| CPC A61K 33/38 (2013.01) [A61K 9/14 (2013.01); A61P 35/00 (2018.01); C01B 25/45 (2013.01); C01G 3/02 (2013.01); C01P 2002/72 (2013.01); C01P 2002/82 (2013.01); C01P 2002/84 (2013.01); C01P 2002/85 (2013.01); C01P 2004/03 (2013.01); C01P 2004/32 (2013.01); C01P 2006/12 (2013.01); C01P 2006/14 (2013.01); C01P 2006/16 (2013.01)] | 10 Claims |
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1. A method of making Cu—Ag3PO4 nanoparticles, comprising:
first forming CuO by:
dissolving copper nitrate trihydrate in water in a polytetrafluoroethylene (PTFE) lined autoclave to form a dissolved copper nitrate trihydrate;
mixing trisodium citrate and ammonium fluoride into the dissolved copper nitrate trihydrate at a temperature less than 23° C. to form a solution;
heating the solution in the PTFE lined autoclave at a temperature over 120° C. for more than 10 hours;
centrifuging the heated solution and removing excess liquid from a CuO precipitate:
washing the CuO precipitate with ethanol and water;
drying the washed CuO precipitate at a temperature less than 150° C.; and
calcining the dried CuO precipitate at a temperature greater than 300° C. to form the CuO; then
forming a mixture of at least one silver salt, at least one phosphate salt, and the CuO;
dissolving the mixture in water;
sonicating the mixture; and
precipitating the Cu—Ag3PO4 nanoparticles;
wherein copper is present in the Cu—Ag3PO4 nanoparticles in an amount of 2 to 23 weight percent (wt. %) based on the total weight of the Cu—Ag3PO4 nanoparticles.
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