Yi-ping HAN , Peng LUO , Chen-xin CAI , Lei XIE , Tian-hong LU
{"title":"电位固定型电化学传感器中氨在Ir阳极上的电化学氧化","authors":"Yi-ping HAN , Peng LUO , Chen-xin CAI , Lei XIE , Tian-hong LU","doi":"10.1016/S1005-9040(09)60027-1","DOIUrl":null,"url":null,"abstract":"<div><p>Ir catalyst possesses a good electrocatalytic activity and selectivity for the oxidation of NH<sub>3</sub> and/or NH<sub>4</sub>OH at Ir anode in the potential fixed electrochemical sensor with the neutral solution. Owing to the same electrochemical behavior of NH<sub>3</sub> and NH<sub>4</sub>OH in a NaClO<sub>4</sub> solution, NH<sub>4</sub>OH can be used instead of NH<sub>3</sub> for the experimental convenience. It was found that the potential of the oxidation peak of NH<sub>4</sub>OH at the Ir/GC electrode in NaClO<sub>4</sub> solutions is at about 0.85 V, and the current density of the oxidation peak of NH<sub>4</sub>OH is linearly proportional to the concentration of NH<sub>4</sub>OH. The electrocatalytic oxidation of NH<sub>4</sub>OH is diffusion-controlled. Especially, Ir has no electrocatalytic activity for the CO oxidation, illustrating that CO does not interfere in the measurement of NH<sub>4</sub>OH and the potential fixed electrochemical NH<sub>3</sub> sensor with the neutral solution, and the anodic Ir catalyst possesses a good selectivity. Therefore, Ir may have practical application in the potential fixed electrochemical NH<sub>3</sub> sensor with the neutral solution.</p></div>","PeriodicalId":9785,"journal":{"name":"Chemical Research in Chinese Universities","volume":"24 6","pages":"Pages 782-785"},"PeriodicalIF":3.1000,"publicationDate":"2008-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1005-9040(09)60027-1","citationCount":"3","resultStr":"{\"title\":\"Electrochemical Oxidation of Ammonia on Ir Anode in Potential Fixed Electrochemical Sensor\",\"authors\":\"Yi-ping HAN , Peng LUO , Chen-xin CAI , Lei XIE , Tian-hong LU\",\"doi\":\"10.1016/S1005-9040(09)60027-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Ir catalyst possesses a good electrocatalytic activity and selectivity for the oxidation of NH<sub>3</sub> and/or NH<sub>4</sub>OH at Ir anode in the potential fixed electrochemical sensor with the neutral solution. Owing to the same electrochemical behavior of NH<sub>3</sub> and NH<sub>4</sub>OH in a NaClO<sub>4</sub> solution, NH<sub>4</sub>OH can be used instead of NH<sub>3</sub> for the experimental convenience. It was found that the potential of the oxidation peak of NH<sub>4</sub>OH at the Ir/GC electrode in NaClO<sub>4</sub> solutions is at about 0.85 V, and the current density of the oxidation peak of NH<sub>4</sub>OH is linearly proportional to the concentration of NH<sub>4</sub>OH. The electrocatalytic oxidation of NH<sub>4</sub>OH is diffusion-controlled. Especially, Ir has no electrocatalytic activity for the CO oxidation, illustrating that CO does not interfere in the measurement of NH<sub>4</sub>OH and the potential fixed electrochemical NH<sub>3</sub> sensor with the neutral solution, and the anodic Ir catalyst possesses a good selectivity. Therefore, Ir may have practical application in the potential fixed electrochemical NH<sub>3</sub> sensor with the neutral solution.</p></div>\",\"PeriodicalId\":9785,\"journal\":{\"name\":\"Chemical Research in Chinese Universities\",\"volume\":\"24 6\",\"pages\":\"Pages 782-785\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2008-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1005-9040(09)60027-1\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Research in Chinese Universities\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1005904009600271\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Research in Chinese Universities","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1005904009600271","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Electrochemical Oxidation of Ammonia on Ir Anode in Potential Fixed Electrochemical Sensor
Ir catalyst possesses a good electrocatalytic activity and selectivity for the oxidation of NH3 and/or NH4OH at Ir anode in the potential fixed electrochemical sensor with the neutral solution. Owing to the same electrochemical behavior of NH3 and NH4OH in a NaClO4 solution, NH4OH can be used instead of NH3 for the experimental convenience. It was found that the potential of the oxidation peak of NH4OH at the Ir/GC electrode in NaClO4 solutions is at about 0.85 V, and the current density of the oxidation peak of NH4OH is linearly proportional to the concentration of NH4OH. The electrocatalytic oxidation of NH4OH is diffusion-controlled. Especially, Ir has no electrocatalytic activity for the CO oxidation, illustrating that CO does not interfere in the measurement of NH4OH and the potential fixed electrochemical NH3 sensor with the neutral solution, and the anodic Ir catalyst possesses a good selectivity. Therefore, Ir may have practical application in the potential fixed electrochemical NH3 sensor with the neutral solution.
期刊介绍:
The journal publishes research articles, letters/communications and reviews written by faculty members, researchers and postgraduates in universities, colleges and research institutes all over China and overseas. It reports the latest and most creative results of important fundamental research in all aspects of chemistry and of developments with significant consequences across subdisciplines.
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