Changes in adsorption mechanisms of radioactive barium, cobalt, and strontium ions using spent coffee waste biochars via alkaline chemical activation: Enrichment effects of O-containing functional groups.

Environ Res

Department of Integrated Energy and Infra system, Kangwon National University, Kangwondaehak-gil, 1, Chuncheon-si, Gangwon-do, 24341, Republic of Korea; Department of Environmental Engineering, College of Engineering, Kangwon National University, Kangwondaehak-gil, 1, Chuncheon-si, Gangwon-do, 24341, Republic of Korea. Electronic address:

Published: August 2021

AI Article Synopsis

  • The study investigates the adsorption effectiveness of radioactive barium, cobalt, and strontium ions using two types of spent coffee waste biochars: pristine (SCWB-P) and chemically activated with NaOH (SCWB-A), finding SCWB-A to be significantly more efficient.
  • Results show that SCWB-A achieved removal efficiencies ranging from 76.6-97.3%, compared to 45.6-75.2% for SCWB-P, with the adsorption order being Ba(II) > Sr(II) > Co(II), influenced by the presence of oxygen-containing functional groups.
  • The adsorption mechanisms shifted from physisorption in SCWB-P to chemisorption in SCWB-A due to alkaline treatment

Article Abstract

The single adsorption of radioactive barium (Ba(II)), cobalt (Co(II)), and strontium (Sr(II)) ions using pristine (SCWB-P) and chemically activated spent coffee waste biochars with NaOH (SCWB-A) were thoroughly explored in order to provide deeper insights into the changes in their adsorption mechanisms through alkaline chemical activation. The greater removal efficiencies of SCWB-A (76.6-97.3%) than SCWB-P (45.6-75.2%) and the consistency between the adsorptive removal patterns (Ba(II) > Sr(II) > Co(II)) and oxygen bond dissociation enthalpies (BaO (562 kJ/mol) > SrO (426 kJ/mol) > CoO (397 kJ/mol)) of radioactive species supported the assumption that the adsorption removal of radioactive species with spent coffee waste biochars highly depended on the abundances of O-containing functional groups. The calculated R values of the pseudo-first-order (SCWB-P = 0.998-0.999; SCWB-A = 0.850-0.921) and pseudo-second-order kinetic models (SCWB-P = 0.988-0.998; SCWB-A = 0.935-0.966) are evident that the physisorption mainly controlled the adsorption of radioactive species toward SCWB-P and the chemisorption played a crucial role in their adsorptive removal with SCWB-A. From the calculated intra-particle diffusion, isotherm, thermodynamic parameters, it can be concluded that the intra-particle diffusion and monolayer adsorption primarily governed the adsorption of radioactive species using SCWB-P and SCWB-A, and their adsorption processes occurred spontaneously and endothermically. The dominant adsorption mechanism of spent coffee waste biochars was changed from physisorption (ΔH° of SCWB-P = 21.6-29.8 kJ/mol) to chemisorption (ΔH° of SCWB-A = 42.4-81.3 kJ/mol) through alkaline chemical activation. The distinctive M-OH peak in the O1s XPS spectra of SCWB-A directly corresponding to the decrease in the abundances of O-containing functional groups confirms again that the enrichment of O-containing functional groups markedly facilitated the adsorption removal of radioactive species by chemisorption occurred at the inner and outer surfaces of spent coffee waste biochars.

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Source
http://dx.doi.org/10.1016/j.envres.2021.111346DOI Listing

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