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Mass transfer water

Prior to a discussion on the impact of processing air dew point and temperature on the drying rate behavior of a product, it is necessary to consider heat and mass transfer. Water will move from the granule to air in an attempt to reach an equilibrium, or saturated condition, determined by thermodynamics, which can be read from a phase diagram or psychrometric chart. The rate at which water will move from liquid in the granule to vapor in the air increases the further away the system is from equilibrium. When the water evaporates, it requires an amount of energy, the heat of vaporization, in order to change from liquid to vapor. Because of this, we must also consider transfer of heat as well as movement of material. These concepts can be described by equations shown in Table 5. [Pg.227]

The absorption of ozone from the gas occurred simultaneously with the reaction of the PAH inside the oil droplets. In order to prove that the mass transfer rates of ozone were not limiting in this case, the mass transfer gas/water was optimized and the influence of the mass transfer water/oil was studied by ozonating various oil/water-emulsions with defined oil droplet size distributions. No influence of the mean droplet diameter (1.2 15 pm) on the reaction rate of PAH was observed, consequently the chemical reaction was not controlled by mass transfer at the water/oil interface or diffusion inside the oil droplets. Therefore, a microkinetic description was possible by a first order reaction with regard to the PAH concentration (Kornmuller et al., 1997 a). The effects of pH variation and addition of scavengers indicated a selective direct reaction mechanism of PAH inside the oil droplets... [Pg.157]

Gagnon, G.A. and Huck, P.M., Removal of easily biodegradable organic compounds by drinking water biofilms analysis of kinetics and mass transfer. Water Res., 35(10), 2554, 2001. [Pg.407]

The value of the saturation concentration,, is the spatial average of the value determined from a clean water performance test and is not corrected for gas-side oxygen depletion therefore K ji is an apparent value because it is determined on the basis of an uncorrected. A tme volumetric mass transfer coefficient can be evaluated by correcting for the gas-side oxygen depletion. However, for design purposes, can be estimated from the surface saturation concentration and effective saturation depth by... [Pg.342]

Humidification. For wiater operation, or for special process requirements, humidification maybe required (see Simultaneous HEAT and mass transfer). Humidification can be effected by an air washer which employs direct water sprays (see Evaporation). Regulation is maintained by cycling the water sprays or by temperature control of the air or water. Where a large humidification capacity is required, an ejector which direcdy mixes air and water in a no22le may be employed. Steam may be used to power the no22le. Live low pressure steam can also be released directly into the air stream. Capillary-type humidifiers employ wetted porous media to provide extended air and water contact. Pan-type humidifiers are employed where the required capacity is small. A water filled pan is located on one side of the air duct. The water is heated electrically or by steam. The use of steam, however, necessitates additional boiler feed water treatment and may add odors to the air stream. Direct use of steam for humidification also requires careful attention to indoor air quahty. [Pg.362]

Chemical Equilibria. In many cases, mass transfer between two Hquid phases is accompanied by a chemical change. The transferring species can dissociate or polymerize depending on the nature of the solvent, or a reaction may occur between the transferring species and an extractant present in one phase. An example of the former case is the distribution of benzoic acid [65-85-0] between water and benzene. In the aqueous phase, the acid is partially dissociated ... [Pg.62]

The physical mass-transfer rate of o2one into water is affected by the gaseous o2one concentration, temperature, pressure, gas dispersion, turbulence, mixing, and composition of the solution, ie, pH, ionic strength, and the presence of reactive substances. Mass transfer of gaseous o2one into... [Pg.500]

The standard potential for the anodic reaction is 1.19 V, close to that of 1.228 V for water oxidation. In order to minimize the oxygen production from water oxidation, the cell is operated at a high potential that requires either platinum-coated or lead dioxide anodes. Various mechanisms have been proposed for the formation of perchlorates at the anode, including the discharge of chlorate ion to chlorate radical (87—89), the formation of active oxygen and subsequent formation of perchlorate (90), and the mass-transfer-controUed reaction of chlorate with adsorbed oxygen at the anode (91—93). Sodium dichromate is added to the electrolyte ia platinum anode cells to inhibit the reduction of perchlorates at the cathode. Sodium fluoride is used in the lead dioxide anode cells to improve current efficiency. [Pg.67]

For the air—water system, the humidity is easily measured by using a wet-bulb thermometer. Air passing the wet wick surrounding the thermometer bulb causes evaporation of moisture from the wick. The balance between heat transfer to the wick and energy requited by the latent heat of the mass transfer from the wick gives, at steady state,... [Pg.97]

The use of molal humidity as the mass-transfer driving force is conventional and convenient because of the development of humidity data for, especially, the air—water system. The mass-transfer coefficient must be expressed in consistent units. [Pg.97]

A closer look at the Lewis relation requires an examination of the heat- and mass-transfer mechanisms active in the entire path from the hquid—vapor interface into the bulk of the vapor phase. Such an examination yields the conclusion that, in order for the Lewis relation to hold, eddy diffusivities for heat- and mass-transfer must be equal, as must the thermal and mass diffusivities themselves. This equahty may be expected for simple monatomic and diatomic gases and vapors. Air having small concentrations of water vapor fits these criteria closely. [Pg.98]

The thermal design of cooling towers follows the same general procedures already presented. Integration of equation 35 is usually done numerically using the appropriate software, mass-transfer coefficients, saturation enthalpies, etc. In mechanical-draft towers the air and water dows are both suppHed by machines, and hence dow rates are fixed. Under these conditions the design procedure is straightforward. [Pg.104]

Work in the area of simultaneous heat and mass transfer has centered on the solution of equations such as 1—18 for cases where the stmcture and properties of a soHd phase must also be considered, as in drying (qv) or adsorption (qv), or where a chemical reaction takes place. Drying simulation (45—47) and drying of foods (48,49) have been particularly active subjects. In the adsorption area the separation of multicomponent fluid mixtures is influenced by comparative rates of diffusion and by interface temperatures (50,51). In the area of reactor studies there has been much interest in monolithic and honeycomb catalytic reactions (52,53) (see Exhaust control, industrial). Eor these kinds of appHcations psychrometric charts for systems other than air—water would be useful. The constmction of such has been considered (54). [Pg.106]

Ozone is only slightly soluble in water. Thus, factors that affect the mass transfer between the gas and Hquid phases are important and include temperature, pressure, contact time, contact surface area (bubble size), and pH. [Pg.163]

Under equiUbrium or near-equiUbrium conditions, the distribution of volatile species between gas and water phases can be described in terms of Henry s law. The rate of transfer of a compound across the water-gas phase boundary can be characterized by a mass-transfer coefficient and the activity gradient at the air—water interface. In addition, these substance-specific coefficients depend on the turbulence, interfacial area, and other conditions of the aquatic systems. They may be related to the exchange constant of oxygen as a reference substance for a system-independent parameter reaeration coefficients are often known for individual rivers and lakes. [Pg.218]

The drying rate is represented by differential equation (eq. 6) where h is mass transfer coefficient 1/(hcm ) , specific surface area of desiccant beads, cm /g mass of desiccant, g C, concentration by weight of water in the fluid being dried (7, concentration of water at the surface of the desiccant, ie, concentration of water in the fluid that would be in equihbrium with the instantaneous loading on the desiccant, wt-ppm and t — time, h. [Pg.509]

The required desiccant weight is a function of several factors the water removal requirements (mass/time), the cycle time, the equiUbrium loading of water on the desiccant at the feed conditions, the residual water loading on the desiccant after regeneration, and the size of the mass-transfer zone of the desiccant bed. These factors, in turn, depend on the flow rate, temperature, pressure, and water content of both the fluid being dried and the regeneration fluid (see Adsorption, gas separation). [Pg.516]


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See also in sourсe #XX -- [ Pg.195 , Pg.196 ]




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