Sanitär- und Kommunaltechnik; Umwelttechnik
Filtern
Erscheinungsjahr
Dokumenttyp
- Vortrag (834)
- Zeitschriftenartikel (613)
- Posterpräsentation (356)
- Beitrag zu einem Tagungsband (201)
- Forschungsbericht (28)
- Sonstiges (27)
- Zeitschriftenheft (Herausgeberschaft für das komplette Heft) (27)
- Buchkapitel (25)
- Dissertation (13)
- Beitrag zu einem Sammelband (9)
Sprache
- Englisch (1530)
- Deutsch (603)
- Mehrsprachig (10)
- Französisch (3)
- Polnisch (2)
Schlagworte
- Fluorescence (58)
- Mikroplastik (58)
- Microplastics (57)
- Corrosion (51)
- Biocides (48)
- Recycling (47)
- Immunoassay (46)
- Leaching (46)
- Soil (37)
- Antimicrobial resistance (35)
Organisationseinheit der BAM
- 4 Material und Umwelt (756)
- 1 Analytische Chemie; Referenzmaterialien (321)
- 4.1 Biologische Materialschädigung und Referenzorganismen (194)
- 4.3 Schadstofftransfer und Umwelttechnologien (194)
- 6 Materialchemie (186)
- 4.4 Thermochemische Reststoffbehandlung und Wertstoffrückgewinnung (168)
- 7 Bauwerkssicherheit (159)
- 1.8 Umweltanalytik (127)
- 6.6 Physik und chemische Analytik der Polymere (118)
- 4.0 Abteilungsleitung und andere (116)
Paper des Monats
- ja (22)
Rising temperatures worldwide pose an increasing challenge for safe and healthy living conditions. Particularly inner cities have been affected by these environmental changes because of the materials used to build houses, streets and infrastructure. The most common building material is concrete. It shows a specific heat capacity, while the heat conductivity for Standard concrete is low. Thus, the use of concrete generates a high capacity of heat storage. In addition, extensive soil sealing also contributes to the temperature rise of inner city areas compared to
their surroundings. To mitigate this so-called urban heat island effect, a self-cooling concrete paver was developed. This paver is able to store water. The evaporation of the water at elevated temperatures provides a cooling effect. This paper focuses on determination of this new paver’s capability to cool the surface and the surrounding. The new paver’s cooling Qualities were analysed in a series of laboratory tests. To prove the results outside of laboratory conditions, two fields (12 m × 8 m) with self-cooling and reference pavers were installed in Spain.
This paper presents and discusses the results of the tests. Correlation between reduced surface temperature of the self-cooling concrete pavers and the air temperature is examined.
Afin de garantir la qualité des eaux en Europe, la Commission Européenne a demandé aux États Membres, de leur fournir des résultats de mesure comparables et traçables pour l’analyse des polluants critiques. Devant ces enjeux considérables pour la protection de l’environnement, l’apport de la métrologie est nécessaire pour améliorer la fiabilité des analyses et permettre la comparabilité des résultats. C’est pourquoi, le projet de recherche européen Euramet/EMRP/ENV08 « Traçabilité des mesures pour la surveillance des polluants critiques de la DCE, Directive Cadre européenne sur l’Eau (2000/60/CE) », financé par l’EMRP, avait pour objectif de fournir des éléments pour la mise en place d’une base métrologique. Des méthodes de référence primaires permettant d’analyser des substances dangereuses prioritaires y sont développées pour répondre aux exigences de la DCE en termes de niveaux de performance (limites de quantification et incertitudes). Les hydrocarbures aromatiques polycycliques (HAP), substances dangereuses prioritaires « orphelines » de méthodes DCE compatibles, font partie des polluants ciblés par le projet. Le développement et la validation de la méthode d’analyse des HAP dans l’eau totale ont été réalisés. La méthode qui satisfait au mieux les exigences de la DCE en termes de concentrations et d’incertitudes accessibles est l’extraction en phase solide (SPE) sur un support disque suivie d’une analyse par dilution isotopique associée à la chromatographie en phase gazeuse couplée à la spectroscopie de masse (DI-CG/SM).
The European Water Framework Directive 2000/60/EC requires monitoring of organic priority pollutants in so-called whole water samples, i.e. in aqueous nonfiltered samples that contain natural colloidal and suspended particulate matter. Colloids and suspended particles in the liquid phase constitute a challenge for sample homogeneity and stability. Within the joint research project ENV08 ‘‘Traceable measurements for monitoring critical pollutants under the European Water Framework Directive 2000/60/EC’’, whole water test materials were developed by spiking defined amounts of aqueous slurries of ultrafinely milled contaminated soil or sediment and aqueous solutions of humic acid into a natural mineral water matrix. This paper presents the results of an European-wide interlaboratory comparison (ILC) using this type of test materials. Target analytes were tributyltin, polybrominated diphenyl ethers and polycyclic aromatic hydrocarbons in the ng/L concentration range. Results of the ILC indicate that the produced materials are sufficiently homogeneous and stable to serve as samples for, e.g. proficiency testing or method validation. To our knowledge, this is the first time that ready-to-use water materials with a defined amount of suspended particulate and colloidal matter have been applied as test samples in an interlaboratory exercise. These samples meet the requirements of the European Water Framework Directive. Previous proficiency testing schemes mainly employed filtered water samples fortified with a spike of the target analyte in a water-miscible organic solvent.
We have prepared and evaluated three whole water test materials containing eight polycyclic aromatic hydrocarbons (PAHs), six polybrominated diphenyl ethers (PBDEs) and tributyltin (TBT) with respect to homogeneity and short-term stability. The test materials were used as samples in two inter-laboratory comparisons. The materials were composed of natural mineral water and model suspended particulate matter (SPM) containing the target compounds at ng L-1 levels. The expanded uncertainty of the estimated mass concentrations in the final test materials was obtained by combining contributions from the homogeneity, the stability and the model SPM characterization.
