2019
DOI: 10.1002/cctc.201801539
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Hydrothermal Synthesis of a Novel Double‐Sided Nanobrush Co3O4 Catalyst and Its Catalytic Performance for Benzene Oxidation

Abstract: A double‐sided nanobrush Co3O4 (Co3O4−B) catalyst was successfully prepared by a hydrothermal method for the first time, and Co3O4 rods (Co3O4−R), Co3O4 hexagonal plates (Co3O4−H) and Co3O4 double‐sided helianthus discs (Co3O4−D) were also synthesized through tuning the water/ethanol ratio. Among all of the as‐prepared catalysts, the Co3O4−B catalyst exhibited the best catalytic activity for benzene oxidation. The excellent catalytic performance could be attributed to the surface abundance Co3+ species, good l… Show more

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Cited by 33 publications
(21 citation statements)
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“…Moreover, toluene conversion could be recovered to the initial conversion after the water vapor was cut off, because the H 2 O molecule was easily desorbed from the surface of catalysts at high temperature. Thus, the deactivation caused by water vapor is reversible …”
Section: Resultsmentioning
confidence: 57%
See 1 more Smart Citation
“…Moreover, toluene conversion could be recovered to the initial conversion after the water vapor was cut off, because the H 2 O molecule was easily desorbed from the surface of catalysts at high temperature. Thus, the deactivation caused by water vapor is reversible …”
Section: Resultsmentioning
confidence: 57%
“…Figure 3d shows the Thus, the deactivation caused by water vapor is reversible. 23 3.3. Chemical State and Electronic Properties.…”
Section: Methodsmentioning
confidence: 99%
“…Among them, catalytic oxidation has been considered one of the most promising technologies because it can completely convert VOCs under relatively low temperatures (<400 • C) into harmless CO 2 and H 2 O with low energy consumption, which has gained a lot of attention either in scientific and industrial fields. The key issue of catalytic oxidation is to design catalysts with high catalytic activity and low cost [6,7].…”
Section: Introductionmentioning
confidence: 99%
“…The region I is due to the desorption of chemically adsorbed O – species on the surface, which is surface-active oxygen and easily desorbs from the transition metal oxides’ surface. The region II is corresponding to the desorption of surface lattice oxygen O 2– that is quite difficult Figure b clearly shows that the peaks of O – species of Co 3 O 4 -HP are stronger and desorption peak areas are larger, indicating that huge amounts of surface reactive oxygen species of Co 3 O 4 -HP are more readily and fully released during the HCHO oxidation reaction .…”
Section: Resultsmentioning
confidence: 99%