Analytische Chemie
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Der Ersatz von Röntgenfilmen durch digitale Detektoren in der zerstörungsfreien Prüfung wurde in den letzten 10 Jahren kontrovers diskutiert. Nach der Erfolgsgeschichte der digitalen Photographie und der fast vollständigen Ablösung der Filmtechnik in der optischen Bilderfassung wurde erwartet, dass sich der Übergang von der Filmradiographie zur digitalen Radiographie schnell vollziehen sollte. Dieser Trend ist derzeit so noch nicht zu beobachten. Zur mobilen Prüfung wird in Europa immer noch vorrangig die Filmradiographie und nur teilweise die Speicherfolientechnik eingesetzt. Im Bereich der stationären Prüftechnik haben sich die Matrixdetektoren (DDA) weitgehend durchgesetzt, wobei es auch hier noch alternative Detektoren wie Bildverstärker und Fluoroskope gibt. Mit Einführung der DIN EN ISO 17636-2 wird seit 2013 erstmalig geregelt, wie man einen digitalen Detektor für die technische Radiographie auswählen soll, um im Vergleich zur Filmradiographie eine äquivalente Bildqualität zu erhalten. Essentielle Parameter bestimmen, ob die geforderte Bildgüte erreicht werden kann. Es wird ein Überblick gegeben, welche Parameter zum praktischen Einsatz wichtig sind und wie sie ermittelt werden. Erste Erfahrungen im praktischen Einsatz werden diskutiert.
X-ray backscatter imaging is a promising 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 the source and scatter camera, and the type of detector. Here a single-slit as well as a multi-slit camera are considered. For the multi-slit camera several twisted slits were parallel arranged in a metal block. This camera generates a set of similar projections per slit overlaying each other. Afterwards, the image is corrected based on a de-convolution algorithm to focus the overlaying projections into a single representation of the object.
The scatter phenomena in the object under inspection are investigated. In this contribution, the Monte Carlo model McRay is discussed, which considers all relevant single and multiple interactions of photons and electrons. This model can be used to simulate back scatter techniques. Simulations are important to describe the imaging process, to interpret the results, and to optimize the backscatter camera investigated here. Experimental results will be presented and compared with simulations.
Airborne ultrasonic inspection is performed in through transmission, where the test piece (e.g. adhesive joint or polymer-based composite plate) is placed between the transmitter and the receiver. However, many structures with difficult shapes allow only one-sided inspection. The strong reflection of the signal from the surface overshadows the signals from the inside, so that broadband pulses are required. Thermoacoustic transmission, where the thermal energy of an electrically heated electrode is transformed into the acoustic energy of an ultrasonic wave, opens the possibility to excite broadband pulses and thus to inspect objects with one-sided access.
We present various thermoacoustic transducers consisting of an electrically conductive film on a solid substrate. The first type of transducer is a transmitter with an indium-tin-oxide electrode on a glass substrate combined with a laser Doppler vibrometer as a receiver. The second type of transducer combines thermoacoustic transmission and piezoelectric reception, having a titanium electrode as a transmitter deposited onto charged cellular polypropylene serving as a piezoelectric receiver.
Using a focusing thermoacoustic transmitter and a separate cellular polypropylene receiver, a through-transmission inspection of a 4 mm thick CFRP test piece with inserts as small as 1 mm was performed. The same emitter and a laser vibrometer as a receiver were used for a one-sided inspection of a Plexiglas block with a cross hole at 15 mm depth. A twin probe consisting of a thermoacoustic transmitter on a cellular polypropylene receiver was applied to a profile measurement on a step wedge with flat bottom holes. The smallest detected diameter of a flat bottom hole was 1 mm. Sound pressure level above 140dB was achieved with each of these transmitters. Thermoacoustic transmitters enable a step towards one-sided air-coupled ultrasonic inspection.
Im Rahmen der Lebensdauerverlängerung oder der Umnutzung von Bauwerken (z. B. Brücken, Bürogebäude oder Maste) müssen diese zum Teil neu bewertet werden. Dafür ist eine Nachrechnung für statische und dynamische Lastfälle erforderlich. Dies betrifft zum einen die Struktur selbst, die gegebenenfalls verstärkt werden muss. Aber auch die Gründung (oft Pfähle verschiedenster Typen) muss neu beurteilt werden. Nach mehreren Jahrzehnten sind jedoch für einige Bauwerke keine zuverlässigen Bestandsunterlagen verfügbar.
Eine vollständige Freilegung der Pfähle verbietet sich aus Kostengründen sowie Verlust an Widerstand gegen Zug. Lediglich der Pfahlanschluss kann visuell begutachtet werden, um Pfahlzahl, -typ und Durchmesser zu bestimmen. Für die Bestimmung der Pfahllänge müssen zerstörungsfreie Verfahren eingesetzt werden. In einer Machbarkeitsstudie wurden von den Autoren teils im Blindversuch drei Verfahren evaluiert: die klassische Pfahlintegritätsprüfung nach der Hammerschlagmethode, eine mehrkanalige Variante hierzu und das Parallel-Seismik-Verfahren. Die ersten beiden Methoden lieferten an den untersuchten Pfählen nur in Einzelfällen verwertbare Ergebnisse. Die Parallel-Seismik-Methode lieferte auch im Blindversuch an Fundamenten, bei denen die Pfahllänge dem Eigentümer bekannt war, Ergebnisse mit einer Abweichung von max. 0,5 m. Diese Toleranz lässt sich bei der Standfestigkeitsbeurteilung berücksichtigen. Die Mehrkosten des Verfahrens (anders als bei den anderen Verfahren wird ein verrohrtes Bohrloch im Boden nahe dem Pfahl benötigt) halten sich in Grenzen, wenn man es in die geotechnische Untersuchung integriert. Daher wurde es inzwischen auch in der Praxis eingesetzt. Auch liegen die Gesamtkosten für die Untersuchung deutlich unter denen für eventuell notwendigen Ersatz – oder Verstärkungsmaßnahmen, die notwendig werden, wenn keine Daten zur Pfahllänge verfügbar sind.
Der Vortrag erläutert die Ergebnisse der Machbarkeitsstudie, zeigt erste Praxisfälle und weist auf Möglichkeiten hin, das Parallel-Seismik Verfahren in Zukunft noch genauer und effizienter einzusetzen.
Der Vortrag widmet sich der Kratzbeständigkeit-Prüfmethoden und deren Bewertung und beschreibt Begriffe/Definitionen, Wirtschaftliche Bedeutung der Kratzbeständigkeit, Mess- und Prüfverfahren – allgemein (Anwendbarkeit, Messunsicherheit, Validierung), Mess- und Prüfverfahren – speziell die Erzeugung, Prüfverfahren von Einzel- und Vielfach-Kratzern, die Charakterisierung von Verkratzungen und eine zusammenfassende Bewertung im Einzelnen
Durch das alkalische Porenwassermilieu ist Stahl im Beton vor Korrosion geschützt. Unter un-günstigen Umgebungsbedingungen (Karbonatisierung, Chlorideintrag) kann die passive Deck-schicht auf der Stahloberfläche zerstört werden. Im weiteren Verlauf können sich korrosionsbe-dingte Folgeschäden, wie Risse und Abplatzungen am Bauwerk ergeben. Um notwendige Sanie-rungsmaßnahmen sind frühzeitige und weitgehend zerstörungsfrei ermittelte Informationen über das aktuelle Korrosionsverhalten der Stahlbewehrung von großer Bedeutung. Die Potentialfeld-messung ist ein etabliertes und weit verbreitetes Verfahren zur Beurteilung des Korrosionszu-standes der Bewehrung in Stahlbetonbauwerken. Mit Hilfe dieses Verfahrens können Bereiche aktiv korrodierender Bewehrung zerstörungsfrei lokalisiert werden. In der Regel kommt diese Messmethode bei der Detektion chloridinduzierter Korrosion zum Einsatz.
Im Rahmen der Lebensdauerverlängerung oder der Umnutzung von Bauwerken (z. B. Brücken, Bürogebäude oder Maste) müssen diese zum Teil neu bewertet werden. Dafür ist eine Nachrechnung für statische und dynamische Lastfälle erforderlich. Dies betrifft zum einen die Struktur selbst, die gegebenenfalls verstärkt werden muss. Aber auch die Gründung (oft Pfähle verschiedenster Typen) muss neu beurteilt werden. Nach mehreren Jahrzehnten sind jedoch für einige Bauwerke keine zuverlässigen Bestandsunterlagen verfügbar.
Eine vollständige Freilegung der Pfähle verbietet sich aus Kostengründen sowie Verlust an Widerstand gegen Zug. Lediglich der Pfahlanschluss kann visuell begutachtet werden, um Pfahlzahl, -typ und Durchmesser zu bestimmen. Für die Bestimmung der Pfahllänge müssen zerstörungsfreie Verfahren eingesetzt werden. In einer Machbarkeitsstudie wurden von den Autoren teils im Blindversuch drei Verfahren evaluiert: die klassische Pfahlintegritätsprüfung nach der Hammerschlagmethode, eine mehrkanalige Variante hierzu und das Parallel-Seismik-Verfahren. Die ersten beiden Methoden lieferten an den untersuchten Pfählen nur in Einzelfällen verwertbare Ergebnisse. Die Parallel-Seismik-Methode lieferte auch im Blindversuch an Fundamenten, bei denen die Pfahllänge dem Eigentümer bekannt war, Ergebnisse mit einer Abweichung von max. 0,5 m. Diese Toleranz lässt sich bei der Standfestigkeitsbeurteilung berücksichtigen. Die Mehrkosten des Verfahrens (anders als bei den anderen Verfahren wird ein verrohrtes Bohrloch im Boden nahe dem Pfahl benötigt) halten sich in Grenzen, wenn man es in die geotechnische Untersuchung integriert. Daher wurde es inzwischen auch in der Praxis eingesetzt. Auch liegen die Gesamtkosten für die Untersuchung deutlich unter denen für eventuell notwendigen Ersatz – oder Verstärkungsmaßnahmen, die notwendig werden, wenn keine Daten zur Pfahllänge verfügbar sind.
