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Materials Science Forum Vol. 570
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Paper Title Page
Abstract: The effect of capping with Cu, Au and Pt of an array of Co nanoparticles is revised.
The magnetic surface anisotropy KS was found to be the dominant contribution to the
effective anisotropy Keff of the particles. Recent X-ray Magnetic Circular Dichroism
(XMCD) measurements show that there is hybridization between the 3d Co electrons
and the d and 4p electrons of the capping metal. By comparison to the mechanisms
which give rise to the surface anisotropy in thin films, it is argued that this hybridization
governs the modification of KS, and hence, of Keff.
1
Abstract: Nanocomposites of PA6 / organoclay at different concentration were prepared via melt
intercalation method using a corotating twin screw extruder. The composites were prepared with
Brazilian clay that was treated with different modifiers based on quaternary ammonium salts to
obtain three types of organoclays. After extrusion the mixtures were injection molded into
specimens that were tested to obtain the properties of tensile strength, notched izod impact and heat
deflection temperature. The structure and morphology of the nanocomposites were characterized by
x-rays diffraction (XRD) and transmission electron microscopy (TEM). The results showed that the
modifier “dodigen” which promoted the intermediate expansion of the bentonite clay within the
three salts used for the modification of the clay affects more significantly the mechanical properties,
HDT and morphology of the polyamide 6 due to the higher level of exfoliation observed in these
systems compared to the others modifiers. The improvement of the properties was correlated to the
level of exfoliation/intercalation obtained which depends on the process technique used, surface
treatment of the Brazilian clays with organic salts and interaction between polymer and clay.
18
Abstract: Copolymerization of silicon alkoxides in alcoholic basic medium using
trialkyl- or triarylchlorosilanes as terminator was investigated. Tetraethoxysilane
(TEOS), phenyltriethoxysilane (PTEOS) and vinyltriethoxysilane (VTEOS) were
used as monomers and triphenylchlorosilane (TPCS) and trimethylchlorosilane
(TMCS) as terminator. The copolymerization of TEOS with PTEOS and VTEOS
produces core-shell silica-silicone nanospherical hybrids containing large amounts of
functional groups in the structure of their external layer. The structure is the result of
the fast hopolymerization of TEOS in a first stage of the reaction, forming the core,
followed by copolymerization of TEOS and the alkyl- or vinyl-trialkoxysilane
comonomer in its last stage. The structure was confirmed by Raman and FTIR
spectroscopy, wide angle X-ray scattering (WAXS) and thermogravimetry. The
control of particle size is effectively made by the termination reaction and particles
with average diameter between 20 and 100 nm were obtained. Introduction of other
chemical functions on the surface of these nanoparticles can be carried out by
common reactions with the functional surface groups. As an example, sulfonation of
particles containing phenyl groups on the surface by direct sulfuric acid and
chlorosulfonic acid was investigated and the results discussed.
24
Abstract: In the development of metal hydrides for commercial applications, a special attention
should be devoted to the ways of production. For commercial success, the raw elements of the
hydrogen storage materials should be of low cost, the synthesis process should be inexpensive and
easily scalable. Therefore, it is important to put some effort on the elaboration of new and more
efficient means of producing metal hydrides. In this perspective, cold rolling was investigated as a
new means of producing nanocrystalline materials. This technique is well-known in the industry and
easily scalable. Cold rolling was performed on Mg-Ni system. The evolution of morphology, crystal
structure, crystallite size, deformation, and preferred orientation was studied as a function of
number of rolling passes. Cold rolling followed by a heat treatment produced the intermetallic
Mg2Ni. Without heat treatment and for a large number of rolling, an amorphous phase was
synthesized.
33
Abstract: A good method to store hydrogen is in it atomic form in crystalline structure of metals at
low pressure. Thanks to magnesium’s high hydrogen storage capacity, its low weight and its high
natural abundance, it is an attractive material to develop hydrogen solid state storage. The
production of Mg-based nanocomposites can enhance the kinetics of H-sorption of magnesium and
the temperature of release of hydrogen. Transition metals as iron, which have important catalytic
activity in hydrogen reactions with Mg, and the surface protective compound MgF2, are interesting
additions for magnesium mixtures for hydrogen storage. In this work, Mg-based nanocomposites
containing Fe and MgF2 were produced by reactive milling under hydrogen using the addition of
FeF3, or directly MgF2 and Fe. The efficiency of centrifugal and planetary mill in MgH2 synthesis
was compared. The phase evolution during different milling times (from 1 to 96 h) using the
planetary was investigated. The different H-desorption behavior of selected milled mixtures was
studied and associated with the different present phases in each case.
39
Abstract: AB2 metallic alloys provide large quantities of Laves phases when prepared using
conventional thermal routes. In the present work the crystallography, hydrogenation behavior and
mechanical milling (MM) effects of the pseudo-binary Zr(NbxV1-x)2 (0
45
Abstract: Structure, microstructure and hydriding properties of mechanically alloyed 2Mg-Ni
mixture were investigated. Two different nanocomposites were synthesized by mechanical alloying
(MA) in a low-energy planetary mill, namely MN100 (100 h of milling) and MN200 (200 h of
milling). The formation of nanocrystalline Mg2Ni was detected as a function of the milling time. An
appropriate combination of MA plus annealing under mild conditions accomplishes the complete
formation of Mg2Ni phase. The pressure-composition isotherms of the two samples reveal different
hydrogen storage capacities and plateau slopes. In addition, the low temperature Mg2NiH4
(LT)
formed by hydriding/cooling of MN100 h decomposes at 190 °C, whereas this hydride produced
from MN200 first transforms to the high temperature Mg2NiH4
and then decomposes near 245 °C.
The differences in the hydriding/dehydriding properties of MN100 and MN200 were associated
with the microstructure and structure of the phases formed during MA followed by heating under
argon/hydrogen.
52