Submitted by Ronildo Prado (ronisp@ufscar.br) on 2017-08-23T14:10:16Z No. of bitstreams: 1 DissPICC.pdf: 9243099 bytes, checksum: d5c4984be722eda91236fbec51d566f6 (MD5) / Approved for entry into archive by Ronildo Prado (ronisp@ufscar.br) on 2017-08-23T14:10:24Z (GMT) No. of bitstreams: 1 DissPICC.pdf: 9243099 bytes, checksum: d5c4984be722eda91236fbec51d566f6 (MD5) / Approved for entry into archive by Ronildo Prado (ronisp@ufscar.br) on 2017-08-23T14:10:29Z (GMT) No. of bitstreams: 1 DissPICC.pdf: 9243099 bytes, checksum: d5c4984be722eda91236fbec51d566f6 (MD5) / Made available in DSpace on 2017-08-23T14:10:35Z (GMT). No. of bitstreams: 1 DissPICC.pdf: 9243099 bytes, checksum: d5c4984be722eda91236fbec51d566f6 (MD5) Previous issue date: 2017-02-24 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / New materials from cellulose have been developed, such as cellulose nanocrystals (CNC) and cellulose nanofibrils (CNF). Different morphologies of the cellulose can lead to the formation of films with different thermal, mechanical and optical properties in relation to conventional cellulose films. The objective of this work was to evaluate the effect of different dimensional scales of cellulose, micro and nanometric, on the production of cellulose films from two vegetable species and their thermal, mechanical, morphological and optical properties. Eucalyptus fibers and pineapple leave fiber (curauá) (PALF) were used as cellulosic fibers for this study. The films of eucalyptus and pineapple cellulosic fibers were prepared by filtration and casting, and the CNC and CNF films were obtained by continuous casting. The CNC and CNF films showed mechanical tensile strength in the order of 9 to 35 MPa higher than the films of cellulose fibers, regardless of the origin of the fiber. The continuous casting process produced CNC and CNF films that presented different mechanical resistance in the longitudinal direction of the process with respect to the transverse direction. This behavior may be related to how hydrogen bonds and mechanical anchorages occur between nanofibers. The thermal stability of the nanocellulose films was lower in the order of 20 to 150 ºC than in the films of fibers due to the routes of obtaining the CNC and CNF. Nanofiber films presented lower opacity in the order of 3 to 60% lower than the films of fibers due to the diameter of the nanocelluloses. Curauá fibers had the highest crystallinity index (Ic) reaching 87%. It is concluded that the properties studied were influenced by the type of nanocellulose (CNC or CNF), the origin of the cellulose (eucalyptus or pineapple), and the micro and nanometric scale of the fibers. / Novos materiais a partir da celulose tem sido obtidos, como os nanocristais de celulose (CNC) e as nanofibrilas de celulose (CNF). Diferentes morfologias da celulose podem levar a formação de filmes com propriedades térmicas, mecânicas e ópticas diferentes de filmes de celulose convencional. O objetivo deste trabalho foi avaliar o efeito de diferentes morfologias de fibras de celulose, micro e nanométricas, na obtenção de filmes - provenientes de duas espécies vegetais – e em suas propriedades térmicas, mecânicas, ópticas e morfológicas. Utilizou-se como fibras celulósicas para este estudo as fibras de eucalipto e fibras de folhas de abacaxi (curauá) (PALF). Os filmes de fibras celulósicas de eucalipto e de abacaxi foram confeccionados por filtragem e casting, e os filmes de CNC e CNF foram obtidos por continuous casting. Os filmes de CNC e CNF apresentaram resistência mecânica à tração, na ordem de 9 a 35 MPa superior aos filmes de fibras de celulose, independente da origem da fibra. O processamento por continuous casting produziu filmes de CNC e CNF que apresentaram resistência mecânica diferente no sentido longitudinal ao processo com relação ao sentido transversal. Este comportamento pode estar relacionado de que forma ocorrem às ligações de hidrogênio e os emaranhamentos mecânicos entre as nanofibras. A estabilidade térmica dos filmes de nanofibra foi menor na ordem de 20 a 150 ºC do que aos filmes de fibras devido às rotas de obtenção das CNC e CNF. Os filmes de nanofibra apresentaram menor opacidade, na ordem de 3 a 60% inferior, que os filmes de fibras devido ao diâmetro das nanofibras. As fibras de curauá apresentaram o maior índice cristalinidade (Ic) chegando a 87%. Conclui-se que a propriedades estudadas foram influenciadas pelo tipo de nanofibra (CNC ou CNF), pela origem da celulose (eucalipto ou abacaxi), e pela escala micro e nanométrica das fibras.

