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Photoelectrochemical synthesis of chloroprocaine from procaine coupled with hydrogen generation
AIChE Journal ( IF 3.5 ) Pub Date : 2024-08-22 , DOI: 10.1002/aic.18591
Wangsong Chen 1 , Nenghui Pan 1 , Lan Luo 1 , Yucong Miao 1 , Shanshan Zhang 1 , Zhiyuan Zhang 2 , Ruikang Zhang 2, 3 , Zhenhua Li 1, 2 , Mingfei Shao 1, 2
Affiliation  

Chloroprocaine is favored in anesthesia for its effectiveness and safety but is produced through complex, environmentally harmful processes. There is a growing interest in developing greener, more cost-effective methods for producing chloroprocaine. Here, we establish a green and cost-effective photoelectrochemical (PEC) approach for synthesizing chloroprocaine from procaine using a WO3 photoanode with oxygen vacancies. Achieving a high yield of 18.8 μmol cm−2 h−1 with selectivity of 92% and FE of 99%, this method leverages a free radical chain mechanism initiated by Cl· radicals formed over the WO3. The incorporation of oxygen vacancies enhances light absorption and charge separation, facilitating Cl· and Cl2 generation critical for its synthesis. We successfully produced 37.4 mg of chloroprocaine and 5.4 mL of hydrogen using a self-powered PEC device, demonstrating the method effectiveness and environmental friendliness for chloroprocaine synthesis and hydrogen production.

中文翻译:


普鲁卡因光电化学合成氯普鲁卡因耦合制氢



氯普鲁卡因因其有效性和安全性而在麻醉中受到青睐,但其生产过程复杂且对环境有害。人们对开发更环保、更具成本效益的氯普鲁卡因生产方法越来越感兴趣。在这里,我们建立了一种绿色且经济高效的光电化学(PEC)方法,使用具有氧空位的WO 3光阳极从普鲁卡因合成氯普鲁卡因。该方法利用由WO 3上形成的Cl·自由基引发的自由基链机制,实现了18.8 μmol cm -2 h -1的高产率,选择性为92%,FE为99%。氧空位的结合增强了光吸收和电荷分离,促进了对其合成至关重要的Cl·和Cl 2的生成。我们利用自供电PEC装置成功生产了37.4 mg氯普鲁卡因和5.4 mL氢气,证明了氯普鲁卡因合成和制氢方法的有效性和环境友好性。
更新日期:2024-08-23
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