WO2023234124A1 - Ruban protecteur de liaison - Google Patents

Ruban protecteur de liaison Download PDF

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Publication number
WO2023234124A1
WO2023234124A1 PCT/JP2023/019198 JP2023019198W WO2023234124A1 WO 2023234124 A1 WO2023234124 A1 WO 2023234124A1 JP 2023019198 W JP2023019198 W JP 2023019198W WO 2023234124 A1 WO2023234124 A1 WO 2023234124A1
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Prior art keywords
base material
protective tape
binding
parts
mass
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PCT/JP2023/019198
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English (en)
Japanese (ja)
Inventor
洋亮 楯
学 三浦
莉緒 鈴木
大輔 吉村
水貴 蓮見
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デンカ株式会社
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Publication of WO2023234124A1 publication Critical patent/WO2023234124A1/fr

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00—Use of inorganic substances as compounding ingredients
    • C08K3/01—Use of inorganic substances as compounding ingredients characterized by their specific function
    • C08K3/013—Fillers, pigments or reinforcing additives
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • 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
    • C08L27/04—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 chlorine atoms
    • C08L27/06—Homopolymers or copolymers of vinyl chloride
    • 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
    • C08L83/00—Compositions 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
    • C08L83/04—Polysiloxanes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J7/00—Adhesives in the form of films or foils
    • C09J7/20—Adhesives in the form of films or foils characterised by their carriers
    • C09J7/22—Plastics; Metallised plastics
    • C09J7/24—Plastics; Metallised plastics based on macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds

Definitions

  • the present invention relates to a binding protective tape.
  • the binding protective tape can be suitably used for binding and protecting high-voltage cables for electric vehicles and hybrid vehicles, wire harnesses for automobiles, and the like.
  • Patent Documents 1 and 2 Polyvinyl chloride-based binding and protective tapes are used that have a base material made of polyvinyl chloride resin coated with an adhesive on one side. It is also known that the cuttability and abrasion resistance of polyvinyl chloride binding and protective tape can be improved by arranging hard wire rods that are harder than polyvinyl chloride resin in a predetermined cutting direction and embedding them in the base material. (Patent Document 3).
  • An object of the present invention is to provide a binding protective tape that has an excellent balance between flexibility and protective performance, and also has excellent tape storage stability.
  • the base material contains a polyvinyl chloride resin, a plasticizer, a filler, and
  • a sliding property-imparting agent By containing a sliding property-imparting agent and setting the content of the sliding property-imparting agent to 1 to 10 parts by mass based on 100 parts by mass of the polyvinyl chloride resin, the tape has an excellent balance between flexibility and protective performance. It has been found that a binding protective tape with excellent storage stability can be obtained.
  • a binding protective tape comprising a base material and an adhesive layer formed on one side of the base material
  • the base material is composed of a resin composition containing a polyvinyl chloride resin, a plasticizer, a filler, and a slidability imparting agent,
  • the content of the sliding property imparting agent is 1 to 10 parts by mass based on 100 parts by mass of the polyvinyl chloride resin.
  • Binding protection tape [2] Install Nitto Denko Corporation No. 1 on the sample stage.
  • the coefficient of kinetic friction on the surface of the base material is fixed using 5000NS double-sided tape and measured using an R contactor based on ASTM D1894 under the conditions of a load of 200 g and a test speed of 2.5 mm/sec. 0.06 to 0.26, The binding protective tape according to [1].
  • the binding protection tape is fixed to the sample stage via the adhesive layer, and the measurement is performed using an R contactor based on ASTM D1894 under the conditions of a load of 200 g and a test speed of 2.5 mm/sec.
  • the dynamic friction coefficient of the back surface of the base material of the binding protective tape is 0.13 to 0.60.
  • the slidability imparting agent is one selected from the group consisting of linear polyorganosiloxane, crosslinked polyorganosiloxane, silica, talc, glass fiber, and fluororesin. ] to [3].
  • the binding protective tape according to any one of [3].
  • the linear polydimethylsiloxane has a kinematic viscosity of 2,000,000 mm 2 /s or more at 25°C.
