are specific interactions with a solute, e.g. on a nonpolar stationary phase,
t-butyl alcohol (bp 82.6∞C) elutes before cyclohexane (bp 80.8∞C) because
the latter, being nonpolar itself, dissolves better in the stationary phase.
However, on a polar stationary phase with hydroxy groups, the elution order
is reversed because the alcohol can H-bond to it.Selections of stationary phases are given in Tables 3 and 4.144 Section D – Separation techniques
036912
Time (min)15 18 21 2412
345678
9
10Inject012346
7(^89)
10
12
11
40 min
13
14
15
16
17
Peak indentification
- pyridine
- 2,4,5-trimethyloxazole
- 3-methylpyridine
- 1-pentanol
- ethylheptanoate
- 1-hexanol
- 1-heptanol
- linaloate
- 1-octanol
- 1-nonanol
- citronellol
- 1-decanol
- 3-acetylpyridine
- anisaldehyde
- cinnamaldehyde
- d-decalactone
- anisylalcohol
5Fig. 4. Examples of gas chromatographic separations on capillary and packed columns. (a) Packed column separation
of mixed hydrocarbons; (b) capillary column separation of some flavor compounds. Reproduced from D.W. Grant,
Capillary Gas Chromatography, 1996. © John Wiley & Sons Ltd. Reproduced with permission.
(a) Peak indentification
- isopentane
- n-pentane
- cyclopentane
- 3-methylpentane
- n-hexane
- 2,4-dimethylpentane
- benzene
- cyclohexane
- 3-methylhexane
- n-heptane
(b)