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Transport and sorption behavior of individual phthalate esters in sandy aquifer: column experiments. | LitMetric

Transport and sorption behavior of individual phthalate esters in sandy aquifer: column experiments.

Environ Sci Pollut Res Int

State Key Laboratory of Biogeology and Environmental Geology and School of Environmental Studies, China University of Geosciences, Wuhan, 430074, People's Republic of China.

Published: August 2016

AI Article Synopsis

  • This study investigates how four different phthalate esters (PAEs) behave in sandy aquifers using column experiments to understand their transport and sorption dynamics for better groundwater pollution management.
  • The researchers used HYDRUS-1D software to model transport curves, finding that two-site sorption models (LFO and NFO) provided the best fits, revealing unexpected transport patterns of PAEs based on their carbon chain lengths.
  • The results showed shorter carbon chain PAEs (DMP and DEP) migrated less distance compared to longer chain PAEs (DBP and DiBP) due to differences in how these compounds interact with available sorption sites in the soil.

Article Abstract

This work aimed to quantify the transport and sorption behavior of four individual phthalate esters (PAEs) in sandy aquifer using column experiments so as to provide important parameters for the prediction and control of PAEs pollution plume in groundwater system. The transport curves of four individual PAEs were simulated with HYDRUS-1D through fitting linear and nonlinear equilibrium (LE/NO), linear and nonlinear, first-order, one-site non-equilibrium (LO/NO), linear and nonlinear, first-order, two-site non-equilibrium (LFO/NFO) sorption models. Simulation results showed that two-site models (LFO and NFO) displayed similar best fittings. The results from LFO model simulation showed that when water flowed 1000 m in sandy aquifer, PAEs with shorter carbon chains (DMP and DEP) transport 31.6 and 22.2 m, respectively. Unexpectedly for the same water transport distance, PAEs with longer carbon chains (DBP and DiBP) transported 40.2 and 60.7 m, respectively, which were faster than DMP and DEP, mainly due to the limited accessibility of type-2 sorption sites. The retardations were mainly caused by the sorption of PAEs on the time-dependent type-2 sites. DBP and DiBP exhibited higher mass transfer speed to and fro type-2 sites but showed lower total sorption coefficient (K) due to the limited accessibility of sorption sites. Coexistence of PAEs and smaller sorbent particles increased total K values of DBP and DiBP due to synergic development of more sorption sites with DMP and DEP.

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Source
http://dx.doi.org/10.1007/s11356-016-6660-yDOI Listing

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