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Wood burning is widely used for domestic heating and has been identified as a ubiquitous pollution source in urban areas, especially during cold months. The present study is based on a three and a half winter months field campaign in the Paris region measuring Volatile Organic Compounds (VOCs) by Proton Transfer Reaction Mass Spectrometry (PTR-MS) in addition to Black Carbon (BC). Several VOCs were identified as strongly wood burning-influenced (e.g., acetic acid, furfural), or traffic-influenced (e.g., toluene, C8-aromatics). Methylbutenone, benzenediol and butandione were identified for the first time as wood burning-related in ambient air. A Positive Matrix Factorization (PMF) analysis highlighted that wood burning is the most important source of VOCs during the winter season. (47%). Traffic was found to account for about 22% of the measured VOCs during the same period, whereas solvent use plus background accounted altogether for the remaining fraction. The comparison with the regional emission inventory showed good consistency for benzene and xylenes but revisions of the inventory should be considered for several VOCs such as acetic acid, C9-aromatics and methanol. Finally, complementary measurements acquired simultaneously at other sites in Île-de-France (the Paris region) enabled evaluation of spatial variabilities. The influence of traffic emissions on investigated pollutants displayed a clear negative gradient from roadside to suburban stations, whereas wood burning pollution was found to be fairly homogeneous over the region., (Copyright © 2019 Elsevier B.V. All rights reserved.)

During the European Life+ project PhotoPAQ (Demonstration of Photocatalytic remediation Processes on Air Quality), photocatalytic remediation of nitrogen oxides (NOx), ozone (O3), volatile organic compounds (VOCs), and airborne particles on photocatalytic cementitious coating materials was studied in an artificial street canyon setup by comparing with a colocated nonactive reference canyon of the same dimension (5 × 5 × 53 m). Although the photocatalytic material showed reasonably high activity in laboratory studies, no significant reduction of NOx, O3, and VOCs and no impact on particle mass, size distribution, and chemical composition were observed in the field campaign. When comparing nighttime and daytime correlation plots of the two canyons, an average upper limit NOx remediation of ≤2% was derived. This result is consistent only with three recent field studies on photocatalytic NOx remediation in the urban atmosphere, whereas much higher reductions were obtained in most other field investigations. Reasons for the controversial results are discussed, and a more consistent picture of the quantitative remediation is obtained after extrapolation of the results from the various field campaigns to realistic main urban street canyon conditions.

Within the framework of the European Life+-funded project PhotoPAQ (Demonstration of Photocatalytic remediation Processes on Air Quality), which was aimed at demonstrating the effectiveness of photocatalytic coating materials on a realistic scale, a photocatalytic de-polluting field site was set up in the Leopold II tunnel in Brussels, Belgium. For that purpose, photocatalytic cementitious materials were applied on the side walls and ceiling of selected test sections inside a one-way tunnel tube. This article presents the configuration of the test sections used and the preparation and implementation of the measuring campaigns inside the Leopold II tunnel. While emphasizing on how to implement measuring campaigns under such conditions, difficulties encountered during these extensive field campaigns are presented and discussed. This included the severe de-activation observed for the investigated material under the polluted tunnel conditions, which was revealed by additional laboratory experiments on photocatalytic samples that were exposed to tunnel air. Finally, recommendations for future applications of photocatalytic building materials inside tunnels are given., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

Rate constants for the gas-phase reactions of the NO(3) radical with a series of unsaturated aldehydes, trans-2-hexenal, trans-2-heptenal, and trans-2-octenal, have been measured using absolute rate method at 294 ± 3 K and atmospheric pressure. This work was performed to clarify discrepancies found in the literature and thus led to a clearer view of the effect of the increasing carbon chain length on the reactivity of trans-2-alkenals. The rate constants were determined to be (4.7 ± 1.5) × 10(-15), (5.3 ± 1.6) × 10(-15), and (5.6 ± 2.3) × 10(-15) cm(3) molecule(-1) s(-1) for trans-2-hexenal, trans-2-heptenal, and trans-2-octenal, respectively. These results clearly indicate that the carbon chain lengthening of the trans-2-alkenals does not significantly affect the rate constant. In addition, the mechanism for the reaction of NO(3) with these unsaturated aldehydes was also investigated. Unsaturated peroxynitrate-type compounds that are exclusively formed through the abstraction channel were observed as the main products.