WO2013139599A1

WO2013139599A1 - Method for producing an anticorrosive coating

Info

Publication number: WO2013139599A1
Application number: PCT/EP2013/054473
Authority: WO
Inventors: Stefan Sepeur; Stefan Goedicke; Martin Muennich; Alexandra MUTH
Original assignee: Nano-X Gmbh
Priority date: 2012-03-22
Filing date: 2013-03-06
Publication date: 2013-09-26
Also published as: DE102012005806A1; EP2828007A1

Abstract

The present invention relates to a method for producing an anticorrosive coating on a substrate and to an anticorrosive coating that can be obtained by this method.

Description

Process for the preparation of a corrosion protection coating

The present invention relates to a process for producing a corrosion protection coating on a substrate and to a corrosion protection coating obtainable by this process.

Anti-corrosive coatings and coating agents for producing such coatings are known in the art. For example, DE 10 2004 034 645 A1 discloses a corrosion protection coating composition for metal comprising an organic binder with an organosilicon compound and a particulate metal. Organosilicon compounds proposed are polyorganosiloxane resins and, in particular, silicon-modified epoxy resin. The coating agent is applied to the workpiece in liquid form and precrosslinked at a temperature of 130 ° C. over a period of 30 minutes. Subsequently, the first layer thus obtained is provided with a black Epoxidharzpulverlack as a topcoat and both layers are cured together at a temperature of 160 ° C to 200 ° C.

CA 2,560,335 A1 also discloses an anticorrosive coating containing a binder of condensed silanes with epoxy, mercaptan or hydroxyalkyl groups. The binder is mixed with metal particles and predried after application to a substrate for 10 minutes at 80 ° C or cured for 30 minutes at 300 ° C. Subsequently, the first layer is provided with another epoxysilane-based coating and both layers are cured together at 150 ° C for 20 minutes.

DE 10 2006 003 956 proposes a method for producing an anticorrosive coating, wherein first a sol-gel film is applied and cured, and then at least one further layer is applied.

The methods known in the prior art for the production of anticorrosive coatings have the disadvantage that the first layer must first be precured for at least 10 minutes at elevated temperatures in the range of 80 ° C to 130 ° C before the cover and protective layer are applied can. As a result, the application of appropriate anticorrosive coatings time and energy consuming and therefore associated with undesirably high costs, especially in mass production. In addition, the construction of the known anticorrosion coatings of two layers of different chemical composition, of which the first layer is first at least partially cured before the second layer is applied, results in the coating as a whole not having the desired protective effect under all conditions. For example, the known anticorrosive coatings have insufficient resistance to chemicals and especially detergents.

An object of the present invention is to overcome the mentioned disadvantages of the prior art. In particular, a corrosion protection coating is to be made available, which can be produced quickly and with the least possible expenditure of energy and which is constructed such that the upper cover and protective layer protects the underlying first metal-particle-containing corrosion protection layer particularly effectively, for example against environmental influences or the attack of chemicals. In addition, the corrosion protection coating should have a high hardness and thus resistance to mechanical wear or damage.

It has now surprisingly been found that these objects can be achieved by curing the first, metal particle-containing layer and the second layer simultaneously in the presence of a metal alkoxide as a curing catalyst.

The present invention thus relates to a method for producing a corrosion protection coating on a substrate, comprising the steps:

a) applying a first coating agent to the substrate, the first coating agent containing epoxy-modified silica, a curing catalyst, solvent and metal particles to obtain a first layer;

b) applying a second coating agent to the first layer, the second coating agent containing epoxy-modified silica, a curing catalyst and solvent to obtain a second layer;

c) simultaneously curing the first and second layers; characterized in that the curing catalyst used in the first and second Besc ichtungsmittel a metal alkoxide, wherein the metal alkoxide is not silicon alkoxide.

It has been found that by using a metal alkoxide as a curing catalyst, both layers can be cured simultaneously and rapidly at a relatively low temperature. It is therefore no longer necessary, in contrast to the prior art, at least partially precuring the first layer before applying the second layer, but the second layer can be applied to the first layer immediately or after brief drying. As a result, the overall process for producing the anticorrosive coating is substantially accelerated and, moreover, it is not necessary to heat the substrate coated with the first layer and then to cool it again before applying the second layer, so that both energy and time are saved. In addition, the metal alkoxide hardening catalyst in both layers enables simultaneous curing of the two layers at a comparatively low temperature of, for example, only about 110 ° C.

