There is a critical need for new efficient solutions to purify and disinfect water from source to point-of-use, especially for the water contaminated by pathogenic microbes. Traditional disinfection technologies are chemically intensive and limited, either by biofouling or by the irreversible consumption of disinfectants. Herein, we present a scalable methodology to create biocidal and rechargeable nanofibrous membranes (BNF membranes) by combining N-halamine antimicrobial agent with electrospun nanofibers. Our method allows intrinsically rechargeable N-halamine moieties to covalently incorporate into nanofibers with high biocidal activity and durability. The resulting BNF membranes exhibit integrated properties of high porosity, large surface area, robust mechanical strength, super hydrophilicity, rechargeable chlorination capability (>3000 ppm), and high bactericidal efficacy (99.9999% contact-killing), which enabled the BNF membranes effectively disinfect bacteria-contained water by direct filtration, with promising high durability and fluxes (10000 L m −2 h −1 ). The successful synthesis of BNF membranes also provides a versatile platform for exploring the antimicrobial N-halamine materials in a self-supporting, structurally adaptive, and nanofibrous form.
Titanium dioxide gel monoliths were synthesized using an organic precursor and 0-30 vol % ethanol in water. The visible-light-activated proton pump, bacteriorhodopsin, in its native purple membrane form, was successfully encapsulated within the titanium dioxide gels. Absorption spectra showed that the folded functional state of the protein remained intact within gels made with 0 and 15 vol % ethanol and retained the ability to make reversible conformational changes associated with the photocycle within the gel made with 0 vol % ethanol. The photocatalytic activity of gels made with no ethanol was significantly detectable and gels made with 0-30 vol % ethanol were comparable to commercial crystalline nanoparticles in similar solution conditions when irradiated with UV light. Our results show that sol-gel-derived photocatalytic titanium dioxide can be made biocompatible for a membrane-associated protein by minimizing the amount of ethanol and maximizing the amount of water in the synthesis procedure. The entrapment of the membrane protein, bacteriorhodopsin, in sol-gel-derived titanium dioxide provides the first step in future explorations of this bionanocomposite for visible light photocatalysis, including hydrogen production.
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