TY - CONF A1 - Kern, Simon A1 - Michalik-Onichimowska, Aleksandra A1 - Riedel, Jens A1 - Panne, Ulrich A1 - King, R. A1 - Maiwald, Michael T1 - “Click” analytics for “click” chemistry – a simple method for calibration-free evaluation of online NMR spectra N2 - Currently research in chemical manufacturing moves towards flexible plug-and-play approaches focusing on modular plants, capable of producing small scales on-demand with short down-times between individual campaigns. This approach allows for efficient use of hardware, a faster optimization of the process conditions, and thus, an accelerated introduction of new products to the market [1]. Driven mostly by the search for chemical syntheses under biocompatible conditions, so-called “click” chemistry rapidly became a growing field of research. The resulting simple one-pot reactions are so far only scarcely accompanied by an adequate optimization via comparably straightforward and robust analysis techniques. Here we report on a fast and reliable calibration-free online high field NMR monitoring approach for technical mixtures. It combines a versatile fluidic system, continuous-flow measurement with a time interval of 20 s per spectrum, and a robust, automated algo-rithm to interpret the obtained data. All spectra were acquired using a 500 MHz NMR spectrometer (Varian) with a dual band flow probe having a 1/16 inch polymer tubing working as a flow cell. Single scan 1H spectra were recorded with an acquisition time of 5 s, relaxation delay of 15 s. T2 - 11. Doktorandenseminar 2017 des Arbeitskreis Prozessanalytik der GDCh und DECHEMA CY - Berlin, Germany DA - 12.03.2017 KW - Online NMR Spectroscopy KW - Click chemistry KW - Data analysis PY - 2017 AN - OPUS4-39397 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kern, Simon A1 - Michalik-Onichimowska, Aleksandra A1 - Riedel, Jens A1 - Panne, Ulrich A1 - King, R. A1 - Maiwald, Michael T1 - “Click” analytics for “click” chemistry – a simple method for calibration-free evaluation of online NMR spectra N2 - Currently research in chemical manufacturing moves towards flexible plug-and-play approaches focusing on modular plants, capable of producing small scales on-demand with short down-times between individual campaigns. This approach allows for efficient use of hardware, a faster optimization of the process conditions, and thus, an accelerated introduction of new products to the market. Driven mostly by the search for chemical syntheses under biocompatible conditions, so-called “click” chemistry rapidly became a growing field of research. The resulting simple one-pot reactions are so far only scarcely accompanied by an adequate optimization via comparably straightforward and robust analysis techniques. Here we report on a fast and reliable calibration-free online high field NMR monitoring approach for technical mixtures. It combines a versatile fluidic system, continuous-flow measurement with a time interval of 20 s per spectrum, and a robust, automated algorithm to interpret the obtained data. All spectra were acquired using a 500 MHz NMR spectrometer (Varian) with a dual band flow probe having a 1/16 inch polymer tubing working as a flow cell. Single scan 1H spectra were recorded with an acquisition time of 5 s, relaxation delay of 15 s. As a proof-of-concept, the thiol-ene coupling between N-boc cysteine methyl ester and allyl alcohol was conducted in non-deuterated solvents while its time-resolved behaviour was characterised with step tracer experiments Through the application of spectral modeling the signal area for each reactant can be deconvoluted in the online spectra and thus converted to the respective concentrations or molar ratios. The signals which were suitable for direct integration were used herein for comparison purposes of both methods. T2 - EuroPACT 2017 CY - Potsdam, Germany DA - 10.05.2017 KW - Online NMR Spectroscopy PY - 2017 AN - OPUS4-40283 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bruno, Giovanni A1 - Kupsch, Andreas A1 - Mueller, Bernd R. A1 - Lange, Axel T1 - X-ray refraction 2D and 3D techniques N2 - X-ray refraction techniques represent a very promising, yet not so wide-spread, set of X-ray techniques based on refraction effects. They allow determining internal specific surface (surface per unit volume) in a non-destructive fashion, position and orientation sensitive, and with nanometric detectability. While they are limited by the X-ray absorption of the material under investigation, we demonstrate showcases of ceramics and composite materials, where understanding