US2006254387A1PendingUtilityA1
Metal nano particle and method for manufacturing them and conductive ink
Est. expiryMay 10, 2025(expired)· nominal 20-yr term from priority
B22F 1/054B22F 9/24B82Y 30/00C09D 11/52H05K 1/097
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Claims
Abstract
A method of producing hydrophobic metal nanoparticles using a hydrophobic solvent, having uniform particle size distribution and high yield rate to allow mass production; the metal nanoparticles thus produced; and conductive ink including the metal nanoparticles are disclosed. According to one aspect of the invention, a method of producing metal nanoparticles is provided, comprising dissociating a metal compound with an amine-based compound, and adding a hydrocarbon-based compound and either one of an alkanoic acid or a thiol-based compound to the dissociated metal ion solution.
Claims
exact text as granted — not AI-modified1 . A method of producing metal nanoparticles, said method comprising:
dissociating a metal compound with an amine-based compound; and adding a hydrocarbon-based compound and either one of an alkanoic acid or a thiol-based compound to the dissociated metal ion solution.
2 . The method of claim 1 , wherein the metal compound includes one or more metals selected from a group consisting of silver (Ag), copper (Cu), nickel (Ni), gold (Au), platinum (Pt), palladium (Pd), and iron (Fe).
3 . The method of claim 2 , wherein the metal compound includes one or more compounds selected from a group consisting of AgNO 3 , AgBF 4 , AgPF 6 , Ag 2 O, CH 3 COOAg, AgCF 3 SO 3 , and AgClO 4 .
4 . The method of claim 1 , wherein the amine-based compound has a composition of C x H 2x+1 NH 2 , where x is an integer from 2 to 20.
5 . The method of claim 4 , wherein the amine-based compound is one or more compounds selected from a group consisting of butylamine, propylamine, octylamine, decylamine, dodecylamine, hexadecylamine, and oleylamine.
6 . The method of claim 1 , wherein the mole ratio of the amine-based compound to the metal compound ranges from 1 to 100.
7 . The method of claim 1 , wherein the hydrocarbon-based compound is one or more compounds selected from a group consisting of hexane, octane, decane, tetradecane, hexadecane, 1-hexadecene, 1-octadecene, toluene, xylene, and chlorobenzoic acid.
8 . The method of claim 1 , wherein the hydrocarbon-based compound is added so that the concentration of the metal compound becomes a mole ratio of 0.001 to 10.
9 . The method of claim 1 , wherein the alkanoic acid has a composition of RCOOH, where R is a saturated or unsaturated aliphatic hydrocarbon from C 1 to C 20 .
10 . The method of claim 9 , wherein the alkanoic acid is one or more acids selected from a group consisting of lauric acid, oleic acid, decanoic acid, and palmitic acid.
11 . The method of claim 1 , wherein the mole ratio of the alkanoic acid to the metal compound ranges from 0.1 to 1.
12 . The method of claim 1 , wherein the thiol-based compound has a composition of C y H 2y+1 SH, where y is an integer from 2 to 20.
13 . The method of claim 12 , wherein the thiol-based compound is one or compounds selected from a group consisting of linear-structure octanethiol, decanethiol, dodecanethiol, tetradecanethiol, hexadecanethiol, octadecanethiol and branched-structure 2-methyl-2-propanethiol.
14 . The method of claim 1 , wherein the mole ratio of the thiol-based compound to the metal compound ranges from 0.1 to 1.
15 . The method of claim 1 , wherein a reducing agent is further added during the adding of a hydrocarbon-based compound and either one of an alkanoic acid or a thiol-based compound to the dissociated metal ion solution.
16 . The method of claim 15 , wherein the reducing agent is one or more compounds selected from a group consisting of boron hydroxide, hydrazine, alcohol, amide, acid, and glucose.
17 . The method of claim 15 , wherein the reducing agent is one or more compounds selected from a group consisting of NaBH 4 , LiBH 4 , tetrabutylammonium borohydride, N 2 H 4 , glycol, glycerol, dimethylformamide, tannic acid, citrate, and glucose.
18 . The method of claim 15 , wherein the mole ratio of the reducing agent to the metal compound ranges from 0.1 to 1.
19 . Metal nanoparticles, produced by a method comprising:
dissociating a metal compound with an amine-based compound; and adding a hydrocarbon-based compound and an alkanoic acid to the dissociated metal ion solution.
20 . The metal nanoparticles of claim 19 , wherein the size of the metal nanoparticles is 1 to 40 nm.
21 . The metal nanoparticles of claim 19 , including 10 to 40 weight % organic components among the metal nanoparticles.
22 . The metal nanoparticles of claim 19 , used an antibiotic, a deodorant, a disinfectant, a conductive adhesive, a conductive ink, or an electromagnetic shield for a display device.
23 . Metal nanoparticles, produced by a method comprising:
dissociating a metal compound with an amine-based compound; and adding a hydrocarbon-based compound and a thiol-based compound to the dissociated metal ion solution.
24 . The metal nanoparticles of claim 23 , wherein the size of the metal nanoparticles is 1 to 20 nm.
25 . The metal nanoparticles of claim 23 , having 1 to 6 weight % of sulfur.
26 . The metal nanoparticles of claim 23 , used an antibiotic, a deodorant, a disinfectant, conductive adhesive, conductive ink, or an electromagnetic shield for a display device.
27 . Conductive ink including metal nanoparticles produced by a method comprising:
dissociating a metal compound with an amine-based compound; and adding a hydrocarbon-based compound and either one of an alkanoic acid or a thiol-based compound to the dissociated metal ion solution.Join the waitlist — get patent alerts
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