Polyester carbonates from alicyclic diacids, 1,4:3,6-dianhydrohexitol, and further aliphatic dihydroxy compounds

Abstract

The present invention relates to a process for preparing polyestercarbonates based on cycloaliphatic diacids and at least one 1,4:3,6-dianhydrohexitol and at least one further aliphatic dihydroxy compound, to the polyestercarbonates prepared according to the process, and to molding compounds and molded articles containing the polyestercarbonates. The process according to the invention is a direct synthesis in which all structural elements forming the subsequent polyestercarbonate are already present as monomers in the first process step.

Description

[Technical Field]

[0001] The present invention relates to a copolyester carbonate formed from an alicyclic diacid and 1,4:3,6-dianhydrohexitol containing at least one additional aliphatic diol, and also relates to a method for preparing the corresponding polyester carbonate. [Background technology]

[0002] Polyesters, polycarbonates, and polyester carbonates are known to possess excellent properties in terms of mechanical properties, thermal deformation stability, and weather resistance. Depending on the monomer used, each polymer group has certain key characteristics that characterize such materials. For example, polycarbonates, in particular, have excellent mechanical properties, while polyesters often exhibit superior chemical stability. Depending on the selected monomer, polyester carbonates exhibit property profiles from both of the aforementioned groups.

[0003] While aromatic polycarbonates or polyesters often exhibit excellent property profiles, they have disadvantages in terms of aging resistance and weather resistance. For example, they yellow due to ultraviolet light absorption, and in some cases, these thermoplastic materials become brittle. In this respect, aliphatic polycarbonates and polyester carbonates have superior properties, particularly superior aging resistance and / or weather resistance, as well as superior optical properties (e.g., transmittance).

[0004] A disadvantage of aliphatic polycarbonates or polyester carbonates is often their low glass transition temperature. Therefore, it is advantageous to use alicyclic alcohols as (co)monomers. Examples of such alicyclic alcohols include TCD alcohol (tricyclodecanedimethanol; 8-(hydroxymethyl)-3-tricyclo[5.2.1.0 2,6Examples of bio-based diols based on 1,4:3,6-dianhydrohexitol include 1,4:3,6-dianhydrohexitol (decanyl)methanol, cyclohexanediol, cyclohexanedimethanol, and isosorbide and its isomers isomannide and isoidide. To further increase the glass transition temperature, alicyclic acids such as 1,2-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, or 1,4-cyclohexanedicarboxylic acid, or corresponding naphthalene derivatives can be used as (co)monomers. In this case, a polyester or polyester carbonate can be obtained depending on the selection of reactants. This application relates to copolyester carbonates with improved properties based on 1,4:3,6-dianhydrohexitol such as isosorbide and its isomers, and further, alicyclic diacitors comprising at least one further dihydroxy compound. The present invention further relates to a method for preparing these copolyester carbonates characterized by the direct reaction of the raw materials and without requiring any difficult-to-handle raw materials such as phosgene.

[0005] Polyesters of cyclohexanedicarboxylic acid and isosorbide are described in Non-Patent Document 1. However, the present invention preferably relates to polyester carbonates.

[0006] Polyesters are prepared on an industrial scale, for example, by transesterification of corresponding ester-containing monomers with diols. For example, starting with dimethyl esters of diacides, polyesters of 1,4-cyclohexanedimethanol and 1,4-cyclohexanedicarboxylic acid are produced (a blend of this polyester with polycarbonate: DuPont's Xyrex®).

[0007] However, with respect to transesterification reactions, phenyl esters are far more reactive than their aliphatic analogs. Patent documents 1 and 2 describe methods for preparing polyester carbonates having phenyl esters as an intermediate step.

[0008] Example 1 of Patent Document 1 describes obtaining the corresponding ester by the direct reaction of a diacid with phenol. Example 2 of Patent Document 1 describes the reaction of a dimethyl ester with phenol. However, both modifications for the preparation of phenyl esters still have room for improvement in terms of yield. Next, the preparation of polyester carbonate is carried out. Therefore, this document describes a two-step method with corresponding disadvantages in several stages, such as complexity, increased cost, and the need for multiple purification steps.

[0009] Patent document 2 describes the preparation of diphenyl esters in a solvent using phosgene. Since the subsequent reaction to obtain aliphatic polyester carbonates does not require phosgene, combining the phosgene process and the transesterification process in a single plant is highly disadvantageous. Therefore, the method described in patent document 2 is also not optimal. Here again, a two-step method is described.

[0010] The two-step method is similarly described in Patent Documents 3, 4 (5), and 6. This means that all of these documents consistently describe obtaining the ester by the reaction of diacids. Subsequently, the initially isolated ester is converted to a polyester carbonate.

[0011] Patent document 7 describes an isosorbide unit and an aliphatic C 14 ~C 44 diacid, aliphatic C 14 ~C 44Disclosed is an isosorbide-based polycarbonate comprising aliphatic units derived from diols or combinations thereof, and optionally isosorbide units and additional units different from the aliphatic units, wherein the isosorbide units, aliphatic units, and additional units are, respectively, carbonates or combinations of carbonate units and ester units. The common disadvantages of aliphatic polycarbonates or polyester carbonates have already been discussed above. In the examples, polymers derived from combinations of isosorbide, alicyclic diacids, and additionally aliphatic diols are not prepared. Furthermore, activated carbonates are used for transesterification.

[0012] Non-patent document 2 states that polyesters formed from cyclohexanedicarboxylic acid and isosorbide cannot be obtained from cyclohexanedioic acid or cyclohexanedimethyl ester (or only very low molecular weights can be obtained), and can only be produced from acid chlorides of cyclohexanedicarboxylic acid.

[0013] For example, Patent Document 8 describes a simple preparation of aromatic polyester carbonates. This document reveals a direct synthesis or one-pot synthesis, i.e., a synthesis in which all structural elements forming the subsequent polyester carbonate are already present as monomers at the start of the synthesis. The monomers used here are aromatic dihydroxy compounds such as bisphenol A, carboxylic acid diesters, and aromatic diacides or linear aliphatic diacides. As a result of the fact that only aromatic polyester carbonates are prepared in this document, a temperature of 300°C can be used in the condensation reaction while removing the phenols that are formed. In the preparation of aliphatic polyester carbonates, the use of such a temperature is not possible, because under such thermal stress, aliphatic diols tend to undergo elimination and / or thermal decomposition. However, at the same time, high temperatures are necessary to reach the desired high molecular weight. Here, the difference in reactivity between aliphatic diols and aromatic diols becomes particularly apparent. For example, it is known from the literature that isosorbide is rarely completely incorporated into the polymer, and rather, up to 25% of isosorbide is lost during the polymerization reaction depending on the selected reaction conditions. Therefore, it is not immediately possible to apply the reaction conditions for aromatic diols to aliphatic diols. This is particularly evident from the fact that the reaction time for polycondensation (corresponding to step (ii)) in Patent Document 8 is significantly longer at higher temperatures than the reaction time observed according to the present invention.

[0014] Similarly, Patent Documents 9 and 10 use aromatic units and correspondingly high temperatures. For the reasons stated above, the teachings in the above documents cannot be carried over to aliphatic units.

[0015] Patent document 11 describes a method for preparing polyesters containing isosorbide units. In this method, isosorbide is dissolved in water, as it should be added to an existing reactor in the simplest possible manner. Therefore, this document primarily relates to the preparation of polyesters and further requires the presence of a solvent.

[0016] Patent document 12, which is an unpublished application, discloses a one-pot synthesis of polyester carbonates comprising an alicyclic dicarboxylic acid, a diaryl carbonate, and an aliphatic dihydroxy compound.

[0017] The polyester carbonates described in Patent Documents 1 and 2 have high glass transition temperatures. However, the structure of these polyester carbonates is very rigid. This is a result of the isosorbide structure being incorporated into the polymer chain by condensation, in particular. Due to its rigid nature, the bicyclic substructure increases the glass transition temperature, but the polymer chain becomes less flexible, which can, in principle, lead to disadvantages. Park et al. state that a higher amount of isosorbide in the polymer leads to a decrease in molecular weight (Non-Patent Document 3). The authors state that the increase in molecular weight is hindered by the high melt viscosity. Failure to reach the critical molecular weight can result in insufficient mechanical properties. This is particularly important for inflexible polymer chains. Rigid chains require a relatively high molecular weight to be able to entangle. Failure to achieve this results in brittle behavior (critical entanglement molecular weight).

