Nitrogen-doped activated carbon composite electrode for deionization of phosphate removal and DFT model adsorption of phosphates

Phosphate discharge in sewage can result in water eutrophication, posing a threat to aquatic ecosystems. Membrane capacitive deionization (MCDI) has demonstrated outstanding performance and significant potential for salt removal and nutrient recovery. In this study, a nitrogen-doped activated carbon electrode material (NAC) was synthesized through one-step pyrolysis to selectively remove phosphate from MCDI. At a voltage of 1.2V, a flow rate of 20 mL/min, and a pH of 6.51, the phosphate adsorption capacity of the NAC electrode was determined to be 1.60 mg/g. The study revealed that NAC pHpzc increased from 4.14 to 6.44, effectively broadening the pH range for phosphate removal. In the presence of competing ions (NO3−, Cl−, and SO42−) at a concentration of 0.5 M, the electroadsorption capacity of phosphate decreased to 1.21 mg/g, 1.14 mg/g, and 1.02 mg/g, respectively. The kinetic parameters of adsorption indicated that NAC electroadsorbed phosphate through physical adsorption, with the maximum adsorption capacity achieved at 303K. Data from the Freundlich isothermal model suggested that phosphate adsorption by the NAC electrode involves a multilayer adsorption process. A carbon structure model of density functional theory (DFT), incorporating doped nitrogen, was constructed based on XPS analysis. Following nitrogen doping, the electrostatic potential (ESP) of unsaturated carbon atoms became more positive, enhancing the ability of nitrogen-doped activated carbon to adsorb phosphate. This study provides compelling evidence that nitrogen doping facilitates the adsorption of phosphate by carbon materials. [Display omitted] •The MCDI composite electrode had a nitrogen-doped carbon electrode.•NAC's 10 mg/L phosphate adsorption in MCDI was 1.60 mg/g.•In MCDI, coexisting ions affected phosphate removal: SO42− > Cl− > NO3−.•The DFT model for phosphate adsorption shows nitrogen doping benefits.