The exceptional properties of carbon nanomaterials make them ideal reinforcements for polymers. However, the main challenges in utilizing their unique properties are their tendency to form agglomerates, their non-controlled orientation, non-homogeneous distribution and finally the change in their shape/size due to processing. All the above are the result of the nanomaterial/polymer interfacial interactions which dictate the overall performance of the composites including the mechanical properties. The aforementioned uncertainties are the reason for the deviation observed between the experimentally determined properties and the theoretically expected ones. The focus of this study is to understand the reinforcing efficiency of carbon nanomaterials in polymers through finite element modeling that captures the effect of the interfacial interactions on the tensile modulus of polymer nanocomposites (PNCs). The novelty of this work is that the probability distribution functions of nanomaterials dispersion, distribution, orientation and waviness, determined through image analysis by extracting 3-D information from 2-D scanning electron micrographs, are incorporated into the finite element model allowing thus for fundamental understanding of how the nanostructure parameters affect the tensile modulus of the PNCs. The nanocomposites are made using melt mixing followed by either injections molding or melt spinning of fibers. Polypropylene (PP) is used as the polymer and carbon nanotubes (CNT) or exfoliated graphite nanoplatelets (xGnP) are used as nanoreinforcements. The presence of interphase, confirmed and characterized in terms of stiffness and width using atomic force microscopy, is also accounted for in the model. The dispersion and distribution of CNT within the polymer is experimentally altered by using a surfactant and by forcing the molten material to flow through a narrow orifice (melt spinning) that promotes alignment of CNT and even of the polymer chains along the flow/drawing direction. The effect of nanomaterials' geometry on the mechanical behavior of PNCs is also studied by comparing the properties of CNT/PP to those of xGnP/PP composites. Finally the reinforcing efficiency of CNT is determined independently of the viscoelastic behavior of the polymer by conducting tensile testing at temperatures below the glass transition temperature of PP. The finite element model with the incorporated image analysis subroutine has sufficient resolution to distinguish among the different cases (dispersion, distribution, geometry and alignment of nanomaterials) and the predicted tensile modulus is in agreement with the experimentally determined one. In conclusion, this study provides a tool, that integrates finite element modeling and thorough experiments that enables design of polymer nanocomposites with engineered mechanical properties.

One of the important dynamic parameter characterizing the properties of polymer nanocomposite is viscosity. It is a quantity of interest on macroscopic scale also. A thorough study of viscosity in case of polymer nanocomposite has not been carried out in the existing literature. In this work we used atomic force microscope, force-distance spectroscopy to experimentally measure the viscosity of polymer and polymer nanocomposite thin films. In particular we try to tune viscosity by changing the nature of interface of polymer grafted nanoparticle and polymer melt. The interface nature in varied by changing the miscibility parameter ( f ), defined as the ratio of grafted chain length to the matrix chain length. Using coarse-grained molecular dynamic simulations, dynamics at the nanoparticle-matrix interface is explored by calculating slip length and mobility at the interface. Equilibrium molecular dynamic simulation is employed to calculate the viscosity of nanocomposite. Chapter 1 We introduce some basic models for polymer chain conformation and dynamics. The known facts about the structural and dynamics of polymer grafted nanoparticle are also described. Chapter 2 We present our experiment method and results for various nanocomposite systems for two different volume fractions of nanoparticles and for two different thicknesses. We show that introduction of nanoparticles causes reduction in viscosity of thin film with respect to the neat polymer films. Further for the low volume fraction system (0:5%) the extent of reduction decreases with increasing f -value and almost matching the neat system at the highest f . At high volume fraction (1%), for lower f we observe a reduction in viscosity and for highest f surprisingly there is an increase in viscosity of nanocomposite with respect to the neat system with a cross-over for intermediate f . We attribute the effects to possible slip at the nanoparticle-matrix interface. A rough estimation of slip length from the measured value of viscosity of nanocomposite and pure polymer is provided which strongly supports our idea of slip at the interface Chapter 3 Briefly discusses some basic aspects of molecular dynamic simulation. Chapter 4 Using MD simulation we calculate the slip-length at the grafted nanoparticle-matrix interface for various systems with different f values. A spherical core grafted with atoms same as the matrix is kept fixed at the canter of simulation box. The particle is rotated for calculating slip length. We also look at the mobility variation of matrix chains as a function of radial distance from the centre of nanoparticle. From both slip-length and mobility calculation we observe that slip length as well as mobility is higher for lower f systems as compared to higher f thus supporting our assertion of slip as the most likely cause for our experimental observations. Chapter 5 Now instead of single grafted nanoparticle we have multiple nanoparticles which are free to move in the matrix. Using Green-Kubo formalism we calculate the equilibrium viscosity for pure polymer and nanocomposite systems from MD simulations. We observe increase in viscosity for nanocomposite system as compared to the pure polymer system. We also look at various structural and dynamical changes, that occurs in the filled system with respect to neat system, that leads to such increase in viscosity.

