Method of preparing a super absorbent polymer and a super absorbent polymer prepared therefrom
US-2015259522-A1 · Sep 17, 2015 · US
US9975979B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9975979-B2 |
| Application number | US-201515502592-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 8, 2015 |
| Priority date | Oct 8, 2014 |
| Publication date | May 22, 2018 |
| Grant date | May 22, 2018 |
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A method of preparing a superabsorbent polymer is provided. The method of preparing the superabsorbent polymer according to the present disclosure is able to provide the superabsorbent polymer having an improved absorption rate while having superior centrifuge retention capacity (CRC) and absorbency under pressure (AUP).
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The invention claimed is: 1. A method of preparing a superabsorbent polymer, the method comprising: polymerizing and crosslinking a monomer composition having acrylic acid-based monomers having acidic groups which are at least partially neutralized, in the presence of a polymerization initiator and a first crosslinking agent, to form a water-containing gel polymer; coarsely pulverizing the water-containing gel polymer; drying the coarsely pulverized water-containing gel polymer; pulverizing the dried polymer; and surface-modifying the pulverized polymer by a second crosslinking agent, wherein the coarse pulverization of the water-containing gel polymer is conducted while mixing the water-containing gel polymer with a metal sulfate, and a powder of the superabsorbent polymer that is obtained during the preparation process of the superabsorbent polymer, and the powder of the superabsorbent polymer is uniformly distributed on the surface of the coarsely pulverized water-containing gel polymer. 2. The method of preparing the superabsorbent polymer of claim 1 , wherein the powder of the superabsorbent polymer comprises fine particles having a particle size of 10 μm to 150 μm obtained during the preparation process of the superabsorbent polymer, granules of the fine particles, or a mixture of the fine particles and the granules. 3. The method of preparing the superabsorbent polymer of claim 1 , wherein the powder of the superabsorbent polymer is mixed in an amount of 3 parts by weight to 40 parts by weight, based on 100 parts by weight of the water-containing gel polymer. 4. The method of preparing the superabsorbent polymer of claim 1 , wherein the metal sulfate is mixed in an amount of 0.01 parts by weight to 20 parts by weight, based on 100 parts by weight of the water-containing gel polymer. 5. The method of preparing the superabsorbent polymer of claim 1 , wherein the metal sulfate is one or more compounds selected from the group consisting of zinc sulfate, magnesium sulfate, aluminum sulfate, iron sulfate, and zirconium sulfate. 6. The method of preparing the superabsorbent polymer of claim 1 , wherein the coarsely pulverized water-containing gel polymer has an average particle size of 2 mm to 10 mm. 7. The method of preparing the superabsorbent polymer of claim 1 , wherein the acrylic acid-based monomer is a compound represented by the following Chemical Formula 1: R 1 —COOM 1 [Chemical Formula 1] wherein R 1 is an alkyl group having an unsaturated bond and having 2 to 5 carbon atoms, and M 1 is a hydrogen atom, a monovalent metal, a divalent metal, an ammonium group, or an organic amine salt. 8. The method of preparing the superabsorbent polymer of claim 1 , wherein the drying of the coarsely pulverized water-containing gel polymer is performed at a temperature of 120° C. to 250° C. 9. The method of preparing the superabsorbent polymer of claim 1 , wherein the first crosslinking agent is one or more compounds selected from the group consisting of N,N′-methylenebisacrylamide, trimethylolpropane tri(meth)acrylate, ethylene glycol di(meth)acrylate, polyethylene glycol(meth)acrylate, propylene glycol di(meth)acrylate, polypropylene glycol(meth)acrylate, butanediol di(meth)acrylate, butylene glycol di(meth)acrylate, diethylene glycol di(meth)acrylate, hexanediol di(meth)acrylate, triethylene glycol di(meth)acrylate, tripropylene glycol di(meth)acrylate, tetraethylene glycol di(meth)acrylate, dipentaerythritol pentacrylate, glycerin tri(meth)acrylate, pentaerythritol tetraacrylate, triarylamine, ethylene glycol diglycidyl ether, propylene glycol, glycerin, and ethylene carbonate. 10. The method of preparing the superabsorbent polymer of claim 1 , wherein, in the surface modification of the pulverized polymer, a surface crosslinking reaction of the pulverized polymer is performed by mixing the pulverized polymer with 0.001 parts to 5 parts by weight of the second crosslinking agent, based on 100 parts by weight of the pulverized polymer. 11. The method of preparing the superabsorbent polymer 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.
Post-polymerisation treatments (C08F8/00 takes precedence; of conjugated diene rubbers C08C) · CPC title
Homopolymers or copolymers of acids; Metal or ammonium salts thereof · CPC title
Esters · CPC title
Differential crosslinking of one polymer with one crosslinking type, e.g. surface crosslinking · CPC title
Crosslinking, e.g. vulcanising, of macromolecules (mechanical aspects B29C35/00; crosslinking agents C08K) · CPC title
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