Over the past two decades one class of oligomers, polyhedral oligomeric silsesquioxanes (POSS), has attracted considerable attention because of their unique hybrid organic/inorganic molecular structures and nanoscopic sizes. While surface and interfacial properties may play a key role in many potential POSS applications, relatively little is actually known about the surface properties of POSS. This dissertation provides studies of the interfacial aspects of both POSS molecules and POSS/polymer blends at the air/water interface (A/W) through surface pressure-area per molecule (π-<i>A</i>) isotherm, Brewster angle microscopy (BAM), and interfacial stress rheometry (ISR) studies. Results for POSS Langmuir thin films at A/W show that trisilanol-POSS derivatives are a new class of amphiphiles, that exhibit multiple phase transitions in going from traditional 2D Langmuir monolayers (1 POSS molecule thick) to various 3D multilayer films upon compression. With small length/diameter ratios and bulky shapes, the monolayer phase behavior and packing states of different POSS are simpler than the traditional rod-like lipids. Meanwhile trisilanol-POSS derivatives have very different collapse behavior and multilayer organization showing strong substituent effects even though they have similar molecular sizes. While trisilanolisobutyl-POSS (TiBuP) monolayers undergo collapse around π ≈ 18 mNm⁻¹ and form various ordered or disordered solid-like 3D aggregates at different compression rates, trisilanolcyclohexyl-POSS (TCyP) monolayers collapse into trilayers via instantaneous nucleation with hemispherical edge growth around π ≈ 3.7 mNm⁻¹. ISR results reveal three different non-Newtonian flow regimes that correlate with phase transitions in the Pi-A isotherms. Further symmetric compression after trilayer formation induces TCyP thin films to self-assemble into highly ordered crystalline-like hydrophobic multilayers (≈8 POSS molecule thick) with unique rod-like morphologies, which are dramatically different from –collapsed– morphologies seen in other systems. By treating POSS derivatives as ideal nanofiller for studying confinement effects on filled polymer systems, amphiphilic poly(dimethylsiloxane) (PDMS) derivatives with different polar functional groups are studied as blends with TiBuP and octaisobutyl-POSS at A/W to resolve one of the key challenges for current nanocomposite applications: How to control nanofiller dispersion in polymer matrices? The results in this dissertation reveal that introducing polar groups into polymeric matrix polymers is a good way to control dispersion. / Ph. D.

Filament-based material extrusion additive manufacturing (MEAM) is an established technique in additive manufacturing (AM). However, semicrystalline polymers, such as polypropylene (PP), have limited commercial use in MEAM processes in the past due to their rapid crystallization kinetics and the subsequent effect on the integrity of the generated structures. The rapid crystallization of PP can be controlled by formulating blends of PP with hydrocarbon resins to enable longer re-entanglement times for interlayer adhesion. While the topic of formulating PP blends/composites with other materials to improve the printability has been investigated, variation in properties of commercial PP grades, of similar molecular weight (MW) and molecular weight distribution (MWD), on printability is still to be investigated. Those commercial PP grades can have wide variation in properties such as Melt Flow Index (MFI), additive content, and polymer architecture which can impact material properties relevant to printability. To investigate the effect of properties of commercial PP on their printability and mechanical performance, different commercial PP grades, with different properties, are blended with a fixed loading of hydrogenated resins, and the consequent effects on the mechanical properties of MEAM generated PP structures are studied via mechanical analysis. Tensile strength and the extent of interlayer adhesion in the 3D printed blends are characterized through rheological measurements. These measurements emphasize the importance of the relative location of the storage/loss modulus crossover point via small oscillatory frequency sweeps. We specifically show that a relatively higher crossover frequency will correlate with improved interlayer adhesion and reduced warpage in printed structures. However, this improvement is accompanied by a tradeoff, resulting in inferior tensile strength and an increased degree of print orientation anisotropy. / Master of Science / Additive Manufacturing (AM), commonly known as 3D printing, is a transformative technology with high potential to revolutionize the manufacturing landscape. Polymers are widely used in AM for various applications. As a result, extensive research is conducted to enhance the printability and properties of printed polymer structures. Polypropylene (PP) exhibits desirable mechanical, optical, and chemical properties that make its use in AM attractive. Despite this potential, optimizing the use of PP in 3D printing remains challenging. Consequently, extensive research is underway to improve the printability of PP. However, the effects of including additives to enhance the properties of commercial PP grades are often overlooked. We demonstrate that the choice of commercial PP grade is crucial to the mechanical and structural properties of structures generated via AM. This was established by developing a systematic experimental procedure to assess the printability of various PP grades and to measure their key mechanical and structural properties.

