Resin composition and manufacturing method thereof
US-2024400734-A1 · Dec 5, 2024 · US
US12590175B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12590175-B2 |
| Application number | US-202418649960-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 29, 2024 |
| Priority date | Jun 15, 2022 |
| Publication date | Mar 31, 2026 |
| Grant date | Mar 31, 2026 |
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The present disclosure relates to a hydrophilic polymer and a method for preparing the same. The hydrophilic polymer is characterized in that it is a copolymer of a conjugated diene, a monoolefin and a hydrophilic monomer represented by Formula I. In the Formula I, X 1 , X 2 and X 3 are each independently selected from hydrogen atoms, or a linear or branched alkyl with 1-4 carbon atoms. At least one of R 1 , R 2 and R 3 is hydrophilic group; and the others are each independently selected from hydrogen atoms or, an alkyl or alkoxy with 1-4 carbon atoms.
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What is claimed is: 1 . A hydrophilic polymer, wherein the hydrophilic polymer is a copolymer of a conjugated diene, a monoolefin and a hydrophilic monomer represented by Formula I, where X 1 and X 2 are hydrogen atoms, and X 3 is selected from alkyls with 1-4 carbon atoms; at least one of R 1 , R 2 and R 3 is hydrophilic group; and others are each independently selected from hydrogen atoms, or an alkyl or alkoxy with 1-4 carbon atoms. 2 . The hydrophilic polymer according to claim 1 , wherein the copolymer is a random copolymer; the conjugated diene is a conjugated diene with 4 or more carbon atoms, and selected from one or more of 1,3-butadiene, isoprene, 2,3-dimethyl-1,3-butadiene, 1,3-pentadiene, 2,4-hexadiene, 1, 3-cyclohexadiene, 2-chloro-1,3-butadiene, and/or the monoolefin is an aromatic monovinyl compound, and selected from one or more of styrene, α-methylstyrene, p-tert-butylstyrene, butoxystyrene, vinyltoluene, chlorostyrene, and vinylnaphthalene. 3 . The hydrophilic polymer according to claim 1 , wherein the hydrophilic group is selected from at least one of a hydroxyl, an amino, and a carboxyl. 4 . The hydrophilic polymer according to claim 1 , wherein at least two of R 1 , R 2 and R 3 are hydrophilic groups and others are each independently selected from hydrogen atoms, or alkyl with 1-4 carbon atoms. 5 . The hydrophilic polymer according to claim 1 , wherein a number average molecular weight Mn thereof is 12×10 4 -17×10 4 . 6 . The hydrophilic polymer according to claim 1 , wherein in the hydrophilic polymer, a ratio of parts by mass of the conjugated diene, the monoolefin, and the hydrophilic monomer is 10-90:90-10:1-6. 7 . A method for preparing a hydrophilic polymer, comprising a step of polymerizing a conjugated diene, a monoolefin, and a hydrophilic monomer represented by Formula I, where X 1 and X 2 are hydrogen atoms, and X 3 is selected from alkyls with 1-4 carbon atoms; at least one of the R 1 , R 2 and R 3 is hydrophilic group; and others are each independently selected from hydrogen atoms, or an alkyl or alkoxy with 1-4 carbon atoms. 8 . The method for preparing a hydrophilic polymer according to claim 7 , wherein a copolymer is a random copolymer; the conjugated diene is a conjugated diene with 4 or more carbon atoms, and selected from one or more of 1,3-butadiene, isoprene, 2,3-dimethyl-1,3-butadiene, 1,3-pentadiene, 2,4-hexadiene, 1, 3-cyclohexadiene, 2-chloro-1,3-butadiene and/or the monoolefin is an aromatic monovinyl compound, and selected from one or more of styrene, α-methylstyrene, p-tert-butylstyrene, butoxystyrene, vinyltoluene, chlorostyrene, and vinylnaphthalene. 9 . The method for preparing a hydrophilic polymer according to claim 7 , wherein the hydrophilic group is selected from at least one of a hydroxyl, an amino, and a carboxyl. 10 . The method for preparing a hydrophilic polymer according to claim 7 , wherein at least two of R 1 , R 2 and R 3 are hydrophilic groups, and others are each independently selected from hydrogen atoms, or an alkyl with 1-4 carbon atoms. 11 . The method for preparing a hydrophilic polymer according to claim 7 , wherein a number average molecular weight Mn thereof is 12×10 4 -17×10 4 . 12 . The method for preparing a hydrophilic polymer according to claim 7 , wherein in the hydrophilic polymer, a ratio of parts by mass of the conjugated diene, the monoolefin, and the hydrophilic monomer is 10-90:90-10:1-6. 13 . An electrode active material slurry, comprising an electrode active material, a dispersion medium, and the hydrophilic polymer according to claim 1 . 14 . A lithium ion secondary battery, wherein the lithium ion secondary battery comprises a positive pole plate, a negative pole plate, a separator and an electrolyte; wherein the negative pole plate comprises a negative pole membrane layer prepared from the electrode active material slurry according to claim 13 . 15 . A battery pack, wherein the battery pack comprises the lithium ion secondary battery according to claim 14 . 16 . An electrical device, wherein the electrical device comprises the lithium ion secondary battery according to claim 14 .
Negative electrodes · CPC title
Electrodes composed of, or comprising, active material · CPC title
Energy storage using batteries · CPC title
with conjugated dienes · CPC title
Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title
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