A Novel Method for the Analysis of Volatile Organic Compounds (VOCs) from Red Flour Beetle Tribolium castaneum (H.) using Headspace-SPME Technology

Background: The red flour beetle, Tribolium castaneum (Herbst) (Coleoptera: Tenebrionidae) is one of the world’s most serious stored grain insect pests. A method of early and rapid identification of red flour beetle in stored products is urgently required to improve control options. Specific chemical signals identified as Volatile Organic Compounds (VOCs) that are released by the beetle can serve as biomarkers. Methods: The Headspace Solid Phase Microextraction (HS-SPME) technique and the analytical conditions with GC and GCMS were optimised and validated for the determination of VOCs released from T. castaneum. Results: The 50/30 μm DVB/CAR/PDMS SPME fibre was selected for extraction of VOCs from T. castaneum. The efficiency of extraction of VOCs was significantly affected by the extraction time, temperature, insect density and type of SPME fibre. Twenty-three VOCs were extracted from insects in 4 mL flask at 35 ± 1°C for four hours of extraction and separated and identified with gas chromatography-mass spectroscopy. The major VOCs or chemical signals from T. castaneum were 1-pentadecene, p-Benzoquinone, 2-methyl- and p-Benzoquinone, 2-ethyl. Conclusion: This study showed that HS-SPME GC technology is a robust and cost-effective method for extraction and identification of the unique VOCs produced by T. castaneum. Therefore, this technology could lead to a new approach in the timely detection of T. castaneum and its subsequent treatment.

Ionogel fibres of bis(trifluoromethanesulfonyl)imide anion-based ionic liquids for the headspace solid-phase microextraction of chlorinated organic pollutants

A procedure for the immobilization of different ionic liquids on a SPME fibre was developed and optimized. A hybrid sorbent was successfully applied for the isolation of chlorinated organics from water samples.

New SPME fibre for analysis of mequinol emitted from DVDs

A piece of fused-silica fibre coated with silica modified with ketamine-groups was used as a solidphase microextraction (SPME) fibre and its efficiency in the qualitative and quantitative analysis of volatile organic compounds released from coloured overprinting on DVDs was evaluated. The effect of the parameters that can affect the SPME procedure, such as extraction time, extraction temperature, desorption temperature, was investigated to determine the analytical performance of this novel fibre in the qualitative and quantitative analyses of organic compounds. The optimised procedure was applied to the qualitative and quantitative analyses of organic compounds released from coloured overprinting on DVDs. The limit of detection of 4-methoxyphenol (mequinol) was 88 × 10−3 μg mL−1, while the limit of quantification (LOQ) was calculated as ten times the baseline noise, i.e. 3.1 × 10−1 μg mL−1. The proposed fibre was used successfully for preconcentration of the volatile organic compounds from the gaseous phase of DVD samples.

Quantitative and enantioselective analysis of monoterpenes from plant chambers and in ambient air using SPME

A headspace solid-phase microextraction (HS-SPME) and gas chromatography/mass spectrometry (GC/MS) system has been developed for quantifying enantiomeric and nonenantiomeric monoterpenes in plant chamber studies and ambient air. Performance of this system was checked using a capillary diffusion system to produce monoterpene standards. The adsorption efficiency, competitive adsorption and chromatographic peak resolution of monoterpene enantiomer pairs were compared for three SPME fibre coatings: 75 μm Carboxen-PDMS (CAR-PDMS), 50/30 μm divinylbenzene-carboxen-polydimethylsiloxane (DVB-CAR-PDMS) and 65 μm divinylbenzene-polydimethylsiloxane (DVB-PDMS). Key parameters such as the linearity and reproducibility of the SPME system have been investigated in this work. The best compromise between the enantiomeric separation of monoterpenes and competitive adsorption of the isoprenoids on the solid SPME fibre coating was found for DVB-PDMS fibres. The optimum conditions using DVB-PDMS fibres were applied to measure the exchange rates of monoterpenes in the emission of Quercus ilex using a laboratory whole plant enclosure under light and dark conditions, as well as in ambient air. With 592 and 223 ng m−2 s−1 respectively, β-myrcene and limonene were the predominant monoterpenes in the emission of Q. ilex. These values were closely comparable to those obtained using a zNose and cartridge GC-FID systems.

Quantitative and enantioselective analysis of monoterpenes from plant chambers and in ambient air using SPME

A solid-phase microextraction (HS-SPME) and gas chromatography/mass spectrometry (GC/MS) system has been developed for quantifying enantiomeric and nonenantiomeric monoterpenes in plant chamber studies and ambient air. Performance of this system was checked using a capillary diffusion system to produce monoterpene standards. The adsorption efficiency, competitive adsorption and chromatographic peak resolution of monoterpene enantiomer pairs were compared for three SPME fibre coatings: 75 μm Carboxen-PDMS (CAR-PDMS), 50/30 μm, divinylbenzene-carboxen-polydimethylsiloxane (DVB-CAR-PDMS) and 65 μm divinylbenzene-polydimethyl-siloxane (DVB-PDMS). Key parameters such as the linearity and reproducibility of the SPME system have been investigated in this work. The best compromise between the enantiomeric separation of monoterpenes and competitive adsorption of the isoprenoids on the solid SPME fibre coating was found for DVB-PDMS fibres. The optimum conditions using DVB-PDMS fibres were applied to measure the exchange rates of monoterpenes in the emission of Quercus ilex using a laboratory whole plant enclosure under light and dark conditions, as well as in ambient air. With 592 and 223 ng m−2 s−1, respectively, β-myrcene and limonene were the predominant monoterpenes in the emission of Q. ilex. These values were closely comparable to those obtained using a zNose and cartridge GC-FID systems.

Fast determination of methyl chloride and methyl bromide emissions from dried plant matter and soil samples using HS-SPME and GC-MS: method and first results

Environmental context. Headspace solid-phase microextraction (HS-SPME) and analysis by gas chromatography–mass spectrometry (GC/MS) system has been employed for quantifying the emissions of methyl chloride (CH3Cl) and methyl bromide (CH3Br) from plants and soils. Compared with more commonly used techniques, HS-SPME coupled to GC/MS is simple, fast, sensitive, economical and non-destructive, with potential for laboratory-based and field studies. Abstract. Headspace solid-phase microextraction (HS-SPME) and gas chromatography–mass spectrometry (GC/MS) system have been employed for quantifying the emissions of methyl chloride (CH3Cl) and methyl bromide (CH3Br) from plants and soils. Seven SPME fibre coatings including 75 μm Carboxen-polydimethylsiloxane (CAR-PDMS), 85 μm Carboxen-PDMS (CAR-PDMS), 50/30 μm divinylbenzene-CAR-PDMS (DVB-CAR-PDMS), 65 μm DVB-PDMS, 65 μm carbowax-DVB (CW-DVB), 30 μm PDMS (PDMS) and 100 μm PDMS, were tested by comparing their sampling efficiencies towards CH3Cl and CH3Br. Key parameters such as extraction time, desorption temperature and time were all optimised in this work. The optimum conditions were found with CAR-PDMS 75 μm as an SPME fibre coating, a 1-min sampling time, a 50°C incubation temperature and a 2-min desorption time and a 250°C desorption temperature. These conditions were used for the determination of CH3Cl and CH3Br emission rates from different plant species as well as soil samples. Compared with more commonly used techniques, HS-SPME coupled to GC/MS is simple, fast, sensitive, economical and non-destructive, with potential for laboratory-based and field studies.