CHEMICAL ENGINEERING

Similar documents
If two volatile and miscible liquids are combined to form a solution, Raoult s law is not obeyed. Use the experimental data in Table 9.

modeling of equilibrium and dynamic multi-component adsorption in a two-layered fixed bed for purification of hydrogen from methane reforming products

Assignment 4. Adsorption Isotherms

Thermodynamics General

Energy, Entropy, and Availability Balances Phase Equilibria. Nonideal Thermodynamic Property Models. Selecting an Appropriate Model

Diffusion Mass Transfer

Mass transfer in multi-component mixtures

Lecture 17. Membrane Separations [Ch. 14]

Adsorption: A gas or gases from a mixture of gases or a liquid (or liquids) from a mixture of liquids is bound physically to the surface of a solid.

Mass Transfer Processes

Name: SID: Discussion Session:

Chapter 3 Thermochemistry of Fuel Air Mixtures

Introduction to Vapor/Liquid Equilibrium, part 2. Raoult s Law:

CHEMICAL REACTIONS AND DIFFUSION

Supplementary Notes for Chapter 9 Mixture Thermodynamics

Module 1 : The equation of continuity. Lecture 1: Equation of Continuity

Open Systems: Chemical Potential and Partial Molar Quantities Chemical Potential

CHE-201. I n t r o d u c t i o n t o Chemical E n g i n e e r i n g. C h a p t e r 6. Multiphase Systems

Week3, Chapter 4. Position and Displacement. Motion in Two Dimensions. Instantaneous Velocity. Average Velocity

4.2 Chemical Driving Force

LNG CARGO TRANSFER CALCULATION METHODS AND ROUNDING-OFFS

Chapter 18, Part 1. Fundamentals of Atmospheric Modeling

10.34 Numerical Methods Applied to Chemical Engineering Fall Homework #3: Systems of Nonlinear Equations and Optimization

Lecture 12. Transport in Membranes (2)

( ) 1/ 2. ( P SO2 )( P O2 ) 1/ 2.

Solution Thermodynamics

Number Average Molar Mass. Mass Average Molar Mass. Z-Average Molar Mass

Solution Thermodynamics

Prediction of Ultrasonic Velocity in Binary Mixtures of a Nuclear Extractant and Monocarboxylic Acids using Several Theoretical Models

Thermodynamics II. Department of Chemical Engineering. Prof. Kim, Jong Hak

KINETICS OF GAS HYDRATE FORMATION FROM PYROLYSIS GAS IN WATER-IN-OIL EMULSION SYSTEM

Influence Of Operating Conditions To The Effectiveness Of Extractive Distillation Columns

NAME and Section No. it is found that 0.6 mol of O

General Thermodynamics for Process Simulation. Dr. Jungho Cho, Professor Department of Chemical Engineering Dong Yang University

Chemical Equilibrium. Chapter 6 Spontaneity of Reactive Mixtures (gases) Taking into account there are many types of work that a sysem can perform

Estimation of the composition of the liquid and vapor streams exiting a flash unit with a supercritical component

Lecture. Polymer Thermodynamics 0331 L Chemical Potential

PETE 310 Lectures # 24 & 25 Chapter 12 Gas Liquid Equilibrium

I wish to publish my paper on The International Journal of Thermophysics. A Practical Method to Calculate Partial Properties from Equation of State

Principles of Food and Bioprocess Engineering (FS 231) Solutions to Example Problems on Heat Transfer

McCabe-Thiele Diagrams for Binary Distillation

Exercises of Fundamentals of Chemical Processes

VAPOR LIQUID EQUILIBRIUM DATA GENERATION FOR ACETIC ACID AND p-xylene AT ATMOSPHERIC PRESSURE

Gasometric Determination of NaHCO 3 in a Mixture

A Modulated Hydrothermal (MHT) Approach for the Facile. Synthesis of UiO-66-Type MOFs

ChE 512: Topic 1 Reactions at a fluid non-porous solid interface. P.A. Ramachandran

#64. ΔS for Isothermal Mixing of Ideal Gases

Wilbur and Ague 4 WILBUR AND AGUE; APPENDIX DR1. Two-dimensional chemical maps as well as chemical profiles were done at 15 kv using

Vapor-Liquid Equilibria for Water+Hydrochloric Acid+Magnesium Chloride and Water+Hydrochloric Acid+Calcium Chloride Systems at Atmospheric Pressure

CinChE Problem-Solving Strategy Chapter 4 Development of a Mathematical Model. formulation. procedure

Process Modeling. Improving or understanding chemical process operation is a major objective for developing a dynamic process model

Three-Phase Distillation in Packed Towers: Short-Cut Modelling and Parameter Tuning

Design Equations. ν ij r i V R. ν ij r i. Q n components. = Q f c jf Qc j + Continuous Stirred Tank Reactor (steady-state and constant phase)

Basic concept of reactive flows. Basic concept of reactive flows Combustion Mixing and reaction in high viscous fluid Application of Chaos

Application of Activity Coefficient Models in VLE Determination for Azeotropic System Using Othmer Type Ebulliometer

The ChemSep Book. Harry A. Kooijman Consultant. Ross Taylor Clarkson University, Potsdam, New York University of Twente, Enschede, The Netherlands

PART I: MULTIPLE CHOICE (32 questions, each multiple choice question has a 2-point value, 64 points total).

