Kinetic model considering catalyst deactivation for the steam reforming of bio-oil over Ni/La2O3-αAl2O3

2018 ◽  
Vol 332 ◽  
pp. 192-204 ◽  
Author(s):  
Ana G. Gayubo ◽  
Beatriz Valle ◽  
Borja Aramburu ◽  
Carolina Montero ◽  
Javier Bilbao
2014 ◽  
Vol 471 ◽  
pp. 118-125 ◽  
Author(s):  
Srinivas Appari ◽  
Vinod M. Janardhanan ◽  
Ranjit Bauri ◽  
Sreenivas Jayanti ◽  
Olaf Deutschmann

Author(s):  
Yishuang Wang ◽  
Mingqiang Chen ◽  
Tian Liang ◽  
Jie Yang ◽  
Zhonglian Yang ◽  
...  

In this research, catalytic steam reforming acetic acid derived from the aqueous portion of bio-oil for hydrogen production was investigated by using different Ni/ATC (Attapulgite Clay) catalysts prepared by precipitation, impregnation and mechanical blending methods. The fresh and reduced catalysts were characterized by XRD, N2 adsorption-desorption, TEM and H2-TPR. The comprehensive results demonstrated that the interaction between active metallic Ni and ATC carrier was significantly improved in Ni/ATC catalyst prepared by precipitation method, and in which the mean Ni particle size was the smallest (~13 nm) resulted in the highest metal dispersion (7.5%). The catalytic performance of the three catalysts was evaluated through the process of steam reforming of acetic acid in a fixed-bed reactor under atmospheric pressure at two different temperatures, such as 550 ℃ and 650 ℃. Results showed that the Ni/ATC (PM-N/ATC) prepared by precipitation method, achieved the highest H2 yield of ~82% and little lower acetic acid conversion efficiency of ~85% than that (~95%) of Ni/ATC (IM-NATC) prepared by impregnation method. In addition, the deactivation catalysts after reaction for 4 h were analyzed by XRD, TGA-DTG and TEM, which demonstrated that the catalyst deactivation was not caused by the amount of carbon deposition, but owed to the significant agglomeration and sintering of Ni particles in the carrier.


2013 ◽  
Vol 115 ◽  
pp. 222-232 ◽  
Author(s):  
Aingeru Remiro ◽  
Beatriz Valle ◽  
A.T. Aguayo ◽  
Javier Bilbao ◽  
Ana G. Gayubo

Fuel ◽  
2018 ◽  
Vol 216 ◽  
pp. 463-474 ◽  
Author(s):  
Beatriz Valle ◽  
Borja Aramburu ◽  
Martin Olazar ◽  
Javier Bilbao ◽  
Ana G. Gayubo

Author(s):  
Mira Abou Rjeily ◽  
Cédric Gennequin ◽  
Hervé Pron ◽  
Edmond Abi-Aad ◽  
Jaona Harifidy Randrianalisoa

Energies ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1875
Author(s):  
Prashanth Reddy Buchireddy ◽  
Devin Peck ◽  
Mark Zappi ◽  
Ray Mark Bricka

Amongst the issues associated with the commercialization of biomass gasification, the presence of tars has been one of the most difficult aspects to address. Tars are an impurity generated from the gasifier and upon their condensation cause problems in downstream equipment including plugging, blockages, corrosion, and major catalyst deactivation. These problems lead to losses of efficiency as well as potential maintenance issues resulting from damaged processing units. Therefore, the removal of tars is necessary in order for the effective operation of a biomass gasification facility for the production of high-value fuel gas. The catalytic activity of montmorillonite and montmorillonite-supported nickel as tar removal catalysts will be investigated in this study. Ni-montmorillonite catalyst was prepared, characterized, and tested in a laboratory-scale reactor for its efficiency in reforming tars using naphthalene as a tar model compound. Efficacy of montmorillonite-supported nickel catalyst was tested as a function of nickel content, reaction temperature, steam-to-carbon ratio, and naphthalene loading. The results demonstrate that montmorillonite is catalytically active in removing naphthalene. Ni-montmorillonite had high activity towards naphthalene removal via steam reforming, with removal efficiencies greater than 99%. The activation energy was calculated for Ni-montmorillonite assuming first-order kinetics and was found to be 84.5 kJ/mole in accordance with the literature. Long-term activity tests were also conducted and showed that the catalyst was active with naphthalene removal efficiencies greater than 95% maintained over a 97-h test period. A little loss of activity was observed with a removal decrease from 97% to 95%. To investigate the decrease in catalytic activity, characterization of fresh and used catalyst samples was performed using thermogravimetric analysis, transmission electron microscopy, X-ray diffraction, and surface area analysis. The loss in activity was attributed to a decrease in catalyst surface area caused by nickel sintering and coke formation.


2011 ◽  
Vol 25 (7) ◽  
pp. 3289-3297 ◽  
Author(s):  
Pedro J. Ortiz-Toral ◽  
Justinus Satrio ◽  
Robert C. Brown ◽  
Brent H. Shanks

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