CN113430680A - Graphene-carbon composite fiber prepared from graphene-itaconic acid monomer and preparation method thereof - Google Patents
Graphene-carbon composite fiber prepared from graphene-itaconic acid monomer and preparation method thereof Download PDFInfo
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- 239000002131 composite material Substances 0.000 title claims abstract description 101
- 239000000178 monomer Substances 0.000 title claims abstract description 71
- 239000000835 fiber Substances 0.000 title claims abstract description 67
- 229910052799 carbon Inorganic materials 0.000 title claims abstract description 63
- 238000002360 preparation method Methods 0.000 title abstract description 11
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 81
- 229910021389 graphene Inorganic materials 0.000 claims abstract description 72
- 238000003763 carbonization Methods 0.000 claims abstract description 67
- 229920000049 Carbon (fiber) Polymers 0.000 claims abstract description 59
- 239000004917 carbon fiber Substances 0.000 claims abstract description 59
- 238000000034 method Methods 0.000 claims abstract description 55
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims abstract description 54
- 230000003647 oxidation Effects 0.000 claims abstract description 49
- 238000007254 oxidation reaction Methods 0.000 claims abstract description 49
- 239000002243 precursor Substances 0.000 claims abstract description 49
- 229920000642 polymer Polymers 0.000 claims abstract description 46
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims abstract description 45
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims abstract description 43
- 239000002904 solvent Substances 0.000 claims abstract description 35
- 238000009987 spinning Methods 0.000 claims abstract description 34
- 239000003505 polymerization initiator Substances 0.000 claims abstract description 33
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 29
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims abstract description 28
- 238000011065 in-situ storage Methods 0.000 claims abstract description 17
- 230000001681 protective effect Effects 0.000 claims abstract description 15
- 238000002156 mixing Methods 0.000 claims abstract description 10
- 239000000243 solution Substances 0.000 claims description 18
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 16
- 238000006243 chemical reaction Methods 0.000 claims description 16
- 239000003999 initiator Substances 0.000 claims description 15
- 150000003254 radicals Chemical group 0.000 claims description 15
- 230000014759 maintenance of location Effects 0.000 claims description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 12
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims description 10
- 239000006185 dispersion Substances 0.000 claims description 10
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 239000007789 gas Substances 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 125000000524 functional group Chemical group 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 5
- 235000019400 benzoyl peroxide Nutrition 0.000 claims description 5
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 4
- 239000011259 mixed solution Substances 0.000 claims description 4
- 238000009210 therapy by ultrasound Methods 0.000 claims description 2
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- 229920000297 Rayon Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 239000011157 advanced composite material Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
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- 238000012824 chemical production Methods 0.000 description 1
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- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000012377 drug delivery Methods 0.000 description 1
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- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
- D01F9/08—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material
- D01F9/12—Carbon filaments; Apparatus specially adapted for the manufacture thereof
- D01F9/14—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments
- D01F9/20—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products
- D01F9/21—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D01F9/22—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyacrylonitriles
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/44—Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/56—Polymerisation initiated by wave energy or particle radiation by ultrasonic vibrations
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/42—Nitriles
- C08F220/44—Acrylonitrile
- C08F220/46—Acrylonitrile with carboxylic acids, sulfonic acids or salts thereof
-
- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
Abstract
The invention discloses a graphene-carbon composite fiber prepared from a graphene-itaconic acid monomer and a preparation method thereof, wherein the method comprises the following steps: step 1, mixing graphene oxide, an acrylonitrile monomer, an itaconic acid monomer, a solvent and a polymerization initiator to perform ultrasonic-assisted in-situ polymerization, and preparing a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer to obtain a composite spinning solution; step 2, spinning the composite spinning solution into composite protofilaments after demonomerization and defoaming; and 3, carrying out pre-oxidation treatment on the composite protofilament, and carrying out carbonization treatment in a protective atmosphere to obtain the graphene-carbon composite fiber. The invention also provides a graphene-itaconic acid monomer for the PAN polymer as the precursor of the carbon fiber prepared by the method, and a graphene-carbon composite fiber prepared by the graphene-itaconic acid monomer. The graphene-carbon composite fiber prepared by the method has excellent mechanical properties, and the graphene has an obvious reinforcing effect on carbon fibers.
Description
Technical Field
The invention relates to a graphene-carbon composite fiber prepared from a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer and a preparation method thereof, and particularly relates to a graphene-carbon composite fiber prepared from a graphene-itaconic acid monomer and a preparation method thereof.