Der Vortrag erläutert die Ergebnisse der Machbarkeitsstudie, zeigt erste Praxisfälle und weist auf Möglichkeiten hin, das Parallel-Seismik Verfahren in Zukunft noch genauer und effizienter einzusetzen.
Der Vortrag widmet sich dem „RITZ-TEST: EVALUIERUNG UND STAND DER NORMUNG“ und beschreibt die Komponenten, Ergebnis und Messgrößen, nicht registrierende Prüfgeräte, Evaluierung Ritz-Test (Makrobereich), den Atlas der Versagensformen, Geräte für den instrumentierten Ritz-Test und die Normung des Ritz-Tests (ASTM) zur Bewertung der Haftfestigkeit“ im Einzelnen.
The basics of broadband dielectric spectroscopy were introduced in detail. The analysis of the data was discussed. As application of broadband dielectric spectroscopy the alpha-relaxation (dynamic glass transition), the chain dynamics of polymers, and the behavior of a high performance polymer were illustrated.
Presentation on recent progress in ultrasinic testing and monitoring of concrete for massive structures. First, a new instrument (LAUS) for ultrasonic echo testing of thicknesses up to 5 m is shown. A new method to provide better images of the concrete interior, Reverse Mitem Migration (RTM)is presented. Second, the use of embedded ultrasonic transducers and data processing methods borrowed from seismology to detect subtle changes in concrete are documented.
Hexagonal beta-NaYF₄ doped with 20 % Yb and 2 % Er is an efficient upconversion (UC) phosphor for the conversion of 976 nm to 845 nm, 655 nm and 540 nm light. The emission behavior of this material is strongly influenced by the particle size, surface chemistry, and microenvironment. Especially the design of nm-sized UC particles for bioanalytical applications requires reliable spectroscopic tools for the characterization of the optical properties of these materials like the UC quantum yield (QYUC) in aqueous media. The UC emission originates from multiphotonic absorption processes, rendering the QYUC excitation power density (P) dependent. The P-dependent absolute measurement of QYUC in aqueous media with an excitation wavelength of 976 nm presents a considerable challenge due to the low absorption coefficients of the UC materials and the absorption of water at this wavelength.
Here, we present the P-dependent QYUC of 21 nm, 26 nm and 31 nm-sized NaYF₄ UC particles dispersed in cyclohexane and aqueous solutions, in view of bioanalytical applications. To gain a better insight of the photonic nature of the upconversion mechanism and the quenching processes involved, the luminescence decay behavior as well as the P-dependent red-to-green luminescence intensity ratios and slope factors of the different emission bands are studied in both solvents. These results present an important step to the rational design of brighter upconversion nanoparticles.
Der Vortrag widmet sich dem „Ringversuch zur Klassifizierung von Kohlenstoffschichten mittels Ellipsometrie“ und beschreibt die experimentellen Eckdaten, die Ellipsometrie als Messmethode am Beispiel DLC auf Stahl, Proben vs. n-k Ebene vs. Ergebnisse des Ringversuches, messtechnische Bewertung des Ringversuches und normative Bewertung des Ringversuches sowie Schlussfolgerungen.
Der Stand der Normung im Bereich der Oberflächentechnik wird zusammengefasst. Aktuelle Normungsvorhaben zur chemischen Oberflächenanalyse, Rastersondenmikroskopie, Nanotechnologie, Oberflächenmesstechnik im Mikro- und Nanobereich, für Anwendungen von Kohlenstoffschichten sowie von Mess- und Prüfverfahren für metallische und anorganische Überzüge werden vorgestellt. Ein Ringversuch zur Klassifizierung von Kohlenstoffschichten mittels Ellipsometrie wird diskutiert. Abschließend wird das DIN-Terminologie Portal erläutert.
Fast digital radiography was used to observe the crack development during single pass bead-on-plate gas tungsten arc welding with a minifocus X-ray source and a digital detector array with 75-micrometer pixel size. The sample material were 5 mm thick AlMgSi plates. An acquisition rate of 12 frames per second and an exposure time of 40 ms per frame were used for real-time observation of the hot crack propagation during welding. The basic spatial resolution of the images is about 80 µm. A 3D laminographic reconstruction of the acquired 2D radiographic images gives access to the volumetric extent of the cracks in the welded sample. The parallel use of a high-speed camera during welding allows the real-time inspection of surface cracks. The development of surface cracks was compared with the crack’s distribution in the sample volume and these results were correlated to the used welding parameters.
SETNanoMetro, a European Seventh Framework project, seeks to develop standard synthetic routes and metrological characterisation methods for the development and production of TiO₂ nanoparticles and nano-sized coatings with highly-defined, homogeneous and reproducible characteristics, including bulk structure, size, shape and surface structure. These materials are being tested for their potential in selected technological applications, including as coatings on bone-substituting prostheses. The objective of this study was to assess how variations in morphology and chemistry of nano-sized TiO₂ coatings affect their biocompatibility in vitro.
The physico-chemical characteristics of TiO2 coatings can greatly influence their final performance. In SETNanoMetro, different deposition procedures are being set for applying films of TiO2 NPs with defined and homogenous thickness on supports of interest for the applications studied in the project. The selected substrates are the following: (i) Silica glasses for photocatalytic measurements, (ii) Ti-alloys for orthopedic and/or dental prostheses, and for cell cultures, and (iii) Conductive glasses (e.g. Fluorine doped Tin Oxide, FTO) for dye-sensitized solar cells. From the different film deposition procedures studied within the project Self-assembly of TiO2 NPs in multiple layers was selected. For this, surface modification of the substrate and of TiO2 nanoparticles (NPs) with e.g. silane coupling agents is a prerequisite. First attempts to prepare the self-assembled coating on the functionalized glass substrates seem to indicate that the functionalized NPs adhere to the substrates, even if the final coatings were not homogenous and presented agglomerates. ToF-SIMS results support this outcome.
In order to use the layer-by-layer deposition technique for the formation of TiO2 films by controlled self-assembly of the TiO2 NPs, the proper complementary moieties for the functionalization of the NPs were chosen. A first set of NPs has been produced by reaction with (3-aminopropyl)phosphonic acid (APPA) in order to functionalize the surface with free amino-groups. Then, the complementary NP set can be obtained from an aliquot of the first one, through the conversion of free surface amino-groups to aldehydes by reaction with glutaraldehyde. A proper approach for the functionalization of two types of TiO2, commercial P25 (Evonik) and SETNanoMetro-sample labelled UT001, with APPA was developed. A second set of NPs consisting of three types of TiO2 NPs, P25 and SETNanoMetro NPs (TiO2 NPs with high specific surface area > 150 m2/g and TiO2 NPs with low size < 20 nm) was functionalized with (3-aminopropyl)triethoxysilane (APTS). As for the previous set of NPs, the complementary NP set was obtained through the conversion of free surface amino-groups to aldehydes by reaction with glutaraldehyde. EDX, AES and ToF-SIMS spectra were collected and analyzed to demonstrate the presence of the surface functionalization of the different types of TiO2 NPs.
Cold neutrons are predominantly scattered at hydrogen when penetrating hydrogen-charged samples, resulting in a high image contrast between hydrogen and e.g. iron. The used radiographic set-ups consist of a neutron source, state-of-the-art scintillator screens and digital cameras. This allows monitoring diffusive hydrogen fluxes two-dimensionally with 20s temporal resolution. Such hydrogen fluxes can be quantified by using standards with known hydrogen content and similar sample thickness.
Neutron tomography generates three-dimensional models of the hydrogen distribution in steel. Such models gain new insight for damage analysis by showing the hydrogen accumulations around cracks and by enabling the hydrogen gas pressure estimation inside cracks.
The capabilities and limitations, as well as perspectives of this method will be discussed and illustrated with help of selected examples.
Bright emitters with photoluminescence in the spectral region of 800 – 1600 nm are increasingly important as optical reporters for molecular imaging, sensing, and telecommunication and as active components in electrooptical and photovoltaic devices. Their rational design is directly linked to suitable methods for the characterization of their signal-relevant properties, especially their photoluminescence quantum yield. Aiming at the development of bright semiconductor nanocrystals with emission > 1000 nm, we designed a new NIR/IR integrating sphere setup for the wavelength region of 600 – 1600 nm. We assessed the performance of this setup by acquiring the corrected emission spectra and quantum yield of the organic dyes Itrybe, IR140, and IR26 and several infrared (IR)-emissive Cd1-xHgxTe and PbS semiconductor nanocrystals and comparing them to data obtained with two independently calibrated fluorescence instruments absolutely or relatively to previously evaluated reference dyes. Our results highlight special challenges of photoluminescence studies in the IR ranging from solvent absorption to the lack of spectral and intensity standards together with quantum dot-specific challenges like photobrightening and photodarkening and the size-dependent air stability and photostability of differently sized oleate-capped PbS colloids. These effects can be representative for lead chalcogenides. Moreover, we redetermined the quantum yield of IR26, the most frequently used IR reference dye, to 1.1×10-3 in 1,2-dichloroethane DCE with a thorough sample reabsorption and solvent absorption correction.
Mechanochemistry is increasingly used for synthesizing various materials including metal organic compounds and cocrystals. Although this synthesis approach offers a fast and pure synthesis in high yields, there is a lack in understanding the mechanisms of milling reactions. The necessary data can only be obtained in in situ experiments, which were only recently established for milling reactions. Herein, we present a novel setup enabling a combined in situ investigation of mechanochemical reactions using synchrotron XRD and Raman spectroscopy.
The specific combination allows to study milling processes comprehensively on the level of the molecular and crystalline structure and thus obtaining reliable data for mechanistic studies. Besides well-known MOFs like ZIF-8, the formation process of new metal phosphonates and model cocrystals could be studied in detail. The syntheses pathway of the different compounds could be revealed. The results prove that the presented method combination is applicable for a wide range of materials and will provide the necessary understanding to tune and optimize mechanochemically synthesized compounds.
Starting out from Flory`s most probable Distribution concept, correct and incorrect evaluations of SEC measurements are discussed. Using the correct mode, polyesters prepared by irreversible and reversible polycondensation methods were studied. Polyesters of α,ω−alkanediols and isophthalic acid or polyesters of diphenols and sebacic acid were prepared by three different irreversible polyconcensation methods. Formation of cyclic oligo and polyesters was monitored by MALDI-TOF mass spectrometry and dispersities were measured by SEC. The results are compared with the theories of Flory and Odian.
Eqilibrated polyesters were prepared by reversible polycondensation of ethyl 6-hydroxycaproate or by alcohol-initiated ring-opening polymerization of ε-caprolactone. Various catalysts were compared. The influence of dilution and of di- or multifunctional initiators was evaluated. Furthermore, equilibrated polylactides were prepared from L- or meso-lactide at 120, 160 and 180°C. A fast even-odd equilibration was discovered in addition to reversible cyclization and intermolecular transesterification. The influence of these different equilibration mechanisms on the dispersity was investigated. The preparative and theoretical consequences are discussed.
2PM FlySCAN: Innovative approach for wide field high resolution imaging of skin tissue volumes
(2016)
Two Photon Microscopy (2PM) is an innovative Technology for high resolution imaging of human skin in vivo and ex vivo. Up to now the method is limited by its interdependence between the field of view and the attainable resolution. The new FlySCAN Technology overcomes these boundaries and enable images sizes of many millimeters by resolutions in the submicrometer range revealing very specific information on clinically and biologically relevant tissue and cell structures. The advantages of the new approach are demonstrated by excellent in vivo and ex vivo tissue images.
Mechanische Eigenschaften von Materialien im Mikro- und Nanobereich werden heute mit der Instrumentierten Eindringprüfung bestimmt. Das Verfahren ist bereits umfangreich in der DIN EN ISO 14577 Teil 1-4 genormt. Im Ergebnis des EU EMRP Projekts Dynamic mechanical properties and long-term deformation behavior of viscous materials (MEPROVISC)“ wurden die zwei neuen Normprojekte für die Instrumentierte Eindringprüfung „Linear elastische dynamische Eindringprüfung“ und „Eindringkriechen und zeitabhängige Eigenschaften“ vorgeschlagen und mit deren Bearbeitung im ISO/TC 164/SC3 Hardness Testing begonnen.
Ausgehend von der Darstellung der wesentlichen Ergebnisse des Projekts MEPROVISC werden die Grundzüge der neuen Normen in Bezug auf Kalibrierung, Methodik, Auswertung und Bestimmung der Messunsicherheit erläutert. Weiterhin werden die Möglichkeiten der aktiven Mitarbeit an diesen Normprojekten aufgezeigt.
Purity statements of high purity materials serving as primary standards by GDMS.
Primary standards are materials known for their total purity and therefore appropriate to realise the link with the International System of Units (SI). The realisation and dissemination of primary standards is of fundamental importance for comparability of measurement results through traceability in all fields of chemical analysis.
To serve as a primary standard for element determination the total purity of a high purity material needs to be measured. In order to achieve a sufficiently small uncertainty (i.e. < 0.01%) this involves determining all possible impurity contributions and to subtract their sum from the ideal purity of 100%.
GD-MS has the potential to reduce the effort for purity determination, as a fast sensitive multi-element analysis without extensive sample preparation. Similar to other solid sampling techniques, glow discharge
requires calibration link the measured signal and the content of the impurities in the matrix.
The use of the concept Relative Sensitivity Factors (RSFs) provides good approximations especially for high purity materials. However, it only works with a wide uncertainty of the results.
The preparation of synthetic pressed powder samples by different modifications of liquid and powder doping used for the determination of both metallic and none-metallic impurities are described. Efficient determination of metallic impurities by GD-MS via differential and absolute measurements with a significantly reduced target uncertainty of 20 % for absolute measurements using liquid doped pressed powder calibration could be achieved. The determination of impurities has been evaluated by independent analytical methods such as HR-ICP-MS, ETAAS; CGHE and combustion analysis
The presentation will give an overview on non-destructive testing techniques being developed at the Federal Institute for Materials Research and Testing, Germany (BAM). This includes ultrasonic methods, ground penetration radar, Laser-Induced Breakdown Spectroscopy (LIBS), infrared thermography, pile testing, sensor technology and building scanner. A focus of the talk will be ultrasonic methods, which are well established in various aspects of concrete testing. They are used for imaging the interior geometry of constructions, estimation of concrete strength or monitoring lab investigations. However, so far the detection of distributed damages, especially in an early stage, has been almost impossible. The arrival of new technologies as embedded transducers and sensitive data processing techniques adopted from seismology has opened new field of work. Recent research has been focused to detect changes in concrete elements induced by stress, temperature, moisture or chemical attacks by permanent monitoring. Techniques as Coda Wave Interferometry can resolve changes in ultrasonic velocity in the order of 1*10-5. In addition, many researchers believe that the investigation of nonlinear effects can be used to characterize damages. The presentation will give a wrap up of ultrasonic techniques currently used in practice. This will include echo based methods as multi-channel/multi-offset imaging of structural elements using commercial and prototype devices. Imaging methods as SAFT and RTM will be shortly discussed. The focus will be on the emerging techniques used for monitoring. New types of sensors will be presented as well as the devices used in laboratory and field applications. Insight will be given on the various influence factors on ultrasonic signals and various ways of feature extraction and data processing. The results of lab experiments will be shown to demonstrate the detection of various kind of damages from mechanical load, ASR, corrosion to fatigue. The experiences with our first installations in real constructions (bridges, tunnel) will also be presented.
Under the assumption of local thermal equilibrium, a numerical algorithm is proposed to find the equation of state for laser-induced plasmas (LIPs) in which chemical reactions are permitted in addition to ionization processes. The Coulomb interaction in plasma is accounted for by the Debye–Hückel method. The algorithm is used to calculate the equation of state for LIPs containing carbon, silicon, calcium, chlorine, nitrogen, and argon. The equilibrium reaction constants are calculated using the latest experimental and ab initio data of spectroscopic constants for the molecules N2, C2, Si2, CN, Cl2, SiN, SiC, CaCl, CaCl2 and their positive and (if existed) negative ions. The algorithm is incorporated into a fluid dynamic numerical model based on the Navier–Stokes equations describing an expansion of LIP plumes into an ambient gas. The dynamics of LIP plumes obtained by the ablation of SiC, CaCl2, solid silicon, or solid carbon in an ambient gas containing N2 and Ar is simulated to study formation of molecules and molecular ions. A particular attention is paid to formation of anions Cl−, Cl2−, Si2−, C2−, CN−, and SiN− in LIPs.
Integrating fluorescent probes with sensing matrices presents a major challenge because usually, when confined in a rather rigid matrix, fluorophores tend to behave completely different than for instance in the molecular state in solution. The lecture reviews the major strategies that have been devised recently to circumvent such issues with special focus on the works carried out in this field by BAM’s Chemical and Optical Sensing Division. Moreover, it will be shown that by using certain strategies not only can the response behavior be retained but synergistic effects can even endow the hybrid with a much better performance than the probe molecule alone.
Macrocycle-containing fluorescent probes continue to be one of the most popular classes of indicator molecules for the sensitive optical detection of ionic inorganic analytes, in particular metal ions, since the first integration of crown ether building blocks into chromophoric π systems more than 30 years ago. However, whereas a large multitude of such probes have been described for operation in organic or mixed aqueous environments, the step to realistic analytical media such as water samples, aqueous food extracts or body fluids is still scarce. On one hand, this is due to considerably low complex stability constants for instance for alkali and alkaline-earth metal ions. On the other hand, many classes of organic dyes that show favourable spectroscopic properties and ion-induced responses in organic solvents are not soluble in neat aqueous media and/or exhibit only significantly quenched fluorescence, even if transition metal ions are binding strongly to the receptor unit. A way to circumvent such problems in a rather simple manner is the steric incorporation of fluorescent probes into mesoporous silica nanomaterials. The local polarity in such pores, whether nascent or modified appropriately with functional silanes, resembles much more a quasi-organic environment while at the same time allowing for free diffusion of water and its cargo.
Two examples of powerful hybrid signalling systems will be presented, utilizing charge transfer-type indicator molecules that show inferior sensing properties in their molecular state. One example discusses mercury(II) determination over an extended concentration range and the other discusses silver(I) and mercury(II) discrimination simply on the basis of photophysical effects retained in the hybrid materials.
Since more than 20 years, optical spectroscopic techniques, in particular fluorescence-based methods, are on the rise in many different areas of chemical and biochemical analysis, with no end being in sight.1,2 Advances in miniaturization and remote applications on one hand and ground-breaking developments in microscopy and laser-based high-throughput instrumentation on the other hand have fuelled these developments substantially.3,4 At the core of utmost of these applications however is not only the instrument, but a small entity that is able to absorb and emit photons and thus to report on the actual (bio)chemistry that is going on in a particular sample of interest.5,6 Besides intense research on various types of luminescent particles (e.g., quantum dots and carbon dots) and proteins, dye chemistry has thus seen its revival and the number of publications dealing with the design, synthesis and application of new fluorescent dyes as probes, stains, labels or indicators is still continuing to grow.
Among the various classes of dyes available as bright fluorophores for a wavelength range that is compatible with many (bio)analytical applications and the respective instrumentation, in particular pyrrolic dyes that do not belong to the classical porphyrins or phthalocyanines have received strong attention recently. Starting perhaps with the revival of the traditional boron-dipyrromethene laser dye ca. 15 years ago,7 these so-called BODIPYs have developed into a colourful spectrum of different derivatives.8 However, the interest in expanding the range of pyrrole-containing π-systems beyond BODIPYs has also constantly increased and has brought about several other pyrrole-based ring systems such as diketopyrrolopyrroles9 or dipyrrolonaphthyridinediones which possess a favourable brightness and other interesting properties. The present contribution will give a critical overview of the field, pinpointing advantages and prospects as well as discussing potential aspects of improvement with an emphasis on the chemical sensing and the longer wavelength range.
Multiplexed bead-based array formats play an increasingly important role in analytical laboratories. Due to the high surface-to-volume ratio, fast reaction kinetics and modular assay design, these sensor formats are applied in clinical diagnostic, drug development and classical biosensors with great success.
As the spherical platform, researchers utilize micron sized particles made from polymeric or silica material. Such beads are commercially available from vendors such as BD or Luminex. However, we have encountered several problematic issues which accompany these platforms: first, bigger sized beads, which are required for particle handling reasons, are difficult to prepare with high monodispersity - a key requirement for cytometric application. Second, plain beads, made from either polymer or silica, have each several disadvantages such as inferior scattering properties in case of silica or limited flexibility for coupling strategies in the case of latex beads.
In order to overcome this problem, we have developed a versatile core-shell (CS) platform which consists of a polymeric core with a structurally controlled silica shell. In our approach, the core building block can be easily prepared with high yields and high monodispersity in a dispersion polymerization from approximately 500 nm to 1.3 µm. Then, silica is coated in a classical sol-gel process to protect the core with a stable yet modifiable surface (see SEM image in Figure 1, platform). Here, we combine ideal scattering properties and easy preparation of the polymeric core with the chemical flexibility of a silica surface. Moreover, the additional shell domain adds density to the composite, which makes particle handling feasible also for nanometer sized beads.
In this contribution we present proof-of-principle results of competitive immunoassays with fluorescence detection using our CS beads – each performed in mix-and-read fashion without washing steps. All sizes are applicable in cytometric read-out which and can be used for size encoding (see Set 1 to 3 in Figure 1, size encoding). However, further multiplexing for a set of at least 20 parameters can be achieved by swelling hydrophobic dyes into the core. To the same time, precise tuning of the surface with mixed silane layers allowed us to improve the selectivity towards small molecules in competitive immunoassays significantly (see example in Figure 1, Application). We believe that our platform allows researchers to gain access to superior assay performance in combination with a low-threshold approach for the synthesis of the spherical platform.
Gold ist eines der sieben schon im Altertum bekannten Metalle und wurde wg. seines Glanzes und seiner Seltenheit von alters her als Tauschmittel und zur Herstellung von Schmuck benutzt. Außerdem ist es einfach bearbeitbar und weitestgehend gegen chemische Einflüsse resistent.
Die Untersuchungen von Gold mit synchrotronstrahlungsangeregter Röntgenfluoreszenzanalyse sind zerstörungsfrei und geben Auskunft über die in der untersuchten Probe vorhandenen chemischen Elemente.
Bei den hier vorgestellten Untersuchungen an der BAMline stehen Fragestellungen wie Herkunft, Herstellungsverfahren und Zusammengehörigkeit von Goldfunden im Vordergrund. Die verschiedenen Fragestellungen werden an einer Reihe von Beispielen erläutert die vom Wikingerschatz aus Hiddensee über die Himmelsscheibe von Nebra bis hin zu Funden aus Ägypten langen. Zusätzlich werden die modernen Messmethoden vorgestellt, die am Synchrotron heutzutage zur Verfügung stehen.
Gold ist eines der sieben schon im Altertum bekannten Metalle und wurde wg. seines Glanzes und seiner Seltenheit von alters her als Tauschmittel und zur Herstellung von Schmuck benutzt. Außerdem ist es einfach bearbeitbar und weitestgehend gegen chemische Einflüsse resistent.
Die Untersuchungen von Gold mit synchrotronstrahlungsangeregter Röntgenfluoreszenzanalyse sind zerstörungsfrei und geben Auskunft über die in der untersuchten Probe vorhandenen chemischen Elemente.
Bei den hier vorgestellten Untersuchungen an der BAMline stehen Fragestellungen wie Herkunft, Herstellungsverfahren und Zusammengehörigkeit von Goldfunden im Vordergrund. Die verschiedenen Fragestellungen werden an einer Reihe von Beispielen erläutert die vom Wikingerschatz aus Hiddensee über die Himmelsscheibe von Nebra bis hin zu Funden aus Ägypten langen. Zusätzlich werden die modernen Messmethoden vorgestellt, die am Synchrotron heutzutage zur Verfügung stehen.
The Color X-ray Camera CXC or SLcam® is an energy-resolving X-ray camera capable of energy- and space-resolved measurements. It consists of a high-speed CCD detector coupled to a polycapil-lary optic that conducts the X-ray photons from the probe to distinct pixels onto the detector.
The camera is capable of fast acquisition of spatially and energy resolved fluorescence images. A dedicated software enables the acquisition and the online processing of the spectral data for all 69696 pixels, leading to a real-time visualization of the elements distribution in a sample. It was developed in a joint project with BAM, IFG Berlin and PN Sensors.
In this contribution we will mainly discuss the use of the CXC at our beamline, the BAMline at BESSY II and imaging applications of the CXC from different areas, like biology and archaeometry. Additionally new developments for the use of the detector without optics, like wavelength dispersive detection or 1shot-XANES, will be presented.
Im Nachlass Adelbert Chamissos, der in der Staatsbibliothek zu Berlin aufbewahrt wird, finden sich einige Zeichnungen – Lineamente – deren Inhalt rätselhaft ist. So ist nicht klar, was diese Zeichnungen darstellen und in welchem Zusammenhang sie entstanden sind. Die wenigen Aufschriften lassen weder eine eindeutige Identifizierung noch Datierung zu. Erste naturwissenschaftliche Untersuchungen widmen sich der Entstehungsgeschichte dieser Zeichnungen, der verwendeten Materialien und dem Auffinden möglicher Referenzen, um die Objekte in das Werk Chamissos einzuordnen.
Tattooing practice is adopted worldwide and represents a socio-cultural phenomenon, but the injection into the skin of coloring agents, such as metals might pose a serious health problem. Tattoo ink compounds are in general not officially controlled. Moreover, the origins as well as the chemical and toxicological specifications of these coloring agents are hardly known by the producers, the tattooists and by the consumers. In this view, the aim of this study was to characterize the metal composition of tattoo inks available in the market and to draw attention to the associated risk for human health.
A set of tattoo inks from the brand Kuro Sumi was analyzed by means of Synchrotron-based X-ray Fluorescence spectrometry (Sy-XRF) at BAMline @ BESSY II and Raman Spectroscopy using the XploRA confocal Raman microscope (785 nm laser) at the LIBPhys-UNL. Carbon black, rutile, phtalo blue, phtalo green, helizarin red, helizarin yellow and dioxazine violet were respectively identified in black, white, blue, green, red, yellow and violet inks. However, a wide range of transition and heavy metals, potentially hazardous was revealed by Sy-XRF. A semi-quantitative evaluation has revealed, in some inks, amounts of Cr, Cu, Zn and Pb higher than the allowed according to the resolution adopted by the Council of Europe on the safety of tattoos and permanent make-up.
Gold mosaics, made from gold and glass, are one of the best expressions of Late Antique Byzantine and Early Islamic art. The gold alloys, whose composition seems to indicate that gold coins were re-used to fabricate the tesserae, can be used to provide information on the mosaics chronology. Monetary Byzantine gold is in fact characterized by the presence of Pt, which contents in the gold alloy change over time, but Pt must be measured in 0.2-0.4 µm thickness gold leaves that were beaten to be sandwiched between two glass layers.
To analyze this samples the D²XRF set-up at the BAMline at the BESSY synchrotron in Berlin was used. The combination of a crystal for wavelength dispersion and an energy resolving single photon counting pnCCD allows the realization of this very simple wavelength dispersive detection system. With this system an MDL of 1 μg/g for the determination of Pt in Au under optimal conditions can be reached.
Gold leaf tesserae from nine archaeological sites, covering the period that goes from the 5th c. to the 8th c., were analyzed. The presence of Pt in the majority of the samples confirmed the re-use of coins. The Pt contents separate the samples in three groups, one of which having the same chemical characteristics as the Byzantine gold could be compared to dated coins for chronology. The higher Pt contents for one of other groups suggest
Die Mitte des 16. Jahrhunderts gegründete Dresdener Goldschmiedeinnung, geriet im 19. Jahrhundert in wirtschaftliche Schwierigkeiten, was letztendlich zu ihrer Auflösung führte. Im Zuge dessen wurde 1872 auch der historische Innungspokal für 80 Taler an das Grüne Gewölbe in Dresden verkauft. Sowohl das Empfehlungsschreiben des damaligen Direktors als auch die Zustimmung zum zügigen Ankauf dürften Beleg dafür sein, dass man damals der festen Überzeugung war, ein etwa 250 Jahre altes, authentisches Silbergefäß erworben zu haben. Die aktuelle kunstwissenschaftliche Begutachtung des Innungspokals lässt begründete Fragen zum Alter und zur Originalität des Objektes, welches heute in der Sammlung des Grünen Gewölbes präsentiert wird, aufkommen. Die kunst-wissenschaftliche und kunsttechnologische Expertise reicht hier allein ftir eine gesicherte Altersbestimmung nicht aus und soll deshalb durch naturwissenschaftliche Untersuchungen zur Materialzusammensetzung unterstützt werden.
Wilson´s disease, a rare genetic disorder of the copper metabolism, causes the copper accumulation in various organs, leading to manifold hepatic, neurological and psychiatric symptoms. To study the elemental distribution, human Wilson´s disease liver samples were analyzed by means of LA-ICP-MS. Results demonstrated an inhomogeneous copper and iron distribution in human liver with hotspots of very high intensities. Both elements were quantified by an external calibration using matrix-matched standards made of gelatin, showing concentrations up to several thousand micrograms per gram. Additionally, results were validated by means of synchrotron radiation based μXRF at the BAMline at BESSYII (Helmholtz-Zentrum Berlin).
