Currently, the presence of many classes of volatile organic compounds (VOCs) in indoor air is well recognized. There is an impetus to accurately quantify airborne VOCs for the proper assessment of their human health risks. VOC standards prepared in a solvent are often vaporized in N2 gas-filled sampling bags for external calibration as the use of grab sampling bags is a common practice for the collection of real ambient air samples. Such practices can nontheless be subject to many sources of biases in their calibration (e.g., VOC chemical reaction with the solvent, adsorption on the bag interior surface, or leakage). The main goal of this work is to measure the temporal stability of 11 VOC targets (benzene, toluene, o-xylene, styrene, propionaldehyde, n-butyraldehyde, isovaleraldehyde, valeraldehyde, acrylonitrile, isoprene, and methyl ethyl ketone) selected in this research over 24 h which started 10 min after the injection and vaporization of liquid-phase standards (all prepared in methanol solvent) into polyester aluminum (PEA) bags containing 1 atm N2. Although all tested VOCs showed gradual decreases of their concentrations (e.g., >17% in 24 h), the aromatic hydrocarbon VOCs (namely BTXS) yielded the best relative recoveries (e.g., decreases of 11%-30% in 24 h) and relative errors (e.g., relative standard error (RSE) = 2.14-3.59%) in 5 replicate tests. A good linear relationship was established between the 24 h VOC relative recovery and molecular weight (R2 > 0.81). The results of this study offers valuable clues to properly reduce the bias in the calibration of gas-phase VOC standards when calibrating the system through the vaporization of liquid-phase VOC standards prepared in a solvent.
Keywords: Air sampling; Polyester aluminum bag; Response factor; Storage stability; Vaporization; Volatile organic compounds.
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