Ternary blends comprising Polysulphones [Polyethersulphone (PES) and Polysulphone (PSO)], the Polyhydroxyether of bisphenol-A (Phenoxy), and Polyesters [Poly( ethylene terephthlate) (PET) and Poly(butylene terephthlate) (PBT)] have been studied particularly with the aim in mind of elucidating the factors determining their miscibility and morphology. Binary and ternary combinations, including equivalent systems based on a butylene terephthlate-tetramethylene oxide block copolymer (PBT-TMO), were prepared from solution and by mixing in the melt state using both an internal mixer and a twin screw extruder. Scanning electron microscopy was employed to examme the morphology of these blends. A co-continuous, (interpenetrating), dual-phase morphology was displayed by both the PSO/PBT and PSO/PBT-TMO (70/30) combinations. The compatibility was further increased by the addition of Phenoxy, which was evidenced by the formation of a very fine dispersion of the two phases for both PSO/Phenoxy/PBT and PSO/Phenoxy/PBT-TMO blends, in the weight ratio of (60/15/25). A lower level of compatibility was displayed by the equivalent blends based on PES and PET, as a matrix/dispersed particle type of morpholgy was usually observed. Differential thermal analysis and dynamic mechanical analysis measurements were also employed to ascertain the level of miscibility in these systems. A single composition dependent glass transition temperature was displayed by the binary PBT/Phenoxy and PBT-TMO/Phenoxy melt blends, and the binary PES/Phenoxy and _PSO/Phenoxy solution blends. The remaining blends displayed two separate glass transition temperatures that were often broader and closer together than those of the homopolymers. This effect was more significant for blends containing the Phenoxy compatibiliser, confirming that these systems are semi-miscible. Solvent resistance measurements were made on 500μm thick extruded sheets by measuring the time to failure at stress levels corresponding to 30% and 50% of the tensile strength. The blends displaying a matrix/dispersed particle type of morphology revealed poor solvent resistance and mechanical properties. The blends displaying a cocontinuous interpenetrating dual-phase morphology on the other hand displayed a much higher solvent resistance and enhanced mechanical properties.

Les mélanges de polymères ouvrent une importante voie à l’obtention de nouveaux matériaux dont les propriétés peuvent être très différentes de celles de chacun des constituants des mélanges. La plupart des polymères sont immiscibles. Ainsi leurs mélanges constituent des phases distinctes et les propriétés de ces mélanges sont souvent médiocres. Afin de relever ce défi, copolymères à bloc ou greffés synthétisés séparément ou générés in-situ lors du procédé de mélanges sont souvent utilisés en tant que agents compatibilisants. Beaucoup d’études ont porté sur l’efficacité de compatibilisation de copolymères à bloc et peu d’études sur celle de copolymères greffés, en partie en raison des difficultés dans le contrôle de leurs structures moléculaires. Cette thèse porte sur l’étude de l’efficacité d’émulsification de copolymères greffés. Elle est composée de trois parties : (1) développement d’un nouveau procédé d’extrusion réactive pour la synthèse de copolymères greffés avec polystyrène (PS) comme squelette et polyamide 6 (PA6) comme greffons ; (2) efficacité d’émulsification du copolymère greffé, PS-g-PA6 pour les mélanges à base de PS et PA6 ; et (3) développement d’un nouveau concept dit d’agent émulsifiant – traceur / Polymer blending offers an important route to new materials with combinations of properties not available in constituent polymers. Most polymer pairs are immiscible, leading to phase separation at equilibrium and yield a material with poor properties. To address this challenge, block or graft copolymers pre-made or generated in-situ by reactive blending are often used as compatibilizers. Most studies are focused on the compatibilizing efficiency of block copolymers and few studies address that of graft copolymers, partly because of difficulties of controlling their molecular structures.This thesis is devoted to the study of the emulsification efficiency of graft copolymers. It is composed of three parts: (1) development of a novel reactive extrusion process for synthesizing graft copolymers with polystyrene (PS) as backbone and polyamide 6 (PA6) as grafts; (2) emulsification efficiency of PS-g-PA6 graft copolymers for PS/PA6 blends; and (3) concept of emulsifier- tracer

