4 Material und Umwelt
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Organisationseinheit der BAM
- 4.3 Schadstofftransfer und Umwelttechnologien (249) (entfernen)
Paper des Monats
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Eingeladener Vortrag
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Throughout their life cycles—from production, usage, through to disposal—materials and products interact with the environment (water, soil, and air). At the same time, they are exposed to environmental influences and, through their emissions, have an impact on the environment, people, and health. Accelerated experimental testing processes can be used to predict the long-term environmental consequences of innovative products before these actually enter the environment.
We are living in a material world. Building materials, geosynthetics, wooden toys, soil, nanomaterials, composites, wastes and more are research subjects examined by the authors of this book. The interactions of materials with the environment are manifold. Therefore, it is important to assess the environmental impact of these interactions. Some answers to how this task can be achieved are given in this Special Issue.
Per- and polyfluoroalkyl substances (PFAS) are a large group of anionic, cationic, or zwitterionic organofluorine surfactants used in the formulations of thousands of products and consumer goods, including aqueous film-forming foams (AFFF) used to suppress aviation fires in training scenarios, non-stick cookware, fast-food wrappers, water-repellent fabrics, medical equipment. Because PFAS have been extensively used in a variety of AFFF products they can be found in soils from industrial and military installations. Current decontamination strategies of PFAS-burdened soils mainly consist of adsorption methods using adsorbents for fixation of PFAS in the ground. A second option is the utilization of a “pump and treat” process, cycling polluted soils through a washing plant leading to the concentration of the pollutants in the fine fraction. Only a subsequent, high-energy consuming pyrolysis process guarantees the total destruction of all fluorinated organic contaminants. Both approaches are cost-intensive and not intended for the direct decomposition of all PFAS contaminants. Hence, there is a great demand for innovative developments and chemical treatment technologies, dealing with new strategies of tackling the PFAS problem. Previously, mechanochemical treatment of polychlorinated organic compounds in soils showed an efficient dechlorination. Thus, we investigated mechanochemical treatment of PFAS contaminated soils with various additives in a ball mill and analyzed the PFAS defluorination with gas chromatography mass spectrometry (GCMS) and liquid chromatography tandem mass spectrometry (LC-MS/MS), respectively, as well es the fluoride mineralization by ion chromatography (IC) and fluorine K-edge X-ray absorption near-edge structure (XANES) spectroscopy.
Current decontamination strategies of PFAS-burdened soils mainly consist of adsorption methods using adsorbents for fixation of PFAS in the ground. A second option is the utilization of a “pump and treat” process, cycling polluted soils through a washing plant leading to the concentration of the pollutants in the fine fraction. Only a subsequent, high-energy consuming pyrolysis process guarantees the total destruction of all fluorinated organic contaminants. These approaches are cost-intensive and not intended for the direct decomposition of all PFAS contaminants. Hence, there is a great demand for innovative developments and chemical treatment technologies, dealing with new strategies of tackling the PFAS problem. Thus, we investigated mechanochemical treatment of PFAS contaminated soils with various additives in a ball mill and analyzed the PFAS defluorination with gas chromatography mass spectrometry (GC-MS) and liquid chromatography tandem mass spectrometry (LC-MS/MS), respectively, as well as the fluoride mineralization by ion chromatography (IC) and fluorine K-edge X-ray absorption near-edge structure (XANES) spectroscopy.
Municipal solid waste incineration (MSWI) is one of the leading technologies for municipal solid waste (MSW) treatment in Europe. Incineration bottom ash (IBA) is the main solid residue from MSWI, and its annual European production is about 20 million tons. The composition of IBA depends on the composition of the incinerated waste; therefore, it may contain significant amounts of ferrous and non-ferrous (NFe) metals as well as glass that can be recovered. Technologies for NFe metals recovery have emerged in IBA treatment since the 1990s and became common practice in many developed countries. Although the principles and used apparatus are nearly the same in all treatment trains, the differences in technological approaches to recovery of valuable components from IBA – with a special focus on NFe metals recovery – are summarized in this paper.
Angesichts stetig steigender Rohstoffnachfrage und sich verknappenden Ressourcen rücken Sekundärrohstoffe zur Deckung des Bedarfes immer stärker in den Fokus.
Besonders Hausmüllverbrennungsaschen (HMVA) verfügen über hohe Anteile an Metallen wie Aluminium, Kupfer, oder Eisen, aber auch Spuren von Silber und Gold.
Aus diesem Grund wurde bereits in einer Vielzahl von Arbeiten und Projekte die Behandlung von Rostaschen diskutiert. Hauptaugenmerk der Betrachtungen ist die Rückgewinnung von Wertstoffen, insbesondere der Metallfraktion, sowie die Aufbereitung der Rostasche als Ersatzbaustoff. Die bisherigen Betrachtungen konzentrierten sich auf die Fraktionen der Partikel größer 2 mm. Die Feinfraktion kleiner 2 mm wurde bislang meist deponiert. Da die Feinfraktion etwa 25 M% der
HMVA ausmacht, wurde für weitere Untersuchungen zum Zweck einer besseren Verwertung das Projekt „BASH-TREAT“ im Programm ERA-MIN 2 initiiert.
Die Umweltverträglichkeit von Bauprodukten, die in Kontakt mit Regen- oder Sickerwasser kommen, wurde durch Kombination normierter Elutions- (DSLT, Perkolationstest) und Ökotoxizitätstests (Algen, Daphnien, Fischeier, Leuchtbakterien) sowie Gentoxizitätstests (Ames, umu) untersucht. Ziel des Projektes war es einerseits, einen Beitrag zur Harmonisierung der Prüfmethoden unter CEN/TC 351 zu leisten und andererseits potentielle Produktgruppen, die sich für die Umweltzeichenvergabe des Blauen Engels eignen würden, zu erkennen. Durch umfangreiche qualitative und quantitative chemische Analysen (u. a. GC-MS- sowie LC-MS-Screening) wurden einige der freigesetzten Stoffe identifiziert und anhand von Literaturdaten ökotoxikologisch charakterisiert. Insgesamt wurden 34 Bauprodukte (Dachbahnen, Lacke, Wood-Plastic-Composites, Pflasterfugenmörtel, Korkgranulate, Schaumglasschotter, Wegedecken, Dichtmassen) untersucht. Hierbei wurden insbesondere bei den Fugenmörteln und Korkgranulaten sehr hohe
Ökotoxizitäten (bis LID = 16384 bei den Fugenmörteln und LID = 24578 bei den Korkgranulaten) beobachtet. Algen- und Leuchtbakterientests waren in der Regel deutlich empfindlicher als der Daphnien- und Fischeitest. Die untersuchten Dachbahnen, Lacke, Wood-Plastic-Composites und Schaumglasschotter zeigten hingegen keine oder nur sehr geringe Ökotoxizitäten. Zur Qualitätssicherung und Validierung wurde ein Europäischer Ringversuch gemäß den Vorgaben der DIN ISO 5725 organisiert, durchgeführt und ausgewertet. Hierzu wurde ein Fugenmörtel als flächiges Produkt im DSLT und als gebrochenes körniges Produkt im Perkolationstests eluiert und die Eluate nachfolgend in den 29 teilnehmenden Laboren hinsichtlich ihrer Ökotoxizität untersucht. Hierbei wurden insgesamt plausible Ergebnisse und gute (<50 %) bis sehr gute (<20 %) Reproduzierbarkeiten erzielt. Es wird empfohlen, für die Produktgruppen Dachbahnen, Kunstrasen und Sportböden sowie Fugenmörtel Vergabekriterien für den Blauen Engel zu entwickeln
Microspectroscopy reveals dust-derived apatite grains in acidic, highly-weathered Hawaiian soils
(2021)
Dust deposition is an important source of phosphorus (P) to many ecosystems. However, there is little evidence of dust-derived P-containing minerals in soils. Here we studied P forms along a well-described climatic Gradient on Hawaii, which is also a dust deposition gradient. Soil mineralogy and soil P forms from six sites along the climatic gradient were analyzed with bulk (X-ray diffraction and P K-edge X-ray absorption near edge structure) and microscale (X-ray fluorescence, P K-edge X-ray absorption near edge structure, and Raman) analysis methods. In the wettest soils, apatite grains ranging from 5 to 30 μm in size were co-located at the micro-scale with quartz, a known continental dust indicator suggesting recent atmospheric deposition. In addition to co-location with quartz, further evidence of dust-derived P included backward trajectory modeling indicating that dust particles could be brought to Hawaii from the major global dust-loading areas in central Asia and northern Africa. Although it is not certain whether the individual observed apatite grains were derived from long-distance transport of dust, or from local dust sources such as volcanic ash or windblown fertilizer, these observations offer direct evidence that P-containing minerals have reached surface layers of highly-weathered grassland soils through atmospheric deposition.
Dust deposition is an important source of phosphorus (P) to many ecosystems. However, there is little evidence of dust-derived P-containing minerals in soils. Here we studied P forms along a well-described climatic gradient on Hawaii, which is also a dust deposition gradient. Soil mineralogy and soil P forms from six sites along the climatic gradient were analyzed with bulk (X-ray diffraction and P K-edge X-ray absorption near edge structure)
and microscale (X-ray fluorescence, P K-edge X-ray absorption near edge structure, and Raman) analysis methods. In the wettest soils, apatite grains ranging from 5 to 30 μm in size were co-located at the micro-scale with quartz, a known continental dust indicator suggesting recent atmospheric deposition. In addition to colocation with quartz, further evidence of dust-derived P included backward trajectory modeling indicating that dust particles could be brought to Hawaii from the major global dust-loading areas in central Asia and northern Africa. Although it is not certain whether the individual observed apatite grains were derived from long-distance transport of dust, or from local dust sources such as volcanic ash or windblown fertilizer, these observations offer direct evidence that P-containing minerals have reached surface layers of highly-weathered grassland soils
through atmospheric deposition.
The concept of circular economy supports mitigation of climate change and other environmental pressures to the planet. Circulating materials in anthropogenic processes come with the risk of accumulating hazardous substances and compounds. In this concept, waste incineration or waste-to-energy (WtE) is a necessary technology to remove these compounds from the life cycle. In this mini-review, contaminants of major importance in the flue gas from waste incineration plants and their environmental impact are discussed. Air pollution of WtE is often seen as the most relevant environmental impact of this treatment option. The emission values parameter set for different countries is presented and compared. The most stringent legally set of emission values could be found in parts of Europe and South Korea. Japan also permits similar strict values when authorising individual incineration plants. In North America, the values are partially less strict as the best available technologies in Europe suggest being possible. Emerging economies, such as India and China, have shown efforts to improve their environmental protection standards but still have room to improve. This could be set in relation to other industrial emitting processes and therefore could be used to assess the relevance of this industry sector to the national emission inventories.