  • a binding protective tape that has an excellent balance between flexibility and protective performance, and also has excellent tape storage stability.
  • a binding protective tape according to an embodiment of the present invention includes a base material and an adhesive layer formed on one side of the base material. Each configuration will be described in detail below.
  • the base material according to one embodiment of the present invention contains a polyvinyl chloride resin, a plasticizer, a filler, and a sliding property imparting agent, and the content of the sliding property imparting agent is based on 100 parts by mass of the polyvinyl chloride resin. is composed of a resin composition having 1 to 10 parts by mass.
  • the polyvinyl chloride resin in one embodiment of the present invention preferably has an average degree of polymerization of 1000 to 1500, and two or more types of polyvinyl chloride resins having different average degrees of polymerization may be used. If the average degree of polymerization is less than 1000, sufficient strength (wear resistance) may not be obtained due to insufficient entanglement of polymer chains. If the average degree of polymerization is higher than 1500, gelation may be difficult and film forming properties may deteriorate.
  • the plasticizer in one embodiment of the present invention is not particularly limited as long as it can impart flexibility to the base material.
  • examples include trimellitic acid esters, adipic acid esters, phthalic acid esters, epoxy plasticizers, isophthalic acid esters, terephthalic acid esters, and phosphoric acid plasticizers. From the viewpoint of plasticizing effect on polyvinyl chloride resin and low bleed-out, phthalate esters are preferred. These plasticizers may be used alone or in combination of two or more.
  • phthalate ester plasticizer examples include DINP (diisononyl phthalate), DHP (diheptyl phthalate), DOP (di-2-ethylhexyl phthalate), and n-DOP (diisononyl phthalate). -n-octyl) and diisodecyl phthalate (DIDP).
  • phthalic acid and carbon atoms of 9 to 10 such as DINP (diisononyl phthalate) and diisodecyl phthalate (DIDP), are recommended. Diesters with alcohols are preferred. These plasticizers may be used alone or in combination of two or more.
  • the content of the plasticizer is preferably 38 to 60 parts by weight, more preferably 40 to 50 parts by weight based on 100 parts by weight of the polyvinyl chloride resin. Specifically, for example, it is preferably 38, 40, 42, 43, 44, 45, 46, 48, 50, 55, or 60 parts by mass, and within the range between any two of the numerical values exemplified here. It may be.
  • the plasticizer in an amount of 38 parts by mass or more, the flexibility of the base material is improved and, for example, it is possible to reduce the occurrence of floating in the binding protection tape by improving the followability when it is wound around an electric wire or the like.
  • the wear resistance of the base material can be improved and good protective performance can be obtained.
  • the content of the plasticizer means the total amount of the plasticizer used in combination.
  • the filler in one embodiment of the present invention is not particularly limited as long as it can increase the amount of the base material and improve the hardness.
  • inorganic fillers are preferred from the viewpoint of achieving both a reinforcing effect and flexibility.
  • Examples of the inorganic filler in an embodiment of the present invention include calcium carbonate, aluminum hydroxide, magnesium hydroxide, zirconium hydroxide, calcium hydroxide, potassium hydroxide, barium hydroxide, triphenyl phosphite, and ammonium polyphosphate.
  • polyphosphoric acid amide zirconium oxide, magnesium oxide, zinc oxide, titanium oxide, molybdenum oxide, guanidine phosphate, hydrotalcite, smectite, zinc borate, zinc borate anhydride, zinc metaborate, barium metaborate, antimony oxide, pentoxide
  • examples include antimony, red phosphorus, alumina, boehmite, bentonite, sodium silicate, calcium silicate, calcium sulfate, magnesium carbonate, and carbon black. From the viewpoint of both reinforcing effect and flexibility, calcium carbonate and carbon black are preferred. These fillers may be used alone or in combination of two or more.
  • the content of the filler is preferably 10 to 60 parts by weight, more preferably 20 to 40 parts by weight, based on 100 parts by weight of the polyvinyl chloride resin. Specifically, for example, it is 10, 15, 20, 25, 30, 35, 40, 45, 50, or 60 parts by mass, and may be within a range between any two of the numerical values exemplified here. .
