Tesis por compendio / [ES] Se han desarrollado mediante termoprocesado películas multicapa biodegradables activas para el envasado de alimentos, combinando películas de almidón mejoradas y de una mezcla de poliésteres (PLA-PHBV), con diferentes ácidos fenólicos (ferúlico, p-cumárico y protocatecuico). En las películas almidón de yuca o de maíz se incorporaron gomas de origen microbiano (xantana y gelano) (10%) para mejorar sus propiedades funcionales. Las gomas mejoraron las propiedades mecánicas y de barrera al vapor de agua y al oxígeno de los films de almidón. Estos films se combinaron con films mezcla de PLA:PHBV en bicapas almidón-poliésteres por termocompresión. Las bicapas presentaron una alta capacidad barrera al oxígeno y al vapor de agua comparado con sus respectivas monocapas. La capa de poliéster contribuyó al refuerzo mecánico de la bicapa, aportando alta capacidad de barrera al vapor de agua, mientras que la capa de almidón aportó alta capacidad de barrera al oxígeno a la bicapa. La bicapa con almidón de yuca y goma gelano presentó la mejor adhesión entre capas, con propiedades funcionales adecuadas para el envasado de alimentos. Los ácidos ferúlico, p-cumárico y protocatecuico, con propiedades antimicrobianas y antioxidantes, se incorporaron (2%) en los films mezcla de PLA:PHBV para obtener films activos. Los ácidos fenólicos modificaron positivamente las propiedades de la mezcla de poliésteres, incrementando su módulo de elasticidad y resistencia a la fractura y su capacidad de barrera al vapor de agua y al oxígeno, al tiempo que aumentaron levemente la Tg del material. El ácido protocatecuico provocó los mayores efectos, afectando a la cristalización del PHBV. La liberación de estos compuestos en diferentes simulantes alimentarios (con polaridad alta e intermedia) fue muy limitada en cuanto a velocidad y cantidad liberada, lo que disminuyó la capacidad de las películas para inhibir de forma significativa el crecimiento de Listeria innocua inoculada en medio de cultivo. Estos films, con y sin compuestos activos, se desintegraron en condiciones de compostaje, sin efecto significativo de los ácidos fenólicos. Los films sin activos y con ácido ferúlico se biodegradaron completamente después de 20 días de compostaje, mientras que los films que contenían ácido p-cumárico y protocatecuico lo hicieron en 21 y 26 días, respectivamente. Por lo tanto, ninguno de los ácidos fenólicos incorporados inhibió el proceso de biodegradación, pero se retardó el proceso, dependiendo del grado de retención del compuesto en la matriz polimérica. Los films bicapa biodegradables constituidos por una capa de almidón-gelano y otra de PLA:PHBV, con y sin ácidos fenólicos, se caracterizaron en sus propiedades mecánicas y de barrera al vapor de agua y al oxígeno y se utilizaron para el envasado de carne de cerdo, evaluando su calidad durante el almacenamiento a 5 °C. La presencia de ácidos fenólicos disminuyó el módulo elástico y la tensión de fractura de las bicapas y mejoró su capacidad de barrera al vapor de agua y al oxígeno. Esto último, junto al efecto activo de los ácidos, contribuyó a mejorar la conservación de la carne durante el almacenamiento, reduciendo los niveles de oxidación lipídica, cambios de pH y pérdidas de peso de las muestras envasadas, así como el crecimiento microbiano, especialmente coliformes totales y bacterias ácido-lácticas. Los films bicapa biodegradables con ácidos fenólicos, a base de almidón y poliésteres, se muestran como una estrategia adecuada para obtener materiales de envasado activo, con propiedades funcionales próximas a las de algunos plásticos sintéticos comúnmente utilizados en el envasado de alimentos. Estos materiales pueden alargar la vida útil de los alimentos, mitigando el impacto ambiental de los envases plásticos ya que pueden ser compostados. / [CA] S'han desenvolupat, mitjançant termoprocesat, pel·lícules multicapa biodegradables actives per a l'envasament d'aliments, combinant pel·lícules de midó millorades i d'una mescla de polièsters (PLA-PHBV), amb diferents àcids fenòlics (ferúlic, p-cumàric i protocatecuic). En les pel·lícules midó de iuca o de dacsa es van incorporar gomes d'origen microbià (xantana i gellan) (10%) per a millorar les seues propietats funcionals. Les gomes van millorar les propietats mecàniques i de barrera al vapor d'aigua i a l'oxigen dels films de midó. Aquests films es van combinar amb films mescla de PLA:PHBV en bicapes midó-polièsters per termocompresió. Les bicapes van presentar una alta capacitat barrera a l'oxigen i al vapor d'aigua comparat amb les respectives monocapes. La capa de polièster va contribuir al reforç mecànic de la bicapa, aportant alta capacitat de barrera al vapor d'aigua, mentre que la capa de midó va aportar alta capacitat de barrera a l'oxigen a la bicapa. La bicapa amb midó de iuca i goma gellan va presentar la millor adhesió entre capes, amb propietats funcionals adequades per a l'envasament d'aliments. Els àcids ferúlic, p-cumàric i protocatecuic, amb propietats antimicrobianes i antioxidants, es van incorporar (2%) en els films mescla de PLA:PHBV per a obtindre films actius. Els àcids fenòlics van modificar positivament les propietats de la mescla de polièsters, incrementant el seu mòdul d'elasticitat i resistència a la fractura i la seua capacitat de barrera al vapor d'aigua i a l'oxigen, al mateix temps que van augmentar lleument la Tg del material. L'àcid protocatecuic va provocar els majors efectes, afectant la cristal·lització del PHBV. L'alliberament d'aquests compostos en diferents simulants alimentaris (amb polaritat alta i intermèdia) va ser molt limitada en quant a velocitat i quantitat alliberada, la qual cosa va disminuir la capacitat de les pel·lícules per a inhibir de manera significativa el creixement de Listeria innocua inoculada en medi de cultiu. Aquests films, amb i sense compostos actius, es van desintegrar en condicions de compostatge, sense efecte significatiu dels àcids fenòlics. Els films sense actius i amb àcid ferúlic es biodegradaren completament després de 20 dies de compostatge, mentre que els films que contenien àcid p-cumàric i protocatecuic ho van fer en 21 i 26 dies, respectivament. Per tant, cap dels àcids fenòlics incorporats va inhibir el procés de biodegradació, però es va retardar el procés, depenent del grau de retenció del compost en la matriu polimèrica. Els films bicapa biodegradables constituïts per una capa de midó-gellan i una altra de PLA:PHBV, amb i sense àcids fenòlics es van caracteritzar en les seues propietats mecàniques i de barrera al vapor d'aigua i a l'oxigen i es van utilitzar per a l'envasament de carn de porc, avaluant la qualitat a llarg del emmagatzematge a 5 °C. La presència d'àcids fenòlics va disminuir el mòdul elàstic i la tensió de fractura de les bicapes i va millorar la seua capacitat de barrera al vapor d'aigua i a l'oxigen. Això últim, junt a l'efecte actiu dels àcids, va contribuir a millorar la conservació de la carn durant l'emmagatzematge, reduint els nivells d'oxidació lipídica, canvis de pH i pèrdues de pes de les mostres envasades, així com el creixement microbià, especialment coliformes totals i bacteris àcid-làctics. Els films bicapa biodegradables amb àcids fenòlics, a base de midó i polièsters, es mostren com una estratègia adequada per a obtindre materials d'envasament actiu, amb propietats funcionals pròximes a les d'alguns plàstics sintètics comunament utilitzats en l'envasament d'aliments. Aquests materials poden allargar la vida útil dels aliments, mitigant l'impacte ambiental dels envasos plàstics ja que poden ser compostats. / [EN] Active biodegradable multilayer films have been developed by thermoprocessing for food packaging purposes, combining improved starch films and a blend of polyesters (PLA-PHBV), with different phenolic acids (ferulic, p-coumaric and protocatechuic). Into the cassava or maize starch films, gums of microbial origin (xanthan and gellan) were incorporated (10%) to improve their functional properties. The gums improved the mechanical and barrier properties to water vapor and oxygen of the starch films. These films were combined with PLA:PHBV blend films in starch-polyester bilayers by thermocompression. The bilayers exhibited high barrier capacity to oxygen and water vapor compared to their respective monolayers. The polyester layer contributes to the mechanical reinforcement of the bilayer, providing high water vapor barrier capacity, while the starch layer provided high oxygen barrier capacity to the bilayer. The bilayer with