DE10207401A1 - Highly-filled silicon-organic paste containing nano- and-or micro-hybrid capsules for abrasion-resistant coatings, made by reacting nano- and micro-scale oxide particles with organo-functional silane in a curable resin - Google Patents

Abstract

Highly-filled, paste-like silicon-organic compositions containing nano- and/or micro-hybrid capsules for scratch- and abrasion-resistant coatings, obtained by reacting nano- and/or micro-scale oxide particles in a kneader or disperser with a curable resin, an organo-functional silane and optionally a silicate ester and/or organosiloxane. Highly-filled, paste-like, organosilicon compositions (I) containing nano- and/or micro-hybrid capsules for scratch- and/or abrasion-resistant coatings. The capsules consist of an oxide core (A) containing nano- or micro-scale oxide particles (KA-O) of components (a) and/or (b) and a silicon-organic shell (B) containing component(s) of formula (Si'O-)xSi-R (Ia) which may be attached to core (A) via covalent bonds of formula (KA-O)-((Si'O-)xSiR) (Ib) in which the free valencies of Si are attached to (KA-O)-, SiO- and/or -Z and the free valencies of Si' are attached to (KA-O)-, SiO-, -R and/or -Z, with not more than one group R on each Si or Si'; R = an organo-functional group; x = 0-20; Z = hydroxyl or alkoxy. These compositions are obtained by reacting (i) oxide particles selected from (a) nano- or micro-scale oxides and/or mixed oxides of metals or metalloids of Main Groups 2-6, Sub-Groups 1-8 or lanthanides, (b) micro-scale corundum and (c) a mixture of (a) and (b), with (ii) organo-functional silane(s) of formula R<1>sR<2>rSiY4-s-r (II) in which R<1>, R<2> = 1-50C alkyl, 2-6C alkenyl, chloroalkyl, isocyanoalkyl, cyanoalkyl, fluoroalkyl, aryl, acylalkyl, (meth)acryloxyalkyl, polysulfanalkyl, mercaptoalkyl, thiacyamidalkyl, glycidyloxyalkyl, aminoalkyl, diaminoalkyl, triaminoalkyl, carbonatoalkyl or ureidoalkyl; Y = methoxy, ethoxy, n- or iso-propoxy, or 2-methoxyethoxy; s = 1, 2 or 3; r = 0, 1 or 2; (s+r) = not more than 3, (iii) optionally a monomeric and/or oligomeric silicate ester with methoxy, ethoxy, n-propoxy or iso-propoxy groups and an average degree of oligomerisation of 1-50 and (iv) optionally an organofunctional siloxane in which each silicon atom is attached to an alkyl, fluoroalkyl, cyanoalkyl, isocyanoalkyl, alkenyl, mono-, di- or tri-aminoalkyl, alkoxyalkyl, hydroxyalkyl, acylalkyl, glycidyloxyalkyl, (meth)acryloxyalkyl, mercaptoalkyl, ureidoalkyl, aryl or alkoxy group and the free silicon valencies are attached to methoxy, ethoxy or hydroxy groups. The reaction is carried out in situ in a liquid, curable synthetic resin or resin precursor, using 10-300 parts by weight (pts. wt.) oxide particles (i) to 100 pts. wt. resin, and working in a kneader or a dispersion apparatus. An Independent claim is also included for a method as described above for the production of (I).

Description

The present invention relates to an organosilicon nano and / or Micro-hybrid capsule-containing composition for scratch and abrasion resistant Coatings, wherein the organosilicon nano or micro hybrid system small metal oxide cores A and an essentially complete, organosilicon coating B and the composition by a Implementation of metal oxide particles (KA-O) and at least one organofunctional silicon compound, the one organofunctional group and at least one hydrolyzable group or has at least one hydroxyl group, in a synthetic resin or in one Resin precursor compound is available. Furthermore, the present concerns Invention the use of such compositions as a basis for paints Creation of a scratch-resistant and abrasion-resistant coating on a substrate as well as correspondingly scratch and abrasion resistant coated articles.

It is known the surface properties of sol or gel particles or of Metal or semimetal oxides by treatment with a hydrolyzable Modify organosilane or organosiloxane, usually one only single-layer silane layer binds to the oxide or sol gel particles. So treated Oxides or sol or gel particles, for example inorganic pigments or Fillers can be introduced into a polymer matrix, especially in films as well as in coating compositions and coatings that can be produced with them. Usually is however, the scratch and abrasion resistance of such polymer systems is low.

DE 198 46 660 discloses nanoscale, surface-modified oxide or Mixed oxide particles that are covalently bound to the oxide particle organosilicon groups are encased, the organofunctional groups are described as reactive groups and are usually oriented towards the outside are so that they polymerize with the polymer material when the Prepolymer can be integrated into the polymer matrix. The manufacturing process such coating agent is expensive because the organosilane and the oxidic  Components are alternately incorporated into the prepolymer.

DE 198 46 659 has the same seniority as DE 198 46 660 and relates to one Layer material, which is provided with a scratch-resistant synthetic resin layer, which also contains nanoscale, surface-modified oxide particles. DE 198 46 659 specifically teaches the use of acryloxyalkylsilanes to create an envelope nanoscale oxide particles which have reactive, radiation-crosslinkable groups. The coating agent is also produced here by a time-consuming implementation of a nanoscale silica with 3-meth acryloxypropyltrimethoxysilane (DYNASYLAN® MEMO) in an acrylate formulation in the presence of water, an acid and a wetting agent. Again have to the components are brought together alternately in a special order become.

In addition, hydrolyzable silane components are ethylenic unsaturated organo groups mostly high-priced feedstocks. Further tends DYNASYLAN® MEMO already in the presence of small traces Polymerization initiating substance or radiation to react, thereby the viscosity of a corresponding preparation can increase drastically. to To avoid undesirable polymerization, stabilizers must be added become. Therefore, it is often difficult to handle the input materials and the To master the manufacture of such coating systems.

Furthermore, said coating compositions are often highly viscous and mostly contain only a small proportion of oxide particles, which affects the scratch resistance of the later coating affects. It is also difficult to find such highly viscous Apply coating agent to a substrate, especially when it is thin, tearable substrates. The scratch resistance is often more available Coatings in need of improvement. With such highly viscous systems in addition, a special complex application device is required. Frequently If such highly viscous coating agents are also added solvents, those to increase organic emissions (VOC problem, VOC = "volatile  organic compounds ").

2 mg of abrasion were removed on a commercially available abrasion-resistant PU lacquer 50 revolutions measured (Taber Abraser test according to DIN 68 861).

According to the teaching of the not yet published German patent applications 101 00 631 and 101 00 633 can be essentially scratch-resistant (DIN 53 799) Coatings are generated. Unfortunately, such coating systems can be used for Applications where not only scratch resistance but also adequate Abrasion resistance (Haze according to DIN 52 347 / ASTM D-1044 and abrasion according to DIN 68 861) is not required, for example for wood painting, Plastic and parquet floors. They can also use higher-filled systems Show inhomogeneities, which affects the surface quality of the later Coating has an adverse effect. Furthermore, at this point the German Patent application 101 41 690 with the title "Organosilicon nano- / Micro hybrid systems containing composition for scratch and abrasion resistant Coatings "pointed out.

Since users often use such organosilicon nano or micro hybrid systems containing compositions for making or modifying them Use paint formulations for scratch and abrasion resistant equipment wanted to provide a system that was as homogeneous as possible and can be used as variably as possible, in particular with regard to the solids content, where appropriate paint formulations for producing scratch and / or wear-resistant coatings can use.

