IP Library Granted Patent US 11,613,613
Granted Patent B2
US 11,613,613 · App. 16/770,414 · Granted Mar 28, 2023

Superabsorbent polymer composition and method for preparing the same

Inventors: Bohee Park (Daejeon, KR); Dae Woo Nam (Daejeon, KR); Young Jae Hur (Daejeon, KR); Yeon Woo Hong (Daejeon, KR); Jiyoon Jeong (Daejeon, KR)
C08J3/245C08L71/02C08F20/06C08J2333/08C08K3/011C08K5/0025C08L33/02C08L2205/03C08L2312/00
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Quick Facts
Patent No.
US 11,613,613
App. No.
16/770,414
Granted
Mar 28, 2023
Kind
B2
Abstract

The present invention relates to superabsorbent polymer and a method for preparing the same. The present invention can provide a superabsorbent polymer in which a hydrophobic material having an HLB of 0-6, a hydrophilic polymer and a surface cross-linking agent are mixed into a base resin, thereby having improved rewetting characteristics and permeability through surface-modification of the base resin.

Claims (36)

1. A method for preparing superabsorbent polymer comprising:

preparing a base resin in which acrylic acid-based monomers having acid groups, of which at least a part are neutralized, and an internal crosslinking agent are crosslinked;

mixing a hydrophobic material having a HLB of 0 or more and 6 or less, a hydrophilic polymer, and a surface crosslinking agent with the base resin to obtain a mixture; and

increasing a temperature of the mixture to conduct surface modification of the base resin,

wherein the hydrophilic polymer includes one or more of dextrine-based compounds, cellulose-based compounds, polyvinylalcohol-based compounds, or polyethyleneglycol-based compounds.

2. The method for preparing superabsorbent polymer according to claim 1 , wherein during the mixing, the hydrophobic material is dry mixed with the base resin, and then, the surface crosslinking agent and the hydrophilic polymer are mixed.

3. The method for preparing superabsorbent polymer according to claim 2 , wherein the surface crosslinking agent and the hydrophilic polymer are dissolved in water and mixed in a state of a surface crosslinking solution.

4. The method for preparing superabsorbent polymer according to claim 1 , wherein the hydrophobic material has a melting point below the increased temperature.

5. The method for preparing superabsorbent polymer according to claim 1 , wherein the hydrophobic material includes one or more of glyceryl stearate, glycol stearate, magnesium stearate, glyceryl laurate, sorbitan stearate, sorbitan trioleate, or PEG-4 dilaurate.

6. The method for preparing superabsorbent polymer according to claim 1 , wherein the hydrophilic polymer has the HLB of 8 or more.

7. The method for preparing superabsorbent polymer according to claim 1 , wherein the hydrophobic material is glyceryl stearate, and the hydrophilic polymer is polyethylene glycol.

8. The method for preparing superabsorbent polymer according to claim 1 , wherein the hydrophobic material is mixed in a content of 0.02 to 0.5 parts by weight, based on 100 parts by weight of the base resin.

9. The method for preparing superabsorbent polymer according to claim 1 , wherein the hydrophilic polymer is mixed in a content of 0.001 to 0.5 parts by weight, based on 100 parts by weight of the base resin.

10. The method for preparing superabsorbent polymer according to claim 1 , wherein the temperature is increased to 90 to 190° C.

11. The method for preparing superabsorbent polymer according to claim 1 , wherein the preparing the base resin comprises:

polymerizing a monomer composition comprising acrylic acid-based monomers having acid groups, of which at least a part are neutralized, an internal crosslinking agent, and a polymerization initiator to form a hydrogel polymer;

drying the hydrogel polymer;

grinding the dried polymer; and

sieving the ground polymer.

