WO2009115369A1 - Strahlenhärtbare formulierungen - Google Patents
Strahlenhärtbare formulierungen Download PDFInfo
- Publication number
- WO2009115369A1 WO2009115369A1 PCT/EP2009/051299 EP2009051299W WO2009115369A1 WO 2009115369 A1 WO2009115369 A1 WO 2009115369A1 EP 2009051299 W EP2009051299 W EP 2009051299W WO 2009115369 A1 WO2009115369 A1 WO 2009115369A1
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- WO
- WIPO (PCT)
- Prior art keywords
- radiation
- curable
- acrylates
- optionally
- formulations according
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 61
- 238000009472 formulation Methods 0.000 title claims abstract description 57
- 238000000576 coating method Methods 0.000 claims description 28
- 239000011248 coating agent Substances 0.000 claims description 14
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 12
- -1 hexafluoroantimonate Chemical compound 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 7
- 239000002318 adhesion promoter Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 239000000049 pigment Substances 0.000 claims description 6
- 150000004756 silanes Chemical class 0.000 claims description 5
- 238000003860 storage Methods 0.000 claims description 5
- 239000004593 Epoxy Substances 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical class OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229920000728 polyester Polymers 0.000 claims description 4
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 4
- 238000009833 condensation Methods 0.000 claims description 3
- 230000005494 condensation Effects 0.000 claims description 3
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- 230000007062 hydrolysis Effects 0.000 claims description 3
- 238000006460 hydrolysis reaction Methods 0.000 claims description 3
- 239000011229 interlayer Substances 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 229920000570 polyether Polymers 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 2
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 2
- BOXSCYUXSBYGRD-UHFFFAOYSA-N cyclopenta-1,3-diene;iron(3+) Chemical compound [Fe+3].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 BOXSCYUXSBYGRD-UHFFFAOYSA-N 0.000 claims description 2
- 239000012955 diaryliodonium Substances 0.000 claims description 2
- 125000005520 diaryliodonium group Chemical group 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- 125000003709 fluoroalkyl group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 239000003999 initiator Substances 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 125000005358 mercaptoalkyl group Chemical group 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 229920000058 polyacrylate Polymers 0.000 claims description 2
- 229910000077 silane Inorganic materials 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 230000007797 corrosion Effects 0.000 abstract description 10
- 238000005260 corrosion Methods 0.000 abstract description 10
- 239000000758 substrate Substances 0.000 abstract description 10
- 229910052751 metal Inorganic materials 0.000 abstract description 6
- 239000002184 metal Substances 0.000 abstract description 6
- 230000005855 radiation Effects 0.000 description 13
- 238000001723 curing Methods 0.000 description 11
- 238000005516 engineering process Methods 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 9
- 238000003847 radiation curing Methods 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- 239000003085 diluting agent Substances 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 5
- 238000004132 cross linking Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 150000003254 radicals Chemical class 0.000 description 5
- 238000010894 electron beam technology Methods 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 239000003973 paint Substances 0.000 description 4
- 239000000976 ink Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 2
- VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- CWAFVXWRGIEBPL-UHFFFAOYSA-N ethoxysilane Chemical class CCO[SiH3] CWAFVXWRGIEBPL-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- MYWOJODOMFBVCB-UHFFFAOYSA-N 1,2,6-trimethylphenanthrene Chemical compound CC1=CC=C2C3=CC(C)=CC=C3C=CC2=C1C MYWOJODOMFBVCB-UHFFFAOYSA-N 0.000 description 1
