High-performance Materials (high-performance + material)

Distribution by Scientific Domains


Selected Abstracts


Epitaxial Growth of Indium Arsenide Nanowires on Silicon Using Nucleation Templates Formed by Self-Assembled Organic Coatings,

ADVANCED MATERIALS, Issue 14 2007
T. Mĺrtensson
Indium arsenide nanowires are grown directly on silicon substrates (see figure and cover) using a method employing self-assembled organic coatings to create oxide-based growth templates. High-performance materials, such as InAs, could have great impact on future nanoelectronics if integrated with Si, but integration has so far been hard to realize with other methods. [source]


Degradation of aramid fibers under alkaline and neutral conditions: Relations between the chemical characteristics and mechanical properties

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010
G. Derombise
Abstract Aramid fibers are high-performance materials that have been used in various applications such as heat and cut protection, composites, rubber reinforcement, ropes and cables, and fabrics; today their use is proposed in geotextiles for alkaline ground reinforcement, and they have been used in cables for marine applications for a few years. However, there is a lack of experience with the long-term behavior of aramid fibers in wet and alkaline environments. Aging studies were therefore performed on Twaron 1000 fibers under different conditions (sea water, deionized water, pH 9, and pH 11). Hydrolytic degradation was evaluated with Fourier transform infrared and viscosimetry measurements, which were correlated with tensile test measurements. The tensile strength followed a logarithmic evolution with the aging time, whereas the modulus remained constant. A linear relation between the tensile strength and the reduced viscosity of the hydrolytically aged fibers is highlighted. Aging indicators are proposed that allow the hydrolytic degradation to be quantified. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]


Recycled PET nanocomposites improved by silanization of organoclays

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 2 2007
Milan Krá, alík
Abstract Recycled PET/organo-modified montmorillonite nanocomposites were prepared via melt compounding as a promising possibility of the used beverage bottles recovery. According to our previous work, the three suitable commercial organoclays Cloisite 25A, 10A, and 30B were additionally modified with [3-(glycidyloxy)propyl]trimethoxysilane, hexadecyltrimethoxysilane and (3-aminopropyl)trimethoxysilane. The selected organoclays were compounded in the concentration 5 wt % and their degree of intercalation/delamination was determined by wide-angle X-ray scattering and transmission electron microscopy. Modification of Cloisite 25A with [3-(glycidyloxy)propyl]trimethoxysilane increased homogeneity of silicate layers in recycled PET. Additional modification of Cloisite 10A and Cloisite 30B led to lower level of delamination concomitant with melt viscosity reduction. However, flow characteristics of all studied organoclay nanocomposites showed solid-like behavior at low frequencies. Silanization of commercial organoclays had remarkable impact on crystallinity and melt temperature decrease accompanied by faster formation of crystalline nuclei during injection molding. Thermogravimetric analysis showed enhancement of thermal stability of modified organoclays. The tensile tests confirmed significant increase of PET-R stiffness with organoclays loading and the system containing Cloisite 25A treated with [3-(glycidyloxy)propyl]trimethoxysilane revealed combination of high stiffness and extensibility, which could be utilized for production of high-performance materials by spinning, extrusion, and blow molding technologies. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 [source]


Synthesis and Properties of Novel Fluorinated Poly(phenylene- co -imide)s

MACROMOLECULAR CHEMISTRY AND PHYSICS, Issue 3 2007
Wenmu Li
Abstract A new class of high-performance materials, fluorinated poly(phenylene- co -imide)s, were prepared by Ni(0)-catalytic coupling of 2,5-dichlorobenzophenone with fluorinated dichlorophthalimide. The synthesized copolymers have high molecular weights (,=,5.74,×,104,17.3,×,104 g,·,mol,1), and a combination of desirable properties such as high solubility in common organic solvent, film-forming ability, and excellent mechanical properties. The glass transition temperature (Tgs) of the copolymers was readily tuned to be between 219 and 354,°C via systematic variation of the ratio of the two comonomers. The tough polymer films, obtained by casting from solution, had tensile strength, elongation at break, and tensile modulus values in the range of 66.7,266 MPa, 2.7,13.5%, and 3.13,4.09 GPa, respectively. The oxygen permeability coefficients () and permeability selectivity of oxygen to nitrogen () of these copolymer membranes were in the range of 0.78,3.01 barrer [1 barrer,=,10,10 cm3 (STP) cm/(cm2,·,s,·,cmHg)] and 5.09,6.25, respectively. Consequently, these materials have shown promise as engineering plastics and gas-separation membrane materials. [source]