According to the invention, the object is achieved in accordance with the specifications of Claims resolved.

It was found that by carrying out the so-called in-situ reaction as they did in particular from DE 101 00 631, DE 101 00 633 and DE 101 41 690 is removed, on a three-roll mill, in a cone mixer, in a kneader  or in a dispersant with a good dispersing effect, - as described for example under the name Torusmill® is offered by VMA-Getzmann GmbH (EP 0 850 106 B1), wherein in the case of the present invention, when used the Torusmill® only uses the dissolver or the dissolver disc and uses, d. H. that the Torusmill® immersion mill is not used here and the immersion mill function is not used in the present manufacturing process -, pastes that are stable in storage and largely aging, d. H. highly filled, in excellent way homogeneous organosilicon nano and / or Compositions containing micro-hybrid capsules by incorporation at least one organosilicon compound and microscale corundum and / or nanoscale oxide in a synthetic resin or Resin precursor compound are available.

By diluting such a concentrate or paste with a Prepolymer, for example an acrylate, preferably 1 part by weight of paste with 1 to 5 parts by weight, particularly preferably 1 to 3 parts by weight, in particular 1.5 parts by weight Parts of acrylate, one can get paint systems after radiation curing excellent scratch and abrasion resistant coatings result.

Pastes can also be used in existing resin-based coating systems incorporate in a simple manner and advantageous for producing scratch and abrasion resistant Use coatings.

Pastes can also be obtained in a particularly simple and economical manner Way with z. B. acrylic thinners such as DPGDA or HDDA, and optionally add other known paint additives and become one ready-to-use peroxidically or radiation-crosslinkable scratch and / or Dilute abrasion-resistant paint in the desired way.

Suitably, the diluent or a lacquer is placed in front of it the paste according to the invention is stirred in in a simple and economical manner. The present pastes are therefore characterized by a surprisingly advantageous one  Processability both in the production of the pastes and in application after dilution.

In addition, practice shows that even with a high proportion of corundum in the Composition no above average wear on the mix and Application devices can be determined, which also applies to the organosilicon Coating of the oxide particles can be returned.

It was also found that pastes according to the invention after dilution with a suitable diluent or by incorporation into organic Varnish systems by the user in an advantageous manner for generation in particular scratch and abrasion resistant coatings on substrates as well as corresponding articles can be used from it.

Under a curable resin or a precursor to a curable Synthetic resin, d. H. a liquid prepolymer or a mixture thereof Prepolymers, here and below, for example, acrylates, methacrylates, Epoxy, polyurethane, unsaturated polyester or mixtures thereof understood.

Furthermore, one essentially obtains according to the present procedure completely and multilayered silicon-organic coated oxide particles, d. H. Cores A, which are directly dispersed in an advantageous manner in a hardenable synthetic resin or a precursor of a curable synthetic resin.

In addition, this is obtained according to the present procedure organosilicon nano or micro hybrid system in the prepolymer especially incorporated homogeneously.

Compositions thus obtained are characterized by a surprising advantageous processability in manufacture and application, since practice shows that despite the proportion of corundum in the composition by the organosilicon  Coating the corundum particles no additional wear on the mixing and Application devices can be determined.

A dilatant behavior of paints can generally and in technical processes pose a problem especially for coatings with special coatings. in the In general, one strives for such a dilatant coating system Viscosity up to 2,500 mPa.s. Solvents according to the invention preferably have free coating agents have a viscosity of <500 to 2000 mPa.s, especially preferably from 800 to 1000 mPa.s. For a roller application, the Viscosity are in the range 0.8 to 1.2 Pa.s.

It has also been found that in addition to one that is usually applicable Dilution of the paste or viscous lacquers and a temperature regime during the Coating (typically approx. 60 ° C) special paint additives the viscosity of the Can effectively reduce dispersions. With the addition of z. B. 9% by mass of one Wording such as B. DPGDA with 30% by mass Aerosil OX 50 and 9% by mass DYNASYLAN VTMO, one can see the rheological behavior of a highly dilatant Further improve dispersion or a varnish.

Coating systems with DYNASYLAN® PTMO as a silane component can dilate Show behavior. By using mixtures of DYNASYLAN® PTMO under Addition of VTMO or a corresponding oligomeric propyl and / or One can use a vinyl functional alkoxysiloxane or mixtures thereof achieve favorable rheological behavior.

Thus, for example, a mixture of is preferred in the present process PTMO and VTMO or propyl-functional alkoxysiloxanes or vinyl-functional Alkoxysiloxanes or propyl / vinyl functional alkoxysiloxanes - by just a few To name examples - or mixtures thereof as organosilicon components.

The use of oligomeric organoalkoxysilanes, such as specifically produced condensates or cocondensates, for example starting from at least one n-  Propyltrialkoxysilane, perfluoro-1,1,2,2-tetrahydroalkyltrialkoxysilane, phenyltrialkoxy silane, 3-methacryloxypropyltrialkoxysilane and / or vinyltrialkoxysilane, each of which Corresponding organofunctional alkoxysiloxanes are also special Advantage, since said siloxanes practically not compared to monomeric silanes are volatile and therefore do not evaporate under processing conditions and preferably no educt losses are recorded in the present process. Ethoxy and methoxy are preferred as alkoxy groups.

The said coating is suitably cured photochemically UV radiation or by irradiation with electron beams. Usually leads irradiation at a temperature of 10 to 60 ° C, advantageously at Ambient temperature, by.

So you can according to the invention in a simple and economical manner Pastes containing organosilicon nano / micro hybrid capsules Manufacture coating agents with which one is excellent scratch and abrasion resistant Can produce coatings.

The present invention therefore relates to an essentially particularly homogeneous, highly filled, pasty composition comprising organosilicon nano- and / or micro-hybrid capsules (also called paste for short) for scratch and / or abrasion-resistant coatings,
wherein an organosilicon nano or micro hybrid capsule consists of an oxidic core A, which contains at least one nanoscale or microscale oxide particle (KA-O) of components (a) and / or (b), and an organosilicon coating B and the organosilicon coating B at least one organosilicon component of the general formula Ia

(Si'O-) _x Si-R (Ia),

where R is an organofunctional group, as is also apparent from formula II in the form of R ¹ and R ² , and x is a number from 0 to 20, the free valences of Si by SiO- and / or -Z and the free Valences of Si 'are saturated by SiO-, -R and / or -Z, the groups Z are identical or different and represent hydroxyl or alkoxy radicals, and each Si or Si' of the coating B bears a maximum of one group R,
contains and / or the organosilicon component of the coating B via one or more covalent bonds of the general formula Ib

(KA-O) - [(Si'O-) _x Si-R] (Ib),

where R has the meaning given above and x is a number from 0 to 20, the free valences of Si by (KA-O) -, SiO- and / or -Z and the free valences of Si 'by (KA-O ) -, SiO-, -R and / or -Z are saturated, the groups Z are the same or different and represent hydroxyl or alkoxy radicals, and each Si or Si 'of the coating B carries at most one group R,
is bound to the core A (KA-O),
available through an implementation of

