Analytische Chemie
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Permeability estimation from spectral induced polarization (SIP) measurements is based on a fundamental premise that the characteristic relaxation time (t) is related to the effective hydraulic radius (reff) controlling fluid flow. The approach requires a reliable estimate of the diffusion coefficient of the ions in the electrical double layer. Others have assumed a value for the diffusion coefficient, or postulated different values for clay versus clay-free rocks. We examine the link between t and reff for an extensive database of sandstone samples where mercury porosimetry data confirm that reff is reliably determined from a modification of the Hagen-Poiseuille equation assuming that the electrical tortuosity is equal to the hydraulic tortuosity. Our database does not support the existence of 1 or 2 distinct representative diffusion coefficients but instead demonstrates strong evidence for 6 orders of magnitude of variation in an apparent diffusion coefficient that is well correlated with both reff and the specific surface area per unit pore volume (Spor). Two scenarios can explain our findings: (1) the length-scale defined by t is not equal to reff and is likely much longer due to the control of pore surface roughness; (2) the range of diffusion coefficients is large and likely determined by the relative proportions of the different minerals (e.g. silica, clays) making up the rock. In either case, the estimation of reff (and hence permeability) is inherently uncertain from SIP relaxation time.
Zur Bestimmung des Feuchtezustands und insbesondere der Belegereife von Estrichfußböden kommen in Deutschland zerstörende Prüfverfahren zum Einsatz, die eine punktuelle Probenahme erfordern. Hierbei ergeben sich immer wieder Fehlinterpretationen, da zum einen die Probenahme selbst zu einer Veränderung des Feuchtezustands führt und zum anderen, weil die Verfahren an sich mitunter ungenau sind (z.B. abhängig von der Estrichzusammensetzung). Zusammen mit vier Forschungsinstituten und dem Industriepartner Bosch wurden an der BAM zerstörungsfreie Prüfverfahren auf deren Tauglichkeit zur Estrichfeuchtemessung untersucht und mit den herkömmlichen zerstörenden Verfahren verglichen.
Für diesen Versuch kamen verschiedene geophysikalische Verfahren zum Einsatz, darunter Nuklear Magnetische Resonanz (NMR), elektrische Widerstandsmessungen und Impulsradar (GPR). Es wurden neun verschiedene Estrichsorten hergestellt und während der Trocknungsphase bei Konstant-Normklima gelagert. Diese wurden sowohl zerstörend als auch zerstörungsfrei mit den o. g. Verfahren untersucht. Gleichzeitig wurden die Masseänderungen der Proben zur Bestimmung des integralen Feuchtehalts aufgezeichnet.
Die Ergebnisse zeigen zum einen, dass das Abtrocknungsverhalten von zementgebundenen Estrichen grundsätzlich unterschiedlich von dem anhydritgebundener Estriche ist. Während sich bei ersteren zügig ein deutlicher Feuchtegradient über die Höhe der Proben einstellt, verläuft dieser bei der zweiten Probengruppe sehr flach. Dies lässt sich vor allem in den NMR Daten räumlich hochaufgelöst nachvollziehen - die Datenakquise erfolgte mit einer NMR MOUSE PM 25. Ein ähnliches Bild ergibt sich auch aus den elektrischen Widerstandsmessungen, die mittels sog. Multi-Ring-Elektroden (MRE) durchgeführt wurden. MRE bezeichnen als Vertikalprofil angeordnete Ringelektroden mit einem Abstand von ca. 1-2 mm, zwischen denen jeweils Zwei-Punkt Widerstandsmessungen durchgeführt werden. Bei sehr geringen Feuchtegehalten (z.T. auch um die Belegereife) waren mit dieser Methode jedoch wegen der zu hohen Übergangswiderstände nur bedingt Messungen möglich. Im Gegensatz zu NMR und MRE sind mit dem Radarverfahren (2 GHz Antenne) keine tiefenbezogenen Aussagen möglich. Jedoch lässt sich über eine Amplitudenauswertung von direkter und an der Rückwand reflektierter Welle teilweise eine Aussage über Restfeuchtigkeit im Volumen treffen. Ebenso zeigt die Laufzeitdifferenz der beiden Wellen eine starke Abhängigkeit vom Feuchtegehalt.
In Germany there is an existing built infrastructure worth about 50 trillion Euros. The expected lifetimes of individual structures are up to 100 years. Considerable costs (annually about 35 billion Euros, the trend continues upwards) are involved in order to maintain and rehabilitate both residential as well as transportation infrastructure buildings. Most damages we observe on our built infrastructure are moisture-induced processes. Consequently reliable moisture measurement tools a highly needed for meaningful building diagnosis investigations. The optimal moisture measuring technique would be non-destructive, fast, repeatable, reliable, independent of steel in the vicinity, the surface condition or possible salt loads of the material under test. Since this is unfortunately not the case for any non-destructive method, it is often very difficult to decide for users which method to use for the particular testing problem. The only standardized methods in Germany are the “direct” and destructive Darr- and the CM tests. Although they can be highly accurate (when handled with care during the sampling), they deliver only punctual information and cannot be used for monitoring. The other, non-destructive methods are based on the change in humidity-dependent physical material properties. The underlying physics, their particular advantages and disadvantages are discussed in this paper.
Permeability estimation from spectral induced polarization (SIP) measurements is based on a fundamental premise that the characteristic relaxation time (t) is related to the effective hydraulic radius (reff) controlling fluid flow. The approach requires a reliable estimate of the diffusion coefficient of the ions in the electrical double layer. Others have assumed a value for the diffusion coefficient, or postulated different values for clay versus clay-free rocks. We examine the link between t and reff for an extensive database of sandstone sampleswhere mercury porosimetry data confirm that reff is reliably determined from a modification of the Hagen-Poiseuille equation assuming that the electrical tortuosity is equal to the hydraulic tortuosity. Our database does not support the existence of 1 or 2 distinct representative diffusion coefficients but instead demonstrates strong evidence for 6 orders of magnitude of variation in an apparent diffusion coefficient that is well correlated with both reff and the specific surface area per unit pore volume (Spor). Two scenarios can explain our findings: (1) the length-scale defined by t is not equal to reff and is likely much longer due to the control of pore surface roughness; (2) the range of diffusion coefficients is large and likely determined by the relative proportions of the different minerals (e.g. silica, clays) making up the rock. In either case, the estimation of reff (and hence permeability) is inherently uncertain from SIP relaxation time.
The surface modification of nanometer- and micrometer-sized particles with polyethylene glycol (PEG) ligands of varying length is a very common strategy to tune their hydrophilicity and biocompatibility, minimize unspecific interactions, improve biofunctionalization efficiencies, and enhance blood circulation times. Nevertheless, simple methods for the quantification of PEG ligands are rare. This is similarly true for the spectroscopic characterization of lanthanide-doped upconverting nanoparticles (UCNPs), novel near infrared (NIR)-excitable nonlinear fluorescence reporters for bioanalysis and theranostics, providing background-free multiple narrow emission bands in the visible and NIR, excellent photostability, and long luminescence lifetimes.
