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Mobility particle size spectrometers (MPSS) belong to the essential instruments in aerosol science that determine the particle number size distribution (PNSD)in the submicrometer size range. Following calibration procedures and target uncertainties against standards and reference instruments are suggested for a complete MPSS quality assurance program: a) calibration of the CPC counting efficiency curve (within 5% for the plateau counting efficiency; within 1 nm for the 50% detection efficiency diameter), b) sizing calibration of the MPSS, using a certified polystyrene latex (PSL) particle size standard at 203 nm (within 3%), c) intercomparison of the PNSD of the MPSS (within 10% and 20% of the dN/dlogDP concentration for the particle size range 20 – 200 nm and 200 to 800 nm, respectively), and d) intercomparison of the integral PNC of the MPSS (within 10%). Furthermore, following measurement uncertainties have been investigated: a) PSL particle size standards in the range from 100-500nm match within 1% after sizing calibration at 203 nm. b) Bipolar diffusion chargers based on the radioactive nuclides Kr85, Am241 and Ni63 and a new ionizer based on corona discharge follow the recommended bipolar charge distribution, while soft X-ray-based charges may alter faster than expected. c) The use of a positive high voltage supply show a 10% better performance than a negative one. d) The intercomparison of the integral PNC of an MPSS against the total number concentration is still within the target uncertainty at an ambient pressure of approximately 500 hPa.
Quantitative chemical analysis of airborne particulate matter (PM) is vital for the understanding of health effects in indoor and outdoor environments, as well as for enforcing EU air quality regulations. Typically, airborne particles are sampled over long time periods on filters, followed by lab-based analysis, e.g., with inductively coupled plasma mass spectrometry (ICP-MS). During the EURAMET EMPIR AEROMET project, cascade impactor aerosol sampling is combined for the first time with on-site total reflection X-ray fluorescence (TXRF) spectroscopy to develop a tool for quantifying particle element compositions within short time intervals and even on-site. This makes variations of aerosol chemistry observable with time resolution only a few hours and with good size resolution in the PM10 range. The study investigates the proof of principles of this methodological approach. Acrylic discs and silicon wafers are shown to be suitable impactor carriers with sufficiently smooth and clean surfaces, and a non-destructive elemental mass concentration measurement with a lower limit of detection around 10 pg/m3 could be achieved. We demonstrate the traceability of field TXRF measurements to a radiometrically calibrated TXRF reference, and the results from both analytical methods correspond satisfactorily.
A new facility has been developed which allows for a stable and reproducible production of ambient-like model aerosols (PALMA) in the laboratory. The set-up consists of multiple aerosol generators, a custom-made flow tube homogeniser, isokinetic sampling probes, and a system to control aerosol temperature and humidity. Model aerosols containing elemental carbon, secondary organic matter from the ozonolysis of α-pinene, inorganic salts such as ammonium sulfate and ammonium nitrate, mineral dust particles,and water were generated under different environmental conditions and at different number and mass concentrations. The aerosol physical and chemical properties were characterised with an array of experimental methods, including scanning mobility particle sizing, ion chromatography, total reflection X-ray fluorescence spectroscopy and thermo-optical analysis. The facility is very versatile and can find applications in the calibration and performance characterisation of aerosol instruments monitoring ambient air. In this study, we performed, as proof of concept, an intercomparison of three different commercial PM (particulate matter) monitors (TEOM1405, DustTrak DRX 8533 and Fidas Frog) with the gravimetric reference method under three simulated environmental scenarios. The results are presented and compared to previous field studies. We believe that the laboratory-based method for simulating ambient aerosols presented here could provide in the future a useful alternative to time-consuming and expensive field campaigns, which are often required for instrument certification and calibration.