• a) Oxide particles from the series
  • a) at least one nanoscale oxide and / or mixed oxide of at least one metal or semimetal of the second to sixth main group, the first to eighth subgroup of the periodic table of the elements or the lanthanides or
  • b) a microscale corundum or
  • c) an oxide particle mixture of (a) and (b),
  With
• b) at least one organofunctional silane of the general formula II
  R ¹ _s R ² _r SiY _(4-sr) (II),
  wherein the groups R ¹ and R ^{2 are the} same or different and each have a linear, branched or cyclic alkyl group with 1 to 50 C atoms, preferably with 1 to 16 C atoms, an alkenyl group with 2 to 6 C atoms, a chloroalkyl -, isocyanoalkyl, cyanoalkyl, fluoroalkyl, aryl, acylalkyl, acryloxyalkyl, methacryloxyalkyl, polysulfanalkyl, mercaptoalkyl, thiacyamidalkyl, glycidyloxyalkyl, aminoalkyl, diaminoalkyl, triaminoalkyl, carbonatoalkyl or a ureidoalkyl Represent a group, Y represents a methoxy, ethoxy, i-propoxy, n-propoxy or 2-methoxyethoxy group and s is 1 or 2 or 3 and r is 0 or 1 or 2, with the proviso (s + r) ≦ 3,
  and
• c) optionally a monomeric and / or oligomeric silicic acid ester which carries methoxy, ethoxy, n-propoxy or i-propoxy groups and has an average degree of oligomerization of 1 to 50, for example tetramethoxysilane, such as DYNASIL® M, tetraethoxysilane, such as DYNASIL® A, tetrapropoxysilane, such as DYNASIL® P, or an oligomeric ethyl silicate, such as DYNASIL® 40,
  and
• d) optionally an organofunctional siloxane, the functionalities of which are the same or different and each Si atom in the siloxane is a functionality from the series alkyl, fluoroalkyl, cyanoalkyl, isocyanoalkyl, alkenyl, aminoalkyl, diaminoalkyl, triaminoalkyl, alkoxyalkyl, hydroxyalkyl, acylalkyl, glycidyloxyalkyl, acryloxyalkyl , Methacryloxyalkyl, mercaptoalkyl, ureidoalkyl, aryl or alkoxy and the remaining free valences of the Si atoms in the siloxane are saturated by methoxy or ethoxy or hydroxyl groups; preference is given to those siloxanes with an average degree of oligomerization of 1 to 20, preferably with an average degree of oligomerization of 2 to 10, as can be seen in particular from German patent applications 199 55 047, 199 61 972, 100 56 343, 101 51 264, 102 02 389, EP 0 518 057, EP 0 590 270, EP 0 716 127, EP 0 716 128, EP 0 760 372, EP 0 814 110, EP 0 832 911, EP 0 846 717, EP 0 846 716, EP 0 846 715, EP 0 953 591, EP 0 955 344, EP 0 960 921, EP 0 978 525, EP 0 930 342, EP 0 997 469, EP 1 031 593 and EP 0 075 697,
  wherein the reaction takes place in situ in a liquid, curable synthetic resin or a precursor stage of a synthetic resin, the content of oxide particles of component (i) is 10 to 300 parts by weight, based on 100 parts by weight of the synthetic resin component used, and the Implemented in a kneading or dispersing unit with an appropriate dispersing effect.

Kneading units are such in the present invention To understand processing units that in addition to the usual mixing effect Kneading action and optionally additional dispersing action, d. H. effects which contribute to the homogenization of the highly filled synthetic resin mass. Suitably, one can be used to prepare the paste according to the invention Roller mill, cone mixer, extruder with mixing and kneading function, kneader or one Use a powerful dispersing unit.

The alkoxy radicals of groups Z are those with a linear, cyclic or branched alkyl radical having 1 to 18 carbon atoms are preferred, in particular methoxy, Ethoxy, i- or n-propoxy groups are preferred.

In organosilicon nano or micro hybrid capsules according to the invention the weight ratio between core A and sheath B preferably 0.5: 1 to 100: 1, particularly preferably 1: 1 to 2: 1 inventive method a feed ratio of the oxidic Component (i), the organosilicon components (ii) to (iv) and the Resin components from 0.2: 0.5: 1 to 3: 1: 1 parts by weight, especially from 1: 1: 1 to 2: 1: 1 parts by weight. The weight ratio of the organosilicon components (ii), (iii) and (iv) with each other from 1: 0: 0 via 1: 1: 0 and 1: 0: 1 and 0: 1: 1 to 0: 0: 1 are sufficient.  

Suitably, a core A of the organosilicon organic / micro hybrid capsules according to the invention consists of at least one nanoscale oxide and / or mixed oxide, oxide hydroxides are hereby included, from the series of the elements Si, Al, Ti and / or Zr, for example SiO ₂ , such as pyrogenically prepared silica , Silicates, aluminum oxide, aluminum hydroxide, aluminosilicates, TiO ₂ , titanates, ZrO ₂ or zirconates or from a microscale corundum particle.

According to the invention, component (a) of the oxide particle mixture is used here (i) preferably at least one nanoscale oxide and / or mixed oxide from the Series of the elements Si, Al, Ti and / or Zr, the nanoscale oxide preferably has an average grain size of 1 to 200 nm. Particularly preferred as component (a) a nanoscale silica is used.

A further preferred component (b) of the oxide particle mixture (i) is a microscale corundum (α-Al ₂ O ₃ ), this preferably having an average grain size of 3 to 40 μm, particularly preferably 9 to 18 μm, very particularly preferably 12 to 15 µm.

The present invention furthermore relates to a process for the preparation of a composition containing paste-like organosilicon nano- and / or micro-hybrid capsules for scratch and / or abrasion-resistant coatings, which is characterized in that

• a) Oxide particles from the series
  • a) at least one nanoscale oxide and / or mixed oxide of at least one metal or semimetal of the second to sixth main group, the first to eighth subgroup of the periodic table of the elements or the lanthanides or
  • b) a microscale corundum or
  • c) an oxide particle mixture of (a) and (b),
  With
• b) at least one organofunctional silane of the general formula II
  R ¹ _s R ² _r SiY _(4-sr) (II),
  wherein the groups R ¹ and R ^{2 are the} same or different and each have a linear, branched or cyclic alkyl group with 1 to 50 C atoms, an alkenyl group with 2 to 6 C atoms, a chloroalkyl, isocyanoalkyl, cyanoalkyl, fluoroalkyl -, Aryl, acylalkyl, acryloxyalkyl, methacryloxyalkyl, polysulfanalkyl, mercaptoalkyl, thiacyamidalkyl, glycidyloxyalkyl, aminoalkyl, diaminoalkyl, triaminoalkyl, carbonatoalkyl or a ureidoalkyl group, Y represents a methoxy, ethoxy -, i-propoxy, n-propoxy or 2-methoxyethoxy group and s is 1 or 2 or 3 and r is 0 or 1 or 2, with the proviso (s + r) ≦ 3,
  and
• c) optionally a monomeric and / or oligomeric silicic acid ester which carries methoxy, ethoxy, n-propoxy or i-propoxy groups and has an average degree of oligomerization of 1 to 50,
  and
• d) optionally an organofunctional siloxane, its functionalities are the same or different and each Si atom in the siloxane is a functionality from the series alkyl, fluoroalkyl, cyanoalkyl, isocyanoalkyl, alkenyl, aminoalkyl, Diaminoalkyl, triaminoalkyl, alkoxyalkyl, hydroxyalkyl, acylalkyl, Glycidyloxyalkyl, acryloxyalkyl, methacryloxyalkyl, mercaptoalkyl, ureidoalkyl, Aryl or alkoxy and the remaining free valences of the Si atoms in Siloxane are saturated by methoxy or ethoxy or hydroxyl groups,

in situ in a liquid, hardenable synthetic resin or a precursor of a Reacts resin, the content of oxide particles of component (i) 10 to 300 parts by weight, based on 100 parts by weight of the synthetic resin used component, is and the implementation in a kneading or  Dispersing unit, preferably in a Torusmill® under exclusive Use of the dissolver.

