Abstract

The re-utilization of food waste is an eco-friendly method for valorizing waste. In this study, food waste was blended with iron (Fe-FW) and optimized using the response surface methodology (RSM) to produce Fe-loaded food waste biochar (Fe-FWB); moreover, the waste was utilized to probe the adsorption of phosphate in water, where pyrolysis time (1.0, 2.5, and 4.0 h), temperature (300, 450, and 600 °C), and Fe concentrations (0.1, 0.3, and 0.5 M) were set as independent variables. After optimizing the Fe-FWB, batch experiments were performed to examine the phosphate sorption characteristics of Fe-FW and Fe-FWB. A pseudo-second order and Elovich kinetic model thoroughly explained the adsorption kinetics, which was indicative of the rate-limited sorption via diffusion or surface coverage after the rapid initial adsorption. The Freundlich and Redlich–Peterson isotherm models more accurately simulated the adsorption of phosphate onto Fe-FW and Fe-FWB than the Langmuir isotherm model. The thermodynamic results presented a positive value of ΔG0, clearly indicating that the reaction was not spontaneous; positive values of ΔH0 and ΔS0 affirmed the endothermic characteristic of phosphate uptake into Fe-FW and Fe-FWB, with an increase in randomness. The adsorption of phosphate onto Fe-FW and Fe-FWB decreased as the solution pH increased from 3 to 11. In the presence of interfering anions, phosphate adsorption onto Fe-FWB was influenced by the coexistence of HCO3-, SO42-, and NO3−. These results suggest that the synthesized Fe-loaded food waste biochar can be used as an emerging adsorbent for phosphate removal from aqueous solutions.

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