4.8 Article

In Situ Photocatalytic Synthesis of Ag Nanoparticles (nAg) by Crumpled Graphene Oxide Composite Membranes for Filtration and Disinfection Applications

Journal

ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 50, Issue 5, Pages 2514-2521

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.5b04584

Keywords

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Funding

  1. National Science Foundation's CAREER Award [CBET 1454656]
  2. McDonnell Academy Global Energy and Environment Partnership (MAGEEP), Washington University in St. Louis
  3. National Science Foundation [ECS-0335765]
  4. Div Of Chem, Bioeng, Env, & Transp Sys
  5. Directorate For Engineering [1454656] Funding Source: National Science Foundation

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Graphene oxide (GO) materials have demonstrated considerable potential in next-generation water treatment membrane-based technologies, which include antimicrobial applications. GO antimicrobial properties can be further enhanced by preloading or chemically generating surface associated nanoscale silver particles (nAg). However, for these systems, enhanced antimicrobial functionality decreases over time as a function of Ag mass loss via dissolution (as Ag+). In this work, we demonstrate facile photocatalytic in situ synthesis of nAg particles by crumpled GO-TiO2 (GOTI) nanocomposites as an approach to (re)generate, and thus maintain, enhanced antimicrobial activity over extended operation times. The described photocatalytic formation process is highly efficient and relatively fast, producing nAg particles over a size range of 40 to 120 nm and with active (111) planes. Additionally, we show in situ surface-based photocatalyzed synthesis of nAg particles at the surface of GOTI nanocomposite membrane assemblies, allowing for simultaneous filtration and disinfection. With ca. 3 log inactivation for both Escherichia coli and Bacillus subtilis, the described membrane assemblies with in situ formed nAg demonstrate enhanced antimicrobial activity compared to the GOTI membrane surface or the support membrane alone. Under typical conditions, the working and operational time (Ag dissolution time) is calculated to be over 2 orders of magnitude higher than the loading (synthesis) time (e.g., 123 h versus 0.5 h, respectively). Taken together, results highlight the described material based process as a potentially novel antifouling membrane technology.

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