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Liquid-Liquid Extractor Design
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Book: Handbook of Chemical Engineering Calculations

Modes of Operation: Cross-Current

Cross-current mode is mostly used in batch operation.  Batch extractors have traditionally been used in low capacity,
multi-product plants typically found in the pharmaceutical and agrochemical industries.   For washing and neutralization operations that require very few stages, cross-current operation is particularly practical and economical and offers a great deal of flexibility.  The extraction equipment usually includes an agitated tank that may also be used for the reaction steps.  In these tanks, the solvent is first added to the feed, the contents are mixed, settled, and then separated.   Single stage extraction is used when the extraction is fairly simple and can be achieved without a high amount of solvent.  If more than one stage is required, multiple solvent-washes will be required.

Though operation in cross-current mode a great deal of flexibility, it must be examined carefully due to the high solvent volume requirements and low extraction yields.  The following illustration gives a quick method to calculate solvent requirements for cross-current extraction.


A single-stage extractor can be represented as:

extrac30.gif (1636 bytes)

F = Feed quantity / rate, mass

R = Raffinate quantity / rate, mass

S = Solvent quantity / rate, mass

E = Extract quantity / rate, mass

 

Xf , X r, Y s, and Ye are the weight fractions of solute in the feed, raffinate, solvent and extract, respectively.

Partition coefficient ‘m’ is defined as the ratio of Ye to Xr at equilibrium conditions

The flows and concentrations are represented in solute-free basis as such a representation leads to simplification of equations. 

For example, for a 100 kg/hr feed containing 10% weight acetic acid, F = 100-10 = 90 kg/hr, Xr = 0.1/(1-0.1) = 0.111

 

The component mass balance can be represented as:

 F Xf + S Ys = R Xr + E Ye

Assuming (i) immiscibility of feed and solvent and (ii) the initial solvent is free of solute, i.e., F = R, S = E and Ys = 0 and using the equilibrium relation of Ye = m Xr, this equation simplifies to

 S = F/m (Xf /Xr–1)
Or
Reduction ratio, Xf /Xr = 1+ m S/F

For multi-stage crosscurrent operation:

extrac31.gif (2300 bytes)

Assuming that the partition coefficient (m) is constant over the concentration range and the solvent quantity in each of the ‘n’ stages is the same, i.e., S1 = S2 =…..=S n = S/n,

Solvent Requirement is

 S = n * F/m [(Xf /Xr)1/n - 1]
Or
Reduction ratio Xf /Xr = (1+mS/nF)n

It can be proved mathematically that the total solvent quantity would be minimum if the solvent were distributed equally between washes.

 

Reference: Optimize Liquid-Liquid Extraction, R. Madhaven, Cheresources.com

 


Modes of Operation: Counter-Current

As described above, the cross-current operation is mostly used in low capacity, multi-product, batch plants.  For larger volume operations, a counter-current configuration is often used.  Counter-current patterns are capable of more efficient use of the solvent.   Counter-current mixer-settlers or columns are usually employed.  Countercurrent operation conserves the mass transfer driving force thus they typically yield optimal performance.


extrac32.gif (2569 bytes)

Equations for countercurrent extraction get more complicated with increasing number of stages.  It can be shown that for a ‘n’ stage operation, the raffinate concentration would be

 Xr = Xf * (mS/F – 1)/ ( [mS/F] n+1 -1)
The solvent requirement for any raffinate concentration Xr could be determined by iteration from the above equation.

For mS/F = 1, the equation takes the form of Xr = Xf / (n + 1)

Reference: Optimize Liquid-Liquid Extraction, R. Madhaven, Cheresources.com


The dimensionless term mS/F, included in all the above equations, is called the extraction factor (E), and is an important parameter in the design of extraction processes.  For a given number of stages, the higher the E factor, the higher the reduction ratio thus a better extraction.  Systems with E of less than 1.3 are not likely to be commercially feasible.

Next > Operating Conditions and Solvents

Back to Start of Article

 


Rohit Ramesh Rewagad and Piyush Khatavkar
Bachelor of Technology in Chemical Eng.

Laxminarayan Institute of Technology, Nagpur India
Email: piyushkhatavkar ”at” gmail.com

 

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