Classifications

• • 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
• • 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
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K6/00—Preparations for dentistry
  • A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
  • A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
  • A61K6/891—Compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
  • A61K6/893—Polyurethanes
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C265/00—Derivatives of isocyanic acid
  • C07C265/14—Derivatives of isocyanic acid containing at least two isocyanate groups bound to the same carbon skeleton
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
  • C07C275/46—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylureas
  • C07C275/58—Y being a hetero atom
  • C07C275/60—Y being an oxygen atom, e.g. allophanic acids
• • 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
  • C08G18/28—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
  • C08G18/673—Esters of acrylic or alkyl acrylic acid having only one group containing active hydrogen containing two or more acrylate or alkylacrylate ester groups
• • 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
  • C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
  • C08G18/78—Nitrogen
  • C08G18/7806—Nitrogen containing -N-C=0 groups
  • C08G18/7818—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups
  • C08G18/7837—Nitrogen containing -N-C=0 groups containing ureum or ureum derivative groups containing allophanate groups
• • 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
• • 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.]

Definitions

• the invention relates to compounds with isocyanate groups or blocked isocyanate groups, allophanate groups and free-radically polymerizable CC double bonds, the CC double bonds being activated by a carbonyl group bonded directly to them or an O atom in ether function (hereinafter referred to as "activated double bonds") of polyisocyanates and alcohols A, which carry an activated double bond in addition to the alcohol group (compounds I).
• the invention relates to radiation-curable preparations and coating compositions which contain the compounds I, processes for coating with these substances and coated articles produced using these processes.
• Coating agents based on compounds containing isocyanate groups are e.g. generally known in the form of 2-component paints (cf. Kunststoff Handbuch, Volume 7, Polyurethane, 2nd edition, 1983, Carl-Hanser-Verlag Kunststoff Vienna, pages 540 - 561).
• Industrial processors of coating agent systems such as the coating industry are expected to meet a diverse range of requirements. This affects both the processing and usage properties.
• the coating agent systems In terms of processing properties, it is essential that the coating agent systems contain as little solvent as possible, but at the same time have a low viscosity.
• the low viscosity is necessary so that the paints can be easily processed using conventional by spraying, which can be applied to the surface to be coated.
• the solvent content of these paints causes problems, since technically complex measures have to be taken when processing the paints to ensure that the solvents that are released when the paints are applied and dried do not get into the atmosphere.
• the objects provided with the coating agents should be curable by irradiation with UN radiation.
• the hardness should increase suddenly after short exposure to relatively low radiation doses, without prolonged exposure causing a noticeable increase in hardness would.
• this hardening can only be achieved with very high radiation doses, ie the required dwell times in the existing radiation systems are still too long. Systems are therefore required which have groups which, under the action of radiation, react virtually quantitatively in a polymerization reaction with the lowest possible radiation doses, ie short exposure times.
• processors are increasingly demanding dual systems. These systems are characterized in that they are both radiation-curable and curable by a second, independent curing mechanism. Systems which can be precured to a film which is dry from dust by applying the coating agent for as short a time as possible are particularly desired. This film should then cure further in the course of a few days by simply storing it in air at room temperature or with heating until a hard film has formed which has the final desired properties.
• This type of two-stage curing is of particular importance because it enables the processors of the coating agent systems to coat an object with a film in a first step and to further process this film in a second step, in particular the already coated article after To give radiation a specific profile using pressure.
• the films or foils must therefore have already hardened when they are deformed in the second working step, so that they do not stick to the tools during the deformation, but on the other hand they must not yet be so hard that they tear when stretched and deformed.
• the coated articles produced in this way must then be stored for a while until the coating has reached its final use properties.
• substrates pre-coated with primers, fillers, color effect layers or other coatings as well as directly on plastics, wood, wood-based materials, paper, glass, ceramics, textiles, leather or metal.
• EP-A-549116 and DE-A-3819627 relate to compounds which contain both isocyanate groups and free-radically polymerizable C-C double bonds. These compounds are prepared by dimerizing or trimerizing commercially available aliphatic isocyanates to those containing uretdione, isocyanurate or biuret groups and then reacting them with hydroxyalkyl acrylates. A disadvantage of these systems is that they have a very high viscosity and processing can only be carried out with the addition of large amounts of solvent.
• US Pat. No. 5,739,251 also discloses urethanes from alcohols containing beta, gamma-ethylenically unsaturated ether groups which are practically free from isocyanate groups, and allophanates derived from these urethanes.
• the aforementioned beta, gamma-unsaturated compounds have the particular disadvantage that they have a high viscosity act and are not themselves radiation-curable.
• the present invention is therefore based on the object of providing compounds with which coating agent systems can be produced which have the aforementioned requirement profile with regard to the processing and use properties.
• the coating agent systems should have a low viscosity with a low solvent content and be usable as dual systems, in which radiation curing can be carried out completely with lower radiation doses (or until the films are tack-free or scratch-resistant).
• the compounds I according to the invention are generally essentially free of uretdione, biuret or isocyanurate groups.
• Preferred compounds I are thus those of the general formula I.
• n is an integer from 1 to 10, preferably 1 to 5
• R 1 is a divalent aliphatic or alicyclic C to C 0 hydrocarbon unit or an aromatic C 5 to C 20 hydrocarbon unit R 2 in each repeating unit once for -NH- and once for NC (0) -R 3 , where R 3 stands for a residue derived from an alcohol by abstraction of the H atom from the alcoholic hydroxyl group, the alcohol as functional groups bearing an activated double bond in addition to the alcohol group.
