Polymer, composite positive active material including the same, and lithium secondary battery including electrode including the positive active material
US-2020148797-A1 · May 14, 2020 · US
US2022017670A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2022017670-A1 |
| Application number | US-202117371421-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 9, 2021 |
| Priority date | Jul 13, 2020 |
| Publication date | Jan 20, 2022 |
| Grant date | — |
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The present disclosure relates to a composition that includeswhere R includes a reactive end group, R1 includes a first bridging group, 1≤x≤100, and 1≤y≤100.
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What is claimed is: 1 . A composition comprising: wherein: R comprises a reactive end group, R 1 comprises a first bridging group, 1≤x≤100, and 1≤y≤100. 2 . The composition of claim 1 , wherein: R comprises at least one of 3 . The composition of claim 2 , wherein: R 1 comprises at least one of R 2 comprises a second bridging group, and 1≤u≤100. 4 . The composition of claim 3 , wherein: R 2 comprises at least one of 5 . The composition of claim 3 , wherein: R 1 is 6 . The composition of claim 5 , further comprising: wherein: 1≤m≤100, and 1≤n≤100. 7 . The composition of claim 6 , comprising at least one of, 8 . The composition of claim 1 , comprising a tensile strength between about 20 MPa and about 100 MPa. 9 . The composition of claim 1 , comprising a modulus between about 0.5 GPa and about 3.0 GPa. 10 . The composition of claim 1 , comprising an elongation at break between about 0.1% and about 100%. 11 . The composition of claim 1 , comprising a glass transition temperature between about 0° C. and about 250° C. 12 . A method comprising: reacting a first functionalized intermediate with a second functionalized intermediate to form a product, wherein: the first functionalized intermediate comprises the second functionalized intermediate comprises the product comprises, R comprises a reactive end group, R 1 comprises a first bridging group, 1≤x≤100, and 1≤y≤100. 13 . The method of claim 12 , further comprising: prior to the reacting, in a first mixture comprising a deconstruction product and a functionalized reactant, functionalizing the deconstruction product, wherein: the deconstruction product comprises the functionalized intermediate comprises at least one of and the functionalizing produces the first functionalized intermediate comprising and the second functionalized intermediate comprising 14 . The method of claim 12 , wherein: the reacting is performed using a second mixture of the first functionalized intermediate and the second functionalized intermediate, and the first functionalized intermediate and the second functionalized intermediate are at a molar ratio between about 1:2 and about 1:1. 15 . The method of claim 14 , wherein the second mixture has a viscosity between about 800 cP and 1200 cP at when measured at a temperature of about 25° C. 16 . The method of claim 12 , wherein the reacting is performed at a temperature between 20° C. and 150° C. 17 . The method of claim 12 , wherein the reacting is photoinitiated at a wavelength between 254 nm and 500 nm. 18 . The method of claim 12 , wherein the reacting is photoinitiated using at least one of diphenyl(2,4,6-trimethylbenzoyl)phosphine oxide (TPO), ethyl (2,4,6-trimethylbenzoyl) phenylphosphinate (TPO-L), or phenylbis(2,4,6-trimethylbenzoyl)phosphine oxide (BAPO). 19 . The method of claim 13 , further comprising: prior to the functionalizing, deconstructing a plastic, wherein: the deconstructing results in the forming of the deconstruction product. 20 . The method of claim 19 , wherein the plastic comprises at least one of polyethylene terephthalate, glycol modified polyethylene terephthalate, polybutylene terephthalate, polytrimethylene terephthalate, polyethylene naphthalate, or polyethylene 2,5-furandicarboxylate.
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