WO2019175313A1 - Herstellungsverfahren von polyetherester elastomeren - Google Patents
Herstellungsverfahren von polyetherester elastomeren Download PDFInfo
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- WO2019175313A1 WO2019175313A1 PCT/EP2019/056423 EP2019056423W WO2019175313A1 WO 2019175313 A1 WO2019175313 A1 WO 2019175313A1 EP 2019056423 W EP2019056423 W EP 2019056423W WO 2019175313 A1 WO2019175313 A1 WO 2019175313A1
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- WIPO (PCT)
- Prior art keywords
- diols
- diamines
- group
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- block copolymer
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/91—Polymers modified by chemical after-treatment
- C08G63/914—Polymers modified by chemical after-treatment derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/916—Dicarboxylic acids and dihydroxy compounds
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/66—Polyesters containing oxygen in the form of ether groups
- C08G63/668—Polyesters containing oxygen in the form of ether groups derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/672—Dicarboxylic acids and dihydroxy compounds
-
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
- C08G63/785—Preparation processes characterised by the apparatus used
-
- 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
- C08G69/00—Macromolecular compounds obtained by reactions forming a carboxylic amide link in the main chain of the macromolecule
- C08G69/44—Polyester-amides
Definitions
- the present invention relates to a process for preparing a block copolymer comprising reacting at least one aromatic polyester having a melting point in the range of 160 to 350 ° C with at least one compound selected from the group consisting of diamines and diols at a temperature of greater 160 ° C to obtain a mixture (Ga); and annealing the mixture (Ga) at a temperature in the range of 100 to 300 ° C for a time in the range of 4 to 240 hours to obtain a block copolymer, wherein in step (a) the compound is selected from the group consisting of Diamines and diols in an amount of 0.02 to 0.3 moles per mole of ester bond in the polyester is used.
- the present invention furthermore relates to block copolymers obtained or obtainable by such a process and to the use of such block copolymers for the production of extruded, injection-molded and press articles and foams, foam particles, shoe soles, cable sheathings, hoses, profiles, drive belts, fibers, nonwovens, Films, molded parts, connectors, housings, damping elements for the electrical industry, the automotive industry, mechanical engineering, 3D printing, medicine and consumer goods.
- TPE thermoplastic elastomers
- EP 0 656 397 A1 discloses triblock polyaddition products comprising TPU blocks and polyester blocks which consist of two hard phase blocks, namely the polyester hard phase and the hard TPU phase, consisting of the urethane hard segment, the oligomeric or polymeric reaction product of an organic phase Diisocyanate and a low molecular weight chain extender, preferably an alkanediol and / or dialkylene glycol and the elastic urethane soft segment, consisting of the higher molecular weight polyhydroxyl compound, preferably a higher molecular weight polyester and / or polyether, which chemically linked together blockwise by urethane and / or amide bonds are.
- TPU blocks and polyester blocks which consist of two hard phase blocks, namely the polyester hard phase and the hard TPU phase, consisting of the urethane hard segment, the oligomeric or polymeric reaction product of an organic phase Diisocyanate and a low molecular weight chain extender, preferably an alkanediol and /
- the urethane or amide bonds are formed, on the one hand, from terminal hydroxyl or carboxyl groups of the polyesters and, on the other hand, from terminal isocyanate groups of the TPU.
- the reaction products may also have other bonds such as urea bonds, allopha- nates, isocyanurates and biurets.
- EP 1 693 394 A1 discloses thermoplastic polyurethanes with polyester blocks and processes for their preparation. In this case, thermoplastic polyesters are reacted with a diol and then the resulting reaction product reacted with isocyanates. In the processes known from the prior art, it is often difficult to adjust the block lengths and thus the properties of the obtained polymer
- this object is achieved by a process for the preparation of a block copolymer comprising the steps
- step (b) annealing the mixture (Ga) at a temperature in the range of 100 to 300 ° C for a time in the range of 1 to 240 hours to obtain a block copolymer, wherein in step (a) the compound is selected from the group consisting of diamines and diols in an amount ranging from 0.02 to 0.3 moles per mole of ester bond in the polyester.
- step (b) a molecular weight buildup is carried out by annealing under the conditions according to the invention.
- a block copolymer is understood as meaning a polymer which is composed of repeating blocks, for example of two repeating blocks.
- the process according to the invention comprises the steps (a) and (b).