cassava starch and gellan gum showed the best interlayer adhesion, with adequate functional properties for food packaging applications. Ferulic, p-coumaric and protocatechuic acids, with antimicrobial and antioxidant properties, were incorporated (2%) in the PLA: PHBV blend films to obtain active films. Phenolic acids positively modified the properties of the polyester blend, increasing its elastic modulus and resistance to break and its barrier capacity to water vapor and oxygen, while slightly increasing the Tg of the material. Protocatechuic acid caused the greatest effects, affecting the crystallization of PHBV. The release of these compounds in different food simulants (with high and intermediate polarity) was very limited in terms of release rate and released amount, which reduced the ability of the films to significantly inhibit the growth of Listeria innocua inoculated in culture medium. These films, with and without active compounds, disintegrated under composting conditions, without significant effect of phenolic acids. Films without active compounds and with ferulic acid biodegraded completely after 20 days of composting, whereas films containing p-coumaric and protocatechuic acids did so in 21 and 26 days, respectively. Therefore, none of the incorporated phenolic acids inhibited the biodegradation process, but the process was delayed, depending on the degree of retention of the compound in the polymeric matrix. The biodegradable bilayer films with a layer of starch-gellan and another of PLA: PHBV, with and without phenolic acids, were characterized as to their mechanical properties and barrier capacity to water vapor and oxygen and were used for packaging of pork meat whose quality development was analysed throughout storage time at 5 °C. The presence of phenolic acids decreased the elastic modulus and resistance to break of the bilayers and improved their barrier capacity to water vapor and oxygen. The latter, together with the active effect of the acids, contributed to improving the preservation of the meat during storage, reducing the levels of lipid oxidation, changes in pH and weight losses of the packed samples, as well as microbial growth, especially total coliforms and lactic acid bacteria. Biodegradable bilayer films with phenolic acids, based on starch and polyesters, appeared as a suitable strategy to obtain active packaging materials, with functional properties close to those of some synthetic plastics commonly used in food packaging. These materials can extend the shelf-life of foods, mitigating the environmental impact of plastic packaging since they can be composted. / The authors would like to thank the Ministerio de Ciencia e Innovación of Spain, for funding this study through the Project AGL2016-76699-R and PID2019-105207RB-I00, and the predoctoral research grant # BES-2017-082040 / Hernández García, E. (2022). Biodegradable Multilayer Films for Active Food Packaging, Based on Starch and Polyesters with Phenolic Acids [Tesis doctoral]. Universitat Politècnica de València. https://doi.org/10.4995/Thesis/10251/181473 / TESIS / Compendio

The study examined the properties of stalk and cob fibres from recombinant inbred corn lines and their parents, grown at two locations, in a polylactic acid (PLA) matrix. The objectives were to: determine fibre compositions; evaluate the effects of fibres on the functional properties of biocomposites and identify quantitative trait loci (QTLs) and gene markers for fibre performance in biocomposites. Significant Genotype*Location effects were observed. Composites had lower strength (impact, tensile, and flexural) but higher tensile/flexural modulus values than pure PLA. The latter were positively affected by cellulose and hemicellulose but negatively affected by free phenolic levels and 93 fibre QTLs and 62 composite markers were detected. This study identified fibre traits and markers for genes that may be important for the use of corn fibres in biocomposites. / Ontario BioCar Initiative Project funded by Ontario Ministry of Research and Innovation, Agriculture and Agri-Food Canada, The Natural Sciences and Engineering Research Council, The Ontario Ministry of Agriculture, Food and Rural Affairs (OMAFRA) and Ontario Public Sector

No description available.

