Cellulose whiskers (CWs) obtained from naturally occuring cellulose are nano-inclusions which show a lot of promise as mechanical reinforcements in polymers. Typically, a relatively high content is added to realize improvement in effective mechanical behavior. This enhancement in modulus is usually followed by a modest increase in strength but generally the ductility and toughness decrease. Our approach is to use small concentrations of CWs so as not to detrimentally affect processability, toughness and ductility. By aligning the small concentrations, we target the same kind of improvement in modulus and strength as reported in the literature, but at much smaller volume contents. In this work, we investigate the effect of AC electric field on the alignment of dispersed nanoscale CW in a polymer. Polyvinyl acetate (PVAc) is used as the model polymer because of the good interaction between CWs and PVAc. A low concentration of 0.4wt% was used for the study. Two dispersion methods, namely basic and modified, were developed. The basic method led to micron scale dispersion. Using the modified method, CWs were individually dispersed in PVAc with average lengths and diameters of 260 nm and 8 nm respectively yielding an aspect ratio of approximately 30. The behavior of CWs (alignment and chain formation) under an applied electric field was found to be a function of applied electric field magnitude, frequency and duration. Following alignment, the CW/PVAc nanocomposites are thermally dried in the presence of electric field to maintain the aligned microstructure. Improvements in dielectric constant and mechanical properties were observed for the aligned cases as compared to random case and pure PVAc. The optimal electric field magnitude, frequency and duration for the alignment and chain formation were found to be 200Vpp/mm, 50 KHz for duration of 20 minutes for the microcomposite and 250Vpp/mm, 10KHz for a duration of 1hr for the nanocomposite. At 0.4wt% concentration, 21% increase in dielectric constant for the optimal nanocomposite case. Above Tg, a 680% improvement in elastic modulus at 0.4wt% concentration for the optimal nanocomposite case. The reason for the significant reinforcement is attributed to alignment (rotation and chain formation) and chain-chain interaction (3D network formation and hydrogen bonding).

Raman spectroscopy has been used to monitor the deformation of natural cellulose whisker polymer nanocomposites. Cotton and tunicate whiskers were used as reinforcements in polymer matrices. Raman spectra from the nanocomposites highlight an intense band located at the 1095 cm-1 position. This band is reported to shift towards a lower wavenumber under the application of tensile deformation. On the other hand, the compressive deformation of the composite gives rise to an increase in the position of this Raman band. The shifts correspond to the direct deformation of the molecular backbone of cellulose, which is dominated by a C-O stretching mode. The Raman band located at 1095 cm-1 is shown to shift non-linearly before it reaches a plateau due to the breakdown of the whisker-matrix interface. The initial shift rate is associated with the stiffness of the cellulose whiskers. The stiffnesses of single whiskers of cotton and tunicate are found to be 58 and 155 GPa respectively, assuming two dimensional (2D) in-plane distribution of whiskers. Cyclic deformation tests of the composites provide an insight into understanding the behaviour of the whisker-polymer matrix interface under tension and compression. It is found that residual compressive stress occurs during each cycle of the deformation. The level of disruption at the whisker-matrix interface is determined by estimating the energy dissipation, which is proportional to the hysteresis area. Local orientation is also observed in the nanocomposites produced by solution casting and subsequent melt pressing. Dark regions of the composites viewed under a polarised optical microscopy are found to represent areas in which the cellulose whiskers form a randomly oriented whisker network. A shift rate for the Raman band initially located at 1095 cm-1 obtained in the dark regions of 12.2 vol% tunicate whisker poly(vinyl acetate) nanocomposites is found to be -0.5±0.07 cm-1%-1, which is lower than -1.2±0.04 cm-1%-1 from the bright regions. Exposure to water and temperature during the deformation of the nanocomposites results in significant changes in stress transfer between the whiskers and the matrix. It is shown that the interface can be 'switched-off' for the poly(vinyl acetate)/whisker system in the presence of water and also at temperature above the glass transition.

