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Transport microscopic measurement

The methods of measuring the velocity of electrokinetic motion are fully described in some of the reviews mentioned above. They include (for cataphoresis) various forms of U-tube in which the motion of the boundary of the suspension is observed, transference methods similar to Hittorf s transport number measurements in electrochemistry, and microscopic cells in which the motion of individual particles is watched, due allowance being made for the motion of the suspending fluid in the opposite direction to the particles. Sumner and Henry s device1 of fixing a sphere on a fibre and observing its deflexion in a horizontal electric field is very ingenious, and not so frequently mentioned as other methods. [Pg.352]

Microscopic Measurement of Transport Diffusion and Permeation Through Transport Resistances on the Crystal Surface... [Pg.181]

Originally SECM has been worked out for voltammetric detection. Ever since, in most of the electrochemical microscopic measurements amperometric data collection is employed. In amperometry an appropriate constant electrode potential is imposed on a working electrode and the current is followed in time. The current shows the rate of the overall electrode reaction. The transport of the electroactive species toward the electrode surface is the rate determining step of this reaction. [Pg.285]

A most recent commercial Nano Indenter (Nano Indenter XP (MTS, 2001)) consists of three major components [66] the indenter head, an optical/atomic force microscope, and x-y-z motorized precision table for positioning and transporting the sample between the optical microscopy and indenter (Fig. 28). The load on the indenter is generated using a voice coil in permanent magnet assembly, attached to the top of the indenter column. The displacement of the indenter is measured using a three plate capacitive displacement sensor. At the bottom of the indenter rod, a three-sided... [Pg.22]

Alternatively, a higher rate of mass transport in steady-state measurements with a larger UME can be obtained by using it as a tip in the scanning electrochemical microscope (SECM). The SECM has typically been employed for probing interfacial ET reactions [29]. Recently, micropipettes have been used as SECM probes (see Section IV.B below) [8b,30]. Although the possibility of probing simple and assisted IT at ITIES by this technique was demonstrated, no actual kinetic measurements have yet been reported. [Pg.392]

While the previously described techniques were measuring the nanoscopic and microscopic properties of the catalyst pellets, respectively, fluid transport within... [Pg.272]

Because of the possible effects of active and carrier-mediated processes and metabolic biotransformation, the issue of tissue viability is important for in vitro buccal mucosal experiments. The barrier nature of the buccal mucosa resides in the upper layers of the epithelium, where unlike in the stratum corneum, the cells contain a variety of functional organelles [119, 122, 125, 150], and so tissue viability may be an important component of the barrier function of the tissue. Various methods have been employed to assess the viability of excised buccal mucosa, including measurement of biochemical markers, microscopic methods, and linearity of transport data [42], While biochemical methods, including measurement of adenosine 5 -triphosphate (ATP) levels and utilization of glucose, provide information on the metabolic activity of the tissue, this does not necessarily relate to the barrier function of the tissue. In excised rabbit buccal mucosa, levels of ATP were measured and found to decline by 40% in 6 h, and this correlated well with transmission electron microscopic evaluation of the tissue (intact superficial cells) [32], In addition, the permeability of a model peptide was unaltered up to 6 h postmortem, but at 8 h, a significant change in permeability was observed [32], These investigators therefore claimed that excised rabbit buccal mucosa could be used for diffusion studies for 6 h. [Pg.101]

Above Tc the first component/Q< (t) relates to the structural relaxation while below Tc it measures the amount of structural arrest. The second part describes fast motional processes (that would take place in the picosecond range, not accessible by NSE) not related to transport phenomena, is the characteristic time of such fast microscopic dynamics. Concerning the structural relaxation, the following predictions are made ... [Pg.113]

A recent development in SPM technology is the combination of SECM and AFM to produce a hybrid high-resolution microscope that allows simultaneous topographic and electrochemical imaging.22 Figure 19 shows an example of this measurement in which pore structure and molecular transport of a redox-active molecule (Ru(NH3)e2+) were simultaneously imaged at l-nm resolution. Inspection of this image clearly shows a correlation between transport rates and pore structure. [Pg.242]

Exploiting the principles of statistical mechanics, atomistic simulations allow for the calculation of macroscopically measurable properties from microscopic interactions. Structural quantities (such as intra- and intermolecular distances) as well as thermodynamic quantities (such as heat capacities) can be obtained. If the statistical sampling is carried out using the technique of molecular dynamics, then dynamic quantities (such as transport coefficients) can be calculated. Since electronic properties are beyond the scope of the method, the atomistic simulation approach is primarily applicable to the thermodynamics half of the standard physical chemistry curriculum. [Pg.210]

A solution of brain lipids was brushed across a small hole in a 5-ml. polyethylene pH cup immersed in an electrolyte solution. As observed under low power magnification, the thick lipid film initially formed exhibited intense interference colors. Finally, after thinning, black spots of poor reflectivity suddenly appeared in the film. The black spots grew rapidly and evenutally extended to the limit of the opening (5, 10). The black membranes have a thickness ranging from 60-90 A. under the electron microscope. Optical and electrical capacitance measurements have also demonstrated that the membrane, when in the final black state, corresponds closely to a bimolecular leaflet structure. Hence, these membranous structures are known as bimolecular, black, or bilayer lipid membranes (abbreviated as BLM). The transverse electrical and transport properties of BLM have been studied usually by forming such a structure interposed between two aqueous phases (10, 17). [Pg.112]

In addition to the change in the theoretical methods applied to hydrates, there have been significant advancements and widespread use of meso- and microscopic tools in hydrate research. Conversely, the typical static experimental apparatus used today to measure macroscopic properties, such as phase equilibria properties, is based on the same principles as the apparatus used by Deaton and Frost (1946). In part, this is due to the fact that the simplest apparatus is both the most elegant and reliable simulation of hydrate formation in industrial systems. In Section 6.1.1 apparatuses for the determination of hydrate thermodynamic and transport macroscopic properties are reviewed. [Pg.319]

We can observe electro-osmosis directly with an optical microscope using liquids, which contain small, yet visible, particles as markers. Most measurements are made in capillaries. An electric field is tangentially applied and the quantity of liquid transported per unit time is measured (Fig. 5.13). Capillaries have typical diameters from 10 fim up to 1 mm. The diameter is thus much larger than the Debye length. Then the flow rate will change only close to a solid-liquid interface. Some Debye lengths away from the boundary, the flow rate is constant. Neglecting the thickness of the electric double layer, the liquid volume V transported per time is... [Pg.75]


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See also in sourсe #XX -- [ Pg.181 ]




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Transport measurements

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