Coking behavior of nickel and a rhodium based catalyst used in steam reforming for power-to-gas applications

This paper proposes partial steam reforming of natural gas as a chemical storage option for excess electricity. Thermodynamic simulations with Aspen Plus^® show that highest process efficiencies are reached at low steam-to-carbon (S/C) ratios in the feed. However, coke deposition due to unwanted side or follow-up reactions and thus catalyst deactivation is likely in this operation range. In an experimental evaluation three catalysts were selected to test their resistance towards coking: two nickel based and one rhodium based noble metal catalyst. They were tested regarding their long-term stability at S/C ratios as low as 0 to 0.1 and reaction temperatures between 450 and 500 °C. A different reaction and deactivation behavior was observed for nickel and the noble metal catalysts. The measured life times of the noble metal catalyst were by a factor of at least 100 higher than for the two selected nickel catalysts at the applied reforming conditions. Furthermore, after each reforming experiment, a temperature-programmed oxidation (TPO) analysis was performed for the spent catalysts. Based on literature data, the measured CO₂ peaks at corresponding temperatures were related to the different forms of solid carbon depositions. Main carbonaceous species found on the nickel catalysts were of filamentous nature, whereas one or two more reactive C species with monoatomic or polymeric structure at much lower amount were detected on the noble metal catalyst. Further SEM analysis confirmed these findings.     

High‐TC Interfacial Ferromagnetism in SrMnO3/LaMnO3 Superlattices

Heterostructures of strongly correlated oxides demonstrate various intriguing and potentially useful interfacial phenomena. LaMnO₃/SrMnO₃ superlattices are presented showcasing a new high‐temperature ferromagnetic phase with Curie temperature, T_C ≈360 K, caused by electron transfer from the surface of the LaMnO₃ donor layer into the neighboring SrMnO₃ acceptor layer. As a result, the SrMnO₃ (top)/LaMnO₃ (bottom) interface shows an enhancement of the magnetization as depth‐profiled by polarized neutron reflectometry. The length scale of charge transfer, λ_TF ≈2 unit cells, is obtained from in situ growth monitoring by optical ellipsometry, supported by optical simulations, and further confirmed by high resolution electron microscopy and spectroscopy. A model of the inhomogeneous distribution of electron density in LaMnO₃/SrMnO₃ layers along the growth direction is concluded to account for a complex interplay between ferromagnetic and antiferromagnetic layers in superlattices.     

Prediction of highway lane changes based on prototype trajectories

Forschung im Ingenieurwesen - The vision of automated driving is to increase both road safety and efficiency, while offering passengers a convenient travel experience. This requires that...     

Viologen capped by nucleobase—building blocks for functional materials: synthesis and structure–properties relationship

Journal of Materials Science - The current study presents a new class of functional derivatives (1–3) consisting of a dicationic viologen (4,4’-bipyridinium unit) (V2+) capped by...     

Site-directed mutants of the cAMP receptor protein-DNA binding of five mutant proteins

Oligonucleotide-directed mutagenesis was employed to generatemutants of the cAMP receptor protein (CRP) of Escherichia coli.The mutant proteins were purified to homogeneity and testedfor stability and DNA binding. It is shown that mutations atthe position of Arg¹⁸⁰ abolish specific DNA binding, whereasthose at the position Arg¹⁸⁵ have very little effect. Both positionshave previously been implicated as crucial for the specificinteraction between CRP and DNA. The Ser¹²⁸ Ala mutant showsa slight reduction in DNA binding affinity relative to wild-type.All mutants investigated show similar stability profiles towild-type CRP with respect to thermolysin proteolysis as a functionof temperature.     

Film Forming Behavior of Greases Under Starved and Fully Flooded EHL Conditions

Improving knowledge on the film forming behavior of greases is essential to be able to develop efficient greases. This article examines how operating conditions (e.g., temperature, lubrication condition [fully flooded/starved]) and base oil viscosity influence the film forming properties of greases by comparing the behavior of two lithium-based greases and their respective base oils in rolling point contact. It is found that the onset and degree of starvation is controlled by speed (u) × viscosity (ν)/load (W) factor (uν/W) and temperature and that low uν/W values promote entrainment of thickener into contact. Thus, grease with low base oil viscosity shows significant thickener entrainment in the low speed region compared to the one with high base oil viscosity, which leads to the formation of thickener-rich viscous material during extended running with the low base oil viscosity grease. The results suggest that the shape of the film thickness versus speed curve is viscosity and uν/W range dependent. Furthermore, for the test conditions used in this study, grease-lubricated contacts appear to shift from the initial fully flooded condition to starved condition over a prolonged running of 2 h. The results from this study concur with those reported in the literature that fully flooded oil elastohydrodynamic lubrication (EHL) theory or film thickness cannot be directly applied or taken as a guideline in grease-lubricated contacts.     

A Unitary Analysis of some Voltage and Current Mode Linear Circuits

This paper presents a systematic and unitary analysis of a large class of current and voltage mode circuits based on a series-shunt-like configuration. Four possible OA types are considered for the basic amplifier. The amplifiers have voltage and current input signals and voltage and current outputs. The analysis method is based on the separation of the circuit signal graph in two different paths, one that controls the gain and the other that controls the bandwidth.     

Retarding Thermal Degradation in Hybrid Perovskites by Ionic Liquid Additives

Recent years have witnessed considerable progress in the development of solar cells based on lead halide perovskite materials. However, their intrinsic instability remains a limitation. In this context, the interplay between the thermal degradation and the hydrophobicity of perovskite materials is investigated. To this end, the salt 1‐(4‐ethenylbenzyl)‐3‐(3,3,4,4,5,5,6,6,7,7,8,8,8‐tridecafluorooctylimidazolium iodide (ETI), is employed as an additive in hybrid perovskites, endowing the photoactive materials with high thermal stability and hydrophobicity. The ETI additive inhibits methylammonium (MA) permeation in methylammonium lead triiodide (MAPbI₃) occurring due to intrinsic thermal degradation, by inhibiting out‐diffusion of the MA⁺ cation, preserving the pristine material and preventing decomposition. With this simple approach, high efficiency solar cells based on the unstable MAPbI₃ perovskite are markedly stabilized under maximum power point tracking, leading to greater than twice the preserved efficiency after 700 h of continuous light illumination and heating (60 °C). These results suggest a strategy to tackle the intrinsic thermal decomposition of MAI, an essential component in all state‐of‐the‐art perovskite compositions.