Method for preparing nanometer molybdenum disulfide powder
A nano-molybdenum disulfide and powder technology, applied in the direction of molybdenum sulfide, etc., can solve the problems that it is difficult to obtain a product with uniform composition, cannot obtain a two-dimensional lamellar structure, and the grain size distribution is uneven, and the grain size can be reached. Uniform and controllable, low cost, and the effect of improving purity
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[0034] Example 1:
[0035] Add 10mmol of ammonium molybdate and 20mmol of thiourea to the beaker, add 100ml of deionized water to the beaker, stir for 1 hour to fully dissolve the ammonium molybdate and thiourea, and transfer the solution into a 150ml volume of polyamide after the dissolution is complete. The tetrafluoroethylene-lined reaction kettle was sealed; the reaction kettle was placed in an electric heating oven, the oven temperature was set to 220°C, and the reaction time was set to 24 hours; when the reaction time expired, the reaction kettle was taken out, and the inner The mixture in the lining was suction filtered and dried; the dried solid was placed in a beaker, an aqueous solution with a volume fraction of 30% isopropanol was added, and after ultrasonic peeling for 5 hours, the dispersion was transferred to a centrifuge tube, and the centrifugation speed was 5000r / min. Under centrifugation, the supernatant liquid is retained and the solids therein are collected...
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[0036] Example 2:
[0037] Add 10mmol of ammonium molybdate and 20mmol of thiourea to the beaker, add 100ml of deionized water to the beaker, stir for 1 hour to fully dissolve the ammonium molybdate and thiourea, and transfer the solution into a 150ml volume of polyamide after the dissolution is complete. The tetrafluoroethylene-lined reaction kettle was sealed; the reaction kettle was placed in an electric heating oven, the oven temperature was set to 220°C, and the reaction time was set to 18 hours; when the reaction time was up, the reaction kettle was taken out, and the inner The mixture in the lining was suction filtered and dried; the dried solid was placed in a beaker, an aqueous solution with a volume fraction of 50% isopropanol was added, and after ultrasonic peeling for 5 hours, the dispersion was transferred to a centrifuge tube, and the centrifugation speed was 7000r / min. Centrifuge, retain the supernatant and collect the solids therein, and the obtained product is...
Example Embodiment
[0038] Example 3:
[0039] Add 10mmol of ammonium molybdate and 20mmol of thiourea to the beaker, add 100ml of deionized water to the beaker, stir for 1 hour to fully dissolve the ammonium molybdate and thiourea, and transfer the solution into a 150ml volume of polyamide after the dissolution is complete. The tetrafluoroethylene-lined reaction kettle was sealed; the reaction kettle was placed in an electric heating oven, the oven temperature was set to 240°C, and the reaction time was set to 9 hours; when the reaction time expired, the reaction kettle was taken out, and the inner The mixture in the lining was suction filtered and dried; the dried solid was placed in a beaker, an aqueous solution with a volume fraction of 60% isopropanol was added, and after ultrasonic peeling for 8 hours, the dispersion was transferred to a centrifuge tube, and the centrifugation speed was 12000 r / min. Centrifuge, retain the supernatant and collect the solids therein, and the obtained product ...
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