WO2007003966A1 - Novel zirconium compound, catalyst and its use for polyurethane manufacture - Google Patents

Novel zirconium compound, catalyst and its use for polyurethane manufacture Download PDF

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Publication number
WO2007003966A1
WO2007003966A1 PCT/GB2006/050187 GB2006050187W WO2007003966A1 WO 2007003966 A1 WO2007003966 A1 WO 2007003966A1 GB 2006050187 W GB2006050187 W GB 2006050187W WO 2007003966 A1 WO2007003966 A1 WO 2007003966A1
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Prior art keywords
deaa
catalyst
compound
alkyl
derived
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PCT/GB2006/050187
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French (fr)
Inventor
Bruno Frederic Stengel
Arran Tulloch
Swagata Nanda
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Johnson Matthey Plc
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Publication date
Application filed by Johnson Matthey Plc filed Critical Johnson Matthey Plc
Priority to KR1020087002730A priority Critical patent/KR101319112B1/en
Priority to AU2006264653A priority patent/AU2006264653B2/en
Priority to JP2008520010A priority patent/JP5436855B2/en
Priority to US11/994,704 priority patent/US8586696B2/en
Priority to EP06744367.1A priority patent/EP1899061B1/en
Priority to CN2006800281649A priority patent/CN101232943B/en
Priority to CA2613743A priority patent/CA2613743C/en
Priority to BRPI0612399-6A priority patent/BRPI0612399A2/en
Publication of WO2007003966A1 publication Critical patent/WO2007003966A1/en

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/16—Catalysts
    • C08G18/22—Catalysts containing metal compounds
    • C08G18/222—Catalysts containing metal compounds metal compounds not provided for in groups C08G18/225 - C08G18/26
    • 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
    • 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
    • B01J21/00—Catalysts comprising the elements, oxides, or hydroxides of magnesium, boron, aluminium, carbon, silicon, titanium, zirconium, or hafnium
    • B01J21/06—Silicon, titanium, zirconium or hafnium; Oxides or hydroxides 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
    • B01J31/16—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
    • B01J31/1805—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 nitrogen
    • 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
    • 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
    • B01J31/2234—Beta-dicarbonyl ligands, e.g. acetylacetonates
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/16—Catalysts
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08—Processes
    • C08G18/16—Catalysts
    • C08G18/22—Catalysts containing metal compounds
    • 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
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30—Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/34—Other additions, e.g. Monsanto-type carbonylations, addition to 1,2-C=X or 1,2-C-X triplebonds, additions to 1,4-C=C-C=X or 1,4-C=-C-X triple bonds with X, e.g. O, S, NH/N
    • B01J2231/341—1,2-additions, e.g. aldol or Knoevenagel condensations
    • 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
    • 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
    • C08G2110/00—Foam properties
    • C08G2110/0025—Foam properties rigid

Definitions

  • the present invention concerns a novel catalyst comprising a zirconium chelate, and its use to catalyse the reaction of an isocyanate-containing compound with an alcohol or an amine to form a polyurethane or a polyurea.
  • Polyurethanes are typically made by reacting a polyisocyanate compound with a polyol in the presence of an organometallic catalyst.
  • Catalysts for polyurethane manufacture are conventionally based on tin compounds such as dibutyl tin dilaurate or compositions of mercury such as phenyl mercuric neodecanoate. More recently, compounds based upon metals such as titanium or nickel have been used.
  • Such compounds are of general formula RO-M(L 1 ) X (L 2 ) y (L 3 ) z where R is alkyl or a hydroxy-alkyl, hydroxyalkoxyalkyl, or (hydroxy)polyoxyalkyl group and up to 2 of L 1 to L 3 may represent an amide of acetoacetic acid.
  • R is alkyl or a hydroxy-alkyl, hydroxyalkoxyalkyl, or (hydroxy)polyoxyalkyl group and up to 2 of L 1 to L 3 may represent an amide of acetoacetic acid.
  • These compounds have a single labile -OR ligand and were believed to function as a cure catalyst by exchange or insertion of the polyol or of the isocyanate at the labile site on the organometallic composition, by displacement of the OR group.
  • US-A-5846897 discloses zirconium compounds with diketones or alkylacetoacetates which catalyse the isocyanate - alcohol reaction having the chemical structure: Me (X1 , X2, X3, X4) wherein Me is zirconium (Zr) or hafnium (Hf) and X1 , X2, X3, and X4, are the same or different and selected from the group consisting of a diketone and an alkylacetoacetate having the structures: RICOCH 2 COR 2 and RIOCOCH 2 COR 2 wherein each of R 1 and R 2 is a branched or linear C1 -C20 hydrocarbon and at least one of X1 , X2, X3, and X4 is a diketone with structure (II) wherein the total number of carbons in R 1 + R 2 is at least 4.
  • Patil et al J. Mater Chem 2003, 13, 2177 - 2184 have used zirconium bis(isopropoxide)bis(N,N- diethylacetoacetamide) as a precursor for the metal-organic chemical vapour deposition of zirconium dioxide.
  • the catalyst is of formula Zr(L)(A 1 )(A 2 )(A 3 ) where L represents a ketoamide ligand, A 1 , A 2 & A 3 may be the same or different and each represent a ligand derived from a compound selected from the group consisting of:- an alcohol, a polyol, an alkyl acetoacetate, a diketone, a ketoamide, a carboxylic acid or ester thereof, an alkanolamine, a phosphoric acid ester and a sulphonic acid or ester thereof; provided that either: (i) none of A 1 , A 2 & A 3 represent a ligand -OR where R is alkyl or a hydroxy-alkyl, hydroxyalkoxyalkyl, or (hydroxy)polyoxyalkyl group, or
  • a 1 , A 2 & A 3 represent a ligand -OR where R is alkyl or a hydroxy- alkyl, hydroxyalkoxyalkyl, or (hydroxy)polyoxyalkyl group.
  • R is alkyl or a hydroxy- alkyl, hydroxyalkoxyalkyl, or (hydroxy)polyoxyalkyl group.
  • a ligand derived from a compound in the sense that the ligand has been formed by the reaction of the compound with a zirconium compound to form the claimed catalyst or a precursor thereto.
  • a ligand derived from an alcohol ROH is present in the catalyst as an alkoxide RO-
  • a ligand derived from a carboxylic acid RCOOH is present in the catalyst as a carboxylate RCOO-.
  • ligand L or A the compounds referred to as forming a ligand L or A will be present in the catalyst in their reacted form and generally not in the unreacted form of the compound. Most of the ligand-forming compounds herein react with a zirconium compound though a reactive -OH to form an -0-Zr- linkage in the catalyst.
  • the ketoamide ligand, L is derived from a ketoamide of general structure shown in Formula 1 , which is believed to react with the zirconium alkoxide or haloalkoxide through its "enol" form, shown in Formula 1', to form a ligand R 1 R 2 COCR 3 CR 4 O-.
  • R 1 , R 2 and R 4 are independently selected from H, linear or branched alkyl or aryl.
  • R 1 , R 2 and/or R 4 are alkyl groups, they preferably contain from 1 to 22 carbon atoms, more preferably from 1 to 8 C atoms.
  • R 1 , R 2 and/or R 4 are aryl groups, they may be unsubstituted or substituted with alkyl, halogen or ether groups.
  • aryl we include polycyclic aromatic groups. It is preferred that R 1 , R 2 and/or R 4 are not H, and tertiary amides, i.e. where neither R 1 nor R 2 is H are preferred.
  • R 3 is selected from H or linear or branched alkyl, preferably containing from 1 to 22 carbon atoms, more preferably from 1 to 8 C atoms.
  • L is preferably a ligand derived from a N,N-dialkyl acetoacetamide (DAAA) and a preferred dialkyl acetoacetamide comprises N,N-diethylacetoacetamide (DEAA).
  • DAAA N,N-dialkyl acetoacetamide
  • DEAA N,N-diethylacetoacetamide
  • Other suitable ketoamides include acetoacetanilide, o-acetoacetaniside, 2'-benzoylacetanilide, 4'- chloroacetoacetanilide, p-acetoacetaniside, N,N-dimethylacetoacetamide,
  • the reaction product may contain more than 1 mole of ketoamide per mole of zirconium when at least one of A 1 , A 2 & A 3 is derived from a ketoamide.
  • the product may contain up to four moles of ketoamide bound to the zirconium atom to form a chelate.
  • Each ketoamide ligand may be the same as or different from each other ketoamide ligand.
  • each ketoamide ligand is derived from the same ketoamide compound.
  • the product may also contain a free ketoamide compound, i.e. there may be more than 4 moles of ketoamide per mole of zirconium.
  • the catalyst is a composition comprising from 1 to 10 moles, more preferably from 2 to 4 moles, of free ketoamide per mole of zirconium.
  • One preferred such embodiment comprises a composition of formula [Zr(DEAA) 4 + 2DEAA].
  • Zr(DEAA)X this means that the zirconium compound has x ligands derived from DEAA, which is present in the catalyst in its reacted form.
  • a 1 , A 2 & A 3 may be the same or different and each represent a ligand derived from a compound selected from the group consisting of an alcohol, a polyol, an alkyl acetoacetate, a diketone, a ketoamide, a carboxylic acid or ester thereof, an alkanolamine or a phosphoric acid ester.
  • the alcohol is of general formula R-OH where R is an alkyl or aryl (including polyaryl) group. Where R is aryl, we include phenol, napthol and substituted versions of these, e.g. alkylphenols such as dodecylphenol.
