JP2011241142A - Method for producing graphite film - Google Patents

Abstract

PROBLEM TO BE SOLVED: To obtain a graphite film without (1) breakage when heated, (2) having high flatness, (3) superior electrical conductivity, and superior heat conductivity (4).SOLUTION: A method for producing a graphite film includes graphiting a raw material film. The raw material film is graphited through applying and holding it along the inner surface of a carbonaceous container. Preferably, the raw material film is graphited while applying current.

Description

  The present invention relates to a method for producing a graphite film used as a heat dissipation film.

  As a method for obtaining a graphite film having a large area of electrical conductivity and excellent thermal conductivity, polyphenylene oxadiazole, polybenzothiazole, polybenzobisthiazole, polybenzoxazole, polybenzobisoxazole, polythiazole, aromatic polyamide, A method for producing a graphite film (Patent Document 1) is known in which a polymer film such as aromatic polyimide is wound around cylindrical carbon and heated in an inert gas or in vacuum at 1800 ° C. or higher.

  In the example of (Patent Document 1), a polymer film having a length of 200 mm and a thickness of 50 μm is wrapped around a graphite cylinder having an outer diameter of 68 mm and heat-treated to produce a large-area graphite film.

  When heat-treating a polymer film longer than 10 m using a conventional method, it is necessary to increase the number of windings. However, when the number of windings is increased, there is a large difference in the heat history between the vicinity of the surface where the film is wound and the inside, and the physical properties may be lowered. In addition, since the heat history applied to the film was different, there was a difference in the amount of shrinkage, and the film was damaged during the heat treatment process, and wrinkles were easily formed. Furthermore, since it is wound around cylindrical graphitic carbon, thermal shrinkage during heating is restricted, and it may break during heating.

  In addition, when a conventional method is used, since the heat treatment is performed in a cylindrical shape, it is produced in a cylindrical shape. Therefore, in order to make the film flat, an operation such as rolling is required, and further, scratches are easily generated in the process.

  Further, as the thickness of the polymer film was increased to 75 μm or more, the difference in the thermal history in the film was increased, and it was easy to break during heating, and the cylindrical history was also likely to remain.

Japanese Patent Publication No. 7-88207

  Problems to be solved by the present invention are as follows: (1) No damage during heating, (2) High flatness, (3) Excellent electrical conductivity and thermal conductivity, (4) Long graphite To get a film.

  The present invention includes the following aspects.

  (1) A method for producing a graphite film in which a raw material film made of a polymer film and / or a carbonized polymer film is graphitized, and the raw material film is attached to the inner surface of a carbonaceous container and graphitized. And a method for producing a graphite film.

  (2) A method for producing a graphite film as described in (1) above, comprising a step of graphitizing while applying voltage and applying current.

  (3) The method for producing a graphite film as described in (1) or (2) above, wherein the energization is performed in the presence of carbon powder around the container. .

  (4) The method for producing a graphite film according to any one of (1) to (3), wherein the container is cylindrical.

  (5) The method for producing a graphite film according to any one of (1) to (4), wherein the container is a cylindrical container having an inner diameter of 200 mm or more.

  (6) The polymer film is polyimide, polyamide, polyoxadiazole, polybenzothiazole, polybenzobisthiazole, polybenzoxazole, polybenzobisoxazole, polyparaphenylene vinylene, polybenzimidazole, polybenzobisimidazole, The method for producing a graphite film according to any one of (1) to (5), comprising at least one polymer selected from polythiazole.

  (7) The method for producing a graphite film according to (6), wherein the polymer film is a polyimide film having a birefringence of 0.08 or more.

  (8) The method for producing a graphite film according to (6), wherein the polymer film is a polyimide film having a birefringence of 0.12 or more.

  (9) The polymer film is a polyimide film prepared by imidizing polymellitic acid containing pyromellitic dianhydride and p-phenylenediamine using a dehydrating agent and an imidization accelerator, (6 )-(8) The manufacturing method of the graphite film in any one of.

  (10) The polymer film uses a diamine and an acid dianhydride to synthesize a prepolymer having the acid dianhydride at both ends, and reacts the prepolymer with a diamine different from the above to synthesize a polyamic acid. The manufacturing method of the graphite film in any one of (6)-(8) which is a polyimide film produced by imidating the said polyamic acid.

  (11) The method for producing a graphite film according to any one of (6) to (10), wherein the polymer film is a polymer film having a length of 15 m or more.

  (12) The method for producing a graphite film according to any one of (6) to (10), wherein the polymer film is a polymer film having a length of 15 m or more and a width of 250 mm or more.

  (1) In the conventional method of winding around a small cylindrical graphite carbon having a diameter of less than 120 mm, the diameter is too small and the film is easily damaged during the heat treatment. In addition, when the cylindrical diameter is small, the number of windings increases. In addition, only a graphite having a cylindrical history easily remaining and inferior flatness was obtained. However, by enlarging the diameter of the cylinder of the present invention, it was possible to obtain a long graphite film with high flatness by reducing the number of times of winding and winding without breaking.

  Furthermore, by increasing the diameter, the difference in thermal history applied to the container and the cylindrical graphitic carbon may increase, but by combining with the current heating method, the uniformity of the thermal history is increased and the quality is excellent. A graphite film could be obtained.

  (2) In the case of heat-treating a polymer film having a length of 10 m or more in a conventional method in which a raw material film is wrapped and held around a carbonaceous core and heat-treated in an inert atmosphere or under reduced pressure, It is necessary to increase the number of windings over 10 laps. However, when the number of windings is increased, there is a large difference in the heat history between the vicinity of the surface where the film is wound and the inside, and the physical properties may be lowered. In addition, since the heat history applied to the film was different, there was a difference in the amount of shrinkage, and the film was damaged during the heat treatment process, and wrinkles were easily formed. Furthermore, since it is wound around cylindrical graphitic carbon, thermal shrinkage during heating is restricted, and it may break during heating. However, in the method of the present invention, the raw material film is wound around and held in a container that can be energized, and the container and the raw material are energized and heated. With the addition of a history, deformation such as shrinkage and expansion during heating occurred more uniformly than before, and a long graphite film excellent in electrical conductivity and thermal conductivity could be obtained without breakage.

  (3) Furthermore, conventionally, since heat treatment was performed by wrapping around a small cylindrical graphitic carbon having a diameter of less than 120 mm, shrinkage during heating was suppressed, and there was a case where breakage occurred. However, in the present invention, by attaching to the inner surface of the cylinder, the shrinkage is not restricted and a long graphite film can be obtained without being damaged.

Polyimide film and wedge-shaped sheet. The perspective view of a wedge-shaped sheet | seat.

  (1) A first method for producing a graphite film of the present invention is a method for producing a graphite film in which a raw material film comprising a polymer film and / or a carbonized polymer film is graphitized, and has an outer diameter of 120 mm or more. A method for producing a graphite film, characterized by being wound around a carbonaceous core and graphitized. More preferably, the graphitization is a step of graphitizing while applying voltage and applying current.

  (2) A second method for producing a graphite film of the present invention is a method for producing a graphite film in which a raw material film made of a polymer film and / or a carbonized polymer film is graphitized, and in a container that can be energized. A method for producing a graphite film, comprising the steps of: wrapping and holding a raw material film around a carbonaceous core, and applying a voltage to the container and graphitizing while energizing.

  (3) A third method for producing a graphite film of the present invention is a method for producing a graphite film in which a raw material film made of a polymer film and / or a carbonized polymer film is graphitized, and is an inner surface of a carbonaceous container. A method for producing a graphite film, characterized in that a raw material film is held together and graphitized. More preferably, the graphitization is a step of graphitizing while applying voltage and applying current.

<Graphite film>
Since the graphite film produced by the production method of the present invention has high thermal conductivity, for example, electronic devices such as servers, server personal computers, desktop personal computers, notebook personal computers, electronic dictionaries, PDAs, mobile phones, PDPs, It is suitable as a heat dissipation material for portable electronic devices such as portable music players.

<Raw film>
The raw material film that can be used in the present invention is a polymer film or a carbonized polymer film.

<Polymer film>
The polymer film that can be used in the present invention is not particularly limited, but is polyimide (PI), polyamide (PA), polyoxadiazole (POD), polybenzothiazole (PBT), polybenzobisthiazole (PBBT). ), Polybenzoxazole (PBO), polybenzobisoxazole (PBBO), polyparaphenylene vinylene (PPV), polyphenylene benzimidazole (PBI), polyphenylene benzobisimidazole (PPBI), and polythiazole (PT). Of these, a heat-resistant aromatic polymer film containing at least one selected from the above is preferable because the electrical conductivity and thermal conductivity of the finally obtained graphite are increased. What is necessary is just to manufacture these films with a well-known manufacturing method. Among these, polyimide is preferable because various materials and structures can be obtained by selecting various raw material monomers.