- ZDQNWDNMNKSMHI-UHFFFAOYSA-N 1-[2-(2-prop-2-enoyloxypropoxy)propoxy]propan-2-yl prop-2-enoate Chemical compound C=CC(=O)OC(C)COC(C)COCC(C)OC(=O)C=C ZDQNWDNMNKSMHI-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- RZVINYQDSSQUKO-UHFFFAOYSA-N 2-phenoxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC1=CC=CC=C1 RZVINYQDSSQUKO-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- URDOJQUSEUXVRP-UHFFFAOYSA-N 3-triethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CCO[Si](OCC)(OCC)CCCOC(=O)C(C)=C URDOJQUSEUXVRP-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- XDLMVUHYZWKMMD-UHFFFAOYSA-N 3-trimethoxysilylpropyl 2-methylprop-2-enoate Chemical compound CO[Si](OC)(OC)CCCOC(=O)C(C)=C XDLMVUHYZWKMMD-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- BOTDANWDWHJENH-UHFFFAOYSA-N Tetraethyl orthosilicate Chemical compound CCO[Si](OCC)(OCC)OCC BOTDANWDWHJENH-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 238000003848 UV Light-Curing Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 235000019820 disodium diphosphate Nutrition 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- RSKGMYDENCAJEN-UHFFFAOYSA-N hexadecyl(trimethoxy)silane Chemical compound CCCCCCCCCCCCCCCC[Si](OC)(OC)OC RSKGMYDENCAJEN-UHFFFAOYSA-N 0.000 description 1
- 230000008595 infiltration Effects 0.000 description 1
- 238000001764 infiltration Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- FSDNTQSJGHSJBG-UHFFFAOYSA-N piperidine-4-carbonitrile Chemical compound N#CC1CCNCC1 FSDNTQSJGHSJBG-UHFFFAOYSA-N 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- QCTJRYGLPAFRMS-UHFFFAOYSA-N prop-2-enoic acid;1,3,5-triazine-2,4,6-triamine Chemical class OC(=O)C=C.NC1=NC(N)=NC(N)=N1 QCTJRYGLPAFRMS-UHFFFAOYSA-N 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Chemical class 0.000 description 1
- MUTNCGKQJGXKEM-UHFFFAOYSA-N tamibarotene Chemical compound C=1C=C2C(C)(C)CCC(C)(C)C2=CC=1NC(=O)C1=CC=C(C(O)=O)C=C1 MUTNCGKQJGXKEM-UHFFFAOYSA-N 0.000 description 1
- LFQCEHFDDXELDD-UHFFFAOYSA-N tetramethyl orthosilicate Chemical compound CO[Si](OC)(OC)OC LFQCEHFDDXELDD-UHFFFAOYSA-N 0.000 description 1
- CPUDPFPXCZDNGI-UHFFFAOYSA-N triethoxy(methyl)silane Chemical compound CCO[Si](C)(OCC)OCC CPUDPFPXCZDNGI-UHFFFAOYSA-N 0.000 description 1
- HQYALQRYBUJWDH-UHFFFAOYSA-N trimethoxy(propyl)silane Chemical compound CCC[Si](OC)(OC)OC HQYALQRYBUJWDH-UHFFFAOYSA-N 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
Definitions
- the present invention relates to the use of alkoxysilane components in free-radically radiation-curable formulations which, when cured, offer, in particular, corrosion protection for metallic substrates.
- Coating of metallic substrates presents a particular problem for radiation curable formulations, as loss of adhesion may occur due to shrinkage processes. Therefore, phosphoric acid-containing adhesion promoters are often used for such substrates. Examples are US 5,128,387 (coating of beer cans) and JP 2001172554 (coating of various doses).
- epoxy acrylates have excellent adhesion and good corrosion protection on metal substrates. Disadvantage of such coatings but is the low deformability after curing.
- coating technologies e.g. As coil coating, the deformability of the coated workpieces without formation of cracks in the coating is crucial. In addition, such coatings tend to yellow due to their aromatic components.
- WO 03/022945 describes low-viscosity radiation-curable formulations for metal substrates based on radiation-curable resins, monofunctional reactive diluents and acidic coupling agents.
- the resins used are customary, available from various suppliers sales products.
- EP 902 040 also relates to radiation-curable formulations. It describes urethane (meth) acrylates with monofunctional esters of an unsaturated carboxylic acid esterified with alcohols containing a carbocycle or a heterocycle.
- the object of the present invention is to find radiation-curable, free-radically crosslinking formulations which, on the one hand, are readily deformable after the coating, that is to say flexible, but on the other hand also ensure excellent corrosion protection for metal substrates.
- Radiation-curable free-radically crosslinking formulations in the sense of the present invention means formulations which can be cured by means of UV radiation, electron beams, microwave radiation, laser radiation or by means of plasma.
- the present invention provides the use of at least one alkoxysilane component and at least one acid-generating photon initiator in radiation-curable, radically crosslinkable formulations, in particular in paints.
- radiation-curable, radically crosslinkable formulations are likewise provided by the present invention.
