2018
DOI: 10.24193/subbchem.2018.4.02
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Fractal surface maghemite nanoparticles prepared by co-precipitation: the influence of Iron concentration and base nature

Abstract: Two series of magnetic nanopowders were synthesized at room temperature starting from a mixture of iron II and III precursors, FeSO4 and FeCl3, respectively. Precipitation agents, as KOH and NaOH were used. While the concentration of the added ferrous and ferric solutions ranged between 0.1 M and 0.0125 M, the hydroxide solution concentration was maintained constant (1 M). TEM images of the samples showed that the particles shape changes from quasi spherical to spherical. For both series the crystallite size d… Show more

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Cited by 5 publications
(3 citation statements)
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“…Average 10 nm diameter MNPs were obtained following a synthetic method previously reported [24]. To obtain an iron oxide-silica shell nanocomposite system with enhanced surface active area, the quantity of the TEOS used in the synthesis of MNPs 4 @SiO 2 was varied.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Average 10 nm diameter MNPs were obtained following a synthetic method previously reported [24]. To obtain an iron oxide-silica shell nanocomposite system with enhanced surface active area, the quantity of the TEOS used in the synthesis of MNPs 4 @SiO 2 was varied.…”
Section: Resultsmentioning
confidence: 99%
“…Separate batches of magnetic iron oxide nanoparticles were freshly obtained prior to each coating operation with various amounts of silica. MNPs were obtained by the alkaline reverse co-precipitation method using NaOH, following the synthetic strategy previously reported [24]. In particular, 43 mL FeCl 3 ·6H 2 O (0.1 M) and 25 mL FeSO 4 ·7H 2 O solutions (0.1 M) separately prepared were mixed and added to 25 mL NaOH solution (1 M).…”
Section: Synthesis Of Magnetic Mnps@sio2 Nanocompositesmentioning
confidence: 99%
“…The temperature requirement varies based on the precursor type [19]. To achieve a high degree of uniformity and a size ranging from 4 to 30 nm, the optimal temperature falls within the 100-350 • C range [31,32]. Some authors consider that the temperature, reaction time, type of surfactants and solvents, and aging period should be adjusted according to the desired shape and size [33,34].…”
Section: Thermal Decomposition Methodsmentioning
confidence: 99%