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Triple temperature

It is not known experimentally whether there is a similar critical point for solid-liquid phase transitions the experimentally available temperatures and pressures are insufficient to resolve this issue. The triple point (which really should be called a triple line) is a triple temperature (Tf) and a triple pressure (Pt) at which the three phases gas, liquid, and solid coexist, but with different volumes this triple line for several compounds is used to define reliable and reproducible standard temperatures for the International Temperature Scale. [Pg.260]

Due to the relation T = C pV, where C is a unknown calibration constant, this calibration constant can be measured by bringing the ideal gas in contact with a body at triple temperature of water. Then, by measurement of pressure and volume of the ideal gas which is in contact with a body of unknown temperature, this temperature can be measured. Again, this prescription of measurement of the absolute temperature is highly impracticable and suffers from the fact that an ideal gas exists, as the name indicates only ideally. [Pg.65]

According to calculation method above Cyy, K and R before and after storage can be calculated under the triple temperature levels. [Pg.1831]

TABLE 1 Critical and Triple Temperature for Rare Gases on Graphite... [Pg.436]

It is instructive, however, to set our finding also in context of the phase diagram. In Fig. 19 we plot binodals and spinodals as a function of composition x and temperature T at constant pa /ksT = 0.16. For the composition x = 0.68 the spinodal of the polymer-rich liquid is located at A Fspin/e = 0.675239, i.e., just 2% below the triple temperature. In the SCF calculations the nucleation barrier vanishes at Fspin,... [Pg.54]

The reason for this s-shaped form of the spinodal is an unstable liquid— liquid critical point. Below the triple temperature, there exists a polymer-rich liquid and a solvent-rich liquid. Both binodal and spinodal of the polymer-rich phase become richer in solvent upon increasing temperature. This tendency of the polymer-rich spinodal persists also above the triple temperature, the spinodal runs towards the (unstable) critical point of the liquid—liquid phase coexistence, which would terminate the liquid— liquid phase coexistence if it was not pre-emptied by liquid-vapor coexistence. The unstable critical points are marked by a square in Figs. 19 and 20 (a-c). The influence of the unstable liquid—liquid critical point is also detectable in the combination c of densities which becomes unstable at the spinodal. Initially, spinodal decomposition leads to a liquid-liquid phase separation. This effect also matches the observation slightly above the triple temperature that the critical bubble is not filled with solvent-vapor - the thermodynamically stable phase - but rather with liquid solvent. Only at temperatures farther above the triple temperature, the spinodal adopts the normal behavior and approaches the liquid-vapor critical point. In this region the unstable mode also changes from liquid-liquid to liquid-vapor. [Pg.55]

Transition matrix, Monte Carlo 17 Tricritical point/behavior 10, 12, 21 Tricritical universality class 93 Triple lines 5, 36, 38, 42, 43, 49, 50, 53, 56, 81, 89, 91, 94 Triple points 37, 39, 40, 54 Triple pressure 39, 40, 51 Triple temperature 53, 55 Two-chaiii equation 244... [Pg.273]

Equations (2) and (3) are physically meaningful only in the temperature range bounded by the triple-point temperature and the critical temperature. Nevertheless, it is often useful to extrapolate these equations either to lower or, more often, to higher temperatures. In this monograph we have extrapolated the function F [Equation (3)] to a reduced temperature of nearly 2. We do not recommend further extrapolation. For highly supercritical components it is better to use the unsymmetric normalization for activity coefficients as indicated in Chapter 2 and as discussed further in a later section of this chapter. [Pg.40]

Thermal conductivity is expressed in W/(m K) and measures the ease in which heat is transmitted through a thin layer of material. Conductivity of liquids, written as A, decreases in an essentially linear manner between the triple point and the boiling point temperatures. Beyond a reduced temperature of 0.8, the relationship is not at all linear. For estimation of conductivity we will distinguish two cases < )... [Pg.132]

At a given temperature and pressure, a pure compound can exist in one, two or three states. The compound exists at three different states at the triple point and at two different states along the curves of vaporization, freezing and sublimation. Refer to Figure 4.6. [Pg.148]

Triple point temperature K Heat of fusion kJ/lc Heat of vaporization kJ/kg Liquid conductivity atr, W / (m-K) Liquid conductivity AtT W/(m-I0 Temperature Ti K Temperature h K... [Pg.417]

Triple point temperature Heat of fusion Heat of vaporization Liquid conductivity at r, Liquid conductivity at Temperature Tx Temperature Tz... [Pg.421]

Triple point Heat of Heat of Liquid liquid Temperature Temperature... [Pg.437]

To understand the conditions which control sublimation, it is necessary to study the solid - liquid - vapour equilibria. In Fig. 1,19, 1 (compare Fig. 1,10, 1) the curve T IF is the vapour pressure curve of the liquid (i.e., it represents the conditions of equilibrium, temperature and pressure, for a system of liquid and vapour), and TS is the vapour pressure curve of the solid (i.e., the conditions under which the vapour and solid are in equili-hrium). The two curves intersect at T at this point, known as the triple point, solid, liquid and vapour coexist. The curve TV represents the... [Pg.37]

The normal melting point of a substance is the temperature at which solid and hquid are in equilibrium at atmospheric pressure. At the triple point, the pressure is the equilibrium vapour pressure of the system (solid liquid - vapour) and the temperature differs from the melting point. The difference is, however, quite small—usually only a fraction of a degree—since the line TV departs only slightly from the vertical within reasonable ranges of pressure. [Pg.38]

It is clear that if the vapour at a pressure below the triple point is reduced sufficiently in temperature, it will condense directly to the solid form, or, sublimation will ensue. In order that a solid may pass directly... [Pg.38]

For most practical purposes the temperature and pressure at the triple point may be regarded as not differing appreciably from the melting point and the vapour pressure at the melting point respectively. [Pg.38]

Temperature kelvin K Defined as the fraction 1/273.16 of the thermodynamic temperature of the triple point of water. [Pg.77]


See other pages where Triple temperature is mentioned: [Pg.101]    [Pg.390]    [Pg.53]    [Pg.49]    [Pg.251]    [Pg.335]    [Pg.809]    [Pg.410]    [Pg.436]    [Pg.49]    [Pg.53]    [Pg.54]    [Pg.101]    [Pg.390]    [Pg.53]    [Pg.49]    [Pg.251]    [Pg.335]    [Pg.809]    [Pg.410]    [Pg.436]    [Pg.49]    [Pg.53]    [Pg.54]    [Pg.407]    [Pg.172]    [Pg.172]    [Pg.172]    [Pg.497]    [Pg.98]    [Pg.610]    [Pg.210]    [Pg.38]    [Pg.39]    [Pg.39]    [Pg.81]    [Pg.60]    [Pg.477]   
See also in sourсe #XX -- [ Pg.41 , Pg.44 ]




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