|Home | About | Journals | Submit | Contact Us | Français|
Liquid crystalline cellulosic-based solutions described by distinctive properties are at the origin of different kinds of multifunctional materials with unique characteristics. These solutions can form chiral nematic phases at rest, with tuneable photonic behavior, and exhibit a complex behavior associated with the onset of a network of director field defects under shear. Techniques, such as Nuclear Magnetic Resonance (NMR), Rheology coupled with NMR (Rheo-NMR), rheology, optical methods, Magnetic Resonance Imaging (MRI), Wide Angle X-rays Scattering (WAXS), were extensively used to enlighten the liquid crystalline characteristics of these cellulosic solutions. Cellulosic films produced by shear casting and fibers by electrospinning, from these liquid crystalline solutions, have regained wider attention due to recognition of their innovative properties associated to their biocompatibility. Electrospun membranes composed by helical and spiral shape fibers allow the achievement of large surface areas, leading to the improvement of the performance of this kind of systems. The moisture response, light modulated, wettability and the capability of orienting protein and cellulose crystals, opened a wide range of new applications to the shear casted films. Characterization by NMR, X-rays, tensile tests, AFM, and optical methods allowed detailed characterization of those soft cellulosic materials. In this work, special attention will be given to recent developments, including, among others, a moisture driven cellulosic motor and electro-optical devices.
Cellulose, the main constituent of plant cell walls, is a linear polysaccharide (Figure 1), which is mainly used to produce paper. However, in this work we are more interested in soft materials obtained from converted cellulose, not only into nano rods, but also in cellulose derivatives. In 1976, Gray reported that concentrated solutions of cellulose derivatives could self-assemble into ordered phases . Those liquid crystalline phases displayed colors that changed with concentration and viewing angle, which were attributed to a cholesteric structure. The maximum peak wavelength (λ0) reflected by the samples for incident light normal to the surface may be expressed as, λ0 = nePcosθ, where ne is the average refractive index; P the helical pitch; and θ the angle between the light propagation direction and the helix axis . The values of λ0 may, therefore, be tuned by altering the helical pitch or the average refractive index of the chiral nematic material. Some theories were proposed to interpret the variation of the pitch with polymer concentration. For example, the theory proposed by Kimura et al.  predicts a linear dependence of the reciprocal pitch against ϕ(1 – ϕ/3)/(1 – ϕ)2, where ϕ is the polymer concentration, which is in fairly good agreement with the experiments . Due to cellulose relatively stiff cellulose backbone, which forces a parallel orientation of the chains, a wide range of cellulose derivatives was found to form both lyotropic and thermotropic chiral nematic liquid crystals . The selective light reflection, as well as the optical turbidity of the liquid crystalline cellulose derivatives solutions can be tuned, not only by the application of external fields [6,7], but also by the addition of aqueous salt solvents  and by playing with solvent/cellulose derivative systems [9,10,11]. The dynamic control of the cholesteric coloration and optical clarity of lyotropic aqueous cellulose derivatives was more recently achieved by using various N-alkyl-substituted methylimidazolium salts and a weak electric field [12,13]. The electro-optical behavior of the system was interpreted in terms of the salt-containing liquid-crystalline system and the medium viscous electrolytic and high resistance characteristics . In order to improve the optical characteristics of the solutions the treatment of surfaces, as well as the use of solvents that decrease the viscosity of the liquid crystalline cellulose solutions was investigated . Many efforts were done to trap the chiral nematic structure into iridescent solid films. Principal attempts refer the use of solvents that can undergo polymerization and also the use of UV sensitive substituents [15,16,17,18]. Lasing in solid cross-linked cholesteric cellulose based films with high reflectivity doped with fluorescent dyes was also recently evidenced in literature . The fabrication of cellulosic spheres by microfluidics, with iridescence was also described in literature . In addition to cellulose derivatives liquid crystalline phases it was also found that Nano crystalline cellulose (NCC) films were capable of reflecting colored light if prepared from liquid-crystalline cellulose suspensions. NCC liquid crystal templates were used to generate new photonic materials, which can combine mesoporosity with long-range chiral ordering [21,22]. Moreover the incorporation of NCC rods into composite materials results into systems with enhanced mechanical properties, which have been investigated systematically in literature . NCC rods seemed the perfect material to incorporate in cellulosic water-soluble matrices because of their intrinsic hydrophilic character . Many studies were performed and described in literature that concerns the preparation of films from NCC/polymer mixtures in aqueous media , more recently nano cellulose paper was applied as substrate and gate dielectric to produce flexible field effect transistors  and also electro-optical sensors .
