Single-component coating material for food containers

Abstract

The invention relates to a single-component coating material for food containers, comprising: a) at least one blocked polyisocyanate containing two or more 2-carbamoylpropane-1,2,3-tricarboxylate structures; b) at least one binder which is reactive toward isocyanate groups and has, on a statistical average, at least two isocyanate-reactive groups per molecule; c) optionally catalysts; and d) optionally solvents and / or optionally auxiliaries and additives; wherein a) and b) are present in an equivalent ratio of the sum of the blocked and non-blocked isocyanate groups from a) to isocyanate-reactive groups from b) of 1.5 : 1 to 12.0 : 1. The invention further relates to the use thereof and to methods for producing aqueous, solvent-free or solvent-containing lacquers, paints, adhesives and molded articles, as well as to the corresponding products.

Description

[0001] 2024PF30029 - Abroad - 1 -One-Component Coating Agent for Food Containers The present invention relates to a one-component coating agent (hereinafter also referred to as a 1K system or 1K-PUR system) for food containers, as well as its use and a method for producing coatings for food containers and the corresponding coated products. The use of blocking agents for the temporary deactivation of isocyanate groups has been known for a long time. Blocked polyisocyanates are used, among other things, for the production of room-temperature stable 1K-PUR systems that begin to crosslink when the blocking agent's deblocking temperature is reached. The blocked polyisocyanates are reacted with typical isocyanate-reactive compounds. 1K-PUR coatings are currently used in can and coil coating, automotive primary coating, and plastic coating.Depending on the requirements, various polyisocyanates based on aliphatic diisocyanates are used. Examples include the linear aliphatic diisocyanates hexamethylene diisocyanate (HDI) and pentamethylene diisocyanate (PDI), or the cycloaliphatic diisocyanates isophorone diisocyanate (IPDI) and 4,4'-diisocyanatodicyclohexylmethane ("H12MDI"). Food containers are often coated with internal layers, which, for example, act as a protective layer in metallic containers, remaining in direct contact with the food or beverages inside for extended periods. The most commonly used blocking agents for isocyanates are ε-caprolactam and MEKO. While in the case of ε-caprolactam, baking temperatures of around 170°C or higher are usually used, blocked 1K-PUR stoving lacquers, in which MEKO was used as a blocking agent, can be baked at temperatures 10 to 20°C lower.However, MEKO is disadvantageous due to its toxicological properties and cannot be used in coatings for food containers. Furthermore, many blocking agents are based entirely on fossil raw materials, which is another disadvantage of blocking agents known in the prior art, and the high curing temperatures of ε-caprolactam-blocked systems are energetically disadvantageous. The present invention was therefore based on the objective of providing a one-component coating agent for food containers that leads to flexible coatings with excellent resistance in sterilization tests even at curing temperatures of 150 to 160 °C. This objective was achieved by providing a one-component coating agent for food containers, comprising 2024PF30029 - Abroad. - 2 -a) at least one blocked polyisocyanate containing two or more 2-carbamoylpropane-1,2,3-tricarboxylate structures, b) at least one binder reactive towards isocyanate groups with, on average, at least two isocyanate-reactive groups per molecule, c) optionally catalysts, and d) optionally solvents and / or optionally excipients and additives, wherein a) and b) are present in an equivalent ratio of the sum of blocked and unblocked isocyanate groups from a) to isocyanate-reactive groups from b) of 1.5 : 1 to 12.0 : 1. Surprisingly, it has been found that triesters of citric acid (also referred to as "citrates" within the scope of the invention) can be used as blocking agents for isocyanates and, in addition to lower viscosity, also offer the further advantages of lower crosslinking or...The curing temperature is reduced while maintaining improved flexibility and sterilization resistance of the coatings for food containers obtainable from the one-component coating materials according to the invention. Preferably, the terms "comprising" or "containing," "essentially consisting of," and particularly preferably "consisting of." The further embodiments mentioned in the claims and in the description can be combined as desired, unless the context clearly indicates otherwise. "At least one," as used herein, refers to one or more, for example, two, three, four, five, six, seven, eight, nine, or more. In connection with components of the compounds described herein, this term refers not to the absolute quantity of molecules but to the type of component.“At least one blocked polyisocyanate” therefore means, for example, that only one type of blocked polyisocyanate or several different types of blocked polyisocyanates may be included, without specifying the quantity of each compound. Numerical values ​​given herein without decimal places refer to the full value given with one decimal place. For example, “99%” means “99.0%”. Numerical ranges given in the format “in / from x to y” include the values ​​mentioned. If several preferred numerical ranges are given in this format, it is understood that all ranges resulting from the combination of the different endpoints are also included. For the purposes of this document, the term “aliphatic” is defined as non-aromatic hydrocarbon groups that are branched or unbranched and, in each case, saturated or unsaturated. 2024PF30029 - Foreign. - 3 -For the purposes of this document, the term "alicyclic" or "cycloaliphatic" is defined as, where applicable, substituted, carbocyclic or heterocyclic compounds or units that are non-aromatic (such as cycloalkanes, cycloalkenes, or oxa-, thia-, aza-, or thiazacycloalkanes). Specific examples include cyclohexyl groups, cyclopentyl groups, and their N- or O-heterocyclic derivatives, such as pyrimidine, pyrazine, tetrahydropyran, or tetrahydrofuran. For the purposes of this document, the term "araliphatic" is defined as aliphatic hydrocarbon residues that are saturated or unsaturated and contain at least one aromatic substituent.In the event that the groups or compounds are disclosed as "optionally substituted" or "substituted", suitable substituents are -F, -Cl, -Br, -I, -OH, -OCH3, -OCH2CH3, -O-isopropyl or -one-propyl, -OCF3, -CF3, -S-C1-6-alkyl and / or (optionally via an attached heteroatom) a linear or branched, aliphatic and / or alicyclic structural unit with 1 to 12 carbon atoms, each acting as a replacement for a carbon-bound hydrogen atom of the molecule in question. Preferred substituents are halogen (in particular -F, -Cl), C1-6-alkoxy (in particular methoxy and ethoxy), hydroxy, trifluoromethyl and trifluoromethoxy, each acting as a replacement for a carbon-bound hydrogen atom of the molecule in question.Polyisocyanates A) for the at least one blocked polyisocyanate a) are any diisocyanates, triisocyanates and / or polyisocyanates with aliphatic, cycloaliphatic, araliphatic and / or aromatically bonded isocyanate groups. Suitable diisocyanates and triisocyanates A) are any diisocyanates and triisocyanates accessible in various ways, for example by phosgenation of the corresponding diamines or triamines, which can be produced using fossil raw materials or renewable raw materials, optionally using mass balance, in the liquid or gas phase or by phosgene-free means, such as thermal urethane cleavage, preferably those in the molecular weight range of 140 to 400 with aliphatic, cycloaliphatic, araliphatic and / or aromatically bonded isocyanate groups, such as...1,4-Diisocyanatobutane, 1,5-Diisocyanatopentane (PDI), 1,6-Diisocyanatohexane (HDI), 2-Methyl-1,5-diisocyanatopentane, 1,5-Diisocyanato-2,2-dimethylpentane, 2,2,4- and 2,4,4-Trimethyl-1,6-diisocyanatohexane, 1,8-Diisocyanatooctane, 1,9-Diisocyanatononane, 1,10-Diisocyanatodecane, 1,3- and 1,4-Diisocyanatocyclohexane, 1,3- and 1,4-Bis-(isocyanatomethyl)cyclohexane, 1-Isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane (Isophorone diisocyanate, IPDI), 2,4'- and 4,4'-Diisocyanatodicyclohexylmethane (H12-MDI) 4,4'-Diisocyanato-3,3'-dimethyldicyclohexylmethane, 4,4'-Diisocyanato-3,3',5,5'-tetramethyldicyclohexylmethane, 4,4'-Diisocyanato-1,1'-bi(cyclohexyl), 4,4'-Diisocyanato-3,3'-dimethyl-1,1'-bi(cyclohexyl), 4,4'-Diisocyanato-2,2',5,5'-2024PF30029 - Foreign countries. - 4 -tetra-methyl-1,1'-bi(cyclohexyl), 1,8-diisocyanato-p-menthane, 1,3-diisocyanatoadamantane, 1,3-dimethyl-5,7-diisocyanatoadamantane, 1-isocyanato-1-methyl-4(3)isocyanato-methylcyclohexane, bis-(isocyanatomethyl)norbornane (NBDI), 4-isocyanatomethyl-1,8-octanediisocyanate (triisocyanatoonane; TIN), 1,3- and 1,4-bis(isocyanatomethyl)benzene (xylylene diisocyanate, XDI), 1,3- and 1,4-bis-(2-isocyanato-prop-2-yl)benzene (TMXDI), 1,3-bis(isocyanatomethyl)-4-methylbenzene, 1,3-bis(isocyanatomethyl)-4-ethylbenzene, 1,3- Bis(isocyanatomethyl)-5-methylbenzene, 1,3-Bis(isocyanatomethyl)-4,5-dimethylbenzene, 1,4-Bis(isocyanatomethyl)-2,5-dimethylbenzene, 1,4-Bis(isocyanatomethyl)-2,3,5,6-tetramethylbenzene, 1,3-Bis(isocyanatomethyl)-5-tert-butylbenzene, 1,3-Bis(isocyanatomethyl)-4-chlorobenzene, 1,3-Bis(isocyanatomethyl)-4,5-dichlorobenzene, 1,3-Bis(isocyanatomethyl)-2,4,5,6-tetrachlorobenzene, 1,4-Bis(isocyanatomethyl)-2,3,5,6-tetrachlorobenzene, 1,4-Bis(isocyanatomethyl)-2,3,5,6-tetrabromobenzene, 1,4-Bis(2-isocyanatoethyl)benzene and 1,4-bis(isocyanatomethyl)naphthalene, 1,2-, 1,3- and 1,4-diisocyanatobenzene (phenylene diisocyanate), 2,4- and 2,6-diisocyanatotoluene (TDI), 2,3,5,6-tetramethyl-1,4-diisocyanatobenzene, the isomeric diethylphenylene diisocyanates, diisopropylphenylene diisocyanates, diisododecylphenylene diisocyanates and biphenyl diisocyanates, 3,3'-dimethoxybiphenyl-4,4'-diisocyanate, 2,2'-, 2,4'- and 4,4'-diisocyanatodiphenylmethane (MDI), 3,3'-dimethyldiphenylmethane-4,4'-diisocyanate, 4,4'-diisocyanatodiphenylethane, 1,5-diisocyanatonaphthalene (Naphthylene diisocyanate, NDI), diphenyl ether diisocyanate, ethylene glycol diphenyl ether diisocyanate, diethylene glycol diphenyl ether diisocyanate, 1,3-propylene glycol diphenyl ether diisocyanate, benzophenone diisocyanate, triisocyanatobenzene, 2,4,6-triisocyanatotoluene, trimethylbenzene triisocyanate, Diphenylmethane-2,4,4'-triisocyanate, 3-methyldiphenylmethane-4,6,4'-triisocyanate, the isomeric naphthalene triisocyanates and methylnaphthalene diisocyanates,Triphenylmethane triisocyanate, 2,4-diisocyanato-1-[(5-isocyanato-2-methylphenyl)methyl]benzene, or mixtures of at least two such diisocyanates and triisocyanates. Suitable polyisocyanates A) are any polyisocyanates prepared by modifying simple aliphatic, cycloaliphatic, araliphatic, and / or aromatic diisocyanates and / or triisocyanates, for example, those of the type mentioned above, with uretdione, isocyanurate, allophanate, biuret, iminooxadiazindione, and / or oxadiazinetrione structures, as described, for example, in J. Prakt. Chem.336 (1994) 185 - 200, in DE-A 1670666, DE-A 1954093, DE-A 2414413, DE-A 2452532, DE-A 2641380, DE-A 3700 209, DE-A 3900053 and DE-A 3928503 or in EP-A 0336205, EP-A 0339396, EP-A 0798299, EP-A 0962454, EP-A 0962455, EP-A 2785760, EP-A 2883895, EP-A 3107922, EP-A 3 107 948 and EP-A 3 337 836 by way of example are described or any mixtures of such polyisocyanates. 