World Library  
Flag as Inappropriate
Email this Article

Raoult's law

Article Id: WHEBN0000038873
Reproduction Date:

Title: Raoult's law  
Author: World Heritage Encyclopedia
Language: English
Subject: Distillation, Azeotrope, Spinning band distillation, Bancroft point, Dalton's law
Publisher: World Heritage Encyclopedia

Raoult's law

Raoult's law is a law of thermodynamics established by French physicist François-Marie Raoult in 1882.[1] It states that the partial vapor pressure of each component of an ideal mixture of liquids is equal to the vapor pressure of the pure component multiplied by its mole fraction in the mixture.

Mathematically, Raoult's law for a single component in an ideal solution is stated as

p_i = p^{\star}_i x_i,

where p_i is the partial vapor pressure of the component i in the gaseous mixture (above the solution), p_i^{\star} is the vapor pressure of the pure component i, and x_i is the mole fraction of the component i in the mixture (in the solution).[2]

Once the components in the solution have reached equilibrium, the total vapor pressure of the solution can be determined by combining Raoult's law with Dalton's law of partial pressures to give

p = p^{\star}_{\rm A} x_{\rm A} + p^{\star}_{\rm B} x_{\rm B} + \cdots.

If a non-volatile solute (zero vapor pressure, does not evaporate) is dissolved into a solvent to form an ideal solution, the vapor pressure of the final solution will be lower than that of the pure solvent.


Vapor pressure of a binary solution that obeys Raoult's law. The black line shows the total vapor pressure as a function of the mole fraction of component B, and the two green lines are the partial pressures of the two components.

Raoult's law is a phenomenological law that assumes ideal behavior based on the simple microscopic assumption that intermolecular forces between unlike molecules are equal to those between similar molecules: the conditions of an ideal solution. This is analogous to the ideal gas law, which is a limiting law valid when the interactive forces between molecules approach zero, for example as the concentration approaches zero. Raoult's law is instead valid if the physical properties of the components are identical. The more similar the components are, the more their behavior approaches that described by Raoult's law. For example, if the two components differ only in isotopic content, then Raoult's law is essentially exact.

Comparing measured vapor pressures to predicted values from Raoult's law provides information about the true relative strength of intermolecular forces. If the vapor pressure is less than predicted (a negative deviation), fewer molecules of each component than expected have left the solution in the presence of the other component, indicating that the forces between unlike molecules are stronger. The converse is true for positive deviations.

For a solution of two liquids, A and B, Raoult's law predicts that if no other gases are present, then the total vapor pressure p above the solution is equal to the weighted sum of the "pure" vapor pressures of the two components, p_A and p_B. Thus the total pressure above the solution of A and B would be

p = p^{\star}_{\rm A} x_{\rm A} + p^{\star}_{\rm B} x_{\rm B}.

Since the sum of the mole fractions is equal to one,

p = p^{\star}_{\rm A} (1-x_{\rm B}) + p^{\star}_{\rm B} x_{\rm B} = p^{\star}_{\rm A} + (p^{\star}_{\rm B}-p^{\star}_{\rm A}) x_{\rm B}.

This is a linear function of the mole fraction x_B, as shown in the graph.

Thermodynamic considerations

Raoult's law was originally discovered as an idealised experimental law. Using Raoult's law as the definition of an ideal solution, it is possible to deduce that the chemical potential of each component of the liquid is given by

\mu _i = \mu_i^{\star} + RT\ln x_i\,,

where \mu_i^{\star} is the chemical potential of component i in the pure state. This equation for the chemical potential may then be used to derive other thermodynamic properties of an ideal solution. (see Ideal solution)

However, a more fundamental thermodynamic definition of an ideal solution is one in which the chemical potential of each component is given by the above formula. Assuming also that the vapor mixture acts as an ideal gas, it is then possible to re-derive Raoult's law as follows.

If the system is at equilibrium, then the chemical potential of the component i must be the same in the liquid solution and in the vapor above it. That is,

\mu _{i,{\rm liq}} = \mu _{i,{\rm vap}}.\,

Assuming the liquid is an ideal solution, and using the formula for the chemical potential of a gas, gives:

\mu _{i,{\rm liq}}^{\star} + RT\ln x_i = \mu_{i,{\rm vap}}^\ominus + RT\ln \frac

where f_i is the fugacity of the vapor of i and ^\ominus indicates the reference state.

The corresponding equation for pure i in equilibrium with its (pure) vapor is:

\mu _{i,{\rm liq}}^{\star} = \mu _{i,{\rm vap}}^\ominus + RT\ln \frac}

where * indicates the pure component.

Subtracting the equations gives us

RT\ln x_i = RT\ln \frac

which re-arranges to

f_i = x_i f_i^{\star}.

The fugacities can be replaced by simple pressures if the vapor of the solution behaves ideally i.e.

p_i = x_i p_i^{\star}

which is Raoult's Law.

Ideal mixing

An ideal solution would follow Raoult's Law, but ideal solutions do not exist. The fact that the vapor above the liquid is taken to be ideal is the least of our worries. Interactions between gas molecules are typically quite small, especially if the vapor pressures are low. The interactions in a liquid however are very strong. For a solution to be ideal we must assume that it does not matter whether a molecule A has another A as neighbor or a B molecule. This is approximately true only if the two species are almost identical chemically. One can see that from considering the Gibbs free energy change of mixing:

\Delta_{\rm mix} G = nRT(x_1\ln x_1 + x_2\ln x_2).\,

This is always negative, so mixing is spontaneous. However the expression is, apart from a factor –T, equal to the entropy of mixing. This leaves no room at all for an enthalpy effect and implies that \Delta_{\rm mix} H must be equal to zero and this can only be true if the interactions U between the molecules are indifferent.

