RU2401848C2 - Изделие холодной усадки и способ изготовления изделия холодной усадки - Google Patents
Изделие холодной усадки и способ изготовления изделия холодной усадки Download PDFInfo
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- RU2401848C2 RU2401848C2 RU2008103168A RU2008103168A RU2401848C2 RU 2401848 C2 RU2401848 C2 RU 2401848C2 RU 2008103168 A RU2008103168 A RU 2008103168A RU 2008103168 A RU2008103168 A RU 2008103168A RU 2401848 C2 RU2401848 C2 RU 2401848C2
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- Prior art keywords
- epichlorohydrin
- product
- elastomeric
- cold shrink
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- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 description 1
- VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 1
- 229910052754 neon Inorganic materials 0.000 description 1
- GKAOGPIIYCISHV-UHFFFAOYSA-N neon atom Chemical compound [Ne] GKAOGPIIYCISHV-UHFFFAOYSA-N 0.000 description 1
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- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 238000013031 physical testing Methods 0.000 description 1
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- YBBJKCMMCRQZMA-UHFFFAOYSA-N pyrithione Chemical compound ON1C=CC=CC1=S YBBJKCMMCRQZMA-UHFFFAOYSA-N 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000006254 rheological additive Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
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- 239000004945 silicone rubber Substances 0.000 description 1
- 239000012748 slip agent Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
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- 238000007655 standard test method Methods 0.000 description 1
- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 1
- UWHCKJMYHZGTIT-UHFFFAOYSA-N tetraethylene glycol Chemical compound OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 1
- 229920002725 thermoplastic elastomer Polymers 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
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- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Images
Classifications
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C61/00—Shaping by liberation of internal stresses; Making preforms having internal stresses; Apparatus therefor
- B29C61/06—Making preforms having internal stresses, e.g. plastic memory
- B29C61/0608—Making preforms having internal stresses, e.g. plastic memory characterised by the configuration or structure of the preforms
- B29C61/065—Preforms held in a stressed condition by means of a removable support; Supports therefor
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/16—Homopolymers or copolymers or vinylidene fluoride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
- C08L71/03—Polyepihalohydrins
-
- 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
- F16L47/00—Connecting arrangements or other fittings specially adapted to be made of plastics or to be used with pipes made of plastics
- F16L47/20—Connecting arrangements or other fittings specially adapted to be made of plastics or to be used with pipes made of plastics based principally on specific properties of plastics
- F16L47/22—Connecting arrangements or other fittings specially adapted to be made of plastics or to be used with pipes made of plastics based principally on specific properties of plastics using shrink-down material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2019/00—Use of rubber not provided for in a single one of main groups B29K2007/00 - B29K2011/00, as moulding material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C08L27/18—Homopolymers or copolymers or tetrafluoroethene
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Laminated Bodies (AREA)
- Insulating Bodies (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/191,838 | 2005-07-28 | ||
| US11/191,838 US7553894B2 (en) | 2005-07-28 | 2005-07-28 | Cold-shrink article and method of making cold-shrink article |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| RU2008103168A RU2008103168A (ru) | 2009-09-10 |
| RU2401848C2 true RU2401848C2 (ru) | 2010-10-20 |
Family
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2008103168A RU2401848C2 (ru) | 2005-07-28 | 2006-07-27 | Изделие холодной усадки и способ изготовления изделия холодной усадки |
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| Country | Link |
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| US (1) | US7553894B2 (enExample) |
| EP (1) | EP1907475B1 (enExample) |
| JP (1) | JP2009503195A (enExample) |
| KR (1) | KR20080039383A (enExample) |
| CN (1) | CN101233189B (enExample) |
| BR (1) | BRPI0614660A2 (enExample) |
| CA (1) | CA2616640C (enExample) |
| ES (1) | ES2630388T3 (enExample) |
| MX (1) | MX2008001128A (enExample) |
| RU (1) | RU2401848C2 (enExample) |
| TW (1) | TW200712119A (enExample) |
| WO (1) | WO2007016198A1 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7705085B2 (en) * | 2007-04-06 | 2010-04-27 | 3M Innovative Properties Company | Fluoroelastomer composition for cold shrink articles |
| US7642460B2 (en) * | 2007-04-06 | 2010-01-05 | 3M Innovative Properties Company | Cold shrinkable article including a fluoroelastomer composition |
| US20080280080A1 (en) * | 2007-05-07 | 2008-11-13 | Bandyopadhyay Pradip K | Cold shrinkable article including an epichlorohydrin composition |
| US8188178B2 (en) * | 2007-05-07 | 2012-05-29 | 3M Innovative Properties Company | Cold shrinkable article including an epichlorohydrin composition |
| US7635813B2 (en) * | 2007-09-10 | 2009-12-22 | 3M Innovative Properties Company | Article and method for sealing fluid-containing cables |
| US7973241B2 (en) * | 2007-09-10 | 2011-07-05 | 3M Innovative Properties Company | Pressure restraining enclosure for cables |
| US8324502B2 (en) * | 2009-01-19 | 2012-12-04 | Tyco Electronics Corporation | Covered cable assemblies and methods and systems for forming the same |
| US8716600B2 (en) | 2012-04-18 | 2014-05-06 | Tyco Electronics Corporation | Cable connector systems and methods including same |
| US9425605B2 (en) | 2013-03-14 | 2016-08-23 | Tyco Electronics Corporation | Method for protecting a cable splice connection with a cover assembly |
| EP3160738B1 (en) | 2014-06-27 | 2020-04-01 | Dow Global Technologies LLC | Cold shrink article for electrical device |
| EP3228663A4 (en) * | 2014-12-02 | 2018-08-08 | Daikin Industries, Ltd. | Fluorine rubber composition and cross-linked fluorine rubber |
| TWI577870B (zh) * | 2016-03-03 | 2017-04-11 | Chen Jin-Fu | No rope curtain curtain curtain body transmission mechanism |
| US10389103B2 (en) | 2016-10-18 | 2019-08-20 | Te Connectivity Corporation | Breakout boot assemblies and methods for covering electrical cables and connections |
| JP7187925B2 (ja) * | 2018-09-25 | 2022-12-13 | 日本ゼオン株式会社 | エピハロヒドリン系ゴム組成物およびゴム架橋物 |
| CN111391354A (zh) * | 2020-03-13 | 2020-07-10 | 东莞市耐士迪汽车配件有限公司 | 一种硅胶握把套的冷缩安装工艺 |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4188352A (en) * | 1977-12-30 | 1980-02-12 | Daikin Kogyo Co., Ltd. | Elastomeric composition comprising fluoroelastomer and epicholorohydrin elastomer |
| EP0750381A1 (en) * | 1995-06-21 | 1996-12-27 | Minnesota Mining And Manufacturing Company | Crushable core and cover assembly having an expanded elastomeric tubing and a chrushable core |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS606238B2 (ja) | 1981-01-30 | 1985-02-16 | 豊田合成株式会社 | ゴム積層体 |
| SU1024480A1 (ru) | 1981-10-08 | 1983-06-23 | Предприятие П/Я Г-4913 | Вулканизуема резинова смесь |
| US4645801A (en) * | 1982-09-15 | 1987-02-24 | The Bf Goodrich Company | Epihalohydrin polymers |
| JPS6284153A (ja) | 1985-10-09 | 1987-04-17 | Sumitomo Chem Co Ltd | 加硫ゴム組成物 |
| JPH07113076B2 (ja) | 1986-09-24 | 1995-12-06 | 日本ゼオン株式会社 | 耐油性ゴム混合物 |
| JPS6460214A (en) | 1987-08-27 | 1989-03-07 | Furukawa Electric Co Ltd | Manufacture of elastic self-shrinking branch tube |
| DE3731835A1 (de) * | 1987-09-22 | 1989-03-30 | Siemens Ag | Laserstrahl-induziertes farbdrucken |
| JPH01159245A (ja) * | 1987-12-16 | 1989-06-22 | Tokai Rubber Ind Ltd | ゴムホース |
| JPH01294760A (ja) * | 1988-05-23 | 1989-11-28 | Japan Synthetic Rubber Co Ltd | フッ素ゴム組成物および架橋可能なフッ素ゴム組成物 |
