TY - JOUR A1 - Eschlböck-Fuchs, S. A1 - Demidov, Alexander A1 - Gornushkin, Igor B. A1 - Schmid, Thomas A1 - Rössler, R. A1 - Huber, N. A1 - Panne, Ulrich A1 - Pedarnig, J. D. T1 - Tomography of homogenized laser-induced plasma by Radon transform technique N2 - Tomography of a laser-induced plasma in air is performed by inverse Radon transform of angle-resolved plasma images. Plasmas were induced by single laser pulses (SP), double pulses (DP) in collinear geometry, and by a combination of single laser pulses with pulsed arc discharges (SP-AD). Images of plasmas on metallurgical steel slags were taken at delay times suitable for calibration-free laser-induced breakdown spectroscopy (CFLIBS). Delays ranged from few microseconds for SP and DP up to tens of microseconds for SP-AD excitation. The white-light and the spectrally resolved emissivity ε(x,y,z) was reconstructed for the three plasma excitation schemes. The electron number density Ne(x,y,z) and plasma temperature Te(x,y,z) were determined from Mg and Mn emission lines in reconstructed spectra employing the Saha-Boltzmann plot method. The SP plasma revealed strongly inhomogeneous emissivity and plasma temperature. Re-excitation of plasma by a second laser pulse (DP) and by an arc discharge (SP-AD) homogenized the plasma and reduced the spatial variation of ε and Te. The homogenization of a plasma is a promising approach to increase the accuracy of calibration-free LIBS analysis of complex materials. KW - Plasma tomography KW - Laser induced plasma KW - Radon transform technique KW - Laser induced breakdown spectroscopy (LIBS) KW - Steel slag KW - Calibration-free analysis PY - 2016 DO - https://doi.org/10.1016/j.sab.2016.07.007 VL - 123 SP - 59 EP - 67 PB - Elsevier B.V. AN - OPUS4-37452 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Dariz, P. A1 - Schmid, Thomas T1 - Phase composition and burning history of high-fired medieval gypsum mortars studied by Raman microspectroscopy N2 - The use of high-fired gypsum as binder for masonry and joint mortars or stuccowork in Central Europe in the Early and High Middle Ages was a regional specific as it depended on local gypsum deposits. The calcination technology possible at the time resulted in an assemblage of calcium sulphate phases dehydrated to different degrees and partly thermally damaged accessory minerals of the raw gypsum. Not hydrated clusters of firing products preserved in the binder matrix are a typical feature of such mortars. A novel Raman microspectroscopic approach, providing access to the burning history of individual anhydrite grains, was applied to samples from medieval South Tyrolean stucco decorations and sculptures. Beyond that, Raman microspectroscopy was employed for tracing and visualising pyrometamorphic reactions in natural impurities of the kiln run. In the discussed examples mineral thermometry indicates process temperatures above 800°C: the breakdown of magnesium-rich chlorite led to the formation of forsterite Mg2SiO4, while the thermal decomposition of dolomite CaMg(CO3)2 to periclase MgO and lime CaO yielded – after hydration and carbonation – magnesite MgCO3, CaCO3 polymorphs and magnesian calcite. Hydration of periclase in the mixed gypsum paste containing sulphate ions also resulted in magnesium sulphate hydrates, here identified in the form of hexahydrite MgSO4·6H2O. Lower burning temperatures left the accessory minerals in their pristine form, but can be traced by measuring the spectra of individual anhydrite crystals in grains of firing products and evaluating Raman band widths. Throughout the present study, calcination temperatures ranging from approx. 