Method for the production of weather-resistant powder...

Coating processes – Direct application of electrical – magnetic – wave – or... – Polymerization of coating utilizing direct application of...

Reexamination Certificate

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C427S195000, C427S508000, C427S557000, C427S559000, C427S595000

Reexamination Certificate

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06537620

ABSTRACT:

BACKGROUND OF THE INVENTION
The invention provides a process for preparing exterior weather-resistant powder coatings on metallic and non-metallic substrates.
The decorative or functional coating of surfaces with powder coatings has found a wide range of applications when coating metals due to the high economic viability of the process and the favourable assessment from the point of view of protecting the environment. Numerous powder coating formulations have been developed for different areas of use. For coatings which are subject to UV irradiation, for example those exposed to outdoor conditions (architectural paint, window profiles, garage doors, metal doors, garden furniture, car parts, etc.), stable powder coating systems, for example based on polyester resins with terminal carboxyl groups, have been developed. The polyester resins are generally cured with low molecular weight, high-functional cross-linking agents such as polyfunctional epoxides or hydroxyalkylamides.
Exterior weather-resistant powder coatings based on polyesters which are based on aromatic carboxylic acids such as terephthalic acid or isophthalic acid have been known and used for some time. Powder coatings which are based on these polyester resins are cost-effective to prepare and the coatings have good mechanical properties and a resistance to weathering which is adequate for many applications, in particular in regions with moderate climatic conditions. These types of powder coating systems are cured on the substrate using known, conventional, methods.
There has been no lack of attempts to increase the weather-resistance of powder coating systems. For example, attempts have been made to improve the weather-resistance of powder coatings by the use of polyester resins which are built up exclusively or mainly from aliphatic and/or cycloaliphatic components. These polyester resins are described, for example, in U.S. Pat. No. 5,486,988 and in EP 0 561 102. Although powder coatings prepared from these resins show improved weather-resistance, they have substantially poorer mechanical properties and much higher raw materials costs than the systems based on aromatic carboxylic acids mentioned above.
Therefore, there is the object of providing cost-effective powder coating coatings which do not have the disadvantages described above. In particular, the powder coatings should satisfy demands for increased weather-resistance so that they can also be used, for example, in regions with extreme climatic conditions without deterioration of the coatings.
SUMMARY OF THE INVENTION
This object can be achieved by a process in which powder coating coatings based on polyester resins which contain aromatic dicarboxylic acids, their anhydrides and/or esters as essential constituents, and which are cross-linked with low molecular weight, polyfunctional epoxide resins, are cured by the use of radiation in the near infra-red region (NIR).
DETAILED DESCRIPTION OF THE INVENTION
The powder coating compositions may contain, for example, 40 to 95 wt. % of polyester and 1 to 20 wt. % of the low molecular weight, polyfunctional epoxide resins, wherein other conventional constituents may also be present in conventional amounts, so that the amounts of all the constituents add up to 100 wt. %.
The polyesters have a number average molecular weight Mn of, for example, 500 to 10000 and a glass transition temperature of, for example, 30 to 80° C.
The polyesters may contain hydroxyl and/or carboxyl functions, wherein if this type of functionalisation is present the OH value may be, for example, 10 to 200 and the acid value may be, for example, 10 to 200.
The NIR radiation used according to the invention is short-wave infra-red radiation with an intensity maximum in the wavelength range from about 760 to about 1500 nanometres, preferably 780 to 1200 nanometres. The use of NIR radiation to dry lacquers is generally known (Kai Bär, JOT 2/98). According to this method, powder coatings may be cured in a short time with the aid of NIR radiation of high intensity without any substantial warming of the substrate taking place.
Surprisingly, it was found that powder coatings based on polyester resins which contain aromatic dicarboxylic acids such as terephthalic acid or isophthalic acid, their anhydrides and/or esters as essential structural blocks, together with low molecular weight, polyfunctional epoxides as cross-linking agents, when cured with NIR radiation, have a weather-resistance which is much greater than the resistance usually produced with such resin systems which have been cured in a conventional process, for example in a circulating air oven. The mechanical properties such as e.g. the flexibility of the coating, are of at least the same quality as are produced by conventional curing. In addition, NIR curing enables a substantial shortening of the curing time as compared with conventional oven curing.
Powder coating formulations which can be used in the process according to the invention have, as the basis of the binder, hydroxyl and or carboxyl-functional polyesters which contain, as the only or main constituent of the acid structural blocks, aromatic dicarboxylic acids, their anhydrides and/or esters such as, for example, terephthalic acid or isophthalic acid, which are reacted with conventional aliphatic diols such as, for example, neopentyl glycol, ethylene glycol, butylene glycol, hexanediol or diethylene glycol or cyclohexanedimethanol. Examples of other aromatic dicarboxylic acids are naphthaline-2-6-dicarboxylic acid, naphthaline-1,5-dicarboxylic acid and phthalic acid. Carboxyl-functional polyesters based on terephthalic acid and isophthalic acid or their anhydrides are preferably used.
An acid constituent with more than 50% of aromatic dicarboxylic acids, with respect to the dicarboxylic acid fraction in the polyester is preferred, particularly preferably an acid constituent with more than 50 wt. % of terephthalic acid and/or isophthalic acid or their anhydrides and/or esters.
Aliphatic and/or cycloaliphatic dicarboxylic acids such as, for example, adipic acid or cyclohexanedicarboxylic acid are optionally used as minor constituents, wherein the proportion of aliphatic and/or cycloaliphatic dicarboxylic acids is not more than 50%, with respect to the dicarboxylic acid fraction in the polyester. As other components, the polyester resins may contain small amounts of polyfunctional branching agents such as, for example, glycerol or trimethylolpropane and additives such as, for example, accelerators. It is also possible to use mixtures of different polyesters. Polyesters which may be used according to the invention may be prepared conventionally by reacting the dicarboxylic acids, their anhydrides and/or esters with the diols; see, for example, D. A. Bates, “The Science of Powder Coatings”, vol. 1 and 2, Gardiner House, London, 1990.
Powder coating formulations which are suitable for use in the process according to the invention contain the amount of low molecular weight, polyfunctional epoxides, as a cross-linking component, required for curing. The amount is generally 1 to 20 wt. %, with respect to the polyester/epoxide system. Triglycidyl isocyanurate (TGIC), polyglycidyl esters based on terephthalic acid/trimellitic acid (obtainable e.g. from Ciba Spezialitäten Chemie under the tradename Araldite® PT 910), polyfunctional aliphatic oxirane compounds such as are provided, for example, by the company DSM Resins under the tradename Uranox®, or glycidyl-functionalised (meth)acrylate copolymers, for example, can be used as cross-linking agents.
The powder coating formulations, containing polyester and epoxide cross-linking agent, may optionally contain other conventional constituents such as, for example, pigments and/or fillers and optionally other conventional additives such as flow control agents, degassing agents and/or accelerators. These are added in amounts which are familiar to a person skilled in the art. For example, 0 to 50 wt. % of pigments and/or fillers and 0.02 to 3 wt. % of conventional additives are used.
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