O2-H2O2 high-efficient co-oxidation of carbohydrate biomass to formic acid via Co3O4/C nanocatalyst

被引:2
作者
Chen, Yujie [1 ,5 ]
Yang, Yang [1 ]
Liu, Xu [1 ]
Jin, Fangming [1 ,2 ,3 ,4 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Environm Sci & Engn, State Key Lab Met Matrix Composites, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Key Lab Hydrogen Sci, Shanghai 200240, Peoples R China
[3] Shanghai Jiao Tong Univ, Ctr Hydrogen Sci, Shanghai 200240, Peoples R China
[4] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
[5] Suzhou Ind Pk Inst Vocat Technol, Suzhou 215000, Peoples R China
来源
CARBON NEUTRALITY | 2024年 / 3卷 / 01期
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
Formic acid; Carbohydrate biomass; O-2-H2O2; co-oxidation; Co3O4/C; Free radical; ACETIC-ACID; CONVERSION; OXIDATION; TEMPERATURE; PYROLYSIS; STABILITY; CELLULOSE; GLUCOSE; FORMATE;
D O I
10.1007/s43979-024-00099-3
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The conversion of biomass to chemicals/fuels has emerged as a valuable solution that offers both environmental and economic benefits, with the transformation of carbohydrate into formic acid garnering escalating scholar interest. However, the relative limited efficiency of catalyzed-oxidation or expensive cost of H2O2 and alkali in wet hydrothermal oxidation impose limitations on industrialization. This paper proposed a new idea for formic acid production by O-2-H2O2 co-oxidation of carbohydrate. A two-step reaction method was developed, where the initial step is engineered to regulate the carbon chain cleavage of carbohydrates to augment the production of active intermediate. Oxygen was employed in the subsequent step as effective oxidant through free radical mechanism, resulting in a formic acid yield of 82.6%. Theoretical calculation, intermediates detection and real time EPR confirmed the reaction mechanism. Finally, the universality of the reaction was verified by using disaccharides and polysaccharides such as cellulose as substrates.
引用
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页数:12
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