The document discusses liquid-liquid extraction as a separation technique. It provides three main points:
1. Liquid-liquid extraction separates species according to differences in solubility between two immiscible liquids, rather than volatility as in distillation.
2. The key components in liquid-liquid extraction are a solute, solvent, and inert components that form two separate liquid phases - an extract and raffinate.
3. There are two main types of systems - one forming one pair of partially miscible liquids leading to a closed ternary diagram, and one forming two pairs forming an open ternary diagram.
The document then discusses various aspects of setting up counter-current multi-
Vacuum distillation allows purification of compounds that cannot be readily distilled under normal atmospheric pressure or that may decompose at high temperatures. It works by reducing pressure above the boiling liquid, lowering the boiling point so compounds evaporate and separate based on differences in their boiling points. Key advantages are faster processing, ability to distill higher boiling point solvents without damage, and improved separation, yield, and purity. It finds applications in separating thermolabile substances and preparing extracts while preserving active constituents.
This document discusses face powders, including their ideal properties, ingredients, manufacturing processes, and evaluation. It covers both loose and compact face powders. Key points include:
- The main ingredients in loose face powders are talc, kaolin, chalk, zinc oxide, and titanium dioxide. Binders like stearates are also used.
- Compact powders use binding agents like stearates, oils, gums, or emulsions to form cakes that are compressed.
- Loose powders are mixed and sifted by hand or machine. Compact powders can be made by wet molding, damp compression, or dry compression in mechanical presses.
- Properties of face
1. The document discusses multistage separation processes and different types of distillation operations including simple distillation, flash distillation, and multistage distillation.
2. Simple distillation involves a feed, distillate, and residue stream, and can be solved graphically or algebraically using material balances.
3. Flash distillation separates a feed stream into a vapor and liquid product using equilibrium relationships, and the compositions are solved using operating line equations.
4. Examples show how to apply material balances and equilibrium relationships to calculate stream compositions for simple and flash distillation problems.
This document describes the process of saponification to produce soap. Key steps include:
1) Boiling fats or oils with a concentrated alkali solution like sodium hydroxide or potassium hydroxide to hydrolyze the oils into fatty acids and glycerol.
2) Neutralizing the fatty acids produced with additional alkali to form soap, which is then separated, washed, and dried.
3) The procedure involves boiling palm oil with sodium hydroxide solution, adding water and sodium chloride, cooling and filtering to obtain solid soap, then testing the soap.
The students measured the surface area of charcoal using the adsorption of acetic acid. They titrated solutions with varying concentrations of acetic acid exposed to charcoal to determine the equilibrium concentration and moles of acid adsorbed per gram of charcoal. Plotting these values showed they were directly proportional, allowing the students to determine the monolayer capacity from the slope. Using this monolayer capacity, the students calculated the surface area of the charcoal to be 657.35±20.22 m2/g, which was within 48% of the literature value. The adsorption was found to follow the Langmuir isotherm model of adsorption on a homogeneous surface.
When phases exist together, the boundary between two of them is known as interface.
When the phase is in contact with atmosphere it is termed as surface.
Vacuum distillation allows purification of compounds that cannot be readily distilled under normal atmospheric pressure or that may decompose at high temperatures. It works by reducing pressure above the boiling liquid, lowering the boiling point so compounds evaporate and separate based on differences in their boiling points. Key advantages are faster processing, ability to distill higher boiling point solvents without damage, and improved separation, yield, and purity. It finds applications in separating thermolabile substances and preparing extracts while preserving active constituents.
This document discusses face powders, including their ideal properties, ingredients, manufacturing processes, and evaluation. It covers both loose and compact face powders. Key points include:
- The main ingredients in loose face powders are talc, kaolin, chalk, zinc oxide, and titanium dioxide. Binders like stearates are also used.
- Compact powders use binding agents like stearates, oils, gums, or emulsions to form cakes that are compressed.
- Loose powders are mixed and sifted by hand or machine. Compact powders can be made by wet molding, damp compression, or dry compression in mechanical presses.
- Properties of face
1. The document discusses multistage separation processes and different types of distillation operations including simple distillation, flash distillation, and multistage distillation.