Electrical double layer: revisit based on boundary conditions

INTRODUCTION TO CHEMICAL PROCESS SIMULATORS

...Thermodynamics. If Clausius Clapeyron fails. l T (v 2 v 1 ) = 0/0 Second order phase transition ( S, v = 0)

MASS TRANSFER Lesson 1 BY DR. ARI SEPPÄLÄ AALTO UNIVERSITY

The influence of non-ideal vapor-liquid-equilibrium on vaporization of multicomponent hydrocarbon fuels

Chemical Engineering Department University of Washington

y i x P vap 10 A T SOLUTION TO HOMEWORK #7 #Problem

Solutions to Exercises in Astrophysical Gas Dynamics

Airflow and Contaminant Simulation with CONTAM

Chapter One Mixture of Ideal Gases

Investigation of High-Pressure Phase Equilibrium with the Observation of the Cloud Point

Electrochemical Equilibrium Electromotive Force

Lecture 11. Transport in Membranes (1)

3) Thermodynamic equation to characterize interfaces

Robert Eisberg Second edition CH 09 Multielectron atoms ground states and x-ray excitations

Week 9 Chapter 10 Section 1-5

Module 3 LOSSY IMAGE COMPRESSION SYSTEMS. Version 2 ECE IIT, Kharagpur

Name ID # For relatively dilute aqueous solutions the molality and molarity are approximately equal.

Lecture 5.8 Flux Vector Splitting

University of Washington Department of Chemistry Chemistry 452/456 Summer Quarter 2014

Chapter 11 Structure of Matter 133 Answers to the Conceptual Questions

Be true to your work, your word, and your friend.

Thermodynamics Second Law Entropy

Problem Set #6 solution, Chem 340, Fall 2013 Due Friday, Oct 11, 2013 Please show all work for credit

University Physics AI No. 10 The First Law of Thermodynamics

CHAPTER 3 MODELLING OF DISTILLATION COLUMN

Adiabatic Sorption of Ammonia-Water System and Depicting in p-t-x Diagram

Ionization fronts in HII regions

Solid state reactions. Often defined as reactions between two solids. Here the definition is extended to any reaction involving a solid:

Module 1 : The equation of continuity. Lecture 5: Conservation of Mass for each species. & Fick s Law

Spin-rotation coupling of the angularly accelerated rigid body

Appendix II Summary of Important Equations

Dynamic Model of Dividing Wall Column for Separation of Ternary System

Substance and heat transfer in multistage systems

MATH 5630: Discrete Time-Space Model Hung Phan, UMass Lowell March 1, 2018

(1) The saturation vapor pressure as a function of temperature, often given by the Antoine equation:

ELASTIC WAVE PROPAGATION IN A CONTINUOUS MEDIUM

Modeling of CO 2 Cut in CBM Production

University of Washington Department of Chemistry Chemistry 452/456 Summer Quarter 2014

V T for n & P = constant

Pulse Coded Modulation

A New Steps Sequence Table to Improve the Performance of the Jam Petrochemical H 2 -PSA Industrial Plant

1. Mathematical models of the chromatographic process

Transcription:

Postal Correspondence GATE & PSUs -MT To Buy Postal Correspondence Packages call at 0-9990657855 1

TABLE OF CONTENT S. No. Ttle Page no. 1. Introducton 3 2. Dffuson 10 3. Dryng and Humdfcaton 24 4. Absorpton and Strppng 34 5. Dstllaton 40 6. Extracton and Leachng 57 7. Adsorpton 64 Annexure - A Important Formulae used n Mass Transfer 66 Annexure - B Practce Set 72 Annexure - C Gate Based Questons 86 2

