scholarly journals Molecular coupling behavior of relay catalytic upgrading of heavy oil fast pyrolysis vapor to produce light olefins

Author(s):  
Yuanjun Che ◽  
Kunmou Shi ◽  
Qian Wang ◽  
Ruiyuan Tang ◽  
Yuanyu Tian
2019 ◽  
Vol 137 ◽  
pp. 259-265 ◽  
Author(s):  
Mingfa Yang ◽  
Jingai Shao ◽  
Zixu Yang ◽  
Haiping Yang ◽  
Xianhua Wang ◽  
...  

2019 ◽  
Vol 98 (10) ◽  
pp. 254-258 ◽  
Author(s):  
Nichaboon CHAIHAD ◽  
Surachai KARNJANAKOM ◽  
Irwan KURNIA ◽  
Akihiro YOSHIDA ◽  
Abuliti ABUDULA ◽  
...  

Energies ◽  
2019 ◽  
Vol 12 (18) ◽  
pp. 3474 ◽  
Author(s):  
Yichen Liu ◽  
James J. Leahy ◽  
Jacek Grams ◽  
Witold Kwapinski

Fast pyrolysis of Miscanthus, its hydrolysis residue and lignin were carried with a pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) followed by online vapor catalytic upgrading with sulfated ZrO2, sulfated TiO2 and sulfated 60 wt.% ZrO2-TiO2. The most evident influence of the catalyst on the vapor phase composition was observed for aromatic hydrocarbons, light phenols and heavy phenols. A larger amount of light phenols was detected, especially when 60 wt.% ZrO2-TiO2 was present. Thus, a lower average molecular weight and lower viscosity of bio-oil could be obtained with this catalyst. Pyrolysis was also performed at different pressures of hydrogen. The pressure of H2 has a great effect on the overall yield and the composition of biomass vapors. The peak area percentages of both aromatic hydrocarbons and cyclo-alkanes are enhanced with the increasing of H2 pressure. The overall yields are higher with the addition of either H2 or sulfated catalysts. This is beneficial as phenols are valuable chemicals, thus, increasing the value of bio-oil. The results show that the hydrolysis residue has the potential to become a resource for phenol production.


2020 ◽  
Vol 60 (3) ◽  
pp. 384-391
Author(s):  
N. N. Sviridenko ◽  
A. V. Vosmerikov ◽  
M. R. Agliullin ◽  
B. I. Kutepov

Catalysts ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 497 ◽  
Author(s):  
Abarasi Hart ◽  
Mohamed Adam ◽  
John P. Robinson ◽  
Sean P. Rigby ◽  
Joseph Wood

This paper reports the hydrogenation and dehydrogenation of tetralin and naphthalene as model reactions that mimic polyaromatic compounds found in heavy oil. The focus is to explore complex heavy oil upgrading using NiMo/Al2O3 and CoMo/Al2O3 catalysts heated inductively with 3 mm steel balls. The application is to augment and create uniform temperature in the vicinity of the CAtalytic upgrading PRocess In-situ (CAPRI) combined with the Toe-to-Heel Air Injection (THAI) process. The effect of temperature in the range of 210–380 °C and flowrate of 1–3 mL/min were studied at catalyst/steel balls 70% (v/v), pressure 18 bar, and gas flowrate 200 mL/min (H2 or N2). The fixed bed kinetics data were described with a first-order rate equation and an assumed plug flow model. It was found that Ni metal showed higher hydrogenation/dehydrogenation functionality than Co. As the reaction temperature increased from 210 to 300 °C, naphthalene hydrogenation increased, while further temperature increases to 380 °C caused a decrease. The apparent activation energy achieved for naphthalene hydrogenation was 16.3 kJ/mol. The rate of naphthalene hydrogenation was faster than tetralin with the rate constant in the ratio of 1:2.5 (tetralin/naphthalene). It was demonstrated that an inductively heated mixed catalytic bed had a smaller temperature gradient between the catalyst and the surrounding fluid than the conventional heated one. This favored endothermic tetralin dehydrogenation rather than exothermic naphthalene hydrogenation. It was also found that tetralin dehydrogenation produced six times more coke and caused more catalyst pore plugging than naphthalene hydrogenation. Hence, hydrogen addition enhanced the desorption of products from the catalyst surface and reduced coke formation.


2019 ◽  
Vol 143 ◽  
pp. 104684
Author(s):  
Xiao-Dong Tang ◽  
Tian-Da Zhou ◽  
Jing-Jing Li ◽  
Chang-Lian Deng ◽  
Guang-Fu Qin

1999 ◽  
Vol 38 (13) ◽  
Author(s):  
R.G. Moore ◽  
C.J. Laureshen ◽  
S.A. Mehta ◽  
M.G. Ursenbach ◽  
J.D.M. Belgrave ◽  
...  

2014 ◽  
Vol 61 ◽  
pp. 1937-1941 ◽  
Author(s):  
Qiang Lu ◽  
Zhi-bo Zhang ◽  
Xiao-qiang Wang ◽  
Chang-qing Dong ◽  
Yong-qian Liu

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