The whole water materials were sufficiently homogeneous and stable at 4 °C for their intended use. In total, 12 out of 15 investigated target parameters could be assessed to be present with a relative combined expanded uncertainty below 25 %. The outcome of the two interlaboratory comparisons confirmed the good quality of the test materials and the level of uncertainties associated with the estimated mass concentrations. These findings are an important contribution towards the development of whole water matrix reference materials certified for PAH, PBDE and TBT in support of the Water Framework Directive of the European Union.
Phosphorus-fertilizers from secondary resources such as sewage sludge ash (SSA) will become more important in the future as they could substitute conventional fertilizers based on the nonrenewable resource phosphate rock. Thermochemical approaches were developed which remove heavy metals from SSA prior to its fertilizer application on farmlands. We analyzed the chemical state of mercury and selenium in SSA before and after thermochemical treatment under different conditions for P-fertilizer production by X-ray absorption near edge structure (XANES) spectroscopy. In some incineration plants the mercury loaded carbon adsorber from off-gas cleaning was collected together with the SSA for waste disposal. SSAs from those plants contained mercury mainly bound to carbon/organic material. The other SSAs contained inorganic mercury compounds which are most probably stabilized in the SSA matrix and were thus not evaporated during incineration. During thermochemical treatment, carbon-bound mercury was removed quantitatively. In contrast, a certain immobile fraction of inorganic mercury compounds remained in thermochemically treated SSA, which were not clearly identified. HgSe might be one of the inorganic compounds, which is supported by results of Se K-edge XANES spectroscopy. Furthermore, the chemical state of selenium in the SSAs was very sensitive to the conditions of the thermochemical treatment.
In 2011, the German Association of Engineers (VDI) started working on a set of guidelines towards increased resource efficiency. These guidelines represent a framework that defines resource efficiency and outlines considerations for the producing industry. A special guideline for SMEs is included as well as guidelines on methodologies for evaluating resource use indicators, such as the cumulative raw material demand of products and production systems. Resource efficiency, defined here as the ratio of specific quantifiable use to natural resource consumption, can be evaluated by defining a function which expresses the specific use and quantifies the resource requirements through a set of indicators (use of raw materials, energy, water, land and ecosystem services including sinks). The results from this also depend on the system boundary parameters and the allocation rules for by-products and waste treatment options. Optimising resource use is possible at all stages of a product’s or production system’s life cycle chain (raw material extraction, production and manufacturing, use and consumption, and the end-of-life stage). VDI guidelines are widely accepted across Germany’s industrial sector and therefore represent an important means of mainstreaming resource efficiency in this target area. As well as providing a methodological framework, the guidelines describe strategies and measures towards increasing resource efficiency, and they enable industrial producers and service providers to identify potential areas of improvement. The full article presents an overview of the methodology and contents of these guidelines and discusses their impact in achieving absolute reductions in the industrial use of natural resources.
In the last several decades, the rural exodus has led to an increasing number of inhabitants in the urban areas. The increased building and infrastructural construction caused the transformation of the landscape and to an increased land sealing in these areas. Consequently, the increased land sealing influences the air temperatures in the cities, since houses, streets and squares heat up continuously. As a result, the city and metropolitan areas became significantly warmer than their surroundings - the effect is known as Urban Heat Island (UHI). These changes have a negative impact for the quality of life. To deal with the negative effects of UHI, a high level of technical and financial effort is necessary. The costs caused by the UHI effects are in the range of several billion US dollars worldwide per year. The recent studies on UHI showed that the established methods like parks and green spaces or bright coatings for roof areas will soon not be able to effectively cope with the UHI effect in urban areas. Therefore there is a need for additional methods to mitigate UHI effect in the cities. The streets, sidewalks and squares represent approximately 30% to 40% of the inner cities areas. If these areas are designed functionally, they can have a significant impact on the UHI. This contribution focuses on development of a concrete paving stone with self-cooling properties. For the cooling effect the evaporative cooling is used. The paving stone is able to store large quantities of water and deliver during appropriate environmental conditions. This paper deals with the results of the long-term experiments on the test-fields under different climatic conditions. To interpret the test-field-results, laboratory tests were carried out as well. The paper presents and discuss the obtained results, and points out the difficulties occurred.
- Spurenelementanalytik aus Fluoreszenzlampen optimiert
- Königswasseraufschluss Methode der Wahl für REE
- Perchlorsäure-/Flusssäureaufschluss in Kombination mit Königswasseraufschluss für die meisten Elemente geeignet
- Teilweise starke Abhängigkeit der Aufschlusseffizienz vom Element bzw. der vorliegenden Elementspezies
- Nicht aufgelöste Glasmatrix stört die Analytik nicht
A biological impact on weathering was recognized already at the beginning of the twentieth century, when biochemical influence of the lichen growth on rocks was convincingly demonstrated. Later it was shown that the
progress of solid rock weathering initiated by biological colonization was affected by the initial porosity system and sensitivity of mineral association. In the meantime
a considerable amount of diverse scientific data confirm the importance of biological rock colonizers (lichens and free-living rock biofilms) in mineral material dynamics as they occur at the atmosphere-exposed rock surfaces on local as well as global scale. Subaerial rock biofilms—microbial ecosystem including free-living heterotrophic and phototrophic settlers of bare rock surfaces—are characteristic for the first stage of primary succession of terrestrial ecosystems on mineral substrates.
These cultivable and free-living communities are dominated by fungi and set the stage for the later development of a lichen cover, but in comparison to lichens also represent a new tool for laboratory experimentation and thus open a new stage of work in geomicrobiology. The Minerals sensitivity to microbially induced biological weathering can be demonstrated by studies of natural samples as well as by the laboratory mesocosm experiments.
In 2011, the German Association of Engineers (VDI) started working on a set of guidelines dealing with the improvement of resource efficiency. These guidelines represent a framework that defines resource efficiency and outlines proposals for the producing industry. A special guideline for small and medium-sized enterprises (SMEs) is included as well as guidelines on methodologies for evaluating resource use indicators, such as the cumulative raw material demand of products and production systems. The work on resource use indicators is still in progress. The evaluation of raw materials expenditure will include water, soil and land use. The model will include the availability of raw materials (criticality). Improving resource efficiency at the end-of-life stage is illustrated in this paper by the example of materials recovery from waste, here from residues out of municipal solid waste incineration (MSWI). With mechanical treatment valuable materials like ferrous and non-ferrous metals and secondary construction material can be extracted from MSWI bottom ash. The potential contribution on the resource efficiency is discussed.
Bottom ash from municipal solid waste incineration (MSWI) consists of elemental metals in considerable amounts. The exergy of bottom ash was calculated to be some 100 kJ/mol, mainly as a result of the presence of elemental Fe and Al. From this it can be shown that the recovery of elemental metals Cu, Al and Fe is beneficial. The fine fraction <4 mm additionally contains chemically bound metals (oxides, carbonates, silicates). Separation prospects with techniques as in ore processing (flotation, density separation, bioleaching, hydrothermal solution) are discussed. Although the concentration of Cu compounds in bottom ash is in the range of today’s exploited ores the economic viability of the recovery of metal compounds is uncertain. For sufficient enrichment different concerted treatment steps are required.
Mit der Parole „all liners leak“ fordern namhafte Protagonisten der US-amerikanischen Geo-kunststoffszene, dass man auch bei der Verwendung von Kunststoffdichtungsbahnen (KDB) die Deponieabdichtungen als Doppeldichtung mit Kontrolldränage ausführen muss. Dem wird von deutschen Fachleuten der „zero leakage approach“ entgegengesetzt. Danach kann unter bestimmten Voraussetzungen eine Kombinationsdichtung aus mineralischer Dichtung und KDB so gebaut werden, dass dieser „liner“ tatsächlich dicht ist und die KDB als eine echte „Konvektionssperre“ wirkt. Im deutschen Deponiebau ist man mit dieser Herangehensweise vertraut. Dennoch sollen hier nochmals die wesentlichen Elemente des „zero leakage approach“ herausgestellt werden. Auf eines dieser Elemente, die Zulassung von KDB, wird näher eingegangen. Anhand von Messungen mit Dichtungskontroll¬systemen wird dann gezeigt, dass dieser „approach“ auch funktioniert.
Gas sensors in linear form based on the measuring principle of gas selective permeability through a membrane were developed and introduced for the detection and quantification of gas concentrations. A current field study focuses on measuring CO2 concentrations for a spatially distributed monitoring of subsurface CO2 gas storage sites in near real time. A 400 m² test site and a corresponding laboratory system were built up to characterize, validate, and optimize the sensor. A calibration routine was developed, which can be applied subsequently to underground installation. First measurement results indicate the potential of the method.
Monitoring the ingestion of microplastics is challenging and suitable detection techniques are insufficiently used. Thus, misidentifying natural for synthetic microfibres cannot be avoided. As part of a framework to monitor the ingestion of microplastics in eelpout, this short report addresses the accurate identification of microfibres. We show that, following visual inspections, putatively synthetic microfibres are indeed of natural origin, as ascertained by spectrometric analyses. Consequently, we call for an inclusion of spectroscopic techniques in standardized microplastic monitoring schemes.
The reliable characterization of subsurface contamination of spatially extended contaminated sites is a challenging task, especially with an unknown history of land use. Conventional technologies often fail due to temporal and financial constraints and thus hinder the redevelopment of abandoned areas in particular. Here we compare two site screening techniques that can be applied quickly at relatively low cost, namely Direct Push (DP)-based groundwater sampling and tree core sampling. The effectiveness of both methods is compared for a rural megasite contaminated with chlorinated hydrocarbons. Unexpected pollution hot spots could be identified using both of these methods, while tree coring even enabled the delineation of the contaminant plume flowing into an adjacent wetland inaccessible for DP units. Both methods showed a good agreement in revealing the spatial pattern of the contamination. The correlation between groundwater concentrations and equivalent concentrations in wood was linear and highly significant for trichloroethene. Correlation was less obvious for its metabolite cis-dichloroethene, but still significant. As outcome of our study we recommend tree coring and for initial screening in combination with a DP sampling to retrieve quantitative data on groundwater pollutants in order to assess the contamination situation of a non- or only partly investigated site. The subsequent placement of monitoring wells for long-term monitoring of contamination levels is recommended. A combination of methods would achieve more relevant information at comparable or possibly even lower efforts in comparison to a conventional site investigation.
This report supports the implementation of European regulations on biocidal products for the product types 7, 9 and 10. Emission of active substances from material preservatives into environmental compartments can occur due precipitation. Risk characterisations have to be based on estimations of environmental concentrations of target substances leached from material preservatives. Harmonised test procedures are required to predict environmental impact due to leaching. Seventeen treated articles, mainly paints, but also a textile, sealing tapes and sealing masses were investigated by intermittent contact to water to prove suitability of the proposed laboratory test procedure. Parameters that affect leaching of active substances were examined.
