2004
DOI: 10.1016/j.apcata.2003.09.033
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Fe3−xMnxO4 catalysts: phase transformations and carbon monoxide oxidation

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Cited by 91 publications
(50 citation statements)
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“…Mn cations initially occupy the octahedral sites in the bulk structure, accelerate the electron transfer and improve the catalytic activity of magnetite, which is in accordance with previous studies in Refs. [13,23]. But with an increase in Mn content, partial Mn cations occupy the octahedral sites on magnetite surface.…”
Section: Resultsmentioning
confidence: 99%
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“…Mn cations initially occupy the octahedral sites in the bulk structure, accelerate the electron transfer and improve the catalytic activity of magnetite, which is in accordance with previous studies in Refs. [13,23]. But with an increase in Mn content, partial Mn cations occupy the octahedral sites on magnetite surface.…”
Section: Resultsmentioning
confidence: 99%
“…The octahedral Mn 2+ and Mn 3+ accelerate the electron transfer to regenerate the Fenton active species Fe 2+ , which leads to the strong Fenton activity of FM1 (Fig. A.1) [13,23]. Moreover, the catalytic performance of magnetites with lower Mn substitution than FM1 (Table A.1) was tested in the AOII degradation.…”
Section: Heterogeneous Fenton Activitymentioning
confidence: 99%
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“…5,6 Spinel ferrites are of great fundamental and technological importance due to their structural, electronic, magnetic, and catalytic properties. 7 An interesting feature of spinel ferrites is the possibility to replace iron cations by other metal cations while maintaining the spinel structure. 8 The physicochemical properties of spinel ferrites are strongly dependent on the site, nature, and amount of metal incorporated into the structure.…”
Section: Introductionmentioning
confidence: 99%
“…Ti 4+ [8], Cr 3+ [9], Mn 2+ [10], Co 2+ [11], and Ni 2+ [10]. Previous studies have investigated the effect of above substitutions on the heterogeneous Fenton catalytic activity of magnetite, which was greatly dependent on the occupancy, nature and amount of substituting metals [12][13][14]. For example, the catalytic activity relied on the octahedral cations rather than the tetrahedral ones, as the octahedral sites were almost exclusively exposed at the surface of inverse spinel structure [14].…”
Section: Introductionmentioning
confidence: 99%