600°C to 900°C were determined. KW - High-fired gypsum mortar KW - Anhydrite KW - Dolomite KW - Forsterite KW - Raman microspectroscopy PY - 2019 DO - https://doi.org/10.1016/j.matchar.2019.03.013 VL - 151 SP - 292 EP - 301 PB - Elsevier Inc. AN - OPUS4-48102 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Sarhan, R. M. A1 - Koopman, W. A1 - Schuetz, R. A1 - Schmid, Thomas A1 - Liebig, F. A1 - Koetz, J. A1 - Bargheer, M. T1 - The importance of plasmonic heating for the plasmondriven photodimerization of 4-nitrothiophenol N2 - Metal nanoparticles form potent nanoreactors, driven by the optical generation of energetic electrons and nanoscale heat. The relative influence of these two factors on nanoscale chemistry is strongly debated. This article discusses the temperature dependence of the dimerization of 4-nitrothiophenol (4-NTP) into 4,4′-dimercaptoazobenzene (DMAB) adsorbed on gold nanoflowers by Surface-Enhanced Raman Scattering (SERS). Raman thermometry shows a significant optical heating of the particles. The ratio of the Stokes and the anti-Stokes Raman signal moreover demonstrates that the molecular temperature during the reaction rises beyond the average crystal lattice temperature of the plasmonic particles. The product bands have an even higher temperature than reactant bands, which suggests that the reaction proceeds preferentially at thermal hot spots. In addition, kinetic measurements of the reaction during external heating of the reaction environment yield a considerable rise of the reaction rate with temperature. Despite this significant heating effects, a comparison of SERS spectra recorded after heating the sample by an external heater to spectra recorded after prolonged illumination shows that the reaction is strictly photo-driven. While in both cases the temperature increase is comparable, the dimerization occurs only in the presence of light. Intensity dependent measurements at fixed temperatures confirm this finding. KW - Nanoparticles KW - Plasmonic heating KW - Raman spectroscopy PY - 2019 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-475140 DO - https://doi.org/10.1038/s41598-019-38627-2 SN - 2045-2322 VL - 9 IS - 1 SP - 3060, 1 EP - 8 PB - Nature Publishing Group AN - OPUS4-47514 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schmid, Thomas A1 - Dariz, P. ED - Ziemann, M. T1 - Raman band widths of anhydrite II reveal the burning history of high-fired medieval gypsum mortars N2 - The use of high-fired gypsum as binder for masonry and joint mortars or stuccowork in Central Europe in the Early and High Middle Ages was a regional specific as it depended on local gypsum deposits. The calcination technology possible at the time resulted in an assemblage of calcium sulphate phases dehydrated to different degrees and partly thermally damaged accessory minerals of the raw gypsum. Because of the absence of medieval textbooks, the observation of high-temperature, low-pressure mineral transformations and the correlation of phases coexisting in not hydrated binder relicts in the gypsum matrix to the mineralogy of the raw material and the burning conditions constitute the only source to the historical technological know-how. The CaSO4–H2O system consists of five crystalline phases, which can be discriminated by structural analysis methods, such as Raman spectroscopy, due to obvious differences in their spectroscopic data: gypsum (CaSO4 ⋅ 2 H2O), bassanite (hemihydrate, CaSO4 ⋅ ½ H2O), anhydrite III (CaSO4), anhydrite II (CaSO4), and anhydrite I (CaSO4). Only recently, it was possible to demonstrate that small spectroscopic variations exist also within the relatively large stability range of anhydrite II from approx. 180°C to 1180°C: all Raman bands narrow with increasing burning temperature applied in the synthesis from gypsum powder. The determination of band widths of down to 3 cm-1 and differences between them of a few tenths of a wavenumber is not a trivial task. Thus, this contribution discusses peak fitting and strategies for correction of instrument-dependent band broadening. Raman maps of polished thin sections of gypsum mortars provide access to the burning histories of individual remnant thermal anhydrite grains and enable the discrimination of natural anhydrite originating from the gypsum deposit. This novel analytical method was applied to samples from medieval South Tyrolean stucco decorations and sculptures. Beyond that, Raman microspectroscopy was employed for following pyrometamorphic reactions in natural