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991.
This paper presents the probabilistic analysis of concrete-faced rockfill (CFR) dams according to the Monte Carlo Simulation (MCS) results which are obtained through the Response Surface Method (RSM). ANSYS finite element program is used to get displacement and principal stress components. First of all, some parametric studies are performed according to the simple and representative finite element model of dam body to obtain the optimum approximate model. Secondly, a sensitivity analysis is performed to get the most effective parameters on dam response. Then, RSM is used to obtain the approximate function through the selected parameters. After the performed analyses, star experimental design with quadratic function without mixed terms according to the k = 1 is determined as the most appropriate model. Finally, dam-foundation-reservoir interaction finite element model is constituted and probabilistic analyses are performed with MCS using the selected parameters, sampling method, function and arbitrary factor under gravity load for empty and full reservoir conditions. Geometrically and materially nonlinearity are considered in the analysis of dam-foundation-reservoir interaction system. Reservoir water is modeled by fluid finite elements based on the Lagrangian approach. Structural connections are modeled as welded contact and friction contact based on Coulomb’s friction law. Probabilistic displacements and stresses are presented and compared with deterministic results. 相似文献
992.
Finite element analysis has become an essential tool to estimate structural responses under static and dynamic loads. However, there are a lot of uncertainties in structural properties. For this reason, in many cases, the outcomes of the theoretical and experimental modal analyses do not match. Therefore, the analytical models of the structures need to be updated according to the experimental test results. The commonly used method to get parameters for model updating is experimental modal analysis which provides structural dynamic characteristic (natural frequencies, mode shapes and modal damping ratio). There are many methods available for the updating process. This study addresses an updating algorithm to modify the numerical models by using the design points for unknown structural properties. The proposed method aims to minimize the difference between the analytical and experimental natural frequencies by updating uncertain parameters for each mode and combine them to get an optimum solution. The algorithm is tested on a column and a 2D frame models. These models are investigated by taking the connection rigidity and elasticity modulus as unknown parameters. It is observed that the proposed algorithm gives better results for unknown structural properties compared to the initial values. 相似文献
993.
994.
We report on the electrochemical behaviour and electropolymerization of self‐assembled monolayers (SAMs) of methylene blue (MB) on gold electrodes. The SAMs of MB on gold electrodes were prepared by immersing the substrates into a solution of 1.0 mM MB in absolute ethanol for different times at room temperature. Cyclic voltammetry experiments exhibited that reductive desorption of MB monolayer takes place at three different potentials on polycrystalline gold electrodes, while reductive desorption of MB monolayer consists of only one peak on single crystal Au(111) substrates. Calculated charge densities for different immersion times indicated that optimal immersion time for self‐assembly of MB is 96 h. Electropolymerization of SAMs of MB on gold electrode was achieved by applying 0.95 V for 1 s in 0.1 M borate buffer solution (pH: 9.0). It was observed that poly(MB) monolayers are highly stable in acidic media. ATR‐FTIR and UV‐vis spectra exhibited differences between monomer and polymer monolayers, which are attributed to surface‐confined electropolymerization. STM image of poly(MB) monolayer on Au(111) substrate revealed a surface that is covered by well‐ordered, collateral nanowires with an average size of 3 nm. 相似文献
995.
In this study, a series of ultraviolet (UV)‐curable organic–inorganic hybrid coating materials containing phosphorus were prepared by sol–gel approach from acrylate end‐capped urethane resin, acrylated phenyl phosphine oxide oligomer (APPO), and inorganic precursors. TEOS and MAPTMS were used to obtain the silica network and Ti:acac complex was employed for the formation of the titania network in the hybrid coating systems. Coating performance of the hybrid coating materials applied on aluminum substrates was determined by the analysis techniques, such as hardness, gloss, impact strength, cross‐cut adhesion, taber abrasion resistance, which were accepted by international organization. Also, stress–strain test of the hybrids was carried out on the free films. These measurements showed that all the properties of the hybrids were enhanced effectively by gradual increase in sol–gel precursors and APPO oligomer content. The thermal behavior of the hybrid coatings was investigated by thermogravimetric analysis (TGA) analysis. The flame retardancy of the hybrid materials was examined by the limiting oxygen index (LOI); the LOI values of pure organic coating (BF) increased from 31 to 44 for the hybrid materials containing phosphorus (BF‐P:40/Si:10). The data from thermal analysis and LOI showed that the hybrid coating materials containing phosphorus have higher thermal stability and flame resistance properties than the organic polymer. Besides that, it was found that the double bond conversion values for the hybrid mixtures were adequate in order to form an organic matrix. The polycondensation reactions of TEOS and MAPTMS compounds were also investigated by 29Si‐NMR spectroscopy. SEM studies of the hybrid coatings showed that silica/titania particles were homogenously dispersed through the organic matrix. In addition, it was determined that the hybrid material containing phosphorus and silica showed fibrillar structure. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
996.
The functions of nanoclay and three different boron containing substances, zinc borate (ZnB), borophosphate (BPO4), and boron silicon containing preceramic oligomer (BSi), were studied to improve the flame retardancy of polypropylene (PP)‐nanoclay‐intumescent system composed of ammonium polyphosphate (APP) and pentaerythritol (PER). The flame retardancy of PP composites was investigated using limiting oxygen index (LOI), UL‐94 standard, thermogravimetric analysis (TGA), and cone calorimeter. According to the results obtained, the addition of 20 wt% intumescent flame retardant (IFR) improved the flame retardancy by increasing the char formation. Addition of clay slightly increases the LOI value and reduces the maximum heat release rate (HRR). Addition of clay also increases the barrier effect due to intumescent char, especially in thin samples. Boron compounds show their highest synergistic effect at about 3 wt% loading. According to UL‐94 test and LOI test, 3 wt% ZnB containing composite shows the highest rating (V0) and BPO4 containing sample shows the highest LOI value (26.5). Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
997.
Diphasic gels prepared by mixing freshly prepared polymeric silica and polymeric boehmite sols through a modified Al-alkoxide
route in mullite compositions led to the crystallization of mullite upon heat treatment at 775 °C. Mullite formation was observed
at a 100 °C higher temperature when diphasic gels were formed by mixing aged polymeric sols containing about 2 nm in diameter
boehmite species. These relatively low mullite formation temperatures were attributed to the nanoscale sizes of the polymeric
species of the two amorphous phases present in the diphasic gels. 相似文献
998.
999.
In this paper, we prove that every metric line of a Möbius gyrovector space ${(\mathbb{R}_{1}^{n}, \oplus, \otimes)}$ is exactly a cogyroline of itself, and also we prove the nonexistence of periodic lines in ${(\mathbb{R}_{1}^{n}, \oplus, \otimes)}$ . 相似文献
1000.
The synthesis of diblock copolymers of poly(N-isopropylacrylamide) (PNIPAM) and poly(vinyl acetate) (PVAc) was performed by macromolecular design via interchange of xanthates (MADIX) process. Following the preparation of methyl (isopropoxycarbonothioyl) sulfanyl acetate (MIPCTSA) as chain transfer agent, it was reacted with vinyl acetate to obtain PVAc macro-chain transfer agent. Then, block copolymerization was completed by successive addition of N-isopropylacrylamide (NIPAM). 1H NMR spectroscopy confirmed the presence of both blocks in the copolymer structure, with the expected composition based on the feed ratio. Size Exclusion Chromatography (SEC) was used to investigate the relative values of molecular characteristics. Only 20% of PVAc was converted to block copolymer. The resultant block copolymer structures were further examined in terms of their morphologies as well as critical micelle concentration (CMC) by using ESEM and Fluorescence Excitation Spectroscopic techniques, respectively. Morphological characterization confirmed amphiphilic block copolymer formation with the existence of mainly ca. 100 nm well distributed micelles. The thermo responsive amphiphilic behavior of the block copolymer solutions were followed by Dynamic Light Scattering (DLS) technique. 相似文献