Abstract

Lately, there has been a growing interest in converting low-cost biomass residuals, including wastewater sludge, into char-like materials for various applications. In this research, ammonium (NH4+) adsorption and desorption potential of hydrochar activated via Fenton oxidation were systematically investigated. Hydrochar was prepared from domestic wastewater treatment plant sludge and activated by Fenton oxidation using different H2O2 concentrations, H2O2/Fe2+ ratios, and activation times. The activated hydrochars (AHs) were characterized by ATR-FTIR, high-resolution XPS, BET specific surface area, and SEM, and their NH4+ adsorption capacity was analyzed. The NH4+ adsorption isotherms and kinetics, adsorption in the presence of competing ions (with and without humic acid), and NH4+ desorption were investigated. The results show that following hydrochar activation, the acidic groups’ concentration and the BET surface area increased, but the morphology remained essentially unchanged. It was also found that the activation occurs within a few minutes when using a relatively low concentration of reagents, and without extensive post-treatment steps. The NH4+ adsorption onto AH at equilibrium fitted the Langmuir isotherm model, with a maximum adsorption capacity of 30.77 mg g−1, and the NH4+ adsorption kinetics fitted the pseudo-second-order model. NH4+ adsorption in the presence of competing ions decreased by up to 33 ± 3%. NH4+ desorption experiments demonstrated that NH4+ recovery can reach 33 ± 5% with ultrapure water and 67 ± 2% with 2 M KCl. The results of this study indicate that Fenton oxidation is a promising alternative for hydrochar activation, and can be used as an adsorbent for NH4+ remediation in wastewater treatment processes.

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.