Wilson´s disease (WD) is a rare genetic disorder of the copper metabolism, causing the accumulation of copper in different organs, including the liver, the central nervous system and cornea. This way, WD initiates manifold hepatic, neurological or psychiatric symptoms. To learn about the elemental distribution and present species in WD, liver samples were analyzed by laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS), micro X-ray fluorescence (μXRF) and X-ray absorption near edge structure spectroscopy (XANES).
Within this work, LA-ICP-MS was applied to study the distribution of copper and iron in human liver samples, which were collected by a liver biopsy of WD and control patients within a medical investigation. The analysis by LA-ICP-MS was performed with a 213 nm Nd:YAG laser using a spatial resolution of 10 μm and a scan rate of 20 μm/s. In a next step, copper and iron were quantified by LA-ICP-MS using homemade matrix-matched standards made of gelatin. Results showed an inhomogeneous copper and iron distribution in human liver with hotspots up to several thousand micrograms per gram liver within the hepatocytes.
Additionally, results for the elemental distribution in WD were validated by means of synchrotron radiation-based μXRF with a beam size of 4 μm at the BAMline at BESSYII (Helmholtz-Zentrum Berlin). Furthermore, XANES was performed to identify the present oxidation states of copper in WD, indicating a mixture of copper(I) and copper(II) within the liver tissue.
In the contemporary medicine, rhodanine staining is routinely used to determine the copper distribution in liver tissues. Nevertheless, this method does not provide results with a high sensitivity in comparison to LA-ICP-MS. Therefore, the presented LA-ICP-MS method offers a new possible diagnostic tool. These results may also contribute to a better understanding of Wilson´s disease and its development.
Core capability tables list the skills and experiences, which at least partially are needed to successfully carry out a specific analytical task within the IAWG. The required skills and experiences, so-called core capabilities (CC), are identified for each analytical procedure. The summarized CC tables are listed in the appendix of each report on the corresponding key comparison or pilot study. These CC tables enable us to demonstrate that we have the analytical procedure we claim under control by means of other Key Comparison, which do not exactly meet the claimed calibration and measurement capability. This is especially important for: a) fields where no Key Comparison is available, b) Revision of CMC claims or c) when a participation in a Key Comparison was not possible.
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.
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.
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.
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.
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.
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.
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.
Der Vortrag widmet sich Haftung und Haftfestigkeit bezüglich Grundlagen, Einflussgrößen sowie Prüfverfahren und beschreibt die Punkte: Generische und spezifische Motivation, Einflussgrößen auf Haftfestigkeit und Haftung von Beschichtungen, Prüfverfahren zur quantitativen Bestimmung der Haftfestigkeit und zur qualitativen Klassifizierung bzw. semi-quantitativen Bewertung der Haftung im Einzelnen.
Production of inorganic RM
(2016)
Beschrieben wird anhand von Beispielen die Vorgehensweise der BAM bei der Zertifizierung von Referenzmaterialien
Durch den Einsatz von eingebetteten faseroptischen Sensoren können Bauteile überwacht und frühzeitig Informationen über Materialveränderungen gewonnen werden. Um die Zuverlässigkeit eines solchen Sensors gewährleisten zu können, ist es wichtig, die korrekte Funktion des Sensors im Verbund mit einer Werkstoff-Matrix on-line und in-situ überwachen zu können. Im Rahmen des DFG-Projekts FAMOS² (FAser-basierter Magneto-Optischer SchichtSensor) wurde ein selbstdiagnose-fähiger Schichtsensor entwickelt, welcher mit Hilfe einer magnetostriktiven Aktorschicht validiert werden kann. Durch eine Kombination aus PVD (physical vapour deposition) und ECD (electro-chemical deposition) wird die Aktorschicht auf faseroptischen Sensoren haftfest abgeschieden. Ein äußeres Magnetfeldes dehnt die Aktorschicht und damit auch die Faser reversibel. Diese Dehnung führt zu einer Verschiebung der Bragg-Wellenlänge, welche direkt mit der Stärke des zu messenden Magnetfeldes korreliert. Ein etwa 100 Nanometer dünnes PVD-Schichtsystem aus Chrom und Kupfer dient zunächst als Haftvermittler zwischen Glasfaser und ECD-Schicht. Um eine rotationssymmetrische Schichtabscheidung zu erhalten, erfolgt während der PVD-Beschichtung eine Rotation der Faser. In einem klassischen Watts-Elektrolyten wird dann im zweiten Schritt die eigentliche etwa 30 Mikrometer dicke ECD-Aktorschicht auf die PVD-Schicht abgeschieden. Reine Ni-Schichten werden mit NiFe-Legierungen verglichen.
Die Geometrie der Faser stellt für die Herstellung und Charakterisierung der Schichten auf der einen Seite eine besondere Herausforderung dar, bietet aber zugleich auch neue experimentelle Möglichkeiten. So kann ggf. die Entstehung von Spannungen in der Schicht während der ECD-Abscheidung in-situ verfolgt werden, indem die Wellenlängenverschiebung aufgrund der Dehnung des Bragg-Gitters optisch gemessen wird. Die Anpassung der Beschichtungsverfahren an die Fasergeometrie sowie die Charakterisierung und die Eigenschaften der ECD-Schicht werden diskutiert. Insbesondere wird auf den Elastizitätsmodul der Aktorschicht eingegangen, wobei Werte aus der Nanoindentation und dem 2-Punkt-Biegeversuch mit der beschichteten Faser als Biegebalken verglichen werden.
Within the scope of a DIN INS project, a flash thermography round robin test that evaluates reliability, comparability, and efficiency of different testing situations was organized. The results give information about the detectability of defects, e.g. depending on their size and depth, the evaluation methods and the materials used. Besides, the influences of equipment and parameters used by the participants on the results were analysed. All of the quantitative results as well as the feedback given by the participants will be presented in a DIN committee in order to contribute to a flash thermography standard.
The duraBASt area at the highway intersection “Köln-Ost” is a large test field for road testing. It includes the duraBASt test bridge which is ca. 66 m long and 14.25m broad. This bridge is part of the “road in the 21st century” project and is equipped with several sensors for structural health monitoring. This feasibility study is realised to construct intelligent bridges in the future. Quantities like temperature, strain, moisture, corrosion, etc. are measured by embedded sensors. In the presented work, the focus lays on passive RFID-based sensors. The communication and energy supply is realised by a mobile transmitter through the concrete cover. Hence, no cables or batteries are required. The sensors are design to withstand in the alkaline environment in concrete. Thus, moisture and corrosion are detectable for several decades.
In civil engineering the information about the quantitative ingress of harmful species like Cl⁻, Na⁺ and SO²⁻₄ is of great interest to evaluate the remaining life time of structures. These species are triggering different damage processes like the alkali-silica reaction (ASR) or the chloride-induced corrosion of the reinforcement. For the evaluation of the heterogeneous concrete it is necessary to discriminate between the different phases mainly cement matrix and aggregates. The transport processes are only proceeding in the cement matrix therefore the measured concentrations should be regarded to the cement content. For the 2D evaluation of element distributions different multivariate cluster-algorithms like k-means and Expectation-Maximization-algorithm (EM-algorithm) have been tested. The methods are compared and different figures of merit will be presented. After phase separation non-relevant information of the aggregates can be excluded. The ingress of harmful species is then quantified using chemometrics. Due to concrete cores from a parking deck the methods have been validated and verified with standard methods of wet-chemistry.
Fluorophore labeled proteins and antibodies, referred to also as targeted optical probes, present a promising strategy for a variety of applications from fundamental cell-based biological studies to in vivo diagnostics and image guided surgeries in humans. In this respect, design strategies for the preparation of such conjugates from different dyes including analyte-responsive fluorophores are presented as well as their analytical and spectroscopic characterization employing Absorption spectroscopy and steady state and time-resolved fluorometry. Special emphasis is dedicated to the influence of dye hydrophilicity and labeling density on the optical properties and binding behavior of these dye-bioconjugates including their performance in in vitro and in vivo bioimaging studies.
Der Vortrag widmet sich der „Quantifizierung der Festigkeit von Kunststoffklebungen & -beschichtungen: Vorbehandeln, Kleben und Prüfen im OKTETT“ und beschreibt das Mehr-Proben-Konzept zur Herstellung und Prüfung von Klebeverbunden. Vorgestellt werden die Mehr-Proben-Klebevorrichtung sowie die Centrifugal Adhesion Testing (CAT) Technologie zur Bestimmung der Haft- und Klebefestigkeit von Beschichtungen (Al auf PP, SiO2 auf CR39).
The TiO2 material selected for the present inter-laboratory comparison (ILC) was the bipyramidal anatase UT001 batch synthesized hydrothermally by University of Turin in the frame of the EU/FP7 Project SETNanoMetro and carefully prepared on TEM grids by BAM to be distributed to the ILC participants. A clear measurement protocol including data analysis and reporting (including an xls reporting template) has been also prepared by BAM. 14 of 18 participants have measured and reported results which have been already checked by BAM as being conform to the agreed protocol. After receiving the last results (of 4 participants) the ILC data evaluation will be carried out by BAM in line with agreed ISO/TC229 procedures as for the other case sudies.
Entwicklung von Analysenverfahren, Standards und Referenzmaterialien für die Lebensmittelanalytik
(2016)
Mykotoxine gehören weltweit zu den am meisten untersuchten Kontaminanten in Lebensmitteln. Ihre zuverlässige Bestimmung ist zur Kontrolle geltender Grenzwerte notwendig und erfordert die Verfügbarkeit reiner Kalibrierstandards, valider Analysenverfahren sowie (zertifizierter) Referenzmaterialien. Im Vortrag werden die aktuellen Aktivitäten der BAM hinsichtlich der Entwicklung von Standards, Analysenverfahren und Referenzmaterialien für die Mykotoxin-Analytik vorgestellt.
