Nitrogen halamine type antibacterial polyurethane material as well as preparation method and application thereof
A polyurethane material, nitrogen halamine type technology, used in polyurea/polyurethane coatings, textiles and papermaking, antifouling/underwater coatings, etc., can solve the problems of low efficiency, non-persistent and unstable nitrogen halamine type compounds, etc. , to achieve the effect of low cytotoxicity, low price and easy availability, and increased stability
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0036] The present invention also provides a preparation method of nitrogen halide type antibacterial polyurethane material, comprising the following steps:
[0037] S1. Add 10 to 20 parts of guanidine salt, 1 to 5 parts of 2-acetylbutyrolactone, 4 to 11 parts of triethylamine and 15 to 29 parts of absolute ethanol in parts by weight and stir in the reactor for 30 to 60 minutes. React at 70-80°C for 24-48 hours, cool down to room temperature, and rinse with ethanol to obtain nitrogen haloamine precursor A, whose structural formula is:
[0038]
[0039] S2. Add 20 to 30 parts of polyol, 4 to 8 parts of diisocyanate, and 5 to 12 parts of N,N-dimethylformamide into another reactor, and then add 0.002 to 0.004 parts of catalyst. React at ~85°C for 2 to 4 hours to prepare prefabricated material B;
[0040] S3. Add 18-26 parts of N,N-dimethylformamide, 0.4-1.0 parts of chain extender and 0.1-0.6 parts of nitrogen halide to the preform B prepared in S2. The amine precursor A is ...
Embodiment 1
[0048] This embodiment provides a nitrogen halide type antibacterial polyurethane material that can be used in fields such as toy coatings, textile coatings, and medical devices, which is prepared by the following process:
[0049] S1. Add 10 parts of guanidinium carbonate, 2 parts of 2-acetylbutyrolactone, 4 parts of triethylamine, and 20 parts of absolute ethanol into the reactor in parts by weight and stir for 30 minutes, then react at 78°C for 24 hours, After cooling down to room temperature, after rinsing with ethanol, the nitrogen haloamine precursor A is obtained;
[0050]S2. Add 20 parts of polyether N220, 5 parts of aliphatic diisocyanate IPDI, and 7 parts of N,N-dimethylformamide DMF into another reactor, and add 0.002 parts of catalyst to it, and in a nitrogen atmosphere React at 80°C for 2 hours to prepare preform B;
[0051] S3. Add 20 parts of N,N-dimethylformamide DMF, 0.8 parts of chain extender BDO and 0.15 parts of nitrogen haloamine precursor dried under va...
Embodiment 2
[0055] This embodiment provides a nitrogen halide type antibacterial polyurethane material that can be used in fields such as toy coatings, textile coatings, and medical devices, which is prepared by the following process:
[0056] S1. Add 10 parts of guanidinium carbonate, 2 parts of 2-acetylbutyrolactone, 4 parts of triethylamine, and 20 parts of absolute ethanol into the reactor in parts by weight and stir for 30 minutes, then react at 78°C for 24 hours, After cooling down to room temperature, after rinsing with ethanol, the nitrogen haloamine precursor A is obtained;
[0057] S2. Add 20 parts of polyether N220, 5 parts of aliphatic diisocyanate IPDI, and 7 parts of N,N-dimethylformamide DMF into another reactor, and add 0.002 parts of catalyst to it, and in a nitrogen atmosphere React at 80°C for 2 hours to prepare preform B;
[0058] S3. Add 20 parts of N,N-dimethylformamide DMF, 0.8 part of chain extender BDO and 0.2 part of nitrogen haloamine precursor dried under vacu...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com