TY - CONF A1 - Stephan-Scherb, Christiane T1 - Unravelling high temperature oxidation phenomena by in situ x-ray techniques N2 - Unravelling high temperature oxidation phenomena by in situ x-ray techniques. A multi techqnique approach to study high temperature gas corrosion is presented. T2 - Gordon Research Conference on High Temperature Corrosion CY - New London, NH, USA DA - 20.07.2019 KW - Corrosion KW - High temperature KW - Diffraction KW - Spectroscopy PY - 2019 AN - OPUS4-48772 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Wander, Lukas A1 - Vianello, A. A1 - Vollertsen, J. A1 - Braun, Ulrike A1 - Paul, Andrea T1 - Multivariate analysis of large µ-FTIR datasets in search of microplastics N2 - µ-FTIR spectroscopy is a widely used technique in microplastics research. It allows to simultaneously characterize the material of the small particles, fibers or fragments, and to specify their size distribution and shape. Modern detectors offer the possibility to perform two-dimensional imaging of the sample providing detailed information. However, datasets are often too large for manual evaluation calling for automated microplastic identification. Library search based on the comparison with known reference spectra has been proposed to solve this problem. To supplement this ‘targeted analysis’, an exploratory approach was tested. Principal component analysis (PCA) was used to drastically reduce the size of the data set while maintaining the significant information. Groups of similar spectra in the prepared data set were identified with cluster analysis. Members of different clusters could be assigned to different polymer types whereas the variation observed within a cluster gives a hint on the chemical variability of microplastics of the same type. Spectra labeled according to the respective cluster can be used for supervised learning. The obtained classification was tested on an independent data set and results were compared to the spectral library search approach. T2 - CEST 2019 CY - Rhodes, Greece DA - 04.09.2019 KW - FTIR KW - Microplastics KW - Multivariate data analysis PY - 2019 AN - OPUS4-48889 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Geißler, Daniel A1 - Resch-Genger, Ute T1 - Development of reference materials (WP1) and reference methods (WP2) for the standardisation of concentration measurements of extracellular vesicles N2 - BAM provides leading expertise in preparation, characterisation and application of fluorescent reference standards and biomedical relevant nanomaterials, as well as in traceable, absolute, and quantitative fluorometric measurements of transparent and scattering systems in the ultraviolet, visible, and near infrared spectral region. BAM will prepare solid low-RI particles in WP1, will develop reference methods to determine the fluorescence intensity and RI of reference materials in WP2, and will measure the fluorescence intensity of EVs in biological test samples of WP3. T2 - EMPIR 18HLT01 "MetVesII" Kick-off meeting CY - Delft, The Netherlands DA - 17.06.2019 KW - Reference materials KW - Reference methods KW - Extracellualr vesicles PY - 2019 AN - OPUS4-48813 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Mirtsch, Mona A1 - Blind, K. T1 - Exploring the Diffusion of the ISMS Standard ISO/IEC 27001 N2 - We presented and discussed the applicability of Web Mining to explore the Diffusion of Management System Standards, in particular in regards to Information Security T2 - EURAS Conference CY - Rome, Italy DA - 14.06.2019 KW - Diffusion KW - Management system standard KW - Information security KW - Web Mining PY - 2019 AN - OPUS4-49029 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Resch-Genger, Ute A1 - Kage, Daniel A1 - Weigert, Florian A1 - Martynenko, Irina A1 - Dhamo, Lorena A1 - Soares, J. X. T1 - Luminescent nanocrystals – Photophysics and applications for lifetime multiplexing N2 - Bioanalytical, diagnostic, and security applications require the fast and sensitive determination of a steadily increasing number of analytes or events in parallel in a broad variety of detection formats.[1,2] Ideal candidates for spectral encoding and multiplexing schemes are luminescent nanocrystals like semiconductor quantum dots (QDs), particularly Cd-containing II/VI QDs with their narrow and symmetric emission bands. With the availability of relatively simple and inexpensive instrumentation for time-resolved fluorescence measurements, similar strategies utilizing the compound-specific parameter fluorescence lifetime or fluorescence decay kinetics become increasingly attractive.[3-5] The potential of different types of QDs like II/VI, III/V and Cd-free ternary QDs such as AgInS (AIS) QDs for lifetime-based encoding and multiplexing has been, however, barely utilized, although the lifetimes of these nanocrystals cover a time windows which is barely accessible with other fluorophores. Here we present a brief insight into the photophysics of AIS QDs and show the potential of dye- and QD-encoded beads for lifetime-based encoding and detection schemes in conjunction with flow cytometry and fluorescence lifetime imaging microscopy T2 - Nanax 2019 CY - Hamburg, Germany DA - 16.09.2019 KW - Nano KW - Microparticle KW - Bead KW - Encoding KW - Lifetime KW - Multiplexing KW - Flow cytometry KW - Bead-based assay KW - Fluorescence KW - Dye KW - LT-FCM KW - Time-resolved flow cytometry KW - Method PY - 2019 AN - OPUS4-49039 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Maiwald, Michael A1 - Foley, D. A. T1 - Analysis of dynamic systems N2 - Monitoring specific information (i.e., physico-chemical properties, chemical reactions, etc.) is the key to chemical process control when looking at dynamic systems, and quantitative online NMR spectroscopy is the method of choice for the investigation and understanding of dynamic multi-component systems. NMR provides rapid and non-invasive information, and due to the inherent linearity between sample concentration and signal intensity, peak areas can be directly used for quantification of multiple components in a mixture (without the need for any further calibration). This is one of the most attractive features of quantitative NMR spectroscopy. With the launch of devices covering magnetic field strengths from 40 to 90 MHz, so called compact or benchtop NMR systems, this analytical method is now reaching a sufficient degree of compactness and operability for an application outside of very specialized laboratories. Whilst there are also many other tools available to examine various analytical parameters from dynamic processes, such as mass spectrometry, (near) infrared or Raman spectroscopy, each of these tools can only really be used independently. How can we examine and compare all data describing a particular chemical reaction? How can we visualize information rich, specific, or direct methods together with less specific but established analytical methods? And how can we transfer calibration information to the most appropriate process analytical method or method combination? Quantitative NMR spectroscopy (qNMR) has the potential to substitute offline laboratory analysis for calibration purposes by delivering quantitative reference data as an online method. The workshop briefly presents the current state of the art of the analysis of dynamic systems by online NMR spectroscopy and analytical data fusion, with the remaining time being used for questions and open discussion with the attendees. T2 - SMASH 2019 CY - Porto, Portugal DA - 22.09.2019 KW - Process Analytical Technology KW - Reaction Monitoring KW - Online NMR Spectroscopy KW - Data Analysis KW - SMASH PY - 2019 UR - https://www.smashnmr.org/ AN - OPUS4-49042 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Denkler, Tilman T1 - Introduction meeting FINAS - Analysis of the operation of accreditation bodies in Europe N2 - The long-term goal of the benchmarking project for European accreditation bodies is twofold: First of all, the project is supposed to help the European accreditation attending bodies to improve their processes by identifying best practices and by learning from others. Possibly Secondly, the results of the analysis can be used by the European Cooperation for Accreditation (EA) to identify differences in the operation of the European accreditation bodies and based on this knowledge to promote harmonization of accreditation activities in Europe. T2 - Kick-off at FINAS, Helsinki CY - Helsinki, Finland DA - 19.08.2019 KW - Accreditation KW - Benchmarking PY - 2019 AN - OPUS4-49046 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Denkler, Tilman T1 - Introduction meeting accredia - Analysis of the operation of accreditation bodies in Europe N2 - The long-term goal of the benchmarking project for European accreditation bodies is twofold: First of all, the project is supposed to help the European accreditation attending bodies to improve their processes by identifying best practices and by learning from others. Possibly Secondly, the results of the analysis can be used by the European Cooperation for Accreditation (EA) to identify differences in the operation of the European accreditation bodies and based on this knowledge to promote harmonization of accreditation activities in Europe. T2 - Kick-off at Accredia, Milano CY - Mailand, Italy DA - 28.08.2019 KW - Accreditation KW - Benchmarking PY - 2019 AN - OPUS4-49047 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Radnik, Jörg A1 - Kunz, Valentin A1 - Schneider, Markus A1 - Nymark, Penny A1 - Grafström, Roland A1 - Unger, Wolfgang T1 - Combining surface analytic and toxicity data for safer nanomaterials N2 - Nanomaterials are present in our everyday life. Paint coats, sunscreens, catalysts and additives for tyres are good examples for the use of such materials in mass-market products. The problem of the safety of nanomaterials is recognized as a problem for health and environment, which lead to the special registration of nanomaterials according to an annex of