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排序方式: 共有137条查询结果,搜索用时 15 毫秒
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Niklas L. P. Lundström Kaj Nyström Marcus Olofsson 《Annali di Matematica Pura ed Applicata》2014,193(4):1213-1247
In this paper we study the system $$\begin{aligned}&\min \biggl \{-\mathcal H u_i(x,t)-\psi _i(x,t),u_i(x,t)-\max _{j\ne i}(-c_{i,j}(x,t)+u_j(x,t))\biggr \}=0,\\&u_i(x,T)=g_i(x),\ i\in \{1,\ldots ,d\}, \end{aligned}$$ where \((x,t)\in \mathbb R ^{N}\times [0,T]\) . A special case of this type of system of variational inequalities with terminal data occurs in the context of optimal switching problems. We establish a general comparison principle for viscosity sub- and supersolutions to the system under mild regularity, growth, and structural assumptions on the data, i.e., on the operator \(\mathcal H \) and on continuous functions \(\psi _i\) , \(c_{i,j}\) , and \(g_i\) . A key aspect is that we make no sign assumption on the switching costs \(\{c_{i,j}\}\) and that \(c_{i,j}\) is allowed to depend on \(x\) as well as \(t\) . Using the comparison principle, the existence of a unique viscosity solution \((u_1,\ldots ,u_d)\) to the system is constructed as the limit of an increasing sequence of solutions to associated obstacle problems. Having settled the existence and uniqueness, we subsequently focus on regularity of \((u_1,\ldots ,u_d)\) beyond continuity. In this context, in particular, we assume that \(\mathcal H \) belongs to a class of second-order differential operators of Kolmogorov type of the form: $$\begin{aligned} \mathcal H =\sum _{i,j=1}^m a_{i,j}(x,t)\partial _{x_i x_j}+\sum _{i=1}^m a_i(x,t)\partial _{x_i} +\sum _{i,j=1}^N b_{i,j}x_i\partial _{x_j}+\partial _t, \end{aligned}$$ where \(1\le m\le N\) . The matrix \(\{a_{i,j}(x,t)\}_{i,j=1,\ldots ,m}\) is assumed to be symmetric and uniformly positive definite in \(\mathbb R ^m\) . In particular, uniform ellipticity is only assumed in the first \(m\) coordinate directions, and hence, \(\mathcal H \) may be degenerate. 相似文献
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Diana Carolina Figueroa Murcia Philip L. Fosbøl Kaj Thomsen Erling H. Stenby 《Journal of solution chemistry》2017,46(9-10):1805-1817
A new experimental set-up and methodology for the measurement of ZnS solubility in aqueous solutions at 40, 60 and 80 °C (atmospheric pressure) is presented. The methodology implemented includes the preparation of the samples in a reduced oxygen atmosphere, particle size analysis of ZnS, quality control of the analytical technique and evaluation of equilibration time. ZnS solubility analyses were run for prolonged times (up to 11 days) to ensure that equilibrium conditions were met. The equilibration time was explored at three temperatures (40, 60 and 80 °C) observing small variations in the time required to reach the solid–liquid equilibrium at each temperature. Equilibrium was reached within 72 h. The concentration of zinc and of total sulfur were determined using Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES). The experimental solubility data show an exponential dependency of the solubility with respect to temperature. An increase of 40 °C results in an increase of roughly 12 times for the solubility of ZnS. 相似文献
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Thorsell A Portelius E Blennow K Westman-Brinkmalm A 《Rapid communications in mass spectrometry : RCM》2007,21(5):771-778
Mass spectrometric methods based on stable isotopes have shown great promise for identification and quantitation of complex mixtures. Stable isotope labelling by amino acids in cell culture (SILAC) is a straightforward and accurate procedure for quantitation of proteins from cell lines, that are cultured in media containing the natural amino acid or its isotopically labelled analogue, giving rise to either 'light' or 'heavy' proteins. The two cell populations are pooled and treated as a single sample, which allows the use of various protein purification methods without introducing errors into the quantitative analysis. The quantitation of the proteins is based on the intensities of the light and heavy peptides. The increased number of peptides in a quantitative experiment arising from peptide pairs implies that prefractionation is critical prior to liquid chromatography/mass spectrometric (LC/MS) analysis to minimise signal suppression effects and errors in measurements of the intensity ratios. In this study, the effect of a prefractionation step on identification and quantitation of proteins in a SILAC experiment was evaluated. We show that micro-scale liquid-phase isoelectric focusing in the Micro Rotofor separates proteins into well-defined fractions and reduces the sample complexity. Furthermore, the fractionation enhanced the number of identified proteins and improved their quantitation. 相似文献
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A. Radváková O.N. Kazheva O.A. Dyachenko M. Kajňaková V.A. Starodub 《Journal of Physics and Chemistry of Solids》2010,71(5):752-757
We performed the synthesis of a (N-Me-3,5-di-Me-Py)(TCNQ)2 single crystal and we resolved the crystallic and molecular structure of this salt. Magnetic susceptibility measurements were performed in the temperature range 2-300 K. The results are studied with respect to two energy gaps in the magnetic excitations spectra which could signify that the Peierls dielectric phase forms in two grades. 相似文献
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Sandra S. Nurttila Dr. Wolfgang Brenner Dr. Jesús Mosquera Kaj M. van Vliet Prof. Dr. Jonathan R. Nitschke Prof. Dr. Joost N. H. Reek 《Chemistry (Weinheim an der Bergstrasse, Germany)》2019,25(2):609-620
Size-selective hydroformylation of terminal alkenes was attained upon embedding a rhodium bisphosphine complex in a supramolecular metal–organic cage that was formed by subcomponent self-assembly. The catalyst was bound in the cage by a ligand-template approach, in which pyridyl–zinc(II) porphyrin interactions led to high association constants (>105 m −1) for the binding of the ligands and the corresponding rhodium complex. DFT calculations confirm that the second coordination sphere forces the encapsulated active species to adopt the ee coordination geometry (i.e., both phosphine ligands in equatorial positions), in line with in situ high-pressure IR studies of the host–guest complex. The window aperture of the cage decreases slightly upon binding the catalyst. As a result, the diffusion of larger substrates into the cage is slower compared to that of smaller substrates. Consequently, the encapsulated rhodium catalyst displays substrate selectivity, converting smaller substrates faster to the corresponding aldehydes. This selectivity bears a resemblance to an effect observed in nature, where enzymes are able to discriminate between substrates based on shape and size by embedding the active site deep inside the hydrophobic pocket of a bulky protein structure. 相似文献
48.
We present an algorithm for minimax optimization that combines LP methods and quasi-Newton methods. The quasi-Newton algorithm is used only if an irregular solution is detected, in which case second-order derivative information is needed in order to obtain a fast final rate of convergence. We prove that the algorithm can converge only to a stationary point and that normally the final rate of convergence will be either quadratic or superlinear. The performance is illustrated through some numerical examples. 相似文献
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