONS; DIFFUSION-COEFFICIENTS; PORE-WATER; ORGANOCHLORINE PESTICIDES; SEDIMENT; PAHS; POLYMERS; DEVICES; PCBS;
D O I
10.1021/es504442s
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Single-phase passive samplers are gaining acceptance as a method to measure hydrophobic organic contaminant (HOC) concentration in water. Although the relationship between the HOC concentration in water and passive sampler is linear at equilibrium, mass transfer models are needed for nonequilibrium conditions. We report measurements of organochlorine pesticide diffusion and partition coefficients with respect to polyethylene (PE), and present a Fickian approach to modeling HOC uptake by PE in aqueous systems. The model is an analytic solution to Ficks second law applied through an aqueous diffusive boundary layer and a polyethylene layer. Comparisons of the model with existing methods indicate agreement at appropriate boundary conditions. Laboratory release experiments on the organochlorine pesticides DDT, DDE, DDD, and chlordane in well-mixed slurries support the models applicability to aqueous systems. In general, the advantage of the model is its application in the cases of well-agitated systems, low values of polyethylenewater partioning coefficients, thick polyethylene relative to the boundary layer thickness, and/or short exposure times. Another significant advantage is the ability to estimate, or at least bound, the needed exposure time to reach a desired C-PE without empirical model inputs. A further finding of this work is that polyethylene diffusivity does not vary by transport direction through the sampler thickness.
引用
收藏
页码:2270 / 2277
页数:8
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