Method for preparing superabsorbent polymer, and superabsorbent polymer prepared thereby

Patent metadata

Field	Value
Publication number	US-11618805-B2
Application number	US-202016871301-A
Country	US
Kind code	B2
Filing date	May 11, 2020
Priority date	Jul 6, 2015
Publication date	Apr 4, 2023
Grant date	Apr 4, 2023

Abstract

The present invention relates to a method for preparing a superabsorbent polymer, and a superabsorbent polymer prepared thereby. A superabsorbent polymer prepared by the preparation method exhibits minimized deterioration of physical properties after being pulverized, and thus basic absorbance performance is excellent and an excellent liquid permeability and absorbance rate can be exhibited.

First claim

The invention claimed is:

1. A superabsorbent polymer comprising a base polymer powder including a crosslinking polymer of water-soluble ethylene-based unsaturated monomers having acidic groups which are at least partially neutralized; and a surface-crosslinked layer formed on the base polymer powder,
wherein the surface-crosslinked layer is obtained by reacting the base polymer powder with a surface crosslinking agent solution comprising a polyvinyl alcohol thickener having a weight average molecular weight of 300 g/mol to 1,000,000 g/mol, an inorganic material, and a surface crosslinking agent, and the polyvinyl alcohol thickener is included in an amount of 0.01 to 1 part by weight with respect to 100 parts by weight of the base polymer powder, and
wherein the superabsorbent polymer has a GBP reduction rate of the following Equation 1 of −55% to 0%:
GBP reduction rate (%)={( G 1 −G 0 )/ G 0 }*100  [Equation 1]

wherein G 0 is an initial gel bed permeability of the superabsorbent polymer, and
G 1 is a gel bed permeability of a superabsorbent polymer having a particle size of 300 μm to 600 μm, which is obtained by pulverizing the superabsorbent polymer using a ball mill under 300 rpm for 20 minutes and then size-sorting the pulverized superabsorbent polymer.

2. The superabsorbent polymer of claim 1 , which has a reduction rate of absorbency under load of the following Equation 2 of −4% to 0%:
Reduction rate of absorbency under load (%)={( A 1 −A 0 )/ A 0 }*100  [Equation 2]

wherein A 0 is an initial absorbency under load of the superabsorbent polymer, on which the surface-crosslinked layer is formed, as calculated by the following Calculation Formula 4, and
A 1 is an absorbency under load of the superabsorbent polymer having a particle size of 300 μm to 600 μm, which is obtained by pulverizing the superabsorbent polymer using a ball mill under 300 rpm for 20 minutes and then size-sorting the pulverized superabsorbent polymer, as calculated by the following Calculation Formula 4,
5 min gel - vac - AUL ( g/g )=[ W 6 ( g )− W 5 ( g )]/ W 0 ( g )  [Calculation Formula 4]

wherein W 0 (g) is an initial weight (g) of the superabsorbent polymer,
W 5 (g) is the sum of the weight of the superabsorbent polymer and a weight of an apparatus capable of providing a load for the superabsorbent polymer, and
W 6 (g) is the sum of the weight of the superabsorbent polymer, which is measured after allowing the superabsorbent polymer to absorb a physiological saline solution under a load (0.3 psi) for 5 minutes and removing residual liquid using a vacuum apparatus, and the weight of the apparatus capable of providing a load for the superabsorbent polymer.

3. The superabsorbent polymer of claim 1 , wherein with regard to the superabsorbent polymer having a particle size of 300 μm to 600 μm, which is obtained by pulverizing the superabsorbent polymer using a ball mill under 300 rpm for 20 minutes and then size-sorting the pulverized superabsorbent polymer, centrifuge retention capacity (CRC) in a physiological saline solution is 30 g/g to 32 g/g, absorbency under load (AUL) of 0.9 psi in the physiological saline solution is 20 to 22 g/g, free swell gel bed permeability (GBP) in the physiological saline solution is 12 darcy to 100 darcy, and absorbency under load (5 min gel-vac-AUL) of the superabsorbent polymer, as measured after swelling the superabsorbent polymer in the physiological saline solution under a load of 0.3 psi for 5 minutes and removing residual liquid under vacuum, is 17 g/g to 19 g/g.

4. The superabsorbent polymer of claim 1 , wherein the inorganic material is included in an amount of more than 0 part by weight to 0.07 parts by weight with respect to 100 parts by weight of the base polymer powder.

5. The superabsorbent polymer of claim 1 , wherein the surface crosslinking agent is one or more polyols selected from the group consisting of ethylene glycol, propylene glycol, 1,4-butanediol, 1,6-hexanediol, 1,2-hexanediol, 1,3-hexanediol, 2-methyl-1,3-propanediol, 2,5-hexanediol, 2-methyl-1,3-pentanediol, 2-methyl-2,4-pentanediol, tripropylene glycol, and glycerol; or one or more carbonate-based compounds selected from the group consisting of ethylene carbonate and propylene carbonate.

6. The superabsorbent polymer of claim 1 , wherein the surface crosslinking agent is included in an amount of 0.01 to 4 parts by weight with respect to 100 parts by weight of the base polymer powder.

Assignees

• Lg Chemical Ltd

Inventors

• Nam Hye Mi
• Hwang Min Ho
• Lee Sang Gi
• Jang Tae Hwan
• Lee Soo Jin

Classifications

• C08L1/02

  Cellulose; Modified cellulose · CPC title

• C08J3/24

  Crosslinking, e.g. vulcanising, of macromolecules (mechanical aspects B29C35/00; crosslinking agents C08K) · CPC title

• C08K5/00

  Use of organic ingredients · CPC title

• C08J2333/02

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

• C08J3/075 Primary

  Macromolecular gels · CPC title