方波电位在钯电极电还原乙醇胺中co2为氨基甲酸乙酯中的应用

IF 0.5 Q4 EDUCATION & EDUCATIONAL RESEARCH Rasayan Journal of Chemistry Pub Date : 2023-01-01 DOI:10.31788/rjc.2023.1628290
A.K. Alkhawaldeh, A. Al-Dhuraibi
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引用次数: 0

摘要

研究了0.1 M乙醇胺(EA)水溶液中CO2在钯金属电极上的电化学还原反应,以合成氨基甲酸乙酯(CH3CH2OC(O)NH2)。应用方波电位制度的二氧化碳(EA)被还原为有机产品。通过方波电位谱确定了CO2电催化还原的最佳条件,电势值为- 1.0 ~ 0.4 V,振幅为1.4 V,反应时间为4小时,频率为100 Hz。我们在碱性环境中进行了不同pH值和不同电压的反应,以确保生产氨基甲酸乙酯的最佳条件。钯电极对有机化合物具有较高的CO2电还原活性。采用循环伏安法、核磁共振、紫外光谱、红外光谱、热重分析、质谱等方法对有机产物进行了分析。结果表明:0.1 M乙醇胺中co2饱和还原为氨基甲酸乙酯C2H5OCONH2。在乙醇胺中饱和co2电转化为氨基甲酸乙酯的法拉第效率和电流密度分别为93%和71 mA cm−2
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APPLICATION OF SQUARE WAVE POTENTIAL REGIME TO ELECTRO REDUCTION OF CO2 IN ETHANOLAMINE INTO ETHYL CARBAMATE BY PALLADIUM ELECTRODE
Electrochemical reduction of the CO2 present in 0.1 M Ethanolamine (EA) aqueous solution at Palladium metal electrodes for the synthesis of ethyl carbamate (CH3CH2OC(O)NH2) is investigated. The application square wave potential regime of the carbon dioxide in (EA) to be reduced to an organic product. In addition to identifying optimal conditions for CO2 electrocatalysis reduction by the square wave potential regime, the potential value was between - 1.0 to 0.4 V with 1.4 V amplitude, the time of reaction was 4 hours and the frequency was 100 Hz. We have carried out reactions at various pH levels and different voltages in an alkaline environment to ensure optimal conditions for the production of ethyl carbamate. The palladium catalysts electrode has demonstrated high CO2 electro-reduction activity to the organic compound. The organic product was analyzed by cyclic voltammetry, NMR, UV spectrometry, FT-IR spectroscopy, TGA, and MS. The results suggest the reduction of CO2-saturated in 0.1 M ethanolamine to ethyl carbamate, C2H5OCONH2. The Faradaic Efficiency and current density of electro-convert CO2-saturated in ethanolamine to ethyl carbamate are 93% and 71 mA cm−2, respectively
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来源期刊
Rasayan Journal of Chemistry
Rasayan Journal of Chemistry Energy-Energy (all)
CiteScore
1.90
自引率
0.00%
发文量
196
期刊介绍: RASĀYAN Journal of Chemistry [RJC] signifies a confluence of diverse streams of chemistry to stir up the cerebral powers of its contributors and readers. By introducing the journal by this name, we humbly intent to provide an open platform to all researchers, academicians and readers to showcase their ideas and research findings among the people of their own fraternity and to share their vast repository of knowledge and information. The journal seeks to embody the spirit of enquiry and innovation to augment the richness of existing chemistry literature and theories. We also aim towards making this journal an unparalleled reservoir of information and in process aspire to inculcate and expand the research aptitude.
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