K-value (VLE)

 

For vapor-liquid equilibrium calculations, the K-value for a component is defined as the mole fraction of the component in the vapor phase divided by the mole fraction of the component in the liquid phase :

  image\THRM01.gif

 

where: image\THERM02.gif = K-value for component i

image\THERM01.gif = mole fraction of component i in the vapor phase

image\THERM03.gif = mole fraction of component i in the liquid phase

 

Equilibrium K-values are usually calculated from fundamental thermodynamic relationships which relate the liquid and vapor fugacities for each component in the mixture. For equation of state methods, the fugacity components are computed directly with the equation of state.

 

Available methods for calculating VLE K-values are listed below. See Section 1.2.1 of the PRO/II Reference Manual for a more complete discussion.

 

Braun-K 10

Grayson-Streed

Improved-Grayson-Streed

Grayson-Streed-Erbar

 

Chao-Seader

Chao-Seader-Erbar

 

Ideal

 

Soave-Redlich-Kwong

SRK-Kabadi-Danner

SRK-Huron-Vidal

SRK-Panag.-Reid

SRK-Modified-Panag.-Reid

SRK-SimSci

SRK-Hexamer

 

Peng-Robinson

PR-Huron-Vidal

PR-Panag.-Reid

PR-Modified Panag.-Reid

 

BWRS

Lee-Kesler-Plocker

UNIWAALS

NRTL

 

Wilson

vanLaar

Margules

Regular Solution

Flory-Huggins

 

UNIQUAC

UNIFAC

UNIFAC TDEP-1 (Lyngby)

UNIFAC TDEP-2 (Dortmund)

UNIFAC TDEP-3

UNIFAC Free Volume

 

Alcohol

Glycol

Sour

GPA Sour Water

Amine

User-added Methods

Electrolyte Models

Advanced Lattice Model

SAFT

PHSC

Predictive Peng-Robinson78