[go: up one dir, main page]

Peng et al., 2021 - Google Patents

Fabrication of N-halamine polyurethane films with excellent antibacterial properties

Peng et al., 2021

View HTML
Document ID
8215623635846058993
Author
Peng P
Yang J
Wu Q
Wu M
Liu J
Zhang J
Publication year
Publication venue
e-Polymers

External Links

Snippet

An N-halamine precursor, namely, 2-amino-5-(2-hydroxyethyl)-6-methylpyrimidin-4-one (AHM), was used as a chain extender in the preparation of a series of N-halamine polyurethane (PU) films, in order to also instill antibacterial properties. The mechanical …
Continue reading at www.degruyterbrill.com (HTML) (other versions)

Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G
    • C08J3/00—Processes of treating or compounding macromolecular substances
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION, OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS, OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS, OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G
    • C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION, OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS, OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS, OR SURGICAL ARTICLES
    • A61L15/00—Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16—Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42—Use of materials characterised by their function or physical properties

Similar Documents

Publication Publication Date Title
Chen et al. Hydrogen-bond assembly of poly (vinyl alcohol) and polyhexamethylene guanidine for nonleaching and transparent antimicrobial films
Chen et al. Novel poly (vinyl alcohol)/chitosan/modified graphene oxide biocomposite for wound dressing application
Li et al. Bioinspired dual-crosslinking strategy for fabricating soy protein-based adhesives with excellent mechanical strength and antibacterial activity
Lizundia et al. Synergic effect of nanolignin and metal oxide nanoparticles into poly (l-lactide) bionanocomposites: material properties, antioxidant activity, and antibacterial performance
Abdeen et al. Nanocomposite framework of chitosan/polyvinyl alcohol/ZnO: Preparation, characterization, swelling and antimicrobial evaluation
Wang et al. Superior performance of polyurethane based on natural melanin nanoparticles
Li et al. Transparent and ultra-tough PVA/alkaline lignin films with UV shielding and antibacterial functions
Li et al. Robust protein hydrogels from silkworm silk
Dhand et al. Multifunctional polyphenols-and catecholamines-based self-defensive films for health care applications
Wang et al. IPN hydrogel nanocomposites based on agarose and ZnO with antifouling and bactericidal properties
Zhang et al. Tough and strong biomimetic soy protein films with excellent UV-shielding performance
Wang et al. A facile method for processing lignin reinforced chitosan biopolymer microfibres: optimising the fibre mechanical properties through lignin type and concentration
Liu et al. Nonwoven supported temperature‐sensitive poly (N‐isopropylacrylamide)/polyurethane copolymer hydrogel with antibacterial activity
Kodsangma et al. Effect of sodium benzoate and chlorhexidine gluconate on a bio-thermoplastic elastomer made from thermoplastic starch-chitosan blended with epoxidized natural rubber
Raju et al. Chitosan-terephthaldehyde hydrogels–Effect of concentration of cross-linker on structural, swelling, thermal and antimicrobial properties
Yin et al. Facile fabrication of sandwich structural membrane with a hydrogel nanofibrous mat as inner layer for wound dressing application
Si et al. Mechanically robust and transparent N‐halamine grafted PVA‐co‐PE films with renewable antimicrobial activity
Maamoun et al. Exploring the mechanical and bacterial prospects of flexible polyurethane foam with chitosan
Cao et al. Surface enrichment and nonleaching antimicrobial performance of polypropylene grafted poly (hexamethylene guanidine)(PP-g-PHMG) in poly (ethylene terephthalate)/PP-g-PHMG
Wang et al. A cross-linking/percolating-integrated strategy to enhance crystallizable rubber using rod-like reactive biobased nanocrystals
Chen et al. Intensifying the antimicrobial activity of poly [2-(tert-butylamino) ethyl methacrylate]/polylactide composites by tailoring their chemical and physical structures
Yu et al. Nanoclay Reinforced Self‐Cross‐Linking Poly (N‐Hydroxyethyl Acrylamide) Hydrogels with Integrated High Performances
Peng et al. Fabrication of N-halamine polyurethane films with excellent antibacterial properties
Yu et al. β-Lactamase responsive supramolecular hydrogels with host–guest self-healing capability
Yang et al. Highly stretchable gamma-irradiated poly (vinyl alcohol)/Tannic acid composite hydrogels with superior transparency and antibacterial activity