The emergence of new super-insulated buildings to reduce energy consumption places the quality of indoor air at the center of the debate. Among the indoor air pollutants, aldehydes are often present, and formaldehyde is of major interest regarding its multiple sources and its health impact. Therefore, French regulations expect to reduce formaldehyde concentrations below 10 µg m −3 in public buildings by 2023. Formaldehyde and other aldehydes were measured for two weeks during an intensive field campaign conducted in a school recently built and equipped with programmable dual-flow ventilation. Aldehydes were monitored with the ISO 16000-3 reference method based on sampling with 2,4-dinitrophenylhydrazine (DNPH) tubes while formaldehyde concentration was continuously measured by using a sensitive near real-time formaldehyde microanalyzer with a detection limit of 1 µg m −3 . Formaldehyde was the major aldehyde. Its concentrations varied in the range of 2-25 µg m −3 and decreased by half when mechanical ventilation was ON, while the other ones were always below 5 µg m −3 . In addition, an excellent agreement was observed between the different analytical techniques deployed to quantify formaldehyde levels. The microanalyzer was able to measure fast variations of formaldehyde concentration in the studied room, according to the building's ventilation periods.

BTEX compounds are of particular interest, above all benzene because it is a carcinogenic compound for which guideline value in European indoor environments is set to 1.6 ppb. Therefore, the detection of such relatively low value requires the use of particularly sensitive analytical techniques.Several existing chromatographic techniques, such as fast and transportable Gas Chromatograph with Photoionization Detection (GC-PID) or sedentary chromatographic-based techniques equipped with a thermo-desorption device (ATD) and coupled to either Flame Ionization Detection (FID) or Mass Spectrometry (MS), can quantify benzene and its derivatives at such low levels. These instruments involve different injection modes, i.e. on-line gaseous sampling or thermodesorption of adsorbent tubes spiked with liquid or gas samples. In this study, the performances of 3 various analytical techniques mentioned above were compared in terms of sensitivity, linearity, accuracy and repeatability for the 6 BTEX. They were also discussed related to their analyses time consumption or transportability. The considered analytical techniques are ATD-GC-FID, ATD-GC-MS where both Full scan and SIM mode were tested and a transportable GC-PID. For benzene with on-line injection, Limits of Detection (LOD) were significantly below the European guideline with values of 0.085, 0.022, 0.007 and 0.058 ppb for ATD-GC-FID, ATD-GC-MS in full scan mode, ATD-GC-MS in SIM mode and transportable GC-PID, respectively. LOD obtained with adsorbent tubes spiked with liquid standards were approximately the same order of magnitude.

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Most of Polycyclic Aromatic Hydrocarbons (PAHs) are associated to airborne particles and their health impact depends on the particle size where they are bound. This work aims to develop a high sensitive analytical technique to quantify particulate PAHs sampled with a 3-stages cascade impactor in order to derive simultaneously their individual concentration in PM1, PM2.5 and PM10. Three key steps of the method were evaluated separately in order to avoid any PAHs loss during the global sample preparation procedure: (1) the accelerated solvent extraction of PAHs from the filter; (2) the primary concentration of the extract until 1 mL by means of a rotary evaporator at 45°C and 220 mbar and (3) the final concentration of the pre-concentrated extract to about 100-150 µL under a gentle nitrogen stream. Each recovery experiment was realized in triplicates. All these steps evaluated independently show that the overall PAHs loss, even for those with a low molecular weight, should not exceed more than a few percent. Extracts were then analyzed by using a HPLC coupled to fluorescence and Diode Array Detectors with the external standard method. The resulting calibration curves containing between 9 and 12 points were plotted in the concentration range of 0.05-45 µg L(-1) for most of the 16 US-EPA priority PAHs and were fully linear (R(2)>0.999). Limits Of Quantification were in the range 0.05-0.47 µg L(-1) corresponding to 0.75-7.05 pg m(-3) for 20 m(3) of pumped air. Finally, taking into account the average PAHs concentrations previously reported in typical European indoor environments, and considering the use of a 3-stages cascade impactor to collect simultaneously PM>10 µm, 2.5 µm

New efficient approaches to the characterization of fly ash and particulate matter (PM) have to be developed in order to better understand their impacts on environment and health. Polycyclic aromatic hydrocarbons (PAH) contained in PM from biomass burning have been identified as genotoxic and cytotoxic, and some tools already exist to quantify their contribution to PM. Optical fluorescence microscopy is proposed as a rapid and relatively economical method to allow the quantification of PAH in different particles emitted from biomass combustion. In this study samples were collected in the flue gas of biomasscombustion facilities with nominal output ranging from 40 kW to 17.3 MW. The fly ash samples were collected with various flue gas treatment devices (multicyclone, baghouse filter, electrostatic precipitator); PM samples were fractionated from the flue gas with a DEKATI Ò DGI impactor. A method using fluorescence observations (at 470 nm), white-light observations and image processing has been developed with the aim of quantifying fluorescence per sample. Organic components of PM and fly ash, such as PAH, humic-like substances (HULIS) and water-soluble organic carbon (WSOC) were also quantified. Fluorescence microscopy analysis method assessment was first realized with fly ash that was artificially coated with PAH and HULIS. Total amounts of PAH in the three size fractions of actual PM from biomass burning strongly correlated with the intensities of fluorescence. These encouraging results contribute to the development of a faster and cheaper method of quantifying particle-bound PAH.

