ALBERT

Description: Secondary organic aerosol (SOA) formation has been investigated as a function of temperature and humidity for the ozone-initiated reaction of the two monoterpenes α-pinene (243–313 K) and limonene (253–313 K) using the 84.5 m3 aerosol chamber AIDA. This paper gives an overview of the measurements done and presents parameters specifically useful for aerosol yield calculations. The ozonolysis reaction, selected oxidation products and subsequent aerosol formation were followed using several analytical techniques for both gas and condensed phase characterisation. The effective densities of the SOA were determined by comparing mass and volume size distributions to (1.25±0.10) g cm−3 for α-pinene and (1.3±0.2) g cm−3 for limonene. The detailed aerosol dynamics code COSIMA-SOA proved to be essential for a comprehensive evaluation of the experimental results and for providing parameterisations directly applicable within atmospheric models. The COSIMA-assisted analysis succeeded to reproduce the observed time evolutions of SOA total mass, number and size distributions by adjusting the following properties of two oxidation product proxies: individual yield parameters (αi), partitioning coefficients (Ki), vapour pressures (pi) and effective accommodation coefficients (γi). For these properties temperature dependences were derived and parameterised. Vapour pressures and partitioning coefficients followed classical Clausius-Clapeyron temperature dependences. From this relationship enthalpies of vaporisation were derived for the two more and less volatile product proxies of α-pinene: (59±8) kJ mol−1 and (24±9) kJ mol−1, and limonene: (55±14) kJ mol−1 and (25±12) kJ mol−1. The more volatile proxy components had a notably low enthalpy of vaporisation while the less volatile proxy components gave enthalpies of vaporisation comparable with those of typical products from α-pinene oxidation, e.g. pinonaldehyde and pinonic acid.

Description: Tropospheric aerosols contain mixtures of inorganic salts, acids, water, and a large variety of organic compounds. Interactions between these substances in liquid mixtures lead to discrepancies from ideal thermodynamic behaviour. By means of activity coefficients, non-ideal behaviour can be taken into account. We present here a thermodynamic model named AIOMFAC (Aerosol Inorganic–Organic Mixtures Functional groups Activity Coefficients) that is able to calculate activity coefficients covering inorganic, organic, and organic–inorganic interactions in aqueous solutions over a wide concentration range. This model is based on the activity coefficient model LIFAC by Yan et al. (1999) that we modified and reparametrised to better describe atmospherically relevant conditions and mixture compositions. Focusing on atmospheric applications we considered H+, Li+, Na+, K+, NH4+, Mg2+, Ca2+, Cl−, Br−, NO3−, HSO4−, and SO42− as cations and anions and a wide range of alcohols/polyols composed of the functional groups CHn and OH as organic compounds. With AIOMFAC, the activities of the components within an aqueous electrolyte solution are well represented up to high ionic strength. Most notably, a semi-empirical middle-range parametrisation of direct organic–inorganic interactions in alcohol + water + salt solutions strongly improves the agreement between experimental and modelled activity coefficients. At room temperature, this novel thermodynamic model offers the possibility to compute equilibrium relative humidities, gas/particle partitioning and liquid–liquid phase separations with high accuracy. In further studies, other organic functional groups will be introduced. The model framework is not restricted to specific ions or organic compounds and is therefore also applicable for other research topics.

Description: Debris flows are very dangerous phenomena claiming thousands of lives and millions of Euros each year over the world. Disaster mitigation includes non-structural (hazard mapping, insurance policies), active structural (drainage systems) and passive structural (check dams, stilling basins) countermeasures. Since over twenty years, many efforts are devoted by the scientific and engineering communities to the design of proper devices able to capture the debris-flow volume and/or break down the energy. If considerable theoretical and numerical work has been performed on the size, the shape and structure of check dams, allowing the definition of general design criteria, it is worth noting that less research has focused on the optimal location of these dams along the debris-flow pathway. In this paper, a methodological framework is proposed to evaluate the influence of the number and the location of the check dams on the reduction of the debris-flow intensity (in term of flow thickness, flow velocity and volume). A debris-flow model is used to simulate the run-out of the debris flow. The model uses the Janbu force diagram to resolve the force equilibrium equations; a bingham fluid rheology is introduced and represents the resistance term. The model has been calibrated on two muddy debris-flow events that occurred in 1996 and 2003 at the Faucon watershed (South French Alps). Influence of the check dams on the debris-flow intensity is quantified taking into account several check dams configurations (number and location) as input geometrical parameters. Results indicate that debris-flow intensity is decreasing with the distance between the source area and the first check dams. The study demonstrates that a small number of check dams located near the source area may decrease substantially the debris-flow intensity on the alluvial fans.

Description: In this paper, we investigate the application of the asynchronous logic approach for the realization of ultra high-speed digital electronics with high complexity. We evaluate the possible physical, technological, and schematical origins of restrictions limiting such an application, and propose solutions for their overcoming. Although our considerations are based on the rapid single-flux quantum technique, the conclusions derived can be generalized about any type of digital information coding.

Description: The build-up of oligomeric compounds during secondary organic aerosol (SOA) formation is subject of atmospheric research since several years. New particle formation and especially the SOA mass yield might be influenced significantly by oligomer formation. However, the chemical nature of observed oligomers and their formation pathways are still unclear. In this paper, the structural characterization of certain dimeric compounds (esters) formed during the ozonolysis of cyclohexene and cyclohexene/α-pinene mixtures are presented. The identification is based on the comparison of the mass spectra and the retention times (LC) of the oligomeric products with synthesized reference compounds. Cyclohexene is used here as a model compound for terpenes as globally most important SOA precursors, since it possesses a simpler structure than the biogenic alkenes and therefore offers the possibility to get access to reference compounds for certain of its oxidation products. In addition to cyclohexene, the formation of esters could also be observed in experiments with α-pinene as reactant.