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In the sight of the ever-increasing significance of green-based iron nanoparticles especially in wastewater treatment applications is a compelling reason for their use in a waste prevention opportunity, safer environment and benign precursor materials become the vital considerations. Hence, in the current investigation, an efficient co-precipitation technique was applied to prepare highly active chitosan-coated magnetic iron oxide that is applied for wastewater remediation. In the current investigation, chitosan coupled with magnetite nanoparticles namely CS-M was attained by coupling chitosan (CS) with magnetite nanoparticles via simple co-precipitation in different weight proportions and the attained samples labeled as CS-M-(2:1), CS-M-(3:1) and CS-M-(1:2). The structure, morphology and characteristics of the prepared samples were characterized using X-ray diffraction spectroscopy and transmission electron microscopy (TEM). The catalytic oxidation activity of the prepared samples was investigated to eliminate Basic Blue 9 (BB9) dye from aqueous effluent as simulated textile polluted stream. The experimental data exposed almost BB9 dye emanation. The system parameters revealed the maximal BB9 oxidation (99%) was attained within 2 h of irradiance time. Box–Behnken design factorial design based on response surface methodology was applied to optimize the Fenton’s system (CS-M-(2:1)/H2O2) parameters to maximize the efficiency 2.4 and 767 mg/L of CS-M and H2O2, respectively, at pH 7.0. The experimental data exposed that CS-M-(2:1) is signified as the optimal catalyst mixture. The kinetic data verify the oxidation system follows the second-order reaction kinetic model. Further, thermodynamic variables predicted that the reaction is endothermic and non-spontaneous in nature. Hence, the catalyst could be environmental benign and the evaluation introduces the role of engineers and chemists in a world for a sustainable material use.

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Different metal catalysts have been tested for the one-pot transformation of carbonyl compounds, amines and phosphites to α-aminophosphonates. The influence of catalyst type, amount, solvent and the substrate electronic factor have been investigated. The results revealed that the carbonyl compounds could be smoothly converted into α-aminophosphonates at room temperature in good to excellent yields, with or without solvent in a reasonable reaction time. These results suggested that among others, lithium perchlorate and metal triflates were proven to be effective catalysts in 10 moles % catalysts. Polar aprotic solvents proved to be the best for the synthesis of α-aminophosphonates. The synthesized compounds' structure characterizations were elucidated by different spectroscopic tools and showed results consistent with the expected structures.