Le but de la thèse est de comprendre les mécanismes de localisation de particules (on parle de charges) dans des mélanges de polymères immiscibles. Ces travaux montrent que la localisation des charges de noir de carbone dans un mélange polypropylène (PP)/ poly-ε-caprolactone (PCL) est dominée par le rapport de viscosités et non par des paramètres thermodynamiques (liés au mouillage de la particule). La localisation des charges est expliquée par la compétition des forces de drainage visqueux s’exerçant sur les particules à l’interface. Le mécanisme de transfert des charges est mis en évidence par observation de la relaxation de gouttes de PCL chargées immergées dans une matrice PP. Le transfert se produit par un nouveau mécanisme, appelé « zip flow », qui consiste à l’érosion des gouttes au niveau des pointes. La maîtrise des différents paramètres étudiés permet de localiser les particules sélectivement à l’interface et d’obtenir des propriétés de conductivité à faible taux de charges. / The aim of this work is to understand mechanisms responsible for particles localisation in immiscible polymer blends. This study shows that carbon-black fillers localisation in polypropylene (PP)/ poly-ε-caprolactone (PCL) blends is strongly influenced by the viscosity ratio (rather than thermodynamic parameters through the wetting coefficient). The localisation of the fillers is explained by a competition of hydrodynamic forces applied on particles localised at the interface. The transfer of fillers is investigated at the droplet scale by observation of the relaxation of CB-filled PCL droplets suspended in PP matrix. CB particles are transferred from the PCL droplet to the PP matrix by a new mechanism, called “zip flow”, which involves the erosion of the droplet edges, leading to the extraction of particles localised there. The control of these parameters allows to localize fillers selectively at the interface and to reduce significantly the electrical percolation threshold.

L'objectif de ce travail de thèse est de fournir une étude systématique et détaillée des propriétés de mélanges de PLA et de PHA préparés à l'état fondu. En particulier, le comportement rhéologique, la miscibilité, la morphologie, les propriétés mécaniques et l'influence du vieillissement physique sur les propriétés en traction des mélanges PLA/PHBV réalisés en mélangeur interne et par extrusion bi-vis sur toute la gamme de composition ont été étudiés.La sensibilité du PHBV à la dégradation thermique a été mise en évidence, ainsi que l'importance des interfaces entre le PLA et le PHBV sur le comportement rhéologique aux basses fréquences. Les analyses de calorimétrie différentielle à balayage ont montré l'immiscibilité des deux polymères. Deux types de morphologies distinctes (nodulaire et co-continue) selon la composition de mélange ont été observées par microscopie électronique à balayage et microscopie optique en réflexion. La résistance au choc des mélanges PLA/PHBV avec et sans modifiant choc a été étudiée et les propriétés en traction de différents mélanges de PLA avec du PHBV, du Lotader GMA ou du PBAT ont été caractérisées. L'ajout d'une faible quantité de phase dispersée dans la matrice de PLA, initialement fragile, permet d'augmenter considérablement son allongement à la rupture. Cependant, les propriétés ductiles obtenues diminuent avec le temps écoulé entre la mise en forme des échantillons et leur test mécanique. Une étude de l'influence du vieillissement physique sur les propriétés des mélanges à base de PLA a donc été réalisée et un modèle qualitatif a été proposé. / The objective of this PhD work is to provide a systematic and detailed study of the properties of PLA and PHA blends prepared by melt mixing. In particular, the rheological behaviour, the miscibility, the morphology, the mechanical properties and the influence of physical aging on the tensile properties of PLA/PHBV blends prepared in an internal mixer and by twin screw extrusion over the entire composition range were studied.The sensibility of PHBV to thermal degradation was highlighted, as well as the importance of the interfaces between PLA and PHBV on the rheological behaviour at low frequencies. The differential scanning calorimetry showed that the two polymers are immiscible. Two different types of morphologies (nodular and co-continuous) depending on blend composition have been observed by scanning electron microscopy and optical microscopy in reflection. The impact resistance of the PLA/PHBV blends with or without impact modifier was studied and the tensile properties of different blends containing PLA blended with PHBV, Lotader GMA, or PBAT were characterised. The addition of a small amount of dispersed phase in the initially brittle PLA matrix increases considerably its elongation at break. However, the obtained ductile properties decrease as the time between preparation of samples and their mechanical testing increases. A study of the influence of physical aging on the properties of PLA based blends was conducted and a qualitative model was proposed.