Etwa 25% aller weltweit produzierten Nahrungsmittel sind mit Schimmelpilzgiften (Mykotoxinen) kontaminiert. Dies birgt nicht nur gesundheitliche Risiken sondern verursacht auch hohe wirtschaftliche Verluste. Daher werden in der EU seit Jahren Anstrengungen unternommen, die Mykotoxin-Analytik voranzutreiben und Grenzwerte zu etablieren. Im Vortrag werden aktuelle Trends der Mykotoxin-Analytik und entsprechende Bedarfe präsentiert. Neben einer verbesserten Verfügbarkeit rückführbarer nativer und isotopenmarkierter Standards treten verstärkt maskierte Mykotoxine in den Fokus.
In order to ground the debate on the metrics that apply for VSSA determined by adsorption isotherms and to illustrate the consequences of real bimodality for VSSA screening, a bimodal mixture has been selected for systematic investigations. A sample of BaSO4 fine was spiked with 10% g/g of BaSO4 ultrafine. The ultrafine grade is a clear nanomaterial (NM) according to the size criterion with a median Feretmin of 27 nm and the fine grade is clearly a non-NM with a median Feretmin of 249 nm. Because of the number ratio of 300:1, the mixture has to be a NM according to the size criterion. Three independent BET measurements were performed on the mixture by two different labs and resulted in a mean VSSA of 23 m2/cm3 with a standard deviation of 3.3 m2/cm3, which leads to a dminVSSA of 258 nm, and, therefore, would falsely classify the material as a non-NM. This effect was predicted earlier by calculated examples (Roebben et al. 2014) and demonstrates that mixtures of nano- and non-nano multimodal materials very likely lead to false negative classifications. Moreover, the measured VSSA values for the mixture of 23 m²/cm³ are in excellent accord with the value of 24.6 m²/cm³ predicted from the TEM size distributions of the individual materials according to the model described by JRC (Roebben et al. 2014), but are significantly different from the prediction of 309 m²/cm³ obtained from the same TEM size distribution by a particle number weighted approach (Lecloux 2015). The same is true for a 50% g/g mixture. We conclude that the mass-based VSSA approach (Roebben et al. 2014) is equal to the VSSA that is measurable by adsorption isotherms, such as from standardized BET.
A proposal of an inter-laboratory study (ILC) on determination of size and shape distribution of TiO2 nanoparticles (NPs) by transmission electron microscopy is presented. The anatase NPs synthesized in a controllable fashion within the EU/FP7 project SETNanoMetro can be considered as shape-defined (bipyramidal) and are offered to complete the list of case studies already in progress within ISO/TC229/JWG2. The main points of the measurement procedure are presented as well as a proposed procedure to evaluate the size and shape according to the standard operation procedure already developed within SETNanoMetro is discussed. Potential ILC participants and a plan with next step to be carried out are proposed.
High Speed X-ray Imaging and Spectroscopy with pnCCDs: XRF, XRD and PIXE measurements (and others)
(2016)
For many years pnCCDs have been well known as X-ray detectors for spectroscopic imaging in
many fields of science: X-Ray Fluorescence analysis (XRF), X-ray Diffraction (XRD) with light
sources in large accelerator facilities as well as with laboratory light sources or with X-rays from
celestial sources in X-ray astronomy. A brief introduction in GEXRF (Grazing Emission XRF)
measurements with a laboratory laser produced plasma source will be given, PIXE (Particle Induced
X-ray Emission) measurements and D2XRF (Double Dispersive X-Ray Fluorescence) and Slicing
experiments with pnCCDs coupled to polycapillary optics performed at the BESSY synchrotron will
be shown. Energy-dispersive Laue diffraction with ultra-hard X-rays for the analysis of defects
in metals will conclude the overview of spectroscopic X-ray imaging measurements in the field of
structure and dynamics of matter.
Zinnober (HgS) ist neben Eisenoxiden (Fe2O3 oder FeOOH) das am häufigsten verwendete mineralische Rotpigment. Die relativ seltenen Vorkommen in der Natur wurden schon in der Vorgeschichte abgebaut und in Gräbern und auf Felsmalerei als rote Farbe verwendet. In Asien spielt Zinnoberrot als Schreibtusche eine wichtige Rolle. Besonders zur Zeit des Buddhismus findet sich das Rot verstärkt auch auf Wandmalerei und Statuen. Schon früh beherrschte man die synthetische Herstellung und Optimierung des Pigments mit Zusatzstoffen, so dass von einer regional unterschiedlichen Verarbeitung auszugehen ist. Auf Grund seiner physikalisch-chemischen Eigenschaften (gute Eindringtiefe, konservierende Wirkung) wurde das leuchtend rote Farbpigment auch als Handelsware genutzt.
Die Pigmentanalyse gibt Auskunft über
- kulturelle Vorkommen, die Nutzung von Zinnober als Rotpigment in einem bestimmten Kontext.
- natürliche Vorkommen, die Herkunft des Minerals entsprechend der regionalen Bildungsbedingungen.
- Werkstätten, die Herstellung als Farbpigment mit unterschiedlichen Techniken.
Vorgestellt werden rote Tinten und Tuschen auf Schriftstücken der Seidenstraßenkulturen mit Zinnober als charakteristisch für eine bestimmte Tradition in der Verwendung und möglicher Indikator für kulturellen Austausch. Die in unterschiedlichen Schriften und Sprachen erhaltenen Manuskriptfragmente gelangten Anfang des letzten Jahrhunderts von der Oasenstadt Turfan nach Berlin, wo sie entziffert und kulturhistorisch erforscht werden. Die chemische Zusammensetzung ihrer Rottöne wird differenziert und in Rückkopplung mit der historischen Klassifikation der untersuchten Objekte verglichen. Eine solche Identifizierung von Farbtypen kann zur Einordnung von Kulturobjekten fragwürdiger Herkunft herangezogen werden.
Concrete is known to be a very useful, flexible and durable construction material. However, due to excess load, fatigue, chemical processes, freeze-thaw or reinforcement corrosion concrete may suffer from degradation. If detected too late, repair is difficult and expensive.
The propagation of ultrasonic waves is influenced by changes in the properties and structure of the material, including, but not limited to, stress, temperature, moisture content and microcracking. Ultrasonic velocieties thus may serve as indicators for structural health. Traditional ultrasonic methods as transmission time of flight measurements are used since decades, but are not sensible enough to show subtle changes. Coda Wave Interferometry (CWI), originally developed in seismology to detect stress changes in the earth's crust uses the information in the late part of ultrasonic signals originating from multiple reflections and scattering. Since a few years it is used by several researchers for lab experiments on concrete.
Meanwhile specialized sensors to be embedded in concrete have been developed. We have conducted several lab and a few field experiments, which will be reported here. The capabilities and limitations of CWI are summarized.
In diesem Vortrag werden hochauflösende analytische Methoden für die Untersuchungen von zementgebundenen Baustoffen vorgestellt. Zum einen werden frühe Hydratationsprozesse in situ und mit hoher Zeitauflösung untersucht und die Einflüsse von polymeren Fließmittel und Stabilisierer auf die Erstarrungsverzögerung beobachtet. Zum anderen werden Phasenübergänge unter schädigenden Angriffen im Gefügeprofil auf µm-Skala verfolgt. Die Möglichkeit die Auswirkungen der niedrigen realen Konzentrationen von schädigenden Agenten zu identifizieren stellt ein großes Potential für die Schädigungsanalyse unter realen Bedingungen dar. Insgesamt haben die vorgestelletn analytischen Techniken ein großes Potential für die Analyse der Phasenentwicklung in zementgebundenen Baustoffen.
Spatial and temporal control of thermal waves by using DMDs for interference based crack detection
(2016)
Active Thermography is a well-established non-destructive testing method and used to detect cracks, voids or material inhomogeneities. It is based on applying thermal energy to a samples’ surface whereas inner defects alter the non-stationary heat flow. Conventional excitation of a sample is hereby done spatially, either planar (e.g. using a lamp) or local (e.g. using a focused laser) and temporally, either pulsed or periodical. In this work we combine a high power laser with a Digital Micromirror Device (DMD) allowing us to merge all degrees of freedom to a spatially and temporally controlled heat source. This enables us to exploit the possibilities of coherent thermal wave shaping. Exciting periodically while controlling at the same time phase and amplitude of the illumination source induces – via absorption at the sample’s surface - a defined thermal wave propagation through a sample. That means thermal waves can be controlled almost like acoustical or optical waves. However, in contrast to optical or acoustical waves, thermal waves are highly damped due to the diffusive character of the thermal heat flow and therefore limited in penetration depth in relation to the achievable resolution. Nevertheless, the coherence length of thermal waves can be chosen in the mm-range for modulation frequencies below 10 Hz which is perfectly met by DMD technology. This approach gives us the opportunity to transfer known technologies from wave shaping techniques to thermography methods. We will present experiments on spatial and temporal wave shaping, demonstrating interference based crack detection.
Mit dem KorroPad Verfahren ist es dem Anwender möglich den Zustand der Passivschicht nichtrostender Stähle auf sehr einfache und schnelle Weise einschätzen zu können. Das Verfahren eignet sich dazu, den Grad der Passivität in Abhängigkeit der Umgebungsbedingungen und der Zeit nachzuvollziehen. Dies ermöglicht dem Anwender und Verarbeiter von nichtrostenden Stählen, die Lagerungsbedingungen und –zeiten einer frisch bearbeiteten Stahloberfläche zu ermitteln, welche für die Ausbildung einer stabilen Passivschicht notwendig sind, bevor diese risikoarm eingesetzt werden kann. Wie die hier dargestellten Beispiele und auch weitere zahlreiche praktische Anwendungen gezeigt haben, eignet sich das KorroPad ebenfalls für die Identifikation kritischer Prozessparameter bei der Verarbeitung nichtrostender Stähle. Mit dem Verfahren lassen sich viele prozessbedingte Einflussfaktoren auf die Oberflächengüte wie auch auf den Werkstoff charakterisieren. Aufgrund der schnellen und einfachen Auswertung der Prüfergebnisse können positive wie auch negative Veränderungen hinsichtlich der Passivschichtstabilität zügig erkannt werden. Dies ermöglicht es dem Anwender schnell zu reagieren, um kritische Einflüsse zu korrigieren und um eine Optimierung von Inhouse-Prozessen durchzuführen. Weitere Einsatzgebiete sind im Bereich der Wareneingangs- und/oder Warenausgangskontrolle denkbar, überall wo es um die Frage der Passivschichtstabilität einer nichtrostenden Stahloberfläche geht.
Hydrogen can cause unexpected material failure under consideration of stresses (external/internal) during manufacturing, processing or service of the materials. This failure is mostly based on a certain degradation of the mechanical properties. Thus, the correlation of hydrogen trapping vs. a respective microstructure is necessary for high strength steels. Thus, the scope of this work is the improvement of existing hydrogen trap models by verification of activation energies for hydrogen traps as well as the influence of the determination method. In this scope, the thermal desorption method is appropriate to distinguish between different hydrogen traps. Nevertheless, the specimen temperature has to be accounted very carefully in case of calculating the necessary trap energy.
Coating, stabilization layers, functionalization of particles or simple contamination are common variants of a core-shell system. For smaller nanoparticles this is of major importance. A particle with 16 nm diameter and a usual surface layer of 2 nm will have the same volume for the core as for the shell. In this case the material of the particle doesn’t have a clear definition. It is a common case that a particle consists of four different layers: Core, shell, stabilization layer and contamination. The properties of the particles differ according to this structure. For example silver particles might have a different dissolution rate for pure particles and for particles which are grown on top of a core.
Different solubility or defined other properties of materials is a common reason for producing core-shell systems. Gold cores are surrounded by silica to stabilize them or to get a defined distance between the cores. Silica might be surrounded by gold and the silica dissolved afterwards. This delivers hollow shells. Another important example for core-shell systems are quantum dots. A small core is surrounded by a different material for increasing the photoluminescence. Furthermore there a stabilization layer is needed. The smallest part of the final particles is the initial core. The photoluminescence is based on this core, but the shells contain much more material. Categorization should address this.
Core-shell systems are not covered by most of the existing decision trees for grouping. They are either regarded as special case or a singular layer. This disqualifies core-shell systems for grouping within the common models. There might be a very easy way to avoid this problem and even to combine some of the different decision trees. Starting the decision tree with the solubility of the outer shell and subsequently addressing the inner layers will be a pragmatic approach to solve the problem. If there is no shell, the categorization can start with a tiered approach or with the proposed “stawman” chemical categorization. If a shell is covering the surface there is a need to check if the shell is stable. If it is stable, the particle can be categorized based on this shell. If it is soluble, the ions need to be addressed as in the classic case. Furthermore the shell might increase the uptake by the cells. If the ions and the uptake are not critical the categorization can continue with the next layer.
With this not perfect but pragmatic approach, the surface layers can be addressed with very limited additional efforts. Most criteria are based on classically tabulated data. Including a rating system like the precautionary matrix approach might even address the fact that some parameters are not always Yes/No, e.g. solubility, ion toxicity and uptake.
Influence of the of dealumination and porosity on the acid sites of natural zeolite clinoptilolite
(2016)
Heavy feedstock from crude and bio oil is a widely available and renewable resource for production of fuel and starting materials for other organic valuables by cracking or hydrocracking. Catalytic processing of heavy feedstock can meet the increased demand of energy up to a great extent. It requires the application of acidic catalysts like zeolites. However, the used synthetic catalysts are difficult to recover and reuse and are mostly spent.
The use of natural zeolite as spent catalysts may open new perspectives in the chemical use of heavy feed feedstock by chemical conversion. Natural zeolites are not expensive, widely available and environment friendly. Clinoptilolite is the most abundant natural zeolite. Clinoptilolite has a crystalline structure with a defined micropore system of medium size showing unique ion exchange and sorption properties. However, it is catalytically active only in the H-form. Also certain porosity is required for improvement of the accessibility of active sites.
This paper deals with the tuning of acid properties and of the mesoporosity of the clinoptilolite by variation of the Si/Al framework ratio, extra-framework aluminum and modification of the porosity by specific acid and water vapor treatment. The preparation of hierarchical pore structures containing interconnected micro-meso-macropores is an important factor influencing the catalytic performance.
The obtained materials have been characterized by XRD, TEM, FTIR, Raman, TG/DSC. The chemical composition has been determined by ICP-AES. The porosity have been investigated by nitrogen adsorption desorption measurements. The acidity has been measured by Ammonia-TPD. The extent of dealumination, stability of the clinoptilolite against acid treatment and the change in the nature of acid sites and their local structure has been studied by solid state 29Si and 27Al MAS NMR spectroscopy in detail. The catalytic activity has been investigated in the acetalization of benzaldehyde with 1,3-butanediol. The impact of the porosity, change of the Si/Al ratio as well as present Al species on catalytic properties will be discussed.
k-values (k-ratio, K-value) is defined as ratio of the X-ray photon intensity I measured for a particular characteristic peak from the unknown sample to the value measured for the same X-ray peak from a reference material of known composition under identical conditions of beam energy, spectrometer efficiency and electron dose.
Mechanochemistry is a convenient way to form metal phosphonates with neutral and/or monodeprotonated phosphonates, controlled by the stoichiometric. In situ investigation of reactions helps understanding mechanisms and formation of intermediates. The knowledge of intermediates helps to find metastable structures.The diffusion mechanism is most probable for the mechanochemical synthesis of metal phosphonates.
Milling reactions often result in 100% yields of single products, making purifying procedures obsolete. Mech-anochemistry is also a sustainable and eco-friendly method. The ever increasing interest in this method is contrasted by a lack in mechanistic understanding of the mechanochemical reactivity and selectivity. Recent in situ investigations provided direct insight into formation pathways. However, the currently available theories do not predict temperature T as an influential factor. Here, we report the first determination of an activation energy for a mechanochemical reaction. In a temperature-dependent in situ study the cocrystallisation of ibuprofen and nicotinamide was investigated as a model system. These experiments provide a pivotal step towards a comprehensive understanding of milling reaction mechanisms.
CCQM has established a framework of comparisons to demonstrate the international comparability of chemical measurements. The key point is the establishment of comparable measurements, with traceability to internationally or nationally stated references. The Surface Analysis Working Group (SAWG) has been formally founded in 2003. CCQM ratified the group as a full working group of CCQM in April 2003 with these terms of reference:
- to develop pilot studies and carry out key comparisons of national measurement standards for surface and micro/nano-analysis;
- to assist in identifying and establishing inter-laboratory work to improve the traceability of surface and micro/nano-analysis;
- to establish and update a work plan to be adopted by CCQM;
- to discuss and review the scope of the working group and to liase with other working groups related to nanotechnology.
Following the 2015 meeting of the CCQM, the pilot study CCQM-P130 “WD and ED Electron Probe Micro Analysis on Au-Cu alloys” lead by BAM&NIST has been finalized. The Key Comparison K-129 “Measurement of atomic fractions in Cu(In,Ga)Se2 Films” lead by KRISS has made substantial progress and is about to be finalized. The new Key Comparison K-136 on “BET specific surface of ” lead by UNIIM&BAM has made strong progress in 2015 and will be finished in 2016.
The implementation of new 2-D materials based technologies in production processes requires the development of quality management tools. These have to be underpinned by appropriate measurements. Consequently there is a need for the development of the metrology for measurement methods, the development of certified reference materials (CRM) and finally standardization. This chain represents the ideal way to practically useful standards. The presentation will give an overview on the main players in the field and summarize the recent status of activities. At the highest level the metrology of chemical characterization of 2D materials is in the scope of the International Meter Convention, specifically the Consultative Committee for Amount of Substance: Metrology in Chemistry and Biology (CCQM). Pre-standardization is an activity field of the Versailles Project on Advanced Materials and Standards (VAMAS). Standardization is mainly addressed by addressed ISO Technical Committees. A summary on available CRMs relevant to the characterization of nano materials has been prepared by BAM. Examples from the work of BAM’s Division 6.1 “Surface Analysis and Interfacial Chemistry” showcasing the characterization of chemically modified graphene surfaces are given and specific needs for the development of metrology are addressed.
In the discussion the audience is invited to define specific needs which will be streamlined to the respective bodies!
We aim at preparing, characterising, and applying SURMOFs incorporating electro-active and -switchable mechanically interlocked molecules such as rotaxanes as the basis of functional devices.
Preparation and Positioning
Synthesis, purification and analytical characterization of electro-switchable rotaxanes suitable for SURMOF-formation as well as Layer-by-Layer assembly on surfaces.
Controlled deposition of electro-active SURMOFs and Layer-by-Layer self-assembled multilayers based on these switchable rotaxanes.
Construction of SURMOFs on micro-patterned surfaces.
Structural Characterisation and Physico-Chemical Properties
Electrochemical characterization of these rotaxanes in solution with cyclic voltammetry, chronoamperometry and impedance spectroscopy.
Surface characterization of SURMOFs and multilayers with XPS, NEXAFS, AFM, contact-angle measurements, transmission UV/Vis, ToF-SIMS and – in cooperation with partners from SPP – XRD.
Development of ToF-SIMS (also assisted by Principle Component Analysis of the fragment-ion data) as a method for imaging and depth-profiling.
Development of an appropriate electrochemical cell to perform cyclic voltammetry, chronoamperometry and impedance spectroscopy with SURMOFS and multilayers as working electrodes in a three-electrode cell.
Comparison of the structural and electrochemical properties of the redox-active unit in solution, multilayers and SURMOF focusing on the advantages of SURMOFs.
System Integration and Function Demonstration
Examination of the usability of the electroactive SURMOFS as optoelectronic switch or data storage device with a focus on the robustness of the system.
Usage of the SURMOFs as functional electrodes for electrochemical application.
Selective switching of ordered nanostructures to translate molecular motion to macroscopic property changes.
