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Mixing and Solution

Suppose now that the temperature Ti and absolute humidity m of the inlet air are specified, so that the state of the inlet air is fixed on the psychrometric chart. If we specify in addition the outlet air temperature T]( Ti), then m e/riia may be calculated from Equation 8.4-9, and it may in turn be used to calculate the absolute humidity of the outlet air. (m e + [Pg.395]

The outlet temperature and humidity determined in this manner are represented by a point on the psychrometric chart. If a lower value of Ts is assumed, a higher outlet humidity would be calculated, yielding another point on the chart. The set of ail such points for a specified and m i th defines a curve on the chart, known as the adiabatic saturation curve. If the three stated assumptions are valid, the final state of air undergoing an adiabatic humidification must lie on the adiabatic saturation curve that passes through the inlet state on the psychrometric chart. [Pg.395]

If the outlet temperature is low enough, the air leaves saturated with water. The temperature corresponding to this condition is called the adiabatic saturation temperature and is found at the intersection of the adiabatic saturation curve with the 100% relative humidity curve. [Pg.395]

YOURSELF abatic cooling follow a unique curve on the psychrometric chart, regardless of the [Pg.395]

Air at 26°C with a relative humidity of 10% undergoes an adiabatic humidification. Use [Pg.395]


Allison, J. A. et al., J. Amer. Chem. Soc., 1959, 81, 1089-1091 In absence of nitrogen as diluent, interaction with acetylene, cyclopropane or ethylene is explosive on mixing, and solutions in benzene explode on sparking or UV irradiation. [Pg.143]

In order for mixing and solution to occur, it is essential that the change in free energy, AG, which is the driving force in the solution process, decrease to below zero. A/f and AG are equal to the change in enthalpy and change in entropy, and for constant temperature the relationship is the classical Gibbs equation ... [Pg.51]

Attractive forces between nonpolar molecules such as mineral oil and n-hexane are very weak. Therefore, such molecules can mutually mix and solution is easy. The attractive forces between polar HjO or C H OH molecules are strong H-bonds. Most nonpolar molecules cannot overcome these H-bonds and therefore do not dissolve in such polar protic solvents. [Pg.22]

Taken from Landolt-Bbrnstein Numerical Data and Functional Relations in Science and Technology, New Series, Group IV, Vol. 2, Heats of Mixing and Solution, p. 492). [Pg.288]

Melt mixing and solution mixing methods were used to prepare short pineapple leaf fiber-LDPE composites. Effects of fiber length, content, and orientation on the mechanical properties have been studied. The mechanical properties were improved while the elongation at break was found to be reduced. Longitudinally oriented composites describe better properties compared to transversely and... [Pg.388]

This disadvantage does not apply to an isothermal device based on electrical compensation. Nevertheless, calorimeters of the latter type operate only in a quasi-isothermal mode, since electronic control systems depend for their response upon small deviations from an established set point, and a certain amount of time is required for changing the prevailing temperature. The use of modem circuits and components ensures that errors from this source will be negligible, however. Electrical compensation makes it possible to follow both endothermic and exothermic processes. In both cases the compensation power is readily measured and recorded or processed further with a computer. Isothermal calorimeters are used quite generally for determining heats of mixing and solution. Commercial devices are available that al.so support the precise work required for multiphase thermo-... [Pg.839]

Blends of NR with other polymers can be prepared by various mixing processes. Two main techniques, namely mechanical mixing and solution casting, have been widely used to produce NR polymer blends. The chemical bonding between NR and the blended polymers is not affected by the mixing method, but depends on their component types and concentrations. [Pg.200]

Both in melt-mixed and solution-cast systems, the viscosity decreased with increase of shear stress, indicating pseudoplastic behaviour (Figure 18.8). In both cases, negative and positive deviations in viscosity could be seen at a high and low shear rate. However, as compared to solution-casted blends, in melt-mixed ones, degradation of NR and PS due to high temperature and shear was... [Pg.421]

Property Type [HMSDl 111] HEAT OF MIXING AND SOLUTION ... [Pg.16]

Property Type [HMSDllll] HEAT OF MIXING AND SOLUTION State Two-component system, single-phase liquid or two-phase liquid-liquid (LL) Pure component 1, liquid Pure component 2, liquid Parameters 77K, Temperature Variables Xj/-, Mole fraction of component 1 //E/j mol-, Molar excess enthalpy Method Direct low-pressure calorimetric measurement of FP- at variable Xj and constant T ... [Pg.212]


See other pages where Mixing and Solution is mentioned: [Pg.409]    [Pg.51]    [Pg.409]    [Pg.193]    [Pg.395]    [Pg.395]    [Pg.397]    [Pg.399]    [Pg.401]    [Pg.403]    [Pg.405]    [Pg.48]    [Pg.237]    [Pg.59]    [Pg.252]    [Pg.28]    [Pg.771]    [Pg.213]    [Pg.1]    [Pg.213]    [Pg.214]    [Pg.215]    [Pg.219]   


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