2020
DOI: 10.3390/molecules25030740
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Ultrasound and Radiation-Induced Catalytic Oxidation of 1-Phenylethanol to Acetophenone with Iron-Containing Particulate Catalysts

Abstract: Iron-containing particulate catalysts of 0.1–1 µm size were prepared by wet and ball-milling procedures from common salts and characterized by FTIR, TGA, UV-Vis, PXRD, FEG-SEM, and XPS analyses. It was found that when the wet method was used, semi-spherical magnetic nanoparticles were formed, whereas the mechanochemical method resulted in the formation of nonmagnetic microscale needles and rectangles. Catalytic activity of the prepared materials in the oxidation of 1-phenylethanol to acetophenone was assessed … Show more

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Cited by 6 publications
(10 citation statements)
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References 31 publications
(59 reference statements)
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“…The reduction of 4-NP (E 0 = −0.76 V) by NaBH 4 (E 0 = −1.33 V) is thermodynamically feasible, but kinetically restricted in the absence of a catalyst [41,42] in aqueous NaBH 4 . Our results confirm that the reaction does not proceed in a pure aqueous NaBH 4 solution.…”
Section: Reduction Of 4-nitrophenol Using Re/c and Re/g Catalystsmentioning
confidence: 99%
See 1 more Smart Citation
“…The reduction of 4-NP (E 0 = −0.76 V) by NaBH 4 (E 0 = −1.33 V) is thermodynamically feasible, but kinetically restricted in the absence of a catalyst [41,42] in aqueous NaBH 4 . Our results confirm that the reaction does not proceed in a pure aqueous NaBH 4 solution.…”
Section: Reduction Of 4-nitrophenol Using Re/c and Re/g Catalystsmentioning
confidence: 99%
“…In the present catalytic system, contrary to what was observed by other authors [41], no induction time was noticed. Such a reported induction period was linked [41] to the level of dissolved oxygen in the reaction medium, [42][43][44][45][46] and it ended once the level fell below a critical value that was dependent upon the metal nanoparticles used as the catalyst.…”
Section: Reduction Of 4-nitrophenol Using Re/c and Re/g Catalystsmentioning
confidence: 99%
“… [93] Compared with the 70% desulfurization rate in a 6 h oxidative process, the ultrasound-assisted oxidation could reach a 90% desulfurization rate in 3.5 h. In the Han’s study, [94] the photocatalytic CdO took place of the polyoxometalate to apply in the ultrasound-assisted oxidative technology of organic sulfur removal from the diesel as well, and under the optimal condition, this oxidative approach was efficient for sulfur removal and reached a 99.47% desulfurization degree. Alternatively, iron materials have been also used in the ultrasound-induced catalytic oxidation, for example, the oxidation of 1-phenylethanol to acetophenone was carried out in the Ribeiro’s study, [95] and the activation of iron-containing particulate catalysts under the ultrasound could significantly increase the overall effectiveness of catalytic system.…”
Section: Oxidationmentioning
confidence: 99%
“…4,5 Hence, activating C-H bonds in materials and converting these useless materials into valuable compounds is an important, economic and green step in synthetic chemistry. 6,7 Up to now, a few catalysts such as noble metals (Pd, Ru), 1,8 non-noble metal catalysts, 9,10 earth abundant metal catalysts, 11,12 and organic molecules 13,14 have been selected for the conversion of alkylbenzenes; however, some of these are neither recyclable nor inexpensive. Therefore, an economical and efficient heterogeneous catalyst without any additives is more desirable.…”
Section: Introductionmentioning
confidence: 99%