Background
As a new high-speed material which is developed rapidly in recent years, graphene has excellent optical, electrical and mechanical properties, has important application prospects in the aspects of materials science, micro-nano processing, energy, biomedicine, drug delivery and the like, and is considered to be a revolutionary material in the future. Graphene is a single-layer carbon atom material stripped from graphite, and a single-layer two-dimensional honeycomb lattice structure is formed by tightly packing carbon atoms, and is known to be the material with the thinnest thickness, the hardest texture and the best conductivity. Graphene has excellent mechanical, optical and electrical properties and a very stable structure, researchers have not found that graphene has a missing carbon atom, the linkage between carbon atoms is very flexible, and is harder than diamond, the strength is 100 times higher than that of the world's best steel, if graphene is used for making a packaging bag, the graphene can bear about two tons of articles, the graphene is almost completely transparent, but is very compact, waterproof and airtight, helium gas with the minimum atomic size cannot pass through the graphene, the graphene has good conductivity, the movement speed of electrons in graphene reaches 1/300 of the light speed, the conductivity exceeds that of any traditional conductive material, the chemical properties are similar to the surface of graphite, various atoms and molecules can be adsorbed and desorbed, and the graphene also has the capability of resisting strong acid and strong alkali.
The carbon fiber is a special fiber consisting of carbon elements, and is a high-strength high-modulus fiber with the carbon content of more than 90 percent. The graphite fiber has the characteristics of high temperature resistance, friction resistance, electric conduction, heat conduction, corrosion resistance and the like, is fibrous and soft in appearance, can be processed into various fabrics, and has high strength and modulus along the fiber axis direction due to the preferred orientation of the graphite microcrystalline structure along the fiber axis. The carbon fibers have a low density and thus a high specific strength and a high specific modulus. The carbon fiber is mainly used as a reinforcing material to be compounded with resin, metal, ceramic, carbon and the like to manufacture an advanced composite material. The specific strength and the specific modulus of the carbon fiber reinforced epoxy resin composite material are the highest in the existing engineering materials.
The carbon fiber is generally made from acrylic fiber and viscose fiber as raw materials and is oxidized and carbonized at high temperature, the high temperature resistance of the carbon fiber is the first of all chemical fibers, and the carbon fiber is an excellent material for manufacturing high-technology equipment such as aerospace and aviation. The graphene is used in the production and processing of carbon fibers, so that the comprehensive performance of the carbon fibers can be further improved.
Disclosure of Invention
The invention aims to provide a graphene-carbon composite fiber prepared from a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer and a preparation method thereof.
In order to achieve the above object, the present invention provides a method for preparing a graphene-carbon composite fiber from a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer, wherein the method comprises: step 1, mixing graphene oxide, an acrylonitrile monomer, an itaconic acid monomer, a solvent and a polymerization initiator to perform ultrasonic-assisted in-situ polymerization, and preparing a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer to obtain a composite spinning solution; step 2, the composite spinning solution obtained in the step 1 is demonomerized and defoamed, and then is spun into composite protofilaments; and 3, carrying out pre-oxidation treatment on the composite protofilament obtained in the step 2, and then carrying out carbonization treatment in a protective atmosphere to obtain the graphene-carbon composite fiber.
The method for preparing the graphene-carbon composite fiber through the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer comprises the following steps of 1, wherein the mass ratio of graphene oxide, itaconic acid, an acrylonitrile monomer, a polymerization initiator and a solvent is (0.1-15): (1-12): (15-25): (0.15-0.75): 100.
the method for preparing the graphene-carbon composite fiber through the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer comprises the following steps of (1-30): 100, respectively; the average value of the graphene oxide sheet diameter is 3-7 mu m, and the average number of layers is less than or equal to 10.
The method for preparing the graphene-carbon composite fiber from the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer comprises the following steps of.
The method for preparing the graphene-carbon composite fiber from the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer comprises the following steps of (1) preparing a carbon fiber precursor PAN polymer by using a polymerization initiator; the adopted free radical initiator is any one of azobisisobutyronitrile, azobisisoheptonitrile, dibenzoyl peroxide and tert-butyl hydroperoxide.
The method for preparing the graphene-carbon composite fiber from the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer comprises the following steps of mixing a solvent and a solvent, and then adding the solvent into the mixture to prepare the carbon fiber precursor PAN polymer.
