Carbon aerogel (CA) has a rich porous structure, in which micropores and mesopores provide a huge specific surface area to form electric double layers. This property can be applied to the application of capacitive deionization (CDI). The adsorption effect of CA electrode on Cu²⁺ in an aqueous solution was explored for solving heavy metal water pollution. The CAs were synthesized by a sol-gel process using an atmospheric drying method. The structure of CAs was characterized by scanning in an electron microscope (SEM) and nitrogen adsorption/desorption techniques. The adsorption system was built using Cu²⁺ solution as the simulation of heavy metal pollution solution. The control variate method was used to investigate the effect of the anion species in copper solution, the molar ratio of resorcinol to catalyst (R/C) of CA, and the applied voltage and concentration of copper ion on the adsorption results.

Capacitive deionization (CDI) technology possessing excellent desalination performance and energy efficiency is currently being widely studied in seawater desalination. In this work, the graphene–composite carbon aerogels (GCCAs) easily prepared by an ambient pressure drying method served as electrodes to remove salt ions in aqueous solution by CDI. The microstructure of the obtained GCCAs was found to depend on the component content in the precursor solution, and could be controlled through varying the mass ratio of resorcinol and formaldehyde to graphene oxide (RF/GO). The surface characteristics and microstructure of GCCAs were characterized by Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). In addition, the electrochemical tests and CDI experiments of GCCA electrodes were conducted in NaCl solution. Thanks to the reasonable pore structure and highly conductive network, GCCA-150 achieved the best salt adsorption capacity of 26.9 mg/g and 18.9 mg/g in NaCl solutions with concentrations of 500 mg/L and 250 mg/L, respectively.