Home About us Contact
|
Home About us Contact | ||
|
|
||
Conductance Measurements (conductance + measurement)
Selected AbstractsSelection of the eddy currents frequency for conductivity measurements in two-layer structuresPROCEEDINGS IN APPLIED MATHEMATICS & MECHANICS, Issue 1 2009Leszek Dziczkowski Conductance measurements of conductive parts can serve as a background for conclusion about structure of material and possible defects (e.g. fractures, fissures, delamination, flaking, etc.) that may occur in examined parts. When the need arises to test surfaces of parts that are made of a conductive but non-ferromagnetic material, the method of eddy currents offers unsurpassed advantages. The problem refers to application of the eddy current method to examination of conductive material coated with conductive films. The major outcome consists in development of a very simple and useful mathematical model that can be used to determine conductivity of the deep layer for the needs of non-destructive tests. (© 2009 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Internal electrolyte temperatures for polymer and fused-silica capillaries used in capillary electrophoresisELECTROPHORESIS, Issue 22 2005Christopher J. Evenhuis Abstract Polymers are important as materials for manufacturing microfluidic devices for electrodriven separations, in which Joule heating is an unavoidable phenomenon. Heating effects were investigated in polymer capillaries using a CE setup. This study is the first step toward the longer-term objective of the study of heating effects occurring in polymeric microfluidic devices. The thermal conductivity of polymers is much smaller than that of fused silica (FS), resulting in less efficient dissipation of heat in polymeric capillaries. This study used conductance measurements as a temperature probe to determine the mean electrolyte temperatures in CE capillaries of different materials. Values for mean electrolyte temperatures in capillaries made of New Generation FluoroPolymer (NGFP), poly-(methylmethacrylate) (PMMA), and poly(ether ether ketone) (PEEK) capillaries were compared with those obtained for FS capillaries. Extrapolation of plots of conductance versus power per unit length (P/L) to zero power was used to obtain conductance values free of Joule heating effects. The ratio of the measured conductance values at different power levels to the conductance at zero power was used to determine the mean temperature of the electrolyte. For each type of capillary material, it was found that the average increase in the mean temperature of the electrolyte (,TMean) was directly proportional to P/L and inversely proportional to the thermal conductivity (,) of the capillary material. At 7.5,W/m, values for ,TMean for NGFP, PMMA, and PEEK were determined to be 36.6, 33.8, and 30.7°C, respectively. Under identical conditions, ,TMean for FS capillaries was 20.4°C. [source] Thermal and Structural Characterizations of Individual Single-, Double-, and Multi-Walled Carbon NanotubesADVANCED FUNCTIONAL MATERIALS, Issue 24 2009Michael T. Pettes Abstract Thermal conductance measurements of individual single- (S), double- (D), and multi- (M) walled (W) carbon nanotubes (CNTs) grown using thermal chemical vapor deposition between two suspended microthermometers are reported. The crystal structure of the measured CNT samples is characterized in detail using transmission electron microscopy (TEM). The thermal conductance, diameter, and chirality are all determined on the same individual SWCNT. The thermal contact resistance per unit length is obtained as 78,585,m,K,W,1 for three as-grown 10,14,nm diameter MWCNTs on rough Pt electrodes, and decreases by more than 2 times after the deposition of amorphous platinum,carbon composites at the contacts. The obtained intrinsic thermal conductivity of approximately 42,48, 178,336, and 269,343,W,m,1,K,1 at room-temperature for the three MWCNT samples correlates well with TEM-observed defects spaced approximately 13, 20, and 29,nm apart, respectively; whereas the effective thermal conductivity is found to be limited by the thermal contact resistance to be about 600,W,m,1,K,1 at room temperature for the as-grown DWCNT and SWCNT samples without the contact deposition. [source] Variability and Comparison of Hyporheic Water Temperatures and Seepage Fluxes in a Small Atlantic Salmon Stream,GROUND WATER, Issue 1 2003Matthew D. Alexander Ground water discharge is often a significant factor in the quality of fish spawning and rearing habitat and for highly biologically productive streams. In the present study, water temperatures (stream and hyporheic) and seepage fluxes were used to characterize