We present here a simple method for the determination of the number of PEG ligands on nanomaterials and screening methods for the fast identification of nonradiative deaction pathways in UCNPs.
The surface chemistry / functionalization of nanomaterials and microparticles largely controls the stability of these materials as well as their solubility and subsequent biofunctionalization and their interactions with biological systems. Moreover, in the case of some nanomaterials like semiconductor quantum dots or lanthanide-based upconversion nanocrystals, the ligand shell strongly affects their optical properties, e.g., via passivation of surface states and traps that favor luminescence quenching or the protection of surface atoms from quenching water molecules. This renders analytical methods for the quantification of surface groups like functionalities very important. Targets of broad interest are here amino, carboxyl, alkine and maleimide groups used for common bioconjugation reactions and typical ligands like thiols and polyethylene glycol (PEG) molecules of varying length, used for the tuning of material hydrophilicity and biocompatibility, minimization of unspecific interactions, prevention of biofouling, and enhancement of blood circulation times as well as surface-bound biomolecules like streptavidin or other biomolecules relevant e.g., for diagnostic assays. Here, we focus on simple optical methods relying on standard laboratory instrumentation, validated by method comparison and/or mass balances and present examples for their use for the characterization of different types of nanomaterials and microparticles.
Luminescence-based detection methods, ranging from fluorescence spectroscopy for photophysical and mechanistic studies over sensing applications, chromatographic separation techniques and the microarray technology with fluorescence detection to fluorescence microscopy, flow cytometry, single molecule spectroscopy, and molecular imaging to integrating sphere spectroscopy, are among the most widely used methods in the life and material sciences. This is due to e.g., their unique sensitivity enabling the detection of single molecules, potential for multiplexing, ease of combination with spatial resolution, and suitability for remote sensing. Many of these advantages are closely linked to the choice of suitable molecular and nanoscale fluorescent reporters, typically required for signal generation. This includes organic dyes without and with sensor function, fluorophore-encoded polymeric and silica nanoparticles as well as nanocrystalline systems like semiconductor quantum dots and upconversion phosphors, emitting in the visible (vis), near-infrared (NIR), and IR (infrared). Current challenges present the environment sensitivity of most fluorophores, rendering fluorescence spectra, measured intensities/fluorescence quantum yields, and fluorescence decay kinetics matrix-dependent, and instrument-specific distortions of measured fluorescence signals that need to be considered for quantification and comparability of data, particularly fluorescence spectra.
Here, current applications of luminescence-based methods and different types of reporters will be presented. In this context, suitable spectroscopic tools for the characteri-zation of the optical properties of fluorescent reporters and fluorophore-encoded microparticles, analytical tools for the determination of the surface chemistry of different types of particles, and different multiplexing strategies will be discussed.
Fluorescent particles like nm- and m-sized polymeric beads doped or labeled with different types of fluorophores and nanocrystalline systems like quantum dots and upconversion phosphors emitting in the visible (vis), near-infrared (NIR), and IR (infrared) region are of increasing importance as fluorescent reporters for bioanalysis and medical diagnostics. The assessment and comparison of material performance and the development of rational design strategies for improved systems requires suitable spectroscopic tools for the determination of signal-relevant optical properties and analytical tools for the determination of the number of surface groups, ligands, biomolecules and /or fluorophores per bead. In this respect, suitable spectroscopic tools for the characterization of the optical properties of such materials like photoluminescence quantum yields and brightness values and the determination of their surface chemistry are introduced. This includes integrating sphere setups for absolute measurements of fluorescence quantum yields of liquid and solid, transparent and scattering materials in the wavelength region of 350 nm to 1600 nm at varying excitation power densities for the study of multi-photon processes and simple optical assays, validated by comparison with established analytical techniques relying on different detection principles. Here, different examples for the optical and analytical characterization of different types of nanoscale reporters are presented.
Biological systems exhibit a very high complexity, because they consist of various cell populations showing heterogenic characteristics. Therefore the individual analysis of single cells is important to understand cellular processes as well as their function in a cell system. Especially investigation in the question about what is biological variability and what is a substantial difference between two cells of the same type (which might lead to dysfunction or disease) is of high interest. Today improved spatial and temporal resolution enable the use of laser ablation inductively coupled mass spectrometry (LA-ICP-MS) for element microscopy of single cells. Next to the characterization of natural trace elements the introduction of artificial metal labels into cells is of high interest. Element labeling of cell compartments and/or proteins allows its simultaneous analysis and localization within a cell via element microscopy. Two fast and simple metal staining procedures of adherent cells for identification of single cells via LA-ICP-MS at sub micrometer resolution are presented. An Iridium-intercalator is utilized to stain the cell nuclei whereas the whole cell is stained by maleimido-mono-amide-DOTA-complexes (mDOTA) loaded with lanthanide(III) isotope ions. The metal staining procedures allow the visualization of single cells by element microscopy independent of a superposition of analyte’s 2D element intensity profile with a prior taken bright field image of the sample.
Photoluminescence techniques are amongst the most widely used tools in the material and life sciences, with new and exciting applications continuously emerging, due to their many advantages like comparative ease of use, unique sensitivity, non-invasive character, and potential for multiplexing, remote sensing, and miniaturization. Drawbacks are , however, signals, that contain unwanted wavelength- and polarization contributions from instrument-dependent effects, which are time-dependent due to the aging of instrument components, and difficulties to measure absolute fluorescence intensities. Thus, there is a considerable need for standards for intensity, spectral, and temporal fluorescence quantities to meet the increasing need for instrument performance validation and global trends to harmonize physicochemical measurements. In this respect, instrument calibration strategies together with different types of fluorescence standards are presented as well as design concepts for robust, easy-to-use, and format-adaptable fluorescence standards useable for the determination of different fluorescence parameters and a broad variety of fluorescence techniques.
Industrial quality control (QC) nowadays requires the visualization of surface modifications from the macro-scopic to the microscopic or even nanoscopic scale. This is a prerequisite to the evaluation of functionality and reliability, the detection of defects and their separation of artefacts. The diversity of applications ranges from low-E glazings and solar panels, micro- and optoelectronics, micro- and smart devices to sensor-on-chip and lab-on-chip systems [1]. Optical microcopy (light, confocal laser scanning, white light interference) as established QC-tool is operated at normal incidence, i.e. p- and s-polarization are undistinguishable. Either light-intensity in terms of grey scale and colour or intensity-correlated effects of phase shifts are used. In case of ellipsometry, operated at oblique incidence, p- and s-polarization matter, and amplitude ratios and phase shifts upon reflection are measured. Hence, information content must be much higher.