- a preferred radiation-curable formulation according to the present invention is in particular those consisting of A) at least one radiation-curable radically crosslinkable component, B) at least 2% by weight of at least one alkoxysilane component, based on the overall formulation, C) at least one acid-generating photoinitiator, D) optionally one or more adhesion promoters, E) optionally one or more photoinitiators for radical curing, and F) optionally one or more pigments and other additives.
- the radiation-curable formulations according to the invention have the advantage that, when used, improved corrosion protection is achieved with constant good flexibility.
- An essential component of the formulations according to the invention is the radiation-curable free-radically crosslinkable component A).
- component A are monomeric, oligomeric or polymeric compounds in question. Suitable oligomeric and polymeric compounds are often referred to as resins.
- the resins A) may be, for example, epoxy acrylates, polyester acrylates, polyether acrylates, polyacrylate acrylates, and urethane acrylates, alone or in the form of mixtures. In the case of Urethanacrylate these z. B. on polyesters or else based on polyethers. The corresponding methacrylates are also known.
- Other polymerizable groups are epoxides and vinyl ethers. These can also be attached to different base resins.
- a radiation-curable, radically crosslinkable component A it is also possible to use monomers, so-called reactive diluents. These are usually acrylate or methacrylate-containing substances which are liquid at room temperature and thus able to lower the overall viscosity of the formulation.
- Examples of such products are in particular isobornyl acrylate, hydroxypropyl methacrylate, trimethylolpropane formal monoacrylate, tetrahydrofurfuryl acrylate, phenoxyethyl acrylate trimethylenepropane triacrylate, dipropylene glycol diacrylate, tripropylene glycol diacrylate, hexanediol diacrylate, pentaerythritol tetraacrylate, lauryl acrylate and also propoxylated or ethoxylated variants of these reactive diluents and / or urethanized reactive diluents such as EBECRYL 1039 (Cytec) and others.
- other liquid components which are capable of reacting under free radical polymerization conditions, e.g. As vinyl ethers or allyl ethers.
- the amount A) in the formulation varies from 5 to 95% by weight, preferably from 10 to 85% by weight.
- Polyester urethane acrylates are particularly preferred in the resins. Examples are Dynapol R 110 IBOA 75 (commercial product of Evonik Degussa GmbH, Germany, Coatings & Additives) and EBECRYL 1256 (commercial product of Cytec).
- EBECRYL 1256 commercial product of Cytec.
- the reactive diluents particular preference is given to isobornyl acrylate and hexanediol diacrylate.
- alkoxysilane component (B) Another essential component of the formulations according to the invention is the alkoxysilane component (B).
- the proportion of alkoxysilane components B) in the overall formulation is in particular 2-25% by weight, preferably 4-15% by weight.
- Suitable alkoxysilane components B) are, for example, compounds selected from the group comprising organofunctional silanes of the general formula I.
- R 1 is a linear, branched or cyclic, optionally substituted Alkyl group having 1 to 20 carbon atoms, for example substituted with N-, O-, S-, halogen-bearing groups such as fluoroalkyl, aminoalkyl, mercaptoalkyl, methacryloxyalkyl or OR, ie OH or alkoxy, in particular methoxy or ethoxy, wherein R is 'Methyl is, groups R are independently a hydrogen or a linear, branched or cyclic alkyl group having 1 to 6 carbon atoms and n is 0 or 1.
- methoxy- or ethoxysilanes which are in particular a functional group R 1 from the series methoxy, ethoxy, methyl, ethyl, n-propyl, i-propyl, n-butyl, n-octyl, i-octyl, Thdecafluoro-1,1,2,2-tetrahydroctyl - to name but a few examples - carry, for example but not limited to, methylthmethoxysilane, methyltriethoxysilane, vinylthmethoxysilane, vinyltriethoxysilane, n-propyltrimethoxysilane, n-propylthethoxysilane, n-octylthmethoxysilane, n-octylthethoxysilane , Hexadecyltrimethoxysilane, hexadecyltrimethoxysilane, hex
- the alkoxysilane component B) may be selected from compounds of the group comprising epoxy-functional silanes of the general formula II
- R, R 'and R are each a hydrogen (H) or a linear, branched or cyclic, optionally substituted alkyl group having 1 to 6 C atoms, preferably H, methyl, ethyl, n-propyl, n-butyl, groups A and A 'are the same or and each represents a bivalent alkyl group having 1 to 10 carbon atoms, preferably - (CH 2 ) -, - (CH 2 ) 2 -, - (CH 2 ) 3 -, - (CH 2 ) (CH) ( CH 3 ) (CH 2 ) - for A 'and - (CH 2 ) - for A, and m is 0 or 1.
