WO1995025834A1 - Fibre de nitrure de bore et procede de production - Google Patents
Fibre de nitrure de bore et procede de production Download PDFInfo
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- WO1995025834A1 WO1995025834A1 PCT/JP1995/000500 JP9500500W WO9525834A1 WO 1995025834 A1 WO1995025834 A1 WO 1995025834A1 JP 9500500 W JP9500500 W JP 9500500W WO 9525834 A1 WO9525834 A1 WO 9525834A1
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- boron nitride
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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
- D01F9/10—Artificial filaments or the like of other substances; Manufacture thereof; Apparatus specially adapted for the manufacture of carbon filaments of inorganic material by decomposition of organic substances
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2916—Rod, strand, filament or fiber including boron or compound thereof [not as steel]
Definitions
- the present invention relates to a boron nitride fiber and a method for producing the same.
- the present invention relates to a boron nitride fiber and a method for producing the same. More specifically, the present invention relates to a boron nitride fiber having a higher tensile strength than any conventionally known boron nitride fiber and a method for producing the same.
- Boron nitride fibers are known. However, none of the conventionally known boron nitride fibers has a sufficiently high tensile strength, and no boron nitride fiber having a sufficiently high tensile strength has been known until now. Boron nitride fibers having sufficiently high tensile strength can be used, for example, as reinforcing fibers for ceramic materials.
- ceramic materials are high-strength and stable up to high temperatures, they are expected to be applied as high-temperature structural materials that cannot be replaced by plastic-metal materials. However, these materials are inherently brittle and fragile, contrary to their excellent thermal and mechanical properties. Due to the inherent brittleness of this material, the fracture of the ceramic occurs instantaneously. Therefore, these materials have not been widely used because they lack reliability as structural materials that are required to maintain a certain structure.
- As overcoming the brittleness of ceramics it is effective to enhance toughness by compounding with a reinforcing material. Spherical particles, plate-like particles, whiskers, continuous fibers, etc. are being studied as reinforcing materials to be composited. It is known that strengthening the toughness by compounding is effective and can increase the fracture toughness to the same level as aluminum alloy. Ceramic fibers and carbon fibers typified by silicon carbide fibers and alumina fibers are considered as candidates for continuous fibers for composite reinforcement.
- ceramic fibers have a polycrystalline structure in which fine crystals are aggregated, but when exposed to high temperatures, the constituent crystals become coarse and the tensile strength of the fibers is significantly reduced.
- carbon fiber the structural change at high temperature is small, and the tensile strength is maintained even when heated to about 2000 ° C.
- boron nitride fibers are unlikely to undergo structural changes such as crystal coarsening even at high temperatures unless they contain impurities such as boron oxide that promote crystal growth. It is estimated that the decrease in fiber tensile strength is small. That is, the thermal tension of the boron nitride fiber The decrease in strength is considered to be smaller than that of the ceramic fiber. Furthermore, boron nitride is stable to oxidation up to about 1000 ° C. in air, and has superior oxidation resistance to carbon fibers.
- boron nitride fibers have excellent properties as composite reinforcing fibers.
- boron nitride has low reactivity with other substances, as can be seen from its use in crucibles and mold release agents. Therefore, even if it is combined with various ceramics, it does not react with the mother phase, and it is considered that it is possible to form a composite.
- the improvement of fracture toughness of ceramics, which is a brittle material, due to the composite of continuous fibers is due to the mechanical energy applied to the composite material due to the phenomenon that the reinforcing fibers are pulled out of the matrix near the crack tip due to the bullet. Is thought to be absorbed.
- the boron nitride fiber has low reactivity with the parent phase, and thus often does not form a strong bond with the parent phase.
- boron nitride fiber is excellent in solid lubricity, when boron nitride fiber is used as a composite reinforcing fiber, pulling easily occurs, which is considered to have a great effect on improving fracture toughness.
- boron nitride fiber has excellent properties such as high electrical resistance, high thermal shock resistance, and high thermal conductivity in addition to the above-mentioned excellent properties as a reinforcing fiber. Material.
- a boron nitride precursor containing both boron and nitrogen is spun and then subjected to a heat treatment to thermally decompose the precursor fibers and convert them into boron nitride.
- a method hereinafter, also referred to as a precursor method
- a method hereinafter, also referred to as a nitriding method in which boron oxide fibers are heat-treated in an ammonia atmosphere to be nitrided are known.
- the precursor method involves spinning precursor fibers from a polycondensate of a borazine or borazine derivative, followed by heat treatment
- Japanese Patent Publication No. 53-37837 Japanese Patent Application Laid-Open No. 63-195173
- U.S. Patent No. 5,061,469 U.S. Patent No. 4,707,556; Chemistry of Materials, Volume 2, 96-97 (1990).
- a method in which a precursor fiber is spun from a borane and amine addition polymer, followed by heat treatment [Journal of the American Ceramic Society], Vol. 109, No. 5867 (1987).] Of the American Ceramic Society, Vol. 71, C 194 (1988).].
- the tensile strength of the obtained boron nitride fiber is measured by the methods described in JP-B-53-37837, JP-A-63-195173, and U.S. Pat. No. 5,061,469.
- Boron nitride that has not been subjected to heat stretching under the application of stress Fiber whose values are 784 MPa, 500 MPa, and 1200 MPa, respectively.
- These tensile strengths are lower than those of, for example, the tensile strength of carbon fiber of 300 OMPa or more, and no measures for increasing the strength are specifically indicated.
- studies using other precursor methods only show that it is possible to produce boron nitride fibers, and the physical properties such as tensile strength of the resulting boron nitride fibers were examined. Not.
- the tensile modulus of the boron nitride fiber is not significantly improved as compared with the tensile modulus of the boron nitride fiber obtained by the precursor method.
- the boron nitride fiber was reduced in diameter by drawing and had a fiber diameter of 6 ⁇ m or less, the maximum value of the tensile strength shown in the examples was 580 MPa, No significant improvement compared to the tensile strength of boron nitride fibers obtained by the precursor method o
- an object of the present invention is to provide a boron nitride fiber having a high tensile strength.
- a boron nitride fiber composed of boron nitride having a structure, wherein at least a part of the C plane is oriented substantially parallel to a fiber axis of the boron nitride fiber, and the degree of orientation of the C plane is Is achieved with boron nitride fibers having at least 0.74.
- a boron nitride precursor is formed by reacting an adduct of boron trihalide with a nitrile compound with ammonium halide or primary amine hydrohalide in the presence of boron trihalide.
- B dissolving the boron nitride precursor in a solvent to prepare a boron nitride precursor solution;
- Figure 1 shows the results obtained by heating boron nitride fibers treated with ammonia at 1800 ° C while applying tensile stress in a nitrogen gas atmosphere.
- 4 is a photograph of a diffraction image obtained by irradiating the boron nitride fiber of the present invention with X-rays from a direction perpendicular to the fiber axis.
- Fig. 2 shows the results obtained by heating boron nitride fibers treated with ammonia at 180 ° C in a nitrogen gas atmosphere without applying tensile stress.
- Fig. 2 is a photograph of a diffraction image obtained by irradiating X-rays from a direction perpendicular to the fiber axis.
- FIG. 3 shows an infrared absorption spectrum of the boron nitride fiber of the present invention by the KBr method.
- the present inventor has made intensive studies from various angles to achieve the above object. As a result, a hexagonal crystal, a rhombohedral crystal, and a boron nitride fiber in which the C-plane of boron nitride or turbostratic boron nitride was preferentially oriented in a direction parallel to the fiber were found. For the first time, it was found that the tensile strength was dramatically improved as the steel was highly oriented, and the present invention was completed here.
