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Vaporization, heat independent

If it is assumed that the molar heat of vaporization is independent of temperature, then the equation integrates to... [Pg.286]

The activation energy obtained from the dehydration (303-423 K) is almost constant and independent of the average pore diameter. The latent vaporization heat of water is fairly comparable (t2iHv = 40.9 kJ mol 1).33 In approximation of the applied formula, the desorption of adsorbed water can be depicted as a vaporization of liquid water out of the silica gel pores. [Pg.115]

The oxidation of CO on the surface of hopcalite is a reaction of zero order. Both a stoichiometric process resulting in the reduction of the oxide surface and a catalytic process with oxygen of the gas phase have been observed. The heat of activation for the catalytic process varies for different samples of hopcalite within the limits of 5 to 7 kcal. (64). Poisoning of the hopcalite surface by adsorption of water vapor is independent of the temperature. The catalytic reaction takes place on a definite and constant part of the surface and no additional active sections of surface are brought in to play if the temperature is increased. From a determination of the heats of wetting of water on hopcalite, it is apparent that the surface can be subdivided into two types with different heats of wetting (64). [Pg.189]

Now that we have some idea how to run ChemSep, let s use it to test the validity of the assumptions of the McCabe-Thiele method. The main assumption is "equiniolal overflow." We showed that if 1) you neglect sensible heat changes compared to latent heat and 2) you assume that the latent heat of vaporization is independent of composition, then the molar flowrates of liquid and vapor streams do not vary from stage to stage. [Pg.133]

As state functions, Cv and Cp depend on pressure and temperature. This dependence is illustrated for Cp in Figure 3-8. which shows the constant-pressure heat capacity of water as a function of pressure at selected temperatures. In general, the heat capacity of the liquid is higher than that of the vapor heat capacity is a strong function of pressure in the vapor phase but almost independent of pressure in the liquid. In both phases, Cp is fairly sensitive on temperature. Following an isotherm to zero pressure we... [Pg.105]

Theoretically the enthalpy of vaporization is independent of the heating rate. In practice it is not independent, but shows a variable increase at increasing heating rates. However, the maximum temperatures of the evaporation peaks do shift depending on the heating rates. This fact permits the ealculation of the aetivation energy of the evaporation process, which does not exhibit any temperature dependence. Theoretical considerations lead to the eonclusion that this aetivation energy is equal to the molar enthalpy of vaporization. [Pg.81]

The design of the calorimeter is shown in Figure 9.19. The calorimeter consists of a burner and an electrical compensation heater in a double-walled heat pipe filled with Freon with a boiling point of 25 °C. The Freon transports the heat, which is developed by the burner and the compensation heater, to a cooling unit that consists of water-cooled Peltier elements. A thermometer located in the vapor phase is used to control the power of the compensation heater so as to keep the temperature of the vapor constant independent of the heat of combustion of the gas. The flow of gas burned in the calorimeter is determined by means of mass... [Pg.277]

For a segment in a chain, the translation along the main chain is possible as a whole, but the independent translational motion of a segment is not allowed, as shown in Fig. 6. Therefore, two directions perpendicular to the chain axis are available for the free translation of a segment. For a segment, the vaporization heat is replaced by a product of cohesion heat Hq times the number of coordination, which is two less than that of the free unit, that is, z. [Pg.419]

Since the Schmidt number, Prandtl number, latent heat of vaporization, and humid heat are all essentially independent of pressure, the adiabatic-saturation-temperature and wet-bulb-temperature hues will be substantially equal at pressures different from atmospheric. [Pg.1161]

Multilayered materials owe their properties and behavior to the properties of and the interactions between the components (5). Each of the two or more components contributes its particular property to the total performance of the multilayered material. For example, in Pouch 1, Table II, the aluminum foil provides high oxygen and water vapor permeability resistance, poly (ethylene terephthalate) provides structural strength and stiffness, and the ethylene-butene copolymer provides a heat sealable layer. If the components of the multilayered materials interact then the whole would be something different than the sum of its parts. In other words, the properties of the components of the multilayered materials are not independent of one another but rather are interdependent. [Pg.97]

Heat transfer characteristics for saturated boiling were considered by Yen et al. (2003). From this study of convective boiling of HCFC123 andFC72 in micro-tubes with inner diameter 190, 300 and 510 pm one can see that in the saturated boiling regime, the heat transfer coefficient monotonically decreased with increasing vapor quality, but independent of mass flux. [Pg.301]

To describe the flow in a horizontal heated capillary we use the mass, momentum and energy balance equations. At moderate velocity, the effects due to compressibility of liquid and vapor, as well as energy dissipation in gaseous and liquid phases are negligible. Assuming that thermal conductivity and viscosity of the vapor and the liquid are independent of temperature and pressure, we arrive at the following system of equations ... [Pg.382]

Both of the above chemical studies point towards the increased importance of the burning process at 285°C in determining the initial rate of heat production. The role of water as yet remains undefined other than at the higher temperature of 285°C it appears to have the opposite effect on the bitumen sample compared to the process at 225°C i.e., it appears that water vapor encourages pathways by which the various components of bitumen react with oxygen. Preliminary calculations of the total heats evolved during the wet oxidation of bitumen sands indicate that they are independent of the partial pressure of oxygen in the system at... [Pg.442]

Authors note The measured independence of the sublimation rate from the layer thickness shows, that the sublimation rate under the conditions of the experiment depends only from the heat transfer to the product and not from the water vapor transportation through the dried product.)... [Pg.217]

If a more complex mathematical model is employed to represent the evaporation process, you must shift from analytic to numerical methods. The material and enthalpy balances become complicated functions of temperature (and pressure). Usually all of the system parameters are specified except for the heat transfer areas in each effect (n unknown variables) and the vapor temperatures in each effect excluding the last one (n — 1 unknown variables). The model introduces n independent equations that serve as constraints, many of which are nonlinear, plus nonlinear relations among the temperatures, concentrations, and physical properties such as the enthalpy and the heat transfer coefficient. [Pg.434]


See other pages where Vaporization, heat independent is mentioned: [Pg.55]    [Pg.1062]    [Pg.86]    [Pg.181]    [Pg.199]    [Pg.2109]    [Pg.193]    [Pg.1622]    [Pg.211]    [Pg.990]    [Pg.1261]    [Pg.373]    [Pg.255]    [Pg.512]    [Pg.47]    [Pg.1264]    [Pg.2304]    [Pg.105]    [Pg.212]    [Pg.34]    [Pg.347]    [Pg.142]    [Pg.433]    [Pg.434]    [Pg.435]    [Pg.120]    [Pg.127]    [Pg.997]    [Pg.61]    [Pg.110]    [Pg.289]    [Pg.490]    [Pg.671]    [Pg.38]    [Pg.96]   
See also in sourсe #XX -- [ Pg.213 ]

See also in sourсe #XX -- [ Pg.213 ]




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Vaporization, heat

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