首页|NiFe-MOF和氮氧自由基协同增强甾醇电催化氧化

NiFe-MOF和氮氧自由基协同增强甾醇电催化氧化

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传统甾醇中间体氧化采用重金属铬作为氧化剂,存在毒性大和环境污染等问题.电催化氧化(ECO)以其高效、环保、可控的优点备受青睐,被认为是一种可替代传统工艺的方法.然而,目前ECO面临低电流密度和低时空产率的挑战.本研究采用一步溶剂热法在石墨毡上制备自支撑NiFe-MOF纳米片电催化剂,并耦合NiFe-MOF与氮氧自由基(4-乙酰氨-2,2,6,6-四甲基哌啶-1-氧)协同电催化策略以提高ECO性能.研究发现碱性电解液可重构NiFe-MOF催化剂,从而提高催化活性.此外,连续流动强化传质,成功实现以100 mA·cm-2的大电流密度对19-羟基-4-雄甾烯-3,17-二酮(1a)的选择性电催化氧化,且选择性高达98%,时空产率可达15.88 kg·m-3·h-1,是间歇电反应器的35倍.寿命测试发现经10次循环反应后,NiFe-MOF/ACT协同体系对ECO仍具有较高的转化率.通过增大NiFe-MOF面积,将其组装至连续流动式电反应器并进行ECO恒电流电解,可达到12.99 kg·m-3·h-1的时空产率.该工作提出一种NiFe-MOF/ACT协同电催化氧化策略,为实现甾醇选择性氧化提供新的见解.
Enhanced Electrocatalytic Oxidation of Sterols using the Synergistic Effect of NiFe-MOF and Aminoxyl Radicals
Conventional oxidation methods of sterol intermediates using the heavy metal chromium as an oxidant has critical drawbacks,such as high toxicity and environmental pollution.Electrocatalytic oxidation(ECO),on the other hand,is considered a promising alternative to conventional processes owing to its high efficiency,eco-friendliness,and controllability.However,ECO currently faces two major challenges:low current densities and reduced space-time yields.In this study,a single-step solvothermal method was employed to synthesize self-supported nickel-iron metal-organic framework(NiFe-MOF)nanosheet electrocatalysts on graphite felt.Various analytical techniques were employed to comprehensively characterize the synthesized NiFe-MOF,including scanning electron microscopy(SEM),X-ray photoelectron spectroscopy(XPS),X-ray diffraction(XRD),Raman spectroscopy,and Brunauer-Emmett-Teller(BET)analysis Furthermore,we implemented a synergistic electrocatalytic strategy by combining the NiFe-MOF catalyst with aminoxyl radicals,i.e.,4-acetamido-2,2,6,6-tetramethyl-1-piperidine-N-oxyl(ACT),to enhance the performance of the ECO reaction.According to the results of structural characterization,the synthesized NiFe-MOF exhibited an amorphous nanosheet structure with a high specific surface area and microporosity.Moreover,we successfully achieved continuous flow with enhanced mass transfer during the electrocatalytic oxidation of 19-hydroxy-4-androstene-3,17-dione(1a)at a current density of 100 mA·cm-2.The optimal reaction conditions for the ECO reaction were as follows:100 mmol·L-1 concentration of 1a,10%(molar fraction)of ACT,a 1 mol·L-1 Na2CO3/acetonitrile electrolyte(6:4),room temperature,pH 12.5,and a flow rate of 225 mL·min-1.Under these conditions,the conversion and selectivity of the reaction reached outstanding levels of 99 and 98%,respectively.Moreover,the space-time yield was calculated to be as high as 15.88 kg·m-3·h-1,with a remarkable 35-fold increase compared to that achieved in a batch reactor.The NiFe-MOF/ACT synergistic system demonstrated a high conversion rate for ECO even after 10 reaction cycles.To assess the system's efficacy in converting other sterols,we conducted an analysis of substrate expansion,which yielded conversion rates exceeding 95%.The SEM,TEM,and XPS results of the catalyst obtained before and after the reaction indicated that the alkaline electrolyte could effectively reconstitute the NiFe-MOF structure,leading to a significant improvement in its performance.By leveraging a ten-fold increased surface area of the NiFe-MOF and constructing a continuous flow electroreactor for ECO with a constant current,we achieved a remarkable space-time yield of 12.99 kg·m-3·h-1.Thus,we developed a synergistic electrocatalytic oxidation strategy based on NiFe-MOF/ACT,and this study not only provides valuable insights for realizing the selective oxidation of sterols but also contributes to the advancement of sustainable and efficient chemical processes.

SterolElectrocatalytic oxidationMetal-organic frameworksAminoxyl radicalSynergistic effect

许银洁、李随勤、刘力豪、贺佳辉、李凯、王梦欣、赵舒影、李纯、张峥斌、钟兴、王建国

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浙江工业大学化工学院工业催化研究所,绿色化学合成技术国家重点实验室,杭州 310032

浙江仙居君业药业有限公司研发部,浙江 台州 317300

甾醇 电催化氧化 金属有机框架 氮氧自由基 协同作用

国家重点研发计划国家重点研发计划浙江省自然科学基金国家自然科学基金国家自然科学基金国家自然科学基金国家自然科学基金

2022YFA15042002021YFA1500903LR22B06000322078293216256049193430222141001

2024

物理化学学报
中国化学会

物理化学学报

CSTPCD北大核心
影响因子:0.951
ISSN:1000-6818
年,卷(期):2024.40(3)