- step (a) at least one aromatic polyester having a melting point in the range of 160 to 350 ° C is selected from at least one compound selected from the group consisting of diamines and diols at a temperature greater than 160 ° C to obtain a mixture (Ga ), wherein the compound selected from the group consisting of diamines and diols in an amount in the range of 0.02 to 0.3 moles per mole of ester bond in the polyester is used.
- the diols and diamines in the context of the present invention are preferably polymeric compounds.
- the reaction takes place at a temperature of greater than 160 ° C., in particular greater than 200 ° C.
- the temperature in the reaction according to step (a) is above the melting point of the polyester used.
- the amount of the compounds used in step (a) is preferably selected so that the molar amount of the amine and hydroxy groups used, based on the amount of ester bonds in the polyester in the range of 1: 3 to 1: 50, more preferably in Range from 1: 5 to 1:20, more preferably in the range from 1: 8 to 1: 12. Accordingly, becomes the compound selected from the group consisting of diamines and diols, for example, used in an amount in the range of 0.05 to 0.2 moles per mole of ester bond in the polyester, more preferably in an amount in the range of 0.1 to 0.15 moles per Mol ester bond in the polyester.
- the melting points or melting ranges are determined by means of DSC on predried samples. Unless otherwise stated, the DSC measurement is carried out at a heating rate of 20 ° C / min in a temperature range of 70 ° C to 250 ° C. The holding time at 250 ° C is 2 minutes, the cooling rate in the cooling is, unless otherwise stated, 20 ° C / min.
- the reaction according to step (a) takes place at a temperature of greater than 160 ° C., a mixture (G-a) being obtained.
- mixture (G-a) is tempered at a temperature in the range of 100 to 300 ° C for a time in the range of 1 to 240 hours to obtain a block copolymer.
- the temperature in the treatment according to step (b) in the context of the present invention is lower than the melting temperature of the mixture G-a or of the resulting block copolymer.
- step (b) of the process according to the invention is, for example, crystallization, postcrystallization or a solid-state reaction, such as solid-state polymerization or polycondensation in the solid phase.
- step (b) of the process according to the invention is carried out at a temperature which is below the melting point of the resulting mixture (G-a).
- Block copolymers of a high-melting polyester and a diol or diamine are prepared by the process according to the invention.
- the biphenyl block copolymer obtained according to the invention typically contains crystalline ester blocks and amorphous blocks, in particular amorphous polyol blocks which are coupled via amide, ester and / or urethane bonds, or else partially crystalline blocks.
- the reaction according to step (a) is preferably carried out continuously.
- the present invention accordingly relates to a process for the preparation of a block copolymer as described above, wherein the reaction according to step (a) takes place continuously.
- the reaction takes place at a temperature of over 160 ° C.
- the reaction can be carried out according to the invention in a suitable apparatus, the method suitable for the person skilled in the art being known per se.
- additives or auxiliaries are used to accelerate or to improve the reaction according to step (a).
- catalysts can be used.
- Suitable catalysts for the reaction according to step (a) are, for example, tributyltin oxide, tin (II) dioctoate, dibutyltin dilaurate or bi (III) carboxylates.
- reaction according to step (a) can be carried out in an extruder.
- reaction according to step (a) takes place in a kneader.
- reaction according to step (b) can be carried out in a solid-phase reactor, such as, for example, a vacuum oven or tumble reactor.
- the reaction according to step (a) can be carried out, for example, at a temperature in the range from 160 to 350 ° C., preferably in the range from 220 to 300 ° C. and in particular from 220 to 280 ° C., more preferably from 230 to 260 ° C.
- a residence time of 1 second to 15 minutes preferably with a residence time of 2 seconds to 10 minutes, more preferably with a residence time of 5 seconds to 5 minutes or with a residence time of 10 seconds to 1 minute in, for example, flowable, softened or preferably melted state of the polyester and of the polymer diol, in particular by stirring, rolling, kneading or, preferably, extrusion, for example using conventional plasticizing devices, such as mills, kneaders or extruders, preferably in an extruder.
- the present invention accordingly relates to a process for preparing a block copolymer as described above, wherein the reaction according to step (a) takes place in a stirred tank, reactor, extruder or a kneader.
- the method according to the invention may comprise further steps, for example temperature adjustments or shaping steps.
- the annealing according to step (b) takes place according to the invention at a temperature in the range from 100 to 300 ° C., preferably in the range from 150 to 200 ° C. and in particular from 160 to 200 ° C.
- the solid phase condensation takes place below the crystallization temperature of the resulting polymer.