When carrying out the process according to the invention, the procedure is preferably such that

• - The hardenable synthetic resin or a precursor of a hardenable synthetic resin in submitted to a kneading or dispersing unit and heated, preferably heated one to 50 to 90 ° C, particularly preferably to 60 to 80 ° C, very particularly preferably to 65 to 75 ° C, in particular to <70 ° C,
• Catalyst, if appropriate adding wetting agent and water,
• - Components (ii) to (iv) and then
• - Add oxide particles (i) with thorough mixing.

It is then convenient to remove those formed during the reaction Alcohol from the system allows the mass to cool down and receives one paste composition according to the invention.

Preferably, the curable is used in the process according to the invention Synthetic resin or precursor of a curable synthetic resin an acrylate, methacrylate, Epoxy, epoxy resin, polyurethane, polyurethane resin, unsaturated polyester, unsaturated polyester resin, epoxy acrylate, polyester acrylate, urethane acrylate, Silicone acrylates or mixtures of two or more of the aforementioned Components.

In particular, but not exclusively, the following compounds can be used as organofunctional silanes according to formula II: methyltrimethoxysilane (DYNASYLAN® MTMS), methyltriethoxysilane (DYNASYLAN® MTES), propyl trimethoxysilane (DYNASYLAN® PTMO), propyltriethoxysilane (DYNASYLANoxylanilyl-PylOnyl) DYNASYLAN® IBTMO), i-butyltriethoxysilane (DYNASYLAN® IBTEO), octyltrimethoxysilane (DYNASYLAN® OCTMO), octyltriethoxysilane (DYNASYLAN® OCTEO), hexadecyltrimethoxysilane (DYNASYLANX) 9-hexane (DYNASYLANX) 3-Jodpropylalkoxysilane, 3-Chlorpropyltrichlorsilane, 3- Chiorpropylmethyldialkoxysilane, 3-Chlorpropylmethyldichlorsilane, 3-Chlorpropyldi methylalkoxysilane, 3-Chlorpropyldimethylchlorsilane, 3-Aminopropylmethyldi alkoxysilanes, 3-aminopropyltrialkoxysilanes, including 3-aminopropyltrimethoxysilane (AMMO DYNASYLAN®), 3-aminopropyltriethoxysilane (DYNASYLAN® AMEO), N- (n-butyl) -3-aminopropyl trimethoxysilane (DYNASYLAN® 1189), n-aminoethyl-3-aminopropylmethyldimethoxysilane (DYNASYLAN® 1411), 3-aminopropyimethyldi ethoxysilane (DYNASYLAN® 1505), N-aminoethyl-3-aminopropylmethyldialkoxysilan (3-amoxynilysilane) (3-aminoxynilysilane), N-amoxynilysilane (3-aminoxynilysilane), N-aminoxysilane (3-aminoxynilysilane) ), tri amino functional propyltrimethoxysilane (DYNASYLAN® TRIAMO), including [N-aminoethyl-N '- (3-trialkoxysilylpropyl)] ethylenediamine and [N-aminoethyl-N- (3-trialkoxysilylpropyl)] ethylenediamine, triaminofunctional propylmethyl , 5-dihydroimidazolyl) propyltriethoxysilane (DYNASYLAN® SYLAN IMEO), 3-meth acryloxypropylalkoxysilane, 3-methacryloxypropyltrimethoxysilane (MEMO DYNASYLAN®), 3-Methacryloxyisobutyltrialkoxysilane, 3-glycidyloxypropyltrialkoxysilanes, 3- glycidyloxypropyltrimethoxysilane (DYNASYLAN ® GLYMO), 3-glycidyloxypropyl triethoxysilane (DYNASYLAN ® GLYEO), 3-glycidyloxypropyl-methyldiethoxysilane, 3-mercaptopropylalkoxysilane, 3-mercaptopropyltrimethoxysilane (DYNASYLAN® MTMO), vinyltrialkoxysil ane, including vinyltrimethoxysilane (VTMO DYNASYLAN®), vinyltriethoxysilane (VTEO DYNASYLAN®), vinyltris (2-methoxyethoxy) silane (VTMOEO DYNASYLAN®) Perfluoralkyltrialkoxysilane, Fluoralkyltrialkoxysilane, including tridecafluorooctyltrimethoxysilane, tridecafluorooctyltriethoxysilane (DYNASYLAN ® F 8261), Tridecafluoroctylmethyldialkoxysilane, trimethylchlorosilane, Triethylchlor silane, (H ₅ C ₂ O) ₃ Si (CH ₂ ) ₃ -S ₄ - (CH ₂ ) ₃ Si (OC ₂ H ₅ ) ₃ 1,4-bis (3-triethoxysilylpropyl) tetrasulfane (Si-69), (H ₅ C ₂ O) ₃ Si (CH ₂ ) ₃ -NCS 3-thiacyamidopropyltriethoxysilane (Si-264), (H ₅ C ₂ O) ₃ Si (CH ₂ ) ₃ -S ₂ - (CH ₂ ) ₃ Si ( OC ₂ H ₅ ) ₃ 1,2-bis (3-triethoxysilylpropyl) disulfane (Si-266), 3-cyanopropyltrialkoxysilane, including 3-cyanopropyltrimethoxysilane, N, N ', N "- tris (trimethoxysilylpropyl) triisocyanurate, 3- [methoxy (polyethylene glycol)] propyltri alkoxysilane, allyltrialkoxysilane, allylmethyldialkoxysilane, allyldimethylalkoxysilane, 3-methacryloxy-2-methylpropyltrialkoxysilane, 3-amino-2-methylpropyltrialkoxy silane, (cycl ohex-3-enyl) -ethyltrialkoxysilane, N- (3-trialkoxysilylpropyl) alkylcarb amate, 3-azidopropyltrialkoxysilane, 4- (2-trialkoxysilylethyl) -1,2-epoxycyclohexane, bis (3-alkoxysilylpropyl) amine, tris (3-alkoxil ) amines, 3-acryloxypropyl trialkoxysilanes, including 3-acryloxymethyldialkoxysilane, 3-acryloxydimethylalkoxysilane, methoxy, ethoxy, 2-methoxyethoxy, propoxy or acetoxy advantageously representing one of the aforementioned alkoxy groups.

According to the invention, component (ii) 3- is particularly preferably Methacryloxypropyltrimethoxysilane, 3-methacryloxypropyltriethoxysilane, 3-meth acryloxypropylmethyldimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, 3- Methacryloxy-2-methyl-propyltrimethoxysilane, 3-methacryloxy-2-methyl-propyltri ethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, vinylmethyldimethoxysilane, Vinylmethyldiethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, n-propyl trimethoxysilane and / or n-propyltriethoxysilane or a mixture of the aforementioned Silanes. A mixture of an n-propylalkoxysilane is particularly preferred and a vinyl alkoxysilane.

