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The use of biodegradable polymers in the plastics industry has been increasing in recent years. The study of the chemical, physical, thermal, and mechanical properties of films based on biodegradable components is of interest to technologists because these properties determine their applicability for food packaging. In this work, films based on natural polymers such as linseed mucilage (LM) and chitosan (CH), as well as poly(acrylic acid) (PAA) were obtained through the casting method and using V‐50 as the initiator. The films were characterized through Fourier Transform Infrared spectroscopy, and thermogravimetric analysis, and their water absorption and swelling capacity, and thermal and mechanical properties were determined. Homogenous flexible, translucid, amber‐colored films, with low absorption and solubility in water were obtained. It was demonstrated through Fourier Transform Infrared analysis the chemical interaction between C–H, CO, and C–O chemical groups of LM, CH, and PAA. In addition, films showed high resistance to thermal decomposition between 125 and 425°C. The mechanical tests of tension allowed the composition of LM in the film, the behavior variates between a plastic and/or elastic material and with tensile strength (Rm) values between 10.8 and 16.4 MPa and elastic modulus (E) values between 56.2 and 169.2 GPa, we observed that at higher quantities of LM and thickness, both E and Rm tend to increase, while %EL decreases. This led us to conclude that the material transitioned from ductile and malleable to rigid and brittle. The films obtained with different ratios of LM/CH/PAA may exhibit a semi‐interpenetrating polymeric networking type morphology. Highlights: Thermal and mechanical properties are of interest in food packaging materials.Water absorption can impact the packaged food.Films can be processed on existing machines for conventional plastics.Some conventional plastics could be replaced by these biodegradable films.Biodegradable films are of great interest to the industry of food packaging. [ABSTRACT FROM AUTHOR]

Polymer biocompositions of poly(3-hydroxybutyrate) (P3HB) and linear polyurethanes (PU) with aromatic rings were produced by melt-blending at different P3HB/PU weight ratios (100/0, 95/5, 90/10, and 85/15). Polyurethanes have been prepared with 4,4′-diphenylmethane diisocyanate and polyethylene glycols with molar masses of 400 g/mol (PU400), 1000g/mol (PU1000), and 1500 g/mol (PU1500). The compatibility and morphology of the obtained polymer blends were determined by infrared spectroscopy (FTIR), scanning electron microscopy (SEM), and differential scanning calorimetry (DSC). The effect of the polyurethane content in the biocompositions on their thermal stability and mechanical properties was investigated and compared with those of the native P3HB. It was shown that increasing the PU content in P3HB-PU compositions to 10 wt.% leads to an improvement in the mentioned properties. The obtained results demonstrated that the thermal stability and mechanical properties of P3HB were improved, particularly in terms of increasing the degradation temperature, reducing hardness, and increasing impact strength. The best thermal and mechanical properties were shown by the P3HB-PU polymer compositions containing 10 wt.% of polyurethane modifiers, especially PU1000, which was also confirmed by the morphology analysis of these biocompositions. The presence of polyurethanes in the resulting polymer biocomposites decreases their glass transition temperatures, i.e., makes the materials more flexible. The resulting polymer biocompositions have suitable mechanical properties and thermal properties within the processing conditions for the predicted application as biodegradable, short-lived products for agriculture. [ABSTRACT FROM AUTHOR]

Tamarind seed polysaccharides (TSPs), in conjunction with alkali nitrate, specifically lithium nitrate (LiNO3), were utilized at various concentrations. The aforementioned precursor was dispersed in an aqueous solvent medium using the solution casting route to synthesize thin film polymer electrolytes based on TSP:LiNO3. A comprehensive characterization, incorporating X-ray diffraction (XRD), Fourier transform infrared (FT-IR), differential scanning calorimetry (DSC), impedance analysis, and linear sweep voltammetry (LSV), was conducted to elucidate key properties, including crystallinity state (crystalline or amorphous), vibrational band shifts, endothermic point characteristics, ionic conductivity, mobility (both cationic and anionic), diffusion coefficients (both cation and anion), transference number, and electrochemical stability. The investigation revealed that the structural properties of the polymer electrolytes are notably influenced by the varying concentrations of LiNO3 in the polymer host. The maximum ionic conductivity was found to be 1.41 × 10−3 S cm−1 for the composition of 750 mg TSP:250 mg LiNO3. The electrochemical stability value and transference number of the prepared TSP:LiNO3 are 4 V and 0.68, respectively. Primary lithium-ion cell has been constructed for highest conducting sample which delivered an open circuit voltage of 1.5 V, and also, the discharge profile with 1 MΩ load has been studied. [ABSTRACT FROM AUTHOR]

Medicated jellies are widely used by a large part of patients, especially by people with swallowing difficulties. Preformulation studies play an essential role in the development of new pharmaceutical formulations. The present study aimed to formulate and evaluate medicated jellies containing perphenazine, an antipsychotic drug from the group of phenothiazine compounds used to treat schizophrenia and other mental disorders. Typical gelling agents such as sodium alginate (Alg), gelatine (Gel), and pectin (Pec) were used to develop the medicated jellies. In addition to the biopolymers, components such as benzoic acid (BenzAc), citric acid (CitAc), sodium citrate (NaCit), sorbitol (Sorb) and xylitol (Xyl) were also used. Before preparing the jellies, the moist binary mixture between each component of the jelly and the active substance was analysed to investigate the compatibility of the substances. The active substance, moist binary mixture, and medicated jellies were analysed by FTIR_UATR spectroscopy, UV-Vis spectroscopy and thermogravimetry. [ABSTRACT FROM AUTHOR]

