COBALT OXIDE DECORATED FLOWER-LIKE g-C3N4 HYBRID NANOMATERIALS FOR CARBON MONOXIDE OXIDATION

2016 ◽  
Vol 24 (05) ◽  
pp. 1750058 ◽  
Author(s):  
YAN WANG ◽  
JING HUANG ◽  
JIANLIANG CAO ◽  
GAOJIE LI ◽  
ZHANYING ZHANG

Co3O4 decorated flower-like g-C3N4 hybrid nanocatalysts were successfully synthesized and prepared via a facial hydrothermal method. The composition and morphology of the as-synthesized Co3O4/g-C3N4 nanocatalysts were characterized by the techniques of XRD, FT-IR, SEM, TEM, XPS and N2-sorption. The analysis results indicated that the as-synthesized samples possess the flower-like structure, which consisted of g-C3N4 nanosheets and Co3O4 nanoparticles with the size about 25[Formula: see text]nm. The as-prepared Co3O4/g-C3N4 catalysts possess high catalytic activity and excellent stability for carbon monoxide (CO) oxidation. The total conversion of Co can be kept for more than 48[Formula: see text]h under the reaction temperature of 120[Formula: see text]C.

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.


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

1995 ◽  
Vol 24 (8) ◽  
pp. 699-700 ◽  
Author(s):  
Tsutomu Suzuki ◽  
Yuzo Imizu ◽  
Yoshinobu Satoh ◽  
Sunao Ozaki

2021 ◽  
Author(s):  
Ruixue Wang ◽  
Ying Yue ◽  
Huiying Wei ◽  
Jinxin Guo ◽  
Yanzhao Yang

Here, a novel synthetic route of ceria-based nanocatalysts with high catalytic activity and excellent stability was constructed by utilizing function groups from surface ligands. The surface of ceria nanorods were...


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

RSC Advances ◽  
2016 ◽  
Vol 6 (96) ◽  
pp. 93985-93996 ◽  
Author(s):  
Yanan Tang ◽  
Jincheng Zhou ◽  
Zigang Shen ◽  
Weiguang Chen ◽  
Chenggang Li ◽  
...  

The geometric, electronic and catalytic characters of Fe atom embedded graphene (including monovacancy and divacancy) are investigated using the first-principles method, which gives a reference on designing graphene-based catalysts for CO oxidation.


2021 ◽  
Author(s):  
Xiaoying Gao ◽  
Xuan Xie ◽  
Kanjun Sun ◽  
Xiaofei Lei ◽  
Tianyu Hou ◽  
...  

Fe, N co-doped carbon electrocatalyst is one of the most attractive alternatives to Pt/C catalysts due to its high catalytic activity, excellent stability and low cost. However, obtaining stable and...


Catalysts ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 1078
Author(s):  
Hang Zhang ◽  
Zhipeng Ma ◽  
Yunpeng Min ◽  
Huiru Wang ◽  
Ru Zhang ◽  
...  

Several kinds of composite materials with phosphotungstic acid (PTA) as the catalyst were prepared with activated carbon as support, and their structures were characterized. According to the Box–Behnken central combination principle, the mathematical model of the heterogeneous system is established. Based on the single-factor experiments, the reaction temperature, the reaction time, the amount of hydrogen peroxide and the loading capacity of PTA were selected as the influencing factors to study the catalyzed oxidation of hydrogen peroxide and degradation of high molecular weight chitosan. The results of IR showed that the catalyst had a Keggin structure. The results of the mercury intrusion test showed that the pore structure of the supported PTA catalyst did not change significantly, and with the increase of PTA loading, the porosity and pore volume decreased regularly, which indicated that PTA molecules had been absorbed and filled into the pore of activated carbon. The results of Response Surface Design (RSD) showed that the optimum reaction conditions of supported PTA catalysts for oxidative degradation of high molecular weight chitosan by hydrogen peroxide were as follows: reaction temperature was 70 ℃, reaction time was 3.0 h, the ratio of hydrogen peroxide to chitosan was 2.4 and the catalyst loading was 30%. Under these conditions, the yield and molecular weight of water-soluble chitosan were 62.8% and 1290 Da, respectively. The supported PTA catalyst maintained high catalytic activity after three reuses, which indicated that the supported PTA catalyst had excellent catalytic activity and stable performance compared with the PTA catalyst.


Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 252 ◽  
Author(s):  
Gabriela Dobras ◽  
Kornela Kasperczyk ◽  
Sebastian Jurczyk ◽  
Beata Orlińska

N-Hydroxyphthalimide was immobilized via ester bond on commercially available silica gel (SiOCONHPI) and then coated with various ionic liquids containing dissolved CoCl2 (SiOCONHPI@CoCl2@IL). New catalysts were characterized by means of FT IR spectroscopy, elemental analysis, SEM and TGA analysis and used in ethylbenzene oxidation with oxygen under mild solvent-free conditions (80 °C, 0.1 MPa). High catalytic activity of SiOCONHPI was proved. In comparison to a non-catalytic reaction, a two-fold increase in conversion of ethylbenzene was observed (from 4.7% to 8.6%). Coating of SiOCONHPI with [bmim][OcOSO3], [bmim][Cl] and [bmim][CF3SO3] containing CoCl2 enabled to increase the catalytic activity in relation to systems in which IL and CoCl2 were added directly to reaction mixture. The highest conversion of ethylbenzene was obtained while SiOCONHPI@CoCl2@[bmim][OcOSO3] were used (12.1%). Catalysts recovery and reuse was also studied.


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