The present Doctoral Thesis focuses on the investigation, characterization and influence of polyacrylic materials in different scientific and technological disciplines via a detailed computer simulation using the Molecular Dynamics (MD) technique, in conjunction with the very accurate, all-atom Dreiding force-field. The main research concepts and objectives are discussed and analyzed in three separate parts. In the first part, atomistic configurations of two model pressure-sensitive acrylic adhesives (PSAs), the atactic homopolymer poly(n-BA) [poly(n-butyl acrylate)] and the atactic copolymer poly(n-BA-co-AA) [poly(n-butyl acrylate-co-acrylic acid)] in the bulk phase or confined between two selected substrates, glassy silica (SiO2) and metallic α-ferrite (α-Fe), were built and simulated by MD in the NPT statistical ensemble. First, an equilibration cycle consisting of temperature annealings and coolings was followed, in order to generate well-equilibrated configurations of the PSA systems. Detailed results from the atomistic simulations are presented concerning their volumetric behavior, glass transition temperature, conformational, structural, viscoelastic and dynamic properties. Particular emphasis was given to the analysis and characterization of the hydrogen bonds that form in the poly(n-BA-co-AA) system. By analyzing the MD trajectories, poly(n-BA-co-AA) was found to exhibit a higher density than poly(n-BA) by about 7% at all temperatures, to be characterized by smaller-size chains for a given molecular weight (MW), to exhibit significantly slower terminal and segmental dynamics properties, and to be characterized by a glass transition temperature that was approximately 40% higher than that of poly(n-BA). We also examined the type and degree of adsorption of the two acrylic systems on the selected substrates by analyzing the MD results for the local mass density as a function of distance from the solid plane and the distribution of adsorbed chain segments in train, loop, and tail conformations, and by computing the work of adhesion at the two substrates. The results revealed a stronger adsorption for both acrylics on the SiO2 surface due to highly attractive interactions between polymer molecules and substrate atoms, and as a consequence a higher value for the work of adhesion compared to that on the α-Fe surface. Furthermore, we have developed a generalized non-equilibrium molecular dynamics (NEMD) algorithm to simulate the mechanical response of the two adhesives under a uniaxial stretching deformation. In the second part of the Thesis, results have been obtained from a hierarchical simulation methodology that led to the prediction of the thermodynamic, conformational, structural, dynamic and mechanical properties of two polymer nanocomposites based on syndiotactic poly(methyl methacrylate) or sPMMA. The first was reinforced with uniformly dispersed graphene sheets and the second with fullerene particles. How graphene functionalization affects the elastic constants of the resulting nanocomposite has also been examined. The phase behavior of the nanocomposite (in particular as we varied the relative size between the sPMMA chains and the diameter of fullerene molecules) has also been studied as a function of fullerene volume fraction. The simulation strategy entailed three steps: 1) Generation of an initial structure, which was then subjected to potential energy minimization and detailed molecular dynamics (MD) simulations at T = 500K and P = 1atm to obtain well relaxed melt configurations of the nanocomposite. 2) Gradual cooling of selected configurations down to room temperature to obtain a good number of structures representative of the glassy phase of the polymer nanocomposite. 3) Molecular mechanics (MM) calculations of its mechanical properties following the method originally proposed by Theodorou and Suter. By analyzing the results under constant temperature and pressure, all nanocomposite systems were found to exhibit slower terminal and segmental relaxation dynamics than the pure polymer matrices. The addition of a small fraction of graphene sheets led in all cases to the enhancement of the elastic constants; this was significantly more pronounced in the case of functionalized graphene sheets. We further mention that, for all polymer/fullerene nanocomposites addressed here, no phase separation or variation of polymer chain dimensions was observed as a function of fullerene size and/or fullerene volume fraction. In the third part of the Thesis, and motivated by the use of acrylic polymers for the design of membranes with aligned carbon nanotubes (CNTs) for several separation technologies (such as water