of microstructural features could be achieved in a way unrivalled even by high-resolution techniques such as electron microscopy or computed tomography. T2 - ICTMS 2017 CY - Lund, Sweden DA - 26.06.2017 KW - X-ray refraction KW - Composites KW - Damage KW - Cracks KW - Cearmics PY - 2017 AN - OPUS4-41042 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Usmani, Shirin A1 - Schlishka, Joerg A1 - Klutzny, Kerstin A1 - de Laval, Yvonne A1 - Plarre, Rüdiger A1 - Krahl, Thoralf A1 - Stephan, Ina A1 - Huebert, Thomas A1 - Kemnitz, Erhard T1 - Wood protection with nanoparticles: MgF2 and CaF2 N2 - Alkaline earth metal fluoride nanoparticles have been investigated for application in wood protection. Sols of MgF2 and CaF2 were synthesized and their efficacy was tested against fungi and termites (Rehmer 2016, Krahl et al. 2016). The sols were characterized by XRD and SEM. The wood specimens were vacuum impregnated with nanoparticles and then exposed to fungi and termites according to EU certified test conditions. Our results show that wood impregnated with metal fluoride nanoparticles significantly reduce cellulose hydrolysis by fungi and termites. The wood samples were exposed to brown-rot fungi; Coniophora puteana and Poria placenta. Between the two fungi, the overall mass lost due to fungal degradation was lower for treated (MgF2 and CaF2) wood samples exposed to Coniophora puteana. Thus, the metal fluoride nanoparticles impregnated in the wood samples were more efficient in reducing cellulose degradation from Coniophora puteana than from Poria placenta. However the mass loss in samples treated with MgF2 was similar to those treated with CaF2, irrespective of type of fungi. Therefore, it is likely that fungal degradation in treated samples was dependent on the biocidal action of fluorides rather than on the differences in chemical and physical properties of MgF2 and CaF2, respectively. Conversely, for termite exposure, wood samples treated with MgF2 had lower cellulose degradation compared to those treated with CaF2. A possible explanation for this difference in results could be fungi and termites use separate mechanisms for cellulose hydrolysis which will be further investigated. Future experiments include testing the leaching potential of MgF2 and CaF2 nanoparticles from wood. The results from the leaching experiment will test if metal fluoride nanoparticles can provide long-term and environmentally safe protection to wood. T2 - International Research Group (IRG48) Scientific Conference on Wood Protection CY - Ghent, Belgium DA - 04.06.2017 KW - Fluoride KW - Nanoparticles KW - Brown-rot fungi KW - Termites PY - 2017 AN - OPUS4-41019 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hodoroaba, Vasile-Dan A1 - Wohlleben, W. A1 - Mielke, Johannes A1 - Rauscher, H. T1 - Volume specific surface area (VSSA) by BET: concept and demonstration on industrial materials N2 - Volume specific surface area (VSSA) as measured by BET constituites a simple and reliable solution to (most) powders. Porous, coated, polydisperse/multimodal materials are to be treated with care, i.e. doubled by analysis with electron microscopy or more advanced BET analysis (e.g. t-plot)for each material in part. T2 - Final NanoDefine Outreach Event: Classification of nanomaterials according to the EU definition CY - Brüssel, Belgium DA - 19.09.2017 KW - VSSA KW - BET KW - Nanoparticles KW - Powder KW - Nanomaterial classfication PY - 2017 UR - http://www.nanodefine.eu/index.php/nanodefine-meetings/125-final-outreach-event-2017 AN - OPUS4-42509 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Asadujjaman, Asad A1 - Ahmadi, Vahid T1 - Upper critical solution temperature (UCST)- type thermoresponsive polymers from acrylamide-based monomers N2 - UCST-type thermoresponsive polymers that phase separate from solution upon cooling present a tremendous potential not only in aqueous media where they can be used in drug delivery, diagnostic and microfluidic applications, but also in water/alcohol mixtures, where they can be used for instance in sensing systems for alcohol-soluble drugs. However, only a few thermoresponsive polymers have been reported that present an UCST in a relevant temperature range and “green” solvents such as water or ethanol. In this context, acrylamide-based monomers can be very useful building blocks for designing novel UCST-type polymers because of their hydrophilic nature (with the right side chain) and propensity to form hydrogen bonds. We want to present our latest results on the copolymer poly(acrylamide-co-acrylonitrile) (P(AAm-co-AN)) that