Jun Wang’s research while affiliated with University of Shanghai for Science and Technology and other places

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Fig. 3 Light-off curves of the catalytic combustion of methane over the NiO/CeO 2 catalysts (gas space velocity = 60000 mL$g -1 $h -1 ).
Fig. 4 Effect of the addition of water vapor in CH 4 combustion over 10 wt-% NiO/CeO 2 : (a) without H 2 O and (b) with 3.1% water vapor (25°C; gas space velocity = 60000 mL$g -1 $h -1 ).
Fig. 5 Dependence of the reaction rates on the CH 4 and O 2 concentration over the 10 wt-% NiO/CeO 2 catalyst at 320°C: (a) 0.5-4 vol-% CH 4 , 4 vol-% O 2 , in Ar; (b) 2-10 vol-% O 2 , 1 vol-% CH 4 , in Ar. (P CH 4 and P O 2 , partial pressures; gas space velocity = 30000 mL$g -1 $h -1 ).
Fig. 6 Arrhenius plots of the reaction rate of CH 4 combustion (activation energy, E a ) over (a) pure CeO 2 and (b) 10 wt-% NiO/ CeO 2 (gas space velocity = 30000 mL$g -1 $h -1 ).
Fig. 7 XRD patterns of the NiO/CeO 2 samples with various NiO loadings.

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Catalytic combustion of methane over a highly active and stable NiO/CeO2 catalyst
  • Article
  • Full-text available

September 2019

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326 Reads

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26 Citations

Frontiers of Chemical Science and Engineering

Xiuhui Huang

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Junfeng Li

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Jun Wang

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In the last decades, many reports dealing with technology for the catalytic combustion of methane (CH4) have been published. Recently, attention has increasingly focused on the synthesis and catalytic activity of nickel oxides. In this paper, a NiO/CeO2 catalyst with high catalytic performance in methane combustion was synthesized via a facile impregnation method, and its catalytic activity, stability, and water-resistance during CH4 combustion were investigated. X-ray diffraction, low-temperature N2 adsorption, thermogravimetric analysis, Fourier transform infrared spectroscopy, hydrogen temperature programmed reduction, methane temperature programmed surface reaction, Raman spectroscopy, electron paramagnetic resonance, and transmission electron microscope characterization of the catalyst were conducted to determine the origin of its high catalytic activity and stability in detail. The incorporation of NiO was found to enhance the concentration of oxygen vacancies, as well as the activity and amount of surface oxygen. As a result, the mobility of bulk oxygen in CeO2 was increased. The presence of CeO2 prevented the aggregation of NiO, enhanced reduction by NiO, and provided more oxygen species for the combustion of CH4. The results of a kinetics study indicated that the reaction order was about 1.07 for CH4 and about 0.10 for O2 over the NiO/CeO2 catalyst.

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Citations (1)


... Moreover, the S 2p spectrum of NiOOH@Ni3S2/NF also revealed two new peaks at 165.0 and 163.8 eV in addition to the ones of 2p3/2 and 2p1/2 of S 2-( Figure S2 in the ESM), demonstrating the formation of oxysulfide (S-Ni-O) bonds due to the partial oxidation of Ni3S2 to NiOOH [52][53][54][55][56]. The existence of both NiOOH and Ni3S2 species was also confirmed by Raman characterization (Figure 1c), where the peaks at 202,225,249,305,328 and 353 cm -1 corresponded to the vibration modes of rhombohedral Ni3S2 [57][58][59], and the ones at 455 and 619 cm -1 were attributed to the bending vibration (Eg) and symmetric stretching vibration (A1g) of Ni-O in NiOOH [60][61][62][63]. ...

Reference:

Electrochemical co-upgrading CO 2 and glycerol for selective formate production with 190% overall Faradaic efficiency
Catalytic combustion of methane over a highly active and stable NiO/CeO2 catalyst

Frontiers of Chemical Science and Engineering