WO2006087348A1 - Polyurethandispersion für die verbundfolienkaschierung - Google Patents
Polyurethandispersion für die verbundfolienkaschierung Download PDFInfo
- Publication number
- WO2006087348A1 WO2006087348A1 PCT/EP2006/050968 EP2006050968W WO2006087348A1 WO 2006087348 A1 WO2006087348 A1 WO 2006087348A1 EP 2006050968 W EP2006050968 W EP 2006050968W WO 2006087348 A1 WO2006087348 A1 WO 2006087348A1
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- WO
- WIPO (PCT)
- Prior art keywords
- compounds
- mol
- dispersion according
- polyurethane
- ionic group
- Prior art date
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- 239000002131 composite material Substances 0.000 title claims description 18
- 238000003475 lamination Methods 0.000 title claims description 5
- 229920003009 polyurethane dispersion Polymers 0.000 title description 18
- 150000001875 compounds Chemical class 0.000 claims abstract description 34
- 125000003010 ionic group Chemical group 0.000 claims abstract description 19
- 229920002635 polyurethane Polymers 0.000 claims abstract description 19
- 239000004814 polyurethane Substances 0.000 claims abstract description 19
- 150000001298 alcohols Chemical class 0.000 claims abstract description 14
- 239000006185 dispersion Substances 0.000 claims abstract description 14
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims abstract description 13
- 239000003054 catalyst Substances 0.000 claims abstract description 9
- 238000006243 chemical reaction Methods 0.000 claims abstract description 9
- 125000005442 diisocyanate group Chemical group 0.000 claims abstract description 9
- 229910021529 ammonia Inorganic materials 0.000 claims abstract description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000000853 adhesive Substances 0.000 claims description 11
- 230000001070 adhesive effect Effects 0.000 claims description 11
- 239000012939 laminating adhesive Substances 0.000 claims description 11
- 229920000098 polyolefin Polymers 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 229920006267 polyester film Polymers 0.000 claims description 5
- 239000011140 metalized polyester Substances 0.000 claims description 4
- 239000000470 constituent Substances 0.000 claims description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- MMCOUVMKNAHQOY-UHFFFAOYSA-N carbonoperoxoic acid Chemical class OOC(O)=O MMCOUVMKNAHQOY-UHFFFAOYSA-N 0.000 claims description 2
- 229920000570 polyether Polymers 0.000 claims description 2
- 239000003431 cross linking reagent Substances 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 19
- -1 polyethylene Polymers 0.000 description 16
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 239000012948 isocyanate Substances 0.000 description 9
- 239000000203 mixture Substances 0.000 description 9
- 150000002596 lactones Chemical class 0.000 description 7
- 239000005026 oriented polypropylene Substances 0.000 description 7
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 5
- 150000002513 isocyanates Chemical class 0.000 description 5
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 229920005906 polyester polyol Polymers 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 4
- PTBDIHRZYDMNKB-UHFFFAOYSA-N 2,2-Bis(hydroxymethyl)propionic acid Chemical compound OCC(C)(CO)C(O)=O PTBDIHRZYDMNKB-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 229920006378 biaxially oriented polypropylene Polymers 0.000 description 4
- 239000011127 biaxially oriented polypropylene Substances 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 4
- 229940117969 neopentyl glycol Drugs 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229920001451 polypropylene glycol Polymers 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000004146 Propane-1,2-diol Substances 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical class O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 229960004063 propylene glycol Drugs 0.000 description 3
- 235000013772 propylene glycol Nutrition 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 3
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 3
- OZCRKDNRAAKDAN-HNQUOIGGSA-N (e)-but-1-ene-1,4-diol Chemical compound OCC\C=C\O OZCRKDNRAAKDAN-HNQUOIGGSA-N 0.000 description 2
- NNOZGCICXAYKLW-UHFFFAOYSA-N 1,2-bis(2-isocyanatopropan-2-yl)benzene Chemical compound O=C=NC(C)(C)C1=CC=CC=C1C(C)(C)N=C=O NNOZGCICXAYKLW-UHFFFAOYSA-N 0.000 description 2
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 2
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 239000004358 Butane-1, 3-diol Substances 0.000 description 2
- 239000004971 Cross linker Substances 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- 239000005058 Isophorone diisocyanate Substances 0.000 description 2
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical class OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 2
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 2
