The crystal and molecular structure together with the hydrogen-bonding system in cellulose Ibeta has been determined using synchrotron and neutron diffraction data recorded from oriented fibrous samples prepared by aligning cellulose microcrystals from tunicin. These samples diffracted both synchrotron X-rays and neutrons to better than 1A resolution (>300 unique reflections; P2(1)). The X-ray data were used to determine the C and O atom positions. The resulting structure consisted of two parallel chains having slightly different conformations and organized in sheets packed in a "parallel-up" fashion, with all hydroxymethyl groups adopting the tg conformation. The positions of hydrogen atoms involved in hydrogen-bonding were determined from a Fourier-difference analysis using neutron diffraction data collected from hydrogenated and deuterated samples. The hydrogen atoms involved in the intramolecular O3...O5 hydrogen bonds have well-defined positions, whereas those corresponding to O2 and O6 covered a wider volume, indicative of multiple geometry with partial occupation. The observation of this disorder substantiates a recent infrared analysis and indicates that, despite their high crystallinity, crystals of cellulose Ibeta have an inherent disorganization of the intermolecular H-bond network that maintains the cellulose chains in sheets.

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The crystal and molecular structure, together with the hydrogen-bonding system in cellulose I(alpha), has been determined using atomic-resolution synchrotron and neutron diffraction data recorded from oriented fibrous samples prepared by aligning cellulose microcrystals from the cell wall of the freshwater alga Glaucocystis nostochinearum. The X-ray data were used to determine the C and O atom positions. The resulting structure is a one-chain triclinic unit cell with all glucosyl linkages and hydroxymethyl groups (tg) identical. However, adjacent sugar rings alternate in conformation giving the chain a cellobiosyl repeat. The chains organize in sheets packed in a "parallel-up" fashion. The positions of hydrogen atoms involved in hydrogen-bonding were determined from a Fourier-difference analysis using neutron diffraction data collected from hydrogenated and deuterated samples. The differences between the structure and hydrogen-bonding reported here for cellulose I(alpha) and previously for cellulose I(beta) provide potential explanations for the solid-state conversion of I(alpha) --> I(beta) and for the occurrence of two crystal phases in naturally occurring cellulose.

Cellulose from the cell wall of the green alga Microdictyon tenuius was studied by electron diffraction. The diffractograms disclose two distinct crystalline phases. The major phase has a one-chain, triclinic (PI) structure with unit cell parameters of a = 0.674 nm, b = 0.593 nm, c (chain axis) = 1.036 nm, a = 117°, 0 = 113°, and y = 81°. The crystal unit cell of the minor component has two chains and is monoclinic (P2i), with a -0.801 nm, b = 0.817 nm, c (chain axis) = 1.036 nm, and y the monoclinic angle = 97.3°. The triclinic phase is metastable, and annealing it in dilute alkali at 260 °C converts it into the monoclinic form. The presence of two phases in Microdictyon can be extended to other algal celluloses and is consistent with the biphasic character deduced from 13C CP/MAS NMR spectroscopy. The triclinic and the monoclinic structures correspond to the la and Id spectra, respectively.

Composite materials were processed by casting a mixture of aqueous suspensions of latex and microfibrils. These microfibrils, or whiskers, are extracted from a sea animal and are monocrystals of cellulose, with an aspect ratio around 100 and an average diameter of 20 nm. It has been found that the mechanical properties (shear modulus) are increased by more than two orders of magnitude in the rubbery state of the polymeric matrix, when the whisker content was 6% (w/w). This very large effect is discussed on the basis of different types of mechanical models and it is concluded that these whiskers form a rigid network, probably linked by hydrogen bonds. The formation of this network is assumed to be governed by a percolation mechanism.

A revised crystal structure for mercerized cellulose based on high-resolution synchrotron X-ray data collected from ramie fibers is reported (space group P2(1), a = 8.10(3) A, b = 9.03(3) A, c = 10.31(5) A, gamma = 117.10(5) degrees; 751 reflections in 304 composite spots; theta < 21.11 degrees; lambda = 0.7208 A; LALS refinement with d > 1.5 A, R' ' = 0.16; SHELX97 refinement with d > 1 A, R = 0.21). As with regenerated cellulose the crystal structure consists of antiparallel chains with different conformations but with the hydroxymethyl groups of both chains near the gt position. However, the conformation of the hydroxymethyl group of the center chain in the structure reported here differs significantly from the conformation in regenerated cellulose. This may be related to a large observed difference in the amount of hydroxymethyl group disorder: approximately 30% for regenerated cellulose and approximately 10% for mercerized cellulose.

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Cellulose whiskers resulting from HCl acid hydrolysis of tunicin were subjected to TEMPO-mediated oxidation under various conditions and the extent of the resulting oxidation was characterized by Fouriertransform infrared spectroscopy (FT-IR), conductimetry, X-Ray diffraction analysis and transmission electron microscopy (TEM). With degree of oxidation of up to 0.1 the samples kept their initial morphological integrity and native crystallinity, but at their surface the hydroxymethyl groups were selectively converted to carboxylic groups, thus imparting a negative surface charge to the whiskers. When dispersed in water these oxidized whiskers did not flocculate and their suspensions appeared birefringent when viewed between cross polarizers, thus indicating a liquid crystalline behavior.