- the annealing is carried out for a duration in the range of 1 to 240 hours, for example for a duration in the range of 4 to 120 hours, more preferably for a duration in the range of 8 to 48 hours.
- the annealing is carried out for a duration in the range of 1 to 48 hours or for a duration in the range of 1 to 24 hours.
- the present invention also relates to a process for preparing a block copolymer as described above, wherein the reaction according to step (b) takes place in a stirred tank, reactor, extruder or a kneader.
- the aromatic polyesters used according to the invention have a melting point in the range from 160 to 350.degree. C., preferably a melting point of greater than 180.degree.
- the polyesters suitable according to the invention have a melting point of greater than 200 ° C., particularly preferably a melting point of greater than 220 ° C.
- the polyesters suitable according to the invention particularly preferably have a melting point in the range from 220 to 350.degree.
- Polyesters useful in the present invention are known per se and contain at least one aromatic ring attached in the polycondensate backbone derived from an aromatic dicarboxylic acid.
- the aromatic ring may optionally also be substituted, for example by halogen atoms, e.g. Chlorine or bromine or / and by linear or branched alkyl groups having preferably 1 to 4 carbon atoms, in particular 1 to 2 carbon atoms, such as e.g. a methyl, ethyl, iso or n-propyl and / or an n, iso or tert-butyl group.
- the polyesters may be prepared by polycondensation of aromatic dicarboxylic acids or mixtures of aromatic and aliphatic and / or cycloaliphatic dicarboxylic acids and the corresponding ester-forming derivatives, e.g. Dicarboxylic anhydrides, mono- and / or diesters having expediently not more than 4 carbon atoms in the alcohol radical, with aliphatic dihydroxy compounds at elevated temperatures, for example from 160 to 260 ° C, in the presence or absence of esterification catalysts.
- aromatic dicarboxylic acids or mixtures of aromatic and aliphatic and / or cycloaliphatic dicarboxylic acids and the corresponding ester-forming derivatives
- Dicarboxylic anhydrides mono- and / or diesters having expediently not more than 4 carbon atoms in the alcohol radical
- aliphatic dihydroxy compounds at elevated temperatures, for example from 160 to 260 ° C, in the presence or absence of esterification catalysts.
- aromatic dicarboxylic acids for example naphthalenedicarboxylic acids, isophthalic acid and in particular terephthalic acid or mixtures of these dicarboxylic acids. If mixtures of aromatic and (cyclo) aliphatic dicarboxylic acids are used, up to 10 mol% of the aromatic dicarboxylic acids can be replaced by aliphatic and / or cycloaliphatic dicarboxylic acids with expediently 4 to 14 carbon atoms, such as e.g. Amber, adipic, azelaic, sebacic, dodecanedioic and / or cyclohexanedicarboxylic acid.
- Amber, adipic, azelaic, sebacic dodecanedioic and / or cyclohexanedicarboxylic acid.
- Suitable aliphatic dihydroxy compounds are preferably alkanediols having 2 to 6 carbon atoms and cycloalkanediols having 5 to 7 carbon atoms.
- alkanediols having 2 to 6 carbon atoms
- cycloalkanediols having 5 to 7 carbon atoms.
- polyesters are the polyalkylene terephthalates of alkanediols having 2 to 6 carbon atoms, in particular aromatic polyesters selected from the group consisting of polybutylene terephthalate (PBT), polyethylene terephthalate (PET) and polyethylene naphthalate (PEN), so that preferably polyethylene terephthalate and especially To find polybutylene terephthalate or mixtures of polyethylene terephthalate and polybutylene terephthalate application.
- PBT polybutylene terephthalate
- PET polyethylene terephthalate
- PEN polyethylene naphthalate
- the present invention accordingly relates to a process for preparing a block copolymer as described above, wherein the aromatic polyester is selected from the group consisting of polybutylene terephthalate (PBT), polyethylene terephthalate (PET) and polyethylene naphthalate (PEN).
- the present invention accordingly relates to a process for the preparation of a block copolymer as described above, wherein the aromatic polyester is polybutylene terephthalate (PBT).
- Suitable molecular weight ranges (Mn) of the polyester used according to the invention are in the range from 2000 to 100,000, more preferably in the range from 10,000 to 50,000.
- the determination of the weight-average molecular weights Mw of the thermoplastic block copolymers dissolved in HFIP (hexafluoroisopropanol) by means of GPC is carried out in the context of the present invention. Determination of the molecular weight is carried out by means of two series-connected GPC columns (PSS gel; 100A; 5m; 300 * 8mm, Jordi- Gel DVB; MixedBed; 5m 250 * 10mm; column temperature 60 ° C; flow 1 mL / min; RL Detector). The calibration is carried out with polymethyl methacrylate (EasyCal, PSS, Mainz), HFIP is used as eluent.
- step (a) the polyester is reacted with at least one compound selected from the group consisting of diamines and diols to obtain the mixture (G-a).
- Suitable diamines and diols are known per se to the person skilled in the art.
- low molecular weight or even oligomeric and polymeric diols and diamines can be used.
- the average molecular weight Mn of the diamine or diol used can be in the range from 200 to 2000 g / mol.
- the present invention accordingly relates to a process for preparing a block copolymer as described above, wherein the compound selected from the group consisting of diamines and diols has an average molecular weight Mn in the range of 200 to 2000 g / mol.
- the compound selected from the group consisting of diamines and diols has an average molecular weight Mn in the range of 200 to 2000 g / mol.
- a diol having an average molecular weight Mn in the range from 200 to 2000 g / mol it is also possible to use mixtures of different diols or different diamines.
- Suitable diols and diamines having an average molecular weight Mn in the range from 200 to 2000 g / mol are known per se to the person skilled in the art.
- polymer diamines or polymer diols are suitable in the context of the present invention.
- the present invention accordingly relates to a process for preparing a block copolymer as described above, wherein the compound selected from the group consisting of diamines and diols is a polymer diamine or a polymer diol.
- Suitable polymer diols are, for example, selected from the group consisting of polyetherols, polyester oils, polycarbonate alcohols, hybrid polyols and polysiloxanes.
- Polyols are generally known to the person skilled in the art and are described, for example, in "Kunststoffhandbuch, Volume 7, Polyurethanes", Carl Hanser Verlag, 3rd edition 1993, Chapter 3.1. Particular preference is given to using polyesteroie or polyetheroie as polyols. Particularly preferred are polyether polyols.
- the number-average molecular weight of the polyols used according to the invention is preferably between 200 and 2000 g / mol, for example between 250 g / mol and 2000 g / mol, preferably between 500 g / mol and 1500 g / mol, in particular between 650 g / mol and 1000 g / mol.
- Preferred polyetheroic polyethylenes according to the invention are polyethylene glycols, polypropylene glycols and polytetrahydrofurans, as well as their Mischpolyetheroie.
- the present invention accordingly relates to a process for preparing a block copolymer as described above, wherein the compound selected from the group consisting of diamines and diols is a polytetrahydrofuran.
- the polymer diol is a polytetrahydrofuran (PTHF) having a molecular weight Mn in the range from 200 g / mol to 2000 g / mol, more preferably in the range from 250 g / mol to 1500 g / mol, more preferably in Range from 500 g / mol to 1000 g / mol.
- PTHF polytetrahydrofuran
- polyethers are suitable in addition to PTHF, or even polyester.
- the present invention accordingly relates to a process for preparing a block copolymer as described above, wherein the polymer diol is a polyether diol. According to a further embodiment, the present invention accordingly relates to a process for preparing a block copolymer as described above, wherein the compound selected from the group consisting of diamines and diols is a polyether diol.
- the present invention also relates to a process
- the polyol can be used in pure form or in the form of a composition containing the polyol and at least one solvent. Suitable solvents are known per se to the person skilled in the art.
- a mixture (Ga) is obtained which, in addition to the reaction product, may also comprise unreacted polyester or unreacted polymer diol.
- the reaction product is present according to the invention as a mixture, wherein the individual molecules may be different, for example, in the distribution and the length of the polyester blocks.
- step (b) of the process according to the invention a molecular weight is increased and thus can be obtained by the novel process block copolymer with a good property profile.
- the block copolymers obtained by the process according to the invention have, for example, good thermal stability.
- the process according to the invention may comprise further steps, wherein preferably the process according to the invention does not comprise a reaction of the mixture (G-a) with an isocyanate.
- the present invention also relates to a block copolymer obtained or obtainable by a process according to the invention.
- the block copolymers of the invention usually have a hard phase of aromatic polyester and a soft phase.
- the block copolymers according to the invention have a good phase separation between the elastic soft phase and the rigid hard phase due to their predetermined block structure, which results from the structure of already polymeric and thus long-chain molecules such as a polytetrahydrofuran and a polybutylene terephthalate building block.
- This good phase separation manifests itself in a property known as high 'snappiness', which is difficult to characterize with physical methods.
- the processing of the resulting block copolymers can be carried out according to customary processes, for example on extruders, injection molding machines, blow molding, calenders, kneaders and presses.
- the block copolymers according to the invention are in particular for the production of extrusion, injection molded and press articles as well as foams, foam particles, shoe soles, Jardinummantelun- gene, hoses, profiles, drive belts, fibers, nonwovens, films, moldings , Plugs, housings, damping elements for the electrical industry, automotive industry, mechanical engineering, 3D printing, medicine and consumer goods.
- the present invention also relates to the use of a block copolymer or of a block copolymer according to the invention, obtained or obtainable by a process according to the invention for the production of extrusion, injection molding and press articles and foams, foam particles, shoe soles, cable sheathings, sleeves. surfaces, belts, fibers, nonwovens, foils, molded parts, connectors, housings, damping elements for the electrical industry, the automotive industry, mechanical engineering, 3D printing, medicine and consumer goods.
- a process for producing a block copolymer comprising the steps
- step (b) annealing the mixture (Ga) at a temperature in the range of 100 to 300 ° C for a time in the range of 1 to 240 hours to obtain a block copolymer, wherein in step (a) the compound is selected from the group consisting of diamines and diols in an amount of 0.02 to 0.3 moles per mole of ester bond in the polyester is used.
- step (a) takes place in a stirred tank, reactor, extruder or kneader.
- a process for producing a block copolymer comprising the steps
- step (b) annealing the mixture (Ga) at a temperature in the range of 100 to 300 ° C for a time in the range of 1 to 240 hours to obtain a block copolymer, wherein in step (a) the compound is selected from the group consisting of diamines and diols in an amount of 0.02 to 0.3 moles per mole of ester bond in the polyester is used.
- aromatic polyester is selected from the group consisting of polybutylene terephthalate (PBT), polyethylene terephthalate (PET) and polyethylene naphthalate (PEN).
- PBT polybutylene terephthalate
- PET polyethylene terephthalate
- PEN polyethylene naphthalate
- the compound selected from the group consisting of diamines and diols is a polymer diamine or a polymer diol.
- Block copolymer obtained or obtainable according to a method according to any one of embodiments 1 to 16.
- a block copolymer obtained or obtainable according to a process for producing a block copolymer comprising the steps
- step (b) annealing the mixture (Ga) at a temperature in the range of 100 to 300 ° C for a time in the range of 1 to 240 hours to obtain a block copolymer, wherein in step (a) the compound is selected from the group consisting of diamines and diols in an amount of 0.02 to 0.3 moles per mole of ester bond in the polyester is used.
- a block copolymer obtained or obtainable according to a process for producing a block copolymer comprising the steps
- step (b) annealing the mixture (Ga) at a temperature in the range of 100 to 300 ° C for a time in the range of 1 to 240 hours to obtain a block copolymer, wherein in step (a) the compound is selected from the group consisting of diamines and diols in an amount of 0.02 to 0.3 moles per mole of ester bond in the polyester is used.
- step (a) the compound is selected from the group consisting of diamines and diols in an amount of 0.02 to 0.3 moles per mole of ester bond in the polyester is used.
- Polyol 1 Polybutylene terephthalate (PBT) having a weight-average molecular weight of 60,000 g / mol
- Polyol 2 polyether polyol having an OH number of 453.4, a weight-average molecular weight of 248 g / mol and excluding primary OH groups (based on tetramethylene oxide, functionality: 2)
- Polyol 3 Polyetherpolyol having an OH number of 1 12.2, a weight-average molecular weight of 1000 g / mol and excluding primary OH groups (based on tetramethylene oxide, functionality: 2)
- polyester (polyol 1) is melted in a DSM mini extruder at 260 ° C and reacted for 10 minutes with another polyol (polyol 2 or 3) (Table 1).
- Mixture is discharged and then annealed under nitrogen atmosphere in an oven at 170 ° C for 32 h.
- the molecular weight was determined by gel permeation chromatography. The number and weight average molecular weights obtained and the polydispersity after the reaction and after the annealing are shown in Table 2.
- Table 2 Number and weight average molecular weight after reaction and after annealing measurement method
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
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JP2020548917A JP2021515839A (ja) | 2018-03-14 | 2019-03-14 | ポリエーテルエステルエラストマーの製造方法 |
EP19709521.9A EP3765548A1 (de) | 2018-03-14 | 2019-03-14 | Herstellungsverfahren von polyetherester elastomeren |
CN201980015623.7A CN111788249A (zh) | 2018-03-14 | 2019-03-14 | 聚醚酯弹性体的制备方法 |
KR1020207029491A KR20200132939A (ko) | 2018-03-14 | 2019-03-14 | 폴리에테르 에스테르 엘라스토머의 제조 방법 |
US16/979,740 US20210040255A1 (en) | 2018-03-14 | 2019-03-14 | Production process for polyether ester elastomers |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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EP18161735 | 2018-03-14 | ||
EP18161735.8 | 2018-03-14 |
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WO2019175313A1 true WO2019175313A1 (de) | 2019-09-19 |
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PCT/EP2019/056423 WO2019175313A1 (de) | 2018-03-14 | 2019-03-14 | Herstellungsverfahren von polyetherester elastomeren |
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US (1) | US20210040255A1 (de) |
EP (1) | EP3765548A1 (de) |
JP (1) | JP2021515839A (de) |
KR (1) | KR20200132939A (de) |
CN (1) | CN111788249A (de) |
TW (1) | TW201938636A (de) |
WO (1) | WO2019175313A1 (de) |
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TWI829246B (zh) * | 2022-07-15 | 2024-01-11 | 匯智綠材科技股份有限公司 | 發泡材料組成物及發泡材料與其製作方法 |
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EP0656397A1 (de) | 1993-12-02 | 1995-06-07 | Elastogran GmbH | Temperaturbeständige, hochelastische, abriebfeste Polyurethan-Polyester-Triblockpolyadditionsprodukte, ein Verfahren zu ihrer Herstellung und ihre Verwendung |
EP1693394A1 (de) | 2001-08-10 | 2006-08-23 | Basf Aktiengesellschaft | Thermoplastische Polyurethane |
DE102009020211A1 (de) * | 2009-05-07 | 2010-11-11 | Basf Se | Verwendung eines Polyesters zur Herstellung von Formteilen mit einem niedrigen Gehalt an extrahierbaren Verbindungen |
WO2017144492A1 (de) * | 2016-02-22 | 2017-08-31 | Basf Se | Verfahren zur herstellung eines diblockcopolymers |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
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DE102004023105A1 (de) * | 2004-05-11 | 2005-12-08 | Zimmer Ag | Verfahren zur Herstellung von elastomeren Copolyestern |
CN101636427A (zh) * | 2006-01-27 | 2010-01-27 | 沙伯基础创新塑料知识产权有限公司 | 衍生自聚对苯二甲酸乙二醇酯的共聚醚酯 |
CN104371094B (zh) * | 2014-10-31 | 2016-06-08 | 中国科学院宁波材料技术与工程研究所 | 高性能聚醚酯弹性体的两步投料合成法 |
CN104693447A (zh) * | 2015-03-10 | 2015-06-10 | 苏州大学 | 一种聚醚酯多嵌段交替共聚物的制备方法 |
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2019
- 2019-03-14 US US16/979,740 patent/US20210040255A1/en not_active Abandoned
- 2019-03-14 CN CN201980015623.7A patent/CN111788249A/zh active Pending
- 2019-03-14 WO PCT/EP2019/056423 patent/WO2019175313A1/de active Search and Examination
- 2019-03-14 KR KR1020207029491A patent/KR20200132939A/ko unknown
- 2019-03-14 EP EP19709521.9A patent/EP3765548A1/de not_active Withdrawn
- 2019-03-14 JP JP2020548917A patent/JP2021515839A/ja active Pending
- 2019-03-14 TW TW108108547A patent/TW201938636A/zh unknown
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EP1693394A1 (de) | 2001-08-10 | 2006-08-23 | Basf Aktiengesellschaft | Thermoplastische Polyurethane |
DE102009020211A1 (de) * | 2009-05-07 | 2010-11-11 | Basf Se | Verwendung eines Polyesters zur Herstellung von Formteilen mit einem niedrigen Gehalt an extrahierbaren Verbindungen |
WO2017144492A1 (de) * | 2016-02-22 | 2017-08-31 | Basf Se | Verfahren zur herstellung eines diblockcopolymers |
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"Kunststoffhandbuch, Band 7, Polyurethane", vol. 7, 1993, CARL HANSER VERLAG |
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JP2021515839A (ja) | 2021-06-24 |
US20210040255A1 (en) | 2021-02-11 |
TW201938636A (zh) | 2019-10-01 |
CN111788249A (zh) | 2020-10-16 |
EP3765548A1 (de) | 2021-01-20 |
KR20200132939A (ko) | 2020-11-25 |
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