2. Simple distillation involves a feed, distillate, and residue stream, and can be solved graphically or algebraically using material balances.
3. Flash distillation separates a feed stream into a vapor and liquid product using equilibrium relationships, and the compositions are solved using operating line equations.
4. Examples show how to apply material balances and equilibrium relationships to calculate stream compositions for simple and flash distillation problems.
This document describes the process of saponification to produce soap. Key steps include:
1) Boiling fats or oils with a concentrated alkali solution like sodium hydroxide or potassium hydroxide to hydrolyze the oils into fatty acids and glycerol.
2) Neutralizing the fatty acids produced with additional alkali to form soap, which is then separated, washed, and dried.
3) The procedure involves boiling palm oil with sodium hydroxide solution, adding water and sodium chloride, cooling and filtering to obtain solid soap, then testing the soap.
The students measured the surface area of charcoal using the adsorption of acetic acid. They titrated solutions with varying concentrations of acetic acid exposed to charcoal to determine the equilibrium concentration and moles of acid adsorbed per gram of charcoal. Plotting these values showed they were directly proportional, allowing the students to determine the monolayer capacity from the slope. Using this monolayer capacity, the students calculated the surface area of the charcoal to be 657.35±20.22 m2/g, which was within 48% of the literature value. The adsorption was found to follow the Langmuir isotherm model of adsorption on a homogeneous surface.
When phases exist together, the boundary between two of them is known as interface.
When the phase is in contact with atmosphere it is termed as surface.
This document discusses cosmetic chemistry concepts including atoms, molecules, elements, compounds, mixtures, pH, acidity, alkalinity, and the acid mantle. It then covers how cosmetics can be classified based on their physical and chemical properties, including powders, suspensions, ointments, solutions, emulsions, and soaps. Specific examples are provided for each classification. Makeup products like face powder and foundation are also briefly discussed.
Slides for the eLearning course Separation and purification processes in biorefineries (https://open-learn.xamk.fi) in IMPRESS project.
Section: Distillation
Subject: 1.1 Vapor Liquid Equilibrium
The McCabe-Thiele method is a graphical technique for determining the minimum number of stages required for distillation. It involves plotting the equilibrium relationship between liquid and vapor phases on a diagram and constructing operating lines to represent the mass balances in the rectifying and stripping sections. Intersections between the lines indicate the number of ideal stages. The method was developed in 1925 and remains useful for preliminary column design. Key considerations include the feed composition and enthalpy, reflux ratio, and use of partial condensers or reboilers.
This document provides examples of calculating fugacity coefficients and activity coefficients for mixtures using various equations of state and activity coefficient models. It gives the equations and steps to estimate fugacity coefficients for species in mixtures using the Redlich-Kwong and virial equations of state, as well as fugacity coefficients for pure components using correlations. It also demonstrates calculating activity coefficients for solutions using the Van Laar, regular solution, and UNIFAC models by given the necessary parameters and mole fractions.
This document provides information about azeotropic distillation prepared by Claire E. Canoy for their 2nd year Chemical Engineering Technology course. It defines azeotropic distillation as adding an entrainer component to a feed mixture to form a new azeotrope that can be separated into its components by distillation. The entrainer allows either the separation of a closely boiling pair or the separation of an azeotrope into its components. A diagram shows the process of mixing the feed and entrainer before distillation in two columns to separately remove the key components and recycle the entrainer.
Distillation is a method of separating mixtures based on differences in volatility. It involves heating a mixture to vaporize components with lower boiling points and then condensing the vapors. There are several types of distillation including simple distillation, fractional distillation, steam distillation, and destructive distillation. Fractional distillation uses a fractionating column with multiple theoretical plates to achieve high purity separations, while steam distillation uses steam to lower boiling points of heat-sensitive materials. Distillation is an important separation technique used in pharmacy, chemistry, and other fields.
Vacuum distillation is used in oil refineries to further separate and refine the bottoms leftover from atmospheric distillation. It allows for distillation of compounds with high boiling points without thermal cracking by reducing the pressure and lowering the boiling points. Vacuum distillation units in refineries can have columns up to 14 meters wide and 50 meters tall, processing up to 25,400 cubic meters of feed per day. This additional refinement produces more valuable petroleum products from the heavier fractions of crude oil.