present a UCST in water as well as on two homopolymers based on an acrylamide derivative of 2,6-diaminopyridine, namely poly(N-(6-aminopyridin-2-yl)acrylamide) (PNAPAAm) and poly(N-(6-acetamidopyridin-2-yl)acrylamide) (PNAcAPAAm) that show UCST-type thermoresponsiveness in water/alcohol mixtures. Our focus for P(AAm-co-AN)) is its aggregation behaviour above and below its phase transition temperature as the size of thermoresponsive polymeric systems is of prime importance for biomedical applications (as size dependent processes take place in the body) and is linked to the optical properties of a material that matter in materials science. In the case of PNAPAAm and PNAcAPAAm, we focused on the co-solvency/co-non solvency effect on the phase transition temperature in water/alcohol mixture. Indeed, polymers with UCST behavior below 60°C in water/alcohol mixtures are extremely promising for the preparation of “smart” materials for sensing. T2 - 31st Conference of the European Colloid and Interface Society (ECIS 2017) CY - Madrid, Spain DA - 03.09.2017 KW - Thermoresponsive polymers KW - UCST polymers KW - Acrylamide based polymers PY - 2017 AN - OPUS4-41902 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kästner, Claudia A1 - Thünemann, Andreas T1 - Tuning the catalytic activity of silver nanoparticles N2 - The use of silver nanoparticles in consumer related products has significantly increased over the last decade, especially due to their antimicrobial properties. Today they are used in a variety of products, which range from textiles to dietary supplements. Thus, investigations on nanoscale silver become increasingly important in many fields like biomedicine or catalysis. Unfortunately, the results of these studies are extremely diverse and do not lead to a consistent evaluation of the toxicity of silver nanoparticles. The main problem is the use of nonuniform and poorly characterized particles with broad size distributions. To overcome this problem we modified the known polyol process to synthesize ultra-small core-shell silver nanoparticles in a large scale. The particles are highly stable and show no aggregation for more than six months. Small-angle X-ray scattering analysis reveals a narrow size distribution of the silver cores with a mean radius of 3 nm and a distribution width of 0.6 nm. Dynamic light scattering provides a hydrodynamic radius of 10.0 nm and a PDI of 0.09. The stabilizing ligand PAA can be easily exchanged by biomolecules to modify the surface functionality. Replacements of PAA with glutathione and bovine serum albumin have been successfully performed. To demonstrate the broad applicability of our particles we performed catalysis experiments with the reduction of 4-nitrophenol as model reaction. The PAA-stabilized particles show a catalytic activity of (436 ± 24) L g-1 s-1, which is the highest reported in literature for silver nanoparticles. In contrast, GSH and BSA passivate the surface substantially resulting in lower catalytic activities. T2 - Australian Colloid and Interface Symposium 2017 CY - Coffs Harbour, New South Wales, Australia DA - 29.01.2017 KW - SAXS KW - Protein coating KW - Catalysis PY - 2017 AN - OPUS4-39203 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Abbas, Ioana M. A1 - Hoffmann, Holger A1 - Weller, Michael G. T1 - Troubleshooting for the clinical measurement of iron biomarkers using LC-MS/MS: Suppression of sample losses in autosampler vials N2 - We developed a rapid and robust HPLC-MS/MS (QqQ) method for the quantification of hepcidin-25, a promising new biomarker in iron metabolism, in human samples. The novelty of the method is the use of special HPLC vials to avoid adsorptive losses due to the basic character of the peptide that causes interaction with the silanol groups of the vial’s glass surface. Up to 90% decrease in the MS/MS signal was observed, when commercial HPLC vials were used, while vials treated with 3-(2-aminoethylamino)propylmethyldimethoxysilane or 1H,1H,2H,2H-perfluorooctyltriethoxysilane, leading to no losses in the range of physiological hepcidin-25 mean serum levels (10-20 µg/L). T2 - MSACL 2017 EU CY - Salzburg, Austria DA - 10.09.2017 KW - Peptide losses KW - Adsorption KW - Silanization PY - 2017 AN - OPUS4-44613 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Rades, Steffi A1 - Ortel, Erik A1 - Wirth, Thomas A1 - Holzweber, Markus A1 - Pellegrino, F. A1 - Martra, G. A1 - Hodoroaba, Vasile-Dan T1 - Tracing fluorine at the surface and in the bulk of TiO2 nanoplatelets by means of SEM-EDX, AES