RESUMEN
A novel electrothermal swing (ETS) system with gold-electrodeposited activated carbon fiber cloth (GE-ACFC) was developed to adsorb and sustainably recover low-concentration Hg0. GE-ACFC with an Au growth time of 1200 s displayed the largest Hg0 adsorption capacity and >90% removal efficiency. The Hg0 adsorption of GE-ACFC was dominated by physisorption via Au amalgamation. In contrast, Hg adsorption of untreated ACFC (RAW-ACFC) was mainly controlled by physisorption and chemisorption related to carbonyl groups. Nevertheless, both ACFCs could reach 100% ETS Hg0 regeneration. The Hg re-adsorption of GE-ACFC was stable, with efficiency >90% at different regeneration temperatures in three-cycle ETS experiments, but the Hg re-adsorption efficiencies of RAW-ACFC greatly decreased to only 60% after 250 â regeneration, due to the formation of electrothermal hot spots in the ACFC. Because the thermal and electrical conductivity of GE-ACFC increased due to Au electrodeposition, the presence of electrothermal hot spots in GE-ACFC-1200s was minor. Simulation results showed that both pseudo-first-order and pseudo-second-order models fitted well to the desorption patterns of the GE-ACFC. Mass transfer model further suggested that intraparticle diffusion control was the rate-limiting step, with diffusion coefficients increased from the first to the third cycle for GE-ACFC.
