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Electrochemical NOx sensors based on yttria-stabilized zirconia (YSZ) provide a reliable onboard way to control NOx emissions from glass-melting furnaces. The main limitation is the poisoning of this sensor by sulfur oxides (SOx) contained in the stream. To overcome this drawback, an “SO2 trap” with high SOx storage capacity and low affinity to NOx is required. Two CuO/BaO/SBA-15 traps with the same CuO loading (6.5 wt.%) and different BaO loadings (5 and 24.5 wt.%, respectively) were synthetized, thoroughly characterized and evaluated as SO2 traps. The results show that the 6.5%CuO/5%BaO/SBA-15 trap displays the highest SO2 adsorption capacity and can fully adsorb SO2 for a specific period of time, while additionally displaying a very low NO adsorption capacity. A suitable quantity of this material located upstream of the sensor could provide total protection of the NOx sensor against sulfur poisoning in glass-furnace exhausts.

Urban air pollution is partly due to exhaust emissions from road transport. Vehicle emissions have been regulated for more than 30 years in many countries around the world. Each motor type is equipped with a specific emission control system. In gasoline vehicles, a three-way catalytic converter (TWC) is implemented to remove at the same time hydrocarbons (HC), carbon monoxide (CO), and nitrogen oxides (NOx). However, TWCs are only efficient above 200 °C and at a stoichiometric air-to-fuel ratio in the exhaust. However, deviations from stoichiometry occur during fast accelerations and decelerations. This study reports the analysis of unregulated VOCs commercial mini-TWC fed by model gasoline gas mixtures. A synthetic gas bench was used to control the model exhaust containing two model hydrocarbons (propene and propane) to identify the conditions at which VOCs are created under non-optimal conditions. Most of the pollutants such as N2O and VOCs were emitted between 220 and 500 °C with a peak at around 280 °C, temperature which corresponds to the tipping point of the TWC activity. The combination of different mass spectrometric analysis (online and offline) allowed to identify many different VOCs: carbonated (acetone, acetaldehyde, acroleine), nitrile (acetonitrile, propanenitrile, acrylonitrile, cyanopropene) and aromatic (benzene, toluene) compounds. Growth mechanisms from propene and to a lesser extend propane are responsible for the formation of these higher aromatic compounds that could lead to the formation of secondary organic aerosol in a near-field area.

The activity of emission control catalysts must be improved in urban mode at low temperatures. One possible way is to tailor the metal-support interaction between platinum group metals (PGMs) and ceria to stabilize small clusters or single atoms, optimizing the utilization of costly PGMs. In this study, a small loading of Pd (0.45Zr0.10Pr0.45O2−x). After the initial calcination at 800 °C, Pd was mainly in the form of dispersed isolated cations which were found to be efficient for low-temperature CO oxidation but inactive for propane combustion. Nevertheless, a pre-reduction step can trigger the formation of Pd nanoparticles and promote the propane oxidation. Pd nanoparticles, formed during the reduction step, coupled with the high oxygen mobility of CZP45, lead to outstanding catalytic activity for propane oxidation starting from 250 °C. However, the re-oxidation of Pd nanoparticles and their partial re-dispersion, promoted by the fast oxygen mobility of the mixed oxide, rapidly deactivate the catalysts in lean conditions.

Electrochemical NOx sensors based on yttria-stabilized zirconia (YSZ) provide a reliable onboard way to control NOx emissions from glass-melting furnaces. The main limitation is the poisoning of this sensor by sulfur oxides (SOx) contained in the stream. To overcome this drawback, an "SO2 trap" with high SOx storage capacity and low affinity to NOx is required. Two CuO/BaO/SBA-15 traps with the same CuO loading (6.5 wt.%) and different BaO loadings (5 and 24.5 wt.%, respectively) were synthetized, thoroughly characterized and evaluated as SO2 traps. The results show that the 6.5%CuO/5%BaO/SBA-15 trap displays the highest SO2 adsorption capacity and can fully adsorb SO2 for a specific period of time, while additionally displaying a very low NO adsorption capacity. A suitable quantity of this material located upstream of the sensor could provide total protection of the NOx sensor against sulfur poisoning in glass-furnace exhausts. [ABSTRACT FROM AUTHOR]

As part of the FORMES summer 2008 experiment, an Aerodyne compact time-of-flight aerosol mass spectrometer (cToF-AMS) was deployed at an urban background site in Marseille to investigate the sources and aging of organic aerosols (OA). France's second largest city and the largest port in the Mediterranean, Marseille, provides a locale that is influenced by significant urban industrialized emissions and an active photochemistry with very high ozone concentrations. Particle mass spectra were analyzed by positive matrix factorization (PMF2) and the results were in very good agreement with previous apportionments obtained using a chemical mass balance (CMB) approach coupled to organic markers and metals (El Haddad et al., 2011a). AMS/PMF2 was able to identify for the first time, to the best of our knowledge, the organic aerosol emitted by industrial processes. Even with significant industries in the region, industrial OA was estimated to contribute only ~ 5% of the total OA mass. Both source apportionment techniques suggest that oxygenated OA (OOA) constitutes the major fraction, contributing ~ 80% of OA mass. A novel approach combining AMS/PMF2 data with 14C measurements was applied to identify and quantify the fossil and non-fossil precursors of this fraction and to explicitly assess the related uncertainties. Results show with high statistical confidence that, despite extensive urban and industrial emissions, OOA is overwhelmingly non-fossil, formed via the oxidation of biogenic precursors, including monoterpenes. AMS/PMF2 results strongly suggest that the variability observed in the OOA chemical composition is mainly driven in our case by the aerosol photochemical age. This paper presents the impact of photochemistry on the increase of OOA oxygenation levels, formation of humic-like substances (HULIS) and the evolution of α-pinene SOA (secondary OA) components.

In this paper we present the study of catalytic oxidation of volatile organic compound (VOC) traces in air over Pt/γ-Al2O3 catalysts. The study was carried out using a laboratory fixed-bed catalytic reactor (FBCR) with catalytic oxidation of propene and toluene as model reactions. For better understanding of catalytic activity in a FBCR, the influence of operating parameters such as of platinum (Pt) loading, total gas flow rate, VOC concentration, and oxygen content were studied. The results showed that catalytic activity increases with increase in VOC concentration and a decrease in total gas flow rate. This displayed behaviour is instrumental to working at a low temperature region for complete oxidation of volatile organic compounds. Key words: volatile organic compounds, total oxidation, propene, toluene, platinum, alumina Nous presentons dans cet article l'etude de Foxydation catalytique de traces de composes organiques volatils (COV) dans Fair au-dessus de catalyseurs Pt/γ-[Al.sub.2][O.sub.3]. L'etude a ete realisee dans un reacteur catalytique en lit fixe (RCLF) a l'echelle du laboratoire en utilisant l'oxydation catalytique du propene et du toluene comme reactions modeles. Afin de mieux comprendre l'activite catalytique dans le RCLF, nous avons examine l'influence des parameters de fonctionnement tels que la charge en platine (Pt), le debit total de gaz, la concentration en COV et la teneur en oxygene. Les resultats montrent que Factivite catalytique augmente avec Faccroissement de la concentration en COV et la diminution du debit total de gaz. Ce comportement observable est la cld pour Foxydation complete des COV dans les regions a basses temp6ratures. Mots-cles : composes organiques volatils, oxydation totale, propene, toluene, platine, alumine [Traduit par la Redaction], 1. Introduction Volatile organic compounds (VOCs) are emissions from a large variety of sources, but mainly by transport and industrial processes. VOCs constitute hazards to human beings and the environment. [...]