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EP1664226A1 - Liant a proprietes barriere - Google Patents

Liant a proprietes barriere

Info

Publication number
EP1664226A1
EP1664226A1 EP04765281A EP04765281A EP1664226A1 EP 1664226 A1 EP1664226 A1 EP 1664226A1 EP 04765281 A EP04765281 A EP 04765281A EP 04765281 A EP04765281 A EP 04765281A EP 1664226 A1 EP1664226 A1 EP 1664226A1
Authority
EP
European Patent Office
Prior art keywords
group
radical
weight
component
nco
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP04765281A
Other languages
German (de)
English (en)
Inventor
Günter Henke
Kamil Kalus
Annabelle Guilleux
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Henkel AG and Co KGaA
Original Assignee
Henkel AG and Co KGaA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Henkel AG and Co KGaA filed Critical Henkel AG and Co KGaA
Publication of EP1664226A1 publication Critical patent/EP1664226A1/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • 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
    • C09J175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
    • C09J175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—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
    • C08G18/67—Unsaturated compounds having active hydrogen
    • C08G18/671—Unsaturated compounds having only one group containing active hydrogen
    • C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group 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
    • 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
    • C08G18/81—Unsaturated isocyanates or isothiocyanates
    • C08G18/8141—Unsaturated isocyanates or isothiocyanates masked
    • C08G18/815—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen
    • C08G18/8158—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen
    • C08G18/8175—Polyisocyanates or polyisothiocyanates masked with unsaturated compounds having active hydrogen with unsaturated compounds having only one group containing active hydrogen with esters of acrylic or alkylacrylic acid having only one group containing active hydrogen
    • 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
    • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04—Polyurethanes
    • C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
    • C09D175/16—Polyurethanes having carbon-to-carbon unsaturated bonds having terminal carbon-to-carbon unsaturated bonds

Definitions

  • the invention relates to binders with barrier properties, their use for gluing, coating and sealing, a method for producing composite materials using the binders according to the invention with barrier properties and the use of these composite materials for packaging.
  • multi-layer systems with separate barrier layers are constructed by combining polyvinylidene chloride (PVDC), ethylene vinyl alcohol (EVOH) and / or aluminum foils with polyethylene foils, polyester foils and / or polyvinyl chloride foils.
  • PVDC polyvinylidene chloride
  • EVOH ethylene vinyl alcohol
  • aluminum foils with polyethylene foils, polyester foils and / or polyvinyl chloride foils.
  • These multilayer systems can be built up either by coextrusion or by gluing separately manufactured foils.
  • packaging films e.g. based on polyethylene terephthalate or biaxially oriented polypropylene, with an aluminum and / or silicon oxide layer (in a vacuum).
  • Another known method uses the surface finishing of the flexible packaging films by coating the films with solvent- or water-based polyvinylidene chloride solutions or dispersions.
  • Coating agents and adhesives based on PVDC or EVOH often have inadequate adhesive strength on polyolefin films.
  • Composites of polyolefin films with such adhesives can already be separated by hand. If necessary, a primer must therefore be applied in an upstream process step in order to bring about a good adhesion of the surface coating or the adhesive to the substrate film.
  • Solvent-free polyurethane adhesives are known from EP 0906944 A2, which have barrier properties against oxygen and moisture. These polyurethane adhesives are obtainable by reacting a linear diol with a linear polyester to form a crystalline hydroxyl-terminated polyester which is reacted with a liquid diisocyanate at an NCO / OH ratio between approximately 1 and approximately 1.1. The polyurethane adhesives thus obtained are used as laminating adhesives. The disadvantage is that this type of coating material often does not have the desired flexibility. Another disadvantage is that long reaction times are required in order to achieve high barrier properties.
  • WO 02/26908 describes laminating adhesive compositions based on polymeric binders, in particular based on one- or two-component polyurethane adhesives, which contain fillers with a platelet-like crystallite structure with aspect ratios> 100 in the binder matrix.
  • the laminating adhesives show a considerable reduction in the oxygen transmission rate.
  • the packing is, for example, in the hydroxyl group. Dispersed component of the 2-component adhesive. It cannot be completely ruled out that the packing will sediment after a long period of storage, which can lead to a reduced or uneven barrier effect of the adhesive during subsequent application. The cure speed may also be too slow for some applications.
  • the present invention has for its object to improve the processing and use properties of binders with barrier properties.
  • a further object of the invention was to provide binders with barrier properties, in particular with respect to CO 2 , O 2 , N 2 , water vapor and flavoring agents, which, at low temperatures, that is to say at about 30 ° C. to about 160 ° C., preferably about 40 ° C to 120 ° C, can be applied and have good initial tack.
  • the binders are said to be particularly suitable as laminating adhesives for food packaging.
  • the shrinkage should be as low as possible during the hardening process.
  • the adhesion to surfaces that are difficult to wet should be improved.
  • the use of the binder according to the invention with barrier properties with respect to CO 2 , O 2 , N 2 , water vapor and aromatic substances as a sealant or adhesive reduces the number of production steps for the production of composite materials with barrier properties, since additional coatings with polyvinylidene chloride and / or ethylene vinyl alcohol -Layers or the vapor deposition with aluminum layers to achieve these barrier properties are no longer required. Due to the lack of a metal layer, the composite materials are more sorted and therefore easier to dispose of.
  • the binders according to the invention have a viscosity of 100 mPa.s to 26,000 mPa.s at 70 ° C.
  • Temperature-sensitive substrates for example polyolefin films, can thus be securely bonded without damaging the substrate.
  • the binder according to the invention is radiation-curable and is used as a dual system. Dual your systems are characterized by the fact that they are radiation-curable as well as curable by a second, independent curing mechanism.
  • binders are to be understood as meaning those substances which connect the same or different types of substrates or can themselves adhere firmly to them.
