Mild hydrogenolysis of lignin model compound and organosolv lignin over non-noble bimetallic Ni-Fe/TiN catalyst

被引:16
|
作者
Nguyen, Tang Son [1 ]
Le, Manh Tu [2 ]
Nguyen, Van Hieu [3 ]
机构
[1] Fac Biotechnol Chem & Environm Engn, Ho Chi Minh City, Vietnam
[2] Fac Mat Sci & Engn, Hanoi, Vietnam
[3] Phenikaa Univ, Fac Elect & Elect Engn, Hanoi 12116, Vietnam
关键词
Lignin; Hydrogenolysis; Renewable aromatics; Nickel; Catalysis; Titanium nitride; BENZYL PHENYL ETHER; C-O BOND; PHASE HYDRODEOXYGENATION; SELECTIVE CLEAVAGE; KRAFT LIGNIN; NICKEL; DEPOLYMERIZATION; FE; PD; NANOPARTICLES;
D O I
10.1016/j.biombioe.2023.106821
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Lignin is one of the most promising feedstocks for renewable aromatics production. Conversion of such feedstock into aromatics can be attained through catalytic hydrogenolysis. In this work, NixFey/TiN bimetallic catalysts were evaluated in the hydrogenolysis of both: (i) benzyl phenyl ether (BPE) as a model compound for lignin and (ii) real organosolv lignin feedstock under low temperature (150 degrees C) and low H2 pressure (12 bar). All bimetallic catalysts exhibited superior performance over single-component materials and were shown to compose of uni-formly/highly dispersed and intimately mixed Ni and Fe nanoparticles. Among bimetallic materials, Ni5Fe2/TiN possesses the highest activity in BPE hydrogenolysis, which is comparable to that of a 5% Pd/C commercial catalyst while showing significantly higher aromatic selectivity. Ni5Fe2/TiN catalyst also outperformed Pd/C in hydrogenolysis of organosolv lignin, shown by its higher oil yield, greater content of phenolic monomers, and lower content of dimers. This material exhibited good stability in BPE conversion with no noticeable deactivation over 5 recycling cycles. XANES analysis suggests the electron transfer from Ni to Fe, which explains the superior activity observed with Ni5Fe2/TiN.
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页数:13
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