The master's thesis focuses on preparation of blown films from polylactid acid (PLA) which was blended with selected polyesteres – poly(butylene adipate-co-terephtalate) (PBAT), polycaprolactone (PCL) and polybutylene succinate (PBS) – and thermoplastic starch (TPS) in amount of 30% in order to soften PLA films. The influence of the aditives on static and mechanical tensile properties, on structure, morphology and thermal properties of the films was determined and the obtained parameters were compared to properties of films prepared from neat PLA and high density polyethylene (HDPE). The results showed that the additives increased crystalinity of PLA and thus significantly influenced the properties of the films. In contrast to the film from neat PLA, softening in terms of lowering glass transition temperature occured only by adding PBS and TPS, in terms of increasing ductility only by adding PBAT. All PLA films showed nearly constant elastic modulus up to the beginning of glass transition enabling their potential application till 50 °C. Preparation of the film with TPS was problematic and the film showed the worst mechanical properties. Preparation of other films was without any problems. The most promising additive from the tested ones was PBAT which showed comparable mechanical properties as the film from HDPE.

In der vorliegenden Dissertationsarbeit wird auf die Thematik der Entwicklung von Polymerwerkstoffen, basierend auf vollständig natürlichen Resourcen, eingegangen. Die vorliegende Lösung beruht auf der Compoundierung von Polylactid mit unterschiedlich modifizierten Vanillin. Ziel war es, flammschutzwirkende Komponenten einzubringen und die Abhängigkeiten zwischen Zusammensetzung und Eigenschaften aufzuklären. Dem liegt die Absicht zugrunde, optimale Werkstoffe zur Verfügung zu stellen, die sich durch deutlich verbesserte flammhemmende und mechanische bzw. thermo-mechanische Eigenschaften auszeichnen. Die erzeugten modifizierten Vanillin-Derivate sowie deren Composite wurden hinsichtlich der physikalischen und chemischen Struktur mittels REM, EDX, FTIR, NMR, DSC, TGA, SEC und Zugversuch charakterisiert. Zur Bestimmung der flammwidrigen Eigenschaften wurden UL-94 V, LOI und CCT durchgeführt. Es hat sich gezeigt, dass System aus PLA und einem Vanillin-Phosphorsäure-Ester in Bezug auf werkstofflichen Eigenschaften insgesamt die optimale Leistung aufwies. Die Materialen ergaben eine verbesserte Zähigkeit und erheblich erhöht flammwidrige Eigenschaften. In einem weiteren Schritt wurden MMT und APP, zwei kommerzielle Flammschutzmittel, mit dem PLA/VP System kombiniert. Die daraus abgeleiteten Resultate bewiesen eine synergistische Wirkung zwischen VP und MMT bzw. APP und führten zu besseren Brandklassen bei LOI und UL-94 Brandtests. / The present work demonstrates the development of fully bio-based polymeric composites. It was realized by the compounding of poly(lactic acid) and differently modified vanillin. The aim of this work was to introduce flame retardant components into PLA and to study the flame retardant mechanism. The intention of this approach is the preparation of optimized PLA composites with significantly improved flame retardant, mechanical as well as thermo-mechanical properties. The modified vanillin and the PLA composites based on those vanillin derivatives were characterized by means of SEM, EDX, FTIR, NMR, DSC, TGA, SEC and tensile test for their physical and chemical structures. UL-94 V, LOI and CCT were carried out to determine the corresponding flame retardant properties. The results showed that, the PLA/VP system represented the best overall performance. The PLA/VP composite exhibited increased toughness and significantly improved flame retardancy. In addition, two commercialized flame retardants, MMT and APP, were introduced into the PLA/VP system, respectively. It was suggested that there were synergic effects between VP and MMT as well as APP. The combined used flame retardants resulted in an improved classification in UL-94 and LOI tests.