REACH as of 2020. But a great problem for the risk assessment of nanomaterials that several factors could influence the hazardous nature of them. Additional to composition, crystal structure, size and shape the surface properties of such particles belong to these parameters for risk assesment. The reason for the relevance of the surface is obvious: the smaller the particle, the higher is the share of the surface. Additionally, the surface is the region of the particle which interacts with the surrounding which is another crucial factor for the understanding the effect of a nanomaterial on health and environment. In the OECD Testing Programme on Manufactured Nanomaterials exists consequently an Endpoint 4.30 Surface Chemistry in Chapter 4. PHYSICAL AND CHEMICAL PROPERTIES. In summary, there is obviously a need for a correlation between surface chemical analytic data and toxicity. To fill in this gap, we present surface analytic results obtained with X-ray photoelectron spectroscopy and Time-of-Flight Secondary Ion Mass Spectrometry and correlate them with cytotoxic data gain by high-throughput screening experiments. It must be noted, that these experiments were done at the same set of titania materials taken from the JRC (Joint Research Centre of the European Union) Nanomaterials Repository. As material TiO2 was chosen due to its widespread use in consumer products, e.g. paint coats and sunscreens. With this new approach a better understanding of the influence of surface properties on the toxicity can be expected leading to a better risk assessment of these materials. T2 - ECASIA 2019 CY - Dresden, Germany DA - 15.09.2019 KW - Risk assessment KW - Nanomaterials KW - Surface analytic KW - Toxicology PY - 2019 AN - OPUS4-49090 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Crasselt, Claudia A1 - Schmidt, Wolfram A1 - Sturm, Heinz T1 - Influence of rheology modifying admixtures on early hydration of cementitious suspensions N2 - The presence of polycarboxylate ether (PCE) based superplasticizers (SPs) has enormous influence on the early hydration of cement. C3A as the most reactive phase of Portland cement plays a significant role in early hydration reactions and affects the rheological performance. Therefore, this talk presents experimental results about the influence of delayed addition of PCEs on the Hydration of alite and C3A-gypsum pastes investigated by isothermal heat flow calorimetry. Complementary in-situ XRD was carried out on C3S and C3A-gypsum pastes to analyze hydration and phase changes related to the addition of PCE. Cement pastes with a delayed addition of PCE showed less retardation compared to simultaneous addition. The alteration caused by PCE is much more pronounced for C3A-gypsum mixes. With a delayed addition of SP, the hydration of C3A is less retarded or even accelerated. It is obvious that there is less retardation the later the addition of SP. Furthermore, the PCE alter the hydration of C3A when added delayed and exhibit changes in kinetics and Hydration rates. XRD results showed that more C3A is dissolved in the presence of PCE. Also, the gypsum depletion occurs earlier in the presence of PCE and even faster with delayed addition. Without PCE AFm starts to form just after the gypsum depletion. However, in the presence of PCE AFm already starts to form at the beginning of the hydration. Due to the faster gypsum depletion in the presence of PCE, also the transformation from ettringite into AFm begins earlier, but takes longer as without SP. T2 - 15th International Congress on the Chemistry of Cement CY - Prague, Czech Republic DA - 16.09.2019 KW - Cement KW - Alite KW - C3S KW - C3A KW - Early hydration KW - Polycarboxylate ether (PCE) KW - Delayed addition PY - 2019 AN - OPUS4-49103 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Vogel, Christian A1 - Huang, L. A1 - Sekine, R. A1 - Doolette, A. A1 - Herzel, Hannes A1 - Kugler, Stefan A1 - Hoffmann, Marie A1 - Lombi, E. A1 - Zuin, L. A1 - Wang, D. A1 - Félix, R. A1 - Adam, Christian T1 - Specification of bioavailable nutrients and pollutants in the environment by combining DGT and spectroscopic techniques N2 - Previous research shows that analytical methods based on Diffusive Gradients in Thin films (DGT) provide very good correlations to the amount of bioavailable nutrients and pollutants in the environmental samples. However, these DGT results do not identify which compound of the specific element has the high bioavailability. Using various spectroscopic techniques (infrared, XANES and NMR spectroscopy) to analyze the dried DGT binding layers after deployment could allow us to determine the specific elements or compounds. Nutrients such as phosphorus and nitrogen are often, together with other elements, present as molecules in the environment. These ions are detectable and distinguishable by infrared and NMR spectroscopy, respectively. In addition, XANES spectroscopy allows for the specification of nutrients and pollutants (e.g. chromium) on the DGT binding layer. Furthermore, microspectroscopic techniques make it also possible to analyze compounds on the DGT binding layer with a lateral resolution down to 5 µm2. Therefore, species of elements and compounds of e.g. a spatial soil segment can be mapped and analyzed, providing valuable insight to understand the dynamics of nutrients and pollutants in the environment. Here we will present the advantages and limitations of this novel combination of techniques. T2 - 6th Conference on Diffusive Gradients in Thin Films CY - Vienna, Austria DA - 17.09.2019 KW - Soil P species KW - DGT KW - Infrared spectroscopy PY - 2019 AN - OPUS4-49057 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Braun, Ulrike T1 - Harmonization in microplastics Analysis N2 - The lecture summarizes the current status of hamonization edr microplastics analytics in Germany. T2 - Symposium on Occurrence and Fate of Microplastics CY - Beijing, China DA - 09.07.2019 KW - Microplastics KW - TED-GC-MS KW - Harmonisation PY - 2019 AN - OPUS4-49063 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Dudek, Gabriele A1 - Koch, Claudia T1 - Accreditation, conformity assessment and national Quality Infrastructure - The system in Germany and areas of research N2 - The presntation gives an overview of the QI System in Germany and Europe, especially accreditation and conformity assessment. It further highlights some areas of research conducted in BAM with regard to elements of QI. T2 - National Quality Infrastructure • Beijing Forum CY - Peking, People's Republic of China DA - 08.01.2019 KW - QI KW - Accreditation KW - Quality infrastructure KW - Qualitätsinfrastruktur KW - Conformity assessment KW - Konformitätsbewertung KW - Akkreditierung PY - 2019 AN - OPUS4-49123 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Koch, Claudia A1 - Dudek, Gabriele T1 - Accreditation, conformity assessment and national quality infrastructure - The system in Germany and areas of research N2 - The presentation gives an overview and some examples of research projects conducted at BAM (Department S.2) in the field of QI T2 - National Quality Infrastructure • Beijing Forum CY - Peking, People's Republic of China DA - 08.01.2019 KW - QI KW - Qualitätsinfrastruktur KW - Quality infrastructure KW - Conformity assessment KW - Konformitätsbewertung KW - Standardization KW - Normung KW - Akkreditierung KW - Accreditation PY - 2019 AN - OPUS4-49124 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bernegger, Raphael A1 - Altenburg, Simon A1 - Maierhofer, Christiane T1 - Pulsed thermography on semitransparent materials - what has to be considered? N2 - Pulsed thermography is a well-known non-destructive testing technique and has proven to be a valuable tool for examination of material defects, to determine thermal material parameters, and the thickness of test specimens through calibration or mathematical models. However, the application to semitransparent materials is quite new and demanding, especially for semitransparent materials like epoxy, polyamide 12, or glass fiber reinforced polymers with epoxy or polyamide matrix. In order to describe the temporal temperature evolution in such materials, which are recorded with an infrared camera during pulse thermography experiments, much more influences have to be considered, compared to opaque materials: - The wavelength of the excitation source and the spectral range of the infrared camera - The angles between the specimen, the excitation source and the infrared camera - The area behind the specimen - The roughness of the material surface - The scattering mechanism within the material Here, we will consider all these influences and describe how they can be treated mathematically in analytical or numerical models (using COMSOL Multiphysics software). These models describe the temperature development during the pulse thermography experiment in reflection and transmission configuration. By fitting the results of the mathematical models to experimental data it is possible to determine the thickness or the optical and thermal properties of the specimen. T2 - 20-th International Conference on Photoacoustic and Photothermal Phenomena CY - Moscow, Russia DA - 07.07.2019 KW - Numerical simulation KW - Pulsed thermography KW - Semitransparent KW - Analytical model KW - Delamination KW - GFRP PY - 2019 AN - OPUS4-49215 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Nehring, Grzegorz A1 - Pronobis-Gajdzis, M. A1 - Targowski, P. A1 - Rabin, Ira T1 - What should we take into an account in the characterization of iron-gall ink by means of X-ray fluorescence? N2 - The earliest known recipes for iron gall inks include four basic ingredients: oak galls – pathological growths of oak leaves; metal salts – usually referred to as vitriol; a binder such as gum Arabic; and water. The final product differs in the elemental composition due to the multitude of recipes as well as differences within the composition of the ink’s ingredients. Nowadays, based on the qualitative