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Current demands for detection of Gunshot Residue (GSR) require a reliable and rapid decentralized detection system with high sensitivity and specificity. This article reviews the use of electrochemical devices for GSR detection over the last 35 years and highlights recent advances associated with the demands of GSR field detection such as portability, speed, cost and power. Anodic stripping voltammetry (ASV) has been widely implemented for the detection of the metallic components of GSR at a variety of working electrodes. Efforts toward the detection of the organic components of GSR have also been reported using cyclic‐ and square‐wave voltammetry. The simultaneous detection of both organic and inorganic GSR constituents has recently been examined to increase the overall information content in a single voltammetric scan. As well as this, exploitation of screen‐printing fabrication allows replacement of conventional electrochemical cells with easy‐to‐use sensor strips Sampling methods for electrochemical GSR analysis are also advancing from acid washes or swabs to simpler abrasive methods which integrate sampling and analysis obviating the need for intermediate processing steps. The latest direction of electrochemical detection of GSR involves chemometric treatment to evaluate data allowing for more objective conclusions and increasing the automation of the system. These advances indicate great promise for investigating firearm‐related crimes, and bring significant changes to the detection of GSR making electroanalysis a powerful tool for decentralized forensic analysis. 相似文献
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Padmanabhan Santhosh Nagarajan Senthil Kumar Murugesan Renukadevi Anantha Iyengar Gopalan Thiyagarajan Vasudevan Kwang-Pill Lee 《Analytical sciences》2007,23(4):475-478
A glassy carbon electrode modified with a coating of polypyrrole (Ppy) exhibited an attractive performance for the detection and determination of a non-steroidal and non-narcotic analgesic compound, ketorolac tromethamine (KT). Cyclic voltammetry, differential pulse and square wave voltammetry were used in a combined way to identify the electrochemical characteristics and to optimize the conditions for detection. For calibrating and estimating KT, square-wave voltammetry was mainly used. The drug shows a well-defined peak at -1.40 V vs. Ag/AgCl in the acetate buffer (pH 5.5). The existence of Ppy on the surface of the electrode gives higher electrochemical active sites at the electrode for the detection of KT and preconcentrate KT by adsorption. The square-wave stripping voltammetric response depends on the excitation signal and the accumulation time. The calibration curve is linear in the range 1 x 10(-11) to 1 x 10(-7) M with a detection limit of 1.0 x 10(-12) M. Applicability to serum samples was also demonstrated. A detection limit of 1.0 ng ml for serum was observed. Square-wave voltammetry shows superior performance over UV spectroscopy and other techniques. 相似文献
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铂基Pb-Sb表面合金电催化剂的制备与结构表征 总被引:3,自引:1,他引:2
通过电化学方法,在玻碳载体表面制备以Pt、Pb、Sb为主要成分的铂基Pb Sb表面合金电催化剂.运用电化学循环伏安、石英晶体微天平(EQCM)和扫描隧道显微镜(STM)技术对催化剂电极进行表征.结果表明:酸性溶液中在所制备的表面合金电极上,析氢起始电位负移至-0.45 V,表面合金的起始氧化电位为0.15 V,其稳定性明显高于电催化还原中常用的铅、锑等金属电极.通过EQCM研究表面合金电极的形成过程,结合STM观察和XPS深度剖析,确定电催化剂表面是由粒度均匀的纳米颗粒构成的表面合金层. 相似文献
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采用电化学沉积法制备了纳米金修饰玻碳电极,并用循环伏安法和电化学阻抗法进行了表征,以此建立了一种直接测定鸟嘌呤的电分析方法。在磷酸盐缓冲溶液(pH 6.0)中,研究了鸟嘌呤在纳米金修饰电极上的电化学行为,实验结果表明,纳米金修饰电极可以增强鸟嘌呤在电极表面的吸附,并加快鸟嘌呤在电极表面的电子传输,使其电化学信号明显增大,检测灵敏度大大提高,该修饰电极对鸟嘌呤表现出良好的电催化性能。在优化实验条件下对鸟嘌呤进行测定,方法的线性范围为8.0×10-7~6.0×10-5mol/L,检出限为1.0×10-8mol/L,在鸟嘌呤浓度为1.0×10-5mol/L时测得RSD(n=10)为2.5%。 相似文献
