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Xem 1-20 trên 110 kết quả Voltammetry
  • Bài viết trình bày đặc trưng phổ và điện hóa của TCNQF4(2,3,5,6-Tetraflo-7,7,8,8-Tetracyanoquinondimetan) và các anion của TCNQF4n. Các kết quả này có thể được sử dụng để nghiên cứu và phân tích cho các sản phẩm khác được tạo thành từ TCNQF4.

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  • In the paper "Experimental and theoretical studies on the composite composed of graphene oxide and polyaniline", we report theoretical and experimental results on graphene oxide – polyaniline composites. Experimental results in this study were obtained by using different techniques: X-ray diffraction (XRD), Scanning electron microscope (SEM) and from cyclic voltammetry. The theoretical results were acquired using method of density functional theory (DFT).

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  • A simple approach to constructing a double-layer voltammetric sensor is described. The poly(malachite green) (PMG) and multiwalled carbon nanotubes (MWCNTs) were coimmobilized at the surface of the glassy carbon electrode (GCE) for fabrication of PMG/MWCNT/GCE. The modified electrode was characterized by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), differential pulse voltammetry (DPV), and chronoamperometric techniques.

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  • In this study, electrochemical behaviors of formazans were investigated. The compounds contained CH3 and OCH3 groups at the o-, m-, and p-positions of the 1-phenyl ring and an OCH3 group at the p-position of the 3-phenyl ring. Their electrochemical behaviors, such as the number of electrons transferred, diffusion coefficients, and heterogeneous rate constants, were studied by cyclic voltammetry, ultramicrodisk electrode, and chronoamperometry. Possible mechanisms were proposed based upon the data obtained.

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  • Adsorptive cathodic stripping voltammetric determination of aluminum at ng mL −1 levels in salt samples based on the metal complexation with Calcon (1-(2-hydroxynaphthylazo)-2 naphthol-4-sulfonic acid) and the subsequent adsorptive deposition onto a hanging mercury drop electrode was studied. Central composite design was used as a design method. Several chemical and instrumental parameters (pH, ligand concentration, deposition time, deposition potential, and complexing time) were involved in the experimental design.

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  • The electrochemical oxidation of 2,6-diaminopurine (2,6-DAP) was studied in pH 7.4 phosphate buffer solution on multiwall carbon nanotube modified glassy carbon electrode (MWCNT/GCE) over a temperature range of 20 to 50 ◦ C using cyclic voltammetry. 2,6-DAP oxidation on MWCNT/GCE showed a well-defined and irreversible oxidation peak at about 0.72 V vs. Ag/AgCl at pH 7.4. The oxidation potential of 2,6-DAP linearly varied with pH over the range of 3.0 to 10.0 with a slope of –0.0547 V/pH, implying that 2 protons were accompanied by 2 electrons transferred in the electrochemical reaction.

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  • This paper describes a sensitive and accurate adsorptive catalytic stripping voltammetric method for the determination of zineb (zinc ethylene-bis- dithiocarbamate) in tap water and tomato samples. The method is based on the reduction of adsorbed zineb at a hanging mercury drop electrode following its catalytic oxidation using peroxydisulfate as an oxidizing reagent. Chemical and instrumental parameters of the process were optimized.

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  • A simple and sensitive modified electrode was fabricated with graphene via the drop-casting method and applied for the electrochemical detection of Sudan IV. Cyclic voltammetry (CV) was used to investigate the electrochemical behaviors of Sudan IV in phosphate buffer solution (PBS). The experimental conditions such as determining medium, scan rate, and accumulation time were optimized for the determination of Sudan IV.

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  • The effects of propargyl alcohol (PA), propynol ethoxylate (PME), propargyl sulfonate (PS), and diethylaminopropyne (DEP) compounds as additives in a Watts bath on coating brightness, thickness, and efficiency were investigated and compared using electrochemical methods such as linear and square wave voltammetry (SWV), chronoamperometry, chronopotentiometry, electrochemical impedance (EIS), and X-ray fluorescence (XRF) spectroscopy.

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  • The synthesis of novel, symmetrical, tetrasubstituted manganese phthalocyanine complexes bearing 4 hexylthio, 2’,3’,4’,5’,6’-pentafluorobenzyloxy, 2’,3’,5’,6’-tetrafluoro-4’-hexylthio-benzyloxy, and 2’,3’,5’,6’-tetrafluoro-4’- pentoxy-benzyloxy units is reported. The new compounds have been characterized by using elemental analyses and UV-Vis, FT-IR, and mass spectroscopic data. The electrochemical properties of the manganese phthalocyanine complexes were investigated by cyclic and square wave voltammetry and the nature of the observed redox processes was studied by spectroelectrochemistry.

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  • Single-walled carbon nanotube (CNT) and chitosan composite (chitosan*CNT) based sensors were developed as DNA biosensors, and then they were applied for electrochemical investigation of the interaction between the anticancer drug mitomycin C (MC) and DNA. The oxidation signals of MC and guanine were monitored before and after the interaction process by differential pulse voltammetry (DPV). The DPV results were in good agreement with those of electrochemical impedance spectroscopy (EIS).

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  • The reduction behavior of fenoxaprop-p-ethyl (FNX) was studied on a hanging mercury drop electrode. FNX showed 2 reduction peaks at about –0.7 V and at about –0.9 V versus Ag/AgCl/3.0 M KCl in Britton–Robinson buffer at pH 4.8. Both reductions were irreversible and adsorption was effective. The reduction peaks were assigned to the reduction of C=N to CH–NH and the reduction of C=O to CH–OH. Square-wave voltammetry has been proposed and validated for quantification of FNX in different samples.

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  • Methyl 4-((9H-(carbazole-9-carbanothioylthio) benzoate (MCzCTB) was chemically synthesized and characterized by FTIR, 1H NMR, and 13C NMR. A novel synthesized monomer was electropolymerized on a glassy carbon electrode (GCE) in various initial molar concentrations of [MCzCTB] 0 = 1,3,5, and 10mM in 0.1M NaClO4/CH3CN and 1M H2SO4. P(MCzCTB)/GCE was characterized by cyclic voltammetry, Fourier transform infrared-attenuated transmittance reflectance, scanning electron microscopy-energy dispersive X-ray, and electrochemical impedance spectroscopy.

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  • In this study peripherally tetra-substituted metal-free, metallophthalocyanines bearing (3,4-dimethoxybenzyl) oxy groups have been synthesized and characterized. Electrochemical properties of novel phthalocyanines 4, 5, 6, and 7 were determined by cyclic and square wave voltammetry in order to define their possible applications in different electrochemical technologies. CoII and TiIVO metal ions behave as redox active cations in the core of the CoPc and TiOPc complexes, respectively

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  • The electrochemical behavior of valproic acid (VAL) was investigated using square wave voltammetry, cyclic voltammetry, and sampled direct current polarography and a new square wave voltammetric method was developed for determination of VAL in pharmaceutical preparations. Recovery studies for the accuracy of the method were performed by adding known amounts of VAL and it was found to be 109.67 ± 4.85%. The proposed method was successfully applied to pharmaceutical products on the market.

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  • The prepared materials were characterized by using BET, TGA, XRD, and TEM techniques. Cyclic voltammetry was used in order to determine the electrocatalytic activity of the prepared catalyst for hydrogen oxidation and oxygen reduction reactions that occur in proton exchange membrane fuel cells (PEMFCs). The Pt loading obtained over the composite material was around 10%. TEM results showed highly dispersed and small nanoparticles over the composite material by using scCO2 deposition.

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  • The present paper describes the use of a disposable pencil graphite electrode (PGE) for the voltammetric determination of famotidine. Cyclic voltammetric studies using different supporting electrolytes emphasized an irreversible oxidation of famotidine on the PGE. The electrode process is diffusion-controlled and pH-dependent. Differential pulse voltammetry (DPV) in phosphate buffer solution of pH 6.81 was employed for famotidine’s quantitative determination.

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  • This paper presents the results of an investigation of the properties of a modified platinum electrode with meso-tetraphenylporphyrin iron(III) complex immobilized in Nafion film and its catalytic activity in the electrochemical oxidation of selected hydroquinone and catechol derivatives. The redox activity of iron complexes of porphyrins was characterized in aqueous solutions of perchloric acid by means of cyclic voltammetry and differential pulse voltammetry.

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  • The electrochemical reduction of 2-[8-hydroxyquinoline-5-yl)azo]benzo[c]cinnoline was investigated by cyclic voltammetry, controlled potential electrolysis, and chronoamperometry techniques in the presence of 0.10 mol L−1 tetrabutylammonium tetrafluoroborate in dimethyl sulfoxide at platinum electrode. 2-[8-Hydroxyquinoline-5-yl)azo]benzo[c] cinnoline displays three sharp cathodic peaks and three anodic peaks in the cyclic voltammogram. The diffusion coefficients and the number of electrons transferred were calculated by using an ultramicroelectrode and platinum electrode.

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  • Four different Mannich base derivatives containing an aromatic/heteroaromatic propanone structure (C1 (3-(dimethylamino)-1-(thiophen-2-yl)propan-1-one hydrochloride); C2 (3-morpholino-1-(pyridin-3-yl)propan-1-one hydrochloride); C3 (3-(dimethylamino)-1-(1H -indol-3-yl)propan-1-one hydrochloride), C4 (3-(piperidin-1-yl)-1-(pyren-1- yl)propan-1-one hydrochloride)) were earlier synthesized and characterized with 1 H NMR, 13 C NMR, MS, and elemental analysis.

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