Fast lateral hydrogen diffusion in magnesium-hydride films on sapphire substrates studied by electrochemical hydrogenography

Hydrogen diffusion in thin magnesium films in lateral film direction is studied by stepwise electrochemical loading via the change in optical light transmission (‘electrochemical hydrogenography’) during the dihydride formation. During the first loading step, the dihydride front propagation kinetics allows determining the lateral hydrogen diffusion coefficient in the film, by applying an analytical model and, alternatively, by comparison with finite-element simulations. Subsequent loading steps show a time lag behavior in the dihydride front propagation. Therefore, they can be regarded as permeation experiments. These subsequent loading steps can be explained by hydrogen diffusion along grain boundaries and by taking the Gaussian shape of the hydrogen site energy distribution in the grain boundaries into account. In average, an effective hydrogen diffusion coefficient of $3_{?2}^{+12}?{10}^{?12}\raisebox{1ex}{${\text{m}}^2$}\!\left/ \!\raisebox{-1ex}{$\text{s}$}\right.$ was found in lateral film direction. This value is the highest value known for hydrogen diffusion in Mg-dihydride, at room temperature. Possible sources for this high lateral hydrogen diffusivity are discussed including preferential hydrogen diffusion along the Mg/Mg-oxide interface, anisotropy of diffusion coefficients and lowering of diffusion energy barrier upon anisotropic film expansion.     

Determination of ammonium turnover and flow patterns close to roots using imaging optodes

The physical effect of nitrogen upon plants has been studied thoroughly; however, direct studies of nitrogen turnover close to roots have been limited by analytical techniques with low spatial and temporal resolution. Thus, little is known about differences in turnover taking place along and between intact root structures over time as well as how root arrangement, root cell type, plant age, microbial activity, and the dark/light cycle influence uptake and supply of nutrients to root structures. In this study an imaging (planar) optode was used to quantify ammonium over time close to an intact root system of a large fruit bearing tomato plant (Lycopersicon esculentum). Images throughout the experiment made it possible to define the ammonium depletion zone and active turnover potential as well as determine turnover rate and flow patterns around the root system over time. The results indicated that ammonium uptake for tomato plants proceeds over the entire root structure but transverse thin peripheral roots are about twice as efficient as the main root and that the uptake process might influence nutrient availability. The flow patterns close to the root structure revealed that apical regions seem to have a central role in ammonium acquisition.     

High-Temperature Phase Equilibria of Duplex Stainless Steels Assessed with a Novel <Emphasis Type="Italic">In-Situ</Emphasis> Neutron Scattering Approach

Duplex stainless steels are designed to solidify with ferrite as the parent phase, with subsequent austenite formation occurring in the solid state, implying that, thermodynamically, a fully ferritic range should exist at high temperatures. However, computational thermodynamic tools appear currently to overestimate the austenite stability of these systems, and contradictory data exist in the literature. In the present work, the high-temperature phase equilibria of four commercial duplex stainless steel grades, denoted 2304, 2101, 2507, and 3207, with varying alloying levels were assessed by measurements of the austenite-to-ferrite transformation at temperatures approaching 1673 K (1400 °C) using a novel in-situ neutron scattering approach. All grades became fully ferritic at some point during progressive heating. Higher austenite dissolution temperatures were measured for the higher alloyed grades, and for 3207, the temperature range for a single-phase ferritic structure approached zero. The influence of temperatures in the region of austenite dissolution was further evaluated by microstructural characterization using electron backscattered diffraction of isothermally heat-treated and quenched samples. The new experimental data are compared to thermodynamic calculations, and the precision of databases is discussed.     

Some Aspects of the Melting and Dephosphorization Mechanism of Hydrogen-DRI

To meet the future environmental challenges, hydrogen direct reduced iron (H-DRI) is expected to constitute the principal material for virgin steel production. For an efficient value chain, knowledge of the melting mechanism and dephosphorization mechanism of H-DRI is needed. The in situ melting behavior, the melting mechanism, and the dephosphorization mechanism during heating of H-DRI are investigated experimentally at 1773 and 1873 K. It is found that the melting rate of H-DRI varies with the reduction degree (91–99.5%), increasing with decreasing reduction degree. An autogenous slag forms during heating and flows through the pores of the H-DRI, thus increasing its effective thermal conductivity. The fraction of filled pores varies with reduction degree explaining the difference in melting rate. At this stage, the dissolution of apatite is initiated and completed upon melting of the metal phase. A gradual reversion of phosphorus from the autogenous slag to the liquid metal is observed after complete melting. The rate of reversion is discussed based on the properties of the H-DRI, for example, reduction degree and carbon addition.     

From Microbial Succinic Acid Production to Polybutylene Bio-Succinate Synthesis

A simplified and scalable one-pot process for the anaerobic production of succinic acid using a metabolically engineered Corynebacterium glutamicum strain is demonstrated. With targeted bioprocess optimization, succinic acid titer of 78 g L⁻¹ and yield of 1.41 mol_SAmol_GLC⁻¹ were achieved. Succinic acid was recovered from the neutral fermentation broth by electrochemically induced crystallization and applied for polybutylene bio-succinate synthesis using a biocompatible zinc catalyst. Except for a slight color change, the final biopolymer was comparable to the polymer from commercial precursors.     

