Dihydric alcohol modified polyester fibers with trimethylsilyl lateral groups and preparation method thereof

A technology of trimethylsilyl and modified polyester, which is applied in the direction of fiber chemical characteristics, single-component polyester rayon, rayon manufacturing, etc., which can solve the problems of inability to catalyze, high cost, graying of polyester color and brightness reduction, etc. problem, to achieve the effect of increasing the free volume of space and changing the interaction force

Active Publication Date: 2019-05-07
JIANGSU HENGLI CHEM FIBER
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, due to the compact structure and high crystallinity of PET, the natural degradation time is very long (the degradation cycle of conventional polyester fibers can reach 16-48 years), which greatly limits the application of chemical degradation and recycling in the field of PET waste treatment.
In addition, at this stage, common antimony-based catalysts on the market such as Sb 2 o 3 The amount added in the polyester synthesis process is large, and the large amount of antimony-based catalysts has a greater impact on the environment, which is not conducive to the environmental protection production of polyester. At the same time, the antimony-based catalysts will be converted into antimony in the polycondensation reaction. , so that the gray color and brightness of polyester are reduced, the greater the amount of antimony-based catalyst added, the greater the impact on the color and quality of polyester, but the antimony-based catalyst added in a small amount cannot react to all the raw materials involved in polyester synthesis. Catalysis, unable to meet the needs of polyester production
[0004] In addition, because polyester is a hydrophobic fiber, its molecules do not contain hydrophilic groups, and its molecular structure lacks active groups that can combine with dyes like cellulose or protein fibers, so the dyeing performance of polyester fibers is not good.
In addition, the finished polyester fiber has a partially crystalline supramolecular structure, and its crystalline molecular chains are parallel to each other, mostly in a trans conformation, while the amorphous region is mostly in a cis conformation, and its molecules are arranged quite closely, which further increases the polyester Fiber Dyeing Difficulty
At present, conventional polyester (PET) fibers are generally dyed with disperse dyes at high temperature (130°C) and high pressure. Only dyeing at high temperature and high pressure can ensure the dyeing rate of the fiber, and high temperature and high pressure have high requirements for equipment and low energy consumption. At the same time, due to the difficulty of dyeing, the time required for dyeing is longer, resulting in higher cost of the process, which limits the application of colorful polyester fibers to a certain extent
Although there are methods such as chemical modification in the prior art, such as by introducing the third or fourth component for copolymerization, or by introducing functional groups with different characteristics, or improving the affinity of polyester macromolecules to dyes The dyeing performance of polyester fiber, but it may have limited improvement on the dyeing performance of the fiber, or the preparation technology is complicated and uncontrollable, or the modification method has a great influence on other properties of the fiber such as mechanical properties

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Dihydric alcohol modified polyester fibers with trimethylsilyl lateral groups and preparation method thereof
  • Dihydric alcohol modified polyester fibers with trimethylsilyl lateral groups and preparation method thereof
  • Dihydric alcohol modified polyester fibers with trimethylsilyl lateral groups and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0080] A preparation method of glycol-modified polyester fibers with trimethylsilyl side groups, the steps are as follows:

[0081] (1) Preparation of doped modified Sb 2 o 3 ;

[0082] (1.1) Mg(NO 3 ) 2 aqueous solution with a concentration of 8 mol% Sb 2 o 3 The solution is mixed evenly, Sb 2 o 3 The solvent of the solution is oxalic acid, the Mg in the mixture 2+ with Sb 3+ The molar ratio is 2:100;

[0083] (1.2) Add dropwise ammonia water with a concentration of 2 mol / L until the pH value of the mixed solution is 9 to obtain a precipitated product, and then wash and dry the precipitated product at a temperature of 105° C. for 2.5 hours;

[0084] (1.3) The dried product was first heated to 400°C and then kept for 2.5h, then heated to 900°C and kept for 1.5h, and finally cooled in air and pulverized to obtain doped modified Sb with an average particle size of 0.4 microns 2 o 3 Powder;

[0085] (2) Preparation of doped modified Bi 2 o 3 Powder;

[0086] (2.1)...