Chapter-1 Introducton The process of mass transfer occurs due to concentraton dfference of mxture components. It occurs from a regon of hgher concentraton to a regon of lower concentraton. Concentraton dfference s the pllar of mass transfer. Varous separaton technques such as dstllaton, gas adsorpton, lqud extracton, dryng, crystallzaton, etc. are studed n Mass transfer, where operaton may occur sothermally or non-sothermally. Mass transfer operaton may occur smultaneously wth heat transfer, for example; Dryng, Humdfcaton, Dstllaton, crystallzaton etc. Mass transfer operaton may occur n one drecton example, gas absorpton. The contactng can be done n sx ways namely, Gas-Gas, GasLqud, Gas-sold, Lqud-Lqud and Lqud-Sold and Sold-Sold. (a) Lqud-Vapour Dstllaton. (b) Lqud-gas Gas absorpton, strppng, Humdfcaton and Dehumdfcaton. (c) Lqud-Sold Crystallzaton, Leachng, Adsorpton. (d) Lqud- Lqud Extracton. (e) Sold-Gas Adsorpton, Dryng. The equllbrum between phases s attaned after suffcently long tme. Snce Mass transfer occurs due to both molecular dffuson and turbulence, the detaled study of factors affectng mass transfer s studed. At the phase nterface there s no resstance due to thermodynamc equllbrum (T, P, ) at nterface. Rate of mass transfer s measured by devaton from equllbrum.e. hgher the devaton, hgher s the drvng force. 1.1. Some Important Defntons: 1) Dstllaton: Dstllaton s a vapour-lqud operaton n whch the mxture components are separated by use of thermal energy. When lqud mxture s heated, dfferent components exert dfferent vapour pressure, expressed n terms of relatve volatlty. Ths pressure dfference results n separaton of components n such a way that the top product contans hgher amount of lght component and bottom products contans hgher amounts of heaver component, as shown n fgure 1.1. A dstllaton example s separaton of crude petroleum nto gasolne, kerosene, etc. Fg. 1.1. Schematc dagram of a dstllaton column 3

2) Absorpton and Strppng: Gas absorpton s a gas-lqud operaton n whch one or more consttuents of a gas mxture are separated by usng a sutable lqud solvent.e. component moves from gas phase to lqud phase as shown n fgure 1.2. Example of gas absorpton methods s ammona washng from ammona-ar mxture by means of water. Strppng s opposte of absorpton.e. a component moves from lqud phase to gas phase. 3) Fg. 1.3. Schematc dagram of a Lqud-Lqud Extractor Crystallzaton: It s lqud-sold operaton n whch we obtan unform crystals of good purty. The saturated lqud s subjected to changes n temperature and pressure n such a way that crystals get separated from the feed lquor as shown n the fgure 1.4. 5) Fg. 1.2. Schematc dagram of an absorpton column Lqud-Lqud Extracton: It s a lqud-lqud operaton, also called as solvent extracton, n whch components of a lqud mxture are separated by treatng t wth sutable solvent whch dssolves one or more consttuents of mxture more preferably. It s an effcent separaton process n cases where separaton s ether not possble or not economcal by usng dstllaton eg. Separaton of components of an azeotropc mxture. 4) Fg. 1.4. Schematc dagram of a crystallzer Dryng: Dryng s gas-sold operaton n whch a relatvely small amount of water s removed from sold materal, by contactng t wth a contnuous stream of gas (ar) as shown n fgure 1.5. Fg. 1.5. Schematc dagram of a dryer 1.2. Important concepts to remember: 1) Ideal gas law : PV nrt Where, P Pressure (kpa), V Volume (m3) 4

n number of moles (kmol), T Temperature (K) m2 kpa R 8.31451 Unversal gas constant kmol K v or psa ) and partal pressure (p A, pb ) : The vapour pressure of a lqud 2) Vapour Pressure (p A s defned as the absolute pressure at whch the lqud and ts vapour are n equllbrum at gven temperature n a closed vessel. The partal pressure of a gas component that s present n a gaseous mxture, s a pressure that would be exerted by that component f t alone were present n the same volume and at the same temperature. p A x A p Av 3) Dalton s law : Dalton s law mathematcally s gven by: P pa + p B, Where P s the total pressure exerted by gaseous mxture. pa and pb are the partal pressures of component gases A and B respectvely. 4) More Volatle Component: More volatle component s lower bolng pont component or the component wth hgher vapour pressure at a gven temperature. It s also called as the lghter component. 5) Less Volatle Component: In a bnary system, t s the component wth hgher bolng pont or lower vapour pressure at a gven temperature. It s also called as the heaver component. 6) Concentraton: 6.1. Mass Concentraton (Also known as mascon): It s defned as the mass of consttuent dvded by the volume of mxture. It s denoted by or. m where, m mass of consttuent, V volume of mxture. V For a pure chemcal the mass concentraton equals ts densty. For Bnary system havng components A and B, mass densty ( ρ ) of soluton s gven byρ A + ρ B ρ, where ρ A and ρ B are mass concentraton s of A and B respectvely. 6.2. Molar concentraton (Molarty): Molar concentraton s defned as the number of moles of speces A per unt volume of the soluton. 3 Mathematcally, It s gven as c A (kmol/m ) na ρ A V MA where, n A moles of speces A, MA molecular weght of component A For a bnary system of A and B, the total molar concentraton of the soluton s gven by C ca +cb 6.3. Mass Fracton (x A') : 5

