Water-absorbent resin composition, absorbent material and absorbent article
US-2024424473-A1 · Dec 26, 2024 · US
US2016361703A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016361703-A1 |
| Application number | US-201515104485-A |
| Country | US |
| Kind code | A1 |
| Filing date | Nov 24, 2015 |
| Priority date | Dec 22, 2014 |
| Publication date | Dec 15, 2016 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Provided are a superabsorbent polymer and a preparation method thereof. The superabsorbent polymer according to the present invention has excellent gel bed permeability (GBP) and suction power, thereby being usefully applied to hygiene products such as diapers.
Opening claim text (preview).
1 . A super absorbent polymer, comprising a base polymer comprising a crosslinked polymer of water-soluble ethylene-based unsaturated monomers having acidic groups which are at least partially neutralized, and a surface crosslinked layer comprising the additionally crosslinked polymer of the base polymer, which is formed on the base polymer, wherein suction power of 1 g of the superabsorbent polymer for 5 minutes is 13 mL/g or more and gel bed permeability (GBP) of the superabsorbent polymer is 41 Darcy or more. 2 . The super absorbent polymer of claim 1 , wherein absorbency under load (AUL) at 0.9 psi of the superabsorbent polymer is 17.3 g/g or more. 3 . The super absorbent polymer 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] wherein, R 1 is an alkyl group containing an unsaturated bond and having 2 to 5 carbon atoms, and M 1 is a hydrogen atom, a monovalent or divalent metal, an ammonium group, or an organic amine salt. 4 . The super absorbent polymer of claim 1 , wherein the water-soluble ethylene-based unsaturated monomer comprises one or more selected from the group consisting of an anionic monomer such as acrylic acid, (meth)acrylic acid, maleic anhydride, fumaric acid, crotonic acid, itaconic acid, 2-acryloylethane sulfonic acid, 2-methacryloylethane sulfonic acid, 2-(meth)acryloylpropane sulfonic acid, or 2-(meth)acrylamide-2-methyl propane sulfonic acid, and salts thereof; a nonionic hydrophilic monomer such as (meth)acrylamide, N-substituted (meth)acrylate, 2-hydroxyethyl(meth)acrylate, 2-hydroxypropyl(meth)acrylate, methoxy polyethylene glycol (meth)acrylate, or polyethylene glycol (meth)acrylate; and an amino group-containing unsaturated monomer such as (N,N)-dimethylaminoethyl(meth)acrylate or (N,N)-dimethylaminopropyl(meth)acrylamide, and a quaternary compound thereof. 5 . A method of preparing the superabsorbent polymer of claim 1 , the method comprising the steps of: 1) performing thermal polymerization or photo-polymerization of a monomer composition comprising water-soluble ethylene-based unsaturated monomers and a polymerization initiator to form a water-containing gel polymer, 2) drying the water-containing gel polymer, 3) pulverizing the dried polymer, and 4) surface-crosslinking the pulverized polymer by reacting the pulverized polymer with a compound having two or more epoxy rings at 170 to 250° C. for 50 minutes or longer. 6 . The method of claim 5 , wherein Step 1 is performed in the presence of one or more internal crosslinking agents selected from the group consisting of polyethylene glycol diacrylate (PEGDA), glycerin diacrylate, glycerin triacrylate, non-modified or ethoxylated trimethylol propane triacrylate (TMPTA), hexanediol diacrylate, and triethylene glycol diacrylate. 7 . The method of claim 5 , further comprising the step of pulverizing the water-containing gel polymer to a particle diameter of 2 to 10 mm before drying of the water-containing gel polymer. 8 . The method of claim 5 , wherein pulverization of the dried polymer is performed to make the pulverized polymer have a particle diameter of 150 to 850 μm. 9 . The method of claim 5 , wherein the compound having two or more epoxy rings is a compound represented by the following Chemical Formula 2: wherein, R 2 is C 1-3 alkylene. 10 . The method of claim 5 , wherein the surface crosslinking reaction is performed by using silica. 11 . The method of claim 5 , wherein the surface crosslinking reaction is performed by using silica or polyol. 12 . The method of claim 11 , wherein the polyol is ethylene glycol, diethylene glycol, propylene glycol, triethylene glycol, tetraethylene glycol, propane diol, dipropylene glycol, polypropylene glycol, glycerin, polyglycerin, butanediol, heptanediol, hexanediol, trimethylol propane, pentaerythritol, or sorbitol.
Macromolecular gels · CPC title
Homopolymers or copolymers of acids; Metal or ammonium salts thereof · CPC title
Liquid-swellable gel-forming materials, e.g. super-absorbents · CPC title
Crosslinking, e.g. vulcanising, of macromolecules (mechanical aspects B29C35/00; crosslinking agents C08K) · CPC title
Differential crosslinking of one polymer with one crosslinking type, e.g. surface crosslinking · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.