USRE23843E - Insulating tape - Google Patents
Insulating tape Download PDFInfo
- Publication number
- USRE23843E USRE23843E US23843DE USRE23843E US RE23843 E USRE23843 E US RE23843E US 23843D E US23843D E US 23843DE US RE23843 E USRE23843 E US RE23843E
- Authority
- US
- United States
- Prior art keywords
- tape
- film
- adhesive
- parts
- pressure
- 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.)
- Expired
Links
- 239000000853 adhesive Substances 0.000 description 40
- 230000001070 adhesive Effects 0.000 description 40
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 25
- 239000011248 coating agent Substances 0.000 description 22
- 238000000576 coating method Methods 0.000 description 22
- 239000000203 mixture Substances 0.000 description 22
- 229920000642 polymer Polymers 0.000 description 19
- 239000004014 plasticizer Substances 0.000 description 16
- 239000000463 material Substances 0.000 description 15
- 229920005989 resin Polymers 0.000 description 13
- 239000011347 resin Substances 0.000 description 13
- 239000002987 primer (paints) Substances 0.000 description 10
- BJQHLKABXJIVAM-UHFFFAOYSA-N Bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 9
- 229920002554 vinyl polymer Polymers 0.000 description 9
- BZHJMEDXRYGGRV-UHFFFAOYSA-N vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 8
- 239000002390 adhesive tape Substances 0.000 description 7
- 239000004020 conductor Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 6
- 238000003490 calendering Methods 0.000 description 5
- 239000000969 carrier Substances 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 229920001971 elastomer Polymers 0.000 description 5
- 238000009413 insulation Methods 0.000 description 5
- 239000003607 modifier Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000005060 rubber Substances 0.000 description 5
- 230000001788 irregular Effects 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N n-heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- 229920000915 polyvinyl chloride Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- HGAZMNJKRQFZKS-UHFFFAOYSA-N chloroethene;ethenyl acetate Chemical compound ClC=C.CC(=O)OC=C HGAZMNJKRQFZKS-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 238000003801 milling Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 235000011837 pasties Nutrition 0.000 description 3
- 239000004800 polyvinyl chloride Substances 0.000 description 3
- 230000002035 prolonged Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 150000003505 terpenes Chemical class 0.000 description 3
- 235000007586 terpenes Nutrition 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- 239000004416 thermosoftening plastic Substances 0.000 description 3
- 239000004408 titanium dioxide Substances 0.000 description 3
- 238000004804 winding Methods 0.000 description 3
- ZNRLMGFXSPUZNR-UHFFFAOYSA-N 2,2,4-trimethyl-1H-quinoline Chemical compound C1=CC=C2C(C)=CC(C)(C)NC2=C1 ZNRLMGFXSPUZNR-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- 229920000180 Alkyd Polymers 0.000 description 2
- 240000008528 Hevea brasiliensis Species 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N Sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 2
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 230000001464 adherent Effects 0.000 description 2
- 230000003078 antioxidant Effects 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000005018 casein Substances 0.000 description 2
- 235000021240 caseins Nutrition 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000032798 delamination Effects 0.000 description 2
- 235000010985 glycerol esters of wood rosin Nutrition 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- 229920001194 natural rubber Polymers 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- 239000012260 resinous material Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-Dichloroethene Chemical compound ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N 1-ethenoxybutane Chemical compound CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- JGRXEBOFWPLEAV-UHFFFAOYSA-N 2-ethylbutyl prop-2-enoate Chemical compound CCC(CC)COC(=O)C=C JGRXEBOFWPLEAV-UHFFFAOYSA-N 0.000 description 1
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- JHLNERQLKQQLRZ-UHFFFAOYSA-N Calcium silicate Chemical compound [Ca+2].[Ca+2].[O-][Si]([O-])([O-])[O-] JHLNERQLKQQLRZ-UHFFFAOYSA-N 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L Calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- YACLQRRMGMJLJV-UHFFFAOYSA-N Chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 1
- 229920001368 Crepe rubber Polymers 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000000899 Gutta-Percha Substances 0.000 description 1
- 229920000588 Gutta-percha Polymers 0.000 description 1
- 229920000126 Latex Polymers 0.000 description 1
- 240000000342 Palaquium gutta Species 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- WKEDVNSFRWHDNR-UHFFFAOYSA-N Salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 description 1
- HWHLPVGTWGOCJO-UHFFFAOYSA-N Trihexyphenidyl Chemical compound C1CCCCC1C(C=1C=CC=CC=1)(O)CCN1CCCCC1 HWHLPVGTWGOCJO-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- VFGRALUHHHDIQI-UHFFFAOYSA-N butyl 2-hydroxyacetate Chemical compound CCCCOC(=O)CO VFGRALUHHHDIQI-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- 231100000078 corrosive Toxicity 0.000 description 1
- 231100001010 corrosive Toxicity 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 239000011928 denatured alcohol Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 150000002019 disulfides Chemical class 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 238000011068 load Methods 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000003638 reducing agent Substances 0.000 description 1
- 239000012262 resinous product Substances 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N silicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- 239000010875 treated wood Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 230000002087 whitening Effects 0.000 description 1
- 239000001052 yellow pigment Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
- H01B3/447—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from acrylic compounds
-
- 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
- Y10T428/26—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension
- Y10T428/266—Web or sheet containing structurally defined element or component, the element or component having a specified physical dimension of base or substrate
-
- 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
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2843—Web or sheet containing structurally defined element or component and having an adhesive outermost layer including a primer layer
-
- 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
- Y10T428/28—Web or sheet containing structurally defined element or component and having an adhesive outermost layer
- Y10T428/2852—Adhesive compositions
- Y10T428/2857—Adhesive compositions including metal or compound thereof or natural rubber
Definitions
- This invention relates to the insulation and protection of electrical conductors, and to insulating tape employed therein.
- Synthetic polymeric materials have recently replaced rubber and guttapercha to a great extent in the insulation of wires and cables, par-- ticularly those exposed to outdoor conditions or to oils or solvents.
- Materials such as polyvinyl chloride and polymers of ethylene, for example, have been applied by extrusion methods to copper wires to provide insulated conductors having excellent electrical characteristics as well as good chemical and mechanical properties. Such insulated wire has been widely accepted as an improved product.
- the present invention provides, for the first time, means for permanently covering, insulating, and mechanically protecting splices in polymar-covered wires as just described, by simple hand application of a single strip of stable, stretchable, retractable, pressure-sensitive adhesive tape.
- Our novel tape also has many adclitioncl uses, as hereinafter suggested.
- polyvinyl chloride plasticized with not more than parts of the usual plasticizer such as tricresyl phosphate or dioctyl phthalate has been sheeted out in roll form in thicknesses up to 4. mils or greater, and coated with a specific pressure-sensitive adhesive consisting of rubber,-
- Films, or coated adhesive tapes, having these properties cannot readily-be applied by hand to wire splices or the lme. While thinner films of similar composition might conceivably be used because oi their reduced strength per unit of width, the-low elasticity still precludes the acceptance of such tapes for applications such as the covering of wire splices. In addition, thicknesses of at least about four mils, and
- Films have also been prepared with increased amounts of dioctyl phthalate or the like in an attempt to reduce the stress requirements and improve the elasticity.
- a composition consisting of 100 parts of a vinyl chloride polymer and 33 parts of dioctyl phthalate was calendered to a thickness of four mils and coated with a pressure-sensitive adhesive as hereinabcve described. While the physical properties of the film were much improved, it was found that this particular adhesive as wellas various other pres sure-sensitive adhesives rapidly became soft and pasty when in contact with this or other vinyl polymerv films containing more than about 20: ⁇
- the present invention avoids these and other which may be readily and quickly prepared without the use of special procedures or equipment. These unique and valuable results are obtained of stretch in the final film.
- an insulating tape in the form of a relatively thick but easily stretchable and highly elastic pressure-sensitive adhesive tape comprising a well-bonded, water-insoluble, non-corrosive, normally tacky and pressure-sensitive adhesive coating on a plasticized vinyl chloride polymer film which is in permanent equilibrium with the adhesive.
- permanent equilibrium it is meant that the pressure-sensitive adhesive layer neither softens (becomes pasty”) nor loses tackiness (becomes non-adherent on prolonged contact with the backing or film layer.
- the adhesive remains aggressively tacky, and also remains eucohesive (by which it is meant that it is more cohesive than adhesive such that ofisetting or transfer of adhesive material does not result when the tape is unwound from rolls or removed from surfaces to which temporarily applied and can be handled without transfer of adhesive material to the fingers).
- the vinyl chloride polymer in order to secure permanent equilibrium between backing and adhesive, we employ with the vinyl chloride polymer a combination of modifiers including a substantial but minor amount (not to exceed about 20 parts per 100 parts of the vinyl polymer) of a low molecular weight liquid plasticizer such as dioctyl phthalate, together with a substantially equal or somewhat greater amount of a high molecular weight resinous type plasticizer, the amount of the latter in any event being sufficient, together with the liquid plasticizer, to provide the desired degree Paraplex G-" is a preferred example of a suitable resinous type plasticizer.
- a combination of modifiers including a substantial but minor amount (not to exceed about 20 parts per 100 parts of the vinyl polymer) of a low molecular weight liquid plasticizer such as dioctyl phthalate, together with a substantially equal or somewhat greater amount of a high molecular weight resinous type plasticizer, the amount of the latter in any event being sufficient, together with the liquid plasticizer, to provide the desired degree Paraplex G-" is a
- Resinous Products 8 Chemicals Corp., and is a soft, viscous alkyd resin having a specific gravity of 1.06, and an acid number of not more than 2.0; it is soluble in esters, ketones, aromatic and chlorinated hydrocarbons.
- Another high-molecular-weight plasticizer material which has been found useful in providing suitably stretchable and elastic vinyl polymer films is polymerized ethyl acrylate.
- Another example is polymerized vinyl butyl ether.
- resinous or high molecular weight modifiers such as Paraplex G25" are themselves capable of producing the desired degree of strength, stretch and elasticity in vinyl chloride polymer films, and furthermore are generally classed as nommigrating or permanent type modifiers or plasticizers, it is surprisingly found that these materials donot provide for permanent equilibrium of adhesive and backing as herein defined. Instead, it has been shown that pressure-sensitive adhesives in prolonged contact with highly stretchable and elastic films consisting solely of vinyl polymer and resinous modifier lose a great deal, if not all, of their initial tackiness or pressure-sensitivity.
- the present invention provides an electrical insulating tape having properties of stretch and elasticity which render it highly eiiective for wrapping wire and cable splices.
- the tape is stretchable to the extent of at least about 50% at room temperature as measured in a tensile tester (such as a Serigraph Model I-P-4, manufactured by the Henry L. Scott Co. of Buffalo, R. I.)
- the tape can be readily stretched to this extent by pulling between the hands.
- the invention provides tapes which are stretchable to the extent of at least about 100%, which is preferred.
- the elasticity of the tape is a valuable feature'in making possible snug wrappings and coverings.
- the present tape is highly elastic as shown by the fact that when a strip is elongated 30% at room temperature and then released it will retract at room temperature to substantially the original length,
- the invention provides tapes that will substantially completely retract when elongated as much as 50% or even more. Ihe method employed for making such retraction tests of elasticity is as follows. A number of tape lengths are cut. Each length is suspended from an upper clamp and is provided with a light clamp (weighing about 10 grams) at the lower end to provide means for applying a Weight. Each tape strip is 1 inch wide and 5 inches long between clamps. Weights of various amounts are applied to the different samples to determine what weight is needed to produce the desired elongation (30%, for example) in 15 sec onds.
- the weight is promptly removed at the end of the 15 seconds, and the length of the tape between clamps is measured at difierent time intervals to determine the retraction.
- the weight of the lower clamp is relatively so minute that it does not affect the result.
- the preferred thickness of the backing film for the electrical tape is 4 to 20 mils. A thickness of about 5 to 10 mils is generally most useful.
- hesive tape may be used to bind together a number of insulated electrical conductors into a permanently compact, flexible, oil-resistant bundle or harness, by spirally winding such a bundle with a single overlapping strip of the tape applied under considerable tension.
- a similar spiral winding onmetal racks employed in electroplating operations provides a chemically resistant coating which remains firmly attached to the rack during immersion in the plating bath.
- Single thicknesses of the tape are useful as abrasion or wear-resistant adherent surface coatings on flat or curved surfaces.
- insulating tapes in the form of pressure-sensitive adhesive tapes having a vinyl polymer film base were prepared with a vinyl chloride-vinyl acetate copolymer softening at about 280 F. and in which the ratio of vinyl chloride to vinyl acetate was approximately 89:11.
- the commercially available "Vinylite VYNS,” sold by Carbide and Carbon Chemical Corp, is a suitable copolymer corresponding to vinyl acetate monomer ratios, such as :5.
