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Theoretical functionality

The subject of entropy is introduced here to illustrate treatment of experimental data sets as distinct from continuous theoretical functions like Eq. (1-33). Thermodynamics and physical chemistry texts develop the equation... [Pg.24]

Techniques, such as spectroscopy (Chapter 10), potentiometry (Chapter 11), and voltammetry (Chapter 11), in which the signal is proportional to the relative amount of analyte in a sample are called concentration techniques. Since most concentration techniques rely on measuring an optical or electrical signal, they also are known as instrumental techniques. For a concentration technique, the relationship between the signal and the analyte is a theoretical function that depends on experimental conditions and the instrumentation used to measure the signal. For this reason the value of k in equation 3.2 must be determined experimentally. [Pg.38]

In its broad sense, an adsorption isotherm is an experimental or theoretical functional relationship between the adsorbed amount of a component and its amount in the bulk phase adjacent to the interface. Usually, the adsorption isotherm of a component i has the form... [Pg.123]

Here, N is the number of data points (time bins), yt the measured intensity in time bin i, of the measurement error (variance) for yh xt the time position of bin i, and / the theoretical function describing the decay. [Pg.137]

Experimentally, fN is determined as a function of temperature T, solvent composition x, and degree of polymerization N fN = F xp(T, x, N) here Fexp stands for the experimentally obtained functional form. On the other hand, statistical-mechanical formulations allow fN to be expressed in terms of s, a, and N fN = Flhcor(s, a, N), where Fth denotes a theoretical function. Then it should be possible from a comparison of F p and Flheor to determine s and a as functions of T and x. How can this be achieved Since the pioneering work of Zimm et al. (17) in 1959 various methods have been proposed. Typical approaches are outlined below for the experimental situation in which a thermally induced helix-coil transition is observed. For most of the proposed methods such transition curves must be available for a series of samples of different N. Preferably, these samples ought to be sharp in molecular weight distribution and cover as wide a range of N as possible. [Pg.79]

Fig. 15. Reduced sublattice magnetization as a function of the reduced temperature for K2CoF4. Full curve is the theoretical function of the 2-D Ising model... Fig. 15. Reduced sublattice magnetization as a function of the reduced temperature for K2CoF4. Full curve is the theoretical function of the 2-D Ising model...
This has been a theoretical treatment from the standpoint of reaction kinetics only, and I would like to reiterate the point made earlier—that a rate law for disappearance arrived at empirically could be, and perhaps would be, better used than a purely theoretical function. [Pg.138]

In a double logarithmic plot of P(q) vs. q, the asymptotic slope at high q of the upper envelope of the scattering curve depends on the ratio of the wall membrane thickness to the outer diameter, e.g -2 for an infinitely thin shell from Eq. (2) and -4 for a solid sphere from Eq. (3). By fitting an experimental scattering curve to the theoretical functional form of Eq. (I). two parameters. [Pg.251]

Solver (or Optimizer in Quattro Pro) can also be used to do least-squares fitting of data with a theoretical function that cannot be cast in the form required for the usual linear regression. As an illustration, Fig. 4 shows a radiative decay curve measured by a student for a raby crystal as part of Exp. 44. After laser excitation the digitized emission signal I decreases exponentially and can be analyzed for k (the radiative rate constant, whose reciprocal is the lifetime) according to the relation... [Pg.77]

Besides some particular cases such as ozonolysis2,3) or ring-opening polymerization of ketene-acetal type monomers4), the hydroxytelechelic polymers can be synthesized also by anionic polymerization. This process leads to polymers with smaller polydispersity and to a theoretical functionality of two free-radical polymerizations are easier to carry out, cheaper and, therefore, of industrial importance. Several reviews deal with the synthesis of functionally terminated polymers s>6 7, while this paper concerns only radical processes leading to hydroxytelechelic polymers. [Pg.169]

The x -test is useful for tests of goodness of fit , e.g. comparing expected and observed progeny frequencies in genetical experiments or comparing observed frequency distributions with some theoretical function. One limitation is that simple formulae for calculating f assume that no expected number is less than five. The G-test 21 test) is used in similar circumstances. [Pg.278]

This contradiction, however, is a merely verbal one, like lhatt)etween a tall wife and a short husband. The contrast is striking, but irrelevant -> since it provides no reason why the contradiction could not go on indefinitely. The notion of a social contradiction has the theoretical function of identifying causes of instability and change, not of locating symmetry violations. [Pg.48]

If the errors of the observations are well characterized, a statistical test can be applied to evaluate how well the data fit a given function. This can aid the investigator in deciding whether a theoretical or empirical function of the variables is satisfactory and whether a further critical evaluation of the theoretical function is justified. [Pg.342]

In cell B6 calculate y according to y = y0 e kt, and copy this down to B56. This will generate the theoretical function y0 e kt. [Pg.95]

The telechelic PTHF, with terminal hydroxyl groups, is obtained by the hydrolysis of structure 7.7 with sulfate ester units (reaction 7.8). The products of hydrolysis are sulfuric acid and hydroxy-telechelic PTHF with a practically theoretical functionality (f), of 2 OH groups/mol, without unsaturation. It is very important that the content of cyclic oligomers is extremely low, practically negligible. [Pg.240]

Chapter 12.5). Polyester polyols in reality, have the theoretical functionality, which is a great advantage for many polyurethane applications. For polyester diols the functionality is 2 OH groups/mol. This structural aspect results in the polyester diols giving PU elastomers with excellent physico-mechanical properties, superior to all polypropylene glycols obtained by anionic PO polymerisation. [Pg.269]

The resulting polybutadiene is a polymer with 1,4 cis, 1,4 trans and 1,2 microstructures. The resulting polybutadiene diol is perfectly linear having a high proportion of 1,2 microstructure (Figure 9.3). The functionality is very close to the theoretical functionality f = 2 OH groups/mol (92-93% bifunctional poly butadiene) [16-24]. [Pg.302]

The corrections mentioned, however, are rather approximate and thus one can enlarge the set of magnetic parameters for a temperature-independent term amol which compensates these uncertainties. Also, some cooperative ordering applicable at a low temperature can be included through the molecular field correction Z so that the theoretical function to be considered becomes... [Pg.337]


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See also in sourсe #XX -- [ Pg.269 ]




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