WO2003045550A1 - Catalyseur et procede de preparation d'un ester - Google Patents

Catalyseur et procede de preparation d'un ester Download PDF

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WO2003045550A1
WO2003045550A1 PCT/GB2002/005281 GB0205281W WO03045550A1 WO 2003045550 A1 WO2003045550 A1 WO 2003045550A1 GB 0205281 W GB0205281 W GB 0205281W WO 03045550 A1 WO03045550 A1 WO 03045550A1
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acid
alkyl
catalyst composition
reaction
acids
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PCT/GB2002/005281
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Charles Mark Lindall
John Ridland
Neville Slack
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Johnson Matthey Plc
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Priority to AU2002349116A priority Critical patent/AU2002349116A1/en
Publication of WO2003045550A1 publication Critical patent/WO2003045550A1/fr

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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1845—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing phosphorus
    • B01J31/185—Phosphites ((RO)3P), their isomeric phosphonates (R(RO)2P=O) and RO-substitution derivatives thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0201—Oxygen-containing compounds
    • B01J31/0211—Oxygen-containing compounds with a metal-oxygen link
    • B01J31/0212—Alkoxylates
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208—Oxygen, e.g. acetylacetonates
    • B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • B01J31/223—At least two oxygen atoms present in one at least bidentate or bridging ligand
    • 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
    • C08G63/82—Preparation processes characterised by the catalyst used
    • C08G63/84—Boron, aluminium, gallium, indium, thallium, rare-earth metals, or compounds thereof
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
    • C08G63/78—Preparation processes
    • C08G63/82—Preparation processes characterised by the catalyst used
    • C08G63/85—Germanium, tin, lead, arsenic, antimony, bismuth, titanium, zirconium, hafnium, vanadium, niobium, tantalum, or compounds thereof
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/30—Complexes comprising metals of Group III (IIIA or IIIB) as the central metal
    • B01J2531/31—Aluminium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/40—Complexes comprising metals of Group IV (IVA or IVB) as the central metal
    • B01J2531/46—Titanium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/40—Complexes comprising metals of Group IV (IVA or IVB) as the central metal
    • B01J2531/48—Zirconium

Definitions

  • the invention concerns catalyst compositions and in particular catalyst compositions which comprise novel organotitanium, organozirconium or organoaluminium compounds containing phosphorous which are useful catalysts for esterification reactions.
  • Organotitanium compounds and, in particular, titanium alkoxides or alkoxides are known as catalysts for esterification processes. During the esterification, these compounds are frequently converted to insoluble compounds of titanium which result in a hazy product. The presence of a haze is a particular disadvantage in polyesters which have a high viscosity and/or high melting point and are therefore difficult to filter. Furthermore, many organotitanium compounds which are effective catalysts in the manufacture of polyesters such as polyethylene terephthalate are known to produce unacceptable yellowing in the final polymer.
  • GB-A-2 314 081 relates to an esterification process in which these problems are partially solved but there is still a need for a catalyst system which induces little or no yellowing in a polyester produced using the catalyst. Furthermore, there is a need for a catalyst which produces polyester which is heat stable in the melt.
  • a catalyst composition suitable for use as a catalyst for the preparation of an ester comprises an organometallic compound which is the reaction product of i. an alkoxide or condensed alkoxide of at least one metal selected from titanium, zirconium or aluminium, ii. an alcohol containing at least two hydroxyl groups, iii. a base and iv. an organophosphorus compound of general formula PX(OR 1 ) a (R 2 ) where X is S or
  • R 1 is alkyl/aryl, substituted alkyl/aryl, ether-alkyl, alkoxy, -C(0)R 3 where R 3 is (optionally substituted) C 1-6 alkyl or carboxylic acid (or derivative thereof), -(CH 2 ) x COOR 4 , where R 4 is alkyl, preferably C 1-6 alkyl and x is preferably 1 - 3; each R 2 is independently H, alkyl/aryl, substituted alkyl/aryl, ether-alkyl, e.g.
  • a process for the preparation of an ester comprises carrying out an esterification reaction in the presence of a catalyst composition comprising an organometallic compound which is the reaction product of:- i. an alkoxide or condensed alkoxide of at least one metal selected from titanium, zirconium or aluminium, ii. an alcohol containing at least two hydroxyl groups, iii. a base and iv. an organophosphorus compound of general formula PX(OR 1 ) a (R 2 ) b where X is S or
  • R 1 is alkyl/aryl, substituted alkyl/aryl, ether-alkyl, alkoxy, -C(0)R 3 where R 3 is (optionally substituted) C ⁇ -6 alkyl or carboxylic acid (or derivative thereof), -(CH 2 ) x COOR 4 , where R 4 is alkyl, preferably C 1-6 alkyl and x is preferably 1 - 3; each R 2 is independently H, alkyl/aryl, substituted alkyl/aryl, ether-alkyl, e.g.
  • the organometallic compound suitable for use in an esterification process further comprises a 2-hydroxy carboxylic acid.
  • the organometallic compound comprises the reaction product of an alkoxide (also known as an orthoester) or condensed alkoxide (or orthoester) of at least one metal selected from titanium, zirconium or aluminium. Normally an alkoxide or condensed alkoxide of one of the selected metals is used but it is within the scope of the invention to use an alkoxide or condensed alkoxide of more than one of the selected metals.
  • an alkoxide or condensed alkoxide of one of the selected metals is used but it is within the scope of the invention to use an alkoxide or condensed alkoxide of more than one of the selected metals.
  • a titanium, zirconium or aluminium alkoxide or condensed alkoxide for clarity we refer hereinafter to a titanium, zirconium or aluminium alkoxide or condensed alkoxide, and all such references should be taken to include alkoxides or condensed alkoxides of more
  • the alkoxide has the formula M(OR) or AI(OR) 3 where M is titanium or zirconium and R is an alkyl group. More preferably R contains 1 to 6 carbon atoms and particularly suitable alkoxides include tetraisopropoxy titanium, tetra-n-butoxy titanium, tetra-n-propoxy zirconium, tetra-n-butoxy zirconium and tetra-iso-butoxy aluminium.
  • the condensed alkoxides suitable for preparing the organometallic compounds used in this invention are typically prepared by careful hydrolysis of titanium, zirconium or aluminium alkoxides.
  • Titanium or zirconium condensed alkoxides are frequently represented by the formula RO[M(OR) 2 0] n R in which R represents an alkyl group and M represents titanium or zirconium.
  • n is less than 20 and more preferably is less than 10.
  • R contains 1 to 12 carbon atoms, more preferably, R contains 1 to 6 carbon atoms and useful condensed alkoxides include the compounds known as polybutyl titanate, polyisopropyl titanate and polybutyl zirconate.
  • the alcohol containing at least two hydroxyl groups is a dihydric alcohol and can be a 1 ,2-diol such as 1 ,2-ethanediol or 1 ,2-propanediol, a 1 ,3-diol such as 1 ,3-propanediol, a 1 ,4- diol such as 1,4-butanediol, a diol containing non-terminal hydroxyl groups such as 2-methyl- 2,4-pentanediol or a dihydric alcohol containing a longer chain such as diethylene glycol or a polyethylene glycol.
  • a 1 ,2-diol such as 1 ,2-ethanediol or 1 ,2-propanediol
  • a 1 ,3-diol such as 1 ,3-propanediol
  • a 1 ,4- diol such as 1,4-butanediol
  • Preferred dihydric alcohols include 1 ,2-ethanediol, 1 ,3-propanediol and 1 ,4-butanediol.
  • the organometallic compound can also be prepared from a polyhydric alcohol such as glycerol, trimethylolpropane or pentaerythritol.
  • the organometallic compound is prepared by reacting a dihydric alcohol with an alkoxide or condensed alkoxide in a ratio of from 1 to 32 moles of dihydric alcohol to each mole of titanium, zirconium or aluminium. More preferably, the reaction product contains 2 to 25 moles of dihydric alcohol per mole of titanium, zirconium or aluminium and most preferably 4 to 25 moles dihydric alcohol per.mole of titanium, zirconium or aluminium.
  • X is preferably O.
  • the donor group is preferably S, O, N, OH, NH or SH; particularly preferred are O, OH or NH.
  • R 1 and /or R 2 is alkyl, or alkoxy then they are preferably C 1-6 alkyl or alkoxy, e.g. ethyl, propyl or butyl or ethoxy, propoxy or butoxy.
  • R 1 and /or R 2 are substituted alkyl or alkoxy then they are preferably OH- or NH- substituted C 1-10 alkyl or alkoxy groups, for example hydroxypropyl, hydroxyethyl, hydroxymethyl, hydroxypropoxy or hydroxyethoxy, aminopropyl, aminoethyl, aminomethyl, aminopropoxy or aminoethoxy.
  • R 1 and /or R 2 is ether-alkyl it is preferably polyoxyalkyl, especially polyoxyethyl or polyoxypropyl, i.e. it is preferably derived from a polyethylene glycol or polypropylene glycol moiety. Alternatively it is derived from a simple glycol such as ethylene glycol to form a hydroxy-ether group.
  • R 1 and /or R 2 is -OCOR 3 where R 3 is (optionally substituted) C 1-6 alkyl or carboxylic acid (or derivative thereof), then the phosphorus atom is joined via an ester link to a carboxyl- containing compound.
  • a preferred example of such a compound is a residue of a hydroxy carboxylic acid such that the organophosphorus compound is a phosphorus derivative of a hydroxycarboxylic acid such as lactic, citric, tartaric or malic acids for example.
  • R 4 is preferably C1 - C6 alkyl and x is preferably 1
  • a preferred example of such a compound when R is -(CH2)xCOOR 4 is complaint a phosphonoacetate, for example an ethyl phosphonoacetate when x is 1 and R is ethyl.
  • Preferred organophosphorus compounds include phosphite diesters, phosphate triesters and phosphonate diesters.
  • Examples of preferred compounds include triethylphosphonoacetate (TEPA), and di(polyoxyethyl)hydroxymethylphosphonate which are phosphonate diesters.
  • the amount of organophosphorus compound present in the catalyst composition of the invention is usually in the range 0.1 to 4.0 mole of phosphorus to 1 mole of metal (titanium, zirconium or aluminium), preferably in the range 0.1 to 2.0 mole phosphorus to 1 mole metal and most preferably in the range 0.3 to 1.8 mole phosphorus to 1 mole metal.
  • Suitable inorganic bases include inorganic bases such as sodium hydroxide, potassium hydroxide, lithium hydroxide, magnesium hydroxide, calcium hydroxide and ammonium hydroxide.
  • Preferred organic bases include quaternary ammonium compounds such as tetrabutyl ammonium hydroxide, tetraethyl ammonium hydroxide (TEAH), choline hydroxide (trimethyl(2-hydroxyethyl)ammonium hydroxide) or benzyltrimethyl ammonium hydroxide, or alkanolamines such as monoethanolamine, diethanolamine, triethanolamine and triisopropanolamine.
  • TEAH tetrabutyl ammonium hydroxide
  • choline hydroxide trimethyl(2-hydroxyethyl)ammonium hydroxide
  • benzyltrimethyl ammonium hydroxide or alkanolamines such as monoethanolamine, diethanolamine, triethanolamine and triisopropanolamine.
  • Particularly preferred organic bases include choline hydroxide and TEAH, which have been found to produce polyester having particularly good colour properties when used in the catalysts of the invention.
  • the amount of base used is in the range 0.1 to 4.0 mole base per mole of metal (titanium, zirconium or aluminium).
  • the preferred amount is in the range 0.1 to 2.0 mole base per mole of metal and, frequently, the amount of base present is in the range 0.3 to 1.5 mole base per mole of titanium, zirconium or aluminium.
  • 2-hydroxy carboxylic acids When 2-hydroxy carboxylic acids are used in the catalyst compositions of the invention, preferred acids used include lactic acid, citric acid, malic acid and tartaric acid. Some suitable acids are supplied as hydrates or as aqueous mixtures and can be used in this form.
