Process for preparing tertiary araliphatic carbodiimides

Abstract

The invention relates to: a process for preparing tertiary araliphatic carbodiimides from araliphatic isocyanates by reaction in the presence of one or more diazaphospholidine oxides; to mixtures obtainable by the method, comprising araliphatic carbodiimides and diazaphospholidine oxides; and to the use thereof as hydrolysis stabilizers in PU and TPU.

Description

[0001] Method for the production of tertiary araliphatic carbodiimides

[0002] The present invention relates to the field of carbodiimides, their production and use as hydrolysis inhibitors in polyurethane (PU) and thermoplastic polyurethane (TPU).

[0003] Sterically hindered carbodiimides have proven effective in many applications, e.g., as hydrolysis inhibitors for thermoplastic polymers, ester-based polyols, polyurethanes, triglycerides, and lubricating oils, etc. In polyurethanes, in particular, sterically hindered carbodiimides achieve a significantly higher hydrolysis protection effect compared to less sterically hindered carbodiimides.

[0004] According to the state of the art, carbodiimides are synthesized from isocyanates, which are (poly)condensed (carbodiimidized) by basic or heterocyclic catalysis with the elimination of CC>2. Mono- or polyfunctional isocyanates can be converted to monomeric or polymeric carbodiimides.

[0005] The catalysts commonly used are alkali or alkaline earth compounds. Phosphorus-containing catalysts for the synthesis of aliphatic and aromatic carbodiimides are described in FR1469946. However, these are not suitable for the preparation of sterically hindered carbodiimides, so phosphorus oxides, especially 1-methyl-2-phospholene-1-oxide (MPO), have become the preferred choice.

[0006] The phosphorus-containing catalysts from the prior art have the disadvantage of interfering in most PU applications even at very low concentrations (ppm), as they lead to undesirable side reactions.

[0007] The complete removal of these phosphorus-containing catalysts is technically very expensive and is usually carried out by elaborate distillation steps such as those described in EP2897934.

[0008] Other basic and / or heterogeneous alternative catalysts from the prior art, as described in WO2015185645, WO 2016202781 or WO 2022219110, usually show significantly lower activity and are also only suitable for production scale with additional costly process steps for separating or decomposing / removing the residual catalysts after the reaction for the production of carbodiimides for use in PU applications.

[0009] The object of the present invention was therefore to provide an improved process which enables the production of sterically hindered carbodiimides in high yields and uses a catalyst that does not interfere with the polymerization of PU, so that the sterically hindered carbodiimides obtained can be used in the production of hydrolysis-stabilized polyurethanes, in particular TPU, without significant removal of the catalyst.

[0010] Surprisingly, it has now been found that the aforementioned problems are solved by a process for the preparation of tertiary araliphatic carbodiimides from araliphatic isocyanates, wherein the araliphatic isocyanates are reacted in the presence of one or more diazaphospholidine oxides of formula (III), in which R 1 , R 2 , R 3 are independently selected from Ci-Ce-alkyl, cyclohexyl and aryl and wherein preferably R1 , R 2 , R 3 Methyl are.

[0011] The term tertiary araliphatic carbodiimides refers to compounds in which one or both, preferably both, sides of the carbodiimide function are bonded to a tertiary carbon atom bearing two alkyl groups and one (possibly substituted) aryl group. These carbodiimides exhibit a high degree of steric shielding of the carbodiimide function.

[0012] The araliphatic isocyanates used to produce the tertiary araliphatic carbodiimides are obvious to a person skilled in the art to derive from the structure of the carbodiimides.

[0013] A preferred embodiment of the invention is a method for the preparation of tertiary araliphatic carbodiimides of formula (1a) or the formula (Ib) wherein n corresponds to a number from 0 to 20, preferably 0 or 3 to 8, most preferably 0 or 4 to 5,

[0014] I corresponds to a number from 1 to 20, preferably from 3 to 8, most preferably from 4 to 5,

[0015] R 1 Independently selected from compounds of the formula laa, lab, lac or lad, compounds of the formula lab are preferred.