- the present invention relates to a boron nitride fiber and a method for producing the same. That is, the boron nitride fiber of the present invention has a surface (C surface) formed by connecting six-membered rings formed by alternately bonding boron and nitrogen in the plane direction of the six-membered rings. Is a boron nitride fiber composed of boron nitride having a laminated structure, and has a tensile strength of at least 140 OMPa. In the boron nitride fiber of the present invention, a surface (C surface) formed by connecting six-membered rings formed by alternately bonding boron and nitrogen in the surface direction of the six-membered rings is laminated.
- a boron nitride fiber comprising boron nitride having a structured structure, wherein at least a part of the C-plane is oriented substantially parallel to a fiber axis of the boron nitride fiber. And the degree of orientation of the C-plane is at least 0.74.
- the method for producing a boron nitride fiber of the present invention comprises:
- Boron nitride is a substance formed by the chemical bonding of boron in Group m of the periodic table with nitrogen in Group V of the periodic table.
- boron nitride having a structure formed by two-dimensional bonding of boron and nitrogen
- a six-membered ring formed by alternately bonding boron and nitrogen is connected in the plane direction of the six-membered ring
- boron nitride having a structure in which surfaces formed by stacking are stacked there is known.
- r-BN rhombohedral boron nitride
- the boron nitride fiber of the present invention has a structure in which the surfaces formed by connecting the six-membered rings formed by alternately bonding boron and nitrogen in the surface direction of the six-membered rings described above are laminated. Made of boron nitride.
- the boron nitride according to the present invention is composed of hexagonal boron nitride (h-BN), rhombohedral boron nitride (r-BN) and turbo- or turbostratic boron nitride (t-BN). It may be contained.
- hexagonal boron nitride (h-BN) and / or turboscopic boron nitride (t-BN) may constitute the main part of boron nitride.
- r-BN rhombohedral nitride
- turbostratic structure is a structure in which the C planes are stacked without regularity in the vertical direction, and is sometimes called a turbostratic structure.
- Both hexagonal boron nitride and turbostratic boron nitride can be confirmed by diffraction peaks from the (002) plane by X-ray diffraction.
- the crystal structure of both crystals is based on boron nitride such as a diffraction peak from the (110) plane by X-ray diffraction. It can be distinguished by the presence or absence of a diffraction peak due to symmetry in the direction perpendicular to the C plane of the crystal.
- the boron nitride fiber according to the present invention contains at least one of hexagonal boron nitride and turbostratic boron nitride, and includes hexagonal boron nitride and turbostratic boron nitride. In some cases.
- the crystallite diameter of the hexagonal crystal or turbostratic boron nitride constituting the boron nitride fiber is as very fine as 10 to 60 angstroms.
- the crystallite diameter indicates the size of the hexagonal crystal constituting boron nitride fiber and the C-plane in the laminating direction of boron nitride having a Z or turbostrate structure.
- the spacing between layers where the C-plane of hexagonal crystal and / or boron nitride having a turbostratic structure is stacked is about 3.3 ⁇ , so that a crystallite diameter of 10 to 60 ⁇ means that the C-plane Represents that boron nitride having a laminated structure of 3 to 20 layers is a structural unit.
- Boron nitride fiber of the present invention is to c generally crystallite hardly coarsened be exposed to high temperatures, hexagonal in boron nitride, if it contains boron oxide as an impurity, elementary boron nitride when heated to a high temperature crystal It is known that the child grows coarse.
- the reason why boron nitride fibers with fine crystallites can be obtained is that oxygen is not introduced in the raw materials and the manufacturing process, Therefore, it is considered that boron nitride fibers can be produced without containing boron oxide which promotes coarsening of crystallites.
- the C-plane of the above-mentioned hexagonal or turboscopic boron nitride is preferentially oriented in a direction parallel to the fiber axis of the boron nitride fiber.
- the boron nitride fibers obtained so far have a hexagonal or turbostratic boron nitride C-plane that is distributed isotropically with respect to the fiber axis.
- the present inventors have found boron nitride fibers in which the c-plane of hexagonal crystal or turbostratic boron nitride is oriented parallel to the fiber axis. Furthermore, it has also been found for the first time that when the degree of this orientation is improved, the tensile strength of the obtained boron nitride fiber is improved.
- the present inventor cannot fully explain why the orientation of the C plane of hexagonal or turbostratic boron nitride parallel to the fiber axis cannot improve the tensile strength, but it is estimated as follows. .
- hexagonal or turbostratic boron nitride the bond in the C plane is strongly covalent and the bond is strong, whereas the bond between the planes is mainly due to van der Perlska. It is considered a weak bond. Therefore, it is presumed that the tensile strength increases when the proportion of strong bonds in the C plane that are parallel to the fiber axis increases.
- the degree of orientation of the C-plane (hereinafter also referred to as the degree of orientation) is used as an index indicating the orientation distribution of the C-plane of hexagonal or turboscopic boron nitride with respect to the fiber axis of the boron nitride fiber.
- the boron nitride fiber according to the present invention is characterized in that the degree of orientation is 0.74 or more.
- the present inventor has also found boron nitride fibers having a degree of orientation of less than 0.4, and it is possible to produce them.
- boron nitride fibers having various degrees of orientation were manufactured and the tensile strength of the boron nitride fibers with respect to the degree of orientation was systematically examined, the tensile strength of the boron nitride fibers having an orientation of less than 0.5 was C
- the tensile strength of the boron nitride fiber whose plane is not preferentially oriented in the direction parallel to the fiber axis is substantially the same.
- the degree of orientation is 0.5 or more
- the tensile strength of the boron nitride fiber is significantly improved as compared with the tensile strength of the non-oriented boron nitride fiber.
- representative values show that the tensile strengths of boron nitride fibers having orientation degrees of 0.26 and 0.46 are both 44 OMPa, while the tensile strength of boron nitride fibers having an orientation degree of 0.80 is Was 1 97 OMPa.
- the degree of orientation is 0.7 or more
- the tensile strength of the boron nitride fiber increases substantially in proportion to the degree of orientation, when other conditions are kept constant.
- the tensile strength is 840 MPa when the degree of orientation is 0. 0, whereas the tensile strength is improved to 140 OMPa when the degree of orientation is 0.78. Therefore, when the degree of orientation is 0.70 or more, it is possible to further improve the tensile strength by improving the degree of orientation.
- the boron nitride fiber of the present invention has a tensile strength of at least 1400 MPa, Preferably at least 1660 MPa, more preferably at least 1870 MPa, more preferably at least 189 OMPa, even more preferably at least 1910 MPa, particularly preferably at least 1970 MPa, most preferably at least 2300 MPa belongs to.
- the above-mentioned tensile strength can be measured according to the “carbon fiber test method” specified in JISR 7601 (1986).
- the boron nitride fiber of the present invention has a degree of orientation of at least 0.74, preferably at least 0.78, more preferably at least 0.80, more preferably at least 0.81, and even more preferably at least 0.82. Particularly preferably at least 0.83, most preferably at least 0.86.
- the thermal conductivity in the fiber axis direction is higher when comparing the thermal conductivity in the in-plane direction and the thermal conductivity in the inter-plane direction of the six-membered carbon ring. It is known that, in the case of a carbon fiber in which a six-membered carbon ring is preferentially oriented in a direction parallel to the fiber axis, the thermal conductivity improves as the degree of orientation increases.
- the thermal conductivity of the boron nitride obtained by stacking the C-plane of boron nitride in a regular manner by the chemical vapor method was measured, and the thermal conductivity in the in-plane direction of the C-plane was measured. Is known to be nearly 100 times higher than the thermal conductivity in the direction perpendicular to the C plane. Therefore, it is considered that the boron nitride fiber having a high degree of orientation has higher thermal conductivity in the fiber axis direction than the boron nitride fiber having a low degree of orientation.
- the thermal conductivity of boron nitride is nearly ten times higher than that of alumina, mullite, silicon nitride, etc.
- compounding with boron nitride is performed for the purpose of improving the thermal conductivity of the material by using boron nitride fiber whose thermal conductivity in the fiber axis direction is improved by orientation. Can be improved.
