IP Library Patent Application 11996631
Patent Application
App. No. 11/996,631

AQUEOUS DISPERSION OF STRUCTURED POLYMER, MANUFACTURING PROCESS AND USE IN COATING FORMULATIONS

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Patent No.
US None
App. No.
11/996,631
Abstract

The invention concerns the field of aqueous dispersions. It concerns in particular an aqueous dispersion based on structured polymer comprising at least two phases, one called soft with low Tg and the other called hard with high Tg. The invention also concerns the use of such dispersions, as binder in formulation for paints free of solvents or coalescent agents.

Claims (32)

1 . An aqueous dispersion of polymers in the form of structured particles with a mean diameter of between 70 and 300 nm comprising at least one first polymer exhibiting a glass transition temperature (Tg1) of between −50° C. and 0° C., representing from 30 to 70% by weight of the total weight of the particles, and at least one second polymer having a glass transition temperature (Tg2) of between 10 and 80° C., representing from 70 to 30% by weight of the total weight of the particles, wherein the Tg2−Tg1 is greater than or equal to 40° C.

2 . The aqueous dispersion of claim 1 , wherein the first polymer and the second polymer are prepared from a monomer mixture comprising at least one ethylenically unsaturated monomer chosen from (meth)acrylic acid esters and vinyl monomers.

3 . The aqueous dispersion of claim 1 , wherein the first polymer and the second polymer are prepared from a mixture of monomers comprising:

a. from 5 to 90% by weight of at least one monomer (a) chosen from styrene or methyl methacrylate,

b. from 10 to 95% by weight of at least one monomer (b) chosen from C 4 -C 10 esters of acrylic acid, and

c. from 0 to 5% by weight of at least one functional monomer.

4 . The aqueous dispersion of claim 3 , wherein the first polymer is prepared from a mixture comprising:

i. from 5 to 45% of at least one monomer (a),

ii. from 55 to 95% of at least one monomer (b), and

iii. from 0 to 5% of at least one monomer (c).

5 . The aqueous dispersion of claim 3 , wherein the second polymer is prepared from a mixture comprising:

i. from 55 to 90% of at least one monomer (a),

ii. from 10 to 45% of at least one monomer (b), and

iii. from 0 to 5% of at least one monomer (c).

6 . The aqueous dispersion of claim 1 , wherein Tg2−Tg1 is between 45 and 100° C.

7 . A process for the preparation of the aqueous dispersion of claim 1 , comprising:

a. combining a first mix of monomers in a first polymerization stage to prepare a first polymer, and;

b. combining a second mixture of monomers in a second polymerization stage to prepare a second polymer;

wherein one of the first polymer or the second polymer exhibit a Tg from −50° C. and 0° C. and the other of the first polymer or the second polymer has a Tg from 10° C. and 80° C., and

wherein one of the first polymer or the second polymer represents from 30 to 70% by weight of the total weight of the polymer and the other of the first polymer or the second polymer represents from 70 to 30% by weight of the total weight of the polymer.

8 . The process of claim 7 , wherein the polymer particles have a mean diameter of between 70 and 300 nm.

9 . The process of claim 7 , wherein the introduction of the monomers for the second polymerization stage begins when the conversion of the monomers of the first polymerization stage is greater than 95%.

10 . The process of claim 7 , wherein the polymerization of the second polymerization stage is initiated by a redox system comprising an oxidizing agent and a reducing agent at a temperature of between 40 and 95° C.

11 . The process of claim 10 , wherein the oxidizing agent is chosen from the group consisting of peroxides and hydroperoxides.

12 . The process of claim 10 , wherein the oxidizing agent is introduced during the first polymerization stage.

13 . (canceled)

14 . A paint formulation comprising the aqueous dispersion of claim 1 , wherein the paint formulation is devoid of a solvent and of a coalescening agent.

15 . The aqueous dispersion of claim 3 , wherein the C 4 -C 10 esters of acrylic acid are comprise n-butyl acrylate or 2-ethylhexyl acrylate.

