WO2010050366A1 - Tube - Google Patents
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- Publication number
- WO2010050366A1 WO2010050366A1 PCT/JP2009/067872 JP2009067872W WO2010050366A1 WO 2010050366 A1 WO2010050366 A1 WO 2010050366A1 JP 2009067872 W JP2009067872 W JP 2009067872W WO 2010050366 A1 WO2010050366 A1 WO 2010050366A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- inner layer
- fluororesin
- layer
- tubular body
- silicone rubber
- Prior art date
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- 229920002379 silicone rubber Polymers 0.000 claims abstract description 28
- 239000004945 silicone rubber Substances 0.000 claims abstract description 28
- 239000000853 adhesive Substances 0.000 claims abstract description 15
- 230000001070 adhesive effect Effects 0.000 claims abstract description 15
- 125000000524 functional group Chemical group 0.000 claims abstract description 13
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 8
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 4
- 125000004018 acid anhydride group Chemical group 0.000 claims description 3
- 239000010410 layer Substances 0.000 abstract description 97
- 239000000126 substance Substances 0.000 abstract description 16
- 239000011229 interlayer Substances 0.000 abstract 3
- 230000032798 delamination Effects 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 description 13
- 230000000052 comparative effect Effects 0.000 description 8
- 238000001125 extrusion Methods 0.000 description 7
- 239000000178 monomer Substances 0.000 description 7
- 238000004073 vulcanization Methods 0.000 description 7
- 238000012644 addition polymerization Methods 0.000 description 5
- 239000002356 single layer Substances 0.000 description 5
- 238000004381 surface treatment Methods 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000005060 rubber Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 230000002093 peripheral effect Effects 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 239000002033 PVDF binder Substances 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 229920002313 fluoropolymer Polymers 0.000 description 2
- 239000004811 fluoropolymer Substances 0.000 description 2
- 238000013007 heat curing Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- 238000009832 plasma treatment Methods 0.000 description 2
- -1 polytetrafluoroethylene Polymers 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000012756 surface treatment agent Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
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
- F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
- F16L9/00—Rigid pipes
- F16L9/12—Rigid pipes of plastics with or without reinforcement
- F16L9/121—Rigid pipes of plastics with or without reinforcement with three layers
-
- 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
- B32B1/00—Layered products having a non-planar shape
- B32B1/08—Tubular products
-
- 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
- B32B25/00—Layered products comprising a layer of natural or synthetic rubber
- B32B25/04—Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B25/08—Layered products comprising a layer of natural or synthetic rubber comprising rubber as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- 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
- B32B25/00—Layered products comprising a layer of natural or synthetic rubber
- B32B25/20—Layered products comprising a layer of natural or synthetic rubber comprising silicone rubber
-
- 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
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- 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
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
- B32B27/322—Layered products comprising a layer of synthetic resin comprising polyolefins comprising halogenated polyolefins, e.g. PTFE
-
- 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
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- 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
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/714—Inert, i.e. inert to chemical degradation, corrosion
-
- 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
- B32B2457/00—Electrical equipment
-
- 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
- B32B2535/00—Medical equipment, e.g. bandage, prostheses or catheter
Definitions
- the present invention relates to a tubular body having a laminated structure, for example, a tubular body used for piping of pharmaceutical manufacturing equipment, semiconductor manufacturing equipment, food manufacturing equipment and the like.
- Tubular bodies used in pipes for pharmaceutical manufacturing facilities have chemical stability such as chemical resistance, heat resistance, and dissolution, and physical durability such as flexibility (flexibility and flexibility) and pressure resistance. Is required.
- Japanese Patent Application Laid-Open No. 2001-12659 discloses a two-layered tubular body having an inner layer made of fluororesin and an outer layer made of addition-polymerized silicone rubber. According to this tubular body, chemical stability such as chemical resistance, heat resistance, and dissolution property is ensured by the fluororesin, and physical durability such as flexibility and pressure resistance is ensured by the addition polymerization type silicone rubber. .
- this tubular body is provided with a primer treatment portion treated with a chemical treatment and a silicone rubber primer outside the inner layer made of fluororesin, and an inner layer made of fluororesin and an outer layer made of addition polymerization silicone rubber, Are integrated by cross-linking adhesion.
- the peel strength between the inner layer made of fluororesin and the outer layer made of addition-polymerized silicone rubber can be increased, and the two-layered tubular body can be used over a long period of time.
- the outer surface of the fluororesin inner layer needs to be subjected to a surface treatment with a chemical treatment and a silicone rubber primer, which makes the manufacturing process complicated and increases the number of steps. For this reason, the tubular body of a two-layer structure may become expensive.
- a two-layer tubular body is used for sliding applications such as a tube pump, a large sliding resistance is applied between the fluororesin inner layer and the addition polymerization silicone rubber outer layer. The sliding resistance may be larger than the peel strength obtained by the primer treatment. For this reason, there is a possibility that the inner layer made of the fluororesin and the outer layer made of the addition polymerization type silicone rubber are peeled off.
- the present invention has been made under the circumstances described above, and the object of the present invention is a low-cost laminated structure that is excellent in chemical stability, physical durability, flexibility, and adhesion between laminates.
- the object is to provide a tubular body.
- the laminated structure tubular body of the present invention comprises an inner layer made of a thermoplastic fluororesin, an intermediate layer made of a fluororesin having an adhesive functional group coated on the outer periphery of the inner layer, and the intermediate layer. And an outer layer made of silicone rubber coated on the outer periphery of the layer. According to this tubular body, chemical stability is ensured because the inner layer is formed of a fluororesin, and physical durability is ensured because the outer layer is formed of silicone rubber.
- an intermediate layer made of a fluororesin having an adhesive functional group is interposed between the inner layer and the outer layer without performing a primer treatment on the outer side of the inner layer after a physical treatment such as a conventional chemical treatment or plasma treatment.
- a physical treatment such as a conventional chemical treatment or plasma treatment.
- the fluororesin having an adhesive functional group is a tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (modified PFA) having a hydroxyl group or an acid anhydride group. Since the intermediate layer is formed of such a material having a specific adhesive functional group, a large adhesive strength can be obtained, and it can be easily manufactured without requiring a complicated manufacturing process so far. Increase in body costs can be suppressed. Examples of polymers constituting the modified PFA having the hydroxyl group described above will be described below.
- thermoplastic fluoropolymer containing a hydroxyl group can be obtained by copolymerization of a monomer (monomer) containing a hydroxyl group and a monomer (monomer) containing no hydroxyl group.
- a monomer (monomer) containing a hydroxyl group a monomer (monomer) containing no hydroxyl group.
- the monomer containing a hydroxyl group is shown below, the monomer containing a hydroxyl group is not restrict
- X is H (hydrogen) or F (
- FIGS. 1A and 1B are a perspective view and a cross-sectional view taken along line AA showing a laminated structure of tubular bodies according to an embodiment of the present invention.
- FIG. 2 is a graph showing the results of peel strength and the like of each tubular body of Example 1 and Comparative Examples 1 and 2.
- Absent. 1 (A) and 1 (B) are a perspective view and a cross-sectional view taken along line AA showing a laminated structure of an embodiment of a tubular body of the present invention.
- the tubular body 1 is a laminated tube or hose, and has a triple structure having an inner layer 11, an intermediate layer 12 coated on the outer periphery of the inner layer 11, and an outer layer 13 coated on the outer periphery of the intermediate layer 12. Is formed.
- the inner layer 11 is formed of a thermoplastic fluororesin excellent in chemical stability such as chemical resistance, heat resistance, and elution
- the intermediate layer 12 is formed of a fluororesin having an adhesive functional group.
- the thermoplastic fluororesin of the inner layer 11 include tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (PFA), ethylene-tetrafluoroethylene copolymer (ETFE), tetrafluoroethylene-hexafluoropropylene copolymer ( FEP), polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF) and the like are used alone or in combination.
- PFA which is excellent in chemical resistance and stress crack resistance and easy to process by melt extrusion is preferable.
- fluororesin having an adhesive functional group of the intermediate layer 12 PFA (modified PFA) having a hydroxyl group or an acid anhydride group is used.
- silicone rubber of the outer layer 13 heat curable millable rubber, heat curable liquid rubber, or the like is used.
- crosslinking mechanism of these rubbers there are organic peroxide crosslinking and addition reaction crosslinking.
- a heat-curing type millable rubber excellent in flexibility is cross-linked with an organic peroxide.
- the tubular body 1 having such a configuration is formed by the following procedure.
- a two-layered molded article having a thermoplastic fluororesin as an inner layer 11 and a fluororesin having an adhesive functional group as an intermediate layer 12 is formed by coextrusion with a biaxial extruder.
