Classifications

• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/08—Processes
  • C08G18/16—Catalysts
  • C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
  • C08G18/20—Heterocyclic amines; Salts thereof
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/02—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only
  • C08G18/027—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only the polymeric products containing urethodione groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/02—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only
  • C08G18/022—Polymeric products of isocyanates or isothiocyanates of isocyanates or isothiocyanates only the polymeric products containing isocyanurate groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/08—Processes
  • C08G18/16—Catalysts
  • C08G18/18—Catalysts containing secondary or tertiary amines or salts thereof
  • C08G18/20—Heterocyclic amines; Salts thereof
  • C08G18/2009—Heterocyclic amines; Salts thereof containing one heterocyclic ring
  • C08G18/2036—Heterocyclic amines; Salts thereof containing one heterocyclic ring having at least three nitrogen atoms in the ring
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
  • C08G18/72—Polyisocyanates or polyisothiocyanates
  • C08G18/80—Masked polyisocyanates
  • C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
  • C08G18/807—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with nitrogen containing compounds

Definitions

• the invention relates to a new process for the preparation of polyisocyanates, the polyisocyanates thus produced and their use.
• the oligomerization of isocyanates is a long-known, well-established method for modifying generally difunctional, low molecular weight isocyanates to give products with advantageous application properties, e.g. in the paint and coating agent sector, generally called polyisocyanates in the present document (J Prakt. Chem./Chem. Ztg. 1994, 336, 185-200.).
• Polyisocyanates based on aliphatic diisocyanates are generally used for lightfast, non-yellowing lacquers and coatings.
• aliphatic refers to the carbon atoms to which the NCO groups of the monomer are attached, i.e. in the molecular structure can be aromatic
• Rings are included, which then by definition do not carry any NCO groups.
• trimers or trimerizates are generally referred to, otherwise the exact name chosen. Dimerization and uretdione formation are used interchangeably.
• oligomerization encompasses all types of modification.
• the aim is to achieve a high conversion in the reaction accompanied by a high resin yield in the subsequent workup step with a good level of properties of the polyisocyanate resins.
• Dimers based on aliphatic diisocyanates have a significantly lower viscosity than trimers. Regardless of the degree of conversion or the resin yield, however, they are strictly linear, ie NCO difunctional. Trimers, on the other hand, have the higher functionality required for a high crosslinking density in the polymer and, as a result, good resistance properties of the same. Your
• trimer-type polyisocyanates isocyanate oligomerization using a large number of catalysts which are both salt-like and covalently structured (J Prakt. Chem./Chem. Ztg. 1994, 336, 192-196 and the literature cited therein). While using salt-like compounds such as e.g. Carboxylates (e.g. DE-A 3 100 263), fluorides (e.g. EP-A 339 396) or hydroxides (e.g.
• salt-like compounds such as e.g. Carboxylates (e.g. DE-A 3 100 263), fluorides (e.g. EP-A 339 396) or hydroxides (e.g.
• EP-A 330 966 for isocyanate oligomerization require very small amounts of catalyst and achieve the desired conversion in a very short time, when using covalently structured trimerization catalysts, higher catalyst concentrations and / or longer reaction times are required.
• An example of this is the oligomerization of aliphatic diisocyanates with N-silyl compounds, described e.g. in EP-A 57 653, EP-A 89 297, EP-A 187 105, EP-A 197 864 and WO 99/07765.
• the object described above has been achieved as a catalyst for isocyanate oligomerization by using salt-like derivatives of five-membered N-heterocycles which carry at least one hydrogen atom bonded to a ring nitrogen atom in the neutral molecule.
• the invention is based on the surprising observation that salt-like derivatives of five-membered N-heterocycles which carry at least one hydrogen atom bonded to a ring nitrogen atom in the neutral molecule catalyze isocyanate oligomerization and that, in addition to isocyanate trimers, uretdione structures are also formed to a considerable extent.
• Nitrogen heterocycles have already been introduced as neutral compounds bearing NH or N-alkyl groups in polyisocyanate chemistry. However, they are mostly used as blocking agents for NCO groups (derivatives containing NH groups, cf. EP-A 0 741 157) or as a stabilizer against damage to the Polyisocyanates produced paint film used by UV rays.
• Substituted benzotriazoles which contain further OH groups in the molecule, cf. eg DE-A 198 28 935, WO 99/67226 and cited therein. Literature.
• WO 99/23128 describes a system, etc. consisting of a "trimerization catalyst” and imidazole.
