Super absorbent polymer and a preparation method thereof
US-10086361-B2 · Oct 2, 2018 · US
US10857044B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10857044-B2 |
| Application number | US-201615752783-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 29, 2016 |
| Priority date | Jan 28, 2016 |
| Publication date | Dec 8, 2020 |
| Grant date | Dec 8, 2020 |
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The present invention relates to a method for a superabsorbent polymer. The preparation method controls the time from the addition of a foaming agent to the initiation of a polymerization reaction, thereby forming an appropriate pore structure in a superabsorbent polymer. The superabsorbent polymer produced through the preparation method can exhibit a remarkably improved absorption rate while exhibiting excellent absorption performance.
Opening claim text (preview).
The invention claimed is: 1. A method for preparing a superabsorbent polymer comprising: irradiating light within 9 seconds from the moment when a water-soluble ethylenically unsaturated monomer having at least partially neutralized acidic groups makes contact with a foaming agent, and performing crosslinking polymerization via light irradiation of a monomer mixture containing the water-soluble ethylenically unsaturated monomer having at least partially neutralized acidic groups, and the foaming agent, in the presence of an internal crosslinking agent to prepare a hydrogel polymer; drying, pulverizing, and classifying the hydrogel polymer to form a base polymer powder; and additionally crosslinking a surface of the base polymer powder in the presence of a surface crosslinking agent to form a surface-crosslinked layer, wherein the superabsorbent polymer has a centrifuge retention capacity (CRC) for a physiological saline solution of 29 to 33 g/g and absorbency under load (AUL) of under 0.9 psi for a physiological saline solution of 14 to 22 g/g, and a vortex time of 20 to 40 seconds. 2. The method for preparing a superabsorbent polymer of claim 1 , wherein the monomer mixture further contains, as a foam stabilizer, an alkyl sulfate salt, an alkyl sulfonate salt, an alkyl phosphate salt, an alkyl carbonate salt, a polyethylene glycol alkyl ester, a polypropylene glycol alkyl ester, a glucoside alkyl ester, a glycerol alkyl ester, a block-copolymer of polyethylene glycol and polypropylene glycol, or a mixture thereof. 3. The method for preparing a superabsorbent polymer of claim 1 , wherein in the preparing a hydrogel polymer, the foaming agent is added to the monomer mixture in a solid or liquid state without dilution, the foaming agent is added in a solution state after being diluted in a solvent and, the foaming agent is added by spraying, or the forming agent is added by spraying it on a coating film obtained by coating the monomer mixture. 4. The method for preparing a superabsorbent polymer of claim 1 , wherein the foaming agent is at least one carbonate selected from the group consisting of sodium hydrogencarbonate, sodium carbonate, potassium hydrogencarbonate, and potassium carbonate. 5. The method for preparing a superabsorbent polymer of claim 1 , wherein the foaming agent is added in an amount of 0.001 to 1% by weight based on the total amount of the monomer mixture. 6. The method for preparing a superabsorbent polymer of claim 1 , wherein the irradiating light is performed within 5 seconds from the moment when the water-soluble ethylenically unsaturated monomer having at least partially neutralized acidic groups makes contact with the foaming agent. 7. The method for preparing a superabsorbent polymer of claim 1 , wherein the internal crosslinking agent is at least one selected from the group consisting of polyethylene glycol diacrylate, glycerin diacrylate, glycerin triacrylate, unmodified or ethoxylated trimethylolpropane triacrylate, hexanediol diacrylate, and triethylene glycol diacrylate. 8. The method for preparing a superabsorbent polymer of claim 1 , wherein the surface crosslinking agent is at least one polyol selected from the group consisting of ethylene glycol, propylene glycol, 1,4-butanediol, 1,6-hexanediol, 1,2-hexanediol, 1,3-hexanediol, 2-methyl-1,3-propanediol, 2,5-hexanediol, 2-methyl-1,3-pentanediol, 2-methyl-2,4-pentanediol, tripropylene glycol, and glycerol, or at least one carbonate compound selected from the group consisting of ethylene carbonate and propylene carbonate.
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