Disposition of D-glucopyranosyl units on the surfaces of crystalline elementary fibrils of cotton cellulose

The results from two different chemical approaches to study the disposition of D -glucopyranosyl segments of the cellulose chains on the surfaces of microstructural units accessible to chemical reagents in cotton cellulose are compared, correlated, and rationalized. These studies provide the basis for a suggested disposition of D -glucopyranosyl units in the crystalline surfaces of elementary fibrils, for a proposed arrangement of hydrogen bonds on these surfaces, and for estimates of the size of the elementary fibrils.     

Characteristics and safety of nano-sized cellulose fibrils

A finely ground fibrillated cellulose was fractionated into separate size fractions. The characteristics of the smallest size fractions were studied, and the toxicity to humans was tested as part of a safety assessment. Morphological studies performed with state-of-the-art methods, such as scanning electron microscopy and atomic force microscopy, showed that the fraction obtained consisted of long thin fibrils but also larger fibril agglomerates, and spherical particles were present. The finest fraction did not show any sub-lethal effects as assessed by RNA inhibition test in vitro, nor were there any indications of genotoxicity as tested by the Ames test in vitro. Systemic effects tested in vivo with the nematode were also absent. No cytotoxic effects were seen in the highest tolerated dose test in vitro, but some indication of cytotoxicity was observed in the total protein content test in vitro at the highest sample concentration. The significance of this toxicity test result should be addressed in relation to the other toxicity tests, in which no toxicity was observed, with special emphasis on the in vivo test. Given this, the overall toxicity analyses support the conclusion that nano-scale cellulose fibrils can be considered to be safe towards humans. However, the reason for the positive cytotoxicity test result and, in addition, the effect of the biocide used in sample preservation on the toxicity tests need to be clarified before generalizing these results and declaring nanocellulose to be unambiguously safe.     

Visualization of cellulase interactions with cellulose microfibril by transmission electron microscopy

In this study, we developed a method to observe interactions between cellulase and cellulose microfibril by transmission electron microscopy. Although negative staining and low-angle metal shadowing increase image contrast, neither method is sufficient to view enzyme interactions with microfibril. However, we found that the combination of negative staining and low-angle metal shadowing provided better contrast for enzyme-like particles on the microfibril. The lengths of the particles interacting with microfibrils were 7.03 and 5.05 nm, parallel and perpendicular to the fiber direction, respectively. Accounting for the additional thickness owing to metal shadowing, the particle sizes were consistent with that of CBH I from Trichoderma reesei based on a crystalline structural analysis. The combination of these electron staining techniques successfully visualized morphological changes in microfibril as well as enzymes adsorbed on it, thus demonstrating cellulase in action. These results indicate that appropriate staining techniques can be applied to extend the applications of transmission electron microscopy, which may be particularly beneficial for studies on enzymatic behavior.     

Development of quality evaluation method for cellulose fibrils

Cellulose - Highly fibrillated cellulose, including cellulose micro or nanofibrils (CMFs or CNFs), has been extensively investigated. However, its morphological properties defined as the degree of...     

Magnetic alignment of the chiral nematic phase of a cellulose microfibril suspension

Stable suspensions of tunicate cellulose microfibrils were prepared by acid hydrolysis of the cellulosic mantles of tunicin. They formed a chiral nematic phase above a critical concentration. External magnetic fields were applied to the chiral nematic phase in two different manners to control its phase structure. (i) Static magnetic fields ranging 1-28 T were used to align the chiral nematic axis (helical axis) in the field direction. (ii) A rotating magnetic field (5 T, 10 rpm) was applied to unwind the helices and to form a nematic phase. These phenomena were interpreted in terms of the anisotropic diamagnetic susceptibility of the cellulose microfibril. The diamagnetic susceptibility of the microfibril is smaller in the direction parallel (chi( parallel)) to the fiber axis than in the direction perpendicular (chi( perpendicular)) to the fiber axis, that is, chi( parallel) < chi( perpendicular) < 0. Because the helical axis coincides with the direction normal ( perpendicular) to the fiber axis, the helical axis aligned parallel to the applied field. On the other hand, the rotating magnetic field induced the uniaxial alignment of the smallest susceptibility axis, that is, chi( parallel) in the present case, and brought about unwinding of the helices.     

Comparison of the characteristics of cellulose microfibril aggregates of wood, rice straw and potato tuber

The focus of this study has been to isolate cellulose microfibril aggregates by the one-time grinding treatment from wood, rice straw and potato tuber, and to compare their morphological and mechanical properties. Field emission scanning electron microscopy images showed that the diameter range of isolated microfibril aggregates from wood, 12–20 nm, was smaller than those from rice straw and potato tuber, 12–35 nm and 12–55 nm, respectively. These differences were observed even in the purified rice straws and potato tuber before the grinder treatment, but were hardly observed in the purified wood. The results of X-ray analysis and tensile tests indicated that there were no significant differences among the sources in the cellulose crystallinity and Young’s modulus of the isolated microfibril aggregates in the dry state. These results suggest that the inherent characteristics of cellulose microfibril aggregates in the dry state are very similar regardless of plant sources and tissue functions.     