• the radicals R 1 are preferably those which are derived from conventional aliphatic or aromatic polyisocyanates by abstraction of the isocyanate group.
• the diisocyanates are preferably aliphatic isocyanates with 4 to 20 carbon atoms.
• Examples of customary diisocyanates are aliphatic diisocyanates such as tetramethylene diisocyanate, hexamethylene diisoeyanate (1,6-diisocyanatohexane), octamethylene diisocyanate, decamethylene diisocyanate, dodecamethylene diisocyanate, tetradecamethylene diisocyanate, derivatives of lysine diisocyanate, trimethyl diisocyanate, tetra diisocyanate 4-, 1,3- or 1,2-diisocyanatocyclohexane, 4,4'- or 2,4'-di (iso- cyanatocyclohexyDmethane, l-
• the alcohols A from which the radical R 3 is derived are, for example, esters of ⁇ , ⁇ -unsaturated carboxylic acids, such as acrylic acid, methacrylic acid (hereinafter "(meth) acrylic acid”), crotonic acid, acrylamidoglycolic acid, Methacrylamidoglycolic acid or vinyl acetic acid and polyols with preferably 2 to 20 carbon atoms and at least 2 hydroxyl groups, such as ethylene glycol, diethylene glycol, triethylene glycol, 1, 2-propylene glycol, 1, 3-propylene glycol, dipropylene glycol, tripropylene glycol, 1,4-butanediol , 1, 5-pentanediol, neopentyl glycol, 1, 6-hexanediol, 2-methyl-l, 5-pentanediol, 2-ethyl-l, 4-butanediol, 1, 4-dimethylol-cyclohexane, gly
• radicals R 3 can also of the amides of (meth) acrylic acid with amino alcohols, for. B. 2-aminoethanol, 3-amino-l-propanol, l-amino-2-propanol or 2- (2-aminoethoxy) ethanol and the vinyl ethers of the aforementioned polyols, provided they still have a free OH group.
• Unsaturated polyether or polyesterols or polyacrylate polyols with an average OH functionality of 2 to 10 are also suitable as reactive components.
• the R 3 radicals are preferably derived from alcohols such as 2-hydroxyethyl (meth) acrylate, hydroxypropyl (meth) acrylate, 1,4-butanediol mono (meth) crylate, neopentylglycol mono (meth) acrylate, glycerol mono- and di (meth) acrylate, trimethylolpropane mono- and di (meth) acrylate, pentaerythritol di- and tri (meth) acrylate.
• alcohols such as 2-hydroxyethyl (meth) acrylate, hydroxypropyl (meth) acrylate, 1,4-butanediol mono (meth) crylate, neopentylglycol mono (meth) acrylate, glycerol mono- and di (meth) acrylate, trimethylolpropane mono- and di (meth) acrylate, pentaerythritol di- and
• Alcohol A is particularly preferably selected from 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, hydroxypropyl acrylate, 1,4-butanediol monoacrylate and 3- (acryloyloxy) -2-hydroxypropyl methacrylate.
• amides of ethylenically unsaturated carbon Acids with amino alcohols are hydroxyalkyl (meth) acrylamides such as N-hydroxymethylacrylamide, N-hydroxymethylmethacrylamide, N-hydroxyethylethylacrylamide, N-hydroxypropyl methacrylamide, 5-hydroxy-3-oxopentyl ⁇ meth) acrylamide, N-hydroxyalkylcrotonamides such as N-hydroxymethyl 5-acrylamide or N-hydroxyalkyl maleimides such as N-hydroxyethyl maleimide.
• the isocyanate groups of the compounds 1 can also be present in capped form. Suitable capping agents for NCO groups
• the compounds I are preferably used in the form of mixtures (mixtures I) containing
• a2) 0 to 99% by weight of another compound which, in addition to one or more isocyanate groups, is also a group selected from the group consisting of urethane, urea, biuret, 25 allophanate, carbodiimide, uretonimine, uretdione and Contains isocyanurate groups.
• Isocyanates which may be present in the mixtures I in addition to the compounds I, are aliphatic and aromatic diisocyanates and in particular higher-functionality polyisocyanates (polyisocyanates a2) from the following groups:
• the isocyanato isocyanurates generally have an NCO content of 10 to 30% by weight, in particular 15 to 25% by weight, and an average NCO functionality of 2.6 to 4.5.
• R 1 has the same meaning as in compounds of the formula I.
• diisocyanates containing uretdione groups with aromatic, aliphatic and / or cycloaliphatic isocyanate groups, preferably derived from hexamethylene diisocyanate or isophorone diisocyanate.
• Polyuretdione diisocyanates are dimerization products of the diisocyanates (isocyanates a2.2).
• Polyisocyanates containing biuret groups with aliphatic isocyanate groups in particular tris (6-isocyanatohexyDbiuret or its mixtures with its higher homologues.
• These polyisocyanates containing biuret groups generally have an NCO content of 10 to 30
• Polyisocyanates containing urethane and / or allophanate groups, with aliphatic or cycloaliphatic isocyanate groups which are free of radically polymerizable CC double bonds, the CC double bonds being linked directly to a carbonyl group or an O atom in ether function are activated i & t.
