TY - JOUR A1 - Stößer, R. A1 - Feist, M. A1 - Willgeroth, Carola A1 - Emmerling, Franziska A1 - Menzel, Michael A1 - Reuther, H. T1 - The 'quiet Goldschmidt' - a mechanochemical, thermoanalytical, and spectroscopic study of selected steps of the aluminothermic reaction N2 - The Goldschmidt reaction (2Al+α-Fe2O3) was investigated both under mechanical and thermal activation by employing a combination of analytical methods such as ESR and Mössbauer spectroscopy, magnetic susceptibility, X-ray powder diffraction, and thermal analysis (TA). Both the mechanical treatment and the TA runs under air caused the reaction conditions of 'quiet redox reactions' due to a retarding effect and enabled a reaction study in a 'slow motion mode'. This allowed to establish distinct partial steps of the integral reaction process depending on the intensity of the mechanical impact, the educt composition, the gas phase composition, and, finally, the thermal excitation in the TA runs. Particular attention was payed to the role of the gas phase and to the reaction of aluminum with differently activated oxygen species. The phlegmatizing effect was traced back to the formation of Al2O3 coverages of the Al particles. KW - Thermite reaction KW - Iron ESR and Mössbauer spectroscopy KW - Mechanochemical activation KW - Magnetic moments KW - DTA-TG KW - XRD PY - 2013 U6 - https://doi.org/10.1016/j.jssc.2013.02.032 SN - 0022-4596 SN - 1095-726X VL - 202 SP - 173 EP - 190 PB - Elsevier CY - San Diego, Calif. AN - OPUS4-29528 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Stößer, R. A1 - Feist, M. A1 - Patzwaldt, K. A1 - Menzel, Michael A1 - Emmerling, Franziska ED - Brooks, H. T1 - Redox reactions of K3[Fe(CN)6] during mechanochemically stimulated phase transitions of AlOOH N2 - Thermally induced redox reactions of K3[Fe(CN)6] (1) were investigated for a broad temperature range by thermal methods and structure analytical methods (ESR and Mößbauer spectroscopy, X-ray Powder diffraction and XANES). Based on the influence of the mechanically activated and transforming matrices 2 and 3, redox processes can be tuned to form doped Al2O3 systems which contain either isolated Fe3+ centres or redox active phases and precursors like (Al1-xFex)2O3 (4), (Al3-xFex)O4 (5), Fe3O4, Fe2O3 and Fe0. The phase Fe3C and the chemically reactive C-species were detected during the reaction of 1. The final composition of the doped products of α-Al2O3 is mainly influenced by the chemical nature of the Fe doping component, the applied temperature and time regime, and the composition of the gas phase (N2, N2/O2 or N2/H2). From the solid state chemistry point of view it is interesting that the transforming matrix (2 and 3) possesses both oxidative and protective properties and that the incorporation of the Fe species can be performed systematically. KW - A. Inorganic compounds KW - C. Mössbauer spectroscopy KW - C. Thermogravimetric analysis KW - D. Electron paramagnetic resonance KW - ESR-Spektroskopie KW - Kaliumhexacyanoferrat(III) KW - Mechanische Aktivierung KW - Mößbauer-Spektroskopie KW - Redoxreaktionen KW - TA-MS-Messungen PY - 2011 U6 - https://doi.org/10.1016/j.jpcs.2011.03.016 SN - 0022-3697 VL - 72 IS - 6 SP - 794 EP - 799 PB - Pergamon Press CY - New York, NY AN - OPUS4-23685 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Jung, S. A1 - Renz, F. A1 - Klein, M. A1 - Menzel, Michael A1 - Boca, R. A1 - Stößer, R. T1 - Molecular switching in iron complexes bridged via tincyanides observed by Mössbauer and ESR spectroscopy N2 - The precursor [FeIII(L)Cl] (LH2 = N,N'-bis(2'-hydroxy-3'-X-benzyliden)-1,6-diamino-3-N-hexane) is a high-spin (S = 5/2) complex (with X = -CH3, -O-CH3). This precursor is combined with the bridging unit [SnIV(CN)4] to yield star-shaped pentanuclear clusters, [(L-X-FeIII)4Sn(CN)4]Cl4 57Fe-Mössbauer, 119mSn-Mössbauer, and ESR spectroscopy are used to study our samples. For X = -CH3 the 57Fe-Mössbauer data show a multiple spin transition between iron(III) in the high-spin and low-spin state. Changing the functional group from X = -CH3 to X = -O-CH3 turns the switchability off. KW - Switching iron complexes KW - Spin-transition KW - Mössbauer spectroscopy KW - ESR-spectroscopy PY - 2010 U6 - https://doi.org/10.1088/1742-6596/217/1/012027 SN - 1742-6588 SN - 1742-6596 VL - 217 IS - 1 / 012027 SP - 1 EP - 6 PB - IOP Publ. CY - Bristol, UK AN - OPUS4-22561 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Stößer, R. A1 - Menzel, Michael A1 - Feist, M. A1 - Nofz, Marianne A1 - Renz, F. T1 - Competing redox reactions in Fe-containing AlO(OH) and Al2O3 matrices: A combined investigation by Mössbauer, ESR spectroscopy and thermal analysis N2 - The investigation of iron-doped AlO(OH)/Al2O3 systems revealed that the combined employment of Mössbauer and ESR spectroscopies together with thermal analysis yields meaningful data with complementary information. This mutual complementarity is based on the coexistence of Fe point defects with the corresponding aggregated FeOx species which has been observed even for very low Fe concentrations. Competing redox processes between the dopant, the AlOx matrix, and the gas atmosphere during the thermal treatment enable the generation of solid phases exhibiting specific chemical properties. The entire reaction process is influenced by a specific mechanical and thermal pre-treatment that affects predominantly oxydative processes in the matrix. A protecting influence of the matrix preventing further reductive attack of the Fe3+ Fe2+ ions by hydrogen has been established. KW - Mössbauer KW - ESR spectroscopy KW - Thermal analysis KW - Al2O3 KW - Magnetite KW - Fe(0) KW - Fe(2+) KW - Fe(3+) PY - 2010 UR - http://iopscience.iop.org/1742-6596/217/1/012028/pdf/1742-6596_217_1_012028.pdf U6 - https://doi.org/10.1088/1742-6596/217/1/012028 SN - 1742-6588 SN - 1742-6596 VL - 217 IS - 1 SP - 012028-1 - 012028-5 PB - IOP Publ. CY - Bristol, UK AN - OPUS4-21876 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Stößer, R. A1 - Feist, M. A1 - Menzel, Michael A1 - Nofz, Marianne T1 - Fe3+ ions acting as probes and agents in aggregation processes and solid-state reactions in AlO(OH)/Al2O3 matrices N2 - The fate of doped iron species during various mechanically and thermally initiated redox reactions and aggregation processes in crystalline and amorphous AlO(OH) or Al2O3 matrices was investigated. The amorphization of the matrix was performed by chemical (i.e., via sol-gel processes) or mechanochemical treatment (high-energy ball milling). Thermal analysis, coupled with mass spectrometry (TA-MS), Mössbauer spectroscopy, and electron spin resonance (ESR), was used. The TA under various gas atmospheres allowed preparing samples under a controlled temperature regime, together with a controlled gas influence. Both the effect of mechanical activation and the influence of the iron doping could be followed macroscopically via the down-shift of the peak temperature of the corundum formation. The ESR data characterize the Fe3+ ions and their interaction with the magnetic surrounding based on the fine structure parameters. The Mössbauer data allowed the characterization of the Fe(0), Fe2+, and Fe3+ species, together with providing information about their coordinative surrounding. Both methods provided general complementary spectroscopical information. Unexpectedly, (FeOx)n and (FexAl1-x)2O3 aggregates could also be detected in the range of low Fe concentrations. It was demonstrated that even in the low-level doped systems [(FexAl1-x)2O3 with x ≥ 0.01], all the essential spectroscopic phenomena occur. At higher Fe concentrations, they were discovered to be caused by magnetic and spin exchange interactions as well as by solid-state reactions during and after the mechanical activation. PY - 2010 U6 - https://doi.org/10.1111/j.1551-2916.2009.03596.x SN - 0002-7820 SN - 1551-2916 VL - 93 IS - 5 SP - 1447 EP - 1456 PB - Blackwell Publishing CY - Malden AN - OPUS4-21235 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Stößer, R. A1 - Menzel, Michael A1 - Feist, M. T1 - The fate of Fe3+ ions in the system {AlO(OH)-xerogel/Fe-compounds} after mechanical activation and different thermal treatments studied by Mössbauer, ESR spectroscopy and thermal analysis KW - Mössbauer KW - ESR KW - Thermal analysis KW - High energy ball milling KW - Activation/deactivation processes KW - Local mechano-chemical reactions KW - Heterogeneous redox reactions PY - 2009 U6 - https://doi.org/10.1007/s10751-009-9920-0 SN - 0304-3843 SN - 1572-9540 VL - 190 IS - 1-3 SP - 43 EP - 49 PB - Kluwer CY - Dordrecht AN - OPUS4-19478 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - GEN A1 - Stößer, R. A1 - Brenneis, Rudolf A1 - Herrmann, Werner A1 - Steinfeldt, N. ED - Petzow, G. T1 - Nachweis mechanisch induzierter Strukturänderungen bei Druck- bzw. Biegebelastung hochkorundhaltiger Werkstoffe mit Hilfe der Elektronenspinresonanz T2 - Beiträge zum Abschlußkolloquium im Schwerpunktprogramm "Keramische Hochleistungswerkstoffe" der Deutschen Forschungsgemeinschaft CY - Stuttgart, Deutschland DA - 1994-02-17 PY - 1996 SN - 3-527-27138-4 SP - 287 EP - 297 PB - VCH CY - Weinheim AN - OPUS4-12653 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Stößer, R. A1 - Nofz, Marianne A1 - Feist, M. A1 - Scholz, G. T1 - Fe3+-assisted formation of alpha-Al2O3, starting from sol-gel precursors N2 - The role of Fe3+ ions in the transformations from boehmites and pseudoboehmite xerogels via transition aluminas to corundum was studied here. Especially, the active iron species responsible for the decrease of the temperature of transformation to corundum were looked for. To enable the formation of various Fe3+ and Fe2+ species, samples were subjected to thermal treatments in different atmospheres as well as mechanically activated. Thermal analysis and ESR spectroscopy served to follow the processes and to characterise the resulting products. It was found that (i) isolated Fe3+ ions can indicate local structural changes but have (almost) no influence on the temperature of corundum formation, (ii) the temperature of corundum formation decreases in the result of action of small α-Fe2O3 particles and (iii) during thermal treatments Fe3+ ions are distributed between different phases or precursors thereof: transition aluminas, corundum, Fe2O3, and a Fe3+ pool. KW - Redox process KW - ESR spectroscopy KW - Thermal analysis KW - Sol-gel process KW - Boehmite KW - Corundum PY - 2006 U6 - https://doi.org/10.1016/j.jssc.2005.11.026 SN - 0022-4596 SN - 1095-726X VL - 179 IS - 3 SP - 645 EP - 657 PB - Elsevier CY - San Diego, Calif. AN - OPUS4-11889 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mehner, Hartmut A1 - Feist, M. A1 - Stößer, R. A1 - Scholz, G. A1 - Kemnitz, E. A1 - Dwelk, H. T1 - Halogeno metallates of transition elements with cations of nitrogen-containing heterocyclic bases, IX. Moessbauer and ESR spectroscopic investigation of aquachloro- and bromoferrates(III). On the compatibility of structural information obtained by spectroscopic and diffraction methods N2 - The 57Fe-Moessbauer spectrum of (dmpipzH2)2[FeIII(H2O)2Cl4][FeIII Cl4]Cl2 (1) consists of two doublets caused by a strongly distorted octahedral and a non-distorted tetrahedral component. Both (dmpipzH2)[FeIIIBr4]2 (2) and (trienH2)[FeIIIBr4]Br (3) show only one doublet indicating a more strongly distorted iron(III) species for 2 and a less-distorted one in the case of 3. For all compounds investigated, the ESR spectra reveal the existence of ground states with predominant antiferromagnetic coupling. The Néel temperatures amount to <4.2 K for 1, 4 K for 3 and 48 K for 2. In the case of 2, both the Moessbauer and the ESR spectra reveal the formation of exchange-coupled {FeBr4} units which has been attributed to a significant cation influence. The fine structure of residual paramagnetic [FeBr4]- subunits remaining in the crystalline matrix could be directly determined. Temperature dependent AC and DC susceptibility measurements of 2 and 3 confirmed the results. KW - Iron coordination KW - Antiferromagnetic coupling KW - Exchange-coupled units KW - ESR fine structure KW - Magnetic susceptibility PY - 2002 U6 - https://doi.org/10.1016/S1293-2558(01)01193-1 