Die im Rahmen dieser Arbeit vornehmlich untersuchten supermartensitischen Stähle werden im Offshore-Bereich als geschweißte Flowlines eingesetzt. Diese Stähle sollen nach dem Prinzip „Fitness for Purpose“ bisher verwendete höher legierte Werkstoffe ersetzen. Die neuen Stähle sind aufgrund ihrer Korrosionsbeständigkeit und Festigkeit sehr gut für das beabsichtigte Einsatzgebiet geeignet. Im Sour Service besteht jedoch die Gefahr der Wasserstoffaufnahme mit nachfolgender Rissbildung. Zur Beurteilung der Risssicherheit der Schweißverbindungen sowie des unbeeinflussten Werkstoffes im Anlieferungszustand werden Wasserstofftransportdaten benötigt. Diese werden im Rahmen dieser Arbeit mittels Permeationsexperimenten an Stahlmembranen unter realistischen Einsatzbedingungen quantifiziert, so dass die Ergebnisse in computergestützte Lebensdauerberechnungen Eingang finden können. Die Untersuchungen zeigten, dass der Diffusionskoeffizient des jeweiligen Werkstoffs bzw. Gefüges nicht von der chemischen Zusammensetzung der Prüflösung abhängt. Die Subsurface-Konzentration, das ist die in die Werkstoffe eintretende Wasserstoff- konzentration, hängt dagegen vom pH-Wert, von der Schwefelwasserstoffsättigung und von der Zusammensetzung der Prüflösung ab. Die Abhängigkeit der Subsurface-Konzentration von der chemischen Zusammensetzung der Prüflösung wird zudem entscheidend durch die Chloridionenkonzentration bestimmt. Darüber hinaus wurde festgestellt, dass die chemische Zusammensetzung supermartensitischer Stähle das Permeationsverhalten erheblich beeinflusst. Beim Vergleich des Permeationsverhaltens von wärmebehandelten Proben mit Proben realer Schweißnahtgefüge ergaben sich Differenzen in Höhe einer Größenordnung. Das bedeutet letztlich, dass das Permeationsverhalten von Wasserstoff in solchen Schweiß- verbindungen für jeden Fall, abhängig von der chemischen Zusammensetzung und Temperaturführung, separat zu untersuchen ist. Zusätzlich wurde die Wasserstoffdiffusion und -aufnahme in Schweißnahtgefügen höchstfester Feinkornbaustähle untersucht. Die Ergebnisse zeigten, dass diese Werkstoffe schon bei geringfügig abgesenkten pH-Werten, wie sie in Spalten oder Rissen aufgrund von Hydrolyse vorherrschen können, Wasserstoff aufnahmen. Die Subsurface-Konzentration war wiederum von der chemischen Zusammensetzung der Prüfelektrolytlösung abhängig. Generell waren die Diffusionskoeffizienten und die Subsurface-Konzentrationen stark vom Gefüge abhängig. Der Vergleich der Resultate der höchstfesten Feinkornbaustähle S 1100 und S 890 zeigte, dass die Wasserstoffpermeation bei diesen Werkstofftypen weniger große Unterschiede aufwies als bei den supermartensitischen Stählen.
Fiber optic sensors based on polymer optical fibers (POF) have the advantage of being very elastic and robust at the same time. Unlike silica fibers, standard PMMA POF fibers can be strained to more than 40% while fully maintaining their light guiding properties. We investigated POF as a distributed strain sensor by analysing the backscatter increase at the strained section using the optical time domain reflectometry (OTDR) technique. This sensing ability together with its high robustness and break-down strain makes POF well-suited for integration into technical textiles for structural health monitoring purposes. Within the European research project POLYTECT (Polyfunctional textiles against natural hazards) technical textiles with integrated POF sensors, among others sensors are being developed for online structural health monitoring of geotechnical structures. Mechanical deformation in slopes, dams, dikes, embankments and retrofitted masonry structures is to be detected before critical damage occurs. In this paper we present the POF strain sensor properties, reactions to disturbing influences as temperature and bends as well as the results of the different model tests we conducted within POLYTECT. We further show the potential of perfluorinated graded-index POF for distributed strain sensing with increased spatial resolution and measurement lengths.
This article reports a comprehensive investigation of the average and local structure of La5.6WO12-δ, which has excellent mixed proton, electron and oxide ion conduction suitable for device applications. Synchrotron X-ray and neutron powder diffraction show that a cubic fluorite supercell describes the average structure, with highly disordered lanthanum and oxide positions. On average, the tungsten sites are sixfold coordinated and a trace [3.7 (1.3)%] of anti-site disorder is detected. In addition to sharp Bragg reflections, strong diffuse neutron scattering is observed, which hints at short-range order. Plausible local configurations are considered and it is shown that the defect chemistry implies a simple 'chemical exchange' interaction that favours ordered WO6 octahedra. The local model is confirmed by synchrotron X-ray pair distribution function analysis and EXAFS experiments performed at the La K and W L-3 edges. It is shown that ordered domains of similar to 3.5 nm are found, implying that mixed conduction in La5.6WO12-δ is associated with a defective glassy-like anion sublattice. The origins of this ground state are proposed to lie in the nonbipartite nature of the face-centred cubic lattice and the pairwise interactions which link the orientation of neighbouring octahedral WO6 sites. This 'function through frustration' could provide a means of designing new mixed conductors.