• Such compounds are obtainable, for example, by reacting excess amounts of hexamethylene diisocyanate or isophorone diisocyanate with mono- or polyvalent C 1 -C -monoalcohols, polyhydric alcohols such as ethylene glycol, trimethylolpropane, glycerol or mixtures thereof. These have urethane and / or allophanate groups
• Polyisocyanates generally have an NCO content of 12 to 25% by weight and an average NCO functionality of 2.5 to 4.5 (isocyanates a2.4)
• Polyisocyanates containing oxadiazinetrione groups preferably derived from hexamethylene diisocyanate or isophorone diisocyanate. Such polyisocyanates containing oxadiazinetrione groups can be prepared from diisocyanate and carbon dioxide. (Isocyanates a2.6)
• the isocyanate groups of the polyisocyanates (a2.1) to (a2.7) mentioned can also be partially reacted with monoalcohols.
• the content of activated double bonds of the compounds I is generally 0.002 to 20% by weight, and preferably 0.01 to 10% by weight.
• the content of isocyanate groups of components al and a2, based on the total amount of mixture components al and a2. is generally 0.1 to 40, and preferably 1 to 30 wt.%.
• a molar mass of 24 g / mol is used and when specifying the isocyanate content in% by weight, it is based on 42 g / mol.
• the ratio of the activated double bonds of the compounds I to the isocyanate groups of the mixture components a1 and a2 is generally 50: 1 to 0.02: 1 and preferably 10: 1 to 0.1: 1.
• Mixtures I which contain the components al and a2.1 to a2.7 in the following composition are particularly preferred:
• Component al 5 - 95% by weight component a2.1: 5 - 60% by weight component a2.5: 0 - 60% by weight
• the mixtures I usually have viscosities (measured at 23 ° C.) of less than 50,000 mPas, preferably from 100 to 30,000 mPas.
• the compounds I can be prepared by the polyisocyanates and the alcohols A, from which the compounds I are derived, at reaction temperatures of 0 to 280, preferably at 20 to 250 ° C., in the presence of a promoting allophanate formation Catalyst, for example an organic zinc compound such as zinc acetylacetonate or zinc 2-ethylcaproate, or a tetraalkylammonium compound such as N, N, N-trimethyl-N-2-hydroxypropylammonium hydroxide or such as N, N , N-trimethyl-N-2-hydroxypropylammonium-2-ethylhexanoate.
• a promoting allophanate formation Catalyst, for example an organic zinc compound such as zinc acetylacetonate or zinc 2-ethylcaproate, or a tetraalkylammonium compound such as N, N, N-trimethyl-N-2-hydroxypropylammonium hydroxide or such
• the amounts of the starting compounds are chosen so that the isocyanate groups are in excess.
• the molar ratio of the polyisocyanate used to the alcohol A used is generally 1: 1 to 30: 1, preferably 1.5: 1 to 20: 1.
• polymerization inhibitors are added to the reaction.
• These are the usual compounds suitable for hindering free-radical polymerization, e.g. B. hydroquinones or hydroquinone monoalkyl ether, 2,6-di-tert-butylphenols, such as 2,6-di-tert-butylcresol, nitrosamines, phenothiazines or phosphorous acid esters.
• the reaction can be carried out either without a solvent or with the addition of solvents.
• Inert solvents e.g. B. acetone, methyl ethyl ketone, tetrahydrofuran, dichloromethane, toluene, -C -C alkyl esters of acetic acid such as ethyl acetate or butyl acetate.
• the reaction is preferably carried out without solvent.
• the corresponding isocyanates a2.5 and, from this, the compounds I with an allophanate group are formed during the reaction. These can extend to compounds with more than one allophanate group, for example the compounds of the formula I in which n is greater than 1.
• the progress of the reaction is expediently followed by gel permeation chromatography (GPC) or by determining the NCO content of the reaction mixture.
• GPC gel permeation chromatography
• the reaction can be stopped by adding deactivators. Suitable deactivators are, for example, inorganic or organic acids, the corresponding acid halides and
• Alkylating agent examples include phosphoric acid, mono-chloroacetic acid, dodecylbenzenesulfonic acid, benzoyl chloride, dimethyl sulfate and preferably dibutyl phosphate and di-2-ethylhexyl phosphate.
• the deactivating agents can be used in amounts of 1 to 200 mol%, preferably 20 to 150 mol%, based on the moles of catalyst. In most cases, any remaining residues of unconverted are left after the implementation has ended Polyisocyanate is distilled off in vacuo to a content of less than 0.5%.
• reaction is usually stopped when the reaction mixture has the following composition, provided that any amounts of polyisocyanate still present are disregarded:
• Compound I with 1 allophanate group 1 to 100, preferably 5 to 80% by weight,
• the compounds I can be isolated from the reaction mixtures using customary separation methods, e.g. with the help of gel permeation chromatography. In most cases, however, this is not necessary, since the by-products are also valuable products which can usually be present in coating agent systems which contain the compounds I.
• the compounds I or mixtures I can be cured, on the one hand, by irradiation with high-energy radiation, if appropriate in the presence of other radically polymerizable compounds having C-C double bonds, the C-C double bonds of the compounds I and, if appropriate, the other free-radically polymerizable compounds being polymerized.
• the compounds I or mixtures I can be cured by reaction of the isocyanate groups in a polyaddition reaction (hereinafter referred to as "isocyanate curing"), e.g. by adding compounds I or mixtures I, prior to their use, which contain at least one group which is reactive toward isocyanate, which reacts with the isocyanate groups in an addition reaction, or by diffusing such compounds into a coating of compounds I or mixtures I from a gaseous medium leaves.
