Cobalt–magnesia catalyst by oxalate co-precipitation method for dry reforming of methane under pressure

2004 ◽  
Vol 5 (12) ◽  
pp. 771-775 ◽  
Author(s):  
K. Omata ◽  
N. Nukui ◽  
T. Hottai ◽  
M. Yamada
Catalysts ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 750 ◽  
Author(s):  
Ali M. A. Al-Najar ◽  
Faris A. J. Al-Doghachi ◽  
Ali A. A. Al-Riyahee ◽  
Yun Hin Taufiq-Yap

Pt,Pd,Ni/MgO, Pt,Pd,Ni/Mg0.97La3+0.03O, Pt,Pd,Ni/Mg0.93La3+0.07O, and Pt,Pd,Ni/Mg0.85La3+0.15O (1% of each of the Ni, Pd, and Pt) catalysts were prepared by a surfactant-assisted co-precipitation method. Samples were characterized by the XRD, XPS, XRF, FT-IR, H2-TPR, TEM, the Brunauer–Emmett–Teller (BET) method, and TGA and were tested for the dry reforming of methane (DRM). TEM and thermal gravimetric analysis (TGA) methods were used to analyze the carbon deposition on spent catalysts after 200 h at 900 °C. At a temperature of 900 °C and a 1:1 CH4:CO2 ratio, the tri-metallic Pt,Pd,Ni/Mg0.85La3+0.15O catalyst with a lanthanum promoter showed a higher conversion of CH4 (85.01%) and CO2 (98.97%) compared to the Ni,Pd,Pt/MgO catalysts in the whole temperature range. The selectivity of H2/CO decreased in the following order: Pt,Pd,Ni/Mg0.85La3+0.15O > Pt,Pd,Ni/Mg0.93La3+0.07O > Pt,Pd,Ni/Mg0.97La3+0.03O > Ni,Pd,Pt/MgO. The results indicated that among the catalysts, the Pt,Pd,Ni/Mg0.85La23+0.15O catalyst exhibited the highest activity, making it the most suitable for the dry reforming of methane reaction.


2021 ◽  
Vol 880 (1) ◽  
pp. 012035
Author(s):  
Z Abdelsadek ◽  
P Chaudhari ◽  
J P Holgado ◽  
F Bali ◽  
D Halliche ◽  
...  

Abstract Co0.67Al0.31 and Co0.14Mg0.54Al0.31 hydrotalcite based catalysts were prepared by a co-precipitation method at a fixed pH=11, exhibiting a suitable hydrotalcite structure to be used as a catalyst in the reaction of the dry reforming of methane (DRM). Calcination at 450 °C provides the best conditions to prepare the most adapted structure and morphology to be later used in the DRM reaction. The samples were characterised by XRD, FTIR, SEM and it was shown that they exhibit a specific surface in the 30-70 g/cm2 and a crystallite size of approximately 20 nm. The results of the TPR analysis showed clearly that CoAl-HT has better catalytic performances than CoMgAl-HT. This result can be explained by the presence of the Co0 for the catalyst CoAl-HTc-R and the total absence in the sample CoMgAl-HTc-R. The solid CoMgAl-HTc-R requires high reduction temperature compared to CoAl-HTc-R due to the strong CoO-MgO interactions.


2018 ◽  
Vol 554 ◽  
pp. 95-104 ◽  
Author(s):  
Jinni Xin ◽  
Hongjie Cui ◽  
Zhenmin Cheng ◽  
Zhiming Zhou

2015 ◽  
Vol 31 (5) ◽  
pp. 948-954 ◽  
Author(s):  
ZHANG Xiao-Qing ◽  
◽  
XU Yan YAN ◽  
YANG Chun-Hui ◽  
ZHANG Yan-Ping ◽  
...  

2017 ◽  
Vol 34 (11) ◽  
pp. 2823-2831 ◽  
Author(s):  
Qiulin Zhang ◽  
Jing Wang ◽  
Ping Ning ◽  
Tengfei Zhang ◽  
Mingzhi Wang ◽  
...  

Catalysts ◽  
2019 ◽  
Vol 10 (1) ◽  
pp. 27 ◽  
Author(s):  
Eswaravara Prasadarao Komarala ◽  
Ilia Komissarov ◽  
Brian A. Rosen

Perovskites LaNi0.8Fe0.2O3 and LaNi0.8Mn0.2O3 were synthesized using the co-precipitation method by substituting 20 mol.% of the Ni-site with Fe and Mn, respectively. Temperature programmed reduction (TPR) showed that the exsolution process in the Fe- and Mn-substituted perovskites followed a two-step and three-step reduction pathway, respectively. Once exsolved, the catalysts were found to be able to regenerate the original perovskite when exposed to an oxygen environment but with different crystallographic properties. The catalytic activity for both materials after exsolution was measured for the methane dry reforming (DRM) reaction at 650 °C and 800 °C. Catalyst resistance against nickel agglomeration, unwanted phase changes, and carbon accumulation during DRM were analyzed using X-ray diffraction (XRD), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA). The presence Fe alloying in the catalyst particles after exsolution from LaNi0.8Fe0.2O3 led to a lower methane conversion compared to the catalyst derived from LaNi0.8Mn0.2O3 where no alloying occurred.


2015 ◽  
Vol 7 (2) ◽  
pp. 1393-1403
Author(s):  
Dr R.P VIJAYALAKSHMI ◽  
N. Manjula ◽  
S. Ramu ◽  
Amaranatha Reddy

Single crystalline nano-sized multiferroic BiFeO3 (BFO) powders were synthesized through simple chemical co-precipitation method using polyethylene glycol (PEG) as capping agent. We obtained pure phase BiFeO3 powder by controlling pHand calcination temperature. From X-ray diffraction studies the nanoparticles were unambiguously identified to have a rhombohedrally distorted perovskite structure belonging to the space group of R3c. No secondary phases were detected. It indicates single phase structure. EDX spectra indicated the appearance of three elements Bi, Fe, O in 1:1:3. From the UV-Vis diffuse reflectance spectrum, the absorption cut-off wavelength of the BFO sample is around 558nm corresponding to the energy band gap of 2.2 eV. The size (60-70 nm) and morphology of the nanoparticles have been analyzed using transmission electron microscopy (TEM).   Linear M−H behaviour and slight hysteresis at lower magnetic field is observed for BiFeO3 nanoparticles from Vibrating sample magnetometer studies. It indicates weak ferromagnetic behaviour at room temperature. From dielectric studies, the conductivity value is calculated from the relation s = L/RbA Sm-1 and it is around 7.2 x 10-9 S/m.


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