Orientador: Prof. Dr. Wendel Andrade Alves / Tese (doutorado) - Universidade Federal do ABC, Programa de Pós-Graduação em Nanociências e Materiais Avançados, 2017. / Os nanocompósitos baseados em biopolímeros mostram-se materiais promissores na construção de dispositivos para aplicações na área biomédica. Dentre estes, o poli(álcool vinílico) vem sendo amplamente empregado em sistemas de curativos inteligentes, uma vez que permite a incorporação de drogas e de proteínas preservando a atividade farmacológica. Neste trabalho, apresentamos a proposta de um material, preparado por eletrofiação, composto pelo poli(álcool viníco) (PVA) parcialmente hidrolisado (matriz polimérica) e de nanotubos de titanato de sódio (NTTi), que possui propriedades bactericidas (fase dispersa). O material foi avaliado à temperatura ambiente nas concentrações de 0% a 10% de NTTi. As propriedades morfológicas e estruturais dos nanocompósitos foram investigadas por diferentes técnicas analíticas, espectroscópicas e microscópicas. Os resultados obtidos mostraram que, os NTTi promoveram variações microestruturais na rede polimérica, impactando no diâmetro médio das fibras (~140-220 nm), na cristalinidade (43 - 50%) e na porosidade (68 - 58%). Como consequência, tais variações foram associadas ao comportamento viscoelástico da matriz. O aumento da concentração de NTTi contribuiu para uma redução nos valores dos módulos de armazenamento (~350 ¿ 220 MPa) e perda (~30 ¿ 25 MPa) o que indica uma melhora na propriedade de tenacidade. Os testes de permeação em células de Franz por 48 horas mostraram que, nos tipos de mantas de PVA (0% e com 5,0% NTTi) avaliadas o processo de permeação da albumina sérica bovina (BSA) se inicia a partir de seis horas de coleta e é mais regular na manta contendo 5,0% de NTTi. / Biopolymers based nanocomposites are promising materials for the construction of devices for biomedical applications. Among these, polyvinyl alcohol has been widely used in intelligent dressing systems, since it allows the incorporation of drugs and proteins preserving the pharmacological activity. In this work, we present the proposal of a material, prepared by electrospinning, composed of partially hydrolyzed polyvinyl alcohol (PVA) (polymer matrix) and sodium titanate nanotubes (NTTi), which has bactericidal (dispersed phase) properties. The electrospun fibrous mats was evaluated at room temperature at concentrations of 0% to 10% NTTi. The morphological and structural properties of the nanocomposites were investigated by analytical, spectroscopic and microscopic techniques. The results showed that the NTTi promoted microstructural variations in the polymer matrix, impacting the mean fiber diameter (~ 140-220 nm), the crystallinity (43 - 50%) and the porosity (68 - 58%). Consequently, such variations were associated with the viscoelastic behavior of the matrix. The increase in NTTi concentration contributed to a reduction in storage modulus values (~ 350 - 220 MPa) and loss (~ 30 - 25 MPa) indicating an improvement in tenacity property. Permeation tests on Franz cells for 48 hours showed that the permeation of bovine serum albumin (BSA) occurs in both PVA mats (0% and 5.0% NTTi), but it is easier the membrane only of PVA.

