JP4777389B2 - Fluororesin sheet with gasket filler and gasket - Google Patents
Fluororesin sheet with gasket filler and gasket Download PDFInfo
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- JP4777389B2 JP4777389B2 JP2008152764A JP2008152764A JP4777389B2 JP 4777389 B2 JP4777389 B2 JP 4777389B2 JP 2008152764 A JP2008152764 A JP 2008152764A JP 2008152764 A JP2008152764 A JP 2008152764A JP 4777389 B2 JP4777389 B2 JP 4777389B2
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- 239000000945 filler Substances 0.000 title claims description 33
- 238000005096 rolling process Methods 0.000 claims description 42
- 239000006057 Non-nutritive feed additive Substances 0.000 claims description 39
- 238000004519 manufacturing process Methods 0.000 claims description 16
- 239000002904 solvent Substances 0.000 claims description 16
- 238000004508 fractional distillation Methods 0.000 claims description 12
- 239000003209 petroleum derivative Substances 0.000 claims description 11
- 239000011342 resin composition Substances 0.000 claims description 10
- 229920005989 resin Polymers 0.000 claims description 9
- 239000011347 resin Substances 0.000 claims description 9
- 238000012360 testing method Methods 0.000 claims description 7
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 3
- 229910001873 dinitrogen Inorganic materials 0.000 claims description 3
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 12
- 238000011049 filling Methods 0.000 description 11
- 238000000034 method Methods 0.000 description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 238000005194 fractionation Methods 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 239000004810 polytetrafluoroethylene Substances 0.000 description 5
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000003566 sealing material Substances 0.000 description 4
- CNPVJWYWYZMPDS-UHFFFAOYSA-N 2-methyldecane Chemical compound CCCCCCCCC(C)C CNPVJWYWYZMPDS-UHFFFAOYSA-N 0.000 description 3
- 238000000280 densification Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- 239000011256 inorganic filler Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 0.000 description 2
- 235000012438 extruded product Nutrition 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 239000002657 fibrous material Substances 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 229910021393 carbon nanotube Inorganic materials 0.000 description 1
- 239000002041 carbon nanotube Substances 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 1
- 239000005023 polychlorotrifluoroethylene (PCTFE) polymer Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000003746 surface roughness Effects 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
Landscapes
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Description
本発明は、充填材入りフッ素樹脂シートの製造方法および充填材入りフッ素樹脂シートに関し、さらに詳しくはシール材などとして用いられる充填材入りフッ素樹脂シートの製造方法および充填材入りフッ素樹脂シートに関する。 The present invention relates to a method for producing a filled fluororesin sheet and a filled fluororesin sheet, and more particularly to a method for producing a filled fluororesin sheet used as a sealing material and the like and a filled fluororesin sheet.
充填材入りフッ素樹脂シートは、フッ素樹脂に充填材を充填してシート状に加工したものであり、フッ素樹脂の持つ耐薬品性、耐熱性、非粘着性、低摩擦性に加えて、充填材の持つ固有の機能・特性を付加し、あるいはフッ素樹脂の欠点である、耐摩耗性や対クリープ性を改善することにより、シール材等に多く用いられている。 Filled fluororesin sheet is a sheet made by filling fluororesin with a filler. In addition to the chemical resistance, heat resistance, non-adhesiveness, and low friction properties of fluororesin, It is often used for sealing materials by adding the unique functions and characteristics of, or improving the wear resistance and creep resistance, which are disadvantages of fluororesins.
シール材としては、フッ素樹脂に金属、黒鉛、無機充填材等を充填させて熱伝導率、耐摩耗性、クリープ特性等を向上させたものがあり、シート状ガスケットやグランドパッキンの編糸等に使用されている。 Sealing materials include fluorine resin filled with metal, graphite, inorganic filler, etc. to improve thermal conductivity, wear resistance, creep properties, etc. in use.
米国特許第3315020号明細書(特許文献1)には、PTFEと充填材と加工助剤との混合物を押出成形した後に1対の圧延ロールを一度、あるいは複数度通過させ圧延して長尺シートを得る技術が開示されている。しかしこの技術を利用して充填材入りフッ素樹脂シートからなるシート状ガスケットを作成する場合、充填材の充填率を高くすると、応力緩和特性は優れる傾向にあるものの、気密性が低く、シール材として満足できるものが得られない。 In U.S. Pat. No. 3,315,020 (Patent Document 1), a long sheet is formed by extruding a mixture of PTFE, a filler and a processing aid and then passing a pair of rolling rolls once or a plurality of times. A technique for obtaining the above is disclosed. However, when creating a sheet-like gasket made of a fluororesin sheet with a filler using this technology, if the filling rate of the filler is increased, the stress relaxation property tends to be excellent, but the airtightness is low, and as a sealing material I can't get a satisfactory one.