Surface-templated formation of protein microfibril arrays.

Ordered arrays of collagen microfibrils form rapidly and spontaneously from a solution of monomers deposited onto a mica substrate. These arrays are well-ordered and apparently continuous over the entire substrate. Correlated atomic force microscope images and Laué diffraction patterns indicate that the protein alignment and microfibril formation is controlled by the crystal orientation of the mica substrate rather than fluid flow or drying effects. This surface-induced mechanism allows for immediate, robust, and reproducible pattern formation.     

Metal ion separations using cellulose phosphate as an ion-exchanger

Cellulose phosphate is used as a chelating ion-exchanger to effect the separation of several metal ions. Its exchange rate is much more rapid than that of a chelating ion-exchanger containing phosphonic acid groups on a polystyrene matrix. Weight distribution coefficients as a function of hydrogen ion concentration on cellulose phosphate are given for several metal ions. Successful separations of rare earths and alkaline earths, alkaline earths and alkali metals and aluminium and alkaline earths have been achieved on cellulose phosphate columns.     

Construction of a protein array on amyloid-like fibrils using co-assembly of designed peptides

Amyloid-like fibrils formed from de novo designed short peptides, made up a nanoscale scaffold on which streptavidin was arranged in a regular spacing, potentially allowing the development into an array technology utilizing bio-nanoconstructs.     

Size,shape, and arrangement of native cellulose fibrils in maize cell walls

Higher plant cell walls are the major source of the cellulose used in a variety of industries. Cellulose in plant forms nanoscale fibrils that are embedded in non-cellulosic matrix polymers in the cell walls. The morphological features of plant cellulose fibrils such as the size, shape, and arrangement, are still poorly understood due to its inhomogeneous nature and the limited resolution of the characterization techniques used. Here, we sketch out a proposed model of plant cellulose fibril and its arrangement that is based primarily on review of direct visualizations of different types of cell walls in maize using atomic force microscopy at sub-nanometer scale, and is also inspired by recent advances in understanding of cellulose biosynthesis and biodegradation. We propose that the principal unit of plant cellulose fibril is a 36-chain cellulose elementary fibril (CEF), which is hexagonally shaped and 3.2 × 5.3 nm in cross-section. Macrofibrils are ribbon-like bundles containing variable numbers of CEFs associated through their hydrophilic faces. As the cell expands and/or elongates, large macrofibril may split to become smaller bundles or individual CEFs, which are simultaneously coated with hemicelluloses to form microfibrils of variable sizes during biosynthesis. The microfibrils that contain one CEF are arranged nearly parallel, and the hydrophobic faces of the CEF are perpendicular to the cell wall surface. Structural disordering of the CEF may occur during plant development while cells expand, elongate, dehydrate, and die, as well as during the processing to prepare cellulose materials.     

The transparency and mechanical properties of cellulose acetate nanocomposites using cellulose nanowhiskers as fillers

Cellulose nanowhiskers (CNWs) were chemically modified by acetylating to obtain acetylated cellulose nanowhiskers (ACNWs) which could be well dispersed in acetone. The chemical modification was limited only on the surface of CNWs which was confirmed by transmission electron microscopy (TEM) and X-ray diffraction (XRD). Surface substitution degree of ACNWs was evaluated to be 0.45 through X-ray photoelectron spectroscopy (XPS). Fully bioresource-based nanocomposite films were manufactured by incorporation of ACNWs into cellulose acetate (CA) using a casting/evaporation technique. Scanning electron microscope (SEM) demonstrated that ACNWs dispersed well in the CA matrix, which resulted in high transparency of all CA nanocomposites. The tensile strength, Young’s modulus and strain at break of all CA nanocomposites exhibited simultaneous increase in comparison with neat CA matrix. At the content of 4.5 wt% ACNWs, the tensile strength, Young’s modulus and strain at break of the CA nanocomposite film were increased by 9, 39, and 44 % respectively.     

Harvesting fibrils from bacterial cellulose pellicles and subsequent formation of biodegradable poly-3-hydroxybutyrate nanocomposites

Bacterial cellulose has the potential to be used as a biodegradable, reinforcing component in composites due to its high strength and crystallinity. However it is often problematic to use in this context as it is difficult to separate its extensively bonded fibril network. This means it can be difficult for it to be incorporated as a fine dispersion into a composite and for the true benefits of the nanofibres to be realised in terms of physical property improvement in a conventional polymer format such as injection moulding. The method of sonication (using a range of experimental conditions) was utilised to harvest fibrils from the interwoven mesh of the cellulose pellicle, and then disperse them in different solvents to allow blending and subsequent casting. The novel step identified in this process was the sonication harvesting of the nanofibres undertaken on the highly hydrated as-received pellicle fresh from the reaction media (not the dried pellicle which could not be easily separated in the selected solvent). This unique step of harvesting directly from the fresh pellicle together with conventional sonication for dispersion in chloroform produced a bacterial cellulose/poly-3-hydroxybutyrate nanocomposite which showed excellent nanofibre dispersion and significant improvement in mechanical properties.     

