Today, the majority of materials used for single-use packaging are petroleum-based synthetic polymers. With increased concern about the environmental protection, efforts have been made to develop alternative biodegradable materials from renewable resources. Starch offers an attractive alternative since it is of low cost and abundant. However, the starch material is brittle without plasticizer and the mechanical properties of starch materials are highly sensitive to moisture. In nature, the plant cell walls combine mechanical stiffness, strength and toughness despite a highly hydrated state. This interesting combination of properties is attributed to a network based on cellulose microfibrils. Inspired by this, microfibrillated cellulose (MFC) reinforced starch-based nanocomposites films and foams were prepared. Films with a viscous matrix and MFC contents from 10 to 70wt% were successfully obtained by solvent casting. The films were characterized by DSC, DMA, FE-SEM, XRD, mercury density measurements, and dynamic water vapor sorption (DVS). At 70wt% MFC content a high tensile strength together with high modulus and high work of fracture was observed. This was due to the nanofiber and matrix properties, favourable nanofiber-matrix interaction, a good dispersion of nanofibers and the MFC network. Novel nanocomposite foams were obtained by freeze-drying aquagels prepared from 8wt% solutions of amylopectin starch and MFC. The MFC content was varied from 10 to 70wt%. For composite foam with MFC contents up to 40wt%, improved mechanical properties were observed in compression. The mechanical properties depended both on the cell wall properties and the cell-structure of the foam. The effect of moisture (20-80% RH) on the dynamical properties of composite foam with 40wt% MFC was also investigated and compared to those of neat starch foam. Improved storage modulus was noted with MFC content, which was a result of the nanofiber network in the cell-wall. In addition, the moisture content decreased with MFC content, due to the less hydrophilic nature of MFC. / QC 20101118

The focus of this study was to explore process-structure-property relationships in biodegradable polymer nanocomposite films in order to eliminate the commonly used trial and error approach to materials design and to enable manufacturing of composites with tailored properties for targeted applications. The nanofiller type and concentration, manufacturing method and compounding technique, as well as processing conditions were systematically altered in order to study the process-structure-property relationships. Polylactic acid (PLA) was used as the polymer and exfoliated graphite nanoplatelets (GNP), carbon nanotubes (CNT), and cellulose nanocrystals (CNC) were used as reinforcement. The nanocomposite films were fabricated using three different methods: 1) melt compounding and melt fiber spinning followed by compression molding, 2) solution mixing and solvent casting, and 3) solution mixing and electrospinning followed by compression molding. Furthermore, the physical properties of the polymer, namely the crystallization characteristics were altered by using two different cooling rates during compression molding. The electrical response of the composite films was examined using impedance spectroscopy and it was shown that by altering the physical properties of the insulating polymer matrix, increasing degree of crystallinity, the percolation threshold of the GNP/PLA films is significantly reduced. Additionally, design of experiments was used to examine the influence of nanofiller type (CNT versus GNP), nanofiller content, and processing conditions (cooling rate during compression molding) on the elastic modulus of the composite films and it was concluded that the cooling rate is the primary factor influencing the elastic modulus of both melt compounded CNT/PLA and GNP/PLA films. Furthermore, the effect of nanofiller geometry and compounding method was examined and it was shown that the high nanofiller aspect ratio in the CNT/PLA films led to decreased percolation threshold compared to the GNP/PLA films. The melt compounded GNP/PLA films displayed a lower percolation threshold than the solution cast GNP/PLA films most likely due to the more homogeneous distribution and dispersion of GNP in the solution cast films. Fully biodegradable and biorenewable nanocomposite films were fabricated and examined through the incorporation of CNC in PLA. Through the addition of CNC, the degree of crystallinity of the matrix was significantly increased. Focusing the design space through investigation of process-structure-property relationships in PLA nanocomposites, can help facilitate nanocomposites with tailored properties for targeted applications.

