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排序方式: 共有671条查询结果,搜索用时 390 毫秒
31.
Vladislav Oliva Jaroslav Vclavík Ale Materna Patrick Lorenzetto Andreas Furmanek 《Fusion Engineering and Design》2009,84(7-11):1450-1454
An objective of experiments and finite element simulations was to check the stiffness, the strength and the fatigue resistance of the attachment of the First Wall panels onto a shield block of blanket modules according to the ITER 2001 design. The panel has a poloidal key at the rear side (in so-called option A with the rear access bolting) and it is attached by means of special studs located on a key-way in the shield block. Special device for a test of stud tensile pre-load relaxation during a thermal cycling was developed. True-to-scale panels, the shield block mock-up and simplified studs were fabricated and the assembly was loaded alternatively by radial moment, poloidal force or poloidal moment simulating the loading during off-normal plasma operations. Thermal cycling led to an acceptable stud pre-load relaxation. Mechanical cycling caused neither the pre-load relaxation nor the loss of the contact in the key-way nor a damage of the attachment system. The combination of poloidal moment and radial force during vertical displacement events (VDEs) seems to be a most dangerous case because it could lead to the loss of the key–key-way contact. 相似文献
32.
Application of the Electrodiffusion Method to Measure Wall Shear Stress: Integrating Theory and Practice 下载免费PDF全文
Lutz Böhm Sepideh Jankhah Jaroslav Tihon Pierre R. Bérubé Matthias Kraume 《化学工程与技术》2014,37(6):938-950
The electrodiffusion method has been used in fluid dynamic research for the past 50 years. It allows the measurement of wall shear stress, a crucial parameter, e.g., for the cleaning of membrane modules used in water filtration. Various authors have published articles dealing with the theory behind this technique. But no paper collects all the knowledge assembled over five decades of application. Here, comprehensive summary of the theory of steady flow, unsteady flow, and transient voltage step experiments is given. Factors influencing the accuracy of the measurements are discussed. Furthermore, a new approach to calibrate the system from voltage step experiments is introduced, and practical issues related to its application in flow measurements are discussed for an exemplary signal response to a near‐wall flow. 相似文献
33.
Thin composite layers (tin in plasma polymer matrix) were prepared in a stainless steel vacuum chamber. An RF powered magnetron with tin target was used to excite the discharge and to activate the monomer species (n-hexane). The gas mixture introduced comprised Ar and n-hexane vapours. The properties of the films and chemical composition were characterized by AFM (surface morphology), TEM and Electron tomography (bulk structure characterization), XPS and FTIR spectroscopy (chemical composition analyses). Current-voltage characteristics were measured to examine the electrical properties of the layers and their dependence on the deposition parameters. 相似文献
34.
The complexation of charged compounds by humic acids represents the process of exceptional environmental importance. Nevertheless, traditional methods utilized in the complexation studies do not address the way, how these interactions affect the transport of ions in humic-rich environments. To overcome this dilemma, the diffusion cells technique is proposed as an innovative reactivity mapping technique. Using this method, the diffusion of methylene blue was studied in aqueous solutions and in agarose gels with and without the addition of humic acids. Experimental results clearly illustrate the immobilizing effects of humic acids on the transport of methylene blue in gels. The partitioning of methylene blue at the solution-gel interface and the specific interactions between methylene blue and humic acids is discussed on the basis of experimental data. Effective structural parameters of hydrogels (effective porosity, tortuosity factor) were calculated, as well as some standard diffusion and interaction parameters (diffusion and partition coefficients and apparent equilibrium constants). 相似文献
35.
Jaroslav Stejskal Miroslava Trchová Jir̆ina Hromádková Jana Kovár̆ová Andrea Kalendová 《Polymer International》2010,59(7):875-878
The carbonization of nanostructures afforded by conducting polymers represents a new route to the preparation of functional nanostructured carbons. The exposure of colloidal polyaniline particles stabilized with poly(N‐vinylpyrrolidone) or silica nanoparticles at 650 °C in inert atmosphere led, in both cases, to nitrogen‐containing carbonaceous materials with specific surface areas of 200 and 205 m2 g?1, respectively, and conductivities of 8.3 × 10?7 and 1.9 × 10?10 S cm?1, respectively. The latter material contained 77 wt% of silica. The original particulate nanostructure of the samples was preserved after carbonization. The carbon‐to‐nitrogen atomic ratio was 7.2 and 7.9; the nitrogen content in the carbonized polyaniline–poly(N‐vinylpyrrolidone) particles was 10.8 wt%. Thermogravimetric analysis in air revealed their stability to be up to 500 °C. This is comparable with commercial multi‐wall carbon nanotubes, which have similar areas of application. The nitrogen‐containing carbons are potentially useful as supports for catalysts and in applications where carbon of higher hydrophilicity would be of benefit. Copyright © 2010 Society of Chemical Industry 相似文献
36.
Mária Omastová Katarína Mosnáčková Miroslava Trchová Elena N. Konyushenko Jaroslav Stejskal Pavol Fedorko Jan Prokeš 《Synthetic Metals》2010,160(7-8):701-707
The conducting polymers, polypyrrole and polyaniline, were synthesized by chemical oxidative polymerization of the corresponding monomers in 0.1 M sulfuric acid using cerium(IV) sulfate as the oxidant at mole ratios of oxidant-to-monomer ranging from 0.5 to 3. The yields of the oxidation products were determined, and the samples were characterized with respect to their elemental composition, molecular structure, and morphology. The conductivity of polypyrrole prepared in 0.1 M sulfuric acid, 10?1 to 100 S cm?1, was higher compared with the conductivity of polyaniline prepared under the same conditions, 10?3 to 10?1 S cm?1. The loss of mass after deprotonation with ammonium hydroxide is reported, and discussed in terms of the type of protonation as also reflected by FTIR spectroscopy. The conductivity of polypyrrole bases remained at relatively high level, 10?5 to 10?3 S cm?1, while PANI bases became non-conducting, 10?12 to 10?10 S cm?1. The polymers had a granular morphology in all cases. 相似文献
37.
Partition coefficients of phenol, salicylic acid, and several environmentally important chloro- and nitrophenols in a supercritical CO2-water system were measured using direct cocurrent extraction of aqueous solutions of the individual solutes with CO2. Partitioning data on the nitrophenols and salicylic acid were obtained for the first time. To bypass the troublesome and error-prone analysis of the CO2-rich phase, the present method employed only the solute concentrations in the aqueous phase before and after extraction to determine the partition coefficient. Unlike most previous engineering studies of phenol partitioning in a CO2-water system, the concentrations of phenolic solutes approached infinite dilution in both phases. This makes the results relevant to analytical-scale SFE of environmental water samples with CO2. Because of effective infinite dilution of the solutes, the partition coefficients provide a direct measure of relative CO2-philicity/hydrophilicity of the individual phenols. Compared to the octanol-water partition coefficients of substituted phenols, the CO2-water partition coefficients are more sensitive to substitution in the position neighboring the hydroxyl group. 相似文献
38.
Jaroslav Kautsky Jan Flusser Barbara Zitov Stanislava
imberov 《Pattern recognition letters》2002,23(14):1785-1794
We present a new measure of image focus. It is based on wavelet transform of the image and is defined as a ratio of high-pass band and low-pass band norms. We show this measure is monotonic with respect to the degree of defocusation and sufficiently robust. We experimentally illustrate its performance on simulated as well as real data and compare it with existing focus measures (gray-level variance and energy of Laplacian). Finally, an application of the new measure in astronomical imaging is shown. 相似文献
39.
Analysis of the reaction mechanism and substrate specificity of haloalkane dehalogenases by sequential and structural comparisons 总被引:1,自引:0,他引:1
Haloalkane dehalogenases catalyse environmentally importantdehalogenation reactions. These microbial enzymes representobjects of interest for protein engineering studies, attemptingto improve their catalytic efficiency or broaden their substratespecificity towards environmental pollutants. This paper presentsthe results of a comparative study of haloalkane dehalogenasesoriginating from different organisms. Protein sequences andthe models of tertiary structures of haloalkane dehalogenaseswere compared to investigate the protein fold, reaction mechanismand substrate specificity of these enzymes. Haloalkane dehalogenasescontain the structural motifs of /ß-hydrolases and epoxidaseswithin their sequences. They contain a catalytic triad withtwo different topological arrangements. The presence of a structurallyconserved oxyanion hole suggests the two-step reaction mechanismpreviously described for haloalkane dehalogenase from Xanthobacterautotrophicus GJ10. The differences in substrate specificityof haloalkane dehalogenases originating from different speciesmight be related to the size and geometry of an active siteand its entrance and the efficiency of the transition stateand halide ion stabilization by active site residues. Structurallyconserved motifs identified within the sequences can be usedfor the design of specific primers for the experimental screeningof haloalkane dehalogenases. Those amino acids which were predictedto be functionally important represent possible targets forfuture site-directed mutagenesis experiments. 相似文献
40.
Jaroslav Barto 《Polymer International》1993,30(2):151-156
Conversion curves have been determined at 60°C for the polymerization of acrylamide in percolating inverse microemulsions. Ammonium peroxo-disulphate (APS) and dibenzoyl peroxide (DBP) were used as initiators of free-radical polymerization in the presence or absence of potassium nitrosodisulphonate (Fremy's salt, FS). The percolation decreases the rate of polymerization of acrylamide initiated by APS. The polymerization is inhibited by FS. After an inhibition period, retardation of acrylamide polymerization is more pronounced in non-percolating microemulsions. No inhibition periods were observed for DBP-initiated polymerization of acrylamide. The percolation shortens the time interval of the ‘slow’ polymerization of acrylamide, but the rates of rapid acrylamide polymerization above 10% conversion are the same for percolating and for non-percolating inverse microemulsions. The polymer particle diameter is a function of acrylamide/water weight ratio and of [water]/[AOT] (AOT: bis(2-ethylhexyl)-sulphosuccinate sodium salt) molar ratio. No effect of the initiator's nature either in the presence or in the absence of FS was found. The results are interpreted on the basis of initiator and/or nitroxide radical partitioning between oil and water phases of the inverse microemulsion, and are discussed with respect to the mechanism of acrylamide polymerization and polymer particle formation proposed for non-percolating inverse microemulsions. 相似文献