IP Library Patent Application 17802240
Patent Application
App. No. 17/802,240

FLOOR FINISHING COMPOSITIONS WITH ENHANCED DURABILITY, METHODS OF MAKING AND USING THEREOF

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 None
App. No.
17/802,240
Abstract

A floor finishing composition comprises water, polymer of ethylenic unsaturated monomers having a glass transition temperature of at least 90#C as measured using differential scanning calorimetry according to the ASTM Method D3418-15, coalescing solvent, and polyvalent metal crosslinking agent. The ethylenic unsaturated monomers comprise methyl (meth)acrylate, α,β-unsaturated carboxylic acid, aromatic vinyl monomer, and no more than 25% by weight of α,β-unsaturated carboxylic ester of C2-10 alcohol based on total weight of the monomers. The ethylenic unsaturated monomers may comprise from about 14% to about 18% by weight of the α,β-unsaturated carboxylic acid based on total weight of the monomers. The amount of coalescing solvent in the floor finishing composition may be more than 6% by weight based on total weight of the floor finishing composition.

Claims (40)

1 . A floor finishing composition, comprising:

water;

polymer of ethylenic unsaturated monomers, wherein the polymer has a glass transition temperature of at least 105° C. and no more than 150° C. as measured using differential scanning calorimetry according to the ASTM Method D3418-15,

wherein the ethylenic unsaturated monomers comprise methyl (meth)acrylate, α,β-unsaturated carboxylic acid, aromatic vinyl monomer, and no more than 25% by weight of α,β-unsaturated carboxylic ester of C2-10 alcohol based on total weight of the monomers;

coalescing solvent; and

polyvalent metal crosslinking agent.

2 . The composition of claim 1 , wherein the ethylenic unsaturated monomers comprise from about 14% to about 18% by weight of the α,β-unsaturated carboxylic acid based on total weight of the monomers.

3 . The composition of claim 1 , wherein the ethylenic unsaturated monomers comprise less than 25% by weight of α,β-unsaturated carboxylic ester of C2-10 alcohol based on total weight of the monomers.

4 . The composition of claim 1 , wherein the α,β-unsaturated carboxylic acid comprises (meth)acrylic acid, maleic acid, fumaric acid, aconitic acid, crotonic acid, citraconic acid, acryloxypropionic acid, or any mixtures thereof.

5 . The composition of claim 1 , wherein the ethylenic unsaturated monomers comprise from about 15% to about 55% by weight of the methyl (meth)acrylate.

6 . The composition of claim 1 , wherein the ethylenic unsaturated monomers comprise from about 30% to about 50% by weight of the aromatic vinyl monomer based on total weight of the monomers.

7 . The composition of claim 1 , wherein the aromatic vinyl monomer comprises styrene, α-methylstyrene, β-methylstyrene, vinyl toluene, 1-vinyl naphthalene, 1-methylstyrene, 2-methylstyrene, 3-methylstyrene, 3,4-dimethylstyrene, 4-ethylstyrene, 2-chlorostyrene, 3-chlorostyrene, 1-bromostyrene, 2-bromostyrene, 4-chloro-3-methylstyrene, 4-t-butylstyrene, 2,4-dichlorostyrene, 2,6-dichlorostyrene, 1-methoxystyrene, 2-methoxystyrene, 4-methoxystyrene, allyl phenyl ether, allyl tolyl ether, or any mixtures thereof.

8 . The composition of claim 1 , wherein the α,β-unsaturated carboxylic ester of C2-10 alcohol comprises methyl (meth)acrylate, ethyl (meth)acrylate, n-propyl (meth)acrylate, iso-propyl (meth)acrylate, n-butyl (meth)acrylate, iso-butyl (meth)acrylate, t-butyl (meth)acrylate, n-amyl (meth)acrylate, iso-amyl (meth)acrylate, hexyl (meth)acrylate, cyclohexyl (meth)acrylate 2-ethyl hexyl (meth)acrylate, n-octyl methacrylate, iso-nonyl (meth)acrylate, decyl (meth)acrylate, or any mixtures thereof.

9 . The composition of claim 1 , wherein the ethylenic unsaturated monomers comprise:

from about 15% to about 55% by weight of the methyl (meth)acrylate;

from about 14% to about 16% by weight of the α,β-unsaturated carboxylic acid;

from about 30% to about 50% by weight of the aromatic vinyl monomer, and

no more than 25% by weight of the α,β-unsaturated carboxylic ester of C2-10 alcohol, all based on total weight of the monomers.

10 . The composition of claim 1 , wherein the coalescing solvent is present in an amount of at least 6% by weight based on total weight of the floor finishing composition.

11 . The composition of claim 1 , wherein the coalescing solvent fulfills at least one of the following:

(a) the coalescing solvent comprises alcohol, polyvalent alcohol, glycol ether, glycol ether esters, ester alcohols, or any mixtures thereof;

(b) the coalescing solvent comprises diethylene glycol monoethyl ether, diethylene glycol n-propyl ether, ethylene glycol 2-ethylhexyl ether, or any mixtures thereof.

12 . The composition of claim 1 , wherein the polyvalent metal crosslinking agent comprises zinc ammonium carbonate.

13 . The composition of claim 1 , wherein the polyvalent metal crosslinking agent is present in the range of from about 10% to about 100% theoretical mole stoichiometry based on the α,β-Unsaturated carboxylic acid monomer unit on the polymer.

14 . The composition of claim 1 , wherein the composition fulfills at least one of the following:

(a) the composition has a pH of from about 6 to about 10;

(b) the composition has a % solids content of from about 10% to about 30%;

(c) the composition further comprises plasticizer, alkaline soluble resin, wax, surfactant, dispersing agent, wetting agent, leveling agent, coating slip aid, defoamer, preservative, biocide, or any combinations thereof.

