scholarly journals Probing the thermal-enhanced catalytic activity of CO oxidation over Pd/OMS-2 catalysts

RSC Advances ◽  
2017 ◽  
Vol 7 (66) ◽  
pp. 41936-41944 ◽  
Author(s):  
Xin Liu ◽  
Qiulin Zhang ◽  
Ping Ning ◽  
Qixian Liu ◽  
Zhongxian Song ◽  
...  

An elevating calcination temperature within 500 °C lead to the spill-over of the palladium, the increase of surface palladium abundance and catalytic activity. Phase transformation of OMS-2 and deactivation of the catalyst happened above 500 °C.

2016 ◽  
Vol 32 (3) ◽  
pp. 455-460 ◽  
Author(s):  
Xiaodong Zhang ◽  
Han Dong ◽  
Di Zhao ◽  
Yin Wang ◽  
Yangang Wang ◽  
...  

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 131 ◽  
Author(s):  
Rola Mohammad Al Soubaihi ◽  
Khaled Mohammad Saoud ◽  
Myo Tay Zar Myint ◽  
Mats A. Göthelid ◽  
Joydeep Dutta

Carbon monoxide (CO) oxidation is considered an important reaction in heterogeneous industrial catalysis and has been extensively studied. Pd supported on SiO2 aerogel catalysts exhibit good catalytic activity toward this reaction owing to their CO bond activation capability and thermal stability. Pd/SiO2 catalysts were investigated using carbon monoxide (CO) oxidation as a model reaction. The catalyst becomes active, and the conversion increases after the temperature reaches the ignition temperature (Tig). A normal hysteresis in carbon monoxide (CO) oxidation has been observed, where the catalysts continue to exhibit high catalytic activity (CO conversion remains at 100%) during the extinction even at temperatures lower than Tig. The catalyst was characterized using BET, TEM, XPS, TGA-DSC, and FTIR. In this work, the influence of pretreatment conditions and stability of the active sites on the catalytic activity and hysteresis is presented. The CO oxidation on the Pd/SiO2 catalyst has been attributed to the dissociative adsorption of molecular oxygen and the activation of the C-O bond, followed by diffusion of adsorbates at Tig to form CO2. Whereas, the hysteresis has been explained by the enhanced stability of the active site caused by thermal effects, pretreatment conditions, Pd-SiO2 support interaction, and PdO formation and decomposition.


Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 312 ◽  
Author(s):  
Antonella Glisenti ◽  
Andrea Vittadini

The effects of modifying the composition of LaCoO3 on the catalytic activity are predicted by density functional calculations. Partially replacing La by Sr ions has benefical effects, causing a lowering of the formation energy of O vacancies. In contrast to that, doping at the Co site is less effective, as only 3d impurities heavier than Co are able to stabilize vacancies at high concentrations. The comparison of the energy profiles for CO oxidation of undoped and of Ni-, Cu-m and Zn-doped (La,Sr)CoO3(100) surface shows that Cu is most effective. However, the effects are less spectacular than in the SrTiO3 case, due to the different energetics for the formation of oxygen vacancies in the two hosts.


2011 ◽  
Vol 133 (10) ◽  
pp. 3444-3451 ◽  
Author(s):  
Fan Yang ◽  
Jesús Graciani ◽  
Jaime Evans ◽  
Ping Liu ◽  
Jan Hrbek ◽  
...  

2004 ◽  
Vol 97 (3/4) ◽  
pp. 203-208 ◽  
Author(s):  
Yasuo Iizuka ◽  
Aya Kawamoto ◽  
Kazuhiro Akita ◽  
Masakazu Daté ◽  
Susumu Tsubota ◽  
...  

2019 ◽  
Vol 777 ◽  
pp. 655-662 ◽  
Author(s):  
A.V. Egorysheva ◽  
O.G. Ellert ◽  
E. Yu Liberman ◽  
D.I. Kirdyankin ◽  
S.V. Golodukhina ◽  
...  

2017 ◽  
Vol 36 (3) ◽  
pp. 822-828
Author(s):  
SG Bawa ◽  
AS Ahmed ◽  
PC Okonkwo

Thermal stability of transitional alumina phases produced from ammonium alum using Kankara kaolin as starting material was studied. Wet beneficiation method was employed to purify the starting material, after which it was calcined and dealuminated with sulphuric acid. The elemental composition, mineralogical, and physiological analyses were carried out using X-ray fluorescence (XRF), X-ray diffraction (XRD) and Brunauer-Emmett-Teller (BET) techniques respectively. The ammonium alum was thermally treated by varying the calcination temperature from 700 to 1200°C and varying the time of calcination from 1 to 4 h. The formation of gamma alumina began at calcination temperature of 825°C for calcination time of 3 h, which was found to be lower than reported works of 900°C. It was found to be stable at higher temperature of 1125°C, above which phase transformation to alpha alumina was observed. The observed wide range of thermal stability of the gamma alumina phase gives it good advantage to be used for high temperature applications, such as support for catalyst promoters. Alpha alumina phase formation began at 1150°C and was fully formed at 1200°C. BET specific surface area of 166 m2/g was obtained for the gamma alumina phase which was high enough for it application as support for catalyst, catalyst and adsorbent. http://dx.doi.org/10.4314/njt.v36i3.23


RSC Advances ◽  
2016 ◽  
Vol 6 (42) ◽  
pp. 35340-35347 ◽  
Author(s):  
Dongwei Li ◽  
Hui Wang ◽  
Chunying Shi ◽  
Xiaohong Xu

An unsupported dealloyed bimodal nanoporous PtCo alloy exhibited significantly improved catalytic activity and stability for CO oxidation.


2017 ◽  
Vol 43 (11) ◽  
pp. 6187-6205
Author(s):  
Yue Zhou ◽  
Xin Liu ◽  
Qiulin Zhang ◽  
Qixian Liu ◽  
Zhongxian Song ◽  
...  

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