Les assemblages colloïdaux représentent une nouvelle piste très prometteuse dans le domaine de l'ingénierie tissulaire. Idéalement, ce type d'assemblage permet l'obtention de matériaux injectables et gélifiants sur le site lésionnel, favorisant par la suite le développement de néo-tissus viables. Ce travail porte sur la formation de tels assemblages à base de chitosane et de poly(acide lactique) (PLA). Deux types d'assemblages ont été conçus et étudiés dans ce travail. Dans une première approche, le mélange de particules anioniques de poly (acide lactique) (PLA) avec du chitosane en solution faiblement acide conduit à la formation de « gels composites », résultant des interactions colloïde-polymère. Des analyses rhéologiques et de diffusion des rayons X aux petits angles ont permit de mettre en évidence le mode de formation et l'influence de plusieurs paramètres sur les propriétés finales de ces gels. Notamment, ils présentent des propriétés rhéofluidifiantes et un caractère réversible, c'est-à-dire que le gel peut se reformer après déstructuration mécanique. Le second type d'assemblage résulte du mélange de particules anioniques de PLA et de nanogels cationiques de chitosane, conduisant à la formation de « gels colloïdaux », par interactions colloïde-colloïde. L'influence de plusieurs facteurs sur la formation et les propriétés de ces gels a également été étudiée par mesures rhéologiques. Notre étude s'est notamment orientée sur la caractérisation et la stabilité des hydrogels physiques de chitosane sous forme colloïdale, ainsi que sur l'optimisation de leur cohésion / Colloidal assemblies may be a promising pathway to obtain injectable scaffolds favoring the development of neo-tissue in regenerative medicine. This work investigates the formation of such assemblies composed of chitosan, soluble or in suspension (nano-hydrogel), and poly(lactic acid) (PLA) nanoparticles. Two types of assemblies are studied. As a first approach, mixing negatively charged PLA particles and chitosan solution leads to the formation of “composite gels”, based on colloidpolymer interactions. Rheological and Small Angle X-Ray Scattering measurements highlighted the formation process and the influence of various parameters on final properties of these gels, which features shear-thinning and reversibility behavior, that is, the capacity to gel again after yielding. PLA nanoparticles could also be mixed with cationic chitosan nanoparticles, which are crosslinker free nano-hydrogels, leading to the formation of “colloidal gels”, based on colloid-colloid interactions. Influence of various parameters on gel synthesis and properties are investigated through rheological measurements. The study also focuses on the characterization and control of the morphological and cohesion properties of chitosan nanogel

Cette étude est une contribution à la valorisation du grignon d’olives (GO), sous produits oléicoles à caractère lignocellulosique. La voie proposée consiste à utiliser le GO comme charge dans des polymères de grande diffusion à savoir le poly (éthylène/propylène) [CEP] d’origine fossile et le poly (acide lactique) [PLA], issu des ressources renouvelables. Les différentes formulations, CEP/GO et PLA/GO, élaborées à l’état fondu dans une extrudeuse bivis ont été étudiés du point de vue des propriétés rhéologiques, thermique, mécanique et de la morphologie. Différents tiers-corps copolymères de structures diverses ont été utilisés dans le but de promouvoir l’adhésion à l’interface des composants et/ou de réduire la dégradation du polymère matrice et améliorer les performances des systèmes composites ainsi conçus. Les observations morphologiques ont corroboré parfaitement l’ensemble des propriétés étudiées. / This study is a contribution to the valorization of Olive Solid Waste (OSW) which displays a Lignocellulosic nature. The proposed approach consists in using the OSW as a filler in commodity polymers namely the poly (ethylene/propylene) [CEP] of fossil origin and the poly (lactic acid), derived from renewable resources. The different formulations, CEP/GO and PLA/GO, processed in the molten state in a twin screw extruder were studied from the side of rheological, thermal, mechanical properties and morphology. Different copolymers of various structures were used in order to promote the adhesion in the interface of the components and/or to reduce the polymer matrix degradation and to improve the composite systems performances. Morphological observations corroborated perfectly the studied properties.

Tesis por compendio / [ES] En esta tesis se obtuvieron fracciones celulósicas y extractos activos de paja de arroz mediante diferentes técnicas de extracción y purificación, utilizando agua como disolvente. Estas fracciones se incorporaron en películas de almidón y PLA, y en bicapas de almidón-PLA, para obtener materiales de envasado activos para extender la vida útil de diferentes alimentos. Los extractos obtenidos por combinación de ultrasonidos y calentamiento a reflujo (USHT) y con agua subcrítica (SWE) (a 160 °C (SWE-160) y 180 °C (SWE-180)) presentaron un alto contenido fenólico (37, 51 y 83 mg GAE.g-1 de extracto seco, respectivamente) y actividad antioxidante (6,3, 2,0 y 1,2 mg de extracto seco.mg-1 DPPH, respectivamente). Los extractos SWE fueron activos contra L. innocua y E. coli. Se aislaron fibras de celulosa (FC) del residuo insoluble de las diferentes extracciones. A pesar de las ligeras diferencias en el grado de purificación, los nuevos métodos dieron lugar a FCs con rendimientos más elevados que el método alcalino (35-39 % frente al 29 %), con cristalinidad (60-69 %), comportamiento térmico y relación de aspecto (20-60) similares. Se incorporaron fibras USHT al 1, 3 y 5 % (p/p) en películas termoprocesadas de almidón de maíz, y de almidón de maíz modificado