  • the preferred molar ratio of acid to titanium, zirconium or aluminium in the reaction product is 0.5 to 4 moles per mole of titanium, zirconium or aluminium. More preferably the reaction product contains 1.0 to 3.5 moles of 2-hydroxy acid per mole of titanium, zirconium or aluminium.
  • the organometallic compound can be prepared by mixing the components (alkoxide or condensed alkoxide, alcohol containing at least two hydroxyl groups, organophosphorus compound and base, with removal, if desired, of any by-product, (e.g. isopropyl alcohol when the alkoxide is tetraisopropoxytitanium), at any appropriate stage.
  • any by-product e.g. isopropyl alcohol when the alkoxide is tetraisopropoxytitanium
  • the alkoxide or condensed alkoxide and a dihydric alcohol are mixed and, subsequently, a base is added, followed by the organophosphorus compound.
  • a 2-hydroxy carboxylic acid is also present in the reaction product, this is usually added to the alkoxide or condensed alkoxide before the organophosphorus compound is added.
  • all or part of the 2- hydroxy carboxylic acid can be neutralised with the base and the resulting salt added to the other components of the
  • the catalyst composition of the invention may additionally comprise a compound of germanium, antimony or tin and, in general, any compound can be used including mixtures of compounds of more than one of these metals.
  • the preferred compound of germanium is germanium dioxide.
  • the antimony compound is antimony trioxide or a salt of antimony, for example antimony triacetate.
  • tin compounds are suitable, including salts, such as tin acetate and organotin compounds, such as dialkyl tin oxides, for example, dibutyl tin oxide, dialkyl tin dialkanoates, for example, dibutyl tin dilaurate and alkylstannoic acids, for example butylstannoic acid (C 4 H 9 SnOOH).
  • salts such as tin acetate and organotin compounds
  • dialkyl tin oxides for example, dibutyl tin oxide
  • dialkyl tin dialkanoates for example, dibutyl tin dilaurate
  • alkylstannoic acids for example butylstannoic acid (C 4 H 9 SnOOH).
  • the esterification reaction of the process of the invention can be any reaction by which an ester is produced.
  • the reaction may be (i) a direct esterification in which a carboxylic acid or its anhydride and an alcohol react to form an ester or (ii) a transesterification (alcoholysis) in which a first alcohol reacts with a first ester to produce an ester of the first alcohol and a second alcohol produced by cleavage of the first ester or (iii) a transesterification reaction in which two esters are reacted to form two different esters by exchange of alkoxy radicals.
  • Direct esterification or transesterification can be used in the production of polymeric esters and a preferred process of the invention comprises a polyesterification process.
  • carboxylic acids and anhydrides can be used in direct esterification including saturated and unsaturated monocarboxylic acids and anhydrides of such acids such as stearic acid, isostearic acid, capric acid, caproic acid, palmitic acid, oleic acid, palmitoleic acid, triacontanoic acid, benzoic acid, methyl benzoic acid, salicylic acid and rosin acids such as abietic acid, dicarboxylic acids such as phthalic acid, isophthalic acid, terephthalic acid, sebacic acid, adipic acid, azelaic acid, succinic acid, fumaric acid, maleic acid, naphthalene dicarboxylic acid and pamoic acid and anhydrides of these acids and poly carboxylic acids such as trimellitic acid, citric acid, trimesic acid, pyromellitic acid and anhydrides of these acids.
  • saturated and unsaturated monocarboxylic acids and anhydrides of such acids
  • Alcohols frequently used for direct esterification include aliphatic straight chain and branched monohydric alcohols such as butyl, pentyl, hexyl, octyl and stearyl alcohols, dihydric alcohols such as 1 ,2-ethanediol, 1 ,3-propanediol, 1 ,4-butanediol and 1 ,6-hexanediol and polyhydric alcohols such as glycerol and pentaerythritol.
  • monohydric alcohols such as butyl, pentyl, hexyl, octyl and stearyl alcohols
  • dihydric alcohols such as 1 ,2-ethanediol, 1 ,3-propanediol, 1 ,4-butanediol and 1 ,6-hexanediol
  • polyhydric alcohols such as glycerol and pentaery
  • esters employed in an alcoholysis reaction are generally the lower homologues such as methyl, ethyl and propyl esters since, during the esterification reaction, it is usual to eliminate the displaced alcohol by distillation.
  • These lower homologue esters of the acids suitable for direct esterification are suitable for use in the transesterification process according to the invention.
  • (meth)acrylate esters of longer chain alcohols are produced by alcoholysis of esters such as methyl acrylate, methyl methacrylate, ethyl acrylate and ethyl methacrylate.
  • Typical alcohols used in alcoholysis reactions include butyl, hexyl, n-octyl and 2- ethyl hexyl alcohols and substituted alcohols such as dimethylaminoethanol.
  • the esterification reaction is a transesterification between two esters, generally the esters will be selected so as to produce a volatile product ester which can be removed by distillation.
  • polymeric esters can be produced by processes involving direct esterification or transesterification and a particularly preferred embodiment of the esterification process of the invention is a polyesterification reaction in the presence of the catalyst composition described hereinbefore.
  • a polyesterification reaction polybasic acids or esters of polybasic acids are usually reacted with polyhydric alcohols to produce a polymeric ester.
  • Linear polyesters are often produced from dibasic acids such as those mentioned hereinbefore or esters of said dibasic acids and dihydric alcohols.
  • Preferred polyesterification reactions according to the invention include the reaction of terephthalic acid or dimethyl terephthalate with 1 ,2-ethanediol (ethylene glycol) to produce polyethylene terephthalate or with 1 ,3-propanediol (propylene glycol) to produce polypropylene terephthalate or with 1 ,4- butanediol (butylene glycol) to produce polybutylene terephthalate or reaction of naphthalene dicarboxylic acid or dimethyl naphthalenate with 1 ,2-ethanediol to produce polyethylene naphthalate.
  • acids such as isophthalic acid and other glycols such as 1 ,6-hexanediol and polyhydric alcohols such as glycerol, trimethylolpropane and pentaerythritol are also suitable for preparing polyesters.
  • the esterification reaction of the invention can be carried out using any appropriate, known technique for an esterification reaction.
  • a typical process for the preparation of polyethylene terephthalate comprises two stages. In the first stage terephthalic acid or dimethyl terephthalate is reacted with 1 ,2-ethanediol to form a bishydroxyethylterephthalate prepolymer and the by-product water or methanol is removed. The prepolymer is subsequently heated in a second (polycondensation) stage to remove 1 ,2- ethanediol and form a long chain polymer. Either or both these stages may comprise an esterification process according to this invention.
  • a typical direct esterification reaction is the preparation of bis(2-ethylhexyl) phthalate which is prepared by mixing phthalic anhydride and 2-ethyl hexanol.
  • An initial reaction to form a monoester is fast, but the subsequent conversion of the monoester to diester is carried out by refluxing in the presence of the catalyst composition at a temperature of 180-200°C until all the water has been removed. Subsequently the excess alcohol is removed.
  • the ester, first alcohol and catalyst composition are mixed and, generally, the product alcohol (second alcohol) is removed by distillation, often as an azeotrope with the ester. Frequently it is necessary to fractionate the vapour mixture produced from the alcoholysis in order to ensure that the second alcohol is separated effectively without significant loss of product ester or first alcohol.
  • the conditions under which alcoholysis reactions are carried out depend principally upon the components of the reaction and generally components are heated to the boiling point of the mixture used.
  • a preferred process of the invention is the preparation of polyethylene terephthalate.
  • a typical batch production of polyethylene terephthalate is carried out by charging terephthalic acid and ethylene glycol to a reactor along with catalyst composition, if desired, and heating the contents to 260 - 270°C under a pressure of about 0.3 MPa. Reaction commences as the acid dissolves at about 230°C and water is removed. The product is transferred to a second autoclave reactor and catalyst composition is added, if needed. The reactor is heated to 285 - 310°C under an eventual vacuum of 100 Pa to remove ethylene glycol by-product during the ensuing polycondensation reaction. The molten product ester is discharged from the reactor, cooled and chipped. The chipped polyester may be then subjected to solid state polymerisation, if appropriate.
