Electro measurements

The University developed a method of determination of the material residual strength, based on measurement of the change of phase velocity of ultrasonic waves, as well as an ultrasonic flaw detector-tomograph with multi-element transducers of the type of phased acoustic array. It enables control of the internal structure of materials and products of up to 300 mm thickness, with the resolution of up to 0.5 mm. In the same university, work on NDT is also carried out in the welding and electro-acoustic departments. 

Dir, whereas for small distances d < r), /r Did. The large effective obtainable enables fast heterogeneous reaction rates to be measured under steady-state conditions. Zhou and Bard measured a rate constant of 6 x 10 Ms for the electro-hydrodimerization of acrylonitrile (AN) and observed the short-lived intennediate AN for this process [65]. 

Porschke D and Obst A 1991 An electric field jump apparatus with ns time resolution for electro-optical measurements at physiological salt concentrations Rev. Sc/. Instnim. 62 818-20... 

The 2eta potential (Fig. 8) is essentially the potential that can be measured at the surface of shear that forms if the sohd was to be moved relative to the surrounding ionic medium. Techniques for the measurement of the 2eta potentials of particles of various si2es are collectively known as electrokinetic potential measurement methods and include microelectrophoresis, streaming potential, sedimentation potential, and electro osmosis (19). A numerical value for 2eta potential from microelectrophoresis can be obtained to a first approximation from equation 2, where Tf = viscosity of the liquid, e = dielectric constant of the medium within the electrical double layer, = electrophoretic velocity, and E = electric field. 

Sources of Error. pH electrodes are subject to fewer iaterfereaces and other types of error than most potentiometric ionic-activity sensors, ie, ion-selective electrodes (see Electro analytical techniques). However, pH electrodes must be used with an awareness of their particular response characteristics, as weU as the potential sources of error that may affect other components of the measurement system, especially the reference electrode. Several common causes of measurement problems are electrode iaterferences and/or fouling of the pH sensor, sample matrix effects, reference electrode iastabiHty, and improper caHbration of the measurement system (12). 

Cholesterol The end point for the cholesterol reaction can be determined by following dye formation. Additionally, the amount of oxygen consumed can be measured amperometricaHy by an oxygen-sensing electrode (see Electro analytical techniques). The H2O2 produced by cholesterol oxidase requires phenol to produce dye. 

Mercury layers plated onto the surface of analytical electrodes serve as Hquid metal coatings. These function as analytical sensors (qv) because sodium and other metals can be electroplated into the amalgam, then deplated and measured (see Electro analytical techniques). This is one of the few ways that sodium, potassium, calcium, and other active metals can be electroplated from aqueous solution. In one modification of this technique, a Hquid sample can be purified of trace metals by extended electrolysis in the presence of a mercury coating (35). 

Instmmental methods are useful for the determination of the total silver ia a sample, but such methods do not differentiate the various species of silver that may be present. A silver ion-selective electrode measures the activity of the silver ions present ia a solution. These activity values can be related to the concentration of the free silver ion ia the solution. Commercially available silver ion-selective electrodes measure Ag+ down to 10 flg/L, and special silver ion electrodes can measure free silver ion at 1 ng/L (27) (see Electro analytical techniques). 

Sodium and chloride may be measured using ion-selective electrodes (see Electro analytical techniques). On-line monitors exist for these ions. Sihca and phosphate may be monitored colorimetricaHy. Iron is usually monitored by analysis of filters that have had a measured amount of water flow through them. Chloride, sulfate, phosphate, and other anions may be monitored by ion chromatography using chemical suppression. On-line ion chromatography is used at many nuclear power plants. 

Multienzyme Electrodes. Coupling the reactions of two or more immobilized enzymes increases the number of analytes that can be measured. An electro-inactive component can be converted by an enzyme to a substrate that is subsequentiy converted by a second enzyme to form a detectable end product (57). For example, a maltose [69-79-4] sensor uses the enzymes glucoamylase and glucose oxidase, which convert... 