  • the "hardening" or “hardening” of a composition containing reactive functional groups is generally based on a polyreaction which is accompanied by an increase in the molecular weight of the compounds contained in the composition.
  • crosslinking reactions usually also take place at the same time.
  • the terms “hardening”, “hardening” or similar terms refer to polyreactions, such as can occur within individual components of the composition considered in each case in connection with the term.
  • the polyreaction can be a radical, anionic or cationic polymerization, polycondensation or polyaddition in which a reactive functional group can react with a suitable further functional group while increasing the molecular weight of the molecule carrying it. For example, this is the radiation-induced polymerization of a component bearing double bonds.
  • the terms also refer to polyreactions as they occur under different components of the composition under consideration can take place, for example the polyaddition of a component carrying isocyanate groups with a component carrying OH groups.
  • the terms also refer to polyreactions, such as can take place between a component of the composition under consideration and a component entering the composition due to external influence, for example the reaction between isocyanate groups and atmospheric humidity.
  • the feature “radiation-curable” is understood to mean the initiation of a polyreaction under the influence of radiation. Radiation is to be understood here to mean any type of radiation which causes irreversible crosslinking in the crosslinkable binder layer to be irradiated. UV, electron rays, visible light, but also IR radiation are particularly suitable.
  • molecular weight data relating to polymeric compounds relate to the number average molecular weight (M n ). Unless otherwise stated, all molecular weight data relate to values as can be obtained by gel permeation chromatography (GPC).
  • Component (A) can be obtained by reacting polyisocyanates with compounds which contain both at least one group reactive with NCO groups and at least one reactive functional group curable by radiation.
  • Suitable polyisocyanates are aliphatic, aromatic and / or alicyclic isocyanates with two or more, preferably two to at most about four, isocyanate groups.
  • particular preference is given to using monomeric polyisocyanates, in particular monomeric diisocyanates.
  • Suitable monomeric polyisocyanates are: 1, 5-naphthylene diisocyanate, 2,2'-, 2,4- and / or 4,4'-diphenylmethane diisocyanate (MDI), hydrogenated MDI (H ⁇ 2 MDI), allophanates ' of MDI, xylylene diisocyanate (XDI), tetramethylxylylene diisocyanate (TMXDI), 4,4'-diphenyldimethylmethane diisocyanate, di- and tetraalkylene diphenylmethane diisocyanate, 4,4'-dibenzyl diisocyanate, 1,3-phenylene diisocyanate, 1,4-phenylene diisocyanate, the isomers of tolylene diisocyanate (1-) Methyl-2,4-diisocyanato-cyclohexane, 1,6-diisocyanato- 2,2,4-trimethylhex
  • HDI dicyclohexylmethane diisocyanate
  • cyclohexane-1 4-diisocyanate
  • ethylene diisocyanate phthalic acid bis-isocyanato-ethyl ester
  • diisocyanates with reactive halogen atoms such as 1-chloromethylphenyl-2,4-diisocyanate
  • Sulfur-containing polyisocyanates are obtained, for example, by reacting 2 mol of hexamethylene diisocyanate with 1 mol of thiodiglycol or dihydroxydihexyl sulfide.
  • diisocyanates that can be used are, for example
  • Diisocyanatododecane and dimer fatty acid diisocyanate are particularly suitable:
  • Tetramethylene hexamethylene, undecane, dodecamethylene, 2,2,4-trimethylhexane
  • Polyisocyanate is 1-isocyanatomethyl-3-isocyanato-1, 5,5-trimethylcyclohexane
  • IPDI tetramethylxylylene diisocyanate
  • TXDI tetramethylxylylene diisocyanate
  • Diphenylmethane diisocyanate or mixtures thereof.
  • mixtures of polyisocyanates are used, at least one polyisocyanate with uretdione,
  • Oxadiazinetrione structure is included.
  • Polyisocyanates or polyisocyanate mixtures with are particularly preferred.
  • Allophanate structure based on HDI, IPDI and / or 2,4 ' - or 4,4'-diisocyanatodicyclohexylmethane can be prepared from diisocyanate and carbon dioxide.
  • Suitable as at least trifunctional isocyanates are polyisocyanates obtained by trimerization or oligomerization of diisocyanates or by reaction of Diisocyanates with polyfunctional compounds containing hydroxyl or amino groups are formed.
  • Isocyanates suitable for the production of trimers are the diisocyanates already mentioned, the trimerization products of the isocyanates HDI, MDI, TDI or IPDI being particularly preferred.
  • Adducts of diisocyanates and low molecular weight triols are also suitable as triisocyanates, in particular the adducts of aromatic diisocyanates and triols such as trimethylolpropane or glycerol.
  • the polymeric isocyanates such as those obtained as a residue in the distillation bottoms from the distillation of diisocyanates.
  • the polymeric MDI as is available in the distillation of MDI from the distillation residue, is particularly suitable.
  • polyurethane prepolymers with free NCO groups in particular so-called “NCO-terminated polyurethane prepolymers” as polyisocyanates.
  • Polyurethane prepolymers with free NCO groups can be obtained by reacting polyols with monomeric polyisocyanates, the monomeric polyisocyanate being used in excess.
  • a polyol is understood to be a polyfunctional alcohol, ie a compound with more than one OH group in the molecule.
  • the polyol can contain further functional groups, for example sulfo groups.
  • a variety of polyols can be used. For example, these are aliphatic polyols' with 2 to 4 OH groups per molecule.
  • the OH groups can be bound either primary or secondary.
