Haemoglobin immobilized on nafion modified multi-walled carbon nanotubes for O2, H2O2 and CCl3COOH sensors

被引:42
|
作者
Shie, Jan-Wei [1 ]
Yogeswaran, Umasankar [1 ]
Chen, Shen-Ming [1 ]
机构
[1] Natl Taipei Univ Technol, Dept Chem Engn & Biotechnol, Taipei 106, Taiwan
关键词
Multiwall carbon nanotubes; Modified electrodes; Electrocatalysis; Hydrogen peroxide; Trichloroacetic acid; Oxygen; PYROLYTIC-GRAPHITE ELECTRODES; DIRECT ELECTROCHEMISTRY; ASCORBIC-ACID; COMPOSITE FILMS; URIC-ACID; ELECTROCATALYSIS; PLATINUM; NANOPARTICLES; SEPARATION; REDUCTION;
D O I
10.1016/j.talanta.2008.12.063
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A conductive biocomposite film (MWCNTs-NF-Hb) containing multi-walled carbon nanotubes (MWCNTs) incorporated with entrapped haemoglobin (Hb) in nafion (NF) has been synthesized on glassy carbon electrode (GCE). gold (Au), indium tin oxide (ITO) and screen printed carbon electrode (SPCE) separately by potentiostatic methods. The presence of both MWCNTs and NF in the biocomposite film enhances the Surface coverage concentration (Gamma). and increases the electron transfer rate constant (K-s) to 132%. The biocomposite film exhibits a promising enhanced electrocatalytic activity towards the reduction of O-2, H2O2 and CCl3COOH. The cyclic voltammetry has been used for the measurement of electrocatalysis results of analytes by means of biocomposite film-modified GCEs. The MWCNTs-NF-Hb-modified GCEs' sensitivity values are higher than the Values obtained for other film modified GCEs. The surface morphology of the biocomposite films which have been deposited on ITO has been studied Using scanning electron microscopy and atomic force microscopy. The Studies have revealed that there was an incorporation of NF and immobilization of fib on MWCNTs. Finally, the flow injection analysis has been used for the amperometric studies of analytes at MWCNTs-Hb and MWCNTs-NF-Hb film modified SPCEs. The amperometric Study results have shown higher slope values for MWCNTs-NF-Hb biocomposite film. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:896 / 902
页数:7
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