- Polyvinyl chloride itself is satisfactory in many formulations, as are many of the copolymers of vinyl chloride and vinylidene chloride, of which one example is Geon 200-X-6, a vinyl chloridevinylidene chloride copolymer having a softening temperature of about 260 F., sold by B. F. Goodrich Co. Polymers softening at 300 F. or higher are ordinarily to be preferred where extremely high heat resistance solvent resistance, and'the like are essential.
- plasticizers other than the di octyl phthalate of the various examples may be substituted therefor.
- the plasticizer must be compatible with. the vinyl polymer, and must be sufficiently low in volatility so that it is not driven off during milling and caleudering, or during subsequent storage and use. Tricresyl phosphate.
- various compatible non-migrating resinous or high molecular weight modifying materlals having a plasticizing efiect on the vinyl polymer employed may be substituted in whole or in part for the specific alkyd resin hereinbefore mentioned.
- Ethyl acrylate polymer has been found useful, as previously noted; this modifier has somewhat less tendency to cause tack loss than does the Para les 6-25, hence may be used in even greater amounts-in many formulations.
- a resinous material. having properties esscntially equivalent to Paraplex (3-25 for our purposes has been prepared by heating together sebacic acid, propylene glycol, and ethylene glycol in a 102911 molar ratio to a low acid number.
- modifying agents which impart specific properties to the film may be added it desired.
- a small amount of calcium stcarate added prior to milling and calendering acts as a. stabilizer in preventing darkening of the vinyl polymer or of the film.
- Other examples are lead silicate, calcium silicate, and triethanolaminc.
- the tape products herein described are most conveniently and economically prepared by a series of steps including pro-mixing, milling, and calendering the vinyl polymer-plasticizer mixture into continuous film form, temporarily attaching the film to a carrier belt or Web, coating the exposed surface of the film with an adhesive primer and subsequently with a pressuresensitive adhesive, removing the coated film from the carrier, slitting into narrow widths, and winding the resultingadhesive tape into roll form on suitable cores.
- calendaring other means may be employed for forming the film. Deposition from solution in a suitable volatile liquid vehicle, followed by heating to remove the vehicle and, where necessary, to homogenize the film, has some advantages, particularly in the case of the thinner films. However, the action of the calender or similar devices seems to impart. some additional and desirable properties to the resulting film, particularly with respect to stretchiness and elasticity, and such methods are generally to be preferred.
- a varnished cambric or Holland cloth carrier belt is used, sufficient adhesion of film to belt may be obtained simply by combining the two on the bottom roll of the calender under a light pressure and with the roll at a temperature of the order of lid" 1 a heavy paper web with a light weight surface coating; of a low tack pressure-sensitive adhesive may economically replace the varnished cambrlc.
- the carrier web is simply an aid to the successful commercial coating of the highly stretchable film, and may be dispensed with where other suitable methods of handling this type of material are available.
- Primer and adhesive compositions are preferably, but not necessarily, applied from solution or suspension in a volatile liquid vehicle, as
- the volatile vehicle is removed after each coating operation, preferably by evaporation at elevated temperatures.
- a mixture of 700 parts by weight of Vinylite VYNS, 200 parts of Paraplex CT-25, 100 parts of dioctyl phthalate and 25 parts calcium stearate was milled together on a rubber mill, previously heated to 250 until homogeneous, and was then calendered to a thickness of a mils.
- the resulting transparent him was lightly bonded to a varnished cambric carrier web, and was then primed, after which it was coated with a pressure sensitive adhesive.
- the primer was made by mixing 985 lbs. of an animoniacal casein solution containing lbs. oi casein with 624 lbs.
- the heptane was then added in small portions, and sufizlcient alcohol was finally added to bring the viscosity to the proper value for coating.
- the primed film was coated with the adhesive solution, followed by drying to remove the solvent. About 6.5 to 7.5 grains of adhesive, on the dry basis. were applied to 24 square inches of the film.
- the coated film was removed from the temporary liner and slit into narrow widths.
- the resulting tape was highly stretchable and elastic, and provided an excellent insulating and protectlng covering when wound around an electrical conductor. On an irregular surface, such as a wire splice, the elasticity or regain was sufficient to provide an extremely compact covering.
- the tape was found to have at least about stretch, and a tensile strength of about 20 lbs. per inch width.
- Strips of the tape were stretched to 20% and to 50% elongation, and were then allowed to reof the pressure-sensitive adhesive coating re mained unchanged.
- films prepared from the above ingredients in the proportions 109:2?52612, primed, and coated with adhesive were found to be too tough and inelastic for most uses, even though the adhesive coating remained tacky and in good condition.
- films were elongated to more than approximately ten or twenty per cent of their initial length, they were found to acquire a permanent set and would not then retract to their origin g length.
- adhesivescoated on films plasticized with from 40 to 70 parts of Paraplex (Ii-25 and in the absence of the dioctyl phthalate were soon found to become deficient in tackiness.
- Example 2 The plasticized vinyl polymer film of Example 1 was primed with a synthetic rubber-resin primer composition applieoi irom solution in organic solvent, and coated with a natural rubber base pressure-sensitive adhesive.
- the resulting transparent pressure-sensitive adhesive tape was useful for wrapping splices in electrical conductors and for other purposes. The adhesive and backing were found to be in permanent equilibrium. The transparent nature of the tape was advantageous where it was desirable periodically to inspect the protected surface.
- composition used as the primer in this example consisted of a solution, in a mixture of 100 parts toluol and parts methyl ethyl ketone, of 20 parts of a pure hydrocarbon thermoplastic terpene resin having a melting point of 115 F. and a zero acid number, and parts of a rubbery butadiene-acrylonitrile copolymer.
- the transparent pressure-sensitive adhesive was prepared by blending 288 lbs. of latex crepe rubber, 175 lbs. of the thermoplastic terpene resin having a melting point of 115 F, 2.88 lbs. of tetramethyl thiupam disulfide, and 3 lbs. of an antioxidant such as Flectol H (a condensation product of acetone and aniline melting at 120 (3.), in solution in heptane containing a small amount or denatured alcohol as a viscosity reducing agent.
- Flectol H a condensation product of acetone and aniline melting at 120 (3.
- Example 3 I Various pigments and colors may be added both to the backing and to the adhesive formulation of my insulating composition in order to improve the appearance, or to provide a distinctive color, or for other purposes. Heavy pigment loading of the vinyl film for example is found to improve the heat resistance.