The visualization of surface modifications may be very challenging for coating/substrate systems of either al-most identical optical constants, e.g. transparent films on substrates of the same material, or minor film thick-ness, substance quantity and affected area, e.g. ultra-thin or island films. Ellipsometry gives access to the con-trast of intensity (I), amplitude ratio (Ψ), and phase shift (Δ) with nanometer-scaled vertical and micrometer-scaled lateral sensitivity, one is able to identify tiny changes within an unmodified surface. As both mapping ellipsometry (ME) and imaging ellipsometry (IE) are operated in the optical far-field, surface inspection is also possible on the macroscopic scale. Near the Brewster-angle of the bare, undamaged, clean, and fresh substrate, the contrast to add-on and sub-off features is superior.
Fig. 1 shows three examples of ellipsometric imaging, i.e. a thin SnO:Ni film on SiO2/Si (Fig. 1a), a dried stain of an anti-body solution on cyclo-olefin-polymer (COP) shown in Fig. 1b, and a polyimide film residue on SiO2/Si (Fig. 1c). For all of these examples, ellipsometry provides much better contrast between substrate and surface modification than optical microscopy, sometimes primarily caused by the oblique incidence (Figs. 1a and 1c), in other cases related to the phase sensitivity of ellipsometry (Fig. 1b). Other examples are laser surface modifications and the corrosion of glass. In these cases, optical microscopy and IE yield to similar results, how-ever only ellipsometry gives access to modelling.
Further investigated coating/substrate systems are 100Cr6 steel, native oxide on silicon, borosilicate glass, and the polymer polycarbonate with deposited films of graphene and ta-C:H, printed and dried pattern of liquids such as water, cleaning agents, and dissolved silicone. Besides imaging ellipsometry, referenced spectral ellipsometry (RSE) has been applied, combining the advantages of both optical microscopy (fast measurement) and ellipsometry (high sensitivity to tiny modifications).
Der einwandfreie Zustand der Radsätze von Schienenfahrzeugen ist von größter Bedeutung für den sicheren Betrieb. Die Radsatzwellen werden durch eine große Zahl von Lastwechseln individuell unterschiedlich beansprucht. Dabei spielen viele Einflüsse wie äußere statische und dynamische Lasten, innere Lasten aufgrund von Unwuchten und inneren Spannungen und Umweltbedingungen entscheidende Rollen. Eine regelmäßige Prüfung ist daher obligatorisch.
BTD entwickelt im Rahmen eines MNPQ-Projektes in Kooperation mit der BAM eine Phased Array Technik zur automatisierten Prüfung von Radsatzwellen im eingebauten Zustand. Die schwierigen Ankoppelbedingungen aufgrund der begrenzten Zugänglichkeit, der komplexen Geometrie und möglicherweise vorhandener Farbschichten und Schmutz auf der Radsatzwelle stellen hierbei große Herausforderungen dar. Um diesen zu begegnen, werden neben optimierten Prüfköpfen, einer in die Wasservorlaufstrecke integrierten akustischen Linse und einer speziellen Ankoppeltechnik auch Signalverarbeitungsalgorithmen eingesetzt.
Die Darstellung der Signalverarbeitung ist der Schwerpunkt dieses Beitrages. Mit Hilfe von Messdatensätzen präparierter Testwellen werden verschiedene Algorithmen erprobt und hinsichtlich der Stabilität, dem Verhalten bezüglich der Ankoppelschwankungen und veränderter Wellengeometrien und der Fähigkeit zur automatischen Unterscheidung von Fehler- und Formanzeigen bewertet. Letztlich wird die beste Lösung im entwickelten Prüfsystem eingesetzt.
In the last two decades automated ultrasonic inspection devices took over a lot of applications that prior have been carried out using manual inspection with the evaluation of A-scans only. In parallel phased array systems have been developed and brought to the market which offer detailed and fast control over the sound field. When applying automated inspection phased array systems for UT measurements imaging of the recorded data in combination with the probe positioning data is used for the evaluation of inspections. B-Scan, C-Scan and S-Scan images are typically used with this setup.
For more sophisticated applications with linear arrays echo tomography and syntethic aperture focusing technique (SAFT) are well known methods and often applied for high resolution image reconstruction. Since channel count of phased array systems is constantly rising, matrix arrays with up to 256 elements entered the market. Signal processing in the matrix domain became 3D. Since some years the Total Focusing Method (TFM) is an additional imaging tool for these type of application. It is based on the Full Matrix Capture (FMC) using the elements of phased array probes as separate transmitters and receivers.
In this contribution we discuss the common ground of SAFT and TFM as well as the differences between these imaging tools. The combined use of automated inspection, matrix arrays and signal processing for high resolution measurements is a challenging task where a very long parameter list has to be taken into account. Under which conditions which elements of the full matrix should be taken for the reconstruction for best results?
Based on examples taken from measured and simulated echo signals it will be shown how image resolution can be optimized in dependence of different parameters like the distance between transmitters and receivers and their directivity patterns, the depth of echo source and the specimen geometry.
Most VVOC were rarely considered in the evaluation of construction products. (Salthammer, 2014) In Germany this will change because the latest version of the German AgBB scheme for health evaluation (2015) now include VVOC, e.g. ethyl acetate and ethanol. In this study selected compounds were tested with the procedure described in ISO 16017 and a method for measuring VVOC with thermal desorption was developed.
Three different adsorbents Tenax TA, Carbograph 5TD and Carbopack X were tested to analyse VVOC according to ISO 16017. For the tested VVOC, Carbograph 5TD showed the best results under the chosen analytical conditions.
Gas sensors are an important tool in various areas for example in industrial process control as well as Gas sensors are an important tool in various areas for example in industrial process control as well as safety applications or in research. A useful gas detector should be selective, precise, stable and cost-effective. In the present research a surface based gas detection technique is investigated using the SPR effect with ellipsometric readout. This technique is called surface plasmon resonance enhanced ellipsometry (SPREE).
The sensor consists of a gold layer (40 nm) top-coated with a doped metal-oxide (M:SnOₓ,
5 nm). The coating is added by magnetron sputtering with doped targets with different doping concentrations. It could be shown that, without the top-coating, these type of sensors can detect various gases, e.g. CO, H2, O2, O3, He, N2, with sensitivities down to the ppm range (in air).
The goal of the present study is to characterize the additional coating materials in dependence of the coating conditions. With the help of the doped-metal oxide, the sensitivity increases dramatically by a factor of 100. Additionally, a selectivity for specific gases is observed which depends on the doping conditions of the coating. Changing the properties of the plasma coating process and the doping metal gives access to a variety of different layers and enables us to find the best conditions.
Die quantitative Bestimmung der Haftfestigkeit von Beschichtungen ist von entscheidender Bedeutung sowohl für die Entwicklung als auch für die Qualitätssicherung. In einer Vergleichsstudie zur Haftfestigkeit von optischen und ophthalmischen Schichten wurde mit Hilfe der Zentrifugentechnologie der Einfluss verschiedener Parameter (Substratdicke, Oberflächenvorbehand-lung, Haftvermittler) auf die Haftfestigkeit optischer Schichten auf silikatischen und ophthalmischer Schichten auf polymeren Substraten untersucht.
