692 research outputs found
Smart dual thermal network
Conventional district heating (DH) systems enable demand aggregation at district level and can provide high centralized heat generation performance values. However, thermal Renewable Energy Sources (RES) deployment at building level still remains low, and exploitation suboptimal, as it is limited by the instantaneous thermal load and storage capacity availability of each building. Buildings play the role of consumers that request a variable amount of heat over time and the thermal network the role of unidirectional heat supplier, without any smart interaction. The FP7 project A2PBEER has developed an innovative Smart Dual Thermal Network concept based on RES and Combined Heat and Power (CHP) as generation technologies, that enables transforming existing suboptimal DH systems, into integrated thermal networks with optimized performance and building level RES system production exploitation. It is based on an innovative Smart Dual Building Thermal Substation concept, which allows a bidirectional heat exchange of the buildings with the thermal network, and to aggregate district level distributed production and storage capacity (Virtual District Plant). With this approach buildings become prosumers maximizing decentralized RES production exploitation, as any possible local heat production surplus on any building of the district, will be delivered to the network to be used by other buildings. Additionally, this thermal network allows the delivery of the energy necessary to meet the heating and cooling demand of the buildings through a single hot water distribution network. In this way, it is possible to upgrade conventional DH systems to district heating and cooling systems, without the construction of a district cooling plant and a dedicated cooling distribution network. Cooling is produced at building level through sorption technologies using locally deployed solar collectors and the thermal network as energy sources. Finally, the district typologies and climatic conditions that maximize the potential of this thermal network concept have been identified.The research activities leading to the described developments and results, were funded by the FP7 project A2PBEER, under grant agreement No 906090. Special thanks to Olof Hallström and ClimateWell AB for making the TRNSYS model of the innovative sorption system and developing the component level simulation work
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An Efficient Switch Model for Simulating Large Power Systems with Many Power Converters
Frequent matrix factorizations due to power electronic switch commutations are computationally expensive. This paper addresses this burden by treating power electronic switches as dependant sources instead of time-varying resistors. The resulting network matrix is constant, and does not require re-factorization when switches commutate. Three power electronic switches are presented and discussed for both nodal and mesh equation formulations. A case study at the end shows that the run-time for a power system with >200 switches when using the switching approach presented herein can reduce from 8 hours to under 15 minutes, which is a speedup of 40x.Center for Electromechanic
Knowledge-based gene expression classification via matrix factorization
Motivation: Modern machine learning methods based on matrix decomposition techniques, like independent component analysis (ICA) or non-negative matrix factorization (NMF), provide new and efficient analysis tools which are currently explored to analyze gene expression profiles. These exploratory feature extraction techniques yield expression modes (ICA) or metagenes (NMF). These extracted features are considered indicative of underlying regulatory processes. They can as well be applied to the classification of gene expression datasets by grouping samples into different categories for diagnostic purposes or group genes into functional categories for further investigation of related metabolic pathways and regulatory networks.
Results: In this study we focus on unsupervised matrix factorization techniques and apply ICA and sparse NMF to microarray datasets. The latter monitor the gene expression levels of human peripheral blood cells during differentiation from monocytes to macrophages. We show that these tools are able to identify relevant signatures in the deduced component matrices and extract informative sets of marker genes from these gene expression profiles. The methods rely on the joint discriminative power of a set of marker genes rather than on single marker genes. With these sets of marker genes, corroborated by leave-one-out or random forest cross-validation, the datasets could easily be classified into related diagnostic categories. The latter correspond to either monocytes versus macrophages or healthy vs Niemann Pick C disease patients.Siemens AG, MunichDFG (Graduate College 638)DAAD (PPP Luso - Alem˜a and PPP Hispano - Alemanas
Design of 3-Phenylcoumarins and 3-Thienylcoumarins as Potent Xanthine Oxidase Inhibitors: Synthesis, Biological Evaluation, and Docking Studies
Coumarin scaffold has proven to be promising in the development of bioactive agents, such as xanthine oxidase (XO) inhibitors. Novel hydroxylated 3-arylcoumarins were designed, synthesized, and evaluated for their XO inhibition and antioxidant properties. 3-(3’-Bromophenyl)-5,7-dihydroxycoumarin (compound 11) proved to be the most potent XO inhibitor, with an IC50 of 91 nM, being 162 times better than allopurinol, one of the reference controls. Kinetic analysis of compound 11 and compound 5 [3-(4’-bromothien-2’-yl)-5,7-dihydroxycoumarin], the second-best compound within the series (IC50 of 280 nM), has been performed, and both compounds showed a mixed-type inhibition. Both compounds present good antioxidant activity (ability to scavenge ABTS radical) and are able to reduce reactive oxygen species (ROS) levels in H2O2-treated cells. In addition, they proved to be non-cytotoxic in a Caco-2 cells viability assay. Molecular docking studies have been carried out to correlate the compounds’ theoretical and experimental binding affinity to the XO binding pocket
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