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Measurement of metals Using DGT: impact of ionic strength and kinetics of dissociation of complexes in the resin domain

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Measurement of metals Using DGT: impact of ionic strength and kinetics of dissociation of complexes in the resin domain. / Puy, Jaume; Galceran, Josep; Cruz-González, Sara et al.
In: Analytical Chemistry, Vol. 86, No. 15, 05.08.2014, p. 7740-7748.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Puy, J, Galceran, J, Cruz-González, S, David, CA, Uribe, R, Lin, C, Zhang, H & Davison, W 2014, 'Measurement of metals Using DGT: impact of ionic strength and kinetics of dissociation of complexes in the resin domain', Analytical Chemistry, vol. 86, no. 15, pp. 7740-7748. https://doi.org/10.1021/ac501679m

APA

Puy, J., Galceran, J., Cruz-González, S., David, C. A., Uribe, R., Lin, C., Zhang, H., & Davison, W. (2014). Measurement of metals Using DGT: impact of ionic strength and kinetics of dissociation of complexes in the resin domain. Analytical Chemistry, 86(15), 7740-7748. https://doi.org/10.1021/ac501679m

Vancouver

Puy J, Galceran J, Cruz-González S, David CA, Uribe R, Lin C et al. Measurement of metals Using DGT: impact of ionic strength and kinetics of dissociation of complexes in the resin domain. Analytical Chemistry. 2014 Aug 5;86(15):7740-7748. Epub 2014 Jul 11. doi: 10.1021/ac501679m

Author

Puy, Jaume ; Galceran, Josep ; Cruz-González, Sara et al. / Measurement of metals Using DGT : impact of ionic strength and kinetics of dissociation of complexes in the resin domain. In: Analytical Chemistry. 2014 ; Vol. 86, No. 15. pp. 7740-7748.

Bibtex

@article{abc1f3b29dc84239b6e9623177a032d8,
title = "Measurement of metals Using DGT: impact of ionic strength and kinetics of dissociation of complexes in the resin domain",
abstract = "As the measurement of metals by DGT (diffusion gradients in thin films) in low salinity media has been controversial, a thorough study of the impact of ionic strength (I) is timely. DGT accumulations of Cd, Co, and Ni in the presence of NTA at pH 7.5 with I in the range from 10–4 to 0.5 M were obtained. An observed decrease in the metal accumulation as the ionic strength of the system decreased is partially explained by the electrostatic repulsion between the negatively charged resin domain and the dominant negatively charged complex species M–NTA. This electrostatic effect reduces the complex penetration into the resin domain, especially for nonlabile complexes, which do not fully dissociate in the gel domain. Analytical expressions, based on the Donnan model, were able to quantify these electrostatic effects. Additionally, the data indicate that the kinetic dissociation constant of M–NTA complexes in the resin layer is higher than Eigen predictions, suggesting a ligand-assisted dissociation mechanism. As the ionic strength decreases, the rate of reaction in the resin layer decreases due to the repulsion between the negatively charged resin sites and the complex species. This decrease contributes to the decrease in metal accumulation. These novel, previously unconsidered, effects of ionic strength and the ligand-assisted dissociation mechanism in the resin domain will affect DGT measurements made in freshwaters and soils.",
author = "Jaume Puy and Josep Galceran and Sara Cruz-Gonz{\'a}lez and David, {Calin A.} and Ramiro Uribe and Chun Lin and Hao Zhang and William Davison",
year = "2014",
month = aug,
day = "5",
doi = "10.1021/ac501679m",
language = "English",
volume = "86",
pages = "7740--7748",
journal = "Analytical Chemistry",
issn = "0003-2700",
publisher = "American Chemical Society",
number = "15",

}

RIS

TY - JOUR

T1 - Measurement of metals Using DGT

T2 - impact of ionic strength and kinetics of dissociation of complexes in the resin domain

AU - Puy, Jaume

AU - Galceran, Josep

AU - Cruz-González, Sara

AU - David, Calin A.

AU - Uribe, Ramiro

AU - Lin, Chun

AU - Zhang, Hao

AU - Davison, William

PY - 2014/8/5

Y1 - 2014/8/5

N2 - As the measurement of metals by DGT (diffusion gradients in thin films) in low salinity media has been controversial, a thorough study of the impact of ionic strength (I) is timely. DGT accumulations of Cd, Co, and Ni in the presence of NTA at pH 7.5 with I in the range from 10–4 to 0.5 M were obtained. An observed decrease in the metal accumulation as the ionic strength of the system decreased is partially explained by the electrostatic repulsion between the negatively charged resin domain and the dominant negatively charged complex species M–NTA. This electrostatic effect reduces the complex penetration into the resin domain, especially for nonlabile complexes, which do not fully dissociate in the gel domain. Analytical expressions, based on the Donnan model, were able to quantify these electrostatic effects. Additionally, the data indicate that the kinetic dissociation constant of M–NTA complexes in the resin layer is higher than Eigen predictions, suggesting a ligand-assisted dissociation mechanism. As the ionic strength decreases, the rate of reaction in the resin layer decreases due to the repulsion between the negatively charged resin sites and the complex species. This decrease contributes to the decrease in metal accumulation. These novel, previously unconsidered, effects of ionic strength and the ligand-assisted dissociation mechanism in the resin domain will affect DGT measurements made in freshwaters and soils.

AB - As the measurement of metals by DGT (diffusion gradients in thin films) in low salinity media has been controversial, a thorough study of the impact of ionic strength (I) is timely. DGT accumulations of Cd, Co, and Ni in the presence of NTA at pH 7.5 with I in the range from 10–4 to 0.5 M were obtained. An observed decrease in the metal accumulation as the ionic strength of the system decreased is partially explained by the electrostatic repulsion between the negatively charged resin domain and the dominant negatively charged complex species M–NTA. This electrostatic effect reduces the complex penetration into the resin domain, especially for nonlabile complexes, which do not fully dissociate in the gel domain. Analytical expressions, based on the Donnan model, were able to quantify these electrostatic effects. Additionally, the data indicate that the kinetic dissociation constant of M–NTA complexes in the resin layer is higher than Eigen predictions, suggesting a ligand-assisted dissociation mechanism. As the ionic strength decreases, the rate of reaction in the resin layer decreases due to the repulsion between the negatively charged resin sites and the complex species. This decrease contributes to the decrease in metal accumulation. These novel, previously unconsidered, effects of ionic strength and the ligand-assisted dissociation mechanism in the resin domain will affect DGT measurements made in freshwaters and soils.

U2 - 10.1021/ac501679m

DO - 10.1021/ac501679m

M3 - Journal article

VL - 86

SP - 7740

EP - 7748

JO - Analytical Chemistry

JF - Analytical Chemistry

SN - 0003-2700

IS - 15

ER -