This study aimed to determine the effects of the ozone treatment of film-forming solutions (FFSs) containing whey protein concentrate (WPC) and gelatine on biopolymer films' physical, mechanical, and thermal properties. Film samples were produced from a FFS that was ozone-treated at 0 (control), 5, 10, and 30 min. Ozone treatment caused an increase in the pH values of the FFS, whereas the zeta potential remained negative. The films became lighter in colour, slightly greenish, and more opaque with longer ozonation times. The control sample showed the highest thermogravimetric weight loss (92.15%). The weight loss of the samples decreased with increasing ozone treatment time. The application of ozone treatment on the FFS enhanced the films' mechanical properties. Increased ozone treatment time improved the film samples' tensile strength, elongation at break, and toughness values. In conclusion, the results of this study demonstrate that the ozone treatment of FFS containing whey protein concentrate and gelatine can significantly enhance the physical, mechanical, and thermal properties of biopolymer films. These results highlight the potential of ozone treatment as a viable method for improving the performance and quality of biopolymer films used in food packaging, offering promising advantages for sustainable and environmentally friendly packaging solutions. [ABSTRACT FROM AUTHOR]

Due to the growing interest in biopolymers, biosynthesizable and biodegradable polymers currently occupy a special place. Unfortunately, the properties of native biopolymers make them not good enough for use as substitutes for conventional polymers. Therefore, attempts are being made to modify their properties. In this work, in order to improve the properties of the poly(3-hydroxybutyrate) (P3HB) biopolymer, linear aliphatic polyurethane (PU) based on 1,4-butanediol (BD) and hexamethylene 1,6-diisocyanate (HDI) was used. The conducted studies on the effect of the amount of PU used (5, 10, 15 and 20 m/m%) showed an improvement in the thermal properties of the prepared polymer blends. As part of the tested mechanical properties of the new polymer blends, we noted the desired increase in the tensile strength, and the impact strength showed a decrease in hardness, in particular at the presence of 5 m/m% PU. Therefore, for further improvement, hybrid nanobiocomposites with 5 m/m% PU and organically modified montmorillonite (MMT) (Cloisite 30®B) were produced. The nanoadditive was used in a typical amount of 1–3 m/m%. It was found that the obtained nanobiocomposites containing the smallest amount of nanofillers, i.e., 1 m/m% Cloisite®30B, exhibited the best mechanical and thermal properties. [ABSTRACT FROM AUTHOR]

Natural and biodegradable polymers with pH-responsive properties, such as alginate and chitosan, are widely exploited for drug delivery applications, most notably in the form of biocompatible microspheres. In addition, thermo-responsive poly(N-isopropyl-acrylamide) (PNIPAM) is often added to biomedical delivery systems due to its lower critical solution temperature close to human physiological conditions. In this work, multi-responsive microspheres (MRMs) consisting of a hydrogel matrix made of alginate, chitosan, and PNIPAM were successfully prepared by extrusion dripping and proposed as delivery system for Ozoile (Stable Ozonides) derived from biological olive oil. Ozoile acts as a biological inducer, regulating the main metabolic pathways and stimulating the endogenous defence system. The MRMs containing Ozoile were prepared from alginate/NIPAM emulsions integrating the lipophilic bioactive principle. The MRMs were further optimised with a chitosan coating to improve their stability and control the degradation behaviour of the hydrogel matrix, with subsequent release of Ozoile. Results in terms of chemical composition from Fourier transform infrared (FTIR) spectroscopy, thermo-responsive properties from differential scanning calorimetry (DSC) analysis, swelling and degradation behaviour were used to establish the potential use of the MRMs for the therapeutic release of Ozoile at specific inflammatory sites. [ABSTRACT FROM AUTHOR]

The current research is devoted to the investigation of the plasticization of polyhydroxybutyrate (PHB) and polyhydroxybutyrate-co-hydroxyvalerate (PHBV) with triethyl citrate (TEC). Three different PHB or PHBV-based systems with 10, 20, and 30 wt.% of TEC were prepared by two-roll milling. The effect of TEC on the rheological, thermal, mechanical, and calorimetric properties of the developed compression-molded PHB and PHBV-based systems was determined. It was revealed that the addition of TEC significantly influenced the melting behavior of both polyhydroxyalkanoates (PHA), reducing their melting temperatures and decreasing viscosities. It was also revealed that all the investigated systems demonstrated less than 2% weight loss until 200 °C and rapid degradation did not occur until 240–260 °C in an oxidative environment. Apart from this, a remarkable increase (ca 2.5 times) in ultimate tensile deformation εB was observed by increasing the amount of TEC in either PHB or PHBV. A concomitant, considerable drop in ultimate strength σB and modulus of elasticity E was observed. Comparatively, the plasticization efficiency of TEC was greater in the case of PHBV. [ABSTRACT FROM AUTHOR]

