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Change Function

Insofar as complex adaptive systems can be regarded as being essentially open-ended problem-solvers, their lifeblood consists mostly of novelty. The ability of a complex adaptive system to survive and evolve in a constantly changing environment is determiimd by its ability to continually find — either by chance, or experience, or more typically both insightful new strategies to increase its overall fitness (which is, of course, a constantly changing function in time). [Pg.566]

For hydrophobic, (virtually) nonionizable substances [i.e., those that show no ionic species of significance in the pH range 1 to 10 (e.g., diazepam)], solubility can usually be improved by addition of nonpolar solvents. Aside from solubility, stability is also affected by solvents in either a favorable or a nonfavorable direction [6], Theoretical equations for solubility in water [7] and in binary solvents [8] have been reported in literature, but in general the approach in preformulation is pseudoempirical. Most often the solubility changes as the concentration of nonpolar solvent C2, increases. For binary systems it may simply be a monotonely changing function [9], as shown in Fig. 2. The solubility is usually tied to the dielectric constant, and in a case such as that shown by the squares, the solubility is often log-linear when plotted as a function of inverse dielectric constant, E, that is,... [Pg.176]

A scaling argument does not describe the full functional form of the dependence of the chain dimensions on concentration. We would expect the dimensions of the polymer to be a smoothly changing function between c and the concentration J where the coils reach their limiting radius equivalent to the 6 dimensions. However, to a first approximation we can suppose that Equation (5.73) applies up to the concentration ct ... [Pg.183]

In the divergent method (Fig. 4), the molecule is assembled from the core to the periphery, while in the convergent method, the molecule is synthesized from the periphery to the core. In either method, the synthesis requires a stepwise process, attaching each layer to the previous one, purifying and then changing functional groups for the next stage of reaction. [Pg.157]

Physicist P. A. M. Dirac suggested an inspired notation for the Hilbert space of quantum mechanics [essentially, the Euclidean space of (9.20a, b) for / — oo, which introduces some subtleties not required for the finite-dimensional thermodynamic geometry]. Dirac s notation applies equally well to matrix equations [such as (9.7)-(9.19)] and to differential equations [such as Schrodinger s equation] that relate operators (mathematical objects that change functions or vectors of the space) and wavefunctions in quantum theory. Dirac s notation shows explicitly that the disparate-looking matrix mechanical vs. wave mechanical representations of quantum theory are actually equivalent, by exhibiting them in unified symbols that are free of the extraneous details of a particular mathematical representation. Dirac s notation can also help us to recognize such commonality in alternative mathematical representations of equilibrium thermodynamics. [Pg.324]

On this organic change, functional neurogenic vasoconstriction is superimposed. [Pg.5]

The state change function (same as the gamma output function) must be non-linear and key dependent. [Pg.309]

External stimulus Responsive membrane Recognition - Conformational change Functions... [Pg.156]

Adverse effect A biochemical change, functional impairment, or pathological lesion that either singly or in combination deleteriously affects the performance of the whole organism, or reduces an organism s ability to respond to an additional environmental challenge. [Pg.377]

EDIT allows the user to edit an individual gel independently of any others it may be related to. The commands are as for SEQEDT or EDIT NEW GEL in ENTER. The effect of this editing on the length of this gel or its relationship to others must be accounted for (if necessary) by use of the line change function. Maximum number of edit string characters is 200. [Pg.359]

While the above expression is widely used, it is also understood that this does not accurately reflect experimental data. The problem mainly arises due to the relatively discontinuous nature of the stability ratio demonstrated experimentally, a feature the above expression is not capable of predicting accurately (with such a sharply changing function, small discrepancies in terms can result in large differences in the value of the function). [Pg.517]

Eq. (3.2-16) shows that the frequency dependence of 6 is manifested through the dependence of the refractive index n on the radiation frequency. Since the spectral range in which optical materials are used is far enough from their absorption bands the dependence of n and hence of 6 on the frequency is a slightly and smoothly changing function in this spectral interval. Therefore, totally reflecting retarders are almost achromatic optical devices. [Pg.97]

As their name suggests, G protein-coupled receptors link ligand binding to intracellular changes functionally via their engagement of three distinct proteins (Ga, Gfi, Gy) known collectively as the G-protein heterotrimer (Fig. 1). The Ga subunit of the... [Pg.664]

Kidney slices Easy technique. Good control of experimental conditions without concern for secondary effects due to hemodynamic changes. Functional status of tubular lumen not clear. Tissue not homogenous and contains nontubular elements. Diffusion barrier for substrates to nephrons beneath the cut surface. [Pg.45]


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See also in sourсe #XX -- [ Pg.56 , Pg.85 ]




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AGha functional state change

Adsorption work function changes

Analytical Functions Wrapped Around Spheres Shape Change

Ascaris induced lung function changes

Catalyst work function changes

Change dielectric function during

Change of Gibbs Function

Change of Metric for Modified Wave Functions

Change of Work Function with Particle Size

Change of work function

Changes That Accompany Hemoglobin Function

Changes in State Functions

Conformational changes partition function

Contribution to Functional Change

Density functional perturbation theory energy change

Electron transfer rate constants, function free-energy change

Enthalpy change as a function of temperature

Estimation of Change in Enthalpy, Entropy, and Gibbs Function for Ideal Gases

Functional Changes in Dosage Forms with Time

Functional Properties of Phase Change Materials from Atomistic Simulations

Functional Roles in Supply Chain Change

Functional changes

Functional changes

Functional group changing

Functional group changing position

Functional group retrosynthetic changes

Functions approving document changes

Gibbs function changes

Harmonic change, spectral function

Isothermal change, free energy work function

Organic function, changes

Other Changes in Functional Form

Phase changes function

Planck function change

Renal function, change

Safety Culture Change Management Functions

Skeletal muscle changes function

Skin barrier function changes

Spontaneity Gibbs function change

Standard molar Gibbs function changes

Standard molar Gibbs function changes reactions

State function change

Structural Changes as a Function of Oxygen Stoichiometry

Supply chain change functional roles

Synthesis changing functional group

The Measurement of Work-Function Changes

Thermodynamic Changes, Properties and Types of Function

Work Function and Inner Potential Change

Work function changes

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