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In this work, the elemental composition of fine and ultrafine particles emitted by ten different laser printing devices (LPD) is examined. The particle number concentration time series was measured as well as the particle size distributions. In parallel, emitted particles were size-selectively sampled with a cascade impactor and subsequently analyzed by the means of XRF. In order to identify potential sources for the aerosol's elemental composition, materials involved in the printing process such as toner, paper, and structural components of the printer were also analyzed. While the majority of particle emissions from laser printers are known to consist of recondensated semi volatile organic compounds, elemental analysis identifies Si, S, Cl, Ca, Ti, Cr, and Fe as well as traces of Ni and Zn in different size fractions of the aerosols. These elements can mainly be assigned to contributions from toner and paper. The detection of elements that are likely to be present in inorganic compounds is in good agreement with the measurement of nonvolatile particles. Quantitative measurements of solid particles at 400 °C resulted in residues of 1.6 × 109 and 1.5 × 1010 particles per print job, representing fractions of 0.2% and 1.9% of the total number of emitted particles at room temperature. In combination with the XRF results it is concluded that solid inorganic particles contribute to LPD emissions in measurable quantities. Furthermore, for the first time Br was detected in significant concentrations in the aerosol emitted from two LPD. The analysis of several possible sources identified the plastic housings of the fuser units as main sources due to substantial Br concentrations related to brominated flame retardants.
Several construction and building materials, including wood, glue and coatings, are possible sources of very volatile organic compounds (VVOCs) and volatile organic compounds (VOCs) like formic and acetic acid. Due to very high air tightness and very low air exchange rates in new buildings concentrations of these harmful substances can increase considerably. To minimize the risk, emissions from building products should be identified and quantified. With the common standard method, this means Tenax® sampling followed by thermal desorption and GC-MS analysis, these acids could not be detected sufficiently. The aim oft this study is the comparison of two different methods for the determination of acetic and formic acid. The sampling of method one, which is usually used for identification and quantification of VOCs, is done in accordance with ISO 16000-6 and ISO 16017-1 on Carbotrap® 202 multi-bed thermal desorption tube by subsequent identification and quantification with GC-MS. Method two is based on sampling on 2,4-dinitrophenylhydrazine (DNPH) cartridges, derivatisation, elution, identification and quantification of the derivatives with LC-MS/MS (liquid chromatography mass spectrometry/mass spectrometry).
Methods for the determination of biocide emissions from treated materials into water and air were developed and tested in order to support a comparative ecological assessment of biocidal products. Leaching tests, experiments with simulated rain, extraction cleaning of carpets and emission chamber tests were performed with a series of treated materials. The experiments focused on the effect of changes in the procedure as well as characteristics of the specimens and demonstrate the suitability of the proposed methods for biocides of different product types.
It was demonstrated that emissions of biocides into water can be compared on the basis of leaching tests in which the emission kinetics of the active ingredients are recorded. However, the water volume per surface area and the timetable for water changes have to be defined in such tests. Functions of flux rates related to time can be well described for inorganic compounds, whereas modelling of the data is more complicated for organic substances.
Emission chamber tests using 20-litre and 23-litre glass exsiccators, originally developed to study volatile organic compounds, were successfully adapted for the investigation of the emission of biocides from treated materials which are usually semi volatile organic compounds. However, test parameters and the method of analysis have to be adapted to the substances to be determined.
Generally, it was found that the emission curves for the semi volatile organic compounds investigated differ from those of volatile organic compounds.
Background to the studies was the revision of the current selection criteria of the German ecolabel Blauer Engel (Blue angel) for copiers and printers. In the requirements limits were set for ozone, dust and styrene emissions. The former test methods did no longer correspond to todays requirements with regard to emission measurements. In addition, the emission behaviour of hardcopy devices due to the use of different and non-com parable test methods has been recently discussed controversely. For this reason a new test method had to be developed which enables a reliable, reproducible determination of emission rates (ER) for dust, ozone and VOC (volatile organic compounds). The basis for this was the ECMA-Standard 328 compiled by ECMA (European Computer Manufacturer Association) using dynamic chamber measurements. Nine different machines, desktop laser printers as well as office devices like bigger copiers and multifunctional devices were investigated. As a result of the study new criteria for the Blauer Engel for copiers, printers and a new created for multifunctional devices, concerning TVOC, ozone and dust emission were determined. Additionally a model is presented calculating the concentrations in real rooms under usual printing conditions derived from the test chamber results.