[0016] R 4 and R 5 Independently selected from Ci - C lkyl are the residues R 6 and R 7 are independently selected from Ci-C4-alkyl, Ci-C4-alkoxy, a, b, c represents a number from 0 to 4, preferably 0,

[0017] R 2 and R 3 are independently selected from -O-(Ci - C2o-Alkyl), -O-(Ci - C20- Alkenyl), -O-(Cs - C2o-Cycloalkyl), -O-Aryl, -O-(C? - C2o-Alkyaryl), -O-[(CH2)kO] g -R 8 , with k= 1-3, g = 0-12 and R 8 = H or Ci-C4-alkyl.

[0018] A further preferred embodiment of the invention is a process for the preparation of tertiary araliphatic carbodiimides selected from bis[3-isopropenyl-α,α-dimethylbenzyl]carbodiimide Ha and compounds of formula 11 b wherein

[0019] I corresponds to a number from 1 to 20, preferably from 3 to 8, most preferably from 4 to 5, and m corresponds to a number from 1 to 20, preferably from 3 to 15, most preferably from 5 to 11.

[0020] Another preferred embodiment of the invention relates to a process for the production of tertiary araliphatic carbodiimides wherein 3-isopropenephenyl-a,a-dimethylbenzyl isocyanate (Illa) and / or m-tetramethylxylene diisocyanate (111b) are used as araliphatic isocyanates.

[0021] In the process according to the invention for the production of tertiary araliphatic carbodiimides, the conversion of isocyanates to carbodiimides usually takes place at temperatures of 160 to 220°C, preferably 180 to 200°C, particularly preferably 180 to 190°C.

[0022] In a preferred embodiment, the reaction takes place at a pressure of 10–1000 mbar, preferably 20–300 mbar, and particularly preferably 50–100 mbar. The reaction can be carried out in the presence or absence of a nitrogen stream.

[0023] Suitable diazaphospholidine oxides of formula III are compounds in which R 1 , R 2 , R 3 are independently selected from Ci-Ce-alkyl, cyclohexyl and aryl, preferably Ci-C3-alkyl, cyclohexyl and phenyl and particularly preferably 1,2,3-trimethyl-2-oxo-1,3,2-diazaphospholidine)

[0024] In a preferred embodiment, the diazaphospholidine oxides are used in a concentration of 0.5 to 2 wt.%, preferably 0.8 to 1.5 wt.% and particularly preferably 1 to 1.2 wt.%, each based on the total amount of araliphatic isocyanates.

[0025] Carbodiimidation can be carried out in the substance or in a solvent. Preferably, alkylbenzenes, paraffin oils, polyethylene glycol dimethyl ethers, ketones, or lactones are used as solvents.

[0026] In one embodiment of the invention for the production of end-functionalized carbodiimides, the terminal free isocyanate groups of the carbodiimides are reacted with aliphatic and / or aromatic alcohols and / or alkoxypolyoxyalkylene alcohols following the carbodiimidation. To produce the carbodiimides of formula 1a and 1b according to the invention, the carbodiimidation is typically stopped when the reaction mixture has the desired content of NCO groups, corresponding to an average degree of condensation of 1. In one embodiment of the present invention, the temperature of the reaction mixture is reduced to 50–120 °C, preferably 60–100 °C, and particularly preferably to 80–90 °C, and the terminal free isocyanate groups of the carbodiimides are end-functionalized.