This document discusses ideal and non-ideal solutions. An ideal solution obeys Raoult's law over the entire concentration range and has no change in enthalpy or volume on mixing. Non-ideal solutions deviate from Raoult's law and can have positive or negative changes in enthalpy and volume. Solutions with positive deviations have weaker intermolecular forces between components, while those with negative deviations have stronger intermolecular forces. Azeotropes are solutions that boil at a constant temperature, with the liquid and vapor phases having the same composition. Minimum boiling azeotropes have very large positive deviations, while maximum boiling azeotropes show negative deviations from Raoult's law.
Slides for the eLearning course Separation and purification processes in biorefineries (https://open-learn.xamk.fi) in IMPRESS project (https://www.spire2030.eu/impress).
Section: Distillation
Subject: 1.2 Flash distillation.
Soaps are made by reacting fats or oils with a strong alkali like sodium hydroxide. Detergents are similar cleansing agents but use synthetic surfactants instead of fats/oils and do not form scum with hard water. The manufacturing process for soaps involves saponification of fats/oils, glycerin removal, purification, and finishing. Detergent production uses petrochemical raw materials and involves slurry making and spray drying. Both have advantages like cleaning ability but can harm aquatic environments if not properly treated in wastewater.
The document discusses the soap making process which includes:
1) Mixing oils and lye to saponify and create soap
2) Pouring the mixture into molds and allowing it to dry
3) Cutting the dried soap into bars once removed from molds
It also provides tips on selecting oils for different properties in soap and calculating the amount of lye needed based on the oils used.
This document summarizes a student project report on the preparation of soap. It defines soap and discusses its history. It outlines the raw materials used like sodium hydroxide, potassium hydroxide, oils, and extracts. It describes the processes of saponification and different soap making methods. It also covers types of soaps, examples with total fatty matter percentages, safety considerations, and conclusions.
This document discusses leaching processes and equipment. Leaching involves using a liquid solvent to selectively dissolve components from a solid mixture. It is widely used in industries such as food processing, metals extraction, and pharmaceuticals. Countercurrent leaching systems are described that allow for efficient extraction through multiple stages with fresh solvent added and concentrated solutions removed counter to the direction of solids movement. Specific leaching equipment discussed include the Kennedy extractor, continuous countercurrent decantation system, Bollman extractor, and Rotocell extractor. Mass balances are provided for single and multistage countercurrent leaching systems.
1) Material balances apply the law of conservation of mass to chemical processes, ensuring mass is neither created nor destroyed.
2) To perform a material balance, a process flow diagram is drawn with stream labels and unknowns assigned symbols. A basis is selected before writing balance equations.
3) For reactive systems, stoichiometric ratios from chemical equations are used in material balances to determine limiting reactants and calculate yields, selectivity, and conversion.
Distillation is a method of separating mixtures based on differences in volatility. It involves heating a mixture to vaporize components with lower boiling points and then condensing the vapors. There are several types of distillation including simple distillation, fractional distillation, steam distillation, and destructive distillation. Fractional distillation uses a fractionating column with multiple theoretical plates to achieve high purity separations, while steam distillation uses steam to lower boiling points of heat-sensitive materials. Distillation is an important separation technique used in pharmacy, chemistry, and other fields.
1) Distillation is a method used to separate components of a liquid solution based on differences in how the components distribute between the vapor and liquid phases when heated to their boiling points.
2) Raoult's law describes vapor-liquid equilibrium for ideal solutions, relating the partial pressure of a component in vapor phase to its mole fraction in the liquid phase. Boiling point diagrams can be constructed using vapor pressure data.
3) Equilibrium or flash distillation involves heating a liquid mixture to partially vaporize it in a single stage, separating the vapor and liquid which approach equilibrium compositions.
Slides for the eLearning course Separation and purification processes in biorefineries (https://open-learn.xamk.fi) in IMPRESS project (https://www.spire2030.eu/impress).
Subject: 2.4 Plate efficiencies.
This document discusses liquid-liquid extraction with an intermediate feed. It provides several equations to model systems with an intermediate feed, including mass balances around stages where the feed is introduced. It also shows schematics of typical equilibrium stage diagrams for such systems. Key points covered include that each feed should be introduced at the proper stage, and equations relate compositions in different stages and feeds.