  • Suitable aliphatic polyols include, for example, ethylene glycol, 1,2-propanediol, 1,3-propanediol, 1,4-butanediol, 1,4-butanediol, 1,3, 2,3-butanediol, 1,4-butenediol, 1,4-butynediol , Pentanediol-1, 5, and the isomeric pentanediols, pentenediols or pentindiols or mixtures of two or more thereof, hexanediol-1, 6, and the isomeric hexanediols, hexenediols or hexindiols or mixtures of two or more thereof, heptanediol-1, 7 and the isomeric heptane, heptene or heptinediols, octanediol-1, 8 and the
  • Highly functional alcohols such as glycerol, trimethylolpropane, pentaerythritol or sugar alcohols such as sorbitol or glucose, as well as oligomeric ethers of the substances mentioned with themselves or in a mixture of two or more of the compounds mentioned, for example polyglycerol with a degree of polymerization of about 2 to about, are also suitable 4.
  • polyols polyester polyols, polyether polyols, polyether polyols which have been modified by vinyl polymers, polyester polyether polyols, polcaprolactone polyols or polytetramethylene polyols are of particular importance.
  • polyester polyols are generally obtained by reacting polyfunctional alcohols with polyfunctional carboxylic acids.
  • Polyether polyols can also be used as the polyol.
  • Polyether polyols are preferably obtained by reacting low molecular weight polyols with alkylene oxides.
  • the alkylene oxides preferably have two to about four carbon atoms.
  • the reaction products of ethylene glycol, propylene glycol, the isomeric butanediols or hexanediols, as mentioned above, or mixtures of two or more thereof, with ethylene oxide, propylene oxide or butylene oxide or mixtures of two or more thereof are suitable.
  • reaction products of polyfunctional alcohols such as glycerol, trimethylolethane or trimethylolpropane, pentaerythritol or sugar alcohols or mixtures of two or more thereof, with the alkylene oxides mentioned to form polyether polyols are also suitable.
  • polyurethane prepolymers with free NCO groups based on polyester polyols or polyether polyols are preferred.
  • a polyether polyol and / or polyester polyol with a molar mass of 200 to 10,000, preferably from 200 to 6000 g / mol, particularly preferably 200 to 4000 g / mol, or a mixture of polyether polyols is particularly suitable for use as a polyol and / or polyester polyols that meet the restrictive criterion of molar mass.
  • a low-monomer polyurethane prepolymer is preferably used to prepare the organic compound (A), in the context of the present invention
  • “low-monomer” means a low concentration of the monomeric diisocyanates in the PU prepolymer with free NCO groups.
  • concentration of these so-called “residual monomers” is below one, preferably between 0 and 0.5% by weight, particularly preferably between 0 and 0.2% by weight, based on the composition of the PU prepolymer with free NCO groups.
  • Low-monomer PU prepolymers with free NCO groups are known for example from DE 4136490, WO 01/40342 and WO-97/46603 and are expressly the subject of this invention.
  • the polyisocyanates used are monomeric polyisocyanates from Group 1, 5-naphthylene diisocyanate, 2,2 ' -, 2,4- and / or 4,4'-diphenylmethane diisocyanate (MDI), the isomers of tolylene diisocyanate (TDI) , 1-isocyanatomethyl-3-isocyanato-1, 5,5-trimethylcyclohexane (IPDI), hexane-1, 6-diisocyanate (HDI)
  • TXDI Tetramethylxylylene diisocyanate
  • trimerization products of the isocyanates HDI, MDI, TDI or IPDI trimerization products of the isocyanates HDI, MDI, TDI or IPDI
  • NCO-terminated polyurethane prepolymers based on HDI, MDI, TDI or IPDI as well as mixtures thereof.
  • the polyisocyanates are reacted with compounds which contain both at least one functional group reactive with NCO groups and at least one reactive functional group curable by radiation.
  • the functional group reactive with an NCO group is a group which has an active hydrogen atom which can be determined by the Zerewittinoff test and is bound to an N, O or S atom. These include in particular the hydrogen atoms of water, carboxy, amino, imino, hydroxyl and thiol groups.
  • a reactive functional group curable by radiation is one
  • Compounds that can be used are, for example, polyacrylates, polyesters, polyethers,
  • Polycarbonates, polyacetals, polyurethanes, polyolefins, or rubber polymers such as
  • Nitrile or styrene / butadiene rubber provided that they have at least one functional group which is reactive by irradiation, preferably with UV light or with electron beams, and at least one acidic hydrogen atom.
  • the one used as component (A) contains
  • component (A) preference is given to derivatives of acrylic acid, for example the acrylates and the methacrylates, for reaction with the
  • Epoxy (meth) acrylates or polyurethane (meth) acrylates are examples of Epoxy (meth) acrylates or polyurethane (meth) acrylates.
  • (Meth) acrylaf is intended to mean an abbreviated notation for" acrylate and / or methacrylate "in the following text.
  • Y a group reactive towards NCO groups, preferably OH, COOH, SH, NH 2 , NHR 3 ;
  • R H, CH 3 ; 2
  • R saturated or unsaturated linear or branched alkylene group with 2 to 21 carbon atoms, optionally substituted with functional groups, for example with a phenoxy or acetoxy group; preferably 2 to 6 carbon atoms, in particular an ethylene, propylene, isopropylene, n-butylene, isobutylene group, or a C2-C4-alkylene oxide group, preferably an ethylene oxide and / or propylene oxide group, in particular preferably an ethylene oxide group with 2 to 10 ethylene oxide units and / or a propylene oxide group with 1 to 7 propylene oxide units.
  • R 3 linear or branched, saturated or unsaturated CrCis alkyl radical; C 5 -C 8 cycloalkyl, C 6 -C ⁇ o aryl, C 7 -C ⁇ 2 aralkyl;
  • hydroxy acrylates or methacrylates are used individually or in a mixture.
  • the amounts of polyisocyanate and (meth) acrylate of the general formula (II) can be selected in a wide range.
