Esta tese está dividida em duas partes. Na Parte I, blendas de polietileno maleado (M-PE) e butirato acetato de celulose (CAB) (5-50% em massa) e compósitos de polietileno (PE) ou M-PE e 20% em massa de celulose, acetato de celulose (CA), propionato acetato de celulose (CAP) ou CAB foram preparados em um misturador. As estruturas e propriedades das misturas foram estudadas através de ensaios mecânicos, calorimetria exploratória diferencial, microscopia eletrônica de varredura, extração com solvente seletivo seguida de espectroscopia FTIR e difração de raios-X (XRD). As blendas M-PE/CAB e os compósitos PE/polissacarídeo e M-PE/polissacarídeo não apresentaram mudanças significativas nos valores da temperatura de fusão (Tm) quando comparados aos valores de Tm do PE e do M-PE. Dados de XRD mostraram que a adição das cargas não causou mudança na estrutura cristalina do PE ou M-PE, mas aumentou a região amorfa dos materiais, indicado que a miscibilidade ocorre na parte amorfa do PE. Compósitos preparados com M-PE apresentaram tensão no escoamento e elongação superiores do que os preparados com PE, evidenciando o efeito compatibilizante do anidrido maléico. Na parte II, o efeito de dois bons solventes, acetona e acetato de etila, nas características e propriedades superficiais dos filmes finos (50nm&#60;espessura<200nm) e ultrafinos (espessura<6nm) de CA, CAP ou CAB preparados por revestimento rotacional ou adsorção, respectivamente, foram caracterizados por elipsometria, microscopia de força atômica (AFM) e medidas de ângulo de contato. Os resultados foram discutidos baseados na taxa de evaporação do solvente e na energia de interação substrato-solvente. Os efeitos do recozimento e do tipo de éster de celulose na espessura, morfologia e molhabilidade da superfície foram investigados. Após o recozimento, os filmes ultrafinos de ésteres de celulose tornam-se hidrofóbicos, indicando uma reorientação molecular na interface sólido-ar. Os filmes ultrafinos preparados a partir de soluções de acetona são estáveis, enquanto que os preparados a partir de soluções de acetato de etila apresentaram dewetting. A estabilidade dos filmes foi monitorada por AFM e explicada pelos valores da constante de Hamaker, determinados pela primeira vez para estes materiais. A imobilização de lipase sobre os filmes ultrafinos estáveis de CA, CAP e CAB com e sem recozimento foi quantificada para avaliar a possibilidade de aplicação destes filmes como substratos para biomoléculas. A adsorção de lipase sobre os filmes de CA e CAP com recozimento foi mais pronunciada do que nos mesmos filmes sem recozimento. A atividade enzimática da lipase foi avaliada com medidas espectrofotométricas do produto formado a partir da hidrólise do para-nitrofenol dodecanoato. A lipase imobilizada sobre os filmes mais hidrofóbicos apresentou uma atividade maior do que a lipase livre e manteve a atividade alta após três usos. As amostras foram estocadas por até 30 dias. A lipase imobilizada sobre os filmes mais hidrofóbicos manteve 70% da sua atividade, e a lipase imobilizada sobre os filmes mais hidrofílicos manteve apenas 30% da atividade. Estes resultados indicaram que preservação da estrutura conformacional da enzima foi favorecida pela hidrofobicidade do substrato polimérico e interações entre os resíduos polares da lipase e as partes de glucopiranosil dos ésteres de celulose. / This thesis is divided into two parts. In the first part, blends of maleated polyethylene (M-PE) and cellulose acetate butyrate (CAB) (5-50wt%) and composites of polyethylene (PE) or M-PE and 20wt% of cellulose, cellulose acetate (CA) or cellulose acetate propionate (CAP) were prepared in an laboratory mixer. The mixtures structures and properties have been studied by means of tensile testing, differential scanning calorimetry, scanning electron microscopy, X-ray diffraction (XRD) and extraction with a selective solvent followed by Raman spectroscopy. No significant change on the melting temperature (Tm) values obtained for M-PE/CAB blends or PE/polysaccharides or M-PE/polysaccharides composites could be observed, when compared with the Tm values obtained for PE and M-PE. X-ray diffraction showed that the addition of the polysaccharides had no influence on the lattice constants of PE or M-PE, but it increased the PE amorphous region, indicating that the miscibility happens on the amorphous region of the PE. Composites prepared with M-PE presented yield stress and elongation values higher than those prepared with PE, showing the compatibilizer effect of maleic anhydride. In the second part, the effect of two good solvents, acetone and ethyl acetate, on the characteristics and surface properties of thin (30nm&#60;thickness<200nm) and ultrathin (thickness<6nm) cellulose ester films obtained by spin coating or adsorption, respectively, has been investigated by means of ellipsometry, atomic force microscopy (AFM) and contact angle measurements. The results were discussed in the light of solvent evaporation rate and interaction energy between substrate and solvent. The effects of annealing and type of cellulose ester on film thickness, film morphology and surface wettability were also studied. Upon annealing, ultrathin films of cellulose ester became hydrophobic, evidencing molecular re-orientation at the solid-air interface. Ultrathin films prepared from acetone solutions are stable, but the ones prepared from ethyl acetate solutions presented dewetting. Film stability was followed by AFM and explained with basis on the Hamaker constant values, calculated for the first time for CA, CAP and CAB. The adsorption of lipase onto stable ultrathin films of cellulose esters, with and without annealing, was quantified in order to evaluate the possibility of applying such films as support for biomolecules. Lipase adsorption onto annealed CA and CAP films was more pronounced than that onto CA and CAP untreated films. Enzymatic activity was evaluated by the spectrophotometric measurement of the product formed from the hydrolysis of para-nitrophenyl dodecanoate. Lipase immobilized onto more hydrophobic films presented higher activity than free lipase and could be reused three times retaining activity at a high level. The effect of storing time on the activity of immobilized lipase was studied. Lipase immobilized onto more hydrophobic films retained 70% of activity after one month, reaching the same level of activity of free lipase, and lipase immobilized onto more hydrophilic films retained just 30% of activity after 30 days. These results indicated that enzyme preservation was favored by polymeric substrate hydrophobicity and by the interactions between the polar residues of lipase and the glucopyranosyl moieties of cellulose ester.