- a film twelve mils in thickness was prepared from a mixture of mo parts Vinylite VYNS, 200 parts Parapler; G-ZE, lilo parts dioctyl phthalate, liilll parts titanium dioxide pigment, and parts calcium steal-ate, together with 100 parts of a mold inhibiting agent such as Shirlan Extra (sallcyl anilide).
- the film was primed with the primer of Example 2 and coated with a polyacrylate base pressure-sensitive adhesive.
- the adhesive was composed of a eopoly'mer of 75 parts or 2ethylbutyl acrylate and 25 parts ethyl acrylate, tackiz'ied with a thermoplastic terpene resin, and firmed up by heating with small admixed amounts of zinc resina'te and an oil soluble heat-reactive phenol-formaldehyde resin. Titanium dioxide was included as a pigment to produce a white adhesive. The produce was cut into narrow widths and wound into roll form, in this case with a varnished cambric interliner.
- Samples of the tape showed approximately l0ll% strength at brealr, and had a tensile strength at break of approximately 30 lbs. per inch width. Retraction to original length from 20% elongation was complete in somewhat under five minutes, and from 50% elongation in ap proximately twenty-four hours.
- Example 3 To produce a completely flame-resistant tape product, the primed film of Example 3 was coated with a pressure-sensitive adhesive consisting essentially of polymerized chloroprene and chlorinated diphenyl in approximately equal proper tions by weight. The adhesive was applied from solution in a high aromatic content hydrocarbon solvent.
- Example 5 To the film composition of Example 1 was added five parts of carbon blaclr. The resulting film had a black glossy appearance and considerably increased tensile strength. The elasticity was somewhat reduced, but the film retracted to its original dimension from approximately 50% elongation in somewhat less than twenty-four hours.
- the film was primed with the primer of Example 2 and coated with an adhesive consisting of parts of a mixture of equal parts of natural rubber and Euna-S synthetic rubber, 50 parts of zinc oxide, 5 parts of carbon black, and 50 parts of heat treated wood rosin. A small amount of Flectol H antioxidant was also added, and the material was dispersed in heptane to a coatable viscosity.
- the resulting tape product was particularly applicable to the covering of splices in copper wires carrying an insulating coating of black pigmented plasticized synthetic polymer.
- No pressure-sensitive adhesive tape was previously available which was of sumeases substantially non volatile plasticieing material therefor in an amount within the range of at least about the weight of said polymer but a substantially lesser amount than said polymer and comprising least a major proportion of anon-migrating viscous plasticieer, and the proportions being such that the adhesive tape has the properties of stretch, elasticity and retracta bility hereafter specified without causing pasti ness or loss of the tack of the contacting adhesive; and a water-insoluble normally tacky and pressure-sensitive rubber-resin type adhesive coating united and firmly bonded to one face of said film backing; said film backing being in per manent equilibrium with said pressure sensitive adhesive coating, so as to avoid pastiness or loss of the tack of said adhesive coating and loss of the flexibility of said film backing; said adhesive tape being capable of being wound upon itself in roll form and unwound therefrom without delarnination of the tape or oflsetting of the adhesive, being originally stretchable in widths not greater than about one inch by simple hand pull
- a pressure-sensitive adhesive tape capable of being wound upon itself in roll form and unwound therefrom without delamination or of)- setting of the adhesive and comprising a waterinsol'uble and hydrOcarbthn-oil-insoluble film backing having a thickness of about 4 to mils and formed of a homogeneous miature primarily consisting of a stable blend of (a) a film-forming polymer of monomer material including at least a major proportion of vinyl chloride, and (b) a substantially non-volatile plasticieing material therefor in an amount within the range of at least about the weight of said polymer but not greatly in excess of the weight of said polymer and comprising at least a major proportion of a non-migrating viscous plasticieer resin, and the proportions of the said plasticieing material to said film-forming polymer being such that the adhesive tape has the properties of stretch, elasticity and retractability hereafter specified without causing pastiness or loss of the tack of the contacting adhesive; and a water-
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Adhesive Tapes (AREA)
- Insulating Bodies (AREA)
Description
casts msom'rmc "rare Ralph (lace, New Canada Township, Ramsey County, Robert Burns Snell, Birchwood, and Esther E. Le Page, West Lakcland Township, Washington County, Minn, to Ellinnesota Mining & ll-(Ianufaeturing Gompany, St. Paul, Minn, a corporation of Delaware No Drawing.
Griginal No. 2,559,990, dated any 10, 1951, Serial No. 641,000, January 12, 19%. Application for reissue July 9, 1952, Serial No.
9 Claims.
Matter enclosedin heavy brackets I appears in the original patent but forms no part of this (Cl. sea-s) reissue specification; matter printed in italics indi ates the additions inade'by reissue.
This invention relates to the insulation and protection of electrical conductors, and to insulating tape employed therein.
Synthetic polymeric materials have recently replaced rubber and guttapercha to a great extent in the insulation of wires and cables, par-- ticularly those exposed to outdoor conditions or to oils or solvents. Materials such as polyvinyl chloride and polymers of ethylene, for example, have been applied by extrusion methods to copper wires to provide insulated conductors having excellent electrical characteristics as well as good chemical and mechanical properties. Such insulated wire has been widely accepted as an improved product.
The advantages of such insulation are not fully realized, however, when splices'between lengths of the wire must be covered with previously 'known classes of insulation. The commonly used been used. In such an application, heating and molding are necessary in order to weld the polymer together into an integral insulating layer. The process is inconvenient and time-consuming, and requires special apparatus.
The present invention provides, for the first time, means for permanently covering, insulating, and mechanically protecting splices in polymar-covered wires as just described, by simple hand application of a single strip of stable, stretchable, retractable, pressure-sensitive adhesive tape. Our novel tape also has many adclitioncl uses, as hereinafter suggested.
Attempts have previously been made to provide similar strips, or films, of polymer with adhesive coatings so as to avoid the necessity of the subsequent heating and molding operations in covering and insulating wire splices. For example, polyvinyl chloride plasticized with not more than parts of the usual plasticizer such as tricresyl phosphate or dioctyl phthalate has been sheeted out in roll form in thicknesses up to 4. mils or greater, and coated with a specific pressure-sensitive adhesive consisting of rubber,-
polyisobutylene, and a resinous material, in an attempt to produce a transparent flexible ad- 2: hesive tape or sheet. With. this amount of plasticizer, however, the sheet is found to be quite stiff and rigid. Very high stress is required to obtain any appreciable elongation; for example, a strip one inch in width and .004 inch in thickness of a mixture of 100 parts of an 89:11 vinyl chloride-vinyl acetate copolymer and 20 parts of dioctyl phthalate required a stress of 30 lbs. to produce even as little as 10% elongation. Increased elongation results in a whitening of the film, and the stretched film will then no longer retract to its original length at room temperature. Films, or coated adhesive tapes, having these properties cannot readily-be applied by hand to wire splices or the lme. While thinner films of similar composition might conceivably be used because oi their reduced strength per unit of width, the-low elasticity still precludes the acceptance of such tapes for applications such as the covering of wire splices. In addition, thicknesses of at least about four mils, and
even up to twelve mils or somewhat higher, are.
generally preferred by electricians because of the reduced number of turns required for adequate insulation, as well as the absence-of the fiimsiness characteristic of thinner films.
