Process for preparing polyamides

Patent metadata

Field	Value
Publication number	US-9315626-B2
Application number	US-201013514364-A
Country	US
Kind code	B2
Filing date	Dec 3, 2010
Priority date	Dec 8, 2009
Publication date	Apr 19, 2016
Grant date	Apr 19, 2016

Abstract

The present invention relates to a process for preparing a polyamide based on dicarboxylic acids and diamines, comprising the following stages:
A) providing an aqueous monomer mixture composed of dicarboxylic acids and diamines, where the molar ratio of dicarboxylic acids to diamines is adjusted such that, at the outlet of stage C), there is a molar deficiency of dicarboxylic acids or diamines of 1 to 10 mol %, based on the respective other component, B) transferring the aqueous mixture from stage A) into a continuous evaporator reactor in which diamines and dicarboxylic acids are converted at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar, C) transferring the mixture from stage B) into a separator which is operated at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar with removal of gaseous components, D) transferring the mixture from stage C) together with diamine or dicarboxylic acid in an amount suitable for compensation for the molar deficiency into a tubular reactor which is operated at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar, for a residence time in the range from 10 seconds to 30 minutes, E) transferring the mixture from stage D) into an extruder which is operated at a temperature in the range from 150 to 400° C. for a residence time in the range from 10 seconds to 30 minutes with removal of gaseous components through venting orifices.

First claim

The invention claimed is:

1. A process for preparing a polyamide based on dicarboxylic acids and diamines, which comprises:
A) providing an aqueous monomer mixture composed of dicarboxylic acids and diamines, where the molar ratio of dicarboxylic acids to diamines is adjusted such that, at the outlet of stage C), there is a molar deficiency of dicarboxylic acids or diamines of 1 to 10 mol %, based on the respective other component,
B) transferring the aqueous mixture from stage A) into a continuous evaporator reactor in which diamines and dicarboxylic acids are converted at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar,
C) transferring the mixture from stage B) into a separator which is operated at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar with removal of gaseous components,
D) transferring the mixture from stage C) together with diamine or dicarboxylic acid in an amount suitable for compensation for the molar deficiency into a tubular reactor which is operated at a temperature in the range from 100 to 370° C. and a pressure in the range from 1 to 50 bar, for a residence time in the range from 10 seconds to 30 minutes, and
E) transferring the mixture from stage D) into an extruder which is operated at a temperature in the range from 150 to 400° C. for a residence time in the range from 10 seconds to 30 minutes with removal of gaseous components through venting orifices.

2. The process according to claim 1 , wherein the extrusion is followed by a pelletizing step and solid phase postcondensation.

3. The process according to claim 1 , wherein water vapor and volatile dicarboxylic acids or diamines are removed in stage C) and are then separated by distillation, and an aqueous condensate enriched in dicarboxylic acid or diamine is recycled into one or both of stages A) and B).

4. The process according to claim 1 , wherein the evaporator reactor is a vertical tubular reactor through which the flow is from the top downward.

5. The process according to claim 1 , wherein the monomer mixture in stage A) consists of a dicarboxylic acid mixture of 60 to 88% by weight of terephthalic acid and 12 to 40% by weight of isophthalic acid, in which up to 20% by weight of the dicarboxylic acid mixture is optionally replaced by other dicarboxylic acids, and hexamethylenediamine, up to 20% by weight of which is optionally replaced by other C 2-30 -diamines.

6. The process according to claim 5 , wherein equimolar amounts of dicarboxylic acids and diamines are present in the monomer mixture, 0.5 to 15% by weight of the hexamethylenediamine used in stage A) is removed in gaseous form in the separator in stage C) and sufficient hexamethylenediamine is added in stage D) that the content of amino end groups in the polyamide obtained at the end of stage E) is 40 to 220 mmol/kg.

7. The process according to claim 5 , wherein sufficient diamine is metered in stage D) that the amino end group content is increased by at least 20 mmol/kg.

8. The process according to claim 1 , wherein a fiber, a filler, a dye, an assistant or a mixture thereof is supplied to the compounding directly in the extruder.

9. The process according to claim 1 , wherein the tubular reactor is equipped completely or partially with static mixers.

10. A vehicle which comprises the polyamide obtained according to the process of claim 1 .

11. An article which comprises the polyamide obtained according to the process of claim 1 , wherein the article is in the domestic sector, in the electrical sector, in the electronic sector, in the drinking water sector, in the heating sector, in the sanitary or bathroom sector or in the medical technology sector.

12. A metal substitute which comprises the polyamide obtained according to the process of claim 1 .

Assignees

• El-Toufaili Faissal-Ali
• Desbois Philippe
• Wollny Andreas
• Lawrenz Sven
• Schmidt Christian
• Basf Se

Inventors

• El-Toufaili Faissal-Ali
• Desbois Philippe
• Wollny Andreas
• Lawrenz Sven
• Schmidt Christian

Classifications

• C08G69/265 Primary

  from at least two different diamines or at least two different dicarboxylic acids · CPC title

• C08G69/28

  Preparatory processes · CPC title