In addition, it has been found that when both layers contain an epoxy-modified silica as a binder and a metal alkoxide curing catalyst, and both layers are cured simultaneously, the resulting anti-corrosion coating is particularly insensitive to environmental or chemical influences. For example, it has been found that a brake disk provided with the anticorrosion coating according to the invention also has a substantially greater contact with commercial rim cleaners, which apparently permeate the cover and protective layer of corrosion protection coatings known from the prior art and can attack the underlying metal particle-containing anticorrosion layer Resistant. In addition, the corrosion protection coating obtainable by the process according to the invention is particularly stable to mechanical influences, such as scratching.

As the curing catalyst, both the first and second coating agents contain a metal alkoxide. Depending on the epoxy-modified silicon dioxide used and the desired curing time and temperature, suitable metal alkoxides may be used Be chosen professional. The two coating compositions may contain identical or different metal alkoxides as curing catalysts. Both coating compositions preferably contain the same metal alkoxide.

As curing catalysts, in particular, alkoxides of aluminum, titanium, zirconium, tantalum, niobium, tin, zinc and tungsten are suitable, wherein as alkoxides preferably CI_ ₁₀ -, in particular C ^ alkoxy groups are present.

Examples of suitable curing catalysts are zirconium isopropylate, zirconium n-propylate, zirconium tert-butoxide, tantalum ethanolate, tantalum tert-butylate, niobium ethoxide, niobium tert-butylate, tin tert-butoxide, tungsten ( VI) ethanolate, germanium ethanolate, germanium iso-propylate, titanium (IV) methoxide, titanium (IV) ethoxide, titanium (IV) sec-butoxide, titanium (IV) t-butoxide, titanium (IV) isobutylate, Titanium (IV) isopropylate, titanium (IV) n-propylate, titanium (IV) -2-ethylhexyl oxide, titanium (IV) (triethanolaminato) isopropoxide, titanium diisopropoxide bis (acetylacetonate), dibutyl triethanolamine titanate, tetraphenyl titanate, tetrahexyl titanate, titanium (IV) -2-propenolate, tetrakis (l -ethylpropyl) titanate, tetrapentyl titanate, tetrakis (1,1-dimethylpropyl) titanate, tetrakis (3-methylbutyJ) titanates, tetrakis (1, 1-dimethylbuty)) titanates, Tetrakis (1-methyl-1-ethylpropyl) titanates, aluminum methoxide, aluminum ethylate, aluminum n-propylate, aluminum isopropylate, aluminum n-butoxide, aluminum sec-butoxide, Alu minium tert-butoxide, aluminum isobutylate, aluminum butoxyethoxide,

Zirconium ethoxide, tetra-n-butyl icirconate, tetra-sec-butyl zirconate, tetra-tert-butyl zirconate, zirconium tetrakis (1,1-dimethyl propoxide) and tetrapentyl zirconate.

Particularly in the case of particularly reactive alkoxides, for example of aluminum, titanium or zirconium, it may be advisable to use them in complexed form. Here, for example, unsaturated carboxylic acids and beta-dicarbonyl compounds, such as methacrylic acid, acetylacetone and ethyl acetoacetate, suitable complexing agents.

Particularly preferred curing catalysts according to the invention are aluminum butoxyethanolate and an aluminum acetylacetonate complex.

Particularly chemical resistant anticorrosive coatings are obtained by the process according to the invention when the first and the second coating agent contain the same epoxy-modified silicon dioxide and the same Curing catalyst included. As a result, a particularly uniform curing of the first and second layer is achieved. In addition, both layers have similar chemical compositions after curing, so that the upper cover and protective layer can protect the underlying metal particle-containing corrosion protection layer particularly effective.

The amount of the curing catalyst used in each of the two Beschi treatment is not particularly limited and depends on the desired curing time and temperature. For example, each of the two layers may contain the curing catalyst in an amount of 0.5-20 wt.% Based on the weight of epoxy-modified silica in the particular coating agent.

Suitable epoxy-modified silica binders are known to the person skilled in the art and can be obtained, for example, by condensation of epoxy-modified alkoxysilane. Corresponding Kondenstionsreaktionen are known as sol-gel method. In this process, the hydrolyzable alkoxy groups of the alkoxysilanes used are cleaved off, the silanes condensing to form silica sols. The epoxy modifications contained in the alkoxysilanes used are excluded from this condensation reaction, so that epoxy-modified silica sols are formed. The alkoxy radicals are split off during the condensation and are released as alcohol into the reaction solution.

