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Effective Dispersion of MgO Nanostructure on Biochar Support as a Basic Catalyst for Glucose Isomerization

Authors
Chen, Season S.Cao, YangTsang, Daniel C. W.Tessonnier, Jean-PhilippeShang, JinHou, DeyiShen, ZhengtaoZhang, ShichengOk, Yong SikWu, Kevin C. -W.
Issue Date
11-5월-2020
Publisher
AMER CHEMICAL SOC
Keywords
Heterogeneous basic catalysts; Engineered biochar; Waste management; Sustainable biorefinery; Metal-biomass interaction
Citation
ACS SUSTAINABLE CHEMISTRY & ENGINEERING, v.8, no.18, pp.6990 - 7001
Indexed
SCIE
SCOPUS
Journal Title
ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume
8
Number
18
Start Page
6990
End Page
7001
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/56019
DOI
10.1021/acssuschemeng.0c00278
ISSN
2168-0485
Abstract
Glucose isomerization to fructose is one of the most important reactions in the field of biomass valorization. We demonstrate wood waste valorization with MgCl2 salt to synthesize an environment-friendly catalyst (i.e., MgO-biochar), which exhibits effective glucose-to-fructose isomerization with over 30% fructose yield and 80% selectivity at only 100 degrees C for 30 min in water as a green medium. This study highlights that one-step synthesis can effectively disperse and tether MgO nanostructures to the biochar matrix, which displays a significant reduction of Mg leaching compared to MgO-biochars produced by two-step synthesis and pure MgO. The MgCl2 acts as a porogen that facilitates the formation of a porous biochar structure and dispersion of nanostructured MgO. We identify key parameters of impregnation media (ethylene glycol, ethanol, and water) and pyrolysis conditions (600/750 degrees C in N-2/CO2 atmosphere) that are responsible for adjusting the reactivity and stability of MgO, which enable the design of more effective and recyclable biochar catalysts. Weak interactions between MgCl2 and biomass in the presence of aqueous miscible organic solvents as shape-directing agents are accountable for fast leaching of Mg from the MgO-biochar surface. The FTIR spectra confirm the existence of various coordinations on the hydroxylated surfaces of MgO-biochar surfaces. The mesoporous structures of the biochar support enhance the stability of MgO moieties as revealed by BET, XRD, and Raman analyses. Given the benefits of effective MgO dispersion on the biochar support, we can reduce the amount of MgO active species involved in each reaction run, which mitigates over-reaction compared to pure MgO catalysts and achieves high fructose yield and selectivity for three consecutive cycles.
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