WO2010029851A1 - フッ素ゴム金属積層板 - Google Patents
フッ素ゴム金属積層板 Download PDFInfo
- Publication number
- WO2010029851A1 WO2010029851A1 PCT/JP2009/064905 JP2009064905W WO2010029851A1 WO 2010029851 A1 WO2010029851 A1 WO 2010029851A1 JP 2009064905 W JP2009064905 W JP 2009064905W WO 2010029851 A1 WO2010029851 A1 WO 2010029851A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fluororubber
- weight
- parts
- metal laminate
- laminate according
- Prior art date
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B15/06—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material of natural rubber or synthetic rubber
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16J—PISTONS; CYLINDERS; SEALINGS
- F16J15/00—Sealings
- F16J15/02—Sealings between relatively-stationary surfaces
- F16J15/06—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces
- F16J15/10—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces with non-metallic packing
- F16J15/12—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces with non-metallic packing with metal reinforcement or covering
- F16J15/121—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces with non-metallic packing with metal reinforcement or covering with metal reinforcement
- F16J15/122—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces with non-metallic packing with metal reinforcement or covering with metal reinforcement generally parallel to the surfaces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/04—Layered products comprising a layer of metal comprising metal as the main or only constituent of a layer, which is next to another layer of the same or of a different material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/18—Homopolymers or copolymers or tetrafluoroethene
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16J—PISTONS; CYLINDERS; SEALINGS
- F16J15/00—Sealings
- F16J15/02—Sealings between relatively-stationary surfaces
- F16J15/06—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16J—PISTONS; CYLINDERS; SEALINGS
- F16J15/00—Sealings
- F16J15/02—Sealings between relatively-stationary surfaces
- F16J15/06—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces
- F16J15/10—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces with non-metallic packing
- F16J15/12—Sealings between relatively-stationary surfaces with solid packing compressed between sealing surfaces with non-metallic packing with metal reinforcement or covering
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D2202/00—Metallic substrate
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D2530/00—Rubber or the like
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/04—Condensation polymers of aldehydes or ketones with phenols only
- C08L61/06—Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
- C08L61/14—Modified phenol-aldehyde condensates
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/25—Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31511—Of epoxy ether
- Y10T428/31529—Next to metal
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
Definitions
- the present invention relates to a fluorine rubber metal laminate. More particularly, the present invention relates to a fluororubber-metal laminate that is effectively used as a gasket for automobiles and the like.
- the purpose of addition of the silane coupling agent is to suppress the rubber flow, that is, to improve the rigidity of the rubber, and the long-term durability such as antifreeze liquid resistance, oil resistance and heat resistance becomes inferior.
- the inorganic filler exhibiting low friction is difficult to disperse and the particle size of the filler becomes large, the seal surface is roughened particularly in a cylinder head gasket or the like which is very thin, around 25 ⁇ m of the product rubber layer thickness. It is easy and has an adverse effect on sealability.
- the metal plate is subjected to chromate treatment or chromate substitution treatment (treatment without hexavalent Cr, treatment with iron phosphate, treatment with zinc phosphate, etc. It is used after performing nonchromate processing).
- chromate treatment has a problem of environmental load
- the rubber metal laminate produced by applying the multi-layer coating method after applying chromate substitution treatment to the metal plate used instead is In view of the complexity of the treatment process, the environmental impact of the product as a whole is large, and the cost is also disadvantageous.
- JP 2004-68886 A JP-A-61-12741
- An object of the present invention is a fluororubber metal laminate in which a vulcanized fluororubber layer is laminated on a metal plate which is not subjected to chromate treatment or chromate replacement treatment, and the sealability, compression resistance, air heat aging resistance, resistance to air
- An object of the present invention is to provide excellent antifreeze liquid resistance, oil resistance, sticking resistance, abrasion resistance and other properties.
- the object of the present invention is as follows: (A) 10 to 50 parts by weight of (B) earthy graphite, (C) 1 to 15 parts by weight of phenol resin, (D) silane coupling, per 100 parts by weight of the polyol vulcanizable fluororubber
- a fluororubber composition containing 1 to 4 parts by weight of an additive, 0.5 to 8 parts by weight of (E) a polyol-based vulcanizing agent and 0.5 to 6 parts by weight of a vulcanization accelerator (F) is applied on a metal plate
- the rubber composition is achieved by vulcanizing and laminating a fluororubber metal laminate.
