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See detailStudy of the photocatalytic activity of Fe3+, Cr3+, La3+ and Eu3+ single-doped and co-doped TiO2 catalysts produced by aqueous sol-gel processing
Malengreaux, Charline; Pirard, Sophie ULg; Léonard, Géraldine ULg et al

in Journal of Alloys and Compounds (2017), 691

An aqueous sol-gel process, previously developed for producing undoped and Cu2+, Ni2+, Zn2+ or Pb2+ doped TiO2 photocatalysts with remarkably high photocatalytic activity without requiring any calcination ... [more ▼]

An aqueous sol-gel process, previously developed for producing undoped and Cu2+, Ni2+, Zn2+ or Pb2+ doped TiO2 photocatalysts with remarkably high photocatalytic activity without requiring any calcination step, has been adapted to produce Fe3+, Cr3+, La3+ or Eu3+ single-doped TiO2 photocatalysts as well as La3+-Fe3+ and Eu3+-Fe3+ co-doped TiO2 catalysts. The physicochemical properties of the obtained catalysts have been characterized using a suite of complementary techniques, including ICP-AES, XRD, UV-Vis spectroscopy, nitrogen adsorption-desorption and Fe-57 Mössbauer. The active crystalline phase is obtained without requiring any calcination step and all the different catalysts are composed of nanocrystallites of anatase with a size of 6-7 nm and a high specific surface area varying from 181 to 298 m² g-1. In this study, the effect of the NO3:Ti(IV) mole ratio used to induce the peptisation reaction during the synthesis has been studied and the results revealed that this ratio can influence significantly the textural properties of the resulting catalyst. A screening of the photocatalytic activity of the undoped and Fe3+, Cr3+, La3+ or Eu3+ single-doped and co-doped photocatalysts has been performed by evaluating the degradation of 4-nitrophenol under UV-Visible light (330 nm < λ < 800 nm). This study suggests that the photocatalytic activity is significantly influenced by the dopant nature and content with an optimal dopant content being observed in the case of Fe3+ or La3+ single-doped as well as in the case of La3+-Fe3+ and Eu3+-Fe3+ co-doped catalysts. In the case of Cr3+ single-doped catalysts, a detrimental effect of the dopant on the photocatalytic degradation of 4-nitrophenol has been observed while no significant influence of the dopant has been detected in the case of Eu3+ single-doped catalysts. The role of the different dopants in modulating the photocatalytic activity is discussed. [less ▲]

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See detailKinetics of water pollutants degradation through the use of ions doped photocatalysts
Malengreaux, Charline; Pirard, Sophie ULg; Bartlett, John et al

Conference (2015)

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See detailAqueous sol-gel chemistry for the production of titanate-based nanopowders and gels for environmental applications
Malengreaux, Charline; Heinrichs, Benoît ULg; Bartlett, John

Conference (2014)

Detailed reference viewed: 19 (1 ULg)
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See detailKinetic study of 4-nitrophenol photocatalytic degradation over a Zn2+ doped TiO2 catalyst prepared through an environmentally friendly aqueous sol–gel process
Malengreaux, Charline ULg; Pirard, Sophie ULg; Bartlett, John et al

in Chemical Engineering Journal (2014), 245

A kinetic study of the photocatalytic degradation of 4-nitrophenol (4-NP) under UV–visible light (330 nm < k < 800 nm) has been performed via a rigorous chemical engineering approach over a Zn2+ doped ... [more ▼]

A kinetic study of the photocatalytic degradation of 4-nitrophenol (4-NP) under UV–visible light (330 nm < k < 800 nm) has been performed via a rigorous chemical engineering approach over a Zn2+ doped TiO2 catalyst prepared through an environmentally friendly aqueous sol–gel process. The experiments have been performed at three temperatures to enable the global activation energy to be estimated. The influence of the illumination intensity has also been considered. The possibility of internal and external diffusion limitations has been studied and the results obtained demonstrated that there is no diffusional limitation during the photocatalytic degradation of the 4-NP using the selected catalyst. Therefore, the apparent specific reaction rate measured corresponds to the actual reaction rate of the chemical reaction. Parameter adjustments show that the kinetic model that provides the best fit to the experimental data corresponds to a first order reaction. A sequence of elementary steps has been considered and a pseudo-steady state approach based upon the stationary state hypothesis for reaction intermediates has been applied to obtain a kinetic rate expression in agreement with the experimental data. The mean values of the reaction rate constant found at 283 K, 288 K and 293 K are respectively equal to k1 = 0.094 ± 0.003 m3 h- 1 kgcatalyst- 1; k2 = 0.119 ± 0.004 m3 h- 1 kgcatalyst- 1 and k3 = 0.150 ± 0.023 m3 h- 1 kg catalyst-1 and the global activation energy of the degradation reaction was evaluated as 40 kJ mol-1. A phenomenological kinetic mechanism is proposed to describe the reaction at a molecular scale. Finally, statistical validations and residuals analysis have been performed to confirm that the first order model is suitable to represent the 4-NP photocatalytic degradation over time. Such studies are essential to design a reactor for water pollutant degradation on an industrial scale. [less ▲]

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See detailDevelopment of Highly Active doped Titania Photocatalysts by Aqueous Sol-Gel Processing
Malengreaux, Charline ULg; Douven, Sigrid ULg; Poelman, Dirk et al

Poster (2012, December)

Detailed reference viewed: 44 (16 ULg)
See detailDevelopment of Highly Active doped Titania Photocatalysts by Aqueous Sol-Gel Processing
Malengreaux, Charline ULg; Douven, Sigrid ULg; Poelman, Dirk et al

Poster (2012, November)

Detailed reference viewed: 31 (14 ULg)