EP0579879A1 - Production method of expanded graphite sheet and expanded graphite sheet obtained thereby - Google Patents
Production method of expanded graphite sheet and expanded graphite sheet obtained thereby Download PDFInfo
- Publication number
- EP0579879A1 EP0579879A1 EP92306679A EP92306679A EP0579879A1 EP 0579879 A1 EP0579879 A1 EP 0579879A1 EP 92306679 A EP92306679 A EP 92306679A EP 92306679 A EP92306679 A EP 92306679A EP 0579879 A1 EP0579879 A1 EP 0579879A1
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- European Patent Office
- Prior art keywords
- expanded graphite
- expanded
- sheet
- graphite sheet
- graphite
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- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 title claims abstract description 69
- 239000010439 graphite Substances 0.000 title claims abstract description 69
- 229910002804 graphite Inorganic materials 0.000 title claims abstract description 69
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000002245 particle Substances 0.000 claims abstract description 22
- 239000004760 aramid Substances 0.000 claims abstract description 17
- 229920003235 aromatic polyamide Polymers 0.000 claims abstract description 16
- 238000000034 method Methods 0.000 claims abstract description 16
- 239000002002 slurry Substances 0.000 claims abstract description 13
- 239000000835 fiber Substances 0.000 claims abstract description 9
- 230000008569 process Effects 0.000 claims abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 239000011230 binding agent Substances 0.000 claims description 16
- 239000012783 reinforcing fiber Substances 0.000 claims description 7
- 238000000227 grinding Methods 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 4
- 238000005452 bending Methods 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 2
- 230000003014 reinforcing effect Effects 0.000 claims 1
- 239000000463 material Substances 0.000 description 13
- 239000000203 mixture Substances 0.000 description 12
- 229920006231 aramid fiber Polymers 0.000 description 8
- 238000007789 sealing Methods 0.000 description 8
- 239000004816 latex Substances 0.000 description 7
- 229920000126 latex Polymers 0.000 description 7
- 238000001035 drying Methods 0.000 description 5
- 239000010425 asbestos Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 229910052895 riebeckite Inorganic materials 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000654 additive Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 238000010009 beating Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000012784 inorganic fiber Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000012744 reinforcing agent Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000004438 BET method Methods 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 229920000914 Metallic fiber Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 229920001973 fluoroelastomer Polymers 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000003232 water-soluble binding agent Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H13/00—Pulp or paper, comprising synthetic cellulose or non-cellulose fibres or web-forming material
- D21H13/36—Inorganic fibres or flakes
- D21H13/46—Non-siliceous fibres, e.g. from metal oxides
- D21H13/50—Carbon fibres
-
- D—TEXTILES; PAPER
- D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
- D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
- D21H13/00—Pulp or paper, comprising synthetic cellulose or non-cellulose fibres or web-forming material
- D21H13/10—Organic non-cellulose fibres
- D21H13/20—Organic non-cellulose fibres from macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D21H13/26—Polyamides; Polyimides
Definitions
- the present invention relates to an expanded graphite and production method thereof and, more particularly, to a heat resistant and asbestos-free graphite sheet which is utilized in gasket or the like for sealing various joints of internal combustion engine and in other industrial purposes, and a production method thereof.
- joint sheets and beater sheets mainly composed of asbestos have been used as conventional gasket or the like.
- Use of asbestos has been increasingly regulated due to its harmfulness for the health.
- the present invention was made to solve the above discussed problem pertinent to the graphite sheet, particulary, to expanded graphite sheet, and has an object of developing a novel asbestos-free expanded graphite sheet of superior mechanical strength.
- a method for producing the asbestos-free expanded graphite sheet according to the invention comprises the steps of: compressing a graphite preliminaly expanded to not less than 50 times as large as normal state in average so as to be 0.02 to 0.3 g/cm 3 in bulk density; grinding the compressed graphite: suspending the above ground graphite into water in the presence of a binder together with a reinforcing fiber formed by fibrilating an aramid pulp fiber so as to be not less than 3.0 m 2 /g in specific surface, thus obtaining a paper making slurry; and wet-processing the slurry to be formed into a sheet.