• isocyanate curing e.g. by adding compounds I or mixtures I, prior to their use, which contain at least one group which is reactive toward isocyanate, which reacts with the isocyanate groups in an addition reaction, or by diffusing such compounds into a coating of compounds I or mixtures I from a gaseous medium leaves.
• Isocyanate curing can be accelerated by increasing the temperature. Temperatures of up to 130 ° C. are generally suitable for this, since at these temperatures it is possible to effect only isocyanate curing without the polymerization of the C-C double bond commencing.
• the compounds or mixtures I can already be used without additional additives as coating agents and especially as dual systems, because films of these coating agents can be cured both with the aid of high-energy radiation, optionally with the addition of photoinitiators, and by means of isocyanate curing.
• Isocyanate curing of the coatings can also e.g. in contact with a medium which contains a substance (W) which is reactive toward isocyanate groups.
• substance (W) in the form of a gas from the ambient atmosphere, or a liquid or a substance which is applied, for example, to a solid carrier material can act on films of the coating compositions. Examples would be water vapor, ammonia or amines, which are absorbed and react from the gas phase.
• Substances (W) which act from condensed phases such as in the case of water, alcohols, amines and their solutions, are also suitable.
• Coated substrates can also harden, for example, by immersing them in liquids or wetting them with liquids which contain the substances (W) in the immersed state or in the state wetted with liquid substance (W).
• the substrates are preferably radiation-hardened before dipping to avoid bubbles which can be formed in the reaction. Avoiding the formation of bubbles in isocyanate reactions with water by radiation is a further advantage of the invention.
• the reactive substances (W) can also be found on carrier materials.
• moist substrates such as wood, paper, foams, mineral carriers, which can then be coated directly with the compounds or mixtures I and, for example, undergo a further curing reaction after exposure to UN radiation.
• moist substrates especially wood or mineral substrates e.g. Concrete form panels or fiber cement panels possible without predrying the substrate.
• moist substrates especially wood or mineral substrates e.g. Concrete form panels or fiber cement panels possible without predrying the substrate.
• the compounds I and mixtures I are mostly used in the form of radiation-curable preparations which contain the customary auxiliaries, that is to say, for example. Nerdicker, defoamers, leveling agents, dyes, fillers or pigments and, if necessary, photoinitiators and stabilizers (hereinafter briefly: “preparations S").
• a variant of the invention are preparations S which are identical to each other.
• the compounds S are often so-called reactive diluents or binders, as described, for example, in "Chemistry & Technology of UV & EB Formulations for Coatings, Inks & Paints, Vol. 1-5, Ed. PKT Oldring, London 1991, are mentioned.
• Suitable reactive diluents are, for example, vinyl group-containing monomers, in particular N-vinyl compounds, such as N-vinylpyrrolidone, N-vinylcaprolactam and N-vinylformamide, and also vinyl ethers, such as ethyl, propyl, isopropyl, butyl, isobutyl, tert .
• N-vinyl compounds such as N-vinylpyrrolidone, N-vinylcaprolactam and N-vinylformamide
• vinyl ethers such as ethyl, propyl, isopropyl, butyl, isobutyl, tert .
• Preferred reactive diluents are mono- or polyfunctional esters of alpha, beta-ethylenically unsaturated carboxylic acids with aliphatic mono- or polyols.
• suitable polyol components are the above-mentioned diols or polyols which have been mentioned in connection with alcohols A.
• Examples of monools are conventional alcohols or their alkoxylation products with ethylene oxide or propylene oxide, for example methanol, ethanol, ethylhexanol, tertiary-butylcyclohexanol, tetrahhydrofurfuryl alcohol, norbornyl alcohol, lauryl alcohol, stearyl alcohol, phenoxyethyl glycol, methoxytroxytriphtylene glycol, methoxytroxytripethylene glycol.
• the polyalcohols can be complete or incomplete of the alcohol groups per molecule must be esterified with the alpha, beta-ethylenically unsaturated carboxylic acids.
• reactive diluents examples include tertiary-butylcyclohexanolacrylate, tetrahhydrofurfurylacrylate, norbornyl acrylate, laurylacrylate, stearyl acrylate, phenoxyethylglycol acrylate, methoxytriethylene glycol acrylate, methoxytripropylene glycol acrylate (XXX) acrylic (meth) acrylate (XXX) monoglycol, ethylene (meth) acrylate, methylene glycol, ethylene (meth) acrylate, methacrylate and methacrylate (XXX) monoalkylene glycol, methacrylate methacrylate, - Koldi (meth) acrylate, propylene glycol (meth) acrylate, butylene glycol di (meth) acrylate, butylene glycol (meth) acrylate, 1,6-hexanediol di (meth) acrylate,
• esters of ethoxylated polyols e.g. B. the polyacrylates or methacrylates of alkoxylated trimethylolpropane, alkoxylated ditrimethylolpropane, glycerol, pentaerythritol or dipentaerythritol.
• the binders with free-radically polymerizable CC double bond are prepolymers, polymers or oligomers, preferably up to molecular weights of 10,000 such as (meth) acrylic functional (meth) acrylic copolymers, epoxy (meth) acrylates, polyester (meth ) acrylates, polyurethane (meth) acrylates, polyethers (methacrylates, silicon (meth) acrylates, melamine (meth) acrylates, unsaturated polyesters with maleic acid groups, unsaturated polyurethanes with maleic acid groups.
• (meth) acrylic functional (meth) acrylic copolymers epoxy (meth) acrylates, polyester (meth ) acrylates, polyurethane (meth) acrylates, polyethers (methacrylates, silicon (meth) acrylates, melamine (meth) acrylates, unsaturated polyesters with maleic acid groups, unsaturated polyurethanes with maleic acid groups.
• a large number of the binders mentioned can have groups which are reactive toward isocyanate, in particular hydroxyl groups which e.g. incompletely esterified polyols or in the form of ⁇ -hydroxy (meth) acrylate groups in epoxy acrylates. Additional binders containing hydroxyl groups are addition products of components containing isocyanate groups with excess polyols. This affects viscosity, pot life and dual your properties.
• All compounds S can also contain amine groups up to an amine number of 250 mg KOH / g, for example by adding primary or secondary amines to double bonds.
• Such amines are preferred wise aliphatic amines such as methylamine, dimethylamine, ethylamine, diethylamine, propylamine, dipropylamine, butylamine, dibutylamine, and hydroxyaliphatic amines such as ethanolamine, diethanolamine, propanolamine and dipropanolamine.
• the binders and reactive diluents can be used individually or in a mixture.
• Suitable fillers include silicates, e.g. B. by hydrolysis of silicon tetrachloride available silicates such as Aerosil® from Degussa, silica, talc, aluminum silicates, magnesium silicates, calcium carbonates etc.
• Suitable stabilizers include typical UN absorbers such as oxanilides, triazines and benzotriazole (the latter available as Tinuvin® R brands Ciba Specialty Chemistry) and Benzophenone. These can be used alone or together with suitable free radical scavengers, for example sterically hindered amines such as 2, 2, 6, 6-tetramethylpiperidine, 2, 6-di-tert-butylpiperidine or their derivatives, e.g. B. bis- (2, 2, 6, 6-tetra-methyl-4-piperidyl) sebacinate can be used.
• Stabilizers are usually used in amounts of 0.1 to 5.0% by weight, based on the components contained in the preparation with activated double bonds
• the preparations according to the invention contain at least one photoinitiator which can initiate the polymerization of ethylenically unsaturated double bonds.
• photoinitiator which can initiate the polymerization of ethylenically unsaturated double bonds.
• photoinitiator which can initiate the polymerization of ethylenically unsaturated double bonds.
• These include benzophenone and benzophenone derivatives, such as 4-phenylbenzophenone and 4-chlorobenzophenone, Michler's ketone, acetophenone derivatives, such as 1-benzoylcyclohexan-1-ol, 2-hydroxy-2, 2-dimethylacetophenone and 2,2-dimethoxy -2-phenylacetophenone, benzoin and benzoin ethers, such as methyl, ethyl and butyl benzoin ethers, benzil ketals, such as benzil dimethyl ketal, 2-methyl-l- [4- (methylthio)
• the abovementioned photoinitiators are used in amounts of 0.05 to 20% by weight, preferably 0.1 to 10% by weight and in particular 0.2 to 5% by weight, based on the compounds I and S of the preparations according to the invention are used.
• Amines can be added as coinitiators to improve the curing rate.
• Such amines are usually compounds such as tributylamine, triethanolamine, dimethylethanolamine, methyldiethanolamine. These are used in amounts of 1 to 10% by weight based on the paint solids.
• binders containing amino groups such as, for example, by adding aliphatic or hydroxyaliphatic primary or secondary amines, such as methylamine, dimethylamine, ethylamine, diethylamine, propylamine, dipropylamine, butylamine, dibutylamine, ethanolamine, diethanolamine, propanolamine and dipropanolamine to acrylic ester monomers and of the acrylic ester monomer type Connections S can be produced.
• aliphatic or hydroxyaliphatic primary or secondary amines such as methylamine, dimethylamine, ethylamine, diethylamine, propylamine, dipropylamine, butylamine, dibutylamine, ethanolamine, diethanolamine, propanolamine and dipropanolamine
• Such amine-modified products can also serve as main binders and up to 98% by weight of formulation can be used.
• photoinitiators can be dispensed with.
• the preparations according to the invention can also contain pigments.
• 2-component coating compositions are prepared from the preparations S by adding a compound having groups which are reactive toward isocyanate groups (hereinafter “compounds R") to the preparations S before processing.
• compounds R a compound having groups which are reactive toward isocyanate groups
• the mixing of the two components is expediently carried out at most 24 hours before the coating agent is applied to the object to be coated.
• the ratio of the isocyanate groups to the groups reactive toward isocyanate groups is usually 2: 1 to 0.5: 1, preferably 10: 1 to 0.7: 1, particularly preferably 0.9: 1 to 1.1: 1.
• the compounds R are generally those which are present as the A component in customary 2-component polyurethane coating compositions, that is to say, for example, low molecular weight alcohols having 2 to 20 C atoms and 2 to 6 OH Groups or hydroxy-functional polymers (hereinafter "polymers (A)").
• the polymers (A) are as • are polymers having a hydroxyl group content of 0.1 to 20, preferably 0.5 to 10 % By weight.
• the number average molecular weight M n of the polymer is preferably 1000 to 100000, particularly preferably 2000 to 10 000.
• the polymers are preferably those composed of more than 50 wt .-% of C _, - to C o alkyl ( meth) acrylate, 5 vinyl aromatics with up to 20 C atoms, vinyl esters of up to 20 C atoms containing carboxylic acids, vinyl halides, non-aromatic hydrocarbons with 4 to 8 C atoms and 1 or 2 double bonds, unsaturated nitriles and mixtures thereof.
• Particularly preferred are the polymers which consist of more than 10 60 wt .-% of -C ⁇ to Cio-alkyl (meth) acrylates, styrene or mixtures thereof.
