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Reduction Peak (reduction + peak)
Selected AbstractsElectrochemical Determination of Manganese Solubility in Mercury via Amalgamation and Stripping in the Room Temperature Ionic Liquid n -Hexyltriethylammonium Bis(trifluoromethanesulfonyl)imide, [N6,2,2,2][NTf2]ELECTROANALYSIS, Issue 24 2008Abstract The solubility of manganese in mercury was determined electrochemically via amalgamation and stripping in the room temperature ionic liquid n -hexyltriethylammonium bis(trifluoromethanesulfonyl)imide, [N6,2,2,2][NTf2]. A hemispherical mercury electrode was made by electrodepositing mercury onto a planar platinum microelectrode. Cyclic voltammetry of Mn2+ in [N6,2,2,2][NTf2] at the mercury microhemisphere electrode was investigated at temperatures of 298, 303 and 313,K. The solubility of Mn in Hg was determined on the basis of the charge under the reduction peak (Mn2+,Mn0) and the corresponding reoxidation. [source] Differential Pulse Voltammetric Determination of Selenocystine Using Selenium-gold Film Modified ElectrodeELECTROANALYSIS, Issue 17 2005Yan Bai Abstract Differential pulse voltammetric determination of selenocystine (SeC) using selenium-gold film modified glassy carbon electrode ((Se-Au)/GC) is presented. In 0.10,mol,L,1 KNO3 (pH,3.20) solution, SeC yields a sensitive reduction peak at ,740,mV on (Se-Au)/GC electrode. The peak current has a linear relationship with the concentration of SeC in the range of 5.0×10,8,7.0×10,4,mol,L,1, and a 3, detection limit of SeC is 3.0×10,8,mol,L,1. The relative standard deviation of the reduction current at SeC concentration of 10,6,mol,L,1 is 3.88% (n=8) using the same electrode, and 4.19% when using three modified electrodes prepared at different times. The content of SeC in the selenium-enriched yeast and selenium-enriched tea is determined. The total selenium in ordinary or selenium-enriched tea is determined by DAN fluorescence method. The results indicate that in selenium-enriched yeast about 20% of total selenium is present as SeC and in selenium-enriched tea SeC is the major form of selenoamino acids. The total selenium content in selenium-enriched tea soup is 0.09,,gSe/g accounting by 7% compared with that in selenium-enriched tea. Hence, only a little amount of selenium is utilized by drinking tea, and most selenium still stay in tealeaf. Uncertainty are 22.4% and 16.1% for determination of SeC in selenium-enriched yeast and selenium-enriched tea by differential pulse voltammetry (DPV) on (Se-Au)/GC electrode, respectively. [source] Construction of a novel sensor based on electropolymerization of carmine for voltammetric determination of 4-nitrophenolJOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2007Chunya Li Abstract 4-Nitrophenol (4-NP) has been determined with voltammetric technique based on a novel sensor fabricated by electropolymerization of carmine on a glassy carbon electrode (GCE). An obvious reduction peak located at about ,0.700 V and a couple of redox peaks that were not well-defined were observed in the potential range of ,1.00 to 0.600 V. Compared with its voltammetric behavior on a bare GCE, the reduction peak potential shifted positively and the peak current increased significantly. All experimental parameters were optimized and linear sweep voltammetry was proposed for its determination. In the optimal conditions, the reduction peak current was proportional to the 4-NP concentration over the concentration range from 5.00 × 10,8 to 1.00 × 10,5 mol L,1, and the detection limit was 1.00 × 10,8 mol L,1 after 200 s of accumulation. The high sensitivity and selectivity of the sensor was demonstrated by its practical application for the determination of trace amounts of 4-NP in lake water. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 3271,3277, 2007 [source] ,-Substituted Terthiophene [2]RotaxanesCHEMISTRY - A EUROPEAN JOURNAL, Issue 19 2009Taichi Ikeda Dr. Abstract Towards polythiophene polyrotaxanes: The ,-substituted terthiophene [2]rotaxanes have been synthesized (see figure). Basic optical and electrochemical properties of the synthesized [2]rotaxanes are also reported. Two kinds of ,-substituted terthiophene [2]rotaxanes were synthesized using the host-guest pairs of the electron-deficient cyclophane cyclobis(paraquat- p -phenylene) (CBPQT4+) and the electron-rich terthiophenes with diethyleneglycol chains at the ,-position. One is made from the ,-position non-substituted terthiophene (3,T-,-Rx) and the other is made from the ,-dibromo-substituted terthiophene (3,TBr-,-Rx). The binding constants of the ,-substituted terthiophene threads were confirmed to be smaller than that of the ,-substituted terthiophene analogue. By UV/Vis absorption measurements, we confirmed the charge-transfer (CT) band in the visible region with an extinction coefficient of ,102 (M,1,cm,1). Strong, but not quantitative, quenching of the terthiophene fluorescence was confirmed for the [2]rotaxanes. Although the ,-substituted terthiophene thread was electrochemically polymerizable, the [2]rotaxane 3,T-,-Rx was not polymerizable. This result indicates that the interlocked CBPQT4+ macrocycle effectively suppresses the electrochemical polymerization of the