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Exactly specified system

Now let us consider the wine-making example and ask, Can we control temperature to produce a product of any exactly specified alcohol content (up to, say, 12%) The answer is that we probably cannot, and the reason is that the system behavior is initially not known with certainty. We know that some transform relating the alcohol content to the important factors must exist - that is. [Pg.13]

The photoinduced electron transfer (PET) is especially important in the case of large or giant molecules (supermolecules), ie systems made up of molecular components in the same way as molecules are made up of atoms [11-19], As the systems are made up of a number of discrete components held together by different but not always exactly specified forces (covalent bonds, electrostatic interactions, hydrogen bonds, or other intermolecular interactions), the photoinduced electron transfer or energy transfer in these systems may be formally treated as intermolecular [20],... [Pg.44]

Suppose you have a closed vessel containing three components A, B, and C distributed between gas and liquid phases, and you wish to describe this system to someone else in sufficient detail for that person to duplicate it exactly. Specifying the system temperature and pressure, the masses of each phase, and two mass or mole fractions for each phase would certainly be sufficient however, these variables are not all independent—once some of them are specified, others are fixed by nature and, in some cases, may be calculated from physical properties of the system components. [Pg.247]

Case 1. If / = 0, we have a system of equations with equal number of variables. The solution of the E equations yields unique values for the V variables. In this case we say that the process is exactly specified. [Pg.54]

To eliminate conflict (a) we can delete the feedforward flow control loop in the coolant system. To erase conflict (b) we delete the flow control loop in the flash drum. Thus the final control configuration for the overall process is shown in Figure 23.6b. It has no conflicts among the loops and the process is exactly specified. [Pg.248]

Library systems designed to retrieve references identical to the query are called identity search systems. Since the identity of any object (spectrum, chromatogram, chemical structure, set of chemical features) is well defined, the identity search is reduced to the binary decision identical/not identical. The system has to be insensitive to varying instrumental conditions, but there is no need to discriminate between different degrees of similarity. The identity search system is useful only in a limited range of applications for example, in the field of environmental control or drug control where the set of compounds that are expected or have to be identified are exactly specified. Any other, unspecified compound is irrelevant. In most other applications the unexpected compounds are of prime interest, so that the identity search is of limited use. [Pg.4547]

Because the two outputs are the only variables to be determined in solving the system of two equations, no degrees of freedom are left. The system of equations is exactly specified and hence solvable. [Pg.21]

Corrosion-control systems exactly specified and the conditions of their application stated... [Pg.378]

One may now consider how changes can be made in a system across an adiabatic wall. The first law of thermodynamics can now be stated as another generalization of experimental observation, but in an unfamiliar form the M/ork required to transform an adiabatic (thermally insulated) system, from a completely specified initial state to a completely specifiedfinal state is independent of the source of the work (mechanical, electrical, etc.) and independent of the nature of the adiabatic path. This is exactly what Joule observed the same amount of work, mechanical or electrical, was always required to bring an adiabatically enclosed volume of water from one temperature 0 to another 02. [Pg.329]

The slopes of the fimctions shown provide the reaction rates according to the various definitions under the reaction conditions specified in the figure caption. These slopes are similar, but not identical (nor exactly proportional), in this simple case. In more complex cases, such as oscillatory reactions (chapter A3.14 and chapter C3.6). the simple definition of an overall rate law tluough equation (A3.4.6) loses its usefiilness, whereas equation (A3.4.1) could still be used for an isolated system. [Pg.761]

The second approximation in HF calculations is due to the fact that the wave function must be described by some mathematical function, which is known exactly for only a few one-electron systems. The functions used most often are linear combinations of Gaussian-type orbitals exp(—nr ), abbreviated GTO. The wave function is formed from linear combinations of atomic orbitals or, stated more correctly, from linear combinations of basis functions. Because of this approximation, most HF calculations give a computed energy greater than the Hartree-Fock limit. The exact set of basis functions used is often specified by an abbreviation, such as STO—3G or 6—311++g. Basis sets are discussed further in Chapters 10 and 28. [Pg.19]

From the definition of a partial molar quantity and some thermodynamic substitutions involving exact differentials, it is possible to derive the simple, yet powerful, Duhem data testing relation (2,3,18). Stated in words, the Duhem equation is a mole-fraction-weighted summation of the partial derivatives of a set of partial molar quantities, with respect to the composition of one of the components (2,3). For example, in an / -component system, there are n partial molar quantities, Af, representing any extensive molar property. At a specified temperature and pressure, only n — 1) of these properties are independent. Many experiments, however, measure quantities for every chemical in a multicomponent system. It is this redundance in reported data that makes thermodynamic consistency tests possible. [Pg.236]

The general XT E problem involves a multicomponent system of N constituent species for which the independent variables are T, P, N — 1 liquid-phase mole fractions, and N — 1 vapor-phase mole fractions. (Note that Xi = 1 and y = 1, where x, and y, represent liquid and vapor mole fractions respectively.) Thus there are 2N independent variables, and application of the phase rule shows that exactly N of these variables must be fixed to estabhsh the intensive state of the system. This means that once N variables have been specified, the remaining N variables can be determined by siiTUiltaneous solution of the N equihbrium relations ... [Pg.535]

If the regulatoiy control system were perfect, the target could be set exactly equal to the constraint (that is, the target for the pressure controller could be set at the vessel rehef pressure). However, no regulatory control svstem is perfect. Therefore, the value specified for the target must te on the safe side of the constraint, thus giving the control system some elbow room. How much depends on the following ... [Pg.730]

While these different pohcies vaiy broadly in form, their objective is essentially the same to substitute flexible economic-incentive systems for the current rigid, technology-based regulations that specify exactly how companies must comply. These market mechanisms have made regiilating easier for EPA and less burdensome and costly for industiy. [Pg.2158]

It is often assumed that TA cannot be applied during design, because until the plant has been fabricated the tasks to be performed by workers cannot be defined in sufficient detail. In fact, many TA techniques can be used to specify the nature of the tasks to achieve the required process plant functions, even before the exact configuration of the system has been finalized. This point will be elaborated later in the context of hierarchical task analysis. [Pg.161]

Exact performance can be given only by the manufacturer for a specified turbine selected to operate at a particular set of conditions. However, estimates can be made which are usually quite satisfactory for general evaluations and comparisons. The most useful criteria are the steam rate and the system cost. Steam rate is the flow of steam in pounds per brake horsepower output per hour through the turbine. It is established for a definite shaft horsepower output, given steam pressure and temperature, exhaust system pressure, and shaft rpm ... [Pg.672]

Standard V-belt pulleys are specified with exact dimensions as opposed to nominal. The industry adopted the datum system in 1988 as the standard for specifying classic V-belt pulleys. Therefore, all pulley specifications should be in datum dimensions rather than pitch. Individual pulley dimensions are shown in Figure 58.2. [Pg.972]

Newtonian inochaiiics. Since it is impossible to completely specify the initial state of such a system, kinetic theory (contents itself with describing a smoothed version of the system. The smoothed version is simply one whore all exact state-information below some characteristic length and time is replaced by a probabilistic description. [Pg.476]

As we have seen before, exact differentials correspond to the total differential of a state function, while inexact differentials are associated with quantities that are not state functions, but are path-dependent. Caratheodory proved a purely mathematical theorem, with no reference to physical systems, that establishes the condition for the existence of an integrating denominator for differential expressions of the form of equation (2.44). Called the Caratheodory theorem, it asserts that an integrating denominator exists for Pfaffian differentials, Sq, when there exist final states specified by ( V, ... x )j that are inaccessible from some initial state (.vj,.... v )in by a path for which Sq = 0. Such paths are called solution curves of the differential expression The connection from the purely mathematical realm to thermodynamic systems is established by recognizing that we can express the differential expressions for heat transfer during a reversible thermodynamic process, 6qrey as Pfaffian differentials of the form given by equation (2.44). Then, solution curves (for which Sqrev = 0) correspond to reversible adiabatic processes in which no heat is absorbed or released. [Pg.67]


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See also in sourсe #XX -- [ Pg.575 ]




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