Theory of dilute solution

 

Table Of Contents


  • <p> </p><p>Cover page i<br>Dedication ii<br>Acknowledgement iii<br>Tables of Content iv<br>Table of figures vi<br>

Chapter ONE

INTRODUCTION

  • <br>
  • 1.1Introduction 1<br>
  • 1.2History of colligative property 3<br>
  • 1.3Abnormal molecular mass 4</p><p>

Chapter TWO

LITERATURE REVIEW

  • Lowering of Vapour pressure<br>
  • 2.1Vapour pressure 5<br>
  • 2.2Raoult’s Law 8<br>
  • 2.3Ideal solutions and deviations from Raoult’s law 10<br>
  • 2.4Properties of real solutions 11<br>
  • 2.5Measurement of the lowering of vapour pressure 11<br>2.
  • 5.1The Barometric method 12<br>2.
  • 5.2The manometric method 12<br>2.
  • 5.3The Ostwald and Walker’s dynamic method 13</p><p>

Chapter THREE

SYSTEM DESIGN AND IMPLEMENTATION

  • The elevation of boiling point<br>
  • 3.1Introduction to boiling point elevation 15<br>
  • 3.2Relationship between the elevation of boiling point and lowering of vapour pressure 16<br>
  • 3.3The general equation for calculations at dilute concentration 18<br>
  • 3.4Ebullioscopic constants for some compounds 19<br>
  • 3.5Measurement of boiling point elevation 20<br>3.
  • 5.1The Landsberger-walker method 20<br>3.
  • 5.2The cottrell’s method 21<br>
  • 3.6Uses of boiling point elevation 23</p><p>

Chapter FOUR

SYSTEM TESTING AND EVALUATION

  • Freezing point depression<br>
  • 4.1Introduction to freezing point depression 24<br>
  • 4.2Relationship between depression of freezing point and lowering of vapour pressure 25<br>
  • 4.3Measurement of freezing point depression 26<br>4.
  • 3.1The Beckmann’s method 27<br>4.
  • 3.2The Rast’s camphor method 28<br>
  • 4.4Uses of freezing point depression 30<br>

Chapter FIVE

SUMMARY, CONCLUSION AND RECOMMENDATIONS

  • OSMOTIC PRESSURE<br>
  • 5.1Osmosis 32<br>
  • 5.2History of osmotic pressure 33<br>
  • 5.3What is osmotic pressure 33<br>
  • 5.4Applications of osmotic pressure 35<br>
  • 5.5Conclusion 37<br>References 38</p><p>TABLE OF FIGURES<br>Fig 1: Lowering of vapour pressure by a non-volatile solute.<br>Fig 2: Negative and positive deviation<br>Fig 3: Measurements of vapour pressure of aqueous solutions with a manometer<br>Fig 4: Ostwald-Walker method of measuring the relative lowering of vapour pressure<br>Fig 5: A graph of vapour pressure against temperature<br>Fig 6: Landberger-Walker method<br>Fig 7: Beckmann thermometer reading to 0.01K<br>Fig 8: Cottrell’s Apparatus<br>Fig 9: Relationship between lowering of vapour pressure and depression of freezing point<br>Fig 10: Relation between lowering of vapour pressure and depression of freezing point<br>Fig 11: Determination of depression of melting point by capillary method<br>Fig 12: Determination of depression of melting point by electrical method<br>Fig 13: The equilibrium involved in the calculation of osmotic pressure.<br>Fig 14: A simple version of the osmotic pressure experiment</p> <br><p></p>