terthiophene unit because electrostatic repulsive and steric effects of CBPQT4+ hinder the dimerization of the terthiophene radical cations. In the electrochemical measurement, we confirmed the shift of the first reduction peak towards less negative potential compared to free CBPQT4+ and the splitting of the second reduction peak. These electrochemical behaviors are similar to those observed for the highly-constrained [2]rotaxanes. The ,-substituted terthiophene [2]rotaxanes reported herein are important key compounds to prepare polythiophene polyrotaxanes. [source] Electrochemical study on interaction of vincristine with tubulinCHINESE JOURNAL OF CHEMISTRY, Issue 11 2001Yong Yu Abstract In Tris (0.005 mol/L)-NaCl (0.05 mol/L) buffer solution (pH = 7.10), keeping temperature at 37°C, a highly sensitive reduction peak of the antitumor agent was obtained by linear sweep voltammetry. The peak potential is-1.56 V (vs. SCE). The peak current is proportional to the concentration of vincristine over the range of 2.1 ± 10,7 -4.2 ± 10,6 mol/L with the detection limit of 1.0 ± 10,7 mol/L. The behavior of the binding of vincristine to tubulin was studied. The results showed that the reaction of tubulin dimer with vincristine formed an electrochemically active complex to be 1:2. Its stability constant is 2.5 ± 1014. The reduction process of the complex is irreversible with adsorptive characteristics. [source] Green Synthesis of Silver Nanoparticles Using Ionic Liquid and Application for the Detection of Dissolved OxygenELECTROANALYSIS, Issue 6 2010Tsung-Hsuan Tsai Abstract The electrochemical synthesis of silver nanoparticles (nano-Ag) has been successfully carried out on glassy carbon electrode (GCE) and indium tin oxide electrode (ITO) using 1-butyl-3-methylimidazolium tetrafluoroborate (BMT) as green electrolytes. Further the electrodeposited nano-Ag modified ITO electrode has been examined using atomic force microscopy (AFM), and X-ray diffraction studies (XRD). The electrodeposited Ag nanoparticles on ITO were found in the size range of 5 to 35,nm. The nano-Ag film modified GCE was further coated with nafion (Nf) and BMT (1,:,1 ratio) mixture and found to be stable in BMT and in pH,7 phosphate buffer solution (PBS). The nano-Ag/BMT-Nf film modified GCE successfully applied for the oxygen reduction reaction in neutral pH (pH,7.0 PBS). The proposed film modified GCE successfully reduces the over potential and show well defined reduction peaks for the detection of dissolved oxygen using cyclic voltammetry (CV) and rotating disc voltammetry (RDE). The film also applied for the detection of dissolved oxygen using electrochemical impedance spectroscopic studies (EIS). [source] The Electrochemical Behavior of Nitrazepam at a Screen-Printed Carbon Electrode and Its Determination in Beverages by Adsorptive Stripping VoltammetryELECTROANALYSIS, Issue 19 2009Natasha Abstract The cyclic voltammetric behavior of nitrazepam was investigated at screen-printed carbon electrodes over the range ,1.5,V to +1.5,V. Two reduction peaks were observable on the negative scan, at ,0.7,V, and ,1.2,V using pH,6 buffer. On the return scan a single oxidation peak was obtained at ,0.05,V. For quantitative analysis of beverages, we developed an anodic adsorptive stripping voltammetric method which required only dilution with buffer. The identification of nitrazepam and flunitrazepam could be achieved using cyclic voltammetry. [source] Characterization and Activity of Cu-MnOx/,-Al2O3 Catalyst for Hydrogenation of Carbon DioxideCHINESE JOURNAL OF CHEMISTRY, Issue 5 2001Gong-Xin Qi Abstract The effect of manganese on the dispersion, reduction behavior and active states of surface of supported copper oxide catalysts have been investigated by XRD, temperature-programmed reduction and XPS. The activity of methanol synthesis from CO2/H2 was also investigated. The catalytic activity over CuO-MnOx/,-Al2O3 catalyst for CO2 hydrogenation is higher than that of CuO/,-Al2O3. The adding of manganese is beneficial in enhancing the dispersion of the supported copper oxide and make the TPR peak of the CuO-MnKx/,-Al2O3 catalyst different from the individual supported copper and manganese oxide catalysts, which indicates that there exists strong interaction between the copper and manganese oxide. For the CuO/,-Al2O3 catalyst there are two reducible copper oxide species; , and , peaks are attributed to the reduction of highly dispersed copper oxide species and bulk CuO species, respectively. For the CuO-MnOx/,-Al2O3 catalyst, four reduction peaks are observed, , peak is attributed to the dispersed copper oxide species; , peak is ascribed to the bulk CuO; , peak is attributed to the reduction of high dispersed CuO interacting with manganese; , peak may be the reduction of the manganese oxide interacting with copper oxide. XPS results show that Cu+ mostly existed on the working surface of the Cu-Mn/,-Al2O3 catalysts. The activity was promoted by Cu with positive charge which was formed by means of long path exchange function between CuOMn. These results indicate that there is synergistic interaction between the copper and manganese oxide, which is responsible for the high activity of CO2 hydrogenation. [source] | ||||||||||