Abstract

A highly efficient adsorbent functionalized with phosphate groups made from a local agricultural waste, ramie stalk, was designed for Zn2+ removal from water. SEM, EDS, FTIR, zeta potential, and XPS tests were used to study the morphology and properties of modified ramie stalk (RS-P). The results showed that the phosphate groups were successfully grafted to the surface of the ramie stalk, which has a multilayered and porous structure and can provide large adsorption sites. Adsorption performance and mechanism were investigated in the static and dynamic adsorption experiments. The adsorption kinetics of Zn2+ by RS-P were better fitted by the pseudo-second-order model, indicating chemical adsorption. Adsorption isotherm was better described by Redlich-Peterson isotherm, which suggested heterogeneous and multi-site adsorption, with a maximum adsorption capacity of 0.558mmolg-1. The characterization of adsorbents before and after adsorption indicated that a combined action of electrostatic interaction and ion exchange was the primary mechanism of adsorption. Dynamic adsorption experiments with fixed-bed column displayed excellent water treatment capabilities. RS-P exhibited good reusability in 5 cycles without much deterioration in its adsorption performances. Complex co-existing ions impaired Zn2+ adsorption during real wastewater treatment. This research benefits agricultural waste recycling and provides safe water to ensure economic, social, and environmental sustainability.

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.