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Since a few years the direct detection of X-ray photons into electrical signals is possible by usage of highly absorbing photo conducting materials (e.g. CdTe) as detection layer of an underlying CMOS semiconductor X-ray detector. Even NDT energies up to 400 keV are possible today, as well. The image sharpness and absorption efficiency is improved by the replacement of the unsharp scintillation layer (as used at indirect detecting detectors) by a photo conducting layer of much higher thickness. If the read-out speed is high enough (ca. 50 – 100 ns dead time) single X-ray photons can be counted and their energy measured. Read-out noise and dark image correction can be avoided. By setting energy thresholds selected energy ranges of the X-ray spectrum can be detected or suppressed. This allows material discrimination by dual-energy techniques or the reduction of image contributions of scattered radiation, which results in an enhanced contrast sensitivity. To use these advantages in an effective way, a special calibration procedure has to be developed, which considers also time dependent processes in the detection layer. This contribution presents some of these new properties of direct detecting digital detector arrays (DDAs) and shows first results on testing fiber reinforced composites as well as first approaches to dual energy imaging.
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.
In this paper, we identify the strategic motives of German manufacturing companies in the electrical engineering and machinery industry to be involved in standards development organizations. First, we present the general motives for the formation of strategic alliances and relate them to specific standardization motives. Then, we identify pursuing specific company interests, solving technical problems, knowledge seeking, influencing regulation, and facilitating market access as motives to standardize by means of factor analysis. In a second step, we test hypotheses on the relationship between the importance of strategic motives and firm level variables, e.g. R&D intensity, innovation activities, and firm size. The results reveal that firms in electric engineering and machinery have a particularly strong interest in ensuring industry-friendly design of regulations, which can be achieved by standards. Moreover, the results confirm that small firms also from these two sectors are active in standardization alliances to access knowledge from other involved stakeholders.
Self-assembling biomolecules provide attractive templates for the preparation of metallic nanostructures. However, the intuitive transfer of the “outer shape” of the assembled macromolecules to the final metallic particle depends on the intermolecular forces among the biomolecules which compete with interactions between template molecules and the metal during metallization. The shape of the bio-template may thus be more dynamic than generally assumed. Here, we have studied the metallization of phospholipid nanodiscs which are discoidal particles of ~10 nm diameter containing a lipid bilayer ~5 nm thick. Using negatively charged lipids, electrostatic adsorption of amine-coated Au nanoparticles was achieved and followed by electroless gold deposition. Whereas Au nanoparticle adsorption preserves the shape of the bio-template, metallization proceeds via invasion of Au into the hydrophobic core of the nanodisc. Thereby, the lipidic phase induces a lateral growth that increases the diameter but not the original thickness of the template. Infrared spectroscopy reveals lipid expansion and suggests the existence of internal gaps in the metallized nanodiscs, which is confirmed by surface-enhanced Raman scattering from the encapsulated lipids. Interference of metallic growth with non-covalent interactions can thus become itself a shape-determining factor in the metallization of particularly soft and structurally anisotropic biomaterials.
We describe a fast and effective synthesis for molecular metal phosphonates. Isomorphic compounds [M(II)(HO₃PPh)₂(H₂O₃PPh)₂(H₂O)₂] (M = Mn (1), Co (2), Ni (3); Ph = C₆H₅) were obtained by grinding. The complexes are mononuclear compounds containing neutral and monodeprotonated phenylphosphonic acid and water as ligands. The crystal structures were determined using powder X-ray diffraction (PXRD) data and validated by extended X-ray absorption fine structure (EXAFS) data. Combined synchrotron XRD measurements and Raman spectroscopy were conducted for investigating the reactions in situ. Based on these data, the intermediates were characterized and the formation mechanism was derived.
Einfluss der Porosität von Beton auf den Ablauf einer schädigenden Alkali-Kieselsäure-Reaktion
(2016)
This thesis deals with the question of how the porosity of concrete influences the process of a damaging alkali-silica-reaction (“ASR”). In particular, it is examined whether the use of slip form pavers and the reduced porosity resulting from this use have an effect on the process of a damaging ASR.
Since the 1980s slip form pavers have been used, which modifies the structure of concrete. However, these modifications have not yet been taken into consideration in the relevant technical guidelines. The use of slip form pavers instead of conventional concrete pavers results in a denser structure. Due to the denser structure the ductility and the porosity of the concrete decrease. Thus it is more difficult for the tensile stress to be reduced. Moreover, the space for the ASR gel to expand is reduced. These consequences promote the ASR. By contrast, the permeability of the concrete is lower. Hence, the penetration of external alkalis is reduced and the diffusion of the alkalis to the potentially reactive aggregate slowed down. Against this background the question arises whether the use of slip form pavers and the reduced porosity of the concrete increase the risk of a damaging ASR.
An innovative non-destructive testing methodology is applied to answer this question. Based on variations of the porosity it is examined which damage parameters influence the process and intensity of a damaging ASR. The damaging parameters taken into consideration are the mechanical properties of the concrete, the expansion space and the transport processes within the concrete. In order to determine the influence of the relevant damaging parameters two categories of tests are conducted: one category is based on a high internal potential for damages due to ASR, the other one on a high external potential. In both cases alkali-reactive slow/late aggregates are tested. The different porosities of the concrete mainly result from a variation of the w/c-ratio. In case of a high internal potential for ASR-damages the mechanical properties and the expansion space play the most important role. Furthermore; the influence of an air-entraining agent on the process of a damaging ASR is taken into account. The high internal potential for ASR-damages is provoked by the use of cement with a high amount of alkalises for the production of the concrete samples. These samples are stored in the 40 °C fog chamber storage and the 60 °C concrete prisms test. On the one hand the expansion and the change in mass as well as the eigenfrequency are measured discontinuously in the conventional way. On the other hand the innovative testing methodology applied to these ASR-provoked stored concrete samples serves to continuously measure the expansion and the hardening as well as crack formation processes. This methodology comprises a determination of the ultrasonic velocity and of acoustic emissions as well as 3-dimensional micro X-ray computed tomography (μ-3D-CT). The high external potential for ASR-damages is provoked by the cyclic climate storage, designed by FIB. The analysis of these concretes focuses on transportation processes.