- a three-layered molded body having a silicone rubber outer layer 13 formed on the outer periphery of the two-layered molded body, that is, the outer periphery of the intermediate layer 12 is formed by extrusion using a single screw extruder.
- the outer layer 13 is solidified by heat vulcanizing the molded article having a three-layer structure in a thermostatic bath.
- the tubular body 1 is completed by the above procedure.
- Each process of co-extrusion molding of a two-layer structure molded body, extrusion molding of a three-layer structure molded body, and thermal vulcanization of a three-layer structure molded body can be performed by batch processing or continuous processing.
- the tubular body 1 configured as described above chemical stability is ensured because the inner layer 11 is formed of a fluororesin, and physical durability and flexibility are formed of the outer layer 13 of silicone rubber. Will be secured.
- the intermediate layer 12 made of a fluororesin having an adhesive functional group between the inner layer 11 and the outer layer 13 is formed together with the inner layer 11 without subjecting the outer surface of the inner layer 11 to surface treatment such as conventional primer treatment or plasma treatment.
- the peel strength between the inner layer 11 and the outer layer 13 can be increased. Therefore, the manufacturing process can be simplified and the number of man-hours can be reduced. Furthermore, since the intermediate layer 12 is formed of a material having a specific adhesive functional group called modified PFA, a large adhesive strength can be obtained, It can manufacture easily without requiring the complicated manufacturing process until now, and can suppress the cost increase of the tubular body 1. Furthermore, it has been confirmed by experiments conducted by the inventors described later that the peel strength obtained by the intermediate layer 12 is greater than the peel strength obtained by the conventional surface treatment.
- each tubular body of Example 1 and Comparative Examples 1 and 2 was produced as follows, and the peel strength and the like were examined.
- PFA manufactured by Daikin Industries, P62XP
- modified PFA manufactured by Daikin Industries, RAP1RC
- RAP1RC modified PFA
- heat-curing type millable silicone rubber manufactured by Shin-Etsu Chemical Co., KE551-U
- a vulcanizing agent manufactured by Shin-Etsu Chemical Co., Ltd., C-273 are selected for the outer layer, and both are kneaded at a mass ratio of 100: 1.
- a three-layered molded body having an outer diameter of 6.8 mm was produced by extrusion molding together with a two-layered molded body. Then, the molded body having a three-layer structure is heated at a primary vulcanization temperature of 140 ° C. for 1 hour, and further heated at a secondary vulcanization temperature of 200 ° C.
- thermosetting millable silicone rubber A tubular body having a three-layer structure was produced.
- PFA manufactured by Daikin Industries, P62XP
- PFA was extruded to form a single-layer molded body having an inner diameter of 4.1 mm and an outer diameter of 4.4 mm.
- the surface of only the outer peripheral surface of the single-layer molded body is treated using a fluoropolymer surface treatment agent (manufactured by Junko Co., Ltd., Tetraetch (registered trademark), a liquid obtained by dissolving sodium / naphthalene complex in a solvent)
- a fluoropolymer surface treatment agent manufactured by Junko Co., Ltd., Tetraetch (registered trademark)
- Tetraetch registered trademark
- a heat curable millable silicone rubber manufactured by Shin-Etsu Chemical Co., KE551-U
- a vulcanizing agent manufactured by Shin-Etsu Chemical Co., Ltd., C-273
- both are kneaded at a mass ratio of 100: 1 to be a primer treatment.
- a two-layered molded product having an outer diameter of 6.8 mm was produced by extrusion molding together with the molded product having the single-layered structure. Then, the two-layered molded body is heated at a primary vulcanization temperature of 140 ° C. for 1 hour, and further heated at a secondary vulcanization temperature of 200 ° C.
- thermosetting millable silicone rubber A two-layered tubular body was produced.
- PFA manufactured by Daikin Industries, P62XP
- P62XP was extruded to form a single-layer molded body having an inner diameter of 4.1 mm and an outer diameter of 4.4 mm.
- the outer peripheral surface of the molded article having a single layer structure was subjected to a primer treatment using a silicone rubber primer.
- a heat curable millable silicone rubber manufactured by Shin-Etsu Chemical Co., KE551-U
- a vulcanizing agent manufactured by Shin-Etsu Chemical Co., Ltd., C-273
- both are kneaded at a mass ratio of 100: 1 to be a primer treatment.
- a two-layered molded product having an outer diameter of 6.8 mm was produced by extrusion molding together with the molded product having the single-layered structure. Then, the two-layered molded body is heated at a primary vulcanization temperature of 140 ° C. for 1 hour, and further heated at a secondary vulcanization temperature of 200 ° C.
- FIG. 2 is a diagram showing the results of peel strength, standard deviation, and fracture cross section of each tubular body of Example 1 and Comparative Example 1.2.
- the fracture cross section is an interface in both Example 1 and Comparative Examples 1 and 2, and thus the peel strength was measured.
- Example 1 an intermediate layer of modified PFA was used between the inner layer and the outer layer, but the peel strength was as high as 11.6 N.
- Comparative Example 1 is a case where the inner layer is subjected to chemical surface treatment and primer treatment, but the peel strength is 6.76 N, which is significantly lower than that of Example 1, and Comparative Example 2 is a primer on the inner layer.
- the peel strength was 0.00 N, and the inner layer and the outer layer were not adhered at all and were not suitable for practical use. From this, it can be said that it is preferable that the intermediate layer made of modified PFA is interposed between the inner layer made of thermoplastic fluororesin and the outer layer made of silicone rubber because of excellent adhesiveness between the layers. .
- the tubular body according to the present invention is particularly effective as piping for pharmaceutical manufacturing equipment, semiconductor manufacturing equipment, food manufacturing equipment, etc., but can also be applied, for example, as piping built in electronic equipment or the like.
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- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Laminated Bodies (AREA)
- Rigid Pipes And Flexible Pipes (AREA)
Abstract
A tube (1) of a multilayer structure which comprises: an inner layer (11) constituted of a thermoplastic fluororesin; an interlayer (12) which is constituted of a fluororesin having an adhesive functional group and with which the outer periphery of the inner layer has been coated; and an outer layer (13) which is constituted of a silicone rubber and with which the outer periphery of the interlayer has been coated. As a result, the fluororesin constituting the inner layer ensures chemical stability, and the silicone rubber constituting the outer layer ensures physical durability and flexibility. The interposition of the interlayer constituted of a fluororesin having an adhesive functional group between the inner layer and the outer layer brings about excellent adhesion between the superposed layers and can enhance peel strength between the inner layer and outer layer. Thus, the tube is produced through a smaller number of simplified steps and can hence be inhibited from increasing in cost. Even when used in a sliding application, the tube can be prevented from suffering the delamination caused by sliding resistance imposed between the inner layer and the outer layer.
Description
本発明は、積層構造の管状体に関し、例えば医薬品製造設備、半導体製造設備、食品製造設備等の配管に用いられる管状体に関する。
The present invention relates to a tubular body having a laminated structure, for example, a tubular body used for piping of pharmaceutical manufacturing equipment, semiconductor manufacturing equipment, food manufacturing equipment and the like.
医薬品製造設備等の配管に用いられる管状体は、耐薬品性、耐熱性、溶出性等の化学的安定性や柔軟性(可撓性、屈曲性)、耐圧性等の物理的耐久性を有することが求められる。これらを満足する管状体として、特開2001−12659号公報にはフッ素樹脂製の内側層と付加重合系シリコーンゴム製の外側層とを有する2層構造の管状体が開示されている。この管状体によれば、フッ素樹脂により耐薬品性、耐熱性、溶出性等の化学的安定性が担保され、付加重合系シリコーンゴムにより柔軟性、耐圧性等の物理的耐久性が担保される。しかし、一般的に、フッ素樹脂とシリコーンゴムとの接着性は低いため、2層構造の管状体の使用が長期にわたるとフッ素樹脂製の内側層と付加重合系シリコーンゴム製の外側層との間が剥離するおそれがある。
そこで、この管状体は、フッ素樹脂製の内側層の外側に化学処理及びシリコーンゴム系プライマで処理したプライマ処理部を設けて、フッ素樹脂製の内側層と付加重合系シリコーンゴム製の外側層とを架橋接着により一体化している。これにより、フッ素樹脂製の内側層と付加重合系シリコーンゴム製の外側層との間のピール強度を高めることができ、2層構造の管状体を長期間にわたって使用することが可能なようにしている。
上述した2層構造の管状体では、フッ素樹脂製の内側層の外側を化学処理及びシリコーンゴム系プライマで表面処理する必要があるため、製造工程が煩雑となって工数が増加する。このため、2層構造の管状体がコスト高となる場合がある。また、2層構造の管状体を例えばチューブポンプ等の摺動用途に使用する場合は、フッ素樹脂製の内側層と付加重合系シリコーンゴム製の外側層との間に大きな摺動抵抗が掛かるが、この摺動抵抗はプライマ処理により得られるピール強度よりも大きくなる場合がある。このため、フッ素樹脂製の内側層と付加重合系シリコーンゴム製の外側層との間が剥離するおそれがある。 Tubular bodies used in pipes for pharmaceutical manufacturing facilities have chemical stability such as chemical resistance, heat resistance, and dissolution, and physical durability such as flexibility (flexibility and flexibility) and pressure resistance. Is required. As a tubular body that satisfies these requirements, Japanese Patent Application Laid-Open No. 2001-12659 discloses a two-layered tubular body having an inner layer made of fluororesin and an outer layer made of addition-polymerized silicone rubber. According to this tubular body, chemical stability such as chemical resistance, heat resistance, and dissolution property is ensured by the fluororesin, and physical durability such as flexibility and pressure resistance is ensured by the addition polymerization type silicone rubber. . However, in general, the adhesiveness between the fluororesin and the silicone rubber is low, and therefore, when the tubular body having a two-layer structure is used for a long period of time, there is a gap between the fluororesin inner layer and the addition polymerization silicone rubber outer layer. May peel off.
