Cellulosic and lignocellulosic structural materials and methods and systems for manufacturing such materials
US-9487915-B2 · Nov 8, 2016 · US
US2024209120A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2024209120-A1 |
| Application number | US-202318481918-A |
| Country | US |
| Kind code | A1 |
| Filing date | Oct 5, 2023 |
| Priority date | Dec 16, 2022 |
| Publication date | Jun 27, 2024 |
| Grant date | — |
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A method of preparing a lithium salt of carboxymethyl cellulose is provided. The method includes carrying out alkalization of cellulose in the presence of lithium hydroxide to generate an alkali product; and mixing the resulting product with a halogenated (e.g., halogen-including) acetic acid or a salt thereof to carry out etherification. An amine derivative is added to at least one of the alkalization or etherification.
Opening claim text (preview).
What is claimed is: 1 . A method of preparing a lithium salt of carboxymethyl cellulose, the method comprising: carrying out alkalization of cellulose and lithium hydroxide to form a resulting product; and mixing the resulting product with a halogenated acetic acid or a salt thereof to carry out etherification, wherein an amine derivative is added into the alkalization and/or the etherification. 2 . The method as claimed in claim 1 , wherein the amine derivative is represented by Chemical Formula 1 or Chemical Formula 2; wherein, in Chemical Formula 1, R 1 , R 2 , and R 3 are the same or different, and are each hydrogen, or an unsubstituted or halogen-substituted C1-C12 alkyl group; in Chemical Formula 2, R 4 , R 5 , R 7 , R 8 , and R 9 are the same or different, and are each hydrogen, or an unsubstituted or halogen-substituted C1-C12 alkyl group, R 6 is a C1-C12 alkenyl group, W 1 and We are the same or different and are each a C1 to C12 alkenyl group, and a is an integer of about 0 to about 2. 3 . The method as claimed in claim 1 , wherein the amine derivative is dimethylamine, diethylamine, trimethylamine, triethylamine, chloroalkyl amine, bromoalkyl amine, bis(chloro alkyl)amine, tris(chloro alkyl)amine, ethylene diamine, diethylene triamine, triethylene tetraamine, or one or more combinations thereof. 4 . The method as claimed in claim 1 , wherein the halogenated acetic acid is chloroacetic acid, fluoroacetic acid, bromoacetic acid, iodineacetic acid, or one or more combinations thereof. 5 . The method as claimed in claim 1 , wherein the salt of the halogenated acetic acid is a lithium salt of a halogenated acetic acid. 6 . The method as claimed in claim 1 , wherein an added amount of the amine derivative is 0.0001 parts by weight to 100 parts by weight based on 1 part by weight of the cellulose. 7 . The method as claimed in claim 1 , wherein the halogenated acetic acid or the salt thereof is added at an amount of about 0.1 parts by weight to about 100 parts by weight based on 1 part of the cellulose. 8 . The method as claimed in claim 1 , wherein the lithium salt of carboxymethyl cellulose has a degree of substitution of about 0.5 or more and about 1.5 or less. 9 . The method as claimed in claim 1 , wherein the alkalization is carried out in a solvent. 10 . The method as claimed in claim 9 , wherein the solvent is water, alcohol, or a combination thereof. 11 . A rechargeable lithium battery, comprising: a negative electrode comprising the lithium salt of carboxymethyl cellulose prepared by the method as claimed in claim 1 ; a positive electrode; and an electrolyte.
Negative electrodes · CPC title
Li-accumulators · CPC title
Selection of inactive substances as ingredients for active masses, e.g. binders, fillers · CPC title
Carboxycellulose, e.g. prepared by oxidation with nitrogen dioxide · CPC title
being polymers · CPC title
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