Plastic analysis of concrete containment structure

Overpressure capacity of a box type concrete containment structure is evaluated. Plastic analysis of the finite element model is performed using a quadrilateral plate element of homogeneous material. A special approach is used to represent nonlinear properties of reinforced concrete, such as concrete cracking and crushing and steel yielding. Those properties are represented by a set of idealized stress-strain curves of equivalent homogeneous sections.The analysis allows for a better estimate of the overpressure capacity of the containment structure while keeping the computer cost low by avoiding the use of the more expensive reinforced concrete brick element.     

dOCAL: high-level distributed programming with OpenCL and CUDA

In the state-of-the-art parallel programming approaches OpenCL and CUDA, so-called host code is required for program’s execution. Efficiently implementing host code is often a cumbersome task, especially when executing OpenCL and CUDA programs on systems with multiple nodes, each comprising different devices, e.g., multi-core CPU and graphics processing units; the programmer is responsible for explicitly managing node’s and device’s memory, synchronizing computations with data transfers between devices of potentially different nodes and for optimizing data transfers between devices’ memories and nodes’ main memories, e.g., by using pinned main memory for accelerating data transfers and overlapping the transfers with computations. We develop distributed OpenCL/CUDA abstraction layer (dOCAL)—a novel high-level C++ library that simplifies the development of host code. dOCAL combines major advantages over the state-of-the-art high-level approaches: (1) it simplifies implementing both OpenCL and CUDA host code by providing a simple-to-use, high-level abstraction API; (2) it supports executing arbitrary OpenCL and CUDA programs; (3) it allows conveniently targeting the devices of different nodes by automatically managing node-to-node communications; (4) it simplifies implementing data transfer optimizations by providing different, specially allocated memory regions, e.g., pinned main memory for overlapping data transfers with computations; (5) it optimizes memory management by automatically avoiding unnecessary data transfers; (6) it enables interoperability between OpenCL and CUDA host code for systems with devices from different vendors. Our experiments show that dOCAL significantly simplifies the development of host code for heterogeneous and distributed systems, with a low runtime overhead.

     

Hydrothermal synthesis of fluorescent silicon nanoparticles using maleic acid as surface-stabilizing ligands

Water-soluble silicon nanoparticles (SiNPs) have been synthesized with photoluminescence quantum yield more than 32% via a hydrothermal treatment of 3-aminopropyltriethoxysilane as silicon sources and maleic acid (MA) as surface-stabilizing ligands. Prepared SiNPs showed the presence of carboxylic acid groups through the incorporation of MA. The presence of 48.8 and 51.2% of Si–Si and Si–O binding was observed in the resulting carboxylic acid-functionalized SiNPs (COOH-SiNPs). As revealed by the fluorescence lifetime images, COOH-SiNPs possesses several fluorophores mainly composed of above Si–Si binding inside of single particle, which explains the excitation-dependent fluorescence emission behavior of COOH-SiNPs. Also, the presence of oxides mainly composed of Si–O binding and MA on the surface of COOH-SiNPs provides long-term stability for both fluorescence and dispersion. The potential use of COOH-SiNPs as fluorescence bioimaging agents for cellular media has been demonstrated. COOH-SiNPs showed excellent cell viability more than 91% for both MDAMB and MDCK cells even in 1,000 ppm concentration, and multicolor fluorescence imaging (blue, green, and red) of MDAMB cells was successfully accomplished with different excitation wavelengths.     

Non-isothermal calorimetric determination of precipitate interfacial energies

Equations suitable for computing specific interfacial energies of precipitates dissolving by a first order transformation were developed on the basis of the singularities taking place at the critical temperature,T _c, under equilibrium conditions. These equations employ data which can be determined by differential scanning calorimetry. Also the conditions for reaching dynamic equilibrium of particle volume fraction belowT _c are analysed in terms of a maximum permissible experimental heating rate. The results obtained for disperse order inCu-Al alloys are in good agreement with those expected from the observed particle features.     

Preparation of dextran cryogels for separation processes of binary dye and pesticide mixtures from aqueous solutions

We present mechanically strong macroporous, squeezable dextran cryogels as a column filling material for the removal and separation of binary organic dye and pesticide mixtures from aquatic medium. Dextran cryogels were prepared from aqueous solutions of dextran of various molecular weights (MWs) in the presence of 20 to 50 mol% divinyl sulfone (DVS) as a cross-linker at −18°C. The cryogels have interconnected irregular pores of 100 μm in sizes, and exhibit 69-84% reversible squeezability without damaging the 3D dextran network. Their total open pore volumes (6.3-10 mL g⁻¹), weight swelling ratios in water (1380%-2200%), and mechanical parameters could easily be adjusted by both DVS mol% and MW of dextran. Dextran cryogel with the highest modulus (3.8 ± 0.5 MPa), compressive stress (8 ± 2 MPa) and plateau stress (0.46 ± 0.04 MPa) was obtained at 50 mol% DVS using dextran with a MW of 15 to 25 kg·mol⁻¹. Dextran cryogels are hydrolysable at pH = 1 and 9 but stable at 7.4 independent on both the degree of cross-linking and MW of dextran. At below 50 mol% DVS, they are blood compatible and possess slight thrombogenic effect with blood clotting index value of 98% ± 5%. They are also capable to separate binary dye and pesticide mixtures from aqueous solutions via ionic interactions.     

Study of electrolyte effects on electrochemical synthesis and p-doping of poly(thienyl biphenyl) films

The electrochemical synthesis and charging–discharging process of a copolymer consisting of 3-octylthiophene (3-OT) and biphenyl units have been studied in different electrolytic media. The polymer material has been characterized by electrochemical and spectroscopic methods: cyclic voltammetry (CV), electrochemical quartz crystal microbalance (EQCM), chronopotentiometry, chronoamperometry and FTIR spectroscopy. The diffusion coefficients of different ions in poly(thienyl biphenyl) (PTB) films have been determined by chronoamperometry and compared with corresponding values in poly(3-octylthiophene) (POT) and poly(paraphenylene) (PPP). The best electrolytic conditions for synthesis of poly(thienyl biphenyl) concerning the copolymer structure was found to be in 0.1 M lithium hexafluoro arsenate (LiAsF₆) in acetonitrile. In this electrolyte solution, the content of phenylene segments compared to thienylene segments is highest resulting in a higher degree of cross-linking compared with films made in the presence of the other electrolyte salts studied.