Highly methylated apple pectin (HMAP) and pork gelatin (PGEL) have been proposed as gelling agents for pumpkin purée-based films. Therefore, this research aimed to develop and evaluate the physiochemical properties of composite vegetable films. Granulometric analysis of film-forming solutions showed a bimodal particle size distribution, with two peaks near 25 µm and close to 100 µm in the volume distribution. The diameter D4.3, which is very sensitive to the presence of large particles, was only about 80 µm. Taking into account the possibility of creating a polymer matrix from pumpkin purée, its chemical characteristic was determined. The content of water-soluble pectin was about 0.2 g/100 g fresh mass, starch at the level of 5.5 g/100 g fresh mass, and protein at the level of about 1.4 g/100 g fresh mass. Glucose, fructose, and sucrose, the content of which ranged from about 1 to 1.4 g/100 g fresh mass, were responsible for the plasticizing effect of the purée. All of the tested composite films, based on selected hydrocolloids with the addition of pumpkin purée, were characterized by good mechanical strength, and the obtained parameters ranged from about 7 to over 10 MPa. Differential scanning calorimetry (DSC) analysis determined that the gelatin melting point ranged from over 57 to about 67 °C, depending on the hydrocolloid concentration. The modulated differential scanning calorimetry (MDSC) analysis results exhibited remarkably low glass transition temperature (Tg) values, ranging from −34.6 to −46.5 °C. These materials are not in a glassy state at room temperature (~25 °C). It was shown that the character of the pure components affected the phenomenon of water diffusion in the tested films, depending on the humidity of the surrounding environment. Gelatin-based films were more sensitive to water vapor than pectin ones, resulting in higher water uptake over time. The nature of the changes in water content as a function of its activity indicates that composite gelatin films, with the addition of pumpkin purée, are characterized by a greater ability to adsorb moisture from the surrounding environment compared to pectin films. In addition, it was observed that the nature of the changes in water vapor adsorption in the case of protein films is different in the first hours of adsorption than in the case of pectin films, and changes significantly after 10 h of the film staying in an environment with relative humidity RH = 75.3%. The obtained results showed that pumpkin purée is a valuable plant material, which can form continuous films with the addition of gelling agents; however, practical application as edible sheets or wraps for food products needs to be preceded with additional research on its stability and interactions between films and food ingredients. [ABSTRACT FROM AUTHOR]

Chitosan is one of the most commonly employed natural polymers for biomedical applications. However, in order to obtain stable chitosan biomaterials with appropriate strength properties, it is necessary to subject it to crosslinking or stabilization. Composites based on chitosan and bioglass were prepared using the lyophilization method. In the experimental design, six different methods were used to obtain stable, porous chitosan/bioglass biocomposite materials. This study compared the crosslinking/stabilization of chitosan/bioglass composites with ethanol, thermal dehydration, sodium tripolyphosphate, vanillin, genipin, and sodium β-glycerophosphate. The physicochemical, mechanical, and biological properties of the obtained materials were compared. The results showed that all the selected crosslinking methods allow the production of stable, non-cytotoxic porous composites of chitosan/bioglass. The composite with genipin stood out with the best of the compared properties, taking into account biological and mechanical characteristics. The composite stabilized with ethanol is distinct in terms of its thermal properties and swelling stability, and it also promotes cell proliferation. Regarding the specific surface area, the highest value exposes the composite stabilized by the thermal dehydration method. [ABSTRACT FROM AUTHOR]

Various environmental concerns motivate scientists and researchers to look out for unique new materials in science and technology. In order to address the demand for polymeric materials with partial biodegradability, the usage of lignocellulosic fibre in the polymer matrix has risen. Lignocellulosic fibres are a cheap, easily renewable resource that is readily available in all regions. Cellulosic plant fibres also have a plethora of possibilities for use in polymer reinforcement because of their properties. Many researchers put their effort into developing a natural polymer with better mechanical properties and thermal stability using nanotechnology and the use of natural polymers to make its composites with lignocellulosic fibres. This study provides a review of the biodegradable composite market, processing methods, matrix-reinforcement phases, morphology, and characteristic improvements. In addition, it provides a concise summary of the findings of significant research on natural fibre polymer composites (NFRCs) that have been published. Indeed, a noticeably brief discussion is provided on the significant issues faced during composite extraction as well as the challenges encountered during the machining. Recent developments in the study of lignocellulosic fibre composites or NFRCs have demonstrated their enormous potential as structural elements in vehicles, aerospace structures, buildings, ballistics, soundproofing, and other structures. [ABSTRACT FROM AUTHOR]

In this work, new furan-based poly(ester amide)s of various compositions were synthesised by the melt polycondensation method. The chemical structure and composition were determined by nuclear magnetic resonance spectroscopy (1H NMR) and Fourier transform infrared (FTIR) analyses. The optical properties were studied by UV-Vis spectroscopy. The thermal properties were investigated by means of differential scanning calorimetry (DSC). The thermo-oxidative stability of PEAs was also tested. Additionally, the free volume by positron annihilation lifetime spectroscopy (PALS) technique and mechanical properties were examined. It was found that the incorporation of poly(propylene furanamide) (PPAF) units significantly affects the thermal and mechanical properties of co-polymers based on poly(hexylene 2,5-furandicarboxylate) (PHF). Depending on the composition, both semi-crystalline and amorphous co-polymers were obtained. Moreover, the values of the free volume radius (R) and the free volume fractions (fv) were strongly affected by the mole fraction of PPAF units.

