Patent Application
20230050973
The present invention relates to a method of separating a room temperature solid diisocyanate from a distillation residue that arises in a method for preparing the diisocyanate. The invention further provides the room temperature solid diisocyanate obtainable by this method. In addition, the invention further provides for the use of a thin-film evaporator and/or falling-film evaporator, a composition comprising the room temperature solid diisocyanate, and a method of producing an elastomer from this composition and the elastomer itself.
The industrial scale preparation of diisocyanates by reacting amines with phosgene in solvents is known and described in detail in the literature (Ullmanns Encyklopädie der technischen Chemie [Ullmann's Encyclopedia of Industrial Chemistry], 4th edition, volume 13, pages 347-357, Verlag Chemie, GmbH, D-6940 Weinheim, 1977 or else EP 1 575 908 A1). The purification of the diisocyanates prepared by these methods by distillation processes affords a distillation residue. Depending on the chemical nature of the diisocyanate prepared, this residue contains a considerable proportion of monomeric diisocyanate. The residue can be disposed of by incineration, but in that case the monomeric diisocyanate present therein is also lost.
Therefore, various methods have been developed for separating and recovering the monomeric diisocyanate present in the residue from the distillation residue. For this purpose, the residues are mixed with high-boiling hydrocarbons, for example bitumen, and then the diisocyanate present in the residue is separated in a kneader-drier, paddle drier or batchwise distillation method.
If the residue has a high viscosity extending as far as the solid state and the monomeric diisocyanates are not liquid at room temperature, the viscosity of the residue has to be lowered prior to any recovery in order to be able to perform a separation method at all. Heating of non-liquid residues does lower their viscosity, but there are also unwanted side reactions—for example oligomerizations—of the diisocyanate to be isolated. A further challenge in the recovery is that, in distillative methods, the bottoms output, i.e. the portion that remains from the diisocyanate separated, can also have a high viscosity and can therefore be removed from the separation apparatus only with difficulty. In conventional recovery methods, this high viscosity frequently results from oligomerizations of diisocyanate still present in the bottoms output that have been caused by high temperatures.
Naphthalene diisocyanate (NDI) has found broad industrial use and can be prepared by known methods described at the outset, for example phosgenation, from naphthalenediamine (NDA). Since monomeric naphthalene diisocyanate is a solid, the purification of the product fundamentally constitutes a challenge compared to other isocyanates that are liquid at processing temperature, for example tolylene diisocyanate (TDI). The difficulties are further increased by the physical properties of naphthalene diisocyanate because it melts at 127° C. and already begins to sublime at 130° C. The residue from the process for purifying naphthalene diisocyanate still contains about 70-80% by weight of monomeric naphthalene diisocyanate. 150 to 300 tonnes per year of naphthalene diisocyanate present in the residue from the purification method are incinerated. The recovery of monomeric naphthalene diisocyanate in a batchwise distillation method recovers about 50% of the monomeric naphthalene diisocyanate present in the residue. Typically, the residue in this process has to be dissolved in about 30% by weight of bitumen, which has to be provided specially from mineral oil and hence leads to an unwanted waste burden and hence pollution of the environment, since it is incinerated with the remaining residue.
U.S. Pat. No. 3,694,323 discloses a method of recovering an isocyanate from a residue with the aid of a further isocyanate which has a higher boiling point than the isocyanate to be purified and hence lowers the viscosity of the residue and enables purification. The document also makes general mention of naphthalene diisocyanate in a long list, but discloses only tolylene diisocyanate in the experimental part and does not contain any teaching as to the particular difficulties in the recovery of a room temperature solid diisocyanate. Another disadvantage of this method is that the method has a comparatively high energy requirement since temperatures between 190° C. and 250° C. are required in the examples for the purification of TDI.
A disadvantage of the conventional methods of recovering diisocyanate from the distillation residue is the use of relatively large amounts of an additive that can contaminate the recovered diisocyanate. In addition, the performance of most conventional methods at high temperatures of more than 180° C. requires a large amount of energy. Moreover, these temperatures lead to unwanted oligomerization reactions of the monomeric diisocyanate.
There is therefore a need for a method for the recovery of diisocyanates, especially of room temperature solid diisocyanates such as naphthalene diisocyanate, from distillation residues that are obtained in the preparation of diisocyanates, in which an at least the same or a higher proportion of the diisocyanate present in the residue can be recovered than in conventional methods, and which simultaneously consumes a lower level of energy and additives. Additionally advantageous are methods that can be performed as a continuous process. In addition, the diisocyanate recovered was to be very substantially free of extraneous materials, for example additives from the recovery process.
It was therefore an object of the present invention to provide a method of recovering room temperature solid diisocyanates, especially naphthalene diisocyanate, from a distillation residue, by which at least an equal or even a higher proportion of the diisocyanate present in the residue, especially of naphthalene diisocyanate, can be recovered than by conventional methods. At the same time, the method of the invention is to consume less energy and a lower level of additives than conventional methods. Furthermore, the diisocyanate recovered is to be very substantially free of extraneous materials, for example additives from the recovery process, such that it can be used without further purification processes as reactant for further syntheses, for example polymer syntheses.
