Melt direct-spinning online added colored polyester fibers and preparation method thereof
A melt direct spinning, colored polyester technology, applied in the field of polyester fibers, can solve the problems of poor degradation effect and slow degradation rate, and achieve the effect of increasing the degradation rate, increasing the free volume of voids, and improving the natural degradation rate
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0058] The preparation method of adding colored polyester fiber on-line by melt direct spinning, the steps are as follows:
[0059] (1) prepare modified polyester;
[0060] (1.1) prepare 2,5,6,6-tetramethyl-2,5-heptanediol, the synthetic method is:
[0061] (a) Mix KOH powder, 3-methyl-3-hydroxybutyne, 3,3-dimethyl-2-butanone and isopropyl ether at a molar ratio of 1:1:1.2:2.0, and place in an ice bath Under the conditions of reaction for 2h, cooling crystallization, centrifugation, washing, refining and drying are carried out after the reaction to obtain octyne diol;
[0062] (b) Mix octynediol, ethanol and palladium catalyst in a weight ratio of 2:10:0.01, react at a temperature of 40°C for 50 minutes, continuously feed hydrogen during the reaction, and separate and purify after the reaction to obtain 2,5,6,6-tetramethyl-2,5-heptanediol, the structural formula of 2,5,6,6-tetramethyl-2,5-heptanediol is shown in formula (I);
[0063] (1.2) Esterification reaction;
[0064]...
Embodiment 2
[0075] The preparation method of adding colored polyester fiber on-line by melt direct spinning, the steps are as follows:
[0076] (1) prepare modified polyester;
[0077] (1.1) Preparation of 2-tert-butyl-1,6-hexanedicarboxylic acid: firstly mix tungstic acid and hydrogen peroxide, stir at room temperature for 10 minutes, then add 2-tert-butylcyclohexanol and firstly mix at 80°C React for 1 hour, then raise the temperature to 94°C and react for 2 hours. During the reaction, the reactants are always in a reflux state, and finally undergo cooling crystallization, washing and refining. The ratio is 1:35:120;
[0078] (1.2) Preparation of 2,5,6,6-tetramethyl-2,5-heptanediol, the synthesis method is:
[0079] (a) Mix KOH powder, 3-methyl-3-hydroxybutyne, 3,3-dimethyl-2-butanone and isopropyl ether at a molar ratio of 1.1:1:1.2:2.3, and place in an ice bath Under the conditions of reaction for 2h, cooling crystallization, centrifugation, washing, refining and drying are carried...
Embodiment 3
[0089] The preparation method of adding colored polyester fiber on-line by melt direct spinning, the steps are as follows:
[0090] (1) prepare modified polyester;
[0091] (1.1) Preparation of 2-tert-butyl-1,6-hexanedicarboxylic acid: firstly mix tungstic acid and hydrogen peroxide, stir at room temperature for 12 minutes, then add 2-tert-butylcyclohexanol and firstly mix at 83°C React for 1.5 hours, then raise the temperature to 90°C and react for 2 hours. During the reaction, the reactants are always in a reflux state, and finally carry out cooling crystallization, washing and refining. The molar ratio is 1:33:120;
[0092] (1.2) Preparation of 2,5,6,6-tetramethyl-2,5-heptanediol, the synthesis method is:
[0093] (a) Mix KOH powder, 3-methyl-3-hydroxybutyne, 3,3-dimethyl-2-butanone and isopropyl ether at a molar ratio of 1.2:1:1.25:2.0, and place in an ice bath Under the conditions of reaction for 3 hours, after the reaction is completed, cooling and crystallization, ce...
PUM
Property | Measurement | Unit |
---|---|---|
Monofilament denier | aaaaa | aaaaa |
Breaking strength | aaaaa | aaaaa |
Fineness | aaaaa | aaaaa |
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