IP Library Granted Patent US 10,889,733
Granted Patent B2
US 10,889,733 · App. 16/204,025 · Granted Jan 12, 2021

Coating composition for forming scratch-resistant layer having high strength for automobile exterior and method for coating automobile exterior using the same

Inventors: Jae Beom Ahn (Anyang-si, KR); Young Hoon Choi (Cheonan-si, KR); Dae Geun Oh (Cheonan-si, KR); Sung Do Kim (Cheonan-si, KR); Si Hyun Jeong (Asan-si, KR)
Assignee: NOROO BEE Chemical Co., Ltd.
C09D133/10C08G18/4063C08G18/6229C08G18/6233C09D5/00C09D7/63C09D133/066C09D175/06C08G63/912C08K5/29C08L33/08C08L67/04
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,889,733
App. No.
16/204,025
Granted
Jan 12, 2021
Kind
B2
Abstract

A coating composition may include 5 wt % to 20 wt % of a caprolactone-modified hyperbranched polyester polyol, the caprolactone-modified hyperbranched polyester polyol obtained from polyhydric alcohol including caprolactone triol, 30 wt % to 50 wt % of a first acrylic resin, the first acrylic resin having a hydroxyl group, 15 wt % to 25 wt % of a second acrylic resin, the second acrylic resin having a hydroxyl group and having a glass transition temperature higher than that of the first acrylic resin, and an extra solvent.

Claims (23)

1. A coating composition for forming a scratch-resistant layer having a high strength for automobile exterior, comprising:

5 wt % to 20 wt % of a caprolactone-modified hyperbranched polyester polyol, the caprolactone-modified hyperbranched polyester polyol obtained from polyhydric alcohol including caprolactone triol;

30 wt % to 50 wt % of a first acrylic resin, the first acrylic resin having a hydroxyl group;

15 wt % to 25 wt % of a second acrylic resin, the second acrylic resin having a hydroxyl group and having a glass transition temperature higher than that of the first acrylic resin; and

20 wt % to 40 wt % of a solvent,

wherein the first acrylic resin has a solid content of 60% to 70%, a weight average molecular weight of 5,000 to 12,000, and a glass transition temperature of 10° C. to 20° C.

2. The coating composition for automobile exterior of claim 1 , wherein the caprolactone-modified hyperbranched polyester polyol has an acid value of 10 mg/KOH or less, and a weight average molecular weight of 1,000 to 2,000.

3. The coating composition for automobile exterior of claim 2 , wherein the caprolactone-modified hyperbranched polyester polyol is obtained by reacting a polybasic acid or a derivative thereof, a diol compound and the caprolactone triol.

4. The coating composition for automobile exterior of claim 3 , wherein the polybasic acid or a derivative thereof includes at least one selected from the group consisting of terephthalic acid, phthalic acid, phthalic anhydride, dimethylterephthalic acid, naphthalene dicarboxylate, tetrachlorophthalic acid, terephthalic acid bisglycol ester, isophthalic acid, t-butyl isophthalic acid, fumaric acid, adipic acid, azelaic acid, sebacic acid, dodecanoic acid, glutaric acid, succinic acid, oxalic acid, itaconic acid, dimeric fatty acid, maleic anhydride, succinic acid anhydride, chlorendic acid, diglycolic acid, pimelic acid, suberic acid, 1,4-cyclohexanedicarboxylic acid, 1,3-cyclohexanedicarboxylic acid, hexahydrophthalic anhydride and dimethyl cyclohexanedicarboxylate.

5. The coating composition for automobile exterior of claim 3 , wherein the diol compound includes at least one selected from the group consisting of 1,6-hexanediol, 2-butyl-2-ethyl-1,3-propanediol, 1,4-cyclohexanedimethanol, diethylene glycol, 1,3-propanediol, ethylene glycol, propylene glycol, 2,4-dimethyl-2-ethylhexane-1,3-diol, 2-ethyl-2-isobutyl-1,3-propanediol, 1,3-butanediol, 1,4-butanediol, 1,5-pentanediol, 3-methyl-1,5-pentanediol, methylpropanediol, 2-methyl-1,3-propanediol, dipropylene glycol and 1,9-nonanediol.

6. The coating composition for automobile exterior of claim 1 , wherein the first acrylic resin is obtained by a radical polymerization of a monomer mixture including aliphatic methacrylate of 20 wt % to 50 wt %, methacrylate having a hydroxyl group of 20 wt % to 50 wt %, (meth)acrylic acid of 0.1 wt % to 3 wt %, aliphatic acrylate of 5 wt % to 20 wt %, caprolactone-modified (meth)acrylate of 10 wt % to 20 wt % and aromatic acrylate of 10 wt % to 20 wt %.

7. The coating composition for automobile exterior of claim 1 , wherein the second acrylic resin has a solid content of 55% to 65%, a weight average molecular weight of 8,000 to 20,000, and a glass transition temperature of 40° C. to 50° C.

8. The coating composition for automobile exterior of claim 7 , wherein the second acrylic resin is obtained by a radical polymerization of a monomer mixture including aliphatic methacrylate of 20 wt % to 50 wt %, methacrylate having a hydroxyl group of 20 wt % to 40 wt %, (meth)acrylic acid of 0.1 wt % to 3 wt %, aliphatic acrylate of 5 wt % to 20 wt % and aromatic acrylate of 10 wt % to 25 wt %.

9. The coating composition for automobile exterior of claim 1 , wherein the solvent includes an alcohol-based solvent.

10. The coating composition for automobile exterior of claim 1 , further comprising:

at least one selected from the group consisting of a wetting agent, a light stabilizer and a reaction catalyst.

11. A method for coating automobile exterior, comprising:

pretreating a surface of an object to be coated;

forming a base coating layer on the surface of the object to be coated;

forming a color layer on the base coating layer;

coating a mixture of the coating composition of claim 1 and a curing agent on the color layer; and

heat-treating the coated mixture to form a cured coating layer.

12. The method of claim 11 , the curing agent includes a hexamethylene diisocyanate trimer.

Assignments (2)
MERGER Recorded Oct 12, 2023
From: NORO BEE CHEMICAL CO., LTD.
To: NOROO AUTOMOTIVE COATINGS CO., LTD.
Reel/Frame 065196/0589 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2018
From: AHN, JAE BEOM; CHOI, YOUNG HOON; OH, DAE GEUN; KIM, SUNG DO; JEONG, SI HYUN
To: NOROO BEE CHEMICAL CO., LTD.
Reel/Frame 047668/0101 →
Priority Claims (1)
KR 10-2017-0170743 · Dec 12, 2017 · national
Continuity (1)
Related Publication 20190177569A1 · Jun 13, 2019