- the degree of orientation described above can be determined by X-ray diffraction based on the X-ray intensity distribution on the Devy ring generated by diffraction from the C-plane of hexagonal crystal or turboscopic boron nitride.
- a method of measuring the degree of orientation by the X-ray diffraction method will be described.
- the X-rays to be used for diffraction use is made of copper K ⁇ rays (hereinafter referred to as Cu Ka rays) monochromated by a nickel filter, and the diffraction intensity is measured by a transmission method. It is desirable that the X-ray source be a point focus in order to obtain diffraction with high efficiency with respect to the X-ray output.
- boron nitride fibers Dozens or hundreds of bundles of boron nitride fibers are fixed with a small amount of collodion, etc., so that the boron nitride fibers are as parallel as possible, and used as a sample for X-ray diffraction. This is hereinafter referred to as an X-ray diffraction specimen.
- an X-ray diffraction specimen For the measurement of the diffraction intensity, either a method of photographing a diffraction image or a method using an X-ray diffractometer may be used.
- the fiber axis of the boron nitride fiber of the X-ray diffraction specimen is in a plane perpendicular to the incident X-ray, and the incident X-ray is Fix the X-ray diffraction specimen so that it irradiates the boron nitride fiber bundle of the X-ray diffraction specimen.
- the direction of the fiber axis of the boron nitride fiber of the X-ray diffraction specimen in a plane perpendicular to the incident X-ray can be in any direction as long as its relative direction to the diffraction image can be specified. Good. However, here, it is assumed that the fiber shaft is fixed vertically for explanation.
- the side opposite to the direction of the incident X-ray Install X-ray sensitive film.
- the X-ray sensitive film should be perpendicular to the direction of the incident X-ray.
- the distance from the X-ray diffraction specimen to the X-ray photosensitive film (hereinafter also referred to as the camera length) is determined by the hexagonal or turbostratic boron nitride constituting the boron nitride fiber of the X-ray diffraction specimen. The distance must be sufficient to capture the entire device ring due to diffraction from the C plane.
- the radius (D) of the device ring on the X-ray photosensitive film can be obtained by equation (1).
- L is the camera length
- 20 is the diffraction angle that satisfies the Bragg diffraction condition with respect to the C-plane of the hexagonal or turbostratic boron nitride constituting the boron nitride fiber of the X-ray diffraction specimen. It is.
- the camera length L may be set such that a circle having a radius D centered on the intersection of the direction of the incident X-ray and the X-ray sensitive film is included in the X-ray film.
- Diffraction X-ray intensity varies mainly depending on the amount of boron nitride fibers in the K piece for X-ray diffraction, and the crystallite diameter of the hexagonal or turbostratic boron nitride constituting the boron nitride fibers.
- the exposure time is too short, the SZN ratio of the degree of blackening due to diffraction X-rays of the X-ray photosensitive film decreases, and the error in the degree of orientation obtained increases.
- set the exposure time to the same X-ray diffraction sample. It is sufficient to take a diffraction image while changing the degree, and confirm that the obtained degree of orientation does not change.
- the intensity of diffracted X-rays can be determined by quantifying the degree of blackening of the film using a microdensitometer.
- the c-plane of the hexagonal or turbostratic boron nitride constituting the boron nitride fiber is oriented parallel to the fiber axis direction of the boron nitride fiber, the device photographed on the X-ray photosensitive film is used.
- a direction perpendicular to the fiber axis of the boron nitride fiber of the X-ray diffraction specimen passing through the center of the Debye ring (the intersection of the incident X-ray and the X-ray sensitive film) (hereinafter also referred to as the equatorial line direction)
- the equatorial line direction Of the film in the direction parallel to the fiber axis of the boron nitride of the X-ray diffraction specimen passing through the center of the Debye ring.
- the position of the diffraction intensity measurement point on the Devi ring is determined by the central angle ⁇ from the reference point on the Devi ring, and the intensity of the diffracted X-rays on the Devi ring is determined as a function.
- the X-ray intensity on the Devy ring is the sum of the intensity of the diffracted X-rays from the C-plane of the boron nitride fiber and the intensity of the background.
- the background X-ray intensity in the Debye ring is determined by measuring the X-ray intensity change in the radial direction of the Debye ring, and this is used as the X-ray intensity in the Debye ring.
- the intensity of the diffracted X-rays from the C plane is calculated as a function of the center angle ⁇ , two peaks having a maximum at the position corresponding to the equator direction are obtained. For each peak, the half width is measured in degrees, and the average (H) is calculated. Using the obtained H, the degree of crystal orientation () can be calculated by equation (2). Can be. [Edited by Carbon Society of Japan, "Development and Evaluation Method of Carbon Fibers", page 118 (1998).].
- An X-ray diffractometer can be used to measure the diffraction intensity.
- a known diffractometer can be used.
- a diffractometer in which the axis of the diffractometer is vertical and the scanning surface of the X-ray counter is horizontal will be described.
- a mechanism that can fix the X-ray diffraction specimen and rotate the X-ray diffraction specimen 360 degrees in a plane perpendicular to the incident X-rays is provided. Use a fiber sample stage that has it.
- the diffraction angle of the C-plane of the hexagonal crystal or turboscopic boron nitride constituting the boron nitride fiber of the X-ray diffraction specimen that satisfies the Bragg diffraction condition is determined by the transmission method.
- X-rays are incident, and the X-ray counter, that is, 2> of the diffractometer is scanned to measure the diffracted X-ray intensity.
- the angle at which the diffraction X-ray intensity shows the maximum in this angle range is determined. This angle is defined as the C-plane diffraction angle.
- fix the X-ray counter at the diffraction angle of the C plane inject X-rays, and place the X-ray diffraction specimen fixed on the fiber sample stage at 360 degrees in a plane perpendicular to the incident X-rays. Rotate and measure the corresponding diffracted X-ray intensity.
- the rotation angle of the X-ray diffraction specimen is ⁇ (however, the unit is degree), and ⁇ is 0 degree when the fiber axis of the boron nitride fiber of the X-ray diffraction specimen is vertical. ⁇ is 0 degree when the C-plane of hexagonal or turbostratic boron nitride constituting the boron nitride fiber of the X-ray diffraction specimen is oriented in the fiber axis direction of the boron nitride fiber. And diffracted to 180 degrees A peak having a maximum of X-ray intensity appears.
- the intensity of the diffracted X-rays needs to be corrected by subtracting the intensity of the background in the same manner as in the above-described method of taking a diffraction image on a photograph.
- the half-width of each peak is measured in degrees, and the average (H) can be used to calculate the degree of orientation (7 ⁇ ) from equation (2).
- the method for producing the boron nitride fiber of the present invention having a large tensile strength and a high degree of c-plane orientation is not particularly limited, but can be typically produced as follows.
- boron trihalide examples include boron trifluoride, boron trichloride, boron tribromide, boron triiodide and the like, and can be used without any particular limitation.
- nitrile compound a known compound having a nitrile group can be used without any particular limitation. Specifically, acetonitrile, propionitrile, forcepronitrile, acrylonitrile, crotonitolil, tonolenitrile, benzonitrile, i-butyronitrile, n-butyronitrile, isovaleronitrile, 2-methyl Examples include butyronitrile, pivonitrile, n-valeronitrile, malononitrile, succinonitrile, glutaronitrile, adiponitrile, pimeronitrile, suberonitrile and the like.
- the carbon contained in the boron nitride precursor is increased, and the desorption component when the boron nitride precursor is nitrided by heat treatment is increased.
- Cetonitrile with low carbon number And acrylonitrile are more preferably used.
- halogenated ammonium examples include ammonium fluoride, ammonium chloride, ammonium bromide, and ammonium iodide.
- Preferred examples of the halogenated ammonium include ammonium chloride.