  • the ratio of the NCO group of the polyisocyanate to the group Y of the (meth) acrylate of the general formula (II) which is reactive toward NCO groups can be between 0.6: 1 and 20: 1.
  • the ratio NCO: Y is preferably 1.2: 1 to 10: 1
  • the molar mass of component (A) is between 100 g / mol and 10000 g / mol, preferably between 110 g / mol and 6000 g / mol and particularly preferably between 120 g / mol and 4000 g / mol.
  • the NCO value of component (A) is between 2% by weight and 30% by weight, preferably between 5% by weight and 25% by weight (determined according to Spiegelberger).
  • the silicon-organic compound which can be used as component (B) and has at least one NCO group and at least one functional group of Formula - Si (X) 3-n (I) can be obtained by reacting at least one polyisocyanate with at least one silicon-organic compound of the formula (III):
  • Y a group reactive towards NCO groups, preferably a -OH, - COOH, -SH, -NH 2 , NHR "group;
  • R " linear or branched, saturated or unsaturated C 1 -C 8 -alkyl-; C 5 - Cs-cycloalkyl, C 6 -C ⁇ o-aryl, C -C ⁇ 2 aralkyl;
  • A a linear or branched, saturated or unsaturated alkylene group with 1 to 12 C atoms, preferably a linear or
  • Examples of compounds of the formula (III) are H 2 N-CH 2 -Si (O-CH 2 -CH 3 ) 3 , HO-CH 2 -Si (OCH 3 ) 3 , HO- (CH 2 ) 3-O- CH 2 -Si (O-CH 3 ) 3, HO-CH 2 -CH 2 -O- CH 2 -Si (OCH 3 ) 3, (HO-C 2 H4) 2N-CH 2 -Si (O-CH 3 ) 3, HO- (C 2 H 4 -O) 3-C 2 H 4 -N (CH3) -CH 2 -Si (O-CH 3 ) 3l H 2 N- CH2-C 6 H4-CH2-NH- CH2-Si (O-CH 3 ) 3, HS-CH 2 -Si (O-CH 3 ) 3, H 2 N- (CH 2 ) 3-NH-CH 2 - Si (OCH 3 ) 3 , H 2 N -CH2-CH2-NH-CH2-Si (O
  • 3-aminopropyltrimethoxysilane, 3-aminopropyldimethoxymethylsilane, 3-aminopropyltriethoxysilane, 3-aminopropyldimethoxyphenylsilane and 3-aminopropyldiethoxyethylsilane, in particular 3-aminopropyltrimethoxysilane are used as the organosilicon compound of formula (III) Aminopropyltrimethoxysilane or bis (3-triethoxysilylpropyl) amine, or mixtures thereof.
  • Commercially available silanes are offered by Dynamit Nobel under the name DYNASYLAN®.
  • alkoxysilane derivatives with two or three alkoxy radicals and one or two alkyl radicals, to which functional groups can also be attached, for example amino, mercapto, methacryloxy or a nitrile group or a halogen radical such as chlorine.
  • polyisocyanates are used as polyisocyanates for the production of component (B), which were already described in the production of component (A).
  • Polyisocyanates from the group of the monomeric diisocyanates are preferably used, in particular the polyisocyanate is selected from the group: 2,4 ' and / or 4,4 ' diphenylmethane diisocyanate (MDI), isophorone diisocyanate (IPDI), hexamethylene diisocyanate (HDI),
  • TXDI Tetramethylxylylene diisocyanate
  • TDI tolylene diisocyanate
  • Mixtures of polyisocyanates and / or mixtures of the silicon-organic compound (III) can be used to produce component (B).
  • the reaction of the polyisocyanate component with the silicon-organic compound (III) takes place in a molar NCO / Y ratio of 1: 0.01 to 1, preferably 1: 0.05 to 0.7 and particularly preferably 1: 0, 1 to 0.4.
  • Component (B) contained in the binder according to the invention has an NCO value of 1-30%, preferably 10-28%, particularly preferably 15-25%, determined according to Spiegelberger, and has a molar mass of 100 g / mol to 1000 g / mol.
  • the free NCO groups contained in components (A) and (B) can react with moisture (water) or other compounds which are reactive towards NCO groups and have an acidic hydrogen atom and thus cause the formation of an organic network.
  • binders according to the invention with barrier properties to be processed in the processable state (generally liquid to highly viscous) in the desired manner and by adding water or other compounds which have an acidic hydrogen atom have (in this case called hardener) to harden.
  • the hardener is usually added immediately before application, with the processor only having a limited processing time after adding the hardener.
  • Such 1-component systems generally have the advantage over the 2-component systems that the often tedious mixing of the often viscous components before application is eliminated for the user.
  • the invention therefore also relates to a binder with barrier properties, which in the form of a 2K system as hardener (C) 0 to 90% by weight, preferably 5 to 60% by weight, of a compound having at least two functional groups each contains at least one acidic hydrogen atom.
  • the molar mass of (C) is in a range from 50 to 10,000 g / mol, preferably 50 to 6,000 g / mol and particularly preferably in a range from 50 to 3000 g / mol.
  • a hardener (C) is preferably a compound having at least two functional groups, each having at least one acidic hydrogen atom, or a mixture of two or more such compounds which can react with the NCO groups of (A) and (B).
  • Ais with the corresponding NCO groups of (A) and (B) reactive functional groups with at least one acidic hydrogen atom are particularly suitable primary or secondary amino groups, mercapto groups or OH groups.
  • the compounds which can be used as hardener (C) can each contain amino groups, mercapto groups or OH groups exclusively or in a mixture.
  • the functionality of the compounds that can be used in the hardener (C) is generally at least about two.
  • the hardener (C) preferably has a proportion of more highly functional compounds, for example with a functionality of three, four or more.
