EP3481882A1 - Tiges de chaussures - Google Patents
Tiges de chaussuresInfo
- Publication number
- EP3481882A1 EP3481882A1 EP17742658.2A EP17742658A EP3481882A1 EP 3481882 A1 EP3481882 A1 EP 3481882A1 EP 17742658 A EP17742658 A EP 17742658A EP 3481882 A1 EP3481882 A1 EP 3481882A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- chain
- tpu
- monomer
- diisocyanate
- upper according
- 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.)
- Withdrawn
Links
- 229920000642 polymer Polymers 0.000 claims abstract description 49
- 239000000203 mixture Substances 0.000 claims abstract description 18
- 239000000178 monomer Substances 0.000 claims description 47
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 20
- -1 aromatic diol Chemical class 0.000 claims description 13
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims description 11
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 7
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 150000002009 diols Chemical class 0.000 claims description 6
- 229920002635 polyurethane Polymers 0.000 claims description 5
- 239000004814 polyurethane Substances 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 4
- VDHWOHDSOHPGPC-UHFFFAOYSA-N 3,3-dihydroxyoxepan-2-one Chemical compound OC1(O)CCCCOC1=O VDHWOHDSOHPGPC-UHFFFAOYSA-N 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 claims description 3
- 239000004014 plasticizer Substances 0.000 claims description 3
- ZXHZWRZAWJVPIC-UHFFFAOYSA-N 1,2-diisocyanatonaphthalene Chemical compound C1=CC=CC2=C(N=C=O)C(N=C=O)=CC=C21 ZXHZWRZAWJVPIC-UHFFFAOYSA-N 0.000 claims description 2
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 2
- 125000005442 diisocyanate group Chemical group 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 229940093476 ethylene glycol Drugs 0.000 claims description 2
- 239000012948 isocyanate Substances 0.000 claims description 2
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims description 2
- 229920001610 polycaprolactone Polymers 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims description 2
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 claims description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 abstract description 80
- 239000004433 Thermoplastic polyurethane Substances 0.000 abstract description 77
- 239000010410 layer Substances 0.000 description 30
- 238000000034 method Methods 0.000 description 12
- 238000012360 testing method Methods 0.000 description 12
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000003466 welding Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 3
- 238000010186 staining Methods 0.000 description 3
- 210000003371 toe Anatomy 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 210000002683 foot Anatomy 0.000 description 2
- 125000001475 halogen functional group Chemical group 0.000 description 2
- 229960004592 isopropanol Drugs 0.000 description 2
- 239000004745 nonwoven fabric Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 244000056139 Brassica cretica Species 0.000 description 1
- 235000003351 Brassica cretica Nutrition 0.000 description 1
- 235000003343 Brassica rupestris Nutrition 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- NSPSPMKCKIPQBH-UHFFFAOYSA-K bismuth;7,7-dimethyloctanoate Chemical compound [Bi+3].CC(C)(C)CCCCCC([O-])=O.CC(C)(C)CCCCCC([O-])=O.CC(C)(C)CCCCCC([O-])=O NSPSPMKCKIPQBH-UHFFFAOYSA-K 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000012936 correction and preventive action Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000005304 joining Methods 0.000 description 1
- 235000008960 ketchup Nutrition 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 235000010460 mustard Nutrition 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A43—FOOTWEAR
- A43B—CHARACTERISTIC FEATURES OF FOOTWEAR; PARTS OF FOOTWEAR
- A43B23/00—Uppers; Boot legs; Stiffeners; Other single parts of footwear
- A43B23/02—Uppers; Boot legs
- A43B23/0205—Uppers; Boot legs characterised by the material
- A43B23/0225—Composite materials, e.g. material with a matrix
-
- A—HUMAN NECESSITIES
- A43—FOOTWEAR
- A43B—CHARACTERISTIC FEATURES OF FOOTWEAR; PARTS OF FOOTWEAR
- A43B23/00—Uppers; Boot legs; Stiffeners; Other single parts of footwear
- A43B23/02—Uppers; Boot legs
- A43B23/0205—Uppers; Boot legs characterised by the material
- A43B23/0215—Plastics or artificial leather
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D35/00—Producing footwear
- B29D35/12—Producing parts thereof, e.g. soles, heels, uppers, by a moulding technique
- B29D35/126—Uppers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/22—Catalysts containing metal compounds
- C08G18/227—Catalysts containing metal compounds of antimony, bismuth or arsenic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3203—Polyhydroxy compounds
- C08G18/3206—Polyhydroxy compounds aliphatic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
- C08G18/44—Polycarbonates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5003—Polyethers having heteroatoms other than oxygen having halogens
- C08G18/5015—Polyethers having heteroatoms other than oxygen having halogens having fluorine atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/73—Polyisocyanates or polyisothiocyanates acyclic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
- C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
- C08G18/7671—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups containing only one alkylene bisphenyl group
Definitions
- the present invention relates to an upper for a footwear article, said upper comprising at least one panel having at least one layer made from a composition comprising a fluorinated thermoplastic polyurethane polymer.
