Characterization of Trimmed NURBS Surface Boundaries Using Topological Criteria

This paper presents an approach based on topology for the determination of characteristics and properties of curves used in the trimming of NURBS surfaces. Through discrete subdivision and topological criteria, a method is presented to determine characteristics of the boundary; such as whether the set of trimming curves forms a set of closed loops, whether trimming curves contain singularities or self intersections, and whether the boundary is simply connected. A surface mesh partitionning the parameter space is used, formed of isoparametric lines in both parametric directions. Topological properties of the cells of this mesh and their intersections with the trimming curves allow to localize the boundary. Topological treatment of this localization allows to define the interior and exterior of the face, and to refine the boundary localization. Singularities and self intersections of the boundary as well as voids in the face are investigated through the study of topological properties of neighbors. As an application, an algorithm for point localization is presented that very rapidly allows to determine whether a given point in parameter space lies inside, on the boundary or outside of the trimmed surface.     

A combined experimental and DFT investigation of the adsorption of humic acid by-products on polypyrrole

This study sheds light on the removal of humic acid by-products (trimellitic and pyromellitic acids; TMA and PMA, respectively) from aqueous solution using conducting polypyrrole (PPy) as an effective adsorbent. The effects of experimental factors including contact time, solution pH, initial concentration, adsorbent dose, and temperature were systematically investigated. The pseudo-second-order kinetic model provides the best correlation with adsorption experimental data. The equilibrium adsorption was well described by the Langmuir model with maximum mono-layer adsorption capacities of 47.62 and 71.43?mg?g^?1 for TMA and PMA, respectively. The analysis of thermodynamic parameters indicated that the adsorption process was spontaneous and endothermic in nature. In addition, we investigated the adsorption mechanism using the density functional theory (DFT) calculations. The TMA and PMA were physisorbed on the PPy surface through the formation of hydrogen bonds between carboxylic groups of adsorbate molecules and the amino group of the adsorbent. The calculated theoretical data were in good agreement with experiments.     

Optimization of process parameters and its effect on structure and morphology of CuO nanoparticle synthesized via the sol−gel technique

This article describes systematic basic research on the optimization of the processing parameters of sol?gel technique for synthesis of the high purity CuO nanoparticles. Effect of the synthesis parameters such as copper salt concentration, solvent and gelating agent, optimized one at a time, was investigated by employing XRD, TEM, FESEM, micro-Raman, UV-visible-NIR and PL spectroscopies. XRD results clearly demonstrate the monoclinic structure of CuO nanoparticles with traceable impurities at a lower molar concentration of Cu²⁺, transition of nucleation system from homogeneous to heterogeneous state with the increase in concentration of Cu²⁺ from 0.05 to 0.15?M. It was also found that the isopropyl alcohol offers better results in comparison to ethanol and water. Moreover, the lattice parameters, space group, and crystal system were determined by powder X-ray diffraction method. Further we propose the optimization of synthesis process using ethylene glycol and citric acid (EG:CA). The Raman analysis confirmed the influence of ethylene glycol and citric acid ratio and TEM observations confirmed that EG:CA 1:2 ratio formulate homogenous flower-like nanostructures. The optical absorption of CuO nanostructures can be easily tuned by varying the concentration of citric acid without changing other conditions; it shows the role of synthesis parameters more significant. Our results suggest that the prepared CuO nanostructures have a potential to be used as absorbing material in solar cell applications.

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PVP Assisted Shape-Controlled Synthesis of Self-Assembled 1D ZnO and 3D CuO Nanostructures

Self-assembled one-dimensional (1D) zinc oxide (ZnO) rods and three-dimensional (3D) cupric oxide (CuO) cubes like nanostructures with a mean crystallite size of approximately 33 and 32 nm were synthesized through chemical route in the presence of polyvinylpyrrolidone (PVP) under mild synthesis conditions. The technique used for the synthesis of nanoparticles seems to be an efficient, inexpensive and easy method. X-Ray diffraction patterns confirmed well crystallinity and phase purity of the as prepared samples, followed by the compositional investigation using Fourier Transform Infrared (FT-IR) spectroscopy. The formation of ZnO nanorods and CuO nanocubes like structures were through Scanning Electron Microscopy (SEM) images. The mechanism and the formation factors of the self-assembly were discussed in detail. It was clearly observed from results that the concentration of precursors and PVP were important factors in the synthesis of self-assembly ZnO and CuO nanostructures. These self-assembly nanostructures maybe used as novel materials in various potential applications.     

Relaxation of variational problems in two-dimensional nonlinear elasticity

Consider a plate occupying in a reference configuration a bounded open set Ω ⊂ ℝ ² , and let be its stored-energy function. In this paper we are concerned with relaxation of variational problems of type:

Homogenization of unbounded singular integrals in W 1,∞

We study homogenization by ??-convergence, with respect to the L ¹-strong convergence, of periodic multiple integrals in W ^1,?? when the integrand can take infinite values outside of a convex bounded open set of matrices.     

Electrochemical biosensing of DNA hybridization by ferrocenyl groups functionalized polypyrrole

We have developed a new material based on polypyrrole functionalized with both ferrocenyl group and DNA probe. We have developed a precursor polymer based on a pyrrole 3-acetic acid and a pyrrole bearing ferrocenyl groups substituted by easy leaving group in which amino-labeled oligonocleotides probe were directly linked. The electrochemical response of the modified electrode was examined both in aqueous and organic media and shows high electroactivity in both media. A large modification of redox activity of ferrocenyl groups was obtained upon addition of ODN target to the electrolytic media, which is determined by amperometric methods. The detection limit of this electrochemical biosensor is about 10⁻¹⁴ mol without any signal processing.     

Combined parametric optimization of P3HT: PC70BM films for efficient bulk-heterojunction solar cells

Journal of Solid State Electrochemistry - In this report, the effects of photoactive blend compositions, film thicknesses, and annealing conditions on the P3HT:PC70BM solar cells performance and...     

A novel and simplified procedure for patterning hydrophobic and hydrophilic SAMs for microfluidic devices by using UV photolithography

This work describes how selective patterning of hydrophobic and hydrophilic areas inside microchannels of microfluidic devices can be achieved by combining well-known chemical protocols and standard photolithography equipment (365 nm). Two techniques have been performed and compared. The first technique is based on the preparation of self-assembled monolayers of photocleavable organosilane and the second one on photoassisted grafting (365 nm) of self-assembled monolayers (SAMs) on a silicon or glass substrate. In the first case, we begin with monolayers carrying an o-nitrobenzyl function (hydrophobic area) that is photochemically cleaved, revealing a carboxylic acid group (hydrophilic area). The problem is that the energy necessary to cleave this monolayer is too high and the reaction time is more than 1 h with 50 mW/cm(2) irradiation flux. To overcome this practical disadvantage, we propose another approach that is based on the thiol-ene reaction with benzophenone as photoinitiator. In this approach, a monolayer of mercaptopropyltrimethoxysilane (MPTS) is prepared first. Subsequently, a hydrocarbon chain is photografted locally onto the thiol layer, forming a hydrophobic surface while the reminding unmodified thiol surface is oxidized into sulfonic acid (hydrophilic area). We demonstrated the feasibility of this approach and synthesized high-quality self-assembled monolayers by UV grafting with an irradiation time of 30 s at 365 nm (50 mW/cm(2)). The modified surfaces have been characterized by contact angle measurements, X-ray photoelectron spectroscopy (XPS), AFM, and multiple internal reflection infrared spectroscopy (MIR-FTIR). The difference in the contact angles on the hydrophilic and hydrophobic surfaces reached a remarkable 77 degrees. We have also demonstrated that this method is compatible with selective surface grafting inside microfluidic channels.