• the polymers (A) contain hydroxy-functional monomers corresponding to the above hydroxyl group content and, if appropriate, further monomers, e.g. ethylenically unsaturated acids, especially carboxylic acids, acid anhydrides or acid amides.
• polyesterols as can be obtained by condensing polycarboxylic acids, in particular dicarboxylic acids, with polyols, in particular diols.
• polymers (A) are also polyetherols which are prepared by adding ethylene oxide, propylene oxide or butylene oxide to 25 H-active components. Polycondensates made from butanediol are also suitable.
• the polymers (A) can of course also be compounds with primary of the secondary amino groups.
• Coating agents are suitable as coating
• the preparations according to the invention prove to be particularly suitable for coating substrates such as wood, wood-based materials, paper, textile, leather, fleece, plastic surfaces, glass, ceramics, mineral building materials such as shaped cement blocks and fiber cement boards, and in particular metals or corresponding precoated substrates.
• substrates such as wood, wood-based materials, paper, textile, leather, fleece, plastic surfaces, glass, ceramics, mineral building materials such as shaped cement blocks and fiber cement boards, and in particular metals or corresponding precoated substrates.
• the present invention also relates to a method for coating substrates, in particular metals or coated metals, such as those e.g. can also be used in the vehicle body or coil coating area, as well as the coated substrates obtainable by this process.
• the substrates are generally coated by applying at least one radiation-curable preparation according to the invention to the substrate to be coated in the desired thickness and removing any solvent which may be present. If desired, this process can be repeated one or more times.
• the radiation-curable preparations are applied to the substrate in a known manner, e.g. B. by dipping, spraying, filling, knife coating, brushing, rolling, rolling or pouring.
• Films coated according to the invention e.g. Paper or plastic can also be laminated, if necessary with the help of an adhesive.
• the adhesive can be applied both to the coated films and to the substrate.
• the films, which are either partially photochemically or thermally hardened, can be deformed before, during or after application. This enables film coatings on non-planar substrates or the deformation of the coated substrates.
• the coating thickness is generally in the range from 3 to 3000 g / m 2 and preferably 10 to 2900 g / m 2 .
• the coatings are then cured both by irradiation with high-energy radiation and by adding the isocyanate groups with atmospheric moisture or
• isocyanate curing In contrast to radiation curing, which takes place within a few seconds or fractions of a second, isocyanate curing usually proceeds slowly, i.e. at room temperature it is often only completed after days. However, it can also be accelerated by selecting suitable catalysts, at elevated temperature, preferably up to 200 ° C., or by adding suitable reactive reactants. At curing temperatures above
• the reactive double bonds can also react without the addition of thermal initiators and contribute to curing, so that additional radiation can be dispensed with. Curing temperatures for the polymerization of the double bonds without irradiation can be achieved by adding thermally radical-forming polymers.
• risk initiators such as organic peroxide or azo compounds, if appropriate in combination with accelerators based on cobalt compounds or amines, can be reduced to below room temperature.
• Radiation curing takes place by the action of high-energy radiation, that is to say UN radiation or daylight, preferably light of the wavelength 250 to 600 nm, or by irradiation with high-energy electrons (electron radiation; 150 to 300 keV).
• high-energy radiation that is to say UN radiation or daylight, preferably light of the wavelength 250 to 600 nm, or by irradiation with high-energy electrons (electron radiation; 150 to 300 keV).
• High-pressure mercury vapor lamps, lasers, pulsed lamps (flashing light), halogen lamps or 30 excimer lamps are used as radiation sources.
• the radiation dose usually sufficient for crosslinking with UN curing is in the range from 80 to 3000 mJ / cm 2 .
• coatings can also cure under light sources similar to daylight or in sunlight.
• the irradiation can optionally also be carried out with the exclusion of oxygen, e.g. B. under an inert gas atmosphere, or under atmospheres with reduced oxygen contents below 17 wt .-%.
• Suitable inert gases are preferably nitrogen, noble gases, carbon dioxide, or combustion gases.
• Irradiation can also be carried out by covering the coating material with transparent media.
• Transparent media are, for example, plastic films, glass or liquid like water.
• curing takes place continuously by moving the substrate treated with the preparation according to the invention past a radiation source at a constant speed. For this it is necessary that the curing speed of the preparation according to the invention is sufficiently high.
• This different time course of hardening can be used in particular if the coating of the object is followed by a processing step in which the film surface comes into direct contact with another object or is mechanically processed.
• step Ia coated an object with a film of the coating agent, Ha. in step Ha the film of the coating agent is irradiated with high-energy radiation, the film being pre-hardened, purple, in step purple the object which is coated with the pre-hardened film of the coating agent is processed, in particular deformed, covered with a further or more coatings or brings the surface of the pre-cured film into contact with another object and IVa. in step IVa, the precured film of the coating composition with which the processed object is coated is finally cured by isocyanate curing.
• step Ib coated an object with a film of the coating composition
• step Ib coated an object with a film of the coating composition
• step IIb precuring the film of the coating composition with which the object is coated by allowing the isocyanate groups to react in a polyaddition reaction
• step IIIb the object which is coated with the precured film of the coating agent is processed, in particular deformed, covered with another or more coatings or the surface of the precured film is brought into contact with another object and IVb.
• step IVb the pre-cured film of the coating agent is irradiated with high-energy radiation, the film being finally cured.
• the advantage of this method is that the coated articles can be processed immediately after step Ha or Ilb, because the surface can be made tack-free or sticky.
• the pre-cured film is so flexible and stretchable that the article can be deformed without the film flaking or tearing.
• direct mechanical processing such as shaping or sanding is particularly possible without sticking the sanding paper.
• the so-called dual your method can prove to be advantageous, because the objects provided with the pre-hardened film can be transported and stored particularly easily, e.g. in stacks.
• the dual your method offers the advantage that the coating compounds can be chemically cured in dark areas (areas that are not accessible to the radiation) and thus sufficient material properties can be achieved regardless of the radiation.
• spray mist harden - precipitation free of tack and emissions This makes these coating compositions particularly suitable for use as sealing compounds with rapid curing in illuminable areas and post-curing in dark areas.
• step IVa is often carried out in such a way that the coated articles are stored in air for a few more days at room temperature or elevated temperature in order to accelerate the curing process.
• the isocyanate groups react with air humidity or possibly the A component, increasing the network density and giving the film its final properties.
• the compounds I, mixtures I or a preparation S are in particular in the form of casting resin, filler, sealing compound, solder resist, photoresist resin, stereolithography resin, printing ink, adhesive, dental compound, for producing photopolymer printing plate.
• a relief can be produced in a washing-out process downstream of the imaging radiation curing with solvents or aqueous washing liquids.
• Thermal post-curing of the photopolymerized materials gives higher mechanical and chemical resistance, which is necessary for use e.g. as a pressure plate, printed circuit board or as another molded part.
• Hexamethylene diisocyanate (HDI) was placed under a blanket of nitrogen and the amount of stabilized OH component stated in Table 1 was added.
• the mixture was heated to 80 ° C. and 200 ppm by weight (based on diisocyanate) of the catalyst N, N, N-trimethyl-N- (2-hydroxypropyl) ammonium 2-ethylhexanoate were added.
• the temperature slowly increased to 120 ° C.
• the reaction was allowed to take place at this temperature and the reaction was stopped at the NCO content of the mixture given in Table 1 by adding 250 wt. Ppm (based on diisocyanate) of di-2- (ethylhexyl) phosphate.
• the reaction mixture was then freed of unreacted HDI in a thin film evaporator at 135 ° C. and 2.5 mbar.
• Hexamethylene diisocyanate (HDI) was initially introduced under a blanket of nitrogen and the amount of stabilized 3- (acryloyloxy) -2-hydroxypropyl methacrylate stated in Table 1 was added.
• the mixture was heated to 80 ° C. and 500 wt. Ppm (based on diisocyanate) of the catalyst zinc acetylacetonate were added.
• the temperature was then slowly increased to 120 ° C. You let react at this temperature and stopped the reaction at the NCO content of the mixture given in Table 1 by adding 550 wt. ppm (based on diisocyanate) di-2- (ethyl-hexyl) phosphate.
• the reaction mixture was then freed of unreacted HDI in a thin-layer evaporator at 135 ° C. and 2.5 mbar.
• the diisocyanates were placed under a blanket of nitrogen and the amount of stabilized OH component stated in Table 1 was added.
• the mixture was heated to 100 ° C. and 200 ppm by weight (based on diisocyanate) of the catalyst N, N, N-trimethyl-N- (2-hydroxypropyl) ammonium 2-ethylhexanoate were added.
• the temperature slowly increased to 120 ° C.
• the reaction was allowed to take place at this temperature and the reaction was stopped at the NCO content of the mixture given in Table 1 by adding 250 wt. Ppm (based on diisocyanate) of di-2- (ethylhexyl) phosphate.
• the reaction mixture was then freed of unreacted isocyanate in a thin film evaporator at 135 ° C. and 2.5 mbar.
• HDI polyisocyanate having an average functionality of about 3.5 and an NCO content of 22.0 wt.% (BASONAT ® HI 100, BASF AG) were inserted superiors under nitrogen blanketing, dibutyltin dilaurate added with 200 ppm and heated to 55 ° C. The amounts of hydroxyethyl acrylate (stabilized) given in Table 2 were added over the course of 15 minutes and the batch was slowly warmed to 80 ° C. The mixture was then stirred at 80 ° C for one hour.
• BASONAT ® HI 100 BASF AG
• HDI hexamethylene diisocyanate
• IPDI isophorone diisocyanate
• 1,3-BIC 1,3-bis (isocyanatomethyl) cyclohexane
• HEA hydroxyethyl acrylate
• HPA hydroxypropyl acrylate
• HEMA hydroxyethyl methacrylate
• GAMA 3- (acryloyloxy) -2-hydroxypropyl methacrylate
• the products or comparative products according to the invention were, if they had a viscosity of more than 500 mPas, diluted to 500 mPas with butyl acetate (BuAc).
• the samples were drawn onto glass or sheet metal using film drawing frames.
• the films which are optionally vented from the solvent at room temperature, are irradiated 5 times at 10 m / min belt speed under an IST high-pressure mercury lamp (120 W / cm).
• the films are stored for several days at room temperature and 50% humidity.
• Table 3 describes the result after curing only with air humidity
• Table 4 describes the result after curing with air humidity and UN curing
• Pendulum damping lacquer on glass as substrate (DI ⁇ 53157) with a lacquer layer thickness, dry, of approx. 30 ⁇ m in the case of air hardening and approx. 50 ⁇ m in the case of UN hardening.
• Product No. 6 according to the invention was mixed 0 with the hydroxifunctional vinyl polymer (Lumitol® H 136, BASF) on the one hand according to the stoichiometric OH / NCO ratio and on the other hand in the same proportions for the comparison test.
