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1.
The electroanalytical quantification of chloride in [C4mim][BF4], [C4mim][NTf2], and [C4mim][PF6] ionic liquids has been explored using linear sweep and square wave voltammetry. Cathodic stripping voltammetry at a silver disk electrode is found to be the most sensitive. The methodology is based on first holding the potential of the electrode at +2.0 V (vs Ag wire), to accumulate silver chloride at the electrode. On applying a cathodic scan, a stripping wave is observed corresponding to the reduction of the silver chloride. This stripping protocol was found to detect ppb levels of chloride in [C4mim][BF4], [C4mim][NTf2], and [C4mim][PF6]. Although other methods for chloride have been reported for [BF4](-)- and [PF6](-)-based ionic liquids, no methods have been reported for [NTf2](-) ionic liquids.  相似文献   

2.
In this work, the organic compound 2-mercaptobenzimidazole was covalently bound on the surface of a glassy carbon rod, via silanization, yielding a material capable of selectively complexing Hg(2+) ions. This material was applied as an electrode for voltammetric determination of mercury(II) following its nonelectrolytic preconcentration. After exchanging the medium, the voltammetric measurements were carried out by anodic stripping in the differential pulse mode (pulse amplitude, 50 mV; scan rate, 1.25 mV s(-)(1)) using 10(-)(2) mol L(-)(1) NaSCN solution as supporting electrolyte. An anodic stripping peak was obtained at 0.06 V (vs SCE) by scanning the potential from -0.3 to +0.3 V. After a 5 min preconcentration period in a pH 4.0 Hg(2+) solution, this electrode shows increasing voltammetric response in the range 0.1-2.2 μg mL(-)(1), with a relative standard deviation of 5% and a practical detection limit of 0.1 μg mL(-)(1) (5.0 × 10(-)(7) mol dm(-)(3)). Compared with the conventional stripping approach, this chemically modified glassy carbon electrode procedure presented good discrimination against interference from Cu(II) in up to 10-fold molar excess.  相似文献   

3.
A novel method for the detection of arsenic(III) in 1 M HCl at a gold nanoparticle-modified glassy carbon electrode has been developed. The gold nanoparticles were electrodeposited onto the glassy carbon electrode via a potential step from +1.055 to -0.045 V vs SCE for 15 s from 0.5 M H2SO4 containing 0.1 mM HAuCl4. The resulting electrode surfaces were characterized with both AFM and cyclic voltammetry. Anodic stripping voltammetry of arsenic(III) on the modified electrode was performed. After optimization, a LOD of 0.0096 ppb was obtained with LSV.  相似文献   

4.
Electrochemical detection of the rat basophilic leukemia (RBL-1) cells has been carried out by applying cyclic voltammetry. The detection system consists of a basal plane pyrolytic graphite electrode and a porous nitrocellulose membrane filter to trap RBL-1 cells. When the potential of the graphite electrode was run in the range of 0-1.0 V vs SCE, RBL-1 cells gave peak currents at 0.34 V vs SCE as well as 0.65 V vs SCE. There is a linear relationship between the peak current at 0.34 V vs SCE and the cell numbers of RBL-1. In the range of (0.4-2.0) X 10(5) cells. The peak current of RBL-1 cells was attributed to serotonin. When dinitrophenylated bovine serum albumin (DNP-BSA) as a model allergen was added to RBL-1 cells sensitized with anti-DNP IgE, the peak current decreased because of the degranulation of RBL-1 cells leading to serotonin release. On the other hand, RBL-1 cells sensitized with anti-DNP IgE did not respond to egg white, pollens, house dust, and milk.  相似文献   

5.
A novel Nafion/clay-modified electrode (NCME) was developed for the determination of paraquat by square-wave cathodic stripping voltammetry. The clay that showed the best performance for the fabrication of the NCME is nontronite (SWa-1, ferruginous smectite). The electrochemical behavior of paraquat showed that the cathodic peak at -0.70 V vs Ag/AgCl permits adequate quantification of the analyte. Linear calibration curves are obtained over the 0-80 ppb range, with a detection limit of 0.5 ppb in pH 8 phosphate buffer solution for 4 min preconcentration time. Various factors influencing the determination of paraquat were thoroughly investigated in this study. The practical analytical utility is illustrated by selective measurements of paraquat in real water samples.  相似文献   