Substances that consist of nano-scale fillers dispersed in a polymer matrix are known as polymer-nanocomposites (PNCs). These materials are appealing since they have high potentials for applications, due to their mechanical, electrical, and thermo electrical properties. A common problem associated with PNCs is that the nano-fillers have a tendency to aggregate into clusters and form phase separated domains, which cause the desired properties of the system to either diminish or vanish all together. Hairy nanoparticles (HNPs) can avoid the issue of agglomeration that is commonly encountered by conventional PNCs. When polymer chains are grafted to a nanoparticle, and the coverage is high, the nanoparticles have decreased inter-particle interactions which allows for enhanced dispersion and mixing into a polymer matrix. By tailoring the architecture (functionalization of polymer chains, degree of polymerization, grafting density) of HNPs, it is possible to control the final properties of the system. An in depth study was carried out to investigate the effects of hairy-nanoparticle architecture on the resulting properties of the material itself. Atom transfer radical polymerization and living anionic polymerization were used to synthesize the polymer chains, of the HNP systems, while various instrumental methods including differential scanning calorimetry (DSC) and scanning electron microscopy (SEM) were utilized to study the physical ageing affects and self-assembly of these systems. #88ABW-2015-4971

chemical partitioning of Cobalt-containing soft magnetic amorphous and nanocomposite materials has been investigated with particular focus on its consequences on these materials’ nanostructure and electrical resistivity. Theory, models, experiment, and discussion in this regard are presented on this class of materials generally, and are detailed in particular on alloys of composition, (Fe65Co35)79.5+xB13Si2Nb4-xCu1.5, for X={0- 4at%}, and Co-based, Co76+YFe4Mn4-YB14Si2Nb4, for Y={0-4at%}. The context of this work is within the ongoing efforts to integrate soft magnetic metal amorphous and nanocomposite materials into electric motor applications by leveraging material properties with motor topology in order to increase the electrical efficiency and decrease the size, the usage of rare-earth permanent magnets, and the power losses of electric motors. A mass balance model derived from consideration of the partitioning of glass forming elements relates local composition to crystal state in these alloys. The ‘polymorphic burst’ onset mechanism and a Time-Temperature- Transformation diagram for secondary crystallization are also presented in relation to the partitioning of glass forming elements. Further, the intrinsic electrical resistivity of the material is related to the formation of virtual bound states due to dilute amounts of the glass forming elements. And lastly, a multiphase resistivity model for the effective composite resistivity that accounts for the amorphous, crystalline, and glass former-rich amorphous regions, each with distinct intrinsic resistivity, is also presented. The presented models are validated experimentally on the Co-containing alloys by Atom Probe Tomography performed through collaboration with Pacific Northwestern National Laboratory.

The rapid development of polymer nanocomposites has received extensive attention over the last few decades. The ability to alter functionalities of composites, dramatically improving properties and performance at low filler content creates flexibility in designing materials for advanced applications in various industrial fields. This work focuses on nanocomposites relevant to the packaging and aerospace industries. This work evaluated the ability to homogeneously distribute nanomaterials into a polymer matrix, understand the effects on rheological properties, understand changes to microstructure and effects, and characterize properties of resulting nanocomposite. High torque melt mixing was used to disperse surface modified cellulose nanocrystals in a poly(lactic acid) (PLA) resin and graphene in a phenylethynyl terminated imide resin, PETI 298, using bulk graphite. Rheology, Raman spectroscopy, and X-Ray powder diffraction were applied for the understanding of changes to the microstructure and location of optimum loading by the determination of the percolation threshold. Thermomechanical performance was evaluated through TGA, DMA, and DSC. It was determined that graphene and short stacks of graphene could be dispersed and distributed at low loadings in PETI 298. As expected, the addition of graphitic material led to an increase in viscosity, but also caused a retardation of the cure which could be attributed to increased viscosity or quenching of free radicals. Changes to the microstructure were difficult to evaluate because of the competing chemistry occurring in the system but it could be determined that something significant occurs around 1 wt % at which the melt rheology and the microstructure behavior was different from other composites. It was further determined that the melt mixing process led to the formation of an ordered structured. Modification of the cellulose nanocrystals (m-CNC) with Cardura, glycidyl ester, provided no improvement to mechanical properties of PLA composites. However, m-CNCs were found to nucleate the crystallization of PLA. Lack of improvement to mechanical properties could be attributed to the degradation of polymer during processing.

Carbon nanotubes are known as ideal fillers for polymer systems; the main advantage of carbon nanotubes over other nano-reinforcing particles is the combination of superior strength and stiffness with large aspect ratio. Carbon nanotubes may improve the mechanical, electrical and thermal properties of polymers, but to realise their potential in polymer systems uniform dispersion, strong interfacial adhesion and alignment of nanotubes within the polymer matrix are necessary. These properties are not easy to achieve and they are key challenges in producing CNT/Polymer system. This research was carried out in an attempt to understand how the properties of CNT/Polymer composite can be optimised by manipulation of additives, compounding and postcompounding conditions. Polypropylene/Multi-Walled Carbon Nanotube (PP/MCNT) composites were prepared by conventional twin screw extrusion. Dispersants and compatibilisers were used to establish good interaction between filler and polymer. Several different extruder screw configurations were designed and the properties of PP/MCNT composite prepared by each configuration investigated. The results indicated that the addition of carbon nanotubes without additives enhanced mechanical, electrical and thermal properties of polypropylene polymer. Incorporation of compatibilisers into PP/MCNT improved the stiffness but decreased the strength of the nanocomposite, whilst addition of dispersants decreased the mechanical properties of the nanocomposite. Addition of both additives at high concentration improved electrical conductivity and induced electrical percolation in the nanocomposite. Extruder screw configuration was found to have significant effect on the electrical conductivity whilst only slightly affecting mechanical properties of the nanocomposite, possibly due to the competition between dispersion and degradation of polymer chains and possible reduction of carbon nanotube length by intensive shear during compounding. The use of screw configuration with high mixing intensity promoted the dispersion of nanotubes and favoured the conduction process in the nanocomposite. Finally in an attempt to improve dispersion and alignment of carbon nanotubes, compounded PP/MCNT composite was subjected to micromoulding, fibre spinning and biaxial stretching processes and the resultant properties investigated. Application of post-compounding process was found to have significant effect on mechanical and rheological properties of the nanocomposite. Stiffness and strength of the nanocomposites treated by post-compounding processes were found to increase by up to 160% and 300%, respectively. The reinforcement effect of carbon nanotubes in the stretched nanocomposites was found to be the greatest. Rheological analysis suggested that the application of post-compounding processes enhanced dispersion of carbon nanotubes within the nanocomposite. Overall, this finding of this research has shown that carbon nanotubes can be incorporated into polypropylene using conventional equipment to provide significant improvement in properties. By careful choices of additives, compounding and postcompounding conditions, specific properties can be further enhanced.

La présence de bactéries et biofilms est une préoccupation permanente dans de nombreux domaines. Ils sont à l’origine de nombreux faits d’actualité qui ont un coût important pour le système de santé. L’objectif de notre travail visait à élaborer des films nanocomposite transparents contenant des particules métalliques nanométriques d'élément antibactérien (Ag ou Cu) immergées dans une matrice d’oxyde (TiO₂). La méthode de dépôt DLI-MOCVD (Direct Liquid Injection-Metal Organic Chemical Vapor Deposition) a été employée pour élaborer les films composites. Ce procédé permet le contrôle de la fraction molaire des précurseurs injectés dans le réacteur CVD et de revêtir des supports 3D (poreux). La croissance et la structure du dioxyde de titane (TiO₂) sont influencées par la présence du précurseur contenant l’élément antibactérien. La fraction molaire du précurseur (Ag ou Cu) modifie les caractéristiques physico chimiques et structurales des dépôts. L'activité antibactérienne est mesurée selon la norme JIS Z 2801:2000 avec S. aureus et E. coli en l’absence de lumière. Des essais antibactériens spécifiques ont été optimisés afin d'évaluer leur activité proche de condition réelle. La composition des dépôts influence fortement l’activité antibactérienne d’inactif à bactéricide. Des corrélations entre la microstructure et la composition des films et leurs propriétés antibactériennes sont discutées. / The presence of bacteria and biofilms is permanent concern in many fields. Their presences are at the origin of many events which have high costs for the health system. In this objective, this work aimed to elaborate transparent nanocomposite thin films which are composed of nanometric metallic particles of antibacterial element (Ag or Cu) embedded in an oxide matrix (TiO₂). The DLI-MOCVD process (Direct Liquid Injection-Metal Organic Chemical Vapour Deposition) was used to elaborate these thin films. This process allows the quantity of precursors injected into the CVD reactor to be controlled and porous body to be coated. The growth mechanisms and the structure of the Titanium dioxide (TiO₂) are influenced by the presence of the organic precursor which contains the antibacterial element. The mole fraction of precursor (Ag or Cu) modifies the physico-chemical and structural properties of films. The antibacterial activity was tested according to the standard JIS Z 2801: 2000 with S. aureus and E. coli without light Specific tests were optimised in order to evaluate their activity in environments more representative. The composition of coatings impacts strongly the antibacterial activities from inactive to bactericidal properties. Correlations between the microstructure and composition of films and their antibacterial properties are discussed.