Polymer optical fiber (POF) sensors have the unique ability to measure high strain distributed along the fiber up to 40% using the optical time-domain reflectometry (OTDR) technique. Both, standard PMMA fibers and perfluorinated (PF) graded-index (GI) POF are introduced and evaluated in potential use and applicability. Further, distributed length change measurement based on cross-correlation analysis of the characteristic fiber signature of PF POF is introduced. We conclude the advances in distributed POF strain sensors technology with respect to application in structural health monitoring. Special focus is on the sensor integration into technical textiles for health monitoring of geotechnical structures and masonry structures. Measurement results of sensor-equipped textiles in different model tests are presented, displacement of soil and cracks in retrofitted masonry structures are detected and evaluated.
In this work, we characterise the performance of a Sharp optical aerosol sensor model GP2Y1010AU0F. The sensor was exposed to different environments: to a clean room, to a controlled atmosphere with known aerosol size distribution and to the ambient atmosphere on a busy city street. During the exposure, the output waveforms of the sensor pulses were digitised, saved and a following offline analysis enabled us to study the behaviour of the sensor pulse-by-pulse. A linear response of the sensor on number concentration of the monosized dispersed PSL particles was shown together with an almost linear dependence on particle diameters in the 0.4 to 4 micrometer range.
The gathered data about the sensor were used to predict its response to an ambient atmosphere, which was observed simultaneously with a calibrated optical particle counter.
Mixed ionic electronic conducting ceramics Nd6-yWO12-d (d is the Oxygen deficiency) provide excellent stability in harsh environments containing strongly reactive gases such as CO2, CO, H2, H2O or H2S. Due to this chemical stability, they are promising and cost-efficient candidate materials for gas separation, catalytic membrane reactors and protonic ceramic fuel cell technologies. As in La6-yWO12-d, the ionic/electronic transport mechanism in Nd6-yWO12-d is expected to be largely controlled by the crystal structure, the conclusive determination of which is still lacking. This work presents a crystallographic study of Nd5.8WO12-d and molybdenum-substituted Nd5.7W0.75Mo0.25O12-d prepared by the citrate complexation route. High-resolution synchrotron and neutron powder diffraction data were used in combined Rietveld refinements to unravel the crystal structure of Nd5.8WO12-d and Nd5.7W0.75Mo0.25O12-d. Both investigated samples crystallize in a defect fluorite crystal structure with space group Fm3m and doubled unit-cell parameter due to cation ordering. Mo replacesWat bothWyckoff sites 4a and 48h and is evenly distributed, in contrast with La6-yWO12-d. X-ray absorption spectroscopy as a function of partial pressure pO2 in the near-edge regions excludes oxidation state changes of Nd (Nd3+) and W(W6+) in reducing conditions: the enhanced hydrogen permeation, i.e. ambipolar conduction, observed in Mo-substituted Nd6-yWO12-d is therefore explained by the higher Mo reducibility and the creation of additional – disordered – oxygen vacancies.
Ultrafine particles emitted from laser printers are suspected to elicit adverse health effects. We performed 75-minute exposures to emissions of laser printing devices (LPDs) in a standardized, randomized, cross- over manner in 23 healthy subjects, 14 mild, stable asthmatics, and 15 persons reporting symptoms associated with LPD emissions. Low-level exposures (LLE) ranged at the particle background (3000 cm−3) and High-level exposures (HLE) at 100 000 cm−3. Examinations before and after exp sures included spirometry, body plethysmography, transfer factors for CO and NO (TLCO, TLNO), bronchial and alveolar NO, cytokines in serum and nasal secretions (IL-1β, IL-5, IL-6, IL-8, GM-CSF, IFNγ, TNFα), serum ECP, and IgE. Across all participants, no statistically significant changes occurred for lung mechanics and NO. There was a decrease in volume-related TLNO that was more pronounced in HLE, but the difference to LLE was not significant. ECP and IgE increased in the same way after exposures. Nasal IL-6 showed a higher increase after LLE. There was no coherent pattern regarding the responses in the participant subgroups or single sets of variables. In conclusion, the experimental acute responses to short but very high-level LPD exposures were small and did not indicate clinically relevant effects compared to low particle number concentrations.