and semi-quantitative evaluation of X-ray fluorescence data, it is possible to distinguish inks on the basis of the so-called fingerprint model. The first goal of our study was to determine to what extent the type of XRF spectrometer affects the quality of the ink evaluation. We tested two types of spectrometers, semi-stationary machines equipped with polycapillary focusing optics and a handheld spectrometer with a diaphragm collimator and a relatively big interaction spot. The second goal was to address the issue of whether the ink composition might be affected by storage in a metal container. The presentation will discuss the role of the spectrometer type in the evaluation of a thin layer material such as ink. We have also learned that the iron-gall ink composition might depend on the type of vessel in which ink was being stored. T2 - Konferenz - XIV IADA Congress - Warsaw 2019 CY - Warsaw, Poland DA - 23.09.2019 KW - Iron-gall ink KW - XRF KW - Inkwells KW - Ink composition PY - 2019 AN - OPUS4-49149 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Gojani, Ardian A1 - Palásti, David J. A1 - Paul, Andrea A1 - Galbacs, G. A1 - Gornushkin, Igor B. T1 - Application of spatial heterodyne spectroscopy for chemical analysis based on Raman and laser-induced breakdown spectroscopy N2 - Spatial Heterodyne Spectroscopy (SHS) is a spectrometric technique that combines both dispersive and interferometric features into a customizable instrument. The Basis of SHS is a Michelson interferometer with its mirrors replaced by diffraction gratings and with no moving parts. The output signal from SHS is the interferogram, which is recorded with a 1D or 2D pixel array detector. The spatial periodicity of the fringes on the interferogram is a function of the wavelength of the diffracted light. Using the Fast Fourier Transform, the original optical spectrum that enters SHS is retrieved. The light that is analyzed by SHS can come from a variety of sources. In our work, we used Raman scattering and Laser-Induced Plasma to perform quantitative and qualitative analyses. Figure 1 compares the performance of the SHS with that of high Resolution echelle and portable low-resolution asymmetrically crossed Czerny-Turner spectrometers (OO in Fig.1). The analyzed light came from the plasma induced on a stainless-steel reference material. The SHS exhibits the resolution comparable to that of the echelle spectrometer used, about 8000. Due to a high throughput of the SHS (theoretically, ~200 times higher than that of grating instruments), the number of spectra needed to be accumulated for comparable signal-to-noise ratios is much smaller than in the case of the echelle and comparable to OO spectrometers. Examples of Raman SHS applied to several pure liquids are given in Fig. 2. Raman SHS was used in three different settings: (i) for classification of six types of oils, (ii) for univariate/multivariate analysis of binary mixture cyclohexane-isopropanol, and (iii) for multivariate analysis of glycerol solution in water. For the last two settings, chemometric analysis of the spectra yielded linear calibration plots over the range 1-90% of concentrations of isopropanol in cyclohexane, and 0.5-10% of glycerol in water. T2 - ANAKON 2019 CY - Münster, Germany DA - 25.03.2019 KW - Spatial heterodyne spectroscopy KW - Raman spectroscopy KW - Laser-Induced Background Spectroscopy PY - 2019 AN - OPUS4-49176 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Müller, Anja A1 - Heinrich, Thomas A1 - Tougaard, S. A1 - Werner, W. S. M. A1 - Hronek, M. A1 - Kunz, Valentin A1 - Benemann, Sigrid A1 - Hodoroaba, Vasile-Dan A1 - Radnik, Jörg A1 - Stockmann, Jörg M. A1 - Nirmalananthan-Budau, Nithiya A1 - Geißler, Daniel A1 - Sparnacci, K. A1 - Unger, Wolfgang T1 - Determining thickness and completeness of the shell for polymer core shell nanoparticles by XPS, ToF SIMS and T SEM N2 - Core-shell nanoparticles (CSNPs) have become indispensable in various industrial applications. However, their real internal structure usually deviates from an ideal core-shell structure. To control how the particles perform with regard to their specific applications, characterization techniques are required that can distinguish an ideal from a non-ideal morphology. In this work, we investigated PTFE-PMMA (four samples) and PTFE-PS (six samples) polymer CSNPs with constant core diameter (45 nm) but varying shell thickness (4-50 nm). As confirmed by transmission scanning electron microscopy (T-SEM), the shell completely covers the core for the PTFE-PMMA nanoparticles, while the encapsulation of the core by the shell material is incomplete for the PTFE-PS nanoparticles. X-ray photoelectron spectroscopy (XPS) was applied to determine the shell thickness of the nanoparticles. The software SESSA V2.0 was used to analyze the intensities of the elastic peaks and the QUASES software package to evaluate the shape of the inelastic background in the XPS Survey spectra. For the first time, nanoparticle shell thicknesses