2024PF30029 - Abroad, - 5 -If necessary, when modifying the aforementioned diisocyanates and / or triisocyanates to polyisocyanates A), monoisocyanates, particularly those with a molecular weight in the range of 99 to 300, such as n-butyl isocyanate, n-amyl isocyanate, n-hexyl isocyanate, n-heptyl isocyanate, n-octyl isocyanate, undecyl isocyanate, dodecyl isocyanate, tetradecyl isocyanate, cetyl isocyanate, stearyl isocyanate, cyclopentyl isocyanate, cyclohexyl isocyanate, 3- or 4-methylcyclohexyl isocyanate, benzyl isocyanate, phenyl isocyanate, or naphtyl isocyanate, may also be used in subordinate quantities. If used at all, monoisocyanates are employed in amounts of up to 30 wt.%, preferably up to 20 wt.%, and particularly preferably up to 10 wt.%, based on the total amount of mono-, di-, and triisocyanates.In the production of the polyisocyanates A), the actual modification reaction is generally followed by a further process step for the separation of the unreacted excess monomeric diisocyanates and / or triisocyanates and, if applicable, monoisocyanates. This monomer separation is carried out according to methods known per se, preferably by thin-film distillation under vacuum or by extraction with suitable solvents inert to isocyanate groups, for example, aliphatic or cycloaliphatic hydrocarbons such as pentane, hexane, heptane, cyclopentane, or cyclohexane. In a first preferred embodiment of the one-component coating agent for food containers according to the invention, the blocked polyisocyanate a) additionally contains one or more isocyanurate, allophane, urethane, urea, uretdione, iminooxadiazindione, oxadiazinetrione, and / or biuret structures.Preferably, the starting material of the blocked polyisocyanate a) as polyisocyanate A) polyisocyanates, preferably polyisocyanates of the type mentioned, are used, which have an isocyanate group content of 6.0 to 26.0 wt.%, preferably of 8.0 to 25.0 wt.%, particularly preferably 10.0 to 24.0 wt.%, and / or a monomeric diisocyanate content of less than 0.50 wt.%, preferably less than 0.30 wt.%, more preferably less than 0.20 wt.%, particularly preferably less than 0.10 wt.%. For the alternative, optional case that triisocyanates and / or monoisocyanates were used to produce the polyisocyanates A), the aforementioned residual monomer contents of less than 0.50 wt.%, preferably less than 0.30 wt.%, more preferably less than 0.20 wt.%, and particularly preferably less than 0.10 wt.%, refer to all diisocyanates, triisocyanates and monoisocyanates used.NCO content is determined according to DIN EN ISO 11909:2007-05, and residual monomer content according to DIN EN ISO 10283:2007-11, by gas chromatography with an internal standard. 2024PF30029 - Foreign. - 6 -Particularly preferred polyisocyanates A) are those of the type mentioned above with exclusively aliphatic and / or cycloaliphatic bonded isocyanate groups. Most preferred polyisocyanates A) are polyisocyanates containing at least isocyanurate structures based on 1,5-diisocyanatopentane, 1,6-diisocyanatohexane, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane, 1,3-bis(isocyanatomethyl)benzene, bis-(isocyanatomethyl)norbornane, and / or 4,4'-diisocyanatodicyclohexylmethane. Alternatively or in combination, the polyisocyanates A) preferably have an average NCO functionality of 2.0 to 5.0, preferably 2.5 to 4.5. The average NCO functionalities are determined by gel permeation chromatography. Preferably, the free NCO content of the blocked polyisocyanate is a) ≤ 5 wt%, preferably ≤ 2 wt%, particularly preferably ≤ 1 wt%, even more preferably ≤ 0.5 wt% and most preferably ≤ 0.3 wt%.-%, determined by titration according to DIN EN ISO 11909:2007-05 and based on the total weight of the blocked polyisocyanate a). The blocked polyisocyanates a) can be identified, for example, by NMR spectrometry or HPLC-MS through qualitative and quantitative determination of the 2-carbamoylpropane-1,2,3-tricarboxylate structures. In a further preferred embodiment of the one-component coating agent for food containers according to the invention, the two or more 2-carbamoylpropane-1,2,3-tricarboxylate structures of the blocked polyisocyanate a) have a general formula (I). (I) in which R independently represents any saturated or unsaturated, linear or branched aliphatic residue with 1 to 18 carbon atoms, saturated or unsaturated cycloaliphatic residue with 3 to 18 carbon atoms, araliphatic residue with 7 to 18 carbon atoms, and / or aromatic residue with 6 to 18 carbon atoms, each of which is substituted or unsubstituted and / or has heteroatoms in the chain. In a further preferred embodiment of the one-component coating agent for food containers according to the invention, the two or more 2-carbamoylpropane-1,2,3-tricarboxylate structures of the blocked polyisocyanate have a) a general formula (I),2024PF30029 - Abroad - 7 - (I) in which R independently represents any saturated or unsaturated, linear or branched aliphatic residue with 1 to 8 carbon atoms and / or saturated or unsaturated cycloaliphatic residue with 5 to 8 carbon atoms, each being substituted or unsubstituted and / or having heteroatoms in the chain, preferably in which R independently represents any saturated or unsaturated, linear or branched aliphatic residue with 1 to 4 carbon atoms, each being substituted or unsubstituted and / or having heteroatoms in the chain, particularly preferably in which R independently represents any saturated or unsaturated, linear or branched aliphatic residue with 2 to 4 carbon atoms.The carbamoylpropane-1,2,3-tricarboxylate structures, and thus also the structures of general formula (I), represent the blocked NCO groups, with a corresponding citrate acting as the blocking agent. Since blocking agents are always used in large quantities to block essentially all free isocyanate groups, citrates offer the ecological advantage of being available on an industrial scale from (partially) bio-based raw materials. The blocked polyisocyanate a) can be prepared by a manufacturing process comprising the reaction of at least one polyisocyanate A) with at least one citrate B), optionally in the presence of at least one catalyst, wherein the citrate B) is used in an amount of ≥ 95 equivalent % based on the isocyanate groups of the polyisocyanate A). The suitable and preferred polyisocyanates A) are those described above.Preferably in the manufacturing process, the at least one polyisocyanate A) has aliphatic, cycloaliphatic, araliphatic and / or aromatically bonded isocyanate groups and / or preferably comprises one or more polyisocyanates containing isocyanurate structures based on 1,5-diisocyanatopentane, 1,6-diisocyanatohexane, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane, 1,3-bis(isocyanatomethyl)benzene, bis-(isocyanatomethyl)norbornane and / or 4,4'-diisocyanatodicyclohexylmethane. The citrate B) is preferably used in an amount of ≥ 98 equivalent-%, particularly preferably ≥ 99 equivalent-%, even more preferably ≥ 99.5 equivalent-% and most preferably ≥ 99.7 equivalent-%, based on the isocyanate groups of the polyisocyanate A). 2024PF30029 - Foreign. - 8 - The at least one citrate (B) can be selected from various compounds. Preferably, in the manufacturing process, the at least one citrate (B) is one of the general formula (II). (II), in which R independently represents any saturated or unsaturated, linear or branched aliphatic residue with 1 to 18 carbon atoms, saturated or unsaturated cycloaliphatic residue with 3 to 18 carbon atoms, araliphatic residue with 7 to 18 carbon atoms and / or aromatic residue with 6 to 18 carbon atoms, each being substituted or unsubstituted and / or having heteroatoms in the chain. Particularly preferred in the manufacturing process is the at least one citrate B), one of the general formula (II), (II), in which R independently represents any saturated or unsaturated, linear or branched aliphatic residue with 1 to 8 carbon atoms and / or saturated or unsaturated cycloaliphatic residue with 5 to 8 carbon atoms, each being substituted or unsubstituted and / or having heteroatoms in the chain, preferably in which R independently represents any saturated or unsaturated, linear or branched aliphatic residue with 1 to 4 carbon atoms, each being substituted or unsubstituted and / or having heteroatoms in the chain, particularly preferably in which R independently represents any saturated or unsaturated, linear or branched aliphatic residue with 2 to 4 carbon atoms.Beispielhafte geeignete und bevorzugte Citrate B) sind Trimethylcitrat, Triethylcitrat, Tri-n- propylcitrat, Tri-iso-propylcitrat, Tri-n-butylcitrat, Tri-sec-butylcitrat, Tri-iso-butylcitrat, Tri-tert- butylcitrat, Tri-n-pentylcitrat, Tri(2-pentyl)citrat, Tri(3-pentyl)citrat, Tri(2-methyl-1-butyl)citrat , Tri(2-methyl-2-butyl)citrat, Tri-(3-methyl-1-butyl)citrat, Tri(3-methyl-2-butyl)citrat, Tri(2,2- Dimethyl-1-propyl)citrat, Tri-n-hexylcitrat, Tri(2-hexyl)citrat, Tri(3-hexyl)citrat, Tri(2-methyl-1- pentyl)citrat, Tri(2-methyl-2-pentyl)citrat, Tri(2-methyl-3-pentyl)citrat, Tri(4-methyl-1-2024PF30029 - Ausland. - 9 -pentyl)citrat, Tri(4-methyl-2-pentyl)citrat, Tri(3-methyl-1-pentyl)citrat, Tri(3-methyl-2- pentyl)citrat, Tri(3-methyl-3-pentyl)citrat, Tri(2,2-dimethyl-1-butyl)citrat, Tri(3,3-dimethyl-1- butyl)citrat, Tri(3,3-dimethyl-2-butyl)citrat, Tri(2,3-dimethyl-1-butyl)citrat, Tri(2,3-dimethyl-2-butyl)citrat, Tri(2-ethyl-1-butyl)citrat, Tri-n-heptylcitrat, Tri-(2-heptyl)citrat, Tri-(3-heptyl)citrat,Tri-(4-heptyl)citrat, Tri(5-methyl-1-hexyl)citrat, Tri(5-methyl-2-hexyl)citrat, Tri(5-methyl-3- hexyl)citrat, Tri(2-methyl-3-hexyl)citrat, Tri(2-methyl-2-hexyl)citrat, Tri(2-methyl-1-hexyl)citrat, Tri(4-methyl-1-hexyl)citrat, Tri(4-methyl-2-hexyl)citrat, Tri(4-methyl-3-hexyl)citrat, Tri(3- methyl-3-hexyl)citrat, Tri(3-methyl-2-hexyl)citrat, Tri(3-methyl-1-hexyl)citrat, Tri(2-ethyl-1- pentyl)citrat, Tri(3-ethyl-1-pentyl)citrat, Tri(3-ethyl-2-pentyl)citrat, Tri(3-ethyl-3-pentyl)citrat, Tri(3,4-dimethyl-1-pentyl)citrat, Tri(3,4-dimethyl-2-pentyl)citrat, Tri(2,3-dimethyl-1-pentyl)citrat, Tri(2,3-dimethyl-2-pentyl)citrat,Tri(2,3-dimethyl-3-pentyl)citrat, Tri(2-isopropyl-1-butyl)citrat, Tri(2,3,3-trimethyl-1-butyl)citrat); Tri(2,2,3-trimethyl-1-butyl)citrat); Tri(2,3,3-trimethyl-2- butyl)citrat), Tri(3,3-dimethyl-1-pentyl)citrat, Tri(3,3-dimethyl-2-pentyl)citrat, Tri(2-ethyl- 2methyl-1-butyl)citrat, Tri(4,4-dimethyl-1-pentyl)citrat, Tri(4,4-dimethyl-2-pentyl)citrat, Tri(2,2- dimethyl-1-pentyl)citrat, Tri-n-octylcitrat, Tri(2-octyl)citrat, Tri(3-octyl)citrat), Tri(4-octyl)citrat, Tri(2-methyl-1-heptyl)citrat, Tri(2-methyl-2-heptyl)citrat, Tri(2-methyl-3-heptyl)citrat, Tri(2- methyl-4-heptyl)citrat, Tri(3-methyl-1-heptyl)citrat, Tri(3-methyl-2-heptyl)citrat, Tri(3-methyl-3- heptyl)citrat, Tri(3-methyl-4-heptyl)citrat, Tri(4-methyl-1-heptyl)citrat,, Tri(4-methyl-3- heptyl)citrat, Tri(4-methyl-4-heptyl)citrat, Tri(5-methyl-1-heptyl)citrat, Tri(5-methyl-2- heptyl)citrat, Tri(5-methyl-3-heptyl)citrat, Tri(6-methyl-1-heptyl)citrat, Tri(6-methyl-2- heptyl)citrat,Tri(6-methyl-3-heptyl)citrat, Tri(2,2-dimethyl-1-hexyl)citrat, Tri(2,2-dimethyl-3- hexyl)citrat, Tri(2,3-dimethyl-1-hexyl)citrat , Tri(2,3-dimethyl-2-hexyl)citrat, Tri(2,3-dimethyl-3- hexyl)citrat, Tri(2,4-dimethyl-1-hexyl)citrat, Tri(2,4-dimethyl-2-hexyl)citrat, Tri(2,4-dimethyl-3- hexyl)citrat Tri(2,5-dimethyl-1-hexyl)citrat, Tri(2,5-dimethyl-2-hexyl)citrat, Tri(2,5-dimethyl-3- hexyl)citrat, Tri(3,3-dimethyl-1-hexyl)citrat, Tri(3,3-dimethyl-2-hexyl)citrat, Tri(3,4-dimethyl-1- hexyl)citrat, Tri(3,4-dimethyl-2-hexyl)citrat, Tri(3,4-dimethyl-3-hexyl)citrat, Tri(3,5-dimethyl-1- hexyl)citrat, Tri(3,5-dimethyl-2-hexyl)citrat,Tri(3,5-dimethyl-3-hexyl)citrat, Tri(4,4-dimethyl-1- hexyl)citrat, Tri(4,4-dimethyl-2-hexyl)citrat, Tri(4,4-dimethyl-3-hexyl)citrat, Tri(4,5-dimethyl-1- hexyl)citrat, Tri(4,5-dimethyl-2-hexyl)citrat, Tri(4,5-dimethyl-3-hexyl)citrat, Tri(5,5-dimethyl-1- hexyl)citrat, Tri(5,5-dimethyl-2-hexyl)citrat, Tri(5,5-dimethyl-3-hexyl)citrat, Tri(2-ethyl-1- hexyl)citrat,Tri(3-ethyl-1-hexyl)citrat, Tri(3-ethyl-2-hexyl)citrat, Tri(3-ethyl-3-hexyl)citrat, Tri(4- ethyl-1-hexyl)citrat, Tri(4-ethyl-2-hexyl)citrat, Tri(4-ethyl-3-hexyl)citrat, Tri(2-propyl-1- pentyl)citrat, Tri(2-ethyl-2-methyl-1-pentyl)citrat, Tri(2-ethyl-3-methyl-1-pentyl)citrat, Tri(2- ethyl-4-methyl-1-pentyl)citrat, Tri(3-ethyl-2-methyl-1-pentyl)citrat, Tri(3-ethyl-2-methyl-2- pentyl)citrat, Tri(3-ethyl-2-methyl-3-pentyl)citrat, , Tri(3-ethyl-3-methyl-1-pentyl)citrat, , Tri(3- ethyl-3-methyl-2-pentyl)citrat, Tri(3-ethyl-4-methyl-1-pentyl)citrat, Tri(3-ethyl-4-methyl-2- pentyl)citrat, Tri(2,2,3-trimethyl-1-pentyl)citrat), Tri(2,2,3-trimethyl-2-pentyl)citrat), Tri(2,2,3-2024PF30029 - Ausland, - 10 -trimethyl-3-pentyl)citrat) , Tri(2,2,4-trimethyl-1-pentyl)citrat), Tri(2,2,4-trimethyl-3-pentyl)citrat), Tri(2,3,3-trimethyl-1-pentyl)citrat), Tri(2,3,3-trimethyl-2-pentyl)citrat), Tri(2,3,4-trimethyl-1-pentyl)citrat), Tri(2,3,4-trimethyl-2-pentyl)citrat), Tri(2,3,4-trimethyl-3-pentyl)citrat), Tri(2,4,4-trimethyl-1-pentyl)citrat), Tri(2,4,4-trimethyl-2-pentyl)citrat), Tri(3,3,4-trimethyl-1-pentyl)citrat), Tri(3,3,4-trimethyl-2-pentyl)citrat), Tri(3,4,4-trimethyl-1-pentyl)citrat), Tri(3,4,4-trimethyl-2- pentyl)citrat),Tri(2-Ethyl-2,3-dimethyl-1-butyl)citrat, Tri(2-Ethyl-3,3-dimethyl-1-butyl)citrat, Tri(3-methyl-2-(1-methylethyl)-1-butyl)citrat, Tri(2,2-diethyl-1-butyl)citrat, Tri(2,2,3,3-Tetramethyl-1-butyl)citrat, Trivinylcitrat, Triallylcitrat, Tri(2-(acryloyloxy)ethyl)citrat,Tri(2-(Methacryloyloxy)ethyl)citrat, Tribenzylcitrat, Triphenylcitrat Tricyclopropylcitrat, Tricyclobutylcitrat, Tricyclopentylcitrat, Tricyclohexylcitrat, Tricycloheptylcitrat,Tricyclooctyl citrate and mixtures thereof. Particularly preferred citrates B) are trimethyl citrate, triethyl citrate, tripropyl citrate, triisopropyl citrate, tri-n-butyl citrate, tri-sec-butyl citrate, tri-isobutyl citrate, tri-tert-butyl citrate, tri-n-pentyl citrate, tri-n-hexyl citrate, tri-n-octyl citrate, tri(2-ethyl-1-hexyl) citrate, and mixtures thereof. Most particularly preferred citrates B) are trimethyl citrate, triethyl citrate, tributyl citrate, and mixtures thereof. If desired, the aforementioned citrates B) can also be mixed-esterified, for example, diethyl methyl citrate or butyl diethyl citrate. Since the citrates B) with the isocyanate groups form the 2-carbamoylpropane-1,2,3-tricarboxylate structures of the blocked polyisocyanates a), the 2-carbamoylpropane-1,2,3-trimethoxylate structures, 2-carbamoylpropane-1,2,3-triethoxylate structures, 2-carbamoylpropane-1,2,3-tributoxylate structures and mixtures of the aforementioned are particularly preferred structures and particularly preferred embodiments of the general formula (I). Citric acid esters such as triethyl citrate, unlike the blocking agents known from the prior art, are not toxic, irritating, or otherwise harmful to health. To carry out the manufacturing process, the at least one polyisocyanate A) is reacted with the at least one citrate B), preferably at temperatures of 20 to 120 °C, particularly preferably at temperatures of 40 to 100 °C, to give the blocked polyisocyanate a). The blocking reaction in the manufacturing process can be carried out thermally induced without a catalyst or in the presence of at least one catalyst. Preferably, the reaction is carried out in the presence of at least one catalyst. This has the advantage of further increasing the efficiency and cost-effectiveness of the manufacturing process. 2024PF30029 - Foreign,- 11 -Suitable catalysts include tertiary amines such as triethylamine, pyridine, methylpyridine, 1,4-diazabicyclo[2.2.2]octane, 1,8-diazabicyclo[5.4.0]undec-7-ene, 1,5-diazabicyclo[4.3.0]non-5-ene, 4-(dimethylamino)pyridine, benzyldimethylamine, N,N-endoethylenepiperazine, N-methylpiperidine, pentamethyldiethylenetriamine, N,N-dimethylaminocyclohexane, N,N'-dimethylpiperazine, but also metal salts and chelates, salts of transition metals, metalloids or inorganic bases, such as potassium carbonate. Preferably, iron(III), bismuth(III), zinc(II), tin(II), tin(IV), zirconium(IV), titanium(IV), molybdenum(VI) and Al(III) are used as catalytically acting metal ions.Examples include iron(III) chloride, bismuth(III) octoate, bismuth(III) triflate, bismuth(III) neodecanoate, aluminum tri(ethyl acetoacetate), zinc(II) chloride, zinc(II) n-octanoate, zinc(II)-2-ethyl-1-hexanoate, zinc 2-ethyl caproate, zinc(II) stearate, Zinc(II) naphtenate, zinc(II) acetylacetonate, tin(II) n-octanoate, tin(II) 2-ethyl-1-hexanoate, tin(II) ethyl caproate, tin(II) laurate, tin(II) palmitate), tin(II) triflate, tin(II) chloride, dibutyltin(IV) oxide, Dibutyltin(IV) dichloride, dibutyltin(IV) diacetate, dibutyltin(IV) dimaleate, Dibutyltin(IV) dilaurate, dioctyltin(IV) diacetate, molybdenum glycolate, tetraisopropyl titanate, tetrabutyl titanate, titanium(IV) acetylacetonate, zirconium(IV) neodecanoate, aluminum trisec butylate, aluminum(III) acetylacetonate, aluminum(III) triflate or any mixtures of such catalysts may be used.The at least one catalyst, if present, is preferably present in the manufacturing process in amounts of 1 to 10,000 ppm, preferably 2 to 5,000 ppm, particularly preferably 5 to 1,000 ppm, and most preferably 10 to 250 ppm. A further advantage of the aforementioned catalysts containing metal ions is that they can be measured qualitatively and quantitatively in the blocked polyisocyanates a) and the one-component coating agent for food containers according to the invention, for example, by means of ICP-OES or ICP-MS. The manufacturing process can be carried out without solvents. However, suitable solvents that are inert to the reactive groups of the polyisocyanates A) can also be used. Suitable solvents for this purpose include those produced using fossil raw materials or renewable raw materials, in particular the conventional paint solvents known per se, such as, for example,Ethyl acetate, butyl acetate, ethylene glycol monomethyl or ethyl ether acetate, 1-methoxypropyl-2-acetate, 3-methoxy-n-butyl acetate, ethyl(-)-L-lactate, acetone, 2-butanone, 4-methyl-2-pentanone, cyclohexanone, dihydrolevoglucosenone, toluene, xylene, chlorobenzene, white spirit, highly substituted aromatics such as those sold under the names solvent naphtha, Solvesso®, Isopar®, Nappar®, Varsol® (ExxonMobil Chemical Central Europe, Cologne, DE) and Shellsol® (Shell Deutschland Oil GmbH, Hamburg, DE), but also solvents such as dimethylfuran, 2-methyltetrahydrofuran, dimethyl isosorbide (DMI), γ-valerolactone, 2024PF30029 - Foreign. - 12 -Propylene glycol diacetate, diethylene glycol dimethyl ether, dipropylene glycol dimethyl ether, diethylene glycol ethyl and butyl ether acetate, N-methylpyrrolidone and N-methylcaprolactam, or any mixtures of such solvents. Following the reaction of the polyisocyanate A) with the citrate B), when the content of free isocyanate groups is preferably 2% or less by weight, more preferably 1% or less by weight, particularly preferably 0.5% or less by weight, and most preferably 0.3% or less by weight, the blocked polyisocyanates a) can optionally be further diluted with solvent, for example, to reduce the viscosity. In addition to the solvents mentioned above, alcoholic solvents, such as n-butanol or isobutyl alcohol, can also be used, since the isocyanate groups will then have reacted largely, preferably completely, with the blocking agent. In the manufacturing process, further auxiliary and additive substances, such as... B.Antioxidants or light stabilizers can be used. These can be added to one or more of the reactants A), B) and optionally to the catalyst before the actual reaction begins. Alternatively, they can be added to the reaction mixture at any time during the reaction or to the blocked polyisocyanates a) after the reaction has taken place. The auxiliary and additive substances described herein as suitable and preferably may also be optionally included as component d) in the one-component coating agent for food containers according to the invention. Suitable antioxidants are, for example, phenols, in particular sterically hindered phenols, such as...2,6-Di-tert-butylphenol, 2,4-Dimethyl-6-tert-butylphenol, 2,6-Di-tert-butyl-4-methylphenol, Triethylene glycol bis(3-tert-butyl-4-hydroxy-5-methylphenyl)propionate, Octadecyl-3-(3,5-di-tert-butyl-4-hydroxy-phenyl)propionate, Pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4-hydroxy-phenyl)propionate), Esters of 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid with aliphatic branched C7 to C9 alcohols, such asIsoheptyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, isooctyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate or isononyl 3-(3,5-di-tert-butyl-4-hydroxyphenylpropionate, Isotridecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, thiodiethyl bis[3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate], N,N'-hexamethylene-bis(3,5-di-tert-butyl-4-hydroxyphenyl)propionic acid amide, 1,2-Bis(3,5-di-tert-butyl-4-hydroxyphenylpropionic acid) hydrazide, 2,4-di-tert-butylphenyl-4'-hydroxy-3',5'-di-tert-butyl benzoate, Esters of (3,5-di-tert-butyl-4-hydroxyphenyl)methylthioacetic acid with aliphatic branched C10 to C14 alcohols, 2,2'-thio-bis(4-methyl-6-tert-butylphenol),2-methyl-4,6-bis(octylthiomethyl)phenol, 1,3,5-trimethyl-2,4,6-tris(3,5-di-tert-butyl-4-2024PF30029 - Abroad. - 13 -hydroxybenzyl)benzene, tris(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate, or 2,5-di-tert-amylhydroquinone. Suitable antioxidants also include thioethers, such as didodecyl-3,3'-thiodipropionate or dioctadecyl-3,3'-thiodipropionate, which are preferably used in combination with phenolic antioxidants of the aforementioned type. Other suitable antioxidants are phosphites, for example, di- or preferably trisubstituted phosphites, such as... B. Dibutyl phosphite, dibenzyl phosphite, triethyl phosphite, tributyl phosphite, triisodecyl phosphite, trilauryl phosphite, tris (tridecyl) phosphite, triphenyl phosphite, tris (2,4-di-tert-butylphenyl) phosphite, tris (nonylphenyl) phosphite, Diphenyl isooctyl phosphite, diphenyl isodecyl phosphite, diisodecyl phenyl phosphite, diisooctyl octylphenyl phosphite, phenyl neopentyl glycol phosphite, 2,4,6-tri-tert-butylphenyl (2-butyl-2-ethyl-1,3-propanediol) phosphite, Diisodecyl pentaerythritol diphosphite, distearyl pentaerythritol diphosphite, bis(2,4-di-tert.-butylphenyl)-pen-taerythritol diphosphite or tetraphenyl-dipropylene glycol diphosphite. Suitable light stabilizers are, for example, UV absorbers of the 2-hydroxyphenyl-benzotriazole type, those of the nitrogen-atom-substituted or unsubstituted HALS type, such as... B. Tinuvin® 292 or Tinuvin® 770 DF (BASF SE, Ludwigshafen, DE), or those described, for example, in "Lichtschutzmittel für Lacke" (A. Valet, Vincentz Verlag, Hannover, 1996) and "Stabilization of Polymeric Materials" (H. Zweifel, Springer Verlag, Berlin, 1997, Appendix 3, pp. 181-213). Other auxiliary and additive substances that may optionally be used in the process according to the invention are also the hydrazide group-containing and / or hydroxy-functional stabilizers described in EP-A 0 829 500, such as the addition product of hydrazine and propylene carbonate.The aforementioned auxiliary and additive substances can optionally be used individually or in any combination with one another in the process according to the invention in amounts of 0.001 to 3.0 wt.%, preferably 0.002 to 2.0 wt.%, particularly preferably 0.005 to 1.0 wt.%, in each case based on the total amount of polyisocyanate A). Regardless of the method of process, the manufacturing process yields completely clear and transparent polyisocyanates blocked with citric acid triesters (also citrates within the scope of the present invention) or organic solutions of such polyisocyanates, which exhibit significantly lower toxicity of the blocking agent, very high storage and solidification stability, and low viscosity. Furthermore, the use of one or more blocked polyisocyanates a), containing two or more 2-carbamoylpropane-1,2,3-tricarboxylate structures, is advantageous for reducing the 2024PF30029 - Abroad. - 14 -To increase the temperature at which curing begins and / or to improve the flexibility and / or sterilization resistance of one-component coatings for food containers, a further preferred embodiment of the present invention is described. The blocked polyisocyanates a) exhibit significantly lower viscosities compared to products known in the prior art, so that they can be used with a higher solids content in the one-component coating for food containers according to the invention. This results in the further advantage of an improved environmental footprint. The blocked polyisocyanates a) represent valuable starting materials for the production of the one-component coating for food containers according to the invention.They are ideally suited as crosslinking components for one-component, thermosetting, solvent-free, solvent-based, or aqueous coating systems, which are used particularly for the internal coating of food containers. Thus, the use of the one-component coating agent according to the invention as a thermosetting, solvent-free, solvent-based, or aqueous coating system, particularly in can coating and / or coil coating applications, and especially preferably for coating surfaces in contact with food, such as the internal coating of food containers, is a further object of the present invention. When used, the thermosetting preferably takes place by baking in temperature ranges of 90 to 210°C, more preferably from 105 to 180°C, more preferably from 110 to 160°C, and most preferably from 120 to 140°C.For the production of the one-component coating agent for food containers according to the invention, the blocked polyisocyanates a) are mixed with binders b), optionally with the addition of catalysts c) that accelerate the crosslinking reaction and optionally solvents and / or optionally auxiliary and additives d). The mixing must take place below the temperature at which the blocking agent is cleaved, since the release of the isocyanate groups would lead to premature crosslinking of the coating system. Preferably, the one-component coating agent for food containers according to the invention is produced at temperatures between 15 and 100°C. In the present context, the blocked polyisocyanates a) are also referred to as the blocked polyisocyanate component a) and / or the binders b) are also referred to as the binder component b).As a binder component b), the one-component coating agents according to the invention contain at least one binder reactive towards isocyanate groups with, on average, at least two isocyanate-reactive groups, such as hydroxyl, mercapto, amino or carboxylic acid groups, per molecule. 2024PF30029 - Foreign. - 15 -Preferably, these binders are (b) the usual di- and / or polyhydroxyl compounds known from polyurethane chemistry, such as polyester polyols, polyether polyols, polycarbonate polyols and / or polyacrylate polyols, or any mixtures of such polyols. Preferably, the binder (b) comprises or consists of polyester polyols, polyether polyols, polycarbonate polyols and / or polyacrylate polyols, or any mixtures of such polyols; more preferably, the binder (b) comprises or consists of polyester polyols and / or polyacrylate polyols.Suitable polyester polyols b) are, for example, those with a number-average molecular weight of 500 to 150,000 g / mol, calculable from functionality and hydroxyl number, preferably 600 to 30,000 g / mol, more preferably 700 to 15,000 g / mol, even more preferably 800 to 10,000 g / mol, particularly preferably 900 to 5,000 g / mol, and most preferably 1,000 to 3,000 g / mol, and / or with a hydroxyl group content of 0.03 to 21 wt.%, preferably 0.1 to 20 wt.%, particularly preferably 1 to 19 wt.%, and most particularly preferably 2 to 18 wt.%, as they are prepared in a manner known per se by reacting polyhydric alcohols with subtractive amounts of polyhydric carboxylic acids, corresponding carboxylic anhydrides, corresponding They can be produced from polycarboxylic acid esters of lower alcohols or by reaction with lactones.Preferably, higher NCO excesses are also possible at higher molecular weights mentioned above, as this further improves the properties of the available coatings for food containers.Suitable polyhydric alcohols for the production of polyester polyols (b) are, for example, 1,2-ethanediol, 1,2- and 1,3-propanediol, the isomeric butanediols, pentanediols, hexanediols, heptanediols and octanediols, 2-ethyl-2-butyl-1,3-propanediol, 2-ethyl-2-isobutyl-1,3-propanediol, 1,10-decanediol, 1,12-dodecanediol, 2,2,4,4-tetramethylcyclobutane-1,3-diol (TMCD), 1,2- and 1,4-cyclohexanediol, 1,4-cyclohexanedimethanol, 1,4-bis(2-hydroxyethoxy)benzene, 2,2-bis-(4-hydroxyphenyl)propane (bisphenol A), 2,2-bis-(4-hydroxycyclohexyl)propane (perhydrobisphenol), 1,2,3-propanetriol, 1,2,4-butanetriol, 1,1,1-trimethylolethane, 1,2,6-hexanetriol, 1,1,1-trimethylolpropane (TMP), bis-(2-hydroxyethyl)-hydroquinone, 1,2,4- and 1,3,5-trihydroxycyclohexane, 1,3,5-Tris(2-hydroxyethyl)-isocyanurate, 3(4),8(9)-bis-(hydroxymethyl)-tricyclo-[5.2.1.02,6]decane, di-trimethylolpropane, 2,2-bis(hydroxymethyl)-1,3-propanediol (pentaerythritol), 2,2,6,6-tetrakis(hydroxymethyl)-4-oxa-heptane-1,7-diol (dipentaerythritol), mannitol or sorbitol, low molecular weight ether alcohols such as diethylene glycol, triethylene glycol, tetraethylene glycol, dipropylene glycol or dibutylene glycol or low molecular weight ester alcohols such as hydroxypivalic acid neopentyl glycol esters, or mixtures of at least two such alcohols. 2024PF30029 - Foreign. - 16 -Suitable carboxylic acids or carboxylic acid derivatives for the production of the polyester polyols to be used in the one-component coating agents for food containers according to the invention (b) are polyhydric carboxylic acids, their carboxylic anhydrides, and polycarboxylic acid esters of lower alcohols. These are any aromatic, aliphatic, or cycloaliphatic, saturated or unsaturated di- and tricarboxylic acids or their anhydrides, in particular those with 4 to 18 carbon atoms, preferably with 4 to 10 carbon atoms, such as, for example,Succinic acid, succinic anhydride, glutaric acid, adipic acid, pimelic acid, cortic acid, azelaic acid, sebacic acid, decanedicarboxylic acid, maleic acid, maleic anhydride, fumaric acid, itaconic acid, itaconic anhydride, hexahydrophthalic acid, hexahydrophthalic anhydride, tetrahydrophthalic acid, phthalic anhydride, isophthalic acid, terephthalic acid, trimellitic acid, tetrahydrophthalic anhydride, dimethyl terephthalate, and bisglycol terephthalate, as well as dimeric and trimeric fatty acids, which can be used individually or in any mixture. If necessary, monocarboxylic acids, such as benzoic acid, acetic acid, propionic acid, butyric acid, or 2-ethylhexanoic acid, can also be used in minor quantities in the production of polyester polyols (b).Suitable polyester polyols b) for the one-component coating agents for food containers according to the invention are also those that can be produced in a manner known per se from lactones and polyhydric alcohols, such as those mentioned above as examples, as starter molecules via ring opening. Suitable lactones for the production of these polyester polyols b) are, for example, ^-propiolactone, ^-butyrolactone, ^- and ^-valerolactone, ^-caprolactone, 3,5,5- and 3,3,5-trimethylcaprolactone, or any mixtures of such lactones. The production of these lactone polyesters generally takes place in the presence of catalysts such as Lewis or Brønsted acids, organotin or titanium compounds at temperatures of 20 to 200°C, preferably 50 to 160°C.Suitable building blocks for the production of these polyester polyols b) include, for example, the polyhydric alcohols, polyhydric carboxylic acids, and their derivatives mentioned above as suitable for the production of polyester polyols b), which can also be used in the form of any mixtures. The production of the polyester polyols b) can be carried out according to methods known per se, such as those described in detail in E. Gubbels et al., Polyesters. In: Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH Verlag GmbH & Co. KGaA; 2018. URL:https: / / doi.org / 10.1002 / 14356007.a21_227.pub2. If necessary, catalytic amounts of common esterification catalysts, such as 2024PF30029 - Ausland. - 17 -For example, acids, bases, or transition metal compounds, such as titanium tetrabutylate, can be used. The esterification reaction is generally carried out in a temperature range of approximately 80 to 260°C, preferably 100 to 230°C, until the desired values ​​for hydroxyl and acid numbers are reached. Suitable polyether polyols b) are, for example, those with a medium molecular weight of 200 to 6000, preferably 250 to 4000, calculated from functionality and hydroxyl number, with a hydroxyl group content of 0.6 to 34 wt.%, preferably 1 to 27 wt.%, as can be obtained in a manner known per se by alkoxylation of suitable starter molecules. Any polyhydric alcohols, such as those described above as suitable for the preparation of polyester polyols b), can be used as starter molecules for the preparation of these polyether polyols.Suitable alkylene oxides for the alkoxylation reaction include, in particular, ethylene oxide and propylene oxide, which can be used in any order or in a mixture during the alkoxylation reaction. Suitable polycarbonate polyols (b) are, in particular, the reaction products of dihydric alcohols, such as those listed above as examples of polyhydric alcohols, with diaryl carbonates, such as diphenyl carbonate, dimethyl carbonate, or phosgene. Suitable polycarbonate polyols (b) also include those that contain ester groups in addition to carbonate structures. These are, in particular, the polyester carbonate diols known per se, such as those that can be obtained, for example, according to the teaching of DE-AS 1770245, by reacting dihydric alcohols with lactones, such as, in particular, β-caprolactone, and subsequently reacting the resulting polyester diols with diphenyl or dimethyl carbonate.Equally suitable polycarbonate polyols (b) are those that contain ether groups in addition to carbonate structures. These are in particular the polyether carbonate polyols known per se, such as those obtained, for example, by the process of EP-A 2046861 through the catalytic reaction of alkylene oxides (epoxides) and carbon dioxide in the presence of H-functional initiators. Suitable polyacrylate polyols (b) are, for example, those with a mean molecular weight of 800 to 50,000, preferably 1,000 to 20,000, calculated from functionality and hydroxyl number or determined by gel permeation chromatography (GPC), with a hydroxyl group content of 0.1 to 12 wt.%, preferably 1 to 10 wt.%, as they can be produced in a manner known per se by copolymerization of olefinically unsaturated monomers containing hydroxyl groups with hydroxyl-group-free olefinic monomers. 2024PF30029 - Foreign. - 18 -Examples of suitable monomers for the preparation of polyacrylate polyols b) are vinyl or vinylidene monomers such as styrene, ^-methylstyrene, o- or p-chlorostyrene, o-, m- or p-methylstyrene, p-tert-butylstyrene, acrylic acid, acrylonitrile, methacrylonitrile, acrylic and methacrylic acid esters of alcohols with up to 18 carbon atoms, such as... B. Methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate, n-butyl acrylate, isobutyl acrylate, tert-butyl acrylate, amyl acrylate, hexyl acrylate, 2-ethylhexyl acrylate, isooctyl acrylate, 3,3,5-trimethylhexyl acrylate, stearyl acrylate, lauryl acrylate, cyclopentyl acrylate, Cyclohexyl acrylate, 4-tert-butycyclohexyl acrylate, isobornyl acrylate, methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, isopropyl methacrylate, butyl methacrylate, isobutyl methacrylate, tert-butyl methacrylate, amyl methacrylate, hexyl methacrylate, 2-ethylhexyl methacrylate, Isooctyl methacrylate, 3,3,5-trimethylhexyl methacrylate, stearyl methacrylate, lauryl methacrylate, Cyclopentyl methacrylateCyclohexyl methacrylate, 4-tert-butylcyclohexyl methacrylate, norbornyl methacrylate or isobornyl methacrylate, diesters of fumaric acid, itaconic acid or maleic acid with alcohols having 4 to 8 carbon atoms, acrylamide, methacrylamide, vinyl esters of alkane monocarboxylic acids with 2 to 5 carbon atoms, such as vinyl acetate or vinyl propionate, hydroxyalkyl esters of acrylic acid or methacrylic acid with 2 to 5 carbon atoms in the hydroxyalkyl group, such as 2-hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl, 3-hydroxybutyl, 4-hydroxybutyl, trimethylolpropane monoacrylate or pentaerythritol monoacrylate or methacrylate,as well as any mixtures of such exemplary monomers. The one-component coating agents for food containers according to the invention may optionally contain catalysts c). These are in particular the urethanization catalysts already mentioned above as suitable for accelerating the reaction of the polyisocyanate component A) with the diol component B) and the amine component C), preferably bismuth(III), zinc(II), tin(II) and / or tin(IV) as the catalytically active metal ion and especially preferably bismuth(III) octoate, bismuth(III) triflate, bismuth(III) neodecanoate, zinc(II) chloride, zinc(II) n-octanoate, zinc(II) 2-ethyl-1-hexanoate, zinc(II) 2-ethylcaproate, zinc(II) stearate, zinc(II) naphthenate, zinc(II) acetylacetonate, tin(II) n-octanoate, tin(II) 2-ethyl-1-hexanoate, tin(II) ethylcaproate, tin(II) laurate, Tin(II) palmitate), tin(II) triflate, tin(II) chloride, dibutyltin(IV) oxide, dibutyltin(IV) dichloride, dibutyltin(IV) diacetate,Dibutyltin(IV) dimaleate, dibutyltin(IV) dilaurate and / or dioctyltin(IV) diacetate and, most preferably, bismuth(III) octoate, bismuth(III) triflate, bismuth(III) neodecanoate, zinc(II) n-octanoate, zinc(II) 2-ethyl-1-hexanoate and / or dibutyltin(IV) dilaurate. These catalysts c) occur in the one-component coating agents for food containers according to the invention as a single substance or in the form of any mixtures with each other in amounts of 0.001 wt.% to 6 wt.%, preferably from 0.002 wt.% to 5 wt.%, most preferably from 0.005 wt.% to 2 wt.% and entirely 2024PF30029 - Abroad, - 19 -Particularly preferably, the amount of 0.005 wt.% to 1 wt.%, calculated as the sum of all catalysts c) used and based on the total amount of solvent-free blocked polyisocyanate a) and solvent-free binder component b), is used. The one-component coating materials for food containers according to the invention may optionally also contain further auxiliary and additive substances d). In addition to the antioxidants and light stabilizers mentioned above, which may optionally be used in the process according to the invention, these include, for example, the usual plasticizers, leveling agents, rheology additives, slip additives, defoamers, fillers and / or pigments known to those skilled in the art, which are used in quantities customary in coating technology, if at all. A detailed overview of such suitable auxiliary and additive substances can be found, for example, in Bodo Müller, “Additive kompakt”, VincentzNetwork GmbH & Co KG (2009).In the production of the one-component coating materials for food containers according to the invention, the polyisocyanate component a) and the binder component b) are used or are present in such quantities that the equivalent ratio of the sum of blocked and unblocked isocyanate groups from a) to isocyanate-reactive groups from b) is from 1.5 : 1 to 12.0 : 1. Preferably, the polyisocyanate component a) and the binder component b) are present or are used in such quantities that the equivalent ratio of the sum of blocked and unblocked isocyanate groups from a) to isocyanate-reactive groups from b) is from 1.7 : 1 to 10.0 : 1, particularly preferably from 2.0 : 1 to 7.0 : 1, and most preferably from 2.5 : 1 to 5.0 : 1.The one-component coating materials for food containers according to the invention may optionally contain further compounds reactive towards isocyanate-reactive groups as an additional crosslinking component. These are, for example, compounds containing epoxy groups and / or aminoplast resins. Aminoplast resins are the condensation products of melamine and formaldehyde, or urea and formaldehyde, known in paint technology. All conventional melamine-formaldehyde condensates, either unetherified or etherified with saturated monoalcohols with 1 to 4 carbon atoms, are suitable. If further crosslinking components are used, the amount of binder with isocyanate-reactive groups must be adjusted accordingly. 2024PF30029 - Foreign. - 20 -The invention also relates to a method for producing a coating on and / or in a food container by reacting a one-component coating agent for food containers according to the invention under the influence of heat, preferably by baking in temperature ranges of 90 to 210°C, more preferably 105 to 180°C, particularly preferably 110 to 160°C, and most preferably 120°C to 140°C, or by reacting a one-component coating agent for food containers obtainable or produced according to the method under the influence of heat, preferably by baking in temperature ranges of 90 to 210°C, more preferably 105 to 180°C, more preferably 110 to 160°C, and most preferably 120°C to 140°C.A coated substrate comprising a hardened one-component coating agent for food containers according to the invention, or comprising a product obtainable or produced by the method for producing a coating on a substrate by reacting a one-component coating agent for food containers according to the invention under the influence of heat, preferably by baking in temperature ranges of 90 to 210°C, preferably 105 to 180°C, particularly preferably 110 to 160°C, and most preferably 120°C to 140°C, are further objects of the present invention, as is a substrate at least partially coated with at least one hardened one-component coating agent for food containers according to the invention, or at least partially coated with at least one hardened one-component coating agent for food containers, obtainable or produced according to the method according to the invention.The application of the inventive one-component coating agents for food containers can be carried out using methods known per se, for example by spraying, brushing, dipping, flooding, or with the aid of rollers or doctor blades in one or more layers. Any substrates are suitable, such as metal, wood, glass, stone, ceramic materials, composites, or plastics of all kinds, which may optionally be provided with conventional, known primers, fillers, base coats, and / or clear coats prior to coating. The curing of the dried films is carried out by baking at temperatures ranging from 90 to 210°C, preferably 105 to 180°C, particularly preferably 110 to 160°C, and most preferably 120 to 140°C. The dry film thickness can be, for example, 10 to 120 µm. 2024PF30029 - Foreign. - 21 -The one-component coating agents for food containers according to the invention can also be used for continuous strip coating, whereby maximum curing temperatures, known to those skilled in the art as peak metal temperatures, between 130 and 300°C, preferably 190 to 260°C, and / or dry film thicknesses of, for example, 3 to 40 µm can be achieved. Such use is a further object of the present invention. The features and embodiments characterized as exemplary and preferred for the blocked polyisocyanate a) are also preferred for the further objects of the invention. The following examples serve to clarify the present invention but should in no way be understood as limiting the scope of protection.

[0002] 2024PF30029 - Abroad - 22 -Examples of syntheses were carried out inertly, using the Schlenk technique, in previously baked-out glass apparatus under dry nitrogen. All percentages refer to weight unless otherwise stated. The determination of NCO content, including the content of free NCO groups, was performed titrimetrically according to DIN EN ISO 11909:2007-05. The course of the blocking reaction and the NCO-free status of the blocked polyisocyanates were assessed by the decrease or absence of the isocyanate band (approx. 2270 cm⁻¹). -1 The residual monomer content was measured using gas chromatography with an internal standard according to DIN EN ISO 10283:2007-11. All viscosity measurements were performed with a Physica MCR 51 rheometer from Anton Paar Germany GmbH (DE) according to DIN EN ISO 3219:1994-10 at a shear rate of 250 s⁻¹. -1Chemicals and starting materials: Triethyl citrate (Merck KGaA, Sigma Aldrich Germany) ^-Caprolactam (hereinafter also abbreviated as "E-CAP") (Merck KGaA, Sigma Aldrich Germany) Hexamethylene diisocyanate HDI (Desmodur ® H, Covestro Deutschland AG)Desmodur® BL 2078 / 2 (^-Caprolactam blocked IPDI polyisocyanate, Covestro Deutschland AG) Desmorapid ®SO (Tin Octoate, Covestro Deutschland AG) Butyl Acetate (Azelis Deutschland GmbH) Solvent Naphtha 150 ND (S 150 ND) (DHC Solvent Chemie GmbH, Germany) Bismuth Neodecanoate (Merck KGaA, Sigma Aldrich Germany) Uralac® SH979 (saturated polyester with an average molecular weight of 11000Da, OH number approx. 7.5 mg KOH / g, Covestro Coating Resins BV Netherlands) Kronos 2310 (TiO2 white pigment, Kronos Worldwide, Inc. USA) Resiflow FL 2 (silicone-free surface additive, Worlée-Chemie GmbH, Germany) Application-related tests: Flexibility and elasticity tests Erichsen cupping test performed according to DIN EN ISO 20482: The Erichsen flexibility test evaluates the flexibility of a coating based on a slow deformation. By slowly pulling a cup from a coated sheet (70 mm x 150 mm x 0.24 mm), one obtains an indication of how the 2024PF30029 - Abroad behaves. - 23 -The behavior of coatings during forming processes in practice. In a first step, Erichsen cup 1 was produced by punching out a round sheet metal blank (diameter 64 mm) and then slowly (10 s) forming it into a cup approximately 25 mm long. This cup was then slowly (10 s) stretched into Erichsen cup 2 with a length of 33 mm. After the plates had aged for at least 5 days at room temperature, the Erichsen cups were formed. Sterilization test after forming: Formed cans or cups were placed in an autoclave, which was then filled with water. The autoclave was closed and heated to 130°C. Once 130°C was reached, this temperature was maintained for 60 minutes. After cooling to approximately...At 70°C, the autoclave was opened and the cans or cups were removed, dried, and assessed according to the following scale: The Erichsen cups were assessed according to the following scale: 1 very poor = complete delamination; 2 poor = delamination to the rim; 3 moderate = half of the cup is delaminated; 4 good = slight delamination only at the edges, max. 2 mm; 5 very good = no coating defects. The assessment was carried out before and after sterilization. Wedge Bend Test performed according to ASTM D 3281: To determine the formability of coated sheets, the Wedge Bend Test is used, which was performed after the sheets had been aged at room temperature for at least 5 days. A sheet (120 mm x 30 mm) was bent over a 6 mm thick cylindrical mandrel.The folded plate produced in this way was then clamped in an impact bending tester (Erichsen model 471) to form a wedge-shaped contour, flat at one end and 6 mm in diameter at the other. This test piece was then immersed in a 3% hydrochloric acid copper sulfate solution for 4 minutes. Any cracks that may have formed in the coating are discolored by this process. The width of the uncracked surface in centimeters was measured from the 6 mm side. The larger the number, the better the wedge bending result. 2024PF30029 - Foreign. - 24 -Chemical resistance to typical food ingredients under sterilization conditions: Coated test panels were placed vertically in a glass container, which was half-filled with the test liquid (food simulant). The glass container was sealed and placed in an autoclave. The autoclave was sealed and heated to 130°C. Once 130°C was reached, this temperature was maintained for 60 minutes. After cooling to approximately 70°C, the autoclave was opened, the panels were removed, rinsed with tap water, and dried with absorbent paper towels. The coatings were visually assessed for the gas phase (top of the panel) and the liquid phase (bottom half of the panel).Examples of food simulants are: 1) tap water 2) 2% citric acid in water 3) 2% lactic acid in water 4) 3% acetic acid in water. The coatings were then assessed according to the following scale: Roughness 1 = complete delamination of the coating 10 = no roughness at all. Blush 1 = completely discolored due to water absorption; 10 = no discoloration at all; Adhesion (using adhesive tape test): 1 = complete delamination; 10 = no delamination at all; 2024PF30029 - Abroad - 25 -Starting polyisocyanate: Polyisocyanate containing 1:isocyanurate groups, based on HDI, prepared according to EP 330 966. 1000 g of hexamethylene diisocyanate (HDI) were placed in a four-necked flask equipped with a stirrer, reflux condenser, nitrogen feed tube, and internal thermometer. The flask was degassed three times at room temperature by applying a vacuum of approximately 50 mbar and then purged with nitrogen. Subsequently, to initiate the trimerization reaction, 12 g of a catalyst solution, 0.5% (2-hydroxyethyl)trimethylammonium hydroxide in a 1:1 mixture of methanol and 2-ethylhexane-1,3-diol, was added dropwise over 30 minutes and slowly heated to 70°C. The mixture heated to approximately 75°C and was stirred at this temperature for one hour. Then, another 12 g of catalyst solution were added dropwise and the reaction mixture was stirred until an NCO content of 38.0% was reached.The reaction was stopped equimolarly (based on catalyst loading) with dibutyl phosphate (25% in HDI) and subsequently freed of excess HDI by thin-film distillation (130 °C, 0.1 mbar). A colorless polyisocyanurate polyisocyanate with the following properties was obtained: NCO content: 21.7 wt%; Monomeric HDI content: < 0.1%; Solids content: 100%; Viscosity (23 °C): 3000 mPas. Blocked Polyisocyanates: Blocked Polyisocyanate 1: Polyisocyanate 1 (986.4 g, 1.0 val) was dissolved in butyl acetate (800.3 g). Triethyl citrate (1414.6 g, 1.0 val) was added dropwise to this solution under dry nitrogen and mechanical stirring. The reaction mixture was then heated to 50 °C with desmorapide. ®SO₂ (100 ppm) was added and stirred until all NCO groups had reacted (determined by IR spectroscopy). A colorless, blocked polyisocyanate was obtained with the following properties: Free NCO content: 0.0% Blocked NCO content: 6.7% Solids content: 75% 2024PF30029 - Abroad - 26 -Viscosity (23°C): 1180 mPas Blocked polyisocyanate 2: Desmodur® BL 2078 / 2, a ^-caprolactam (hereinafter also abbreviated as “E-CAP”) blocked IPDI polyisocyanate Blocked NCO content: 7.2% Solids content: 60% Viscosity (23°C): 1750 mPas One-component coating agent for food containers (1K-PUR systems) General manufacturing procedure: Polyester (Uralac® SH979), TiO2 white pigment (Kronos 2310) and solvent naphtha were weighed together and homogenized using a spatula. Subsequently, 200 g of glass beads (3 mm diameter) were added, and the mixture was milled using a dissolver (Dispermill® Orange-line, equipped with a 41 mm dissolver disc) for 20 minutes at 2000 rpm and a further 10 minutes at 1000 rpm. After filtering off the glass beads, a pigment paste was obtained. This pigment paste was then mixed with a further quantity of polyester (Uralac® SH979) and blocked polyisocyanate (NCO to OH ratio 4).26 to 1), catalyst (Bismuth neodecanoate 20% in Solvent Naphtpha) and flow additive (Resiflow FL 2.10% in MPA, 0.1% on solid resin) mixed and adjusted with Solvent Naphtpha to a solids content of approximately 46.3%. Examples 1 to 6 and their exact composition are shown in the following tables: Table 1: Formulation of 1K-PUR systems 1 and 2. Example 1 (according to the invention) 2 (comparison) Blocking agent TEC E-CAP Kronos 2310 189.74 g 190.07 g Uralac SH979 481.88 g 506.26 g Solvent Naphtha 245.26 g 219.95 g Blocked polyisocyanate 1 72.28 g Blocked polyisocyanate 2 72.86 g Bismuth neodecanoate (20% in SN) 8.13 g 8.15 g Resiflow FL 2 (10% in MPA) 2.71 g 2.72 g Solids content (%) 46.3 46.4 NCO / OH ratio 4.26 / 1.00 4.26 / 1.00 Catalyst content (%) 0.6 0.62024PF30029 - Abroad. - 27 -Table 2: Formulation of 1K-PUR systems 3 and 4. Example 3 (according to the invention) 4 (comparison) Blocking agent TEC E-CAP Kronos 2310 189.23 g 189.56 g Uralac SH979 480.57 g 504.88 g Solvent Naphtha 244.6 g 219.35 g Blocked polyisocyanate 1 72.09 g Blocked polyisocyanate 2 72.66 g Bismuth neodecanoate (20% in SN) 10.81 g 10.83 g Resiflow FL 2 (10% in MPA) 2.70 g 2.71 g Solids content (%) 46.3 46.4 NCO / OH ratio 4.26 / 1.00 4.26 / 1.00 Catalyst content (%) 0.8 0.8 Table 3: Formulation of 1K-PUR systems 5 and 6. Example 5 (according to the invention) 6 (comparison) Blocking agent TEC E-CAP Kronos 2310 188.21 g 188.54 g Uralac SH979 477.99 g 506.26 g Solvent Naphtha 243.28 g 219.95 g Blocked polyisocyanate 1 71.70 g Blocked polyisocyanate 2 72.27 g Bismuth neodecanoate (20% in SN) 16.13 g 16.16 g Resiflow FL 2 (10% in MPA) 2.69 g 2.69 g Solids content (%) 46.3 46.4 NCO / OH ratio 4.26 / 1.00 4.26 / 1.00 Catalyst content (%) 1.2 1.2

[0003] 2024PF30029 - Abroad- 28 - Application testing: The above-mentioned one-component coatings were applied to electrolytically tinned tinplate using a doctor blade with a dry film thickness of approximately 15–20 g / m² and oven-cured. The curing conditions and the resulting application tests are summarized in the following tables: Table 4: Testing of the chemical resistance (MEK double strokes) and flexibility (Wedgebend, Erichsen) of the coatings. 2024PF30029 - Abroad - 29 - t e E mp E n i n 1 b 151 e i 2 r 61 12 1 11 12 r a b e n 00708000 5060708000 t u r e mrn n i nd ( ° n C-aue) r B e 6 42 2 2 53 1 11 is p e i l B o l ( V T ce EE k i r e g e -l C C r u A ( e n i c h P r gs ) f .) m i t te l * B K a is m 1 0 t a u . t 2 . 80 .60 .60 .61 .20 .80 .60 .60 .6 ( % ly s h ) a N t o e r * ode c a 1 1 11 D h M no 334 9 30 60000 50 ü op a / 10 / 10 / 10 / 3b E epeK t e - l W 8 7 8 88 88 ( ed 6 6 % g 41252 4789 83 o e k b ) end C 5 55 5 5 55 55 5 u B p 1 Eew r ic e h r t u C s e n 555 5 5 u ng 5 5 55 5 p : 5 2 = b e Ws t a e C s s, 15555 5 55 55 5 u s p n e a= 1 c r h ( s S E s t e ch r i r e t l e c i lc r h . s ) 6h i i l s e 0 t e C a n m s te 5555 5 55 55 5 u t io n n i sp 2130 ° C 2024PF30029 - Abroad - 30 - Table 5: Testing of resistance to food stimulants under sterilization conditions. 2024PF30029 - Abroad - 31 - t e m E n i E 15161 12 1 11 1 2 ( ° pb n i 007080005060708000 C e) r a r e 1 bt u nn 2 m r e nr - n i nda 4 2 22 5 31 1 1 B u 6 s p ee i e r l - in 6eod * ( B o 0 Se B V c s a i and E l m r g e - ( e T m c m t k n i e r l C A rf EC it t ie e i r / i l s now i P .) l u n13 a etc. t h c h t i t e ) gs 0 o - ° C n 1 2 0 8 0 6 0 60 K . . . . . 61 .20 .80 .60 .60 .6 ( % a) t . * 8 101010101010101010 LR and L ueh it u 7 10101010101010101010 G and i ng s L w = 22 9 1 F 0108 10101010 LB as l u l s ü s 47 101010111 1 1 G s eh r s i 00000 gph 1010111791 1 1 L R a 000 000 a C s e u i , G 8101010101010101 h t ro 0 10 G e t i ne 2 = n % G 23 6 78 3 67 8 8 L B s a ä u p l u s 1 11 1 r e h 570000 10101010 G s h a s e 1 R / / 084 45 2 34 5 5 L a B u 1 1 11 1 11 1 h ew 800000000 10 G e 2 e t i % rt u 11235 2 34 5 5 L B M ng : 11 1 1 u l s i c l h 13 5 800 8 900 10 G h s 0 ä = 11 1 H u b 000 89 6 56 8 8 L r e e a s t f t e 101010111 11 1 1 G u n s 0000000 g ,1 = 8108 87 7 77 7 7 L R s a c u h 11 1 11 11 h e l 00000 900 1010 G e 3 c t i h % t e 125 77 7 77 7 7 L B E s te1 G u l ss 36 9 99 80 9 9 9 s h s ig s 9 9 101010101010101 a 0 LH etc r e 1 1 1 11 1 1 ft u 0000000 101010 G ng 1 1 1 11 1 1 S 29507176805761 97 1 1 47979 um2024PF30029 - abroad - 32 - Table 6: Testing of resistance under basic sterilization conditions. c h E e l t e E n i cm n 1 bh i t e 1 2 r 5 1 e s t 06 1 07 1 2 1 1 1 1 2 ( 08000 5060708000 ° C peb r e m nn e ) r a n n i ds t u nar - ue r B e 6 4 2 2 2 531 1 1 s i pe i l S * t e B ( i e B s m r o r l i i l s( f in c a u V t h e E d k F a t io n r u g - C n T e i l n E r u t 6e e l A gC n P od i a 0 c P s g g n m e h e c ) m s m el a ä it n t i 1 n ß e l 3 o ) 0 a t e ° C K a 1 00 t a L= . 2 . 8 . 60 .60 .61 .20 .80 .60 .60 .6 ( % l ) y sa F t o ü l r * s s ig 81 1 1 1 1 1 1 1 1 R p 0000 00000 L a L h u e a h it s e 7 10101010 1010101010 G e u n , t i g G 1 1 1 1 1 1 s w = 22 900 80000 L B a G u l s a s p 4 700 10 1010101010 G s s 1 1 h er ha s e 1010 999 9 1 0 7 7 8 0 L R . 1 / a % / B uh D ew e 9 9 101010 1 1 1 1 1 G t i m i e 00000 e r tu t h n y l g e :122 4 7 9 678 8 9 L B t h a 0= u l no b s 1 1 1 1 h a l e 5 5 7 90 1 1 G m s 00000 t e n i s, 1S = 4452687 u 6 79 7376777779 m m e2024PF30029 - Ausland - 33 -Table 4 shows that the 1K-PUR formulations 1, 3, and 5 according to the invention, based on citrate-blocked polyisocyanates, exhibit excellent to good solvent resistance to MEK over the entire tested temperature range. 1K-PUR formulations based on E-CAP-blocked polyisocyanates provide sufficient MEK resistance only at 200°C (Comparative Example 2, 200°C). At lower temperatures, see Comparative Examples 2 at 180°C and 170°C, as well as Comparative Example 4 at 160°C and Comparative Example 6 at 150°C, inadequate MEK resistance is achieved. The flexibility after slow deformation (Erichsen test) is excellent for all formulations, both before and after sterilization. The elasticity and flexural properties were investigated in the wedge bend test. The paints exhibit very similar elasticity properties at baking temperatures of 200 to 180°C.At a curing temperature of 170°C, initial advantages of the system 1 according to the invention compared to comparison 2 are already evident. These advantages become even more pronounced at lower temperatures. Coatings based on examples 3 and 5 according to the invention only show initial small cracks at 87% and 84% bending, respectively, whereas coatings based on comparison examples 4 and 6 begin to crack at 61% and 64% bending. Table 5 shows that the coating 1 according to the invention exhibits a similarly high resistance to typical food simulants at a curing temperature of 200°C as coatings based on comparison example 2. At lower curing temperatures, however, the advantage of the formulations 1, 3, and 5 according to the invention becomes clearly apparent.Even at 180°C, slight advantages are apparent (see Example 1 and Comparative Example 2 at 180°C), which become even more pronounced at lower temperatures (see Example 5 and Comparative Example 6). A similar picture emerges under alkaline sterilization conditions (Table 6). The resistances of the E-CAP-based 1-component PUR systems (Comparative Examples 2, 4, and 6) are already significantly below the level of the citrate-blocked one-component coatings 1, 3, and 5 according to the invention, even at a curing temperature of 170°C. In summary, the citrate-blocked polyisocyanates according to the invention are ideally suited as crosslinking components in one-component coatings for food containers, which provide highly resistant, flexible, and elastic coatings even under sterilization conditions and low curing temperatures.