L’originalité de ce travail est d’étudier la contribution des nanocelluloses pour limiter deux défauts courant dans les papiers sécurités: le froissage et les “cornes”, où plis qui se manifestent dans les angles des papiers. Ces défauts sont principalement causés par une manipulation quotidienne de ces papiers à haute valeur ajoutée, et sont responsables d’une perte en qualité visuelle et mécanique ainsi que de troubles économiques. Les nanocellulose peuvent être divisées en deux différentes familles de matériaux : les nanofibrilles de celluloses (NFCs) et les nanocristaux de cellulose (NCCs). Les NFCs sont longues et flexibles et peuvent facilement s’enchevêtrer pour former un réseau cohésif maintenu par de nombreuses liaisons hydrogènes. Les NCCs sont des matériaux petits et rigides, et leurs impressionantes propriétés mécaniques font d’eux des candidats intéressants pour être utilisés en renfort de polymère. Dans cette étude, deux stratégies sont proposées pour incorporer ces deux types de nanocellulose dans la fabrication du papier sécurité. Premièrement, il est question d’introduire une couche de NFCs à l’intérieur du papier afin d’augmenter la résistance de ce papier au froissage. Ensuite, il est question d’imprégner ce papier avec de l’alcool polyvinylique renforcé par des NCCs afin d’augmenter la résistance aux cornes. Enfin, ces approches sont testées à l’échelle pilote et industrielle. / The original feature of this work is the use of nanocellulose for limiting two security paper defects: corner folds, also called “dog-ears”, and crumpling. These defects, caused principally by daily handling of these high added value documents, are responsible for a decrease of paper visual and mechanical quality and constitute an economic loss. Nanocellulose can be divided into two different families: cellulose nanofibrils (CNFs) and cellulose nanocrystals (CNCs). CNFs are long and flexible materials with the ability to entangle and form a network strongly maintained by hydrogen bonds. CNCs are short and rigid materials whose outstanding mechanical properties make them good candidates for reinforcement in a polymer matrix. In this study, two strategies are proposed to incorporate these two kinds of nanocellulose in the security paper process. First, it is question to introduce a CNF layer within the paper substrate in order to increase the paper crumpling resistance. Then, it is question to impregnate the paper with CNCs-reinforced polyvinyl alcohol (PVOH) in order to increase the dog-ears resistance. Finally, these approaches are tested at pilot and industrial scales.

Submitted by Milena Rubi ( ri.bso@ufscar.br) on 2017-10-17T16:37:26Z No. of bitstreams: 1 SILVA_Barbara_2017.pdf: 2018251 bytes, checksum: 6dab58bc6d22c81d23f1cfb7011353bf (MD5) / Approved for entry into archive by Milena Rubi ( ri.bso@ufscar.br) on 2017-10-17T16:37:37Z (GMT) No. of bitstreams: 1 SILVA_Barbara_2017.pdf: 2018251 bytes, checksum: 6dab58bc6d22c81d23f1cfb7011353bf (MD5) / Approved for entry into archive by Milena Rubi ( ri.bso@ufscar.br) on 2017-10-17T16:37:47Z (GMT) No. of bitstreams: 1 SILVA_Barbara_2017.pdf: 2018251 bytes, checksum: 6dab58bc6d22c81d23f1cfb7011353bf (MD5) / Made available in DSpace on 2017-10-17T16:38:00Z (GMT). No. of bitstreams: 1 SILVA_Barbara_2017.pdf: 2018251 bytes, checksum: 6dab58bc6d22c81d23f1cfb7011353bf (MD5) Previous issue date: 2017-03-15 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / The application of cellulose nanofibrils to the production of composites has been studied and presents promising results, mainly due to the abundance of the material, which is of a renewable source, and to its low cost. However, the presence of the hydroxyl groups in their chain and their storage in aqueous solutions limits their application as reinforcement in nonpolar matrix composites. In this context, this work aimed to modify the wettability and adhesion properties of films of cellulose nanofibrils to apolar matrices, through plasma treatment. For this, nanocellulose films with thickness of 38 ? 8 ?m were produced by the casting method, from a suspension of nanofibrils in water. The atomic force microscopy characterization (AFM) of the suspended nanofibrils indicated that most of them have an average diameter of less than 75 nm. Each film obtained, after drying the suspension, was then cut into 13 samples with 2 x 1 cm, 12 of which were exposed to plasma and one stored as untreated. Three films were treated with oxygen plasma, with excitation power of 150 W, for 30 minutes and pressure of 0.1, 0.3 and 0.5 Torr. Another three films were treated with sulfur hexafluoride plasma at pressures of 0.1, 0.2 and 0.3 Torr, with a power of 150 W for 15 minutes. It was observed that weight loss was greater than 40% for the films treated with the most extreme conditions oxygen and sulfur hexafluoride. The results also showed that the treatments with sulfur hexafluoride promoted the reduction of the receptivity of the samples to the liquids, with contact angles of approximately 60º for water and 50º for diiodomethane. The profilometry technique revealed that the roughness of the films varied after the treatment with oxygen and sulfur hexafluoride, but the high error bars impede a definitive conclusion on the tendency of these variations. The X-ray diffraction analysis (XRD) indicated no significant change in the crystallinity of the samples with the treatments. In the Fourier Transform Infrared absorption spectra (FTIR), a C-F bonding related peak appeared for the 0.3 Torr sulfur hexafluoride treated sample, indicating the presence of fluorine in that sample. The scanning electron microscopy (SEM) allowed the visualization of the changes in the topography of the films, due to the etching processes resulting from the action of the plasma and the films ruptures caused by the high removal of surface material. In order to test the incorporation of treated films into composites using