Tìm thấy 20+ kết quả cho từ khóa "Modified electrode"
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The almost semicircle corresponds to the charge transfer process at high frequencies, whereas linear portions correspond to the diffusion process at low frequencies for GCE and modified electrodes. The diameter of the semicircle shows the magnitude of electron-transfer resistance at the electrode surface.
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Recovery analysis of hydrazine determination in Karaçay and Gediz Rivers samples at the modified electrode (n = 3).. doi: 10.1016/j.snb . Gold nanoparticle-modified graphite pencil electrode for the high-sensitivity detection of hydrazine. doi: 10.1016/j.talanta . Nanomolar determination of hydrazine by TiO 2 nanoparticles modified carbon paste electrode. doi: 10.1007/s . Long-term inhalation toxicity of hydrazine.
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Voltammetric determination of itopride using carbon paste electrode modified with Gd doped TiO 2 nanotubes. Carbon paste electrode has been fabricated and mixed with Gd doped and undoped TNT to form a nanocomposite working electrode. Comparison of bare carbon paste electrode and Gd doped and undoped TNT carbon paste electrode for M K 4 [Fe(CN) 6 ] voltammetric analysis. Gd doped TNT modified electrode has been used as working electrode for itopride assay in a pharmaceutical formulation.
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Therefore, this modified electrode is better in clinical applications than the Pt/PPy/GA-Urs electrode.
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The silane agent allows the formation of func- tional groups such as -COOH, -NH 2 , -SH, and -CN, which play roles in the attachment of the biodegradation element to the hydroxylated electrode surface. Nyquist graphs represent the EIS spectra of different layers of the modified electrode.. The diameter of the semicircle is used to calculate the Rct on the electrode surface. The detection range of the designed biosensor was 0.001–10 ng/mL and the detection limit was 10 pg/mL [19].
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Sudan IV Nanotube modified electrode Sudan IV HPLC-DAD . Sudan IV Graphene-modified electrode This work. Under the optimized conditions, the prepared test solution was detected at the graphene-modified GCE by CV. Fortunately, no observable peaks appeared and a recovery experiment was carried out by adding a known amount of Sudan IV to the sample. Recovery of determination of Sudan IV in samples (n = 6).. Content in samples Sudan IV added (M) Average found (M) Recovery.
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The long-term stability of the modified electrode was investigated by examining the peak current response of mol L − 1 VAN, and the modified electrode was stored in 0.1 mol L − 1 at pH 5.2 buffer solution at room temperature during the stability measurements. The current response of the electrode for VAN retained about 97.2% of its initial current after 20 days, which shows that the stability of the modified electrode is good enough for use in long-life voltammetric sensors..
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This relationship was correlated with the characteristics of the diffusion-controlled process at the electrode surface.. Stability of PtNPs/CuPc-CNT film on electrode surface. The stability of the PtNPs/CuPc-CNT film modified electrode was studied by CV measurements. no remarkable change was observed in the current response of the modified electrode stored in the vapor of 0.1 M NaOH solution for 30 days.
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Disposable chitosan*CNT-PGEs have also presented many advantages, being easy to use, sensitive, cost effective, and with good repeatability in comparison to other conventional electrodes, e.g., carbon paste electrode, glassy carbon electrode, and gold electrode.. (A) Nyquist diagrams recorded at bare PGE (a), chitosan modified PGE (b), chitosan and CNT modified PGE (c), and 50 µ g/mL dsDNA immobilized chitosan*CNT PGEs before (d) and after (e) interaction with 40 µ g/mL MC.
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Electrochemical characterization of 1%Pt/Al-SBA-15-GPE electrode material. V for Pt/Al- SBA-15-GPE and V for GPE, respectively. The electrochemical parameters of the 1%Pt/Al-SBA-15-GPE electrode material.. 1%Pt/Al-SBA-15-GPE . SBA-15-GPE. Pt/Al-SBA-15-GPE . Electrochemical impedance spectroscopy measurements at 1%Pt/Al-SBA-15-GPE electrode. Nyquist plots recorded at 1%Pt/Al-SBA-15-GPE modified electrode. EIS fitting parameters for Pt/Al-SBA-15-GPE modified electrodes..
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In the previous studies, the methods suggested for the simultaneous determination of these compounds were carried out using the modified electrode. However, the electrodes used in these methods were expensive, the modification procedure and the polishing and cleaning steps before modification were time-consuming, and not every modified electrode was prepared in the same manner, which affected the reproducibility of the results, making these methods disadvantageous.
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Current–time responses of Ag/PVF-modified Au electrode exposed to UA, AA, DA, and Glu (0.5 mM each) in the presence of 0.5 mM H 2 O 2 at an applied potential of –0.5 V versus SCE.. Reproducibility of Ag/PVF-modified Au electrode studied for 10 days.. A modified electrode system was developed based on Ag nanoparticles supported on conducting PVF film.
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Key words: meso -Tetraphenylporphyrin iron(III) complex, nafion, hydroquinones, chemically modified electrode, redox mediator. 7 Regarding this immobilization of the electrocatalysts into the electrode, an ion-exchange polymer matrix could solve this problem. One of the best solutions to this case might be a platinum electrode coated with Nafion film that contains the immobilized catalyst.
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Figure 3 shows the possible mechanism for the immobilization of PMG at the surface of the modified electrode. Schematic representation of the proposed mechanism for electrodeposition of PMG at the surface of the modified electrode.. exhibited a high stability in the anodic peak current whenever it was placed under ambient conditions in dry state or in phosphate buffer (pH 7.0) for 1 month or longer, showing a good stability of the modified electrode..
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The surface of the glassy carbon electrode was polished on the cloth with 0.1 µm Al 2 0 3 slurry. Scheme shows the mechanism of hydrazine at proposed electrode.. SEM and HRTEM were used for the characterization of the size and morphology of modified electrodes. Electrocatalytic mechanism of the oxidation of hydrazine at AuNPs/(VOx-RuOx)/CNT/GCE..
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Then 10 µL of the prepared composite–acetic acid solution was deposited directly onto the ITO electrode. The electrode was then quickly transferred to a vacuum freeze-dryer, and frozen at –20 ◦ C for 3 h, forming the modified electrode.. Before each test, the modified electrode was immersed into the solution for adsorption under stirring.
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The response of the modified electrode NFMCpE-SDS was examined in 0.5 mmol L − 1 ketotifen/0.1 mol L − 1 PBS of different pH values from 2 to 11 (data not shown). DPV results, the pH value of the solution displayed a great impact on the anodic peak potential and the anodic peak current of ketotifen at the surface of the modified electrode.
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Finally, two polycarbonate wedges are set out parallel to the electrode stack and the pressure is applied on the dry cells thanks to the use of calibrated springs (Fig. The modified electrode preparation consists of the addi- tion of 1–2 wt.% of additives into the original paste formula- tion. The cells are composed of the assembly of three plates in which the modified one is surrounded by the two other polarities and the multi-layer separator is inserted between the plates.
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Zhuangying, P., et al.(2009), Preparation of Hydroxyapatite/Ionic Liquid Composite Film Modified Electrode and Its Application to the Highly Selective Determination of Trace Cadmium in Water
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DPVs obtained at Nf/Pd@CeO2- APTES/GCE working electrode with various concentra- tions of DA. Inset: oxidation peak current of DA versus concentration of DA.. DPVs response of Nf/Pd@CeO 2 -APTES/GCE to and 130 µ M of DA in the presence of and 130 µ M of AA, UA, Glu, and FA.. To investigate the repeatability of Nf/Pd@CeO 2 -APTES/GCE working electrode, five different DPVs were obtained in 0.1 M PBS (pH 7) containing 40 µM DA using the same modified electrode.