Claims

2024PF30029 - Abroad - 34 -Claims 1. A one-component coating agent for food containers, comprising a) at least one blocked polyisocyanate containing two or more 2-carbamoylpropane-1,2,3-tricarboxylate structures, b) at least one binder reactive towards isocyanate groups with, on average, at least two isocyanate-reactive groups per molecule, c) optionally catalysts, and d) optionally solvents and / or optionally excipients and additives, wherein a) and b) are present in an equivalent ratio of the sum of blocked and unblocked isocyanate groups from a) to isocyanate-reactive groups from b) of 1.5 : 1 to 12.0 :

1.

2. The coating composition according to claim 1, characterized in that the blocked polyisocyanate a) additionally contains one or more isocyanurate, allophane, urethane, urea, uretdione, iminooxadiazindione, oxadiazintrione and / or biuret structures.3.The coating composition according to one of claims 1 or 2, characterized in that the two or more 2-carbamoylpropane-1,2,3-tricarboxylate structures of the blocked polyisocyanate a) have a general formula (I). exhibit, in which R independently represents any saturated or unsaturated, linear or branched, aliphatic residue with 1 to 18 carbon atoms, saturated or unsaturated cycloaliphatic residue with 3 to 18 carbon atoms, araliphatic residue with 7 to 18 carbon atoms and / or aromatic residue with 6 to 18 carbon atoms, each being substituted or unsubstituted and / or containing heteroatoms in the chain. 2024PF30029 - Foreign - 35 - 4. The coating composition according to one of claims 1 to 3, characterized in that the two or more 2-carbamoylpropane-1,2,3-tricarboxylate structures of the blocked polyisocyanate a) a general formula (I), (I) having, in which R independently represents any saturated or unsaturated, linear or branched aliphatic residue with 1 to 8 carbon atoms and / or saturated or unsaturated cycloaliphatic residue with 5 to 8 carbon atoms, each being substituted or unsubstituted and / or having heteroatoms in the chain, preferably in which R independently represents any saturated or unsaturated, linear or branched aliphatic residue with 1 to 4 carbon atoms, each being substituted or unsubstituted and / or having heteroatoms in the chain, particularly preferably in which R independently represents any saturated or unsaturated, linear or branched aliphatic residue with 2 to 4 carbon atoms.5.The coating composition according to any one of claims 1 to 4, characterized in that, for the production of the blocked polyisocyanate component, a) polyisocyanates are used which have an isocyanate group content of 6.0 to 26.0 wt.%, preferably 8.0 to 25.0 wt.%, particularly preferably 10.0 to 24.0 wt.%, and / or a monomeric diisocyanate content of less than 0.50 wt.%, preferably less than 0.30 wt.%, more preferably less than 0.20 wt.%, particularly preferably less than 0.10 wt.%.

6. The coating composition according to any one of claims 1 to 5, characterized in that the binder b) comprises or consists of polyester polyols, polyether polyols, polycarbonate polyols and / or polyacrylate polyols or any mixtures of such polyols, preferably comprising or consisting of polyester polyols and / or polyacrylate polyols. 7.The coating composition according to any one of claims 1 to 6, characterized in that a) and b) are present in an equivalent ratio of the sum of blocked and unblocked isocyanate groups from a) to isocyanate-reactive groups from b) of 1.7 : 1 to 10.0 : 1, particularly preferably of 2.0 : 1 to 7.0 : 1, most preferably of 2.5 : 1 to 5.0 :

1. 2024PF30029 - Foreign. - 36 -8. The coating composition according to any one of claims 1 to 7, characterized in that it comprises one or more catalysts c) in amounts of 0.001 wt.% to 6 wt.%, preferably 0.002 wt.% to 5 wt.%, particularly preferably 0.005 wt.% to 2 wt.% and most preferably 0.005 wt.% to 1 wt.%, calculated as the sum of all catalysts c) used and based on the total amount of solvent-free blocked polyisocyanate a) and solvent-free binder component b).

9. Method for producing a shaped body or an adhesive between two substrates or a coating on a substrate by reacting a one-component coating agent for food containers according to one of claims 1 to 8 under the influence of heat, preferably by baking in temperature ranges of 90 to 210°C, preferably 110 to 160°C, particularly preferably 120 to 140°C.10.

11. Use of the one-component coating agent for food containers according to any one of claims 1 to 8 as thermosetting solvent-free, solvent-based, or aqueous coating systems, preferably thermosetting by baking in temperature ranges of 90 to 210°C, more preferably 110 to 160°C, particularly preferably 120 to 140°C.

12. Use of the one-component coating agent for food containers according to any one of claims 1 to 8 in coil coating applications at peak metal temperatures between 130 and 300°C, more preferably 190 to 260°C.

13. Molded body or bonded substrate comprising a cured one-component coating agent according to any one of claims 1 to 8 or comprising a product obtainable or produced by the method according to claim 9. 14.Substrate, at least partially coated with at least one hardened one-component coating material according to one of claims 1 to 8 or at least partially coated with at least one hardened one-component coating material, available or produced according to the method according to claim 9.

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