ES2340756B1 - Compuesto para la fabricacion de una marca al agua en un material laminar textil y composicion, material, procedimiento y uso correspondientes. - Google Patents
Compuesto para la fabricacion de una marca al agua en un material laminar textil y composicion, material, procedimiento y uso correspondientes. Download PDFInfo
- Publication number
- ES2340756B1 ES2340756B1 ES201030052A ES201030052A ES2340756B1 ES 2340756 B1 ES2340756 B1 ES 2340756B1 ES 201030052 A ES201030052 A ES 201030052A ES 201030052 A ES201030052 A ES 201030052A ES 2340756 B1 ES2340756 B1 ES 2340756B1
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- compound
- textile
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- 239000000463 material Substances 0.000 title claims abstract description 71
- 239000004753 textile Substances 0.000 title claims abstract description 60
- 239000000203 mixture Substances 0.000 title claims abstract description 27
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 15
- 238000000034 method Methods 0.000 title claims abstract description 15
- 239000002131 composite material Substances 0.000 title claims 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 73
- -1 hexamethylene, trimethylhexamethylene Chemical group 0.000 claims abstract description 40
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 19
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims abstract description 9
- 239000008096 xylene Substances 0.000 claims abstract description 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 5
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 5
- 125000004955 1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C1([H])[*:2] 0.000 claims abstract description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 3
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical group CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
- XMGMFRIEKMMMSU-UHFFFAOYSA-N phenylmethylbenzene Chemical group C=1C=CC=CC=1[C]C1=CC=CC=C1 XMGMFRIEKMMMSU-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000006839 xylylene group Chemical group 0.000 claims abstract description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 55
- 229920000728 polyester Polymers 0.000 claims description 18
- 239000002904 solvent Substances 0.000 claims description 13
- 238000005406 washing Methods 0.000 claims description 12
- 238000004132 cross linking Methods 0.000 claims description 9
- 239000007983 Tris buffer Substances 0.000 claims description 8
- 239000003086 colorant Substances 0.000 claims description 8
- 238000007639 printing Methods 0.000 claims description 8
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims description 8
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 7
- 229920002972 Acrylic fiber Polymers 0.000 claims description 6
- 229920003043 Cellulose fiber Polymers 0.000 claims description 6
- 229920000742 Cotton Polymers 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 229920002647 polyamide Polymers 0.000 claims description 6
- 239000004814 polyurethane Substances 0.000 claims description 6
- 229920002635 polyurethane Polymers 0.000 claims description 6
- 239000004627 regenerated cellulose Substances 0.000 claims description 6
- 210000002268 wool Anatomy 0.000 claims description 6
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 4
- WUFHQGLVNNOXMP-UHFFFAOYSA-N n-(triethoxysilylmethyl)cyclohexanamine Chemical compound CCO[Si](OCC)(OCC)CNC1CCCCC1 WUFHQGLVNNOXMP-UHFFFAOYSA-N 0.000 claims description 4
- REODOQPOCJZARG-UHFFFAOYSA-N n-[[diethoxy(methyl)silyl]methyl]cyclohexanamine Chemical compound CCO[Si](C)(OCC)CNC1CCCCC1 REODOQPOCJZARG-UHFFFAOYSA-N 0.000 claims description 4
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical compound O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 claims description 3
- 238000005470 impregnation Methods 0.000 claims description 3
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000003944 tolyl group Chemical group 0.000 claims description 2
- 239000000047 product Substances 0.000 description 33
- 239000007787 solid Substances 0.000 description 24
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical group [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 15
- 229910000077 silane Inorganic materials 0.000 description 15
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 11
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 10
- 239000012467 final product Substances 0.000 description 10
- 239000012299 nitrogen atmosphere Substances 0.000 description 10
- 239000004744 fabric Substances 0.000 description 8
- 239000013638 trimer Substances 0.000 description 8
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 4
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 4
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 4
- 238000013508 migration Methods 0.000 description 4
- 230000005012 migration Effects 0.000 description 4
- 239000005058 Isophorone diisocyanate Substances 0.000 description 3
- 229920004482 WACKER® Polymers 0.000 description 3
- 239000001045 blue dye Substances 0.000 description 3
- 125000005442 diisocyanate group Chemical group 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000012948 isocyanate Substances 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 2
- QKOWXXDOHMJOMQ-UHFFFAOYSA-N 1,3,5-tris(6-isocyanatohexyl)biuret Chemical compound O=C=NCCCCCCNC(=O)N(CCCCCCN=C=O)C(=O)NCCCCCCN=C=O QKOWXXDOHMJOMQ-UHFFFAOYSA-N 0.000 description 2
- ZIZJPRKHEXCVLL-UHFFFAOYSA-N 1,3-bis(6-isocyanatohexyl)-1,3-diazetidine-2,4-dione Chemical compound O=C=NCCCCCCN1C(=O)N(CCCCCCN=C=O)C1=O ZIZJPRKHEXCVLL-UHFFFAOYSA-N 0.000 description 2
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 2
- XMVBHZBLHNOQON-UHFFFAOYSA-N 2-butyl-1-octanol Chemical compound CCCCCCC(CO)CCCC XMVBHZBLHNOQON-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 238000004873 anchoring Methods 0.000 description 2
