Alkylene oxide polymerization using a double metal cyanide catalyst complex and a magnesium, group 3-group 15 metal or lanthanide series metal compound

Patent metadata

Field	Value
Publication number	US-10233284-B2
Application number	US-201615382519-A
Country	US
Kind code	B2
Filing date	Dec 16, 2016
Priority date	Dec 27, 2010
Publication date	Mar 19, 2019
Grant date	Mar 19, 2019

Abstract

Alkylene oxide polymerizations are performed in the presence of a double metal cyanide polymerization catalyst and certain magnesium, Group 3-Group 15 metal or lanthanide series metal compounds. The presence of the magnesium, Group 3-Group 15 metal or lanthanide series metal compound provides several benefits including more rapid catalyst activation, faster polymerization rates and the reduction in the amount of ultra high molecular weight polymers that are formed. The catalyst mixture is unexpectedly useful in making polyethers having low equivalent weights.

First claim

What is claimed is:

1. A method for producing a polyether monol or polyether polyol product, comprising polymerizing at least one alkylene oxide in the presence of a double metal cyanide catalyst complex and at least one magnesium, gallium or indium compound not present during the preparation of the double metal cyanide catalyst complex in which magnesium, gallium or indium is bonded to at least one alkoxide, aryloxy, carboxylate, acyl, pyrophosphate, phosphate, thiophosphate, dithiophosphate, phosphate ester, thiophosphate ester, amide, siloxide, hydride, carbamate or hydrocarbon anion, and wherein the magnesium, gallium or indium compound is devoid of halide anions.

2. The method of claim 1 which includes the steps of:
combining (a) the double metal cyanide catalyst complex (b) the magnesium, gallium or indium compound, (c) at least one initiator compound, and (d) at least one alkylene oxide to form a starting reaction mixture,
heating the starting reaction mixture to polymerization conditions until the double metal cyanide catalyst complex becomes activated, and then
feeding additional alkylene oxide to the reaction mixture under polymerization conditions.

3. The method of claim 1 which includes the steps of:
establishing steady-state concentrations of 1) the DMC catalyst, 2) the magnesium, gallium or indium compound, 3) at least one initiator, 4) at least one alkylene oxide and 5) polymerizate in a continuous reactor under polymerization conditions,
continuously adding additional initiator, alkylene oxide, DMC catalyst complex, additional magnesium, gallium or indium compound, or a catalyst mixture formed by combining the DMC catalyst complex and magnesium, gallium or indium compound, to the continuous reactor under polymerization conditions and continuously withdrawing a product stream containing polyether monol or polyether polyol product from the continuous reactor.

4. A method for preparing an alkylene oxide polymerization catalyst mixture, comprising combining (a) a double metal cyanide catalyst complex and (b) at least one magnesium, gallium or indium compound not present during the preparation of the double metal cyanide catalyst complex in which magnesium, gallium or indium is bonded to at least one alkoxide, aryloxy, carboxylate, acyl, pyrophosphate, phosphate, thiophosphate, dithiophosp hate, phosphate ester, thiophosp hate ester, amide, siloxide, hydride, carbamate or hydrocarbon anion, and wherein the magnesium, gallium or indium compound is devoid of halide anions to form a catalyst mixture and then performing a preliminary heating step by heating the catalyst mixture to a temperature of from 80 to 220° C. at atmospheric or subatmospheric pressure for a period of 10 minutes or more prior to combining the catalyst mixture with an alkylene oxide.

5. The method of claim 1 , wherein the magnesium, gallium or indium compound is one or more of a trialkyl gallium compound; a gallium alkoxide; a gallium aryloxide; a gallium carboxylate, a gallium amide; gallium acetylacetonate; gallium t-butylacetylacetonate; an alkylgallium alkoxide; a trialkyl indium compound; an indium aryloxide; an indium carboxylate; indium acetylacetonate; and indium t-butylacetylacetonate.

6. The method of claim 1 , wherein the magnesium, gallium or indium compound is one or more of trimethylgallium, triethyl gallium, tributyl gallium, tribenzylgallium, trimethoxide, gallium triethoxide, gallium triisopropoxide, gallium tri-t-butoxide, gallium tri-sec-butoxide, gallium phenoxide, a gallium phenoxide in which one or more of the phenoxide groups is ring-substituted with alkyl, CF 3 , cyano, COCH 3 , halogen, hydroxyl or alkoxyl, gallium formate, gallium acetate, gallium propionate, gallium 2-ethylhexanoate, gallium benzoate, a gallium benzoats in which one or more of the benzoate groups is ring-substituted with alkyl, CF 3 , cyano, COCH 3 , halogen, hydroxyl or alkoxyl, gallium salicylate, gallium 3,5-di-t-butyl salicylate; gallium tris(dimethylamide), gallium tris(diethylamide), gallium tris(dip henylamide), gallium tris(di(trimethylsilyl)amide), gallium acetylacetonate, gallium t-butylacetylacetonate, diethylgallium ethoxide, dimethylgallium ethoxide, diethylgallium isopropoxide, dimethylgallium isopropoxide, trimethyl indium, indium methoxide, indium ethoxide, indium isopropoxide, indium t-butoxide, indium sec-butoxide, indium phenoxide, and indium phenoxide in which one or more of the phenoxide groups is ring-substituted with alkyl, CF 3 , cyano, COCH 3 , halogen, hydroxyl or alkoxyl; indium formate, indium acetate, indium propionate, indium 2-ethylhexanoate, indium benzoate, an indium benzoate in which one or more of the benzoate groups is ring-substituted with alkyl, CF 3 , cyano, COCH 3 , halogen, hydroxyl or alkoxyl, indium salicylate, indium 3,5-di-t-butyl salicylate, indium acetylacetonate and indium t-butylacetylacetonate.

7. The method of claim 1 wherein the magnesium, gallium or indium compound is a gallium or indium alkoxide, wherein at least one alkoxide group of the gallium or indium alkoxide is a residue, after removal of at least one hydroxyl hydrogen, of a polyether monol or polyether polyol.

8. The method of claim 4 , wherein the magnesium, gallium or indium compound is one or more of a trialkyl gallium compound; a gallium alkoxide; a gallium aryloxide; a gallium carboxylate, a gallium amide; gallium acetylacetonate; gallium t-butylacetylacetonate; an alkylgallium alkoxide; a trialkyl indium compound; an indium aryloxide; an indium carboxylate; indium acetylacetonate; and indium t-butylacetylacetonate.

9. The method of claim 4 , wherein the magnesium, gallium or indium compound is one or more of trimethylgallium, triethyl gallium, tributyl gallium, tribenzylgallium, trimethoxide, gallium triethoxide, gallium triisopropoxide, gallium tri-t-butoxide, gallium tri-sec-butoxide, gallium phenoxide, a gallium phenoxide in which one or more of the phenoxide groups is ring-substituted with alkyl, CF 3 , cyano, COCH 3 , halogen, hydroxyl or alkoxyl, gallium formate, gallium acetate, gallium propionate, gallium 2-ethylhexanoate, gallium benzoate, a gallium benzoats in which one or more of the benzoate groups is ring-substituted with alkyl, CF 3 , cyano, COCH 3 , halogen, hydroxyl or alkoxyl, gallium salicylate, gallium 3,5-di-t-butyl salicylate; gallium tris(dimethylamide), gallium tris(diethylamide), gallium tris(diphenylamide), gallium tris(di(trimethylsilyl)amide), gallium acetylacetonate, gallium t-butylacetylacetonate, diethylgallium ethoxide, dimethylgallium ethoxide, diethylgallium isopropoxide, dimethylgallium isopropoxide, trimethyl indium, indium methoxide, indium ethoxide, indium isopropoxide, indium t-butoxide, indium sec-butoxide, indium phenoxide, and indium phenoxide in which one or more of the phenoxide groups is ring-substituted with alkyl, CF 3 , cyano, COCH 3 , halogen, hydroxyl or alkoxyl; indium formate, indium acetate, indium propionate, indium 2-ethylhexanoate, indium benzoate, an indium benzoate in which one or more of the benzoate groups is ring-substituted with alkyl, CF 3 , cyano, COCH 3 , halogen, hydroxyl or alkoxyl, indium salicylate, indium 3,5-di-t-butyl salicylate, indium acetylacetonate and indium t-butylacetylacetonate.

10. The method of claim 1 , wherein the magnesium, gallium or indium compound is one or more of a magnesium alkyl, a magnesium alkoxide, a magnesium aryloxide, a magnesium carboxylate, a magnesium amide, a magnesium acetylacetonate and magnesium t-butylacetylacetonate.

11. The method of claim 1 , wherein the magnesium, gallium or indium compound is one or more of diethyl magnesium, dibutyl magnesium, butylethyl magnesium, dibenzyl magnesium, magnesium methoxide, magnesium eth

Assignees

• Dow Global Technologies Llc

Inventors

• Laitar David S
• Babb David A
• Villa Carlos M
• Keaton Richard
• Masy Jean-Paul

Classifications

• C07C41/01

  Preparation of ethers · CPC title

• C07C41/02

  from oxiranes · CPC title

• C08G65/2663 Primary

  Metal cyanide catalysts, i.e. DMC's · CPC title

• C08G65/269

  Mixed catalyst systems, i.e. containing more than one reactive component or catalysts formed in-situ · CPC title

• C08G65/34

  from hydroxy compounds or their metallic derivatives {(C08G65/26 takes precedence)} · CPC title