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Paper des Monats
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Subsurface residual stresses (RS) were investigated in Ti-6Al-4V cuboid samples by means of X-ray synchrotron diffraction. The samples were manufactured by laser powder bed fusion (LPBF) applying different processing parameters, not commonly considered in open literature, in order to assess their influence on RS state. While investigating the effect of process parameters used for the calculation of volumetric energy density (such as laser velocity, laser power and hatch distance), we observed that an increase of energy density led to a decrease of RS, although not to the same extent for every parameter variation. Additionally, the effect of support structure, sample roughness and LPBF machine effects potentially coming from Ar flow were studied. We observed no influence of support structure on subsurface RS while the orientation with respect to Ar flow showed to have an impact on RS.We conclude recommending monitoring such parameters to improve part reliability and reproducibility.
While the volumetric energy density is commonly used to qualify a process parameter set, and to quantify its influence on the microstructure and performance of additively manufactured (AM) materials and components, it has been already shown that this description is by no means exhaustive. In this work, new aspects of the optimization of the selective laser melting process are investigated for AM Ti-6Al-4V. We focus on the amount of near-surface residual stress (RS), often blamed for the failure of components, and on the porosity characteristics (amount and spatial distribution). First, using synchrotron x-ray diffraction we show that higher RS in the subsurface region is generated if a lower energy density is used. Second, we show that laser de-focusing and sample positioning inside the build chamber also play an eminent role, and we quantify this influence. In parallel, using X-ray Computed Tomography, we observe that porosity is mainly concentrated in the contour region, except in the case where the laser speed is small. The low values of porosity (less than 1%) do not influence RS.
Connecting Diffraction-Based Strain with Macroscopic Stresses in Laser Powder Bed Fused Ti-6Al-4V
(2020)
The laser powder bed fusion (LPBF) production process often results in large residual stress (RS) in the parts. Nondestructive techniques to determine RS are badly needed. However, a reliable quantification of macro-RS (i.e., stress at the component level) by means of diffraction-based techniques is still a great challenge, because the link between diffraction-based strain and macro-RS is not trivial. In this study, we experimentally determine (by means of in-situ synchrotron radiation diffraction) this link for LPBF Ti-6Al-4V. We compare our results with commonly used models to determine the so-called diffraction elastic constants (DECs). We show that LPBF materials possess different DECs than wrought alloys, simply because their microstructural and mechanical properties are different. We also show that the existing models can be used to calculate DECs only if high accuracy of the RS values is not required. If the peculiarities of the microstructure have to be taken into account (as is the case of additively manufactured materials), a radically new approach is desirable.
The overview of the activity of group 8.5 Micro-NDT (BAM, Belin, Germany) in the field of additively manufacturing material characterization will be presented. The research of our group is focused on the 3D imaging of AM materials by means of X-ray Computed Tomography at the lab and at synchrotron, and the residual stress characterization by diffraction (nondestructive technique).
Most of the Al alloys used in additive manufacturing (AM), in particular Laser Powder Bed Fusion (LPBF), do not exceed a strength of 200 MPa, whereas conventionally high-performance alloys exhibit strengths exceeding 400 MPa. The availability of such Al alloys in AM is limited due to difficulties in printability, requiring synergetic material and AM process development to satisfy harsh processing conditions during LPBF [1]. One approach is the addition of reinforcement to the based powder, allowing tailoring composition and properties of a Metal Matrix Composite (MMC) by AM. Still, the effect of the reinforcement on the resulting mechanical properties must be studied to understand the performance and limits of the newly developed material. The goal of this work was to investigate the failure mechanism of LPBF Al-based MMC material using in-situ Synchrotron X-ray Computed Tomography (SXCT) during mechanical testing.
In this work, we present the recent in-situ imaging developments at the BAMline (of synchrotron BESSY II, HZB), focused on the in-situ characterization and understanding of microstructural evolution of additively manufactured materials subjected to different environments. Two show cases are presented. In the first, X-ray refraction radiography (SXRR) was combined with in-situ heat treatment to monitor the microstructural evolution as a function of temperature in a laser powder bed fusion (LPBF) manufactured AlSi10Mg alloy. We show that SXRR allows detecting the changes in the Si-phase morphology upon heating using statistically relevant volumes. SXRR also allows observing the growth of pores (i.e., thermally induced porosity), usually studied via X-ray computed tomography (XCT), but using much smaller fields-of-view. In the second case study, XCT was combined with in-situ tensile test to investigate the damage mechanism in a LPBF Aluminum Metal Matrix Composite (MMC). In-situ SXCT test disclosed the critical role of the defects in the failure mechanism along with pre-cracks in the reinforcement phase of MMC. We found that cracks were initiated from lack-of-fusion defects and propagated through coalescence with other defects.
Additive manufacturing technologies provide unique possibilities in the production of topologically optimized, near-net shape components. The main limiting factors affecting the structural integrity of Laser Powder Bed Fusion (LPBF) parts are manufacturing defects and residual stress (RS) because both of them are virtually inevitable. Taking into account the complex thermal history of LPBF materials, a prediction of the material behavior is not possible without experimental data on the microstructure, defect distribution, and RS fields. Therefore, this thesis aims to understand the factors that influence the LPBF Ti-6Al-4V material performance the most, covering both the production and the post-processing steps of manufacturing.
Indeed, a parametric study on the influence of manufacturing process and post-processing on RS, defects and microstructure was performed. It was found that the volumetric energy Density (EV), commonly used for the LPBF process optimization, does neither consider the pore shapes and distribution, nor the influence of individual parameters on the volume fraction of pores.
Therefore, it was recommended not to use EV without great care. It was shown that the Position on the base plate has a great impact on the amount of RS in the part.
The micromechanical behavior of LPBF Ti-6Al-4V was also studied using in-situ Synchrotron X-ray diffraction during tensile and compression tests. Diffraction elastic constants (DEC), connecting macroscopic stress and (micro) strain, of the LPBF Ti-6Al-4V showed a difference
from the DEC of conventionally manufactured alloy. This fact was attributed to the peculiar microstructure and crystallographic texture. It was therefore recommended to determine experimentally DECs whenever possible.
Low Cycle Fatigue (LCF) tests at a chosen operating temperature were performed to evaluate the effect of post-treatment on the mechanical performance. Through the information on the microstructure, the mesostructure, and the RS, the LCF behavior was (indirectly) correlated to the process parameters. It was found that the fatigue performance of LPBF samples subjected to hot isostatic pressing is similar to that of hot-formed Ti-6Al-4V. The tensile RS found at the
surface of LPBF as-built samples decreased the fatigue life compared to the heat-treated samples. The modification of the microstructure (by heat treatment) did not affect the Fatigue performance in the elastic regime. This shows that in the absence of tensile RS, the manufacturing defects solely control the failure of LPBF components and densification has the strongest effect on the improvement of the mechanical performance.
In the present study, internal damage to an AlSi12CuMgNi alloy reinforced with planar random Al2O3 short fibres was investigated after compression testing. Due to the alloy composition, this composite contains a second reinforcement phase in the form of eutectic Si, which builds interpenetrated networks in the volume and increases the creep resistance and load-bearing capacity of the material. Materials with their fibre plane parallel and transversal to the load direction were characterized in order to investigate the dependence of load partition and damage on fibre plane orientation. In-situ compression testing during neutron diffraction measurements showed that internal damage is strongly influenced by the load partition between matrix and reinforcement. Moreover, micro-computed tomography was performed in the same material after ex-situ compression for damage analysis. In the case of a fibre plane perpendicular to the applied load, breakage and interconnected cracks appeared in a significantly higher volume fraction than with a fibre plane parallel to load.
Selective Laser Melting (SLM) technique allows to produce parts with complex geometry. Due to the rapid solidification and heat gradient during production, SLM results in presence of residual stress. The present study shows the influence of manufacturing parameters on surface residual stress of Ti-6Al-4V SLM parts. High tensile stresses in the front surface are found. Heat Treatment conditions relax residual stresses almost to zero. High scanning speed during manufacturing results in higher tensile stresses in the surface.