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000539 dimer Substances 0.000 description 2
- 238000007647 flexography Methods 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 239000000576 food coloring agent Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000001043 yellow dye Substances 0.000 description 2
- 238000004383 yellowing Methods 0.000 description 2
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- YXRKNIZYMIXSAD-UHFFFAOYSA-N 1,6-diisocyanatohexane Chemical compound O=C=NCCCCCCN=C=O.O=C=NCCCCCCN=C=O.O=C=NCCCCCCN=C=O YXRKNIZYMIXSAD-UHFFFAOYSA-N 0.000 description 1
- QUTGXAIWZAMYEM-UHFFFAOYSA-N 2-cyclopentyloxyethanamine Chemical compound NCCOC1CCCC1 QUTGXAIWZAMYEM-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical class C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- IIGAAOXXRKTFAM-UHFFFAOYSA-N N=C=O.N=C=O.CC1=C(C)C(C)=C(C)C(C)=C1C Chemical compound N=C=O.N=C=O.CC1=C(C)C(C)=C(C)C(C)=C1C IIGAAOXXRKTFAM-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical group O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 239000001044 red dye Substances 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- SCPYDCQAZCOKTP-UHFFFAOYSA-N silanol Chemical compound [SiH3]O SCPYDCQAZCOKTP-UHFFFAOYSA-N 0.000 description 1
- 125000005372 silanol group Chemical group 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000001060 yellow colorant Substances 0.000 description 1
Classifications
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- 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
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- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/288—Compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/289—Compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
-
- 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
-
- 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
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- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/2815—Monohydroxy compounds
- C08G18/282—Alkanols, cycloalkanols or arylalkanols including terpenealcohols
-
- 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
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/2815—Monohydroxy compounds
- C08G18/282—Alkanols, cycloalkanols or arylalkanols including terpenealcohols
- C08G18/2825—Alkanols, cycloalkanols or arylalkanols including terpenealcohols having at least 6 carbon 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
- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/8064—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with monohydroxy compounds
-
- 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
- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/8083—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with compounds containing at least one heteroatom other than oxygen or nitrogen
- C08G18/809—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with compounds containing at least one heteroatom other than oxygen or nitrogen containing silicon
-
- 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
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- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/8096—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with two or more compounds having only one group containing active hydrogen
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L75/00—Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
- C08L75/04—Polyurethanes
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06Q—DECORATING TEXTILES
- D06Q1/00—Decorating textiles
- D06Q1/02—Producing patterns by locally destroying or modifying the fibres of a web by chemical actions, e.g. making translucent
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M3/00—Printing processes to produce particular kinds of printed work, e.g. patterns
- B41M3/10—Watermarks
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- 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
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
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- 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
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- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
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- Y10T428/2481—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] including layer of mechanically interengaged strands, strand-portions or strand-like strips
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Abstract
Description
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- a)
- X es hexametilen, trimetilhexametilen, isoforon, diciclohexilmetil, tetrametilxililen, tetrametilen xilen, xililen, trimetilhexametilen, 4,4'difenilmetilen hidrogenado, 1,12 dodecilen, 1,5-2-metilpentilen, 1,4-butilen, 1,4 ciclohexilen, o un compuesto de fórmula
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- \quad
- usualmente denominado 1,3-diazetidin-2,4-diona 1,3-bis(6-hexil) o 2,4-dioxo-1,3-diazetidin-1,3-bis(hexametilen)
- \quad
- o un compuesto de fórmula
- \quad
- usualmente denominado 1,3,5-triazin-2,4,6(1H,3H,5H)-triona 1,3,5-tris(6-hexil) o (2,4,6-trioxotriazin-1,3,5(2H,4H,6H)-triil) tris(hexametilen)
- \quad
- o un compuesto de fórmula
- \quad
- usualmente denominado diamida imidodicarbonica N,N',2-tris(6-hexil),
- \quad
- o un compuesto de fórmula
- b)
- R_{1} es un radical C1-C12 alquilo alifático lineal, o un radical C3-C18 alquilo alifático ramificado
- c)
- R_{2} es un radical de fórmula
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- \quad
- donde
- c1)
- R_{4} es metoxi o etoxi,
- c2)
- R_{5} es H, metoxi, etoxi, metilo o etilo,
- c3)
- R_{6} es H, metoxi, etoxi, metilo o etilo,
- c4)
- R_{7} es ciclohexil, fenilo o C3-C6 alquilo alifático,
- d)
- R_{3} es un radical C1-C12 alquilo alifático lineal, o un radical C3-C18 alquilo alifático ramificado, y
- e)
- n es 0 ó 1.
