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
  • 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
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
  • C08F283/006—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polymers provided for in C08G18/00
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
  • C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
  • C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
  • C08F290/06—Polymers provided for in subclass C08G
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
  • C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
  • C08F290/06—Polymers provided for in subclass C08G
  • C08F290/067—Polyurethanes; Polyureas
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F8/00—Chemical modification by after-treatment
  • C08F8/30—Introducing nitrogen atoms or nitrogen-containing 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
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/62—Polymers of compounds having carbon-to-carbon double bonds
  • C08G18/6216—Polymers of alpha-beta ethylenically unsaturated carboxylic acids or of derivatives thereof
  • C08G18/622—Polymers of esters of alpha-beta ethylenically unsaturated carboxylic acids
  • C08G18/6225—Polymers of esters of acrylic or methacrylic acid
  • C08G18/6229—Polymers of hydroxy groups containing esters of acrylic or methacrylic acid with aliphatic polyalcohols
• • 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
  • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
  • C09D133/04—Homopolymers or copolymers of esters
  • C09D133/14—Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen

Definitions

• the invention relates to synthetic resins based on poly (meth) aGrylat-urethane (meth) acrylates in urethane (meth) acrylates and optionally (meth) acrylates and / or reactive diluents and their preparation. Because of the reactive ethylenic groups, in particular in the side chains of the poly (meth) acrylate urethane (meth) acrylates, the synthetic resins according to the invention are free-radically curable and can be used as binders for mixtures of substances. The invention also relates to the composite materials and workpieces obtained from these mixtures, and to the production and use of these binders, composite materials and workpieces themselves. Furthermore, the synthetic resins according to the invention can also be used for the production of paints.
• Composites or composite materials are materials that are obtained by combining different materials and whose chemical and physical properties exceed those of the individual components.
• the most common production route for composites is the mechanical-thermal joining of one or more intercalated substances with a matrix.
• An alternative to mechanical-thermal joining consists in producing the constituents of the composite by phase separation from a homogeneous starting material. According to the current state of the art, only the mechanical-thermal joining is suitable for the production of large components and for mass production at low cost. The process route via phase separation is suitable for the production of small highly respected components, where the manufacturing costs are not so significant.
• GRP glass fiber reinforced plastics
• Polymer concrete a typical particulate composite material
• synthetic resins are basically constituted by the invention
• Synthetic resins could be replaced, serving as a matrix. So is in polymer concrete to
• inorganic fillers is usually an indirect bond via adhesion promoter, so are inorganic fillers z. B. often silanized.
• direct bonding via physicochemical bonding can occur when a polymeric filler is solubilized by the matrix monomer.
• This solubilization process takes place in the case of casting resins based on methyl methacrylate (MMA) / polymethyl methacrylate (PMMA).
• MMA methyl methacrylate
• PMMA polymethyl methacrylate
• MMA methyl methacrylate
• these systems which usually consist of at least two components, a liquid, the MMA with additives, and a powder containing PMMA with additives. If the methyl methacrylate component is then mixed with the polymethyl methacrylate component, the liquid dissolves the powder and a dough forms, which, depending on the particle size and molecular weight of the PMMA beads, becomes more or less rapid to a paste or highly viscous solution.
• This dissolution process is interrupted at the start of a polymerization reaction.
• the resulting here from the MMA new thread molecules penetrate the filler added as PMMA powder particles and entangle firmly with the thread molecules, so that initially a physical anchoring occurs.
• a direct bond is formed via chemical bonding when the matrix monomer can react with the filler polymer through a grafting reaction.
• grafting reactions are possible if the filler polymer, for example, still has unsaturated double bonds or other reactive functional groups, for example hydroperoxide, arnino or carboxyl groups, on its surface.
