Copper Electrodes (copper + electrode)

Distribution by Scientific Domains


Selected Abstracts


Fabrication of Nanoporous Copper Film for Electrochemical Detection of Glucose

ELECTROANALYSIS, Issue 21 2009
Sirilak Sattayasamitsathit
Abstract A nanoporous copper film was fabricated on a copper wire by electrodeposition of copper/zinc alloy and chemically etching of zinc. The surface morphology was investigated by SEM. When applied to detect glucose in an amperometric flow injection system the porous copper electrode provided 12 times higher sensitivity than solid copper. It could be continuously used up to 50 times (%RSD=5.7). Different preparations of the porous film provided reproducible responses (P<0.05). Detection of glucose in E. coli cultivation medium compared well with spectrophotometric technique (P<0.05). This simple technique can produce a nanoporous electrode with good performances and can easily be applied to other metals and analytes. [source]


CE with electrochemical detection for investigation of label-free recognition of amino acid amides by guanine-rich DNA aptamers

ELECTROPHORESIS, Issue 17 2007
Tao Li
Abstract In this work, we report a simple and effective investigation into adaptive interactions between guanine-rich DNA aptamers and amino acid amides by CE with electrochemical (EC) detection. Argininamide (Arm) and tyrosinamide (Tym) were chosen as model molecules. On a copper electrode, Arm generated a good EC signal in 60 mM NaOH at 0.7 V (vs Ag/AgCl), while Tym was detected well on a platinum electrode at 1.3 V in 20 mM phosphate of pH 7.0. Based on their EC properties, the ligands themselves were used as indicators for the adaptive interactions investigated by CE-EC, making any step of labeling and/or modification of aptamers with indicators exempted. Hydrophilic ionic liquid was used as an additive in running buffer of CE to improve the sensitivity of Arm detection, whereas the additive was not used for Tym detection due to its negative effect. Two guanine-rich DNA aptamers were used for molecular recognition of Arm and Tym. When the aptamers were incubated with ligands, they bound the model molecules with high affinity and specificity, reflected by obvious decreases in the signals of ligands but no changes in those of the control molecules. However, the ligands were hardly affected by the control ssDNAs after incubation. The results revealed the specific recognition of Arm and Tym by the aptamers. The mechanisms for binding model molecules by aptamers were discussed. Not as expected, these aptamers were not to form the G-quartets, which were generally responsible for binding the ligands when the guanine-rich aptamers were used. [source]


Disposable Amperometric Sensors for Thiols with Special Reference to Glutathione

ELECTROANALYSIS, Issue 18 2008
Dipankar Bhattacharyay
Abstract The antioxidant ,reduced glutathione' tripeptide is conventionally called glutathione (GSH). The oxidized form is a sulfur-sulfur linked compound, known as glutathione disulfide (GSSG). Glutathione is an essential cofactor for antioxidant enzymes; it provides protection also for the mitochondria against endogenous oxygen radicals. The ratio of these two forms can act as a marker for oxidative stress. The majority of the methods available for estimation of both the forms of glutathione are based on colorimetric and electrochemical assays. In this study, electrochemical sensors were developed for the estimation of both GSH and GSSG. Two different types of transducers were used: i) screen-printed three-electrode disposable sensor (SPE) containing carbon working electrode, carbon counter electrode and silver/silver chloride reference electrode; ii) three-electrode disposable system (CDE) consisting of three copper electrodes. 5,5,-dithiobis(2-nitrobenzoic acid) (DTNB) was used as detector element for estimation of total reduced thiol content. The enzyme glutathione reductase along with a co-enzyme reduced nicotinamide adenine dinucleotide phosphate was used to estimate GSSG. By combining the two methods GSH can also be estimated. The detector elements were immobilized on the working electrodes of the sensors by bulk polymerization of acrylamide. The responses were observed amperometrically. The detection limit for thiol (GSH) was less than 0.6,ppm when DTNB was used, whereas for GSSG it was less than 0.1,ppm. [source]


Multilayer Construction with Various Ceramic Films for Electronic Devices Fabricated by Aerosol Deposition

INTERNATIONAL JOURNAL OF APPLIED CERAMIC TECHNOLOGY, Issue 6 2006
Hironori Hatono
Aerosol deposition (AD) is applicable as a fabrication technology for microstructures comprising different materials. We used this method for electronic devices that consist of ceramic films and metal electrodes. Various ceramic thick films (5,50 ,m thickness), for example, Al2O3, 2MgO·SiO2, and BaTiO3, were deposited on substrates using room-temperature aerosol deposition. The dielectric constant of BaTiO3 was 78 at 1 MHz. Multilayer constructions with ceramic films and copper electrodes were obtained using aerosol deposition and sputtering. During deposition, photoresist film masks were applied to produce patterns of ceramic films and connections between upper and lower electrodes through the ceramic films. [source]


Kinetics of Electrophoretic Deposition for Nanocrystalline Zinc Oxide Coatings

JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2004
Yuan-Chung Wang
An integrated process combining the preparation of ZnO nanoparticles and the formation of ZnO coatings using electrophoretic deposition (EPD) is reported. The work focuses on the deposition kinetics of nanocrystalline ZnO coatings on copper electrodes during EPD by direct measurement of the thickness of the deposited layer. The experimental results show that the EPD process is a powerful route to fabricate uniform coatings with desired thickness and excellent surface smoothness, which might be attributed to small particle size and narrow size distribution. On the other hand, the deposition kinetics changes with applied voltage and deposition time. The deposition thickness increases with increasing applied voltage and deposition time. In a short deposition time, the deviation of deposition rate between the theoretical and experimental values is caused by voltage drops during deposition, and the discrepancy increases with the applied voltage. Moreover, the increasing voltage drop and depletion of the suspension lead to decreasing current and lower deposition rate after longer deposition time. The critical transition time of deposition kinetics is found to exponentially decrease with increasing applied voltage. [source]


Non-mass-dependent oxygen isotopic fractionation in smokes produced in an electrical discharge

METEORITICS & PLANETARY SCIENCE, Issue 7-8 2007
Yuki Kimura
The smokes were formed at the Goddard Space Flight Center (GSFC) at total pressures of just under 100 Torr in an electrical discharge powered by a Tesla coil, were collected from the surfaces of the copper electrodes after each experiment and sent to the University of California at San Diego (UCSD) for oxygen isotopic analysis. Transmission electron microscopy studies of the smokes show that they grew in the gas phase rather than on the surfaces of the electrodes. We hypothesize at least two types of fractionation processes occurred during formation of the solids: a mass-dependent process that made isotopically lighter oxides compared to our initial oxygen gas composition followed by a mass-independent process that produced oxides enriched in 17O and 18O. The maximum ,17O observed is + 4.7, for an iron oxide produced in flowing hydrogen, using O2 as the oxidant. More typical displacements are 1,2, above the equilibrium fractionation line. The chemical reaction mechanisms that yield these smokes are still under investigation. [source]