  • the filler in an amount of 10 parts by mass or more, the wear resistance of the base material can be improved and good protective performance can be obtained.
  • the amount of the filler By controlling the amount of the filler to 60 parts by mass or less, the flexibility of the base material is improved and, for example, it is possible to reduce the occurrence of floating in the binding protective tape due to the improved followability when it is wound around electric wires or the like.
  • the content of the filler means the total amount of the filler used together.
  • the sliding properties imparting agent in one embodiment of the present invention is not particularly limited as long as it can impart sliding properties to the base material.
  • Examples include polyorganosiloxane, silica, talc, glass fiber, fluororesin, boron nitride, molybdenum disulfide, ultra-high molecular weight polyethylene resin, and the like. From the viewpoint of achieving both slidability and flexibility, polyorganosiloxane is preferred.
  • the polyorganosiloxane include linear polyorganosiloxane, crosslinked polyorganosiloxane, and the like. These slidability imparting agents may be used alone or in combination of two or more.
  • the slidability imparting agent must be uniformly dispersed in the resin composition from the viewpoint of slidability and prevention of plate-out (a phenomenon in which a part of the resin composition separates and adheres to the molding machine). is preferred.
  • the polyorganosiloxane in one embodiment of the present invention is not particularly limited as long as it has a polyorganosiloxane structure.
  • the polyorganosiloxane structure is a polymer having -Si-O- repeating units in the main chain and organic groups in the side chains. Examples of the repeating unit include those represented by the following structural formula.
  • R 1 and R 2 are each independently an organic group selected from an alkyl group, a polyoxyalkylene group, a fluorine-containing group, and a chlorophenyl group. From the viewpoint of slidability, an alkyl group is preferred. Examples of the alkyl group include a methyl group and an ethyl group from the viewpoint of slidability. These polyorganosiloxane structures may be used alone or in combination of two or more types.
  • the polyorganosiloxane in one embodiment of the present invention may be a linear polyorganosiloxane in which siloxane bonds in the main chain are linearly bonded.
  • Examples of the linear polyorganosiloxane include linear polydimethylsiloxane, linear polymethylphenylsiloxane, and linear polymethylhydrogensiloxane. From the viewpoint of sliding properties, linear polydimethylsiloxane is preferred. These other linear polyorganosiloxanes may be used alone or in combination of two or more types.
  • the kinematic viscosity at 25° C. of the linear polyorganosiloxane is preferably 2 million mm 2 /s or more, more preferably 5 million mm 2 /s or more.
  • the upper limit of the kinematic viscosity is not particularly limited, but from the viewpoint of ease of handling and dispersibility, it is preferably 50 million mm 2 /s or less. Specifically, for example, it is 2 million, 5 million, 15 million, 20 million, 25 million, 30 million, 40 million, or 50 million mm 2 /s, and between any two of the numerical values exemplified here. It may be within the range.
  • the kinematic viscosity at 25° C. of the linear polyorganosiloxane is a value measured by, for example, a kinematic viscometer.
  • the kinematic viscosity of linear polyorganosiloxane can be controlled by adjusting the molecular weight.
  • the kinematic viscosity at 25 ° C. of the linear polyorganosiloxane means the average kinematic viscosity when the linear polyorganosiloxane used together is combined. do.
  • the polyorganosiloxane in one embodiment of the present invention may have a structure in which linear polyorganosiloxane is crosslinked, or a structure in which siloxane bonds are crosslinked in a three-dimensional network. From the viewpoint of sliding properties, polyorganosiloxanes in which linear polyorganosiloxanes are crosslinked are preferred. These crosslinked polyorganosiloxanes may be used alone or in combination of two or more types.
  • the slidability imparting agent in one embodiment of the present invention may be silica, talc, glass fiber, fluororesin, or the like.
  • the content of the sliding properties imparting agent is 1 to 10 parts by weight, more preferably 3 to 7 parts by weight, based on 100 parts by weight of the polyvinyl chloride resin. Specifically, it is, for example, 1, 2, 4, 6, 8, or 10 parts by mass, and may be within a range between any two of the numerical values exemplified here.