• the reaction of the monomers to polymers is always associated with a more or less strong volume contraction, also called shrinkage or shrinkage. This is due to the fact that the larger intermolecular distances between the monomer building blocks are replaced by the much shorter distances of the covalent bonds in the polymer chains.
• hardening reduces entropy and free volume. In principle, with increasing molecular weight of the monomers and increasing space requirements of the side chains and a decreasing proportion of reactive groups per monomer, the volume contraction is reduced.
• the hardening deliberately aims at the accumulation of fillers on the surface, so that it is less susceptible to scratching and heat, and often also to achieve optical effects. If such surfaces are polished to obtain specular surfaces, surface fillers will rotate at temperatures above the glass transition temperature of the particular polymethacrylate, thus reducing the stresses generated during curing, and provide a minimum in-line resistance Mirror effect disturbed surface.
• Examples of such resins which, as unsaturated compounds with reactive groups via free radicals, result in crosslinking reactions for film formation are, inter alia acrylated polyesters, acrylated urethanes, acrylated polyacrylates, acrylated epoxy resins, oligoether acrylates and unsaturated polyester / styrene binders.
• Urethane (meth) acrylates are used because of their high abrasion resistance and flexibility especially for the overcoating of PVC and Korkfspiböden. Further areas of application are wood coatings, overprint varnishes, printing inks and leather coatings. Furthermore, urethane (meth) acrylates are used in coating systems for flexible plastic substrates. In the electrical industry uretlian (meth) acrylates are used in screen printing inks and solder resists for printed circuit boards.
• (Meth) acrylated urethanes are formed in principle by reaction of an isocyanate group with a hydroxyl-containing acrylate or methacrylate monomer. When diisocyanates are used, the corresponding divinyl products are obtained.
• urethane (meth) acrylates are obtained by reacting a diisocyanate with a hydroxyl-containing acrylate or methacrylate monomer. If further hydroxyl-containing compounds, for example polyols, polyesters or polyethers having more than one hydroxyl group are used, a chain extension takes place.
• urethane (meth) acrylates can be prepared by the use of multiple hydroxylated starting materials.
• Flexible urethane (meth) acrylates arise z. B. by reaction of a diisocyanate with a long-chain diol and hydroxyl-containing monomer.
• a more or less hard urethane (meth) acrylate is formed by reacting a diisocyanate with a more or less highly branched multifunctional polyol and hydroxyl-containing monomer.
• a hydroxyl-containing precondensate or polymer can be reacted with a diisocyanate excess.
• the unsaturated urethane (meth) acrylate is then formed by hydroxyalkyl (meth) acrylate addition.
• the three main groups of urethane (meth) acrylates are the polyester urethane (meth) acrylates, the polyether urethane (meth) acrylates and the polyurethane (meth) acrylates.
• urethane (meth) acrylate compounds with very different properties. Modifications to the polymer backbone, for example with regard to chain length, concentration of reactive groups and other functional parameters, influence the property profile of the products in various respects.
• European Patent Application EP 1 306 399 describes a photocurable primer composition comprising an acrylic resin having on its side chain, bound by a urethane linker, a polymerizable unsaturated group, and a urethane (meth) acrylate oligomer containing at least one polymerizable unsaturated group per molecule contains.
• the primer composition is prepared by reacting a hydroxyl group-containing acrylic resin and a compound containing isocyanate groups and polymerizable unsaturated groups, or alternatively, reacting an isocyanate group-containing acrylic resin and a compound containing hydroxyl groups and polymerizable unsaturated groups.
• a further object of the present invention is to make available synthetic resins which are suitable for formulating free-radically curable mixtures of substances which are to be employed in the production of paints, and to provide these paints themselves.
• Composite plastic should therefore be based on (meth) acrylate, for example, composite materials and -Werk Published from phenolic, polyester or epoxy resin-based, inter alia, not UV-resistant, not colourfast and / or have no gloss and transparency. If necessary, the new system should provide high-quality, visually sophisticated surfaces, so that an overcoating device is not required.
• the applications can be diverse, so come as appropriate workpieces, for example, both pot handles, switches for electrical equipment, seats, wind turbine blades, decorative surfaces, gardening, benches or work surfaces and sinks in question.
• the invention should be characterized in that
