3.6. Gas Chromatography and Mass Spectrometry Analysis of VOCs

IJ Igor Jerković
MK Marina Kranjac
ZM Zvonimir Marijanović
Bojan Šarkanj
AC Ana-Marija Cikoš
KA Krunoslav Aladić
SP Sandra Pedisić
SJ Stela Jokić
request Request a Protocol
ask Ask a question
Favorite

The GC-FID analyses of volatiles were carried out with an Agilent Technologies (Palo Alto, CA, USA) gas chromatograph model 7890A equipped with a flame ionization detector (FID) and a HP-5MS capillary column (5% phenyl-methylpolysiloxane, Agilent J and W). The GC-MS analyses were performed on an Agilent Technologies (Palo Alto, CA, USA) gas chromatograph model 7890A equipped with a mass selective detector (MSD) model 5977E (Agilent Technologies) and HP-5MS capillary column, under the same conditions as for the GC-FID analysis. The GC conditions and the detail procedure are described in our previously published paper [53]. The identification of the compounds was based on the comparison of their retention indices (RI), determined relative to the retention times of C9–C25 homologous series of n-alkanes with those reported in the literature and on the comparison of their mass spectra with available authentic compounds or with the mass spectra listed in Wiley 9 (Wiley, New York, NY, USA) and NIST 14 (D-Gaithersburg) mass spectral libraries. The percentage composition of the samples was computed from the GC peak areas using the normalization method (without correction factors). The average component percentages in Table 1 were calculated from duplicate GC-FID and GC-MS analyses. One-way analysis of variance (ANOVA) and multiple comparisons (Duncan’s post-hoc test) were used to evaluate the significant difference of the data at p < 0.05 (Table 1.).

Do you have any questions about this protocol?

Post your question to gather feedback from the community. We will also invite the authors of this article to respond.

post Post a Question
0 Q&A