Characterization by Electrochemical and X-ray Photoelectron Spectroscopic Measurements and Quantum Chemical Calculations of N-Containing Functional Groups Introduced onto Glassy Carbon Electrode Surfaces by Electrooxidation of a Carbamate Salt in Aqueous Solutions

Langmuir ◽  
2014 ◽  
Vol 30 (18) ◽  
pp. 5297-5305 ◽  
Author(s):  
Aiko Kanazawa ◽  
Takuro Daisaku ◽  
Takeyoshi Okajima ◽  
Shunichi Uchiyama ◽  
Susumu Kawauchi ◽  
...  
ACS Omega ◽  
2021 ◽  
Vol 6 (38) ◽  
pp. 24419-24431
Author(s):  
Nor Dyana Zakaria ◽  
Muhamad Huzaifah Omar ◽  
Najahtul Najihah Ahmad Kamal ◽  
Khairunisak Abdul Razak ◽  
Turgut Sönmez ◽  
...  

1998 ◽  
Vol 37 (11) ◽  
pp. 2633-2644 ◽  
Author(s):  
María J. Mayor-López ◽  
Jacques Weber ◽  
Kaspar Hegetschweiler ◽  
Marc D. Meienberger ◽  
Felix Joho ◽  
...  

RSC Advances ◽  
2014 ◽  
Vol 4 (17) ◽  
pp. 8431-8438 ◽  
Author(s):  
Sadegh Khazalpour ◽  
Davood Nematollahi

Electrochemical behaviour of resazurin in aqueous buffered solutions and ionic liquid was studied. The orientation of adsorbed resazurin was estimated. It is found that, the orientation of the adsorbed resazurin at glassy carbon surface is edgewise.


2022 ◽  
Vol 12 (1) ◽  
Author(s):  
Riyaz Ahmad Dar ◽  
Gowhar Ahmad Naikoo ◽  
Ashwini Kumar Srivastava ◽  
Israr Ul Hassan ◽  
Shashi P. Karna ◽  
...  

AbstractGraphene: zinc oxide nanocomposite (GN:ZnO NC) platform was tried for the sensitive determination of para-nitrophenol (p-NP) through the electrochemical method. ZnO nanoparticles (NPs) were synthesized by the modified wet-chemical method where in potassium hydroxide and zinc nitrate were used as precursors and starch as a stabilizing agent. A green and facile approach was applied to synthesize GN:ZnO NC in which glucose was employed as a reductant to reduce graphene-oxide to graphene in the presence of ZnO NPs. The synthesized NC was characterized using scanning and high-resolution transmission electron microscopy, energy dispersive x-ray analysis, X-ray diffraction and Raman spectroscopic techniques to examine the crystal phase, crystallinity, morphology, chemical composition and phase structure. GN:ZnO NC layer deposited over the glassy carbon electrode (GCE) was initially probed for its electrochemical performance using the standard 1 mM K3[Fe(CN)6] model complex. GN:ZnO NC modified GCE was monitored based on p-NP concentration. An enhanced current response was observed in 0.1 M phosphate buffer of pH 6.8 for the determination of p-NP in a linear working range of 0.09 × 10–6 to 21.80 × 10–6 M with a lower detection limit of 8.8 × 10–9 M employing square wave adsorptive stripping voltammetric technique at a deposition-potential and deposition-time of − 1.0 V and 300 s, respectively. This electrochemical sensor displayed very high specificity for p-NP with no observed interference from some other possible interfering substances such as 2, 4-di-NP, ortho-NP, and meta-NP. The developed strategy was useful for sensitive detection of p-NP quantity in canals/rivers and ground H2O samples with good recoveries.


2020 ◽  
Author(s):  
Miao Liu ◽  
Mingxuan Jia ◽  
Dong Hui Li

Abstract An innovative method for the determination of isoniazid tablets is studied through electrochemical method for the modification of glassy carbon electrode (GCE). Polyoxomolybdate, with stable structures, has not been widely used for the determination of substance. In this study, the mentioned polyoxomolybdate was characterized by Fourier transform infrared spectroscopy (FT-IR), UV-vis, X-ray diffraction (XRD), Atomic force microscope (AFM) and X-ray photoelectron spectroscopy (XPS), and used to modify the glassy carbon electrode. The electrochemical performance of the polyoxomolybdate@GCE was investigated with cyclic voltammetry (CV) and differential pulse voltammetry (DPV), compared with the unmodified electrode, the proposed polyoxomolybdate modified electrode exhibited strong electro-catalytic activities towards isoniazid (INH). Under the optimized conditions, there was linear relationships between the DPV peak currents and the concentrations in the range of 1 × 10 -7 g/L to 3 × 10 -7 g/L for INH (R 2 = 0.9979), with the limit of detection (LOD) of 0.024 μg/L (based on S/N = 3). The modified electrode has proper reproducibility (RSD < 5%), stability, response time (< 3 min) and lifetime (up to 6 days).


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