In addition to that, sheared cellulose derivatives casted solid films, with a complex network of defects, which are easily identified by polarizing optical microscopy (POM), under cross polars, were also obtained and studied . Various reports were published in order to correlate the defects appearance and the rheological behavior of the precursor solutions but some fundamental questions are not yet answered (Figure 2). X-rays results showed that the cholesteric order can be destroyed in sheared films and that a bundle of warped helicoidal fiber-like structures where the cellobiose block spins around the axis of the fiber can develop. The bundles should have fibers with both the levogyre and dextrogyre arrangements, with equal probabilities, and have a residual orientation along the shear direction .
Atomic force microscopy (AFM) measurements revealed that sheared films topographical features could be affined by playing with the films processing conditions . It was demonstrated that the films prepared from liquid crystalline solutions can show two periodic structures, primary and secondary set bands. The former consisting of bands perpendicular to the shear direction while the latter has the bands slightly tilted from that direction. An out-of-plane angle variation of the sinusoidal molecular orientation was also reported [29,30]. The anisotropic nature of cellulosic solutions give them also unique characteristics that has impact, for example, in the way the viscosity changes with polymer concentration. For low polymer concentrations, while in the isotropic phase, the viscosity of the solutions increases with the increase of polymer fraction. However, for higher polymer concentrations, corresponding to the formation of the liquid crystalline phase, the increase in concentration results in a decrease of the viscosity. This was attributed to the spontaneous orientation of the mesogenic cellulose segments above the critical concentration . The viscosity drop, associated to the liquid crystalline phase appearance, is an important effect that one can take profit from when working with relatively high concentrated cellulose based solutions. The characteristics of the solutions make them suitable for preparing shear-casting films with unique characteristics that allowed the preparation of alignment layers to liquid crystals, as well as refractive gratings [24,27].
Electrospinning as well as cellulose acid hydrolysis (Figure 3) can be used to produce fibers from cellulose based liquid crystalline solutions, with diameters ranging from few nanometers to hundreds of microns, which can be at the origin of mats with very high surface areas . The most interesting result obtained from cellulosic liquid crystals by using the electrospinning technique, was the generation of jets and fibers with intrinsic curvature, which arise from stiff line defects (disclinations) that develop during processing. Due to the intrinsic curvature of the system micro-jets swinging as well as micro/nano fibers winding and overwinding, self-motions could be observed and controlled by adjusting temperature and electrospun experimental parameters. These cellulose-based materials not only mimic at the micro/nano scale the helical shapes observed, for example, in tendrils but also their motion and mechanical adaptability could be reproduced. The same mechanism was in action for all these systems providing that the same physical model, proposed for elastic filaments with intrinsic curvature, could be applicable. The cellulose-based non-woven mats produced were expected to play a significant role in the generation of nano- and microdevices, because of their capacities as separation media, actuators, and host materials for drug delivery [31,32,33].
In this work, we aim to review snapshots of research carried out on cellulosic-based liquid crystalline systems, which give insights into the relation between structure/properties on sheared casted films and fibers and networks of cellulose nanorods (not organized in an iridescent cholesteric structure)/Liquid crystal systems. In particular we will focus on the use of several techniques, which include solid state NMR, Rheo-NMR, MRI, X-rays, AFM, and mechanical essays. To illustrate the potential applications of the fibers and films produced from liquid crystalline cellulose networks we refer their use to build a soft sensitive moisture motor and electro-optical devices.
In order to understand the origin of the intrinsic curvature observed for cellulosic liquid crystalline materials, Magnetic Resonance Imaging (MRI) experiments were performed on different acetoxypropylcellulose (APC) dimethylacetamide (DMac) solutions. The synthesis of APC was performed according to the procedure previously described in . The MRI data were taken on a vertical wide bore 7.05 T Bruker 300 AVANCE III NMR spectrometer (Rheinstetten, Germany) according to . The studies were performed on cellulosic solutions that were sheared in capillaries with different diameters. The flow inside the capillaries and the jet at the end of them were observed. Depending on the shear rate and on the anisotropic characteristics of cellulosic solutions, the jet showed spontaneous curvature and torsion. MRI analysis allowed imaging of characteristic structure at chosen filament cross-sections along the capillary tube as can be observed in Figure 4.