fluidos.
tejido.
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AG.
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\newpage
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Claims (28)
4H,6H)-triil)tris(hexametilen)
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agua.
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Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES201030052A ES2340756B1 (es) | 2010-01-18 | 2010-01-18 | Compuesto para la fabricacion de una marca al agua en un material laminar textil y composicion, material, procedimiento y uso correspondientes. |
US13/522,518 US8815001B2 (en) | 2010-01-18 | 2011-01-17 | Compound for manufacturing watermark in a textile sheet material and the corresponding composition, material, method and use |
PCT/ES2011/070025 WO2011086224A2 (es) | 2010-01-18 | 2011-01-17 | Compuesto para la fabricación de una marca al agua en un material laminar textil y composición, material, procedimiento y uso correspondientes |
EP11715712.3A EP2527384B1 (en) | 2010-01-18 | 2011-01-17 | A compound for making a watermark on a laminated textile material and corresponding composition, material, method and use |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES201030052A ES2340756B1 (es) | 2010-01-18 | 2010-01-18 | Compuesto para la fabricacion de una marca al agua en un material laminar textil y composicion, material, procedimiento y uso correspondientes. |
Publications (2)
Publication Number | Publication Date |
---|---|
ES2340756A1 ES2340756A1 (es) | 2010-06-08 |
ES2340756B1 true ES2340756B1 (es) | 2011-07-21 |
Family
ID=42194737
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES201030052A Expired - Fee Related ES2340756B1 (es) | 2010-01-18 | 2010-01-18 | Compuesto para la fabricacion de una marca al agua en un material laminar textil y composicion, material, procedimiento y uso correspondientes. |
Country Status (4)
Country | Link |
---|---|
US (1) | US8815001B2 (es) |
EP (1) | EP2527384B1 (es) |
ES (1) | ES2340756B1 (es) |
WO (1) | WO2011086224A2 (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2386179B1 (es) * | 2012-06-13 | 2013-05-08 | Antonio Oliva Gurgui | Compuestos derivados de uretanos y oligouretanos y procedimientos de fabricación de marcas al agua mediante la técnica de impresión offset y usos correspondientes |
US9139753B2 (en) * | 2013-03-14 | 2015-09-22 | The United States Of America, As Represented By The Secretary Of The Navy | Single-component moisture-curable coatings based on N-substituted urea polymers with extended chains and terminal alkoxysilanes |
WO2015178965A1 (en) * | 2014-05-19 | 2015-11-26 | Avery Dennison Retail Information Services Llc | Composite image heat transfer with scannable mark |
ES2644165B1 (es) * | 2016-05-25 | 2018-09-11 | Identity Mark S.L. | Compuesto para la fabricación de una marca al agua en un material laminar textil y una composición, material textil, procedimientos y usos correspondientes |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3903052A (en) * | 1972-09-06 | 1975-09-02 | Bayer Ag | Polymers containing alkoxysilyl-substituted biuret groups and processes for their preparation |
US4048207A (en) * | 1975-10-14 | 1977-09-13 | E. I. Du Pont De Nemours And Company | Polymeric materials with silane end groups |
US4508889A (en) * | 1984-07-19 | 1985-04-02 | Desoto, Inc. | Preparation of isocyanate-terminated polyurethanes containing amino silanes |
JPS62250021A (ja) * | 1986-04-22 | 1987-10-30 | Natoko Paint Kk | 塗料組成物 |
WO1990010026A1 (de) * | 1989-02-24 | 1990-09-07 | Henkel Kommanditgesellschaft Auf Aktien | Alkoxysilangruppenterminierte polyurethane zur ausrüstung von polyesterhaltigen textilfasermaterialien |
