Published: CABEQ 35 (3) (2021) 225-250
Paper type: Original Scientific Paper
A. Naz, S. Arun, R. Kumari, S. S. Narvi and M. S. Alam
Abstract
A novel and efficacious inorganic-organic hybrid material was synthesized by immobilizing Cu(II)-Schiff’s base complex on silica-gel using 3-(2-aminoethylamino) propyltrimethoxysilane as linker and 1,3-diphenyl-1,3-propanedione for Schiff’s base formation. The hybrid was characterized by FT-IR, DRUV-Vis, Solid State 13C CPMAS
NMR, Powder-XRD, SEM, ICP-AES, EDX and TGA and EPR techniques. Catalytic
ability of the hybrid was evaluated for oxidative degradation of Reactive Black 5, and
oxidation of few representative organic substrates, viz., tetralin, cyclohexane, cyclohexanol, and cyclopentanol, where the hybrid catalyst decomposes H2O2 to generate ·OH free radicals. Influence of various reaction parameters, i.e., H2O2
concentration, catalyst concentration, and temperature, on dye degradation process was studied and best reaction conditions for maximum degradation of RB5 were also determined. The catalyst gave a high dye degradation efficiency of 91 %, and a good product yield of 42.61 %, 41.09 %, 40.54 %, and 38.44 % for conversion of tetralin (with selectivity of 74.23 % and 25.77 % for tetralone and tetralol, respectively), cyclohexane (with selectivity of 75.05 % and 24.95 % for cyclohexanone and cyclohexanol, respectively), cyclohexanol (with 100 % selectivity for cyclohexanone), and cyclopentanol (with 100 % selectivity for cyclopentanone), respectively. Easy separation, reusability, and good catalytic activity leading to possible development of eco-friendly industrial manufacturing process are the motivating factors for using the synthesized novel material.
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Keywords
inorganic-organic hybrid, silica gel, catalysis, Reactive Black 5, hydrogen peroxide