impurities of the raw material. In the presented examples mineral thermometry indicates process temperatures above 800°C: the breakdown of magnesium-rich chlorite led to the formation of forsterite Mg2SiO4, while the thermal decomposition of dolomite CaMg(CO3)2 yielded – after hydration and carbonation – magnesite MgCO3, CaCO3 polymorphs and magnesian calcite. Lower burning temperatures, which leave the accessory minerals in their pristine form, can be traced by measuring the spectra of anhydrite crystalites in grains of firing products and evaluating Raman band widths. Throughout the applications of this analytical method so far, calcination temperatures ranging from approx. 600°C to 900°C were determined. T2 - 10th International Congress on the Application of Raman Spectroscopy in Art and Archaeology CY - Potsdam, Germany DA - 03.09.2019 KW - Raman microspectroscopy KW - High-fired medieval gypsum mortars KW - Raman band width KW - Gypsum dehydration KW - Thermal anhydrite PY - 2019 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-496204 SP - 36 EP - 37 PB - University of Potsdam CY - Potsdam AN - OPUS4-49620 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schmid, Thomas T1 - Research in the SALSA Application Lab – Shedding light onto high-fired medieval gypsum mortars N2 - After an introduction into the SALSA lab building and the ideas and sources of inspiration for building up the Application Lab as a spectroscopy lab with a strong focus on imaging and microspectroscopy, a very successful example of an interdisciplinary collaboration between the fields of art technology and analytical sciences is presented. T2 - Make and Measure 2019 CY - Berlin, Germany DA - 25.10.2019 KW - Interdisciplinary research KW - Teaching KW - High-fired medieval gypsum mortars KW - Raman spectroscopy PY - 2019 AN - OPUS4-49623 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schmid, Thomas T1 - Raman band widths of anhydrite II reveal the burning history of high‐fired medieval gypsum mortars N2 - An interdisciplinary collaboration between art technology and analytical sciences yielded an approach based on Raman microspectroscopy for the determination of the burning temperatures applied during the production process of high-fired medieval gypsum mortars. Analytical challenges and applications of the approach to examples from the cultural heritage of South Tyrol are presented. T2 - 10th International Congress on the Application of Raman Spectroscopy in Art and Archaeology CY - Potsdam, Germany DA - 03.09.2019 KW - Raman microspectroscopy KW - High-fired medieval gypsum mortars KW - Thermal anhydrite PY - 2019 AN - OPUS4-49624 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Riedel, Soraya A1 - Hülagü, Deniz A1 - Bennet, Francesca A1 - Carl, Peter A1 - Flemig, Sabine A1 - Schmid, Thomas A1 - Schenk, J. A. A1 - Hodoroaba, Vasile-Dan A1 - Schneider, Rudolf T1 - Electrochemical Immunomagnetic Ochratoxin A Sensing: Steps Forward in the Application of 3,3’,5,5’- Tetramethylbenzidine in Amperometric Assays N2 - Electrochemical methods offer great promise in meeting the demand for user-friendly on-site devices for Monitoring important parameters. The food industry often runs own lab procedures, for example, for mycotoxin analysis, but it is a major goal to simplify analysis, linking analytical methods with smart technologies. Enzyme-linked immunosorbent assays, with photometric detection of 3,3’,5,5’-tetramethylbenzidine (TMB),form a good basis for sensitive detection. To provide a straightforward approach for the miniaturization of the detectionstep, we have studied the pitfalls of the electrochemical TMB detection. By cyclic voltammetry it was found that the TMB electrochemistry is strongly dependent on the pH and the electrode material. A stable electrode response to TMB could be achieved at pH 1 on gold electrodes. We created a smartphonebased, electrochemical, immunomagnetic assay for the detection of ochratoxin A in real samples, providing a solid basis forsensing of further analytes. KW - Ochratoxin A KW - Amperometry KW - Cyclic