Laboratory evaluation of the (VIS, IR) scattering matrix of complex-shaped ragweed pollen particles.

Ragweed or Ambrosia artemisiifolia pollen is an important atmospheric constituent affecting the Earth's climate and public health. The literature on light scattering by pollens embedded in ambient air is however rather sparse: polarization measurements are limited to the sole depolarization ratio and pollens are beyond the reach of numerically exact light scattering models mainly due to their tens of micrometre size. Also, ragweed pollen presents a very complex shape, with a small-scale external structure exhibiting spikes that bears some resemblance with coronavirus, but also apertures and micrometre holes. In this paper, to face such a complexity, a controlled-laboratory experiment is proposed to evaluate the scattering matrix of ragweed pollen embedded in ambient air. It is based on a newly-built polarimeter, operating in the infra-red spectral range, to account for the large size of ragweed pollen. Moreover, the ragweed scattering matrix is also evaluated in the visible spectral range to reveal the spectral dependence of the ragweed scattering matrix within experimental error bars. As an output, precise spectral and polarimetric fingerprints for large size and complex-shaped ragweed pollen particles are then provided. We believe our laboratory experiment may interest the light scattering community by complementing other light scattering experiments and proposing outlooks for numerical work on large and complex-shaped particles.

Development of a sampling method for the simultaneous monitoring of straight-chain alkanes, straight-chain saturated carbonyl compounds and monoterpenes in remote areas.

Studies have shown that biogenic compounds, long chain secondary compounds and long lifetime anthropogenic compounds are involved in the formation of organic aerosols in both polluted areas and remote places. This work aims at developing an active sampling method to monitor these compounds (i.e. 6 straight-chain saturated aldehydes from C6 to C11; 8 straight-chain alkanes from C9 to C16; 6 monoterpenes: α-pinene, ß-pinene, camphene, limonene, α-terpinene, & γ-terpinene; and 5 aromatic compounds: toluene, ethylbenzene, meta-, para- and ortho-xylenes) in remote areas. Samples are collected onto multi-bed sorbent cartridges at 200 mL min(-1) flow rate, using the automatic sampler SyPAC (TERA-Environnement, Crolles, France). No breakthrough was observed for sampling volumes up to 120 L (standard mixture at ambient temperature, with a relative humidity of 75%). As ozone has been shown to alter the samples (losses of 90% of aldehydes and up to 95% of terpenes were observed), the addition of a conditioned manganese dioxide (MnO(2)) scrubber to the system has been validated (full recovery of the affected compounds for a standard mixture at 50% relative humidity--RH). Samples are first thermodesorbed and then analysed by GC/FID/MS. This method allows suitable detection limits (from 2 ppt for camphene to 13 ppt for octanal--36 L sampled), and reproducibility (from 1% for toluene to 22% for heptanal). It has been successfully used to determine the diurnal variation of the target compounds (six 3 h samples a day) during winter and summer measurement campaigns at a remote site in the south of France.

Different methods in TiO2 photodegradation mechanism studies: gaseous and TiO2-adsorbed phases.

The development of photocatalysis processes offers a significant number of perspectives especially in gaseous phase depollution. It is proved that the photo-oxidizing properties of photocatalyst (TiO(2)) activated by UV plays an important role in the degradation of volatile organic compounds (VOC). Heterogeneous photocatalysis is based on the absorption of UV radiations by TiO(2). This phenomenon leads to the degradation and the oxidation of the compounds, according to a mechanism that associates the pollutant's adsorption on the photocatalyst and radical degradation reactions. The main objective of the study is the understanding of the TiO(2)-photocatalysis phenomenon including gaseous and adsorbed phase mechanisms. Results obtained with three different apparatus are compared; gaseous phases are analysed and mechanisms at the gaseous phase/photocatalyst interface are identified. This study leads to improve understanding of various mechanisms during pollutant photodegradation: adsorption of pollutants on TiO(2) first takes place, then desorption and/or photodegradation, and finally, desorption of degradation products on TiO(2). The association of analytical methods and different processes makes the determination of all parameters that affect the photocatalytic process possible. Mastering these parameters is fundamental for the design and construction of industrial size reactors that aim to purify the atmosphere.

A global indicator as a tool to follow airborne molecular contamination in a controlled environment.

The impact of pollutants on production quality in nanotechnology necessitates reduction of contaminant levels in cleanrooms. So, devising a global airborne-pollutant indicator (GAPI) for rapid determination of the level of pollution and its danger to the process is justified. This tool used relative impact weights of the different molecules to quantify the pollution. A calculation of impact weight is proposed in this paper. Impact weights could take into account several characteristics of the molecules (molecular volume, sticking coefficient, ...). They could also be combined to be as close as possible to reality. An example of calculations of the impact of molecular volumes on air quality is given.