térmicamente. La incorporación al 3 % dio lugar a películas con mejores propiedades funcionales. Los extractos activos (al 4, 6 y 8 % en peso) en la matriz de almidón, con o sin CF (3 %), dieron lugar a películas más extensibles y menos resistentes, con mayor capacidad de barrera al oxígeno. Las bolsas monodosis de aceite de girasol con estas películas activas y reforzadas redujeron eficazmente la oxidación. Las películas activas de PLA termoprocesado, con diferentes proporciones (2, 4 y 6 % p/p) del extracto USHT, presentaron color y propiedades mecánicas ligeramente peores, pero con mayor barrera al oxígeno. La cinética de liberación de los antioxidantes incorporados en simulantes alimentarios de diferente polaridad (A: productos acuosos; y D1: sistemas de aceite en agua), mostró que las películas con un 6% de extracto, tuvieron una capacidad antioxidante similar en simulantes con distinta polaridad. Se obtuvieron bicapas biodegradables laminando PLA, con y sin extracto USHT (6 %), y almidón termoplástico, con o sin FC USHT (3 %). Las bicapas mostraron mejor capacidad de barrera global que las monocapas. Sin embargo, la migración de compuestos entre capas dio lugar a películas menos rígidas y resistentes de lo esperado de la contribución del film de PLA. Las bicapas activas y reforzadas alargaron la vida útil de carne de cerdo refrigerada. Las películas de PLA con un 6 % (p/p) de los diferentes extractos (USHT, SWE-160 y SWE-180) presentaron menor resistencia mecánica y capacidad de barrera al vapor de agua, pero una mayor capacidad de barrera al oxígeno y a la luz UV. Además, estas películas, especialmente con el extracto SWE-180, alargaron la vida útil de la carne de cerdo refrigerada. Las FCs obtenidas con los diferentes métodos de purificación también se utilizaron para producir aerogeles de celulosa. Las diferencias composicionales afectaron a la microestructura de los aerogeles. La capacidad de absorción y de retención de agua de los aerogeles estuvo dentro de los rangos descritos para este tipo de materiales. Por tanto, fue posible obtener fracciones valorizadas de la paja de arroz, extractos activos y fibras celulósicas, útiles en el desarrollo de materiales biodegradables activos a base de almidón y PLA. Son necesarios más estudios para validar la seguridad alimentaria de los materiales, así como para el desarrollo de otras aplicaciones en el campo de la industria alimentaria o farmacéutica. / [CA] En aquesta tesi doctoral es van obtenir fraccions cel·lulòsiques i extractes actius de palla d' arròs mitjançant l'aplicació de diferents tècniques d'extracció i purificació, utilitzant aigua com a dissolvent. Aquestes fraccions es van incorporar a pel·lícules de midó i PLA, i bicapes de midó-PLA, per obtenir materials d'envasament actius útils per allargar la vida útil de diferents aliments. Els extractes combinant ultrasons i escalfament a reflux (USHT) i amb aigua subcrítica (SWE) (a 160 °C (SWE-160) i 180 °C (SWE-180)) van mostrar un alt contingut fenòlic (37, 51 i 83 mg GAE.g-1 d'extracte sec, respectivament) i activitat antioxidant (6,3, 2,0 i 1,2 mg d'extracte sec.mg-1 DPPH, respectivament). Els extractes SWE van mostrar activitat antibacteriana contra L. innocua i E. coli. Es van aïllar fibres de cel·lulosa (FC) de les fraccions insolubles de l'extracció. Malgrat les lleugeres diferències en el grau de purificació, els nous mètodes van donar lloc a FCs amb rendiments més elevats que el mètode alcalí (35-39 % enfront del 29 %), amb cristal·linitat (60-69 %), comportament tèrmic i relació d'aspecte (20-60) similars. Es van incorporar fibres USHT a l'1, 3 i 5 % (p/p) en pel·lícules de midó de dacsa, i de midó de dacsa modificat per tractament tèrmic. La incorporació al 3 % va donar lloc a pel·lícules amb les millors propietats funcionals. Els extractes actius (al 4, 6 i 8 % en pes) a la matriu de midó, amb o sense CF (3 %), proporcionaren pel·lícules més extensibles i menys resistents, però amb més capacitat de barrera a l'oxigen. Les bosses monodosi de l'oli de gira-sol amb aquestes pel·lícules actives i reforçades van reduir eficaçment l'oxidació. Les pel·lícules actives de PLA amb diferents proporcions (2, 4 i 6 % p/p) de l'extracte USHT, presentaren color i propietats mecániques lleugerament pitjors, però amb major capacitat de barrera a l'oxigen. La cinètica d'alliberament dels antioxidants incorporats, en simulants alimentaris de diferent polaritat (A: productes aquosos; i D1: sistemes d'oli en aigua), va mostrar que les pel·lícules amb un 6% d'extracte, tenien una capacitat antioxidant similar en simulants amb diferent polaritat. Es van obtenir bicapes biodegradables laminant PLA, amb i sense extracte USHT (6 %), i midó termoplàstic, amb o sense FC USHT (3 %). Les bicapes van mostrar millor capacitat de barrera global que les monocapes. No obstant això, la migració de compostos entre capes va donar lloc a pel·lícules menys rígides i resistents respecte a l'esperat de la contribució de la pel·lícula de PLA. Les bicapes actives i reforçades van allargar la vida útil de carn de porc refrigerada. Les pel·lícules de PLA amb un 6 % (p/p) dels diferents extractes (USHT, SWE-160 i SWE-180) van presentar menor resistència mecànica i capacitat de barrera al vapor d'aigua, però una major capacitat de barrera a l'oxigen i a la llum UV. A més, aquestes pel·lícules, especialment amb l'extracte SWE-180, van allargar la vida útil de la carn de porc refrigerada. Les FCs obtingudes amb els diferents mètodes de purificació també es van utilitzar per produir aerogels de cel·lulosa. Les diferències composicionals van afectar la microestructura dels aerogels. La capacitat d' absorció i de retenció d'aigua dels aerogels va estar dins dels rangs descrits per a aquest tipus de materials. Per tant, va ser possible obtenir fraccions valoritzades de la palla d' arròs, extractes actius i fibres cel·lulòsiques, útils en el desenvolupament de materials biodegradables actius a base de midó i PLA. Són necessaris més estudis per validar la seguretat alimentària dels materials, així com per al desenvolupament d' altres aplicacions en el camp de la indústria alimentària o farmacèutica. / [EN] This Doctoral thesis focused on obtaining cellulosic fractions and bioactive extracts from rice straw (RS) by applying different extraction and purification techniques, using water as a green solvent. These fractions were incorporated into starch and poly (lactic acid) (PLA)-based films, as well as into starch-PLA bilayers, to obtain active packaging materials useful for extending the shelf life of different food matrices. The extracts obtained by applying a combined ultrasound-reflux heating method (USHT) and subcritical water extraction (SWE) (at 160 °C (SWE-160) and 180 °C (SWE-180)) exhibited high phenolic content (37, 51, 83 mg GAE.g-1 dry extract, respectively) and antioxidant activity (6.3, 2.0, and 1.2 mg dry extract.mg-1 DPPH, respectively). The SWE extracts showed antibacterial activity against L. innocua and E. coli. Cellulose fibres (CF) were isolated from the extraction insoluble fractions and compared with those obtained from the traditional alkaline method. Despite slight differences in the degree of purification, the new methods gave rise to CFs with higher yields than the alkaline method (35-39% vs. 29%), with similar crystallinity (60-69%), thermal behaviour, and aspect ratios. USHT fibres were incorporated into corn starch (1, 3, and 5% wt.), and corn starch-modified by heat treatment, obtained by thermoprocessing. The incorporation of CF at 3% gave rise to films with the best functional properties. When active extracts were incorporated at different ratios (4, 6, and 8% wt.) into the starch matrix, with or without CF (3%), the films were more stretchable and less resistant, but with higher oxygen barrier capacity. Likewise, mono-dose bags of these active and reinforced films effectively reduced the oxidation of packed sunflower oil. Active, plasticised PLA films were produced, incorporating USHT extract (2, 4, and 6% wt.) by thermoprocessing, which exhibited colour and slightly worsened tensile behaviour, but with higher oxygen barrier capacity. The release kinetics of the incorporated antioxidant compounds in food simulants of different polarity (A: aqueous products; and D1: oil-in-water systems) showed that films containing 6% of extract delivered similar antioxidant capacity regardless of the food simulant polarity. Biodegradable bilayers were obtained by laminating plasticised PLA, with and without USHT extract (6%), and thermoplastic starch, with or without USHT CFs (3%). The bilayers exhibited improved overall barrier capacity with respect to the monolayers. However, the interlayer compound migration led to less stiff and resistant films with respect to that expected from the PLA film contribution. The active and reinforced bilayers were able to extend the shelf life of the packed pork meat during cold storage. PLA films with 6% wt. of the different extracts (USHT, SWE-160, and SWE-180) were produced, which exhibited lower mechanical resistance and water vapour barrier capacity, but improved oxygen barrier capacity and intense UV light-blocking effect. Furthermore, the active PLA films, especially with SWE-180 extract, extended the shelf life of cold storage pork meat. The CFs obtained with the different purification methods were also used to produce cellulose aerogels. The differences in the chemical composition of the CFs affected the aerogels' microstructure. The water absorption and retention capacity of the aerogels were within the previously reported ranges for this type of material. Thus, it was possible to obtain valorised fractions of rice straw, active extracts and cellulosic fibres, useful in developing active biodegradable materials based on starch and PLA. Further studies are needed to validate the food safety of the materials, as well as for developing other applications in the food or pharmaceutical industry. / The authors thank the Agencia Estatal de Investigación (Spain) for the financial support through projects PID2019-105207RB-I00/AEI/10.13039/501100011033 and Generalitat Valenciana [grant number GrisoliaP/2019/115]. / Vieira De Freitas, PA. (2022). Valorisation of rice straw by obtaining active compounds and cellulosic materials for the development of biodegradable food packaging systems [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/191380 / Compendio

La vaccination est l’un des moyens les plus efficaces de la médecine moderne dans le combat contre les maladies infectieuses. L’amélioration de l’efficacité des vaccins requiert la mise au point d’adjuvants permettant d’accroître la qualité de la réponse immunitaire. À titre d’exemple, les nanoparticules (NP) de poly(acide lactique) (PLA) constituent un système efficace pour la délivrance d’antigènes. Afin de renforcer leur potentiel vaccinal, ce travail de recherche a eu pour objectif d’élaborer des NP de PLA décorées en surface par des molécules immunostimulantes, le D-mannose ou un peptide dérivé de l’interleukine-Beta, et au cœur, par l’imiquimod. Notre stratégie repose sur l’utilisation d’un tensioactif macromoléculaire composé d’un bloc de PLA et d’un bloc de poly(N-acryloxysuccinimide-co-N-vinylpyrrolidone) (P(NAS-co-NVP)), dont les fonctions ester de N-succinimidyle (NS) permettent le couplage de biomolécules. Ce copolymère a été synthétisé par combinaison de la polymérisation par ouverture de cycle et de la polymérisation radicalaire contrôlée par les nitroxydes (NMP). Après l’étude de la copolymérisation du NAS et de la NVP par NMP à partir d’une alcoxyamine modèle (MAMA-SG1), leur copolymérisation a été réalisée à partir de la macro-alcoxyamine PLA-SG1, conduisant au copolymère PLA-b-P(NAS-co-NVP) désiré. Des NP de PLA ont alors été préparées par nanoprécipitation et diafiltration en présence du copolymère, conduisant à des tailles respectives de 150 et 500 nm. Des études de potentiel zêta et de spectrométrie UV ont démontré la présence des esters de NS à la surface des NP (2.4 fonctions.nm-2), disponibles pour le couplage des biomolécules. Des micelles de copolymère ont été également préparées, après substitution des esters de NS par des sucres, et permettent une encapsulation efficace de l’imiquimod, contrairement aux NP de PLA. Ces systèmes constituent une plateforme flexible d’adjuvants potentiels comme alternative aux adjuvants non biodégradables actuellement utilisés. / Vaccination represents one of the most powerful tools of medicine for the fight against infectious diseases. The improvement of vaccine efficiency needs the development of adjuvants able to increase the quality of the immune response. Poly(lactic acid) (PLA) nanoparticles (NPs) represent an efficient system for antigen delivery. In order to improve their vaccine potential, the goal of this research work was to elaborate PLA NPs decorated at the surface with immunostimulatory molecules, D-mannose or peptide derived from interleukine-Beta, and into the core with imiquimod. Our strategy relies on the use of a macromolecular surfactant composed of a PLA block and a poly(N- acryloxysuccinimide-co-N-vinylpyrrolidone) (P(NAS-co-NVP)) block, whose N-succinimidyl (NS) activated esters allow the coupling of biomolecules. This diblock copolymer was synthesized by the combination of ring opening polymerization and nitroxide mediated polymerization (NMP). After the study of the copolymerization of NAS and NVP by NMP from the MAMA-SG1 model alkoxyamine, their copolymerization was performed from the macro-alkoxyamine PLA-SG1, leading to the desired copolymer PLA-b-P(NAS-co-NVP). PLA NPs were then prepared by nanoprecipitation and diafiltration, in the presence of the copolymer, leading to 150 nm and 500 nm sized particles, respectively. Studies of zeta potential and UV spectrometry demonstrated the presence of NS-activated esters at the NP surface (2.4 functions.nm-2), available for the coupling of biomolecules. Micelles from copolymer were also prepared, after substitution of esters with carbohydrates, and allowed an efficient encapsulation of imiquimod, contrary to PLA NPs. These systems represent a flexible platform of potential adjuvants as an alternative to non-biodegradable adjuvants currently used.

The relatively new and still growing field of 3D-printing has opened up the possibilities to manufacture patient-specific medical devices with high geometrical accuracy in a precise and quick manner. Additionally, biocompatible materials are a demand for all medical applications while biodegradability is of importance when developing scaffolds for tissue growth for instance. With respect to this, this project consisted of developing biocompatible and bioresorbable polymer blend and composite filaments, for fused deposition modeling (FDM) printing. Poly(lactic acid) (PLA) and polycaprolactone (PCL) were used as supporting polymer matrix while hydroxyapatite (HA), a calcium phosphate with similar chemical composition to the mineral phase of human bone, was added to the composites to enhance the biological activity. PLA and PCL content was varied between 90–70 wt% and 10-30 wt%, respectively, while the HA content was 15 wt% in all composites. All materials were characterized in terms of mechanical properties, thermal stability, chemical composition and morphology. An accelerated degradation study of the materials was also executed in order to investigate the degradation behavior as well as the impact of the degradation on the above mentioned properties. The results showed that all processed materials exhibited higher mechanical properties compared to the human trabecular bone, even after degradation with a mass loss of around 30% for the polymer blends and 60% for the composites. It was also apparent that the mineral accelerated the polymer degradation significantly, which can be advantageous for injuries with faster healing time, requiring only support for a shorter time period.

Despite the recent development in PLA and PLGA based medical devices, there are still needs to further improve the mechanical performance of bioresorbable medical implants and their bioactivity. This is normally done by optimizing the filler compositions in selected groups ofbiodegradable polymer matrices. In this study, the effects of various filler levels on mechanical strength and thermal properties of PLA and PLGA composites were investigated. Composites containing different dosage of osteoconductive HAp with various particles size (0-5μm, 0-50 μm, nano size), β-TCP, bioactive glass and biodegradable Poly-L-lactide and Polylactide-glycolic acid was manufactured with melt blending, using a twin-screw extruder.The samples were investigated by Differential Scanning Calorimetry (DSC), thermo gravimetric analysis (TGA), Scanning Electron Microscopy (SEM), viscometer, three points bending machine, and Optical Microscopy (OM). The Extruder produced a porous profile. The result from TGA and SEM indicated that there was homogenous filler dispersion in the matrix after compounding.The result from DSC and Viscometer shows that there was some degradation duringcompounding. Mechanical properties of composites were modified by adding filler to matrix. The addition of Bioactive glass, as a filler, increases the degradation of the polymer matrix. The best filler that was applied is 0-5μm and nano HAp. Also in in-vitro degradation part of this thesis work, the effects of calcium phosphate materialsare investigated on degradation process.

In recent years, due to growing environmental awareness, considerable attention has been given to the development and production of natural fibre reinforced polymer (both thermoset and thermoplastic) composites. The main objective of this study was to reinforce epoxy and polylactic acid (PLA) with hemp fibre to produce improved composites by optimising the fibre treatment methods, composite processing methods, and fibre/matrix interfacial bonding. An investigation was conducted to obtain a suitable fibre alkali treatment method to: (i) remove non-cellulosic fibre components such as lignin (sensitive to ultra violet (UV) radiation) and hemicelluloses (sensitive to moisture) to improve long term composites stability (ii) roughen fibre surface to obtain mechanical interlocking with matrices (iii)expose cellulose hydroxyl groups to obtain hydrogen and covalent bonding with matrices (iv) separate the fibres from their fibre bundles to make the fibre surface available for bonding with matrices (v) retain tensile strength by keeping fibre damage to a minimum level and (vi) increase crystalline cellulose by better packing of cellulose chains to enhance the thermal stability of the fibres. An empirical model was developed for fibre tensile strength (TS) obtained with different treatment conditions (different sodium hydroxide (NaOH) and sodium sulphite (Na2SO3) concentrations, treatment temperatures, and digestion times) by a partial factorial design. Upon analysis of the alkali fibre treatments by single fibre tensile testing (SFTT), scanning electron microscopy (SEM), zeta potential measurements, differential thermal analysis/thermogravimetric analysis (DTA/TGA), wide angle X-ray diffraction (WAXRD), lignin analysis and Fourier transform infrared (FTIR) spectroscopy, a treatment consisting of 5 wt% NaOH and 2 wt% Na2SO3 concentrations, with a treatment temperature of 120oC and a digestion time of 60 minutes, was found to give the best combination of the required properties. This alkali treatment produced fibres with an average TS and Young's modulus (YM) of 463 MPa and 33 GPa respectively. The fibres obtained with the optimised alkali treatment were further treated with acetic anhydride and phenyltrimethoxy silane. However, acetylated and silane treated fibres were not found to give overall performance improvement. Cure kinetics of the neat epoxy (NE) and 40 wt% untreated fibre/epoxy (UTFE) composites were studied and it was found that the addition of fibres into epoxy resin increased the reaction rate and decreased the curing time. An increase in the nucleophilic activity of the amine groups in the presence of fibres is believed to have increased the reaction rate of the fibre/epoxy resin system and hence reduced the activation energies compared to NE. The highest interfacial shear strength (IFSS) value for alkali treated fibre/epoxy (ATFE) samples was 5.2 MPa which was larger than the highest value of 2.7 MPa for UTFE samples supporting that there was a stronger interface between alkali treated fibre and epoxy resin. The best fibre/epoxy bonding was found for an epoxy to curing agent ratio of 1:1 (E1C1) followed by epoxy to curing agent ratios of 1:1.2 (E1C1.2), 1: 0.8 (E1C0.8), and finally for 1:0.6 (E1C0.6). Long and short fibre reinforced epoxy composites were produced with various processing conditions using vacuum bag and compression moulding. A 65 wt% untreated long fibre/epoxy (UTLFE) composite produced by compression moulding at 70oC with a TS of 165 MPa, YM of 17 GPa, flexural strength of 180 MPa, flexural modulus of 10.1 GPa, impact energy (IE) of 14.5 kJ/m2, and fracture toughness (KIc) of 5 MPa.m1/2 was found to be the best in contrast to the trend of increased IFSS for ATFE samples. This is considered to be due to stress concentration as a result of increased fibre/fibre contact with the increased fibre content in the ATFE composites compared to the UTFE composites. Hygrothermal ageing of 65 wt% untreated and alkali treated long and short fibre/epoxy composites (produced by curing at 70oC) showed that long fibre/epoxy composites were more resistant than short fibre/epoxy composites and ATFE composites were more resistant than UTFE composites towards hygrothermal ageing environments as revealed from diffusion coefficients and tensile, flexural, impact, fracture toughness, SEM, TGA, and WAXRD test results. Accelerated ageing of 65 wt% UTLFE and alkali treated long fibre/epoxy (ATLFE) composites (produced by curing at 70oC) showed that ATLFE composites were more resistant than UTLFE composites towards hygrothermal ageing environments as revealed from tensile, flexural, impact, KIc, SEM, TGA, WAXRD, FTIR test results. IFSS obtained with untreated fibre/PLA (UFPLA) and alkali treated fibre/PLA (ATPLA) samples showed that ATPLA samples had greater IFSS than that of UFPLA samples. The increase in the formation of hydrogen bonding and mechanical interlocking of the alkali treated fibres with PLA could be responsible for the increased IFSS for ATPLA system compared to UFPLA system. Long and short fibre reinforced PLA composites were also produced with various processing conditions using compression moulding. A 32 wt% alkali treated long fibre PLA composite produced by film stacking with a TS of 83 MPa, YM of 11 GPa, flexural strength of 143 MPa, flexural modulus of 6.5 GPa, IE of 9 kJ/m2, and KIc of 3 MPa.m1/2 was found to be the best. This could be due to the better bonding of the alkali treated fibres with PLA. The mechanical properties of this composite have been found to be the best compared to the available literature. Hygrothermal and accelerated ageing of 32 wt% untreated and alkali treated long fibre/PLA composites ATPLA composites were more resistant than UFPLA composites towards hygrothermal and accelerated ageing environments as revealed from diffusion coefficients and tensile, flexural, impact, KIc, SEM, differential scanning calorimetry (DSC), WAXRD, and FTIR results. Increased potential hydrogen bond formation and mechanical interlocking of the alkali treated fibres with PLA could be responsible for the increased resistance of the ATPLA composites. Based on the present study, it can be said that the performance of natural fibre composites largely depend on fibre properties (e.g. length and orientation), matrix properties (e.g. cure kinetics and crystallinity), fibre treatment and processing methods, and composite processing methods.

