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Temperature, absolute Kelvin

Numerous mathematical formulas relating the temperature and pressure of the gas phase in equilibrium with the condensed phase have been proposed. The Antoine equation (Eq. 1) gives good correlation with experimental values. Equation 2 is simpler and is often suitable over restricted temperature ranges. In these equations, and the derived differential coefficients for use in the Hag-genmacher and Clausius-Clapeyron equations, the p term is the vapor pressure of the compound in pounds per square inch (psi), the t term is the temperature in degrees Celsius, and the T term is the absolute temperature in kelvins (r°C -I- 273.15). [Pg.389]

Fig. 2. (a) Energy, E, versus wave vector, k, for free particle-like conduction band and valence band electrons (b) the corresponding density of available electron states, DOS, where Ep is Fermi energy (c) the Fermi-Dirac distribution, ie, the probabiUty P(E) that a state is occupied, where Kis the Boltzmann constant and Tis absolute temperature ia Kelvin. The tails of this distribution are exponential. The product of P(E) and DOS yields the energy distribution... [Pg.344]

Vitreous sihca does not react significantly with water under ambient conditions. The solution process involves the formation of monosilicic acid, Si(OH)4. Solubihty is fairly constant at low pH but increases rapidly when the pH exceeds 9 (84—86). Above a pH of 10.7 sihca dissolves mainly as soluble sihcates. Solubihty also increases with higher temperatures and pressures. At 200—400°C and 1—30 MPa (<10 300 atm), for example, the solubihty, S, of Si02 in g/kg H2O can be expressed as foUows, where d ls the density of the vapor phase and T is the absolute temperature in Kelvin. [Pg.500]

Vitreous siUca aimealed at 1100°C has been designated NIST Standard Reference Material 739 (LI and L2). Its expansion coefficient, a, may be calculated for 300—700 K from the following expression (144), where Tis the absolute temperature in Kelvin. [Pg.505]

The boiling points and freezing points in degrees Centigrade of certain liquids are listed below. Express these temperatures on the absolute temperature (degree Kelvin) scale. [Pg.63]

Absolute temperature, 57 Kelvin scale, 58 Absolute zero, 58... [Pg.455]

The Kelvin scale of absolute temperatures is described in Appendix IB the temperature in kelvins (K) is obtained by adding 273.15 to the temperature in degrees Celsius (°C). [Pg.268]

A note on good practice Note that the volume (or the pressure) doubles when the temperature is doubled on the absolute (Kelvin) scale, not when it is doubled on the Celsius scale. An increase from 20°C to 40°C corresponds to an increase from 293 K to 313 K, an increase of only 7%. [Pg.268]

The graphical plot of the temperature versus volume of a gas produces a straight line. If several different gases are studied and the temperature-volume data is plotted, the extrapolations of these graphs all intersect at the same temperature, -273°C. The Kelvin equivalent of this temperature is expressed as 0 K, or absolute zero. The mathematical expression to change Celsius temperature to Kelvin is K = C° + 273°. [Pg.105]

In the simplest ideal gas law problems, values for three of the four variables are given, and you are asked to calculate the value of the fourth. As usual with the gas laws, the temperature must be given as an absolute temperature, in kelvins. The units of P and V are most conveniently given in atmospheres and liters because the units of R with the value given above are in terms of these units. If other units are given for pressure or volume, convert them to atmospheres and liters, respectively. [Pg.190]

The values in this table are calculated from the equation K = e AE/RT where K is the equilibrium constant between isomers e 2.718 (the base of natural logarithms) AE = energy difference between isomers T= absolute temperature (in kelvins) and R = 1.986 cd mo /K (the gas constant). [Pg.161]

Strategy. For convenience, we will call the higher temperature T> and the lower temperature T. (1) The van t Hoff isochore, Equation (4.78), is written in terms of a ratio, so we do not need the absolute values. In other words, in this example, we can employ the solubilities s without further manipulation. We can dispense with the units of. v for the same reason. (2) We convert the two temperatures to kelvin, for the van t Hoff isochore requires thermodynamic temperatures, so T2 = 343.9 K and 7) = 312.0 K. (3) We insert values into the van t Hoff isochore (Equation (4.78)) ... [Pg.172]

At very low pressure all gases obey the ideal gas law, PV = nRT, where P is the pressure, V is the volume and, T is the temperature. The gas constant, R, is a universal constant, and T is the absolute temperature in kelvin. A mixture of gases at sufficiently low pressure also behaves ideally... [Pg.84]

This relationship for Newtonian viscosity is valid normally for temperatures higher than 50 °C or more above the Tg. The utility of the Arrhenius correlation can be limited to a relatively small temperature range for accurate predictions. The viscosity is usually described in this exponential function form in terms of an activation energy, Af, absolute temperature T in Kelvin, the reference temperature in Kelvin, the viscosity at the reference T, and the gas law constant Rg. As the temperature approaches Tg for PS (Tg = 100°C), which could be as high as 150°C, the viscosity becomes more temperature sensitive and is often described by the WLF equation [10] ... [Pg.102]

Lord Kelvin (1824-1907). The Kelvin temperature scale has an absolute zero. True comparisons can be made using the Kelvin scale. A substance at a temperature of 400 Kelvins contains particles with twice as much kinetic energy as a substance at 200 Kelvins. Absolute zero is the temperature where the random motion of particles in a substance stops. It is the absence of temperature. Absolute zero is equivalent to —273.16°C. How this value is determined is discussed shortly after we discuss our next gas law. The relationship between Kelvin and Celsius temperature is... [Pg.105]

When applying Charles Law it is important to remember that the absolute temperature must be used. Let s use the syringe example to determine how much the volume would increase if the temperature was raised from 20°C to 100°C. Let s assume the original volume at 20°C is 25 mL. First we ll convert the temperatures to Kelvins, and then apply Charles Law. The calculations are... [Pg.105]

According to Kelvin s definition, absolute Kelvin temperature TK can be consistently assigned in terms of the efficiency of the reversible engine operating between the two reservoir temperatures as... [Pg.130]


See other pages where Temperature, absolute Kelvin is mentioned: [Pg.277]    [Pg.676]    [Pg.277]    [Pg.676]    [Pg.122]    [Pg.171]    [Pg.345]    [Pg.404]    [Pg.481]    [Pg.122]    [Pg.458]    [Pg.13]    [Pg.388]    [Pg.75]    [Pg.44]    [Pg.97]    [Pg.83]    [Pg.50]    [Pg.103]    [Pg.263]    [Pg.566]    [Pg.270]    [Pg.345]    [Pg.197]    [Pg.628]    [Pg.404]    [Pg.27]    [Pg.66]    [Pg.584]    [Pg.171]    [Pg.129]    [Pg.3]   


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