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 2
- 238000007259 addition reaction Methods 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- 235000019437 butane-1,3-diol Nutrition 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000012975 dibutyltin dilaurate Substances 0.000 description 2
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- GHLKSLMMWAKNBM-UHFFFAOYSA-N dodecane-1,12-diol Chemical compound OCCCCCCCCCCCCO GHLKSLMMWAKNBM-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 2
- SAMYCKUDTNLASP-UHFFFAOYSA-N hexane-2,2-diol Chemical class CCCCC(C)(O)O SAMYCKUDTNLASP-UHFFFAOYSA-N 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 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 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920001748 polybutylene Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920000915 polyvinyl chloride Polymers 0.000 description 2
- 239000000565 sealant Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 2
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 2
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 1
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
- GFNDFCFPJQPVQL-UHFFFAOYSA-N 1,12-diisocyanatododecane Chemical compound O=C=NCCCCCCCCCCCCN=C=O GFNDFCFPJQPVQL-UHFFFAOYSA-N 0.000 description 1
- OHLKMGYGBHFODF-UHFFFAOYSA-N 1,4-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=C(CN=C=O)C=C1 OHLKMGYGBHFODF-UHFFFAOYSA-N 0.000 description 1
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 description 1
- OVBFMUAFNIIQAL-UHFFFAOYSA-N 1,4-diisocyanatobutane Chemical compound O=C=NCCCCN=C=O OVBFMUAFNIIQAL-UHFFFAOYSA-N 0.000 description 1
- CDMDQYCEEKCBGR-UHFFFAOYSA-N 1,4-diisocyanatocyclohexane Chemical compound O=C=NC1CCC(N=C=O)CC1 CDMDQYCEEKCBGR-UHFFFAOYSA-N 0.000 description 1
- LFSYUSUFCBOHGU-UHFFFAOYSA-N 1-isocyanato-2-[(4-isocyanatophenyl)methyl]benzene Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=CC=C1N=C=O LFSYUSUFCBOHGU-UHFFFAOYSA-N 0.000 description 1
- LYDHLGJJJAWBDY-UHFFFAOYSA-N 1-isocyanato-4-[2-(4-isocyanatocyclohexyl)propan-2-yl]cyclohexane Chemical compound C1CC(N=C=O)CCC1C(C)(C)C1CCC(N=C=O)CC1 LYDHLGJJJAWBDY-UHFFFAOYSA-N 0.000 description 1
- WMRCTEPOPAZMMN-UHFFFAOYSA-N 2-undecylpropanedioic acid Chemical compound CCCCCCCCCCCC(C(O)=O)C(O)=O WMRCTEPOPAZMMN-UHFFFAOYSA-N 0.000 description 1
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 1
- YTALMPUNNICJOM-UHFFFAOYSA-N 5-ethyl-3-methyloxolan-2-one Chemical compound CCC1CC(C)C(=O)O1 YTALMPUNNICJOM-UHFFFAOYSA-N 0.000 description 1
- KNDQHSIWLOJIGP-UHFFFAOYSA-N 826-62-0 Chemical compound C1C2C3C(=O)OC(=O)C3C1C=C2 KNDQHSIWLOJIGP-UHFFFAOYSA-N 0.000 description 1
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- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 1
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- 125000000129 anionic group Chemical group 0.000 description 1
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- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
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- VANNPISTIUFMLH-UHFFFAOYSA-N glutaric anhydride Chemical compound O=C1CCCC(=O)O1 VANNPISTIUFMLH-UHFFFAOYSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
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- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 229960000380 propiolactone Drugs 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- AUHHYELHRWCWEZ-UHFFFAOYSA-N tetrachlorophthalic anhydride Chemical compound ClC1=C(Cl)C(Cl)=C2C(=O)OC(=O)C2=C1Cl AUHHYELHRWCWEZ-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/06—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material
- B32B27/08—Layered products comprising a layer of synthetic resin as the main or only constituent of a layer, which is next to another layer of the same or of a different material of synthetic resin
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/32—Layered products comprising a layer of synthetic resin comprising polyolefins
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/36—Layered products comprising a layer of synthetic resin comprising polyesters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B7/00—Layered products characterised by the relation between layers; Layered products characterised by the relative orientation of features between layers, or by the relative values of a measurable parameter between layers, i.e. products comprising layers having different physical, chemical or physicochemical properties; Layered products characterised by the interconnection of layers
- B32B7/04—Interconnection of layers
- B32B7/12—Interconnection of layers using interposed adhesives or interposed materials with bonding properties
-
- 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
- C08G18/0838—Manufacture of polymers in the presence of non-reactive compounds
- C08G18/0842—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents
- C08G18/0861—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents in the presence of a dispersing phase for the polymers or a phase dispersed in the polymers
- C08G18/0866—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents in the presence of a dispersing phase for the polymers or a phase dispersed in the polymers the dispersing or dispersed phase being an aqueous medium
-
- 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
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6666—Compounds of group C08G18/48 or C08G18/52
- C08G18/6692—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/34
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J175/00—Adhesives based on polyureas or polyurethanes; Adhesives based on derivatives of such polymers
- C09J175/04—Polyurethanes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2250/00—Layers arrangement
- B32B2250/02—2 layers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2250/00—Layers arrangement
- B32B2250/24—All layers being polymeric
- B32B2250/242—All polymers belonging to those covered by group B32B27/32
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/10—Coating on the layer surface on synthetic resin layer or on natural or synthetic rubber layer
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/20—Inorganic coating
- B32B2255/205—Metallic coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2255/00—Coating on the layer surface
- B32B2255/26—Polymeric coating
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2307/00—Properties of the layers or laminate
- B32B2307/70—Other properties
- B32B2307/714—Inert, i.e. inert to chemical degradation, corrosion
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2553/00—Packaging equipment or accessories not otherwise provided for
-
- 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
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31551—Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
- Y10T428/31573—Next to addition polymer of ethylenically unsaturated monomer
- Y10T428/31587—Hydrocarbon polymer [polyethylene, polybutadiene, etc.]
Definitions
- the invention relates to an aqueous dispersion containing a polyurethane composed of
- organic diisocyanates b) dihydroxy compounds having a molecular weight of 500 to 5000 g / mol which contain no ionic or ionic group convertible group c) monohydric to trihydric alcohols which additionally contain an ionic group d) optionally further from a) to c) different connections,
- the polyurethane contains less than 0.6% by weight of urea groups (calculated with a molecular weight of 56 g / mol),
- the ionic group of c) is at least partially neutralized with ammonia
- reaction of the compounds a), b), c) and d) is not carried out in the presence of a catalyst with a metal-carbon compound.
- the invention relates to the use of the dispersion as a laminating adhesive, in particular as a one-component (1 K) Kaschierklebstoff.
- a laminating adhesive in particular as a one-component (1 K) Kaschierklebstoff.
- 1 K laminating adhesives in contrast to 2K laminating adhesives, no crosslinker is added.
- Laminating adhesives are e.g. used for the production of composite film (composite film lamination).
- the bonding or lamination of foils made of different materials combines the properties of these materials.
- the aim of such a measure may be to achieve special decorative effects, or to bring about technical effects such as protection of an imprint, production of heat-resistant film composites, inhibition of vapor diffusion, heat-sealability, reliable prevention of porosity or resistance to aggressive goods.
- the film materials which are essentially used are polyethylene, polypropylene, in particular biaxially oriented polypropylene, polyamide, polyester, PVC, cellulose acetate, cellophane and metals such as tin or aluminum.
- the strength of the composite films achieved with the previously described 1K polyurethane dispersions is not yet sufficient, in particular in the case of film composites made from biaxially oriented polypropylene (OPP) and film composites made from OPP films and metallized polyester films.
- OPP biaxially oriented polypropylene
- the object of the present invention was therefore polyurethane dispersions which, when used as a laminating adhesive, bring about a higher strength of the film composites.
- the polyurethane is made up of
- organic diisocyanates b) dihydroxy compounds having a molecular weight of 500 to 5000 g / mol which do not contain an ionic or ionic group convertible group c) monohydric to trihydric alcohols which additionally contain an ionic group and d) optionally further of (a) to c) different compounds.
- Diisocyanates a) include in particular diisocyanates X (NCO) 2, where X is an aliphatic hydrocarbon radical having 4 to 15 carbon atoms, a cycloaliphatic or aromatic hydrocarbon radical having 6 to 15 carbon atoms or an araliphatic hydrocarbon radical having 7 to 15 carbon atoms.
- diisocyanates examples include tetramethylene diisocyanate, hexamethylene diisocyanate, dodecamethylene diisocyanate, 1,4-diisocyanatocyclohexane, 1-isocyanato-S. ⁇ . ⁇ -trimethyl-S-isocyanatomethylcyclohexane (IPDI), 2,2-bis (4-isocyanatocyclohexyl) propane , Trimethylhexandiisocyanat, 1, 4-diisocyanatobenzene, 2,4-diisocyanatotoluene, 2,6-diisocyanatotoluene, 4,4'-diisocyanato-diphenylmethane, 2,4'-diisocyanato-diphenylmethane, p-xylylene diisocyanate, tetramethylxylylene diisocyanate (TMXDI) 1, the isomers of bis (4-isocyanate
- Such diisocyanates are available commercially.
- mixtures of these isocyanates especially the mixtures of the respective structural isomers of diisocyanatotoluene and diisocyanato-diphenylmethane are of importance, in particular, the mixture of 80 mol% of 2,4-diisocyanatotoluene and 20 mol% of 2,6-diisocyanatotoluene is suitable.
- mixtures of aromatic isocyanates such as 2,4-diisocyanatotoluene and / or 2,6-diisocyanatotoluene with aliphatic or cycloaliphatic isocyanates such as hexamethylene diisocyanate or IPDI are particularly advantageous, the preferred mixing ratio of the aliphatic to aromatic isocyanates 4: 1 to 1: 4.
- the dihydroxy compounds b) may be polyester polyols, the z. B. from Ullmann's Encyclopedia of Industrial Chemistry, 4th Edition, Volume 19, pp 62 to 65 are known. Preference is given to using polyesterpolyols which are obtained by reacting dihydric alcohols with dibasic carboxylic acids. Instead of the free polycarboxylic acids, it is also possible to use the corresponding polycarboxylic acid anhydrides or corresponding polycarboxylic acid esters of lower alcohols or mixtures thereof to prepare the polyesterpolyols.
- the polycarboxylic acids may be aliphatic, cycloaliphatic, araliphatic, aromatic or heterocyclic and optionally, for. B.
- dihydric alcohols come z.
- ethylene glycol propane-1, 2-diol, propane-1,3-diol, butane-1,3-diol, butene-1, 4-diol, butyne-1, 4-dioI, pentane-1,5- diol, neopentyl glycol, bis (hydroxymethyl) cyclohexanes, such as 1,4-bis (hydroxymethyl) cyclohexane, 2-methylpropane-1,3-diol, methylpentanediols, furthermore diethylene glycol, triethylene glycol, tetraethylene glycol, polyethylene glycol, dipropylene glycol, Polypropylene glycol, dibutylene glycol and polybutylene glycols into consideration.
- Alcohols of the general formula HO- (CH 2) x -OH are preferred, where x is a number from 1 to 20, preferably an even number from 2 to 20.
- examples of these are ethylene glycol, butane-1,4-diol, hexane-1,6-diol, octane-1, 8-diol and dodecane-1, 12-diol. Further preferred is neopentyl glycol.
- polycarbonate diols as they are, for. B. can be obtained by reacting phosgene with an excess of the mentioned as synthesis components for the polyester polyols low molecular weight alcohols into consideration.
- polyester-based lactone-based lubricants which are homopolymers or copolymers of lactones, preferably addition products of lactones having terminal hydroxyl groups. nete difunctional starter molecules.
- Preferred lactones are those which are derived from compounds of the general formula HO- (CH 2 ) Z-COOH, where z is a number from 1 to 20 and an H atom of a methylene unit is also denoted by a C 1 to C 4 Alkyl may be substituted. Examples are ⁇ -caprolactone, ⁇ -propiolactone, ⁇ -butyrolactone and / or methyl- ⁇ -caprolactone and mixtures thereof. Suitable starter components are for.
- polyester polyols low molecular weight dihydric alcohols.
- the corresponding polymers of ⁇ -caprolactone are particularly preferred.
- Lower polyester diols or polyether diols can also be used as starters for the preparation of the lactone polymers.
- the polymers of lactones it is also possible to use the corresponding, chemically equivalent polycondensates of the hydroxycarboxylic acids corresponding to the lactones.
- Polyetherdiols are in particular by polymerization of ethylene oxide, propylene oxide, butylene oxide, tetrahydrofuran, styrene oxide or epichlorohydrin with itself, z. B. in the presence of BF3 or by addition of these compounds, optionally in admixture or in succession, to starting components with reactive hydrogen atoms, such as alcohols or amines, for.
- reactive hydrogen atoms such as alcohols or amines, for.
- water ethylene glycol, propane-1, 2-diol, propane-1,3-diol, 2,2-bis (4-hydroxyphenyl) propane or aniline available.
- Preferred compounds b) are polyetherols.
- at least 50% by weight, particularly preferably at least 85% by weight, very particularly preferably at least 95% by weight or at 100% by weight of the compounds b) are polyetherols.
- the molecular weight of compounds b) is preferably from 1000 to 3000 g / mol. It is the number average molecular weight, determined by the number of end groups (OH number).
- the monohydric to trihydric alcohols c) contain in particular anionic groups such as the sulfonate, the carboxylate and the phosphate group.
- anionic group is intended to include those groups that can be converted to ionic groups.
- carboxylic acid, sulfonic acid or phosphoric acid groups are also considered to be ionic groups.
- Aliphatic, cycloaliphatic, ara-aliphatic or aromatic carboxylic acids and sulfonic acids which carry at least one alcoholic hydroxyl group are usually suitable.
- R 1 and R 2 is a C 1 to C 4 alkanediyl (unit) and R 3 is a C 1 to C 4 alkyl (unit) and, in particular, dimethylolpropionic acid (DMPA) is preferred.
- DMPA dimethylolpropionic acid
- Isocyanate compounds having more than two isocyanate groups e.g. are obtainable by biuret or isocyanurate formation from the above diisocyanates.
- Alcohols of the general formula HO- (CH 2 ) X-OH are preferred, where x is a number from 1 to 20, preferably an even number from 2 to 20.
- x is a number from 1 to 20, preferably an even number from 2 to 20.
- examples of these are ethylene glycol, butane-1, 4-diol, hexane-1,6-diol, octane-1, 8-diol and dodecane-1, 12-diol.
- Further preferred is neopentyl glycol.
- compounds d) having only one isocyanate group or an isocyanate-reactive group, in particular monoalcohols are usually used to regulate the molecular weight.
- the polyurethane is at least 50 wt .-%, more preferably at least 80 wt .-%, most preferably at least 90 wt .-% of compounds a) and b).
- the proportion of components c) in the total amount of components (a), (b), (c), (d) is generally such that the molar amount of the ionic groups, based on the weight of all monomers (a) to ( d), 30 to 1000, preferably 50 to 800 and particularly preferably 80 to 600 mmol / kg of polyurethane.
- the content of compounds d) is preferably less than 10 wt .-%, more preferably less than 5 or 2 wt .-%, most preferably less than 1 wt .-%.
- the polyurethane consists exclusively of a), b) and c).
- the ionic group of c) is at least partially neutralized with ammonia
- reaction of the compounds a), b), c) and d) is not carried out in the presence of a catalyst having metal-carbon bonds.
- the content of urea groups is preferably less than 0.5, more preferably less than 0.4 wt .-%.
- the polyurethane is substantially free of urea groups.
- the ionic groups of c) are preferably at least 20 mole%, more preferably at least 30 mole%, most preferably at least 50 mole% neutralized with ammonia, i. they are present as the salt of Ammoniumkations.
- 20 to 80 mol%, particularly preferably 30 to 70 mol% of the ionic groups c) are neutralized with ammonia.
- Metal-organic compounds ie, compounds with a metal-carbon bond
- tin-organic compounds such as dibutyltin dilaurate
- catalysts are often used as catalysts in the reaction of isocyanate with hydroxyl groups.
- such compounds having a metal-carbon bond as catalyst are omitted in the reaction.
- metal-containing catalysts nor other catalysts are preferably used in the reaction of isocyanate compounds with compounds containing hydroxyl groups.
- A is the molar amount of isocyanate groups
- B is the sum of the molar amount of the hydroxyl groups and the molar amount of the functional groups which can react with isocyanates in an addition reaction
- the ratio A: B is as close as possible to 1: 1.
- the monomers (a) to (d) used usually carry on average 1.5 to 2.5, preferably 1.9 to 2.1, particularly preferably 2.0 isocyanate groups or functional groups which can react with isocyanates in an addition reaction ,
- the polyaddition of components (a) to (d) for the preparation of the polyurethane is preferably carried out at reaction temperatures of up to 18O 0 C, preferably up to 15O 0 C under atmospheric pressure or under autogenous pressure.
