Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

A kind of polyimide fiber and preparation method thereof

A technology of polyimide fiber and polyamic acid fiber, applied in the field of fibers, can solve the problems of easy agglomeration, poor heat aging resistance, large specific surface area of ​​nanoparticles, etc.

Active Publication Date: 2021-04-27
CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
View PDF8 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The main problem of the method of adding anti-ultraviolet nanoparticles is that the nanoparticles have a large specific surface area and are easy to agglomerate, so the dispersion of the nanoparticles in the matrix is ​​difficult to control, the processing repeatability is poor, and it affects the product's resistance to ultraviolet radiation; the method of adding small organic molecules The main problem is that organic small molecules have poor thermal aging resistance, and they will decompose and lose under high temperature conditions, resulting in poor mechanical properties of materials, reducing or even losing the anti-ultraviolet radiation performance of materials.

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
  • A kind of polyimide fiber and preparation method thereof
  • A kind of polyimide fiber and preparation method thereof
  • A kind of polyimide fiber and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0053] The invention provides a kind of preparation method of polyimide fiber, comprises the following steps:

[0054] a) Aromatic dianhydride monomers and diamine monomers are polymerized in a solvent to obtain a polyamic acid spinning stock solution;

[0055] b) spinning the polyamic acid spinning stock solution to obtain polyamic acid fibers;

[0056] c) performing imidization treatment on the polyamic acid fibers to obtain polyimide fibers;

[0057] The diamine monomer comprises monomer A and monomer B;

[0058] The monomer A is selected from one or more of the structures shown in formula a-1 to formula a-8:

[0059]

[0060] The monomer B is selected from one or more of the structures shown in formula b-1 to formula b-7:

[0061]

[0062] in,

[0063] M is selected from -O-, -S-, or -NH-;

[0064]X is selected from -O-, -S-, or -NH-;

[0065] D is selected from -O-, -S-, or -NH-;

[0066] E is selected from -O-, -S-, -SO 2 -, -CH 2 -, -C(CF 3 ) 2 -, -CO-,...

preparation example 1

[0203] Raw material preparation example 1 Preparation of diamine shown in monomer A-formula a-1

[0204] (1) 69.52 grams (0.56 moles) of 3-methoxyphenol, 88.23 grams (0.56 moles) of p-nitrochlorobenzene, 85.14 grams (0.616 moles) of potassium carbonate and 200 grams of dimethyl sulfoxide were added to the reactor in sequence , heated to 160°C for 6 hours; cooled to 60°C, added to 2000 ml of water, the crude product was precipitated, filtered out, washed with water, dissolved in dichloromethane, dried over anhydrous magnesium sulfate, and concentrated to obtain the crude product 114.23 grams of refined product of compound (II-1) represented by formula (II) were obtained through recrystallization; the yield was 83.2%.

[0205] Utilize nuclear magnetic resonance to characterize the structural compound (II-1) shown in the formula (II) that obtains, the proton nuclear magnetic resonance spectrum result that obtains is: 1 H NMR (400MHz, DMSO) δ = 8.280–8.205 (m, 2H), 7.389 (t, J = 8....

preparation example 2

[0212] Raw material preparation example 2 Preparation of diamine shown in monomer A-formula a-2

[0213] (1) 62.07 grams (0.50 moles) of 3-methoxyphenol, 101.0 grams (0.50 moles) of m-bromonitrobenzene, 4.76 grams (0.025 moles) of cuprous iodide, 76.02 grams (0.55 moles) of potassium carbonate and 200 Add grams of N,N-dimethylformamide to the reaction flask in turn, heat the reaction system to 150°C under nitrogen protection and react for 12 hours; after cooling to 60°C, add it to 2000 ml of water, precipitate the crude product, filter it out, and wash with water Afterwards, it was dissolved in dichloromethane, dried over anhydrous magnesium sulfate, the solvent was concentrated, and purified to obtain 90.59 g of the refined product of the structural compound (II-2) shown in formula (II); the yield was 73.9%.

[0214] (2) 89.07 grams (0.48 moles) of 4-nitrobenzoyl chloride, 69.34 grams (0.52 moles) of aluminum trichloride, 1000 milliliters of dichloromethane and 105.45 grams (...

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
heightaaaaaaaaaa
Login to View More

Abstract

The invention provides a polyimide fiber and a preparation method thereof. The polyimide fiber provided by the present invention and the preparation method thereof comprise the following steps: a) polymerizing the aromatic dianhydride monomer and the diamine monomer in a solvent to obtain a polyamic acid spinning stock solution; b) making the polyamide Spinning the acid spinning stock solution to obtain polyamic acid fibers; c) imidizing the polyamic acid fibers to obtain polyimide fibers; the diamine monomers include monomer A and monomer B; the monomer A is selected from one or more of the structures of formula a-1 to formula a-8 shown below; the monomer B is selected from the structures of formula b-1 to formula b-7 shown below one or more of them. In the present invention, the specific monomer A containing o-hydroxybenzophenone structural units in the main chain is matched with the monomer B as a diamine monomer, polymerized and spun with a dianhydride monomer to obtain polyimide fibers, and the specific monomer The introduction of can improve the UV aging resistance of polyimide.

Description

technical field [0001] The invention relates to the field of fiber technology, in particular to a polyimide fiber and a preparation method thereof. Background technique [0002] Polyimide fiber material is a new type of special fiber with excellent comprehensive properties. The molecular chain contains imide rings. It has many excellent properties such as high strength, high modulus, high temperature resistance, flame retardancy, chemical corrosion resistance, and low temperature resistance. Performance, widely used in aerospace, weapons and equipment, transportation and other high-tech fields. [0003] During the use of polyimide fiber materials, its performance will be affected by the environment, especially after ultraviolet radiation, chemical reactions will occur on the surface of the fiber, resulting in a decrease in the performance of the fiber. In particular, polyimide fiber materials used in aerospace vehicles, without the barrier of the high-altitude atmosphere (e...

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 Patents(China)
IPC IPC(8): D01F6/78C08G73/10
CPCC08G73/1042C08G73/1071D01F6/78
Inventor 姚海波董志鑫刘芳芳代学民李国民王汉夫邱雪鹏
Owner CHANGCHUN INST OF APPLIED CHEMISTRY - CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products