The method for preparing the graphene-carbon composite fiber through the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer comprises the steps of performing ultrasonic-assisted in-situ polymerization in the step 1, wherein the mixed solution containing graphene oxide, itaconic acid, acrylonitrile, a solvent and a polymerization initiator is subjected to ultrasonic treatment at room temperature for 1-2 hours, then heating to 40-70 ℃ for reaction for 10-30 hours, and performing ultrasonic enhancement on uniform dispersion of the graphene oxide in a polymerization system in the first 1-5 hours of the reaction.
The method for preparing the graphene-carbon composite fiber from the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer comprises the step 3, wherein the pre-oxidation treatment is carried out in air by adopting a gradient temperature raising method, the initial temperature of the pre-oxidation treatment is 80-230 ℃, the final temperature of the pre-oxidation treatment is 260-300 ℃, the pre-oxidation treatment is carried out on the composite precursor in 2-6 temperature zones, and the total time of the pre-oxidation treatment is 25-100 minutes.
The method for preparing the graphene-carbon composite fiber through the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer comprises the steps of low-temperature carbonization and high-temperature carbonization, wherein the carbonization treatment in the step 3 comprises low-temperature carbonization and high-temperature carbonization, high-purity nitrogen is used as a shielding gas for both the low-temperature carbonization and the high-temperature carbonization, the low-temperature carbonization temperature is 350-1000 ℃, the retention time is 1-10 minutes, and then the high-temperature carbonization is carried out, the temperature is 1100-1500 ℃, and the retention time is 0.5-5 minutes.
The invention also provides the graphene-itaconic acid monomer for the PAN polymer as the precursor of the carbon fiber prepared by the method and the graphene-carbon composite fiber prepared by the graphene-itaconic acid monomer.
The graphene-carbon composite fiber prepared from the graphene-itaconic acid monomer and the preparation method thereof provided by the invention have the following advantages:
the graphene-carbon composite fiber obtained by the method has excellent mechanical properties, and compared with the existing preparation method of polyacrylonitrile-based carbon fiber, the tensile strength of the graphene-carbon composite fiber obtained by the method is improved by 20-50%, the tensile modulus is improved by 9-50%, and meanwhile, the preparation method has the characteristics of simple process, easiness in industrial production and the like.
The invention solves the problems of dispersion of graphene in the fiber and chemical bonding with a carbon network structure in the fiber, so that the graphene has an obvious reinforcing effect on the carbon fiber. The diameter of the prepared graphene-carbon composite fiber is 7-10 mu m, the tensile strength is 6-9 GPa, and the tensile modulus is 250-400 GPa.
Detailed Description
The following further describes embodiments of the present invention.
The invention provides a method for preparing graphene-carbon composite fiber by using a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer, which comprises the following steps:
step 1, mixing graphene oxide, an acrylonitrile monomer, an itaconic acid monomer, a solvent and a polymerization initiator to perform ultrasonic-assisted in-situ polymerization, and preparing the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer to obtain a composite spinning solution.
PAN, polyacrylonitrile (polyacrylonitrile), is a chemical substance obtained by radical polymerization of acrylonitrile, a monomer. The itaconic acid is known as methylene succinic acid and itaconic acid, is unsaturated binary organic acid, contains unsaturated double bond, has active chemical property, can carry out polymerization among the itaconic acid and the itaconic acid, can also carry out polymerization with other monomers such as acrylonitrile and the like, can carry out various addition reactions, esterification reactions and polymerization reactions, is an important raw material in chemical synthesis industry, and is also an important raw material in chemical production.
And 2, demonomerizing and defoaming the composite spinning solution obtained in the step 1, and then preparing the composite protofilament through a spinning process.
The processes and parameters adopted by demonomerization, defoaming and spinning are all the prior art choices in the field. The demonomerization and the defoaming are to remove residual volatile monomers in the acrylonitrile polymerization solution and remove bubbles contained in the spinning solution before spinning so as to ensure that the subsequent spinning process can be normally carried out.
And 3, carrying out pre-oxidation treatment on the composite protofilament obtained in the step 2, and then carrying out carbonization treatment in a protective atmosphere to obtain the graphene-carbon composite fiber.
Preferably, in the step 1, the mass ratio of the graphene oxide, the itaconic acid, the acrylonitrile monomer, the polymerization initiator and the solvent is (0.1-15): (1-12): (15-25): (0.15-0.75): 100.
the ratio of the number of oxygen-containing functional groups in the graphene oxide to the number of carbon atoms in the graphene oxide is (1-30): 100, respectively; the average value of the graphene oxide sheet diameter is 3-7 mu m, and the average number of layers is less than or equal to 10.