Les recherches portant sur le développement des composites réfractaires de type SiCf/SiC pour application gainage du combustible des réacteurs de géneration IV ont conduit le CEA à s’intéresser aucomportement thermique de ces matériaux. En particulier, la connaissance des propriétés thermiques représente un des points cles dans la conception des composants. Au regard du concept sandwichdont la complexité de structure et la géométrie cylindrique s'éloigne de celle d'éprouvettes planes classiquement utilisées, les méthodes de mesures usuelles ne conviennent pas.Ce travail de thèse s’intéresse à la caractérisation et à la modélisation du comportement thermiquede ces structures. Une première partie du travail concerne l'identification des paramètres thermiquesglobaux des différentes couches constitutives d'une gaine sandwich . Pour cela, une méthodeash est employée et un banc d’expériences adapte aux géométries tubulaires a pu être développe.L’écriture d'un nouveau modèle d'estimation, fonde sur le couplage des signaux recueillis à la fois enface avant et en face arrière, permet aujourd'hui d’accéder par la mesure a la diffusivité thermiquedes composites tubulaires via la thermographie infrarouge. Dans une seconde partie de la thèse,une démarche matériau virtuel a été mise en place pour décrire le comportement thermique d'unegaine sandwich à partir des propriétés des constituants élémentaires (bres et matrice). Cespropriétés, obtenues avec deux méthodes d'estimation différentes permettant d'exploiter les mesuresde deux expériences distinctes basées sur la thermographie infrarouge, sont utilisées comme donnéespour la modélisation du transfert thermique au sein de ces gaines. Les confrontations réalisées entrecampagnes de mesures et expériences numériques permettent normalement d’appréhender le poids desdifférents facteurs d'influence qui régissent les transferts thermiques. / Researches on the development on SiCf/SiC refractory composites for generation IV nuclear fuel cladding led the CEA to focus on the thermal behavior of these materials. In particular, knowingthe thermal properties is essential for their components design. Regarding the development of the sandwich" concept, whose complexity and geometry differ from the conventionally used at tubes,usual measurement methods are unsuitable.This PhD reports on the characterization and modeling of the thermal behavior of these structures. The first part concerns the identification of the global thermal parameters of the diferent layers of a"sandwich" sheath. To do so, a ash method is used and an experimental bench suitable for tubular geometries was developed. A new estimation method based on the combination of both collectedsignals in front and rear faces allows the identification of the thermal diffusivity of tubular composites using infrared thermography. The second part focuses on a virtual material approach, established todescribe the thermal behavior of a "sandwich" cladding, starting from the properties of the elementary components (bers and matrix). These properties, obtained using two different estimation methods,allows exploiting the measurements of two separate experiments based on infrared thermography.They are then used as data for the heat transfer modeling in these ducts. Confrontations betweenexperimental measurements and numerical results finally allow gaining insight into the in uence ofthe different key parameters governing the heat transfer.

Biocomposites made from biodegradable polymer as matrix and natural fiber as reinforcement are certainly environmentally friendly materials. Both constituent materials are fully biodegradable and do not leave any noxious components on Earth. The natural fibers have been used as reinforcement due to their advantages compared to glass fibers such as low cost, high specific strength and modulus, low density, renewability and biodegradability. Major aims of this work were to produce natural fibers and/or nanoparticles with polyethylene (PE), polypropylene (PP) and polylactide (PLA), poly(hydroxybutyrate-co-hydroxyvalerate)(PHBV) matrices and determine their structure-property relationships. Following abstracts of the present research work are manifold: BINARY COMPOSITES Polylactide (PLA)/flax mat composites The polylactide (PLA)/flax mat and modified PLA/flax mat composites were produced by hot press technique. Two additives of non-regulated wax/ethylene acrylate copolymer/butyl acrylate and acrylic were used as modifier for PLA. The dispersion of the flax mat in the composites was studied by scanning electron microscopy (SEM). The PLA composites were subjected to instrumented falling weight impact test. The mechanical and thermal properties of the composites were determined in tensile test, thermogravimetric analysis (TGA) and dynamic-mechanical thermal analysis (DMTA), respectively. It was found that the PLA based composites increased the impact resistance. The tensile strength value of modified PLA/flax mat composite decreased slightly compared to the PLA. The elongation at break data indicated that an improvement in ductility of modified PLA and its composites. Moreover, addition of thermal modifier enhanced thermal resistance below processing temperature of PLA and had a marginal effect on the glass transition temperature of PLA. The storage modulus master curves were constructed by applying the time-temperature superposition (TTS) principle. The principle of linear viscoelastic material was fairly applicable to convert from the modulus to the creep compliance for all systems studied. Polylactide (PLA)/woven flax textiles composites The polylactide (PLA)/woven flax textiles 2x2 twill and 4x4 hopsack composites were produced by interval hot press technique. Two weave styles of flax used to reinforce in PLA. The dispersion of the flax composite structures in the composites was inspected in scanning electron microscopy (SEM). The PLA composites were subjected to instrumented falling weight impact test. The mechanical properties (tensile, stiffness and strength) of the composites were determined in tensile and dynamic-mechanical thermal analysis (DMTA) tests, respectively. SEM observed that the interfacial gaps around pulled-out fibers were improved when produced by the interval hot press. It was also found that the both styles of flax composites increased the impact resistance compared to the neat PLA. The tensile strength and