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Photophysical and mechanistic studies, the comparison of different emitter classes, and the rational design of the next generation of molecular and nanoscale reporters require quantitative photoluminescence measurements and the reliable determination of the key performance parameter photoluminescence quantum yield (QY), i.e., the number of emitted per absorbed photons. This is of special importance for all photoluminescence applications in the life and material sciences in the UV/vis/NIR/SWIR. To improve the reliability and comparability of photoluminescence and QY measurements across laboratories, pitfalls, achievable uncertainties, and material-specific effects related to certain emitter classes must be explored. Also, suitable protocols and reference materials are needed which have been validated in interlaboratory comparisons for different wavelength regions and transparent and scattering luminophores.[1] Based on absolute and relative photoluminescence measurements of functional dyes and nanomaterials like semiconductor quantum dots and rods, spectrally shifting lanthanide upconversion nanocrystals, perovskites, and YAG:Cer converter materials, reliable methods for determining QY of transparent and scattering luminophores, nonlinear emitters, and solid luminescent nanomaterials have been developed.[2,3] Thereby, material- and method-related uncertainties of relative and absolute QY measurements and achievable uncertainties could be quantified for linear and nonlinear UV/vis/NIR/SWIR emitters and lately for also luminescent and scattering materials and solid phoshors, here in an interlaboratory comparison of three labs utilizing integrating sphere spectroscopy.[4,5] In addition, to provide simple tools for a better comparability of QY measurements, recently, a first set of UV/vis/NIR quantum yield standards has been developed and certified with complete uncertainty budgets.[6] In the following, the outcome of these studies will be presented, thereby addressing common pitfalls and providing recommendations on the performance of reliable QY measurements of linear and non-linear emitters in transparent, scattering, and solid samples.
Reversible polycondensations are polycondensations that include equilibration reactions at any stage of the process. Syntheses of Polyesters in bulk involving transesterification reactions and syntheses of polyamides in bulk involving transamidation are typical examples. In 1950, Jacobson and Stockmayer published a first theory of reversible polycondensations based on experimental studies with aliphatic polyesters.[1,2] They explained the reversibility by the reversible formation of cyclic oligomers and low molar mass polymers from an active chain end (so-called “back-biting”). The formation of cycles via end-to-end cyclization was excluded in agreement with Flory´s theory of irreversible polycondensations.[3] The reinvestigation of the Jacobson-Stockmayer experiments by the authors in combination with theoretical considerations shows that the JS theory is wrong. [4,5] It turned out that the experimental scenario is far from the reality. In real polycondensations, intermolecular equilibration is faster than “back-biting”, and end-to-end cyclization is quite normal. The revised theory of step-growth polymerization predicts that in the ideal case of 100% conversion, all reaction products are cycles, regardless, of whether the step-growth polymerization is reversible or not.
Photophysical and mechanistic studies, the comparison of different emitter classes, and the rational design of the next generation of molecular and nanoscale reporters require quantitative photoluminescence measurements and the reliable determination of the key performance parameter photoluminescence quantum yield (QY), i.e., the number of emitted per absorbed photons. This is of special importance for all photoluminescence applications in the life and material sciences in the UV/vis/NIR/SWIR.
UFP-Emission beim 3D-Druck
(2024)
Desktop-3D-Drucker haben in der letzten Dekade große Popularität in Bildungseinrichtungen, kleinen Unternehmen und Privathaushalten erlangt. Weit verbreitet ist mittlerweile die „Fused Filament Fabrication (FFF)“ Technologie. Hier wird ein thermoplastisches Filament geschmolzen, durch eine Metalldüse extrudiert und anschließend schichtweise so auf ein Druckbett aufgetragen, dass ein 3D-Objekt entsteht. Das Filamentmaterial wird dabei thermisch stark belastet, was zur Emission von Aerosolen sowie flüchtigen organischen Verbindungen (VOC) führt. Dabei werden hauptsächlich ultrafeine Partikel (UFP, dP < 100 nm) freigesetzt werden, die sogar in manchen Fällen im sub-4nm Größenbereich einen signifikanten Anteil ausmachen können (Tang und Seeger 2024).
Die gesundheitliche Relevanz eingeatmeter UFP ist durch sehr viele Studien gut belegt. Während eines i.d.R. mehrstündigen FFF-Druckvorgangs wird ein Anwender mit diesen Luftschadstoffen im Innenraum exponiert, häufig ohne eine Einschätzung des damit verbundenen Risikos zu haben. Die Exposition kann durch technische Faktoren (z.B. Druckerausstattung und -einstellung, Innenraumventilation), aber auch erheblich durch die Filamentauswahl beeinflusst werden. Unser Vorschlag zur Risikominderung besteht in der Auszeichnung emissionsarmer Filamentprodukte mit dem Umweltzeichen „Blauer Engel“, um so den Verbrauchern eine fundierte Auswahl zu ermöglichen. In unserem Projekt entwickeln wir dafür ein kammerbasiertes, standardisierbares und robustes Prüfverfahren zur vergleichenden Messung der Emission aus Filamenten. Mit dem Strangdruck-Verfahren (engl. Strand Printing Method, SPM) wird eine festgelegte Filamentlänge mit konstanter Rate extrudiert und auf dem Druckbett abgelegt, ohne dabei ein 3D-Objekt aufzubauen. Diese Vorgehensweise reduziert den Einfluss experimentell schlecht zu kontrollierender Faktoren sowie die Ausfallquote. Eine detaillierte Beschreibung und die Vorteile von SPM werden in Tang und Seeger (2022) erläutert. SPM wurde bereits für 44 Filamentprodukte aus unterschiedlichen Polymeren und Additiven als Vergleichstest angewendet. Alle Messungen wurden in einer klimatisierten 1 m³-Emissionsprüfkammer durchgeführt. Die Gesamtanzahl der emittierten Partikel (TP) dient als Beurteilungsmaß, in Anlehnung an die Vergabegrundlage DE-UZ-219 des Umweltzeichens Blauer Engel für Laserdrucker. Unter den getesteten Filamentprodukten variiert TP um ca. vier Größenordnungen (1E+9 ≤ TP ≤ 1E+13). Auch innerhalb jeder der untersuchten Polymergruppen variierte TP signifikant. Die Partikelemission kann daher nicht allein nach dem Basispolymer kategorisiert werden. Unsere Resultate belegen, dass die Stärke der Partikelemission eher eine charakteristische und individuelle Eigenschaft eines Filamentproduktes ist. Die Herkunft der Polymere, die herstellerspezifischen Additive sowie die nicht deklarierte Verunreinigungen können einen starken Einfluss auf die Emission haben. Die Auszeichnung von emissionsarmen Filament-produkten verspricht somit eine einfache, aber effektive Maßnahme zu sein, um Verbrauchern eine Minderung des Expositionsrisikos beim FFF-3D-Druck zu ermöglichen.
Data-driven materials design aims to predict and optimize material properties, such as stability and thermal conductivity, which are influenced by vibrational behavior. Approaches like DFT are computationally demanding and have limitations for phonon calculations. Machine learning-driven interatomic potentials (MLIP), like the Gaussian approximation potential (GAP), offer a more efficient alternative.1–8 We developed a Python workflow to automate MLIP generation using the Materials Project database.9 DFT computations, MLIP fitting and benchmark steps are automated.10,11 This approach accelerates phonon calculations and supports testing different data generation strategies and hyperparameters, and further validation12 is planned. Our goal is to provide open-source code and share these potentials.
Resistance to carbonation and chloride migration are critical durability properties in cementitious construction materials. The ingress of CO2 and chlorides can lead to concrete deterioration and reinforcement corrosion, underscoring the importance of ensuring high resistance to these durability-reducing factors. Traditional methods, such as determinating the carbonation coefficient using standard procedures, are time-consuming and resource-intensive. These tests typically require 42 days of preconditioning, followed by 70 days before the final results can be determined using a phenolphthalein test, for a total duration of 112 days. In addition, some test chambers can only accommodate four samples at a time.
In this study, we investigate whether 1H NMR relaxometry can effectively predict not only the carbonation resistance, KAC,3%, but also the chloride migration coefficient, DRCM, and the compressive strength, fc, of concrete, providing a method that could potentially streamline and accelerate the material development process by directing us quickly to potentially well-suited formulations. We performed measurements on non-carbonated fully saturated concrete and mortar samples at 28, 56, and 92 days using the NMR tomograph at BAM (8.9 MHz). Notably, the NMR measurements taken at 28 days showed no significant differences, suggesting that this timeframe is sufficient for meaningful results. The samples analyzed were drill cores, each 70 mm in diameter and approximately 120 mm in height. The NMR features we focused on included the initial amplitude E0, the x and y values of the dominant T2 relaxation time, and the logarithmic mean of the T2 relaxation time distribution. Another key feature was the surface relaxivity, which was determined by comparing the NMR curves with results from mercury intrusion porosimetry. We examined the correlation of these NMR features with the aforementioned durability properties, which were determined in a laboratory on sister samples using standard procedures. No chloride migration tests were performed on the mortar samples, and the carbonation procedure was carried out unter atmospheric conditions.