Films have also been prepared with increased amounts of dioctyl phthalate or the like in an attempt to reduce the stress requirements and improve the elasticity. Thus, a composition consisting of 100 parts of a vinyl chloride polymer and 33 parts of dioctyl phthalate was calendered to a thickness of four mils and coated with a pressure-sensitive adhesive as hereinabcve described. While the physical properties of the film were much improved, it was found that this particular adhesive as wellas various other pres sure-sensitive adhesives rapidly became soft and pasty when in contact with this or other vinyl polymerv films containing more than about 20:}
The resultin parts of liquid type plasticizers; tape, when wound under tension around 2. splice or bundle of wires, soon loosened and became ineffective. This tendency was increased with even slight increase in temperature above normal room temperature.
The present invention avoids these and other which may be readily and quickly prepared without the use of special procedures or equipment. These unique and valuable results are obtained of stretch in the final film.
eases U\ t by utilizing an insulating tape in the form of a relatively thick but easily stretchable and highly elastic pressure-sensitive adhesive tape comprising a well-bonded, water-insoluble, non-corrosive, normally tacky and pressure-sensitive adhesive coating on a plasticized vinyl chloride polymer film which is in permanent equilibrium with the adhesive. By permanent equilibrium it is meant that the pressure-sensitive adhesive layer neither softens (becomes pasty") nor loses tackiness (becomes non-adherent on prolonged contact with the backing or film layer. The adhesive remains aggressively tacky, and also remains eucohesive (by which it is meant that it is more cohesive than adhesive such that ofisetting or transfer of adhesive material does not result when the tape is unwound from rolls or removed from surfaces to which temporarily applied and can be handled without transfer of adhesive material to the fingers).
In order to secure permanent equilibrium between backing and adhesive, we employ with the vinyl chloride polymer a combination of modifiers including a substantial but minor amount (not to exceed about 20 parts per 100 parts of the vinyl polymer) of a low molecular weight liquid plasticizer such as dioctyl phthalate, together with a substantially equal or somewhat greater amount of a high molecular weight resinous type plasticizer, the amount of the latter in any event being sufficient, together with the liquid plasticizer, to provide the desired degree Paraplex G-" is a preferred example of a suitable resinous type plasticizer. It is sold .by Resinous Products 8: Chemicals Corp., and is a soft, viscous alkyd resin having a specific gravity of 1.06, and an acid number of not more than 2.0; it is soluble in esters, ketones, aromatic and chlorinated hydrocarbons. Another high-molecular-weight plasticizer material which has been found useful in providing suitably stretchable and elastic vinyl polymer films is polymerized ethyl acrylate. Another example is polymerized vinyl butyl ether.
While resinous or high molecular weight modifiers such as Paraplex G25" are themselves capable of producing the desired degree of strength, stretch and elasticity in vinyl chloride polymer films, and furthermore are generally classed as nommigrating or permanent type modifiers or plasticizers, it is surprisingly found that these materials donot provide for permanent equilibrium of adhesive and backing as herein defined. Instead, it has been shown that pressure-sensitive adhesives in prolonged contact with highly stretchable and elastic films consisting solely of vinyl polymer and resinous modifier lose a great deal, if not all, of their initial tackiness or pressure-sensitivity. When tape made in this Way is unwound from roll form, after a moderate period of storage, and applied to a splice, it does not adhere either to the electrical conductor or to its own backing, and hence is of no value as an insulating and protective coating.
The present invention provides an electrical insulating tape having properties of stretch and elasticity which render it highly eiiective for wrapping wire and cable splices. The tape is stretchable to the extent of at least about 50% at room temperature as measured in a tensile tester (such as a Serigraph Model I-P-4, manufactured by the Henry L. Scott Co. of Providence, R. I.) The tape can be readily stretched to this extent by pulling between the hands. In fact, the invention provides tapes which are stretchable to the extent of at least about 100%, which is preferred. The elasticity of the tape is a valuable feature'in making possible snug wrappings and coverings. The present tape is highly elastic as shown by the fact that when a strip is elongated 30% at room temperature and then released it will retract at room temperature to substantially the original length, The invention provides tapes that will substantially completely retract when elongated as much as 50% or even more. Ihe method employed for making such retraction tests of elasticity is as follows. A number of tape lengths are cut. Each length is suspended from an upper clamp and is provided with a light clamp (weighing about 10 grams) at the lower end to provide means for applying a Weight. Each tape strip is 1 inch wide and 5 inches long between clamps. Weights of various amounts are applied to the different samples to determine what weight is needed to produce the desired elongation (30%, for example) in 15 sec onds. In the case of this sample, the weight is promptly removed at the end of the 15 seconds, and the length of the tape between clamps is measured at difierent time intervals to determine the retraction. The weight of the lower clamp is relatively so minute that it does not affect the result.
The preferred thickness of the backing film for the electrical tape is 4 to 20 mils. A thickness of about 5 to 10 mils is generally most useful.
' hesive tape may be used to bind together a number of insulated electrical conductors into a permanently compact, flexible, oil-resistant bundle or harness, by spirally winding such a bundle with a single overlapping strip of the tape applied under considerable tension. A similar spiral winding onmetal racks employed in electroplating operations provides a chemically resistant coating which remains firmly attached to the rack during immersion in the plating bath. Single thicknesses of the tape are useful as abrasion or wear-resistant adherent surface coatings on flat or curved surfaces.
The following examples of insulating tapes in the form of pressure-sensitive adhesive tapes having a vinyl polymer film base were prepared with a vinyl chloride-vinyl acetate copolymer softening at about 280 F. and in which the ratio of vinyl chloride to vinyl acetate was approximately 89:11. The commercially available "Vinylite VYNS," sold by Carbide and Carbon Chemical Corp, is a suitable copolymer corresponding to vinyl acetate monomer ratios, such as :5. Polyvinyl chloride itself is satisfactory in many formulations, as are many of the copolymers of vinyl chloride and vinylidene chloride, of which one example is Geon 200-X-6, a vinyl chloridevinylidene chloride copolymer having a softening temperature of about 260 F., sold by B. F. Goodrich Co. Polymers softening at 300 F. or higher are ordinarily to be preferred where extremely high heat resistance solvent resistance, and'the like are essential.
