EP0678112A1 - Rubber compound for electrical rubber mold products - Google Patents

Rubber compound for electrical rubber mold products

Info

Publication number
EP0678112A1
EP0678112A1 EP94906006A EP94906006A EP0678112A1 EP 0678112 A1 EP0678112 A1 EP 0678112A1 EP 94906006 A EP94906006 A EP 94906006A EP 94906006 A EP94906006 A EP 94906006A EP 0678112 A1 EP0678112 A1 EP 0678112A1
Authority
EP
European Patent Office
Prior art keywords
weight
parts
rubber
silicone
electrical
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP94906006A
Other languages
German (de)
English (en)
French (fr)
Inventor
Hiroyuki 1176-6 Chigira Kobayashi
Tomoo Nagaosa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
3M Co
Original Assignee
Minnesota Mining and Manufacturing Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Minnesota Mining and Manufacturing Co filed Critical Minnesota Mining and Manufacturing Co
Publication of EP0678112A1 publication Critical patent/EP0678112A1/en
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/30Sulfur-, selenium- or tellurium-containing compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/02Elements
    • C08K3/04Carbon
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/34Silicon-containing compounds
    • C08K3/36Silica
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K9/00Use of pretreated ingredients
    • C08K9/08Ingredients agglomerated by treatment with a binding agent
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/16Ethene-propene or ethene-propene-diene copolymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions 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
    • C08L27/02Compositions 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
    • C08L27/12Compositions 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
    • C08L27/18Homopolymers or copolymers or tetrafluoroethene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L83/00Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L91/00Compositions of oils, fats or waxes; Compositions of derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2312/00Crosslinking
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/02Organic macromolecular compounds, natural resins, waxes or and bituminous materials
    • C08L2666/04Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof

Definitions

  • the present invention relates to a rubber molding composition for an electrical appliance excelling in weatherability, elongation, insulation, and resistance to tearing and permitting outdoor use.
  • the material for formed electrical rubber appliances is required to excel in weatherability, elongation, insulation, track resistance, and resistance to tearing.
  • a material which has an ethylene- propylene-diene terpolymer as a main component thereof and satisfies this requirement has not yet been known in the art.
  • the term "PST” means a coating tube which, for the purpose of imparting water resistance and electrical insulation to a joint of connected parts, assumes initially the form of a radially expanded tubular member. The stated qualities are imparted by first being stretched around the joint and subsequently being shrunken to form a strong coat on the joint by dint of the force of the shrinkage.
  • Silicone rubber excels in weatherability, resistance to cold, and resistance to heat but suffers from such drawbacks as low resistance to tearing and high cost.
  • the silicone-modified EPDM excels in resistance to cold, weatherability, and resistance to heat and has found utility in electrical appliances using a rubber molding composition. It nevertheless suffers from inferior resistance to tearing. This drawback gains in prominence particularly in applications that are in need of high elongation.
  • the present invention aims to provide a novel rubber molding composition for electrical appliances, particularly a rubber molding composition suitable for use in a PST, and a PST made therefrom, comprising a silicone- modified EPDM inherently possessing resistance to cold, weatherability, and resistance to heat and surprisingly, improved resistance to tearing.
  • the present inventors have made various studies in search of a solution for the problems mentioned above and consequently found that the silicone-modified EPDM is improved in resistance to tearing by incorporation therein of granular polytetrafluoroethylene and molybdenum disulfide in a small total amount and further improved in resistance to tearing by additional incorporation therein of a 1,4-hexadiene type EPDM of high Mooney viscosity.
  • the present invention has been perfected as a result.
  • the present invention provides a rubber molding composition for electrical appliances comprising (1) 100 parts by weight of a silicone-modified ethylene-propylene-diene terpolymer and (2) from 0.5 to 2 parts by weight of granular polytetrafluoroethylene and an amount of molybdenum disulfide effective to uniformly mix the granular polytetrafluoroethylene with the terpolymer.
  • the present invention also provides a rubber molding composition for electrical appliances comprising (1) 100 parts by weight of a silicone-modified ethylene-propylene-diene terpolymer, (2) from 0.5 to 2 parts by weight of granular polytetrafluoroethylene and such an amount of molybdenum disulfide effective to uniformly mix the granular polytetrafluoroethylene with the terpolymer, and (3) 4 to 20 parts by weight of a 1,4-hexadiene type ethylenepropylene-diene terpolymer possessing a Mooney viscosity, [ML (1+4) 121°C], in the range of from 60 to 80.
  • the present invention provides electrical rubber appliances such as, for example, a pre-stretched tube (PST) , which is formed of the composition mentioned above.
  • PST pre-stretched tube
  • the silicone-modified EDPM to be used in the present invention is the product of a combination of EDPM with polysiloxane and is disclosed in Japanese Unexamined Patent Publications No. 71,737/1980 and No. 116,739/1981. It is marketed by Japan Synthetic Rubber Co., Ltd. under trademark designation of "JENIX-E.”
  • the present invention therefore, can be worked by the use of the commercially available silicone-modified EPDM.
  • the granular polytetrafluoroethylene and an amount of the molybdenum disulfide effective uniformly mix the granular polytetrafluoroethylene with the silicone— modified EPDM constitutes a mixture of 25 to 50 parts by weight of polytetrafluoroethylene with about 1 to 30 parts by weight of molybdenum disulfide. It is disclosed in National Unexamined Patent Publication No. 501,726/1988 (WO87/035151) , for example. This composition is commercially available from Allphaflex Industries, Inc., U.S. under the trademark designation of "Alphaflex ( ⁇ -Flex)."
  • this composition is used in a range of from 0.5 to 2 parts by weight, based on 100 parts by weight of the silicone-modified EPDM. If the amount is less than 0.5 part by weight, the resistance to tearing cannot be sufficiently improved. If the amount exceeds 2 parts by weight, the tensile stress (modulus) at an elongation of from 100% to 300% is too high and the permanent elongation is too inferior for the produced rubber molding composition to serve as a desirable material for the PST.
  • the aforementioned granular polytetrafluoroethylene composition such as, for example, " ⁇ -Flex", and 1,4-hexadiene type EPDM having a Mooney viscosity, [ML (1+4) 121°C) in the range of from 60 to 80 are used in a range of from 0.5 to 3 parts by weight, based on 100 parts by weight of the silicone-modified EPDM.
  • the mixture of the granular polytetrafluoroethylene with the molybdenum disulfide is the same as mentioned above. If the amount of this mixture is less than 0.5 part by weight, based on 100 parts by weight, the product does not acquire sufficient resistance to tearing. If this amount exceeds 3 parts by weight, the modulus at an elongation in the range of from 100 to 300% is likewise too large for the produced rubber molding composition to serve as a desirable material for the PST.
  • the aforementioned 1,4-hexadiene type EPDM having a Mooney viscosity in the range of from 60 to 80 is commercially available from DuPont under the trademark designation of NordelTM.
  • this EPDM is desired to be incorporated in the form of a compound in the silicone-modified EPDM.
  • the amount of this compound to be used is in the range of from 5 to 50 parts by weight (including 1.9 to 19 parts by weight of the 1,4-hexadiene type EPDM of high Mooney viscosity) , based on 100 parts weight of the silicone-modified EPDM. If the amount of the compound is less than 5 parts by weight, no effect is observed in the improvement of mechanical properties. Conversely, if this amount exceeds 50 parts by weight, the EPDM content increases to the extent of degrading the resistance to ultraviolet light.
  • composition of the present invention can incorporate therein such additive components of popular use in the art as carbon black, antioxidant, ultraviolet absorbent, photostabilizer, and cross-linking agent.
  • the composition of the present invention is obtained by mixing the components described above.
  • the production of a formed electrical appliance contemplated by this invention is accomplished by heating the composition as held in a prescribed mold to a temperature in the range of from 130 to 190°C under a pressure in the range of from 15 to 50 kgf/cm 2 for a period in the range of from 5 to 30 minutes.
  • the present invention vests the produced rubber molding composition with high elongation, high resistance to tearing, low permanent elongation, and excellent resistance to ultraviolet light.
  • it provides a rubber molding composition that is suitable for use in electrical appliances, particularly the PST.
  • the product of the present invention finds utility in outdoor rubber products such as, for example, outdoor terminals and insulating covers that require ultraviolet- resisting properties, products such as, for example, the PST for use in the cold climates which requires shrinkage at low temperatures, products such as, for example, a rubber insulating sheath for the PST type terminal
  • Example 1 Test sheets measuring 150 mm x 150 mm x 2 mm were produced by combining 100 parts by weight of a silicone- modified EPDM (produced by Japan Synthetic Rubber Co. , Ltd. and marketed under trademark designation of "JENIX-E2151”) , 5 parts by weight of a cross-linking agent (produced by Hercules Fareast K.K. and marketed under' trademark designation of "VALVUP 40KE”) , and varying amounts indicated in Table 1 of a mixture of granular polytetrafluoroethylene with molybdenum disulfide (produced by Alphaflex Industries, Inc. U.S. and marketed under trademark designation of " ⁇ -Flex 101”) and subjecting the resultant compositions to hot compression molding at 170°C under 25 kgf/cm 2 for 15 minutes.
  • a silicone- modified EPDM produced by Japan Synthetic Rubber Co. , Ltd. and marketed under trademark designation of "JENIX-E2151
  • a cross-linking agent produced by Hercules Fareast K.
  • the samples were tested for hardness, 100% modulus, 300% modulus, tensile strength, resistance to tearing, and permanent elongation as follows.
  • JIS Japanese Industrial Standard
  • the moduli, resistance to tearing, and elongation were determined by preparing dumbbells of JIS No. 3 from the samples, setting them on a tensile tester, and stretching them at a rate of 500 mm/min under the conditions for relevant measurement.
  • the permanent elongation was determined by preparing dumbbells of No. 1 from the samples, keeping them at an elongation of 100% at 100°C for 22 hours, then allowing them to stand at rest at normal room temperature for 30 minutes, removing the cooled dumbbells from the jig, and measuring the lengths thereof.
  • the tear strength was determined by preparing test pieces in the form of a strip 25mm in width and 100 mm in length from the samples, inserting a 50 mm cut in the longitudinal direction in the central part of the test pieces, and measuring the maximum tearing strength of each test piece.
  • Example 2 Test sheets were prepared and tested by following the procedure of Example 1, excepting compositions of 100 parts by weight of a silicone-modified EPDM (produced by Japan Synthetic Rubber Co., Ltd. and marketed under the trademark designation of "JENIX E2151”) , 5 parts by weight of a cross-linking agent (produced by Hercules Fareast K.K. and marketed under the trademark designation of "VALCUP 40KE”) , varying amounts indicated in the following table of a mixture of granular polytetrafluoroethylene with molybdenum disulfide (produced by Alphaflex Industries, Inc. U.S.
  • ⁇ -Flex 101 varying amounts indicated in the following table of a high-Mooney viscosity 1,4-dihexadiene type EPDM (produced by DuPont and marketed under the trademark designation of Nordel 1470”), 0.7 part by weight of an ultraviolet absorbent (produced by Ciba
  • PST samples were prepared by forcing each composition through an extruding device thereby obtaining a hollow cylindrical tube 13.5 mm in its inside diameter and 4 mm in wall thickness, cross-linking the composition forming the hollow cylindrical tube with steam, cutting the cross-linked cylindrical tube into lengths of 75 mm, and fitting the cylindrical tube on a cable in such a manner that the maximum inside diameter thereof would undergo elongation to 225%.
  • the samples thus obtained were tested for crack resistance by the use of a sunshine weather meter produced by Suga Shikenki K.K. under the following conditions: 120 minutes of cycle time, 18 minutes of rainfall, and 63°C of black panel temperature. The results are shown in Table 2 below.
  • the effect in improving resistance to tearing was present when the amount of high-Mooney viscosity 1,4 HD type EPDM was in the range of from 4 to 20 parts by weight and the amount of ⁇ -Flex was in the range of from 0.5 to 3.0 parts by weight. Virtually no improvement in either elongation or moduli was observed when the amount of high-Mooney 1,4 HD type EPDM was 2 parts by weight or less. The UV resistance was adversely affected when this amount was 20 parts by weight or more.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Insulating Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
EP94906006A 1993-01-06 1994-01-03 Rubber compound for electrical rubber mold products Ceased EP0678112A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP5000561A JPH06223629A (ja) 1993-01-06 1993-01-06 電気用ゴム成形組成物
JP561/93 1993-01-06
PCT/US1994/000064 WO1994016011A1 (en) 1993-01-06 1994-01-03 Rubber compound for electrical rubber mold products