- the aqueous polyurethane dispersions obtained generally have a solids content of from 10 to 70, preferably from 15 to 50,% by weight.
- the polyurethanes in N, N-dimethylformamide (DMF, 21 0 C) usually have a K value of 20 to 60 on.
- the K value is a relative viscosity number, which is determined in analogy to DIN 53 726 at 25 °. It contains the flow rate of a 1% strength by weight solution of the polyurea rethans in DMF, relative to the flow rate of pure DMF and characterizes the average molecular weight of the polyurethane.
- the polyurethane dispersions can be used without further additives as an adhesive or sealant.
- the adhesives or sealants according to the invention contain the polyurethane dispersions and optionally further constituents.
- the adhesives may include pressure-sensitive adhesives, contact adhesives (double-sided adhesive application), foam adhesives (adhesive containing foaming agents) or laminating adhesives, e.g. B. also for automotive interior parts act.
- substrates to be bonded As substrates to be bonded z. As those of wood, metal, plastic, paper into consideration.
- the adhesives preferably contain no compounds which react with the polyurethane with crosslinking.
- the polyurethane dispersions according to the invention are accordingly preferably used as one-component (1 K) adhesives, in particular 1 K laminating adhesives.
- polyurethane dispersions are particularly suitable as an adhesive for the production of composite films, wherein, as already described above, different films are glued together for various purposes.
- the film materials which are essentially used are polyethylene, polypropylene, in particular biaxially oriented polypropylene (OPP), polyamide, polyester, PVC, cellulose acetate, cellulosic glass and metals such as tin and aluminum, in particular also metallized polymer films, e.g. As metallized polyolefin or polyester films.
- the polymer films in particular polyolefin films, may optionally be corona treated.
- the laminating adhesive is applied to at least one generally only one of the substrates to be bonded.
- the coated substrates are generally dried briefly and then pressed preferably at a temperature of 30 to 8O 0 C with each other or with uncoated substrates.
- the bond obtained, in particular the film composite obtained has a high bond strength at room temperature, as is generally achievable only in the case of two-component systems using a crosslinker.
- a particularly high strength is achieved in the bonding of polyolefin films, in particular OPP films with one another or in the bonding of polyolefin films, preferably OPP films with metallized polyester films.
- a mixture of 174.2 g (1.00 mol) of diisocyanatotoluene (80% 2,4-isomer, 20% 2,6-isomer), 800 g (0.40 mol) of polypropylene glycol of OH number 56, 80.3 g (0.60 mol) of dimethylolpropionic acid and 100 g of acetone was reacted at 95 ° C for five hours. It was then cooled to 30 0 C and determines the content of unreacted NCO groups to 0.06 wt.%. Thereafter, it was diluted with 800 g of acetone and then stirred successively 16.0 g (0.24 mol) of a 24 wt .-% aqueous ammonia solution and 1500 g of water. After distillation of the acetone, an approximately 40% strength by weight aqueous polyurethane dispersion was obtained.
- a mixture of 174.2 g (1.00 mol) of diisocyanatotoluene (80% 2,4-isomer, 20% 2,6-isomer), 800 g (0.40 mol) of polypropylene glycol of OH number 56, 80.3 g (0.60 mol) of dimethylolpropionic acid, 0.4 g of dibutyltin dilaurate and 100 g of acetone was reacted at 95.degree. C. for five hours. It was then cooled to 30 0 C and determines the content of unreacted NCO groups to 0.07 wt.%.
- the polyurethane dispersion was applied in an amount of 4 g / m 2 with a 0.2 mm roller blade.
- the coated films were dried with a hot air blower for about 2 minutes and pressed in a roller press at 70 0 C and 6.5 bar at a speed of 5 m / min with another film (with OPP film or metallized polyester film).
