Interparticle Potentials in Nonaqueous Silicon Nitride Suspensions

The rheological properties of nonaqueous silicon nitride suspensions are studied. Suspensions were prepared to volume fractions of solids of 0.21, 0.25, 0.29, and 0.33, and dispersed with phosphate ester in a mixture of solvents (methyl ethyl ketone, methyl isobutyl ketone, and cyclohexanone). Expanded viscosity curves were obtained by measuring under controlled rate and stress conditions, and the experimental data were fitted to the Cross model that provides the high shear limiting viscosity (η_∞). The evolution of viscosity with volume fraction of solids was fitted to the Krieger-Dougherty equation, to predict the maximum packing fraction (φ_m). The electrostatic pair potential was calculated based on the DLVO theory by evaluating the dielectric constant of the three-component solvent and the Hamaker constant of the Si₃N₄–solvent system. The surface potential was calculated by measuring the elastic modulus through dynamic rheological measurements. The steric potential was also evaluated from the available models. It has been observed that phosphate ester provides a purely steric stabilization at short separation distances (up to 9 nm), while electrostatic forces dominate at larger separation distances.     

Heavy Metals Bioremediation from Polluted Water by Glass-Ceramic Materials

The objective of this research was to study the removal of cadmium and lead from an aqueous solution through a biological treatment. For this purpose a glass-ceramic material was manufactured from industrial and urban wastes. Biofilms of microorganisms found in wastewater were developed on its surface, and continuous tests were conducted in the presence and absence of the biofilm to analyze the glass-ceramic's ability to remove the heavy metals from an aqueous environment. The results suggest that this bioremediation process, developed on an industrial scale, could represent an alternative to the chemical processes currently used.     

Modulation of Aβ42 Aggregation Kinetics and Pathway by Low-Molecular-Weight Inhibitors

The aggregation of amyloid-β 42 (Aβ42) is directly related to the pathogenesis of Alzheimer's disease. Here, we have investigated the early stages of the aggregation process, during which most of the cytotoxic species are formed. Aβ42 aggregation kinetics, characterized by the quantification of Aβ42 monomer consumption, were tracked by real-time solution NMR spectroscopy (RT-NMR) allowing the impact that low-molecular-weight (LMW) inhibitors and modulators exert on the aggregation process to be analysed. Distinct differences in the Aβ42 kinetic profiles were apparent and were further investigated kinetically and structurally by using thioflavin T (ThT) and transmission electron microscopy (TEM), respectively. LMW inhibitors were shown to have a differential impact on early-state aggregation. Insight provided here could direct future therapeutic design based on kinetic profiling of the process of fibril formation.     

Enhanced Hydrothermal Resistance of Y‐TZP Ceramics Through Colloidal Processing

Two commercial zirconia powders with 3 mol% of yttria (TZ3YE and TZ3YS, labeled as ZE and ZS, respectively) supplied by Tosoh (Japan) were used for this study. Maximum colloidal stability for ZE was achieved by dispersing the powders in a mixture of water/ethanol of 90:10 (wt/wt) using a sonication probe. The rheological behavior of the suspensions was optimized in terms of solids content ranging from 20 to 33 vol% and sonication time (0–6 min), the best results being obtained after 2 min. ZS samples were prepared to a solids loading of 30 vol% in water dispersing with 2 min‐sonication. Samples obtained by slip casting in plaster molds were used for dynamic sintering studies, and fully dense and nanostructured specimens were obtained at temperatures of 1300°C–1350°C (ZE samples) and 1400°C per 2 h (ZS samples). The Hardness (H) and Young's Modulus (E) properties of the specimens were studied by nanoindentation technique giving 17 and 250 GPa mean values for H and E, respectively. The specimens were then forced to a low‐temperature degradation (LTD) treatment at 130°C for 240 h in steps of 60 h. Raman spectroscopy and nanoindentation results of hydrothermally treated samples showed the absence of transformation from tetragonal to monoclinic phase until 180 h whereas the mechanical properties maintained constant even at the sample surface. After 240 h of LTD, the monoclinic phase was detected on all specimens by Raman peaks centered at 180, 191, and 383 cm^?1. The nanoindentation study revealed an important loss of mechanical features reaching 10 and 175 GPa for H and E, respectively. In the case of the ZS specimens, no monoclinic phase is detected after 240 h of LTD treatment and no decay of E or H is detected. The free defect microstructure reached for the ZS specimen revealed a higher hydrothermal resistance so that it is concluded that the excellent behavior against thermal degradation is possible due to the large uniformity obtained by colloidal processing rather than the particle size of the starting powders.     

Strength Analysis of Self-Supported Films Produced by Aqueous Electrophoretic Deposition

The goal of this work is to study the feasibility of the characterization of the fracture strength of porous alumina/zirconia thin layers by three-point bending and Weibull analysis. Films have been obtained by electrophoretic deposition on graphite and thermo-gelation of the deposit with carrageenan. On sintering, graphite is burned out and self-supported films are obtained. Strength values are well fitted to a simple two-parameter Weibull distribution. The fracture origins are subcritical growth cracks that originated at the surface irregularities associated with the processing method. A Weibull modulus around 3 is obtained.     

Electrochemical anticorrosion performance evaluation of Al2O3 coatings deposited by MOCVD on an industrial brass substrate

Alumina (Al₂O₃) coatings of different thickness were deposited on OT59 brass substrate (BS) using the metal organic chemical vapour deposition (MOCVD) technique to evaluate the corrosion performance by EIS measurements. The used precursor was dimethyl-aluminium-isopropoxide. Electrochemical characterizations of the deposited films were performed in a standard very aggressive acidic solution (aerated 1N H₂SO₄ at 25 °C up to 168 h of immersion time) by means of direct current method (Tafel curves) and electrochemical impedance spectroscopy (EIS). The Rutherford backscattering spectroscopy (RBS) indicated that the films are very pure with the correct Al₂O₃ stoichiometry, while the IR absorption spectra showed that the films did not contain any OH groups. The surface film morphology was investigated by atomic force microscopy (AFM) and displayed a globular texture. The films were very smooth, with a maximum root mean square roughness, for example, of 14 nm for a 0.96 μm thick coating. The EIS data confirmed, as expected, that a 2.40 μm Al₂O₃ layer ensures the best corrosion protection after 168 h of immersion in the very acidic environment used.     

Application of zeolitised coal fly ashes to the depuration of liquid wastes

In this study, the application of some zeolitised fly ashes and synthetic zeolites to the decontamination of the leachate produced in a municipal solid waste (MSW) treatment plant and to the liquid waste from a pig farm was analyzed. Thus, the reduction of organic matter (BOD and COD), ammonium and total nitrogen, phosphorus and metals contents after a zeolite treatment was evaluated. Several synthetic zeolites were tested: some commercial zeolites and other synthetic zeolites and zeolitised ashes obtained after a coal fly ash alkaline hydrothermal process. Two forms of contact between the zeolitic material and the liquid waste were tested: in a stirred tank and in a column. In addition, other variables determined were the amount of zeolite and the residence time. The results showed that zeolites, especially zeolitised fly ash, clearly produced a strong reduction in the leachate nitrogen and phosphorus content.     

Hydrodechlorination of 3-chloropyridine and chlorobenzene in methanol solution over alkali-modified zirconia-supported palladium catalysts

The liquid-phase hydrodechlorination of 3-chloropyridine and chlorobenzene has been studied over alkali-modified zirconia-supported palladium catalysts. The modification of the ZrO₂ with alkali metal carbonates improves the catalytic activity of the final palladium catalyst. Therefore, the larger the ionic radii (Li⁺ < Na⁺ < K⁺), the greater the catalytic activity (TOF) of the palladium catalyst. For 3-chloropyridine, hydrodechlorination proceeds without catalyst deactivation. This is explained as the result of the interaction of reaction products (pyridine and HCl) forming pyridinium chloride, thus avoiding the detrimental effect of HCl on the palladium particles. Catalytic hydrodechlorination of chlorobenzene over Pd catalysts exhibits an initial catalytic activity (TOF) much lower than that of 3-chloropyridine and the Pd catalysts deactivate as the reaction proceeds. Finally, chlorobenzene hydrodehalogenation has also been carried out in the presence of an equimolecular amount of pyridine resulting in a decrease in the initial reaction rate on the one hand, but also in an increase in final conversion on the other.     

Control of Polymer Composition in Pd‐Catalyzed CO/Olefin Terpolymerization Reactions

The CO/tert‐butylstyrene/ethylene terpolymerization catalyzed by Pd‐(N‐N′) complexes was studied. The results evidence that the olefin preferentially inserted in the terpolymer chain is strictly related to the nature of the nitrogen ligand, mainly to its steric constraints, and not to the kind of ligand. Indeed, slight variations in the backbone of the nitrogen ligands coordinated to palladium allow for the synthesis of terpolymers with a controlled composition.     

Binding of chlorpheniramine maleate to pharmacologically important alginic acid,carboxymethylcellulose, κ‐carageenan,and ι‐carrageenan as studied by diafiltration

The binding of cationic chlorpheniramine maleate (CPM) to the anionic water‐soluble polymers (WSPs) alginic acid, carboxymethylcellulose, κ‐carageenan, and ι‐carageenan was evaluated by diafiltration at pH 7.5 and in the absence and presence of 0.13M NaCl. CPM interacted with all of the WSPs when no NaCl was present in the solution, with charge‐related formation constants of around 700 M^?1 for all of the polymers, whereas the interactions were cleaved in the presence of 0.13M NaCl, indicating interactions of an electrostatic nature screened by the single electrolyte. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 598–602, 2005