Publications (1)

Publication Number Publication Date
EP0678112A1 true EP0678112A1 (en) 1995-10-25

Family

ID=11477141

Family Applications (1)

Application Number Title Priority Date Filing Date
EP94906006A Ceased EP0678112A1 (en) 1993-01-06 1994-01-03 Rubber compound for electrical rubber mold products

Country Status (6)

Country Link
EP (1) EP0678112A1 (enExample)
JP (1) JPH06223629A (enExample)
CN (1) CN1116430A (enExample)
CA (1) CA2151132A1 (enExample)
TW (1) TW251308B (enExample)
WO (1) WO1994016011A1 (enExample)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6100239B2 (ja) * 2012-03-19 2017-03-22 住友化学株式会社 ゴム組成物を用いたロール成型品
CN109679232B (zh) * 2018-12-24 2021-06-22 江阴海达橡塑股份有限公司 一种低温下变形能快速恢复的橡胶
CN120248479B (zh) * 2025-06-05 2025-08-22 安徽赛科思橡胶有限公司 一种低摩擦系数高耐磨的epdm材料及其制备方法

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5571737A (en) * 1978-11-21 1980-05-30 Toshiba Silicone Co Ltd Heat-resistant composition
JPH0721113B2 (ja) * 1985-08-30 1995-03-08 アルファフレックス インダストリーズ インコーポレーテッド エラストマーptfe組成物およびその製法
CA1338292C (en) * 1985-12-09 1996-04-30 William Everett Peters Elastomer ptfe composition, articles, and manufacturing methods

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9416011A1 *

Also Published As

Publication number Publication date
JPH06223629A (ja) 1994-08-12
CA2151132A1 (en) 1994-07-21
CN1116430A (zh) 1996-02-07
WO1994016011A1 (en) 1994-07-21
TW251308B (enExample) 1995-07-11

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