Effect of Catalyst (de)activation on Reagent Diffusion in ZSM-5/alumina Extruded Pellet for the Methanol-to-hydrocarbons Conversion

Author(s):  
Alexey A. Zhokh

Abstract A pelletized ZSM-5/alumina catalyst was prepared by the extrusion technique. The catalyst was activated by ion-exchange with NH4NO3 aqueous solution. The activated catalyst was trained in the methanol-to-hydrocarbons reaction which caused the catalyst deactivation due to coke deposition (6.5 % wt.). Coke deposition resulted in a two-time decrease in the micropore volume. The methane, benzene, and methanol transport through ZSM-5/alumina pellet were consequently studied prior to activation, after activation, and after catalyst deactivation. A slight decrease in the diffusion rate after catalyst activation is observed. After deactivation, the diffusion rate increases insignificantly. The diffusion regime remains unchanged with respect to either activation or deactivation procedure. Contrary, for the methanol, the diffusion rate through a deactivated catalyst pellet remarkably increases due to micropore blockage by coke deposition. The obtained results reveal that the micropores blockage during the catalyst deactivation enhances the methanol mass transfer.

1985 ◽  
Vol 50 (11) ◽  
pp. 2381-2395
Author(s):  
Alena Brunovská ◽  
Ján Buriánek ◽  
Ján Ilavský ◽  
Ján Valtýni

The diffusion and the shell progressive models of deactivation caused by irreversible chemisorption of a catalytic poison are presented for a single catalyst pellet. The method for solution of the model equations is proposed. The numerical results are compared with experimental data obtained by measuring concentration and temperature changes due to thiophene poisoning in benzene hydrogenation over a nickel-alumina catalyst.


2010 ◽  
Vol 275 (1) ◽  
pp. 170-180 ◽  
Author(s):  
Morten Bjørgen ◽  
Sema Akyalcin ◽  
Unni Olsbye ◽  
Sandrine Benard ◽  
Stein Kolboe ◽  
...  

1985 ◽  
Vol 34 (1-6) ◽  
pp. 363-374 ◽  
Author(s):  
TAKESHIGE TAKAHASHI ◽  
MCHIAKI NOMURA ◽  
MASASHI TASHIRO

Energies ◽  
2021 ◽  
Vol 15 (1) ◽  
pp. 53
Author(s):  
Kai Miao ◽  
Tan Li ◽  
Jing Su ◽  
Cong Wang ◽  
Kaige Wang

Catalytic hydropyrolysis via the introduction of external hydrogen into catalytic pyrolysis process using hydrodeoxygenation catalysts is one of the major approaches of bio-oil upgrading. In this study, hydrodeoxygenation of acetone over Mo/HZSM-5 and HZSM-5 were investigated with focus on the influence of hydrogen pressure and catalyst deactivation. It is found that doped MoO3 could prolong the catalyst activity due to the suppression of coke formation. The influence of hydrogen pressure on catalytic HDO of acetone was further studied. Hydrogen pressure of 30 bar effectively prolonged catalyst activity while decreased the coke deposition over catalyst. The coke formation over the HZSM-5 and Mo/HZSM-5 under 30 bar hydrogen pressure decreased 66% and 83%, respectively, compared to that under atmospheric hydrogen pressure. Compared to the test with the HZSM-5, 35% higher yield of aliphatics and 60% lower coke were obtained from the Mo/HZSM-5 under 30 bar hydrogen pressure. Characterization of the spent Mo/HZSM-5 catalyst revealed the deactivation was mainly due to the carbon deposition blocking the micropores and Bronsted acid sites. Mo/HZSM-5 was proved to be potentially enhanced production of hydrocarbons.


2019 ◽  
Vol 63 (3-4) ◽  
pp. 268-280 ◽  
Author(s):  
Abarasi Hart ◽  
Mohamed Adam ◽  
John P. Robinson ◽  
Sean P. Rigby ◽  
Joseph Wood

AbstractThe Toe-to-Heel Air Injection (THAI) combined with a catalytic add-on (CAPRI, CATalytic upgrading PRocess In-situ) have been a subject of investigation since 2002. The major challenges have been catalyst deactivation due to coke deposition and low temperatures (~ 300 °C) of the mobilised hot oil flowing over the catalyst packing around the horizontal well. Tetralin has been used to suppress coke formation and also improve upgraded oil quality due to its hydrogen-donor capability. Herein, inductive heating (IH) incorporated to the horizontal production well is investigated as one means to resolve the temperature shortfall. The effect of reaction temperature on tetralin dehydrogenation and hydrogen evolution over NiMo/Al2O3 catalyst at 250–350 °C, catalyst-to-steel ball ratio (70% v/v), 18 bar and 0.75 h−1 was investigated. As temperature increased from 250 to 350 °C, tetralin conversion increased from 40 to 88% while liberated hydrogen increased from 0.36 to 0.88 mol based on 0.61 mol of tetralin used. The evolved hydrogen in situ hydrogenated unreacted tetralin to trans and cis-decalins with the selectivity of cis-decalin slightly more at 250 °C while at 300–350 °C trans-decalin showed superior selectivity. With IH the catalyst bed temperature was closer to the desired temperature (300 °C) with a mean of 299.2 °C while conventional heating is 294.3 °C. This thermal advantage and the nonthermal effect from electromagnetic field under IH improved catalytic activity and reaction rate, though coke formation increased.


ACS Catalysis ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 7065-7072 ◽  
Author(s):  
Brandon L. Foley ◽  
Blake A. Johnson ◽  
Aditya Bhan

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