polyolefins as the matrix, polyethylene pellets were solubilized in xylene for the production of composite films. The treated and untreated nanocellulose films were placed in Petri dish jointly to the polyethylene films still dissolved and left at room temperature. After drying, adhesion between the films was tested through the adhesive tape test, resulting in class-zero adherence, according to the technical standard. It is believed that the lack of adhesion is a result of the composite production method that should be optimized for future work, in order to provide a better investigation of the effects of plasma on the surface properties of the film of cellulose nanofibrils. / A aplicação de nanofibrilas de celulose à produção de compósitos vem sendo estudada e apresenta resultados promissores, principalmente devido à abundância do material, que é de fonte renovável, e ao seu baixo custo. Contudo, a presença dos grupos hidroxila em sua cadeia e o seu armazenamento em soluções aquosas impede sua aplicação como reforço em compósitos de matrizes apolares. Nesse contexto, esse trabalho buscou modificar as propriedades de molhabilidade e aderência de filmes de nanofibrilas de celulose a matrizes apolares, através de tratamento a plasma. Para isso, filmes de nanocelulose com espessura de 38 ? 8 ?m foram produzidos pelo método de casting, a partir de uma suspensão de nanofibrilas em água. A caracterização por microscopia de força atômica (AFM) das nanofibrilas em suspensão indicou que a maior parte destas apresenta diâmetro médio inferior a 75 nm. Cada filme obtido, após a secagem da suspensão, foi então cortado em 13 amostras de 2 x 1 cm, sendo 12 destas expostas ao plasma e uma armazenada como não tratada. Três filmes foram tratados com plasma de oxigênio, com potência de excitação de 150 W, por 30 minutos e pressão de 0,1, 0,3 e 0,5 Torr. Outros três filmes foram tratados com plasma de hexafluoreto de enxofre, nas pressões 0,1, 0,2 e 0,3 Torr, com potência de 150 W por 15 minutos. Observou-se que houve perda de massa superior a 40% para os filmes tratados com as condições mais extremas de oxigênio e hexafluoreto de enxofre. Os resultados demonstraram também que os tratamentos com hexafluoreto de enxofre promoveram a diminuição da receptividade a líquidos das amostras, com ângulos de contato de aproximadamente 60º para água e 50º para o diiodometano. A técnica de perfilometria revelou que a rugosidade dos filmes variou após o tratamento com oxigênio e hexafluoreto de enxofre, porém as elevadas barras de erro impediram uma conclusão definitiva sobre a tendência dessas variações. As análises de difração de raios X (DRX) indicaram não haver alteração significativa na cristalinidade das amostras com os tratamentos. Nos espectros de absorção no infravermelho por transformada de Fourier (FTIR), foi observado o surgimento de um pico relacionado à ligação C-F para a amostra tratada com 0,3 Torr de hexafluoreto de enxofre, que indica a presença de flúor nessa amostra. As análises de microscopia eletrônica de varredura (MEV) permitiram visualizar as alterações na topografia dos filmes, devido aos processos de ecthing decorrentes da ação do plasma e os rompimentos ocasionados pela elevada remoção de material da superfície. A fim de testar a incorporação dos filmes tratados em compósitos que utilizam poliolefinas como matriz, pellets de polietileno foram solubilizados em xileno para produção de filmes compósitos. Os filmes de nanocelulose tratados e não tratados foram dispostos em placa de Petri junto aos filmes de polietileno ainda dissolvidos e deixados em temperatura ambiente. Depois de secos, a adesão entre os filmes foi testada através do teste de fita-cola, resultado em adesão classe zero, conforme a norma técnica. Acredita-se que a falta de adesão é resultado do método de produção do compósito que deve ser otimizado para trabalhos futuros, com o objetivo de proporcionar uma melhor investigação dos efeitos do plasma sobre as propriedades da superfície do filme de nanofibrilas de celulose.

<div> <p><a>Polymer nanocomposites are envisioned for use in many advanced applications, such as structural industries, aerospace, automotive technology and electronic materials, due to the improved properties like mechanical strengthening, thermal and chemical stability, easy bulk processing, and/or light-weight instigated by the filler-matrix combination compared to the neat matrix. In recent years, due to increasing environmental concerns, many industries are inclining towards developing sustainable and renewable polymer nanocomposites. Cellulose nanomaterials (CNs), including cellulose nanocrystals (CNCs) and cellulose nanofibrils (CNFs), have gained popularity due to their excellent mechanical properties and eco-friendliness (extracted from trees, algae, plants etc.). However, to develop CN-reinforced nanocomposites with industrial applications it is necessary to understand impact of hygroscopic swelling (which has very limited </a>quantitative study at present), aspect ratio, orientation, and content of CNs on the overall performance of nanocomposites; and overcome the low dispersibility of CNs and improve their compatibility with hydrophobic matrix. In this work, we attempt to understand the influence of single nanocrystals in the hygroscopic and optical response exhibited by nanostructured films; effect of CNCs on the properties of PVA/CNC fibers by experimental evidence with mathematical modeling predictions; and hydrophobized CNFs using a facile, aqueous surface modification to improve interfacial compatibility with epoxy. </p><p><br></p> <p>To evaluate the effect of CNC alignment in the bulk response to hygroscopic expansion, self-organized and shear-oriented CNC films were prepared under two different mechanisms. The coefficient of hygroscopic swelling (CHS) of these films was determined by using a new contact-free method of Contrast Enhanced Microscopy Digital Image Correlation (CEMDIC) that enabled the characterization of dimensional changes induced by hygroscopic swelling of the films. This method can be readily used for other soft materials to accurately measure hygroscopic strain in a non-destructive way. By calculating the CHS values of CNC films, it was determined that hygroscopic swelling is highly dependent on the alignment of nanocrystals within the films, with aligned CNC films showing dramatically reduced hygroscopic expansion than randomly oriented films. Finite element analysis was used to simulate moisture sorption and kinetics profile which further predicted moisture diffusion as the predominant mechanism for swelling of CNC films. </p> <p><br></p><p>To study the effects of different types and aspect ratios of CNCs on mechanical, thermal and morphological properties of polyvinyl alcohol (PVA) composite <a>fibers, CNCs extracted from wood pulp and cotton were reinforced into PVA to produce fibers by dry-jet-wet spinning. The fibers were collected as-spun and with first stage drawing up to draw ratio 2. </a>The elastic modulus and tensile strength of the fibers improved with increasing CNC content (5 – 15 wt. %) at the expense of their strain-to-failure. The mechanical properties of fibers with cotton CNC were higher than the fibers with wood CNC when the same amount of CNCs were added due to their higher aspect ratio. The degree of orientation along the spun fiber axis was quantified by 2D X-ray diffraction. As expected, the CNC orientation correlates to the mechanical properties of the composite fibers. Micromechanical models were used to predict the fiber performance and compare with experimental results. Finally, surface and cross-sectional morphologies of fibers were analyzed by scanning electron microscopy and optical microscopy.</p><p><br></p> <p>To improve the dispersibility and compatibility of CNFs with epoxy, CNFs were modified by using a two-step water-based method where tannic acid (TA) acts as a primer with CNF suspension and reacts with hexadecylamine (HDA), forming the modified product as CNF-TA-HDA. The modified (-m) and unmodified (-um) CNFs were filled into hydrophobic epoxy resin with a co-solvent (acetone), which was subsequently removed to form a solvent-free two component epoxy system, followed by addition of hardener to cure the resin. Better dispersion and stronger adhesion between fillers and epoxy were obtained for m-CNF than the um-CNF, resulting in better mechanical properties of nanocomposites at the same loading. Thermal stability and the degradation temperature of m-CNF/epoxy improved when compared to neat epoxy. </p> </div> <br>

Cellulose nanofibrils (CNFs) are nanoscale fibers of high aspect ratio that can be isolated from a wide variety of cellulosic sources, including wood and bacterial cellulose. With high strength despite of their low density, CNFs are a promising renewable building block for the preparation of nanostructured materials and composites. To fabricate CNF-based materials with improved inherent rheological and mechanical properties and additional new functionalities, it is essential to tailor the surface properties of individual CNFs. The surface structures control the interactions between CNFs and ultimately dictate the structure and macroscale properties of the bulk material. In this thesis we have demonstrated different approaches, ranging from non-covalent adsorption and covalent chemical modification to modification of cellulose biosynthesis, to tailor the structure and surface functionalities of CNFs for the fabrication of advanced materials. These materials possess enhanced properties such as water-redispersibility, water absorbency, dye adsorption capacity, antibacterial activity, and mechanical properties. In Paper I, CNFs were modified via the irreversible adsorption of carboxymethyl cellulose (CMC). The adsorption of small amounts of CMC onto the surface of CNFs prevented agglomeration and co-crystallization of the nanofibrils upon drying, and allowed the recovery of rheological and mechanical properties after redispersion of dried CNF samples. In Paper II, CNFs bearing permanent cationic charges were prepared through quaternization of wood pulp fibers followed by mechanical disintegration. The activation of the hydroxyl groups on pulp fibers by alkaline treatment was optimized prior to quaternization. This optimization resulted in individual CNFs with uniform width and tunable cationic charge densities. These cationic CNFs demonstrated ultrahigh water absorbency and high adsorption capacity for anionic dyes. In Paper III, via a similar approach as in Paper II, CNFs bearing polyethylene glycol (PEG) were prepared by covalently grafting PEG to carboxylated pulp fibers prior to mechanical disintegration. CNFs with a high surface chain density of PEG and a uniform width were oriented to produce macroscopic ribbons simply by mechanical stretching of the CNF hydrogel network before drying. The uniform grafted thin monolayer of PEG on the surface of individual CNFs prevented the agglomeration of CNFs and facilitated their alignment upon mechanical stretching, thus resulted in ribbons with ultrahigh tensile strength and modulus. These optically transparent ribbons also demonstrated interesting biaxial light scattering behavior. In Paper IV, bacterial cellulose (BC) was modified by the addition of chitin nanocrystals (ChNCs) into the growing culture medium of the bacteria Acetobacter aceti which secretes cellulose in the form of entangled nanofibers. This led to the in situ incorporation of ChNCs into the BC nanofibers network and resulted in BC/ChNC nanocomposites exhibiting bactericidal activity. Further, blending of BC nanofibers with ChNCs produced nanocomposite films with relatively lower tensile strength and modulus compared to the in situ cultivated ones. The bactericidal activity increased significantly with increasing amount of ChNCs for nanocomposites prepared by direct mixing of BC nanofibers and ChNCs. In Paper V, CNFs were isolated from suspension-cultured wild-type (WT) and cellulose-binding module (CBM) transformed tobacco BY-2 (Nicotiana tabacum L. cv bright yellow) cells. Results from strong sulfuric acid hydrolysis indicated that CNFs from transgenic cells overexpressing CBM consisted of longer cellulose nanocrystals compared to CNFs from WT cells. Nanopapers prepared from CNFs of transgenic cells demonstrated significantly enhanced toughness compared to CNFs of WT cells. / <p>QC 20141103</p> / CARBOMAT

