GB1579433A - Method of applying a plastics to a vulcanized rubber - Google Patents
Method of applying a plastics to a vulcanized rubber Download PDFInfo
- Publication number
- GB1579433A GB1579433A GB14208/76A GB1420876A GB1579433A GB 1579433 A GB1579433 A GB 1579433A GB 14208/76 A GB14208/76 A GB 14208/76A GB 1420876 A GB1420876 A GB 1420876A GB 1579433 A GB1579433 A GB 1579433A
- Authority
- GB
- United Kingdom
- Prior art keywords
- rubber
- plastics
- ethylene
- poly
- sole
- 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
- 238000000034 method Methods 0.000 title claims description 50
- 229920003023 plastic Polymers 0.000 title claims description 49
- 239000004033 plastic Substances 0.000 title claims description 49
- 239000004636 vulcanized rubber Substances 0.000 title claims description 13
- 229920001971 elastomer Polymers 0.000 claims description 63
- 239000005060 rubber Substances 0.000 claims description 63
- -1 poly(vinyl chloride) Polymers 0.000 claims description 45
- 229920002857 polybutadiene Polymers 0.000 claims description 24
- 229920000459 Nitrile rubber Polymers 0.000 claims description 19
- 239000005062 Polybutadiene Substances 0.000 claims description 18
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 16
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- 239000004800 polyvinyl chloride Substances 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 14
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 13
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 12
- 239000005977 Ethylene Substances 0.000 claims description 12
- 229920001577 copolymer Polymers 0.000 claims description 12
- 229920001084 poly(chloroprene) Polymers 0.000 claims description 12
- 229920000728 polyester Polymers 0.000 claims description 11
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 9
- 239000000853 adhesive Substances 0.000 claims description 9
- 230000001070 adhesive effect Effects 0.000 claims description 9
- 239000004677 Nylon Substances 0.000 claims description 8
- 150000001993 dienes Chemical class 0.000 claims description 8
- 239000004744 fabric Substances 0.000 claims description 8
- 229920001778 nylon Polymers 0.000 claims description 8
- 229920001897 terpolymer Polymers 0.000 claims description 8
- 229920001169 thermoplastic Polymers 0.000 claims description 8
- 229920001400 block copolymer Polymers 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 7
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 7
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 229920002554 vinyl polymer Polymers 0.000 claims description 7
- ISAOUZVKYLHALD-UHFFFAOYSA-N 1-chloro-1,3,5-triazinane-2,4,6-trione Chemical compound ClN1C(=O)NC(=O)NC1=O ISAOUZVKYLHALD-UHFFFAOYSA-N 0.000 claims description 6
- 244000043261 Hevea brasiliensis Species 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 6
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 claims description 6
- 239000010410 layer Substances 0.000 claims description 6
- 229920003052 natural elastomer Polymers 0.000 claims description 6
- 229920001194 natural rubber Polymers 0.000 claims description 6
- 229920002755 poly(epichlorohydrin) Polymers 0.000 claims description 6
- 229920002647 polyamide Polymers 0.000 claims description 6
- 239000004417 polycarbonate Substances 0.000 claims description 6
- 229920000515 polycarbonate Polymers 0.000 claims description 6
- 229920002635 polyurethane Polymers 0.000 claims description 6
- 239000004814 polyurethane Substances 0.000 claims description 6
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinyl group Chemical group C1(O)=CC(O)=CC=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 6
- 238000012360 testing method Methods 0.000 claims description 6
- YRIZYWQGELRKNT-UHFFFAOYSA-N 1,3,5-trichloro-1,3,5-triazinane-2,4,6-trione Chemical compound ClN1C(=O)N(Cl)C(=O)N(Cl)C1=O YRIZYWQGELRKNT-UHFFFAOYSA-N 0.000 claims description 5
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 5
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 5
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 5
- 239000004615 ingredient Substances 0.000 claims description 5
- 229920000570 polyether Polymers 0.000 claims description 5
- 229920000874 polytetramethylene terephthalate Polymers 0.000 claims description 5
- 229950009390 symclosene Drugs 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 238000009833 condensation Methods 0.000 claims description 4
- 230000005494 condensation Effects 0.000 claims description 4
- 238000001816 cooling Methods 0.000 claims description 4
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 4
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
- 238000003466 welding Methods 0.000 claims description 4
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims description 3
- 239000012790 adhesive layer Substances 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 3
- 125000003368 amide group Chemical group 0.000 claims description 3
- CEJLBZWIKQJOAT-UHFFFAOYSA-N dichloroisocyanuric acid Chemical compound ClN1C(=O)NC(=O)N(Cl)C1=O CEJLBZWIKQJOAT-UHFFFAOYSA-N 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 235000010299 hexamethylene tetramine Nutrition 0.000 claims description 3
- 239000004312 hexamethylene tetramine Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 229960004011 methenamine Drugs 0.000 claims description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 3
- 229910017604 nitric acid Inorganic materials 0.000 claims description 3
- 230000003534 oscillatory effect Effects 0.000 claims description 3
- 229920000098 polyolefin Polymers 0.000 claims description 3
- 229920006324 polyoxymethylene Polymers 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 239000004753 textile Substances 0.000 claims description 3