Thesis advisor: Zhifeng Ren / Thermoelectrics, as one promising approach for solid-state energy conversion between heat and electricity, is becoming increasingly important within the last a couple of decades as the availability and negative environmental impact of fossil fuels draw increasing attention. Therefore, various thermoelectric materials in a wide working temperature range from room temperature to 1000 degrees Celsius for power generation or below zero for cooling applications have been intensively studied. In general, the efficiency of thermoelectric devices relies on the dimensionless figure-of-merit (ZT) of the material, defined as ZT=(S<super>2</sup>&sigma;)T/&kappa;, where S is the Seebeck coefficient, [sigma] the electrical conductivity, [kappa] the thermal conductivity (sum of the electronic part, the lattice part, and the bipolar contribution at high temperature region), and T the absolute temperature during operation. Techniques to measure those individual parameters will be discussed in the 2nd chapter while the 1st chapter mainly covers the fundamental theory of thermoelectrics. Recently, the idea of using various nanostructured materials to further improve the ZT of conventional thermoelectric materials has led to a renewed interest. Among these types of nanostructured materials, nanocomposites which mainly denote for the nano-grained bulk materials or materials with nano-sized inclusions are the major focus of our study. For nanocomposites, the enhancement in ZT mainly comes from the low lattice thermal conductivity due to the suppressed phonon transport by those interfaces or structure features in the nanometer scale without deteriorating the electron transport. In the last few years, we have successfully demonstrated in several materials systems (Bismuth Telluride, Skutterudites, Silicon Germanium) that ball milling followed by hot pressing is an effective way for preparing large quantities of those nanocomposite thermoelectric materials with high ZT values in the bulk form. Therefore, in the 3rd part of this thesis, I will talk about how I applied the same technique to the Thalllium (Tl) doped Lead Telluride (PbTe) which was reported for an improved Seebeck coefficient due to the creation of resonant states near the Fermi level, leading to a high ZT of about 1.5 at around 500 degrees Celsius. I showed that comparing with conventional tedious, energy consuming melting method, our fabrication process could produce such material with competing thermoelectric performance, but much simpler and more energy effective. Potential problems and perspectives for the future study are also discussed. The 4th chapter of my thesis deals with the challenge that in addition to those nanostructuring routes that mainly reduce the thermal conductivity to improve the performance, strategies to enhance the power factor (enhancing [sigma] or S or both) are also essential for the next generation of thermoelectric materials. In this part, modulation-doping which has been widely used in thin film semiconductor industry was studied in 3-D bulk thermoelectric nanocomposites to enhance the carrier mobility and therefore the electrical conductivity [sigma]. We proved in our study that by proper materials design, an improved power factor and a reduced thermal conductivity could be simultaneously obtained in the n-type SiGe nanocomposite material, which in turn gives an about 30% enhancement in the final ZT value. In order to further improve the materials performance or even apply this strategy to other materials systems, I also provided discussions at the end of chapter. In the last chapter, the structural and transport properties of a new thermoelectric compound Cu₂Se was studied which was originally regarded as a superionic conductor. The [beta]-phase of such material possesses a natural superlattice-like structure, therefore resulting in a low lattice thermal conductivity of 0.4-0.5 Wm^-1K^-1 and a high peak ZT value of ~1.6 at around 700 degrees Celsius. I also studied the phase transition behavior between the cubic [beta]-phase and the tetragonal [alpha]-phase of such material from the discontinuity of transport property curves and the change in crystal structure. In addition, I also talk about the abnormal decrease in specific heat with increasing temperature that I observed in the as-prepared Cu₂Se samples. I suggest this material is of general interest to a broad range of researchers in Physics, Chemistry, and Materials Science. / Thesis (PhD) — Boston College, 2012. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Physics.