  • R is alkyl, more preferably an alkyl group containing from 1 to 12 C atoms, and most preferably an alkyl group containing from 2 to 8 C atoms.
  • each R may or may not be the same as the other(s).
  • Preferred alcohols include, ethanol, isopropanol, n-propanol, tertiary butanol, n- butanol, 2-ethylhexanol, amyl alcohol, tert-amyl alcohol, hexanol, cyclohexanol, phenol, dodecylphenol and naphthol.
  • the alcohol reacts with a zirconium compound to form an alkoxide or aryloxide RO- ligand.
  • a zirconium compound to form an alkoxide or aryloxide RO- ligand.
  • the catalyst has the general formula Zr(ketoamide) 2 (OR) 2 where R is alkyl, more preferably an alkyl group containing from 1 to 12 C atoms, and most preferably an alkyl group containing from 2 to 8 C atoms.
  • the polyol may be a monomeric alcohol having more than one hydroxy group, for example ethylene glycol, 1 ,3-propylene glycol, 1 ,4-butane diol, or a dimeric or polymeric alcohol such as diethylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol.
  • the polyol also includes polyester polyols and polyether polyols of the type typically used in the manufacture of poyurethanes and which are commercially available. Hydroxy- functionalised resins may also be suitable for forming one or more of the A ligands in general formula 1. Such resins include hydroxyl-containing resins which are sold for use in printing inks, preferably having a hydroxyl number of from about 100 to about 500, especially from about 200 to about 400 mg KOH/g (tested according to DIN 53 240).
  • Suitable synthetic resins include ketone- aldehyde resins especially ketone-formaldehyde resins such as hydrogenated acetophenone formaldehyde condensation resins, cyclohexanone-formaldehyde condensation resins and urethane-modified ketone aldehyde resins.
  • ketone- aldehyde resins especially ketone-formaldehyde resins such as hydrogenated acetophenone formaldehyde condensation resins, cyclohexanone-formaldehyde condensation resins and urethane-modified ketone aldehyde resins.
  • Such resins are available from Degussa AG as Synthetic Resins 1201 , CA and SK, for example.
  • each molecule may bond multiply to the same zirconium atom or alternatively it may bond to more than one zirconium atom to form a bridge between the zirconium atoms. It is likely that in such compounds there is a mixture containing bridged and non-bridged structures.
  • the catalyst is of general formula Zr(ketoamide) 2 (polyol) and/or Zr 2 (ketoamide) 4 (polyol) 2 and/or higher oligomeric bridged structures where (polyol) is in each case a ligand derived from the polyol by reaction of two hydroxy functions with zirconium to form two alkoxide bonds.
  • Zr(L) (A)(polyol) compound therefore refer to the empirical formula and include compounds in which bridged dimeric and oligomeric forms are present.
  • Preferred examples of this type include Zr(DEAA) 2 (1 ,3-propanedioxide), Zr(DEAA) 2 (1 ,4-butanedioxide) and Zr(DEAA) 2 (diethyleneglycoxide).
  • a 1 , A 2 and/or A 3 may each represent a ligand derived from an alkyl acetoacetate, i.e. an ester of an alkyl alcohol R 5 OH with acetoacetic acid wherein R 5 is a branched or linear C1 -C20 hydrocarbon; more preferably R 5 contains from 1 to 8 carbon atoms.
  • Ethylacetoacetate (EAA) is a particularly preferred alkyl acetoacetate compound.
  • Zr(EAA)n we mean a zirconium compound having n ligands derived from ethylacetoacetate.
  • a 1 , A 2 and/or A 3 may each represent a ligand derived from a diketone which is preferably a ⁇ - diketone of general formula R 6 COCH 2 COR 7 wherein each of R 6 and R 7 is a branched or linear C1 -C20 hydrocarbon.
  • Preferred diketones include acetylacetone (2,4-pentanedione), 2,4- heptanedione and alkyl-substituted versions thereof and 3,5-heptanedione and alkyl-substituted versions thereof.
  • a 1 , A 2 and/or A 3 may each represent a ligand derived from a carboxylic acid or ester thereof.
  • Suitable carboxylic acids include benzoic acid and alkyl carboxylic acids, for example a C 2 - C 30 carboxylic acid, especially a C 4 - C 22 carboxylic acid such as butyric, neodecanoic, stearic, isostearic, oleic or 2-ethyl-hexylcarboxylic acid.
  • the carboxylic acid or ester may contain more than one carboxylic acid group such as malonic acid, tartaric acid and their esters, especially alkyl esters e.g. diethyl malonate.
  • Hydroxycarboxylic acids such as lactic acid, citric acid, oxalic acid may also form suitable ligands with zirconium.
  • a 1 , A 2 and/or A 3 may each represent a ligand derived from an alkanolamine, i.e. a compound of general formula HO(CH 2 ) X NR 8 2 where R 8 comprises HO(CH 2 )X or an alkyl group or hydrogen.
  • X is an integer and preferably ranges from 1 to 8.
  • Preferred alkanolamines include ethanolamine, diethanolamine and triethanolamine although others are suitable.
  • a 1 , A 2 and/or A 3 may each represent a ligand derived from an organophosphorus compound having a P-OH group, particularly a phosphate ester, i.e. an alkyl or aryl acid phosphate, or a salt thereof comprising a dialkyl phosphate, a diaryl phosphate, a monoalkyl phosphate, a monoaryl phosphate or a mixture of two or more of a dialkyl phosphate, a diaryl phosphate, a monoalkyl phosphate and a mono aryl phosphate, a phosphonate ester or a salt thereof comprising an alkyl or aryl phosphonate or salts thereof, an alkyl or aryl pyrophosphate, an alkyl or aryl phosphonic acid or alkyl or aryl ester thereof or a salt thereof, a dialkyl or aryl phosphinic acid or salt thereof.
  • a phosphate ester
  • the organophosphorus compound contains a P-OH group, i.e. an acidic group or its salt, i.e. a P-O " M + group where M is metal or ammonium.
  • Preferred organophosphorus compounds comprise an alkyl phosphate compound which may be a mono- or a di-alkyl phosphate or is conveniently a mixture of mono- and dialkyl phosphates, such mixtures being more readily available than pure mono- or a di-alkyl phosphates.
  • Monoalkyl phosphates generally have a formula (R 9 O)PO(OH) 2 .
  • Dialkyl phosphates generally have the formula (R 9 O)(R 10 O)PO(OH).
  • R 9 , R 10 may be the same or different and represent a linear or branched alkyl group usually containing up to 8 carbon atoms and preferably containing up to 5 carbon atoms. Usually, but not necessarily, R 9 ,and R 10 are identical. Preferably R 9 , and R 10 are selected from n-butyl, sec-butyl, ferf-butyl, /so-propyl, n-propyl, ethyl, methyl, phenyl, amyl and ethyl-hexyl.
  • Suitable phosphonate ester, phosphonic acid, phosphinic acid or salt thereof comprises an alkyl or aryl phosphonate, phosphonic acid or their salts and generally have a formula
  • R 11 and R 12 each represent a hydrogen atom or an aryl group or an alkyl group containing up to 8 carbon atoms and preferably containing up to 5 carbon atoms and n is 1 or 2.
  • a 1 , A 2 and/or A 3 may each represent a ligand derived from a sulphonic acid or ester thereof, i.e. a compound of general formula R 13 SO 3 H or its ester where R is aryl or alkyl.
  • suitable sulphonic acids include methane sulphonic acid and substituted benzene sulphonic acids such as dodecylbenzene sulphonic acid. Salts of these sulphonic acids are also suitable, for example alkali metal salts such as the sodium salt and quaternary ammonium salts.
  • the catalyst of the invention preferably comprises the reaction product of a zirconium alkoxide or haloalkoxide with a ketoamide compound and optionally with at least one other ligand- forming compound.
  • the compounds of the invention may be made by reacting a zirconium compound such as an alkoxide, a halide or haloalkoxide with the ketoamide and then with the other compound(s) to form the A ligands if necessary. Where the A-ligands are alkoxide, these may form part of the starting zirconium compound.
  • Zirconium haloalkoxides may be represented by the formula Zr(OR) x .
  • the haloalkoxides may be of mixed formulation and therefore x need not be an integer.
  • the preferred halides are chloride and bromide, particularly chloride.
  • the zirconium alkoxide or haloalkoxide is a zirconium alkoxide of formula Zr(OR) 4 , where R has the meaning described above. Each R may or may not be the same as each other R.
  • the zirconium alkoxide is a tetra-alkyl alkoxide where all alkoxide groups are the same.
  • Preferred zirconium alkoxides include tetra-i-propoxy zirconium, tetra- ethyl zirconium, tetra-n-propoxy zirconium and tetra-n-butoxy zirconium since these are readily available commercial materials.
  • the zirconium alkoxide is a mixed alkoxide.
  • This embodiment is particularly useful where one or more of the OR groups is derived from an alkoxide which is less readily available.
  • Suitable zirconium alkoxides may therefore comprise Zr(isopropoxide) 2 (2-ethylhexoxide) 2 , Zr(n- butoxide) 2 (2-ethylhexoxide) 2 , Zr(n-butoxide) 2 (tert-amylalkoxide) 2 , Zr(isopropoxide) 2 (tert- amylalkoxide) 2 .
  • the catalyst composition may additionally comprise a solvent or diluent.
  • the solvent or diluent may be a compound that coordinates with the zirconium catalyst or it may be non-coordinating.
  • the solvent may comprise an alcohol (which may be alcohol liberated in the reaction of a zirconium alkoxide with the ketoamide).
