Publications by authors named "K Katin"

The study presents the fabrication and superior photoactivity of a ternary g-CN/FeVO/AgBr heterojunction nanocomposite, synthesized via a chemical precipitation method for effective degradation of tetracycline (TC) and Victoria Blue (VB) dye under light illumination. The morphology and the crystal size of the synthesized nanocomposite were characterized by using FESEM and XRD and the calculated grain size (100.39 nm) is larger than the crystal size (48.

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Context: This study addresses the development of sustainable pyridinium ionic liquids (ILs) because of their potential applications in agriculture and pharmaceuticals. Pyridinium-based ILs are known for their low melting points, high thermal stability, and moderate solvation properties. We synthesized three novel pyridinium-based ILs: 1-(2-(isopentyloxy)-2-oxoethyl)pyridin-1-ium chloride, 1-(2-(hexyloxy)-2-oxoethyl)pyridin-1-ium chloride, and 1-(2-(benzyloxy)-2-oxoethyl)pyridin-1-ium chloride.

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Keeping recruitment of green and cost-effective solutions for environmental challenges in view, the current work was designed to solve the problems related to metal corrosion in the aqueous phases of crude oil in chemical industries. Green materials can play an important role in protecting metals from this corrosion. Hence, the green anti-corrosion material based upon gossypol derivate is suggested to solve the above problems.

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We describe here the fabrication of large-area molecular junctions with a configuration of ITO/[Ru(Phen)]/Al to understand temperature- and thickness-dependent charge transport phenomena. Thanks to the electrochemical technique, thin layers of electroactive ruthenium(II)-tris(phenanthroline) [Ru(Phen)] with thicknesses of 4-16 nm are covalently grown on sputtering-deposited patterned ITO electrodes. The bias-induced molecular junctions exhibit symmetric current-voltage (j-V) curves, demonstrating highly efficient long-range charge transport and weak attenuation with increased molecular film thickness (β = 0.

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Cancer is a disease that occurs as a result of abnormal or uncontrolled growth of cells due to DNA damage, among many other causes. Certain cancer treatments aim to increase the excess of DNA breaks to such an extent that they cannot escape from the general mechanism of cell checkpoints, leading to the apoptosis of mutant cells. In this study, one of the Sarco-endoplasmic reticulum CaATPase (SERCA2a) inhibitors, Istaroxime, was investigated.

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