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A very sensitive and selective procedure was developed for the determination of niclosamide based on square-wave voltammetry at a glassy carbon electrode. Cyclic voltammetry was used to investigate the electrochemical reduction of niclosamide at a glassy carbon electrode. Niclosamide was first irreversibly reduced from NO2 to NHOH at -0.659 V in aqueous buffer solution of pH 8.5. Reversible and well defined peaks at -0.164 V and -0.195 V (vs. Ag/AgCl) were obtained that are responsible for two electron peaks between NHOH and NO. Following optimisation of the voltammetric parameters, pH and reproducibility, a linear calibration curve over the range 5 x 10(-8)-1 x 10(-6) mol dm(-3) was achieved. The detection limit was found to be 2.05 x 10(-8) mol dm(-3) niclosamide. For eight successive determinations of 5 x 10(-7) mol dm(-3) niclosamide, a relative standard deviation of 2.4% was obtained. This voltammetric method was applied to the direct determination of niclosamide in tablets. The results of the analysis suggest that the proposed method has promise for the routine determination of niclosamide in the products examined. 相似文献
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A Glassy Carbon Electrode Modified with LangmuirBlodgett Film Composed of DNA and Polyaniline for the Sensitive Determination of Salbutamol
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A composite Langmuir? Blodgett film prepared from DNA and polyaniline was deposited on the surface of a glassy carbon electrode (GCE) to give a new voltammetric sensor for the β2‐agonist salbutamol (SAL). Cyclic voltammetry and electrochemical impedance spectroscopy were employed to study the characteristic of the modified electrode. The electrochemistry of SAL at the modified electrode was investigated at pH 6.8 by cyclic voltammetry and differential pulse anodic voltammetry. The oxidation of SAL at this electrode is an adsorption‐controlled irreversible process. A sensitive electroanalytical method for determination of SAL was worked out that displays high precision and good reproducibility. The method was applied to quantify SAL in tablets with satisfactory results. 相似文献
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This study presents a sensitive voltammetric determination of terbutaline (TER) on a platform based on carbon nanotubes (CNTs) and europium oxide nanoparticles (Eu2O3NPs) coated glassy carbon electrodes (GCEs). An ultrasonic bath was performed for the preparation of composite material. The material was characterized by energy dispersive X‐ray spectroscopy (EDX), X‐ray diffraction method (XRD) and scanning electron microscopy (SEM). The Eu2O3NPs/CNTs/GCE system was assessed for the oxidation of terbutaline (TER). A broad oxidation peak was appeared at 0.71 V using a bare GCE. However, the voltammetry of TER has been improved at a GCE coated with CNTs and a well‐defined anodic peak exhibited at 0.61 V. Furthermore, the nanoparticles of Eu2O3 and CNTs coated GCE has greatly improved the electrochemical behaviour of TER and a sharp peak was appeared at 0.59 V. Cyclic voltammetry at Eu2O3NPs/CNTs/GCE also reveals a high catalytic effect for the oxidation of TER with an oxidation peak that is distinctly enhanced compared to GCE and CNTs/GCE. Eu2O3 nanoparticles were utilized to enhance the surface area of GCE and then improve the sensitivity of the procedure. The response of TER was linear over a concentration range of 2.0×10?8 M ?9.5×10?6 M with an LOD of 3.7×10?9 M. Square wave voltammetric analysis of tablets by Eu2O3NPs/CNTs/GCE yielded a recovery of 99.2 % with an RSD% of 3.2. The modified electrode (EuO2NPs/CNTs/GCE) provides accuracy and precision to the analysis of samples. 相似文献
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在抗坏血酸存在下用L-赖氨酸修饰玻碳电极测定多巴胺 总被引:3,自引:0,他引:3
采用电化学氧化法制备了L-广赖氮酸单分子层修饰玻碳电极,研究了多巴胺(DA)和抗坏血酸(AA)在该电极上的电化学行为。结果表明,L-广赖氨酸单分子层修饰玻碳电极不仅能改善多巴胺和抗坏血酸的电化学行为,而且能将多巴胺和抗坏血酸二者在裸电极上的完全重叠的单氧化峰分开成为两个完全独立的氧化峰,循环伏安(CV)图上峰间距为507mV,差分脉冲伏安(DPV)图上峰间距为460mV,由此可实现在AA的共存下对样品中的DA进行选择性测定。 相似文献
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ss—DNA在纳米金上固载和杂化的化学传感研究 总被引:9,自引:0,他引:9
将2-氨乙基硫醇(AET)固载到玻碳电极(GCE)表面,进而化学吸附纳米金(NG),并在纳米金上固载ss-DNA得到ss-DNA/NG/AET/GCE,以Co(bp y)3^3+,但用pH7.0的磷酸缓冲液浸泡可基本上避免这种变性,并时显提高杂化反应的识别能力。结合在ds-DNA/NG/AET/GCE上的Co(bpy)3^3+的峰电流与扫速的线性关系可保持到80mV/s,与电沉积法固载纲米金相比较,本电极更稳定 相似文献
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Timur I. Abdullin Oksana V. Bondar Irina I. Nikitina Emil R. Bulatov Michail V. Morozov Albert Kh. Hilmutdinov Myakzyum Kh. Salakhov Mustafa ulha 《Bioelectrochemistry (Amsterdam, Netherlands)》2009,77(1):37-42
We studied the electrochemical properties of gold nanoparticles (GNPs) and their complexes with proteins using square-wave voltammetry. Effect of the nanoparticle size and detection procedure was explored upon the oxidation of GNPs on a glassy carbon electrode (GCE). For pre-characterized GNPs of 13, 35 and 78 nm diameter, the oxidation peak potential was + 0.98, + 1.03 and + 1.06 V vs. Ag/AgCl, respectively. The conjugation of GNPs with four different proteins was verified by UV–Vis spectroscopy and atomic force microscopy indicated the formation of protein shells around GNPs. This process hampered the oxidation of GNPs on bare GCE causing pronounced decrease in the current response by an average factor of 72. GCE modification with carbon nanotubes weakly influenced the sensitivity of GNP detection but resulted in a 14.5-fold signal increase averaged for all GNP–protein complexes. The acidic dissolution and electrodeposition of GNPs or their complexes adsorbed on GCE allowed superior signal amplification directly proportional to nanoparticle size. The results are useful for the optimization of voltammetric analysis of GNP–protein complexes and can be extended to the characterization of other metal nanostructures and their complexes with biological components. 相似文献
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ss-DNA在纳米金上固载和杂化的电化学传感研究 总被引:1,自引:0,他引:1
将2-氨乙基硫醇(AET)固载到玻碳电极(GCE)表面,进而化学吸附纳米金(NG),并在纳米金上固载ss-DNA得到ss-DNA/NG/AET/GCE,以Co(bpy)33+为电化学指示剂可以识别研究ss-DNA的杂化反应.结果表明,纳米金能使固载其上的ss-DNA发生部分变性而结合Co(bpy)33+,但用pH7.0的磷酸缓冲液浸泡可基本上避免这种变性,并明显提高杂化反应的识别能力.结合在ds-DNA/NG/AET/GCE上的Co(bpy)33+的峰电流与扫速的线性关系可保持到80mV/s.与电沉积法固载纳米金相比较,本电极更稳定和可靠. 相似文献
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《Comptes Rendus Chimie》2015,18(8):823-833
The redox response of three anthracenediones; 4,8-dihydroxy-9,10-dioxo-9,10-dihydroanthracen-1-yl acetate (HACAD), 1,4,5-trihydroxyanthracene-9,10-dione (HAD) and 1,4,5-trihydroxy-2-methyl-3-(3-oxobutyl)anthracene-9,10-dione (HOAD) was probed at the surface of a glassy carbon electrode (GCE) over a wide pH range from pH 3 to pH 12 using voltammetric techniques. Cyclic voltammetry (CV) allowed us to evaluate the redox processes in general. Temperature-dependent sweep rate experiments allowed us to obtain kinetic parameters like the diffusion coefficient and the electron transfer rate constant, which were further used to evaluate the thermodynamics of the processes. Differential pulse voltammetry (DPV) allowed the determination of the number of electrons and protons involved in the Faradaic processes. In addition, square-wave voltammetry (SWV) allowed us to assess the reversible/irreversible nature of the electrode processes and allowed the determination of analytical parameters, such as the limit of detection and the limit of quantification. A thorough UV–vis spectroscopy, in a wide pH range, allowed the determination of the acid-base dissociation constant, pKa, and of the molar extinction coefficient. The pKa values determined by different methods were found to be in very good agreement. 相似文献
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Electrochemical Behavior and Voltammetric Determination of Curcumin at Electrochemically Reduced Graphene Oxide Modified Glassy Carbon Electrode
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This work presents a sensitive voltammetric method for determination of curcumin by using a electrochemically reduced graphene oxide (ERGO) modified glass carbon electrode (GCE) in 100 mM KCl‐10 mM sodium phosphate buffer solution (pH 7.40). The electrochemical behaviors of curcumin at ERGO/GCE were investigated by cyclic voltammetry, suggesting that the ERGO/GCE exhibits excellent electrocatalytic activity towards curcumin, compared with bare GCE and GO/GCE electrodes. The electrochemical reaction mechanisms of curcumin, demethoxycurcumin and bisdemethoxycurcumin at the ERGO/GCE were also investigated and discussed systematically. Under physiological condition, the modified electrode showed linear voltammetric response from 0.2 μM to 60.0 μM for curcumin, with the detection limit of 0.1 μm. This work demonstrates that the graphene‐modified electrode is a promising strategy for electrochemical determination of biological important phenolic compounds. 相似文献
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Burcu Dogan‐Topal Nurgul K. Bakirhan Tugba Taskin Tok Sibel A. Ozkan 《Electroanalysis》2020,32(1):37-49
A sensitive voltammetric technique has been developed for the determination of Fludarabine using amine‐functionalized multi walled carbon nanotubes modified glassy carbon electrode (NH2‐MWCNTs/GCE). Molecular dynamics simulations, an in silico technique, were employed to examine the properties including chemical differences of Fludarabine‐ functionalized MWCNT complexes. The redox behavior of Fludarabine was examined by cyclic, differential pulse and square wave voltammetry in a wide pH range. Cyclic voltammetric investigations emphasized that Fludarabine is irreversibly oxidized at the NH2‐MWCNTs/GCE. The electrochemical behavior of Fludarabine was also studied by cyclic voltammetry to evaluate both the kinetic (ks and Ea) and thermodynamic (ΔH, ΔG and ΔS) parameters on NH2‐MWCNTs/GCE at several temperatures. The mixed diffusion‐adsorption controlled electrochemical oxidation of Fludarabine revealed by studies at different scan rates. The experimental parameters, such as pulse amplitude, frequency, deposition potential optimized for square‐wave voltammetry. Under optimum conditions in phosphate buffer (pH 2.0), a linear calibration curve was obtained in the range of 2×10?7 M–4×10?6 M solution using adsorptive stripping square wave voltammetry. The limit of detection and limit of quantification were calculated 2.9×10?8 M and 9.68×10?8 M, respectively. The developed method was applied to the simple and rapid determination of Fludarabine from pharmaceutical formulations. 相似文献
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通过静电纺丝技术合成碳纳米纤维,以循环伏安法在此碳纤维上电聚合乙酸锌制备复合纳米材料作为一种新型的电化学增敏剂,用于修饰玻碳电极,开发了一种基于碳纤维和氧化锌复合材料的新型电化学传感器(ZnO/CNF/GCE)。使用循环伏安法、差分脉冲伏安法等进行电化学催化性能的研究,并优化实验条件。结果表明,与裸电极相比,在pH 5.5磷酸盐缓冲溶液中,ZnO/CNF/GCE修饰电极能使氧氟沙星的峰电流明显提升,线性范围1~200μmol/L,检测限为0.33μmol/L。该ZnO/CNF/GCE修饰电极已用于氧氟沙星滴耳液中氧氟沙星的含量测定。 相似文献