[0018] Cyclohexanedicarboxylic acid somewhat enhances flexibility, but the overall structure of the polymer chain still remains very rigid. This can pose a disadvantage during the preparation of the polymer. Due to the non-flexible nature, as the molecular weight increases, it becomes more difficult for the reaction partners (chain ends) to find each other. As described above, this limits the molecular weight. Furthermore, due to the rigid nature, a sharp increase in viscosity is caused during polymer synthesis. To compensate for this, during polymer preparation, the temperature is often increased at the final stage of polycondensation to achieve better fluidity. However, this is only possible to a limited extent in the case of aliphatic polymers. This is because, for example, compared to aromatic polyesters or polycarbonates, the thermal stability is significantly lower. Since the increase in viscosity cannot be compensated by increasing the temperature, poor mixing and low surface renewal are brought about. Therefore, the condensation product (e.g., phenol) can no longer be removed, and the polycondensation is interrupted.

[0019] To achieve better surface renewal, Patent Document 6 describes the use of horizontal polymer reactors such as polymer kneaders. Since these exert a high shear force on the polymer, surface renewal can be enhanced and polycondensation can be continued. However, a high shear force places a great load on non-flexible polymers.

[0020] A high shear stress can cause damage, which may manifest as a deterioration of optical and mechanical properties.

Prior Art Documents

Patent Documents

[0021]

Patent Document 1

Patent Document 2

Patent Document 3

Patent Document 4

[0022] [Non-Patent Document 1] Oh et al., in Macromolecules 2013, 46, 2930-2940 [Non-Patent Document 2] Kricheldorf et al., (Macromol. Chem. Phys 2010, 211, 1206-1214) [Non-Patent Document 3] S. A. Park et al. Polymer 2017, 116, 153 - 159; pp. 155 / 156 [Summary of the Invention] [Problems to be Solved by the Invention]

[0023] Therefore, starting from this prior art, the object of the present invention was to provide a method for preparing a polyester carbonate comprising at least one 1,4:3,6-dianhydrohexitol and at least one alicyclic dicarboxylic acid, characterized by good surface renewal during preparation. Better surface renewal is supported, for example, by a higher molecular weight that can be achieved. In particular, this should make it possible to achieve a sufficiently high molecular weight of the polyester carbonate. The term "sufficiently high molecular weight" is understood to mean a polymer having a relative solution viscosity of greater than 1.22, preferably 1.25 to 1.65, more preferably 1.28 to 1.63, and particularly preferably 1.30 to 1.62, as measured in each case using an Ubbelohde viscometer at a concentration of 5 g / l in dichloromethane at 25°C. Therefore, furthermore, the polyester carbonate according to the present invention should have better processing properties and good mechanical properties. A further object was to provide the simplest possible method for preparing polyester carbonate by melt transesterification. In this context, "simple" is understood to mean a method that requires fewer equipment, involves fewer steps, especially fewer purification steps, and / or is therefore economically and environmentally advantageous. In particular, the method according to the present invention should not require difficult-to-handle starting materials, especially phosgene. [Means for solving the problem]

[0024] At least one, preferably all, of the above-mentioned problems have been solved by the present invention. Surprisingly, it has been found that polyester carbonates can be synthesized by melt transesterification from at least one alicyclic dicarboxylic acid, at least one diaryl carbonate, at least one 1,4:3,6-dianhydrohexitol, and at least one further aliphatic dihydroxy compound in direct synthesis or one-pot synthesis in which all structural elements forming the subsequent polyester carbonate are already present as monomers at the start of the synthesis. However, it has been found that polymers having appropriate molar mass and therefore appropriate mechanical properties are obtained particularly from the molar ratio of the alicyclic dicarboxylic acid and all aliphatic dihydroxy compounds. Firstly, despite the preconceptions described in the prior art, it was surprising that direct synthesis also works for the reaction of alicyclic dicarboxylic acid, 1,4:3,6-dianhydrohexitol, at least one further aliphatic dihydroxy compound (also called "aliphatic diol" in the present invention), and diaryl carbonate. Furthermore, it was quite surprising that the molar ratio of all aliphatic dihydroxy compounds to all alicyclic dicarboxylic acids affected the property of increasing the molecular weight of the polymer. This allowed us to find a method that is particularly simple, i.e., requires little equipment, involves few steps, especially fewer purification steps, and is therefore economically and environmentally advantageous, for obtaining polyester carbonates from alicyclic diacids, 1,4:3,6-dianhydrohexitol, and at least one further aliphatic dihydroxy compound.

[0025] Furthermore, it was found that the incorporation of small amounts of additional aliphatic dihydroxy compounds, particularly branched aliphatic dihydroxy compounds, enhanced surface renewal during synthesis. It was surprising that even the incorporation of small amounts of additional diols significantly increased surface renewal, and therefore molecular weight. It was particularly surprising that branched diols were readily incorporated into the polymer chain by condensation despite steric hindrance. Those skilled in the art would have predicted that steric hindrance would prevent an increase in molecular weight.

[0026] Furthermore, a novel polyester carbonate was obtained that has a different structure from the polyester carbonates previously described in the prior art, namely, a different statistical distribution of structural elements.

[0027] A method for preparing polyester carbonates according to the present invention can be schematically described as follows, for example, by the reaction of cyclohexanedicarboxylic acid, isosorbide, an additional diol HO-R-OH, and diphenyl carbonate: [ka] (These three specific starting materials are listed solely for illustrative purposes and should not be understood as limiting.)

[0028] In the direct synthesis according to the present invention, gas generation (leakage of carbon dioxide) was initially observed. After the gas generation had essentially subsided, a sample of the mixture was taken, and analysis demonstrated that oligomers had already been formed. These oligomers were condensed in a further step to obtain the polyester carbonate according to the present invention. Examples of the present invention show that, as in the prior art, when only one derivative of cyclohexanedicarboxylic acid reacts with diphenyl carbonate, isosorbide, and further diols (for example), the statistical distribution of carbonate blocks and ester blocks in these oligomers (see scheme above) is already different from the pure statistical distribution of the blocks. Furthermore, the reactivity of such oligomers differs from the reactivity of pure cyclohexanediphenyl ester, isosorbide, further diols, and pure diphenyl carbonate. Therefore, the final result of the method of the present invention is to obtain polymers in which the statistical distribution of various blocks differs from the statistical distribution of polymers obtained from cyclohexanediphenyl ester, isosorbide, further diols, and diphenyl carbonate.

[0029] Therefore, the present invention relates to a method for preparing polyester carbonate by molten transesterification, (i) a step of reacting at least one alicyclic dicarboxylic acid and at least one diaryl carbonate with at least one catalyst in the presence of a mixture of dihydroxy compounds comprising (A) at least one 1,4:3,6-dianhydrohexitol and (B) at least one further aliphatic dihydroxy compound, (ii) A step of further condensing the mixture obtained from step (i) while removing at least the chemical compounds that were removed during condensation, Includes, The present invention provides a method characterized in that the molar ratio of all dihydroxy compounds present in method step (i) to all alicyclic dicarboxylic acids present in method step (i) before the reaction in method step (i) is 1:0.6 to 1:0.05, preferably 1:0.55 to 1:0.1, and particularly preferably 1:0.5 to 1:0.15.

[0030] According to the present invention, step (i) involves the reaction of at least one alicyclic dicarboxylic acid with at least one diaryl carbonate. However, according to the present invention, further reactions cannot be ruled out as a result of the presence of at least one 1,4:3,6-dianhydrohexitol (hereinafter also referred to as component (A)) and at least one further aliphatic dihydroxy compound (hereinafter also referred to as component (B)). In fact, examples have demonstrated that as early as step (i), oligomers with a mass interval in a MALDI-ToF mass spectrometer corresponding to units formed from component (A) and / or component (B) and the carbonate (with two hydroxyl groups lost) are formed. This means that further reactions other than the formation of diesters may occur in step (i). However, according to the present invention, this also means that the reaction of all present alicyclic dicarboxylic acids with stoichiometric equivalents of diaryl carbonates does not need to have occurred and been completed before the start of step (ii). However, according to the present invention, it is preferable to perform step (i) until a substantial reduction in gas formation can be observed, and only then begin step (ii) by, for example, applying a vacuum to remove the chemical compounds desorbed during condensation. However, as already stated above, optionally, step (i) and step (ii) cannot be clearly distinguished from each other according to the present invention.

[0031] Method step (i) The method according to the present invention is called direct synthesis or even one-pot synthesis. This is because, in step (i) of the method, all structural elements that will form the subsequent polyester carbonate are already present as monomers. Preferably, according to the present invention, all aliphatic dihydroxy compounds (components (A) and (B) in each case), all alicyclic dicarboxylic acids, and all diaryl carbonates are present in this step, even if there are more than just the dihydroxy compounds, alicyclic dicarboxylic acids, and / or diaryl carbonates of components (A) and (B). Therefore, according to the present invention, it is preferable that all monomers that will be condensed to form a polyester carbonate in step (ii) are already present during step (i). The present invention also includes embodiments in which a small proportion of at least one diaryl carbonate is additionally added in step (ii). This can be used selectively to reduce the OH-terminated group content of the resulting polyester carbonate. Such an approach is described, for example, in Japanese Patent Application Publication No. 2010-077398. However, in this case, if all the structural elements that form the subsequent polyester carbonate are still present as monomers in step (i) and no further structural elements are added, then the at least one diaryl carbonate added in small amounts in step (ii) must correspond to the at least one diaryl carbonate present in step (i). Therefore, in this sense, this method can still be called direct synthesis or one-pot synthesis.

[0032] Furthermore, according to the present invention, the presence of aromatic dihydroxy compounds and / or aromatic dicarboxylic acids in step (i) of the method is not excluded. However, these are preferably present only in small amounts. In step (i) of the method, it is particularly preferable that there be a further presence of up to 20 mol%, more preferably up to 10 mol%, and very particularly preferably up to 5 mol%, of aromatic dihydroxy compounds (component (C)) relative to the total molar amount of dihydroxy compounds used. Similarly, in step (i), it is also particularly preferable that, optionally in addition to aromatic dihydroxy compounds, there be a further presence of up to 20 mol%, more preferably up to 10 mol%, and very particularly preferably up to 5 mol%, of aromatic dicarboxylic acids relative to the total molar amount of dicarboxylic acids used. In these cases, according to the present invention, aliphatic polyester carbonates are still preferred. However, it is particularly preferable not to use aromatic dihydroxy compounds in step (i). Similarly, it is preferable not to use aromatic dicarboxylic acids in step (i). Similarly, it is preferable not to use either aromatic dihydroxy compounds or aromatic dicarboxylic acids in step (i). Generally, aromatic compounds in polyester carbonates reduce their UV stability and weather resistance. This is particularly disadvantageous for outdoor applications. Furthermore, aromatic components in polyester carbonates can reduce the surface hardness of molded articles produced from them, sometimes necessitating coating. In addition, diphenyl esters of aromatic acids that may form as intermediates are stable intermediates that can, for example, slow down polycondensation. As a result, the use of additional specific catalysts may be required in some cases.

[0033] These additional aromatic dihydroxy compounds (component (C)) are preferably bisphenol A, 1,1-bis(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane, 4,4'-dihydroxydiphenyl (DOD), 4,4'-dihydroxydiphenyl ether (DOD ether), bisphenol B, bisphenol M, bisphenol (I) to bisphenol (III): [ka] (In these formulas (I) to (III), R' is selected from the group consisting of C1-C4 alkyl, aralkyl, or aryl, preferably methyl or phenyl, and very preferably methyl, in each case.)

[0034] These additional aromatic dicarboxylic acids are preferably selected from the group consisting of isophthalic acid, terephthalic acid, 2,5-franzicarboxylic acid, and 2,6-naphthalenedicarboxylic acid. It is known that even small amounts of these aromatic diacides can reduce the water absorption of aliphatic polyester carbonates.

[0035] According to the present invention, in step (i) of the method, at least one 1,4:3,6-dianhydrohexitol is used as component (A). As is known to those skilled in the art, 1,4:3,6-dianhydrohexitol is generally selected from the group consisting of isomannides, isoidides, and isosorbides. This may include bio-based structural elements that have all the advantages of bio-based monomers and the resulting polymers (for example, they can be obtained from renewable raw materials and are therefore more sustainable). The method according to the present invention is particularly characterized in that at least one 1,4:3,6-dianhydrohexitol is isosorbide. It is preferable that component (A) consists of isosorbide.

[0036] According to the present invention, in step (i) of the method, at least one further aliphatic dihydroxy compound (component (B)) is used. Preferably, component (B) consists of two further aliphatic dihydroxy compounds. Similarly, preferably, component (B) consists of one further aliphatic dihydroxy compound. Therefore, it is particularly preferable that component (A) consists of isosorbide and component (B) consists of further aliphatic dihydroxy compounds. Optionally, component (C) containing an aromatic dihydroxy compound (see above) may be present in the mixture of dihydroxy compounds.

[0037] Here, at least one further aliphatic dihydroxy compound is given chemical formula (I): HO-X-OH (I) It is preferable that the formula has (wherein X represents a linear alkylene group having 2 to 22, preferably 2 to 15, particularly preferably 2 to 10 carbon atoms, which can be optionally interrupted by at least one heteroatom, a branched alkylene group having 4 to 20, preferably 5 to 15 carbon atoms, which can be optionally interrupted by at least one heteroatom, or a cycloalkylene group having 4 to 20, preferably 5 to 15 carbon atoms, which can be optionally interrupted by at least one heteroatom, where the cycloalkylene group may optionally contain a plurality of rings and may optionally be branched in each case).

[0038] According to the present invention, when X is a linear alkylene group that can be optionally interrupted by at least one heteroatom, it preferably has 2 to 15 carbon atoms, particularly preferably 2 to 12, very particularly preferably 2 to 11, particularly preferably 2 to 10, more preferably 2 to 6, and more preferably 3 to 4 carbon atoms. The heteroatom that can optionally interrupt the alkylene group is preferably oxygen or sulfur, particularly preferably oxygen. Particularly preferably, the alkylene group contains only one heteroatom or does not contain a heteroatom. When there is at least one heteroatom present in the alkylene group, the indicated number of carbon atoms refers to the total number of carbon atoms in the alkylene group. For example, the group -CH2-CH2-O-CH2-CH2- contains 4 carbon atoms. According to the present invention, a linear alkylene group that can be optionally interrupted by at least one heteroatom preferably has fewer than 12 carbon atoms, particularly preferably fewer than 10. Particularly preferably, the alkylene group does not contain any heteroatoms.

[0039] According to the present invention, the above description applies to heteroatoms when X is a branched alkylene group having 4 to 20, preferably 5 to 15, particularly preferably 5 to 11, and very preferably 5 to 10 carbon atoms, which can be optionally interrupted by at least one heteroatom. The heteroatom that can optionally interrupt the branched alkylene group is preferably oxygen or sulfur, particularly preferably oxygen. Particularly preferably, the branched alkylene group contains only one heteroatom or contains no heteroatoms. Particularly preferably, the branched alkylene group has no heteroatoms at all. The term “branched” is understood to refer to branching in an aliphatic carbon chain known to those skilled in the art. This means that the branched alkylene group preferably contains at least one tertiary carbon atom and / or at least one quaternary carbon atom. Two or more branches may be present in the branched alkylene group. The branches have a chain length of preferably 1 to 5 carbon atoms, particularly preferably 1 to 4, and very preferably 1 to 3 carbon atoms. These carbon atoms in the branching are taken into account in the total number of carbon atoms in the branched alkylene group. This means, for example, that the branched alkylene group -CH2-C(CH3)2-CH2- has 5 carbon atoms.

[0040] According to the present invention, the above description applies to the heteroatom when X is a cycloalkylene group having 4 to 20, preferably 5 to 15 carbon atoms, which can be optionally interrupted by at least one heteroatom, and the cycloalkylene group may optionally contain multiple rings, each of which may optionally be branched. The heteroatom that can optionally interrupt the cycloalkylene group is preferably oxygen or sulfur, particularly preferably oxygen. Particularly preferably, the cycloalkylene group contains only one heteroatom or does not contain a heteroatom. Particularly preferably, the cycloalkylene group has no heteroatoms at all. Preferably, the cycloalkylene group has at least one, preferably one ring, having 4 to 6 carbon atoms. Particularly preferably, the cycloalkylene group has a total of 4 to 20, preferably 5 to 15 carbon atoms, and a ring having 4 to 5 carbon atoms. In this case, the carbon atoms of the ring are considered in the total number of carbon atoms in the cycloalkylene group. This means that the tetramethylcyclobutenyl group has a total of eight carbon atoms and includes a ring having four carbon atoms. The cycloalkylene group may further have at least one branch, which is particularly preferred. If branching is present, it may be present in the alicyclic chain and / or ring, if any. Preferably, the branching is present in the ring. Preferably, X is a cycloalkylene group having 5 to 15 carbon atoms including a ring, which optionally has at least one branch, preferably at least one branch, and has at least one ring, preferably a ring having 4 to 6 carbon atoms, particularly preferably a ring having 4 to 5 carbon atoms.

[0041] Overall, according to the present invention, it is preferable that at least one further aliphatic dihydroxy compound has 2 to 10 carbon atoms.

[0042] Particularly preferred is the method according to the present invention, in which at least one further aliphatic dihydroxy compound is 1,2-cyclohexanediol, 1,3-cyclohexanediol, 1,4-cyclohexanediol, 1,2-cyclohexanedimethanol, 1,3-cyclohexanedimethanol, 1,4-cyclohexanedimethanol, 2,2-bis(4-hydroxycyclohexyl)propane, tetrahydro-2,5-frangimethanol, 2-butyl-2-ethyl-1,3-propanediol, 2-(2-hydroxyethoxy)ethanol, 2,2,4,4-tetramethyl-1,3-cyclobutanediol, 2,2,4-trimethyl-1,3-pentanediol, 2,2-dimethylpropane-1,3-diol, cyclobutane-1,1-diyldimethanol, 8-(hydroxymethyl)-3-tricyclo[5.2.1.0 2,6The present invention is characterized by being selected from the group consisting of ]decanyl]methanol, 1,2-propanediol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, and any desired mixture thereof. In particular, it is preferable that at least one further aliphatic dihydroxy compound is selected from the group consisting of 2-butyl-2-ethyl-1,3-propanediol, 2-(2-hydroxyethoxy)ethanol, 2,2,4,4-tetramethyl-1,3-cyclobutanediol, 2,2,4-trimethyl-1,3-pentanediol, 2,2-dimethylpropane-1,3-diol, cyclobutane-1,1-diyldimethanol, 1,2-propanediol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, and any desired mixture thereof. Similarly, it is preferable that at least one further aliphatic dihydroxy compound is selected from the group consisting of 2-butyl-2-ethyl-1,3-propanediol, 2,2,4,4-tetramethyl-1,3-cyclobutanediol, 2,2,4-trimethyl-1,3-pentanediol, 2,2-dimethylpropane-1,3-diol, cyclobutane-1,1-diyldimethanol, 1,4-butanediol, and any desired mixtures thereof. Most particularly preferred, at least one further aliphatic dihydroxy compound is selected from the group consisting of 2-butyl-2-ethyl-1,3-propanediol, 2,2,4,4-tetramethyl-1,3-cyclobutanediol, 2,2,4-trimethyl-1,3-pentanediol, 2,2-dimethylpropane-1,3-diol, cyclobutane-1,1-diyldimethanol, and any desired mixtures thereof.

[0043] According to the present invention, it has been found that an additional at least one further aliphatic dihydroxy compound can react with the also present at least one diaryl carbonate under the reaction conditions of step (i) of the method of the present invention. This is observed particularly in dihydroxy compounds where the two hydroxyl groups are spatially close to each other (e.g., separated by only two or three carbon atoms). While we do not wish to be bound by theory, it appears that an intramolecular carbonate that is no longer reactive is formed. This means that this intramolecular carbonate no longer participates in the reaction that forms the polyester carbonate. As a result, the amount of at least one further aliphatic dihydroxy compound added at the start of step (i) of the method does not necessarily always correspond to the amount of structural elements in the polyester carbonate derived from the above dihydroxy compound. This amount is generally less, especially in the case of compounds having two hydroxyl compounds spatially close to each other. This is particularly not true for cyclic dihydroxy compounds such as cyclohexanedimethanol. Methods for determining the proportion of structural units in the resulting polyester carbonate are known to those skilled in the art. These proportions are preferably 1 This can be determined by 1H NMR. This method is known to those skilled in the art. Polyester carbonates may be dissolved in, for example, CDCl3, and the corresponding peaks of structural units may be identified. Ratios and proportions can be determined by integration.

[0044] Similarly, according to the present invention, at least one alicyclic dicarboxylic acid is used in step (i) of the method. Here, the at least one alicyclic dicarboxylic acid is of chemical formulas (IIa), (IIb): [ka] (In the formula, Each B independently represents a CH2 group or a heteroatom selected from the group consisting of O and S, preferably a CH2 group or an oxygen atom. Each R1 independently represents an alkylene group having a single bond or 1 to 10 carbon atoms, preferably a single bond or an alkylene group having 1 to 5 carbon atoms, more preferably a single bond, and n is preferably selected from compounds or mixtures thereof (where n is a number between 0 and 3, preferably 0 or 1).

[0045] When R1 represents a single bond, it will be understood that R1 does not contain a carbon atom.

[0046] At least one alicyclic dicarboxylic acid is particularly preferably selected from the group consisting of 1,4-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, 1,2-cyclohexanedicarboxylic acid, tetradihydro-2,5-franglicarboxylic acid, tetradihydro-2,5-dimethylfranglicarboxylic acid, decahydro-2,4-naphthalenedicarboxylic acid, decahydro-2,5-naphthalenedicarboxylic acid, decahydro-2,6-naphthalenedicarboxylic acid, and decahydro-2,7-naphthalenedicarboxylic acid. Any desired mixture can also be used. 1,4-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, or 1,2-cyclohexanedicarboxylic acid are particularly preferred.

[0047] In addition to alicyclic acids, small amounts of further aliphatic acids may also be used. In step (i) of the method, up to 20 mol%, more preferably up to 10 mol%, and very preferably up to 5 mol%, of further aliphatic acids may be present, where it is particularly preferable that these acids are not alicyclic acids. The further aliphatic acids are preferably selected from the group consisting of 2,2,4-trimethyladipic acid, 2,4,4-trimethyladipic acid, 2,2,5-trimethyladipic acid, and 3,3-dimethylglutaric acid.

[0048] Similarly, according to the present invention, in step (i) of the method, at least one diaryl carbonate is used. Here, the at least one diaryl carbonate is of formula (2): [Chemical formula] (wherein, R, R', and R'' are each independently the same or different and represent hydrogen, optionally branched C1-C 34 alkyl, C7-C 34 alkylaryl, C6-C 34 aryl, nitro group, carbonyl-containing group, carboxyl-containing group, or halogen group). It is preferably selected from the group consisting of the compounds. Preferably, R, R', and R'' are each independently the same or different and represent hydrogen, optionally branched C1-C 34 alkyl, C7-C 34 alkylaryl, C6-C 34The term represents an aryl, nitro, carbonyl-containing, or halogen group. At least one diaryl carbonate is preferably diphenyl carbonate, 4-tert-butylphenyl carbonate, di(4-tert-butylphenyl) carbonate, biphenyl-4-ylphenyl carbonate, di(biphenyl-4-yl) carbonate, 4-(1-methyl-1-phenylethyl)phenylphenyl carbonate, di[4-(1-methyl-1-phenylethyl)phenyl] carbonate, bis(methylsalicyl) carbonate, bis(ethylsalicyl) carbonate, bis(propylsalicyl) carbonate, bis(2-benzoylphenyl) carbonate, bis(phenylsalicyl) carbonate, and / or bis(benzylsalicyl) carbonate. At least one diaryl carbonate is preferably diphenyl carbonate, 4-tert-butylphenyl carbonate, di(4-tert-butylphenyl) carbonate, biphenyl-4-ylphenyl carbonate, di(biphenyl-4-yl) carbonate, 4-(1-methyl-1-phenylethyl)phenylphenyl carbonate, di[4-(1-methyl-1-phenylethyl)phenyl] carbonate, bis(2-benzoylphenyl) carbonate, bis(phenylsalicylic) carbonate, and / or bis(benzylsalicylic) carbonate. At least one diaryl carbonate is particularly preferably diphenyl carbonate, 4-tert-butylphenylphenyl carbonate, di(4-tert-butylphenyl) carbonate, biphenyl-4-ylphenyl carbonate, di(biphenyl-4-yl) carbonate, 4-(1-methyl-1-phenylethyl)phenylphenyl carbonate, and / or di[4-(1-methyl-1-phenylethyl)phenyl] carbonate. At least one diaryl carbonate is particularly preferably diphenyl carbonate.

[0049] Furthermore, according to the present invention, at least one catalyst is present in step (i) of the method. This is preferably an inorganic base and / or an organic catalyst. The at least one catalyst is particularly preferably pK of 5 or less.b It is an inorganic or organic base that has [a certain characteristic].

[0050] At least one inorganic base or at least one organic catalyst is lithium, sodium, potassium, cesium, calcium, barium, and magnesium hydroxides, carbonates, halides, phenoxides, diphenoxides, fluorides, acetates, phosphates, hydrogen phosphates, and borates, tetramethylammonium hydroxide, tetramethylammonium acetate, tetramethylammonium fluoride, tetramethylammonium tetraphenylborate, tetraphenylphosphonium fluoride, tetraphenylphosphonium tetraphenylborate, dimethyldiphenylammonium hydroxide, tetraethylammonium hydroxide, cetyltrimethylammonium tetraphenylborate, cetyltrimethylammonium phenoxide, diazabicycloundecene (DBU), diazabicyclononene (DBN), 1,5,7-triazabicyclo[4.4.0] Deca-5-ene, 7-phenyl-1,5,7-triazabicyclo[4.4.0]deca-5-ene, 7-methyl-1,5,7-triazabicyclo[4.4.0]deca-5-ene, 7,7'-hexylidenedi-1,5,7-triazabicyclo[4.4.0]deca-5-ene, 7,7'-decylidenedi-1,5,7-triazabicyclo[4.4.0]deca-5-ene, 7,7'-dodecylidenedi-1,5,7-triazabicyclo[4.4 It is also preferable to select from the group consisting of [0]deca-5-ene, phosphazene base P1-t-oct(tert-octyliminotris(dimethylamino)phosphoran), phosphazene base P1-t-butyl(tert-butyliminotris(dimethylamino)phosphoran), and 2-tert-butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diaza-2-phosphoran (BEMP). Any desired mixture can also be used.

[0051] At least one catalyst is particularly preferably an organic base, preferably the above organic bases, very particularly preferably an alkylamine, imidazole (derivative), a guanidine base such as triazabicyclodecene, DMAP and its corresponding derivative, DBN, and DBU, most preferably DMAP. These catalysts offer a particular advantage in step (ii) of the method according to the present invention, that they can be separated and removed along with the chemical compounds desorbed during condensation, for example by reduced pressure. This means that the resulting polyester carbonate contains only a small amount of catalyst, or even none at all. This offers a particular advantage that the polymer does not contain inorganic salts, for example, phosgene, which are always formed in pathways where phosgene is used. Such salts are known to adversely affect the stability of polyester carbonates, because ions can act as catalysts with respect to the corresponding decomposition.

[0052] It is preferable to use at least one catalyst in an amount of 1 ppm to 5000 ppm, preferably 5 ppm to 1000 ppm, and particularly preferably 20 ppm to 200 ppm, per 1 mole of alicyclic dicarboxylic acid.

[0053] In another embodiment, the method according to the present invention is characterized in that the reaction in step (i) is carried out in the presence of at least one first catalyst and / or a second catalyst, and the condensation in step (ii) is carried out in the presence of at least the first catalyst and the second catalyst, wherein the first catalyst is at least one tertiary nitrogen base, the second catalyst is at least one basic compound, preferably a basic alkali metal salt, and the proportion of alkali metal cations in step (ii) is 0.0008% to 0.0050% by weight with respect to all components used in step (i).

[0054] Therefore, in this embodiment, the first catalyst and / or the second catalyst are present in step (i) of the method.

[0055] The first catalyst is a tertiary nitrogen base. This first catalyst is preferably selected from bases derived from guanidine, 4-dimethylaminopyridine (DMAP), 1,8-diazabicyclo[5.4.0]undeca-7-ene, 1,5-diazabicyclo[4.3.0]nona-5-ene, 1,5,7-triazabicyclo[4.4.0]deca-5-ene, hexamethylphosphorimide triamide, 1,2-dimethyl-1,4,5,6-tetrahydropyridine, 7-methyl-1,5,7-triazabicyclodeca-5-ene, 1,8-diazabicyclo[5.4.0]undeca-7-ene (DBU), DBN, ethylimidazole, N,N-diisopropylethylamine (Hünig base), pyridine, TMG, and mixtures of these substances. More preferably, the first catalyst is selected from a base derived from guanidine, 4-dimethylaminopyridine (DMAP), 1,8-diazabicyclo[5.4.0]undeca-7-ene, 1,5-diazabicyclo[4.3.0]nona-5-ene, and 1,5,7-triazabicyclo[4.4.0]deca-5-ene. The use of 4-dimethylaminopyridine is particularly preferred.

[0056] The first catalyst is preferably used in an amount of 0.002% to 0.10% by weight, more preferably 0.005% to 0.050% by weight, and particularly preferably 0.008% to 0.030% by weight, relative to all components used in step (i) of the method in each case.

[0057] The second catalyst is preferably selected from the group consisting of inorganic or organic alkali metal salts and inorganic or organic alkaline earth metal salts. More preferably, the alkali metal cations present in step (ii) are lithium cations, potassium cations, sodium cations, cesium cations, and mixtures thereof.

[0058] The second catalyst used is preferably an organic or inorganic alkali metal salt or alkaline earth metal salt of a weak acid (pKa between 3 and 7 at 25°C). Suitable weak acids include, for example, carboxylic acids, preferably C2-C2. 22 These include carboxylic acids, such as acetic acid, propionic acid, oleic acid, stearic acid, lauric acid, benzoic acid, 4-methoxybenzoic acid, 3-methylbenzoic acid, 4-tert-butylbenzoic acid, p-tolueneacetic acid, 4-hydroxybenzoic acid, salicylic acid, partial esters of polycarboxylic acids, such as monoesters of succinic acid, and branched aliphatic carboxylic acids, such as 2,2-dimethylpropanoic acid, 2,2-dimethylpropanoic acid, 2,2-dimethylbutanoic acid, and 2-ethylhexanoic acid. However, it is also possible to use organic or inorganic alkali metal salts or alkaline earth metal salts of strong acids, such as hydrochloric acid.

[0059] Suitable organic and inorganic salts include, or are derived from, sodium bicarbonate, potassium bicarbonate, lithium bicarbonate, sodium carbonate, lithium carbonate, potassium carbonate, sodium acetate, potassium acetate, lithium acetate, sodium stearate, potassium stearate, lithium stearate, sodium oleate, lithium oleate, potassium oleate, sodium benzoate, potassium benzoate, lithium benzoate, and disodium, dipotassium, and dilithium salts of BPA. Calcium bicarbonate, barium bicarbonate, magnesium bicarbonate, strontium bicarbonate, calcium carbonate, barium carbonate, magnesium carbonate, strontium carbonate, calcium acetate, barium acetate, magnesium acetate, strontium acetate, calcium stearate, barium stearate, magnesium stearate, and their corresponding oleates can also be used. Phenols, particularly their corresponding salts, can also be used. These salts can be used individually or in mixtures.

[0060] The second catalyst is preferably selected from the group consisting of sodium hydroxide, lithium hydroxide, sodium phenoxide, lithium phenoxide, sodium benzoate, lithium benzoate, lithium chloride, lithium acetylacetonate, and cesium carbonate, and mixtures thereof. Sodium phenoxide, lithium phenoxide, sodium hydroxide, lithium hydroxide, sodium benzoate, lithium benzoate, lithium chloride, and / or lithium acetylacetonate are particularly preferred. Lithium chloride is preferably used as an aqueous solution, for example, in the form of a 15% solution.

[0061] It was found that the molar ratio of all aliphatic dihydroxy compounds present in step (i) to all alicyclic dicarboxylic acids present in step (i) before the reaction in step (i) is preferably 1:0.6 to 1:0.05, more preferably 1:0.5 to 1:0.15, and very preferably 1:0.4 to 1:0.2.

[0062] To achieve particularly advantageous mechanical properties, good chemical resistance, and good processability, it is preferable that the ratio of aliphatic dihydroxy compounds to alicyclic dicarboxylic acids in the subsequent polyester carbonate is not too high (i.e., the content of incorporated alicyclic dicarboxylic acids is not too low). Polymers with a high content of units derived from dihydroxy compounds such as isosorbide are usually very rigid and therefore have insufficient mechanical properties. If the content of units derived from alicyclic dicarboxylic acids is too low, the processability of the resulting polymer will also be more insufficient. Furthermore, since polyester units generally provide good chemical resistance to polyester carbonates, the content of units derived from alicyclic dicarboxylic acids should not be too low either.

[0063] According to the present invention, the prepared polyester carbonate preferably has a relative solution viscosity η greater than 1.22, similarly preferably 1.25 to 1.65, particularly preferably 1.28 to 1.63, and very particularly preferably 1.30 to 1.62. Here, the relative solution viscosity is preferably measured at 25°C in dichloromethane at a concentration of 5 g / l using an Ubbelohde viscometer. Those skilled in the art are familiar with determining the relative solution viscosity using an Ubbelohde viscometer. According to the present invention, this determination is preferably carried out according to DIN 51562-3; 1985-05. This method involves measuring the flow time of the polyester carbonate to be measured using an Ubbelohde viscometer, and then confirming the difference in viscosity between the polymer solution and its solvent. For this purpose, the Ubbelohde viscometer is initially calibrated by measuring pure solvents, dichloromethane, trichloroethylene, and tetrachloroethylene (always at least 3 times, but at most 9 times). Next, the actual calibration is performed using dichloromethane as the solvent. Then, the polymer sample is weighed and dissolved in dichloromethane, and the flow time for this solution is determined three times. The relative solution viscosity is calculated by correcting the average of the flow times via the Hagenbach correction.

[0064] According to the present invention, these molar masses are preferably referred to as "sufficient" molar masses.

[0065] According to the present invention, a mixture of dihydroxy compounds is, in each case, a ratio of the sum of component (A) and component (B), Component (A) in an amount of 98 mol% to 75 mol%, preferably 97 mol% to 80 mol%, and particularly preferably 96 mol% to 82 mol%, Component (B) in an amount of 2 mol% to 25 mol%, preferably 3 mol% to 20 mol%, and particularly preferably 4 mol% to 18 mol%, It is particularly preferable that it contains [a specific compound]. According to the present invention, it has been found that the increase in molecular weight, and therefore surface renewal, is particularly good, especially within this range.

[0066] According to the present invention, in the method according to the present invention, 60 to 90 parts of isosorbide, preferably 65 to 85 parts of isosorbide or isosorbide isomer, 40 to 10 parts of alicyclic dicarboxylic acid, preferably 35 to 15 parts of alicyclic dicarboxylic acid, preferably 1,4-cyclohexanedicarboxylic acid, This is particularly advantageous in that case.

[0067] 2 mol% to 25 mol%, preferably 3 mol% to 20 mol%, and particularly preferably 4 mol% to 18 mol% of isosorbide is replaced by at least one further aliphatic diol, particularly a linear, very preferably branched diol having 2 to 10 carbon atoms. Here, the total amount of at least one aliphatic diol in the whole composition is preferably less than 20 mol%, and particularly less than 15 mol%.

[0068] The method according to the present invention is characterized by the release of carbon dioxide during the process. According to the present invention, carbon dioxide is preferably desorbed in step (i) of the method (see the reaction scheme above). This procedure enables a rapid reaction with low thermal stress.

[0069] Furthermore, step (i) of the present invention preferably includes at least one, and particularly preferably all, of the following steps (ia) to (ic):

[0070] (ia) A step of melting all components present in step (i), namely at least one alicyclic dicarboxylic acid, at least one diaryl carbonate, and at least components (A) and (B) in the presence of at least one catalyst. This is preferably carried out under a protective gas atmosphere, preferably under nitrogen and / or argon. Step (ia) is preferably carried out in the absence of a solvent. The term “solvent” is known to those skilled in the art in this context. According to the present invention, the term “solvent” is preferably understood to mean a compound that does not undergo a chemical reaction in either step (i) or step (ii). Compounds formed by the reaction (e.g., phenol when diphenyl carbonate is used as at least one diaryl carbonate) are excluded. Naturally, the presence of trace amounts of solvent in the starting compounds cannot be excluded. In this case, it is preferable to include them according to the present invention. However, according to the present invention, it is preferable to avoid an active step of adding such a solvent.

[0071] (ib) A step of heating the mixture, preferably the molten material obtained from step (ia). Steps (ia) and (ib) may overlap, since heating may be required in step (ia) to produce the molten material. The heating is preferably carried out initially at a temperature of 150°C to 180°C.

[0072] (ic) A step in which the mixture, preferably the mixture obtained from step (ib), is reacted, preferably by stirring, while introducing mixing energy. In this case, step (ic) may overlap with step (ib), because the reaction of the mixture may have already started due to heating. In this case, the molten material is preferably already heated to a temperature between 150°C and 180°C as a result of step (ib) under standard pressure. Depending on the catalyst selected, the temperature can be kept in the range of 160°C to 200°C. On the other hand, the temperature in step (ic) can be gradually increased to 200°C to 300°C, preferably 210°C to 260°C, and particularly preferably 215°C to 240°C, depending on the reactivity observed. The reactivity can be estimated from the generation of gas, as is known to those skilled in the art. In this step, higher temperatures are possible in principle, but higher temperatures may cause secondary reactions (e.g., discoloration). Therefore, higher temperatures are not very preferable. The mixture is stirred under standard pressure until the generation of gas has almost stopped. According to the present invention, under these conditions, it is also possible to partially remove the aryl alcohol (for example, phenol when using diphenyl carbonate) formed by the reaction of at least one carboxylic acid with at least one diaryl carbonate.

[0073] According to the present invention, it was also observed that at least one of the dihydroxy compounds (A) and / or (B) had similarly begun to react by this point. For example, oligomers containing carbonate units from the reaction of at least one of the dihydroxy compounds (A) and / or (B) with at least one diaryl carbonate and / or ester units from the reaction of at least one of the dihydroxy compounds (A) and / or (B) with at least one dicarboxylic acid could be detected.

[0074] Therefore, according to the present invention, it is preferable that, before carrying out step (ii), the mixture obtained from step (i) contains an oligomer comprising a carbonate unit from the reaction of at least one dihydroxy compound (component (A) and / or component (B)) with at least one diaryl carbonate and / or an ester unit from the reaction of at least one dihydroxy compound (component (A) and / or component (B)).

[0075] The reaction time in step (ic) depends on the amount of starting material. Preferably, the reaction time in step (ic) is between 0.5 hours and 24 hours, more preferably between 0.75 hours and 5 hours, and particularly preferably between 1 hour and 3 hours. In this case, it is preferable to select a reaction time such that gas generation almost subsides (see the reaction scheme above).

[0076] According to the present invention, the molar ratio of the total amount of all dihydroxy compounds and all alicyclic dicarboxylic acids present in method step (i) before the reaction in method step (i) to all diaryl carbonates present in method step (i) is preferably 1:0.4 to 1:1.6, more preferably 1:0.5 to 1:1.5, more preferably 1:0.6 to 1:1.4, particularly preferably 1:0.7 to 1:1.3, especially preferably 1:0.8 to 1:1.2, and very particularly preferably 1:0.9 to 1:1.1. Those skilled in the art can select the corresponding optimal ratio according to the purity of the starting materials.

[0077] Method step (ii) In step (ii), the mixture obtained from step (i) is subjected to further condensation while removing at least the chemical compounds eliminated during condensation. According to the present invention, the expression "further" condensation should be understood to mean that at least some condensation has already occurred in step (i). This is preferably a reaction between at least one alicyclic dicarboxylic acid and at least one diaryl carbonate, with the elimination of an aryl alcohol. However, it is also preferable that further condensation has already occurred to form an oligomer (see step (i) for this).

[0078] If only the first catalyst or only the second catalyst is used in step (i), the catalyst not used in step (i) is added in step (ii).

[0079] The proportion of alkali metal cations in step (ii) is preferably 0.0009% to 0.0005% by weight, and particularly preferably 0.0010% to 0.0045% by weight, relative to all components used in step (i) in each case.

[0080] In a preferred embodiment, the first catalyst and the second catalyst are present in step (i) of the method.

[0081] It is also possible to use a portion of the first catalyst and / or a portion of the second catalyst in step (i), and then use the remainder of each in step (ii).

[0082] However, it is preferable to use the total amount of the first catalyst and / or the second catalyst in method step (i). It is most preferable to use the total amount of both catalysts in method step (i).

[0083] The term "condensation" is known to those skilled in the art. This is understood to mean a reaction in which two molecules (of the same or different substances) combine to form a larger molecule, and a molecule of a chemically simpler substance is eliminated. This compound eliminated during condensation is removed in step (ii) of the method. Here, it is preferable to remove the chemical compound eliminated during condensation by reduced pressure in step (ii). Therefore, it is preferable that the method according to the present invention is characterized by optionally removing volatile components having a boiling point lower than the alicyclic diester formed in step (i), lower than the mixture of dihydroxy compounds, and lower than at least one diaryl carbonate, by stepwise reduced pressure during the reaction in step (i). When removing various volatile components, it is preferable to choose stepwise removal. It is also preferable to choose stepwise removal in order to remove the volatile components (there may be multiple) as completely as possible. The volatile components are the chemical compounds (there may be multiple) eliminated during condensation.

[0084] Stepwise depressurization can be performed, for example, by immediately reducing the pressure as the overhead temperature drops, thus ensuring the continuous removal of chemical compounds desorbed during condensation. Once a pressure of 1 mbar, preferably less than 1 mbar, is reached, condensation is continued until the desired viscosity is reached. This can be done, for example, by monitoring the torque; that is, stopping the polycondensation when the desired agitator torque is reached.

[0085] The condensation product is preferably removed in step (ii) at a temperature of 200°C to 280°C, particularly preferably 210°C to 260°C, and especially preferably 220°C to 250°C. The vacuum during removal is more preferably 500 mbar to 0.01 mbar. It is particularly preferable to remove the product in stages by lowering the vacuum. The vacuum in the final stage is very preferably 10 mbar to 0.01 mbar.

[0086] In further embodiments of the present invention, polyester carbonates obtained by the above-described methods of the present invention are provided in all disclosed combinations and preferred forms. The polyester carbonates of the present invention can be processed as is into all kinds of molded articles. They can also be processed together with other thermoplastics and / or polymer additives to obtain thermoplastic molding compounds. Molding compounds and molded articles are further subjects of the present invention.

[0087] The polymer additive is preferably selected from the group consisting of flame retardants, drip inhibitors, flame retardant aids, smoke suppressants, lubricants and mold release agents, nucleating agents, antistatic agents, conductive additives, stabilizers (e.g., hydrolysis stabilizers, heat aging stabilizers and UV stabilizers, and further anti-transesterification agents), flow promoters, compatibilizers, dyes and pigments, impact resistance modifiers, and further fillers and reinforcing agents.

[0088] Thermoplastic molding compounds can be prepared by known methods, for example, by mixing polyester carbonate and further components and performing melt compounding and melt extrusion in conventional units, such as internal kneaders, extruders, and twin-screw systems, preferably at a temperature of 200°C to 320°C. In the context of the present invention, this method is generally referred to as compounding.

[0089] Therefore, the term “molded compound” is understood to mean the product obtained when the components of a composition are melt-compounded and then melt-extruded.

[0090] Molded articles formed from polyester carbonate or a thermoplastic molding compound containing polyester carbonate according to the present invention can be manufactured, for example, by injection molding, extrusion, and blow molding. Another form of processing is the manufacture of molded articles by thermoforming from a pre-made sheet or film. [Modes for carrying out the invention] [Examples]

[0091] Materials used: Cyclohexanedicarboxylic acid: 1,4-cyclohexanedicarboxylic acid; CAS 1076-97-7 99%; Tokyo Chemical Industry Co., Ltd. (Japan), abbreviated as CHDA. Elemental analysis revealed that CHDA contained less than 1 ppm of sodium. Diphenyl carbonate: Diphenyl carbonate, 99.5%, CAS 102-09-0; Acros Organics (Hale, Belgium), abbreviated as DPC. 4-Dimethylaminopyridine: 4-Dimethylaminopyridine; 98.0% or more; purum; CAS 1122-58-3; Sigma-Aldrich (Munich, Germany), abbreviated as DMAP. Isosorbide: Isosorbide (CAS: 652-67-5), 99.8%, Polysorb PS A; Roquette Freres (France, Restrom 62136); abbreviated as ISB. Lithium hydroxide monohydrate (CAS: 1310-66-3); over 99.0%; Sigma-Aldrich. 2-Butyl-2-ethyl-1,3-propanediol: CAS number 115-84-4; Aldrich (abbreviated as BEPD). 2,2,4,4-Tetramethyl-1,3-cyclobutanediol:98% (CAS:3010-96-6); ABCR (abbreviated as TMCBD). 2,2,4-trimethyl-1,3-pentanediol; CAS number: 144-19-4; Aldrich (abbreviated as TMPD). Neopentyl glycol (2,2-dimethylpropane-1,3-diol); CAS: 126-30-7; Aldrich (abbreviated as NPG). 1,4-Butanediol: CAS: 110-63-4; Merck 99%; (abbreviated as BDO). 1,4-Cyclohexanedimethanol: CAS: 105-08-8, Aldrich 99% (abbreviated as CHDM). 1,12-Dodecanediol: CAS: 5675-51-4, Aldrich 99% (abbreviated as DDD).

[0092] Analysis method: solution viscosity Relative solution viscosity (η rel The relative viscosity (also known as relative η) was determined at 25°C in dichloromethane at a concentration of 5 g / l using an Ubbelohde viscometer. This determination was carried out according to DIN 51562-3; 1985-05. This method involves measuring the flow time of the polyester carbonate to be measured using an Ubbelohde viscometer, and then determining the difference in viscosity between the polymer solution and its solvent. To this end, the Ubbelohde viscometer is initially calibrated by measuring pure solvents, dichloromethane, trichloroethylene, and tetrachloroethylene (always at least 3 times, but no more than 9 measurements). Subsequently, the actual calibration is performed using the solvent dichloromethane. Next, the polymer sample is weighed and dissolved in dichloromethane, and the flow time of this solution is determined 3 times. The relative solution viscosity is calculated by correcting the average of the flow times via the Hagenbach correction.

[0093] Determination of glass transition temperature The glass transition temperature was determined by differential scanning calorimetry (DSC) under nitrogen at a heating rate of 10 K / min, in accordance with standards DIN EN ISO 11357-1:2009-10 and ISO 11357-2:2013-05. Here, the glass transition temperature (Tg) was determined as the inflection point during the second heating process.

[0094] MALDI-ToF-MS The sample was dissolved in chloroform. The matrix used was ditranol containing LiCl. The sample was analyzed in positive reflector mode and linear mode.

[0095] Comparative Example 1 (Experiment without using additional diols) First, 17.20 g (0.10 mol) of 1,4-cyclohexanedicarboxylic acid, 29.83 g (0.204 mol) of isosorbide, 64.30 g (0.3 mol) of diphenyl carbonate, 0.0111 g of DMAP (4-dimethylaminopyridine; 100 ppm relative to the starting materials CHDA, DPC, and ISB), and 115 μl of an aqueous solution of lithium hydroxide (100 g / l), equivalent to approximately 30 ppm of Li, were placed in a flask equipped with a short-pass separator. Oxygen was removed from the mixture by degassing and aeration with nitrogen four times. The mixture was melted and heated to 160°C at standard pressure with stirring. The mixture was stirred at 160°C for 40 minutes, 175°C for 60 minutes, 190°C for 30 minutes, and 205°C for 10 minutes. Carbon dioxide was continuously generated during this operation. Once CO2 generation ceased, the bath temperature was adjusted to 220°C. After another 20 minutes, a vacuum was applied. The pressure was reduced to 10 mbar over 30 minutes. During this process, phenol was continuously removed. The mixture was stirred at 10 mbar for approximately 10 minutes. Next, the pressure was reduced to less than 1 mbar (approximately 0.7 mbar), and condensation was continued for another 10 minutes. After that, the processing of the mixture was stopped.

[0096] A pale yellow polymer with a solution viscosity of 1.33 relative η was obtained.

[0097] Other examples (Ex.) and comparative examples (Comp.) were carried out as described for Comparative Example 1. First, unlike in Example 1, the aliphatic diols specified in Table 1 were placed together with all other monomers and catalysts that form the polymer in a flask equipped with a short-stroke separator.

[0098] [Table 1]

[0099] Examples 1 to 12 of the present invention demonstrate that, as long as the ratio of isosorbide to CHDA according to the present invention is observed, the desired polyester carbonate can be obtained with high viscosity by the method of the present invention. Here, it can be seen that the addition of further aliphatic diols, particularly branched diols, results in a significant increase in molecular weight compared to the example without further aliphatic diols (see Comparative Example 1). The observation of better miscibility at higher temperatures suggests that a further increase in molecular weight may have occurred. Furthermore, it is surprising that polymers with certain ISB + further aliphatic diol:CHDA ratios do not show a good increase in molecular weight. Comparative Example 2 shows that a higher proportion of cyclohexanedicarboxylic acid does not yield the desired polymer, and the resulting molecular weight is very low. Furthermore, this was not known from the literature / could not be inferred from the literature. Patent Document 12, which is an unpublished patent application, has already found that the ISB:CHDA ratio results in a good increase in molecular weight over a broad range defined by the present invention, but not outside this range. The addition of at least one further aliphatic diol results in a much larger increase in molecular weight, as can be seen from the comparison with Comparative Example 1 (see above).

[0100] Example 13 of the present invention: Reaction in step (i) of the method First, 0.10 mol of 1,4-cyclohexanedicarboxylic acid, 0.02 mol of BEPD (10%), 0.18 mol of isosorbide, 0.3 mol of diphenyl carbonate, 100 ppm of DMAP (4-dimethylaminopyridine; relative to the starting materials CHDA, BEPD, DPC, and ISB), and 0.0763 ml of aqueous lithium hydroxide solution (100 g / l), equivalent to approximately 20 ppm of Li, were placed in a flask equipped with a short-pass separator. Oxygen was removed from the mixture by four degassing and nitrogen aeration. The mixture was gradually heated to 190°C. Carbon dioxide was continuously generated during this operation. Next, a 3 ml sample was taken and analyzed by MALDI-ToF-MS. To ensure that the batch continued to polymerize, the reactants were heated to 220°C, and then the vacuum was gradually reduced to less than 1 mbar. An increase in viscosity was observed.

[0101] The results of the analysis are summarized in Table 2. The mass of each is Li adduct M + Li * This corresponds to the above. Various peaks were identified that may have already reacted with both ISB and BEPD. This clearly indicates that isosorbide and BEPD have already reacted under the method conditions of method step (i). In Table 2, ISB represents the isosorbide unit with two terminal OH groups removed (these are listed separately), CHDA represents cyclohexane (cyclohexanedicarboxylic acid with two carboxylic acid groups removed), and BEPD represents 2-butyl-2-ethyl-1,3-propanediol with two OH groups removed.

[0102] [Table 2]

[0103] These results suggest that the method of the present invention yields polyester carbonates different from those prepared via a two-step method (i.e., preparation of diaryl dicarboxylate by reaction of an alicyclic dicarboxylic acid with a diaryl carbonate and purification of the diaryl dicarboxylate, followed by condensation of the diaryl dicarboxylate with a diaryl carbonate and an aliphatic dihydroxy compound). It is very likely that various statistical distributions of carbonate units and / or ester units exist in various polyester carbonates.

Claims

1. A method for preparing polyester carbonate by molten transesterification, (i) A step of reacting at least one alicyclic dicarboxylic acid and at least one diaryl carbonate with at least one catalyst in the presence of a mixture of dihydroxy compounds comprising (A) at least one 1,4:3,6-dianhydrohexitol and (B) at least one further aliphatic dihydroxy compound, (ii) A step of further condensing the mixture obtained from step (i) while removing at least the chemical compounds that were removed during condensation, Includes, A method characterized in that the molar ratio of all dihydroxy compounds present in step (i) to all alicyclic dicarboxylic acids present in step (i) prior to the reaction in step (i) is 1:0.6 to 1:0.

05.

2. The aforementioned at least one further aliphatic dihydroxy compound has chemical formula (I): HO-X-OH (I) The method according to claim 1, characterized by having (wherein X represents a linear alkylene group having 2 to 22 carbon atoms that can be optionally interrupted by at least one heteroatom, a branched alkylene group having 4 to 20 carbon atoms that can be optionally interrupted by at least one heteroatom, or a cycloalkylene group having 4 to 20 carbon atoms that can be optionally interrupted by at least one heteroatom, wherein the cycloalkylene group may optionally contain a plurality of rings and may optionally be branched in each case).

3. The method according to claim 1 or 2, characterized in that the reaction in step (i) is carried out in the presence of at least one first catalyst and / or a second catalyst, and the condensation in step (ii) is carried out in the presence of at least the first catalyst and the second catalyst, wherein the first catalyst is at least one tertiary nitrogen base, the second catalyst is at least one basic compound, and the proportion of alkali metal cations in step (ii) is 0.0008% by weight to 0.0030% by weight with respect to all components used in step (i).

4. The at least one alicyclic dicarboxylic acid is of chemical formula (IIa), (IIb): 【Chemistry 1】 (In the formula, B is independent of CH ２ Represents a group, or a heteroatom selected from the group consisting of O and S. R １ Each of these independently represents an alkylene group having a single bond or 1 to 10 carbon atoms, and The method according to any one of claims 1 to 3, characterized in that n is selected from compounds or mixtures thereof (where n is a number between 0 and 3).

5. The method according to claim 3, characterized in that the first catalyst is selected from the group consisting of a base derived from guanidine, 4-dimethylaminopyridine, 1,8-diazabicyclo[5.4.0]undeca-7-ene (DBU), 1,5-diazabicyclo[4.3.0]nona-5-ene (DBN), 1,5,7-triazabicyclo[4.4.0]deca-5-ene, and mixtures thereof.

6. The method according to claim 3, characterized in that the at least one catalyst of claims 1 and 2 or the first catalyst of claim 3 is used in an amount of 0.002% to 0.1% by weight relative to all components used in step (i).

7. The method according to claim 3, characterized in that the second catalyst is selected from the group consisting of inorganic or organic alkali metal salts and inorganic or organic alkaline earth metal salts.

8. A polyester carbonate obtained by the method described in any one of claims 1 to 7.

9. A molded compound comprising the polyester carbonate described in claim 8.

10. A molded article comprising the polyester carbonate described in claim 8.

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