voltammetry KW - Electrochemistry KW - Immunoassay PY - 2021 UR - https://nbn-resolving.org/urn:nbn:de:kobv:b43-530421 DO - https://doi.org/10.1002/celc.202100446 N1 - Geburtsname von Riedel, Soraya: Höfs, S. - Birth name of Riedel, Soraya: Höfs, S. VL - 8 IS - 13 SP - 2597 EP - 2606 AN - OPUS4-53042 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Schmid, Thomas A1 - Jungnickel, R. A1 - Dariz, P. T1 - Raman band widths of anhydrite II reveal the burning history of high‐fired medieval gypsum mortars N2 - When used as a mineral binder, gypsum is thermally dehydrated and mixed with water, resulting in a paste hardening in the backreaction to calcium sulphate dihydrate (CaSO4 · 2 H2O). Although nowadays mainly hemihydratebased (CaSO4 · ½ H2O) binders are employed, higher firing temperatures in medieval kilns yielded anhydrite II (CaSO4). Except for the discrimination of the metastable phases anhydrite III and I due to different crystal structures, variations within the production temperature range of anhydrite II (approximately 300 to 1180°C) were not analytically accessible until recently. This study describes the development of an analytical technique, which is based on steady changes of band widths in room‐temperature Raman spectra of anhydrite II as a function of burning temperature. Raman microspectroscopic mapping experiments enable to pinpoint individual unreacted grains of thermal anhydrite in mortars and to discriminate them from natural anhydrites originating from the raw gypsum. The determination of band full widths at half maximum of down to 3 cm−1 and differences between them of a few tenths of wavenumbers is not a trivial task. Thus, a focus of this work is on peak fitting and strategies for correction of instrument‐dependent band broadening, which is often neglected also beyond the field of mortar analysis. Including other potential influences on band widths, burning temperatures of 400 to 900°C can be retraced in high‐fired medieval gypsum mortars with an uncertainty of approximately ± 50 K, as demonstrated with sample material of a stucco sculpture dated around 1400. KW - Analytical methods KW - Gypsum dehydration KW - High-fired gypsum mortar KW - Raman band width determination KW - Thermal anhydrite PY - 2019 DO - https://doi.org/10.1002/jrs.5632 SN - 1097-4555 VL - 50 IS - 8 SP - 1154 EP - 1168 PB - Wiley AN - OPUS4-48757 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Schmid, Thomas T1 - Gips – ein unterschätztes Material N2 - Früh- bis spätmittelalterliche Stuckausstattungen bilden ein regionales, da an Gips-vorkommen korreliertes kunsttechnologisches Spezifikum. Aufgrund der beschränkten Kontrollmöglichkeiten über die in einem Meiler oder Feldofen herrschenden Parameter charakterisiert mittelalterliche Hochbrandgipse ein Phasengemisch aus Calciumsulfat-Hydratstufen und thermisch mehr oder weniger stark geschädigten Nebenbestandteilen aus der Gipslagerstätte. Die Analyse mittelalterlicher Hochbrandgipse erfordert die genaue Kenntnis der Bildungs- und Stabilitätsbereiche der Phasen im System CaSO4–H2O. Gips CaSO4 x 2 H2O entwässert beim Brennen über Halbhydrat CaSO4 x 0.5 H2O zu Anhydrit III CaSO4, welches schließlich in den für mittelalterliche Hochbrandgipse relevanten Anhydrit II (AII) übergeht. Für diesen wurden aufgrund der Abbindeeigenschaften drei bis vor kurzem nicht spektroskopisch unterscheidbare Sub-Phasen postuliert: Anhydrit II schwerlöslich (300-500°C, AII-s), unlöslich (500-700°C, AII-u) und Estrichgips (> 700°C, AII-E). Anhydrit I ist nur über 1180°C stabil. Mittels strukturanalytischer Methoden wie Röntgenbeugung (XRD) und Raman-Spektroskopie lassen sich nur die verschiedenen Hydratstufen sowie AIII, AII und AI eindeutig aufgrund unterschiedlicher Kristallstrukturen identifizieren. Ein neues auf Raman-mikrospektroskopischer Bildgebung basierendes Verfahren ermöglicht den Nachweis verschiedener Brenntemperaturen aufgrund der Auswertung von Raman-Bandenbreiten von AII, welche ein Maß für die mit steigender Brenntemperatur zunehmende Kristallinität der Anhydritkörner sind. Die Anwendung