- the fluororubber composition used to form the fluororubber metal laminate according to the present invention has the following features. (1) By using as a one-component coating agent, ⁇ Because it is Cr free because it is applied to metal plate which is not treated with chromate ⁇ It is not a multilayer coating type, so the VOC emission is small and the environmental impact is small ⁇ The processing cost is reduced because the process is not complicated. be able to (2) By selecting and using specific graphite called earthy graphite, ⁇ Since it is easy to set the particle size of the rubber solution to 20 ⁇ m or less, it is smooth and has excellent initial sealability. • It has less delamination compared to scaly graphite and has non-stickiness, so it has excellent reworkability. (3) By using a phenol resin and a silane coupling agent in combination, ⁇ We can obtain long-term durability such as antifreeze resistance, oil resistance, heat resistance
- metal plate stainless steel plate whose surface is not roughened, SPCC steel plate, aluminum plate, etc., stainless steel plate whose surface is roughened by shot blast, scotch blast, hairline, dull finish, etc., SPCC steel plate, aluminum plate
- solvent degreased, alkaline degreased and the like are used as they are.
- a metal plate having a thickness of about 0.1 to 1 mm is used.
- Polyol-vulcanizable fluororubbers of component (A) which form a fluororubber composition include vinylidene fluoride, hexafluoropropene, pentafluoropropene, trifluoroethylene, trifluorochloroethylene, tetrafluoroethylene, vinyl fluoride Homopolymers, alternating copolymers, or copolymers of these with propylene, such as perfluoroacrylic acid ester, perfluoroalkyl acrylate, perfluoro (methyl vinyl ether), perfluoro (ethyl vinyl ether), perfluoro (propyl vinyl ether), etc.
- Polymers may be mentioned, preferably vinylidene fluoride-hexafluoropropene copolymer, vinylidene fluoride-hexafluoropropene-tetrafluoroethylene terpolymer, tetrafluoroethylene-propylene copolymer, etc. In practice it is generally to keep the polyol-vulcanizable fluororubber that are commercially available.
- (A) Component Polyol As the (E) component polyol-based vulcanizing agent used as a vulcanizing agent for a vulcanizable fluororubber, for example, 2,2-bis (4-hydroxyphenyl) propane [bisnol A], 2, 2-Bis (4-hydroxyphenyl) perfluoropropane [bisphenol AF], bis (4-hydroxyphenyl) sulfone [bisphenol S], 2,2-bis (4-hydroxyphenyl) methane [bisphenol F], bisphenol A- Bis (diphenyl phosphate), 4,4'-dihydroxydiphenyl, 2,2-bis (4-hydroxyphenyl) butane and the like can be mentioned, and preferably bisphenol A, bisphenol AF and the like are used.
- polyol type vulcanizing agents are generally used in a proportion of about 0.5 to 8 parts by weight, preferably about 2 to 6 parts by weight, per 100 parts by weight of the polyol vulcanizable fluororubber.
- group vulcanizing agent is also used as a masterbatch with fluororubber.
- a quaternary onium salt which is a quaternary phosphonium salt or a quaternary ammonium salt is used, and preferably a quaternary phosphonium salt is used.
- These quaternary onium salts are used in a proportion of about 0.5 to 6 parts by weight, preferably about 1 to 4 parts by weight, per 100 parts by weight of the polyol vulcanizable fluororubber.
- the vulcanization accelerator is also used as a masterbatch with a fluororubber.
- the quaternary phosphonium salt is a compound represented by the following general formula.
