Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
  • C09D133/04—Homopolymers or copolymers of esters
  • C09D133/06—Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers

Definitions

• the invention relates to a powder coating compostion comprising as a binder a polymer with free carboxylic acid groups and as a crosslinker a compound containing ⁇ -hydroxyalkylamide groups.
• a powder coating comprising a co-reactable mixture of an amorphous carboxylic acid group containing polyester and a ⁇ -hydroxyalkylamide is known from EP-A- 322834.
• the composition described in this application is cured - after application to a substrate - by heating the powder to 160-200°C so that the powder melts, forming a smooth layer. At that temperature the coating is chemically crosslinked due to an esterification reaction between the acid groups of the polymer and the hydroxy groups of the compound containing ⁇ -hydroxyalkylamide groups.
• a de-gasifying agent benzoin (0.5 to 3% by wt. of the powder composition) may be added to the composition.
• a de-gasifying agent is needed to ensure that the air and/or water entrapped due to melting of the powder (during a curing cycle) are removed from the paint layer as a result of the reaction. Any gas bubbles that remain in the coating reduce the adhesion of the coating to the substrate and markedly adversely affect the protection obtainable with the coating.
• compositions are characterized in EP-A-322834 as having good physical properties, such compositions are unsuitable for preparing a white or crystal-clear coating because the powder coating exhibits some degree of browning after curing, as indicated in Mercurio, New Perspective on Hydroxyamide Crosslinkers, 16th International Conf. in Org. Sci. and Tech. 235-49 (Athens, Greece 1990).
• browning appears to intensify upon heating the cured powder coating at a temperature of 200°C for a prolonged period of time (for example between 30 and 60 minutes). This discolouration upon excessive curing (yellowing on overbake) increases with the amount of benzoin. A lower amount of benzoin, on the other hand, results in a lower blister limit, such as lower than 60 ⁇ m, which results in surface defects.
• the object of the invention is to provide a powder coating composition in which it is possible to use a small amount of benzoin, for example between 0.05 and 0.8 wt.%, to obtain the highest possible blister limit, for example higher than 120 ⁇ m.
• the powder coatings must also retain good mechanical properties, such as, for example, good gloss, toughness and impact resistance and chemical properties such as for example a good chemical resistance.
• the invention is characterized in that the crosslinker comprises a combination of at least two compounds containing ⁇ -hydroxyalkylamide groups and each compound having different ⁇ -hydroxylalkylamide functionalities, the first compound having a ⁇ -hydroxy ⁇ alkylamide functionality of . 3 and the second compound having a ⁇ -hydroxyalkylamide functionality of . 3.
• the functionality stands for the average number of ⁇ -hydroxyalkylamide groups per molecule.
• Suitable compounds containing ⁇ - hydroxyalkylamide groups and having a functionality of ⁇ 3 can be depicted structurally according to formula (I):
• R 1 represents hydrogen, an alkyl group with 1- 5 carbon atoms (for example methyl, ethyl, n-propyl, n-butyl, sec. butyl, tert. butyl and pentyl) or a hydroxy- alkyl group with 1-5 carbon atoms (for example 2-hydroxy- ethyl, 3-hydroxypropyl, 2-hydroxypropyl, 4-hydroxybutyl, 3-hydroxybutyl, 2-hydroxy-2-methylpropyl, or the hydroxy derivatives of the pentyl isomers);
• R 2 and R 3 are the same or different and each independently represents hydrogen or a straight or branched alkyl group with 1-5 carbon atoms, while one of the groups R 2 and one of the groups R 3 may also form, together with the adjacent carbon atoms, a cycloalkyl group, such as, for example, cyclopentyl and cyclohexyl; R 2 and R 3 may also be hydroxyalkyl groups, such as, for example, hydroxy (C 1 -C 5 )-alkyl groups, hydroxymethyl and 1-hydroxyethyl, being preferred among the latter and
• A is an alkyl group with (1-10) carbon atoms
• R 1 represents 2-hydroxyethyl or hydrogen
• R 2 and R 3 are independent of one another hydrogen or hydroxy ( Ci-Cj J-alkyl .
• the first compound having a ⁇ - hydroxyalkylamide functionality of ⁇ 3 is a compound according to formula (II):
• Very suitable compounds having a ⁇ -hydroxyalkyl ⁇ amide functionality of ⁇ 3 are compounds according to formula (I) having a ⁇ -hydroxyalkylamide functionality of . 3 or compounds according to formula (III):
• A is an alkyl group with (1-10) carbon atoms
• R 1 represents 2-hydroxyethyl or hydrogen
• R 2 and R 3 are independent of one another hydrogen or hydroxy (C 1 _C 2 )-alkyl.
• the second compound having a ⁇ - hydroxyalkylamide functionality of r. 3 is a compound according to formula (IV):
• the functionality of the second compound having a functionality of ⁇ 3 according to formula (I) is 2.
• Compounds according to formula (V) are also very suitable as compounds having a functionality of _ 3:
• the weight ratio in the crosslinker between is preferably between 90:10 and 10:90 and more preferably between 80:20 and 20:80. This ratio depends on the functionality of the polymer with free carboxylic groups.
• the average functionality of the polymer is between 1.7 and 4.5 and preferably between 2.3 and 3.5.
• the weight ratio of the crosslinker to the polymer is usually between 10:90 and 3:97, more preferably between 20:80 and 3:97.
• the acid number of the polymer containing carboxyl groups is preferably between about 15 and about 150 mg KOH/gram resin, in particular is between about 20 and about 70 mg KOH/gram resin.
• the glass transition temperature, Tg is preferably between about 30°C and about 80°C and in particular ranges between about 35°C and about 65°C.
• the polymer that contains carboxyl groups is a polyester and/or a polyacrylate.
• Examples of preferred monomers for polyacrylates that can be incorporated in the main chain of the polymer are unsaturated monocarboxylic acids, such as, for example, acrylic acid, methacrylic acid and crotonic acid, unsaturated dicarboxylic acids, such as, for example, maleic acid, 2-methyl maleic acid, itaconic acid, and ⁇ - ⁇ -methylene glutaric acid, unsaturated anhydrides, such as, for example, maleic anhydride, itaconic anhydride, acrylic anhydride and methacrylic anhydride.
• unsaturated monocarboxylic acids such as, for example, acrylic acid, methacrylic acid and crotonic acid
• unsaturated dicarboxylic acids such as, for example, maleic acid, 2-methyl maleic acid, itaconic acid, and ⁇ - ⁇ -methylene glutaric acid
• unsaturated anhydrides such as, for example, maleic anhydride, itaconic anhydride, acrylic anhydride and methacrylic anhydr
• the polymer usually also consists of copolymerized esters of (meth)acrylic acid, such as, for example, methyl methacrylate, butyl acrylate, 2-ethyl hexyl acrylate or acrylonitrile, styrene and other ethylenically unsaturated compounds.
• (meth)acrylic acid such as, for example, methyl methacrylate, butyl acrylate, 2-ethyl hexyl acrylate or acrylonitrile, styrene and other ethylenically unsaturated compounds.
• Suitable polyesters can be obtained via standard preparation methods from essentially aromatic poly- carboxylic acids, such as, for example, phthalic acid, isophthalic acid, terephthalic acid, pyromellitic acid, trimellitic acid, 3,6-dichloro phthalic acid, tetrachloro phthalic acid, or, if obtainable, the anhydrides, acid chlorides or lower alkyl esters thereof.
• carboxylic acid component is composed at least of 50% by weight, preferably at least 70 mol %, of isophthalic acid and/or terephthalic acid. Exemplary procedures are described in said reference of Misev at pages 144-162.
• the polycarboxylic acids used can also be cyclo- aliphatic and/or acyclic polycarboxylic acids such as, for example, tetrahydro phthalic acid, hexahydro-endomethylene terephthalic acid, hexachloro tetrahydrophthalic acid, azelaic acid, sebacic acid, decane dicarboxylic acid, dimer fatty acid, adipic acid, succinic acid and maleic acid, in amounts of up to not more than 30 mol%, preferably up to not more than 20 mol%, of the total of carboxylic acids.
• cyclo- aliphatic and/or acyclic polycarboxylic acids such as, for example, tetrahydro phthalic acid, hexahydro-endomethylene terephthalic acid, hexachloro tetrahydrophthalic acid, azelaic acid, sebacic acid, decane dicarboxylic acid,
• Hydroxy-carboxylic acids and/or, optionally, lactones such as, for example, 12-hydroxy- stearic acid, ⁇ -caprolactone and the hydroxypivalic acid ester of neopentyl glycol can also be used.
• monocarboxylic acids such as, for example, benzoic acid, tert-butylbenzoic acid, hexahydro benzoic acid and saturated aliphatic monocarboxylic acids can also be added during the polyester preparation.
• polyols such as
• Suitable compounds for reacting with polycarboxylic acids include monoepoxides such as, for example, ethylene oxide, propylene oxide, monocarboxylic acid glycidyl ester (for example Cardura E10TM; Shell) or phenyl glycidyl ether.
• monoepoxides such as, for example, ethylene oxide, propylene oxide, monocarboxylic acid glycidyl ester (for example Cardura E10TM; Shell) or phenyl glycidyl ether.
• polyesters are prepared, using methods known per se, by esterification or transesterification, optionally in the presence of customary catalysts such as, for example, dibutyl tin oxide or tetrabutyl titanate, a suitable choice of the preparation conditions and of the COOH/OH ratio yielding end products with an acid number between 15 and 150.
• customary catalysts such as, for example, dibutyl tin oxide or tetrabutyl titanate
• the preparation and testing of the powder coating can take place in a customary manner, for example as described in Misev, Powder Coatings; Chemistry and Technology (Wiley and Sons, 1991) pp. 225-226.
• the powder coating can also contain mixtures of polyesters and polyacrylates.
• other resins such as, for example, an epoxy resin, can also be included in the powder coating composition.
• Suitable pigments include, for example, inorganic pigments such as titanium dioxide, zinc sulphide, iron oxide and chromium oxide, and organic pigments such as azo compounds.
• Suitable fillers include, for example, metal oxides, silicates, carbonates and sulphates.
• compositions according to the invention can be used as coating agents for metal, wood and plastic substrates.
• Examples are general-purpose industrial top coats, top coats on machinery and equipment, in particular top coats on metal, for example for tins, domestic and other small equipment, cars and the like.
• the invention will be elucidated with the following, non-restrictive examples and comparative example.
• Example I was repeated, use being made of the listed ingredients in the following amounts by weight (Table I).
• Example 1 The procedure of Example 1 was repeated, to make powder coatings from the ingredients listed in the following table A in the indicated amounts by weight. No acetyl diethanol amine was added.
• Benzoin 2.5 The powder coatings according to Examples I, II and Comparative Example A were electrostatically applied to steel panels and cured, during 15 minutes, at 180°C.
• the blister limit was determined via electromagnetic induction (see the already cited Misev, Powder Coatings, pp. 295-296).
• the powder coating compositions according to the present invention having the specified combinations of ⁇ - hydroxyalkylamides at a constant amount of benzoin yielded coatings having a desirable higher blister limit.
• the coatings obtained using the powder coating compositions according to the present invention also retained the desired mechanical properties.

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• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Wood Science & Technology (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Paints Or Removers (AREA)

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Cited By (14)

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• 1992
  • 1992-07-29 BE BE9200687A patent/BE1006097A3/nl not_active IP Right Cessation
• 1993
  • 1993-07-21 AU AU47631/93A patent/AU664482B2/en not_active Ceased
  • 1993-07-21 WO PCT/NL1993/000155 patent/WO1994003545A1/en not_active Application Discontinuation
  • 1993-07-21 EP EP93918083A patent/EP0652911A1/de not_active Withdrawn
  • 1993-07-27 TW TW82105974A patent/TW248568B/zh active
  • 1993-07-28 CN CN 93116866 patent/CN1086836A/zh active Pending

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