IP Library Granted Patent US 6,987,153
Granted Patent B2
US 6,987,153 · App. 10/854,690 · Granted Jan 17, 2006

Latex binder for nonwoven fibers and article made therewith

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Quick Facts
Patent No.
US 6,987,153
App. No.
10/854,690
Granted
Jan 17, 2006
Kind
B2
Abstract

The invention relates to a latex that may be utilized as a binder for nonwoven applications to form a permeable sublayer of personal hygiene articles. The latex is prepared by a process including the steps of (1) polymerizing a monomer mixture comprising styrene, itaconic acid, surfactant and water soluble free radical initiator to form a seed; (2) sequentially adding equal increments of a monomer mixture of styrene, butadiene and acrylic acid to the seed under emulsion polymerization conditions to form a styrene-butadiene-acrylic acid copolymer; and then (3) neutralizing the styrene-butadiene-acrylic acid copolymer to a pH of about 4.5 to 7 to form the latex.

Claims (28)

1. A process for forming a polymer, the process comprising:

(i) adding a first monomer charge and a chain transfer agent to an aqueous system, where the first monomer charge includes styrene and butadiene;

(ii) initiating polymerization of the first monomer charge;

(iii) adding a second monomer charge and additional chain transfer agent to the aqueous system when 40 to 95% of the first monomer charge is converted, where the second monomer charge includes styrene, butadiene, and acrylic acid;

(iv) allowing the second monomer charge to polymerize; and

(v) neutralizing the aqueous system after 99% of the first and second monomer charge are converted.

2. The process of claim 1 , where the aqueous system to which the first monomer charge is added includes a polymeric seed.

3. The process of claim 2 , where the polymeric seed is formed by combining an initiator, styrene, and itaconic acid.

4. The process of claim 1 , where the first monomer charge includes functional monomer.

5. The process of claim 4 , where the second monomer charge includes functional monomer.

6. The process of claim 5 , where the functional monomer is selected from the group consisting of acrylates, acrylamides, acids, and mixtures thereof.

7. The process of claim 6 , where the functional monomer is selected from the group consisting of hydroxyethylacrylate, acrylamide, methacrylic acid, and N-methlolacrylamide, and mixtures thereof.

8. The process of claim 1 , where said step of adding the second monomer charge includes adding the second monomer charge in equal increments.

9. A process for forming a copolymer, the process comprising:

(i) forming a first segment of the copolymer by polymerizing a first charge of monomer including styrene and butadiene in the presence of a chain transfer agent; and

(ii) after converting from 40-95% of the first charge of monomer, forming an additional copolymer segment by polymerizing an additional charge of monomer including styrene, butadiene, and acrylic acid.

10. The process of claim 9 , where said step of forming the first segment occurs in the presence of a polymeric seed.

11. The process of claim 9 , where the first and additional monomer charge include functional monomer.

12. The process of claim 11 , where the functional monomer is selected from the group consisting of acrylates, acrylamides, acids, and mixtures thereof.

13. The process of claim 12 , where the functional monomer is selected from the group consisting of hydroxyethylacrylate, acrylamide, methacrylic acid, and N-methlolacrylamide, and mixtures thereof.

14. The process of claim 9 , where said step of forming an additional copolymer segment includes polymerizing additional monomer added by equal increment.

15. A process for forming a polymeric particle within an emulsion, the process comprising:

(i) forming a polymeric seed particle within an aqueous system;

(ii) adding a first monomer charge and a chain transfer agent to the aqueous system, where the first monomer charge includes styrene and butadiene;

(iii) initiating polymerization of the first monomer charge to thereby form polymeric particles that include styrene and butadiene repeat units;

(iv) adding a second monomer charge and additional chain transfer agent to the aqueous system when 40 to 95% of the first monomer charge is converted to the polymeric particles, where the second monomer charge includes styrene, butadiene, and acrylic acid;

(v) allowing the second monomer charge to polymerize and thereby increase the molecular weight of the first polymeric particles with repeat units that include styrene, butadiene, and acrylic acid; and

(vi) neutralizing the aqueous system after 99% of the first and second monomer charge is converted to polymeric particles.

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Apr 1, 2020
From: DEUTSCHE BANK AG NEW YORK BRANCH
To: OMNOVA SOLUTIONS INC.
Reel/Frame 052286/0911 →
RELEASE OF SECURITY INTEREST IN INTELLECTUAL PROPERTY COLLATERAL Recorded Apr 1, 2020
From: JPMORGAN CHASE BANK, N.A.
To: OMNOVA SOLUTIONS INC.
Reel/Frame 052286/0971 →
NOTICE OF SUCCESSION OF AGENCY OF REEL/FRAME 019597/0227 Recorded Aug 29, 2016
From: DEUTSCHE BANK TRUST COMPANY AMERICAS
To: DEUTSCHE BANK AG NEW YORK BRANCH, AS SUCCESSOR AGENT
Reel/Frame 039851/0696 →
SECURITY INTEREST Recorded Aug 26, 2016
From: OMNOVA SOLUTIONS INC.
To: JPMORGAN CHASE BANK, N.A., AS AGENT
Reel/Frame 039555/0403 →
GRANT OF SECURITY INTEREST IN CERTAIN PATENTS AND TRADEMARKS Recorded Jul 24, 2007
From: OMNOVA SOLUTIONS INC.
To: DEUTSCHE BANK TRUST COMPANY AMERICAS, AS COLLATERAL AGENT
Reel/Frame 019597/0227 →
SECURITY AGREEMENT Recorded May 30, 2007
From: OMNOVA SOLUTIONS INC.
To: JPMORGAN CHASE BANK, N.A.
Reel/Frame 019353/0566 →