stiffness value of PLA/flax composites were markedly higher than that of the neat PLA and reflect the effects of composite structures. The calculated storage creep compliance was constructed by applying the time-temperature superposition (TTS) principle. The calculated creep response of these flax composites was much lower than that of the neat PLA. Polyethylene and polypropylene/nano-silicon dioxide/flax composites Composites composed of polylactide (PLA), modified PLA and woven flax fiber textiles (Flax weave style of 2x2 twill and 4x4 hopsack) were produced by hot press technique. Two structurally different additives used to modify PLA. The dispersion of the flax composite structures in the composites was studied by scanning electron microscopy (SEM) and computed microtomography system (µCT). The PLA composites were subjected to water absorption and instrumented falling weight impact tests. The thermomechanical and creep properties of the composites were determined in thermogravimetric analysis (TGA), dynamic-mechanical thermal analysis (DMTA)and short-time creep tests, respectively. It was found that the modified PLA and its composite increased the impact resistance compared to the unmodified PLA. Incorporation of flax decreased resistance to thermal degradation and increased water uptake. The impact energy and stiffness value of PLA/flax composites was markedly higher than that of PLA but reflect the effects of composite structures and flax content. The storage modulus master curves were constructed by applying the time-temperature superposition (TTS) principle. From the master curve data, the effect of modified PLA on the storage modulus was more pronounced in the low frequencies range. Polylactide (PLA)/woven flax fiber textiles/boehmite alumina (BA) composites The textile biocomposites made from woven and non-woven flax fibre reinforced poly(butylene adipate-co-terephthalate) (PBAT) were prepared by compression moulding using film stacking method. The mechanical properties (such as tensile strength and stiffness, flexural strength and modulus, and impact strength) of textile biocomposites were determined in tensile, flexural and impact tests, respectively. The PBAT-based composites were subjected to water absorption. The comparison of the mechanical properties was made between pure PBAT and textile composites. The influence of flax weave styles on the mechanical properties was also evaluated. The results showed that the strength of the textile biocomposites was increased according to weave types of fibers, especially in the stiffness was significantly increased with the higher densification of the fibers. The 4x4-plain woven fibers (4-yard-wrap and 4-yard-weft weave direction) reinforced biocomposite indicated the highest strength and stiffness compared to the other textile biocomposites and pure PBAT. This was considered to be as the result of the character of weave style of 4x4-plain woven fibers. The aminopropyltriethoxysilane affected the mechanical properties and water absorption of the resulting composites laminates due to the surface compatibility between flax fiber and PBAT. HYBRID COMPOSITES Polyethylene/nanoparticle, natural and animal composites Binary and ternary composites composed of high-density polyethylene (HDPE), boehmite alumina (BA) and different kinds of natural-, animal fibers, like flax, sponge gourd (SG), palm and pig hair (PH) were produced by hot press technique. Aqueous BA suspensions were sprayed on the HDPE/flax mat to prepare nanoparticle/natural fiber reinforced ternary polymer composites followed by drying. The dispersion of the natural-, animal fibers and BA particles in the composites was studied by scanning electron microscopy (SEM) and discussed. The thermomechanical and stress relaxation properties of the composites were determined in thermogravimetric analysis (TGA), dynamic-mechanical thermal analysis (DMTA) and short-time stress relaxation tests (performed at various temperatures), respectively. The HDPE based composites were subjected to water absorption and instrumented falling weight impact tests. It was found that the all composites systems increased the stiffness, stress relaxation and reduced the impact toughness. The stress relaxation modulus of natural-, animal fiber composites were higher compared to that of the neat HDPE. This modulus increased greatly with in corporation of BA. The relaxation master curves were constructed by applying the time-temperature superposition (TTS) principle. The inverse of Findley power law could fairly applicable to describe the relaxation modulus vs. time traces for all systems studied. Incorporation of BA particles enhanced the thermal resistance which started to degrade at higher temperature compared to the HDPE/flax mat composite. The HDPE/flax mat/BA composite could reduce the water uptake. Polyethylene/Flax/SiO2 Composites Composites composed of high-density polyethylene (HDPE), woven flax fiber textiles (Flax weave style of 2x2 twill and 4x4 hopsack) and silicon dioxide (SiO2) were produced by hot press with nano spraying technique. The SiO2 slurries were sprayed by a hand onto the both surface of the woven flax fiber. The HDPE /woven flax fibers composites with and without used nano-spraying technique were produced by hot pressing in a laboratory press. The dispersion of SiO2 particles and flax in the composites was studied by scanning electron microscopy (SEM). The related HDPE based composites were subjected to instrumented falling weight impact test. The thermal resistance, stiffness and tensile strength properties of the composites were determined in thermogravimetric analysis (TGA), dynamic-mechanical thermal analysis (DMTA) and tensile tests, respectively. It was found that the impact energy and stiffness value of HDPE/flax composites was markedly higher than that of HDPE but reflect the effects of composite structures and flax content. Incorporation of SiO2 particles enhanced resistance to thermal degradation. It was established that the linear viscoelastic material principle are fairly applicable to convert from the modulus to the creep compliance results. Un- and Modified Polylactide (PLA) /woven Flax Fiber composites Hybrid composites composed of polypropylene (PP) or high-density polyethylene (HDPE), different flax fibers (unidirectional-, biaxial and twill2x2) and silicon dioxide (SiO2) were produced by hot press technique. The ternary