Flow-Through Electrochemical Membrane Reactor with a Self-Supported Carbon Membrane Electrode for Highly Efficient Synthesis of Hydrogen Peroxide

电合成 材料科学 碳化 电化学 膜反应器 化学工程 阴极 碳纤维 电极 过氧化氢 试剂 膜 有机化学 复合材料 化学 扫描电子显微镜 生物化学 物理化学 复合数 工程类
作者
Zishang Chen,Hong Wang,Xiaohua Ma,Xiaoping Chen,Shuanglin Gui,Jianxin Li
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:15 (36): 42460-42469 被引量:22
标识
DOI:10.1021/acsami.3c06307
摘要

In situ electroreduction of O 2 to H 2 O 2 by using electrons as reagents is known as a green process, which is highly desirable for environmental remediation and chemical industries. However, the development of a cost-effective electrode with superior H 2 O 2 synthesis rate and stability is challenging. A self-supported carbon membrane (CM) was prepared in this study from activated carbon and phenolic resin by carbonization under a H 2 atmosphere. It was employed as the cathode to build a flow-through electrochemical membrane reactor (FT-ECMR) for electrosynthesis of H 2 O 2 . The results showed that the CM had a small pore size (34 nm), a high porosity (42.3%), and a high surface area (450.7 m 2 g –1 ). In contrast to most of the state-of-the-art self-supported carbon electrode reported in the previous works, the FT-ECMR exhibited a high concentration of continuous and stable H 2 O 2 electrosynthesis (1042 mg L –1 ) as well as a H 2 O 2 synthesis rate of 5.21 mg h –1 cm –2 . It had also demonstrated a high oxygen conversion (0.37%) and current efficiency (88%). The outstanding performance of the FT-ECMR for H 2 O 2 synthesis was attributed to the enhanced mass transfer of the reactor, the existence of a relatively high surface area of CM, and the abundant disordered carbon structures (sp 3 -C, defects, and edges). In conclusion, our work highlighted using the FT-ECMR with the CM to synthesize H 2 O 2 efficiently and cost-effectively.
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