Journal
CELLULOSE
Volume 30, Issue 6, Pages 3473-3488Publisher
SPRINGER
DOI: 10.1007/s10570-023-05095-x
Keywords
Biocidal surface; N-chloramine; Quaternary ammonium salt; Synergism; Cotton cellulose; Supercritical CO2
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A highly efficient biocide and an easily applicable procedure are two keys for antibacterial modification of cotton cellulose. A quaternized di-N-chloramine silicone that contains complementary functionalities of one quaternary ammonium salt (QAS) and two N-chloramine sites (an amidic one and an imidic one) in each composite unit was synthesized to better contact with bacteria to exert super biocidability.
A highly efficient biocide and an easily applicable procedure are two keys for antibacterial modification of cotton cellulose. A quaternized di-N-chloramine silicone that contains complementary functionalities of one quaternary ammonium salt (QAS) and two N-chloramine sites (an amidic one and an imidic one) in each composite unit was synthesized to better contact with bacteria to exert super biocidability. Briefly, Knoevenagel condensation between hydantoin with 4-dimethylaminobenzaldehyde produced a compound with one amidic and one imidic nitrogens and one tertiary amine. The tertiary amine of the Knoevenagel product was quaternized with 3-chloro-1-propanol whose hydroxyl group was subsequently bonded to poly(methylhydrosiloxane) via silane alcoholysis. The silane alcoholysis product was interpenetrated into cotton cellulose at 50 degrees C and 28 MPa in supercritical CO2 (scCO(2)) and its amidic and imidic nitrogens were then chlorinated to form a 76 nm quaternized di-N-chloramine silicone layer. Biocidal assay proved that QAS and N-chloramine sites functioned synergistically, eliminating similar to 7 log of S. aureus and E. coli at a much faster rate (in 3 min) than each functionality. The scCO(2) interpenetration produced a durable modification layer as shown by stability tests without the reliance upon chemical linkages and hence can be transferable to substrates with different components.
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