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Organisationseinheit der BAM
- 6 Materialchemie (229)
- 9 Komponentensicherheit (215)
- 7 Bauwerkssicherheit (164)
- 8 Zerstörungsfreie Prüfung (164)
- 5 Werkstofftechnik (161)
- 9.3 Schweißtechnische Fertigungsverfahren (118)
- 7.6 Korrosion und Korrosionsschutz (96)
- 8.5 Röntgenbildgebung (84)
- 6.6 Physik und chemische Analytik der Polymere (70)
- 1 Analytische Chemie; Referenzmaterialien (68)
Eingeladener Vortrag
- nein (443)
Der Vortrag gibt einen Überblick über das Chemikalienrecht, stellt die wichtigsten Regelungen sowie ihre Schnittstellen vor und gibt Informationen zu verfügbaren Hilfestellungen. Besprochen werden
• das UN-GHS (Globally Harmonized System of Classification and Labelling of Chemicals)
• REACH (EU-Verordnung zur Registrierung, Bewertung, Zulassung und Beschränkung chemischer Stoffe)
• CLP (EU-Verordnung über die Einstufung, Kennzeichnung und Verpackung von Stoffen und Gemischen)
• Gefahrstoffverordnung
The physical and chemical effects of diesel and biodiesel fuels on two high-density polyethylene (PE-HD) types were investigated. Both semi-crystalline PE-HD are common thermoplastic materials for container and storage tank applications. Biodiesel, a composition of unsaturated fatty acid esters from renewable resources, was chosen as it is regarded a possible green alternative to fossil fuels. The study aims at identifying significant differences between biodiesel and conventional diesel fuels based on the differences in the chemical nature of the two. The physical effects of the fuels on the polymer at first comprises the sorption behavior, i.e. kinetics and final equilibrium concentration. Not only are both fuels absorbed by the amorphous phase of the semi-crystalline PE-HD, they also induce a plasticization effect that modifies the molecular mobility and therefore also the characteristic yielding properties, manifest in the obtained stress-strain curves. The chemical effects related to degradation phenomena is investigated by a long-term storage scenario using partially immersed tensile test specimens in diesel and biodiesel. We were able to confirm the proposed co-oxidation mechanism by Richaud et al. for polyethylene-unsaturated penetrant systems on a larger scale based on practical tensile tests. One of the investigated polyethylene grades subjected to tensile drawing showed a significant loss of plastic deformation and the onset of premature failure after 150 days of storage in biodiesel. Further biodiesel storage showed a systematically reduced elongation at break before necking. None of these effects were observed in diesel. Oxidation of fuels and polymer after progressing storage times were analyzed by the evolution of carbonyl species in FT-IR/ATR spectroscopy.
Chemical composition of the welding seam and HAZ has significant effect on weld quality.
Current inspection methods for weld seams measure and investigate post factum and cannot prevent weld defects. Element burn-off may significantly affect solidification leading to embrittlement or cracking. Control of weld chemical compositions insures a controlled solidification and resistance to related weld defects. “Industry 4.0” is the current trend of automation and data exchange in manufacturing technologies. With this trend “intelligent” welding machines will be developed. LIBS can provide significantly important online data for such systems.
Relative and Absolute Methods for Measuring Photoluminescence Quantum Yields of UV/vis/NIR Emitters
(2019)
One of the key spectroscopic performance parameters of molecular and particulate emitters is the photoluminescence quantum yield (PL QY) that provides a direct measure for the number of emitted per absorbed photons. This triggered the interest in methods suitable for measuring this property for emitters in various environments in the UV/vis/NIR and above 1000 nm as well as on the ensemble and single emitter level. Moreover, for nonlinear emitters like lanthanide-based upconversion nanocrystals methods including instrumentation for power density-dependent PL QY studies are required.
An overview of the research activities in Division Biophotonics of BAM is given and suitable relative and absolute methods for the deter-mination of PL QY of organic dyes and different types of application-relevant nanomaterials in dispersion and in the solid state are presen-ted. This covers also the design and calibration of integrating sphere setups, achievable uncertainties, and candidates for PL QY reference materials.