- primary-grade hydrohalide As primary-grade hydrohalide, primary-amine hydrofluoride, —grade-amine hydrochloride, primary-amine hydrobromide, primary-amine hydroiodic acid Salts and the like can be mentioned.
- Preferred examples of the primary amine hydrohalide include primary amine hydrochloride (hereinafter also referred to as primary amine hydrochloride).
- Aquaamine hydrochloride is represented by the general formula, RNH 2 ⁇ HC1, where R is an alkyl group such as a methyl group, an ethyl group, or a propyl group, an aryl group such as a phenyl group, a tolyl group, or a xylyl group.
- R is an alkyl group such as a methyl group, an ethyl group, or a propyl group, an aryl group such as a phenyl group, a tolyl group, or a xylyl group.
- the compound which is a hydroxyl group is used without limitation. However, if the number of carbon atoms in R increases, the carbon contained in the boron nitride precursor increases, and the number of desorbed components when boron nitride is formed by heat treatment increases, so that R is a methyl group or an ethyl group. It is more preferable to use primary amine hydrochlor
- the above-mentioned adduct of boron trihalide and nitrile compound is reacted with ammonium halide or primary amine hydrohalide. Synthesize boron nitride precursor.
- the adduct of the boron trihalide and the nitrile compound is a product in which boron of halogenogen is addition-bonded to a non-bonded electron pair of a nitrogen atom of a nitrile group. Easily reacts with boron nitride and nitrile compounds To produce this adduct.
- the method for producing the adduct is not particularly limited.
- a method of dropping boron trihalide into a solution of a nitrile compound in an organic solvent at room temperature a method of dissolving a nitrile compound in an organic solvent and then blowing boron trihalide, or a method of blowing boron trihalide into the organic solvent
- An adduct can be formed by, for example, dissolving boron trihalide and then dropping a nitrile compound. Since the boron trihalide and the nitrile compound easily react to form an adduct, they may be brought into contact with each other immediately before the reaction.
- boron trihalide is present during the reaction of the above adduct with ammonium halide or primary ammonium halide.
- boron triboride is not present during the reaction, the yield of the boron nitride precursor is low, and a spinning solvent for spinning described later, for example, N, N-dimethylformamide (hereinafter also referred to as DMF) Insoluble reaction by-products are produced.
- DMF N, N-dimethylformamide
- the boron trihalide may be present at least during the reaction of an adduct of boron trihalide and a nitrile compound with an ammonium halide or a primary ammonium hydrohalide.
- an excess amount of boron trihalide is used so that unreacted boron trihalide and adduct coexist in advance. You may have.
- the amount of boron trihalide to be added to the nitrile compound can be arbitrarily selected from a range of 1.05 to 2.00 in molar ratio (boron trinitrile compound).
- the molar ratio of boron trihalide to nitrile compound is preferably 1.1 to 1.5. At this time, the boron trihalide and nitrile compound form a one-to-one adduct, and the amount of boron trihalide present during the reaction is determined by the molar ratio (boron trihalide Z (Additive) in the range of 0.1 to 0.5.
- the concentration of the nitrile compound with respect to the reaction solvent is not particularly limited, but is preferably in the range of 0.1 to 10 mol / l. If the concentration of the nitrile compound is less than 0.1 mo 1/1, the amount of the obtained boron nitride precursor is small, which is not preferable because it is not efficient. On the other hand, when the concentration of the nitrile compound exceeds 1 Omo 1/1, the amount of the adduct formed as a solid with respect to the solvent becomes too large, and the formation of the adduct becomes ununiform.
- the amount of the ammonium halide or primary amine hydrohalide added is in the range of 0.67 to 1.5 in terms of the molar ratio to the nitrile compound (ammonium halide or -grade ammonium hydrohalide Z ditolyl compound). It is preferable to select more. If the amount of ammonium halide or primary ammonium hydride is high, a component insoluble in DMF is generated, and if the amount of nitrile compound is higher, the amount of unreacted adduct tends to increase. 0.83 or more: It is better to select from the range of I.2.
- the solvent used for synthesizing the boron nitride precursor of the present invention is not particularly limited, but when the boron nitride precursor which is a reaction product is separated, a borazine compound or the like which is a reaction by-product is dissolved. It is preferable that it be easily removed. From such a viewpoint, an organic solvent such as benzene, toluene, xylene, and benzene is preferably selected.
- the heating temperature for reacting the adduct with the ammonium halide or primary amine hydrohalide generally requires a long time for the reaction at low temperatures, and increases the components insoluble in DMF at high temperatures and lowers the reaction yield. I do. Therefore, the heating temperature may be selected from the range of 100 ° C to 160 ° C.
- the heating time varies depending on the temperature, but may be selected from the range of 3 to 30 hours.
- the boron nitride precursor is formed as an orange or brown precipitate.
- reaction device for obtaining the boron nitride precursor a known device is used without any particular limitation.
- both the adduct of boron trihalide and nitrile compound and the boron nitride precursor are hydrolyzed, so the reaction system must be sufficiently dried beforehand with nitrogen gas, etc. It is necessary to provide a moisture absorbent such as calcium chloride at the opening of the equipment to prevent moisture in the air from entering from outside.
- step (b) The boron nitride precursor generated in step (a) is dissolved in a solvent to prepare a boron nitride precursor solution.
- This boron nitride precursor solution can be used as a spinning solution in the next step (C).
- a known method can be used without particular limitation.
- the spinning solution is prepared by dissolving the boron nitride precursor in a soluble solvent.
- the precursor soluble solvent include DMF, ⁇ -caprolactam, chloronitrile, malonitrile, ⁇ -methyl-, ⁇ -cyanoethylformamide, ⁇ , ⁇ -methylformamide and the like. it can.
- Boron nitride precursor By dissolving in a soluble solvent, an orange or brown transparent spinning solution can be obtained.
- the viscosity of the spinning solution can be adjusted as desired, for example, by adding an acrylonitrile-based polymer.
- the viscosity of the spinning solution is increased by using an acrylonitrile-based polymer having a relatively high molecular weight together with the boron nitride precursor to improve the spinnability of the spinning solution. can do.
- the acrylonitrile-based polymer used in the present invention can be used without any particular limitation as long as it is dissolved in the soluble solvent constituting the spinning solution and does not cause phase separation with the boron nitride precursor in the spinning solution.
- it is a polymer of acrylonitrile or a polymerizable monomer other than acrylonitrile having a vinyl group such as vinyl acetate, atarylamide, methacrylic acid, methacrylic acid ester, acrylic acid, acrylate ester (hereinafter simply referred to as vinyl monomer). ) And acrylonitrile.
- acrylonitrile constituting the copolymer is preferably 85 mol% or more based on the total polymerizable monomer.
- the above-mentioned vinyl monomer contains an oxygen atom, but has an adverse effect on the boron nitride fiber from which the oxygen atom is obtained, such as coarsening the boron nitride crystal and reducing the strength of the boron nitride fiber. It can have an effect. Therefore, a more preferred acrylonitrile-based polymer is an acrylonitrile homopolymer.
- the weight average molecular weight of the acrylonitrile polymer used in the present invention is particularly although not limited, it is preferably in the range of 10,000 to 2,000,000.
- the amount of the acrylonitrile polymer to be added to the spinning solution is not particularly limited, but is preferably 0.01 to 5 parts by weight based on 100 parts by weight of the boron nitride precursor.
- step (c) spinning the boron nitride precursor solution prepared in step (b) to form boron nitride precursor fibers.
- the preferred concentration range of the spinning solution is from 0.01 to 3.0 g "m1, and the viscosity at that time is from 10 to 100,000 poise, depending on the spinning method.
- Boron nitride precursor fiber is obtained from the obtained spinning solution.
- a widely known spinning method can be used, for example, a method of discharging a spinning solution by using a centrifugal force by rotating a container having a small hole containing a spinning solution.
- the boron nitride precursor fiber can be spun by a method of discharging the spinning solution by gas pressure, a method of discharging the spinning solution from a small hole using a gear pump, or the like.
- the spinning temperature may vary depending on the solvent used, but is, for example, from ⁇ 60 to 200 ° C., preferably from 1 to 10: 80 ° C., and more preferably from 0 to 160 ° C.
- the boron nitride precursor fiber obtained in the above step (c) is heat-treated (preheated) at 100 to 600 ° C under an inert gas atmosphere, and then at 200 to 1300 ° C under an ammonia gas atmosphere. Heat treatment Thereby, boron nitride fibers are obtained.
- the boron nitride fiber at this stage is hereinafter referred to as an unoriented boron nitride fiber.
- unoriented boron nitride fiber When producing unoriented boron nitride fibers, if only heat treatment is performed in an inert atmosphere, carbon derived from the boron nitride precursor cannot be removed, and the resulting fibers exhibit a black color.
- the resulting boron nitride fiber will have a large boron nitride crystallite diameter, and will have defects and scratches on the fiber surface, resulting in a high-strength nitride. Unable to obtain raw fibers.
- Nitrogen, argon, helium, or the like can be used as an atmosphere gas in the heat treatment under an inert gas atmosphere.
- the heat treatment temperature in the heat treatment under an inert gas atmosphere is 100 to 600 ° C., preferably 150 to 55 ° C., and more preferably 160 to 500 ° C. You can arbitrarily select from the range. If this heat treatment is performed at a temperature lower than 100 ° C., the subsequent heat treatment in an atmosphere of ammonia gas will increase the crystallite diameter of boron nitride and generate defects and scratches on the fiber surface. At best, the strength of the fiber may be reduced.
- the heating device for heating the boron nitride precursor fiber in an inert gas atmosphere may have any structure capable of controlling the atmosphere with a single chamber or a furnace tube, such as an electric furnace or a gas furnace.
- a known heating device can be used without any particular limitation.
- the heat treatment method is a batch-type heat treatment in which a certain amount of boron nitride precursor fibers are heat-treated at once, and a continuous boron nitride precursor fiber is sequentially sent to a heating device that has been heated to the heat treatment temperature in advance.
- Heat treatment and heating There is a continuous heat treatment in which the treated fiber is wound up and collected, and any heat treatment method may be used in the present invention.
- heat treatment may be performed by introducing boron nitride precursor fibers into a heat treatment device which has been heated to the heat treatment temperature in advance, or a heat treatment device. After the boron nitride precursor fiber is placed in the furnace, the temperature is raised to reach the heat treatment temperature, and the heat treatment can be performed.
- the solvent for producing a spinning solution from the boron nitride precursor such as DMF
- the holding time at the heat treatment temperature can be arbitrarily selected from the range of 0 to 10 hours.
- the holding time of 0 hours means that immediately after the boron nitride precursor fiber reaches the heat treatment temperature, the heating device is cooled down or the boron nitride precursor fiber is taken out of the heating device to end the heat treatment.
- the heat treatment atmosphere in the heat treatment under an inert gas atmosphere may be any of a temperature rising process until the heat treatment temperature is reached, a holding process at the heat treatment temperature, and a temperature decrease process until the heat treatment is completed.
- the inert gas atmosphere is preferably used while the boron nitride precursor fiber is in a chamber of a heating device, a furnace tube, or the like in an inert gas atmosphere.
- the chamber of the heating device replaced with the inert gas, the furnace tube, and the like may be sealed, or the inert gas may be circulated through the chamber, the furnace tube, and the like of the heating device.
- a heat treatment in an ammonia gas atmosphere is performed.
- the temperature of the heat treatment in the atmosphere of the ammonia gas can be arbitrarily selected from the range of 200 to 130 ° C. If the heat treatment in an ammonia gas atmosphere is performed at a temperature lower than 200 ° C, the carbon derived from the precursor is not sufficiently removed, and 5 to 15% by weight of carbon remains in the boron nitride fiber. Resulting in.
- the precursor can be obtained by heating at a temperature of 200 to 130 ° C., preferably 250 to 125 ° C., more preferably 300 to 1200 ° C. Since carbon derived from the body is substantially decomposed and removed, it is not particularly necessary to perform the heat treatment in an ammonia gas atmosphere at a temperature higher than 130 ° C.
- the heating device for heating the boron nitride precursor fiber in a gaseous atmosphere may have a structure capable of controlling the atmosphere with a chamber or a furnace tube, and may be a known device such as an electric furnace or a gas furnace. The heating device is used without any particular limitation.
- any of a batch heat treatment method and a continuous heat treatment method may be used as in the heat treatment under an inert gas atmosphere.
- heat treatment is performed by introducing the boron nitride precursor fiber into a heat treatment device preheated to the heat treatment temperature, or heating the boron nitride precursor fiber. After the heat treatment is performed, the temperature is raised to reach the heat treatment temperature and the heat treatment is performed.
- thermal decomposition products are rapidly desorbed, resulting in defects such as voids and cracks in the obtained boron nitride fiber, and the strength is increased. May be reduced.
- the heat treatment at a heating rate of 20 V / min or less until the boron nitride precursor fiber reaches the heat treatment temperature.
- the holding time at the heat treatment temperature also depends on the amount of the boron nitride precursor fiber to be heat-treated.
- the holding time of 0 hours means that immediately after the boron nitride precursor fiber reaches the heat treatment temperature, the heating device is cooled down, or the boron nitride precursor fiber is removed from the heating device and the heat treatment is completed. Is shown.
- the heat treatment atmosphere be an ammonia gas because the heat treatment temperature performed in an inert gas atmosphere during the temperature rise process is changed from the heat treatment temperature in an ammonia gas atmosphere. This is a holding process at a heat treatment temperature in an atmosphere of ammonia gas until the temperature reaches the temperature.
- an inert gas atmosphere such as nitrogen, argon, helium, or the like is used. Any of the ammonia gas atmospheres may be used.
- the chamber and the furnace tube of the heating device replaced with the ammonia gas may be sealed, or the ammonia gas may be circulated through the chamber and the furnace tube of the heating device.
- the heat treatment preliminary heating
- the heat treatment in an ammonia atmosphere it is preferable to first perform the heat treatment (preliminary heating) in an inert gas atmosphere, and then perform the heat treatment in an ammonia atmosphere.
- first perform a heat treatment in an inert gas atmosphere and the heat treatment in an ammonia gas atmosphere sequentially, first perform a heat treatment in an inert gas atmosphere, and then complete the heat treatment in an inert gas atmosphere.
- the atmosphere gas may be changed to ammonia and the heat treatment may be performed in an ammonia gas atmosphere, or the heat treatment may be performed in an inert gas atmosphere by lowering the temperature of the heat treatment or removing boron nitride fibers from a heating device. After completion of the heat treatment, the heat treatment may be performed again in an atmosphere of ammonia gas.
- the boron nitride fiber of the present invention can be obtained by heating the fiber treated with ammonia obtained in the above step (e) at 1600 to 2300 ° C while applying a tensile stress in an inert gas atmosphere. .
- Boron nitride fiber having a degree of orientation of 0.74 or more is obtained by applying unstretched boron nitride fiber under an inert gas atmosphere while applying tensile stress to the fiber at 1600 to 2300 ° C, preferably 1650 to 2250 ° C. Preferably, it can be obtained by performing a heat treatment at 1700 to 2200 ° C (hereinafter also referred to as an orientation treatment).
- the atmosphere in the orientation treatment is not particularly limited as long as the boron nitride is not chemically modified such as oxidation. Accordingly, an inert gas such as, for example, nitrogen, argon, or helium can be used as an atmosphere gas during the orientation treatment. Alternatively, the orientation treatment can be performed under vacuum.
- the heat treatment temperature in the orientation treatment can be arbitrarily selected from the range of 1600 to 2300 ° C. If the heat treatment temperature is lower than 1600 ° C, the orientation may not sufficiently proceed even when a tensile stress is applied, and the degree of orientation may not reach 0.74. In addition, since the decomposition reaction of boron nitride starts at 2300 ° C. or higher, it is not preferable to perform the heat treatment at 2300 ° C. or higher.
- a heating device for performing the orientation treatment may be any device having a structure in which the atmosphere can be controlled by a chamber or a furnace tube, and a known heating device such as an electric furnace or a gas furnace is used without any particular limitation.
- the orientation treatment is a batch-type treatment in which a certain amount of unoriented boron nitride fibers are treated at one time, and the continuous unoriented boron nitride fibers are continuously fed to a heating device heated to the heat treatment temperature in advance. And then take up the treated fiber and collect it. There is continuous processing, and any of the processing methods may be used in the present invention.
- the non-oriented boron nitride fiber is introduced into a heating device that has been heated to the heating treatment temperature in advance, or the heat treatment is performed. After being placed in the heat treatment device, the temperature is raised to reach the heat treatment temperature and the heat treatment is performed.
- the orientation treatment if the unoriented boron nitride fiber is heated rapidly, a defect may occur due to thermal stress, and the strength of the obtained boron nitride fiber may decrease. Therefore, it is preferable to perform the orientation treatment at a rate at which the unoriented boron nitride fiber reaches the heat treatment temperature of 100 ° CZmin or less.
- the holding time at the heat treatment temperature can be arbitrarily selected from the range of 0 to 10 hours, depending on the amount of the unoriented boron nitride fibers to be subjected to the heat treatment and the heat treatment temperature.
- the holding time of 0 hours means that immediately after the unoriented boron nitride fiber reaches the heat treatment temperature, the heating device is cooled down or the unoriented boron nitride fiber is taken out of the heating device and the heating process is completed.
- the atmosphere in the orientation treatment is an inert gas atmosphere or a vacuum during any process of heating up to the heat treatment temperature, holding at the heat treatment temperature, and cooling down to the end of the heat treatment. Is preferred.
- the chamber of the heating device replaced with the inert gas, the furnace tube, etc. may be sealed, or the inert gas may be passed through the chamber of the heating device, the furnace tube, etc. .
- the method of applying a tensile stress to the unoriented boron nitride fibers is not particularly limited.
- the unoriented boron nitride fibers are vertically Hanging in the direction, and adding a weight to the lower end, a tensile stress can be applied.
- unoriented When boron nitride fiber is heated to 1600 to 2300 ° C in an inert gas atmosphere without applying tensile stress, it shrinks in the fiber axis direction depending on the heating temperature.
- a formwork made of a material such as boron nitride that does not react with the unoriented boron nitride fiber is attached to the unoriented boron nitride fiber, and is directly heated to 1600 to 2300 ° C in an inert gas atmosphere. If the heat treatment is performed in such a manner, the heat shrinkage of the unoriented boron nitride fiber due to the heat treatment is prevented by the mold, and as a result, the heat treatment can be performed while applying a tensile stress to the unoriented boron nitride fiber.
- the unoriented orientation is controlled by controlling the supply speed of the unoriented boron nitride fiber to the heat treatment device and the winding speed of the heat-treated fiber.
- the heat shrinkage of the boron nitride fiber during the heat treatment can be controlled, and as a result, the heat treatment can be performed while applying a tensile stress.
- the tensile stress applied to the unoriented boron nitride fibers in the orientation treatment depends on the heat treatment temperature and heat treatment time of the orientation treatment, but when the stress is applied by suspending a weight, etc. It can be arbitrarily selected within the range of 1000MPa. If the applied stress is smaller than 0.1 MPa, the orientation may be insufficient and the degree of orientation may not reach 0.74. If the applied stress is larger than 100 OMPa, the unoriented fiber may be broken.
- the stretching ratio is For example, it may be selected from the range of 10 to 32%. However, the stretching ratio (E) is calculated by the formula (3) Defined by
- L f is the fiber when heat-treated at the heat treatment temperature (T ° C) without limiting the thermal shrinkage of the unit length boron nitride fiber, that is, without applying tensile stress to the boron nitride fiber.
- Ls represents the length of the fiber sample when the unit length of boron nitride fiber is heat-treated to the heat treatment temperature (T ° C) while restricting the heat shrinkage.
- the elongation is less than 10%, the tensile stress applied to the unoriented boron nitride fiber is insufficient, and there is a case where the degree of orientation does not reach 0.74. If the stretching ratio is larger than 32%, the unoriented boron nitride fiber may break during the orientation process.
- the oriented boron nitride fiber produced in this way has a feature that, in addition to the fineness of the crystallites of the constituent boron nitride, it is white and glossy.
- the method for producing the boron nitride fiber of the present invention is obtained, for example, by reacting an adduct of boron trichloride with a nitrile compound having 3 or less carbon atoms and ammonium chloride in the presence of boron trichloride.
- the boron nitride precursor is dissolved in N, N-dimethylformamide solvent, and the solution is spun, and then heat-treated at 100 to 600 ° C. in an inert gas atmosphere, and then in an ammonia gas atmosphere.
- Boron fibers can be produced.
- a boron nitride fiber having significantly improved tensile strength can be manufactured.
- the fiber tensile strength is an important factor in the degree of C-plane orientation, it is easily affected by surface defects and scratches due to differences in spinning methods. Therefore, a change in tensile strength due to a change in the degree of orientation when manufactured under the same conditions is important in the present invention.
- the yield of the boron nitride precursor was determined based on the amount of boron (B) in the raw material boron trihalide.
- the two cold fingers were filled with dry ice and one acetone, and while stirring with a stirrer, 60 g of boron trichloride was condensed and dropped from the cold finger directly attached to the three-necked flask over 2 hours. This produced a white boron trichloride-acetonitrile adduct.
- the cold finger directly attached to the three-necked flask was removed, and 21.5 g of ammonium chloride dried at 110 ° C overnight was added.
- the suspension was heated to 125 ° C for 8 hours with little evolution of hydrogen chloride and a brown precipitate formed.
- the resulting precipitate was separated by filtration, washed with benzene (10 Om1), and dried under reduced pressure to obtain 24 g (83% yield) of a boron nitride precursor.
- the spun boron nitride precursor fiber is heated at a rate of l ° CZm i in a nitrogen stream.
- the temperature was raised from room temperature to 400 ° C. at n, and after reaching 400 ° C., the mixture was allowed to cool to room temperature and heat-treated.
- the temperature is raised from room temperature to 1000 ° C at a rate of 2 ° C / min, and after reaching 1000 ° C, it is cooled to 500 ° C at a cooling rate of 5 ° C / min, and then to room temperature. Heat treatment was performed after cooling.
- an unoriented boron nitride fiber having a diameter of about 15 m was obtained.
- the unoriented boron nitride fiber is wound into a loop with a circumference of 122 mm, and is hung on a boron nitride formwork with a circumference of 103 mm while maintaining the loop shape, and is directly heated in a nitrogen stream at a heating rate of 10 ° CZm. In, raise the temperature from room temperature to 1800 ° C, hold at 1800 ° C for 30 minutes, cool to 500 ° C at a cooling rate of 5 ° C / min, and then allow to cool to room temperature to perform orientation treatment Was. After the treatment, the boron nitride fiber remained wound around the form without breaking or unraveling. At this time, the stretching ratio was 12.7%. The degree of orientation of the obtained boron nitride fiber was 0.8, and the tensile strength was 140 OMPa.
- FIG. 1 shows a photograph of a diffraction image observed when the boron nitride fiber was irradiated with X-rays (CuKa, 50 kV, 24 mA) from a direction perpendicular to the fiber axis.
- FIG. 3 shows the infrared absorption spectrum (KBr) of the boron nitride fiber.
