[1] KOVACIC P, LOWERY M K. Chemistry of N-halamines. XII. Amination of alkyl halides with trichloramine-aluminum chloride[J]. The Journal of Organic Chemistry, 1969, 34(4): 911-917. [2] KOVACIC P, LOWERY M K, FIELD K W. Chemistry of N-bromamines and N-chloramines[J]. Chemical Reviews, 1970, 70(6): 639-665. [3] SUN G, WHEATLEY W B, WORLEY S D. A new cyclic N-halamine biocidal polymer[J]. Industrial & Engineering Chemistry Research, 1994, 33(1): 168-170. [4] HUI F, DEBIEMME-CHOUVY C. Antimicrobial N-halamine polymers and coatings: A review of their synthesis, characterization, and applications[J]. Biomacromolecules, 2013, 14(3): 585-601. [5] LI L, JUNG J, MA W, et al. Enhanced antimicrobial and antifungal property of two-dimensional fibrous material assembled by N-halamine polymeric electrolytes[J]. Materials Science and Engineering C, 2020, 115: 111122. [6] SUN X, CAO Z, PORTEOUS N, et al. Amine, melamine, and amide N-halamines as antimicrobial additives for polymers[J]. Industrial & Engineering Chemistry Research, 2010, 49(22): 11206-11213. [7] REN X H, KOU L, KOCER H B, et al. Antimicrobial coating of an N-halamine biocidal monomer on cotton fibers via admicellar polymerization[J]. Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2008, 317(1/2/3): 711-716. [8] WORLRY S D, WILLAMS D E, CRAWFROD R A. Halamine water disinfectants[J]. Critical Reviews in Enviromental Control, 1988, 18(2): 133-175. [9] REN X H, KOCER H B, WORLEY S D, et al. Rechargeable biocidal cellulose: Synthesis and application of 3-(2,3-dihydroxypropyl)-5,5-dimethylimidazolidine-2,4-dione[J]. Carbohydrate Polymers, 2009, 75(4): 683-687. [10] BARNELA S B, WORLEY S D, WILLAMS D E. Syntheses and antibacterial activity of new N-halamine compounds[J]. Journal of Pharmaceutical Sciences, 1987, 76(3): 245-247. [11] AHMED A E S I, HAY J N, BUSHELL M E, et al. Optimizing halogenation conditions of N-halamine polymers and investigating mode of bactericidal action[J]. Journal of Applied Polymer Science, 2009, 113(4): 2404-2412. [12] CHOI K, NAM M J, KIM J Y, et al. Synthesis and characterization of biocidal poly(oxyethylene)s having N-halamine side groups[J]. Macromolecular Research, 2011, 19(12): 1227-1232. [13] EKNOIAN M W, WORLEY S D, Harris J M. New biocidal N-halamine-PEG polymers[J]. Journal of Bioactive and Compatible Polymers, 1998, 13(2): 136-145. [14] REN X H, AKDAG A, ZHU C Y, et al. Electrospun polyacrylonitrile nanofibrous biomaterials [J]. Journal of Biomedical Materials Research Part A, 2009, 91A(2): 385-390. [15] LEE J, BROUGHTON R M, AKDAG A, et al. Preparation and application of ans-triazine-based novel N-halamine biocide for antimicrobial fibers[J]. Fibers and Polymers, 2007, 8(2): 148-154. [16] LIANG J, CHEN Y J, REN X H, et al. Fabric treated with antimicrobial N-halamine epoxides[J]. Industrial & Engineering Chemistry Research, 2007, 46(20): 6425-6429. [17] LI L, MA K K, LIU Y, et al. Biocompatible antimicrobial cotton modified with tricarbimide-based N-halamine [J]. Polymers for Advanced Technologies, 2014, 25(9): 963-968. [18] MA K K, LIU Y, XIE Z, et al. Synthesis of novel N-halamine epoxide based on cyanuric acid and its application for antimicrobial finishing [J]. Industrial & Engineering Chemistry Research, 2013, 52(22): 7413-7418. [19] PASTORIZA C, ANTELO J M, CRUGEIRAS J. Reactions of chlorination withtert-butyl hypochlorite (TBuOCl)[J]. Journal of Physical Organic Chemistry, 2014, 27(12): 952-959. [20] PASTORIZA C, ANTELO J M, CRUGEIRAS J. Use of N-chloro-N-methyl-p-toluenesulfonamide in N-chlorination reactions[J]. Journal of Physical Organic Chemistry, 2013, 26(7): 551-559. [21] BADROSSAMAY M R, SUN G. Acyclic halamine polypropylene polymer: Effect of monomer structure on grafting efficiency, stability and biocidal activities[J]. Reactive and Functional Polymers, 2008, 68(12): 1636-1645. [22] LUO J, SUN Y. Acyclic N-halamine-based fibrous materials: Preparation, characterization, and biocidal functions [J]. Journal of Polymer Science Part A Polymer Chemistry, 2006, 44(11): 3588-3600. [23] YLDIZ O, CERKEZ I, KOCER H B, et al. N-(hydroxymethyl)acrylamide as a multifunctional finish to cotton and a tether for grafting methacrylamide for biocidal coatings[J]. Journal of Applied Polymer Science, 2013, 128(6): 4405-4410. [24] DUTTA A K, EGUSA M, KAMINAKA H, et al. Facile preparation of surface N-halamine chitin nanofiber to endow antibacterial and antifungal activities[J]. Carbohydrate Polymers, 2015, 115: 342-347. [25] CAO Z, SUN Y. N-halamine-based chitosan: Preparation, characterization, and antimicrobial function[J]. Journal of Biomedical Materials Research Part A, 2008, 85(1): 99-107. [26] LI R, HU P, REN X H, et al. Antimicrobial N-halamine modified chitosan films[J]. Carbohydrate Polymers, 2013, 92(1): 534-539. [27] CHENG X L, MA K K, LI R, et al. Antimicrobial coating of modified chitosan onto cotton fabrics[J]. Applied Surface Science, 2014, 309: 138-143. [28] HUGANG C, CHEN Y B, SUN G, et al. Disinfectant performance of a chlorine regenerable antibacterial microfiber fabric as a reusable wiper[J]. Materials, 2019, 12(1): 127. [29] TAMIZIFAR M, SUN G. Control of surface radical graft polymerization on polyester fibers by using Hansen solubility parameters as a measurement of the affinity of chemicals to materials[J]. RSC Advances, 2017, 7(22): 13299-13303. [30] TAMIZIFAR M, SUN G. Surface modification of poly(ethylene terephthalate)fibers via controlled radical graft polymerization[J]. Journal of Applied Polymer Science, 2018, 135(11): 45990. [31] TAMIZIFAR M, SUN G. Controlled surface function-alization of poly(ethylene terephthalate)fibers with varied vinyl monomers via radical graft copolymerization[J]. Materials Today Communications, 2018, 17: 124-132. [32] XI G H, XIUY L, WANG L, et al. Antimicrobial N-halamine coatings synthesized via vapor-phase assisted polymerization[J]. Journal of Applied Polymer Science, 2015, 132(15): 41824. [33] ANDOU Y, JEONG J M, NISHIDA H, et al. Simple procedure for polystyrene-based nanocomposite preparation by vapor-phase-assisted surface polymerization[J]. Macromolecules, 2009, 42(20): 7930-7935. [34] ANDOU Y, JEONG J M, HIKI S, et al. Design of nanocomposites by vapor-phase assisted surface polymeri-zation[J]. Macromolecules, 2009, 42(3): 768-772. [35] 王留阳,王芳颖.卤胺在织物抗菌改性中的应用进展[J].上海纺织科技,2011,39(11):8-11. WANG Liuyang, WANG Fangying. Progress of halamine applications in the preparation of antimicrobial fabrics[J]. Shanghai Textile Science & Technology, 2011, 39(11): 8-11. [36] LIU S, ZHAO N, RUDENJA S. Surface interpenetrating networks of poly(ethylene terephthalate)and polyamides for effective biocidal properties[J]. Macromolecular Chemistry and Physics, 2010, 211(3): 286-296. [37] ZHAO N, ZHANEL G G, LIU S. Regenerability of antibacterial activity of interpenetrating polymeric N-halamine and poly(ethylene terephthalate)[J]. Journal of Applied Polymer Science, 2011, 120(1): 611-622. [38] ZHAO N, LIU S. Thermoplastic semi-IPN of polypropylene (PP)and polymeric N-halamine for efficient and durable antibacterial activity[J]. European Polymer Journal, 2011, 47(8): 1654-1663. [39] LIU Y, QIAO M, LV C, et al. N-halamine polyelectrolytes used for preparation of antibacterial polypropylene nonwoven fabrics and study on their basal cytotoxicity and mutagenicity[J]. International Journal of Polymeric Materials and Polymeric Biomaterials, 2020, 69(15): 971-978. [40] LIU Y, LI J, CHENG X, et al. Self-assembled antibacterial coating by N-halamine polyelectrolytes on a cellulose substrate[J]. Journal of Materials Chemistry B, 2015, 3(7): 1446-1454. [41] DENIS-ROHR A, BASTARRACHEA L J, GODDARD J M. Antimicrobial efficacy of N-halamine coatings prepared via dip and spray layer-by-layer deposition[J]. Food and Bioproducts Processing, 2015, 96: 12-19. [42] CERKEZ I, WORLEY S D, BROUGHTON R M, et al. Antimicrobial coatings for polyester and polyester/cotton blends[J]. Progress in Organic Coatings, 2013, 76(7/8): 1082-1087. [43] CERKEZ I, KOCER H B, WOLEY S D, et al. Antimicrobial functionalization of poly(ethylene terephthalate)fabrics with waterborne N-halamine epoxides[J]. Journal of Applied Polymer Science, 2016, 133(9): 43088. [44] CERKEZ I, WOLEY S D, BROUGHTON R M, et al. Antimicrobial surface coatings for polypropylene nonwoven fabrics[J]. Reactive and Functional Polymers, 2013, 73(11): 1412-1419. [45] 张淑敏,任学宏,李清芳.