L’acide polylactique (PLA) est l’un des polymères biosourcés qui suscite le plus d’intérêt, mais ses propriétés thermomécaniques nécessitent d’être améliorées. Pour ce faire, les méthodes les plus utilisées et étudiées sont de le mélanger avec d’autres polymères ou bien d’y ajouter des charges minérales nanométriques (nanoparticules), afin de constituer un nanocomposite à matrice PLA. C’est dans la combinaison de ces deux approches que s’inscrivent ces travaux de thèse, consacrés à l’élaboration et à la caractérisation des propriétés de nanocomposites à base d’un alliage de PLA et de polyamide 11 (PA11) 80/20 m/m. L’objectif de cette thèse est l’obtention d’un matériau biosourcé aux propriétés thermiques, mécaniques et de réaction au feu améliorées par le contrôle de sa morphologie et l’ajout de nanoparticules et de retardateurs de flamme (RF). Pour y parvenir, deux techniques de compatibilisation, destinées à améliorer l’adhésion interfaciale entre le PLA et le PA11, ont été évaluées. La première consistait à incorporer des nanoparticules de silice. Il a été noté d’importantes modifications de la morphologie et des propriétés rhéologiques du mélange d’étude, selon leur localisation dans le mélange étudié fonction de la nature chimique de la surface de la silice. La deuxième consistait à introduire un copolymère époxyde multifonctionnel réactif, dénommé Joncryl. La réactivité de ce copolymère avec le PLA et le PA11 a permis de compatibiliser le mélange d’étude, conduisant à une morphologie plus fine et à l’obtention de propriétés mécaniques supérieures à celles du mélange d’étude, en particulier avec l’ajout de 3%m de Joncryl. Des échantillons basés sur les mélanges compatibilisés par cette méthode ont été préparés par le procédé de fabrication additive FDM. Une étude de l’impact de ce procédé sur la morphologie et les propriétés mécaniques obtenues a été entreprise. Enfin, une meilleure réaction au feu pour le mélange compatibilisé avec 3%m de Joncryl a pu être obtenue par l’ajout combiné de nanoparticules de phyllosilicates et de RF. / Polylactic acid (PLA) is one of the biobased polymers that generates the most interest, but its thermomechanical properties need to be improved. To do that, the most used and studied methods consist of blending PLA with other polymers or adding nanoscaled mineral fillers (nanoparticles) to get a PLA based nanocomposite. This PhD work is dedicated to the elaboration and properties characterization of nanocomposites based on a filled PLA and polyamide 11 80/20 wt/wt blend. The aim is to obtain a biobased material with improved thermal, mechanical and fire reaction properties by controlling its morphology through the addition of nanoparticles and flame retardants additives.To achieve that, two compatibilization techniques, aiming to improve PLA-PA11 interfacial adhesion, were evaluated. The first one consisted of adding silica nanoparticles. Important changes of the blend morphology and rheological properties were noticed, depending on the localization of the two different silica nanoparticles used into the polymer blend phases. The second one consisted of introducing a reactive multifunctional epoxy copolymer, named Joncryl. The reactivity of this copolymer with PLA and PA11 allowed to compatibilize the blend, leading to a fine morphology and higher mechanical properties compared to those of the pristine blend. Samples of compatibilized blends obtained through this method were processed using FDM additive manufacturing process. A study of the influence of this process on the morphology and mechanical properties obtained for these samples was performed. Finally, a better fire reaction of compatibilized polymer blend with 3%wt Joncryl was obtained by the combined addition of phyllosilicates nanoparticles and flame retardants.