  • the content of the slidability imparting agent By setting the content of the slidability imparting agent to 1 part by mass or more, the wear resistance of the base material can be improved and good protective performance can be obtained.
  • the content of the sliding property imparting agent means the total amount of the sliding property imparting agent used together.
  • the resin composition in this embodiment may contain other additives such as colorants, stabilizers, antioxidants, ultraviolet absorbers, lubricants, etc., as necessary, within the range that does not impede the effects of the present invention. can.
  • the thickness of the base material of the binding protective tape in this embodiment varies depending on the intended use and application, but is preferably 180 to 330 ⁇ m, more preferably 180 to 250 ⁇ m. Specifically, for example, it is 180, 185, 190, 195, 200, 205, 210, 220, 250, 280, 300, or 330 ⁇ m, and is within the range between any two of the numerical values exemplified here. It's okay.
  • the base material thickness By setting the base material thickness to 180 ⁇ m or more, the wear resistance of the base material can be improved and good protection performance can be obtained.
  • the thickness of the base material By setting the thickness of the base material to 330 ⁇ m or less, the flexibility of the base material is improved, and for example, it is possible to reduce the occurrence of floating in the binding protective tape due to the improved followability when it is wound around an electric wire or the like.
  • the structure of the base material of the binding protective tape in this embodiment is preferably a single-layer structure from the viewpoint of simplifying the manufacturing process and manufacturing equipment.
  • the resin composition for manufacturing the base material according to this embodiment includes a polyvinyl chloride resin, a plasticizer, a filler, a sliding property imparting agent, and, if necessary, a heat stabilizer, a light absorber, and a pigment. It can be obtained by melting and kneading other additives.
  • the melt-kneading method is not particularly limited, but various mixers and kneaders equipped with heating devices such as twin-screw extruders, continuous and batch-type kneaders, rolls, and Banbury mixers can be used.
  • the materials are mixed so as to be uniformly dispersed, and the resulting mixture is molded into a base material by a conventional molding method such as a calendar method, a T-die method, or an inflation method.
  • a calendar molding machine is preferable from the viewpoint of productivity, color change, uniformity of shape, etc.
  • the roll arrangement method in calender molding may be a known method such as an L-shape, an inverted L-shape, or a Z-shape, and the roll temperature is usually set at 150 to 200°C, preferably 155 to 190°C.
  • the base material is manufactured by Nitto Denko Corporation.
  • the dynamic friction coefficient of the base material surface is 0.0, measured using an R contactor based on ASTM D1894 at a load of 200 g and a test speed of 2.5 mm/sec. It is preferably from 0.06 to 0.26, more preferably from 0.10 to 0.25. Specifically, for example, 0.06, 0.08, 0.10, 0.12, 0.14, 0.16, 0.18, 0.20, 0.22, 0.24, or 0. 26, and may be within the range between any two of the numerical values exemplified here.
  • the dynamic friction coefficient of the base material surface By setting the dynamic friction coefficient of the base material surface to 0.06 or more, the flexibility of the binding protection tape is improved, and for example, when it is wrapped around electric wires, the following properties are improved and the occurrence of lifting of the binding protection tape is reduced. can.
  • the dynamic friction coefficient of the base material surface By setting the dynamic friction coefficient of the base material surface to 0.26 or less, the abrasion resistance of the binding protective tape can be improved and good protective performance can be obtained.
  • the coefficient of dynamic friction on the surface of the base material can be controlled by adjusting the type and content of the slidability imparting agent contained in the resin composition used to manufacture the base material.
  • the dynamic friction coefficient of the base material surface of the base material according to the present embodiment can be measured by the following procedure using, for example, an automatic friction and wear analyzer TS-501 manufactured by Kyowa Interface Science Co., Ltd.
  • the base material sample is cut to a width of 50 mm and a length of 100 mm, and fixed to the sample stage using double-sided tape (No. 5000NS manufactured by Nitto Denko Corporation).
  • An R contactor based on ASTM D1894 is placed on the back surface of the bonded base material sample, and the dynamic friction coefficient is measured under the conditions of a load of 200 g and a test speed of 2.5 mm/sec (room temperature: 23° C., humidity: 50% RH).