Therefore, this tubular body is provided with a primer treatment portion treated with a chemical treatment and a silicone rubber primer outside the inner layer made of fluororesin, and an inner layer made of fluororesin and an outer layer made of addition polymerization silicone rubber, Are integrated by cross-linking adhesion. As a result, the peel strength between the inner layer made of fluororesin and the outer layer made of addition-polymerized silicone rubber can be increased, and the two-layered tubular body can be used over a long period of time. Yes.
In the above-described two-layered tubular body, the outer surface of the fluororesin inner layer needs to be subjected to a surface treatment with a chemical treatment and a silicone rubber primer, which makes the manufacturing process complicated and increases the number of steps. For this reason, the tubular body of a two-layer structure may become expensive. When a two-layer tubular body is used for sliding applications such as a tube pump, a large sliding resistance is applied between the fluororesin inner layer and the addition polymerization silicone rubber outer layer. The sliding resistance may be larger than the peel strength obtained by the primer treatment. For this reason, there is a possibility that the inner layer made of the fluororesin and the outer layer made of the addition polymerization type silicone rubber are peeled off.
そこで、この管状体は、フッ素樹脂製の内側層の外側に化学処理及びシリコーンゴム系プライマで処理したプライマ処理部を設けて、フッ素樹脂製の内側層と付加重合系シリコーンゴム製の外側層とを架橋接着により一体化している。これにより、フッ素樹脂製の内側層と付加重合系シリコーンゴム製の外側層との間のピール強度を高めることができ、2層構造の管状体を長期間にわたって使用することが可能なようにしている。
上述した2層構造の管状体では、フッ素樹脂製の内側層の外側を化学処理及びシリコーンゴム系プライマで表面処理する必要があるため、製造工程が煩雑となって工数が増加する。このため、2層構造の管状体がコスト高となる場合がある。また、2層構造の管状体を例えばチューブポンプ等の摺動用途に使用する場合は、フッ素樹脂製の内側層と付加重合系シリコーンゴム製の外側層との間に大きな摺動抵抗が掛かるが、この摺動抵抗はプライマ処理により得られるピール強度よりも大きくなる場合がある。このため、フッ素樹脂製の内側層と付加重合系シリコーンゴム製の外側層との間が剥離するおそれがある。 Tubular bodies used in pipes for pharmaceutical manufacturing facilities have chemical stability such as chemical resistance, heat resistance, and dissolution, and physical durability such as flexibility (flexibility and flexibility) and pressure resistance. Is required. As a tubular body that satisfies these requirements, Japanese Patent Application Laid-Open No. 2001-12659 discloses a two-layered tubular body having an inner layer made of fluororesin and an outer layer made of addition-polymerized silicone rubber. According to this tubular body, chemical stability such as chemical resistance, heat resistance, and dissolution property is ensured by the fluororesin, and physical durability such as flexibility and pressure resistance is ensured by the addition polymerization type silicone rubber. . However, in general, the adhesiveness between the fluororesin and the silicone rubber is low, and therefore, when the tubular body having a two-layer structure is used for a long period of time, there is a gap between the fluororesin inner layer and the addition polymerization silicone rubber outer layer. May peel off.
Therefore, this tubular body is provided with a primer treatment portion treated with a chemical treatment and a silicone rubber primer outside the inner layer made of fluororesin, and an inner layer made of fluororesin and an outer layer made of addition polymerization silicone rubber, Are integrated by cross-linking adhesion. As a result, the peel strength between the inner layer made of fluororesin and the outer layer made of addition-polymerized silicone rubber can be increased, and the two-layered tubular body can be used over a long period of time. Yes.
In the above-described two-layered tubular body, the outer surface of the fluororesin inner layer needs to be subjected to a surface treatment with a chemical treatment and a silicone rubber primer, which makes the manufacturing process complicated and increases the number of steps. For this reason, the tubular body of a two-layer structure may become expensive. When a two-layer tubular body is used for sliding applications such as a tube pump, a large sliding resistance is applied between the fluororesin inner layer and the addition polymerization silicone rubber outer layer. The sliding resistance may be larger than the peel strength obtained by the primer treatment. For this reason, there is a possibility that the inner layer made of the fluororesin and the outer layer made of the addition polymerization type silicone rubber are peeled off.
本発明は、上述した事情からなされたものであり、本発明の目的は、化学的安定性及び物理的耐久性、柔軟性に優れ、さらに積層間の接着性に優れた低コストの積層構造の管状体を提供することにある。
上記目的達成のため、本発明の積層構造の管状体は、熱可塑性のフッ素樹脂で成る内層と、該内層の外周に被覆された接着性官能基を有するフッ素樹脂で成る中間層と、該中間層の外周に被覆されたシリコーン系のゴムで成る外層とを有することを特徴としている。この管状体によれば、内層がフッ素樹脂により形成されているため化学的安定性が担保され、外層がシリコーン系のゴムにより形成されているため物理的耐久性が担保される。そして、従来の化学処理もしくはプラズマ処理のような物理処理の後にプライマ処理を内層の外側に施さなくても、内層と外層との間に接着性官能基を有するフッ素樹脂で成る中間層を介在させることにより内層と外層とのピール強度を高めることができるので、製造工程が簡易となって工数を低減させ管状体のコスト増を抑えることができる。さらに、中間層が介在することにより得られる上記ピール強度は、従来の表面処理により得られるピール強度よりも大きくなることが後述する実験により明らかとなったので、本発明の管状体を摺動用途に使用しても内層と外層との間に掛かる摺動抵抗による剥離を防止することができ、かかる管状体を長期間にわたって使用することができる。
前記接着性官能基を有するフッ素樹脂は、ヒドロキシル基あるいは酸無水物基を有するテトラフルオロエチレン−パーフルオロアルキルビニルエーテル共重合体(変性PFA)であることを特徴としている。このような特定の接着性官能基を有する材料により中間層を形成しているので、大きな接着強度が得られると共に、これまでの煩雑な製造工程を必要とすることなく、容易に製造でき、管状体のコスト増を抑えることができる。なお、上記したヒドロキシル基を有する変性PFAを構成するポリマの例について以下に述べる。
ヒドロキシル基を含む熱可塑性フッ素ポリマは、ヒドロキシル基を含む単量体(モノマ)とヒドロキシル基を含まない単量体(モノマ)との共重合で得ることができる。ヒドロキシル基を含む単量体の例を以下に示すが、ヒドロキシル基を含む単量体はこれらに制限されることはなく、適用可能なその他のヒドロキシル基を含む単量体であっても良い。
CF2=CF−R−CH2−OH,
CH3=CH−R−CH2−OH,
CF2=CH−R−CH2−OH,
CF2=CF−O−R−CH2−OH,
CH2=CH−O−R−CH2−OH,
CF2=CFCF2−O−R−CH2−OH,
CH2=CFCF2−R−CH2−OH,
CH2=CFCF2−O−R−CH2−OH,
なお、Rは、
a:−(CX2)l−,
b:−(OCF(CF3)CF2)m−,
c:−(OCF2CF(CF3))m−,
d:−(OCF(CF3))n−,
e:−(OCF2CF2)n−,
の中から選択された何れか1つ又は2つ以上の組み合わせである。
また、XはH(水素)又はF(フッ素)であり、
l:0~40、m:0~10、n:0~10である。 The present invention has been made under the circumstances described above, and the object of the present invention is a low-cost laminated structure that is excellent in chemical stability, physical durability, flexibility, and adhesion between laminates. The object is to provide a tubular body.
