Metal organic framework-derived carbon aerogel, preparation method thereof and application in lithium ion batteries
US-12183924-B2 · Dec 31, 2024 · US
US9428387B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9428387-B2 |
| Application number | US-201214235642-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 26, 2012 |
| Priority date | Jul 27, 2011 |
| Publication date | Aug 30, 2016 |
| Grant date | Aug 30, 2016 |
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The present invention relates to a process for preparing a carbon foam, from selected oxocarbons or pseudo-oxocarbons, at low temperature and to the use of the material obtained via the implementation of this process for the manufacture of a system for detecting light waves.
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The invention claimed is: 1. A process for preparing a porous carbon material, wherein said method comprises at least one step of heat treatment at a temperature of at least 300° C., under a nonoxidizing atmosphere, of an organic molecule selected from the oxocarbons and oxocarbon derivatives of formulae (I-1) to (I-7) below: in which: R 1 to R 8 , R 13 to R 21 , and R 24 , independently of one another, represent OH; SH; an O-alkyl or S-alkyl group in which the alkyl radical is linear and has from 1 to 4 carbon atoms; an O-aryl or S-aryl group in which the aryl ring is a phenyl ring or a phenyl ring substituted in para position by an O-methyl or S-methyl group; or a group NR 25 R 26 in which the radicals R 25 and R 26 , which are identical or different, represent a C 1 -C 4 alkyl radical; R 9 to R 12 and R 22 and R 23 , independently of one another, represent an oxygen or sulfur atom; an N—CN (isocyano) group; or a C(CN) 2 (malononitrile) group. 2. The process as claimed in claim 1 , wherein in the compounds of formulae (I-1) to (I-7): the alkyl radical stated for R 1 to R 8 , R 13 to R 21 , and R 24 is a methyl radical; R 25 and R 26 are identical and represent a methyl. 3. The process as claimed in claim 1 , wherein the process employs an organic molecule selected from the compounds of formulae (I-1) to (I-7) in which the substituents R are selected from OH and O. 4. The process as claimed in claim 1 , wherein the organic molecule is a compound of formula (I-3) in which R 7 =R 8 =OH and R 9 =O, or a compound of formula (I-7) in which R 22 =R 23 =O and R 21 =R 24 =OH. 5. The process as claimed in claim 1 , wherein the heat treatment temperature is 400° C. 6. The process as claimed in claim 1 , wherein the nonoxidizing atmosphere is provided by a stream of dinitrogen, argon, helium, hydrogen, said streams being used alone or as a mixture. 7. The process as claimed in claim 1 , wherein the heat treatment is carried out at atmospheric pressure and without metal catalyst. 8. The process as claimed in claim 1 , wherein the organic starting molecule is used in powder form. 9. The process as claimed in claim 1 , wherein the duration of the heat treatment is from 2 to 4 hours. 10. The process as claimed in claim 1 , wherein the heat treatment is carried out with a temperature rise of from 1 to 10° C./minute, from the ambient temperature to the desired temperature.
Thermal treatment, e.g. calcining or pyrolizing · CPC title
Carbon-based electrodes · CPC title
Honeycomb or cellular structures; Solid foams or sponges · CPC title
being in the range 2-50 nm, i.e. mesopores · CPC title
comprising free carbon; comprising carbon obtained by carbonising processes · CPC title
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