US20170327973A1 - Carbon-Fiber Precursor Fiber, Carbon Fiber, and Method for Producing Carbon Fiber - Google Patents
Carbon-Fiber Precursor Fiber, Carbon Fiber, and Method for Producing Carbon Fiber Download PDFInfo
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- US20170327973A1 US20170327973A1 US15/532,388 US201515532388A US2017327973A1 US 20170327973 A1 US20170327973 A1 US 20170327973A1 US 201515532388 A US201515532388 A US 201515532388A US 2017327973 A1 US2017327973 A1 US 2017327973A1
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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
- D01F9/24—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D01F9/28—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds from polyamides
- D01F9/30—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds from polyamides from aromatic polyamides
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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
- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/74—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polycondensates of cyclic compounds, e.g. polyimides, polybenzimidazoles
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
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- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01D—MECHANICAL METHODS OR APPARATUS IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS
- D01D10/00—Physical treatment of artificial filaments or the like during manufacture, i.e. during a continuous production process before the filaments have been collected
- D01D10/02—Heat treatment
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- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/58—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products
- D01F6/60—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides
- D01F6/605—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from homopolycondensation products from polyamides from aromatic polyamides
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- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
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- D01F6/00—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
- D01F6/88—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
- D01F6/94—Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of other polycondensation products
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- D01F9/00—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments
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- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
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- 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
- D01F9/24—Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
Definitions
- the present invention relates to: a carbon fiber precursor fiber using a novel heat-resistant aromatic polymer and not needing an infusibilization treatment (a pre-treatment including a flame resistance-imparting treatment); a carbon fiber; and a method for producing a carbon fiber.
- PAN fibers and pitch fibers are fused in the course of a carbonization treatment (a high-temperature thermal treatment at 1,000° C. or higher) and cannot maintain their fiber shapes, they are changed to infusible, flame-resistant fibers by an air oxidization treatment called an infusibilization treatment and then are subjected to carbonization to obtain carbon fibers.
- a carbonization treatment a high-temperature thermal treatment at 1,000° C. or higher
- an air oxidization treatment called an air oxidization treatment
- carbonization to obtain carbon fibers.
- some kinds of heat-resistant aromatic polymers e.g., aramid fibers and phenol resin fibers
- aramid fibers and phenol resin fibers have such properties that they are carbonized without being fused, and thus it is possible to obtain carbon fibers only by forming such polymers into fibers and subjecting the resultant fibers to a high-temperature thermal treatment.
- aramid fibers and phenol resin fibers are carbonized while maintaining their fiber shape, they have problems that their mechanical strengths (e.g., tensile strength and elastic modulus) are poor.
- the present inventors previously found out a graphite film containing a heterocyclic polymer obtained through condensation between an aromatic tetracarboxylic acid and an aromatic tetraamine (see PTL 1).
- the PBB has not yet been a widely used material and is an expensive material as compared with the existing precursor fibers.
- the PBB has not yet been a widely used material and is an expensive material as compared with the existing precursor fibers.
- a resin formed from a polymer material having a polyoxadine structure as a repeating unit is known as a relatively low cost resin (see NPL 2). That is, this polymer material is a polymer that can be synthesized using, as raw materials, phenols, anilines, and paraformaldehyde, which are widely used as organic compound materials, and thus it can be produced at a low cost.
- PTL 1 Japanese Patent Application Laid-Open (JP-A) No. 2011-57474
- NPL 2 T. Takeichi et al, Polymer 46 (2005), 12172-12180.
- an object of the present invention is to provide: a carbon fiber precursor fiber that can efficiently produce a carbon fiber at a low cost which is excellent in mechanical strengths even without an infusibilization treatment; a carbon fiber; and a method for producing the carbon fiber.
- a carbon fiber precursor fiber including:
- X and Y each independently represent a divalent substituent, a single bond, or a structure forming a fused ring by sharing one side of two adjacent rings, and the divalent substituent is selected from the group consisting of —O—, —S—, —OSO—, —NH—, —CO—, —CH 2 —, and —CH(CH 3 ) 2 —.
