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In chemistry, colligative properties are properties of solutions that depend upon the ratio of the number of solute particles to the number of solvent molecules in a solution. Here we shall only consider those properties which result because of the dissolution of nonvolatile solute in a volatile liquid solvent. They are independent of the nature of the solute particles, and are due essentially to the dilution of the solvent by the solute. The word colligative is derived from the Latin colligatus meaning bound together, since these properties are bound together by the fact that they all depend on the number of solute particles and not on the type of chemical species present. This number can be related to the various units for concentration of solutions.
Colligative properties include:
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 accurate determinations of relative molar masses and of polymers too, which is often not possible. Alternatively, measurements for ionized solutes can lead to an estimation of the percentage of ionization taking place.
Colligative properties are mostly studied for dilute solutions, whose behavior may often be approximated as that of an ideal solution.
The vapor pressure of a liquid is the pressure of a vapor in equilibrium with the liquid phase. The vapor pressure of a solvent is lowered by addition of a non-volatile solute to form a solution.
is the vapor pressure of the pure component i (= A, B, ...) and is the mole fraction of the component i in the solution
For a solution with a solvent (A) and one non-volatile solute (B), and
The vapor pressure lowering relative to pure solvent is , which is proportional to the mole fraction of solute.
If the solute dissociates in solution, then the vapor pressure lowering is increased by the van't Hoff factor , which represents the true number of solute particles for each formula unit. For example, the strong electrolyte MgCl2 dissociates into one Mg2+ ion and two Cl- ions, so that if ionization is complete, i = 3 and . The measured colligative properties show that i is somewhat less than 3 due to ion association.
Addition of solute to form a solution stabilizes the solvent in the liquid phase, and lowers the solvent chemical potential so that solvent molecules have less tendency to move to the gas or solid phases. As a result, liquid solutions slightly above the solvent boiling point at a given pressure become stable, which means that the boiling point increases. Similarly, liquid solutions slightly below the solvent freezing point become stable meaning that the freezing point decreases. Both the boiling point elevation and the freezing point depression are proportional to the lowering of vapor pressure in a dilute solution.
These properties are colligative in systems where the solute is essentially confined to the liquid phase. Boiling point elevation (like vapor pressure lowering) is colligative for non-volatile solutes where the solute presence in the gas phase is negligible. Freezing point depression is colligative for most solutes since very few solutes dissolve appreciably in solid solvents.
The boiling point of a pure solvent is increased by the addition of a non-volatile solute, and the elevation can be measured by ebullioscopy. It is found that
The boiling point is the temperature at which there is equilibrium between liquid and gas phases. At the boiling point, the number of gas molecules condensing to liquid equals the number of liquid molecules evaporating to gas. Adding a solute dilutes the concentration of the liquid molecules and reduces the rate of evaporation. To compensate for this and re-attain equilibrium, the boiling point occurs at a higher temperature.
If the solution is assumed to be an ideal solution, Kb can be evaluated from the thermodynamic condition for liquid-vapor equilibrium. At the boiling point the chemical potential μA of the solvent in the solution phase equals the chemical potential in the pure vapor phase above the solution.
The freezing point () of a pure solvent is lowered by the addition of a solute which is insoluble in the solid solvent, and the measurement of this difference is called cryoscopy. It is found that
Here Kf is the cryoscopic constant, equal to 1.86°C kg/mol for the freezing point of water. Again "i" is the van't Hoff factor and m the molality.
In the liquid solution, the solvent is diluted by the addition of a solute, so that fewer molecules are available to freeze. Re-establishment of equilibrium is achieved at a lower temperature at which the rate of freezing becomes equal to the rate of liquefying. At the lower freezing point, the vapor pressure of the liquid is equal to the vapor pressure of the corresponding solid, and the chemical potentials of the two phases are equal as well. The equality of chemical potentials permits the evaluation of the cryoscopic constant as , where ΔHfus is the solvent molar enthalpy of fusion.
The osmotic pressure of a solution is the difference in pressure between the solution and the pure liquid solvent when the two are in equilibrium across a semipermeable membrane, which allows the passage of solvent molecules but not of solute particles. If the two phases are at the same initial pressure, there is a net transfer of solvent across the membrane into the solution known as osmosis. The process stops and equilibrium is attained when the pressure difference equals the osmotic pressure.
These are analogous to Boyle's law and Charles's Law for gases. Similarly, the combined ideal gas law, , has as analog for ideal solutions , where is osmotic pressure; V is the volume; n is the number of moles of solute; R is the molar gas constant 8.314 J K−1 mol−1; T is absolute temperature; and i is the Van 't Hoff factor.
The osmotic pressure is then proportional to the molar concentration , since
The osmotic pressure is proportional to the concentration of solute particles ci and is therefore a colligative property.
As with the other colligative properties, this equation is a consequence of the equality of solvent chemical potentials of the two phases in equilibrium. In this case the phases are the pure solvent at pressure P and the solution at total pressure P + π.