Molecular dynamics study on thermal dehydration process of epsomite (MgSO4.7H2O)

Water vapour sorption in salt hydrates is one of the most promising means of compact, low loss and long-term solar heat storage in the built environment. Among all, epsomite (MgSO4·7H2O) excels for its high-energy storage density and vast availability. However, in practical applications, the slow kinetics and evident structural changes during hydration and dehydration significantly jeopardise the heat storage/recovery rate. A molecular dynamics (MD) study is carried out to investigate the thermal properties and structural changes in the thermal dehydration process of the epsomite. The MD simulation is carried out at 450 K and a vapour pressure of 20 mbar, in accordance with experimental heat storage conditions. The study identifies the dehydration as multiple stages from the initial quick water loss and collapse of the crystal framework to the adsorption of water molecules, which inhibits complete dehydration. Further, the anisotropic diffusion behaviour supports the important role of the porous matrix structure in the heat and mass transfer process. The enthalpy changes, partial densities, mass diffusion coefficients of water and radial distribution functions are calculated and compared with corresponding experimental data to support the conclusions

Characterization of sugar alcohols as seasonal heat storage media - experimental and theoretical investigations

Sugar alcohols are under investigation as phase change materials for long term heat storage applications. The thermal performance in such systems is strongly dominated by the nucleation and crystal growth kinetics, which is further linked to the crystal-melt interfacial free energy (surface tension), the latent heat, and the viscosity. We carry out a comprehensive study of sugar alcohols to examine their thermodynamic and kinetic properties, from both experiments and theoretical calculations. The theoretical study follows a bottom-up approach. A generalized AMBER force field obtained from first principle calculations is selected to construct the molecular models. Heat capacity, self-diffusion constant, viscosity, latent heat, and interfacial free energy of selected model materials are calculated through molecular dynamic simulations. In the experimental study, differential scanning calorimetry and viscosity measurements are performed. Also, the kinetics of the crystal growth is examined using a microscope. The experimental results are integrated with the Rozmanov model, and a strong dependence of growth speed on the degree of subcooling is identified. All the experimental measurements are compared with our theoretical work, and the results showed good agreement. The methodologies used in the calculation are proved effective and reliable for future prediction of unknown systems. In this study, the high viscosity and the high interfacial free energy are both found responsible for the sluggish kinetics of nucleation and crystal growth in sugar alcohols

A DFT based equilibrium study on the hydrolysis and the dehydration reactions of MgCl 2

Magnesium chloride hydrates are characterized as promising energy storage materials in the builtenvironment. During the dehydration of these materials, there are chances for the release of harmful HCl gas, which can potentially damage the material as well as the equipment. Hydrolysis reactions in magnesium chloride hydrates are subject of study for industrial applications. However, the information about the possibility of hydrolysis reaction, and its preference over dehydration in energy storage systems is still ambiguous at the operating conditions in a seasonal heat storage system. A density functional theory level study is performed to determine molecular structures, charges, and harmonic frequencies in order to identify the formation of HCl at the operating temperatures in an energy storage system. The preference of hydrolysis over dehydration is quantified by applying thermodynamic equilibrium principles by calculating Gibbs free energies of the hydrated magnesium chloride molecules. The molecular structures of the hydrates (n = 0, 1, 2, 4, and 6) of MgCl2 are investigated to understand the stability and symmetry of these molecules. The structures are found to be noncomplex with almost no meta-stable isomers, which may be related to the faster kinetics observed in the hydration of chlorides compared to sulfates. Also, the frequency spectra of these molecules are calculated, which in turn are used to calculate the changes in Gibbs free energy of dehydration and hydrolysis reactions. From these calculations, it is found that the probability for hydrolysis to occur is larger for lower hydrates. Hydrolysis occurring from the hexa-, tetra-, and dihydrate is only possible when the temperature is increased too fast to a very high value. In the case of the mono-hydrate, hydrolysis may become favorable at high water vapor pressure and at low HCl pressure

LiMeS-Lab:An Integrated Laboratory for the Development of Liquid–Metal Shield Technologies for Fusion Reactors

The liquid metal shield laboratory (LiMeS-Lab) will provide the infrastructure to develop, test, and compare liquid metal divertor designs for future fusion reactors. The main research topics of LiMeS-lab will be liquid metal interactions with the substrate material of the divertor, the continuous circulation and capillary refilling of the liquid metal during intense plasma heat loading and the retention of plasma particles in the liquid metal. To facilitate the research, four new devices are in development at the Dutch Institute for Fundamental Energy Research and the Eindhoven University of Technology: LiMeS-AM: a custom metal 3D printer based on powder bed fusion; LiMeS-Wetting, a plasma device to study the wetting of liquid metals on various substrates with different surface treatments; LiMeS-PSI, a linear plasma generator specifically adapted to operate continuous liquid metal loops. Special diagnostic protection will also be implemented to perform measurements in long duration shots without being affected by the liquid metal vapor; LiMeS-TDS, a thermal desorption spectroscopy system to characterize deuterium retention in a metal vapor environment. Each of these devices has specific challenges due to the presence and deposition of metal vapors that need to be addressed in order to function. In this paper, an overview of LiMeS-Lab will be given and the conceptual designs of the last three devices will be presented.</p

Identification of gene co-regulatory modules and associated cis-elements involved in degenerative heart disease

<p>Abstract</p> <p>Background</p> <p>Cardiomyopathies, degenerative diseases of cardiac muscle, are among the leading causes of death in the developed world. Microarray studies of cardiomyopathies have identified up to several hundred genes that significantly alter their expression patterns as the disease progresses. However, the regulatory mechanisms driving these changes, in particular the networks of transcription factors involved, remain poorly understood. Our goals are (A) to identify modules of co-regulated genes that undergo similar changes in expression in various types of cardiomyopathies, and (B) to reveal the specific pattern of transcription factor binding sites, <it>cis</it>-elements, in the proximal promoter region of genes comprising such modules.</p> <p>Methods</p> <p>We analyzed 149 microarray samples from human hypertrophic and dilated cardiomyopathies of various etiologies. Hierarchical clustering and Gene Ontology annotations were applied to identify modules enriched in genes with highly correlated expression and a similar physiological function. To discover motifs that may underly changes in expression, we used the promoter regions for genes in three of the most interesting modules as input to motif discovery algorithms. The resulting motifs were used to construct a probabilistic model predictive of changes in expression across different cardiomyopathies.</p> <p>Results</p> <p>We found that three modules with the highest degree of functional enrichment contain genes involved in myocardial contraction (n = 9), energy generation (n = 20), or protein translation (n = 20). Using motif discovery tools revealed that genes in the contractile module were found to contain a TATA-box followed by a CACC-box, and are depleted in other GC-rich motifs; whereas genes in the translation module contain a pyrimidine-rich initiator, Elk-1, SP-1, and a novel motif with a GCGC core. Using a naïve Bayes classifier revealed that patterns of motifs are statistically predictive of expression patterns, with odds ratios of 2.7 (contractile), 1.9 (energy generation), and 5.5 (protein translation).</p> <p>Conclusion</p> <p>We identified patterns comprised of putative <it>cis</it>-regulatory motifs enriched in the upstream promoter sequence of genes that undergo similar changes in expression secondary to cardiomyopathies of various etiologies. Our analysis is a first step towards understanding transcription factor networks that are active in regulating gene expression during degenerative heart disease.</p