- ⁇ 3> A carbon fiber obtained by carbonizing the carbon fiber precursor fiber according to ⁇ 1> or ⁇ 2> above.
- a method for producing a carbon fiber including:
- X and Y each independently represent a divalent substituent, a single bond, or a structure forming a fused ring by sharing one side of two adjacent rings, and the divalent substituent is selected from the group consisting of —O—, —S—, —OSO—, —NH—, —CO—, —CH 2 —, and —CH(CH 3 ) 2 —.
- Ar 1 represents an aryl group expressed by any one of Structural Formulas (1) to (5) below
- Ar 2 represents an aryl group expressed by Structural Formula (6) or (7) below:
- the present invention it is possible to solve the above existing problems and provide a carbon fiber precursor fiber that can efficiently produce a carbon fiber at a low cost which is excellent in mechanical strengths even without an infusibilization treatment; a carbon fiber; and a method for producing the carbon fiber.
- FIG. 1A is a scanning microscopic image of carbon fibers according to Example 1-2.
- FIG. 1B is a scanning microscopic image that is enlarged in the fiber length direction of the carbon fibers depicted in FIG. 1A .
- FIG. 1C is a scanning microscopic image that is enlarged in the fiber diameter direction of the carbon fibers depicted in FIG. 1A .
- FIG. 2A is a conceptual diagram indicating plane interval c/2 of carbon network planes and stack thickness Lc of carbon network planes in a graphite crystal.
- FIG. 2B is a conceptual diagram indicating an optical system in measuring wide angle X-ray diffraction.
- a carbon fiber precursor fiber of the present invention is a fibrous material containing a polymer containing a constituent unit represented by General Formula (1) below.
- the fibrous material of the polymer can be carbonized as is without an infusibilization treatment. Also, it can have sufficient mechanical strengths when carbonized with a thermal treatment.
- One possible reason for this is as follows. Specifically, as represented in the General Formula (1), the polymer has a rod-like aromatic polymer structure at the stage before formed into a fiber. With this structure, the polymer has such a property that the molecules will easily be arranged in the fiber axis direction by the action of stress which the polymer chains will receive upon spinning. Once such a property has been imparted thereto upon the spinning, development of graphite crystals is made possible upon the carbonization while maintaining the fiber axis orientability.
- the cross-linked structure between the polymer chains through ring-opening polymerization unique to an oxazine ring makes it possible to allow the carbon fiber tissue structure to have an appropriate level of a non-crystalline structure which is necessary for increasing the strength of carbon fibers.
- X and Y each independently represent a divalent substituent, a single bond, or a structure forming a fused ring by sharing one side of two adjacent rings, and the divalent substituent is selected from the group consisting of —O—, —S—, —OSO—, —NH—, —CO—, —CH 2 —, and —CH(CH 3 ) 2 —.
- the polymer containing the constituent unit represented by the General Formula (1) can be synthesized by the following method.
- the above polymer can be obtained through reaction between the following starting materials: an aromatic dihydroxy compound represented by General Formula (3) below or a derivative of the aromatic dihydroxy compound such is as an acid chloride thereof, an acid anhydride thereof, an ester thereof, or an amide thereof; an aromatic diamine represented by General Formula (4) below or a salt thereof; and paraformaldehyde.
- an aromatic dihydroxy compound represented by General Formula (3) below or a derivative of the aromatic dihydroxy compound such is as an acid chloride thereof, an acid anhydride thereof, an ester thereof, or an amide thereof
- an aromatic diamine represented by General Formula (4) below or a salt thereof such as an acid chloride thereof, an acid anhydride thereof, an ester thereof, or an amide thereof
- paraformaldehyde an aromatic dihydroxy compound represented by General Formula (3) below or a derivative of the aromatic dihydroxy compound such is as an acid chloride thereof, an acid anhydride thereof, an ester thereof, or an amide thereof
- X and Y each independently represent a divalent substituent, a single bond, or a structure forming a fused ring by sharing one side of two adjacent rings, and the divalent substituent is selected from the group consisting of —O—, —S—, —OSO—, —NH—, —CO—, —CH 2 —, and —CH(CH 3 ) 2 —.
- aromatic dihydroxy compound examples include 4,4-dihydroxydiphenyl ether, bis(4-hydroxyphenyl)methane, bis(4-hydroxyphenyl)sulfide, bis(4-hydroxyphenyl)sulfone, bis(4-hydroxyphenyl)amine, 4′4-dihydroxybenzophenone, and 2,2,-bis(4-hydroxyphenyl)propane.
- aromatic diamine compound examples include 4,4-diaminodiphenyl ether (which is also called 4,4-oxydianiline), bis(4-aminophenyl)sulfide, bis(4-aminophenyl)sulfone, bis(4-aminophenyl)amine, 4′4-diaminobenzophenone, and 2,2,-bis(4-aminophenyl)propane.
- 4,4-diaminodiphenyl ether which is also called 4,4-oxydianiline
- bis(4-aminophenyl)sulfide bis(4-aminophenyl)sulfone
- bis(4-aminophenyl)amine bis(4-aminophenyl)amine
- 4′4-diaminobenzophenone bis(4-aminophenyl)amine
- 2,2,-bis(4-aminophenyl)propane 2,2,-bis(4-aminopheny
- Examples of the structure forming a fused ring by sharing one side of two adjacent rings in X or Y in the General Formula (3) or (4) include a structure where the two adjacent rings form a naphthalene ring.
- the structures of X and Y are introduced into the constituent unit represented by the General Formula (1) as the structures of X and Y in the General Formula (1).
- a polymerizing method for obtaining the polymer is, for example, as follows. Specifically, the aromatic dihydroxy compound or the derivative thereof and the aromatic diamine or the salt thereof are added to a reaction vessel containing the paraformaldehyde and a solvent. In chloroform, the resultant mixture is stirred and refluxed for 3 hours to 48 hours, to obtain the polymer containing the constituent unit represented by the General Formula (1).
- the solvent is not particularly limited so long as it is a solvent that can dissolve the starting materials and does not prevent the polymerization.
- Specific examples of the solvent include chloroform, methanol, benzene, and toluene.
- These compounds used as starting materials for the synthesis of the polymer may be synthesized by known methods or may be commercially available products that are purchased.
- the carbon fiber precursor may be a fibrous material obtained from the polymer itself containing the constituent unit represented by the General Formula (1) as a repeating unit, but so long as the effects of the present invention are not impeded, the carbon fiber precursor may also be a fibrous material obtained from the above polymer having the end to which any substituent has been added.
- substituents examples include an ester group, an amide group, an imide group, a hydroxyl group, and a nitro group.
- the number of the repeating units of the constituent unit represented by the General Formula (1) is about 100 to about 100,000.
- the carbon fiber precursor fiber can be produced by spinning a compound to be spun (polymer) containing the polymer containing the constituent unit represented by the General Formula (1).
- An intrinsic viscosity of the compound to be spun is not particularly limited but is preferably 0.05 dL ⁇ g ⁇ 1 to 5 dL ⁇ g ⁇ 1 .
- the fibers When the intrinsic viscosity thereof is less than 0.05 dL ⁇ g ⁇ 1 , the fibers may be fractured during spinning. When it is more than 5 dL ⁇ g ⁇ 1 , the compound to be spun may not homogeneously dissolve in the below-described solvent used for spinning. Note that, 1 dL ⁇ g ⁇ 1 is equivalent to 10 ⁇ 4 m 3 ⁇ g ⁇ 1 .
- the carbon fiber precursor fiber may be a fibrous material obtained from a copolymer obtained by copolymerizing the constituent unit represented by the General Formula (1) and another constituent unit.
- the carbon fiber precursor fiber may also be a fibrous material containing another polymer.