Dentre os materiais de fontes naturais e renováveis, a celulose se destaca pela sua abundância, podendo ser encontrada em diversos organismos vivos, como plantas, amebas, bactérias, fungos e alguns animais marinhos. Suas dimensões podem ser reduzidas por quebra das cadeias amorfas, com possibilidade de atingir escalas nanométricas, obtendo-se assim as chamadas nanopartículas de celulose ou nanocelulose. Devido à alta cristalinidade, a nanocelulose possui altos valores de módulo elástico, proporcionando alta capacidade de reforço em matrizes poliméricas, combinados com baixo peso, área superficial elevada e biodegradabilidade. A borracha natural é uma matéria-prima de fonte natural, sendo extraída das seringueiras na forma de látex - dispersão coloidal de partículas de borracha e substâncias não-borrachas em um meio aquoso, com aspecto leitoso. No presente trabalho foram estudados compósitos de borracha natural e nanocelulose. Inicialmente, foi realizada uma análise do látex de nacionalidade brasileira, centrifugado, contendo 60% em massa de sólidos. Os resultados de caracterização do látex centrifugado comercial, a qual consistiu na análise de concentração de sólidos totais e na medida do pH, estavam de acordo com os dados apresentados pelo fornecedor. Além disso, a análise de distribuição de tamanho de partícula indicou que o material apresenta uma população, com tamanho médio de 1,0 ?m. A borracha coagulada com ácido acético apresentou, após mastigação em cilindro aberto, viscosidade Mooney e extrato acetônico igual a, respectivamente, 52,8 e 2,57%. As nanoceluloses foram obtidas por hidrólise com ácido ortofosfórico (NC P) e sulfúrico (NC S), sendo classificadas como nanocristal de celulose (NC). NC P apresentaram comprimento médio, razão de aspecto e cristalinidade igual a, respectivamente, 270 ± 89 nm, 50 ± 24 e 78%; e as NC S apresentaram 209 ± 51 nm, 29 ± 10 e 75%.. Os compósitos de borracha natural com nanocristais de celulose apresentaram, nos ensaios de tração, aumentos nos valores de todas as propriedades analisadas, quando comparados à borracha natural pura. Ao adicionar-se 10 phr de nanocelulose preparada com ácido fosfórico na borracha natural, os valores de resistência à tração na ruptura, alongamento na ruptura e módulo a 300% aumentaram, respectivamente, em 90%, 16% e 52%. Já com a adição de 10 phr de NC S, essas propriedades aumentaram, respectivamente, em 68%, 5% e 109%. O mesmo foi observado para a dureza Shore A. Com a adição de 10 phr de nanocelulose obtida por ácido fosfórico à composição da borracha natural, a dureza Shore A aumentou em cerca de 22%; já com a adição de 10 phr de NCs S, a dureza da borracha natural aumentou em 36%. / Among the natural and renewable sources\' materials, cellulose stands out for its abundance, it can be found in many living organisms, such as plants, amoebas, bacteria, fungi and some marine animals. Its dimensions can be reduced by breaking the amorphous chains, with the possibility of reaching nanometric scales, obtaining the nanocellulose or cellulose nanoparticles. Due to the high crystallinity, the nanocellulose has high elastic modulus value, providing high reinforcement capacity combined with low weight, high surface area and biodegradability. Natural rubber is a raw material from a natural source, extracted from the latex - colloidal dispersion of rubber particles and non-rubbers in a milkylooking aqueous solution. At this work, composites of natural rubber and nanocellulose were studied. Initially, a Brazilian centrifuged latex with 60% of its weight in solids was characterized, by analyzing if the total solids concentration and the pH measurement is in agreement with the data presented by the supplier. In addition, particle size distribution analysis demonstrated that the material had an average size of 1.0 ?m. Then, the mastication in the open cylinder and the Mooney viscosity