EP3697828A1 - Oligocarbonatpolyole aus dianhydrohexitol-dialkylcarbonat oder einem dimer von dianhydrohexitol-dialkylcarbonat, verfahren zu ihrer herstellung und ihre verwendung - Google Patents

Oligocarbonatpolyole aus dianhydrohexitol-dialkylcarbonat oder einem dimer von dianhydrohexitol-dialkylcarbonat, verfahren zu ihrer herstellung und ihre verwendung

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Publication number
EP3697828A1
EP3697828A1 EP18796733.6A EP18796733A EP3697828A1 EP 3697828 A1 EP3697828 A1 EP 3697828A1 EP 18796733 A EP18796733 A EP 18796733A EP 3697828 A1 EP3697828 A1 EP 3697828A1
Authority
EP
European Patent Office
Prior art keywords
monomer
diol
carbonate
dianhydrohexitol
dimer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP18796733.6A
Other languages
English (en)
French (fr)
Inventor
Jean-Marc Corpart
René SAINT-LOUP
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Roquette Freres SA
Original Assignee
Roquette Freres SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Roquette Freres SA filed Critical Roquette Freres SA
Publication of EP3697828A1 publication Critical patent/EP3697828A1/de
Pending legal-status Critical Current

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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
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/20—General preparatory processes
    • C08G64/30—General preparatory processes using carbonates
    • C08G64/305—General preparatory processes using carbonates and alcohols
    • 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
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/42—Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/44—Polycarbonates
    • 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
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/02—Aliphatic polycarbonates
    • 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
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/02—Aliphatic polycarbonates
    • C08G64/0208—Aliphatic polycarbonates saturated
    • 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
    • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
    • C08G64/40—Post-polymerisation treatment
    • C08G64/403—Recovery of the polymer

Definitions

  • the present invention relates to novel oligocarbonate polyols, obtained by reaction between a dialkylcarbonate of dianhydrohexitol and / or a dimer of dianhydrohexitol carbonate and another diol and / or triol, under particular reaction conditions and in particular relative amounts of the species used. Thu.
  • ether components polytetramethylene glycol
  • esters from adipate in particular
  • polylactone polycaprolactone base among others
  • polycarbonate diols are one of the starting raw materials of these polyurethane resins.
  • the ethers have good resistance to hydrolysis, they are less so with respect to light and heat.
  • the esters exhibit diametrically opposite behavior with respect to these same properties.
  • polycaprolactones they are also deficient with regard to hydrolysis phenomena. It is therefore recognized that polycarbonates diols present to date the best compromise in order to obtain a durable quality for the final product, in terms of resistance to hydrolysis, heat and light. This is particularly important for a polyurethane coating, especially in applications such as exterior paints which are precisely exposed to the aforementioned constraints.
  • oligocarbonates diols their synthesis is also well-known in the prior art. These products are prepared from aliphatic polyols which react with phosgene, bischlorocarbon esters, diaryl carbonates, these cyclic carbonates or dialkyl carbonates. In this regard, reference may be made to document US 2005 065360.
  • the person skilled in the art must now incorporate new constraints. particularly of an environmental nature. The development of polymeric materials derived from renewable resources in the short term has indeed become a major ecological and economic imperative, faced with the depletion and rising prices of fossil resources such as oil.
  • the second describes a polycarbonate diol consisting of a diol and a dianhydrohexitol selected from isosorbide, isomannide and isoidide, and having a weight average molecular weight of between 250 and 5,000 as determined by NMR, while by having a ratio in number of alkyloxy or aryloxy terminal groups relative to the total number of end groups greater than or equal to 5%.
  • EP 2 559 718 which describes the simultaneous reaction between a diol selected from isosorbide, isomannide and isoidide, another diol, and a diester carbonate, such as diphenyl carbonate.
  • a polycarbonate diol is obtained here, but with a completely statistical architecture because the diester carbonate is very reactive, it reacts without preference with both the dianhydrohexitol and the other diol.
  • the final properties of the product such as its resistance to hydrolysis, light and heat being directly related to its architecture, said polycarbonate diol will have fluctuating properties depending on its final architecture. This lack of control of the level of properties can not accommodate an industrial use for the product in question.
  • oligocarbonates polyols advantageously implementing a naturally occurring monomer such as a dianhydrohexitol and without using phosgene and without generating phenol during the reaction, and finally while allowing itself to regulate From the architecture of the synthesized product, the applicant company has been able to develop the following process, consisting in reacting a dialkyl carbonate of dianhydrohexitol and / or a dimer of dianhydrohexitol carbonate with another diol and / or triol, to obtain oligocarbonates polyols. presenting an alternating architecture perfectly controllable and controlled.
