In this paper we demonstrate that the sonication-driven exfoliation of aggregates and bundles of single-wall carbon nanotubes (SWNTs) in an aqueous surfactant solution can be easily monitored by UV-vis spectroscopy. The different stages of the exfoliation process were directly visualized by cryogenic temperature transmission electron microscopy, showing an excellent correspondence with the spectroscopic data: the maximum achievable exfoliation (which does not mean that 100% of the NTs are effectively exfoliated) corresponds to the maximum UV-vis absorbance of the NT solution. Moreover, it has been observed that NTs produced by the arc-discharge technology (Carbolex NTs) require less energy to achieve maximum exfoliation than NTs produced by chemical vapor deposition (HiPCO NTs). This difference is attributed to weaker van der Waals attraction between Carbolex NTs in the bundles and aggregates.

Silica‐coated vesicles have been produced by the deposition of silica onto unilamellar vesicles from aqueous solution for the first time. The quaternary ammonium surface of the surfactant vesicles is receptive to silica and facilitates deposition of up to 5–10 nm of it. The “petrified” vesicles are stable to dehydration and can be visualized by conventional TEM (see Figure) without additional staining agents.

The influence of organized media on polymerization reactions results in many cases in interesting morphologies of the polymeric material. In the present study, vesicle bilayers were used as ordered medium for the free radical polymerization of styrene. Cryo-electron microscopy gives evidence that the polymerization induces phase-separation phenomena leading to parachute-like morphologies. On the basis of general knowledge about vesicles and polymerizations in heterogeneous media, explanations for the observed phenomena are given. Bearing in mind that vesicles are outstanding models for membrane mimetic chemistry, it becomes evident that these findings can be relevant to the investigation of, for example, membrane-protein interactions.

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To determine the surface coverage of exfoliated carbon nanotubes by surfactant molecules, we propose four experimental methods based on thermogravimetric analysis, UV-vis spectroscopy, surface tension measurements, and a variant of Maron's titration. We apply all four methods to aqueous mixtures of carbon nanotubes and the surfactant sodium dodecyl sulfate and consistently find a surface coverage of between 1.5 and 2 g of surfactant per gram of carbon nanotubes. This corresponds to slightly more than two SDS molecules per square nanometer, which is comparable to the known maximum packing density of SDS at the air-water interface.

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The effect of catalyst partitioning over the organic and water phases in the catalytic chain transfer mediated miniemulsion polymerization was investigated and a mathematical model developed to describe the instantaneous degree of polymerization of the formed polymer. Experimental and predicted instantaneous degrees of polymerization prove to be in excellent agreement. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 5839–5849, 2008

Polystyrene−single-wall carbon nanotube (PS−SWNT) nanocomposites were prepared by directly mixing aqueous suspensions of exfoliated SWNTs and PS latex particles. After freeze-drying and compression molding, homogeneous polymer films were obtained with well-dispersed carbon nanotubes, as evidenced by scanning electron microscopy imaging. The nanocomposite films display a low percolation threshold and high levels of electrical conductivity. Simultaneously, a considerable increase in the glass-transition temperature of PS is achieved, provided that a sufficient amount of low-molar-mass PS is present in the matrix material. It is suggested that a certain extent of molar mass segregation occurs in the samples, with shorter PS chains preferentially adsorbed onto the nanotube surface. The latter wetting mechanism is indispensable for obtaining favorable electrical and thermal properties.