and ToF-SIMS N2 - The synthesis of TiO2 nanoplatelets with fluorine-containing reactants is carried out using titanium (IV) butoxide as precursor and concentrated HF as shape controller, the final product requires a working up in order to eliminate or at least to reduce the amount of residual fluorides, which is realized here by well-defined thermal treatment of the samples. Bulk and surface sensitive methods namely scanning electron microscopy with energydispersive X-ray spectroscopy (SEM-EDX), Auger electron spectroscopy (AES) and time-of-flight secondary ion mass spectrometry (ToF-SIMS) have been applied to trace the presence of any fluorides in dependence on different information depths and measurement sensitivities of these methods. T2 - EMAS 2017 - 15th European Workshop on MODERN DEVELOPMENTS AND APPLICATIONS IN MICROBEAM ANALYSIS and IUMAS-7 Meeting CY - Konstanz, Germany DA - 07.05.2017 KW - Nanoparticles KW - Surface analysis KW - ToF-SIMS KW - AES KW - SEM-EDX PY - 2017 AN - OPUS4-40265 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Koegler, M. A1 - Paul, Andrea A1 - Pellicer-Alborch, K. A1 - Anane, E. A1 - Birkholz, M. A1 - Bunker, A. A1 - Viitala, T. A1 - Junne, S. A1 - Neubauer, P. T1 - Time-gated Raman spectroscopy and SERS as advanced technologies in bioprocess monitoring N2 - Raman spectroscopy is becoming a powerful process analytical technology (PAT) tool. Until now Raman technology has not shown its full potential in bioprocess on-line monitoring due to several technical challenges. Because of only small? interference from water molecules, Raman-spectroscopy is in contrast to IR spectroscopy able to follow changes of metabolite concentrations in dilute aqueous solutions. Results from common CCD-based process Raman-spectrometers reveal only barely identifiable peaks with a dominating (fluorescence) background. To solve this, Raman spectroscopy needs: (A) an enhancement to increase the limit of detection (LOD), and (B) a reliable method to distinguish the Raman signal from the sample-related auto-fluorescence. SERS (surface enhanced Raman spectroscopy) acts as an optical "nano-antenna"-effect. It causes a dipolar localized surface Plasmon resonance effect due to noble metallic nanoparticles or roughened metal and improves the limit of detection (LOD) significantly. Another new process-monitoring technique, which removes the fluorescence background in Raman-measurements is called time-gated Raman spectroscopy. It uses a picosecond pulsed Nd:YVO4-laser as emission source (exc= 532 nm) and a gated SPAD-array (Single Photon Avalanche Detector) detector instead of commonly used CCD (Charged Coupled Device)-detectors and CW (Continues Wave) laser emission. Time-Gate can measure the Raman-signal before the stronger fluorescence signal reaches the detector. In this study we utilized both SERS (Surface Enhanced Raman Spectroscopy) and time-gated Raman spectroscopy (TG-Raman) in combination on cell-free supernatant samples of an Escherichia coli cultivation with mineral salt media and a lactic acid bacteria fermentation with complex media. As a reference method for the estimation of amino acids and other metabolites, HPLC-RID and HPLC-FLD were used to evaluate the Raman-based detection. The quantitative evaluation of Raman data was performed by multivariate data analysis such as principal component analysis (PCA) and partial least squares regression (PLSR). For the first time, we can show that both qualitative and quantitative measurements are conducted successfully with both, SERS and time-gated Raman methods in industrially relevant media, so that a fast and reliable in situ or bypassed concentration measurement becomes feasible. T2 - 2. Photonics Finland, Optics and Photonics Days 2017 CY - Oulu, Finland DA - 29.05.2017 KW - Time-gate Raman KW - PAT KW - Chemometrics PY - 2017 UR - http://www.photonics.fi/event/opd17-optics-photonics-days-2017/ AN - OPUS4-41182 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kage, Daniel A1 - Hoffmann, Katrin A1 - Witkamp, M. A1 - Ameskamp, J. A1 - Göhde, W. A1 - Thiele, T. A1 - Schedler, U. A1 - Resch-Genger, Ute T1 - Time domain flow cytometry utilizing lifetime-encoded polymer microparticles N2 - Flow cytometry is a widely used method in biological research and medical diagnostics. Depending on the respective application, two opposing directions of development are currently of interest. On the one hand, there is a need for analyses of growing complexity employing more and more fluorescent labels and codes. On the other hand, cost-effective methods