The development of a gas mixing system (GMS) that enables dynamic and retraceable production of stable long-term VOC gas mixtures within the ppb range is discussed. In this system pure liquid substances are kept separately at a constant temperature, evaporated according to their vapour pressure and removed by a small inert gas flow. A modular set-up allows flexible handling. All vapours generated are finally united in a mixing chamber. Any concentration level of the gas mixture can be produced by a suitable combination of evaporation temperature, carrier and dilution gas flows. Test results from continuous operation over six weeks are presented. The equipment was tested on seven volatile organic compounds (VOC) of different vapour pressure ranges. It was possible to establish stable operation for the equipment during the entire period and reproducible gas concentrations which were traceable to the mass as an SI unit, thus the system is suitable for long-term tests.---------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------
Im Beitrag wird die Entwicklung eines Gasmischsystems (GMS) beschrieben, das die dynamische und rückführbare Generierung von langzeitstabilen VOC-Gasgemischen im ppb-Bereich erlaubt. Dabei werden Reinsubstanzen separat temperiert, ihrem Dampfdruck entsprechend verdampft und durch einen kleinen Inertgasstrom abgeführt. In einer Mischkammer werden sie schließlich zusammengeführt. Durch die Kombination von Verdampfungstemperatur, Träger- und Verdünnungsgasflüssen ist die Einstellung eines beliebigen Konzentrationsniveaus des Gasgemischs möglich. Aus einem Dauerbetrieb von sechs Wochen werden Untersuchungsergebnisse gezeigt. Dabei wurde die Apparatur mit insgesamt sieben flüchtigen organischen Verbindungen (VOC) unterschiedlicher Dampfdruckbereiche betrieben. Die Anlage lief über den gesamten Zeitraum stabil und lieferte reproduzierbare und auf die Masse als SI-Einheit rückführbare Gaskonzentrationen. Somit ist das Verfahren für Langzeitanwendungen geeignet.
When utilized in the perfuming of children's toys, fragrances capable of inducing contact allergy in human skin may also become bioavailable to children via the inhalation route. The aim of this study was to determine the area-specific emission rates of 24 fragrances from a plasticized PVC reference material that was meant to mimic a real plastic toy. This material was introduced into an emission chamber for 28 days at handling conditions or at worst-case conditions. As a result, fragrances can be separated into three categories according to their emission rates ranging from 0.0041 to 16.2 mg/m² × h, i.e., highly volatile, semivolatile, and low-volatile compounds. Compounds of the first and second categories were monitored with decreasing emission rates. Substances of the third category were detected with increasing emission rates over time. Further, higher temperatures led to higher emission rates. The emission concentration of fragrances from four real scented toys varied between 1.10 and 107 µg/m³ at day 1 in the test chamber. Therefore, short-term inhalation exposure to fragrances originating from toys was in the range of 0.53–2700 ng/kg BW/d for the children of age 1 and older. Long-term exposure to these fragrances was calculated in the range of 2.2–220 ng/kg BW/d.
Vor dem Hintergrund der notwendigen Revision der Kriterien zur Vergabe des Gütezeichens "Blauer Engel" für Laserdrucker, Kopierer und Multifunktionsgeräte mussten auch die Prüfmethoden angepasst werden, da die alten Verfahren nicht mehr die heutigen Anforderungen der Emissionsmessung erfüllen. In diesem Zusammenhang wurde auch das unterschiedliche Emissionsverhalten von Hardcopy-Geräten auf Grund der verschiedenen und nicht miteinander vergleichbaren Prüfverfahren heftig diskutiert. Aus diesen Gründen wurde ein neues Prüfverfahren entwickelt, mit dem eine verlässliche und reproduzierbare Prüfung der Emissionsraten von Staub, Ozon und flüchtiger organischer Verbindungen auf der Basis des ECMA (European Computer Manufacturer Association) Standards 328 möglich ist. Dazu wurden neun verschiedene Geräte unter verschiedenen Bedingungen untersucht. Als ein Ergebnis dieser Studie wurden neue Kriterien zur Vergabe des "Blauen Engels" für Kopierer, Drucker und Multifunktionsgeräte festgelegt.
Die Analytik von Phthalaten (DMP bis DEHP) in der Luft ist mit thermischer Desorption unter Verwendung von Quarzwolle als Adsorbens erfolgreich realisierbar. Dies wurde durch eine Methodenvalidierung bestätigt. Es wurden sowohl Messungen im Innenraum als auch in Emissionskammern vorgenommen. In den Emissionskammermessungen wurden mögliche Senkeneffekte der Kammeroberfläche (Glas) untersucht. Unter Zuhilfenahme der idealen Abklingkurve wird bestätigt, dass diese Oberfläche eine Senke darstellt.