<Carbonized polymer film>
The carbonized polymer film used in the present invention is obtained by preheating a polymer film as a starting material under reduced pressure or in an inert gas. This preheating is usually performed at a temperature of about 1000 ° C., and for example, when the temperature is raised at a rate of 10 ° C./min, it is desirable to hold the temperature for about 30 minutes in the temperature range of 1000 ° C.

<Method of holding raw material film of the present invention in carbonaceous core and carbonaceous container>
Examples of the method of holding the raw material film of the present invention include (1) a method of winding the raw material film around a carbonaceous core, and (2) a method of attaching to the inner surface of the carbonaceous container.

  (1) In the method of winding the raw material film around the carbonaceous core, the carbonaceous core is preferably cylindrical, and the carbonaceous core has an outer diameter of 120 mm or more, preferably 150 mm or more, more preferably 200 mm or more, and still more preferably. It is 250 mm or more. When the carbonaceous core has a square shape, when the raw material film is wound, the film may be broken, but when the carbonaceous core is cylindrical, the raw material film is wound. In this case, it is preferable because the film is not easily broken and is not easily damaged. Further, in the conventional method of winding around a small cylindrical graphite carbon having a diameter of less than 120 mm, the diameter is too small and the film may be damaged during the heat treatment. In addition, when a long graphite film is obtained when the cylindrical diameter is small, it is necessary to increase the number of windings to 10 or more rounds, and the thermal history applied to the raw material film may vary, resulting in a decrease in physical properties. In addition, only a graphite having a cylindrical history easily remaining and inferior flatness was obtained. However, by increasing the diameter of the cylinder, it was difficult to break, the number of windings was reduced, and a long graphite film with high flatness could be obtained. However, when the carbonaceous core and the carbonaceous container are enlarged, the difference in the thermal history applied to the carbonaceous core and the carbonaceous container increases, for example, the difference in the thermal history between the end portion and the central portion of the core may increase. However, by combining with the electric heating method described later, the uniformity of the heat history is increased, and a graphite film having excellent quality can be obtained.

  That is, simply by increasing the size and diameter of the carbonaceous core and the carbonaceous container, the difference in the thermal history applied to the carbonaceous core and the carbonaceous container increases. For example, heat is generated at the end and center of the core. A new issue has arisen that the difference in history may increase. In the present invention, it has been found that a graphite having excellent quality can be obtained even with a carbonaceous core of 120 mm or more by conducting current heating. That is, when the core diameter is 120 mm or more, it has been difficult to make the heat treatment uniform, but as a result of intensive studies, even with a carbonaceous core having a diameter of 120 mm or more, a graphite having excellent quality can be obtained by conducting heating. It was found that it can be obtained.

  (2) In the method of attaching the raw material film to the inner surface of the carbonaceous container, the carbonaceous container is preferably cylindrical, and the carbonaceous container has an inner diameter of 200 mm or more, preferably 250 mm or more, more preferably 300 mm or more. In the conventional method of wrapping around a small cylindrical graphitic carbon having a diameter of less than 120 mm and performing heat treatment, shrinkage during heating is suppressed, and there is a case where breakage occurs. On the other hand, in the present invention, by attaching to the inner surface of the cylinder, the shrinkage is not restricted and a long graphite film can be obtained without breakage.

  As described above, by increasing the outer diameter of the carbonaceous core and the inner diameter of the carbonaceous container, it becomes possible to perform heat treatment with a large curvature radius of the graphite film, and graphitization tends to proceed smoothly on a flat surface. It becomes easy to obtain a graphite film excellent in thermal diffusivity. Further, the number of windings can be reduced, and the graphitization tends to proceed uniformly on the surface and inside, so that a graphite film having an excellent thermal diffusivity can be easily obtained.

<Method for Graphitizing Under Inert Gas Atmosphere / Depressurized Pressure of the Present Invention>
The graphitization of the present invention may be performed after the carbonized polymer film is once taken out and then transferred to a graphitization furnace, or may be continuously performed from carbonization. Graphitization is performed under reduced pressure or in an inert gas, and argon and helium are suitable as the inert gas. The heat treatment temperature needs to be 2000 ° C. or higher at a minimum, and finally heat treatment at 2400 ° C. or higher, more preferably 2600 ° C. or higher, more preferably 2800 ° C. or higher, in order to obtain graphite having excellent thermal conductivity. Good for.

  The higher the heat treatment temperature is, the higher the quality can be converted to graphite, but from the viewpoint of economy, it is preferable that the conversion to high quality graphite is possible at the lowest possible temperature. In order to obtain an ultra-high temperature of 2500 ° C. or higher, heating is usually performed by passing a current directly through the graphite heater and utilizing its juule heat. The consumption of the graphite heater proceeds at 2700 ° C. or more, and the consumption rate becomes about 10 times at 2800 ° C., and further about 10 times at 2900 ° C. Therefore, by improving the raw material polymer film, lowering the temperature at which conversion to high-quality graphite can be performed, for example, from 2800 ° C. to 2700 ° C. has a great economic effect. In a generally available industrial furnace, the maximum heat-treatable temperature is 3000 ° C.

<Method for Graphitizing While Energizing the Present Invention>
The graphitization method of the present invention is a method in which a raw material film made of a polymer film and / or a carbonized polymer film is held in a “container that can be directly energized by applying a voltage” described later, and the energization is possible. It includes a step of energizing a non-container and a raw material film by a method to be described later to graphitize.

  The first method of the present invention can be roughly classified into the following three types depending on the raw material film.

In the “container that can be energized directly by applying voltage” described later,
(Part 1) Hold a “carbonized polymer film” or
(Part 2) After obtaining a “carbonized polymer film” by preheating the “polymer film”, holding the “carbonized polymer film”, or
(Part 3) Hold the “polymer film” as an insulator,
The method includes a step of graphitizing while applying a voltage to the vessel and energizing the vessel.

  Hereinafter, (Part 1) to (Part 3) will be specifically described.

  (Part 1) When a carbonized polymer film is used as a raw material, the film is held in a container that can be directly energized by applying a voltage, and the film is graphitized by energizing by applying a voltage to the container. Is heated by two means by direct heat conduction from the exothermic container (1) and self-heating of the film (2), and becomes a graphite film with excellent quality. The details are as follows.

  In the conventional ordinary atmosphere and heat treatment under reduced pressure, the heating is performed by the heat conduction of the atmosphere gas and / or the radiant heat from the heater. Therefore, the means for heating the film is basically from the film surface to the inside. It is only one of the heat conductions.

  However, in the method of the present invention, the portion where the carbonized polymer film is in contact with the conductor (the container (may be a graphite container) and / or carbon powder) is on one surface and the other surface of the film. For this reason, Joule heat generated by voltage application is immediately transferred from both one surface and the other surface of the carbonized polymer film. As a result, carbonization proceeds from both one surface and the other surface. The film is heated by two means by direct heat conduction from the exothermic container and self-heating of the film, which will be described later, sufficiently heated to the inside of the film, and uniformly heat-treated in the surface layer and inside of the film.

  In the present invention, when a voltage is applied and a container that can be directly energized is energized, heat is generated by energization.

  In addition, when a carbonized polymer film is used as a starting material, when a voltage is applied to the container, a current flows in accordance with the change in electrical resistance according to the progress of carbonization because the film is already carbonized. As the graphitization proceeds, the resistance decreases, so that more current flows and the film itself generates heat. In particular, since current flows in both the surface layer and the inside, heat generation proceeds simultaneously in both the surface layer and the inside. As a result, uniform graphitization occurs.

  Furthermore, the current flows in accordance with the change in electrical resistance according to the progress of carbonization, and as the graphitization progresses, the resistance decreases, so the amount of current flowing through the film increases and the amount of heat generated by the film increases. , Graphitization easily proceeds. In particular, even if the heat generation is partially increased, the film itself generates heat and the thermal conductivity increases as the graphitization proceeds, so that heat is transmitted to the entire film and the film is uniformly heated.

  The carbonized polymer film before becoming graphite tends to be inferior in thermal conductivity as compared with graphite. Therefore, in conventional heat treatment under normal atmosphere and reduced pressure, the heating means is only one of heat conduction, so heat is not easily transmitted to the inside, and there is a difference in the state of graphitization between the surface layer and inside. It tends to graphitize only the surface layer and leave an insufficiently graphitized portion inside. As a result, in the conventional method, when the heat treatment was performed at a high temperature, an insufficient portion inside was foamed and burst, and the film became tattered.

