TY - JOUR A1 - Müller, Ralf A1 - Meszaros, Robert A1 - Peplinski, Burkhard A1 - Reinsch, Stefan A1 - Eberstein, Markus A1 - Schiller, Wolfgang Arno A1 - Deubener, J. T1 - Dissolution of alumina, sintering, and crystallization in glass ceramic composites for LTCC KW - LTCC KW - Sintering KW - Crystallization KW - Alumina dissolution KW - Rietveld analysis PY - 2009 DO - https://doi.org/10.1111/j.1551-2916.2009.03089.x SN - 0002-7820 SN - 1551-2916 VL - 92 IS - 8 SP - 1703 EP - 1708 PB - Blackwell Publishing CY - Malden AN - OPUS4-20676 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Peplinski, Burkhard A1 - Müller, Ralf A1 - Wenzel, Klaus-Jürgen A1 - Sojref, Regine A1 - Schultze, Dietrich ED - Delhez, R. T1 - An X-ray powder diffration investigation of a fine-grained synthetic a-cordierite powder T2 - 6th European Powder Diffraction Conference CY - Budapest, Hungary DA - 1998-08-22 KW - Alpha-cordierite KW - Indialite KW - Standard material KW - Back-filling specimen mount technique PY - 2000 SN - 0-87849-847-8 SN - 0255-5476 SP - 150 EP - 155 PB - Trans Tech Publ. CY - Uetikon-Zürich AN - OPUS4-1195 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Peplinski, Burkhard A1 - Feldmann, Ines A1 - Adam, Karin T1 - Können 5 ng oder 30 ng/g einer Nebenphase das Diffraktogramm einer Pulverprobe signifikant verändern? T2 - Gemeinsame Jahrestagung der Deutschen Gesellschaft für Kristallographie e. V. und der Deutschen Gesellschaft für Kristallwachstum und Kristallzüchtung e. V. CY - Jena DA - 2004-03-15 PY - 2004 SN - 0930-486X SP - 109 PB - Oldenbourg CY - München AN - OPUS4-3432 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Peplinski, Burkhard T1 - Können 5 ng oder 30 ng/g einer Nebenphase das Diffraktogramm einer Pulverprobe signifikant verändern? T2 - Tag der Chemie, Freie Universität Berlin CY - Berlin, Germany DA - 2005-06-08 PY - 2005 AN - OPUS4-7584 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Peplinski, Burkhard A1 - Adam, Christian T1 - A comparative study of commercial sewage sludge ashes (SSA) produced at HVC (DRSH) and SNB and of well defined model substances synthesized at BAM by X-ray powder diffraction (XRD) and other analytical techniques (ICP, XRF, SEM & EDX, Mossbauer spectroscopy, 27Al- and 31P solid state NMR) T2 - Meeting mit Industriepartnern des EU-Projekts SUSYPHOS/ Eurostar CY - Dordrecht, Netherlands DA - 2010-06-24 PY - 2010 AN - OPUS4-22445 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Peplinski, Burkhard T1 - First identification of AIPO4 tridymite in a municipal sewage sludge ash T2 - 12. European Powder Diffracion Conference (EPDIC-12) CY - Darmstadt, Germany DA - 2010-08-27 PY - 2010 AN - OPUS4-21968 LA - deu 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 - TY - CONF A1 - Peplinski, Burkhard T1 - Glimpses at individual reaction steps accompanying the crystallization of the tridmite form(s) of AIPO4 from an X-ray amorphous precipitate doped with potassium and magnesium T2 - Joint Meeting German Crystallographic Society (DKG), German Mineralogical Society (DMG) & Austrian Mineralogical Society (ÖMG) CY - Salzburg, Austria DA - 2011-09-20 PY - 2011 AN - OPUS4-24219 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Peplinski, Burkhard T1 - Nanocrystalline and stacking-disordered beta-cristobalite AlPO4 stabilized at room temperature: synthesis and X-ray powder diffraction data N2 - X-ray powder diffraction (XRD) patterns of the high-temperature (HT) cristobalite form of SiO2 and its isoelectronic AlPO4 analogue are essentially influenced by the dynamic disorder of these crystal structures. The nature of this disorder and of the phase transition between the α- and β-form has been the subject of intensive research during the last four decades [1]. By 1989 it became possible to stabilize the HT-form of cristobalite SiO2 at room temperature in laboratory and engineering ceramic industries by applying solid solution forming techniques [2]. However, for the HT-form of cristobalite AlPO4 nothing similar has been known until 2014 when it was discovered that nanocrystalline and stacking-disordered β-cristobalite AlPO4 is the major component of the fly ash