A combined analysis of EXAFS and Raman spectra is applied for the study of
InxGa1-xN alloys with 0.3<x<0.5. Alloying causes relaxation of the selection rules resulting in
Raman spectra that resemble the vibrational density of states. On the other hand, theoretical
simulation of the Raman spectra using the Equation of Motion routine of FEFF8 provides the
vibrational component of the Debye-Waller factor (DWF). The static disorder component of
the DWFs was obtained by fitting the Ga and In K-edge EXAFS spectra. The analysis revealed
that the nearest neighbor distances of the 1st and 2nd shell deviate from the values predicted by
the law of Vegard and the virtual crystal approximation. The static disorder in the first nearest
neighboring shell (In-N and Ga-N) is null whereas in the cation-cation neighboring shells the
static component is generally smaller than the vibrational.
The successful mechanochemical syntheses of three cadmium phenylphosphonates indicates that mechanochemistry is ideally suited for synthesizing metal phosphonates. With this powerful synthesis tool it is possible to synthesize rapidly and efficiently both known and novel phosphonates. The Crystal structures of the two new compounds, and, were solved from PXRD data. They contain monodeprotonated phenylphosphonate and neutral phenylphosphonic acid ligands. The synthesis pathways of all three compounds were investigated in situ. A diffusion mechanism is corroborated by our findings.
Intermediates could be detected and identified. The kinetically favored product (3) could always be detected during the syntheses. The thermodynamic stability of the compounds and the stoichiometric ratio of the starting materials are the two directing factors for the synthesis of the final products.
The folding of single-stranded telomeric DNA into guanine (G) quadruplexes is a conformational change that plays a major role in sensing and drug targeting. The telomeric DNA can be placed on DNA origami nanostructures to make the folding process extremely selective for K+ ions even in the presence of high Na+ concentrations. Here, we demonstrate that the K+-selective G-quadruplex formation is reversible when using a cryptand to remove K+ from the G-quadruplex. We present a full characterization of the reversible switching between single-stranded telomeric DNA and G-quadruplex structures using Förster resonance energy transfer (FRET) between the dyes fluorescein (FAM) and cyanine3 (Cy3). When attached to the DNA origami platform, the G-quadruplex switch can be incorporated into more complex photonic networks, which is demonstrated for a three-color and a four-color FRET cascade from FAM over Cy3 and Cy5 to IRDye700 with G-quadruplex-Cy3 acting as a switchable transmitter.
Analytische bruchmechanische Ermittlung der Schwingfestigkeit von Schweißverbindungen (IBESS-A3)
(2016)
Ziel des DFG-AiF-Forschungsclusters IBESS war die Entwicklung einer Methodik zur bruchmechanischen Ermittlung von Wöhlerkurven in Schweißverbindungen. Dem vorliegenden Teilprojekt A3 kamen dabei zwei Aufgaben zu: die Entwicklung einer analytischen bruchmechanischen Methodik und die Koordinierung des insgesamt acht Partner umfassenden Clusters. Dieser Bericht fasst die Ergebnisse der erstgenannten Aufgabe zusammen. Die bruchmechanische Methode ist durch folgende Aspekte charakterisiert. (a) Sie beschreibt sowohl Kurz- als auch Langrisswachstum. Ersteres umfasst mechanisch und physikalisch kurze Risse. Mechanisch kurze Risse weisen Abmessungen in der Größenordnung der plastischen Zone auf, weshalb sie zwar bruchmechanisch, nicht jedoch auf der Basis des linear-elastischen K-Konzepts charakterisiert werden können. Im Projekt wurde entsprechend eine Methode zur Bestimmung eines „plastizitätskorrigierten“ zyklischen K-Faktors entwickelt, die auf dem zyklischen J-Integral beruht. Physikalisch kurz bedeutet, dass die Rissschließeffekte im Ausgangsstadium der Rissentwicklung zunächst noch nicht vorhanden sind, dann jedoch graduell aufgebaut werden, bis sie mit Erreichen des Langrissstadiums eine risstiefenunabhängig konstante Größe erreichen. Beschrieben wird dieser Effekt durch die Anwendung der sogenannten zyklischen R-Kurve, der Funktion des Schwellenwerts gegen Rissausbreitung von der Risstiefe. Mittels Rissarrestbetrachtungen des kurzen Risses werden (b) die Ausgangsrissgröße für die weitere Bruchmechanikanalyse und (c) die für N = 107 definierte Dauerfestigkeit der Bauteile bestimmt. Die Analyse erfolgt (d) statistisch, Schwankungen der lokalen Nahtgeometrie entlang des Nahtübergangs über ein Modell äquidistanter Abschnitte einbezogen werden. (e) Eigenspannungen werden sowohl im unbehandelten Schweißzustand als auch nach zyklischer Belastung berücksichtigt. Das Modell wird an insgesamt 33 Wöhlerkurven validiert, die an drei Schweißverbindungsformen (Stumpfstoß, Kreuzstoß, Längssteife) mit je zwei unterschiedlichen Ausführungen, zwei Werkstoffen (S355NL und S960QL), sowie im spannungsarmgeglühten und ungeglühten Zustand experimentell ermittelt wurden.