- Uppers for footwear articles are generally formed by stitching together a plurality of exterior panel sections.
- These exterior panel sections can be made of several materials, such as natural and leather, plastic, mesh and non-woven fabrics.
- Non-woven fabrics are defined as fabric-like materials made from long fibers, bonded together by chemical, mechanical, heat or solvent treatment. The term is used in the textile manufacturing industry to denote fabrics, such as felt, which are neither woven nor knitted.
- the long fibers consists of hydrogenated thermoplastic polymers, notably based on hydrogenated urethane (H-TPU).
- H-TPU polymers have been disclosed in the art for the manufacturing of the upper part of shoes, for example in US 20100186874 PUMA AKTIENGESELLSCHAFT RUDOLF DASSLER SPORT , US 2013/0169219 PUMA SE and US 2014/0082961 REEBOK INTERNATIONAL LIMITED .
- Heat processable elastomeric polyurethanes comprising (per)fluoropoly- ether blocks were disclosed for example in US 5332798 AUSIMONT S.P.A. .
- the Applicant perceived the need of providing a new polymeric material that can be useful for the manufacture of the upper of footwear articles, notably shoes and boots, characterized by having improved properties when compared to hydrogenated thermoplastic polyurethane polymers (TPU). More in particular, the Applicant focused on providing a polymeric material having improved resistance to stain, improved chemical and wear resistance, low temperature flexibility, silky feel while maintaining good mechanical properties.
- TPU hydrogenated thermoplastic polyurethane polymers
- the present invention relates to an upper, for a footwear article, comprising at least one panel having at least one layer [layer E] made from a composition [composition (C)] comprising at least one fluorinated polyurethane [F-TPU polymer], said F-TPU polymer comprising recurring units derived from: [monomer (a)] at least one diol selected from the group comprising poly-ether type diol, poly-ester type diol, polybutadien-diol and polycarbonate-diol; [monomer (b)] at least one hydroxy-terminated (per)fluoropolyether polymer [PFPE polymer] ; [monomer (c)] at least one aromatic, aliphatic or cycloaliphatic diisocyanate; and [monomer (d)] at least one aliphatic, cycloaliphatic or aromatic diol having from 1 to 14 carbon atoms.
- composition (C)] comprising at least one fluorin
- said panel comprises layer E as single layer
- the Applicant has surprisingly found that when layer E is the outermost layer, it provides a soft silky feeling to the touch, without the addition of plasticizer agents to said composition (C).
- the upper can be manufactured using only one panel or joining together more than one panels.
- the panels can be selected from for example the toe box, the toe cap, the quarter, the vamp, the tongue, the counter and the back strap of a footwear.
- said F-TPU polymer has an average number molecular weight of from 30,000 to about 70,000 Da.
- said F-TPU polymer has a melting point (T m ) of from about 120°C to about 240°C.
- said at least one monomer (b) is a hydroxy-terminated (per)fluoropolyether polymer [PFPE polymer], i.e. a polymer comprising a (per)fluoropolyoxyalkylene chain [chain (R pf )] having two chain ends, wherein one or both chain ends terminates with at least one -OH group.
- PFPE polymer hydroxy-terminated (per)fluoropolyether polymer
- said chain (R pf ) is a chain of formula -O-D-(CFX # ) z1 -O(R f )(CFX * ) z2 -D*-O- wherein z1 and z2, equal or different from each other, are equal to or higher than 1;
- D and D*, equal or different from each other are an alkylene chain comprising from 1 to 6 and even more preferably from 1 to 3 carbon atoms, said alkyl chain being optionally substituted with at least one perfluoroalkyl group comprising from 1 to 3 carbon atoms;
- (R f ) comprises, preferably consists of, repeating units R°, said repeating units being independently selected from the group consisting of: (i) -CFXO-, wherein X
- said PFPE polymer complies with the following formula (PFPE-I): HO-(CH 2 CH 2 O) t -CH 2 -(R pf )-CH 2 (OCH 2 CH 2 ) u -OH (PFPE-I) wherein t and u are, each independently, 0 or from 1 to 5; and R pf is as defined above.
