scholarly journals Synthesis, Characterisation and Water-Gas Shift Activity of Nano-Particulate Mixed-Metal (Al, Ti) Cobalt Oxides

Author(s):  
Moritz Wolf ◽  
Stephen J. Roberts ◽  
Ezra J. Olivier ◽  
Niels T. J. Luchters ◽  
Emma K. Gibson ◽  
...  

The formation of mixed-metal cobalt oxides, representing potential metal-support compounds for cobalt-based catalysts, has been observed at high conversion levels in the Fischer-Tropsch synthesis over metal oxide-supported cobalt catalysts. An often observed increase in the carbon dioxide selectivity at Fischer Tropsch conversion levels above 80% has been suggested to be inter-linked to the formation of water-gas shift active oxidic cobalt species. Mixed-metal cobalt oxides, namely cobalt aluminate and cobalt titanate, were therefore synthesised and tested for potential catalytic activity towards the water-gas shift reaction. We present a preparation route for amorphous mixed-metal oxides <i>via</i> thermal treatment of metal precursors in benzyl alcohol. Calcination of the as prepared nanoparticles results in highly crystalline phases. The nano-particulate mixed-metal cobalt oxides were thoroughly analysed by means of X-ray diffraction, Raman spectroscopy, temperature-programmed reduction, X-ray absorption near edge structure spectroscopy, and high-resolution scanning transmission electron microscopy. This complementary characterisation of the synthesised materials allows for a distinct identification of the phases and their properties. The cobalt aluminate prepared has a cobalt-rich composition (Co<sub>1+<i>x</i></sub>Al<sub>2-<i>x</i></sub>O<sub>4</sub>) with a homogeneous atomic distribution throughout the nano-particulate structures, while the perovskite-type cobalt titanate (CoTiO<sub>3</sub>) features cobalt-lean smaller particles being associated with larger ones with an increased concentration of cobalt. The cobalt aluminate prepared showed no water-gas shift activity in the medium-shift temperature range, while the cobalt titanate sample was shown to catalyse the conversion of water and carbon monoxide to hydrogen and carbon dioxide after an extended activation period. However, this perovskite underwent vast restructuring forming metallic cobalt, a known catalyst for the water-gas shift reaction at temperatures exceeding typical conditions for the cobalt-based Fischer-Tropsch synthesis, and anatase-TiO<sub>2</sub> <i>via</i> a partial reduction of the mixed-metal cobalt oxide and segregation as identified by means of post-run X-ray diffraction.

Author(s):  
Moritz Wolf ◽  
Stephen J. Roberts ◽  
Ezra J. Olivier ◽  
Niels T. J. Luchters ◽  
Emma K. Gibson ◽  
...  

The formation of mixed-metal cobalt oxides, representing potential metal-support compounds for cobalt-based catalysts, has been observed at high conversion levels in the Fischer-Tropsch synthesis over metal oxide-supported cobalt catalysts. An often observed increase in the carbon dioxide selectivity at Fischer Tropsch conversion levels above 80% has been suggested to be inter-linked to the formation of water-gas shift active oxidic cobalt species. Mixed-metal cobalt oxides, namely cobalt aluminate and cobalt titanate, were therefore synthesised and tested for potential catalytic activity towards the water-gas shift reaction. We present a preparation route for amorphous mixed-metal oxides <i>via</i> thermal treatment of metal precursors in benzyl alcohol. Calcination of the as prepared nanoparticles results in highly crystalline phases. The nano-particulate mixed-metal cobalt oxides were thoroughly analysed by means of X-ray diffraction, Raman spectroscopy, temperature-programmed reduction, X-ray absorption near edge structure spectroscopy, and high-resolution scanning transmission electron microscopy. This complementary characterisation of the synthesised materials allows for a distinct identification of the phases and their properties. The cobalt aluminate prepared has a cobalt-rich composition (Co<sub>1+<i>x</i></sub>Al<sub>2-<i>x</i></sub>O<sub>4</sub>) with a homogeneous atomic distribution throughout the nano-particulate structures, while the perovskite-type cobalt titanate (CoTiO<sub>3</sub>) features cobalt-lean smaller particles being associated with larger ones with an increased concentration of cobalt. The cobalt aluminate prepared showed no water-gas shift activity in the medium-shift temperature range, while the cobalt titanate sample was shown to catalyse the conversion of water and carbon monoxide to hydrogen and carbon dioxide after an extended activation period. However, this perovskite underwent vast restructuring forming metallic cobalt, a known catalyst for the water-gas shift reaction at temperatures exceeding typical conditions for the cobalt-based Fischer-Tropsch synthesis, and anatase-TiO<sub>2</sub> <i>via</i> a partial reduction of the mixed-metal cobalt oxide and segregation as identified by means of post-run X-ray diffraction.


2009 ◽  
Author(s):  
Daniela Zanchet ◽  
Cristiane B. Rodella ◽  
Laura J. S. Lopes ◽  
Marco A. Logli ◽  
Valéria P. Vicentini ◽  
...  

2019 ◽  
Vol 48 (36) ◽  
pp. 13858-13868 ◽  
Author(s):  
Moritz Wolf ◽  
Stephen J. Roberts ◽  
Wijnand Marquart ◽  
Ezra J. Olivier ◽  
Niels T. J. Luchters ◽  
...  

Mixed-metal cobalt oxide, namely cobalt aluminate and titanate, were shown to be water gas shift inactive.


2010 ◽  
Vol 156 (1-2) ◽  
pp. 2-7 ◽  
Author(s):  
Shanthakumar Sithambaram ◽  
Wen Wen ◽  
Eric Njagi ◽  
Xiong-Fei Shen ◽  
Jonathan C. Hanson ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-6 ◽  
Author(s):  
R. Bouarab ◽  
S. Bennici ◽  
C. Mirodatos ◽  
A. Auroux

Unsupported and supported iron oxide catalysts were prepared by incipient wetness impregnation method and studied in the water-gas shift reaction (WGSR) in the temperature range 350–450°C. The techniques of characterization employed were BET, X-ray diffraction, acid-base measurements by microcalorimetry and in situ diffuse reflectance infrared Fourier transform spectroscopy. MgO, TiO2, or SiO2 was added in order to (i) obtain a catalyst exempt of chromium oxide and (ii) study the effect of their acid-base properties on catalytic activity of Fe2O3. X-ray diffraction studies, and calorimetric and diffuse reflectance infrared Fourier transform measurements reveal a complete change in the physicochemical properties of the iron oxide catalyst after MgO addition due to the formation of the spinel oxide phase. These results could indicate that the MgFe2O4 phase stabilizes the reduced iron phase, preventing its sintering under realistic WGSR conditions (high H2O partial pressures).


2017 ◽  
Vol 546 ◽  
pp. 103-110 ◽  
Author(s):  
James Paterson ◽  
Mark Peacock ◽  
Ewen Ferguson ◽  
Manuel Ojeda ◽  
Jay Clarkson

2009 ◽  
Vol 145 (3-4) ◽  
pp. 188-194 ◽  
Author(s):  
José A. Rodriguez ◽  
Jonathan C. Hanson ◽  
Wen Wen ◽  
Xianqin Wang ◽  
Joaquín L. Brito ◽  
...  

2021 ◽  
Author(s):  
Zohreh Razmara

Abstract A 2D heterometallic copper(II)–sodium(I) complex based on pyridine 2,6-dicarboxylato (dipic2-) formulated as [Cu(μ-dipic)2{Na2(µ-H2O)4}]n. 2nH2O (1) has been synthesized. Thermal stability of complex 1 was studied by thermo gravimetric analysis (TGA) and differential thermal analysis (DTA). Single-crystal X-ray diffraction (SC-XRD) analysis showed that the parallelepiped colorless crystal of complex 1 crystallizes in a monoclinic system with the space group P2/c . A highly dispersed truncated octahedral catalyst formulated as Cu-Na/Al2O3 (CNM) was prepared by thermal decomposition of complex 1. Besides, the reference catalyst of Cu-Na/Al2O3 (CNR) was prepared by impregnation conventional method. The catalysts were examined by FT-IR, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer–Emmett–Teller (BET) surface area, and subjected to water-gas shift (WGS) reaction in the temperature range of 150-400 °C. The catalysts showed strong surface structure-activity dependence in WGS reaction. Improved catalytic performance during the water-gas shift reaction was observed for CNM compared to CNR due to its high dispersion, smaller particle size, and higher BET specific surface area.


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