  • Suitable solvents include polyols (e.g.
  • a similar polyol to that used in a polyurethane reaction for which the compound is used as catalyst such as 1 ,4-butane diol, 1 ,3-propylene glycol, ethylene glycol, diethylene glycol, a polyethylene glycol, a polypropylene glycol, a polyester polyol, a ketoamide, particularly the ketoamide used to form the catalyst, ethylacetoacetate, acetylacetone, diethylmalonate or an excess of a compound used to form one of the A ligands.
  • Examples of preferred catalysts comprise compounds of the following formulae:- Zr(DEAA) 2 (2- ethylhexoxide) 2 , Zr(n-butoxide) 2 (DEAA) 2 , Zr(n-propoxide) 2 (DEAA) 2 , Zr(DEAA) 2 (tert- amylalkoxide) 2, Zr(isopropoxide) 2 (DEAA) 2 , Zr(DEAA) 4 , Zr(t-butoxide) 2 (DEAA) 2 , Zr(DEAA) 4 ,
  • These catalysts may also include additional quantities of at least one of the ligand-forming compounds which are assumed to be present in a non-complexed state. In particular free
  • DEAA ethylacetoacetate, acetylacetone or polyol, especially diethylene glycol has been found to be of benefit.
  • the catalyst does not comprise a compound of bismuth as a co- catalyst.
  • the catalyst composition is useful in the manufacture of polyurethanes, i.e. as a cure catalyst for the reaction of a polyisocyanate with a compound containing an active hydrogen, especially a hydroxyl group, in particular a a polyol; or an amino compound.
  • Applications of such polyurethanes are very diverse and include mouldings, foams, adhesives, coatings, cast or spray elastomers, casting resins etc.
  • the catalyst composition may also be used to catalyse the reaction of a polyisocyanate binder with hydrous materials such as those derived from wood or plant fibres, e.g. as used in the manufacture of composite boards for the construction industry.
  • Organic polyisocyanate compound or mixture of organic polyisocyanate compounds may be suitable provided said compounds have at least 2 isocyanate groups.
  • Organic polyisocyanates include diisocyanates, particularly aromatic diisocyanates, and isocyanates of higher functionality.
  • organic polyisocyanates include aliphatic isocyanates such as hexamethylene diisocyanate; and aromatic isocyanates such as m- and p-phenylene diisocyanate, tolylene-2,4- and tolylene- 2,6-diisocyanate, diphenylmethane-4,4'-diisocyanate, chlorophenylene- 2,4-diisocyanate, naphthylene-1 ,5-diisocyanate, diphenylene-4,4'- diisocyanate, 4,4'-diisocyanate-3,3'-dimethyl-diphenyl, 3-methyldiphenylmethane-4,4'-di- isocyanate and diphenyl ether diisocyanate; and cycloaliphatic diisocyanates such as cyclohexane-2,4- and -2,3-diisocyanate, 1-methylcyclohexyl-2,4- and -2,
  • Modified polyisocyanates containing isocyanurate, carbodiimide or uretonimine groups may be used and are generally chosen when particular physical properties are desired.
  • Blocked polyisocyanates like the reaction product of a phenol or an oxime and a polyisocyanate, may be used, where they have a deblocking temperature below the temperature applied in use.
  • the organic polyisocyanate may also be an isocyanate-ended prepolymer made by reacting an excess of a diisocyanate or higher functionality polyisocyanate with a polyol such as, for example a polyether polyol or a polyester polyol.
  • Water-emulsifiable organic polyisocyanates like those described in UK patent no. 1 444 933, in European patent publication no. 516 361 and in PCT patent publication no. 91/03082 can also be used.
  • isocyanates may be used, for example a mixture of tolylene diisocyanate isomers such as the commercially available mixtures of 2,4- and 2,6-isomers and also the mixture of di- and higher polyisocyanates.
  • Mixtures of diisocyanates known commercially as "crude MDI" contain about 60% of 4,4'-diphenylmethane diisocyanate along with other isomeric and analogous higher polyisocyanates.
  • Polyisocyanate mixtures may optionally contain monofunctional isocyanates such as p-ethyl phenylisocyanate.
  • Such mixtures are well-known in the art and include the crude phosgenation products containing methylene bridged polyphenyl polyisocyanates, including diisocyanate, triisocyanate and higher polyisocyanates together with any phosgenation by-products.
  • Preferred isocyanates are those wherein the isocyanate is an aromatic diisocyanate or polyisocyanate of higher functionality such as a pure diphenylmethane diisocyanate or a mixture of methylene bridged polyphenyl polyisocyanates containing diisocyanates, tri isocyanates and higher functionality polyisocyanates.
  • Methylene bridged polyphenyl polyisocyanates are well known in the art. They are prepared by phosgenation of corresponding mixtures of polyamines. For convenience, polymeric mixtures of methylene bridged polyphenyl polyisocyanates containing diisocyanate, triisocyanate and higher functionality polyisocyanates are referred to hereinafter as polymeric MDI.
  • Polyisocyanates suitable for use with the organometallic complexes of the invention include SUPRASECTM DNR, SUPRASECTM 2185, RUBINATETM M and RUBINATETM 1840, all available from Huntsman Polyurethanes.
  • the polyisocyanate is liquid at room temperature.
  • Suitable polyisocyanates are well known in the art.
  • the polyol component may be any suitable for the manufacture of polyurethanes and includes polyester-polyols, polyester-amide polyols, polyether-polyols, polythioetherpolyols, polycarbonate polyols, polyacetal polyols, polyolefin polyols polysiloxane polyols, dispersions or solutions of addition or condensation polymers in polyols of the types described above, often referred to as "polymer" polyols.
  • polyester-polyols polyester-amide polyols
  • polyether-polyols polythioetherpolyols
  • polycarbonate polyols polyacetal polyols
  • polyolefin polyols polysiloxane polyols dispersions or solutions of addition or condensation polymers in polyols of the types described above, often referred to as "polymer" polyols.
  • a mixture of polyols is used to manufacture polyurethane having particular physical properties.
  • the polyol or polyols is selected to have a molecular weight, backbone type and hydroxy functionality which is tailored to the requirements of the formulator.
  • the polyol includes a chain extender, which is often a relatively short-chain diol such as 1 ,4-butane diol or diethylene glycol or a low molecular weight polyethylene glycol.
  • chain extender in commercial use, such as diamines, e.g. MOCA (4,4-methylene bis (2-chloroaniline)) may also be used.
  • Suitable polyols include the polyalkylene ether- and polyester-polyols.
  • the polyalkylene ether polyols include the poly(alkylene oxide) polymers such as poly( ethylene oxide) and poly(propylene oxide) polymers and copolymers with terminal hydroxyl groups derived from polyhydric compounds, including diols and triols; for example, among others, ethylene glycol, propylene glycol, 1 ,3-butane diol, 1 ,4-butane diol, 1 ,6-hexane diol, neopentyl glycol, diethylene glycol, dipropylene glycol, pentaerythritol, glycerol, diglycerol, trimethylol propane and like low molecular weight polyols.
  • High molecular weight polyether polyol may be used. Also, mixtures of high molecular weight polyether polyols such as mixtures of di- and tri-functional materials optionally with lower molecular weight or different chemical composition materials may be used.
  • Useful polyester polyols include polylactones, e.g.
  • polycaprolactone and those produced by reacting a dicarboxylic acid (which may be an aliphatic or aromatic dicarboxylic acid or anhydride) with an excess of a diol, for example, adipic acid with ethylene glycol or butanediol, terephthalic acid or anhydride with ethylene glycol or butane diol, or by reacting a lactone with an excess of a diol such as reacting caprolactone with propylene glycol.
  • a dicarboxylic acid which may be an aliphatic or aromatic dicarboxylic acid or anhydride
  • a diol for example, adipic acid with ethylene glycol or butanediol, terephthalic acid or anhydride with ethylene glycol or butane diol
  • a lactone with an excess of a diol such as reacting caprolactone with propylene glycol.
  • Compounds additional to the polyisocyanate, polyol, and catalyst(s) may be present in the polyurethane reaction mixture.
  • Such compounds include release agents, fillers, colourants, cross-linkers, chain extenders, blowing agents, fungicides, waxes, impact modifiers, surfactants, plasticisers, water, coupling agents and fire retardants. This list is not exhaustive. The invention will be further described in the following examples.
  • Tetra-n-propoxy zirconium in n-propanol solution 14Og, 0.316 moles was placed in a rotary evaporator and 2-ethyl-1-hexanol (2-EHA) (82g, 0.63 moles) was added , followed by N 1 N- diethylacetoacetamide (DEAA) (99.4g, 0.63 moles). The mixture was stirred for 15-20 minutes at 70 0 C , then distilled under vacuum to remove all free n-propanol (111g). NMR analysis indicated a 100% product of Zr(O-CH 2 CH 2 (C 2 H 5 )C 4 Hg) 2 (OC(CH 3 )CHCON(C 2 H5)2)2.
  • N,N-diethylacetoacetamide (4 moles, 629g) was slowly added to a solution of zirconium(IV) propoxide (1 mole, 323g) in 1-propanol (2 moles, 12Og) at ambient temperature. The mixture was then stirred for an additional 15 minutes at 45°C before excess 1-propanol (5 moles, 30Og) is distilled off under reduced pressure at a temperature of 60 to 70 0 C. The resulting product contains Zr(OC(CH 3 )CHCON(C 2 H 5 ) 2 ) 4 (1mole) and approx 1 mole of 1-propanol. The propanol may be completely removed by recrystallising solid Zr(DEAA) 4 from toluene solution using heptane.
  • Example 3 N,N-diethylacetoacetamide (60 moles, 9.4 kg) was slowly added to a solution of zirconium(IV) propoxide (10 moles, 3.2kg) in 1 -propanol (20 moles, 1.2 kg) at ambient temperature. The mixture was then stirred for an additional 15 minutes at 45°C and all 1-propanol (48.6 moles, 2.9 kg) is distilled off under reduced pressure at a temperature of 60 to 70 0 C. The resulting product contains Zr(OC(CH 3 )CHCON(C 2 H 5 ) 2 ) 4 + free N,N-diethylacetoacetamide at a ratio of 1 mole : 2 moles.
  • Tetra-n-propoxy zirconium in n-propanol solution 90.8g, 0.205 moles was placed in a rotary evaporator and tert-butanol (30.3g, 0.41 moles) was added, followed by DEAA (64.5g, 0.41 moles). The mixture was stirred for 15-20 minutes at 70 0 C, then distilled under vacuum to remove all free n-propanol (73g). The resulting product contains Zr(O-C(CH 3 ) 3 ) 2 (OC(CH 3 )CHCON(C 2 H 5 ) 2 ) 2 .
  • Example 5 The catalysts of Examples 1 and 4 were used in a polyurethane casting formulation. 7Og of polyol (commercial mixture of a primary and secondary polyol) was placed in a speed mixer cup, mixed with the catalyst (based on polyol 3% or 5%), then mixed with 72.16 g of polyisocyanate prepolymer (DesmodurTM W, aliphatic isocyanate ( methylene bis(4-cyclohexyl isocyanate)) for 10 seconds. A portion of the mixture was then poured onto a surface at room temperature; the rest (approx 135 g) was left in the beaker also at room temperature (about 20 - 25 0 C). The gel time (time to no string) and tack free time was measured. The results are shown in Table 1.
  • the faster gel time and tack-free time in the beaker is due to the retention of heat from the exothermic reaction between the isocyanate and the polyol.
  • the heat can dissipate more easily because the coating is relatively thin compared with the mass in the beaker.
  • the catalyst made in Example 2 was used in the preparation of a rigid foam using a commercial polyol/polyisocyanate system.
  • the polyol (45g) was placed in a mixer cup with a blowing catalyst (bis(dimethylaminoethyl)ether (DMEA)) (0.27g) and the catalyst of the invention, mixed for 10 seconds and then an isocyanate (45g) was added.
  • DMEA bis(dimethylaminoethyl)ether
  • the mixture was placed in a beaker and the cream-time, string-time, time till the foam finished rising and tack-free time was observed.
  • DMEA bis(dimethylaminoethyl)ether
  • a commercial polyol (6000 MW) was mixed with the catalyst of Example 1 and then with a plasticiser / polyisocyanate mixture. The mixture was mixed a high speed for 10 seconds and left to cure at room temperature. A comparison using a commercial mercury-based gelling catalyst (ThorcatTM 535) was also run. The results are shown in Table 3.
  • VERTECTM NPZ tetra-n-propoxy zirconium in n-propanol (443g, 1 mole of metal) was placed into a reaction flask purged with nitrogen, fitted with a stirrer, thermometer, and condenser and mounted in a water bath. N,N-diethylacetoacetamide (314.42g, 2 mole) was added to the reactor via a dropping funnel whilst stirring and an exothermic reaction could be observed. N-Propanol (NPA) (225.65g, 3.76 mole) was removed form the product, Zr(DEAA) 2 (NPA) 2 , under reduced pressure (70°C/30"Hg).
  • VERTECTM NPZ (443g, 1mole) was placed into a reaction flask purged with nitrogen, fitted with a stirrer, thermometer, and condenser and mounted in a water bath.
  • N,N-diethylacetoacetamide (628.84g, 4 mole) was added to the reactor via a dropping funnel whilst stirring and an exothermic reaction could be observed.
  • Diethylene glycol (DEG) 106.12g, 1mole
  • N-Propanol (354g, 5.9mole) was removed form the product, Zr(DEAA) 4 + DEG, under reduced pressure (70°C/30"Hg).
  • VERTECTM NPZ (100.0Og, 0.2272 mol) was placed into a reaction flask, fitted with a condenser and mounted in a temperature controlled water bath. While spinning the flask, N 1 N- diethylacetoacetamide (71.46g, 0.4544 mol) was added to the reactor via a dropping funnel, this was left to blend for IOmins at which point a slight exotherm was noticed. Then 1 ,3-propanediol (17.3Og, 0.2272mol) was added drop-wise to the reactor and blended for a further IOmins. N-propanol (68.29g, 1.14mol) was removed from the product, Zr(DEAA) 2 (1 ,3-propanediol), under reduced pressure (87°C/29" Hg). Example 11 Shelf life tests
  • 0.1 % catalyst was added to a commercial polyester polyol, mixed and allowed to age at 40 0 C for 0, 4 and 7 days before reacting the polyol containing the catalyst with a commercial modified MDI polyisocyanate. The formulation was then poured into a preheated aluminium dish and allowed to cure at 80 0 C during which time the hardness was measured at intervals up to one hour. The results are shown in Table 4.

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Abstract

The invention comprises a catalyst compound of formula Zr(L)(A1 )(A2)(A3) where L represents a ketoamide ligand, A1, A2 & A3 may be the same or different and each represent a ligand derived from a compound selected from the group consisting of:- an alcohol, a polyol, an alkyl acetoacetate, a diketone, a ketoamide, a carboxylic acid or ester thereof, an alkanolamine, a phosphoric acid ester and a sulphonic acid or ester thereof. The compound may be made by the reaction of a zirconium alkoxide or haloalkoxide with a ketoamide. The compound is useful as a catalyst for the reaction of a polyisocyanate with a hydroxyl-containing compound, e.g. for the manufacture of polyurethanes or composite cellulosic materials such as fibre-boards.

Description

Novel zirconium compound, catalyst and its use for polyurethane manufacture
The present invention concerns a novel catalyst comprising a zirconium chelate, and its use to catalyse the reaction of an isocyanate-containing compound with an alcohol or an amine to form a polyurethane or a polyurea.
Polyurethanes are typically made by reacting a polyisocyanate compound with a polyol in the presence of an organometallic catalyst. Catalysts for polyurethane manufacture are conventionally based on tin compounds such as dibutyl tin dilaurate or compositions of mercury such as phenyl mercuric neodecanoate. More recently, compounds based upon metals such as titanium or nickel have been used.
Compounds of titanium, zirconium, hafnium, iron (III), cobalt (III) or aluminium were described in WO2004/044027. Such compounds are of general formula RO-M(L1)X (L2)y(L3)z where R is alkyl or a hydroxy-alkyl, hydroxyalkoxyalkyl, or (hydroxy)polyoxyalkyl group and up to 2 of L1 to L3 may represent an amide of acetoacetic acid. These compounds have a single labile -OR ligand and were believed to function as a cure catalyst by exchange or insertion of the polyol or of the isocyanate at the labile site on the organometallic composition, by displacement of the OR group.
US-A-5846897 discloses zirconium compounds with diketones or alkylacetoacetates which catalyse the isocyanate - alcohol reaction having the chemical structure: Me (X1 , X2, X3, X4) wherein Me is zirconium (Zr) or hafnium (Hf) and X1 , X2, X3, and X4, are the same or different and selected from the group consisting of a diketone and an alkylacetoacetate having the structures: RICOCH2COR2 and RIOCOCH2COR2 wherein each of R1 and R2 is a branched or linear C1 -C20 hydrocarbon and at least one of X1 , X2, X3, and X4 is a diketone with structure (II) wherein the total number of carbons in R1 + R2 is at least 4. Patil et al (J. Mater Chem 2003, 13, 2177 - 2184) have used zirconium bis(isopropoxide)bis(N,N- diethylacetoacetamide) as a precursor for the metal-organic chemical vapour deposition of zirconium dioxide.
It is an object of the invention to provide an alternative catalyst for making polyurethanes.
The catalyst is of formula Zr(L)(A1 )(A2)(A3) where L represents a ketoamide ligand, A1, A2& A3 may be the same or different and each represent a ligand derived from a compound selected from the group consisting of:- an alcohol, a polyol, an alkyl acetoacetate, a diketone, a ketoamide, a carboxylic acid or ester thereof, an alkanolamine, a phosphoric acid ester and a sulphonic acid or ester thereof; provided that either: (i) none of A1, A2& A3 represent a ligand -OR where R is alkyl or a hydroxy-alkyl, hydroxyalkoxyalkyl, or (hydroxy)polyoxyalkyl group, or
(ii) at least two of A1, A2 & A3 represent a ligand -OR where R is alkyl or a hydroxy- alkyl, hydroxyalkoxyalkyl, or (hydroxy)polyoxyalkyl group. In this specification, we refer to "a ligand derived from" a compound in the sense that the ligand has been formed by the reaction of the compound with a zirconium compound to form the claimed catalyst or a precursor thereto. Thus, for example, a ligand derived from an alcohol ROH is present in the catalyst as an alkoxide RO-, and a ligand derived from a carboxylic acid RCOOH is present in the catalyst as a carboxylate RCOO-. The skilled person will therefore understand that the compounds referred to as forming a ligand L or A will be present in the catalyst in their reacted form and generally not in the unreacted form of the compound. Most of the ligand-forming compounds herein react with a zirconium compound though a reactive -OH to form an -0-Zr- linkage in the catalyst.
The ketoamide ligand, L, is derived from a ketoamide of general structure shown in Formula 1 , which is believed to react with the zirconium alkoxide or haloalkoxide through its "enol" form, shown in Formula 1', to form a ligand R1R2COCR3CR4O-.
Figure imgf000003_0001
Formula 1 Formula 1'
In Formula 1 & 1', R1, R2 and R4 are independently selected from H, linear or branched alkyl or aryl. When R1, R2 and/or R4 are alkyl groups, they preferably contain from 1 to 22 carbon atoms, more preferably from 1 to 8 C atoms. When R1, R2 and/or R4 are aryl groups, they may be unsubstituted or substituted with alkyl, halogen or ether groups. By "aryl" we include polycyclic aromatic groups. It is preferred that R1, R2 and/or R4 are not H, and tertiary amides, i.e. where neither R1 nor R2 is H are preferred. R3 is selected from H or linear or branched alkyl, preferably containing from 1 to 22 carbon atoms, more preferably from 1 to 8 C atoms.
L is preferably a ligand derived from a N,N-dialkyl acetoacetamide (DAAA) and a preferred dialkyl acetoacetamide comprises N,N-diethylacetoacetamide (DEAA). Other suitable ketoamides include acetoacetanilide, o-acetoacetaniside, 2'-benzoylacetanilide, 4'- chloroacetoacetanilide, p-acetoacetaniside, N,N-dimethylacetoacetamide,
N-methylacetoacetamide, N-ethylacetoacetamide, N-(2-acetamidophenethyl)-1 -hydroxy-2- naphthamide, 2',5'-dichloroacetoacetanilide, 2',4'-dimethylacetoacetanilide and 2-methylacetoacetanilide. The reaction product may contain more than 1 mole of ketoamide per mole of zirconium when at least one of A1, A2& A3 is derived from a ketoamide. The product may contain up to four moles of ketoamide bound to the zirconium atom to form a chelate. Each ketoamide ligand may be the same as or different from each other ketoamide ligand. In a preferred composition containing 2 or 4 ketoamide ligands, each ketoamide ligand is derived from the same ketoamide compound. The product may also contain a free ketoamide compound, i.e. there may be more than 4 moles of ketoamide per mole of zirconium. In one embodiment, the catalyst is a composition comprising from 1 to 10 moles, more preferably from 2 to 4 moles, of free ketoamide per mole of zirconium. One preferred such embodiment comprises a composition of formula [Zr(DEAA)4 + 2DEAA]. For convenience, when we refer to Zr(DEAA)X, this means that the zirconium compound has x ligands derived from DEAA, which is present in the catalyst in its reacted form.
A1, A2 & A3 may be the same or different and each represent a ligand derived from a compound selected from the group consisting of an alcohol, a polyol, an alkyl acetoacetate, a diketone, a ketoamide, a carboxylic acid or ester thereof, an alkanolamine or a phosphoric acid ester. The alcohol is of general formula R-OH where R is an alkyl or aryl (including polyaryl) group. Where R is aryl, we include phenol, napthol and substituted versions of these, e.g. alkylphenols such as dodecylphenol. Preferably R is alkyl, more preferably an alkyl group containing from 1 to 12 C atoms, and most preferably an alkyl group containing from 2 to 8 C atoms. When more than one of A1, A2& A3 is derived from an alcohol then each R may or may not be the same as the other(s). Preferred alcohols include, ethanol, isopropanol, n-propanol, tertiary butanol, n- butanol, 2-ethylhexanol, amyl alcohol, tert-amyl alcohol, hexanol, cyclohexanol, phenol, dodecylphenol and naphthol. The alcohol reacts with a zirconium compound to form an alkoxide or aryloxide RO- ligand. When only one of A1, A2 & A3 is derived from an alcohol, then the alcohol is not a singly-functionalised alkyl alcohol, R-OH where R is alkyl. When more than one of A1, A2& A3 is derived from an alcohol, then either none of them is a singly-functionalised alkyl alcohol, R-OH where R is alkyl or alternatively at least two of them is a singly- functionalised alkyl alcohol, R-OH where R is alkyl. Compounds disclosed in WO-A-
2004/044027 are thereby excluded from the scope of this invention. The compounds disclosed in WO-A-2004/044027 all have a single labile alkoxy ligand which provides an active site for catalysis. In one preferred embodiment of the invention, the catalyst has the general formula Zr(ketoamide)2(OR)2 where R is alkyl, more preferably an alkyl group containing from 1 to 12 C atoms, and most preferably an alkyl group containing from 2 to 8 C atoms. As examples of such compounds, we include Zr(DEAA)2(2-ethylhexoxide)2, Zr(n-butoxide)2(DEAA)2, Zr(n- propoxide)2(DEAA)2, Zr(DEAA)2(tert-amylalkoxide)2 and Zr(isopropoxide)2(DEAA)2. The polyol may be a monomeric alcohol having more than one hydroxy group, for example ethylene glycol, 1 ,3-propylene glycol, 1 ,4-butane diol, or a dimeric or polymeric alcohol such as diethylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol. The polyol also includes polyester polyols and polyether polyols of the type typically used in the manufacture of poyurethanes and which are commercially available. Hydroxy- functionalised resins may also be suitable for forming one or more of the A ligands in general formula 1. Such resins include hydroxyl-containing resins which are sold for use in printing inks, preferably having a hydroxyl number of from about 100 to about 500, especially from about 200 to about 400 mg KOH/g (tested according to DIN 53 240). Examples of suitable synthetic resins include ketone- aldehyde resins especially ketone-formaldehyde resins such as hydrogenated acetophenone formaldehyde condensation resins, cyclohexanone-formaldehyde condensation resins and urethane-modified ketone aldehyde resins. Such resins are available from Degussa AG as Synthetic Resins 1201 , CA and SK, for example.
When a polyol is used it is likely to bond to the zirconium as a multidentate ligand so that more than one of A1, A2 & A3 may be represented by the same molecule, i.e. A1, A2 and/or A3 may be linked together. When such a multidentate ligand is used, each molecule may bond multiply to the same zirconium atom or alternatively it may bond to more than one zirconium atom to form a bridge between the zirconium atoms. It is likely that in such compounds there is a mixture containing bridged and non-bridged structures. In a preferred embodiment of the catalyst involving such a multidentate ligand, the catalyst is of general formula Zr(ketoamide)2(polyol) and/or Zr2(ketoamide)4(polyol)2 and/or higher oligomeric bridged structures where (polyol) is in each case a ligand derived from the polyol by reaction of two hydroxy functions with zirconium to form two alkoxide bonds. References to any Zr(L) (A)(polyol) compound therefore refer to the empirical formula and include compounds in which bridged dimeric and oligomeric forms are present. Preferred examples of this type include Zr(DEAA)2(1 ,3-propanedioxide), Zr(DEAA)2(1 ,4-butanedioxide) and Zr(DEAA)2(diethyleneglycoxide).
A1, A2 and/or A3 may each represent a ligand derived from an alkyl acetoacetate, i.e. an ester of an alkyl alcohol R5OH with acetoacetic acid wherein R5 is a branched or linear C1 -C20 hydrocarbon; more preferably R5 contains from 1 to 8 carbon atoms. Ethylacetoacetate (EAA) is a particularly preferred alkyl acetoacetate compound. When we refer to Zr(EAA)n, we mean a zirconium compound having n ligands derived from ethylacetoacetate.
A1, A2 and/or A3 may each represent a ligand derived from a diketone which is preferably a β- diketone of general formula R6COCH2COR7 wherein each of R6 and R7 is a branched or linear C1 -C20 hydrocarbon. Preferred diketones include acetylacetone (2,4-pentanedione), 2,4- heptanedione and alkyl-substituted versions thereof and 3,5-heptanedione and alkyl-substituted versions thereof. A1, A2 and/or A3 may each represent a ligand derived from a carboxylic acid or ester thereof. Suitable carboxylic acids include benzoic acid and alkyl carboxylic acids, for example a C2 - C30 carboxylic acid, especially a C4 - C22 carboxylic acid such as butyric, neodecanoic, stearic, isostearic, oleic or 2-ethyl-hexylcarboxylic acid. The carboxylic acid or ester may contain more than one carboxylic acid group such as malonic acid, tartaric acid and their esters, especially alkyl esters e.g. diethyl malonate. Hydroxycarboxylic acids such as lactic acid, citric acid, oxalic acid may also form suitable ligands with zirconium.
A1, A2 and/or A3 may each represent a ligand derived from an alkanolamine, i.e. a compound of general formula HO(CH2)XNR8 2 where R8 comprises HO(CH2)X or an alkyl group or hydrogen. X is an integer and preferably ranges from 1 to 8. Preferred alkanolamines include ethanolamine, diethanolamine and triethanolamine although others are suitable.
A1, A2 and/or A3 may each represent a ligand derived from an organophosphorus compound having a P-OH group, particularly a phosphate ester, i.e. an alkyl or aryl acid phosphate, or a salt thereof comprising a dialkyl phosphate, a diaryl phosphate, a monoalkyl phosphate, a monoaryl phosphate or a mixture of two or more of a dialkyl phosphate, a diaryl phosphate, a monoalkyl phosphate and a mono aryl phosphate, a phosphonate ester or a salt thereof comprising an alkyl or aryl phosphonate or salts thereof, an alkyl or aryl pyrophosphate, an alkyl or aryl phosphonic acid or alkyl or aryl ester thereof or a salt thereof, a dialkyl or aryl phosphinic acid or salt thereof. In all cases the organophosphorus compound contains a P-OH group, i.e. an acidic group or its salt, i.e. a P-O"M+ group where M is metal or ammonium. Preferred organophosphorus compounds comprise an alkyl phosphate compound which may be a mono- or a di-alkyl phosphate or is conveniently a mixture of mono- and dialkyl phosphates, such mixtures being more readily available than pure mono- or a di-alkyl phosphates. Monoalkyl phosphates generally have a formula (R9O)PO(OH)2. Dialkyl phosphates generally have the formula (R9O)(R10O)PO(OH). R9, R10 may be the same or different and represent a linear or branched alkyl group usually containing up to 8 carbon atoms and preferably containing up to 5 carbon atoms. Usually, but not necessarily, R9,and R10 are identical. Preferably R9, and R10 are selected from n-butyl, sec-butyl, ferf-butyl, /so-propyl, n-propyl, ethyl, methyl, phenyl, amyl and ethyl-hexyl.
Suitable phosphonate ester, phosphonic acid, phosphinic acid or salt thereof comprises an alkyl or aryl phosphonate, phosphonic acid or their salts and generally have a formula
(R11)nPO(OR12)2-n(OH), where R11 and R12 each represent a hydrogen atom or an aryl group or an alkyl group containing up to 8 carbon atoms and preferably containing up to 5 carbon atoms and n is 1 or 2. A1, A2 and/or A3 may each represent a ligand derived from a sulphonic acid or ester thereof, i.e. a compound of general formula R13SO3H or its ester where R is aryl or alkyl. Examples of suitable sulphonic acids include methane sulphonic acid and substituted benzene sulphonic acids such as dodecylbenzene sulphonic acid. Salts of these sulphonic acids are also suitable, for example alkali metal salts such as the sodium salt and quaternary ammonium salts.
The catalyst of the invention preferably comprises the reaction product of a zirconium alkoxide or haloalkoxide with a ketoamide compound and optionally with at least one other ligand- forming compound. The compounds of the invention may be made by reacting a zirconium compound such as an alkoxide, a halide or haloalkoxide with the ketoamide and then with the other compound(s) to form the A ligands if necessary. Where the A-ligands are alkoxide, these may form part of the starting zirconium compound. When mixed alkoxide ligands are required this may be achieved by reacting the alcohol forming a more stable alkoxide with the alkoxide of the first alcohol so that some of the first alcohol is displaced from the original compound to form the mixed alkoxide. The reaction of n moles of the ketoamide or of a compound forming the A ligand with a zirconium alkoxide or haloalkoxide produces n moles of alcohol or of a hydrogen halide derived from the zirconium alkoxide or haloalkoxide. When an alcohol is produced in such a reaction it may be removed from the product, usually by distillation or it may remain in the product as a free alcohol if desired.
Zirconium haloalkoxides may be represented by the formula Zr(OR)x. B(4-X) where R is an alkyl group as described above, B represents a halide and x is a number from 0 to less than 4. The haloalkoxides may be of mixed formulation and therefore x need not be an integer. The preferred halides are chloride and bromide, particularly chloride.
Preferably the zirconium alkoxide or haloalkoxide is a zirconium alkoxide of formula Zr(OR)4, where R has the meaning described above. Each R may or may not be the same as each other R. In one embodiment, the zirconium alkoxide is a tetra-alkyl alkoxide where all alkoxide groups are the same. Preferred zirconium alkoxides include tetra-i-propoxy zirconium, tetra- ethyl zirconium, tetra-n-propoxy zirconium and tetra-n-butoxy zirconium since these are readily available commercial materials. In an alternative embodiment the zirconium alkoxide is a mixed alkoxide. This embodiment is particularly useful where one or more of the OR groups is derived from an alkoxide which is less readily available. In such a case, a tetra alkoxy zirconium compound Zr(OR)4 may be reacted with an alcohol R'OH to form a mixed alkoxide Zr(OR)y(OR')z, where y and z may vary from 1 to 3 and y + z = 4. When reacted with less than 4 moles of the ketoamide, the more easily displaced alcohol of ROH and R'OH will be replaced first to give products of the form Zr(L)x(OR') (4_x) if ROH is more readily displaced than R'OH. Suitable zirconium alkoxides may therefore comprise Zr(isopropoxide)2(2-ethylhexoxide)2, Zr(n- butoxide)2(2-ethylhexoxide)2, Zr(n-butoxide)2(tert-amylalkoxide)2, Zr(isopropoxide)2(tert- amylalkoxide)2.
The catalyst composition may additionally comprise a solvent or diluent. The solvent or diluent may be a compound that coordinates with the zirconium catalyst or it may be non-coordinating. The solvent may comprise an alcohol (which may be alcohol liberated in the reaction of a zirconium alkoxide with the ketoamide). Suitable solvents include polyols (e.g. a similar polyol to that used in a polyurethane reaction for which the compound is used as catalyst), such as 1 ,4-butane diol, 1 ,3-propylene glycol, ethylene glycol, diethylene glycol, a polyethylene glycol, a polypropylene glycol, a polyester polyol, a ketoamide, particularly the ketoamide used to form the catalyst, ethylacetoacetate, acetylacetone, diethylmalonate or an excess of a compound used to form one of the A ligands.
Examples of preferred catalysts comprise compounds of the following formulae:- Zr(DEAA)2(2- ethylhexoxide)2, Zr(n-butoxide)2(DEAA)2, Zr(n-propoxide)2(DEAA)2, Zr(DEAA)2(tert- amylalkoxide)2, Zr(isopropoxide)2(DEAA)2, Zr(DEAA)4 , Zr(t-butoxide)2(DEAA)2, Zr(DEAA)4,
Zr(DEAA)2(propanedioxide)2, Zr(DEAA)2(diethyleneglycoxide)2,
Zr(DEAA)2(ethylacetoacetato)2,Zr(DEAA)2(2,4-pentanedionato)2,Zr(DEAA)2(diethylmalonate)2
Zr(DEAA)2(1 ,3-propanediol) Zr(DEAA)2(1 ,4-butanediol) and Zr(DEAA)2(diethyleneglycol). These catalysts may also include additional quantities of at least one of the ligand-forming compounds which are assumed to be present in a non-complexed state. In particular free
DEAA, ethylacetoacetate, acetylacetone or polyol, especially diethylene glycol has been found to be of benefit.
In a preferred embodiment, the catalyst does not comprise a compound of bismuth as a co- catalyst.
The catalyst composition is useful in the manufacture of polyurethanes, i.e. as a cure catalyst for the reaction of a polyisocyanate with a compound containing an active hydrogen, especially a hydroxyl group, in particular a a polyol; or an amino compound. Applications of such polyurethanes are very diverse and include mouldings, foams, adhesives, coatings, cast or spray elastomers, casting resins etc. The catalyst composition may also be used to catalyse the reaction of a polyisocyanate binder with hydrous materials such as those derived from wood or plant fibres, e.g. as used in the manufacture of composite boards for the construction industry.
Any organic polyisocyanate compound or mixture of organic polyisocyanate compounds may be suitable provided said compounds have at least 2 isocyanate groups. Organic polyisocyanates include diisocyanates, particularly aromatic diisocyanates, and isocyanates of higher functionality. Examples of organic polyisocyanates include aliphatic isocyanates such as hexamethylene diisocyanate; and aromatic isocyanates such as m- and p-phenylene diisocyanate, tolylene-2,4- and tolylene- 2,6-diisocyanate, diphenylmethane-4,4'-diisocyanate, chlorophenylene- 2,4-diisocyanate, naphthylene-1 ,5-diisocyanate, diphenylene-4,4'- diisocyanate, 4,4'-diisocyanate-3,3'-dimethyl-diphenyl, 3-methyldiphenylmethane-4,4'-di- isocyanate and diphenyl ether diisocyanate; and cycloaliphatic diisocyanates such as cyclohexane-2,4- and -2,3-diisocyanate, 1-methylcyclohexyl-2,4- and -2,6-diisocyanate and mixtures thereof and bis-(isocyanatocyclohexyl)methane and tri isocyanates such as 2,4,6- triisocyanatotoluene and 2,4,4-tri- isocyanatodiphenylether. Modified polyisocyanates containing isocyanurate, carbodiimide or uretonimine groups may be used and are generally chosen when particular physical properties are desired. Blocked polyisocyanates, like the reaction product of a phenol or an oxime and a polyisocyanate, may be used, where they have a deblocking temperature below the temperature applied in use. The organic polyisocyanate may also be an isocyanate-ended prepolymer made by reacting an excess of a diisocyanate or higher functionality polyisocyanate with a polyol such as, for example a polyether polyol or a polyester polyol. Water-emulsifiable organic polyisocyanates like those described in UK patent no. 1 444 933, in European patent publication no. 516 361 and in PCT patent publication no. 91/03082 can also be used.
Mixtures of isocyanates may be used, for example a mixture of tolylene diisocyanate isomers such as the commercially available mixtures of 2,4- and 2,6-isomers and also the mixture of di- and higher polyisocyanates. Mixtures of diisocyanates known commercially as "crude MDI", contain about 60% of 4,4'-diphenylmethane diisocyanate along with other isomeric and analogous higher polyisocyanates. Polyisocyanate mixtures may optionally contain monofunctional isocyanates such as p-ethyl phenylisocyanate. Such mixtures are well-known in the art and include the crude phosgenation products containing methylene bridged polyphenyl polyisocyanates, including diisocyanate, triisocyanate and higher polyisocyanates together with any phosgenation by-products.
Preferred isocyanates are those wherein the isocyanate is an aromatic diisocyanate or polyisocyanate of higher functionality such as a pure diphenylmethane diisocyanate or a mixture of methylene bridged polyphenyl polyisocyanates containing diisocyanates, tri isocyanates and higher functionality polyisocyanates. Methylene bridged polyphenyl polyisocyanates are well known in the art. They are prepared by phosgenation of corresponding mixtures of polyamines. For convenience, polymeric mixtures of methylene bridged polyphenyl polyisocyanates containing diisocyanate, triisocyanate and higher functionality polyisocyanates are referred to hereinafter as polymeric MDI. Polyisocyanates suitable for use with the organometallic complexes of the invention include SUPRASEC™ DNR, SUPRASEC™ 2185, RUBINATE™ M and RUBINATE™ 1840, all available from Huntsman Polyurethanes. Preferably the polyisocyanate is liquid at room temperature. Suitable polyisocyanates are well known in the art.
The polyol component may be any suitable for the manufacture of polyurethanes and includes polyester-polyols, polyester-amide polyols, polyether-polyols, polythioetherpolyols, polycarbonate polyols, polyacetal polyols, polyolefin polyols polysiloxane polyols, dispersions or solutions of addition or condensation polymers in polyols of the types described above, often referred to as "polymer" polyols. A very wide variety of polyols has been described in the prior art and is well known to the formulator of polyurethane materials.
Typically, a mixture of polyols is used to manufacture polyurethane having particular physical properties. The polyol or polyols is selected to have a molecular weight, backbone type and hydroxy functionality which is tailored to the requirements of the formulator. Typically the polyol includes a chain extender, which is often a relatively short-chain diol such as 1 ,4-butane diol or diethylene glycol or a low molecular weight polyethylene glycol. Alternative chain extenders in commercial use, such as diamines, e.g. MOCA (4,4-methylene bis (2-chloroaniline)) may also be used.
Suitable polyols include the polyalkylene ether- and polyester-polyols. The polyalkylene ether polyols include the poly(alkylene oxide) polymers such as poly( ethylene oxide) and poly(propylene oxide) polymers and copolymers with terminal hydroxyl groups derived from polyhydric compounds, including diols and triols; for example, among others, ethylene glycol, propylene glycol, 1 ,3-butane diol, 1 ,4-butane diol, 1 ,6-hexane diol, neopentyl glycol, diethylene glycol, dipropylene glycol, pentaerythritol, glycerol, diglycerol, trimethylol propane and like low molecular weight polyols. High molecular weight polyether polyol may be used. Also, mixtures of high molecular weight polyether polyols such as mixtures of di- and tri-functional materials optionally with lower molecular weight or different chemical composition materials may be used. Useful polyester polyols include polylactones, e.g. polycaprolactone, and those produced by reacting a dicarboxylic acid (which may be an aliphatic or aromatic dicarboxylic acid or anhydride) with an excess of a diol, for example, adipic acid with ethylene glycol or butanediol, terephthalic acid or anhydride with ethylene glycol or butane diol, or by reacting a lactone with an excess of a diol such as reacting caprolactone with propylene glycol.
Compounds additional to the polyisocyanate, polyol, and catalyst(s) may be present in the polyurethane reaction mixture. Such compounds include release agents, fillers, colourants, cross-linkers, chain extenders, blowing agents, fungicides, waxes, impact modifiers, surfactants, plasticisers, water, coupling agents and fire retardants. This list is not exhaustive. The invention will be further described in the following examples.
Example 1
Tetra-n-propoxy zirconium in n-propanol solution (14Og, 0.316 moles) was placed in a rotary evaporator and 2-ethyl-1-hexanol (2-EHA) (82g, 0.63 moles) was added , followed by N1N- diethylacetoacetamide (DEAA) (99.4g, 0.63 moles). The mixture was stirred for 15-20 minutes at 70 0C , then distilled under vacuum to remove all free n-propanol (111g). NMR analysis indicated a 100% product of Zr(O-CH2CH2(C2H5)C4Hg)2 (OC(CH3)CHCON(C2H5)2)2.
Example 2
N,N-diethylacetoacetamide (4 moles, 629g) was slowly added to a solution of zirconium(IV) propoxide (1 mole, 323g) in 1-propanol (2 moles, 12Og) at ambient temperature. The mixture was then stirred for an additional 15 minutes at 45°C before excess 1-propanol (5 moles, 30Og) is distilled off under reduced pressure at a temperature of 60 to 700C. The resulting product contains Zr(OC(CH3)CHCON(C2H5)2)4 (1mole) and approx 1 mole of 1-propanol. The propanol may be completely removed by recrystallising solid Zr(DEAA)4 from toluene solution using heptane.
Example 3 N,N-diethylacetoacetamide (60 moles, 9.4 kg) was slowly added to a solution of zirconium(IV) propoxide (10 moles, 3.2kg) in 1 -propanol (20 moles, 1.2 kg) at ambient temperature. The mixture was then stirred for an additional 15 minutes at 45°C and all 1-propanol (48.6 moles, 2.9 kg) is distilled off under reduced pressure at a temperature of 60 to 700C. The resulting product contains Zr(OC(CH3)CHCON(C2H5)2)4 + free N,N-diethylacetoacetamide at a ratio of 1 mole : 2 moles.
Example 4
Tetra-n-propoxy zirconium in n-propanol solution (90.8g, 0.205 moles) was placed in a rotary evaporator and tert-butanol (30.3g, 0.41 moles) was added, followed by DEAA (64.5g, 0.41 moles). The mixture was stirred for 15-20 minutes at 70 0C, then distilled under vacuum to remove all free n-propanol (73g). The resulting product contains Zr(O-C(CH3) 3)2 (OC(CH3)CHCON(C2H5)2)2.
Example 5 The catalysts of Examples 1 and 4 were used in a polyurethane casting formulation. 7Og of polyol (commercial mixture of a primary and secondary polyol) was placed in a speed mixer cup, mixed with the catalyst (based on polyol 3% or 5%), then mixed with 72.16 g of polyisocyanate prepolymer (Desmodur™ W, aliphatic isocyanate ( methylene bis(4-cyclohexyl isocyanate)) for 10 seconds. A portion of the mixture was then poured onto a surface at room temperature; the rest (approx 135 g) was left in the beaker also at room temperature (about 20 - 25 0C). The gel time (time to no string) and tack free time was measured. The results are shown in Table 1.
Table 1
Figure imgf000012_0001
The faster gel time and tack-free time in the beaker is due to the retention of heat from the exothermic reaction between the isocyanate and the polyol. When the mixture is cured as a coating on a surface the heat can dissipate more easily because the coating is relatively thin compared with the mass in the beaker.
Example 6
The catalyst made in Example 2 was used in the preparation of a rigid foam using a commercial polyol/polyisocyanate system. The polyol (45g) was placed in a mixer cup with a blowing catalyst (bis(dimethylaminoethyl)ether (DMEA)) (0.27g) and the catalyst of the invention, mixed for 10 seconds and then an isocyanate (45g) was added. The mixture was placed in a beaker and the cream-time, string-time, time till the foam finished rising and tack-free time was observed. The results are shown in Table 2, together with a comparison in which the catalyst of the invention was replaced by a commercial gelling catalyst (DABCO™33LV).
Table 2
Figure imgf000012_0002
Example 7
A commercial polyol (6000 MW) was mixed with the catalyst of Example 1 and then with a plasticiser / polyisocyanate mixture. The mixture was mixed a high speed for 10 seconds and left to cure at room temperature. A comparison using a commercial mercury-based gelling catalyst (Thorcat™ 535) was also run. The results are shown in Table 3.
Table 3
Figure imgf000013_0001
Example 8
VERTEC™ NPZ (tetra-n-propoxy zirconium in n-propanol) (443g, 1 mole of metal) was placed into a reaction flask purged with nitrogen, fitted with a stirrer, thermometer, and condenser and mounted in a water bath. N,N-diethylacetoacetamide (314.42g, 2 mole) was added to the reactor via a dropping funnel whilst stirring and an exothermic reaction could be observed. N-Propanol (NPA) (225.65g, 3.76 mole) was removed form the product, Zr(DEAA)2(NPA)2 , under reduced pressure (70°C/30"Hg).
Example 9
VERTEC™ NPZ (443g, 1mole) was placed into a reaction flask purged with nitrogen, fitted with a stirrer, thermometer, and condenser and mounted in a water bath. N,N-diethylacetoacetamide (628.84g, 4 mole) was added to the reactor via a dropping funnel whilst stirring and an exothermic reaction could be observed. Diethylene glycol (DEG) (106.12g, 1mole) was added to the reactor via a dropping funnel whilst stirring and no exothermic reaction was observed. N-Propanol (354g, 5.9mole) was removed form the product, Zr(DEAA)4 + DEG, under reduced pressure (70°C/30"Hg).
Example 10
VERTEC™ NPZ (100.0Og, 0.2272 mol) was placed into a reaction flask, fitted with a condenser and mounted in a temperature controlled water bath. While spinning the flask, N1N- diethylacetoacetamide (71.46g, 0.4544 mol) was added to the reactor via a dropping funnel, this was left to blend for IOmins at which point a slight exotherm was noticed. Then 1 ,3-propanediol (17.3Og, 0.2272mol) was added drop-wise to the reactor and blended for a further IOmins. N-propanol (68.29g, 1.14mol) was removed from the product, Zr(DEAA)2(1 ,3-propanediol), under reduced pressure (87°C/29" Hg). Example 11 Shelf life tests
0.1 % catalyst was added to a commercial polyester polyol, mixed and allowed to age at 40 0C for 0, 4 and 7 days before reacting the polyol containing the catalyst with a commercial modified MDI polyisocyanate. The formulation was then poured into a preheated aluminium dish and allowed to cure at 800C during which time the hardness was measured at intervals up to one hour. The results are shown in Table 4.
Table 4
Figure imgf000014_0001
The results show that the catalysts of the invention remain active for curing the polyurethane reaction after mixing with polyol for at least several days. A prior art catalyst described in US5965686, Zr(EAA)4, was made by reacting 4 moles of ethylacetoacetate with VERTEC NPZ and removing the resulting n-propanol from the reaction mixture. This catalyst is active when it is first mixed with the polyol but appears to lose activity when allowed to age in contact with the polyol. The improved shelf-life of the catalysts of the invention allows the polyurethane manufacturer greater process flexibility.

Claims

Claims
1. A catalyst compound of formula Zr(L)(A1)(A2)(A3) where L represents a ketoamide ligand, A1, A2 & A3 may be the same or different and each represent a ligand derived from a compound selected from the group consisting of:- an alcohol, a polyol, an alkyl acetoacetate, a diketone, a ketoamide, a carboxylic acid or ester thereof, an alkanolamine, a phosphoric acid ester and a sulphonic acid or ester thereof; provided that either:
(i) none of A1, A2& A3 represent a ligand -OR where R is alkyl or a hydroxy-alkyl, hydroxyalkoxyalkyl, or (hydroxy)polyoxyalkyl group, or ( (iiii)) aatt lleeaasstt ttwwoo ooff AA11,, AA22 && AA33 rreepprreesseenntt aa lliiggaarnd -OR where R is alkyl or a hydroxy- alkyl, hydroxyalkoxyalkyl, or (hydroxy)polyoxyalkyl group.
2. A catalyst as claimed in claim 1 , wherein L represents a ketoamide ligand of general structure shown in Formula 1"
O σ
R2 R3
Formula 1" in which R1, R2 and R4 are independently selected from H, linear or branched alkyl or aryl wherein said aryl groups, may be unsubstituted or substituted with alkyl, halogen or ether groups and R3 is selected from H or linear or branched alkyl.
3. A catalyst as claimed in claim 1 or claim 2, wherein R1, R2 and/or R4 are alkyl groups containing from 1 to 22 carbon atoms, and R3 is H.
4. A catalyst as claimed in claim 3, wherein R1, R2 and/or R4 are alkyl groups containing from 1 to 8 carbon atoms, and R3 is H.
5. A catalyst as claimed in claim 4, wherein said ketoamide comprises N,N-diethylacetoacetamide.
6. A catalyst as claimed in any one of the preceding claims, wherein at least one of A1, A2 & A3 is derived from an alcohol of general formula R-OH where R is an alkyl group containing from 1 to 12 C atoms or an aryl, substituted aryl or polyaryl group.
7. A catalyst as claimed in any one claims 1 - 6, wherein at least one of A1, A2 & A3 is derived from a ketoamide.
8. A catalyst as claimed in claim 7, having the general formula Zr(ketoamide)2(OR)2 where each R is the same or different and is an alkyl group containing from 1 to 12 C atoms or an aryl, substituted aryl or polyaryl group.
9. A catalyst as claimed in claim 8 wherein the catalyst does not consist of Zr(DEAA)2(isopropoxide)2 where DEAA represents a ligand derived from N1N- diethylacetoacetamide.
10. A catalyst as claimed in any one of claims 1 - 7, wherein at least one of A1, A2 & A3 is derived from an alcohol having more than one hydroxy group.
11. A catalyst as claimed in claim 10, wherein the alcohol comprises ethylene glycol, 1 ,3- propylene glycol, 1 ,4-butane diol, diethylene glycol, dipropylene glycol, polyethylene glycol, polypropylene glycol a polyester polyol, a polyether polyol or a hydroxy- functionalised resin.
12. A catalyst as claimed in claim 10 or claim 11 , wherein the alcohol bonds to the zirconium as a multidentate ligand such that A1, A2 and/or A3 are linked together.
13. A catalyst as claimed in any one of claims 10 -12, wherein the catalyst is of general formula Zr(ketoamide)2(polyol) including compounds in which bridged dimeric and oligomeric forms are present.
14. A catalyst as claimed in any one of claims 1 - 7 or 10 - 12, wherein at least one of A1, A2 & A3 is derived from an alkyl acetoacetate.
15. A catalyst as claimed in any one claims 1 - 7 or 10 - 12, wherein at least one of A1 , A2 & A3 is derived from a diketone.
16. A catalyst as claimed in any one claims 1 - 7 or 10 - 12, wherein at least one of A1, A2& A3 is derived from a carboxylic acid or ester thereof.
17. A catalyst as claimed in any one claims 1 - 7 or 10 - 12, wherein at least one of A1, A2 & A3 is derived from an alkanolamine.
18. A catalyst as claimed in any one claims 1 - 7 or 10 - 12, wherein at least one of A1, A2 & A3 is derived from a phosphoric acid ester.
19. A catalyst as claimed in any one claims 1 - 7 or 10 - 12, wherein at least one of A1 , A2 & A3 is derived from a sulphonic acid or ester thereof.
20. A catalyst as claimed in claim 1 comprising a compound selected from Zr(DEAA)2(2- ethylhexoxide)2, Zr(n-butoxide)2(DEAA)2, Zr(n-propoxide)2(DEAA)2, Zr(DEAA)2(tert- amylalkoxide)2, Zr(DEAA)4 , Zr(t-butoxide)2(DEAA)2, Zr(DEAA)2(propanedioxide)2, Zr(DEAA)2(diethyleneglycoxide)2, Zr(DEAA)2(ethylacetoacetato)2,Zr(DEAA)2(2,4- pentanedionato)2,Zr(DEAA)2(diethylmalonate)2 Zr(DEAA)2(1 ,3-propanediol) Zr(DEAA)2(1 ,4- butanediol) and Zr(DEAA)2(diethyleneglycol); where DEAA represents a ligand derived from N.N-diethylacetoacetamide.
21. A catalyst as claimed in any one of claims 1 - 20 further comprising a solvent.
22. A catalyst as claimed in claim 21 , wherein said solvent comprises an alcohol, a polyol, a ketoamide, ethylacetoacetate, acetylacetone, diethylmalonate or an excess of a compound used to form one of the A ligands.
23. A catalyst as claimed in claim 21 or 22, comprising from 1 to 10 moles of solvent per mole of zirconium.
24. A catalyst as claimed in any one of the preceding claims, wherein the catalyst does not comprise a compound of bismuth as a co-catalyst.
25. A composition comprising at least one of (i) a polyisocyanate and
(ii) a polyol and a catalyst as claimed in any one of claims 1 - 24.
26. A composition as claimed in claim 25 wherein said catalyst comprises a compound selected from Zr(DEAA)2(2-ethylhexoxide)2, Zr(isopropoxide)2(DEAA)2, Zr(n-butoxide)2(DEAA)2, Zr(n- propoxide)2(DEAA)2, Zr(DEAA)2(tert-amylalkoxide)2, Zr(DEAA)4 , Zr(t-butoxide)2(DEAA)2, Zr(DEAA)2(propanedioxide)2, Zr(DEAA)2(diethyleneglycoxide)2,
Zr(DEAA)2(ethylacetoacetato)2,Zr(DEAA)2(2,4-pentanedionato)2,Zr(DEAA)2(diethylmalonate)2 Zr(DEAA)2(1 ,3-propanediol) Zr(DEAA)2(1 ,4-butanediol) and Zr(DEAA)2(diethyleneglycol); where DEAA represents a ligand derived from N,N-diethylacetoacetamide.
27. A composition as claimed in claim 25 or 26 further comprising one or more compounds selected from the list consisting of a release agent, filler, colourant, cross-linker, chain extender, blowing agent, fungicide, wax, impact modifier, surfactant, plasticiser, water, coupling agent, fire retardants.
28. A composition as claimed in any one of claims 25 - 27, wherein the composition does not comprise a compound of bismuth as a co-catalyst.
29. A process for the manufacture of a polyurethane comprising reacting a polyisocyanate compound with a compound containing an active hydrogen in the presence of a catalyst as claimed in any one of claims 1 - 24.
30. A process as claimed in claim 29, wherein said compound containing an active hydrogen comprises a hydroxyl-containing compound.
31. A process as claimed in claim 30, wherein said hydroxyl-containing compound comprises a polyol.
32. A process as claimed in claim 30, wherein said hydroxyl-containing compound comprises a lignocellulosic material.
33. A process as claimed in any one of claims 29 - 32, wherein said catalyst is selected from Zr(DEAA)2(2-ethylhexoxide)2, Zr(isopropoxide)2(DEAA)2, Zr(n-butoxide)2(DEAA)2, Zr(n- propoxide)2(DEAA)2, Zr(DEAA)2(tert-amylalkoxide)2, Zr(DEAA)4 , Zr(t-butoxide)2(DEAA)2, Zr(DEAA)2(propanedioxide)2, Zr(DEAA)2(diethyleneglycoxide)2,
Zr(DEAA)2(ethylacetoacetato)2,Zr(DEAA)2(2,4-pentanedionato)2,Zr(DEAA)2(diethylmalonate)2 Zr(DEAA)2(1 ,3-propanediol) Zr(DEAA)2(1 ,4-butanediol) and Zr(DEAA)2(diethyleneglycol); where DEAA represents a ligand derived from N,N-diethylacetoacetamide.
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