- the expanded graphite is first compressed to a predetermined bulk density.
- a graphite expanded to not less than 50 times as large as normal state in average is not uniformly suspended into water to be a slurry no matter how it is ground, and not made into a paper due to floating of graphite particles on the surface of the water.
- a method of utilizing a small amount of hydrophilic solvent such as acetone is known, but graphite particles tend to still float on the water even if employing such solvent, and this method is not a definite means of solution to the problem.
- the expanded graphite particles are first subject to compression to be 0.02 to 0.3 g/cm 3, preferably 0.05 to 0.15 g/cm 3, in bulk density.
- the bulk density is smaller than 0.02 g/cm 3
- expanded gas existing in the hollow pores of the expanded graphite particles is not discharged, but the graphite particles (i.e., material) remain floating no matter how they are ground and stirred in the water.
- the bulk density is larger than 0.3 g/cm 3
- the ground expanded graphite does not lose the required characteristics, and is successfully suspended into water and fixed to the aramid pulp fiber resulting in an ideal paper material.
- any means may be employed in principle as far as a required bulk density is obtained thereby, and in particular it is preferable to employ compressive means capable of continuously compressing the material in combination of a horizontal conveyor and an inclined conveyor.
- the compression for obtaining a bulk density of 0.05 to 0.1 g/cm 3 according to the invention may be achieved by the known method as disclosed in the Japanese Patent Publication No. 71694/1978 in which casing of wire gauze is used. In this known method, however, mass production is difficult.
- an expanded graphite which has been expanded to not less than 50 times in average as large as normal state is employed. Accordingly, not only the graphite particles alone expanded to not less than 50 times but also a mixture of a graphite expanded to be less than 50 times with another graphite expanded to not less than 50 times so as to be not less than 50 times in its entirety may be employed in the invention.
- expansion of less than 50 times in average brings about decline in flexibility and sealing performance of the sheet.
- the compressed graphite is then ground in the invention.
- either wet process or dry process can be employed.
- the compressed graphite is ground in a state preliminarily mixed with water, and the ground objects thus obtained are used as they are to be prepared into slurry.
- a customary mixer type grinder as grinder means.
- a beater used in the field of paper making. Size of the ground objects is usually not larger than 50 meshes, preferably about 60 to 100 meshes.
- the compressed graphite is ground to the same size as the foregoing wet process in the absence of water. It is preferable to employ a grinder utilizing shearing force such as high speed mixer, for example.
- the objects ground by dry process may be mixed with water beforehand, then prepared into slurry. It is also preferable to make the ground objects directly into slurry.
- the reinforcing fiber employed in the invention causes the expanded graphite particles to fix thereto in the water and be dispersed evenly without separation when diluted to a required concentration. This function of even or uniform dispersion is a key factor for obtaining an expanded graphite sheet of high strength. To satisfy such conditions without fail, the reinforcing fiber should be of following characteristics:
- a reinforcing fiber composed of pulped para-aramid or meta-aramid fiber of superior heat resistance can satisfy the mentioned conditions most effectively.
- Aramid fiber itself is well known, and various kinds of conventionally known aramid fibers can be used in the invention. Any of those aramid fibers is employed through fibrilation so as to be of a required specific surface. Means of fibrilation are not particularly defined and any known means can be employed. Specific surface is required to be not less than 3.0 m 2 /g , preferably 5.0 to 8.0 m 2 /g . If less than 3.0 m 2 /g , there arises a disadvantage of poor fixation of graphite particles.
- aramid fiber As for amount of use of such aramid fiber in the slurry, 3 to 25 parts by weight of aramid fiber, preferably 5 to 15 parts by weight, are used.
- a binder is also used in the invention.