Charge separation in liquid droplets within a strong electric field leads to opposite directed progeny droplet jets. That phenomenon is called field induced droplet ionization (FIDI). The jets contain charged molecules, which enables a mass spectrometric analysis. Acoustic levitation of droplets has matured to a powerful tool for containerless sample handling in micro fluidic systems in order to suppress agglomeration and classic contamination pathways. Herein we present the combination of both: FIDI assisted By Ultra-Sound (FIDIBUS). Compared to FIDI, it felicitates a steady observation of a single droplet during its jet formation. Furthermore, it allows for using different shaped electrodes and a multiple droplet interrogation.
To understand the metabolic fate of food relevant mycotoxins in vitro systems were mainly used as the method of choice, so far. Yet, in recent years coupling of electrochemistry mass spectrometry (EC-MS) gained increasing importance as promising technique for fast simulation of metabolic processes and was successfully applied in particular for drug metabolism [1].
The aim of our work was to investigate the potential of EC-MS to predict phase I metabolites of priority mycotoxins and to compare the results with in vitro experiments. Hence, the EU-regulated Fusarium mycotoxins zearalenone (ZEN) and patulin as well as dihydroergocristine (DHEC) as model compound of ergot alkaloids were electrochemically oxidized and analyzed by EC MS for the first time.
Electrochemical conditions were set-up individually for each of the three mycotoxins. By using a coulometric flow through cell with a diamond working electrode oxidation of the chosen mycotoxins was observed after applying potentials between 1.7 and 2.0 V vs. Pd/H2. The electrochemically generated reaction products were analyzed online by mass-spectrometric detection.
All of the three chosen mycotoxins were electrochemically converted to mono- and/or dihydroxylated products confirming the results of ZEN related metabolism studies [2, 3] and in case of DHEC own results from in vitro assays. Due to a lack of metabolism studies concerning the oxidative fate of patulin, interpretation of EC-MS data and performing microsomal studies is of particular relevance.
Beside the identified products from electrochemical oxidation of ZEN, patulin and DHEC there is still a number of yet unknown compounds. Additional structural characterization of detected compounds by NMR and X-ray analysis will be facilitated by their large-scale production using preparative EC cells.
In this contribution the particle sizing techniques evaluated in NanoDefine are presented together with recommendations for their application/implementation on real-world materials. The experimental evaluation is discussed based on examples on NanoDefine materials. A systematic study on volume specific surface area as derived from BET measurements versus electron microscopy on powdered materials is also presented.
The international Qumran project coordinated at the BAM, Berlin, resulted in an integrated methodology for determining the original and acquired properties of the skin-based writing surfaces of the Dead Sea Scrolls. This methodology offers a powerful tool for addressing such questions as the provenance, sorting and comparison of manuscripts. In addition, we have developed specific protocols for on-site studies, which were successfully applied to the fragments from the Schøyen collection in Norway. Our studies show that the Dead Sea Scrolls writing surfaces can be divided roughly into three groups: leather, parchments of a light tint, and those of various shades of brown. The latter ones are invariably tanned, whereas the middle group is characterized by the presence of various inorganic salts. Some of the pale parchments, among them the Temple Scroll (11Q19), are remarkably similar to medieval European parchment. Therefore we have formulated the working theory that in the Judaea of the Hellenistic period two different parchment-making traditions existed side by side: an ‘eastern’ one (represented by the tanned parchments of Qumran, closely resembling Aramaic documents from the fifth century BC, and a ‘western’ one (represented by the untanned/lightly tanned ones similar to early Christian Greek parchments).
This division has found support during our first pilot study of the Geniza fragments, in which Babylonian and Palestinian traditions seem to follow the “eastern” and “western” technologies, respectively.
The evolution and socio-geographic distribution of writing inks in late Antiquity and the early Middle Ages build the second focus of the BAM group. We use X-ray fluorescence analysis (XRF) to determine the chemical composition of the inks and NIR-reflectography for their typology. Here the early appearance of the metal containing inks clearly belongs to the western tradition as opposed to the continuous use of soot inks in the East.
The lecture will discuss the sensitive issue of authentication of the objects of cultural heritage of immense cultural and monetary value if certified to be genuine. It will be made clear that material analysis alone, especially its non-destructive variety conducted by specialists in a single technique, can not prove that the object is genuine. The best material analysis can do, after all appropriate tests have been conducted, is to announce that nothing has been found that contradicts the assumption of genuineness. Moreover, the results of the natural analysis can never be used as the only justification of the authentication in the cases of composite objects such as manuscripts or epigraphs. A certification always requires the expertise of the specialist in the field (be it a historian, paleographer, epigrapher, etc.), whose judgment can be at the most supported by appropriate material analysis.
The most effective approach for testing suspicious artifacts has been established by the forensic science. Here, not the authentication, but the determination of the forgery stands in the focus of the work. Investigation protocols developed within 150 years and constantly improved include a clear statement of the analysis purpose and the definition of plausibility criteria for the possible outcome. The younger sister of the forensics, archaeometry has to overcome additional obstacles such as the heterogeneity of historic material coupled with the scarcity of suitable reference material. Over the last two decades the popularity of archaeometric studies has increased enormously, with the industry-driven development of so-called non-destructive technologies (NDT) that do not require sampling. Further technological developments led to the appearance of NDT methods with extremely small interaction windows (µm range). Each of these methods has limitations that have to be carefully considered when planning the tests of a heterogeneous and often partially degraded historical material. This approach is inherently multi-instrumental, therefore archaeometric and forensic departments unite a number of specialists who work together defining the tasks and the methods involved for their successful completion.
The experimental knowledge about the inks of antiquity and late antiquity rarely goes beyond their visual description. In rare cases, inks typology has been determined by means of microscopy and reflectography, i.e. using their physical and optical properties, respectively. Soot, plant, and iron gall inks form different typological classes of historical black writing materials. Soot ink is a fine dispersion of carbon pigments in a water-soluble binding agent; plant-based ink consists of tannin solution; iron gall-ink presents a boundary case between soot and plant ink— a water soluble preliminary stage (similar to inks from the second group) oxidizes and evolves into a black, insoluble material (similar to the carbon pigments of the first group) when the writing is exposed to air. Each ink class has distinct properties that would readily permit their easy differentiation, if only these historical inks always belonged to just one of the classes above. In reality, inks may contain additives that obscure a clear picture.
All the black inks of the DSS have been hitherto identified as soot inks. Yet some manuscripts, with 1QapGen ar among them, display ink corrosion that is incompatible with the pure soot ink. This type of corrosion commonly observed in medieval manuscripts written with iron gall inks, results from the catalytic action of metallic component in the ink. Early analysis of this ink conducted by Nir El and Broshi in 1996 found copper in the corrosive inks and attributed its presence to the use of bronze inkwells. Re-investigation of the 1QapGen ar ink suggests, however, that the ink composition, soot + copper, agrees well with the ink recipe recorded in the 1st century CE by Dioscorides. Similar inks have been already attested on contemporary Egyptian papyri. The first part of the paper is dedicated to the new results on the inks and corrosion pattern of the 1QapGen ar.
In the second part of the presentation I will focus on the luxury scrolls, a distinct codicological type introduced by E. Tov. Our studies show that the preparation of the writing materials cannot supplement the list of codicological criteria offered by Tov. Therefore, one can divorce the writing material production from its inscription in contrast with the medieval scriptoria practices that included parchment production and copying of the manuscripts.
Material study of inks
(2016)
Our experimental knowledge about the inks of antiquity and late antiquity rarely goes beyond their visual description. In rare cases, inks typology has been determined by means of microscopy and reflectography, i.e. using their physical and optical properties, respectively. Soot, plant, and iron gall inks form different typological classes of historical black writing materials. Soot ink is a fine dispersion of carbon pigments in a water-soluble binding agent; plant-based ink consists of tannin solution; iron gall-ink presents a boundary case between soot and plant ink— a water soluble preliminary stage (similar to inks from the second group) oxidizes and evolves into a black, insoluble material (similar to the carbon pigments of the first group) when the writing is exposed to air. Each ink class has distinct properties that would readily permit their easy differentiation, if only these historical inks always belonged to just one of the classes above. In reality, inks may contain additives that obscure a clear picture.
Even crude observations suggest that the inks of antiquity differed greatly in their composition. We believe, that reconstructing the ink recipes with the help of advanced non-destructive analytical techniques could serve as a powerful accessory in the studies of ancient papyri.
The proposed paper will present a short survey of the methods of material analysis and the challenges offered by ancient inks. (Two) examples of ink studies from the collections of the Israel Museum in Jerusalem and Egyptian Museum in Berlin will conclude the paper.
The presentation shows how the three-dimensional quantification of dislocations and their characteristic features, e.g. Burgers vector, line direction, dislocation density, is carried out at the transmission electron microscope in scanning mode (STEM) at Division 5.1 at BAM. Exemplarily, the methods are shown for Ni-base superalloy single crystals, for which a short introduction is given using further TEM techniques. Additional examples on low angle grain boundaries, nucleation of oxides at dislocations and interaction of dislocations and carbides are shown.
The content of the presentation was addapted, aiming at scientists who work within the DFG Priority Programme 1713 "Strong coupling of thermo-chemical and thermo-mechanical states in applied materials".
The performance of a miniaturized channel for the separation of polymer and metal nanoparticles (NP) using Asymmetrical Flow Field-Flow Fractionation (AF4) was investigated and compared with a conventional AF4 system. To develop standard separation methods, experimental parameters like cross flow, gradient profile and injection time were varied and optimized. Corresponding chromatographic parameters were calculated and compared. Our results indicate that the chromatographic resolution in the miniaturized channel is lower, whereas significantly shorter analyses time and less solvent consumption were obtained. Moreover, the limit of detection (LOD) and limit of quantification (LOQ) obtained from hyphenation with a UV-detector are obviously lower than in a conventional channel, which makes the miniaturized channel interesting for trace analysis.