12. The method for preparing superabsorbent polymer according to claim 1 , wherein the superabsorbent polymer has a permeability (unit: seconds) measured according to the following Equation 1, of 30 seconds or less:

Permeability(sec)= T 1− B   [Equation 1]

wherein in the Equation 1,

T1 is a time taken until the height of a liquid level decreases from 40 ml to 20 ml, after putting 0.2±0.0005 g of a sieved (30#˜50#) superabsorbent polymer sample in a chromatography column and adding brine to the volume of 50 ml, and then, leaving it for 30 minutes; and B is a time taken until the height of a liquid level decreases from 40 ml to 20 ml in a chromatography column filled with brine.

13. A superabsorbent polymer comprising:

a base resin comprising a crosslinked polymer in which acrylic acid-based monomers having acid groups, of which at least a part are neutralized, are crosslinked; and

a surface modification layer formed on a surface of base resin particles, in which the crosslinked polymer is additionally crosslinked by a surface crosslinking agent,

wherein the surface modification layer comprises a hydrophobic material having a HLB of 0 or more and 6 or less, and a hydrophilic polymer, and

a permeability (unit: seconds) measured according to the following Equation 1 is 30 seconds or less:

Permeability(sec)= T 1− B   [Equation 1]

wherein in the Equation 1,

T1 is a time taken until the height of a liquid level decreases from 40 ml to 20 ml, after putting 0.2±0.0005 g of a sieved (30#˜50#) superabsorbent polymer sample in a chromatography column and adding brine to the volume of 50 ml, and then, leaving it for 30 minutes; and B is a time taken until the height of a liquid level decreases from 40 ml to 20 ml in a chromatography column filled with brine.

14. The superabsorbent polymer according to claim 13 , wherein the hydrophobic material includes one or more of glyceryl stearate, glycol stearate, magnesium stearate, glyceryl laurate, sorbitan stearate, sorbitan trioleate, or PEG-4 dilaurate.

15. The superabsorbent polymer according to claim 13 , wherein the superabsorbent polymer has a rewet property (tap water short-term rewet under no pressure) of 2.0 g or less, said rewet property being defined by a weight of water exuding from the superabsorbent polymer to a filter paper, after 1 g of the superabsorbent polymer is soaked in 100 g of tap water to swell for 10 minutes to produce a swollen superabsorbent polymer, and then, the swollen superabsorbent polymer is left on the filter paper for 1 hour from a first time point when it is soaked in the tap water.

16. The superabsorbent polymer according to claim 13 , wherein the superabsorbent polymer has a rewet property (tap water rewet under pressure) of 1.5 g or less, said rewet property being defined by a weight of water exuding from the superabsorbent polymer to a filter paper, after 4 g of the superabsorbent polymer is soaked in 200 g of tap water to swell for 6 hours to produce a swollen superabsorbent polymer, and then, the swollen superabsorbent polymer is left on the filter paper for 1 minute under pressure of 0.75 psi.

17. The superabsorbent polymer according to claim 13 , wherein the superabsorbent polymer has a rewet property (brine rewet under pressure) of 5.0 g or less, said rewet property being defined by a weight of brine exuding from the superabsorbent polymer to a filter paper, after 4 g of the superabsorbent polymer is soaked in 100 g of brine to swell for 2 hours to produce a swollen superabsorbent polymer, and then, the swollen superabsorbent polymer is left on the filter paper for 1 minute under pressure of 0.75 psi.

18. The superabsorbent polymer according to claim 13 , wherein the hydrophobic material is included in a content of 0.02 to 0.5 parts by weight, based on 100 parts by weight of the base resin.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 9, 2020
From: PARK, BOHEE; NAM, DAE WOO; HUR, YOUNG JAE; HONG, YEON WOO; JEONG, JIYOON
To: LG CHEM, LTD.
Reel/Frame 052880/0454 →
Priority Claims (2)
KR 10-2017-0169497 · Dec 11, 2017 · national
KR 10-2018-0148842 · Nov 27, 2018 · national
Continuity (1)
Related Publication 20200308352A1 · Oct 1, 2020