- Water-soluble binder, emulsion type binder and powder binder are all employable, and among them emulsion type is particularly preferable because this type of binder is composed of fine particles easy to be dispersed in water and fixed gradually.
- Latex of NR, NBR, CR and acrylic rubber is preferably added according to specific use considering such characteristics as strength, heat resistance, oil resistance, etc. When a further high heat resistance is required, it is preferable to employ phenol resin and NBR latex together or emulsion of silicon rubber and fluoro-rubber and the like.
- wet process For preparing a paper-making slurry into a paper, wet process is usually employed. Conventionally known conditions for such wet process itself and paper making apparatus can be appropriately utilized as they are.
- the sheet thus obtained from an expanded graphite according to the invention is very high in mechanical strength, superior in heat resistance and sealing performance, sufficient in flexibility, and therefore quite preferably formed into gaskets for sealing various joint surfaces of internal combustion engine or for other industrial uses.
- the specific surfaces are measured by BET method using a mixed gas of N2 (30%) and He (70%).
- the sheet of above composition and function according to the present invention mechanical strength and flexibility are significantly improved as compared with the flexible expanded graphite sheet according to the prior art, and easy to handle in practical use. Furthermore, other characteristics such as water resistance, oil resistance are also improved thereby substantially satisfying JIS standard on asbestos joint sheet.
- the sheet of the mentioned features according to the invention can be widely used not only as gasket for industries in general but also as gasket for sealing various joints in internal combustion engine.
- Figures 1 and 2 are graphs respectively showing a relation between mix proportion of graphite sheet material and tensile strength, and a relation between mix proportion of graphite sheet material and stress relaxation.
- the obtained product was then put in a tank equipped with a pickup net and dispersed uniformly, and drained, thus a sheet being obtained.
- the obtained sheet was then subject to suction of water by a suction pump, and dewatering by wrapping it in a felt to be compressed by a press.
- the sheet was then placed in an oven for drying at 120°C, and density of the sheet was adjusted to 1.3 g/cm 3 by passing through calender rollers. Finally crosslinking was carried out at 150°C for 20 minutes.
- a sheet was formed in the same manner as the foregoing Example 1 except that 15 parts of aramid pulp, 75 parts of expanded graphite and 10 parts (calculated in solid) of NBR latex were used.
- 15 parts of aramid pulp, 75 parts of expanded graphite and 10 parts (calculated in solid) of NBR latex were used.
- a cationic flocculant such as aqueous solution of 0.1 part of Sanflock CH799P (produced by Sanyo Chemical Industries) was added.
- a sheet was formed in the same manner as the foregoing Examples 1 and 2 except that mix proportion of expanded graphite, aramid pulp and NBR latex was varied as shown in Table 1.
- Characteristics of the flexible expanded graphite sheet obtained in Examples 1 and 2 were measured according to JIS R 3453. Result of the measurement was compared with the standard values of Class 1, 2 and 3 prescribed in JIS R 3453, as shown in Table 2.
- any required sheet can be formed by optionally selecting the addition amount of reinforcing agent and binder.
- Table 1 NBR latex Expanded graphite Aramid pulp Example Group I 5 90 5 3 85 10 1 80 15 4 75 20 5 85 5 6 Group II 10 80 10 7 75 15 2 70 20 8
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- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paper (AREA)
- Sealing Material Composition (AREA)
Abstract
Description
- The present invention relates to an expanded graphite and production method thereof and, more particularly, to a heat resistant and asbestos-free graphite sheet which is utilized in gasket or the like for sealing various joints of internal combustion engine and in other industrial purposes, and a production method thereof.
- Hithereto, joint sheets and beater sheets mainly composed of asbestos have been used as conventional gasket or the like. Use of asbestos, however, has been increasingly regulated due to its harmfulness for the health.
- Flexible expanded graphite sheet has been also known. This sheet is superior in sealing performance and heat resistance, but inferior in mechanical strength. Moreover, the sheet is difficult to handle in practical use and deficient in water resistance and oil resistance.
- In substitution for the mentioned sheets, a sheet has been developed, and in which filler is applied to aramid pulp or inorganic fiber and rubber-like elastic material is utilized as binder. This sheet is produced by either dry process or wet process. However, this sheet is also inferior to asbestos sheet in mechanical strength, heat resistance and sealing performance.
- Under such circumstances, improvement of the flexible expanded graphite has been attempted. For example, in the Japanese Laid-Open Patent Publication (unexamined) No. 124767/1990, it is disclosed that a rubber-like elastic binder is applied to expanded graphite particles to improve the bending breakdown resistance and oil resistance of the sheet, but has not advanced yet to the level of put a single compact thus formed into practical use. In the Japanese Laid-Open Patent Publication (unexamined) No. 288180/1987, another improvement is proposed in which an expanded graphite is impregnated with a thermosetting resin, and the resin is heated and dried to improve mechanical strength and liquid permeability. In this prior art, however, there arises a problem of losing flexibility which is the most important property, and moreover a problem of how to handle the product has not been solved yet. Furthermore, the Japanese Laid-Open Patent Publications (unexamined) Nos. 71578/1985 and 72780/1988 disclose a method for mixing expanded graphite particles with reinforcing fiber or binder. Advantage of these prior arts is not sufficient to overcome the problem of brittleness and poor mechanical strength.
- The present invention was made to solve the above discussed problem pertinent to the graphite sheet, particulary, to expanded graphite sheet, and has an object of developing a novel asbestos-free expanded graphite sheet of superior mechanical strength.
- In order to accomplish the foregoing object a method for producing the asbestos-free expanded graphite sheet according to the invention comprises the steps of: compressing a graphite preliminaly expanded to not less than 50 times as large as normal state in average so as to be 0.02 to 0.3g/cm³ in bulk density; grinding the compressed graphite: suspending the above ground graphite into water in the presence of a binder together with a reinforcing fiber formed by fibrilating an aramid pulp fiber so as to be not less than 3.0m²/g in specific surface, thus obtaining a paper making slurry; and wet-processing the slurry to be formed into a sheet.
- In the invention, the expanded graphite is first compressed to a predetermined bulk density. A graphite expanded to not less than 50 times as large as normal state in average is not uniformly suspended into water to be a slurry no matter how it is ground, and not made into a paper due to floating of graphite particles on the surface of the water. In this respect, a method of utilizing a small amount of hydrophilic solvent such as acetone is known, but graphite particles tend to still float on the water even if employing such solvent, and this method is not a definite means of solution to the problem.
- Thus, no uniform sheet is obtained with the conventional ground graphite as it is even if trying to make them into a paper. If something like a sheet is obtained, mechanical strength thereof is very poor and not suited for practical use. For that reason, in the invention, the expanded graphite particles are first subject to compression to be 0.02 to 0.3g/cm³, preferably 0.05 to 0.15g/cm³, in bulk density.
- If the bulk density is smaller than 0.02g/cm³, expanded gas existing in the hollow pores of the expanded graphite particles is not discharged, but the graphite particles (i.e., material) remain floating no matter how they are ground and stirred in the water. On the contrary, if the bulk density is larger than 0.3g/cm³, not only the grinding in the water is difficult but also the ground material being transformed into grains comes to lose the characteristics of expanded graphite. When grinding a material in the range of the mentioned bulk density, the ground expanded graphite does not lose the required characteristics, and is successfully suspended into water and fixed to the aramid pulp fiber resulting in an ideal paper material.
- As for the means for compressing the graphite expanded 50 times as large as normal state, any means may be employed in principle as far as a required bulk density is obtained thereby, and in particular it is preferable to employ compressive means capable of continuously compressing the material in combination of a horizontal conveyor and an inclined conveyor.
- In this respect, the compression for obtaining a bulk density of 0.05 to 0.1g/cm³ according to the invention may be achieved by the known method as disclosed in the Japanese Patent Publication No. 71694/1978 in which casing of wire gauze is used. In this known method, however, mass production is difficult.
- In the invention, an expanded graphite which has been expanded to not less than 50 times in average as large as normal state is employed. Accordingly, not only the graphite particles alone expanded to not less than 50 times but also a mixture of a graphite expanded to be less than 50 times with another graphite expanded to not less than 50 times so as to be not less than 50 times in its entirety may be employed in the invention. Anyway, it is clearly acknowledged that expansion of less than 50 times in average brings about decline in flexibility and sealing performance of the sheet.
- The compressed graphite is then ground in the invention. In the grinding step, either wet process or dry process can be employed. In the wet process, the compressed graphite is ground in a state preliminarily mixed with water, and the ground objects thus obtained are used as they are to be prepared into slurry. It is preferable to employ a customary mixer type grinder as grinder means. It is also preferable to employ a beater used in the field of paper making. Size of the ground objects is usually not larger than 50 meshes, preferably about 60 to 100 meshes.
- In the dry process, the compressed graphite is ground to the same size as the foregoing wet process in the absence of water. It is preferable to employ a grinder utilizing shearing force such as high speed mixer, for example. The objects ground by dry process may be mixed with water beforehand, then prepared into slurry. It is also preferable to make the ground objects directly into slurry.
- The reinforcing fiber employed in the invention causes the expanded graphite particles to fix thereto in the water and be dispersed evenly without separation when diluted to a required concentration. This function of even or uniform dispersion is a key factor for obtaining an expanded graphite sheet of high strength. To satisfy such conditions without fail, the reinforcing fiber should be of following characteristics:
- (1) That the reinforcing fiber is neutral or positive in the aspect of ion.
As the expanded graphite particles is anionic in the water, perfect fixation thereof is not achieved no matter how fibrilation is carried out by beating a fiber of the same ion as is done in cellulose fiber. - (2) That after the steps of beating the fiber and fibrilating it, specific surface of the fiber is not less than 3.0m²/g.
As specific surface of the expanded graphite particles is large, it becomes necessary that the fiber for causing the graphite particles to fix thereto is also fibrilated to be not less than 3.0m²/g in specific surface, so that absorption may be physically easy. In this sense, the technical advantage of reinforcement is not achieved by employing any inorganic fiber or metallic fiber. - In consequence, a reinforcing fiber composed of pulped para-aramid or meta-aramid fiber of superior heat resistance can satisfy the mentioned conditions most effectively.
- Aramid fiber itself is well known, and various kinds of conventionally known aramid fibers can be used in the invention. Any of those aramid fibers is employed through fibrilation so as to be of a required specific surface. Means of fibrilation are not particularly defined and any known means can be employed. Specific surface is required to be not less than 3.0m²/g, preferably 5.0 to 8.0m²/g. If less than 3.0m²/g, there arises a disadvantage of poor fixation of graphite particles.
- As for amount of use of such aramid fiber in the slurry, 3 to 25 parts by weight of aramid fiber, preferably 5 to 15 parts by weight, are used.
- To improve the mechanical strength of the obtained sheet, a binder is also used in the invention. Water-soluble binder, emulsion type binder and powder binder are all employable, and among them emulsion type is particularly preferable because this type of binder is composed of fine particles easy to be dispersed in water and fixed gradually. Latex of NR, NBR, CR and acrylic rubber is preferably added according to specific use considering such characteristics as strength, heat resistance, oil resistance, etc. When a further high heat resistance is required, it is preferable to employ phenol resin and NBR latex together or emulsion of silicon rubber and fluoro-rubber and the like.
- Each of the mentioned materials is then suspended into water to be made into a paper-making slurry in the following mix proportion:
- Expanded graphite particles:
- 60 to 90 parts by weight
- Aramid pulp :
- 3 to 25 parts by weight
- Binder :
- 1 to 20 parts by weight
- Expanded graphite particles:
- 70 to 85 parts by weight
- Aramid pulp :
- 5 to 10 parts by weight
- Binder :
- 3 to 10 parts by weight
- For preparing a paper-making slurry into a paper, wet process is usually employed. Conventionally known conditions for such wet process itself and paper making apparatus can be appropriately utilized as they are.
- The sheet thus obtained from an expanded graphite according to the invention is very high in mechanical strength, superior in heat resistance and sealing performance, sufficient in flexibility, and therefore quite preferably formed into gaskets for sealing various joint surfaces of internal combustion engine or for other industrial uses.
- In addition, the specific surfaces are measured by BET method using a mixed gas of N₂ (30%) and He (70%).
- In the sheet of above composition and function according to the present invention, mechanical strength and flexibility are significantly improved as compared with the flexible expanded graphite sheet according to the prior art, and easy to handle in practical use. Furthermore, other characteristics such as water resistance, oil resistance are also improved thereby substantially satisfying JIS standard on asbestos joint sheet. The sheet of the mentioned features according to the invention can be widely used not only as gasket for industries in general but also as gasket for sealing various joints in internal combustion engine.
- Other objects, features and advantages of the invention will become apparent in the course of the following description of the preferred embodiment with reference to the accompanying drawings.
- Figures 1 and 2 are graphs respectively showing a relation between mix proportion of graphite sheet material and tensile strength, and a relation between mix proportion of graphite sheet material and stress relaxation.
- Several examples of the present invention are hereinafter described in detail, although the invention is not restricted thereto. In addition, unless otherwise specified herein, unit is shown in part by weight throughout the examples.
- 200 parts of water and 10 parts of aramid fiber pulp (trade name: Twalon pulp 1096 produced by Aczo) were placed in a mixer, then the pulp was stirred for about five minutes, beaten, and dropped into a mixing chest together with additional 3000 parts of water (Specific surface of the pulp at this time was 7.5m²/g).
- In the meantime, 85 parts of graphite particles expanded to 150 times as large as normal state were compressed to form a sponge so that bulk density thereof was 0.08g/cm³. This material was placed into the mixer together with 2000 parts of water, then stirred, ground and dropped into the mixing chest, whereby the material was mixed with the foregoing aramid pulp. After stirring for 1 to 2 minutes, the particles of expanded graphite were coagulated utilizing the aramid pulp as nucleus, thus a solution of even dispersion being obtained. Then, 5 parts (calculated in solid) of NB latex (trade name: Nippol 1571 produced by Nippon Zeon) were added, and fixed after stirring for 3 to 4 minutes. In this step, because the mixed amount of aramid pulp was rather small, the NBR latex was fixed only by the stirring step alone. A small amount of white zinc was also added as assistant crosslinking agent for NBR.
- The obtained product was then put in a tank equipped with a pickup net and dispersed uniformly, and drained, thus a sheet being obtained. The obtained sheet was then subject to suction of water by a suction pump, and dewatering by wrapping it in a felt to be compressed by a press. The sheet was then placed in an oven for drying at 120°C, and density of the sheet was adjusted to 1.3g/cm³ by passing through calender rollers.
Finally crosslinking was carried out at 150°C for 20 minutes. - A sheet was formed in the same manner as the foregoing Example 1 except that 15 parts of aramid pulp, 75 parts of expanded graphite and 10 parts (calculated in solid) of NBR latex were used. In this example, since increased amount of pulp and binder was used, poor fixation of the late was forcast. To meet this, in the fixation, a cationic flocculant such as aqueous solution of 0.1 part of Sanflock CH799P (produced by Sanyo Chemical Industries) was added.
- A sheet was formed in the same manner as the foregoing Examples 1 and 2 except that mix proportion of expanded graphite, aramid pulp and NBR latex was varied as shown in Table 1.
- Characteristics of the flexible expanded graphite sheet obtained in Examples 1 and 2 were measured according to JIS R 3453. Result of the measurement was compared with the standard values of
Class 1, 2 and 3 prescribed in JIS R 3453, as shown in Table 2. - It is clearly understood from Table 2 that the characteristics of respective sheets in Examples 1 and 2 satisfy the standard values of JIS R 3453.
- Particularly in the flexibility test "performed by bending a test piece by 180° along an iron rod of which diameter is twelve times as thick as the test piece" prescribed in this standard, no crack was recognized at all in the sheets (Examples 1 and 2) as shown in Table 2.
- As comparative examples, several graphite sheets prepared just by compressing an expanded graphite alone without aramid fiber and binder (for example, trade name: Permafoil or PF sheet produced by Toyo Tanso) were subject to the same tests. In the flexibility test, all of these comparative examples were found cracked.
- The foregoing characteristics of the sheet according to the invention brings about a very desirable fluid sealing performance when utilizing the sheet as gasket material.
- On every sheet obtained in the foregoing Examples 1 to 8 (i.e., for each of the sheets with varied addition amount of reinforcing agent and binder), a relation between variation (mix proportion) of the additives and tensile strength and a relation between variation (mix proportion) of the additives and stress relaxation were measured. Results of the measurement are shown in Figure 1 (tensile strength) and Figure 2 (stress relaxation) respectively. In these graphs, dot line shows a case when mix proportion of NBR is 10%, and solid line shows another case when the mix proportion thereof is 5%.
- It is clearly understood from Figures 1 and 2 that when varying addition amount, tensile strength and stress relaxation of the sheet are also varied as accordingly. More specifically, when increasing mix proportion of these additives, tensile strength of the sheet becomes large, while stress relaxation being one of heat resistance indexes is decreased. As a result, any required sheet can be formed by optionally selecting the addition amount of reinforcing agent and binder.
Table 1 NBR latex Expanded graphite Aramid pulp Example Group I 5 90 5 3 85 10 1 80 15 4 75 20 5 85 5 6 Group II 10 80 10 7 75 15 2 70 20 8
Claims (6)
- A method for producing an expanded graphite sheet, characterized in that(A) compressed and ground graphite particles obtained by compressing an expanded graphite preliminarily expanded to not less than 50 times as large as normal state in average to be 0.02 to 0.3g/cm³ in bulk density and grinding the compressed graphite particles;(B) a reinforcing fiber formed by fibrilating an aramid pulp fiber so as to be not less than 3.0m²/g in specific surface;(C) a binder; and(D) waterare suspended together to be transformed into a paper making slurry; and said slurry being subject to wet process to be prepared into a sheet.
- A method for producing an expanded graphite sheet according to claim 1, wherein 60 to 95 parts by weight of said (A), 3 to 25 parts by weight of said (B) and 1 to 20 parts by weight of said (C) are mixed together.
- A method for producing an expanded graphite sheet according to claim 1, wherein the compressed expanded graphite is ground by wet process.
- An expanded graphite sheet produced by the method according to claim 1.
- An expanded graphite sheet produced by the method according to claim 2.
- An expanded and compressed graphite sheet in which no crack (visibly recognized from outside to inside) occurs as a result of a test performed by picking up three test pieces each comprising a reinforcing aramid pulp fiber, a binder and graphite particles, and 25×150m/m in dimensions, and bending each of the test pieces by 180° along an iron rod of which diameter is twelve times as thick as the test piece.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3085713A JP2931882B2 (en) | 1991-01-23 | 1991-01-23 | Manufacturing method of expanded graphite sheet |
| EP92306679A EP0579879B1 (en) | 1991-01-23 | 1992-07-21 | Production method of expanded graphite sheet and expanded graphite sheet obtained thereby |
| DE69205421T DE69205421T2 (en) | 1991-01-23 | 1992-07-21 | A process for producing an expanded graphite sheet and an expanded graphite sheet obtained by this process. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3085713A JP2931882B2 (en) | 1991-01-23 | 1991-01-23 | Manufacturing method of expanded graphite sheet |
| EP92306679A EP0579879B1 (en) | 1991-01-23 | 1992-07-21 | Production method of expanded graphite sheet and expanded graphite sheet obtained thereby |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0579879A1 true EP0579879A1 (en) | 1994-01-26 |
| EP0579879B1 EP0579879B1 (en) | 1995-10-11 |
Family
ID=26132113
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP92306679A Expired - Lifetime EP0579879B1 (en) | 1991-01-23 | 1992-07-21 | Production method of expanded graphite sheet and expanded graphite sheet obtained thereby |
Country Status (3)
| Country | Link |
|---|---|
| EP (1) | EP0579879B1 (en) |
| JP (1) | JP2931882B2 (en) |
| DE (1) | DE69205421T2 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6451486B1 (en) | 2000-05-01 | 2002-09-17 | The Gillette Company | Battery cathode including a mixture of manganese dioxide with carbon particles of expanded and non-expanded graphite |
| EP1518842A1 (en) * | 2003-09-23 | 2005-03-30 | Advanced Energy Technology Inc. | Reactive additive that promotes material flow for moulding compounds |
| US6921610B2 (en) | 2001-07-11 | 2005-07-26 | The Gillette Company | Battery |
| GB2414232B (en) * | 2003-03-31 | 2007-08-01 | Young Woo Shin | Manufacturing method of expanded graphite products |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1999010598A1 (en) * | 1997-08-26 | 1999-03-04 | Toyo Tanso Kabushiki Kaisya | Expanded graphite sheet for electromagnetic wave shielding and process for producing the same |
| EP1209950A4 (en) * | 1999-07-22 | 2005-04-20 | Toyo Tanso Co | Heating element |
| JP4747131B2 (en) * | 2007-04-26 | 2011-08-17 | 日本ピラー工業株式会社 | Sheet gasket |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1992002354A1 (en) * | 1990-08-01 | 1992-02-20 | Mcallister Richard G | High modulus media of reinforcing materials and thermoplastic fibrets |
-
1991
- 1991-01-23 JP JP3085713A patent/JP2931882B2/en not_active Expired - Lifetime
-
1992
- 1992-07-21 EP EP92306679A patent/EP0579879B1/en not_active Expired - Lifetime
- 1992-07-21 DE DE69205421T patent/DE69205421T2/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1992002354A1 (en) * | 1990-08-01 | 1992-02-20 | Mcallister Richard G | High modulus media of reinforcing materials and thermoplastic fibrets |
Non-Patent Citations (2)
| Title |
|---|
| DATABASE WPIL Section Ch, Week 8819, Derwent Publications Ltd., London, GB; Class A88, AN 88-129625 & JP-A-63 072 780 (NIPPON REINZ KK) 2 April 1988 * |
| PATENT ABSTRACTS OF JAPAN vol. 012, no. 301 (C-521)16 August 1988 & JP-A-63 072 780 ( NIPPON REINZ CO LTD ) 2 April 1988 * |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6451486B1 (en) | 2000-05-01 | 2002-09-17 | The Gillette Company | Battery cathode including a mixture of manganese dioxide with carbon particles of expanded and non-expanded graphite |
| US6921610B2 (en) | 2001-07-11 | 2005-07-26 | The Gillette Company | Battery |
| US7132198B2 (en) | 2001-07-11 | 2006-11-07 | The Gillette Company | Battery |
| GB2414232B (en) * | 2003-03-31 | 2007-08-01 | Young Woo Shin | Manufacturing method of expanded graphite products |
| EP1518842A1 (en) * | 2003-09-23 | 2005-03-30 | Advanced Energy Technology Inc. | Reactive additive that promotes material flow for moulding compounds |
Also Published As
| Publication number | Publication date |
|---|---|
| DE69205421D1 (en) | 1995-11-16 |
| JPH04240295A (en) | 1992-08-27 |
| JP2931882B2 (en) | 1999-08-09 |
| DE69205421T2 (en) | 1996-06-05 |
| EP0579879B1 (en) | 1995-10-11 |
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