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
  • C08G64/04—Aromatic 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
  • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
  • C08G63/64—Polyesters containing both carboxylic ester groups and carbonate 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
  • C08G64/00—Macromolecular compounds obtained by reactions forming a carbonic ester link in the main chain of the macromolecule
  • C08G64/20—General preparatory processes
• • 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

Definitions

• This invention relates to a method of preparing polyestercarbonates. More particularly the method relates to a method of preparing polyestercarbonates in which diacids rather than diesters are employed as starting materials and said diacids are incorporated into the polyestercarbonate backbone with a high level of efficiency.
• Polyestercarbonates based on aliphatic diacids and aromatic bisphenols are known, commercially useful materials which are currently prepared under interfacial polymerization conditions comprising reaction of a mixture of a bisphenol such as bisphenol A (BPA) together with a dicarboxylic acid such as dodecandioic acid with phosgene in the presence of a solvent and an aqueous solution of an acid acceptor such as sodium hydroxide.
• BPA bisphenol A
• SP polycarbonate which typifies such polyestercarbonates is a copolymer of BPA ( ⁇ 92 mole %) and dodecanedioic acid (DDDA) ( ⁇ 8 mole%) and is available from GE Plastics, Mt Vernon, Indiana.
• solvent removal is typically carried out by introducing steam into a solution of the product polyestercarbonate, a process which can result in fusion of the isolated powder resin owing to the presence of solvent and the inherently lower glass transition temperatures of polyestercarbonates incorporating comonomer such as DDDA relative to the corresponding homopolycarbonates. Therefore only high molecular weight material can be manufactured this way.
• the present invention provides a method for the preparation of polyestercarbonates, said method comprising preparing a mixture comprising at least one activated diaryl carbonate, at least one dihydroxy aromatic compound, at least one diacid, at least one melt polymerization catalyst and optionally one or more co-catalysts, and heating under melt polymerization conditions to afford a product polyestercarbonate.
• the method further relates to the preparation of polycarbonate esters having a high level of polymer endcapping.
• melt polycarbonate refers to a polycarbonate made by the transesterification of a diaryl carbonate with a dihydroxy aromatic compound.
• BPA is herein defined as bisphenol A or 2,2-bis(4-hydroxyphenyl)propane.
• Catalyst system refers to the catalyst or catalysts that catalyze the transesterification of the bisphenol with the diaryl carbonate in the melt process.
• Catalytically effective amount refers to the amount of the catalyst at which catalytic performance is exhibited.
• aliphatic radical refers to a radical having a valence of at least one comprising a linear or branched array of atoms which is not cyclic.
• the array may include heteroatoms such as nitrogen, sulfur and oxygen or may be composed exclusively of carbon and hydrogen.
• aliphatic radicals include methyl, methylene, ethyl, ethylene, hexyl, hexamethylene and the like.
• aromatic radical refers to a radical having a valence of at least one comprising at least one aromatic group.
• aromatic radicals include phenyl, pyridyl, furanyl, thienyl, naphthyl, phenylene, and biphenyl.
• the term includes groups containing both aromatic and aliphatic components, for example a benzyl group.
• cycloaliphatic radical refers to a radical having a valance of at least one comprising an array of atoms which is cyclic but which is not aromatic.
• the array may include heteroatoms such as nitrogen, sulfur and oxygen or may be composed exclusively of carbon and hydrogen.
• cycloaliphatic radicals include cyclcopropyl, cyclopentyl cyclohexyl, tetrahydrofuranyl and the like.
• BMSC activated diaryl carbonate bis(methyl salicyl) carbonate
• the present invention provides a method for preparing polyestercarbonates by reacting under melt polymerization conditions at least one activated diaryl carbonate with at least one dihydroxy aromatic compound and at least one diacid in the presence of a catalytically effective amount of at least one melt polymerization catalyst and optionally one or more co-catalyst.
• the activated diaryl carbonate used according to the method of the present invention is "activated" in the sense that it undergoes transesterification reaction under melt polymerization conditions with a dihydroxy aromatic compound at a rate faster than the rate of the corresponding reaction of diphenyl carbonate.
• Activated diaryl carbonates thus encompass diaryl carbonates substituted with one or more electronegative substitutents such as halogen, cyano, perhaloalky, nitro, acyl and the like.
