WO2014017375A1 - フッ素樹脂製シールリング - Google Patents
フッ素樹脂製シールリング Download PDFInfo
- Publication number
- WO2014017375A1 WO2014017375A1 PCT/JP2013/069503 JP2013069503W WO2014017375A1 WO 2014017375 A1 WO2014017375 A1 WO 2014017375A1 JP 2013069503 W JP2013069503 W JP 2013069503W WO 2014017375 A1 WO2014017375 A1 WO 2014017375A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- ptfe resin
- seal ring
- plasma
- sealing ring
- ptfe
- Prior art date
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Classifications
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- 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
- F16J15/16—Sealings between relatively-moving surfaces
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- 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
- F16J15/16—Sealings between relatively-moving surfaces
- F16J15/32—Sealings between relatively-moving surfaces with elastic sealings, e.g. O-rings
- F16J15/3284—Sealings between relatively-moving surfaces with elastic sealings, e.g. O-rings characterised by their structure; Selection of materials
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C59/00—Surface shaping of articles, e.g. embossing; Apparatus therefor
- B29C59/14—Surface shaping of articles, e.g. embossing; Apparatus therefor by plasma treatment
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
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- 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
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- 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
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- 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
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/14—Glass
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- 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
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
- C09K3/1006—Materials in mouldable or extrudable form for sealing or packing joints or covers characterised by the chemical nature of one of its constituents
- C09K3/1009—Fluorinated polymers, e.g. PTFE
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C59/00—Surface shaping of articles, e.g. embossing; Apparatus therefor
- B29C59/14—Surface shaping of articles, e.g. embossing; Apparatus therefor by plasma treatment
- B29C2059/147—Low pressure plasma; Glow discharge plasma
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C59/00—Surface shaping of articles, e.g. embossing; Apparatus therefor
- B29C59/14—Surface shaping of articles, e.g. embossing; Apparatus therefor by plasma treatment
- B29C59/142—Surface shaping of articles, e.g. embossing; Apparatus therefor by plasma treatment of profiled articles, e.g. hollow or tubular articles
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use 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; Derivatives of such polymers
- C08J2327/02—Characterised by the use 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; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use 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; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08J2327/18—Homopolymers or copolymers of tetrafluoroethylene
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/12—Chemical modification
- C08J7/123—Treatment by wave energy or particle radiation
Definitions
- the present invention relates to a fluororesin seal ring. More specifically, the present invention relates to a fluororesin seal ring capable of preventing welding of fluororesin members.
- resin seal rings are used for rotation or reciprocation including hydraulic circuits such as an automatic transmission (A / T) and a continuously variable transmission (CVT) for automobiles.
- a / T automatic transmission
- CVT continuously variable transmission
- Such a resin seal ring is generally provided with an abutment portion which becomes a discontinuous portion in a part of the ring in order to ensure mounting property in an annular groove, sealing property under pressure and sliding property under normal pressure.
- a circumferential gap (abutment clearance) is slightly generated in the abutment portion.
- the present applicant has proposed a seal ring material in which fluorocarbon resin is filled with oil coke and carbon fiber in Patent Document 1.
- the seal ring manufactured from such a material has improved creep resistance, there is a possibility that the fluororesins may adhere to each other under conditions that generate frictional heat under pressure.
- An object of the present invention is to provide a PTFE resin seal ring that does not adhere to the surface of the joint portion that forms a discontinuous portion of the seal ring even after a constant load is applied at a high temperature. It is in.
- An object of the present invention is to provide a PTFE obtained by subjecting at least one surface of the abutment portion forming discontinuous portions of the seal ring to a plasma reforming treatment using a non-polymerizable gas under a pressure condition of 10 to 500 Pa during plasma irradiation. This is achieved by a resin seal ring.
- the PTFE resin seal ring according to the present invention is subjected to low-pressure plasma treatment on the abutment surface and the state of CF bonding on the surface portion is changed, after a constant load is applied at a high temperature, however, since there is no sticking at the joint, it has excellent effects such as ensuring sealing performance under pressure and sliding performance under normal pressure, such as an automatic transmission for automobiles (A / T) and continuously variable It is effectively used as a sealing material used for rotation or reciprocation including a hydraulic circuit such as a transmission (CVT).
- a / T automatic transmission for automobiles
- CVT transmission
- the seal ring can be used continuously over a wide temperature range, preferably -200 to + 260 ° C, has excellent heat resistance and cold resistance, and has a very low coefficient of friction of 0.04 to 0.3 and excellent friction resistance.
- PTFE resin is used.
- homo-PTFE can be used as PTFE, but it has been partially modified (several mol% or less) with a monomer containing a polyfluoroalkyl group such as fluoroalkyl vinyl ether or hexafluoropropylene or ethylene.
- PTFE can also be used.
- PTFE is known to contain various fillers and can be used for various applications. In the present invention, it varies depending on the type and properties of the filler, but generally about the total amount with PTFE.
- the filler can be used by adding 70% by weight or less, preferably about 1 to 30% by weight. Examples of the filler that can be contained in PTFE include the following, and two or more of these fillers can be used in combination.
- Glass fibers see Patent Documents 4 to 5 Generally, those having an average fiber diameter of about 1 to 50 ⁇ m, preferably about 5 to 15 ⁇ m, and an average fiber length of about 10 to 1000 ⁇ m, preferably about 50 to 200 ⁇ m are used. These glass fibers are preferably used after surface treatment with a silane coupling agent or the like in advance.
- Carbon fiber see Patent Document 1, 5-9, pitch type, rayon type, polyacrylonitrile type, etc., preferably pitch type, particularly preferably highly graphitized pitch type, generally average A fiber having a fiber diameter of about 1 to 50 ⁇ m, preferably about 5 to 20 ⁇ m, particularly preferably about 7 to 15 ⁇ m, and an average fiber length of about 10 to 1000 ⁇ m, preferably about 20 to 500 ⁇ m, particularly preferably about 50 to 200 ⁇ m is used. It is done.
- Ceramic fiber or ceramic powder see Patent Document 10 SiC, Al 2 O 3 , WC, Y 2 O 3 , MgO, SiO 2 , Si 3 N 4 , ZrO 2, etc.
- Graphite powder see Patent Documents 9, 11, and 15 Either natural graphite (such as earth, lump, powder) or artificial graphite can be used.
- the average particle diameter is generally 30 ⁇ m or less, although it depends on the properties.
- Coke See Patent Documents 1, 7-8, and 14 Coal coke, petroleum coke, etc., having an average particle size of about 1 to 200 ⁇ m, preferably 10 to 50 ⁇ m, particularly preferably about 3 to 30 ⁇ m Used.
- Carbon beads see Patent Document 8 and 12-13, preferably those obtained using an aromatic polymer as a raw material, and generally those having an average particle size of about 3 to 30 ⁇ m, preferably about 10 to 20 ⁇ m.
- Carbon black Ketjen black, thermal grade carbon black or the like having an arithmetic average particle size of about 70 to 90 nm is used.
- Bronze powder see Patent Documents 15 to 16 Cu alloy containing 2 to 35% by weight of Sn, for example, Cu 85 to 98% by weight, preferably 88 to 92% by weight, Sn 2 to 15% by weight, preferably Those having a composition of 8 to 12% by weight, or those having a Cu to Cr ratio of approximately 9: 1 and an average particle size of approximately 10 to 50 ⁇ m are generally used.
- the plasma reforming process is performed on at least one surface of the sealing ring joint using a low-pressure plasma apparatus. Specifically, it is placed in a vacuum chamber so that the abutment surface of the seal ring does not match, and the chamber (vacuum tank) is evacuated to a predetermined degree of vacuum, generally 5 to 100 Pa or less, and then non-polymerized This is performed by introducing a sex gas and applying a predetermined power for a predetermined time using a high-frequency power source having a predetermined frequency.
- the abutment portion of the seal ring is a discontinuous portion provided in a part of the ring, and this surface refers to the opposite surface in the abutment portion, and the shape thereof is a straight cut, stepped shape.
- straight cuts include those described in Patent Document 1
- examples of special step cuts include those described in Patent Documents 2 to 3.
- the low-pressure plasma apparatus for example, an apparatus in which a lower electrode and an upper electrode are positioned so as to face each other in a vacuum chamber and at least one of the electrodes is connected to a high-frequency power source or a microwave power source is used.
- the inside of the system is depressurized to 5 to 100 Pa or less by a vacuum pump, and then a non-reactive gas such as argon, helium, nitrogen, or a non-polymerizable gas such as oxygen is introduced.
- a non-reactive gas such as argon, helium, nitrogen, or a non-polymerizable gas such as oxygen is introduced.
- the pressure in the vacuum chamber is 10 to 500 Pa, preferably 20 to 100 Pa.
