Electrochemical Synthesis and Characterization of Polymers and Copolymers of 3-Hexylthiophene, 3-Methylthiophene and 3-Octylthiophene

dc.contributor.advisorYohannes, Teketel (PhD)
dc.contributor.authorAdam, Getachew
dc.date.accessioned2018-06-19T05:24:29Z
dc.date.accessioned2023-11-09T16:17:32Z
dc.date.available2018-06-19T05:24:29Z
dc.date.available2023-11-09T16:17:32Z
dc.date.issued2005-06
dc.description.abstractThe electrochemical polymerizations and characterization studies were made for the monomers 3-hexylthiophene (3HT), 3-methylthiophene (3MT) and 3-octylthiophene (3OT).The electrochemical properties of the corresponding polymers poly(3-hexylthiophene) (P3HT) , poly(3-methylthiophene) (P3MT) and poly(3-octylthiophene) (P3OT) were also studied in a monomer free LiClO4 - acetonitrile solutions. Copolymers were electrochemically synthesized from the monomers and showed intermediate electrochemical properties between their corresponding homopolymers. The first copolymer obtained was the copolymer of 3HT and 3OT (poly(3HT-co-3OT)) from 1:1.5 volume ratio of 3HT to 3OT at a potential of 1.70 V in 0.1 M LiClO4 - acetonitrile solution and the second was the copolymer of 3MT and 3OT, (poly(3MT-co-3OT)) from 1:2.5 volume ratio of 3HT to 3OT at a potential of 2.00 V in LiClO4 - acetonitrile solution. The electrocatalytic effects of the polymers and copolymers electrochemically modified on platinum disc electrode were examined using ferricyanide redox system. Among the polymers examined a copolymer of 3MT and 3OT showed the best electrocatalytic effect. Based on this result the electrocatalytic effect of this copolymer was further studied on selected environmental and biological samples. It was found that poly(3MT-co-3OT) modified platinum electrode is highly selective and sensitive towards a) detection of ferricyanide with the detection limit of 20 M, in 1 M aqueous potassium nitrate solution using cyclic voltammetry, b) simultaneous detection of the isomeric compounds hydroquinone and catechol with a detection limit of 40 M for both analytes in phosphoric acid solution pH = 0.5 using differential pulse voltammetry, c) detection of ascorbic acid with a detection limit of 80 M in phosphate buffer solution pH = 4.0 using differential pulse voltammetry, d) selective detection of catechol in the presence of the known interferance asorbic acid with a detection limit of 80 µM in phosphate buffer solution pH = 4.0 using differential pulse voltammetry. Key words; poly(3-hexylthiophene), poly(3-methylthiophene), poly(3-octylthiophene), poly(3HT-co-3OT), poly(3MT-co-3OT), Electrochemical Polymerization, Electrocatalysisen_US
dc.identifier.urihttp://etd.aau.edu.et/handle/12345678/1426
dc.language.isoenen_US
dc.publisherAddis Ababa Universtyen_US
dc.subjectpoly(3-hexylthiophene); poly(3-methylthiophene); poly(3-octylthiophene); poly(3HT-co-3OT); poly(3MT-co-3OT); Electrochemical Polymerization; Electrocatalysisen_US
dc.titleElectrochemical Synthesis and Characterization of Polymers and Copolymers of 3-Hexylthiophene, 3-Methylthiophene and 3-Octylthiopheneen_US
dc.typeThesisen_US

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