are presented which are exclusively based on the analysis of the XPS inelastic background. Furthermore, principal component analysis (PCA) assisted time-of-flight secondary ion mass spectrometry (ToF-SIMS) of the PTFE-PS nanoparticle sample set revealed a systematic variation among the samples and, thus, confirmed the incomplete encapsulation of the core by the shell material. Opposed to that, no variation is observed in the PCA scores plots of the PTFE-PMMA nanoparticle sample set. Consequently, the complete coverage of the core by the shell material is proved by ToF-SIMS with a certainty that cannot be achieved by XPS and T-SEM. T2 - 18th European Conference on Applications of Surface and Interface Analysis (ECASIA) CY - Dresden, Germany DA - 15.09.2019 KW - Core-shell nanoparticles KW - Polymers KW - ToF-SIMS KW - XPS KW - XPS background analysis PY - 2019 AN - OPUS4-49187 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Langklotz, U. A1 - Babutzka, Martin A1 - Burkert, Andreas A1 - Schneider, M. T1 - FT-IR spectroscopy of corrosion products formed on zinc under atmospheric conditions N2 - Zinc materials are of high importance in the field of corrosion protection. For example, almost half of the annual production of zinc is used as anti-corrosive layer for steel components, particularly under atmospheric conditions. The corrosion protection is frequently ascribed to zinc carbonate species with low solubility which form on the metal surface under atmospheric conditions. Due to the technological importance and wide use of zinc materials, its corrosion behavior and the formation of reaction products has been intensively investigated over decades. Assuming atmospheric corrosion conditions, an initial native passive film of few nanometers thickness forms spontaneously. It consists of zinc oxide and hydroxide, transforming into various species in dependence of the surrounding atmospheric conditions. This study focusses on the investigation of corrosion product layers on massive titanium-zinc sheets, formed during short- and mid-term exposure experiments by Fourier-transformed infrared spectroscopy. This method enables the investigation of extremely thin native passive films which form during the initial hours of exposure. Furthermore, aged surface layers are analyzed which were formed by transformation of initial passive layers over the time of several weeks. The spectroscopic investigations are complemented by scanning electron microscopy (SEM/EDX) in order to obtain information on the chemical composition and morphology of the corrosion products. The combination of both methods offers a comprehensive view on the processes occurring in the early stages of zinc corrosion. T2 - EUROCORR 2019 CY - Sevilla, Spain DA - 09.09.2019 KW - Zinc coatings KW - FT-IR KW - Layer formation PY - 2019 AN - OPUS4-49132 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Nehring, Grzegorz A1 - Targowski, P. A1 - Rabin, Ira T1 - Can an inkwell leak into ink? N2 - X-ray fluorescence analysis, due to its non-destructive nature and ist suitability to work with historic objects in situ, quickly became one of the most important methods for the evaluation of iron-gall ink. The main advantage of this qualitative and semi-quantitative method is that it makes it easy to differentiate between inks, based on the assumption that the differences result from the manufacture of the ink. This work explores the question whether the ink ‘fingerprint’ results strictly from the elemental composition of the basic ink ingredients even if it is stored in vessels made of metals or metal alloys. In addition, we tested and compared the performance of three different XRF spectrometers. We prepared various lab-grade inks according to historical ink recipes and measured the metal content of the ink deposited on sized cotton Linters paper with three types of XRF spectrometers: a simple hand-held device with an interaction spot of 4 mm and two devices equipped with poly-capillary Xray optics for line scanning and imaging. Since the exact elemental mass composition of the non-aged ink samples was known, we were able to evaluate the accuracy of the research procedure. Lab-grade inks were then aged in the metal jars imitating inkwells. The aging of the inks in the metal containers resulted in the significant change of the primary inks fingerprint as opposed to that of the control inks stored in glass containers. This effect was independently confirmed by the measurements conducted with every instrument we used. We will present a brief comparison of the results 43 achieved when using different spectrometers and a possible hypothesis explaining the processes that occurred. T2 - Konferenz -7th Meeting X-ray and other techniques in investigations of the objects of cultural heritage CY - Krakow, Poland DA - 17.05.2018 KW - Iron-gall ink KW - XRF KW - Inkwells KW - Ink composition KW - Performance comparison PY - 2018 AN - OPUS4-49157 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -