ZrO2-doped Cu-Pd alloy catalyst for the direct synthesis of 2,5-dimethylfuran from cellulose in sub- and supercritical methanol

被引:2
作者
Verma, Deepak [1 ,2 ]
Insyani, Rizki [3 ]
Kurniawan, Rizky Gilang [2 ]
Jo, Heuntae [1 ]
Hakeem, Luqman [2 ]
Kim, Jaehoon [1 ,2 ,3 ]
机构
[1] Sungkyunkwan Univ, Sch Mech Engn, 2066 Seobu Ro, Suwon 16419, Gyeong Gi Do, South Korea
[2] Sungkyunkwan Univ, Sch Chem Engn, 2066 Seobu Ro, Suwon 16419, Gyeong Gi Do, South Korea
[3] Sungkyunkwan Univ, SKKU Adv Inst Nanotechnol SAINT, 2066 Seobu Ro, Suwon 16419, Gyeong Gi Do, South Korea
基金
新加坡国家研究基金会;
关键词
Cellulose; 2,5-Dimethylfuran; Direct conversion; Zirconium doping; Cu-Pd alloy; ONE-POT CONVERSION; HIGH-YIELD; FURFURYL ALCOHOL; CO2; HYDROGENATION; BIO-OIL; ACID; OXIDATION; ZIRCONIA; OXYGEN; PERFORMANCE;
D O I
10.1016/j.cej.2024.153696
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The direct conversion of cellulose to targeted chemicals remains challenging owing to its recalcitrant nature and highly oxygenated structure. Herein, we report a strategy to selectively produce 2,5-dimethylfuran (2,5-DMF) and 2,5-hexadione (2,5-HDN) directly from cellulose, with yields of 33.8% and 17.2%, respectively, over multifunctional heterogeneous ZrO2-doped bimetallic Cu-Pd nanoparticles supported on the HY(5.1) catalyst (CuPdZr/Y) under supercritical methanol (scMeOH) conditions. Acidic and metallic sites on the catalyst are involved in sequential cascade reactions, including solvolysis, dehydration, hydrogenation (HD), and hydrogenolysis (HDO). The preferential adsorption of reaction intermediates on the oxygen vacant sites of ZrOx located near the metallic sites promoted HD and HDO. H-D exchange reactions revealed that the hydroxyl hydrogens of methanol were the active hydrogen atoms participating in HD and HDO. The yields of 2,5-DMF and 2,5-HDN decreased marginally after the third run, indicating that CuPdZr/Y was highly robust under the scMeOH reaction conditions.
引用
收藏
页数:18
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