SN - 1293-2558 SN - 1873-3085 VL - 4 IS - 1 SP - 109 EP - 115 PB - Elsevier CY - Amsterdam AN - OPUS4-1311 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nofz, Marianne A1 - Bartoll, Jens A1 - Stößer, R. T1 - Complementarity of ESR and optical absorption of gamma-irrradiated silicate glasses N2 - Radiation defects in alkaline earth silicate glasses are studied by means of ESR and optical spectroscopies. Previously undiscovered relations between findings of both methods are deduced using four different experimental tools: (i) variation of chemical glass composition; (ii) isochronal annealing of ggr-irradiated samples; (iii) optical bleaching of ggr-irradiated samples; (iv) variation of the ggr-dose. Oxygen hole centres are mainly responsible for the radiation induced absorption in the visible part of the optical spectrum. Previously undescribed electron centres with broad and asymmetric ESR resonances (gprime=1·955) contribute to the optical spectra (200–2000 nm) in a small way. It is suggested they are electrons trapped on small aggregates of alkaline earth ions. The radiation induced recharging of incorporated Fe3+ ions is also evidenced by optical and ESR spectroscopies. Fe3+ ions react as electron traps forming not only Fe2+ but also {Fe3+}- species which might be responsible for an absorption band at 300 nm. A correlation was found between the changes of intensity with those of the ESR spectroscopically detected Fe3+ content of the samples. PY - 2000 UR - http://www.ingentaconnect.com/content/sgt/pcg/2000/00000041/00000003/4103140 SN - 0031-9090 VL - 41 IS - 3 SP - 140 EP - 149 PB - Thornton CY - Sheffield AN - OPUS4-938 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Bartoll, Jens A1 - Nofz, Marianne A1 - Stößer, R. T1 - Generation and conversion of electronic defects in calcium carbonates by UV/Vis light N2 - Radical species like CO-2,CO-3, SO-2, and SO-3 can be created by exposing natural and synthetic calcium carbonates to sunlight or to the light of a Hg(Xe) lamp. This poses as a risk for ESR dating of these materials, because the radicals formed by light exposure cannot be distinguished from those generated by radioactivity. Furthermore, paramagnetic centers like SO-2, electrons trapped near Zn2+ or Cd2+ ions, surface defects, and radicals with g?=2.0040, can be bleached in ?-irradiated samples by light and show conversion effects. KW - ESR PY - 2000 U6 - https://doi.org/10.1016/S0969-8043(00)00044-0 SN - 0883-2889 SN - 0969-8043 IS - 52 SP - 1099 EP - 1105 PB - Elsevier CY - Amsterdam AN - OPUS4-892 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nofz, Marianne A1 - Stößer, R. A1 - Sebastian, S. A1 - Scholz, G. A1 - Willer, M. A1 - Jeschke, G. A1 - Schweiger, A. T1 - Pulse EPR Spectroscopy of Cu2+ - Doped Inorganic Glasses KW - EPR Spectroscopy KW - Inorganic glasses PY - 1999 SN - 0937-9347 SN - 1613-7507 IS - 16 SP - 507 EP - 528 PB - Springer CY - Wien AN - OPUS4-760 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Nofz, Marianne A1 - Reich, Christian A1 - Stößer, R. A1 - Bartoll, Jens A1 - Janata, E. T1 - On the interaction of glasses with high-energy radiation - Combined ESR and optical studies T2 - 71st Annual Meeting of the German Society of Glass Technology (DGG) CY - Bayreuth, Germany DA - 1997-05-01 KW - Glas KW - Glaskeramik KW - Optical spectroscopy PY - 1999 SN - 0946-7475 VL - 72 IS - 3 SP - 76 EP - 90 PB - Verl. d. Dt. Glastechn. Ges. CY - Offenbach AN - OPUS4-758 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Mehner, Hartmut A1 - Zakharchuk, N. F. A1 - Stößer, R. A1 - Schroder, U. A1 - Scholz, F. T1 - Solid state electrochemistry, X-ray powder diffraction, magnetic susceptibility, electron spin resonance, Mössbauer and diffuse reflectance spectroscopy of mixed iron(III)-cadmium(II) hexacyanoferrates KW - Festkörper KW - Elektrochemie KW - Mössbauer KW - Suszeptibilität KW - Magnetisierungskoeffizient PY - 1999 SN - 1432-8488 SN - 1433-0768 IS - 3 SP - 264 EP - 276 PB - Springer CY - Berlin AN - OPUS4-713 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -