IP Library Granted Patent US 11,787,901
Granted Patent B2
US 11,787,901 · App. 17/881,946 · Granted Oct 17, 2023

Polyester container and manufacturing method therefor

Inventors: Yoo Jin Lee (Gyeonggi-do, KR); Sung-Gi Kim (Gyeonggi-do, KR); Boo-Youn Lee (Gyeonggi-do, KR)
Assignee: SK Chemicals Co., Ltd.
C08G63/183B29C49/0005C08G63/672C08G63/80C08G63/863C08L67/02B29K2067/003B29L2031/7158C08G2390/00C08L2201/10C08L2203/10
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Quick Facts
Patent No.
US 11,787,901
App. No.
17/881,946
Granted
Oct 17, 2023
Kind
B2
Abstract

The present invention relates to a polyester container. The polyester container is formed from a polyester resin containing a particular content of diol moieties derived from isosorbide and diethylene glycol, and thus can show high transparency in spite of a great wall thickness thereof.

Claims (15)

1. A method of preparing a polyester container comprising the steps of:

(a) carrying out an esterification reaction or a transesterification reaction of (i) a dicarboxylic acid or a derivative thereof including terephthalic acid or a derivative thereof and (ii) a diol including 6.5 mol to 25 mol of isosorbide and 80 mol to 200 mol of ethylene glycol based on 100 mol of the total dicarboxylic acid or the derivative thereof;

b) subjecting the esterification or transesterification reaction product to a polycondensation reaction so that an intrinsic viscosity, which is measured at 35° C. after dissolving the reaction product in orthochlorophenol at a concentration of 1.2 g/dl at 150° C. for 15 minutes, reaches 0.60 dl/g to 0.75 dl/g, thereby providing a polyester resin;

(c) crystallizing the polyester resin;

(d) subjecting the crystallized polymer to a solid phase polymerization such that the intrinsic viscosity, which is measured at 35° C. after dissolving the polymer in orthochlorophenol at a concentration of 1.2 g/dl at 150° C. for 15 minutes, reaches a value of 0.25 dl/g to 0.40 dl/g higher than the intrinsic viscosity of the resin obtained in step (b); and

(e) molding a polyester container from the polyester resin,

wherein the intrinsic viscosity of the resin obtained in step (d) is 0.85 dl/g to 1.0 dl/g, and

wherein the polyester resin includes 6 mol % to 12 mol % of a diol moiety derived from isosorbide based on the total diol moieties derived from the diol.

2. The method of preparing the polyester container of claim 1 , wherein the (i) dicarboxylic acid or a derivative thereof is a dicarboxylic acid, and the initial mixing molar ratio of the (i) dicarboxylic acid: the (ii) diol is adjusted to 1:1.01 to 1.05, or

the (i) dicarboxylic acid or a derivative thereof is a dicarboxylic acid alkyl ester or a dicarboxylic acid anhydride, and the initial mixing molar ratio of the (i) dicarboxylic acid derivative: the (ii) diol is adjusted to 1:2.0 to 1:2.1.

3. The method of preparing the polyester container of claim 1 , wherein a part of the (ii) diol is further added during the (a) esterification reaction or the transesterification reaction.

4. The method of preparing the polyester container of claim 1 , wherein a polycondensation catalyst, a stabilizer, a coloring agent, a crystallizing agent, an antioxidant or a branching agent is added to a slurry before the start of the (a) esterification reaction or the transesterification reaction, or to the product after the completion of the reaction.

5. The method of preparing the polyester container of claim 1 , further comprising removing unreacted materials including isosorbide by allowing the product obtained by the esterification reaction or the transesterification reaction to stand under a reduced pressure condition of 400 to 1 mmHg for 0.2 to 3 hours, before the (b) polycondensation reaction.

6. The method of preparing polyester container of claim 2 , wherein a part of the (ii) diol is further added during the (a) esterification reaction or the transesterification reaction.

7. The method of preparing polyester container of claim 1 , wherein the polyester resin further includes 2 mol % to 5 mol % of a diol moiety derived from diethylene glycol, and remainder of a diol moiety derived from ethylene glycol based on the total diol moieties derived from (ii) the diol.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2022
From: LEE, YOO JIN; KIM, SUNG-GI; LEE, BOO-YOUN
To: SK CHEMICALS CO., LTD.
Reel/Frame 061474/0079 →
Priority Claims (1)
KR 10-2017-0079381 · Jun 22, 2017 · national
Continuity (2)
Division 16624148
Related Publication 20220380595A1 · Dec 1, 2022
Cited By (1)
US 12,392,057