This document discusses liquid-liquid extraction with an intermediate feed. It provides several equations to model systems with an intermediate feed entering at a particular stage. When there are multiple feeds, they can either be separated in individual apparatuses, mixed and fed together, or each introduced at the proper stage of the same apparatus. Diagrams show the stages, flows, compositions and equilibrium relationships for systems with an intermediate feed. The document also discusses some special cases like when the solvent is fully recovered or under total reflux conditions.
This document discusses cosmetic chemistry concepts including atoms, molecules, elements, compounds, mixtures, pH, acidity, alkalinity, and the acid mantle. It then covers how cosmetics can be classified based on their physical and chemical properties, including powders, suspensions, ointments, solutions, emulsions, and soaps. Specific examples are provided for each classification. Makeup products like face powder and foundation are also briefly discussed.
Slides for the eLearning course Separation and purification processes in biorefineries (https://open-learn.xamk.fi) in IMPRESS project.
Section: Distillation
Subject: 1.1 Vapor Liquid Equilibrium
The McCabe-Thiele method is a graphical technique for determining the minimum number of stages required for distillation. It involves plotting the equilibrium relationship between liquid and vapor phases on a diagram and constructing operating lines to represent the mass balances in the rectifying and stripping sections. Intersections between the lines indicate the number of ideal stages. The method was developed in 1925 and remains useful for preliminary column design. Key considerations include the feed composition and enthalpy, reflux ratio, and use of partial condensers or reboilers.
This document provides examples of calculating fugacity coefficients and activity coefficients for mixtures using various equations of state and activity coefficient models. It gives the equations and steps to estimate fugacity coefficients for species in mixtures using the Redlich-Kwong and virial equations of state, as well as fugacity coefficients for pure components using correlations. It also demonstrates calculating activity coefficients for solutions using the Van Laar, regular solution, and UNIFAC models by given the necessary parameters and mole fractions.
This document provides information about azeotropic distillation prepared by Claire E. Canoy for their 2nd year Chemical Engineering Technology course. It defines azeotropic distillation as adding an entrainer component to a feed mixture to form a new azeotrope that can be separated into its components by distillation. The entrainer allows either the separation of a closely boiling pair or the separation of an azeotrope into its components. A diagram shows the process of mixing the feed and entrainer before distillation in two columns to separately remove the key components and recycle the entrainer.
Distillation is a method of separating mixtures based on differences in volatility. It involves heating a mixture to vaporize components with lower boiling points and then condensing the vapors. There are several types of distillation including simple distillation, fractional distillation, steam distillation, and destructive distillation. Fractional distillation uses a fractionating column with multiple theoretical plates to achieve high purity separations, while steam distillation uses steam to lower boiling points of heat-sensitive materials. Distillation is an important separation technique used in pharmacy, chemistry, and other fields.
Vacuum distillation is used in oil refineries to further separate and refine the bottoms leftover from atmospheric distillation. It allows for distillation of compounds with high boiling points without thermal cracking by reducing the pressure and lowering the boiling points. Vacuum distillation units in refineries can have columns up to 14 meters wide and 50 meters tall, processing up to 25,400 cubic meters of feed per day. This additional refinement produces more valuable petroleum products from the heavier fractions of crude oil.
This document discusses ideal and non-ideal solutions. An ideal solution obeys Raoult's law over the entire concentration range and has no change in enthalpy or volume on mixing. Non-ideal solutions deviate from Raoult's law and can have positive or negative changes in enthalpy and volume. Solutions with positive deviations have weaker intermolecular forces between components, while those with negative deviations have stronger intermolecular forces. Azeotropes are solutions that boil at a constant temperature, with the liquid and vapor phases having the same composition. Minimum boiling azeotropes have very large positive deviations, while maximum boiling azeotropes show negative deviations from Raoult's law.
Slides for the eLearning course Separation and purification processes in biorefineries (https://open-learn.xamk.fi) in IMPRESS project (https://www.spire2030.eu/impress).
Section: Distillation
Subject: 1.2 Flash distillation.