This object was achieved by a method of separating a room temperature solid diisocyanate from a distillation residue from a method for preparing the diisocyanate, comprising the following steps:
It has now been found that, surprisingly, even room temperature solid diisocyanates can be recovered in good yield from a distillation residue when polyisocyanates formed from diisocyanates other than the room temperature solid diisocyanate and having low residual monomer contents are added, and the addition of bitumen is unnecessary. Nevertheless, it is possible to keep the mixture of the residue liquid throughout the distillation process. Furthermore, the recovered diisocyanate has a very low level of impurities. Moreover, the method of the invention enables an efficient mode of production since it is possible to react to varying load by correspondingly varying the polyisocyanate added to the distillation residue.
The references to “comprising”, “containing”, etc., preferably denote “substantially consisting of” and very particularly preferably denote “consisting of”. The further embodiments identified in the claims and in the description can be combined arbitrarily, provided the context does not clearly indicate that the opposite is the case.
In the present context, “room temperature solid diisocyanates” is understood to mean that the diisocyanates are in the solid state of matter at 23° C. and standard pressure, i.e. 1000 mbar.
In the present context, naphthalene diisocyanate is understood as an umbrella term for the possible isomers or mixtures thereof. Examples of such isomers are naphthalene 1,5-diisocyanate or naphthalene 1,8-diisocyanate.
In the present context, what is meant by “at least one polyisocyanate based on one or more diisocyanates other than the diisocyanate which is solid at room temperature” is that this is not a monomeric diisocyanate and that no room temperature solid diisocyanates are used in the production thereof.
Suitable thin-film evaporators are, for example, rigid blade rotor thin-film evaporators or wiper-blade thin-film evaporators or short-path evaporators.
Suitable falling-film evaporators are, for example, shell and tube downpipe evaporators or helical tube evaporators.
In a first preferred embodiment, the at least one polyisocyanate in step (i) has a residual monomer content of ≤1.5% by weight, preferably of ≤1.0% by weight and more preferably of ≤0.5% by weight, determined by gas chromatography with an internal standard to DIN EN ISO 10283:2007-11. In this way, it is possible to further increase the yield and/or purity of recovered room temperature solid diisocyanate. Even though it is not absolutely necessary for any residues of monomeric diisocyanates to be present at all, it may be particularly preferable when the residual monomer content of the at least one polyisocyanate is >0.15% by weight. This results in the further advantage that the efficiency of production plants can be improved further since polyisocyanate that does not meet the desired specifications can still be used for the recovery from the distillation residue.
The distillation residue in step (i) preferably contains from 30% to 70% by weight of the room temperature solid diisocyanate, more preferably 40% to 60% by weight, especially preferably 45% to 55% by weight, based in each case on the distillation residue.
Furthermore, the distillation residue is preferably low in solvent. This means that, based on its weight, it contains preferably not more than 20% by weight, more preferably not more than 10% by weight and most preferably not more than 5% by weight of one or more organic solvents. What is meant here by organic solvent is compounds that do not contain any isocyanate groups. Organic solvents are especially understood to mean the compounds described further down in this application in the context of the phosgenation of amines.
In a further preferred embodiment, in step (i), 85% to 75% by weight of the distillation residue is mixed with 15% to 25% by weight of the at least one polyisocyanate, and preferably 85% to 80% by weight of the distillation residue with 15% to 20% by weight of the at least one polyisocyanate, based in each case on the sum total of the masses of the distillation residue and the at least one polyisocyanate. This results in the additional advantage that process economy can be further increased.
In a further preferred embodiment, the room temperature solid diisocyanate is naphthalene 1,5-diisocyanate, naphthalene 1,8-diisocyanate, phenylene 1,4-diisocyanate, tetralin diisocyanate, o-toluidine diisocyanate, durene diisocyanate, benzidine diisocyanate and/or anthrylene 1,4-diisocyanate, more preferably naphthalene 1,5-diisocyanate, naphthalene 1,8-diisocyanate, phenylene 1,4-diisocyanate, tetralin diisocyanate and/or o-toluidine diisocyanate and more preferably naphthalene 1,5-diisocyanate and/or naphthalene 1,8-diisocyanate.
In principle, the room temperature solid diisocyanates can be prepared by any routes, for example by reaction of the corresponding diamines or salts thereof with phosgene. All that is important in each case is that the method utilized leaves at least one distillation residue containing room temperature solid diisocyanates that can then be used in step (i) of the invention.
It is particularly preferable that the method for preparing the diisocyanate is a phosgenation of a diamine, more preferably a liquid phase phosgenation of a diamine.
Preferably, in the process for preparation of the diisocyanate, a diamine that has the structure of the diisocyanate apart from the isocyanate groups is used, but in which the two amino groups have been exchanged for isocyanate groups in the preparation process. By way of example, naphthalene 1,5-diamine is the corresponding diamine of naphthalene 1,5-diisocyanate. When the room temperature solid diisocyanate is an isomer mixture, a corresponding isomer mixture of diamines is used.
