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This work presents results of investigations towards the emission of chemical reaction products and sound pressure during an outdoor and an indoor firework display. Potentially harmful and toxic gases, and aerosols, were measured as well as sound pressures. Aerosols were measured with a Differential Mobility Analyzer (DMA) as well as a Laser Particle Counter. The focus was on particles with diameters between 11 nm and 20 µm. A transportable Fourier Transform Infrared (FTIR) spectroscopy detector registered the concentrations of emitted reaction gases, simultaneously. During the outdoor firework display, peak particle concentrations of >550000 particles cm-3, equivalent to a mass concentration of approximately 3.95 mg m-3, were detected, revealing a concentration maximum at approximately 175 nm particle diameter. The time-averaged particle mass concentration did not exceed 1.58 mg m-3 over 15 minutes. Due to the large distances (110 m) to the firing points, no significant harmful or toxic gas concentrations were measured during the entire firework display. In contrast, concentrations of sulphur dioxide (SO2) rose after an indoor firework display in a large event hall. On two days, more than 23000 particles cm-3 (which equates to a mass concentration of approximately 0.41 mg m-3) were detected when the hall ventilation was turned off, and more than 11000 particles cm-3 (which equates to a mass concentration of approximately 1.18 mg m-3) when the hall ventilation was activated. Concentration maxima appeared at approximately 300 nm particle diameter. The time-averaged particle concentrations in this case did not exceed 0.56 mg m-3 (over 15 minutes).
Berichtet wird über ein abgeschlossenes Folgeprojekt zu vorangegangenen Forschungsprojekte zum gleichen Thema. In diesem Projekt wurde das Messverfahren und der Prüfwert für die Partikelemission aus Bürogeräten (siehe Vergabegrundlage DE-UZ 205, Anhang S-M) validiert und weiterentwickelt. Dies geschah erstens durch Auswertung der Qualität der im Zuge der Antragsbearbeitung für das Umweltzeichen beim RAL vorgelegten Prüfberichte der zugelassenen Prüfinstitute und - basierend darauf - durch Erarbeitung von technisch-methodischen Veränderungsvorschlägen für die Prüfung der chemischen Emissionen, inklusive der Partikelemissionen. Zweitens wurde zur Beurteilung der Veränderung der Emissionen aktueller gegenüber älteren Geräte-generationen ein nicht repräsentativer Pool von table-top-Laserdruckern aufgebaut und die chemischen Emissionen wurden gemäß DE-UZ-205, Anhang S-M gemessen. Ergänzend wurde eine quantitative chemische Analyse der anorganischen Feststoffe - insbesondere der Metalle - in den emittierten Aerosolen vorgenommen die Feststoffgehalte um 2 Massen-% ergaben. Diese Ergebnisse wurden gemeinsam mit neueren wissenschaftlichen Untersuchungen zur gesundheitlichen Bewertung der Emissionen aus Laserdruckern ausgewertet, es besteht kein Handlungsbedarf hinsichtlich einer Veränderung von Prüfkriterien und Prüfwerten. Drittens wurde untersucht und bestätigt, dass mit dem Ziel eines zukünftigen Umweltzeichens das Emissionsverhalten Kunststoff verarbeitender 3D-FDM-Drucker und/oder die darin verarbeiteten Verbrauchsmaterialien (Filamente) mit dem für Laserdrucker entwickelten Mess- und Prüfschema charakterisiert und quantifiziert werden können. Untersuchungen an Stereo-lithografie (SLA)-Druckern und Vorrichtungen zur Nach-Aushärtung (Curing Units) ergaben keine nachweisbaren Partikelemissionen.
Beim Abbrand einzelner Feuerwerkskörper für den Indoor-Bereich wurden als gasförmige Hauptreaktionsprodukte unter anderem CO2, CO, COS, nitrose Gase, diverse Kohlenwasserstoffe und Schwefelverbindungen (teilweise in sehr hohen Konzentrationen) mit Hilfe der FTIR-Spektroskopie nachgewiesen. Zusätzliche Feinstaubmessungen parallel zum Abbrand in einem großen Raum illustrierten die zeitweise hohen Partikelkonzentrationen an unterschiedlichen Messpunkten.
Partikelemissionen aus Laserdruckern sind seit längerem bekannt und wurden bislang als Feinstaubmasse bei der Prüfwertvergabe für den Blauen Engel begrenzt. Seit einigen Jahren weiß man, dass neben den Feinstaubpartikeln auch ultrafeine Partikel beim Betrieb von Laserdruckern emittiert werden. Diese Emissionen lassen sich nur eingeschränkt bis gar nicht über Nachrüstfilter am Druckgerät minimieren. Das Umweltbundesamt (UBA) hat dies zum Anlass genommen, die Prüfvorgaben für den Blauen Engel im Hinblick auf die Erfassung ultrafeiner Partikel anzupassen und zu verschärfen. UBA hat hierzu einen Forschungsauftrag an die Bundesanstalt für Materialforschung und -prüfung (BAM) vergeben. Testverfahren und Prüfvorgaben sind nunmehr erarbeitet und werden im Beitrag vorgestellt. Die geänderten Prüfbedingungen sollen ab 2013 in die Prüfvorgabe eingeführt werden. Etwa drei Viertel der derzeit am Markt erhältlichen Laserdrucker werden die strengen Prüfvorgaben nicht erfüllen können.
Konzepte zur ISO-Kalibrierung der Messung von Partikelgrößen und Partikelanzahlkonzentrationen
(2012)
Long term waste containment - A challenge to geotextiles and geomembranes made of plastic materials
(1997)
Geomembranes used in basal liner systems of landfills must not be damaged by the coarse gravel of the standard drainage layer. Therefore, the geomembrane must be protected against mechanical damage and strain by means of a suitable protective layer. The main requirements for this protective layer as well as the long-term durability of the mineral and geotextile components are compiled in the guideline recently released by German authorities. An overview is given on the existing types of protective layer systems with the state-of-the-art testing, the requirements and selected results of related research programs.
Dr. Stefan Seeger of the German Federal Institute for Materials Research and Testing (Bundesanstalt für Materialforschung und -prüfung - BAM) tells of his successful experience using Granta's CES software to make an eco-materials knowledge resource for automotive, construction, and other industries in the Berlin region.
Zulassung von Schutzlagen
(1995)
Untersuchung der Wirksamkeit von Filtern zum Schutz vor Partikelemissionen aus Laserdrucksystemen
(2012)
Laserdrucksysteme (Laserdrucker, -kopierer, Multifunktionsgeräte) emittieren in sehr unterschiedlichen Mengen Partikel im Größenbereich zwischen 5 und 300 nm, die im Druckbetrieb überwiegend durch Kondensation aus der Gasphase entstehen. Eine präventive Minderung dieser Emissionen ist sinnvoll. Die Filtration der in Laserdruckern entstehenden Aerosole bietet eine Option für eine wirksame Emissionsminderung. Die untersuchten Filter mit verschiedenen Filterkonzepten zeigten in ihrer Wirkung deutliche Unterschiede. Die Ergebnisse unterstreichen die Notwendigkeit der gerätespezifischen Optimierung von Filtern für die Anwendung in Laserdrucksystemen.----------------------------------------------------------------------------------------------------------------------------------------------
Laser printing devices are sources of particle emission in different quantities in the size range between 5 and 300 nm. The particles are predominantly generated by re-condensation from the gas phase. Emission mitigation as a precautionary measure should be considered and exhaust air filtration is one technical option. Two particle filters with different filter concepts were compared and revealed different levels of performance. The result underpins the need for individual filter solutions for laser printing devices.
Partikelanalyse im Brandfall
(2013)
Geosynthetic clay liners (GCLs) often have a sandwich-like multilayer structure, e.g. bentonite encased between two geotextile layers connected by fibers or yarns, either by needle-punching or stitch-bonding. Therefore, the internal shear strength of the GCL depends on the strength of reinforcing fiber bundles or yarns and their anchoring strength in the cover and carrier geotextiles. When used on long and steep slopes and covered with thick soil layers, the GCL is permanently exposed to a combined action of compressive and shear stress. Such load conditions are characteristic for landfill covers and the slope stability of the overall cover system in the long run strongly depends on the long-term internal shear strength of the GCL. A new test method was developed to study this long-term shear behavior. The focus was not only on creep, as it is normally done, but on aging effects. The shear test devices allow the measurement of creep curves and times-to-failure at elevated temperatures in different media (tap water and de-ionized water). In this publication, the main findings of the experiments on needle-punched GCLs with and without thermal treatment are summarized. Tap water as a test medium was essential to ensure sodium to calcium ion exchange in the bentonite layer. Under this condition extremely long test durations without failure were achieved. Sliding failure occurred when de-ionized water was used. Two failure modes were observed: brittle failure of the GCLs with thermal treatment and slow disentanglement of fiber bundles for untreated GCLs. Short-term shear strength (e.g. peel strength) is unrelated to the actual long-term shear strength, i.e. to the times-to-failure achieved in long-term shear strength test. Hence, short-term shear strength alone will not provide reliable dimensioning data for product design and choice of resins. Therefore, the often suggested approach, namely, restriction to short-term tests only and application of factors of safety, is challenged by these results.
