Skip to main navigation Skip to search Skip to main content

An exploration on the suitability of airborne carbonyl compounds analysis in relation to differences in instrumentation (GC-MS versus HPLC-UV) and standard phases (Gas versus Liquid)

  • Ki Hyun Kim*
  • , Jan E. Szulejko
  • , Yong Hyun Kim
  • , Min Hee Lee
  • *Corresponding author for this work
  • Hanyang University

Research output: Contribution to journalJournal articlepeer-review

Abstract

The relative performance figure of merits was investigated for the two most common analytical methods employed for carbonyl compounds (CC), for example, between high performance liquid chromatography (HPLC)-UV detector (with 2,4-dinitrophenylhydrazine (DNPH) derivatization) and thermal desorption (TD)-gas chromatography (GC)-mass spectrometry (MS) (without derivatization). To this end, the suitability of each method is assessed by computing the relative recovery (RR) between the gas- and liquid-phase standards containing a suite of CC such as formaldehyde (FA), acetaldehyde (AA), propionaldehyde (PA), butyraldehyde (BA), isovaleraldehyde (IA), and valeraldehyde (VA) along with benzene (B) as a recovery reference for the GC method. The results confirm that a TD-GC-MS is advantageous to attain the maximum recovery for the heavier CCs (i.e., with molecular weights (MW) above BA-MW ≥ 74). On the other hand, the HPLC-UV is favorable for the lighter CCs (like FA and AA) with the least bias. Such compound-specific responses for each platform are validated by relative ordering of CCs as a function of response factor (RF), method detection limit (MDL), and recovery pattern. It is thus desirable to understand the advantages and limitations of each method to attain the CC data with the least experimental bias.

Original languageEnglish
Article number308405
JournalThe Scientific World Journal
Volume2014
DOIs
StatePublished - 2014

Fingerprint

Dive into the research topics of 'An exploration on the suitability of airborne carbonyl compounds analysis in relation to differences in instrumentation (GC-MS versus HPLC-UV) and standard phases (Gas versus Liquid)'. Together they form a unique fingerprint.

Cite this