polymer composite was effectively fabricated by spraying SiO2 solvents onto the surface of flax fiber. The dispersion of SiO2 particles and flax in the composites was studied by scanning electron microscopy (SEM). The related PP and HDPE based composites were subjected to instrumented falling weight impact test. The thermal and mechanical properties of the composites were determined by thermogravimetric analysis (TGA), dynamic-mechanical thermal analysis (DMTA), creep and stress relaxation tests, respectively. It was found that thermal decomposition temperature of the PP or HDPE/flax composites increased by the addition of SiO2 particles. The impact energy, stiffness, creep resistance and relaxation modulus value of all flax composites increased markedly compared to the PP and HDPE matrix. Time–temperature superposition (TTS) was applied to estimate the creep and relaxation modulus of the composites as a function of time in the form of a master curve. The activation energies for the all PP and HDPE composites systems studied were also calculated by using the Arrhenius equation. The generalized Maxwell model was fairly applicable to the stress relaxation results. Polylactide (PLA)/woven flax fiber textiles/boehmite alumina (BA) composites Composites composed of polylactide (PLA), woven flax fiber textiles (weave style of 2x2 twill and 4x4 hopsack) and boehmite alumina (BA) were produced by hot press. The spraying technique served for the pre-dispersion of the alumina nanoparticles. The aqueous alumina slurry was produced by mixing the water with water dispersible alumina. The dispersion of the flax structures and alumina particles in the composites was studied by scanning electron microscopy (SEM). The PLA composites were subjected to water absorption and instrumented falling weight impact tests. The creep and thermomechanical properties of the composites were determined in short-time creep tests (performed at various temperatures), thermogravimetric analysis (TGA) and dynamic-mechanical thermal analysis (DMTA), respectively. It was found that the incorporation of alumina particles reduced the water uptake compared to the PLA/flax blends. The impact energy and stiffness value of PLA/flax blends was markedly higher than that of PLA but reflected the effects of composite structures. Incorporation of alumina particles enhanced storage modulus and the creep resistance compared to the PLA/flax blends but slightly incremented thermal resistance at high temperature. No clear trend in the flax weave style- effect was found in the thermal behaviour. The creep master curves were constructed by applying the time-temperature superposition (TTS) principle. The Findley power law could satisfactorily describe the creep compliance vs. time traces for all systems studied. Poly(hydroxybutyrate-co-hydroxyvalerate)/sisal natural fiber/clay composites Poly(hydroxybutyrate-co-hydroxyvalerate)(PHBV) biocomposites different sisal containing with the fiber length of 0.25 and 5 mm, and addition of clay particles were prepared by hot compression technique. Silane (Bis(triethoxysilylpropyl)tetrasulfide) treatment has been used to modify in order to enhance the properties of related hybrid composites. The all composites were subject to water absorption test. The mechanical properties of hybrid composites such as tensile stiffness and strength, toughness and hardness determined in tensile, impact and hardness tests, respectively. It was found that tensile strength, stiffness and impact strength of long sisal fiber improved with increasing fiber content. Hardness of short sisal fiber improved with increasing fiber content. Treated Silane of long fibers at 20 wt.% loading was found to enhance the tensile strength fiber by 10% and impact strength by 750% as compared to the neat PHBV. Note that this feature was also confirmed by the appearance of a scanning electron microscopy. Moreover, the hardness and water resistance of the PHBV/sisal composites increased by the addition of clay particles. The diffusion coefficient for the PHBV and hybrid composites systems studied were also calculated. / Bioverbundwerkstoffe aus biologisch abbaubarem Polymer als Matrix und Naturfasern als Verstärkung sind ohne weiteres umweltfreundliche Materialien. Beide Bestandsmaterialien sind vollständig biologisch abbaubar und hinterlassen keine schädlichen Bestandteile auf der Erde zurück. Die als Verstärkung verwendeten Naturfasern wurden aufgrund ihrer Vorteile gegenüber Glasfasern, wie z.B. geringe Kosten, hohe spezifische Festigkeit und Steifigkeit, geringe Dichte, Erneuerbarkeit und Kompostierbarkeit ausgesucht. Der Hauptfokus dieser Arbeit lag darin Naturfasern und/oder Nanopartikel mit Polyethylen (PE), Polypropylen (PP) und Polylactid (PLA) herzustellen, sowie Poly-Hydroxybutyrat-Co-Hydroxyvalerat (PHBV) Matrizen und deren Struktur-Eigenschaft-Verhältnis zu bestimmen. Die folgenden Kurzfassungen der vorliegenden Forschungsarbeit sind vielfältig: BINÄRE VERBUNDWERKSTOFFE Polylactid (PLA)/ Flachsmatten-Verbundwerkstoffe Die Polylactid (PLA)/Flachsmatte und modifizierte PLA/Flachsmatten-Verbundwerkstoffe wurden im Pressverfahren hergestellt. Als Modifikator für das PLA wurden zwei nicht regulierte Wachs/Ethylen-Acrylat-Copolymer/Butyl-Acrylat und Acryl Additive verwendet. Die Verteilung der Flachsmatte in den Verbundwerkstoffen wurde mit dem Rasterelektronenmikroskop (SEM) untersucht. Die PLA-Verbundwerkstoffe wurden dem instrumentalisierten Fallgewichtsschlagzähigkeitstest unterzogen. Die mechanischen und thermischen Eigenschaften der Verbundwerkstoffe wurden im Zugversuch, der thermogravimetrische Analyse (TGA) und der dynamisch mechanischen Thermoanalyse (DMTA) jeweils bestimmt. Es zeigte sich, dass die PLA/Flachsmatten-basierten Verbundwerkstoffe eine erhöhte Schlagzähigkeit aufwiesen. Die Zähigkeitswerte der modifizierten PLA/Flachsmatten-Verbundwerkstoffe waren leicht verringert im Vergleich zum PLA. Die Bruchdehnungswerte zeigten eine Verbesserung der Verformbarkeit des modifizierten PLAs und dessen Verbundwerkstoffe. Nach Zugabe eines Wärme-Modifikators verbesserte sich der Wärmewiderstand auf unter Verarbeitungstemperatur des PLA und hatte nur einen unwesentlichen Einfluss auf die Glasübergangstemperatur des PLA. Die Hauptkurve des Speichermoduls wurde mit der Zeit-Temperatur-Überlagerung (TTS) aufgestellt. Auf alle untersuchten Systeme konnte das dafür gut geeignete Prinzip