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31.
A finite difference scheme with fourth order Runge-Kutta method is employed to determine the unsteady state temperature distribution in a plane slab with uniform heat generation. The plane slab is insulated on one face and subjected to convective and radiative cooling at the other face. The plane slab has a uniform initial temperature and the ambient environment as well as the fluid temperatures are assumed to be constant. Heat conduction is considered to be one dimensional. Results are presented in dimensionless charts over a wide range of parameters.
Nomenclature Bi Biot number - c specific heat - h heat transfer coefficient - k thermal conductivity - L half thickness of plate - Nr Radiation number - T absolute temperature - t time - F o dimensionless time - T e environment temperature - T f fluid temperature - T i initial plate temperature - u internal energy generation number - u internal energy generation - x space coordinate - x* dimensionless space coordinate Greek symbols thermal diffusivity - emissivity - dimensionless temperature - density - Stephan-Boltzman constant 相似文献
Instationäre Wärmeleitung mit gleichförmiger Wärmeerzeugung in einer Platte bei Kühlung durch Konvektion und Abstrahlung
Zusammenfassung Zur Ermittlung der instationären Temperaturverteilung in einer Platte mit gleichförmiger Wärmeerzeugung wird ein Differenzverfahren vierter Ordnung nach Runge-Kutta angewendet. Die ebene Platte ist einseitig isoliert und wird auf der anderen Seite durch Konvektion und Abstrahlung gekühlt. Zu Beginn befindet sich die Platte gleichförmig auf einer bestimmten Anfangstemperatur, die Temperaturen der umgebenden Objekte sowie des Fluids sind ebenfalls konstant. Der Wärmeleitungsvorgang sei eindimensional. Die Ergebnisse sind in dimensionsloser Form für einen weiten Parameterbereich in Diagrammform dargestellt.
Nomenclature Bi Biot number - c specific heat - h heat transfer coefficient - k thermal conductivity - L half thickness of plate - Nr Radiation number - T absolute temperature - t time - F o dimensionless time - T e environment temperature - T f fluid temperature - T i initial plate temperature - u internal energy generation number - u internal energy generation - x space coordinate - x* dimensionless space coordinate Greek symbols thermal diffusivity - emissivity - dimensionless temperature - density - Stephan-Boltzman constant 相似文献
32.
Bai R Nguyen TL Burnett JC Atasoylu O Munro MH Pettit GR Smith AB Gussio R Hamel E 《Journal of chemical information and modeling》2011,51(6):1393-1404
Compounds that modulate microtubule dynamics include highly effective anticancer drugs, leading to continuing efforts to identify new agents and improve the activity of established ones. Here, we demonstrate that [(3)H]-labeled halichondrin B (HB), a complex, sponge-derived natural product, is bound to and dissociated from tubulin rapidly at one binding site per αβ-heterodimer, with an apparent K(d) of 0.31 μM. We found no HB-induced aggregation of tubulin by high-performance liquid chromatography, even following column equilibration with HB. Binding of [(3)H]HB was competitively inhibited by a newly approved clinical agent, the truncated HB analogue eribulin (apparent K(i), 0.80 μM) and noncompetitively by dolastatin 10 and vincristine (apparent K(i)'s, 0.35 and 5.4 μM, respectively). Our earlier studies demonstrated that HB inhibits nucleotide exchange on β-tubulin, and this, together with the results presented here, indicated the HB site is located on β-tubulin. Using molecular dynamics simulations, we determined complementary conformations of HB and β-tubulin that delineated in atomic detail binding interactions of HB with only β-tubulin, with no involvement of the α-subunit in the binding interaction. Moreover, the HB model served as a template for an eribulin binding model that furthered our understanding of the properties of eribulin as a drug. Overall, these results established a mechanistic basis for the antimitotic activity of the halichondrin class of compounds. 相似文献
33.
Smith AB Risatti CA Atasoylu O Bennett CS Liu J Cheng H TenDyke K Xu Q 《Journal of the American Chemical Society》2011,133(35):14042-14053
The design, synthesis, and biological evaluation of two diminutive forms of (+)-spongistatin 1, in conjunction with the development of a potentially general design strategy to simplify highly flexible macrocyclic molecules while maintaining biological activity, have been achieved. Examination of the solution conformations of (+)-spongistatin 1 revealed a common conformational preference along the western perimeter comprising the ABEF rings. Exploiting the hypothesis that the small-molecule recognition/binding domains are likely to comprise the conformationally less mobile portions of a ligand led to the design of analogues, incorporating tethers (blue) in place of the CD and the ABCD components of the (+)-spongistatin 1 macrolide, such that the conformation of the retained (+)-spongistatin 1 skeleton would mimic the assigned solution conformations of the natural product. The observed nanomolar cytotoxicity and microtubule destabilizing activity of the ABEF analogue provide support for both the assigned solution conformation of (+)-spongistatin 1 and the validity of the design strategy. 相似文献
34.
