Zhao Heng-Fan, Yue Yu-Ting, Fan Yi-Lin, Wang Ji-Xiang, Li Wen-Hui, Wei Feng, Liu Min, Yu Yan-Hua, Lu Wang-Ting, Zhang Geng
State Key Laboratory of Precision Blasting, Jianghan University, 430056, Wuhan, P. R. China.
Key Laboratory of Optoelectronic Chemical Materials and Devices, Ministry of Education, Jianghan University, 430056, Wuhan, P. R. China.
ChemSusChem. 2022 Dec 7;15(23):e202201625. doi: 10.1002/cssc.202201625. Epub 2022 Nov 8.
The electrochemical transformation of biomass to high value-added products is attractive. Herein, Cu sulfide-mediated in-situ synthesis of Cu oxide was achieved for efficient electro-oxidation of biomass derived 5-hydroxymethylfurfural (HMF) to 2,5-furandicarboxylic acid (FDCA). The copper foam-supported Cu sulfide (Cu-S/CF) was in-situ converted to Cu oxide during the electro-oxidation process. The in-situ formed Cu oxide presented high HMF conversion, FDCA yield, and faradaic efficiency in 1 m KOH with HMF concentration up to 100 mm. The oxidation of HMF on Cu oxide started with the formation of high-valence Cu species with the assistance of OH , which then oxidized HMF spontaneously. An anion exchange membrane (AEM) electrolyzer with Cu-S/CF as the anode was assembled to continuously produce FDCA with H generation at the cathode. The AEM electrolyzer ran stably for 60 h with FDCA content higher than 85 % at a cell voltage between 1.50 and 1.60 V.
将生物质电化学转化为高附加值产品具有吸引力。在此,实现了硫化铜介导的氧化铜原位合成,用于将生物质衍生的5-羟甲基糠醛(HMF)高效电氧化为2,5-呋喃二甲酸(FDCA)。在电氧化过程中,泡沫铜负载的硫化铜(Cu-S/CF)原位转化为氧化铜。原位形成的氧化铜在1 m KOH中对HMF具有高转化率、FDCA产率和法拉第效率,HMF浓度高达100 mM。HMF在氧化铜上的氧化始于在OH的协助下形成高价铜物种,然后高价铜物种自发氧化HMF。组装了以Cu-S/CF为阳极的阴离子交换膜(AEM)电解槽,以在阴极产生氢气的同时连续生产FDCA。AEM电解槽在1.50至1.60 V的电池电压下稳定运行60 h,FDCA含量高于85%。