der linear viskoelastischen Werkstoffe angewendet werden um die Steifigkeit in die Kriechneigung umzuwandeln. Polylactid (PLA)/Flachstextilgewebe-Verbundwerkstoffe Die Polylactid (PLA)/Flachstextilgewebe 2x2 Körper und 4x4 Gewebe mit Leinwandbindung-Verbundwerkstoffe wurden im Intervall-Pressverfahren hergestellt. Das PLA wurde mit zwei Flachsgewebeformen verstärkt. Die Verteilung der Flachs-Verbundwerkstoffstrukturen in den Verbundwerkstoffen wurde mit dem Rasterelektronenmikroskop (SEM) untersucht. Die PLA Verbundwerkstoffe wurden dem instrumentalisierten Fallgewichtsschlagzähigkeitstest unterzogen. Die mechanischen Eigenschaften (Zugfestigkeit, Steifigkeit und Festigkeit) der jeweiligen Verbundwerkstoffe wurden in Zugversuchen und dynamisch mechanischen Thermoanalysen (DMTA) bestimmt. Das Rasterelektronenmikroskop zeigte auf, das der Grenzflächenzwischenraum von rausgezogenen Fasern sich durch das Herstellen im Intervall-Pressverfahren verbessert hat. Auch zeigte sich, dass beide Arten der Flachs-Verbundwerkstoffe die Schlagzähigkeit der Verbundwerkstoffe erhöht im Vergleich zum puren PLA. Die Zugfestigkeit- und Steifigkeitswerte der PLA/Flachs-Verbundwerkstoffe waren deutlich höher als die der puren PLA und spiegeln die Effekte von Verbundwerkstoffstrukturen wieder. Die berechnete Kriechneigung im Speichermodul wurde durch die Anwendung des Zeit-Temperatur-Überlagerung (TTS) Prinzips aufgestellt. Die errechnete Kriechgeschwindigkeit der Flachs-Verbundwerkstoffe war wesentlich geringer als im puren PLA. Polyethylen und Polypropylen/Nanosilikon Dioxid/Flachs-Verbundwerkstoffe Verbundwerkstoffe hergestellt aus Polylactid (PLA), modifiziertem PLA und Flachsfasertextilgewebe (Flachsgewebeform von 2x2 Körper und 4x4 Gewebe mit Leinwandbindung) wurden im Pressverfahren hergestellt. Zwei strukturell unterschiedliche Additive wurden verwendet um das PLA zu modifizieren. Die Verteilung der Flachs-Verbundwerkstoffstruktur wurde unter dem Rasterelektronenmikroskop (SEM) und dem computergestütztes Computer-Tomography-System (µCT) untersucht. Die PLA Verbundwerkstoffe wurden dem Wasseraufnahme- und instrumentalisierten Fallgewichtsschlagzähigkeitstest unterzogen. Die Kriech- und thermomechanischen Eigenschaften der respektiven Verbundwerkstoffe wurden in der thermogravimetrischen Analyse (TGA), der dynamisch mechanischen Thermoanalyse (DMTA) und dem Kurzzeit-Kriechversuch bestimmt. Das modifizierte PLA und dessen Verbundwerkstoffe zeigten eine Erhöhung der Schlagzähigkeit im Vergleich zum unmodifizierten PLA. Die Einbindung von Flachs verringerte den Widerstand gegenüber thermischer Degradierung und erhöhte die Wasseraufnahme. Die Schlagenergie- und Steifigkeitswerte der PLA/Flachs-Verbundwerkstoffe war deutlich höher als die der PLA aber spiegelt die Effekte von Verbundwerkstoffstrukturen mit Flachsinhalt wieder. Die Hauptkurve des Speichermoduls wurde mit dem Zeit-Temperatur-Überlagerung (TTS) Prinzip aufgestellt. Das Datenmaterial der Hauptkurve zeigte den Effekt des modifizierten PLAs auf dem Speichermodul deutlich ausgeprägter im Bereich der Niederfrequenz. Polylactide (PLA)/Flachfasertextilgewebe/Böhmit Aluminumoxid (BA)-Verbundwerkstoffe Die textilen Bioverbundwerkstoffe wurden aus flachsfaserverstärkten Poly(Butylen Adipat-Co-Terephtalat) (PBAT) Gewebe und Vlies im Formpressverfahren mit der Folien-Stapelmethode hergestellt. Die mechanischen Eigenschaften (wie Zugfestigkeit und Steifigkeit, Biegefestigkeit, Steifigkeit und Schlagzähigkeit) der jeweiligen textilen Bioverbundwerkstoffe wurde in Zug-, Biege-, und Schlagtests ermittelt. Die PBAT basierten Verbundwerkstoffe wurden dem Wasseraufnahmetest unterzogen. Der Vergleich der mechanischen Eigenschaften wurde zwischen reinem PBAT und textilen Verbundwerkstoffen durchgeführt. Der Einfluss der Flachsgewebeformen auf die mechanischen Eigenschaften wurde ebenfalls untersucht. Die Ergebnisse zeigten das die Festigkeit der textilen Bioverbundwerkstoffe mit der Webart der Fasern anstieg, signifikant in Bezug auf die Steifigkeit bei einer erhöhten Verdichtung der Fasern. Die 4x4 flachfasergewebten (4-Schussfaden-Windung und 4-Kettfaden-Windung) verstärkten Bioverbundwerkstoffe zeigten die höchste Festigkeit und Steifigkeit im Vergleich zu den anderen textilen Bioverbundwerkstoffen und dem puren PBAT. Dieses Resultat wurde der Beschaffenheit der 4x4-flachfasergewebten Webart zugewiesen. Das Aminopropyltriethoxysilan beeinträchtigte die mechanischen Eigenschaften und Wasseraufnahme der entstandenen Verbundlaminate durch Oberflächenkompatibilität zwischen der Flachsfaser und dem PBAT. HYBRIDE VERBUNDWERKSTOFFE Polyethylen/Nanopartikel, natürliche und tierische Verbundwerkstoffe Binäre und ternäre Verbundwerkstoffe, bestehend aus hoch dichtem Polyethylen (HDPE), Böhmit Aluminumoxid (BA) und verschiedenen natürlichen und tierischen Fasern wie Flachs, Schwammgurke (SG), Palmfaser und Schweinehaar (PH), wurden im Pressverfahren hergestellt. Vorbereitend wurden wasserhaltige BA-Suspensionen auf die HDPE/Flachsmatte gesprüht um nanopartikel/naturfaserverstärkte ternäre Polymer-Verbundwerkstoffe nach dem Trocknen zu erhalten. Die Verteilung der Natur-,Tierfasern und der BA-Partikel in den Verbundwerkstoffen wurde unter dem Rasterelektronenmikroskop untersucht und diskutiert. Die thermomechanischen und Spannungsrelaxation-Eigenschaften der jeweiligen Verbundwerkstoffe wurden in der thermogravimetrischen Analyse (TGA), der dynamisch mechanischen Thermoanalyse (DMTA) und dem Kurzzeit-Stressrelaxationstest (bei unterschiedlichen Temperaturen durchgeführt) bestimmt. Die HDPE-basierten Verbundwerkstoffe wurden Wasseraufnahme- und instrumentalisierten Fallgewichtsschlagzähigkeitstests unterzogen. Es wurde festgestellt, dass alle Verbundwerkstoffsysteme eine Erhöhung der Steifigkeit und Spannungsrelaxation und eine Verminderung der Kerbschlagzähigkeit aufzeigten. Die Spannungsrelaxations-Steifigkeit von Naturfaser-, Tierfaserverbundwerkstoffen war größer im Vergleich zu reinem HDPE. Diese Steifigkeit steig deutlich an mit der Einbindung von BA. Die Hauptkurven der Relaxation wurden mit dem Zeit-Temperatur-Überlagerung (TTS) Prinzip aufgestellt. Die Umkehrung des Findley Potenzgesetzes konnte gut für die Beschreibung der Relaxations-Steifigkeit vs. Zeitüberwachung in allen untersuchten Systemen angewendet werden. Die Einbindung der BA-Partikel erhöhte den Wärmewiderstand, welcher bei höherer Temperatur zu