WA, where WA and WB are gven weghts of A and B respectvely x A' WA + WB 6.4. Mole Fracton (x A ) : The mole fracton (xa) of speces A can be defned as the rato of number of moles of component to the total no. of moles. Mathematcally, for a bnary system, x A na na + nb Note: x A + x B 1 and x' A + x' B 1 In gas phase the concentratons are expressed n terms of partal pressures. In case of an deal gas p A V n A RT or ca na pa V RT Where, p A partal pressure of speces A n the mxture n A number of moles of A V molar volume of mxture T absolute temperature (K) R unversal gas constant xa n terms of p A s gven as: xa ca pa /RT pa C P/RT P Where P s the total pressure exerted by the gas mxture. C ca + cb pa pb P + RT RT RT 7) Velocty of Speces: Dfferent chemcal speces are movng at dfferent velocty n a dffusng mxture. The bulk velocty of the mxture would be some sort of an average velocty. For a mxture of n speces local mass average velocty u s defned as n ρ u u 1 n ρ Where u s velocty of th speces. 1 In case of bnary system, u ρ A u A +ρ B u B ρ n c U Local molar average velocty U of mxture s gven by U 1n c 1 6

c U +c U In a bnary system, U A A B B C 8) Flux: Flux s a vector quantty. The amount of speces (mass or molar unts) that crosses a unt area per unt tme s called flux (mass transfer flux or molar flux respectvely) of a speces. 8.1. Mass Flux: The mass flux of speces s defned as the mass of speces that passes through a unt area per unt tme. It s also defned as mass flow rate per unt area. () Mass flux relatve to fxed coordnate s gven by, ρ u For a bnary system, the mass flux of A and B relatve to statonary coordnate are A A u A and B ρ Bu B respectvely () Mass flux relatve to the mass average velocty u s gven by, j (u u ) For a bnary system, the mass flux of A and B relatve to mass average velocty are- ja ρ A (u A u) and jb ρ B(u B u) respectvely 8.2. Molar Flux: Molar flux s defned as moles of speces that passes through a unt area per unt tme. It s also defned as molar flow rate per unt area. () Molar flux relatve to the statonary coordnate s gven by, N c U For a bnary system, the molar fluxes of A and B wth respect to statonary coordnates are- N A ca U A and N B c c BU B respectvely () Molar flux relatve to molar average velocty U (also known as bulk velocty) s gven by, J c (U U) For a bnary system, the molar fluxes of A and B wth respect to an observer movng wth bulk velocty, J A c A (U A U) and J B c B (U B U) respectvely 1.3. Dmensonless numbers used n mass transfer: (1) Sherwood number (Sh) k'l convectve mass transport Sh, k' Mass transfer coeffcent DAB molecular mass transport Where L s the characterstcs length (2) Schmdt Number (Sc) Sc 1 Momentum dffusvty ν D AB DAB Mass dffusvty (3) Prandtl Number (Pr) 7

Pr C p Momentum dffusvty α K Thermal dffusvty (4) Lews Number (Le) Le K 1 Momentum dffusvty α Sc Mass dffusvty Pr DAB ρcp DAB (5) Reynolds Number (Re) ρvd Inertal force Re μ Vscous force (6) Stanton number (St) k' Sh St υ ReSc (7) Peclet number (Pe) Pe ReSc 1. Calculate the equllbrum composton of the lqud and vapour phase for a mxture of methyl alcohol and water at a temperature of 400 K and under a pressure of 45 kpa. Assume that both lqud and vapour behave deally Data : Vapour pressure of water at 400 K 15 kpa Vapour pressure of methanol at 400 K 60 kpa Soluton: Let x1 and y1 be mole fracton of methyl alcohol n lqud and vapour respectvely. p1 partal pressure of methyl alcohol p1 p1v x1 60x1 p2 water partal pressure p2 p2v x 2 15 1 x1 and we know total pressure P p1 p2 45 60x1 +15(1 x1) 45 15 60x1 15x1 30 45x1 x1 0.67 y1 p1 p1x1 60 0.67 0.89 P P 45 Hence at equllbrum: Lqud phase 0.67 mole fracton of methyl alcohol 8

Vapour phase 0.89 mole fracton of methyl alcohol. 2. A mxture of benzene and toluene bols at 380 K under a pressure of 101.325 kpa. Determne the composton of bolng lqud assumng that mxture obeys Raoult s law. At 380 K the vapour pressure of benzene s 160 kpa and the toluene s 70 kpa. Soluton: Let mole fracton of benzene n lqud xa P 100.325 kpa (gven data) pa 160 kpa p B 70 kpa xa P p vb p va p vb xa 101.325 70 0.348 0.348 160 70 Mole fracton of benzene n bolng lqud 0.348 100 34.8 Hence composton of the bolng lqud 34.8 mole% 9

10