Rheology and structure formation in diluted mixed particle-surfactant systems.

In the present work, we focus on the bulk rheology of mixtures consisting of surfactant modified silica nanoparticles in water. Depending on the ratio of surfactant and nanoparticle concentrations, significant modifications in the measured rheology are evidenced. A domain where the dispersions behave like viscoelastic media is observed. Outside this domain, the dispersions exhibit viscous properties. The changes in the bulk rheology characteristics are discussed in terms of interaction effects between the surfactant and the particles. The results obtained are seen in the context of diluted emulsions' properties and characteristics.

Synthesis of imogolite fibers from decimolar concentration at low temperature and ambient pressure: a promising route for inexpensive nanotubes.

To date, the successful low-temperature synthesis of the aluminosilicate imogolite nanotubes always involved initial concentrations of the reagents in the millimolar range, higher concentrations being reported to lead to the formation of the less well characterized allophane phase. The present work shows that reaction kinetics and not initial concentration control the formation of the nanotubes: substantial amounts of well formed imogolite were obtained from a decimolar initial concentration, i.e. 100 times higher than the "standard" protocol. The allophane-like spheroids expected from the high reagent concentration were not observed in this work, and proto-imogolite was obtained instead.

Synthesis of large quantities of single-walled aluminogermanate nanotube.

A simple aqueous synthesis yielded about 100 times more structurally well-organized single-walled aluminogermanate nanotubes than previously reported "standard" procedures. The structure analyses using XRD, IRTF, TEM, and XAS were greatly facilitated by the high concentrations available, and they ascertained the imogolite-like structure of the nanotubes. Simplicity and yield of the synthesis protocol are likely to favor commercial applications of theses materials as well as simplified syntheses of other nanophases.

Role of molting on the biodistribution of CeO2 nanoparticles within Daphnia pulex.

As all arthropods, microcrustaceans shed their chitinous exoskeleton (cuticule, peritrophic membrane) to develop and grow. While the molting is the most crucial stage in their life cycle, it remains poorly investigated in term of pollutant biodistribution within the organisms. In this paper, we used optical, electronic, and X ray-based microscopies to study the uptake and release of CeO2 nanoparticles by/from Daphnia pulex over a molting stage. We measured that D. pulex molts every 59 ± 21 h (confidence interval) with growth rates about 1.1 or 1.8 µm per stage as a function of the pieces measured. Ingestion via food chain was the main route of CeO2 nanoparticles uptake by D. pulex. The presence of algae during the exposure to nanoparticles (sub-lethal doses) enhanced by a factor of 3 the dry weight concentration of Ce on the whole D. pulex. Nanoparticles were localized in the gut content, in direct contact with the peritrophic membrane, and on the cuticle. Interestingly, the depuration (24 h with Chlorella pseudomonas) was not efficient to remove the nanoparticles from the organisms. From 40% to 100% (depending on the feeding regime during exposure) of the CeO2 taken up by D. pulex is not release after the depuration process. However, we demonstrated for the first time that the shedding of the chitinous exoskeleton was the crucial mechanism governing the released of CeO2 nanoparticles regardless of the feeding regime during exposure.

Nanobacteria-like calcite single crystals at the surface of the Tataouine meteorite.

Nanobacteria-like objects evidenced at the surface of the orthopyroxenes of the Tataouine meteorite in South Tunisia have been studied by scanning and transmission electron microscopies. A method of micromanipulation has been developed to ensure that exactly the same objects were studied by both methods. We have shown that the nanobacteria-like objects are spatially correlated with filaments of microorganisms that colonized the surface of the meteoritic pyroxene during its 70 years of residence in the aridic Tataouine soil. Depressions of a few micrometers in depth are observed in the pyroxene below the carbonates, indicating preferential dissolution of the pyroxene and calcite precipitation at these locations. The nanobacteria-like small rods that constitute calcium carbonate rosettes are well crystallized calcite single crystals surrounded by a thin amorphous layer of carbonate composition that smoothes the crystal edges and induces rounded shapes. Those morphologies are unusual for calcite single crystals observed in natural samples. A survey of recent literature suggests that the intervention of organic compounds derived from biological activity is likely in their formation.

Piezoelectric tantalum pentoxide studied for optical tunable applications.

Piezoelectric transparent thin films are of great interest for use in tunable filters. We present experimental results on Ta2O5 single layers coated on fused-silica substrates with an electron-beam deposition process. Above 450 degrees C, coatings change from an amorphous to a polycrystallized structure. When this structure shows a preferred orientation matching the piezoelectric tensor of the Ta2O5 crystal and the external electric field, variation in the piezoelectric layer thickness is expected. We detail experimental results in terms of optical (spectrophotometric and scattering measurements) and nonoptical characterizations (x-ray diffraction and scanning electron microscopy). Then the resultant thickness variation under oscillating applied voltage is measured with an extrinsic Fabry-Perot interferometer setup.