Hochschule für Technik und Umwelt FHNW
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Bereich: Suchergebnisse
Publikation Equation of state and thermodynamic properties for mixtures of H2O,O2, N2, and CO2 from ambient up to 1000 K and 280 MPa(Elsevier, 05.03.2019) Mangold, Fabienne; Pilz, Stephan; Bjelic, Sasa; Vogel, FrédéricSupercritical water oxidation (SCWO) is an effective technique to treat wet organic wastes. Its modeling requires an accurate calculation of thermodynamic properties. In this work an equation of state (EOS) is proposed which accurately predicts the thermodynamic state of mixtures of water, oxygen, nitrogen, and carbon dioxide for a wide range of compositions, temperatures, and pressures including supercritical conditions. The EOS includes a volume translation, an evolved alpha-function and non-quadratic mixing rules. The introduced parameters are regressed to experimental data. From the pressure-explicit EOS, enthalpy, specific heats at constant volume and constant pressure, and fugacity coefficients are derived and calculated. The binary mixtures H2O/O2, H2O/N2, H2O/CO2, N2/CO2 as well as the ternary mixture H2O/O2/N2 are well predicted by the proposed EOS with relative errors below 10% and 15%, respectively. The region of low temperature and high pressure is most difficult to predict with relative errors up to 20%.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Identification of organic acids in secondary organic aerosol and the corresponding gas phase from chamber experiments(American Chemical Society, 15.10.2004) Fisseha, Rebeka; Dommen, Josef; Sax, Mirjam; Paulsen, Dwane; Kalberer, Markus; Maurer, Rolf; Höfler, Frank; Weingartner, Ernest; Baltensperger, UrsOrganic acids in the gas and aerosol phase from photooxidation of 1,3,5-trimethylbenzene in the presence of 300 ppb propene and 300 ppb NOx in smog chamber experiments were determined using a wet effluent diffusion denuder/aerosol collector coupled to ion chromatography (IC) with conductivity detection. Behind the IC, the samples were collected using a fraction collector, for identification of unresolved/unidentified organic acids with IC-mass spectrometry (MS). In total, 20 organic acids were found with MS of which 10 were identified. The organic acids identified offline by IC-MS were then further quantified based on the online IC data. The identification was additionally confirmed with gas chromatography-mass spectrometry. At the maximum aerosol concentration, organic acids comprised 20-45% of the total aerosol mass. The method has a detection limit of 10-100 ng/m3 for the identified carboxylic acids.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Online gas and aerosol measurement of water soluble carboxylic acids in Zurich(Wiley, 2006) Fisseha, Rebeka; Dommen, Josef; Gäggeler, Kathrin; Weingartner, Ernest; Samburova, Vera; Kalberer, Markus; Baltensperger, UrsWe discuss the diurnal and seasonal variability of low molecular weight organic acids in Zurich city on the basis of online quasi‐continuous measurement in the gas and aerosol phase using a wet effluent diffusion denuder/aerosol collector (WEDD/AC) coupled to ion chromatography. The measurements were performed during August–September 2002 and March 2003. Acetic acid exhibited the highest concentration in the gas phase during all the measurement periods, followed by formic acid. Oxalic acid was predominantly found in the aerosol phase and often below the detection limit in the gas phase. In addition, filter samples were analyzed using ion chromatography–mass spectrometry (IC‐MS) to provide more information on organic acids in the aerosol phase. From the offline IC‐MS measurements, 20 monocarboxylic, dicarboxylic, and tricarboxylic acids were determined. In addition, more than 20 different masses were detected with the MS; however, identification of the organic acids was not possible. The sum of the carboxylic acids contributed on average 2% to the water soluble organic carbon (WSOC). The fraction of dicarboxylic acids to the WSOC was higher in summer compared to winter suggesting that dicarboxylic acids are mainly a result of photochemical reactions in summer whereas in winter they mainly result from primary sources.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Seasonal and diurnal characteristics of water soluble inorganic compounds in the gas and aerosol phase in the Zurich area(Copernicus, 2006) Fisseha, Rebeka; Dommen, Josef; Gutzwiller, Lukas; Weingartner, Ernest; Gysel, Martin; Emmenegger, C.; Kalberer, Markus; Baltensperger, UrsGas and aerosol samples were taken using a wet effluent diffusion denuder/aerosol collector (WEDD/AC) coupled to ion chromatography (IC) in the city of Zurich, Switzerland from August to September 2002 and in March 2003. Major water soluble inorganic ions; nitrate, sulfate, and nitrite were analyzed online with a time resolution of two hours for the gas and aerosol phase. The fraction of water soluble inorganic anions in PM10 varied from 15% in August to about 38% in March. Seasonal and diurnal variations of nitrate in the gas and aerosol phase were observed with more than 50% of the total nitrate in the gas phase during August and more than 80% of nitrate in the aerosol phase during March exceeding the concentration of sulfate by a factor of 2. Aerosol sulfate, on the other hand, did not show significant variability with season. However, in the gas phase, the SO2 concentration was 6.5 times higher in winter than in summer. Nitrous acid (HONO) also showed a diurnal variation in both the gas and aerosol phase with the lowest concentration (0.2–0.6 µg/m³) in the afternoon. The primary pollutants, NO, CO and SO2 mixing ratios were often at their highest between 04:00–10:00 local time due to the build up of fresh vehicle emission under a nocturnal inversion.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation On the effects of organic matter and sulphur-containing compounds on the CCN activation of combustion particles(Copernicus, 2005) Petzold, Andreas; Gysel, Martin; Vancassel, Xavier; Hitzenberger, Regina; Puxbaum, Hans; Vrochticky, S.; Weingartner, Ernest; Baltensperger, Urs; Mirabel, PhilippeThe European PartEmis project (Measurement and prediction of emissions of aerosols and gaseous precursors from gas turbine engines) was focussed on the characterisation and quantification of exhaust emissions from a gas turbine engine. The combustion aerosol characterisation included on-line measurements of mass and number concentration, size distribution, mixing state, thermal stability of internally mixed particles, hygroscopicity, cloud condensation nuclei (CCN) activation potential, and off-line analysis of chemical composition. Based on this extensive data set, the role of sulphuric acid coating and of the organic fraction of the combustion particles for the CCN activation was investigated. Modelling of CCN activation was conducted using microphysical and chemical properties obtained from the measurements as input data. Coating the combustion particles with water-soluble sulphuric acid, increases the potential CCN activation, or lowers the activation diameter, respectively. The adaptation of a Köhler model to the experimental data yielded coatings from 0.1 to 3 vol-% of water-soluble matter, which corresponds to an increase in the fraction of CCN-activated combustion particles from ≤10‾⁴ to ≌10‾² at a water vapour saturation ratio Sw=1.006. Additional particle coating by coagulation of combustion particles and aqueous sulphuric acid particles formed by nucleation further reduces the CCN activation diameter. In contrast, particles containing a large fraction of non-volatile organic compounds grow significantly less at high relative humidity than particles with a lower content of non-volatile OC. The resulting reduction in the potential CCN activation with an increasing fraction of non-volatile OC becomes visible as a trend in the experimental data. While a coating of water-soluble sulphuric acid increases the potential CCN activation, or lowers the activation diameter, respectively, the non-volatile organic compounds, mainly found at lower combustion temperatures, can partially compensate this sulphuric acid-related enhancement of CCN activation of carbonaceous combustion aerosol particles.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Non-volatile particle emissions from aircraft turbine engines at ground-idle induce oxidative stress in bronchial cells(Nature, 05.03.2019) Jonsdottir, Hulda R.; Delaval, Mathilde; Leni, Zaira; Keller, Alejandro; Brem, Benjamin T.; Siegerist, Frithjof; Schönenberger, David; Durdina, Lukas; Elser, Miriam; Burtscher, Heinz; Liati, Anthi; Geiser, MarianneAircraft emissions contribute to local and global air pollution. Health effects of particulate matter (PM) from aircraft engines are largely unknown, since controlled cell exposures at relevant conditions are challenging. We examined the toxicity of non-volatile PM (nvPM) emissions from a CFM56-7B26 turbofan, the world’s most used aircraft turbine using an unprecedented exposure setup. We combined direct turbine-exhaust sampling under realistic engine operating conditions and the Nano-Aerosol Chamber for In vitro Toxicity to deposit particles onto air–liquid-interface cultures of human bronchial epithelial cells (BEAS-2B) at physiological conditions. We evaluated acute cellular responses after 1-h exposures to diluted exhaust from conventional or alternative fuel combustion. We show that single, short-term exposures to nvPM impair bronchial epithelial cells, and PM from conventional fuel at ground-idle conditions is the most hazardous. Electron microscopy of soot reveals varying reactivity matching the observed cellular responses. Stronger responses at lower mass concentrations suggest that additional metrics are necessary to evaluate health risks of this increasingly important emission source.01A - Beitrag in wissenschaftlicher ZeitschriftPublikation Characterizing particulate emissions from wood burning appliances including secondary organic aerosol formation potential(Elsevier, 31.08.2017) Keller, Alejandro; Burtscher, HeinzBiomass burning is a major contributor to environmental particulate matter pollution and should therefore be contemplated by emission control legislation. However, policy decisions for improving air quality by imposing emission limits are only as good as the selected metric. We discuss an approach that incorporates recent scientific results and is compatible with type-approval testing and field measurements. We include potential secondary organic aerosol (SOA) by aging emissions in an oxidation flow reactor. Quantification is done by particle-bound total carbon analysis. Total carbon is the fraction relevant to combustion quality and a better marker for toxicity than total particulate matter, which also includes salts and ashes. The data is complemented by on-line size distribution measurements. We exemplify our approach by showing measurements performed on a variety of appliances. Our measurements suggest that non-methane hydrocarbons (NMHC) species with very low volatility are responsible for most of the SOA. Condensing and precipitating this fraction significantly reduces SOA potential but has no noticeable impact on total NMHC. Thus, key precursors of SOA may be a much smaller subset than previously thought. Targeting this fraction could be a straightforward SOA mitigation strategy. These results could not have been derived using the current standard emission control metrics.01A - Beitrag in wissenschaftlicher Zeitschrift