Genesis of nanocrystalline Ho2O3 via thermal decomposition of holmium acetate: Structure evolution and electrical conductivity properties

This study focuses on the preparation of nanostructured holmium oxide via the decomposition of holmium acetate precursor utilizing the non-isothermal strategy. Thermogravimetric analysis(TGA) was used to follow up the various thermal events involved in the decomposition process. Dehydration completes approximately at 150℃, which is followed by the decomposition of the anhydrous acetate leading to the formation of holmium oxide. Based on the TGA results the acetate precursor was heated non-isothermally at the temperature range of 150 e700℃. The obtained solids were characterized using powder X-ray diffraction(XRD), X-ray photoelectron spectroscopy(XPS), Fourier transform infrared spectroscopy(FT-IR), field-emission scanning electron microscopy(FE-SEM) and transmission electron microscopy(TEM). It is found that nanocrystalline Ho_2 O_3 starts to form at 500℃ and presents the only phase detected at the 500 e700℃ range. The electrical conductivity of the solids that form at the temperature range of 300 e700℃ was investigated. The obtained values were correlated with the observed structural modifications accompanying the heat treatment. The electrical conductivity of the Ho_2 O_3 samples prepared at 500, 600 and 700℃ reaches the values of 1.92 × 10~(-7), 1.61 × 10~(-7) and 8.33 × 10~(-8) Ω~(-1)cm~(-1) at a measuring temperature of 500℃, respectively. These values are potentially advantageous for high-resistivity devices.     

Review on zirconate-cerate-based electrolytes for proton-conducting solid oxide fuel cell

The performance of low-to-intermediate temperature (400–800?°C) solid oxide fuel cells (SOFCs) depends on the properties of electrolyte used. SOFC performance can be enhanced by replacing electrolyte materials from conventional oxide ion (O^2-) conductors with proton (H⁺) conductors because H⁺ conductors have higher ionic conductivity and theoretical electrical efficiency than O^2- conductors within the target temperature range. Electrolytes based on cerate and/or zirconate have been proposed as potential H⁺ conductors. Cerate-based electrolytes have the highest H⁺ conductivity, but they are chemically and thermally unstable during redox cycles, whereas zirconate-based electrolytes exhibit the opposite properties. Thus, tailoring the properties of cerate and/or zirconate electrolytes by doping with rare-earth metals has become a main concern for many researchers to further improve the ionic conductivity and stability of electrolytes. This article provides an overview on the properties of four types of cerate and/or zirconate electrolytes including cerate-based, zirconate-based, single-doped cerate–zirconate and hybrid-doped cerate–zirconate. The properties of the proton electrolytes such as ionic conductivity, chemical stability and sinterability are also systematically discussed. This review further provides a summary of the performance of SOFCs operated with cerate and/or zirconate proton conductors and the actual potential of these materials as alternative electrolytes for proton-conducting SOFC application.     

Efficient conversion of light paraffinic naphtha to aromatics over metal-modified Mo/MFI catalysts

Journal of Porous Materials - The transformation of light naphtha to value-added aromatic compounds is gaining momentum in the petrochemical industry. In this work, a series of metal modified...     

Adsorption of U(Ⅵ) from acid solution on a low-cost sorbent:equilibrium,kinetic, and thermodynamic assessments

In this paper, waste clay was cured with ethyl acetate to obtain treated clay(TC), which was modified with gallic acid to obtain a low-cost sorbent that was characterized by EDX, SEM, and FTIR analysis. Uranium(Ⅵ) adsorption was achieved using the batch adsorption method on the TC and gallic acid-modified treated clay(GMTC). The maximum uptakes of U(Ⅵ) on TC and GMTC were 37.2 and 193.0 mg/g, respectively.The U(Ⅵ) adsorption kinetics on the TC and GMTC sorbents were well-fitted by the pseudo-second-order mechanism, and the adsorption equilibrium followed the Langmuir model. The optimum parameters were applied to El Sela leach solution for uranium recovery.     

Synthesis of a novel inorganic cation exchanger based on molybdate: Applications for removal of Pb2+, Fe3+ and Mn2+ ions from polluted water

A novel manganese phosphomolybdate exchanger was synthesized, dried at different temperatures, and evaluated for the elimination of lead, iron, and manganese ions from aqueous solutions. The chemical structure of the cation exchanger was established using Fourier-transform infrared, scanning electron microscopy, Thermo gravimetric analysis/ Differential thermal analysis, and X-ray diffraction. The adsorption performance of the heavy metals Pb²⁺, Fe³⁺, and Mn²⁺ toward the synthesized material has been studied. The obtained outcomes show that the selectivity of the cationic exchanger was descending in this order, Pb²⁺ > Fe³⁺ > Mn²⁺. The highest adsorption capacity was shown to be decreased as drying temperature of the exchanger increases from 50°C to 800°C.     

Magnetron sputtered Dy_2O_3 with chromium and copper contents for antireflective thin films with enhanced absorption

Dy_2O_3 is a rare earth oxide having a number of advanced applications in various fields including protective or antireflective coatings, Main objective of this novel research work is to check the effect of Cr and Cu addition on different properties of Dy_2O_3 and achievement of antireflective thin films with enhanced abso rption. Thin films of these materials we re deposited using DC magnetron with reactive cosputtering. XRD studies reveals the crystalline nature of thin films having Dy_2O_3(222) reflection in all samples with Cr_2O_3(116) and CuO(111) reflections in Cr and Cu containing compositions. Field emission scanning electron microscopy demonstrates the homogeneous deposition of thin films with uniform shape, size and distribution of grains. Refractive index, extinction coefficient and absorption coefficient significantly increase while optical reflectance decreases with Cr and Cu mediation corroborating an improved antireflective mechanism. The imaginary part of dielectric constant is found to increase slightly with low tangent loss for Cr containing composition co nsidered favorable for energy storage applications.     

Comparative evaluation of tools for Arabic corpora search and analysis

As the number of Arabic corpora is constantly increasing, there is an obvious and growing need for concordancing software for corpus search and analysis that supports as many features as possible of the Arabic language, and provides users with a greater number of functions. This paper evaluates six existing corpus search and analysis tools based on eight criteria which seem to be the most essential for searching and analysing Arabic corpora, such as displaying Arabic text in its right-to-left direction, normalising diacritics and Hamza, and providing an Arabic user interface. The results of the evaluation revealed that three tools: Khawas, Sketch Engine, and aConCorde, have met most of the evaluation criteria and achieved the highest benchmark scores. The paper concluded that developers’ conscious consideration of the linguistic features of Arabic when designing these three tools was the most significant factor behind their superiority.     

One-pot lithium bromide-catalyzed reaction of polyoxyethylene diglycidyl ether with carbon disulfide: synthesis of new polyoxyethylene epoxyoxathiolane-2-thione

A simple and highly efficient regio- and chemio-specific synthesis of polyoxyethylene epoxyoxathiolan-2-thione was realized from a one-pot reaction of polyoxyethylene diglycidyl ether and carbon disulfide using lithium bromide as a catalyst. The unsymmetrical obtained products were fully characterized by ¹H, ¹³C NMR and high-resolution mass spectra data.