- the glycidylpropylalkoxysilane of the general formula II is glycidyloxypropylthmethoxy- or ethoxysilane.
- alkoxysilane components are mixtures of compounds of the general formula I and / or II and in particular also oligomeric siloxane components, in particular obtainable by controlled hydrolysis and condensation of at least one epoxy-functional silane of the general formula II, if appropriate in the presence of compounds of the formula I.
- the said oligomeric siloxane components are obtained in particular by hydrolysis and condensation of corresponding silanes in the presence of boric acid.
- Such alkoxysilane components which are particularly suitable in the present invention are described, for example, in DE 102007038314.4, the disclosure of which is incorporated by reference in the present invention.
- Acid generating photoinitiators C are z.
- Acid generating photoinitiators C are z.
- Such photoinitiators are disclosed for example, in the patent documents WO 98/18868, WO 95/17476, US 5,721,020, EP 0721477, EP 0825218, EP 0764691, EP 0764690, EP 0736555, EP 0688804 and EP 0667381, the disclosure of which in the present invention by reference is included.
- These are usually compounds from the group comprising diaryliodonium, ferrocenium or triarylsulphonium salts with hexafluoroantimonate, hexafluorophosphate or tetrafluoroborate anions.
- photoinitiators which generate radiation under UV radiation or electron radiation are Deuteron UV 1240, UV 1242 and UV 2257, all from Deuteron, and Irgacure 250, CIBA.
- the amount of C) is generally 0.5 to 5 wt .-%, preferably 1 -3 wt .-%, based on the total formulation.
- the radiation generated by radiation accelerates the curing of alkoxysilanes, thus increasing the crosslinking density and also improves the adhesion-promoting action of the alkoxysilanes.
- the formulations according to the invention may contain adhesion promoter D).
- adhesion promoters for radiation-curable formulations for metallic substrates consist of phosphoric acid and / or phosphonic acid and / or their reaction products (eg esters) with functionalized acrylates. While the free phosphoric acid groups are responsible for direct adhesion to the metal, the acrylate groups provide a bond with the coating matrix.
- reaction products eg esters
- the free phosphoric acid groups are responsible for direct adhesion to the metal
- the acrylate groups provide a bond with the coating matrix.
- Such products are described, for example, in WO 01/98413, JP 08231564, and JP 06313127, the disclosure of which is incorporated herein by reference.
- Typical commercial products are EBECRYL 169 and 170 from Cytec, ALDITOL VxI 6219 from VIANOVA, CD 9050 and CD 9052 from Sartomer, SIPOMER PAM-100, SIPOMER PAM-200 and SIPOMER PAM-300 from Rhodia and GENORAD 40 from Rahn.
- the amount of C) in the formulation is from 0.1 to 10% by weight, preferably from 1 to 5% by weight.
- photoinitiators for radical curing E can be present.
- Suitable photoinitiators and their preparation are z. In "Radiation Curing in Polymer Science & Technology, Vol II: Photoinitiating Systems" by JP Fouassier, JF Rabek, Elsevier Applied Science, London and New York, 1993, p. 1 - 374, described. These are often ⁇ -hydroxy ketones or derivatives of these.
- the photoinitiators, if present, may be present in amounts of 0.2 to 10% by weight.
- Such radical-generating photoinitiators accelerate the curing under UV radiation, but are not required when using electron beams, since the starting radicals are also formed without photoinitiators.
- Suitable pigments F) for radiation-curable formulations according to the present invention are, for. As described in "Radiation Curing in Polymer Science & Technology, Vol IV: Practical Aspects and Application” by JP Fouassier, JF Rabek, Elsevier Applied Science, London and New York, 1993, Chapter 5, pages 87 to 105, and may be used in amounts Examples of anticorrosive pigments can be found, for example, in Pigment + Filler Tables, O. Lückert, Vincentz Verlag Hannover, 6th edition, 2002.
- Examples include: SHIELDEX C 303 (Grace Davison) and HALOX Coil X 100, HALOX Coil X 200 and HALOX CW 491 (Erbslöh), HEUCOPHOS SAPP or also ZPA (Heubach), K-White TC 720 (Tayca) and HOMBICOR (Sachtleben) Naturally, simple inorganic salts such as e.g. As zinc phosphate into consideration.