Zur Bestimmung der Haftfestigkeit in der physikalisch korrekten Dimension Kraft pro Fläche im Stirnabzug stehen die Ein-Proben-Prüfung mit der Zugprüfmaschine und die Mehr-Proben-Prüfung mittels Zentri- fugentechnologie zur Verfügung. Die Zentrifugentechnologie wurde ausgewählt, da die Prüfung von bis zu acht Proben unter nahezu identischen Versuchsbedingungen und somit eine statistisch gesicherte Bestimmung der Haftfestigkeit möglich sind.
Es konnte nachgewiesen werden, dass die Substratdicke einen erheblichen Einfluss auf die gemessene Haftfestigkeit hat. Dies entspricht den Erwartungen, da es sich bei der Haftfestigkeit um eine System- eigenschaft des Schicht-Substrat-Systems handelt. Bei den Delaminationsbrüchen (DF) konnte zwischen Delamination des metallischen Reflektors (DF-R) und Delamination des Dielektrikums (DF-D) unter- schieden werden. Im Fall hinreichender Haftfestigkeit der Beschichtung traten auch Adhäsionsbrüche am Interface zum und Kohäsionsbrüche im Klebstoff auf. Nachfolgende Untersuchungen werden sich mit alternativen Klebstoffen und weiterentwickelten Fügestrategien befassen.
Quantification of rock structures with high resolution X-Ray μ-CT for laboratory SIP measurements
(2016)
Spectral Induced Polarization (SIP) measurements are used in many different ways to characterize natural rocks and soils. Main foci of interest are the enhanced characterization of the causes of IP-effects in clastic rocks (especially sandstones), the interactions between the matrix-fluid-system and within the electrical double layers as well as the correlation with “classical” petrophysical parameters, such as specific surface area, permeability, mercury intrusion capillary pressure (MICP) and others. Nevertheless, for all of these investigations, knowledge of the inner structure of the sample material is essential in order to create reliable and validated models as well as to interpret and to assess the data most completely. Unfortunately, many of the methods used, to get access to the inner structure of rocks are destructive (e.g. MICP, thin sectioning, etc.) and the valuable sample is lost. In addition, data is either of volume integrated nature or only available for the 2D case and the usage of sister cores does not necessarily lead to reliable results. In this paper, the authors showcase the possibilities of non-destructive and three dimensional X-ray computed tomography and of enhanced image analysis capabilities for the quantification of rock structures at the pore scale.
The reliability of wheel set axle testing is of high importance because small discontinuities caused during manufacturing or rock fall impacts during operation might cause growing cracks during the operation load cycles. While most of the axles are tested by automated UT-systems today, the basic education of railway NDT operators is still manual testing providing the basic understanding and skills for the operators. In Germany it is a common rule that NDT operators in the railway branch need to refresh their knowledge and skills every five years including a refresh examination. The testing results from these exercises and from a parallel round robin test have been sampled at the DGZfP Railway Education Centre in Wittenberge for a period of about 5 years. The results of the operators written in test record sheets were compared with the “true” test crack or notch position in the axles used for examination. In this way the testing results could be categorized into “hits” and “misses” and the “hits” were further evaluated due to correct position and adequate amplitude height. Considering some thousand indications documented by the operators during the refresh examination and comparing transition bow, shaft and seat it was a highlight to see that the operators reach their best detection rate in the transition bow of the wheel axle set while this is often the most difficult part concerning the UT-echoes. Fortunately this is due to their raised awareness in the transition bow region because this is the most dangerous region with respect to fracture mechanics.
For two selected axles the experimental set up of 45° and 70° inward and outward UT-testing were also simulated showing clearly the difficulties of the UT-echoes detection of some specific test defects.
Der einwandfreie Zustand der Radsätze von Schienenfahrzeugen ist von größter Bedeutung für den sicheren Betrieb. Die Radsatzwellen werden durch eine große Zahl von Lastwechseln individuell unterschiedlich beansprucht. Dabei spielen viele Einflüsse wie äußere statische und dynamische Lasten, innere Lasten aufgrund von Unwuchten und inneren Spannungen und Umweltbedingungen entscheidende Rollen. Eine regelmäßige Prüfung ist daher obligatorisch. BTD entwickelt im Rahmen eines MNPQ-Projektes in Kooperation mit der BAM eine Phased Array Technik zur automatisierten Prüfung von Radsatzwellen im eingebauten Zustand. Die schwierigen Ankoppelbedingungen aufgrund der begrenzten Zugänglichkeit, der komplexen Geometrie sowie Farbschichten und Schmutz auf der Radsatzwelle stellen hierbei große Herausforderungen dar. Zu deren Bewältigung werden neben optimierten Prüfköpfen, einer in die Wasservorlaufstrecke integrierten akustischen Linse und einer speziellen Ankoppeltechnik auch Signalverarbeitungsalgorithmen eingesetzt. Die Darstellung der Signalverarbeitung ist der Schwerpunkt dieses Beitrages. Mit Hilfe von Messdatensätzen präparierter Testwellen werden verschiedene Algorithmen erprobt und hinsichtlich der Stabilität, dem Verhalten bezüglich der Ankoppelschwankungen und veränderter Wellengeometrien und der Fähigkeit zur automatischen Unterscheidung von Fehler- und Formanzeigen bewertet. Letztlich wird die beste Lösung im entwickelten Prüfsystem eingesetzt.
Die regelmäßige Überprüfung von Eisenbahnradsatzwellen auf betriebsbedingte Schädigungen ist ein fester Bestandteil des Instandhaltungskonzeptes von Eisenbahnfahrzeugen. Insbesondere bei hohen Achslasten und hohen Rotationsgeschwindigkeiten ist eine detaillierte regelmäßige Prüfung notwendig. In den letzten Jahren wurden für diese Prüfaufgabe mechanisierte Ultraschallprüfsysteme entwickelt, erfolgreich eingeführt und etabliert. Für eine Weiterentwicklung dieser Technologie stehen die Themen Erhöhung der Auflösung, Reduzierung von Oberflächen- und Störeinflüssen, Verkürzung von Prüfzeiten, Verbesserung der POD, Verlängerung von Inspektionsintervallen, Vereinfachung der Auswertung und die Möglichkeit der Durchführung von Analyseprüfungen im Vordergrund. Es werden Ansätze und neue Konzepte zur Lösung dieser Herausforderungen vorgestellt.
Moisture measurement methods
(2016)
Moisture can cause imperfect sealings, faulty roof constructions, cracks and other kind of damages. For measuring the moisture in construction materials like concrete and screed, there are destructive(direct) and non-destructive(indirect) methods, that can be used. This presentation gives an overview and a comparison of these methods.