The barrier properties and long term strength retention of polymers are of significant importance in a number of applications. Enhanced lifetime food packaging, substrates for OLED based flexible displays and long duration scientific balloons are among them. Higher material requirements in these applications drive the need for an accurate measurement system. Therefore, a new system was engineered with enhanced sensitivity and accuracy. Permeability of polymers is affected by permeant solubility and diffusion. One effort to decrease diffusion rates is via increasing the transport path length. We explore this through dispersion of layered silicates into polymers. Layered silicates with effective aspect ratio of 1000:1 have shown promise in improving the barrier and mechanical properties of polymers. The surface of these inorganic silicates was modified with surfactants to improve the interaction with organic polymers. The micro and nanoscale dispersion of the layered silicates was probed using optical and transmission microscopy as well as x-ray diffraction. Thermal transitions were analyzed using differential scanning calorimetry. Mechanical and permeability measurements were correlated to the dispersion and increased density. The essential structure-property relationships were established by comparing semicrystalline and amorphous polymers. Semicrystalline polymers selected were nylon-6 and polyethylene terephthalate. The amorphous polymer was polyethylene terphthalate-glycol. Densification due to the layered silicate in both semicrystalline and amorphous polymers was associated with significant impact on barrier and long term creep behavior. The inferences were confirmed by investigating a semi-crystalline polymer - polyethylene - above and below the glass transition. The results show that the layered silicate influences the amorphous segments in polymers and barrier properties are affected by synergistic influences of densification and uniform dispersion of the layered silicates.

Tato dizertační práce je zaměřená na základní výzkum procesů samouspořádávání nanočástic v polymerních kapalinách a na vlastnosti připravených polymerních nanokompozitů s řízenou disperzí nanočástic. Navzdory současnému pokroku v porozumění polymerních nanokompozitech, stále chybí mnohé fundamentální znalosti relaxačních a mechanických vlastností polymerních nanostruktur, které by mohly poskytnout klíčové informace pro návrh hierarchických funkčních kompozitů zpracovatelných aditivními výrobními technikami. Hlavní důraz byl kladen na výzkum vlivu postupu přípravy nanokompozitu na finální stav disperze nanočástic, přípravu řízených nanostruktur – individuálně dispergované nanočástice, řetězci vázáné klastry a kontaktní agregáty - a určení jejich relaxačních a mechanických vlastností. Navíc byly nanočástice využity jako „sondy“ v polymerní matrici, které ovlivňují segmentální uspořádání a relaxační dynamiku polymerních řetězců a mohou poskytnout o těchto dějích zásadní informace. Tento přístup může pomoci nalezení vztahů mezi segmentální dynamikou na nano škále a mechanickými vlastnostmi polymerních skel na makro škále, což je náročný fundamentální problém s extrémní technologickou důležitostí. Neroubované keramické nanočástice a polymerní skla byly použity, aby se minimalizoval vliv silných interakcí mezi nanočásticemi a řetězci. Podrobný výzkum byl vykonán na modelovém systému PMMA/SiO2 a následně rozšířen na systémy s jinými matricemi (PC a PS) a jinými nanočásticemi (ZnO2 and Fe2O3) za účelem zobecnění obdržených výsledků. Byla určena závislost relaxačních a mechanických vlastností (teplota skelného přechodu, reptační čas, modul kaučukovitého plata, počet zapletenin, napětí na mezi kluzu, pokles napětí po mezi kluzu, elastický modul, modul deformačního zpevnění a odezvy při toku za studeny) na nanostruktuře, objemovém zlomku a složení. Získané výsledky byly interpretovány za použití současných modelů. Stanovené relaxační a mechanické vlastnosti byly propojeny, aby poskytli informace o molekulárních deformačních procesech řídících mechanickou odezvu makroskopických kompozitních těles.

No description available.

