Ordered mesoporous silica adsorbents were prepared by grafting amino- and carboxylic-containing functional groups onto MCM-41 for the removal of Acid blue 25 and Methylene blue dyes from wastewater. The amino-containing OMS−NH2 adsorbent has a large adsorption capacity and a strong affinity for the Acid blue 25. It can selectively remove Acid blue 25 from a mixture of dyes (i.e., Acid blue 25 and Methylene blue). The OMS−COOH is a good adsorbent for Methylene blue displaying excellent adsorption capacity and selectivity for the dye. The better selectivity of the OMS-based adsorbents means longer operating life and less maintenance. Furthermore, these adsorbents can be regenerated by simple washing with alkaline or acid solution to recover both the adsorbents and the adsorbed dyes.

Nanostructured TiO2 samples with primary particle size in the 4−20 nm range were prepared by either hydrothermal (H) or thermal (T) treatment of an amorphous precursor, and their behavior under UV illumination at 77 K was studied by means of EPR spectroscopy. The samples of the H series present the smallest crystallite size and after irradiation in a vacuum show some Ti3+ centers. In contrast, under these conditions only weak signals associated with oxygenated radicals are observed for the T samples. However, when oxygen is preadsorbed, several oxygenated complexes (O-, O2 -, O2H•, and O3 -) are photogenerated in proportions that depend on the characteristics of the material. Subsurface O- species are exclusively detected in the case of the samples of the H series, whereas ozonide radicals and surface O- are stabilized on materials with larger crystalline domains. These oxygenated complexes are thermally unstable, and they disappeared after warming to room temperature in the case of the T samples, but they are transformed to O2 - on the surface of the hydrothermally treated TiO2. Since adsorbed water and different types of free hydroxyls are present on these materials, as revealed by FTIR, a number of surface reactions have to be considered in order to account for the formation and stability of such photogenerated species.

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The dynamic growth processes of lamellae and spherulites of a polymer (BA-C8) synthesized by condensation polymerization of bisphenol A and 1,8-dibromooctane were directly observed using an atomic force microscope at 25 ( 1 °C. The phase shift measured at the tip of growing lamellae is lower than the phase shifts of the other regions of the lamellae. This result indicates that the growth front of a lamella is softer and contains more defects than the developed ones. The growth process of lamellae and the formation of spherulites were studied. A lamella was observed to breed more lamellae by inducing adjacent secondary nuclei and to develop into a lamellar sheaf and finally into a spherulite. The lamellae were preferentially oriented edge-on with respect to the surface of the BA-C8 polymer thin films. The detailed observations on the formation of the secondary nuclei indicated that the branching of the lamellae was only a temporary growth stage of the secondary lamellae. At the branch point, the secondary lamellae could propagate in both backward and forward directions with respect to the growth direction of the parent lamellae.

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