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Basic equations

A general equation for the heat transport in the solid (carbon) phase of the CCL is [Pg.359]

kr is the CCL thermal conductivity and Rreac is the volumetric rate of electrochemical conversion (A cm ). Equation 4.282 says that the variation of conductive heat flux (the left-hand side) equals the sum of the heating rates from the reaction and the Joule dissipation of electric energy. On the other hand, determines the rate of proton current decay along x  [Pg.359]

The right-hand side of Equation 4.282 includes the dominant sources of heat in catalyst layers of low-temperature fuel cells. Note that part of the heat flux from the CCL is transported with liquid water produced in the ORR. Being not represented explicitly, this flux is taken into account in the equations of this section (see below). [Pg.359]

Generally, evaporation of liquid water is an important mechanism of fuel cell cooling and the evaporation term should be added to the right-hand side of Equation 4.282. For simplicity, in this section, evaporation will be ignored, which is equivalent to the assumption that the water vapor pressure in the CCL is equal to the saturated pressure. Thus, solution to Equation 4.282 gives a maximal heat flux from the CCL, which is of large interest for cell and stack modeling. [Pg.359]

The exact solution to Equation 4.282 is rather cumbersome (Kulikovsky, 2007) however, this equation can be simplified. The temperature variation across the CCL is not large thus, T(x) on the right-hand side may safely be replaced by the temperature at the CCL/GDL interface Ti = T Icl)- [Pg.359]


Equation 11-3 is a special case of a more general relationship that is the basic equation of capillarity and was given in 1805 by Young [1] and by Laplace [2]. In general, it is necessary to invoke two radii of curvature to describe a curved surface these are equal for a sphere, but not necessarily otherwise. A small section of an arbitrarily curved surface is shown in Fig. II-3. The two radii of curvature, R and / 2[Pg.6]

The mathematical theory is rather complex because it involves subjecting the basic equations of motion to the special boundary conditions of a surface that may possess viscoelasticity. An element of fluid can generally be held to satisfy two kinds of conservation equations. First, by conservation of mass. [Pg.121]

A. Thermodynamics of the Electrocapillary Effect The basic equations of electrocapillarity are the Lippmann equation [110]... [Pg.195]

In 1872, Boltzmaim introduced the basic equation of transport theory for dilute gases. His equation detemiines the time-dependent position and velocity distribution fiinction for the molecules in a dilute gas, which we have denoted by /(r,v,0- Here we present his derivation and some of its major consequences, particularly the so-called //-tlieorem, which shows the consistency of the Boltzmann equation with the irreversible fomi of the second law of themiodynamics. We also briefly discuss some of the famous debates surrounding the mechanical foundations of this equation. [Pg.676]

The processes siumnarized by equation ( A3.13.il can follow quite different mechanisms and it is usefiil to classify them and introduce the appropriate nomenclature as well as the basic equations. [Pg.1046]

This is the basic equation for monodisperse particles in light scattering experiments. We can derive tln-ee relationships by extrapolation. [Pg.1393]

The basic equation [8] is tlie equation of motion for the density matrix, p, given in equation (B2.4.25), in which H is the Hamiltonian. [Pg.2099]

This basic equation describes waves, whose properties are related as follows ... [Pg.2855]

Real and imaginary parts of this yield the basic equations for the functions appearing in Eqs. (9) and (10). (The choice of the upper sign in these equations will be justified in a later subsection for the ground-state component in several physical situations. In some other circumstances, such as for excited states in certain systems, the lower sign can be appropriate.)... [Pg.112]

Equations (169) and (171), together with Eqs. (170), fomi the basic equations that enable the calculation of the non-adiabatic coupling matrix. As is noticed, this set of equations creates a hierarchy of approximations starting with the assumption that the cross-products on the right-hand side of Eq. (171) have small values because at any point in configuration space at least one of the multipliers in the product is small [115]. [Pg.698]

The basic equations of ZINDO/1 are the same as those m IXDO, except I orL i y. In stead of usiri g th e electron egativity in INDO, ZlNDO/l uses th e ion i,ration potential for computing Llj,... [Pg.294]

Aris, R., 1989. Vectors, Tensors and the Basic Equations of Fluid Mechanics, Dover Publications, New York. [Pg.15]