- [PR 1 R 2 R 3 R 4] + X - R 1 to R 4 each represent an alkyl group having 1 to 25 carbon atoms, an alkoxyl group, an aryl group, an alkylaryl group, an aralkyl group or a polyoxyalkylene group, or two or three of them together with P have a multiple ring structure it is also possible to form X -: Cl -, Br - , I -, HSO 4 -, H 2 PO 4 -, RCOO -, ROSO 2 -, CO 3 - - anionic specifically such, tetraphenylphosphonium chloride , Benzyltriphenylphosphonium bromide, benzyltriphenylphosphonium chloride, triphenylmethoxymethylphosphonium chloride, triphenylmethylcarbonylmethylphosphonium chloride, triphenylethoxycarbonylmethyl
- the quaternary ammonium salt has a general formula [NR 1 R 2 R 3 R 4 ] + X ⁇ (Wherein R 1 to R 4 and X - are the same as above), for example 1-alkylpyridinium salt, 5-aralkyl-1,5-diazabicyclo [4,3,0] -5- Nonenium salts, 8-aralkyl-1,8-diazabicyclo [5,4,0] -7-undecenium salts and the like are used.
- the soil-like graphite of the component (B) is obtained from a coal bed in sedimentary rock, etc., has lubricity like other graphites, and is excellent in wear resistance. In addition, compared with scale-like graphite etc., it has less delamination, is excellent in non-sticking property, and is excellent in post-sealability and compression resistance.
- the earthy graphite is used in a proportion of about 10 to 50 parts by weight, preferably about 25 to 40 parts by weight, per 100 parts by weight of the polyol vulcanizable fluororubber. If it is used at an addition ratio lower than this, it will be inferior in non-stickiness and abrasion resistance, and if it is used at an addition ratio higher than this, it will be inferior to compression resistance and abrasion resistance.
- the earthy graphite one having a maximum particle diameter of 45 ⁇ m or less and an average particle diameter of 20 ⁇ m or less is used, and when graphite other than earthy graphite is used, the average particle diameter is of the same grade.
- the dispersion particle size of the rubber solution is increased, and problems occur in sealability and compression resistance.
- a novolak type phenol resin derived from p-substituted phenol, a resol type phenol resin, an epoxy-modified phenol resin, etc. is about 1 to 10 weight per 100 weight parts of polyol vulcanizable fluororubber It is used in a proportion of preferably about 3 to 6 parts by weight. If the proportion of phenolic resin added is less than this, oil resistance and air heat aging resistance will be poor, while if it is used at more than this proportion, abrasion resistance and air heat aging resistance will be poor. become.
- phenolic resins used are given below.
- Examples of the silane coupling agent of the component (D) include ⁇ -aminopropyltriethoxysilane, ⁇ -aminopropyltrimethoxysilane, N- ⁇ - (aminoethyl) - ⁇ -aminopropyltriethoxysilane, N- ⁇ - At least one of amino group-containing alkoxysilanes such as (aminoethyl) - ⁇ -aminopropyltrimethoxysilane, and vinyl group-containing alkoxysilanes such as vinyltriethoxysilane and vinyltrimethoxysilane is preferably used.
- silane coupling agents are used in a proportion of about 1 to 4 parts by weight, preferably about 2 to 3 parts by weight, in terms of solid content, per 100 parts by weight of the polyol-vulcanizable fluororubber. If the addition ratio of the silane coupling agent is less than this, compression resistance and air heat aging resistance will be inferior, while if it is used at more than this addition, not only the pot life will be significantly reduced, but also the antifreeze liquid And resistance to air-heating resistance.
- various fillers such as carbon black, silica, titanium oxide, alumina, iron oxide, clay, calcium carbonate, PTFE powder, etc. are blended and used, and reinforcing properties From the aspect of carbon black, preferably MT carbon black or silica is used.
- oxides or hydroxides of divalent metals such as magnesium oxide, zinc oxide, calcium oxide and calcium hydroxide, and further basic magnesium, aluminum, hydroxycarbonate hydrate (hydrotalcite), etc. are acid acceptors. Used as
- the preparation of the fluororubber composition appropriately blended with the necessary compounding agents is carried out by kneading using a closed-type kneader such as an intermix, a kneader, a Banbury mixer or an open roll.
- a closed-type kneader such as an intermix, a kneader, a Banbury mixer or an open roll.
- a hydrocarbon wax, a silicone wax, or the like may be added as a processing aid and used.
- a fluororubber composition is generally used as a one-component coating agent.
- the fluororubber coating solution is dissolved or dispersed using a general rotary stirrer or a high shear type dispersing machine such as a homogenizer or a ball mill, and then a solid content concentration is about 20 to 20 using a triple roll or the like. It is prepared as an organic solvent solution adjusted to 60% by weight, preferably about 25 to 50% by weight. At this time, if necessary, a commercially available silicone antifoaming agent may be added and used.
- Organic solvents used to form the fluororubber coating solution which is a one-component coating agent include ketones such as methyl ethyl ketone, 2-butanone, di-n-propyl ketone, diisobutyl ketone, pholone, isophorone, cyclohexanone or methanol Alcohols such as ethanol, isopropanol, n-butanol, amyl alcohol, heptanol and the like are preferably used, and may be a ketone-alcohol mixed solvent.
- ketones such as methyl ethyl ketone, 2-butanone, di-n-propyl ketone, diisobutyl ketone, pholone, isophorone, cyclohexanone or methanol
- Alcohols such as ethanol, isopropanol, n-butanol, amyl alcohol, heptanol and the like are preferably used, and may be
- the organic solvent solution of the fluororubber composition thus prepared can be treated with a chromate treatment or a chromate treatment alternative by using a knife coater, flow coater, roll coater or the like as a one-component coating agent, or by screen printing.
- the uncoated metal sheet is coated directly with an arbitrary thickness, preferably about 10 to 100 ⁇ m, preferably about 20 to 30 ⁇ m after drying, and dried. Oven curing is carried out under conditions of ⁇ 230 ° C. for about 2 to 30 minutes to form a fluororubber metal laminate.
- lubricating components such as graphite, PTFE, molybdenum dioxide, carbon black, paraffin wax and the like are main components, and as a binder, cellulose resin, acrylic resin, polybutadiene resin, urethane resin, etc. as a binder Is added, and a dispersion dispersed in water or an organic solvent such as toluene is applied to form a non-adhesive layer with a thickness of about 1 to 10 ⁇ m, thereby preventing sticking and preventing sticking.
- Example 1 Among the above components, the vulcanization accelerator was removed, and after kneading with a pressure kneader, the rubber compound was discharged, and the vulcanization accelerator was mixed with an open roll to prepare a rubber composition.
- This rubber composition was dissolved in a methyl ethyl ketone-methanol (volume ratio 9: 1) mixed solvent to a solid content concentration of 25% by weight using a rotary stirrer to prepare a rubber solution.
- a flow coater this rubber solution is applied on a SUS301 metal plate (0.2 mm thick) that has not been subjected to surface treatment other than solvent degreasing so that the thickness after drying is 25 ⁇ m, and the solvent is dried. Then, the mixture was vulcanized at 220 ° C. for 3 minutes in an oven to obtain a fluororubber-laminated metal plate.
- Rubber residual ratio is 100% 4: Less than 100% of rubber residual ratio 95% or more 3: Less than 95% rubber residual ratio of 85% or more 2: Less than 85% rubber residual ratio of 65% or more 1: Less than 65% rubber residual ratio
- Antifreeze test The fluorine rubber metal laminate was immersed in water at 150 ° C. for 100 hours in a pressure-resistant container, and then a test was conducted and evaluated in the same manner as an air resistance heat aging test. After soaking the fluorine rubber metal laminate in IRM 903 oil at 200 ° C. for 15 hours, Fixing test (reworkability) that was tested and evaluated in the same way as air heat aging test.
- Example 2 In Example 1, the amount of earthy graphite was changed to 10 parts by weight.
- Example 3 In Example 1, the amount of earthy graphite was changed to 50 parts by weight.
- Example 4 In Example 1, the amount of silane coupling agent was changed to 1 part by weight (in terms of solid content).
- Example 5 In Example 1, the amount of silane coupling agent was changed to 4 parts by weight (in terms of solid content).
- Example 6 In Example 1, the amount of epoxy-modified phenolic resin was changed to 1 part by weight.
- Example 7 In Example 1, the amount of epoxy-modified phenolic resin was changed to 15 parts by weight.
- Example 1 Comparative Example 1 In Example 1, the same amount of scaly graphite (Nippon Carbon Co., Ltd. C-1, average particle diameter 11 ⁇ m) was used instead of the soil-like graphite.
- scaly graphite Natural Carbon Co., Ltd. C-1, average particle diameter 11 ⁇ m
- Comparative example 2 In Example 1, the same amount of scaly graphite (Nippon Graphite product HOP, average particle diameter 3 ⁇ m) was used instead of the earthy graphite.
- Comparative example 4 In Example 1, the amount of earthy graphite was changed to 100 parts by weight.
- Comparative example 7 In Example 1, no epoxy-modified phenolic resin was used.
- Comparative Example 8 In Example 1, the amount of epoxy-modified phenolic resin was changed to 30 parts by weight.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Laminated Bodies (AREA)
- Sealing Material Composition (AREA)
- Gasket Seals (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
(1) 一液性のコーティング剤として用いることにより、
・クロメート処理を行っていない金属板に適用されるため、Crフリーであ
る
・多層コーティングタイプではないため、VOC排出量が少なく、環境負荷が
小さい
・工程が煩雑ではないため、加工コストを下げることができる
(2) 土状黒鉛という特定のグラファイトを選択して用いることにより、
・ゴム溶液の粒度を20μm以下とすることが容易であるため、平滑で初期
シール性にすぐれている
・鱗片状黒鉛と比べ層間剥離が少なく、非固着性を有するため、リワーク
性にすぐれている
(3) フェノール樹脂とシランカップリング剤とを併用することにより、
・耐不凍液性や耐油性・耐熱性といった長期耐久性を得ることができる
〔PR1R2R3R4〕+X-
Rl~R4:炭素数1~25のアルキル基、アルコキシル基、アリール基、アル
キルアリール基、アラルキル基またはポリオキシアルキレン基
であり、あるいはこれらの内2~3個がPと共に複数環構造を形成
することもできる
X-:Cl-、Br-、I-、HSO4 -、H2PO4 -、RCOO-、ROSO2 -、CO3 - -等のアニオン
具体的には、テトラフェニルホスホニウムクロライド、ベンジルトリフェニルホスホニウムブロマイド、ベンジルトリフェニルホスホニウムクロライド、トリフェニルメトキシメチルホスホニウムクロライド、トリフェニルメチルカルボニルメチルホスホニウムクロライド、トリフェニルエトキシカルボニルメチルホスホニウムクロライド、トリオクチルベンジルホスホニウムクロライド、トリオクチルメチルホスホニウムクロライド、トリオクチルエチルホスホニウムアセテート、テトラオクチルホスホニウムクロライド、トリオクチルエチルホスホニウムジメチルホスフェートなどが用いられる。第4級ホスホニウム塩はまた、特許文献2に記載される如きポリヒドロキシ芳香族化合物等の活性水素含有芳香族化合物との等モル分子化合物であってもよい。
〔NR1R2R3R4〕+X-
(ここで、Rl~R4およびX-は上記と同じである)で表わされる化合物、例えば1-アルキルピリジニウム塩、5-アラルキル-1,5-ジアザビシクロ[4,3,0]-5-ノネニウム塩、8-アラルキル-l,8-ジアザビシクロ[5,4,0]-7-ウンデセニウム塩などが用いられる。
p-アルキル置換フェノールから導かれたノボラック型フェノール樹脂:
m:4~5
n:0.1程度
レゾール型フェノール樹脂:
R:水素原子、メチル基
n:1~6(平均)
エポキシ変性フェノール樹脂:
n:1~6(平均)
シール性(製品の表面平滑性):
フッ素ゴム金属積層板をガスケットとし、エア圧力0.15MPaを加えたと
き、リークしたエア量が5ml/分未満をシール性○、5~10ml未満/分を
シール性△、10ml/分以上をシール性×と評価
耐圧縮試験(ゴムのフロー性):
フッ素ゴム金属積層板に、150℃、2~4トン/cm2(196~392MPa)、5分間
の条件下で、ステンレス鋼製凸部を押付け、圧縮したときのゴムの流
れ出る状態を次の5段階で評価し、評価4以上を○、3を△、2以下
を×とした
5:金属露出なし、ゴム流れ殆どなし
4:金属露出なし、ゴム流れ 小
3:金属露出なし、ゴム流れ 中
(ゴム流れが少なからず生じているが、金属露出には至ってい
ない状態、すなわち金属露出が生ずる程のゴム流れが大きい
状態にはない)
2:金属露出 小、ゴム流れ 大
1:金属露出 大、ゴム流れ 大
耐空気加熱老化試験:
フッ素ゴム金属積層板を、ギヤ式オーブン中で200℃、72時間空気暴露
した後、ASTM D3002に対応するJIS K5400に準じてゴバン目試験を行い
、ゴムの剥離程度を次の5段階で評価し、評価4以上を○、3を△、
2以下を×とした
5:ゴム残存率が100%
4:ゴム残存率が100%未満95%以上
3:ゴム残存率が95%未満85%以上
2:ゴム残存率が85%未満65%以上
1:ゴム残存率が65%未満
耐不凍液試験:
フッ素ゴム金属積層板を、耐圧容器中で150℃の水中に100時間浸せき
した後、耐空気加熱老化試験と同様のゴバン目試験および評価を行っ
た
耐油試験:
フッ素ゴム金属積層板を、IRM903油中に200℃で15時間浸せきした後、
耐空気加熱老化試験と同様のゴバン目試験および評価を行った
固着試験(リワーク性):
耐圧縮試験と同様に、フッ素ゴム金属積層板に150℃、10分間という条
件下で面圧が0.5トン/cm2(49MPa)となるようにアルミニウム鋼製板を
押付け、冷却後に剥がした状態を評価し、アルミニウム鋼製板へのゴ
ムの固着率が10%未満を○、10~50%を△、50~100%(完全固着)を
×と評価
耐摩耗試験:
フッ素ゴム金属積層板について、ASTM D5963に対応するJIS K6264に準
拠するテーバー摩耗試験を実施し、摩耗容積が0.2ml未満を耐摩耗性○
、0.2~0.5mlを耐摩耗性△、0.5ml以上を×と評価
これらの各種試験で、○は非常にすぐれ、△は性能上問題がなく、×は性能上問題ありとされる。
実施例1において、土状黒鉛量を10重量部に変更した。
実施例1において、土状黒鉛量を50重量部に変更した。
実施例1において、シランカップリング剤量を1重量部(固形分換算)に変更した。
実施例1において、シランカップリング剤量を4重量部(固形分換算)に変更した。
実施例1において、エポキシ変性フェノール樹脂量を1重量部に変更した。
実施例1において、エポキシ変性フェノール樹脂量を15重量部に変更した。
実施例1において、土状黒鉛の代りに、同量の鱗片状黒鉛(日電カーボン製品C-1、平均粒径11μm)が用いられた。
実施例1において、土状黒鉛の代りに、同量の鱗状黒鉛(日本黒鉛製品HOP、平均粒径3μm)が用いられた。
実施例1において、土状黒鉛が用いられなかった。
実施例1において、土状黒鉛量を100重量部に変更した。
実施例1において、シランカップリング剤が用いられなかった。
実施例1において、シランカップリング剤量を16重量部(固形分換算)に変更した。
実施例1において、エポキシ変性型フェノール樹脂が用いられなかった。
実施例1において、エポキシ変性型フェノール樹脂量を30重量部に変更した。
Claims (9)
- (A)ポリオール加硫性フッ素ゴム100重量部当り、(B)土状黒鉛10~50重量部、(C)フェノール樹脂1~15重量部、(D)シランカップリング剤1~4重量部、(E)ポリオール系加硫剤0.5~8重量部および(F)加硫促進剤0.5~6重量部を含有せしめたフッ素ゴム組成物を金属板上に適用し、フッ素ゴム組成物を加硫して積層せしめたフッ素ゴム金属積層板。
- 金属板がクロメート処理またはクロメート代替処理を行わない金属板である請求項1記載のフッ素ゴム金属積層板。
- クロメート処理またはクロメート代替処理を行わない金属板が溶剤脱脂またはアルカリ脱脂した金属板である請求項2記載のフッ素ゴム金属積層板。
- フッ素ゴム組成物中の土状黒鉛が最大粒径が45μm以下であり、平均粒径が20μm以下である請求項1記載のフッ素ゴム金属積層板。
- フッ素ゴム組成物中のフェノール樹脂が、p-置換フェノールから導かれたノボラック型フェノール樹脂、レゾール型フェノール樹脂またはエポキシ変性フェノール樹脂である請求項1記載のフッ素ゴム金属積層板。
- フッ素ゴム組成物中のポリオール系加硫剤が、第4級ホスホニウム塩および第4級アンモニウム塩から選ばれた4級オニウム塩である請求項1記載のフッ素ゴム金属積層板。
- フッ素ゴム組成物が一液性コーティング剤として用いられた請求項1記載のフッ素ゴム金属積層板。
- 固形分濃度が20~60重量%の一液性コーティング剤が用いられた請求項7記載のフッ素ゴム金属積層板。
- 加硫フッ素ゴム層上に非粘着層を形成させた請求項1記載のフッ素ゴム金属積層板。
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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US13/058,902 US8475917B2 (en) | 2008-09-09 | 2009-08-27 | Fluororubber-metal laminate sheet |
CN200980135198.1A CN102149539B (zh) | 2008-09-09 | 2009-08-27 | 氟橡胶金属层叠板 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP2008-230514 | 2008-09-09 | ||
JP2008230514A JP5407233B2 (ja) | 2008-09-09 | 2008-09-09 | フッ素ゴム金属積層板 |
Publications (1)
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WO2010029851A1 true WO2010029851A1 (ja) | 2010-03-18 |
Family
ID=42005110
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Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2009/064905 WO2010029851A1 (ja) | 2008-09-09 | 2009-08-27 | フッ素ゴム金属積層板 |
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Country | Link |
---|---|
US (1) | US8475917B2 (ja) |
JP (1) | JP5407233B2 (ja) |
KR (1) | KR101641590B1 (ja) |
CN (1) | CN102149539B (ja) |
WO (1) | WO2010029851A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011102296A1 (ja) | 2010-02-22 | 2011-08-25 | Nok株式会社 | フッ素ゴム金属積層板 |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103057238B (zh) * | 2011-10-20 | 2015-07-01 | 岱山县威尔密封件有限公司 | 一种密封垫片的制作方法 |
US9086150B2 (en) * | 2013-01-24 | 2015-07-21 | Federal-Mogul Corporation | Elastomeric shaft seal formed without oven post curing |
JP6302367B2 (ja) * | 2014-06-24 | 2018-03-28 | ニチアス株式会社 | コーティング剤 |
EP3715680A4 (en) * | 2017-11-24 | 2021-08-18 | Nok Corporation | SEALING MATERIAL |
CN114746520B (zh) * | 2019-12-06 | 2023-06-06 | Nok株式会社 | 涂布液和使用该涂布液的氟橡胶金属层叠板 |
JP7012063B2 (ja) * | 2019-12-11 | 2022-01-27 | 三菱電線工業株式会社 | 半導体製造装置用シール材 |
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JP4168480B2 (ja) * | 1998-02-27 | 2008-10-22 | ダイキン工業株式会社 | フッ素ゴム水性塗料組成物および被覆物品 |
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- 2009-08-27 CN CN200980135198.1A patent/CN102149539B/zh active Active
- 2009-08-27 US US13/058,902 patent/US8475917B2/en active Active
- 2009-08-27 WO PCT/JP2009/064905 patent/WO2010029851A1/ja active Application Filing
- 2009-08-27 KR KR1020117005878A patent/KR101641590B1/ko active IP Right Grant
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KR101641590B1 (ko) | 2016-07-21 |
JP2010064291A (ja) | 2010-03-25 |
CN102149539A (zh) | 2011-08-10 |
KR20110052710A (ko) | 2011-05-18 |
US8475917B2 (en) | 2013-07-02 |
US20110143124A1 (en) | 2011-06-16 |
CN102149539B (zh) | 2014-05-07 |
JP5407233B2 (ja) | 2014-02-05 |
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