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排序方式: 共有567条查询结果,搜索用时 15 毫秒
1.
The paper presents a new formulation of the integral boundary element method (BEM) using subdomain technique. A continuous approximation of the function and the function derivative in the direction normal to the boundary element (further ‘normal flux’) is introduced for solving the general form of a parabolic diffusion‐convective equation. Double nodes for normal flux approximation are used. The gradient continuity is required at the interior subdomain corners where compatibility and equilibrium interface conditions are prescribed. The obtained system matrix with more equations than unknowns is solved using the fast iterative linear least squares based solver. The robustness and stability of the developed formulation is shown on the cases of a backward‐facing step flow and a square‐driven cavity flow up to the Reynolds number value 50 000. Copyright © 2004 John Wiley & Sons, Ltd. 相似文献
2.
Elie Leopold 《Numerical Algorithms》2007,44(4):347-366
In this paper, we give some new explicit relations between two families of polynomials defined by recurrence relations of
all order. These relations allow us to analyze, even in the Sobolev case, how some properties of a family of orthogonal polynomials
are affected when the coefficients of the recurrence relation and the order are perturbed. In a paper we have already given
a method which allows us to study the polynomials defined by a three-term recurrence relation. Also here some generalizations
are given. 相似文献
3.
We investigate function spaces of generalised smoothness of Besov and Triebel–Lizorkin type. Equivalent quasi-norms in terms
of maximal functions and local means are given. An atomic decomposition theorem for this type of spaces is proved.
Mathematics Subject Classification (2000) 46E35 相似文献
4.
Christoph Klingenberg 《Inventiones Mathematicae》1987,89(2):291-317
Ohne Zusammenfassung 相似文献
5.
Yan B Collins N Wheatley J Irving M Leopold K Chan C Shornikov A Fang L Lee A Stock M Zhao J 《Journal of combinatorial chemistry》2004,6(2):255-261
We have developed a high-throughput purification system to purify combinatorial libraries at a 50-100-mg scale with a throughput of 250 samples/instrument/day. We applied an accelerated retention window method to shorten the purification time and targeted one fraction per injection to simplify data tracking, lower QC workload, and simplify the postpurification processing. First, we determined the accurate retention time and peak height for all compounds using an eight-channel parallel LC/UV/MS system, and calculated the specific preparative HPLC conditions for individual compounds. The preparative HPLC conditions include the compound-specific gradient segment for individual compounds with a fixed gradient slope and the compound-specific UV or ELSD threshold for triggering a fraction collection device. A unique solvent composition or solvent strength was programmed for each compound in the preparative HPLC in order to elute all compounds at the same target time. Considering the possible deviation of the predicted retention time, a 1-min window around the target time was set to collect peaks above a threshold based on UV or ELSD detection. Dual column preparative instruments were used to maximize throughput. We have purified more than 500 000 druglike compounds using this system in the past 3 years. We report various components of this high-throughput purification system and some of our purification results. 相似文献
6.
Microchimica Acta - Eine empfindliche spektrophotometrische Methode zur Bestimmung von Kupfer mit Salicyls~iure wurde beschrieben (Molarextinktion ε = 2,4 · 9 105). Die nachweisbaren... 相似文献
7.
Zusammenfassung In der vorliegenden Arbeit wird das Sedimentationsgleichgewicht der Systeme Na6[H2W12O40]—NaCI—H2O und Na6[H2W12O40]—NaClO4— H2O untersucht. Die scheinbare molare Masse Mapp des Natriummetawolframats wird in beiden Systemen als Funktion der Natriummetawolfrarnat-Anfangspartialdichte
0
PX
z gemessen. Durch lineare Extrapolation der Funktion Mapp = Mapp (PP,, ) auf die Polymerelektrolyt-Anfangspartialdichte Null können die Grenzwerte der scheinbaren molaren Masse (Mapp)o ermittelt werden. Aus den (Mapp)o-Werten wird die Abhängigkeit der Größe (ln
PXz
/m
BX
)
mPXz von der NaCI- bzw. NaClO4-Molalität berechnet.Die Bestimmung der molaren Masse und der (stöchiometrischen) Ladungszahl eines Polymerelektrolyten aus den experimentell ermittelten (Mapp)o-Werten unter Anwendung der Lamm-Williams-Gleichung wird diskutiert. Zur Ermittlung der beiden Größen müssen mehrere Versuchsreihen mit zwei verschiedenen Fremdelektrolyten durchgeführt werden. Externe Messungen sind nicht erforderlich.Man erhält auf diese Weise verläßliche Werte so-wohl der molaren Masse als auch der (stächiometrischen) Ladungszahl.
Mit 5 Abbildungen und 3 Tabellen 相似文献
Summary The sedimentation equilibria of the systems sodium metatungstate-sodium chloride-water and sodium metatungstate-sodium perchlorate-water are investiated. In both systems the apparent molecular mass Mapp of sodium metatungstate (PX z) is measured in dependence on partial density 0 PX z before centrifugation. By linear extrapolation of the function Mapp = Mapp ( 0 PX z the limiting value (Mapp)o for 0 PX z = 0 is obtained. The variation with sodium chloride and sodium perchlorate molality of the quantity (ln PX z m BX )mPXz is calculated from (Mapp)o data.The determination of the molecular mass and the algebraic valency of a polymeric ion by means of the (Mapp)o values calculated by Lamm-Williams equation is discussed. In order to obtain these two quantities at least two series of experiments are required, each of which using a different supporting electrolyte. External measurements are not necessary. In this way reliable values for the molecular mass as well as for the stoichiometric valency are obtained.
Mit 5 Abbildungen und 3 Tabellen 相似文献
8.
Zusammenfassung In der vorliegenden Arbeit wird das Sedimentations-gleichgewicht des Systems Na6[H2W12O40]-NaClO4-H2O bei 25 °C untersucht. Die scheinbare Ladungszahl des Natriummetawolframats wird als Funktion der NaClO4-MolalitätmNaClO4 ermittelt. Aus dieser Abhängigkeit kann für die summarische Dissoziation des NatriummetawolframatsNa2[H2W12O4o] 6Na+ + [H2W12O40]6– die DissoziationskonstanteK in Gegenwart von NaClO4 als Fremdelektrolyt zuK=0,08 mol6·kg–6 bestimmt werden.Der Kreuzdifferentialquotient
(
PXz
, ist der Trace-Aktivitätskoeffizient des Natriummetawolframats) wird ebenfalls als Funktion der NaClO4-Molalität ermittelt.Die Konzentrationsabhängigkeit des Trace-Aktivitätskoeffizienten zeigt einen Verlauf, wie er unseres Wissens nach noch nicht von anderen Autoren beobachtet wurde.
Mit 5 Abbildungen und 1 Tabelle 相似文献
Summary An ultracentrifugal study of the sedimentation equilibrium of the system Na2[H2W12O40]-NaClO4-H2Oat 25 °C is presented. The dependency of the apparent charge of the sodium metatungstate on NaClO4-molality is investigated. From these data the dissociation constant for the dissociation of the sodium metatungstate in the presence of NaClO4 according to the equationNa[H2W12O40] 6Na+ + [H2W12O40]6– is calculated toK=0.08 mol6·kg–6. The cross differential quotient ( PXz is the trace activity coefficient of the sodium metatungstate) shows a behavior in its dependence on NaClO4-molality which to our knowledge has not yet been reported by other authors.
Mit 5 Abbildungen und 1 Tabelle 相似文献
9.
Kremser L Brückner A Heger A Grunert T Buchacher A Josic D Allmaier G Rizzi A 《Electrophoresis》2003,24(24):4282-4290
The isoforms distribution of the glycoprotein antithrombin III (ATIII) derived from human plasma was investigated by means of isoelectric focusing (IEF) in polyacrylamide gels with immobilized pH gradients (IPG) and two-dimensional gel electrophoresis (2-DE) as well as capillary electrophoretic methods. It turned out that the presence of high concentrations of chaotropics (urea, thiourea) and zwitterionic detergents (3-[(3-cholamidepropyl)dimethylammonio]-1-propanesulfonate (CHAPS)) was decisive for attaining good resolution of the protein isoforms. Resolution by IPG-IEF was obtained with excellent reproducibility and pI differences down to 0.01 pH units could be distinguished. ATIII-alpha and ATIII-beta-fractions preseparated by heparin affinity chromatography showed an analogous but shifted spot pattern consisting each of one major and three minor isoforms. The main isoforms of ATIII-alpha and ATIII-beta exhibit pI values of 5.18 and 5.32, respectively, both values determined in the presence of high concentrations of urea. The pI difference of 0.14 pH units correspond to the effect of two sialic acids absent in ATIII-beta. The formation and occurrence of ATIII dimers and trimers turned out to be dependent on the sample preparation. The results obtained by 2-DE were compared with those of capillary zone electrophoresis (CZE) and capillary IEF (CIEF). Quantitative analysis regarding the CZE separated isoforms of plasma derived ATIII yielded a content of about 70% ATIII-alpha main isoform and about 6.6% of ATIII-beta. The pI values of ATIII determined by CIEF with internal calibration were in fair agreement with the pI values of the main isoforms achieved with 2-DE. 相似文献
10.
Reaction of Telluriumhexafluoride and Trimethylamine, Structures of the TeF5? and SeF5? Anions The reaction of TeF6 and (CH3)3N is of the redox kind, resulting in reduction of tellurium: X-ray single crystal analysis reveals the compounds (CH3)2N? CH2? N(CH3)2+TeF5? and [(CH3)3NH+]5(TeF5?)3(HF2?)2. By comparison with published data it can be shown that this mixture is identical to previously published [(CH3)3N]2TeF6. The latter was supposed to be one of the few examples of tellurium in a coordination state of eight. (CH3)4N+TeF5? and (CH3)4N4SeF5? are obtained and their structure is investigated by single crystal x-ray methods also. The anions SF5?, SeF5? and TeF5? are discussed in terms of weak interactions. 相似文献