Journal
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
Volume 28, Issue 22, Pages 28289-28306Publisher
SPRINGER HEIDELBERG
DOI: 10.1007/s11356-021-12497-6
Keywords
Quartz; SiO2; Nanoparticles; (3-Aminopropyl)trimethoxysilane; Glutaraldehyde; Polyethylenimine; Schiff base; Rhodamine B; Flooding; Degradation
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The study successfully prepared a SiO2/PEI-Cu(II) composite by modifying the surface of quartz nanoparticles, and explored its application in the oxidative degradation of RhB dye. Experimental results showed that the composite exhibited good stability and catalytic activity, efficiently degrading the dye.
The study describes the loading of the quartz SiO2 nanoparticles (NPs) with (3-aminopropyl)triethoxysilane (APTES) linker with simultaneous lengthening of the linker through the terminal amine group by glutaraldehyde (GA). The reactive polyethylenimine (PEI) was introduced to the surface to increase the ability to capture Cu(II) ions. The composite got the abbreviation SiO2/PEI-Cu(II). The Cu(II) ions were the active center with a peroxo-complex activation state. The composite characterization included scanning electron microscopy (SEM), transmission electron microscopy (TEM), electron-dispersive X-ray analysis (EDX), Fourier transform infrared spectroscopy (FT-IR), X-ray powder diffraction (XRD), thermogravimetric analysis (TGA), and Brunauer-Emmett-Teller (BET) surface analyzer. The kinetics of the oxidative degradation of Rhodamine B (RhB) dye obeyed the pseudo-first order under flooding conditions. The reaction parameters including the catalyst dose, solution pH, initial concentration of reactants, and temperature got some attention. The obtained results showed that more than 91.7 +/- 1% of RhB dye was degraded to CO2, NH4+, NO3-, H2O, and some inorganic acids after 30 min as confirmed by gas chromatography mass spectrometry and total organic carbon (TOC) measurements. Also, GC-MS spectra for water samples drawn from the reaction in successive periods had suggested a conceivable degradation pathway for RhB by hydroxyl radicals. Degradation starts with de-alkylation then carboxyphenyl removal followed by two successive ring-opening stages. Both the effects of the catalyst recycling and treated water reusability on the reaction rate were studied. The catalyst provided noticeable stability over three consecutive cycles.
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