Abstract

ABSTRACTTo reduce the neutral salt used in the textile finishing with s‐triazine derivatives, a novel s‐triazine‐based quaternarized N‐halamine precursor was synthesized by two simple steps and characterized by H‐NMR and FT‐IR. This compound can be effectively coated onto cellulose by nucleophilic substitution process without neutral salt. The treated cellulose was rendered with powerful biocidal efficacy after transferring to an N‐halamine structure by exposing to dilute sodium hypochlorite solution through the synergistic antimicrobial effect quaternary ammonium salt and N‐halamine. The chlorinated samples could inactivate 6‐logs of Staphylococcus aureus and Escherichia coli O157:H7 within 1 min and 5 min, respectively. In addition, about 50% of oxidant chlorine remained after 50 washing cycles and 30 days storage, and all of the lost active chlorines in the N‐halamine molecules recovered after exposing to bleach solution. With these advantages, the as‐prepared antimicrobial fabrics will have potential application, especially in the medical and healthcare textiles. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 44998.

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