  • the total (average) functionality of the hardener (C) is, for example, about two (e.g. if only difunctional compounds are used as the hardener (C)) or more, for example about 2.1, 2.2, 2.5, 2,7, or 3. If necessary, the hardener (C) can have an even higher functionality, for example about four or more.
  • the hardener (C) preferably contains a polyol carrying at least two OH groups. Corresponding polyols already described in the present text are suitable for use as hardener (C).
  • the hardener (C) is generally used in an amount such that the ratio of functional groups of the compounds (A) and (B) reactive with the hardener (C) to with corresponding functional groups of the compounds (A) and (B) reactive groups of the hardener (C) is about 5: 1 to about 1: 1, in particular about 2: 1 to about 1: 1.
  • the functional group - Si (X) 3-n according to formula (I) of the organosilicon compound used as component (B) with at least one NCO group serves to build up an inorganic network of Si-O-Si units.
  • component (B) is preferably sensitive to hydrolysis, that is to say that in the presence of water or atmospheric moisture, the Si-X bond is decomposed with the release of appropriate cleavage products and with simultaneous crosslinking.
  • group X in formula (I) for example, amines, acid amides, oximes or alcohols are formed as cleavage products in the crosslinking taking place as a polycondensation reaction.
  • the course of the Si-O-Si network formation can z. B. by Karl Fischer titration (determination of water consumption during hydrolysis).
  • the Si-X bond is cleaved by adding the hardener.
  • Polyols in particular OH-terminated polyesters, are preferably used as hardeners. If the group X in formula (I) is, for example, an alkoxy group, preferably -OCH 3 or -OC 2 Hs, the network is formed by alcoholysis or transetherification.
  • the polycondensation or crosslinking reaction of component (B) takes place in the presence of a metal compound of the formula (IV): MR 4 X (IV) as component (D).
  • the radical R 4 which may be the same or different, is selected from halogen, alkoxy, alkoxycarbonyl and hydroxyl.
  • the binder can be used instead or in addition however, also contain compounds in which some or all of the groups R 4 of the formula (IV) have been replaced by one or more ligands L which are bonded more strongly to the metal M than the group R 4 .
  • Compounds of this type are described, for example, in DE 10044216 A1 (p. 4, lines 1 to 31). Suitable metal compounds are also known under the name "adhesion promoter" and represent one or more metal centers such as Si, Ti, Zr or Al, which are bonded to functional organic groups.
  • Titanates are commercially available from Kenrich Petrochemicals, Inc. and are available under the name “KR” or “LICA” substances. Similar to the silanes mentioned above, these reagents are compounds with alkoxy radicals and optionally additionally radicals which are substituted by functional groups and are bonded to the metal center via oxygen. The functional groups are, for example, amino, mercapto or hydroxyl groups. Suitable zirconate compounds are, for example, the compounds available as "KZ” or "LZ” reagents from Kenrich Petrochemicals, Inc., optionally with amino or mercapto groups.
  • Component (D) is used in the binder according to the invention in an amount of 0 to 12% by weight, preferably 0.5% to 10% by weight and particularly preferably 1% to 5% by weight, based on the total amount of (A) and (B) used.
  • the binders according to the invention with barrier properties are highly reactive, multistage curing binders.
  • a multistage curing binder is understood to mean a binder which is subjected to a rapid, first curing reaction in a first stage by irradiation, so that problem-free handling of the bonded, coated or sealed objects or materials is made possible. In a second curing stage, the binder then cures further until it has reached the desired final strength.
  • This basic methodology is described, for example, in DE 4041 753 A1.
  • the radiation in the first stage can be carried out by UV, electron beams, visible light, but also IR radiation.
  • the desired product properties are set via the radiation dose, in the case of IR radiation via the product temperature and the dwell time.
  • irradiation with UV light or with electron beams is preferred.
  • the binder composition contains at least one photoinitiator (E).
  • a photoinitiator (E) is preferably used which, when irradiated with light having a wavelength of about 215 to about 480 nm, is able to initiate a radical polymerization of olefinically unsaturated double bonds.
  • all commercially available photoinitiators which are compatible with the binder according to the invention are basically suitable for use as photoinitiator (E); H. result in at least largely homogeneous mixtures.
  • Type I substances that fragment.
  • examples include benzophenone, camphorquinone, quantacure (manufacturer: International Bio-Synthetics), Kayacure MBP (manufacturer Nippon Kayaku), Esacure BO (manufacturer: Fratelli Lamberti), Trigonal 14 (manufacturer: Akzo), photoinitiators from Irgacure ® -, Darocure ® - or Speedcure ® series (manufacturer: Ciba-Geigy), Darocure ® 1173 and / or Fi-4 (manufacturer: Eastman).
  • Irgacure ® 651, Irgacure ® 369, Irgacure ® 184, Irgacure ® 907, Irgacure ® 1850, Irgacure ® 1173 (Darocure ® 1173), Irgacure ® 1116, Speedcure ® EDB, Speedcure ® ITX, Irgacure ® 784 or Irgacure are particularly suitable ® 2959 or mixtures of two or more of them.
  • the binder according to the invention with barrier properties contains the photoinitiator (E) in an amount of 0 to 15% by weight, preferably 0.5 to 10% by weight particularly preferably 1 to 5% by weight, based on the total amount of the binder composition.
  • the radiation-curable binder according to the invention with barrier properties can furthermore contain as compound (F) a compound which has at least one and preferably two functional group (s) polymerizable by irradiation with UV light or with electron beams, but no NCO Group contains.
  • compound (F) has at least one group with an olefinically unsaturated double bond.
  • Particularly suitable compounds (F) are di- or higher-functional acrylate or methacrylate esters.
  • Such acrylate or methacrylate esters include, for example, esters of acrylic acid or methacrylic acid with aromatic, aliphatic or cycloaliphatic polyols or acrylate esters of polyether alcohols.