of a large incineration facility operated by the waste water treatment authorities of Frankfurt/M. [3]. Previous comprehensive investigations of this fly ash failed to interpret its complex XRD pattern – presumably mainly due to the lack of a matching experimental digital pattern in the Powder Diffraction Database. The present paper reports on a synthesis route that facilitates the crystallization of nanocrystalline and stacking-disordered β-cristobalite AlPO4 that is free of crystalline impurity phases and long-term stable at ambient. Its room temperature XRD pattern is presented with parameters traced back to certified reference materials. [1] Yuan F. and Huang L., Phys. Rev, B, 2012, 85, 134114. [2] Perrotta J.A., Grubbs D.K., Martin E.S., Dando N.R., McKinstry H.A. and Huang C.-Y., J. Am. Ceram. Soc., 1989, 72, 441. [3] Peplinski B., Adam C., Adamczyk B., Müller R., Michaelis M., Krahl Th. and Emmerling F., Powder Diffraction Journal, 2015, 30, 2, Supp. 1, S31. T2 - 15. European Powder Diffraction Conference (EPDIC15) CY - Bari, Italy DA - 12. June 2016 KW - Stabilization of HT-structures at room temperature KW - β-cristobalite structure type KW - Databases PY - 2016 AN - OPUS4-36727 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Peplinski, Burkhard T1 - On the fast crystallization of the tridymite form of doped AlPO4 from a mixture of amorphous and crystalline precursor components and the chemical stabilization of its hexagonal high-temperature form at room temperature T2 - 88th Annual Meeting of the German Mineralogical Society CY - Münster, Germany DA - 2010-09-18 PY - 2010 AN - OPUS4-22448 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Adolphs, Jürgen A1 - Rübner, Katrin A1 - Schnell, A. A1 - Prinz, Carsten A1 - Peplinski, Burkhard A1 - Hempel, S. ED - Ludwig, H.-M. T1 - Porenstruktur hydrothermal erhärteter Granulate aus Mauerwerkbruch N2 - Die Herstellung hydrothermal erhärteter Granulate ist eine Möglichkeit zur Wiederverwertung von ziegelhaltigem Mauerwerkbruch, der derzeit aufgrund der heterogenen Zusammensetzung und hoher Feinanteile ein besonders hohes Verwertungsdefizit aufweist. Dabei ist die hydrothermale Erhärtung in einem Autoklav bei 200 °C und 1.6 MPa in gesättigter Wasserdampfatmosphäre eine Alternative mit geringerem Energieverbrauch im Vergleich zur thermischen Herstellung von Leichtgranulaten aus mineralischen Abfällen (Blähgranulate) oder Tonen und Schiefer (kommerzieller Blähton bzw. Blähschiefer), die bei Temperaturen von 1200-1300 °C im Drehrohrofen erfolgt. Die Festigkeit der Hydrothermalgranulate entwickelt sich bei diesem Prozess durch die Ausbildung von Calciumsilicathydrat-Phasen (CSH), die durch die Reaktion zwischen Quarzpartikeln und hydratisiertem Kalk entstehen. Die so erzeugten Hydrothermalgranulate haben Rohdichten zwischen 1500 kg/m3 und 2000 kg/m3. Damit und auch durch andere Eigenschaften unterscheiden sie sich von den thermisch erhärteten Blähgranulaten bzw. Blähtonen. Ursache dafür ist letztendlich eine sehr unterschiedliche Gefüge- und Porenstruktur. Im vorliegenden Beitrag wird hauptsächlich über die Ergebnisse der Mikrostrukturuntersuchungen an Hydrothermalgranulaten zusammen mit ihren technologischen Eigenschaften, wie Kornfestigkeit, Rohdichte und Wasseraufnahme, berichtet. T2 - 19. Ibausil - Internationale Baustofftagung CY - Weimar, Germany DA - 16.09.2015 KW - Leichtgranulat KW - Mauerwerkbruch KW - Hydrothermale Herstellung KW - Mikrostruktur KW - Porenstruktur PY - 2015 SN - 978-3-00-050225-5 VL - 2 SP - 2-291 EP - 2-298 AN - OPUS4-34878 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Adam, Christian A1 - Peplinski, Burkhard A1 - Kley, Gerd A1 - Simon, Franz-Georg ED - Hilty, L. M. T1 - Thermo-chemical treatment of sewage sludge ashes aiming at marketable P-fertiliser products T2 - R'07 World Congress "Recovery of Materials and Energy for Resource Efficiency" CY - Davos, Switzerland DA - 2007-09-03 KW - P-recovery KW - Sewage sludge KW - Thermo-chemical treatment KW - Mineral phases KW - XRD PY - 2007 SN - 978-3-905594-49-2 SP - 14/1 EP - 14/7 PB - EMPA CY - Davos AN - OPUS4-16469 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 -