There is an increasing interest in optical reporters like semiconductor quantum dots and upconversion nanocrystals with emission > 800 nm for bioanalysis, medical diagnostics, and safety barcodes. Prerequisites for the comparison of material performance, the mechanistic understanding of nonradiative decay channels, and the rational design of new nanomaterials with improved properties are reliable fluorescence measurements and validated methods for the assessment of their surface chemistry. The latter is of special relevance for nanocrystalline emitters, where surface states and the accessibility of emissive states by quenchers largely control accomplishable photoluminescence quantum yields and hence, signal sizes and detection sensitivities from the reporter side. Here, we present the design of integrating sphere setups for the excitation power density-dependent absolute measurement of emission spectra and photoluminescence quantum yields in the wavelength region of 350 to 1600 nm and results from spectroscopic studies of semiconductor quantum dots and upconversion nanocrystals of different size and surface chemistries in various environments. Subsequently, examples for simple approaches to surface group and ligand analysis are presented.
Here, we present an overview of the research activities of division Biophotonics concerning the design and (bio)analytical application of molecular and nanoscale functional chromophores for e.g., biomarker analysis including methods for the reliable determination of their application relevant properties. This includes the absolute determination of their brightness and photoluminescemce quantum yield, determining the signal size from the material side, as well as the development of fluorescence standards for such measurements and instrument calibration strategies, thereby providing important prerequisites for the comparison of material performance, the mechanistic understanding of nonradiative decay channels, and the rational design of new optical reporters. Moreover, for particle-based systems, ranging from nm-sized semiconductor quantum dots to m-sized polymeric and silica beads, simple optical methods and assays for the assessment of their surface chemistry are presented, which enable the quantification of the number of total and derivatizable surface functionalities, ligands per particle and particle-bound biomolecules. In addition, validation concepts for such methods are introduced utilizing method comparisons, multimodal and cleavable probes.
Im Bauwesen werden Polymerbeschichtungen häufig eingesetzt um einerseits ein bestimmtes Aussehens zu schaffen oder andererseits das Bauteil vor Alterung, Verschleiß oder Schädigung zu schützen. Bei praktisch allen Arbeitszielen ist deren Wirkung von der eigens dafür definierten Schichtdicke der Polymerbeschichtung abhängig. Daher wird die Dicke der Beschichtung nach erfolgtem Schichtauftrag überprüft. Für den in diesem Zusammenhang anspruchsvollen mineralischen Untergrund Beton stehen bislang allerdings nur zerstörende Prüfverfahren zur Verfügung. Aus diesem Grund soll im Rahmen des Projektes in Kollaboration mit der IBOS GmbH ein auf aktiver Thermografie basierendes Verfahren sowie ein Gerät für den vor-Ort-Einsatz entwickelt werden, mit dessen Hilfe eine zerstörungsfreie Schichtdickenbestimmung möglich ist.
Der Vortrag gibt einen kurzen Überblick über die Schichtdickenbestimmung mit Hilfe aktiver Thermografie und erläutert die speziellen Herausforderungen an die Thermografie für die in diesem Projekt zu charakterisierenden Polymerwerkstoffe. Zudem wird auf die Anforderungen an die zu entwickelnde Methode, den aktuellen Stand der Entwicklung sowie auf erste Ergebnisse des Projektes eingegangen.
So far, only destructive measurement techniques are available for thickness determination of polymer based surface protection systems for concrete surfaces. Pulse thermography appears to be well suited for non-destructive thickness evaluation in these systems. Here, we present first results of the development of a respective measurement and analysis procedure. Since surface protection systems consist of a number of layers, a model for the calculation of the surface temperature of a multi-layer structure on an infinite (concrete) substrate in pulse thermography setup was developed. It considers semitransparency of the upmost layer and thermal losses at the surface. It also supports the use of an arbitrary temporal shape of the heating pulse to properly describe the measurement conditions for different heat sources. First experimental results regarding the verification of the model are presented.
Funding by the Federal Ministry for Economic Affairs and Energy is gratefully acknowledged.
In this contribution, two large-area EDS detectors were tested according to the procedure proposed by Procop et al. (2015). In a first step, the optimal working distance (WD) in the two different SEM chambers was determined by moving the sample stage in the Z direction and monitoring the count rates at a magnification of 10,000 and a field of view of 25.6 µm. The WD at which the highest intensity was measured was selected as the optimal position, corresponding to the crossover between the EDS detector optical axis and electron beam optical axis. Next the Cu Kα peak was measured at different relative EDS positions while it was partially removed from the fully inserted position. The spectrum at each location was collected for 10 sec using the highest pulse rate and intermediate current to minimize pile up effects. The ‘inverse squared normalized intensities vs. relative EDS position’ used to extract the true detector – specimen distance shows a non-linear relationship even at the minimal relative positions, which indicates shadowing due to obstruction or use of an unsuitable and/or off-centered collimator. The normalized count rates measured as a function of the EDS distances, results in a too low GCE (too low true solid angles) for both tested detectors. The source of losses of signal was shadowing caused by collimators.
Safe innovation & sustainable production with MNMs need that we:
Understand risks and benefits (diagnostic, assessment)
Identify and implement risk reduction strategies (manage)
Communicate on residual risks (acceptance)
Huge knowledge on characterization, hazards, diagnostic (science)
Little effective use of it for operational risk management (expertise)
Objectives of the centre:
Bridge the gap between research and application (public, private),
Bridge the gap between knowledge on risks and risk management,
Balance between Science and Appliance,
in a sustainable way:
Efficient & Sustainable structure
Collective, harmonized, shared expertise
EU scale, internationally connected.
Characterization of bio-molecular surfaces and liquids by means of reference-free X-ray spectrometry
(2016)
An increasing field of application for X-ray spectrometry and related analysis techniques is the investigation of tailor made functional surfaces modified by organic molecules. For a detailed understanding and further development of such functionalized surfaces, a quantitative determination of the surface density of molecular species or even specific functional groups is required. By means of reference-free X-Ray Fluorescence (XRF) spectrometry such customized surfaces can be analyzed quantitatively, when using specific marker elements. A chemical analysis of molecular bonds can be accomplished by X-Ray Absorption Spectroscopy in the Near-Edge region (NEXAFS). Especially in the soft X-ray range an access to relevant light elements like carbon C, nitrogen N and oxygen O is possible. Especially, the characterization of liquids and solid-liquid interfaces aiming at the determination of bio-molecular moieties (functional groups) is of great interest. The characterization of such systems requires the analysis of bio-molecules in their liquid environment. For the understanding of (biomolecular) reactions and binding processes the verification and quantification of biomolecule immobilization is essential. However, the analysis in the soft-X-ray range involves a higher experimental effort. In this contribution various successful applications of the characterizations of organofunctionalized surfaces, solid-liquid interfaces and liquids containing bio-molecular species by means of reference-free X-ray spectrometry will be presented. The experiments were performed at the plane-grating monochromator beamline (PGM-U49) in the soft X-ray range at the synchrotron radiation facility BESSY II. Using calibrated instrumentation and a quantification approach based on atomic fundamental parameters a quantitative access without any calibration sample or reference material is possible. In a complementary analysis by X-Ray Photoelectron Spectroscopy (XPS) and fluorescence measurements based on laserexcitation in the optical light spectrum the functional-group density of silane monolayers were determined. Here, the nitrogen atoms of the head-group of the label molecule employed could be used as specific marker for the reference-free quantitative XRF analysis and is used for traceable calibration of XPS and fluorescence spectroscopy. Furthermore, a novel UHV-compatible liquid-cell developed to investigate liquids and solidliquid interfaces will be presented. Protein attachment at the solid-liquid interface was investigated by detection of the characteristic N1s→π*(O=C-N) amide bond resonance in the N K-edge NEXAFS by using ultra-thin epoxy-functionalized SiC-windows.
