On Structural,Optical, and Electrical Properties of Chromium Oxide Cr2O3 Thin Film for Applications

Protection of Metals and Physical Chemistry of Surfaces - Chromium oxide thin films were grown on Al2O3 substrates by ablating a pure Cr2O3 target using a KrF excimer laser. The energy density on...     

Determination of trace amount of silver in water samples by flame atomic absorption after preconcentration by ZnO nano sorbent

A simple and fast method based on solid phase extraction (SPE) applying zinc oxide (ZnO) nanoparticles and atomic absorption spectrometry (AAS) was developed for the trace amount determination of silver (Ag) in aqueous samples. The method linearity was in the range of 14 to 700 ng mL^?1. The extraction efficiency of Ag was greater than 98% and limit of detection (LOD) was 4.2 ng mL^?1. The preconcentration factor was 200 and the relative standard deviation (RSD%) of the method was 3.7% (n = 6).     

Pseudo stir bar sorptive microextraction fiber using nanoparticles reinforcedsol–gel for the determination of Co(II) and Cd(II) ions in wastewaters

In this work a newly semi polar extraction phase of carboxylated multiwalled carbon nanotube (MWCNTs) reinforced sol-gel immobilized polypropylene hollow fiber was prepared by low temperature hydrothermal process. It is coupled with flame atomic absorption spectroscopy was employed in the extraction and determination of cobalt and cadmium ions in wastewaters. The main factors influencing the pre-concentration and extraction of the metal ions have been examined in detail. Detection limits obtained in this way for Co(II) and Cd(II) ions were 0.0186 and 0.024 ng mL^?1, respectively.     

Magnetic solid phase extraction of copper from aquatic samples by Fe3O4/SiO2 nanoparticles followed by atomic absorption spectrometric determination

A magnetic solid phase extraction was developed for preconcentration of Cu(II) as a 4-bromo-2-(2,4-dichloro-phenylimino)-phenol complex on Fe₃O₄/SiO₂ nanoparticles prior to its determination by atomic absorption spectroscopy. The effect of different parameters influencing the formation of the Cu complex and the extraction efficiency of the Cu complex were studied. Under optimal conditions, the calibration graph showed linearity in the range of 0.946–700 µg L^?1 (R² = 0.9995) of Cu(II). The limit of detection and relative standard deviation of the method (n = 6) were 0.283 µg L^?1 and 3.0%, respectively. The method was successfully applied to determine copper (II) in water samples.     

MnO2 Nanoparticles as Efficient Oxidant for Ultrasound-Assisted Synthesis of 2-substituted Benzimidazoles under Mild Conditions

In this article, a novel method for synthesis of 2-substituted benzimidazoles using MnO₂ nanoparticles as a convenient oxidant agent in ethanol-water (1:1) as solvent under ultrasound irradiation was demonstrated. In this protocol the desired products were purely obtained in high yields. The main advantages of this research are: mild procedure, simplicity of method, easily work-up, high yields, and short reaction times. The MnO₂ nanoparticles were synthesized through a solid-state reaction route using simple strarting materials. Furthermore, their structure was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FT-IR).     

Synthesis and characterization of diethyl-dithiocarbamic acid 2-[4-(2-diethylthiocarbamoylsulfanyl-2-phenyl-acetyl)-2,5-dioxo-piperazin-1-yl]-2-oxo-1-phenyl-ethyl ester as new reversible addition-fragmentation chain transfer agent for polymerization of ethyl methacrylate

Diethyl-dithiocarbamic acid 2-[4-(2-diethylthiocarbamoylsulfanyl-2-phenyl-acetyl)-2,5-dioxo-piperazin-1-yl]-2-oxo-1-phenyl-ethyl ester as a novel di-functional reversible addition–fragmentation chain transfer (RAFT) agent was synthesized based on 2,5-diketopiperazine. The RAFT agent was designed based on the propagating core (R group) approach and characterized by ¹H NMR, ¹³C NMR, FT-IR, elemental analysis, and melting point technique. Then, ethyl methacrylate was synthesized via free radical and RAFT polymerizations. To investigate the effect of the RAFT agent on the kinetic of polymerization, molecular weight, and polydispersity index (PDI) of polymers and also monomer conversion were monitored. Also, synthesized polymers were characterized by ¹H NMR, ¹³C NMR, FT-IR, and TGA. Characterization analyses of synthesized RAFT agent were consistent with the structure. NMR and FTIR analyses confirmed end group incorporation of RAFT agent into polymer structure. According to results, poly(ethyl methacrylate) with low PDI (1.14) was obtained. Kinetic study indicated well-controlled polymerization of ethyl methacrylate by synthesized RAFT agent. TGA results showed that RAFT agent could reduce termination reactions and so reduce head-to-head bonds and chain-end unsaturation by keeping the concentration of radicals low enough.     