• the invention relates to a process for the catalytic oligomerization of isocyanates, characterized in that the oligomerization catalysts used are salt-like compounds which contain five-membered N-heterocycles as an anion, the neutral form of the heterocyclic anion being based on N-heterocylene which contains at least one NH- Have function as part of the five-membered ring system.
• the invention further relates to the polyisocyanates obtained by this process and their use for the production of polyurethane plastics and coatings.
• the catalysts according to the invention are tested in a miniaturized and parallel mode of operation. This enables a large number of catalysts to be checked simultaneously for activity and product selectivity.
• the neutral compounds on which the heterocyclic anion is based are species of the general formula (4)
• R can represent identical or different radicals from the following series: H, Cj-
• pyrrole, substituted pyrroles and carbocyclic and / or heterocyclic fused derivatives of pyrrole can be used as the neutral compounds on which the heterocyclic anion is based.
• the neutral compounds on which the heterocyclic anion is based can be pyrazole and / or imidazole, substituted pyrazoles and or imidazoles and carbocyclically and / or heterocyclically fused derivatives of pyrazole and / or imidazole.
• tetrazoles and substituted tetrazoles are used as the neutral compounds on which the heterocyclic anion is based.
• the at least one hydrogen atom bound to a ring nitrogen atom wear examples include pyrrole, indole, carbazole and substituted derivatives such as 5-nitroindole or 5-methoxyindole, pyrazole, indazole and substituted derivatives such as 5-nitroindazole, imidazole and substituted derivatives such as 4-nitroimidazole or 4-methoxyimidazole, benzimidazole or substituted benzimidazoles, for example 5- nitrobenzimidazole, 5-methoxybenzimidazole, 2-trifluoromethylbenzimidazole, heteroaromatic fused imidazoles such as pyridinoimidazole or purine, 1,2,3-triazole and substituted derivatives such as 4-chloro-5-carbomethoxy-l, 2,3-triazole or 4-chloro -5- cyano-l, 2,3-triazole, 1,2,4-triazole and substituted derivatives such as 3,5-dibro
• the salts of the above-mentioned nitrogen heterocycles are also commercially available, for example in the form of their sodium salts.
• their preparation for example if counterions other than Na + to the catalytically active anion are to be used, is very simple using methods known from the literature. Further details can be found in the examples.
• the optimal “design” of the anion with regard to the catalytic activity, the thermal stability and the selectivity of the reaction with respect to the isocyanate oligomer types formed can be adapted to the isocyanate to be oligomerized by suitable substituents on the five-membered heterocyclic ring.
• the OHgomerization catalysts used are those which, as the cation, contain alkali metal, alkaline earth metal and / or monovalent ammonium and / or phosphonium cations of the general formula (5)
• E represents nitrogen (N) or phosphorus (P) and R 1 , R 2 , R 3 and R 4 independently of one another represent identical or different radicals, and in each case a saturated aliphatic or cycloaliphatic, an optionally substituted aromatic or araliphatic radical with bis to 18 carbon atoms.
• Catalysts are largely uncritical. If it is desired to separate the catalyst or its secondary products formed in the course of the deactivation from the product following the oligomerization reaction, it can be advantageous to use polar, highly charged counterions such as, for example, alkali metal or alkaline earth metal ions. If a homogeneous distribution of the catalyst in the isocyanate (mixture) used for the reaction and in the polyisocyanate resin is desired, lipophilic representatives such as ammonium or phosphonium species are selected.
• the latter can be easily prepared, for example, by simply combining a sodium triazolate and an onium chloride, preferably in solvents which do not dissolve the sodium chloride which precipitates well, and bring them to the desired concentration and purity by filtration and subsequent concentration. In the latter work-up step, residues of sodium chloride initially still dissolved generally also precipitate out and can be filtered off.
• onium chlorides examples include tetra-methyl-, -ethyl-, -propyl-, -butyl-, -hexyl- and octyl-ammonium chloride, but also mixed substituted ammonium salts such as benzyl-trimethylammonium chloride or methyl-trialkylammonium- chloride where alkyl represents straight-chain or branched C 8 to C 10 residues (trade name e.g.
• Aliquat ® or Adogen ® as well as tetra- ethyl, propyl, butyl, hexyl and octyl phosphonium chloride, but also mixed substituted phosphonium salts such as alkyl triethyl, tributyl, trihexyl, trioctyl and / or tridodecyl phosphonium chloride, where alkyl for straight-chain or branched C to C 20 radicals (trade name eg Cyphos ® such as Cyphos ® 443, Cyphos ® 3453, Cyphos ® 3653 etc.).
• Cyphos ® such as Cyphos ® 443, Cyphos ® 3453, Cyphos ® 3653 etc.
• catalyst concentrations based on the mass of (poly) isocyanate (mixture) used and the mass of the catalyst used, are sufficient between 5 ppm and 5%, preferably between 10 ppm and 2%.
• the catalysts used in the process according to the invention can be used in bulk or in solution.
• all substances in which the catalyst is soluble without decomposition and which do not or only react with isocyanates to give non-disruptive secondary products common in polyurethane chemistry, such as ureas, biurets, urethanes and allophanates, are suitable as solvents.
• catalyst solvents preference is given to using compounds which react with the diisocyanates used as the starting component to give secondary products common in polyurethane chemistry and therefore do not have to be separated off after the reaction. These include straight-chain or branched, possibly more than one OH
• Group-containing alcohols with 1 to 20 carbon atoms which optionally contain further heteroatoms, preferably oxygen, in the molecular structure.
• Examples include its methanol, ethanol, 1- and 2-propanol, the isomeric butanols, 2-ethylhexanol, 2-ethylhexan-l, 3-diol, 1,3- and 1,4-butanediol and l-methoxy-2-propanol , It is particularly advantageous that the above-mentioned catalysts can also be used in a very concentrated solution, and yet hardly at all Formation of spontaneous cross-linkages in the oligomerizing isocyanate.
• the method according to the invention can be operated in a continuous manner, e.g. in a tubular reactor.
• all aliphatic isocyanates pure or as a mixture with one another, are suitable as isocyanates to be oligomerized in the process according to the invention.
• NCO groups In addition to the NCO groups, they have 4 to 20 carbon atoms in the carbon backbone. They can contain aliphatic and / or cycloaliphatic bound NCO groups.
• All regio- and stereoisomers of the isocyanates mentioned below are mentioned by way of example: bis (isocyanatoalkyl) ether, bis- and tris (isocyanato-alkyl) -benzenes, -toluenes, and -xylenes, propane diisocyanates, butane diisocyanates, pentane diisocyanates, hexane diisocyanates (eg hexamethylene diisocyanate, HDI), heptane diisocyanates, octane diisocyanates, nonandi- (e.g.
• trimethyl-HDI, TMDI usually as a mixture of the 2,4,4- and 2,2,4-isomers
• tri-isocyanates e.g. 4-iso- cyanatomethyl-l, 8-octane diisocyanate
• decane and triisocyanates undecane and triisocyanates
• dodecanedi and triisocyanates 1,3- and 1,4-bis- (isocyanatomethyl) cyclohexanes (H 6 XDI), 3-isocyanatomethyl-3,5,5-trimethylcyclohexyl isocyanate (isophorone diisocyanate, IPDI), bis- (4-isocyanatocyclohexyl) methane (H 12 MDI) and bis (isocyanatomethyl) norbornane (NBDI).
• HDI, TMDI, methylpentane-1,5-diisocyanate (MPDI) H 6 XDI, NBDI
• HDI hexamethylene diisocyanate
• TMDI trimethyl-HDI
• MPDI 2-methylpentane-l
• IPDI isophorone diisocyanate
• 1,3- and 1,4- are preferably used as isocyanates to be oligomerized.
• the production process for the starting isocyanates to be used in the process according to the invention is not critical for carrying out the process according to the invention, so the starting isocyanates may have been generated with or without the use of phosgene.
• the catalytic conversion according to the invention can in principle be carried out at any technically feasible temperature. Reaction temperatures above 0 ° C. are preferred, preferably between 20 and 100 ° C., particularly preferably between 40 and 100 ° C.
• the polyisocyanates according to the invention can be isolated and purified by the customary methods of the prior art, such as thin-film distillation, extraction, crystallization and / or molecular distillation. They occur as colorless or only weakly colored liquids or solids.
• the polyisocyanates produced according to the invention are versatile starting materials for the production of polymers such as optionally foamed plastics, polyurethane lacquers, coating agents, adhesives and additives.
• the polyisocyanates according to the invention are generally mixed with OH and / or NH
• any other binder components and paint solvents or paint solvent mixtures used such as toluene, xylene, cyclohexane, chlorobenzene, butyl acetate, ethyl acetate, ethyl glycol acetate, methoxypropylacetate, acetone, white spirit, higher substituted aromatics (Solventnaphtha®, Solellsol®), Solvesso® Isopar®, Nappar®, Diasol®), other auxiliaries and additives can also be used in the coatings, such as, for example, wetting agents, leveling agents, anti-skinning agents, anti-foaming agents, matting agents, viscosity regulators, pigments, dyes, UV absorbers, catalysts and stabilizers against thermal and oxidative influences.
• wetting agents wetting agents, leveling agents, anti-skinning agents, anti-foaming agents, matting agents, viscosity regulators, pigments, dyes, UV absorbers, catalysts
• the polyisocyanates based on the oligomer mixtures produced according to the invention can be used for coating or as an additive for finishing a large number of materials, such as, for example, wood, plastic, leather, metal, paper, concrete, masonry, ceramic and textile.
• the NCO content of the resins described in the examples and comparative examples is determined by titration according to DTN 53 185.
• the dynamic viscosities of the polyisocyanate resins are determined at 23 ° C. using the VT 550 viscometer, PK 100 plate-cone measuring arrangement, from Haake. Measurements at different shear rates ensure that the flow behavior of the described polyisocyanate mixtures as well as that of the comparison products corresponds to the ideal Newtonian liquids. The specification of the shear rate can therefore be omitted.
• the indication of mol% or the molar ratio of different structure types to one another is based on NMR spectroscopic measurements. Unless stated otherwise, it always relates to the sum of the structure types formed by the modification reaction (oligomerization) from the previously free NCO groups.
• the measurements are carried out on the DPX 400 from Bruker on approx. 5% (1H-NMR) or approx. 50% ( 13 C-NMR) samples in dry CDC1 3 at a frequency of 400 MHz ( 1H-NMR) or 100 MHz ( 13 C-NMR).
• As a reference for the ppm scale small amounts of tetramethylsilane in the solvent with a ⁇ -chem. Shift of 0 ppm ( !
• Sodium 1,2,4-triazolate and Na imidazolate are commercially available from Aldrich or can be prepared by deprotonating 1,2,4-triazole or imidazole, for example with a methanolic solution of sodium methoxide, Na MeO "
• the methanolic solutions of the sodium salt obtained in this way have been used as such for the catalysis, if appropriate after recrystallization of the salt, and are moreover used for the preparation of catalyst systems other than the Na cation as counterions to the azolate anion the NH-acidic neutral compounds with other alkali or alkaline earth alcoholates or hydroxides (Li, K, NE, Mg etc.) can be used to generate further catalyst systems, both in the invention
• Alkali or alkaline earth cations can be used as counterions to the azolate anion.
• Tetrabutylphosphonium derivative described.
• Other Na derivatives, other alkali or alkaline earth derivatives (see Table 1) and other tetraalkylammonium and phosphonium derivatives (see Table 2) are obtained completely analogously.
• Triazole A 1 M solution of this Na-1,2,3-triazolate in DMSO is prepared for catalysis experiments.
• Na azolate compounds are obtained in a completely analogous manner from the underlying NH compounds (Table 1).
• the compounds are dissolved in the solvents listed in Table 1.
• Ammonium chlorides are obtained from Aldrich, phosphonium chlorides, possibly in dissolved form, from Cytec.
• the active catalyst content is determined after working up by simple acidimetric titration with 0.1N HCl.
• the solutions thus obtained can be used undiluted or diluted, depending on the field of application. Table 2 shows the dilution used
• a Rolhand vessel with a septum closure is evacuated twice and filled with argon. 5 ml of dusocyanate are poured into the vessel prepared in this way with the aid of a syringe, and the corresponding amounts of catalyst solution are then added with stirring.
• the catalyst numbers cf. Tables 1 and 2 each refer to the amount of object Dusocyanate and catalyst used to achieve the conversion achieved in the respective experiments.
• the reaction mixture obtained is reacted in an oil bath or in a stirred heating block (for example Variomag reaction block type 48.2 / RM from H&P) at the desired temperature.
• the crude product thus obtained is then freed from the unreacted monomer by thin-layer distillation at 120 ° C./0.1 mbar in a short-path evaporator.
• the distillation residue obtained is 572.9 g, corresponding to 34.1% resin yield, of an almost colorless polyisocyanate resin with the following data: NCO content: 23.0%, viscosity at 23 ° C: 280 mPas, free monomer: 0.11% ,
• NCO content 23.0%
• viscosity at 23 ° C: 280 mPas free monomer: 0.11%
• Polyisocyanate resin is determined as described in the introduction: 51 mol% uretdiones, 22.4 mol% isocyanurates, 26.6 mol% iminooxadiazinediones.
• the recovered HDI can be used again without any problems.

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• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Organic Chemistry (AREA)
• Polyurethanes Or Polyureas (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
• Catalysts (AREA)
• Paints Or Removers (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

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