Terry Zhang and Guifeng Jiang, Thermo Fisher Scientific, San Jose, California, USA.
Carbonyl compounds from motor vehicle and industrial emissions, precursors to ground-level ozone, are also sources of pollution
in indoor living and working environments.
HPLC coupled with UV detection is the most widely recognized technique for the analysis of carbonyl-DNPH derivatives.
LC separations were performed on a Thermo Scientific Accela 1250 UHPLC system which offers the flexibility of performing both
HPLC and UHPLC separations on a single platform. The Accela 1250 Pump delivers precise flows and accurate gradients at an
expansive range of flow rates (up to 2 mL/min) and pressures (up to 1250 bar); and accelerates method development and maximizes
method flexibility through quaternary gradient capabilities. The Accela UHPLC system together with Thermo Scientific 1.9 μm
Hypersil GOLD C18 columns enables fast chromatographic separations with high efficiency and resolution.
The use of sub-2 μm particle columns facilitates rapid analysis of challenging samples by improving chromatographic resolution,
speed and sensitivity. Using the Accela 1250 UHPLC system, a single Hypersil GOLD C18 column (1.9 μm, 2.1 × 100 mm) and a
simple acetonitrile/water gradient, a mixture of the DNPH standards of 12 carbonyls targeted by US EPA Method 8315A Procedure
1 was successfully separated. This analysis was performed using a flow rate of 800 μL/minute, which generated back pressures
over 1000 bar. The Accela 1250 pump is the only commercially available LC platform that is capable of handling such high operational
pressures due to its very low internal back pressures.
Figure 1 demonstrates UHPLC separation of the 15 carbonyl-DNPH derivatives using the Hypersil GOLD C18 column and a 13-minute
gradient. All compounds but the tolualdehyde isomers were baseline resolved.
Figure 1: UHPLC separation of 15 carbonyl-DNPH derivatives at 20 μg/mL concentrations using a Hypersil GOLD C18 column and
Excellent linearity in detector response was observed over the range of 98–50000 ng/mL (ppb) [196–100000 ng/mL (ppb) for m-
and p-tolualdehyde combined], with correlation coefficients greater than 0.999 for all analytes.
Reproducibility and Accuracy
Reproducibility was investigated by analysing five replicate injections of each analyte. With four channel mixings of the
solvents at various viscosities, retention time RSDs ranged from 0.52–2.22% while peak area RSDs ranged from 0.46–4.91%, indicating
excellent method reproducibility, particularly of the LC pump.
Quantitative accuracy for all carbonyl-DNPH derivatives was evaluated at two levels of concentrations, 400 ppb and 2000 ppb,
using external calibration method. The accuracy of two representative analytes, benzaldehyde-DNPH and o-tolualdehyde-DNPH
are reflected by the values of 96.3% and 103.6% at 400 ppb, respectively, and 99.8% and 99.9% at 2000 ppb, respectively and
achieved with the UHPLC method.