Abstract
Ongoing global population boom has led to the rise in waste and related research on increasing its economic value. In such an attempt, this study aims to activate gas-to-liquids (GTL) derived biosolids (BS) and cardboard (CB) and mixed samples (50:50) using potassium carbonate to produce three activated carbons (ACs): KBS, KCB and KM respectively. The characterization of the samples revealed surface areas of 156, 515, and 527 m2/g for KBS, KCB, and KM, respectively based on Brunauer–Emmett–Teller (BET) analysis, with increased porosity and metal content after activation evident from the Scanning Electron Microscopy-Energy Dispersive Spectroscopy (SEM-EDS) results, as well as the presence of magnetite in the KBS and KM samples apparent from the X-ray powder diffraction (XRD) results. Additionally, Fourier Transform Infrared Spectroscopy (FTIR) results indicate increased C–O–C stretches and O–H bonds after activation of the samples.The ACs were used for methylene blue (MB) removal process which is a rapid for all three samples, reaching equilibrium after 9 h, and optimal at neutral pH and maximum at the highest temperature, 40 °C. The MB adsorption capacity was highest for KM (191.07 mg/g), followed by the KCB and KBS samples. Isotherm modelling of the samples showed best fits for KBS, KCB and KM as Langmuir-Freundlich (LF), Langmuir and Toth models respectively. On the contrary, kinetic modelling using contact time study data for all samples exhibited best fits by the Diffusion-chemisorption (DC) model. Finally, the thermodynamic calculations of the mixed sample disclosed the adsorption process to be exothermic and spontaneous, with potential mechanisms being electrostatic attraction, ion exchange, π-π interactions, and hydrogen bonding. Multiple cycles of KM regeneration was also achieved with good adsorption capacities. Future work will explore other activation methods and examine the magnetic properties of KBS and KM for real water treatment.
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 callDisclaimer: 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.
