Unhindered copper uptake by glutaraldehyde-polyethyleneimine coatings in an artificial seawater model system with adsorbed swollen polysaccharides and competing ligand EDTA

Simarpreet Kaur; Ivan M. Kempson; Johan B. Lindén; Mikael Larsson; Magnus Nydén

doi:10.1080/08927014.2017.1284204

Unhindered copper uptake by glutaraldehyde-polyethyleneimine coatings in an artificial seawater model system with adsorbed swollen polysaccharides and competing ligand EDTA

Simarpreet Kaur, Ivan M. Kempson, Johan B. Lindén, Mikael Larsson^*, Magnus Nydén

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

10 Citations (Scopus)

Abstract

Shortly after a surface is submerged in the sea, a conditioning film is generally formed by adsorption of organic molecules, such as polysaccharides. This could affect transport of molecules and ions between the seawater and the surface. An artificial seawater model system was developed to understand how adsorbed polysaccharides impact copper binding by glutaraldehyde-crosslinked polyethyleneimine coatings. Coating performance was also determined when competed against copper-chelating EDTA. Polysaccharide adsorption and copper binding and distribution were investigated using advanced analytical techniques, including depth-resolved time-of-flight secondary ion mass spectroscopy, grazing incidence X-ray absorption near-edge spectroscopy, quartz crystal microbalance with dissipation monitoring and X-ray photoelectron spectroscopy. In artificial seawater, the polysaccharides adsorbed in a swollen state that copper readily penetrated and the glutaraldehyde-polyethyleneimine coatings outcompeted EDTA for copper binding. Furthermore, the depth distribution of copper species was determined with nanometre precision. The results are highly relevant for copper-binding and copper-releasing materials in seawater.

Original language	English
Pages (from-to)	184-194
Number of pages	11
Journal	Biofouling
Volume	33
Issue number	2
DOIs	https://doi.org/10.1080/08927014.2017.1284204
Publication status	Published - Feb 2017
Externally published	Yes

Bibliographical note

Funding Information:
The project is supported by the Premier?s Research and Industry Fund grant provided by the South Australian Government Department of State Development. The authors acknowledge that work was performed at the South Australian node of the Australian National Fabrication Facility, a company established under the National Collaborative Research Infrastructure Strategy to provide nano- and micro-fabrication facilities for Australia?s researchers. They also acknowledge the assistance of: John Denman, of the Australian Microscopy & Microanalysis Research Facility at the South Australian Regional Facility, University of South Australia; Andreas Karydas, Mateusz Czyzycki, Alessandro Migliori, Werner Jark and Diane Eichert for support on the experimental chamber for X-ray spectrometry of the International Atomic Energy Agency (IAEA), which is operated in partnership at the X-ray fluorescence beamline at Elettra, for which travel funding was provided by the International Synchrotron Access Program (ISAP) managed by the Australian Synchrotron and funded by the Australian Government; and Peter Kappen and Chris Glover for the bulk XAS measurements undertaken on the X-ray absorption spectroscopy beamline at the Australian Synchrotron, Victoria, Australia.

Publisher Copyright:
© 2017 Informa UK Limited, trading as Taylor & Francis Group.

Copyright:
Copyright 2019 Elsevier B.V., All rights reserved.

Keywords

Antifouling
biocidal metals
copper chelation
kinetics
polyethyleneimine
selective binding

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10.1080/08927014.2017.1284204

Cite this

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title = "Unhindered copper uptake by glutaraldehyde-polyethyleneimine coatings in an artificial seawater model system with adsorbed swollen polysaccharides and competing ligand EDTA",

abstract = "Shortly after a surface is submerged in the sea, a conditioning film is generally formed by adsorption of organic molecules, such as polysaccharides. This could affect transport of molecules and ions between the seawater and the surface. An artificial seawater model system was developed to understand how adsorbed polysaccharides impact copper binding by glutaraldehyde-crosslinked polyethyleneimine coatings. Coating performance was also determined when competed against copper-chelating EDTA. Polysaccharide adsorption and copper binding and distribution were investigated using advanced analytical techniques, including depth-resolved time-of-flight secondary ion mass spectroscopy, grazing incidence X-ray absorption near-edge spectroscopy, quartz crystal microbalance with dissipation monitoring and X-ray photoelectron spectroscopy. In artificial seawater, the polysaccharides adsorbed in a swollen state that copper readily penetrated and the glutaraldehyde-polyethyleneimine coatings outcompeted EDTA for copper binding. Furthermore, the depth distribution of copper species was determined with nanometre precision. The results are highly relevant for copper-binding and copper-releasing materials in seawater.",

keywords = "Antifouling, biocidal metals, copper chelation, kinetics, polyethyleneimine, selective binding",

author = "Simarpreet Kaur and Kempson, {Ivan M.} and Lind{\'e}n, {Johan B.} and Mikael Larsson and Magnus Nyd{\'e}n",