Further development of a semi-analytical model to describe laboratory leaching data revealed that the model can be improved if changes of the leachability of substances during the test are supposed and integrated. Six paints and a textile were exposed to weathering to compare results from laboratory and field experiments. Similarities between leaching processes in both test approaches were observed. Generally, emissions of active substances are considerably higher in laboratory tests than from vertically installed test specimens exposed to weathering. Competing processes that cause losses of active substances can occur in both tests, but to a higher degree in field experiments. In addition, the influence of meteorological parameters on leaching processes was investigated. Factors besides the amount of driving rain were identified that effect leaching processes by complex interaction. Relations between laboratory and field data were analysed, and the applicability of the semi-analytical model was tested for field data. Guidance documents for leaching tests under laboratory and field conditions were drafted and discussed with experts on EU Level workshop 3./4. July 2014, BAM, Berlin), and are included in this Report.
Improving resource efficiency at the end-of-life stage is illustrated in this paper by the example of materials recovery from waste, here from residues out of municipal solid waste incineration (MSWI). With mechanical treatment valuable materials like ferrous and non-ferrous metals and secondary construction material can be extracted from MSWI bottom ash. The potential contribution on the resource efficiency will be discussed.
Over the past few decades, there has been an increased frequency and duration of cyanobacterial Harmful Algal Blooms (HABs) in freshwater systems globally. These can produce secondary metabolites called cyanotoxins, many of which are hepatotoxins, raising concerns about repeated exposure through ingestion of contaminated drinking water or food or through recreational activities such as bathing/swimming. An ultra-performance liquid chromatography tandem mass spectrometry (UPLC–MS/MS) multi-toxin method has been developed and validated for freshwater cyanotoxins; microcystins-LR, -YR, -RR, -LA, -LY and -LF, nodularin, cylindrospermopsin, anatoxin-a and the marine diatom toxin domoic acid. Separation was achieved in around 9 min and dual SPE was incorporated providing detection Limits of between 0.3 and 5.6 ng/L of original sample. Intra- and inter-day precision analysis showed relative standard deviations (RSD) of 1.2–9.6% and 1.3 –12.0% respectively. The method was applied to the analysis of aquatic samples (n = 206) from six European countries. The main class detected were the hepatotoxins; microcystin-YR (n = 22), cylindrospermopsin (n = 25), microcystin-RR (n = 17), micro-cystin-LR (n = 12), microcystin-LY (n = 1), microcystin-LF (n = 1) and nodularin (n = 5). For microcystins, the levels detected ranged from 0.001 to 1.51 mg/L, with two samples showing combined levels above the guideline set by the WHO of 1 mg/L for microcystin-LR. Several samples presented with multiple Toxins indicating the potential for synergistic effects and possibly enhanced toxicity. This is the first published pan European survey of freshwater bodies for multiple biotoxins, including two identified for the first
time; cylindrospermopsin in Ireland and nodularin in Germany, presenting further incentives for improved monitoring and development of strategies to mitigate human exposure.
Background: Biocidal products can be sources of active substances in surface waters caused by weathering of treated articles. Marketing and use of biocidal products can be limited according to the European Biocidal Products Regulation if unacceptable risks to the environment are expected. Leaching of active substances from treated articles was observed in field experiments to obtain information on leaching processes and investigate the suitability of a proposed test method.
Results: Leaching under weathering conditions proceeds discontinuously and tends to decrease with duration of exposure. It mainly depends on the availability of water, but is also controlled by transport processes within the materials and stability of the observed substances. Runoff amount proved to be a suitable basis to compare results from different experiments. Concentrations of substances are higher in runoff collected from vertical surfaces compared to horizontal ones, whereas the leached amounts per surface area are higher from horizontal surfaces. Gaps in mass balances indicate that additional processes such as degradation and evaporation may be relevant to the fate of active substances in treated articles. Leached amounts of substances were considerably higher when the materials were exposed to intermittent water contact under laboratory conditions as compared to weathering of vertically exposed surfaces.
Conclusions: Experiences from the field experiments were used to define parameters of a procedure that is now provided to fulfil requirements of the Biocidal Products Regulation. The experiments confirmed that the amount of water which is in contact with exposed surfaces is the crucial parameter determining leaching of substances.
In order to estimating the amount and kind of emissions from polymeric sporting tracks a laboratory test was developed in BAM that combines artificial weathering and subsequent batch and column tests [1, 2, 3]. The goal consisted in nvestigating a possible change of emissions into soil and groundwater of a new sporting ground as a function of ageing and egradation of the system. At various stages of the weathering, the samples were removed and subjected to especially designed column extraction tests for the solid samples. Both these extracts and the accumulated rainwater run-off of the weathering device were subjected to analytical tests of their ingredients. The overall aim of the test consisted in developing ontrollable, reproducible, and standardisable conditions and methods of investigation that would allow an estimation of the emissions in the course of outdoor application of about five years.
Arsenolipids (AsL) of the type arsenic-containing fatty acids (AsFA) and hydrocarbons (AsHC) are natural organoarsenic compounds present in high abundance in seafood. Since little is known about their toxicity, there is a significant concern about their health risk. Here we report the synthesis of two new AsL and their identification in fish by liquid chromatography (LC) coupled simultaneously to inductively coupled plasma mass spectrometry (ICP-MS) and to high resolution mass spectrometry (HR-MS). The molecular structure was elucidated on the basis of their exact mass and their product ion mass spectra. One of the synthesized AsL has been already identified in fish samples, meanwhile, the other arsenolipid is reported here as a natural product in fish.
