Attachment of silver nanoparticles (AgNPs) onto thin-film composite (TFC) membranes through covalent bonding to reduce membrane biofouling

Membrane biofouling has a negative impact on the membrane treatment performance. Silver nanoparticles (AgNPs) are well-known antimicrobial agent. Herein, AgNPs with approximately 15nm in diameter were effectively attached to the surface of polyamide (PA) thin-film composite (TFC) membrane via covale...

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Published inJournal of membrane science Vol. 441; pp. 73 - 82
Main Authors Yin, Jun, Yang, Yu, Hu, Zhiqiang, Deng, Baolin
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.08.2013
Elsevier
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Abstract Membrane biofouling has a negative impact on the membrane treatment performance. Silver nanoparticles (AgNPs) are well-known antimicrobial agent. Herein, AgNPs with approximately 15nm in diameter were effectively attached to the surface of polyamide (PA) thin-film composite (TFC) membrane via covalent bonding, with cysteamine as a bridging agent. Scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and cross-sectional transmission electron microscopy (TEM) studies all showed the immobilization of AgNPs. Compared with the pristine TFC membrane, thiol-terminated membrane (TFC–SH) and AgNPs grafted membrane (TFC-S–AgNPs) both showed a higher water flux with slightly lower salt rejection. At a constant transmenbrane pressure of 300psi, the water permeability of TFC–SH, TFC-S–AgNPs, and control TFC membranes was 70.6±0.5, 69.4±0.3, and 49.8±1.7L/m2h, respectively, while NaCl rejection was 93.4±0.1%, 93.6±0.2%, and 95.9±0.6%, respectively. TFC-S–AgNPs had an improved antibacterial ability to inhibit E. coli growth. The silver leaching from the TFC-S–AgNPs membrane surfaces was minimal, as tested by both batch and flow-through methods. The results successfully demonstrated that AgNPs could be grafted onto TFC via chemical bonding, leading towards the development of an advanced functional TFC membrane with anti-biofouling properties. •AgNPs around 15nm in diameter were synthesized via chemical reduction.•AgNPs were effectively attached to the membrane surface via covalent bonding.•Effects of grafting conditions on membrane performance.•Silver ions releases were assessed via both batch and flow-through experiments.•Biofilm growth test was carried out on a drip flow biofilm reactor.
AbstractList Membrane biofouling has a negative impact on the membrane treatment performance. Silver nanoparticles (AgNPs) are well-known antimicrobial agent. Herein, AgNPs with approximately 15 nm in diameter were effectively attached to the surface of polyamide (PA) thin-film composite (TFC) membrane via covalent bonding, with cysteamine as a bridging agent. Scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and cross-sectional transmission electron microscopy (TEM) studies all showed the immobilization of AgNPs. Compared with the pristine TFC membrane, thiol-terminated membrane (TFCaSH) and AgNPs grafted membrane (TFC-SaAgNPs) both showed a higher water flux with slightly lower salt rejection. At a constant transmenbrane pressure of 300 psi, the water permeability of TFCaSH, TFC-SaAgNPs, and control TFC membranes was 70.6A-0.5, 69.4A-0.3, and 49.8A-1.7 L/m2h, respectively, while NaCl rejection was 93.4A-0.1%, 93.6A-0.2%, and 95.9A-0.6%, respectively. TFC-SaAgNPs had an improved antibacterial ability to inhibit E. coli growth. The silver leaching from the TFC-SaAgNPs membrane surfaces was minimal, as tested by both batch and flow-through methods. The results successfully demonstrated that AgNPs could be grafted onto TFC via chemical bonding, leading towards the development of an advanced functional TFC membrane with anti-biofouling properties.
Membrane biofouling has a negative impact on the membrane treatment performance. Silver nanoparticles (AgNPs) are well-known antimicrobial agent. Herein, AgNPs with approximately 15nm in diameter were effectively attached to the surface of polyamide (PA) thin-film composite (TFC) membrane via covalent bonding, with cysteamine as a bridging agent. Scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and cross-sectional transmission electron microscopy (TEM) studies all showed the immobilization of AgNPs. Compared with the pristine TFC membrane, thiol-terminated membrane (TFC–SH) and AgNPs grafted membrane (TFC-S–AgNPs) both showed a higher water flux with slightly lower salt rejection. At a constant transmenbrane pressure of 300psi, the water permeability of TFC–SH, TFC-S–AgNPs, and control TFC membranes was 70.6±0.5, 69.4±0.3, and 49.8±1.7L/m²h, respectively, while NaCl rejection was 93.4±0.1%, 93.6±0.2%, and 95.9±0.6%, respectively. TFC-S–AgNPs had an improved antibacterial ability to inhibit E. coli growth. The silver leaching from the TFC-S–AgNPs membrane surfaces was minimal, as tested by both batch and flow-through methods. The results successfully demonstrated that AgNPs could be grafted onto TFC via chemical bonding, leading towards the development of an advanced functional TFC membrane with anti-biofouling properties.
Membrane biofouling has a negative impact on the membrane treatment performance. Silver nanoparticles (AgNPs) are well-known antimicrobial agent. Herein, AgNPs with approximately 15nm in diameter were effectively attached to the surface of polyamide (PA) thin-film composite (TFC) membrane via covalent bonding, with cysteamine as a bridging agent. Scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and cross-sectional transmission electron microscopy (TEM) studies all showed the immobilization of AgNPs. Compared with the pristine TFC membrane, thiol-terminated membrane (TFC–SH) and AgNPs grafted membrane (TFC-S–AgNPs) both showed a higher water flux with slightly lower salt rejection. At a constant transmenbrane pressure of 300psi, the water permeability of TFC–SH, TFC-S–AgNPs, and control TFC membranes was 70.6±0.5, 69.4±0.3, and 49.8±1.7L/m2h, respectively, while NaCl rejection was 93.4±0.1%, 93.6±0.2%, and 95.9±0.6%, respectively. TFC-S–AgNPs had an improved antibacterial ability to inhibit E. coli growth. The silver leaching from the TFC-S–AgNPs membrane surfaces was minimal, as tested by both batch and flow-through methods. The results successfully demonstrated that AgNPs could be grafted onto TFC via chemical bonding, leading towards the development of an advanced functional TFC membrane with anti-biofouling properties. •AgNPs around 15nm in diameter were synthesized via chemical reduction.•AgNPs were effectively attached to the membrane surface via covalent bonding.•Effects of grafting conditions on membrane performance.•Silver ions releases were assessed via both batch and flow-through experiments.•Biofilm growth test was carried out on a drip flow biofilm reactor.
Author Deng, Baolin
Hu, Zhiqiang
Yang, Yu
Yin, Jun
Author_xml – sequence: 1
  givenname: Jun
  surname: Yin
  fullname: Yin, Jun
  organization: Department of Civil & Environmental Engineering, University of Missouri, Columbia, MO 65211, USA
– sequence: 2
  givenname: Yu
  surname: Yang
  fullname: Yang, Yu
  organization: Department of Civil & Environmental Engineering, University of Missouri, Columbia, MO 65211, USA
– sequence: 3
  givenname: Zhiqiang
  surname: Hu
  fullname: Hu, Zhiqiang
  organization: Department of Civil & Environmental Engineering, University of Missouri, Columbia, MO 65211, USA
– sequence: 4
  givenname: Baolin
  surname: Deng
  fullname: Deng, Baolin
  email: dengb@missouri.edu
  organization: Department of Civil & Environmental Engineering, University of Missouri, Columbia, MO 65211, USA
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Keywords Thiol group
Polyamide
Covalent bonding
Anti-biofouling
Thin-film composite
Silver nanoparticles
Thiol
Nylon
Nanoparticle
Transition metal
Antimicrobial agent
Composite material
Thin film
Silver
Biofouling
Membrane
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Snippet Membrane biofouling has a negative impact on the membrane treatment performance. Silver nanoparticles (AgNPs) are well-known antimicrobial agent. Herein, AgNPs...
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SubjectTerms Anti-biofouling
anti-infective agents
Antiinfectives and antibacterials
Applied sciences
artificial membranes
Biofouling
Bonding
chemical bonding
Composites
Covalent bonding
cysteamine
energy
energy-dispersive X-ray analysis
Escherichia coli
Exact sciences and technology
Forms of application and semi-finished materials
Grafting
leaching
Membranes
nanosilver
permeability
Polyamide
polyamides
Polymer industry, paints, wood
Rejection
Scanning electron microscopy
Silver
Silver nanoparticles
sodium chloride
spectroscopy
Technology of polymers
Thin films
Thin-film composite
Thiol group
transmission electron microscopy
X-radiation
Title Attachment of silver nanoparticles (AgNPs) onto thin-film composite (TFC) membranes through covalent bonding to reduce membrane biofouling
URI https://dx.doi.org/10.1016/j.memsci.2013.03.060
https://www.proquest.com/docview/1513464685
https://www.proquest.com/docview/1753553005
https://www.proquest.com/docview/1803130508
Volume 441
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