Despite the fact that amino cellulose (AC) is biodegradable, biocompatible, and has excellent film-forming properties, AC films have poor mechanical properties and are not thermally stable. An AC-based composite film prepared from AC and curcumin-stearylamine based benzoxazine (C-st) is reported in order to improve its performance and promote its application. As starting materials, C-st and AC were used to produce a C-st/AC composite film possessing a synergistic property through chemical cross-linking and hydrogen bonds. Two salient features with respect to the curing behavior were obtained. Firstly, the onset of curing was reduced to 163 °C when the benzoxazine monomer was synthesized from fully bio-based precursors (such as curcumin and stearylamine). Secondly, a synergistic effect in curing behavior was obtained by mixing C-st with AC. As a result of tensile tests and thermal analysis, the poly(C-st) benefited the composite films with pronounced mechanical and thermal properties, even at elevated temperatures. There was a 2.5-fold increase in tensile strength compared to the AC film, indicating that the composite films have the potential to be used for functional purposes. These poly(C-st)/AC films with improved mechanical and thermal properties have the ability to replace naturally occurring polymer films in film-related applications. [ABSTRACT FROM AUTHOR]

Toughening efficiency of poly(ethylene-n-butylene-acrylate-co-glycidyl methacrylate) (EBA-GMA) in poly(lactic acid) (PLA) matrix has been found to significantly increase at elevated blending temperature. In the case of PLA/EBA-GMA blends having 10.0 or 12.5 wt% EBA-GMA contents, the accelerated PLA degradation at raised processing temperature resulted in reduced mechanical performance. At 15.0 wt% EBA-GMA ratio, however, increased elongation and by 250% improved notched Izod impact strength was achieved when the blending temperature was raised from 240 to 260 °C. This beneficial effect is attributed to the accelerated compatibilization reactions between the components in the presence of shortchain PLA molecules, which allow the rapid formation of a toughening enhancer interphase (TEI) during melt processing. As a result, the brittle-ductile transition can be reached at lower elastomer content than expected. Decreased melt flow index (MFI) values besides stabilized blend morphology indicated efficient PLA--EBA-GMA compatibilization at elevated processing temperature. Accordingly, enhanced nucleation ability of the PLA/EBA-GMA interphase and hindered chain crystallization of PLA were found by differential scanning calorimetry (DSC) analyses. In association with the intensified compatibilization reactions cross-linking of the terpolymer was also revealed using the thermally stimulated depolarization current (TSDC) technique. [ABSTRACT FROM AUTHOR]

With the increase in environmental pollution, studies on the use of sustainable resources are increasing day by day. For this purpose, the use of natural fiber-reinforced polymer composites is encouraged in many areas such as automotive, transportation, construction, and home textiles. However, they are flammable and therefore seriously threaten the safety of people and property. Various flame retardant additives have been used to improve the flame retardancy properties of these composites. In this study, silicon dioxide (SD) and zinc borate (ZB) microparticles in different weight percentages (3, 5, 7, and 10%) were reinforced to give flame retardant properties to jute-epoxy composites. In addition, composites containing both SD and ZB microparticles were produced and they were labeled as HB. Then, thermal conductivity, flammability, water absorption, and mechanical properties of these composites were investigated. The burning rate of the composites decreased as the amount of microparticle increased. 5ZB5SD, including %5 SD and %5 SD microparticles, showed 36.60% less burning rate than the neat jute-epoxy composite. 5ZB showed 10.84% higher tensile strength than the neat juteepoxy. The impact strength of the specimens increased with the increase in the filling ratio, and 5ZB5SD showed approximately 2.50 times the impact strength of the jute-epoxy composite. [ABSTRACT FROM AUTHOR]

In the past few years, a new passion for the growth of biodegradable polymers based on elements derived from natural sources has been getting much attention. Natural fiber-based polymer matrix composites offer weight loss, reduction in cost and carbon dioxide emission, and recyclability. In addition, natural fiber composites have a minimal impact on the environment in regards to global warming, health, and pollution. Polylactic acid (PLA) is one of the best natural resource polymers available among biodegradable polymers. Natural fiber–reinforced PLA polymer composites have been extensively researched by polymer researchers to compete with conventional polymers. The type of fiber used plays a massive part in fiber and matrix bonds and, thereby, influences the composite's mechanical properties and thermal properties. Among the various natural fibers, low density, high strength bamboo fibers (BF) have attracted attention. PLA and bamboo fiber composites play a vital character in an extensive range of structural and non-structural applications. This review briefly discussed on currently developed PLA-based natural bamboo fiber–reinforced polymer composites concentrating on the property affiliation of fibers. PLA polymer–reinforced natural bamboo fiber used to establish composite materials, various composite fabrication methods, various pretreatment methods on fibers, their effect on mechanical properties, as well as thermal properties and applications on different fields of such composites are discussed in this study. This review also presents a summary of the issues in the fabrication of natural fiber composites. [ABSTRACT FROM AUTHOR]