It can be shown using the Gibbs–Duhem equation that if Raoult's law holds over the entire concentration range x = 0–1 in a binary solution then, for the second component, the same must also hold.

If deviations from the ideal are not too large, Raoult's law is still valid in a narrow concentration range when approaching x = 1 for the majority phase (the solvent). The solute also shows a linear limiting law, but with a different coefficient. This law is known as Henry's law.

The presence of these limited linear regimes has been experimentally verified in a great number of cases. In a perfectly ideal system, where ideal liquid and ideal vapor are assumed, a very useful equation emerges if Raoult's law is combined with Dalton's Law.

x_i = \frac{y_i p_{\rm total}}{p_{i,{\rm eqm}}}\,,

where x_i is the mole fraction of component i in the solution and y_i is its mole fraction in the gas phase. This equation shows that, for an ideal solution where each pure component has a different vapor pressure, the gas phase is enriched in the component with the higher pure vapor pressure and the solution is enriched in the component with the lower pure vapor pressure. This phenomenon is the basis for distillation.

Non-ideal mixing

Raoult's Law may be adapted to non-ideal solutions by incorporating two factors that account for the interactions between molecules of different substances. The first factor is a correction for gas non-ideality, or deviations from the ideal-gas law. It is called the fugacity coefficient (\phi_{p,i}). The second, the activity coefficient (\gamma_i), is a correction for interactions in the liquid phase between the different molecules.

This modified or extended Raoult's law is then written:

p_{i} \phi_{p,i} = p_i^{\star} \gamma_i x_i.\,

Real solutions

Many pairs of liquids are present in which there is no uniformity of attractive forces, i.e., the adhesive and cohesive forces of attraction are not uniform between the two liquids, so that they deviate from the Raoult's law applied only to ideal solutions.

Negative deviation

Positive and negative deviations from Raoult's law. Maxima and minima in the curves (if present) correspond to azeotropes or constant boiling mixtures.
If the vapor pressure of a mixture is lower than expected from Raoult's law, there is said to be a negative deviation. This is evidence that the adhesive forces between different components are stronger than the average cohesive forces between like components. In consequence each component is retained in the liquid phase by attractive forces that are stronger than in the pure liquid so that its partial vapor pressure is lower.

For example, the system of chloroform (CHCl3) and acetone (CH3COCH3) has a negative deviation[3] from Raoult's law, indicating an attractive interaction between the two components that has been described as a hydrogen bond.[4] The system hydrochloric acid - water has a large enough negative deviation to form a minimum in the vapor pressure curve known as a (negative) azeotrope, corresponding to a mixture that evaporates without change of composition.[5]

Positive deviation

When the cohesive forces between like molecules are greater than the adhesive forces, the dissimilarities of polarity leads both components to escape solution more easily. Therefore, the vapor pressure is greater than expected from the Raoult's law, showing positive deviation. If the deviation is large, then the vapor pressure curve shows a maximum at a particular composition and form a positive azeotrope. Some mixtures in which this happens are (1) benzene and methanol, (2) carbon disulfide and acetone, and (3) chloroform and ethanol.

Electrolytes solutions

The expression of the law for this case includes the van 't Hoff factor.

See also


Chapter 24, D A McQuarrie, J D Simon Physical Chemistry: A Molecular Approach. University Science Books. (1997)

E. B. Smith Basic Chemical Thermodynamics. Clarendon Press. Oxford (1993)

  1. ^ Barnett, Martin K. (2001), A Dictionary of the History of Science, Informa Health Care, p. 287 . Extract.
  2. ^ A to Z of Thermodynamics by Pierre Perrot. ISBN 0-19-856556-9
  3. ^ P. Atkins and J. de Paula, Physical Chemistry (8th ed., W.H. Freeman 2006) p.146
  4. ^ K. Kwak, D.E. Rosenfeld, J.K. Chung and M.D. Fayer, J. Phys. Chem. B (2008), 112, 13906–13915
  5. ^ Atkins and de Paula, p.184
This article was sourced from Creative Commons Attribution-ShareAlike License; additional terms may apply. World Heritage Encyclopedia content is assembled from numerous content providers, Open Access Publishing, and in compliance with The Fair Access to Science and Technology Research Act (FASTR), Wikimedia Foundation, Inc., Public Library of Science, The Encyclopedia of Life, Open Book Publishers (OBP), PubMed, U.S. National Library of Medicine, National Center for Biotechnology Information, U.S. National Library of Medicine, National Institutes of Health (NIH), U.S. Department of Health & Human Services, and, which sources content from all federal, state, local, tribal, and territorial government publication portals (.gov, .mil, .edu). Funding for and content contributors is made possible from the U.S. Congress, E-Government Act of 2002.
Crowd sourced content that is contributed to World Heritage Encyclopedia is peer reviewed and edited by our editorial staff to ensure quality scholarly research articles.
By using this site, you agree to the Terms of Use and Privacy Policy. World Heritage Encyclopedia™ is a registered trademark of the World Public Library Association, a non-profit organization.

Copyright © World Library Foundation. All rights reserved. eBooks from World eBook Library are sponsored by the World Library Foundation,
a 501c(4) Member's Support Non-Profit Organization, and is NOT affiliated with any governmental agency or department.