Polymer bonded explosives (PBXs) are composites comprised of energetic crystals with a very high energy density surrounded by a polymer binder. The formation of hotspots within polymer bonded explosives can lead to the thermal decomposition and initiation of the energetic material. A frictional heating model is applied at the mesoscale to assess the potential for the formation of hotspots under low velocity impact loadings. Monitoring of the formation and growth of damage at the mesoscale is considered through the inclusion of a piezoresistive carbon nanotube network within the energetic binder providing embedded strain and damage sensing. A coupled multiphysics thermo-electro-mechanical peridynamics framework is developed to perform computational simulations on an energetic material microstructure subject to these low velocity impact loads. With increase in impact energy, the model predicts larger amounts of sensing and damage thereby supporting the use of carbon nanotubes to assess damage growth and subsequent formation of hotspots. The framework is also applied to assess the combined effects of thermal loading due to prescribed hotspots with inertial effects due to low velocity impact loading. It has been found that the present model is able to detect the presence of hotspot dominated regions within the energetic material through the piezoresistive sensing mechanism. The influence of prescribed hotspots on the thermo-electro-mechanical response of the energetic material under a combination of thermal and inertial loading was observed to dominate the lower velocity impact response via thermal shock damage. In contrast, the higher velocity impact energies demonstrated an inertially dominated damage response. Quantifying the piezoresistive effect derived from embedding carbon nanotubes in polymers remains a challenge since these nanocomposites exhibit significant variation in their electro-mechanical properties depending upon factors such as CNT volume fraction, CNT dispersion, CNT alignment and properties of the polymer. Of interest is electrical percolation where the electrical conductivity of the CNT/polymer nanocomposite increases through orders of magnitude with increase in CNT volume fraction. Estimates and distributions for the electrical conductivity and piezoresistive coefficients of the CNT/polymer nanocomposite are obtained and analyzed with increasing CNT volume fraction and varying barrier potential, which is a parameter that controls the extent of electron tunneling. The effect of CNT alignment is analyzed by comparing the electro-mechanical properties in the alignment direction versus the transverse direction for different orientation conditions. Estimates of piezoresistive coefficients are converted into gage factors and compared with experimental sources in literature. The methodology for this work uses automated scripts which are used in conjunction with high performance computing to generate several 5 μm ×5 μm realizations for different CNT volume fractions. These realizations are then analyzed using finite elements to obtain volume averaged effective values, which are then subsequently used to generate measures of central tendency (estimated mean) and variability (standard deviation, coefficient of variation, skewness and kurtosis) in a descriptive statistical analysis. / Doctor of Philosophy / Carbon nanotubes or CNTs belong to a class of novel materials known as nanomaterials which are materials with length scales on the order of nanometers. CNTs have been widely studied due to their unique mechanical, electrical and thermal properties in comparison to traditional materials such as metals or plastics. Often times, research and applications concerning the use of CNTs involves embedding the CNTs as a filler within a larger composite material system. In the present work, CNTs are considered to be embedded within a polymer. It is known that the electrical properties of such a CNT/polymer composite change in response to the application of a mechanical force. This change in electrical properties is caused due to the presence of CNTs and is used as a means of sensing the mechanical state of the composite, i.e. real time structural monitoring. The extent of the change in electrical properties, also known as sensing, depends upon a number of different factors such as the amount of CNTs used per unit volume of the polymer, how well dispersed or clumped together the CNTs are within the polymer and the type of polymer material used, among other factors. A statistical analysis is performed with several case studies where these factors are varied and the resulting change in the sensing response is monitored. Several important conclusions were made from the statistical analysis with some of the results providing new insights into the sensing behavior of CNT/polymer composites. For example, it was found that a key parameter known as barrier potential, which directly influences the extent of sensing achieved through a mechanism known as electrical tunneling, needs to be several orders of magnitude lower than previously reported values to accurately capture the sensing effects. Key metrics quantifying the extent of sensing from the analysis were found to be in agreement with previously reported experimental results. The significance of such a statistical study lies in the fact that CNT embedded composites are increasingly being proposed and used for sensing applications. The use of CNT embedded polymers to encase explosive crystalline grains such as HMX or RDX is one such example. These explosive grains are used in a number of different civil and military applications such as fuel rocket propellants, industry explosives, military munitions etc. The grains possess extremely high energy densities and are susceptible to undergo violent chemical reaction if a trigger is provided through thermal or mechanical means. As such, the monitoring of the structural state of these explosives is crucial for their safe handling and processing. In this work, the sensing response of a composite material comprising of explosive grains surrounded by polymer material containing CNTs is studied in response to different types of mechanical loads, ranging from mild stimuli to impact. It was found that the sensing mechanism was capable of tracking mechanical damage as well as the resulting temperature increases interior to the composite. In addition to its application to safety and preventative measures, the use of CNTs in this context also provided insight into the mechanisms related to the sudden release of energy in these explosive grains which is of significant interest since this is an active area of research as well.