Mechanochemistry is a fast and efficient method applicable for the synthesis of new organic, metal-organic, and inorganic compounds. The direct monitoring of milling reactions is still challenging. The underlying reaction mechanisms remain often unclear. In the last years, have established a tandem in situ approach for investigating mechanochemical reactions using time-resolved in situ XRD coupled with Raman spectroscopy. Here, we present an in situ coupling of synchrotron XRD, Raman spectroscopy, and thermography allowing the observation of mechanochemical reactions in real time. Information on the crystalline, molecular, and temperature state of the materials during grinding could be collected. The chemical composition of the reaction mixture was found to be directly correlated with changes in the temperature profile of the reaction. Furthermore, the presented setup allows the detection of crystalline, amorphous, eutectic as well as liquid intermediates. The resulting deeper kinetic and thermodynamic understanding of milling processes is the key for future optimization of mechanochemical syntheses.
The stability of the low thermal conductivity in Fe2TiO5 pseudobrookite ceramics has been studied. An increase in thermal diffusivity is observed after only three cycles of measurement. X-ray refraction shows an increase in the mean value of specific surface after the thermal diffusivity measurements. By using scanning electron microscopy and high‐angle annular dark‐field scanning transmission electron microscope equipped with energy dispersive X-ray spectroscopy, we observe a segregation of Ca- and F-rich nanocrystals at grain boundaries after three cycles of thermal diffusivity measurement. Therefore, impurities seem to be more efficient to scatter phonons as point defects in the pseudobrookite lattice rather than as nanocrystals at pseudobrookite grain boundaries. This emphasizes the importance of precursor purity and the influence of redistribution of impurities on thermoelectric properties: stability of micro-/nano-structures is a key point, and repeated thermoelectric measurements may allow detecting such metastable micro- /nano-structures and producing stable and reliable data.
Selection and study of alkoxysilanes as loading in submicrocapsules for self-lubricating coatings
(2019)
The possibility and conditions for the formation of nano- or submicrocapsules loaded with hydrophobic active ingredients (alkoxysilanes) into the matrix of coatings with self-lubricating effect are considered. The optimal composition of the alkoxysilane submicrocapsules, and their physicochemical properties were determined. The longer the radical chain length is, the lower is the rate of hydrolysis, and, accordingly, the more stable is the formed emulsion. The methods of laser correlation spectroscopy in measuring the size and zeta potentials of the submicrocapsules with different loads of the active agent allowed to determine the optimal ratios of the active ingredients. The optimal concentration of the active agent is between 4 and 9%. Based on contact angle studies, octadecyltrimethoxysilane was selected as optimum compound. The introduction of 4 wt% of octadecyltrimethoxysilane reduces the friction coefficient of coatings by 20–30% under vibrating motion and by 15–20% under continuous motion. The data obtained can also be useful for the encapsulation of other hydrophobic active agents and for various other purposes, for example, for the introduction of biocidal agents.
Carbon dots have attracted much attention due to their unique optical, chemical and electronic properties enabling a wide range of applications. The properties of carbon dots can be effectively adjusted through modifying their chemical composition. However, a major challenge remains in understanding the core and surface contributions to optical and electronic transitions. Here, three blue luminescent carbon dots with carboxyl, amino and hydroxyl groups were comprehensively characterized by UV-vis absorption and emission spectroscopy, synchrotron-based X-ray spectroscopy, and infrared spectroscopy. The influence of the surface functionality on their fluorescence was probed by pH-dependent photoluminescence measurements. Moreover, the hydrogen bonding interactions between water and the surface groups of carbon dots were characterized by infrared spectroscopy. Our results show that both core and surface electronic states of blue luminescent carbon dots contribute to electronic acceptor levels while the chemical nature of the surface groups determines the hydrogen bonding behavior of the carbon dots. This comprehensive spectroscopic study demonstrates that the surface chemistry has a profound influence on the electronic configuration and surface–water interaction of carbon dots, thus affecting their photoluminescence properties.
Photon upconversion nanomaterials have a wide range of applications, including biosensing and deep-tissue imaging. Their typically very weak and narrow absorption bands together with their size dependent luminescence efficiency can limit their application potential. This has been addressed by increasingly sophisticated core-shell particle architectures including the sensitization with organic dyes that strongly absorb in the near infrared (NIR). In this work, we present a simple water-dispersible micellar system that features energy transfer from the novel NIR excitable dye, 1859 SL with a high molar absorption coefficient and a moderate fluorescence quantum yield to oleate-capped NaYF4:20%Yb(III), 2%Er(III) upconversion nanoparticles (UCNP) upon 808 nm excitation. The micelles were formed using the surfactants Pluronic F-127 and Tween 80 to produce a hydrophilic dye-UCNP system. Successful energy transfer from the dye to the UCNP could be confirmed by emission measurements that revealed the occurrence of upconversion emission upon excitation at 808 nm and an enhancement of the green Er(III) emission compared to direct Er(III) excitation at 808 nm.