6.
To more readily evaluate the complex biogeochemistry of selenium, a flow-through electrochemical method was developed that can accurately determine Se(IV) concentrations in aqueous samples to part-per-trillion levels without signal calibration. Stripping methods were used in conjunction with a high-efficiency, flow-through cell. The cell was designed with a novel gold working electrode that was separated from a porous counter electrode by a Nafion membrane. Because this design permitted exhaustive deposition of selenium from the sample stream as well as efficient coulometric stripping, determinations obeyed Faraday's law over a reasonably wide range of operating conditions. The method had a minimum quantitation limit of approximately 8 ng and a maximum limit of 800 ng for Se(IV). It was reliable for sample volumes as small as 0.5 mL and as high as 20 mL, thereby allowing determinations from part-per-million to just below part-per-billion levels. Interferences from Cu(II) and arsenate were evident, but only when these species were present at concentrations exceeding 10 mg.L-1. Overall, the method had a performance comparable to hydride-generation atomic absorption spectrometry but with less cumbersome equipment and freedom from calibration.  相似文献   

7.
N'-acyl-phenylhydrazines (R-Ph-NHNH-COR1) were oxidized in H2O/ CH3CN (1:1) solution pH 11.5 by electrolysis or by the reaction with p- benzoquinone (Q) and the following reactions were investigated using electrochemical methods. The cathodic wave attributed to N'-acyl-N-phenyldiazenes (R-Ph-N = N-COR') was rapidly replaced by a more negative cathodic ivave (half-wave potential = 0.7 V vs. SCE). No other anodic wave was observed, except that of the oxidation of R-Ph-NHNH-COR’. N-Phenyldiazenes (R-Ph-N = NH) might be attacked by Q and R-Ph-N = N-COR' and the cathodic wave observed at - 0.7 V might be attributed to the reduction of the oxidized form of R-Ph-N = NH. The redox potential of R-Ph-N - NH is negative enough to inject electrons directly into the conduction band of silver halides.  相似文献   

8.
Fan C  Wang H  Sun S  Zhu D  Wagner G  Li G 《Analytical chemistry》2001,73(13):2850-2854
Hemoglobin can exhibit a direct electron-transfer reaction after being entrapped in a SP Sephadex membrane. A pair of stable and well-defined redox waves are obtained at a hemoglobin-SP sephadex modified pyrolytic graphite electrode. The anodic and cathodic peak potentials are located at -0.244 and -0.336 V (vs SCE), respectively. On the other hand, the peroxidase activity of the protein in the membrane is also greatly enhanced. The apparent Michaelis-Menten constant is calculated to be 1.9 mM, which shows a large catalytic activity of hemoglobin in the SP Sephadex membrane toward hydrogen peroxide (H2O2). According to the direct electron-transfer property and enhanced peroxidase activity of Hb in the membrane, a Hb/SP Sephadex membrane-based H2O2 biosensor is prepared, with a linear range approximately 5.0 x 10(-6) to 1.6 x 10(-4) mol/L.  相似文献   

9.
This paper describes an electrochemical method for measuring dilute levels of chloride using an underpotentially deposited (UPD) Ag adlayer on polycrystalline Au substrates as a sensing agent. Specifically, chloride ions adsorb onto the Ag UPD adlayer and effect changes in the electrochemical deposition and stripping characteristics of the silver film. Cyclic voltammograms (CVs) of the native Au/Ag(UPD) electrode in 0.1 M H2SO4(aq) exhibit a primary stripping peak for the Ag UPD adlayer at 550 mV vs Ag(+/0), and chloride adsorption onto the Au/Ag(UPD) surface effects a peak shift to approximately 600 mV vs Ag(+/0), depending on the amount of adsorbed Cl-, as affected by the Cl- concentrations and contact times employed in the derivatization. The chloride-treated electrodes also exhibit a stripping peak at 275 mV that is not observed on the native substrate and increases in intensity with Cl- concentration and derivatization time. The integrated charge density for this latter stripping peak relative to that for the primary stripping peak at 550-610 mV provides a useful metric for quantifying adsorbed Cl- levels, and these values allow measurement of Cl- concentrations in dilute aqueous solutions. For Cl- concentrations between 0.5 and 100 microM, the kinetics of Cl- adsorption followed a transient Langmuir adsorption model and allowed measured surface coverages to be used for determining Cl- solution concentrations. Using contact times of 1 min for Cl- adsorption, the electrodes showed a linear response across Cl- concentrations of 0.5-20 microM.  相似文献   

10.
Yang HY  Sun IW 《Analytical chemistry》2000,72(15):3476-3479
A new, and easily fabricated, chemically modified electrode for the determination of selenium(IV) was examined by cathodic square-wave stripping voltammetry. This new electrode consisted of an anion-exchange perfluorinated polymer (Tosflex) coated thin mercury film electrode containing photooxidized 3,3'-diaminobenzidine (ODAB). The coating solution of Tosflex and ODAB was spin-coated on a glassy carbon electrode followed by electroplating of a thin film of mercury. During the preconcentration, ODAB was reduced electrochemically and selenium was accumulated simultaneously onto the electrode by interacting with the reduced ODAB. After a 5-min preconcentration period, linear response was observed from 0.5 to 50 ppb selenium, and the detection limit was 0.1 ppb. The proposed method does not require a darkened room, which was required in many of the previous methods involving 3,3'-diaminobenzidine. In addition, the resistance to interference from surface-active compounds was improved by incorporating Tosflex in the film.  相似文献   

11.
Cui H  Xu Y  Zhang ZF 《Analytical chemistry》2004,76(14):4002-4010
The electrochemiluminescence (ECL) behavior of luminol on a gold nanoparticle self-assembled electrode in neutral and alkaline pH conditions was studied under conventional cyclic voltammetry (CV). The gold nanoparticle self-assembled electrode exhibited excellent electrocatalytic property and redox reactivity to the luminol ECL system. In neutral solution, four ECL peaks were observed at 0.69, 1.03, -0.45, and -1.22 V (vs SCE) on the curve of ECL intensity versus potential. Compared with a bulk gold electrode, two anodic and one cathodic ECL peaks were greatly enhanced, and one new cathodic ECL peak appeared. In alkaline solution, two anodic ECL peaks were obtained at 0.69 and 1.03 V, which were much stronger than those on a bulk gold electrode. These ECL peaks were found to depend on gold nanoparticles on the surface of the electrode, potential scan direction and range, the presence of O(2) or N(2), the pH and concentration of luminol solution, NaBr concentration, and scan rate. The emitter of all ECL peaks was identified as 3-aminophthalate by analyzing the ECL spectra. The spatial distribution of the luminol ECL peaks on the gold nanoparticle self-assembled electrode was studied by CCD. The surface state of the gold nanoparticle self-assembled electrode was characterized by scanning electron microscopy (SEM) and UV-visible reflection spectra. The mechanism for the formation of these ECL peaks has been proposed. The results indicate that the gold nanoparticle self-assembled electrode could lead to novel ECL properties, and strong luminol ECL in neutral and alkaline solutions could be obtained on such an electrode, which is of great analytical potential.  相似文献   

12.
在0.02mol/L硼酸盐缓冲溶液(pH8.7)中,钴(Ⅱ)与酪氨酸生成的络合物在-0.82V(vs.SCE)有一阴极极谱还原峰。基于该极谱行为建立了酪氨酸的分析体系并进行实验条件优化,其浓度在8.0×10-5至4.0×10-4mol/L之间与极谱峰电流呈良好线性关系,检出限为2.8×10-6mol/L。  相似文献   