  • (Meth) acrylate esters of aliphatic polyols with 2 to about 40 carbon atoms include, for example, neopentyl glycol di (meth) acrylate, 1, 6-
  • These (meth) acrylate esters of aliphatic or cycloaliphatic diols can be modified with an aliphatic ester or an alkylene oxide.
  • the acrylates modified by an aliphatic ester include, for example, neopentylglycol hydroxypivalate di (meth) acrylate, caprolactone-modified
  • Neopentyl glycol hydroxypivalate di (meth) acrylates and the like.
  • the alkylene oxide-modified acrylate compounds include, for example, ethylene oxide-modified Neopentyl glycol di (meth) acrylates, modified propylene oxide
  • Neopentyl glycol di (meth) acrylates ethylene oxide modified 1, 6-
  • (Meth) acrylate monomers based on polyether polyols include, for example, neopentyl glycol-modified (meth) acrylates, trimethylolpropane di (meth) acrylates, polyethylene glycol di (meth) acrylates, polypropylene glycol di (meth) acrylates and the like.
  • Trifunctional and higher functional acrylate monomers include, for example, trimethylolpropane tri (meth) acrylate, pentaerythritol tri- and tetra (meth) acrylate, dipentaerythritol tetra (meth) acrylate, dipentaerytrhitol penta (meth) acrylate,
  • di-, tri- or higher-functional (meth) acrylate monomers mentioned which can be used according to the invention as component (F) are di-, tri- and tetrapropylene glycol diacrylate, neopentyl glycol propoxylate di (meth) acrylate,
  • Trimethylolpropane tri (meth) acrylate, trimethylolpropane monethoxytri (meth) acrylate and pentaerythritol triacrylate are preferred.
  • (Meth) acrylate esters based on polyols containing urethane groups can be prepared by reacting the polyols with polyisocyanates, so that at least partially OH-terminated polyurethane prepolymers are formed which are esterified with (meth) acrylic acid to give the corresponding mono- or diesters.
  • suitable compounds (F) are those compounds which are flowable at room temperature, in particular esters of acrylic acid or methacrylic acid.
  • Particularly suitable compounds are, for example, the acrylic or methacrylic acid esters of aromatic, cycloaliphatic, aliphatic, linear or branched C 4-20 monoalcohols or of corresponding ether alcohols, for example n-butyl acrylate, 2-ethylhexyl acrylate, octyl / decyl acrylate, isobomylacrylate, 3-methoxybutyl acrylate , 2-phenoxyethyl acrylate, benzyl acrylate or 2-methoxypropyl acrylate.
  • the molar mass of the compound (F) is in the range from 100 to 15,000 g / mol, preferably from 100 to 10,000 g / mol and particularly preferably from 100 to 8000 g / mol.
  • compound (F) makes up up to about 80% by weight, but preferably below, for example about 40% by weight, 30% by weight or about 20 in the radiation-curable binder with barrier properties wt .-%.
  • the use of smaller amounts is also possible, for example the radiation-curable binder according to the invention with barrier properties can also contain only 10% by weight or an amount of about 0.5 to about 8% by weight of compound (F).
  • the binder according to the invention may contain additives (G) which may have a proportion of up to about 50% by weight of the total binder.
  • additives (G) which can be used in the context of the present invention include, for example, plasticizers, stabilizers, antioxidants, dyes or fillers.
  • Plasticizers based on phthalic acid in particular dialkyl phthalates, are used as plasticizers (G1), phthalic esters esterified with an alkanol having from about 6 to about 14 carbon atoms being preferred. Di-isononyl or di-iso-tridecyl phthalate are particularly preferred.
  • plasticizers for example sucrose benzoate, diethylene glycol dibenzoate and / or diethylene glycol benzoate, in which about 50 to about 95% of all hydroxyl groups have been esterified, phosphate plasticizers, for example t-butylphenyldiphenylphosphate, polyethylene glycols and their derivatives, for example diphenylglycol poly (polyphenylene ether) ), liquid resin derivatives, for example the methyl ester of hydrogenated shark, vegetable and animal oils, for example glycerol esters of fatty acids and their polymerization products.
  • phosphate plasticizers for example t-butylphenyldiphenylphosphate
  • polyethylene glycols and their derivatives for example diphenylglycol poly (polyphenylene ether)
  • liquid resin derivatives for example the methyl ester of hydrogenated shark, vegetable and animal oils, for example glycerol esters of fatty acids and their polymerization products.
  • Stabilizers or antioxidants which can be used as additives (G2) in the context of the invention include phenols, sterically hindered phenols of high molecular weight (M n ), polyfunctional phenols, sulfur- and phosphorus-containing phenols or Amines.
  • Phenols which can be used as additives in the context of the invention are, for example, hydroquinone, hydroquinone monomethyl ether 2,3- (di-tert-butyl) hydroquinone, 1,3,5-trimethyl-2,4,6-tris (3,5-di -tert-butyl-4-hydroxybenzyl) benzene;
  • Butylated hydroxytoluene (BHT), pentaerythritol tetrakis 3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate; n-octadecyl-3,5-di-tert-butyl-4-hydroxyphenyl) propionate; 4,4-methylene bis (2,6-di-tert-butyl phenol); 4,4-thiobis (6-tert-butyl-o-cresol); 2,6-di-tert-butylphenol; 2,6-di-tert-butyl-n-methylphenol; 6- (4-hydroxyphenoxy) -2,4-bis (n-octylthio) -1, 3,5-triazine; Di-n-octadecyl 3,5-di-tert-butyl-4-hydroxybenzylphosphonates; 2- (n-
  • Octylthio ethyl-3,5-di-tert-butyl-4-hydroxybenzoate; and sorbitol hexa [3- (3,5-di-tert-butyl-4-hydroxyphenyl) propionate]; and p-hydroxydiphenylamine or N, N'-diphenylenediamine or phenothiazine.