Soaps are made by reacting fats or oils with a strong alkali like sodium hydroxide. Detergents are similar cleansing agents but use synthetic surfactants instead of fats/oils and do not form scum with hard water. The manufacturing process for soaps involves saponification of fats/oils, glycerin removal, purification, and finishing. Detergent production uses petrochemical raw materials and involves slurry making and spray drying. Both have advantages like cleaning ability but can harm aquatic environments if not properly treated in wastewater.
The document discusses the soap making process which includes:
1) Mixing oils and lye to saponify and create soap
2) Pouring the mixture into molds and allowing it to dry
3) Cutting the dried soap into bars once removed from molds
It also provides tips on selecting oils for different properties in soap and calculating the amount of lye needed based on the oils used.
This document summarizes a student project report on the preparation of soap. It defines soap and discusses its history. It outlines the raw materials used like sodium hydroxide, potassium hydroxide, oils, and extracts. It describes the processes of saponification and different soap making methods. It also covers types of soaps, examples with total fatty matter percentages, safety considerations, and conclusions.
This document discusses leaching processes and equipment. Leaching involves using a liquid solvent to selectively dissolve components from a solid mixture. It is widely used in industries such as food processing, metals extraction, and pharmaceuticals. Countercurrent leaching systems are described that allow for efficient extraction through multiple stages with fresh solvent added and concentrated solutions removed counter to the direction of solids movement. Specific leaching equipment discussed include the Kennedy extractor, continuous countercurrent decantation system, Bollman extractor, and Rotocell extractor. Mass balances are provided for single and multistage countercurrent leaching systems.
1) Material balances apply the law of conservation of mass to chemical processes, ensuring mass is neither created nor destroyed.
2) To perform a material balance, a process flow diagram is drawn with stream labels and unknowns assigned symbols. A basis is selected before writing balance equations.
3) For reactive systems, stoichiometric ratios from chemical equations are used in material balances to determine limiting reactants and calculate yields, selectivity, and conversion.
Distillation is a method of separating mixtures based on differences in volatility. It involves heating a mixture to vaporize components with lower boiling points and then condensing the vapors. There are several types of distillation including simple distillation, fractional distillation, steam distillation, and destructive distillation. Fractional distillation uses a fractionating column with multiple theoretical plates to achieve high purity separations, while steam distillation uses steam to lower boiling points of heat-sensitive materials. Distillation is an important separation technique used in pharmacy, chemistry, and other fields.
1) Distillation is a method used to separate components of a liquid solution based on differences in how the components distribute between the vapor and liquid phases when heated to their boiling points.
2) Raoult's law describes vapor-liquid equilibrium for ideal solutions, relating the partial pressure of a component in vapor phase to its mole fraction in the liquid phase. Boiling point diagrams can be constructed using vapor pressure data.
3) Equilibrium or flash distillation involves heating a liquid mixture to partially vaporize it in a single stage, separating the vapor and liquid which approach equilibrium compositions.
Slides for the eLearning course Separation and purification processes in biorefineries (https://open-learn.xamk.fi) in IMPRESS project (https://www.spire2030.eu/impress).
Subject: 2.4 Plate efficiencies.
This document discusses liquid-liquid extraction with an intermediate feed. It provides several equations to model systems with an intermediate feed, including mass balances around stages where the feed is introduced. It also shows schematics of typical equilibrium stage diagrams for such systems. Key points covered include that each feed should be introduced at the proper stage, and equations relate compositions in different stages and feeds.
This document discusses liquid-liquid extraction with an intermediate feed. It provides several equations to model systems with an intermediate feed entering at a particular stage. When there are multiple feeds, they can either be separated in individual apparatuses, mixed and fed together, or each introduced at the proper stage of the same apparatus. Diagrams show the stages, flows, compositions and equilibrium relationships for systems with an intermediate feed. The document also discusses some special cases like when the solvent is fully recovered or under total reflux conditions.
The document discusses linear transformations and linear independence. It contains examples and explanations of:
1) How a matrix A can transform a vector x from R4 to a new vector b in R2, representing the linear transformation.
2) How finding vectors x such that Ax=b is equivalent to finding pre-images of b under the transformation A.
3) Key concepts related to linear transformations like domain and range.