- Such another polymer is not particularly limited so long as it is a polymer that can be carbonized even without an infusibilization treatment.
- examples thereof include aromatic polyamide, polyimide, polyoxadiazole, polyimidazole, and other polymers.
- the polymer containing the constituent unit represented by the General Formula (2) is preferable from the viewpoint of increasing the mechanical strengths.
- Ar 1 represents an aryl group expressed by any one of Structural Formulas (1) to (5) below
- Ar 2 represents an aryl group expressed by Structural Formula (6) or (7) below.
- the polymer containing the constituent unit represented by the General Formula (2) can be synthesized by the following method.
- aromatic tetracarboxylic acid or aromatic tetracarboxylic acid derivatives such as acid chlorides, acid anhydrides, esters or amides thereof, with aromatic tetraamine or salts thereof.
- aromatic tetracarboxylic acids examples include 1,4,5,8-naphthalenetetracarboxylic acid and 4,4′-binaphthy-1,1′,8,8′-tetracarboxylic acid.
- aromatic tetraamines examples include 1,2,4,5-benzenetetraamine and 3,3′,4,4′-biphenyltetraamine.
- the aromatic tetracarboxylic acid or carboxylic acid derivatives thereof and the aromatic tetraamine or salts thereof are added to a reaction vessel containing a solvent, and the mixture is stirred at 100° C. to 250° C. for 3 hours to 48 hours, to thereby obtain the polymer containing the constituent unit represented by the General Formula (2) as a repeating unit.
- the solvent is not particularly limited so long as it can dissolve the starting materials and formed polymers and has an effect as a catalyst of promoting polymerization.
- Specific examples thereof include polyphosphoric acid, polyphosphoric acid esters, and cresyl diphenyl phosphate, as well as methane sulfonic acid in which diphosphorus pentoxide or the like has been dissolved.
- the 1,4,5,8-naphthalenetetracarboxylic acid can be synthesized from pyrene in 2 steps consisting of oxidation with potassium permanganate and oxidation with sodium hypochlorite solution.
- the 4,4′-binaphthy-1,1′,8,8′-tetracarboxylic acid can be synthesized from 4-chloro-1,8,-naphthalic anhydride in 3 steps consisting of esterification, coupling, and hydrolysis.
- the 1,2,4,5-benzenetetraamine can be synthesized from m-chlorobenzene in 3 steps consisting of nitration, amination, and reduction of the nitro group, and isolated and used as tetrahydrochloride thereof.
- the 3,3′,4,4′-biphenyltetraamine can be synthesized from o(ortho)-nitroaniline in 3 steps consisting of iodination, cross coupling, and reduction of the amino group.
- the polymer represented by the General Formula (2) may have any substituent added to the end thereof.
- substituents examples include an ester group, an amide group, an imide group, a hydroxyl group, and a nitro group.
- the number of the repeating units of the constituent unit represented by the General Formula (2) is about 100 to about 100,000.
- a mixing ratio of the polymer containing the constituent unit represented by the General Formula (1) and the polymer containing the constituent unit represented by the General Formula (2) is preferably 1/3 to 3 as a mass ratio expressed by the following formula; i.e., “the polymer containing the constituent unit represented by the General Formula (2)/the polymer containing the constituent unit represented by the General Formula (1)”.
- the carbon fiber precursor fiber can be produced by spinning compounds to be spun including the polymer containing the constituent unit represented by the General Formula (1) and if necessary, the polymer containing the constituent unit represented by the General Formula (2) and the like.
- a method for the spinning is not particularly limited and may be appropriately selected depending on the intended purpose. Examples thereof include known wet-type spinning methods and dry-type spinning methods.
- a solvent used in the wet-type spinning methods and dry-type spinning methods is not particularly limited so long as it is a solvent in which the compound to be spun can dissolve.
- examples thereof include chloroform, toluene, and methanesuofonic acid.