16 . The aqueous dispersion of claim 3 , wherein the at least functional monomer is selected from the group consisting of acrylic acid, methacrylic acid, itaconic acid, fumaric acid, hydroxyethyl acrylate, hydroxyethyl meth-acrylate, acrylamide, methacrylamide, the sodium salt of 1 allyloxy-2 hydroxypropyl-sulphonate, the sodium salt of 1 methallyloxy-2 hydroxypropylsulphonate, 1 methacrylamido-2 imidazolidinoneethane and combinations thereof.

17 . The process of claim 11 , wherein the oxidizing agent comprises T-butyl perbenzoate or T-butyl hydroperoxide.

18 . The aqueous dispersion of claim 1 , wherein the aqueous dispersion is devoid of a solvent and a coalescening agent.

19 . The aqueous dispersion of claim 1 , wherein the first polymer and the second polymer are mutually incompatible.

Assignments (9)
RELEASE OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (030146/0970) Recorded Jul 9, 2019
From: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT AND COLLATERAL AGENT
To: HEXION INC. (FORMERLY KNOWN AS MOMENTIVE SPECIALTY CHEMICALS INC.)
Reel/Frame 049706/0264 →
RELEASE OF SECURITY INTEREST Recorded Feb 23, 2017
From: WILMINGTON TRUST, NATIONAL ASSOCIATION (SUCCESSOR BY MERGER TO WILMINGTON TRUST FSB), AS COLLATERAL AGENT
To: HEXION INC. (FORMERLY KNOWN AS HEXION SPECIALTY CHEMICALS INC.); BORDEN CHEMICAL FOUNDRY, LLC; HEXION INVESTMENTS INC. (FORMERLY KNOWN AS BORDEN CHEMICAL INVESTMENTS, INC.); HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; HEXION INTERNATIONAL INC. (FORMERLY KNOWN AS BORDEN CHEMICAL INTERNATIONAL INC.); OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
Reel/Frame 041793/0001 →
PATENT SECURITY AGREEMENT Recorded Apr 3, 2013
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 030146/0970 →
PATENT SECURITY AGREEMENT Recorded Apr 3, 2013
From: MOMENTIVE SPECIALTY CHEMICALS INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 030146/0946 →
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENT RIGHTS Recorded Mar 28, 2013
From: JPMORGAN CHASE BANK, N.A.
To: MOMENTIVE SPECIALTY CHEMICALS INC. (F/K/A HEXION SPECIALTY CHEMICALS, INC.)
Reel/Frame 030111/0021 →
CHANGE OF NAME Recorded Mar 5, 2012
From: HEXION SPECIALTY CHEMICALS, INC.
To: MOMENTIVE SPECIALTY CHEMICALS INC.
Reel/Frame 027808/0408 →
SECURITY AGREEMENT Recorded Feb 5, 2010
From: HEXION LLC; HEXION SPECIALTY CHEMICALS, INC.; BORDEN CHEMICAL FOUNDRY, LLC; BORDEN CHEMICAL INVESTMENTS, INC.; HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; BORDEN CHEMICAL INTERNATIONAL, INC.; OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 023905/0451 →
SECURITY INTEREST Recorded Jan 29, 2010
From: HEXION SPECIALTY CHEMICALS, INC.; BORDEN CHEMICAL FOUNDRY, LLC; BORDEN CHEMICAL INVESTMENTS, INC.; HEXION U.S. FINANCE CORP.; HSC CAPITAL CORPORATION; LAWTER INTERNATIONAL INC.; BORDEN CHEMICAL INTERNATIONAL, INC.; OILFIELD TECHNOLOGY GROUP, INC.; HEXION CI HOLDING COMPANY (CHINA) LLC
To: WILMINGTON TRUST FSB, AS COLLATERAL AGENT
Reel/Frame 023963/0038 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 1, 2008
From: AGNELY, MATHIAS; BZDUCHA, WOJCIECH; CADIX, ARNAUD; COLOMBET, JEAN-FRANCOIS
To: HEXION SPECIALTY CHEMICALS, INC.
Reel/Frame 020885/0545 →