Itaconic acid is analytically pure itaconic acid.
The polymerization initiator is a free radical initiator; the adopted free radical initiator is any one of azobisisobutyronitrile, azobisisoheptonitrile, dibenzoyl peroxide and tert-butyl hydroperoxide.
The solvent is any one of dimethyl sulfoxide, dimethylformamide, dimethylacetamide and cyclobuterol.
The ultrasonic-assisted in-situ polymerization in the step 1 is to ultrasonically treat a mixed solution containing graphene oxide, itaconic acid, acrylonitrile, a solvent and a polymerization initiator for 1-2 hours at room temperature, then heat the mixed solution to 40-70 ℃ for reaction for 10-30 hours, and ultrasonically enhance the uniform dispersion of the graphene oxide in a polymerization system in the first 1-5 hours of the reaction.
And (3) carrying out pre-oxidation treatment in the step 3 by adopting a gradient temperature raising method in the air, wherein the initial temperature of the pre-oxidation treatment is 80-230 ℃, the final temperature of the pre-oxidation treatment is 260-300 ℃, and the pre-oxidation treatment is carried out on the composite precursor in 2-6 temperature zones, and the total time of the pre-oxidation treatment is 25-100 minutes.
And the carbonization treatment in the step 3 comprises a low-temperature carbonization step and a high-temperature carbonization step, wherein high-purity nitrogen is adopted as a protective gas for both the low-temperature carbonization step and the high-temperature carbonization step, the low-temperature carbonization temperature is 350-1000 ℃, the residence time is 1-10 minutes, and then the high-temperature carbonization step is carried out, the temperature is 1100-1500 ℃, and the residence time is 0.5-5 minutes.
The invention also provides a graphene-itaconic acid monomer for the PAN polymer as the precursor of the carbon fiber prepared by the method, and a graphene-carbon composite fiber prepared by the graphene-itaconic acid monomer.
The graphene-carbon composite fiber prepared from the graphene-itaconic acid monomer and the preparation method thereof according to the present invention will be further described with reference to the following examples.
Example 1
A method of preparing a graphene-carbon composite fiber from a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer, comprising:
step 1, mixing graphene oxide, an acrylonitrile monomer, an itaconic acid monomer, a solvent and a polymerization initiator to perform ultrasonic-assisted in-situ polymerization, and preparing the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer to obtain a composite spinning solution.
Preferably, the mass ratio of the graphene oxide, the itaconic acid, the acrylonitrile monomer, the polymerization initiator and the solvent is 0.1: 1: 15: 0.15: 100.
the ratio of the number of oxygen-containing functional groups in the graphene oxide to the number of carbon atoms in the graphene oxide is (1-30): 100, respectively; the average value of the graphene oxide sheet diameter is 3-7 mu m, and the average number of layers is less than or equal to 10.
Itaconic acid is analytically pure itaconic acid.
The polymerization initiator is a free radical initiator; the radical initiator used is azobisisobutyronitrile. The solvent is dimethyl sulfoxide.
The ultrasonic-assisted in-situ polymerization is to ultrasonically treat mixed liquid containing graphene oxide, itaconic acid, acrylonitrile, a solvent and a polymerization initiator for 1-2 hours at room temperature, then heat the mixed liquid to 40-70 ℃ for reaction for 10-30 hours, and perform ultrasonic enhancement on uniform dispersion of the graphene oxide in a polymerization system in the first 1-5 hours of the reaction.
And 2, demonomerizing and defoaming the composite spinning solution obtained in the step 1, and then preparing the composite protofilament through a spinning process.
The processes and parameters adopted by demonomerization, defoaming and spinning are all the prior art choices in the field.
And 3, carrying out pre-oxidation treatment on the composite protofilament obtained in the step 2, and then carrying out carbonization treatment in a protective atmosphere to obtain the graphene-carbon composite fiber.
The pre-oxidation treatment is carried out in the air by adopting a gradient temperature raising method, the initial temperature of the pre-oxidation treatment is 80-230 ℃, the final temperature of the pre-oxidation treatment is 260-300 ℃, the pre-oxidation treatment is carried out on the composite protofilaments in 2-6 temperature zones, and the total time of the pre-oxidation treatment is 25-100 minutes.
The carbonization treatment comprises a low-temperature carbonization part and a high-temperature carbonization part, wherein high-purity nitrogen is used as a protective gas for both the low-temperature carbonization and the high-temperature carbonization, the low-temperature carbonization temperature is 350-1000 ℃, the retention time is 1-10 minutes, and then the high-temperature carbonization is carried out, the temperature is 1100-1500 ℃, and the retention time is 0.5-5 minutes.
The embodiment also provides the graphene-itaconic acid monomer for the PAN polymer as the precursor of the carbon fiber prepared by the method, and the graphene-carbon composite fiber prepared by the graphene-itaconic acid monomer.
Example 2
A method of preparing a graphene-carbon composite fiber from a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer, comprising:
step 1, mixing graphene oxide, an acrylonitrile monomer, an itaconic acid monomer, a solvent and a polymerization initiator to perform ultrasonic-assisted in-situ polymerization, and preparing the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer to obtain a composite spinning solution.
Preferably, the mass ratio of the graphene oxide, the itaconic acid, the acrylonitrile monomer, the polymerization initiator and the solvent is 3: 2: 18: 0.3: 100.
the ratio of the number of oxygen-containing functional groups in the graphene oxide to the number of carbon atoms in the graphene oxide is (1-30): 100, respectively; the average value of the graphene oxide sheet diameter is 3-7 mu m, and the average number of layers is less than or equal to 10.
Itaconic acid is analytically pure itaconic acid.
The polymerization initiator is a free radical initiator; the radical initiator used is azobisisoheptonitrile. The solvent is dimethylformamide.
The ultrasonic-assisted in-situ polymerization is to ultrasonically treat mixed liquid containing graphene oxide, itaconic acid, acrylonitrile, a solvent and a polymerization initiator for 1-2 hours at room temperature, then heat the mixed liquid to 40-70 ℃ for reaction for 10-30 hours, and perform ultrasonic enhancement on uniform dispersion of the graphene oxide in a polymerization system in the first 1-5 hours of the reaction.
And 2, demonomerizing and defoaming the composite spinning solution obtained in the step 1, and then preparing the composite protofilament through a spinning process.
The processes and parameters adopted by demonomerization, defoaming and spinning are all the prior art choices in the field.
And 3, carrying out pre-oxidation treatment on the composite protofilament obtained in the step 2, and then carrying out carbonization treatment in a protective atmosphere to obtain the graphene-carbon composite fiber.
The pre-oxidation treatment is carried out in the air by adopting a gradient temperature raising method, the initial temperature of the pre-oxidation treatment is 80-230 ℃, the final temperature of the pre-oxidation treatment is 260-300 ℃, the pre-oxidation treatment is carried out on the composite protofilaments in 2-6 temperature zones, and the total time of the pre-oxidation treatment is 25-100 minutes.
The carbonization treatment comprises a low-temperature carbonization part and a high-temperature carbonization part, wherein high-purity nitrogen is used as a protective gas for both the low-temperature carbonization and the high-temperature carbonization, the low-temperature carbonization temperature is 350-1000 ℃, the retention time is 1-10 minutes, and then the high-temperature carbonization is carried out, the temperature is 1100-1500 ℃, and the retention time is 0.5-5 minutes.
The embodiment also provides the graphene-itaconic acid monomer for the PAN polymer as the precursor of the carbon fiber prepared by the method, and the graphene-carbon composite fiber prepared by the graphene-itaconic acid monomer.
Example 3
A method of preparing a graphene-carbon composite fiber from a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer, comprising:
step 1, mixing graphene oxide, an acrylonitrile monomer, an itaconic acid monomer, a solvent and a polymerization initiator to perform ultrasonic-assisted in-situ polymerization, and preparing the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer to obtain a composite spinning solution.
Preferably, the mass ratio of the graphene oxide, the itaconic acid, the acrylonitrile monomer, the polymerization initiator and the solvent is 7: 6: 20: 0.45: 100.
the ratio of the number of oxygen-containing functional groups in the graphene oxide to the number of carbon atoms in the graphene oxide is (1-30): 100, respectively; the average value of the graphene oxide sheet diameter is 3-7 mu m, and the average number of layers is less than or equal to 10.
Itaconic acid is analytically pure itaconic acid.
The polymerization initiator is a free radical initiator; the radical initiator used is dibenzoyl peroxide. The solvent is dimethylacetamide.