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Polyurethanes Or Polyureas (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Laminated Bodies (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/815,901 US20080145671A1 (en) | 2005-02-19 | 2006-02-15 | Polyurethane Dispersion for Composition Film Lamination |
JP2007555606A JP2008530329A (ja) | 2005-02-19 | 2006-02-15 | 複合シートを積層するためのポリウレタン分散液 |
PL06708294T PL1853640T3 (pl) | 2005-02-19 | 2006-02-15 | Dyspersja poliuretanowa do laminowania folii kompozytowych |
MX2007009191A MX2007009191A (es) | 2005-02-19 | 2006-02-15 | Dispersion de poliuretano para laminacion de pelicula compuesta. |
EP06708294.1A EP1853640B1 (de) | 2005-02-19 | 2006-02-15 | Polyurethandispersion für die verbundfolienkaschierung |
BRPI0607767A BRPI0607767B1 (pt) | 2005-02-19 | 2006-02-15 | dispersão aquosa, e, uso da mesma |
ES06708294.1T ES2534997T3 (es) | 2005-02-19 | 2006-02-15 | Dispersión de poliuretano para el contracolado de láminas compuestas |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE200510006235 DE102005006235A1 (de) | 2005-02-19 | 2005-02-19 | Polyurethandispersion für die Verbundfolienkaschierung |
DE102005006235.0 | 2005-02-19 |
Publications (1)
Publication Number | Publication Date |
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WO2006087348A1 true WO2006087348A1 (de) | 2006-08-24 |
Family
ID=36190426
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2006/050968 WO2006087348A1 (de) | 2005-02-19 | 2006-02-15 | Polyurethandispersion für die verbundfolienkaschierung |
Country Status (11)
Country | Link |
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US (1) | US20080145671A1 (de) |
EP (1) | EP1853640B1 (de) |
JP (1) | JP2008530329A (de) |
KR (1) | KR20070114169A (de) |
CN (1) | CN101120031A (de) |
BR (1) | BRPI0607767B1 (de) |
DE (1) | DE102005006235A1 (de) |
ES (1) | ES2534997T3 (de) |
MX (1) | MX2007009191A (de) |
PL (1) | PL1853640T3 (de) |
WO (1) | WO2006087348A1 (de) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10240071B2 (en) | 2014-12-05 | 2019-03-26 | Basf Se | Aqueous adhesive dispersion containing polyurethanes and ethoxylated fatty alcohols |
WO2021175676A1 (en) | 2020-03-02 | 2021-09-10 | Basf Se | Composite foils biodisintegratable at home compost conditions |
WO2022179912A1 (en) | 2021-02-24 | 2022-09-01 | Basf Se | Adhesive labels comprising biodegradable aqueous polyurethane pressure-sensitive adhesive |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2788447B1 (de) | 2011-12-09 | 2015-09-16 | Basf Se | Verwendung von wässrigen polyurethandispersionen zur verbundfolienkaschierung |
US9005762B2 (en) | 2011-12-09 | 2015-04-14 | Basf Se | Use of aqueous polyurethane dispersions for composite foil lamination |
JP2016224116A (ja) * | 2015-05-27 | 2016-12-28 | シャープ株式会社 | 表示パネルの製造方法 |
EP4116347A1 (de) | 2021-07-07 | 2023-01-11 | Covestro Deutschland AG | Zweikomponentige polyurethandispersionsklebstoffe |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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EP0498218A2 (de) * | 1991-02-05 | 1992-08-12 | Bayer Ag | Wässrige Polyurethan-Dispersionen und ihre Verwendung als Kaschierklebstoffe |
DE4308079A1 (de) * | 1993-03-13 | 1994-09-15 | Basf Ag | Verwendung von wäßrigen Polyurethandispersionen als Verbundfolienklebstoff |
DE4343895A1 (de) * | 1993-12-22 | 1995-06-29 | Henkel Kgaa | Verfahren zur Herstellung von Polyurethandispersionen |
US6235384B1 (en) * | 1998-06-04 | 2001-05-22 | H. B. Fuller Licensing & Financing, Inc. | Aqueous laminating adhesive composition and a method of using thereof |
