A mixed-integer LP model for the reconfiguration of radial electric distribution systems considering distributed generation

The problem of reconfiguration of distribution systems considering the presence of distributed generation is modeled as a mixed-integer linear programming (MILP) problem in this paper. The demands of the electric distribution system are modeled through linear approximations in terms of real and imaginary parts of the voltage, taking into account typical operating conditions of the electric distribution system. The use of an MILP formulation has the following benefits: (a) a robust mathematical model that is equivalent to the mixed-integer non-linear programming model; (b) an efficient computational behavior with exiting MILP solvers; and (c) guarantees convergence to optimality using classical optimization techniques. Results from one test system and two real systems show the excellent performance of the proposed methodology compared with conventional methods. © 2012 Published by Elsevier B.V. All rights reserved.

A mixed-integer LP model for the optimal allocation of voltage regulators and capacitors in radial distribution systems

This paper presents a mixed-integer linear programming model to solve the problem of allocating voltage regulators and fixed or switched capacitors (VRCs) in radial distribution systems. The use of a mixed-integer linear model guarantees convergence to optimality using existing optimization software. In the proposed model, the steady-state operation of the radial distribution system is modeled through linear expressions. The results of one test system and one real distribution system are presented in order to show the accuracy as well as the efficiency of the proposed solution technique. An heuristic to obtain the Pareto front for the multiobjective VRCs allocation problem is also presented. © 2012 Elsevier Ltd. All rights reserved.

Soluções auto-similares das equações de Navier-Stokes em Lp-Fraco

Pós-graduação em Matemática - IBILCE

Caracterização mecânica e estrutural de um dispositivo PDLC baseado em hidrogéis de PAAm e cristal líquido liotrópico LP/DeOH/H2O

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Boa colocação da equação quase-geostrófica em Lp-fraco

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Die Rolle der Autoimmunreaktion gegen das SLA/LP-Molekül bei autoimmuner Hepatitis

In der vorliegenden Arbeit wurde die Rolle des SLA/LP Proteins bei der autoimmunen Hepatits untersucht. Zum einen sollte die Hypothese einer aberranten Expression des SLA/LP Moleküls als Auslöser der Autoimmunreaktion gegen SLA/LP überprüft werden. Hierzu wurde die Expression des SLA/LP Moleküls in Leber und Lymphozyten von Patienten mit verschiedenen hepatischen Erkrankungen und bei gesunden Personen bestimmt. Die quantitativen Expressionsanalysen wurden mittels real-time PCR unter Einsatz SLA/LP-spezifischer Oligonukleotide durchgeführt. Es zeigte sich, dass SLA/LP ubiquitär im Körper exprimiert wird, mit erhöhter Expression im Pankreas. Die Ergebnisse der SLA/LP Expressionsanalysen in peripheren mononukleären Blutzellen und Leberparenchymzellen von Patienten mit einer autoimmunen Hepatitis ergaben keine Hinweise auf eine aberrante Expression des SLA/LPs. Es konnte gezeigt werden, dass SLA/LP im Leberparenchym der Patienten tendenziell eher erhöht exprimiert wird, doch war kein Unterschied zwischen unterschiedlichen hepatischen Erkrankungen nachweisbar. Somit konnte in dieser Arbeit gezeigt werden, dass eine aberrante Expression nicht für die Auslösung der Erkrankung zuständig ist. Zum andern sollte in dieser Arbeit überprüft werden, ob eine Autoimmunreaktion gegen SLA/LP zu einer Entzündung in der Leber führen kann. Hierzu wurden Mäuse unterschiedlicher Stämme mit SLA/LP Protein in komplettem Freunds Adjuvans immunisiert und auf Leberschädigung und Leberentzündung untersucht. Es konnte gezeigt werden, dass SLA/LP-Autoimmunität Leberentzündung und Leberschädigung auslösen kann. Die Auslösung der Hepatitis war aber vom Mausstamm und der Defizienz von Interleukin 10 abhängig. Somit scheint unter bestimmten immunologischen Bedingungen eine Immunreaktion gegen SLA/LP zu einer Leberentzündung und Leberschädigung zu führen.