Isotropic solutions confined in the capillary, which generate straight fibers on extrusion, showed a homogeneous symmetric cross-section structure (Figure 4A), implying that the averaging of differing structural features would maintain a straight fiber conformation. Confined solutions of cellulose in the cholesteric liquid-crystal phase, which generate curved fibers, showed a heterogeneous structure in cross-section with the hard “island” predominantly located closest to the tube walls and never in the middle of the tube. The off-axis position of the hard “islands” varies along the tube (Figure 4B,C). POM confirmed that the hard “islands” correspond to the core of a linear topological defect (disclination) that can be observed in anisotropic pre- sheared solutions above a certain critical shear rate (Figure 5). POM images show that the defects lines are forming a helix along the capillary tube. This observation is supported by the MRI measurements indicates that from one layer to the following the hard objects rotate (in Figure 4 an anticlockwise rotation can be seen). The MRI image contrast reflects the local mechanical stiffness of the material, so that dark regions represent hard “islands” on each cross-section, with the average diameter from 25 to 50 μm, which is much lower than the capillary diameter (R*) and similar to the average diameter of the helices measured in POM images.
The present results show that liquid crystalline disclinations are at the origin of the intrinsic curvature observed for jets and electrospun fibers obtained from cellulosic mesophases. The intrinsic curvature of the fibers, responsible for their curl and twist, arises from an off-axis core line defect disclination which is present when the fibers were prepared from liquid crystalline solutions. The consequence of the intrinsic curvature of the system was also observed during thinning and break-up of jets produced by continuous motion of anisotropic solutions. The spirals and helices found at micro/nano scale mimic the shapes observed, for example, in hair  and tendrils  due to a similar intrinsic curvature dominated mechanism, providing that, for all these systems, the physical model proposed for elastic rods with intrinsic curvature could be applicable. The fine-tuning of temperature will allow us to control the non-woven self-winding mats’ ability adjusting their surface-to-volume ratio, due to the intrinsic curvature of constituent fibers, which opens horizons for fabricating new natural scaffolds for tissue engineering .
The characterization of precursor cellulosic solutions was found to be crucial to understand the relation between properties and structure. In order to perform this goal, Rheo-NMR techniques have been used in the study of liquid crystalline cellulosic solutions under shear  and relaxation  while NMR spectroscopy was applied to the study of the corresponding films and fibers . These studies allowed for the characterization of the molecular order and structure in these systems, yielding information not directly accessible to other techniques as light scattering  or Xray diffraction .
A Rheo-NMR study [42,43] on the model system hydroxypropylcellulose + deuterium oxide (HPC + D2O) at 50% by weight concentration showed a rich and complex behavior both under shear and in relaxation as can be observed from the deuterium spectra recorded in both processes and shown in Figure 6 for selected shear rates.
It was found under shear that depending upon the shear rate the system goes from a regime of tumbling cholesteric domains [44,45] observed at low shear rates = 0.1 s−1 where the system order is low, to a regime of director flow alignment with partial or total helix suppression for shear rates of the order of 1 s−1 or above. The three distinct flow regimes introduced by Onogi and Asada  in the context of shear flow of LC polymers were directly identified in the Rheo-NMR  results and were ascribed to the tumbling of cholesteric domains, the partial flow alignment of the director and helix deformation and the director flow alignment with partial or total helix suppression. Relaxation data in the different regimes show that the system moves towards the reformation of the cholesteric domains and depending upon the starting point where the system is left in to relax this process may be more or less involved. When relaxation initiates from the tumbling cholesteric domains regime the cholesteric domains grow and possibly accrete giving rise to an immediate increase in order. When relaxation initiates from the flow director aligning regime, cholesteric helices start to form from the aligned director state, producing a significant decrease in order that only reverts when the reformed cholesteric domains start to accrete and grow, a process that takes significantly longer times to develop.
This study was carried out through the analysis of the deuterium spectra arising from the D2O molecules and shown in part in Figure 6. The spectra showed the presence of a single population of D2O molecules experiencing a large motional averaging. The deuterium spectra were analysed and simulated considering the presence of water rich regions (WRR) imbedded with the polymer chains and the presence of fast molecular diffusion within these WRR that allow the D2O molecules to sample the order of the neighbouring polymer chains. Based on those results, and the accumulated knowledge on this system , it was possible to identify five different mesoscopic states reached by the HPC/water system during shear and relaxation as shown in Figure 7. State I is the partially aligned cholesteric polydomain state obtained after relaxation from shearing with low shear rates. State II is the cholesteric polydomain state attained after relaxation from shearing with high shear rates. State III is the tumbling regime of the cholesteric domains obtained with low shear rates, state IV is the partial flow alignment state associated with the intermediate shear rates, and state V is the flow aligned nematic obtained at high shear rates. The up arrows indicate the relaxation path while the down arrows indicate the path under shear starting from the polydomain cholesteric reached in the preparation state. This picture is in direct correspondence with the three regions of steady shear flow introduced by Onogi and Asada , state III appears at low shear rates and corresponds to the tumbling regime, the intermediate region corresponds to state IV and state V is associated with the high shear rate region.
