Synthesis of re-pulpable temporary wet strength polymer for tissue application

US11345807B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11345807-B2
Application numberUS-201916668297-A
CountryUS
Kind codeB2
Filing dateOct 30, 2019
Priority dateNov 2, 2018
Publication dateMay 31, 2022
Grant dateMay 31, 2022

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

A grafted polyvinyl alcohol polymer has a balance between hydrophilicity and hydrophobicity. The grafted polyvinyl alcohol polymer has a chemical functionality that allows for adsorption onto the pulp fibers, polymer film formation upon drying, repelling water upon wetting, polymer film swelling and breaking for prolonged wetting by water. When incorporated into paper products, the polymer can provide a paper having improved wet strength, temporary water repellency, and/or is dispersible in aqueous solutions.

First claim

Opening claim text (preview).

What is claimed is: 1. A grafted polyvinyl alcohol polymer comprising a polyvinyl alcohol main chain and a plurality of side chains grafted to the polyvinyl alcohol main chain, wherein one or more of said side chains from the plurality of side chains comprise: i) one or more units selected from: an aliphatic monocarboxylic acid, an aliphatic dicarboxylic acid, and a reactive quaternary ammonium salt; and, ii) units of a branched alkyl acrylate. 2. The grafted polyvinyl alcohol polymer according to claim 1 , wherein at least 75%, by numerical number of said side chains from the plurality of side chains comprise: i) said one or more units selected from: the aliphatic monocarboxylic acid, the aliphatic dicarboxylic acid, and the reactive quaternary ammonium salt; and, ii) said units of the branched alkyl acrylate. 3. The grafted polyvinyl alcohol polymer according to claim 1 , wherein not more than 25%, by numerical number of side chains, from the plurality of side chains comprise units of the aliphatic amide, or units of the branched alkyl acrylate, or any combinations thereof, and have no units of the aliphatic monocarboxylic acid, of the aliphatic dicarboxylic acid, and of the reactive quaternary ammonium salt. 4. The grafted polyvinyl alcohol polymer according to claim 1 , wherein one or more of said side chains from the plurality of side chains further comprise units of an aliphatic amide. 5. The grafted polyvinyl alcohol polymer according to claim 1 , wherein side chains from the plurality of side chains comprise: i) said units of the reactive quaternary ammonium salt. 6. The grafted polyvinyl alcohol polymer according to claim 5 , wherein at least 75%, by numerical number of side chains, from the plurality of side chains comprise: i) said units of the reactive quaternary ammonium salt. 7. The grafted polyvinyl alcohol polymer according to claim 5 , wherein one or more of said side chains from the plurality of side chains further comprise units of an aliphatic amide. 8. The grafted polyvinyl alcohol polymer according to claim 1 , wherein side chains from the plurality of side chains comprise: i) said one or more units selected from: the aliphatic monocarboxylic acid and the aliphatic dicarboxylic acid. 9. The grafted polyvinyl alcohol polymer according to claim 1 , wherein the polyvinyl alcohol main chain, in unreacted form, has a monomodal molecular weight distribution of from about 5K to 20000K Daltons. 10. The grafted polyvinyl alcohol polymer according to claim 1 , wherein the polyvinyl alcohol main chain, in unreacted form, has a degree of hydrolysis of from about 74 mol % to about 99 mol %. 11. The grafted polyvinyl alcohol polymer according to claim 1 , wherein the polyvinyl alcohol main chain, in unreacted form, has a degree of hydrolysis of from about 74 mol % to about 90 mol %. 12. The grafted polyvinyl alcohol polymer according to claim 1 , wherein one or more of said side chains from the plurality of side chains are grafted to the polyvinyl alcohol main chain through acetate moieties of the polyvinyl alcohol main chain. 13. The grafted polyvinyl alcohol polymer according to claim 1 , wherein one or more of said side chains from the plurality of side chains are grafted to the polyvinyl alcohol main chain through hydroxyl moieties of the polyvinyl alcohol main chain. 14. The grafted polyvinyl alcohol polymer according to claim 4 , wherein the reactive quaternary ammonium salt is at least one of diallyl dimethyl ammonium chloride, 3-acrylamido propyl trimethyl ammonium chloride or combination of thereof; wherein the aliphatic amide comprises at least one of acrylamide, methacrylamide, dimethyl acrylamide, diethyl acrylamide, dipropyl acrylamide and N-t-butylacrylamide; and wherein the branched alkyl acrylate comprises at least one of 2-ethylheptyl acrylate, 2-ethylhexylacrylate, 2-ethylpentyl acrylate and 2-ethylbutyl acrylate. 