The structure of microcrystalline cellulose (MCC) made by mild acid hydrolysis from cotton linter, flax fibres and sulphite or kraft cooked wood pulp was studied and compared with the structure of the starting materials. Crystallinities and the length and the width of the cellulose crystallites were determined by wide-angle X-ray scattering and the packing and the cross-sectional shape of the microfibrils were determined by smallangle X-ray scattering. The morphological differences were studied by scanning electron microscopy. A model for the changes in microfibrillar structure between native materials, pulp and MCC samples was proposed. The results indicated that from softwood or hardwood pulp, flax cellulose and cotton linter MCC with very similar nanostructures were obtained with small changes in reaction conditions. The crystallinity of MCC samples was 54-65%. The width and the length of the cellulose crystallites increased when MCC was made. For example, between cotton and cotton MCC the width increased from 7.1 nm to 8.8 nm and the length increased from 17.7 nm to 30.4 nm. However, the longest crystallites were found in native spruce wood (35-36 nm).

We report on the phase behavior of poly(9,9-dihexylfluorene) (PF6), poly(9,9-diheptylfluorene) (PF7), poly(9,9-dioctylfluorene) (PF8), poly(9,9-dinonylfluorene) (PF9), and poly(9,9-didecylfluorene) (PF10) in methylcyclohexane (MCH). After a heating-cooling cycle, in the 10-50 mg/mL concentration range, PF6/ MCH, PF7/MCH, PF8/MCH, and PF9/MCH systems were found to be gel-like, while PF10/MCH appears less viscous. PF6/MCH, PF7/MCH, PF8/MCH, and PF9/MCH form large (10-100 nm) sheetlike assemblies (thickness of 2-3 nm). The larger length scale structures of these sheets show an odd-even dependence on the side chain (spacer) length: the PF6 and PF8 sheets are broader and thinner, whereas PF7 and PF9 sheets are thicker with a putative double layer structure. PF10 does not follow this sequence, and only part of the polymer is assembled into a sheetlike structure, the rest remaining dissolved at the molecular level. PF8/MCH and PF9/MCH mixtures also have lower length scale crystalline structures with an internal period corresponding to the periodicity observed in the solid-state phase of PF8. Vestiges of crystalline domains are found for PF6 and PF7 but not for PF10. PF7/MCH, PF8/MCH, and PF9/MCH systems contain the conformational isomer C , of those chains observed in the phase, while this is not observed with other polymer/MCH systems.