The epoxy-modified silica can be prepared either exclusively from said epoxy-modified alkoxysilanes or from a mixture of epoxy-modified alkoxysilanes with other, non-epoxy-modified silanes, especially alkoxysilanes, such as phenylethyltrimethoxysilane, phenylethyltriethoxysilane, phenylmethyldiethoxysilane, phenyldimethylethoxysilane, 3-aminopropyltriethoxysilane (APTES), aminoethylaminopropylsilane, 3 -

Aminopropyltrimethoxysilane (APTMS), N- (2-aminoethyl) -3-aminopropyltrimethoxysilane (DIAMO), N- (2-aminoethyl) -3-aminopropylmethyldimethoxysilane, N-cyclohexyl-3-aminopropyltrimethoxysilane, benzylaminoethylaminopropyltrimethoxysilane, vinylbenzylaminoethylaminopropyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane (VTEOS) , Vinyldimethoxymethylsilane, vinyl (tris) methoxyethoxy) silane,

Vinylmethoxymethylsilane, vinyltris (2-methoxyethoxy) silane, vinyltriacetoxysilane, mercaptopropyltrimethoxysilane, bis-triethoxysilylpropyldisulfidosilane, bis- Triethoxysilylpropyltetrasulfidosilan, N-Cyclohexylaminomet yldiethoxysilane, N-cyclohexylaminomethyltriethoxysilane, N-phenylaminomethyltrimethoxysilane, N-phenylaminopropyltrimethoxysilane (methacryloxymethyl) methyldimethoxysilane ₁ methacryloxymethyltrimethoxysilane, (methacryloxymethyl) methyldiethoxysilane, methacryloxymethyltriethoxysilane, 3-Methacryloxypropyltrimet oxysilane, 3-

Methacryloxypropyltriacetoxysilane, (isocyanatomethyl) methyldimethoxysilane, 3-isocyanatopropyltrimethoxysilane, (ICTMS), 3-isocyanatopropyltriethoxysilane, 3-trimethoxysilyl \ y \ methyl \ -0-metycarbamate, ND \ metoxy (melhyi) si \ y \ met y ] -0-met y] carbamate, 3- (triethoxysilyl) propylsuccinic anhydride, aminopropylmethyldiethoxysilane, aminopropylmethyimethoxysilane, 1,2-bis (triethoxysilyl) ethane, bis-3- (triethoxypropylsilyl-propyl) amine, bis-3- (trimethoxypropylsilylpropyl) amine, butylaminopropyltrimethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltriethoxysilane, N-ethyl-3-aminoisobutyltrimethoxysilane, ethyltriacetosilane (ETA ), 3-isocyanatopropyltriethoxysilane (ICTES), methyltriacetoxysilane, mercaptopropyltriethoxysilane, mercaptopropyltrimethoxysilane, N-

Methylaminopropyltrimethoxysilane, 3- (2- (2- aminoethylamino) ethylamino) propyltriethoxysilane (TRIAMO), tris (3-trimethoxysilylpropyl isocyanurate), Octadecylaminodimethyltrimethoxysilylpropylammoniumchlorid, 3- methacryloxypropylmethyldimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, 3-methacryloxypropyltriethoxysilane, 3- acryloxypropyltrimethoxysilane, N- (2-aminoethyl) -3-aminopropyltriethoxysilane, 3-triethoxysilyl-N- (1,3-dimethyl-butylidene) propylamine, N-phenyl-3-aminopropyltrimethoxysilane, 3-ureidopropyltriethoxysilane, 3-chloropropyltrimethoxysilane, 3-mercaptopropylmethyldimethoxysilane, 3 Mercaptopropyltrimethoxysilane, bis (triethoxysilylpropyl) tetrasulfide, tetraethoxysilane, methyltrimethoxysilane,

Methyltriethoxysilane, dimethyldimethoxysilane, hexyltrimethoxysilane, hexyltriethoxysilane, decyltrimethoxysilane, ethyltrimethoxysilane, ethyltriethoxysilane, propyltrimethoxysilane, propyltrimethoxysilane, methyltrimethoxysilane, ethyltrimethoxysilane, n-hexyltrimethoxysilane, n-octyltriethoxysilane, n-octyltrimethoxysilane, propyltrimethoxysilane, propyltriethoxysilane, t-butyltrimethoxysilane, phenyltrimethoxysilane, phenyltriethoxysilane, isobutyltriethoxysilane (IBTEO) , Isobutyltrimethoxysilane (IBTEO), tetraethoxysilane (TEOS), methyltriethoxysilane (MTEOS), dimethyldimethoxysilane, dimethyldiethoxysilane (DMDES), trimethylethoxysilane, isooctyltrimethoxysilane, isooctyltriethoxysilane, hexadecyltrimethoxysilane,

(Octadecyl) methyldimethoxysilane, (cyclohexyl) methyldimethoxysilane, dicyclopentyldimethoxysilane and hexadecyltriethoxysilane. In addition, either already during the condensation of the alkoxysilanes or later additionally pre-condensed silica may be added, for example in the form of silica sol or silica.

In order to achieve a good curing of the layers, the epoxy-modified silica used in both coating compositions should in each case contain 0.5-10 mol, preferably 1-5 mol, of epoxy groups per kg of epoxy-modified silicon dioxide.

Furthermore, both coating agents may contain the epoxy-modified silica in the form of particles having a size in the range from 0.1 nm to 10 μm, preferably in the range from 1 nm to 100 nm, particularly preferably in the range from 5 nm to 100 nm, for example about 10 nm or about 50 nm. The size of the particles is determined according to ISO 22412 by means of dynamic light scattering (specialized analysis methods for multimodal size distributions and zeta potential / electrophoretic mobility distributions).

Examples of suitable epoxy-modified alkoxysilanes are compounds of the formula

R ¹ R ² _n Si (OR) ₃ . _{n is} n is 0.1 or 2, preferably 0 or 1, R ^{1 is} an epoxy-functional group,

R ² is hydrogen or any organic radical, for example Ci _-5 alkyl, aryl (especially phenyl), amino-C ^ alkyl, cyclohexyl, or vinyl, and

RO is Ci _-5- alkoxy, preferably methoxy or ethoxy, more preferably ethoxy.

The epoxy-functional group R ¹ may, for example, be an epoxyalkyl group whose alkyl group may be interrupted by one or more heteroatoms, such as oxygen or nitrogen. The alkyl group may also be substituted with one or more substituents such as hydroxy, amino, carboxy or aryl. The alkyl group can be straight-chain, branched and / or ring-shaped available. Preferred alkyl groups contain 1-20, especially 1-10, carbon atoms outside of the oxirane ring. Most preferably, the alkyl group is interrupted by an oxygen atom. A particularly preferred epoxy-functional group is the glycidoxypropyl group.

Examples of suitable epoxy-modified alkoxysilanes are 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3,4-

Epoxybufyltrimethoxysilane, 3,4-epoxybutyltriethoxysilane, 2- (3,4-

Epoxycyclohexyl) ethyltrimethoxysilane, 3-glycidoxypropyldimethylethoxysilane, 3-glycidoxypropyldimethylmethoxysilane, 3-glycidoxypropylmethyldiethoxysilane and 3-glycidoxypropylmethyldimethoxysilane.

As an additional problem has emerged in the development of known from the prior art coating method that the metal alkoxide used as a curing catalyst tends to precipitate from the coating agents, for example in the form of oxides, in particular aluminum oxide. It has surprisingly been found that this undesired reaction, if it occurs, can be suppressed by the curing catalyst already being present during the condensation of the epoxy-modified alkoxysilane. It is believed that the cure catalyst in this case complexes with the epoxy groups of the epoxy-modified alkoxysilane, whereby the cure catalyst is homogeneously distributed in the resulting epoxy-modified silica sol and does not precipitate in aqueous solution to form a metal oxide.

In addition, it has been found that the curing catalyst, if already present during the condensation of the epoxy-modified alkoxysilane, shifts the reaction equilibrium to the side of the silica without the need, as described in CA 2,560,335 A1, for liberating the alcohol from the reaction solution to move the balance to the side of the silica. The use according to the invention of a metal alkoxide as curing catalyst thus has the additional advantage that the epoxy-modified silica-containing sol can be prepared more simply and more quickly, since the alcohol released can remain in the solution. The corrosion protection effect of the corrosion protection coating obtained by the process according to the invention is carried out by the metal particles contained in the first layer. These provide a cathodic corrosion protection. Suitable metals include, for example, zinc, aluminum, tin, iron, manganese, magnesium, copper, nickel, chromium, molybdenum, and mixtures or alloys thereof. Suitable metal alloy particles are, for example, zinc-aluminum particles, zinc-magnesium particles, zinc-nickel particles and chromium-nickel-iron particles. In particular, zinc and zinc-aluminum alloys provide highly effective cathodic corrosion protection.

The metal particles can be used in the form of powders or so-called flakes, with platelet-shaped flakes assisting the layer formation when the coating composition is applied to a substrate.

The metal particles may be used singly or in any mixture of two or more metal particles.

In addition, it may be advantageous if the first coating agent contains, in addition to the metal particles, organic or inorganic conductive substances such as, for example, iron phosphide, carbon black or nanotubes.

The size of the metal particles used is not particularly limited and may be, for example, in the range of 0.1-50 μm, preferably 1-20 μm. Also, the amount of the metal particles used is not particularly limited. It depends on the metal particles used and the desired corrosion protection effect and can, for example, in the range of 1-90 wt .-%, preferably 20-80 wt .-%, particularly preferably 50-70 wt .-% metal particles based on the dry weight of the first Coating agent are, where dry weight, the weight of the constituents of the coating composition is understood without solvent.

In a further embodiment, the second coating agent contains metal particles. As a result, the temperature resistance of the corrosion protection coating obtained is increased to over 300 ° C, so that the coating is suitable for example for brake discs. As the metal particles, the above-described metal particles may be used in the second coating agent. Preference is given to aluminum particles.

It can be advantageous if, in addition, an emulsifier is added so that the metal particles are distributed easily and homogeneously in the coating composition.

Both coating compositions may additionally contain, independently of one another, additional components such as, for example, crosslinking agents, adhesion promoters, additives, thickeners, fillers, corrosion inhibitors, anticorrosion pigments and also coloring pigments.

In a preferred embodiment, the first and / or the second coating agent contains a black filler which simultaneously acts as a coloring pigment. For example, black iron oxide, spinels, carbon black, graphite and MoS ₂ are suitable for this purpose.

In one embodiment, the coating agent, if it contains a filler, does not contain aluminum particles. Preferably, a combination of black iron oxide pigment and zinc particles is used. Particularly preferably, this combination is present in the first coating agent.

In a further embodiment, the first and second coating agents contain a black pigment, for example iron oxide.

If the second coating agent contains a pigment, in particular a black pigment, such as, for example, iron oxide, it is possible to dispense with the metal particles in the second coating agent. In this case, the second coating agent is preferably free of metal particles.

Since the coating compositions should be liquid during their application, they also have a solvent. Suitable solvents are, for example, water and alcohols, in particular methanol and ethanol, more preferably ethanol. In a preferred embodiment of the present invention, both coating agents are aqueous. For example, the coating agents may contain the alcohol liberated in the preparation of the epoxy-modified silica, but it is desirable to minimize the amount of alcohol in the coating agent since the alcohol is released upon final cure. Accordingly, it is advantageous if at least the second, but preferably both, coating compositions contain less than 10% by weight, preferably less than 5% by weight and particularly preferably less than 3% by weight of alcohol, based on the total weight of the particular coating composition.

The first layer may be partially cured prior to application of the second layer. However, the method according to the invention is particularly advantageous if the second layer is applied to the first layer which has not yet been cured, wherein "not cured" here includes drying of the first layer. In this context, "drying" or "drying" is understood to mean a process in which essentially only, preferably exclusively, solvent used evaporates, without any crosslinking of the binder molecules taking place. The actual curing then takes place by the chemical crosslinking reaction of the binder molecules, with partial curing meaning partial crosslinking. Since the crosslinking reaction takes place only at higher temperatures and over time, the drying, drying, partial curing and complete curing of the first layer can be adjusted by selecting suitable temperatures and holding times.

The drying or drying of the first layer can be carried out, for example, at room temperature (about 23 ° C.) for 10 seconds to 60 minutes, preferably for 1 to 20 minutes. At higher temperatures, the time should be shorter, with the temperature usually not exceeding 100 ° C, preferably 85 ° C, more preferably 50 ° C, so as not to favor crosslinking of the binder molecules. For example, the drying of the first layer at a temperature in the range to less than 85 ° C, preferably up to 80 ° C, to 50 ° C to 45 ° C, to 40 ° C, to 38 ° C, to 35 ° C, to 33 ° C or up to 30 ° C. A temperature range from 20 to 40 ° C., in particular from 30 to 40 ° C., for a period of from 5 seconds to 1 minute, preferably from 5 seconds to 30 seconds, particularly preferably from 5 seconds to 15 seconds, is preferred. Depending on the binder selected However, the temperature may also be higher, without a crosslinking reaction of the binder molecules used, for example, 80 ° C to 100 ° C for 6 sec. To 10 sec. Thus, in a particularly preferred embodiment of the process according to the invention, the first layer is wet-chemically applied to a substrate which is for example slightly preheated to about 50 ° C., preferably about 40 ° C., and at about 80 ° C. to about 100 ° C. for about 6 seconds to about 10 sec. Dried without crosslinking the binder. The second layer is then wet-chemically applied to the first layer. As a result, the first layer dries slightly on the substrate, but due to the relatively low temperature and the short time, curing of the first layer does not occur. On the other hand, the drying of the first layer before the application of the second layer prevents unwanted mixing of the constituents of the layers with one another.

The application of the layers can be done by conventional methods such as spraying or dipping.

The applied layers can each have a dry film thickness in the range from 1 to 50 μm, preferably in the range from 5 to 30 μm. In particular, low layer thicknesses lead to improved flexibility of the coating, so that, for example, coatings on spring materials are less likely to chip off.

In the method according to the invention, the two layers are finally cured simultaneously. The curing is carried out by heating, for example, to a temperature in the range of 50-300 ° C. The inventive method is characterized in an advantageous manner, however, characterized in that due to the curing catalyst used curing at a relatively low temperature in the range of, for example, 80 ° C to 200 ° C, preferably 80 ° C to 150 ° C, in particular about 1 10th ° C can take place.

In the method according to the invention, the anticorrosion coating can be applied to any suitable substrate and in particular to any metallic substrate. Examples of suitable substrates are engine blocks, rims, gearbox housings, bodies and their parts, brake discs, attachments, axles, carrier parts, fasteners, crossbeams, control arms, gears, pipes, pipelines, masts, crash barriers, railings, scaffolding, sheets, screws, bolts, Rivets and profiles. In a preferred embodiment, the anticorrosive coating according to the invention is applied to brake discs. Advantageously, the brake disk is first heated slightly, for example, to a temperature of about 40 ° C, and the first coating agent is applied to the heated brake disk. As a result, the first layer dries immediately, but does not harden. The second layer is then applied to the dried but not cured first layer and both layers are subsequently cured simultaneously. Curing can be carried out at a relatively low temperature in the range of, for example, 100 ° C to 200 ° C, preferably in the range of 100 ° C to 150 ° C, such as about 110 ° C or 130 ° C, due to the curing catalysts employed in the two coating compositions C done.

The drying but not curing of the first layer after its application to the preheated substrate, in particular the brake disc, has the advantage that little energy is consumed and also the corrosion protection coating can be produced at high speed, since a separate, even only partial curing of the first Layer is not necessary.

Finally, the present invention relates to the corrosion protection coating obtainable by the process according to the invention.

The attached Figure 1 shows the attack of the lower layer of a non-inventive corrosion protection coating by rim cleaner.

The appended FIG. 2 shows the resistance of a corrosion protection coating according to the invention to rim cleaners.

The invention will now be explained in more detail with reference to the following examples, without these being intended to be restrictive. Examples

Example 1: Binder

Example 1.1:

To 100 g of 3-glycidyloxypropyltriethoxysilane 10 g Aluminiumbutoxyethanolat be added rapidly under a nitrogen atmosphere with stirring, so that a clear solution is formed. The solution is cooled down to 4 ° C, with vigorous stirring, 50 g of silica sol Levasil 200S / 30% Bayer Bayer are added dropwise within about 30 min and stirred vigorously for about 5 h. The result is a slightly cloudy low-viscosity solution.

Example 1.2:

30 g of an organic complex-stabilized aluminum complex dissolved in 2-butanol (x-add® KR 9006, NANO-X) are added to 100 g of 3-glycidyloxypropyltriethoxysilane and the mixture is stirred for about 5 minutes to give a water-clear colorless solution. 100 g of silica sol Ludox TMA (from Grace) are added to the batch and stirred vigorously for about 5 hours.

Example 1.3:

To 100 g of 3-glycidyloxypropyltriethoxysilane, 20 g of an organic complex-stabilized aluminum complex dissolved in 2-butanol (x-add® KR 9006, NANO-X) are added rapidly and stirred for about 5 minutes, so that a water-clear solution is formed. 400 g of silica sol Klebosol 30 ca! 25 and stirred vigorously for about 5 h. The result is a whitish low-viscosity solution.

Example 2: first coating agent

Example 2.1:

500 g of the binder prepared according to Example 1.3 are placed in a beaker and mixed with 25 g of a fumed silica (eg Cab-O-Sil® EH5, Cabot) and dispersed for 2 h with a dissolver. To the approach 250 g of platelet-shaped zinc flakes having a diameter of 0-20 pm and 25 g of platelet-shaped aluminum pigment having a particle diameter of 10-20 pm and 200 ml of distilled water and 3 g of emulsifier (Marlipal® 24/60, from Sasol) are added and with a Propeller stirrer stirred for 4 h and stirred for a further 12 h.

Example 2.2:

500 g of the binder prepared according to Example 1.2 are placed in a beaker and admixed with 25 g of a fumed silica (for example Aerosil® 300, Evonik) and dispersed in for 2 hours with a dissolver. 250 g of platelet-shaped zinc flakes having a diameter of 10-20 μm and 100 g of black iron oxide pigment and 200 ml of distilled water and 3 g of emulsifier (Marlipal® 24/60, from Sasol) are added to the batch and stirred in with a propeller stirrer for 4 h and stirred for another 12 h.

Comparative Example 1: Corrosion Protection Coating (Not According to the Invention)

To 50 g of glycidyloxypropyl methoxysilane (Dynasylan Glymo, Degussa) are added according to CA 2,560,335 A1 127.3 g of Levasil 200E (Bayer) and stirred for 3h. The solids content of the sol is about 35% by weight.

This second coating composition is overcoated (topcoat) with zinc and aluminum-pigmented anticorrosion paint according to Example 2.1, baked together at 110 ° C. Layer thickness base coat approx. 15 pm, topcoat approx. 10 pm.

After 10 min exposure to rim cleaner "AII minium devil", pH 0.8 (to the left of the black line in Figure 1, to the right of the line NaOH 5%) clear attack of the lower layer visible.

Example 3 Corrosion Protection Coating (According to the Invention)

To 50 g of Dynasylan Glymo (Degussa) are added 5 g of x-add KR 9006 and, after homogeneous mixing, 127.3 g of Levasil 200E (Bayer) and stirred for 3 h. The solids content of the sol is about 35% by weight. This second coating agent as an overcoat (topcoat) for zinc and aluminum pigmented anticorrosive paint according to Example 2.1, baked together at 1 10 ° C. Layer thickness base coat approx. 15 μιη, topcoat approx. 10 μιη.

After 10 min exposure of rim cleaner "aluminum devil", pH 0.8 (to the left of the black line in Figure 2, to the right of the line NaOH 5%) no attack of the lower layer visible.

Example 4: alternative second coating agent

To 50 g of glycidyloxypropyltriethoxysilane (Dynasylan Glyeo, Degussa) are added 5 g of x-add KR 9006 (NANO-X) and, after homogeneous mixing, 200 g of Klebosol 30cal 50 (AZ Electronic Materials) and stirred for 5 h. Thereafter, 10 g of aluminum pigment Stapa 777n.l. and 1 g of Byk 348 added and the aluminum pigment stirred for about 5h homogeneous.

Claims

claims

1 . Method for producing a corrosion protection coating on a substrate, comprising the steps:

c) simultaneously curing the first and second layers;

characterized in that a metal alkoxide is used as the curing catalyst in the first and second coating agents, wherein the metal alkoxide is not silicon alkoxide.

2. The method of claim 1, wherein the curing catalyst is selected from the group consisting of alkoxides of aluminum, titanium, zirconium, tantalum, niobium, tin, zinc and tungsten.

3. The method of claim 2, wherein the curing catalyst is selected from the group consisting of zirconium iso-propylate, zirconium n-propylate, zirconium tert-butoxide, tantalum ethanolate, tantalum tert-butoxide, niobium ethoxide, niobium tert. butylate, tin tert-butylate, tungsten (VI) ethanolate, germanium ethanolate, germanium iso-propylate, titanium (IV) methoxide, titanium (IV) ethoxide, titanium (IV) sec-butoxide, titanium (IV) Tertiary butylate, titanium (IV) isobutylate, titanium (IV) isopropylate, titanium (IV) n-propylate, titanium (IV) 2-ethylhexyl oxide, titanium (IV) - (triethanolaminato) isopropoxide, ^' titanium diisopropoxide bis (acetylacetonate), dibutyltriethanolamine titanate, tetraphenyltitanate, tetrahexyl titanate, titanium (IV) -2-propenolate, tetrakis (ethylpropyl) titanate, tetrapentyl titanate, tetrakis (1,1-dimethylpropyl) titanate, tetrakis (3-methylbutyl) titanates, Tetrakis (1, 1-dimethylbutyl) titanates, tetrakis (1-methyl-1-ethylpropyl) titanates, aluminum methoxide, aluminum ethylate, aluminum n-propylate, aluminum isopropylate, Al uminium n-butoxide, aluminum sec-butoxide, aluminum tert-butylate, aluminum isobutylate, aluminum butoxide ethoxide, zirconium ethoxide, tetra-n-butyl butylzirconate, tetra-sec-butylzirconate, tetra-tert-butylzirconate, zirconium tetrakis (1,1-dimethyl-propoxide) and tetrapentylzirconate.

4. The method according to any one of the preceding claims, wherein the curing catalyst is used in complexed form.

A process according to any one of the preceding claims, wherein the first and second coating agents contain the same epoxy-modified silica and curing catalyst.

6. The method according to any one of the preceding claims, wherein the curing catalyst is present in both coating compositions each in an amount of 0.5 to 20 wt .-% based on the weight of epoxy-modified silica in the respective coating agent.

A process according to any one of the preceding claims, wherein the epoxy-containing silica has been obtained by condensation of epoxy-modified alkoxysilane.

8. The method according to any one of the preceding claims, wherein the epoxy-modified silica in both coating agents each 0.5-10 mol, preferably 1-5 moles of epoxy groups per kg of epoxy-modified silica.

9. The method according to any one of the preceding claims, wherein in both coating agents, the epoxy-modified silica in the form of particles of a size in the range of 0.1 nm to 10 pm, preferably in the range of 1 nm to 100 nm.

10. The method according to any one of claims 7-9, wherein the epoxy-modified alkoxysilane has the general formula:

wherein n is 0.1 or 2, preferably 0 or 1, R ^{1 is} an epoxy-functional group, R ² is hydrogen or any organic radical, for example C _ ₅ alkyl, aryl, amino-C _-5 alkyl, cyclohexyl, or vinyl, and

RO is C _{1 -5-} alkoxy.

1 1. The process of claim 10 wherein the epoxy modified alkoxysilane is selected from the group consisting of 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3,4-epoxybutyltrimethoxysilane, 3,4-epoxybutyltriethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3 Glycidoxypropyldimethylethoxysilane, 3-glycidoxypropyldimethylmethoxysilane, 3-glycidoxypropylmethyldiethoxysilane and 3-glycidoxypropylmethyldimethoxysilane.

12. The method according to any one of claims 7-1 1, wherein the curing catalyst is already present during the condensation of the epoxy-modified alkoxysilane.

13. The method according to any one of the preceding claims, wherein the second coating agent contains metal particles.

14. A process according to any one of the preceding claims wherein the metal particles are selected from the group consisting of zinc, aluminum, tin, iron, manganese, magnesium, copper, nickel, chromium, molybdenum and mixtures or alloys thereof.

15. The method according to any one of the preceding claims, wherein the metal particles have a size in the range of 0, 1-50 pm, preferably 1-20 pm.

16. The method according to any one of the preceding claims, wherein the first coating agent 1 to 90 wt .-%, preferably 20-80 wt .-% metal particles based on the dry weight of the first coating composition.

17. The method according to any one of the preceding claims, wherein the first and / or the second coating agent contains a coloring pigment, in particular a black pigment.

A process according to any one of the preceding claims wherein the first and / or second coating agent contains less than 10% by weight, preferably less than 5% by weight of alcohol based on the total weight of the particular coating agent.

A method according to any preceding claim, wherein the second layer is applied to the uncured first layer.

20. Anti-corrosion coating on a substrate, obtainable by a process according to one of claims 1 -19.