In order to achieve the above object, the laminated structure tubular body of the present invention comprises an inner layer made of a thermoplastic fluororesin, an intermediate layer made of a fluororesin having an adhesive functional group coated on the outer periphery of the inner layer, and the intermediate layer. And an outer layer made of silicone rubber coated on the outer periphery of the layer. According to this tubular body, chemical stability is ensured because the inner layer is formed of a fluororesin, and physical durability is ensured because the outer layer is formed of silicone rubber. Then, an intermediate layer made of a fluororesin having an adhesive functional group is interposed between the inner layer and the outer layer without performing a primer treatment on the outer side of the inner layer after a physical treatment such as a conventional chemical treatment or plasma treatment. As a result, the peel strength between the inner layer and the outer layer can be increased, which simplifies the manufacturing process, reduces the number of steps, and suppresses the cost increase of the tubular body. Furthermore, since it became clear by experiments described later that the peel strength obtained by the intermediate layer is greater than the peel strength obtained by the conventional surface treatment, the tubular body of the present invention is used for sliding. Even if used, it is possible to prevent peeling due to sliding resistance between the inner layer and the outer layer, and such a tubular body can be used for a long period of time.
The fluororesin having an adhesive functional group is a tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (modified PFA) having a hydroxyl group or an acid anhydride group. Since the intermediate layer is formed of such a material having a specific adhesive functional group, a large adhesive strength can be obtained, and it can be easily manufactured without requiring a complicated manufacturing process so far. Increase in body costs can be suppressed. Examples of polymers constituting the modified PFA having the hydroxyl group described above will be described below.
The thermoplastic fluoropolymer containing a hydroxyl group can be obtained by copolymerization of a monomer (monomer) containing a hydroxyl group and a monomer (monomer) containing no hydroxyl group. Although the example of the monomer containing a hydroxyl group is shown below, the monomer containing a hydroxyl group is not restrict | limited to these, The monomer containing another applicable hydroxyl group may be sufficient.
CF 2 = CF-R-CH 2 -OH,
CH 3 = CH-R-CH 2 -OH,
CF 2 = CH-R-CH 2 -OH,
CF 2 = CF-O-R -CH 2 -OH,
CH 2 = CH-O-R -CH 2 -OH,
CF 2 = CFCF 2 —O—R—CH 2 —OH,
CH 2 = CFCF 2 -R-CH 2 -OH,
CH 2 = CFCF 2 -O-R -CH 2 -OH,
R is
a:-(CX 2 ) l- ,
b :-( OCF (CF 3) CF 2) m -,
c :-( OCF 2 CF (CF 3 )) m -,
d :-( OCF (CF 3)) n -,
e :-( OCF 2 CF 2) n -,
Any one or a combination of two or more selected from the above.
X is H (hydrogen) or F (fluorine);
l: 0 to 40, m: 0 to 10, and n: 0 to 10.
上記目的達成のため、本発明の積層構造の管状体は、熱可塑性のフッ素樹脂で成る内層と、該内層の外周に被覆された接着性官能基を有するフッ素樹脂で成る中間層と、該中間層の外周に被覆されたシリコーン系のゴムで成る外層とを有することを特徴としている。この管状体によれば、内層がフッ素樹脂により形成されているため化学的安定性が担保され、外層がシリコーン系のゴムにより形成されているため物理的耐久性が担保される。そして、従来の化学処理もしくはプラズマ処理のような物理処理の後にプライマ処理を内層の外側に施さなくても、内層と外層との間に接着性官能基を有するフッ素樹脂で成る中間層を介在させることにより内層と外層とのピール強度を高めることができるので、製造工程が簡易となって工数を低減させ管状体のコスト増を抑えることができる。さらに、中間層が介在することにより得られる上記ピール強度は、従来の表面処理により得られるピール強度よりも大きくなることが後述する実験により明らかとなったので、本発明の管状体を摺動用途に使用しても内層と外層との間に掛かる摺動抵抗による剥離を防止することができ、かかる管状体を長期間にわたって使用することができる。
前記接着性官能基を有するフッ素樹脂は、ヒドロキシル基あるいは酸無水物基を有するテトラフルオロエチレン−パーフルオロアルキルビニルエーテル共重合体(変性PFA)であることを特徴としている。このような特定の接着性官能基を有する材料により中間層を形成しているので、大きな接着強度が得られると共に、これまでの煩雑な製造工程を必要とすることなく、容易に製造でき、管状体のコスト増を抑えることができる。なお、上記したヒドロキシル基を有する変性PFAを構成するポリマの例について以下に述べる。
ヒドロキシル基を含む熱可塑性フッ素ポリマは、ヒドロキシル基を含む単量体(モノマ)とヒドロキシル基を含まない単量体(モノマ)との共重合で得ることができる。ヒドロキシル基を含む単量体の例を以下に示すが、ヒドロキシル基を含む単量体はこれらに制限されることはなく、適用可能なその他のヒドロキシル基を含む単量体であっても良い。
CF2=CF−R−CH2−OH,
CH3=CH−R−CH2−OH,
CF2=CH−R−CH2−OH,
CF2=CF−O−R−CH2−OH,
CH2=CH−O−R−CH2−OH,
CF2=CFCF2−O−R−CH2−OH,
CH2=CFCF2−R−CH2−OH,
CH2=CFCF2−O−R−CH2−OH,
なお、Rは、
a:−(CX2)l−,
b:−(OCF(CF3)CF2)m−,
c:−(OCF2CF(CF3))m−,
d:−(OCF(CF3))n−,
e:−(OCF2CF2)n−,
の中から選択された何れか1つ又は2つ以上の組み合わせである。
また、XはH(水素)又はF(フッ素)であり、
l:0~40、m:0~10、n:0~10である。 The present invention has been made under the circumstances described above, and the object of the present invention is a low-cost laminated structure that is excellent in chemical stability, physical durability, flexibility, and adhesion between laminates. The object is to provide a tubular body.
In order to achieve the above object, the laminated structure tubular body of the present invention comprises an inner layer made of a thermoplastic fluororesin, an intermediate layer made of a fluororesin having an adhesive functional group coated on the outer periphery of the inner layer, and the intermediate layer. And an outer layer made of silicone rubber coated on the outer periphery of the layer. According to this tubular body, chemical stability is ensured because the inner layer is formed of a fluororesin, and physical durability is ensured because the outer layer is formed of silicone rubber. Then, an intermediate layer made of a fluororesin having an adhesive functional group is interposed between the inner layer and the outer layer without performing a primer treatment on the outer side of the inner layer after a physical treatment such as a conventional chemical treatment or plasma treatment. As a result, the peel strength between the inner layer and the outer layer can be increased, which simplifies the manufacturing process, reduces the number of steps, and suppresses the cost increase of the tubular body. Furthermore, since it became clear by experiments described later that the peel strength obtained by the intermediate layer is greater than the peel strength obtained by the conventional surface treatment, the tubular body of the present invention is used for sliding. Even if used, it is possible to prevent peeling due to sliding resistance between the inner layer and the outer layer, and such a tubular body can be used for a long period of time.
The fluororesin having an adhesive functional group is a tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (modified PFA) having a hydroxyl group or an acid anhydride group. Since the intermediate layer is formed of such a material having a specific adhesive functional group, a large adhesive strength can be obtained, and it can be easily manufactured without requiring a complicated manufacturing process so far. Increase in body costs can be suppressed. Examples of polymers constituting the modified PFA having the hydroxyl group described above will be described below.
The thermoplastic fluoropolymer containing a hydroxyl group can be obtained by copolymerization of a monomer (monomer) containing a hydroxyl group and a monomer (monomer) containing no hydroxyl group. Although the example of the monomer containing a hydroxyl group is shown below, the monomer containing a hydroxyl group is not restrict | limited to these, The monomer containing another applicable hydroxyl group may be sufficient.
CF 2 = CF-R-CH 2 -OH,
CH 3 = CH-R-CH 2 -OH,
CF 2 = CH-R-CH 2 -OH,
CF 2 = CF-O-R -CH 2 -OH,
CH 2 = CH-O-R -CH 2 -OH,
CF 2 = CFCF 2 —O—R—CH 2 —OH,
CH 2 = CFCF 2 -R-CH 2 -OH,
CH 2 = CFCF 2 -O-R -CH 2 -OH,
R is
a:-(CX 2 ) l- ,
b :-( OCF (CF 3) CF 2) m -,
c :-( OCF 2 CF (CF 3 )) m -,
d :-( OCF (CF 3)) n -,
e :-( OCF 2 CF 2) n -,
Any one or a combination of two or more selected from the above.
X is H (hydrogen) or F (fluorine);
l: 0 to 40, m: 0 to 10, and n: 0 to 10.
第1図(A)及び(B)は、本発明の実施形態に係る管状体の積層構造を示す斜視図及びA−A線断面図である。
第2図は、実施例1、比較例1,2の各管状体のピール強度等の結果を示す図である。 FIGS. 1A and 1B are a perspective view and a cross-sectional view taken along line AA showing a laminated structure of tubular bodies according to an embodiment of the present invention.
FIG. 2 is a graph showing the results of peel strength and the like of each tubular body of Example 1 and Comparative Examples 1 and 2.
第2図は、実施例1、比較例1,2の各管状体のピール強度等の結果を示す図である。 FIGS. 1A and 1B are a perspective view and a cross-sectional view taken along line AA showing a laminated structure of tubular bodies according to an embodiment of the present invention.
FIG. 2 is a graph showing the results of peel strength and the like of each tubular body of Example 1 and Comparative Examples 1 and 2.
以下、本発明の実施形態について説明する。尚、以下に説明する実施形態は特許請求の範囲に係る発明を限定するものではなく、また実施形態の中で説明されている特徴の組み合わせの全てが発明の解決手段に必須であるとは限らない。
第1図(A)、(B)は、本発明の管状体の実施形態の積層構造を示す斜視図及びA−A線断面図である。この管状体1は、積層のチューブもしくはホースであり、内層11と、該内層11の外周に被覆された中間層12と、該中間層12の外周に被覆された外層13とを有する3重構造に形成されている。内層11は、耐薬品性、耐熱性、溶出性等の化学的安定性に優れた熱可塑性のフッ素樹脂で形成され、中間層12は、接着性官能基を有するフッ素樹脂で形成され、外層13は、柔軟性、耐圧性等の物理的耐久性に優れたシリコーン系のゴムで形成されている。
内層11の熱可塑性のフッ素樹脂としては、テトラフルオロエチレン−パーフルオロアルキルビニルエーテル共重合体(PFA)、エチレン−テトラフルオロエチレン共重合体(ETFE)、テトラフルオロエチレン−ヘキサフルオロプロピレンコ共重合体(FEP)、ポリテトラフルオロエチレン(PTFE)、ポリフッ化ビニリデン(PVDF)等の中から単独もしくはこれらの組み合わせが選択して使用される。特に、耐薬品性や耐ストレスクラック性に優れ、溶融押出しによる加工が容易なPFAが好ましい。
中間層12の接着性官能基を有するフッ素樹脂としては、ヒドロキシル基あるいは酸無水物基を有するPFA(変性PFA)が使用される。
外層13のシリコーン系のゴムとしては、加熱硬化型ミラブルゴム、加熱硬化型液状ゴム等が使用される。そして、これらのゴムの架橋機構として、有機過酸化物架橋、付加反応架橋がある。特に、柔軟性に優れた加熱硬化型ミラブルゴムを有機過酸化物架橋したものが好ましい。
このような構成の管状体1は以下の手順により形成される。先ず、熱可塑性のフッ素樹脂を内層11とし接着性官能基を有するフッ素樹脂を中間層12とした2層構造の成形体を2軸の押出機により共押出して形成する。次に、2層構造の成形体の外周、即ち中間層12の外周にシリコーン系のゴムを外層13とした3層構造の成形体を単軸の押出機により押出して形成する。そして、3層構造の成形体を恒温槽内で、熱加硫処理して外層13を固化する。以上の手順により管状体1が完成する。なお、2層構造の成形体の共押出し成形、3層構造の成形体の押出し成形、及び3層構造の成形体の熱加硫の各処理は、バッチ処理もしくは連続処理により可能である。
以上のような構成の管状体1によれば、化学的安定性は内層11がフッ素樹脂により形成されているため担保され、物理的耐久性、柔軟性は外層13がシリコーン系のゴムにより形成されているため担保されることになる。そして、従来のプライマ処理やプラズマ処理等の表面処理を内層11の外側に施さなくても、内層11と外層13との間に接着性官能基を有するフッ素樹脂で成る中間層12を内層11と共に共押出しにより介在させているので、内層11と外層13とのピール強度を高めることができる。よって、製造工程が簡易となって工数を低減させることができ、さらには変性PFAという特定の接着性官能基を有する材料により中間層12を形成しているので、大きな接着強度が得られると共に、これまでの煩雑な製造工程を必要とすることなく、容易に製造でき、管状体1のコスト増を抑えることができる。
さらに、中間層12が介在することにより得られる上記ピール強度は、従来の表面処理により得られるピール強度よりも大きくなることが後述する発明者らの実験によって確認されている。よって、管状体1を摺動用途に使用しても内層11と外層13との間に掛かる摺動抵抗による剥離を防止することができ、かかる管状体1を長期間にわたって使用することができる。
次に、以下のように実施例1及び比較例1,2の各管状体を作製し、それぞれのピール強度等について検討した。 Hereinafter, embodiments of the present invention will be described. The embodiments described below do not limit the invention according to the claims, and all the combinations of features described in the embodiments are not necessarily essential to the solution means of the invention. Absent.
1 (A) and 1 (B) are a perspective view and a cross-sectional view taken along line AA showing a laminated structure of an embodiment of a tubular body of the present invention. Thetubular body 1 is a laminated tube or hose, and has a triple structure having an inner layer 11, an intermediate layer 12 coated on the outer periphery of the inner layer 11, and an outer layer 13 coated on the outer periphery of the intermediate layer 12. Is formed. The inner layer 11 is formed of a thermoplastic fluororesin excellent in chemical stability such as chemical resistance, heat resistance, and elution, and the intermediate layer 12 is formed of a fluororesin having an adhesive functional group. Is formed of silicone rubber having excellent physical durability such as flexibility and pressure resistance.
Examples of the thermoplastic fluororesin of the inner layer 11 include tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (PFA), ethylene-tetrafluoroethylene copolymer (ETFE), tetrafluoroethylene-hexafluoropropylene copolymer ( FEP), polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF) and the like are used alone or in combination. In particular, PFA which is excellent in chemical resistance and stress crack resistance and easy to process by melt extrusion is preferable.
As the fluororesin having an adhesive functional group of theintermediate layer 12, PFA (modified PFA) having a hydroxyl group or an acid anhydride group is used.
As the silicone rubber of theouter layer 13, heat curable millable rubber, heat curable liquid rubber, or the like is used. And as a crosslinking mechanism of these rubbers, there are organic peroxide crosslinking and addition reaction crosslinking. In particular, a heat-curing type millable rubber excellent in flexibility is cross-linked with an organic peroxide.
Thetubular body 1 having such a configuration is formed by the following procedure. First, a two-layered molded article having a thermoplastic fluororesin as an inner layer 11 and a fluororesin having an adhesive functional group as an intermediate layer 12 is formed by coextrusion with a biaxial extruder. Next, a three-layered molded body having a silicone rubber outer layer 13 formed on the outer periphery of the two-layered molded body, that is, the outer periphery of the intermediate layer 12 is formed by extrusion using a single screw extruder. Then, the outer layer 13 is solidified by heat vulcanizing the molded article having a three-layer structure in a thermostatic bath. The tubular body 1 is completed by the above procedure. Each process of co-extrusion molding of a two-layer structure molded body, extrusion molding of a three-layer structure molded body, and thermal vulcanization of a three-layer structure molded body can be performed by batch processing or continuous processing.
According to thetubular body 1 configured as described above, chemical stability is ensured because the inner layer 11 is formed of a fluororesin, and physical durability and flexibility are formed of the outer layer 13 of silicone rubber. Will be secured. Then, the intermediate layer 12 made of a fluororesin having an adhesive functional group between the inner layer 11 and the outer layer 13 is formed together with the inner layer 11 without subjecting the outer surface of the inner layer 11 to surface treatment such as conventional primer treatment or plasma treatment. Since they are interposed by coextrusion, the peel strength between the inner layer 11 and the outer layer 13 can be increased. Therefore, the manufacturing process can be simplified and the number of man-hours can be reduced. Furthermore, since the intermediate layer 12 is formed of a material having a specific adhesive functional group called modified PFA, a large adhesive strength can be obtained, It can manufacture easily without requiring the complicated manufacturing process until now, and can suppress the cost increase of the tubular body 1.
Furthermore, it has been confirmed by experiments conducted by the inventors described later that the peel strength obtained by theintermediate layer 12 is greater than the peel strength obtained by the conventional surface treatment. Therefore, even if the tubular body 1 is used for sliding applications, peeling due to sliding resistance applied between the inner layer 11 and the outer layer 13 can be prevented, and the tubular body 1 can be used over a long period of time.
Next, each tubular body of Example 1 and Comparative Examples 1 and 2 was produced as follows, and the peel strength and the like were examined.
第1図(A)、(B)は、本発明の管状体の実施形態の積層構造を示す斜視図及びA−A線断面図である。この管状体1は、積層のチューブもしくはホースであり、内層11と、該内層11の外周に被覆された中間層12と、該中間層12の外周に被覆された外層13とを有する3重構造に形成されている。内層11は、耐薬品性、耐熱性、溶出性等の化学的安定性に優れた熱可塑性のフッ素樹脂で形成され、中間層12は、接着性官能基を有するフッ素樹脂で形成され、外層13は、柔軟性、耐圧性等の物理的耐久性に優れたシリコーン系のゴムで形成されている。
内層11の熱可塑性のフッ素樹脂としては、テトラフルオロエチレン−パーフルオロアルキルビニルエーテル共重合体(PFA)、エチレン−テトラフルオロエチレン共重合体(ETFE)、テトラフルオロエチレン−ヘキサフルオロプロピレンコ共重合体(FEP)、ポリテトラフルオロエチレン(PTFE)、ポリフッ化ビニリデン(PVDF)等の中から単独もしくはこれらの組み合わせが選択して使用される。特に、耐薬品性や耐ストレスクラック性に優れ、溶融押出しによる加工が容易なPFAが好ましい。
中間層12の接着性官能基を有するフッ素樹脂としては、ヒドロキシル基あるいは酸無水物基を有するPFA(変性PFA)が使用される。
外層13のシリコーン系のゴムとしては、加熱硬化型ミラブルゴム、加熱硬化型液状ゴム等が使用される。そして、これらのゴムの架橋機構として、有機過酸化物架橋、付加反応架橋がある。特に、柔軟性に優れた加熱硬化型ミラブルゴムを有機過酸化物架橋したものが好ましい。
このような構成の管状体1は以下の手順により形成される。先ず、熱可塑性のフッ素樹脂を内層11とし接着性官能基を有するフッ素樹脂を中間層12とした2層構造の成形体を2軸の押出機により共押出して形成する。次に、2層構造の成形体の外周、即ち中間層12の外周にシリコーン系のゴムを外層13とした3層構造の成形体を単軸の押出機により押出して形成する。そして、3層構造の成形体を恒温槽内で、熱加硫処理して外層13を固化する。以上の手順により管状体1が完成する。なお、2層構造の成形体の共押出し成形、3層構造の成形体の押出し成形、及び3層構造の成形体の熱加硫の各処理は、バッチ処理もしくは連続処理により可能である。
以上のような構成の管状体1によれば、化学的安定性は内層11がフッ素樹脂により形成されているため担保され、物理的耐久性、柔軟性は外層13がシリコーン系のゴムにより形成されているため担保されることになる。そして、従来のプライマ処理やプラズマ処理等の表面処理を内層11の外側に施さなくても、内層11と外層13との間に接着性官能基を有するフッ素樹脂で成る中間層12を内層11と共に共押出しにより介在させているので、内層11と外層13とのピール強度を高めることができる。よって、製造工程が簡易となって工数を低減させることができ、さらには変性PFAという特定の接着性官能基を有する材料により中間層12を形成しているので、大きな接着強度が得られると共に、これまでの煩雑な製造工程を必要とすることなく、容易に製造でき、管状体1のコスト増を抑えることができる。
さらに、中間層12が介在することにより得られる上記ピール強度は、従来の表面処理により得られるピール強度よりも大きくなることが後述する発明者らの実験によって確認されている。よって、管状体1を摺動用途に使用しても内層11と外層13との間に掛かる摺動抵抗による剥離を防止することができ、かかる管状体1を長期間にわたって使用することができる。
次に、以下のように実施例1及び比較例1,2の各管状体を作製し、それぞれのピール強度等について検討した。 Hereinafter, embodiments of the present invention will be described. The embodiments described below do not limit the invention according to the claims, and all the combinations of features described in the embodiments are not necessarily essential to the solution means of the invention. Absent.
1 (A) and 1 (B) are a perspective view and a cross-sectional view taken along line AA showing a laminated structure of an embodiment of a tubular body of the present invention. The
Examples of the thermoplastic fluororesin of the inner layer 11 include tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer (PFA), ethylene-tetrafluoroethylene copolymer (ETFE), tetrafluoroethylene-hexafluoropropylene copolymer ( FEP), polytetrafluoroethylene (PTFE), polyvinylidene fluoride (PVDF) and the like are used alone or in combination. In particular, PFA which is excellent in chemical resistance and stress crack resistance and easy to process by melt extrusion is preferable.
As the fluororesin having an adhesive functional group of the
As the silicone rubber of the
The
According to the
Furthermore, it has been confirmed by experiments conducted by the inventors described later that the peel strength obtained by the
Next, each tubular body of Example 1 and Comparative Examples 1 and 2 was produced as follows, and the peel strength and the like were examined.
先ず、内層にPFA(ダイキン工業製、P62XP)、中間層12に変性PFA(ダイキン工業製、RAP1RC)を選択し、両者を共押出し成形して内径4.1mm、外径4.4mm、内層の厚さと中間層の厚さの比が10:1となる2層構造の成形体を作成した。
次に、外層に加熱硬化型ミラブルシリコーンゴム(信越化学工業製、KE551−U)と加硫剤(信越化学工業製、C−23)を選択し、両者を100:1の質量比で混練して2層構造の成形体と共に押出し成形して外径6.8mmとなる3層構造の成形体を作成した。
そして、3層構造の成形体を、1次加硫温度140°Cで1時間加熱し、さらに2次加硫温度200°Cで4時間加熱することにより加熱硬化型ミラブルシリコーンゴムを硬化させ、3層構造の管状体を作製した。
[比較例1]
先ず、PFA(ダイキン工業製、P62XP)を押出し成形して内径4.1mm、外径4.4mmとなる1層構造の成形体を作成した。
次に、化学的処理として、フッ素ポリマー表面処理剤(潤工社製、テトラエッチ(登録商標)、ナトリウム・ナフタレン錯体を溶剤に溶かした液体)を使って1層構造の成形体の外周面のみを表面処理した後、メタノール、水、アセトンの順で洗浄し乾燥し、その後に1層構造の成形体の外周面をシリコーンゴム系プライマによりプライマ処理した。
そして、加熱硬化型ミラブルシリコーンゴム(信越化学工業製、KE551−U)と加硫剤(信越化学工業製、C−23)を選択し、両者を100:1の質量比で混練してプライマ処理した1層構造の成形体と共に押出し成形して外径6.8mmとなる2層構造の成形体を作成した。そして、2層構造の成形体を、1次加硫温度140°Cで1時間加熱し、さらに2次加硫温度200°Cで4時間加熱することにより加熱硬化型ミラブルシリコーンゴムを硬化させ、2層構造の管状体を作製した。
[比較例2]
先ず、PFA(ダイキン工業製、P62XP)を押出し成形して内径4.1mm、外径4.4mmとなる1層構造の成形体を作成した。
次に、1層構造の成形体の外周面をシリコーンゴム系プライマによりプライマ処理した。
そして、加熱硬化型ミラブルシリコーンゴム(信越化学工業製、KE551−U)と加硫剤(信越化学工業製、C−23)を選択し、両者を100:1の質量比で混練してプライマ処理した1層構造の成形体と共に押出し成形して外径6.8mmとなる2層構造の成形体を作成した。
そして、2層構造の成形体を、1次加硫温度140°Cで1時間加熱し、さらに2次加硫温度200°Cで4時間加熱することにより加熱硬化型ミラブルシリコーンゴムを硬化させ、2層構造の管状体を作製した。
<ピール強度の評価方法>
管状体を長さ5cm×幅1cmの短冊状に切断し、それを引張試験機(島津製作所製、Autograph AGS−J)に装着し、長さ方向に引張速度50mm/minで引っ張り、強度が安定した値の平均値(N=5)を求めた。
第2図は、実施例1及び比較例1.2の各管状体のピール強度、標準偏差、破壊断面の結果を示す図である。破壊断面は、実施例1及び比較例1,2共に界面であり、これによりピール強度が測定されたことになる。実施例1は内層と外層の間に変性PFAの中間層を用いた場合であるが、ピール強度は11.6Nと高い値を示している。一方、比較例1は内層に化学的表面処理とプライマ処理を施した場合であるが、ピール強度は6.76Nと実施例1に比べて著しく低下しており、さらに比較例2は内層にプライマ処理のみを施した場合であるが、ピール強度は0.00Nとなり、内層と外層は全く接着しておらず実用に適さなかった。このことから、熱可塑性のフッ素樹脂製の内層とシリコーン系のゴム製の外層の間には変性PFA製の中間層を介在させて接着することが積層間の接着性に優れており好ましいといえる。 First, PFA (manufactured by Daikin Industries, P62XP) is selected for the inner layer, and modified PFA (manufactured by Daikin Industries, RAP1RC) is selected for theintermediate layer 12, both of which are co-extruded and molded to have an inner diameter of 4.1 mm, an outer diameter of 4.4 mm, A molded article having a two-layer structure in which the ratio of the thickness to the thickness of the intermediate layer was 10: 1 was prepared.
Next, heat-curing type millable silicone rubber (manufactured by Shin-Etsu Chemical Co., KE551-U) and a vulcanizing agent (manufactured by Shin-Etsu Chemical Co., Ltd., C-23) are selected for the outer layer, and both are kneaded at a mass ratio of 100: 1. A three-layered molded body having an outer diameter of 6.8 mm was produced by extrusion molding together with a two-layered molded body.
Then, the molded body having a three-layer structure is heated at a primary vulcanization temperature of 140 ° C. for 1 hour, and further heated at a secondary vulcanization temperature of 200 ° C. for 4 hours to cure the thermosetting millable silicone rubber, A tubular body having a three-layer structure was produced.
[Comparative Example 1]
First, PFA (manufactured by Daikin Industries, P62XP) was extruded to form a single-layer molded body having an inner diameter of 4.1 mm and an outer diameter of 4.4 mm.
Next, as a chemical treatment, the surface of only the outer peripheral surface of the single-layer molded body is treated using a fluoropolymer surface treatment agent (manufactured by Junko Co., Ltd., Tetraetch (registered trademark), a liquid obtained by dissolving sodium / naphthalene complex in a solvent) After the treatment, methanol, water, and acetone were washed in order and dried, and then the outer peripheral surface of the single-layer structure was subjected to a primer treatment with a silicone rubber primer.
Then, a heat curable millable silicone rubber (manufactured by Shin-Etsu Chemical Co., KE551-U) and a vulcanizing agent (manufactured by Shin-Etsu Chemical Co., Ltd., C-23) are selected, and both are kneaded at a mass ratio of 100: 1 to be a primer treatment. A two-layered molded product having an outer diameter of 6.8 mm was produced by extrusion molding together with the molded product having the single-layered structure. Then, the two-layered molded body is heated at a primary vulcanization temperature of 140 ° C. for 1 hour, and further heated at a secondary vulcanization temperature of 200 ° C. for 4 hours to cure the thermosetting millable silicone rubber, A two-layered tubular body was produced.
[Comparative Example 2]
First, PFA (manufactured by Daikin Industries, P62XP) was extruded to form a single-layer molded body having an inner diameter of 4.1 mm and an outer diameter of 4.4 mm.
Next, the outer peripheral surface of the molded article having a single layer structure was subjected to a primer treatment using a silicone rubber primer.
Then, a heat curable millable silicone rubber (manufactured by Shin-Etsu Chemical Co., KE551-U) and a vulcanizing agent (manufactured by Shin-Etsu Chemical Co., Ltd., C-23) are selected, and both are kneaded at a mass ratio of 100: 1 to be a primer treatment. A two-layered molded product having an outer diameter of 6.8 mm was produced by extrusion molding together with the molded product having the single-layered structure.
Then, the two-layered molded body is heated at a primary vulcanization temperature of 140 ° C. for 1 hour, and further heated at a secondary vulcanization temperature of 200 ° C. for 4 hours to cure the thermosetting millable silicone rubber, A two-layered tubular body was produced.
<Peel strength evaluation method>
The tubular body is cut into a strip of 5 cm length x 1 cm width, and is attached to a tensile tester (manufactured by Shimadzu Corp., Autograph AGS-J) and pulled in the length direction at a pulling speed of 50 mm / min, and the strength is stable. The average value (N = 5) was determined.
FIG. 2 is a diagram showing the results of peel strength, standard deviation, and fracture cross section of each tubular body of Example 1 and Comparative Example 1.2. The fracture cross section is an interface in both Example 1 and Comparative Examples 1 and 2, and thus the peel strength was measured. In Example 1, an intermediate layer of modified PFA was used between the inner layer and the outer layer, but the peel strength was as high as 11.6 N. On the other hand, Comparative Example 1 is a case where the inner layer is subjected to chemical surface treatment and primer treatment, but the peel strength is 6.76 N, which is significantly lower than that of Example 1, and Comparative Example 2 is a primer on the inner layer. In the case where only the treatment was performed, the peel strength was 0.00 N, and the inner layer and the outer layer were not adhered at all and were not suitable for practical use. From this, it can be said that it is preferable that the intermediate layer made of modified PFA is interposed between the inner layer made of thermoplastic fluororesin and the outer layer made of silicone rubber because of excellent adhesiveness between the layers. .
次に、外層に加熱硬化型ミラブルシリコーンゴム(信越化学工業製、KE551−U)と加硫剤(信越化学工業製、C−23)を選択し、両者を100:1の質量比で混練して2層構造の成形体と共に押出し成形して外径6.8mmとなる3層構造の成形体を作成した。
そして、3層構造の成形体を、1次加硫温度140°Cで1時間加熱し、さらに2次加硫温度200°Cで4時間加熱することにより加熱硬化型ミラブルシリコーンゴムを硬化させ、3層構造の管状体を作製した。
[比較例1]
先ず、PFA(ダイキン工業製、P62XP)を押出し成形して内径4.1mm、外径4.4mmとなる1層構造の成形体を作成した。
次に、化学的処理として、フッ素ポリマー表面処理剤(潤工社製、テトラエッチ(登録商標)、ナトリウム・ナフタレン錯体を溶剤に溶かした液体)を使って1層構造の成形体の外周面のみを表面処理した後、メタノール、水、アセトンの順で洗浄し乾燥し、その後に1層構造の成形体の外周面をシリコーンゴム系プライマによりプライマ処理した。
そして、加熱硬化型ミラブルシリコーンゴム(信越化学工業製、KE551−U)と加硫剤(信越化学工業製、C−23)を選択し、両者を100:1の質量比で混練してプライマ処理した1層構造の成形体と共に押出し成形して外径6.8mmとなる2層構造の成形体を作成した。そして、2層構造の成形体を、1次加硫温度140°Cで1時間加熱し、さらに2次加硫温度200°Cで4時間加熱することにより加熱硬化型ミラブルシリコーンゴムを硬化させ、2層構造の管状体を作製した。
[比較例2]
先ず、PFA(ダイキン工業製、P62XP)を押出し成形して内径4.1mm、外径4.4mmとなる1層構造の成形体を作成した。
次に、1層構造の成形体の外周面をシリコーンゴム系プライマによりプライマ処理した。
そして、加熱硬化型ミラブルシリコーンゴム(信越化学工業製、KE551−U)と加硫剤(信越化学工業製、C−23)を選択し、両者を100:1の質量比で混練してプライマ処理した1層構造の成形体と共に押出し成形して外径6.8mmとなる2層構造の成形体を作成した。
そして、2層構造の成形体を、1次加硫温度140°Cで1時間加熱し、さらに2次加硫温度200°Cで4時間加熱することにより加熱硬化型ミラブルシリコーンゴムを硬化させ、2層構造の管状体を作製した。
<ピール強度の評価方法>
管状体を長さ5cm×幅1cmの短冊状に切断し、それを引張試験機(島津製作所製、Autograph AGS−J)に装着し、長さ方向に引張速度50mm/minで引っ張り、強度が安定した値の平均値(N=5)を求めた。
第2図は、実施例1及び比較例1.2の各管状体のピール強度、標準偏差、破壊断面の結果を示す図である。破壊断面は、実施例1及び比較例1,2共に界面であり、これによりピール強度が測定されたことになる。実施例1は内層と外層の間に変性PFAの中間層を用いた場合であるが、ピール強度は11.6Nと高い値を示している。一方、比較例1は内層に化学的表面処理とプライマ処理を施した場合であるが、ピール強度は6.76Nと実施例1に比べて著しく低下しており、さらに比較例2は内層にプライマ処理のみを施した場合であるが、ピール強度は0.00Nとなり、内層と外層は全く接着しておらず実用に適さなかった。このことから、熱可塑性のフッ素樹脂製の内層とシリコーン系のゴム製の外層の間には変性PFA製の中間層を介在させて接着することが積層間の接着性に優れており好ましいといえる。 First, PFA (manufactured by Daikin Industries, P62XP) is selected for the inner layer, and modified PFA (manufactured by Daikin Industries, RAP1RC) is selected for the
Next, heat-curing type millable silicone rubber (manufactured by Shin-Etsu Chemical Co., KE551-U) and a vulcanizing agent (manufactured by Shin-Etsu Chemical Co., Ltd., C-23) are selected for the outer layer, and both are kneaded at a mass ratio of 100: 1. A three-layered molded body having an outer diameter of 6.8 mm was produced by extrusion molding together with a two-layered molded body.