- a high frequency power source such as a frequency of 40 kHz or 13.56 MHz or a microwave power source of a frequency of 2.45 GHz
- a power of about 10 to 30000 W is applied for 1 to 30 minutes. Done by supplying.
- the surface structure of polytetrafluoroethylene is modified and surface etching is performed.
- conditions other than pressure that is, the type of gas used, the power source plasma excitation electric field frequency, the power, the temperature condition during irradiation, and the irradiation time are not particularly limited.
- plasma irradiation is performed under a pressure other than the above, plasma is not stably generated.
- the plasma irradiation treatment is applied only to the abutment surface having various shapes with the seal ring open so that the plasma irradiation treatment is applied to at least one of the opposite surfaces of the abutment portion of the seal ring. Is called.
- Patent Document 17 a surface modification method is disclosed in which a molded product containing a fluororesin as a main component is subjected to a plasma irradiation treatment under a pressure of 1.5 to 25 Pa. It is said that the object can be firmly bonded to other members, and there is no technical idea for preventing the fluororesin members from sticking to each other.
- Example 1 After mixing 68% by weight of PTFE (Asahi Glass Product G163), 30% by weight of glass fiber (Nitto Boseki CCS-3J-451S) and 2% by weight of oil coke (Chuetsu Graphite Industrial Products; average particle size 20 ⁇ m) using a mixer Then, it was compression-molded at 10 to 20 MPa by a compression molding machine and then fired at a melting point or higher in a firing furnace to produce a rectangular parallelepiped (4 ⁇ 4 ⁇ 4 mm) test piece.
- PTFE Adahi Glass Product G163
- glass fiber Nito Boseki CCS-3J-451S
- oil coke Choketsu Graphite Industrial Products; average particle size 20 ⁇ m
- the obtained test piece was left on the lower electrode in the vacuum chamber of the low-pressure plasma processing apparatus, and the inside of the vacuum chamber was evacuated until the degree of vacuum became 10 Pa.
- argon gas is introduced, and while maintaining the pressure in the vacuum chamber at about 60 Pa, 200 W of power is supplied to the upper electrode from a high frequency power supply with a frequency of 13.56 MHz for 5 minutes, and argon gas is plasma
- the PTFE surface was modified.
- the gas supply unit and the gas exhaust apparatus are disposed so that the upper electrode and the lower electrode are opposed to the upper side and the lower side of the vacuum chamber provided on the outer side surface, respectively, What was connected with the high frequency electric power source arrange
- Adhesion resistance evaluation A PTFE surface (4 ⁇ 4mm) treated with plasma modification and PTFE surface not treated with plasma (4 ⁇ 4mm) of the test piece are overlapped and sandwiched between jigs, then room temperature Apply a slight vibration at a frequency of 200Hz for 30 seconds while applying a surface pressure of 3MPa under the conditions, remove the jig, pull it perpendicular to the adhesive surface, and measure the bond strength with an autograph.
- the surface pressure is 7 MPa. Hold at 160 ° C for 1 hour while applying load, remove the jig after cooling, pull perpendicular to the adhesive surface, and measure the adhesive strength with an autograph
- Example 2 In Example 1, two types of sticking resistance evaluations were performed using a test piece in which PTFE surfaces subjected to plasma modification treatment were sandwiched between overlapping jigs.
- Example 3 In Example 1, two types of sticking resistance evaluations were performed on the plasma reforming process performed by changing the supply time of the high frequency power to 10 minutes.
- Example 4 In Example 3, two types of sticking resistance evaluations were performed using a test piece in which PTFE surfaces subjected to plasma modification treatment were sandwiched between overlapping jigs.
- Example 5 In Example 1, two types of sticking resistance evaluations were performed on the plasma reforming process performed by changing the supply time of the high frequency power to 20 minutes.
- Example 6 In Example 5, two types of sticking resistance evaluations were performed using a test piece in which PTFE surfaces subjected to plasma modification treatment were sandwiched between overlapping jigs.
- Example 7 In Example 1, two types of sticking resistance evaluations were performed on the plasma modified treatment using nitrogen gas instead of argon gas.
- Example 8 In Example 2, two types of sticking resistance evaluations were performed using a test piece in which PTFE surfaces subjected to plasma modification treatment were sandwiched between overlapping jigs.