• a clear lacquer based on the same acrylate resin in combination with the polyisocyanate hardener (Basonat® P LR 8901, BASF) was tested.
• the setting to an application viscosity of 20 s (DIN 53 211 cup 4 mm outlet nozzle) was carried out with butyl acetate.
• the films which have been vented from the solvent at room temperature are irradiated 9 times at a belt speed of 15 m / min under an IST high-pressure mercury lamp (120W / cm).
• V2 was produced according to the information in EP 549 116, the products V3 and V4 were designed for a higher double bond content.
• Kl 50 parts of an allophanate adduct from HEA and HDI with 12.1% NCO and a viscosity of lPas with the auxiliary system from IT part of a 1% dibutyltin dilaurate solution in butyl acetate, 2 parts of a mixture of Irgacure 184 (Ciba specialty chemicals) and 0.5 parts of lucirin TPO (BASF AG) (ratio 8.75: 1.25), 0.5 part Tinuvin 292 (Ciba S.) and 0.75 part Tinuvin 400 (Ciba S.) are applied to a glass plate with a layer thickness of 50 ⁇ m. The film is irradiated twice under a UV mercury high-pressure lamp (120W / cm) at a belt speed of 5 m / min. The mixture is then heated at 130 ° C for 30 minutes.
• a UV mercury high-pressure lamp 120W / cm
• a sponge covered with silicon carbide is moved over the cooled paint film under the load of a 500g hammer.
• the loss of gloss measured at 60 ° after a different number of strokes was determined as a measure of the scratch sensitivity.
• K2 Analogously to C1, a film was produced and tested from 44.7 parts of the allophanate acrylate with 6.54 parts of 1,2-propanediol and the auxiliary system from 1).
• K3 Analogously to C1), a film was produced from 39.4 parts of the allophanate acrylate with 10.6 parts of a polyetherol from the adduct of 1 mol of trimethylolpropane with 3 mol of ethylene oxide (Lupranol VP 9236) and the auxiliary system from 1) and tested.
• a solvent-containing two-component polyurethane paint (2K PU) from automotive serial painting (BASF Coatings AG) was used as a comparison, which was baked analogously at 130 ° / 30 minutes.
• the isocyanato acrylate paints show a significantly lower loss of gloss and thus a higher scratch resistance. They are suitable for automotive painting.
• Example Kl has the additional advantage of being processable as a one-component lacquer.
• Lacquer 1 (comparison) 60 parts polyester acrylate (Laromer PE 56F) 40 parts tripropylene glycol diacrylate (TPGDA) 4 parts Irgacure 184 (photo initiator of
• Ciba Specialty Chemicals 1 part benzophenone 1 part CAB 551-001 (cellulose acetobutyrate from Kodak) Viscosity: 1.2 Pas
• Lacquer 1 is applied as a primer at 26 g / m2 on beech veneer and UV-cured at 10 m / min, then another 24 g / m2 is applied and finally cured at 5 m / min with UV.
• 15 cm 2 of the coated veneer are crushed and extracted with 10 ml of methylene chloride (covering) in a Duran ampoule at 40 ° C. for 1 h.
• TPGDA of extractable acrylate components was determined by GC / MS to be 1330 mg / m2 veneer.
• Lacquer 2 100 parts of allophanate adduct made of HDI and HEA
• Lacquer 2 is applied as a primer with 25 g / m2 on beech veneer and UN-hardened at 2 m / min to a non-tacky layer, then 23 g / m2 of lacquer 1 is applied and UV-hardened twice at 2 m / min.
• Extractable proportions of acrylates are below the detection limit ( ⁇ 10 mg / m2).
• Lacquer2 (see K2) is applied to cherry veneer at 80g / m2 and UV-cured twice at 2m / min.
• the veneer is pressed onto a profiled carrier with a glue resin film at 120 ° C 100 kp / cm2 with a profiled counter mold.
• the deformability of the lacquer layer is sufficient for the deformation of the veneer and only tears when the veneer is damaged.
• the lacquer is poured into a polyethylene bowl to form a 3 mm high film. Curing is carried out with exclusion of light for 1 hour at room temperature and 30 min at 60 ° C and for 24 hours Stored at room temperature. The result is an elastomeric, transparent and bubble-free thick film that does not produce bubbles and does not flow even when heated to 130 ° C. After UV irradiation at 2 * 5 m / min belt speed under a 120 W / cm mercury high pressure lamp, the elastomer film hardens to a highly resistant, transparent thermoset body.
• the film surface hardens without the formation of surface defects, but these occur if the film is irradiated immediately after application without heating.
• the red pigmented lacquer of the last example but with the photoinitiator portion of the above example significantly reduced to 0.25 part, is applied to a thermoformable polypropylene film in a thickness of 50 ⁇ m and heated at 80 ° C. for 15 minutes.
• This film composite can be pulled and pressed onto a non-planar surface, eg a table top corner, without wrinkles.
• the thermoformability is retained if the film is stored protected from light.
• an additional layer of adhesive can be used either on the substrate or on the paint film or on both sides. After UV irradiation at a belt speed of 10 m / min under a 120 W / cm high-pressure mercury lamp, the film surface hardens to a highly resistant, weatherproof and scratch-resistant coating.
• a further improvement, above all with regard to the visual appearance and resistance properties, is achieved if a clear lacquer according to the example for the production of thick-layer deformable and post-hardenable films is additionally applied between the polypropylene film and the color layer as the deformable top coat layer.

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• 1998
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