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DESIGN OF PACKED TOWER
FOR LIQUID-LIQUID EXTRACTION
VIVEK J. PINGALE 641497
A PROJECT REPORT ON
GUIDED BY : Dr. Shashank G. Gaikwad Scientist, NCL , Pune
Liquid -Liquid ExtractionThe separation of the components of a liquid mixture by treatment with a solvent in whichone or more of the desired components is preferentially soluble is known as liquid–liquidExtraction.In all extraction processes, the important feature is the selective nature of the solvent,in that the separation of compounds is based on differences in solubility's, rather thandifferences in volatilities as in distillation.
Extraction is in many ways complementary to distillation
and is preferable in thefollowing cases
1. Where distillation would require excessive amounts of heat, such as, for example, when the relative volatility is near unity.
2. When the formation of azeotrope’s limits the degree of separation obtainable in distillation.
3. When heating must be avoided.4. When the components to be separated are quite
different in nature.
Three stages are involved
1. Bringing the feed mixture and the solvent into intimate contact.
2. Separation of the resulting two phases.3. Removal and recovery of the solvent from
each phase.
IN THE SINGLE-STAGE BATCH PROCESS ILLUSTRATED IN FIGURE
THE SOLVENT AND SOLUTION
ACETIC ACID+ WATER+ TOLUENE SYSTEM
•Composition Formation•Mixing•Stabilizing•Separating•Analyzing•Calculation
BATCH NO. Water in
gm
Acetic acid in
gm
Toluene in
gm
Batch-1 23 28 24
Batch-2 22 30 23
Batch-3 24 25 26
Batch-4 21 34 20
Batch-5 20 37 18
Batch-6 19 40 16
Batch-7 30 10 35
Batch-8 29 13 33
Batch-9 28 15 32
Batch-10 27 18 30
Batch-11 26 20 29
Batch-12 25 22 28
Batch-13 30 10 35
the toluene and acetic acid solution are mixed together and then allowed to separate into the two phases—the extract E containing the required solute in the added solvent and the raffinate R, the weaker solution with some associated solvent. With this simple arrangement, mixing and separation occurin the same vessel.
GENERAL SEPARATION PROCESS
APPLICATION OF LIQUID-LIQUID EXTRACTION
In the processing of coal tar liquids.In the production of fuels in the nuclear industry.To the separation of hydrocarbons in the petroleum industry.The separation of aromaticsfrom kerosene-based fuel oils to improve their burning quality.The separation of aromatics from paraffin and naphthenic compounds to improve the temperature-viscosity characteristics of lubricating oils.
It may also be used to obtain relativelypure compounds such as toluene from catalytically produced reformatesin the oil industry, in the production of anhydrous acetic acid, in the extraction ofphenol from coal tar liquors, and in the metallurgical and biotechnology industries.
PACKED TOWER
A packed tower is a hollow tube, pipe, or other vessel that is filled with packing material.
Two liquid phase are always present with contact.
Packing can randomly filled with small objects
The packing increases the interfacial area and increases mass transfer rates
Steady state mass transfer process
BASIC DATA FOR DESIGN Function Process material Steps involve for design of packed column Selection of packing Operating and design temperature and
pressure Material of construction Tower dimensions Opening and connections required Specification of internal fitting
FUNCTION Liquid-liquid, Liquid-vapor, Liquid-gas , Contact
Operations
STEPS INVOLVE FOR DESIGN OF PACKED COLUMN
Selection of packing Determine the column height Determine the column diameter packing support liquid distributor Check for pressure drop, liquid holdup,
and flooding.
SELECTION OF PACKING1) The Compounds are Temperature Sensitive2) Pressure Drop Is Important (Vacuum
Service)3) Liquid Loads are Low4) Towers are Small In Diameter5) Highly Corrosive Service (Use Plastic Or
Carbon)6) The System Is Foaming7) The Ratio of Tower Diameter To Random
Packing Is Greater Than 10.
TYPES OF PACKING MATERIAL
Raschig ring Lessing ring
Partition ring
Berl saddle
Intalox saddle
Tellerette Pall ring
PACKING MATERIALS
0.05 0.1 0.15 0.2 0.25 0.3 0.35 0.4 0.450
0.02
0.04
0.06
0.08
0.1
0.12
0.14
0.16
0.18
0.2
f(x) = 0.488204525774549 x − 0.0229504189507744R² = 0.995132253223116
Acetic Acid in Raffinate Phase
AA ORG.Linear (AA ORG.)Linear (AA ORG.)
GRAPH OF MOLE FRACTION OF ACETIC ACID IN EXTRACT PHASE VS. MOLE FRACTION OF ACETIC ACID IN ORGANIC PHASE
EXPERIMENTAL HTU DETERMINATON
The height of a transfer unit (HTU) is a measure of the separation effectiveness of the particular packing for a particular separation process.
Height of overall Transfer Unit, HTU is 3.396562707 m calculated by using slope m= 1.1965
EXPERIMENTAL NTU DETERMINATON
The number of transfer units (NTU) required is a measure of the difficulty of the separation
Number of a transfer unit (NTU) is 0.96122 calculated by using slope m= 1.1965
EXPERIMENTAL HEIGHT OF PACKING
Packing Height (Z) = Height of a Transfer Unit (HTU) X Number of a transfer unit (NTU)
Z = 3.396562707 m X 0.96122 =3.2648 m
0.06 0.08 0.1 0.12 0.14 0.16 0.18 0.20
0.02
0.04
0.06
0.08
0.1
0.12
0.14
0.16
0.18
0.2
f(x) = 1.055724552825 x − 0.0009970299391
NRTL
NRTL
Linear (NRTL)
NRTL graph for acetic acid
HTU DETERMINATON USING NRTL
The height of a transfer unit (HTU) is a measure of the separation effectiveness of the particular packing for a particular separation process.
Height of overall Transfer Unit, HTU is 1.430722756 m calculated by using slope m= 1.055
NTU DETERMINATON FOR NRTL
The number of transfer units (NTU) required is a measure of the difficulty of the separation.
Number of overall Transfer Unit, NTU is 3.01 calculated by using slope m= 1.055
NRTL HEIGHT OF PACKING
Packing Height (Z) = Height of a Transfer Unit (HTU) X Number of a transfer unit (NTU)
Z = 1.430722756 m X 3.01 =4.3077 m
DETERMINE THE COLUMN HEIGHT
Column height is calculated from HETP (Height Equivalent to Theoretical Plate)
Kx = liquid phase mass transfercoefficient
(X1*-X1) = driving force for MT of
raffinate phase
a= Interfacial area of packing
DETERMINE PACKING HEIGHTZ = N × H
where.,Z= packing heightN= number of transfer unit (NTU) -
dimensionlessH= height of transfer unit (HTU) – dimension
of length
COLUMN DIAMETER To handle the liquid and vapour flow Ratio of tower diameter to packing
diameter should usually be at least 15 Packed diameter is less 1/8th column
diameter. Use too large size in a small column can cause poor liquid distribution.
LIQUID DISTRIBUTOR
Perfect liquid distribution is defined asproviding equal liquid per unit area of thepacked bed surface.
• Orifice flow variation random, ± 5% to 6%• Head at minimum capacity, 2 inches• Light liquid risers have a 1 inch freeboard above max pool depth• Quiet liquid pool• Low horizontal liquid velocity, <1.25ft/s• Feed pipe discharge does not disrupt orifice flow• Orifice as large as possible
SUMMARY OF GOOD LIQUID DISTRIBUTOR DESIGN
PRESSURE DROP, LIQUID HOLDUP
& FLOODING. Packed towers almost always have
lower pressure drop compared to tray towers.
Generally packed towers are designed for 50% -- 85% flooding. If flooding is to be reduced,
Select larger packing size and repeat the above steps. OR
Increase the column diameter and repeat the above steps.
TOWER DIMENSIONS
Height Of Tower Was Estimated To be 3.26 m With Diameter of 0.163 m, Thickness of Tower Material 50 mm
Height Equivalent to Theoretical Stage (HETS) for liquid - liquid contacting is 0.4 - 0.56 m for in Bialechi rings.
Conclusion The final design includes significant
predicted improvements over the batch performance done in the lab. The design is based upon sound correlations as verified by the literature data consulted but still suffers from the cumulative propagation of small but significant error. While this was minimized by the careful selection of the correlations chosen, we have confidence in the numbers produced is cautiously estimated as ±20% and guessed to be as low as ±10%.
ACTUAL EXPERIMENTAL DESIGN OF PACKED COLUMN
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