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Americium binding to humic acid.

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Americium binding to humic acid. / Peters, Adam J.; Hamilton-Taylor, John; Tipping, Edward.
In: Environmental Science and Technology, Vol. 35, No. 17, 01.09.2001, p. 3495-3500.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Peters, AJ, Hamilton-Taylor, J & Tipping, E 2001, 'Americium binding to humic acid.', Environmental Science and Technology, vol. 35, no. 17, pp. 3495-3500. https://doi.org/10.1021/es000295g

APA

Peters, A. J., Hamilton-Taylor, J., & Tipping, E. (2001). Americium binding to humic acid. Environmental Science and Technology, 35(17), 3495-3500. https://doi.org/10.1021/es000295g

Vancouver

Peters AJ, Hamilton-Taylor J, Tipping E. Americium binding to humic acid. Environmental Science and Technology. 2001 Sept 1;35(17):3495-3500. doi: 10.1021/es000295g

Author

Peters, Adam J. ; Hamilton-Taylor, John ; Tipping, Edward. / Americium binding to humic acid. In: Environmental Science and Technology. 2001 ; Vol. 35, No. 17. pp. 3495-3500.

Bibtex

@article{ecbeb053823347f281c0ba12caf2e71e,
title = "Americium binding to humic acid.",
abstract = "The binding of americium (Am) by peat humic acid (PHA) has been investigated at Am concentrations between 10-11 and 10-7 M at pH 2.6 in the presence and absence of Cu as a competing ion. Cu−PHA binding was also investigated in order to derive independent binding constants for use in modeling the competitive binding studies. Humic ion-binding model VI was used to compare the acquired data with previously published binding data and to investigate the importance of high-affinity binding sites in metal−PHA binding. Am was not observed to bind to high-affinity, low-concentration binding sites. The model VI parameter ΔLK2 takes into account the small number of strong sites in PHA and was found to be important for Cu−PHA binding but not for Am−PHA binding, regardless of whether Cu was present. Analysis of the PHA sample revealed that it contained a considerable quantity of Fe not removed by the extraction procedure, much of which is believed to be present as Fe(III). Model VI was then used to investigate the possible importance of the presence of Fe(III) in the Am−PHA binding experiments. When Fe(III) was assumed to be present, improved descriptions of the data by model VI were obtained by assuming that all of the metals [Am, Cu, and Fe(III)] undergo strong binding. This highlights the importance of Fe(III) competition in metal−PHA binding studies and possible shortcomings in the extraction procedure used to extract PHA.",
author = "Peters, {Adam J.} and John Hamilton-Taylor and Edward Tipping",
year = "2001",
month = sep,
day = "1",
doi = "10.1021/es000295g",
language = "English",
volume = "35",
pages = "3495--3500",
journal = "Environmental Science and Technology",
issn = "0013-936X",
publisher = "American Chemical Society",
number = "17",

}

RIS

TY - JOUR

T1 - Americium binding to humic acid.

AU - Peters, Adam J.

AU - Hamilton-Taylor, John

AU - Tipping, Edward

PY - 2001/9/1

Y1 - 2001/9/1

N2 - The binding of americium (Am) by peat humic acid (PHA) has been investigated at Am concentrations between 10-11 and 10-7 M at pH 2.6 in the presence and absence of Cu as a competing ion. Cu−PHA binding was also investigated in order to derive independent binding constants for use in modeling the competitive binding studies. Humic ion-binding model VI was used to compare the acquired data with previously published binding data and to investigate the importance of high-affinity binding sites in metal−PHA binding. Am was not observed to bind to high-affinity, low-concentration binding sites. The model VI parameter ΔLK2 takes into account the small number of strong sites in PHA and was found to be important for Cu−PHA binding but not for Am−PHA binding, regardless of whether Cu was present. Analysis of the PHA sample revealed that it contained a considerable quantity of Fe not removed by the extraction procedure, much of which is believed to be present as Fe(III). Model VI was then used to investigate the possible importance of the presence of Fe(III) in the Am−PHA binding experiments. When Fe(III) was assumed to be present, improved descriptions of the data by model VI were obtained by assuming that all of the metals [Am, Cu, and Fe(III)] undergo strong binding. This highlights the importance of Fe(III) competition in metal−PHA binding studies and possible shortcomings in the extraction procedure used to extract PHA.

AB - The binding of americium (Am) by peat humic acid (PHA) has been investigated at Am concentrations between 10-11 and 10-7 M at pH 2.6 in the presence and absence of Cu as a competing ion. Cu−PHA binding was also investigated in order to derive independent binding constants for use in modeling the competitive binding studies. Humic ion-binding model VI was used to compare the acquired data with previously published binding data and to investigate the importance of high-affinity binding sites in metal−PHA binding. Am was not observed to bind to high-affinity, low-concentration binding sites. The model VI parameter ΔLK2 takes into account the small number of strong sites in PHA and was found to be important for Cu−PHA binding but not for Am−PHA binding, regardless of whether Cu was present. Analysis of the PHA sample revealed that it contained a considerable quantity of Fe not removed by the extraction procedure, much of which is believed to be present as Fe(III). Model VI was then used to investigate the possible importance of the presence of Fe(III) in the Am−PHA binding experiments. When Fe(III) was assumed to be present, improved descriptions of the data by model VI were obtained by assuming that all of the metals [Am, Cu, and Fe(III)] undergo strong binding. This highlights the importance of Fe(III) competition in metal−PHA binding studies and possible shortcomings in the extraction procedure used to extract PHA.

U2 - 10.1021/es000295g

DO - 10.1021/es000295g

M3 - Journal article

VL - 35

SP - 3495

EP - 3500

JO - Environmental Science and Technology

JF - Environmental Science and Technology

SN - 0013-936X

IS - 17

ER -