and portable, miniaturized, and robust instruments are desired. Commonly performed spectral multiplexing utilizing a color code suffers from several problems, such as the sensitivity of fluorescence intensity measurements to fluctuations in excitation light intensity and dye concentration and hence, photobleaching, dye leaking for certain encoding procedures, and spectral crosstalk, limiting the achievable number of detection channels. Moreover, it typically requires several costly excitation light sources. An innovative alternative can be lifetime multiplexing and the discrimination between different encoding fluorophores and carrier beads based on their fluorescence decay kinetics. In order to examine the potential of this approach, dye encoded beads (lifetime encoded surface chemistry) were prepared using several fluorophores from different dye classes and their suitability for lifetime discrimination in a flow was tested in conjunction with a custom designed flow cytometer equipped with a pulsed light source and a fast detector. In a first step, the spectroscopic properties of micrometer-sized dye-stained PMMA beads were studied by means of steady state and time-resolved photoluminescence measurements. For the performance of studies on the practical use of these microbeads in flow cytometry applications, a custom-built demonstrator model for a flow system was employed. Our results demonstrated that lifetime discrimination and simultaneous readout of a ligand fluorescence signal for analyte quantification with a set of dye-stained polymer microbeads at single wavelength excitation is feasible. These studies are expected to pave the road for new applications of fluorescence lifetime multiplexing within the framework of time-domain flow cytometry and bead-based assays. T2 - ANAKON 2017 CY - Tübingen, Germany DA - 03.04.2017 KW - Flow cytometry KW - Fluorescence KW - Life sciences KW - Lifetime encoding KW - Polymer particles PY - 2017 AN - OPUS4-39995 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Hodoroaba, Vasile-Dan A1 - Rades, Steffi A1 - Oswald, F. A1 - Narbey, S. A1 - Radnik, Jörg T1 - Time dependent Analysis of Morphology, Elemental and Chemical Composition of CH3NH3PbI3/TiO2 Solar Cell Layered System N2 - The motivation of this work is to produce thin films perovskite solar cells with constant high light conversion efficiency over time. Loss of efficiency may be caused by structural and/or chemical alterations of the complex layered system. As these changes might take place either in the bulk and/or on the surface of the stratified material, analytical tools addressing both key issues are selected and combined. SEM/EDS combined with XPS were chosen as appropriate methodical approach to characterise perovskite laboratory cells in depth and complementary on top, before and after light exposure. The layered perovskite system investigated here is based on glass covered with fluorine doped tin oxide (FTO), followed by three porous thin films of TiO2, ZrO2 and a thick monolithic carbon. The TiO2 film is subdivided into a dense layer covered by a porous one constituted of nanoparticles with a truncated bipyramidal shape. This layered system serves as the matrix for the perovskite. After infiltration of perovskite solution and annealing, EDS spectral maps on cross-sections of the specimen have been measured. The distribution of relevant elements – Si, Sn, Ti, Zr and C – correlates conclusively with layers visible in the acquired SEM images. Lead and iodine are distributed throughout the porous layers C, ZrO2 and TiO2. Specimens were exposed to ambient daylight for 7 weeks. In a SEM micrograph taken of the cross-section of a sample after illumination, the glass substrate and all layers FTO, TiO2, ZrO2 as well as C are clearly identified. EDS data have been acquired under the same measurement conditions as before the illumination. It was found that several weeks of ambient daylight did not change significantly the qualitative elemental composition of lead and iodine throughout the solar cell system. It was confirmed with EDS that nanoparticles identified in high-resolution SEM micrographs contain mainly Pb and I, indicating these to be the perovskite crystals. However, a time-dependent compositional and chemical altering was observed with XPS for the near-surface region of the outermost ~10 nm after 2 months of illumination. T2 - EMAS 2017 - 15th European Workshop on MODERN DEVELOPMENTS AND APPLICATIONS IN MICROBEAM ANALYSIS and IUMAS-7 Meeting CY - Konstanz, Germany DA - 07.05.2017 KW - Perovskite