L’objectif de cette thèse est d’investiguer la miscibilité des mélanges de polymères dans une perspective de recycler les polymères issus des DEEE par rotomoulage. En effet, la miscibilité est un facteur clé qui conditionne les propriétés finales du mélange. Basé sur les résultats de caractérisation des flux DEEE d’Éco-systèmes, le choix des matériaux d’étude (PVDF/PMMA) et (ABS/PC) a été motivé par l’intérêt à la fois industriel et scientifique de ces deux couples. La première partie du travail présente une panoplie de méthodes expérimentales mises en place, allant des procédés de mise en œuvre à la caractérisation des matériaux dans le but d’explorer in fine la miscibilité de ces mélanges. En particulier, l’étude de la coalescence des grains a permis de mettre en évidence la miscibilité du couple PVDF/PMMA et la miscibilité partielle de l’ABS/PC (phénomène d’enrobage). À l’issu de cette étude, le couple PVDF/PMMA a été retenu en tant que couple « modèle » pour mettre en place un modèle prédictif généralisé de la coalescence entre grains de polymères différents. Ce modèle a été couplé à une étude probabiliste paramétrique des incertitudes permettant d’évaluer l’effet des incertitudes des mesures relatives à la viscosité, la tension de surface, le temps de relaxation et la taille des grains sur la cinétique de coalescence. Le travail se termine par une ébauche de la simulation du phénomène de coalescence et de l’enrobage dans le cas des polymères miscibles et partiellement miscibles. / The aim of this thesis is to study the miscibility of polymer blends with a view to recycling WEEE polymers by rotomoulding. Indeed, miscibility is a key factor which determines the final properties of polymer blends. The work was divided into two parts. Based on the characterization results of Éco-systèmes WEEE, the choice of materials (PVDF / PMMA) and (ABS / PC) was motivated by the industrial and scientific interest of these two couples. The first part of the work presents an array of experimental methods, ranging from processing to material characterization, with the aim of exploring the miscibility of these mixtures. In particular, the study of the coalescence of the grains made it possible to demonstrate the miscibility of the PVDF / PMMA couple and the partial miscibility of the ABS / PC (coating phenomenon). At the end of this study, the PVDF / PMMA couple was retained as a "model" pair to perform a generalized predictive model of the coalescence between different polymer grains. This model was coupled with a probabilistic parametric analysis to evaluate the effect of the uncertainties of the viscosity, surface tension, relaxation time and grain size measurements on coalescence kinetics. The work ends with a draft of the simulation of the coalescence phenomenon and the coating in the case of miscible and partially miscible polymers respectively

Neste trabalho, foi estudado o comportamento reológico nos regimes de viscoelasticidade linear (VEL) e não linear (VENL) da mistura polimérica de polimetacrilato de metila/poliestireno (PMMA/PS), compatibilizada ou não com os copolímeros: estatístico P(S-co-MMA) (VEL e VENL) e bloco P(S-b-MMA) (VEL). No estudo do comportamento de VEL, ensaios de cisalhamento oscilatório de pequenas amplitudes (COPA) foram realizados utilizando-se um reômetro de tensão controlada. O comportamento de VEL das misturas poliméricas foi comparado com os modelos teóricos de Bousmina[1] e generalizado de Palierne[2]. Os tempos de relaxação das misturas poliméricas foram obtidos analisando o comportamento reológico no regime de VEL utilizando o software desenvolvido por Honerkamp e Weese[3]. Os tempos obtidos foram comparados com o modelo de Jacobs et al.