Abstract

This inquiry focuses on acquiring empirical models to predict ciprofloxacin removal using magnetization of functionalized multi-walled carbon nanotubes (FMWCNTs-Fe3O4) from an aqueous solution. The response surface methodology (RSM) and support vector regression (SVR) as data mining techniques were adopted to develop models. Critical parameter effects comprising pH (3−10), adsorbent dose (0.2–1 g/L), contact time (5–60 min) and ciprofloxacin concentrations (30–100 mg/L) were analysed. The Langmuir, Freundlich, Temkin and Dubinin-Radushkevich isothermal models were utilized to fit the empirical data. FMWCNTs-Fe3O4 prepared by chemical co-precipitation method was loaded by Fe3O4 nanoparticles (using sonication) to synthesize functionalized multi-walled carbon nanotubes to remove ciprofloxacin (CIP). FMWCNTs-Fe3O4 were characterized by fourier transform infrared spectroscopy (FTIR), X-Ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), vibrating sample magnetometer (VSM) methods. The Langmuir model was utilized to precisely describe the maximum adsorption capacity(qmax) of 107.66 mg/g with R2 = 0.998. In this study, the pseudo-second-order model exactly described the adsorption process(R2 = 0.99). The results illustrated that the LSSVM (least squares support vector machine) model efficiently predicted the CIP removal percentage with very high accuracy in the training phase (R2 = 0.975) and the test phase (R2 =0.970). Moreover, the highest removal percentages in optimized step were achieved for RSM (pH 5.4, dose 0.78 g/L, time of 24.5 min, and CIP concentrations of 59 mg/L) and GA (genetic algorithm) (pH 4.4, dose 0.74 g/L, time of 42 min, and CIP concentrations of 38 mg/L) techniques by 88% and 99.1%, respectively. The FMCNTs-Fe3O4 efficiency has decreased by 12% even after five used cycles relative to the optimal conditions (regeneration). Therefore, FMWCNTs-Fe3O4 adsorption was considered to be an effective technique for CIP removal in the aqueous environment.

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