Ce travail porte sur l'incorporation de nanorenforts biosourcés, c'est-à-dire des nanofibrilles de cellulose (NFC), dans les matériaux composites à matrice polymère et les mousses. Ces nouveaux matériaux biosourcés peuvent par exemple être utilisés pour la conception de structures sandwich. L'étude à caractère expérimental, théorique et numérique s'articule autour de trois axes visant à optimiser tant les procédés d'élaboration que les propriétés en service de ces matériaux.Dans un premier temps, la rhéologie des suspensions concentrées de NFC, fluides à seuil thixotropes, a été étudiée aux échelles macro- et mésoscopiques en utilisant un dispositif original de rhéométrie couplé à des mesures de champs cinématiques par vélocimétrie ultra-sonore. Nous montrons ainsi que l'écoulement des suspensions de NFC est fortement hétéro-gène et présente des glissements aux parois, de multiples bandes de cisaillement couplés avec des écoulements de type « bouchon ». Sur la base de cette étude, un modèle rhéolo-gique multi-échelles est proposé. Ce modèle tient compte d'une part de l'architecture aniso-trope des réseaux connectés de NFC dans ces suspensions, et d'autre part des interactions mécaniques et physico-chimiques aux échelles nanométriques. Il permet de montrer que les interactions colloïdales et hydrodynamiques, ainsi que la tortuosité et l'orientation des NFC jouent un rôle majeur sur la contrainte seuil et sur le comportement rhéofluidifiant de ces suspensions.Dans un deuxième temps, des nanocomposites à matrice polymère ont été élaborés sous forme de films en faisant varier sur une très grande plage la fraction volumique de NFC. En utilisant d'une part des techniques de microscopie (AFM, MEB) et de diffraction aux rayons X, et d'autre part des essais mécaniques (traction, DMA) nous montrons (i) que les NFC ont une orientation plane et s'organisent en réseaux connectés par des liaisons hydro-gènes, (ii) que ces réseaux jouent un rôle majeur sur le comportement mécanique des nano-composites et (iii) que le comportement élastique des nanocomposites est bien en deçà des prévisions données par les modèles micromécaniques de la littérature. De là, nous proposons un modèle multi-échelles alternatif où les principaux nano-mécanismes de déformation sont ceux se produisant dans les parties amorphes des NFC et au niveau des très nombreuses interfaces entre NFC.Enfin, nous avons étudié l'influence des conditions d'élaboration, de la nature et de la con-centration des NFC sur les microstructures (microtomographie synchrotron à rayons X), les propriétés mécaniques (essais de compression) et les micro-mécanismes de déformation (essai in situ en microtomographie) de mousses préparées par cryodessiccation de suspensions aqueuses de NFC. / This study focuses on the use of cellulose nanofibrils (NFCs) as bio-based nano-reinforcement in polymer composites and foams. These renewable materials can be used in place of traditional materials such as for instance to produce sandwich panels. This experi-mental, theoretical and numerical work aims at optimizing the processing of these NFC-based materials as well as their use properties.In the first part of this work, the rheology of concentrated NFC suspensions, that behave as thixotropic yield stress fluids, is investigated at macro- and mesoscales using an original rheo-ultrasonic velocimetry (rheo-USV) setup allowing the local flow kinematic to be obtai-ned. We show that the flow of NFC suspensions is highly heterogeneous and exhibits com-plex situations with the coexistence of wall slippage, multiple shear bands and plug-like flow bands. Using this experimental database, we develop an original multiscale rheological model for the prediction of the rheology of NFC suspensions. The model takes into account the anisotropic fibrous nature of NFC networks as well as colloidal and mechanical interaction forces occurring at the nanoscale. The model predictions prove that colloidal and hydrody-namic interaction forces together with the orientation and the wavy nature of NFCs play a major role on the yield stress and shear thinning behaviour of the suspensions.In the second part of this work, NFC-reinforced polymer nanocomposite films are processed for a wide range of NFC contents. Using advanced microscopy techniques (AFM, SEM), X-ray diffraction and mechanical tests (tensile and DMA tests), we show (i) that NFCs form highly connected nanofibrous structures with in-plane random orientation, (ii) that these connected NFC networks play a leading role on the mechanical behaviour of the nanocompo-sites and (iii) that the elastic properties of nanocomposite films are much lower than those predicted from the micromechanical models of the literature. In light of these observations, we propose an alternative multiscale model in which the main involved deformation nano-mechanisms are those occurring both in the amorphous segments of the nanofibers and in the numerous nanofiber-nanofiber contact zones.Finally, in a third part we focus on the influence of the processing conditions, the suspension type and the NFC concentration on the microstructure (using X-ray synchrotron microto-mography), the mechanical properties (using compression tests) and the deformation micro-mechanisms (using in situ compression test with X-ray microtomography) of various foams prepared from NFC suspensions by freeze-drying.