Recent years have observed a significant increase in the use of degradable materials in medicine due to their minimal impact on the patient and broad range of applicability. The biodegradable polymer Polydioxanone (PDO) provides a good example of the use of such one polymer that can represent the aforementioned medical materials in the field of medicine, due to its high level of biocompatibility and interesting mechanical properties. PDO is used to produce absorbable medical devices such as sutures and stents, and is also suitable for the fabrication of certain orthopedic implants. Polydioxanone can be processed using the injection molding method due to its thermoplastic nature; this method allows for the precise and easily-controllable production of medical materials without the need for toxic additives. A number of small commercial polymer implants have recently been introduced onto the market based on this processing method. It is important to note that, to date, no relevant information on the molding of PDO is available either for the scientific or the general public, and no study has been published that describes the potential of the injection molding of PDO. Hence, we present our research on the basic technological and material parameters that allow for the processing of PDO using the laboratory microinjection molding method. In addition to determining the basic parameters of the process, the research also focused on the study of the structural and mechanical properties of samples based on the thermal conditions during processing. A technological frame work was successfully determined for the processing of PDO via the microinjection molding approach that allows for the production of samples with the required homogeneity, shape stability and surface quality in a laboratory scale. The research revealed that PDO is a polymer with a major share of crystalline phases, and that it is sensitive to the annealing temperature profile in the mold, which has the potential to impact the final crystalline structure, the fracture morphology and the mechanical properties. [ABSTRACT FROM AUTHOR]

This study gives an overview of the most relevant processing and performance properties of a wide selection of biobased and biodegradable plastic materials that are currently commercially available. It provides the most extensive and up-to-date scientific overview of critical properties of biobased and biodegradable plastics. Materials that are tested include fully biobased polymers (polylactic acid, polyethylene, polyamide 10,10 and a range of polyhydroxy alkanoates), partially biobased polymers (polybutylene succinate, polybutylene succinate adipate, cellulose acetate, cellulose acetate propionate, polyethylene terephthalate, polytrimethylene terephthalate, an isosorbide based polycarbonate, a thermoplastic urethane and a starch based blend) and a number of fossil-based materials (polycaprolactone, polybutylene adipate terephthalate, polyglycolic acid and polypropylene). The mechanical (tensile, flexural, impact resistance and hardness), thermal (glass transition temperature, melting temperature, melt-flow index and haul-off force) and barrier (oxygen transmission rate, water vapour transmission rate) properties of all these materials were measured and are presented in a comprehensive overview. This overview shows that the majority of functionalities that are currently being offered by fossil based polymers can be met by biobased alternatives and by biodegradable materials if this is considered to be favourable at end-of-life.

In this work, the development of nanocomposite systems based on reduced graphite oxide (rGO) was combined with the development of crosslinked materials characterized by dynamic covalent bonds, i.e., a covalent associative network, starting from ad-hoc synthesized hydroxyl terminated polycaprolactone (PCL-OH). The crosslinking reaction was carried out using methylenediphenyl diisocyanate (MDI) to create systems capable of bond exchanges via transesterification and transcarbamoylation reactions, in the presence of stannous octoate as a catalyst. The above materials were prepared at two different temperatures (120 and 200 °C) and two PCL-OH:MDI ratios. FT-IR measurements proved the formation of urethane bonds in all the prepared samples. Crosslinking was demonstrated by contacting the samples with a solvent capable of dissolving the star-shaped PCL. These tests showed a significant increase in the crosslinked fraction with increasing the temperature and the PCL-OH:MDI ratio. In order to evidence the effect of crosslinking on rGO dispersion and the final properties of the material, a nanocomposite sample was also prepared using a linear commercial PCL, with the nanofiller mixed under the same conditions used to develop the crosslinked systems. The dispersion of rGO, which was investigated using FE-SEM measurements, was similar in the different systems prepared, indicating that the crosslinking process had a minor effect on the dispersibility of the nanofiller. As far as the thermal properties are concerned, the DSC measurements of the prepared samples showed that the crosslinking leads to a decrease in the crystallinity of the polymer, a phenomenon which was particularly evident in the sample prepared at 200 °C with a PCL-OH: MDI ratio of 1:1.33 and was related to the decrease in the polymer chain mobility. Moreover, rGO was found to act as a nucleating agent and increase the crystallization temperature of the nanocomposite sample based on linear commercial PCL, while the contribution of rGO in the crosslinked nanocomposite samples was minor. Rheological measurements confirmed the crosslinking of the PCL-OH system which generates a solid-like behavior depending on the PCL-OH:MDI ratio used. The presence of rGO during crosslinking generated a further huge increase in the viscosity of the melt with a remarkable solid-like behavior, confirming a strong interaction between rGO and crosslinked PCL. Finally, the prepared nanocomposites exhibited self-healing and recyclability properties, thus meeting the requirements for sustainable materials. [ABSTRACT FROM AUTHOR]

In 2021, global petroleum-based plastic production reached over 400 million metric tons (Mt), and the accumulation of these non-biodegradable plastics in the environment is a worldwide concern. Polyhydroxybutyrate (PHB) offers many advantages over traditional petroleum-based plastics, being biobased, completely biodegradable, and non-toxic. However, its production and use are still challenging due to its low deformation capacity and narrow processing window. In this work, two linear-chain polyester oligomers were used as plasticizers to improve the processability and properties of PHB. Thermal analyses, XRD, and polarized optical microscopy were performed to evaluate the plasticizing effect on the PHB and the reflection on the mechanical behavior. Both oligomers acted as PHB plasticizers, with a reduction in Tg and Tm as a function of the plasticizer concentration, which can make it easier to handle the material in thermal processing and reduce the probability of thermal degradation. Plasticizer 2 proved to be the most promising between the two with an optimized condition of 20%, in which there was a decrease in elastic modulus of up to 72% and an increase in the maximum elongation of 467%. [ABSTRACT FROM AUTHOR]

Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) with various 3-hydroxyvalerate (3HV) contents biosynthesized by mixed microbial consortia (MMC) fed fermented dairy manure at the large-scale level was assessed over a 3-month period. The thermal, mechanical, and rheological behavior and the chemical structure of the extracted PHBV biopolymers were studied. The recovery of crude PHBV extracted in a large Soxhlet extractor with CHCl3 for 24 h ranged between 20.6% to 31.8% and purified to yield between 8.9% to 26.9% all based on original biomass. 13C-NMR spectroscopy revealed that the extracted PHBVs have a random distribution of 3HV and 3-hydroxybutyrate (3HB) units and with 3HV content between 16% and 24%. The glass transition temperature (Tg) of the extracted PHBVs varied between −0.7 and −7.4 °C. Some of the extracted PHBVs showed two melting temperatures (Tm) which the lower Tm1 ranged between 126.1 °C and 159.7 °C and the higher Tm2 varied between 152.1 °C and 170.1 °C. The weight average molar mass of extracted PHBVs was wide ranging from 6.49 × 105 g·mol−1 to 28.0 × 105 g·mol−1. The flexural and tensile properties were also determined. The extracted polymers showed a reverse relationship between the 3HV content and Young's modulus, tensile strength, flexural modulus, and flexural strength properties. [ABSTRACT FROM AUTHOR]

In this work, new furan-based poly(ester amide)s of various compositions were synthesised by the melt polycondensation method. The chemical structure and composition were determined by nuclear magnetic resonance spectroscopy (1H NMR) and Fourier transform infrared (FTIR) analyses. The optical properties were studied by UV-Vis spectroscopy. The thermal properties were investigated by means of differential scanning calorimetry (DSC). The thermo-oxidative stability of PEAs was also tested. Additionally, the free volume by positron annihilation lifetime spectroscopy (PALS) technique and mechanical properties were examined. It was found that the incorporation of poly(propylene furanamide) (PPAF) units significantly affects the thermal and mechanical properties of co-polymers based on poly(hexylene 2,5-furandicarboxylate) (PHF). Depending on the composition, both semi-crystalline and amorphous co-polymers were obtained. Moreover, the values of the free volume radius (R) and the free volume fractions (fv) were strongly affected by the mole fraction of PPAF units. [ABSTRACT FROM AUTHOR]

Poly(3−hydroxybutyrate−co−3−hydroxyhexanoate) (PHBH) films were prepared using a cast film technique. Dioxane was chosen over other polymer solvents as it resulted in homogenous films with better morphology. Several plasticizers with different molecular weights and concentrations were added to the biopolymer solution prior to casting. Thermal, crystalline, and permeability properties were analyzed by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), X−ray diffraction (XRD), and both water vapor and oxygen transmission rate analysis. In general, the addition of plasticizers decreased the glass transition temperature (Tg), cold crystallization temperatures (Tcc), melting temperatures, as well as crystallinity degrees and increased the crystallite sizes and water vapor and oxygen transmission rates. The use of isosorbide and low-molecular-weight poly(ethylene glycol) (PEG) lowered the Tg around 30 °C at the highest used concentration, also being the most effective in increasing the crystallite size. When considering isosorbide and low-molecular-weight poly(ethylene glycol) (PEG) as very good plasticizers for PHBH, the question of which plasticizer to use strongly relies on the desired PHBH application. [ABSTRACT FROM AUTHOR]

Reinforcement with natural fibre has become a common place in a range of industries in the modern day. A polymer matrix can, however, boost the strength of the reinforcing element. When it comes to natural fibres and polymers, they simply do not mix because of their different hydrophobic and hydrophilic properties. However, because the polymer matrix is designed to be hydrophobic, the natural fibres are hydrophilic. This issue can now be rectified with alkalization and a silane binding agent. This technique of modifying natural fibres may result in both rise in surface roughness and a reduction in water attraction and moisture content. In this research, the effects of alkaline and silane treatment were demonstrated using mechanical testing and Fourier transform infrared spectroscopy (FTIR). DSC and TGA tests were used to assess the materials' chemical compositions and thermal properties. In comparison to other composites, those with a 2 percent silane treatment showed improved strength performance. Hemp fibre composites are expected to achieve great performance in industrial applications by enduring chemical treatment. [ABSTRACT FROM AUTHOR]