sinken begann im Vergleich zu HDPE/Flachsmatten-Verbundwerkstoff. Der HDPE/Flachsmatte/BA-Verbundwerkstoff konnte die Wasseraufnahme verringern. Polyethylen/Flachs/SiO Verbundwerkstoffe Verbundwerkstoffe bestehend aus hoch dichtem Polyethylen (HDPE), Flachsfasertextilgewebe (Flachsgewebeform 2x2 Körper und 4x4 Gewebe mit Leinwandbindung) und Siliziumdioxid (SiO2) wurden im Pressverfahren mit Nanospritztechnik hergestellt. Die SiO2 Schlämme wurden auf beide Oberflächen des Flachsfasergewebes per Hand gesprüht. Die HDPE/ Flachsfasergewebe-Verbundwerkstoffe wurden in einer Laborpresse im Pressverfahren mit und ohne Nanospritztechnik hergestellt. Die Verteilung der SiO2-Partikel und des Flachs in den Verbundwerkstoffen wurde unter dem Rasterelektronenmikroskop (SEM) untersucht. Die ähnlichen HDPE-basierten Verbundwerkstoffe wurden dem instrumentalisierten Fallgewichtsschlagzähigkeitstest unterzogen. Der Wärmewiderstand, Steifigkeit- und Zugfestigkeit-Eigenschaften der jeweiligen Verbundwerkstoffe wurden in thermogravimetrischen Analysen (TGA), dynamisch mechanischen Thermoanalysen (DMTA) und Zugversuchen bestimmt. Es zeigte sich, dass die Aufprallenergie und Steifigkeitswerte der HDPE/Flachs-Verbundwerkstoffe deutlich höher als die des HDPE waren aber die Effekte von Verbundwerkstoffen mit Flachsinhalt widerspiegeln. Die Einbindung von SiO2-Partikeln erhöhte den Widerstand von thermischer Degradierung. Es wurde bestimmt, das das Prinzip der linear viskoelastischen Werkstoffe gut anwendbar auf die Umwandlung der Steifigkeit zu Kriechneigungsergebnissen ist. Modifizierte und nicht modifizierte Polylactid (PLA)/Flachsfasergewebe-Verbundwerkstoffe Hybride Verbundwerkstoffe aus Polypropylen (PP) oder hoch-dichtem Polyethylen (HDPE), verschiedenen Flachsfasern (unidirektional, biaxial und 2x2 Körper) und Siliziumdioxid (SiO2) wurden im Pressverfahren hergestellt. Der ternäre Polymer-Verbundwerkstoff wurde wirkungsvoll durch das Aufbringen von SiO2 Lösemitteln auf die Oberfläche der Flachsfaser hergestellt. Die Verteilung der SiO2-Partikel und des Flachs in den Verbundwerkstoffen wurde unter dem Rasterelektronenmikroskop (SEM) untersucht. Die ähnlichen PP- und HDPE-basierten Verbundwerkstoffe wurden dem instrumentalisierten Fallgewichtsschlagzähigkeitstest unterzogen. Die thermischen und mechanischen Eigenschaften der respektiven Verbundwerkstoffe wurde in thermogravimetrischen Analysen (TGA), dynamisch mechanischen Thermoanalysen (DMTA), Kriech- und Spannungsrelaxations-Tests bestimmt. Es zeigte sich, dass die thermische Zersetzungstemperatur der PP oder HDPE/Flachs-Verbundwerkstoffe durch das Auftragen der SiO2-Partikel ansteigt. Die Aufprallenergie-, Steifigkeit-, Kriechbeständigkeit- und Relaxation-Steifigkeitn-Werte aller Flachs-Verbundwerkstoffe stiegen deutlich an im Vergleich zur PP und HDPE Matrix. Die Zeit-Temperatur-Überlagerung (TTS) wurde angewandt um die Kriech- und Relaxation-Steifigkeit für die Verbundwerkstoffe als Funktion der Zeit in Form einer Hauptkurve zu schätzen. Die Aktivierungsenergien aller untersuchten PP und HDPE-Verbundwerkstoffsysteme wurden mit der Arrhenius Gleichung errechnet. Das generalisierte Maxwell Model war gut auf die Spannungsrelaxationsergebnisse anwendbar. Polylactide (PLA)/Flachsfasertextilgewebe/Böhmit Aluminiumoxid (BA)-Verbundwerkstoffe Verbundwerkstoffe bestehend aus Polylactid (PLA), Flachfasertextilgewebe (Gewebeform 2x2 Körper und 4x4 Gewebe mit Leinwandbindung) und Böhmit Aluminium (BA) wurden im Pressverfahren hergestellt. Für die Vordispergierung der Aluminiumoxid-Nanopartikel wurde die Spritztechnik angewendet. Die wasserhaltigen Aluminiumoxid-Schlämme wurden durch das Vermischen von Wasser mit wasserdispergierbarem Aluminiumoxid hergestellt. Die Verteilung der Flachsstrukturen und Aluminiumoxid-Partikeln in den Verbundwerkstoffen wurde mit einem Rasterelektronenmikroskop (SEM) untersucht. Die PLA-Verbundwerkstoffe wurden Wasseraufnahme- und instrumentalisierten Fallgewichtsschlagzähigkeitstests unterzogen. Die Kriech- und thermomechanischen Eigenschaften der jeweiligen Verbundwerkstoffe wurden in Kurzzeit-Kriechversuchen (bei unterschiedlichen Temperaturen durchgeführt), thermogravimetrischen Analysen (TGA) und dynamisch mechanischen Thermoanalysen (DMTA) bestimmt. Es zeigte sich, dass das Einbringen der Aluminiumoxid-Partikel die Wasseraufnahme im Vergleich zu PLA/Flachs-Gemischen reduziert. Die Aufprallenergie- und Steifigkeitswerte der PLA/Flachs-Gemische waren signifikant höher als die des PLA aber spiegelten die Effekte von Verbundwerkstoffstrukturen wieder. Das Einbringen von Aluminiumoxid-Partikeln verbesserte die Lagerungs-Steifigkeit und die Kriechbeständigkeit im Vergleich zu PLA/Flachs-Gemischen, erhöhte allerdings leicht den Wärmewiderstand bei hohen Temperaturen. Kein klarer Trend in der Flachswebart konnte dem Temperaturverhalten zugeordnet werden. Die Kriech-Hauptkurven wurden mit dem Zeit-Temperatur-Überlagerung (TTS) Prinzip aufgestellt. Das Findley Potenzgesetz konnte zufriedenstellend die Kriechneigung vs. Zeitüberwachung für alle untersuchten Systeme beschreiben. Poly(Hydroxybutyrat-Co-Hydroxyvalerat)/Natursisalfaser/Ton-Verbundwerkstoffe Poly(Hydroxybutyrat-Co-Hydroxyvalerat) (PHBV) Bioverbundwerkstoffe die Sisalfasern in Längen von 0,25 und 5 mm und Ton-Partikeln enthalten wurden im Heißpressverfahren hergestellt. Die Silan (Bis(Trithoxysilylpropyl)Tetrasulfide) Behandlung wurde für die Modifizierung verwendet um die Eigenschaften von ähnlichen hybriden Verbundwerkstoffen zu verbessern. Alle Verbundwerkstoffe wurden dem Wasseraufnahmetest unterzogen. Die mechanischen Eigenschaften der jeweiligen hybriden Verbundwerkstoffe wie Zugsteifigkeit und Festigkeit, Zähigkeit und Härte wurden in Zugversuchen, Schlagtests und Härteprüfungen bestimmt. Es zeigte sich, dass die Zugfestigkeit, Steifigkeit und Schlagzähigkeit von langen Sisalfasern sich mit der Erhöhung des Fasergehalts verbessert. Behandeltes Silan von langen Fasern mit 20 wt.% Belastung zeigte eine Verbesserung der Faser-Zugfestigkeit um 10% und Schlagzähigkeit von 750% im Vergleich zu reinem PHBV. Diese Besonderheit wurde auch von einem Rasterelektronenmikroskop bestätigt. Weiterhin ist die Härte und Wasserbeständigkeit in PHBV/Sisal-Verbundwerkstoffen durch das Einbringen von Ton-Partikeln angestiegen. Die Diffusionskoeffizienten für die untersuchten PHBV- und hybriden Verbundwerkstoffsysteme wurden auch errechnet.