[0027] Preferably, the free terminal isocyanate groups of the carbodiimides are reacted with aliphatic and / or aromatic alcohols and / or alkoxypolyoxyalkylene alcohols, preferably in a slight excess of -OH groups, optionally in the presence of a PU catalyst known to those skilled in the art, preferably tert-amines or organotin compounds, particularly preferably DBTL (dibutyltin dilaurate) or DOTL (dioctyltin dilaurate). The stoichiometric ratio of alcohols and / or alkoxypolyoxyalkylene alcohols to carbodiimides is preferably 1.005–1.05:1, particularly preferably 1.01–1.03:1, based on the N=C=O groups present.

[0028] To prepare the carbodiimides of forms Ib with n > 0 according to the invention, 3-isopropenyphenyl-a,a-dimethylbenzyl isocyanate (Illa) and m-tetramethylxylene diisocyanate (Illbb) are preferably presented in a suitable ratio and subsequently carbodiimidated in the presence of the catalyst of formula III.

[0029] A further object of the invention is mixtures containing tertiary araliphatic carbodiimides and, based on the araliphatic carbodiimides, diazaphospholidine oxides of formula (III) in amounts of 0.5 to 2 wt.%, preferably 0.8 to 1.5 wt.%, particularly preferably 1 to 1.2 wt.%, which are obtainable by the processes according to the invention for the production of tertiary araliphatic carbodiimides in the embodiments described above. These mixtures can be advantageously used for the production of hydrolysis-stabilized polyurethane (PU), preferably hydrolysis-stabilized thermoplastic polyurethane (TPU). This use thus constitutes a further object of the invention.

[0030] A further object of the present invention is a process for the production of polyurethanes (PU), preferably thermoplastic polyurethanes, characterized in that polyols, preferably polyester polyols, are reacted with polyisocyanates, optionally in the presence of PU catalysts and auxiliary and / or additives, in the presence of the carbodiimide according to the invention, to form polyurethanes. The production of the polyurethanes is preferably carried out as described in WO 2005 / 111136 A1.

[0031] Polyurethanes are formed almost quantitatively by the polyaddition reaction of polyisocyanates with polyhydric alcohols, the polyols. The linkage occurs through the reaction of an isocyanate group (-N=C=O) of one molecule with a hydroxyl group (-OH) of another molecule to form a urethane group (-NH-CO-O-).

[0032] The reaction pathway between diisocyanate and polyol depends on the molar ratio of the components. Intermediates with the desired average molecular weight and desired end groups can be obtained. These intermediates can then be reacted (chain-extended) with a diol or diamine at a later stage, forming the desired polyurethane or polyurethane-polyurea hybrid. These intermediates are generally referred to as prepolymers.

[0033] Suitable polyols for the production of prepolymers are polyalkylene glycol ethers, polyether esters or polyesters with terminal hydroxyl groups (polyester polyols).

[0034] The polyols according to the invention are compounds which preferably have a molecular weight in (g / mol) of up to 2000, preferably in the range of 500 to 2000 and particularly preferably in the range of 500 to 1000.

[0035] The term polyol, as used in this invention, includes diols, triols, and compounds with more than three hydroxyl groups per molecule. The use of triols is particularly preferred.

[0036] Preferred polyols are polyester polyols and / or polyether ester polyols.

[0037] It is advantageous if the polyol has an OH number of up to 200, preferably between 20 and 150 and particularly preferably between 50 and 115.

[0038] Polyester polyols that are reaction products of various polyols with aromatic or aliphatic dicarboxylic acids and / or polymers of lactones are particularly suitable.

[0039] Aromatic dicarboxylic acids that can be used to form suitable polyester polyols are preferred. Terephthalic acid, isophthalic acid, phthalic acid, phthalic anhydride, and substituted dicarboxylic acid compounds with a benzene ring are particularly preferred. Aliphatic dicarboxylic acids that can be used to form suitable polyester polyols are preferred, especially sebacic acid, adipic acid, and glutaric acid.

[0040] Polymers of lactones are preferred if they can be used to form suitable polyester polyols, especially polycaprolactone.

[0041] Both the dicarboxylic acids and the polymers of lactones are commercially available substances.

