Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/40214
Title: Demineralization of common ivy-derived biomass and biochar and its effect on the resulting activated carbon properties
Authors: VERCRUYSSE, Willem 
Gomes, Caio Laurino
BLEUS, Dries 
PAPPA, Michaela 
JOOS, Bjorn 
HARDY, An 
MARCHAL, Wouter 
VANDAMME, Dries 
Issue Date: 2023
Publisher: 
Source: SEPARATION AND PURIFICATION TECHNOLOGY, 319 (Art N° 124023)
Abstract: Biomass waste often contains high amounts of inorganic impurities, which is a limitation for developing high-quality bioproducts, e.g., high-purity activated carbons (ACs). Otherwise, these would be applicable to purify polluted water and air streams. Conventionally, AC’s are purified with non-sustainable and corrosive inorganic acids. This study illustrates the successful removal of the impurities from common ivy, Hedera helix L., through treatment with a natural deep eutectic solvent (NADES), namely choline chloride-malic acid (CCl:MA, 1:1 M). The demineralization efficiency is benchmarked against H2O and dilute hydrochloric acid (HCl). Moreover, the importance of the process sequence, pre- or post- pyrolysis demineralization, for AC-production was investigated. The three solvents showed different biomass (pre-pyrolysis) demineralization efficiencies, they were ranked, from best to worst, as follows: HCl > CCl:MA > H2O. However, demineralizing the biomass after pyrolysis yielded highly porous ACs, with a good mix of meso-and micropores. In this case, no differences in removal performance could be observed between HCl and CCl:MA. Lastly, the ACs phosphate adsorption capacity was highest after demineralizing biomass with either H2O or CCl:MA. Ultimately, this investigation demonstrated CCl:MA’s potential as a green demineralization agent to treat metal-contaminated biomass in future bio-refinery processes.
Keywords: Common Ivy;Demineralization;Biochar;Natural deep-eutectic solvents;Activated carbon
Document URI: http://hdl.handle.net/1942/40214
ISSN: 1383-5866
e-ISSN: 1873-3794
DOI: 10.1016/j.seppur.2023.124023
ISI #: 001012881500001
Rights: Elsevier
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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