scholarly journals Preparation and High-Throughput Testing of TiO2-Supported Co Catalysts for Fischer‒Tropsch Synthesis

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 352
Author(s):  
Christian Schulz ◽  
Peter Kolb ◽  
Dennis Krupp ◽  
Lars Ritter ◽  
Alfred Haas ◽  
...  

A series of Co/TiO2 catalysts was tested in a parameters field study for Fischer‒Tropsch synthesis (FTS). All catalysts were prepared by the conventional impregnation technique to obtain an industrially relevant Co content of 10 wt % or 20 wt %, respectively. In summary, 10 different TiO2 of pure anatase phase, pure rutile phase, as well as mixed rutile and anatase phase were used as supports. Performance tests were conducted with a 32-fold high-throughput setup for accelerated catalyst benchmarking; thus, 48 experiments were completed within five weeks in a relevant operation parameters field (170 °C to 233.5 °C, H2/CO ratio 1 to 2.5, and 20 bar(g)). The most promising catalyst showed a CH4 selectivity of 5.3% at a relevant CO conversion of 60% and a C5+ productivity of 2.1 gC5+/(gCo h) at 207.5 °C. These TiO2-based materials were clearly differentiated with respect to the application as supports in Co-catalyzed FTS catalysis. The most prospective candidates are available for further FTS optimization at a commercial scale.

Fuel ◽  
2021 ◽  
Vol 293 ◽  
pp. 120435
Author(s):  
Dalia Liuzzi ◽  
Francisco J. Pérez-Alonso ◽  
Sergio Rojas

Catalysts ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 732
Author(s):  
José Antonio Díaz-López ◽  
Jordi Guilera ◽  
Martí Biset-Peiró ◽  
Dan Enache ◽  
Gordon Kelly ◽  
...  

The present work explores the technical feasibility of passivating a Co/γ-Al2O3 catalyst by atomic layer deposition (ALD) to reduce deactivation rate during Fischer–Tropsch synthesis (FTS). Three samples of the reference catalyst were passivated using different numbers of ALD cycles (3, 6 and 10). Characterization results revealed that a shell of the passivating agent (Al2O3) grew around catalyst particles. This shell did not affect the properties of passivated samples below 10 cycles, in which catalyst reduction was hindered. Catalytic tests at 50% CO conversion evidenced that 3 and 6 ALD cycles increased catalyst stability without significantly affecting the catalytic performance, whereas 10 cycles caused blockage of the active phase that led to a strong decrease of catalytic activity. Catalyst deactivation modelling and tests at 60% CO conversion served to conclude that 3 to 6 ALD cycles reduced Co/γ-Al2O3 deactivation, so that the technical feasibility of this technique was proven in FTS.


2012 ◽  
Vol 25 ◽  
pp. 12-17 ◽  
Author(s):  
Muthu Kumaran Gnanamani ◽  
Gary Jacobs ◽  
Wilson D. Shafer ◽  
Mauro C. Ribeiro ◽  
Venkat Ramana Rao Pendyala ◽  
...  

Symmetry ◽  
2018 ◽  
Vol 10 (11) ◽  
pp. 572 ◽  
Author(s):  
Omid Akbarzadeh ◽  
Noor Mohd Zabidi ◽  
Yasmin Abdul Wahab ◽  
Nor Hamizi ◽  
Zaira Chowdhury ◽  
...  

Pre-treating the multi-walled carbon nanotubes (CNTs) support by refluxing in 35 vol% nitric acid followed by heating at the temperature of 600 to 900 °C resulted in the formation of defects on the CNTs. Increasing the temperature of the pre-treatment of the CNTs from 600 °C to 900 °C, enhanced the fraction of cobalt-oxide nanoparticles encapsulated in the channels of CNTs from 31% to 70%. The performance of Co/CNTs in Fischer-Tropsch synthesis (FTS) was evaluated in a fixed-bed micro-reactor at a temperature of 240 °C and a pressure of 2.0 MPa. The highest CO conversion obtained over Co/CNTs.A.900 was 59% and it dropped by ~3% after 130 h of time-on-stream. However, maximum CO conversion using Co/CNTs.A.600 catalysts was 28% and it decreased rapidly by about 54% after 130 h of time-on-stream. These findings show that the combined acid and thermal pre-treatment of CNTs support at 900 °C has improved the stability and activity of the Co/CNTs catalyst in FTS.


2012 ◽  
Vol 142 (11) ◽  
pp. 1382-1387 ◽  
Author(s):  
Dragomir B. Bukur ◽  
Zhendong Pan ◽  
Wenping Ma ◽  
Gary Jacobs ◽  
Burtron H. Davis

2014 ◽  
Vol 470 ◽  
pp. 250-260 ◽  
Author(s):  
Jia Yang ◽  
Wenping Ma ◽  
De Chen ◽  
Anders Holmen ◽  
Burtron H. Davis

2013 ◽  
Vol 215 ◽  
pp. 121-130 ◽  
Author(s):  
Jun Zhu ◽  
Jia Yang ◽  
Andreas Helland Lillebø ◽  
Ye Zhu ◽  
Yingda Yu ◽  
...  

Catalysts ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 553 ◽  
Author(s):  
Karolina A. Chalupka ◽  
Jacek Grams ◽  
Pawel Mierczynski ◽  
Malgorzata I. Szynkowska ◽  
Jacek Rynkowski ◽  
...  

A goal of this work was to investigate the influence of the preparation procedure and activation conditions (reduction temperature and reducing medium: pure hydrogen (100% H2) or hydrogen-argon mixture (5% H2-95% Ar)) on the activity of Co-containing BEA zeolites in Fischer–Tropsch synthesis. Therefore, a series of CoBEA zeolites were obtained by a conventional wet impregnation (Co5.0AlBEA) and a two-step postsynthesis preparation procedure involving dealumination and impregnation steps (Co5.0SiBEA). Both types of zeolites were calcined in air at 500 °C for 3 h and then reduced at 500, 800 and 900 °C for 1 h in 100 % H2 and in 5% H2–95% Ar mixture flow. The obtained Red-C-Co5.0AlBEA and Red-C-Co5.0SiBEA catalysts with various physicochemical properties were tested in Fischer–Tropsch reaction. Among the studied catalysts, Red-C-Co5.0SiBEA reduced at 500 °C in pure hydrogen was the most active, presenting selectivity to liquid products of 91% containing mainly C7–C16 n-alkanes and isoalkanes as well as small amount of olefins, with CO conversion of about 11%. The Red-C-Co5.0AlBEA catalysts were not active in the Fischer–Tropsch synthesis. It showed that removal of aluminum from the BEA zeolite in the first step of postsynthesis preparation procedure played a key role in the preparation of efficient catalysts for Fischer–Tropsch synthesis. An increase of the reduction temperature from 500 to 800 and 900 °C resulted in two times lower CO conversion and a drop of the selectivity towards liquid products (up to 62%–88%). The identified main liquid products were n-alkanes and isoalkanes. The higher activity of Red-C-Co5.0SiBEA catalysts can be assigned to good dispersion of cobalt nanoparticles and thus a smaller cobalt nanoparticles size than in the case of Red-C-Co5.0AlBEA catalyst.


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