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. Author manuscript; available in PMC: 2013 Mar 9.
Published in final edited form as: J Chromatogr A. 2011 Jul 20;1228:250–262. doi: 10.1016/j.chroma.2011.07.019

Fig. 1.

Fig. 1

Reversed-phase separations of proteins (A) and alkylbenzenes (B) using monolithic poly(styrene-co-divinylbenzene) columns. Conditions: (A) column 50 × 8 mm I.D., mobile phase linear gradient from 20 to 60 % acetonitrile in 0.1 % aqueous trifluoroacetic acid in 24 s, flow rate 25 mL/min; (B) column 100 × 8 mm I.D., mobile phase 70% aqueous acetonitrile, flow rate 1 mL/min. Peaks: ribonuclease A (1), cytochrome c (2), myoglobin (3), ovalbumin (4), benzene (5) ethylbenzene (6), butylbenzene (7).