Measuring the moisture state of screeds is critical for floorers in order to prevent structural damages of bottom coverings. Typically destructive tests are carried out on small samples delivering only punctual information. We tested several non-destructive testing methods in terms of sensitivity in the critical low moisture range and observed substantially different drying behavior for the two tested cement based and calcium-sulphate based screed samples. Our findings are supported by moisture gradient measurements using the nuclear magnetic resonance technique.
In recent years, elemental imaging of biological samples using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) is gaining in importance. Recent improvements regarding spatial resolution (down to 1 µm) and washout time make LA-ICP-MS particularly interesting for single cell analysis.
Many current nanomaterials can serve as contrast agents in cellular or tissue imaging, drug delivery vehicles or therapeutics, whereas others can cause toxic effects. In order to evaluate nano-bio interactions, the number of nanoparticles (NPs) inside cells as well as their localisation within cellular substructures is of particular interest.
LA-ICP-MS was used to study the NP pathway from uptake, via intracellular processing up to cell division. Fibroblast cells were incubated with different metallic NPs under varying experimental conditions. For LA analysis the cells were fixed with formaldehyde and dried.
Our results show that LA-ICP-MS is able to localise NP aggregates within cellular substructures. The NPs accumulate in the perinuclear region in the course of intracellular processing, e.g. multivesicular fusion and endosomal maturation, but do not enter the nucleus [1, 2]. A strong dependence of NP uptake on concentration and incubation time was found. Additionally, the number of NPs internalized by individual cells was determined and variations within the cell population became visible.
A new laser ablation system providing a short washout time (50 ms) together with small spot sizes (< 4 µm) and high repetition rates allows high spatial resolution applications. First results of cell imaging will be shown.
The findings demonstrate the potential of LA-ICP-MS providing insight into NP uptake and intracellular distribution dependent on experimental parameters.
Eight different screed types are tested including two different sample heights of 35 and 70 mm. The moisture of the four cement based and four sulphate based screeds are monitored during hydration and evaporation. All samples are stored in a climatic chamber at 23° C and 50 % relative humidity. Embedded sensors like temperature arrays, humidity sensor arrays, and multi-ring electrodes are embedded in the samples to yield a detailed moisture evolution with high depth resolution. Furthermore, nuclear magnetic resonance is used to quantify the water content at different depths. This multi-sensor approach allows a comprehensive monitoring of the moisture and its gradient in the different screed samples. This yields a deeper insight into the hydration, moisture convection, and diffusion processes.
Pollen represent one major cause for human allergic diseases. Currently the characterization and identification of pollen is time-consuming since it mainly relies on the microscopic determination of the genus-specific pollen morphology. A variety of new analytical approaches, like Raman - and fluorescence spectroscopy have been proposed in order to develop fast and reliable pollen identification. Recently matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) was initially applied for the rapid investigation of such complex biological samples. Taxonomic differences and relations of single pollen grains could be identified.
Both commercially available lyophilized pollen and fresh pollen acquired from biological samples collected in parks and in the Botanical Garden Berlin in the years 2013-2015 were investigated. The samples were prepared by formic acid extraction in the gas phase and spotted with HCCA matrix. A variety of new approaches, like a newly developed MALDI target with micrometer sample spots sizes, were tested for their suitability. The obtained mass spectral data were investigated by principal component analysis (PCA).
The applicability of MALDI-TOF mass spectrometry for the classification of pollen according to their taxonomic relationships was proven. Specifically, chemical differences in the mass spectra at the levels of plant order, genus and in many cases even of species could be identified. Based on these results, further investigations have been undertaken to optimize the sample preparation for the classification of single pollen grains in mixtures of pollens. A novel MALDI-target design was developed to enhance the phenotypic information of pollens in their mass spectra. The combination of mass spectral patterns and multivariate statistics provide a powerful tool for the investigation of structural correlations within mixtures. The results can be used to improve the reconstruction of taxonomic relations of single species in various mixtures and might be useful for the development of a fast routine method to identify pollen based on mass spectrometry.
To quantify the moisture in concrete, RFID based humidity sensors are embedded. Passive high frequency, ultra-high frequency RFID tags as well as active Bluetooth sensors are tested. After concreting, all sensors measure the corresponding relative humidity to monitor the concrete moisture. Two case studies are performed, embedding in an existing construction, i.e. the duraBASt test bridge, and embedding in cement based mortar in the laboratory. As basis for robust and long-life sensors in alkaline concrete, different casing materials are tested. Furthermore, signal strength measurements and their sensitivity to different moisture levels are performed.
Der Einsatz moderner Prozessanalysentechnik führt zu einer Datenflut, deren Verarbeitung und Nutzung häufig nicht ohne den Einsatz von Chemometrie zu realisieren ist. Dafür stehen zahlreiche multivariate Verfahren, wie z.B. Hauptkomponentenanalyse (PCA) und Regressionsanalyse (PLSR) für die Klassifizierung und für die quantitative Analyse zur Verfügung. Darüber hinaus können in Spezialfällen, insbesondere in der Spektroskopie, Methoden des „Indirect Hard Modeling“ eingesetzt werden. Anhand einer Industrie-relevanten Reaktion, der Hydroformylierungsreaktion zur Bildung langkettiger Aldehyde aus der Reaktion von Alkenen und Synthesegas, die sowohl im Labormaßstab als auch in einer Miniplant in Kooperation mit der TU Berlin untersucht wurde, werden Kalibrationsstrategien (Design of Experiment, DoE) und Auswertungsansätze mittels PLSR prozessbegleitender Raman Spektren dargelegt. Auf Grundlage des chemometrischen Ansatzes ist eine on-line Überwachung der Reaktion hinsichtlich der Hauptreaktanden, 1-Dodecene und 1-Tridecanal, möglich. Weiterhin konnte mittels Raman Spektroskopie die Bildung eines unerwünschten Nebenprodukts nachgewiesen werden.
The design of sample flow cells, commonly used in online analytics and especially for medium resolution NMR spectroscopy (MR-NMR) in low magnetic fields, was experimentally and theoretically investigated by 1H-NMR and numerical simulations. The flow pattern was characterised to gain information about the residence time distribution and mixing effects. Both 1H-NMR imaging and spectroscopy were used to determine the characteristics of flow cells and their significance for on-line measurements such as reaction monitoring or hyphenated separation spectroscopy. The volume flow rates investigated were in the range from 0.1 to 10 ml/min, typically applied in the above mentioned applications. When compared to those commonly used in high-field NMR, the special characteristics of flow cells for MR-NMR were revealed by various NMR experiments and compared with CFD simulations. The influence of the design of the inlet and outlet on the flow pattern was investigated as well as the effect of the length of the cell. For practical use, a numerical estimation of the inflow length was given. In addition, it was shown how experiments on the polarisation build-up revealed insight into the flow characteristics in MR-NMR.
Der Vortrag stellt die aktuellen Forschungsschwerpunkte zum Thema Prozessanalytik an der Bundesanstalt für Materialforschung und -prüfung (BAM) vor und nennt aktuelle Entwicklungsfelder mit dem Ziel gemeinsamer F&E-Projekte. Zunächst wird die Prozessindustrie und ihre Wertschöpfungskette vorgestellt. Daraus ergibt sich eine Motivation für Prozessanalytik. Zwischen der Prozessanalytik in der Pharmazeutische Industrie und der Chemischen Industrie bzw. Verfahrenstechnik gibt es Unterschiede, die herausgearbeitet werden. Der Vortrag schließt mit Technologiewünschen und Technologievisionen und nennt Konkrete Beispiele für Visionen für PAT, insbesondere im Kontext des Zukunftsprojekts „Industrie 4.0“
A comprehensive characterization of plasma modified polymer surfaces or plasma-polymerized thin films needs access to parameters as
- concentration of saturated/unsaturated carbon species (e.g. aromaticity) or other double bonds as C=N or C=O,
- branching, and
- losses of crystallinty or other degrees of structural order.
Furthermore the complex ageing phenomena of plasma modified polymers/plasma-polymers and the measurement of an in-depth distribution of chemical species are challenges for the analyst. The talk will display selected examples where such challenges have been met by using advanced methods of surface chemical analyses as Photoelectron Spectroscopy with variable excitation energy (“SyncXPS”), X-ray Absorption Spectroscopy (NEXAFS) at C, N and O K-edges and Time-of-Flight Secondary Mass Spectroscopy (ToF-SIMS) combined with Principal Component analysis (PCA).
Novel air-coupled ultrasonic transducer combining the thermoacoustic with the piezoelectric effect
(2016)
In recent years, there has been an increasing industrial demand for one-sided inspection of various structures by means of air-coupled ultrasonic technique. Lightweight structures based on carbon-fibre-reinforced polymers may have very complex shapes, making air-coupled transmission difficult or even impossible. The inspection of concrete structures is another example where one-sided inspection is required.
To address these challenges a new type of transducer for air-coupled pulse-echo inspection was developed, which unites two principles: thermoacoustic emission and piezoelectric reception. The thermoacoustic emitter is a titanium electrode with a thickness of several tens of nanometer. This electrode was deposited onto charged cellular polypropylene, which serves as a piezoelectric receiver. The thermoacoustic transmission is based on a transformation of the thermal energy of an electrically heated electrode into the acoustic energy of an ultrasonic wave. Thermoacoustic emitters provide resonance-free behaviour and thus extremely broadband pulses. Charged cellular polypropylene is piezoelectric due to the polarization of its cells and it is well matched to air, with a Young modulus in the order of magnitude of MPa. In this contribution we present some pulse-echo measurements with the first prototypes of the combined thermoacoustic-piezoelectric transducer.
A round robin test on flash thermography was organized within the scope of a standardization research project. This test gives information on reliability, comparability and efficiency of different testing situations. Data recorded on metal and CFRP test specimens with flat bottom holes (FBH) were analysed by evaluating the detectability and by calculating the signal-to-noise ratio (SNR) of the defect signatures as a function of defect parameters. For the investigation of the influence of material properties on the spatial resolution as well as on penetration depth, test specimens made of steel and copper with crossed notches and a notch ramp were constructed and investigated. Here, the minimum resolvable notch distance and the maximum detectable depth of the ramp were analysed.
A model is presented that employs a unified approach for
simulating the photon energy spectra for transmission and direct
beam targets composed of arbitrary homogeneous materials. In order
to achieve this, a detailed model of electron transport within the
target is employed. The validity of the developed model is shown
through comparisons with Monte Carlo simulations as well as
measurements for a number of different configurations.
Modelling becomes more and more important in modern NDE. It is increasingly used to optimize techniques for complex applications, to support the preparation of written procedures, and for education purposes. To describe the complete chain of RT, the model includes simulating all necessary properties of X- or Gamma-ray sources, the interaction of photons with material with special attention to scattered radiation, the detection process, and the complete geometrical RT setup handling arbitrary parts or constructions. Depending on the given inspection problem and the influencing factors that should be addressed by the simulation, an appropriate physical model has to be chosen to describe the underlying interaction mechanisms. The simulator aRTist combines analytical and Monte Carlo methods to efficiently model the radiation transport such that transmission as well as scatter techniques can be modelled. In this contribution we focus on Monte Carlo simulation of scatter contribution within aRTist. Examples for RT/tomographic applications and back-scatter techniques are presented to demonstrate the usability of the presented simulation tool for a broad range of radiological applications.
In this contribution, we discuss the influence of scattered radiation on materials’ effective attenuation coefficients at higher X-ray energies. The selected X-ray spectra for the dual-energy experiments correspond to 3 MV and 7.5 MV acceleration potential of the used betatron. Experiments were performed on a test phantom containing step wedges of different low- and high-Z materials. We evaluated the ratio between low- and high-energy X-ray attenuation coefficients quantitatively based on simulated poly-energetic high-energy X-ray source spectra and the detector sensitivity using the “analytical Radiographic Testing inspection simulation tool” (aRTist) developed at BAM. Furthermore, the influence of scattered radiation is evaluated using an efficient Monte-Carlo simulation. The simulation results are compared quantitatively with experimental investigations. Finally, important applications of the proposed technique in the context of aviation security are discussed.
X-ray backscatter imaging is a well established NDT technique to inspect complex objects using only a single-sided access. In difference to conventional transmission X-ray radiography, the X-ray backscatter imaging utilizes the scattered radiation caused by the Compton scattering effect. In order to achieve high backscatter intensities from a test object, it is necessary to optimize the backscatter system parameters namely the angle between source and slit camera, the slit collimator system, the shielding between source and scatter camera, and the type of detector. In addition, the scatter phenomena in to the investigated object need to be understood.
In this contribution, we present a Monte Carlo model McRay which considers all relevant single and multiple interactions of photons and electrons. This model can be used to simulate back scatter techniques. It allows not only calculating the scatter image for a given experimental setup but also registering the spectrum of the detected scattered photons. Both aspects are important to understand the imaging process, to interpret the results, and to optimize the backscatter camera investigated here. Additionally experimental results will be presented and compared with simulations.