The result is incorrect as sign extension was not considered. For signed multiplication, sign extension of operands is required before performing multiplication as for unsigned numbers.
Signed Multiplication (contd..)
For signed multiplication:
Extend the sign bit of both operands to fill the register.
Perform multiplication as for unsigned numbers.
The final product now represents a signed number in 2's complement form.
Example: (-13) × (+11)
-13 in 2's complement is 1 0 0 1 1
+11 in 2's complement is 0 1 0 1 1
After sign extension:
-13 = 1 1 1 1 1
Graphs are used in physics to show relationships between variables. A linear graph indicates a direct proportional relationship between variables. The slope of a linear graph is calculated by taking the rise over the run and represents the ratio of change in the dependent variable to the change in the independent variable. For nonlinear relationships, manipulating the variables, such as squaring or taking reciprocals, can linearize the relationship. The slope of the resulting linear graph then represents a physical quantity defined by the original equation.
This document discusses Fourier series and their application to solving partial differential equations that model transport phenomena. Specifically, it provides:
1) An overview of Fourier series and their use in expanding periodic functions as an infinite sum of sines and cosines.
2) An example of using Fourier series to solve the one-dimensional transient heat conduction equation, resulting in an infinite series solution for the dimensionless temperature.
3) Details on the steps of the Fourier series solution method, including separating variables, applying boundary conditions, and determining coefficients to obtain the series solution.
1) Laplace's equation describes situations where the electric potential (V) or other scalar field satisfies ∇^2V = 0. It can be solved in one, two, or three dimensions using separation of variables.
2) In three dimensions, the general solution is a sum of multipole terms involving associated Legendre polynomials. The leading terms are the monopole and dipole contributions.
3) For a dipole potential, the electric field is proportional to p/r^3 where p is the dipole moment. The field points radially away from a head-to-tail dipole and has no φ dependence.
Comparison Of Dengue Cases Between Chosen District In Selangor By Using Fouri...Mohd Paub
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This document discusses various datapath subsystems including shifters and multipliers. It describes barrel shifters and logarithmic shifters, noting that barrel shifters have O(N^2) transistors while logarithmic shifters have O(NlogN) transistors. For multipliers, it explains how a basic array multiplier works by forming partial products and summing them, and notes the critical paths involve the full adders in the top row. It also introduces carry save multipliers for faster multiplication.
IMPACT Silver is a pure silver zinc producer with over $260 million in revenue since 2008 and a large 100% owned 210km Mexico land package - 2024 catalysts includes new 14% grade zinc Plomosas mine and 20,000m of fully funded exploration drilling.
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Starting a business is like embarking on an unpredictable adventure. It’s a journey filled with highs and lows, victories and defeats. But what if I told you that those setbacks and failures could be the very stepping stones that lead you to fortune? Let’s explore how resilience, adaptability, and strategic thinking can transform adversity into opportunity.
The Genesis of BriansClub.cm Famous Dark WEb PlatformSabaaSudozai
BriansClub.cm, a famous platform on the dark web, has become one of the most infamous carding marketplaces, specializing in the sale of stolen credit card data.
Prescriptive analytics BA4206 Anna University PPTFreelance
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The APCO Geopolitical Radar - Q3 2024 The Global Operating Environment for Bu...APCO
The Radar reflects input from APCO’s teams located around the world. It distils a host of interconnected events and trends into insights to inform operational and strategic decisions. Issues covered in this edition include:
Unveiling the Dynamic Personalities, Key Dates, and Horoscope Insights: Gemin...my Pandit
Explore the fascinating world of the Gemini Zodiac Sign. Discover the unique personality traits, key dates, and horoscope insights of Gemini individuals. Learn how their sociable, communicative nature and boundless curiosity make them the dynamic explorers of the zodiac. Dive into the duality of the Gemini sign and understand their intellectual and adventurous spirit.
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During the budget session of 2024-25, the finance minister, Nirmala Sitharaman, introduced the “solar Rooftop scheme,” also known as “PM Surya Ghar Muft Bijli Yojana.” It is a subsidy offered to those who wish to put up solar panels in their homes using domestic power systems. Additionally, adopting photovoltaic technology at home allows you to lower your monthly electricity expenses. Today in this blog we will talk all about what is the PM Surya Ghar Muft Bijli Yojana. How does it work? Who is eligible for this yojana and all the other things related to this scheme?
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4. WHY LIQUID-LIQUID EXTRACTION
When nearly equal 1.
For azeotropic mixtures.
To avoid thermal decomposition.
Some notes:
1- Separation is done according to different in solubility
(not volatility).
2- Problem with L-L extraction that we mix then we
separate.
5. WHAT IS LIQUID-LIQUID EXTRACTION
Species involved: Vo: Mass flow rate of fresh solvent.
yo: Mass fraction of solute in solvent
Solute + Inert
Lo: Mass flow rate of liquid feed mixture
Solvent
xo: Mass fraction of solute in meal
Each stage contain: V1: Mass flow rate of Extract layer
Contact y1: Mass fraction of solute in Extract
Separation L1: Mass flow rate of Raffinate layer
x1: Mass fraction of solute in Raffinate
Solvent Extract
Vo, yo V1, y1
Contact Separation
Feed Raffinate
Lo, xo L1, x1
7. TYPES OF TERNARY SYSTEMS
Formation of one pair of partially miscible liquids.
[closed ternary diagram]
Formation of two pair of partially miscible liquids.
[open ternary diagram]
8. FORMATION OF ONE PAIR OF PARTIALLY
MISCIBLE LIQUIDS
AS&BS are completely soluble.
S
AB is partially soluble.
M will be separated to two
compositions; N & L I
If S is solvent for A so as S P
increases, L goes up till P(Plait
Point) at which A,B & S become
one phase. This is done due to L
the increase in mutual solubility
between A&B. N
M
II
A B
9. FORMATION OF ONE PAIR OF PARTIALLY
MISCIBLE LIQUIDS
Equilibrium relation.
y
P
x
10. FORMATION OF TWO PAIR OF PARTIALLY
MISCIBLE LIQUIDS
S
AS&AB are partially soluble.
B is completely soluble in S. I
y
I II
A B
x
11. STAGE DEFINITION
It is a mechanical device or series that allow the
solvent & solution to contact and separate. So;
stage is:
12. S y0
SINGLE STAGE
y1
V0, y0 V1, y1
M
L0, x0 1 L1, x1
x1
x0
B A
y
V0+L0=V1+L1=M
V0y0+L0x0=V1y1+L1x1=MxM
y0, x0, xM are on the same straight line
y1, x1, xM are on the same straight line
x
13. S y0
MULTI STAGE CROSS CURRENT
y2
V0, y0 V0, y0 y1
M2
M1
L0, x0 L1, x1 L2, x2 x2 x
1 2 1
x0
B A
y
V1, y1 V2, y2
are y0, x0, xM1 are on the same straight line
y1, x1, xM1 on the same straight line
are y0, x1, xM2 are on the same straight line
y2, x2, xM2 on the same straight line
x
14. S yn+1
MULTI STAGE COUNTER CURRENT
y3
y2
M y1
V1, y1 Vn, yn Vn+1, yn+1
xn x3 x x
1 n 2 1
x0
B A
L0, x0 L1, x1 Ln, xn
y
Vn+1+L0=V1+Ln=M
Vn+1yn+1+L0x0=V1y1+Lnxn=MxM
yn+1
L0-V1=Ln-Vn+1=R R
No. of stages= n+(a/a+b)
But get a & b from AB line
xn+1 b a
xn-1
xn x
15. S yn+1
PROJECTION OF OPERATING LINE
M y1
xn
x0
B A
y
R
Equilibrium
Operating
x
16. EXTRACT & RAFFINATE EFFICIENCY
y y
Equilibrium Equilibrium
H L
0.9H
0.8L
New
Equilibrium
New
Equilibrium
Operating Operating
x x
Extract efficiency 90% Raffinate efficiency 80%
17. PROBLEM (1)
Givens:
A counter current-multi stage system.
We need to recover Pyridine from aqueous solution by Chloro-
benzene.
xn=0.01
x0=0.25
Vn+1/L0=10
Required:
1. Maximum pyridine content that may be obtained in the
extract phase leaving the system.
