Decontamination of 2-chloroethyl ethylsulfide using titanate nanoscrolls

Protonated Titanates and TiO2 Nanostructured Materials: Synthesis, Properties, and Applications

“…[90] Most of the catalytic studies are focused on the use of this mesoporous semiconductor as a high-surface-area catalyst support. There are several examples of TiO 2 nanotubes as mesoporous catalyst supports for different nanoparticles: CdS decorated TiO 2 nanotubes [91,92] and Zn 2+ doped nanotubes [93] in the reaction of photocatalytic oxidation of dyes, Pd-TiO 2 nanotube catalysts [94] for anodic oxidation of methanol, Pt-TiO 2 nanotube photocatalysts for generation of H 2 , [95] Au-TiO 2 nanotube catalyst for the water-gas shift reaction [96] and CO oxidation, [97] RuO 2 -TiO 2 nanotubes as an electrocatalyst for reduction of CO 2 , [86] and ruthenium(III) hydrated oxide deposited on TiO 2 nanotubes for selective oxidation of alcohols [78] ( Table 5).…”

Deposition of Pt, Pd, Ru and Au on the surfaces of titanate nanotubes

“…The relatively low cost of the titanate nanotubes compared to the TiO 2 nanotubes produced by sol-gel template assisted methods, renders the present materials attractive for technological applications. Although titanate nanotubes demonstrate moderate catalytic activity as acid base catalysts [16,23] there are few demonstrated examples of the successful utilisation of titanate nanotubes as mesoporous catalyst supports for different nanoparticles: CdS decorated titanate nanotubes [24,25] in reaction of photocatalytic oxidation of dyes, Pd/TiO 2 nanotubes catalyst [26] for electro-oxidation of methanol, Pt/TiO 2 nanotubes photocatalyst for generation of H 2 [14], Au/TiO 2 nanotubes catalyst for water-gas shift reaction [27], RuO 2 /TiO 2 nanotubes electro-catalyst for reduction of CO 2 [22] and ruthenium (III) hydrated oxide deposited on titanate nanotubes for selective oxidation of alcohols [28].…”

Key role of terminal hydroxyl groups and visible light in the reactive adsorption/catalytic conversion of mustard gas surrogate on zinc (hydr)oxides

“…It has been reported that once EES + is formed, it may be converted to a cyclic cation through an intermolecular cyclization process [33,[43][44][45][46]. After that, a labile hydrogen from the cation transfers to the negative charged lattice oxygen of the zinc phase, that acts like a Lewis base [47,48].…”