note = "Funding Information: The project is supported by the Premier?s Research and Industry Fund grant provided by the South Australian Government Department of State Development. The authors acknowledge that work was performed at the South Australian node of the Australian National Fabrication Facility, a company established under the National Collaborative Research Infrastructure Strategy to provide nano- and micro-fabrication facilities for Australia?s researchers. They also acknowledge the assistance of: John Denman, of the Australian Microscopy & Microanalysis Research Facility at the South Australian Regional Facility, University of South Australia; Andreas Karydas, Mateusz Czyzycki, Alessandro Migliori, Werner Jark and Diane Eichert for support on the experimental chamber for X-ray spectrometry of the International Atomic Energy Agency (IAEA), which is operated in partnership at the X-ray fluorescence beamline at Elettra, for which travel funding was provided by the International Synchrotron Access Program (ISAP) managed by the Australian Synchrotron and funded by the Australian Government; and Peter Kappen and Chris Glover for the bulk XAS measurements undertaken on the X-ray absorption spectroscopy beamline at the Australian Synchrotron, Victoria, Australia. Publisher Copyright: {\textcopyright} 2017 Informa UK Limited, trading as Taylor & Francis Group. Copyright: Copyright 2019 Elsevier B.V., All rights reserved.",

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doi = "10.1080/08927014.2017.1284204",

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AU - Kempson, Ivan M.

AU - Lindén, Johan B.

AU - Larsson, Mikael

AU - Nydén, Magnus

N1 - Funding Information: The project is supported by the Premier?s Research and Industry Fund grant provided by the South Australian Government Department of State Development. The authors acknowledge that work was performed at the South Australian node of the Australian National Fabrication Facility, a company established under the National Collaborative Research Infrastructure Strategy to provide nano- and micro-fabrication facilities for Australia?s researchers. They also acknowledge the assistance of: John Denman, of the Australian Microscopy & Microanalysis Research Facility at the South Australian Regional Facility, University of South Australia; Andreas Karydas, Mateusz Czyzycki, Alessandro Migliori, Werner Jark and Diane Eichert for support on the experimental chamber for X-ray spectrometry of the International Atomic Energy Agency (IAEA), which is operated in partnership at the X-ray fluorescence beamline at Elettra, for which travel funding was provided by the International Synchrotron Access Program (ISAP) managed by the Australian Synchrotron and funded by the Australian Government; and Peter Kappen and Chris Glover for the bulk XAS measurements undertaken on the X-ray absorption spectroscopy beamline at the Australian Synchrotron, Victoria, Australia. Publisher Copyright: © 2017 Informa UK Limited, trading as Taylor & Francis Group. Copyright: Copyright 2019 Elsevier B.V., All rights reserved.

PY - 2017/2

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N2 - Shortly after a surface is submerged in the sea, a conditioning film is generally formed by adsorption of organic molecules, such as polysaccharides. This could affect transport of molecules and ions between the seawater and the surface. An artificial seawater model system was developed to understand how adsorbed polysaccharides impact copper binding by glutaraldehyde-crosslinked polyethyleneimine coatings. Coating performance was also determined when competed against copper-chelating EDTA. Polysaccharide adsorption and copper binding and distribution were investigated using advanced analytical techniques, including depth-resolved time-of-flight secondary ion mass spectroscopy, grazing incidence X-ray absorption near-edge spectroscopy, quartz crystal microbalance with dissipation monitoring and X-ray photoelectron spectroscopy. In artificial seawater, the polysaccharides adsorbed in a swollen state that copper readily penetrated and the glutaraldehyde-polyethyleneimine coatings outcompeted EDTA for copper binding. Furthermore, the depth distribution of copper species was determined with nanometre precision. The results are highly relevant for copper-binding and copper-releasing materials in seawater.

AB - Shortly after a surface is submerged in the sea, a conditioning film is generally formed by adsorption of organic molecules, such as polysaccharides. This could affect transport of molecules and ions between the seawater and the surface. An artificial seawater model system was developed to understand how adsorbed polysaccharides impact copper binding by glutaraldehyde-crosslinked polyethyleneimine coatings. Coating performance was also determined when competed against copper-chelating EDTA. Polysaccharide adsorption and copper binding and distribution were investigated using advanced analytical techniques, including depth-resolved time-of-flight secondary ion mass spectroscopy, grazing incidence X-ray absorption near-edge spectroscopy, quartz crystal microbalance with dissipation monitoring and X-ray photoelectron spectroscopy. In artificial seawater, the polysaccharides adsorbed in a swollen state that copper readily penetrated and the glutaraldehyde-polyethyleneimine coatings outcompeted EDTA for copper binding. Furthermore, the depth distribution of copper species was determined with nanometre precision. The results are highly relevant for copper-binding and copper-releasing materials in seawater.

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KW - biocidal metals

KW - copper chelation

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ER -

Unhindered copper uptake by glutaraldehyde-polyethyleneimine coatings in an artificial seawater model system with adsorbed swollen polysaccharides and competing ligand EDTA

Abstract

Bibliographical note

Keywords

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