TY - JOUR A1 - Krüger, Oliver A1 - Adam, Christian A1 - Hobohm, J. A1 - Basu, S. A1 - Kuchta, K. A1 - van Wasen, Sebastian T1 - Recycling oriented comparison of mercury distribution in new and spent fluorescent lamps and their potential risk N2 - This study compares the mercury distribution in the vapor phase, the phosphor powder and the glass matrix of new and spent fluorescent lamps. The spent fluorescent lamps were obtained at the collection yards of a public waste management company in Hamburg, Germany. An innovative systematic sampling method is utilized to collect six spent and eight corresponding new, off-the-shelf fluorescent lamp samples. The efficiency of several acid digestion methods for the determination of the elemental composition was studied and elemental mass fractions of K, Na, Y, Ca, Ba, Eu, Al, Pb, Mg, Hg, and P were measured. The study also finds aqua regia to be the best reagent for acid digestion. However, no significant difference in mercury distribution was found in the different phases of the new and spent fluorescent lamps. KW - Mercury KW - Rare earth elements KW - Hg distribution KW - Fluorescence lamps PY - 2017 DO - https://doi.org/10.1016/j.chemosphere.2016.11.104 SN - 0045-6535 SN - 1879-1298 VL - 169 SP - 618 EP - 626 PB - Elsevier AN - OPUS4-38481 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Peplinski, Burkhard A1 - Adam, Christian A1 - Adamczyk, Burkart A1 - Müller, Ralf A1 - Michaelis, Matthias A1 - Krahl, T. A1 - Emmerling, Franziska T1 - Nanocrystalline and stacking-disordered beta-cristobalite AlPO4: the now deciphered main constituent of a municipal sewage sludge ash from a full-scale incineration facility N2 - For the first time evidence is provided that a nanocrystalline and stacking-disordered, chemically stabilized β-cristobalite form of AlPO4 occurs in a sewage sludge ash (SSA). This proof is based on a combined X-ray powder diffraction and X-ray fluorescence investigation of an SSA produced at a large-scale fluidized bed incineration facility serving a catching area with a population of 2 million. The structural and chemical characterization was carried out on 'as received' SSA samples as well as on solid residues remaining after leaching this SSA in sodium hydroxide solution. Thus, it was ascertained that the observed nanocrystalline and stacking-disordered cristobalite-like component belongs to the aluminum phosphate component of this SSA, rather than to its silicon dioxide component. In addition, a direct proof is presented that the chemically stabilized β-cristobalite form of AlPO4 does crystallize from X-ray amorphous precursors under conditions that mimic the huge heating rate and short retention time (just seconds at T ≈ 850°C), typical for fluidized bed incinerators. KW - Aluminum phosphate KW - Chemical stabilization of high-temperature forms KW - Cristobalite form KW - Stacking disorder KW - Incinerator ash KW - Sewage sludge ash PY - 2015 DO - https://doi.org/10.1017/S0885715614001213 SN - 0885-7156 VL - 30 IS - Supplement S 1 SP - S31 EP - S35 PB - JCPDS CY - Swarthmore, Pa. AN - OPUS4-33435 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schraut, Katharina A1 - Adamczyk, Burkart A1 - Adam, Christian A1 - Stephan, D. A1 - Meng, Birgit A1 - Simon, Sebastian A1 - von Werder, Julia T1 - Synthesis and characterisation of alites from reduced basic oxygen furnace slags N2 - Basic oxygen furnace slags (BOFS) are by-products of the steelmaking process. Several researchers have studied the production of Portland cement clinker and metallic iron from BOFS via a reductive treatment. In this study, we applied a carbothermal reduction of BOFS in a technical-scale electric arc furnace and characterised the clinker-like products. Those clinker-like non-metallic products (NMPs) had a chemical and mineralogical composition comparable to clinker for ordinary Portland cement (OPC) and contained large elongated alite crystals as major component. The pure NMPs reacted more slowly and achieved a lower degree of hydration compared with commercial OPC. If the reactivity of the products can be further increased by employing specific adaptations, it can be used as a full clinker substitute for OPC. Nevertheless, it is also an option to use the material without further modifications as a cement component or concrete addition, which contributes to the strength development in both cases. KW - BOFS KW - Hydration products KW - Thermal analysis KW - X-ray diffraction PY - 2021 DO - https://doi.org/10.1016/j.cemconres.2021.106518 SN - 0008-8846 VL - 147 SP - 6518 PB - Elsevier Ltd. AN - OPUS4-52939 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Raniro, H.R. A1 - Teles, A.P. A1 - Pavinato, P.S. A1 - Adam, Christian T1 - Phosphorus solubility and dynamics in a tropical soil under sources derived from wastewater and sewage sludge N2 - Conventional phosphate fertilizers are usually highly water-soluble and rapidly solubilize when moistened by the soil solution. However, if this solubilization is not in alignment with plants demand, P can react with the soil colloidal phase, becoming less available over time. This is more pronounced in acidic, oxidic tropical soils, with high P adsorption capacity, reducing the efficiency of P fertilization. Furthermore, these fertilizers are derived from phosphate rock, a non-renewable resource, generating an environmental impact. To assess these concerns, waste-recycled P sources (struvite, hazenite and AshDec®) were studied for their potential of reducing P Fixation by the soil and improving the agronomic efficiency of the P fertilization. In our work, we compared the solubilization dynamics of struvite, hazenite, AshDec® to triple superphosphate (TSP) in a sandy clay loam Ferralsol, as well as their effect on solution pH and on soil P pools (labile, moderately-labile and non-labile) via an incubation experiment. Leaching columns containing 50 g of soil with surface application of 100 mg per column (mg col􀀀 1) of P from each selected fertilizer and one control (nil-P) were evaluated for 60 days. Daily leachate samples from the column were analyzed for P content and pH. Soil was stratified in the end and submitted to P fractionation. All results were analyzed considering p < 0.05. Our findings showed that TSP and struvite promoted an acid P release reaction (reaching pHs of 4.3 and 5.5 respectively), while AshDec® and hazenite reaction was alkaline (reaching pHs of 8.4 and 8.5 respectively). Furthermore, TSP promoted the highest P release among all sources in 60 days (52.8 mg col􀀀 1) and showed rapid release dynamic in the beginning, while struvite and hazenite showed late release dynamics and lower total leached P (29.7 and 15.5 mg col􀀀 1 P respectively). In contrast, no P-release was detected in the leachate of the AshDec® over the whole trial period. Struvite promoted the highest soil labile P concentration (7938 mg kg􀀀 1), followed by hazenite (5877 mg kg􀀀 1) and AshDec® (4468 mg kg􀀀 1), all higher than TSP (3821 mg kg􀀀 1), while AshDec® showed high moderately-labile P (9214 mg kg􀀀 1), reaffirming its delayed release potential. KW - Phosphate dynamics KW - Struvite KW - Wastewater KW - Sewage sludge ash KW - CaNaPO4 KW - P speciation PY - 2022 DO - https://doi.org/10.1016/j.jenvman.2021.113984 VL - 302 IS - Part A SP - 113984 PB - Elsevier Ltd. AN - OPUS4-53600 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Adam, Christian A1 - Kley, Gerd A1 - Simon, Franz-Georg T1 - Thermal treatment of municipal sewage sludge aiming at marketable P-fertilisers N2 - Municipal sewage sludge is a carrier of nutrients – most important phosphorus (P) – but also contains organic pollutants and heavy metals. A two steps thermal treatment is suggested based on 1. mono-incineration of sewage sludge under destruction of organic pollutants and 2. thermochemical treatment of the resulting ashes to remove heavy metals and increase P-bioavailability. The targeted products are marketable P-fertilisers. The thermochemical treatment was investigated in a gas tight lab-scale rotary furnace. Seven sewage sludge ashes of different origin and composition and one residue from gasification of sewage sludge were mixed with a chlorine donor (e.g. MgCl2) and thermochemically treated under systematic variation of operational parameters. The distributions of the heavy metals between solid and gas phase were determined. The heavy metals concentrations of the treated ashes met the legislative limits in most cases. The products from thermochemical treatment are suited raw materials for P-fertiliser production. Relevant process parameters such as temperature, type and concentration of Cl-donor and retention time were optimised for the thermochemical treatment step. KW - Sewage sludge KW - Mono-incineration KW - Ash treatment KW - Thermochemical treatment KW - Phosphorus-fertiliser PY - 2007 SN - 1345-9678 SN - 1347-5320 VL - 48 IS - 12 SP - 3056 EP - 3061 PB - Japan Institute of Metals CY - Sendai AN - OPUS4-16647 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Herzel, Hannes A1 - Krüger, Oliver A1 - Hermann, L. A1 - Adam, Christian T1 - Sewage sludge ash - A promising secondary phosphorus source for fertilizer production N2 - 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. KW - Sewage sludge ash KW - Phosphorus recovery KW - Thermochemical treatment KW - Reducing conditions KW - Heavy metal evaporation KW - Bioavailability KW - Sodium sulfate PY - 2016 DO - https://doi.org/10.1016/j.scitotenv.2015.08.059 SN - 0048-9697 SN - 1879-1026 IS - 542 SP - 1136 EP - 1143 PB - Elsevier CY - Amsterdam AN - OPUS4-34165 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Adam, Christian A1 - Peplinski, Burkhard A1 - Michaelis, Matthias A1 - Kley, Gerd A1 - Simon, Franz-Georg T1 - Thermochemical treatment of sewage sludge ashes for phosphorus recovery N2 - Phosphorus (P) is an essential element for all living organisms and cannot be replaced. Municipal sewage sludge is a carrier of phosphorus, but also contains organic pollutants and heavy metals. A two-step thermal treatment is suggested, including mono-incineration of sewage sludge and subsequent thermochemical treatment of the ashes. Organic pollutants are completely destroyed by mono-incineration. The resulting sewage sludge ashes contain P, but also heavy metals. P in the ashes exhibits low bioavailability, a disadvantage in farming. Therefore, in a second thermochemical step, P is transferred into mineral phases available for plants, and heavy metals are removed as well. The thermochemical treatment was investigated in a laboratory-scale rotary furnace by treating seven different sewage sludge ashes under systematic variation of operational parameters. Heavy metal removal and the increase of the P-bioavailability were the focus of the investigation. The present experimental study shows that these objectives have been achieved with the proposed process. The P-bioavailability was significantly increased due to the formation of new mineral phases such as chlorapatite, farringtonite and stanfieldite during thermochemical treatment. KW - P-recovery KW - Sewage sludge ash KW - Thermochemical treatment KW - Mineral phases KW - X-ray diffraction PY - 2009 DO - https://doi.org/10.1016/j.wasman.2008.09.011 SN - 0956-053X VL - 29 IS - 3 SP - 1122 EP - 1128 PB - Pergamon Press CY - New York, NY AN - OPUS4-18605 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Ante, A. A1 - Trumpler, A. A1 - Niermann, S. A1 - Decker, Renate A1 - Hermann, L. A1 - Adam, Christian T1 - SUSAN - Sustainable and safe re-use of municipal sewage sludge for nutrient recovery KW - Sewage sludge KW - Phosphorus KW - Recycling KW - Thermochemical treatment KW - Heavy metal removal KW - Large scale consideration PY - 2010 SN - 0016-3651 VL - 151 IS - 13 SP - 78 EP - 84 PB - Oldenbourg-Industrieverl. CY - München AN - OPUS4-22097 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Hobohm, J. A1 - Kuchta, K. A1 - Krüger, Oliver A1 - van Wasen, Sebastian A1 - Adam, Christian T1 - Optimized elemental analysis of fluorescence lamp shredder waste N2 - 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). KW - Yttrium KW - Rare earth elements KW - Elemental analysis KW - Microwave-assisted digestion PY - 2016 DO - https://doi.org/10.1016/j.talanta.2015.09.068 SN - 0039-9140 VL - 147 SP - 615 EP - 620 PB - Elsevier CY - Amsterdam AN - OPUS4-34992 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Stemann, Jan A1 - Peplinski, Burkhard A1 - Adam, Christian T1 - Thermochemical treatment of sewage sludge ash with sodium salt additives for phosphorus fertilizer production - Analysis of underlying chemical reactions N2 - Stocks of high grade phosphate rock are becoming scarce, and there is growing concern about potentially harmful impurities in conventional phosphorus fertilizers. Sewage sludge ash is a promising secondary phosphorus source. However, to remove heavy metals and convert the phosphorus contained in sewage sludge ash into mineral phases available to plants, an after-treatment is required. Laboratory-scale calcination experiments of sewage sludge ash blended with sodium salts using dried sewage sludge as a reducing agent were carried out at 1000 °C. Thus, the Ca3(PO4)2 or whitlockite component of raw sewage sludge ash, which is not readily plant available, was converted to CaNaPO4 (buchwaldite). Consequently, nearly complete phosphorus solubility in ammonium citrate (a well-established indicator for plant availability) was achieved. Moreover, it was shown that Na2CO3 may be replaced by moderately priced Na2SO4. However, molar ratios of Na/P > 2 were required to achieve >80% phosphorus solubility. Such over-stoichiometric Na consumption is largely caused by side reactions with the SiO2 component of the sewage sludge ash – an explanation for which clear evidence is provided for the first time. KW - Phosphorus recovery KW - Plant availability KW - Solubility in ammonium citrate KW - Whitlockite-to-buchwaldite transformation PY - 2015 DO - https://doi.org/10.1016/j.wasman.2015.07.029 SN - 0956-053X VL - 45 SP - 385 EP - 390 PB - Pergamon Press CY - New York, NY AN - OPUS4-33876 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -