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- 2016 (8) (entfernen)
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- Phosphorus recovery (4)
- Sewage sludge ash (4)
- Heavy metal evaporation (2)
- Rare earth elements (2)
- Reducing conditions (2)
- Thermochemical treatment (2)
- Bioavailability (1)
- Critical raw materials (1)
- Düngemittelanalytik (1)
- Elemental analysis (1)
Eingeladener Vortrag
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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.
Die europäische Kommission (Generaldirektion Unternehmen und Industrie) hat kürzlich die Auswirkungen einer harmonisierten europäischen Düngemittelverordnung, einschließlich der technischen Durchführbarkeit und den umweltbezogenen, wirtschaftlichen und sozialen Auswirkungen einer solchen Gesetzgebung untersuchen lassen. Basierend auf diesen Ergebnissen soll nun die EU-Düngemittelverordnung (EG) 2003/2003 revidiert werden. Neben der Vielzahl von bestehenden und neuen Düngemitteltypen wie z.B. Phosphor-Recyclingdüngern soll die neue Verordnung auch organische Düngemittel und somit Matrices wie Klärschlamm, Gärrückstände und Wirtschaftsdünger regeln. Dies bedeutet, dass Parameter und Grenzwerte, die bisher in verschiedenen Verordnungen für verschiedene Matrices geregelt wurden, künftig gemeinschaftlich geregelt werden (Klärschlamm, Düngemittel) und weitere Matrices zusätzlich geregelt werden müssen (Phosphor-Recycling-Produkte, Produkte aus Klärschlamm/-aschen).
Resultierend aus den aktuellen nationalen Entwicklungen insbesondere bezüglich des Ausstiegs aus der landwirtschaftlichen Klärschlammverwertung und im Hinblick auf die Bestrebungen hinsichtlich der Schonung natürlicher Ressourcen (z.B. ProgRess) ist zu erwarten, dass die Anzahl an Düngemitteln, die aus Recyclingmaterialien gewonnen werden, stark zunehmen wird. Recyclingdünger aus dem Stoffstrom Klärschlamm- bzw. Klärschlammasche werden zukünftig einen großen Anteil an diesen neuen Produkten ausmachen.
Vor den angeführten Hintergründen ist es notwendig relevante und insbesondere bereits genormte Verfahren hinsichtlich ihrer Anwendbarkeit auf z.B. Klärschlamm/-aschen und daraus gewonnenen Recycling-Düngern sowie auf kommerzielle P-Düngemittel zu prüfen.
Vor diesem Hintergrund wurde die BAM (FB 4.4) vom UBA mit einer Untersuchung beauftragt:
UFOPLAN FKZ: 3714263200
„Untersuchung der Anwendbarkeit der im Rahmen des CEN-Projekts HORIZONTAL entwickelten Analyseverfahren auf Düngemittel und Klärschlamm/ -aschen“
Laufzeit: 01.07.2014 – 31.01.2017
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).
The annual demand of phosphorus (P) for fertilizer use is more than 550,000 t in Germany. Several of the input streams like mineral fertilizer produced from phosphate rock or sewage sludge are problematic due to contamination with heavy metals and organic pollutants and/or supply risks. Phosphorus recovery from the wastewater stream might help to diminish these problems. Several procedures have been developed to recover P from either sewage sludge ash (SSA) or wastewater via precipitation or crystallization as struvite. This study determined the elemental composition and trace metal mass fractions of 252 SSA samples and 17 struvite samples from wastewater treatment plants (WWTP) to see whether there are differences related to the source of the sludge (municipal/industrial) or the stage of the WWTP where the struvite is produced. Results indicated that there is no clear trend of the elemental mass fractions related to the source of the sludge. All struvite samples show very low heavy metal contents, even though the struvite precipitated from the sludge shows slightly elevated heavy metal mass fractions compared to struvite crystallized from sludge liquor. Struvite is a clean and plant available material for fertilizer production from wastewater streams and has some advantages for the wastewater treatment plant. However, since the P recovery rate of struvite processes is low (7–11%) compared to that from SSA processes (90%), recovery from SSA is necessary for a substantial P recovery from the wastewater stream.
Recovery of rare earth elements - optimized elemental analysis of fluorescent lamp shredder waste
(2016)
Rare earth elements (REE) are a crucial component of fluorescence lamps. Several procedures have been developed to recovery these technological important elements. Nevertheless, actual REE recycling from fluorescence lamps is scarce so far (recovery rate of less than 1 %), with current recycling approaches concentrating on glass recovery. Since most recycling processes include several, also wet-chemical steps, a complete knowledge of the actual elemental composition of the respective mass flows is necessary for an efficient REE recovery. We tested seven different reagent mixtures for microwave-assisted digestion of fluorescent lamp shredder, including HF, HClO4, and H2O2. We determined the concentrations of 25 of the most relevant rare earth and other trace elements 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).
- 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
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.
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.