Precipitation Kinetics During Post-heat Treatment of an Additively Manufactured Ferritic Stainless Steel

Metallurgical and Materials Transactions A - The microstructure response of laser-powder bed fusion (L-PBF)-processed ferritic stainless steel (AISI 441) during post-heat treatments is studied in...     

99mTc-HDP Labeling—A Non-Destructive Method for Real-Time Surveillance of the Osteogenic Differentiation Potential of hMSC during Ongoing Cell Cultures

99-Metastabil Technetium (^99mTc) is a radiopharmaceutical widely used in skeletal scintigraphy. Recent publications show it can also be used to determine the osteogenic potential of human mesenchymal stem cells (hMSCs) by binding to hydroxyapatite formed during bone tissue engineering. This field lacks non-destructive methods to track live osteogenic differentiation of hMSCs. However, no data about the uptake kinetics of ^99mTc and its effect on osteogenesis of hMSCs have been published yet. We therefore evaluated the saturation time of ^99mTc by incubating hMSC cultures for different periods, and the saturation concentration by using different amounts of ^99mTc activity for incubation. The influence of ^99mTc on osteogenic potential of hMSCs was then evaluated by labeling a continuous hMSC culture three times over the course of 3 weeks, and comparing the findings to cultures labeled once. Our findings show that ^99mTc saturation time is less than 0.25 h, and saturation concentration is between 750 and 1000 MBq. Repeated exposure to γ-radiation emitted by ^99mTc had no negative effects on hMSC cultures. These new insights can be used to make this highly promising method broadly available to support researchers in the field of bone tissue engineering using this method to track and evaluate, in real-time, the osteogenic differentiation of hMSC, without any negative influence on the cell viability, or their osteogenic differentiation potential.     

Silica‐Based,Organically Modified Host Material for Waveguide Structuring by Two‐Photon‐Induced Photopolymerization

The three‐dimensional fabrication of optical waveguides has gained increasing interest in recent years to establish interconnections between electrical components on a very small scale where copper circuits encounter severe limitations. In this work the application of optically clear, organically modified porous silica monoliths and thin films as a host material for polymeric waveguides to be inscribed into the solid host structure by two‐photon‐induced photopolymerization is investigated. Porosity is generated using a lyotropic liquid crystalline surfactant/solvent system as a template for the solid silica material obtained by a sol–gel transition of a liquid precursor. In order to reduce the brittleness of the purely inorganic material, organic–inorganic co‐precursor molecules that contain poly(ethylene glycol) chains are synthesized and added to the mixture, which successfully suppresses macroscopic cracking and leads to flexible thin films. The structure of the thus‐obtained porous organic–inorganic hybrid material is investigated by atomic force microscopy. It is shown that the modified material is suitable for infiltration with photocurable monomers and functional polymeric waveguides can be inscribed by selective two‐photon‐induced photopolymerization.     

Urinary Tract Tumor Organoids Reveal Eminent Differences in Drug Sensitivities When Compared to 2-Dimensional Culture Systems

Generation of organoids from urinary tract tumor samples was pioneered a few years ago. We generated organoids from two upper tract urothelial carcinomas and from one bladder cancer sample, and confirmed the expression of cytokeratins as urothelial antigens, vimentin as a mesenchymal marker, and fibroblast growth factor receptor 3 by immunohistochemistry. We investigated the dose response curves of two novel components, venetoclax versus {"type":"entrez-nucleotide","attrs":{"text":"S63845","term_id":"400540","term_text":"S63845"}}S63845, in comparison to the clinical standard cisplatin in organoids in comparison to the corresponding two-dimensional cultures. Normal urothelial cells and tumor lines RT4 and HT1197 served as controls. We report that upper tract urothelial carcinoma cells and bladder cancer cells in two-dimensional cultures yielded clearly different sensitivities towards venetoclax, {"type":"entrez-nucleotide","attrs":{"text":"S63845","term_id":"400540","term_text":"S63845"}}S63845, and cisplatin. Two-dimensional cultures were more sensitive at low drug concentrations, while organoids yielded higher drug efficacies at higher doses. In some two-dimensional cell viability experiments, colorimetric assays yielded different IC₅₀ toxicity levels when compared to chemiluminescence assays. Organoids exhibited distinct sensitivities towards cisplatin and to a somewhat lesser extent towards venetoclax or {"type":"entrez-nucleotide","attrs":{"text":"S63845","term_id":"400540","term_text":"S63845"}}S63845, respectively, and significantly different sensitivities towards the three drugs investigated when compared to the corresponding two-dimensional cultures. We conclude that organoids maintained inter-individual sensitivities towards venetoclax, {"type":"entrez-nucleotide","attrs":{"text":"S63845","term_id":"400540","term_text":"S63845"}}S63845, and cisplatin. The preclinical models and test systems employed may bias the results of cytotoxicity studies.