一方、特開2004−323717号公報(特許文献2)には、フッ素樹脂、膨潤性鉱物、充填材および加工助剤を含む組成物を押出成形した後に圧延ロールを通過させてシート状に延伸してなる充填材入りフッ素樹脂シートが開示されている。この充填材入りフッ素樹脂シートは、フッ素樹脂の充填率が低く充填材の充填率が高い場合であっても、応力緩和率、引張り強さなどに優れている。
しかしながら、特許文献2に記載の充填材入りフッ素樹脂シートにおいては、硬く粒子状をなした無機系充填材同士の間を埋めるバインダーとしてのフッ素樹脂が不足する傾向にあるため、シール性能の点でさらなる改善の余地があることがわかった。 However, in the fluororesin sheet with a filler described in Patent Document 2, there is a tendency for the fluororesin as a binder to fill the space between hard and particulate inorganic fillers, so that in terms of sealing performance It turns out that there is room for further improvement.
本発明は、上記のような問題に鑑みてなされたものであり、フッ素樹脂の充填率が低く充填材の充填率が高い場合であっても、高い応力緩和性と高い気密性(シール性能)とが両立した充填材入りフッ素樹脂シートおよびその製造方法を提供することを目的とする。 The present invention has been made in view of the above problems. Even when the filling rate of the fluororesin is low and the filling rate of the filler is high, high stress relaxation property and high airtightness (seal performance). It is an object of the present invention to provide a filled fluororesin sheet and a method for producing the same.
本発明者らは鋭意研究した結果、充填材入りフッ素樹脂シート製造の際の圧延工程において、加工助剤を徐々に揮発させることによって、高い応力緩和性と高い気密性とを両立した充填材入りフッ素樹脂シートを製造できることを見出し、本発明を完成させた。 As a result of diligent research, the present inventors have found that a filling agent that achieves both high stress relaxation and high airtightness by gradually evaporating the processing aid in the rolling process in the production of the filled fluororesin sheet. It discovered that a fluororesin sheet could be manufactured and completed this invention.
本発明の充填材入りフッ素樹脂シートの製造方法は、
フッ素樹脂、充填材および加工助剤を含有するシート形成用樹脂組成物を、ロール温度を
40〜80℃として圧延する工程を含み、
該加工助剤が、分留温度が120℃以下である石油系炭化水素溶剤を30質量%以上(ただし、加工助剤重量を100質量%とする。)含んでなる
ことを特徴としている。
The manufacturing method of the filled fluororesin sheet of the present invention,
Including a step of rolling a sheet-forming resin composition containing a fluororesin, a filler and a processing aid at a roll temperature of 40 to 80 ° C.,
The processing aid is characterized by comprising 30% by mass or more of a petroleum hydrocarbon solvent having a fractional distillation temperature of 120 ° C. or less (provided that the weight of the processing aid is 100% by mass).
前記組成物中の前記フッ素樹脂と前記充填材との質量比は、フッ素樹脂:充填材=1:0.1〜2であることが好ましい。
前記組成物中には、前記加工助剤がフッ素樹脂と充填材との合計100重量部に対して5〜50重量部含まれることが好ましい。
The mass ratio of the fluororesin and the filler in the composition is preferably fluororesin: filler = 1: 0.1-2.
In the composition, the processing aid is preferably contained in an amount of 5 to 50 parts by weight with respect to a total of 100 parts by weight of the fluororesin and the filler.
本発明の製造方法は、前記圧延工程により調製された圧延シートをさらに圧延する工程を含むことが好ましい。
本発明の充填材入りフッ素樹脂シートは、上記した本発明の充填材入りフッ素樹脂シートの製造方法により製造されることを特徴としている。
The production method of the present invention preferably includes a step of further rolling the rolled sheet prepared by the rolling step.
The filled fluororesin sheet of the present invention is manufactured by the above-described method for manufacturing a filled fluororesin sheet of the present invention.
本発明の製造方法によれば、フッ素樹脂の充填率が低く充填材の充填率が高いにもかかわらず、高い応力緩和特性と高い気密特性とを両立した充填材入りフッ素樹脂シートを製造することができる。 According to the production method of the present invention, it is possible to produce a filled fluororesin sheet that achieves both high stress relaxation characteristics and high airtightness characteristics even though the filling ratio of the fluororesin is low and the filling ratio of the filler is high. Can do.
本発明の充填材入りフッ素樹脂シートの製造方法は、フッ素樹脂、充填材および加工助剤を含有するシート形成用樹脂組成物を、ロール温度を40〜80℃として圧延する工程を含み、該加工助剤が、分留温度が120℃以下である石油系炭化水素溶剤を30質量%以上(ただし、加工助剤重量を100質量%とする。)含んでなることを特徴としている。 The method for producing a filled fluororesin sheet according to the present invention includes a step of rolling a sheet forming resin composition containing a fluororesin, a filler and a processing aid at a roll temperature of 40 to 80 ° C. The auxiliary agent is characterized in that it comprises 30% by mass or more of a petroleum hydrocarbon solvent having a fractional distillation temperature of 120 ° C. or less (however, the weight of the processing auxiliary is 100% by mass).
[シート形成用樹脂組成物]
<フッ素樹脂>
フッ素樹脂としては、四フッ化エチレン樹脂(PTFE)の他、変性PTFE、フッ化ビニリデン樹脂(PVDF)、四フッ化エチレン−エチレン共重合樹脂(ETFE)、三フッ化塩化エチレン樹脂(PCTFE)、四フッ化エチレン−六フッ化プロピレンエチレン共重合樹脂(FEP)および四フッ化エチレン−パーフロロアルキル共重合樹脂(PFA)など、従来より公知のフッ素樹脂をいずれも好ましく用いることができる。これらの中でも、特に、乳化重合によって得られたPTFEを使用することが押出成形、圧延などを行う際の加工性の面で好ましい。
[Resin composition for sheet formation]
<Fluorine resin>
As fluororesin, besides tetrafluoroethylene resin (PTFE), modified PTFE, vinylidene fluoride resin (PVDF), tetrafluoroethylene-ethylene copolymer resin (ETFE), trifluorochloroethylene resin (PCTFE), Conventionally known fluororesins such as tetrafluoroethylene-hexafluoropropylene-ethylene copolymer resin (FEP) and tetrafluoroethylene-perfluoroalkyl copolymer resin (PFA) can be preferably used. Among these, it is particularly preferable to use PTFE obtained by emulsion polymerization in terms of workability when performing extrusion molding, rolling, or the like.
フッ素樹脂としては、粉末状のものをそのまま用いても良く、水にフッ樹脂微粒子を分散させたディスパージョンを用いても良い。ディスパージョンを用いた場合においては、フッ素樹脂ディスパージョンに適量の水、充填材、加工助剤などを加えて攪拌するだけで充填材入りフッ素樹脂シート形成用組成物を得ることができ、該組成物を用いることにより、より効率的に充填材入フッ素樹脂シートを得ることができる。 As the fluororesin, a powdery one may be used as it is, or a dispersion in which fluororesin fine particles are dispersed in water may be used. In the case of using a dispersion, a composition for forming a fluororesin sheet with a filler can be obtained simply by adding an appropriate amount of water, filler, processing aid, etc. to the fluororesin dispersion and stirring the composition. By using a thing, a filler-containing fluororesin sheet can be obtained more efficiently.
<充填材>
充填材としては、目的に応じて、黒鉛、カーボンブラック、膨張黒鉛、活性炭、カーボンナノチューブ等の炭素系充填材;タルク、マイカ、クレー、炭酸カルシウム、酸化マグネシウム、等の無機充填材;またはPPS等の樹脂の粉体;
等が用いられる。また、炭素繊維、アラミド繊維、ロックウール等からなる繊維材長10mm以下の繊維材を充填材として用いても良い。
<Filler>
As the filler, depending on the purpose, carbon-based fillers such as graphite, carbon black, expanded graphite, activated carbon, and carbon nanotubes; inorganic fillers such as talc, mica, clay, calcium carbonate, magnesium oxide; or PPS Resin powders of
Etc. are used. Moreover, you may use the fiber material which consists of carbon fiber, an aramid fiber, rock wool, etc. and whose fiber material length is 10 mm or less as a filler.
本発明によれば、フッ素樹脂の充填率が低く充填材の充填率が高い場合であっても、高い応力緩和性と高い気密性とが両立した充填材入りフッ素樹脂シートを製造することができ、前記フッ素樹脂と前記充填材との質量比は1:0.1〜2、好ましくは1:1〜1.8とすることができる。 According to the present invention, even when the filling rate of the fluororesin is low and the filling rate of the filling material is high, it is possible to produce a filled fluororesin sheet having both high stress relaxation properties and high airtightness. The mass ratio of the fluororesin and the filler can be 1: 0.1 to 2, preferably 1: 1 to 1.8.
<加工助剤>
前記フッ素樹脂シート形成用組成物中には、加工助剤が含まれる。
本発明で用いられる加工助剤は、分留温度が120℃以下である石油系炭化水素溶剤を30質量%以上、好ましくは50質量%以上含んでおり(ただし、加工助剤重量を100質量%とする。)、特に好ましくは、本質的に、分留温度が120℃以下である石油系炭化水素溶剤のみからなる。
<Processing aid>
The composition for forming a fluororesin sheet contains a processing aid.
The processing aid used in the present invention contains 30% by mass or more, preferably 50% by mass or more of a petroleum hydrocarbon solvent having a fractional distillation temperature of 120 ° C. or less (however, the weight of the processing aid is 100% by mass). Particularly preferably consists essentially of petroleum hydrocarbon solvents having a fractional distillation temperature of 120 ° C. or lower.
分留温度が120℃以下である石油系炭化水素溶剤としては、代表例としてパラフィン系溶剤などが挙げられ、市販品であれば、たとえばアイソパーC(炭化水素系有機溶剤、分留温度:97〜104℃、エクソンモービル(有))などが挙げられる。 As a petroleum-type hydrocarbon solvent whose fractionation temperature is 120 degrees C or less, a paraffin-type solvent etc. are mentioned as a typical example, If it is a commercial item, for example, Isopar C (hydrocarbon-type organic solvent, fractionation temperature: 97- 104 ° C., Exxon Mobil (existing)).
従来の充填材入フッ素樹脂シートの製造方法においては、加工助剤として、分留温度の高い(たとえば180〜250℃)石油系炭化水素溶剤を用いるのが一般的であった。このような加工助剤は、圧延作業中に溶剤が揮発せず安定した圧延作業が行えるという点で汎用的ではあるが、後述する圧延工程でロール温度を上昇させても揮発し難い。 In the conventional method for producing a fluororesin sheet with a filler, it is common to use a petroleum hydrocarbon solvent having a high fractionation temperature (for example, 180 to 250 ° C.) as a processing aid. Such a processing aid is general-purpose in that the solvent does not volatilize during the rolling operation and a stable rolling operation can be performed, but it is difficult to volatilize even if the roll temperature is increased in the rolling process described later.
加工助剤に含まれてもよい、分留温度が120℃以下である石油系炭化水素溶剤以外の成分としては、分留温度が120℃を超える石油系炭化水素溶剤などが挙げられる。分留温度が120℃を超える石油系炭化水素溶剤としては、市販品であればアイソパーG(炭化水素系有機溶剤、分留温度:158〜175℃、エクソンモービル(有))などが挙げられる。 Examples of components other than petroleum hydrocarbon solvents having a fractionation temperature of 120 ° C. or lower that may be included in the processing aid include petroleum hydrocarbon solvents having a fractionation temperature exceeding 120 ° C. Examples of petroleum hydrocarbon solvents having a fractional distillation temperature exceeding 120 ° C include Isopar G (hydrocarbon organic solvent, fractional distillation temperature: 158 to 175 ° C, Exxon Mobil (existing)).
この加工助剤は、シート形成用樹脂組成物中に、フッ素樹脂と充填材との合計100重量部に対して5〜50重量部、好ましくは10〜30重量部含まれることが望ましい。加工助剤がこのような量で含まれていると、後述する圧延工程の初期段階で、フッ素樹脂を充分に膨潤させることができる。 The processing aid is desirably contained in the sheet-forming resin composition in an amount of 5 to 50 parts by weight, preferably 10 to 30 parts by weight, based on 100 parts by weight of the fluororesin and the filler. When the processing aid is contained in such an amount, the fluororesin can be sufficiently swollen at the initial stage of the rolling process described later.
シート形成用樹脂組成物は、本質的には、上記したフッ素樹脂、充填材、加工助剤のみからなる。
これらの成分が含まれたフッ素樹脂シート形成用樹脂組成物を調製するには、上記各成分を任意の順序で一度に、あるいは少量ずつ複数回に分けて容器内に添加し、攪拌・混合等すればよい。
The resin composition for forming a sheet essentially consists of the above-described fluororesin, filler, and processing aid.
In order to prepare a resin composition for forming a fluororesin sheet containing these components, the above-mentioned components are added to the container at a time in an arbitrary order, or divided into a plurality of portions, and stirred, mixed, etc. do it.
[フッ素樹脂シートの製造方法]
一般的な充填材入りフッ素樹脂シートの製造方法は、撹拌工程、予備成形工程、圧延工程、乾燥工程、焼成工程をこの順序で含んでいる。
[Method for producing fluororesin sheet]
A general method for producing a filled fluororesin sheet includes a stirring step, a preforming step, a rolling step, a drying step, and a firing step in this order.
<撹拌工程>
撹拌工程では、上述のように、フッ素樹脂、充填材、加工助剤を任意の順序で撹拌、混合する。撹拌効率が悪い場合には、加工助剤を多く添加し、撹拌終了後に余分な加工助剤を濾過により除去しても良い。
<Stirring step>
In the stirring step, as described above, the fluororesin, the filler, and the processing aid are stirred and mixed in an arbitrary order. If the stirring efficiency is poor, a large amount of processing aid may be added and excess processing aid may be removed by filtration after stirring.
<予備成形工程>
予備成形工程では、前記フッ素樹脂シート形成用樹脂組成物を押出成形し、プレフォーム(押出成形物)を製造する。
<Preliminary molding process>
In the preforming step, the fluororesin sheet forming resin composition is extruded to produce a preform (extruded product).
押出成形物(プレフォーム)の形状は、特に限定されないが、その後のシート形成の効率、シート性状の均質性などを考慮すると、ロッド状またはリボン状が望ましい。
本発明の製造方法においては後述する圧延工程において加工助剤を徐々に揮発させるため、混合工程および予備成形工程は、温度を加工助剤が揮発しないよう、圧延工程におけるロール温度よりも低い温度下で行うことが好ましい。
The shape of the extruded product (preform) is not particularly limited, but a rod shape or a ribbon shape is desirable in consideration of efficiency of subsequent sheet formation, uniformity of sheet properties, and the like.
In the production method of the present invention, since the processing aid is gradually volatilized in the rolling step described later, the mixing step and the preforming step are performed at a temperature lower than the roll temperature in the rolling step so that the processing aid does not volatilize. It is preferable to carry out with.
<圧延工程>
予備成形工程に続く圧延工程では、プレフォームを、二軸ロールに代表される圧延ロール間を通過させてシート状に圧延、成形する。従来技術においては、圧延工程は非加熱下で、具体的には室温付近の10〜30℃程度の温度下で行われており、しかも加工助剤としては分留温度の高い(たとえば180〜250℃)石油系炭化水素溶剤が一般的に用いられていたため、この圧延工程では加工助剤はほとんど揮発することはなかった。
<Rolling process>
In the rolling process following the pre-forming process, the preform is rolled and formed into a sheet shape by passing between rolling rolls represented by a biaxial roll. In the prior art, the rolling process is performed without heating, specifically at a temperature of about 10 to 30 ° C. near room temperature, and the processing aid has a high fractional distillation temperature (for example, 180 to 250). C) Petroleum hydrocarbon solvent was generally used, so that the processing aid hardly volatilized in this rolling process.
この加工助剤は、フッ素樹脂を膨潤させ、繊維化し易くさせるために用いられる。撹拌工程、予備成形工程、圧延工程においてシート形成用樹脂組成物に付加される圧縮力、せん断力によって一部のフッ素樹脂が繊維化することにより、フッ素樹脂シートには、マトリクスの複雑化によるシート強度、応力緩和特性が付与される。しかし、圧延されるフッ素樹脂シートの内部でフッ素樹脂が膨潤していると、このシートは柔かく変形しやすいため、二軸ロール等による圧縮を受けても平面方向への変形が優先して起こってしまい、シート内部の緻密化は起こりにくいと考えられる。なお、シート内部の緻密化とは、溶剤の揮発により生じた組成物内部の空孔が圧延によって埋まることをいう。 This processing aid is used to swell the fluororesin and facilitate fiber formation. A part of the fluororesin is fiberized by the compressive force and shearing force applied to the sheet-forming resin composition in the stirring process, preforming process, and rolling process. Strength and stress relaxation properties are imparted. However, if the fluororesin is swollen inside the rolled fluororesin sheet, this sheet is soft and easily deformed, and therefore deformation in the plane direction takes precedence even when subjected to compression by a biaxial roll or the like. Therefore, it is considered that densification inside the sheet is unlikely to occur. In addition, the densification inside a sheet | seat means that the void | hole inside the composition produced by volatilization of the solvent is filled up by rolling.
本発明の製造方法においては、この圧延工程は、ロール温度を40〜80℃として行われ、しかも、分留温度が低い(120℃以下)石油系炭化水素溶剤を多く含む加工助剤が用いられるため、二軸ロール等による圧延を実施する間に、シート形成用樹脂組成物中の(プレフォーム中の)加工助剤が徐々に揮発、除去される。したがって、圧延工程の初期段階では、加工助剤が多く存在するためにフッ素樹脂を膨潤させ繊維化させることができ、しかも圧延工程の後期段階では、加工助材の残存量が少ないことから、加工助剤の揮発に基づくシート内部での新たな空孔の形成が少ないため、シートの平面方向への変形に優先させてシート内部の緻密化を進めることができると考えられる。 In the production method of the present invention, the rolling step is performed at a roll temperature of 40 to 80 ° C., and a processing aid containing a large amount of a petroleum hydrocarbon solvent having a low fractional distillation temperature (120 ° C. or lower) is used. Therefore, the processing aid (in the preform) in the sheet-forming resin composition is gradually volatilized and removed during rolling with a biaxial roll or the like. Therefore, since there are many processing aids in the initial stage of the rolling process, the fluororesin can be swollen and fiberized, and in the later stage of the rolling process, the remaining amount of processing aids is small, Since the formation of new pores inside the sheet based on the volatilization of the auxiliary agent is small, it is considered that the densification inside the sheet can be advanced in preference to the deformation in the plane direction of the sheet.
また、比較的高い温度下で圧延が行われるため、フッ素樹脂の硬度がやや低下し、フッ素樹脂シートをより緻密化しやすくなる。
一方、圧延工程を40℃よりも低い温度で行うと、加工助剤が揮発し難くなる傾向にある。また、80℃を越える温度で圧延を行うと、加工助剤が過度に揮発してしまい、圧延工程初期の時点で残存する加工助剤が少なくなるため、フッ素樹脂を充分に膨潤させ、繊維化させることができず、得られる充填材入りフッ素樹脂シートの強度が劣る傾向にある。また、組成物中の加工助剤が急激に気化することにより膨れ現象が生じ、充填材入りフッ素樹脂シートの気密性も低下する傾向にある。
In addition, since the rolling is performed at a relatively high temperature, the hardness of the fluororesin is slightly lowered, and the fluororesin sheet is easily densified.
On the other hand, when the rolling process is performed at a temperature lower than 40 ° C., the processing aid tends to be less volatile. In addition, if rolling is performed at a temperature exceeding 80 ° C., the processing aid is excessively volatilized, and the processing aid remaining at the initial stage of the rolling process is reduced. The strength of the obtained fluororesin sheet with a filler tends to be inferior. Further, the processing aid in the composition is rapidly vaporized to cause a swelling phenomenon, and the hermeticity of the filled fluororesin sheet tends to be lowered.
また、本発明の製造方法では、前記圧延工程により調製された圧延シートをさらに圧延する工程を含むこと、すなわち圧延工程を複数回繰り返すことが好ましい。圧延を繰り返すことにより、フッ素樹脂シート内部をさらに緻密化することができる。なお圧延工程を繰り返す場合には、圧延を繰り返すごとにロール間隔を狭くする。 Moreover, in the manufacturing method of this invention, it is preferable to include the process of further rolling the rolling sheet prepared by the said rolling process, ie, to repeat a rolling process in multiple times. By repeating rolling, the inside of the fluororesin sheet can be further densified. In addition, when repeating a rolling process, a roll space | interval is narrowed every time rolling is repeated.
二軸ロールにより前記プレフォームを圧延してシート形成する際には、たとえばロール間距離を0.5〜20mmにセットし、ロール表面移動速度(シート押出速度)を5〜50mm/秒としてプレフォームを圧延すればよい。 When forming the sheet by rolling the preform with a biaxial roll, for example, the distance between the rolls is set to 0.5 to 20 mm, and the roll surface moving speed (sheet extrusion speed) is set to 5 to 50 mm / second. Can be rolled.
<乾燥工程>
乾燥工程では、前記の圧延されたシートを常温で放置するか、フッ素樹脂の沸点以下の温度で加熱することにより、加工助剤を除去する。
<Drying process>
In the drying step, the processing aid is removed by leaving the rolled sheet at room temperature or heating it at a temperature below the boiling point of the fluororesin.
<焼成工程>
焼成工程では、乾燥後シートをフッ素樹脂の融点以上の温度で加熱、焼結させる。加熱温度としては、シート全体を均一に焼成する必要があることと、過度の高温ではフッ素系有害ガスが発生することとを考慮すると、フッ素樹脂の種類によっても多少異なるが、たとえば340〜370℃が適当である。
<Baking process>
In the firing step, the dried sheet is heated and sintered at a temperature equal to or higher than the melting point of the fluororesin. The heating temperature varies slightly depending on the type of the fluororesin, for example, 340 to 370 ° C., considering that the entire sheet needs to be uniformly fired and that a fluorine-based harmful gas is generated at an excessively high temperature. Is appropriate.
[充填材入りフッ素樹脂シート]
このような本発明の製造方法によって、充填材入りフッ素樹脂シートが製造される。この充填材入りフッ素樹脂シートは、応力緩和性と気密性とが共に高く、JIS R3453に準拠
した引張り強さは8MPa以上であり、かつ該シートから作成したφ48mm×φ67mm×厚さ1.5mmガスケット試験片に対して、面圧19.6MPa(200kgf/cm2G)、窒素ガス内圧0.98MPa(1.0kgf/cm2G)として気密試験を行った場合の漏洩量は9×10-5Pa・m3/s以下であり、好ま
しくは前記引張り強さは10MPa以上であり、かつ漏洩量は7×10-5Pa・m3/s以下である。
[Filled fluororesin sheet]
By such a production method of the present invention, a filled fluororesin sheet is produced. This filled fluororesin sheet has both high stress relaxation and air tightness, has a tensile strength of 8 MPa or more in accordance with JIS R3453, and has a φ48 mm × φ67 mm × 1.5 mm thickness gasket test made from the sheet. The leak rate is 9 × 10 -5 Pa · m 3 when the airtight test is performed on the piece with a surface pressure of 19.6 MPa (200 kgf / cm 2 G) and nitrogen gas internal pressure of 0.98 MPa (1.0 kgf / cm 2 G). The tensile strength is preferably 10 MPa or more, and the leakage amount is 7 × 10 −5 Pa · m 3 / s or less.
[実施例]
以下、本発明の製造方法を実施例によりさらに詳細に説明するが、本発明はこれらの実施例により何ら限定されるものではない。
[Example]
EXAMPLES Hereinafter, although the manufacturing method of this invention is demonstrated in detail by an Example, this invention is not limited at all by these Examples.
<試験方法>
厚さ1.5mmのシートから試験片を作成し、以下のように気密性および引張強度を測定し
た。
<Test method>
Test pieces were prepared from a sheet having a thickness of 1.5 mm, and hermeticity and tensile strength were measured as follows.
漏洩量(気密性);
φ48mm×φ67mmの寸法に打ち抜いたガスケット試験片を、φ100mm×高さ50mm、表
面粗さRmax=12μmの鋼フランジ間に装着し、圧縮試験機により面圧19.6MPa(200kgf/cm2G)となるよう荷重を負荷した。フランジに設けられた圧力導入用の貫通孔からガスケット内径側に窒素ガス内圧0.98MPa(1.0kgf/cm2G)を負荷した後圧力導入配管を封じ、1時間保持した。保持前後の圧力変化を圧力センサで読み取り、圧力降下から漏洩量を求めた。
Leakage (airtightness);
A gasket test piece punched into a size of φ48mm × φ67mm is mounted between steel flanges of φ100mm × height 50mm and surface roughness Rmax = 12μm, and the surface pressure is 19.6MPa (200kgf / cm 2 G) by a compression tester. A load was applied. After applying a nitrogen gas internal pressure of 0.98 MPa (1.0 kgf / cm 2 G) to the inner diameter of the gasket from the pressure introduction through hole provided in the flange, the pressure introduction pipe was sealed and held for 1 hour. The pressure change before and after holding was read with a pressure sensor, and the amount of leakage was determined from the pressure drop.
引張り強さ;
JIS R3453に準拠して試験片を作成し引張り強さを測定した。
[実施例1]
PTFEファインパウダー(CD−1、旭硝子(株)製)400g、
NK−300(微粉末クレー、昭和KDE(株)製)600g、および
アイソパーC(炭化水素系有機溶剤、分留温度:97〜104℃、エクソンモービル(有))250g
をニーダーで5分間混合した後、室温(25℃)で16時間放置することにより熟成させ、シート形成用組成物を調製した。
Tensile strength;
Test pieces were prepared in accordance with JIS R3453 and the tensile strength was measured.
[Example 1]
400 g PTFE fine powder (CD-1, manufactured by Asahi Glass Co., Ltd.)
NK-300 (fine powder clay, manufactured by Showa KDE Co., Ltd.) 600 g, and Isopar C (hydrocarbon organic solvent, fractional distillation temperature: 97 to 104 ° C., Exxon Mobil (existing)) 250 g
After mixing with a kneader for 5 minutes, the mixture was aged by standing at room temperature (25 ° C.) for 16 hours to prepare a sheet-forming composition.
この組成物を、室温(25℃)で、口金300mm×20mmの押出機で押出し、プリフォームを作成した。
このプリフォームを、ロール径700mm、ロール間隔20mm、ロール速度6m/分、ロール温度40℃の条件下で二軸ロールにより圧延した。この圧延の直後に、得られたシートを、ロール間隔を10mmとして再度圧延した。さらに、この圧延の直後に、得ら
れたシートを、ロール間隔を5mmとして再度圧延した。最後に、この圧延の直後に、得られたシートを、ロール間隔を1.5mmとして再度圧延し、厚さ1.5mmのシートが得られた。
This composition was extruded at room temperature (25 ° C.) with a 300 mm × 20 mm die extruder to prepare a preform.
This preform was rolled by a biaxial roll under the conditions of a roll diameter of 700 mm, a roll interval of 20 mm, a roll speed of 6 m / min, and a roll temperature of 40 ° C. Immediately after this rolling, the obtained sheet was rolled again with a roll interval of 10 mm. Furthermore, immediately after this rolling, the obtained sheet was rolled again with a roll interval of 5 mm. Finally, immediately after this rolling, the obtained sheet was rolled again with a roll interval of 1.5 mm, and a sheet having a thickness of 1.5 mm was obtained.
このシートを室温(25℃)で24時間放置し溶剤を除去した後、電気炉内で350℃で3時間焼成し、シートガスケットを得た。
このシートガスケットの漏洩量(気密性)は4.0×10-5Pa・m3/s、引張り強さは11MPaであった。
The sheet was left at room temperature (25 ° C.) for 24 hours to remove the solvent, and then baked in an electric furnace at 350 ° C. for 3 hours to obtain a sheet gasket.
This sheet gasket had a leakage amount (air tightness) of 4.0 × 10 −5 Pa · m 3 / s and a tensile strength of 11 MPa.
[実施例2]
アイソパーC 250gに替えて、アイソパーC 125gおよびアイソパーG(炭化水素系有機溶剤、分留温度:158〜175℃、エクソンモービル(有))125gを用いた以外は実施例1と同様の方法でシートガスケットを製造した。
[Example 2]
The sheet was prepared in the same manner as in Example 1, except that 125 g of Isopar C and 125 g of Isopar G (hydrocarbon organic solvent, fractional distillation temperature: 158 to 175 ° C., Exxon Mobil) were used instead of 250 g of Isopar C. A gasket was manufactured.
このシートガスケットの漏洩量(気密性)は6.0×10-5Pa・m3/s、引張り強さは10MPaであった。
[実施例3]
ロール温度を40℃から80℃に変更した以外は実施例2と同様の方法でシートガスケットを製造した。
This sheet gasket had a leakage amount (airtightness) of 6.0 × 10 −5 Pa · m 3 / s and a tensile strength of 10 MPa.
[Example 3]
A sheet gasket was produced in the same manner as in Example 2 except that the roll temperature was changed from 40 ° C to 80 ° C.
このシートガスケットの漏洩量(気密性)は4.0×10-5Pa・m3/s、引張り強さは11MPaであった。
[比較例1]
アイソパーC 250gに替えてアイソパーG 250gを用い、ロール温度を40℃から80℃に変更した以外は実施例1と同様の方法でシートガスケットを製造した。
This sheet gasket had a leakage amount (air tightness) of 4.0 × 10 −5 Pa · m 3 / s and a tensile strength of 11 MPa.
[Comparative Example 1]
A sheet gasket was produced in the same manner as in Example 1 except that 250 g of Isopar C was used instead of 250 g of Isopar C and the roll temperature was changed from 40 ° C. to 80 ° C.
このシートガスケットの漏洩量(気密性)は1.0×10-4Pa・m3/s、引張り強さは11MPaであった。
[比較例2]
アイソパーC 250gに替えてアイソパーG 250gを用いた以外は実施例1と同様の方法でシートガスケットを製造した。
This sheet gasket had a leakage amount (air tightness) of 1.0 × 10 −4 Pa · m 3 / s and a tensile strength of 11 MPa.
[Comparative Example 2]
A sheet gasket was produced in the same manner as in Example 1 except that 250 g of Isopar G was used instead of 250 g of Isopar C.
このシートガスケットの漏洩量(気密性)は2.0×10-4Pa・m3/s、引張り強さは10MPaであった。
[比較例3]
アイソパーC 250gに替えてアイソパーM(炭化水素系有機溶剤、分留温度:21
8〜253℃、エクソンモービル(有))250gを用い、ロール温度を40℃から80℃に変更した以外は実施例1と同様の方法でシートガスケットを製造した。
This sheet gasket had a leakage amount (air tightness) of 2.0 × 10 −4 Pa · m 3 / s and a tensile strength of 10 MPa.
[Comparative Example 3]
Isopar C (hydrocarbon organic solvent, fractional distillation temperature: 21 instead of 250 g of Isopar C)
A sheet gasket was produced in the same manner as in Example 1 except that 250 g of 8 to 253 ° C. and Exxon Mobil (existing) was used and the roll temperature was changed from 40 ° C. to 80 ° C.
このシートガスケットの漏洩量(気密性)は8.0×10-4Pa・m3/s、引張り強さは10MPaであった。
[比較例4]
ロール温度を40℃から25℃に変更した以外は実施例1と同様の方法でシートガスケットを製造した。
This sheet gasket had a leakage amount (air tightness) of 8.0 × 10 −4 Pa · m 3 / s and a tensile strength of 10 MPa.
[Comparative Example 4]
A sheet gasket was produced in the same manner as in Example 1 except that the roll temperature was changed from 40 ° C to 25 ° C.
このシートガスケットの漏洩量(気密性)は4.0×10-4Pa・m3/s、引張り強さは10MPaであった。
[比較例5]
ロール温度を40℃から100℃に変更した以外は実施例1と同様の方法でシートガスケットを製造した。
This sheet gasket had a leakage amount (air tightness) of 4.0 × 10 −4 Pa · m 3 / s and a tensile strength of 10 MPa.
[Comparative Example 5]
A sheet gasket was produced in the same manner as in Example 1 except that the roll temperature was changed from 40 ° C to 100 ° C.
このシートガスケットの漏洩量(気密性)は1.0×10-3Pa・m3/s、引張り強さは6MPaで
あった。
This sheet gasket had a leakage amount (air tightness) of 1.0 × 10 −3 Pa · m 3 / s and a tensile strength of 6 MPa.
Claims (3)
該加工助剤が、分留温度が120℃以下である石油系炭化水素溶剤を30質量%以上(ただし、加工助剤重量を100質量%とする。)含む
充填材入りフッ素樹脂シートの製造方法によって製造され、
下記の特性(a)および(b)を充足する
ことを特徴とするガスケット用充填材入りフッ素樹脂シート;
特性(a):JIS R3453に準拠した引張り強さが8〜11MPaである、
特性(b):該充填材入りフッ素樹脂シートから作成したφ48mm×φ67mm×厚さ1.5mmの試験片に対して面圧19.6MPa、窒素ガス内圧0.98MPaとして気密試験を行った場合の漏洩量が4.0×10 -5 〜9×10-5Pa・m3/sである。 Including a step of rolling a sheet-forming resin composition containing a fluororesin, a filler and a processing aid at a roll temperature of 40 to 80 ° C.,
The processing aid contains 30% by mass or more of a petroleum hydrocarbon solvent having a fractional distillation temperature of 120 ° C. or less (provided that the weight of the processing aid is 100% by mass).
Manufactured by a method for producing a filled fluororesin sheet,
A fluororesin sheet with a filler for gaskets , characterized by satisfying the following characteristics (a) and (b);
Characteristic (a): Tensile strength based on JIS R3453 is 8 to 11 MPa,
Characteristic (b): The amount of leakage when an airtight test is performed on a test piece of φ48 mm × φ67 mm × thickness 1.5 mm made from the filled fluororesin sheet with a surface pressure of 19.6 MPa and nitrogen gas internal pressure of 0.98 MPa. It is 4.0 × 10 −5 to 9 × 10 −5 Pa · m 3 / s.
Priority Applications (1)
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JP2008152764A JP4777389B2 (en) | 2008-06-11 | 2008-06-11 | Fluororesin sheet with gasket filler and gasket |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2008152764A JP4777389B2 (en) | 2008-06-11 | 2008-06-11 | Fluororesin sheet with gasket filler and gasket |
Related Parent Applications (1)
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JP2006082674A Division JP4213167B2 (en) | 2006-03-24 | 2006-03-24 | Method for producing filled fluororesin sheet |
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