Die Bewertung der Werkstoffbeständigkeit ist von großer Bedeutung bei Änderung der Zusammensetzung der Kraftstoffe und des Heizöls, insbesondere die Frage nach der Beständigkeit der Dichtungswerkstoffe bei Zusätzen von Bioethanol und Biodiesel (Rapsölfettsäuremethylester).
Vorhergehende Untersuchungen (Messungen der Veränderungen der Masse, der Zugeigenschaften und der Härte) bezogen sich auf die Bewertung der Beständigkeit häufig verwendeter Dichtungswerkstoffe wie FKM, FVMQ, VMQ, EPDM, CR, CSM, IIR, PA, NBR und PUR in Kraftstoffen und Heizöl mit 10 % Biodiesel (nicht gealtert und bis zu 5 Jahre gealtert) unter statischen Bedingungen.
Ziel der Untersuchungen war die Bewertung der Beständigkeit von Fluorkautschuk unter verpressten Bedingungen in Analogie zu den Einsatzbedingungen in der Praxis. Die Masse und der Druckverformungsrest von Prüfkörpern aus FKM wurden vor und nach der Auslagerung über einen Zeitraum von 3, 7, 14, 28, 56 und 90 Tagen in E10 (Kraftstoff mit max. 10 % Ethanol), E85 (Kraftstoff mit 85 % Ethanol), Biodiesel (Rapsölfettsäuremethylester), Super (Kraftstoff mit max. 5 % Ethanol), Dieselkraftstoff mit max. 5 % Biodiesel, Super Plus (Kraftstoff ohne Ethanolzusatz) und Heizöl mit 10 % Biodiesel (B10) bei 40 °C gemäß ISO 815-1 bestimmt. Die Druckverformungsrestprüfung zählt neben der Messung der Härte, der Dichte und der Zugeigenschaften zu den wichtigsten Grundprüfverfahren der Elastomerindustrie. Nach Ende der Auslagerung in den Kraftstoffen und der Aufhebung der Verpressung wur-de der Druckverformungsrest der Prüfkörper in regelmäßigen Zeitabständen bis zu einer Rücktrocknung > 90 Tage bestimmt. Zum Vergleich wurden Prüfkörper aus FKM ohne Kraftstoff oder Heizöl unter Verpressung bei 40 °C ausgelagert.
Die Masseänderung der Prüfkörper aus FKM betrug nach 90 Tagen Auslagerung in E10 9 %, in Super 8 %, in E85 4% und 0,6 % in Biodiesel. Die Erhöhung der Masse und die damit verbundene Quellung der Prüfkörper in E10 und Super mit 5 – 10% Ethanolzusatz hatte einen Einfluss auf den Druckverformungsrest, der sprunghaften Veränderungen unterlag im Vergleich zu den Werten nach Auslagerung in Biodiesel, Dieselkraftstoff und Heizöl B10 bei 40 °C. Zum Vergleich, unter statischen Bedingungen verringerte sich die Zugfestigkeit der Prüfkörper aus FKM nach Auslagerung in E10 bei 40 °C um 31 % und die Reißdehnung um 18 %.
The shape of the weld pool in laser beam welding plays a major role to understand the dynamics of the melt and its solidification behavior. The aim of the present work was its experimental and numerical investigation. To visualize the geometry of the melt pool in the longitudinal section a butt joint configuration of 15 mm thick structural steel and transparent quartz glass was used. The weld pool shape was recorded by means of a high-speed video camera and two thermal imaging MWIR and VIS cameras. The observations show that the dimensions of the weld pool vary depending on the depth. The regions close to the surface form a teardrop shaped weld pool. A bulge-region and its temporal evolution were observed approximately in the middle of the depth of the weld pool. Additionally, a transient numerical simulation was performed until reaching a steady state to obtain the weld pool shape and to understand the formation mechanism of the observed bulging phenomena. A fixed keyhole with an experimentally obtained shape was used to represent the full-penetration laser beam welding process. The model considers the local temperature field, the effects of phase transition, thermo-capillary convection, natural convection and temperature-dependent material properties up to evaporation temperature. It was found that the Marangoni convection and the movement of the laser heat source are the dominant factors for the formation of the bulging-region. Good correlation between the numerically calculated and the experimentally observed weld bead shapes and the time-temperature curves on the upper and bottom surface were found.
