Red and blue anthraquinone-contained polyphenylene sulfone copolymers and preparation methods and applications thereof

A technology of anthraquinone polyphenylene sulfone and polyphenylene sulfone, which is applied in the field of polyaryl ether sulfone copolymer preparation, can solve the problems of material mechanical performance degradation, dye decomposition, and high energy consumption, and achieve good solubility and Thermal stability, uniform and stable color, and good transparency

Inactive Publication Date: 2013-11-27
JILIN UNIV
View PDF5 Cites 1 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, since the processing temperature of polyarylethersulfone materials is often between 350 and 380°C, it is difficult for traditional organic dye molecules to maintain good thermal stability at this temperature, which will easily cause dye decomposition, resulting in high energy consumption and poor color fastness. Low dyeing efficiency, low mechanical properties of materials and environmental pollution

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
  • Red and blue anthraquinone-contained polyphenylene sulfone copolymers and preparation methods and applications thereof
  • Red and blue anthraquinone-contained polyphenylene sulfone copolymers and preparation methods and applications thereof
  • Red and blue anthraquinone-contained polyphenylene sulfone copolymers and preparation methods and applications thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0035] Add 0.001mol (0.2232g) 1-aminoanthraquinone, 0.020mol (5.0850g) 4,4′-difluorodiphenyl sulfone and 0.0011mol (0.1518g) anhydrous potassium carbonate to a device equipped with mechanical stirring, thermometer, with water In the three-necked flask of the condenser and the condenser, nitrogen protection, 28 mL of sulfolane (TMS) was used as the reaction solvent, the solid content was 20%, and 10 mL of toluene was used as the aqueous agent. Bring water at 140°C for 3 hours, distill out toluene, then gradually heat up from 140°C to 200°C at a rate of 10°C / hour, and stay at 200°C for 2 hours. Heating was stopped, cooled to room temperature, 0.019 mol (3.5380 g) of 4,4'-biphenol and 0.0209 mol (2.8842 g) of anhydrous potassium carbonate were added, and 10 mL of toluene was added again. Bring water at 140°C for 2.5 hours, distill out toluene, then gradually increase the temperature from 140°C to 200°C at a rate of 10°C / hour, and stay at 200°C for 2 hours. Stop heating, when the...

Embodiment 2

[0037] Add 0.003mol (0.6697g) 1-aminoanthraquinone, 0.030mol (7.6275g) 4,4'-difluorodiphenyl sulfone and 0.0033mol (0.4554g) anhydrous potassium carbonate to a device equipped with mechanical stirring, thermometer, with water In the three-necked flask of the condenser and the condenser, nitrogen protection, 43 mL of sulfolane (TMS) was used as the reaction solvent, the solid content was 20%, and 15 mL of toluene was used as the aqueous agent. Bring water at 140°C for 3 hours, distill out toluene, then gradually increase the temperature from 140°C to 210°C at a rate of 10°C / hour, and stay at 210°C for 2 hours. Heating was stopped, cooled to room temperature, 0.019 mol (3.5380 g) of 4,4'-biphenol and 0.0297 mol (2.8842 g) of anhydrous potassium carbonate were added, and 15 mL of toluene was added again. Bring water at 140°C for 3 hours, distill out toluene, then gradually heat up from 140°C to 200°C at a rate of 10°C / hour, and stay at 200°C for 2 hours. Stop heating, when the t...

Embodiment 3

[0039] Combine 0.001mol (0.2702g) 1,5-diamino-4,8-dihydroxyanthraquinone, 0.020mol (5.0850g) 4,4′-difluorodiphenylsulfone and 0.0011mol (0.1518g) anhydrous potassium carbonate Put it into a three-necked flask equipped with a mechanical stirring, a thermometer, a water device and a condenser, nitrogen protection, and use 54 mL of N,N-dimethylacetamide (DMAc) as the reaction solvent, with a solid content of 15%, and 18 mL of toluene as With water. Bring water at 135°C for 3 hours, distill out toluene, then gradually increase the temperature from 135°C to 160°C at a rate of 10°C / hour, and stay at 160°C for 2 hours. Heating was stopped, cooled to room temperature, 0.019 mol (3.5380 g) of 4,4'-biphenol and 0.0209 mol (2.8842 g) of anhydrous potassium carbonate were added, and 18 mL of toluene was added again. Bring water at 135°C for 3 hours, distill out toluene, then gradually increase the temperature from 135°C to 160°C at a rate of 10°C / hour, and stay at 160°C for 2 hours. Sto...

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
thermal decomposition temperatureaaaaaaaaaa
thermal decomposition temperatureaaaaaaaaaa
glass transition temperatureaaaaaaaaaa
Login to view more

Abstract

The invention discloses red and blue anthraquinone-contained polyphenylene sulfone copolymers and preparation methods and applications thereof, belongs to the technical field of preparation of polyether sulfone copolymers, and in particular relates to red and blue anthraquinone-contained polyphenylene sulfone copolymers and preparation methods thereof, and the applications of red and blue anthraquinone-contained polyphenylene sulfone copolymers in the dying of pure polyphenylene sulfone. According to the preparation methods, 4,4'-difluoro diphenyl sulfone, 4,4'-biphenyl diphenol and 1-aminoanthraquinone or 1,5-diamido-4,8-dihydroxy anthraquinone are employed as raw materials, a nucleophilic polycondensation method is employed to introduce anthraquinone chromophoric molecules with high thermal stability into a polyphenylene sulfone system in a covalent bond manner, thus the novel red and blue anthraquinone-contained polyphenylene sulfone copolymers with anthraquinone content of 1%-30% and thermal decomposition temperature of more than 500 DEG C can be prepared. The series of polymers have high molecular weight, good solubility and heat stability, and meanwhile have intrinsic red and blue colors and good transparency.

Description

technical field [0001] The invention belongs to the technical field of preparation of polyaryl ether sulfone copolymers, in particular to a red and blue anthraquinone-containing polyphenylene sulfone copolymer, a preparation method and its application in dyeing pure polyphenylene sulfone application. Background technique [0002] Polyphenylene sulfone (PPSU) material has comprehensive properties such as high heat resistance, chemical corrosion resistance, good dimensional stability, and excellent electrical properties. application. With the broadening of application fields, in addition to basic thermal and mechanical properties, the requirements for materials in terms of appearance, color, energy conservation and environmental protection are also gradually increasing. [0003] Industrially, for polyarylethersulfone materials including polyphenylene sulfone, the traditional dyeing methods are high temperature and high pressure dyeing method, carrier dyeing method and hot me...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C08G75/23C08L81/06C08J3/22
Inventor 姜振华崔曾多张海博朱晔路遥平姜波
Owner JILIN UNIV
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