Superabsorbent polymer and preparation method thereof

US12343701B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12343701-B2
Application numberUS-202017441994-A
CountryUS
Kind codeB2
Filing dateSep 7, 2020
Priority dateSep 30, 2019
Publication dateJul 1, 2025
Grant dateJul 1, 2025

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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Abstract

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Provided are a superabsorbent polymer capable of exhibiting improved bacterial growth-inhibitory property without deterioration in physical properties of the superabsorbent polymer, such as water retention capacity and absorbency under pressure, or without an increase in the generation of dust, and a preparation method thereof. The superabsorbent polymer may include a base polymer powder including a crosslinked polymer of water-soluble ethylenically unsaturated monomers including acidic groups, of which at least a part is neutralized; and a surface-crosslinked layer which is obtained by additionally crosslinking the crosslinked polymer via a surface crosslinking agent to be formed on the surface of the base polymer powder, wherein the crosslinked polymer of the base polymer powder or the surface-crosslinked layer includes an antimicrobial agent including an organic acid salt having an aromatic ring inside the crosslinked structure thereof.

First claim

Opening claim text (preview).

The invention claimed is: 1. A superabsorbent polymer comprising: a base polymer powder including a crosslinked polymer of water-soluble ethylenically unsaturated monomers including acidic groups, of which at least a part is neutralized; and a surface-crosslinked layer formed on the surface of the base polymer powder by additionally crosslinking the crosslinked polymer via a surface crosslinking agent, wherein the crosslinked polymer of the base polymer powder includes an antimicrobial agent including an organic acid salt having an aromatic ring inside a crosslinked structure thereof, wherein the organic acid salt having an aromatic ring is included in an amount of 0.1 part by weight to 5 parts by weight, based on 100 parts by weight of the base polymer powder. 2. The superabsorbent polymer of claim 1 , wherein the organic acid salt having an aromatic ring is a sodium (Na) salt or a zinc (Zn) salt of an organic acid having an aromatic ring. 3. The superabsorbent polymer of claim 1 , wherein the organic acid salt having an aromatic ring is sodium benzoate or zinc benzoate. 4. The superabsorbent polymer of claim 1 , wherein the antimicrobial agent further includes ethylenediaminetetraacetic acid (EDTA) or an alkali metal salt thereof. 5. The superabsorbent polymer of claim 4 , wherein the EDTA or alkali metal salt thereof is included in an amount of 0.1 part by weight to 3 parts by weight, based on 100 parts by weight of the base polymer powder. 6. The superabsorbent polymer of claim 1 , wherein the surface crosslinking agent includes a diol compound, an alkylene carbonate compound, or a polyvalent epoxy compound. 7. The superabsorbent polymer of claim 1 , wherein the superabsorbent polymer has a bacterial inhibition rate ( Escherichia Coli ; ATCC25922) of 75% or more, represented by the following Equation 1: Bacterial inhibition rate=[1−{CFU(12 h)/CFUcontrol (12 h)}]*100(%)  [Equation 1] in Equation 1, CFU (12 h) represents a number of individuals of proliferated bacteria per unit volume of synthetic urine (CFU/ml), which was obtained by adding the superabsorbent polymer to synthetic urine inoculated with bacteria of Escherichia Coli (ATCC 25922), and then incubating for 12 hours at 35° C., and CFUcontrol (12 h) represents a number of individuals of proliferated bacteria per unit volume of synthetic urine (CFU/ml), which was obtained by incubating synthetic urine inoculated with bacteria of Escherichia Coli (ATCC 25922), without the superabsorbent polymer, under the same conditions. 8. The superabsorbent polymer of claim 1 , wherein the superabsorbent polymer has a dust number of 1 to 5, as calculated according to the following Equation 2 from results of a laser dust meter: Dust number=Max value+30 sec. value  [Equation 2] in Equation 2, Max value represents a value which is measured at a maximum DUST value when the superabsorbent polymer is dropped into an inlet of the laser dust meter, and 30 sec. value represents a value which is measured for 30 seconds after the Max value is displayed. 9. A method of preparing the superabsorbent polymer of claim 1 , the method comprising: performing crosslinking polymerization of water-soluble ethylenically unsaturated monomers including acidic groups, of which at least a part is neutralized, in the presence of an internal crosslinking agent to form a water-containing gel polymer; drying, pulverizing, and size-sorting the water-containing gel polymer to form a base polymer powder; and performing additional crosslinking of the base polymer powder by heat treatment in the presence of a surface crosslinking agent, wherein the forming the water-containing gel polymer or the performing additional crosslinking is performed in the presence of an antimicrobial agent containing an organic acid salt having an aromatic ring. 10. The method of claim 9 , wherein, during the forming the water-containing gel polymer, crosslinking polymerization of a monomer aqueous solution including the water-soluble ethylenically unsaturated monomers, a polymerization initiator, the internal crosslinking agent, and the antimicrobial agent is performed. 11. The method of claim 9 , wherein the performing additional crosslinking is performed by using a surface crosslinking solution including the surface crosslinking agent and the antimicrobial agent. 12. The method of claim 9 , wherein the organic acid salt having an aromatic ring is included in an amount of 0.1 part by weight to 5 parts by weight, based on 100 parts by weight of the water-soluble ethylenically unsaturated monomers or the base polymer powder. 13. The method of claim 9 , wherein the antimicrobial agent further includes EDTA or an alkali metal salt thereof. 14. The method of claim 13 , wherein the EDTA or alkali metal salt thereof is used in an amount of 0.1 part by weight to 3 parts by weight, based on 100 parts by weight of the water-soluble ethylenically unsaturated monomers or the base polymer powder. 15. A hygienic product comprising the superabsorbent polymer of claim 1 .

Assignees

Inventors

Classifications

  • Homopolymers or copolymers of acids; Metal or ammonium salts thereof · CPC title

  • C08J3/245Primary

    Differential crosslinking of one polymer with one crosslinking type, e.g. surface crosslinking · CPC title

  • Powdering or granulating · CPC title

  • Materials comprising a mixture of organic materials (materials coated or impregnated on a carrier B01J20/32) · CPC title

  • Chemical treatments not covered by groups B01J20/3007 - B01J20/3078 · CPC title

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What does patent US12343701B2 cover?
Provided are a superabsorbent polymer capable of exhibiting improved bacterial growth-inhibitory property without deterioration in physical properties of the superabsorbent polymer, such as water retention capacity and absorbency under pressure, or without an increase in the generation of dust, and a preparation method thereof. The superabsorbent polymer may include a base polymer powder includ…
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification C08J3/245. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 01 2025 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 5 related publications on this page (citations in our corpus or others sharing the same primary CPC).