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Drops transient response

The basic phenomenon was observed in modeling studies by Bjoreskov and Slinko (1965) that sudden increase in inlet temperature caused a transient drop of the peak temperature. The wrong-way response name was given by Mechta et al (1981) after they experienced the opposite a sudden of inlet temperature resulted in an increase of the peak temperature (which may eventually cause a runaway.) The work used a pseudo-homogeneous reaction model and explained the phenomenon by the different speeds of transient response in gas and solid. The example in the last part of Chapter 7.4 explained the speed difference by the large difference in heat capacity of gas and solid phases. For this a two-phase model is needed and spatial and time changes must be followed. [Pg.207]

When 2M methanol solution is fed to the stack at a flow rate of 2 ml/min and the stack is operated at a constant voltage output of 3.8V, the transient response of the stack current density is shown in Fig. 3 varying the flow rate of air to the cathode. The stack was maintained at a temperature of 50°C throughout the experiment. As shown in the figure, while the stack current is maintained at the air flow rates higher than 2 L/min, the stack current begins unstable at the slower flow rates. A similar result is shown in Fig. 4 for varying methanol flow rate at an air flow rate of 2 lymin. At a methanol flow rate of 8 ml/min, the current density reaches initially a current density value of about 130 mA/cm and then starts to decrease probably due to medianol crossover. As the methanol flow rate decreases, the stack current density increases slowly until the methanol flow rate reaches 3 ml/min because of the reduced methanol crossover. The current density drops rapidly from the methanol flow rate of 2 ml/min. [Pg.595]

Figure 4.60 Measured low drop-out regulator transient response. Figure 4.60 Measured low drop-out regulator transient response.
Demonstrate rapid reformer start-up based on low pressure-drop concepts. This reactor design should also provide improved transient response characteristics. [Pg.314]

Transient Response 5s 5 S Further improvements expected with incorporation of low pressure-drop components. [Pg.315]

FIGURE 51.2 Normalized Ar transient response detected by mass spectrometer following He-He/Ar step change. Curves A and C are obtained without proper adjustment of the pressure drop in the feed lines. Curve B corresponds to equal values of pressure drop in the feed Unes. [Pg.1230]

Figure 6.5 shows the transient cell performance behaviors at different current densities and with different toluene inlet concentrations. On the one hand, the effect of toluene contamination becomes more severe with a higher toluene concentration at the same cell current density for example. Figure 6.5(d) indicates that at the same current density of 1.0 Acm, the cell voltage drops due to toluene concentrations of 250, 500, and 750 ppb are 37, 42, and 48 mV, respectively. On the other hand, the toluene contamination increases steadily with increasing cell current density for example, the voltage drops in response to 750 ppb toluene in the cathode flow channel are 9,16, 27, and 48 mV, corresponding to cell current densities of 0.5, 0.75, and 1.0 AcmV respectively, as shown in Figure 6.5. Furthermore, the time required for the cell voltage to reach steady state is also affected by both toluene concentration and current density, i.e., a larger toluene concentration and a lower current density result in a longer time before cell performance reaches steady state. Figure 6.5 shows the transient cell performance behaviors at different current densities and with different toluene inlet concentrations. On the one hand, the effect of toluene contamination becomes more severe with a higher toluene concentration at the same cell current density for example. Figure 6.5(d) indicates that at the same current density of 1.0 Acm, the cell voltage drops due to toluene concentrations of 250, 500, and 750 ppb are 37, 42, and 48 mV, respectively. On the other hand, the toluene contamination increases steadily with increasing cell current density for example, the voltage drops in response to 750 ppb toluene in the cathode flow channel are 9,16, 27, and 48 mV, corresponding to cell current densities of 0.5, 0.75, and 1.0 AcmV respectively, as shown in Figure 6.5. Furthermore, the time required for the cell voltage to reach steady state is also affected by both toluene concentration and current density, i.e., a larger toluene concentration and a lower current density result in a longer time before cell performance reaches steady state.
Special opportunities for the industrial implementation of structured catalysts are offered by the growing interest in millisecond contact time processes, in view of the associated requirements on pressure drop and flow distribution to be matched with strict size constraints. In this case, a better control of the complex interplay between heat and mass transfer and heterogeneous/homogeneous reactions granted by structured catalysts would provide guidelines for the design of reactors and processes with optimized performances in terms of selectivity, yield, fast transient response and operational flexibility. [Pg.990]

Transient kinetic phenomena of another type were observed in the so-called purging experiments, whereby we switched from feeding the flow reactor with a helium-butyl alcohol mixture to one with pure helium and then back to the previous helium-butyl alcohol. A typical response of a catalyst to such purging is given in Fig. 6, referring to the dehydration of sec- and isobutyl alcohols over HZSM-5. For sec-butyl alcohol, the rate of butene formation initially increases by a factor of about 10 upon purging and then drops to zero. Return (8k) to the... [Pg.343]

An important test of a transient spectrometer s accuracy, stability, and noise level is provided by a baseline spectrum. This is an averaged spectrum obtained in exactly the same way as actual data, except that the ultraviolet excitation beam is kept blocked when it would otherwise be open. The lowest trace shown in Figure 2 is a typical 5-cycle baseline spectrum for our system. Systematic deviation from zero is less than 0. 01 absorbance units throughout, and the r. m. s. noise level varies from 0. 03 near the edges to 0. 007 near the center of the spectrum. These noise variations are inversely related to the detected single beam intensity spectrum, which drops on the blue side because of the continuum distribution and the transmissive properties of our beam combiner, and on the red side because of the photocathode response of the SIT detector head. A high degree of intensity linearity in the OMA is necessary for our... [Pg.231]

Acetylcholineesterase Bilayer lipid membranes were prepared by adding a solution of egg phosphatidylcholine and dipalmi-toyl phosphatidic acid dropwise into the surface of aqueous 0.1 M KC1/10 mM HEPES, near the Saran Wrap partition of a two compartment plexiglass cell. A portion of AChE solution in 10 mM Tris hydrochloride buffer solution of pH 7.4 was applied. The electrolyte level was momentarily dropped below the orifice and raised to form a membrane. The membranes were used as transducers for the reaction of AChE with ACh. An external voltage (25 mV) was applied across the membrane between two Ag/AgCl reference electrodes. Enzymatically generated hydronium ion causes transient current due to alteration of the electrostatic field by the ionization of dipalmitoyl phosphatidic acid. The response delay time was directly related to the substrate concentration where acetylcholine can be determined from 1 pM upto mM level. [113]... [Pg.56]

Figure 5 represents an ideal reversible one-electron transfer process in the absence of drop or capacitative charging current, although in real experiments contributions to the response from both these terms are unavoidable. Figure 6 shows the effect of uncompensated resistance for both transient and steady-state voltammograms, whilst Fig. 7 shows the influence of double layer capacitance on a cyclic voltammetric wave. Note that for steady-state voltammetric techniques only very low capacitative charging... [Pg.14]


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See also in sourсe #XX -- [ Pg.542 ]




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