The main thrust of this thesis is the development of facile synthetic routes for simple boryl anilines and study their structure-property correlations in both solid and solution states and to utilize this information to design functional materials with desired properties such as aggregation induced emission, mechanofluorochromism, and thiol sensors. This thesis contains eight chapters and the contents of each chapter are described below. Chapter 1 The first chapter is an introduction to the theme of the thesis and presents a general review on the present work with emphasis on photophysics of triarylboron based donor-acceptor systems and their applications in various fields. In addition, advances in boron chemistry in the new frontier areas such as aggregation induced emission and mechanochromism are discussed in brief. Chapter 2 The second chapter deals with the general experimental techniques and synthetic procedures utilized in this work. Chapter 3 This chapter describes the rational design and synthesis of triarylborane bearing Unsubstituted amines, namely borylanilines (3.1-3.5). Compounds 3.1-3.4have similar donor and acceptor centres but differ their molecular conformations and also differ in the relative positions of amine moiety (para and meta). Compounds 3.1-3.4 contain one amine group while 3.5 contains two amine moieties. These compounds exhibit fascinating electrostatic intermolecular interactions, N −H- - -π in the crystal structure of 3.1, 3.2 and 3.4 and N −H--N interactions in crystal structure of 3.5. The solution state optical properties of 3.1-3.5 are typical of donor-acceptor (D-A) systems. Interestingly, compounds 3.3 and 3.5 showed unprecedented mechanochromic luminescent properties. Upon grinding, compound 3.3 showed color changes from blue to cyan blue and 3.5 showed intriguing color changes from blue to green and these color changes were found to be reversible. Single crystal X-ray diffraction analysis of 3.5BP (blue emission color crystal) and 3.5GP (green emission color crystal) clearly show that the color changes are due to the difference in their solid state packing. Chapter 4 In chapter 4, the design and facile synthesis of boron based donor-acceptor (D-A) systems such as borylanilines 4.4-4.9 (D= -NH2 for 4.4-4.6 and -NMe2 for compounds 4.7-4.9) are reported. Compounds 4.4, 4.5 and 4.6 contain one, two or three -NH2 moiety(ies), respectively. Compounds 4.7, 4.8 and 4.9 contain one, two or three –NMe2 moiety(ies), respectively. A systematic investigation has been carried out to rationalize the effect of donor-acceptor ratio on the ICT process in borylanilines 4.4-4.9. The aryl spacer between donor amine and acceptor boron is kept the same in all the compounds to avoid the electronic effect of spacer on the ICT characteristics of these compounds. In the case of compounds 4.4-4.6, the increase in the number of donor -NH2 moieties does not affect their absorption profile, while in the case of compounds 4.7-4.9, the absorption spectra are shifted bathochromically with an increase in the number of donor-NMe2 moieties. Photoluminescence (PL) of 4.4-4.6 is significantly blue shifted with an increase in number of –NH2 moieties, while the PL of 4.7-4.9 was slightly blue shifted. The absorption and PL features of 4.4-4.6 are sensitive to the polarity of the solvent medium. In contrast, absorption profiles of 4.7-4.9 are not sensitive to the polarity of the solvent medium. The PL of these compounds is affected by the polarity of the solvent medium. Chapter 5 This chapter deals with triarylboron based fluorescent probes (5.1-5.4) for the selective detection of thiophenols over aliphatic thiols. The probes were constructed by conjugating luminescent borylanilinies with luminescent quencher 2,4-dinitrobenzene sulfonyl (DNBS) moiety. In compound 5.1 and 5.2 the DNBS moiety is positioned at the para position with respect to the triarylborane moiety, while in 5.3 and 5.4 the DNBS moiety(ies) is(are) at the meta position(s). Probes 5.1-5.4 showed selective turn-on fluorescence response towards thiophenol. The fluorescence “off-on” switching mechanism of 5.1-5.4 against thiophenols was fully elucidated by theoretical calculations. Probes 5.1-5.4 are also capable of detecting thiophenols in the intra cellular environments. Chapter 6 Design, facile synthesis and aggregation induced emission properties of a new series of novel triarylboron tethered N-aryl-1,8-naphthalimides (TAB-NPIs) 6.1-6.7 are described in this chapter. Systematic structural perturbation has been used for fine-tuning the optical and morphological properties of TAB- NPIs in both solid as well as in aggregated state. Compounds 6.1-6.7 are weekly luminescent in solutions. In contrast, all compounds (except compound 6.4) are strongly luminescent in the solid state and aggregated state in THF-H2O mixtures. The presence of sterically hindered boryl unit in 6.1-6.7 has endowed these molecules with unique AIE characteristics by preventing co-facial arrangements of NPI moieties. The propeller shape arrangement of TAB moiety in 6.1, 6.2, 6.5, 6.6 and 6.7 effectively prevents the aggregation induced emission quenching (AIEQ) and induce strong emission in the condensed state. In the solid state, compounds 6.1, 6.4, 6.5, and 6.6 generate an interesting supramolecular structure via intermolecular C-H--- and C-H---O interactions. No face to face intermolecular π---π interactions were found in the crystal structures of 6.1, 6.4, 6.5, and 6.6. This precludes the excimer formation which can be detrimental to the radiative process in these molecules. The scanning electron microscopy (SEM) images of as prepared samples of 6.1-6.7 clearly indicate that the morphology of these compounds strongly depends on the molecular conformations and number of naphthalimide moieties in the TAB-NPI conjugates. Chapter 7 This chapter deals with design, synthesis and optical properties of novel dimesitylboryl appended perylenediimides. A simple synthetic strategy has been developed for the construction of novel TAB-PDIs conjugates. These conjugates can be conveniently synthesised by condensation of boryl anilines with perylene tetracarboxylic acid anhydride. The incorporation of TAB moiety enhanced the solubility of perylen bisimides in common organic solvents. The PL quantum yield of both 7.1 and 7.2 strongly depends on the excitation wavelength. Lower Pl efficiency observed for 7.1 and 7.2 upon excitation in the boryl dominated absorption region may be due to the photon induced electron transfer form mesityl units of boryl to perylene bisimide moiety. The morphology as well as emission colours of supramolecular architectures of both 7.1 and 7.2 can be modulated by controlling the concentrations of DCM solutions of these compounds. Both the compounds showed selective fluorogenic response for F-1 and CN-1 anions. The simple synthetic strategy reported in this chapter can be conveniently exploited for the construction of TAB conjugates of semiconducting organic anhydrides. Chapter 8 Novel planar chiral Lewis acids 8.3(SP, SS), 1-phosphino-2-borylferrocenes 8.4(SP) and 2-phosphino-1-borylferrocenes 8.4(RP) have been synthesized from a readily accessible ferrocene sulphinate precursor. Adopting a simple synthetic approach and a single precursor, enantiomerically pure SP and RP isomers have been prepared. It would be worthwhile to investigate the catalytic properties of compounds 8.3(SS), 8.4(SP) and 8.4(RP). It would also be interesting to replace the mesityl groups on boron with other electron deficient groups like pentafluorophenyl and 1,3,5-trifluoromethylphenyl to fine tune the Lewis acidity of boron center and to set-up a general route to enantiomerically pure Planar Chiral Frustrated Lewis Pairs (PCFLP’s).