For ratio of solvent to feed of 10 determine:
1. Composition and quantity (expressed as pounds per pound
of feed) of extract phase leaving the system.
2. The number of equilibrium stages required.
18. PROBLEM (1)
Raffinate layer Extract layer
Chloro- Chloro-
Pyridine Water Pyridine Water
benzene benzene
xA xB xS yA yB yS
0.25 0.73 0.02 0.28 0.03 0.69
0.12 0.88 0 0.18 0.02 0.8
0.03 0.97 0 0.07 0.02 0.91
0.01 0.99 0 0.03 0.01 0.96
19. S yn+1
PROBLEM (1)
Raffinate Extract
Raffinate layer Extract layer B x0
Chloro- Chloro-
xn A
Pyridine Water
benzene
Pyridine Water
benzene yA
xA xB xS yA yB yS
0.25 0.73 0.02 0.28 0.03 0.69
0.12 0.88 0 0.18 0.02 0.8
0.03 0.97 0 0.07 0.02 0.91
0.01 0.99 0 0.03 0.01 0.96
Equilibrium xA
20. S yn+1
PROBLEM (1) y1 max
To get maximum extract
concentration, it will be at
equilibrium with feed
concentration (x0).
y1max=0.27 B
xn x0 A
yA
Note
Here we make an approx. as
equilibrium not complete
(otherwise we have to work like
the next problem)
xA
21. S yn+1
y1=0.05
yn+1
M
b
PROBLEM (1)
As S/F=Vn+1/L0=10
a
Vn+1/(Vn+1+L0)=a/(a+b)
x0
10/11=a/(a+b)
a+b=10.1, a=9.18
B x0
xn A
Put Point(M). yA
xA
23. R
yn+1 y1
PROBLEM (1)
N.T.S=1.
B x0 A
yA xn
Equilibrium
Operating
xA
24. S yn+1
y1
y1
M
PROBLEM (1) b
As S/F=Vn+1/L0=10
a
V1/(V1+Ln)=a/(a+b)
xn
9/9.6=a/(a+b)
V1/(V1+Ln)=9/9.6
B x0
xn A
L0/(Vn+1+L0)=1/11……..* yA
V1+Ln= Vn+1+L0
V1 /(Vn+1+L0)=9/9.6……**
By dividing *&**
V1/ L0=(9*11)/(9.6*1)
V1/ L0=10.3125 lb/lb
xA
25. PROBLEM (2)
Givens:
A:Diphenyl hexane.
B:Decosane.
S:Furfural.
Feed contains 0.2 A & 0.8 B.
Multistage counter current system.
Solvent contains 0.005 A.
Raffinate product contains 0.01 A.
Required:
N.T.S if mass ratio of solvent to feed is 1.65.
Ratio of solvent to feed when N.T.S equals 3.
Maximum concentration of A that will be obtained.
26. PROBLEM (2)
Here the solubility saturation curve is given
between xS , xA &xB so, this means that the
solubility curve is closed.
xS xA xB
Also the equilibrium curve is given:
xA xB xS yA yB yS
Equilibrium
27. y
yn+1
b
PROBLEM (2) R
xn= 0.01
a
x0= 0.2
x0
yn+1 = 0.005
Vn+1/L0=1.65
Vn+1/(Vn+1+L0)=1.65/2.65=0 yn+1
x
S
.62
Vn+1/(Vn+1+L0)=a/(a+b) y1
0.62=a/9.5
a= 5.89 M
Put Point M
y1=0.15
N.T.S=4
xn X0=0.2
B A
28. y
PROBLEM (2)
To get S/F that makes
N.T.S=3.
We will assume y1. As
N.T.S decreases, y1 R
decreases too so;
yn+1 x
assume it less than y1
S
of N.T.S=4 y1 assumed
y1 assumed =0.1
M
What a luck!!
Vn+1/L0=1.8
xn x0 X0=0.2
B A
29. y
PROBLEM (2) R
To get y1max;
a) Assume y1max
b) From the equilibrium,
get x1 on the raffinate x
S yn+1
locus
y1 y 1max assumed
c) If the line connecting
y1max and x1 passes by M
xo, then the assumption
is true. If not, repeat the
steps
X1 X =0.2
xn 0
B A