Citation:
	            
		            Di Ma,  Shenglu Lu,  Xiaohui Liu,  Yong Guo,  Yanqin Wang. Depolymerization and hydrodeoxygenation of lignin to aromatic hydrocarbons with a Ru catalyst on a variety of Nb-based supports[J]. Chinese Journal of Catalysis,
							;2019, 40(4): 609-617.
						
							doi:
								S1872-2067(19)63317-6
						
					
				
					
				
	        
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	                	Efficient conversion of lignin to aromatic hydrocarbons via depolymerization and subsequent hydrodeoxygenation is important. Previously, we found that NbOx species played a key role in the activation and cleavage of C-O bonds in lignin and its model compounds. In this study, commercial niobic acid (HY-340), niobium phosphate (NbPO-CBMM) and lab-made layered niobium oxide (Nb2O5-Layer) were chosen as supports to study the effect of Brönsted and Lewis acids on the activation of C-O bonds in lignin conversion. A variety of Ru-loaded, Nb-based catalysts with different Ru particle sizes were prepared and applied to the conversion of p-cresol. The results show that all the Ru/Nb-based catalysts produce high mole yields of C7-C9 hydrocarbons (82.3%-99.1%). What's more, Ru/Nb2O5-Layer affords the best mole yield of C7-C9 hydrocarbons and selectivity for C7-C9 aromatic hydrocarbons, of up to 99.1% and 88.0%, respectively. Moreover, it was found that Lewis acid sites play important roles in the depolymerization of enzymatic lignin into phenolic monomers and the cleavage of the C-O bond of phenols. Additionally, the electronic state and particle size of Ru are significant factors which influence the selectivity for aromatic hydrocarbons. A partial positive charge on the metallic Ru surface and a smaller Ru particle size are beneficial in improving the selectivity for aromatic hydrocarbons.
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								Keywords:
								
 - Lignin,
 - Aromatic hydrocarbons,
 - Nb-based supports,
 - Lewis acid sites,
 - Ru
 
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