Embodiment 2

[0104] A preparation method of glycol-modified polyester fibers with trimethylsilyl side groups, the steps are as follows:

[0105] (1) Preparation of doped modified Sb 2 o 3 ;

[0106] (1.1) The concentration of 0.5mol% Ca(NO 3 ) 2 Aqueous solution with a concentration of 5 mol% Sb 2 o 3 The solution is mixed evenly, Sb 2 o 3 The solvent of the solution is oxalic acid, the Ca in the mixture 2+ with Sb 3+ The molar ratio is 1:100;

[0107] (1.2) Add dropwise ammonia water with a concentration of 2 mol / L until the pH value of the mixed solution is 10 to obtain a precipitated product, and then wash and dry the precipitated product at a temperature of 110° C. for 2 hours;

[0108] (1.3) The dried product was first heated to 400°C and then kept for 2h, then heated to 900°C and kept for 1h, and finally cooled in air and pulverized to obtain doped modified Sb with an average particle size of 0.4 microns 2 o 3 Powder;

[0109] (2) Preparation of doped modified Bi 2 o 3...

Embodiment 3

[0124] A preparation method of glycol-modified polyester fibers with trimethylsilyl side groups, the steps are as follows:

[0125] (1) Preparation of doped modified Sb 2 o 3 ;

[0126] (1.1) Ba(NO 3 ) 2 Aqueous solution with a concentration of 10 mol% Sb 2 o 3 The solution is mixed evenly, Sb 2 o 3 The solvent of the solution is oxalic acid, Ba in the mixture 2+ with Sb 3+ The molar ratio is 3:100;

[0127] (1.2) Add dropwise ammonia water with a concentration of 2 mol / L until the pH of the mixed solution is 9.5 to obtain a precipitated product, and then wash and dry the precipitated product at a temperature of 105° C. for 3 hours;

[0128] (1.3) The dried product was first heated to 400°C and kept for 3 hours, then heated to 900°C and kept for 2 hours, and finally cooled in air and pulverized to obtain doped modified Sb with an average particle size of 0.5 microns 2 o 3 Powder;

[0129] (2) Preparation of doped modified Bi 2 o 3 Powder;

[0130] (2.1) The con...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
Monofilament denieraaaaaaaaaa
Breaking strengthaaaaaaaaaa
Monofilament denieraaaaaaaaaa
Login to view more

Abstract

The invention relates to dihydric alcohol modified polyester fibers with trimethylsilyl lateral groups and a preparation method thereof. Dihydric alcohol modified polyester melts with the trimethylsilyl lateral groups are metered, extruded out through a spinneret plate, cooled, oiled and wound to prepare the dihydric alcohol modified polyester fibers with trimethylsilyl lateral groups, dihydric alcohol chain segments with trimethylsilyl lateral groups are introduced into molecular chains of dihydric alcohol modified polyester with trimethylsilyl lateral groups, and the structural formula of the chain segments is shown in the specification, wherein R is -CH2- or -CH(CH3)-or -C[(CH3)2]-, and doping modification Bi2O3 powder and doping modification Sb2O3 powder are dispersed in the dihydric alcohol modified polyester with trimethylsilyl lateral groups. The method is simple in technology, and the dihydric alcohol modified polyester fibers with trimethylsilyl lateral groups is good in dyeing performance, high in natural degrading efficiency and quite good in popularization value.

Description

technical field [0001] The invention belongs to the technical field of modified fibers, and relates to a glycol-modified polyester fiber with trimethylsilyl side groups and a preparation method thereof. Background technique [0002] Polyester is the trade name of polyester fiber in my country, and it is an important variety in synthetic fibers. It is a fiber-forming high polymer prepared from purified terephthalic acid (PTA) or dimethyl terephthalate (DMT) and ethylene glycol (EG) through esterification or transesterification and polycondensation reactions. Polyethylene terephthalate (PET), a fiber made by spinning and post-processing. Polyester fiber not only has good heat resistance, chemical resistance, mechanical properties and electrical properties, but also has the advantages of good transparency, good insulation, low production cost and high cost performance. [0003] However, with the rapid development of the PET industry, although PET will not directly cause harm ...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): D01F6/92D01F1/10C08G63/695C08G63/86C08G63/83
Inventor 孙晓华陈瑞汤方明
Owner JIANGSU HENGLI CHEM FIBER
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap