MXPA99010766A - Coating powder for the electrostatic coating of glass and ceramic or metallic substrates, the production and use thereof - Google Patents
Coating powder for the electrostatic coating of glass and ceramic or metallic substrates, the production and use thereofInfo
- Publication number
- MXPA99010766A MXPA99010766A MXPA/A/1999/010766A MX9910766A MXPA99010766A MX PA99010766 A MXPA99010766 A MX PA99010766A MX 9910766 A MX9910766 A MX 9910766A MX PA99010766 A MXPA99010766 A MX PA99010766A
- Authority
- MX
- Mexico
- Prior art keywords
- coating
- coating powder
- glass
- powder according
- carboxylic acid
- Prior art date
Links
- 239000000843 powder Substances 0.000 title claims abstract description 94
- 239000011248 coating agent Substances 0.000 title claims abstract description 75
- 238000000576 coating method Methods 0.000 title claims abstract description 75
- 239000011521 glass Substances 0.000 title claims abstract description 47
- 239000000758 substrate Substances 0.000 title claims abstract description 37
- 239000000919 ceramic Substances 0.000 title claims abstract description 19
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 238000009503 electrostatic coating Methods 0.000 title abstract description 8
- 150000003839 salts Chemical class 0.000 claims abstract description 20
- 239000011780 sodium chloride Substances 0.000 claims abstract description 20
- 229910052751 metal Inorganic materials 0.000 claims abstract description 13
- 239000002184 metal Substances 0.000 claims abstract description 13
- 125000004432 carbon atoms Chemical group C* 0.000 claims abstract description 3
- 239000000853 adhesive Substances 0.000 claims description 25
- 230000001070 adhesive Effects 0.000 claims description 25
- 150000001734 carboxylic acid salts Chemical class 0.000 claims description 19
- 239000000463 material Substances 0.000 claims description 16
- 238000010411 cooking Methods 0.000 claims description 9
- 239000008187 granular material Substances 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 8
- 229920001296 polysiloxane Polymers 0.000 claims description 7
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 6
- 238000009826 distribution Methods 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 229910052783 alkali metal Inorganic materials 0.000 claims description 3
- 150000001340 alkali metals Chemical class 0.000 claims description 3
- 238000007590 electrostatic spraying Methods 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 238000001035 drying Methods 0.000 claims description 2
- 238000002156 mixing Methods 0.000 claims description 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract description 4
- 239000002253 acid Substances 0.000 abstract description 2
- 150000001447 alkali salts Chemical class 0.000 abstract 1
- 238000010422 painting Methods 0.000 abstract 1
- UEGPKNKPLBYCNK-UHFFFAOYSA-L Magnesium acetate Chemical compound [Mg+2].CC([O-])=O.CC([O-])=O UEGPKNKPLBYCNK-UHFFFAOYSA-L 0.000 description 10
- -1 polysiloxane Polymers 0.000 description 10
- 238000005034 decoration Methods 0.000 description 9
- 239000011654 magnesium acetate Substances 0.000 description 9
- 235000011285 magnesium acetate Nutrition 0.000 description 9
- 229940069446 magnesium acetate Drugs 0.000 description 9
- 239000000126 substance Substances 0.000 description 7
- 238000002844 melting Methods 0.000 description 6
- 238000001228 spectrum Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 239000004698 Polyethylene (PE) Substances 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 229920000573 polyethylene Polymers 0.000 description 4
- 229910052573 porcelain Inorganic materials 0.000 description 4
- MCMNRKCIXSYSNV-UHFFFAOYSA-N ZrO2 Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 239000003605 opacifier Substances 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-N propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 3
- 229920001169 thermoplastic Polymers 0.000 description 3
- 239000004416 thermosoftening plastic Substances 0.000 description 3
- 239000000037 vitreous enamel Substances 0.000 description 3
- 210000003298 Dental Enamel Anatomy 0.000 description 2
- 229920001353 Dextrin Polymers 0.000 description 2
- 239000004375 Dextrin Substances 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L MgCl2 Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium monoxide Chemical compound [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 235000019425 dextrin Nutrition 0.000 description 2
- 238000004534 enameling Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 206010003402 Arthropod sting Diseases 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 229920001875 Ebonite Polymers 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 238000005524 ceramic coating Methods 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 230000001419 dependent Effects 0.000 description 1
- YIXQSYHBXUBLPM-UHFFFAOYSA-N dioxido(oxo)silane;zirconium(4+) Chemical compound [Zr+4].[O-][Si]([O-])=O.[O-][Si]([O-])=O YIXQSYHBXUBLPM-UHFFFAOYSA-N 0.000 description 1
- 239000004815 dispersion polymerization Substances 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000000834 fixative Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000005243 fluidization Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000007496 glass forming Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- CSNNHWWHGAXBCP-UHFFFAOYSA-L magnesium sulphate Substances [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 230000000737 periodic Effects 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000011505 plaster Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001843 polymethylhydrosiloxane Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 230000001681 protective Effects 0.000 description 1
- 230000001698 pyrogenic Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 150000004819 silanols Chemical class 0.000 description 1
- 238000005245 sintering Methods 0.000 description 1
- 229910052596 spinel Inorganic materials 0.000 description 1
- 239000011029 spinel Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-M stearate Chemical compound CCCCCCCCCCCCCCCCCC([O-])=O QIQXTHQIDYTFRH-UHFFFAOYSA-M 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
Abstract
The invention relates to coating powders for the electrostatic coating of glass and ceramic or metallic substrates. According to the invention, the required high-specific electric volume resistance to electrostatically coat glass and ceramic or metallic substrates is achieved in the presence of a carboxylic by acid salt in a volume of 0.01 to 1 wt%. The coating powders preferably contain alkali salts, alkaline-earth salts or earth metal salts of carboxylic acids with 2 to 6 C-atoms. The resistance can be increased by 3 to 5 powers of ten. The inventive coating powders are used for glazing, slip painting and decorating glass and ceramic substrates as well as for enamelling metallic substrates.
Description
COATING POWDER FOR ELECTROSTATIC COATING
GLASS AS WELL AS CERAMIC AND METALLIC SUBSTRATES, ITS PRODUCTION AND UTILIZATION
DESCRIPTION
The invention relates to a coating powder for electrostatically coating glass as well as ceramic and metal substrates; The main component of the coating powder is a powdery material, which forms a glass layer when cooked. A further object of the invention relates to a process for the production of the coating powder. Another object of the invention is the use of coating powder for glazing, plastering and decorating glass and ceramic substrates, as well as for enameling metal substrates. For the production of ceramic coatings, such as glaze, enamel and vitreous enamel on susceptible substrates, meaning glass and ceramic and metallic substrates, aqueous slips are mainly used. After the application of the slip, the substrate coated with it is fired, melting or sintering the material capable of cooking contained in the slip REF .: 31930
to a vitreous layer, also often called a ceramic layer. Due to the disadvantages linked to the use of aqueous slips, such as drainage problems and a greater demand for energy, electrostatic powder coating is gaining relevance. It is known that coating powders that form a vitreous layer when baked, are sprayed electrostatically on glass as well as ceramic and metal surfaces. Coating powders that can be applied electrostatically must have a sufficiently high specific electrical resistance, usually from 109 to 1014 ohm * m. To achieve the necessary strength, the coating powders are coated with insulating substances, for example, silanols and organopolysiloxanes, isocyanates and carbodiimides. According to the European Patent EP-A 0 382 003, by means of a treatment of ceramic powders with polymethylhydrosiloxanes, in addition to the necessary strength, the adhesion capacity of the powder on the ceramic surface can be simultaneously improved. It is disadvantageous that the process for the production of ceramic powders treated in this way is very expensive. WO 94/26679 instructs on a
improvement of the adhesive strength and clamping of an electrostatically applied glass powder: the coating powder, in addition to a glass powder, contains adhesives that cook without leaving residues, such as polyolefins or dextrins, which are activated during firing thermally, or, by means of humidity, to fix the particles of the layer with each other and with the substrate. Preferred coating powders contain glass frits coated with polysiloxane, in admixture with 10 to 15% by weight of thermoplastic or 5 to 101 by weight of dextrin. Only under specially optimized conditions, which, however, lead to a high cost, it is possible to obtain glazes that can be used in double-walled porcelain fragments. Under conditions already slightly modified, depending on the substrate, glass defects, considerable and disturbances occur partially before reaching the necessary layer thickness. WO 97/08115 teaches on an improvement of the aforementioned problems: when using a glazing or coating composition with a certain granule distribution, namely a value ds;. from 5 to 25 μm, a d9o value less than 35 μm and a diA value equal to or greater than 2 μm, in a coating powder additionally containing an adhesive, is
possible to simplify the production process without having to lose quality in the glaze. In WO 97/08115 it is also shown that in the presence of an organopolysiloxane, the electrical resistance -specific of the coating powder is increased in a desired manner with an increasing amount of adhesive. Above a certain amount of adhesive, however, retro-threading effects occur, so that the necessary layer thickness can no longer be applied, and thus, the cooked layer is too thin and, therefore, has defects. A problem of the electrostatic coating of glass and ceramic substrates is also that the coating powders, depending on their composition and their granule spectrum, have a very different specific resistance of passage. In addition, the coated substrates have a very diverse surface conductivity and are additionally dependent on the climatic conditions in the coating chamber. A perfect electrostatic coating presupposes that the specific flow resistance of the coating powder is adjusted to the substrate to be coated and to the climatic conditions. Whereas, up to now, a specific resistance of the coating powder as high as possible has always been demanded, meanwhile it has been demonstrated
that too high resistances, although in the case of reduced layer thicknesses, such as the usual thicknesses of 10 to 80 μm for glass decorations, are suitable, in the case of higher layer thicknesses, such as 100 to 400 μm , as required for tile glazes, if you have too high a resistance, retro-threading effects occur. Therefore, the object of the present invention is to provide a new way of simply adjusting the specific step resistance of a coating powder, so that it can be applied electrostatically without problems and that produces perfect baked coatings. It has been observed that the salts of the carboxylic acids can be used as effective auxiliaries to increase the specific step resistance of the coating powders. From the time of adding very small amounts of a carboxylic acid salt, for example, 0.05% by weight of magnesium acetate, it is possible to raise the specific step resistance of a glass powder by up to 2 to 3 powers of ten. Thus, the object of the invention is a coating powder for electrostatically coating glass as well as ceramic and metal substrates, which
includes a pulverulent material that when baking forms a glass bale, characterized in that it contains a salt of a carboxylic acid in an amount of 0.01 to 1% by weight. The carboxylic acid salts are based on an aliphatic or aromatic carboxylic acid with one or more carboxyl groups and, optionally, additionally other functional groups, such as hydroxyl groups. Preferred are aliphatic carboxylic acids having 1 to 6 carbon atoms and 1 to 2 carboxyl groups, and optionally, 1 or 2 additional functional groups. Particularly suitable are the lower aliphatic monocarboxylic acids, especially acetic acid and propionic acid. The cation assortment of the carboxylic acid salt includes metals of the main and secondary groups of the Periodic Table. Preferably, it is an alkali metal, alkaline earth metal or earth metal cation, particularly preferably Li +, NaX K +, Mg: 'X Ca + and Al3X Since a very small amount of carboxylic acid salt is increased. the resistance of the coating powder. Although an amount of less than 0.01% by weight already has an effect, in practice the amount used will be around, and especially over,
0. 01% by weight Conveniently, the amount used is in the range of 0.01 to 1% by weight.An utilized amount of more than 1% by weight, although possible, no longer increases the specific electrical resistance. they employ 0.05 to 0.5% by weight of carboxylic acid salt, especially an alkali metal, alkaline earth or earth metal acetate or propionate.For an optimum resistance increase, the carboxylic acid salt must be homogeneously distributed in the powder. Such a distribution can be easily achieved by intensive dry mixing, especially by using an intensive mixer Alternatively, the powdery material forming the glass layer can be contacted with an aqueous solution or suspension of a salt of carboxylic acid, for example, in the framework of a grinding process, after which the wet product is dried and, if necessary, further separated. It was completely surprising that the salts of carboxylic acids are able to significantly increase, namely by several powers of ten, generally 3 to 5 powers of ten, the specific electrical resistance of the coating powders. In this way resistors are obtained, such as those
they require for the electrostatic application. Whereas, for example, untreated glass powders usually have a specific electrical resistance in the range of 106 to 107 ohm 'm, by adding 0.1 to 0.3% by weight of an acetate, resistances are achieved in the range of 1010 to 1012 ohm 'm. Thus, a treatment with organopolysiloxanes is no longer necessary to increase the strength, but it is not excluded if a resistance is required above that which can be obtained with the carboxylic acid salt. By the presence of a carboxylic acid salt in the coating powder, the electrical charges of the powder particles are better maintained, so that, in the electrostatic spraying, they are better oriented in the electric field towards the workpiece. work connected to earth. In this way, not only the powder can be applied electrostatically, but also, the adhesion of the powder to the substrate is increased, so that the substrates coated in this way can be baked directly. To obtain coatings with an even greater adhesion and clamping force, it may be advisable to make additional use of the technical instruction of WO 94/26679 and / or WO 97/08115. According to WO 94/26679, the powder of
The coating according to the invention can additionally contain, in effective amounts, a powdery adhesive, which can be activated physically, in particular thermally, namely by melting and hardening, or chemical. In the case of thermally activatable adhesives, these are in particular thermoplastics, such as polyethylene, whose binding action is achieved by melting and subsequent hardening. For the purpose of melting, the substrate to be coated, before and / or after being coated, is heated to a temperature above the melting point of the thermoplastic. Among the chemically activatable adhesives, there are two-component resin systems, such as "epoxy-hardener resin combinations, as well as isocyanate-hardener combinations." The amount of adhesive is generally in the range of 1 to 20% by weight, based on the coating powder, but in particular from 1 to 10% by weight The adhesive is introduced into the coating powder, in a known manner, before, during or after dry addition of the carboxylic acid salt. in this case, it is convenient to mix intensively below the activation temperature of the adhesive, in order to guarantee a homogeneous distribution, and with it, a coating free of defects before and after
after cooking According to WO 97/08115, the adhesion strength can also be improved by using a pulverulent material which, when baked, forms a glass layer, with a specific granule spectrum, in particular, from 5 to 25 μm, less than 35 μm and gave equal / greater than 2 μm. Before or after adding the carboxylic acid salt to the pulverulent material, this, if required, should be ground and / or sieved. As indicated above at the point of the adhesives, it is also here, in many cases, advantageous to heat the substrate to be coated before the electrostatic coating. The temperature and duration depend on the substrate. Preheating is particularly convenient in the case of cooked or second-firing fragments, as well as glass. The material that forms a layer of glass when baked is essentially glaze powder, plaster, vitreous enamel and decoration, as well as enamel powder. It can be essentially uniform material, such as glass frits or mixtures thereof, or mixtures of substances: glazing powders of essentially one or more glass frits and, optionally, additional substances of the group consisting of clay, ollastonite, zirconium silicate and white or colored pigments; vitreous enamel powders
of essentially one or several glass frits or the so-called fusions and pigments; In addition to glass frits, they contain substances from the group consisting of fine-particle ceramic raw materials, ground minerals, glass and porcelain flour, opacifiers and pigments. In the case of mixture of substances, it can be advantageous to use them in the form of so-called spray granules, in order to avoid demixing and achieve a uniform melting behavior. Preferably, the materials forming a glass layer are already in the coating powder at 30 to 100% by weight, in particular more than 50% by weight, in the fritted state. The electrostatically coated substrates are baked directly or after further decoration of the surface, for example, including a fixation of the layer, using a. polymeric fixative, and a decoration, using a decal or by serigraphy. The temperature and duration of the cooking depend on the substrate and the type of coating powder. It can be, for example, a typical decoration cooking or a quick cooking at one time, simultaneously cooking the uncooked substrate and the applied coating. In addition to the additives mentioned above in the
electrostatically applicable coating powders, these may also contain customary fluidizing agents, such as pyrogenic oxides, such as Si02, A1203, Ti02, Zr02, in effective amounts, such as 0.05 to 3% by weight, especially 0.1 to 0.5% by weight, thereby improving the electrostatic spraying of the powder. The coating powder according to the invention can be used for glazing, plastering, enamelling and decorating cooked and uncooked ceramic substrates and glass, as well as for enameling metals. The use includes the electrostatic coating under known conditions and the firing of the substrate. A special use of the coating powders according to the invention refers to the production of glass decorations, especially corrosion imitations or high-gloss color decorations, which are provided with additional decoration, such as an inscription. In the prior art, this type of decorations, for example, imitations of corrosion with additional decoration, were produced using polymer systems, which required two firings. As has also been found, alternatively to the use of the aforementioned systems according to the invention, i.e. the coating powders with a carboxylic acid salt, this type
of decorations can also be obtained by employing other electrostatically applicable coating powders, the specific strength of which is high enough, for example, those containing polysiloxanes. For the production of these decorations, an electrostatically applicable coating powder, especially one with a value dso less than 10 μm and a specific electrical resistance of more than 1010 ohm ', preferably 1012 to 1014 ohm "m, is sprayed electrostatically on a pre-heated glass (100 to 250 ° C), in such an amount that the layer thickness after baking is 10 to 50 μm.The coating can be fixed in a known manner by spraying with a polymer dispersion. applying a decoration in a known manner, for example, by means of silk-screen printing or the decal technique, followed by the cooking, simultaneously cooking the basic decoration, for example, the imitation of corrosion, and the additional decoration. To achieve a corrosion effect, the coating powder contains an opacifier, such as Si02, Zr04, Ti0, Zr02 and spinel, or multi-phase glass systems. If necessary, the coating powder contains a carboxylic acid salt and / or an organopolysiloxane and / or an organic adhesive and / or a fluidizing agent, which
it can act as an opacifier, in respectively effective amounts. Preferably, the d50 value of the powder is located around / below 5 μm and the value d90 below the value of the cooked layer. So far it is not known to explain the action of increased resistance of the salts of carbsxílico acid. Due to the ionic character of the carboxylic acid salts, a reduction in the strength rather than the increase in accordance with the invention was to be expected. Other salts, such as sulfates, phosphates and chlorides, do not show the action according to the invention (see comparative tests). It was also surprising that the salts of short-chain aliphatic carboxylic acids, to which, compared to salts of long-chain carboxylic acids, are not attributed per se hydrophobicizing action, proved to be especially effective. Another advantage of the salts of short-chain aliphatic carboxylic acids consists, moreover, in their easy obtainment, their good solubility in water, and with it, their good distribution capacity in the coating powder. The coating powders according to the invention can be easily produced and the specific electric pitch resistance can be adjusted reliably, depending on the amount of use. Other
advantages are the good adhesion to the substrate, as well as the possibility of renouncing the use of organopolysilanes and / or adhesives or of reducing the amounts of use of these substances. The carboxylic acid salts in the coating powder do not cause any defect in the baked coating. A further advantage of the coating powders according to the invention, which also contain an adhesive with a high specific electrical resistance, consists in that when electrically coating, no demixing due to electrostatic issues occurs which, until now, could produce that the coated substrate contained a greater portion of adhesive than the powder that did not come into contact with the substrate at the time of spraying. It is obvious that demixing is avoided because the specific electrical resistance of the material forming glass is similar to that of the adhesive. Thus, when using the powder according to the invention, a new adjustment of the adhesive content is not necessary. Another advantage of the coating powders according to the invention is that by occupying the active centers of the glass-forming material with a carboxylic acid salt, the flowability is improved. In this way, you can eliminate the addition of
other fluidization agents, and the opacities of a coating baked on glass are avoided. The invention is illustrated in more detail with the aid of the following examples and comparative examples. General specifications: a) Production of coating powders: They are ground for 25 minutes in a mill
Bloch-Rosetti 500 g of glass frit with x% carboxylic acid salt in 200 ml of water. They are dried at 110 ° C, then milled 5 minutes dry and, if indicated, sieved. b) Production of a coating powder containing an adhesive: A frit without salt of carboxylic acid, respectively, a frit with carboxylic acid
(obtained according to part a)), it is mixed intensively with the adhesive, homogenizing the respective raw mixture using an intensive mixing device. Polyethylene wax having a softening temperature of 135 ° C and a granule spectrum of di; of 1.8 μm, ds, -, of 10.5 μm and dg0 of 16.9 μm. c) Determination of the specific electric pass resistance of the coating powder:
Method and measuring device according to DIN IEC 93: - cylindrical measuring cell with protective collar electrode; - distance between electrodes 5 mm; high strength meter type Teralog 6202 (STATRON); - selected measuring voltage UM = 1 V up to a specific resistance of 106 ohm m, 10 V up to 107 ohm 'm; UM = 1000 V in powders with a specific resistance > 109 ohm 'm. The measuring voltage was always applied 1 minute after filling the powder sample in the measuring cell (to guarantee constant and reproducible stacking dust densities in the inter-electrode space). The measurement values are read 1 minute after applying the measurement voltage. d) Electrostatic coating: Double-walled porcelain fragments (15 x 15 cm) were coated, without preheating. High voltage gun with flat jet nozzle; 70 kV with 60 μA. e) Determination of the adhesion strength of the coating powder applied electrostatically: The electrostatically coated fragments
They are placed on the head (coated side down) and fixed in a holder provided for this purpose. From a defined height (h = 70 cm) a hard rubber sphere (m = 0.005 kg) is dropped to the center of the substrate, an electrostatically charged powder remains attached to the ceramic fragments after the drop test. The substrate after said test is checked in relation to the total application of original powder.The adhesion force of the glass powder is obtained in percent.
Example 1 For the production of a glaze coating powder for tiles a glass frit was used "TGF 2486 A from Cerdee AG, which contains as main components Si02, ZnO, B203, A1203, MgO, CaO, KXD and ZGO (sample 1.1) In a manner analogous to general specification a), but in a proportion 150 times greater, a grinding duration of 75 minutes in a ball drum mill and roller drying, the frit was mixed with 0.21 in weight of magnesium acetate (sample 1.2), sample 1.1 corresponds to the frit treated in the same way in the absence of magnesium acetate Sample 1.2 was sieved (sample 1.3).
Table 1 shows the specific electrical resistance as well as the granule spectrum of the samples.
Table 1 Sample No. Electrical resistance Specific granule spectrum (ohm 'm) d10 (μm) d50 (μ) d90 (μm)
1. 1 5 X 108 2.6 24.0 66.5
Tests show that even 0.2% by weight of magnesium acetate increases the resistance in 4 powers of ten. By screening the powder, an additional increase is possible.
EXAMPLE 2 Coating powders 1.1 and 1.2 of Example 1, as well as coating powders 1.1 H and 1.2 H containing polyethylene wax as adhesive, were applied according to the general specification d) electrostatically onto second-grade porcelain fragments, and then the coated fragments were baked. The production of samples 1.1 H and 1.2 H was carried out according to the general specification
b), the amount of adhesive being respectively 6% by weight, based on the coating powder. The adhesion strength was determined in% (average of 5 measurements) according to the 'general e' specification as well as the application amount for 60 seconds (average of 5 measurements), and also, the specific electrical step resistance according to the general specification c), as well as the surface quality of the baked glaze for 60 minutes at 1170 ° C. The results are shown in Table 2.
Table 2 Sample No. Electrical resistance Ad-Qty Strength of Specific Quality (ohm 'm) hesity (%) api. (g / min) glaze 1.1 5 x 108 5.2 2.4 n.d. * lT2 - 5 x 101 81.5 15.5 good **
1. 1H 7 x 10 ?: 82.9 15.0 good **
1. 2H 5 x 10: 84.0 15.1 good **
* n.d. = not determined, as it was not cooked due to insufficient powder application. ** good = smooth and soft surface; no stings, no orange peel effect; without defects (bubbles, points or glazes).
The tests show that an addition of 0.2% by weight of magnesium acetate to a glaze powder increases the adhesion strength in the same way as an addition of 6% by weight of polyethylene wax.
Example 3 A glaze frit (TGF 2486 A from Cerdee AG) was mixed according to the general specification a) with different amounts of magnesium acetate. Sample 3.0 corresponds to the frit treated according to a) in the absence of magnesium acetate; 3.0 granule spectrum: gave 1-2 μm, dso 8.6 μm, d90 34.9 μm. As can be seen in Table 3, the specific electric resistance resistance of the coating powder is considerably increased with an increasing amount of magnesium acetate.
Table 3 Sample No. Magnesium acetate Step resistance (% by weight) elec. spec. (ohm 'm)
3. 0 0 < 107 3.1 0.05 1 x 10-
3. 3 0.25 1 x 10 12
Example 4 Analogously to Example 3, according to the general specification a) se. they applied various salts on the same glass frit respectively (290/498 from the company Cerdee AG), namely respectively in an amount of 0.2% by weight. Table 4 shows the specific electric resistance resistance of the different powders, the powder No. 4.0 not containing any salt and "powders Nos. 4.9 to 4.11 in accordance with the invention." Powders Nos. 4.9 to 4.11 contain other salts that salts of carboxylic acid (not according to the invention), which does not produce any increase in the resistance or only a very small increase.
Table 4 Sample No. Salt Resistance of elec. spec. (ohm 'm)
4. 0 < 10 '4.1 Mg stearate 5 x 1011 4.2 Ca acetate 2 x 1011 4.3 Mg acetate 2 x 1011 4.4 Zn acetate 6 x 1011- 4.5 Na acetate 1 x 10 11 4.6 K acetate 5 x 10 10
4. 7 Al Acetate 4 x 1010 4.8 Acetatohydrate (III) of La 3 x 1011 4.9 MgSO4. 7 H20 < 10 '4.10 MgCl2 < 107 4.11 Mg Phosphate 4 x 108
It is noted that in relation to this date, the best method known to the applicant to carry out the aforementioned invention, is that which is clear from the present description of the invention.
Having described the invention as above, property is claimed as contained in the following:
Claims (9)
1. A coating powder free of organopolysiloxane, for electrostatically coating glass as well as ceramic and metal substrates, which includes a powdery material which, when baked, forms a glass layer, characterized in that it contains a salt of a carboxylic acid in an amount of 0.01 to 1. % in weigh.
2. A coating powder according to claim 1, characterized in that it contains an alkaline, alkaline earth or earth metal salt of a monocarboxylic acid having 2 to 6 carbon atoms.
3. A coating powder according to claim 1 or 2 / characterized in that it contains an alkali metal, alkaline earth or earth metal acetate in an amount of 0.05 to 0.5% by weight.
4. A coating powder according to any of claims 1 to 3, characterized in that it was obtained by a method that includes the contact of an aqueous solution of the carboxylic acid salt with the powdery material forming a glass layer at the cook, and drying.
5. A coating powder according to any of claims 1 to 4, characterized in that it additionally contains a chemically or thermally activatable powdery adhesive in an amount of 1 to 10% by weight.
6. A coating powder according to any of claims 1 to 5, characterized in that the powdery material forming a glass layer has a granule distribution with a dgo value of less than 35 μm, a value dso in the range of 5 to 25 μm and a value gave greater than 1 μm.
7. A coating powder according to any of claims 1 to 6, characterized in that the powdery material forming a glass layer has a composition that forms a glaze or a coating and is present in the form of 30 to 100 * by weight of a glass frit.
8. A process for the production of an organopolysiloxane-free coating powder according to any of claims 1 to 7, characterized in that a pulverulent material which when baked forms a glass layer is contacted wet or dry in a intensive mixing device, with 0.01 to 1 * by weight of carboxylic acid salt and, if the coating powder contains an adhesive, a powdery adhesive is mixed in the dry state to the mixture containing the carboxylic acid salt. .
9. The use of the organopolysiloxane-free coating powder according to any of claims 1 to 7 or obtained according to claim 8, for glazing, plastering and decorating glass and metal substrates, including electrostatic spraying of the coating powder on the substrate and the cooking of the coated substrate.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19722273.0 | 1997-05-28 |
Publications (1)
Publication Number | Publication Date |
---|---|
MXPA99010766A true MXPA99010766A (en) | 2000-09-04 |
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