Tailored SiOC-based polyethersiloxanes

Patent metadata

Field	Value
Publication number	US-11261298-B2
Application number	US-202015929842-A
Country	US
Kind code	B2
Filing date	May 26, 2020
Priority date	May 28, 2019
Publication date	Mar 1, 2022
Grant date	Mar 1, 2022

Abstract

SiOC-based polyethersiloxanes are prepared based on linear α,ω-hydroxy group-bearing siloxanes. In a first step, α,ω-acetoxy group-bearing linear polysiloxanes are prepared. In a second step, the α,ω-acetoxy group-bearing linear polysiloxanes are converted into the desired organosiloxane units, preferably shorter organosiloxane units, wherein the thus converted organosiloxane units have α,ω-acetoxy groups. In a third step, the α,ω-acetoxy group-bearing linear polysiloxanes from step 2 react with polyetherols to give SiOC-based polyethersiloxanes.

First claim

The invention claimed is:

1. A process for preparing a SiOC-based polyethersiloxane based on a linear α,ω-hydroxy group-bearing siloxane, the process comprising:
in a first step, preparing an α,ω-acetoxy group-bearing linear polysiloxane from the linear α,ω-hydroxy group-bearing siloxane,
in a second step, converting the α,ω-acetoxy group-bearing linear polysiloxane with a desired number of organosiloxane units, wherein the converted α,ω-acetoxy group-bearing linear polysiloxane have α,ω-acetoxy groups, and
in a third step, reacting the converted α,ω-acetoxy group-bearing linear polysiloxane from the second step with a polyetherol and optionally monool to give a SiOC-based polyethersiloxane.

2. The process according to claim 1 , comprising
in the first step, reacting the linear α,ω-hydroxy group-bearing polysiloxane with acetic anhydride to give an acetoxy group-bearing linear polysiloxane, and
in the second step, equilibrating the acetoxy group-bearing linear polysiloxane from the first step with a mixture, comprising acetic anhydride and an acid, in order to obtain the α,ω-acetoxy group-bearing linear polysiloxane with the desired number of organosiloxane units.

3. The process according to claim 2 , wherein the linear α,ω-hydroxy group-bearing siloxane satisfies at least formula (I):

wherein R 1 is an alkyl radical and/or aromatic radical, comprising 1 to 10 carbon atoms, and
wherein 1≤n≤19,000.

4. The process according to claim 2 , wherein the acid is a superacid having a pKa of less than −3.0.

5. The process according to claim 2 , wherein in the third step, the converted α,ω-acetoxy group-bearing polysiloxane from the second step is reacted with the polyetherol and optionally the monool.

6. The process according to claim 5 , wherein the monool employed is selected from the group consisting of ethanol, propanol, isopropanol, butanol, isobutanol, and a polyetherol of formula
A[—O—(CH 2 —CHR′—O—) m —(CH 2 —CH 2 —O—) n —(CH 2 —CH(CH 3 )—O—) o —Z] a

wherein
A is a saturated or unsaturated organic radical comprising at least one carbon atom
R′ is independently a saturated alkyl group comprising 2-18 carbon atoms or an aromatic radical,
Z is hydrogen,
m equals from 0 to 50,
n equals from 0 to 250,
equals from 0 to 250, and
a equals 1.

7. The process according to claim 2 , wherein in the third step a replacement of siloxane-bonded acetoxy groups occurs in the presence of a base.

8. The process according to claim 2 , wherein in the third step a replacement of siloxane-bonded acetoxy groups via reaction with the polyetherol is effected using an inert solvent, and optionally already present, acetic acid.

9. The process according to claim 2 , wherein in the third step a replacement of the siloxane-bonded acetoxy groups via the reaction with the polyetherol occurs without solvent.

10. The process according to claim 1 , wherein the α,ω-acetoxy group-bearing linear polysiloxane converted in the second step has 5-50 organosiloxane units.

11. The process according to claim 1 , wherein in the second step, a silane bearing alkoxy groups is additionally added in order to obtain a branched α,ω-acetoxy group-bearing polysiloxane.

12. The process according to claim 11 , wherein at least 1 mole of polyether-bonded OH functionality is used per mole of acetoxy group of the branched α,ω-acetoxy group-bearing polysiloxane.

13. The process according to claim 1 , wherein acetic acid is added in the second step.

14. The process according to claim 1 , wherein the polyetherol is of formula (II):
A[—O—(CH 2 —CHR′—O—) m —(CH 2 —CH 2 —O—) n —(CH 2 —CH(CH 3 )—O—) o —Z] a   (II)

wherein
A is either hydrogen or a saturated or unsaturated organic radical comprising at least one carbon atom,
R′ is independently a saturated alkyl group comprising 2-18 carbon atoms or an aromatic radical,
Z is hydrogen,
m equals from 0 to 50,
n equals from 0 to 250,
equals from 0 to 250,
a equals from 1 to 8, and
with the proviso that a sum of m, n, and o is equal to or greater than 1 and with the proviso that at least one of A or Z represents hydrogen.

15. The process according to claim 1 ,
wherein the second step comprises transesterification of the α,ω-acetoxy group-bearing linear polysiloxane,
wherein the transesterification is conducted in a solvent which is inert under reaction conditions,
wherein a total water content of the solvent is ≤50 ppm by mass, and
wherein determination of the total water content is performed by Karl Fischer titration.

16. The process according to claim 15 , wherein the transesterification is conducted in a temperature range from 40° C. to 180° C.

17. The process according to claim 15 , wherein the transesterification is conducted at reduced pressure and/or while passing through an inert gas.

18. A preparation produced by the process of claim 1 , comprising:
at least one SiOC-linked, branched silicone polyether,
the polyetherol, and
a polyether endcapped with an acetyl group,
with the proviso that a polyether radical present in the at least one SiOC-linked, branched silicone polyether is chemically identical to a polyether radical of the polyetherol and to a polyether radical of the polyether endcapped with an acetyl group, and
wherein a proportion of the SiOC-linked, branched silicone polyether is at least 50 percent by mass based on the preparation.

19. A method, comprising:
producing at least one product selected from the group consisting of defoamers, deaerating agents, foam stabilizers, wetting agents, paint and levelling additives, and demulsifiers, with the preparation according to claim 18 .

20. A method, comprising:
producing at least one product selected from the group consisting of diesel defoamers, hydrophobizing agents, polymer dispersions, adhesives, sealants, paper towels, cleaning and care formulations for household or for industrial applications, cosmetic, pharmaceutical, or dermatological compositions, construction material compositions, and thermoplastic shaped bodies, with the preparation according to claim 18 .

21. The preparation according to claim 18 , wherein the preparation is selected from the group consisting of:
a processing aid in an extrusion of thermoplastics,
an adjuvant in crop protection,
an additive for cleaning and caring of hard surfaces,
a surface treatment of fibres, particles, or fabrics, and
a coating of fillers.

Assignees

• Evonik Operations Gmbh

Inventors

• Favresse Philippe
• Fiedel Michael
• Brötzmann André
• Knott Wilfried
• Dudzik Horst

Classifications

• C08L83/12

  containing polyether sequences · CPC title

• C08G77/14

  containing silicon bound to oxygen-containing groups · CPC title

• C08L2205/03

  containing three or more polymers in a blend · CPC title

• C08G77/16

  to hydroxy groups · CPC title

• C08G77/46 Primary

  containing polyether sequences · CPC title