Many liquid plasticizers other than the di octyl phthalate of the various examples may be substituted therefor. The plasticizer must be compatible with. the vinyl polymer, and must be sufficiently low in volatility so that it is not driven off during milling and caleudering, or during subsequent storage and use. Tricresyl phosphate.
'dibutyl phthalates, and butyl phthalyl butyl glycollate, for example, appear to be equally effective in most of the compositions herein described. All of these compounds are capable of producing pastiness in water-insoluble pressure-sensitive adhesives coated on vinyl bookings when used in proportions greater than about 29 parts per 100 parts of the vinyl polymer.
Likewise, various compatible non-migrating resinous or high molecular weight modifying materlals having a plasticizing efiect on the vinyl polymer employed may be substituted in whole or in part for the specific alkyd resin hereinbefore mentioned. Ethyl acrylate polymer has been found useful, as previously noted; this modifier has somewhat less tendency to cause tack loss than does the Para les 6-25, hence may be used in even greater amounts-in many formulations. A resinous material. having properties esscntially equivalent to Paraplex (3-25 for our purposes has been prepared by heating together sebacic acid, propylene glycol, and ethylene glycol in a 102911 molar ratio to a low acid number.
It will be understood that, where specific ratios of specific polymers, low molecular weight plasticizers, and high molecular weight plasticizers are described in the examples, substitution of equivalent but somewhat different materials may require alteration of these ratios in order to obtain equivalent results, all in conformity with Well-recognized principles.
Various modifying agents which impart specific properties to the film may be added it desired. For example, a small amount of calcium stcarate added prior to milling and calendering acts as a. stabilizer in preventing darkening of the vinyl polymer or of the film. Other examples are lead silicate, calcium silicate, and triethanolaminc.
In general, the tape products herein described are most conveniently and economically prepared by a series of steps including pro-mixing, milling, and calendering the vinyl polymer-plasticizer mixture into continuous film form, temporarily attaching the film to a carrier belt or Web, coating the exposed surface of the film with an adhesive primer and subsequently with a pressuresensitive adhesive, removing the coated film from the carrier, slitting into narrow widths, and winding the resultingadhesive tape into roll form on suitable cores. In place of calendaring, other means may be employed for forming the film. Deposition from solution in a suitable volatile liquid vehicle, followed by heating to remove the vehicle and, where necessary, to homogenize the film, has some advantages, particularly in the case of the thinner films. However, the action of the calender or similar devices seems to impart. some additional and desirable properties to the resulting film, particularly with respect to stretchiness and elasticity, and such methods are generally to be preferred.
Where a varnished cambric or Holland cloth carrier belt is used, sufficient adhesion of film to belt may be obtained simply by combining the two on the bottom roll of the calender under a light pressure and with the roll at a temperature of the order of lid" 1 a heavy paper web with a light weight surface coating; of a low tack pressure-sensitive adhesive may economically replace the varnished cambrlc. In any event, the carrier web is simply an aid to the successful commercial coating of the highly stretchable film, and may be dispensed with where other suitable methods of handling this type of material are available.
Primer and adhesive compositions are preferably, but not necessarily, applied from solution or suspension in a volatile liquid vehicle, as
shown in the examples. The volatile vehicle is removed after each coating operation, preferably by evaporation at elevated temperatures.
Example i.
A mixture of 700 parts by weight of Vinylite VYNS, 200 parts of Paraplex CT-25, 100 parts of dioctyl phthalate and 25 parts calcium stearate was milled together on a rubber mill, previously heated to 250 until homogeneous, and was then calendered to a thickness of a mils. The resulting transparent him was lightly bonded to a varnished cambric carrier web, and was then primed, after which it was coated with a pressure sensitive adhesive. The primer was made by mixing 985 lbs. of an animoniacal casein solution containing lbs. oi casein with 624 lbs. of an aqueous dispersion containing 38% by weight of a coplymer of 50 parts butadiene and 50 parts styrene. The primer coating was dried to remove the water, resulting in an extremely thin primer film. The formula of the pressure-sensitive adhesivc was as follows:
Parts by weight Robbery butadlene-styrene copolymer 10o Zinc oxide 5 Titanium dioxide 10 Yellow pigment 0.3 Oil-soluble heat-reactive phenol-aldehyde resin l2 Ester gum l. 40 Paraffin oil 25 Soft cournarone-indene resin 40 Heptane 30D Alcohol "About 10 In compounding the adhesive, the copclymer and pigments were first milled together. The will base was then blended with the ester gum, paraffin. oil, coumarone-idene resin, and finally with the phenol-aldehyde resin in a heated heavy duty internal mixer. After a brief further heating at a higher temperature; the batch was cooled. The heptane was then added in small portions, and sufizlcient alcohol was finally added to bring the viscosity to the proper value for coating. The primed film was coated with the adhesive solution, followed by drying to remove the solvent. About 6.5 to 7.5 grains of adhesive, on the dry basis. were applied to 24 square inches of the film.
The coated film was removed from the temporary liner and slit into narrow widths. The resulting tape was highly stretchable and elastic, and provided an excellent insulating and protectlng covering when wound around an electrical conductor. On an irregular surface, such as a wire splice, the elasticity or regain was sufficient to provide an extremely compact covering. The tape was found to have at least about stretch, and a tensile strength of about 20 lbs. per inch width.
Strips of the tape were stretched to 20% and to 50% elongation, and were then allowed to reof the pressure-sensitive adhesive coating re mained unchanged.
Increasing the plasticizers in the above film to a final formula of 100:30220 yielded a composition which, in the form of 4 mil film, was found to be somewhat weak. However, this composition produced a reasonably satisfactory backing in thicknesses of about twelve mils. Pressuresensitive adhesives coated on this backing were found to soften to a very slight extent after prolonged ageing in the final tape rolls, but the tape.
remained fully satisfactory for such uses as the binding of harnesses and the lilre.