The ultrasonic-assisted in-situ polymerization is to ultrasonically treat mixed liquid containing graphene oxide, itaconic acid, acrylonitrile, a solvent and a polymerization initiator for 1-2 hours at room temperature, then heat the mixed liquid to 40-70 ℃ for reaction for 10-30 hours, and perform ultrasonic enhancement on uniform dispersion of the graphene oxide in a polymerization system in the first 1-5 hours of the reaction.
And 2, demonomerizing and defoaming the composite spinning solution obtained in the step 1, and then preparing the composite protofilament through a spinning process.
The processes and parameters adopted by demonomerization, defoaming and spinning are all the prior art choices in the field.
And 3, carrying out pre-oxidation treatment on the composite protofilament obtained in the step 2, and then carrying out carbonization treatment in a protective atmosphere to obtain the graphene-carbon composite fiber.
The pre-oxidation treatment is carried out in the air by adopting a gradient temperature raising method, the initial temperature of the pre-oxidation treatment is 80-230 ℃, the final temperature of the pre-oxidation treatment is 260-300 ℃, the pre-oxidation treatment is carried out on the composite protofilaments in 2-6 temperature zones, and the total time of the pre-oxidation treatment is 25-100 minutes.
The carbonization treatment comprises a low-temperature carbonization part and a high-temperature carbonization part, wherein high-purity nitrogen is used as a protective gas for both the low-temperature carbonization and the high-temperature carbonization, the low-temperature carbonization temperature is 350-1000 ℃, the retention time is 1-10 minutes, and then the high-temperature carbonization is carried out, the temperature is 1100-1500 ℃, and the retention time is 0.5-5 minutes.
The embodiment also provides the graphene-itaconic acid monomer for the PAN polymer as the precursor of the carbon fiber prepared by the method, and the graphene-carbon composite fiber prepared by the graphene-itaconic acid monomer.
Example 4
A method of preparing a graphene-carbon composite fiber from a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer, comprising:
step 1, mixing graphene oxide, an acrylonitrile monomer, an itaconic acid monomer, a solvent and a polymerization initiator to perform ultrasonic-assisted in-situ polymerization, and preparing the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer to obtain a composite spinning solution.
Preferably, the mass ratio of the graphene oxide, the itaconic acid, the acrylonitrile monomer, the polymerization initiator and the solvent is 12: 10: 22: 0.6: 100.
the ratio of the number of oxygen-containing functional groups in the graphene oxide to the number of carbon atoms in the graphene oxide is (1-30): 100, respectively; the average value of the graphene oxide sheet diameter is 3-7 mu m, and the average number of layers is less than or equal to 10.
Itaconic acid is analytically pure itaconic acid.
The polymerization initiator is a free radical initiator; the radical initiator used is tert-butyl hydroperoxide. The solvent is cyclobuterol.
The ultrasonic-assisted in-situ polymerization is to ultrasonically treat mixed liquid containing graphene oxide, itaconic acid, acrylonitrile, a solvent and a polymerization initiator for 1-2 hours at room temperature, then heat the mixed liquid to 40-70 ℃ for reaction for 10-30 hours, and perform ultrasonic enhancement on uniform dispersion of the graphene oxide in a polymerization system in the first 1-5 hours of the reaction.
And 2, demonomerizing and defoaming the composite spinning solution obtained in the step 1, and then preparing the composite protofilament through a spinning process.
The processes and parameters adopted by demonomerization, defoaming and spinning are all the prior art choices in the field.
And 3, carrying out pre-oxidation treatment on the composite protofilament obtained in the step 2, and then carrying out carbonization treatment in a protective atmosphere to obtain the graphene-carbon composite fiber.
The pre-oxidation treatment is carried out in the air by adopting a gradient temperature raising method, the initial temperature of the pre-oxidation treatment is 80-230 ℃, the final temperature of the pre-oxidation treatment is 260-300 ℃, the pre-oxidation treatment is carried out on the composite protofilaments in 2-6 temperature zones, and the total time of the pre-oxidation treatment is 25-100 minutes.
The carbonization treatment comprises a low-temperature carbonization part and a high-temperature carbonization part, wherein high-purity nitrogen is used as a protective gas for both the low-temperature carbonization and the high-temperature carbonization, the low-temperature carbonization temperature is 350-1000 ℃, the retention time is 1-10 minutes, and then the high-temperature carbonization is carried out, the temperature is 1100-1500 ℃, and the retention time is 0.5-5 minutes.