Le traitement du cancer est l’un des plus grands défis en chimie médicinale moderne. La majorité des traitements utilisés repose sur la chimiothérapie, impliquant l’emploi de molécules bioactives cytotoxiques. Bien qu’efficaces, ces molécules présentent, pour la plupart, des désavantages notoires tels que le manque de spécificité cellulaire et une solubilité limitée en phase aqueuse. Une façon de remédier aux problèmes exposés est de solubiliser ces molécules au sein de matrices polymères. Il existe différents types de matrices qui sont : les liposomes, les micelles, les nanosphères, les nanocapsules, les dendrimères (et les polymères en étoile), et les polymères conjugués et linéaires. Dans cette thèse, nous faisons l’étude de deux matrices polymères potentielles composées de matériaux biocompatibles : le polylactide et la poly(2-isopropyl-2-oxazoline). La première partie de la thèse, est consacrée à l’étude des polyester-co-éthers portant des groupements pendants fonctionnalisables. Nous avons développé ces copolymères par polymérisation aléatoire en masse de lactones (le lactide ou la caprolactone) et différents taux d’éthers de propargyle et de glycidyle (GPE), à 120°C, en utilisant l’octanoate d’étain comme catalyseur. L’efficacité de la copolymérisation a été mise en évidence par des analyses FTIR, RMN 1H et COSY. Toutefois, L’analyse GPC a montré une diminution de la masse molaire des polymères et un élargissement de la dispersité en rapport avec l’augmentation du taux de glycidyle initial. De plus, les analyses RMN 1H ont montré que le taux de propargyl (provenant de l’éther de glycidyle) au sein du copolymère ne dépassait pas 50%. La faisabilité des modifications post-polymérisation a été évaluée en couplant le (9-azidomethyl) anthracène au chaîne de poly(ester-co-éther)s via la chimie clic CuAAC. Cette méthode s’est révélée inoffensive pour la chaîne de polyesters. Des études de cytotoxicité ont prouvé l’innocuité des poly(ester-co-éther)s. Des nanoparticules sphériques ont été préparées à partir de ces polymères et peuvent être utilisées comme nanosphères pour le transport de molécules bioactives hydrophobes. La copolymérisation des lactones avec des éthers de glycidyles s’avère être une stratégie intéressante de fonctionnalisation des chaînes des polyesters permettant la synthèse d’une large gamme de copolymères pour des applications biomédicales. Afin d’améliorer la synthèse des poly(ester-co-ether)s, nous avons proposé une approche mécanistique tenant compte des réactions de transfert de chaînes. Dans la deuxième partie de la thèse, nous avons étudié un polymère en étoile composé d’un polymère thermosensible : la poly(2-isopropyl-2-oxazoline) PIPOZ. Nous avons premièrement exploré deux approches synthétiques afin d’obtenir une série d’étoiles de PIPOZ (S-PIPOZ) de structure bien définié à savoir l’approche « coupling-onto » et l’approche « core-first ». Une première série de S-PIPOZ a été réalisée directement à partir d’un coeur pentaérythrityl tétratosylés par polymérisation cationique par ouverture de cycle (CROP) de 2-isopropyl-2-oxazoline pour l’approche « core-first ». Pour l’approche « coupling-onto », une deuxième série de S-PIPOZ a été réalisée par couplage via la CuAAC entre des PIPOZ-N3 linéaire (L-PIPOZ N3) et un cœur à 4 bras portant des alcynes terminaux. Tous les S-PIPOZs obtenus ont été analysés par RMN 1H, IR, MALLS-LS, des analyses UV et par microcalorimétrie différentielle à balayage (HS-DSC). Les polymères obtenus par l’approche « core-first » ont montré une microstructure mal-définie comparé à ceux obtenus par l’approche « coupling-onto ». Suite à ces résultats, nous avons défini l’approche « coupling-onto » comme voie d’obtention des S-PIPOZ. Une explication sur la structure mal-défini des polymères obtenus par l’approche « core-first » sera développée dans cette section. Nous exposerons aussi une méthode de purification permettant l’élimination rapide et efficace des L-PIPOZ N3 qui contaminent les échantillons de S-PIPOZ faits par l’approche « coupling-onto ». Cette méthode peut être applicable à d’autres polymères thermosensibles dans une certaine gamme de température. Dans la troisième partie, nous avons étudié l’effet de l’architecture et de la composition des bras-polymères sur la température de transition de phase et les propriétés des S-PIPOZs. Afin d’étoffer notre étude nous avons synthétisé un polymère en étoile à bloc composé de PIPOZ et de poly(éthylène glycol) PEG. Cette étude a été réalisée en examinant des solutions chauffées de polymères (S-PIPOZ, S-PIPOZ-b-PEG et tous les précurseurs linéaires) par des analyses de spectrométrie d’absorption UV, HS-DSC, diffusion de la lumière LS. Nous avons évalué la présence ou l’absence de cristaux au sein d’échantillons de S-PIPOZs provenant de solutions chauffées. Cette évaluation a été réalisée par diffusion des rayons-X aux grands angles (WAXS) et par microscopie électronique à transmission (TEM) et à balayage (SEM). La présence de cristaux est néfaste pour la conception de nanomatériaux destinés à des applications biomédicales. Nous exposons aussi dans cette section une méthode basée sur l’amination réductrice permettant de