shallow ground water discharge and recharge within the streambed of Catamaran Brook, a small Atlantic salmon (Salmo salar) stream in central New Brunswick, Canada. Three study sites were instrumented using a total of 10 temperature sensors and 18 seepage meters. Highly variable mean seepage fluxes, ranging from 1.7 × 10,4 to 2.5 cm3 m,2 sec,1, and mean hyporheic water temperatures, ranging from 10.5° to 18.0°C, at depths of 20 to 30 cm in the streambed were dependent on streambed location (left versus right stream bank and site location) and time during the summer sampling season. Temperature data were useful for determining if an area of the streambed was under discharge (positive flux), recharge (negative flux), or parallel flow (no flux) conditions and seepage meters were used to directly measure the quantity of water flux. Hyporheic water temperature measurements and specific conductance measurements of the seepage meter sample water, mean values ranging from 68.8 to 157.9 ,S/cm, provided additional data for determining flux sources. Three stream banks were consistently under discharge conditions, while the other three stream banks showed reversal from discharge to recharge conditions over the sampling season. Results indicate that the majority of the water collected in the seepage meters was composed of surface water. The data obtained suggests that even though a positive seepage flux is often interpreted as ground water discharge, this discharging water may be of stream water origin that has recently entered the hyporheic zone. The measurement of seepage flux in conjunction with hyporheic water temperature or other indicators of water origin should be considered when attempting to quantify the magnitude of exchange and the source of hyporheic water. [source] 3,4-Ethylenedioxythiophene,Pyridine-Based Polymers: Redox or n-Type Electronic Conductivity?ADVANCED MATERIALS, Issue 24 2002C.J. DuBois A family of polymers based on alternating bi-EDOT and pyridine units is reported. Poly(BEDOT-PyrPyr-Ph2), with a bandgap of 1.2 eV, has four electrochemically accessible colors (dark gray, burgundy, lime green, and light gray) each corresponding to a distinct redox state. In-situ conductance measurements illustrate high n-type doping conductances only thirty times less than those of the p-type doping conductances. [source] Design of Ceramic Materials for Chemical Sensors: Effect of SmFeO3 Processing on Surface and Electrical PropertiesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2001Hiromichi Aono Perovskite-type SmFeO3 powders were prepared by the thermal decomposition of a heteronuclear complex, Sm(Fe(CN)6)·4H2O and by solid-state reaction between the corresponding single oxides, Sm2O3 and Fe2O3. The thermal decomposition behavior of the complex was studied by thermogravimetric analysis. X-ray diffractometry was used to investigate the structure of the products from the complex thermal decomposition and the formation of SmFeO3 from the oxide mixture. Powders prepared by both methods were used to deposit thick films onto alumina substrates with comb-type gold electrodes. The microstructure and chemical homogeneity of the film surfaces were investigated by scanning electron microscopy and Auger electron spectroscopy. Thick SmFeO3 single-phase films having a homogeneous elemental distribution on the surface were obtained when powder prepared by thermal decomposition of the complex was used for deposition, even when the powder was fired at low temperature (800°C). Surface chemical analysis was performed by X-ray photoelectron spectroscopy (XPS). The O 1s XPS line was deconvoluted into two peaks, attributed to adsorbed oxygen (Oad) and oxygen in the lattice (Olattice). Quantitative analysis showed that the surface coverage of iron, expressed as Fe/(Fe + Sm), was larger for the films prepared using the solid-state reacted powder. Although the Olattice/(Fe + Sm) atomic ratio was not influenced by the processing procedures (and, thus, by iron surface coverage), the amount of Oad decreased with increasing iron surface coverage. A model of the SmFeO3 surface was used to determine that the outermost layer of the perovskite-type SmFeO3 prepared from the complex consisted mainly of samarium ions that could each bond four adsorbed oxygen ions. A single oxygen ion could adsorb onto an iron ion, and therefore, the content of adsorbed oxygen was lower for the film prepared from the solid-state reacted powders, which showed larger iron surface coverage. Electrical conductance measurements, performed with increasing temperature in different gaseous environments, confirmed these findings. Higher conductances and lower activation energies