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第20394号 / 工博第4331号 / 新制||工||1671(附属図書館) / 京都大学大学院工学研究科物質エネルギー化学専攻 / (主査)教授 村田 靖次郎, 教授 辻 康之, 教授 中村 正治 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM

No description available.

In this study, we quantified the Chemistry-Process-Structure-Property (CPSP) relations of a Ti-6Al-4V/TiB functionally graded material to assess its ability to withstand large deformations in a high throughput manner. The functionally graded Ti-6Al-4V/TiB alloy was created by using a Laser Engineered Net Shaping (LENS) process. A complex thermal history arose during the LENS process and thus induced a multiscale hierarchy of structures that in turn affected the mechanical properties. Here, we quantified the functionally graded chemical composition; functionally graded TiB particle size, number density, nearest neighbor distance, and particle fraction; grain size gradient; porosity gradient. In concert with these multiscale structures, we quantified the associated functionally graded elastic moduli and overall stress-strain behavior of eight materials with differing amounts of titanium, vanadium, aluminum, and boron with just one experiment under compression using digital image correlation techniques. We then corroborated our experimental stress behavior with independent hardening experiments. This paper joins not only the Process-Structure-Property (PSP) relations, but couples the different chemistries in an efficient manner to effectively create the CPSP relationships for analyzing titanium, aluminum, vanadium, and boron together. Since this methodology admits the CPSP coupling, the development of new alloys can be solved by using an inverse method. Finally, this experimental data now lays down the gauntlet for modeling the sequential CPSP relationships.

This research is focused on the investigation of phase morphology and blend stability within ionomeric perfluorocyclobutane (PFCB)/poly(vinylidene difluoride) (PVDF) copolymer blend membranes. The morphologies of these unique materials, designed as proton exchange membranes (PEMs) for proton exchange membrane fuel cells (PEMFCs), have been examined not only in the as-cast/as-received state, but also as a function of exposure to various ex-situ aging environments. The morphological investigations used to probe the response of these ionomer blends have been designed to mimic the environment within a PEMFC and will therefore enhance our understanding of the implications of morphological changes which may occur during fuel cell operation. Thermal annealing of the membranes has been conducted to determine the materials' morphological response to various temperatures in the absence of hydration. The results of these thermal annealing studies have facilitated the isolation of morphological contributions stemming from thermal exposure. Immersion of the blend membranes in liquid water has allowed for singular identification of the role of hydration in the blend membranes' morphological rearrangement and phase stability. However, as the typical fuel cell environment to which these membranes will be exposed is complicated by the presence of both temperature and humidity, our ex-situ investigations have also included the exposure of PFCB/PVDF copolymer blend membranes to simultaneous thermal annealing and hydration conditions – a treatment we refer to as "hygrothermal aging." This unique procedure serves as a simplified method whereby the complex fuel cell environment may be simulated, and the resultant morphological response researched. While the work presented herein has enhanced our understanding of the blend stability of the specific membranes investigated, we have also advanced the fundamental knowledge of the role of morphology with respect to the fuel cell performance of blend materials and the corresponding implications of morphological rearrangements. Such an understanding is essential in the development of morphology-property relationships and eventual optimization of membrane materials designed for use in fuel cells. / Ph. D.

No description available.

The component-level performance of materials is fundamentally determined by the underlying microstructural features. Therefore, designing high-performance materials using multi-scale models plays a significant role to improve the predictability, reliability, proper functioning, and longevity of components for a wide range of applications in the fields of aerospace, electronics, energy, and structural engineering. This thesis aims to develop new methodologies to design microstructures under inherent material uncertainty by incorporating machine learning techniques. To achieve this objective, the study addresses gradient-based and machine learning-driven design optimization methods to enhance homogenized linear and non-linear properties of polycrystalline microstructures. However, variations arising from the thermo-mechanical processing of materials affect microstructural features and properties by propagating over multiple length scales. To quantify this inherent microstructural uncertainty, this study introduces a linear programming-based analytical method. When this analytical uncertainty quantification formulation is not applicable (e.g., uncertainty propagation on non-linear properties), a machine learning-based inverse design approach is presented to quantify the microstructural uncertainty. Example design problems are discussed for different polycrystalline systems (e.g., Titanium, Aluminium, and Galfenol). Though conventional machine learning performs well when used for designing microstructures or modeling material properties, its predictions may still fail to satisfy design constraints associated with the physics of the system. Therefore, the physics-informed neural network (PINN) is developed to incorporate problem physics in the machine learning formulation. In this study, a PINN model is built and integrated into materials design to study the deformation processes of Copper and a Titanium-Aluminum alloy. / Doctor of Philosophy / Microstructure-sensitive design is a high-throughput computational approach for materials design, where material performance is improved through the control and design of microstructures. It enhances component performance and, subsequently, the overall system's performance at the application level. This thesis aims to design microstructures for polycrystalline materials such as Galfenol, Titanium-Aluminum alloys, and Copper to obtain desired mechanical properties for certain applications. The advantage of the microstructure-sensitive design approach is that multiple microstructures can be suggested, which provide a similar value of the design parameters. Therefore, manufacturers can follow any of these microstructure designs to fabricate the materials with the desired properties. Moreover, the microstructure uncertainty arising from the variations in thermo-mechanical processing and measurement of the experimental data is quantified. It is necessary to address the resultant randomness of the microstructure because it can alter the expected mechanical properties. To check the manufacturability of proposed microstructure designs, a physics-informed machine learning model is developed to build a relation between the process, microstructure, and material properties. This model can be used to solve the process design problem to identify the processing parameters to achieve a given/desired microstructure.