Method for preparing superabsorbent polymer and superabsorbent polymer prepared thereby

Patent metadata

Field	Value
Publication number	US-11071968-B2
Application number	US-202016809057-A
Country	US
Kind code	B2
Filing date	Mar 4, 2020
Priority date	Mar 24, 2016
Publication date	Jul 27, 2021
Grant date	Jul 27, 2021

Abstract

The present invention relates to a method for preparing superabsorbent polymer that has not only excellent permeability and absorption speed, but also minimized absorbency under pressure decrease rate, and superabsorbent polymer prepared thereby.

First claim

The invention claimed is:

1. A method for preparing superabsorbent polymer comprising the steps of:
(a) polymerizing a monomer mixture in the presence of an internal crosslinking agent to form a hydrogel polymer, wherein the monomer mixture comprises a water soluble ethylenically unsaturated monomer having an acid group of which at least a part is neutralized;
(b) drying, grinding and sieving the hydrogel polymer to form a base resin powder;
(c) surface crosslinking the base resin powder in the presence of a surface crosslinking solution to form a surface crosslinked layer on the base resin powder, wherein the surface crosslinking solution comprises a first inorganic material; and
(d) adding a second inorganic material on a surface of the surface crosslinked layer to form a superabsorbent polymer,
wherein the second inorganic material comprises alumina having a BET specific surface area of 50 m 2 /g to 200 m 2 /g,
wherein the second inorganic material is present between 0.01 parts by weight to 0.2 parts by weight, based on 100 parts by weight of the base resin powder,
wherein the second inorganic material is present between 10 parts by weight to 200 parts by weight, based on 100 parts by weight of the first inorganic material,
wherein the first inorganic material is different from the second inorganic material, and
wherein the superabsorbent polymer has absorbency under a load decrease rate of −15% to −2.8%, as measured at 0.9 psi according to the following Equation 3:
Decrease rate of absorbency under load of 0.9 psi (%)={( A 3− A 2)/ A 2}*100  [Equation 3]

in the Equation 3,

A2 is absorbency under a load value of superabsorbent polymer that does not comprise the first inorganic material and the second inorganic material, calculated by the following Equation 4,
A3 is absorbency under a load value of superabsorbent polymer that comprises the first inorganic material and the second inorganic material, calculated by the following Equation 4,
AUL(g/g) of 0.9 psi=[ W 4 (g)− W 3 (g)]/ W 0 (g)  [Equation 4]

in the Equation 4,
W 0 (g) is an initial weight of superabsorbent polymer(g), W 3 (g) is a sum of a weight of the superabsorbent polymer and a weight of a device capable of giving a load to the superabsorbent polymer, W 4 (g) is a sum of a weight of the superabsorbent polymer and a weight of the device capable of giving a load to the superabsorbent polymer, after absorbing a saline solution into the superabsorbent polymer under a load of 0.9 psi for 1 hour.

2. The method for preparing the superabsorbent polymer according to claim 1 , wherein the first inorganic material included in the surface crosslinked layer contacts the surface of the base resin powder.

3. The method for preparing the superabsorbent polymer according to claim 1 , wherein in step (c) a content of the first inorganic material is 0.001 parts by weight to 1 part by weight, based on 100 parts by weight of the base resin powder.

4. The method for preparing the superabsorbent polymer according to claim 1 , wherein in step (d) a content of the second inorganic material is 0.001 parts by weight to 1 part by weight, based on 100 parts by weight of the base resin powder.

5. The method for preparing the superabsorbent polymer according to claim 1 , wherein the first inorganic material comprises one or more selected from the group consisting of silica, clay, alumina, silica-alumina composite, titania, zinc oxide, and aluminum sulfate.

6. The method for preparing the superabsorbent polymer according to claim 1 , wherein a particle diameter of alumina is 1 nm to 100 nm.

7. The method for preparing the superabsorbent polymer according to claim 5 , wherein the alumina has a BET specific surface area of 50 m 2 /g to 200 m 2 /g.

8. The method for preparing the superabsorbent polymer according to claim 1 , wherein a surface of silica or a surface of alumina is positively charged.

9. The method for preparing the superabsorbent polymer according to claim 1 , wherein the surface crosslinking agent includes one or more polyols selected from the group consisting of ethyleneglycol, propyleneglycol, 1,4-butandiol, 1,6-hexandiol, 1,2-hexandiol, 1,3-hexandiol, 2-methyl-1,3-propandiol, 2,5-hexandiol, 2-methyl-1,3-pentandiol, 2-methyl-2,4-pentandiol, tripropyleneglycol and glycerol; or one or more carbonate-based compounds selected from the group consisting of ethylene carbonate and propylene carbonate.

10. The method for preparing the superabsorbent polymer according to claim 1 , wherein the surface crosslinking solution further comprises one or more kinds of solvents selected from the group consisting of water, ethanol, ethyleneglycol, diethyleneglycol, triethyleneglycol, 1,4-butandiol, propyleneglycol, ethyleneglycol monobutylether, propyleneglycol monomethylether, propyleneglycol monomethyl ether acetate, methyl ethyl ketone, acetone, methyl amyl ketone, cyclohexanone, cyclopentanone, diethyleneglycol monomethyl ether, diethyleneglycol ethyl ether, toluene, xylene, butyrolactone, carbitol, methyl cellosolve acetate and N,N-dimethylacetamide.

11. The method for preparing the superabsorbent polymer according to claim 1 , further comprising:
(e) crushing the superabsorbent polymer.

12. A method for preparing superabsorbent polymer comprising the steps of:
(a) polymerizing a monomer mixture in the presence of an internal crosslinking agent to form a hydrogel polymer, wherein the monomer mixture comprises a water soluble ethylenically unsaturated monomer having an acid group of which at least a part is neutralized;
(b) drying, grinding and sieving the hydrogel polymer to form a base resin powder;
(c) surface crosslinking the base resin powder in the presence of a surface crosslinking solution to form a surface crosslinked layer on the base resin powder, wherein the surface crosslinking solution comprises a first inorganic material; and
(d) adding a second inorganic material on a surface of the surface crosslinked layer to form a superabsorbent polymer,
wherein the second inorganic material comprises alumina having a BET specific surface area of 50 m 2 /g to 200 m 2 /g,
wherein the second inorganic material is present between 0.01 parts by weight to 0.2 parts by weight, based on 100 parts by weight of the base resin powder,
wherein the second inorganic material is present between 700 parts by weight to 1500 parts by weight, based on 100 parts by weight of the first inorganic material,
wherein the first inorganic material is different from the second inorganic material, and
wherein an anti-caking efficiency of the superabsorbent polymer according to the following Equation 5 is 95% to 100%,
Anti-caking efficiency (%)=[ W 6 (g)/ W 5 (g)]*100  [Equation 5]

in the Equation 5,

W 5 (g) is an initial weight of the superabsorbent polymer(g), and W 6 (g) is an amount(g) of the superabsorbent polymer dropped when the superabsorbent polymer is applied on a flask dish of 9 cm diameter, maintained in a constant temperature and humidity chamber of temperature of 40±3° C. and humidity of 80±3% for 10 minutes, and cooled at room temperature for 5 minutes, and then, the flask dish is turned upside down on a filter paper.

Assignees

• Lg Chemical Ltd

Inventors

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

Classifications

• C08J3/075

  Macromolecular gels · CPC title

• C08J3/245 Primary

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

• C08J3/24

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

• C08J2333/02

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

• B01J20/28059

  being less than 100 m2/g · CPC title