In this paper we report on the characterization by X-ray computed tomography of calcium phosphate (CaP) and polycaprolactone (PCL) coatings on Ti-6Al-4V alloy scaffolds used as a material for medical implants. The cylindrical scaffold has greater porosity of the inner part than the external part, thus, mimicking trabecular and cortical bone, respectively. The prismatic scaffolds have uniform porosity. Surface of the scaffolds was modified with calcium phosphate (CaP) and polycaprolactone (PCL) by dip-coating to improve biocompatibility and mechanical properties. Computed tomography performed with X-ray and synchrotron radiation revealed the defects of structure and morphology of CaP and PCL coatings showing small platelet-like and spider-web-like structures, respectively.
Bestrebungen zum Leichtbau sowie höhere Anforderungen an das ertragbare Lastkollektiv führen in der Auslegung von Schweißkonstruktionen zunehmend zum Einsatz hochfester Feinkornbaustähle. Ohne Anwendung kostenintensiver Nachbehandlungsverfahren ist die Lebensdauer hochfester Schweißverbindungen unter wechselnder zyklischer Beanspruchung jedoch limitiert. Neben der geometrischen Kerbe sind schweißbedingte Gefügeveränderungen und die Höhe und die Verteilung von Schweißeigenspannungen für die Eigenschaften von Schweißverbindungen von erheblicher Bedeutung. Sogenannte LTT-Zusatzwerkstoffe bieten eine äußerst lukrative Möglichkeit, die resultierenden Schweißeigenspannungen bereits während des Schweißens zu adaptieren. Durch die gezielte Ausnutzung der mit der martensitischen Phasenumwandlung verbundenen Volumenausdehnung können bei hinreichend niedriger Umwandlungstemperatur Druck oder niedrige Zugeigenspannungen induziert werden. Bisherige Untersuchungen konzentrieren sich vorrangig auf die Entwicklung von LTT-Legierungskonzepten sowie dem Nachweis von Druckeigenspannungen, bieten jedoch nur wenige Erkenntnisse zum Einfluss der Wärmeführung, vor allem der Zwischenlagentemperatur, oder der Schrumpfbehinderung auf die Beanspruchung von LTT- Mehrlagenschweißverbindungen unter realitätsnahen Fertigungsbedingungen.
Die Interaktion zwischen der martensitischen Phasenumwandlung und den thermischen bzw. den mechanischen Einflussfaktoren auf die Schweißeigenspannungen wurde einleitend durch elementare Schweißversuche analysiert. Mit Hilfe des Temperaturgradienten wurde der Einfluss der behinderten thermischen Schrumpfung auf den Eigenspannungszustand in LTT-Schweißverbindungen erstmalig richtungsabhängig verstanden. Unter der Vorlage eines hohen Einspanngrades wurden Druckspannungen bevorzugt aufgebaut, wenn der Temperaturgradient während der Phasenumwandlung nur schwach ausgeprägt war. Dabei durchgeführte In-situ-Beugungsexperimente haben gezeigt, dass der Einspanngrad nur in Zusammenhang mit der richtungsabhängig vorliegenden behinderten thermischen Schrumpfung zu betrachten ist, um die Beanspruchung einer Schweißverbindung unter konstruktiver Schrumpfbehinderung bauteilübergreifend bewerten zu können.
Anschließend wurden Mehrlagenschweißversuche unter freier Schrumpfung sowie in einer speziellen Prüfanlage unter konstruktiver Schrumpfbehinderung und realistischen Fertigungsbedingungen durchgeführt. Es gelang der Nachweis, dass durch die Verwendung von LTT-Legierungen das Reaktionsmoment Mx gegenüber einer konventionellen Schweißverbindung unabhängig von der Zwischenlagentemperatur reduziert wird. Dennoch nimmt die Reaktionsspannung σ_total mit zunehmender Zwischenlagentemperatur zu. Mit Hilfe des Temperaturgradienten wurde der Einfluss der behinderten thermischen Schrumpfung auf die lokale und die globale Beanspruchung der untersuchten Schweißverbindungen interpretiert. Unabhängig von der genutzten Zwischenlagentemperatur lag für die LTT-Stumpfstoßverbindungen vor allem in Longitudinalrichtung nur eine geringe Schrumpfbehinderung während der martensitischen Phasenumwandlung vor. Dadurch wurden während der Abkühlung vor allem im Volumen Druckspannungen in Longitudinalrichtung aufgebaut. Der Eigenspannungszustand von LTT-Verbindungen wird darüber hinaus durch inhomogene Phasenumwandlung der Schweißnaht infolge von Konzentrationsunterschieden verschiedener Elemente im Schweißgut bestimmt.
Das 1986 erstmalig erschienene und bewährte Fachbuch wurde, nachdem die 2014 herausgegebene 6. Auflage vergriffen war, auf den neuesten Stand gebracht und im Rahmen der,,Kontakt & Studium“‐Serie der Technischen Akademie Esslingen als Band 686 neu aufgelegt, um die ungebrochene Nachfrage zu befriedigen. Dabei wurden die nach der vorherigen Ausgabe geänderten Normen sowie einige Abbildungen und die Liste der Dissertationen aktualisiert.
Wie schon in den vorherigen Ausgaben bietet dieses Buch Studierenden der technischen Fach‐ und Hochschulen eine gute Unterstützung und ist insbesondere für die in der Industrie tätigen Techniker, Konstrukteure und Ingenieure zu empfehlen. Die aktualisierte Bibliographie der zum Thema einschlägigen Dissertationsschriften am Ende des Werkes bietet auch einen hohen Nutzen für den wissenschaftlichen Gebrauch.
Modelling of environmentally assisted material degradation in the crack phase-field framework
(2019)
The simulation of crack propagation was conducted with a diffusive crack model in a variational framework. Moreover, the physically sound introduction of mass transport and coupling mechanisms due to environmentally assisted effects could be realised in this framework. The objective consists of the application of the phase-field Approach towards the simulation of environmentally assisted material degradation with the advantage of a non-required predefined crack path and a mesh-independent non-local formulation that facilitates the damage evolution with respect to material softening. The sharp crack is regularised by the introduction of a phase-field order parameter leading to a diffusive crack formulation.
Besides the equations originating from the linear momentum balance an additional evolution equation for the crack phase-field is introduced. Furthermore, mass transport is simulated by a Diffusion equation. The description delivered by the variational phase-field framework is able to simulate crack propagation according to published numerical test cases.
Additionally, the calculation of stress intensity factors is possible as well as crack resistance curves that describe stable crack propagation.
Water migration in one-side heated concrete: 4D in-situ CT monitoring of the moisture-clog-effect
(2019)
Explosive spalling due to fire exposure in concrete structures can lead severe damage and, in the worst case, to premature component failure. For this reason, an in situ investigation of water Migration in concrete due to surface heating was undertaken.
During these experiments, a miniaturized concrete specimen within a confining and insulating double-hull was subjected to surface heating during simultaneous X-ray computed tomography (CT) scanning. Through the use of subtraction-based Image analysis techniques, it was possible to observe and quantify not only drying within areas of the concrete matrix close to the heated surface, but also the migration of moisture to both pore and matrix regions deeper within the specimen. It was also discovered that the correction of CT images for specimen deformation using DVC and variable detector performance using calibrated image filters significantly improved the quality of the results. This clearly demonstrates the potential of X-ray CT for evaluation of other rapid-density-change phenomena in concrete and other building materials.
The paper focuses on the reformulation of classic Maxwell's (1873) homogenization method for calculation of the residual stresses in matrix composites. For this goal, we equate the far fields produced by a set of inhomogeneities subjected to known eigenstrains and by a fictitious domain with unknown eigenstrain. The effect of interaction between the inhomogeneities is reduced to the calculation of the additional field acting on an inhomogeneity due to the eigenstrains in its neighbors. An explicit formula for residual stresses is derived for the general case of a multiphase composite. The method is illustrated by several examples. The results are compared with available experimental data as well as with predictions provided by the non-interaction approximation (Eshelby solution). It is shown that accounting for interaction can explain many experimentally observed phenomena and is required for adequate quantitative analytical modeling of the residual stresses in matrix composites.
Three-dimensional (3D) γ-MnO2@ZnFe2O4/reduced graphene oxide (rGO) nanohybrids were synthesized using a one-pot hydrothermal self-assembly method. The morphology and properties of the nanohybrids were investigated.
The synergistic interactions among γ-MnO2, ZnFe2O4, and rGO resulted in 3D nanoflakes distributed uniformly in the rGO structure with a thickness of approximately 2–5 nm, leading to a high surface area. The nanohybrid containing 10 wt. % rGO exhibited superior catalytic activities for phenol degradation through the activation of peroxymonosulfate (PMS) to generate active sulfate radicals (SO4 •–). Typically, 50 mL of a 20 ppm phenol solution was degraded completely and 85% of the carbon content had been mineralized in 30 min at 25 °C using 10 mg of the nanohybrid. The nanohybrid could be recovered easily using a magnet and reused, maintaining high stability during catalytic oxidation. The 3D γ-MnO2@ZnFe2O4/rGO nanohybrid catalyst could be applied to the removal of hard-to-degrade waste materials owing to its high efficiency and excellent reusability.
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.
The structural and thermoelectric properties of Na- and Ag-substituted CoO dense ceramics have been investigated. X-ray diffraction shows that pure phase and Ag/CoO composites have been obtained for Na-doped and Ag-doped CoO, respectively. Raman spectroscopy shows an effect of Na dopants on the lattice disorder of CoO. The chemical composition, element distribution, and valence states of the samples have been characterized by Auger electron microscopy and X-ray photoelectron spectroscopy. Substitution of Co by 5 at. % Na enhances the power factor to 250 μWm−1 K-2 at 1000 K, similar to that of Ca3Co4O9. The corresponding thermal conductivity is also reduced to 3.55 W.m−1 K−1 at 1000 K. Consequently, Co0.95Na0.05O exhibits the best thermoelectric figure of merit (ZT), which is 0.07 at 1000 K. On the other hand, the substitution of Ag into CoO leads to the formation of CoO/Ag composites and deteriorates ZT values.
AISI D2 is one of the most applied cold-working tool steel for deep drawing operations, due to the materials good toughness and high wear resistance. However, since the lubricant-free deep drawing as well as the processing of high strength and ultra-high strength steel sheets remaining ongoing trends in the automotive industry, the tool surfaces need to be improved regarding their friction and wear behavior. For this purpose elevated micro textures can be applied. Since protruded micro features are predominantly affected by wear, a structuring process enabling the formation of suitable textures with high wear resistance is needed.
In this paper surface texturing at microscale was conducted by laser implantation. This technique allows the fabrication of highly wear resistant, separated and elevated features (implants) on steel surfaces via a discontinuous dispersing of ceramic particles by pulsed laser radiation. The aim of this study was to investigate the techniques potential for the creation of wear resistant elevated micro features on AISI D2 tool steel surfaces by the application of TiB2 particles. The laser parameters (pulse power and length) were varied and a comparative material analysis on AISI D2 laser remelted spots and TiB2 localized dispersed zones was examined. High-speed camera recordings allowed the description of the particle insertion mechanism from pre-coatings during laser processing. Mechanical properties were analyzed by (micro-) hardness measurements at top and cross sections. The microstructure was investigated by optical microscopy, scanning electron microscopy (SEM), energy dispersive Xray
spectroscopy (EDX) and X-ray diffraction (XRD). The implants geometrical properties (diameter, height, depth) were investigated by white light interferometry and optical microscopy. The experiments reveal that a pulsed laser remelting of AISI D2 leads to a significant hardness drop due to high retained austenite (γR) contents. Contrary, a localized dispersing of TiB2 particles leads to defect free dome- or ring-shaped elevated features with hardness values up to 1800 HV1. The high hardness values result from the dispersed TiB2 particles and an in-situ precipitation of new hard particle phases, which lead to a reduction of the γR content within the matrix.
The elemental dissolution of Cu-Zn alloys was investigated as a function of Zn content ranging from 0 to 45 wt%. Atomic emission spectroelectrochemistry (AESEC) was utilized to directly monitor Cu2+ and Zn2+ release and oxide growth as function of time during potentiodynamic experiments. It was determined that Cu dissolution undergoes a simultaneous mechanism of Cu2O formation and Cu2+ release. The addition of Zn in Cu-Zn alloy does not measurably change the dissolution mechanism of Cu2+ and the rate of aqueous Cu2+ was only dependent on the potential. Zn dissolution was however blocked by the formation of a Cu(0) film which shifted the Zn dissolution in the anodic direction.