• activated diaryl carbonates for use according to the method of the present invention include bis(2-acetylphenyl) carbonate, bis(4-acetylphenyl) carbonate, bis(2-pivaloylphenyl) carbonate, bis(4-pivaloylphenyl) carbonate, bis(2- cyanophenyl) carbonate, bis(4-cyanophenyl) carbonate, bis(2-chlorophenyl) carbonate, bis(4-chlorophenyl) carbonate, bis(2, 4-dichlorophenyl) carbonate, bis(2, 4, 6- trichlorophenyl) carbonate, bis(2-nitrophenyl) carbonate, bis(4-nitrophenyl) carbonate, bis(2-fluorophenyl) carbonate, bis(2, 4-difluorophenyl) carbonate, bis(2, 4, 6- trifluorophenyl) carbonate, bis(2-trifluoromethylphenyl) carbonate, bis(4- trifluor
• R 1 and R 2 are independently Ci - C 20 alkyl radicals, C -C 2 o cycloalkyl radicals or C 4 -C 20 aromatic radicals, R and R are independently at each occurrence a halogen atom, cyano group, nitro group, Ci - C20 alkyl radical, C 4 -C 2 o cycloalkyl radical, C 4 -C 2 o aromatic radical, Ci - C20 alkoxy radical, C 4 -C 2 o cycloalkoxy radical, C 4 -C 2 o aryloxy radical, Ci - C20 alkylthio radical, C -C 2 o cycloalkylthio radical, C 4 - C 20 arylthio radical, Ci - C 20 alkylsulfinyl radical, C -C 2 o cycloalkylsulfinyl radical, C 4 -C 2 o arylsulfmyl radical, Ci - C20 alkyls
• activated diaryl carbonates having structure I include bis(methyl salicyl) carbonate (BMSC), bis(ethyl salicyl) carbonate, bis(propyl salicyl) carbonate, bis(butyl salicyl) carbonate, bis(benzyl salicyl) carbonate, and bis(methyl 4- chlorosalicyl) carbonate.
• BMSC bis(methyl salicyl) carbonate
• ethyl salicyl bis(ethyl salicyl) carbonate
• bis(propyl salicyl) carbonate bis(butyl salicyl) carbonate
• bis(benzyl salicyl) carbonate bis(methyl 4- chlorosalicyl) carbonate.
• BMSC bis(methyl salicyl) carbonate
• the dihydroxy aromatic compound used according to the method of the present invention is typically selected from the group consisting of bisphenols having structure II,
• R 5 -R 12 are independently a hydrogen atom, halogen atom, nitro group, cyano group, C1-C20 alkyl radical C .C2o cycloalkyl radical, or C 6 -C2 0 aryl radical;
• W is a bond, an oxygen atom, a sulfur atom, a SO2 group, a C 6 -C 2 o aromatic radical, a C -C 2 o cycloaliphatic radical or the group
• R ⁇ and R 14 are independently a hydrogen atom, C1-C20 alkyl radical, C 4 -C 2 o cycloalkyl radical, or G1-C2 0 aryl radical; or R 13 and R 14 together form a C 4 .C 2 o cycloaliphatic ring which is optionally substituted by one or more C1-C 20 alkyl, C 6 .C2o aryl, C 5 .C 21 aralkyl, C 5 -C 20 cycloalkyl groups or a combination thereof; dihydroxy benzenes having structure III
• R 15 is independently at each occurrence a halogen atom, nitro group, cyano group, C 1 -C2 0 alkyl radical, C 4 .C 2 o cycloalkyl radical C -C 2 o aryl radical; and d is an integer from 0 to 4;
• R 16 , R 17 , R 18 and R 19 are independently at each occurrence a halogen atom, nitro group, cyano group, C1-C 20 alkyl radical, C 4 .C 2 o cycloalkyl radical C 4 -C 2 o aryl radical; e and f are integers of from 0 to 3, g is an integer from 0 to 4, and h is an integer from 0 to 2.