The accessibility of cellulose as determined by dye adsorption

The accessibility of cotton cellulose was determined after it had been mercerized both in the slack and tension states. Mercerized samples were either dried or retained in the undried state before dyeing to determine their accessibilities by the adsorption of Direct Blue 1. Samples were characterized also by techniques such as moisture adsorption, water retention value (WRV) and X-ray analysis. It appeared that the crystallinity of cotton mercerized under tension was slightly increased during dyeing. Dye adsorption increased in the order nonmercerized <tension-mercerized <slack-mercerized. Products mercerized and not dried adsorbed more dye than counterparts given the same swelling treatment but dried after mercerization. The presence of dye in a sample mercerized and undried before dyeing did not affect its crystallinity. From both the dye adsorption and WRV data it was concluded that structural collapse of the fibre is greater for the slack-mercerized product than its tension-mercerized counterpart after it is dried. It was also concluded from dye adsorption and water adsorption data that about 34% of the internal surface of cotton and mercerized cotton, available for water adsorption, is inaccessible to Direct Blue 1.     

Structure and crystallization of sub-elementary fibrils of bacterial cellulose isolated by using a fluorescent brightening agent

The structure and crystallization of carefully isolated sub-elementary fibrils (SEFs) of bacterial cellulose have been investigated using TEM, WAXD, and high-resolution solid-state ¹³C NMR. The addition of a suitable amount of fluorescent brightener (FB) to the incubation medium of Acetobacter xylinum effectively suppressed the aggregation of the SEFs into the microfibrils, as previously reported. However, this study confirmed for the first time that serious structural change in the SEFs occurs during the removal of excess FB by washing with buffer solutions having pH values higher than 6 or with the alkaline aqueous solution that was frequently used in previous studies. In contrast, the isolation of unmodified SEFs was successfully performed by utilizing a washing protocol employing pH 7 citrate–phosphate buffer solution containing 1% sodium dodecyl sulfate. High-resolution solid-state ¹³C NMR and WAXD measurements revealed that the SEFs thus isolated are in the noncrystalline state in which the pyranose rings of the almost parallel cellulose chains appear to be stacked on each other. The respective CH₂OH groups of the SEFs adopt the gt conformation instead of the tg conformation found in cellulose I _α and I _β crystals, and undergo significantly enhanced molecular motion in the absence of intermolecular hydrogen bonding associated with these groups. The main chains are also subject to rapid motional fluctuations while maintaining the parallel orientation of the respective chains, indicating that the SEFs have a liquid crystal-like structure with high molecular mobility. Moreover, the SEFs crystallize into cellulose I _β when the FB molecules that may adhere to the surface of the SEFs are removed by extraction with boiling 70 v/v% ethanol and 0.1N NaOH aqueous solution. On the basis of these results, the crystallization of the SEFs into the I _α and I _β forms is discussed, including the possible formation of the crystalline-noncrystalline periodic structure in native cellulose.     

Readily hydrolysable cellulose esters as intermediates for the regioselective derivatization of cellulose; II. Soluble,highly substituted cellulose trifluoroacetates

Cellulose trifluoroacetate (CTFA) with DS values of 1.5 and 2.1 and DP values ranging from 170 to 800 have been prepared free from impurities of the reaction mixture (weakly bound trifluoroacetic acid) and of the procedure of isolation (diethyl ether). The CTFAs are soluble in DMSO, DMF, pyridine, and THF and thermostable up to 250 °C. A convenient synthetic method for CTFAs with DS 1.5 involves the acylation of cellulose with mixtures of trifluoroacetic acid (TFA) and trifluoroacetic anhydride (TFAA, 33% v/v) at room temperature for 4 h and subsequent treatment of the crude polymer at 150 °C and 80 Pa for 40 min. The preparation of CTFAs with DS-values up to 2.1 requires the addition of chloroform and 16 h reaction time.¹³ C-NMR studies as well as HPLC analyses after methylation and chain degradation show a preferred trifluoroacetylation of the primary hydroxy groups of the cellulose. The extent of depolymerization during the trifluoroacetylation was investigated for various cellulose materials. The cleavage of the trifluoroacetyl groups is possible by treating the derivative with a protic medium like water. Total hydrolysis of CTFA dissolved in DMF with water (room temperature) takes 6 min. The first paper on this topic was concerned with cellulose formates (Schnabelrauchet al., 1992).     

Atomic force microscopy and transmission electron microscopy of cellulose from Micrasterias denticulata; evidence for a chiral helical microfibril twist

Atomic force microscopy (AFM), tapping mode atomic force microscopy (TM-AFM) and transmission electron microscopy (TEM) have been used to image the cell wall, ultrathin sections of whole cells and cellulose microfibrils prepared from the green alga Micrasterias denticulata. Measurements of the microfibril dimensions are in agreement with earlier observations carried out by electron microscopy. Images at the molecular level of the surface of the microfibrils were obtained with AFM and show regular periodicities along the microfibril axis that correspond to the fibre and glucose repeat distances of cellulose. Twisted regions visible at intervals along the microfibrils dried down onto substrates were noted to be right-handed in over 100 observations by TEM, AFM and TM-AFM. This revised version was published online in August 2006 with corrections to the Cover Date.