  • the tensile modulus in terms of thickness of the base material is preferably 5 to 9 N/mm, more preferably 6 to 9 N/mm. Specifically, it is, for example, 5, 6, 7, 8, or 9 N/mm, and may be within a range between any two of the numerical values exemplified here.
  • the tensile modulus of elasticity converted to the thickness of the base material By setting the tensile modulus of elasticity converted to the thickness of the base material to 9 N/mm or less, the flexibility of the base material is improved, and for example, when wrapped around electric wires, etc., the binding protection tape will not float due to improved followability. can be reduced.
  • the tensile modulus of elasticity converted to the thickness of the base material can be controlled by adjusting the type and content of the slidability imparting agent contained in the resin composition used for manufacturing the base material.
  • the thickness-converted tensile modulus of the base material according to the present embodiment can be obtained from the value of the tensile modulus by the following procedure.
  • a binding tape test piece with a width of 19 mm and a length of 200 mm is clamped and fixed between the chuck parts of a tensile tester so that the distance between the chucks is 100 mm.
  • the test piece is pulled at a speed of 300 mm/min at a room temperature of 23° C. and a relative humidity of 50% RH to measure tensile stress and strain.
  • the ratio of tensile stress to strain between 0.01 and 0.05% strain is calculated by linear regression, and the value is defined as the tensile modulus.
  • the product of the tensile elastic modulus thus obtained and the tape total thickness (unit: mm) is defined as the tensile elastic modulus converted to thickness.
  • the adhesive in the adhesive layer of the binding protective tape according to this embodiment is preferably a rubber adhesive, and may be either a solvent type or an emulsion type.
  • the rubber-based adhesive preferably contains one or more rubbers selected from natural rubber or synthetic rubber and a tackifying resin, and more preferably a mixture of natural rubber, synthetic rubber, and tackifying resin. preferable.
  • the mixing ratio of the tackifier resin is preferably 50 to 150 parts by mass per 100 parts by mass of the rubber component of the mixture containing natural rubber and synthetic rubber.
  • Examples of the natural rubber and synthetic rubber include natural rubber-methyl methacrylate copolymer latex, styrene-butadiene copolymer, acrylonitrile-butadiene copolymer, methyl methacrylate-butadiene copolymer, and the like. These may be used alone or in combination of two or more.
  • the tackifying resin can be selected in consideration of softening point, compatibility with each component, etc.
  • emulsions such as aromatic hydrocarbon resins may be mentioned. These may be used alone or in combination of two or more.
  • the rubber adhesive can be freely selected from a solvent type and an emulsion type, but an emulsion type that generates less VOC is preferable.
  • the binding protective tape according to the present embodiment may be provided between the base material and the adhesive layer for the purpose of improving the adhesion between the base material and the adhesive layer within a range that does not impede the effects of the present invention.
  • a primer layer may also be provided.
  • the thickness of the undercoat layer is usually 0.1 to 1 ⁇ m, more preferably 0.3 to 0.5 ⁇ m, and the thickness of the undercoat layer is preferably smaller than the thickness of the base material.
  • the undercoat forming the undercoat layer is preferably one consisting of 25 to 300 parts by mass of an acrylonitrile-butadiene copolymer based on 100 parts by mass of a graft polymer obtained by graft polymerizing methyl methacrylate to natural rubber.
  • the graft polymer obtained by graft-polymerizing methyl methacrylate onto natural rubber used in the primer is preferably one in which 70-50 mass % of natural rubber is graft-polymerized with 30-50 mass % methyl methacrylate. If the ratio of methyl methacrylate in the graft polymer is less than 30% by mass, the adhesion between methyl methacrylate and the film base material may deteriorate, and delamination of the binding protective tape may occur. Moreover, if the ratio of methyl methacrylate is more than 50% by mass, the undercoat itself will harden and be unable to follow the deformation of the film base material, which may cause delamination of the binding protective tape.