In a recent NMR study , bulk samples, thin films and electro spun fibers of the cellulosic composite formed by liquid crystalline acetoxypropylcellulose (APC) and deuterated nematic 40-pentyl-4-cyanobiphenyl (5CB-αd2) with the percentage of 85% APC by weight were characterized by deuterium spectroscopy in terms of molecular orientational order. Deuterium spectra obtained in thin films and bulk samples show similar temperature dependences as the one found in spun fibers and shown in Figure 8.
It was found that the low molecular weight liquid crystal is phase separated from the APC and concentrates on submicron droplets in the three types of samples. These droplets are seen to develop a nematic wetting layer at the APC-5CBαd2 interface that experiences an order-disorder transition driven by the polymer network N-I transition. Simulation of the deuterium powder patterns as a function of temperature has shown that the APC network I-N transition exhibits a pronounced subcritical behavior within a heterogeneity scenario.
This study relied on the analysis of the deuterium spectra arising from the 5CBαd2 molecules as they diffuse inside the submicron size droplets, sampling both their isotropic core, as well as the polymer surface induced nematic layer. A Landau-de Gennes modelling of this induced order allowed the order profile inside the droplets to be determined as a function of the surface order SS imposed by the polymer chains, enabling the simulation of the ordered part of the deuterium spectra shown in Figure 7. At the network I-N transition a significant coexistence of both isotropic and ordered components in the deuterium spectra indicates the presence of heterogeneity in the network. To model the network order parameter temperature dependence and the network heterogeneity, a Landau de Gennes modeling of the network order was considered with a Gaussian distribution in the isotropic phase super cooling limit temperature T* . This modeling allowed the full fitting of the spectra shown in Figure 8 and the determination of the SS temperature dependence shown in Figure 9.
The SS temperature dependence shows that the network is subcritical and the spread in transition temperatures of around 7 K for each of the three samples studied indicates the presence of heterogeneity in the APC + 5CBαd2 system .
Cellulosic liquid crystalline networks obtained from the previous studied systems can be at the origin of promising soft matter devices . In order to characterize these type of networks, Wide Angle X-ray Scattering (WAXS) studies were performed  namely of crosslinked APC films produced from chiral nematic solutions . The studies were carried on films subjected or not to a uniaxial stress. The results indicate that the films are constituted by a bundle of helicoidal fiber-like structures, where the cellobiose block spins around the axis of the fiber. Without the stretch, these bundles are warped, only with a residual orientation along the casting direction. The stretch orients the bundles along it, increasing the nematic-like ordering of the fibers. Under stress, the network of molecules that connects the cellobiose blocks and forms the cellulosic matrix tends to organize their links in a hexagonal-like structure. The X-ray diffraction patterns of the free standing, unstretched, cellulose films present three diffraction peaks, anisotropically disposed around the z-axis, as shown in Figure 10. In Figure 11a,b, the diffracted intensity is plotted as a function of q (scattering vector), along the x and y axes directions. The diffraction peaks in the curves Ixq were fitted with Lorentzian functions to find the characteristic distances (d) and full-widths at half- height (W).
The characteristic distances associated to the peaks are d1 = (1.13 ± 0.02) nm; d2 = (0.44 ± 0.01) nm; and d3 = (0.50 ± 0.01) nm. In a previous work  only peak 1 was observed due to the limited range of scattering wave vectors investigated. The correlation lengths D = λx/(W·cosθ) calculated are D1 ≈ 3 nm; D2 ≈ 2 nm; and D3 ≈ 14 nm.
The analysis of the diffraction peaks in the x–y plane indicates that peaks 1 and 2 are more intense along the x direction, which corresponds to the direction perpendicular to the casting. On the other hand, we could not fully verify if peak 3 is also anisotropic with respect to the z-axis since the presence of peak 2, particularly along the x-axis direction, prevents a reliable azimuthal analysis of it. Nevertheless, visual inspection of Figure 10 seems to indicate that this peak is preferentially located in the direction perpendicular to the casting direction. The azimuthal angle analysis of the diffracted intensity (angle , measured in the xy plane, starting from the x-axis, in the counter clockwise direction) of the peaks allowed us to obtain the orientational order parameters (OP) .