Then, the molded body having a three-layer structure is heated at a primary vulcanization temperature of 140 ° C. for 1 hour, and further heated at a secondary vulcanization temperature of 200 ° C. for 4 hours to cure the thermosetting millable silicone rubber, A tubular body having a three-layer structure was produced.
[Comparative Example 1]
First, PFA (manufactured by Daikin Industries, P62XP) was extruded to form a single-layer molded body having an inner diameter of 4.1 mm and an outer diameter of 4.4 mm.
Next, as a chemical treatment, the surface of only the outer peripheral surface of the single-layer molded body is treated using a fluoropolymer surface treatment agent (manufactured by Junko Co., Ltd., Tetraetch (registered trademark), a liquid obtained by dissolving sodium / naphthalene complex in a solvent) After the treatment, methanol, water, and acetone were washed in order and dried, and then the outer peripheral surface of the single-layer structure was subjected to a primer treatment with a silicone rubber primer.
Then, a heat curable millable silicone rubber (manufactured by Shin-Etsu Chemical Co., KE551-U) and a vulcanizing agent (manufactured by Shin-Etsu Chemical Co., Ltd., C-23) are selected, and both are kneaded at a mass ratio of 100: 1 to be a primer treatment. A two-layered molded product having an outer diameter of 6.8 mm was produced by extrusion molding together with the molded product having the single-layered structure. Then, the two-layered molded body is heated at a primary vulcanization temperature of 140 ° C. for 1 hour, and further heated at a secondary vulcanization temperature of 200 ° C. for 4 hours to cure the thermosetting millable silicone rubber, A two-layered tubular body was produced.
[Comparative Example 2]
First, PFA (manufactured by Daikin Industries, P62XP) was extruded to form a single-layer molded body having an inner diameter of 4.1 mm and an outer diameter of 4.4 mm.
Next, the outer peripheral surface of the molded article having a single layer structure was subjected to a primer treatment using a silicone rubber primer.
Then, a heat curable millable silicone rubber (manufactured by Shin-Etsu Chemical Co., KE551-U) and a vulcanizing agent (manufactured by Shin-Etsu Chemical Co., Ltd., C-23) are selected, and both are kneaded at a mass ratio of 100: 1 to be a primer treatment. A two-layered molded product having an outer diameter of 6.8 mm was produced by extrusion molding together with the molded product having the single-layered structure.
Then, the two-layered molded body is heated at a primary vulcanization temperature of 140 ° C. for 1 hour, and further heated at a secondary vulcanization temperature of 200 ° C. for 4 hours to cure the thermosetting millable silicone rubber, A two-layered tubular body was produced.
<Peel strength evaluation method>
The tubular body is cut into a strip of 5 cm length x 1 cm width, and is attached to a tensile tester (manufactured by Shimadzu Corp., Autograph AGS-J) and pulled in the length direction at a pulling speed of 50 mm / min, and the strength is stable. The average value (N = 5) was determined.
FIG. 2 is a diagram showing the results of peel strength, standard deviation, and fracture cross section of each tubular body of Example 1 and Comparative Example 1.2. The fracture cross section is an interface in both Example 1 and Comparative Examples 1 and 2, and thus the peel strength was measured. In Example 1, an intermediate layer of modified PFA was used between the inner layer and the outer layer, but the peel strength was as high as 11.6 N. On the other hand, Comparative Example 1 is a case where the inner layer is subjected to chemical surface treatment and primer treatment, but the peel strength is 6.76 N, which is significantly lower than that of Example 1, and Comparative Example 2 is a primer on the inner layer. In the case where only the treatment was performed, the peel strength was 0.00 N, and the inner layer and the outer layer were not adhered at all and were not suitable for practical use. From this, it can be said that it is preferable that the intermediate layer made of modified PFA is interposed between the inner layer made of thermoplastic fluororesin and the outer layer made of silicone rubber because of excellent adhesiveness between the layers. .
本発明に係る管状体は、医薬品製造設備、半導体製造設備、食品製造設備等の配管として特に有効であるが、例えば電子機器等に内蔵された配管としても適用が可能である。
The tubular body according to the present invention is particularly effective as piping for pharmaceutical manufacturing equipment, semiconductor manufacturing equipment, food manufacturing equipment, etc., but can also be applied, for example, as piping built in electronic equipment or the like.
Claims (2)
- 積層構造の管状体において、
熱可塑性のフッ素樹脂で成る内層と、
該内層の外周に被覆された接着性官能基を有するフッ素樹脂で成る中間層と、
該中間層の外周に被覆されたシリコーン系のゴムで成る外層とを有することを特徴とする管状体。 In a tubular body having a laminated structure,
An inner layer made of thermoplastic fluororesin;
An intermediate layer made of a fluororesin having an adhesive functional group coated on the outer periphery of the inner layer;
A tubular body having an outer layer made of silicone rubber coated on the outer periphery of the intermediate layer. - 前記接着性官能基を有するフッ素樹脂は、ヒドロキシル基あるいは酸無水物基を有するテトラフルオロエチレン−パーフルオロアルキルビニルエーテル共重合体であることを特徴とする請求項1に記載の管状体。 The tubular body according to claim 1, wherein the fluororesin having an adhesive functional group is a tetrafluoroethylene-perfluoroalkyl vinyl ether copolymer having a hydroxyl group or an acid anhydride group.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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JP2008-277006 | 2008-10-28 | ||
JP2008277006A JP2010106882A (en) | 2008-10-28 | 2008-10-28 | Tube |
Publications (1)
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WO2010050366A1 true WO2010050366A1 (en) | 2010-05-06 |
Family
ID=42128732
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/JP2009/067872 WO2010050366A1 (en) | 2008-10-28 | 2009-10-08 | Tube |
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JP (1) | JP2010106882A (en) |
TW (1) | TW201022566A (en) |
WO (1) | WO2010050366A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2870210A4 (en) * | 2012-07-03 | 2016-01-27 | 3M Innovative Properties Co | Siloxane-based pipe coatings |
JP2020046047A (en) * | 2018-09-21 | 2020-03-26 | 株式会社トヨックス | Heat-resistant flexible pipe |
JPWO2021149783A1 (en) * | 2020-01-21 | 2021-07-29 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017094807A1 (en) * | 2015-11-30 | 2017-06-08 | 株式会社 潤工社 | Multilayer tube |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001012659A (en) * | 1999-07-02 | 2001-01-16 | Togawa Rubber Co Ltd | Tubular body |
JP2003131509A (en) * | 2001-10-23 | 2003-05-09 | Canon Inc | Roll |
JP2008105401A (en) * | 2006-09-29 | 2008-05-08 | Nichias Corp | Multilayer tube |
-
2008
- 2008-10-28 JP JP2008277006A patent/JP2010106882A/en active Pending
-
2009
- 2009-10-07 TW TW098133980A patent/TW201022566A/en unknown
- 2009-10-08 WO PCT/JP2009/067872 patent/WO2010050366A1/en active Application Filing
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001012659A (en) * | 1999-07-02 | 2001-01-16 | Togawa Rubber Co Ltd | Tubular body |
JP2003131509A (en) * | 2001-10-23 | 2003-05-09 | Canon Inc | Roll |
JP2008105401A (en) * | 2006-09-29 | 2008-05-08 | Nichias Corp | Multilayer tube |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2870210A4 (en) * | 2012-07-03 | 2016-01-27 | 3M Innovative Properties Co | Siloxane-based pipe coatings |
US10053598B2 (en) | 2012-07-03 | 2018-08-21 | 3M Innovative Properties Company | Siloxane-based pipe coatings |
JP2020046047A (en) * | 2018-09-21 | 2020-03-26 | 株式会社トヨックス | Heat-resistant flexible pipe |
JPWO2021149783A1 (en) * | 2020-01-21 | 2021-07-29 | ||
WO2021149783A1 (en) * | 2020-01-21 | 2021-07-29 | 株式会社 潤工社 | Tube and pump using same |
JP7445999B2 (en) | 2020-01-21 | 2024-03-08 | 株式会社潤工社 | Tube and pump using it |
Also Published As
Publication number | Publication date |
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JP2010106882A (en) | 2010-05-13 |
TW201022566A (en) | 2010-06-16 |
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