and acetone extract was measured and them were equal to, respectively, 52.8 and 2.57%. The nanocelluloses obtained by hydrolysis with phosphoric and sulfuric acids are classified as cellulose nanocrystal. NC P present average length, aspect ratio and crystallinity equal to 270 ± 89 nm, 50 ± 24 and 78%; and the NC S had 209 ± 51 nm, 29 ± 10 and 75%. In the tensile test, it was observed that there was an increase in all the mechanical properties analyzed for natural rubber when adding the nanocellulose in its composition. By adding 10 phr of prepared nanocellulose with phosphoric acid in the natural rubber the values of tensile strength at rupture, strain at rupture and modulus at 300% increased, respectively, by 90%, 16% and 52%. When added 10 phr of NC S, these properties increased, respectively, by 68%, 5% and 109%. The same was observed for Shore A hardness. When adding 10 phr of nanocellulose obtained by phosphoric acid in its composition, the Shore A hardness increased by about 22%; When adding 10 phr of NCs S, the hardness increased by 36%.

Este trabalho aborda o estudo do comportamento mecânico, térmico e reológico do nanocompósito de HMSPP polipropileno de alta resistência do fundido (obtido por radiação gama na dose de 12,5 kGy) e uma argila brasileira bentonítica do Estado da Paraíba (PB), conhecida como chocolate com concentração de 5 e 10 % em massa em comparação a uma argila americana, Cloisite 20A. Foi utilizado nesse nanocompósito o agente compatibilizante polipropileno graftizado com anidrido maleico PP-g-AM com 3 % de concentração em massa, através da técnica de intercalação do fundido utilizando uma extrusora de dupla-rosca e, em seguida, os corpos de prova foram confeccionados em uma injetora. O comportamento mecânico foi avaliado pelos ensaios de tração, flexão e impacto. O comportamento térmico foi avaliado pelas técnicas de calorimetria exploratória diferencial (DSC) e termogravimetria (TGA). O comportamento reológico foi avaliado em um reômetro de placas paralelas. A morfologia dos nanocompósitos foi estudada pela técnica de microscopia eletrônica de varredura (MEV). As bentonitas organofílicas e os nanocompósitos foram caracterizados por difração de raios X (DRX) e infravermelho (FTIR). Nos ensaios mecânicos houve um aumento de 9 % na resistência à tração e no módulo de Young, para os nanocompósitos de HMSPPC com argila Cloisite 20A. No ensaio de impacto izod, o nanocompósito HMSPPB 10 % com argila chocolate obteve um aumento de 50 % na resistência ao impacto. / This work concerns to the study of the mechanical, thermal and rheological behavior of the nanocomposite HMSPP - high melt strength polypropylene (obtained at a dose of 12.5 kGy) and a Brazilian bentonite clay from State of Paraiba (PB), known as \"Chocolate\" in concentrations of 5 and 10 % by weight in comparison with one American clay, Cloisite 20A. The compatibilizer agent based on maleic anhydride grafted polypropylene, known as PP-g-MA, was added at 3 % weight concentration through the melt intercalation technique using a twin-screw extruder, and afterwards, the specimens were prepared by injection process. The mechanical behavior was evaluated by strength, flexural strength and impact tests. The thermal behavior was evaluated by the differential scanning calorimetry (DSC) and thermogravimetry (TGA). The rheological behavior was evaluated in parallel-plate rheometer. The morphology of the nanocomposites was studied by the technique of scanning electron microscopy (SEM). The organophilic bentonite and the nanocomposites were characterized by X-ray diffraction (XRD) and infrared (FTIR). Results of mechanical tests showed a 9 % increase in the tensile strength and Young\'s modulus for the nanocomposites HMSPPC, with Cloisite 20A clay. The nanocomposite HMSPPB 10 %, with \"chocolate\" clay obtained a 50 % increase in the impact strength in the izod impact test.