On the other hand, films prepared from the above ingredients in the proportions 109:2?52612, primed, and coated with adhesive, were found to be too tough and inelastic for most uses, even though the adhesive coating remained tacky and in good condition. When such films were elongated to more than approximately ten or twenty per cent of their initial length, they were found to acquire a permanent set and would not then retract to their origin g length. A slight increase in the proportion of dioctyl phthalate, for example, to about eight or ten parts, improved the films in this respect. On the other hand, adhesivescoated on films plasticized with from 40 to 70 parts of Paraplex (Ii-25 and in the absence of the dioctyl phthalate were soon found to become deficient in tackiness.
Example 2 The plasticized vinyl polymer film of Example 1 was primed with a synthetic rubber-resin primer composition applieoi irom solution in organic solvent, and coated with a natural rubber base pressure-sensitive adhesive. The resulting transparent pressure-sensitive adhesive tape was useful for wrapping splices in electrical conductors and for other purposes. The adhesive and backing were found to be in permanent equilibrium. The transparent nature of the tape was advantageous where it was desirable periodically to inspect the protected surface.
The composition used as the primer in this example consisted of a solution, in a mixture of 100 parts toluol and parts methyl ethyl ketone, of 20 parts of a pure hydrocarbon thermoplastic terpene resin having a melting point of 115 F. and a zero acid number, and parts of a rubbery butadiene-acrylonitrile copolymer.
The transparent pressure-sensitive adhesive was prepared by blending 288 lbs. of latex crepe rubber, 175 lbs. of the thermoplastic terpene resin having a melting point of 115 F, 2.88 lbs. of tetramethyl thiupam disulfide, and 3 lbs. of an antioxidant such as Flectol H (a condensation product of acetone and aniline melting at 120 (3.), in solution in heptane containing a small amount or denatured alcohol as a viscosity reducing agent.
I Example 3 I Various pigments and colors may be added both to the backing and to the adhesive formulation of my insulating composition in order to improve the appearance, or to provide a distinctive color, or for other purposes. Heavy pigment loading of the vinyl film for example is found to improve the heat resistance.
A film twelve mils in thickness was prepared from a mixture of mo parts Vinylite VYNS, 200 parts Parapler; G-ZE, lilo parts dioctyl phthalate, liilll parts titanium dioxide pigment, and parts calcium steal-ate, together with 100 parts of a mold inhibiting agent such as Shirlan Extra (sallcyl anilide). The film was primed with the primer of Example 2 and coated with a polyacrylate base pressure-sensitive adhesive. The adhesive was composed of a eopoly'mer of 75 parts or 2ethylbutyl acrylate and 25 parts ethyl acrylate, tackiz'ied with a thermoplastic terpene resin, and firmed up by heating with small admixed amounts of zinc resina'te and an oil soluble heat-reactive phenol-formaldehyde resin. Titanium dioxide was included as a pigment to produce a white adhesive. The produce was cut into narrow widths and wound into roll form, in this case with a varnished cambric interliner.
Samples of the tape showed approximately l0ll% strength at brealr, and had a tensile strength at break of approximately 30 lbs. per inch width. Retraction to original length from 20% elongation was complete in somewhat under five minutes, and from 50% elongation in ap proximately twenty-four hours.
Example To produce a completely flame-resistant tape product, the primed film of Example 3 was coated with a pressure-sensitive adhesive consisting essentially of polymerized chloroprene and chlorinated diphenyl in approximately equal proper tions by weight. The adhesive was applied from solution in a high aromatic content hydrocarbon solvent.
Example 5 To the film composition of Example 1 was added five parts of carbon blaclr. The resulting film had a black glossy appearance and considerably increased tensile strength. The elasticity was somewhat reduced, but the film retracted to its original dimension from approximately 50% elongation in somewhat less than twenty-four hours.
The film was primed with the primer of Example 2 and coated with an adhesive consisting of parts of a mixture of equal parts of natural rubber and Euna-S synthetic rubber, 50 parts of zinc oxide, 5 parts of carbon black, and 50 parts of heat treated wood rosin. A small amount of Flectol H antioxidant was also added, and the material was dispersed in heptane to a coatable viscosity. The resulting tape product was particularly applicable to the covering of splices in copper wires carrying an insulating coating of black pigmented plasticized synthetic polymer.
It will be seen that herez'uaboue we have described various embodiments of our invention for purposes of illustration. The novel article of our invention is a broadly new article of commerce. Prior to our invention there was no electrical or plastic tape available which was similar to the product of this invention either in performance characteristics or in appearance or handling characteristics. No pressure-sensitive adhesive tape was previously available which was of sumeases substantially non volatile plasticieing material therefor in an amount within the range of at least about the weight of said polymer but a substantially lesser amount than said polymer and comprising least a major proportion of anon-migrating viscous plasticieer, and the proportions being such that the adhesive tape has the properties of stretch, elasticity and retracta bility hereafter specified without causing pasti ness or loss of the tack of the contacting adhesive; and a water-insoluble normally tacky and pressure-sensitive rubber-resin type adhesive coating united and firmly bonded to one face of said film backing; said film backing being in per manent equilibrium with said pressure sensitive adhesive coating, so as to avoid pastiness or loss of the tack of said adhesive coating and loss of the flexibility of said film backing; said adhesive tape being capable of being wound upon itself in roll form and unwound therefrom without delarnination of the tape or oflsetting of the adhesive, being originally stretchable in widths not greater than about one inch by simple hand pull-- ing, exercising a force of not more than about to pounds, to an extent of at least 50% at room temperature and being substantially completely retractable from an elongation of 30%, as herein specified; said tape being readily con formable to irregular surfaces and its elasticity, retractability and highadhesion value making it easy to produce snug, smooth-fitting wrappings and coverings. 1
8. A pressure-sensitive adhesive tape capable of being wound upon itself in roll form and unwound therefrom without delamination or of)- setting of the adhesive and comprising a waterinsol'uble and hydrOcarbthn-oil-insoluble film backing having a thickness of about 4 to mils and formed of a homogeneous miature primarily consisting of a stable blend of (a) a film-forming polymer of monomer material including at least a major proportion of vinyl chloride, and (b) a substantially non-volatile plasticieing material therefor in an amount within the range of at least about the weight of said polymer but not greatly in excess of the weight of said polymer and comprising at least a major proportion of a non-migrating viscous plasticieer resin, and the proportions of the said plasticieing material to said film-forming polymer being such that the adhesive tape has the properties of stretch, elasticity and retractability hereafter specified without causing pastiness or loss of the tack of the contacting adhesive; and a water-insoluble, normally tacky and pressure-sensitive rubber resin type adhesive coating united and firmly bonded to one face of said film backing, said adhesive coating being thin in relation to said 'fiim backing; said film backing being in permanent equilibrium with said pressnre-sensitive adhesive coating, so as to avoid pastiness or loss of the tack of said adhesive coating and loss of the flexibility of said film backing; said adhesive tape being capable of being wound upon itself in roll form and unwound therefrom without delamination of the tape or offsetting of the adhesive, being originally stretchable in widths. not greater than about one inch by simple hand pulling, exercising a force of not more than about 10 to 15 pounds, to an extent of at least 50% at room temperature and being substantially completely retractable from an elongation of as herein specified; said tape being readily conformable to irregular surfaces and its elastic-iii retractability and high adhesion value making it easy to produce snug, smooth fitting israppings and covertags.
