2013
DOI: 10.1016/j.colsurfa.2013.01.025
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The competing effect of ammonia in the synthesis of iron oxide/silica nanoparticles in microemulsion/sol–gel system

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Cited by 28 publications
(11 citation statements)
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“…Iron oxide and compositei ron oxide/silicap owders were synthesized as described elsewhere [11].T able 1p resents the composition of the MEs used as synthetic systems. Non-encapsulatedi ron oxide samples with different surface areas (identified as F 1 and F 2 )a nd composite iron oxide/ silica (identified as FS) samples werep reparedb yd ropping 20.0 mL of ME 1b into ME 1a or ME 2b into ME 2a ,r espectively, under magnetic stirring.A ll mixtures were then sonicated (Marconi, 30 %a mplitudea nd cycleo f0 .2) for 30 min.…”
Section: Microemulsion (Me) Synthesismentioning
confidence: 99%
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“…Iron oxide and compositei ron oxide/silicap owders were synthesized as described elsewhere [11].T able 1p resents the composition of the MEs used as synthetic systems. Non-encapsulatedi ron oxide samples with different surface areas (identified as F 1 and F 2 )a nd composite iron oxide/ silica (identified as FS) samples werep reparedb yd ropping 20.0 mL of ME 1b into ME 1a or ME 2b into ME 2a ,r espectively, under magnetic stirring.A ll mixtures were then sonicated (Marconi, 30 %a mplitudea nd cycleo f0 .2) for 30 min.…”
Section: Microemulsion (Me) Synthesismentioning
confidence: 99%
“…For the samples as synthesized (F 1 ,F 2 and FS), bandsa round 1550 and 1400 cm À1 are due to organicr esiduesf rom the microemulsion synthesis, mainly the surfactant that strongly absorbs over the high surface area of the particles [11].T hese impurities are observed by all FT-IR techniques, indicating that the organicr esidues spread over the samples in at hick layer.H eatingi nduced the decomposition of this organic residue,l eaving no indication of impurities in the sample's FS 500 spectra. It is interesting to note that the transmission spectrum for the commercial F C sample shows only iron oxide bands, whilstD RIFT and UATR spectra also show bands around 1100 to 800 cm À1 ,w hich may indicate that the iron oxide particles are covered with av ery thin protective layer,n ot informed by the provider.…”
mentioning
confidence: 97%
“…It can be achieved by using different methods which consist of hydrolysis of alcoxysilane as tetraethoxysylane (TEOS) (Fernandes et al 2013;Teja and Koh 2009;Laurent and Mahmoudi 2011), in the presence of ammonia and superparamagnetic iron oxide nanoparticles. This precursor with the formula Si(OC 2 H 5 ) 4 contains four ethyl groups attached to SiO 4 , which is called orthosilicate (Fernandes et al 2013).…”
Section: Microemulsionmentioning
confidence: 99%
“…The preparation of magnetic iron oxide nanoparticles with controlled size and morphology has been carried out in water-in-oil microemulsion consisting of a cationic or non-ionic surfactant (Triton-X), a co-surfactant (glycols, hexanol, 1-butanol), oil phase (n-octane, cyclohexane) and aqueous phase (Fernandes et al 2013). The microemulsion is formed through addition of an aqueous solution with iron salt precursors to the surfactant/co-surfactant mixture.…”
Section: Microemulsionmentioning
confidence: 99%
“…This process yields cubic or spherical particles with characteristic narrow pore size ranging from 4 to 15 nm and high surface area (~315 m 2 g -1 ) [30,31] . Water-in-oil microemulsion consisting of a cationic or non-ionic surfactant (Triton-X), a co-surfactant (glycols, hexanol, 1-butanol), oil phase (n-octane, cyclohexane) and the aqueous phase is generally used to prepare magnetic iron oxide nanoparticles with controlled size and morphology [32] . The microemulsion is formed through the addition of an aqueous solution with iron salt precursors.…”
Section: Iron Oxide Nmmentioning
confidence: 99%