IP Library Granted Patent US 9,738,743
Granted Patent B2
US 9,738,743 · App. 15/174,422 · Granted Aug 22, 2017

Method for producing acrylic polymer, acrylic polymer, and plastisol composition

Inventor: Toru Kondo (Toyohashi, JP)
Assignee: Mitsubishi Chemical Corporation
C08F265/06C08F220/28C08K5/10C08K5/12C08L51/06
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 9,738,743
App. No.
15/174,422
Granted
Aug 22, 2017
Kind
B2
Abstract

Disclosed is a method for producing a plastisol acrylic polymer which can have a satisfactory adhesion property even when the heating time is short and the heating temperature is low, and which has excellent storage stability. The method comprises (1) a step of polymerizing an acrylic monomer mixture (a) to produce a polymer (A) and (2) a step of polymerizing an acrylic monomer mixture (b) in a dispersion containing the polymer (A), wherein a monomer having a hydroxy group is contained in the acrylic monomer mixture (a), a monomer having an acetoacetyl group or a block isocyanate group is contained in the acrylic monomer mixture (b), and the dissolution parameter (SA) for the polymer (A) and the dissolution parameter (SB) for a polymer (B) produced by the polymerization of the acrylic monomer mixture (b) are different from each other.

Claims (20)

1. An acrylic polymer obtained by

polymerizing an acrylic monomer mixture (a) to obtain a polymer (A); and

polymerizing an acrylic monomer mixture (b) in a dispersion comprising the polymer (A), wherein

the acrylic monomer mixture (a) comprises a monomer having a hydroxyl group,

the acrylic monomer mixture (b) comprises a monomer having an acetoacetyl group or a blocked isocyanate group, and

a solubility parameter (SA) of the polymer (A) is different from a solubility parameter (SB) of a polymer (B) obtained by polymerizing the acrylic monomer mixture (b),

wherein the acrylic monomer mixture (b) comprises the monomer having an acetoacetyl group or a blocked isocyanate group in an amount of 0.7 to 15 mol % based on 100 mol % of the acrylic monomer mixture (b),

wherein the acrylic monomer mixture (a) comprises the monomer having a hydroxyl group in an amount of 0.1 to 15 mol % based on 100 mol % of the acrylic monomer mixture (a), and

wherein the acrylic monomer mixture (a) further comprises methyl methacrylate, butyl methacrylate, or a combination thereof, in a total amount of 55 mol % or greater based on 100 mol % of the acrylic monomer mixture (a).

2. A plastisol composition comprising the acrylic polymer of claim 1 and a plasticizer.

3. The acrylic polymer of claim 1 , wherein the monomer having a hydroxyl group is at least one monomer selected from the group consisting of 2-hydroxyethyl (meth)acrylate, 2-hydroxypropyl (meth)acrylate, 3-hydroxypropyl (meth)acrylate, 2-hydroxybutyl (meth)acrylate, 3-hydroxybutyl (meth)acrylate, 4-hydroxybutyl (meth)acrylate, and dipentaerythritol hexa(meth)acrylate.

4. The acrylic polymer of claim 1 , wherein the monomer having a hydroxyl group is at least one monomer selected from the group consisting of 2-hydroxyethyl (meth)acrylate and 2-hydroxypropyl (meth)acrylate.

5. The acrylic polymer of claim 1 , wherein the acrylic monomer mixture (a) comprises the monomer having a hydroxyl group in an amount of 0.1 to 10 mol % based on 100 mol % of the acrylic monomer mixture (a).

6. The acrylic polymer of claim 1 , wherein the acrylic monomer mixture (a) further comprises methyl methacrylate and butyl methacrylate in a molar ratio within a range of from 20:80 to 75:25.

7. The acrylic polymer of claim 1 , wherein the acrylic monomer mixture (b) comprises a monomer having an acetoacetyl group.

8. The acrylic polymer of claim 1 , wherein the acrylic monomer mixture (b) comprises a monomer having a blocked isocyanate group.

9. The acrylic polymer of claim 7 , wherein the monomer having an acetoacetyl group is at least one monomer selected from the group consisting of 2-acetoacetoxyethyl (meth)acrylate, 2-acetoacetoxypropyl (meth)acrylate, 2-cyanoacetoacetoxyethyl methacrylate, N-(2-acetoxyaminoethyl) (meth)acrylamide, allyl acetoacetate, and vinyl acetoacetate.

10. The acrylic polymer of claim 8 , wherein the monomer having a blocked isocyanate group is at least one monomer selected from the group consisting of 2[(3,5-dimethylpyrazolyl)carbonylamino]ethyl methacrylate and 2-[O-(1′-methyl propylidene amino)carboxyamino]ethyl methacrylate.

11. The acrylic polymer of claim 1 , wherein the acrylic monomer mixture (b) comprises the monomer having an acetoacetyl group or a blocked isocyanate group in an amount of 0.7 to 9 mol % based on 100 mol % of the acrylic monomer mixture (b).

12. The acrylic polymer of claim 1 , wherein the monomer having a hydroxyl group is a (meth)acrylic acid ester having a hydroxyl group.

Assignments (1)
CHANGE OF NAME Recorded Jun 28, 2017
From: MITSUBISHI RAYON CO., LTD.
To: MITSUBISHI CHEMICAL CORPORATION
Reel/Frame 043028/0747 →
Priority Claims (1)
JP 2011-255168 · Nov 22, 2011 · national
Continuity (2)
Division 14360205
Related Publication 20160280830A1 · Sep 29, 2016