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Parallel-band apparatus

Taylor describes experiments with rf jr] having values of0.0003, 0.5, 0.9, and 20. He observed that, in the parallel-band apparatus that produced a shearing flow, when (t] /rf) is 0.0003 (i.e., a very low viscosity drop is placed in a high-viscosity matrix) the drop is elongated indefinitely in flow. However, (L—B)/ L+B) increases less rapidly than Tjay/K, unlike the expectation from Eq. (6.28b). In the four-roller elongational flow apparatus, the deformation of the drop (I—B)/(I + B) was a unique function of tjaE/K and obeyed Eq. (6.28b) at low stretch rates. At higher stretch rates (I—B)/(I+ B) increases less rapidly. The results were quantitatively similar to the shear flow behavior. [Pg.278]

When rf jt] was 0.5, the drop in the parallel-band apparatus elongated into a threadlike form. The deformation of the droplet was related to y at low shear rates through Eq. (6.29b). When L—B)/ L+B) reached 0.8, the drop burst. This was at a value of rjay/K of 1.5. [Pg.278]

A study of the effect of gap thickness on band formation in HPC + water solutions was conducted [87]. The apparatus used had a parallelism of about 20 pm over a plate length of about 10 cm. Note that this was a linear and not a rotary parallel plate apparatus. The gap was varied between 150 and 1000 pm. A rest time of 5-6 h was allowed between sample loading and initiation of shear. Since the time scale of changes in the band structure was slow, of the order of minutes, there was plenty of time for detailed examination. [Pg.389]

The setup used for crossed beam experiments is basically the same apparatus used in the H2O photodissociation studies but slightly modified. In the crossed beam study of the 0(1D) + H2 — OH + H reaction and the H + HD(D2) — H2(HD) + D reaction, two parallel molecular beams (H2 and O2) were generated with similar pulsed valves. The 0(1D) atom beam was produced by the 157 photodissociation of the O2 molecule through the Schumann-Runge band. The 0(1D) beam was then crossed at 90° with the... [Pg.94]

Of course, this value is difficult to obtain experimentally because of the band path width limitation of the measurement apparatus. The IEC 62391 standard defines the method used to measure the series resistance. The self-discharge due either to the leakage current or to the charge redistribution adds a contribution to the voltage drop corresponding to Rp, the parallel resistance in the model. [Pg.437]

As discussed by Weber et al. (1978), the same mechanism appears to have operated in experiments performed by Mandl et al. (1977), during which continuous clay smears were produced in a ring-shear apparatus by extruding material from a sheared-off clay band. In these experiments, the much smaller difference between the fault-parallel and the fault-normal stress within the plastic clay, as compared with that in the sand, must have caused the observed extrusion. [Pg.44]

The excellent resolution achieved by electrofocusing is retained. (2) The time between stop of run and fixation of the gel is so short that the difference between adjacent bands is not disturbed. This sometimes happens with the sucrose gradient technique. (3) The apparatus and technique are very simple. (4) Several samples can be treated in parallel when using the thin layer type apparatus. (5) The amounts of Ampholine... [Pg.64]

Fig. 5. A schematic illustration of an angle-resolved photoemission experiment An incident photon, with wavevector p and polarization E, strikes the sample with polar incidence angles (61p, p) relative to the crystal axes. In practice the light source is generally fixed relative to either the crystal or the detector. However, the ability to vary the photon polarization from synchrotron sources provides a powerful tool for obtaining information on the symmetries of electronic states. By moving the analyzer or the sample (depending on the details of the experimental apparatus), photoelectrons leaving the surface at polar angles (6, ) are collected by the spectrometer the component of their crystal momentum, k, parallel to the sample surface is strictly conserved, allowing accurate determination of the two-dimensional band structure. Fig. 5. A schematic illustration of an angle-resolved photoemission experiment An incident photon, with wavevector p and polarization E, strikes the sample with polar incidence angles (61p, p) relative to the crystal axes. In practice the light source is generally fixed relative to either the crystal or the detector. However, the ability to vary the photon polarization from synchrotron sources provides a powerful tool for obtaining information on the symmetries of electronic states. By moving the analyzer or the sample (depending on the details of the experimental apparatus), photoelectrons leaving the surface at polar angles (6, ) are collected by the spectrometer the component of their crystal momentum, k, parallel to the sample surface is strictly conserved, allowing accurate determination of the two-dimensional band structure.
The apparatus with parallel white bands imagined by Savart alters, for the eye of the observer, vertical dimensions of the bulges and the isolated masses, and can-... [Pg.381]


See other pages where Parallel-band apparatus is mentioned: [Pg.277]    [Pg.277]    [Pg.390]    [Pg.150]    [Pg.555]    [Pg.1215]    [Pg.568]    [Pg.12]    [Pg.373]    [Pg.3]    [Pg.367]    [Pg.213]    [Pg.492]    [Pg.17]    [Pg.186]   
See also in sourсe #XX -- [ Pg.277 ]




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