[0042] Particularly preferred are polyols which can be used to form suitable polyester polyols, especially ethylene glycol, butanediol, neopentyl glycol, hexanediol, propylene glycol, dipropylene glycol, diethylene glycol and cyclohexanedimethanol.

[0043] In another preferred embodiment of the invention, the polyols are polyether ester polyols.

[0044] For this purpose, the reaction products of various previously mentioned polyols with aromatic or aliphatic dicarboxylic acids and / or polymers of lactones (e.g. polycaprolactone) are preferred.

[0045] The polyols used in accordance with the inventions are commercially available compounds that can be obtained from Covestro Deutschland AG under the trade names Baycoll® or Desmophen®.

[0046] Aromatic and aliphatic diisocyanates are preferred. Particularly preferred are toluene-2,4-diisocyanate, toluene-2,6-diisocyanate, phenylene diisocyanate, 4,4-diphenylmethane diisocyanate, methylene bis(4-phenyl isocyanate), naphthalene-1,5-diisocyanate, tetramethylene-1,4-diisocyanate and / or hexamethylene-1,6-diisocyanate, with toluene-2,4-diisocyanate and toluene-2,6-diisocyanate being especially preferred.

[0047] Commercially available compounds can be used as diisocyanates, for example the compounds sold by Covestro Deutschland AG under the trade name Desmodur®.

[0048] In a further embodiment of the invention, the composition additionally contains at least one diamine and / or diol.

[0049] Diamines used for chain elongation include 2-methylpropyl-3,5-diamino-4-chlorobenzoate, bis-(4,4'-amino-3-chlorophenyl)methane, 3,5-dimethylthio-2,4-toluenediamine, 3,5-dimethylthio-2,4-toluenediamine, and 3,5-diethyl-2,4-toluenediamine.

[0050] 3,5-Diethyl-2,6-toluenediamine, 4,4'-Methylene-bis-(3-chloro-2,6-diethylaniline) and 1,3-

[0051] Propanediol bis(4-aminobenzoate) preferred.

[0052] Preferred diols include butanediol, neopentyl glycol, hexanediol, propylene glycol, dipropylene glycol, diethylene glycol and / or cyclohexanedimethanol.

[0053] Commercially available compounds can be used as diamines or diols, for example those sold by Lanxess Deutschland GmbH under the trade name Addolink®.

[0054] Dibutyltin dilaurate or triethylenediamine in dipropylene glycol are preferably used as catalysts.

[0055] Commercially available compounds can be used as PU catalysts, for example the compounds sold by Lanxess Deutschland GmbH under the trade name Addocat®.

[0056] In a preferred embodiment of the present invention, the inventive mixture containing tertiary araliphatic carbodiimide and diazaphospholidine oxide is used in an amount of 0.1 to 2 wt.%, preferably 0.5 to 1.5 wt.%, based on the total amount of the mixture for the production of polyurethane.

[0057] The polyurethanes obtained in this process, especially TPU, are characterized by excellent hydrolysis resistance.

[0058] The present invention therefore also relates to compositions containing

[0059] (a) at least one tertiary araliphatic carbodiimide, preferably a carbodiimide of formula 1a or 1b, particularly preferably of formula 1a or 11b,

[0060] (b) at least one diazaphospholide oxide of formula (III) and

[0061] (c) At least one polyurethane, preferably thermoplastic polyurethane

[0062] In a preferred embodiment, the polyurethane composition contains a proportion of component (a) of 0.1 to 2 wt.%, preferably of 0.5 to 1.5 wt.% and a proportion of component (b) of 0.0005 wt.% to 0.04 wt.%, preferably of 0.004 wt.% to 0.02 wt.%, each based on the total composition.