<p>Poli(mlečna kiselina) (PLA) predstavlja jedan od najpopularnijih komercijalnih biorazgradivih polimera. Iako može da zameni neke od najče&scaron;će kori&scaron;ćenih sintetskih polimera, neka njegova svojstva (lo&scaron;a barijerna, termička i mehanička) jo&scaron; uvek predstavljaju prepreku u &scaron;iroj primeni, posebno za pakovanje hrane. Jedan od najsavremenijih načina prevazilaženja nedostataka u svojstvima biopolimera predstavljaju nanotehnologije.<br />U ovom radu ispitan je uticaj dodatka različitih koncentracija hidrofobnih nanočestica silicijum (IV) oksida (od 0.2 mas.% do 5 mas.%) pripremom uzoraka u rastvoru, i rastopu na toplotna, mehanička, i barijerna svojstva PLA. Morfolo&scaron;ke karakteristike uzoraka nanokompozita snimljene su pomoću skenirajuće elektronske mikroskopije (SEM). Ostvarena je izuzetno dobra disperzija i distribucija hidrofobnih čestica silicijum (IV) oksida koje su u malim udelima dodavane u poli(mlečnu kiselinu). Dobra disperzija i distribucija hidrofobnih čestica silicijum (IV) oksida ostvarena je kako pripremom nanokompozita metodom u rastvoru, tako i metodom u rastopu.<br />Toplotna svojstva PLA i pripremljenih nanokompozita proučavana su primenom diferencijalnog skenirajućeg kalorimetra (DSC), dok je stepen kristalnosti određen rasipanjem X zraka pod &scaron;irokim uglom(WAXD). Mehanička svojstva su ispitivana da bi se odredio uticaj dodatka nanočestica SiO2 na prekidnu čvrstoću i izduženje čistog PLA. Iako su prilikom pripreme materijala metodom u rastvoru, pobolj&scaron;anja mehaničkih i barijernih svojstava postignuta pri udelima silicijum (IV) oksida u rasponu od 0,2 do 5 mas.%, najznačajnija pobolj&scaron;anja postignuta su za najmanje udele nanočestica (0,2 mas.% i 0,5 mas.%). Pobolj&scaron;anja mehaničkih i barijernih svojstava nanokompozita, primenjenih metodom u rastopu, su registrovana i za udele silicijum (IV) oksida od 0,2 do 3 mas.%.<br />Takođe je ispitana mogućnost primene pripremljenog nanokompozita na osnovu poli(mlečne kiseline) i silicijum (IV) oksida za pakovanje prehrambenih proizvoda na primeru pakovanja svežeg svinjskog mesa (M. longissimus thoracis et lumborum). Ispitivanjem uticaja materijala za pakovanje svežeg mesa u vakuumu, na parametre tehnolo&scaron;kog (pH, boja), senzorskog, i mikrobiolo&scaron;kog kvaliteta mesa, utvrđeno je da su PLA kao i nanokompoziti na osnovu PLA sa različitim udelima silicijum (IV) oksida, pogodni za vakuum pakovanje i skladi&scaron;tenje svežeg svinjskog mesa.</p> / <p>Poly(lactic acid) presents one of the most popular bio-polymers for diverse applications. However, the use of PLA as food packaging material is limited due to poor barrier and mechanical properties. These properties could be improved by incorporation of nanoparticles into polymer matrix.<br />In this work neat PLA films and PLA films with different percentage of hydrophobic fumed silica nanoparticles (0,2 wt.% to 5 wt.%) were prepared by solution casting and melt blending methods. Several procedures were used to characterize the influence of different silica content on dispersion (SEM), crystalline behavior (WAXD), thermal stability (DSC, TGA), mechanical and barrier properties. It is shown that the applied techniques and selection of specific hydrophobic spherical nanofiller provide a good dispersion and distribution of silica nanoparticles in poly(lactic acid) for both film preparation methods.<br />Characteristics of films prepared by solution casting method showed improvements in mechanical and barrier properties for all loadings of nanofiller but the most significant improvements were achieved for lowest silica content (0,2 wt.% and 0,5 wt.%) The improvements in material characteristics (mechanical and barrier) for melt blending method were also achieved (for concentrations from 0,2 wt.% to 3 wt.%).<br />After film preparation, selected cuts of M. longissimus thoracis et lumborum were packed in prepred films of polymer nanocomposites, and the shelf-life characterisation was conducted on technological, sensory and microbiological paramethers of quality. After shelf-life characterisation it can be concluded that polymer nanocomposites based on PLA and silica nanoparticles could be used for packaging od fresh pork meat in vacuum.</p>

