Polyester polyols and their use as the polyol component in two-component polyurethane paints

A polyesterpolyol having hydroxyl numbers of from 100 to 280, acid numbers of from 6 to 28 and stoichiometrically calculated molecular masses of from 750 to 12,000, synthesized from reaction products of

• a) from 8 to 47 mol-% of neopentyl glycol,
• b) from 8 to 42 mol-% of trimethylolpropane,
• c) from 25 to 51 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 1 to 27 mol-% of phthalic acid and/or its anhydride,
• the molar percentages stated under a), b), c) and d) in each case adding up to 100 mol-%.

A polyesterpolyol having hydroxyl numbers of from 110 to 270, acid numbers of from 7 to 26 and stoichiometrically calculated molecular masses of from 750 to 10,00, synthesized from reaction products of

• a) from 10 to 45 mol-% of neopentyl glycol,
• b) from 10 to 40 mol-% of trimethylolpropane,
• c) from 30 to 50 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 1 to 22 mol-% of phthalic acid and/or its anhydride,
• the molar percentages stated under a), b), c) and d) in each case adding up to 100 mol-%.

A polyesterpolyol having hydroxyl numbers of from 120 to 260, acid numbers of from 8 to 25 and stoichiometrically calculated molecular masses of from 780 to 8000, synthesized from reaction products of

• a) from 12 to 43 mol-% of neopentyl glycol,
• b) from 12 to 38 mol-% of trimethylolpropane,
• c) from 32 to 50 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 1 to 17 mol-% of phthalic acid and/or its anhydride,
• the molar percentages stated under a), b), c) and d) in each case adding up to 100 mol-%.

A polyesterpolyol having hydroxyl numbers of from 125 to 255, acid numbers of from 9 to 24 and stoichiometrically calculated molecular masses of from 800 to 7000, synthesized from reaction products of

• a) from 14 to 41 mol-% of neopentyl glycol,
• b) from 14 to 36 mol-% of trimethylolpropane,
• c) from 35 to 49 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 2 to 12 mol-% of phthalic acid and/or its anhydride,
• the molar percentages stated under a), b), c) and d) in each case adding up to 100 mol-%.

A polyesterpolyol having hydroxyl numbers of from 130 to 250, acid numbers of from 10 to 24 and stoichiometrically calculated molecular masses of from 800 to 6000, synthesized from reaction products of

• a) from 15 to 40 mol-% of neopentyl glycol,
• b) from 15 to 35 mol-% of trimethylolpropane,
• c) from 36 to 48 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 2 to 7 mol-% of phthalic acid and/or its anhydride,
• the molar percentages stated under a), b), c) and d) in each case adding up to 100 mol-%.

A polyesterpolyol having hydroxyl numbers of from 130 to 250, acid numbers of from 10 to 24 and stoichiometrically calculated molecular masses of from 600 to 6000, synthesized from reaction products of

• a) from 25 to 40 mol-% of neopentyl glycol,
• b) from 18 to 28 mol-% of trimethylolpropane,
• c) from 35 to 45 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 2 to 5 mol-% of phthalic acid and/or its anhydride,
• the molar percentages stated under a), b), c) and d) in each case adding up to 100 mol-%.

A polyesterpolyol having hydroxyl numbers of from 75 to 250, acid numbers of from 10 to 24 and stoichiometrically calculated molecular masses of from 600 to 2600, synthesized from reaction products of

• a) from 25 to 42 mol-% of neopentyl glycol,
• b) from 5 to 28 mol-% of trimethylolpropane,
• c) from 35 to 46 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 2 to 15 mol-% of phthalic acid and/or its anhydride,
• the molar percentages stated under a), b), c) and d) in each case adding up to 100 mol-%.

A polyesterpolyol having hydroxyl numbers of from 180 to 250, acid numbers of from 10 to 20 and stoichiometrically calculated molecular masses of from 750 to 1500, synthesized from reaction products of

• a) from 26 to 30 mol-% of neopentyl glycol,
• b) from 26 to 30 mol-% of trimethylolpropane,
• c) from 38 to 41 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 3 to 8 mol-% of phthalic acid and/or its anhydride,
• the molar percentages stated under a), b), c) and d) in each case adding up to 100 mol-%.

A polyesterpolyol having hydroxyl numbers of from 80 to 260, acid numbers of from 8 to 25 and stoichiometrically calculated molecular masses of from 600 to 2600, synthesized from reaction products of

• a) from 34 to 39 mol-% of neopentyl glycol,
• b) from 12 to 22 mol-% of trimethylolpropane,
• c) from 35 to 46 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 3 to 15 mol-% of phthalic acid and/or its anhydride,
• the molar percentages stated under a), b), c) and d) in each case adding up to 100 mol-%.

A polyesterpolyol having hydroxyl numbers of from 70 to 110, acid numbers of from 9 to 24 and stoichiometrically calculated molecular masses of from 1200 to 1800, synthesized from reaction products of

• a) from 44 to 47 mol-% of neopentyl glycol,
• b) from 4 to 10 mol-% of trimethylolpropane,
• c) from 42 to 45 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 2 to 4 mol-% of phthalic acid and/or its anhydride,
• the molar percentages stated under a), b), c) and d) in each case adding up to 100 mol-%.

A method for producing binder components for two component polyurethane coating material comprising the steps:

• mixing a polyesterpolyol having a hydroxyl number of from 75 to 300, acid numbers of from 5 to 30 and stochiometrically calculated molecular masses of from 600 to 15,000, synthesized from the reaction products of
• a) from 5 to 50 mol-% of neopentyl glycol,
• b) from 5 to 45 mol-% of trimethylolpropane,
• c) from 20 to 51.5 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 0.5 to 32 mol-% of phthalic acid and/or its anhydride,
• e) from 0 to 18 mol-% of other alkanediols selected from a member of the group consisting of 1,2-, 1,3-, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, cyclohexane-1,4-dimethanol, neopenthyl glycol hydroxypivalate, cyclohexanediol, trimethylpentanediol, ethylbutylpropanediol, ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propanediol, dipropylene glycol, and mixtures thereof,
• f) from 0 to 18 mol-% of other dicarboxylic acids and/or hydroxydicarboxylic acids and/or the anhydride thereof, selected from a member of the group consisting of 5-hydroxyisophthalic acid, isophthalic acid, terephthalic acid, tetrachlorophthalic acid, tetrabromophthalic acid, tetrahydrophthalic acid, 1,2-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, 4-methylhexahydrophthalic acid, endomethylenetetrahydrophthalic acid, tricyclodecanedicarboxylic acid, endoethylenehexahydrophthalic acid, camphoric acid (1,2,2-trimethylcyclopentane-1,3-dicarboxylic acid), adipic acid, succinic acid, azelaic acid, sebacic acid, glutaric acid, and mixtures thereof,
• g) from 0 to 16 mole-% of monocarboxylic acids and/or hydroxycarboxylic acids selected from a member of the group consisting of benzoic acid, p-tert-butylbenzoic acid, lauric acid, isononanoic acid, 2,2-dimethylpropionic acid, 2-ethylhexanoic acid, caproic acid, caprylic acid, capric acid, Versatic acid, hexahydrobenzoic acid, hydroxypivalic acid, 3-,4-hydroxybenzoic acid, 2-,3-hydroxy-4-methylbenzoic acid, 2-,3-,4-hydroxybenzoic acid, 2-hydroxy-2-phenylpropionic acid, and mixtures thereof,
• h) from 0 to 14 mol-% of aliphatic and/or cycloaliphatic monoalcohols, the monoalcohols possessing 4 to 18 C atoms,
• the molar percentages stated under a), b), c), and d), and if appropriate e), f), g), and h), in each case adding up to 100 mol-%;
• and
• paint polyisocyanates and also, if desired, the additives and auxiliaries customary in polyurethane coatings technology, in connection with the preparation of coatings on metals, woods, paper, and board and on polymer moldings.

A method for generating reactive coating materials for producing coatings or primer coats comprising the step of:

• mixing
• (A) a polyesterpolyol having hydroxyl numbers of from 75 to 300, acid numbers of from 5 to 30 and stochiometrically calculated molecular masses of from 600 to 15,000, synthesized from the reaction products of
• a) from 5 to 50 mol-% of neopentyl glycol,
• b) from 5 to 45 mol-% of trimethylolpropane,
• c) from 20 to 51.5 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 0.5 to 32 mol-% of phthalic acid and/or its anhydride,
• e) from 0 to 18 mol-% of other alkanediols selected from a member of the group consisting of 1,2-, 1,3-, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, cyclohexane-1,4-dimethanol, neopentyl glycol hydroxypivalate, cyclohexanediol, trimethylpentanediol, ethylbutylpropanediol, ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propanediol, dipropylene glycol, and mixtures thereof,
• f) from 0 to 18 mol-% of other dicarboxylic acids and/or hydroxydicarboxylic acids and/or the anhydride thereof, selected from a member of the group consisting of 5-hydroxyisophthalic acid, isophthalic acid, terephthalic acid, tetrachlorophthalic acid, tetrabromophthalic acid, tetrahydrophthalic acid, 1,2-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, 4-methylhexahydrophthalic acid, endomethylenetetrahydrophthalic acid, tricyclodecanedicarboxylic acid, endoethylenehexahydrophthalic acid, camphoric acid (1,2,2-trimethylcyclopentane-1,3-dicarboxylic acid), adipic acid, succinic acid, azelaic acid, sebacic acid, glutaric acid, and mixtures thereof,
• g) from 0 to 16 mole-% of monocarboxylic acids and/or hydroxycarboxylic acids selected from a member of the group consisting of benzoic acid, p-tert-butylbenzoic acid, lauric acid, isononanoic acid, 2,2-dimethylpropionic acid, 2-ethylhexanoic acid, caproic acid, caprylic acid, capric acid, Versatic acid, hexahydrobenzoic acid, hydroxypivalic acid, 3-,4-hydroxybenzoic acid, 2-,3-hydroxy-4-methylbenzoic acid, 2-,3-,4-hydroxybenzoic acid, 2-hydroxy-2-phenylpropionic acid, and mixtures thereof,
• h) from 0 to 14 mol-% of aliphatic and/or cycloaliphatic monoalcohols, the monoalcohols possessing 4 to 18 C atoms, the molar percentages stated under a), b), c), and d), and if appropriate e), f), g), and h), in each case adding up to 100 mol-%,
• (B) if desired, other organic polyhydroxy compounds,
• (C) polyisocyanates as hardeners,
• (D) inert organic solvents and, if desired,
• (E) further additives customary in reactive coating materials.

A method for producing coatings or primer coats comprising the step of:

• applying a coating material based on hydroxyl bearing compounds, polyisocyanates, inert solvents and, if desired, customary additives to a support and curing the coating material at room temperature or at an elevated temperature up to 120° C.;
• and
• using polyesterpolyol having hydroxyl numbers of from 75 to 300, acid numbers of from 5 to 30 and stochiometrically calculated molecular masses of from 600 to 15,000, synthesized from the reaction products of
• a) from 5 to 50 mol-% of neopentyl glycol,
• b) from 5 to 45 mol-% of trimethylolpropane,
• c) from 20 to 51.5 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 0.5 to 32 mol-% of phthalic acid and/or its anhydride,
• e) from 0 to 18 mol-% of other alkanediols selected from a member of the group consisting of 1,2-, 1,3-, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, cyclohexane-1,4-dimethanol, neopentyl glycol hydroxypivalate, cyclohexanediol, trimethylpentanediol, ethylbutylpropanediol, ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propanediol, dipropylene glycol, and mixtures thereof,
• f) from 0 to 18 mol-% of other dicarboxylic acids and/or hydroxydicarboxylic acids and/or the anhydride thereof, selected from a member of the group consisting of 5-hydroxyisophthalic acid, isophthalic acid, terephthalic acid, tetrachlorophthalic acid, tetrabromophthalic acid, tetrahydrophthalic acid, 1,2-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, 4-methylhexahydrophthalic acid, endomethylenetetrahydrophthalic acid, tricyclodecanedicarboxylic acid, endoethylenehexahydrophthalic acid, camphoric acid (1,2,2-trimethylcyclopentane-1,3-dicarboxylic acid), adipic acid, succinic acid, azelaic acid, sebacic acid, glutaric acid, and mixtures thereof,
• g) from 0 to 16 mole-% of monocarboxylic acids and/or hydroxycarboxylic acids selected from a member of the group consisting of benzoic acid, p-tert-butylbenzoic acid, lauric acid, isononanoic acid, 2,2-dimethylpropionic acid, 2-ethylhexanoic acid, caproic acid, caprylic acid, capric acid, Versatic acid, hexahydrobenzoic acid, hydroxypivalic acid, 3-,4-hydroxybenzoic acid, 2-,3-hydroxy-4-methylbenzoic acid, 2-,3-,4-hydroxybenzoic acid, 2-hydroxy-2-phenylpropionic acid, and mixtures thereof,
• h) from 0 to 14 mol-% of aliphatic and/or cycloaliphatic monoalcohols, the monoalcohols possessing 4 to 18 C atoms,
• the molar percentages stated under a), b), c), and d), and if appropriate e), f), g), and h), in each case adding up to 100 mol-%, in connection with the applying step.

A method for producing coatings or primer coats comprising the step of:

• employing a proportion of polyisocyanate crosslinker having from 0.5 to 1.5 isocyanate groups to one hydroxyl group in a binder mixture, mixing
• polyesterpolyol having hydroxyl numbers of from 75 to 300, acid numbers of from 5 to 30 and stochiometrically calculated molecular masses of from 600 to 15,000, synthesized from the reaction products of
• a) from 5 to 50 mol-% of neopentyl glycol,
• b) from 5 to 45 mol-% of trimethylolpropane,
• c) from 20 to 51.5 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 0.5 to 32 mol-% of phthalic acid and/or its anhydride,
• e) from 0 to 18 mol-% of other alkanediols selected from a member of the group consisting of 1,2-, 1,3-, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, cyclohexane-1,4-dimethanol, neopentyl glycol hydroxypivalate, cyclohexanediol, trimethylpentanediol, ethylbutylpropanediol, ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propanediol, dipropylene glycol, and mixtures thereof,
• f) from 0 to 18 mol-% of other dicarboxylic acids and/or hydroxydicarboxylic acids and/or the anhydride thereof, selected from a member of the group consisting of 5-hydroxyisophthalic acid, isophthalic acid, terephthalic acid, tetrachlorophthalic acid, tetrabromophthalic acid, tetrahydrophthalic acid, 1,2-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, 4-methylhexahydrophthalic acid, endomethylenetetrahydrophthalic acid, tricyclodecanedicarboxylic acid, endoethylenehexahydrophthalic acid, camphoric acid (1,2,2-trimethylcyclopentane-1,3-dicarboxylic acid), adipic acid, succinic acid, azelaic acid, sebacic acid, glutaric acid, and mixtures thereof,
• g) from 0 to 16 mole-% of monocarboxylic acids and/or hydroxycarboxylic acids selected from a member of the group consisting of benzoic acid, p-tert-butylbenzoic acid, lauric acid, isononanoic acid, 2,2-dimethylpropionic acid, 2-ethylhexanoic acid, caproic acid, caprylic acid, capric acid, Versatic acid, hexahydrobenzoic acid, hydroxypivalic acid, 3-,4-hydroxybenzoic acid, 2-,3-hydroxy-4-methylbenzoic acid, 2-,3-,4-hydroxybenzoic acid, 2-hydroxy-2-phenylpropionic acid, and mixtures thereof,
• h) from 0 to 14 mol-% of aliphatic and/or cycloaliphatic monoalcohols, the monoalcohols possessing 4 to 18 C atoms,
• the molar percentages stated under a), b), c), and d), and if appropriate e), f), g), and h), in each case adding up to 100 mol-%, and polyisocyanate;
• reacting excess isocyanate groups with moisture;
• contributing to the crosslinking with isocyanate groups having reacted with moisture;
• using a polyisocyanate selected from the group consisting of aliphatic polyisocyanates, cycloaliphatic polysisocyanates, capped polyisocyanates, and mixtures thereof.

A method for producing coatings or primer coats comprising the step of:

• employing a proportion of polyisocyanate crosslinker having from 0.5 to 2 isocyanate groups to one hydroxyl group in a binder mixture, mixing
• polyesterpolyol having hydroxyl numbers of from 75 to 300, acid numbers of from 5 to 30 and stochiometrically calculated molecular masses of from 600 to 15,000, synthesized from the reaction products of
• a) from 5 to 50 mol-% of neopentyl glycol,
• b) from 5 to 45 mol-% of trimethylolpropane,
• c) from 20 to 51.5 mol-% of hexahydrophthalic acid and/or its anhydride,
• d) from 0.5 to 32 mol-% of phthalic acid and/or its anhydride,
• e) from 0 to 18 mol-% of other alkanediols selected from a member of the group consisting of 1,2-, 1,3-, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, cyclohexane-1,4-dimethanol, neopentyl glycol hydroxypivalate, cyclohexanediol, trimethylpentanediol, ethylbutylpropanediol, ethylene glycol, diethylene glycol, triethylene glycol, 1,2-propanediol, dipropylene glycol, and mixtures thereof,
• f) from 0 to 18 mol-% of other dicarboxylic acids and/or hydroxydicarboxylic acids and/or the anhydride thereof, selected from a member of the group consisting of 5-hydroxyisophthalic acid, isophthalic acid, terephthalic acid, halo acid, tetrachlorophthalic acid, tetrabromophthalic acid, tetrahydrophthalic acid, 1,2-cyclohexanedicarboxylic acid, 1,4-cyclohexanedicarboxylic acid, 4-methylhexahydrophthalic acid, endomethylenetetrahydrophthalic acid, tricyclodecanedicarboxylic acid, endoethylenehexahydrophthalic acid, camphoric acid (1,2,2-trimethylcyclopentane-1,3-dicarboxylic acid), adipic acid, succinic acid, azelaic acid, sebacic acid, glutaric acid, and mixtures thereof,
• g) from 0 to 16 mole-% of monocarboxylic acids and/or hydroxycarboxylic acids selected from a member of the group consisting of benzoic acid, p-tert-butylbenzoic acid, lauric acid, isononanoic acid, 2,2-dimethylpropionic acid, 2-ethylhexanoic acid, caproic acid, caprylic acid, capric acid, Versatic acid, hexahydrobenzoic acid, hydroxypivalic acid, 3-,4-hydroxybenzoic acid, 2-,3-hydroxy-4-methylbenzoic acid, 2-,3-,4-hydroxybenzoic acid, 2-hydroxy-2-phenylpropionic acid, and mixtures thereof,
• h) from 0 to 14 mol-% of aliphatic and/or cycloaliphatic monoalcohols, the monoalcohols possessing 4 to 18 C atoms,
• the molar percentages stated under a), b), c), and d), and if appropriate e), f), g), and h), in each case adding up to 100 mol-%, and polyisocyanate;
• applying the mixture obtained within a processing time of from about 2 to 48 hours.