KW - Layer analytics KW - SEM/EDX KW - XPS KW - Solar cells PY - 2017 AN - OPUS4-40253 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Beckmann, Jörg A1 - Spranger, Holger A1 - Bär, Sylke T1 - THz-TDS-SAFT for the detection of inherent discontinuities in dielectric materials N2 - X-ray computed tomography (CT) model holds only for THz-TDS reconstruction if minor refraction index differences between the inhomogeneities and the surrounding material matrix exist. A Time Domain SAFT algorithm has been developed to overcome the restrictions. THz time domain measurement on representative sample sets with inherent artefacts were performed to use them for the Image reconstructions. The results will be presented and compared with optical surface images of the used test objects to evaluate the SAFT algorithm in relation to the reconstruction quality. T2 - 42nd International Conference on Infrared, Millimeter and THz waves CY - Cancun, Mexico DA - 27.08.2017 KW - THz-time-domain spectroscopy KW - SAFT KW - Tomography PY - 2017 AN - OPUS4-42034 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Mishurova, Tatiana A1 - Thiede, Tobias A1 - Cabeza, Sandra A1 - Bruno, Giovanni A1 - Kromm, Arne A1 - Nadammal, Naresh T1 - The influence of the support structure on residual stress and distortion in SLM Inconel 718 parts N2 - The effect of support structure and of removal from the base plate on the residual stress state in Selective Laser Melted IN718 parts was studied by means of synchrotron X-ray diffraction. The residual stresses in subsurface region of two elongated prisms in as-built condition and after the cutting from the base plate were determined. One sample was directly built on a base plate and another one on a support structure. Also, the distortion on the top surface due to stress release was measured by contact profilometry. High tensile residual stress values were found, with pronounced stress gradient along the hatching direction. In the sample on support stress redistribution took place after removal of the base plate, as opposed to simple stress relaxation for the sample without support. The sample on support structure showed larger distortion compared to sample without support. We conclude that the use of a support decreases stress values but stress relieving heat treatments are still needed. T2 - User Meeting HZB 2018 CY - Berlin, Germany DA - 14.12.2017 KW - Additive manufacturing KW - Selective laser melting KW - Residual stress KW - Synchrotron X-ray diffraction PY - 2017 AN - OPUS4-43460 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Sobol, Oded A1 - Steiner, S. A1 - Albe, K. A1 - Froemling, T. A1 - Unger, Wolfgang T1 - The characterization of oxygen diffusion in (Na1/2Bi1/2)TiO3 piezo-ceramics by Time-of-Flight secondary ion mass spectrometry (ToF-SIMS) N2 - The ferroelectric ceramic NBT and its solid solutions with barium titanate (BT) are examples for the most promising lead free materials to substitute the dominant Pb(Zr,Ti)O3 (PZT). Lead based material should generally be disregarded due to environmental and health reasons. However, there is no class of lead-free piezoelectric materials that can replace PZT entirely. Not only the often inferior ferroelectric properties but also the lack of understanding of the defect chemistry of NBT is still a challenge for the replacement of lead containing piezo-ceramics. Just recently it could be shown by Li et al. that NBT obtains extraordinarily high oxygen ionic conductivity when doped with Mg as acceptor. It was actually expected that doping just leads to a hardening of the ferroelectric properties. However, it became clear that the known defect chemical behavior of PZT cannot be extrapolated to NBT materials. Hence, to gain information on general doping effects a better defect chemical investigation is needed. This is particularly important for the applications with high reliability demands to investigate possible degradation and fatigue mechanisms. In the present work Time-of-flight-secondary ion mass spectrometry (ToF-SIMS) was used in order to observe the influence of different acceptor dopants (Fe, Ni, Al) on the oxygen diffusion in NBT. ToF-SIMS holds the ability to gain a full elemental distribution in a sub-micron resolution and was therefore chosen to provide the essential information on the favorable diffusion paths of oxygen in NBT in dependence of the chosen doping element. 