IP Library › Granted Patent US 10,407,541
Granted Patent B2
US 10,407,541 · App. 15/564,524 · Granted Sep 10, 2019

Block co-condensates of polysiloxanes and dihydroxydiphenylcycloalkane-based n (CO)polycarbonates

Inventors: Alexander Meyer (Düsseldorf, DE); Klaus Horn (Dormagen, DE)
Assignee: Covestro Deutschland AG
C08G64/186C08G77/448C08G81/00C08G81/027C08L83/10C08L69/00
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Quick Facts
Patent No.
US 10,407,541
App. No.
15/564,524
Granted
Sep 10, 2019
Kind
B2
Abstract

The present invention relates to block cocondensates of polysiloxanes and dihydroxydiarylcycloalkane-based (co)polycarbonates and also to a process for preparing such block cocondensates. The invention further relates to the use of these block cocondensates for producing mouldings and extrudates.

Claims (64)

1. A block cocondensate comprising

(A) 1-80 wt % of structural units of the general formula (1), based on the total weight of the block cocondensate,

 in which

R 1 and R 2 independently of one another are hydrogen, halogen, C 1 -C 8 alkyl, C 5 -C 6 cycloalkyl, phenyl or C 7 -C 12 aralkyl,

R 3 and R 4 for each X are individually selectable and independently of one another are hydrogen or C 1 -C 6 alkyl, and

n is an integer from 4 to 7,

X is carbon,

with the proviso that on at least one atom X R 3 and R 4 are C 1 -C 6 alkyl;

(B) siloxane blocks of the general formula (2)

 where

R 5 is H,

R 6 and R 7 are each methyl,

V is O,

W is a single bond,

Y is isopropylidene,

m is an average number of repeat units from 2 to 5,

o is an average number of repeat units from 10 to 100,

q is 0, and

p is 0 or 1; and the product of m times o is a number between 15 and 200, and

(C) homopolycarbonate blocks which contain no structural units of the formula (1) and have a number-average molecular weight M n of at least 2000 g/mol.

2. The block cocondensate according to claim 1 , wherein the homopolycarbonate blocks derive from a homopolycarbonate obtained by the melt transesterification process.

3. The block cocondensate according to claim 1 , wherein the homopolycarbonate blocks (C) are based on bisphenol A.

4. The block cocondensate according to claim 1 , comprising copolycarbonate blocks which contain the structural units of the general formula (1).

5. The block cocondensate according to claim 4 , wherein the copolycarbonate blocks further have structural units which derive from a diphenol of the formula (3)

in which

R 8 and R 9 independently of one another are H, C 1 -C 18 alkyl, C 1 -C 18 alkoxy, halogen or optionally substituted aryl or aralkyl, and

Z is a single bond, —CO—, —O—, C 1 to C 6 alkylene, C 2 to C 5 alkylidene, is a C 5 to C 6 cycloalkylidene radical which may be substituted one or more times by C 1 to C 4 alkyl, or is C 6 to C 12 arylene, which may be fused to a further aromatic ring containing heteroatoms.

6. The block cocondensate according to claim 4 , wherein the copolycarbonate blocks further have structural units which derive from bisphenol A.

7. The block cocondensate according to claim 1 , wherein the fraction of the siloxane blocks of the formula (2) in the block cocondensate is 0.5 to 20.0 wt %, based on the total weight of the block cocondensate.

8. Process for preparing the block cocondensate according to claim 1 , comprising the reaction of

(a) a (co)polycarbonate comprising structural units of the general formula (1)

(b) a hydroxyaryl-terminated polysiloxane of the formula (2b)

 where R 5 , R 6 , R 7 , V, W, Y, o, p, q and m have the same definition as in formula (2) according to claim 1 ;

(c) and a homopolycarbonate

in the melt.

9. The process according to claim 8 , wherein the homopolycarbonate has been prepared by the melt transesterification process.

10. The process according to claim 8 , wherein the homopolycarbonate has a number-average molecular weight of at least 2000 g/mol, and an OH end group content of 300 to 900 ppm.

11. The process according to claim 8 , wherein components (a) to (c) are present in the following amounts in the melt:

(a) 20 to 94.5 wt % of the (co)polycarbonate,

(b) 0.5 to 20 wt % of the hydroxyaryl-terminated polysiloxane, and

(c) 5 to 79.5 wt % of the homopolycarbonate,

based in each case on the total weight of the melt.

12. The process according to claim 8 , wherein the homopolycarbonate is based on bisphenol A and the copolycarbonate is based on bisphenol A and bisphenol TMC.

13. The block cocondensate according to claim 1 , obtained by reacting

(a) a (co)polycarbonate comprising structural units of the general formula (1)

 in which

R 1 and R 2 independently of one another are hydrogen, halogen, C 1 -C 8 alkyl, C 5 -C 6 cycloalkyl, phenyl or C 7 -C 12 aralkyl,

R 3 and R 4 for each X are individually selectable and independently of one another are hydrogen or C 1 -C 6 alkyl, and

n is an integer from 4 to 7,

X is carbon,

with the proviso that on at least one atom X R 3 and R 4 are C 1 -C 6 alkyl;

(b) a hydroxyaryl-terminated polysiloxane of the formula (2b)

R 5 is H,

R 6 and R 7 are each methyl,

V is O,

W is a single bond,

Y is isopropylidene,

m is an average number of repeat units from 2 to 5,

o is an average number of repeat units from 10 to 100,

q is 0, and

p is 0 or 1; and the product of m times o is a number between 15 and 200; and

(c) and a homopolycarbonate which contains no structural units of the formula (1) and has a number-average molecular weight M n of at least 2000 g/mol in the melt.

14. A method comprising utilizing the block cocondensates according to claim 1 for producing mouldings and extrudates.

15. A moulding or extrudate comprising a block cocondensate according to claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 5, 2017
From: MEYER, ALEXANDER; HORN, KLAUS
To: COVESTRO DEUTSCHLAND AG
Reel/Frame 043796/0238 →
Priority Claims (1)
EP 15162554 · Apr 7, 2015 · regional
Continuity (1)
Related Publication 20180079862A1 · Mar 22, 2018