The embodiment also provides the graphene-itaconic acid monomer for the PAN polymer as the precursor of the carbon fiber prepared by the method, and the graphene-carbon composite fiber prepared by the graphene-itaconic acid monomer.
Example 5
A method of preparing a graphene-carbon composite fiber from a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer, comprising:
step 1, mixing graphene oxide, an acrylonitrile monomer, an itaconic acid monomer, a solvent and a polymerization initiator to perform ultrasonic-assisted in-situ polymerization, and preparing the graphene-itaconic acid monomer for the carbon fiber precursor PAN polymer to obtain a composite spinning solution.
Preferably, the mass ratio of the graphene oxide, the itaconic acid, the acrylonitrile monomer, the polymerization initiator and the solvent is 15: 12: 25: 0.75: 100.
the ratio of the number of oxygen-containing functional groups in the graphene oxide to the number of carbon atoms in the graphene oxide is (1-30): 100, respectively; the average value of the graphene oxide sheet diameter is 3-7 mu m, and the average number of layers is less than or equal to 10.
Itaconic acid is analytically pure itaconic acid.
The polymerization initiator is a free radical initiator; the adopted free radical initiator is any one of azobisisobutyronitrile, azobisisoheptonitrile, dibenzoyl peroxide and tert-butyl hydroperoxide.
The solvent is any one of dimethyl sulfoxide, dimethylformamide, dimethylacetamide and cyclobuterol.
The ultrasonic-assisted in-situ polymerization is to ultrasonically treat mixed liquid containing graphene oxide, itaconic acid, acrylonitrile, a solvent and a polymerization initiator for 1-2 hours at room temperature, then heat the mixed liquid to 40-70 ℃ for reaction for 10-30 hours, and perform ultrasonic enhancement on uniform dispersion of the graphene oxide in a polymerization system in the first 1-5 hours of the reaction.
And 2, demonomerizing and defoaming the composite spinning solution obtained in the step 1, and then preparing the composite protofilament through a spinning process.
The processes and parameters adopted by demonomerization, defoaming and spinning are all the prior art choices in the field.
And 3, carrying out pre-oxidation treatment on the composite protofilament obtained in the step 2, and then carrying out carbonization treatment in a protective atmosphere to obtain the graphene-carbon composite fiber.
The pre-oxidation treatment is carried out in the air by adopting a gradient temperature raising method, the initial temperature of the pre-oxidation treatment is 80-230 ℃, the final temperature of the pre-oxidation treatment is 260-300 ℃, the pre-oxidation treatment is carried out on the composite protofilaments in 2-6 temperature zones, and the total time of the pre-oxidation treatment is 25-100 minutes.
The carbonization treatment comprises a low-temperature carbonization part and a high-temperature carbonization part, wherein high-purity nitrogen is used as a protective gas for both the low-temperature carbonization and the high-temperature carbonization, the low-temperature carbonization temperature is 350-1000 ℃, the retention time is 1-10 minutes, and then the high-temperature carbonization is carried out, the temperature is 1100-1500 ℃, and the retention time is 0.5-5 minutes.
The embodiment also provides the graphene-itaconic acid monomer for the PAN polymer as the precursor of the carbon fiber prepared by the method, and the graphene-carbon composite fiber prepared by the graphene-itaconic acid monomer.
The invention provides a graphene-carbon composite fiber prepared from a graphene-itaconic acid monomer and a preparation method thereof. The graphene-carbon composite fiber obtained by the method has excellent mechanical properties, and solves the problems of dispersion of graphene in the fiber and chemical bonding with a carbon network structure in the fiber, so that the graphene has an obvious reinforcing effect on carbon fibers.
While the present invention has been described in detail with reference to the preferred embodiments, it should be understood that the above description should not be taken as limiting the invention. Various modifications and alterations to this invention will become apparent to those skilled in the art upon reading the foregoing description. Accordingly, the scope of the invention should be determined from the following claims.
Claims (10)
1. A method for preparing a graphene-carbon composite fiber from a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer, the method comprising:
step 1, mixing graphene oxide, an acrylonitrile monomer, an itaconic acid monomer, a solvent and a polymerization initiator to perform ultrasonic-assisted in-situ polymerization, and preparing a graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer to obtain a composite spinning solution;
step 2, the composite spinning solution obtained in the step 1 is demonomerized and defoamed, and then is spun into composite protofilaments;
and 3, carrying out pre-oxidation treatment on the composite protofilament obtained in the step 2, and then carrying out carbonization treatment in a protective atmosphere to obtain the graphene-carbon composite fiber.
