Multiphase nanocomposite material production
A rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material includes a rhombohedral zinc orthosilicate (Zn 2 SiO 4 ) phase, a cubic zinc ferrite (ZnFe 2 O 4 ) phase, and a hexagonal silicon dioxide (SiO 2 ) phase. The rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material exhibits a morphology including spherical microscale particles with an average diameter ranging from 0.8 micrometer (μm) to 1.8 μm and irregular nanoscale aggregates with an average diameter ranging from 50 nanometer (nm) to 110 nm. The rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material has an adsorption capacity for basic fuchsin dye of greater than or equal to 140 milligrams per gram (mg/g). Furthermore, a method for producing the rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material includes calcination of metal precursors.
1 . A rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material, comprising:
a rhombohedral Zn 2 SiO 4 phase;
a cubic ZnFe 2 O 4 phase; and
a hexagonal SiO 2 phase,
wherein the rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 Oz/hexagonal SiO 2 /C nanocomposite material has a morphology comprising spherical microscale particles with an average diameter in a range from 0.8 to 1.8 μm and irregular nanoscale aggregates with an average diameter in a range from 50 to 110 nm, and
wherein rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material has an adsorption capacity for basic fuchsin dye of greater than or equal to 140 mg/g,
wherein the oxygen content is in a range from 40 to 60 atomic % (at. %), the silicon content is in a range from 20 to 30 at. %, the zinc content is in a range from 8 to 18 at. %, the iron content is in a range from 5 to 10 at. %, and the carbon content is in a range from 0.5 to 10 at. %.
2 . The rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material of claim 1 , wherein the spherical microscale particles with an average diameter in a range from 1 to 1.5 μm.
3 . The rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material of claim 2 , wherein the spherical microscale particles with an average diameter in a range from 1.1 to 1.3 μm.
4 . The rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 Oz/hexagonal SiO 2 /C nanocomposite material of claim 1 , wherein the irregular nanoscale aggregates with an average diameter in a range from 60 to 100 nm.
5 . The rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material of claim 4 , wherein the irregular nanoscale aggregates with an average diameter in a range from 70 to 90 nm.
6 . The rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material of claim 1 , wherein the rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material has an average crystallite size in a range from 50 to 70 nm.
7 . The rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material of claim 6 , wherein the rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material has an average crystallite size in a range from 55 to 65 nm.
8 . The rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material of claim 1 , wherein rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material has an adsorption capacity for basic fuchsin dye of greater than or equal to 150 mg/g.
9 . The rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material of claim 8 , wherein rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material has an adsorption capacity for basic fuchsin dye of greater than or equal to 155 mg/g.
10 . A rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material, comprising:
a rhombohedral Zn 2 SiO 4 phase;
a cubic ZnFe 2 O 4 phase; and
a hexagonal SiO 2 phase,
wherein the rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material has a morphology comprising spherical microscale particles with an average diameter in a range from 0.8 to 1.8 μm and irregular nanoscale aggregates with an average diameter in a range from 50 to 110 nm, and
wherein rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material has an adsorption capacity for basic fuchsin dye of greater than or equal to 140 mg/g,
wherein the oxygen content is in a range from 45 to 55 atomic % (at. %), the silicon content is in a range from 22 to 27 at. %, the zinc content is in a range from 10 to 15 at. %, the iron content is in a range from 6 to 9 at. %, and the carbon content is in a range from 2 to 8 at. %.
11 . A method of producing the rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material of claim 1 , comprising:
adding NH 4 OH to a solution comprising Zn(NO 3 ) 2 ·6H 2 O, Fe(NO 3 ) 3 ·9H 2 O, and vinyltrimethoxysilane, forming a reaction mixture;
stirring the reaction mixture for 1 h, forming a gel precipitate;
filtering and washing the gel precipitate with distilled water to form a washed precipitate;
drying the washed precipitate at 100° C. to form a dried precipitate; and
calcining the dried precipitate at a temperature in a range from 600° C. to 800° C. for 1 to 5 hours to form the rhombohedral Zn 2 SiO 4 /cubic ZnFe 2 O 4 /hexagonal SiO 2 /C nanocomposite material.
12 . The method of claim 11 , wherein the concentration of NH 4 OH in the reaction mixture is in a range from 50 to 70 ml/L.
13 . The method of claim 11 , wherein the concentration of Zn(NO 3 ) 2 ·6H 2 O in the reaction mixture is in a range from 80 to 100 g/L.
14 . The method of claim 11 , wherein the concentration of Fe(NO 3 ) 3 ·9H 2 O in the reaction mixture is in a range from 110 to 140 g/L.
15 . The method of claim 11 , wherein the concentration of vinyltrimethoxysilane in the reaction mixture is in a range from 300 to 500 ml/L.
16 . The method of claim 11 , wherein the dried precipitate is calcined at 650° C. to 750° C.
17 . The method of claim 16 , wherein the dried precipitate is calcined at 700° C.
18 . The method of claim 11 , wherein the dried precipitate is calcined for 2 to 4 hours.
19 . The method of claim 11 , wherein the dried precipitate is calcined for 3 hours.