Abstract

Only a limited and scattered knowledge is currently available on the conditions leading to the occurrence of sampling alteration at low ionic strength (<10−3 mol L−1) with DGT (diffusive gradients in thin films technique). In this study, the role of the pH and the charge of the analyte were comprehensively evaluated with DGT equipped with APA (polyacrylamide with agarose-derivative crosslinker) diffusive gels and ZrO or Chelex binding phases. The sampling of four cations (CdII, CuII, NiII and PbII) and two anions (AsV and CrVI) was compared for pH 4, 6 and 8 at common (10−2 mol L−1) and low (10−4 mol L−1) ionic strengths. Results showed that the sampling was modified at low ionic strength only in the most acidic condition (pH 4) for both anions and cations with an opposite incidence: cations' sampling was halved whereas anions’ sampling was increased. Furthermore, cations sampling alteration was similarly reproduced using diffusion cell experiments, which requires only the APA gel, indicating that the binding layer does not participate in the low ionic strength effect. The intensity of DGT sampling modification was consistent with a prediction based on Donnan partitioning of analytes at gel/solution interface for several valences (from -I to + III). All these results strongly suggest that the APA diffusive gels carry positive charges that create a Donnan effect at low ionic strength. Since no ionic strength effect could be evidenced at pH 6 and 8, it can be reasonably assumed that this effect occurs only marginally for DGT deployments in most natural waters.

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