2008
DOI: 10.1016/j.reactfunctpolym.2007.09.004
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Biocidal polymers (I): Preparation and biological activity of some novel biocidal polymers based on uramil and its azo-dyes

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Cited by 55 publications
(40 citation statements)
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“…N-halamines can be applied to various textile surfaces including cellulose [25][26][27], polyamide [28] and polyester [29] fibers. To increase their effectiveness and the durability of the antimicrobial finish [25], research has been oriented toward synthesis of N-halamide monomers with an incorporated vinyl reactive group ( Figure 3) [30,31] that can polymerize on cellulose fibers under appropriate conditions to form a coating with excellent durability after washing [30]. …”
Section: N-halaminesmentioning
confidence: 99%
“…N-halamines can be applied to various textile surfaces including cellulose [25][26][27], polyamide [28] and polyester [29] fibers. To increase their effectiveness and the durability of the antimicrobial finish [25], research has been oriented toward synthesis of N-halamide monomers with an incorporated vinyl reactive group ( Figure 3) [30,31] that can polymerize on cellulose fibers under appropriate conditions to form a coating with excellent durability after washing [30]. …”
Section: N-halaminesmentioning
confidence: 99%
“…The product was filtered, washed with 100 ml distilled water, and dried (6). The amount of halogen loaded on the polymer was determined by using iodometric titration, at 115 Ϯ 20 ppm (2,22).…”
Section: Materials M-phenylenediaminementioning
confidence: 99%
“…Polymer 2 (1 g) was soaked in 20 ml sodium hypochlorite (7.5%, wt/wt) overnight. The polymer was filtered, washed with distilled water (100 ml), and dried at 45°C for 24 h. The amount of halogen on the polymer was determined by using iodometric titration (2,22). The polymer was heated in 20 ml sodium thiosulfate (0.01 M) at 45°C for 1 h and then filtered, washed with halogen-free water, and dried at 45°C for 24 h. The polymer was rehalogenated using sodium hypochlorite, and the halogen was then removed with sodium thiosulfate (the process was repeated four times, charging with halogen and then discharging with sodium thiosulfate), and in each case, the amount of halogen loaded onto the polymer was determined.…”
Section: Materials M-phenylenediaminementioning
confidence: 99%
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“…Two methods can be used for this purpose: impregnation of the antibacterial agent on the polymeric support or chemical modification of the polymer [1][2][3][4][5][6][7][8][9][10] . Alternatively, monomers containing the bactericidal groups can be polymerized and subsequently cross-linked to obtain a biocidal polymer [9,[11][12][13] . Although polymerization of functionalized monomers is a more direct route to prepare biocidal polymers, these functionalized monomers are expensive and it is hard to obtain spherical beads with controlled morphology.…”
Section: Introductionmentioning
confidence: 99%