Arsenic and mercury are frequent contaminants in the environment and care must be taken to limit their entrance into the food chain. The toxicity of both elements strongly depends upon their speciation. Total amounts of As and Hg as well as their species were analyzed in muscle and liver of 26 fishes of seven freshwater fish species caught in the River Elbe. The median concentrations of As were 162 mg kg-1 w.w. in liver and 92 mg kg-1 w.w. in muscle. The median concentrations of total Hg were 241 mg kg-1 w.w. in liver and 256 mg kg-1 w.w. in muscle. While this level of Hg contamination of the freshwater fish in the River Elbe is significantly lower than 20 years ago, it exceeds the recommended environmental Quality standard of 20 mg Hg kg-1 w.w. by a factor of 5e50. However, the European maximum level of 500 mg Hg kg-1 for fish for human consumption is rarely exceeded. Arsenic-containing fatty acids and hydrocarbons were determined and partially identified in methanolic extracts of the fish by HPLC coupled in parallel to ICP-MS (element specific detection) and ESI-Q-TOF-MS (molecular structure detection). While arsenobetaine was the dominant As species in the fish, six arsenolipids were detected and identified in the extracts of liver tissue in common bream (Abramis brama), die (Leuciscus idus), asp (Aspius aspius) and northern pike (Esox lucius). Four arsenic-containing fatty acids (AsFA) and two arsenic-containing hydrocarbons (AsHC) are reported in freshwater fish for the first time. With respect to mercury the more toxic MeHgþ was the Major species in muscle tissue (>90% of total Hg) while in liver Hg2þ and MeHgþ were of equal importance. The results Show the high relevance of element speciation in addition to the determination of total element concentrations to correctly assess the burden of these two elements in fish.
Two iron-based molten salts comprising an imidazolium and Schiff base were evaluated as catalysts for removal of carbamazepine (CBZ) from water. The catalysts were fully characterized using scanning electron microscopy (SEM), energy-dispersive X-ray spectrometry (EDX), nuclear magnetic resonance spectroscopy (NMR), electrospray ionisation–mass spectrometry (ESI–MS), differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR) and nitrogen adsorption–desorption isotherms (BET). Additionally, the formation of photo-sensitized oxygen was investigated by spin-trapping using electron spin resonance (ESR). The catalytic activity in heterogeneous oxidation of the micropollutant (CBZ) was also evaluated. The effects of catalyst loading, pH, H2O2 dosage and UV light on the oxidation of the selected compound were investigated. After 15 min of UVA irradiation in the presence of 200 μM H2O2, CBZ was completely removed over both catalysts.
Die VDI-Richtlinie 3925 entstand aus Diskussionen und Fragestellungen, die sich aus der Anwendung unterschiedlichster Methoden zur Bewertung verschiedener
Verfahrenskonzepten aus dem Bereich der Abfallbehandlung ergeben haben. Je nach nachdem, wo der Focus der vorzunehmenden Bewertung liegt, wird sich die Methodik an diese Ziele anpassen oder - falls es die entsprechende Methodik noch nicht geben sollte - sich die Fragestellung anpassen müssen.
Towards the standardization of biochar analysis: the COST action TD1107 interlaboratory comparison
(2016)
Biochar produced by pyrolysis of organic residues is increasingly used for soil amendment and many other applications. However, analytical methods for its physical and chemical characterization are yet far from being specifically adapted, optimized, and standardized. Therefore, COST Action TD1107 conducted an interlaboratory comparison in which 22 laboratories from 12 countries analyzed three different types of biochar for 38 physical–chemical parameters (macro- and microelements, heavy metals, polycyclic aromatic hydrocarbons, pH, electrical conductivity, and specific surface area) with their preferential methods. The data were evaluated in detail using professional interlaboratory testing software. Whereas intralaboratory repeatability was generally good or at least acceptable, interlaboratory reproducibility was mostly not (20% < mean reproducibility standard deviation < 460%). This paper contributes to better comparability of biochar data published already and provides recommendations to improve and harmonize specific methods for biochar analysis in the future.
The need for technological progress in bio-diagnostic assays of high complexity requires both fundamental research and constructing efforts on nano-scaled assay recognition elements that can provide unique selectivity and design-enhanced sensitivity features. Nanoparticle induced sensitivity enhancement and its application related to multiplexed capability Surface-Enhanced InfraRed Absorption (SEIRA) assay formats are well suitable for these purposes. The potential of diverse fluorophore–antibody conjugates, being chemisorbed onto low-cost gold nanoparticulate SEIRA substrates, has been explored with respect to their spectral discriminability. These novel biolabels deliver molecular SEIRA fingerprints that have been successfully analyzed by both uni- and multivariate analyzing tools, to discriminate their multiplexing capabilities. We show that this robust spectral encoding via SEIRA fingerprints opens up new opportunities for a fast, reliable and multiplexed high-end screening in biodiagnostics.
Fluorescence lamps contain considerable amounts of rare earth elements (REE). Several recycling procedures for REE recovery from spent lamps have been established. However, despite their economic importance, the respective recycling is scarce so far, with an REE recovery rate of less than 1%. A reliable analysis of REE and other relevant metals like Yttrium is crucial for a thorough and complete recovery process. This applies both to the solid matter and aqueous phase, since most of the recycling processes include wet-chemical steps. We tested seven different reagent mixtures for microwave-assisted digestion of fluorescent lamp shredder, including hydrofluoric acid, perchloric acid, and hydrogen peroxide. We determined the concentrations of 25 of the most relevant rare earth and other trace elements (Al, P, Ti, V, Cr, Fe, Ni, Cu, Ga, Ge, As, Y, Ag, Cd, Sn, Sb, La, Ce, Eu, Gd, Tb, W, Au, Hg, and Pb) in the respective dilutions. Two independent digestions, one a mixture of perchlorid/nitric/hydrofluoric acid and the other aqua regia, showed the highest concentrations of 23 of these elements, excluding only Sn and Tb. The REE concentrations in the tested lamp shredder sample (stated in g/kg) were 10.2 (Y), 12.1 (La), 7.77 (Ce), 6.91 (Eu), 1.90 (Gd), and 4.11 (Tb).
Anticancer drugs (ACDs) exhibit high biological activity, they are cytotoxic, genotoxic, and are constantly released into the environment as a result of incomplete metabolism. Consequently they pose a serious threat to the environment and human health due to their carcinogenic,mutagenic and/or reproductive toxicity properties. Knowledge of their bioavailability, including their sorption to soils and their impact on the soil–groundwater pathway, is crucial for their risk assessment. Laboratory batch and column leaching tests are important tools for determining the release potential of contaminants from soil or waste material. Batch and column tests were carried out with soils differing in physicochemical properties, each spiked with cyclophosphamide (CK) or ifosfamide (IF). Moreover, due to the fact that environmental pollutants may occur as coexisting compounds in the soil themobility evaluation for ACDs in the mixture with metoprolol (MET; β-blocker) as a co-contaminant was performed. In order to assess appropriateness, the batch and column tests were compared. The release depended on the properties of both the soil and the presence of co-contaminants. The faster release was observed for coarse-grained soil with the smallest organic matter content (MS soil: 90% decrease in concentration until liquid-to-solid ratio (L/S) of 0.3 L kg−1 for all tests' layout) than for loamy sand (LS soil: 90% decrease in concentration until ratio L/S of 0.75 L kg−1). ACDs are highly mobile in soil systems. Furthermore, the decrease of mobility of ifosfamide was observed with the presence of a co-contaminant (metoprolol) in both of the soils (in MS soil a decrease of 29%; in LS soil a decrease of 26%). The mobility of cyclophosphamide does not depend on the presence of a contaminant for MS soil, but also exhibits a decrease of 21% in LS soil.
Within a class of agrochemical residues, pesticides are significant concern due to their various adverse effects on people, animals and the environmental systems. Once they entered to food or to the environment, the parent compound is transformed to metabolites which have different toxicity profiles. Activities like food cooking and waste water treatment (WWT) may lead to produce more toxic metabolites than the parent substances.
Online coupling of electrochemistry with liquid chromatography mass spectrometry (EC-HPLC-MS) is one of the most promising and powerful techniques for metabolite studies which exploited widely for pharmaceuticals so far [1]. However, data on the application of EC-HPLC-MS to simulate environmental transformation products, the fate of contaminants and their metabolic pathways are rare. The oxidation of analyte of interest on the EC, separate the metabolites on HPLC and identifying them by MS gives enormous advantages to identify the contaminants transformation products [2]. Thus, applying this technique (EC-MS, EC-HPLC-MS, and HPLC-EC-MS) for transformation products of pesticide residues is urgently needed.
The main interest of this study will be investigating the electrochemical oxidative degradation products, simulating to in-vitro metabolites and transformation processes of selected pesticides in food and environmental samples. The parent pesticides’, like carbamates and abamectin, oxidation by EC, product metabolites identification and their fates will be discussed using electrochemistry coupled to HPLC-MS techniques.
Task allocation in social insect colonies is generally organised into an age-related division of labour, termed the temporal polyethism schedule, which may in part have evolved to reduce infection of the colony's brood by pests and pathogens. The temporal polyethism schedule is sensitive to colony perturbations that may lead to adaptive changes in task allocation, maintaining colony homeostasis. Though social insects can be infected by a range of parasites, little is known of how these parasites impact within-colony behaviour and the temporal polyethism schedule. We use honey bees (Apis mellifera) experimentally infected by two of their emerging pathogens, Deformed wing virus (DWV), which is relatively understudied concerning its behavioural impact on its host, and the exotic microsporidian Nosema ceranae. We examined parasite effects on host temporal polyethism and patterns of activity within the colony. We found that pathogens accelerated the temporal polyethism schedule, but without reducing host behavioural repertoire. Infected hosts exhibited increased hyperactivity, allocating more time to self-grooming and foraging-related tasks. The strength of behavioural alterations we observed was found to be pathogen specific; behavioural modifications were more pronounced in virus-treated hosts versus N. ceranae-treated hosts, with potential benefits for the colony in terms of reducing within-colony transmission. Investigating the effects of multiple pathogens on behavioural patterns of social insects could play a crucial role in understanding pathogen spread within a colony and their effects on colony social organisation.
Phosphorus (P) for fertilizer use can be recovered from sewage sludge ash (SSA). To enhance the bioavailability of P and reduce the heavy metal content of SSA, it can be treated thermochemically with Na2CO3 or Na2SO4 at 950 °C in a rotary kiln using dry sewage sludge or lignite as reducing agent. These processes were investigated by thermogravimetry/differential thermal analysis coupled with gas analysis. Reducing conditions in this experimental setup were provided by 2 % hydrogen in the Ar carrier gas. During SSA + Na2CO3 treatment CO2, CO and water were detected in the off-gas. During SSA + Na2SO4 treatment SO2, some CO2 and water were detected. Heavy metal removal was more efficient for SSA + Na2CO3 compared to the sulfate variant. A SSA + Na2SO4 + lignite variant which also formed CO shifted the heavy metal removal to the results obtained with Na2CO3 which was obviously due to the additional reduction potential. However, Zn evaporation was not achieved with the Na2SO4 variants which were most probably due to immobilization as ZnS.
