Abstract

The current study emphasises on sorptive expulsion of phenol from aqueous solution using ortho-phosphoric acid (STAC-O) and sulphuric acid (STAC-H)-activated biochar derived from spent tea waste. STAC-O and STAC-H were instrumentally anatomised using scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), BET surface area and thermal gravimetric analyser. Equilibrium and kinetic data were implemented for the investigative parametric batch study to prospect the influence of adsorbent dosage, contact time, initial concentration and pH for eradication of phenol from aqueous solution. The maximum phenolic removals by STAC-O and STAC-H are 93.59% and 91.024% respectively at the parametric conditions of adsorbent dosage 3g/l time 2h, initial phenol concentration 100mg/l and pH8. Non-linear regression of adsorption isotherms and kinetics was accomplished using the equilibrium data. Both the specimens were compared, and it delineated that Temkin isotherm model is contented. The maximum adsorption intakes for STAC-H and STAC-O were 185.002mg/g and 154.39mg/g respectively. Pseudo-second-order kinetic model was best fitted for portraying the chemisorption phenomena. Boyd kinetic and intra-particle diffusion model were investigated to elucidate the diffusion mechanism involved in the process. Desorption study was employed for determining the regeneration proficiency of the adsorbents using water, ethanol and NaOH with maximum 93% and 51.16% extrusion for STAC-O and STAC-H respectively. The process parameters involved in this study were further analysed using artificial neural network perusal to determine the input-output relationships and data pattern. The overall adsorption study along with cost estimation exhibited that bidirectional activation of spent tea biochar was prospective in abatement of phenol from aqueous media.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.