Electromagnetic waves with frequencies between 0.1 and 10 THz are described as THz-radiation (T-ray). The ability to penetrate dielectric materials makes T-rays attractive to reveal discontinuities in polymer and ceramic materials. THz-Time Domain Spectroscopy Systems (THz-TDS) are available on the market today which operates with THz-pulses transmitted and received by optically pumped semiconductor antennas. In THz-TDS the travelling time (ToF) and shape of the pulse is changed if it interacts with the dielectric material and its inherent disconti-nuities. A tomogram of the object under the test can be reconstructed from time of flight diffraction (ToFD) scans if a synthetic focusing aperture (SAFT) algorithm is applied. Otherwise, planar discontinuities like cracks in plastics or delaminated lay-ers in composites can be abstracted as layers located at any angle in relation to the outer sample surface direction. A tomogram from the scanned sample can then be reconstructed in case the interactions of electromagnetic pulses with the existing in-herent interfaces are detectable and a model is assumed which describes the device under the test as multilayer structure composed of thin layers with different dielec-tric properties.
A short description of both the SAFT – and Optical Layer algorithm for the recon-struction of the inherent structure is initially given. Measurements on representative samples with a variety of artificially produced small and large scale. Reconstructed tomograms are presented to discuss and evaluate the benefits and limits of the two different reconstruction approaches.
For the last 20 years active thermography has developed into a standard method in non-destructive material testing. It has become possible to detect defects such as cracks, voids, or even material inhomogeneities. Until now, it is still difficult to quantify subsurface or hidden defects in size due to the diffusive nature of heat flow within a solid. Facing this issue, lockin thermography and other photothermal techniques have been established. They are based on exciting a sample periodically (e.g. with a halogen lamp), causing a controlled periodical heat flow and thereby representing strongly damped thermal waves. These techniques make use of interference and reflection of thermal waves which allow enhancing depth resolution.
So far, only the temporal component of the light source was modified to achieve a defined vertical heat flow – In contrast, we propose a novel technique in which we are able to control both: time and space. This technique enables us to exploit the possibilities of coherent thermal wave shaping. We achieve that by combining a spatial light modulator (SLM) with a high power laser. This approach allows us to launch a set of individually controlled and fully coherent high energy thermal waves into the sample volume. That means, we intentionally use wave propagation throughout the sample’s material in both - vertical and lateral direction.
As one possible application, we use a thermal waves’ interference effect of two phase shifted wave patterns to detect the position of hidden defects. The wave patterns are positioned with a certain distance and a 180° phase shift to each other creating an amplitude depletion zone right in the middle of the two patterns. When a defect is brought unsymmetrically into the depletion zone, the lateral heat flow is disturbed. If the sample is now moved through the depletion zone, a defect can be easily characterized. Exciting periodically while controlling simultaneously phase and amplitude enables us to have a defined thermal wave propagation throughout the sample which means thermal waves can be controlled almost like acoustical or optical waves. This offers the opportunity to transfer known technologies from wave shaping techniques to thermography methods.
Applications of fibre reinforced plastic (FRP) composites in modern industries are increasing due to their considerable advantages such as light weight and excellent mechanical properties. Accordingly, importance of operational safety of modern structures made of advanced composites by ensuring the material quality has led to increasing demands for development of non-destructive evaluation (NDE) systems. In the context of a European project entitled “Validated Inspection Techniques for Composites in Energy Applications” (VITCEA), the aim is to develop and validate traceable procedures for novel NDE techniques with contrasting damage detection capabilities in energy related applications such as wind and marine turbine blades, nacelles, oil and gas flexible risers. Accordingly, VITCEA focuses on optimization of ultrasonic tests (UTs) for quantitative defect detection and quality characterization of FRP structures. In this context, the present study describes the ultrasound field in heterogeneous composite materials. The theoretical predictions are compared with simulation results obtained from CIVA a software package dedicated to NDT simulations based on the asymptotic ray theory.
Der Vortrag beschäftigt sich mit den materialwissenschaftlichen Aspekten des Buchdrucks. Hierbei geht es weniger um die Darstellung und Erklärung der unterschiedlichen Druckverfahren (Hochdruck, Tiefdruck, Flachdruck und Durchdruck), diese werden nur am Rande gestreift, um die Vielfalt der unterschiedlichen Drucktechniken darzulegen. Vielmehr beschäftigt sich der Vortrag mit den Materialien, d.h. Druckfarben, die sich dann tatsächlich auf dem Schriftträger analysieren lassen. Unterschiedliche Drucktechniken (und Effekte) erfordern unterschiedliche Materialzusammensetzungen - diese werden innerhalb des Vortrags diskutiert.
Excelling in brevity but lacking in applicability, the 2011 EU nanomaterial definition has become a source of anguish for scientists and industry alike. Repeated pleas and discussions with our own envoy have demonstrated the strength of their resolve: this definition is unlikely to change. Manufacturers of many materials (cosmetics, pigments, foodstuffs, etc.) will have to characterise and label all their products accordingly, a task still impossible for lack of a clear metrological approach towards this goal. Therefore, the onus has fallen on the scientists to come up with a practicable measurement technique allowing inexpensive classification covering large swathes of the material landscape. Small-angle X-ray Scattering (SAXS) probes the size range in question, and can - with due care - deliver a bulk-averaged volume-weighted size distribution. Like any other real-world measurement method, however, it is not (and can never be) a universal solution. This presentation will clarify the SAXS technique, provide several application examples for nanomaterial characterisation, and will detail the limitations and pitfalls that accompany its abilities. At the end of this presentation, you will have the information to judge whether the technique is amenable to your materials or not.
In recent years, elemental imaging of biological samples using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) is gaining in importance. Latest improvements regarding spatial resolution (down to 1 µm) and washout time make LA-ICP-MS particularly interesting for single cell analysis.
Many current nanomaterials can serve as contrast agents in cellular or tissue imaging, drug delivery vehicles or therapeutics, whereas others can cause toxic effects. In order to evaluate nano-bio interactions, the number of nanoparticles (NPs) inside cells as well as their localisation within cellular substructures is of particular interest.
LA-ICP-MS was used to study the NP pathway from uptake, via intracellular processing up to cell division. Fibroblast cells were incubated with different metallic NPs under varying experimental conditions. For LA analysis the cells were fixed with formaldehyde and dried.
Our results show that LA-ICP-MS is able to localise NP aggregates within cellular substructures. The NPs accumulate in the perinuclear region in the course of intracellular processing, e.g. multivesicular fusion and endosomal maturation, but do not enter the nucleus [1, 2]. A strong dependence of NP uptake on concentration and incubation time was found. Additionally, the number of NPs internalized by individual cells was determined and variations within the cell population became visible.
A new laser ablation system providing a short washout time (50 ms) together with small spot sizes (< 4 µm) and high repetition rates allows high spatial resolution applications. First results of cell imaging will be shown.
The findings demonstrate the potential of LA-ICP-MS enabling insight into NP uptake and intracellular distribution dependent on experimental parameters.