- said PFPE polymer has an average number molecular weight of from 400 to 10,000 Da, more preferably from 1,000 to 5,000.
- the molar ratio between monomers (a) and monomers (b) is from 2 to 20, more preferably from 2 to 10.
- the amount of monomers (b) is such that the F-TPU polymer comprises from 4 to 30 wt.% of fluorine.
- said at least one monomer (c) has a number molecular weight of 500 Da or lower, preferably from 10 to 500 Da.
- said at least one monomer (c) is selected in the group comprising, preferably consisting of, 4,4’-methylene-diphenylene-di- isocyanate (MDI), 1,6-hexan-diisocyanate (HDI), 2,4-toluene-diisocyanate, 2,6-toluene-diisocyanate, xylilen-diisocyanate, naphthalene-diisocyanate, paraphenylen-diisocyana- te, hexamaethylen-diisocyanate, isophorone-diisocyanate, 4,4’-dicyclohexyl-methane-diisocyanate and cyclohexyl-1,4-diisocyanate. MDI and HDI being particularly preferred.
- the sum of blocks deriving from monomers (c) and (d) is from 10 to 60 wt.% based on the total weight of the F-TPU polymer.
- blocks comprising recurring units derived from monomers (a) and (b) are rubber-like blocks, while blocks comprising recurring units derived from monomers (c) and (d) are hard blocks.
- At least 80% of the blocks comprising recurring units derived from said monomers (b) [blocks B] are linked, at least one of their ends, to a block comprising recurring units derived from monomers (a) [blocks A] through a block comprising recurring units derived from monomers (c) [blocks C].
- at least 80% of blocks B are contained in a sequence of the following type: -[A-C-B-C]-.
- the F-TPU polymer can be prepared following the procedures disclosed in US 5332798 AUSIMONT S.P.A. , in particular in Example 15.
- composition (C) can optionally comprise further additives, such as for example antioxidants, thermal stabilizers, dyestuffs and fillers.
- composition (C) is essentially made of said F-TPU polymer in combination with an amount of up to 1 wt.% of any of the additives listed above are also encompassed by the present invention.
- said upper comprises a plurality of panels stitched together, each panel comprising a layer E as defined above.
- said upper comprises one single panel, which extends for the entire surface of the upper and comprises a layer E as defined above.
- Uppers comprising one single panel are also known as “unitary upper design”.
- Layer E can be manufactured following methods known in the art, for example by melt-blown process as disclosed in US 2010/0186874 cited above
- step (iv) comprises two steps, wherein the first step comprises heating at a first temperature for a time from 10 seconds to 10 minutes and the second step comprises heating at a second temperature, said second temperature being lower than said first temperature, for a time of from 30 seconds to 24 hours.
- said first temperature is from 120°C to 300°C.
- said second temperature is from 50°C to 200°C.
- said at least one panel comprises layer E as the only layer.
- said at least one panel comprises layer E as defined above and at least one texture layer [layer T] consisting of texture yarns.
- the upper according to the present invention comprises at least one panel comprising layer E as defined above, said layer E having an external surface and an internal surface, wherein at least a part of said internal surface is connected with a texture layer [layer T] consisting of texture yarns.
- the upper according to the present invention comprises at least one panel comprising layer E as defined above and two layers T consisting of texture yarns, wherein layer E is interposed between two layers T.
- the upper comprises layer E and layer(s) T
- the upper is obtained by welding together layer E and layer(s) T.
- the welding can be performed for example using a high-frequency welding process or an ultrasonic sound welding process.
- the present invention relates to a footwear article comprising an upper as defined above.
- F-TPU polymer specimens Preparation of F-TPU polymer specimens – method A F-TPU polymer specimens 1 to 4 in the form of sheet were prepared starting from the abovementioned monomers following the same procedure detailed in Example 15 of US 5,332,798 (to Ausimont S.p.A.) cited above. F-TPU polymers thus obtained contained 20 wt.% of recurring units derived from monomers (b).
- H-TPU 9* a commercially available hydrogenated TPU
- the monomers ratio for H-TPU 9* is not publicly available.