- additives F) for radiation-curable formulations are available in various compositions and for various purposes, eg. B. leveling agents, matting agents, degassing agents and others.
- the formulations according to the invention are prepared by mixing the individual formulation constituents. All types known to those skilled in the art for producing such formulations are suitable for this purpose. In the simplest embodiment, those described above Formulation ingredients by means of a stirrer, z. B of a magnetic stirrer, mixed together.
- Another object of the present invention is the use of the radiation-curable formulations of the invention as a primer, interlayer, topcoat, clearcoat and / or in coatings. Particularly preferred is the use of a radiation-curable formulation consisting of
- F optionally pigments and other additives, as a primer, interlayer, topcoat and / or clearcoat.
- the application of the radiation-curable formulation can be done by application techniques known in paint technology, for. As doctoring, rolling, spraying or spraying.
- a metallic substrate is mainly steel, optionally pretreated, but also aluminum and other metals or alloys, which are provided for corrosion protection reasons with a coating.
- the curing takes place in the presence of photoinitiators under UV light or in the absence of photoinitiators by radical curing under electron beams. Curing in the plasma or under microwave irradiation is also possible. The properties of the cured coatings are largely independent of the curing method.
- UV curing and UV lamps are z.
- Electron Beam Hardening and Hardening are described, for example, in “Radiation Curing in Polymer Science & Technology, Vol I: Fundamentals and Methods” by JP Fouassier, JF Rabek, Elsevier Applied Science, London and New York, 1993, Chapter 4, pp. 193 to 225 and in US Pat Chapter 9, pages 503 to 555.
- the invention likewise relates to the use of a radiation-curable formulation according to the invention for the production of coatings by the coil coating method, wherein the previously described preferred forms can also be used for this subject of the present invention.
- Another object of the present invention are coatings containing or based on radiation-curable formulations according to the present invention.
- the hardened coatings comprising or based on radiation-curable formulations are also included.
- the coating according to the invention can either be used alone or be a layer of a multi-layer structure. It can be applied, for example, as a primer, as an intermediate layer or as a topcoat or clearcoat.
- the over or under the coating of the invention lying Layers can either be thermally cured conventionally or else by radiation.
- the ready-to-use formulation is knife-coated onto steel sheets (Bonder sheets 1303) and subsequently cured under a UV lamp (3 m / min, minicure, mercury-vapor lamp, 80 W / cm, Technigraf).
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Silicon Polymers (AREA)
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL09722353T PL2254921T3 (pl) | 2008-03-18 | 2009-02-05 | Formulacje utwardzalne promieniowaniem |
MX2010010170A MX2010010170A (es) | 2008-03-18 | 2009-02-05 | Formulaciones curables por radiacion. |
EP09722353A EP2254921B1 (de) | 2008-03-18 | 2009-02-05 | Strahlenhärtbare formulierungen |
RU2010142225/05A RU2499811C2 (ru) | 2008-03-18 | 2009-02-05 | Отверждаемые излучением составы |
AT09722353T ATE555143T1 (de) | 2008-03-18 | 2009-02-05 | Strahlenhärtbare formulierungen |
JP2011500135A JP2011517465A (ja) | 2008-03-18 | 2009-02-05 | 放射線硬化性配合物 |
US12/933,028 US8642673B2 (en) | 2008-03-18 | 2009-02-05 | Radiation-curable formulations |
AU2009226810A AU2009226810A1 (en) | 2008-03-18 | 2009-02-05 | Radiation-curable formulations |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102008000721A DE102008000721A1 (de) | 2008-03-18 | 2008-03-18 | Strahlenhärtbare Formulierungen |