  • the acrylonitrile-butadiene copolymer used in the primer includes medium nitrile type (acrylonitrile 25-30% by mass, butadiene 75-70% by mass), medium-high nitrile type (acrylonitrile 31-35% by mass, butadiene 69-65% by mass). %) high nitrile type (acrylonitrile 36-43% by mass, butadiene 64-57% by mass). These may be used alone or in combination of two or more.
  • the binding protection tape according to the present embodiment can be produced by, for example, applying an undercoat to one side of a base material, removing the solvent sufficiently in a drying oven, applying an adhesive, and then applying it in a drying oven in the same way as the undercoat. After sufficiently removing the solvent, an adhesive is applied to obtain a binding protective tape.
  • Coating methods for the primer include the gravure method, spray method, kiss roll method, bar method, knife method, etc., and methods for applying the adhesive include the comma method, lip die method, gravure method, and roll method. , slot die method, etc.
  • the thickness of the primer layer is usually 0.1 to 1 ⁇ m, more preferably 0.3 to 0.5 ⁇ m. Further, the thickness of the adhesive layer varies depending on the purpose and application, but is usually 5 to 50 ⁇ m, more preferably 10 to 30 ⁇ m.
  • ⁇ Dynamic friction coefficient on the back side of the binding protective tape base material> an R contactor based on ASTM D1894 is used, a load of 200 g and a test speed of 2.5 mm/sec are used when the binding protection tape is fixed to the measurement stage via an adhesive layer.
  • the dynamic friction coefficient of the back surface of the binding protective tape base material measured under the following conditions is preferably 0.13 to 0.60, more preferably 0.23 to 0.58. Specifically, for example, 0.13, 0.15, 0.20, 0.25, 0.30, 0.35, 0.40, 0.45, 0.50, 0.55, or 0. It is preferably 60, and may be within a range between any two of the numerical values exemplified here.
  • the back surface of the binding protective tape base material means the surface of the binding protective tape base material that is opposite to the surface on which the adhesive layer is formed.
  • the coefficient of dynamic friction on the surface of the base material increases, the coefficient of dynamic friction on the back surface of the base material of the binding protective tape tends to increase as well. Therefore, it can be controlled by adjusting the dynamic friction coefficient of the base material surface within the above-mentioned range.
  • the coefficient of dynamic friction on the back side of the base material of the binding protective tape tends to be a larger value than the coefficient of dynamic friction on the surface of the base material, but due to the above relationship,
  • the coefficient of dynamic friction on the back surface of the base material of the binding protective tape can be controlled within a desired range.
  • the dynamic friction coefficient of the back surface of the binding protective tape base material can be controlled by adjusting the dynamic friction coefficient of the base material surface within the above-mentioned range.
  • the back surface dynamic friction coefficient of the binding protective tape base material in the binding protective tape according to the present embodiment can be measured by the following procedure using, for example, an automatic friction and wear analysis device TS-501 manufactured by Kyowa Interface Science Co., Ltd.
  • the binding protective tape sample is cut into 50 mm width x 100 mm length and fixed to the sample stage via the adhesive layer of the binding protective tape sample.
  • An R contactor based on ASTM D1894 is placed on the back of the bonded protective tape sample, and the dynamic friction coefficient is measured under the conditions of a load of 200 g and a test speed of 2.5 mm/sec (room temperature: 23° C., humidity: 50% RH).
  • the binding protective tape according to the present embodiment is suitably used as a binding protective tape for binding high-voltage cables and wire harnesses of electric vehicles and hybrid vehicles, for example.
  • Linear polydimethylsiloxane (kinematic viscosity 1 million mm 2 /s at 25°C): Product name "AK1000000”, manufactured by Asahi Kasei Wacker Silicone Co., Ltd.
  • Crosslinked polydimethylsiloxane (linear Polyorganosiloxane (crosslinked polyorganosiloxane): Product name "KMP-597", manufactured by Shin-Etsu Chemical Co., Ltd.
  • Silica Product name "HDK H-18", manufactured by Asahi Kasei Wacker Silicone Co., Ltd.
  • Talc Product Glass fiber: Product name: "Himicron HE5", manufactured by Takehara Chemical Industry Co., Ltd.