- Table 1 Monomers (ratio by mol) a1 a2 a3 a4 b1 b2 c1 c2 d1 d2 F-TPU 1 0.8 - - - 0.2 - 2.0 - 1.0 - F-TPU 2 - 0.7 - - 0.3 - 3.0 - 2.0 - F-TPU 3 - 0.6 - - - 0.4 2.5 - 1.5 - F-TPU 4 - - - 0.75 0.25 - - 2.0 - 1.0 F-TPU 5 0.75 - - - - 0.25 - 3.0 2.0 - F-TPU 6 - - 0.75 - - 0.25 - 2.0 1.0 - F-TPU 7 4.0 - - - - 0.3 - 0.7 3.0 - H-TPU 8(
- Tests were performed once with dry denim and once with wet denim on F-TPU 1, F-TPU 2, F-TPU 3, F-TPU 5 and F-TPU 7.
- the tests were performed as follows: a denim sample measuring approximately 30 mm x 30 mm was fixed to a fixture in order to prevent shifting of the sample during the test. A sample of each F-TPU and of H-TPU was then placed on the denim sample and fixed to the fixture as well.
- a drop of each staining agent listed above was put into contact with the surface of a specimen made from F-TPU 1 and let for 24 hours at ambient conditions. The specimen was then cleaned with water.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Composite Materials (AREA)
- Polyurethanes Or Polyureas (AREA)
- Footwear And Its Accessory, Manufacturing Method And Apparatuses (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
Abstract
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP16178295 | 2016-07-07 | ||
| PCT/EP2017/066581 WO2018007359A1 (fr) | 2016-07-07 | 2017-07-04 | Tiges de chaussures |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP3481882A1 true EP3481882A1 (fr) | 2019-05-15 |
Family
ID=56372782
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP17742658.2A Withdrawn EP3481882A1 (fr) | 2016-07-07 | 2017-07-04 | Tiges de chaussures |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20200221825A1 (fr) |
| EP (1) | EP3481882A1 (fr) |
| JP (1) | JP2019523043A (fr) |
| KR (1) | KR20190024951A (fr) |
| CN (1) | CN109476810A (fr) |
| WO (1) | WO2018007359A1 (fr) |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1252660B (it) | 1991-12-23 | 1995-06-20 | Ausimont Spa | Poliuretani e poliuretani-uree fluorurati e processi per la loro preparazione |
| DE69918815T2 (de) * | 1998-03-05 | 2005-08-18 | Omnova Solutions Inc., Fairlawn | Einfach reinigbare polymere mehrschichtstoffe |
| US6342544B1 (en) * | 1999-04-14 | 2002-01-29 | Nike, Inc. | Durable outsole for article of footwear |
| US8544191B2 (en) | 2007-04-10 | 2013-10-01 | Reebok International Limited | Smooth shoe uppers and methods for producing them |
| JP5595910B2 (ja) * | 2007-07-18 | 2014-09-24 | ソルヴェイ・スペシャルティ・ポリマーズ・イタリー・エッセ・ピ・ア | フッ素を含有する芳香族水素化ポリマー |
| DE102007035729A1 (de) | 2007-07-30 | 2009-02-05 | Puma Aktiengesellschaft Rudolf Dassler Sport | Verfahren zum Herstellen eines Schuhoberteils |
| US9417677B2 (en) | 2011-12-29 | 2016-08-16 | Blackberry Limited | Power supply management for portable electronic devices |
| US10085513B2 (en) * | 2014-08-27 | 2018-10-02 | Nike, Inc. | Article of footwear with soil-shedding performance |
| CN105970663A (zh) * | 2016-03-08 | 2016-09-28 | 安徽安利材料科技股份有限公司 | 一种高耐水解和高耐紫外光照老化自去污聚氨酯合成革的制造方法 |
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2017
- 2017-07-04 JP JP2019500318A patent/JP2019523043A/ja active Pending
- 2017-07-04 WO PCT/EP2017/066581 patent/WO2018007359A1/fr not_active Ceased
- 2017-07-04 CN CN201780042427.XA patent/CN109476810A/zh active Pending
- 2017-07-04 US US16/315,944 patent/US20200221825A1/en not_active Abandoned
- 2017-07-04 EP EP17742658.2A patent/EP3481882A1/fr not_active Withdrawn
- 2017-07-04 KR KR1020197000011A patent/KR20190024951A/ko not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| CN109476810A (zh) | 2019-03-15 |
| US20200221825A1 (en) | 2020-07-16 |
| KR20190024951A (ko) | 2019-03-08 |
| JP2019523043A (ja) | 2019-08-22 |
| WO2018007359A1 (fr) | 2018-01-11 |
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