Superabsorbent polymer having high absorption rate under load and preparation method thereof

Patent metadata

Field	Value
Publication number	US-2018178193-A1
Application number	US-201815903179-A
Country	US
Kind code	A1
Filing date	Feb 23, 2018
Priority date	Nov 27, 2014
Publication date	Jun 28, 2018
Grant date	—

Abstract

Provided are a superabsorbent polymer and a preparation method thereof. In the superabsorbent polymer according to the present invention, a low-temperature foaming agent are used together with a high-temperature foaming agent to control the size and distribution of internal pores of the superabsorbent polymer, thereby increasing absorption rate under load without reduction in gel strength.

First claim

1 . A method of preparing a superabsorbent polymer comprising:
1) polymerizing or crosslinking a monomer composition comprising acrylic acid-based monomers having acidic groups which are at least partially neutralized, in the presence of a polymerization initiator, a first crosslinking agent, a low-temperature foaming agent, and a high-temperature foaming agent at 25 to 100° C. to form a water-containing gel polymer, 2) coarsely pulverizing the water-containing gel polymer, 3) drying the coarsely pulverized water-containing gel polymer at 150° C. to 250° C., 4) pulverizing the dried polymer, and 5) surface-modifying the pulverized polymer by a second crosslinking agent.

2 . The method of claim 1 , wherein a weight ratio of the low-temperature foaming agent and the high-temperature foaming agent is 50:1 to 2:1.

3 . The method of claim 1 , wherein the low-temperature foaming agent is sodium bicarbonate, sodium carbonate, potassium bicarbonate, potassium carbonate, calcium bicarbonate, calcium carbonate, magnesium bicarbonate, or magnesium carbonate.

4 . The method of claim 1 , wherein the polymerization and crosslinking of step 1 are performed at a temperature of 30° C. to 90° C.

5 . The method of claim 1 , wherein the high-temperature foaming agent is azodicarbonamide (ADCA), dinitroso pentamethylene tetramine (DPT), p,p′-oxybisbenzenesulfonylhydrazide (OBSH), p-toluenesulfonyl hydrazide (TSH), or sugar ester.

6 . The method of claim 5 , wherein the sugar ester is sucrose stearate, sucrose palmitate, or sucrose laurate.

7 . The method of claim 1 , wherein the drying of step 3 is performed at a temperature of 150° C. to 200° C.

8 . The method of claim 1 , wherein the second crosslinking agent is one or more compounds 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 glycol, diethylene glycol, propylene glycol, triethylene glycol, tetraethylene glycol, propane diol, dipropylene glycol, polypropylene glycol, glycerin, polyglycerin, butanediol, heptanediol, hexanediol, trimethylol propane, pentaerythritol, sorbitol, calcium hydroxide, magnesium hydroxide, aluminum hydroxide, iron hydroxide, calcium chloride, magnesium chloride, aluminum chloride, and iron chloride.

Assignees

• Lg Chemical Ltd

Inventors

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

Classifications

• C08F20/10 Primary

  Esters · CPC title

• B01J20/267 Primary

  Cross-linked polymers · CPC title

• C08J2205/048

  Bimodal pore distribution, e.g. micropores and nanopores coexisting in the same foam · CPC title

• C08J9/08

  developing carbon dioxide · CPC title

• B01J20/3085

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