The reinforcement of concrete with polymer fibers provides resistance to crack formation. The orientation distribution of these fibers has a significant influence on the mechanical behavior of the material. To optimize material performance, micromechanical models that are capable of making accurate predictions of the mechanical behavior of composite materials are needed. These models must be calibrated using experimental results from microstructural characterization. For the fiber orientation distribution analysis in the present study, computed tomography (CT) data were used to evaluate the properties of a fiber-reinforced cement mortar. The results have indicated that the fibers in this material have highly anisotropic orientation characteristics and that there is a clear tendency for the polymer fibers to agglomerate during mixing and casting. The incorporation of this experimental data into micromechanical models will increase the accuracy of those models for material simulation and optimization.
Synchrotron X-ray diffraction is a powerful non-destructive technique for the analysis of the material stress-state. High cooling rates and heterogeneous temperature distributions during additive manufacturing lead to high residual stresses. These high residual stresses play a crucial role in the ability to achieve complex geometries with accuracy since they can promote distortion of parts during manufacturing. Furthermore, residual stresses are critical for the mechanical performance of parts in terms of durability and safety.
In the present study, Ti-6Al-4V bridge-like specimens were manufactured additively by selective laser melting (SLM) under different laser scanning speed conditions in order to compare the effect of process energy density on the residual stress state. Subsurface residual stress analysis was conducted by means of synchrotron X-ray diffraction in energy dispersive mode for three conditions: as-built on base plate, released from base plate, and after heat treatment on the base plate. The quantitative residual stress characterization shows a correlation with the qualitative bridge curvature method. Computed tomography (CT) was carried out to ensure that no stress relief took place owing to the presence of porosity. CT allows obtaining spatial and size pores distribution which helps in optimization of the SLM process.
High tensile residual stresses were found at the lateral surface for samples in the as-built conditions. We observed that higher laser energy density during fabrication leads to lower residual stresses. Samples in released condition showed redistribution of the stresses due to distortion.
Using non-optimum combination of manufacturing parameters in selective laser melting (SLM) may lead to reduction of quality of component: defects generation, distortion of geometry and even cracking. Usually, the optimization of parameters is performed by changing volumetric energy density (Ev) and selecting parameters giving low porosity values. However, not only low porosity but also stable microstructure and low residual stresses will help to achieve advanced mechanical behavior of the component.
In present work, we investigated cuboid-shaped Ti-6Al-4V samples produced with different manufacturing parameters. The parameters leading to the same Ev were considered as well as parameters which are not included in Ev. Residual stresses in subsurface region were investigated by synchrotron X-ray diffraction, which allows to penetrate around 100 µm from the surface therefore overcome the problem of high roughness of SLM components without additional sample preparation. Only tensile stresses were found along the building direction, that can play critical role especially during cyclic loading. The pore shape and spatial distribution obtained by computed tomography varied for samples produced with the same Ev. However, by using some process parameters it was possible to decrease residual stresses and obtain uniform α+β Ti microstructure and relatively low porosity. Additionally, it was found that not included in Ev (e.g., base plate position, focus distance) should be considered as additional manufacturing parameters during SLM process.
The reinforcement of concrete with polymer fibers provides resistance to crack formation. The orientation distribution of these fibers has a significant influence on the mechanical behavior of the material. To optimize material performance, micromechanical models that are capable of making accurate predictions of the mechanical behavior of composite materials are needed. These models must be calibrated using experimental results from microstructural characterization. For the fiber orientation distribution analysis in the present study, computed tomography (CT) data were used to evaluate the properties of a fiber-reinforced cement mortar. The results have indicated that the fibers in this material have highly anisotropic orientation characteristics and that there is a clear tendency for the polymer fibers to agglomerate during mixing and casting. The incorporation of this experimental data into micromechanical models will increase the accuracy of those models for material simulation and optimization.
Bei der additiven Fertigung können sich während des Prozesses aufgrund von hohen Aufheiz- und Abkühlraten Eigenspannungen ausbilden, die potentiell zu einem Verzug von Bauteilen führen und sich negativ auf das mechanische Verhalten auswirken. In dieser Studie wurden Ti-6Al-4V Proben durch Selektives Laserschmelzen mit verschiedenen Lasergeschwindigkeiten additiv gefertigt, um die Auswirkung der Laserenergiedichte auf den Eigenspannungszustand zu untersuchen. Die oberflächennahen Eigenspannungsanalysen wurden mittels energiedispersiver Synchrotronbeugung durchgeführt. Insgesamt wurden hohe Zugspannungen an den Seitenflächen der Proben gefunden. Es wurde festgestellt, dass je höher die Laserenergiedichte während der Fertigung ist, desto geringer fallen die Eigenspannungen aus. Eine nachträglich durchgeführte Wärmebehandlung führt zu einem vollständigen Abbau von Eigenspannungen.
Al-Si alloys produced by Laser Powder Bed Fusion (PBFLB) allow the fabrication of lightweight free-shape components. Due to the extremely heterogeneous cooling and heating, PBF-LB induces high magnitude residual stress (RS) and a fine Si microstructure. As the RS can be deleterious to the fatigue resistance of engineering components, great efforts are focused on understanding their evolution in as-built state (AB) and after post-process heat treatments (HT). RS in single edge notch bending (SENB) subjected to different HT are investigated (HT1: 1h at 265°C and HT2: 2h at 300°C).
The overview of the activity of Federal Institute for Material Research and Testing (BAM, Belin, Germany) in the field of additively manufacturing material characterization will be presented. The research of our group is focused on the 3D imaging of AM materials by means of X-ray Computed Tomography at the lab and at synchrotron, and the residual stress characterization by diffraction (nondestructive technique).
Hot Isostatic Pressing (HIP) is often introduced to tackle the porosity issue in additively manufactured (AM) materials. For instance, HIP post-processing is recommended to improve fatigue resistance of Laser powder bed fusion (PBF-LB) manufactured parts [1, 2]. Even though HIP cannot completely remove porosity, it significantly decreases the defect population and its average size below the critical threshold value leading to early crack initiation.
In the present study, in-situ investigation of HIP procedure of PBF-LB Ti-6Al-4V parts was carried out to gain further insights into the densification mechanism occurring during HIP. The in-situ observations at high pressure and high temperature are uniquely possible at the PSICHE beamline of the Soleil synchrotron (France), thanks to the Ultrafast Tomography on a Paris-Edinburgh Cell (UToPEC) and the combination of the fast phase-contrast tomography and energy-dispersive diffraction [3, 4]. A detailed methodology was developed to ensure that the correct pressure and temperature were maintained during the experiments.
The results allowed an estimation of the global dentification rate during HIP of PBF-LB Ti-Al-4V material, as well as a detailed quantitative characterization of the influence of pore size and shape on the densification process, thereby understanding the effectiveness of HIP process on different pore categories. After 20 mins, 75% of porosity can be considered as closed or has size below the resolution of the XCT reconstruction. We also observed that the smallest defects showed higher densification rate, while the defect shape did not have significant effect on such rate. The current development of in-situ HIP experiment allows experimental quantification and validation of the simulation work. Ultimately it paves the road to tailoring the HIP procedure for different materials depending on the porosity and microstructure.
The overview of the activity of Federal Institute for Material Research and Testing (BAM, Belin, Germany) in the field material characterization by X-ray imaging is presented. The principle of X-ray Computed Tomography (XCT) is explained. The multiple examples of application of quantitative analysis by XCT are reported, such as additive manufacturing, Li-ion battery, concrete research.
The focus of the presentation focus will be on 3D imaging by means of X-ray Computed Tomography (XCT) at the lab and at synchrotron, and the non-destructive residual stress (RS) characterization by diffraction of additively manufactured (AM) materials in BAM (Berlin, Germany). The manufacturing defects and high RS are inherent of AM techniques and affect structural integrity of the components. Using XCT the defects size and shape distribution as well as geometrical deviations can be characterized, allowing the further optimization of the manufacturing process. Diffraction-based RS analysis methods using neutron and synchrotron X-rays at large scale facilities offer the possibility to non-destructively spatially resolve both surface and bulk RS in complex components and track their changes following applied thermal or mechanical loads.
Ti-6Al-4V alloy is intensively used in the aerospace industry because of its high specific strength. However, the application of Laser Powder Bed Fusion (LPBF) Ti-6Al-4V alloy for structurally critical load-bearing components is limited. One of the main limiting factors affecting the structural integrity, are manufacturing defects. Additionally, the high cooling rates associated with LPBF process result in the formation of large residual stress (RS) with complex fields. Such RS can cause cracking and geometrical distortions of the part even right after production. Also, the microstructure of LPBF Ti-6Al-4V in the as-built condition is significantly different from that of the conventionally produced alloy. All these factors affect the mechanical behavior of the material. Therefore, to improve the material performance it is important to evaluate the individual effect of RS, defects, and microstructure on fatigue life. To this aim Ti-6Al-4V LPBF material in as-built condition and subjected to different post-processing, including two heat treatments (for stress relief and microstructural modification) and Hot Isostatic Pressing (HIP, for densification), were investigated.
Prior to Low Cycle Fatigue (LCF) tests at operating temperature (300°C), the microstructure (phases, crystallographic texture, and grain morphology), the mesostructure (defect shape and distribution), and subsurface RS on the LCF samples were investigated. It was found that the fatigue performance of HIPped samples is similar to that of conventionally produced Ti-6Al-4V. The tensile RS found at the surface of as-built samples decreased the fatigue life compared to heat-treated samples. Additionally, the modification of the microstructure (by heat treatment) did not affect the fatigue performance in the regime of mostly elastic strain. This shows that in the absence of tensile RS the manufacturing defects solely control the failure of LPBF components and densification has the strongest effect on the improvement of the mechanical performance.
Ti-6Al-4V alloy is intensively used in the aerospace industry because of its high specific strength. However, the application of Laser Powder Bed Fusion (LPBF) Ti-6Al-4V alloy for structurally critical load-bearing components is limited. One of the main limiting factors affecting the structural integrity, are manufacturing defects. Additionally, the high cooling rates associated with LPBF process result in the formation of large residual stress (RS) with complex fields. Such RS can cause cracking and geometrical distortions of the part even right after production. Also, the microstructure of LPBF Ti-6Al-4V in the as-built condition is significantly different from that of the conventionally produced alloy. All these factors affect the mechanical behavior of the material. Therefore, to improve the material performance it is important to evaluate the individual effect of RS, defects, and microstructure on fatigue life. To this aim Ti-6Al-4V LPBF material in as-built condition and subjected to different post-processing, including two heat treatments (for stress relief and microstructural modification) and Hot Isostatic Pressing (HIP, for densification), were investigated.
Prior to fatigue tests at elevated temperature, the microstructure, the mesostructure, and subsurface RS on the fatigue samples were investigated. It was found that the fatigue performance of HIPped samples is similar to that of conventionally produced Ti-6Al-4V. The tensile RS found at the surface of as-built samples decreased the fatigue life compared to heat-treated samples. Additionally, the modification of the microstructure (by heat treatment) did not affect the fatigue performance in the regime of mostly elastic strain. This shows that in the absence of tensile RS the manufacturing defects solely control the failure of LPBF components and densification has the strongest effect on the improvement of the mechanical performance.
The use of energetic materials as a main fuel in high temperature process
industries are not known to the scientific community as such. This paper
highlights some of the features and advantages of using organic peroxides
especially di-tert-butyl peroxide (DTBP) in high temperature process industries.
The feasibility of using DTBP as a main or supporting fuel in process industries
have also been justified with the help of Computational Fluid Dynamics (CFD)
simulations. For peroxides requirement of less fuel and air for the same amount
of heat flux has been shown. The resulted emission from the combustion of
DTBP is also discussed.
Experimental investigation and CFD simulation of organic peroxide pool fires (TBPB and TBPEH)
(2010)
Time averaged mass burning rate (m˙′′f ), flame length (H), temperature (T ), irradi- ance (E) and surface emissive power (SEP ) of TBPB (tert -butyl peroxybenzoate) and TBPEH (tert-butyl peroxy-2-ethylhexanoate) pool fires are measured for six pool di- ameters (d = 0.059 m, 0.107 m, 0.18 m, 0.5 m, 1 m and 3.4 m) at BAM in house and outside test facility. The measured heats of combustion (–Δhc) of TBPB and TBPEH are 30113 kJ/kg and 34455 kJ/kg and the specific heat capacities at constant pressure (cp) are 1.8 kJ/(kg K) and 2.1 kJ/(kg K) respectively. The measured m˙′′f of TBPB and TBPEH pool fires are in the range of 0.37 kg/(m2 s)≤ m˙ ′′ f ≤ 0.83 kg/(m2 s) and show little dependence on the pool diameter d, and are four to sixty times higher (for d = 1 m) than that of hydrocarbon pool fires. It is shown that the mass burning rates of the investigated organic peroxides can be represented as an exponential function of the self-accelerating decomposition temperature (SADT). Low SADT implies that the organic peroxide pool fires burn at a much higher m˙′′f than hydrocarbon pool fires. Fuel Froude numbers (Frf) of TBPB and TBPEH are 5 to 100 times (depending on d) higher than for hydrocarbon pool fires. Due to higher Frf the H of TBPB and TBPEH (measured with a S-VHS Videocamera) are found to be two times larger (d = 1 m) than corresponding pool fires of hydrocarbons. Heskestads flame length correlation predicts the Hd (d = 3.4 m) of TBPB and TBPEH pool fires much better than Thomas and Fay correlations. The measured time averaged flame temperatures T (d = 3.4 m) for TBPB and TBPEH pool fires are in the range of 1400 K ≤ T ≤ 1500 K and are 200 K to 300 K higher than for JP-4, kerosene and gasoline. The irradiances of the TBPB and TBPEH pool fires measured by radiometers are E (Δy/d = 0.3) = 45 kW/m2 and E = 98 kW/m2 which are two to ten times higher in comparison to the corresponding n-pentane, super gasoline and diesel pool fires. So the thermal safety distances for organic peroxide pool fires are larger by a factor four in comparison to the hydrocarbon pool fires. An infrared thermography system is used for the determination of SEP of TBPB and TBPEH pool fires. The values of surface emissive power for TBPB and TBPEH are SEP (d = 3.4 m) = 196 kW/m2 and SEP = 258 kW/m2 and thus the SEP are by a factor of approximately two higher than for hydrocarbon pool fires. A self-sustained pulsating Hd (’W’-Effect) is found in TBPB pool flames and is further analysed to explain the reason of occurance on the basis of chemical structure of the fuel and discontinuous heat flux back from flame to the liquid pool. CFD simulations of TBPB and TBPEH pool fires at d = 0.18 m, 0.5 m, 1 m, 3.4 m and 8 m are carried out using the Unsteady Reynolds Averaged Navier Stokes (URANS) equa- tions. The three-dimensional geometries have been discritized with unstructured hybrid grids, with the number of cells in the range of 1 million. Depending on the grid resolu- tion and the pool diameter time steps of 0.0001 s ≤ Δt ≤ 0.01 s for the CFD simulations are used. For solving the discritized equations a finite volume based implicit solver AN- SYS CFX has been used. For modelling the combustion, stoichiometric combustion for both peroxides are assumed. The temperature dependence of the reaction rate has been determined by the Arrhenius approach. For modelling the combustion eddy dissipation concept (EDC) model has been used. For turbulence buoyancy modified k- � and SAS (Scale Adaptive Simulation) turbulence models are used. For the thermal radiation and soot mass fraction discrete transfer radiation model and Magnusson soot model have been used. A new method is suggested for the prediction of mass burning rate (m˙′′f ) by CFD simula- tion. Both peroxide pool fires show approximately constant mass burning rate indepen- dent of d whereas m˙′′f of TBPEH are under predicted at the beginning but show relatively good agreement with measurements for large pool diameters (d = 1 m). In case of TBPB the CFD simulation over predicts the mass burning rate m˙′′f of small TBPB pool fires and shows a continuous decrease with d. CFD predicts the flame length H close to the measured data provided that the constants in Thomas equation are modified. The CFD predicted time averaged surface emission flame temperatures of TBPB and TBPEH pool fires (d = 3.4 m, 1437 K and 1542 K) are in good agreement with the measured time averaged flame temperatures. The CFD predicted SEP for TBPB and TBPEH pool fires (d = 3.4 m, 217 kW/m2 and 288 kW/m2) are also in agreement with the measured values. From the CFD predicted irradiance ECFD it is possible to determine the thermal safety distances from large pool fires of hydrocarbons and organic peroxides.