According to the invention, component (iv) is preferably an oligomeric one Vinyl trimethoxysilane (DYNASYLAN® 6490), an oligomeric propyl trimethoxysilane oligomeric vinyl trimethoxysilane, an oligomeric 3-methacryloxypropyl trimethoxysilane or a cooligomer from propyltrimethoxysilane and vinyltrimethoxysilane, from 3- Methacryloxypropyltrimethoxysilane and propyltrimethoxysilane, or from 3-methacrylic oxypropyltrimethoxysilane and phenyltrimethoxysilane or from 3-methacryloxypropyl trimethoxysilane and tridecafluoro-1,1,2,2-tetrahydrooctyltriethoxysilane or from 3- Methacryloxypropyltrimethoxysilane and tridecafluoro-1,1,2,2-tetrahydrooctyltri methoxysilane or from vinyltrimethoxysilane and tridecafluoro-1,1,2,2-tetrahydro octyltrimethoxysilane or from vinyltrimethoxysilane and tridecafluoro-1,1,2,2- tetrahydrooctyltriethoxysilane, to give just a few preferred examples. But you can also cooligomerisate, which consist of more than two of the above monomeric organoalkoxysilanes (ii) and (iii) are available, using a such cooligomer preferably at least one vinyl or 3- Methacryloxypropyl group carries.  

In general, the method according to the invention is generally used liquid components of the prepolymer in the kneading or dispersing unit before and heated, gives a defined amount of water, optionally catalyst, optionally wetting agents and the organosilicon components (ii) to (iv) and then introduces component (i) with thorough mixing, for example as a mixture of oxides (a) and (b). That is, suitably one brings first the synthetic resin components, catalyst, wetting agents, water and organosilicon components, optionally other auxiliaries together, mixes and only then is the oxidic component (i) added, with a Component mixture obtained by this method of preparation in particular also characterized by good processing behavior. The one in the implementation Alcohol formed can during the reaction, preferably afterwards, from the Mass to be removed. Subsequently, it is suitably allowed to cool and receives a mass according to the invention.

35 to 200 parts by weight are preferably used in the process according to the invention, particularly preferably 60 to 180 parts by weight, very particularly preferably 80 to 160 parts by weight, in particular <80 to 140 parts by weight, for example 90 to 120 parts by weight, oxidic component of the oxide particles (i) (KA-O), based on 100 parts by weight of the synthetic resin, a.

Components (a) or (b) can be used alone. You use it Mixture (c) of (a) and (b), a weight ratio (a): (b) is preferred from 1:10 to 5: 1. An oxide particle mixture (c) is particularly preferably used a weight ratio of components (a) and (b) from 1: 3 to 1: 1, whole a weight ratio (a): (b) of 1: 2 is particularly preferred.

A nanoscale oxide and / or mixed oxide (a) with an average particle diameter of 1 to 100 nm, particularly preferably from 5 to 50 nm and very particularly preferably from 10 to 40 nm, is preferably used in the process according to the invention. The oxides or mixed oxides can have a BET surface area of 40 to 400 m ² / g, preferably 60 to 250 m ² / g, particularly preferably 80 to 250 m ² / g. As nanoscale oxides or mixed oxides, one can use, for example, but not exclusively, pyrogenic silicic acid, which can be modified by further metal or semimetal components, such as aluminum, titanium, iron or zircon.

The oxidic component (b) is suitably a microscale corundum with an average grain size d ₅₀ of 9 to 15 μm.

It is further preferred that the oxidic component (i) consisting of the Individual components (a) or (b) or (c), and at least one silane-based Component, in particular (ii), (iii) and / or (iv), in a weight ratio of 100: 1 to 0.5: 1, particularly preferably from 10: 1 to 0.5: 1, very particularly preferably from 3: 1 to 1: 1.

As a liquid or hardenable synthetic resin or as a precursor to a liquid, curable resin, d. H. a prepolymer or a mixture of Prepolymers are used, for example, in the process according to the invention Acrylates, methacrylates, epoxies, epoxy resins, polyurethanes, polyurethane resins, unsaturated polyesters, unsaturated polyester resins, epoxy acrylates, Polyester acrylates, urethane acrylates, silicone acrylates, polyfunctional monomers Acrylates, such as trimethylolpropane triacrylate, trimethylolpropane trimethacrylate, ethoxylated trimethylolpropane triacrylate, propoxylated trimethylolpropane triacrylate, Pentaerythritol triacrylate, ethoxylated pentaerythritol tetraacrylate, alkoxylated Tetraacrylates, di-trimethylolpropane tetraacrylates, 3,4-epoxycyclohexane-1-carbon Acid-3,4-epoxycyclohexyl-1'-methyl ester, 1,6-hexanediol diacrylate - by just a few To name examples - or mixtures of two or more of the aforementioned Synthetic resins or prepolymers, for example mixtures of mono- and / or bifunctional or polyfunctional monomers, optionally low-viscosity Acrylates.

The reaction according to the invention generally takes place in the presence of a defined amount of water. Suitably, the per mole of Si  organosilicon components 1 to 6 moles of water.

In the present method, said implementation preferably takes place in Presence of defined amounts of water. One is preferably used per mole hydrolyzable, Si-bonded group of organosilicon components 0.5 up to 6 moles of water, particularly preferably 0.5 to 4 moles of water, very particularly preferably 1 to 2 moles of water.

Furthermore, the reaction according to the invention is preferably in the presence of a Catalyst carried out. An acid is particularly suitable as catalyst, preferably maleic anhydride, maleic acid, acetic acid, acetic anhydride, Glycolic acid, citric acid, methanesulfonic acid, phosphoric acid.

Furthermore, the use of a wetting agent for performing the implementation according to the invention may be helpful. This is how you carry out the implementation preferably in the presence of sodium dodecyl sulfate.

In the process according to the invention, the reaction is preferably carried out at a Temperature in the range of 30 to 100 ° C, preferably at a temperature in Range from 40 to 90 ° C, particularly preferably at 50 to 80 ° C, especially at 60 to 75 ° C carried out.

Hydrolysis and condensation result in the reaction according to the invention usually an alcohol, which one preferably during the reaction and / or then removed from the reaction system. Removing that when implementing alcohol produced can be distilled, suitably under reduced pressure, be performed. As a rule, the alcohol content in the Product mixture, d. H. in the obtained by the implementation of the invention Composition, to <2% by weight, preferably to 0.01 to 1% by weight, particularly preferably reduced to 0.1 to 0.5 wt .-%, so that in advantageously a solvent-free composition, i. H. a solvent-free Receives paste.  

Compositions according to the invention are used in particular as Additive or as a basic component for the production of a Coating composition or a lacquer for producing scratch and / or abrasion-resistant coatings.

In general, compositions according to the invention can be used for the Use production of coating agents and radical, thermal and / or Harden photo- or radiation-chemically.

The composition according to the invention or the add other components, such as initiators, to the paint available from it for UV or photochemical curing, Darocur® 1173, Lucirin® TPO-L, Paint stabilizers such as HALS compounds, Tinuvine® and antioxidants such as Irganox®. Such additives are generally used in amounts of 0.1 to 5% by weight, preferably from 2 to 3% by weight, based on the preparation or the lacquer, used. Additional components are introduced into the coating system suitably with thorough mixing. The invention Preparations or varnishes are advantageous despite a high content organosilicon nano or micro hybrid capsules preferably by a comparatively low viscosity from 500 to 1000 mPa.s. Behave in the process the systems are usually dilated.

The invention thus also relates to the use of an inventive containing pasty organosilicon nano and / or micro hybrid capsules Composition for the preparation of a lacquer for producing scratch and / or abrasion-resistant coatings.

The use according to the invention is also an object of the invention Production of the lacquer the pasty organosilicon nano and / or Composition containing micro-hybrid capsules with a liquid synthetic resin, a precursor compound of a synthetic resin and / or a solvent in diluted easily and economically with stirring.  

The application of the said composition or one made from it or modified lacquers is usually applied to a substrate. For The coating of substrates can be done using the usual coating methods apply such. B. roller application, knife application, dipping, flooding, pouring, spraying, Brushing.