JP2006111811A (ja) * | 2004-10-18 | 2006-04-27 | Yokohama Rubber Co Ltd:The | 2液硬化型ポリウレタン樹脂組成物 |
WO2008009388A1 (en) * | 2006-07-17 | 2008-01-24 | Oliva Gurgui Antonia | Polyurethane derivates and corresponding uses and methods for producing watermarks |
WO2008135273A1 (en) * | 2007-05-07 | 2008-11-13 | Antonio Oliva Gurgui | Urethane and oligourethane derivatives and corresponding uses and methods for producing water marks using the offset printing technique |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE637578A (es) * | 1962-09-19 | |||
US3676478A (en) * | 1968-12-04 | 1972-07-11 | Bayer Ag | Silyl-substituted urea derivatives |
DE2044838A1 (de) * | 1970-09-10 | 1972-03-16 | Bayer | Vernetzte Polyurethanformkörper |
GB2282611B (en) * | 1993-09-27 | 1997-01-29 | Portals Ltd | Improvement in security features for paper |
DE19727029B4 (de) | 1997-06-25 | 2006-11-09 | Henkel Kgaa | Einkomponentige Reaktivsystem-Zusammensetzung, Verfahren zu ihrer Herstellung und ihre Verwendung |
DE19855999A1 (de) | 1998-12-04 | 2000-06-15 | Bayer Ag | Alkoxysilanhaltige Lackzubereitung |
FR2864537B1 (fr) * | 2003-12-24 | 2006-02-17 | Rhodia Chimie Sa | Synthese de biurets et d'isocyanates a fonctions alcoxysilanes, formulations en contenant et leurs applications |
US8378037B2 (en) * | 2007-12-26 | 2013-02-19 | Momentive Performance Materials Inc. | Moisture-curable silylated polyurea and adhesive, sealant and coating compositions containing same |
AT508458B1 (de) | 2009-06-30 | 2011-06-15 | Banny Reiter Ulrike | Vorrichtung und verfahren zum reinigen von abwasserleitungen von unterdrucktoilettenanlagen |
-
2010
- 2010-01-18 ES ES201030052A patent/ES2340756B1/es not_active Expired - Fee Related
-
2011
- 2011-01-17 WO PCT/ES2011/070025 patent/WO2011086224A2/es active Application Filing
- 2011-01-17 EP EP11715712.3A patent/EP2527384B1/en not_active Not-in-force
- 2011-01-17 US US13/522,518 patent/US8815001B2/en not_active Expired - Fee Related
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3903052A (en) * | 1972-09-06 | 1975-09-02 | Bayer Ag | Polymers containing alkoxysilyl-substituted biuret groups and processes for their preparation |
US4048207A (en) * | 1975-10-14 | 1977-09-13 | E. I. Du Pont De Nemours And Company | Polymeric materials with silane end groups |
US4508889A (en) * | 1984-07-19 | 1985-04-02 | Desoto, Inc. | Preparation of isocyanate-terminated polyurethanes containing amino silanes |
JPS62250021A (ja) * | 1986-04-22 | 1987-10-30 | Natoko Paint Kk | 塗料組成物 |
WO1990010026A1 (de) * | 1989-02-24 | 1990-09-07 | Henkel Kommanditgesellschaft Auf Aktien | Alkoxysilangruppenterminierte polyurethane zur ausrüstung von polyesterhaltigen textilfasermaterialien |
JP2006111811A (ja) * | 2004-10-18 | 2006-04-27 | Yokohama Rubber Co Ltd:The | 2液硬化型ポリウレタン樹脂組成物 |
WO2008009388A1 (en) * | 2006-07-17 | 2008-01-24 | Oliva Gurgui Antonia | Polyurethane derivates and corresponding uses and methods for producing watermarks |
WO2008135273A1 (en) * | 2007-05-07 | 2008-11-13 | Antonio Oliva Gurgui | Urethane and oligourethane derivatives and corresponding uses and methods for producing water marks using the offset printing technique |
Non-Patent Citations (1)
Title |
---|
H. NI et al., "{}Preparation and characterization of alcoxysilane functionalized isocyanurates"{}, Polymer, 2000, vol. 41, páginas 57-71, ver apartado 2.4 y compuestos 6 y 7. * |
Also Published As
Publication number | Publication date |
---|---|
ES2340756A1 (es) | 2010-06-08 |
US8815001B2 (en) | 2014-08-26 |
EP2527384A2 (en) | 2012-11-28 |
WO2011086224A3 (es) | 2012-06-14 |
EP2527384B1 (en) | 2014-10-08 |
WO2011086224A2 (es) | 2011-07-21 |
US20120295079A1 (en) | 2012-11-22 |
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