- Comparative Example 1 In the sticking resistance evaluation of Example 1, two types of sticking resistance evaluations were performed using a surface in which surfaces not subjected to plasma modification treatment were sandwiched between overlapping jigs.
- Examples 9 to 16 and Comparative Example 2 In Examples 1 to 8 and Comparative Example 1, the PTFE amount was changed to 70% by weight and the oil coke amount was changed to 30% by weight, and no glass fiber was used. The results obtained are shown in Table 2 below.
- Examples 17 to 24, Comparative Example 3 In Examples 1 to 8 and Comparative Example 1, the PTFE amount was changed to 67% by weight, the oil coke amount was changed to 3% by weight, and the same amount of carbon black (Mitsubishi Chemical Ketjen Black ECP600JD) was used instead of glass fiber. (30% by weight) was used. The results obtained are shown in Table 3 below.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Plasma & Fusion (AREA)
- Gasket Seals (AREA)
- Sealing Material Composition (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sealing Devices (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
Abstract
Description
ガラス繊維:特許文献4~5参照
一般に、平均繊維径が約1~50μm、好ましくは約5~15μm、平均繊維長が約10~1000μm、好ましくは約50~200μmのものが用いられる。これらのガラス繊維は、予めシランカップリング剤等によって表面処理された上で用いられることが好ましい。
炭素繊維:特許文献1、同5~9参照
ピッチ系、レーヨン系、ポリアクリロニトリル系のものなどであって、好ましくはピッチ系、特に好ましくは高黒鉛化ピッチ系のものであって、一般にその平均繊維径が約1~50μm、好ましくは約5~20μm、特に好ましくは約7~15μm、平均繊維長が約10~1000μm、好ましくは約20~500μm、特に好ましくは約50~200μmのものが用いられる。
セラミックス繊維またはセラミックス粉末:特許文献10参照
SiC、Al2O3、WC、Y2O3、MgO、SiO2、Si3N4、ZrO2等の繊維または粉末であって、一般にその平均粒径が約0.4~100μm、好ましくは約0.7~30μmのものが用いられる。
黒鉛粉末:特許文献9、同11、同15参照
天然黒鉛(土状、塊状、粉末状など)あるいは人造黒鉛のいずれをも用いることができる。その平均粒径は、その性状にもよるが、一般には30μm以下のものが用いられる。
コークス:特許文献1、同7~8、同14参照
石炭コークス、石油コークス等であって、その平均粒径が約1~200μm、好ましくは10~50μm、特に好ましくは約3~30μmのものが用いられる。
カーボンビーズ:特許文献8、同12~13参照
好ましくは芳香族ポリマーを原料として得られるものが用いられ、一般にその平均粒径が約3~30μm、好ましくは約10~20μmのものが用いられる。
カーボンブラック:
算術平均粒径が約70~90nmのケッチェンブラック、サーマル級カーボンブラック等が用いられる。
ブロンズ粉末:特許文献15~16参照
Cuに2~35重量%のSnを加えた合金であり、例えばCu 85~98重量%、好ましくは88~92重量%、Sn 2~15重量%、好ましくは8~12重量%の組成を有するもの、あるいはCuとCrとの比がほぼ9:1で、一般には平均粒径が約10~50μmのものが用いられる。
PTFE(旭硝子製品G163)68重量%、ガラス繊維(日東紡績製品CSX-3J-451S)30重量%およびオイルコークス(中越黒鉛工業製品;平均粒径20μm)2重量%をミキサを用いて混合した後、圧縮成形機によって10~20MPaで圧縮成形され、次いで焼成炉中で融点以上にて焼成し、直方体形状(4×4×4mm)の試験片を作製した。
耐固着性評価A:試験片のプラズマ改質処理されたPTFE面(4×4mm)とプラズマ改質処理されていないPTFE面(4×4mm)とを重ね合わせて治具で挟んだ後、室温条件下で面圧3MPaの荷重をかけながら200Hzの周波数で微振動を30秒間与え、治具をはずしたうえで接着面に対して垂直に引張り、固着強度をオートグラフにて測定
耐固着性評価B:試験片のプラズマ改質処理された上記PTFE面とプラズマ改質処理されていない上記PTFE面とをそれぞれの両端部を上記長さで重ね合わせて治具で挟んだ後、面圧7MPaの荷重をかけながら160℃で1時間保持し、冷却後に治具をはずしたうえで接着面に対して垂直に引張り、固着強度をオートグラフにて測定