  On the other hand, in the method of the present invention, the container itself that can be directly energized by applying a voltage generates heat as the voltage is applied, and at the same time, according to the change in electrical resistance according to the progress of carbonization / graphitization, A current flows through the carbonized part of the polymerized film, and the film itself generates heat. Therefore, it is possible to supply sufficient heat to the film by two means by direct heat conduction from the heated container and self-heating of the film, and sufficient heat is supplied even to the portion having poor internal heat conductivity, and the surface layer The graphitization proceeds simultaneously in the surface layer and inside without being graphitized only.

  In addition, since the electric conductivity is uniformly increased in the film plane, local electric field concentration does not occur in the film, local heat generation does not occur, and as a result, uniform graphitization proceeds on the surface and inside. . In addition, since the graphite after the heat treatment is very excellent in crystallinity and excellent in heat resistance, even if the electric field is concentrated and local heating occurs, the graphite becomes high quality without being damaged.

  (Part 2) Also, when an insulating polymer film is used as a raw material film, a carbonized polymer film obtained by preheating the film in an inert gas atmosphere and / or under reduced pressure is used. it can. The polymer film carbonized in this way can be graphitized by the method described above in (Part 1).

  (Part 3) Further, when an insulating polymer film is used as a raw material film, carbonization is likely to occur uniformly because it is energized from the beginning of the carbonization process up to graphite. Further, even in the case of an insulating polymer film, according to the manufacturing method of the present invention, the portion where the insulating polymer film is in contact with the conductor (graphite container and / or carbon powder) is the film. Since it is one surface and the other surface, Joule heat generated by voltage application is immediately transferred from both one surface and the other surface of the insulating polymer film. Therefore, carbonization proceeds from both one surface and the other surface.

  Thus, in the present invention, even in the case of an insulating polymer film, the conductor is in contact with both surfaces. As carbonization progresses, current continues to flow inside the film in response to changes in electrical resistance in accordance with the progress of carbonization inside the film, and the amount of current flowing through the film increases with the progress of carbonization. Since uniform heat generation occurs on the surface and inside, uniform graphitization easily proceeds. In addition, since the electric conductivity is increased uniformly in the film plane, local electric field concentration does not occur in the film, and local heat generation does not occur. As a result, uniform graphitization proceeds on the surface and inside. Moreover, since the crystallinity of the graphite after the heat treatment is very excellent and the heat resistance is excellent, even if the electric field is concentrated and local heating occurs, the graphite becomes high quality without being damaged.

  Furthermore, when the carbonaceous core and the carbonaceous container are enlarged, the difference in the thermal history applied to the carbonaceous core and the carbonaceous container increases, for example, the difference in the thermal history between the end portion and the central portion of the core may increase. However, when combined with the electric heating method, the uniformity of the thermal history is increased, and a graphite film having excellent quality can be obtained.

  The reason why the graphite film according to the present invention exhibits higher uniformity than the graphite film produced by the conventional production method and the mechanism can be estimated as described above, although further academic detailed research is necessary.

  <Energization method / state in which carbon powder is filled between a graphite container and a raw material film and / or around the outside of the graphite container>.

  The graphitization process of the raw material film of the present invention, particularly the energization method will be described.

  In the present invention, a method of applying a voltage by applying a voltage means applying an AC voltage and / or a DC voltage and applying a current.

  The raw material film graphitization process of the present invention is carried out by including a step of holding the raw material film in a container that can be directly energized by applying a voltage, and graphitizing while energizing the container by applying a voltage to the container. . For example, it is preferable to energize by the following methods (1) to (4). Here, the case of a graphite container will be described in particular, but the present invention is not necessarily limited to the graphite container.

  (1) A method in which a raw material film is held in a graphite container, and a voltage is applied to the graphite container itself to energize it.

  (2) A method of holding a raw material film in a graphite container, covering (filling) the outer periphery of the graphite container with carbon powder, and applying a voltage to the graphite container itself through the carbon powder to energize it. .

  (3) Hold the raw material film covered with carbon powder in the graphite vessel (hold the carbon powder between the graphite vessel and the raw material film), and the graphite vessel itself A method of applying a voltage to the energization.

  (4) Holding a raw material film covered with carbon powder in a graphite vessel (holding the carbon powder between the graphite vessel and the raw material film), and further, the graphite vessel Is covered with carbon powder (in the state where the outside of the graphite container is filled with carbon powder), and a voltage is applied to the graphite container itself through the carbon powder to energize it.

  Considering from the electrical conductivity of the container that can be directly energized and the manufactured film, depending on the size of the sample, as a result of energization, for example, a current of 10 mA or more flows through the raw material film, and the container and / Or the film generates heat. In particular, even when the initial insulator is converted to a conductor from the middle, a high-quality graphite film can be stably produced by preventing a sudden temperature rise by controlling the input power.

  In the step of holding the raw material film in a container which can be directly energized by applying a voltage according to the present invention and graphitizing while energizing the container by applying a voltage to the container, as a result, a voltage is applied to the raw material film and energized. The heating of the raw material film itself contributes. Accordingly, the film is uniformly heated on the inside and the surface of the film, and is also heated sufficiently uniformly from the periphery of the film, so that it is possible to obtain a graphite film that is more excellent in electric conductivity and heat conductivity than before. Furthermore, even when using a raw material film with a thickness of about 125 μm or about 225 μm, the film is heated uniformly from the inside, the surface, and the periphery of the film. A disturbing graphite layer is not formed, the internal decomposition gas is easily released, and the film is not damaged by the decomposition gas, and a thick graphite film excellent in electrical conductivity and thermal conductivity can be obtained.

  The energization method (2), in which a raw material film is held in a graphite container, the outer periphery of the graphite container is covered with carbon powder, and a voltage is applied to the graphite container itself through the carbon powder to energize it. The method is superior to the current conduction method (1) in which the raw material film is held in a graphite container and a voltage is applied to the graphite container itself to conduct electricity and the characteristics are not varied. It is excellent in obtaining a graphite film. This is because the graphite container and / or the raw material film are uniformly energized and heated by covering the graphite container with carbon powder.

  Furthermore, as in the energization methods (3) and (4), holding the raw material film covered with the carbon powder in the graphite vessel also means that the energization and heating applied to the graphite vessel and / or the raw material film is uniform. It is preferable to become.

  The heat treatment temperature given from the heat generated as a result of energization and given to the raw material film should be at least 2400 ° C., preferably 2600 ° C. or more, and finally heat treatment at a temperature of 2700 ° C. or more. It is more preferable to perform heat treatment at 2800 ° C. or higher.

  In the present invention, by holding the container holding the raw material film in another container, the voltage and / or heat applied to the container can be made uniform, and there is a difference in the quality of the graphite produced between the containers. It does not occur. Furthermore, the density of the carbon powder around the outside of the container holding the raw film can be made uniform (filling density when filling), and even when a large number of the containers are used, they are produced between the containers. The quality of the graphite produced is characterized by no difference.

  In addition, the temperature described in the present invention can be measured using a radiation thermometer or the like, for example, on the outer wall or a part of the inside of a container that can be directly energized.

<Container that can be energized by applying voltage>
The container that can be directly energized by applying a voltage according to the present invention is, for example, a container made of tungsten, molybdenum, or graphite. In applications such as the present invention where heating is performed by energization to a temperature range of 2500 ° C., considering the ease of handling, industrial availability, etc., the container used is a graphite container. Is particularly preferred. The term “graphite” as used herein is a broad concept including materials that mainly contain graphite as long as it can be heated to the above temperature range, and examples thereof include isotropic graphite and extruded graphite. Isotropic graphite having excellent electrical and thermal conductivity and excellent homogeneity is preferable when an electric current is applied and repeatedly used.

<Carbon powder>
The carbon powder used in the present invention is heated (by energization) to a temperature range of 2500 ° C. as in the present invention.

The carbon powder here is a broad concept that is not particularly limited as long as it is a powder mainly containing carbon. For example, a substance mainly containing an organic substance, powder, or fiber may be heat treated and then pulverized into a powder or granulated. The temperature of the heat treatment is 200 ° C. or higher, preferably 500 ° C. or higher, more preferably 1000 ° C. or higher or 1500 ° C. or higher. Further, a substance mainly containing carbon such as natural pitch and / or artificial pitch, coke and carbon black may be used. The carbon powder may be graphite. As used herein, as long as it can be heated to the above temperature range, it is a broad concept including materials that mainly contain graphite. For example, a crushed graphite cloth, isotropic graphite The thing which grind | pulverized, the thing which grind | pulverized extruded graphite, etc. are mentioned. The powder shape, particle size, particle size distribution, etc. of the carbon powder are not particularly limited. <Polyimide film>
Polyimide film is more prone to carbonization and graphitization of film than raw materials made from other organic materials, so the electrical conductivity of the film is likely to increase uniformly at low temperatures, and the electrical conductivity itself increases. Cheap. As a result, when the raw material film is held in a container that can be directly energized by applying a voltage and graphitized while energizing by applying a voltage to the container, the film portion is uniform as the carbonization progresses. Current flows through the surface, and uniform heat generation occurs on the surface and inside, resulting in graphite having high thermal conductivity even when the thickness is small. In addition, since the resulting graphite has excellent crystallinity and excellent heat resistance, even if the electric field is concentrated and local heating occurs, the graphite does not break and becomes high quality graphite.