  • the radiation-curable binder according to the invention with barrier properties can contain agents (G3) which improve the aging behavior of, in particular, bonds to a moist atmosphere.
  • Typical agents (G3) are, for example, ethylene / acrylamide comonomers or phosphorus derivatives.
  • Compounds containing carboxylic acid can also be used.
  • thermoplastic non-reactive polymers G5
  • barrier properties for example ethylene vinyl acetate (EVA), ethylene acrylic acid, ethylene methacrylate and ethylene-n-butyl acrylate copolymers If necessary, give the binder additional flexibility, toughness and strength.
  • EVA ethylene vinyl acetate
  • ethylene acrylic acid ethylene methacrylate
  • ethylene-n-butyl acrylate copolymers If necessary, give the binder additional flexibility, toughness and strength.
  • hydrophilic polymers for example polyvinyl alcohol, hydroxyethyl cellulose, hydroxypropyl cellulose, polyvinyl methyl ether, polyethylene oxide, polyvinyl pyrrolidone, polyethyloxazoline or starch or cellulose esters, in particular the acetates with a degree of substitution of less than 2.5, which, for example, affect the wettability of the can increase binders according to the invention.
  • component (F) Polymerizable by irradiation with UV light or with electron beams) ) as component (F), VII) 0 to 50% by weight of additives, selected from the group of plasticizers, stabilizers, antioxidants, dyes or fillers, as component (G). the sum of the constituents mentioned being 100% by weight.
  • the binder with barrier properties I) contains 15 to 95% by weight of component (A) as a reaction product from a low-monomer polyurethane prepolymer with free NCO groups and at least one hydroxyacrylate from the group 2-hydroxyethyl - (meth) acrylate, 2-hydroxypropyl (meth) acrylate, 3-hydroxypropyl (meth) acrylate, 6-hydroxyhexyl (meth) acrylate, the low-monomer polyurethane prepolymer being an addition product from a) at least one polyisocyanate from the group IPDI, MDI or TDI and b) represents at least one polyol with a molar mass of 150 g / mol to 2000 g / mol.
  • the low-monomer polyurethane prepolymer contains less than 0.5% by weight, preferably less than 0.3 and particularly preferably less than 0.1% by weight, of free polyisocyanate from the group IPDI, MDI or TDI, based on the total amount of PU prepolymer.
  • the binder contains 3 to 10% by weight of an at least trifunctional polyisocyanate.
  • the radiation-curable binder according to the invention with barrier properties can, depending on the required application, still contain up to 60% by weight of an inert solvent.
  • solvents known to the person skilled in the art can be used as solvents, in particular esters, ketones, halogenated hydrocarbons, alkanes, alkenes and aromatic hydrocarbons.
  • solvents are methylene chloride, trichlorethylene, toluene, xylene, butyl acetate, amylacetate, isobutyl acetate, methyl isobutyl ketone, methoxybutyl acetate, cyclohexane, cyclohexanone, dichlorobenzene, diethyl ketone, di-isobutyl ketone, dioxane, ethyl acetate, ethylene glycol monoethylaconyl ethylene glycol monobutyl ketone Ethyl hexyl acetate, glycol diacetate, heptane, hexane, isobutyl acetate, isooctane, isopropy
  • the radiation-curable binder according to the invention with barrier properties can be produced by customary techniques known to the person skilled in the art in the production of polymeric mixtures.
  • the hardening of the binder according to the invention includes the formation of a network which results from a combination of different network formation mechanisms: a) the construction of an inorganic network by hydrolysis / alcoholysis / transetherification and polycondensation of the organosilicon compound as component (B), b) the construction of a organic network by reaction of the free NCO groups, in particular components (A) and (B), with compounds which have an acidic hydrogen atom, c) the formation of an organic network by radiation curing.
  • the hardening of the binder leads to non-blocking, ie non-adhesive and in particular scratch-resistant coatings, fillers or sealants with flexible properties or even surface-tacky adhesives.
  • the radiation-curable binders according to the invention with barrier properties can therefore be used as coating agents, fillers, sealants or adhesives and are distinguished as adhesive seals or fillers with barrier properties with respect to CO 2 , O 2 , N 2 , gas mixtures, for example from CO 2 and N 2 , water vapor and flavors.
  • the radiation-curable binder according to the invention with barrier properties can be used for filling, sealing, coating and bonding a wide variety of materials.
  • the materials include, for example, wood, metal, glass, plant fibers, stone, paper, cellulose hydrate, plastics such as polystyrene, polyethylene, polypropylene, polyethylene terephthalate, polyvinyl chloride, copolymers of Vinyl chloride and vinylidene chloride, copolymers of vinyl acetate olefins, polyamides, or metal foils, for example made of aluminum, lead or copper.
  • the radiation-curable binder with barrier properties according to the invention can be applied to the substrate by any suitable method, for example by spraying, knife coating, 3-4-roller applicators in the case of using a solvent-free binder or 2 roller applicators in the case of using a solvent-containing binder.
  • the radiation-curable binder according to the invention with barrier properties is suitable for coating substrates made of glass, metal, plastic, paper, ceramic, etc. by dipping, pouring, brushing, spraying, electrostatic spraying, electrocoating, etc.
  • the binders are particularly suitable for coating optical, Suitable for optoelectric or electronic articles and for coating containers for fuels and heating fuels.
  • the radiation-curable binder according to the invention provides adhesives with barrier properties which are preferably suitable for the production of film composites.
  • the monomeric polyisocyanate content of less than 0.1% by weight makes the binder particularly suitable for flexible film composites which are used in the food packaging sector.
  • Another object of the present invention is therefore also a process for the production of film composites, which can be obtained by partially or fully gluing films, using the radiation-curable binder according to the invention with barrier properties.
