Super absorbent polymer and method for preparing the same

Patent metadata

Field	Value
Publication number	US-10450425-B2
Application number	US-201515107297-A
Country	US
Kind code	B2
Filing date	Nov 11, 2015
Priority date	Nov 24, 2014
Publication date	Oct 22, 2019
Grant date	Oct 22, 2019

Abstract

The present invention relates to a super absorbent polymer and a method for preparing the same. The present invention has features that it is possible to prepare a super absorbent resin that can have an improved centrifuge retention capacity (CRC) and a high absorbency under load (AUL) by controlling the shape and size of the chopper die holes during coarse pulverization of a hydrous gel phase polymer.

First claim

The invention claimed is:

1. A method of preparing a superabsorbent polymer comprising:
1) carrying out thermal polymerization or photopolymerization of a monomer composition including a water-soluble ethylene-based unsaturated monomer and a polymerization initiator to form a hydrous gel phase polymer;
2) passing the hydrous gel phase polymer through a chopper die and pulverizing the polymer;
3) drying the pulverized hydrous gel phase polymer;
4) pulverizing the dried polymer; and
5) surface-crosslinking the pulverized polymer,
wherein the chopper die is provided with a plurality of non-circular holes,
the chopper die has an opening/ closing rate of 30 to 40%, and
the chopper die satisfies the following Mathematical Formula 1:
c> 2×√{square root over (0.4×π× n×A )}  [Mathematical Formula 1]

wherein
A is the overall area of the upper surface of the chopper die with a unit mm 2 , n is the number of holes, and c is the total circumference of the plurality of holes, and
wherein the value of c is 500 to 800 mm.

2. The method of claim 1 , wherein the thickness of the chopper die is 5 to 15 mm.

3. The method of claim 1 , wherein the n-holes have the identical shape with each other.

4. The method of claim 1 , wherein n is an integer of 10 to 30.

5. The method of claim 1 , wherein the pulverizing in step 2) is a step of pulverizing the hydrous gel phase polymer into a particle size of 2 to 10 mm.

6. The method of claim 1 , wherein
the drying in step 3) is carried out at a temperature of 120 to 250° C.

7. The method of claim 1 , wherein
the pulverizing in step 4) is carried out so that the particle size of the pulverized polymer becomes 150 to 850 μm.

8. The method of claim 1 , wherein the surface-crosslinking in Step 5) is carried out at a temperature of 100 to 250° C.

9. The method of claim 1 , wherein
the water-soluble ethylene-based unsaturated monomer is a compound represented by the following Chemical Formula 1:
R 1 —COOM 1   [Chemical Formula 1]

in Chemical Formula 1,
R 1 is a C 2 -C 5 alkyl group including an unsaturated bond, and
M 1 is a hydrogen atom, a monovalent or divalent metal, an ammonium group, or an organic amine salt.

10. The method of claim 1 , wherein
the water-soluble ethylene-based unsaturated monomer includes one or more selected from the group consisting of: acrylic acid, methacrylic acid, maleic anhydride, fumaric acid, crotonic acid, itaconic acid, 2-acryloylethane sulfonic acid, 2-methacryloylethane sulfonic acid, 2-(meth)acryloylpropane sulfonic acid, 2-(meth)acrylamide-2-methyl propane sulfonic acid, (meth)acrylamide, N- substituted (meth)acrylate, 2-hydroxyethyl(meth)acrylate, 2-hydroxypropyl(meth)acrylate, methoxy polyethylene glycol (meth)acrylate, polyethylene glycol (meth)acrylate,(N,N)-dimethylaminoethyl(meth)acrylate, and (N,N)-dimethylaminopropyl(meth)acrylamide.

11. The method of claim 1 , wherein
the surface crosslinking is carried out by reacting one or more crosslinking agents selected from the group consisting of ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, glycerol polyglycidyl ether, propylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, ethylene carbonate, ethylene glycol, diethylene glycol, propylene glycol, triethylene glycol, tetraethylene glycol, propanediol, dipropylene glycol, polypropylene glycol, glycerin, polyglycerin, butanediol, heptanediol, hexanediol, trimethylolpropane, pentaerythritol, sorbitol, calcium hydroxide, magnesium hydroxide, aluminum hydroxide, iron hydroxide, calcium chloride, magnesium chloride, aluminum chloride, and iron chloride.

Assignees

• Lg Chemical Ltd

Inventors

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

Classifications

• A61L15/60 Primary

  Liquid-swellable gel-forming materials, e.g. super-absorbents · CPC title

• C08J3/12 Primary

  Powdering or granulating · CPC title

• C08J3/075 Primary

  Macromolecular gels · CPC title

• C08F2810/20

  leading to a crosslinking, either explicitly or inherently · CPC title

• C08K5/053

  Polyhydroxylic alcohols · CPC title