In present chapter, the potential usage of peroxy-fuels (usually known as organic peroxides) either in technically pure or in a blended form in engine combustion processes are explored. Although as additives (in small quantities <5% to conventional fuels, e.g., diesel, gasoline) peroxy-fuels are well known for many years their commercial applications as a main or primary fuel are not investigated in detail as such except a few. Their thermal instability and energy density demand great care during processing, which restricts their commercial exploitation. However, once the issues with safety are resolved they can be much more advantageously employed than conventional fuels. Some of these advantages are significant amount of fuel saving, reduction in amount of inducted air, or even the complete absence of air, i.e., anaerobic combustion, smaller volume of combustion (chamber), oxygenated fuel quality, and low emissions. An idea to develop the components of an engine operating solely on peroxy-fuels is also introduced. The engine concept is based on single and multiple injectors in a cylinder with special material coating to ensure a temperature-controlled processing.
The microstructure of most Seljuk and Ilkhanid stucco decorations consists of micrometer-sized crystals of gypsum. The stucco-masters of these periods (neither nowadays stucco-masters) were not able to directly control the properties of these tiny crystals with their hands or centimeter-sized tools. There are, however, traces of chaîne opératoire accumulated in the materialistic body of these pieces, some of which could be explored through an interdisciplinary approach. Such an investigation requires very careful in situ observation of the macrostructure, and scientific analyses of the material to discover part of the production process for each body of stucco. Furthermore, there are deterioration factors, some of which are not yet fully understood, and should be identified using modern analytical instruments. These damaging factors could easily affect the micro and macro structure of a stucco decoration, influencing our interpretation. The concept of chaîne opératoire reframes our questions about the production process and probable dating technique of Seljuk and Ilkhanid stuccoes, while analyses of labmade replicas and historic materials enhance our understanding and interpretation of these materials. Here we present the results of such a study for a large body of Seljuk and Ilkhanid stucco decorations at various sites in Iran, and present the potential of this approach as a new perspective in this field of research.
We show how historical gypsum plaster preparation methods affect the microstructure and the wettability properties of the final stucco materials. We reproduced a traditional Persian recipe (Gach-e Koshteh, ~14th century AD), which involves a continuous mechanical treatment during plaster hydration. These samples were compared with a laboratory-replicated historical recipe from Renaissance Italy (Gesso Sottile, ~15th century AD) and contemporary low-strength plaster. The Koshteh recipe induces the formation of gypsum platelets, which exhibit preferential orientation in the plaster bulk. In contrast,
the Italian and low-strength plasters comprise a typical needle-like morphology of gypsum crystals. The platelets in Koshteh expose the more hydrophilic {010} face of gypsum in a much more pronounced manner than needles. Consequently, the Iranian plaster displays enhanced wettability, enabling its direct use for water-based decoration purposes, or as a fine finishing thin layer, without the need of mixing it with a binder material.
Contrary, in Sottile, gypsum crystals are left to equilibrate in large excess of water, which promotes the growth of long needles at the expense of smaller crystals. Typically, such needles are several times longer than those found in a control regular plaster. For this
crystal habit, the total surface of hydrophilic faces is minimized. Consequently, such plaster layers tend to repel water, which can then be used, e.g., as a substrate for oilbased panel paintings. These findings highlight the development of advanced functional materials, by tuning their microtexture, already during the premodern era.
Es wird ausgeführt, dass die Wiederaufbereitung ausgedienter Brennelemente aus Druck- bzw. Siedewasserreaktor-Kernkraftwerken "schadlos durchführbar und wirtschaftlich vertretbar" ist und damit Vorrang hat vor einer Entsorgung ohne Wiederaufbereitung. In der Wiederaufbereitungsanlage Wackersdorf sind alle notwendigen Entsorgungsschritte von der Eingangslagerung bis zur endlagergerechten Behandlung von radioaktiven Abfällen zusammengefasst.
This work demonstrates that phase-segregated poly(ester urethane) (PEU) with switching segments of crystallizable poly(1,4-butylene adipate) (PBA) can be programmed to generate two separate stress recovery events upon heating under constant strain conditions. For programming, two elongations are applied at different temperatures, followed by unloading and cooling. During the adjacent heating, two-step stress recovery is triggered. The results indicate that the magnitude of the stress recovery signals corresponds to the recovery of the two deformation stresses in reverse order. As demonstrated by further experiments, twofold stress recovery can be detected as long as the elongation at higher temperature exceeds the strain level of the deformation at lower temperature. Another finding includes that varying the lower deformation temperature enables a control over the stress recovery temperature and thus the implementation of so-called “temperature-memory effects”. Moreover, exerting only one elongation during programming enables a heating-initiated one-step stress recovery close to the deformation temperature. Based on these findings, such polymers may offer new technological opportunities in the fields of active assembly when used as fastening elements and in functional clothing when utilized for compression stockings.
Formgedächtnispolymere werden durch thermomechanische Vorbehandlung, die Programmierung, in eine temporäre Form überführt. In die Ursprungsform kehren sie dann erst nach externer Stimulierung, durch Auslösen des Formgedächtniseffekts, wieder zurück. Um diesen Effekt zu optimieren, werden in dieser Arbeit thermomechanische Designoptionen analysiert und Stellschrauben der Programmierung diskutiert. Quantifiziert wird das Materialverhalten eines physikalisch vernetzten Polyurethans mit semikristalliner Polyester-Weichsegmentphase (PEU) in thermomechanischen Messungen, in denen das Polymer Dehnungen bis über 1000% fixiert.
Deformationen im breiten Schmelzübergangsbereich der Weichsegmentphase ermöglichen die präzise Kontrolle über die Temperaturen der Dehnungs- und Spannungsrückstellung, den bekannten Temperaturgedächtniseffekt (TGE). Erst durch eine neuartige Programmierung wird jedoch der Beginn der Rückstellung einstellbar. Für diesen Onset-TGE wird das PEU direkt nach dem Recken entlastet und danach unter die Kristallisationstemperatur abgekühlt. In situ Röntgenstreuung zeigt, dass durch den frühen Entlastungszeitpunkt nur der Teil der kristallinen Weichsegmentphase zur Fixierung beiträgt, der auch beim Recken kristallin ist. Die Kristallinität bietet daher eine Stellschraube, um das thermomechanische Verhalten zu veredeln. Über die Optimierungsparameter Reckrate, Temperaturhaltezeit und maximale Dehnung erzielt das PEU hohe Fixierbarkeiten und Rückstellspannungen, ohne die Rückstellung und den Onset-TGE zu beeinträchtigen. Durch die Erweiterung der Programmierung des Onset-TGEs hin zu einer zweiten Deformation und Entlastung innerhalb des Schmelzübergangs zeigt das PEU einen bisher nicht berichteten zweistufigen Spannungsanstieg während der Rückstellung. Ein Temperaturlimit für den Onset-TGE stellt die Peak-Schmelztemperatur aus der dynamischen Differenzkalorimetrie dar. Durch die verbleibende Kristallinität oberhalb dieser Temperatur führt die Deformation und Entlastung direkt zur thermoreversiblen Aktuation mit Dehnungsänderungen bis zu 28%.
Die Ergebnisse werden auf einen Miniaturisierungsansatz für schaltbare Informationsträger übertragen, mit denen eine maschinenlesbare Information von nichtlesbar nach lesbar geschaltet werden kann. In einer Machbarkeitsstudie wird der für Sensoranwendungen vielversprechende Onset-TGE genutzt, um die Lesbarkeit der Informationsträger bei einer vordefinierten Temperatur zu schalten. Das erweitert das potentielle Anwendungsfeld der Technologie vom Produkt- und Markenschutz zur Überwachung von Kühlketten.