Cellulose nanofibrils (CNF) is a renewable material with unique strength properties. A difficulty in CNF production is that CNF suspensions contain large amounts of water. If CNF suspension volume can be decreased by dewatering facilitated by centrifugation, then transportation costs and storage costs can be reduced. The aim of this thesis is to investigate the impact various parameters have on CNF centrifugation dewatering and identify optimal conditions for maximal water removal. A laboratory study was conducted using four materials; 2.0 w% enzymatically treated CNF (CNF1), 1.9 w% carboxymethylated CNF (CNF2) and two commercial samples (1.9 w% CNFA and 1.8 w% CNFB). The main method was analytical centrifugation up to 2330 g. Parameters tested were initial concentration before centrifugation, temperature, NaCl addition, pH, and applied solid compressive pressure (g-force and surface weight). In addition to centrifugation experiments the four materials were characterized with laser diffraction, UV-vis absorption, Dynamic light scattering, and dry weight measurements. Analysis of the experimental data collected show that increase in initial concentration give a higher final concentration, but less water is removed. Furthermore, temperature changes have no effect on separation of CNF and water. At an applied solid compressive pressure of 3 kPa and initial concentration at 1.5 w% the concentrations 5.5 w%, 1.5 w%, 4.0 w%, and 4.3 w% can be reach for CNF1, CNF2, CNFA, and CNFB respectively. After extrapolation of polynomial functions fitted to experimental data an applied solid compressive pressure of 22 kPa and initial concentration at 1:5 w%, the concentrations 9.1 w%, 1.5 w%, 6.9 w%, and 7.9 w% are predicted for CNF1, CNF2, CNFA, and CNFB respectively. The thickening of CNF suspensions achieved and predicted in this thesis implies possibilities for large amounts of water removal, e.g. the water content in a CNF1 suspension is reduced from 65.7 litres/kg CNF to 10.0 litres/kg CNF at the solid compressive pressure 22 kPa. The concentrations at 22 kPa are determined by extrapolation from experimental data &lt;3 kPa solid compressive pressure. The carboxymethylated CNF2 can not be dewatered unless it is diluted or if salt or pH is adjusted. This is directly correlated to the electrostatic forces in the suspension and the Debye length. Addition of salt or lowered pH also eliminate any concentration gradients in diluted and centrifuged CNF2 suspensions. / Cellulosa nanofibriller (CNF) är ett förnybart material med unika styrkeegenskaper. En svårighet med produktion av CNF är att CNF suspensioner innehåller stora mängder vatten. Om volymerna av CNF suspensioner kan minskas med avvattning genom centrifugering, då kan transport- och lagerkostnader sänkas. Målet med det här examensarbetet är att undersöka vilken inverkan olika parametrar har på CNF-avvattning genom centrifugering och identifiera optimala förhållanden för maximalt avlägsnande av vatten. En laboratoriestudie utfördes på fyra olika material. De fyra materialen är 2 w% enzymatiskt behandlad CNF (CNF1), 1.9 w% karboxymetylerad CNF (CNF2) och två kommersiella prover (1.9 w% CNFA och 1.8 w% CNFB). Den huvudsakliga metoden var analytisk centrifugering upp till maximalt 2330 g. De testade parametrarna var initial koncentration innan centrifugering, temperatur, NaCl tillsats, pH, och applicerat fast kompressionstryck (g-kraft och ytvikt). Förutom centrifugeringsexperimenten så karaktäriserades the fyra mmaterialen med laser diffraktion, UV-vis absorption, dynamisk ljusspridning och vägningar av torrhalt. Analys av den experimentella data som insamlats visar att en ökad initial koncentration ger en högre slutkoncnentration, men mindre vatten kan bortföras. Temperaturförändringar har ingen effekt på separation av CNF och vatten. Vid ett applicerat fast kompressibelt tryck på 3 kPa och en initial koncentration 1.5 w% kan koncentrationerna 5.5 w%, 1.5 w%, 4.0 w%, och 4.3 w% nås för CNF1, CNF2, CNFA, och CNFB. Efter extrapolering av polynoma funktioner passad till experimentell data förutspås att koncentrationerna 9.1 w%, 1.5 w%, 6.9 w%, och 7.9 w% kan nås för CNF1, CNF2, CNFA, and CNFB vid 22 kPa och en initial koncentration på 1.5 w%. Förtjockningen av CNF suspensioner som kan, eller förutspås kunna nås genom centrifugering i det här examensarbetet innebär att det är möjligt att avlägsna stora mängder vatten, till exempel kan vatteninnehållet i CNF1 minskas från 65.7 liter/kg CNF till 10.0 liter/kg CNF vid 22 kPa fast kompressionstryck. Koncentrationerna vid 22 kPa fast kompressionstryck är extrapolerade från exprimentell data &lt;3 kPa fast kompressionstryck. Den karboy- metylerade CNF2 kan inte avvattnas om den inte späds ut eller om salt eller pH justeras. Detta är direkt kopplat till de elektrostatiska krafterna i suspensionen och Debye längden. Tillsats av salt eller sänkt pH eliminerar också de koncentrationsgradienter som kan förekomma i utspädda centrifugerade CNF2 suspensioner.

Transparenta papper tillverkade av cellulosa nanofibriller (CNF), visar stor potential att kunna ersätta petroleumbaserade plaster inom många användningsområden, till exempel för mat- och varuförpackningar. CNF, även känt som nanocellulosa, kombinerar viktiga cellulosaegenskaper, med unika egenskaper hos nanomaterial. Denna kombination av egenskaper möjliggör tillverkning av ett pappers-liknande material som uppvisar både utmärkta mekaniska egenskaper och hög transparens. Användningen av nanocellulosa är dock förknippad med diverse utmaningar, för att materialet ska kunna bli kommersiellt slagkraftigt. En av de främsta utmaningarna är nanocellulosas höga affinitet för vatten och dess höga specifika yta som försvårar hanteringen av materialet. Avvattningen av nanocellulosadispersioner, för att tillverka transparenta papper, kan ta upp till flera timmar. För att övervinna detta hinder, har avdelningen för Fiberteknologi vid KTH tillsammans med BillerudKorsnäs AB, nyligen utvecklat en metodik för att skapa så kallade själv-fibrillerande fibrer (SFFer). Dessa fibrer möjliggör en snabbavvattnad papperstillverkningsprocess med makroskopiska vedbaserade fibrer, som efter tillverkning av pappret omvandlas till ett nanocellulosapapper, det vill säga ett nanopapper. För att erhålla SFFer krävs det att höga koncentrationer av karboxyl- och aldehydgrupper introduceras i cellulosafibrerna. Införandet av dessa funktionella grupper, möjliggör självfibrilleringen då SFFerna utsätts för moderata alkali-koncentrationer. I den ursprungliga studien som utfördes av Gorur m.fl., introducerades de funktionella grupperna med hjälp av sekventiell TEMPO- och periodatoxidation. I detta examensarbete, har alternativa kemiska metoder för att introducera samma kemiska funktionalitet som TEMPO-periodatsystemet undersökts. Huvudsyftet med arbetet är att besvara frågan: Hur påverkar olika kemiska behandlingar vid SFF tillverkningen, de kemiska och fysikaliska egenskaperna hos de modifierade fibrerna, samt de slutgiltiga pappersegenskaperna? För att besvara frågan, preparerades fibrer med liknande karboxyl- och aldehydinnehåll med hjälp av följande tre kemiska metoder: 1) TEMPO- följd av periodatoxidation (detta kommer att användas som referenssystem); 2) periodat- följd av kloritoxidation; 3) karboxymetylering följd av periodatoxidation. Egenskaperna hos fibrerna undersöktes med avseende på aldehyd- och karboxylinnehåll, avvattningspotential och förmåga att självfibrillera. Papper tillverkades med hjälp av en vakuumfiltreringsuppställning och följande egenskaper undersöktes hos pappret: mekaniska egenskaper (dragstyrka, brottsyrka och Young’s modul); optiska (transparens och ytreflektion); samt syrgaspermeabilitet. De erhållna fibrerna från samtliga tre kemiska modifieringar visade på självfibrillerande egenskaper i alkaliska lösningar. Detta beteende styrker hypotesen att ett strategiskt införande av ett högt karboxyl- och aldehydinnehåll leder till självfibrillerande fibrer. Transparenta papper tillverkade av fibrer som utsatts för TEMPO-periodatoxidation samt klorit-periodatoxidation, visade på utmärkta mekaniska egenskaper, hög transparens och bra barriäregenskaper - jämförbara med vad som vanligen kan noteras hos papper tillverkat av nanocellulosa. Samtliga egenskaper förbättrades ytterligare efter fibrillering av fibrerna i papperen. De karboxymetylerade-periodatoxiderade materialet, å andra sidan, uppvisade andra egenskaper jämfört med de två, tidigare nämnda, metoderna. TEMPO-periodat- och periodat-klorit-pappersmassan var halvgenomskinlig och geléliknande, medan den karboxymetylerade-periodatoxiderade massan var mer lik det omodifierade materialet. Detsamma gällde det tillverkade pappret som liknade ett konventionellt papper. Det var inte heller möjligt att åstadkomma en fibrillering av det karboxymetylerade-periodatoxiderade-pappret som utsattes för behandling med alkaliska lösningar. Avvattningstiden vid papperstillverkningen varierad mellan 4 och 60 sekunder, och karboxymetylering-periodat oxidation visade på snabbast avvattningstid. Den förlängda avvattningstiden i jämförelse med studien utförd av Gorur m.fl., tros främst bero på att ett filtreringsmembran med mindre porer användes på vakuumfiltreringsuppställningen, istället för en avvattningsvira som tidigare använts. Sammanfattningsvis så har det visat sig möjligt att tillverka självfibrillerande fibrer med hjälp av samtliga tre undersökta kemiska modifieringar. SFFer möjliggör tillverkning av snabbavvattnade transparenta nanocellulosapapper och visar på så vis på hög potential att kunna ersätta olje-baserade plaster till många förpackningsapplikationer. / Transparent papers made from cellulose nanofibrils (CNF), derived from e.g. wood, show great potential to replace petroleum-based plastics in many application areas, such as packaging for foods and goods. CNF, also known as nanocellulose, combine important cellulose properties with the unique features of nanoscale materials, gaining paper-like materials with outstanding mechanical properties and high transparency. However, nanocellulose faces various challenges in order to make the products commercially competitive. One of the main challenges is accompanied with nanocelluloses’ high affinity for water, which makes processing difficult. Dewatering of a nanocellulose dispersion in order to produce transparent paper may take up to several hours. To overcome this obstacle, the Fibre technology division at KTH Royal Institute of technology and BillerudKorsnäs AB have recently developed a new concept of self-fibrillating fibres (SFFs). This material enables fast-dewatering papermaking using fibres of native dimensions and conversion into nanocellulose after the paper has been prepared. In order to obtain SFFs, proper amounts of charged groups and aldehyde groups need to be introduced into the cellulose backbone. When SFFs are exposed to high alkali concentration, i.e. &gt; pH=10, the fibres self-fibrillates into CNFs. In the original study, the functional groups were introduced through sequential TEMPO oxidation and periodate oxidation. In this work, alternative chemical routes have been examined to prepare SFFs with the same functional groups as introduced with the TEMPO-periodate system. The aim of the thesis has been to answer: how does different chemical routes to prepare transparent nanopaper made from SFFs affect the chemical and physical properties of the modified fibres, as well as the final physical properties of the transparent papers? To answer the question, fibres with similar carboxyl and aldehyde contents were prepared using three chemical routes: 1) TEMPO oxidation followed by periodate oxidation (which was used as reference system); 2) periodate oxidation followed by chlorite oxidation; 3) carboxymethylation followed by periodate oxidation. The properties of the fibres were examined regarding aldehyde and carboxyl content, dewatering potential and self-fibrillating ability. Papers were produced using a vacuum filtration set-up and the properties investigated were the mechanical; tensile strength, strain at failure and Young’s modulus, the optical properties; transparency and haze, as well as the oxygen permeability. In order to investigate the impact of the fibrillation of the papers, the properties were measured for both unfibrillated and fibrillated samples. Furthermore, the gravimetric yield after each chemical modification procedure was examined, as well as the dewatering time during sheet making. Fibres obtained from all three chemistries demonstrated self-fibrillating properties in alkaline solutions. This strengthens the hypothesis that the strategical introduction of aldehydes and carboxyl groups is the main feature responsible for the self-fibrillating ability of the fibres. Transparent papers made from fibres treated through TEMPO-periodate oxidation and periodate-chlorite oxidation showed excellent mechanical, optical and barrier properties, comparable to those seen in nanocellulose papers. The properties were further increased after fibrillation. The carboxymethylated-periodate oxidized fibres, on the other hand, behaved differently from the others. While the TEMPO-periodate and periodate-chlorite pulp was semi-translucent and gel-like, the carboxymethylated-periodate oxidized fibres resembled more the unmodified material. Likewise, the properties of those papers resembled conventional paper and no fibrillationwas experienced after immersing the papers in alkaline solution, according to the same protocol developed for the other two chemistries. The dewatering time during sheet making ranged from 4–60 seconds (carboxymethylation-periodate oxidation showing the fastest dewatering rates). The increased dewatering time compared to earlier studies is believed to mainly be due to the use of a filtration membrane on the vacuum filtration set-up, instead of a metallic wire with larger pores. Overall, SFFs was successfully produced using three different chemical routes. SFFs enables production of fast-dewatering transparent nanocellulose papers that shows the potential to replace oil-based plastics in many packaging applications.