This research explored the processing and properties of PNCs using a polyfurfural alcohol (PFA) matrix. The precursor for PFA, furfuryl alcohol (FA) is sourced from feedstocks rich in hemicellulose, such as corn cobs, oat hulls and wood. To exploit FA as a polymerizable solvent, cellulose whiskers (CW) and montmorillonite clay (MMT) were used as the nanoparticle phase. Results from PNC processing show that CW and MMT can be dispersed in the PFA matrix by means of insitu polymerization, without the use of surfactants or dilution in solvents. Both CW and MMT nanoparticles catalyze the polymerization of furfuryl alcohol (FA). Moreover, the insitu intercalative polymerization of FA in the interlayer galleries of MMT leads to the complete exfoliation of the MMT in the PFA matrix. CW and MMT both function as effective matrix modifiers, increasing the thermal stability of PFA nanocomposites compared to pure PFA polymer. The increased thermal stability is seen as significant increases in the onset of degradation and in residual weight at high temperature. This research also explored the surface functionalization of Cu, Ni and Pt substrates by self-assembly of a range of difunctional linker molecules. Characterization by XPS and PM-IRRAS indicate that diisocyanides and dicarboxylic acids both form chemically "sticky" surfaces after self-assembly on Cu and Ni. Sticky surfaces may provide a means of increasing nanoparticle dispersion in metal nanocluster filled PNCs, by increasing their interaction with the matrix polymer. Another potential application for sticky surfaces on Cu is in the ongoing miniaturization of circuit boards. The functionalization of Cu bond pad substrates with linker molecules may provide an alternate means of bonding components to their bond pads, with higher placement accuracy compared to solder bumps.

Marine ecosystems can be a promising reservoir of various kinds of chemical components, applicable as pharmaceutical materials, food, cosmetics, nutraceuticals, and others for different industry. As an example, Tunicates, a group of marine animals, have been attracted a lot of attention in medical application, food market, water pollution issues, and Cellulose nanomaterial production due to their consisting of chemical compounds such as cellulose, amino-sugars, and proteins or protein-polysaccharide complexes e.g. collagen, glycosaminoglycan, chitin, scleroprotein, iodine-binding proteins, and elastin. In this project,  two dominant species of Scandinavian Tunicates, i.e. Ciona intestinalis and Clavelina lepadiformis, harvested from Norwegian ocean have been classified according to body sizes, depths from the ocean surface, ages and species, and separated physically into outer layer and internal organs, followed by measurements of sugar composition, oil content, and  protein content. Application potentials have been investigated by trials for production of pure crystalline cellulose, bioethanol, and biodiesel, and by analysis of amino acid composition of the samples. The cellulose percentage and cellulose yield for the chemically pure cellulose obtained, is around 96% and 54% respectively, and the protein content is decreased step by step by the acid, alkali, and bleaching process applied. Bioethanol can be obtained by fermentation of tunicate hydrolysate with strains A and C which are derived from Saccharomyces cerevisiae. The biodiesel yield of tunicate samples is around 4-6% as an average. The amino acid compositions in our tunicate samples are similar to egg albumin, implying tunicate being an alternative material for animal feed production. Several processing treatments have been conducted with the aims to fractionate tunicate biomass components or enhance the cellulose accessibility and reactivity. After a single processing step, Ba(OH)2 treated samples seemed to be the best in terms of both cellulose preservation (66.5% cellulose) and protein removal (6% protein in the treated residue). Results from the physical separation plus washing reveal that the highest amount of cellulose and protein presents is found in the outer (Tunic) part and internal organs of Tunicate samples respectively. Data obtained from FTIR(Fourier Transform Infrared Spectroscopy) and SEM(Scanning Electron Microscope) indicate that among all processing trials, H3PO4 is the most effective in decreasing the cellulose crystallinity, which renders a higher accessibility for acidic or enzymatic reaction during bioethanol production due to a higher amount of amorphous structure of cellulose. From the analysis results of component contents and structures, it could be concluded that increase of deepness results in a decrease of sugar content of the Tunicate samples while there are no differences in protein and carbohydrate content in different tunicate species. The body size has a positive influence on the protein content and the sample age alters the contents of both sugar and protein. In addition, Tunicate oil has high phospholipid content instead of glycerol ester, the latter being the common oil from vegetable origins. Moreover, lots of free fatty acid is present, and the composition profile of Tunicate fatty acids seems to be similar to fish oil, as revealed by NMR (Nuclear Magnetic Resonance Spectroscopy), FTIR, and GC-MS (Gas Chromatography-Mass Spectrometry).

Marine ecosystems can be a promising reservoir of various kinds of chemical components, applicable as pharmaceutical materials, food, cosmetics, nutraceuticals, and others for different industry. As an example, Tunicates, a group of marine animals, have been attracted a lot of attention in medical application, food market, water pollution issues, and Cellulose nanomaterial production due to their consisting of chemical compounds such as cellulose, amino-sugars, and proteins or protein-polysaccharide complexes e.g. collagen, glycosaminoglycan, chitin, scleroprotein, iodine-binding proteins, and elastin. In this project,  two dominant species of Scandinavian Tunicates, i.e. Ciona intestinalis and Clavelina lepadiformis, harvested from Norwegian ocean have been classified according to body sizes, depths from the ocean surface, ages and species, and separated physically into outer layer and internal organs, followed by measurements of sugar composition, oil content, and  protein content. Application potentials have been investigated by trials for production of pure crystalline cellulose, bioethanol, and biodiesel, and by analysis of amino acid composition of the samples. The cellulose percentage and cellulose yield for the chemically pure cellulose obtained, is around 96% and 54% respectively, and the protein content is decreased step by step by the acid, alkali, and bleaching process applied. Bioethanol can be obtained by fermentation of tunicate hydrolysate with strains A and C which are derived from Saccharomyces cerevisiae. The biodiesel yield of tunicate samples is around 4-6% as an average. The amino acid compositions in our tunicate samples are similar to egg albumin, implying tunicate being an alternative material for animal feed production. Several processing treatments have been conducted with the aims to fractionate tunicate biomass components or enhance the cellulose accessibility and reactivity. After a single processing step, Ba(OH)2 treated samples seemed to be the best in terms of both cellulose preservation (66.5% cellulose) and protein removal (6% protein in the treated residue). Results from the physical separation plus washing reveal that the highest amount of cellulose and protein presents is found in the outer (Tunic) part and internal organs of Tunicate samples respectively. Data obtained from FTIR(Fourier Transform Infrared Spectroscopy) and SEM(Scanning Electron Microscope) indicate that among all processing trials, H3PO4 is the most effective in decreasing the cellulose crystallinity, which renders a higher accessibility for acidic or enzymatic reaction during bioethanol production due to a higher amount of amorphous structure of cellulose. From the analysis results of component contents and structures, it could be concluded that increase of deepness results in a decrease of sugar content of the Tunicate samples while there are no differences in protein and carbohydrate content in different tunicate species. The body size has a positive influence on the protein content and the sample age alters the contents of both sugar and protein. In addition, Tunicate oil has high phospholipid content instead of glycerol ester, the latter being the common oil from vegetable origins. Moreover, lots of free fatty acid is present, and the composition profile of Tunicate fatty acids seems to be similar to fish oil, as revealed by NMR (Nuclear Magnetic Resonance Spectroscopy), FTIR, and GC-MS (Gas Chromatography-Mass Spectrometry).

L’objectif de cette étude est la réalisation de séparateurs de batterie haute performance par extrusion. Ces électrolytes polymères solides nécessitent d’être perméables au courant ionique mais aussi isolants électrique, tout en étant résistants mécaniquement. Une des possibilités étudiée pour le renfort mécanique est la dispersion de charges nanométriques (whiskers de cellulose) dans un polymère. Les whiskers de cellulose sont des bâtonnets cristallins d’une longueur entre 100 et 300nm et d’un diamètre entre 5 et 20 nm. Lorsque ces charges sont dispersées de façon homogène, elles forment un réseau percolant, améliorant de cette façon le renfort mécanique de la matrice pour de faibles concentrations. Le but est donc de réaliser cette dispersion dans un polymère fondu par extrusion, en comparaison avec le procédé bien établi d’évaporation de solvant. Les difficultés principales viennent de l’agglomération des whiskers de cellulose via des liaisons hydrogènes et du milieu très concentré dans lequel ces charges doivent être dispersées. Ainsi, la première partie de l’étude est de déterminer le processus de préparation des whiskers de cellulose, limitant l'agglomération et permettant d’obtenir une suspension stable. Ce système stable est nécessaire pour la formation d'un réseau par évaporation de solvant. Une fois le protocole optimisé, la deuxième partie de l’étude porte sur la dispersion de ces whiskers dans la matrice fondue au mélangeur interne et en extrusion. Les mélanges et films obtenus sont caractérisés par analyse en rhéologie dynamique, analyse thermique et analyse mécanique. Une dégradation de la matrice ainsi qu’une orientation des whiskers sont observées. Pour contourner ces contraintes, plusieurs alternatives sont utilisées. La première consiste à adsorber un copolymère sur les whiskers ; cette méthode augmente l’effet hydrodynamique mais aucun réseau n’est obtenu. La deuxième alternative est l’utilisation d’un polymère de faible masse molaire, permettant de diminuer la viscosité du mélange et par conséquent de limiter l’orientation des charges. Cette voie permet la formation d’un réseau percolant, tout en évitant la dégradation de la matrice dans l’extrudeuse. La troisième alternative utilise un copolymère de faible masse molaire synthétisé à partir d’un monomère porteur de doubles liaisons. La faible masse molaire permet de diminuer la cristallinité du séparateur et donc d’améliorer les performances ioniques à basse température. Les doubles liaisons permettent une réticulation assurant la tenue mécanique du film / The aim of this study is to produce high-performance battery separators through extrusion. These solid polymer electrolytes should be permeable to ionic current but electrically insulating, all the while maintaining sufficient mechanical resistance. To this end, the dispersion of nanometrics fillers (cellulose whiskers) in a polymer is studied. Cellulose whiskers are crystalline sticks, with a length between 100 and 300 nm and a diameter between 5 and 20 nm. It is well known that a homogeneous dispersion of these fillers allows a percolating network, improving the mechanical reinforcement of the matrix at low concentrations. The goal is to carry out this dispersion in molten polymer through extrusion, as opposed to the well-established solvent evaporation process. The main difficulties are the aggregation of cellulose whiskers which occurs through hydrogen bonding and the concentrated medium in which these fillers are dispersed. The first part of the study is to determine the optimum process to prepare cellulose whiskers in order to limit aggregation and thus obtain a stable aqueous suspension. This stable system is necessary to obtain a percolating network in the polymer matrix through solvent evaporation. Once the protocol optimised, the second part of the study focuses on the dispersion of these whiskers in the molten matrix using both the internal mixer and the extruder. Blends and films are characterized by dynamical rheology analysis, thermal analysis and mechanical analysis: a degradation of the matrix and an orientation of the whiskers are observed. To by-pass these issues, several alternatives are used. The first one involves the adsorption of a copolymer on the whiskers. This method increases the hydrodynamic effect; however no percolation network is obtained. The second alternative is to use a low molar mass polymer. This leads to a decreased polymer viscosity which limits the orientation of the fillers, allowing the percolating network to form and prevents polymer degradation. The third way uses a copolymer with a low mass molar, synthesized from a monomer which carries double bonds. The low molar mass allows the decrease of the separator crystallinity thus improving the ionic performances at low temperatures. The double bonds can crosslink under UV light, which enhances the mechanical strength of the film