Influence of Mg-substitution on structural and electrical properties of ion-conducting Ca-doped tri-yttrium gallate

The signature of oxide ion conductivity was perceived in acceptor-doped (alkaline-earth metals) Y₃GaO₆. An acceptor doping of 2%Ca in Y₃GaO₆ (i.e., Y_2.94Ca_0.06GaO₆) has been found to exhibit a remarkable conductivity. The present work examines the conductivity behavior of 2% Ca-doped tri-yttrium gallate (Y_2.94Ca_0.06GaO₆) and also the effect of Mg-substitution on the phase formation and electrical conductivity of Y_2.94Ca_0.06GaO₆ for its possible application as a solid electrolyte. Polycrystalline dense ceramic samples of Y_2.94Ca_0.06Ga_1−xMg_xO_6−δ (with x = .00–.04) were fabricated using the conventional solid-state reaction route. The X-ray diffraction patterns were recorded to confirm the phase formation. The solid solubility limit of Mg²⁺ at Ga³⁺ site was found for x < .03. All the samples were observed to exhibit orthorhombic structure with Cmc21 symmetry (ICSD no.: 155086). Scanning electron microscopy (SEM) morphology reveals dense polygonal grains with vibrant grain boundaries. A significant increase in the conductivity is observed by substituting 1 mol% of Mg²⁺ at the Ga³⁺ site of Y_2.94Ca_0.06Ga_1−xMg_xO_6−δ. However, a further addition of higher dopant concentration of Mg²⁺ leads to a decline in the electrical conductivity. A relationship between the dopant concentration, phase formation, and structural characterizations has been established to analyze the conductivity behavior.     

Polymer interface changes in electrophoretic deposition

A Monte Carlo computer simulation model for the electrophoretic deposition of polymer chains on a discrete lattice is used to study the polymer density profile, interface growth, and its dependence on field, temperature, and molecular weight. The interface width (W) decreases WE^−1/2 on increasing the field (E). Width (W) depends non-monotonically on the temperature (T): a power-law decay is followed by a power-law increase on raising the temperature. Monotonic decay of the interface width with the molecular weight is possibly a stretched exponential. Conformation and dynamics of a tracer chain is used to probe its characteristics in interface to bulk region. The root mean square (rms) displacement of the center of mass of the tracer chain shows an ultra-slow motion, Rt^ν (ν0.1–0.01 at E=0.1–1.0) as the driven chain moves deeper from interface to bulk. Longitudinal compression of the radius of gyration (R_g) of the chain increases with the field; transverse components (R_gx, R_gy) are larger than the longitudinal component (R_gz). The transverse component (R_gx(y)) becomes oscillatory due to periodic squeezing at high fields as the field competes with the polymer barriers.     

Studies on high-performance blended/multiblended cements and their durability characteristics

Number of blends were prepared by intergrinding clinker, gypsum, fly ash, calcined clay, microsilica and limestone in laboratory ball mill in varying percentages, and their physical properties such as fineness, consistency, setting time and compressive strength have been determined. The durability tests on selected compositions were also conducted by exposing the mortar cubes separately in 5% Na₂SO₄ and 5% NaCl solutions till the age of 90 and 180 days. The performance was observed by compressive strength development criteria after various length of exposure. Results have been discussed and found that the durability of blended cement is higher than the ordinary Portland cement.     

Electrochemical treatment of cotton textile-based dyeing effluent

The electrochemical treatment (ECT) of textile wastewater was carried out in a 1.5 dm³ electrolyte batch reactor using iron electrodes. With the four plate configurations, a current density (CD) of 89.2 A/m² and a pH value of 8.5 were found to be optimal, at which maximum reduction in chemical oxygen demand (COD) and colour achieved were 86% and 79%, respectively. Loss of 0.0666 kg/m³ iron electrode and 18.44 kWh/m³ power consumption was observed during ECT with a maximum COD reduction of 79%. The settling characteristics of electrochemically treated effluents as well as the characteristics of foam and residue were also analysed.     

Cerium-containing MCM-41 materials as selective acylation and alkylation catalysts

The synthesis of Ce–MCM-41, Al–MCM-41 and Ce–Al–MCM-41-type mesoporous materials was carried out hydrothermally by refluxing the gel with magnetic stirring under atmospheric pressure for 24–36 h. The samples were characterized thoroughly in order to obtain the structural and textural properties, which reveal the presence of well-ordered M41S-type materials. The Ce–MCM-41 samples were used for catalytic acylation of alcohols, thiols, phenols and amines show good activity and selectivity including high chemoselectivity towards selective monofunctional acylation of bifunctional compounds. Quite importantly the acylation of bulky molecules such as cholesterol, ergesterol and β-sitosterol could be achieved using Ce–MCM-41 as solid catalyst. The presence of Ce along with Al in Ce–Al–MCM-41 was found to have synergistic effect as Ce–Al–MCM-41samples were more active catalysts for alkylation of naphthalene compared to either Ce–MCM-41 or Al–MCM-41 with comparable Si/Al or Si/Ce molar ratio.     

An in-Depth Analysis of the Swelling,Mechanical, Electrical,and Drug Release Properties of Agar–Gelatin Co-Hydrogels

Agar–gelatin-based co-hydrogels were prepared with different compositions of the agar and the gelatin fractions. The intermolecular hydrogen bonding was higher in the co-hydrogels as compared to the gelatin hydrogel. Swelling studies indicated diffusion-mediated swelling. The electrical stability of the co-hydrogels was higher as compared to the gelatin hydrogel. Though the firmness of the co-hydrogels was higher, Weichert model of viscoelasticity indicated that the inherent mechanical stability of the gelatin hydrogel was superior. The release of ciprofloxacin hydrochloride was predominately Fickian diffusion-mediated. In gist, the co-hydrogels can be tried as polymeric constructs for controlled drug delivery applications.     

Insight on Castor Oil Based Polyurethane and Nanocomposites: Recent Trends and Development

Castor oil has gained momentous attention as a valuable bio-based monomer and a potential alternative to the current petrobased polyol for synthesizing polyurethane due to the presence of inherent hydroxyl group. In spite of its huge potentiality very little has been reviewed regarding the development of polyurethane from castor oil. This review thus highlights the recent trends and development in the field of polyurethane and its nanocomposite based on castor oil including its biodegradability and weatherability studies. Further, this review also provides an insight regarding the utilization of castor oil based polyurethane and its nanocomposite for coating application.     

Reactivity of Hydroxamate Ions in Cationic Vesicular Media for the Cleavage of Carboxylate Esters

The hydrolysis of carboxylate esters viz. p‐nitrophenyl acetate (PNPA), p‐nitrophenyl butyrate (PNPB) and p‐nitrophenyl octanoate (PNPO) in the presence of cationic vesicles of the surfactant dioctadecyldimethylammonium bromide (DODAC) by different hydroxamate ions i.e. acetohydroxamate (AHA^?), benzohydroxamate (BHA^?) and salicylhydroxamate (SHA^?) were studied. The kinetic data was supported by spectrophotometric measurements. The effects of vesicular size on the reaction have been discussed. The differential reactivity under endo‐ and exovesicular conditions has also been evaluated. Critical vesicle concentrations (CVC) of cationic vesicular surfactants were determined from conductometric and fluorimetric measurements at 300 K. Fluorescence probe pyrene and pyrene‐1‐carboxaldehyde have been used for determination of CVC. Further, thermodynamic parameters viz. Standard Gibb's energy (?G°), enthalpy (?H°), and entropy (?S°) of vesicles has also been evaluated within a temperature range of 303.15–328.15 K.     

Physiochemical Properties of Gamma-Irradiated Tri-iso-amyl Phosphate–Dodecane System: Effect of Aqueous Phase Acidity

ABSTRACT

Tri-iso-amyl phosphate (TiAP) in dodecane (DD) is emerging as a potent alternative for the extraction of suitable actinides from nitric acid solutions comprising various metal ions. A detailed investigation on the evolution in physicochemical properties upon gamma irradiation of TiAP-DD system has been carried out. Physical properties, such as density, viscosity, phase disengagement time, interfacial tension, etc., were measured for neat as well as irradiated solvent phases. Effect of aqueous phase acidity, which is an important parameter during extraction, on the hydrodynamic properties of the solvent during radiolysis was compared. ATR–FTIR spectroscopy of the irradiated phase was compared to find out the formation of new classes of compounds, if any.