  • Glass fiber Product name: "Milled fiber EPH80M-10A", manufactured by Nippon Electric Glass Co., Ltd.
  • Fluororesin Product name: "Dyneon PTFE Micro Powder TF9207Z”, manufactured by 3M ( 3) Plasticizer Phthalate ester plasticizer, diisononyl phthalate: Product name "DINP”, manufactured by J-Plus Co., Ltd.
  • Filler Calcium carbonate Product name "Calcease (registered trademark) P", manufactured by Kamishima Chemical Industry Co., Ltd. Manufactured by Co., Ltd.
  • a polyvinyl chloride resin, a sliding property imparting agent, a plasticizer, and a filler were melt-kneaded in the compositions shown in Tables 1 and 2 using a Banbury mixer so as to be uniformly dispersed, and then heated to a roll temperature of 165 using a calendar molding machine.
  • a base material of a predetermined thickness was produced at °C.
  • ⁇ Preparation of binding protective tape> ⁇ Materials used> (1) Base material Base material created by the above process (2) Undercoat layer Mixture emulsion of graft polymer latex obtained by graft polymerizing methyl methacrylate to natural rubber and acrylonitrile butadiene copolymer emulsion: Product name KT4612A, E-Tech Co., Ltd. (3) Adhesive layer made by HA LATEX Co., Ltd.
  • the thickness of the undercoat layer after drying was 0.3 ⁇ m, and the thickness of the adhesive layer after drying was 20 ⁇ m.
  • ⁇ Dynamic friction coefficient of base material surface The measurement was performed using an automatic friction and wear analyzer TS-501 manufactured by Kyowa Interface Science Co., Ltd. according to the following procedure.
  • the base material sample was cut to a width of 50 mm and a length of 100 mm, and was fixed to a sample stage using double-sided tape (No. 5000NS manufactured by Nitto Denko Corporation).
  • An R contactor based on ASTM D1894 was placed on the back surface of the bonded base material sample, and the dynamic friction coefficient was measured under the conditions of a load of 200 g and a test speed of 2.5 mm/sec (room temperature: 23° C., humidity: 50% RH).
  • ⁇ Dynamic friction coefficient of binding protective tape> The measurement was performed using an automatic friction and wear analyzer TS-501 manufactured by Kyowa Interface Science Co., Ltd. according to the following procedure.
  • the binding protective tape sample was cut into 50 mm width x 100 mm length, and was affixed and fixed to a sample stage via an adhesive layer.
  • An R contactor based on ASTM D1894 was placed on the back of the bonded protective tape sample, and the dynamic friction coefficient was measured under the conditions of a load of 200 g and a test speed of 2.5 mm/sec (room temperature: 23° C., humidity: 50% RH).
  • ⁇ Tensile modulus/tensile modulus converted to thickness A binding tape test piece with a width of 19 mm and a length of 200 mm was clamped and fixed between the chuck parts of a tensile testing machine so that the distance between the chucks was 100 mm. The test piece was pulled at a speed of 300 mm/min at a room temperature of 23° C. and a relative humidity of 50% RH, and tensile stress and strain were measured. The ratio of tensile stress to strain between 0.01 and 0.05% strain was calculated by linear regression, and the value was defined as the tensile modulus. Further, the product of the tensile elastic modulus and the total tape thickness (unit: mm) was used as the tensile elastic modulus converted into thickness.
  • the durometer A hardness of the base material samples stacked to a thickness of 6 mm or more was measured using an Asker rubber hardness meter A type (type A indenter based on ASTM D2240) manufactured by Kobunshi Keiki Co., Ltd. (room temperature: 23° C., humidity: 50% RH).
  • Abrasion resistance was evaluated according to the following procedure. It was conducted in accordance with ISO6722-1 (2001). The base material sample was wrapped twice around a cylinder with a diameter of 10 mm and fixed with tape or the like. From above, the surface of the sample was abraded at a speed of 1500 mm/min using sandpaper whose hard material was fused alumina and had a particle size of 150 ⁇ m. The abrasion distance (mm) until a hole appeared in the sample was measured (room temperature: 23° C., humidity: 50% RH). The wear distance (mm) until a hole appeared in the sample was evaluated using the following criteria.