Project Abstract

The theory of dilute solutions is a fundamental concept in physical chemistry that plays a crucial role in understanding the behavior of solutions at low solute concentrations. This theory provides a framework for analyzing the thermodynamic properties and interactions of solutes in a solvent when the solute concentration is significantly lower than that of the solvent. Key principles of the theory of dilute solutions include the ideal solution behavior, where the interactions between solute molecules and solvent molecules are considered to be negligible. This assumption simplifies the analysis of the system and allows for the application of various thermodynamic equations to describe the behavior of the solution. The concept of activity coefficients is central to the theory of dilute solutions, as it accounts for the deviation from ideal behavior that occurs at higher solute concentrations. Activity coefficients are used to correct the non-ideality of solutions and provide a more accurate representation of the thermodynamic properties of dilute solutions. Furthermore, the theory of dilute solutions is closely related to colligative properties, which are properties of solutions that depend on the number of solute particles rather than the specific nature of the solute. Colligative properties such as osmotic pressure, vapor pressure lowering, boiling point elevation, and freezing point depression are all influenced by the dilute nature of the solution and can be explained using the principles of the theory of dilute solutions. In addition to thermodynamic properties, the theory of dilute solutions also extends to the study of transport phenomena in solutions. The diffusion of solute molecules in a solvent, for example, is governed by the concentration gradient and is influenced by the interactions between solute and solvent molecules as described by the theory of dilute solutions. Overall, the theory of dilute solutions serves as a valuable tool for understanding the behavior of solutions at low solute concentrations and provides a theoretical foundation for studying a wide range of physical and chemical phenomena in solution chemistry. By considering the ideal behavior of solutes in a solvent and accounting for non-ideality using activity coefficients, this theory enhances our understanding of the thermodynamic and transport properties of dilute solutions.

Project Overview

<p> </p><p><strong>Introduction:</strong></p><p>The knowledge of the laws of solutions has been said, to be important because almost all the chemical processes which occur in nature, whether in animal or vegetable organisms, or in the non-living surface of the earth, and also those which are carried out in the laboratory, take place between substances in solution. For example, a sound judgment regarding physiological processes is impossible without this knowledge; and this holds true for the greater number of the scientifically and technically important reactions. Solutions are more important than gases, for the latter seldom react together at ordinary temperatures, whereas solutions present the best conditions for the occurrence of all chemical processes (Homer, 1980).</p><p>A dilute solution has a low concentration of the solute compared to the solvent. The opposite of a dilute solution is a concentrated solution, which has high levels of solute in the mixture.</p><p>Dilute solutions containing non-volatile solute exhibit the following properties:<br>(1) Lowering of the Vapour Pressure<br>(2) Elevation of the Boiling Point<br>(3) Depression of the Freezing Point<br>(4) Osmotic Pressure</p><p>The essential feature of these properties is that they depend only on the number of solute particles present in solution. Being closely related to each other through a common explanation, these have been grouped together under the class name Colligative Properties (Greek colligatus = Collected together) (Bahl, et al., 2012).</p><p>Physical properties can be divided into two categories. Extensive properties (such as mass and volume) depend on the size of the sample. Intensive properties (such as density and concentration) are characteristic properties of the substance; they do not depend on the size of the sample being studied. This section introduces a third category that is a subset of the intensive properties of a system. This third category, known as colligative properties, can only be applied to solutions. By definition, one of the properties of a solution is a colligative property if it depends only on the ratio of the number of particles of solute and solvent in the solution, not the identity of the solute.</p><p>A colligative property may be defined as one which depends on the number of particles in solution and not in any way on the size or chemical nature of the particles. In other words, colligative properties are a set of solution properties that can be reasonably approximated by assuming that the solution is ideal.<br>Here we consider only properties which result from the dissolution of nonvolatile solute in a volatile liquid solvent. They are essentially solvent properties which are changed by the presence of the solute. The solute particles displace some solvent molecules in the liquid phase and therefore reduce the concentration of solvent, so that the colligative properties are independent of the nature of the solute.<br>For a given solute-solvent mass ratio, all colligative properties are inversely proportional to solute molar mass.</p><p>Measurement of colligative properties for a dilute solution of a non-ionized solute such as urea or glucose in water or another solvent can lead to determinations of relative molar masses, both for small molecules and for polymers which cannot be studied by other means. Alternatively, measurements for ionized solutes can lead to an estimation of the percentage of dissociation taking place.<br>Colligative properties are mostly studied for dilute solutions, whose behavior may often be approximated as that of an ideal solution.</p> <br><p></p>

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