• the curable composition which is used in the production of erfnidungsdorfen materials and workpieces should be characterized by an improved flow behavior and thus ultimately also by the fact that the fillers contained in it are better wetted.
• compositions can be provided. If desired, these compositions can be formulated in combination with additives to form free-radically curable compositions from which composite materials and workpieces as well as lacquers can be produced that meet the above-mentioned requirements.
• the composite materials and workpieces and coatings produced according to the invention are distinguished, in particular by a higher temperature and chemical resistance, from those known in the art and described above. Furthermore, the composite materials and -Werk publishede according to the invention, in contrast to those of the prior art, no cracks and voids, and a much lower shrinkage. There is also observed a higher color depth and a higher gloss of the composite materials and workpieces, as well as a thixotropic flow behavior of the respective curable compositions.
• Another special feature of the present invention is that a reduction of the curing time, as well as the energy supplied in comparison to the known prior art is possible.
• the synthetic resins according to the invention comprise a not insignificant proportion of relatively high molecular weight, multifunctional poly (meth) acrylates.
• the synthetic resins according to the invention comprise a not insignificant proportion of relatively high molecular weight, multifunctional poly (meth) acrylates.
• this increased proportion of relatively high molecular weight in particular, as will be shown below, partially crosslinked components, in the case of a final hardening, there are also less stresses which can otherwise have a negative effect on the quality of a workpiece produced in this way.
• Aliphatic structures in the poly (meth) acrylate urethane (meth) acrylates and the urethane (meth) acrylates provide the resin system with additional hydrophobicity and thus contribute to high chemical resistance.
• the UV resistance of the cured resin system according to the invention is also noteworthy.
• the components contained in the synthetic resins according to the invention are completely free of aromatic or other UV-resistant structures.
• the invention thus relates, in one embodiment, to a synthetic resin based on poly (meth) acrylate urethane (meth) acrylates in urethane (meth) acrylates obtainable by:
• urethane in the present invention means the addition product of the isocyanate group-reactive group (s) of the poly (meth) acrylate (III) and / or the (meth) acrylate (II) with the isocyanate groups of the isocyanate compound (IV Depending on the nature of the isocyanate-reactive radical (s), it is possible, for example, to form units which contain carbamic acid ester (-O- (CO) -NH-), carbonyloxy-carbamoyl- (- (CO) - 0- (CO) -NH-), carbamide (-NH- (CO) -NH-) and / or thiocarbamic acid-S- ester groups (-S- (CO) -NH-).
• the addition product (V) thus has a polymeric backbone (which is derived from (III)), which is linked via urethane units with at least one free isocyanate group-containing radicals (which are derived from (IV)).
• Addition product (V) can now be linked via its free isocyanate groups on the one hand in step (c) to form a partially crosslinked product with further poly (meth) acrylate (III) and on the other hand react in step (d) with further (meth) acrylate (II) ,
• step (d) reacts with (meth) acrylate (II) to form urethane (meth) acrylate.
• This assumes the function of a reactive diluent in the synthetic resin according to the invention.
• the isocyanate compound (IV) is suitably used in excess in step (c). By this is meant that there is an excess of molecules of the isocyanate compound (IV), based on the number of total isocyanate group-reactive radicals of the compound (III).
• the isocyanate compound (IV) is used in step (c) in an amount of 2.5 to 20 molar equivalent per mole of the isocyanate-reactive radicals.
• the percentage of the isocyanate groups of the isocyanate compound (IV) in step (c) which reacts with the reactive toward isocyanate groups can be, for example, set to a stoichiometric way, that is by the choice of an appropriate excess of the isocyanate compound (IV), based on the before the reaction of (III) with (IV) existing number of isocyanate-reactive radicals, said z. B. from the amount of monomers (I) and (II) used in step (a) can be calculated.
• the percentage of isocyanate groups of the isocyanate compound (IV) which react with the isocyanate group-reactive groups can be determined by determining the values according to the Reaction of step (c) remaining free isocyanate groups are found (eg by the titration method according to DIN 53185).
• the present invention relates to a synthetic resin in which the reaction in step (b) and / or the reaction in step (c) in the presence of a
• Solvent may according to the invention after and / or during the reaction according to step