  • diol polycarbonates which can be used in the manufacture of adhesives, are obtained from various coatings such as paints, lacquers and varnishes. These oligocarbonates polyols may in particular be used to produce polyurethane resins, with particularly advantageous properties, in terms of resistance to abrasion, scratching and UV.
  • the dialkycarbonates of isosorbide which come into play in the reaction are manufactured according to the method described in the patent application WO 201 1/039483.
  • This comprises reacting at least one dianhydrohexitol, at least 2 molar equivalents of a di (alkyl) carbonate and a transesterification catalyst.
  • this method does not generate compounds harmful to humans or dangerous for the environment.
  • EP 2 033 981 described a synthesis whose disadvantage was the formation of phenol, which then had to be distilled and removed as a reaction by-product.
  • documents US 2004/241553 and JP 06-261774 they relied on the use of toxic chloroformic esters.
  • the present invention relates to a process for manufacturing an oligocarbonate polyol devoid of aromatic groups and phenolic functions comprising:
  • a step (1) of introduction into a reactor :
  • R 3 and R 4 are the same or different alkyl groups, or a mixture of (A1) and (A2); ⁇ a step (2) introducing into the reactor a monomer diol (B1) or a triol monomer (B2) or a mixture of (B1) and (B2), (B1) and ( B2) being both different from (A1) and (A2); the molar ratio in the reactor of (A1) and (A2) with respect to (B1) and (B2) corresponding to the following formula:
  • the invention relates to an oligocarbonate polyol obtainable by the method of the invention.
  • the invention relates to a process for the preparation of a polymeric material, in particular intended for the preparation of an adhesive, a paint, a lacquer, a varnish or a resin, such as a polyurethane resin, characterized in that the oligocarbonate polyol according to the invention is reacted with a monomer having at least two functions each capable of reacting with a hydroxyl function.
  • oligocarbonate polyol any polymer comprising repeating units, formed by the reaction of monomers or dimers, linked by carbonate bonds and in particular the repeating units described above and whose chain terminations are hydroxyl functions. These repeating units are formed by reaction of the monomer (A1) and / or the dimer (A2) with the monomers (B1) and / or (B2) already presented above.
  • the expression “a monomer” extends to mixtures of this monomer.
  • the expression “a monomer (A1)” or “a monomer of formula (A1)” means that only one monomer of formula (A1) is used or that a mixture of different monomers of formula (A1) is used.
  • a similar meaning is given to the terms “a monomer (A2)” or “a dimer of formula (A2)", “a monomer (B1)” or “a monomer of formula (B1)", or “a monomer (B2 ) "Or” a monomer of formula (B2) ".
  • the invention relates to a process for producing hydroxytelechelic oligocarbonates by polycondensation of the monomer (A1) and / or dimer (A2) and monomers (B1) and / or (B2).
  • 1,4-3,6-dianhydrohexitol or "dianhydrohexitol” as used in the present invention includes isosorbide (obtained by dehydration of D-glucitol), isomannide (obtained by dehydration of D-mannitol). and isoidide (obtained by dehydration of D-iditol).
  • dianhydrohexitol carbonate dimer according to the present invention is meant a compound of formula (A2), that is to say consisting of two molecules of dianhydrohexitol monoalkylcarbonate interconnected by a bivalent carbonate function. The compound thus comprises in total two carbonate termini.
  • the monomer (A1) used in step (1) may be chosen from isosorbide dialkylcarbonate, isomannide dialkylcarbonate and isoidide dialkylcarbonate.
  • the monomer (A1) may contain one or more dianhydrohexitol dialkylcarbonates but preferably contains a single dianhydrohexitol dialkylcarbonate, in particular an isosorbide dialkylcarbonate, available in greater quantity and at a lower cost than the other two stereoisomers.
  • the alkyl groups R 1 and R 2 borne by the monomer (A 1) can comprise from 1 to 10 carbon atoms, in particular from 1 to 6 carbon atoms, for example from 1 to 4 carbon atoms, and are particularly chosen from methyl or ethyl groups.
  • the monomer (A1) is an isosorbide dialkylcarbonate, in particular an isosorbide diethyl carbonate or an isosorbide dimethyl carbonate.
  • the monomer (A1) can be obtained using, for example, already known processes for the manufacture of dianhydrohexitol dialkylcarbonate.
  • the monomer (A1) is prepared according to the process described in the patent application WO 201 1/039483 (in the name of Roquette Fromme) by reacting a dianhydrohexitol with at least 2 molar equivalents of a di (alkyl) carbonate. ) and a transesterification catalyst.
  • the formation of dimers can be inhibited by the use of a large excess of dialkyl carbonate. This method has the advantage of not generating compounds harmful to humans or dangerous for the environment.
  • the dimer (A2) used in step (1) is a dimer of (A1). Depending on the dianhydrohexitol used, one or more conformations of dimers (A2) can be obtained.
  • the dimer (A2) may be selected from an isosorbide carbonate dimer, an isomannide carbonate dimer, or an isoidide carbonate dimer.
  • the dimer (A2) may contain one or more dimers of dianhydrohexitol carbonate but preferably contains a single dianhydrohexitol carbonate dimer, in particular an isosorbide carbonate dimer, available in greater quantity and at a lower cost than both. other stereoisomers.
  • the alkyl groups R 3 and R 4 carried by the dimer (A2) can comprise from 1 to 10 carbon atoms, in particular from 1 to 6 carbon atoms, for example from 1 to 4 carbon atoms, more particularly are chosen from methyl or ethyl groups.
  • the dimer (A2) is an isosorbide carbonate dimer, in particular an isosorbide ethylcarbonate dimer or an isosorbide methylcarbonate dimer.
  • the dimer (A2) can be produced by reacting, for example in a first step, one mole of dianhydrohexitol with one mole of alkyl chloroformate in order to form dianhydrohexitol monoalkylcarbonate, then in a second step one mole of phosgene with two moles of dianhydrohexitol monoalkylcarbonate formed in the first step.
  • Another possibility of manufacturing the monomer (A1) and the dimer (A2) is to use a process allowing their simultaneous synthesis. Indeed, the Claimant has also to the point a method for making such a mixture. This process is described in detail in International Application No. WO201 1/039483.
  • This preparation method comprises, in the order, the following steps:
  • a transesterification catalyst such as, for example, potassium carbonate
  • the solution obtained at the end of the process comprises a mixture of monomer (A1) and dimer (A2) with dialkyl carbonate. Distillation is carried out and the mixture of (A1) and (A2) free of dialkyl carbonate is recovered.
  • the ratio (A1) / (A2) can be varied by modifying the initial reaction mixture: it advantageously contains from 2.1 to 100 molar equivalents, preferably from 5 to 60 molar equivalents, and in particular from 10 to 40 molar equivalents. molar equivalents of dialkyl carbonate, based on the amount of dianhydrohexitol initially present in the reaction medium. The higher the amount of dialkyl carbonate, the higher the ratio (A1) / (A2).
  • the Applicant has found that by reacting isosorbide and dimethyl carbonate in the presence of potassium carbonate under the conditions of the method described above, a solution comprising (A1) and (A2) could be obtained. with a ratio (A1) / (A2) ranging from about 4 (when the ratio of dialkyl carbonate / isosorbide is 10) to about 20 (when the ratio of dialkyl carbonate / isosorbide is 40).
  • This method of simultaneous synthesis of (A1) and (A2) has the advantages of using less toxic reagents than the alkyl chloroformate used in the process described in JP 06-261774 for example; co-products of synthesis are also less toxic that the chlorinated species emitted during the synthesis with chloroformate (methanol in the case where the alkyl is a methyl, ethanol in the case where the alkyl is an ethyl).
  • step (1) only the monomer (A1) is synthesized. Only this is introduced into the reactor in step (1), that is to say that dimer (A2) is not introduced into the reactor.
  • a mixture of monomer (A1) and dimer (A2) is synthesized. This mixture is introduced into the reactor in step (1).
  • Monomers (B1) and (B2) are monomers (B1) and (B2)
  • the diol monomer (B1) and the triol monomer (B2) may be chosen from aliphatic diols or triols, in particular linear or branched, or cyclic diols or triols, aromatic or nonaromatic. In one embodiment, the diol (B1) or triol (B2) comprises from 2 to 14 carbons.
  • the linear aliphatic diol (without branching) can be chosen from the following diols: ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-pentanediol, 1,6-hexanediol, 1,8-octanediol, 1 10-decanediol, preferably ethylene glycol, 1,4-butanediol or 1,6-hexanediol.
  • the linear aliphatic triol may be chosen from the following triols: glycerol, 1,2,4-trihydroxybutane, 1, 2,5-trihydroxypentane or 1,2,6-trihydroxyhexane.
  • the branched aliphatic diol (with unreactive pendent chains) may be chosen from the following diols: 1,2-propanediol, 1,3-butanediol, 2,3-butanediol, 1,3-pentanediol, 1,4 hexanediol, 2,2-dimethyl-1,3-propanediol, 3-methyl-1,5-pentanediol, 2,2-dimethyl-1,3-propanediol or 2-methyl-1,3-propanediol.
  • the cyclic diol or triol may comprise one or more rings, for example from 2 to 4 rings, preferably 2 rings. Each cycle preferably comprises from 4 to 10 atoms.
  • the atoms included in the rings can be chosen from carbon, oxygen, nitrogen or sulfur.
  • the constituent atoms of the ring are carbon or carbon and oxygen.
  • the aromatic diol preferably comprises from 6 to 24 carbon atoms.
  • the non-aromatic cyclic diol may comprise from 4 to 24 carbon atoms, preferably from 6 to 20 carbon atoms.
  • the cyclic aliphatic diol may be chosen in particular from the following diols:
  • ⁇ dianhydrohexitols such as isosorbide, isomannide and isoidide, which are heterocyclic diols biosourcés;
  • cyclohexanedimethanols such as 1, 2-cyclohexanedimethanol, 1, 3- cyclohexanedimethanol, and 1, 4-cyclohexanedimethanol;
  • Cyclohexanediols such as 1, 2-cyclohexanediol, 1,3-cyclohexanediol and 1,4-cyclohexanediol;
  • aromatic cyclic diol may be chosen in particular from the following diols:
  • the aromatic cyclic triol may be chosen from the following triols: pyrogallol, hydroxyquinol, phloroglucinol.
  • Monomers other than (A1), (A2), (B1) and (B2) can be introduced according to the process of the invention.
  • monomers comprising more than 2 alcohol or alkyl carbonate functions may be introduced. It is also possible to introduce monomers comprising several functional groups chosen from the carboxylic acid, carboxylic acid ester or amine function or mixtures of these functions. It is also possible to introduce other monomers such as dianhydrohexitol monoalkylcarbonate, oligomers of (A1) with a degree of polymerization greater than or equal to 3.
  • the monomers introduced into the reactor consist essentially of (A1), (A2), (B1) and (B2).
  • the amount of diaryl carbonate and halogenated monomers introduced for example to amounts less than 5% of the total number of moles of monomers introduced.
  • no monomer selected from diaryl carbonates and halogenated monomers is introduced.
  • the molar ratio in the reactor of (AD and (A2) with respect to (B1) and (B2) as defined above is strictly less than 1 and greater than 0.5, in particular strictly less than 1 and greater than 0.7, more particularly strictly less than 1 and greater than 0.9.
  • Step (1) can be carried out before step (2) or vice versa. These two steps can also be performed simultaneously.
  • a premix of (A1) and / or (A2) and (B1) and / or (B2) is carried out before introducing them into the reactor.
  • dimer (A2) When dimer (A2) is used in the process, it can be introduced in admixture with (A1). This mixture can be for example made directly according to the synthesis method described in International Application No. WO 2012/136942.
  • the amount of each of these monomers can be determined by chromatographic methods, such as, for example, gas chromatography (GPC).
  • the amounts of each of the constituents can be measured by GPC by analysis as trimethylsilyl derivatives.
  • the sample can be prepared according to the following method: In a beaker, weigh 500 mg of sample and 50 mg of glucose pentaacetate (internal standard) of known purity. Add 50 ml of pyridine and stir until completely dissolved. Take 1 ml in a scoop, add 0.5 ml of bis- (trimethylsilyl) -trifluoroacetamide and heat for 40 minutes at 70 ° C.
  • DB1 column 30 m long and 0.32 mm in diameter with a film thickness of 0.25 ⁇ m
  • a type 1 injector 177 equipped with a focus liner with glass wool and heated to 300 ° C. using a split ratio of 30, the helium flow rate being 1.7 ml / min,
  • 1, 2 ⁇ of the sample can be introduced into the chromatograph, the column being heated from 100 ° C. to 320 ° C. with a ramp of 7 ° C./min and then a 15-minute stage at 15 ° C. 320 ° C.
  • (A1) is dimethylcarbonate isosorbide and (A2) dimers of (A1)
  • (A1) has a relative retention time of about 0.74
  • (A2) has a relative retention time ranging from about 1.34 to 1.79, the internal standard having a retention time of about 15.5 minutes.
  • the mass percentage of each of the constituents can be calculated by determining the area of the corresponding peaks and calculating, for each constituent, the ratio of the area of the peak corresponding to it to the total area of all the components. peaks (with the exception of the peak of the internal standard).
  • the monomer (A1) and / or the dimer (A2) reacts with the monomer (B1) and / or (B2) by a transesterification reaction, this reaction being conducted in a reactor.
  • This reaction can be carried out in the absence of catalyst.
  • a suitable catalyst makes it possible to accelerate the reaction and / or to increase the degree of polymerization of the polycarbonate thus formed during step (3).
  • the type and transesterification condensation conditions of step (3) are not particularly limited.
  • step (3) is advantageously in the presence of a known transesterification polycondensation catalyst, advantageously a catalyst comprising at least one alkali metal or alkaline earth metal ion, a quaternary ammonium ion, a quaternary phosphonium ion , a cyclic nitrogen compound, a basic boron compound or a basic phosphorus compound.
  • a known transesterification polycondensation catalyst advantageously a catalyst comprising at least one alkali metal or alkaline earth metal ion, a quaternary ammonium ion, a quaternary phosphonium ion , a cyclic nitrogen compound, a basic boron compound or a basic phosphorus compound.
  • a catalyst comprising at least one alkali metal ion mention may be made of cesium, lithium, potassium or sodium salts. These salts may in particular be carbonates, hydroxides, acetates, stearates, borohydrides, borides, phosphates, alcoholates or phenolates, as well as their derivatives.
  • the catalyst comprising at least one alkaline earth metal ion mention may be made of calcium, barium, magnesium or strontium salts. These salts may in particular be carbonates, hydroxides, acetates or stearates and their derivatives.
  • the basic compounds based on boron it is preferably salts of alkyl or phenyl boron derivatives such as tetraphenyl boron.
  • Catalysts comprising basic phosphorus compounds may be phosphines.
  • Catalysts comprising a quaternary ammonium ion are preferably hydroxides such as tetramethylammonium hydroxide.
  • Catalysts comprising a cyclic nitrogen compound are preferably triazole, tetrazole, pyrrole, pyrimidine, pyrazine, pyridazine, picoline, piperidine, pyridine, aminoquinoline or imidazole derivatives.
  • the catalyst is chosen from catalysts comprising at least one alkali metal ion, the catalysts comprising a cyclic nitrogen compound and catalysts comprising a quaternary ammonium ion, such as cesium carbonate, triazoles, tetramethylammonium hydroxide, most preferably cesium carbonate.
  • a quaternary ammonium ion such as cesium carbonate, triazoles, tetramethylammonium hydroxide, most preferably cesium carbonate.
  • the molar amount of catalyst, if any, relative to the amount of (A1) and (A2) is advantageously from 10-7% to 1%, preferably from 10-4% to 0.5%. Its amount can be adjusted depending on the catalyst used. By way of example, preferably from 10 "3 to 10 " 1 % of catalyst comprising at least one alkali metal ion is used.
  • additives such as stabilizers may be added to (A1) and / or (A2) and (B1) and / or (B2).
  • the stabilizer may be for example a phosphoric acid-based compound such as trialkyl phosphates, based on phosphorous acid such as phosphite derivatives or phosphates, or a salt of these acids, for example zinc salts; this stabilizer makes it possible to limit the coloration of the polymer during its manufacture. Its use can be advantageous especially when carrying out the melt polycondensation.
  • the amount of stabilizing agent is generally less than 0.01% of the total number of moles of (A1), (A2), (B1) and (B2).
  • the polycondensation step of (A1) and / or (A2) and (B1) and / or (B2) is carried out in step (3).
  • This reaction can be carried out in the molten state, that is to say by heating the reaction medium in the absence of a solvent.
  • This polymerization can also be carried out in the presence of a solvent.
  • This reaction is preferably carried out in the molten state.
  • Step (3) is performed for a time sufficient to obtain a polycarbonate.
  • the duration of step (3) ranges from 1 hour to 24 hours, for example from 2 to 12 hours.
  • At least part of step (3) of the process according to the invention can be carried out at a temperature ranging from 100 ° C. to 250 ° C., preferably from 150 ° to 235 ° C.
  • the reactor is thermoregulated during step (3) at a temperature ranging from 100 ° C to 250 ° C, preferably from 150 ° C to 235 ° C.
  • step (3) It is possible to conduct the whole of step (3) in isotherm. However, it is generally preferred to increase the temperature during this step, either in steps of temperature, either by using a temperature ramp. This increase in temperature during step (3) makes it possible to improve the degree of progress of the polycondensation reaction by transesterification and thus to increase the molecular weight of the polycarbonate finally obtained, the latter also having a lower coloring. than when the whole of step (3) of the process is carried out at its highest temperature.
  • step (3) it is of course preferred to carry out step (3) under an inert atmosphere, for example under nitrogen.
  • step (3) is carried out at a pressure ranging from 30 kPa to 1 10 kPa, advantageously from 50 to 105 kPa, preferably from 90 to 105 kPa, for example at atmospheric pressure.
  • a pressure ranging from 30 kPa to 1 10 kPa, advantageously from 50 to 105 kPa, preferably from 90 to 105 kPa, for example at atmospheric pressure.
  • at least half of the total duration of step (3) is performed at this pressure.
  • step (3) can be carried out during the entire duration or during a portion under a little more vacuum, for example with a pressure inside the reactor of between 100 Pa and 20 kPa.
  • this vacuum is regulated according to the temperature inside the reactor and the degree of polymerization: when the degree of polymerization is low, in case of too low pressure and too high temperature, the reaction can not be done correctly because the monomers are removed from the reactor by distillation.
  • This vacuum step a little further can be performed at the end of the reaction, which allows more than eliminate some of the residual species.
  • the reactor is generally equipped with a means for removing the alcohols generated during the transesterification polycondensation reaction, for example a distillation head connected to a condenser.
  • the reactor is generally equipped with a stirring means such as a blade stirring system.
  • the monomer (A1) and / or the dimer (A2) have the advantage of alternately reacting with the monomers (B1) and / or (B2) during step (3).
  • the reaction thus leads to an oligomer having an alternating architecture.
  • the process may be carried out discontinuously ("batch"), continuously, or semicontinuously semi-discontinuous manner.
  • the oligocarbonate formed during the process is recovered in step (4).
  • This oligocarbonate can be directly converted into granules by means of a granulator or in any other form. It is also possible to carry out a purification of the product thus obtained in a step subsequent to step (4), for example by dissolving the product in a solvent such as chloroform and then precipitating by adding a non-solvent such as methanol.
  • a mass yield defined by the ratio of the mass of oligocarbonate recovered on the mass of the sum of the monomers or dimers used, greater than or equal to 60%, advantageously greater than 70%, preferably greater than 80%.
  • the present invention also relates to an oligocarbonate polyol obtainable by the method according to the invention as defined above.
  • the oligocarbonate polyol according to the invention comprises a phenol content of less than 50 ppb.
  • the residual phenol content is measured by gas chromatography on a sample previously completely hydrolysed by acid hydrolysis.
  • Those skilled in the art can easily perform the acid hydrolysis of the oligocarbonates and analyze the reaction crude by gas chromatography with an internal standard to measure a quantitative response.
  • the oligocarbonate polyol obtained by the process according to the invention has a molar mass of less than 5000 g / mol and hydroxyl chain terminations.
  • the molar mass of the oligocarbonate can be decreased or increased respectively by decreasing, respectively increasing, the amount of monomers (B1) and / (B2) used in step (3) compared with that of (A1) and / or (A2).
  • the branching ratio of the oligocarbonate can be decreased or increased respectively by decreasing, respectively increasing, the amount of monomer (B2) used in step (3) compared with that of (B1).
  • the oligocarbonate polyol obtained by the process according to the invention also has an OH number greater than 100 mg KOH / g.
  • the subject of the present invention is also a method for preparing a polymeric material, characterized in that the oligocarbonate polyol according to the invention is reacted with a monomer having at least two functions each capable of reacting with a hydroxyl function.
  • the polyurethane material according to the invention may be especially intended for the preparation of an adhesive, a paint, a lacquer, a varnish or a resin, in particular a polyurethane resin.
  • the monomer having at least two functions each capable of reacting with a hydroxyl function is a polyisocyanate, in particular a diisocyanate.
  • the process according to the invention therefore leads to a polycarbonate urethane.
  • the monomer having at least two functions each capable of reacting with a hydroxyl function is a linear or cyclic aliphatic diisocyanate or an aromatic diisocyanate.
  • the present invention also relates to a polycarbonate obtainable by the above method, that is to say by reacting the oligocarbonate polyol according to the invention with a polyisocyanate, in particular a diisocyanate.
  • the polyisocyanate is a polyisocyanate or a mixture of polyisocyanates.
  • polyisocyanate is intended to mean a compound having a -NCO functionality of greater than or equal to 2.
  • polyisocyanate therefore notably includes diisocyanates having a functionality -NCO equal to 2, triisocyanates having a functionality of NCO equal to 3, as well as polyisocyanates having a -NCO functionality strictly greater than 2 and strictly less than 3.
  • aliphatic polyisocyanate is intended to mean a polyisocyanate which does not contain an aromatic ring.
  • the term aliphatic polyisocyanate therefore includes non-cyclic aliphatic polyisocyanates and cycloaliphatic polyisocyanates.
  • the polyisocyanate is an aliphatic polyisocyanate having a -NCO functionality strictly greater than 2, chosen in particular from a diisocyanate trimer, more particularly a diisocyanate isocyanurate or a diisocyanate biuret corresponding to the following formulas:
  • R is a C 4 -C 3 alkylene group, preferably an alkylene group in
  • C 4 -C 30 alkylene group means a divalent hydrocarbyl radical comprising 4 to 30 carbon atoms, saturated or partially saturated, linear, linear or branched, and which may comprise a ring aliphatic.
  • the aliphatic polyisocyanate having a -NCO functionality strictly greater than 2 is chosen from a pentamethylene diisocyanate trimer (PDI), a trimer of hexamethylene diisocyanate (HDI), a trimer of isophorone diisocyanate (IPDI ) or a mixture thereof; preferably an IPDI trimer or a PDI trimer.
  • PDI pentamethylene diisocyanate trimer
  • HDI hexamethylene diisocyanate
  • IPDI isophorone diisocyanate
  • the polyisocyanate is a non-cyclic aliphatic diisocyanate.
  • the non-cyclic aliphatic diisocyanate is chosen from pentamethylene diisocyanate (PDI), hexamethylene diisocyanate (HDI), isophorone diisocyanate (IPDI), methylene dicyclohexyl diisocyanate (hydrogenated HMDI or MDI) or a mixture thereof. ; more preferably NPDI.
  • the aromatic polyisocyanate is chosen from 1,3-phenylene diisocyanate, toluene-2,4-diisocyanate, toluene-2,6-diisocyanate and diphenyl-3,3'-dimethyl-4.
  • the polycarbonate according to the invention is characterized in that its molar mass is greater than 5000 g / mol.
  • the polycarbonate according to the invention has a bending stress at break greater than 1800 MPa as measured according to the ISO 178: 2010 standard. According to one embodiment, the polycarbonate according to the invention has an impact strength greater than 20 kJ / m 2 notched as measured according to the Charpy method DIN EN ISO 179: 2010.
  • the polycarbonate according to the invention does not break during a Charpy test in non-notched according to DIN EN ISO 179: 2010.
  • the polycarbonate according to the invention has an elongation at break in tension greater than 50% as measured according to the ISO 527-1: 2012 standard.
  • the thermal properties of the polyesters were measured by differential scanning calorimetry (DSC): The sample is first heated under a nitrogen atmosphere in an open crucible of 10 to 280 ° C (10 ° C.min -1 ). cooled to 10 ° C. (10 ° C.min -1 ) and then heated to 320 ° C. under the same conditions as the first step.
  • the glass transition temperatures (Tg) were taken at the midpoint of the second heater.
  • the possible melting temperatures are determined on the endothermic peak (onset of the peak) in the first heating. In the same way the determination of the enthalpy of fusion (area under the curve) is carried out at the first heating.
  • Mn it is determined by size exclusion chromatography in THF using polystyrene standards.
  • the sample is prepared by dissolution in THF at a concentration of 5 mg / ml.
  • the OH number is determined by 1 H NMR using a derivatization technique by adding trifluoroacetic anhydride and ⁇ , ⁇ , ⁇ -trifluorotoluene as internal standard.
  • Adhesion is measured according to ASTM Standard D3359-09. Mechanical properties
  • Bending test determination of the bending stress at break (ISO 178: 2010 standard).
  • Tensile test determination of elongation at break in tension (ISO 527-1: 2012).
  • Impact resistance determination of Charpy impact characteristics (DIN EN ISO 179-1: 2010 standard, not notched: ISO 179/1 eU or notched: ISO 179/1 eA).
  • Isosorbide dimethyl carbonate which is useful for the process for producing the polycarbonate diol oligomers according to the invention, is obtained according to the protocol described below.
  • the distillate obtained is a white solid containing 100% by weight of isosorbide dimethyl carbonate and contains no trace of dimers.
  • the molar ratio (A1) / (B1) is 0.9 to 1.
  • the amount of cesium carbonate is 17.1 mg (2.5 x 10 -4 mol).
  • the plant is placed under a nitrogen atmosphere and the reaction medium is heated by means of the heat transfer fluid.