13.
In this work, the electrogravimetric behavior of copper electrodeposition on TiO2 electrodes was analyzed. Copper electrodeposition was carried out in 0.1 mol L− 1 H2SO4 using several concentrations of CuSO4. The voltammetric curve displays a redox processes. The first redox process occurs in the region of − 0.30 at 0.1 V (vs. saturated calomel electrode, SCE) and it is related to bulk Cu electrodeposition and stripping. For this cathodic process, it was observed that the mass gain increases both as the sweep rate decreases and as the concentration of copper increases. The second redox process, which occurs between − 0.1 V and 0.35 V (vs. SCE), the stripping charge (and mass) are independent of both sweep rate and CuSO4 concentration and, finally, there is a saturation charge (and saturation mass) as the deposition time is increased. From the saturated mass, obtained using an electrochemical quartz crystal nanobalance, for this electrodeposition process (248 ng cm− 2) a roughness factor of 1.8 was calculated for the TiO2 film.  相似文献   

14.
An electrochemical immunoassay for cardiac troponin I (cTnI) combining the concepts of the dual monoclonal antibody "sandwich" principle, the silver enhancement on the nano-gold particle, and the anodic stripping voltammetry is described. Four main steps were carried out to obtain the analytical signal, i.e., electrode preparation, immunoreaction, silver enhancement, and anodic stripping voltammetric detection. A linear relationship between the anodic stripping peak current and concentration of cTnl from 1 to 20 ng/ml and a limit of detection of 0.8 ng/ml were obtained. The established method was tested by determining cTnI in acute myocardial infarction (AMI) samples using enzyme-linked immunoadsorbent assay (ELISA) for comparison analysis, and good results were obtained.  相似文献   

15.
The electrochemical activity of Au electrodes held at constant potential for anodic detection of carbohydrates in alkaline media eventually decays to zero. This loss of response is a consequence of the accumulation of adsorbed oxidation products on the electrode surface. Although it is well-known that these "poisons" can be removed by oxidative desorption simultaneously with formation of surface oxide, we have discovered that electrodes fouled during the detection of glucose yield a cathodic peak at -0.77 V vs SCE resulting from reductive desorption of these species. Incorporation of the reductive desorption process into wave forms for pulsed electrochemical detection (PED) permits a significant decrease in the time periods traditionally allowed for the oxidative and reductive reactivation of the electrode with a resulting increase in wave form frequency. A 6.7-Hz wave form using E(red) = -1.00 V (t(red) = 10 ms), E(oxd) = +0.60 V (t(oxd) = 10 ms), and E(det) = +0.10 V (t(del) = 50 ms, t(int) = 50 ms) is applied for detection of glucose in a LC-PED system and is demonstrated to yield a sub-picomole detection limit with a linear dynamic range extending over three decades.  相似文献   

16.
示波极谱法快速测定水样中微量镍   总被引:1,自引:0,他引:1  
孙莉 《福建分析测试》2010,19(1):83-84,87
在pH9.6的Na2B4O7电解质中,镍和丁二酮肟在-1060mV(vs.SCE)处产生灵敏的络合吸附波,峰电流与镍的浓度在1.0×10-3~25μg/mL范围内呈线性关系,检出限为0.12ng/mL。该方法仪器试剂简单,操作快速简便,用于测定水样中微量镍,结果满意。  相似文献   

17.
The paradoxical appearance of a cathodic reaction sometimes observed in anodic stripping voltammetry and stripping potentiometry when using mercury film electrodes in chloride media containing mercury(II) has been investigated by systematically varying relevant chemical and electrochemical parameters and comparing the results with thermodynamic equilibrium calculations. Microscopic observations of morphological changes on the electrode surface caused by potential variations were made possible by using a novel electrode design. Three conditions have to be fulfilled for the cathodic reaction to occur: (a) formation of calomel by reaction between elemental mercury on the electrode surface and mercury(II) in solution, (b) subsequent reduction of mercury(II) to elemental mercury on the calomelized electrode surface, and (c) a chloride concentration in the range 0.001-3.5 M. Different ways of avoiding the interference from the cathodic reaction in stripping voltammetry and stripping potentiometry are experimentally demonstrated, and a mechanism for the appearance of the cathodic reaction is proposed.  相似文献   