Abstract  Lack of clinical relevance is assumed to be the main reason behind the high failure rate of medical drugs in the very initial phases of clinical trials. Clinical relevance is difficult to achieve with current tools as they lack the biological and physiological cues found in vivo. Microfluidics, the knowledge of fluid manipulation in small channels, has proven to be a promising science to bridge the gap between the current in vitro and the real in vivo features. In this thesis, a scaffold for the growth of spheroids inside a microfluidic device for potential drug screening was developed. Firstly, the surface of a microfluidic device was coated with the polymers cellulose nanofibrils, polyallylamine hydrochloride, and polyethyleneimine using the Layer-by-Layer technique to achieve an even surface coverage. Here, different chip designs, polymer concentrations, and pressure directions were tested. It was decided that using a negative pressure direction with a polymer concentration of 50 mg/L in a chip design with micropillars was optimal and these conditions were then used for testing the spheroid formation. Secondly, spheroids were grown inside the microfluidic channels using different coatings: the previously mentioned polymer buildup, one non-coated channel, and one coated with attachment factor proteins. These three surface conditions were compared and it was shown that the polymer-based surface cover was indeed superior as a scaffold as it encouraged and promoted cell growth in the spheroid formation of liver cancer cells from the HepG2 cell line. Further development of this cellulose nanofibrils-coated microfluidic device displays a promising future for functioning as an in vitro 3D cell culture model that better mimics the close-to-cell microenvironments by imitating cell proliferation, cell-to-cell, and cell-to-extracellular matrix interactions. / Sammanfattning Den främsta orsaken bakom den höga antal misslyckade kliniska läkemedelsprövningar i de initiala faserna antas bero på brist på klinisk relevans. Klinisk relevans är mycket svår att uppnå med dagens verktyg då de saknar de biologiska och fysiologiska förhållandena som återfinns in vivo. Mikrofluidik, kunskapen om vätskemanipulation i små kanaler har visat sig vara lovande vetenskap för att överbrygga klyftan mellan de nuvarande in vitro och de faktiska in vivo funktionerna. I detta arbete utvecklades en matris för sfäroider att växa på inuti en mikrofluidisk kanal för att potentiellt användas till läkemedelsscreening. Först användes Layer-by-Layer teknologi för att jämnt betäckta ytan inuti en mikrofluidisk kanal med polymererna cellulosananofibriller, polyallylamin hydroklorid samt polyetylenimin. Här testades olika designer på mikrofluidiska chip, polymerkoncentrationer samt tryckriktningar. Utifrån detta gick det att fastställa att negativt tryck med en polymerkoncentration på 50 mg/L i en chippdesign med mikropelare var optimal för en jämn ytbetäckning och dessa förhållanden användes sedan för att pröva sfäroidernas tillväxt. Härnäst testades därmed sfäroidernas tillväxt inuti mikrofluidiska kanaler under tre olika förhållanden: ett med polymerbetäckningen, ett utan betäckning och ett då ytan var täckt med proteiner med fästfaktorer. Dessa tre förhållanden jämfördes sedan med varandra och således gick det att konstatera att den polymerbaseradebetäckningen fungerade överlägset som matris för tillväxt av HepG2 lever cancer cell sfäroider eftersom den tycks främja dess tillväxt och bildning. Det pekar mot att ytterligare utveckling av denna cellulostäckta yta skulle innebära en lovande modell för in vitro 3D cellodling som bättre efterliknar den cellulära mikromiljön genom att imitera cellproliferation, interaktioner celler emellan samt mellan cell och extracellulär matrisen.

Nanokompositfilmer med fem olika sammansättningar av hexagonala bornitrid nanosheet och TEMPO-CNF tillverkades med hjälp av vakuumassisterad filtreringsteknik. sond-ultraljudsteknik användes som en grön väg för exfoliering av bornitridpulver i vattenhaltigt medium. TEMPO-CNF spelade nyckelroller som både matris och dispergeringsmedel för stabilisering av bornitrid nanosheets i kompositen. Nanokompositfilmerna var flexibla och formbara och de visade höga mekaniska egenskaper inklusive hög draghållfasthet och god brottöjning. / Nanocomposite films with five different compositions of hexagonal boron nitride nanosheets and TEMPO-CNF were fabricated using vacuum-assisted filtration technique. probe-ultrasonication technique was applied as a green route for exfoliation of boron nitride powder in aqueous medium. TEMPO-CNF played key roles as both matrix and dispersant agent for stabilization of the boron nitride nanosheets in the composite. The nanocomposite films were flexible and ductile, and they showed high mechanical properties including high tensile strength and good elongation at break.