Aminosiloxanes of high purity

Patent metadata

Field	Value
Publication number	US-9951185-B2
Application number	US-201514978804-A
Country	US
Kind code	B2
Filing date	Dec 22, 2015
Priority date	Dec 23, 2014
Publication date	Apr 24, 2018
Grant date	Apr 24, 2018

Abstract

Disclosed herein is a composition comprising amino-functional polysiloxanes of high purity and their preparation. Also disclosed herein is an aminoalkyl-functional polysiloxane, a process for purifying this aminoalkyl-functional polysiloxane, a process for preparing the composition, a use of the composition, a polyorganosiloxane-polyorgano block copolymer, a process for the preparation of a polyorganosiloxane-polyorgano block copolymer and a shaped, formed and/or extruded shaped article.

First claim

What is claimed is:

1. A composition having a Hazen number of from 0 to 100 and a H 2 N-functionality of from 1.96 to less than 2.00 comprising:
(A) at least one aminoalkyl-functional polysiloxane of general formula (I):

wherein
R 1 is independently selected from the group consisting of a monovalent linear alkyl, branched alkyl, arylalkyl, alkylaryl, and aryl groups containing up to 20 carbon atoms,
each R 2 is independently a linear or branched divalent C3 or C4 alkyl group, and
n is an integer of from 0 to 7; and
(B) at least one compound comprising at least one iminoalkyl functional group obtained from the hydrosilylation of at least one olefinic amine and at least one hydridosiloxane in the presence of a platinum catalyst,

wherein the H 2 N-functionality is determined by 1 H NMR using the equation:
[H 2 N−functionity=2.0*(1−[mol % impurity−CH]/100,

wherein the mole percent impurity-CH functionality is calculated from the corresponding area integral of the impurity (N═CH)-signals of the iminoalkyl groups, observed in the range of from 7.4 to 7.7 ppm versus the integrals of the SiCH n′ , where n′ is 1 or 2 observed in the range of from 0.4 to 0.7 ppm, and wherein the composition is made by a process comprising the steps of:
(i) reacting a composition having an H 2 N-functionality of greater than 0 and less than 1.96 and/or color according to Hazen number of greater than 100 comprising at least one an aminoalkyl-functional polysiloxane and at least one compound comprising at least one iminoalkyl functional group with a stoichiometric excess, related to the content of H 2 N-groups, of an acid with a pKa less than or equal to 5.5 and a stoichiometric excess of water, related to the acid, to provide for a reaction product composition,
(ii) removing the volatile compounds present in the reaction product composition of step (i) by distillation, optionally with the use of an inert carrier gas, at a temperature of from 40° C. to 250° C. and at a pressure of from 0.1 mbar to 1030 mbar to provide for a devolatilized higher boiling composition,
(iii) neutralizing the resulting devolatilized higher boiling composition of step (ii) with at least one base to provide for a neutralized and devolatilized higher boiling composition, and
(iv) depolymerizing the neutralized and devolatilized higher boiling composition of step (iii) in the presence of at least one base to produce a composition containing at least one amino-functional polysiloxane of formula (I), and
(v) distilling the composition containing at least one amino-functional polysiloxane of step (iv) at a temperature of from 60° C. to 250° C. and at a pressure of from 0.1 mbar to 1030 mbar to provide for the composition comprising components (A) and (B) and having a Hazen number of from 0 to 100 and a H 2 N-functionality of from 1.96 to less than 2.00.

2. The composition having a Hazen number of from 0 to 100 and a H 2 N-functionality of from 1.96 to less than 2.00 according to claim 1 , wherein the at least one acid of reaction step (i) is hydrochloric acid.

3. The composition having a Hazen number of from 0 to 100 and a H 2 N-functionality of from 1.96 to less than 2.00 according to claim 1 , wherein the base catalyst in step (iv) is sodium hydroxide, potassium hydroxide, cesium hydroxide or their related silanolates.

4. The composition having a Hazen number of from 0 to 100 and a H 2 N-functionality of from 1.96 to less than 2.00 according to claim 1 , wherein the R 1 groups are monovalent methyl or phenyl groups.

5. The composition having a Hazen number of from 0 to 100 and a H 2 N-functionality of from 1.96 to less than 2.00 according to claim 1 , wherein the R 2 groups are —CH 2 CH 2 CH 2 — or —CH(CH 3 )CH 2 —.

6. The composition having a Hazen number of from 0 to 100 and a H 2 N-functionality of from 1.96 to less than 2.00 according to claim 1 , wherein in process step (i) the aminoalkyl-functional polysiloxane has a color according to Hazen in the range of greater than 100 to 500.

7. The composition having a Hazen number of from 0 to 100 and a H 2 N-functionality of from 1.96 to less than 2.00 according to claim 1 , wherein in process step (i), wherein the excess of water to acid is in a range of from 3 moles of water to acid to 10 moles of water to acid.

8. The composition having a Hazen number of from 0 to 100 and a H 2 N-functionality of from 1.96 to less than 2.00 according to claim 1 , wherein in process step (i), the reaction temperature is controlled between 10-30 degrees Celsius.

9. The composition having a Hazen number of from 0 to 100 and a H 2 N-functionality of from 1.96 to less than 2.00 according to claim 1 , wherein in process step (iv) the base used is the base from step (iii).

Assignees

• Momentive Performance Mat Gmbh
• Momentive Performance Mat Inc

Inventors

• Huggins John M
• Eversheim Hurbertus
• Hoffmüller Gunnar

Classifications

• C08G77/06 Primary

  Preparatory processes · CPC title

• C08G77/458

  containing polyurethane sequences · CPC title

• C08G77/26 Primary

  nitrogen-containing groups · CPC title

• C08G77/34

  Purification · CPC title

• C08G77/38

  Polysiloxanes modified by chemical after-treatment · CPC title