Use of an additive composition for the preparation of polycondensation polymers

Patent metadata

Field	Value
Publication number	US-10920069-B2
Application number	US-201716313234-A
Country	US
Kind code	B2
Filing date	Jun 12, 2017
Priority date	Jun 27, 2016
Publication date	Feb 16, 2021
Grant date	Feb 16, 2021

Abstract

The present invention relates to the use of an additive composition for the preparation of polycondensation polymers wherein the additive combination is present in the polycondensation reaction and wherein the additive combination comprises one or more compounds of the formula (A) wherein R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , and R 18 are independently selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert.-butyl, linear or branched pentyl, linear or branched hexyl, linear or branched heptyl, linear or branched octyl or linear and branched nonyl groups, and R 21 and R 22 are independently selected from the group consisting of hydrogen, methyl, O(C 1 -C 6 -Acyl) and O—R 3 , wherein R 3 is selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert.-butyl linear or branched pentyl, linear or branched hexyl, linear or branched heptyl, linear or branched octyl or linear and branched nonyl groups, and one or more sterically hindered organic phosphorous(lll) compounds selected from the group consisting of sterically hindered phenyl phosphonites and sterically hindered phosphites.

First claim

The invention claimed is:

1. A process for preparing a polycondensation polymer, the process comprising preparing the polycondensation polymer from a polycondensation reaction of monomers wherein an additive combination is present in the polycondensation reaction,
wherein the additive combination comprises one or more compounds of the formula (A)

wherein
R 11 , R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , and R 18 are independently selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert.-butyl, linear or branched pentyl, linear or branched hexyl, linear or branched heptyl, linear or branched octyl or linear and branched nonyl groups, and
R 21 and R 22 are independently selected from the group consisting of hydrogen, methyl, O(C 1 -C 6 -Acyl) and O—R 3 , wherein R 3 is selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert.-butyl linear or branched pentyl, linear or branched hexyl, linear or branched heptyl, linear or branched octyl or linear and branched nonyl groups, and
one or more sterically hindered organic phosphorous(III) compounds of formula (B)

wherein
each R 41 , R 42 , R 43 , R 44 , R 51 , R 52 , R 53 and R 54 , are independently selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert.-butyl linear or branched pentyl, linear or branched hexyl, linear or branched heptyl, linear or branched octyl or linear or branched nonyl, and cumyl groups, and
wherein the additive combination comprises a proportion of from 95% to 98% by weight of the compounds of the formula (A) and 2% to 5% by weight of the sterically hindered organic phosphorous(III) compounds based on the total amount of the additive combination, and wherein the additive combination is used in the presence of an acid.

2. The process as claimed in claim 1 , wherein the additive combination is present in the polycondensation reaction mixture before the polymerization reaction starts.

3. The process as claimed in claim 1 , wherein the additive combination is present in the polycondensation reaction mixture before the reaction temperature is higher than 100° C.

4. The process as claimed in claim 1 , wherein the polycondensation polymer is a polyamide or a polyester.

5. The process as claimed in claim 1 , wherein the sterically hindered organic phosphorous(III) compounds are sterically hindered phenyl phosphonites.

6. The process as claimed in claim 1 , wherein the sterically hindered organic phosphorous(III) compound is a compound of the formula (B1)

7. The process as claimed in claim 1 , wherein the compound of the formula (A) corresponds to formula (A1)

8. The process as claimed in claim 1 , wherein the additive combination is used in an amount of from 0.01 to 10 weight percent, relative to the weight of the polycondensation polymer prepared.

9. The process as claimed in claim 1 , wherein the additive combination is used in an amount of from 0.1 to 0.5 weight percent, relative to the weight of the polycondensation polymer prepared.

10. The process as claimed in claim 1 , wherein the acid is selected from the group consisting of acetic acid, adipic acid, paraterephthalic acid, isophthalic acid and benzoic acid or a mixture thereof.

11. The process as claimed in claim 1 , wherein the total amount of the acid is from 0.01 to 5 weight percent, relative to the weight of the polycondensation polymer prepared.

Assignees

• Clariant Plastics & Coatings Ltd

Inventors

• Steffanut Pascal
• Sidqi Mohamed
• Dongiovanni Ernesto
• Abrahmi Jerome

Classifications

• C08G69/16 Primary

  Preparatory processes · CPC title

• C08G63/00

  Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule (polyester-amides C08G69/44; polyester-imides C08G73/16) · CPC title

• C08K5/5393

  Phosphonous compounds, e.g. R—P(OR')2 · CPC title

• C08K5/526

  with hydroxyaryl compounds · CPC title

• C08K5/3435 Primary

  Piperidines · CPC title