Binary photoluminescent semiconductor nanocrystals (quantum dots, QDs) are one of the best studied fluorescent nanomaterials, and their unique optoelectronic properties paved the road to many applications in (bio)nanophotonics, optoelectronics, and photovoltaics. However, concerns related to their toxic constituents like cadmium or lead and the emerging interest in greener chemistry synthesis approaches hamper their future applicability. Interesting alternatives for some applications like biosensing or bioimaging are heavy-metal-free ternary QDs like AgInS2 (AIS), CuInS2 (CIS), and quaternary QDs such as AIS-ZnS (ZAIS). In this context, we explored the effect of ligand denticity on the organic-to-aqueous phase transfer of oleylamine-stabilized ZAIS QDs with the hydrophilic ligands mercaptopropionic acid (MPA), dihydrolipoic acid (DHLA), and 3-mercapto-2,2-bis(mercaptomethyl)propanoic acid (3MPA), bearing mono-, bi-, and trialkyl thiol groups. Spectroscopic studies of the resulting water-dispersible ZAIS QDs revealed a considerable influence of ligand denticity and ligand-to-QD ratio on the spectral position and width (FWHM; full width at half-maximum) of the photoluminescence (PL) bands, the PL quantum yields (PL QY), and the PL decay kinetics. Thiol capping and phase transfer resulted in a loss in PL by at least a factor of 2. The ligand-induced PL quenching observed particularly for ligands bearing two or three thiol groups was attributed to the facilitated formation of surface-bound disulfides. The best colloidal stability under high dilution conditions was observed for 3MPA.
In recent years, the fabrication of laser-generated surface structures on metals such as titanium surfaces have gained remarkable interests, being technologically relevant for applications in optics, medicine, fluid transport, tribology, and wetting of surfaces.
The morphology of these structures, and so their chemistry, is influenced by the different laser processing parameters such as the laser fluence, wavelength, pulse repetition rate, laser light polarization type and direction, angle of incidence, and the effective number of laser pulses per beam spot area.
However, the characterization of the different surface structures can be difficult because of constraints regarding the analytical information from both depth and the topographic artifacts which may limit the lateral and depth resolution of elemental distributions as well as their proper quantification. A promising technique to investigate these structures even at the nano-scale is Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS), a very surface sensitive technique that at the same time allows to perform depth-profiling, imaging and 3D-reconstruction of selected ion-sputter fragment distributions on the surface.
In this study we combine chemical analyses such as Energy Dispersive X-ray spectroscopy (EDX) and high-resolution scanning electron microscopy (SEM) analyses with ToF-SIMS to fully characterize the evolution of various types of laser-generated micro- and nanostructures formed on Ti and Ti alloys at different laser fluence levels, effective number of pulses and at different pulse repetition rates (1 – 400 kHz), following irradiation by near-infrared ultrashort laser pulses (925 fs, 1030 nm) in air environment or under argon gas flow.
We show how this combined surface analytical approach allows to evaluate alteration in the surface chemistry of the laser-generated surface structures depending on the laser processing parameters and the ambient environment.
Transparent conductive oxides such as indium tin oxide (ITO) are standards for thin film electrodes, providing a synergy of high optical transparency and electrical conductivity. In an electrolytic environment, the determination of an inert electrochemical potential window is crucial to maintain a stable material performance during device operation. We introduce operando ellipsometry, combining cyclic voltammetry (CV) with spectroscopic ellipsometry, as a versatile tool to monitor the evolution of both complete optical (i.e., complex refractive index) and electrical properties under wet electrochemical operational conditions. In particular, we trace the degradation of ITO electrodes caused by electrochemical reduction in a pH-neutral, water-based electrolyte environment during electrochemical cycling. With the onset of hydrogen evolution at negative bias voltages, indium and tin are irreversibly reduced to the metallic state, causing an advancing darkening, i.e., a gradual loss of transparency, with every CV cycle, while the conductivity is mostly conserved over multiple CV cycles. Post-operando analysis reveals the reductive (loss of oxygen) formation of metallic nanodroplets on the surface. The reductive disruption of the ITO electrode happens at the solid–liquid interface and proceeds gradually from the surface to the bottom of the layer, which is evidenced by cross-sectional transmission electron microscopy imaging and complemented by energy-dispersive X-ray spectroscopy mapping. As long as a continuous part of the ITO layer remains at the bottom, the conductivity is largely retained, allowing repeated CV cycling. We consider operando ellipsometry a sensitive and nondestructive tool to monitor early stage material and property changes, either by tracing failure points, controlling intentional processes, or for sensing purposes, making it suitable for various research fields involving solid–liquid interfaces and electrochemical activity.
The site of Schöningen (Germany), dated to ca. 300,000 years ago, yielded the earliest large-scale record of humanly-made wooden tools. These include wooden spears and shorter double-pointed sticks, discovered in association with herbivores that were hunted and butchered along a lakeshore. Wooden tools have not been systematically analysed to the same standard as other Palaeolithic technologies, such as lithic or bone tools. Our multianalytical study includes micro-CT scanning, 3-dimensional microscopy, and Fourier transform infrared spectroscopy, supporting a systematic technological and taphonomic analysis, thus setting a new standard for wooden tool analysis. In illustrating the biography of one of Schöningen’s double-pointed sticks, we demonstrate new human behaviours for this time period, including sophisticated woodworking techniques. The hominins selected a spruce branch which they then debarked and shaped into an aerodynamic and ergonomic tool. They likely seasoned the wood to avoid cracking and warping. After a long period of use, it was probably lost while hunting, and was then rapidly buried in mud. Taphonomic alterations include damage from trampling, fungal attack, root damage and compression. Through our detailed analysis we show that Middle Pleistocene humans had a rich awareness of raw material properties, and possessed sophisticated woodworking skills. Alongside new detailed morphometrics of the object, an ethnographic review supports a primary function as a throwing stick for hunting, indicating potential hunting strategies and social contexts including for communal hunts involving children. The Schöningen throwing sticks may have been used to strategically disadvantage larger ungulates, potentially from distances of up to 30 metres. They also demonstrate that the hominins were technologically capable of capturing smaller fast prey and avian fauna, a behaviour evidenced at contemporaneous Middle Pleistocene archaeological sites.
Zirconium vanadate (ZrV2O7) is a well-known negative thermal expansion (NTE) material that exhibits significant isotropic contraction over a broad temperature range (~150°C < T < 800°C). Therefore, it can be used to create composites with controllable expansion coefficients and prevent thermal stress, fatigue, cracking, and deformation at interfaces. We implement interdisciplinary research to analyze such material. We study the influence of the synthesis methods and their parameters on the sample's purity, crystallinity, and homogeneity. Moreover, we implement ab initio-based vibrational computations with partially treated anharmonicity in combination with experimental methods to follow temperature-induced structural changes and rationalize the negative thermal expansion in this material, including the influence of the local structure disorder.
Zirconium vanadate (ZrV2O7) is a well-known negative thermal expansion (NTE) material which exhibits significant isotropic contraction over a broad temperature range (~150°C < T < 800°C). The linear thermal expansion coefficient of ZrV2O7 is −7.1×10-6 K-. Therefore, it can be used to create composites with controllable expansion coefficients and prevent destruction by thermal shock.
Material characterization, leading to application, requires pure, homogenous samples of high crystallinity via a reliable synthesis route. While there is a selection of described syntheses in the literature, it still needs to be addressed which synthesis route leads to truly pure and homogenous samples. Here, we study the influence of the synthesis methods (solid-state, sol-gel, solvothermal) and their parameters on the sample's purity, crystallinity, and homogeneity. The reproducibility of results and data obtained with scanning electron microscopy (SEM), X-ray diffraction (XRD), differential scanning calorimetry, and thermogravimetric analysis (DSC/TGA) were analyzed extensively. The sol-gel method proves superior to the solid-state method and produces higher-quality samples over varying parameters. Sample purity also plays an important role in NTE micro and macro-scale characterizations that explain the impact of porosity versus structural changes.