  • a preferred means of adding the catalyst compositions of this invention to a polyesterification reaction is in the form of a slurry or solution in the glycol being used (e.g. ethylene glycol in the preparation of polyethylene terephthalate). This method of addition is applicable to addition of the catalyst composition to the esterification reaction at the first stage or at the second polycondensation stage.
  • the amount of catalyst used in the esterification process of the invention generally depends upon the total metal content (expressed as amount of Ti, Zr or Al) of the catalyst composition. Usually the amount is from 0.1 to 1200 parts per million (ppm) of metal based on weight of product ester for direct or transesterification reactions. Preferably, the amount is from 1 to 650 ppm of total metal based on weight of product ester. In polyesterification reactions the amount used is generally expressed as a proportion of the weight of product polyester and is usually from 0.1 to 550 ppm expressed as total metal (Ti, Zr or Al) based on product polyester.
  • the amount is from 1 to 250 ppm, more preferably 3 to 100 ppm expressed as total metal based on product polyester.
  • the products of this invention have been shown to be effective catalyst compositions for producing esters and polyesters at an economical rate without leading to haze in the final product and with a reduced amount of yellowing of polyesters in comparison to known catalysts. They have also been shown to be stable against precipitation from polyester products when aqueous base or phosphoric acid is added to such products.
  • EXAMPLE 1 Ethylene glycol (49.6 g, 0.8 moles) was added from a dropping funnel to stirred titanium n-butoxide (34 g, 0.1 mole) in a 250 ml flask fitted with stirrer, condenser and thermometer. An aqueous solution of sodium hydroxide, containing 32% NaOH by weight, (6.25 g, 0.05 mole) was added to the reaction flask slowly with mixing to yield a clear yellow liquid. To this liquid was added a di (polyoxoethylene) hydroxymethyl phosphonate available under the trade name Victastab HMP from Akzo Nobel, (18.93 g, 0.052 mole of phosphorus). After removing n-butanol at 70°C under vacuum to constant weight the product was a liquid with a Ti content of 2.76% by weight.
  • EXAMPLE 2 Ethylene glycol (49.6 g, 0.8 moles) was added from a dropping funnel to stirred titanium n-butoxide (34 g, 0.1 mole) in a 250 ml flask fitted with stirrer, condenser and thermometer. An aqueous solution of sodium hydroxide, containing 32% NaOH by weight, (6.25 g, 0.05 mole) was added to the reaction flask slowly with mixing to yield a clear yellow liquid. To this liquid was added an oligomeric phosphonate available under the trade name Fyrol 51 from Akzo Nobel, (7.852 g, 0.052 mole of phosphorus). After removing n-butanol at 70°C under vacuum to constant weight the product was a liquid with a Ti content of 6.64% by weight.
  • Ethylene glycol (49.6 g, 0.8 moles) was added from a dropping funnel to stirred titanium n-butoxide (34 g, 0.1 mole) in a 250 ml flask fitted with stirrer, condenser and thermometer.
  • diethyl-N,N,-bis(2-hydroxyethyl)aminomethyl phosphonate available under the trade name Fyrol 6 from Akzo Nobel, (18.93 g, 0.074 mole of phosphorus). After removing n-butanol at 70°C under vacuum to constant weight the product was a liquid with a Ti content of 7.00% by weight.
  • Ethylene glycol (49.6 g, 0.8 moles) was added from a dropping funnel to stirred titanium n-butoxide (34 g, 0.1 mole) in a 250 ml flask fitted with stirrer, condenser and thermometer.
  • a triethylphosphonoacetate available under the trade name TEPA from Rhodia, (11.7 g, 0.052 mole of phosphorus). After removing n-butanol at 70°C under vacuum to constant weight the product was a liquid with a Ti content of 6.80% by weight.
  • Ethylene glycol (99.2 g, 1.6 moles) was added from a dropping funnel to stirred titanium n- butoxide (34 g, 0.1 mole) in a 250 ml flask fitted with stirrer, condenser and thermometer.
  • a dibutyl hydrogen phosphite available under the trade name DBHP from Rhodia, (10.1g, 0.052 mole of phosphorus). After removing n-butanol at 70°C under vacuum to constant weight the product was a liquid with a Ti content of 6.31% by weight.
  • EXAMPLE 7 (Comparative) Ethylene glycol (496.0 g, 8.00 moles) was added from a dropping funnel to stirred titanium n- butoxide (340 g, 1.00 mole) in a 1 litre fishbowl flask fitted with stirrer, condenser and thermometer. An aqueous solution of sodium hydroxide, containing 32% NaOH by weight, (125 g, 1.00 mole) was added to the reaction flask slowly with mixing to yield a clear pale yellow liquid. To this liquid was then added a butyl acid phosphate, (91.0 g, 0.50 mole of phosphorus) and the resulting mixture was stirred for 1 hour to produce a pale yellow liquid with a Ti content of 4.56% by weight.
  • Ethylene glycol (136 g, 2.2 moles) was added from a dropping funnel to stirred titanium n- butoxide (34 g, 0.1 mole) in a 250 ml flask fitted with stirrer, condenser and thermometer.
  • TEAH tetraethyl ammonium hydroxide
  • Ethylene glycol (136 g, 2.2 moles) was added from a dropping funnel to stirred titanium n- butoxide (34 g, 0.1 mole) in a 250 ml flask fitted with stirrer, condenser and thermometer.
  • ChOH choline hydroxide
  • a polycondensation reaction was carried out in a mechanically-stirred 300 ml glass vessel fitted with side arm and cold trap for collection of monoethyleneglycol.
  • a thermostatically controlled ceramic heating element was used to provide heat and an oil vacuum pump was connected to the cold trap.
  • a nitrogen blanket was provided via a connection to the cold trap.
  • Polyethylene terephthalate was prepared from pure bis(hydroxyethyl)- terephthalate polymer precursor. 100 g of bis(hydroxyethyl)terephtha!ate polymer precursor was placed in the reaction flask under a nitrogen flow, followed by a dilute solution of catalyst component in monoethyleneglycol. For the catalyst (Table 1) the level was set at 30ppm (based on metal content).
  • the catalysts were used to prepare polyethylene terephthalate (PET).
  • Ethylene glycol (2.04 kg) and terephthalic acid (4.55 kg) were charged to a stirred, jacketed reactor.
  • the catalyst and other additives were added and the reactor heated to 226 - 252 °C at a pressure of 40 psi to initiate the first stage direct esterification (DE) process. Water was removed as it was formed with recirculation of the ethylene glycol.
  • DE reaction direct esterification
  • the stabilisers were added and the mixture heated to 290 ⁇ 2 °C. under vacuum to remove ethylene glycol and yield polyethylene terephthalate.
  • the final polyester was discharged once a constant torque had been reached which indicated an IV of around 0.62.
  • the polymer was analysed and the results are shown in Table 2. Polymer Analysis
  • the colour of the polymer was measured using a Byk-Gardner Colourview spectrophotometer.
  • Cielab L*, a* and b* scale where the b- value describes yellowness.
  • the yellowness of the polymer increases with b-value.
  • the polymer intrinsic viscosities were measured by glass capNlary viscometry using 60/40 phenol/1, 1, 2, 2-tetrachlorethane as solvent. The results are shown in Tables 1 - 2.
  • Discharge of molten polymer from a reactor takes place over a period of time during which the polymer is held in the molten phase at elevated temperature.
  • the time of discharge of the polymer was noted and is shown in the tables.
  • TIPT tetraisopropoxy titanium Phosphorus compound added was HordaphosTM MEG phosphate solution from Clariant AG at the beginning of the DE reaction Phosphorus compound added was HordaphosTMDGB(LP) from Clariant AG at the beginning of the PC reaction

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

L'invention concerne une composition catalytique conçue pour une utilisation comme un catalyseur pour la préparation d'un ester. Ladite composition comprend un composé organométallique qui est le produit de réaction d'un alcoxyde ou d'un alcoxyde condensé d'au moins un métal sélectionné de titane, zirconium ou aluminium ; un alcool contenant au moins deux groupes hydroxy ; une base, et un composé organophosphoré de formule PX(OR1)a(R2)b, dans laquelle X représente S ou O, R1 représente alkyle/aryle, alkyle/aryle substitué, éther-alkyle, alcoxy, -COR3, R3 représentant alkyle C1-6 (éventuellement substitué) ou acide carboxylique ( ou ses dérivés), -(CH2)xCOOR4, R4 représentant alkyle de préférence alkyle C1-6 et x représentant de préférence 1 3 ; chaque R2 représente de manière indépendante H, alkyle/aryle, alkyle/aryle éventuellement substitué, par exemple polyoxyalkyle, en particulier polyoxyéthyle ou polyoxypropyle, alcoxy, -OCOR3, R3 représentant alkyle C1-6 éventuellement substitué ou acide carboxylique (ou ses dérivés), -(CH2)xCOOR4, R4 représentant alkyle, de préférence alkyle C1-6 et x représentant de préférence 1 3. Au moins un R1 ou R2 contient un groupe de donneurs capable de coordonner ou de former un lien covalent avec le métal, a est de l'ordre de 1 à 3, b est de l'ordre de 0 à 2 et a+b=3.
PCT/GB2002/005281 2001-11-26 2002-11-26 Catalyseur et procede de preparation d'un ester WO2003045550A1 (fr)

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005097321A1 (fr) * 2004-03-26 2005-10-20 E.I. Dupont De Nemours And Company Catalyseur d'esterification et procede connexe
CN1300246C (zh) * 2003-12-19 2007-02-14 上海交通大学 原位生成纳米二氧化钛制备抗紫外聚酯的方法
CN103539926A (zh) * 2012-07-12 2014-01-29 中国石油化工股份有限公司 钛系聚酯的生产方法
CN110090667A (zh) * 2018-01-30 2019-08-06 南京大学昆山创新研究院 锆金属有机骨架UiO-66催化剂的制备方法及其应用
CN110183629A (zh) * 2019-05-21 2019-08-30 中国石油化工股份有限公司 一种耐水解聚酯用组合物及组合物溶液的制备方法及应用
CN110252266A (zh) * 2016-11-14 2019-09-20 广西民族大学 一种酯化修饰的松香基高分子微球及其制备的色谱柱

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999028033A1 (fr) * 1997-12-02 1999-06-10 Acma Limited Catalyseurs d'esterification
EP1156070A1 (fr) * 2000-05-17 2001-11-21 SK Chemical Co., Ltd. Méthode de préparation d'une résine polyester copolymérisée avec du 1,4-cyclohexanediméthanol

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999028033A1 (fr) * 1997-12-02 1999-06-10 Acma Limited Catalyseurs d'esterification
EP1156070A1 (fr) * 2000-05-17 2001-11-21 SK Chemical Co., Ltd. Méthode de préparation d'une résine polyester copolymérisée avec du 1,4-cyclohexanediméthanol

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1300246C (zh) * 2003-12-19 2007-02-14 上海交通大学 原位生成纳米二氧化钛制备抗紫外聚酯的方法
WO2005097321A1 (fr) * 2004-03-26 2005-10-20 E.I. Dupont De Nemours And Company Catalyseur d'esterification et procede connexe
CN103539926A (zh) * 2012-07-12 2014-01-29 中国石油化工股份有限公司 钛系聚酯的生产方法
CN103539926B (zh) * 2012-07-12 2015-11-18 中国石油化工股份有限公司 钛系聚酯的生产方法
CN110252266A (zh) * 2016-11-14 2019-09-20 广西民族大学 一种酯化修饰的松香基高分子微球及其制备的色谱柱
CN110252266B (zh) * 2016-11-14 2022-09-23 广西民族大学 一种酯化修饰的松香基高分子微球及其制备的色谱柱
CN110090667A (zh) * 2018-01-30 2019-08-06 南京大学昆山创新研究院 锆金属有机骨架UiO-66催化剂的制备方法及其应用
CN110183629A (zh) * 2019-05-21 2019-08-30 中国石油化工股份有限公司 一种耐水解聚酯用组合物及组合物溶液的制备方法及应用
CN110183629B (zh) * 2019-05-21 2021-09-07 中国石油化工股份有限公司 一种耐水解聚酯用组合物及组合物溶液的制备方法及应用

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