Preparation of siloxane-containing block copolycarbonates by means of reactive extrusion

US9828462B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9828462-B2
Application numberUS-201415027750-A
CountryUS
Kind codeB2
Filing dateOct 6, 2014
Priority dateOct 8, 2013
Publication dateNov 28, 2017
Grant dateNov 28, 2017

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present invention relates to a process for preparing polysiloxane-polycarbonate block cocondensates proceeding from specific polycarbonates and hydroxyaryl-terminated polysiloxanes. More particularly, the present invention relates to the preparation of the said block cocondensates by means of a reactive extrusion.

First claim

Opening claim text (preview).

The invention claimed is: 1. A process for preparing polysiloxane-polycarbonate block cocondensates, comprising reacting at least one hydroxyaryl-terminated polydialkylsiloxane with at least one polycarbonate in the melt, wherein the process is conducted in at least two stages in a reactor combination consisting of at least one preliminary reactor and a high-viscosity reactor and a discharge unit, wherein the material temperature in the high-viscosity reactor is within the range of from 330° C. to 370° C. and the pressure is within the range of from 0.03 to 5 mbar. 2. The process according to claim 1 , wherein the preliminary reactor consists of a single- or twin-screw extruder. 3. The process according to claim 1 , wherein the high-viscosity reactor has two or more shafts which rotate in parallel, on which there are axially offset, circular discs with strippers distributed on the circumference thereof. 4. The process according to claim 1 , wherein the discharge unit used is a single-screw screw, twin-screw screw or a gear pump. 5. The process according to claim 1 , wherein the material temperature in the preliminary reactor is within the range of from 300° C. to 380° C. and the pressure in the preliminary reactor is at least temporarily within the range of from 200 to 0.1 mbar. 6. The process according to claim 1 , wherein the residence time in the high-viscosity reactor is less than 50 minutes. 7. The process according to claim 1 , wherein the polycarbonate has a weight-average molecular weight of 16 000 to 28 000 g/mol and an OH end group content of 300 to 900 ppm. 8. The process according to claim 1 , wherein the hydroxyaryl-terminated polydialkylsiloxane has the structure (1) in which R 1 is H, Cl, Br or C 1 to C 4 -alkyl, R 2 and R 3 are the same or different and each independently from one another selected from aryl, C 1 to C 10 -alkyl and C 1 to C 10 -alkylaryl, X is a single bond, —CO—, —O—, C 1 to C 6 -alkylene, C 2 to C 5 -alkylidene, C 5 to C 12 -cycloalkylidene or C 6 to C 12 -arylene which may optionally be fused to further aromatic rings containing heteroatoms, n is a number from 1 to 500, m is a number from 1 to 10, and p is 0 or 1. 9. The process according to claim 8 , wherein n is a number from 10 to 100 and m is a number from 2 to 5. 10. The process according to claim 1 , wherein the hydroxyaryl-terminated polydialkylsiloxane has a weight-average molecular weight of 3000-20 000 g/mol. 11. The process according to claim 1 , wherein a phosphonium catalyst of the formula of the formula (5) is used during the reaction: where R a , R b , R c and R d may be identical or different C 1 -C 10 -alkyls, C 6 -C 14 -aryls, C 7 -C 15 -arylalkyls or C 5 -C 6 -cycloalkyls, and Y- may be an anion selected from the group consisting of hydroxide, sulphate, hydrogensulphate, hydrogencarbonate, carbonate, halide or an alkoxide or aroxide of the formula -OR e where R e is C 6 -C 14 -aryl, C 7 -C 15 -arylalkyl or C 5 -C 6 -cycloalkyl. 12. The process according to claim 1 , wherein the catalyst used is tetraphenylphosphonium phenoxide. 13. The process according to claim 1 , wherein the hydroxyaryl-terminated polydialkylsiloxane is used in an amount of 2 to 20%, based on the polycarbonate used. 14. The process according to claim 1 , wherein the siloxane and the polycarbonate are reacted in the presence of at least one organic or inorganic salt of an acid having a pK A value within the range of from 3 to 7 (25 ° C.).

Assignees

Inventors

Classifications

  • Gear pumps · CPC title

  • Phosphorus bound to carbon only · CPC title

  • General preparatory processes · CPC title

  • containing polycarbonate sequences · CPC title

  • C08G64/186Primary

    containing polysiloxane sequences · CPC title

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Frequently asked questions

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What does patent US9828462B2 cover?
The present invention relates to a process for preparing polysiloxane-polycarbonate block cocondensates proceeding from specific polycarbonates and hydroxyaryl-terminated polysiloxanes. More particularly, the present invention relates to the preparation of the said block cocondensates by means of a reactive extrusion.
Who is the assignee on this patent?
Covestro Deutschland Ag
What technology area does this patent fall under?
Primary CPC classification C08G64/186. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Nov 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).