Development of waterborne polyurethane-ureas added with plant extracts: Study of different incorporation routes and their influence on particle size, thermal, mechanical and antibacterial properties

Polyurethane-ureas are a versatile family of polymers which can be employed in a wide range of applications. Among them, waterborne polyurethane-urea (WBPUU) dispersions are gaining relevance in the field of environmentally-friendly products since their productive process adopts green synthesis routes, avoiding the use of organic solvents. Furthermore, their waterborne character can be exploited to incorporate several water compatible ingredients able to confer functional properties to the final materials. Among them, plant extracts, which are known to have relevant bioactivities, can be viewed as interesting candidates. Therefore, in this work, two extracts known to present antimicrobial activity (Melissa officinalis L. and Salvia officinalis L.) were obtained by the infusion method and incorporated into the WBPUU (1, 3 and 5 wt%) following different incorporation routes comprising its adding during different phases of the productive process (post-, in-situ and pre- methods). Thereafter films were prepared by solvent-casting and characterized from the viewpoint of physicochemical, thermal, mechanical, thermomechanical and antibacterial properties and morphologically. The studied incorporation routes resulted in different intercalation mechanisms that varied from extract positioned among the polyurethane-urea nanoparticles (post-method) to extract partially embedded inside them (in-situ and pre-methods), which produced stiffening or flexibilizing effects in the produced films, enhancing in general the antimicrobial characteristics of films after 4 days of incubation comparing with base WBPUU, especially when the extract is embedded.Financial support from the Basque Government (IT-776-13), the Spanish Ministry of Economy and Competitiveness (MINECO) (MAT2016-76294-R), POCI-01-0145-FEDER-006984 (LA LSRE-LCM) funded by ERDF through POCI-COMPETE2020 and FCT and NORTE-01-0145-FEDER-000006, funded by NORTE 2020, under PT2020 through ERDF is gratefully acknowledged. We also wish to acknowledge the “Macrobehaviour- Mesostructure-Nanotechnology” SGIker units from the University of the Basque Country, for their technical support. A.S-E thanks the University of the Basque Country for Ph.D. grant (PIF/UPV/12/201).Financial support from the Basque Government (IT-776-13), the Spanish Ministry of Economy and Competitiveness (MINECO) (MAT2016-76294-R), POCI-01-0145-FEDER-006984 (LA LSRE-LCM) funded by ERDF through POCI-COMPETE2020 and FCT and NORTE- 01-0145-FEDER-000006, funded by NORTE 2020, under PT2020 through ERDF is gratefully acknowledged. We also wish to acknowledge the “Macrobehaviour- Mesostructure-Nanotechnology” SGIker units from the University of the Basque Country, for their technical support. A.S-E thanks the University of the Basque Country for Ph.D. grant (PIF/UPV/12/201).info:eu-repo/semantics/publishedVersio

Effect of hot calendering on physical properties and water vapor transfer resistance of bacterial cellulose films

This work investigates the effect of hot calendering on bacterial cellulose (BC) films properties, aiming the achievement of good transparency and barrier property. A comparison was made using vegetal cellulose (VC) films on a similar basis weight of around 40 g.m-2. The optical-structural, mechanical and barrier property of BC films were studied and compared with those of highly beaten VC films. The Youngs moduli and tensile index of the BC films are much higher than those obtained for VC (14.5 16.2 GPa vs 10.8 8.7 GPa and 146.7 64.8 N.m.g-1 vs 82.8 40.5 N.m.g-1), respectively. Calendering increased significantly the transparency of BC films from 53.0 % to 73.0 %. The effect of BC ozonation was also studied. Oxidation with ozone somewhat enhanced the brightness and transparency of the BC films, but at the expenses of slightly lower mechanical properties. BC films exhibited a low water vapor transfer rate, when compared to VC films and this property decreased by around 70 % following calendering, for all films tested. These results show that calendering could be used as a process to obtain films suitable for food packaging applications, where transparency, good mechanical performance and barrier properties are important. The BC films obtained herein are valuable products that could be a good alternative to the highly used plastics in this industry.The authors thank FCT (Fundação para a Ciência e Tecnologia) and FEDER (Fundo Europeu de Desenvolvimento Regional) for the financial support of the project FCT PTDC/AGR-FOR/3090/2012— FCOMP-01-0124-FEDER-027948 and the awarding of a research grant for Vera Costa

On the use of nanocellulose as reinforcement in polymer matrix composites

AbstractNanocellulose is often being regarded as the next generation renewable reinforcement for the production of high performance biocomposites. This feature article reviews the various nanocellulose reinforced polymer composites reported in literature and discusses the potential of nanocellulose as reinforcement for the production of renewable high performance polymer nanocomposites. The theoretical and experimentally determined tensile properties of nanocellulose are also reviewed. In addition to this, the reinforcing ability of BC and NFC is juxtaposed. In order to analyse the various cellulose-reinforced polymer nanocomposites reported in literature, Cox–Krenchel and rule-of-mixture models have been used to elucidate the potential of nanocellulose in composite applications. There may be potential for improvement since the tensile modulus and strength of most cellulose nanocomposites reported in literature scale linearly with the tensile modulus and strength of the cellulose nanopaper structures. Better dispersion of individual cellulose nanofibres in the polymer matrix may improve composite properties

