Coefficient proportionality

Boltzmann constant constant for layer growth reaction constant logarithmic rate constant linear rate constant parabolic rate constant reaction coefficient proportionality constant stress intensity factor fracture toughness diffusion path length length of sample... 

Temperature dependent Henry s law coefficient Proportionality constant... 

This expression shows diat if die detuning Acuj is negative (i.e. red detuned from resonance), dieii die cooling force will oppose die motion and be proportional to die atomic velocity. The one-diniensional motion of die atom, subject to an opposing force proportional to its velocity, is described by a damped haniionic oscillator. The Doppler damping or friction coefficient is die proportionality factor. 

For isotropic media we will assume tliat P is parallel to E witli tire coefficient of proportionality independent of direction ... 

The application of a small external electric field A to a semiconductor results in a net average velocity component of the carriers (electrons or holes) called the drift velocity, v. The coefficient of proportionality between E and is known as the carrier mobility p. At higher fields, where the drift velocity becomes comparable to the thennal... 

Apart from some numerical coefficients, the details of which we shall forgo, the required proportionality factor involves kT and the concentration of entanglement points. Multiplying Eq. (2.67) by these factors, we obtain... 

A solution which obeys Raoult s law over the full range of compositions is called an ideal solution (see Example 7.1). Equation (8.22) describes the relationship between activity and mole fraction for ideal solutions. In the case of nonideal solutions, the nonideality may be taken into account by introducing an activity coefficient as a factor of proportionality into Eq. (8.22). 

In Sec. 2.2 we saw that the coefficient of viscosity is defined as the factor of proportionality between the shearing force per unit area = F /A and the velocity gradient dv/dy within a liquid [Eq. (2.2)] ... 

In this expression, called Pick s first law, the proportionality constant D is the diffusion coefficient of the solute. Since J = (l/A)(dQ/dt) and c = Q/V, where Q signifies the quantity of solute in unspecified units, it follows that D has the units length time", or m sec in the SI system. The minus sign in Eq. (9.69)... 

This shows that Schlieren optics provide a means for directly monitoring concentration gradients. The value of the diffusion coefficient which is consistent with the variation of dn/dx with x and t can be determined from the normal distribution function. Methods that avoid the difficulty associated with locating the inflection point have been developed, and it can be shown that the area under a Schlieren peak divided by its maximum height equals (47rDt). Since there are no unknown proportionality factors in this expression, D can be determined from Schlieren spectra measured at known times. 

Friction and Adhesion. The coefficient of friction p. is the constant of proportionality between the normal force P between two materials in contact and the perpendicular force F required to move one of the materials relative to the other. Macroscopic friction occurs from the contact of asperities on opposing surfaces as they sHde past each other. On the atomic level friction occurs from the formation of bonds between adjacent atoms as they sHde past one another. Friction coefficients are usually measured using a sliding pin on a disk arrangement. Friction coefficients for ceramic fibers in a matrix have been measured using fiber pushout tests (53). For various material combinations (43) ... 

Diffusion is the molecular transport of mass without flow. The diffu-sivity (D) or diffusion coefficient is the proportionality constant between the diffusion and the concentration gradient causing diffusion. It is usually defined by Fick s first law for one-dimensional, binary component diffusion for molecular transport without turbulence shown by Eq. (2-149)... 

A proportionality between the theoretical spall strength and the bulk modulus is obtained when a two-parameter model is chosen to represent the intermolecular potential. Other two-parameter representations of the intermolecular potential, such as the Lennard-Jones 6-12 potential, will yield a similar proportionality although the numerical coefficients will differ slightly. 

It should be noted that low-loss spectra are basically connected to optical properties of materials. This is because for small scattering angles the energy-differential cross-section dfj/dF, in other words the intensity of the EEL spectrum measured, is directly proportional to Im -l/ (E,q) [2.171]. Here e = ei + iez is the complex dielectric function, E the energy loss, and q the momentum vector. Owing to the comparison to optics (jqj = 0) the above quoted proportionality is fulfilled if the spectrum has been recorded with a reasonably small collection aperture. When Im -l/ is gathered its real part can be determined, by the Kramers-Kronig transformation, and subsequently such optical quantities as refraction index, absorption coefficient, and reflectivity. 

Volumetric mass transfer coefficient, kLa The proportionality coefficient reflecting both molecular diffusion, turbulent mass transfer, and specific area for mass transfer. 

The proportionality constant, h, is influenced by the nature of the fluid and the nature of the agitation and is determined experimentally. If agila-tion does not exist, h is only influenced by the nature of the fluid and is called the film coefficient. 

Irreversible thermodynamics has also been used sometimes to explain reverse osmosis [14,15]. If it can be assumed that the thermodynamic forces responsible for reverse osmosis are sufficiently small, then a linear relationship will exist between the forces and the fluxes in the system, with the coefficients of proportionality then referred to as the phenomenological coefficients. These coefficients are generally notoriously difficult to obtain, although some progress has been made recently using approaches such as cell models [15]. 

The proportionality constant k is called the rate constant (or rate coefficient or specific rate). The rate constant is independent of the concentrations of A, B,. .., but may depend upon environmental factors such as the temperature and solvent, and of course its magnitude depends on the particular reaction being studied. 

Second, we take account of the frictional drag as the solute molecule moves through the solvent. The frictional force is taken to be proportional to the velocity of the particle, with a proportionality constant called the friction coefficient... 

In this equation, % is a proportionality factor known as the bead-solvent friction coefficient which purports to account in some kind of average way for the complex molecular interactions as the polymer segments (schematized by the bead) move about in the solvent. Following Stokes law of drag resistance, this friction coefficient is usually given as = 67trisa, with a equal to the bead radius. 

R is the shear stress in the fluid and divelocity gradient or the rate of shear. It may be noted that R corresponds to r used by many authors to denote shear stress similarly, shear rate may be denoted by either dw,/dy or y. The proportionality sign may be replaced by the introduction of the proportionality factor n, which is the coefficient of viscosity, to give ... 

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