fonctionnaliser les S-PIPOZ avec différents types de macromolécules. Cette thèse expose les avantages et les inconvénients (synthèses, fonctionnalisation, structures…) des PLA-co-GPE et des S-PIPOZs et constitue dans son ensemble à une première ébauche vers une conception améliorée de futurs nanomatériaux. / Treatment of cancer is one of the biggest challenges in modern medicinal chemistry. The vast majority of treatments are based on chemotherapy, involving the use of cytotoxic bioactive molecules. Although effective, most of these bioactive molecules have notorious drawbacks, such as the lack of cellular specificity and limited solubility in aqueous media. A way to address these problems is to dissolve these bioactive compounds into polymer matrices. There are different types of matrices, including liposomes, micelles, nanospheres, nanocapsules, dendrimers (and star-polymers), and conjugate and linear polymers. In this thesis, we explored two different prospective polymers that can be used as matrices. Both are composed of biocompatible materials: polylactide and poly(2-isopropyl-2-oxazoline). The first part of the thesis is dedicated to the investigation of polyester-co-ether with functionalizable pendant groups. First, we developed the polyester-co-ether by copolymerization of lactones (lactide or caprolactone) with different ratios of glycidyl propargyl ether (GPE) in the bulk at 120°C in the presence of Sn(Oct)2. The efficiency of the copolymerization was evidenced by FTIR, 1H and COSY NMR analyses. However, GPC analyses displayed a decrease of molecular weights and a broadening of the molecular weight dispersity with increasing of the epoxide molar ratio in the feed. 1H NMR analyses showed that the propargyl content from the epoxide does not exceed 50%. The feasibility of post-polymerization functionalization was evaluated by coupling anthracene to the poly(ester-co-ether)s through copper-catalyzed alkyne-azide cycloaddition (CuAAC). The polyester chain was found to support this reaction. Toxicity studies showed that the poly(ester-co-ether) was non-toxic. Spherical nanoparticles were prepared from these polymers. They can be suitable nanospheres for drug delivery. The copolymerization of lactone with glycidyl ether is an interesting approach to functionalize the PLA (or poly(ester)) main chain. It is also a powerful and straightforward strategy to synthesize a large array of functionalized polymers for biomedical applications. In order to improve the synthesis of the polyester-co-ether, we investigated the copolymerization mechanism of the chain transfer reactions leading to the chain reductions and we suggested a mechanistic explanation. In the second part of this thesis, we focused on developing star-polymers from the thermosensitive (2-isopropyl-2-oxazoline) polymer. In order to prepare a well-defined set of star-poly(2-isopropyl-2oxazoline) S-PIPOZs, we explored two different synthetic approaches: the “coupling-onto” and the “core-first” approach. Two sets of S-PIPOZs were prepared by these approaches. For the “core-first” approach, a set of S-PIPOZ was prepared by direct cationic ring opening polymerization (CROP) from a tetra tosylate-functionnalized pentaerythrityl core. For the “coupling-onto approach”, the S-PIPOZs were prepared by ligation between L-PIPOZ-N3 and a 4-arm core with an alkyne group via CuAAC. The prepared polymers were analysed by 1H NMR, IR, Multi Angles Laser Light Scattering - Gel Permeation Chromatography (MALLS-GPC), UV absorption spectroscopy and High Sensitive Differential Scanning Microcalorimetry (HS-DSC). Polymers obtained by the “core-first” approach shows ill-defined microstructure compared to those obtained by the “coupling-onto” approach. In light of these encouraging results, the “coupling-onto” method was pursued for preparing S-PIPOZ. An explanation on the ill-defined structure will be provided within this thesis. Moreover, we developed a purification method for the fast and efficient removal of free PIPOZs, which otherwise contaminate the star-PIPOZ samples that are prepared by the coupling-onto approach. This method is applicable to other thermosensitive polymers within a certain range of temperature. In the third part, we focused on the effect of the architecture and composition of the S-PIPOZs on the phase transition temperature of the polymer. For this, we synthesized a hetero-star block copolymer composed of PIPOZ and poly(ethylene glycol) PEG. This study was carried out by examining the aqueous polymer solution (the linear precursors, S-PIPOZs, S-PIPOZ-b-PEG) upon heating via UV spectroscopy, HS-DSC and light scattering. We also assessed the temperature-induced crystallinity of the Star-PIPOZs by Transmission (TEM) and Scanning (SEM) Electron Microscopy, WAXS. This is important for biomedical nanodevices. We also provided a straightforward method, based on aminative reduction, to functionalize the S-PIPOZ with different macromolecules. This thesis discusses the advantages and the drawbacks related to the synthesis, functionalization, structures of PLA-co-GPE and the star-PIPOZs. Overall, this represents a pioneering study for improving the design of prospective nanodevices.