A screening test for potential emissions of volatile organic compounds (VOC) was run on different thermoplastic filaments used for 3D printing. The method of direct thermal desorption was used to simulate the high temperatures during the 3D printing process and to identify the main compounds emitted from the filaments. A )arge number of unexpected compounds were detected that might affect the user's health and have an impact on indoor air chemistry.
Measurements of aerosol particles are vital for enforcing EU air quality regulations to protect human health, and for research on climate change effects. Although metrics such as PM10 and PM2.5 are currently in use, the level of uncertainty of aerosol metrics is too high and the traceability is insufficient. The project AEROMET, which has been started in June 2017 aims at implementing improvements in a) the uncertainty of particle mass, size and number concentration measurements and b) in the characterization of regulated components in airborne particles. Both are demanded by existing networks within the EU as well as by global atmospheric research.
On-site measurement campaigns
One of the objects is the application of mobile x-ray spectroscopy techniques combined with aerosol sampling techniques for quantifying particle compositions in the field for real time analysis. During two in-field measurement campaigns in Budapest, Hungary in May 2018 and Cassino, Italy in September 2018 the size dependent mass concentrations of specific elements in ambient aerosols were monitored under dynamic conditions.
Typically, airborne particles are sampled on filter substrates. During this project new sampling methods with specially designed substrate holders for an in-situ TXRF analysis were developed and applied for the first time. This approach allows a direct time and size resolved analysis without laborious digestion steps and a reduced risk of contamination.
Aerosol particles were sampled in a 13-stage DLPI impactor - size range from 0,03 µm to 10 µm - which was equipped with special adapters for acrylic discs of 30 mm diameter, serving as substrates. TXRF analysis was performed on site with the transportable spectrometer S2 PICOFOX (Bruker Nano GmbH) equipped with a Mo X-ray tube and a 30 mm² Silicon Drift Detector (SDD). Excitation conditions were 50 kV, 600 µA, measurement time 1000 s. Quantification was based on internal standardization using 50 ng of Y in solution, which was pipetted into the centre of the discs prior to sampling.
At moderate air pollution levels, i.e. PM10 ~ 20 µg/m³, sampling times of less than 2 hours were enough for the detection of elements in different particle size bins. The in-situ approach and the high sensitivity of TXRF enables the observation of rather quick changes in the quantity and distribution of elements in an ambient aerosol on the day of sampling, as the below example from the Cassino field campaign on 11 Sept. 2018 shows: The analysis of the morning and afternoon sampling shifts reveals the occurrence of the elements Fe, Ca and Si in different size bins as well as their significant temporal change in respective mass concentrations over the day while the distributions of several other elements in the aerosol remain unchanged.
The validation of these results by backup measurements is planned.
A mobile Bruker S2 Picofox TXRF spectrometer has been used in two field campaigns within the EMPIR env07 AEROMET project for the on-site analysis of cascade impactor aerosol samples.The results show that even at moderate air pollution levels – i.e.PM10 fairly below 20 μg/m³ - element mass concentrations in air in the range of 100 pg/m³could be measured in up to 13 size bins after sampling times of less than only 0.5 days.
The physical and chemical analysis of aerosols using reliable and physically traceable methods is important for the thorough investigation of airborne particles to support a better understanding of their origin as well as their health and climate impacts. Within the European Metrology Research AeroMet project,the aim of hysikalisch–Technische Bundesanstalt’s (PTB) X-ray spectrometry group is to develop and establish traceable and reliable X-ray methods to measure the elemental mass deposition per unit area, the elemental composition,and the chemical binding state of particulate matter supported by a flat substrate. This approach can substantially contribute to support quantitative analytical methods during on-site measurement campaigns where portable Instrumentation is employed by qualifying suitable calibration samples for commercial analytical X-ray instruments and by investigating samples collected during the field campaign.
3D-printing or additive manufacturing has many promising and unique advantages. Especially low cost molten polymer Deposition Printers are increasingly populär in the private and educational sector.
Their environmental friendliness can be questioned due to recently reported ultrafine particle and suspected VOC emissions, To further investigate 3D-printing as a potential indoor air pollution source we characterized fine and ultrafine particle emissions from a molten polymer deposition printer producing a 3D object with ten marketable polymer filament materials under controlled conditions in a test chamber. VOC emissions from the filaments have also been compared. Using a straightforward emission model time dependent and averaged particle emission rates were determined. The results indicate that under comparable conditions some filament materials produce mainly ultrafine particles up to an average rate of 1013 per minute. This value is in the upper ränge of typical indoor ultrafine particle sources (e.g. Smoking, frying, candle light, laser printer). The observed material-specific rates differ by five Orders of magnitude. Filament-specific gaseous emissions of organic compounds such as bisphenol A, styrene and others were also detected.
Our results suggest a detailed evaluation of related risks and considering protective measures such as housing and filtering.