The ability of macrocyclic ligands to facilitate formation of dispersions of single-walled carbon nanotubes (SWNTs) was investigated using a combination of absorption spectrophotometry and optical microscopy. Vacuum filtration of aqueous dispersions containing SWNTs and various macrocyclic ligands (derivatised porphyrin, phthalocyanine, cyclodextrin and calixarene) afforded self-supporting membranes known as buckypapers. Microanalytical data and energy dispersive X-ray spectra were obtained for these buckypapers and provided evidence for retention of the macrocyclic ligands within the structure of the membranes. The electrical conductivities of the membranes varied between 30 ± 20 and 220 ± 60 S cm−1, while contact angle analysis revealed they all possessed hydrophilic surfaces. The mechanical properties of buckypapers prepared using macrocyclic ligands as dispersants were shown to be comparable to that of a benchmark material prepared using the surfactant Triton X-100 (Trix). Incorporation of the macrocyclic ligands into SWNT buckypapers was found to increase their permeability up to ten-fold compared to buckypapers prepared using Trix. No correlation was observed between the water permeability of the membranes and the average size of either their surface or internal pores. However, the water permeability of the membranes was found to be inversely dependent on their surface area. The ability of macrocyclic ligands to facilitate formation of dispersions of single-walled carbon nanotubes (SWNTs) was investigated using a combination of absorption spectrophotometry and optical microscopy. Vacuum filtration of aqueous dispersions containing SWNTs and various macrocyclic ligands (derivatised porphyrin, phthalocyanine, cyclodextrin and calixarene) afforded selfsupporting membranes known as buckypapers. Microanalytical data and energy dispersive X-ray spectra were obtained for these buckypapers and provided evidence for retention of the macrocyclic ligands within the structure of the membranes. The electrical conductivities of the membranes varied between 30 AE 20 and 220 AE 60 S cm À1

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To investigate excess-hydrolysis of titanium alkoxides, TiO 2 powders were fabricated from titaniumtetra-isopropoxide using 6:1 and 100:1 H 2 O:Ti (r) ratios. Powders were dried and fired at a range of temperatures (≤800ºC). Hydroxylation and organic content in powders were characterised using ATR-FTIR, laser Raman microspectroscopy, and elemental microanalysis; surface area and pore size distribution were evaluated using N 2 gas adsorption; phase composition was analysed using XRD and laser Raman microspectroscopy; and crystallite size was evaluated by XRD, TEM and SEM. Results showed near-complete hydrolysis in a predominantly aqueous medium (r = 100), resulting in precipitated crystalline powders exhibiting brookite and anatase, which begin to transform to rutile below 500°C. Powders precipitated in a predominantly organic medium (r = 6) underwent partial hydrolysis, were highly porous and exhibited an amorphous structure, with crystallisation of anatase occurring at ~300°C and transformation to rutile beginning at 500°-600°C. D.A.H. Hanaor et al

Rutile powder was synthesized via sol–gel processing of Tyzor TE precursor in an aqueous solution at 40°C–50°C. A suite of characterization techniques, including FTIR, Raman, X‐ray, and electron diffraction, were employed to investigate the microstructural evolution. The synthesized powder was phase‐pure rutile possessing high surface area (144.7 m2/g), an average pore size of 24.9 nm, and pore volume of 0.66 cm3/g. A reaction mechanism is proposed for the preferential evolution of rutile over other titania polymorphs (i.e. amorphous or anatase).

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