18O was used as a tracer for oxygen as its natural abundance is only 0.2%. The doped NBT samples have been annealed for 5 h at 500°C in a 0.2 bar 18O-tracer atmosphere to be able to detect oxygen ion diffusion. ToF-SIMS investigations were conducted on a ToF-SIMS IV (ION TOF GmbH, Münster, Germany) using a Bi+ primary ion beam (25KeV in collimated burst alignment mode with a beam diameter of ~150 nm) and a Cs+ sputter beam (3KeV). The results illustrate the different impact of dopants on the diffusion properties which is evidence for a highly non-linear dependence on dopant type and concentration. T2 - 21st International Conference on Secondary Ion Mass Spectrometry - SIMS21 CY - Krakow, Poland DA - 10.09.2017 KW - ToF-SIMS KW - NBT KW - Piezoceramics PY - 2017 UR - http://sims.confer.uj.edu.pl/boa_poster.php?id=93 AN - OPUS4-42911 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Sobol, Oded A1 - Steiner, S. A1 - Albe, K. A1 - Froemling, T. A1 - Unger, Wolfgang T1 - The characterization of oxygen diffusion in (Na1/2Bi1/2)TiO3 piezo-ceramics by Time-of-Flight secondary ion mass spectrometry (ToF-SIMS) N2 - The ferroelectric ceramic NBT and its solid solutions with barium titanate (BT) are examples for the most promising lead free materials to substitute the dominant Pb(Zr,Ti)O3 (PZT). Lead based material should generally be disregarded due to environmental and health reasons. However, there is no class of lead-free piezoelectric materials that can replace PZT entirely. Not only the often inferior ferroelectric properties but also the lack of understanding of the defect chemistry of NBT is still a challenge for the replacement of lead containing piezo-ceramics. Just recently it could be shown by Li et al.[1] that NBT obtains extraordinarily high oxygen ionic conductivity when doped with Mg as acceptor. It was actually expected that doping just leads to a hardening of the ferroelectric properties. However, it became clear that the known defect chemical behavior of PZT cannot be extrapolated to NBT materials. Hence, to gain information on general doping effects a better defect chemical investigation is needed. This is particularly important for the applications with high reliability demands to investigate possible degradation and fatigue mechanisms. In the present work Time-of-flight-secondary ion mass spectrometry (ToF-SIMS) was used in order to observe the influence of different acceptor dopants (Fe, Ni, Al) on the oxygen diffusion in NBT. ToF-SIMS holds the ability to gain a full elemental distribution in a sub-micron resolution and was therefore chosen to provide the essential information on the favorable diffusion paths of oxygen in NBT in dependence of the chosen doping element. 18O was used as a tracer for oxygen as its natural abundance is only 0.2%. The doped NBT samples have been annealed for 5 h at 500°C in a 0.2 bar 18O-tracer atmosphere to be able to detect oxygen ion diffusion. ToF-SIMS investigations were conducted on a ToF-SIMS IV (ION TOF GmbH, Münster, Germany) using a Bi+ primary ion beam (25KeV in collimated burst alignment mode with a beam diameter of ~150 nm) and a Cs+ sputter beam (3KeV). The results illustrate the different impact of dopants on the diffusion properties which is evidence for a highly non-linear dependence on dopant type and concentration. 1) Li, M., et al., Nature Materials, 2014. 13(1): p. 31-35. T2 - 21st International Conference on Secondary Ion Mass Spectrometry - SIMS21 CY - Krakow, Poland DA - 10.09.2017 KW - NBT-Piezoceramics KW - ToF-SIMS PY - 2017 UR - http://sims.confer.uj.edu.pl/boa_poster.php?id=93 AN - OPUS4-42863 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Asadujjaman, Asad A1 - Wagner, Sabine A1 - Rurack, Knut A1 - Bertin, Annabelle T1 - Temperature switches “on” and “off” nanoparticle fluorescence in a core/shell/shell architecture N2 - Fluorescent nanoparticles that light “on/off” by applying external stimuli are of particular interest in the fields of sensing, diagnostics, photonics, protective coatings and microfluidics. The current challenge for these materials is for instance to combine fluorescence and its response to a stimulus such as temperature in a precise manner. Here we present such a system based on a core/shell/shell architecture consisting of a silica core with a fluorescent layer and a thermoresponsive shell. In this work the silica core nanoparticles were first coated with a fluorescent shell using surface initiated reversible addition-fragmentation chain transfer (RAFT) polymerization. The fluorescent nanoparticles were then completely engulfed by a switchable protective coating made of thermoresponsive poly(N-isopropylacrylamide). The fluorescence of the nanoparticles could