Nanostructured Layers for Catalytic ApplicationsView this Special Issue
Nanostructured Layers for Catalytic Applications
Higher energy consumption, which is a result of increasing the world population, gives rise to decreasing in fossil fuel reserves and creating environmental pollutions. Pollution is the introduction of contaminants into a natural environment that causes instability, disorder, harm, or discomfort to the ecosystem and can take the form of chemical substances or energy, such as noise, heat, or light. Remediation of the environmental pollutants is necessary. Since now three decades, advanced oxidation technologies “in particular photocatalysis” gained much attention by scientifics. In their point of view, to counter environmental pollutions, a simple and comprehensive photonic reaction system which converts the solar energy into the chemical energy of a redox system, namely, photocatalysis, would be helpful for the detoxification processes. Nowadays, heterogeneous photocatalysis is the most efficient method for destroying organic pollutants in especially aqueous media. This process is based on the use of ultraviolet or visible radiations to excite a semiconductor on whose surface the oxidation of the pollutants is performed. This special issue addresses advances in nanostructured layers for photocatalytic applications.
In the first paper of this special issue, ZnO nanoparticles were deposited on Si, Si/Au, and Si/Au/ZnO substrates by mist atomization, and effect of the substrates conditions on the structural, morphological, and photoluminescence properties of the nanoparticles was investigated. It was found that crystallite size and lattice strain were significantly affected by substrate surface type and temperature. Smallest crystallite size was obtained on Si/Au/ZnO at 400°C. The second paper deals with effect of Ti3+ on photocatalytic efficiency of titanium dioxide. The authors revealed that physical and chemical properties of TiO2 were dominantly determined by its surface condition and especially presence of Ti3+ species on its surface. A formation mechanism for the aforementioned defect was also proposed in this paper. Various generation methods for Ti3+ surface defect as well as its effect on optical and photocatalytic properties were discussed. It was shown that a detailed picture of Ti3+ surface defects would help to understand reactivity and overall material performance in photocatalytic applications. Ag-Cu bimetallic catalysts were prepared by microemulsion method, and their catalytic performance in epoxidation of styrene was evaluated in the third paper of this special issue. In this study, deposition of Ag-Cu bimetallic nanoparticles by the coreduction of Ag+ and Cu2+ cations with N2H4·H2O as reductant on reticulate-like γ-alumina particles was studied. Ag-Cu bimetallic nanoparticles supported by γ-alumina showed better catalytic activity on the epoxidation of styrene as compared with the corresponding monometallic silver or copper catalysts. Herein, these could also be promising candidates for applications in many other reactions, namely, CO oxidation. In the next paper, porous diatomite immobilized Cu-Ni bimetallic nanocatalysts for direct synthesis of dimethyl carbonate. Upon various characterizations, it was shown that the bimetallic composite is effectively alloyed and well immobilized inside or outside the structural pores. In addition, the authors showed that existence of electron-rich and electron-deficient centers is resulted from the strong interaction of diatomite with Cu-Ni, and the synergy of Cu-Ni alloy may be responsible for the high performance of this catalyst. Fabrication of photofunctional nanoporous alumina membrane (PNAM) and its photoinactivation effect of vesicular stomatitis virus were reported in the fifth paper. To open the possibility for its environmental application, PNAM was applied for the removal of a virus without rendering cytotoxicity to the cells in vitro. The authors concluded with the complete suppression of plaque-forming ability of vesicular stomatitis virus (VSV) by PNAM-mediated PACT (photodynamic antimicrobial chemotherapy). In the next paper entitled “the physical properties of erbium-doped yttrium iron garnet films prepared by sol-gel method” thin films of were deposited through sol-gel method. These crystalline films were found to be soft magnetic materials. The saturation magnetization is reduced with Er substitution because the magnetic moments of Er3+ ions coupled antiferromagnetically to the effective moment formed by Fe3+ ions. The maximum coercivity was obtained at . In the next paper, a decrease in NiO-MgO phase through its solid solution equilibrium with tetragonal and its effect on catalytic partial oxidation of methane were investigated. The main concept of this study is utilizing the solid-state reaction equilibrium between the two solid solutions: the rock salt NiO-MgO and the tetragonal (LSNM) phase in order to reduce the size of NiO-MgO. This size reduction aimed to improve the coke resistance of the Ni0 catalyst in the partial oxidation of methane (POM) without compromising the activity of catalyst. In the eighth paper, catalytic activity of ZrO2 nanotube arrays prepared by anodizing method was studied, where nanotubes were prepared in aqueous electrolyte containing (NH4)2SO4 and NH4F. Calcination temperature and electrolyte concentration have a great influence on catalytic activity. Results indicate that nanotube arrays have highest catalytic activity when the concentration of (NH4)2SO4 is 1 mol/L, the concentration of NH4F is 1 wt%, and the calcination temperature is 400°C. Finally, modification of clays by sol-gel reaction and their use in the ethylene in situ polymerization for obtaining nanocomposites was reported. It was given away that the catalytic activity significantly increases when the clays were modified via sol-gel reaction under acidic or basic conditions compared with neutral condition.
M. R. Bayati
H. R. Zargar