Synthesis of ultrafine Mo2N particles supported on N doped carbon material for guaiacol hydrodeoxygenation
A series of Mo2N particles supported on nitrogen-doped carbon (Mo2N@NC) catalysts for guaiacol hydrodeoxygenation were synthesized in situ through a one-step method employing dopamine as C and N resources and ammonium molybdate as Mo resource, respectively. During synthesis, molybdate ions are adsor...
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Veröffentlicht in: | Biomass & bioenergy 2024-08, Vol.187, p.107289, Article 107289 |
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Sprache: | eng |
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Zusammenfassung: | A series of Mo2N particles supported on nitrogen-doped carbon (Mo2N@NC) catalysts for guaiacol hydrodeoxygenation were synthesized in situ through a one-step method employing dopamine as C and N resources and ammonium molybdate as Mo resource, respectively. During synthesis, molybdate ions are adsorbed on dopamine because of a complexation between them; then dopamine/molybdate ions/TMB/F127 nanoemulsions are formed. After polymerization, growth, drying, and carbonization, Mo2N particles supported on nitrogen-doped carbon catalysts are obtained. Because of the interaction between Mo and N, Mo2N particles are anchored onto the support, preventing the aggregation of Mo2N during carbonization. As a result, ultrafine Mo2N particles with a size of 1.0–1.3 nm are highly dispersed on Mo2N@NC catalysts. The guaiacol hydrodeoxygenation for these Mo2N@NC catalysts was performed at 280–380 °C, a H2 flow rate of 80 mL/min and different pressures and weight hourly space velocities. Among them, Mo2N@NC with a Mo2N loading of 40 % presents the highest guaiacol conversion (99.9 %) and aromatic hydrocarbon selectivity (80.2 %), which is also better than Mo2N/C with a Mo2N loading of 40 % prepared by the wet impregnation method.
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•Mo2N particles supported on N-doped carbon catalysts were synthesized.•The above synthesized Mo2N@NC possessed ultrafine Mo2N particles.•40-Mo2N@NC had the most active sites for guaiacol hydrodeoxygenation.•40-Mo2N@NC showed the highest aromatic hydrocarbon selectivity in guaiacol HDO. |
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ISSN: | 0961-9534 1873-2909 |
DOI: | 10.1016/j.biombioe.2024.107289 |