DE102008000721.8 | 2008-03-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2009115369A1 true WO2009115369A1 (de) | 2009-09-24 |
Family
ID=40497598
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2009/051299 WO2009115369A1 (de) | 2008-03-18 | 2009-02-05 | Strahlenhärtbare formulierungen |
Country Status (13)
Country | Link |
---|---|
US (1) | US8642673B2 (de) |
EP (1) | EP2254921B1 (de) |
JP (1) | JP2011517465A (de) |
KR (1) | KR20100137469A (de) |
CN (1) | CN101538425B (de) |
AT (1) | ATE555143T1 (de) |
AU (1) | AU2009226810A1 (de) |
DE (1) | DE102008000721A1 (de) |
MX (1) | MX2010010170A (de) |
PL (1) | PL2254921T3 (de) |
RU (1) | RU2499811C2 (de) |
TW (1) | TW201002770A (de) |
WO (1) | WO2009115369A1 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013049744A (ja) * | 2011-08-30 | 2013-03-14 | Jsr Corp | 放射線硬化性樹脂組成物 |
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ES2740954T3 (es) | 2012-05-16 | 2020-02-07 | Univ Haute Alsace | Composición curable radical y catiónicamente por radiación y método para preparar una capa híbrida sol-gel en una superficie de un sustrato usando dicha composición |
WO2013171582A1 (en) | 2012-05-16 | 2013-11-21 | Université De Haute-Alsace | Radiation curable composition, and method for preparing a hybrid sol-gel layer on a surface of a substrate using said composition |
MX2016013185A (es) | 2014-04-10 | 2017-01-16 | 3M Innovative Properties Co | Revestimiento promotor de adhesion y/o de supresion de polvo. |
JP6517077B2 (ja) * | 2015-04-28 | 2019-05-22 | 富士フイルム株式会社 | 硬化性組成物、硬化膜、有機el表示装置、液晶表示装置、タッチパネル及びタッチパネル表示装置 |
KR101731703B1 (ko) * | 2015-04-30 | 2017-05-02 | 삼성에스디아이 주식회사 | 윈도우 필름용 조성물, 이로부터 형성된 플렉시블 윈도우 필름 및 이를 포함하는 플렉시블 디스플레이 장치 |
WO2018160203A1 (en) * | 2017-03-01 | 2018-09-07 | Ppg Industries Ohio, Inc. | Corrosion inhibitors and coating compositions containing the same |
EP3375827A1 (de) * | 2017-03-17 | 2018-09-19 | TIGER Coatings GmbH & Co. KG | Laminat-tinte |
JP7370816B2 (ja) * | 2019-11-01 | 2023-10-30 | 古河電気工業株式会社 | 被膜材、これを用いた樹脂被膜構造及び端子付き電線 |
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-
2009
- 2009-02-05 EP EP09722353A patent/EP2254921B1/de not_active Not-in-force
- 2009-02-05 AT AT09722353T patent/ATE555143T1/de active
- 2009-02-05 JP JP2011500135A patent/JP2011517465A/ja active Pending
- 2009-02-05 AU AU2009226810A patent/AU2009226810A1/en not_active Abandoned
- 2009-02-05 RU RU2010142225/05A patent/RU2499811C2/ru not_active IP Right Cessation
- 2009-02-05 KR KR1020107020840A patent/KR20100137469A/ko not_active Application Discontinuation
- 2009-02-05 MX MX2010010170A patent/MX2010010170A/es active IP Right Grant
- 2009-02-05 WO PCT/EP2009/051299 patent/WO2009115369A1/de active Application Filing
- 2009-02-05 US US12/933,028 patent/US8642673B2/en not_active Expired - Fee Related
- 2009-02-05 PL PL09722353T patent/PL2254921T3/pl unknown
- 2009-03-12 TW TW098108062A patent/TW201002770A/zh unknown
- 2009-03-17 CN CN200910128952.0A patent/CN101538425B/zh not_active Expired - Fee Related
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013049744A (ja) * | 2011-08-30 | 2013-03-14 | Jsr Corp | 放射線硬化性樹脂組成物 |
Also Published As
Publication number | Publication date |
---|---|
DE102008000721A1 (de) | 2009-09-24 |
KR20100137469A (ko) | 2010-12-30 |
RU2499811C2 (ru) | 2013-11-27 |
EP2254921A1 (de) | 2010-12-01 |
US20110060068A1 (en) | 2011-03-10 |
CN101538425B (zh) | 2014-10-29 |
US8642673B2 (en) | 2014-02-04 |
CN101538425A (zh) | 2009-09-23 |
PL2254921T3 (pl) | 2012-09-28 |
EP2254921B1 (de) | 2012-04-25 |
JP2011517465A (ja) | 2011-06-09 |
MX2010010170A (es) | 2010-10-04 |
RU2010142225A (ru) | 2012-04-27 |
AU2009226810A1 (en) | 2009-09-24 |
ATE555143T1 (de) | 2012-05-15 |
TW201002770A (en) | 2010-01-16 |
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