[4]. O estudo do comportamento de VENL foi conduzido através de ensaios de relaxação de tensão utilizando-se um reômetro de deformação controlada. Os resultados do comportamento reológico no regime de VEL indicaram a presença de quatro tempos de relaxação, para as blendas compatibilizadas com P(S-co- MMA) (composições menores de 10% de fase dispersa e concentrações maiores de 4% de copolímero): dois picos relacionados às fases puras; F, relacionado com a relaxação das gotas da fase dispersa e o relacionado com a relaxação do compatibilizante na interface entre as fases matriz e dispersa. Os valores experimentais de F e foram utilizados para os cálculos de tensão interfacial () e do módulo complexo de interface () das blendas poliméricas compatibilizadas. Os resultados indicaram uma diminuição de com o aumento da concentração de copolímero. Os resultados do comportamento reológico no regime de VEL, para as blendas compatibilizadas com P(S-b-MMA), também apresentaram a presença de quatro tempos de relaxação. Observou-se que o aumento da adição de P(S-b-MMA) proporcionou uma redução no .. Os resultados de VENL de relaxação de tensão mostraram a presença de três fenômenos de relaxação, relacionados com: 1) as fases puras, 2) a relaxação das gotas da fase dispersa e um terceiro mais rápido. A adição de P(S-co-MMA) resultou numa diminuição do processo de relaxação das gotas da fase dispersa. / In this work, the dynamic behavior of polymethylmetacrylate/polystyrene (PMMA/PS) blends to which P(S-co-MMA) was added was studied. Several blend composition and copolymer concentrations were studied. The rheological behavior of blends was compared to Bousminas[1] and Paliernes generalized[2] models. The relaxation spectra of the blends were also inferred, and the results were analyzed in light of the analysis of Jacobs et al.[4]. The relaxation spectra of the blends with smaller dispersed phase (below 10 wt%) and larger copolymer concentrations (above 0.4 wt%) showed the presence of four relaxation times, two corresponding to the blend phases, F, corresponding to the relaxation of the shape of the dispersed phase of the blend, and , that can be attributed to the relaxation of Marangoni stresses tangential to the interface between the dispersed phase and matrix. The experimental values of F and were used to infer the interfacial tension () and the interfacial complex shear modulus () for the different blends, decreased with increasing copolymer concentration. decreased with increasing blend dispersed phase concentration and decreasing copolymer concentration. The predictions of Paliernes generalized model were found to corroborate the experimental data once the values of and found analyzing the relaxation spectra were used in the calculations. Bousminas model was found to corroborate the data only for larger dispersed phase concentration. The stress relaxation behavior of PMMA/PS blends with or without random copolymer addition, submitted to step shear strain experiments in the linear and nonlinear regime was studied. The effect of blend composition, viscosity ratio and random copolymer was evaluated. All blends presented three relaxation stages, a first relaxation which was attributed to the relaxation of the pure phases, a second one which was characterized by the presence of plateau and a third fast one.