卤胺抗菌共聚物改性丙纶无纺布的研究[J].化工新型材料,2018,46(4): 201-204. ZHANG Shumin, REN Xuehong, LI Qingfang. Study on antibacterial finishing of PP nonwoven fabric by N-halamine copolymer[J]. New Chemical Materials, 2018, 46(4): 201-204. [46] DEMIR B, CERKEZ I, WORLEY S D, et al. N-halamine-modified antimicrobial polypropylene nonwoven fabrics for use against airborne bacteria[J]. ACS Applied Materials & Interfaces, 2015, 7(3): 1752-1757. [47] CHEN Y, HE Q K, REN G Y, et al. Preparation of biocidal 4-ethyl-4-(hydroxymethyl)oxazolidin-2-one-based N-halamine polysiloxane for impregnation of polypropylene in supercritical CO2[J]. Journal of Applied Polymer Science, 2018, 135(33): 46624. [48] 李蓉,刘喆,任学宏.环状卤胺化合物改性壳聚糖/PVA纳米纤维的制备与表征[J].材料导报,2013,27(14):45-48. LI Rong, LIU Zhe, REN Xuehong. Preparation and characterization of cyclic N-halamine modified chitosan/PVA nanofibers[J]. Materials Reports, 2013, 27(14): 45-48. [49] 黄程博,任学宏.静电纺抗菌聚丙烯腈纳米纤维膜制备及其性能[J].纺织学报,2019,40(5):7-11. HUANG Chengbo, REN Xuehong. Synthesis and properties of antibacterial polyacrylonitrile nanofiber membrane[J]. Journal of Textile Research, 2019, 40(5): 7-11. [50] HUANG C B, LIU Y, LI Z G, et al. N-halamine antibacterial nanofibrous mats based on polyacrylonitrile and N-halamine for protective face masks[J]. Journal of Engineered Fibers and Fabrics, 2019, 14: 1-8. [51] LUO H, YIN X Q, TAN P F, et al. Engineering an antibacterial nanofibrous membrane containing N-halamine for recyclable wound dressing application[J]. Materials Today Communications, 2020, 23: 100898. [52] BAI R, ZHANG Q, LI L L, et al. N-halamine-containing electrospun fibers kill bacteria via a contact/release co-determined antibacterial pathway[J]. ACS Applied Materials & Interfaces, 2016, 8(46): 31530-31540. [53] TIAN CC, WU F, JIAO W L, et al. Antibacterial and antiviral N-halamine nanofibrous membranes with nanonet structure for bioprotective applications[J]. Composites Communications, 2021, 24: 100668. [54] BADROSSAMAY M R, SUN G. A study of radical graft copolymerization on polypropylene during extrusion using two peroxide initiators[J]. Polymer International, 2010, 59(2): 155-161. [55] BADROSSAMAY M R, SUN G. A study on melt grafting of N-halamine moieties onto polyethylene and their antibacterial activities[J]. Macromolecules, 2009, 42(6): 1948-1954. [56] BADROSSAMAY M R, SUN G. Graft polymerization of N-tert-butylacrylamide onto polypropylene during melt extrusion and biocidal properties of its products[J]. Polymer Engineering & Science, 2009, 49(2): 359-368. [57] BADROSSAMAY M R, SUN G. Durable and rechargeable biocidal polypropylene polymers and fibers prepared by using reactive extrusion[J]. Journal of Biomedical Materials Research Part B Applied Biomaterials, 2009, 89B(1): 93-101. [58] BADROSSAMAY M R, SUN G. Preparation of rechargeable biocidal polypropylene by reactive extrusion with diallylamino triazine[J]. European Polymer Journal, 2008, 44(3): 733-742. [59] WANG D, SUN G, CHIOU B S. A high-throughput, controllable, and environmentally benign fabrication process of thermoplastic nanofibers[J]. Macromolecular Materials and Engineering, 2007, 292(4): 407-414. [60] WANG D, LIU N, XU W L, et al. Layer-by-layer structured nanofiber membranes with photoinduced self-cleaning functions[J]. The Journal of Physical Chemistry C, 2011, 115(14): 6825-6832. [61] WANG D, SUN G. Formation and morphology of cellulose acetate butyrate (CAB)/polyolefin and CAB/polyester in situ microfibrillar and lamellar hybrid blends[J]. European Polymer Journal, 2007, 43(8): 3587-3596. [62] WANG D, XU W L, SUN G, et al. Radical graft polymerization of an allyl monomer onto hydrophilic polymers and their antibacterial nanofibrous membranes[J]. ACS Applied Materials & Interfaces, 2011, 3(8): 2838-2844. |