15. The grafted polyvinyl alcohol polymer according to claim 1 , which is or comprises structure (I): [CH 2 —CH(OH)] a —[CH 2 —CH(R)] b   (I) wherein a total weight percent of (a) units is from 74% to 84% based on the total weight of the grafted polyvinyl alcohol polymer, wherein a total weight percent of (b) units is from 16% to 26% based on the total weight of the grafted polyvinyl alcohol polymer, wherein each R is acetate or a side chain from the plurality of side chains. 16. A grafted polyvinyl alcohol polymer comprising a polyvinyl alcohol main chain and a plurality of side chains grafted to the polyvinyl alcohol main chain, wherein one or more of said side chains from the plurality of side chains comprise: a reactive quaternary ammonium salt, units of an aliphatic amide, and a branched alkyl acrylate, and said grafted polyvinyl alcohol polymer having a polyvinyl alcohol main chain weight percent of about 40% to about 50%, by total solid weight; a reactive quaternary ammonium salt side chain weight percent of about 6% to about 10% by total solid weight; an aliphatic amide weight percent from about 6% to about 9% by total solid weight; and a branched alkyl acrylate weight percent from about 24% to about 50% by total solid weight. 17. A grafted polyvinyl alcohol polymer which is or comprises structure wherein the total weight percent of a is 30% to 34% based on the total weight of the grafted polyvinyl alcohol polymer, the total weight percent of b is 6% to 10% based on the total weight of the grafted polyvinyl alcohol polymer, the total weight percent of c is 0.5% to 1.0% based on the total weight of the grafted polyvinyl alcohol polymer, and the total weight percent of d is 58% to 62% based on the total weight of the grafted polyvinyl alcohol polymer. 18. The grafted polyvinyl alcohol polymer according to claim 1 , having a solid content of at least 25% solids. 19. The grafted polyvinyl alcohol polymer according to claim 1 in the form of dry solid particulate. 20. A polymer composition comprising: the grafted polyvinyl alcohol polymer according to claim 1 ; and an aqueous medium in which the grafted polyvinyl alcohol polymer is dispersed, and wherein said polymer composition is an emulsion polymer composition. 21. The polymer composition according to claim 20 , which has a pH of from about 3 to about 6. 22. An aqueous based graft emulsion polymer, comprising the grafted polyvinyl alcohol polymer according to claim 1 . 23. The polymer composition of claim 20 , wherein said branched alkyl acylate is present in said polymer composition in an amount of at least 24% by total solid weight. 24. The polymer composition of claim 20 , wherein said branched alkyl acylate is present in said polymer composition in an amount of at least 50% by total solid weight. 25. The polymer composition of claim 20 , wherein said one or more of said side chains from the plurality of side chains comprise one or more units of said aliphatic monocarboxylic acid, said aliphatic dicarboxylic acid, and said reactive quaternary ammonium salt. 26. The polymer composition of claim 20 , wherein said one or more of said side chains from the plurality of side chains comprise one or more units of said aliphatic monocarboxylic acid, said aliphatic dicarboxylic acid, and said reactive quaternary ammonium salt, and further comprise units of an aliphatic amide.

Assignees

Inventors

Classifications

  • Paper recycling · CPC title

  • Working-up waste paper (mechanical part D21B1/08, D21B1/32) · CPC title

  • Polyalkenyalcohols; Polyalkenylethers; Polyalkenylesters · CPC title

  • C08L51/003Primary

    grafted on to macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds (C08L51/04, C08L51/06 take precedence) · CPC title

  • C08F261/04Primary

    on to polymers of vinyl alcohol · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11345807B2 cover?
A grafted polyvinyl alcohol polymer has a balance between hydrophilicity and hydrophobicity. The grafted polyvinyl alcohol polymer has a chemical functionality that allows for adsorption onto the pulp fibers, polymer film formation upon drying, repelling water upon wetting, polymer film swelling and breaking for prolonged wetting by water. When incorporated into paper products, the polymer can …
Who is the assignee on this patent?
Buckman Laboratories Int Inc
What technology area does this patent fall under?
Primary CPC classification C08L51/003. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue May 31 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).