• the isocyanate compound (IV) added in step (c) may temporarily take over its function.
• a reactive diluent can be added before and / or after step (d).
• step (a) the (meth) acrylate monomers (I) to the (meth) acrylate monomers (II) in a molar ratio of 100: 1 to 1: 1 are more preferred
• step (c) the
• Isocyanate compound (IV) in an amount of 2.5 to 20 molar equivalents, more preferably 4 to 12 molar equivalents, per mole of the isocyanate group-reactive groups.
• the (meth) acrylate monomers (II) in an amount of 1.0 to 1.1 molar equivalents per mole of the remaining isocyanate groups in the step (d).
• no free isocyanate groups should thus remain in the end product, the synthetic resin according to the invention.
• (meth) acrylates as used in the present invention includes both methacrylates and acrylates.
• one of the components used in step (a) is (meth) acrylate (I) which has no isocyanate-reactive radicals.
• (meth) acrylates (I) which have no isocyanate-reactive radicals preferably esters of (meth) acrylic acid use, wherein the alcohol portion of the ester preferably 1 to 18, more preferably 1 to 8, most preferably 1 to 4 , Carbon atoms and may be both straight-chain and branched.
• the alcohol portion of the ester may contain from 1 to 8 heteroatoms, such as oxygen, nitrogen or sulfur.
• esters of (meth) acrylic acid are more particularly: methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, n-butyl (meth) acrylate, i-butyl (meth) acrylate, n-hexyl (meth) acrylate, 2-ethylhexyl (meth) acrylate, isodecyl (meth) acrylate, dodecyl (meth) acrylate, phenoxyethyl (meth) acrylate, cyclohexyl (meth) acrylate, isobornyl (meth) acrylate, benzyl (meth) acrylate, ethylene glycol nonyl phenyl ether (meth) acrylate,
• methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, n-butyl (meth) acrylate and isobornyl (meth) acrylate are particularly preferably used.
• (meth) acrylate monomers (II) which have (one) isocyanate-reactive radical (s) are used in step (a).
• the (meth) acrylates according to the invention have radicals which are reactive toward isocyanate groups.
• suitable here are (meth) acrylate monomers which have at least one nucleophilic group which can undergo a chemical bond by reaction with isocyanate groups, such as.
• B is a group selected from a hydroxy, carboxy, amino and mercapto group, preferably a group selected from a hydroxyl, Amino and mercapto group, more preferably a group selected from a hydroxy and amino group, and most preferably a Hydröxy devis.
• the use of mixtures of (meth) acrylate monomers (II) carrying different of the aforementioned groups is also possible.
• the isocyanate group-reactive radicals (s) it is thus possible to form units which contain, for example, carbarnic acid ester groups, carbonyloxycarbarnoyl groups, carbamide groups and / or thiocarbamic acid S-ester groups.
• urethane units containing carbamic acid ester groups, carbamide groups and / or thiocarbamic acid S-ester groups, more preferably those containing carbamic acid ester groups and / or
• one or more, preferably one, two, three or four, more preferably one, of the nucleophilic groups used in the invention is attached to a C 2-10 hydrocarbon radical, preferably a C 2-4 Hydrocarbon radical, which in turn is bonded to the acid group of the (meth) acrylate by means of an ester or amide bond (such as in methylol (meth) acrylamide), preferably by means of an ester linkage
• the nucleophilic group is one or more particularly preferably one, two, three or four, on most preferably one, hydroxy group (s).
• the acrylic monomers are preferably used in practice with hydroxy functionality are hydroxy-C 2-1 O-alkyl acrylates, in particular hydroxy-C 2-1 O-alkyl acrylates such as hydroxyethyl acrylate (HEA) and hydroxypropyl acrylate (HPA).
• HOA hydroxyethyl acrylate
• HPA hydroxypropyl acrylate
• the corresponding less toxic hydroxy-C 2-1 o -acyl-methacrylates in particular hydroxy-C 2-10 -alkyl-methacrylates, such as 2-hydroxyethyl methacrylate and 2-hydroxypropyl methacrylate, are used.
• Other monoacrylates that can be used are for. B.
• diethylene glycol mono (meth) acrylate polyethylene glycol mono (meth) acrylate, polypropylene glycol nonionic (meth) acrylate and the equimolecular reaction product of glycidyl (meth) acrylate and (meth) acrylic acid.
• hydroxy-functional di (meth) acrylates such as trimethylol diacrylate (TMDA), trimethylolpropane di (meth) acrylate or glycerol di (meth) acrylate and hydroxy-functional triacrylates, such as pentaerythritol triacrylate (PETA).
• TMDA trimethylol diacrylate
• PETA pentaerythritol triacrylate
• Corresponding binders have particularly high crosslinking densities in coatings and / or composites.
• the use of (meth) acrylic acid and (meth) acrylamide as Monomers are less preferred in the present invention because they do not form very stable bonds with isocyanates.
• the reaction in step (b) and / or in step (c) can be carried out in the presence of a solvent.
