Electroconductive polyamide resin composition
US-9206048-B2 · Dec 8, 2015 · US
US9416009B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9416009-B2 |
| Application number | US-201013380450-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 28, 2010 |
| Priority date | Jun 26, 2009 |
| Publication date | Aug 16, 2016 |
| Grant date | Aug 16, 2016 |
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The invention relates to a method of modifying electrical properties of carbon nanotubes by subjecting a composition of carbon nanotubes to one or more radical initiator(s). The invention also relates to an electronic component such as field-effect transistor comprising a carbon nanotube obtained using the method of the invention. The invention also relates to the use of the modified carbon nanotubes in conductive and high-strength nanotube/polymer composites, transparent electrodes, sensors and nanoelectromechanical devices, additives for batteries, radiation sources, semiconductor devices (e.g. transistors) or interconnects.
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The invention claimed is: 1. A method for enriching specific species of carbon nanotubes according to their electronic properties and/or their diameter, comprising modifying the electrical properties of carbon nanotubes by subjecting a composition of carbon nanotubes to one or more radical initiator(s), wherein the modification is carried out in the presence of one or more alkene(s) or one or more alkyne(s) or mixtures thereof to produce C—C radicals, wherein the alkene or alkyne is substituted with one or more electron-withdrawing groups, and wherein the specific species of carbon nanotubes to be enriched comprises single-walled semiconducting carbon nanotubes; wherein the method comprises: mixing the composition of carbon nanotubes with the one or more radical initiator(s) in an organic solvent or a mixture of organic solvents to form a mixture, wherein the radical initiator is selected from the group consisting of organic peroxides, inorganic initiators, halogen-containing compounds and mixtures thereof; activating the one or more radical initiator(s) to form radicals; reacting the carbon nanotubes with the radicals, wherein the radicals preferably react with those species of carbon nanotubes different from the specific species of carbon nanotubes to be enriched; and separating the modified carbon nanotubes from the unmodified carbon nanotubes, thereby enriching the specific species of carbon nanotubes. 2. The method as claimed in claim 1 , wherein the carbon nanotubes are a mixture of nanotubes with different electronic properties and/or sizes. 3. The method of claim 1 , wherein the modified carbon nanotubes comprise metallic carbon nanotubes. 4. The method of claim 1 , wherein modification of electronic properties allowing the enrichment of the specific species of carbon nanotubes further allows suppressing the electronic properties of metallic single-walled carbon nanotubes. 5. The method of claim 1 , wherein the organic peroxides are selected from the group consisting of methyl ethyl ketone peroxide, benzoyl peroxide, acetone peroxide, pinane hydroperoxide, cumene hydroperoxide, tert-butyl hydroperoxide (TBHP), 1,1-bis(tert-amylperoxy)cyclohexane, 1,1-bis(tert-butylperoxy)-3,3,5-trimethylcyclohexane, 1,1-bis(tert-butylperoxy)cyclohexane, 2,2-bis(tert-butylperoxy)butane, 2,4-pentanedione peroxide, 2,5-bis(tert-butylperoxy)-2,5-dimethylhexane, 2,5-di(tert-butylperoxy)-2,5-dimethyl-3-hexyne, 2-butanone peroxide, di-tert-amyl peroxide, tert-butylperoxy octoate, tert-butylperoxy neodecanoate, tert-butylperoxy isobutarate, dicumyl peroxide, lauroyl peroxide, tert-amylperoxy pivalate, tert-butylperoxy pivalate, tert-butyl peroxyacetate, tert-butyl peroxybenzoate, tert-butylperoxy 2-ethylhexyl carbonate and mixtures thereof. 6. The method of claim 1 , wherein the inorganic initiators are selected from the group consisting of hydrogen peroxide, ammonium persulfate, hydroxymethanesulfinic acid monosodium salt dihydrate, potassium persulfate, sodium persulfate and mixtures thereof. 7. The method of claim 1 , wherein the halogen-containing molecules are selected from the group consisting of fluorine- and chlorine-containing molecules. 8. The method of claim 1 , wherein mixing the composition of carbon nanotubes is carried out by sonicating or stirring or shaking the mixture. 9. The method of claim 1 , wherein the radical initiators are activated by thermal heating, light irradiation, redox initiation and/or sonication. 10. The method of claim 1 , wherein the organic solvent is selected from the group consisting of hexane, heptane, cyclohexane, benzene, toluene, pyridine, dichloromethane, chloroform, carbon tetrachloride, carbon disulfide, tetrahydrofuran, dioxane, diethyl ether, diisopropylether, ethylene glycol monobutyl ether, methyl ethyl ketone, methyl isobutyl ketone, acetone, cyclohexanone, ethyl acetate, isobutyl isobutyrate, ethylene glycol diacetate, dimethylformamide, acetonitrile, N,N-dimethyl acetamide, nitromethane, acetonitrile, N-methylpyrrolidone, dimethylsulfoxide water, methanol, ethanol, butyl alcohol and formic acid. 11. The method of claim 1 , wherein the separation is carried out by filtration, centrifugation and/or settling. 12. The method of claim 1 , wherein the reaction is carried at room temperature. 13. The method of claim 1 , wherein the separated carbon nanotubes are washed with an organic solvent.
Nanotechnology for information processing, storage or transmission, e.g. quantum computing or single electron logic · CPC title
Electricity · mapped topic
Nanotechnology for materials or surface science, e.g. nanocomposites · CPC title
Chemistry & Metallurgy · mapped topic
Carbon or graphite · CPC title
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