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Available energy destruction

The system s Second Law efficiency rises as the work/heat ratio increases (Figure 7). This is partially due to improved performance of the turbine, pump, and condenser and the higher temperature steam from the boiler. This considerably decreases the available-energy destruction due to heat transfer in the boiler. Thus, the turbine can take advantage of this for the production of shaft work. [Pg.279]

This paper provides a framework for the application of Second Law based design methodology to separation systems. A relationship is derived for the available-energy destruction in a binary separation column as a function of the reflux ratio and the feed and product mass fractions. This derivation is limited to separations in which the entropy production is predominately due to mass transfers. [Pg.289]

The results presented In Table III show that as the capital Investment in the tower (Ztower) increases at larger tower heights, the available-energy destruction decreases. Thus the optimal design reflects the classical trade-off between capital investment and fuel cost. It is important to note that heat exchanger design plays a major role in separation systems (16). [Pg.303]

When the transport rates of independent commodities are known (given or determined from kinetic relations), then the available energy transport terms can be evaluated using the aforementioned relations. (The application of these transport relations, which will now be set forth, requires the use of the thermostatic property relations.) Once the transport term values are known, the balance can be used to evaluate the available energy destruction, Aj. [Pg.19]

This artifice avoids the calculation of the available energy loss at the stack exit. Then, the total available energy destruction with the system will include that loss—inasmuch as the lost available energy is ultimately consumed (destroyed) by the dispersion process. [Pg.27]

Available Energy Destruction and Entropy Production. The Second Law of Thermodynamics can be stated to decree that the system available energy of an isolated system decreases in all real processes.. Since E(t) is constant for an isolated system it follows that Ef(t) > 0. [Pg.78]

The available-energy destruction due to friction is computed from the relation (7)... [Pg.178]

An available energy analysis of this problem consists of first evaluating the rates of available energy destruction for the two systems. Using the notation of Figure 1, the same available energy balance cam be written for both A and B ... [Pg.190]

Figure 2. Simple distillation system for the separation of a 45%-55% benzene-toluene feed into 92% benzene distillate and a 95% toluene bottoms product. Available-energy flows and destructions are given in 10° Btu/hr. Figure 2. Simple distillation system for the separation of a 45%-55% benzene-toluene feed into 92% benzene distillate and a 95% toluene bottoms product. Available-energy flows and destructions are given in 10° Btu/hr.
As the impact of fuel cost on product cost continues to increase, so will the desirability of using available energy analysis in optimization of process designs. Efforts over recent years have resulted in many simplified methods for evaluating transports and destructions of available energy, which can be adapted for use on computers or programmable calculators. It is hoped that, with the removal of economic and theoretical barriers, second law... [Pg.35]

It can also be shown (2J that the subsystem available energy changes as a result of transports and/or destructions of subsystem available energy i.e. [Pg.84]

A summary of the destructions of available energy in the system is presented in Table II. An available energy consumption analysis lends itself to this method of presenting results since comparison of corresponding consumptions may be done at a glance. [Pg.192]

The problem of explosion of a vapor cloud is not only that it is potentially very destructive but also that it may occur some distance from the point of vapor release and may thus threaten a considerable area. If the explosion occurs in an unconfined vapor cloud, the energy in the blast wave is generally only a small fraction of the energy theoretically available from the combustion of all the material that constitutes the cloud. The ratio of the actual energy released to that theoretically available from the heat of combustion is referred to as the explosion efficiency. Explosion efficiencies are typically in the range of 1 to 10 percent. A value of 3 percent is often assumed. [Pg.258]

There are numerous techniques which provide information related to the surface energy of solids. A large array of high-vacuum, destructive and non-destructive techniques is available, and most of them yield information on the atomic and chemical composition of the surface and layers just beneath it. These are reviewed elsewhere [83,84] and are beyond the scope of the present chapter. From the standpoint of their effect on wettability and adhesion, the property of greatest importance appears to be the Lifshitz-van der Waals ( dispersion) surface energy, ys. This may be measured by the simple but elegant technique of... [Pg.34]

It follows from the above that the mechanism for electrical potential oscillation across the octanol membrane in the presence of SDS would most likely be as follows dodecyl sulfate ions diffuse into the octanol phase (State I). Ethanol in phase w2 must be available for the transfer energy of DS ions from phase w2 to phase o to decrease and thus, facilitates the transfer of DS ions across this interface. DS ions reach interface o/wl (State II) and are adsorbed on it. When surfactant concentration at the interface reaches a critical value, a surfactant layer is formed at the interface (State III), whereupon, potential at interface o/wl suddenly shifts to more negative values, corresponding to the lower potential of oscillation. With change in interfacial tension of the interface, the transfer and adsorption of surfactant ions is facilitated, with consequent fluctuation in interface o/ wl and convection of phases o and wl (State IV). Surfactant concentration at this interface consequently decreased. Potential at interface o/wl thus takes on more positive values, corresponding to the upper potential of oscillation. Potential oscillation is induced by the repetitive formation and destruction of the DS ion layer adsorbed on interface o/wl (States III and IV). This mechanism should also be applicable to oscillation with CTAB. Potential oscillation across the octanol membrane with CTAB is induced by the repetitive formation and destruction of the cetyltrimethylammonium ion layer adsorbed on interface o/wl. Potential oscillation is induced at interface o/wl and thus drugs were previously added to phase wl so as to cause changes in oscillation mode in the present study. [Pg.711]

This non-destructive technique is a very suitable tool for rapid in-line analysis of inorganic additives in food products (Price and Major, 1990 Anon, 1995). It can be readily used by non-skilled operators, and dry materials can be pressed into a pellet or simply poured into a sample cup. The principles of this technique related to food analysis are described by Pomeranz and Meloan (1994). A useful Internet site is http //www.xraysite.com, which includes information about different XRF instruments from various companies. Wavelength dispersive X-ray fluorescence (WD-XRF) or bench-top energy dispersive (ED-XRF) instruments are available. XRF is a comparative technique, thus a calibration curve needs to be established using food products of the same type as those to be... [Pg.129]


See other pages where Available energy destruction is mentioned: [Pg.264]    [Pg.297]    [Pg.300]    [Pg.180]    [Pg.183]    [Pg.190]    [Pg.264]    [Pg.297]    [Pg.300]    [Pg.180]    [Pg.183]    [Pg.190]    [Pg.307]    [Pg.631]    [Pg.19]    [Pg.31]    [Pg.31]    [Pg.144]    [Pg.178]    [Pg.593]    [Pg.365]    [Pg.188]    [Pg.361]    [Pg.796]    [Pg.797]    [Pg.798]    [Pg.675]    [Pg.208]    [Pg.371]    [Pg.116]    [Pg.85]    [Pg.204]    [Pg.283]    [Pg.311]    [Pg.92]    [Pg.541]    [Pg.3]    [Pg.216]   


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Energy availability

Energy available

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