2. The method for preparing the graphene-carbon composite fiber from the graphene-itaconic acid monomer for the PAN polymer of the carbon fiber precursor according to claim 1, wherein in the step 1, the mass ratio of the graphene oxide, the itaconic acid, the acrylonitrile monomer, the polymerization initiator and the solvent is (0.1-15): (1-12): (15-25): (0.15-0.75): 100.
3. the method for preparing the graphene-carbon composite fiber from the graphene-itaconic acid monomer for the PAN polymer of the carbon fiber precursor according to claim 2, wherein the ratio of the number of oxygen-containing functional groups in the graphene oxide to the number of carbon atoms of the graphene oxide is (1-30): 100, respectively; the average value of the graphene oxide sheet diameter is 3-7 mu m, and the average number of layers is less than or equal to 10.
4. The method for preparing graphene-carbon composite fibers from graphene-itaconic acid monomers for a carbon fiber precursor PAN polymer of claim 2, wherein the itaconic acid is analytically pure itaconic acid.
5. The method for preparing graphene-carbon composite fiber from graphene-itaconic acid monomer for carbon fiber precursor PAN polymer according to claim 2, wherein the polymerization initiator is a radical initiator; the adopted free radical initiator is any one of azobisisobutyronitrile, azobisisoheptonitrile, dibenzoyl peroxide and tert-butyl hydroperoxide.
6. The method for preparing graphene-carbon composite fiber from graphene-itaconic acid monomer for carbon fiber precursor PAN polymer according to claim 1, wherein the solvent is any one of dimethyl sulfoxide, dimethylformamide, dimethylacetamide and cyclobutinol.
7. The method for preparing graphene-carbon composite fibers from graphene-itaconic acid monomers for a carbon fiber precursor PAN polymer according to claim 1, wherein the ultrasonic-assisted in-situ polymerization in step 1 is that a mixed solution containing graphene oxide, itaconic acid, acrylonitrile, a solvent and a polymerization initiator is subjected to ultrasonic treatment at room temperature for 1-2 hours, then the temperature is raised to 40-70 ℃ for reaction for 10-30 hours, and the uniform dispersion of graphene oxide is ultrasonically enhanced in a polymerization system during the first 1-5 hours of the reaction.
8. The method for preparing the graphene-carbon composite fiber from the graphene-itaconic acid monomer for the PAN polymer serving as the carbon fiber precursor according to claim 1, wherein the pre-oxidation treatment in the step 3 is performed in air by a gradient temperature rise method, the initial temperature of the pre-oxidation treatment is 80-230 ℃, the final temperature of the pre-oxidation treatment is 260-300 ℃, and the pre-oxidation treatment is performed on the composite precursor in 2-6 temperature zones, wherein the total time of the pre-oxidation treatment is 25-100 minutes.
9. The method for preparing the graphene-carbon composite fiber from the graphene-itaconic acid monomer for the PAN polymer serving as the precursor of the carbon fiber according to claim 1, wherein the carbonization treatment in the step 3 comprises two parts of low-temperature carbonization and high-temperature carbonization, wherein high-purity nitrogen is used as a shielding gas in both the low-temperature carbonization and the high-temperature carbonization, the low-temperature carbonization temperature is 350-1000 ℃, the retention time is 1-10 minutes, and then the high-temperature carbonization is performed, the temperature is 1100-1500 ℃, and the retention time is 0.5-5 minutes.
10. A graphene-itaconic acid monomer for a carbon fiber precursor PAN polymer prepared in the method of any one of claims 1 to 9, and a graphene-carbon composite fiber prepared therefrom.
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| CN102560746A (en) * | 2011-12-29 | 2012-07-11 | 中国科学院宁波材料技术与工程研究所 | Preparation method of polyacrylonitrile/graphene composite-based carbon fiber |
| CN107475818A (en) * | 2017-08-18 | 2017-12-15 | 北京化工大学 | Compound carbon fiber of graphene polyacrylonitrile-radical and preparation method thereof |
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| CN102534870A (en) * | 2011-12-29 | 2012-07-04 | 中国科学院宁波材料技术与工程研究所 | Preparation method of grapheme-modified acrylonitrile base carbon fiber |
| CN102560746A (en) * | 2011-12-29 | 2012-07-11 | 中国科学院宁波材料技术与工程研究所 | Preparation method of polyacrylonitrile/graphene composite-based carbon fiber |
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