For example, you can paint on web-shaped substrates such as paper or Metal or plastic films, evenly by using a roller applicator apply and then harden. But it has also been shown that the solvent-free paint without the addition of solvents with conventional spray technology in the Spray process can be processed. This makes it possible to have three-dimensional To coat and harden substrates. Suitably you can Coating at ambient temperature, d. H. Paint temperature, by a UV or Electron beam process (ESH) cure in an environmentally friendly way because it is solvent-free.

Preferably, electrons with an energy of approx. 140 keV, the dose being 30 to 60 kGy, preferably 40 to 50 kGy. The residual O ₂ content is preferably <200 ppm. The photochemical curing is suitably carried out under a protective gas, for example under nitrogen or argon.

However, lacquer curing can also be carried out by means of UV radiation using mono- or polychromatic UV lamps with a wavelength of 150 to 400 nm. UV curing can also be carried out at ambient temperature, for example between 10 and 60 ° C. Here, too, the O ₂ content is suitably <200 ppm.

So you can by using such a paint in a particularly advantageous How to produce excellent scratch and abrasion resistant coatings. The The scratch hardness or scratch resistance is usually determined in accordance with DIN 53 799 using a hard metal ball. The abrasion can for example according to DIN 52 347 using coated face plates.  

Coatings according to the invention preferably have a layer thickness of 2 to 100 microns, particularly preferably from 5 to 50 microns and very particularly preferred from 5 to 20 µm.

So you can, for example, in a particularly simple and economical manner Metals, such as aluminum, iron, steel, brass, copper, silver, magnesium, Light metal alloys, wood, paper, cardboard, textiles, stone goods, plastics, Thermoplastics, polycarbonate, glass, ceramics, with a particularly scratch and Equip abrasion-resistant coating. The selection of the essentially fixed Substrate materials for coating are unlimited. Such substrates can for example with a UV and weather-resistant protective coating be equipped, so-called "top coating", such as as Clear coat system is used in the automotive industry.

In particular, following such a coating process are simpler and Economically scratch-resistant or abrasion-resistant articles, such as decorative paper, Aluminum foils, polycarbonate car windows, PVC window frames, doors, Countertops, flooring, parquet floors, to name a few, available.

The following examples illustrate the present invention:

Examples feedstocks

Ebecryl® EB 1290: hexafunctional aliphatic urethane acrylate from UCB Chemicals.
Ebecryl® EB 5129: Mixture of aliphatic urethane hexaacrylate and pentaerythritol tri / tetraacrylate from UCB Chemicals.
CN 936: aliphatic urethane diacrylate from Cray Valley.
DPGDA: dipropylene glycol diacrylate from UCB Chemicals.
HDDA: 1,6-hexanediol diacrylate from UCB Chemicals.
SR 444: Mixture of pentaerythritol tri and tetraacrylate from Cray Valley.
DYNASYLAN® VTMO: vinyl trimethoxysilane from Degussa AG.
DYNASYLAN® 6490: Mixture of oligomeric vinyl trimethoxysilanes with a degree of oligomerization of 2 to 12 condensate from Degussa AG.
Plakor® 13: synthetic corundum (corundum micropowder, d ₅₀

= 13 µm) from ESK-SIC GmbH.
AEROSIL® OX 50: fumed silica (amorphous, BET 50 m ²

/ g, d ₅₀

= 30 nm).
AEROSIL® 200: fumed silica (amorphous, BET = 200 m ²

/ g, d ₅₀

= 30 nm) the Degussa AG.

example 1 Preparation of the paste

In a laboratory kneader (Werner and Pfleiderer) 3 kg CN936 and 9.1 g 4-Hydroxyanisole submitted and heated to 60 to 65 ° C. To the heated acrylate were a solution of 90 g within 5 minutes with intensive kneading Maleic anhydride in 0.75 kg water and 3 kg within 30 minutes DYNASYLAN® VTMO given. Then metered in the above Temperature range under continuous kneading 3 kg AEROSIL® OX50 within of an hour. For extensive hydrolytic condensation of the silane and to remove methanol / water, the kneading process was set at 65 to 70 ° C continue for 2 hours under reduced pressure (approx. 50 to 100 torr). Most recently the mixture cooled to room temperature.

Production of the ready-to-use paint

1 kg of SR444 was heated to approximately 40 ° C. in a stirred vessel. Then wore one at this temperature with constant vigorous stirring within 30 minutes, 667 g of the paste obtained above. After another hour The mixture was cooled to room temperature while stirring.  

Example 2 Preparation of the paste

In a laboratory kneader (company Werner and Pfleiderer) 3 kg EB1290 as well 9.5 g of 4-hydroxyanisole are introduced and heated to 60 to 65 ° C. For warmed up Acrylate became a solution within 5 minutes with intensive kneading 28.5 g maleic anhydride in 0.26 kg water and within 30 minutes 0.949 kg DYNASYLAN® VTMO given. Then you metered in the above specified temperature range with continuous kneading 1.323 kg Plakor® 13 and 1.853 kg AEROSIL® OX50 within one hour. For the most part hydrolytic condensation of the silane and removal of methanol / water set the kneading process at 65 to 70 ° C for 2 hours under reduced Pressure (approx. 50 to 100 torr). Finally the approach was to room temperature cooled.

Production of the ready-to-use paint

1.412 kg of DPGDA were heated to approximately 40 ° C. in a stirred vessel. Subsequently were worn at this temperature with constant vigorous stirring inside of an hour, the total amount of the paste obtained above. After another the mixture was cooled to room temperature for one hour.

Comparative example to example 2

15.78 kg of EB 1290 and 7.43 kg of DPGDA and 48 g of 4- Hydroxyanisole submitted and heated to 65 to 70 ° C. To the heated acrylate were a solution of 0.15 kg maleic anhydride in 1.364 kg water as well given 4.988 kg of DYNASYLAN® VTMO within 30 minutes. Subsequently were metered in the temperature range given above with vigorous stirring 6.96 kg Plakor® 13 and 9.74 kg AEROSIL © OX 50 within one hour. you stirred for a further 1 hour at 65 to 70 ° C and then distilled in vacuo methanol formed by the hydrolysis of the silane. The approach was last cooled to room temperature.  

Example 3 Preparation of the paste

11.22 kg of Ebecryl® 5129 were placed in a Torusmill® 20 C (VMA-Getzmann GmbH) as well as 43.2 g of 4-hydroxyanisole and with stirring (typically 500 to 1000 rpm, dissolver) heated to 75 ° C. For the heated acrylate Solution of 135 g maleic acid in 0.81 kg water and within 5 to 10 Minutes 2.98 kg of DYNASYLAN® 6490. Then one metered at above temperature and 1000 to 2000 rpm stirring speed (Dissolver) 5.97 kg AEROSIL® 200 such that the reaction mixture is still good remained stirrable, which required 3 to 4 hours of dosing. In the second half of the time the AEROSIL dosage was also an intermittent addition of HDDA required to ensure stirring, a total of 3.3 kg HDDA used. The mixture was stirred for a further 2 hours at 75 ° C. and 2000 using a dissolver up to 3000 rpm, converted the still flowable paint into a suitable one Jar and allowed to cool to room temperature, allowing gradual solidification of a pasty mass.

Production of the ready-to-use lacquer from that produced according to Example 3 Paste:

Example 3.1

0.374 kg of HDDA were heated to about 40 ° C. in a stirred vessel. Subsequently were worn at this temperature with constant vigorous stirring inside 1 kg paste over 30 minutes. After stirring for another hour, the Approach cooled to room temperature.

