Process for preparing metal cyanide complex catalyst
AssigneeArco Chemical Technology, L.P.
InventorsHarry R. Hinney, Don S. Wardius
Life of this patent
Estimating the term…
Abstract
Highly active double metal cyanide complex catalysts suitable for use in ring-opening polymerization reactions may be prepared in filterable form by controlling the order of reagent addition, the temperature of the reaction medium, and the stoichiometric ratio of the reactants.
Claims20
A method of preparing a metal cyanide complex catalyst comprising the steps of:
- (a) adding a first aqueous solution of a water-soluble metal salt having the formula M.sup.1 (X).sub.n, wherein M.sup.1 is selected from the group consisting of Zn(II), Fe(II), Co(III), Ni(II), Mn(II), Co(II), Sn(II), Pb(II), Fe(III), Mo(IV), Mo(VI), Al(III), V(IV), V(V), Sr(II), W(IV), W(VI), Cu(II), and Cr(III);
- X is a first anion selected from the group consisting of halide, hydroxide, sulphate, carbonate, cyanate, thiocyanate, isocyanate, isothiocyanate, carboxylate, oxalate, or nitrate;
- and n is an integer satisfying the valency state of M.sup.1, to a second aqueous solution of a water-soluble metal cyanide salt having the formula (Y).sub.a M.sup.2 (CN).sub.b (A).sub.c, wherein M.sup.2 is the same as or different from M.sup.1 and is selected from the group consisting of Fe(II), Fe(III) Co(III), Cr(III), Mn(II), Mn(III), Ir(III), Rh(III), Ru(II), V(IV), V(V), Co(II), and Cr(II);
- Y is an alkali metal or alkaline earth, A is a second anion that may be the same as or different from X and is selected from the group consisting of halide, hydroxide, sulphate, carbonate, cyanate, thiocyanate, isocyanate, isothiocyanate, carboxylate, oxalate, or nitrate;
- a and b are each integers of 1 or greater;
- and a, b, and c are selected so as to provide the overall electroneutrality of the water-soluble metal cyanide salt, wherein the stoichiometric excess of the water soluble metal salt relative to water soluble metal cyanide salt is at least about 100%, the temperature of the second aqueous solution during the addition is from about 30.degree. C. to 75.degree. C., and wherein either or both of the first and second aqueous solutions optionally contain a first water miscible heteroatom-containing organic ligand selected from the group consisting of alcohols, aldehydes, ketones, ethers, esters, ureas, amides, nitriles, or sulfides, to form an aqueous slurry of particulate metal cyanide complex catalyst produced by reaction of the water-soluble metal salt and the water-soluble metal cyanide salt;
- (b) combining the aqueous slurry with a second water-miscible heteroatom-containing organic ligand, which may be the same as or different from the first organic ligand and is selected from the group consisting of alcohols, aldehydes, ketones, ethers, esters, amides, ureas, nitriles, or sulphides, said combining step being optional unless neither the first nor the second aqueous solution contained any water-miscible heteroatom-containing organic ligand;
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- (c) recovering the particulate metal cyanide complex catalyst from the aqueous slurry by filtration.
The method of claim wherein Y is selected from the group consisting of Li, Na, K, and Ca.
A method of preparing a metal cyanide complex catalyst comprising the steps of:
- (a) adding a first aqueous solution of a water-soluble zinc (II) salt having the formula Zn(X).sub.n, wherein X is a first anion selected from the group consisting of fluoride, chloride, bromide, iodide, sulphate, nitrate, acetyl acetonate, and acetate, and n is an integer satisfying the valency state of the Zn, to a second aqueous solution of a water-soluble metal cyanide salt having the formula (Y).sub.a M.sup.2 (CN).sub.b, wherein M.sup.2 is selected from the group consisting of Fe(II), Fe(III), Co(III), Ir(III), Ni(II), and Co(II), Y is selected from the group consisting of Li, Na, K, and Ca, and b is an integer of at least 1 selected so as to provide the overall electroneutrality of the water-soluble metal cyanide salt, wherein the stoichiometric excess of the water-soluble metal salt relative to the water soluble metal cyanide salt is at least about 150%, the temperature of the second aqueous solution during the addition is from about 30.degree. C. to 60.degree. C., and wherein either or both the first and second aqueous solutions optionally contain a first water-miscible heteroatom-containing organic ligand selected from the group consisting of ethers and ketones, to form an aqueous slurry of particulate metal cyanide complex catalyst produced by reaction of the water-soluble metal salt and the water-soluble metal cyanide salt;
- (b) combining the aqueous slurry with a second water-miscible heteroatom-containing organic ligand, which may be the same as or different from the first organic ligand and is selected from the group consisting of ethers and ketones, said combining step being optional unless neither the first nor second aqueous solutions contain any water-miscible heteroatom-containing organic ligand;
- (c) recovering the particulate metal cyanide complex catalyst from the aqueous slurry by filtration;
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- (d) washing the recovered particulate metal cyanide complex catalyst with at least one portion of a washing liquid selected from the group consisting of water-miscible heteroatom-containing organic ligands, water, and mixtures thereof.
A method of preparing a metal cyanide complex catalyst comprising the steps of:
- (a) adding a first aqueous solution of zinc chloride to a second aqueous solution of potassium hexacyanocobaltate over a period of from about 10 minutes to 10 hours, wherein the molar ratio of zinc chloride:potassium hexacyanocobaltate is at least about 3.75:1 and the temperature of the second aqueous solution during the addition is from about 30.degree. C. to 60.degree. C., to form an aqueous slurry of particulate metal cyanide complex catalyst produced by reaction of the zinc chloride and potassium hexacyanocobaltate;
- (b) combining the aqueous slurry with at least one organic ligand selected from the group consisting of glyme, diglyme, triglyme, dioxane, tetrahydrofuran, acetone, 1,3-dimethoxypropane, diethoxyethane, propylene glycol dimethyl ether, 1,1,3,3-tetramethylurea, 2,5-hexanedione, and acetylacetone, wherein the molar ratio of organic ligand:potassium hexacyanocobaltate is not greater than about 50:1;
- (c) recovering the particulate metal cyanide complex catalyst from the aqueous slurry by filtration;
- (d) washing the recovered particulate metal cyanide complex catalyst with at least one additional portion of the organic ligand so as to substantially remove the excess water from the recovered particulate metal cyanide complex catalyst;
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- (e) drying the washed particulate metal cyanide catalyst.
Dependencies are inferred from the claim text.