Effect of Fe and Co promoters on CO methanation activity of nickel catalyst prepared by impregnation – co-precipitation method

Author(s):  
Buyan-Ulzii Battulga ◽  
Tungalagtamir Bold ◽  
Enkhsaruul Byambajav

AbstractNi based catalysts supported on γ-Al2O3 that was unpromoted (Ni/γAl2O3) or promoted (Ni–Fe/γAl2O3, Ni–Co/γAl2O3, and Ni–Fe–Co/γAl2O3) were prepared using by the impregnation – co-precipitation method. Their catalytic performances for CO methanation were studied at 3 atm with a weight hourly space velocity (WHSV) of 3000 ml/g/h of syngas with a molar ratio of H2/CO = 3 and in the temperature range between 130 and 350 °C. All promoters could improve nickel distribution, and decreased its particle sizes. It was found that the Ni–Co/γAl2O3 catalyst showed the highest catalytic performance for CO methanation in a low temperature range (<250 °C). The temperatures for the 20% CO conversion over Ni–Co/γAl2O3, Ni–Fe/γAl2O3, Ni–Fe–Co/γAl2O3 and Ni/γAl2O3 catalysts were 205, 253, 263 and 270 °C, respectively. The improved catalyst distribution by the addition of cobalt promoter caused the formation of β type nickel species which had an appropriate interacting strength with alumina support in the Ni–Co/γAl2O3. Though an addition of iron promoter improved catalyst distribution, the methane selectivity was lowered due to acceleration of both CO methanation and WGS reaction with the Ni–Fe/γAl2O3. Moreover, it was found that there was no synergetic effect from the binary Fe–Co promotors in the Ni–Fe–Co/γAl2O3 on catalytic activity for CO methanation.

2016 ◽  
Vol 697 ◽  
pp. 279-283
Author(s):  
Yan Xia Wu ◽  
Hai Long Liang ◽  
Xin Chen ◽  
Jie Tang ◽  
Yu Feng Chen ◽  
...  

The catalytic performance of NO removal was studied over Mn-Ce/TiO2 catalysts prepared by different preparation parameters, such as preparation method, Ce/(Mn+Ce) molar ratio and calcination temperature. It was found that samples prepared by co-precipitation method, which had the largest surface area and highly dispersed active component particles, showed the best denitrification activity. The highest NO conversion of 95% is achieved at the Ce/(Mn+Ce) molar ratio of 15% which is much higher than that of the pure manganese constituent. The increase of calcining temperature favored the crystallization of active components, leading to the decline of catalytic activity.


Catalysts ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 900
Author(s):  
Imane Driouch ◽  
Weidong Zhang ◽  
Michèle Heitz ◽  
Jose Luis Valverde ◽  
Anne Giroir-Fendler

A series of Co3O4 catalysts were synthesized by an ammonia precipitation method at various precipitating pH values (8.0, 8.5, 9.0, 9.5, and 10.0) and with different numbers of washings. Their performance in the total oxidation of two selected hydrocarbons, toluene and propane, was evaluated at a reactant/oxygen molar ratio of 1/210 and a Weight Hourly Space Velocity (WHSV) of 40,000 mL g−1 h−1. The physicochemical properties of the catalysts were characterized by thermogravimetric and differential thermal analysis (TG/DTA), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD) and N2 absorption–desorption. The results show that the catalysts are in the cubic spinel phase (Fd-3m (227), a = 8.0840 Å) with average crystalline sizes of 29−40 nm and specific surface areas of 12–20 m2 g−1. All catalysts allowed 100% conversion of both toluene and propane at temperatures below 350 °C. The precipitating pH and the number of washings were observed to significantly affect the catalytic performance. The optimal synthesis condition was established to be pH 8.5 with two washings. The best catalyst gave 100% conversion of toluene and propane at 306 °C and 268 °C, respectively.


2011 ◽  
Vol 233-235 ◽  
pp. 1552-1555
Author(s):  
Yun Peng Zhao ◽  
Li Hua Jia ◽  
Tao Jing ◽  
De Zhi Sun ◽  
Jong Shik Chung

CuO-ZnO-ZrO2-TiO2 catalyst was prepared by parallel-slurry-mixing-precipitation method combined with addition of surfactant. The catalyst characterizations were investigated by Nitrogen adsorption-desorption, XRD, SEM and EDS. Results show that the average pore diameter of the mesoporous CuO-ZnO-ZrO2-TiO2 catalyst is 3.754 nm, and dispersion of CuOis better on CuO-ZnO-ZrO2-TiO2 catalyst. Under the conditions of reaction temperature of 503 K, reaction pressure of 2.0 MPa, space velocity of 2100 h-1 with a H2/CO2 molar ratio of 3:1, the catalyst exhibited favorable activity for methanol synthesis from CO2 hydrogenation. The selectivity to methanol and the yield of methanol were 27.42% and 4.50%, respectively.


2018 ◽  
Vol 41 (3-4) ◽  
pp. 73-89 ◽  
Author(s):  
Shengjia Wang ◽  
Zhiwei Tian ◽  
Qing Liu ◽  
Yingyun Qiao ◽  
Yuanyu Tian

Abstract To enhance the performance of anti-coking and anti-sintering of the Ni-based catalysts during the reaction process of CO methanation, we synthesized a group of catalysts denoted as “Ni-xMgAl2O4” via the modified co-precipitation method utilizing carbon black as hard template. The addition of carbon black could significantly improve the specific surface area of MgAl2O4 to 235.8 m2 g−1. The Ni catalysts supported on high-surface-area MgAl2O4 (Ni-0.25MA) exhibited enhanced catalytic performance and hydrothermal stability in comparison with the conventional Ni-based magnesia alumina spinel catalysts with the same NiO content. In the process of 120-h stability test, the Ni-0.25MA catalyst exhibited remarkable improvement in both anti-sintering and anti-coking. After a series of characterizations, we found that the addition of carbon black could make more pores over MgAl2O4, resulting in the supported Ni particles being anchored in the pore rather than on the outside surface of support. This structure enhanced the dispersion of nickel nanoparticles, thus strengthening the interaction between nickel species and the MgAl2O4 support, which led to the promotion in catalytic activity and stability of high-surface-area Ni/MgAl2O4.


Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 252
Author(s):  
Tadej Žumbar ◽  
Alenka Ristić ◽  
Goran Dražić ◽  
Hristina Lazarova ◽  
Janez Volavšek ◽  
...  

The structure–property relationship of catalytic supports for the deposition of redox-active transition metals is of great importance for improving the catalytic efficiency and reusability of the catalysts. In this work, the role of alumina support precursors of Cu-Fe/Al2O3 catalysts used for the total oxidation of toluene as a model volatile organic air pollutant is elucidated. Surface characterization of the catalysts revealed that the surface area, pore volume and acid site concentration of the alumina supports are important but not the determining factors for the catalytic activity of the studied catalysts for this type of reaction. The determining factors are the structural order of the support precursor, the homogeneous distribution of the catalytic sites and reducibility, which were elucidated by XRD, NMR, TEM and temperature programed reduction (TPR). Cu–Fe/Al2O3 prepared from bayerite and pseudoboehmite as highly ordered precursors showed better catalytic performance compared to Cu-Fe/Al2O3 derived from the amorphous alumina precursor and dawsonite. Homogeneous distribution of FexOy and CuOx with defined Cu/Fe molar ratio on the Al2O3 support is required for the efficient catalytic performance of the material. The study showed a beneficial effect of low iron concentration introduced into the alumina precursor during the alumina support synthesis procedure, which resulted in a homogeneous metal oxide distribution on the support.


Author(s):  
Ghazanfar Abbas ◽  
Rizwan Raza ◽  
Muhammad Ashraf Chaudhry ◽  
Bin Zhu

The entire world’s challenge is to find out the renewable energy sources due to rapid depletion of fossil fuels because of their high consumption. Solid Oxide Fuel Cells (SOFCs) are believed to be the best alternative source which converts chemical energy into electricity without combustion. Nanostructured study is required to develop highly ionic conductive electrolyte for SOFCs. In this work, the calcium doped ceria (Ce0.8Ca0.2O1.9) coated with 20% molar ratio of two alkali carbonates (CDC-M: MCO3, where M = Na and K) electrolyte was prepared by co-precipitation method in this study. Ni based electrode was used to fabricate the cell by dry pressing technique. The crystal structure and surface morphology was characterized by X-Ray Diffractometer (XRD), Scanning Electron Microscopy (SEM) and High Resolution Transmission Electron Microscopy (HRTEM). The particle size was calculated in the range of 10–20nm by Scherrer’s formula and compared with SEM and TEM results. The ionic conductivity was measured by using AC Electrochemical Impedance Spectroscopy (EIS) method. The activation energy was also evaluated. The performance of the cell was measured 0.567W/cm2 at temperature 550°C with hydrogen as a fuel.


2018 ◽  
Vol 281 ◽  
pp. 40-45
Author(s):  
Jie Guang Song ◽  
Lin Chen ◽  
Cai Liang Pang ◽  
Jia Zhang ◽  
Xian Zhong Wang ◽  
...  

YAG materials has a number of unique properties, the application is very extensive. In this paper, the superfine YAG powder materials were prepared by co-precipitation method and hydrothermal precipitation method. The influence of synthesis process on the morphology of the powder was investigated. The results showed that the precursor powder prepared via the co-precipitation method is mainly from amorphous to crystalline transition with the increasing calcination temperature, the precursor agglomeration is more serious, In the process of increasing the calcination temperature, the dispersibility of the roasted powder is greatly improved, which is favorable for the growth of the crystal grains, so that the particle size of the powder is gradually increased, the YAG precursor prepared by the co-precipitation method is transformed into YAG crystals, the phase transition occurs mainly between 900 and 1100°C. When the molar ratio of salt to alkali is Y3+: OH-=1: 8 via the hydrothermal reaction, the YAG particles with homogeneous morphology can be obtained. When the molar ratio of salt and alkali is increased continuously, the morphology of YAG particles is not obviously changed. The co-precipitation method is easy to control the particle size, the hydrothermal method is easy to control the particle morphology.


2015 ◽  
Vol 230 ◽  
pp. 153-159 ◽  
Author(s):  
Oksana Chukova ◽  
Sergiy G. Nedilko ◽  
Sergiy A. Nedilko ◽  
Tetiana Voitenko ◽  
Olga Gomenyuk ◽  
...  

The La1‑xEuxVO4 powders were synthesized by co-precipitation method. Emission spectra of the LaEuVO4 and La1‑xEuxVO4 powders consist of wide non-structural bands of the matrix emission and narrow spectral lines caused by inner f-f electron transitions in the Eu3+ ions, respectively. The both types of emission were studied within 8 – 300 K temperature range. Decomposition of spectra of the wide matrix emission on three bands has been carried out and temperature dependencies for each band were studied. Temperature behavior of the Eu3+ emission was investigated for lines assigned to different Eu3+ centres. Obtained dependencies are analyzed and discussed using proposed schemes of transitions in the VO43- groups and structure of the nearest surrounding of the Eu3+ emission centres.


2013 ◽  
Vol 781-784 ◽  
pp. 239-242
Author(s):  
Lei Wang ◽  
Peng Xiao

In this paper, SiMgAl hydotalcite synthesis conditions were investigated using co-precipitation method, within a relatively stable pH environment of 8~9. Our research, analysis and discussion focused on the effects of major factors, such as material molar ratio ,silicon content and aged condition, on the structures of synthetic products. To achieve stable and accurate data, synthetic products were characterized by XRD and IR under the identical conditions. As shown in the results, it is suggested that the best Crystallization temperature is 70°C, molar ratio of Mg to Al is 3:1, and the best content of Silicon is 0.015mol/mol.


Sign in / Sign up

Export Citation Format

Share Document