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims description 2
- 229920002943 EPDM rubber Polymers 0.000 claims description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical group CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical group CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 239000002585 base Substances 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 2
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 claims description 2
- 229920001973 fluoroelastomer Polymers 0.000 claims description 2
- 239000002828 fuel tank Substances 0.000 claims description 2
- 229920001903 high density polyethylene Polymers 0.000 claims description 2
- 239000004700 high-density polyethylene Substances 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 230000006698 induction Effects 0.000 claims description 2
- 229920001684 low density polyethylene Polymers 0.000 claims description 2
- 239000004702 low-density polyethylene Substances 0.000 claims description 2
- 150000002924 oxiranes Chemical class 0.000 claims description 2
- 238000010422 painting Methods 0.000 claims description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- 229920003225 polyurethane elastomer Polymers 0.000 claims description 2
- 229920002981 polyvinylidene fluoride Polymers 0.000 claims description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
- 238000009987 spinning Methods 0.000 claims description 2
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 claims description 2
- 239000005708 Sodium hypochlorite Substances 0.000 claims 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 2
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 claims 2
- 229920003246 polypentenamer Polymers 0.000 claims 2
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 claims 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 claims 1
- 229920001038 ethylene copolymer Polymers 0.000 claims 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 239000000306 component Substances 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 239000011229 interlayer Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000004831 Hot glue Substances 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 238000002372 labelling Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- RCHKEJKUUXXBSM-UHFFFAOYSA-N n-benzyl-2-(3-formylindol-1-yl)acetamide Chemical compound C12=CC=CC=C2C(C=O)=CN1CC(=O)NCC1=CC=CC=C1 RCHKEJKUUXXBSM-UHFFFAOYSA-N 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/12—Bonding of a preformed macromolecular material to the same or other solid material such as metal, glass, leather, e.g. using adhesives
- C08J5/121—Bonding of a preformed macromolecular material to the same or other solid material such as metal, glass, leather, e.g. using adhesives by heating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C—APPARATUS FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C1/00—Apparatus in which liquid or other fluent material is applied to the surface of the work by contact with a member carrying the liquid or other fluent material, e.g. a porous member loaded with a liquid to be applied as a coating
- B05C1/003—Apparatus in which liquid or other fluent material is applied to the surface of the work by contact with a member carrying the liquid or other fluent material, e.g. a porous member loaded with a liquid to be applied as a coating incorporating means for heating or cooling the liquid or other fluent material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C—APPARATUS FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05C1/00—Apparatus in which liquid or other fluent material is applied to the surface of the work by contact with a member carrying the liquid or other fluent material, e.g. a porous member loaded with a liquid to be applied as a coating
- B05C1/04—Apparatus in which liquid or other fluent material is applied to the surface of the work by contact with a member carrying the liquid or other fluent material, e.g. a porous member loaded with a liquid to be applied as a coating for applying liquid or other fluent material to work of indefinite length
- B05C1/06—Apparatus in which liquid or other fluent material is applied to the surface of the work by contact with a member carrying the liquid or other fluent material, e.g. a porous member loaded with a liquid to be applied as a coating for applying liquid or other fluent material to work of indefinite length by rubbing contact, e.g. by brushes, by pads
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/26—Processes for applying liquids or other fluent materials performed by applying the liquid or other fluent material from an outlet device in contact with, or almost in contact with, the surface
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C65/00—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor
- B29C65/02—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure
- B29C65/06—Joining or sealing of preformed parts, e.g. welding of plastics materials; Apparatus therefor by heating, with or without pressure using friction, e.g. spin welding
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/01—General aspects dealing with the joint area or with the area to be joined
- B29C66/02—Preparation of the material, in the area to be joined, prior to joining or welding
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/71—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the composition of the plastics material of the parts to be joined
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/72—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined
- B29C66/723—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the structure of the material of the parts to be joined being multi-layered
