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And the ideal gas temperature

The relationship between the thermodynamic temperature scale and the ideal gas temperature scale can be derived by calculating the thermodynamic quantities for a Camot cycle with an ideal gas as the working substance. Eor this purpose, we shall use 0 to represent the ideal gas temperamre. [Pg.122]

Thus, the thermodynamic and the ideal-gas temperature scales become the same if the values are selected to be identical at one finite temperature. [Pg.279]

Show, using the verbal statement of the second law, that if two reversible heat engines operate between the same temperatures, they have equal efficiencies. 3.52.a.What is the difference between the thermodynamic and the ideal gas temperature ... [Pg.106]

There are an infinite number of other integrating factors X with corresponding fiinctions ( ) the new quantities T and. S are chosen for convenience.. S is, of course, the entropy and T, a fiinction of 0 only, is the absolute temperature , which will turn out to be the ideal-gas temperature, 0jg. The constant C is just a scale factor detennining the size of the degree. [Pg.335]

Using generalized isothermal effects of pressure and the ideal gas state S and H values, the final temperature required to satisfy the condition AS = 0 is found, and the value of AH is determined for the path. [Pg.390]

Since kA depends on T, it remains inside the integral, and we must relate T to /A- Since the density (and hence q) changes during the reaction (because of changes in temperature and total moles), we relate q to fA and T with the aid of a stoichiometric table and the ideal-gas equation of state. [Pg.377]

The factor t + 273.2° will be recognized as the absolute temperature T of the gas. And since the ideal gas obeys Boyle s law, the product /Join is constant however pn and cn may vary between themselves. We may thus denote the coefficient /j( i o/273.2° by a single constant symbol, say R. and the ideal gas equation then takes the usual form... [Pg.820]

The Clapeyron equation is most often used to represent the relationship between the temperature dependence of a pure liquid s vapor pressure curve and its latent heat of vaporization. In this case, dPat/dT is the slope of the vapor pressure—temperature curve, A His the difference between the volume of the saturated vapor, H, and the saturated liquid, and AEFap is the latent heat of vaporization. Commonly, T) is small in comparison to V and the ideal gas law is assumed for the vapor phase. [Pg.233]

The ideal gas temperature scale is of especial interest, since it can be directly related to the thermodynamic temperature scale (see Sect. 3.7). The typical constant-volume gas thermometer conforms to the thermodynamic temperature scale within about 0.01 K or less at agreed fixed points such as the triple point of oxygen and the freezing points of metals such as silver and gold. The thermodynamic temperature scale requires only one fixed point and is independent of the nature of the substance used in the defining Carnot cycle. This is the triple point of water, which has an assigned value of 273.16 K with the use of a gas thermometer as the instrument of measurement. [Pg.6]

The Kelvin scale is thus defined in terms of an ideal reversible heat engine. At first such a scale does not appear to be practical, because all natural processes are irreversible. In a few cases, particularly at very low temperatures, a reversible process can be approximated and a temperature actually measured. However, in most cases this method of measuring temperatures is extremely inconvenient. Fortunately, as is proved in Section 3.7, the Kelvin scale is identical to the ideal gas temperature scale. In actual practice we use the International Practical Temperature Scale, which is defined to be as identical as possible to the ideal gas scale. Thus, the thermodynamic scale, the ideal gas scale, and the International Practical Temperature Scale are all consistent scales. Henceforth, we use the symbol T for each of these three scales and reserve the symbol 9 for any other thermodynamic scale. [Pg.34]

We prove the identity of the Kelvin scale and the ideal gas scale by using an ideal gas as the fluid in a reversible heat engine operating in a Carnot cycle between the temperatures T2 and 7. An ideal gas has been defined by Equations (2.36) and (2.37). Then the energy of an ideal gas depends upon the temperature alone, and is independent of the volume. [Pg.34]

This equation is identical to Equation (3.11). Therefore, the Kelvin thermodynamic scale and the ideal gas scale become identical when the temperature of the triple point of water is assigned the value of 273.16 K. [Pg.36]

These are the quantities to which we are giving our attention. Vibrational Raman scattering is being used for the temperature and density data, and, when taken simultaneously with velocity data from coupled LV instrumentation (.8), provides also the fluctuation mass flux through use of fast chemistry assumptions and the ideal gas law for atmospheric pressure flames. [Pg.212]

The state of a gas at the limiting condition where P - 0 deserves some discussion. As the pressure on a gas is decreased, the individual molecules become more and more widely separated. The volume of the molecules themselves becomes a smaller and smaller fraction of the total volume occupied by the gas. Furthermore, the forces of attraction between molecules become ever smaller because of the increasing distances between them. In the limit, as the pressure approaches zero, the molecules are separated by infinite distances. Their volumes become negligible compared with the total volume of the gas, and the inter-molecular forces approach zero. A gas which meets these conditions is said to be ideal, and the temperature scale established by Eq. (3.9) is known as the ideal-gas temperature scale. [Pg.38]

This equation relates temperature and volume for a mechanically reversible adiabatic process involving an ideal gas with constant heat capacities. The analogous relationships between temperature and pressure and between pressure and volume can be obtained from Eq. (3.22) and the ideal-gas equation. Since P, V,/ T, = P2V2j T2, we may eliminate V,/ V2 from Eq. (3.22), obtaining ... [Pg.41]

The tower is operating under a pressure of 70 psig, and a slot liquid seal of 2 in. is maintained. At the point of maximum volumetric vapor flow, the molecular weight of the vapor is 100, the rate of vapor flow is 1500 lb mol/h, the liquid density is 55 lb/ft3, and the temperature is 175°F. The pressure drop through the tower is negligible, and the ideal gas law is applicable to the rising vapors. Approximately what percent of the maximum allowable flow rate is being used in the tower ... [Pg.737]

The barometric distribution law gives the distribution of atmospheric gas molecules in terms of their molar mass M, height h, absolute temperature T, the acceleration due to gravity g, and the ideal gas constant R. The pressure p at height h is given in terms of that at zero height po as... [Pg.123]

We will review the basic quantities of thermodynamics energy, temperature, heat, work, and the ideal gas law. These quantities will be used to explain the principles of thermophysics and thermochemistry, which will be applied to the specific reactions of combustion and detonation. Using the thermochemical data of heats of detonation or explosion, we will see how to calculate adiabatic reaction temperatures. These data in turn will be used to analyze or predict pressures of explosions in closed vessels. We shall also see how, using thermochemical data, to predict detonation velocities and detonation pressures. [Pg.92]

A stream of propane at temperature T 423 K and pressure P(atm) flows at a rate of 100.0 kmol/h. Use the SRK equation of state to estimate the volumetric flow rate of the stream for P = 0.7 atm, 7 atm, and 70 atm. In each case, calculate the percentage differences between the predictions of the SRK equation and the ideal gas equation of state. [Pg.204]

Provided that the reaction temperature (and hence the rate of reaction) is high enough and the ideal gas equation of state is a reasonable approximation at the reactor outlet conditions (a questionable assumption), the ratio... [Pg.227]

Examples of employing the fluid dynamics or finite element method will be shown in the following sections. The methods can obviously be used also for variables other than the velocity, by a suitable selection of A in (3.50), such as, e.g., temperature, once the basic velocity field has been determined (as it enters in the equations for all other quantities). In the case of temperature T, the source term Ej in (3.50) includes external sources of heat and condensation, and the ideal gas law may be used to connect temperature and pressure. [Pg.150]

Property values in the standard state are denoted by the degree symbol. For example, Cp is the standard-state heat capacity. Since the standard state for gases is the ideal-gas state, Cp for gases is identical with Cp , and the data of Table C.l apply to the standard state for gases. All conditions for a standard state are fixed except temperature, which is always the temperature of the system. Standard-state properties are therefore functions of temperature only. The standard state chosenfor gases is a hypothetical one, for at 1 bar actual gases are not ideal. However, they seldom deviate much from ideality, and in most instances enthalpies for the real-gas state at 1 bar and the ideal-gas state are little different. [Pg.127]

On two different days the temperature and barometric pressure are the same. On day 1 the humidity is high, on day 2 the humidity is low. On which day is the air the most dense Justify your answer with arguments using Dalton s law and the ideal gas law. Why does the air feel heavier on day 1 than on day 21... [Pg.316]


See other pages where And the ideal gas temperature is mentioned: [Pg.36]    [Pg.36]    [Pg.336]    [Pg.167]    [Pg.63]    [Pg.14]    [Pg.33]    [Pg.41]    [Pg.114]    [Pg.125]    [Pg.7]    [Pg.67]    [Pg.21]    [Pg.174]    [Pg.18]    [Pg.97]    [Pg.62]    [Pg.500]    [Pg.196]    [Pg.3]    [Pg.398]    [Pg.140]    [Pg.150]    [Pg.53]   
See also in sourсe #XX -- [ Pg.40 , Pg.364 ]




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