  • the binder can be applied to the films to be bonded using machines which are usually used for such purposes, for example conventional laminating machines.
  • the application of the binder in the liquid state to a film to be bonded to a laminate, for example a film made of plastic or metal, is particularly suitable.
  • the viscosity of the binder is chosen so that it has a viscosity of approximately at typical processing temperatures 1,000 mPas to about 5,000 mPas (measured according to Brookfield, RVT DV-II digital viscometer, spindle 27).
  • Typical processing temperatures are, for example, approximately 25 to approximately 70 ° C. in the production of flexible packaging films (flexible packaging), approximately 70 to approximately 80 ° C. in the lamination of high-gloss films and approximately 80 to approximately 130 ° C. in textile applications.
  • the film coated with the solvent-containing or solvent-free radiation-curable binder with barrier properties according to the invention is first thermally crosslinked (condensed) in the drying tunnel at 40 to 120 ° C., then laminated with at least one further film, possibly under pressure, and then irradiated, or irradiated and then concealed.
  • the radiation-curable binder according to the invention with barrier properties gains in molecular weight as a result of the radiation and the crosslinking reaction associated with it, as a result of which it has more cohesion and has a tacky surface. If the irradiation is carried out by means of UV light, the binder used according to the invention contains at least one photoinitiator as component (E). The described method can be repeated several times, so that film composites can be produced which consist of more than two bonded layers.
  • the process according to the invention can be carried out under a protective gas atmosphere, that is to say in the presence of inert gases such as nitrogen.
  • a protective gas atmosphere that is to say in the presence of inert gases such as nitrogen.
  • inert gases such as nitrogen.
  • it can also advantageously be carried out without problems in a normal atmosphere, as typically prevails in the production halls.
  • Another object of the invention is a composite film, produced by the method according to the invention using the binder according to the invention.
  • the composite film is particularly suitable as a barrier film for packaging food.
  • oxygen permeability Q (O 2 ) ⁇ 100 cm 3 / (m 2 x day x bar) and the water vapor permeability Q (H 2 O) ⁇ 10 g / (m 2 x day ) at 23 ° C and 85% rel.
  • Humidity is (Delventhal, Packaging Review 3/1991, page 19-23).
  • Liotron UR 4599-22 (solvent-free) and Liotron UR 4599-21 (solvent-based): (reaction product of tripropylene glycol hexamethylene diisocyanate with hydroxy-acrylate); Henkel KGaA
  • Liotron UR 4532 polyurethane prepolymer with free isocyanate and acrylate group
  • IPDI isophorone diisocyanate
  • Dynasilan 1120 mixture of bis (3-triethoxysilylpropyl) amine and 3-aminopropyltriethoxysilane with an NCO value of 18 to 22% by weight and a viscosity of 800 to 1200 mPas (25 ° C ).
  • Liofol UR 6801 Liofol UR 6051; Liofol UR 6092, Liofol UR 6090, Liofol UR 6082, Liofol UR 6065
  • Ebecryl TPGDA tripropylene glycol diacr lat
  • the components were mixed, applied to the film material and heated to 80 ° C. in the drying tunnel.
  • the following was laminated: * film made of oriented polypropylene (OPP film), * film made of polyester (PET film), * film made of oriented polyamide (OPA film), against OPP.
  • OPP film oriented polypropylene
  • PET film polyester
  • OPA film oriented polyamide
  • the application weight of the adhesive was 2 g / m 2 in each case
  • the UV radiation was carried out by means of a UV system from Eltosch, equipped with a 120 W mercury lamp (UV dose «180 mJ / cm 2 ).
  • the laminated and irradiated material was post-cured at about 40 ° C for at least 1 day.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Sealing Material Composition (AREA)

Abstract

L'invention concerne un liant ayant des propriétés barrière, qui contient : a) un composé présentant au moins un groupe NCO et au moins un groupe fonctionnel réactif, durcissable par exposition à un rayonnement, comme constituant (A) et b) un composé organique silicium, comme constituant (B), présentant au moins un groupe NCO et au moins un groupe fonctionnel de formule (I) Si(X)3-n, dans laquelle X = -NH2 ; -NH-CO-R ; -OOC-R ; -O-N=C(R)2 ou OR' ; R = un reste alkyle C1-C18 linéaire ou ramifié, saturé ou insaturé, de préférence un reste méthyle, éthyle ou iso-propyle ; R' = R, de préférence un reste méthyle, éthyle ou iso-propyle ; ou un reste oxyalkylène ayant jusqu'à 4 atomes de C, de préférence (C2H4-O)m-H et/ou (CH2-CH(CH3)-O)m-H ; un reste cycloalkyle C5-C8 ; un reste aryle ou un reste aralkyle C7-C12 ; m = entre 1 et 40, de préférence entre 1 et 20, en particulier de préférence entre 1 et 10 ; n = 0, 1 ou 2. Ledit liant s'utilise comme liant durcissable sous l'effet de rayonnements, dans des agents de recouvrement, des charges, des matériaux d'étanchéité ou des adhésifs. L'invention concerne en outre un procédé permettant de produire des feuilles multicouche aux propriétés barrière, à l'aide du liant selon l'invention, ainsi que des feuilles multicouche obtenues d'après ledit procédé.
EP04765281A 2003-09-25 2004-09-16 Liant a proprietes barriere Withdrawn EP1664226A1 (fr)

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DE10344448A DE10344448A1 (de) 2003-09-25 2003-09-25 Bindemittel mit Barriere-Eigenschaft
PCT/EP2004/010381 WO2005033240A1 (fr) 2003-09-25 2004-09-16 Liant a proprietes barriere

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WO2005033240A1 (fr) 2005-04-14
DE10344448A1 (de) 2005-04-28
US20060162860A1 (en) 2006-07-27

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