2022
DOI: 10.1039/d2gc01714h
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Efficient hydrodeoxygenation of guaiacol to phenol over Ru/Ti–SiO2 catalysts: the significance of defect-rich TiOx species

Abstract: Under relatively mild conditions (240 °C and 0.4 MPa H2), Ru/Ti–SiO2 exhibited higher activity for C–O bond cleavage compared with both Ru/SiO2 and Ru/TiO2 catalysts, and achieved high guaiacol conversion (83.6%) and phenol selectivity (70.4%).

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Cited by 32 publications
(12 citation statements)
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“…[8,[14][15][16][17][18] It is generally believed that the interfacial perimeter site between metal and oxide plays a crucial role in such improved performance. [17,[19][20][21][22][23][24][25][26][27] Newman et al reported higher benzene selectivity during HDO of phenol on Ru/TiO 2 catalysts with small Ru size (1.5 nm) than large Ru size (33 nm), and ascribed this difference to the increased Ru-TiO 2 interfacial perimeter sites for smaller Ru size. [27] Lately, direct correlation between the deoxygenation activity and interfacial perimeter site was reported on Pt/Nb 2 O 5 and Ru/TiO 2 catalysts by assuming that the number of perimeter site is related with the metal particle size.…”
Section: Importance Of Perimeter Site At Metal/oxide Interface For Hdomentioning
confidence: 99%
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“…[8,[14][15][16][17][18] It is generally believed that the interfacial perimeter site between metal and oxide plays a crucial role in such improved performance. [17,[19][20][21][22][23][24][25][26][27] Newman et al reported higher benzene selectivity during HDO of phenol on Ru/TiO 2 catalysts with small Ru size (1.5 nm) than large Ru size (33 nm), and ascribed this difference to the increased Ru-TiO 2 interfacial perimeter sites for smaller Ru size. [27] Lately, direct correlation between the deoxygenation activity and interfacial perimeter site was reported on Pt/Nb 2 O 5 and Ru/TiO 2 catalysts by assuming that the number of perimeter site is related with the metal particle size.…”
Section: Importance Of Perimeter Site At Metal/oxide Interface For Hdomentioning
confidence: 99%
“…Combination of transition metal and reducible (oxophilic) metal oxide (for example, TiO 2 ) provides both hydrogenation and deoxygenation functionalities, and has shown higher activity and selectivity of DDO toward aromatics relative to metal on an inert support of SiO 2 [8,14–18] . It is generally believed that the interfacial perimeter site between metal and oxide plays a crucial role in such improved performance [17,19–27] . Newman et al.…”
Section: Introductionmentioning
confidence: 99%
“…Typical temperatures are between 300 and 400 °C, with hydrogen pressures between 1 and 65 bar. [48][49][50][51][52] Mo based catalysts, in the form of oxides, phosphides, nitrides, and carbides, have been widely used for the catalytic demethoxylation reactions at 300-450 °C under 5-50 bar H 2 . [53][54][55][56][57][58][59] The MoN-A catalyst presented both high conversion (95%) and high selectivity (90%).…”
Section: Hydrodeoxygenation Of Other Lignin-derived Phenolic Monomersmentioning
confidence: 99%
“…49,51,52 The use of precious metal catalysts, such as Ru/TiO 2 and Au/TiO 2 , has resulted in high guaiacol conversion (>80%) but relatively poor selectivity (70.4% and 49.6%) at 240-300 °C under 4-65 bar H 2 . 48,50 Compared with these systems, our system is the only one operating under "H 2free" conditions. In another case, despite Ru/C and Ni/CeO 2 -C being employed in the "H 2 -free" HDO of guaiacol, the yield of the target product catechol was extremely low (below 7%) at a higher temperature of 250 °C.…”
Section: Hydrodeoxygenation Of Other Lignin-derived Phenolic Monomersmentioning
confidence: 99%
“…Compared with the petroleum-based polymer as a precursor, the high value-added conversion of lignin can not only effectively improve the profits of the paper and biorefining industry but also effectively reduce costs and improve the renewability in the CNF field. However, due to significant differences in the intrinsic chemical structure of lignin compared to that of other petroleum-based materials, the direct introduction of lignin through physical blending often seriously affects material properties during the preparation of high-value materials. Therefore, many strategies have been developed to chemically modify lignin macromolecules to meet the requirements of the corresponding high-value materials. In our previous study, for the preparation of lignin-based hybrid electrodes, polyaniline segments were grafted onto lignin macromolecules, which could effectively reduce the phase separation between lignin macromolecules and polyaniline segments. The obtained polyaniline-/biomass-based CNFs exhibit the complete fibrous micromorphologies, large specific surface area, and excellent electrochemical energy storage performances .…”
Section: Introductionmentioning
confidence: 99%