be “switched on” at room temperature and “switched off” with increasing environmental temperature because of the presence of the thermoresponsive layer. Insights into this phenomenon will be given based on temperature dependent fluorescence measurements and dynamic light scattering. T2 - Makromolecular Konferenz CY - Freiburg, Germany DA - 15.02.2017 KW - Thermoresponsive polymers KW - Sensors KW - Core/Shell/Shell PY - 2017 AN - OPUS4-39230 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Bertin, Annabelle A1 - Asadujjaman, Asad A1 - Kent, B. T1 - Temperature Sensitive Aggregation Behavior of Poly(Acrylamide-co-Acrylonitrile) in Water N2 - Thermoresponsive polymers have shown great potential in applications such as bioseparation, drug delivery and diagnostic. Only few thermoresponsive polymers that present an upper critical solution temperature (UCST), i.e. phase separate from solution upon cooling, in a relevant temperature range have been reported so far. Herein, a robust UCST-type copolymer of acrylamide (AAm) and acrylonitrile (AN) (poly(AAm-co-AN)) was prepared by reversible addition fragmentation chain transfer (RAFT) polymerization and its thermo-induced aggregation behavior in aqueous media was studied. We propose a model for the temperature-induced aggregation behaviour of UCST-type poly(AAm-co-AN) copolymer in aqueous solution on the basis of turbidity measurements, SLS, DLS, SANS and cryo-TEM. T2 - German Physical Society - Spring Meeting 2017 CY - Dresden, Germany DA - 19.03.2017 KW - Thermoresponsive polymers KW - UCST-type copolymer PY - 2017 AN - OPUS4-39465 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Detjens, Marc A1 - Hübert, Thomas A1 - Tiebe, Carlo A1 - Banach, Ulrich T1 - Temperature influence on coulometric trace humidity measurement N2 - Coulometric sensors were tested in humidified synthetic air at various gas temperatures. Generated frost point temperature in the gas ranged from -30 °C to -60 °C and were measured by coulometric sensors and in addition by a calibrated dew point hygrometer. The gas temperatures, which were measured by a calibrated Pt100 sensor, were set to -20 °C, 0 °C, 23 °C, 40 °C, 50 °C, and 60 °C during the experiments. Empiric nonlinear functions were calculated between the humidity and the sensor signal. In comparison to the measured signals at 23 °C, the sensor signals were lower at the other gas temperatures. Measurements at 60 °C showed indistinct results due to a great signal noise. The response behavior of the sensors was similar at 23 °C, 40 °C and 50 °C. In contrast to that, the sensors reacted slowly at a gas temperature of -20 °C and 0 °C. In summary, with coulometric sensors it was possible to measure continuously trace humidity with an expanded uncertainty below 2 K. T2 - IEEE Sensors 2017 CY - Glasgow, Scotland, UK DA - 30.10.2017 KW - Coulometric sensors KW - Trace humidity measurement KW - Temperature influence KW - Chemical reaction KW - Response behavior PY - 2017 AN - OPUS4-42756 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER - TY - CONF A1 - Kulow, Anicó A1 - de Oliveira Guilherme Buzanich, Ana A1 - Radtke, Martin A1 - Reinholz, Uwe A1 - Riesemeier, Heinrich A1 - Streli, Christina T1 - S²XAFS: A new experimental setup for time-resolved X-ray absorption fine structure spectroscopy in a 'single shot' N2 - A newly developed EXAFS setup is presented. It enables both time- and spatially resolved EXAFS information simul-taneously in a single shot. First tests of this setup were performed at the BAMline @ BESSY-II (Berlin, Germany). A primary broadband beam generated by a filter/X-ray-mirror combination passes through the sample and is then dif-fracted by a convexly bent Si (111) crystal. This results in a divergent beam which is collected by an area sensitive detector, in a θ-2θ-geometry. Beside tests on metal foils the first in situ measurements were successfully carried out. The case-study deals with research on Zn-based Metal-Organic-Frameworks (MOF) with medical/pharmaceutical applications. This hot topic of MOFs research concerns drug delivery and encapsulation of therapeutically relevant proteins (e.g. BSA). Questions like how does a certain protein influences the coordination of Zn can be answered with this new setup. We were able to track structural changes within a 1s time resolution. T2 - CSI XL CY - Pisa, Italy DA - 11.06.2017 KW - XAFS KW - Time-resolved KW - Dispersive KW - In-situ measurement PY - 2017 AN - OPUS4-41052 LA - eng AD - Bundesanstalt fuer Materialforschung und -pruefung (BAM), Berlin, Germany ER -