JPH1025625A - Carbon fiber and carbon fiber assembly - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide carbon fiber having high electrical resistance and high strength required for an antistatic material for electronic parts and a wave- absorbing material for outer wall materials. SOLUTION: This carbon filament fiber has a volume resistivity value of 10<-2> -10<2> Ω.cm, a carbon content of 85-95wt.%, a hydrogen content of 0.3-2.5wt.%, the graphic lattice constant(Lc) of <=25Å and the spacing d002 of >=3.45Å according to X-ray diffraction.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

BACKGROUND OF THE INVENTION The present invention relates to 10 ^-2 to 10 ² Ω.
TECHNICAL FIELD The present invention relates to a carbon fiber having a high volume specific electric resistance of 1 cm and a carbon fiber aggregate using the same.

[0002]

2. Description of the Related Art Carbon fibers are classified into polyacrylonitrile (PAN) -based carbon fibers, pitch-based carbon fibers, and the like according to their raw materials. Among them, pitch-based carbon fibers are roughly classified into high-performance carbon fibers and general-purpose carbon fibers according to the method of preparing the raw materials. High-performance carbon fiber is made from pitch obtained from coal, petroleum, etc., which is heated and used to generate an optically anisotropic portion of the liquid crystal which is the precursor of the carbon structure. Spinning, infusibilizing under an oxidizing atmosphere, carbonizing,
It is obtained by performing graphitization as needed. Here, the reason for causing the optical anisotropy is that the carbon fiber obtained because the optically anisotropic portion having liquid crystallinity has good orientation also has excellent orientation, and has high strength and high strength. This is because the elastic modulus is easily developed.

In recent years, materials having a high electric resistance have been required as antistatic materials for electronic components and the like and radio wave absorbing materials such as outer wall materials. Development is desired.

[0004]

The relationship between the carbonization temperature and the electric resistance has been known in the art, and the electric resistance decreases as the carbonization temperature increases (for example, "Carbon Fiber" published by Kyundai Kogyosha). See page 83). Conventionally, if carbon fibers are manufactured at a firing temperature in a range where a desired electric resistance can be obtained, high tensile strength and tensile modulus cannot be obtained because pitch-based carbon fibers have a low firing temperature. In this case, the nitrogen is not completely removed, resulting in a fiber having a low carbon content, which is not preferable. Moreover, in the case of PAN-based carbon fibers, those having high electric resistance like pitch-based carbon fibers cannot be obtained.

[0005]

Means for Solving the Problems The present inventors have solved the above-mentioned conventional problems and made intensive studies to obtain a carbon fiber having a high electric resistance. As a result, the present inventors have reached the present invention. That is, the gist of the present invention is that the volume specific electric resistance value is 10 ⁻² to 10 ² Ωcm.
And a carbon content of 85 to 95% and a hydrogen content of 0.1%.
A carbon fiber characterized by being 3 to 2.5%, having a lattice constant Lc of graphite of not more than 25 ° determined by X-ray diffraction, having an interplanar spacing d002 of not less than 3.45 °, and being a long fiber; Carbon fiber bundle.

[0006]

BEST MODE FOR CARRYING OUT THE INVENTION The carbon fiber of the present invention has a volume specific electric resistance of 10 ⁻² to 10 ² Ω · cm, preferably 10 ^−1.
10 to 10 Ω · cm. Volume specific electric resistance value is 10 ^-2 Ω
If it is smaller than 10 cm, the electric resistance is too small, so that it is not preferable as a material for antistatic or radio wave absorption.
^If it is larger than ² Ω · cm, the carbon fiber becomes extremely unstable and fragile, which is not preferable.

The carbon fiber of the present invention has a carbon content of 85 to 85%.
95%, preferably 90-95%, and the hydrogen content is 0.3-2.5%, preferably 0.8-2.0%. If the carbon content is less than 85% and the hydrogen content is more than 2.5%, the carbon fiber becomes extremely unstable and fragile, which is not preferable. If the content is less than 0.3%, it is not preferable because a radio wave absorber having good characteristics cannot be formed.

The carbon fiber of the present invention has a lattice constant Lc of graphite of 25 ° or less, preferably 10 to 10%, determined by X-ray diffraction.
20 °, and the plane interval d002 is 3.45 ° or more, preferably 3.45 to 3.48 °. If Lc is larger than 25 ° and d002 is smaller than 3.445 °, it is not preferable because a radio wave absorber having good characteristics cannot be formed.

Next, the manufacturing method of the present invention will be described. As the raw material pitch used in the present invention, for example,
Carbonaceous raw materials such as coal-based coal tar, coal tar pitch, coal liquefaction, petroleum-based heavy oil, pitch, petroleum resin and its thermal polycondensation reaction products, and polymerization reaction products by the catalytic reaction of naphthalene and anthracene Is mentioned. Also,
These carbonaceous raw materials may be used after being subjected to a preliminary treatment such as a heating treatment followed by extraction of a soluble component with a solvent or a hydrogenation treatment in the presence of a hydrogen-donating solvent or hydrogen gas.

The raw material pitch contains ash (Ash component) as an insoluble substance. This is due to an optically anisotropic material which becomes a precursor of carbon fiber by heating the raw material pitch. In the case of the liquid crystal pitch, it causes non-uniformity and gives a precursor of disordered structure. Further, after spinning, the fiber obtained by infusibilizing and firing produces physical defects, which adversely affects strength and elastic modulus.

[0011] Therefore, if a pitch having an ash content of usually 30 ppm or less, preferably 20 ppm or less is used in the stage of spinning, carbon fibers having high tensile strength can be obtained, and the carbon fiber bundle also serves as a reinforcing material. This is useful when used. The ash may be removed at any time before spinning, for example, at the raw material pitch stage or the spinning pitch stage. The ash may be removed by a known method. For example, there are a sedimentation method, a centrifugal separation method, a filtration method, an adsorption method, an acid, an alkali, a washing method with a solvent, and the like. May be repeated. It is also effective to add a porous inorganic substance (such as a filter aid) to increase the efficiency of removal. Industrially, it is preferable to use a sedimentation method, a centrifugal separation method, or a filtration method since continuous or large-scale treatment can be performed.

[0012] The pitch purified as described above is converted into a liquid crystal pitch having optical anisotropy according to a conventional method. The optical anisotropy ratio of the pitch used for spinning needs to be 80% or more, preferably 90% or more, and more preferably 95% or more. 80% optical anisotropy
If it is less than, the strength of the carbon fiber is remarkably reduced, and if the firing temperature is increased to increase the tensile strength, the electric resistance is inevitably reduced, and a carbon fiber having a desired high electric resistance cannot be obtained.

Incidentally, the optical anisotropy ratio of the pitch is a value obtained by using a portion showing the optical anisotropy in the pitch sample under a polarizing microscope at room temperature as an area ratio. Specifically, for example, a sample obtained by crushing a pitch sample into a few mm square is embedded in a substantially whole surface of a resin having a diameter of about 2 cm according to a conventional method, and after polishing the surface, the entire surface is polarized. It is determined by observing under a microscope (100 times magnification) and measuring the area ratio of the optically anisotropic portion to the total surface area of the sample.

A method for producing an optically anisotropic liquid crystal pitch can also be a known method. For example, the refined pitch is brought to 350-500 ° C., preferably 380-45 ° C.
At 0 ° C. for 2 minutes to 50 hours, preferably for 5 minutes to 5 hours, under an atmosphere of an inert gas such as nitrogen, argon, or steam,
Alternatively, there is a method of performing heat treatment under blowing or under reduced pressure. As another example, a method of polymerizing a condensed polycyclic hydrocarbon such as naphthalene in the presence of a catalyst such as HF / BF3, or performing a solvent separation using a solvent having a specific solubility parameter on a raw material pitch, There is a method for obtaining a desired pitch.

