Indentation deformation and cracking behavior of hydrated aluminoborate glasses

Aluminoborate glasses have recently been found to feature high resistance to crack initiation during indentation due to a highly flexible network structure. In cesium aluminoborate glasses, it has been found that the use of a simple post-treatment, namely aging in a humid atmosphere, can further improve this resistance. To better understand the mechanical properties of this glass family upon humid aging, we here study the effect of aging conditions on the structure and mechanical properties of Li,K,Cs-aluminoborate glasses. As expected, we find that higher humidity and longer aging time cause more pronounced permeation of atmospheric water into the glasses. Due to their denser structure and stronger modifier-oxygen bonds, the humid aging has a relatively smaller effect on the mechanical properties of Li- and K-containing glasses relative to Cs-containing glasses, with the latter achieving an ultrahigh crack resistance. We find that the humid aging leads to the formation of a hydration layer in the Cs-aluminoborate glass surface, with a thickness of around 26 μm upon aging at 23 °C with 40% relative humidity for 7 days. Moreover, a remarkable indentation behavior, that is, the observation of μm-sized shear bands inside the imprint of the Cs-glass upon aging at 60% relative humidity is reported. Taken as a whole, the work provides guidelines for how to control the humid aging rate as a function of relative humidity and temperature to form a hydration layer and thus achieve improved crack resistance in such glasses.     

Micro-Raman imaging of heterogeneous polymer systems: General applications and limitations

This article assesses the use of micro-Raman imaging with respect to polymer science. This relatively novel technique allows, at high spatial resolution, the acquisition of chemical and morphological information over an area of a sample. Using Raman imaging by confocal laser line scanning, a wide range of problems in polymer analysis has been studied to outline the capabilities and limitations of the technique. Three ternary polymer blends consisting of polypropene/polyethene/ethene-propene copolymer, polybutyleneterephthalate/polycarbonate/very low density polyethene, and styrene-co-acrylonitrile/styrene-co-maleicanhydrate/poly-2,6-dimethylphenylene oxide were studied with regard to compositional and morphological heterogeneities. In a binary polymer blend consisting of two different acrylate monomers, the refractive index profile established after artificially induced diffusion of the main components was determined from the concentration gradients. The distribution of unreacted free melamine in a cured melamine-formaldehyde resin was analyzed. Furthermore, the general structure of a composite sample consisting of polyethene fibers in an epoxide matrix was studied. Raman imaging proved suitable for the characterization of heterogeneities in composition and morphology on a size scale equal to or larger than 1 μm. In this sense, the technique helps to close the gap between infrared microscopy, with its comparatively poor spatial resolution, on the one hand, and transmission electron microscopy, with its limited chemical information, on the other hand. For heterogeneities on a submicron scale, the value of the technique is limited to the determination of average information. When combined with curve fitting, Raman imaging permitted us to determine the composition of the polypropene/polyethene/ethene-propene copolymer blend with an accuracy of 5–10%. The main limitations to micro-Raman imaging of polymer systems based on the confocal laser line scanning technique have been identified as the destruction of the samples due to insufficient heat dissipation of the high-incident laser power, interferences due to fluorescence, and the stability of the instrumentation during long collection times required for good signal-to-noise ratio spectra of weak Raman scatterers. © 1996 John Wiley & Sons, Inc.     

Modification of E-glass fiber surfaces with polyacrylic acid polymers from an aqueous solution

The research reported in the article focuses on modifying glass fiber surfaces with polyacrylic acid (PAA) compounds. E-glass fibers were treated with aqueous polyacrylic acid solution. Polyacrylic acid exchanges its protons with the ions present in the glass surface. Hydrolyzed metal cations may form salt complexes with the dissociated polyacrylic acid. Angular dependent electron spectroscopy for chemical analysis (ESCA) demonstrated that the atomic concentrations of aluminum and calcium in the glass fiber surface were constant throughout the analyzed interval. The cation exchange property of glass fiber was studied using direct current plasma (DCP), which showed that both calcium and aluminum ions were extracted by low concentration polycrylic acid solutions. ESCA studies of were extracted by low concentrationb polyacrylic acid solutions. ESCA studies of the PAA-treated glass fiber showed that the amount of PAA of the glass surface increases with increased acid concentration. A broadened and shifted ESCA peak of the carbon (0 CO) indicates the formation of salt complexes between the polyacrylic acid and metal ions on the glass surface. Polyacrylie acid was modified by an esterification reaction with glycidyl acrylate (GA) in aqueous solution in order to insert organofuctional groups into the PAA chain.     

Air entrapment in sheet molding compounds (SMC)

Entrapped air can commonly lead to large delaminations in thick walled sheet molding compound (SMC) products. In this work different sources of air entrapment in SMC are investigated. The critical process is shown to be the impregnation of the fibers. If no surface active additives are used, large volumes of air may be entrapped in this process, unless the viscosity of the compound is very low. In this situation of poor wetting, the viscosity of the compound during fiber impregnation will critically determine the interlaminar, tensile strength of the product. However, if surface active additives are used, the air escapes entrapment even at relatively high viscosities. The lowering of the viscosity, which is a side effect of the additives, has practically no importance under these conditions of good wetting. Large numbers of small air bubbles are also entrapped during the mixing of the components, but it is shown that these bubbles have very little effect on the mechanical properties of the finished part.     

Parabolic dish concentrators approximated by simple surfaces

Two different concentrating mirrors have been constructed that resemble parabolic dish reflectors. Both mirrors are made of slightly curved strips of flat, bendable material. The strips of the most simplified mirror have only large-radius circles and straight lines as boundaries. The necessary equations for making the mirrors are given. Also a simple way to make a stiff, lightweight frame and support for the mirror strips has been developed. Models of the mirrors have been built and successfully used for cooking and baking.     

In situ studies of the decomposition of ammonium uranyl carbonate in an electron microscope

An electron microscope has been used to study the reduction of ammonium uranyl carbonate (AUC) to UO₂. The reactions could be followed both in the diffraction and the lattice image mode. The first intermediate obtained was amorphous UO₃. Depending on the experimental conditions, either crystalline UO₂ was formed directly from this phase, or several other intermediates were indicated.Properties like crystallinity and crystallite size of final UO₂ were found to be a function of experimental conditions. Comparisons with properties of UO₂ from the industrial process have been made.     

Catalytic Encounters at the Molecular Level: Gabor A. Somorjai Award Symposium for Creative Research in Catalysis in Honor of Professor Manos Mavrikakis

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