[0063] The present invention further relates to a process for the production of hydrolysis-stabilized polyurethane, preferably hydrolysis-stabilized TPU, characterized in that, in a first step, tertiary araliphatic carbodiimides are produced by a process according to the invention and these are added to a reaction mixture for the production of a polyurethane or TPU without significant separation of diazaphospholidine oxides of formula (III) and the mixture obtained thereby is then reacted to form a polyurethane or TPU.

[0064] The term "without substantial separation" includes process steps aimed at removing the catalyst. This excludes purification steps, particularly those for the removal of solvents, which reduce the amount of catalyst in the reaction mixture obtained in the first step by less than 30 wt.%, preferably less than 50 wt.%, particularly preferably less than 70 wt.%, and most preferably by less than 90 wt.%. In a generally preferred embodiment of the invention, the reaction mixture obtained in the first step, containing tertiary araliphatic carbodiimides and diazaphospholidine oxides of formula (III), is used without further work-up.

[0065] The reaction mixture for the production of a polyurethane or TPU typically contains polyols, preferably polyester polyols, polyisocyanates and optionally one or more polyurethane catalysts.

[0066] In principle, the addition of the mixture obtained in the first step, containing tertiary araliphatic carbodiimides and diazaphospholidine oxides of formula (III), to the reaction mixture for the production of a polyurethane or TPU can take place at any stage of the manufacturing process of a thermoplastic polyurethane, i.e., also at a stage in which the polymerization has already begun or when prepolymers are used.

[0067] Another object of the present invention is the use of mixtures containing tertiary araliphatic carbodiimides and diazaphospholidine oxides of formula (III) in processes for the production of hydrolysis-stabilized polyurethanes and TPU.

[0068] A further object of the present invention is the use of the mixture containing tertiary araliphatic carbodiimides and diazaphospholidine oxides of formula (III) in thermoplastic polyurethanes (TPU), polyurethane elastomers, PU adhesives, PU casting resins, PU foams, or PU coatings for wood, leather, artificial leather, and textiles as protection against hydrolytic degradation. The following examples serve to illustrate the invention without being limiting.

[0069] Examples of implementation:

[0070] Example 1: Preparation of a sterically hindered aromatic carbodiimide by the reaction of the compound 1,3,5-triisopropyl-2,4-phenyl diisocyanate (TRIDI) with methylphospholene oxide (MPO), (comparison)

[0071] Example 2: Preparation of a sterically hindered araliphatic carbodiimide by the reaction of the compound m-tetramethylxylene diisocyanate (TMXDI) with methylphospholene oxide (MPO), (comparison)

[0072] Example 3: Preparation of a sterically hindered aromatic carbodiimide by the reaction of the compound 1,3,5-triisopropyl-2,4-phenyl diisocyanate (TRIDI) with 1,2,3-trimethyl-2-oxo-1,3,2-diazaphospholidine, (comparison)

[0073] Example 4: Preparation of an aliphatic carbodiimide by the reaction of the compound dicyclohexylmethane-4,4'-diisocyanate (H12MDI) with 1,2,3-trimethyl-2-oxo-1,3,2-diazaphospholidine, (comparison)

[0074] Example 5: Preparation of a sterically hindered araliphatic carbodiimide by reacting the compound m-tetramethylxylene diisocyanate (TMXDI) with 1,2,3-trimethyl-2-oxo-1,3,2-diazaphospholidine (according to the invention).

[0075] General manufacturing instructions for examples 1 - 5:

[0076] Thirty grams of the isocyanate-containing compounds m-tetramethylxylene diisocyanate (TMXDI), dicyclohexylmethane-4,4'-diisocyanate (H12MDI), or 1,3,5-triisopropyl-2,4-phenyl diisocyanate (TRIDI) were weighed into a 100 ml three-necked flask equipped with an internal thermometer, reflux condenser, and inert gas inlet. The wt.% of the respective catalyst was then added according to Table 1. During the heating phase, a gentle stream of argon was passed over the vapor phase. When CO2 evolution began, the inert gas was shut off. The carbodiimidation was carried out at 180 °C with stirring until the target NCO content of 12 wt.% was reached. The formation of carbodiimide groups (NCN) was confirmed by IR spectroscopy. The reaction mixture was then cooled and the remaining NCO groups were reacted with methyl polyethylene glycol (MPEG) (Mw approx. 500 g / mol). Table 1: Reaction times for the synthesis of the carbodiimide Surprisingly, the diazaphospholidine oxide used for the carbodiimidation of TMXDI exhibits high catalyst activity and leads to similar NCO concentrations after a 12-hour reaction time, whereas the catalyst activity for the sterically hindered aromatic isocyanate TRIDI and the sterically hindered aliphatic isocyanate H12MDI was low. Furthermore, compared to the prior art, the catalyst according to the invention does not need to be separated after synthesis by filtration, extraction, thermal decomposition, and / or distillation and can be used directly in PU applications, such as for stabilizing thermoplastic polyurethane elastomers or polyurethane foams. PU reactivity test for interfering side effects

[0077] One part polycarbodiimide and nine parts 4,4'-methylene di(phenyl isocyanate) (MDI) were placed in a 250 ml four-necked flask. The mixture was then inerted with nitrogen. It was subsequently heated to 80 °C and stirred. Foaming and gas evolution were checked. After 24 hours, the viscosity of the final sample was also assessed.

[0078] The properties of the polymeric carbodiimides obtained in Examples 6 and 7 are shown in Table 2:

[0079] Table 2: PU reactivity test

[0080] Cf. = comparative example; Inf. = according to the invention

[0081] Tests in PU hot melt adhesive

[0082] The hot melt adhesive was produced as follows:

[0083] Dynacoll®, which is commercially available from Evonik, is a linear copolyester with primary hydroxyl functionalities and a medium molecular weight.

[0084] First, the copolyester is evacuated for 30 minutes at 120 °C. Then, 11.67 wt% diphenylmethane diisocyanate (MDI), based on the total formulation, is added, and the mixture is reacted for 60 minutes at 120 °C. Subsequently, the respective carbodiimides listed in Table 3 are incorporated into the hot melt adhesive, and an aging time of 1 hour for the additives is ensured. The hot melt adhesives produced and added in this way were subjected to temperature aging at 130 °C for 48 hours in a cartridge. The thermally aged product was filled into an aluminum cartridge (light- and moisture-proof) and aged in a convection oven at 130 °C for 48 hours.

[0085] After aging, the foaming behavior of the samples was visually assessed. The measurement results are summarized in Table 3:

[0086] Table 3:

[0087] V = comparative example; Inv. = according to the invention

Claims

1. Process for the preparation of tertiary araliphatic carbodiimides from araliphatic isocyanates, wherein the araliphatic isocyanates are reacted in the presence of one or more diazaphospholidine oxides of formula (III), in which R 1 , R 2 , R 3 are independently selected from Ci-Ce-alkyl, cyclohexyl and aryl and wherein preferably R 1 , R 2 , R 3 Methyl are.

2. A process for the preparation of tertiary araliphatic carbodiimides according to claim 1, wherein the tertiary araliphatic carbodiimides are of formula (1a) or the formula (Ib) correspond to, wherein n corresponds to a number from 0 to 20, preferably 0 or 3 to 8, particularly preferably 0 or 4 to 5, I corresponds to a number from 1 to 20, preferably from 3 to 8, particularly preferably from 4 to 5, R 1Independently selected from compounds of the formula laa, lab, lac or lad, compounds of the formula lab are preferred. R 4 and R 5 The residues R were selected independently of each other from Ci-C4 alkyl. 6 and R 7 Selected independently from Ci - C4-alkyl, Ci - C4-Alkoxy, a, b, c represents a number from 0 to 4, preferably 0, R 2 and R 3 are independently selected from -O-(Ci - C2o-alkyl), -O-(Ci - C2o-alkenyl), -O-(Cs - C2o-cycloalkyl), -O-aryl, -O-(C? - C2o-alkyaryl), -O-[(CH2)k- O] g -R 8 , with k= 1-3, g = 0-12 and R 8 = H or Ci-C4-alkyl.

