Conversion of acidified lignin containing sulfur discharged from a biorefinery process into neutralized biochar: Characterization and metal adsorption
- Authors
- Lee, Jeong-Min; Kim, Hae-Been; Wang, Jim J.; Zhou, Baoyue; Seo, Dong-Cheol; Park, Jong-Hwan
- Issue Date
- Dec-2024
- Publisher
- Elsevier B.V.
- Keywords
- Carbon negative; Industrial waste; Isotherm model; Kinetic; Lead; Recycling
- Citation
- Science of the Total Environment, v.954
- Indexed
- SCIE
SCOPUS
- Journal Title
- Science of the Total Environment
- Volume
- 954
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/74210
- DOI
- 10.1016/j.scitotenv.2024.176438
- ISSN
- 0048-9697
1879-1026
- Abstract
- The objectives of this study were to produce biochars using sulfur-rich acidified lignin discharged from a biorefinery process and to evaluate their physicochemical properties and Pb adsorption capacity. As the pyrolysis temperature increased, the lignin acidified by the desulfurization process was converted to neutralized biochar (LBC), which exhibited high carbon content and stability. The carbon content of biochar manufactured at a pyrolysis temperature of 600 °C or higher was over 90 % and showed no significant difference, and their surface structures were found to be different, as revealed through XRD and FTIR analyses. The adsorption capacity of Pb by LBC increased with increasing pyrolysis temperature, and their adsorption capacity was well described by the pseudo-second-order model and the Langmuir isotherm adsorption model. In particular, the internal diffusion effect on the adsorption capacity of Pb was greater for LBC900 than for LBC600. In complex heavy metal solutions, LBC selectively exhibited high affinity for Pb, while the adsorption capacity of other metals was significantly reduced. The adsorption mechanism of Pb by LBC was verified through various analytical methods, and these results demonstrated that the adsorption of Pb by LBC was influenced by functional groups existing on the surface and inside of LBC and by some cation exchange. © 2024 Elsevier B.V.
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