• a solvent Preferably, in this case, the same solvent is used in both reactions.
• Suitable solvents are characterized by the fact that they do not nucleophilic groups such. B. hydroxy or carboxylic acid groups, and in that they have a suitable boiling point, preferably a boiling point of 40 to 15O 0 C, more preferably a boiling point of 80 to 13O 0 C, so that they are easily removed after completion and / or during the reaction can be.
• Preferred solvents which can be used according to the invention are esters such as. B. butyl acetate, ketones such.
• methyl ethyl ketone and methyl isobutyl ketone Etiler such.
• tetrahydrofuran and dibutyl ether and aromatic hydrocarbons such.
• toluene Suitable solvents are known in the art and can be readily selected by one skilled in the art depending on the reactants used.
• step (b) is preferably carried out by means of a free-radical solution polymerization of components (I) and (II). If a solvent is used in this reaction, the solvent can after the reaction. of step (b) or replaced with another solvent. In a preferred embodiment, the reaction mixture of step (b) is used directly in step (c) without replacement or removal of the solvent used.
• the free radical solution polymerization can be assisted by the use of a catalyst.
• Preferred catalysts are radical chain initiators.
• suitable radical chain initiators known in the art include diacyl peroxides such as benzoyl peroxide or dilauryl peroxide, alkyl hydroperoxides such as t-butyl hydroperoxide or cumene hydroperoxide, alkyl peresters such as t-butyl perbenzoate and t-butyl peroxy-2-ethylhexanoate, and azo compounds such as azodiisobutyronitrile.
• the catalyst for.
• radical initiator is preferably used in an amount of 1 to 20 wt .-%, preferably 2 to 15 wt .-%, based on the total amount of components (I) and (II).
• a polymerization regulator z As mercaptans such as 1-dodecanethiol or alcohols such as 2-propanol are used, preferably in each case in an amount of 0 to 3 wt .-%, based on the total amount of components (I) and (II).
• To control the molecular size is also a reaction under elevated pressure, preferably a pressure of more than atmospheric pressure (which is usually given as 1.01325 bar) to 8 bar, more preferably from 1.5 to 8 bar, and most preferably from 1, 5 to 5 bar, possible.
• elevated pressure preferably a pressure of more than atmospheric pressure (which is usually given as 1.01325 bar) to 8 bar, more preferably from 1.5 to 8 bar, and most preferably from 1, 5 to 5 bar, possible.
• elevated temperatures up to about 250 ° C (see below).
• step (b) gives poly (meth) acrylates (III) which have radicals reactive with isocyanate groups.
• the formation of the poly (meth) acrylates (III) according to the invention is usually carried out using suitable catalysts, for. Radical radical initiator, by reacting the above (meth) acrylates (II) having (an) isocyanate group-reactive radical (s) with the above (meth) acrylates (I) having no isocyanate-reactive radicals , This is preferably done in a suitable solvent.
• Preferred amounts of solvent are 10 to 150 wt .-%, in particular 50 to 100 wt .-%, based on components (I) and (II).
• the reaction is conveniently carried out at temperatures in the range of the boiling point of the solvent, so under photosfmss. Preferred temperatures are at 40 to 150 0 C, in particular at 80 to 130 0 C. Under pressure can be used advantageously at temperatures of 40 to 250 0 C, in particular from 100 to 180 °.
• the poly (meth) acrylates (III) preferably have 1 to 100, more preferably 1 to 10, isocyanate-reactive radicals, and are preferably from ten to a thousand (meth) acrylate Monomerbaustemen type I and II, preferably in a ratio of 100: 1 to 1: 1, more preferably in a ratio of 20: 1 to 4: 1, together.
• Preferred poly (meth) acrylates (III) have a weight average molecular weight (M w ) of about 2,000 to 10,000 g / mol, preferably about 4,000 to 8,000 g / mol, most preferably about 6,000 g / mol (at a molecular weight distribution of about 400 to about 30,000 g / mol).
• the poly (meth) acrylate (III) from step (b) is reacted in step (c) with an isocyanate compound (IV) having more than one isocyanate group (polyisocyanate) in an addition reaction.
• step (c) a plurality of different poly (meth) acrylates (III) can also be used in step (c).
• aliphatic, aromatic and heterocyclic isocyanates containing two or more isocyanate groups in one molecule are used as polyisocyanates according to the invention.
• polyisocyanates (IV) examples are:
• Diisocyanatodiphenyl ether 4,6-dimethyl-1,3-phenyl diisocyanate, 9,10-anthracenediisocyanate, 2,4,6-toluene triisocyanate, 2,4,4'-triisocyanatodiphenyl ether, 1,4-tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate (HDI ), 1,10-decamethylene diisocyanate, 1,3-
• oligomers of monomeric isocyanuric compounds as defined above, preferably those of the abovementioned examples of monomeric isocyanuric compounds
• the oligomers suitable for use in the present invention have two or more isocyanate groups
• trimers of isocyanates as defined above such as the trimer of hexamethylene triisocyanate (HDI), which has a molecular weight of 504.6 g / mol. and the trimer of isophorone diisocyanate (IPDI), which has a molecular weight of 666.9 g / mol. Both are trifunctional with respect to the isocyanate group.
• reaction products of monomeric isocyanate compounds as defined above preferably those of the above-listed examples of monomeric isocyanate compounds
• the reaction products suitable for use in the present invention have two or more isocyanate groups.
• Examples of such reaction products are compounds obtained by reaction of the monomeric isocyanate compounds as defined above with polyols, such as. As ethyl glycol, propyl glycol, neopentyl glycol, hexanediol, trimethylolpropane, glycerol and hexane triol, or be obtained with water.
• Examples include polyisocyanate-polyol adducts such as the adduct of a molecule of trimethylolpropane with three molecules of toluene diisocyanate (TDI), which is trifunctional with respect to the isocyanate group, and biuretics such as the reaction product of three molecules of hexamethylene triisocyanate (HDI) with one molecule of water with CO 2 elimination, which is bifunctional with respect to the isocyanate group.
• TDI toluene diisocyanate
• biuretics such as the reaction product of three molecules of hexamethylene triisocyanate (HDI) with one molecule of water with CO 2 elimination, which is bifunctional with respect to the isocyanate group.
• aliphatic diisocyanates such as HDI or IDPI produces particularly light-stable and discoloration-resistant synthetic resins.
• Preferred reaction products of the reaction of poly (meth) acrylate (III) with isocyanate (IV) usually have a molecular weight distribution of about 1,000 to about 200,000 g / mol.
• the high molecular weight speaks, in comparison with the molecular weight before a reaction with the isocyanate compound (FV), for a partial crosslinking of the poly (meth) acrylate urethane (meth) acrylates according to the invention.
• Such can be done, for example, when a portion of the molecules of the isocyanate compound (IV) having more than one isocyanate group reacts with the isocyanate-reactive groups of more than one poly (meth) acrylate chain (III). In this way, there is an increase of the weight average by a factor of 2 to 20, that is to say a crosslinking of on average about 2 to 20 molecules of the poly (meth) acrylate (III).
• step (c) the solvent used may be removed.
• the reaction mixture from step (c) is reacted with (meth) acrylate monomers (II) in step (d), the isocyanate-reactive radicals of the (meth) acrylate monomers (II) adding as part of an addition reaction to the remaining isocyanate groups.
• step (c) and / or (d) can be supported according to the invention by the use of suitable catalysts.
• catalysts optionally find the usual urethanization catalysts such. As triethylamine, DABCO or dibutyltin dilaurate use.
• the adjustment to a suitable viscosity can be carried out before or after step (d) by adding (meth) acrylates and / or suitable reactive diluents.
• reactive diluents known in the art low molecular weight compounds can be used which preferably have 1 to 5 reactive double bonds.
• monofunctional reactive thinner a reactive double bond
• difunctional reactive diluents (2 reactive double bonds), such as hexanediol diacrylate or tripropylene glycol diacrylate, and tri to hexafunctional reactive diluents (3 to 6 reactive double bonds) which cause an increase in the crosslinking density, such as trimethylolpropane tri (meth) acrylate, ethoxylated or propoxylated trimethylolpropane triacrylate, propoxylated Glycerol triacrylate, pentaerythritol triacrylate, pentaerythritol tetraacrylate, ditrimethylolpropane tetraacrylate or dipentaerythritol hexaacrylate.
• monofunctional reactive thinner such as isobornyl acrylate or N-vinylpyrrolidon
• the reactive diluents have two important functions. On the one hand, they reduce the viscosity of the free-radically curable composition, on the other hand, they strongly influence the physical and chemical properties of the respective resulting composite material or paint.
• a typical composition may contain, for example, 52% by weight of polymer, 25% by weight of urethane (meth) acrylate and 23% by weight of methyl (meth) acrylate and / or reactive diluent.
• the proportion of urethane groups in these, the ratio of these components and ultimately, of course, depending on the temperature, the material liquid or waxy pasty is present.
• the fact that the material can be waxy pasty even at room temperature, depending on the circumstances listed above, is not insignificantly due to the urethane groups contained, they are characterized by their high polarity and ability to hydrogen bond.
• step (c) mixtures of one or more poly (meth) acrylates (III) with other polyols such.
• B trimethylolpropane, di (trimethylolpropane), pentaerythritol, di (pentaerythritol), neopentyl glycol and methylpropanediol and polyester polyols, polycarbonate diols or polyether polyols such.