Moreover, we implement ab-initio-based vibrational computations with partially treated anharmonicity (quasi-harmonic approximation, temperature-dependent effective harmonic potentials) in combination with experimental methods to follow and rationalize the negative thermal expansion in this material, including the influence of the local structure disorder, microstructure, and defects. Khosrovani et al. and Korthuis et al., in a series of diffraction experiments, attributed the thermal contraction of ZrV2O7 to the transverse thermal motion of oxygen atoms in V-O-V linkages. In addition to previous explanations, we hypothesize that local disorder develops in ZrV2O7 crystals during heating.
We are working on the experimental ZrV2O7 development and discuss difficulties one might face in the process as well as high-quality sample significance in further investigation. The obtained samples are currently used in the ongoing research of structure analysis and the negative thermal expansion mechanism.
Zirconium vanadate (ZrV2O7) is a well-known negative thermal expansion (NTE) material which exhibits significant isotropic contraction over a broad temperature range (~150°C < T < 800°C). The linear thermal expansion coefficient of ZrV2O7 is −7.1×10-6 K-. Therefore, it can be used to create composites with controllable expansion coefficients and prevent destruction by thermal shock.
Material characterization, leading to application, requires pure, homogenous samples of high crystallinity via a reliable synthesis route. While there is a selection of described syntheses in the literature, it still needs to be addressed which synthesis route leads to truly pure and homogenous samples. Here, we study the influence of the synthesis methods (solid-state, sol-gel, solvothermal) and their parameters on the sample's purity, crystallinity, and homogeneity. The reproducibility of results and data obtained with scanning electron microscopy (SEM), X-ray diffraction (XRD), differential scanning calorimetry, and thermogravimetric analysis (DSC/TGA) were analyzed extensively. The sol-gel method proves superior to the solid-state method and produces higher-quality samples over varying parameters. Sample purity also plays an important role in NTE micro and macro-scale characterizations that explain the impact of porosity versus structural changes.
Moreover, we implement ab-initio-based vibrational computations with partially treated anharmonicity (quasi-harmonic approximation, temperature-dependent effective harmonic potentials) in combination with experimental methods to follow and rationalize the negative thermal expansion in this material, including the influence of the local structure disorder, microstructure, and defects. Khosrovani et al. and Korthuis et al., in a series of diffraction experiments, attributed the thermal contraction of ZrV2O7 to the transverse thermal motion of oxygen atoms in V-O-V linkages. In addition to previous explanations, we hypothesize that local disorder develops in ZrV2O7 crystals during heating.
We are working on the experimental ZrV2O7 development and discuss difficulties one might face in the process as well as high-quality sample significance in further investigation. The obtained samples are currently used in the ongoing research of structure analysis and the negative thermal expansion mechanism.
Zirconium vanadate (ZrV2O7) is a well-known negative thermal expansion (NTE) material which exhibits significant isotropic contraction over a broad temperature range (~150°C < T < 800°C). The linear thermal expansion coefficient of ZrV2O7 is −7.1×10-6 K-1. Therefore, it can be used to create composites with controllable expansion coefficients and prevent destruction by thermal shock.
Material characterization, leading to application, requires pure, homogenous samples of high crystallinity via a reliable synthesis route. While there is a selection of described syntheses in the literature, it still needs to be addressed which synthesis route leads to truly pure and homogenous samples. Here, we study the influence of the synthesis methods (solid-state, sol-gel, solvothermal) and their parameters on the sample's purity, crystallinity, and homogeneity. The reproducibility of results and data obtained with scanning electron microscopy (SEM), X-ray diffraction (XRD), differential scanning calorimetry, and thermogravimetric analysis (DSC/TGA) were analyzed extensively. The sol-gel method proves superior to the solid-state method and produces higher-quality samples over varying parameters. Sample purity also plays an important role in NTE micro and macro-scale characterizations that explain the impact of porosity versus structural changes.
Moreover, we implement ab-initio-based vibrational computations with partially treated anharmonicity (quasi-harmonic approximation, temperature-dependent effective harmonic potentials) in combination with experimental methods to follow and rationalize the negative thermal expansion in this material, including the influence of the local structure disorder, microstructure, and defects. Khosrovani et al. and Korthuis et al., in a series of diffraction experiments, attributed the thermal contraction of ZrV2O7 to the transverse thermal motion of oxygen atoms in V-O-V linkages. In addition to previous explanations, we hypothesize that local disorder develops in ZrV2O7 crystals during heating.
We are working on the experimental ZrV2O7 development and discuss difficulties one might face in the process as well as high-quality sample significance in further investigation. The obtained samples are currently used in the ongoing research of structure analysis and the negative thermal expansion mechanism.
Zur Wirkungsweise und zum Einfluss unterschiedlicher Parameter beim Kathodischen Korrosionsschutz von Stahl in Beton wurden in der Vergangenheit bereits zahlreiche Untersuchungen durchgeführt. Über die Dauerhaftigkeit leitfähiger Beschichtung auf Karbonbasis als Fremdstromanode beim KKS von Stahlbeton liegen bislang keine umfassenden wissenschaftlichen Untersuchungen vor. Die in den einzelnen Arbeitspaketen (AP) erzielten Ergebnisse und gewonnenen Erkenntnisse tragen zum Verständnis über die Elektrodenreaktion der einzelnen Systeme bei. Die Frage der Dauerhaftigkeit konnte im Rahmen dieses Forschungsvorhabens nicht zur Gänze geklärt werden. Die Ergebnisse aus dem AP 1a liefern einen wesentlichen Beitrag zur Beantwortung der offenen Fragestellung hinsichtlich der vorherrschenden Elektrodenreaktion. In Verbindung mit dem Pourbaixdiagramm für Kohlenstoff lässt sich für die Beschichtungssysteme CBCC 1 und CBCC 2, nach 500 h andauernder Polarisation mit 10 mA/m² in ges. Calziumhydroxidlösung, die vorherrschende Elektrodenreaktion als Sauerstoffelektrode verifizieren. Im AP 1b wurde festgestellt, dass die an einem Praxisobjekt applizierten Systeme CBCC 1 und CBCC 2 in der Lage sind, die Schutzkriterien zu erfüllen. Die an diesem Objekt erforderlichen Schutzspannungen liegen jeweils zwischen 1 und 2 V. Die Anodenstromdichten betragen ca. 2,5 mA/m². Aufgrund der hohen Depolarisationsraten kann das Niveau der anliegenden Anodenstromdichten in Zukunft noch nach unten angepasst werden. Die Ergebnisse aus dem AP 1b und 1a sind erst zeitlich nach Festlegung der Prüfparameter für das AP 2a erzielt worden. Mit den ursprünglich veranschlagten Stromdichten von max. 40 mA/m² traten langfristig nachfolgende Problemstellungen auf: Bei der Stromeinleitung mittels Primärelektrode und Stromdichten größer gleich 20 mA/m² wurde festgestellt, dass die Versuche bei allen Systemen eine deutliche Entkopplung zwischen Primärelektrode und Beschichtung verursacht haben. Dies ist auf die hohen lokalen Stromdichten am Übergang Primärelektrode/leitfähige Beschichtung zurückzuführen. Eine Untersuchung der erforderlichen Kontaktfläche der Primärelektrode bezogen auf die effektive Stromdichte konnte nicht erfolgen. Weiterhin wurden die Haftzugwerte über die Dauer der Polarisation untersucht und mit unpolarisierten Proben verglichen. Eine Reduktion des Verbundes infolge Polarisation mit den angesetzten Stromdichten konnte verzeichnet werden. Es wurde jedoch auch festgestellt, dass mit zunehmenden Probenalter auch reduzierte Haftzugwerte an den geschliffenen und unpolarisierten Oberflächen der Referenzprobekörper ermittelt wurden. Die Grundlagen für die Simulation konnten in AP 3 anhand der gewonnen Ergebnisse erstellt werden und Feldverteilungen unter Berücksichtigung verschiedener Parameter berechnet werden. Eine auf den gewonnenen Erkenntnisse basierende Modellentwicklung für die Dauerhaftigkeitsprognose unter variierenden Randbedingungen, wie sie für AP 4 vorgesehen
war, konnte auf Basis der erzielten Ergebnisse nicht erfolgen. Dass die Beschichtungssysteme unter praxisüblichen Randbedingungen einsetzbar sind und bei dem Vergleich der Schutzspannung mit klassischen Systemaufbauten gleiche Schutzstromdichten erzielt werden, zeigt das AP 1b deutlich. Die zukünftigen Ergebnisse aus der Praxisanwendung (AP 1b) werden über die Projektlaufzeit hinaus ausgewertet und publiziert. Das Ziel des Vorhabens wurde teilweise erreicht.
Shrinkage measurements of miniaturized low temperature co-fired ceramics (LTCC) samples under load typically lead to collapsing of the samples, which hampers the characterization of shrinkage up to full densification. In this paper, a measurement setup is presented, which allows for in situ shrinkage measurements of practical, large LTCC panels during pressure-assisted sintering in a sintering press. The shrinkage behavior of two commercial LTCC systems (GreenTape 951 and Ceramtape GC) has been measured under loads of up to 1 MPa. No crushing of the specimens was observed and reproducible characterization of shrinkage up to full densification has been performed. Based on comparisons to thermomechanical analyzer measurements in this and other studies, it was found that the in situ approach is much better suited for shrinkage characterization of LTCC under load.
Reproducibility and accuracy of the method are discussed and practical as well as more academic applications are proposed.
A novel process to structure the surfaces of low temperature co-fired ceramics (LTCC) is presented. Lowered and raised structures are formed by hot-embossing with glass-like carbon molds during pressure-assisted sintering. Molding is driven by viscous flow of the LTCC glassy phase above the glass transition temperature. For accurate molding of embossments on the LTCC surface, proper filling of cavities in the glass-like carbon mold is necessary. Therefore, de-airing of the mold cavity has to be assured. Two strategies have been investigated: (i) hot-embossing at 850 °C after termination of LTCC shrinkage with de-airing through vent holes in the mold; and (ii) hot-embossing of open porous LTCC at 775 °C with dense molds, de-airing through pore channels in the LTCC, and subsequent densification by further heating to 850 °C. Circular embossments with 10 mm diameter were molded on a commercially available LTCC (Ceramtape GC, CeramTec GmbH, Marktredwitz, Germany). The sintered height was measured using optical profilometry. Image processing was used to evaluate porosity distributions in the sintered structures. The influence of embossing temperature on LTCC viscosity and mold filling behavior is discussed. Successful molding of 47 µm high raised grids and characters by hot embossing with 0.41 MPa at 775 °C and further heating to 850 °C under constant load is demonstrated. Thereby, the high potential of hot-embossing for precise structuring of LTCC surfaces is illustrated.
Structuring of LTCC Substrates by a Combination of Pressure-Assisted Sintering and Hot Embossing
(2015)
A novel technology for the structuring of low temperature co-fired ceramic (LTCC) surfaces is introduced. The commercial LTCC Ceramtape GC is shaped in a zero-shrinkage process by embossing a glass-like carbon mold into the softened LTCC during pressure-assisted sintering. Diverse raised and lowered structures including rings, grids, and characters were fabricated. It was found that de-airing of mold cavities is crucial for the molding of embossments. De-airing is possible through pore channels in the LTCC if embossing is performed at intermediate temperatures. The influence of LTCC viscosity on the mold filling behavior during the formation of raised structures is discussed. For accurate molding and proper densification of the LTCC, hot embossing with 0.41 MPa at 775 °C and subsequent heating under load to 850 °C is proposed. Embossing of precise, 40 µm deep circular cavities and 50 µm high raised bars and characters is demonstrated. Thereby, the high potential of the hot-embossing process for micro-patterning of LTCC is illustrated.
Structuring of LTCC substrates by a combination of pressure-assisted sintering and hot-embossing
(2015)
A novel technology for the structuring of LTCC surfaces is introduced. The material is shaped in a zero-shrinkage process by embossing a glassy carbon mold into the softened LTCC directly after termination of the shrinkage. Three commercially available LTCC compositions (Ceramtape GC, Heratape CT707, and DP951) were tested. Diverse raised and lowered structures including rings, grids, and characters were fabricated. Different material behavior was observed for the tested compositions. Promising results were achieved with Ceramtape GC. Embossing of precise, 40 µm deep circular cavities and 50 µm high raised characters is demonstrated. Processing of 100 × 100 mm² substrates is possible. DP951 showed very good moldability, but also unwanted material displacement due to evaporating lead. A high displacement capacity but uneven heights of embossed structures were observed on CT707 samples. SEM investigations proved the precise transfer of surface contours from the mold to the LTCC. Thereby, the high potential of the hot-embossing process for micro-patterning of LTCC is illustrated.
Niedrigsinternde Glas-Keramik-Komposite (LTCC, low temperature co-fired ceramics) werden erfolgreich als kompakte, mehrlagige Schaltungsträger in der Automobilindustrie und Hochfrequenztechnik eingesetzt. Dazu werden sie mit Verfahren der Folien- und Multilayertechnik verarbeitet und gemeinsam mit aufgedruckten Metallisierungen bei Temperaturen bis 900 °C co-gesintert. Besonders bei hohen Anforderungen an die Reproduzierbarkeit der Sinterschwindung hat sich das Sintern mit axialer Druckunterstützung etabliert, wodurch unter anderem die Schwindung in der Ebene der Einzelfolien unterdrückt werden kann. Ziel der vorliegenden Arbeit war es, die LTCC-Drucksintertechnologie unter zwei Gesichtspunkten weiterzuentwickeln:
• Erarbeitung eines einfachen und praktikablen Verfahrens zur Modellierung und Simulation des Verfahrens,
• prozessintegrierte Erzeugung maßgeschneiderter, speziell dünnfilmfähiger Oberflächenstrukturen.
Für die Simulation der Sinterung wurde das Modell der Mastersinterkurve ausgewählt. Die Eignung des Modells zur Beschreibung von LTCC-Werkstoffen wird zunächst ohne Druckunterstützung nachgewiesen. Dabei werden die Mastersinterkurven von frei gesinterten Pulverpresslingen und Folienlaminaten, deren Schwindung in der Ebene unterdrückt ist, quantitativ gegenübergestellt. Außerdem wird eine Methode vorgeschlagen und experimentell bestätigt, mit der die Schwindungsfehlpassung von Werkstoffkombinationen bei druckloser Co-Sinterung von berechnet werden kann. Die Modellierung der druckunterstützten Sinterung basiert auf thermomechanischen Analysen eines verbreitet angewendeten, kommerziellen LTCC-Werkstoffs (DuPont GreenTape DP951) im Druckbereich von 2 kPa bis 500 kPa. Die Auswertung der Messwerte und Entwicklung der Mastersinterkurven erfolgt unter Berücksichtigung der Kriechverformung des Werkstoffs unter Druck und wird durch grundlegende Untersuchungen zur für dieses Modell obligatorischen Bestimmung der Aktivierungsenergie ergänzt. Mit einer konstanten Aktivierungsenergie von 400 kJ/mol werden Mastersinterkurven für verschiedene Drücke aufgestellt und mit Anpassungsfunktionen modelliert. Die mit Hilfe der Anpassungsfunktionen simulierten Sinterkurven stimmen gut mit den Messungen überein. Das Modell wird als geeignet und praktikabel bewertet.