実施例1において、試験片のプラズマ改質処理されたPTFE面同士を重ね合わせ治具で挟んだものを用いて、2種類の耐固着性評価が行われた。
実施例1において、高周波電力の供給時間が10分間に変更されてプラズマ改質処理が行われたものについて、2種類の耐固着性評価が行われた。
実施例3において、試験片のプラズマ改質処理されたPTFE面同士を重ね合わせ治具で挟んだものを用いて、2種類の耐固着性評価が行われた。
実施例1において、高周波電力の供給時間が20分間に変更されてプラズマ改質処理が行われたものについて、2種類の耐固着性評価が行われた。
実施例5において、試験片のプラズマ改質処理されたPTFE面同士を重ね合わせ治具で挟んだものを用いて、2種類の耐固着性評価が行われた。
実施例1において、アルゴンガスの代わりに窒素ガスを用いてプラズマ改質処理が行われたものについて、2種類の耐固着性評価が行われた。
において、試験片のプラズマ改質処理されたPTFE面同士を重ね合わせ治具で挟んだものを用いて、2種類の耐固着性評価が行われた。
実施例1の耐固着性評価において、いずれも表面がプラズマ改質処理されていない面同士を重ね合わせ治具で挟んだものを用いて、2種類の耐固着性評価が行われた。
Claims (4)
- シールリングの不連続箇所を形成する合口部の少なくとも一方の面を、プラズマ照射時の圧力条件を10~500Paとし、非重合性ガスを用いてプラズマ改質処理したPTFE樹脂製シールリング。
- 非重合性ガスがアルゴン、ヘリウム、窒素または酸素である請求項1記載のPTFE樹脂製シールリング。
- PTFE樹脂が充填剤含有PTFE樹脂である請求項1記載のPTFE樹脂製シールリング。
- 充填剤含有PTFE樹脂が、ガラス繊維、炭素繊維、セラミックス繊維、セラミックス粉末、黒鉛粉末、コークス粉末、カーボンビーズ、カーボンブラックまたはブロンズ粉末を含有したPTFE樹脂である請求項3記載のPTFE樹脂製シールリング。
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
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EP13822957.0A EP2886913A4 (en) | 2012-07-25 | 2013-07-18 | FLUOR RESIN SEAL RING |
CN201380039279.8A CN104508334B (zh) | 2012-07-25 | 2013-07-18 | 氟树脂制密封环 |
US14/416,245 US20150184749A1 (en) | 2012-07-25 | 2013-07-18 | Fluororesin seal ring |
JP2013540931A JP5418743B1 (ja) | 2012-07-25 | 2013-07-18 | フッ素樹脂製シールリング |
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EP (1) | EP2886913A4 (ja) |
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Cited By (2)
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WO2016208648A1 (ja) * | 2015-06-24 | 2016-12-29 | コスモ石油株式会社 | 樹脂配合物 |
JP2019026664A (ja) * | 2017-07-26 | 2019-02-21 | Nok株式会社 | ポリテトラフルオロエチレン配合物、シール部材及び摺動部材 |
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CN107864663A (zh) * | 2015-07-28 | 2018-03-30 | 美国圣戈班性能塑料公司 | 密封件 |
JP6651017B2 (ja) * | 2017-02-16 | 2020-02-19 | Nok株式会社 | シール材 |
JP6607231B2 (ja) * | 2017-05-29 | 2019-11-20 | 株式会社オートネットワーク技術研究所 | リアクトル |
CN108758725B (zh) * | 2018-04-25 | 2022-06-21 | 曾文洲 | 耐高温密封弹性条、限排废气烟道结构、炉灶防水结构及炉灶 |
CN112639015B (zh) * | 2018-07-23 | 2022-09-23 | 旭硝子化学美国有限公司 | 玻璃纤维增强的含氟聚合物组合物 |
CN110079037B (zh) * | 2019-04-26 | 2021-09-24 | 广东欧特派环保材料科技有限公司 | 一种自润滑耐磨ptfe复合材料及其制备方法 |
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Also Published As
Publication number | Publication date |
---|---|
EP2886913A1 (en) | 2015-06-24 |
CN104508334A (zh) | 2015-04-08 |
US20150184749A1 (en) | 2015-07-02 |
JP5418743B1 (ja) | 2014-02-19 |
EP2886913A4 (en) | 2016-06-01 |
JPWO2014017375A1 (ja) | 2016-07-11 |
CN104508334B (zh) | 2017-07-11 |
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