Gas Sensing Properties of Cobalt Titanate with Multiscale Pore Structure: Experiment and Simulation

A diffusion-reaction coupled model was presented to investigate the effects of multiscale pore structure characteristics on gas sensing properties. A series of CoTiO3 powders with different pore size distributions were fabricated by sol-gel method. Experimental results on cobalt titanate thick films show that a well-defined multiscale pore structure is particularly desired for the improvement of sensing performance, instead of just increasing the specific surface area. The theoretical responses of sensing elements with different pore size distributions were derived and compared with experimental data on CoTiO3 sensors exposed to ethanol. The calculated sensitivities considering the influence of pore size changes were also found to be in agreement with the experimental results. A dimensionless Thiele modulus Th was introduced for assessing the critical point corresponding to the transformation from surface reaction-controlled sensitivity into diffusion-controlled sensitivity.

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

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_1+<i>x</i>Al_2-<i>x</i>O₄) with a homogeneous atomic distribution throughout the nano-particulate structures, while the perovskite-type cobalt titanate (CoTiO₃) 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-TiO₂ <i>via</i> a partial reduction of the mixed-metal cobalt oxide and segregation as identified by means of post-run X-ray diffraction.

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

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_1+<i>x</i>Al_2-<i>x</i>O₄) with a homogeneous atomic distribution throughout the nano-particulate structures, while the perovskite-type cobalt titanate (CoTiO₃) 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-TiO₂ <i>via</i> a partial reduction of the mixed-metal cobalt oxide and segregation as identified by means of post-run X-ray diffraction.