Toward a Magnitude Scale for Low Frequency Seismicity The LP energy for Campi Flegrei caldera

The energy released during a seismic crisis in volcanic areas is strictly related to the physical processes in the volcanic structure. In particular Long Period seismicity, that seems to be related to the oscillation of a fluid-filled crack (Chouet , 1996, Chouet, 2003, McNutt, 2005), can precedes or accompanies an eruption. The present doctoral thesis is focused on the study of the LP seismicity recorded in the Campi Flegrei volcano (Campania, Italy) during the October 2006 crisis. Campi Flegrei Caldera is an active caldera; the combination of an active magmatic system and a dense populated area make the Campi Flegrei a critical volcano. The source dynamic of LP seismicity is thought to be very different from the other kind of seismicity ( Tectonic or Volcano Tectonic): it’s characterized by a time sustained source and a low content in frequency. This features implies that the duration–magnitude, that is commonly used for VT events and sometimes for LPs as well, is unadapted for LP magnitude evaluation. The main goal of this doctoral work was to develop a method for the determination of the magnitude for the LP seismicity; it’s based on the comparison of the energy of VT event and LP event, linking the energy to the VT moment magnitude. So the magnitude of the LP event would be the moment magnitude of a VT event with the same energy of the LP. We applied this method to the LP data-set recorded at Campi Flegrei caldera in 2006, to an LP data-set of Colima volcano recorded in 2005 – 2006 and for an event recorded at Etna volcano. Experimenting this method to lots of waveforms recorded at different volcanoes we tested its easy applicability and consequently its usefulness in the routinely and in the quasi-real time work of a volcanological observatory.

Heuristic decomposition and LP-based scheduling in make-and-pack production

In this paper, we are concerned about the short-term scheduling of industrial make-and-pack production processes. The planning problem consists in minimizing the production makespan while meeting given end-product demands. Sequence-dependent changeover times, multi-purpose storage units with finite capacities, quarantine times, batch splitting, partial equipment connectivity, material transfer times, and a large number of operations contribute to the complexity of the problem. Known MILP formulations cover all technological constraints of such production processes, but only small problem instances can be solved in reasonable CPU times. In this paper, we develop a heuristic in order to tackle large instances. Under this heuristic, groups of batches are scheduled iteratively using a novel MILP formulation; the assignment of the batches to the groups and the scheduling sequence of the groups are determined using a priority rule. We demonstrate the applicability by means of a real-world production process.

Fine-mapping and mutation analysis of TRPM1: a candidate gene for leopard complex (LP) spotting and congenital stationary night blindness in horses.

Leopard Complex spotting occurs in several breeds of horses and is caused by an incompletely dominant allele (LP). Homozygosity for LP is also associated with congenital stationary night blindness (CSNB) in Appaloosa horses. Previously, LP was mapped to a 6 cm region on ECA1 containing the candidate gene TRPM1 (Transient Receptor Potential Cation Channel, Subfamily M, Member 1) and decreased expression of this gene, measured by qRT-PCR, was identified as the likely cause of both spotting and ocular phenotypes. This study describes investigations for a mutation causing or associated with the Leopard Complex and CSNB phenotype in horses. Re-sequencing of the gene and associated splice sites within the 105 624 bp genomic region of TRPM1 led to the discovery of 18 SNPs. Most of the SNPs did not have a predictive value for the presence of LP. However, one SNP (ECA1:108,249,293 C>T) found within intron 11 had a strong (P < 0.0005), but not complete, association with LP and CSNB and thus is a good marker but unlikely to be causative. To further localize the association, 70 SNPs spanning over two Mb including the TRPM1 gene were genotyped in 192 horses from three different breeds segregating for LP. A single 173 kb haplotype associated with LP and CSNB (ECA1: 108,197,355- 108,370,150) was identified. Illumina sequencing of 300 kb surrounding this haplotype revealed 57 SNP variants. Based on their localization within expressed sequences or regions of high sequence conservation across mammals, six of these SNPs were considered to be the most likely candidate mutations. While the precise function of TRPM1 remains to be elucidated, this work solidifies its functional role in both pigmentation and night vision. Further, this work has identified several potential regulatory elements of the TRPM1 gene that should be investigated further in this and other species.