15 . A method of finishing a floor, comprising applying the floor finishing composition of claim 1 , to the floor surface.

16 . A method of using a polymer having a glass transition temperature of at least 105° C. and no more than 150° C. in floor finishing composition, wherein the glass transition temperature is measured using differential scanning calorimetry according to the ASTM Method D3418-15, and

wherein the polymer includes units derived from ethylenic unsaturated monomers comprising methyl (meth)acrylate, α,β-unsaturated carboxylic acid, aromatic vinyl monomer, and no more than 25% by weight of α,β-unsaturated carboxylic ester of C2-10 alcohol based on total weight of the monomers.

17 . The method of claim 16 , wherein the ethylenic unsaturated monomers fulfills at least one of the following:

(a) the monomers comprise from about 14% to about 18% by weight of the α,β-unsaturated carboxylic acid based on total weight of the monomers;

(b) the monomers comprise less than 25% by weight of α,β-unsaturated carboxylic ester of C2-10 alcohol based on total weight of the monomers;

(c) the monomers comprise from about 30% to about 50% by weight of the aromatic vinyl monomer based on total weight of the monomers;

(d) the monomers comprise from about 15% to about 55% by weight of the methyl (meth)acrylate.

18 . The method of claim 16 , wherein the α,β-unsaturated carboxylic acid comprises (meth)acrylic acid, maleic acid, fumaric acid, aconitic acid, crotonic acid, citraconic acid, acryloxypropionic acid, or any mixtures thereof.

19 . The method of claim 16 , wherein the aromatic vinyl monomer comprises styrene, α-methylstyrene, β-methylstyrene, vinyl toluene, 1-vinyl naphthalene, 1-methylstyrene, 2-methylstyrene, 3-methylstyrene, 3,4-dimethylstyrene, 4-ethylstyrene, 2-chlorostyrene, 3-chlorostyrene, 1-bromostyrene, 2-bromostyrene, 4-chloro-3-methylstyrene, 4-t-butylstyrene, 2,4-dichlorostyrene, 2,6-dichlorostyrene, 1-methoxystyrene, 2-methoxystyrene, 4-methoxystyrene, allyl phenyl ether, allyl tolyl ether, or any mixtures thereof.

20 . The method of claim 16 , wherein the α,β-unsaturated carboxylic ester of C2-10 alcohol comprises methyl (meth)acrylate, ethyl (meth)acrylate, n-propyl (meth)acrylate, iso-propyl (meth)acrylate, n-butyl (meth)acrylate, iso-butyl (meth)acrylate, t-butyl (meth)acrylate, n-amyl (meth)acrylate, iso-amyl (meth)acrylate, hexyl (meth)acrylate, cyclohexyl (meth)acrylate 2-ethyl hexyl (meth)acrylate, n-octyl methacrylate, iso-nonyl (meth)acrylate, decyl (meth)acrylate, or any mixtures thereof.

21 . (canceled)

Assignments (9)
RELEASE OF SECURITY INTEREST Recorded Nov 14, 2025
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
To: BIRKO CORPORATION; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 073564/0864 →
RELEASE OF 2023 NOTES PATENT SECURITY INTERESTS Recorded Oct 10, 2025
From: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
To: BIRKO CORPORATION; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
Reel/Frame 073074/0198 →
SECURITY AGREEMENT (NOTES) Recorded Oct 10, 2025
From: DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 073061/0885 →
SECURITY AGREEMENT (2024 NOTES) Recorded Jun 24, 2024
From: BIRKO CORPORATION; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE, LLC; SOLENIS TECHNOLOGIES, L.P.
To: THE BANK OF NEW YORK MELLON TRUST COMPANY, N.A., AS NOTES COLLATERAL AGENT
Reel/Frame 067824/0278 →
NOTES PATENT SECURITY AGREEMENT Recorded Jul 7, 2023
From: BIRKO CORPORATION; SOLENIS TECHNOLOGIES, L.P.; INNOVATIVE WATER CARE, LLC; DIVERSEY, INC.; DIVERSEY TASKI, INC.
To: BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
Reel/Frame 064348/0235 →
2023 NOTES PATENT SECURITY AGREEMENT Recorded Jul 7, 2023
From: BIRKO CORPORATION; SOLENIS TECHNOLOGIES, L.P.; INNOVATIVE WATER CARE, LLC; DIVERSEY, INC.; DIVERSEY TASKI, INC.; INNOVATIVE WATER CARE GLOBAL CORPORATION
To: BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
Reel/Frame 064225/0170 →
2021 NOTES PATENT SECURITY AGREEMENT Recorded Jul 7, 2023
From: BIRKO CORPORATION; SOLENIS TECHNOLOGIES, L.P.; INNOVATIVE WATER CARE, LLC; DIVERSEY, INC.; DIVERSEY TASKI, INC.
To: BANK OF NEW YORK MELLON TRUST COMPANY, N.A.
Reel/Frame 064225/0576 →
ABL PATENT SECURITY AGREEMENT Recorded Jul 6, 2023
From: BIRKO CORPORATION; SOLENIS TECHNOLOGIES, L.P.; INNOVATIVE WATER CARE, LLC; DIVERSEY, INC.; DIVERSEY TASKI, INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 064222/0751 →
TERM LOAN PATENT SECURITY AGREEMENT Recorded Jul 6, 2023
From: BIRKO CORPORATION; SOLENIS TECHNOLOGIES, L.P.; INNOVATIVE WATER CARE, LLC; DIVERSEY, INC.; DIVERSEY TASKI, INC.
To: GOLDMAN SACHS BANK USA
Reel/Frame 064223/0526 →