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Direction of change

At the point a (bp < 0) the directions of change are reversed, i.e.y all spontaneous changes increase the volume. [Pg.211]

The direction of change of pressure occurring in the distillation of a mixture of changing composition is fixed by a very general rule, deduced by Gibbs (1876), and used by Konowalow as a consequence of some experiments of Pliicker (1854), who found that the vapour pressure over a mixture of alcohol and water is all the less the larger the space which the vapour has to saturate. The rule may be stated as follows —... [Pg.384]

Because this problem asks for a qualitative answer, we do not need to do calculations. It is sufficient to apply Le Chatelier s principle to determine the direction of change and draw the new picture that shows the result of the change. [Pg.1160]

Fig.S.The nature and general pathway of the photocatalytic action of a semiconductor catalyst particle. Eg is the band gap, E shows the direction of change of the energy for electrons... Fig.S.The nature and general pathway of the photocatalytic action of a semiconductor catalyst particle. Eg is the band gap, E shows the direction of change of the energy for electrons...
It is important to realize that though the formulas for RME explicitly do not depend on reaction scale, x, since this variable cancels out in the computation, RME does in fact implicitly depend on reaction scale because reaction yields are scale dependent and RME in turn depends on reaction yield. Reaction yields are parameters whose magnitude cannot be predicted theoretically but must be verified experimentally. It does not always follow that a reported yield for a given reaction at a given scale will be the same at another scale. This requires experimental verification. Moreover, the direction of change as the scale is changed is also not predictable. AH of this means that when the same synthesis plan is run at a different scale, different reaction yields will be determined and hence different material efficiency performance values of RME, Em and mass of waste will be obtained. However, the... [Pg.109]

The reason that the Second Law has no quantitative relevance to nonequilibrium states is that it gives the direction of change, not the rate of change. So although it allows the calculation of the thermodynamic force that drives the system toward equilibrium, it does not provide a basis for calculating the all... [Pg.2]

Thus, as the pH increases, the dissolution rate of a weak base decreases. Referring to Table 2, we can see that, for the weak acid tolbutamide, the dissolution rate increases as pH is increased, as predicted by Eq. (3). Additionally, for the weak base tetracycline, as predicted by Eq. (4), the dissolution rate decreases as pH is increased. Thus far, the more rapid dissolution of the salt forms of these drugs and the direction of change of the dissolution rate with pH have been accounted for with Eqs. (1) to (4). However, there are six possible dissolution rate... [Pg.116]

C—C a bond to be cleft (Fig. 7.34). The LU of the C—C a part will conjugate with the HO of the n part of the ground-state polyene moiety in case of reaction, so that the orbital symmetry relations clearly determines the direction of bond fission. The direction of change is indicated by arrows. In this manner, in the thermal opening, the (4 )-chain will be... [Pg.72]

It is clear from the change in activity over this composition range that the surface composition of the Pd-Rh crystallites varied and, as expected, the direction of change indicates an increasing Rh surface content (Fig. 27). There is a maximum in activity at 52% Rh, but at slightly smaller Rh content the rate is distinctly less these anomalous results (open circles in Fig. 27) are explained by the following treatment of the data. The surface composition was equated with the composition corresponding to the observed lattice constant of phase I. In Fig. 28 the catalytic activity... [Pg.175]

In a process at constant T and V in a closed system doing only expansion work it follows from eq. (1.32) that the spontaneous direction of change is in the direction of decreasing A. At equilibrium the value of A is at a minimum. [Pg.14]

These arguments represent a simple example of phase equilibria. This branch of thermodynamics tells us about the direction of change, but says nothing about the rate at which such changes occur. [Pg.182]

In fact, it does not matter whether AH relates to the direction of change of solid - liquid or of liquid - solid, provided that AV relates to the same direction of change. [Pg.194]

If we write a similar expression to that in Equation (7.40) for the reaction between sodium metal and water in Equation (7.35), then we would have to write the term for the hydrogen couple first rather than second, because the direction of change within the couple is reversed. In fact, any couple that caused hydrogen gas to form protons would be written with the hydrogen couple first, and any couple that formed hydrogen gas from protons (the reverse reaction) would be written with the hydrogen term second. [Pg.323]

Another factor that affected the direction of change in family income was its place on the economic ladder. The closer a family was V to poverty the more likely they were to see their income rise. Whereas, 45% of families at the top of the economic ladder, those with income-to-poverty ratios of more than 4.0, experienced income decreases in 1994. While age, gender, and race play a significant role in determining one s place on the economic ladder, these factors are 00) not good predictors of a rise or fall in income. The only population for which one of these factors was significant was the elderly, whose incomes tended to be fairly stable. [Pg.247]

The major directions of changing porosity in DRP are schematically shown in Figure 9.22 [3,61], As a starting point, one can use the porosity of DRP of monospheres s0 = 0.36-0.42. Values of >s0 increase with particles anisotropy, roughness, and internal porosity, and also with the influence of wall effects at K> 0.1, and DIH > 0.05. Values of < (J are characteristic for polydis-perse particles when denser zones with ordered or unidirectional packings are formed, and also under forced densification and deformation of particles, correspondingly. [Pg.289]

Table 5.3. Alteration of Membrane Lipid Properties and the Resultant Approximate Directions of Changes of Fluorescence Parameters of a Typical Membrane Fluorophore Probe of the Fatty Acyl Chain Region0... Table 5.3. Alteration of Membrane Lipid Properties and the Resultant Approximate Directions of Changes of Fluorescence Parameters of a Typical Membrane Fluorophore Probe of the Fatty Acyl Chain Region0...
The second law of thermodynamics introduces a new function of state, the entropy, S, in order to quantify the spontaneity and direction of change for natural systems... [Pg.78]

Type of reaction Change to system Effect on Direction of change... [Pg.365]

As the actual work done approaches the reversible work, the pressure P of the gas and the external pressure P differ infinitesimally, and the direction of change can be... [Pg.84]


See other pages where Direction of change is mentioned: [Pg.344]    [Pg.17]    [Pg.756]    [Pg.73]    [Pg.1181]    [Pg.49]    [Pg.386]    [Pg.422]    [Pg.484]    [Pg.508]    [Pg.513]    [Pg.43]    [Pg.35]    [Pg.73]    [Pg.101]    [Pg.328]    [Pg.362]    [Pg.427]    [Pg.304]    [Pg.720]    [Pg.83]    [Pg.129]    [Pg.353]    [Pg.78]    [Pg.17]    [Pg.125]    [Pg.210]    [Pg.332]    [Pg.222]   
See also in sourсe #XX -- [ Pg.130 ]




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