{"title":"A benzene selective electrode","authors":"L. Warner, D. Russell, J. Scaggs","doi":"10.1109/UGIM.2003.1225763","DOIUrl":null,"url":null,"abstract":"An innovative method for benzene detection has been created. Using polymer assisted molecular recognition an electrode sensitive to benzene has been developed. A functionalized form of thiophene (3-thiophenemethanol) is covalently attached to a template molecule (isophthaloyl dichloride), an analogue of benzene. The monomer-template complex (bis(thiene-3-ylmethyl) isophthalate) is immobilized onto a platinum electrode by polymerizing onto a bithiophene plated electrode via galvanometric solution polymerization. The template molecule is then removed by subjecting the electrode to an aqueous solution of NaOH at approximately pH 10 for 2-3 minutes. This removal opens a \"binding site\" for benzene. Reversible cyclic voltammetric waves show that benzene does interact with the \"binding sites\" when compared to pure thiophene and bare platinum.","PeriodicalId":356452,"journal":{"name":"Proceedings of the 15th Biennial University/Government/ Industry Microelectronics Symposium (Cat. No.03CH37488)","volume":"9 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2003-09-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Proceedings of the 15th Biennial University/Government/ Industry Microelectronics Symposium (Cat. No.03CH37488)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/UGIM.2003.1225763","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
An innovative method for benzene detection has been created. Using polymer assisted molecular recognition an electrode sensitive to benzene has been developed. A functionalized form of thiophene (3-thiophenemethanol) is covalently attached to a template molecule (isophthaloyl dichloride), an analogue of benzene. The monomer-template complex (bis(thiene-3-ylmethyl) isophthalate) is immobilized onto a platinum electrode by polymerizing onto a bithiophene plated electrode via galvanometric solution polymerization. The template molecule is then removed by subjecting the electrode to an aqueous solution of NaOH at approximately pH 10 for 2-3 minutes. This removal opens a "binding site" for benzene. Reversible cyclic voltammetric waves show that benzene does interact with the "binding sites" when compared to pure thiophene and bare platinum.