The continuous preparation of organic isocyanates by reaction of primary organic amines with phosgene has been described many times, and is conducted on an industrial scale. Particular preference is given to preparing the room temperature solid diisocyanate from the corresponding diamine using phosgene by the method known from WO 2014/044699 A1, which comprises the following steps:
(A) preparing a suspension of the corresponding diamine in an inert solvent, where the diamine is distributed in the solvent by means of a dynamic mixing unit,
(B) phosgenating the diamine suspended in the inert solvent to obtain the respective diisocyanate,
wherein the dynamic mixing unit in step (A) is selected from the group consisting of dispersing disks and rotor-stator systems, preferably rotor-stator systems, more preferably colloid mills, toothed dispersing machines and three-roll mills. Very particular preference is given to toothed dispersing machines as dynamic mixing units.
The dispersing disks and rotor-stator systems mentioned in the above paragraph have the same meaning as at page 4 line 17 to page 5 line 11 of WO 2014/044699 A1.
Suitable inert solvents are aromatic solvents, which may also be halogenated. Examples of these are toluene, monochlorobenzene, o-, m- or p-dichlorobenzene, trichlorobenzene, chlorotoluenes, chloroxylenes, chloroethylbenzene, chloronaphthalenes, chlorodiphenyls, xylenes, decahydronaphthalene, benzene or mixtures of the above solvents. Further examples of suitable organic solvents are methylene chloride, perchloroethylene, hexane, diethyl isophthalate, tetrahydrofuran (THF), dioxane, trichlorofluoromethane, butyl acetate and dimethylformamide (DMF). Preference is given to using monochlorobenzene or o-dichlorobenzene or a mixture of the two; particular preference is given to using monochlorobenzene.
Phosgene is used in excess in the reaction in step (B). This means that more than one mole of phosgene is used per mole of amine groups. The molar ratio of phosgene to amine groups is accordingly from 1.01:1 to 20:1, preferably 1.1:1 to 10:1, more preferably 1.1:1 to 5.0:1. If necessary, further phosgene or phosgene solution can be supplied to the reaction mixture during the reaction in order to maintain a sufficient excess of phosgene or to compensate for loss of phosgene.
The reaction can be performed continuously and batchwise. Useful reactors include stirred tanks, tubular reactors, spray towers or else loop reactors. In principle, it is alternatively possible to utilize other designs that are not listed here by way of example. Preference is given to batchwise operation.
The reaction can be conducted until complete conversion to the isocyanate within the first reaction stage. Alternatively, it may be advantageous or necessary to conduct a partial conversion, especially of residues of amine hydrochloride, in a downstream reactor. The downstream reactor may comprise customary reactor designs with different degrees of backmixing, such as stirred tanks, loop reactors or tubular reactors. It may also be advantageous to divide the reaction mixture into substreams according to its particle size distribution and feed them separately to one or more downstream reactors. Useful designs for the removal include known apparatuses such as filters, cyclones or gravitational separators, for example. The substreams may be treated before or during the reaction by appropriate mechanical methods of adjusting the particle size, for example by grinding.
The unconverted phosgene is usually recycled, optionally after purification, and reused for phosgenation.
Methods available for separating the diisocyanate from the solvent include those known to the person skilled in the art, for example crystallization, sublimation or distillation, optionally with addition of seed crystals or azeotroping agents, for example. Preference is given to using a method comprising crystallization or distillation. The above mentioned methods leave a highly viscous or even solid residue that contains a variably high proportion of diisocyanates. It is possible with preference to use residues from the methods of crystallization and sublimation as distillation residue for the method of the invention.
In a further preferred embodiment, the residue has an average residence time in the treatment in step (ii) of ≥1 to ≤15 minutes, preferably of ≥1 to ≤10 minutes and more preferably of ≥1 to ≤5 minutes in the at least one thin-film evaporator and/or falling-film evaporator; more preferably, the residue has this residence time in a conventional glass falling-film evaporator having an evaporator area of 0.1 m2 (diameter 100 mm, length 300 mm) This results in the advantage that the likelihood of unwanted side reactions—for example oligomerizations—can be reduced further.
Step (ii) of the method is preferably performed at a temperature of 130° C. to 180° C. and a pressure of 0.4 to 4 mbar, preferably from 140° C. to 170° C. and from 0.6 mbar to 2 mbar, more preferably from 150° C. to 160° C. and from 0.7 to 1.5 mbar. This results in the advantage that the formation of by-products, i.e. oligomerization of the diisocyanate and of the polyisocyanate mixed in during the distillation, can be very substantially suppressed.
Preferably, the bottoms output from step (ii) is not in solid form at the prevailing temperature at the outlet from the thin-film evaporator and/or falling-film evaporator. Preferably, the bottoms output is discharged continuously from the distillation apparatus and then either recycled, for example by incineration to obtain heat, or discarded. More preferably, the bottoms output is liquid under the distillation conditions.
In a further preferred embodiment, a coolant is used in the distillation in step (iii), wherein the coolant temperature is preferably below the melting point of the room temperature solid diisocyanate. The coolant serves for rapid condensation of the product stream.
The solid material from step (iii) preferably contains at least 95% by weight of the room temperature solid diisocyanate, more preferably at least 97% by weight, especially preferably at least 99% by weight, based in each case on the solid material. Preferably, the proportion of solid diisocyanate in the solid material is determined by gas chromatography methods. The reduced use of auxiliaries such as bitumen in step (i) of the method minimizes the contamination of the monomeric room temperature solid diisocyanate obtained from the residue.
Polyisocyanates suitable for the process of the invention in step (i) are any polyisocyanates preferably having a uretdione, isocyanurate, allophanate, biuret, iminooxadiazinedione and/or oxadiazinetrione structure that are produced through modification of simple aliphatic, cycloaliphatic, araliphatic and/or aromatic diisocyanates, for example those of the type specified below, as described by way of example in J. Prakt. Chem. 336 (1994) 185-200, in DE-A 1 670 666, DE-A 1 954 093, DE-A 2 414 413, DE-A 2 452 532, DE-A 2 641 380, DE-A 3 700 209, DE-A 3 900 053 and DE-A 3 928 503 or in EP-A 0 336 205, EP-A 0 339 396 and EP-A 0 798 299, and any desired mixtures of such polyisocyanates. In addition to or as an alternative to the structures specified above with preference, it is also possible to use a polyisocyanate having urethane structure which can be prepared by known methods by reaction of simple aliphatic, cycloaliphatic, araliphatic and/or aromatic diisocyanates, for example those of the type specified below, with polyols having a molecular weight of 168 to 4000 g/mol, preferably at least trimethylolpropane and/or diethylene glycol, and any mixtures of such polyisocyanates. Thus, the polyisocyanates suitable for step (i) are oligomeric polyisocyanates containing at least one structure selected from the group consisting of urethane, uretdione, isocyanurate, allophanate, biuret, iminooxadiazinedione and oxadiazinetrione structures. Polyisocyanates containing no such structure, i.e. unmodified polyisocyanates, are referred to in this application as monomeric poly- or diisocyanates.
In the production of these polyisocyanates, the actual modification reaction is generally followed by a further process step for removing the unreacted excess monomeric diisocyanates. This removal of monomers is effected by processes known per se, preferably by thin-film distillation under reduced pressure or by extraction with suitable solvents inert toward isocyanate groups, for example aliphatic or cycloaliphatic hydrocarbons such as pentane, hexane, heptane, cyclopentane or cyclohexane.
However, it is essential to the invention that the polyisocyanates have a content of monomeric diisocyanates as defined above of ≤3.0% by weight, preferably of ≤2.5% by weight, more preferably of ≤2.0% by weight, even more preferably of ≤1.5% by weight, especially preferably of ≤1.0% by weight and most preferably of ≤0.5% by weight, determined by gas chromatography with internal standard according to DIN EN ISO 10283:2007-11. Even though it is not absolutely necessary for residues of monomeric diisocyanates to be present at all, it may be particularly preferable when the residual monomer content of the at least one polyisocyanate is >0.15% by weight and ≤3.0% by weight, preferably >0.15% by weight and ≤1.5% by weight, more preferably >0.15% by weight and ≤1.0% by weight and most preferably >0.15% by weight and ≤0.5% by weight. This results in the further advantage that the efficiency of production plants can be improved further since polyisocyanate that does not meet the desired specifications can still be used for the recovery from the distillation residue.
The polyisocyanates specified above as suitable, preferred, particularly preferred and especially preferred preferably contain isocyanurate structures and have an average NCO functionality of 2.3 to 5.0, preferably of 2.5 to 4.5, and a content of isocyanate groups of 6.0 to 26.0% by weight, preferably of 8.0 to 25.0% by weight, particularly preferably 10.0 to 24.0% by weight.
Suitable diisocyanates for preparation of the polyisocyanates are any diisocyanates obtainable in various ways, for example by phosgenation in the liquid or gas phase or by a phosgene-free route, for example by thermal urethane cleavage. Preferred diisocyanates are those from the molecular weight range of 140 to 400 having aliphatically, cycloaliphatically, araliphatically and/or aromatically bonded isocyanate groups, examples being 1,4-diisocyanatobutane, 1,5-diisocyanatopentane (PDI), 1,6-diisocyanatohexane (HDI), 2-methyl-1,5-diisocyanatopentane, 1,5-diisocyanato-2,2-dimethylpentane, 2,2,4- or 2,4,4-trimethyl-1,6-diisocyanatohexane, 1,10-diisocyanatodecane, 1,3- and 1,4-diisocyanatocyclohexane, 1,3- and 1,4-bis(isocyanatomethyl)cyclohexane, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane (isophorone diisocyanate, IPDI), m-xylylene diisocyanate (m-XDI), 4,4′-diisocyanatodicyclohexylmethane, 1-isocyanato-1-methyl-4(3)isocyanatomethylcyclohexane, bis(isocyanatomethyl)norbornane (NBDI), 1,3- and 1,4-bis(2-isocyanatoprop-2-yl)benzene (TMXDI), 2,4- and 2,6-diisocyanatotoluene (TDI), 2,4′- and 4,4′-diisocyanatodiphenylmethane (MDI) or any mixtures of such diisocyanates.
More preferably, the at least one polyisocyanate in step (i) is a polyisocyanate obtainable by modification of simple aliphatic, cycloaliphatic, araliphatic and/or aromatic diisocyanates, preferably by modification of 1,5-diisocyanatopentane (PDI), 1,6-diisocyanatohexane (HDI), 1,3- and 1,4-bis(isocyanatomethyl)cyclohexane, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane (isophorone diisocyanate, IPDI), m-xylylene diisocyanate (m-XDI), 4,4′-diisocyanatodicyclohexylmethane, bis(isocyanatomethyl)norbornane (NBDI), 2,4- and 2,6-diisocyanatotoluene (TDI) and/or 2,4′- and 4,4′-diisocyanatodiphenylmethane (MDI) and most preferably by modification of 1,5-diisocyanatopentane (PDI), 1,6-diisocyanatohexane (HDI), 1,3- and 1,4-bis(isocyanatomethyl)cyclohexane, 1-isocyanato-3,3,5-trimethyl-5-isocyanatomethylcyclohexane (isophorone diisocyanate, IPDI), m-xylylene diisocyanate (m-XDI), 4,4′-diisocyanatodicyclohexylmethane, bis(isocyanatomethyl)norbornane (NBDI) and/or 2,4- and 2,6-diisocyanatotoluene (TDI).
It is a great advantage of the method of the invention that the addition of bitumen that has been necessary to date in the recovery of room temperature solid diisocyanates from distillation residues is no longer required, and the mixture can be kept liquid throughout the distillation process. If any, in step (i), less than 5% by weight of bitumen, preferably less than 2% by weight and more preferably 0% by weight of bitumen, based on the mass of the distillation residue, is present. Bitumen and the production thereof are known to the person skilled in the art.
In a further preferred embodiment, the residue used in the method of the invention contains ≥0% by weight to ≤4% by weight, preferably ≥0.001% by weight to ≤2% by weight and more preferably ≥0.01% by weight to ≤1% by weight, based in each case on the total amount of the residue containing room temperature solid diisocyanates, of monomeric diisocyanates that have a boiling temperature above the boiling temperature of the room temperature solid diisocyanate and are different therefrom. This is particularly advantageous since, even without this addition, a high yield can be achieved in the recovery and the purified room temperature solid diisocyanate thus remains very substantially free of these impurities.
The percentages by weight of monomeric diisocyanates having a boiling temperature above the boiling temperature of the room temperature solid diisocyanate are determined by gas chromatography by means of an FID detector, preferably using an Optima 5 column and the following parameters: split rate: 8.31:1 mL/min; flow rate: 96.4 mL/min; pressure: 0.7 bar, carrier gas: helium, injection volume: 1 μL, inliner: straight split liner filled with Carbofritt, equating the area percentage with the percentage by weight in the evaluation.
A further embodiment of the invention relates to the use of a mixture containing 70% to 90% by weight of a distillation residue from a process for preparing a room temperature solid diisocyanate and 10% to 30% by weight of at least one polyisocyanate based on one or more diisocyanates other than the room temperature solid diisocyanate, based in each case on the mixture, in a method of separating off the room temperature solid diisocyanate by distillation by means of a thin-film evaporator and/or falling-film evaporator.
Preferably, the solid material containing the room temperature solid diisocyanate from step (iii) of the method, alone or else in mixtures with a diisocyanate obtained directly from the first purification stage after the phosgenation reaction, can be sent to all end uses familiar to the person skilled in the art. In one embodiment, the solid material is used for production of high-performance elastomers, for example Vulkollan®. Especially preferred is the further processing of the solid material with NCO-reactive compounds such as polyols to give polyurethanes, optionally via prepolymers as intermediates.
A further embodiment of the invention relates to a composition comprising a solid material comprising a room temperature solid diisocyanate from step (iii) of a method as claimed in any of claims 1 to 9 and at least one NCO-reactive compound, preferably at least one polyesterpolyol.
The present invention further provides a method of producing an elastomer, in which at least one composition of the invention is chemically reacted, optionally while heating, and the elastomer produced or producible by this method.
These elastomers are preferably polyurethanes that are optionally obtained via prepolymers as intermediates.
These polyurethanes preferably have apparent densities of 200 kg/m3 to 1400 kg/m3, more preferably of 600 kg/m3 to 1400 kg/m3 and most preferably of 800 kg/m3 to 1400 kg/m3. Very particular preference is given to producing cellular or bulk cast elastomers, more preferably polyester polyol-based cast elastomers.
The above-described composition may preferably comprise customary auxiliaries and additives, for example rheology improvers (for example ethylene carbonate, propylene carbonate, dibasic esters, citric esters), stabilizers (for example Bronsted and Lewis acids, for instance hydrochloric acid, phosphoric acid, benzoyl chloride, organo mineral acids such as dibutyl phosphate, and also adipic acid, malic acid, succinic acid, pyruvic acid or citric acid), UV stabilizers (for example 2,6-dibutyl-4-methylphenol), hydrolysis stabilizers (for example sterically hindered carbodiimides), emulsifiers and catalysts (for example trialkylamines, diazabicyclooctane, tin dioctoate, dibutyltin dilaurate, N-alkylmorpholine, lead octoate, zinc octoate, tin octoate, calcium octoate, magnesium octoate, the corresponding naphthenates and p-nitrophenoxide and/or else mercury phenylneodecanoate) and fillers (for example chalk), dyes which may be incorporable into the polyurethane/polyurea to be formed at a later stage (which thus possess Zerewitinoff-active hydrogen atoms) and/or color pigments.
NCO-reactive compounds used may be any compounds known to those skilled in the art.
Preferred NCO-reactive compounds are polyether polyols, polyester polyols, polycarbonate polyols and polyether amines having an average OH or NH functionality of at least 1.5, and short-chain polyols and polyamines (chain extenders or crosslinkers), as are sufficiently well known from the prior art. These may be, for example, low molecular weight diols (e.g. ethane-1,2-diol, propane-1,3- or -1,2-diol, butane-1,4-diol), triols (e.g. glycerol, trimethylolpropane) and tetraols (e.g. pentaerythritol), but also higher molecular weight polyhydroxyl compounds such as polyether polyols, polyester polyols, polycarbonate polyols, polysiloxane polyols, polyamines and polyether polyamines and polybutadiene polyols.
Polyether polyols are obtainable in a manner known per se by alkoxylation of suitable starter molecules under base catalysis or by the use of double metal cyanide compounds (DMC compounds). Examples of suitable starter molecules for the preparation of polyether polyols are simple low molecular weight polyols, water, organic polyamines having at least two N—H bonds, or any mixtures of such starter molecules. Preferred starter molecules for preparation of polyether polyols by alkoxylation, especially by the DMC method, are especially simple polyols such as ethylene glycol, propylene 1,3-glycol and butane-1,4-diol, hexane-1,6-diol, neopentyl glycol, 2-ethylhexane-1,3-diol, glycerol, trimethylolpropane, pentaerythritol, and low molecular weight hydroxyl-containing esters of such polyols with dicarboxylic acids of the kind specified hereinafter by way of example, or low molecular weight ethoxylation or propoxylation products of such simple polyols, or any desired mixtures of such modified or unmodified alcohols. Alkylene oxides suitable for the alkoxylation are in particular ethylene oxide and/or propylene oxide, which may be used in the alkoxylation in any desired order or also in a mixture.
Polyester polyols can be prepared in a known manner by polycondensation of low molecular weight polycarboxylic acid derivatives, for example succinic acid, adipic acid, suberic acid, azelaic acid, sebacic acid, dodecanedioic acid, tetrahydrophthalic anhydride, hexahydrophthalic anhydride, tetrachlorophthalic anhydride, endomethylenetetrahydrophthalic anhydride, glutaric anhydride, maleic acid, maleic anhydride, fumaric acid, dimer fatty acid, trimer fatty acid, phthalic acid, phthalic anhydride, isophthalic acid, terephthalic acid, citric acid or trimellitic acid, with low molecular weight polyols, for example ethylene glycol, diethylene glycol, neopentyl glycol, hexanediol, butanediol, propylene glycol, glycerol, trimethylolpropane, 1,4-hydroxymethylcyclohexane, 2-methylpropane-1,3-diol, butane-1,2,4-triol, triethylene glycol, tetraethylene glycol, polyethylene glycol, dipropylene glycol, polypropylene glycol, dibutylene glycol and polybutylene glycol, or by ring-opening polymerization of cyclic carboxylic esters such as ε-caprolactone. In addition, it is also possible to polycondense hydroxycarboxylic acid derivatives, for example lactic acid, cinnamic acid or ω-hydroxycaproic acid to give polyester polyols. However, it is also possible to use polyester polyols of oleochemical origin. Such polyester polyols can be prepared, for example, by full ring-opening of epoxidized triglycerides of an at least partly olefinically unsaturated fatty acid-containing fat mixture with one or more alcohols having 1 to 12 carbon atoms and subsequent partial transesterification of the triglyceride derivatives to alkyl ester polyols having 1 to 12 carbon atoms in the alkyl radical.
The NCO-reactive compound may contain short-chain polyols or polyamines as crosslinker component or chain extender. Typical chain extenders are diethylenetoluenediamine (DETDA), 4,4′-methylenebis(2,6-diethyl)aniline (MDEA), 4,4′-methylenebis(2,6-diisopropyl)aniline (MDIPA), 4,4′-methylenebis(3-chloro-2,6-diethyl)aniline (MCDEA), dimethylthiotoluenediamine (DMTDA, Ethacure® 300), N,N′-di(sec-butyl)aminobiphenylmethane (DBMDA, Unilink® 4200) or N,N′-di-sec-butyl-p-phenylenediamine (Unilink® 4100), 3,3′-dichloro-4,4′-diaminodiphenylmethane (MBOCA), trimethylene glycol di-p-aminobenzoate (Polacure 740M). Aliphatic aminic chain extenders can likewise be used or used in part. Propane-1,3-diol, butane-1,4-diol, butane-2,3-diol, pentane-1,5-diol, hexane-1,6-diol and HQEE (hydroquinone di(β-hydroxyethyl)ether), and also water. Very particular preference is given to using butane-1,4-diol for bulk cast elastomers and water for cellular cast elastomers.
An overview of polyurethanes and their properties and uses is given, for example, in the Kunststoffhandbuch [Plastics Handbook], volume 7, Polyurethane [Polyurethanes], 3rd newly revised edition, volume 193, edited by Prof. Dr. G. W. Becker and Prof. Dr. D. Braun (Carl-Hanser-Verlag, Munich, Vienna).
Preference is given to using NCO-terminated prepolymers having an NCO content of 2% to 15% by weight, very particularly of 2-10% by weight. The room temperature solid diisocyanate is preferably reacted with polyols of functionality 2 to 3, preferably 2, and an OH number of 28-112 mg KOH/g of substance to give prepolymers. Preference is given to using ester-based polyols. The NCO prepolymers thus prepared are either converted further directly or stored as storage-stable prepolymers in drums, for example, until they are ultimately used. Preference is given to using 1,5-NDI-based prepolymers. The production of the cast elastomers (molded articles) is advantageously conducted at an NCO/OH ratio of 0.7 to 1.30. In the case of cellular elastomers, the amount of the mixture introduced into the mold is typically such that the shaped bodies obtained have the density already described. The starting components are typically introduced into the mold at a temperature of 30 to 110° C. The degrees of densification are between 1.1 and 8, preferably between 2 and 6. The cellular elastomers are appropriately produced by a low-pressure technique or especially the reaction injection molding technique (RIM) in open molds, preferably closed molds. The reaction injection molding methodology is common knowledge to the person skilled in the art.
Additives such as castor oil or carbodiimides (for example Stabaxols from Rheinchemie as hydrolysis stabilizer, 2,2′,6,6′-tetraisopropyldiphenylcarbodiimide is a known representative) can be added either to the polyol or to the prepolymer. Water, emulsifiers, catalysts and/or auxiliaries and/or additives commonly form the polyol component together with the polyol.
For better demolding, it is customary to provide the molds with external separating agents, for example wax- or silicone-based compounds or aqueous soap solutions. The demolded shaped bodies are typically subjected to subsequent heat treatment at temperatures of 70 to 120° C. for 1 to 48 hours.
Emulsifiers used are, for example, sulfonated fatty acids and further commonly known emulsifiers, for example polyglycol esters of fatty acids, alkylaryl polyglycol ethers, alkoxylates of fatty acids, preferably polyethylene glycol esters, polypropylene glycol esters, polyethylene-polypropylene glycol esters, ethoxylates and/or propoxylates of linoleic acid, linolenic acid, oleic acid, arachidonic acid, more preferably oleic acid ethoxylates. Alternatively, it is also possible to use polysiloxanes. Salts of fatty acids with amines, e.g. diethylamine oleate, diethanolamine stearate, diethanolamine ricinoleate, salts of sulfonic acids, e.g. alkali metal or ammonium salts of dodecylbenzene- or dinaphthylmethanedisulfonic acid, are likewise preferred.
The sulfonated fatty acids can preferably be used as aqueous solutions, for example as a 50% solution. Typical known products are SV and SM additives from Rheinchemie, and WM additive from Rheinchemie as a nonaqueous emulsifier.
The method of producing the cellular PUR cast elastomers is conducted in the presence of water. The water acts both as crosslinker with formation of urea groups and as blowing agent on account of the reaction with isocyanate groups to form carbon dioxide. The amounts of water that can appropriately be used are 0.01% to 5% by weight, preferably 0.3% to 3.0% by weight, based on the weight of the polyol component. The water may be used entirely or partly in the form of the aqueous solutions of the sulfonated fatty acids.
The catalysts may be added individually or else in a blend with one another. These are preferably organometallic compounds such as tin(II) salts of organic carboxylic acids, e.g. tin(II) dioctoate, tin(II) dilaurate, dibutyltin diacetate and dibutyltin dilaurate, and tertiary amines such as tetramethylethylenediamine, N-methylmorpholine, diethylbenzylamine, triethylamine, dimethylcyclohexylamine, diazabicyclooctane, N,N′-dimethylpiperazine, N-methyl-N′-(4-N-dimethylamino)butylpiperazine, N,N,N′,N″,N″-pentamethyldiethylenetriamine or the like. Further useful catalysts include: amidines, for example 2,3-dimethyl-3,4,5,6-tetrahydropyrimidine, tris(dialkylaminoalkyl)-s-hexahydrotriazines, especially tris(N,N-dimethylaminopropyl)-s-hexahydrotriazine, tetraalkylammonium hydroxides, for example tetramethylammonium hydroxide, alkali metal hydroxides, for example sodium hydroxide, and alkali metal alkoxides, for example sodium methoxide and potassium isopropoxide, and alkali metal salts of long chain fatty acids having 10 to 20 carbon atoms and optionally pendant OH groups. According to the reactivity to be established, the catalysts are employed in amounts of 0.001% to 0.5% by weight, based on the isocyanate component.
