Removal efficiency and adsorption mechanisms of CeO2 nanoparticles onto granular activated carbon used in drinking water treatment plants

• DOI: 10.1016/j.scitotenv.2022.159261
• Publication Date: 2022-10-05T23:28:53Z
• Authors: Lina Ramirez Arenas; Philippe Le Coust...; Stéphan Ramseier ...; Stéphane Zimmermann; Serge Stoll
• Keywords: info:eu-repo/classification/ddc/333.7-333.9; info:eu-repo/classification/ddc/550; Activated carbon; Adsorption isotherms; 01 natural sciences; Water Purification; Kinetics; Adsorption kinetics; Charcoal; Humans; Nanoparticles; Adsorption; Water Pollutants, Chemical; 0105 earth and related environmental sciences

The presence of NPs in drinking water resources raises a global concern on their potential risk for human health, and whether or not drinking water treatment plants are able to effectively remove NPs to prevent their ingestion by humans. In this study, we investigate the efficiency of granular activated carbon (GAC), commonly used in conventional municipal water treatment processes, for the removal of CeO2 NPs. In ultrapure water, NPs are found to have a good affinity for GAC and results indicate an increase in the adsorption capacity from 0.62 ± 0.10 to 5.05 ± 0.51 mg/g, and removal efficiency from 35 % ± 4 to 54 % ± 5 with increasing NPs concentration. Kinetic studies reveal that intraparticle diffusion is not the only rate controlling step indicating that mass transfer effect is also playing a role. Adsorption mechanisms are mainly controlled by the electrostatic attractions between the positively charged NPs and negatively charged GAC. Although electrostatic conditions in Lake Geneva water are less favorable for NPs adsorption, the adsorption capacity and removal efficiency are higher than in ultrapure water with values raising from 0.41 ± 0.17 to 7.13 ± 1.13 mg/g and 26 % ± 8 to 75 % ± 11, respectively. Furthermore, the external mass transfer process onto GAC surface is more important than for ultrapure water. NPs adsorption mechanism is explained by the presence of divalent cations and natural organic matter (NOM) which promote the formation of CeO2 NPs-NOM-divalent cation heteroaggregates increasing both adsorption and removal efficiency by cation bridging.