| JP2594329B2 (ja) | 1988-07-15 | 1997-03-26 | 電気化学工業株式会社 | 低光沢フツ素樹脂系屋外用フイルムまたはシート及びその製造方法 |
| US5560845A (en) * | 1994-02-28 | 1996-10-01 | E. I. Du Pont De Nemours And Company | Laser marking of fluoropolymer composition |
| AU6767996A (en) * | 1995-09-06 | 1997-03-27 | Minnesota Mining And Manufacturing Company | Epihalohydrin electrical stress controlling material |
| US6114452A (en) * | 1996-11-25 | 2000-09-05 | E. I. Du Pont De Nemours And Company | Perfluoroelastomer composition having excellent heat stability |
| EP1167441B1 (en) * | 2000-06-29 | 2015-07-29 | 3M Innovative Properties Company | Fluoroelastomer composition comprising a mineral oil |
| JP3899830B2 (ja) * | 2001-03-01 | 2007-03-28 | 日立電線株式会社 | ケーブル接続部用常温収縮チューブ及びそれに使用されるゴム組成物 |
| JP2002317885A (ja) | 2001-04-19 | 2002-10-31 | Tokai Rubber Ind Ltd | 金属複合ホースとその製造方法 |
| US20030124285A1 (en) | 2001-12-31 | 2003-07-03 | Hopcus Ernest A. | Removable core for pre-stretched tube |
| US6838512B2 (en) * | 2003-06-05 | 2005-01-04 | 3M Innovative Properties Company | Cold shrink fluoroelastomeric article |
| US20050214491A1 (en) * | 2004-03-23 | 2005-09-29 | 3M Innovative Properties Company | Cold-shrink marker sleeve |
| US20050215661A1 (en) * | 2004-03-23 | 2005-09-29 | 3M Innovative Properties Company | NBC-resistant composition |
| US20050277731A1 (en) * | 2004-06-11 | 2005-12-15 | Shin-Etsu Chemical Co., Ltd. | Curable perfluoropolyether compositions and rubber or gel articles comprising the same |
| US7396499B2 (en) * | 2004-09-28 | 2008-07-08 | Thomas E Frankel | Multiple layered membrane with fluorine containing polymer layer |
-
2005
- 2005-07-28 US US11/191,838 patent/US7553894B2/en active Active
-
2006
- 2006-07-27 WO PCT/US2006/029106 patent/WO2007016198A1/en not_active Ceased
- 2006-07-27 KR KR1020087002043A patent/KR20080039383A/ko not_active Ceased
- 2006-07-27 BR BRPI0614660-0A patent/BRPI0614660A2/pt not_active Application Discontinuation
- 2006-07-27 CA CA 2616640 patent/CA2616640C/en not_active Expired - Fee Related
- 2006-07-27 ES ES06800372.2T patent/ES2630388T3/es active Active
- 2006-07-27 MX MX2008001128A patent/MX2008001128A/es active IP Right Grant
- 2006-07-27 RU RU2008103168A patent/RU2401848C2/ru not_active IP Right Cessation
- 2006-07-27 EP EP06800372.2A patent/EP1907475B1/en not_active Not-in-force
- 2006-07-27 JP JP2008524127A patent/JP2009503195A/ja active Pending
- 2006-07-27 CN CN2006800276053A patent/CN101233189B/zh not_active Expired - Fee Related
- 2006-07-28 TW TW095127827A patent/TW200712119A/zh unknown
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4188352A (en) * | 1977-12-30 | 1980-02-12 | Daikin Kogyo Co., Ltd. | Elastomeric composition comprising fluoroelastomer and epicholorohydrin elastomer |
| EP0750381A1 (en) * | 1995-06-21 | 1996-12-27 | Minnesota Mining And Manufacturing Company | Crushable core and cover assembly having an expanded elastomeric tubing and a chrushable core |
Non-Patent Citations (1)
| Title |
|---|
| КОШЕЛЕВ Ф.Ф. и др. Общая технология резины.- М.: Химия, 1978, с.102. * |
Also Published As
| Publication number | Publication date |
|---|---|
| RU2008103168A (ru) | 2009-09-10 |
| EP1907475A1 (en) | 2008-04-09 |
| WO2007016198A1 (en) | 2007-02-08 |
| ES2630388T3 (es) | 2017-08-21 |
| JP2009503195A (ja) | 2009-01-29 |
| CN101233189B (zh) | 2011-09-28 |
| EP1907475B1 (en) | 2017-04-19 |
| US20070027236A1 (en) | 2007-02-01 |
| US7553894B2 (en) | 2009-06-30 |
| MX2008001128A (es) | 2008-03-13 |
| TW200712119A (en) | 2007-04-01 |
| CN101233189A (zh) | 2008-07-30 |
| CA2616640C (en) | 2013-12-17 |
| KR20080039383A (ko) | 2008-05-07 |
| CA2616640A1 (en) | 2007-02-08 |
| BRPI0614660A2 (pt) | 2011-04-12 |
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| CA2682977C (en) | Fluoroelastomer composition for cold shrink articles | |
| US7642460B2 (en) | Cold shrinkable article including a fluoroelastomer composition | |
| RU2401848C2 (ru) | Изделие холодной усадки и способ изготовления изделия холодной усадки | |
| US20080280080A1 (en) | Cold shrinkable article including an epichlorohydrin composition |
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