Novel bifunctional (meth)acrylate compound and polymer
US-2020392065-A1 · Dec 17, 2020 · US
US11970443B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11970443-B2 |
| Application number | US-201916966324-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 18, 2019 |
| Priority date | Oct 18, 2018 |
| Publication date | Apr 30, 2024 |
| Grant date | Apr 30, 2024 |
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 novel crosslinking agent compound, and a superabsorbent polymer prepared by using the same. More particularly, provided are a crosslinking agent compound having a novel structure, which exhibits excellent crosslinking property and thermal degradability, and a superabsorbent polymer prepared by using the same.
Opening claim text (preview).
The invention claimed is: 1. A composition comprising a crosslinking agent compound represented by Chemical Formula 1, and an acrylic acid-based monomer: in Chemical Formula 1, R 1 and R 2 are each independently hydrogen or methyl, R 3 and R 4 are each independently alkyl having 1 to 20 carbon atoms, R 5 and R 6 are each independently hydrogen, alkyl having 1 to 20 carbon atoms, or cycloalkyl having 3 to 20 carbon atoms, or R 5 and R 6 are connected to each other to form a divalent aliphatic ring, and n is an integer of 0 to 10. 2. The composition of claim 1 , wherein R 1 and R 2 are hydrogen. 3. The composition of claim 1 , wherein R 3 and R 4 are each independently alkyl having 1 to 20 carbon atoms, and R 5 and R 6 are each independently hydrogen, alkyl having 1 to 5 carbon atoms, or divalent form of cycloalkane formed by connecting two or more groups adjacent to each other. 4. The composition of claim 3 , wherein R 3 and R 4 are each independently methyl, or ethyl, and R 5 and R 6 are each independently hydrogen, methyl, or ethyl. 5. The composition of claim 1 , wherein n is an integer of 0 to 5. 6. The composition crosslinking agent compound of claim 1 , wherein Chemical Formula 1 is selected from compounds represented by the following Chemical Formulae 1-1 to 1-3: 7. A superabsorbent polymer comprising a polymer which is obtained by polymerizing the composition of claim 1 , wherein the polymer comprises a thermally degradable internal crosslinked structure. 8. The superabsorbent polymer of claim 7 , wherein the acrylic acid-based monomer is represented by the following Chemical Formula 2: R-COOM [Chemical Formula 2] in Chemical Formula 1, R is an alkyl group containing an unsaturated bond and having 2 to 5 carbon atoms, and M is a hydrogen atom, a monovalent or divalent metal, an ammonium group, or an organic amine salt. 9. The superabsorbent polymer of claim 7 , wherein the polymer is configured to be thermally degraded at a temperature of 180° C. or higher. 10. The superabsorbent polymer of claim 7 , further comprising a surface-crosslinked layer which is formed on the surface of the polymer. 11. The superabsorbent polymer of claim 7 , wherein the polymer has 5% to 30% increased centrifuge retention capacity (CRC) after exposure to a temperature of 185° C. for 40 minutes as compared with that before the exposure to the temperature of 185° C. for 40 minutes. 12. The superabsorbent polymer of claim 10 , wherein the surface-crosslinked layer is formed on the surface of the polymer by performing a surface crosslinking reaction at a temperature of 180° C. or higher. 13. The superabsorbent polymer of claim 10 , wherein the superabsorbent polymer has centrifuge retention capacity (CRC) from 33 g/g to 50 g/g and absorbency under pressure (AUP) of 0.7 psi of 21 g/g to 30 g/g.
having only {or additionally} carbon-to-carbon triple bonds as unsaturation in the carboxylic acid moiety · CPC title
Cross-linked polymers · CPC title
Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof · CPC title
Superabsorbents · 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.