Dana A. Kader , Safin A. Abdalla , Sewara J. Mohammed , Dara Muhammed Aziz , Dlzar D. Ghafoor , Trefa M. Abdullah , Nian N.M. Agha , Fryad S. Mustafa , Sangar Ali Hassan
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引用次数: 0
Abstract
For the first time, this work demonstrates an environmentally benign and sustainable catalytic process using a TiO2@PPHs nanocomposite prepared by green synthesis. This was achieved by preparing a nanocomposite by decorating TiO2NPs with polyphenols (PPHs) extracted from black carrots (Daucus carota), which resulted in an active photocatalyst for oxidation reactions and Brilliant Green (BG) dye degradation under visible light (green LED light). The prepared TiO2@PPHs nanocomposite was comprehensively characterized by XRD, SEM, FT-IR, EDX, and BET analysis for pore-size distribution and specific surface area measurement. Zeta potential measurement and UV–visible DRS spectroscopy were also conducted. XRD and SEM with EDX analysis confirmed the crystallinity of the TiO2@PPHs nanocomposite with a particle size of 67.92 nm. Surface interactions and improved optical properties with a reduction in band gap energy from 3.04 for pure TiO2NPs to 2.02 eV for TiO2@PPHs nanocomposite make it a suitable catalyst that can be activated under green light irradiation. The catalytic activity of TiO2@PPHs was studied for the aerobic oxidation of amine to imines and degradation of BG dye in aqueous solution. The nanocomposite showed excellent efficiency in amine oxidation (up to 99 % conversion) and dye degradation (96 %). Mechanistic studies confirmed the significant role of the generated ROS, in particular hydroxyl and superoxide radicals, during these photocatalytic reactions. The TiO2@PPHs catalyst also exhibited recycling sequences with stable efficient synergistic catalytic results, which highlights light on sustainability in industrial applications.
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.