- the unoriented boron nitride fiber produced in the same manner as in Example 1 was wound into a loop having a circumference of 122 mm, and while maintaining the loop shape, was hung on a boron nitride formwork having a circumference of 103 mm, and nitrogen was used as it was.
- the temperature is raised from room temperature to 2000 ° C at a rate of 10 ° C / min, held at 2000 ° C for 30 minutes, and cooled. It was cooled to 500 ° C at a cooling rate of 5 ° CZmin, and then allowed to cool to room temperature for orientation treatment. After the treatment, the boron nitride fiber remained wound around the form without breaking or unraveling.
- the stretching ratio at this time was 15.7%.
- the degree of orientation of the obtained boron nitride fiber was 0.74, and the tensile strength was 1660 MPa.
- An unoriented boron nitride fiber produced in the same manner as in Example 1 was wound into a loop of 122 mm around the circumference, and while maintaining the loop shape, was hung on a boron nitride formwork with a circumference of 107 mm.
- the boron nitride fiber remained wound around the form without breaking or unraveling.
- the stretching ratio at this time was 20.2%.
- the degree of orientation of the obtained boron nitride fiber was 0.80, and the tensile strength was 1970 MPa.
- the unoriented boron nitride fiber produced in the same manner as in Example 1 was wound into a loop having a circumference of 122 mm, and, while maintaining the loop shape, was hung on a boron nitride formwork having a circumference of 111 mm.
- a heating rate l O ⁇ Zmin Hold at 2000 ° C for 30 minutes, cool to 500 ° C at a cooling rate of 5 ° CZin, then cool to room temperature And performed orientation processing.
- the boron nitride fiber remained wound around the form without breaking or unraveling. At this time, the stretching ratio was 24.7%.
- the degree of orientation of the obtained boron nitride fiber is 0.86 and the tensile strength is 23 It was 0 OMPa.
- the unoriented boron nitride fiber produced in the same manner as in Example 1 is wound into a loop of 122 mm in circumference, and while maintaining the loop shape, hung on a boron nitride formwork of 95 mm in circumference, and the nitrogen stream is passed as it is.
- An orientation treatment was performed. After the treatment, the boron nitride fiber remained wound around the form without breaking. The stretching ratio at this time was 6.7%.
- the obtained boron nitride fiber has a degree of orientation of 0.66 and a tensile strength of 100 OMPa.
- the unoriented boron nitride fiber produced in the same manner as in Example 1 was wound into a loop having a circumference of 122 mm, and the loop was maintained.
- the temperature is raised from room temperature to 1800 ° C at a heating rate of 10 D CZmin, maintained at 1800 ° C for 30 minutes, cooled to 500 ° C at a cooling rate of ⁇ ⁇ ⁇ i ⁇ , and then allowed to cool to room temperature Then, an orientation treatment was performed. After the treatment, the boron nitride fiber remained wound around the form without breaking.
- the stretching ratio at this time was 7.1%.
- the degree of orientation of the obtained boron nitride fiber was 0.70, and the tensile strength was 84 OMPa.
- the unoriented boron nitride fiber produced in the same manner as in Example 1 was wound into a loop having a circumference of 122 mm, and a loop having a circumference of 98 mm was maintained while maintaining the loop shape. Hung on a boron nitride formwork, as it is, in a nitrogen stream, the temperature was raised from room temperature to 1600 ° C at a temperature rise rate of 10 ° CZin, held at 1 600 ° C for 30 minutes, and cooled at a cooling rate of 5 ° CZin in 500 The solution was cooled to ° C and then allowed to cool to room temperature to perform an orientation treatment. After the treatment, the boron nitride fiber remained wound around the form without breaking. At this time, the stretching ratio was 3.3%. The degree of orientation of the obtained boron nitride fiber is 0.46 and the tensile strength is 440 MPa.
- the unoriented boron nitride fiber produced in the same manner as in Example 1 was heated from room temperature to 1800 ° C at a rate of 10 ⁇ Zin in a nitrogen stream without applying tensile stress to the fiber. Then, it was kept at 1800 ° C for 30 minutes, cooled to 500 ° C at a cooling rate of 5 ° C Zmin, and then allowed to cool to room temperature to perform an orientation treatment.
- the degree of orientation of the obtained boron nitride fiber was 0.35, and the tensile strength was 450 MPa.
- FIG. 2 shows a photograph of a diffraction image observed when the boron nitride fiber was irradiated with X-rays (CuK, 50 kV, 24 mA) from a direction perpendicular to the fiber axis.
- the unoriented boron nitride fiber produced in the same manner as in Example 1 was heated from room temperature to 1600 ° C at a rate of 10 ° CZmin in a nitrogen stream without applying tensile stress to the fiber.
- the temperature was kept at 1,600 ° C for 30 minutes, cooled to 500 ° C at a cooling rate of 5 ° C / in, and then allowed to cool to room temperature to perform an orientation treatment.
- the degree of orientation of the obtained boron nitride fiber was 0.26, and the tensile strength was 440 MPa. Comparative Example 6
- the non-oriented boron nitride fiber produced in the same manner as in Example 1 was heated from room temperature to 2000 ° C at a rate of 10 ° CZmin in a nitrogen stream without applying tensile stress to the fiber.
- the temperature was kept at 2000 ° C for 30 minutes, cooled to 500 ° C at a cooling rate of 5 ° C / min, and then allowed to cool to room temperature to perform an orientation treatment.
- the degree of orientation of the obtained boron nitride fiber was 0.37, and the tensile strength was 47 OMPa.
- Boron nitride precursor fiber prepared in the same manner as in Example 1 was placed in a nitrogen stream. The temperature was raised from room temperature to 400 ° C at a rate of l ° CZmin, and then cooled to room temperature after reaching 400 ° C. Then, a heat treatment was performed. Next, in an ammonia gas atmosphere, the temperature was raised from room temperature to 400 ° C. at a temperature rising rate of 2 ° 111 in, and after reaching 400 ° C., it was allowed to cool to room temperature and heat-treated. Thus, an unoriented boron nitride fiber was obtained.
- This unoriented boron nitride fiber was oriented in the same manner as in Example 3. At this time, the draw ratio was 20.2%, the orientation degree of the obtained boron nitride fiber was 0.82, and the tensile strength was 193 OMPa.
- Boron nitride precursor fiber produced in the same manner as in Example 1 was heated from room temperature to 400 ° C at a rate of 1 ⁇ Zmin in a nitrogen stream, and allowed to cool to room temperature after reaching 400 ° C. Then, a heat treatment was performed. Then, in an ammonia gas atmosphere, the temperature is raised from room temperature to 800 ° C at a temperature rising rate of 2 ° C / min, and after reaching 800 ° C, it is cooled to 500 ° C at a cooling rate of 5 ° CZin, and then It was left to cool to room temperature and was subjected to a heat treatment. This results in unoriented boron nitride Fiber was obtained.
- This unoriented boron nitride fiber was oriented in the same manner as in Example 3. At this time, the stretching ratio was 20.3%, the orientation degree of the obtained boron nitride fiber was 0.83, and the tensile strength was 191 OMPa.
- the boron nitride precursor fiber produced in the same manner as in Example 1 was heated from room temperature to 400 ° C at a heating rate of l ° CZmin in a nitrogen stream, and allowed to cool to room temperature after reaching 400 ° C. Then, a heat treatment was performed. Then, in an ammonia gas atmosphere, the temperature is raised from room temperature to 1200 ° C at a heating rate of 2 ° CZin, and after reaching 1200 ° C, it is cooled to 500 ° C at a cooling rate of 5 ° CZin, and then cooled to room temperature. The mixture was allowed to cool and subjected to heat treatment. Thus, an unoriented silicon nitride fiber was obtained.
- This unoriented boron nitride fiber was oriented in the same manner as in Example 3. At this time, the stretching ratio was 20.1%, the orientation degree of the obtained boron nitride fiber was 0.82, and the tensile strength was 188 OMPa.
