TY - JOUR
T1 - Activated biochars as sustainable and effective supports for hydrogenations
AU - Taghavi, Somayeh
AU - Ghedini, Elena
AU - Peurla, Markus
AU - Cruciani, Giuseppe
AU - Menegazzo, Federica
AU - Murzin, Dmitry Yu
AU - Signoretto, Michela
N1 - Publisher Copyright:
© 2023
PY - 2023/12
Y1 - 2023/12
N2 - Activated biochars were obtained from pyrolysis and CO2-physical activation of four different biomasses including tannery shaving waste (T), vine wood waste (W), barley waste (B) and Sargassum, brown macroalgae of Venice lagoon (A). The potential of obtained carbonaceous materials as the supports of Ni,Al catalysts was investigated in levulinic acid (LA) conversion to γ-valerolactone (GVL) as a model hydrogenation reaction. Al-containing species as the Lewis acid sites for the dehydration step were incorporated to the supports using wet impregnation or precipitation. Ni as a hydrogenation active phase was added to the supports via wet impregnation. Biochar-based supports and catalysts were characterized by AAS, elemental analysis, FTIR, N2 physisorption, XRD, SEM, EDS, TEM, He-TPD, NH3-TPD and TPR techniques. The catalysts were tested for LA hydrogenation to GVL in a batch system and aqueous medium. The results showed that Ni supported on activated biochar was not active due to a lack of Lewis acid sites for dehydration. Precipitated Al-containing species on the biochar-based supports demonstrated a better catalytic performance in the reaction compared to impregnated one because of different interactions with the support and Ni species. Among different supports, the activated biochars obtained from T and W acted as the best ones. A higher catalytic efficiency was strongly influenced by the chemical (aromaticity and stability, presence of N,O-doped and functional groups), textural (the porous texture and surface area), and morphological (higher dispersion of active phases) properties of activated biochars obtained from different biomasses with different natures.
AB - Activated biochars were obtained from pyrolysis and CO2-physical activation of four different biomasses including tannery shaving waste (T), vine wood waste (W), barley waste (B) and Sargassum, brown macroalgae of Venice lagoon (A). The potential of obtained carbonaceous materials as the supports of Ni,Al catalysts was investigated in levulinic acid (LA) conversion to γ-valerolactone (GVL) as a model hydrogenation reaction. Al-containing species as the Lewis acid sites for the dehydration step were incorporated to the supports using wet impregnation or precipitation. Ni as a hydrogenation active phase was added to the supports via wet impregnation. Biochar-based supports and catalysts were characterized by AAS, elemental analysis, FTIR, N2 physisorption, XRD, SEM, EDS, TEM, He-TPD, NH3-TPD and TPR techniques. The catalysts were tested for LA hydrogenation to GVL in a batch system and aqueous medium. The results showed that Ni supported on activated biochar was not active due to a lack of Lewis acid sites for dehydration. Precipitated Al-containing species on the biochar-based supports demonstrated a better catalytic performance in the reaction compared to impregnated one because of different interactions with the support and Ni species. Among different supports, the activated biochars obtained from T and W acted as the best ones. A higher catalytic efficiency was strongly influenced by the chemical (aromaticity and stability, presence of N,O-doped and functional groups), textural (the porous texture and surface area), and morphological (higher dispersion of active phases) properties of activated biochars obtained from different biomasses with different natures.
KW - Activated biochar
KW - Aluminum
KW - Biomass pyrolysis
KW - Hydrogenation catalyst
KW - Nickel
KW - Biomass pyrolysis
KW - Hydrogenation catalyst
KW - Aluminum
KW - Nickel
KW - Activated biochar
UR - http://www.scopus.com/inward/record.url?scp=85178131682&partnerID=8YFLogxK
U2 - 10.1016/j.cartre.2023.100316
DO - 10.1016/j.cartre.2023.100316
M3 - Article
AN - SCOPUS:85178131682
SN - 2667-0569
VL - 13
JO - Carbon Trends
JF - Carbon Trends
M1 - 100316
ER -