The three-electrode system serves two important purposes. Because the reference electrode carries no current, but merely measures a potential relative to the working electrode, its stabiUty is not unduly influenced by the electrolysis. Furthermore, because it is placed close to the working electrode the measured potential difference is more nearly representative of the tme potential difference between the working electrode and the sample solution. This latter is the significant quantity in electro analysis. 

Small electrodes allow faster measurements and are therefore very popular with electrochemists. Large solution volumes are typically a few tens of milliliters, but electro analysis can be performed in drops as small as 10 p.L or less because 30 lm times 1 mm equals only 3% of a 10 p.L drop. Preferred analyte concentration ranges are anywhere from subpicomolar to maybe 10 millimolar, depending on the technique employed. 

Velocity transducers are electro-mechanical sensors designed to monitor casing, or relative, vibration. Unlike displacement probes, velocity transducers measure the rate of displacement rather than the distance of movement. Velocity is normally expressed in terms of inches per second (ips) peak, which is perhaps the best method of expressing the energy caused by machine vibration. Figure 43.22 is a schematic diagram of a velocity measurement device. 

Velocity transducers are an electro-mechanical sensor designed to monitor casing or relative vibration. Unlike the displacement probe, velocity transducers measure the rate of displacement not actual movement. Velocity data is... 

Ion-selective bulk membranes are the electro-active component of ion-selective electrodes, which sense the activity of certain ions by developing an ion-selective potential difference according to the Nernst equation at their phase boundary with the solution to be measured. The main differences to biological membranes are their thickness and their symmetrical structure. Nevertheless they are used as models for biomembranes. 

Systematic investigations of the electro-conductivity of niobium-containing fluoride and oxyfluoride melts were not performed. Some measurements were performed on the molten mixtures KCl - K2NbF7, KCl - KF - K2NbF7 by... 

Electro-conductivity measurements were performed on the above systems using the double-electrode method described by Sheiko [325], and are reported in [324],... 

Parker [55] studied the IN properties of MEH-PPV sandwiched between various low-and high work-function materials. He proposed a model for such photodiodes, where the charge carriers are transported in a rigid band model. Electrons and holes can tunnel into or leave the polymer when the applied field tilts the polymer bands so that the tunnel barriers can be overcome. It must be noted that a rigid band model is only appropriate for very low intrinsic carrier concentrations in MEH-PPV. Capacitance-voltage measurements for these devices indicated an upper limit for the dark carrier concentration of 1014 cm"3. Further measurements of the built in fields of MEH-PPV sandwiched between metal electrodes are in agreement with the results found by Parker. Electro absorption measurements [56, 57] showed that various metals did not introduce interface states in the single-particle gap of the polymer that pins the Schottky contact. Of course this does not imply that the metal and the polymer do not interact [58, 59] but these interactions do not pin the Schottky barrier. 

The diffusion current Id depends upon several factors, such as temperature, the viscosity of the medium, the composition of the base electrolyte, the molecular or ionic state of the electro-active species, the dimensions of the capillary, and the pressure on the dropping mercury. The temperature coefficient is about 1.5-2 per cent °C 1 precise measurements of the diffusion current require temperature control to about 0.2 °C, which is generally achieved by immersing the cell in a water thermostat (preferably at 25 °C). A metal ion complex usually yields a different diffusion current from the simple (hydrated) metal ion. The drop time t depends largely upon the pressure on the dropping mercury and to a smaller extent upon the interfacial tension at the mercury-solution interface the latter is dependent upon the potential of the electrode. Fortunately t appears only as the sixth root in the Ilkovib equation, so that variation in this quantity will have a relatively small effect upon the diffusion current. The product m2/3 t1/6 is important because it permits results with different capillaries under otherwise identical conditions to be compared the ratio of the diffusion currents is simply the ratio of the m2/3 r1/6 values. 

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