Polyamide with sulfonic acid group
A technology of sulfonic acid groups and polyamides, applied in the field of polyamides, can solve the problems of lack of dyeing fastness of cationic dyes, etc.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0024] Add 2g of 5-sulfosalicylic acid, 2.1g of polyvinylpyrrolidone and a catalyst to 40g of polybutylene adipamide, heat to melt under a nitrogen atmosphere, gradually raise the temperature to 90°C, and react at a constant temperature for 2 hours. Then gradually raise the temperature to 260°C, and react at constant temperature for 3h. The polymer was decanted from the reaction vessel and soaked several times with sufficient distilled water to remove unreacted monomer. After drying in a vacuum drying oven for 24 hours, it was melt spun at a spinning speed of 600 m / min to obtain easily dyed fibers. The dyeing properties of the fibers are listed in Table 1.
Embodiment 2
[0026] Add 5g of 2-amino-5-sulfobenzoic acid, 0.9g of polyvinylpyrrolidone and a catalyst to 40g of polyhexamethylene dodecanediamide, heat it to melt under a nitrogen atmosphere, and gradually raise the temperature to 120°C. Constant temperature reaction 1h. Then gradually raise the temperature to 280° C., and react at constant temperature for 4 hours. The polymer was decanted from the reaction vessel and soaked several times with sufficient distilled water to remove unreacted monomer. After drying in a vacuum drying oven for 24 hours, it was melt spun at a spinning speed of 600 m / min to obtain easily dyed fibers. The dyeing properties of the fibers are listed in Table 1.
Embodiment 3
[0028] Add 2g of 5-sulfosalicylic acid, 1g of polyvinylpyrrolidone and a catalyst to 40g of 11-aminoundecanoic acid, add an appropriate amount of distilled water, and heat to 200°C for 3 hours at a constant temperature under a nitrogen atmosphere. Then the temperature was gradually increased to 270 °C, and the reaction was carried out at constant temperature for 6 h. The polymer was decanted from the reaction vessel and soaked several times with sufficient distilled water to remove unreacted monomer. After drying in a vacuum drying oven for 24 hours, it was melt spun at a spinning speed of 600 m / min to obtain easily dyed fibers. The dyeing properties of the fibers are listed in Table 1.
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