Enhanced performance in the deteriorated area of multicrystalline silicon wafers by internal gettering

The deteriorated area of the multicrystalline silicon (mc‐Si) ingots grown by directional solidification, commonly known as the Red Zone, is usually removed before wafering. This area, characterized by poor minority carrier lifetime, is located on the sides, at the top, and the bottom of the mc‐Si ingots. In this study, the effect of internal gettering by oxygen precipitates and structural defects has been investigated on the bottom zone of a mc‐Si ingot. Nucleation and growth of oxygen precipitates as well as low temperature annealing were studied. Photoluminescence imaging, lifetime mapping, and interstitial iron measurements performed by μ‐PCD reveal a considerable reduction of the bottom Red Zone. An improvement of lifetime from below 1 µs to about 20 µs and a reduction of interstitial iron concentration from 1.32 × 10¹³ at/cm³ to 8.4 × 10¹⁰ at/cm³ are demonstrated in this paper. Copyright © 2013 John Wiley & Sons, Ltd.     

Nanopaper membranes from chitin–protein composite nanofibers—structure and mechanical properties

Chitin nanofibers may be of interest as a component for nanocomposites. Composite nanofibers are therefore isolated from crab shells in order to characterize structure and analyze property potential. The mechanical properties of the porous nanopaper structures are much superior to regenerated chitin membranes. The nanofiber filtration‐processing route is much more environmentally friendly than for regenerated chitin. Minerals and extractives are removed using HCl and ethanol, respectively, followed by mild NaOH treatment and mechanical homogenization to maintain chitin–protein structure in the nanofibers produced. Atomic force microscope (AFM) and scanning transmission electron microscope (STEM) reveal the structure of chitin–protein composite nanofibers. The presence of protein is confirmed by colorimetric method. Porous nanopaper membranes are prepared by simple filtration in such a way that different nanofiber volume fractions are obtained: 43%, 52%, 68%, and 78%. Moisture sorption isotherms, structural properties, and mechanical properties of membranes are measured and analyzed. The current material is environmentally friendly, the techniques employed for both individualization and membrane preparation are simple and green, and the results are of interest for development of nanomaterials and biocomposites. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2014 , 131, 40121.     

Air Flow and Compression Work in Vacuum Dewatering of Paper

Dewatering on the paper machine takes place by gravity, suction, pressing, and evaporation. Optimizing the operation of the vacuum system is important, since the electricity consumption of the vacuum pumps might be one-fifth of the total electricity consumption of the paper machine. Vacuum dewatering involves large volumes of air penetrating the web. The present study presents four sets of measured air flow rates useful for designing industrial equipment. The mass flux of air increases with increasing applied vacuum and decreases with increasing basis weight. Paper technological parameters, such as fiber size and fiber flexibility, also influence the mass flux.     

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.     

Competitive effects of free volume,rigidity, and self-adaptivity on indentation response of silicoaluminoborate glasses

Lithium aluminoborate glasses have recently been found to feature high resistance to crack initiation during indentation, but suffer from relatively low hardness and chemical durability. To further understand the mechanical properties of this glass family and their correlation with the network structure, we here study the effect of adding SiO₂ to a 25Li₂O–20Al₂O₃–55B₂O₃ glass on the structure and mechanical properties. Addition of silica increases the average network rigidity, but meanwhile its open tetrahedral structure decreases the atomic packing density. Consequently, we only observe a minor increase in hardness and glass transition temperature, and a decrease in Poisson's ratio. The addition of SiO₂, and thus removal of Al₂O₃ and/or B₂O₃, also makes the network less structurally adaptive to applied stress, since Al and B easily increase their coordination number under pressure, while this is not the case for Si under modest pressures. As such, although the silica-containing networks have more free volume, they cannot densify more during indentation, which in turn leads to an overall decrease in crack resistance upon SiO₂ addition. Our work shows that, although pure silica glass has very high glass transition temperature and relatively high hardness, its addition in oxide glasses does not necessarily lead to significant increase in these properties due to the complex structural interactions in mixed network former glasses and the competitive effects of free volume and network rigidity.     

Synthesis and Reactivity of Iron(II) Complexes with a New Tripodal Imine Ligand

A new tripodal imine ligand tris(2-(propan-2-ylideneamino)ethyl)amine (imine₃tren) was prepared in order to stabilize high valent iron-oxido complexes. Iron complexes were synthesized in template reactions from iron(II) salts, tris(2-aminoethyl)amine (tren) and acetone. Due to the reversibility of the imine formation, complexes with different ligands were obtained depending on the reaction conditions. Three complexes, [Fe(imine₃tren)(OAc)₂] ( 1 ), [Fe(imine₃tren)(OAc)]OTf ( 2 ) and [(imine₃tren)₂Fe₂(F)₂](SbF₆)₂ ( 3 ), could be synthesized and structurally characterized. However, reactions with hydrogen peroxide, iodosobenzene or ozone did not lead to any kind of “oxygen adduct” complex that could be spectroscopically observed.     

Antioxidant capacity and total phenolics of <Emphasis Type="Italic">Cyphostemma digitatum</Emphasis> before and after processing: use of different assays

In the framework of standardisation of new healthy food sources, this paper aimed to study the total phenolics and the antioxidant power of Cyphostemma digitatum (Vitaceae) in water and ethanol extracts, using 96-well micro plates with BMG FLUOstar Optima micro plate reader. Total phenolics by Folin–Ciocalteu method in the water extracts were significantly lower after processing, decreasing from 1.41 ± 0.06 g GAE/100 g in the raw leaves to 0.80 ± 0.08 g GAE/100 g in the processed sample; the ethanol extract revealed the same trend with higher values, decreasing from 1.95 ± 0.03 to 1.56 ± 0.12 g GAE/100 g. The antioxidant capacity was elucidated by four methods: TEAC, DPPH, FRAP and ORAC. No or very weak correlations were found between antioxidant assays and total phenolics; this confirms that the antioxidant capacity could be attributed to other molecules. The ORAC assay proved to be more powerful than the other assays; it showed 103.3 ± 2.5 mmol/100 g Trolox equivalents in the raw leaves ethanol extract and 91.9 ± 3.0 mmol/100 g in the processed sample. ORAC assay showed the opposite for the water extract where the antioxidant capacity increased from 16.7 ± 0.2 to 41.7 ± 2.7 mmol/100 g Trolox equivalents after processing, which could be attributed to new water-soluble compounds generated in the consumed form.     

MgAl2O4-Spinel Synthesized by High-Energy Ball Milling and Reaction Sintering

A new way to prepare magnesia-alumina-spinel was investigated making use of a mixed powder system of MgO and metallic Al-3 wt% Mg. Intensive ball milling was applied which provides the formation of new powder particles as composite of both components in intimate contact. The new configuration of the particles had a significant impact on the reaction sintering behavior leading to single phase spinel microstructures at moderate temperatures below 1400°C. Optimized milling of the powder mixture was therefore required providing reduced crystallite sizes and strongly enlarged interfacial area shared by the reacting components. The optimal milling time was identified by the complete reaction of the starting powders to spinel during sintering. Shorter milling times led to incomplete reactions and longer milling times contaminated the milling product by debris from the milling tools. The amount of interfaces generated by the intimate mixing dominated the sintering reaction kinetics whereas the specific surfaces area was of secondary importance.