- the boron nitride precursor fiber produced in the same manner as in Example 1 was heated from room temperature to 200 ° C at a heating rate of 1 ° C Zmin in a nitrogen stream, and allowed to cool to room temperature after reaching 200 ° C. Then, a heat treatment was performed. Next, in an ammonia gas atmosphere, The temperature was raised from room temperature to 1000 ° C. in 1000 ° C., and after reaching 10000 ° C., cooling was performed at a cooling rate of 5 ° C. Z in to 500, and then allowed to cool to room temperature to perform a heat treatment. As a result, unoriented boron nitride fibers were obtained.
- This unoriented boron nitride fiber was oriented in the same manner as in Example 3. Was. At this time, the draw ratio was 20.2%, the orientation of the obtained boron nitride fiber was 0.82, and the tensile strength was 189 OMPa.
- a stirrer was attached to the middle tube of a three-neck flask with a capacity of 1 liter, a dropping funnel containing 128 g of boron tribromide in one of the side tubes, and a ball-in cooling tube for the remaining side tubes.
- a calcium chloride tube was attached to the outlet of the ball-in cooling tube.
- the spun boron nitride precursor fiber was subjected to a heat treatment at 400 ° C. in a nitrogen stream and then at 1000 ° C. in an ammonia gas atmosphere in the same manner as in Example 1.
- An unoriented boron nitride fiber having a diameter of about 15 ⁇ was obtained.
- This unoriented boron nitride fiber was oriented in the same manner as in Example 3. At this time, the draw ratio was 20.2%, the orientation degree of the obtained boron nitride fiber was 0.81, and the tensile strength was 187 OMPa.
- a stirrer was attached to the middle tube of a three-neck flask with a capacity of 1 liter, a dropping funnel containing 16.4 g of acetonitrile in one of the side tubes, and a ball-in cooling tube to the remaining side tubes.
- a calcium chloride tube was attached to the outlet of the ball-in cooling tube.
- the spun boron nitride precursor fiber is subjected to a heat treatment in a nitrogen stream at 400 ° C. and then in an ammonia gas atmosphere at 1000 ° C. in the same manner as in Example 1 to obtain an unoriented boron nitride having a diameter of about 15 m. Fiber was obtained.
- This unoriented boron nitride fiber was subjected to an orientation treatment in the same manner as in Example 3. At this time, the draw ratio was 20.1%, the degree of orientation of the obtained boron nitride fiber was 0.81, and the tensile strength was 188 OMPa.
- the spun boron nitride precursor fiber is subjected to a heat treatment at 400 ° C. in a nitrogen gas stream and then at 1000 ° C. in an ammonia gas atmosphere in the same manner as in Example 1 to obtain an unoriented boron nitride fiber having a diameter of about 15 m. An elementary fiber was obtained.
- This unoriented boron nitride fiber was subjected to an orientation treatment in the same manner as in Example 3. At this time, the draw ratio was 20.2%, the degree of orientation of the obtained boron nitride fiber was 0.82, and the tensile strength was 190 OMPa.
- the spun boron nitride precursor fiber is subjected to a heat treatment in a nitrogen stream at 400 ° C. and then in an ammonia gas atmosphere at 1000 ° C. in the same manner as in Example 1 to obtain an unoriented boron nitride having a diameter of about 15 m. Fiber was obtained.
- This unoriented boron nitride fiber was subjected to an orientation treatment in the same manner as in Example 3. At this time, the stretching ratio was 20.2%, the degree of orientation of the obtained boron nitride fiber was 0.82, and the tensile strength was 191 OMPa.
- the two cold fingers were filled with dry ice iacetone, and while stirring with a stirrer, 60 g of boron trichloride was condensed and dropped from the cold fingers directly attached to the three-necked flask over 2 hours. This produced a white boron trichloride-acrylonitrile adduct.
- the cold finger directly attached to the three-necked flask was removed, and 21.5 g of ammonium chloride dried at 110 ° C overnight was added.
- the suspension was heated to 125 ° C for 8 hours, producing almost no hydrogen chloride and a brown precipitate formed.
- the resulting precipitate was separated by filtration, washed with 100 ml of benzene, and dried under reduced pressure to obtain 24 g (77% yield) of a boron nitride precursor.
- the spun boron nitride precursor fiber was subjected to a heat treatment at 400 ° C. in a nitrogen gas stream and then at 1000 ° C. in an ammonia gas atmosphere, as in Example 1.
- An unoriented boron nitride fiber having a diameter of about 15 // m was obtained.
- This unoriented boron nitride fiber was subjected to an orientation treatment in the same manner as in Example 3. At this time, the draw ratio was 20.1%, the degree of orientation of the obtained boron nitride fiber was 0.81, and the tensile strength was 189 OMPa.
- the spun boron nitride precursor fiber was heated from room temperature to 400 ° C at a heating rate of l ° CZmin in a nitrogen stream, and after reaching 400 ° C, was allowed to cool to room temperature and was subjected to a heat treatment. . Then, in an ammonia gas atmosphere, the temperature is raised from room temperature to 1000 ° C at a rate of 2 ° C / min, and after reaching 1000 ° C, it is cooled to 500 ° C at a cooling rate of 5 ° C / min, and then to room temperature. Heat treatment was performed after cooling. As a result, about 15 iim of unoriented boron nitride fiber was directly obtained.
- This unoriented boron nitride fiber was subjected to an orientation treatment in the same manner as in Example 3. At this time, the draw ratio was 20.2%, the degree of orientation of the obtained boron nitride fiber was 0.82, and the tensile strength was 190 OMPa.
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Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP95912476A EP0699785B1 (en) | 1994-03-22 | 1995-03-20 | Boron nitride fiber and process for producing the same |
DE69503722T DE69503722T2 (de) | 1994-03-22 | 1995-03-20 | Boronitridfaser und verfahren zu deren herstellung |
US08/556,985 US5780154A (en) | 1994-03-22 | 1995-03-20 | Boron nitride fiber and process for production thereof |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5077994 | 1994-03-22 | ||
JP6/50779 | 1994-03-22 |
Publications (1)
Publication Number | Publication Date |
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WO1995025834A1 true WO1995025834A1 (fr) | 1995-09-28 |
Family
ID=12868322
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/JP1995/000500 WO1995025834A1 (fr) | 1994-03-22 | 1995-03-20 | Fibre de nitrure de bore et procede de production |
Country Status (4)
Country | Link |
---|---|
US (1) | US5780154A (ja) |
EP (1) | EP0699785B1 (ja) |
DE (1) | DE69503722T2 (ja) |
WO (1) | WO1995025834A1 (ja) |
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- 1995-03-20 DE DE69503722T patent/DE69503722T2/de not_active Expired - Fee Related
- 1995-03-20 WO PCT/JP1995/000500 patent/WO1995025834A1/ja active IP Right Grant
- 1995-03-20 US US08/556,985 patent/US5780154A/en not_active Expired - Fee Related
- 1995-03-20 EP EP95912476A patent/EP0699785B1/en not_active Expired - Lifetime
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JPH01290510A (ja) * | 1988-05-19 | 1989-11-22 | Mitsubishi Kasei Corp | ボラジン縮合体焼成物およびその製造方法 |
JPH0274614A (ja) * | 1988-09-07 | 1990-03-14 | Asahi Chem Ind Co Ltd | 窒化ホウ素繊維の製造法 |
JPH04272231A (ja) * | 1991-02-25 | 1992-09-29 | Toray Ind Inc | 黒鉛化繊維の製造方法 |
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Also Published As
Publication number | Publication date |
---|---|
DE69503722D1 (de) | 1998-09-03 |
EP0699785A1 (en) | 1996-03-06 |
EP0699785B1 (en) | 1998-07-29 |
US5780154A (en) | 1998-07-14 |
DE69503722T2 (de) | 1999-04-15 |
EP0699785A4 (en) | 1996-12-18 |
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