Method for activating double metal cyanide catalysts for producing polyether polyols

Patent metadata

Field	Value
Publication number	US-9249259-B2
Application number	US-201214232015-A
Country	US
Kind code	B2
Filing date	Jul 17, 2012
Priority date	Jul 18, 2011
Publication date	Feb 2, 2016
Grant date	Feb 2, 2016

Abstract

The present invention relates to a process for the activation of double metal cyanide (DMC) catalysts and to a process for the preparation of polyethercarbonate polyols from one or more H-functional starter compounds, one or more alkylene oxides and carbon dioxide in the presence of a double metal cyanide catalyst, characterized in that
(α) (α1) the DMC catalyst and one or more H-functional starter compounds are placed in a reactor,
(α2) an inert gas, an inert gas/carbon dioxide mixture or carbon dioxide is passed through the reactor at a temperature of 50 to 200° C. and at the same time a reduced pressure (absolute) of 10 mbar to 800 mbar is established in the reactor by removal of the inert gas or carbon dioxide,
(β) under an atmosphere of inert gas/carbon dioxide mixture or under a pure carbon dioxide atmosphere, alkylene oxide is added to the mixture from step (α) at temperatures of 50 to 200° C., and (γ) one or more alkylene oxides and carbon dioxide are metered into the mixture resulting from step (β).

First claim

The invention claimed is:

1. A process for the preparation of a polyethercarbonate polyol from one or more H-functional starter compounds, one or more alkylene oxides and carbon dioxide in the presence of a double metal cyanide (DMC) catalyst, comprising
(α) (α1) placing the DMC catalyst and one or more H-functional starter compounds in a reactor,
(α2) passing an inert gas, an inert gas/carbon dioxide mixture or carbon dioxide through the reactor at a temperature of 50 to 200° C. and at the same time establishing a reduced pressure (absolute) of 10 mbar to 800 mbar in the reactor by removal of the inert gas or carbon dioxide, to form a mixture,

(β) adding, under an atmosphere of inert gas/carbon dioxide mixture or under a carbon dioxide atmosphere, a fraction based on the total amount of alkylene oxides used in steps (β) and (γ), one or more alkylene oxides to the mixture from step (α) at temperatures of 50 to 200° C., and
(γ) metering one or more alkylene oxides and carbon dioxide into a mixture resulting from step (β).

2. The process according to claim 1 wherein the amount of one or more alkylene oxides in step (β) is 0.1 to 25.0 wt. % based on the amount of starter compound used in step (α).

3. A process for the activation of a DMC catalyst, comprising
(α) (α1) placing the DMC catalyst and one or more H-functional starter compounds in a reactor,
(α2) passing an inert gas, an inert gas/carbon dioxide mixture or carbon dioxide through the reactor at a temperature of 50 to 200° C. and at the same time estblishing a reduced pressure (absolute) of 10 mbar to 800 mbar in the reactor by removal of the inert gas or carbon dioxide, to form a mixture, and
(β) adding, under an atmosphere of inert gas/carbon dioxide mixture or under a pure carbon dioxide atmosphere, alkylene oxide to the mixture from step (α) at temperatures of 50 to 200° C.

4. The process according to claim 1 comprising, in step (α),
(α1) placing the one or more H-functional starter compounds or a mixture of at least two H-functional starter compounds in the reactor, and
(α2) passing an inert gas, an inert gas/carbon dioxide mixture or carbon dioxide into the resulting mixture of DMC catalyst and one or more H-functional starter compounds at a temperature of 50 to 200° C., and at the same time establishing a reduced pressure (absolute) of 10 mbar to 800 mbar by removal of the inert gas or carbon dioxide,
wherein the DMC catalyst is added to the one or more H-functional starter compounds or the mixture of at least two H-functional starter compounds in step (α1) or directly thereafter in step (α2).

5. The process according to claim 1 wherein the inert gas is argon and/or nitrogen.

6. The process according to claim 1 comprising, in steps (β) and/or (γ), introducing the carbon dioxide into the mixture by
(i) feeding gas into the reaction mixture from underneath the reactor;
(ii) using a hollow shaft agitator;
(iii) combining the metering operations according to (i) and (ii); and/or
(iv) feeding gas over the liquid surface using agitating elements.

7. The process according to claim 1 wherein, in steps (β) and/or (γ), the carbon dioxide is introduced into the mixture by feeding gas into the reaction mixture from underneath the reactor via an inlet tube, a gas dispersion ring or a combination of an inlet tube or gas dispersion ring with a gas dispersion agitator.

8. The process according to claim 7 wherein one or more agitator stages are arranged on an agitator shaft above the gas dispersion agitator.

9. The process according to claim 1 wherein, in steps (β) and/or (γ), the carbon dioxide is introduced into the mixture through a tubular agitator or a pitched-blade turbine with hollow blades.

10. The process according to claim 1 wherein the one or more H-functional starter compounds are selected from at least one of the group consisting of alcohols, amines, thiols, amino alcohols, thio alcohols, hydroxy esters, polyether polyols, polyester polyols, polyesterether polyols, polycarbonate polyols, polyethercarbonate polyols, poly-ethyleneimines, polyetheramines, polytetrahydrofurans, polyetherthiols, polyacrylate polyols, castor oil, ricinoleic acid mono- or diglyceride, fatty acid monoglycerides, chemically modified fatty acid mono-, di- and/or triglycerides, and fatty acid C 1 -C 24 -alkyl esters containing an average of at least 2 OH groups per molecule.

11. The process according to claim 1 wherein the one or more H-functional starter compounds are selected from at least one of the group consisting of ethylene glycol, propylene glycol, 1,3-propanediol, 1,3-butanediol, 1,4-butanediol, 1,5-pentanediol, 2-methylpropane-1,3-diol, neopentyl glycol, 1,6-hexanediol, 1,8-octanediol, diethylene glycol, dipropylene glycol, glycerol, trimethylolpropane, and di- and trifunctional polyether polyols, the polyether polyol being made up of a di- or tri-H-functional starter substance and propylene oxide or a di- or tri-H-functional starter substance, propylene oxide and ethylene oxide, and the polyether polyols having a molecular weight M n ranging from 62 to 4500 g/mol and a functionality of 2 to 3.

12. The process according to claim 1 wherein the DMC catalyst comprises at least one double cyanide compound selected from the group consisting of zinc hexacyano-cobaltate(III), zinc hexacyanoiridate(III), zinc hexacyanoferrate(III), and cobalt(II) hexa-cyanocobaltate(III).

13. The process according to claim 1 wherein the DMC catalyst comprises at least one organic complexing ligand selected from the group consisting of aliphatic ether, ethanol, isopropanol, n-butanol, isobutanol, sec-butanol, tert-butanol, 2-methyl-3-buten-2-ol, 2-methyl-3-butyn-2-ol, ethylene glycol mono-tert-butyl ether, diethylene glycol mono-tert-butyl ether, tripropylene glycol monomethyl ether, and 3-methyl-3-oxetane-methanol.

14. The process according to claim 1 , wherein the process is carried out in a tubular reactor, an agitated tank or a loop reactor.

15. The process according to claim 1 , wherein the process is carried out in an agitated tank, a tubular reactor or a loop reactor, and wherein, in step (γ), one or more H-functional starter compounds are metered continuously into the agitated tank during the reaction.

Assignees

• Müller Thomas Ernst
• Gürtler Christoph
• Wohak Matthias
• Hofmann Jörg
• Subhani Muhammad Afzal
• Cosemans Maurice
• Leitner Walter
• Bayer Ip Gmbh

Inventors

• Müller Thomas Ernst
• Gürtler Christoph
• Wohak Matthias
• Hofmann Jörg
• Subhani Muhammad Afzal
• Cosemans Maurice
• Leitner Walter

Classifications

• C08G64/34 Primary

  and cyclic ethers · CPC title

• C08G64/323 Primary

  and alcohols · CPC title

• C08G65/2603

  the other compounds containing oxygen · CPC title

• C08G65/2663

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