Decreasing GC Analysis Time with Small Diameter Columns

Application Notes

Decreasing GC Analysis Time with Small Diameter Columns

Shorter, smaller diameter GC capillary columns shown to decrease analysis time by 50% without loss of resolution for PAH\'s, phenols and lemon oil fingerprint compounds.

Decreasing GC Analysis Time with Small Diameter Columns, Alltech Application Note CA001, 1998.

Shorter capillary columns can result in 50% faster GC analysis. Combined with smaller diameters of 100µm or less, the peak resolution and efficiency and hence, the overall resolution can be maintained.

To demonstrate the reduction in time and acceptable resolution achievable using shorter (10m) and smaller diameter capillary columns (0.05-0.10µm), PAHs, phenols and lemon oil components were chromatographed on these type columns and on standard 30m, 0.25µm capillary columns

A comparison of a standard capillary column (AT-5 Capillary, 30m x 0.25mm x 0.25µm, Part No. 13656) with a high efficiency capillary column (AT-5 Hi-Eff Capillary, 10m x 0.05mm x 0.10µm, Part No. 14428) operated under similar conditions with FID detection at 340°C showed that 16 PAHs: (naphthalene, acenaphthalene, acenapthene, fluorene, phenanthrene, anthracene, fluoranthrene, pyrene, benzo(a)anthracene, chrysene, benzo(b)fluoranthrene, benzo(k)fluoranthrene, benzo(a)pyrene, indeno(1,2,3,-cd)pyrene, dibenzo(a,h)anthracene and benzo(ghi)perylene, eluted in less than half the time on the high efficiency column, around 11 minutes.

A similar comparison of 11 phenols (phenol, 2-chlorophenol, 2-nitrophenol, 2,4-dimethylphenol, 2,4-dichlorphenol, 4-chloro-3-methylphenol, 2,4,6-trichlorophenol, 2,4-dinitrophenol, 4-nitrophenol, 2-methyl-4,6-dinitrophenol, and pentachlorophenol) with FID detection at 325°C also showed elution in half the time (11 min. vs. 22).

A lemon oil fingerprint showed a total run time of eight minutes on the high efficiency column with FID detection at 325°C vs. sixteen by the standard column for 27 compounds: a-thulene, a-pinene, camphene, sabinene, b-pinene, 6-methyl-5-hepten-2-one, myrcene, octanal, a-phellandrene, 3-carene, a-terpinene, p-cymene, limonene, g-terpinene, terpinolene, linalool, nonanal, citronellal, terpinen-4-ol, a-terpineol, neral, geranial, neryl acetate, geranyl acetate, b-caryophyllene, trans-a-bergamolene and b-bisabolene.