Room Sharing in Sydney: A Complex Mix of Affordability,Overcrowding and Profit Maximisation

The shared housing sector is a growing private rental submarket. Researchers have sought to analyse the drivers of this growth, the benefits of shared housing for tenants, landlords and wider urban systems, as well as risks for tenants and local planning systems. Yet, there is limited research exploring the diversity of the shared housing sector. In particular, analysis of room or space sharing with non-related adults is lacking. This paper explores the characteristics, geography and impact of room sharing across Sydney. By analysing online accommodation listings this paper provides insights for policymakers seeking to monitor and regulate shared room accommodation.     

Synthesis,Thermal Properties and Electrical Conductivity of Na-Sialate Geopolymer

This work aims to study the thermal behavior of basic-geopolymers derived from metakaolin (clay). The geopolymers were characterized by different techniques: thermal analysis (DTA, TGA), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and impedance spectroscopy. Some physicochemical properties of the products were also determined: the phases obtained after geopolymer heat treatment and their electrical properties. The results obtained after drying and heat treatment showed that the products kept their initial shapes, but revealed variable colors depending on the temperatures at which they were treated. The products obtained are amorphous between 300 up to 600 °C with peaks relating to the presence of nanocrystallites of muscovites and zeolite, thus at 900 °C it is quite amorphous but only contains nanocrystallites of muscovites. From the temperature of 950 °C, we notice that the geopolymer has been transformed into a crystalline compound predominated by the Nepheline (NaAlSiO₄) with the presence of a crystalline phase by minor peaks of Muscovite, this crystalline character has been increased at 1100 °C to obtain a whole phase crystalline of a Nepheline. The treatment of this geopolymer for one hour at 1200 °C shows an amorphous phase again corresponding to corundum (α-Al₂O₃). This indicates that the dissolution of the grains by the liquid phase induces the conversion of the material structure from sialate [–Si–O–Al–O] to sialate siloxo [–Si–O–Al–O–Si–O–] and the formation of a new crystalline phase (α-Al₂O₃). This development of sialate to sialate-siloxo was confirmed by IR spectroscopy. As mentioned above, from 300 to 900 °C, Na-sialate geopolymer exhibits the same disorder structure of nepheline. The crystal structure of nepheline is characterized by layers of six-membered tetrahedral rings of exclusively oval conformation. The rings are built by Regularly alternating tetrahedral AlO₄ and SiO₄. Stacking the layer’s parallel to the c axis gives a three-dimensional network containing channels occupied by Na cations. This topology favors easy movement of Na⁺ ions throughout the structure. For this reason, ionic migration in nepheline is widely reported. The refinement of Na-Sialate geopolymer at room temperature gives bulk high ionic conductivity of about 5 × 10^?5 S cm^?1 and this is due to the probable joint contribution of H⁺ and Na⁺ ions. Above 200 °C, Na⁺ seems to remain the only charge carrier with a low activation energy of about Ea?=?0.26 eV. At higher temperatures, the characteristic frequencies become so close that it is impossible to distinguish the contributions. A total resistance comprising both grain and grain boundaries contribution is then determined.

     

The effect of substrate surface integrity on the surface properties of TiCrN coating applied via the CAE-PVD method

This study aims to investigate how the predeposition machining processes such as magnetic grinding, turning machining, and wire electrical discharge machining can influence the surface properties including electrochemical and tribological behavior of TiCrN nanostructured coating applied on Mo40 steel substrate. A physical vapor deposition technique using cathodic arc evaporation was used to apply the coating. The crystallographic phases and the microstructure of the coating were studied by X-ray diffraction and scanning electron microscope, respectively. Rockwell-C, electrochemical impedance spectroscopy and potentiodynamic polarization, and pin-on-disk wear tests were employed to evaluate the adhesion strength, corrosion behavior, and tribological property of specimens, respectively. The electrochemical results after 24 h of exposure to 3.5 wt% NaCl solution showed that TiCrN coating pretreated with a turning process with polarization resistance of about 3525.32 Ω.cm² had the best corrosion resistance among all specimens. This was because of the improvement of the smoothness, surface quality, and adhesion after the turning process. On the other, the friction coefficient of the grounded sample is less than that of other ones. This is probably due to its higher adhesion strength and higher surface smoothness.     

Thermal Stability Investigation of Synthesized Epoxy-Polyurethane/Silica Nanocomposites

Silicon - In this research, epoxy polyurethane-nano silica nanocomposites have been synthesized using an in-situ method, for which SiO2 nanocomposites had been initially ready in N,...