2011
DOI: 10.1016/j.jhazmat.2010.09.068
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Magnetic Fe2MO4 (M:Fe, Mn) activated carbons: Fabrication, characterization and heterogeneous Fenton oxidation of methyl orange

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Cited by 305 publications
(98 citation statements)
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“…The magnetization reaches zero when the magnetic field is removed because the iron oxide particles are of single-crystal domain with one orientation of the magnetic moment. The saturation magnetization values, found to be rs = 0.1 emu g −1 and rs = 0.35 emu g −1 for NF and NFM impregnated carbons, respectively, are less than those for Fe 3 O 4 nanoparticles (Ms = 58.94 emu g −1 ) [38], and bare Fe 2 MnO 4 nanoparticles (Ms = 70 emu g −1 ) [39]. This decrease can be attributed to the existence of graphitic layers on the surface of magnetic nanoparticles [35].…”
Section: Materials Characterizationmentioning
confidence: 79%
See 1 more Smart Citation
“…The magnetization reaches zero when the magnetic field is removed because the iron oxide particles are of single-crystal domain with one orientation of the magnetic moment. The saturation magnetization values, found to be rs = 0.1 emu g −1 and rs = 0.35 emu g −1 for NF and NFM impregnated carbons, respectively, are less than those for Fe 3 O 4 nanoparticles (Ms = 58.94 emu g −1 ) [38], and bare Fe 2 MnO 4 nanoparticles (Ms = 70 emu g −1 ) [39]. This decrease can be attributed to the existence of graphitic layers on the surface of magnetic nanoparticles [35].…”
Section: Materials Characterizationmentioning
confidence: 79%
“…The position and relative intensity of diffraction peaks presented in Figure 4 can be indexed to the standard data for Fe 2 MO 4 bulk magnetite (JCPDS file No. 10-0319) [38]. There was not detected peak for manganese oxide implying incorporation of manganese ions into the crystal structure of Fe 3 O 4 [39] leading to the formation of Fe 2 MO 4 (M:Fe and/or Mn).…”
Section: Materials Characterizationmentioning
confidence: 95%
“…Throughout the reaction, Solutions of dye were prepared by using ultrapure water (MILLIPORE, direct-Q, UV3 With Pump) and the reactant solution was adjusted to constant pH with dilute aqueous HCl 0.01M or NaOH 0.01M solutions. the taking away were carried out by filtered using a syringe filter of diameter 0,45μm (Minisart, sartorium stedim biotech).The degradation progress was monitored by spectrometric measurements using a spectrophotometer (Jasco V530) with its adsorption at 465nm for samples that had pH> 3 and at 500nm for samples that had pH≤3 [15].The effects of various experimental parameters such as the temperature, catalyst dosage, and H 2 O 2 amount were investigated. The average degradation in terms of the percentage of MO in solution was calculated using the following formula:…”
Section: Ii-5 Experimental Procedures and Analytical Methodsmentioning
confidence: 99%
“…Treatment with HNO 3 (Ultrex Baker) for GAC was important [22], as it was intended to insert oxygen to structural surface of the coals, following the ideas of Nguyen [23] and Shi [24], who studied that oxygen complexes can be formed on surface of activated carbon by modifying its surface chemistry. GAC's were contacted with concentrated HNO 3 in a proportion of 100 g of carbon and 300 ml of acid; it was stirred for 8 h as in HCl case.…”
Section: The Gac Pre-treatment With Hno3mentioning
confidence: 99%