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991.
建立了超声辅助提取/离子色谱法测定铬污染场地中铬(Ⅵ)的方法。选用0.3 mol/L的KCl溶液作提取剂,对12组土壤样品中的铬(Ⅵ)进行超声辅助提取20 min。采用Metrosep A Supp 4-250(250 mm×4.0mm)型阴离子分离柱,以4 mmol/L Na2CO3-1 mmol/L NaHCO3混合溶液为淋洗液对样品进行分离分析。铬(Ⅵ)在0.0120 mg/L浓度范围有较好的线性关系,相关系数(r2)为0.999 8;该方法的检出限为0.003 mg/L,加标回收率为96.4%106.8%,相对标准偏差(RSD,n=3)为0.56%。该方法具有简便、快速、准确等优点,适用于铬污染场地的监测与调查。 相似文献
992.
993.
惰性化学键的活化与重组是近几年来非常热门的研究领域, 同时这个领域也非常富有挑战性. 本文以麻生明教授为首席的国家重点基础研究发展项目(973项目)“惰性化学键的选择性激活、重组及其控制”为基础, 阐述了惰性碳-杂原子键, 碳-氢键, 碳-碳键, 二氧化碳和氧气小分子四个方面的活化和重组, 介绍了一些催化合成的新方法. 这些新方法在完成惰性化学键活化和重组的同时, 也注重于降低污染, 使用更温和的条件, 提高了原子经济性, 为可持续发展战略提供了强有力的技术支持. 相似文献
994.
制备了氧化锆修饰的玻碳电极,采用示差脉冲伏安法和循环伏安法探究了槲皮素在该电极上的电化学行为。结果表明,制备的修饰电极在pH=7.00的磷酸盐缓冲溶液(PBS)中对槲皮素的氧化还原具有明显的电催化作用。采用槲皮素的氧化峰电流作为分析信号。在浓度为2.5×10-8~5×10-5 mol/L的范围内,氧化峰电流和浓度成良好的线性关系,线性方程为ip(μA)=0.0825c-9.861 84,检出限为5.35×10-9 mol/L。 相似文献
995.
Determination of Trichloroacetic Acid (TCAA) Using CdO Nanoparticles Modified Carbon Paste Electrode
In this paper, the electrochemical behavior of a carbon paste electrode modified with CdO nanoparticles as a potential electrocatalyst for the reduction of trichloroacetic acid (TCAA) was investigated using cyclic voltammetry and double‐potential step chronoamperometry. The modified electrode showed a great enhancement in cathodic peak current with respect to reduction of TCAA in acidic aqueous solution. Using this increment, a quantitative method was developed for the determination of TCAA in aqueous solution. The detection limit and linear dynamic range of TCAA are 2.3×10?6 M and 2.3×10?4–3×10?6 M, respectively. 相似文献
996.
Multi‐analyte real‐time interrogation of cellular activity allows for the potential discovery of novel insights into disease. In this report, the addition of electrochemical biosensors to a previously developed platform utilizing Au microfabricated electrodes was explored. Glucose oxidase was immobilized at the electrode surface with an osmium redox polymer, using hand‐casting and electrodeposition techniques, allowing for the first comparison of deposition techniques at a Au microfabricated array. This preliminary work is the first step toward the goal of creating a multi‐analyte array for cellular analysis. 相似文献
997.
Georgina M. S. Alves Júlia M. C. S. Magalhães Helena M. V. M. Soares 《Electroanalysis》2013,25(5):1247-1255
A simple, fast, sensitive and greener voltammetric procedure for simultaneous analysis of nickel (Ni) and cobalt (Co) by square wave adsorptive cathodic stripping voltammetry (SW‐AdCSV) using a solid bismuth vibrating electrode is presented for the first time. The procedure enables to determine Ni together with Co, in ammonia buffer 0.1 M (pH 9.2) and in the presence of oxygen, and involves an adsorptive accumulation of metal‐dimethylglyoxime (Ni‐DMG and Co‐DMG) complexes on the electrode surface. For Ni and Co, the detection limits, obtained with 30 s of accumulation time, were 0.6 and 1.0 µg L?1, respectively. The method was free of metals (Cd2+, Cr3+, Cr6+, Cu2+, Fe3+ and Pb2+ up to 50 µg L?1, Al3+ and Mn2+ up to 500 µg L?1; Zn2+ up to 300 µg L?1) interferences up to the concentrations mentioned in brackets. The proposed method was validated for simultaneous determination of Ni and Co in a certified reference surface and river waters with good results. 相似文献
998.
Self‐assembled monolayers of cucurbit[6]uril (CB[6]) on a gold electrode have been used for 4,4′‐oxydialine (ODA) analysis. The formation of the supramolecular complex between ODA and CB[6] was used for the molecular selection and the electroanalytical determination of this analyte. In addition to this, all the parameters affecting the modification of the gold electrode and the determination of 4,4′‐oxydianiline were optimized by square wave voltammetry. Upon the electrode modification, pentanethiol was employed to fill up the exposed surface between CB[6] molecules. The calculated detection and determination limits were 0.06 µg mL?1 and 0.19 µg mL?1, respectively, with good accuracy and precision as shown by the calculated values for the relative error and relative standard deviation (Er=0.1 % and RDS=2.9 %; n=10 ). Moreover, the developed methodology was successfully applied to the 4,4′‐oxydialine determination in real wastewaters and shoe‐dyeing samples. 相似文献
999.
A highly selective and sensitive electrochemical sensor has been developed by modification of a glassy carbon electrode (GCE) with graphene (GRP) for quantification of Rizatriptan. The significant increase of the peak current and the improvement of the oxidation peak potential indicate that the electrochemical sensor facilitates the electron transfer of Rizatriptan. The oxidation peak current was proportional to the Rizatriptan concentration in the range from 100 to 600 µg/mL with detection (LOD) and quantification limit (LOQ) of 36.52 and 121.73 µg/mL, respectively. The developed method was successfully employed for quantification of Rizatriptan in pharmaceutical formulations. The sensor shows great promise for simple, sensitive and quantitative detection of Rizatriptan. 相似文献
1000.
Wei Sun Yuanyuan Zhang Anhui Hu Yongxi Lu Fan Shi Bingxin Lei Zhenfan Sun 《Electroanalysis》2013,25(6):1417-1424
In this work a partially reduced graphene oxide (p‐RGO) modified carbon ionic liquid electrode (CILE) was prepared as the platform to fabricate an electrochemical DNA sensor, which was used for the sensitive detection of target ssDNA sequence related to transgenic soybean A2704‐12 sequence. The CILE was fabricated by using 1‐butylpyridinium hexafluorophosphate as the binder and then p‐RGO was deposited on the surface of CILE by controlling the electroreduction conditions. NH2 modified ssDNA probe sequences were immobilized on the electrode surface via covalent bonds between the unreduced oxygen groups on the p‐RGO surface and the amine group at the 5′‐end of ssDNA, which was denoted as ssDNA/p‐RGO/CILE and further used to hybridize with the target ssDNA sequence. Methylene blue (MB) was used as electrochemical indicator to monitor the DNA hybridization. The reduction peak current of MB after hybridization was proportional to the concentration of target A2704‐12 ssDNA sequences in the range from 1.0×10?12 to 1.0×10?6 mol/L with a detection limit of 2.9×10?13 mol/L (3σ). The electrochemical DNA biosensor was further used for the detection of PCR products of transgenic soybean with satisfactory results. 相似文献