Before moving deeper into understanding what quantum mechanics means, it is useful to learn how the wavefunctions E are found by applying the basic equation of quantum mechanics, the Schrodinger equation, to a few exactly soluble model problems. Knowing the solutions to these easy yet chemically very relevant models will then facilitate learning more of the details about the structure of quantum mechanics because these model cases can be used as concrete examples. ... [Pg.10]

The Roothaan equations are the basic equations for closed-shell RHF molecular orbitals, and the Pople-Nesbet equations are the basic equations for open-shell UHF molecular orbitals. The Pople-Nesbet equations are essentially just the generalization of the Roothaan equations to the case where the spatials /j and /jP, as shown previously, are not defined to be identical but are solved independently. [Pg.227]

In conclusion, it should further be noted that, as will be explained in Section 3.8, the quantity d 4 of the basic equation (3.51) is equal to the area of the core walls only if the capillary is of constant cross-section. If it tapers either outwards or inwards, a correction to d/i is required. [Pg.149]

Section 3.7, the gas adsorption method breaks down for practical reasons. Since the angle of contact of mercury with solids is 140° (see later), and therefore more than 90°, an excess pressure Ap is required to force liquid mercury into the pores of a soh d. The idea of using mercury intrusion to measure pore size appears to have been first suggested by Washburn who put forward the basic equation... [Pg.175]

Copolymers. Although many copolymers of ethylene can be made, only a few have been commercially produced. These commercially important copolymers are Hsted in Table 4, along with their respective reactivity coefficient (see Co polymers. The basic equation governing the composition of the copolymer is as follows, where and M2 are the monomer feed compositions, and r2 ate the reactivity ratios (6). [Pg.375]

Capillary Viscometers. Capillary flow measurement is a popular method for measuring viscosity (21,145,146) it is also the oldest. A Hquid drains or is forced through a fine-bore tube, and the viscosity is determined from the measured flow, appHed pressure, and tube dimensions. The basic equation is the Hagen-Poiseuike expression (eq. 17), where Tj is the viscosity, r the radius of the capillary, /S.p the pressure drop through the capillary, IV the volume of hquid that flows in time /, and U the length of the capillary. [Pg.180]

In the large-diameter vertical cylindrical tanks, because hoop stress is proportional to diameter, the thickness is set by the hydrostatic hoop stresses. Although the hydrostatic forces increase proportionally with the depth of Hquid in the tank, the thickness must be based on the hydrostatic pressure at the point of greatest depth in the tank. At the bottom, however, the expansion of the shell owing to internal hydrostatic pressure is limited so that the actual point of maximum stress is slightly above the bottom. Assuming this point to be about 1 ft (0.305 m) above the tank bottom provides tank shells of adequate strength. The basic equation modified for this anomaly is... [Pg.316]

The basic equational form of UNIFAC and many other QSARs is... [Pg.251]

Liquid Viscosity The viscosity of both pure hydrocarbon and pure nonhydrocarbon hquids are most accurately predicted by the method of van Velzen et al. The basic equation (2-112) depends on group contributions which are dependent on stnic tiire for the calculation of compound-specific constants B and To-... [Pg.409]

The method of Shebeko et al. " is the preferred flash point prediction method. The formula of the compound, the system pressure, and vapor pressure data for the compound must be available or estimable. Equation (2-174) is the basic equation. [Pg.418]

Perhaps the most useful of all Pitzer-type correlations is the one for the second virial coefficient. The basic equation (see Eq. [2-68]) is... [Pg.530]

Basic Equations AU of the processes described in this sec tion depend to some extent on the following background theory. Substances move through membranes by several meoianisms. For porous membranes, such as are used in microfiltration, viscous flow dominates the process. For electrodialytic membranes, the mass transfer is caused by an elec trical potential resulting in ionic conduction. For aU membranes, Ficldan diffusion is of some importance, and it is of dom-... [Pg.2024]

Basic Equations In Background and Definitions, the basic equation for gas permeation was derived with the major assumptions noted. Equation (22-62) may be restated as ... [Pg.2048]

One aspect of the basic equation describing biological treatment of waste that has not been referred to previously is that biomass appears on both sides of the equation. As was indicated above, the only reason that microorganisms function in waste-treatment systems is because it enables them to reproduce. Thus, the quantity of biomass in a waste-treatment system is higher after the treatment process than before it. [Pg.2216]


See other pages where Basic equations is mentioned: [Pg.345]    [Pg.1899]    [Pg.2101]    [Pg.227]    [Pg.1]    [Pg.2]    [Pg.2]    [Pg.4]    [Pg.6]    [Pg.8]    [Pg.10]    [Pg.12]    [Pg.14]    [Pg.16]    [Pg.61]    [Pg.73]    [Pg.101]    [Pg.40]    [Pg.78]    [Pg.1988]   


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Balancing Equations for Reactions Occurring in Basic Solution

Basic (MESH) Equations of Rigorous Distillation

Basic Decay Equations

Basic Definitions and Equations

Basic Equations Describing Chromatographic Separations

Basic Equations Used in Molecular Dynamics Calculations

Basic Equations and Boundary Conditions

Basic Equations for Adsorption

Basic Equations for Static and Dynamic Structure Factors

Basic Equations for Transfer of Heat, Mass, and Momentum

Basic Equations of Atmospheric Fluid Mechanics

Basic Equations of Electrokinetic Processes

Basic Equations of Fluid Flow

Basic Equations of Fluid Mechanics

Basic Equations of Growth

Basic Equations of Multicomponent Reacting Flows

Basic Equations of Statistical Thermodynamics - Partition function

Basic Equations of Structural Mechanics

Basic Equations of Surface Layer Atmospheric Fluid Mechanics

Basic Grand Ensemble Equations

Basic Kinetic Equations

Basic Michaelis-Menten Equation

Basic Principles and Equations

Basic X-ray diffraction equations

Basic design equations for a tubular reactor

Basic differential equation

Basic electromagnetic laws and Maxwells equations

Basic equation of fluid statics

Basic equations Of heat

Basic equations for gravity and magnetic fields

Basic equations for interfacial rheology

Basic equations for the analysis of chemical relaxations

Basic equations of elastic waves

Basic governing equations

Basic mathematical equations

Basic model and the rate equations

Basic model equation

Basic solution balancing oxidation-reduction equations

Basic solutions balancing redox equations

Basic stoichiometric equation

Basic system of equations

Bronsted equation in basicity

Chaos basic equations

Conductivity, electronic basic equation

Constitutive equation basic

Coupled cluster theory basic equation

Data analysis basic equations

Density basic equation

Derivation of Basic Equation

Differential Equations the Basic Reduction to First Order Systems

Diffusion Basic equations

Dispersed plug flow model basic differential equation

Dual basicity equation

Eight Basic Equations of Thermodynamics

Electromagnetic theory basic equations

Equation basic sedimentation

Equilibrium equation, basic sedimentation

Filtration operations—basic equations, compressible cakes

Filtration operations—basic equations, incompressible cakes

Final Form of the Basic Equation

Fluid flow basic equation

Fluid statics, basic equation

Formulation of Basic Equations

Half-reactions basic equations

Heat transfers Basic equations

Ionic strength basic equations

Langevin equation basic equations

Lattice dynamics basic equation

Mass spectrometry basic equations

Mass transfer analysis basic equation

Mathematics basic equations

Methods involving direct use of the basic equation

Oxidation-reduction equations basic solutions

Oxidation-reduction reactions basic equations

Photosynthesis basic, equation

Plug flow reactor basic performance equation

Rate equations, chemical basic

Rates, chemical reactions basic equations

Reaction rates basic rate equation

Reptation model basic equations

Schrodinger equation basic principles

Semiclassical Description Basic Equations

Specific basic equations formulation

Statics basic equation

System basic equations

THE BASIC EQUATION OF FLUID STATICS

The Basic Equations Describing Chromatographic Separations

The Basic Equations and Boundary Conditions

The Basic Equations of Vibrational Spectroscopy

The basic equations

The basic kinetic equations

The two basic equations

Theoretical treatment Basic equations

Theory and Derivation of Basic Equations

Thermal Design, Basic Equation

Thermal basic equations formulation

Thermodynamics basic equations

Timescales and basic equations of stellar structure

Transport equations, basic

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