[0015] The carbon content of the spinning pitch is at least 93%, particularly preferably at least 95%. If the carbon content is less than 93%, as in the case of the above-mentioned ash, nitrogen, sulfur, oxygen, etc., which are foreign elements, cause a reduction in strength, and lower the tensile strength of carbon fibers. Using the above-described spinning pitch, melt spinning is performed to obtain pitch fibers. The obtained pitch fiber has a low breaking strength as a single fiber.
0000 pitch fibers are bundled with a sizing agent to form a pitch fiber tow. As the sizing agent, one that dissolves a part of the pitch fibers or adheres or fuses the fibers during the infusibilization treatment is required, and for example, a water emulsion of silicone oil is preferable. Further, in order to more effectively avoid fusion, inorganic fine particles such as carbon black and SiC may be added to the sizing agent.

The pitch fiber tow is heated to 160 to 400 ° C. in an oxidizing gas atmosphere to make it infusible. The obtained infusible fiber tow is calcined in an atmosphere of an inert gas such as nitrogen or argon to obtain carbon fibers. In the present invention, first, in a state where tension is not applied to the infusible fiber tow,
The first carbonization treatment is performed at a temperature of 450 to 600C, preferably 520 to 580C. The temperature of the first carbonization treatment is 450 ° C
If it is lower, the fiber strength is not enough to withstand the tension of the second carbonization treatment, and if it is higher than 600 ° C., the elongation of the fiber decreases, and it is also possible to withstand the tension of the second carbonization treatment. It is not preferable because it cannot be done.

The basis weight of the carbonized yarn obtained by performing the first carbonization treatment is 1.6 to 6.0 g / m, preferably 1.8 to 4.5.
g / m. If the basis weight is less than 1.6 g / m, a large number of carbon fibers must be used when manufacturing a composite material having a predetermined shape. Therefore, if the basis weight is greater than 6.0 g / m, tension is applied. When the second carbonization is performed, the alignment of each fiber in the fiber axis direction is undesirably reduced.

The time for the first carbonization treatment is usually 1 second to 10 seconds.
Minutes, preferably 10 seconds to 5 minutes. Next, while applying a tension of 50 g or more, preferably 80 g or more per 1000 filaments, to the first carbonization-treated fiber tow, 700 to 1000 ° C., preferably 730 to 90 ° C.
The second carbonization treatment is performed at 0 ° C, more preferably at a temperature of 750 to 850 ° C. If the temperature of the second carbonization treatment is lower than 700 ° C., the strength and the radio wave absorption characteristics are not sufficient, and
If it exceeds 1000 ° C., only carbon fibers having low electric resistance can be obtained.

The time for the second carbonization treatment is usually 1 second to 10 seconds.
Minutes, preferably 10 seconds to 5 minutes. If the time of the second carbonization treatment is shorter than 1 second, the control of the residence time, that is, the control of the degree of carbonization becomes difficult, and the variation of the electric resistance value becomes large. It is not preferable because it becomes large. Next, a method for producing the carbon fiber aggregate of the present invention will be described.

As is well known, the long-fibrous carbon fiber tow obtained as described above is usually produced in a state where many single fibers having a diameter of several μm to several tens μm are bundled. The carbon fiber bundle to be used is prepared by combining this or a larger number of them and binding them with a binder such as resin or asphalt,
It is integrated. As a resin as a binder,
For example, epoxy resin, phenolic resin, saturated or unsaturated polyester, polyphenylene sulfide, polyphenylene ether, polycarbonate, polyoxymethylene, polystyrene, polyolefin, polyurethane resin, acrylic resin, vinyl acetate resin, homopolymer such as polyamide resin, or copolymer, etc. Is mentioned.
Of these, epoxy resins, phenol resins, water-soluble polyamide resins, and polyurethane resins are particularly preferred.

A method of applying a binder to carbon fibers can be performed by a known method. For example, 5000-4000
After impregnating the binder into 0 long fibrous carbon fiber tows,
There is a method of drying. The form of the binder at the time of impregnation may be dissolved in an appropriate solvent or dispersed in water as an emulsion using a surfactant. Examples of the solvent used include 2-butanone, tetrahydrofuran, N, N-dimethylformamide, acetone, chloroform, dichloromethane and the like.

The bonding state by the binder may be any bonding state depending on the application, from a weak bonding state in which the carbon fiber bundles maintain the integrity to a strong bonding state called a so-called carbon fiber rod. It can be. Normal,
The binder can be bound by adhering 0.2 to 10% by weight, preferably 0.5 to 7% by weight, based on the total amount of carbon fibers.

The thickness (cross-sectional area) of the carbon fiber aggregate of the present invention
Is usually 0.2 to 80 mm as the total cross-sectional area of the carbon fiber.
² , preferably 0.8 to ²⁰ mm ² . The shape is arbitrary, but a rod-like shape such as a round bar is preferable from the viewpoint of handleability and the like. However, if desired, it may be in the form of a string, a plate or the like. An arbitrary length can be selected for the length of the carbon fiber aggregate depending on the application.

The carbon fiber and the carbon fiber bundle of the present invention are:
Since it has high electric resistance and high strength, it can be suitably used as an antistatic material for electronic components and the like and a radio wave absorbing material such as an outer wall material for high-rise buildings.

[0025]

EXAMPLES The present invention will be described more specifically with reference to the following examples, but the present invention is not limited to the following examples. Example 1 A spinning pitch having an optical anisotropy of 100%, a Mettler softening point of 302 ° C., a carbon content of 96% by weight, and an ash content of 17 ppm was spun at a die temperature of 337 ° C. while being bundled with a silicon-based oil agent. 11,000 length 7000m
Was obtained.

The obtained pitch fiber tow was heated to 380 ° C. at a heating rate of 1 ° C./min in the air and heated to make it infusible. Next, in a nitrogen gas atmosphere, the first carbonization treatment was performed at 560 ° C. and a residence time of 2 minutes without applying tension to the infusibilized fiber tow. The basis weight of the carbonized yarn obtained in the first carbonization treatment was 2.1 g / m. Further, in a nitrogen gas atmosphere, a tension of 1320 g / tow (120 g / 1000 strands) was applied to the first carbonized fiber tow, and
The second carbonization treatment was performed under the conditions of ° C. and a residence time of 2.5 minutes to produce carbon fibers.

The carbon fiber obtained has a carbon content of 93%,
The hydrogen content was 1.3%, the lattice constant Lc of graphite determined by X-ray diffraction was 17 °, the spacing d002 was 3.46 °, and the volume specific electrical resistance was 0.8 Ω · cm. The obtained carbon fiber tow is solidified with epoxy resin and CF cross section is about 1.3m
An m ² string-like carbon fiber bundle was produced. Example 2 A spinning pitch having an optical anisotropy of 100%, a Mettler softening point of 302 ° C., a carbon content of 96% by weight, and an ash content of 30 ppm was spun at a die temperature of 337 ° C. while being bundled with a silicon-based oil agent. 10,000 length 7000m
Was obtained.

The pitch fiber tow thus obtained was heated to 380 ° C. at a heating rate of 1 ° C./min in the air and heated to make it infusible. Next, in a nitrogen gas atmosphere, the first carbonization treatment was performed at 530 ° C. and a residence time of 2 minutes without applying tension to the infusible fiber tow. The basis weight of the carbonized yarn obtained in the first carbonization treatment was 1.9 g / m. Further, in a nitrogen gas atmosphere, a tension of 1200 g / tow (120 g / 1000 strands) is applied to the first carbonized fiber tow, and 780 g is applied.
The second carbonization treatment was performed at a temperature of 2 ° C. and a residence time of 2 minutes to produce carbon fibers.

The carbon fiber obtained has a carbon content of 92%,
The hydrogen content was 1.5%, the lattice constant Lc of graphite determined by X-ray diffraction was 17 °, the interplanar spacing d002 was 3.46 °, and the volume specific electrical resistance was 3.0 Ω · cm. The obtained carbon fiber tow is solidified with epoxy resin and CF cross-sectional area is about 1.1m
An m ² string-like carbon fiber bundle was produced. Comparative Example 1 A spinning pitch having an optical anisotropy of 98%, a Mettler softening point of 298 ° C., a carbon content of 94% by weight, and an ash content of 50 ppm was spun at a die temperature of 333 ° C. while being bundled with a silicon-based oil agent. 11,000 pitch fiber tows having a length of 7000 m were obtained.

