Abstrakti
Hardwood spent mushroom substrate was employed as a carbon precursor to prepare activated biochars using phosphoric acid (H3PO4) as chemical activator. The activation process was carried out using an impregnation ratio of 1 precursor:2 H3PO4; pyrolysis temperatures of 700, 800, and 900 °C; heating rate of 10 °C min−1; and treatment time of 1 h. The specific surface area (SSA) of the biochars reached 975, 1031, and 1215 m2 g−1 for the samples pyrolyzed at 700, 800, and 900 °C, respectively. The percentage of mesopores in their structures was 75.4%, 78.5%, and 82.3% for the samples pyrolyzed at 700, 800, and 900 °C, respectively. Chemical characterization of the biochars indicated disordered carbon structures with the presence of oxygen and phosphorous functional groups on their surfaces. The biochars were successfully tested to adsorb acetaminophen and treat two simulated pharmaceutical effluents composed of organic and inorganic compounds. The kinetic data from adsorption of acetaminophen were fitted to the Avrami fractional-order model, and the equilibrium data was well represented by the Liu isotherm model, attaining a maximum adsorption capacity of 236.8 mg g−1 for the biochar produced at 900 °C. The adsorption process suggests that the pore-filling mechanism mainly dominates the acetaminophen removal, although van der Walls forces are also involved. The biochar produced at 900 °C removed up to 84.7% of the contaminants in the simulated effluents. Regeneration tests using 0.1 M NaOH + 20% EtOH as eluent showed that the biochars could be reused; however, the adsorption capacity was reduced by approximately 50% after three adsorption–desorption cycles.
| Alkuperäiskieli | Englanti |
|---|---|
| Sivut | 2293-2309 |
| Sivumäärä | 17 |
| Julkaisu | Biomass Conversion and Biorefinery |
| Vuosikerta | 14 |
| Numero | 2 |
| DOI - pysyväislinkit | |
| Tila | Julkaistu - tammik. 2024 |
| OKM-julkaisutyyppi | A1 Julkaistu artikkeli, soviteltu |
Rahoitus
Open access funding provided by Swedish University of Agricultural Sciences. This research was funded by the Re:source program (P42481) and BioInnovation (2017–02705), co-financed by the Swedish State Innovation Department (VINNOVA), the Swedish Energy Agency, and the Swedish Research Council FORMAS (2021–00877). We thank Bio4Energy, a Strategic Research Environment appointed by the Swedish government, as well as the Swedish University of Agricultural Sciences for supporting this work. The Umeå Core Facility for Electron Microscopy (UCEM-NMI node) and the Vibrational Spectroscopy Core Facility (ViSp) at the Chemical Biological Centre (KBC), Umeå University, are gratefully acknowledged. The Wallenberg Wood Science Center (WWSC) is gratefully acknowledged. This work is also a part of the Johan Gadolin Process Chemistry Centre at Åbo Akademi University. The authors want to thank Alexandr Talyzin, Department of Physics, Umeå University, for the valuable comments on the manuscript. We thank Bio4Energy, a Strategic Research Environment appointed by the Swedish government, as well as the Swedish University of Agricultural Sciences for supporting this work. The Umeå Core Facility for Electron Microscopy (UCEM-NMI node) and the Vibrational Spectroscopy Core Facility (ViSp) at the Chemical Biological Centre (KBC), Umeå University, are gratefully acknowledged. The Wallenberg Wood Science Center (WWSC) is gratefully acknowledged. This work is also a part of the Johan Gadolin Process Chemistry Centre at Åbo Akademi University. The authors want to thank Alexandr Talyzin, Department of Physics, Umeå University, for the valuable comments on the manuscript.
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