A kind of method of synthesizing polyacrylonitrile copolymer

A technology for polyacrylonitrile and copolymers, which is applied in the field of synthesizing polyacrylonitrile copolymers, which can solve the problems of unfavorable increase in the molecular weight of polyacrylonitrile products, difficult control, cumbersome process, etc., and achieves reduced transfer probability, easy heat dissipation, and simple operation Effect

Active Publication Date: 2022-04-08
HENAN UNIV OF URBAN CONSTR
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Judging from the reaction status, the former reaction is relatively moderate, and there is a transfer reaction to the small molecular chain, which is beneficial to reduce the branching of the macromolecular chain, but is not conducive to increasing the molecular weight of the polyacrylonitrile product.
Compared with the homogeneous solution polymerization system, the latter uses water as the reaction medium entirely, and there is no chain transfer reaction to the solvent, so a higher molecular weight polyacrylonitrile copolymer can be produced, but its reaction is more violent and difficult to control, and its Polymerization products need to be filtered, washed, dried, dissolved to make spinning solution, and then degassed before they can be used for spinning. The process is relatively cumbersome

Method used

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  • A kind of method of synthesizing polyacrylonitrile copolymer
  • A kind of method of synthesizing polyacrylonitrile copolymer
  • A kind of method of synthesizing polyacrylonitrile copolymer

Examples

Experimental program
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Effect test

Embodiment 1

[0023] The present embodiment provides a kind of method for synthesizing polyacrylonitrile copolymer, concrete steps comprise:

[0024] In a 250ml flask, first add 0.264g ammonium persulfate and 0.66g itaconic acid, 32.34g acrylonitrile monomer, 114.66g dimethyl sulfoxide, 2.34g deionized water, mix and dissolve evenly to obtain a solution to be polymerized, and then Move the flask into a constant temperature water bath at 65°C, use magnetic stirring, and react for 4 hours under the protection of nitrogen to obtain a uniform transparent viscous liquid; figure 1 As shown, the homogeneous transparent viscous liquid is transparent.

[0025] After the reaction is over, remove the flask from the water bath and add cold water to terminate the polymerization reaction. The obtained polymer solution is pressed into a film, soaked and dried to obtain a polyacrylonitrile copolymer. The appearance of the polyacrylonitrile copolymer is shown in the figure figure 2 Shown, its conversion r...

Embodiment 2

[0027] The present embodiment provides a kind of method for synthesizing polyacrylonitrile copolymer, concrete steps comprise:

[0028] In a 250ml flask, first add 0.198g of ammonium persulfate and 0.66g of itaconic acid, then add 32.34g of acrylonitrile monomer, 109.98g of dimethyl sulfoxide, and 7.02g of deionized water, mix and dissolve evenly, and then move the flask into Put it in a constant temperature water bath at 58°C, use magnetic stirring, and react for 4 hours under the protection of nitrogen to obtain a uniform transparent viscous liquid; image 3 As shown, the homogeneous transparent viscous liquid is transparent.

[0029] After the reaction is over, the flask is removed from the water bath and cold water is added to terminate the polymerization reaction, and the obtained polymer solution is pressed into a film, soaked and dried to obtain a polyacrylonitrile copolymer. Its conversion rate is 80% after testing.

Embodiment 3

[0031] The present embodiment provides a kind of method for synthesizing polyacrylonitrile copolymer, concrete steps comprise:

[0032] In a 250ml flask, first add 0.33g of azobisisobutylamidine hydrochloride and 0.66g of itaconic acid, then add 32.34g of acrylonitrile monomer, 111.15g of dimethylformamide, and 5.85g of deionized water. After mixing and dissolving evenly, the flask was moved into a constant temperature water bath at 65°C, stirred by magnetic force, and reacted for 6 hours under the protection of nitrogen.

[0033] After the reaction is over, the flask is removed from the water bath and cold water is added to terminate the polymerization reaction, and the obtained polymer solution is pressed into a film, soaked and dried to obtain a polyacrylonitrile copolymer. Its conversion rate was tested to be 51%.

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Abstract

The invention provides a method for synthesizing a polyacrylonitrile copolymer. First, a solid water-soluble initiator and a solid comonomer are added to a mixed solvent composed of an organic solvent and deionized water, and then propylene is added to the mixed solvent The nitrile main monomer and the liquid comonomer are mixed evenly to obtain a solution to be polymerized; wherein, the mass fraction of deionized water in the mixed solvent is greater than 0% and less than 10%; the solution to be polymerized is placed in a constant temperature water bath at 50°C to 70°C Magnetic stirring is carried out in the medium to generate a polymerization reaction, and a uniform transparent viscous liquid is obtained, and the uniform transparent viscous liquid is sequentially subjected to film pressing, soaking, washing, and drying to obtain a polyacrylonitrile copolymer. The polymerization solution prepared by this method is transparent, and can be directly used for spinning after only single removal and defoaming without dissolution process, especially compared to the heterogeneous polymerization process for preparing high molecular weight polyacrylonitrile copolymers. Processes such as filtration, washing, drying, and dissolution are omitted, which is beneficial to actual industrial production.

Description

technical field [0001] The invention belongs to the technical field of chemical industry, in particular to a method for synthesizing polyacrylonitrile copolymers. Background technique [0002] Carbon fiber is a high-performance material with a carbon content of over 90%. Carbon fiber has excellent properties such as high tensile strength, high elastic modulus, high temperature stability and low density. The excellent performance of carbon fiber determines its wide application in civil and military fields. Among them, polyacrylonitrile fiber is the most potential precursor for the production of carbon fiber. The carbon fiber prepared by pre-oxidation, carbonization and graphitization has excellent comprehensive performance, and the production process is relatively simple, the technology is relatively mature, and the cost is relatively low. The widest range of carbon fiber products. [0003] In order to produce high-quality and high-strength polyacrylonitrile-based carbon fi...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08F220/46C08F222/02C08F220/14D01F6/38
CPCC08F220/46D01F6/38C08F222/02C08F220/14
Inventor 赵亚奇冯巧郭雯静梁浜雷李辉周梦珂杜玲枝赵振新赵海鹏郭靖怡
Owner HENAN UNIV OF URBAN CONSTR
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