Concerning the case where the film is subjected to a uniaxial stress parallel to the casting direction (Figure 12). We did not observe significant differences in the patterns obtained in the different film locations of the X-ray exposures, indicating, at least, in our experimental conditions, homogeneity of the film.
As the stress increases, the order parameters of the three peaks increase, reaching values at the maximum stress applied (y = 0.40) of OP1 = (0.85 ± 0.03); OP2 = (0.43 ± 0.02); and OP3 = (0.82 ± 0.01). This increase in the orientational order parameter of peak 1 is consistent with the results obtained in . Figure 13 shows the diffracted intensity as a function of q along the x (Figure 13a) and y (Figure 13b) axis directions. As the stretch is increased, peak 3 become more and more defined in the diffracted intensity versus q curves (Figure 13b). The positions of the peaks were not modified by the stress. An intriguing result was obtained when we analyzed peak 2 profile as a function of the azimuthal angle (Figure 13c).
A hexagonal distribution of diffraction maxima could be identified in the peak 2 position, which provided a hexagonal lattice parameter dH ≈ 0.5 nm about the same of the characteristic distance d3. The value of dH was obtained assuming that the diffraction peaks of hexagonal symmetry observed in the position of peak 2 (d ≈ 0.44 nm) correspond to the (100) diffraction plane of the two-dimensional hexagonal packing, i.e., dH = d100/(cos(π/6)). The typical dimension of an extended glucose molecule is of the order of 0.5 nm and the cellobiose, composed by two glucose molecules, is the repeating building-block in the cellulosic sample. The structure proposed for the cellulosic film has to take into account the diffraction characteristic distances observed, the dimension of the cellobiose building block, and the information that, before the casting, the system presents a cholesteric structure. We propose that in the film there is a bundle of helicoidal fiber-like structures where the cellobiose block spins around the axis of the fiber. The distance between the fibers should be of the order 1.1 nm, corresponding to peak 1 of the diffraction pattern. Since there is no evidence of chiral activity in the cellulosic films in the macroscopic scale, these bundles should have fibers with both the levogyre and dextrogyre arrangements, with equal probabilities. Without the stretch, these bundles of fibers may be warped, only with a residual orientation along the casting direction. The stretch orients the bundles along it, increasing the nematic-like ordering of the fibers. Under stress, the network of molecules that connects the cellobiose blocs and forms the cellulosic matrix tends to organize their links in a hexagonal- like structure.
The same samples used to perform the WAXS essays were used to perform POM essays. The optical microscopy texture of the sample under crossed polarizers (casting direction parallel to the analyser) revealed that the film is birefringent, but with a non-uniform texture (Figure 14a).
The analysis of the texture under crossed polarizers leads to the macroscopic arrangement of the director sketched in Figure 14b. There are light and dark regions that form a pattern with stripes, with a periodicity of ≈ 4.4 μm (distance between three light regions), perpendicular to the direction of the casting. This periodic structure is originated by the shear-casting procedure. After the cast the molecular chains have a collective relaxation that results in the formation of that pattern. This morphology has been observed in other cellulose derivative films and was found to be influenced by the precursor solution composition, solvent evaporation rate, film thickness, and rate and duration of shear [28,49]. The application of successive stretches in the direction of the casting (i.e., in this experimental configuration, parallel to the analyser direction) showed that the texture of the film becomes increasingly dark. This is because the direction of the optical axis, previously created by the casting, is parallel to the analyser direction. If the optical axis of the sample is rotated by 45° in the plane of the microscope plate, the texture became bright. This result is consistent with the nanoscopic structure proposed in the previous X-ray scattering section. The fiber-like structure where the cellobiose block spins around the axis of the fiber defines the director direction, parallel to the casting direction. As the X-ray beam probes a large portion of the sample (typical beam diameter of about 1 mm) the diffraction pattern reveals the mean orientation direction of the director. Upon relaxation (initially at = 0.29 and after tR = 5 min) the film did not recover the initial texture, in accordance with the X-ray results already discussed.
When the stretch is applied perpendicular to the casting direction the texture of the sample under crossed polarizers (Figure 14e,f) becomes increasingly darker with increasing stretch, and then clearer after its relaxation (Figure 14g). Assuming the structure depicted in Figure 14b, the stretch along the direction perpendicular to the casting will impose a tendency of reorientation of the fiber-like arrangement parallel to the stretching direction. This reorientation may in principle proceed either in the clockwise or the anticlockwise direction but due to the initial oscillatory form of the director around the casting direction due to the band structure, different regions will rotate in opposite sense depending on the initial director orientation at each point. Depending on the location of the film analyzed and the boundary conditions imposed by the borders of the film, the fibers will tend to reorient to their local environment. This fact can explain the different X-ray patterns obtained in different film positions (Figure 15). At the border of the film (positions A and B in Figure 15) the director, that was initially oriented on average parallel to the casting direction (x-axis), is now primarily oriented at ± π/4 with respect to the x-axis due to the boundary conditions that prevent a complete rotation of the director to the stretching direction. In the center of the film (position C in Figure 15), the director is oriented primarily along the y-axis (stretching direction). Let us look in more detail at the appearance of the film under stress, without the crossed polarizers. The film initially had 2 mm in length (L0), 5 mm in width and 21 μm in thick and was stretched every 6 min until 16 mm in length, and then relaxed.
Figure 16 shows the sequence of stretches of the film from = 0.71 (Figure 16b) until = 7 (Figure 16d), with the stress applied perpendicular to the casting direction. It is clearly observed an additional periodicity in the direction perpendicular to the casting direction.
The distance (along the x-axis) between two successive stripes increases linearly with (Figure 17). Under crossed polarizers these stripes are also birefringent (Figure 18). This result indicates that the effect of the casting in the macroscopic structure of the cellulosic film is not only to impose a periodic bend organization of the local director, as sketched in Figure 14b in its direction, but also bends this super structure in the direction perpendicular to it in a larger length scale. Upon relaxation, the film takes a long time to recover its original length (Figure 16e,f). However, its shape is strongly modified, in particular its width (direction perpendicular to the stretch), indicating the plastic behavior of the deformation.
When the film is stretched in the direction parallel to the casting direction this additional periodicity is not observed.
To perform the Atomic Force Microscopy (AFM) experiments, solutions of cellulose derivatives at several concentrations, ranging from the isotropic to the anisotropic phase region, were prepared.
Figure 18 shows the 3D topography image (20 × 20 μm2 scan) of the free surface of a sheared HPC film prepared from a 60% w/w solution at a shear rate v1 = 5 mm/s. The image shows two different scale ranges: a primary set of “large” bands, perpendicular to the shear direction, and a smoother texture characterized by a secondary periodic structure containing “small” bands.
Figure 19 shows a top view image of the height scan of the surface shown in Figure 18 and the analysis of the height profile at two cross sections: AA' and BB'. Cross section AA' was taken along the shear direction. The periodicity of the “large” bands, l1, and the average peak-to-valley height for these bands, h1, were determined from the AA' height profile plot, as indicated. Cross section BB' was taken along the direction of the secondary periodic “small” bands. The periodicity of the “small” bands, l2, and their peak-to-valley height, h2, were measured from the BB′ height profile plot, as indicated. The arrows on the top of the view image along AA' and BB' lines mark the points used for the measurements performed in the height profile plots.
Figure 20 shows the top view image of the amplitude scan of the free surface of three sheared HPC films prepared at a shear rate of v1 = 5 mm/s from solutions of different concentrations: (a) 30% (w/w), (b) 50% (w/w); and (c) 65% (w/w). The surface of the film prepared from 30% (w/w) does not possess any periodicity. A primary and a secondary set of bands were observed only on the films prepared from anisotropic solutions, i.e., 50%–65% (w/w). Moreover, the films prepared from the solutions of the same concentration, using a higher shear rate v2 = 10 mm/s), exhibit similar topographies, but they are characterized by different parameters. At a constant concentration, for example at 65% (w/w), the periodicity of the bands (l1) shows a tendency to decrease when the shear rate increases (l1(v1) = 2.97 μm and l1(v2) = 1.97 μm). At a constant shear rate, as the concentration of the polymer increases, the periodicity of the bands decreases (for v1, at 50% and 65% (w/w), l1 = 4.68 μm and l1 = 2.97 μm, respectively).
A tuneable topographic system may be obtained from HPC aqueous liquid crystalline solutions . The results point out that two kinds of periodicities may be locked and adjusted in these systems as a function of the processing conditions. The set of “large” bands, which develops perpendicular to the shear direction, can be described as a relaxation process, which occurs immediately after the end of a shear applied to polymer liquid-crystalline solutions and attributed to contraction strains of the sheared sample induced by stress relaxation after cessation of flow. The secondary bands periodicities show a net tendency to decrease with polymer content, which seems an indication that the development of the “small” bands are mainly ruled by the cholesteric liquid crystal characteristics imposed by the initial precursor solutions. The pitch of the precursor chiral nematic solution and the related values of the liquid crystal elastic constants of the material can therefore be mainly responsible for the variation in size of the secondary bands, observed experimentally . The films are found to be self-affine between 300 nm and 4 μm but not for higher scales. In general, the fractal dimension is found to increase with both polymer concentration and shear rate. This trend reflects the increasing complexity of the surface topography when the films are prepared with higher polymer concentrations or with higher shear rates .
Anisotropic solid films were fabricated by spreading the HPC anisotropic solutions, 60% (w/w), with the help of a calibrated shear casting knife, at room temperature, in an appropriate Teflon mould, this procedure allows the precise control of the shear casting flow speed (v) (1 mm·s−1) and enables the ready removal of the films without damaging at room temperature, other methods to obtain sheared HPC solid films involved higher processing temperatures . After solvent controlled evaporation, the solid cast shear films had an average thickness between 14 and 30 μm. As evaporation continues, the density of rod-like fragments increases near the free top surface, giving rise to increased orientational order. This in turn causes elongation at the top of the film in the direction parallel to the director, and since the dimensions of the bottom surface in contact with the glass substrate are fixed, the top surface buckles, forming a set of grooves shown previously [52,53,54].
The modulus of the cellulose network has been measured for strain along the director, as well as perpendicular to it. Results are shown in Figure 21; for small strains, Young’s modulus is 263 ± 39 MPa for shear parallel and 140 ± 9 MPa perpendicular to the director. Above a threshold of 4 MPa, the stress in the perpendicular direction is nearly independent of the strain. This “semi-soft” elastic response is characteristic of liquid crystal elastomers  and has been associated to a director reorientation. However, as already highlighted , a reset of order can also be the underlying mechanism for this process as observed in sheared anisotropic cellulosic films . The film rupture is preceded of a plastic regime when stretching is imposed parallel to the casting direction while it is preceded of significant necking during the “semi-soft” elastic response when stretching is imposed perpendicular to the casting direction.
When exposed to water vapor, free standing films prepared from a 60% (w/w) solution bend, as shown in Figure 22. When water vapor penetrates the free surface of the film, the sample bends around an axis parallel to the shear direction, with the free surface on the outside (Figure 22a). This is consistent with expansion of the free surface of the film in the direction perpendicular to the director. Such an expansion is expected, since the order parameter is reduced by the presence of the solvent water, and furthermore the presence of water molecules between the cellulose chains in the rigid segments is expected to cause the thickness of the rod-like fragments to increase.
The shear stress associated with such bend has been measured, as a function of time (Figure 23), in a 20 mm × 20 mm × 32 μm planar sample at 24 °C with free surface exposed to humidity. Measurements were taken with Mettler Toledo AG204 load sensor. The maximum stress measured was 383 Pa.
When the film is allowed to dry, either by heating or by being placed in a low-humidity environment, the film unbends, reversibly assuming its original shape. The bending is relatively fast, on the scale of ≈1 s.
Interestingly, when the glass side of the film is exposed to water vapor, it bends around an axis perpendicular to the shear direction, with the glass side being convex (Figure 22b). This is consistent with a nearly isotropic expansion of the glass side surface due to the presence of moisture. Since corrugations on the free surface give rise to a smaller effective modulus for bend in this direction, as has been confirmed by independent measurements, bend occurs around an axis perpendicular to the shear direction. The bend produced by exposing the glass side to water vapor is considerably smaller than that of the free surface. Taking advantage to the bending moisture effect a soft cellulosic motor was built (Figure 24) .
Nano crystalline cellulose rods can be incorporated into composite materials, enhancing their mechanical properties . NCC filler was used as a probe, which can influence the mechanical properties of the films but does not destroy the liquid crystalline characteristics of the composite material. In fact, adding 0.1% of NCC rods implies that the Young’s modulus of the films, as well as the tensile strength, measured in perpendicular (Per) and parallel (Par) directions to the casting, were increased by a factor of 2.5 and 3.2 for Par and 3.0 and 2.2 for Per, respectively, when compared with films prepared from HPC anisotropic solutions . Because of the high degree of molecular orientation, the HPC and the HPC/NCC films exhibit high modulus and strength along the shear direction and the mechanical strength in the transverse direction is low. These anisotropic mechanical properties are consistent with the molecular orientation, which results from the flow of the liquid crystalline solution under shear stress. The fact that the Young’s modulus and strength is much higher for HPC/NCC compared with HPC films, along the shear direction, is an indication that NCC rods align along this direction when the films are prepared. NCC rods enhanced the brittle behavior along this direction, as well as in the Per direction and act as a stiffener to the anisotropic cellulose matrix, which is also reflected in the strength deformation values for Par and Per directions.
The features (not the values) of the stress/strain curves obtained were similar to those from other APC and HPC already reported in the literature for isotropic and anisotropic cellulose derivatives [59,60,61].
Cellulose derivatives composites for electro-optical (EO) applications were introduced in 1982 by Craighead et al. , followed a few years later by a different type of cellulose derivative EO cell, named cellulose-based polymer dispersed liquid crystal (CPDLC) [63,64]. Due to the good match between the ordinary refractive index of the nematic liquid crystal (NLC) E7 (1.510) and the refractive indexes of HPC (1.49), a very clear ON state is achieved when an electric field Eon is applied to the devices as can be seen in Figure 25.
The CPDLC cell was composed of a rough cellulose derivative polymeric film surrounded by two NLC layers and the set placed in between two transparent conducting rigid or flexible substrates. These thin solid films were prepared from cellulose derivatives solutions, casted, and sheared simultaneously by moving a calibrated Gardner knife at 1.25 mm·s−1. The films were allowed to dry at room temperature and kept in a controlled relative humidity (20%) chamber until further use. To evaluate the EO properties of these devices, the EO characterization was carried out using a laser-equipped optical bench in association with a function generator, a voltage amplifier, and a diode detector. The laser light was perpendicular to each sample and upon crossing it was collected at the diode detector whose output was fed to an amplifier and later recorded with a digital storage scope. All measurements were performed at room temperature. These cells showed very challenging properties, presenting high transmission coefficients values (around 0.8) in the ON state, but exhibiting turn-ON fields around 1.5 V/µm, giving rise to rather high turn-on voltages . Later on, a light scattering EO device where layers of two different cellulose derivatives were deposited as nonwoven nano and microfiber mats onto the conductive substrates by electrospinning, were presented . These devices can be used as high efficiency light shutters or as privacy windows since they can be electrically controlled to scatter light (OFF state) or to transmit it (on state) . These last devices presented an innovative method of preparing cellulose-based light scattering devices, which led to a major improvement in their EO properties and also their production cost. Using cellulose-based nano and microfibers mats as a network, EO light-scattering devices were produced as polymer-stabilized liquid crystal-type devices. In these devices, the cellulose derivatives were deposited as nonwoven nano- and microfiber mats onto the conductive substrates by electrospinning, and the cell was filled up by capillarity with a NLC. In these optical shutters, the LC is embedded with the fibers as a continuous phase, maximizing the LC/polymer surface contact and thus promoting improved EO properties. An increase in the on transparency and a marked decrease in the operating voltage of these devices were observed as the consequences of the improved interaction of the NLC with the nano and microfibers. More recently, a new type of EO device with improved EO properties was presented taking advantage of the high surface area of nanoscale cellulose whiskers .
On this later technology, cellulose-based LC EO devices were prepared by stacking between two transparent conductive oxide–coated glasses, two layers of a nematic LC having in between a thin film composed of nano crystalline cellulose rods. The major step forward in the EO properties of this type of device is the significant reduction of the turn ON electric field and the decrease in the response time to reach the ON state as can be seen in Figure 26.
The cholesteric nature of the cellulose derivatives liquid crystalline solutions gives rise to a complex rheological behavior and consequently has a fundamental impact on the properties of the films and fibers produced from these anisotropic solutions by different methods where different levels of shear are involved. Formation of helices in electro-spun fibers and the curling of cast planar films stem from the complex nature of the molecular packing imposed by the preparation induce shear on the precursor solutions. These features impart specific mechanical and optical properties to the cellulose derivatives fibers and films that make them high interest materials for photonics, microelectronics and related applications, as well as for build soft stimuli responsive devices.
The authors acknowledge financial support from Portuguese Science and Technology Foundation through grants: PTDC/CTM-Pol/1484/2012, PTDC/FIS/110132/2009, PEst-OE/FIS/UI0261/2011, PEst-C/CTM/LA0025/2013-14.
The authors declare no conflict of interest.
Maria Helena Godinho, Pedro Lúcio Almeida and João Luis Figueirinhas planned, wrote the manuscript and contributed equally to this work.