9. A pressure-sensitive adhesive insulating tape wound upon itself in roll form and comprising: (1) a wateninsoluble hydrocarbon oil-insoluble opaque pigmented film batching of high dielectric strength and having a thickness of about 4 to 12 mils and formed of a homogeneous mix-- ture primarily consisting of a stable blend of (a) a film forming polymer of monomers including at least a major proportion of vinyl chloride, and (b) a substantially non-volatile plasticieing material therefor in an amount within the range of at least about V the weight of said polymer but not in excess of about V2 the weight of said polymer and comprising least a major proportion of a non-migrating viscous plasticizer resin, and the proportions of said plasticizing material to saw film-forming polymer being such that the adhesive tape has the properties of stretch, elasticity and retractability hereafter specified without causing nastiness or loss of the tack of the contacting adhesive in the roll; (2) an adhesive primer coating on said film backing so as to increase the anchorage of the adhesive coating to the inner face o its bashing when unwound from rolls thereof; and (3) a water-insoluble normally tacky and pressure-sensitive rubber resin type adhesive coating united to the inner face of said film backing, adhesive coating being thin in relation to said film backing; said film backing being in permanent equilibrium with said pressure-sensitive adhesive coating so as to avoid nastiness or loss of the inch of the said adhesive coating and diminution of the flexibility of said film backing; said adhesive tape being unwindable from the roll without deiamination of the tape or offsetting of the adhesive, being originally stretchable in widths not greater than about one inch by simple hand pulling, exercising a force or more than about ill to 15 pounds, to an ea:- tent of at least at room temperature and being substantially completely retractable from an elongation of 33%, as herein specified; said tape being readily conformable to irregular surfaces in insulating wire splices and its elasticity, retractability and high adhesion value making it easy, in insulated splices, to produce snug wrappings and coverings, and said tape having sufficiently aggressive aolhesiveness to remain tightly and snugly wrapped around splices and wires.
References (iii-oil in the file of this patent or the original gatent 'UNETEU PATENTS Number Name Date 1,929,453 Sermon Oct. 10, 1933 1,966,856 staff July 1'7, 1934 2,010,963 Robertson Aug. 13, 1935 2,059,055 Studs Oct. 27, 1936 2,1?0,949 Morgan Aug. 29, 1939 2,312,925 D/lcEmrney et a1 Mar. 2, 1943 2,322,903 Wilkofl June 29, 1943 2,332,265 Schmidt Oct. 1.9, 1943 2,349,413 siem eri May 23, 1944 2,385,319 Eustis Sept. 18, 1945 2,395,419 Mitchell Feb. 26, 1946 2,429,223 Eussls ei; a1 Got. 21, 1947 2,451,132; Taft Oct. 12, 1948 2,462,971 Kitchin ct ell. .Mar. 1, 1949 $610,910 1952 Thomson Sept. 16,
Publications (1)
Publication Number | Publication Date |
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USRE23843E true USRE23843E (en) | 1954-06-29 |
Family
ID=2091483
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US23843D Expired USRE23843E (en) | Insulating tape |
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US (1) | USRE23843E (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2877141A (en) * | 1955-10-27 | 1959-03-10 | Johnson & Johnson | Adhesive coated plastic material |
US2956904A (en) * | 1954-11-04 | 1960-10-18 | Minnesota Mining & Mfg | Pressure-sensitive adhesive tapes |
US3002945A (en) * | 1957-06-10 | 1961-10-03 | Rolle Edward | Thermosetting composition of unsaturated polyester resin and polythio mercaptan |
US3033724A (en) * | 1956-03-26 | 1962-05-08 | Plicoflex Inc | Laminated protective sheath in sheet form and method of applying same to a pipe |
US3073611A (en) * | 1958-11-19 | 1963-01-15 | Hydraulik Gmbh | Means for elongating workpieces |
US3129816A (en) * | 1963-10-31 | 1964-04-21 | Minnesota Mining & Mfg | Pressure-sensitive adhesive tape with plasticized polyvinyl chloride backing |
US3232785A (en) * | 1962-07-06 | 1966-02-01 | Minnesota Mining & Mfg | Pressure-sensitive adhesive sheet |
US6844391B1 (en) | 1998-09-23 | 2005-01-18 | Avery Dennison Corporation | Adhesives with improved rivet properties and laminates using the same |
US9085121B2 (en) | 1999-05-13 | 2015-07-21 | 3M Innovative Properties Company | Adhesive-backed articles |
-
0
- US US23843D patent/USRE23843E/en not_active Expired
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2956904A (en) * | 1954-11-04 | 1960-10-18 | Minnesota Mining & Mfg | Pressure-sensitive adhesive tapes |
US2877141A (en) * | 1955-10-27 | 1959-03-10 | Johnson & Johnson | Adhesive coated plastic material |
US3033724A (en) * | 1956-03-26 | 1962-05-08 | Plicoflex Inc | Laminated protective sheath in sheet form and method of applying same to a pipe |
US3002945A (en) * | 1957-06-10 | 1961-10-03 | Rolle Edward | Thermosetting composition of unsaturated polyester resin and polythio mercaptan |
US3073611A (en) * | 1958-11-19 | 1963-01-15 | Hydraulik Gmbh | Means for elongating workpieces |
US3232785A (en) * | 1962-07-06 | 1966-02-01 | Minnesota Mining & Mfg | Pressure-sensitive adhesive sheet |
US3129816A (en) * | 1963-10-31 | 1964-04-21 | Minnesota Mining & Mfg | Pressure-sensitive adhesive tape with plasticized polyvinyl chloride backing |
US6844391B1 (en) | 1998-09-23 | 2005-01-18 | Avery Dennison Corporation | Adhesives with improved rivet properties and laminates using the same |
US9085121B2 (en) | 1999-05-13 | 2015-07-21 | 3M Innovative Properties Company | Adhesive-backed articles |
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