Kovats retention index
In gas chromatography, Kovats retention index (shorter Kovats index, retention index; plural retention indices) is used to convert retention times into system-independent constants. The index is named after the Hungarian-born Swiss chemist Ervin Kováts, who outlined this concept during the 1950s while performing research into the composition of the essential oils.[1]
The retention index of a chemical compound is retention time interpolated between adjacent n-alkanes. While retention times vary with the individual chromatographic system (e.g. with regards to column length, film thickness, diameter and inlet pressure), the derived retention indices are quite independent of these parameters and allow comparing values measured by different analytical laboratories under varying conditions and analysis times from seconds to hours. Tables of retention indices are used to identify peaks by comparing measured retention indices with the tabulated values.[2][3][4]
Isothermal Kovats retention index
The Kovats index applies to organic compounds. The method interpolates peaks between bracketing n-alkanes. Kovats index of n-alkanes is 100 times their carbon number, e.g. the Kovats index of n-Butane is 400. The Kovats index is dimensionless, contrary to retention time or retention volume. For isothermal gas chromatography, the Kovats index is given by the equation:
Symbols stand for:
- the Kováts retention index of peak i
- carbon number of n-alkane peak heading peak i
- retention time of compound i, minutes
- air peak, void time in average velocity , minutes
The Kovats index also applies to packed columns with an equivalent equation:
Kovats index and Physical Properties
Compounds elute in the carrier gas phase only. Compounds solved in the stationary phase stay put. The ratio of gas time and residence time in the stationary liquid polymer phase is called the capacity factor :
- ß
Symbols represent physical properties:
- gas constant (8.314J/mole/k)
- temperature [k]
- solubility of compound i in polymer stationary phase [mole/m3]
- vapor pressure of pure liquid i [Pa]
Capillary tubes with uniform coatings have this phase ratio ß:
- ß
Capillary inner diameter is well defined but film thickness reduces by bleed and thermal breakdown that occur after column heating over time, depending on chemical bonding to the silica glass wall and polymer cross-linking of the stationary phase. Above capacity factor can be expressed explicit for retention time:
Retention time is shorter by reduced over column life time. Column length is introduced with average gas velocity :
and temperature have a direct relation with . However, warmer columns ↑ do not have longer but shorter, following temperature programming experience. Pure liquid vapor pressure rises exponentially with so that we do get shorter warming the column ↑. Solubility of compounds in the stationary phase may rise or fall with , but not exponentially. is referred to as selectivity or polarity by gas chromatographers today. Isothermal Kovats index in terms of the physical properties becomes:
Isothermal Kovats index is independent of , any GC dimension or ß or carrier gas velocity , which compares favorable to retention time . Isothermal Kovats index is based on solubility and vapor pressure of compound i and n-Alkanes (). dependence depends on the compound compared to the n-alkanes. Kovats index of n-alkanes is independent of . Isothermal Kovats indices of hydrocarbon were measured by Axel Lubeck and Donald Sutton.[5]
Temperature Programmed Kovats index
IUPAC defines the temperature programmed chromatography Kovats index equation:
- & retention times of heading and trailing n-alkanes.
NOTE: TPGC index does depend on temperature program, gas velocity and the column used !
Measured Kovats retention index values can be found in ASTM method D 6730 databases. An extensive Kovats index database is compiled by NIST .
Method Translation
Faster GC methods have shorter times but Kovats indexes of the compounds may be conserved if proper method translation is applied. Temperatures of the temperature program stay the same, but ramps and times change when using a smaller column or faster carrier gas. If column dimensions Length×diameter×film are divided by 2 and gas velocity is doubled by using H2 in place of He, the hold times must be divided by 4 and the ramps must be multiplied by 4 to keep the same index and the same retention temperature for the same compound analyzed. Method translation rules are incorporated in some chromatography data systems.
References
- Institute of Chemical Sciences and Engineering, KOVATS Ervin, Prof. Hon.
- Kovats, E. (1958). "Gas-chromatographische Charakterisierung organischer Verbindungen. Teil 1: Retentionsindices aliphatischer Halogenide, Alkohole, Aldehyde und Ketone". Helv. Chim. Acta. 41 (7): 1915–32. doi:10.1002/hlca.19580410703.
- IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "retention index, I in column chromatography". doi:10.1351/goldbook.R05360
- Retention index guide
- [J.o.Hi.Res.Chro.(1982,1983)Data Cards]