6,567 research outputs found
Carbon dioxide free production of hydrogen
The present report summarizes the theoretical modelling and experimental investigation results of the study on the direct thermal methane cracking. This work is a part of the
LIMTECH-Project (Liquid Metal Technologies) funded of Helmholtz Alliance and was carried
out from 2012 to 2017. The Project-part B5 “CO2-free production of hydrogen” focused on
experimental testing and particularly on modelling the novel methane cracking method
based on liquid metal technology. The new method uses a bubble column reactor, filled
with liquid metal, where both the chemical reaction of methane decomposition and the separation of gas fraction from solid carbon occur. Such reactor system was designed and built in the liquid metal laboratory (KALLA) at KIT. The influences of liquid metal temperature distribution in reactor and feed gas flow rate on methane conversion ratio were investigated experimentally at the temperature range from 930°C to 1175 °C and methane flow rate at the
reactor inlet from 50 to 200 mLn/min. In parallel with experimental investigations, a thermochemical model, giving insight in the influence of the above mentioned parameters has been developed at KIT and a CFD model was developed at LUH to get an overview about the bubble dynamics in the reaction system. The influence of different bubble sizes and shapes,
multi-inlet coalescence effects as well as the potential of electromagnetic stirring have been
investigated
Carbon dioxide free production of hydrogen
The present report summarizes the theoretical modelling and experimental investigation results of the study on the direct thermal methane cracking. This work is a part of the LIMTECH-Project (Liquid Metal Technologies) funded of Helmholtz Alliance and was carried out from 2012 to 2017. The Project-part B5 "CO2-free production of hydrogen" focused on experimental testing and particularly on modelling the novel methane cracking method based on liquid metal technology. The new method uses a bubble column reactor, filled with liquid metal, where both the chemical reaction of methane decomposition and the separation of gas fraction from solid carbon occur. Such reactor system was designed and built in the liquid metal laboratory (KALLA) at KIT. The influences of liquid metal temperature distribution in reactor and feed gas flow rate on methane conversion ratio were investigated experimentally at the temperature range from 930 C to 1175 C and methane flow rate at the reactor inlet from 50 to 200 mLn/min. In parallel with experimental investigations, a thermochemical model, giving insight in the influence of the above mentioned parameters has been developed at KIT and a CFD model was developed at LUH to get an overview about the bubble dynamics in the reaction system. The influence of different bubble sizes and shapes, multi-inlet coalescence effects as well as the potential of electromagnetic stirring have been investigated
TECPR1 promotes aggrephagy by direct recruitment of LC3C autophagosomes to lysosomes
The accumulation of protein aggregates is involved in the onset of many neurodegenerative diseases. Aggrephagy is a selective type of autophagy that counteracts neurodegeneration by degrading such aggregates. In this study, we found that LC3C cooperates with lysosomal TECPR1 to promote the degradation of disease-related protein aggregates in neural stem cells. The N-terminal WD-repeat domain of TECPR1 selectively binds LC3C which decorates matured autophagosomes. The interaction of LC3C and TECPR1 promotes the recruitment of autophagosomes to lysosomes for degradation. Augmented expression of TECPR1 in neural stem cells reduces the number of protein aggregates by promoting their autophagic clearance, whereas knockdown of LC3C inhibits aggrephagy. The PH domain of TECPR1 selectively interacts with PtdIns(4)P to target TECPR1 to PtdIns(4)P containing lysosomes. Exchanging the PH against a tandem-FYVE domain targets TECPR1 ectopically to endosomes. This leads to an accumulation of LC3C autophagosomes at endosomes and prevents their delivery to lysosomes. Many neurodegenerative disorders are characterised by the accumulation of protein aggregates in neurons. Here, the authors show that the lysosomal protein TECPR1 selectively recruits mature autophagosomes via an interaction with LC3C to break down protein aggregates in neural stem cells
Molecular basis for passive immunotherapy of Alzheimer's disease
Amyloid aggregates of the amyloid-{beta} (A{beta}) peptide are implicated in the pathology of Alzheimer's disease. Anti-A{beta} monoclonal antibodies (mAbs) have been shown to reduce amyloid plaques in vitro and in animal studies. Consequently, passive immunization is being considered for treating Alzheimer's, and anti-A{beta} mAbs are now in phase II trials. We report the isolation of two mAbs (PFA1 and PFA2) that recognize A{beta} monomers, protofibrils, and fibrils and the structures of their antigen binding fragments (Fabs) in complex with the A{beta}(1–8) peptide DAEFRHDS. The immunodominant EFRHD sequence forms salt bridges, hydrogen bonds, and hydrophobic contacts, including interactions with a striking WWDDD motif of the antigen binding fragments. We also show that a similar sequence (AKFRHD) derived from the human protein GRIP1 is able to cross-react with both PFA1 and PFA2 and, when cocrystallized with PFA1, binds in an identical conformation to A{beta}(1–8). Because such cross-reactivity has implications for potential side effects of immunotherapy, our structures provide a template for designing derivative mAbs that target A{beta} with improved specificity and higher affinity
Doppler tissue imaging to localize accessory pathways in pediatric patients with Wolff-Parkinson-White syndrome
A New Look at the Axial Anomaly in Lattice QED with Wilson Fermions
By carrying out a systematic expansion of Feynman integrals in the lattice
spacing, we show that the axial anomaly in the U(1) lattice gauge theory with
Wilson fermions, as determined in one-loop order from an irrelevant lattice
operator in the Ward identity, must necessarily be identical to that computed
from the dimensionally regulated continuum Feynman integrals for the triangle
diagrams.Comment: 1 figure, LaTeX, 18 page
Chirality in Bare and Passivated Gold Nanoclusters
Chiral structures have been found as the lowest-energy isomers of bare
(Au and Au_{28}(SCH_{16}_{38}(SCH_{3})_{24}) gold nanoclusters. The degree of chirality existing in
the chiral clusters was calculated using the Hausdorff chirality measure. We
found that the index of chirality is higher in the passivated clusters and
decreases with the cluster size. These results are consistent with the observed
chiroptical activity recently reported for glutahione-passivated gold
nanoclusters, and provide theoretical support for the existence of chirality in
these novel compounds.Comment: 5 pages, 1 figure. Submitted to PR
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