IP Library Granted Patent US 8,133,958
Granted Patent B2
US 8,133,958 · App. 11/960,861 · Granted Mar 13, 2012

Methacrylate resin with excellent discoloration-resistance and transparency and method for preparing the same

Assignee: Cheil Industries Inc.
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Quick Facts
Patent No.
US 8,133,958
App. No.
11/960,861
Granted
Mar 13, 2012
Kind
B2
Abstract

One aspect of the invention relates to a methacrylate resin prepared by suspension polymerization using a polyalkylacrylate-acrylic acid as a suspension stabilizer. The suspension stabilizer is used in an amount of about 0.05 to about 0.25 parts by weight per 100 parts by weight of a monomer mixture. Another aspect of the invention relates to a method for preparing a methacrylate resin, which comprises: preparing a mixture by mixing an initiator and a chain-transfer agent with a monomer mixture comprising at least about 50% by weight of alkyl methacrylate; and adding the mixture to an aqueous solution of polyalkylacrylate-acrylic acid to conduct suspension polymerization.

Claims (16)

1. A methacrylate resin prepared by suspension polymerization wherein a polyalkylacrylate-acrylic acid selected from the group consisting of is used as a suspension stabilizer, wherein said suspension stabilizer is used in an amount of about 0.05 to about 0.25 parts by weight per 100 parts by weight of a monomer mixture used to prepare of the said methacrylate resin.

2. The methacrylate resin of claim 1 , wherein said monomer mixture comprises about 50 to about 100% by weight of an alkyl methacrylate, and about 0 to about 50% by weight of a monomer copolymerizable with the alkyl methacrylate.

3. The methacrylate resin of claim 2 , wherein the monomer copolymerizable with the alkyl methacrylate comprises a monomer selected from the group consisting of methacrylic acid ester monomers; acrylic acid ester monomers; unsaturated carboxylic acid monomers; acid anhydride monomers; hydroxyl group containing ester monomers; amide monomers; nitrile monomers; allyl glycidyl ethers; glycidyl methacrylates; styrenic monomers; and combinations thereof.

4. The methacrylate resin of claim 3 , wherein said methacrylic acid ester monomer comprises a monomer selected from the group consisting of ethyl methacrylate, propyl methacrylate, butyl methacrylate, and benzyl methacrylate; said acrylic acid ester monomer comprises a monomer selected from the group consisting of methyl acrylate, ethyl acrylate, propyl acrylate, butyl acrylate, and 2-ethyl hexyl acrylate; said unsaturated carboxylic acid monomer comprises a monomer selected from the group consisting of acrylic acid and methacrylic acid; said acid anhydride monomer comprises maleic anhydride; said hydroxyl group containing ester monomer comprises a monomer selected from the group consisting of 2-hydroxyethyl acrylate, 2-hydroxypropyl acrylate, and monoglycerol acrylate; said amide monomer comprises a monomer selected from the group consisting of acryl amide and methacryl amide; said nitrile monomer comprises a monomer selected from the group consisting of acrylonitrile and methacrylonitrile; and said styrenic monomer comprises a monomer selected from the group consisting of styrene and α-methyl styrene.

5. The methacrylate resin of claim 2 , wherein said alkyl methacrylate is methyl methacrylate, ethyl methacrylate, propyl methacrylate, or butyl methacrylate.

6. The methacrylate resin of claim 1 , wherein said methacrylate resin has a weight average molecular weight of from about 15,000 to about 200,000.

7. The methacrylate resin of claim 1 , wherein said methacrylate resin has a Yellow Index according to ASTM D-1925 of about 0.9 or less, a total light transmittance at a sample thickness of 3.0 mm of about 92% or more and a haze of about 0.6 or less.

8. A method for preparing a methacrylate resin of claim 1 , comprising:

preparing a mixture by mixing an initiator and a chain-transfer agent with a monomer mixture comprising at least about 50% by weight of alkyl methacrylate; and

adding the mixture to an aqueous solution of polyalkylacrylate-acrylic acid selected from the group consisting of polyethylacrylate-acrylic acid and polyethyl-hexylacrylate-acrylic acid under conditions to conduct suspension polymerization.

9. The method of claim 8 , wherein said aqueous solution of polyalkylacrylate-acrylic acid further comprises a suspension stabilization aid.

10. The method of claim 8 , wherein said polymerization is conducted at about 70 to about 120° C. for about 2 to about 8 hours.

11. The method of claim 8 , wherein said polymerization is conducted in the presence of additives selected from the group consisting of lubricants, ultraviolet absorbents, dyes, antioxidants, and combinations thereof.

12. The methacrylate resin of claim 1 , wherein said methacrylate resin has a Yellow Index according to ASTM D-1925 of about 0.1 to about 0.85, a total light transmittance at a sample thickness of 3.0 mm of about 93 to about 99% and a haze of about 0.1 to about 0.55.

13. The method of claim 8 , wherein said suspension polymerization is initiated after the mixture of initiator, chain-transfer agent and monomer mixture is added to the aqueous solution of polyalkylacrylate-acrylic acid.

14. The method of claim 8 , wherein said suspension stabilizer is used in an amount of about 0.05 to about 0.25 parts by weight per 100 parts by weight of said monomer mixture.

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 20, 2007
From: JEONG, JAE HOON; HA, DOO HAN; JANG, JUNG HO
To: CHEIL INDUSTRIES INC.
Reel/Frame 020280/0067 →
Priority Claims (2)
KR 10-2006-133967 · Dec 26, 2006 · national
KR 10-2007-106076 · Oct 22, 2007 · national
Continuity (1)
Related Publication 20080154008A1 · Jun 26, 2008