The obtained pitch fiber tow was heated to 380 ° C. at a heating rate of 1 ° C./min in the air and heated to perform infusibility treatment. Next, in a nitrogen gas atmosphere, the first carbonization treatment was performed at 530 ° C. and a residence time of 2 minutes without applying tension to the infusible fiber tow. The basis weight of the carbonized yarn obtained in the first carbonization treatment was 2.1 g / m. Further, in a nitrogen gas atmosphere, a tension of 1320 g / tow (120 g / 1000 strands) was applied to the first carbonized fiber tow, and
The second carbonization treatment was performed at a temperature of 3 ° C. and a residence time of 3 minutes to produce carbon fibers.

The carbon fiber obtained has a carbon content of 84%,
The hydrogen content was 2.5%, the graphite lattice constant Lc determined by X-ray diffraction was 20 °, and the interplanar spacing d002 was 3.44 °, and the volume specific electrical resistance was as high as 200Ω · cm. Comparative Example 2 A spinning pitch having an optical anisotropy of 100%, a Mettler softening point of 301 ° C., a carbon content of 96% by weight, and an ash content of 15 ppm was spun at a die temperature of 335 ° C. while being bundled with a silicon-based oil agent. 11,000 length 7000m
Was obtained.

The pitch fiber tow thus obtained was heated to 380 ° C. at a heating rate of 1 ° C./min in the air and heated to make it infusible. Next, in a nitrogen gas atmosphere, the first carbonization treatment was performed at 530 ° C. and a residence time of 2 minutes without applying tension to the infusible fiber tow. The basis weight of the carbonized yarn obtained in the first carbonization treatment was 2.1 g / m. Further, in a nitrogen gas atmosphere, a tension of 1320 g / tow (120 g / 1000 strands) was applied to the first carbonized fiber tow to 1200
The second carbonization treatment was performed at a temperature of 3 ° C. and a residence time of 3 minutes to produce carbon fibers.

The carbon fiber obtained has a carbon content of 99%,
The hydrogen content was <0.3%, the lattice constant Lc of graphite determined by X-ray diffraction was 27 °, and the interplanar spacing d002 was 3.47 °, and the volume specific electrical resistance was as low as 0.001Ω · cm.

[0034]

According to the present invention, carbon fibers and carbon fiber bundles having a high electric resistance can be produced, and these can be used as materials for preventing static electricity of electronic parts and the like, and radio waves such as outer wall materials of high-rise buildings. Since it can be suitably used as a material for absorption, it is industrially very useful.

Claims (5)

[Claims] 1. A volume specific electric resistance value of 10 ⁻² to 10 ² Ω.
cm, the carbon content is 85 to 95%, the hydrogen content is 0.3 to 2.5%, the lattice constant Lc of graphite obtained by X-ray diffraction is 25 ° or less, and the interplanar spacing d002 is 3.45.
炭素 Carbon fibers characterized by being long fibers. 2. A volume specific electric resistance value of 10 ⁻¹ to 10 Ω ·
2. The carbon fiber according to claim 1, wherein the diameter of the carbon fiber is 1 cm. 3. A volume electric resistance 10 ^-2 to 10 ² Omega
Cm, the carbon content is 85 to 95% or less, the hydrogen content is 0.3 to 2.5%, the lattice constant Lc of graphite obtained by X-ray diffraction is 25 ° or less, and the plane spacing d002 is 3 A carbon fiber aggregate comprising a plurality of long carbon fibers having an angle of 45 ° or more arranged in the length direction and bonded with a binder. 4. A volume specific electric resistance value of 10 ⁻¹ to 10 Ω ·
The carbon fiber aggregate according to claim 3, wherein the carbon fiber aggregate is cm. 5. The carbon fiber aggregate according to claim 3, wherein the total cross-sectional area of the carbon fibers of the carbon fiber aggregate is 0.2 to 80 mm ² .