Suitable packaging material in combination with high-pressure processing (HPP) can retain nutritional and organoleptic qualities besides extending the product's shelf life of food products. However, the selection of appropriate packaging materials suitable for HPP is tremendously important because harsh environments like high pressure and high temperature during the processing can result in deviation in the visual and functional properties of the packaging materials. Traditionally, fossil-based plastic packaging is preferred for the HPP of food products, but these materials are of serious concern to the environment. Therefore, bio-based packaging systems are proposed to be a promising alternative to fossil-based plastic packaging. Some studies have scrutinized the impact of HPP on the functional properties of biopolymer-based packaging materials. This review summarizes the HPP application on biopolymer-based film-forming solutions and pre-formed biopolymer-based films. The impact of HPP on the key packaging properties such as structural, mechanical, thermal, and barrier properties in addition to the migration of additives from the packaging material into food products were systemically analyzed. HPP can be applied either to the film-forming solution or preformed packages. Structural, mechanical, hydrophobic, barrier, and thermal characteristics of the films are enhanced when the film-forming solution is exposed to HPP overcoming the shortcomings of the native biopolymers-based film. Also, biopolymer-based packaging mostly PLA based when exposed to HPP at low temperature showed no significant deviation in packaging properties indicating the suitability of their applications. HPP may induce the migration of packaging additives and thus should be thoroughly studied. Overall, HPP can be one way to enhance the properties of biopolymer-based films and can also be used for packaging food materials intended for HPP. [ABSTRACT FROM AUTHOR]

Depletion of fossil fuels and the detrimental environmental impacts of synthetic plastics have prompted a global interest in bio-based polymers. Lignin is an abundant, unused, and low-value byproduct of pulping and biochemical operations that has the potential to decrease the need for plastics derived from petroleum. Melt blending is one of the easiest strategies for expanding the commercial applications of lignin. Concerns remain, however, regarding the negative effects of lignin on the final composite material's performance, and the increase in manufacturing costs. This study investigates the effects of blending lignin extracted from tobacco using a novel one-step processing technique on injection molding parameters, and the mechanical, physical, and thermal properties of high-density polyethylene (HDPE). By extruding HDPE pellets and lignin powder, varying blend concentrations (0, 5, 10, 15, and 30% wt.) were produced. Scanning electron microscopy (SEM) and optical microscopy were used to investigate the compatibility of the blend morphology. Results indicated that interfacial interactions were achieved as particles of tobacco lignin were well dispersed and uniformly distributed throughout HDPE. Intermolecular interactions between HDPE and lignin were also discovered through Fourier-transform infrared (FTIR) spectral analyses. The tensile test results showed that increase in lignin content up to 15% wt. had little effect on tensile strength, but at 30% wt., a 19% reduction was observed. With the addition of 5, 10, 15, and 30% wt. of lignin, the tensile modulus increased by 4%, 29%, 25%, and 8%, respectively. TGA results demonstrated that at 15% and 30% wt., tobacco lignin acted as a thermal stabilizer. The processability study revealed that tobacco lignin could be processed easily using injection molding without requiring significant changes to the process parameters. Overall, tobacco lignin showed great promise as a biodegradable HDPE filler. [ABSTRACT FROM AUTHOR]

A series of poly(ester amide)s based on dimethyl furan 2,5-dicarboxylate (DMFDC), 1,3-propanediol (PDO), 1,6-hexylene glycol (HDO), and 1,3-diaminopropane (DAP) were synthesized via two-step melt polycondensation. The phase transition temperatures and structure of the polymers were studied by differential scanning calorimetry (DSC). The positron annihilation lifetime spectroscopy (PALS) measurement was carried out to investigate the free volume. In addition, the mechanical properties of two series of poly(ester amide)s were analyzed. The increase in the number of methylene groups in the polymer backbone resulted in a decrease in the values of the transition temperatures. Depending on the number of methylene groups and the content of the poly(propylene furanamide) (PPAF), both semi-crystalline and amorphous copolymers were obtained. The free volume value increased with a greater number of methylene groups in the polymer backbone. Moreover, with a lower number of methylene groups, the value of the Young modulus and stress at break increased. [ABSTRACT FROM AUTHOR]

Improving the technological functionality of climate-resilient crops (CRCs) to promote their use in staple foods, such as bread, is relevant to addressing food and nutrition security in Africa. Dry heating of cowpea flour (CPF) was studied as a simple technology to modulate CPF physicochemical properties in relation to bread applications. For this purpose, the melting behavior of cowpea starch and proteins in CPF was first studied and modeled using Flory–Huggins theory for polymer melting. Next, dry-heating conditions were investigated based on the predicted biopolymer melting transitions in CPF to be well below starch and protein melting. The pasting properties (i.e., peak viscosity, final viscosity, breakdown and setback) of CPF could be selectively modulated depending on temperature-time combinations without altering the thermal behavior (i.e., melting enthalpies) of CPF. Water-binding capacity and soluble solids decreased with the increased severity of the temperature-time combinations. Dry-heated CPF added to CRC-based bread significantly improved crumb texture. In particular, dry heating at 100 °C for 2 h provided bread with the highest crumb softness, cohesiveness and resilience. The positive effects on the crumb texture could be largely related to enhanced starch integrity, as indicated by a reduction in breakdown viscosity after treatment. Overall, dry heating of CPF under defined conditions is a promising technology for promoting the use of CPF as a techno-functional and protein-rich ingredient in bread-type products. [ABSTRACT FROM AUTHOR]

