performance is related to the formation of a fine bulk heterojunction structure of polymer and PCBM domains as observed in AFM study.

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Physical chemical characterization of nanomaterials is critical to assessing quality control during production, evaluating the impact of material properties on human health and the environment, and developing regulatory frameworks for their use. We have investigated a set of 29 nanomaterials from four metal oxide families (aluminum, copper, titanium and zinc) with a focus on the measurands that are important for the basic characterization of dry nanomaterials and the determination of the dose metrics for nanotoxicology. These include crystalline phase and crystallite size, measured by powder X-ray diffraction, particle shape and size distributions from transmission electron microscopy, and specific surface area, measured by gas adsorption. The results are compared to the nominal data provided by the manufacturer, where available. While the crystalline phase data are generally reliable, data on minor components that may impact toxicity is often lacking. The crystal and particle size data highlight the issues in obtaining size measurements of materials with broad size distributions and significant levels of aggregation, and indicate that reliance on nominal values provided by the manufacturer is frequently inadequate for toxicological studies aimed at identifying differences between nanoforms. The data will be used for the development of models and strategies for grouping and read-across to support regulatory human health and environmental assessments of metal oxide nanomaterials.

A single-step processing method has been previously established to prepare porous alumina microstructures by a controlled sedimentation technique whereby fine powder from an aqueous suspension consolidates over a casting slab. Metastable surface chemical control of the suspension properties was able to produce a highly porous flat disc structure with a continuously increasing mean pore size from top to bottom. Formation of this gradient structure was facilitated by using a relatively broad particle size distribution. Top layer pore sizes less than 50 nm have been achieved. Without modification, these structures are suitable for use as ultrafiltration media.The present work presents a comparison of properties and performance data for samples made with the above mentioned functionally gradient characteristics, to samples made with a more uniform microstructure. The effects of sintering time and temperature were analysed in view of overall porosity, pore size distribution and the extent of densification from the green state. These results are presented along with permeation measurements from a filtration test module. Crown Copyright

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