Presentation on theme: "Solid – Liquid Extraction Prepared by Dr.Nagwa El-Mansy Chemical Engineering Department Cairo University."— Presentation transcript:
Solid – Liquid Extraction Prepared by Dr.Nagwa El-Mansy Chemical Engineering Department Cairo University
Solid-Liquid Extraction Solid liquid extraction(leaching) means the removal of a constituent from a mixture of solids by bringing the solid material into contact with a liquid solvent that dissolves this particular constituent. Applications:- 1- leaching of soybean oil from flaked soybeans with hexane. 2- Leaching of sugar from sugar beets with hot water.
3- Production of vegetable oils with organic solvents such as hexane, acetone and ether by extraction the oil peanuts, soybeans, sunflower seeds, cotton seeds and halibut livers. 4- Soluble tea is produced by water leaching of tea Leaves. 5- Gold is leached from its ore using an aqueous sodium cyanide solution. 6- Extraction of copper oxide from low grade ores with dilute H 2 SO 4 acid.
Mechanism of leaching:- Extraction involves two steps which are:- 1- Contacting step:- of solvent and the material to be Treated, so as to transfer soluble constituent to the Solvent. 2- Separation step:- of the solution formed from the relatively exhausted solids. The above two steps may be conducted in separate Equipment or in one and the same equipment. Solution resulting from separation step is termed Overflow, Solids left over are termed Underflow.
Extraction Terminology:- 1-Contacting Step:- Basically it’s a mass transfer step, it aims at transferring The soluble constituent from the solid phase into the liquid phase by diffusion and dissolution. The solute is first dissolved from the surface of the solid, then passes into the main body of the solution by diffusion. This process may result in the formation of pores in the solid material which exposes fresh(new) surfaces to subsequent solvent penetration to such surfaces.
An ideal contacting (mixing) stage yields a product in Thermodynamic Equilibrium→ No mass transfer. No heat transfer. No momentum transfer. Why its difficult to reach an ideal stage behavior, thermodynamic equilibrium ? * The rate of mass transfer is slow due to the pore resistance:- the rate of diffusion of solute out of the pores(capillaries) into the bulk solution are very slow. * Some part of the contained solute is not exposed to the solvent(inside a non-porous layer or closed pores).
* Sometimes the adsorption of the solute on the surface of the solid is > than the solubility in the solvent, so the realization of an ideal stage needs rather long times if the operations is carried out batch wise or an Excessively large apparatus if the operation is continuous. How to increase the rate of mass transfer? 1- Increase the agitation speed, thickness of the boundary Layer decreases. 2- As the temperature increase, the solubility increase, Hence, the diffusion increases, the viscosity decreases leading to decrease in the film thickness, hence the pore resistance decreases.
3-Size reduction of solid to increase the exposed mass transfer area. 2-Separation step:- This is a momentum transfer step that can be carried out by (settling or filtration). Calculations:- The design problem of calculating number of theoretical stages require simultaneous solution of material balance and equilibrium relations. We have three component system:- 1- solute (A) 2- Inert solid(B) 3- Solvent (S)
Representing the three component system on right angle triangle:-
Addition of two streams:-
Subtraction of two streams:-
Equilibrium Relations:- A-Locus of under flow:- 1- The mass of solution retained/unit mass of inert insoluble solids is obtained experimentally as a function of solution composition Y A. The data is usually available in tabular form. (Kg solution / Kg solids ) = (A+S)/BY A = ( A/ A+ S)
2- In some cases the solution retained/kg solids is approximated constant. i.e independent of composition. This means that the locus of underflow is a line parallel to the hypotenuse.
3 - Locus is a straight line:- Locus between two points ( 0, 0.8 ) & ( 0.4, 0 )
B- Locus of overflow:- Also the overflow consists generally of solution only,i.e (solid-free or inert-free) its locus is:- 1- The hypotenuse. 2- In some cases the overflow contains 10% solids and 90% solution. B : A + S 10 : 90 x B = B / ( A + B + S ) = 0.1
3- ………..and the overflow from the first stage contains 10% from the solids in the feed.
Ideal Extraction Stage:- Ideal extraction stage indicates whether or not we are close to thermodynamic equilibrium. The ideal stage in leaching is represented as a straight line going through point (B) and cutting the two locus in x 1 and y 1.
Methods of Operation (Types of contact):- 1-Simple single stage:- Considering a theoretical extraction stage where L 0 with composition x 0 is brought into contact with a solvent V 0 having composition y 0. The amount L 1 and Composition x 1 of the product underflow as well as the amount V 1 and comp. y 1 of the overflow are to be determined. determ
2- Multi-stage cross current contact:-
3- Multi-stage counter current contact:- Considering a feed with rate L 0 and composition x 0 which is to be treated with a solvent having a composition y n+1 at a rate of V n+1. The weight fraction in the U.F shouldn’t exceed a given value x nA.
To determine the number of ideal stages required to achieve this extraction duty use the following steps:- The overall M.B on the n stages may be written as:- * x 0, y n+1, and x n are located from the specifications of the problem. * x M, x 0 and y n+1 lies on the same straight line where x M Divides the distance between x 0 and y n+1 in the ratio of V n+1 / L 0.
M being the sum of L n and V 1, the points x n,x M,y 1 lies on one straight line. Hence y1 may be located by Extrapolating x n x M to meet the locus of the overflow.
Condition of infinite number of stages:- To increase overflow composition the number of stages must be increased. the number of stages increases till reaching the maximum overflow composition (y 1max ). Steps:- Connect y n+1 with (B) To cut U.F locus in x n min connect it with x M then extend the line to cut O.F in y 1max.
Stage Efficiency:- A deviation between the behavior of actual and Theoretical stages is expected. In theoretical stage:- (Solvent/ Solute) O.F = (Solvent/ Solute) U.F Actual stage is less efficient because:- 1- Slow rates of mass transfer resulting in unattainment of T.D.E (complete dissolution) in the contact time provided for the stage. 2-The solute is adsorbed by the solid to a higher content than the solvent.
3- The pore structure of the solid-solute mixture is such that only a portion of the solute is accessible to the solvent. Calculation of actual number of stages:- A- Construction when overflow efficiency is known:- The tie line representing an actual stage passes no Longer through the origin (B).
B- Construction when underflow efficiency is known:- The tie line representing an actual stage passes no Longer through the origin (B).
Solids-free coordinates:- The construction is in general less crowded than in the case of triangular diagram. No calculations are needed before plotting the equilibrium relations,but the same procedures described before are followed. The amounts of various streams should be expressed on solid-free basis. Some notes on Rectangular Diagram System:- The abscissa X (weight fraction of solute on a solid-free basis in the U.F) and Y (weight fraction of solute on a solid-free basis in the O.F) is plotted against the amount N (concentration of insoluble solids on the solid-free basis).
A typical equilibrium diagram is shown in the following Figure. The lower curve of N vs y A, where N = 0 on the axis, represents the locus of overflow(where all the solids has been removed). The upper curve N vs x A, Represents the locus of underflow. The tie lines are vertical, and on x-y diagram, the Equilibrium line is y A = x A
Types of contact:- (1)Simple Single Stage:-The application of material balance equations in conjunction with such diagram, the quantities of various streams should be expressed on solid-free basis. L 0 = mass of feed. = (A+B) or (A+B+S). L 0 ’= mass of feed on solid Free-basis = (A) or (A+S). V 0 = mass of solvent = (S+A) V 0 ’= mass of solvent on solid Free-basis = (S+A).
Single stage for the other type of equilibrium:-
3- Multi-stage counter current contact:-
Equipments in leaching:- 1- Fixed-bed leaching:-
Fixed bed leaching is used in the beet sugar and is also for extraction of pharmaceuticals from barks and seeds, and for other processes. In the Figure, the cover is removable so sugar beet slices can be dumped into the Bed. Hot water at 71 to 77 ◦ C flows into the bed to leach out the sugar. The leached sugar solution flows out the bottom onto the next tank in series. The top and bottom covers are removable so that the leached beets can be removed and a fresh charge added. About 95% Of the sugar in the beets is leached.
2-Bollman bucket-type extractor:-
Dry solids are added at the upper right side to a Perforated basket or bucket. The solid leached by a dilute solution called half miscella. The liquid downward through the moving buckets and is collected at the bottom as the strong solution or full miscella. The buckets moving upward on the left are leached counter currently by fresh solvent sprayed on the top bucket. The wet flasks are dumped as shown in the Figure and removed continuously.
3-Hildebrandt screw-conveyor extractor:-
Consists of three screw conveyers arranged in a U shape. The solids are charged at the top right conveyed downward, across the bottom, and then up the other Leg. The solvent flows counter currently to the solid.