  • the temperature is gradually raised to 65 ° C. so that the molten reaction medium is homogeneous and five "vacuum (300 mbar) -nitrogen (flow)" cycles are applied before continuing to increase the temperature.
  • the temperature rise between each level is in 15 minutes.
  • a first step takes place at a temperature of 100 ° C under a nitrogen flow of 5 ml / min of nitrogen for 2 hours.
  • the temperature is thereafter brought to 180 ° C in 15 minutes and a vacuum of 50 mbar is applied. This step lasts 3 hours.
  • the product is then cooled under nitrogen and poured into a pillbox when the temperature is around 60 ° C.
  • Examples 6 and 7 are synthesized from a variable diol (B1) (hexane diol or butane diol) and isosorbide.
  • DBTDL dibutyltin dilaurate
  • Example 8 Use of oligocarbonates polyols according to the invention, in the manufacture of thermosetting resins of the polyurethane (PU) type.
  • oligocarbonate polyol synthesized according to Example 3 50 grams of oligocarbonate polyol synthesized according to Example 3 is solubilized in 250 ml of acetone in which 6.3 mg of DBTDL and 12.33 grams of IPDI are added. The mixture is heated at 60 ° C. for 3 h and then the solvent is evaporated in a rotavapor and then in a vacuum oven for 24 hours at 60 ° C.
  • the Tg of the product obtained by DSC is 105 ° C.
  • the molar mass (Mn) of this polycarbonate is 12600 g / mol obtained by SEC in solvent THF with a polystyrene calibration.
  • the product obtained is then melted and poured into a mold to obtain test pieces for the study of the mechanical properties in bending and the evaluation of the impact resistance in Charpy.
  • the flexural modulus is 2030 MPa.
  • the notched tests show average values on 5 test pieces of 30 kJ / m 2 .

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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)
  • Polyesters Or Polycarbonates (AREA)
  • Polyurethanes Or Polyureas (AREA)
EP18796733.6A 2017-10-16 2018-10-15 Oligocarbonatpolyole aus dianhydrohexitol-dialkylcarbonat oder einem dimer von dianhydrohexitol-dialkylcarbonat, verfahren zu ihrer herstellung und ihre verwendung Pending EP3697828A1 (de)

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FR1759690A FR3072381B1 (fr) 2017-10-16 2017-10-16 Oligocarbonates polyols obtenus a partir de dialkylcarbonate de dinahydrohexitol ou un dimere de carbonate de dianhydrohexitol, leur procede de fabrication et leurs utilisations
PCT/FR2018/052558 WO2019077250A1 (fr) 2017-10-16 2018-10-15 Oligocarbonates polyols obtenus a partir de dialkylcarbonate de dinahydrohexitol ou un dimere de carbonate de dianhydrohexitol, leur procede de fabrication et leurs utilisations

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CN1319204C (zh) 2002-04-15 2007-05-30 日立麦克赛尔株式会社 离子传导性电解质及使用其的电池
DE10343471A1 (de) 2003-09-19 2005-05-12 Bayer Materialscience Ag Verfahren zur Herstellung von aliphatischen Oligocarbonatdiolen
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JP4560373B2 (ja) 2004-10-28 2010-10-13 旭化成ケミカルズ株式会社 末端に水酸基を有するポリカーボネート／ポリエーテルブロック共重合体
JP4560374B2 (ja) 2004-10-28 2010-10-13 旭化成ケミカルズ株式会社 水酸基末端を有するポリカーボネート／ポリエーテルブロック共重合体
WO2007148604A1 (ja) 2006-06-19 2007-12-27 Mitsubishi Chemical Corporation ポリカーボネート共重合体及びその製造方法
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JP6146961B2 (ja) * 2011-06-16 2017-06-14 三菱ケミカル株式会社 ポリカーボネートジオール含有組成物およびその製造方法、並びにポリカーボネートジオール含有組成物を用いたポリウレタン
JP6229250B2 (ja) 2012-09-21 2017-11-15 三菱ケミカル株式会社 ポリカーボネートジオール含有組成物及びポリカーボネートジオール含有組成物の製造方法
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JP2020537709A (ja) 2020-12-24
FR3072381A1 (fr) 2019-04-19
US20200325273A1 (en) 2020-10-15
US11299585B2 (en) 2022-04-12
KR102638491B1 (ko) 2024-02-21
JP7434160B2 (ja) 2024-02-20
KR20200062231A (ko) 2020-06-03
WO2019077250A1 (fr) 2019-04-25

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