Co-precipitation |
FeSO4·7H2O, FeCl3, NH4OH |
PVA |
Fe3O4, 4–10 nm |
[15] |
|
FeCl2, FeCl3, NH4OH, 25–80 °C, |
|
Fe3O4, 20 nm |
[16] |
|
FeSO4·7H2O, FeCl3·6H2O, NaOH |
Citrate or not |
Fe3O4, 8 nm with citrate, 14–28 nm without citrate |
[18] |
|
FeSO4·7H2O, FeCl3·6H2O, NH4OH, 80 °C |
Phosphate |
Fe3O4, 9–40 nm |
[20] |
|
Fe(acac)3, Co(acac)2, Oleic acid, benzyl ether, 290 °C |
|
CoxFe3–xO4, 35–110 nm |
[21] |
|
FeCl3, AlCl3·6H2O, CoCl2·6H2O, 70 °C |
|
CoFe2–xAlxO4, 20–63 nm |
[22] |
Thermodecomposition |
FeCl3·6H2O, 2-pyrrolidone, 245 °C, reflux 1–24 h |
|
Fe3O4, 4–60 nm |
[30] |
|
Fe(acac)3, 2-pyrrolidone, 200–240 °C |
α,ω-dicarboxyl-terminated poly(ethylene glycol) |
Fe3O4, 6–15 nm with average 11 nm |
[31] |
|
Fe(acac)3, oleylamine and benzyl ether, |
|
Fe3O4, 8 ± 0.4 nm |
[36] |
Combustion waves |
Fe2O3 NPs, nitrocellulose, 740 °C |
|
Fe3O4, 5–20 nm |
[37] |
Hydrothermal synthesis |
metal linoleate (solid), an ethanol–linoleic acid liquid phase, and a water–ethanol solution |
|
Fe3O4, 9 nm CoFe2O4, 12 nm |
[38] |
|
FeCl3, ethylene glycol, NaOAc, 200 °C |
|
Fe3O4–graphite, 100 nm |
[42] |
|
Composition controlled synthesis |
Various surfactants |
MFe2O4, M = Mg, Fe, Co, Ni, Cu, Zn, 3 nm |
[44] |
Emulsion synthesis |
Fe3O4, histidine |
|
Fe3O4–histidine composite, 500 nm |
[46] |
Microbial synthesis |
β-FeOOH, ZnxFe1–xOOH, Clostridium sp. |
|
Fe3O4, 5–10 nm using β-FeOOH, ZnxFe3–xO4, 3–8 nm using ZnxFe1–xOOH |
[47] |
|
β-FeOOH, S. putrefaciens CN32, 9,10-anthraquinone-2,6-disulfonate |
|
Fe3O4, framboidal, 20–50 nm |
[48] |
Green synthesis |
Natural biorenewable resources |
Plant extracts |
Fe3O4, hybrids |
[87] |