Synthesized Hollow TiO<Subscript>2</Subscript>@g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> Composites for Carbon dioxide Reduction Under Visible Light

The hollow TiO₂@g-C₃N₄ composites were synthesized by a facile stirring method. The phase compositions, optical properties, and morphologies of the samples were characterized via X-ray diffraction, scanning electron microscope, transmission electron microscopy, high resolution transmission electron microscopy, fourier transform infrared spectroscopy, N₂ adsorption–desorption, UV–Vis diffuse reflectance spectroscopy and Photoluminescence. The photocatalyitc performance was evaluated by reduction carbon dioxide under visible light irradiation. The results indicated that TiO₂@g-C₃N₄ nanocomposites displayed higher photocatalytic activity compared with pure g-C₃N₄. The increased photocatalytic activity of TiO₂@g-C₃N₄ nanocomposites can be attributed to facilitating the photo-induced electron–hole separation efficiency and enhancing the photo-induced electron migration.

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Preparation of powdered carbon nitride C<Subscript>3</Subscript>N<Subscript>4</Subscript>

The basic principles of the preparation of powdered carbon nitride C₃N₄ in bulk amounts are developed. Synthetic carbon nitride C₃N₄ was identified using X-ray powder diffraction, infrared absorption, and reduction melting in a carrier gas (helium) flow with subsequent chromatographic separation.Original Russian Text Copyright © 2004 by Fizika i Khimiya Stekla, Mohammad Arif, Blinov, Lappalainen, Filippov.     

Heat treatment of silica-fiber-reinforced BN-Si<Subscript>3</Subscript>N<Subscript>4</Subscript> matrix composite

A new wave-transparent composite reinforced by silica fibers with a hybrid matrix comprising BN and Si₃N₄ was prepared by precursor infiltration and pyrolysis, and it was heat-treated at elevated temperatures. The variations of the composite during heat treatments were characterized and investigated by Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and scanning electron microscopy (SEM). The as-received composite exhibits good mechanical properties, and it is almost amorphous. When treated at 1600°C, it turned brittle, and silica fibers in it were fused; the composite showed a good crystalline form. When treated at 2100°C, the composite broke into pieces, and the composition showed only BN. Si₃N₄ was decomposed, and silica fibers were volatilized. The presence of BN probably affected the phase transitions of silica fibers. __________ Translated from Novye Ogneupory, No. 8, pp. 49–52, August 2007.     

Embedding Noble-Metal-Free Ni<Subscript>2</Subscript>P Cocatalyst on g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> for Enhanced Photocatalytic H<Subscript>2</Subscript> Evolution in Water Under Visible Light

Photocatalytic hydrogen evolution is considered as one of the promising pathways to settle the energy crises and environmental issues by utilizing solar energy. In this paper, noble-metal-free Ni₂P was used as cocatalyst to enhance g-C₃N₄ for photocatalytic hydrogen production under visible light irradiation (λ?>?420 nm). Characterization results indicated that Ni₂P nanoparticles were successfully loaded onto g-C₃N₄, which can significantly contribute to accelerate the separation and transfer of photogenerated electron. The hydrogen evolution rate reached ～?270 µmol h^?1 g^?1 and the apparent quantum yield (AQY) was ～?2.85% at 420 nm. Meanwhile, there is no obviously decrease of the hydrogen production rate even after 36 h under visible light illumination. In addition, the mechanism of photocatalytic hydrogen evolution was also elaborated in detail.

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Polyaniline/g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> composites as novel media for anticorrosion coatings

In this paper, graphitic carbon nitride (g-C₃N₄) was first proposed for the pioneer application of anticorrosion coatings. Original g-C₃N₄ was facilely treated using HNO₃ and the exfoliated g-C₃N₄ sheets (E-g-C₃N₄) were fabricated, and then, polyaniline/E-g-C₃N₄ composites (PANI/E-g-C₃N₄) as novel anticorrosive media were synthesized by chemical oxidative polymerization and devoted to the corrosion protection of coatings. The E-g-C₃N₄ sheets and PANI/E-g-C₃N₄ composites were characterized by X-ray diffraction, Fourier transform infrared, thermogravimetric analysis, and transmission electron microscopy. The anticorrosion properties of the samples prepared were investigated by electrochemical measurements including Tafel plots, electrochemical impedance spectra, and open-circuit potential. Accelerated corrosion tests of iron panels coated by PANI/E-g-C₃N₄ were performed in 3.5 wt% NaCl solution. Anticorrosive mechanism of PANI/E-g-C₃N₄ was discussed in detail. PANI/E-g-C₃N₄-3 fillers possessed superior corrosion inhibition than individual components on iron coatings, which was due to the synergetic effect of anticorrosion between E-g-C₃N₄ and PANI.     

Adsorption characteristics analysis of CO<Subscript>2</Subscript> and N<Subscript>2</Subscript> in 13X zeolites by molecular simulation and N<Subscript>2</Subscript> adsorption experiment

The adsorption characteristics of CO₂ and N₂ in 13X zeolites have been studied by the molecular simulation and N₂ adsorption experiment. It is found that the simulation results by Dreiding force fields are in an agreement with the published data. The influence of the σ and ε parameters of O_Z and Na⁺ on the adsorption performance is discussed. Then the optimized force field parameters are obtained. Specific surface area (S _B ) is calculated by simulation and experiment. Its relative error is just only 4.3 %. Therefore, it is feasible that S _B of 13X zeolites is obtained by the simulation methods. Finally, the impacts of pressure and temperature on adsorption characteristics are investigated. At low pressure, CO₂ adsorption in 13X zeolites belongs to the surface adsorption. As the pressure increase, the partial multilayer adsorption appears along with the surface adsorption. N₂ adsorption in 13X zeolites is different from that of CO₂. At low temperature of 77 K, two primary peaks are caused by the surface adsorption and multilayer adsorption respectively regardless of pressure variation. When the temperature is 273 K, the energy distribution curve appears undulate at low pressures. Then it becomes stable with the pressure increase. The surface adsorption plays an important role at the relative high pressures. The results will help to provide the theory guide for the optimization of force field parameters of adsorbents, and it is very important significance to understand the adsorption performance of zeolites.     

Synthesis of MIL-101@g-C<Subscript>3</Subscript>N<Subscript>4</Subscript> nanocomposite for enhanced adsorption capacity towards CO<Subscript>2</Subscript>

MIL-101@g-C₃N₄ nanocomposite was prepared by solvothermal synthesis and used for CO₂ adsorption. The parent materials (MIL-101 and g-C₃N₄) and the MIL-101@g-C₃N₄ were characterized by X-ray diffraction, argon adsorption/desorption, Fourier transform infrared spectroscopy, thermal analysis (TG/DTA), transmission electronic microscopy, and Energy-dispersive X-ray spectroscopy. The results confirmed the formation of well-defined MIL-101@g-C₃N₄ with interesting surface area and pore volume. Furthermore, both MIL-101 and MIL-101@g-C₃N₄ were accomplished in carbon dioxide capture at different temperatures (280, 288, 273 and 298 K) at lower pressure. The adsorption isotherms show that the nanocomposite has a good CO₂ adsorption affinity compared to MIL-101. The best adsorption capacity is about 1.6 mmol g^?1 obtained for the nanocomposite material which is two times higher than that of MIL-101, indicating strong interactions between CO₂ and MIL-101@g-C₃N₄. This difference in efficacy is mainly due to the presence of the amine groups dispersed in the nanocomposite. Finally, we have developed a simple route for the preparation of an effective and new adsorbent for the removal of CO₂, which can be used as an excellent candidate for gas storage, catalysis, and adsorption.     

Dry Sliding Friction and Wear Behavior of AA7075-Si<Subscript>3</Subscript>N<Subscript>4</Subscript> Composite

The present investigation is aimed at identifying the influence of Si₃N₄ reinforcement on the mechanical and tribological behavior of AA7075-Si₃N₄ composite. Five different composites of AA7075 aluminum alloy reinforced by silicon nitride particles have been fabricated by the stir casting route. The percentage of silicon nitride was varied from 0-8 wt%. The cast composites were tested for hardness, density and compression strength. Unidirectional friction and wear testing was carried out for all compositions under five different loading conditions (10 N, 20 N, 30 N, 40 N and 50 N) at a constant sliding speed of 1 m/s. SEM and EDS analysis was also carried out for worn surface analysis and elemental analysis of the composites. The hardness and compression strength of the composites exhibited an increasing trend with an increase in wt% of reinforcement in the base alloy, showing 20% improvement in hardness and around 50% improvement in compression strength for 8 wt% Si₃N₄ addition. The addition of Si₃N₄ particles led to an improvement in the wear resistance by 37% at low loads (10 N) and 61% at higher loads (50 N). The COF for all varied compositions at low load (10 N) and high load (50 N) ranges from 0.10 to 0.20 and 0.25 to 0.30 respectively. Moreover, the COF is observed to increase until 4 wt% and beyond it decreases. Microscopic studies of worn surfaces revealed a dominance of delamination wear at lower concentrations (0 wt% and 2 wt%) and ploughing at higher concentrations (6 wt% and 8 wt%). The developed composites exhibited better mechanical and anti-wear properties and could serve as potential candidates in sliding applications such as bearings, brake drums, gears, sprockets and brake rotors.     

Recyclable Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>@Tween20@Ag Nanocatalyst for Catalytic Degradation of Azo Dyes

Silver nanoparticles supported on superparamagnetic iron oxide (SPION)-Tween20 nanocomposite were prepared by a combined polyol and chemical reduction routes. The morphology, composition and structure of Fe₃O₄@Tween20@Ag nanocatalyst were characterized by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy, energy dispersive X-ray spectroscopy, thermal gravimetric analyzer, and X-ray powder diffraction. In addition the magnetic properties were evaluated with vibrating sample magnetometry. It was found that Fe₃O₄@Tween20@Ag nanocatalyst could catalyze the degradation of various organic azo dyes and could easily be recovered from the reaction medium with external magnet. Also, the magnetic catalyst can be succesfully recycled and reused for at least five successive degradation cycles of methyl orange, methylene blue and Rhodamine B, confirming a high recycling efficiency. The cost effective and recyclable Fe₃O₄@Tween20@Ag nanocatalyst provide an novel nanomaterials architecture for environmental remediation applications.     

Thermophysical properties of composite materials in the Si<Subscript>3</Subscript>N<Subscript>4</Subscript> - BN system

The results of a study of the thermophysical properties (thermal diffusivity, heat capacity, heat conductivity, and coefficient of linear thermal expansion) of Si₃N₄ - BN hot-pressed composite (with BN concentration varying from 10 to 60 wt.%) in the temperature range of 20 – 900°C are reported.__________Translated from Novye Ogneupory, No. 10, pp. 47 – 49, October, 2004.     

Selective oxidation of hydrogen sulfide over LaCoO<Subscript>3</Subscript> and LaSrCoO<Subscript>4</Subscript> mixed oxides

Perovskite LaCoO₃ and perovskite-like LaSrCoO₄ mixed oxides were prepared by polyglycol gel method, and their catalytic performance was compared for the selective oxidation of hydrogen sulfide in a stream containing excess amount of ammonia and water for the first time. These samples were investigated by using XRD, BET, O₂-TPD and XPS. The catalytic activity and the selectivity to solid products (ammonium thiosulfate and elemental sulfur) of LaCoO₃ were better than those of LaSrCoO₄, and this is explained in terms surface contents of oxygen and cobalt, oxidation state of cobalt, and BET surface area.     

High Performance Removal of Anionic and Cationic Dye Pollutants with Co<Subscript>3</Subscript>O<Subscript>4</Subscript> Modified Nanoclinoptilolite: Kinetics and Adsorption Equilibrium Studies

In this paper Co₃O₄ doped nanoclinoptilolite was synthesized and characterized by X-ray diffraction (XRD), Fourier transform infrared (FTIR), field emission scanning electron microscopy (FESEM) and energy-dispersive X-ray spectroscopy (EDX) techniques. The adsorption efficiency for removing of methylene blue was about 95% in 10 min. The effect of some factors such as adsorbent dose, concentration of analyte and pH was investigated for enhancing the removing efficiency. Moreover Freundlich and Langmuir patterns were plotted for this new nanocomposite. Maximum of adsorption capacity was obtained from slope of Langmuir and was about 25 mg/g. The kinetic study for methylene blue shows a second order kinetic with rate constant about 0.02 g/mg/min. The prepared nanocomposite was successfully applied for removing some color compounds such as methylene blue, methyl green, and methyl red and also binary dye mixtures.     

Selective Synthesis of Fe<Subscript>2</Subscript>O<Subscript>3</Subscript> and Fe<Subscript>3</Subscript>O<Subscript>4</Subscript> Nanowires Via a Single Precursor: A General Method for Metal Oxide Nanowires

Hematite (α-Fe₂O₃) and magnetite (Fe₃O₄) nanowires with the diameter of about 100 nm and the length of tens of micrometers have been selectively synthesized by a microemulsion-based method in combination of the calcinations under different atmosphere. The effects of the precursors, annealing temperature, and atmosphere on the morphology and the structure of the products have been investigated. Moreover, Co₃O₄ nanowires have been fabricated to confirm the versatility of the method for metal oxide nanowires.