The elastomers of the invention, especially polyurethanes or shaped bodies, differ from the products based on monomeric, room temperature solid diisocyanates known from the prior art, preferably those based on naphthalene 1,5-diisocyanate, in that, by virtue of the method of the invention, the contamination of the monomeric, room temperature solid diisocyanate recovered from the residue with these auxiliaries can also be minimized.
Such cellular PUR cast elastomers, also referred to as shaped bodies, find use as damping elements in vehicle construction, for example in automobile construction, for example as overload springs, buffers, transverse link bearings, rear axle subframe bearings, stabilizer bearings, longitudinal strut bearings, suspension strut bearings, shock absorber bearings, or bearings for wishbones, and also as an emergency wheel on the rim, which has the effect that the vehicle, for example in the event of tire damage, runs on the cellular elastomer and remains controllable. The bulk cast elastomers can also be used as a coating for rolls, wheels and drums, squeegees, screens or hydrocyclones.
The present invention is more particularly elucidated hereinafter with reference to examples and comparative examples, but without restricting it thereto.
Monomeric naphthalene diisocyanate (NDI) was separated from distillation residues by various methods. For this purpose, the distillation residue was mixed with various polyisocyanates and subjected to a distillation.
The following polyisocyanates were used:
Polyisocyanate 1: an aliphatic polyisocyanate based on pentamethylene diisocyanate (PDI) and having an NCO content of 21.9% by weight and a viscosity of 9500 mPas at 23° C.
Polyisocyanate 2: an aliphatic polyisocyanate based on hexamethylene diisocyanate (HDI) and having an NCO content of 11.0% by weight and a viscosity of 6000 mPas at 23° C.
Polyisocyanate 3: an aliphatic polyisocyanate based on hexamethylene diisocyanate (HDI) and having an NCO content of 21.8% by weight and a viscosity of 3000 mPas at 23° C.
Polyisocyanate 4: an aliphatic polyisocyanate based on hexamethylene diisocyanate (HDI) and having an NCO content of 23.0% by weight and a viscosity of 1200 mPas at 23° C.
Polyisocyanate 5: an aromatic polyisocyanate based on diphenylmethane diisocyanate (MDI) and having an NCO content of 31.3% by weight and a viscosity of 680 mPas at 25° C.
All viscosity measurements were recorded with a Physica MCR 51 rheometer from Anton Paar Germany GmbH (DE) in accordance with DIN EN ISO 3219:1994-10 at a shear rate of 250 s-1.
The residual monomer contents were adjusted by addition of the appropriate monomeric diisocyanate (PDI, HDI or MDI) for the examples in table 1 and measured according to DIN EN ISO 10283:2007-11 by gas chromatography with an internal standard.
The purity of the NDI was determined by gas chromatography. The measurements were effected using a Hewlett Packard HP 6890 with an FID detector and HP-Chemstation software using an Optima 5 column and the following parameters: split rate: 8.31:1 mL/min; flow rate: 96.4 mL/min; pressure: 0.7 bar, carrier gas: helium, injection volume: 1 μL, inliner straight split liner filled with Carbofritt.
The NDI residues before and after distillation were analyzed by means of GPC to DIN 55672-1:2007-08. The yield was then determined by subtracting the area percentage of the monomer still remaining from the area percentage of the original amount of monomer, which were determined in each case by GPC to DIN 55672-1:2007-08.
The figures in % by weight for the mixture are based on the mass the overall mixture. The residual monomer content is based on the mass of the respective polyisocyanate used. The respective mixture was sent to a vacuum distillation in a thin-film evaporator under the conditions specified, with condensation of the monomeric 1,5-NDI in solid form. The bottoms output that was still liquid at this temperature consisted in each case of 1,5-NDI monomer, non-distillable components and poly isocyanate. All examples and comparative examples were conducted inacomentional glass thin-film evaporator with an exaporator area of 0.1 m2 (diameter 100 mm, length 300 mm).
Comparison of inventive examples 1 to 7 with comparative examples 9 to 11 shows that the method of the invention can recover high proportions of the room temperature solid diisocyanate from the distillation residue, and demonstrates the significance of the residual monomer content in the additive polyisocyanate since, in the case of relatively high residual monomer contents in the comparative examples, there was conglutination in the thin-film evaporator and it was not possible to condense the monomeric 1,5-NDI in solid form. The proportion of recovered monomeric 1,5-NDI monomer is not determinable analytically here. Comparative example 9 shows that, without addition of the polyisocyanate of the invention, distillation was possible only at a distinctly reduced dosage rate and led to a distinctly lower yield.
A further advantage of the method of the invention is that the bottoms output is free-flowing since further oligomerization reactions have been very substantially suppressed by the low temperatures and shorter thermal stress in the performance of the method of the invention compared to conventional methods, which constitutes a significant advantage for the continuous mode of operation. The room temperature solid diisocyanates obtained from the method of the invention are notable for high purity and can be used without restrictions for production of elastomers.
| Number | Date | Country | Kind |
|---|---|---|---|
| 20153028.4 | Jan 2020 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2021/051094 | 1/20/2021 | WO |