18.
Xu S  Liu Y  Wang T  Li J 《Analytical chemistry》2011,83(10):3817-3823
In this work, we report a cathodic electrogenerated chemiluminescence (ECL) of luminol at a positive potential (ca. 0.05 V vs Ag/AgCl) with a strong light emission on the graphene-modified glass carbon electrode. The resulted graphene-modified electrode offers an excellent platform for high-performance biosensing applications. On the basis of the cathodic ECL signal of luminol on the graphene-modified electrode, an ECL sandwich immunosensor for sensitive detection of cancer biomarkers at low potential was developed with a multiple signal amplification strategy from functionalized graphene and gold nanorods multilabeled with glucose oxidase (GOx) and secondary antibody (Ab(2)). The functionalized graphene improved the electron transfer on the electrode interface and was employed to attach the primary antibody (Ab(1)) due to it large surface area. The gold nanorods were not only used as carriers of secondary antibody (Ab(2)) and GOx but also catalyzed the ECL reaction of luminol, which further amplified the ECL signal of luminol in the presence of glucose and oxygen. The as-proposed low-potential ECL immunosensor exhibited high sensitivity and specificity on the detection of prostate protein antigen (PSA), a biomarker of prostate cancer that was used as a model. A linear relationship between ECL signals and the concentrations of PSA was obtained in the range from 10 pg mL(-1) to 8 ng mL(-1). The detection limit of PSA was 8 pg mL(-1) (signal-to-noise ratio of 3). Moreover, the as-proposed low-potential ECL immunosensor exhibited excellent stability and reproducibility. The graphene-based ECL immunosensor accurately detected PSA concentration in 10 human serum samples from patients demonstrated by excellent correlations with standard chemiluminescence immunoassay. The results suggest that the as-proposed graphene ECL immunosensor will be promising in the point-of-care diagnostics application of clinical screening of cancer biomarkers.  相似文献   

19.
Lin D  Wu J  Wang M  Yan F  Ju H 《Analytical chemistry》2012,84(8):3662-3668
A triple signal amplification strategy was designed for ultrasensitive immunosensing of cancer biomarker. This strategy was achieved using graphene to modify immunosensor surface for accelerating electron transfer, poly(styrene-co-acrylic acid) microbead (PSA) carried gold nanoparticles (AuNPs) as tracing tag to label signal antibody (Ab(2)) and AuNPs induced silver deposition for anodic stripping analysis. The immunosensor was constructed by covalently immobilizing capture antibody on chitosan/electrochemically reduced graphene oxide film modified glass carbon electrode. The in situ synthesis of AuNPs led to the loading of numerous AuNPs on PSA surface and convenient labeling of the tag to Ab(2). With a sandwich-type immunoreaction, the AuNPs/PSA labeled Ab(2) was captured on the surface of an immunosensor to further induce a silver deposition process. The electrochemical stripping signal of the deposited silver nanoparticles in KCl was used to monitor the immunoreaction. The triple signal amplification greatly enhanced the sensitivity for biomarker detection. The proposed method could detect carcinoembryonic antigen with a linear range of 0.5 pg mL(-1) to 0.5 ng mL(-1) and a detection limit down to 0.12 pg mL(-1). The immunosensor exhibited good stability and acceptable reproducibility and accuracy, indicating potential applications in clinical diagnostics.  相似文献   

20.
Superconducting thin films of Bi(Pb)-Sr-Ca-CuO system were prepared by depositing the film onto silver substrate by d.c. electrodeposition technique with dimethyl sulphoxide bath in order to examine the effect of Pb addition to the BSCCO system. The films were deposited at the potential of -0.8 V vs saturated calomel electrode (SCE) onto the silver substrate. The different preparative parameters such as deposition potential, deposition time were studied and optimized. These films were then oxidized electro-chemically at room temperature in an alkaline (1 N KOH) solution, and also at 600°C temperature in an oxygen atmosphere. The films showed the superconducting behaviour, with Tc values ranging between 85 K and 96 K, respectively.  相似文献   

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