Short-term storability of volatile organic compounds in bag sampling systems under ambient conditions.

Although bag sampling is a common quantification tool for volatile organic compounds (VOCs), it can serve as a major source of experimental bias, when storing even over a short duration (<24 h). To learn more about the reliability of the bag sampling method, the temporal stability of 27 VOCs (classified into five groups (i.e., aldehydes, nonpolar aromatic hydrocarbons, aliphatic carboxylic acids, phenol and methylphenols, and miscellaneous odorants) is assessed using poly-ester aluminum (PEA) bags at five intervals over a day (0.17, 1, 2, 6, and 24 h). In terms of reproducibility (e.g., relative standard error [RSEt, %]), nonpolar aromatic hydrocarbons (BTXS) exhibit the highest consistency (e.g., average RSE <1.55%). Considerable loss of VOCs is observed in the preparation of gaseous standards from a liquid phase standard when assessed by gas/liquid (G/L) ratio. Further, VOCs with lower molecular weights (e.g., propionaldehyde: 77%-94.4%) and branched molecular structures (e.g., isovaleraldehyde: 67.2%-78.9%) tend to have high G/L ratio (e.g., relative to valeraldehyde: 55.1%-66%). The overall relative recovery (RR; %) values of VOCs indicate an exponential decrease over 24 h. BTXS maintain fairly good RR values (above 94.3% at all intervals), possibly due to the nonpolar structure with uniform distribution of π electrons. In contrast, indole and skatole show the least preservation after 24 h (e.g., RR4 values of 10.9% and 24.6%, respectively) due to their highly reactive characteristics. The storability of VOCs appears to be affected by a number of variables (e.g., molecular weight, presence of ethyl branch, and time: e.g., R2 > 0.9). The results of this study offer valuable guidelines for the accurate quantification of VOC levels in air.

The feasibility and temporal storability of gas phase standards of volatile organic compounds prepared through liquid phase vaporization in polyester aluminum bags at room temperature.

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.