Carbon nanotube modified glassy carbon electrode for electrochemical oxidation of alkylphenol ethoxylate

被引:5
|
作者
Patino, Yolanda [1 ]
Diaz, Eva [1 ]
Jesus Lobo-Castanon, Maria [2 ]
Ordonez, Salvador [1 ]
机构
[1] Univ Oviedo, Fac Chem, Dept Chem & Environm Engn, Julian Claveria S-N, E-33006 Oviedo, Spain
[2] Univ Oviedo, Fac Chem, Dept Phys & Analyt Chem, Julian Claveria S-N, E-33006 Oviedo, Spain
关键词
advanced oxidation processes (AOPs); cyclic voltammetry; emerging pollutants; endocrine disruptors; ENDOCRINE-DISRUPTING COMPOUNDS; NONYLPHENOL ETHOXYLATES; ESTROGENIC ACTIVITY; ANTIHISTAMINE DRUG; REMOVAL; WATER; DEGRADATION; ADSORPTION; BEHAVIOR; SENSOR;
D O I
10.2166/wst.2018.196
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Electrochemical oxidation of an emerging pollutant, 2-(4-methylphenoxy) ethanol (MPET), from water has been studied by cyclic voltammetry (CV). Multiwall carbon nanotubes glassy carbon electrodes (MWCNT-GCE) were used as working electrode due to their extraordinary properties. The oxidation process is irreversible, since no reduction peaks were observed in the reverse scan. The electrocatalytic effect of MWCNT was confirmed as the oxidation peak intensity increases in comparison to bare-GCE. The effect of functional groups on MWCNT was also studied by MWCNT functionalized with NH2 (MWCNT-NH2) and COOH (MWCNT-COOH) groups. The oxidation peak current decreases in the following order: MWCNT > MWCNT-NH2 > MWCNT-COOH. Taking into account the normalized peak current, MWCNT-NH2 exhibits the best results due to its strong interaction with MPET. Under optimal conditions (pH = 5.0 and volume of MWCNT = 10 mu L), degradation was studied for MWCNT-GCE and MWCNT-NH2-GCE. A complete MPET removal was observed using MWCNT-GCE after four CV cycles, for a volume/area (V/A) ratio equal to 19. In the case of MWCNT-NH2-GCE, the maximum MPET removal was close to 90% for V/A = 37, higher than that obtained for MWCNT-GCE at the same conditions (approximate to 80%). In both cases, no organic by-products were detected.
引用
收藏
页码:2436 / 2444
页数:9
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