• neopentyl glycol propoxylate, trimethylolpropane ethoxylate, trimethylolpropane propoxylate, pentaerythritol ethoxylate and pentaerythritol propoxylate can be used.
• the synthetic resin of the invention produced in step (d) is used either alone or in combination with additives as a radically curable composition.
• the radically curable compositions according to the invention are preferably prepared by mixing at least one synthetic resin described above based on poly (meth) acrylate urethane (meth) acrylates in urethane (meth) acrylates and optionally (meth) acrylates and / or reactive diluents optionally with one or more additives as known to those skilled in the art, preferably selected from pigments (pigment pastes) such as.
• White pigments such as titanium oxide, black pigments such as carbon blacks and iron oxide black, blue pigments such as copper phthalocyanines, green pigments such as chromium oxide green, yellow pigments such as iron oxide yellow, red pigments such as iron oxide red and other color pigments; Dyes such. Aza [18] annulenes, nitro dyes, nitrosoverses, azo dyes, carbonyl dyes and sulfur dyes; Fillers such. B.
• alkaline earth sulfates such as barite or Blancfixe, Telgnesiumsilikaten such as talc, Alun ⁇ iniumsilikaten such as mica, organic and inorganic fibers such as glass fibers, Microkohlgehügehi from süikat ⁇ schem material, aluminum hydroxide, alumina, chalk, iron mica and graphite, which are optionally coated with epoxy resin, polyurethane resin or water glass; and excipients such.
• Fumed silica bentonites (as anti-settling agents), stearic acid or waxes (as internal release agents), wetting agents and defoamers; and multifunctional crosslinkers such.
• Preferred amounts of additives are from 30 to 90% by weight, preferably from 40 to 70% by weight, based on the total composition.
• the radically curable compositions according to the invention preferably contain catalysts which promote radical polymerization, in particular radical chain initiators, more preferably peroxides. These can be activated, for example, thermally or by the action of light. Examples of suitable radical chain initiators, including those for particularly suitable peroxides, are listed above.
• Stabilizers or inhibitors suitable for preventing premature polymerization are listed below by way of example: 1,4-dihydrobenzene (hydroquinone, HQ), 4-methoxihydroxybenzene (hydroquinone monomethyl ether, HQME or MEHQ), 2,6-di-t-butylhydroquinone (DTBHQ) , Phenothiazine (thiodiphenylamine, PTZ), nitrobenzene.
• Nitrobenzene is optionally added to suppress the likewise undesirable gas phase polymerization in the preparation.
• the presence of oxygen is advantageous in the production, but carries the risk of ignitable mixtures.
• compositions described above composite materials and -Werk publishede can be prepared according to the invention.
• a radically curable composition according to the invention is placed in a mold.
• the compositions of the invention which are characterized by a very good flow behavior - due to the good wetting of the aggregates - this can be done faster than with comparable mixtures, for example those based on MMA / PMMA.
• the mass in the form z. B. heated with hot steam over preferably 20 to 30 minutes at a pressure of preferably 3 to 4 bar to preferably 70 to 13O 0 C.
• the composite material or the corresponding workpiece can be removed from the mold and further processed in a known manner.
• Workpieces such. As pot handles, switches for electrical equipment, seats, wind turbine blades, decorative surfaces, garden plates, benches, work surfaces and sinks can be prepared according to the invention under pressure, heat and shaping of the above-described radically curable compositions by free radical polymerization.
• the present invention comprises a process for producing workpieces of composite materials obtainable by curing radically curable compositions according to the invention containing synthetic resins according to the invention, the process comprising, in addition to steps (a) to (d) above Steps includes:
• step (e) providing a composition which has at least one mixture of the type obtained in step (d), optionally diluted to a desired viscosity by addition of (meth) acrylates and / or suitable reactive diluents, and optionally one or more additives, such as are known in the art, selected from z.
• additives such as are known in the art, selected from z.
• pigments, dyes, fillers, excipients, peroxides as catalysts and multifunctional crosslinkers (suitable individual examples of the respective types of additives are listed above) contains;
• the composite materials or -Werk publishede invention are characterized by a high hardness and impact resistance, gloss, color depth, clarity, shape fastness, hydrophobicity, oleophobicity, scratch resistance and high resistance to chemicals, temperature and UV light, as well as in that they free of microcracks and bubbles.