A common strategy to extracting cellulose nanoentities from different plants

cited By 31International audienceIn order to obtain cellulose nanoentities like nanofibres (CNF) and nanocrystals (CNC) from sisal (S), hemp (He) and flax (F) fibres, a new succession of specific chemical treatments including extractives (E), prealkalization (PA), alkalization (A), acetylation (Ac) and acid hydrolysis (H) treatments have been developed. Cellulose nanoentities obtained have been characterized by different techniques. FTIR spectra confirmed the removal of non-cellulosic components after chemical treatments. XRD results showed that all samples exhibited cellulose I crystalline structure and the crystallinity index of cellulose nanoentities was increased about 30% relative to raw fibres owing to removal of non-cellulosic components. The thermal stability of samples decreased after using an acid medium. AFM images confirmed that cellulose nanofibres and nanocrystals were obtained. © 2014 Elsevier B.V

Pineapple agroindustrial residues for the production of high value bacterial cellulose with different morphologies

cited By 8International audienceBacterial cellulose (BC) with different morphologies was biosynthesized by Gluconacetobacter medellinensis strain under static and dynamic culture conditions using sugar cane juice and pineapple residues as sources of carbon and other nutrients. Hestrin and Schramm's standard culture medium was used as reference. The fermentation condition and resulting yield, physico-chemical properties, and morphology relationships of obtained cellulose were analyzed. Pineapple agroindustrial residues can be envisaged as an inexpensive and sustainable alternative resource for the production of different BC morphologies. © 2014 Wiley Periodicals, Inc

Copolymers based on epoxidized soy bean oil and diglycidyl ether of bisphenol a: Relation between morphology and fracture behavior

Epoxidized soybean oil (ESO) was proved to be a good alternative to partially replace a synthetic commercial epoxy resin in a formulation to obtain thermosetting polymer, contributing to transform a vegetable oil into a higher added value product. This work focuses on the study of the fracture behavior of copolymers based on anhydride-cured epoxy systems with different contents of ESO as a replacement for the synthetic resin. It was found that fracture toughness was greatly improved when replacing diglycidyl ether of bisphenol A (DGEBA) by ESO, being the critical stress intensity factor (KIC) 1.067 MPam1/2 for cured ESO and 0.557 MPam1/2 for cured DGEBA. The better performance of ESO networks was ascribed to its higher ability to attain plastic deformation. Moreover, for DGEBA-ESO systems, the morphologies generated during the curing process were also considered to account for the observed results.Fil: Altuna, Facundo Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Pettarin, Valeria. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Martin, L.. Universidad del País Vasco; EspañaFil: Retegi, A.. Universidad del País Vasco; EspañaFil: Mondragón, I.. Universidad del País Vasco; EspañaFil: Ruseckaite, Roxana Alejandra. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Stefani, Pablo Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; Argentin

Sustainable optically transparent composites based on epoxidized soy-bean oil (ESO) matrix and high contents of bacterial cellulose (BC)

Production of transparent composites from totally renewable resources with extraordinary potential for different applications can be made possible using cellulose. Composites of epoxidized soybean oil (ESO)/bacterial cellulose (BC) nanofibers have been prepared with high fiber content. Due to the nano-order scale network-like structure of BC nanofibers, composite films present high transparency even at high BC content. Transparency of films has been analyzed by UV-visible spectroscopy observing that only 15% of matrix transmittance is lost in the nanocomposites. ESO/BC composites show better mechanical properties with increasing BC content. Composites combine high stiffness and good ductility due to the incorporation of BC network structure in ESO matrix. © 2011 Springer Science+Business Media B.V.Fil: Retegi, A.. Universidad del País Vasco; EspañaFil: Algar, I.. Universidad del País Vasco; EspañaFil: Martin, L.. Universidad del País Vasco; EspañaFil: Altuna, Facundo Ignacio. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Stefani, Pablo Marcelo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Mar del Plata. Instituto de Investigaciones en Ciencia y Tecnología de Materiales. Universidad Nacional de Mar del Plata. Facultad de Ingeniería. Instituto de Investigaciones en Ciencia y Tecnología de Materiales; ArgentinaFil: Zuluaga, R.. Universidad Pontificia Bolivariana; ColombiaFil: Gañán, P.. Universidad Pontificia Bolivariana; ColombiaFil: Mondragon, I.. Universidad del País Vasco; Españ

Bacterial nanocellulose production from naphthalene

Polycyclic aromatic compounds (PAHs) are toxic compounds that are released in the environment as a consequence of industrial activities. The restoration of PAH-polluted sites considers the use of bacteria capable of degrading aromatic compounds to carbon dioxide and water. Here we characterize a new Xanthobacteraceae strain, Starkeya sp. strain N1B, previously isolated during enrichment under microaerophilic conditions, which is capable of using naphthalene crystals as the sole carbon source. The strain produced a structured biofilm when grown on naphthalene crystals, which had the shape of a half-sphere organized over the crystal. Scanning electron microscopy (SEM) and GC-MS analysis indicated that the biofilm was essentially made of cellulose, composed of several micron-long nanofibrils of 60 nm diameter. A cellulosic biofilm was also formed when the cells grew with glucose as the carbon source. Fourier transformed infrared spectroscopy (FTIR) confirmed that the polymer was type I cellulose in both cases, although the crystallinity of the material greatly depended on the carbon source used for growth. Using genome mining and mutant analysis, we identified the genetic complements required for the transformation of naphthalene into cellulose, which seemed to have been successively acquired through horizontal gene transfer. The capacity to develop the biofilm around the crystal was found to be dispensable for growth when naphthalene was used as the carbon source, suggesting that the function of this structure is more intricate than initially thought. This is the first example of the use of toxic aromatic hydrocarbons as the carbon source for bacterial cellulose production. Application of this capacity would allow the remediation of a PAH into such a value-added polymer with multiple biotechnological usages.This work was supported by the European Regional Development Fund FEDER and grants from the Spanish Ministry of Economy and Competitiveness (BIO2017‐82242‐R).Peer Reviewe