Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Constitutive quantity

Let = pf,c,p = grade, Fs, (3f,d = grad 0f,Us, T = grad Us be the array of fields describing the elastic state of our isothermal process and, in addition, let us enclose the relative velocity u and the solid one vH by imposing the principle of equipresence, we postulate that constitutive quantities Th, Ki, Ct, Si, m, M and a are all twice continuously differentiable functions with respect to all constitutive fields and require the consistency with the in-... [Pg.188]

The notion of state was derived from the theory of mechanics and of thermodynamics and generalised by mathematical system theory. Following the tradition of the field theory of continua (Truesdell Noll, 1965) quantities of a theory can be classified into two categories state variables and constitutive quantities. State variables are functions such that their values... [Pg.16]

According to the conventional treatment of pure homogeneous reaction kinetics the state is a finite-dimensional vector and the only constitutive quantities are the reaction rates. [Pg.17]

The theory of thermomechanics adopts the concept of materials with memory . According to this concept the constitutive quantities depend on the history of the independent variables, and not only on their actual value. In other words, it is not definite that the instantaneous value of state variables (i.e. the state) completely determines the state. [Pg.17]

Please note the identity between the velocity v and the time derivative of u. Furthermore the quantities f, a, q and r stand for the sum of externally applied body forces, the transposed Cauchy stress tensor, the heat flux, and an arbitrary energy production term (e.g. due to latent heat during phase transitions). Eqs. (1-3) are equations of motion for the five unknown fields p, u and e. They are universal, namely material-independent. To solve these equations, the constitutive quantities, viz. heat flux and stress tensor, must be replaced by constitutive equations (cf. subsequent paragraph) q = (T, VT,...) and = (T,u,...). Moreover, up to now no temperature T occur in the balances (1-3). For this reason a caloric state equation, e = e T), must be introduced, which allows for replacing the internal energy e by temperature T. [Pg.77]

These equations involve the constitutive quantities ty qk s and e (where fk and... [Pg.25]

It is true that the equations of balance (3.8)-(3.13) are not useful in their present form, even if, as we shall assume, fj and Z are given fields. Indeed, these balance laws join the constitutive quantities ty s e q and h to the... [Pg.30]

The relation between the Langevin equations (3.49) [assuming -correlated gaussian random forces obeying (3.59, 61)] and the stochastic equation (3.29) has now to be established. The constitutive quantities of the latter equation are the moments, see (3.23, 28),... [Pg.69]

Simple conventional refining is based essentially on atmospheric distillation. The residue from the distillation constitutes heavy fuel, the quantity and qualities of which are mainly determined by the crude feedstock available without many ways to improve it. Manufacture of products like asphalt and lubricant bases requires supplementary operations, in particular separation operations and is possible only with a relatively narrow selection of crudes (crudes for lube oils, crudes for asphalts). The distillates are not normally directly usable processing must be done to improve them, either mild treatment such as hydrodesulfurization of middle distillates at low pressure, or deep treatment usually with partial conversion such as catalytic reforming. The conventional refinery thereby has rather limited flexibility and makes products the quality of which is closely linked to the nature of the crude oil used. [Pg.484]

A general prerequisite for the existence of a stable interface between two phases is that the free energy of formation of the interface be positive were it negative or zero, fluctuations would lead to complete dispersion of one phase in another. As implied, thermodynamics constitutes an important discipline within the general subject. It is one in which surface area joins the usual extensive quantities of mass and volume and in which surface tension and surface composition join the usual intensive quantities of pressure, temperature, and bulk composition. The thermodynamic functions of free energy, enthalpy and entropy can be defined for an interface as well as for a bulk portion of matter. Chapters II and ni are based on a rich history of thermodynamic studies of the liquid interface. The phase behavior of liquid films enters in Chapter IV, and the electrical potential and charge are added as thermodynamic variables in Chapter V. [Pg.1]

Generally speaking, intermolecular forces act over a short range. Were this not the case, the specific energy of a portion of matter would depend on its size quantities such as molar enthalpies of formation would be extensive variables On the other hand, the cumulative effects of these forces between macroscopic bodies extend over a rather long range and the discussion of such situations constitutes the chief subject of this chapter. [Pg.225]

Both disadvantages of the Buchner funnel are overcome in the Mini -filter this constitutes an important development for the filtration of relatively large quantities of materials. The upper portion, carrying a... [Pg.134]

The quantity, V(R), the sum of the electronic energy Egjg. computed in a wave function calculation and the nuclear-nuclear coulomb interaction V(R,R), constitutes a potential energy surface having 3N independent variables (the coordinates R). The independent variables are the coordinates of the nuclei but having made the Born-Oppenheimer approximation, we can think of them as the coordinates of the atoms in a molecule. [Pg.164]

Conformity to the Langmuir equation, where it occurs, does not constitute proof of the correctness of the mechanism, since both B (or c) and n are disposable constants the quantities v, and , (cf. Equation... [Pg.199]

As with the rate of polymerization, we see from Eq. (6.37) that the kinetic chain length depends on the monomer and initiator concentrations and on the constants for the three different kinds of kinetic processes that constitute the mechanism. When the initial monomer and initiator concentrations are used, Eq. (6.37) describes the initial polymer formed. The initial degree of polymerization is a measurable quantity, so Eq. (6.37) provides a second functional relationship, different from Eq. (6.26), between experimentally available quantities-n, [M], and [1]-and theoretically important parameters—kp, k, and k. Note that the mode of termination which establishes the connection between u and hj, and the value of f are both accessible through end group characterization. Thus we have a second equation with three unknowns one more and the evaluation of the individual kinetic constants from experimental results will be feasible. [Pg.370]

Apatite and other phosphorites constitute a substantial resource of rare earths. The REO content is highly variable and ranges from trace amounts to over 1%. Apatite- [1306-05-4] rich tailings of the iron ore at Mineville, New York, have been considered a potential source of yttrium and lanthanides. Rare-earth-rich apatites are found at the Kola Peninsula, Russia, and the Phalaborwa complex in South Africa. In spite of low REO content apatites could become an important source of rare earths because these are processed in large quantities for the manufacturing of fertilisers (qv). [Pg.543]

Shale oil contains large quantities of olefinic hydrocarbons (see Table 8), which cause gumming and constitute an increased hydrogen requirement for upgrading. Properties for cmde shale oil are compared with petroleum cmde in Table 10. High pour points prevent pipeline transportation of the cmde shale oil (see Pipelines). Arsenic and iron can cause catalyst poisoning. [Pg.353]

Polyall lene Oxide Block Copolymers. The higher alkylene oxides derived from propjiene, butylene, styrene (qv), and cyclohexene react with active oxygens in a manner analogous to the reaction of ethylene oxide. Because the hydrophilic oxygen constitutes a smaller proportion of these molecules, the net effect is that the oxides, unlike ethylene oxide, are hydrophobic. The higher oxides are not used commercially as surfactant raw materials except for minor quantities that are employed as chain terminators in polyoxyethylene surfactants to lower the foaming tendency. The hydrophobic nature of propylene oxide units, —CH(CH2)CH20—, has been utilized in several ways in the manufacture of surfactants. Manufacture, properties, and uses of poly(oxyethylene- (9-oxypropylene) have been reviewed (98). [Pg.254]

Terphenyls in heat-transfer appHcations are used in relatively smaller quantities with negligible release to the environment. They are sufficiently biodegradable so as not to constitute an environmental threat (56,57). Some properties important for environmental considerations are summari2ed in Table 7. [Pg.118]

The economic importance of copolymers can be cleady illustrated by a comparison of U.S. production of various homopolymer and copolymer elastomers and resins (102). Figure 5 shows the relative contribution of elastomeric copolymers (SBR, ethylene—propylene, nitrile mbber) and elastomeric homopolymers (polybutadiene, polyisoprene) to the total production of synthetic elastomers. Clearly, SBR, a random copolymer, constitutes the bulk of the entire U.S. production. Copolymers of ethylene and propylene, and nitrile mbber (a random copolymer of butadiene and acrylonitrile) are manufactured in smaller quantities. Nevertheless, the latter copolymers approach the volume of elastomeric butadiene homopolymers. [Pg.187]

Generally, a few harmonic quantities are always present in an a.c. system, as normally some non-linear loads always constitute a power system. These harmonics may not affect the operation of the inductive loads connected on the system as much as a capacitive load or a communication network that may be running in parallel or in the vicinity of such a power system. [Pg.732]

Another generalization uses referential (material) symmetric Piola-Kirchhoff stress and Green strain tensors in place of the stress and strain tensors used in the small deformation theory. These tensors have components relative to a fixed reference configuration, and the theory of Section 5.2 carries over intact when small deformation quantities are replaced by their referential counterparts. The referential formulation has the advantage that tensor components do not change with relative rotation between the coordinate frame and the material, and it is relatively easy to construct specific constitutive functions for specific materials, even when they are anisotropic. [Pg.119]

As with any constitutive theory, the particular forms of the constitutive functions must be constructed, and their parameters (material properties) must be evaluated for the particular materials whose response is to be predicted. In principle, they are to be evaluated from experimental data. Even when experimental data are available, it is often difficult to determine the functional forms of the constitutive functions, because data may be sparse or unavailable in important portions of the parameter space of interest. Micromechanical models of material deformation may be helpful in suggesting functional forms. Internal state variables are particularly useful in this regard, since they may often be connected directly to averages of micromechanical quantities. Often, forms of the constitutive functions are chosen for their mathematical or computational simplicity. When deformations are large, extrapolation of functions borrowed from small deformation theories can produce surprising and sometimes unfortunate results, due to the strong nonlinearities inherent in the kinematics of large deformations. The construction of adequate constitutive functions and their evaluation for particular... [Pg.120]

The state variables define a point on the diagram the "constitution point". If this point is given, then the equilibrium number of phases can be read off. So, too, can their composition and the quantity of each phase - but that comes later. So the diagram tells you the entire constitution of any given alloy, at equilibrium. Refer back to the definition of eonstitution (p. 311) and check that this is so. [Pg.327]


See other pages where Constitutive quantity is mentioned: [Pg.87]    [Pg.7]    [Pg.17]    [Pg.17]    [Pg.18]    [Pg.277]    [Pg.277]    [Pg.177]    [Pg.31]    [Pg.87]    [Pg.7]    [Pg.17]    [Pg.17]    [Pg.18]    [Pg.277]    [Pg.277]    [Pg.177]    [Pg.31]    [Pg.321]    [Pg.102]    [Pg.725]    [Pg.378]    [Pg.394]    [Pg.287]    [Pg.469]    [Pg.481]    [Pg.258]    [Pg.260]    [Pg.498]    [Pg.295]    [Pg.384]    [Pg.367]    [Pg.80]    [Pg.2052]    [Pg.217]   
See also in sourсe #XX -- [ Pg.7 , Pg.16 , Pg.17 , Pg.18 ]




SEARCH



© 2024 chempedia.info