• the synthetic resins according to the invention can also be used, for example as part of a free-radically curable composition, for the production of paints.
• the desired viscosity of the composition can optionally be adjusted with at least one (meth) acrylate and / or reactive diluent, preferably with a reactive diluent. Examples of suitable reactive diluents are listed above. In this way, the use of conventional solvents and other volatile components which can be included in the paint when cured, can be substantially avoided. The resulting benefits have already been explained.
• a free-radically curable composition according to the invention is subjected to curing, preferably by exposure to UV light.
• a provided for curing by the action of UV light composition additionally contains a photoinitiator, such as. Example, a activatable by exposure to light, the free-radical polymerization supporting catalyst, in particular a thus activatable radical chain starter.
• the paint of the invention comprises the composition in cured form.
• the poly (meth) acrylate urethane (meth) acrylates according to the invention are distinguished, in particular, by the associated preparation method, which in a preferred embodiment stripping the solution of the reaction product of poly (meth) acrylate (III). with an isocyanate compound (IV), in the presence of the isocyanate compound and thus ultimately allows access to the synthetic resins according to the invention, which despite high molecular weight, preferably having a molecular weight of 1,000 to 200,000 g / mol, of the contained poly (meth) acrylate urethane - (meth) acrylates - if necessary - contain only reactive solvents.
• Example A Preparation of a synthetic resin based on poly (meth) acrylate urethane (meth) acrylates in urethane (meth) acrylates
• hexamethylene diisocyanate (HDI)
• HDI hexamethylene diisocyanate
• the mixture is then distilled off under nitrogen until a temperature of 180 ° C is reached. If only a small amount of butyl acetate is added, the nitrogen supply is stopped and the residue of butyl acetate is removed under reduced pressure. After completion of the distillation, the vacuum is broken with nitrogen and then cooled to 12O 0 C, added 2.90 kg of isophorone diisocyanate (IPDI) to reduce the viscosity, then further cooled to 8O 0 C and upon reaching 8O 0 C 0.04 kg of hydroquinone monomethyl ether in 16.11 kg of methyl methacrylate for stabilization and dilution.
• IPDI isophorone diisocyanate
• a solution of a poly (meth) acrylate urethane (meth) acrylate is obtained which is composed as follows: about 52% by weight poly (meth) acrylate urethane (meth) acrylate, about 25% by weight % monomeric methyl methacrylate (MMA), about 23 wt .-% urethane (meth) acrylate.
• the loading of a mold for a workpiece is carried out with the free-radically curable composition B within 70 seconds.
• this composite material has good mechanical properties, as well as high chemical and temperature resistance.
• z. B. in the hot-cold water alternating test (15 ° C / 90 ° C) after 500 cycles no cracks or whitening of the hue.
• the composition used in the production of these optimized materials and workpieces is characterized by improved flow behavior and thus ultimately by the fact that the fillers contained in it are better wetted.
• the materials according to the invention thus meet the requirements placed on them in comparison with the known materials, such as no or fewer and smaller voids and cracks, a higher resistance to chemicals and temperatures, no (n) or less shrinkage and emissions in their manufacture, manufacturability in less time and one better look; while retaining the positive properties such as impact strength, UV resistance and hydro- and oleophobia.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• General Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Wood Science & Technology (AREA)
• Macromonomer-Based Addition Polymer (AREA)
• Polyurethanes Or Polyureas (AREA)
• Paints Or Removers (AREA)

Priority Applications (6)

Applications Claiming Priority (2)

Publications (1)

Family

ID=36097134

Family Applications (1)

Country Status (9)

Families Citing this family (10)

Citations (3)

Family Cites Families (2)

• 2005
  • 2005-02-01 DE DE102005004639A patent/DE102005004639A1/de not_active Ceased
• 2006
  • 2006-01-11 JP JP2007553488A patent/JP2008528771A/ja active Pending
  • 2006-01-11 EP EP06700673A patent/EP1846461B1/de not_active Not-in-force
  • 2006-01-11 AT AT06700673T patent/ATE404592T1/de active
  • 2006-01-11 WO PCT/EP2006/000188 patent/WO2006081916A1/de not_active Ceased
  • 2006-01-11 CA CA002596464A patent/CA2596464A1/en not_active Abandoned
  • 2006-01-11 ES ES06700673T patent/ES2312105T3/es active Active
  • 2006-01-11 PL PL06700673T patent/PL1846461T3/pl unknown
  • 2006-01-11 DE DE502006001329T patent/DE502006001329D1/de active Active
  • 2006-01-11 US US11/883,403 patent/US20100093924A1/en not_active Abandoned

Patent Citations (3)

Also Published As

Similar Documents

Legal Events