O descarte inadequado de embalagens poliméricas tem gerado uma grande preocupação mundial. O alto consumo, atrelado ao curto tempo de uso dessas embalagens tem ocasionado um grande passivo ambiental. Diferentemente dos usuais polímeros empregados para este propósito, o poli(ácido lático) ou PLA é de fonte renovável e pode ser degradado no meio ambiente por ação de microrganismos como bactérias e fungos. Possui grande potencial para produzir sustentavelmente novos tipos de embalagens que sejam ambientalmente amigáveis. No entanto, para isso é preciso modificar algumas propriedades mecânicas para satisfazer sua aplicação, como a ductilidade e tenacidade. Uma boa alternativa para superar essas limitações é misturá-lo mecanicamente a um segundo polímero, produzindo blendas com propriedades melhoradas. Neste trabalho foram preparadas blendas poliméricas entre o PLA e o copolímero aleatório poli[(etileno)-co-(acetato de vinila)] (EVA), com teores de acetado de vinila (VA) de 65% (EVA65) e 90% (EVA90). As blendas foram preparadas por extrusão em dupla rosca co-rotacional interpenetrante. A morfologia e miscibilidade das blendas PLA/EVA foram estudadas por microscopia eletrônica de varredura (MEV), calorimetria exploratória diferencial (DSC) e análise termodinâmico-mecânica (DMTA). As propriedades mecânicas foram avaliadas por ensaios de tração, flexão em três pontos e resistência ao impacto Izod com entalhe. A influência do teor de VA na biodegradabilidade do PLA foi avaliada por perda de massa e por propriedades mecânicas em tração dos corpos de prova que foram submetidos ao teste de biodegradação em solo e ficaram enterrados por 0, 30, 90, 120 e 150 dias. As curvas DSC e os resultados de DMA mostram que as blendas PLA/EVA90 apresentam uma única temperatura de transição vítrea (Tg), sendo, portanto, miscíveis. Entretanto, as blendas PLA/EVA65 apresentam duas Tg e nítida separação de fases comprovando que são imiscíveis em todas as frações testadas. Mudanças como deslocamento da temperatura de cristalização do PLA são influenciados pelo aumento do teor de EVA nas blendas. Todas as blendas apresentam melhora nos resultados de flexibilidade e deformação na ruptura, destaque para amostra contendo 20% de EVA65 onde a deformação na ruptura foi 350% maior que o PLA puro. A resistência ao impacto da blenda contendo 30% de EVA65 representou um aumento na tenacidade aproximadamente 2400% em relação ao valor obtido pelo PLA puro. A taxa de biodegradação do PLA foi reduzida com o aumento do teor de EVA nas blendas. Blendas com EVA90 obtiveram maiores perdas de massa que as equivalentes contendo EVA65, revelando também a influência da miscibilidade na taxa de biodegradação do PLA. No entanto, ao final de 180 dias todos os corpos de provas sofreram variação negativa da massa, ou seja, foram biodegradados no solo. / The inadequate disposal of packaging materials has led to a major worldwide concern. The high consumption, together with the short usage time of packaging materials, has created a serious environmental issue. Unlike conventional polymers, poly(lactic acid) or PLA comes from a renewable source and can be degraded by microorganisms (e.g., bacteria and fungi) in the environment. PLA has a great potential for the sustainable development of environmentally friendly materials intended for packaging applications. To do so, however, some of its mechanical properties (e.g., ductility and toughness) must be modified to meet the technical requirement for such applications. A feasible alternative of overcoming these limitations is mechanically blending PLA with a second polymer, producing blends featuring improved properties. In this study, we prepared polymer blends by mixing PLA and the random copolymer poly[(ethylene)-co-(vinyl acetate)] (EVA) comprising vinyl acetate (VA) contents of 65% (EVA65) and 90% (EVA90). The blends were prepared through interpenetrating co-rotating twin screw extrusion. PLA/EVA blend morphology and miscibility were investigated through scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and dynamic thermomechanical analysis (DMTA). Mechanical properties were determined through tensile, three-point bending, and notched Izod impact strength tests. The influence of VA content on PLA biodegradability was assessed by weight loss measurements as well as tensile tests in specimens submitted to biodegradation in soil, wherein they remained covered for 0, 30, 90, 120, and 150 days. DSC curves and DMTA data showed that the PLA/EVA90 blends presented a single glass transition temperature (Tg), indicating miscibility. On the other hand, the PLA/EVA65 blends presented two Tg as well as marked phase separation, corroborating the immiscibility of all tested fractions. Shifts on the crystallization temperature of PLA are influenced by increased EVA contents in the blends. All blends showed improved flexibility and deformation at break, particularly that comprising 20% EVA65, which presented an elongation at break 350% higher than pristine PLA. The impact strength of the blend comprising 30% EVA65 evidenced a ca. 2400% increase in toughness in comparison with pure PLA. PLA biodegradation rate was reduced by increased EVA contents. EVA90-containing blends displayed greater weight losses than their EVA65-containing counterparts, also revealing the influence of miscibility on PLA biodegradation rate. Nevertheless, after 180 days, all specimens presented weight loss, that is, were biodegraded in soil.