Sewage sludge incineration is extensively practiced in some European countries such as the Netherlands, Switzerland, Austria and Germany. A survey of German sewage sludge ash showed that the recovery potential is high, approx. 19,000 t of phosphorus per year. However, the survey also discovered that the bioavailability of phosphorus in the sewage sludge ash is poor and that more than half of the ashes cannot be used as fertilizers due to high heavy metal content. A new thermochemical process for sewage sludge ash treatment was developed that transforms the ash into marketable fertilizer products. Sewage sludge ash was thermochemically treated with sodium and potassium additives under reducing conditions, whereby the phosphate-bearing mineral phases were transformed into plant available phosphates. High P-bioavailability was achieved with a molar Na/P ratio > 1.75 in the starting materials. Sodium sulfate, carbonate and hydroxide performed comparably as additives for this calcination process. Potassium carbonate and -hydroxide have to be added in a molar K/P ratio > 2.5 to achieve comparable P-solubility. The findings of the laboratory scale investigations were confirmed by an industrial demonstration trial for an ash treatment with sodium sulfate. Simultaneously, the volatile transition metal arsenic (61% removal) as well as volatile heavy metals such as cadmium (80%), mercury (68%), lead (39%) and zinc (9%) were removed via the off-gas treatment system. The product of the demonstration trial is characterized by high bioavailability and a toxic trace element mass fraction below the limit values of the German fertilizer ordinance, thus fulfilling the quality parameters for a P-fertilizer.
In Germany, a quantity of more than 10 million metric tons of masonry rubble is generated per year. With regard to a sustainable closed substance cycle waste management, these rest masses have to be recovered if possible. The end-of-life (EOL) phase of masonry includes the planning steps of demolition, processing and application. The choice of the most sustainable solution raises questions regarding material technology, plant engineering, economic efficiency and ecological issues. For this purpose, a methodological concept for a holistic assessment of the EOL phase of masonry is developed within the scope of a doctoral thesis. For the assessment the Cost-Effectiveness Analysis (CEA) is adapted. The assessment concept enables a holistic comparison of different EOL scenarios for masonry while integrating all planning steps. It combines Material Flow Analysis (MFA), Life Cycle Analysis (LCA), Life Cycle Working Environment (LCWE), economic evaluation methods and material testing. In future, various scenarios can be evaluated with regard to the goals of the European and German waste management industry.
Alkaline reactions of paper sludge combustion ash at low temperature (60 °C) were performed using a calcite-rich paper ash (PA 1) and a gehlenite-rich ash (PA 2). Strong alkaline conditions (8, 12, 16 M NaOH) were revealed at reaction times of 1–4 h and 12–24 h. Reactions were performed with pure ashes and in the presence of NaAlO2. The products were characterized by XRD, FTIR, SEM/EDX, gravimetry and chemical analysis. The conversion was found to proceed mainly in the period between 1 and 4 h. Portlandite and hydrogarnet were observed from PA 1 in 8 M NaOH. Onset of formation of Ca4Al2O6CO·311H2O beside Ca(OH)2 could be analyzed after reaction of PA 1 in 12 M and 16 M NaOH. Addition of NaAlO2 favored crystallization of hydrogarnet and Ca4-Al2O6CO·311H2O. For PA 2 gehlenite remained stable, but a high portlandite fraction was observed. Addition of NaAlO2 yielded hydrogarnet beside gehlenite in 8 M NaOH. Higher alkalinities favored crystallization of Ca4Al2O6-CO·311H2O and onset of dissolution of gehlenite. Finally transformation of Ca4Al2O6CO·311H2O into sodium aluminum silicate hydrate was observed. All results were discussed with regard to heavy metal distribution of the initial PA between the alkaline digestion solution and the products. In conclusion suitable applications of the products were proposed.
Die Studie gibt einen Überblick über den Umfang und die Struktur der Gefahrgutbeförderung auf Binnenschiffen und stellt die maßgeblichen sicherheitstechnischen Vorschriften dar. Aus dem Unfallgeschehen läßt sich entnehmen, daß in West-Deutschland jährlich ca. 1200 Binnenschiffsunfälle mit größenordnungsmäßig insgesamt 100 bis 300 m³ Ladungsaustritt verbunden sind, wozu fast ausschließlich Mineralölprodukte gehören, und zumeist ein oder zwei Unfälle den größten Beitrag liefern. Während nach Unfällen häufig mit Erfolg Ölsperren zur Begrenzung von Gewässerverunreinigungen eingesetzt werden können, führen ungeklärte Entsorgungsprobleme zu wesentlich kritischer einzuschätzenden, verdeckten Verunreinigungen der Gewässer. Insbesondere die Entsorgung von Ladungsresten bedarf in technischer, administrativer und wirtschaftlicher Hinsicht einer zufriedenstellenden Klärung wie sie z. B. bei der Bilgenwasserentsorgung existiert.
Determining a pore structure’s mechanical and chemical data on lime rendering exposed
outdoors and including masonry in the laboratory, with regard to their behaviour on moisture
transport and weathering was the objective. In search of clues for a dose-response relation -
i.e. upon a connection between the emission rate of SO2 and NOx on one hand and the degree
of damage to mainly plaster having a lime component on the other - it has been of interest to
what extent their structural characteristics including pore space are modified and so
consequently also physico-technical properties and chemical composition. For determining
corresponding criteria, a widely diversified spectrum of test methods such as to obtain data
concerning porosity and moisture transport, mechanical behaviour, and chemistry as well is
available. A description of the manufacture of plate-shaped rendering specimens with lime
putty, industrially hydrated lime and dolomitic hydrate (the last two also having a cement
admixture) and also hydraulic lime as binding agents is included. First deposition velocity and
absorption rate for SO2 were determined in laboratory tests on these materials in dry and
moist states. After their exposure on outdoor racks at six locations in the Berlin region with
differing SO2 atmospheric contents over at least 5 years, the samples of course show timedependent
modifications of chemical and physical qualities which are especially reflected in
the form of profiles of structure, strength and concentration, e.g. for sulphate. Local climatic
differences, however, partly exert a greater influence on material than emissions. Similar
investigations were performed on samples of comparable composition exposed 4 and 17
years. But the real surprise is furnished by the renderings’ behaviour depending upon
orientation and upon height at a building. Since weathering behaviour and moisture transport
(absorption, storage, release) are directly interdependent, further criteria are necessary for a
critical assessment of a plasters’ pore structure. Starting from sands, plasters were
characterized. The structural parameters were lastly influenced by the respective contents of
sand, binder and mixing water. These results and those gained from bricks naturally find their
expression in masonry sections manufactured there from, and above all in their capillary and
evaporative behaviours, and also when applying different test liquids. Summary and cited
literature is given at the end of this report.