<Polyimide film and birefringence>
In the polyimide film used in the present invention, the birefringence Δn related to the in-plane orientation of the molecule is 0.08 or more, preferably 0.10 or more, more preferably 0.12 or more in any direction in the film plane. Most preferably, it is 0.14 or more.

<Raw film and birefringence>
The higher the birefringence, the more easily the carbonization (carbonization) and graphitization of the film proceeds, and the electrical conductivity of the film tends to increase. As a result, in the step of holding the raw material film in a container that can be directly energized by applying a voltage, and graphitizing while energizing the container by applying a voltage to the container, the film portion has an electric resistance corresponding to the progress of carbonization. As the carbonization progresses, the amount of current flowing through the film increases and uniform heat generation occurs on the surface and inside, so that uniform graphitization easily proceeds. In addition, since the electric conductivity is increased uniformly in the film plane, local electric field concentration does not occur in the film, and local heat generation does not occur. As a result, uniform graphitization proceeds on the surface and inside.

  In addition, since carbonization (carbonization) and graphitization proceed at a low temperature, the electrical conductivity of the film increases during the low-temperature heat treatment, uniform heat generation occurs on the surface and inside, and uniform graphitization proceeds. It becomes easy.

  In addition, the higher the birefringence, the better the crystallinity and the heat resistance. Therefore, even if the electric field is concentrated and local heating occurs, the graphite film does not break and becomes a high quality graphite film.

  Further, even when the thickness of the raw material is increased, graphitization is uniformly progressed on the surface and inside, so that graphite having excellent thermal conductivity can be obtained.

  Moreover, the higher the birefringence, the more significantly the thermal conductivity of the resulting graphite film. Therefore, the maximum processing temperature given from the heat generated as a result of energization and given to the raw material film can be lowered, and the power consumption can be reduced. A high quality graphite film can be obtained even with a short heat treatment.

  The reason why graphitization is likely to occur when birefringence is high is not clear, but it is necessary to rearrange the molecules for graphitization, and polyimide films with high birefringence and excellent molecular orientation have minimal molecular rearrangement. Therefore, among polyimide films, a polyimide film with better orientation is the highest processing temperature associated with heat generation due to a relatively low-temperature energization process, and a highly crystalline graphite film even if it is thick. It is estimated that

<Birefringence>
Birefringence here means the difference between the refractive index in an arbitrary direction in the film plane and the refractive index in the thickness direction, and the birefringence Δnx in the arbitrary direction X in the film plane is given by the following formula (Formula 1). It is done.

  1 and 2, a specific method for measuring birefringence is illustrated. In the plan view of FIG. 1, a thin wedge-shaped sheet 2 is cut out from the film 1 as a measurement sample. The wedge-shaped sheet 2 has an elongated trapezoidal shape having one oblique side, and its base angle is a right angle. At this time, the base of the trapezoid is cut out in a direction parallel to the X direction. FIG. 2 is a perspective view of the measurement sample 2 cut out in this way. When sodium light 4 is irradiated at right angles to the cut-out cross section corresponding to the bottom side of the trapezoidal sample 2 and observed with a polarizing microscope from the cut-out cross section side corresponding to the oblique side of the trapezoidal sample 2, the interference fringes 5 are observed. If the number of interference fringes is n, the birefringence Δnx in the film in-plane X direction is expressed by the following formula (Formula 2).

  Here, λ is the wavelength 589 nm of the sodium D line, and d is the width 3 of the sample corresponding to the trapezoidal height of the sample 2.

  The above-mentioned “arbitrary direction X in the film plane” means, for example, the X direction is the 0 ° direction, 45 ° direction, 90 ° direction, 135 ° direction in the plane with reference to the direction of material flow during film formation. In any direction.

<Thermal properties, mechanical properties, physical properties, and chemical properties of polyimide films>
Moreover, the polyimide film used as the raw material for graphite used in the present invention preferably has an average linear expansion coefficient of less than 2.5 × 10 ⁻⁵ / ° C. in the range of 100 to 200 ° C. If the linear expansion coefficient is less than 2.5 × 10 ⁻⁵ / ° C., the elongation during the heat treatment is small, the graphitization proceeds smoothly, and the graphite is not brittle and has excellent various properties. By using such a polyimide film as a raw material, the conversion to graphite starts at 2400 ° C., and the conversion can occur in graphite having sufficiently high crystallinity at 2700 ° C. The linear expansion coefficient is more preferably 2.0 × 10 ⁻⁵ / ° C. or less.

  Note that the linear expansion coefficient of the raw material film was determined by first heating the sample to 350 ° C. at a temperature rising rate of 10 ° C./min using TMA (thermomechanical analyzer), and then air-cooling to room temperature and then 10 ° C. again. It is obtained by raising the temperature to 350 ° C. at a rate of temperature rise / min and measuring the average linear expansion coefficient at 100 ° C. to 200 ° C. during the second temperature rise. Specifically, using a thermomechanical analyzer (TMA: Seiko Electronics SSC / 5200H; TMA120C), a 3 mm wide × 20 mm long film sample is set in a predetermined jig, and a load of 3 g is applied in a tensile mode. Is measured in a nitrogen atmosphere.

  Moreover, the polyimide film used for this invention is preferable from the ability to graphitize more easily if the elasticity modulus is 2.5 GPa or more. That is, if the elastic modulus is 2.5 GPa or more, the film can be prevented from being damaged by the shrinkage of the film during the heat treatment, and graphite excellent in various properties can be obtained.

  In addition, the elasticity modulus of a film can be measured based on ASTM-D-882. A more preferable elastic modulus of the polyimide film is 3.0 GPa or more, preferably 4.0 GPa or more, and more preferably 5.0 GPa or more. If the elastic modulus of the film is less than 2.5 GPa, the film tends to be damaged and deformed due to shrinkage of the film during heat treatment, and the resulting graphite has poor crystallinity and tends to have poor density and thermal conductivity.

  The water absorption rate of the film was measured as follows. In order to dry the film completely, it was dried at 100 ° C. for 30 minutes to prepare a sample having a 25 μm thickness and a 10 cm square. This weight is measured and designated as A1. A 25 μm-thick 10 cm square sample was immersed in distilled water at 23 ° C. for 24 hours, and the surface water was wiped away and the weight was immediately measured. This weight is A2. The water absorption was determined from the following formula.

Water absorption rate (%) = (A2−A1) ÷ A1 × 100
<Preparation method of polyimide film>
The polyimide film used in the present invention is prepared by mixing an organic solution of polyamic acid, which is a polyimide precursor, with an imidization accelerator, and then casting it on a support such as an endless belt or a stainless drum, followed by drying and baking. Can be produced by imidization.

  As a method for producing the polyamic acid used in the present invention, a known method can be used. Usually, at least one kind of aromatic dianhydride and at least one kind of diamine are substantially equimolar amounts in an organic solvent. Dissolved in. The obtained organic solution is stirred under controlled temperature conditions until the polymerization of the acid dianhydride and the diamine is completed, whereby a polyamic acid can be produced. Such a polyamic acid solution is usually obtained at a concentration of 5 to 35 wt%, preferably 10 to 30 wt%. When the concentration is in this range, an appropriate molecular weight and solution viscosity can be obtained.

  Any known method can be used as the polymerization method. For example, the following polymerization methods (1) to (5) are preferable.

  (1) A method in which an aromatic diamine is dissolved in an organic polar solvent, and this is reacted with a substantially equimolar aromatic tetracarboxylic dianhydride for polymerization.

  (2) An aromatic tetracarboxylic dianhydride is reacted with a small molar amount of an aromatic diamine compound in an organic polar solvent to obtain a prepolymer having acid anhydride groups at both ends. Then, the method of superposing | polymerizing using an aromatic diamine compound so that it may become substantially equimolar with respect to aromatic tetracarboxylic dianhydride.

  In this method, the prepolymer having the acid dianhydride at both ends is synthesized using the diamine and the acid dianhydride described in claim 11, and the polypolymer is synthesized by reacting the prepolymer with a diamine different from the above. It is the same as the method to do.