3. A process for the preparation of tertiary araliphatic carbodiimides according to one or more of claims 1 to 3, wherein the carbodiimides are selected from bis[3-isopropenyl-α,α-dimethylbenzyl]carbodiimide (Ha) wherein I corresponds to a number from 1 to 20, preferably from 3 to 8, most preferably from 4 to 5, and m corresponds to a number from 1 to 20, preferably from 3 to 15, most preferably from 5 to 11.

4. A process for the preparation of tertiary araliphatic carbodiimides according to one or more of claims 1 to 3, wherein 3-isopropenyphenyl-a,a-dimethylbenzyl isocyanate and / or m-tetramethylxylol diisocyanate are used as araliphatic isocyanates.

5. A process for the production of tertiary araliphatic carbodiimides according to one or more of claims 1 to 4, wherein the reaction takes place at temperatures of 160 to 220°C, preferably 180 to 200°C, particularly preferably 180 to 190°C.

6. A process for the production of tertiary araliphatic carbodiimides according to one or more of claims 1 to 5, wherein the reaction is carried out in the presence of 0.5 to 2 wt.%, preferably 0.8 to 1.5 wt.%, particularly preferably 1 to 1.2 wt.% based on the total amount of araliphatic isocyanates.

7. A process for the production of tertiary araliphatic carbodiimides according to one or more of claims 1 to 6, wherein, after carbodiimidation of the araliphatic isocyanates to carbodiimides, the terminal free isocyanate- Groups of carbodiimides are reacted with aliphatic and / or aromatic alcohols and / or alkoxypolyoxyalkylene alcohols.

8. Mixtures containing tertiary araliphatic carbodiimides and, based on the araliphatic carbodiimides, 0.5 to 2 wt.%, preferably 0.8 to 1.5 wt.%, particularly preferably 1 to 1.2 wt.% diazaphospholidine oxides of formula (III), in which R 1 , R 2 , R 3 are independently selected from Ci-Ce-alkyl, cyclohexyl and aryl and preferably R 1 , R 2 , R 3 Methyl are obtainable according to one or more of claims 1 to 7.

9. Use of mixtures according to claim 8 for the production of hydrolysis-stabilized polyurethane (PU), preferably hydrolysis-stabilized thermoplastic polyurethane (TPU).

10. Process for the production of hydrolysis-stabilized polyurethane (PU), preferably hydrolysis-stabilized thermoplastic polyurethane (TPU), characterized in that in a first step tertiary araliphatic carbodiimides are produced according to one or more of claims 1 to 7 and these are brought into contact in a further step with polyols, preferably polyester polyols, polyisocyanates and optionally one or more polyurethane catalysts without significant separation of the diazaphospholidine oxide(s) of formula (III) and are reacted to form hydrolysis-stabilized polyurethane (PU) or hydrolysis-stabilized thermoplastic polyurethane (TPU).

11. Polyurethane obtainable by the method according to claim 10.

12. Thermoplastic polyurethane obtainable by the method according to claim 11 13. Compositions containing (a) at least one tertiary araliphatic carbodiimide, preferably one Carbodiimide of formula a1a or b1b, particularly preferably of formula I a1a or b1b, (b) at least one diazaphospholide oxide of formula (III) and (c) at least one polyurethane, preferably thermoplastic polyurethane.

14. Composition according to claim 13, wherein the proportion of component (a) is from 0.1 to 2 wt.%, preferably from 0.5 to 1.5 wt.% and a proportion of component (b) is from 0.0005 wt.% to 0.04 wt.%, preferably from 0.004 wt.% to 0.02 wt.%, in each case based on the total composition.

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