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US4879032A (en) * | 1984-06-04 | 1989-11-07 | Allied Resin Corporation | Fluid separatory devices having improved potting and adhesive compositions |
US5250510A (en) * | 1987-07-25 | 1993-10-05 | Sumitomo Electric Industries Ltd. | Superconducting material |
DE4003422A1 (de) * | 1990-02-06 | 1991-08-08 | Basf Ag | Waessrige polyurethanzubereitungen |
US5091239A (en) * | 1990-03-07 | 1992-02-25 | Cms Gilbreth Packaging Systems, Inc. | Methods and adhesives for bonding polyolefin film |
JP3178543B2 (ja) * | 1991-11-13 | 2001-06-18 | 大日本インキ化学工業株式会社 | ポリウレタン樹脂水性分散体の製造方法 |
JPH06136085A (ja) * | 1992-10-21 | 1994-05-17 | Mitsui Toatsu Chem Inc | 内部架橋型水性ウレタン樹脂の製造方法 |
JPH06145598A (ja) * | 1992-11-13 | 1994-05-24 | Dainippon Ink & Chem Inc | 水性コーティング剤 |
US5834554A (en) * | 1996-03-05 | 1998-11-10 | H. B. Fuller Licensing & Financing, Inc. | Laminating adhesives for flexible packaging |
JP3706198B2 (ja) * | 1996-04-19 | 2005-10-12 | 三洋化成工業株式会社 | 水性印刷インキ用バインダ− |
JP2896995B2 (ja) * | 1996-06-25 | 1999-05-31 | 三洋化成工業株式会社 | 印刷インキ用バインダ−および印刷インキ |
JP2005272775A (ja) * | 2004-03-26 | 2005-10-06 | Toyo Mooton Kk | 水性一液ウレタン樹脂接着剤の製造方法 |
-
2005
- 2005-02-19 DE DE200510006235 patent/DE102005006235A1/de not_active Withdrawn
-
2006
- 2006-02-15 MX MX2007009191A patent/MX2007009191A/es active IP Right Grant
- 2006-02-15 EP EP06708294.1A patent/EP1853640B1/de active Active
- 2006-02-15 PL PL06708294T patent/PL1853640T3/pl unknown
- 2006-02-15 CN CNA2006800051596A patent/CN101120031A/zh active Pending
- 2006-02-15 BR BRPI0607767A patent/BRPI0607767B1/pt not_active IP Right Cessation
- 2006-02-15 JP JP2007555606A patent/JP2008530329A/ja active Pending
- 2006-02-15 ES ES06708294.1T patent/ES2534997T3/es active Active
- 2006-02-15 KR KR1020077021378A patent/KR20070114169A/ko not_active Application Discontinuation
- 2006-02-15 US US11/815,901 patent/US20080145671A1/en not_active Abandoned
- 2006-02-15 WO PCT/EP2006/050968 patent/WO2006087348A1/de active Application Filing
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
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EP0498218A2 (de) * | 1991-02-05 | 1992-08-12 | Bayer Ag | Wässrige Polyurethan-Dispersionen und ihre Verwendung als Kaschierklebstoffe |
DE4308079A1 (de) * | 1993-03-13 | 1994-09-15 | Basf Ag | Verwendung von wäßrigen Polyurethandispersionen als Verbundfolienklebstoff |
DE4343895A1 (de) * | 1993-12-22 | 1995-06-29 | Henkel Kgaa | Verfahren zur Herstellung von Polyurethandispersionen |
US6235384B1 (en) * | 1998-06-04 | 2001-05-22 | H. B. Fuller Licensing & Financing, Inc. | Aqueous laminating adhesive composition and a method of using thereof |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10240071B2 (en) | 2014-12-05 | 2019-03-26 | Basf Se | Aqueous adhesive dispersion containing polyurethanes and ethoxylated fatty alcohols |
WO2021175676A1 (en) | 2020-03-02 | 2021-09-10 | Basf Se | Composite foils biodisintegratable at home compost conditions |
WO2022179912A1 (en) | 2021-02-24 | 2022-09-01 | Basf Se | Adhesive labels comprising biodegradable aqueous polyurethane pressure-sensitive adhesive |
Also Published As
Publication number | Publication date |
---|---|
BRPI0607767A2 (pt) | 2010-03-23 |
US20080145671A1 (en) | 2008-06-19 |
EP1853640A1 (de) | 2007-11-14 |
EP1853640B1 (de) | 2015-01-21 |
ES2534997T3 (es) | 2015-05-04 |
DE102005006235A1 (de) | 2006-08-31 |
PL1853640T3 (pl) | 2015-06-30 |
CN101120031A (zh) | 2008-02-06 |
MX2007009191A (es) | 2007-08-22 |
KR20070114169A (ko) | 2007-11-29 |
BRPI0607767B1 (pt) | 2016-09-13 |
JP2008530329A (ja) | 2008-08-07 |
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