Photocatalytic Degradation of Acid Orange 7 by NiO-TiO₂/TiO₂ Bilayer Film Photo-Chargeable Catalysts

Photocatalysis as an eco-friendly technology has the potential to achieve the Sustainable Development Goals (SDGs). However, an improvement of conventional photocatalysts is necessary to overcome their limitations such as slow kinetics, wavelength for excitation, and environmental restrictions. In particular, the development of a photocatalyst that can operate even in the absence of light is constantly conducted, and a photo-chargeable photocatalyst could be one of the answers. In this paper, a heterojunction composed of TiO2 and NiO-TiO2 bilayer film photocatalyst (BLF) was prepared. The effect of the synthesis conditions of the NiO-TiO2 layer on the photocatalytic properties was investigated. Photocatalytic degradation measurements were conducted with an acid orange 7 (AO7) solution under light and dark conditions. The highest degradation BLF was synthesized at a NiO loading of 52% and calcination temperature of 300 °C. The prepared sample showed about five-fold greater photocatalytic activity of 48% in AO7 degradation after 8 h compared to an ordinary TiO2 film (9%) under light conditions. Moreover, under dark conditions it exhibited 13.6% degradation, while the naked layers of TiO2 and NiO-TiO2 showed no degradation. The proposed mechanism suggested that photocatalysis in the dark was possible due to the stabilization of photogenerated holes by anionic intercalation during illumination

Investigation on the roles of activated carbon particle sizes on methane hydrate formation and dissociation

Chemical Engineering Science126383-38

Comparative Study of Tetra-N-Butyl Ammonium Bromide and Cyclopentane on the Methane Hydrate Formation and Dissociation

Two widely investigated methane hydrate promoters, tetra-n-butyl ammonium bromide (TBAB) and cyclopentane (CP), for methane hydrate formation and dissociation were comparatively investigated in the quiescent reactor at 2.5 °C and 8 MPa. The results indicated that the increase in the mass fraction TBAB decreased the induction time. However, it did not significantly affect the methane uptake. In the presence of CP, the increase in the CP concentration resulted in an increase in the induction time due to the increasing thicknesses of the CP layer in the unstirred reactor. Moreover, the methane uptake was varied proportionally with the CP concentration. The addition of TBAB resulted in a higher methane uptake than that of CP, since the presence of TBAB provided the cavities in the hydrate structure to accommodate the methane gas during the hydrate formation better than that of CP. On the contrary, the presence of CP significantly increased the induction time. Although the methane recovery remained relatively the same regardless of TBAB and CP concentrations, the recovery was higher in the presence of TBAB

A Revisit to the Hydrogen Desorption/Absorption Behaviors of LiAlH4/LiBH4: Effects of Catalysts

The hydrogen desorption/absorption behaviors of LiAlH4/LiBH4 with a focus on the effects of catalysts, namely TiCl3, TiO2, VCl3, and ZrCl4, were investigated using a thermal-volumetric apparatus. The hydrogen desorption was performed from room temperature to 300 °C with a heating rate of 2 °C min−1. The LiAlH4–LiBH4 mixture with a molar ratio of 2:1 decomposed between 100 and 220 °C, and the hydrogen desorption capacity reached up to 6.6 wt %. Doping 1 mol % of a catalyst to the mixture resulted in the two-step decomposition and a decrease in the hydrogen desorption temperature. All the doped samples provided lower amountz of desorbed hydrogen than that obtained from the undoped one. No hydrogen absorption was observed under 8.5 MPa of hydrogen pressure and 300 °C for 6 h. Despite the fact each of the catalysts may affect the hydrogen storage behaviors of the mixture differently, none resulted in a change in the sample reversibility

Morphology of methane hydrate formation in porous media

10.1021/ef4004818Energy and Fuels2763364-3372ENFU