- a coagulation liquid for eluting the solvent and coagulating the compound to be spun as the carbon fiber precursor fiber is not particularly limited. Examples thereof include water, alcohol, and diluted sulfuric acid.
- the carbon fiber precursor fiber is made large in its fiber diameter, the carbon fiber precursor fiber is not impaired in its shape upon the subsequent carbonization treatment.
- the fiber diameter thereof is not particularly limited and may be appropriately selected depending on the intended purpose. It may be 50 ⁇ m or more, if necessary. Note that, the upper limit of the fiber diameter is about 1,000 ⁇ m.
- a drawing treatment may be performed, if necessary.
- spun yarn may be drawn directly in a coagulation bath, or wound yarn may be washed with water and then drawn in the bath.
- a draw ratio is preferably about 1.2 times to about 10 times.
- a carbon fiber of the present invention can be obtained by carbonizing the carbon fiber precursor fiber. Also, a method for producing the carbon fiber includes a carbonization step of heating the carbon fiber precursor fiber under inert gas to carbonize the carbon fiber precursor fiber.
- the inert gas is not particularly limited, and examples thereof include nitrogen and argon gas.
- a method for the heating is, for example, a method of performing pre-heating for ring-opening polymerization of the oxazine ring of the polymer containing the constituent unit represented by the General Formula (1) and then post-heating for carbonization of the ring-opening polymer.
- the pre-heating is not particularly limited so long as the ring-opening polymerization reaction can proceed. However, it is preferably performed under temperature conditions of 200° C. to 600° C. in a nitrogen atmosphere for the purpose of making the production process highly efficient. When the drawing treatment is performed, this pre-heating may be performed at the same time as the drawing treatment.
- the post-heating in the carbonization step can be rapidly performed.
- a temperature increasing rate can be set to 5° C./min or more.
- the upper limit of the temperature increasing rate is about 500° C./min.
- the temperature conditions of the post-heating heated most are preferably 800° C. to 2,000° C. Heating at such a temperature makes it possible to carbonize the carbon fiber precursor fiber while maintaining its shape.
- the carbon fiber precursor fiber containing the polymer containing the constituent unit represented by the General Formula (1) it is possible to moderately perform both development of graphite crystals and impartment of a three-dimensional crosslinked structure, which makes it possible to produce carbon fibers having sufficient mechanical properties.
- the method for producing the carbon fiber may include, after the carbonization step or successively with the carbonization step, a graphitizing step of heating the carbon fiber at a higher temperature to graphitize the carbon fiber.
- the graphitizing step is preferably performed under the inert gas similar to the carbonization step.
- the method for producing the carbon fiber may further include steps of performing a surface treatment and a sizing impartment, which are performed in known carbon fiber production processes.
- the carbon fibers By spinning the carbon fiber precursor fibers so as to be thick fibers in the spinning, the carbon fibers can be increased in diameter while maintaining mechanical strengths.
- Commercially available carbon fibers such as PAN-type carbon fibers usually have a fiber diameter of about 7 ⁇ m. Mechanical strengths of the carbon fibers are maintained not only in the case where the fiber diameter is 1 ⁇ m or more but less than 8 ⁇ m, but also in the case where the fiber diameter is 8 ⁇ m or more, and even in the case where the fiber diameter is 16 ⁇ m or more. Note that, the upper limit of the fiber diameter is about 30 ⁇ m.
- the carbon fibers can be formed into short fibers (spun) or continuous fibers (filament).
- polyBPF/ODA oxazine poly(N,N′-oxydiphenylene-4,4′-methylene dibenzoxazine)
- BNTCA 4,4′-binaphthy-1,1′,8,8′-tetracarboxylic acid
- DMAc in the Synthesis Scheme (2) means dimethyl acetoamide.
- FIGS. 1A to 1C Microscopic images of the obtained carbon fibers according to Example 1-2 are depicted in FIGS. 1A to 1C .
- FIG. 1A is a scanning microscopic image of the carbon fibers according to Example 1-2.
- FIG. 1A is a scanning microscopic image of the carbon fibers according to Example 1-2.
- FIG. 1A is a scanning microscopic image of the carbon fibers according to Example 1-2.
- Carbon fibers according to Comparative Example 1-1 were produced in the same manner as in Example 1-1 except that the composition of the raw liquid for spinning was changed; i.e., the raw liquid for spinning used was prepared by dissolving only 50 g of PBB in 1 L of the methanesulfonic acid, and that the heat treatment at 240° C. for 30 minutes was not performed and the carbonization was performed by heating from room temperature to 1,300° C. at a temperature increasing rate of 10° C./min and maintaining for 10 minutes. The obtained carbon fibers were found to have a fiber diameter of about 9 ⁇ m.
- Carbon fibers according to Comparative Example 1-2 were produced in the same manner as in Comparative Example 1-1 except that the carbonization temperature was changed, i.e., the carbon fiber precursor fibers were carbonized by being heated from room temperature to 1,500° C. at a temperature increasing rate of 10° C./min in a nitrogen atmosphere and maintained for 10 minutes.
- the obtained carbon fibers were found to have a fiber diameter of about 9 ⁇ m.
- Table 1 below presents densities of the carbon fibers calculated by the sink-float method.
- the carbon fibers according to Examples 1-1 to 3-2 have slightly low or almost equivalent densities as compared with the carbon fibers according to Comparative Examples 1-1 and 1-2.
- the densities of the carbon fibers according to Examples 1-1 to 3-2 are almost equivalent to the densities of commercially available PAN-type carbon fibers which are about 1.76 to about 1.81. Therefore, the carbon fibers according to Examples 1-1 to 3-2 can be produced to have equivalent densities to those of the practical products.
- the carbon fibers according to Examples 1-1 to 3-2 can be made thicker to have a diameter of 9 ⁇ m or 16 ⁇ m, as compared with the diameters of commercially available carbon fibers which are 5 ⁇ m to 7 ⁇ m.
- FIG. 2A is a conceptual diagram indicating plane interval c/2 of carbon network planes and stack thickness L c of carbon network planes in a graphite crystal. Note that, reference signs 1 a, 1 b and 1 c in FIG. 2A denote carbon network planes.
- the measurement of the plane interval c/2 of carbon network planes and the stack thickness L c of carbon network planes was performed by measuring a wide angle X-ray diffraction profile with an X-ray diffraction device using CuK ⁇ rays monochromatized with a Ni filter as an X-ray source. Specifically, in the optical system for an equatorial direction illustrated in FIG. 2B , the plane interval c/2 of carbon network planes and the stack thickness L c of carbon network planes were obtained from the peak of plane index (002) observed at 29 of about 26° in the equatorial direction profile. Note that, FIG.
- orientation degree f of the graphite crystals obtained from the above-described azimuth measurement is used as an index of a carbon fiber having practical strength and elastic modulus.
- Table 2 below presents the plane interval c/2 of the carbon network planes, the stack thickness L c of the carbon network planes, and the orientation degrees (f) of the graphite crystals in the carbon fibers according to Examples 1-2, 2-2, and 3-2 and the carbon fibers according to Comparative Example 1-2, which were carbonized at the carbonization temperature of 1,500° C., and the PAN-type carbon fibers and the pitch-type carbon fibers.
- “*” means that the indicated values are the numerical values disclosed in Referential Document 1.
- the values of the plane interval c/2 of the carbon network planes, the stack thickness L c of the carbon network planes, and the orientation degrees f of the carbon fibers according to Examples 1-2, 2-2, and 3-2 are equivalent to those of the carbon fibers according to Comparative Example 1-2 derived from PBB, indicating that the carbon fibers excellent in mechanical strengths can be produced at a lower cost.
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Cited By (4)
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US11306229B2 (en) | 2016-10-26 | 2022-04-19 | Compagnie Generale Des Etablissements Michelin | Polybenzoxazine that can be used for coating metal and for the bonding of same to rubber |
US11370935B2 (en) | 2016-10-26 | 2022-06-28 | Compagnie Generale Des Etablissements Michelin | Metal or metallized reinforcement with polybenzoxazine-coated surface |
US11624002B2 (en) | 2017-06-14 | 2023-04-11 | Compagnie Generale Des Etablissements Michelin | Sulfurized polybenzoxazine that can be used for coating metal and for the bonding of same to rubber |
US11701922B2 (en) | 2017-06-14 | 2023-07-18 | Compagnie Generale Des Etablissements Michelin | Metal or metal-plated reinforcement with sulfur polybenzoxazine-coated surface |
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CN112481817A (zh) * | 2020-11-27 | 2021-03-12 | 中宝(西安)科技集团有限公司 | 一种碳纤维隔热材料及其制备方法 |
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US3666417A (en) * | 1969-05-17 | 1972-05-30 | Kureha Chemical Ind Co Ltd | Process for production of carbon fibers |
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JPS4954629A (zh) * | 1972-09-21 | 1974-05-28 | ||
US5152939A (en) * | 1991-03-12 | 1992-10-06 | Edison Polymer Innovation Corp. | Composite densification with benzoxazines |
JP2003064180A (ja) * | 2001-06-11 | 2003-03-05 | Nippon Steel Chem Co Ltd | ジヒドロベンゾキサジン環構造を有する硬化性樹脂及び耐熱性硬化樹脂 |
JP2006144201A (ja) * | 2004-11-24 | 2006-06-08 | Seiko Epson Corp | 炭素複合体、炭素複合体の製造方法および樹脂成形体 |
TW200801077A (en) * | 2006-05-01 | 2008-01-01 | Sekisui Chemical Co Ltd | Sintered resin product and electronic device comprising the same |
US20110269857A1 (en) * | 2008-10-09 | 2011-11-03 | Industry-University Cooperation Foundation, Hanyang University | Polymer and method of preparing the same |
EP2927351B1 (en) * | 2012-11-27 | 2024-02-21 | National Institute of Advanced Industrial Science and Technology | Precursor fiber for carbon fibers, and method for producing carbon fiber |
EP3141637B1 (en) * | 2014-05-08 | 2019-04-03 | National Institute of Advanced Industrial Science and Technology | Polybenzimidazole carbon fiber and method for manufacturing same |
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US3666417A (en) * | 1969-05-17 | 1972-05-30 | Kureha Chemical Ind Co Ltd | Process for production of carbon fibers |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11306229B2 (en) | 2016-10-26 | 2022-04-19 | Compagnie Generale Des Etablissements Michelin | Polybenzoxazine that can be used for coating metal and for the bonding of same to rubber |
US11370935B2 (en) | 2016-10-26 | 2022-06-28 | Compagnie Generale Des Etablissements Michelin | Metal or metallized reinforcement with polybenzoxazine-coated surface |
US11624002B2 (en) | 2017-06-14 | 2023-04-11 | Compagnie Generale Des Etablissements Michelin | Sulfurized polybenzoxazine that can be used for coating metal and for the bonding of same to rubber |
US11701922B2 (en) | 2017-06-14 | 2023-07-18 | Compagnie Generale Des Etablissements Michelin | Metal or metal-plated reinforcement with sulfur polybenzoxazine-coated surface |
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US20200378036A1 (en) | 2020-12-03 |
EP3228736B1 (en) | 2022-01-26 |
CN107002300A (zh) | 2017-08-01 |
WO2016088663A1 (ja) | 2016-06-09 |
JPWO2016088663A1 (ja) | 2017-09-14 |
JP6590283B2 (ja) | 2019-10-16 |
EP3228736A1 (en) | 2017-10-11 |
KR20170088968A (ko) | 2017-08-02 |
KR101933598B1 (ko) | 2018-12-28 |
EP3228736A4 (en) | 2018-06-27 |
CN107002300B (zh) | 2019-09-17 |
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