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Displacement steady state

Screw compressors have two rotors with interlocking lobes and act as positive-displacement compressors (see Figure 44.11). This type of compressor is designed for baseload, or steady state, operation and is subject to extreme instability should either the inlet or discharge conditions change. Two helical gears mounted on the outboard ends of the male and female shafts synchronize the two rotor lobes. [Pg.709]

Hydrogen Overpotential (Overvoltage) the displacement of the equilibrium (or steady-state) electrode potential of a cathode required for the discharge of hydrogen ions at a given rate per unit area of electrode. [Pg.1369]

Figure 10.20. A partial alteration in the efficacy of the agonist results in a different steady state whereby the curve is partially depressed but no further dextral displacement is observed (Figure 10.19b and Figure 10.21, see Section 10.6.6). While the models used to describe allosteric alteration of both affinity and efficacy of receptors are complex and require a number of parameters, the identification of such effects (namely, incomplete antagonism of agonist response) is experimentally quite clear and straightforward. Figure 10.20. A partial alteration in the efficacy of the agonist results in a different steady state whereby the curve is partially depressed but no further dextral displacement is observed (Figure 10.19b and Figure 10.21, see Section 10.6.6). While the models used to describe allosteric alteration of both affinity and efficacy of receptors are complex and require a number of parameters, the identification of such effects (namely, incomplete antagonism of agonist response) is experimentally quite clear and straightforward.
The work done in the deformation zone can be estimated assuming the deformation zone propagates together with the crack and maintains its steady state displacement profile [86]... [Pg.343]

Steady-state kinetics. The nickel complex Ni2(C5H5)2(CO)2 reacts with diphenylacety-Iene (dpa) to add dpa and displace both CO molecules. Assume the following mechanism ... [Pg.96]

A capillary system is said to be in a steady-state equilibrium position when the capillary forces are equal to the hydrostatic pressure force (Levich 1962). The heating of the capillary walls leads to a disturbance of the equilibrium and to a displacement of the meniscus, causing the liquid-vapor interface location to change as compared to an unheated wall. This process causes pressure differences due to capillarity and the hydrostatic pressures exiting the flow, which in turn causes the meniscus to return to the initial position. In order to realize the above-mentioned process in a continuous manner it is necessary to carry out continual heat transfer from the capillary walls to the liquid. In this case the position of the interface surface is invariable and the fluid flow is stationary. From the thermodynamical point of view the process in a heated capillary is similar to a process in a heat engine, which transforms heat into mechanical energy. [Pg.351]

The effect of the acceleration due to gravity on the steady-state liquid velocity and the meniscus position is shown in Fig. 10.12. An increase in g is accompanied by the displacement of the meniscus toward the inlet and a decrease in the liquid velocity. [Pg.419]

Figure 13. The Gibbs energy available from a reaction, A B, depends on its displacement from equilibrium when IB)/IA) = K. The AC value is plotted against the mass-action ratio, and this is the value when B1/ A] is maintained constant in the steady state if the rate of substrate supply and substrate removal is constant. Figure 13. The Gibbs energy available from a reaction, A B, depends on its displacement from equilibrium when IB)/IA) = K. The AC value is plotted against the mass-action ratio, and this is the value when B1/ A] is maintained constant in the steady state if the rate of substrate supply and substrate removal is constant.
That the terminal acceleration should most likely vanish is true almost by definition of the steady state the system returns to equilibrium with a constant velocity that is proportional to the initial displacement, and hence the acceleration must be zero. It is stressed that this result only holds in the intermediate regime, for x not too large. Hence and in particular, this constant velocity (linear decrease in displacement with time) is not inconsistent with the exponential return to equilibrium that is conventionally predicted by the Langevin equation, since the present analysis cannot be extrapolated directly beyond the small time regime where the exponential can be approximated by a linear function. [Pg.20]

Droplet suspensions (gas-liquid, two-component system) Since the inertia of a liquid suspended in the gas phase is higher than the inertia of the gas, the time for the displacement of liquid under the pressure waves should be considered. Temkin (1966) proposed a model to account for the response of suspension with pressure and temperature changes by considering the suspensions to move with the pressure waves according to the Stokes s law. The oscillatory state equation is thereby approximated by a steady-state equation with the oscillatory terms neglected, which is valid if the ratio of the relaxation time to the wave period is small, or... [Pg.268]

In the next run, a core pack was saturated with 8.6 cp (at 50° C) Ranger-zone crude oil and water flooded to residual oil saturation. Polymer flood was then initiated and about 1.2% of the original oil in place (OOIP) was recovered. The results are shown in Figure 4. The pressure profiles show behavior essentially similar to the previous run except that the pressure drop across the core increased to 100 psi within 4 PV of injection of polymer. The steady state values of pH and viscosity were 7.0 and 0.7 cp. respectively. The oil ganglia retained in larger pores resisting displacement probably reduced the amount of polymer adsorbed and reduced the number of pores that the polymer molecules needed to seal off in order to block the core. This could explain the more rapid plugging of the core. Effluent pH and viscosities remained much lower than influent values. [Pg.250]

The intermediate reaction complexes (after formation with rate constant, fc,), can undergo unimolecular dissociation ( , ) back to the original reactants, collisional stabilization (ks) via a third body, and intermolecular reaction (kT) to form stable products HC0j(H20)m with the concomitant displacement of water molecules. The experimentally measured rate constant, kexp, can be related to the rate constants of the elementary steps by the following equation, through the use of a steady-state approximation on 0H (H20)nC02 ... [Pg.217]

The solids flux depends on the local concentration of solids, the settling velocity of the solids at this concentration relative to the liquid, and the net velocity of the liquid. Thus the local solids flux will vary within the thickener because the concentration of solids increases with depth and the amount of liquid that is displaced (upward) by the solids decreases as the solids concentration increases, thus affecting the upward drag on the particles. As these two effects act in opposite directions, there will be some point in the thickener at which the actual solids flux is a minimum. This point determines the conditions for stable steady-state operation, as explained below. [Pg.433]

An alternative to derivatizing carbohydrates is the use of indirect photometric detection. In this method, a detectable co-ion in the electrolyte is added to the buffer system generating a steady state absorbance signal in the detector. As the analyte ions migrate in front of the detector window, they displace the detectable co-ion and cause a decrease or negative response in the detector signal. This method provides universal detection of all anions or cations. Since most carbohydrates are not ionized... [Pg.51]

Isotachophoresis. In isotachophoresis (ITP), or displacement electrophoresis or multizonal electrophoresis, the sample is inserted between two different buffers (electrolytes) without electroosmotic flow. The electrolytes are chosen so that one (the leading electrolyte) has a higher mobility and the other (the trailing electrolyte) has a lower mobility than the sample ions. An electric field is applied and the ions start to migrate towards the anode (anions) or cathode (cations). The ions separate into zones (bands) determined by their mobilities, after which each band migrates at a steady-state velocity and steady-state stacking of bands is achieved. Note that in ITP, unlike ZE, there is no electroosmotic flow and cations and anions cannot be separated simultaneously. Reference 26 provides a recent example of capillary isotachophoresis/zone electrophoresis coupled with nanoflow ESI-MS. [Pg.113]

A solution of concentration C0 is pumped at a velocity u through a catalyst bed in which the dispersion, coefficient is D and the rate equation is r = 0.001(C-Ce) where Ce is constant. For a boundary condition, note that C will remain constant as distance z = > a>. Find the reactor lengths z that will reduce the displacement of concentration from the equilibrium value by 50% under steady state conditions when (a) D = 0,2 and u=0.05 (b) D - 0.2 and u = 0 (c) D = 0 and u = 0.05. [Pg.641]

Figure 4. Plot of the full-field solution for the normalized hydrostatic stress Figure 4. Plot of the full-field solution for the normalized hydrostatic stress <Jlk / 3<r0, plastic strain eF, and normalized hydrogen concentrations at steady state vs. normalized distance R lb from the crack tip along the axis of symmetry ahead of the crack tip. The parameters C, and CT are respectively hydrogen concentrations in NILS and trapping sites, and b = 7.13 pm denotes the crack tip opening displacement at 15 MPa.
Figure 6. Normalized NILS hydrogen concentration CL / C at steady state vs. normalized distance R/b from the crack tip for the full-field (crack depth wh=0.2) and MBL (domain size L=h-a) solutions under zero hydrogen flux conditions on the OD surface and remote boundary, respectively. The parameter b denotes the crack tip opening displacement for each case. The inset shows the concentrations near the crack tip. Figure 6. Normalized NILS hydrogen concentration CL / C at steady state vs. normalized distance R/b from the crack tip for the full-field (crack depth wh=0.2) and MBL (domain size L=h-a) solutions under zero hydrogen flux conditions on the OD surface and remote boundary, respectively. The parameter b denotes the crack tip opening displacement for each case. The inset shows the concentrations near the crack tip.

See other pages where Displacement steady state is mentioned: [Pg.261]    [Pg.395]    [Pg.53]    [Pg.53]    [Pg.1136]    [Pg.449]    [Pg.149]    [Pg.187]    [Pg.242]    [Pg.256]    [Pg.773]    [Pg.26]    [Pg.438]    [Pg.45]    [Pg.1219]    [Pg.249]    [Pg.243]    [Pg.154]    [Pg.481]    [Pg.40]    [Pg.94]    [Pg.234]    [Pg.208]    [Pg.192]    [Pg.194]    [Pg.197]    [Pg.597]    [Pg.161]    [Pg.164]    [Pg.229]    [Pg.326]   
See also in sourсe #XX -- [ Pg.81 , Pg.86 ]




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