The preliminary results show that the correlation factors for the NMR features with the carbonation coefficients of concrete were particularly remarkable. The strongest correlations were observed for the dominant relaxation time and the logarithmic mean, with values approaching 1. The preliminary results also indicate that there are high correlations between the compressive strength and amplitude-related features. In contrast, no strong correlations are observed for the DRCM. Although the results related to the mortar samples are still being analyzed, these initial correlations suggest that 1H NMR relaxometry could be a valuable tool for early assessment of material properties. Furthermore, the rapid and non-destructive nature of NMR measurements, requiring only a few minutes per sample, suggests that this technique has the potential to significantly accelerate the process of evaluating durability properties in cementitious materials. This capability also paves the way for the use of NMR features as input for AI-driven predictive models.
Following points are addressed in this contribution: Advantages of correlative analysis in electron microscopy; Measurement principle of the different electron microscopy modes used; Presentation of the nanomaterials used for this study; Role of sample preparation; and, with particular description, the Sequence kV-variation with InLens SE & transmission SEM detection of the same field-of-view.
Since laser powder bed fusion (PBF-LB/M) is prone to the formation of defects during the building process, a fundamental requirement for widespread application is to find ways to assure safety and reliability of the additively manufactured parts. A possible solution for this problem lies in the usage of in-situ thermographic monitoring for defect detection. In this contribution we investigate possibilities and limitations of the VIS/NIR wavelength range for defect detection. A VIS/NIR camera can be based on conventional silicon-based sensors which typically have much higher spatial and temporal resolution in the same price range but are more limited in the detectable temperature range than infrared sensors designed for longer wavelengths. To investigate the influence, we compared the thermographic signatures during the creation of artificially provoked defects by local parameter variations in test specimens made of a nickel alloy (UNS N07208) for two different wavelength ranges (~980 nm and ~1600 nm).
Powder bed technologies are amongst the most successful Additive Manufacturing (AM) techniques. The application of these techniques to most ceramics has been difficult so far, because of the challenges related to the deposition of homogeneous powder layers when using fine powders.
In this context, the "layerwise slurry deposition" (LSD) has been developed as a layer deposition method enabling the use of powder bed AM technologies also for advanced ceramic materials. The layerwise slurry deposition consists of the layer-by-layer deposition of a ceramic slurry by means of a doctor blade, in which the slurry is deposited and dried to achieve a highly packed powder. Not only very fine, submicron powders can be processed with low organics, but also the dense powder bed provides excellent support to the parts built.
The latest development of this technology shows that it is possible to print ceramic parts in a continuous process by depositing a layer onto a rotating platform, growing a powder bed following a spiral motion. The unique mechanical stability of the layers in LSD-print allows to grow a powder bed several centimeters thick without any lateral support. The continuous layer deposition allows to achieve a productivity more than 10X higher compared to the linear deposition, approaching a build volume of 1 liter/hour.
Hybrid additive manufacturing plays a crucial role in the restoration of gas turbine blades, where e.g., the damaged blade tip is reconstructed by the additive manufacturing process on the existing blade made of a parent nickel-based alloy. However, inherent process-related defects in additively manufactured material, along with the interface created between the additively manufactured and the cast base material, impact the fatigue crack growth behavior in bi-material components. This study investigates the fatigue crack growth behavior in bi-material specimens of nickel-based alloys, specifically, additively manufactured STAL15 and cast alloy 247DS. The tests were conducted at 950 °C with stress ratios of 0.1 and -1. Metallographic and fractographic investigations were carried out to understand crack growth mechanisms. The results revealed significant retardation in crack growth at the interface. This study highlights the potential contributions of residual stresses and microstructural differences to the observed crack growth retardation phenomenon, along with the conclusion from an earlier study on the effect of yield strength mismatch on crack growth behavior at a perpendicular interface in bi-material specimens.