Die prozessintegrierte Erzeugung maßgeschneiderter Oberflächenstrukturen erfolgt über die im Drucksinterprozess eingesetzten Brennhilfsmittel. Zur Einstellung gewünschter Rautiefen auf den gesinterten Oberflächen werden Opferfolien aus Al2O3 mit unterschiedlichen Partikelgrößenverteilungen und eine Opferfolie aus hexagonalem BN vorgestellt, die über Rückstandsschichten auf der LTCC-Oberfläche die Oberflächenstruktur bestimmen. Der Zusammenhang von Opferfolieneigenschaften und Oberflächencharakteristika wird an verschiedenen LTCC-Werkstoffen beschrieben. Die Rauheit einer druckgesinterten LTCC-Oberfläche kann über die Partikelgröße der Opferfolien gezielt verändert werden. Zur Herstellung dünnfilmkompatibler, rückstandsfreier Oberflächen im Drucksinterprozess wird glasartiger Kohlenstoff als Brennhilfsmittel eingeführt. Damit wird eine Regelung des Sauerstoffpartialdrucks während des Brandes erforderlich. Eine vollständige thermische Entbinderung der Grünfolien ist aufgrund von Kohlenstoffrückständen auf den Partikeloberflächen erst oberhalb 500 °C möglich. Einflüsse der Prozessparameter Druck und Haltezeit auf die resultierende Oberflächenstruktur werden aufgeklärt und optimale Prozessfenster für die untersuchten Werkstoffe angegeben. Mit dem entwickelten Verfahren können zum ersten Mal verschiedene LTCC-Substrate mit dünnfilmfähigen Oberflächen nacharbeitsfrei durch Drucksintern hergestellt werden.
Die Ergebnisse zur Modellierung und Simulation leisten einen wertvollen Beitrag zur Einsparung von Energie, Zeit und Kosten bei der Gestaltung von Drucksinterprozessen. Die erarbeiteten Brennhilfsmittelkonzepte können ressourcenaufwändige Nacharbeit teilweise ersetzen und eröffnen durch die Dünnfilmeignung der Oberflächen neue Anwendungsgebiete der Drucksintertechnologie in der Sensor und Mikrosystemtechnik.
Aufgrund ihres spezifischen Eigenschaftsprofils sind keramische Federn attraktiv für Spezialanwendungen in Maschinenanlagen, Metrologie und Sensortechnik. Durch Hartbearbeitung keramischer Hohlzylinder können Spiralfedern mit rechteckigem Windungsquerschnitt präzise gefertigt werden. Dabei kann durch gezielte Auslegung der Federgeometrie die Federkonstante über mehrere Größenordnungen variiert werden. Der Vortrag gibt einen Überblick über den Herstellungsprozess, verschiedene Eigenschaften keramischer Federn und Anwendungsbeispiele.
Roughening of zirconia dental implants is a common clinical practice to improve ingrowth behavior. It depends on the manufacturer of the implant at which stage of the manufacturing process and by which method the surface is roughened. Systematic studies on this topic are rarely found in the literature. Therefore, the influence of surface treatment on the strength of a dental zirconia was investigated as part of a research project on the development of ceramic implants. The material under test was a commercial zirconia consisting of a Y-TZP matrix and Ce-TZP inclusions in the sintered state. This material is characterized by a slightly higher fracture toughness and slightly reduced strength compared to typical 3Y-TZP. Sets of samples were sandblasted in the white-fired or sintered condition. The ball-on-three-ball-strength of these samples was measured and compared to the strength of as-fired samples and polished samples. The complete study was performed two times for validation of the results. It is found that the average strength of TZP ceramics differs by almost 500 MPa depending on the surface treatment. Conventionally sintered specimens with as-fired surface exhibit a strength of 880 MPa. Sandblasting in the white fired state reduces the strength to 690 MPa. Both polishing and sandblasting in the sintered condition result in an increase in strength to about 1180 MPa. Comparative microstructural investigations, roughness measurements and X-ray phase analyses were carried out to determine the causes of these huge differences in strength. These findings may challenge the practice of white body surface treatment and give reason for further investigations on other commercial dental TZP materials.
Der Vortrag gibt einen Überblick über die Materialklasse Keramik, insbesondere Technische Keramik. Nach einem kurzen Überblick über typische Anwendungen und Werkstoffe wird die keramische Prozesskette erläutert. Am Beispiel von Festigkeit wird der für Keramik typische, enge Zusammenhang zwischen Technologie, Mikrostruktur und Eigenschaften herausgearbeitet. Daraus werden Anforderungen für eine erfolgreiche Digitalisierung abgeleitet.
Dielectric breakdown of insulators is a combined electrical, thermal, and mechanical failure. The exact breakdown mechanism in ceramics and the formulation of useful models are still subject of investigation. Recent studies highlighted that several experimental aspects of dielectric breakdown strength testing affect the test results, and thus impede the recognition of fundamental principles.
Excess field strength near the electrode can lead to premature breakdown in the insulating liquid. This would cause superficial damage to the test specimen and thus falsify the measurement results.
The field strength distribution is influenced by the ratio of permittivity of the sample and the surrounding insulating liquid. Premature breakdown depends on the breakdown strength of the liquid and the actual test voltage. The test voltage again depends on the specimen thickness.
To systematically investigate these relations, a numerical simulation study (FEM) of the electric field distribution in a typical testing rig with cylindrical electrodes was performed. The permittivity of the sample and the insulating liquid was parameterized, as well as the sample thickness. The electric field distribution was calculated for increasing test voltage. Field strength maxima are compared to experimental breakdown strength of typical insulating liquids and experimental breakdown locations on alumina. Strategies are discussed to adjust the insulation liquid and the sample thickness to reduce the influence of the testing setup on the dielectric breakdown strength results.
Advancements in pressure-assisted sintering technology for low temperature co-fired ceramics (LTCC)
(2016)
Steadily increasing demands on design and dimensional accuracy of ceramic multilayer modules, as well as the processing of new materials, require continuous improvements of manufacturing technology, especially thermal processes. The capabilities of pressure-assisted sintering (PAS) for the manufacturing of highly integrated low temperature co-fired ceramics (LTCC) multilayer have been considerably extended in the last years by procedural and device-related advancements. A lambda probe has been integrated in a sintering press prototype to monitor and control the process atmosphere. Thereby, the development of oxygen partial pressure during binder burnout of real modules can be observed. On the other hand, the oxygen partial pressure can be regulated during densification, for example to prevent diffusion of silver from circuit paths into the surrounding LTCC. Thin-film capable surfaces can be produced without post-processing by using setter plates made of glass-like carbon in an advanced PAS process under nitrogen. A newly developed advancement of this approach enables in-situ hot-embossing of LTCC during PAS by using structured glass-like carbon molds. The prototype press is further extended by a sensitive displacement transducer for monitoring the thickness shrinkage of real modules with an edge length of up to 8 inch.
Prägeverfahren bieten eine interessante Alternative zur Strukturierung keramischer Folien und Laminate. Im Gegensatz zur etablierten Stanz- oder Laserbearbeitung von Einzelfolien sind damit einerseits Strukturtiefen realisierbar, die nicht einem Vielfachen der Einzelfoliendicke entsprechen, andererseits können Strukturierungsgrade erzielt werden, bei denen perforierte Einzelfolien nicht mehr handhabbar sind. Heißprägen grüner Folien und Laminate erfolgt bei Temperaturen um 130 °C mit Metallstempeln. Die plastische Verformung erfolgt zeitabhängig. Dabei sind die Fließeigenschaften des polymeren Binders der Grünfolie maßgeblich für die Konturtreue der Prägung. Randeinzug und Gründichtegradienten um den Eindruck können zu Defekten im Sintergefüge führen. Je nach Sinterverfahren muss die Schwindung der geprägten Struktur berücksichtigt werden, eine Kombination dieses Verfahrens mit zero-shrinkage Techniken ist aber möglich. Sinterprägen stellt eine Erweiterung der Drucksintertechnologie für glaskeramische Komposite dar. Dabei wird ein Pressstempel aus glasartigem Kohlenstoff während des Brandes in die erweichte Glasphase des Komposits gedrückt. Die Abformung erfolgt durch viskosen Fluss der Glasphase. Mit Kenntnis des Dichte- und Viskositätsverlaufs des Werkstoffs kann das Verfahren so gestaltet werden, dass die Pressform konturtreu abgeformt wird. Mittels Sinterprägen lassen sich auch erhabene Strukturen realisieren, wobei diese häufig eine erhöhte Porosität aufweisen.