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Temperature for gases

Figure 8-9. Equilibrium water dew points at different temperatures for gases. Figure 8-9. Equilibrium water dew points at different temperatures for gases.
Thermal conductivity does not remain constant with temperature. For gases, the thermal conductivity increases with (the square root of) temperature. The atoms in a higher tem-... [Pg.200]

Absolute Specific Gravity (Abs sp gr, sp gr, d j or S) can be defined as the ratio of true weight of a substance (wt corrected to air buoyancy) to true wt of water contained in the same volume at the same temperature. For gases, the term sp gr refers to dry air at the same pressure temp. In US industries, the term "specific gravity", without the prefix "absolure" may refer to wts not corrected to the effects of air buoyancy (apparent wts). The sp grs using the uncorrected wts are known in science as Apparent Specific Gravities and they do not differ more than 0.1% from the sbsolute values (See also Ref 2, p 411 Ref 13, p 876... [Pg.486]

Notice that the difference between the adiabatic wall temperature and the actual wall temperature is used in the definition so that the expression will yield a value of zero heat flow when the wall is at the adiabatic wall temperature. For gases with Prandtl numbers near unity the following relations for the recovery factor have been derived ... [Pg.254]

Values of v calculated in this maimer for gases of various specific gravity are shown in Figure 53. In these charts the value of v is plotted as a fimction of reservoir pressure and temperature for gases with gravities of 0.60, 0.70, 0.80, and 0.90. For other gas gravities... [Pg.104]

If additional significant figures are needed, 273.15 can be used in place of 273. The standard temperature for gases is 0°C, which is 273 K, a benchmark temperature used when comparing volumes of gases. No degree symbol is used with Kelvin temperatures. More information about the Kelvin temperature scale appears in the discussion of Charles law. [Pg.297]

The specific gravity of a liquid or a solid is the ratio of the density of the material to the density of water. Therefore, it is essentially independent of temperature. For gases, the comparison material is air. [Pg.450]

Ifitschfelder et al. [H9] gives a generalized relation for the variation of the thermal diffusion constant with temperature for gases whose molecules interact with the so-called Lennard-Jones potential function, the difference between a repulsion energy inversely... [Pg.911]

To find the adiabatic saturation temperature for gases other than air, a heat balance similar to Eq. (23.11) is used. It may be more convenient, however, to use molar heat capacities, as in the following example. [Pg.741]

The adsorption isotherm is the equilibrium relationship between the concentration in the fluid phase and the concentration in the adsorbent particles at a given temperature. For gases, the concentration is usually given in mole percent or as a partial pressure. For liquids, the concentration is often expressed in mass units, such as part per million. The concentration of adsorbate on the solid is given as mass adsorbed per unit mass of original adsorbent. [Pg.814]

Thus the solubility of a gas increases with increasing temperature for gases very much above their.critical temperature, and decreases with increasing temperature at temperatures near or only slightly above the critical temperature. This conclusion is in agreement with the experimental data of Fig. 11.1-3. [Pg.584]

The years 1859 to 1861, when the Ministry of Public Instruction sent him abroad to study, shaped Mendeleev s career as a scientist. He studied gas density with the chemist Henri Victor Regnault in Paris and spectroscopy with the physicist Gnstav Kirchhoff in Heidelberg. It was while working in Heidelberg that Mendeleev discovered the principle of critical temperature for gases. Once a gas is heated to a temperature above its critical point, no amount of pressure will turn it into a liqtiid. His work went unnoticed, and the discovery of critical temperatures is usually attributed to the Irish physicist and chemist Thomas Andrews. [Pg.775]

The specific heat represents the amount of energy required to raise a unit mass one unit in temperature. For gases, the specific heat differs depending on whether the gas is allowed to do work by expanding against an atmosphere (constant pressure definition, c, ) or is constrained within a volume (constant volume definition, c ). Examples of units of c, and are J/g K or Btu/lbm °F. If we wish to express this on a molar basis we shall use the upper case that is, or Q having units of J/mol K or Btu/lbmol °F. [Pg.78]

The equilibrium constant is a function only of temperature for gases, K = K T), and a function of temperature and pressure, K = K(T,p), for liquids when convention a is used. The equilibrium constant is a function of T, p and the solvent in liquids when convention b is used. The equilibrium constant can also be expressed in terms of the equilibrium activities by substituting Eq. (8-38) into Eq. (8-44) to yield... [Pg.106]

For both gases and vapors the diffusivity increases with increasing temperature. The solubility increases with temperature for gases but decreases for vapors. The change in the heat of solution is usually smaller than the change in the activation energy for diffusion. It follows from this that permeability increases with increasing temperature other than in exceptional circumstances. [Pg.750]

Effect of pressure on CPT for gases UnliKc liquids where a pressure increase often enhances the wax precipitation at constant temperature, for gases pressure has often the opposite effect pre.s.> ure increase may inhibit the precipitation at constant temperature. The solubility of nC- s in CO2 at 308 K. and the solubility of nC2o in Cj are provided in Tables 5.11 and 5.12 below. First derive the expression... [Pg.345]

The solubility of a substance is the amount of that substance required to form a saturated solution with a specific amount of solvent at a specified temperature. The solubility of sugar, for example, is 204 g per 100. g of water at 20.°C. The temperature must be specified because solubility varies with temperature. For gases, the pressure must also be specified. Solubilities must be determined experimentally and can vary widely, as shown in Figure 2.4. Solubility values are usually given as grams of solute per 100. g of solvent or per 100. mL of solvent at a given temperature. [Pg.388]

Think About It With the pressure held constant, we should expect the volume to increase with increased temperature. Room temperature is higher than the standard temperature for gases (0°C), so the molar volume at room temperature (25°C) should be higher than the molar volume at 0°C— and it is. [Pg.428]

Student Annotation In thermochemistry we often used 25°C as the "standard" temperature—although temperature is not actually part of the definition of the standard state [Mt Section 5.6]. The standard temperature for gases is defined specifically asO°C... [Pg.456]

See Problem 7.1. The Boyle-point temperature is defined as that temperature at which a = 0 for P = 0. From Figure A.4 estimate the Boyle-point temperature for gases that follow that chart. What is the practical significance of the Boyle point ... [Pg.104]

Table 5.11 Henry s Law Constants (atm cm /mol) as a Function of Temperature for Gases into Water... Table 5.11 Henry s Law Constants (atm cm /mol) as a Function of Temperature for Gases into Water...
Because gas properties depend on temperature and pressure, it is useful to have a set of standard conditions of temperature and pressure that can be used for comparing different gases. The standard temperature for gases is taken to be 0 °C = 273.15 K and standard pressure, 1 bar = 100 kPa = 10 Pa. Standard conditions of temperature and pressure are usually abbreviated as STP. It is important to emphasize that STP was defined differently in the past, and some... [Pg.203]


See other pages where Temperature for gases is mentioned: [Pg.744]    [Pg.27]    [Pg.371]    [Pg.487]    [Pg.31]    [Pg.487]    [Pg.84]    [Pg.744]    [Pg.302]    [Pg.428]    [Pg.114]   
See also in sourсe #XX -- [ Pg.64 ]




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