were observed for the films with larger samarium surface coverage. [source] Electronic transport through large quantum dots in the Kondo regimePHYSICA STATUS SOLIDI (B) BASIC SOLID STATE PHYSICS, Issue 2 2003P. Stefa Abstract Conductance through a large two-level quantum dot is investigated theoretically in the strong coupling regime. In large quantum dots the separation between discrete levels becomes smaller than the level width due to strong hybridization with electrodes. In such circumstances, apart from strong electronic correlations in the quantum dot, the indirect interaction between both the spatial levels comes into play. It takes place in lateral quantum dots, where the spatial level index is not conserved during the hybridization process with electrodes. This interaction shifts the Kondo resonance peak in the density of states out of the Fermi surface and alters its intensity. This feature can be observed in the differential conductance dependence vs. bias voltage. The virtual inter-level mixing is suppressed for temperatures above the Kondo temperature of the system. The results of theoretical predictions are compared with the results of experimental conductance measurements performed on large quantum dots and some non-typical conductance features are clarified. [source] Syntheses, characterization and biological studies of zinc(II), copper(II) and cobalt(II) complexes with Schiff base ligand derived from 2-hydroxy-1-naphthaldehyde and selenomethionineAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 10 2010Xueguang Ran Abstract Novel zinc(II), copper(II), and cobalt(II) complexes of the Schiff base derived from 2-hydroxy-1-naphthaldehyde and D, L -selenomethionine were synthesized and characterized by elemental analysis, IR, electronic spectra, conductance measurements, magnetic measurements and powder XRD. The analytical data showed the composition of the metal complex to be ML(H2O), where L is the Schiff base ligand and M = Co(II), Cu(II) and Zn(II). IR results confirmed the tridentate binding of the Schiff base ligand involving azomethine nitrogen, naphthol oxygen and carboxylato oxygen atoms. 1H NMR spectral data of lithium salt of the Schiff base ligand [Li(HL)] and ZnL(H2O) agreed with the proposed structures. The conductivity values of complexes between 12.50 and 15.45 S cm2 mol,1 in DMF suggested the presence of non-electrolyte species. The powder XRD studies indicated that Co(II) complex is amorphous, whereas Cu(II) and Zn(II) complexes are crystalline. The results of antibacterial and antifungal screening studies indicated that Li(HL) and its metal complexes are active, but CuL(H2O) is most active among them. Copyright © 2010 John Wiley & Sons, Ltd. [source] Synthesis, characterization and biological studies of oxovanadium(IV) complexes with triazole-derived Schiff basesAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 2 2010Zahid H. Chohan Abstract A series of triazole-derived Schiff bases (L1,L5) and their oxovanadium(IV) complexes have been synthesized. The chemical structures of Schiff bases were characterized by their analytical (CHN analysis) and spectral (IR, 1H and 13C NMR and mass spectrometry) data, and oxovanadium(IV) complexes were elucidated by their physical (magnetic susceptibility and conductivity), analytical (CHN analysis), conductance measurements and electronic spectral data. The molar conductivity data indicate the oxovanadium(IV) complexes to be non-electrolyte. The Schiff bases act as bidentate and coordinate with the oxovanadium(IV)-forming stoichiometry of a complex as [M (L-H)2] where M = VO and L = L1,L5 in a square-pyramidal geometry. The agar well diffusion method was used for in vitro antibacterial screening against E. coli, S. flexenari, P. aeruginosa, S. typhi, S. aureus and B. subtilis and for antifungal activity against T. longifucus, C. albican, A. flavus, M. canis, F. solani and C. glaberata. The biological activity data show the oxovanadium(IV) complexes to be more antibacterial and antifungal than the parent Schiff bases against one or more bacterial and fungal strains. Copyright © 2009 John Wiley & Sons, Ltd. [source] Ecofriendly synthesis, antimicrobial and antispermatogenic activity of triorganotin(IV) complexes with 4,-nitrobenzanilide semicarbazone and 4,-nitrobezanilide thiosemicarbazoneAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 4 2009Pratibha Chaudhary Abstract New series of triorganotin(IV) complexes with 4,-nitrobenzanilide semicarbazone (L1H) and 4,-nitrobenzanilide thiosemicarbazone (L2H) of the type [R3Sn(L)] (R = -CH3, -C6H5 and n -C4H9) were synthesized under microwave irradiation. All the complexes were characterized by elemental analysis, conductance measurements, molecular weight determinations and spectral data, viz., IR, UV,vis, 1H, 13C and 119Sn NMR. The central tin atoms of these complexes are all five-coordinated with trigonal bipyramidal geometry. In order to assess their growth inhibitory potency semicarbazone, thiosemicarbazone and their triorganotin(IV) complexes were tested in vitro against some pathogenic fungi and bacteria. Also the ligands and their organotin(IV) complexes were studied to assess the effects of long-term ingestion of these compounds on fertility, body and reproductive organ weights. The biochemical analyses were also performed on blood samples and reproductive organs of male rats. The findings have been presented in this paper. Copyright © 2009 John Wiley & Sons, Ltd. [source] Behavioural dynamics in the biological control of pests: role of silicon complexesAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 11 2008Savita Belwal Abstract The complexes of silicon (IV) with Schiff base ligands (L1H and L2H of isatin derivatives) having a sulfur and oxygen donor system were prepared by the reactions in methanol environment. These were isolated and characterized by elemental analysis, molecular weight determinations and conductance measurements. On the basis of electronic, infrared, 1H, 13C and 29Si NMR spectral studies, trigonal bipyramidal geometry was suggested for the resulting complexes. These data support preferential binding of sulfur and oxygen atom to the silicon atom. The disease resistance activities of the ligands and their corresponding complexes were examined successfully in in vitro and in vivo experiments, against pathogenic fungi and bacteria. Results were quite encouraging and these were compared with the standard pesticides Bavistin and Streptomycin. Copyright © 2008 John Wiley & Sons, Ltd. [source] Intramolecular phenylborane complexes with monobasic bidentate Schiff basesAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 2 2007Shweta Gaur Abstract A series of intramolecular complexes with Schiff base ligands having N,S and N,O donor systems were synthesized in an open vessel under microwave irradiation (MWI) using a domestic microwave oven. The reaction time has been brought down from hours to seconds with improved yield as compared with the conventional heating. The complexes have been characterized on the basis of elemental analysis, conductance measurements and spectroscopic analysis. Based on the IR, 1H NMR, 11B NMR and 13C NMR spectroscopic studies, a tetrahedral geometry has been proposed for the resulting complexes. The compounds have been screened in vitro against bacteria and fungi to test their antimicrobial property and in vivo in male albino rats to test their antifertility property. The testicular sperm density, motility and density of cauda epididymal spermatozoa along with biochemical parameters of reproductive organs have been examined and discussed. Copyright © 2007 John Wiley & Sons, Ltd. [source] Spontaneous Organization of Uniform CeO2 Nanoflowers by 3D Oriented Attachment in Hot Surfactant Solutions Monitored with an In Situ Electrical Conductance TechniqueCHEMISTRY - A EUROPEAN JOURNAL, Issue 11 2008Huan-Ping Zhou Abstract Uniform CeO2 nanoflowers were synthesized by rapid thermolysis of (NH4)2Ce(NO3)6 in oleic acid (OA)/oleylamine (OM), by a unique 3D oriented-attachment mechanism. CeO2 nanoflowers with controlled shape (cubic, four-petaled, and starlike) and tunable size (10,40,nm) were obtained by adjusting the reaction conditions including solvent composition, precursor concentration, reaction temperature, and reaction time. The nanoflower growth mechanism was investigated by in situ electrical conductance measurements, transmission electron microscopy, and UV/Vis spectroscopy. The CeO2 nanoflowers are likely formed in two major steps, that is, initial formation of ceria cluster particles capped with various ligands (e.g., OA, OM, and NO3,) via hydrolysis of (NH4)2Ce(NO3)6 at temperatures in the range 140,220,°C, and subsequent spontaneous organization of the primary particles into nanoflowers by 3D oriented attachment, due to a rapid decrease in surface ligand coverage caused by sudden decomposition of the precursor at temperatures above 220,°C in a strong redox reaction. After calcination at 400,°C for 4,h the 33.8,nm CeO2 nanoflowers have a specific surface area as large as 156,m2,g,1 with high porosity, and they are highly active for conversion of CO to CO2 in the low temperature range of 200,400,°C. The present approach has also been extended to the preparation of other transition metal oxide (CoO, NiO, and CuOx) nanoflowers. [source] | ||||||||||||||||