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The dust grain surface potential is examined analytically and numerically in dusty plasmas containing negative/positive ion species by using the Cairn Tsallis (non-Maxwellian) dusty plasma. The equations for the dust-charging process are derived to solve the current balance equation for the xenon–fluorine–sulfur hexafluoride and argon–fluorine–sulfur hexafluoride plasmas. The charging process affected by plasma properties such as spectral indices α and q, in addition to positive ion streaming ( U A r + and U X e + ) and negative ion streaming ( U F − and U S F 6 − ) of both types of plasmas, is examined. Our findings suggest that considering a wide range of X e + − F − − S F 6 − and A r + − F − − S F 6 − masses is critical for understanding plasma physics, specifically multi-component plasmas. [ABSTRACT FROM AUTHOR]

This study used a supported liquid membrane system (SLM) using Celgard 2400 polypropylene as the support, di(2-ethylhexyl) phosphoric acid (D2EHPA) as the carrier, and kerosene as the diluent. To obtain the best carrier concentration, D2EHPA concentrations between 0.04 and 0.6 M were used. The Cr (III) solutions used in the feed phase had various ionic strengths and were adjusted with NaCl at concentrations ranging from 0.25 to 1.75 M. To maintain a constant pH (4) in the feed phase, a 0.2 M acetic acid–sodium acetate buffer was utilized. Because the rate of Cr (III)-carrier complex formation at the interface of the feed solution and membrane increased up to 20 × 10−4 mol/L, it was discovered that transport of Cr (III) rose with an increase in chromium content in the feeding phase. For the optimization of the various stripping agents, HCl concentration was employed, from 0.25 M to 1.75 M. It was observed that Cr (III) transport increased with the increase in HCl concentration because the transport was at a pH gradient, which was the main driving force. Because of the fact that at the feed phase-membrane contact, D2EHPA combined with chromium ions to form the Cr (III)-carrier complex and released H+ protons, in the feed phase, the Cr (III)-carrier complex was diffused into a stripping phase, wherein Cr (III) ions were stripped and the carrier was reversibly protonated again. [ABSTRACT FROM AUTHOR]

Amylase and glucosidase enzymes are the primary harmful source in the development of the chronic condition known as diabetes mellitus. The main function of these enzymes is to break the macromolecules into simple sugar units which are directly involved in the solubility of blood, hence increasing blood glucose levels. To overcome this effect, there is a need for a potent and effective inhibitor that inhibits the conversion of macromolecules of sugar into its smaller units. In this regard, we synthesized thiazolidinone-based indole derivatives (1–20). The synthesized derivatives were evaluated for α-amylase and α-glucosidase inhibitory activity. Different substituted derivatives were found with moderate to good potentials having IC50 values ranging, for α-amylase, from 1.50 ± 0.05 to 29.60 ± 0.40 μM and, for α-glucosidase, from IC50 = 2.40 ± 0.10 to 31.50 ± 0.50 μM. Among the varied substituted compounds, the most active analogs four (1.80 ± 0.70 and 2.70 ± 0.70), five (1.50 ± 0.05 and 2.40 ± 0.10, respectively) of the series showed few folds better inhibitory activity than standard drug acarbose (IC50 = 10.20 ± 0.10 and 11.70 ± 0.10 μM, respectively). Moreover, structure–activity relationship (SAR) was established and binding interactions were analyzed for ligands and proteins (α-amylase and α-glucosidase) through a molecular docking study. [ABSTRACT FROM AUTHOR]

By using the chemical bath deposition approach, binary bismuth sulphides (Bi2S3) and chromium-doped ternary bismuth sulphides (Bi2−xCrxS3) thin films were effectively produced, and their potential for photovoltaic applications was examined. Structural elucidation revealed that Bi2S3 deposited by this simple and cost-effective method retained its orthorhombic crystal lattice by doping up to 3 at.%. The morphological analysis confirmed the crack-free deposition, hence making them suitable for solar cell applications. Optical analysis showed that deposited thin films have a bandgap in the range of 1.30 to 1.17 eV, values of refractive index (n) from 2.9 to 1.3, and an extinction coefficient (k) from 1.03 to 0.3. From the Hall measurements, it followed that the dominant carriers in all doped and undoped samples are electrons, and the carrier density in doped samples is almost two orders of magnitude larger than in Bi2S3. Hence, this suggests that doping is an effective tool to improve the optoelectronic behavior of Bi2S3 thin films by engineering the compositional, structural, and morphological properties. [ABSTRACT FROM AUTHOR]

Spent Ni–Cd batteries are now considered an important source for many valuable metals. The recovery of cadmium, cobalt, and nickel from spent Ni–Cd Batteries has been performed in this study. The optimum leaching process was achieved using 20% H2SO4, solid/liquid (S/L) 1/5 at 80 °C for 6 h. The leaching efficiency of Fe, Cd, and Co was nearly 100%, whereas the leaching efficiency of Ni was 95%. The recovery of the concerned elements was attained using successive different separation techniques. Cd(II) ions were extracted by a solvent, namely, Adogen® 464, and precipitated as CdS with 0.5% Na2S solution at pH of 1.25 and room temperature. The extraction process corresponded to pseudo-2nd-order. The prepared PTU-MS silica was applied for adsorption of Co(II) ions from aqueous solution, while the desorption process was performed using 0.3 M H2SO4. Cobalt was precipitated at pH 9.0 as Co(OH)2 using NH4OH. The kinetic and thermodynamic parameters were also investigated. Nickel was directly precipitated at pH 8.25 using a 10% NaOH solution at ambient temperature. FTIR, SEM, and EDX confirm the structure of the products. [ABSTRACT FROM AUTHOR]

Amylase and glucosidase enzymes are the primary harmful source in the development of the chronic condition known as diabetes mellitus. The main function of these enzymes is to break the macromolecules into simple sugar units which are directly involved in the solubility of blood, hence increasing blood glucose levels. To overcome this effect, there is a need for a potent and effective inhibitor that inhibits the conversion of macromolecules of sugar into its smaller units. In this regard, we synthesized thiazolidinone-based indole derivatives (1−20). The synthesized derivatives were evaluated for α-amylase and α-glucosidase inhibitory activity. Different substituted derivatives were found with moderate to good potentials having IC50 values ranging, for α-amylase, from 1.50 ± 0.05 to 29.60 ± 0.40 μM and, for α-glucosidase, from IC50 = 2.40 ± 0.10 to 31.50 ± 0.50 μM. Among the varied substituted compounds, the most active analogs four (1.80 ± 0.70 and 2.70 ± 0.70), five (1.50 ± 0.05 and 2.40 ± 0.10, respectively) of the series showed few folds better inhibitory activity than standard drug acarbose (IC50 = 10.20 ± 0.10 and 11.70 ± 0.10 μM, respectively). Moreover, structure−activity relationship (SAR) was established and binding interactions were analyzed for ligands and proteins (α-amylase and α-glucosidase) through a molecular docking study.