desalination and wastewater treatment), we report results from a detailed computer simulation study for the nano-sorption and mobility of four different small molecules (water, tyrosol, vanillic acid, and p-coumaric acid) inside smooth single-wall CNTs (SWCNTs). Most of the results have been obtained with the molecular dynamics (MD) method, but especially for the most narrow of the CNTs considered, the results for water molecule were further confirmed through an additional Grand Canonical (μVT) Monte Carlo (GCMC) simulation using a value for the water chemical potential μ pre-computed with the particle deletion method. Issues addressed in the Thesis include molecular packing and ordering inside the nanotube for the four molecules, average number of sorbed molecules per unit length of the tube, and mean residence time and effective axial diffusivities, all as a function of tube diameter and tube length. In all cases, a strong dependence of the results on carbon nanotube diameter was observed, especially in the way the different molecules are packed and organized inside the CNT. For water for which predictions of properties such as local structure and packing were computed with both methods (MD and GCMC), the two sets of results were found to be fully self-consistent for all types of SWCNTs considered. Water diffusivity inside the CNT (although, strongly dependent on the CNT diameter) was computed with two different methods, both of which gave identical results. For large enough CNT diameters (larger than about 13 Å), this was found to be higher than the corresponding experimental value in the bulk by about 55%. Surprisingly enough, for the rest of the (phenolic) molecules simulated in this Thesis, the simulations revealed no signs of mobility inside nanotubes with a diameter smaller than the (20, 20) tube. This has been attributed to strong phenyl-phenyl attractive interactions, also to favorable interactions of these molecules with the CNT walls, which cause them to form highly ordered, very stable structures inside the nanotube, especially under strong confinement. The interaction, in particular, of the methyl group (present in tyrosol, vanillic acid, and p-coumaric acid) with the CNT walls seems to play a key role in all these compounds causing them to remain practically immobile inside nanotubes characterized by diameters smaller than about 26 Å. It was only for larger-diameter CNTs that tyrosol, vanillic acid, and p-coumaric acid were observed to demonstrate appreciable mobility. / Η παρούσα Διδακτορική Διατριβή εστιάζει στη μελέτη της σχέσης μεταξύ δομής και μακροσκοπικών φυσικών ιδιοτήτων υλικών από πολυακρυλικά μέσω μίας λεπτομερούς προσομοίωσης στον υπολογιστή με τη μέθοδο της Μοριακής Δυναμικής (ΜΔ), σε συνδυασμό με ένα πολύ επακριβές πεδίο δυνάμεων (το Dreiding) σε ατομιστική λεπτομέρεια. Οι κύριες ερευνητικές έννοιες καθώς και οι στόχοι συζητιούνται και αναλύονται σε τρία ξεχωριστά μέρη. Στο πρώτο μέρος, ατομιστικές απεικονίσεις δύο προτύπων πίεσο-ευαίσθητων συγκολλητικών υλικών (acrylic pressure sensitive adhesives ή PSAs), του ατακτικού πολυ-βουτυλικού-ακρυλικού εστέρα (poly(n-BA)) και του συμπολυμερούς του με ακρυλικό οξύ (poly(n-BA-co-AA)), τόσο μακριά όσο και κοντά σε υποστρώματα σίλικας (SiO2) και α-φερρίτη (α-Fe), μελετήθηκαν στη βάση ενός φάσματος ιδιοτήτων (θερμοδυναμικές, δομικές, ιξωδοελαστικές, δυναμικές, και συγκολλητικές), όπως και η μηχανική τους απόκριση υπό συνθήκες μονοαξονικής εκτατικής παραμόρφωσης. Στο δεύτερο μέρος παρουσιάζονται τα αποτελέσματα που εξήχθησαν από μία ιεραρχική μεθοδολογία προσομοίωσης που οδήγησε στην πρόβλεψη της φασικής συμπεριφοράς και των μηχανικών ιδιοτήτων νανοσύνθετων πολυμερικών υλικών (polymer nanocomposites ή PNCs) βασισμένων στο συνδιοτατκτικό πολυ-μεθακρυλικό μεθυλεστέρα (syndiotactic poly(methyl methacrylate) ή sPMMA), ενισχυμένο με ομοιόμορφα διεσπαρμένα φύλλα γραφενίου (graphene sheets) ή σωματίδια φουλερενίου (fullerene particles). Στο τρίτο μέρος, υποκινούμενοι από τη χρήση των ακρυλικών πολυμερών στο σχεδιασμό μεμβρανών με ενσωματωμένους ευθυγραμμισμένους νανοσωλήνες άνθρακα (ΝΑ, carbon nanotubes ή CNTs) σε διάφορες τεχνολογίες διαχωρισμού μορίων (με έμφαση στον καθαρισμό του νερού), παρουσιάζουμε αποτελέσματα από προσομοιώσεις, για τη νανο-ρόφηση και την κινητικότητα τεσσάρων διαφορετικών μικρών μορίων (water, tyrosol, vanilic acid, και p-coumaric acid) στο εσωτερικό λείων μονο-στρωματικών ΝΑ (single-wall CNTs ή SWCNTs). Τα θέματα που εξετάζονται περιλαμβάνουν τη μοριακή διευθέτηση και τη διάταξη στο εσωτερικό Ν.Α. των τεσσάρων μορίων, το μέσο χρόνο παραμονής τους, καθώς και τους αξονικούς συντελεστές διάχυσής του, συναρτήσει της διαμέτρου και του μήκους των ΝΑ.