An analytical method associating accelerated solvent extraction (ASE) and solid-phase micro-extraction (SPME) in immersion mode combined with gas chromatography dual electrons capture detectors (SPME-GC-2ECD) has been developed and studied for the simultaneous determination of 19 organochlorine pesticides (OCPs) and 22 polychlorinated biphenyls (PCBs) in air samples (active and XAD-2 passive samplers). Samples were extracted with ASE with acetonitrile using the following conditions: temperature, 150 °C; pressure, 1500 psi; static, 15 min; cycles, 3; purge, 300 s; flush, 100 %. Extracts were reduced to 1 mL, and 500 μL of this extract, filled with deionised water, was subject to SPME extraction. Experimental results indicated that the proposed method attained the best extraction efficiency under the optimised conditions: extraction of PCB-OCP mixture using 100-μm PDMS fibre at 80 °C for 40 min with no addition of salt. The performance of the proposed ASE-SPME-GC-2ECD methodology with respect to linearity, limit of quantification and detection was evaluated by spiking of XAD-2 resin with target compounds. The regression coefficient (R (2)) of most compounds was found to be high of 0.99. limits of detection (LODs) are between 0.02 and 4.90 ng m(-3), and limits of quantification (LOQs) are between 0.05 and 9.12 ng m(-3) and between 0.2 and 49 ng/sampler and 0.52 and 91 ng/sampler, respectively, for XAD-2 passive samplers. Finally, a developed procedure was applied to determine selected PCBs and OCPs in the atmosphere.

The emergence of new super-insulated buildings to reduce energy consumption can lead to a degradation of the indoor air quality. While some studies were carried out to assess the air quality in these super-insulated buildings, they were usually focused on the measurement of gas phase pollutants such as carbon dioxide and volatile organic compounds. This work reports the first measurements of Polycyclic Aromatic Hydrocarbons (PAHs) associated with particles as a function of time and particle size in a low-energy building. The airborne particles were collected indoors and outdoors over three to four days of sampling using two three-stage cascade impactors allowing to sample simultaneously particles with aerodynamic diameter Dae > 10 µm, 2.5 µm < Dae < 10 µm, 1 µm < Dae < 2.5 µm, and Dae < 1 µm. The 16 US-EPA priority PAHs were then extracted and quantified by high-performance liquid chromatography (HPLC) coupled to fluorescence detection. The resulting total particle concentrations were low, in the ranges 3.73 to 9.66 and 0.60 to 8.83 µg m-3 for indoors and outdoors, respectively. Thirteen PAHs were always detected in all the samples. The total PAH concentrations varied between 290 and 415 pg m−3 depending on the particle size, the environment (indoors or outdoors) and the sampling period considered. More interestingly, the temporal variations of individual PAHs highlighted that high molecular weight PAHs were mainly associated to the finest particles and some of them exhibited similar temporal behaviors, suggesting a common emission source. The indoor-to-outdoor concentration ratios of individual PAH were usually found close to or less than 1, except during the event combining rainy conditions and limited indoor ventilation rate.

In Beirut–Rafic Hariri International Airport (RHIA), airport employees stay at least 12 h inside the airport’s buildings and suffer from respiratory symptoms. Additionally, direct openings exist between the apron and the arrivals hall providing a pathway for contaminated air to enter the buildings. Hence, we study the impact of Beirut–RHIA’s activities on the indoor air of the arrivals hall (impact on employees and passengers) during June, November, and October 2014. Due to their impacts on air quality and human health, assessing of the concentrations of nitrogen dioxide (NO2) and Volatile Organic Compounds (VOCs) was the target of our study by using gas chromatographic techniques (GC-MS and GC-FID) for VOCs and calorimetric methods for NO2 concentrations. NO2 levels indicated a probable hazard to the health of passengers and employees, while measured VOC levels did not present any risks except for acrolein. This is the first study to assess the speciation of a large number of VOCs (46 VOCs) for airport indoor air while revealing a very interesting correlation between aircraft number and the concentrations of VOC groups (namely heavy alkanes, aldehydes and ketones, and monoaromatics). Moreover, this is the first study in Lebanon to assess the speciation of a large number of VOCs in indoor air.