6.Rate of absorption
First order rate equation of absorption
7.Relationship between flooding velocity(uf) and pressure (P)
Relationship between flooding velocity(uf) and pressure (P) of
1. Diffusion between two components
General diffusion equation between two components
2.Diffusion of component A into non diffusing B
For non-diffusing single component diffusion
3.Dependency of diffusivity on temperature and pressure
Diffusivity is directly proportional to temperature raise to power 1.5 and inversely proportional to pressure
4.Diffusivity in liquids
5.Equimolar counter current diffusion
Fick’s law of equimolar counter current diffusion
7.Mass transfer coefficient dependencies on diffusivity
Mass transfer coefficient dependencies on diffusivity according to various film theories
O2 is diffusing with non-diffusing gas (H2 and CH4), mean diffusivity is
Transient rate of diffusion into relatively thick mass of fluid with constant surface concentration. As exposure time decreases the mass transfer coefficient increases.
2.Surface Renewal theory
Surface renewal theory in Danckwert’s model of Mass transfer
S is also called fractional rate of surface renewal
14.Lewis Number and Psychromatic ratio
For air water system, Le = 1 = b; for air water system adiabatic saturation temperature = WBT
15. Stanton number (mass transfer)
The Sherwood number (Sh) (also called the mass transfer Nusselt number) represents the ratio of convective mass transfer to the rate of diffusive mass transport.Sherwood number is extensively used in convective mass
transfer calculations. Sherwood number for flow in a pipe can be expressed as the ratio of the concentration gradient at the surface to overall concentration difference. Forced convection is relatively more number which means mass transfer coefficient will be higher. Sherwood number for flow past flat plate
Sherwood number for flow in pipe can be expressed as the ratio of concentration gradient at surface to overall concentration difference. Sherwood number for flow past sphere in case of
2. Forced convection
17.Number of stages
Number of plates/stages for absorption, stripping and liquid-liquid extraction
No. of plates/stages for transfer of solute from liquid phase to vapor phase (stripping)
no. of plates/stages for transfer of solute from vapour phase to liquid absorption
3.Liquid – liquid extraction
All the boundary layers will coincide with each other when prandtl number = schmidt number = lewis number
20. Peclet number related to mass transfer
21. Normality and equivalent weight
22. Permeability of membrane
Relationship between permeability of membrane, solubility coefficient and diffusivity
23. For solubility related problem
For solubility related problem pertaining to mass transfer use the following equation
24. Liquid-liquid Extraction
In liquid-liquid extraction, Y = mX
25. Fractional holdup of gas bubbles (ϵ)
In a gas liquid contactor, fractional holdup of gas bubbles (ϵ) is defined as Interfacial area of bubble
2.Mass Transfer Theories
1. Degree of freedom in drying
Degree of freedom in drying – In drying of solids containing moisture above critical moisture content, no. of degree of freedom is F = C – P + 2
= 1 – 2 + 2 = 1.
2.Local efficiency and murphee efficiency
1. In small columns local efficiency is equal to Murphee efficiency. In large columns local efficiency is less than Murphee efficiency.
2. In a tray column, separating a binary mixture, with non – ideal stages, point efficiency cannot exceed 100% but Murphee efficiency can exceed 100%.
3.Towers and Columns
packed towers the gas is not bubbled through the liquid pool.
2.Plates column are preferred when operation involves liquid containing suspended solids. Plate columns are preferred when large temperature changes are involved in distillation operation. Packed towers are preferred if liquid has high foaming tendency. Packed towers are cheaper than plate towers if highly corrosive fluid is to be handled.
1.Gas – Gas diffusion coefficient is in order of 10^-5 m²/sec and liquid – liquid diffusion coefficient is in order of 10^-9 m²/sec.
2.For a given concentration difference, mass transfer flux for diffusion of only one component of mixture is greater than mass transfer flux of equimolal countercurrent diffusion.
3.Diffusivity will remain unaltered for both cases, stagnant and diffusing air.
4.Component A is diffusing in component B. The flux NA relative to a stationary point is equal to the flux due to molecular diffusion.
Roult’s law: The vapour pressure of a solution of a non-volatile solution is equal to vapour pressure of the pure solvent at that temperature multiplied by its mole fraction. P = Xsolute × Posolute.
In an ideal solution, it takes exactly the same amount of energy for a solvent molecule to break away from the surface of the solution as it did in pure solvent. The forces of attraction between solvent and solute are exactly the same as between the original solvent molecules.
Roult’s law only works for solutes which doesn’t change their nature when they dissolve, i.e. they mustn’t ionize or associate. Remember: vapour pressure is inversely proportional to boiling point.
Positive deviation from roult’s law In mixtures showing positive deviation from roult’s law, the vapour pressure of the mixture is always higher than you would expect from an ideal mixture. If a mixture has a high vapour pressure it means that it will have a low boiling point. The molecules are escaping easily and one won’t have to heat the mixture much to overcome the intermolecular attractions completely. Negetive deviation from roult’s law Mixture have vapour pressure which is less than would be expected by roult’s law. Minimum value for vapour pressure would be lower
6. Dimensionless numbers Mass transfer
1.At temperature 750K and 1 atm pressure the approximate value of Schmidt number for air is 0.1.
2.Schmidt number is independent of pressure when ideal gas law applies as effect of pressure on density and diffusivity cancel each other and viscosity is independent of pressure.
3.Boundary layer theory is for laminar flow only and Schmidt number is equal to one in this theory.
1.The ΔL law of crystal growth: If all crystals in magma grow in a uniform super saturation field and at the same temperature and if all the crystals grow from birth at rate governed by super saturation, then all crystals are not only in variant but also have the same growth rate that is independent of size ΔL = G Δt. The total growth of each crystals in the magma during the same time interval Δt is the same.
2.A supersaturated solution of a sparingly soluble solute, at a concentration C is being fed to a crystallizer at volumetric flow rate of V. The solubility of solute is Cs. The output rate of solids from efficient crystallizer is (C – Cs)/V.
8. Distillation and Absorption
1.Increasing the L/V ratio increases driving force everywhere in the column except at the top of the column.
2.Reflux is added in distillate column in order to increase the concentration of the more volatile component in the distillate. If no reflux is added to the top plate, enrichment is not possible and the composition of the distillate would be same as that of original feed.
3.The boiling point of a mixture of two immiscible liquids is always less than the boiling point of each individual component.
5.In case of steam distillation, less number of trays are required as compared to during usage of reboiler.
6.A distillation column at a pilot plant is scaled up by n times for industrial use at steady state. Then number of theoretical trays doesn’t increase n times, minimum reflux doesn’t increase by n times, feed flow rate and product flow rate are increased by n times, feed composition and product composition doesn’t increase by n times.
9. Operating line and equilibrium line
1. Any point on the operating line expresses the material balance equation for the transferring component between top and bottom part of packed tower. The vertical distance between operating line and equilibrium line represents the driving force for mass transfer at a particular point inside tower.
1.In a few extraction systems, the direction of tie line slope changes and one tie line will be horizontal. Such systems are said to be solutropic system. It is involved in liquid-liquid extraction.
2.The commonly used solvent in supercritical extraction is carbon dioxide.
1. Apparent activation energy in case of adsorption Ea = E – ΔHads
12. Mass transfer theories
1. Surface renewal theory and penetration theory is for unsteady state conditions. Boundary layer theory and film theory is for steady state conditions.