  (3) An aromatic tetracarboxylic dianhydride and an excess molar amount of the aromatic diamine compound are reacted in an organic polar solvent to obtain a prepolymer having amino groups at both ends. Subsequently, after adding an aromatic diamine compound to the prepolymer, polymerization was performed using the aromatic tetracarboxylic dianhydride so that the aromatic tetracarboxylic dianhydride and the aromatic diamine compound are substantially equimolar. how to.

  (4) After dissolving and / or dispersing aromatic tetracarboxylic dianhydride in an organic polar solvent, an aromatic diamine compound is used so as to be substantially equimolar with respect to the acid dianhydride. Polymerization method.

  (5) A method of polymerizing by reacting a substantially equimolar mixture of aromatic tetracarboxylic dianhydride and aromatic diamine in an organic polar solvent.

  Among these, a method of performing polymerization by performing sequential control (sequence control) (combination of block polymers / control of connection between block polymer molecules) via the prepolymer shown in (2) and (3) is preferable. By using this method, it is easy to obtain a polyimide film having a large birefringence and a small linear expansion coefficient. By heat-treating this polyimide film, the crystallinity is high, and the density and thermal conductivity are excellent. This is because it becomes easier to obtain graphite. Further, it is presumed that, when controlled regularly, the aromatic rings overlap, and graphitization is likely to proceed even at low temperature heat treatment. Also, increasing the imide group content to increase birefringence decreases the carbon ratio in the resin and decreases the carbonization yield after graphite treatment, but the polyimide film synthesized with sequential control is This is preferable because the birefringence can be increased without reducing the carbon ratio.

  Acid dianhydrides that can be used for the synthesis of polyimide in the present invention are pyromellitic dianhydride, 2,3,6,7-naphthalenetetracarboxylic dianhydride, 3,3 ′, 4,4′-biphenyl. Tetracarboxylic dianhydride, 1,2,5,6-naphthalene tetracarboxylic dianhydride, 2,2 ′, 3,3′-biphenyltetracarboxylic dianhydride, 3,3 ′, 4,4 ′ -Benzophenonetetracarboxylic dianhydride, 2,2-bis (3,4-dicarboxyphenyl) propane dianhydride, 3,4,9,10-perylenetetracarboxylic dianhydride, bis (3,4- Dicarboxyphenyl) propane dianhydride, 1,1-bis (2,3-dicarboxyphenyl) ethane dianhydride, 1,1-bis (3,4-dicarboxyphenyl) ethane dianhydride, bis (2 , 3-Zical Xylphenyl) methane dianhydride, bis (3,4-dicarboxyphenyl) ethane dianhydride, oxydiphthalic dianhydride, bis (3,4-dicarboxyphenyl) sulfone dianhydride, p-phenylenebis (trimerit Acid monoester acid anhydride), ethylene bis (trimellitic acid monoester acid anhydride), bisphenol A bis (trimellitic acid monoester acid anhydride), and the like, which may be used alone or in any It can be used in a mixture of proportions.

  Examples of the diamine that can be used in the synthesis of the polyimide in the present invention include 4,4′-oxydianiline, p-phenylenediamine, 4,4′-diaminodiphenylpropane, 4,4′-diaminodiphenylmethane, benzidine, 3,3. '-Dichlorobenzidine, 4,4'-diaminodiphenyl sulfide, 3,3'-diaminodiphenyl sulfone, 4,4'-diaminodiphenyl sulfone, 4,4'-diaminodiphenyl ether (4,4'-oxydianiline), 3,3'-diaminodiphenyl ether (3,3'-oxydianiline), 3,4'-diaminodiphenyl ether (3,4'-oxydianiline), 1,5-diaminonaphthalene, 4,4'-diaminodiphenyl Diethylsilane, 4,4'-diaminodiphenylsilane, 4,4 ' Diaminodiphenylethylphosphine oxide, 4,4′-diaminodiphenyl N-methylamine, 4,4′-diaminodiphenyl N-phenylamine, 1,4-diaminobenzene (p-phenylenediamine), 1,3-diaminobenzene, Including 1,2-diaminobenzene and the like, which can be used alone or in any proportion of the mixture.

  In particular, from the viewpoint of increasing the elastic modulus and increasing the birefringence by decreasing the linear expansion coefficient, the acid dianhydride represented by the following formula (1) is used as a raw material in the production of the polyimide film in the present invention. It is preferable.

Here, R ₁ is any one selected from the group of divalent organic groups included in the following formulas (2) to (14),

Here, each of R ₂ , R ₃ , R ₄ , and R ₅ can be any selected from the group of —CH ₃ , —Cl, —Br, —F, or —OCH ₃ .

  By using the above-mentioned acid dianhydride, a polyimide film having a relatively low water absorption can be obtained, which is also preferable from the viewpoint that foaming due to moisture can be prevented in the graphitization process.

In particular, when an organic group containing a benzene nucleus as shown in the formulas (2) to (14) is used as R ₁ in the acid dianhydride, the molecular orientation of the resulting polyimide film increases, This is preferable from the viewpoints of low expansion coefficient, high elastic modulus, high birefringence, and low water absorption.

  In order to further reduce the linear expansion coefficient, increase the elastic modulus, increase the birefringence, and decrease the water absorption, an acid dianhydride represented by the following formula (15) is used as a raw material for the synthesis of the polyimide in the present invention. That's fine.

In particular, a polyimide film obtained by using an acid dianhydride having a structure in which a benzene ring is linearly bonded by two or more ester bonds as a raw material has a very linear conformation as a whole although it contains a bent chain. It has a relatively rigid property. As a result, the linear expansion coefficient of the polyimide film can be reduced by using this raw material, for example, 1.5 × 10 ⁻⁵ / ° C. or less. Further, the elastic modulus can be increased to 5 GPa or more, and the water absorption can be decreased to 1.5% or less.

  In order to further reduce the linear expansion coefficient, increase the elastic modulus, and increase the birefringence, the polyimide in the present invention is preferably synthesized using p-phenylenediamine as a raw material.

  In the present invention, the most suitable diamines used for the synthesis of polyimide are 4,4′-oxydianiline and p-phenylenediamine, and the total moles of these alone or the two are 40% by mole based on the total diamines. More preferably, it is 50 mol% or more, more preferably 70 mol% or more, and even more preferably 80 mol% or more. Furthermore, it is preferable that p-phenylenediamine contains 10 mol% or more, further 20 mol% or more, further 30 mol% or more, and further 40 mol% or more. If the content of these diamines is less than the lower limit of these mol% ranges, the resulting polyimide film tends to have a high linear expansion coefficient, a low elastic modulus, and a low birefringence. However, if the total amount of diamine is p-phenylenediamine, it is difficult to obtain a thick polyimide film with less foaming, so 4,4'-oxydianiline is preferably used.

  In the present invention, the most suitable acid dianhydride used for the synthesis of the polyimide film is pyromellitic dianhydride and / or p-phenylenebis represented by the formula (15) (trimellitic acid monoester dianhydride). And the total mole of these alone or the two is 40 mole% or more, further 50 mole% or more, further 70 mole% or more, or even 80 mole% or more based on the total acid dianhydride. Is preferred. If the amount of these acid dianhydrides used is less than 40 mol%, the resulting polyimide film tends to have a large linear expansion coefficient, a small elastic modulus, and a small birefringence.

  Moreover, you may add additives, such as carbon black and a graphite, with respect to a polyimide film, a polyamic acid, and a polyimide resin.

  Preferred solvents for synthesizing the polyamic acid are amide solvents N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-2-pyrrolidone and the like, N, N-dimethylformamide, N, N-dimethylacetamide can be used particularly preferably.

  Next, a polyimide production method includes a heat curing method in which polyamic acid as a precursor is converted to imide by heating, or a polyhydric acid such as acetic anhydride and other dehydrating agents, picoline, quinoline, isoquinoline, Any of the chemical curing methods in which imide conversion is performed using a tertiary amine such as pyridine as an imidization accelerator may be used. Among them, a higher boiling point such as isoquinoline is preferable. This is preferable because it does not evaporate in the initial stage of film production, and the catalytic effect is easily exhibited until the last step of drying. In particular, the resulting film has a low coefficient of linear expansion, high modulus of elasticity, high birefringence, and can be rapidly graphitized at a relatively low temperature to obtain high-quality graphite. Cure is preferred. In particular, the combined use of a dehydrating agent and an imidization accelerator is preferable because the resulting film has a small linear expansion coefficient, a large elastic modulus, and a large birefringence. In addition, the chemical cure method is an industrially advantageous method that is excellent in productivity because the imidization reaction proceeds faster and the imidization reaction can be completed in a short time in the heat treatment.