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/73—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
- B29C66/737—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the state of the material of the parts to be joined
- B29C66/7375—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the state of the material of the parts to be joined uncured, partially cured or fully cured
- B29C66/73753—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the state of the material of the parts to be joined uncured, partially cured or fully cured the to-be-joined area of at least one of the parts to be joined being partially cured, i.e. partially cross-linked, partially vulcanized
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/73—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
- B29C66/737—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the state of the material of the parts to be joined
- B29C66/7375—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the state of the material of the parts to be joined uncured, partially cured or fully cured
- B29C66/73755—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset characterised by the state of the material of the parts to be joined uncured, partially cured or fully cured the to-be-joined area of at least one of the parts to be joined being fully cured, i.e. fully cross-linked, fully vulcanized
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C66/00—General aspects of processes or apparatus for joining preformed parts
- B29C66/70—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material
- B29C66/73—General aspects of processes or apparatus for joining preformed parts characterised by the composition, physical properties or the structure of the material of the parts to be joined; Joining with non-plastics material characterised by the intensive physical properties of the material of the parts to be joined, by the optical properties of the material of the parts to be joined, by the extensive physical properties of the parts to be joined, by the state of the material of the parts to be joined or by the material of the parts to be joined being a thermoplastic or a thermoset
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Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Lining Or Joining Of Plastics Or The Like (AREA)
- Laminated Bodies (AREA)
Description
(54) METHOD OF APPLYING A PLASTICS TO A VULCANIZED
RUBBER (7)1) We, DUNLOP LIMITED, a
British Company of Dunlop House, Ryder
Street, St. James's, London S.W.1, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement: - This invention relates to the application of thermoplastic plastics to vulcanized rubbers and is an improvement in or modification of
U.K. Patent Serial No. 1,4516,855.
According to the present invention, a method of applying a film of a thermoplastic plastics to the surface of a vulcanized rubber comprises causing relative frictional movement between the plastics and the rubber to melt the contact surface of the plastics, and moving the plastics and/or the rubber in relation to each other, whilst continuing said relative frictional movement, to leave a trail of the plastics on the rubber.
By this method, films of high or low strength plastics may be applied, e.g. as decoration, labelling, a potential hot-melt adhesive, or to confer desired properties on the rubber surface e.g. compatability with other materials or improvement of its ozone resistance.
The thermoplastic plastics may be in the form of a rod held in the chuck of a rotating or oscillating drill. When the surface of the rod in contact with the rubber has melted the rod is moved across the surface of the rubber so that a trail of the plastics is deposited. The rubber may be textile reinforced e.g. with nylon and if the surface to be moved relatively in contact with a plastics is uneven, it may be prebuffed.
The relative frictional movement between the plastics and the rubber may be produced in any convenient manner. One or both com- ponents may be moved. The friction may be achieved by rotary, angular or linear movement. The movement may be continuous, i.e.
in one direction, or oscillatory. An alternative to mechanical movement is the use of an ultrasonic frequency welding technique which creates rapid small vibratory movement between the surfaces.
The conditions of the relative frictional movement, such as speed and duration of the movement and pressure between the plastics and the rubber, are such as to melt the frictior surface of the plastics. A typical rate of frictional movement across a rubber is between 2.6 X 10-3 m/sec and 20.3 X 10 m/sec and a pressure of usually only about 100 to 500 kN/m2 for 1 to 10 seconds is required.
Of course, the conditions of application will depend on the materials used. Examples of suitable continuous relative rotary movement speeds are from 750 to 3000 revolutions per minute. When an oscillatory movement is employed, this may be performed over a few degrees of arc or, in the case of linear movement, over about 0.1-6 mm, preferably 1-4 mm, and at a frequency of 50--200 Hz, especially 100 Hz. External heating is not usually necessary but may be employed if desired.
Usually it is only necessary to raise the temperature of the plastics a few degrees above its melting point at its contact surface and therefore it can be cooled very rapidly and degradation of it or the substrate is unlikely.
The plastics and/or the rubber may be frozen to harden it for the relative frictional movement.
Separate films may be applied simultaneously by suitable equipment. Shaped films may be applied e.g. as a shoe outline by using e.g. linear or angular friction techniques.