Michael J. Patrick Chia-Yuan Chen David H. Frakes Onur Dur Kerem Pekkan 《Experiments in fluids》2011,50(4):887-904
In hemodynamics, the inherent intermittency of two-phase cellular-level flow has received little attention. Unsteadiness is
reported and quantified for the first time in the literature using a combination of fluorescent dye labeling, time-resolved
scanning confocal microscopy, and micro-particle image velocimetry (μPIV). The near-wall red blood cell (RBC) motion of physiologic
high-hematocrit blood in a rectangular microchannel was investigated under pressure-driven flow. Intermittent flow was associated
with (1) the stretching of RBCs as they passed through RBC clusters with twisting motions; (2) external flow through local
obstacles; and (3) transitionary rouleaux formations. Velocity profiles are presented for these cases. Unsteady flow clustered
in local regions. Extra-cellular fluid flow generated by individual RBCs was examined using submicron fluorescent microspheres.
The capabilities of confocal μPIV post-processing were verified using synthetic raw PIV data for validation. Cellular interactions
and oscillating velocity profiles are presented, and 3D data are made available for computational model validation. 相似文献
35.
Onur ahin Orhan Büyükgüngr Dursun Ali Kse Hacali Necefoglu 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(11):m510-m512
The title compound, [Cu(C7H5O3)2(C6H6N2O)2(H2O)2], is a two‐dimensional hydrogen‐bonded supramolecular complex. The CuII ion resides on a centre of symmetry and is in an octahedral coordination environment comprising two pyridine N atoms, two carboxylate O atoms and two O atoms from water molecules. Intermolecular N—H...O and O—H...O hydrogen bonds produce R22(4), R22(8) and R22(15) rings which lead to one‐dimensional polymeric chains. An extensive two‐dimensional network of N—H...O and O—H...O hydrogen bonds and C—H...π interactions are responsible for crystal stabilization. 相似文献
36.
We introduce a "double direct templating" method for obtaining hollow microspheres with periodically nanostructured walls. Silica or polystyrene colloids are dispersed in a self-assembled hexagonal lyotropic liquid crystal containing precursors for ZnS. The semiconductor ZnS mineralizes on the surface of the colloid, expressing a pore morphology that is a copy of the structure of the liquid crystal. After etching of the sacrificial colloids, hollow capsules with templated and uniform mesoporous shells are obtained. 相似文献
37.
38.
Dağlı Özge Köse Dursun Ali İçten Okan Avcı Gülçin Alp Şahin Onur 《Journal of Thermal Analysis and Calorimetry》2019,136(4):1467-1480
Journal of Thermal Analysis and Calorimetry - The coumarilate (coum?) and 1,10-phenanthroline (phen) mixed ligand complexes of Co(II) (1), Ni(II) (2) Cu(II) (3) and Zn(II) (4) were... 相似文献
39.
We demonstrate a technique for characterizing two-photon quantum states based on joint temporal correlation measurements using time-resolved single-photon detection by femtosecond up-conversion. We measure for the first time the joint temporal density of a two-photon entangled state, showing clearly the time anticorrelation of the coincident-frequency entangled photon pair generated by ultrafast spontaneous parametric down-conversion under extended phase-matching conditions. The new technique enables us to manipulate the frequency entanglement by varying the down-conversion pump bandwidth to produce a nearly unentangled two-photon state that is expected to yield a heralded single-photon state with a purity of 0.88. The time-domain correlation technique complements existing frequency-domain measurement methods for a more complete characterization of photonic entanglement. 相似文献
40.
Five new metal complexes [Pd(LH)2] (1), [Pd(L)2Ru2(bpy)4](ClO4)2 (2), [Pd(L)2Ru2(phen)4](ClO4)2 (3), [Pd(L)2Ru2(dafo)4](ClO4)2 (4) and [Pd(L)2Ru2(dcbpy)4](ClO4)2 (5), (where, L = ligand, bpy = 2,2′-bipyridine, phen = 1,10-phenantroline, dafo = 4,5-diazafluoren-9-one and dcbpy = 3,3′-dicarboxy-2,2′-bipyridine) have been isolated and characterized by UV-VIS, FT-IR, 1H NMR, magnetic susceptibility measurements, elemental analysis, molar conductivity, X-ray powder techniques, thermal analyses and their morphology studied by SEM measurements. IR spectra show that the ligand acts in a tetradentate manner and coordinates N4 donor groups of LH2 to PdII ion. The disappereance of H-bonding (O−H···O) in the trinuclear RuII-PdII-RuII metal complexes, the RuII ion centered into the main oxime core by the coordination of the imino groups while the two RuII ions coordinate dianionic oxygen donors of the oxime groups and linked to the ligands of bpy, phen, dafo and dbpy. The X-powder results show that 1 metal complex is indicating crystalline nature, not amorphous nature. Whereas, the X-ray powder pattern of the ligand (LH2) with 2, 3,4 and 5 exhibited only broad humps, indicating its amorphous nature. The catalytic activity of three different complexes were tested in the Suzuki coupling reaction. The 1, 4 and 5 metal complexes catalyse Suzuki coupling reaction between phenylboronic acid and arylbromides affording biphenyls. Also, the thermal results shown that the most stable complex is 1 compound while the less stable is 4 compound. 相似文献