This document discusses extraction processes and equipment design. It defines extraction as removing one or more solutes from a liquid by transferring them into a second, immiscible liquid phase called the solvent. There are three main types of extraction processes: co-current contact with immiscible solvents, countercurrent contact with immiscible solvents, and continuous extraction in columns using countercurrent contact with partially miscible solvents. The document provides steps for calculating the number of theoretical stages needed for extraction column design based on equilibrium data between solute compositions in the raffinate and extract streams. It also gives an example problem demonstrating how to design an extraction process and determine the equilibrium stage number.
This document discusses extraction processes and equipment design. It defines extraction as removing one or more solutes from a liquid by transferring them into a second, immiscible liquid phase called the solvent. There are three main types of extraction processes: co-current contact with immiscible solvents, countercurrent contact with immiscible solvents, and continuous extraction in columns using countercurrent contact with partially miscible solvents. The document provides steps for calculating the number of theoretical stages needed for extraction column design based on equilibrium data between solute compositions in the raffinate and extract streams. It also gives an example problem demonstrating how to design an extraction process and determine the equilibrium stage number.
This document discusses extraction processes and equipment design. It defines extraction as removing one or more solutes from a liquid by transferring them into a second, immiscible liquid phase called the solvent. There are three main types of extraction processes: co-current contact with immiscible solvents, countercurrent contact with immiscible solvents, and continuous extraction in columns using countercurrent contact with partially miscible solvents. The document provides steps for calculating the number of theoretical stages needed for extraction column design based on equilibrium data between solute compositions in the raffinate and extract streams. It also gives an example problem demonstrating how to design an extraction process and determine the equilibrium stage number.
UNIVERSITY OF BASRAH COLLEGE OF ENGINEERING This chapter includes the following items 1- Extraction definition types
2- Extraction types
3- Extractor design (calculation the stage number)
Co-current contact with immiscible solvents
Countercurrent contact with immiscible solvents Continuous extraction in columns Countercurrent contact with partially miscible solvents 1-Introduction : Extraction Processes and Equipment Extraction is a process where one or more solutes are removed from a liquid by transferring the solute(s) into a second liquid phase. The second liquid phase, the solvent, is a mass separating agent that must be recovered later. The two liquid phases must be immiscible (that is, insoluble in each other) or partially immiscible. 3-Extractor design (calculation the stage number) Co-current contact with immiscible solvents 1-2 : Modes of Extraction Countercurrent contact with immiscible solvents Steps solution to find stage number for desiging the process:
Draw equilibrium data between composition
of solute in raffinate (X) and its composition in extract (Y) Select the point XF on x-axis . Draw an operating line, of slope (A/S), which passes through the points (Xf , Y1) and (Xn, Yn+1) draw steps between the operating line and the equilibrium curve where it was noted the operating line connects the compositions of the raffinate stream leaving and the fresh solvent stream entering a unit, Xn and Yn+1 Continuous extraction in columns: Find the length (Z) from equation below:
find LR or KR
In a similar manner, for extraction based on extract phase
The relation between HOR (based on extract and based on raffinate
HOE) Example : Packed column is used to extract acetic acid from an aqueous solution using benzene solvent. It has height 1.4 m cross-sectional area of 0.0045 m2, what is the overall transfer coefficient and the height of the transfer unit required for designing the column. 5- Countercurrent contact with partially miscible solvents 5-1Selection the composition of the raffinate and extract to the extraction process below 5-2 Design and find the equilibrium stage in Countercurrent unit Example • A 50 % solution of solute C in solvent A is extracted with a second solvent B in a countercurrent multiple contact extraction unit. • The mass of B is 25 %, • the final raffinate contains 15 % of solute C. Solution: Select F, representing the feed, on AC at C = 0.50, A = 0.50. B is the solvent, draw FB is joined and M located such that Mass B/ Mass A = FM/MB = 0.25. Select final raffinate (Rn) is located on the equilibrium curve ( C = 0.15, B = 0.01, A = 0.84) 5-4 Minimum and Maximum Solvent-to-Feed Flow-Rate Ratios Example Solution Effective solvent