Example 3.2

0.279 kg of HDDA were heated to about 40 ° C. in a stirred vessel. Subsequently were worn at this temperature with constant vigorous stirring inside  1 kg paste over 30 minutes. After stirring for another hour, the Approach cooled to room temperature.

Example 3.3

0.209 kg of HDDA were heated to approximately 40 ° C. in a stirred vessel. Subsequently were worn at this temperature with constant vigorous stirring inside 1 kg paste over 30 minutes. After stirring for another hour, the Approach cooled to room temperature.

Example 4

11.22 kg of Ebecryl® 1290 were placed in a Torusmill® 20 C (VMA-Getzmann GmbH) as well as 43.2 g of 4-hydroxyanisole and with stirring (typically 500 to 1000 rpm. Dissolver) heated to 75 ° C. For the heated acrylate Solution of 135 g maleic acid in 0.81 kg water and within 5 to 10 minutes 2.98 kg DYNASYLAN® 6490 given. Then one metered in the above-mentioned temperature and 1000 to 2000 rpm stirring speed (Dissolver) 5.97 kg AEROSIL® 200 such that the reaction mixture is still good remained stirrable, which required 3 to 4 hours of dosing. In the second half of the time the AEROSIL dosage was also an intermittent addition of HDDA required to ensure stirring, a total of 3.3 kg HDDA used. The mixture was stirred for a further 2 hours at 75 ° C. and 2000 to 3000 rpm using a dissolver, converted the still flowable paint into a suitable one Jar and allowed to cool to room temperature, allowing gradual solidification of a pasty mass.

Production of the ready-to-use lacquer from that produced according to Example 4 Paste:

Example 4.1

0.498 kg of HDDA were heated to approximately 40 ° C. in a stirred vessel. Subsequently  were worn at this temperature with constant vigorous stirring inside 1 kg paste over 30 minutes. After stirring for another hour, the Approach cooled to room temperature.

Example 4.2

0.372 kg of HDDA were heated to about 40 ° C. in a stirred vessel. Subsequently were worn at this temperature with constant vigorous stirring inside 1 kg paste over 30 minutes. After stirring for another hour, the Approach cooled to room temperature.

Example 4.3

0.279 kg of HDDA were heated to about 40 ° C. in a stirred vessel. Subsequently were worn at this temperature with constant vigorous stirring inside 1 kg paste over 30 minutes. After stirring for another hour, the Approach cooled to room temperature.

applications

The ready-to-use lacquers from Examples 1, 2, 3.1 to 3.3, 4.1 to 4.3 and from the comparative example were used to determine the abrasion Decor paper with a squeegee with a gap width of 25 µm and to determine the Scratch hardness on square PVC sheets (edge length 10 cm, thickness 2 mm) with a Doctor blade with a gap width of 50 µm and applied in low-energy Electron accelerator (140 keV) cured with a dose of 50 kGy. The The residual oxygen content in the accelerator was <200 ppm.

The samples were scratched according to DIN 53 799 using a Diamond tip and a carbide ball tested. The samples were also on Abrasion resistance according to DIN 68 861 using emery paper S-42, 2 friction wheels CS-0 tested at 50 and 1000 revolutions. Furthermore, were Samples tested according to DIN 52 347 (Haze) and D-1044 (ASTM). The respective  Test results are summarized in Tables 1 and 2.

Table 1

Compilation of the test results

Table 2

Claims (22)

1. Highly filled composition containing paste-like organosilicon nano and / or micro hybrid capsules for scratch and / or abrasion resistant coatings,
wherein an organosilicon nano or micro hybrid capsule consists of an oxidic core A, which contains at least one nanoscale or microscale oxide particle (KA-O) of components (a) and / or (b), and an organosilicon coating B and the organosilicon coating B at least one organosilicon component of the general formula 1a
(Si'O-) _x Si-R (1a),
wherein R stands for an organofunctional group and x is a number from 0 to 20, the still free valences of Si saturated by SiO- and / or -Z and the free valences of Si 'by SiO-, -R and / or -Z the groups Z are identical or different and represent hydroxyl or alkoxy radicals, and each Si or Si 'of the coating B bears a maximum of one group R,
contains and / or the organosilicon component of the coating B via one or more covalent bonds of the general formula Ib
(KA-O) - [(Si'O-) _x Si-R] (Ib),
where R has the meaning given above and x is a number from 0 to 20, the free valences of Si by (KA-O) -, SiO- and / or -Z and the free valences of Si 'by (KA-O ) -, SiO-, -R and / or -Z are saturated, the groups Z are the same or different and represent hydroxyl or alkoxy radicals, and each Si or Si 'of the coating B carries at most one group R,
is bound to the core A (KA-O),
available through an implementation of

• a) Oxide particles from the series
  • a) at least one nanoscale oxide and / or mixed oxide of at least one metal or semimetal of the second to sixth main group, the first to eighth subgroup of the periodic table of the elements or the lanthanides or
  • b) a microscale corundum or
  • c) an oxide particle mixture of (a) and (b),
  With
• b) at least one organofunctional silane of the general formula II
  R ¹ _s R ² _r SiY _(4-sr) (II),
  wherein the groups R ¹ and R ^{2 are the} same or different and each have a linear, branched or cyclic alkyl group with 1 to 50 C atoms, an alkenyl group with 2 to 6 C atoms, a chloroalkyl, isocyanoalkyl, cyanoalkyl, fluoroalkyl -, Aryl, acylalkyl, acryloxyalkyl, methacryloxyalkyl, polysulfanalkyl, mercaptoalkyl, thiacyamidalkyl, glycidyloxyatkyl, aminoalkyl, diaminoalkyl, triaminoalkyl, carbonatoalkyl or a ureidoalkyl group, Y represents a methoxy, ethoxy -, i-propoxy, n-propoxy or 2-methoxyethoxy group and s is 1 or 2 or 3 and r is 0 or 1 or 2, with the proviso (s + r) ≦ 3,
  and
• c) optionally a monomeric and / or oligomeric silicic acid ester which carries methoxy, ethoxy, n-propoxy or i-propoxy groups and has an average degree of oligomerization of 1 to 50,
  and
• d) optionally an organofunctional siloxane, the functionalities of which are the same or different and each Si atom in the siloxane is a functionality from the series alkyl, fluoroalkyl, cyanoalkyl, isocyanoalkyl, alkenyl, aminoalkyl, diaminoalkyl, triaminoalkyl, alkoxyalkyl, hydroxyalkyl, acylalkyl, glycidyloxyalkyl, acryloxyalkyl , Methacryloxyalkyl, mercaptoalkyl, ureidoalkyl, aryl or alkoxy and the remaining free valences of the Si atoms in the siloxane are saturated by methoxy or ethoxy or hydroxyl groups,
  wherein the reaction takes place in situ in a liquid, curable synthetic resin or a precursor stage of a synthetic resin, the content of oxide particles of component (i) is 10 to 300 parts by weight, based on 100 parts by weight of the synthetic resin component used, and the Implemented in a kneading or dispersing unit.

