Published August 2021 | Version v1
Journal article

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

  • 1. Department of Integrated Energy and Infra system, Kangwon National University, Kangwondaehak-gil, 1, Chuncheon-si, Gangwon-do, 24341 (Korea, Republic of)
  • 2. Department of Environmental Engineering, College of Engineering, Kangwon National University, Kangwondaehak-gil, 1, Chuncheon-si, Gangwon-do, 24341 (Korea, Republic of)
  • 3. School of Urban and Environmental Engineering, Ulsan National Institute of Science and Technology (UNIST), 50 UNIST-gil, Eonyang-eup, Ulju-gun, Ulsan, 689-798 (Korea, Republic of)
  • 4. Korea Hydro and Nuclear Power (KHNP) Central Research Institute, 50, 1312-gil, Yuseong-daero, Yuseong-gu, Daejeon, 34101 (Korea, Republic of)
  • 5. Department of Civil and Environmental Engineering, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul (Korea, Republic of)
  • 6. Key Laboratory of Urban Stormwater System and Water Environment, Ministry of Education, Beijing University of Civil Engineering and Architecture, Beijing, 100044 (China)

Description

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 R2 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.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.envres.2021.111346

Additional details

Identifiers

DOI
10.1016/j.envres.2021.111346;
PII
S001393512100640X;

Publishing Information

Journal Title
Environmental Research
Journal Volume
199
Journal Page Range
vp.
ISSN
0013-9351
CODEN
ENVRAL

Optional Information

Copyright
Copyright (c) 2021 Elsevier Inc. All rights reserved.