The ability to convert photons into mechanical motion is of significant importance for many energy conversion and reconfigurable technologies. Establishing an optical-mechanical interface has been attempted since 1881; nevertheless, only few materials exist that can convert photons of different wavelengths into mechanical motion that is large enough for practical import. Recently, various nanomaterials including nanoparticles, nanowires, carbon nanotubes, and graphene have been used as photo-thermal agents in different polymer systems and triggered using near infrared (NIR) light for photo-thermal actuation. In general, most photomechanical actuators based on sp bonded carbon namely nanotube and graphene are triggered mainly using near infra-red light and they do not exhibit wavelength selectivity. Layered transition metal dichalcogenides (TMDs) provide intriguing opportunities to develop low cost, light and wavelength tunable stimuli responsive systems that are not possible with their conventional macroscopic counterparts. Compared to graphene, which is just a layer of carbon atoms and has no bandgap, TMDs are stacks of triple layers with transition metal layer between two chalcogen layers and they also possess an intrinsic bandgap. While the atoms within the layers are chemically bonded using covalent bonds, the triple layers can be mechanically/chemically exfoliated due to weak van der Waals bonding between the layers. Due to the large optical absorption in these materials, they are already being exploited for photocatalytic, photoluminescence, photo-transistors, and solar cell applications. The large breaking strength together with large band gap and strong light- matter interaction in these materials have resulted in plethora of investigation on electronic, optical and magnetic properties of such layered ultra-thin semiconductors. This dissertation will go in depth in the synthesis, characterization, development, and application of two- dimensional (2D) nanomaterials, with an emphasis on TMDs and molybdenum disulfide (MoS2), when used as photo-thermal agents in photoactuation technologies. It will present a new class of photo-thermal actuators based on TMDs and hyperelastic elastomers with large opto-mechanical energy conversion, and investigate the layer-dependent optoelectronics and light-matter interaction in these nanomaterials and nanocomposites. Different attributes of semiconductive nanoparticles will be studied through different applications, and the possibility of globally/locally engineering the bandgap of such nanomaterials, along with its consequent effect on optomechanical properties of photo thermal actuators will be investigated. Using liquid phase exfoliation in deionized water, inks based on 2D- materials will be developed, and inkjet printing of 2D materials will be utilized as an efficient method for fast fabrication of functional devices based on nanomaterials, such as paper-graphene-based photo actuators. The scalability, simplicity, biocompatibility, and fast fabrication characteristics of the inkjet printing of 2D materials along with its applicability to a variety of substrates such as plastics and papers can potentially be implemented to fabricate high-performance devices with countless applications in soft robotics, wearable technologies, flexible electronics and optoelectronics, bio- sensing, photovoltaics, artificial skins/muscles, transparent displays and photo-detectors.

<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>