2. A method for producing a paste-like composition containing organic silicon nano and / or micro hybrid capsules for scratch and / or abrasion resistant coatings according to claim 1, characterized in that

• a) Oxide particles from the series
  • a) at least one nanoscale oxide and / or mixed oxide of at least one metal or semimetal of the second to sixth main group, the first to eighth subgroup of the periodic table of the elements or the lanthanides or
  • b) a microscale corundum or
  • c) an oxide particle mixture of (a) and (b),
  With
• b) at least one organofunctional silane of the general formula II
  R ¹ _s R ² _r SiY _(4-sr) (II),
  wherein the groups R ¹ and R ^{2 are the} same or different and each have a linear, branched or cyclic alkyl group with 1 to 50 C atoms, an alkenyl group with 2 to 6 C atoms, a chloroalkyl, isocyanoalkyl, cyanoalkyl, fluoroalkyl -, Aryl, acylalkyl, acryloxyalkyl, methacryloxyalkyl, polysulfanalkyl, mercaptoalkyl, thiacyamidalkyl, glycidyloxyalkyl, aminoalkyl, diaminoalkyl, triaminoalkyl, carbonatoalkyl or a ureidoalkyl group, Y represents a methoxy, ethoxy -, i-propoxy, n-propoxy or 2-methoxyethoxy group and s is 1 or 2 or 3 and r is 0 or 1 or 2, with the proviso (s + r) ≦ 3,
  and
• c) optionally a monomeric and / or oligomeric silicic acid ester which carries methoxy, ethoxy, n-propoxy or i-propoxy groups and has an average degree of oligomerization of 1 to 50,
  and
• d) optionally an organofunctional siloxane, the functionalities of which are the same or different and each Si atom in the siloxane is a functionality from the series alkyl, fluoroalkyl, cyanoalkyl, isocyanoalkyl, alkenyl, aminoalkyl, diaminoalkyl, triaminoalkyl, alkoxyalkyl, hydroxyalkyl, acylalkyl, glycidyloxyalkyl, acryloxyalkyl , Methacryloxyalkyl, mercaptoalkyl, ureidoalkyl, aryl or alkoxy and the remaining free valences of the Si atoms in the siloxane are saturated by methoxy or ethoxy or hydroxyl groups,
  implemented in situ in a liquid, curable synthetic resin or a precursor of a synthetic resin, the content of oxide particles of component (i) is 10 to 300 parts by weight, based on 100 parts by weight of the synthetic resin component used, and the reaction is carried out in one Kneading or dispersing unit.

3. The method according to claim 2, characterized, that as a hardenable synthetic resin or precursor of a hardenable Synthetic resin an acrylate, methacrylate, epoxy, epoxy resin, polyurethane, Polyurethane resin, unsaturated polyester, unsaturated polyester resin, Epoxy acrylate, polyester acrylate, urethane acrylate, silicone acrylates or mixtures uses two or more of the aforementioned components. 4. The method according to claim 2 or 3, characterized, that <80 to 200 parts by weight of the oxidic component (i), based on 100 parts by weight of the synthetic resin used. 5. The method according to any one of claims 2 to 4, characterized, that the oxidic components (i) and at least one silane-based Component (ii), (iii) and / or (iv) in a weight ratio of 100: 1 to 0.5: 1. 6. The method according to any one of claims 2 to 5, characterized, that as component (a) at least one nanoscale oxide and / or Mixed oxide from the series of elements Si, Al, Ti and / or Zr is used and the Particles have an average grain size of 1 to 200 nm. 7. The method according to any one of claims 2 to 6, characterized, that a nanoscale silica is used as component (a).   8. The method according to any one of claims 2 to 7, characterized, that as component (b) a microscale corundum with a medium Grain size from 3 to 40 microns. 9. The method according to any one of claims 2 to 8, characterized, that as component (c) an oxide particle mixture consisting of a uses nanoscale silica (a) and a microscale corundum (b). 10. The method according to any one of claims 2 to 9, characterized, that as component (ii) 3-methacryloxypropyltrimethoxysilane, 3- Methacryloxypropyltriethoxysilane, 3-methacryloxypropyfmethyldimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, 3-methacryloxy-2-methyl-propyltri methoxysilane, 3-methacryloxy-2-methyl-propyltriethoxysilane, vinyltrimethoxy silane, vinyltriethoxysilane, vinylmethyldimethoxysilane, vinylmethyldiethoxysilane, Phenyltrimethoxysilane, phenyltriethoxysilane, n-propyltrimethoxysilane or n- Propyltriethoxysilane or a mixture of two or more of the above called silanes. 11. The method according to any one of claims 2 to 10, characterized, that as component (iv) at least one n-propylmethoxysiloxane, n- Propylethoxysiloxane, vinylmethoxysiloxane, vinylethoxysiloxane, phenyltrimeth oxysiloxane, phenyltriethoxysiloxane, perfluoro-1,1,2,2-tetrahydroalkylethoxy siloxane and perfluoro-1,1,2,2-tetrahydroalkylmethoxysiloxane, each with 3 to 16 carbon atoms in the alkyl groups, 3-methacryloxypropylmethoxysiloxane, 3- Methacryloxypropylethoxysiloxane, n-propynyl methoxysiloxane, n-propyl / - Vinylethoxysiloxane, phenyl / vinylethoxysiloxane, phenyl / vinylmethoxysiloxane, 3- Methacryloxypropyl / n-propylmethoxysiloxane, 3-methacryloxypropyl / n-propyl ethoxysiloxane, 3-methacryloxypropyl / phenylmethoxysiloxane, 3-methacryloxy  propyl / phenylethoxysiloxane, 3-methacryloxypropyl / tridecafluoro-1,1,2,2-tetra hydrooctylmethoxysiloxane, 3-methacryloxypropyl / tridecafluoro-1,1,2,2-tetra hydrooctylethoxysiloxane, vinyl / tridecafluoro-1,1,2,2-tetrahydrooctylmethoxy siloxane, vinyl / tridecafluoro-1,1,2,2-tetrahydrooctylethoxysiloxane or one Mix of them. 12. The method according to any one of claims 2 to 11, characterized, that one carries out the reaction in the presence of a catalyst. 13. The method according to any one of claims 2 to 12, characterized, that the reaction is carried out in the presence of a wetting agent. 14. The method according to any one of claims 2 to 13, characterized, that the reaction is carried out in the presence of water. 15. The method according to any one of claims 2 to 14, characterized, that 0.5 to 6 moles per mole of Si of the organosilicon component (ii) Water begins. 16. The method according to any one of claims 2 to 15, characterized, that the reaction at a temperature in the range of 30 to 100 ° C. performs. 17. The method according to any one of claims 2 to 16, characterized in that

• - the curable synthetic resin or a precursor of a curable synthetic resin is placed in a kneading or dispersing unit and heated,
• Catalyst, if appropriate adding wetting agent and water,
• - Components (ii) to (iv) and then
• - Add oxide particles (I) with thorough mixing.

18. The method according to claim 17, characterized, that the hardenable synthetic resin or a precursor compound of one curable synthetic resin to a temperature in the range of 50 to 90 ° C. heated. 19. The method according to claim 16 or 17, characterized, that the hardenable synthetic resin or a precursor compound of one curable resin to a temperature in the range of 65 to 75 ° C. heated. 20. The method according to any one of claims 2 to 19, characterized, that during the implementation and / or afterwards the resulting alcohol removed from the reaction system. 21. Use of a pasty organosilicon nano and / or Microhybrid capsule-containing composition according to claim 1 or a corresponding composition which according to one of claims 2 to 20 is produced for the production of a lacquer for producing scratch-resistant and / or abrasion resistant coatings. 22. Use according to claim 21, wherein to produce the lacquer containing pasty organosilicon nano and / or micro hybrid capsules Composition with a liquid synthetic resin, a precursor compound a synthetic resin and / or a solvent.