Cellulose fibres, nanofibrils and microfibrils: The morphological sequence of MFC components from a plant physiology and fibre technology point of view
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During the last decade, major efforts have been made to develop adequate and commercially viable processes for disintegrating cellulose fibres into their structural components. Homogenisation of cellulose fibres has been one of the principal applied procedures. Homogenisation has produced materials which may be inhomogeneous, containing fibres, fibres fragments, fibrillar fines and nanofibrils. The material has been denominated microfibrillated cellulose (MFC). In addition, terms relating to the nano-scale have been given to the MFC material. Several modern and high-tech nano-applications have been envisaged for MFC. However, is MFC a nano-structure? It is concluded that MFC materials may be composed of (1) nanofibrils, (2) fibrillar fines, (3) fibre fragments and (4) fibres. This implies that MFC is not necessarily synonymous with nanofibrils, microfibrils or any other cellulose nano-structure. However, properly produced MFC materials contain nano-structures as a main component, i.e. nanofibrils.
KeywordsFibril Bacterial Cellulose Cellulose Fibre Plant Cell Wall Pulp Fibre
transmission electron microscopy
field emission scanning electron microscopy
atomic force microscopy.
Wood pulp fibres are presently a major area of research for several end-use applications. Fibres can be utilised as reinforcement in bio-degradable composites and as a source of raw materials for bio-energy and biochemical production. Wood pulp fibres have been applied as the raw material for the production of a fibrillated material, which was introduced and defined as microfibrillated cellulose (MFC) by Turbak et al.  and Herrick et al. . Several modern and high-tech nano-applications have been envisaged for MFC . Although cellulose fibres have constituted the main source for MFC production, the utilisation of other pulp fibres, agricultural crops and by-products have also been explored [3, 4, 5]. With the years, various subjective definitions have been given to the fibrillated materials, e.g. nanofibrillated cellulose, nanofibres, nanofibrils, microfibrils and nanocellulose [6, 7, 8, 9, 10].
The German philosopher Immanuel Kant (1724 to 1804) wrote: "Things which we see are not by themselves what we see... It remains completely unknown to us what the objects may be by themselves and apart from the receptivity of our senses. We know nothing but our manner of perceiving them...". Perception is thus a key word with respect to how we subjectively interpret structures. This is clearly exemplified in the relatively large number of terms that have been applied to roughly the same material, and emphasises the necessity of objectively clarifying and standardising the terminology applied within cellulose nanotechnology research. All the given terms relate to structures with nano-dimensions. However, is MFC a nano-structure? The purpose of this review is thus to shed more light on (1) the morphology of MFC structures, (2) the relationship between biological components of fibre wall structures and engineered cellulose-based nano-materials and (3) the terms associated with the MFC denomination. This review will not include other forms of cellulose materials, such as whiskers or bacterial cellulose, which may also be referred to as nanocellulose. For interested readers, see Klemm et al. .
The structure of wood pulp fibres
Chemical pulp fibres are produced through chemical pulping where lignin and hemicellulose are extracted. Chemical pulp fibres have a surface, which is characterised by a particular pattern created by wrinkles and microfibrils in the outer layers of the fibre wall structure (Figure 1a). The surface structure of chemical pulp fibres corresponds mainly to the primary and S1 layers of the fibre wall, which are preserved during chemical pulping. Contrary to the outer layers of the fibre wall (primary and S1 layers), the S2 layer is characterised by having a structure of microfibrils organised in a helical manner .
Elementary fibrils are generated in complex biological processes, involving cellulose synthase complexes in the plasma membrane, exocytosis of cell wall polymers and cortical microtubules . It seems to exist sufficient evidences that elementary fibrils in vascular plant cell walls are composed of 36 β-1,4-glucan chains, synthesised by the cellulose synthase proteins in the plasma membrane (rosette complexes) [22, 23].
Since the introduction of the transmission electron microscope, it seems that researchers have attempted to disintegrate cellulose fibres into single microfibrils/elementary fibrils for ultrastructural studies. Already in the 1950s, ultrasonic, hydrolysis and oxidation treatments were applied for disintegrating cellulose structures [14, 17, 24]. In addition, Ross Colvin and Sowden  reported a homogenization process based on beating for opening the structure of cellulose fibres and thus exposing the microfibril structures for transmission electron microscopy (TEM) analysis.
The disintegration of cellulose fibres into their structural components (microfibrils) has also found industrial interest. As mentioned above, in 1983, Turbak et al.  introduced a homogenisation procedure for fibrillating cellulose fibres with commercial purposes. The MFC terminology, which was originally applied to the fibrillated material, was probably related to the predominant structures encountered in fibre wall structures, i.e. microfibrils .
Components of microfibrillated cellulose
The fibril term has been applied for defining structures with a dimension less than 1 μm, although not consequently. Structures with diameters of <1.0 μm have also been observed in the fibre wall structure of pulp fibres. Such structures have been denominated macrofibrils, and diameters of approximately 0.66 μm have been reported . However, according to Meier , macrofibrils do not have definite dimensions. A fibril may also be considered an engineered structure as it is produced during mechanical fibrillation. There seems to be no concrete border line between fibrils and fibrillar fines (Figure 5A). Fibrillar fines may also be created through refining or beating, from mechanical and chemical pulp fibres, respectively . Subramanian et al.  considered fibrillar fines, microfines and microfibrillar cellulose in the same category, i.e. particles that pass a 75-μm diameter round hole or a 200-mesh screen of a fibre length classifier. Such a definition indicates that MFC may also be considered as fines, as exemplified in Figure 5A. Both materials are composed of relatively small and fibrillated components. However, according to Turbak et al. , no amount of conventional beating yields the microfibrillation obtained with an optimally homogenised product.
The microfibrillation mentioned by Turbak et al.  does not seem to refer to the creation of micrometre-sized particles but to the fibrillation of fibres into individualised microfibrils with diameters less than 100 nm . In this context, it is appropriate to introduce in this review a scale that has been widely emphasised during the last years within modern technology, i.e. "nano". It seems to be widely accepted that a nano-scale refers to sizes between 0.001 and 0.1 μm (1 to 100 nm). This implies that the nanofibril term refers to fibrils with diameters less than 100 nm. Based on this definition, it seems obvious that microfibrils can be considered nanofibrils, which also are composed of crystalline and amorphous regions. However, the difference between microfibrils and nanofibrils is that the former is a well-defined biological structure found in plant cell walls, whereas the latter can be considered a technological term introduced to describe secondary and engineered structures with diameters less than 100 nm.
As mentioned above, conventional MFC production yields materials with inhomogeneous sizes (Figures 3B,C, 4A and 5A). However, the fibrillation can be facilitated by, e.g. pre-treating the cellulose fibres enzymatically  or chemically [32, 33]. Pre-treatments have thus facilitated the production of homogeneous fibril qualities, with fibril diameters less than 100 nm (Figure 3E,F). In addition, some authors have reported a filtration procedure to remove poorly fibrillated fibres, thus maintaining mostly the fraction of homogeneous nanofibrils .
In general terms, the production of homogeneous fibril qualities may require major costs, including costs related to pre-treatments and to energy consumption during production. The less energy that is utilised, the less is the fibrillation of cellulose fibres and the less the amount of produced nanofibrils . Considering that conventional fibrillation (e.g. homogenisation without pre-treatment) produces a material that is inhomogeneous and may contain a major fraction of poorly fibrillated fibres and fines, can we state that MFC is a nano-structure? MFC per se is not necessarily a nano-material, but contains nano-structures, i.e. the nanofibrils (Figures 4 and 5). To define MFC as a nano-structure, it is necessary to give substantial evidence with respect to (1) the fraction of fibrillated fibres, (2) the fraction of nanofibrils and (3) the morphology of the nanofibrils in an MFC material. Provided that a given MFC is composed of an appropriate fraction of individualised nanofibrils, the MFC will have a major influence on the rheological, optical, mechanical and barrier properties of the corresponding materials.
Commonly, morphological evidences are given by microscopy and subjective evaluations. Researchers may focus on the visualisation of nano-structures, applying equipment designed for nano-assessment, e.g. FESEM, AFM and TEM. However, such equipment may limit the field of view considerably, which also introduces a subjective pre-selection of small areas containing nano-structures. Proper characterisation requires the quantification of the fibrillated material at several scales. This can include methods for assessing large areas, with a suitable resolution. One important aspect is not only the quantification of nanofibril morphology but also the quantification of fibres that are poorly fibrillated (see, e.g. Figure 3). Methods for assessing relatively large areas and structures at the micrometre scale are thus most valuable for complementing specialised devices for nano-characterisation.
It has been considered most important to propose an appropriate morphological sequence and definitions of MFC components. Microfibrils are important fibre wall components, i.e. biological nano-structures. However, due to the classical suffix "micro", microfibrils may be wrongly associated with micrometre-sized fibrils, which may be 1,000 times larger (>1 μm). According to evidences given in the literature and personal experience with characterisation of a variety of MFC qualities, it appears that MFC materials may be composed of (1) nanofibrils, (2) fibrillar fines, (3) fibre fragments and (4) fibres. This implies that MFC is not necessarily synonymous with microfibrils, nanofibrils or any other cellulose nano-structure. However, properly produced MFC materials contain nano-structures as a main component, i.e. nanofibrils.
All the images have been acquired by the author of this review, except Figure 2 which was acquired with the skilful cooperation of Yingda Yu (NTNU). Kristin Syverud (PFI) is acknowledged for valuable discussions and Philip André Reme (PFI) for revising the original manuscript.
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