  • a base material with an excellent evaluation of abrasion distance has high abrasion resistance, so it can be expected that excellent protection performance can be achieved in a binding protective tape manufactured using the base material.
  • Wear distance is 1000 mm or more
  • Wear distance is 800 mm or more and less than 1000 mm
  • Wear distance is less than 800 mm
  • the binding protective tape using the base material according to the example and the binding protective tape according to the example have an excellent balance of flexibility and protective performance, and furthermore, the binding protective tape using the base material according to the example Since the material has excellent storage stability, it is expected that a binding protective tape using this base material will have excellent storage stability.
  • the protective binding tape using the base material according to the comparative example is inferior in one or more aspects of the balance between flexibility and protective performance and the storage stability of the protective binding tape.
  • the binding protective tape according to the present invention has an excellent balance between flexibility and protective performance, and also has excellent tape storage stability.
  • the binding protective tape according to the present invention can be suitably used for binding and protecting high-voltage cables for electric vehicles and hybrid vehicles, wire harnesses for automobiles, etc., and has industrial applicability.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Adhesive Tapes (AREA)
  • Adhesives Or Adhesive Processes (AREA)
  • Package Frames And Binding Bands (AREA)

Abstract

L'invention concerne un ruban protecteur de liaison qui présente un excellent équilibre entre la flexibilité et les performances de protection, et présente également une excellente stabilité au stockage de ruban. La présente invention concerne un ruban protecteur de liaison ayant un substrat et une couche adhésive formée sur un côté du substrat, le substrat étant composé d'une composition de résine contenant une résine de polychlorure de vinyle, un plastifiant, une charge et un agent conférant une aptitude au glissement, et la teneur de l'agent conférant une aptitude au glissement dans la composition de résine étant de 1 à 10 parties en masse par rapport à 100 parties en masse de la résine de polychlorure de vinyle.
PCT/JP2023/019198 2022-05-30 2023-05-23 Ruban protecteur de liaison WO2023234124A1 (fr)

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JP2022-087865 2022-05-30

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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08291243A (ja) * 1995-04-21 1996-11-05 Zeon Kasei Co Ltd 粉末成形用塩化ビニル樹脂組成物およびそれを用いた積層体
US6541558B1 (en) * 1996-10-09 2003-04-01 Res Development Corporation Thermoplastic polymers with dispersed fluorocarbon additives
JP3888431B2 (ja) * 2001-11-28 2007-03-07 住友電装株式会社 ワイヤハーネス保護材及びこれを用いたワイヤハーネス
WO2014077280A1 (fr) * 2012-11-13 2014-05-22 矢崎総業株式会社 Composition de résine de polychlorure de vinyle pour fils électriques d'automobile, et fils électriques basse tension ultrafins pour automobile
CN111748162A (zh) * 2020-06-30 2020-10-09 江门市支点光电科技有限公司 一种导热pvc组合物及其制备方法
WO2021029403A1 (fr) * 2019-08-15 2021-02-18 デンカ株式会社 Ruban adhésif

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH08291243A (ja) * 1995-04-21 1996-11-05 Zeon Kasei Co Ltd 粉末成形用塩化ビニル樹脂組成物およびそれを用いた積層体
US6541558B1 (en) * 1996-10-09 2003-04-01 Res Development Corporation Thermoplastic polymers with dispersed fluorocarbon additives
JP3888431B2 (ja) * 2001-11-28 2007-03-07 住友電装株式会社 ワイヤハーネス保護材及びこれを用いたワイヤハーネス
WO2014077280A1 (fr) * 2012-11-13 2014-05-22 矢崎総業株式会社 Composition de résine de polychlorure de vinyle pour fils électriques d'automobile, et fils électriques basse tension ultrafins pour automobile
WO2021029403A1 (fr) * 2019-08-15 2021-02-18 デンカ株式会社 Ruban adhésif
CN111748162A (zh) * 2020-06-30 2020-10-09 江门市支点光电科技有限公司 一种导热pvc组合物及其制备方法

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