• bisphenols having structure II examples include 2,2-bis(4-hydroxyphenyl)propane (bisphenol A); 2,2-bis(3-methyl-4-hydroxyphenyl)propane; l ,l -bis(4- hydroxyphenyl)cyclohexane; 1 ,1 -bis(4-hydroxyphenyl)-3,3,5-trimethylcyclohexane; 1 ,3-bis(2-(4-hydroxyphenyl)-2-propyl)benzene; 1 ,4-bis(2-(4-hydroxyphenyl)-2- propyl)benzene; and 1 ,4-bis(2-(4-hydroxy-3-methylphenyl)-2-propyl)benzene.
• bisphenol A 2,2-bis(4-hydroxyphenyl)propane
• bisphenol A 2,2-bis(3-methyl-4-hydroxyphenyl)propane
• l ,l -bis(4- hydroxyphenyl)cyclohexane 1 ,1 -bis(
• dihydroxy benzenes having structure III examples include hydroquinone, resorcinol, methylhydroquinone, phenylhydroquinone, 4-phenylresorcinol, and 4- methylresorcinol.
• dihydroxy naphthalenes having structure IV examples include 2,6-dihydroxy naphthalene; 2,6-dihydroxy-3-methyl naphthalene; 2,6-dihydroxy-3-phenyl naphthalene and of 2,8-dihydroxy naphthalene.
• dihydroxy naphthalenes having structure V examples include 1 ,4-dihydroxy naphthalene; 1 ,4-dihydroxy-2-methyl naphthalene; 1 ,4-dihydroxy-2-phenyl naphthalene and 1 ,3-dihydroxy naphthalene.
• the diacid may be an aromatic diacid such as 2,6-nathalene dicarboxylic acid, an aliphatic diacid such as succinic acid, or a cycloaliphatic diacid such as 1 ,7- cyclododecanedioic acid.
• the diacid employed is a diacid having structure VI
• R is a C 4 -C 3 o aromatic radical, a C ⁇ -C 40 aliphatic radical, or a C5-C30 cycloaliphatic radical.
• diacids having structure VI include terephthalic acid; isophthalic acid;l ,4-cyclohexanediacrboxylic acid; hexanedioic acid; octanedioic acid; decanedioic acid; dodecanedioic acid; tetradecanedioic acid; hexadecanedioic acid; octadecanedioic acid; cis 9-octenedioic acid; alpha- nonyldecanedioic acid; alpha-octylundecanedioic acid; and hydrogenated dimer acid. Dodecanedioic acid is frequently preferred.
• the melt polymerization catalyst used according to the method of the present invention may be any of a wide variety of transesterifcation catalysts capable of effecting reaction between the activated diaryl carbonate, the aromatic dihydroxy compound and the diacid present in the reaction mixture.
• the melt polymerization catalyst may be a single compound or a mixture of compounds and may be employed in combination with one or more co-catalysts such as quaternary ammonium salts or quaternary phosphonium salts.
• metal hydroxides such as alkali metal hydroxides and alkaline earth metal hydroxides are well adapted to serve as melt polymerization catalysts, although a variety of other catalysts are well suited to this task.
• alkaline earth metal hydroxides include lithium hydroxide, sodium hydroxide, potassium hydroxide, and mixtures thereof.
• alkaline earth metal hydroxides include calcium hydroxide, barium hydroxide, and mixtures thereof.
• melt polymerization catalysts which may be used advantageously according to the method of the present invention include alkali metal salts of carboxylic acids, alkaline earth metal salts of a carboxylic acids, and mixtures thereof.
• Alkali metal salts of carboxylic acids include lithium acetate, sodium benzoate, and dipotassium dodecanedioate.
• alkaline earth metal salts of a carboxylic acids include calcium benzoate, calcium adipate, and barium acetate.
• the catalyst used according to the method of the present invention may the salt of a polycarboxyic acid such a tetrasodium ethylenediamine tetracarboxylate, or disodium magnesium ethylenediamine tetracarboxylate.
• salts of polycarboxylic acids comprising a variety of metal cations may be employed as the melt polymerization catalyst according to the method of the present invention, disodium magnesium ethylenediamine tetracarboxylate serving as an example of a salt of a polycarboxylic acid comprising both alkali metal and alkaline earth metal cations.
• the melt polymerization catalyst comprises the salt of a non-volatile acid.
• non-volatile it meant that the acid from which the catalyst is made has no appreciable vapor pressure under melt polymerization conditions.
• non-volatile acids include phosphorous acid, phosphoric acid, sulfuric acid, and metal "oxo acids” such as the oxo acids of germanium, antimony, niobium and the like.
• Salts of non-volatile acids useful as melt polymerization catalysts according to the method of the present invention include alkali metal salts of phosphites; alkaline earth metal salts of phosphites; alkali metal salts of phosphates; alkaline earth metal salts of phosphates, alkali metal salts of sulfates, alkaline earth metal salts of sulfates, alkali metal salts of metal oxo acids, and alkaline earth metal salts of metal oxo acids.
• salts of nonvolatile acids include NaH 2 PO 3 , NaH 2 PO 4 , Na 2 H 2 PO 3 , KH 2 PO 4 , CsH 2 PO , Cs 2 H 2 PO 4 , Na 2 SO 4 , NaHSO 4 , NaSbO 3 , LiSbO 3 , KSbO 3 , Mg(SbO ) 2 , Na 2 GeO 3 , K 2 GeO 3 , Li2GeO 3 , Mg GeO 3 , Mg 2 GeO , and mixtures thereof
• the melt polymerization catalyst is employed in an amount equivalent to between about 1.0 x 10 "8 and about 1 x 10 "3 , preferably between about 1.0 x 10 "8 and about 1 x 10 "5 moles of melt polymerization catalyst per mole of dihydroxy aromatic compound.
• the method of the present invention may be practiced using a co- catalyst.
• the co-catalyst is a quaternary ammonium salt or quaternary phosphonium salt and is used in an amount corresponding to about 10 to about 250 times the molar amount of melt polymerization catalyst used.
• the catalyst and co- catalyst may be added to the reaction mixture either simultaneously, or the catalyst and co-catalyst may be added separately at different stages of the polymerization reaction.
• R 2 ' -R 24 are independently a C ⁇ -C o alkyl radical, C .C2o cycloalkyl radical or a C -C 20 aryl radical and X ⁇ is an organic or inorganic anion.
• the anion X " is typically an anion selected from the group consisting of hydroxide, halide, carboxylate, phenoxide, sulfonate, sulfate, carbonate, and bicarbonate.
• Examples of quaternary ammonium salts having structure VII include tetramethylammonium hydroxide, tetrabutylammonium acetate and the like.
• a quaternary phosphonium co- catlayst is employed, said co-catalyst having structure VIII
• R 25 -R 28 are independently a C
• the anion X " is typically an anion selected from the group consisting of hydroxide, halide, carboxylate, phenoxide, sulfonate, sulfate, carbonate, and bicarbonate.
• Examples of quaternary phosphonium salts having structure VIII include tetramethylphsophonium hydroxide, tetrabutylphosphonium acetate, tetrabutylphosphonium hydrogen carbonate, and the like.
• X " is a polyvalent anion such as carbonate or sulfate it is understood that the positive and negative charges in structures VII and VIII are properly balanced.
• R 25 -R 28 in structure VIII are each butyl groups and X ⁇ represents a carbonate anion, it is understood that X " represents Vi (CO 3 2 ).
• the reactants are employed according to the method of the present invention such that the molar ratio of activated diaryl carbonate to the total moles of aromatic dihydroxy compound and diacid is in a range between about 1.01 and about 2, preferably between about 1.01 and about 1.5, and still more preferably between about 1.01 and about 1.2.
• the molar ratio of activated diaryl carbonate to aromatic dihydroxy compound and diacid is 2 to 1.
• the amount of dicarboxylic acid employed is a range between about 0.01 about 0.10 moles of dicarboxylic acid per mole of aromatic dihydroxy compound employed.
• the reaction conditions of the melt polymerization are not particularly limited and may be conducted under a wide range of operating conditions.
• the term "melt polymerization conditions" will be understood to mean those conditions necessary to effect reaction between the activated diaryl carbonate, the dihydroxy aromatic compound, and the diacid of the present invention to afford a polyestercarbonate having sufficiently high molecular weight to possess useful polymer properties.
• the product polyestercarbonate has useful polymer properties when it possesses a weight average molecular weight of about 18,000 daltons or greater.
• the reaction temperature is typically in the range from about 150°C to about 330°C, and preferably from about 170°C to about 280°C.
• the pressure may be at atmospheric pressure, supraatmospheric pressure, or a range of pressures from atmospheric pressure to about 15 torr in the initial stages of the reaction, and at a reduced pressure at later stages, for example in the range of about 0.01 to about 15 torr.
• the reaction time is generally about 0.1 hours to about 10 hours.
• reactants bis(methyl salicyl) carbonate, bisphenol A and dicarboxylic acid having structure VI are heated under melt polymerization conditions for a period of between about 0.1 and about 10 hours to a temperature in a range between about 150°C and about 310°C at a pressure in a range between about atmospheric pressure and about 0.01 torr, in the presence of a melt polymerization catalyst, said melt polymerization catalyst being present in an amount corresponding to between about 1.0 x 10 " and about 1 x 10 "" moles per mole of bisphenol A, and a co-catalyst, said co-catalyst being present in an amount corresponding to between about 10 times and about 250 times the number of moles of melt polymerization catalyst.
• the method of the present invention may be practiced in either a continuous or batch mode and may be conducted in stages, for example an initial oligomerization stage followed by a separate stage in which the initially formed oligomers are converted to higher molecular weight product.
• the method of the present invention is not particularly limited with respect to the reaction equipment employed. Any reactor, batch or continuous, capable of melt mixing the polymerization mixture and removing volatile side products may be used. Because of their high efficiency continuous reactors are preferred
• M n number average
• M w weight average
• Terminal hydroxy groups first de ⁇ vatized with dioxaphospholanyl chloride and then measured by T l i P-NMR. Inco ⁇ oration of the diacid was measured by ⁇ -NMR.
• the pressure of the reaction vessel was controlled by means of a vacuum pump coupled to a nitrogen bleed
• the pressure within the reactor was measured with an MKS pira gauge.
• Ethylene diamine tetraaceticacid magnesium disodium salt Alfa-Aesar, 1 x 10 "6 mole per mole bisphenol A
• tetrabutyl phosphonium acetate Sachem, 2.5 x 10 "4 mole per mole bisphenol A
• the reactor was charged at ambient temperature and pressure with solid bisphenol A (General Electric Plastics Japan Ltd., 0.0.6570 mol), solid bis(methyl salicyl) carbonate (0.721 1 mol) and 12.1 lg of dodecanedioic acid (0.0526 mol).
• the catalyst was then injected into the bisphenol A layer and the reactor assembled.
• the reactor was then evacuated briefly and nitrogen was reintroduced. This step was repeated three times.
• the reactor was then lowered into the sand bath maintained at 170°C. After a five minute period stirring at 250 rpm was initiated. The pressure was lowered to 250 mmHg and the temperature was ramped to 240°C over 25 minutes.
• Example 2 was carried out as in Example 1. Comparative Examples 1 and 2 (CE-1 and CE-2) were carried out as described in Example 1 with the exception that diphenyl carbonate (DPC) was used as the carbonate source instead of bis(methyl salicyl) carbonate (BMSC). Data are gathered in Table 1 for polyestercarbonates prepared according to the method of the present invention (Examples 1 and 2) and for polyestercarbonates prepared using diphenyl carbonate (Comparative Examples 1 and 2). The column headings "Diacid” and "DAC” refer to the diacid comonomer and the diaryl carbonate used in the polymerization respectively.
• DPC diphenyl carbonate
• BMSC bis(methyl salicyl) carbonate
• % Inco ⁇ oration refers to percentage of the diacid actually inco ⁇ orated into the polymer backbone during the polymerization and the percentage of chain terminal groups in the product polymer which were not hydroxy groups.
• a polycarbonate prepared by a process comprising the melt reaction of a bisphenol with a diaryl carbonate will possess chain terminal groups which are hydroxy groups or which are aryloxy groups derived from the diaryl carbonate.
• the data in Table 1 reveal higher levels of diacid inco ⁇ oration in the product polyestercarbonate prepared according to the method of the present invention than are obtained using an alternate method relying on diphenyl carbonate.
• the data also reveal that the method of the present invention affords polyestercarbonates having a higher level of "endcapping" than is available using the alternate method employing diphenyl carbonate.

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