Examples of compatible thermoplastic plastics film materials and vulcanized rubber substrates are: poly(vinyl chloride) with styrene/butadiene rubber; poly(ethylene terephthalate), poly (tetramethylene terephthalate), polar elastoplastic linear block copolymers containing polyester blocks and polyether blocks, or polyformaldehyde, with polyepichlorhydrin or epichlorhydrin/ethylene oxide rubber; polyamides (preferably those with 3 to 12 methylene groups between the amide groups) with polyepichlorhydrin, sulphur-cured polyurethane, nitrile rubber or styrene/butadiene rubber; polycarbonates with nitrile rubber or polyepichlorhydrin; vinyl chloride polymers or styrene/acrylonitrile copolymers with nitrile rubber; methylmethacrylate resin with polyepichlorhydrin; substantially linear crystalline low pressure solution olefin polymers e.g. high density polyethylene, polypropylene or a copolymer of ethylene and/or propylene and/or a minor amount of butene-l, hexene-l or a diene such as butadiene with ethylene/alphamonoolefin copolymer or ethylene/alphamonoolefin/diolefin terpolymer compositions containing up to 70% polymer; low density polyethylene or crystalline copolymers of ethylene with a vinyl alkanoic ester such as vinyl acetate, an alkyl acrylate such as ethyl acrylate or a vinyl halide such as vinyl chloride with ethylene/alpha-monoolefin copolymer or ethylene/alpha-monoolefin/diolefin terpolymer compositions containing up to 55% polymer; poly(ethylene terephthalate) or poly(tetramethylene terephthalate) with styrene/butadiene rubber, nitrile rubber or polybutadiene; polar elastoplastic linear block copolymers containing polyester blocks and polyether blocks with natural rubber, styrene/butadiene rubber, nitrile rubber, polyurethane rubber, acrylate rubber, polychloroprene, propylene oxide/unsaturated epoxide rubber or polybutadiene rubber; polyamides, preferably those with 3 to 12 methylene groups between the amide groups with vinylidene fluoride fluoroelastomers, natural rubber, polychloroprene, transpolypentenamer or polybutadiene rubber; polycarbonates with polybutadiene rubber; poly(vinylidene fluoride) with acrylate rubber; methyl methacrylate resin with nitrile rubber; poly ( chlorotrifluoroethylene ) with styrene/ butadiene rubber; and polyurethane plastics with styrene/butadiene rubber or natural rubber. The polycarbonate may be a polyester of
carbonic acid which is derived from dihydroxyl compounds in which the hydroxyl groups are directly attached to aromatic rings.
The rubber may be pre-treated i.e. treated before relative frictional movement with a plastics to enhance its adherability to the plastics film, for example the rubber may be pre-treated with a chemical treatment agent e.g. aldehyde condensation resin-forming ingredients such as resorcinol and hexamethylene tetramine, acidified sodium hyperchlorite, concentrated nitric acid, a chloro-isocyanuric acid such as trichloroisocyanuric acid suitably as a solution e.g. in ethyl acetate or as a powder, an alkali metal salt of a chloro-isocyanuric acid e.g. sodium dichloroisocyanurate, (such salts are commercially available under the trade name 'Fi-clor'), UV irradiation, glow discharge or flame-treatment. The term 'aldehyde condensation resin-forming ingredients' as used in this specification includes a partially condensed aldehyde resin. Alternatively and preferably a chemical treatment agent can be applied 'in situ' as the plastics film is applied to the rubber. This can be done either by forming or drilling at least one cavity in the plastics body and packing the cavities with a treatment agent or by forming into the required shape e.g. by moulding a blend of a plastics material and a treatment agent such as one of those already mentioned.
If desired the treatment agent may be supported in an inert medium e.g. a wax. When the plastics is in the form of a rod the cavity or cavities preferably extend longitudinally of the rod.
The plastics and/or the rubber may be in a compound with conventional ingredients such as plasticisers, tackifiers, softeners, fillers, pigments, antioxidants and stabilisers.
Incompatible substrates e.g. vulcanized nitrile rubber and vulcanized polychloroprene rubber may be bonded by applying a plastics film to each of them by the method of the present invention and then bonding the films e.g. by melting at least one of them and allowing the film or films to solidify in contact.
Alternatively, a plastics interlayer may be placed between the film coated substrates and then the interlayer and usually also the films are melted and the assembly is allowed to cool.
The method of the present invention may be used in the manufacture of footwear. It is generally recognised that vulcanized rubber is the most durable material for footwear soles.
The sole has to be attached to the upper of the article of footwear and previously this has uusually been done using an adhesive. If the adhesive is based on a conventional rubber solution e.g. one based on polychloroprene, this usually must be coated onto the sole and upper and allowed to dry to a slightly tacky state before the two components are pressed together. If a polyurethane-based adhesive is used, this must usually be coated onto both components and dried completely before bonding. The adhesive layer on the sole is then softened, e.g. using an infra red lamp, and the two components are pressed together. Both these methods are time-consuming because adhesive must be applied to sole and upper individually and the solvent in the adhesive allowed to evaporate before contacting the sole and upper. In addition it is usual to buff the adhering surfaces of the sole and upper before applying an adhesive.