dieser Methode sowie der Nachweis pyrometamorpher Umwandlun-gen von Begleitmineralien aus dem Gipsstein als Mineralthermometer zur Bestimmung von Brenntemperaturen wird anhand von Proben früh- und spätmittelalterlicher Skulpturen und Stuckdekorationen aus Südtirol diskutiert. Außerdem wird gezeigt, wie die Analyse solch komplexer Materialien Rückkopplungen in die Analytische Chemie erzeugen kann, da zur erfolgreichen Analytik eine Möglichkeit zur reproduzierbaren Bestimmung von Ramanbandenbreiten und der Korrektur instrumentenabhängiger Verbreiterung gefunden und optimiert werden musste. Damit sollten überzeugende Belege dafür erbracht werden können, dass die Komplexität des monomineralischen Bindemittels Gips bezüglich der je nach Brandbedingungen unterschiedlichen Eigenschaften und insbesondere bezüglich der Herausforderungen an die Analytische Chemie häufig unterschätzt wird. T2 - ANAKON 2019 CY - Münster, Germany DA - 25.03.2019 KW - Gips KW - Anhydrit KW - Ramanspektroskopie PY - 2019 AN - OPUS4-48101 LA - deu AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - JOUR A1 - Abad Andrade, Carlos Enrique A1 - Florek, S. A1 - Becker-Ross, H. A1 - Huang, M.-D. A1 - de Oliveira Guilherme Buzanich, Ana A1 - Radtke, Martin A1 - Lippitz, Andreas A1 - Hodoroaba, Vasile-Dan A1 - Schmid, Thomas A1 - Heinrich, Hans-Joachim A1 - Recknagel, Sebastian A1 - Jakubowski, Norbert A1 - Panne, Ulrich T1 - Zirconium permanent modifiers for graphite furnaces used in absorption spectrometry: understanding their structure and mechanism of action N2 - The mechanism of action of zirconium permanent modifiers on graphite surfaces was investigated in order to understand its influence on the analytical signal in atomic and molecular absorption spectrometry (AAS/MAS). For this, the molecule formation of CaF was studied, which is used for the indirect analytical determination of fluorine in high-resolution continuum source graphite furnace molecular absorption spectrometry (HR-CS-GFMAS). The kinetics of this reaction was established by monitoring its molecular spectrum at different atomisation temperatures. An Arrhenius plot showed a pseudo-first order reaction with respect to fluorine (n = 1). An intermediate state was isolated, and its structure was elucidated by spectroscopic methods: scanning electron microscopy with energy dispersive X-ray spectroscopy (SEMEDX), X-ray photoelectron spectroscopy (XPS), X-ray absorption spectroscopy (XANES and EXAFS), and Raman microspectroscopy. We propose here a mechanism, where ZrO2 acts as a heterogeneous catalyst: after a pyrolytic step, an intermediate state of ZrO(OCaF) is activated, and at higher temperatures, CaF(g) is released from the zirconium-coated graphite surface. No evidence of the formation of zirconium carbide was found. Consequently, as the CaF formation is catalysed by a heterogeneous catalyst, surface modifications with ZrO2 nanoparticles and ZrO xerogels were investigated in order to increase the surface area. Their influence was evaluated in the molecule formation of CaF, CaCl, CaBr, and CaI. Graphite furnace modification with zirconium oxide nanoparticles proves to be the best choice for fluorine analysis with a signal enhancement of more than eleven times with respect a non-coated graphite furnace. However, the influence of zirconium modifications in the analytical signals of Cl, and I is lower than the F signals or even negative in case of the Br. Understanding zirconium modifiers as heterogeneous catalysts offers a new perspective to AAS and MAS, and reveals the potential of surface analytical methods for development of improved permanent modifiers and graphite furnace coatings. KW - Zirconium KW - HR-CS-MAS KW - Graphite furnace KW - Nanoparticles KW - Xerogel KW - Calcium monofluoride KW - Absorption spectrometry PY - 2018 UR - https://pubs.rsc.org/en/content/articlelanding/2018/ja/c8ja00190a DO - https://doi.org/10.1039/C8JA00190A SN - 0267-9477 VL - 33 IS - 12 SP - 2034 EP - 2042 PB - Royal Society of Chemistry AN - OPUS4-46775 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -