Method for producing polyetherester carbonate polyols

Patent metadata

Field	Value
Publication number	US-9296859-B2
Application number	US-201214365622-A
Country	US
Kind code	B2
Filing date	Dec 10, 2012
Priority date	Dec 16, 2011
Publication date	Mar 29, 2016
Grant date	Mar 29, 2016

Abstract

The present invention relates to a method for producing polyetherester carbonate polyols by means of catalytic addition of carbon dioxide, alkylene oxides and cyclic anhydrides to H-functional starter compounds in the presence of double metal cyanide (DMC) catalysts.

First claim

The invention claimed is:

1. A process for preparing a polyether ester carbonate polyol comprising
conducting catalytic addition of carbon dioxide, with one or more alkylene oxides and one or more cyclic anhydrides onto one or more H-functional starter substances in the presence of a double metal cyanide (DMC) catalyst,
wherein, in a first step (α), the DMC catalyst and the one or more H-functional starter substances are initially charged and, in a second step (β), the DMC catalyst is activated by addition of the one or more alkylene oxides and CO 2 and optionally one or more cyclic anhydrides,
wherein, in the second step (β), a portion (based on the total amount of alkylene oxides used in steps (β) and (γ)) of the one or more alkylene oxides and optionally a portion (based on the total amount of cyclic anhydrides used in steps (β) and (γ) of the one or more cyclic anhydrides is added to a mixture resulting from step (α),
wherein addition of the portion of the one or more alkylene oxides can be effected in the presence of CO 2 and/or inert gas, and
wherein the second step (β) can also be effected more than once, and,
in a third step (γ), which is in a polymerization stage, the one or more alkylene oxides, the one or more cyclic anhydrides, and a CO 2 monomer are metered constantly into a mixture resulting from the second step (β).

2. The process as claimed in claim 1 , wherein, in (α),
(α1) a reactor is initially charged with the DMC catalyst and one or more H-functional starter compounds,
(α2) 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 (in absolute terms) of 10 mbar to 800 mbar is established in the reactor by removing the inert gas or carbon dioxide to conduct a first activation stage.

3. The process as claimed in claim 2 , wherein the double metal cyanide catalyst is added to the H-functional starter substance and/or a mixture of at least two H-functional starter substances in (α1) and/or immediately thereafter in (α2).

4. The process as claimed in claim 1 , wherein, in (γ), the carbon dioxide is introduced into the mixture by
(i) sparging a reaction mixture in the reactor from below,
(ii) using a hollow-shaft stirrer,
(iii) combination of metering methods set forth in said (i) and (ii), and/or
(iv) sparging via a liquid surface by use of one or more multilevel stirrer units.

5. The process as claimed in claim 1 , wherein, in steps (β) and/or (γ), the carbon dioxide is introduced into the mixture by sparging the reaction mixture in the reactor from below using an inlet tube, using a sparging ring and/or using a combination of inlet tube and/or sparging ring with a gas-distributing stirrer.

6. The process as claimed in claim 1 , wherein the polymerization stage (γ) is conducted in a stirred tank, tubular reactor and/or loop reactor.

7. The process as claimed in claim 1 , wherein the cyclic anhydride used is at least one compound of the formula (II), (III) or (IV)

where
R1 and R2 are each hydrogen, halogen, C1-C22-alkyl, C1-C22-alkenyl or C6-C18-aryl, or R1 and R2 are members of a 4- to 7-membered ring or polycyclic system,
R3, R4, R5 and R6 are each hydrogen, C1-C22-alkyl, C1-C22-alkenyl or C6-C18-aryl or are members of a 4- to 7-membered ring or polycyclic system and
R7, R8, R9, R10, R11 and R12 are each hydrogen, C1-C22-alkyl, C1-C22-alkenyl or C6-C18-aryl or are members of a 4- to 7-membered ring or polycyclic system.

8. The process as claimed in claim 1 , wherein the cyclic anhydride used is at least one compound selected from the group consisting of maleic anhydride, phthalic anhydride, 1,2-cyclohexanedicarboxylic anhydride, diphenic anhydride, tetrahydrophthalic anhydride, methyltetrahydrophthalic anhydride, norbornenedioic anhydride and chlorination products thereof, succinic anhydride, glutaric anhydride, diglycolic anhydride, 1,8-naphthalic anhydride, succinic anhydride, dodecenylsuccinic anhydride, tetradecenylsuccinic anhydride, hexadecenylsuccinic anhydride, octadecenylsuccinic anhydride, 3- and 4-nitrophthalic anhydride, tetrachlorophthalic anhydride, tetrabromophthalic anhydride, itaconic anhydride, dimethylmaleic anhydride and allylnorbornenedioic anhydride.

9. The process as claimed in claim 1 , wherein the one or more H-functional starter substances used are selected from at least one of the group consisting of alcohols, amines, thiols, amino alcohols, thio alcohols, hydroxy esters, polyether polyols, polyester polyols, polyester ether polyols, polycarbonate polyols, polyether carbonate polyols, polyethyleneimines, polyetheramines, polytetrahydrofurans, polyether thiols, polyacrylate polyols, castor oil, the mono- or diglyceride of castor oil, monoglycerides of fatty acids, chemically modified mono-, di- and/or triglycerides of fatty acids and C 1 - 24 -alkyl fatty acid esters containing an average of at least 2 OH groups per molecule.

10. The process as claimed in claim 1 , wherein the one or more H-functional starter substances used 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, di- and trifunctional polyether polyols, where the polyether polyol has been formed from 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 have a molecular weight M n in a range from 62 to 4500 g/mol and a functionality of 2 to 3.

11. The process as claimed in claim 1 , wherein the double metal cyanide catalyst used comprises at least one double cyanide compound selected from the group consisting of zinc hexacyanocobaltate(III), zinc hexacyanoiridate(III), zinc hexacyanoferrate(III) and cobalt(II) hexacyanocobaltate(III).

12. The process as claimed in claim 1 , wherein the double metal cyanide catalyst comprises at least one unsaturated alcohol as an organic complex ligand.

13. The process as claimed in claim 1 , wherein the double metal cyanide catalyst used comprises at least one organic complex 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-oxetanemethanol.

14. The process as claimed in claim 1 , wherein DMC catalyst is activated by addition of alkylene oxide, CO 2 and one or more cyclic anhydrides.

15. The process as claimed in claim 1 , wherein the polymerization stage (γ) is conducted at a temperature of 60 to 150° C.

16. The process as claimed in claim 1 , wherein the alkylene oxide used is one or more compounds selected from the group consisting of ethylene oxide, propylene oxide, 1-butene oxide, 2,3-butene oxide, 2-methyl-1,2-propene oxide (isobutene oxide), 1-pentene oxide, 2,3-pentene oxide, 2-methyl-1,2-butene oxide, 3-methyl-1,2-butene oxide, 1-hexene oxide, 2,3-hexene oxide, 3,4-hexene oxide, 2-methyl-1,2-pentene oxide, 4-methyl-1,2-pentene oxide, 2-ethyl-1,2-butene oxide, 1-heptene oxide, 1-octene oxide, 1-nonene oxide, 1-decene oxide, 1-undecene oxide, 1-dodecene oxide, 4-methyl-1,2-pentene oxide, butadiene monoxide, i

Assignees

• Bayer Ip Gmbh

Inventors

• Guertler Christoph
• Mueller Thoams Ernst
• Kermagoret Anthony
• Dienes Yvonne
• Barruet Julien
• Wolf Aurel
• Grasser Stefan

Classifications

• C08G64/34

  and cyclic ethers · CPC title

• C08G65/2615

  the other compounds containing carboxylic acid, ester or anhydride groups · CPC title

• C08G65/2663 Primary

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

• C08G64/183

  containing polyether sequences · CPC title

• C08G65/26

  from cyclic ethers and other compounds · CPC title