  In the production of a film by a specific chemical cure, first, an imidization accelerator comprising a dehydrating agent and a catalyst of a stoichiometric amount or more is added to a polyamic acid solution, an organic film such as a support plate, PET, a drum, or an endless belt A film having self-supporting properties is obtained by casting or coating on a support such as a film to evaporate the organic solvent. Next, the self-supporting film is further heated and dried to be imidized to obtain a polyimide film. The temperature during the heating is preferably in the range of 150 ° C to 550 ° C. There is no particular limitation on the rate of temperature increase at the time of heating, but it is preferable to gradually heat in a continuous or stepwise manner so that the maximum temperature falls within the predetermined temperature range. Although the heating time varies depending on the film thickness and the maximum temperature, it is generally preferably in the range of 10 seconds to 10 minutes after reaching the maximum temperature. Furthermore, if the process of fixing or stretching the film to prevent shrinkage is included in the polyimide film manufacturing process, the resulting film has a low coefficient of linear expansion, a high elastic modulus, and a high birefringence. It is preferable because it tends to be easy.

<Graphitization of raw material film including polyimide film>
In the graphitization treatment, after carbonization by heat treatment, it is converted into a graphite structure, and in that case, the carbon-carbon bond must be cleaved and recombined. In order to make graphitization as easy as possible, its cleavage and recombination must occur with minimal energy. The molecular orientation of the starting material film (for example, the polymer film listed above, particularly the polyimide film) affects the arrangement of carbon atoms in the carbonized film, and the molecular orientation of the carbon-carbon bond during graphitization. It can have the effect of reducing the energy of cleavage and recombination. Therefore, graphitization at a relatively low temperature becomes possible by designing a molecule so that a high degree of molecular orientation is likely to occur. The effect of this molecular orientation becomes more prominent by adopting a two-dimensional molecular orientation parallel to the film surface.

  The second feature of the graphitization reaction is that if the raw material film is thick, the graphitization hardly proceeds at a low temperature. Therefore, when a thick raw material film is graphitized, a situation may occur in which a graphite structure is formed in the surface layer but is not yet formed into a graphite structure. The molecular orientation of the raw film promotes graphitization inside the film, and as a result, it can be converted into good quality graphite at a lower temperature.

  The fact that the graphitization proceeds almost simultaneously in the surface layer and inside of the raw film also helps to avoid the situation where the graphite structure formed in the surface layer is destroyed due to the gas generated from the inside. Enables graphitization of thick films. The raw material films produced in the present invention (for example, the polymer films listed above, particularly polyimide films) are considered to have the optimal molecular orientation for producing such an effect.

<Thickness, length, width of graphite film>
The specific level of the thickness of the graphite film produced by the production method of the present invention is 20 μm or more, preferably 50 μm or more, and more preferably 90 μm or more. In particular, when the thickness is 90 μm or more, the amount of heat transport increases, so that heat can be easily released from the heat generating device, and the temperature rise can be suppressed.

  The specific level of the length of the graphite film produced by the production method of the present invention is 10 m or more, preferably 20 m or more, more preferably 30 m or more. Moreover, the specific level of the width of the graphite film produced by the production method of the present invention is 200 mm or more, preferably 300 mm or more, and more preferably 400 mm or more. In this way, since a graphite film can be obtained in a large area, when using a graphite film as a heat dissipation material, cut various shapes of graphite film in various sizes, especially in accordance with the shape and mechanism of electronic equipment. In doing so, it is possible to increase the degree of freedom of the combination of cuts, and it is possible to reduce unnecessary portions generated in the cuts.

<Thermal diffusivity of graphite film>
The thermal diffusivity of the graphite film produced by the production method of the present invention is 7.0 × 10 ⁻⁴ m ² / S or more, preferably 7.5 × 10 ⁻⁴ m ² / S or more, more preferably 8. It is good that it is 0 × 10 ⁻⁴ m ² / S or more. When it is 7.0 × 10 ⁻⁴ m ² / S or more, the heat conductivity is high, so that heat is easily released from the heat generating device, and the temperature rise of the heat generating device can be suppressed. On the other hand, if it is less than 7.0 × 10 ⁻⁴ m ² / S, the heat conductivity is poor, so heat cannot be released from the heat generating device, and the temperature rise of the heat generating device cannot be suppressed.

As described above, a method for producing a graphite film for graphitizing the raw material film of the present invention,
(1) Wrapped around a carbonaceous core having an outer diameter of 120 mm or more, and graphitized. Preferably, the graphitization is performed while the graphitization is energized.
(2) A raw material film is wound around a carbonaceous core in a container that can be energized, and graphitized while energized.
(3) The raw material film is held on the inner surface of the carbonaceous container and graphitized. Preferably, the graphitization is performed while the graphitization is energized.
This makes it possible to obtain (1) a long graphite film without breakage during heating, (2) high flatness, (3) excellent electrical conductivity and thermal conductivity, and (4) a long graphite film.

<Applications>
Since the graphite film produced by the production method of the present invention has high thermal conductivity and electrical conductivity, for example, electronic devices such as servers, server personal computers, desktop personal computers, notebook personal computers, electronic dictionaries, PDAs, mobile phones , Portable electronic devices such as portable music players, liquid crystal displays, plasma displays, LEDs, organic EL, inorganic EL, liquid crystal projectors, display devices such as watches, ink jet printers (ink heads), electrophotographic devices (developing devices, fixing devices, Image forming apparatuses such as heat rollers and heat belts, semiconductor elements, semiconductor packages, semiconductor sealing cases, semiconductor die bonding, CPU, memory, power transistors, power transistor cases, and other semiconductor related parts, rigid wiring boards, flexible wiring boards ,ceramic Wiring boards such as wire boards, build-up wiring boards, and multilayer boards (the above-mentioned wiring board includes a printed wiring board), vacuum processing equipment, semiconductor manufacturing equipment, manufacturing equipment such as display equipment manufacturing equipment, and heat insulating materials , Heat insulation devices such as vacuum insulation materials and radiation insulation materials, DVD (optical pickup, laser generator, laser receiver), data recording equipment such as hard disk drives, cameras, video cameras, digital cameras, digital video cameras, microscopes, CCDs It is suitable as a heat radiating material, a heat radiating component, a cooling component, a temperature adjusting component, and an electromagnetic shielding component such as an image recording device such as a battery charger, a battery device such as a lithium ion battery and a fuel cell.

<Usage etc.>
Also, in use, resin on one side and / or both sides to improve heating element, heat sink, heat pipe, water cooling system, Peltier element, housing, hinge fixing, thermal diffusibility, heat dissipation, and handling A layer, a ceramic layer, a metal layer, an insulating layer, or a conductive layer may be formed.

  In the following, various examples of the present invention will be described together with some comparative examples, but the present invention is not limited to these examples.

  The present invention may include the following aspects.

  (1) The first is a method for producing a graphite film in which a raw material film comprising a polymer film and / or a carbonized polymer film is graphitized, and the raw material film is wound around a carbonaceous core having an outer diameter of 120 mm or more. A method for producing a graphite film, characterized by being graphitized.

  (2) The second is a method for producing a graphite film in which a raw material film made of a polymer film and / or a carbonized polymer film is graphitized, and the raw material film is placed on a carbonaceous core in an energizable container. A method for producing a graphite film, comprising the steps of: wrapping and holding, and applying a voltage to the container to graphitize while energizing.

  (3) The third is a method for producing a graphite film in which a raw material film made of a polymer film and / or a carbonized polymer film is graphitized, and the raw material film is held on the inner surface of the carbonaceous container. A method for producing a graphite film, characterized by being graphitized.

  (4) Fourth, the method for producing a graphite film according to any one of (1) and (3), comprising a step of graphitizing while applying a voltage and energizing the graphite film. Manufacturing method.

  (5) Fifth is the method for producing a graphite film according to any one of (1) to (4), wherein the energization is performed in a state where carbon powder is present around the container. A method for producing a graphite film, wherein

  (6) Sixth is the method for producing a graphite film according to any one of (1) to (5), wherein the container and / or the carbonaceous core is cylindrical.

  (7) Seventh is the method for producing a graphite film according to any one of (2) to (6), wherein the container is a cylindrical container having an inner diameter of 200 mm or more.

  (8) Eighth, the carbonaceous core is a carbonaceous core having an outer diameter of 150 mm or more, according to any one of (1), (2), and (4) to (7). It is a manufacturing method of a graphite film.

  (9) Ninth, the polymer film is made of polyimide, polyamide, polyoxadiazole, polybenzothiazole, polybenzobisthiazole, polybenzoxazole, polybenzobisoxazole, polyparaphenylene vinylene, polybenzimidazole, poly The method for producing a graphite film according to any one of (1) to (8), comprising at least one polymer selected from benzobisimidazole and polythiazole.