It is proposed to have a sole comprising a base of a vulcanized rubber composition having a layer or layers of a thermoplastic plastics bonded to it by the method of the present invention at places where the sole will eventually be attached to an upper. In order to attach the sole to an upper it is usually only necessary to soften at least the surface of the plastics, e.g. by infra red, ultrasonic, radio frequency or induction heating methods, and press the softened surface against the upper.
Alternatively the surface of the plastics may be melted by using a friction welding tool. On cooling, a bond is obtained between the sole and the upper. No messy solvents are involved, and the process of bonding the upper to the sole is quicker and easier as it is not necessary to apply an adhesive to both sole and upper.
Another advantage is that a sole can be easily transported already having a potential adhesive layer which can be bonded to an upper when required. It is also possible to use compositions for a sole based on rubbers which could not be used previously because they could not be bonded satisfactorily to an upper, e.g. a saturated ethylene/propylene copolymer rubber (commonly called EPM) or an unsaturated ethylene/propylene/diene terpolymer rubber (commonly called EPDM) e.g. an ethylene/ propylene/ethylidene norboruene terpolymer rubber.
Examples of other applications of the method of the present invention are in the fabrication of rubber or rubberized containers, harnessing, furniture, belting and hose and in the retreading od tires.
The invention will now be iliustrated in the following Examples:
EXAMPLE I.
Two sheets of rubber covered nylon fabric having a nitrile rubber composition on one side and a Neoprene composition on the other side manufactured by Dunlop Limited for flexible fuel tanks were positioned such that in one case the nitrile rubber compound (5635) and in the other the neoprene compound (5632) was facing upwards. A corresponding strip od at least 38 mm width on each sheet was buffed with a normal hand held sanding disc.
Against each buffed strip a rod measuring approximately 19 mm diameter by 30 mm long of a polar elastoplastic linear block copolymer containing polyester and polyester ether blocks and available as Hytrel 4055 from
Du Pont was spun at 3000 rpm under a load of approximately 45 newtons down each edge such that at least 25.4 mm width was covered with a thin layer of Hytrel 4055. This was done by pulling each sheet under the molten end of the spinning plastics rod at a speed of 1 metre/minute.
One strip of fabric 50.8 mm wide was cut from each sheet at right angles to the frictioned edge. A sheet of Hytrel 4055 measuring 25.4 mm X 50.8 mm X 0.125 mm was placed between the two frictioned ends of the strips arranged to overlap a distance of 25.4 mm.
The strips were positioned such that on testing the bond would be loaded in shear.
The overlap was placed in a press at 1900C with sufficient pressure to hold the two ends together. After 60 seconds the press was cooled until the Hytrel had solidified. The bonded strips were tested on a 10 ton Avery Universal
Test Machine and failed at a force of 3380 newtons. Failure occurred in the fabric.
EXAMPLE II.
Example I was repeated except that the two neoprene surfaces were bonded together. The test piece failed at 2580 newtons with failure in the fabric.
EXAMPLE III.
The top edge of a standard styrene/butadiene rubber based wellington boot was frictioned as described in Example I, but against a rigid polyvinyl chloride (PVC) rod instead of Hytrel and the rubber surface had been pre-treated by painting with a 3% weight/ volume solution of Fi-dor 91 (Trichloroisocyanuric acid) in ethyl acetate. A sheet of nylon reinforced polyvinyl chloride was then welded to the PVC coated rubber by means of a 3+ KW Radyne Radio Frequency welder.
The current was maintained until the PVC was seen to melt. On cooling the nylon reinforced polyvinyl chloride sheet was firmly attached to the rubber boot material with sufficient bond strength as to cause rubber failure when the bond was tested.
"FI-CLOR", "HYTREL", "AVERY" and "RADYNE" are Registered Trade Marks.
WHAT WE CLAIM IS:
1. A method of applying a film of a thermoplastic plastics to the surface of a vulcanized rubber which comprises causing relative frictional movement between the plastics and the rubber to melt the contact surface of the plas
tics, and moving the plastics and/or the rubber in relation to each other, whilst continuing said relative frictional movement, to leave a trail of the plastics on the rubber.
2. A method according to claim 1 wherein the plastics and rubber are selected from the
following groups viz. poly(vinyl chloride) with
styrene/butadiene rubber, poly(ethylene terephthalate) or poly(tetra-methylene terephthalate) with nitrile rubber; poly(ethylene terephthalate), poly(tetramethylene terephthalate), polar elastoplastic linear block copolymers containing polyester blocks and polyether blocks, or polyformaldehyde with polyepichlorohydrin or epichlorohydrin/ethylene
oxide rubber; polyamides with polyepichlorohydrin, sulphur-cured polyurethane, nitrile
rubber or styrene/butadiene rubber; poly
**WARNING** end of DESC field may overlap start of CLMS **.
Claims (1)
- **WARNING** start of CLMS field may overlap end of DESC **.applying an adhesive.It is proposed to have a sole comprising a base of a vulcanized rubber composition having a layer or layers of a thermoplastic plastics bonded to it by the method of the present invention at places where the sole will eventually be attached to an upper. In order to attach the sole to an upper it is usually only necessary to soften at least the surface of the plastics, e.g. by infra red, ultrasonic, radio frequency or induction heating methods, and press the softened surface against the upper.Alternatively the surface of the plastics may be melted by using a friction welding tool. On cooling, a bond is obtained between the sole and the upper. No messy solvents are involved, and the process of bonding the upper to the sole is quicker and easier as it is not necessary to apply an adhesive to both sole and upper.Another advantage is that a sole can be easily transported already having a potential adhesive layer which can be bonded to an upper when required. It is also possible to use compositions for a sole based on rubbers which could not be used previously because they could not be bonded satisfactorily to an upper, e.g. a saturated ethylene/propylene copolymer rubber (commonly called EPM) or an unsaturated ethylene/propylene/diene terpolymer rubber (commonly called EPDM) e.g. an ethylene/ propylene/ethylidene norboruene terpolymer rubber.Examples of other applications of the method of the present invention are in the fabrication of rubber or rubberized containers, harnessing, furniture, belting and hose and in the retreading od tires.The invention will now be iliustrated in the following Examples: EXAMPLE I.Two sheets of rubber covered nylon fabric having a nitrile rubber composition on one side and a Neoprene composition on the other side manufactured by Dunlop Limited for flexible fuel tanks were positioned such that in one case the nitrile rubber compound (5635) and in the other the neoprene compound (5632) was facing upwards. A corresponding strip od at least 38 mm width on each sheet was buffed with a normal hand held sanding disc.Against each buffed strip a rod measuring approximately 19 mm diameter by 30 mm long of a polar elastoplastic linear block copolymer containing polyester and polyester ether blocks and available as Hytrel 4055 from Du Pont was spun at 3000 rpm under a load of approximately 45 newtons down each edge such that at least 25.4 mm width was covered with a thin layer of Hytrel 4055. This was done by pulling each sheet under the molten end of the spinning plastics rod at a speed of 1 metre/minute.One strip of fabric 50.8 mm wide was cut from each sheet at right angles to the frictioned edge. A sheet of Hytrel 4055 measuring 25.4 mm X 50.8 mm X 0.125 mm was placed between the two frictioned ends of the strips arranged to overlap a distance of 25.4 mm.The strips were positioned such that on testing the bond would be loaded in shear.The overlap was placed in a press at 1900C with sufficient pressure to hold the two ends together. After 60 seconds the press was cooled until the Hytrel had solidified. The bonded strips were tested on a 10 ton Avery Universal Test Machine and failed at a force of 3380 newtons. Failure occurred in the fabric.EXAMPLE II.Example I was repeated except that the two neoprene surfaces were bonded together. The test piece failed at 2580 newtons with failure in the fabric.EXAMPLE III.The top edge of a standard styrene/butadiene rubber based wellington boot was frictioned as described in Example I, but against a rigid polyvinyl chloride (PVC) rod instead of Hytrel and the rubber surface had been pre-treated by painting with a 3% weight/ volume solution of Fi-dor 91 (Trichloroisocyanuric acid) in ethyl acetate. A sheet of nylon reinforced polyvinyl chloride was then welded to the PVC coated rubber by means of a 3+ KW Radyne Radio Frequency welder.The current was maintained until the PVC was seen to melt. On cooling the nylon reinforced polyvinyl chloride sheet was firmly attached to the rubber boot material with sufficient bond strength as to cause rubber failure when the bond was tested."FI-CLOR", "HYTREL", "AVERY" and "RADYNE" are Registered Trade Marks.WHAT WE CLAIM IS:1. A method of applying a film of a thermoplastic plastics to the surface of a vulcanized rubber which comprises causing relative frictional movement between the plastics and the rubber to melt the contact surface of the plas tics, and moving the plastics and/or the rubber in relation to each other, whilst continuing said relative frictional movement, to leave a trail of the plastics on the rubber.2. A method according to claim 1 wherein the plastics and rubber are selected from the following groups viz. poly(vinyl chloride) with styrene/butadiene rubber, poly(ethylene terephthalate) or poly(tetra-methylene terephthalate) with nitrile rubber; poly(ethylene terephthalate), poly(tetramethylene terephthalate), polar elastoplastic linear block copolymers containing polyester blocks and polyether blocks, or polyformaldehyde with polyepichlorohydrin or epichlorohydrin/ethylene oxide rubber; polyamides with polyepichlorohydrin, sulphur-cured polyurethane, nitrile rubber or styrene/butadiene rubber; polycarbonates with nitrile rubber or polyepichlorohydrin; vinyl chloride polymers or styrene/ acrylonitrile copolymers with nitrile rubber; methylmethacrylate resin with polyepichlorohydrin; substantially linear crystalline low pressure solution polymerised olefin polymers with ethylene/alpha-monoolefin copolymer or ethylene/alpha-monoolefin/diolefin terpolymer compositions containing up to 70% polymer; low density polyethylene or crystalline copolymers of ethylene with a vinyl alkanoic ester, an alkyl acrylate or a vinyl halide with ethylene/alpha-monolefin copolymer or ethylene/alpha-monolefin/diolefin terpolymer compositions containing up to 55% polymer; poly(ethylene terephthalate) or poly(tetramethylene terephthalate) with styrene/butadiene rubber or polybutadiene; polar elastoplastic linear block copolymers containing polyester blocks and polyether blocks with trans-polypentenamer, natural rubber, styrene/ butadiene rubber, nitrile rubber, polyurethane rubber, acrylate rubber, polychloroprene, pTO- pylene oxide/unsaturated epoxide rubber or polybutadiene rubber; polyamides with vinylidene fluoride fluoro-elastomers, natural rubber, polychloroprene, trans-polypentenamer or polybutadiene rubber; polycarbonates with polybutadiene rubber; poly( vinylidene fluoride) with acrylate rubber; methyl methacrylate resin with nitrile rubber, poly(chlorotrifluoro- ethylene) with styrene/butadiene rubber; and polyurethane plastics with styrene/butadiene rubber or natural rubber.3. A method according to claim 2 wherein the substantially linear crystalline low pressure solution polymerised olefin polymer is high density polyethylene, polypropylene or copolymer of ethylene or propylene with each other or with a minor amount of butene-l, hexene- 1 or a diene, the vinyl alkanoic ester is vinyl acetate, the alkyl acrylate is ethyl acrylate, the vinyl halide of the ethylene copolymer is vinyl chloride, the polyamide has from 3 to 12 methylene groups between the amide groups, the polycarbonate is a polyester of carbonic acid which is derived from dihydroxyl compounds in which the hydroxyl groups are directly attached to aromatic rings, and the vinyl chloride polymer is poly(vinyl chloride), poly( vinyl dichloride) or poly(vinylidene chloride).4. A method according to claim 1, 2 or 3 wherein the relative frictional movement is rotary, angular or linear mechanical movement.5. A method according to claim 1, 2 or 3 wherein the relative frictional movement is produced by an ultrasonic frequency welding technique.6. A method according to any of claims 1 to 5 wherein the surface of the rubber to be bonded is pretreated with UV irradiation, glow discharge or flame treatment.7. A method according to any preceding claim wherein the plastics and rubber are moved in relation to each other for from 1 to 10 seconds and the pressure between them during the relative movement is from 100 to 500 kN/m2.8. A method according to any preceding claim wherein the relative frictional movement is continuous rotary movement at from 750 to 3000 revolutions per minute.9. A method according to any of claims 1 to 7 wherein the relative frictional movement is oscillatory linear movement at a frequency of from 50 to 200 Hz.10. A method according to any preceding claim wherein the vulcanized rubber is in the form of a footwear sole.11. A method according to any preceding claim wherein the surface of the rubber to be bonded is pretreated with a chemical treatment agent.12. A method according to claim 11 wherein the treatment agent is selected from concentrated nitric acid, acidified sodium hypochlorite, trichloroisocyanuric acid and sodium dichloroisocyanurate.13. A method according to claim 11 wherein the treatment agent is selected from aldehyde condensation resin-forming ingredients, a hypochlorous acid generator, a chloroisocyanuric acid and an alkali metal salt of a chloroisocyanuric acid.14. A method according to claim 13 wherein the treatment agent is resorcinol and hexamethylene tetramine.15. A method according to any of claims 1 to 10 wherein the surface of the rubber is treated with a treatment agent as the plastics film is applied to it.16. A method according to claim 15 wherein the treatment agent is in the form of a blend with the plastics.d7. A method according to claim 15 wherein the treatment agent is contained in at least one cavity in the plastics.118. A method according to claim 17 wherein