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Enthalphy

An impulse-type turbine experiences its entire enthalphy drop in the nozzle, thus naving a very high velocity entering the rotor. The velocity entering the rotor is about twice the velocity of the wheel. The reaction type turbine divides the enthalphy drop in the nozzle and in the rotor. Thus, for example, a 50 percent reaction turbine has a velocity leaving the nozzle equal to the wheel speed and produces about V2 the work of a similar size impulse turbine at about 2-3 percentage points higher efficiency than the impulse turbine (0 percent reaction turbine). The effect on the efficiency and ratio of the wheel speed to inlet velocity is shown in Fig. 29-27 for an impiilse turbine and 50 percent reaction turbine. [Pg.2510]

Figure 2. (a) Excess enthalphies of n-butoxyethanol/water at 55.0 °C from four replicate titrations, starting at neat water (b) continuations of the titrations of (a). [Pg.297]

Figure 3. Excess enthalphies of aqueous solutions of n-butanol/water at 30.0 °C, compared to results from the literature squares, present results triangles, ref. 13 circles, ref.14 diamonds, interpolated from ref. 16. Figure 3. Excess enthalphies of aqueous solutions of n-butanol/water at 30.0 °C, compared to results from the literature squares, present results triangles, ref. 13 circles, ref.14 diamonds, interpolated from ref. 16.
The enthalphy change for this reaction at 25°C can be estimated from the algebraic summation of enthalphy changes for reactions that combine to give the same overall reaction (an application of Hess Law) ... [Pg.50]

Under such conditions, the free enthalphy curve at a given temperature shows two minima and one maximum as a function of x. [Pg.546]

An example is illustrated in Figure 8 for W/2.303 RT = 1.4. Two ranges of x values occur near the borders at x = 0 and x = 1, where the solid solutions are stable. The range of stability end at the x values which apply to the minima in the enthalphy curve, which are known as the limits of solid solubility Xgg. The two ranges of x values between the minima and the points of inflection in the enthalphy curve pertain to metastable solid solutions. The points of inflection occur at the so-called spinodal compositions X p (61). Between the two spinodal compositions any solid solution is unstable and will disproportionate into two solid solutions of the compositions Xgg. [Pg.549]

In that case, the enthalphy of mixing Hm should be of a form typical for subregular behavior such as ... [Pg.549]

The electron affinity (EA) for a molecule is a quantity which is analogous to the ionization energy for cations. Thus, the electron affinity is defined as the negative of the enthalphy change for the electron attachment reaction ... [Pg.256]

Ion cyclotron resonance (ICR) spectroscopy has been used to determine the reaction enthalphy (A//r) of hydride-transfer reaction of silanes with various hydrocarbons having known hydride affinities (Reaction 2.19). The hydride affinities of R3Si+, D//(X3Si+—H ) = Affbase, were obtained from Equation (2.20) and are summarized in Table 2.6 [30,31]-... [Pg.29]

The terms AHj, L, AH yUnd i used in Fig. 7.1 are all enthalphy changes defined as follows AHi is the heat of immersion of the solid into the liquid, L is the latent heat of condensation, AH yis the heat of adsorption when the solid is equilibrated with saturated vapor, and i is the heat liberated when solid in equilibrium with saturated vapor is immersed into liquid. Using Hess s law of heat summation... [Pg.47]

Thermal Properties. A typical dsc thermogram of an HPL/PVA blend (Fig. 4) shows a single Tg and Tm (10). Differences in the shape of the melting endotherms of PVA(96), (88), and (75) can be attributed to different degrees of crystallinity in the three polymers. Changes in crystalline structure of polymer blends usually result from polymer-polymer interactions in the amorphous phase. Such interactions result in a reduction of crystallinity, thereby reducing the enthalphy of the phase change (16,17). The observed reductions in melt endotherm area of HPL blends with PVA (> 0) may therefore indicate the existence of polymer-polymer interactions between the two types of macromolecules. [Pg.460]

Table 3.3. Standard enthalphies (heats) of formation of nickel aluminides and their effective heats of formation calculated for the effective concentration at the interface corresponding to the composition (3.5 at.% Ni, 96.5 at.% Al) of the eutectic with the lowest melting point in the Ni-Al binary system.261 For all the intermetallic compounds, the limiting element is nickel... Table 3.3. Standard enthalphies (heats) of formation of nickel aluminides and their effective heats of formation calculated for the effective concentration at the interface corresponding to the composition (3.5 at.% Ni, 96.5 at.% Al) of the eutectic with the lowest melting point in the Ni-Al binary system.261 For all the intermetallic compounds, the limiting element is nickel...
The outlet gas composition is normally computed by a trial and error procedure for each operating temperature the resulting composition is calculated, then the attained temperature is determined from an enthalphy balance and the temperature correspondence is checked. [Pg.395]

Although these epimerizations are general, they are only about as useful as the example given. In parentheses, we would like to compare them with the epimerization produced by molybdic acid (at 90°C in aqueous solution, pH 4.5) which does not involve a carbanion and is also general (Hayes et al. 1982). Glucose and mannose are at equilibrium, and the concentration ratio (2.5 1) is the one calculated from their free enthalphy difference. This is a typical reaction whose simplicity is misleading for there is simultaneous migration of the carbon atom at position 1 to position 2 (reaction 6.6). [Pg.221]

The decrease of enthalphy is the measure of reversible work that can be extracted from a flowing fluid upon expansion. [Pg.272]


See other pages where Enthalphy is mentioned: [Pg.519]    [Pg.2510]    [Pg.37]    [Pg.219]    [Pg.113]    [Pg.181]    [Pg.1649]    [Pg.187]    [Pg.117]    [Pg.129]    [Pg.209]    [Pg.209]    [Pg.62]    [Pg.45]    [Pg.240]    [Pg.126]    [Pg.169]    [Pg.39]    [Pg.2265]    [Pg.133]    [Pg.346]    [Pg.113]    [Pg.373]    [Pg.121]    [Pg.14]    [Pg.99]    [Pg.69]    [Pg.73]   
See also in sourсe #XX -- [ Pg.88 , Pg.275 ]

See also in sourсe #XX -- [ Pg.88 , Pg.275 ]




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Activation enthalphy

Enthalphy change

Excess enthalphies

Free enthalphies

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