  (10) Tenth is the method for producing a graphite film according to (9), wherein the polymer film is a polyimide film having a birefringence of 0.08 or more.

  (11) The eleventh aspect is the method for producing a graphite film according to (9), wherein the polymer film is a polyimide film having a birefringence of 0.12 or more.

  (12) The twelfth aspect is a polyimide film in which the polyimide film is prepared by imidizing polymellitic acid containing pyromellitic dianhydride and p-phenylenediamine using a dehydrating agent and an imidization accelerator. It is the manufacturing method of the graphite film in any one of (9)-(11) characterized by the above-mentioned.

  (13) In the thirteenth, the polyimide film synthesizes a prepolymer having the acid dianhydride at both ends using a diamine and an acid dianhydride, and the prepolymer is reacted with a diamine different from the above to form a polyamic acid. The method for producing a graphite film according to any one of (9) to (11), which is a polyimide film produced by synthesizing and imidizing the polyamic acid.

  (14) The fourteenth aspect is the method for producing a graphite film according to any one of (9) to (13), wherein the polymer film is a polymer film having a length of 15 m or more.

  (15) The method for producing a graphite film according to any one of (9) to (13), wherein the polymer film is a polymer film having a length of 15 m and a width of 250 mm or more, It is.

  (16) Sixteenth is a graphite film produced by the production method according to any one of (1) to (15).

(17) The seventeenth is a graphite film manufactured by the manufacturing method according to any one of (1) to (16), wherein the film has a length of 10 m, a width of 200 mm or more, and heat in a plane direction. A graphite film having a diffusivity of 7.5 × 10 ⁻⁴ m ² / S or more.

(Preparation method of polyimide film A)
In a DMF (dimethylformamide) solution in which 1 equivalent of 4,4′-oxydianiline was dissolved, 1 equivalent of pyromellitic dianhydride was dissolved to obtain a polyamic acid solution (18.5 wt%).

  While this solution was cooled, an imidation catalyst containing 1 equivalent of acetic anhydride, 1 equivalent of isoquinoline, and DMF was added to the carboxylic acid group contained in the polyamic acid to degas. Next, this mixed solution was applied onto an aluminum foil so as to have a predetermined thickness after drying. The mixed solution layer on the aluminum foil was dried using a hot air oven and a far infrared heater.

  The drying conditions for film production when the finished thickness is 75 μm are shown. The mixed solution layer on the aluminum foil was dried in a hot air oven at 120 ° C. for 240 seconds to form a self-supporting gel film. The gel film was peeled off from the aluminum foil and fixed to the frame. Furthermore, the gel film is heated stepwise in a hot air oven at 120 ° C. for 30 seconds, 275 ° C. for 40 seconds, 400 ° C. for 43 seconds, 450 ° C. for 50 seconds, and a far infrared heater at 460 ° C. for 23 seconds. And dried.

As described above, a polyimide film having a thickness of 75 μm (polyimide film A: elastic modulus 3.1 GPa, water absorption 2.5%, birefringence 0.10, linear expansion coefficient 3.0 × 10 ⁻⁵ / ° C.) manufactured. In addition, when producing films with other thicknesses, the firing time was adjusted in proportion to the thickness. For example, in the case of a film having a thickness of 225 μm, the firing time was set to three times that in the case of 75 μm. Further, when the thickness is thick, it is necessary to take a sufficient baking time at a low temperature in order to prevent foaming due to evaporation of the solvent or imidization catalyst of the polyimide film.

  In actual graphitization, a polyimide film having a thickness of 75 μm and 125 μm made by Apical AH manufactured by Kaneka Corporation was used in the same manner as described above.

(Preparation method of polyimide film B)
After 4 equivalents of pyromellitic dianhydride was dissolved in a DMF solution in which 3 equivalents of 4,4′-oxydianiline was dissolved in polyamic acid, a prepolymer having acid anhydrides at both ends was synthesized. A polyimide film with a thickness of 75 μm (polyimide film C: elastic modulus 4.1 GPa) was used in the same manner as polyimide film A except that polyamic acid obtained by dissolving 1 equivalent of p-phenylenediamine in a solution containing a prepolymer was used. , Water absorption 2.1%, birefringence 0.14, linear expansion coefficient 1.6 × 10 ⁻⁵ / ° C.).

  In actual graphitization, a polyimide film with a thickness of 75 μm made by Apical NPI (manufactured by Kaneka Corporation) produced in the same manner as described above was used.

(Reference Example 1)
A polyimide film A having a length of 20 m, a width of 250 mm and a thickness of 75 μm is wound around a cylindrical carbonaceous core having an outer diameter of 150 mm, heated to 1000 ° C. in a nitrogen atmosphere using an electric furnace, and then at 1000 ° C. Carbonization treatment (carbonization treatment) was performed by heat treatment for 1 hour. Subsequently, the temperature was raised to 2800 ° C. in an argon atmosphere using an ultrahigh temperature furnace, and the maximum temperature was maintained for 1 hour. Thereafter, it was cooled to obtain a graphite film.

(Reference Example 2)
Graphite film in the same manner as in Reference Example 1, except that polyimide film A having a length of 30 m, a width of 250 mm, and a thickness of 75 μm was used for the polyimide film, and a cylindrical carbonaceous material having an outer diameter of 250 mm was used for the cylindrical carbonaceous core. Was made.

(Example 3)
A polyimide film A having a length of 20 m, a width of 250 mm and a thickness of 75 μm is attached to the inner surface of a cylindrical container charcoal having an inner diameter of 300 mm, heated to 1000 ° C. in a nitrogen atmosphere using an electric furnace, and then at 1000 ° C. Carbonization treatment (carbonization treatment) was performed by heat treatment for 1 hour. Subsequently, the temperature was raised to 3000 ° C. under an argon atmosphere using an ultra-high temperature furnace, and the maximum temperature was maintained for 1 hour. Thereafter, it was cooled to obtain a graphite film.

(Reference Example 4)
A polyimide film A having a length of 20 m, a width of 250 mm and a thickness of 75 μm is wound around a cylindrical carbonaceous core having an outer diameter of 150 mm, heated to 1000 ° C. in a nitrogen atmosphere using an electric furnace, and then at 1000 ° C. Carbonization treatment (carbonization treatment) was performed by heat treatment for 1 hour. Subsequently, a carbonized core wrapped with a carbonized film is held in a graphite container, covered with carbon powder mainly composed of coke, and then held in a graphite energizable container having an inner diameter of 450 mm. And covered with carbon powder. Thereafter, the atmosphere was not heated, and a DC voltage was applied to the entire container and carbon powder to heat to 3000 ° C., and a graphite film was produced.

(Reference Example 5)
Graphite film in the same manner as in Reference Example 4 except that a polyimide film A having a length of 30 m, a width of 250 mm, and a thickness of 75 μm was used for the polyimide film, and a cylindrical carbonaceous material having an outer diameter of 250 mm was used for the cylindrical carbonaceous core. Was made.

(Reference Example 6)
Graphite film in the same manner as in Reference Example 4 except that polyimide film A having a length of 45 m, a width of 250 mm, and a thickness of 75 μm was used for the polyimide film, and a cylindrical carbonaceous material having an outer diameter of 250 mm was used for the cylindrical carbonaceous core. Was made.

(Reference Example 7)
Graphite film in the same manner as in Reference Example 4 except that a polyimide film A having a length of 30 m, a width of 250 mm, and a thickness of 125 μm was used for the polyimide film, and a cylindrical carbonaceous material having an outer diameter of 250 mm was used for the cylindrical carbonaceous core. Was made.

(Reference Example 8)
A polyimide film A having a length of 20 m, a width of 250 mm, and a thickness of 75 μm is wound around a cylindrical carbonaceous core having an outer diameter of 300 mm, heated to 1000 ° C. in a nitrogen atmosphere using an electric furnace, and then at 1000 ° C. Carbonization treatment (carbonization treatment) was performed by heat treatment for 1 hour. After the obtained carbonized film was wound around a carbonaceous core having an outer diameter of 250 mm, the carbonaceous core and the carbonized film wound around were held in a graphite container and covered with carbon powder mainly composed of coke. Furthermore, it was held in a graphite energizable container having an inner diameter of 450 mm and covered with carbon powder. Thereafter, the atmosphere was not heated, and a DC voltage was applied to the entire container and carbon powder to heat to 3000 ° C., and a graphite film was produced.

(Reference Example 9)
Graphite film in the same manner as in Reference Example 4 except that polyimide film B having a length of 30 m, a width of 250 mm, and a thickness of 75 μm was used for the polyimide film, and a cylindrical carbonaceous material having an outer diameter of 250 mm was used for the cylindrical carbonaceous core. Was made.

(Example 10)
A polyimide film A having a length of 20 m, a width of 250 mm and a thickness of 75 μm is attached to the inner surface of a cylindrical container charcoal having an inner diameter of 300 mm, heated to 1000 ° C. in a nitrogen atmosphere using an electric furnace, and then at 1000 ° C. Carbonization treatment (carbonization treatment) was performed by heat treatment for 1 hour. Subsequently, a graphite film was produced in the same manner as in Reference Example 4.

(Comparative Example 1)
Graphite film in the same manner as in Reference Example 1 except that a polyimide film A having a length of 20 m, a width of 180 mm, and a thickness of 75 μm was used for the polyimide film, and a cylindrical carbonaceous material having an outer diameter of 60 mm was used for the cylindrical carbonaceous core. Was made.

(Comparative Example 2)
Graphite film in the same manner as in Reference Example 1 except that a polyimide film A having a length of 30 m, a width of 180 mm and a thickness of 75 μm was used for the polyimide film, and a cylindrical carbonaceous material having an outer diameter of 100 mm was used for the cylindrical carbonaceous core. Was made.

(Comparative Example 3)
Although an attempt was made to wind a carbonized polyimide film A having a length of 20 m, a width of 180 mm, and a thickness of 75 μm around a cylindrical carbonaceous material having an outer diameter of 100 mm, the film was damaged at the time of winding.

  Table 1 shows the thermal diffusivities of the graphite films obtained in Reference Examples 1, 2, 4 to 9, Examples 3 and 10, and Comparative Examples 1 to 3.

The progress of graphitization is determined by measuring the thermal diffusivity in the film surface direction, and the higher the thermal diffusivity, the more remarkable the graphitization. The thermal diffusivity was measured at 10 Hz in an atmosphere of 20 ° C. using a thermal diffusivity measuring apparatus (“LaserPit” available from ULVAC Riko Co., Ltd.) by an optical alternating current method.
The flatness of the graphite film does not cause wrinkles or breakage or roll when it is graphitized by wrapping around a carbonaceous core or graphitized along the inner surface of a carbonaceous container. “○” indicates that the cylindrical history can be easily stretched, and “×” indicates that the cylindrical history cannot be stretched and needs to be rolled.

The thermal diffusivity of the graphite films obtained in Reference Examples 1, 2, 4 to 9, and Examples 3 and 10 shows high thermal conductivity of 7.5 × 10 ⁻⁴ m ² / S or more at any level. Although the graphitized cylindrical history remained, the cylindrical history could be easily removed without rolling. On the other hand, the thermal diffusivity of the graphite films obtained in Comparative Examples 1 and 2 was 6.9 × 10 ⁻⁴ m ² / S or less at any level, and Reference Examples 1, ^{2, 4 to} 9, and Example 3 , 10 is inferior, and the cylindrical history remains strongly, and it was necessary to roll. In addition, due to the large number of windings, wrinkles were partially contained after heat treatment such as carbonization and graphitization. In particular, the inner side of the winding, the larger the wrinkles, and some fusion was also confirmed,
In addition, comparing Reference Examples 1 and 2 and Example 3 with Comparative Examples 1 and 2, the thermal diffusivity generally increases in the order of Comparative Example 1, Comparative Example 2, Reference Example 1, Reference Example 2, and Example 3. Was. The reason for this is that in Comparative Examples 1 and 2, a carbonaceous core having an outer diameter of 60, 80 mm is used as the carbonaceous core around which the raw material film is wound, whereas in Reference Examples 1, 2, and Example 3, the outer diameter is used. A carbonaceous core having a diameter of 150, 250 mm and a carbonaceous container having an inner diameter of 300 mm are used, and the outer diameter and inner diameter of the carbonaceous core and the carbonaceous container are increased. The reason why the thermal diffusivity increases by increasing the outer diameter and inner diameter is that graphitization proceeds smoothly and the graphene layer develops flat because the raw film is graphitized with a small curvature This is because it is easier to do. In addition, the increase in the diameter makes it possible to reduce the number of windings, and the heat history applied to the film during the heat treatment varies, which is considered to have deteriorated the physical properties.

  Moreover, the graphite films obtained in Reference Examples 4 to 9 and Example 10 were superior in thermal diffusivity to the graphite films obtained in Reference Examples 1 and 2 and Example 3. In these examples and reference examples, the raw material film is held in a container that can be energized, and the material film is graphitized while being energized by applying voltage to the container. The heat generated by the raw material film itself contributes, and the film is heated uniformly inside and on the surface, and is heated evenly from the periphery of the film, so a graphite film with better electrical and thermal conductivity than before can be obtained. I think I was able to get it. Furthermore, even when a raw material film having a thickness of about 125 μm is used, since the film is uniformly heated from the inside, the surface, and the periphery of the film, the surface and the inside are graphitized at the same time to prevent generation of decomposition gas on the surface layer. It is thought that a graphite film excellent in electrical conductivity and thermal conductivity with a large thickness could be obtained without forming a layer, making it easy for the cracked gas inside to escape, and causing no film breakage due to the cracked gas. In addition, when using a large carbonaceous core or carbonaceous container with an outer diameter / inner diameter exceeding 150 mm as in the present example / reference example, when graphitizing by atmospheric heating, the temperature during the heat treatment However, in Reference Examples 4 to 9 and Example 10, since graphitization was performed by energization heating, the carbonaceous core and the carbonaceous container were uniformly heated, and the quality was excellent. I think that graphite was obtained.

  On the other hand, in Comparative Examples 1 and 2, since the heating is performed in an inert gas atmosphere, the heating is performed from the surface of the raw material film by the heat conduction of the portion in contact with the heater and the atmospheric gas, and the radiant heat from the heater. It is thought that graphitization progressed unevenly on the surface, and the thermal conductivity of the entire film was lowered. In particular, when the raw material film is thick, graphitization proceeds from the surface, so that it is difficult for the decomposition gas to be emitted from the inside, and the film is easily broken due to excessive decomposition gas release.

  In the graphite films obtained in Reference Examples 5 and 9, Reference Example 9 was superior. The reason why Reference Example 9 was superior was that Reference Example 8 had a higher surface orientation of the starting material and was manufactured under sequence control, and therefore, it was considered that the rearrangement of molecules during graphitization was facilitated. . Moreover, since the carbon ratio is higher as the degree of surface orientation of the starting material is higher, it is considered that the amount of cracked gas generated is small and graphitization proceeds smoothly.

1 Polyimide film 2 Wedge-shaped sheet 3 Wedge-shaped sheet width 4 Sodium light 5 Interference fringes

Claims (12)

  A method for producing a graphite film, wherein a raw material film comprising a polymer film and / or a carbonized polymer film is graphitized, wherein the raw material film is held on the inner surface of a carbonaceous container and graphitized. A method for producing a graphite film.   The method for producing a graphite film according to claim 1, comprising a step of graphitizing while applying voltage and applying current.   3. The method for producing a graphite film according to claim 1, wherein the energization is performed in a state where carbon powder is present around the container. 4.   The said container is cylindrical shape, The manufacturing method of the graphite film in any one of Claims 1-3 characterized by the above-mentioned.   The method for producing a graphite film according to claim 1, wherein the container is a cylindrical container having an inner diameter of 200 mm or more.   The polymer film is made of polyimide, polyamide, polyoxadiazole, polybenzothiazole, polybenzobisthiazole, polybenzoxazole, polybenzobisoxazole, polyparaphenylene vinylene, polybenzimidazole, polybenzobisimidazole, polythiazole. It consists of at least 1 or more types of polymer chosen from the inside, The manufacturing method of the graphite film in any one of Claims 1-5 characterized by the above-mentioned.   The method for producing a graphite film according to claim 6, wherein the polymer film is a polyimide film having a birefringence of 0.08 or more.   The method for producing a graphite film according to claim 6, wherein the polymer film is a polyimide film having a birefringence of 0.12 or more.   The polymer film is a polyimide film produced by imidizing pyromellitic dianhydride and polyamic acid containing p-phenylenediamine using a dehydrating agent and an imidization accelerator, The manufacturing method of the graphite film in any one of Claims 6-8.   The polymer film uses a diamine and an acid dianhydride to synthesize a prepolymer having the acid dianhydride at both ends, and reacts the prepolymer with a diamine different from the above to synthesize a polyamic acid. It is a polyimide film produced by imidating an acid, The manufacturing method of the graphite film in any one of Claims 6-8 characterized by the above-mentioned.   The method for producing a graphite film according to any one of claims 6 to 10, wherein the polymer film is a polymer film having a length of 15 m or more.   The method for producing a graphite film according to any one of claims 6 to 10, wherein the polymer film is a polymer film having a length of 15 m or more and a width of 250 mm or more.

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