plastics is in the form of a rod and the or each cavity extends longitudinally of the plastics rod.19. A method according to claim 17 or 18 wherein the treatment agent is supported in an inert medium.20. A method according to claim 19 wherein the inert medium is a wax.21. A method according to any of claims 15 to 20 wherein the treatment agent is selected from aldehyde condensation resinforming ingredients, a hypochlorous acid generator, concentrated nitric acid, a chloro- isocyanuric acid and an alkali metal salt of a chloro-isocyanuric acid.22. A method according to claim 21 wherein the treatment agent is selected from resorcinol and hexamethylene tetramine, acidified sodium hypochlorite, trichloroisocyanuric acid and sodium dichloroisocyanurate.23. A method according to any preceding claim wherein the plastics is poly(vinyl chloride) and the rubber is styrene/lbutadiene rubber.24. A method according to any preceding claim wherein the plastics and/or rubber is frozen to harden it for the relative frictional movement.15. A method according to any preceding claim wherein the rubber is textile reinforced.26. A method according to claim 25 wherein the textile is nylon.27. A method of producing a plastics-filmcoated vulcanized rubber according to claim 1 substantially as described in any one of the Examples.28. A method of producing a plastics-filmcoated vulcanized rubber according to claim 1 substantially as described herein.29. A plastics-film-coated vulcanized rubber when made by the method according to any of the preceding claims.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB14208/76A GB1579433A (en) | 1973-03-09 | 1976-04-07 | Method of applying a plastics to a vulcanized rubber |
ZA00771891A ZA771891B (en) | 1976-04-07 | 1977-03-29 | Method of applying a plastics film to a vulcanised rubber |
AU23866/77A AU2386677A (en) | 1976-04-07 | 1977-04-01 | Applying a plastics film to a vulcanised rubber |
IT2205477A IT1114772B (en) | 1976-04-07 | 1977-04-04 | Applying thermoplastics film to vulcanised rubber surface - by frictional movement between them causing melting |
JP3995877A JPS52123475A (en) | 1976-04-07 | 1977-04-07 | Method of coating plastic on vulcanized rubber |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1159173A GB1456855A (en) | 1973-03-09 | 1973-03-09 | Method of producing rubber-plastics composites |
GB14208/76A GB1579433A (en) | 1973-03-09 | 1976-04-07 | Method of applying a plastics to a vulcanized rubber |
GB1989076 | 1976-05-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1579433A true GB1579433A (en) | 1980-11-19 |
Family
ID=27256702
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14208/76A Expired GB1579433A (en) | 1973-03-09 | 1976-04-07 | Method of applying a plastics to a vulcanized rubber |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1579433A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0298869A1 (en) * | 1987-07-10 | 1989-01-11 | Souriau Et Cie | Method of joining parts of polymeric material |
FR2639520A1 (en) * | 1988-11-25 | 1990-06-01 | Ebauchesfabrik Eta Ag | PLASTIC BRACELET |
WO2003013737A1 (en) * | 2001-08-08 | 2003-02-20 | Henkel Kommanditgesellschaft Auf Aktien | Device and method for applying a solid substance that can be applied by the action of heat |
WO2014161745A1 (en) * | 2013-04-03 | 2014-10-09 | Astrium Sas | Welded structural link between a high-performance thermoplastic matrix composite material and an elastomer by functionalisation in powder mode |
-
1976
- 1976-04-07 GB GB14208/76A patent/GB1579433A/en not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0298869A1 (en) * | 1987-07-10 | 1989-01-11 | Souriau Et Cie | Method of joining parts of polymeric material |
FR2617760A1 (en) * | 1987-07-10 | 1989-01-13 | Souriau & Cie | METHOD FOR ASSEMBLING PARTS IN POLYMERIC MATERIALS |
FR2639520A1 (en) * | 1988-11-25 | 1990-06-01 | Ebauchesfabrik Eta Ag | PLASTIC BRACELET |
EP0375918A1 (en) * | 1988-11-25 | 1990-07-04 | Eta SA Fabriques d'Ebauches | Plastic strap |
WO2003013737A1 (en) * | 2001-08-08 | 2003-02-20 | Henkel Kommanditgesellschaft Auf Aktien | Device and method for applying a solid substance that can be applied by the action of heat |
WO2014161745A1 (en) * | 2013-04-03 | 2014-10-09 | Astrium Sas | Welded structural link between a high-performance thermoplastic matrix composite material and an elastomer by functionalisation in powder mode |
FR3004187A1 (en) * | 2013-04-03 | 2014-10-10 | Astrium Sas | STRUCTURAL BOND SOLD BETWEEN HIGH-PERFORMANCE THERMOPLASTIC MATRIX COMPOSITE MATERIAL AND ELASTOMER USING POWDER FUNCTIONALIZATION |
US10118342B2 (en) | 2013-04-03 | 2018-11-06 | Arianegroup Sas | Welded structural joint between a high-performance thermoplastic matrix composite material and an elastomer by powder functionalization |
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PCNP | Patent ceased through non-payment of renewal fee |