IP Library Granted Patent US 9,029,482
Granted Patent B2
US 9,029,482 · App. 13/707,775 · Granted May 12, 2015

Method for preparing polycondensation resin

Inventors: Tomomich Kanda (Yokohamashi, JP); Shimoda Tomoaki (Yokohamashi, JP); Bok Nam Jang (Uiwang-si, KR); Seung Hyun Jang (Uiwang-si, KR)
Assignee: Cheil Industries Inc.
C08F2/36C08G69/30C08G63/605C08G63/80C08G64/307C08G69/265
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Quick Facts
Patent No.
US 9,029,482
App. No.
13/707,775
Granted
May 12, 2015
Kind
B2
Abstract

Disclosed herein is a method for preparing a polycondensation resin. The method includes preparing a low degree condensate; and solid phase polymerizing the low degree condensate, wherein a granular molded article is introduced into the solid phase polymerization. The method enables efficient manufacture of high quality resins without problems such as agglomeration or scaling of a low degree condensate in pipes.

Claims (22)

1. A method for preparing a polycondensation resin, comprising:

preparing a low degree condensate; and

solid phase polymerizing the low degree condensate,

wherein a granular molded article is provided upon solid phase polymerization and wherein the granular molded article has a particle diameter of 3 mm to about 30 mm.

2. The method according to claim 1 , wherein the granular molded article is a granular compression-molded article of the low degree condensate.

3. The method according to claim 2 , wherein the granular molded article of the low degree condensate is prepared by compression molding of the low degree condensate at about 10 MPa to about 800 MPa.

4. The method according to claim 2 , wherein the solid phase polymerization is performed in a longitudinal tower type apparatus or a longitudinal tower type machine.

5. The method according to claim 1 , wherein the granular molded article is a granular molded article of a thermoplastic resin.

6. The method according to claim 5 , wherein the low degree condensate is prepared in the form of crystalline powder, and the crystalline powder of the low degree condensate and the granular molded article of the thermoplastic resin are mixed to carry out solid phase polymerization.

7. The method according to claim 5 , wherein the thermoplastic resin is end-capped with an end capping agent.

8. The method according to claim 6 , wherein the granular molded article of the thermoplastic resin is mixed in an amount of about 0.1 wt % to 10 wt % with respect to the crystalline powder of the low degree condensate.

9. The method according to claim 5 , wherein the granular molded article of the thermoplastic resin is the same kind as the low degree condensate.

10. The method according to claim 5 , wherein the granular molded article of the thermoplastic resin has an inherent viscosity of about 0.3 dl/g to about 5 dl/g as measured at a concentration of 0.5 g/dl.

11. The method according to claim 1 , wherein the polycondensation resin comprises a polyamide, polycarbonate or polyester resin.

12. The method according to claim 1 , wherein the solid phase polymerization has a maximum reaction temperature of about 170° C. to about 350° C.

13. The method according to claim 1 , wherein the low degree condensate is prepared by polycondensation of a dicarboxylic acid and a diamine, and the moisture content in a reaction system is about 15 wt % to about 35 wt % at the end of polycondensation.

14. The method according to claim 13 , wherein the preparing the low degree condensate is performed at a reaction temperature of about 230° C. to about 250° C.

15. The method according to claim 13 , wherein the preparing the low degree condensate is performed at a pressure ranging from about 1.5 MPa to about 3.5 MPa for a reaction time ranging from about 0.5 hours to about 4.0 hours.

16. The method according to claim 13 , wherein the low degree condensate is provided to solid phase polymerization after being discharged and cooled under an inert gas atmosphere and atmospheric pressure or less.

17. The method according to claim 16 , wherein the cooled low degree condensate has an inherent viscosity of about 0.07 dl/g to about 0.20 dl/g as measured at 25° C. and at a concentration of 0.5 g/dl in concentrated sulfuric acid, and 5 wt % reduction temperature of about 300° C. or more as measured by thermogravimetry under nitrogen atmosphere.

18. The method according to claim 16 , wherein the inert gas has an oxygen concentration of about 1% by volume or less, and, in the cooling, the low degree condensate is cooled to about 100° C. or less.

19. The method according to claim 13 , wherein the dicarboxylic acid comprises about 30 mol % to about 100 mol % of terephthalic acid and about 0 to about 70 mol % of dicarboxylic acid except for terephthalic acid, the diamine comprising about 50 mol % to about 100 mol % of a C 4 to C 25 aliphatic alkylene diamine and about 0 to about 50 mol % of a C 3 to C 25 cycloaliphatic diamine.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 30, 2017
From: SAMSUNG SDI CO., LTD.
To: LOTTE ADVANCED MATERIALS CO., LTD.
Reel/Frame 042114/0895 →
MERGER Recorded Jul 14, 2016
From: CHEIL INDUSTRIES INC.
To: SAMSUNG SDI CO., LTD.
Reel/Frame 039360/0858 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 7, 2012
From: KANDA, TOMOMICH; TOMOAKI, SHIMODA; JANG, BOK NAM; JANG, SEUNG HYUN
To: CHEIL INDUSTRIES INC.
Reel/Frame 029424/0792 →
Priority Claims (3)
JP 2011-273248 · Dec 14, 2011 · national
JP 2011-273252 · Dec 14, 2011 · national
JP 2011-273256 · Dec 14, 2011 · national
Continuity (1)
Related Publication 20130165621A1 · Jun 27, 2013