Die im In- und Ausland vorliegenden Forschungsarbeiten zur Kostenabschätzung der immissionsbedingten Materialschäden beruhen auf zwei ökonomischen Bewertungsverfahren. Bewertungsgrundlage des einen Verfahrens sind die in Labor- und Freibewitterungsversuchen ermittelten physikalisch-chemischen Dosis-Wirkungs-Beziehungen zwischen dem Schadstoffgehalt der Luft und den schadensanfälligen Materialien. Die andere Methode geht von den Unterschieden im Instandsetzungverhalten in Abhängigkeit vom Standort (Industrie-, Stadt- und Landatmosphäre) der Sachgüter aus.
Die ökonomische Bewertung der immissionsbedingten Materialschäden der Sachgütergruppen Freileitungsmaste, Brücken der Bundesautobahnen, Eisenbahnbrücken und -fahrleitungsmaste, fernmeldetechnische Einrichtungen der Deutschen Bundespost, Industrieanlagen, Wohngebäude und Denkmäler basiert auf sogenannten „Stock-at-risk“-Informationen, Dosis-Wirkungs-Funktionen der der Atmosphäre ausgesetzten Werkstoffe und auf in der Praxis vorliegenden Erfahrungswerten über Zeitintervalle der Erneuerung der Korrosionsschutzsysteme und Bauteile. In jenen Fällen, in denen der immissionsbedingte Anteil am Gesamtschaden noch nicht eindeutig nachgewiesen werden konnte, werden die Forschungslücken aufgezeigt bzw. Modellrechnungen durchgeführt.
Mit der überarbeiteten Version der Vergabegrundlagen des Umweltzeichens Blauer Engel für Bürogeräte mit Druckfunktion (RAL-UZ 171:2012) wurde für die Partikelemission ein Prüfverfahren und ein Prüfwert eingeführt. Dies ergänzt die zahlreichen anderen Kriterien, die bereits Voraussetzungen für die Vergabe des Blauen Engels an Bürogeräte mit Druckfunktion waren. Die Anwendung des Prüfwertes für Partikelemissionen wurde von der Jury Umweltzeichen in 2012 zunächst nur für Geräte unterhalb 250 l Volumen - sogenannte Tischgeräte - beschlossen. Für größere Geräte (> 250 l, sogenannte Standgeräte) wurde eine Dokumentation des Messergebnisses im Rahmen des Prüfberichtes festgelegt. Ein Grund für diese Unterscheidung war die Tatsache, dass zu diesem Zeitpunkt für die Standgeräte keine für eine sinnvolle Festlegung eines Prüfwerts ausreichende Zahl an Messwerten und keine Erfahrungen aus entsprechenden Emissionsprüfungen vorlagen. Notwendig zur beabsichtigten Festlegung des Prüfwerts für die Partikelemission aus großen Bürogeräten war deshalb die systematische Erfassung und Bewertung der durch die anerkannten Prüfinstitute nach Inkrafttreten der RAL-UZ 171 ermittelten Ergebnisse. Dies wurde in diesem Forschungsprojekt durchgeführt. Das Forschungsprojekt befasste sich des Weiteren mit der Ermittlung und Beurteilung der Qualität der Partikelemissionsprüfungen auf Basis der zur Verfügung stehenden Prüfberichte in beiden Größenkategorien. Im Ergebnis stellte sich heraus, dass die Qualität der Prüfungen der Partikelemission insgesamt mit einer Fehlerquote von 3 % ungültiger Prüfungen sehr gut war. Ein weiteres Ergebnis ist, dass keine prüfmethodischen oder qualitätsrelevanten Gründe gegen die Anwendung des bestehenden Prüfwerts auf große Bürogeräte sprechen.
Vor dem Hintergrund der anhaltenden öffentlichen Diskussion um mögliche gesundheitliche Risiken von Ultrafein- und Feinstaubemissionen aus Bürogeräten mit Laserdruckfunktion (LPD, Laser Printing Device) wurde vom Umweltbundesamt ein Forschungsvorhaben zur Entwicklung einer Prüfprozedur für die Quantifizierung der emittierten Partikel durch Zählung unter Standardbedingungen in Emissionsmesskammern, sowie zur physikalischen und chemischen Charakterisierung dieser Aerosole initiiert. Als Ergebnis konnte die Partikelzählung in den Entwurf des Prüfverfahrens für die Bestimmung von Emissionen (RAL-UZ-122, Anhang S-M) des Umweltzeichens "Blauer Engel" für Bürogeräte sowie in den Prüfstandards ECMA-328 und den Entwurf der ISO/IEC 28360 integriert werden. Die Methode wurde in einem internationalen Ringversuch erfolgreich getestet. Auf dieser Basis können Vergabekriterien und -werte für die Emission von Fein- und Ultrafeinpartikeln im Rahmen der Vergabe des Umweltzeichens Blauer Engel vereinbart und Produktprüfungen vorgenommen werden.