Blends of poly(lactic acid) (PLA)/poly(3‐hydroxybutyrate) (PHB) (70/30 wt%) were prepared, and the effects of multiple mechanical recycling up to 5 times on the rheology–morphology relationships, thermal, and mechanical properties were investigated. Rheological and morphological investigations indicated a degree of immiscibility of two combined polymers. Notably, recycling served to improve the interfacial interaction of the phases through limited transesterification reactions and increased homogeneous morphologies. While there was significant reduction in viscosity through multiple recycling, chain scission and degradation were not observed in Fourier transform infrared (FTIR) results. Additionally, higher crystallinity and lower Tg and cold crystallization temperatures were measured for the reprocessed samples, which are attributed to the formation of finer PHB droplets acting as nucleating agents promoting further crystallinity. In conclusion, the increased crystallinity counter influenced the measured viscosity decrease, and subsequently, multiple recycling was not observed to significantly affect the tensile properties. Furthermore, impact results are also indicative of the crucial role of crystallinity and blend morphology on maintaining the toughness of the recycled samples. [ABSTRACT FROM AUTHOR]

Fungal biomass (FB), a by-product of the fermentation processes produced in large volumes, is a promising biomaterial that can be incorporated into poly(lactic acid) (PLA) to develop enhanced biocomposites that fully comply with the biobased circular economy concept. The PLA/FB composites, with the addition of triethyl citrate (TEC) as a biobased plasticizer, were fabricated by a microcompounder at 150 °C followed by injection molding. The effects of FB (10 and 20 wt %) and TEC (5, 10, and 15 wt %) contents on the mechanical, thermal and surface properties of the biocomposites were analyzed by several techniques. The PLA/FB/TEC composites showed a rough surface in their fracture section. A progressive decrease in tensile strength and Young's modulus was observed with increasing FB and TEC, while elongation at break and impact strength started to increase. The neat PLA and biocomposite containing 10% FB and 15% TEC exhibited the lowest (3.84%) and highest (224%) elongation at break, respectively. For all blends containing FB, the glass transition, crystallization and melting temperatures were shifted toward lower values compared to the neat PLA. The incorporation of FB to PLA thus offers the possibility to overcome one of the main drawbacks of PLA, which is brittleness. [ABSTRACT FROM AUTHOR]

This research aimed to investigate the effects of using wood leachate (WL) powder as a cost-effective filler added to novel poly (lactic acid) biocomposites and evaluate their mechanical, thermal, morphological, and antibacterial properties. Fourier transform infrared spectroscopy (FTIR), tensile test, Charpy impact test, Shore hardness, scanning electron microscope (SEM), differential scanning calorimetry (DSC), contact angle, and bacterial growth inhibition tests were employed to characterize the developed biocomposites. The SEM results indicated a proper filler dispersion in the polymer matrix. WL powder improved the hydrophobic nature in the adjusted sample's contact angle experiment. Markedly, the results showed that the addition of WL filler improved the mechanical properties of the fabricated biocomposites. The thermal analysis determined the development in crystallization behavior and a decline in glass transition temperature (Tg) from 60.1 to 49.3 °C in 7% PLA-WL biocomposites. The PLA-WL biocomposites exhibited an antibacterial activity according to the inhibition zone for Escherichia coli bacteria. The developed novel PLA-WL composites can be effectively utilized in various value-added industrial applications as a sustainable and functional biopolymer material. [ABSTRACT FROM AUTHOR]

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In ongoing decades, material researchers and scientists are giving more consideration towards the improvement of biobased polymer composites as various employments of items arranged by natural fibres and petrochemical polymers prompt natural awkwardness. The goal of this review paper is to provide an intensive review and applications of the foremost appropriate commonly used biodegradable polymer composites. It is imperative to build up the completely/incompletely biodegradable polymer composites without bargaining the mechanical, physical, and thermal properties which are required for the end-use applications. This reality roused to create biocomposite with better execution alongside the least natural effect. The utilization of natural fibre-reinforced polymer composites is concerned with the mechanical properties that are highly dependent on the morphology, hydrophilic tendency, aspect ratio, and dimensional stability of the natural fibre. With this in-depth consideration of eco-friendly biocomposites, structural application materials in the infrastructure, automotive industry, and consumer applications of the following decade are attainable within the near future. [ABSTRACT FROM AUTHOR]

The development of biodegradable materials as food packaging material is important not only due to the reduction in environmental pollution but also because of an improvement in the functionality. Rice husk-reinforced biopolymers have offered a possible solution to waste-disposal problems associated with traditional petroleum-derived plastics. Rice husk-reinforced low density polyethylene (LDPE)-based biocomposites have been of great interest for their use as food packaging material. In this work, the LDPE/RH biocomposites with different rice husk (RH) content (10, 20, 30, 40 and 50 wt.%) were prepared by the melt mixing process in a laboratory Brabender mixer. The effect of RH content on the physical, thermal and mechanical properties of LDPE was investigated. More importantly, this work aimed to research the biodegradation of the LDPE/RH biocomposites as well as their effect on ‘Granny Smith’ apples’ respiration. The results showed that the incorporation of RH into the LDPE decreased the thermal stability of LDPE, increased water vapour permeability and water absorption, and increased the degree of crystallinity. The incorporation of RH increased the biodegradability of LDPE as well as the postharvest quality of ‘Granny Smith’ apples. The addition of RH in LDPE film significantly decreased fruit respiration and increased firmness as compared to LDPE film. The composting results showed that after the LDPE/RH biocomposite films were biodegraded for 21 days, the biocomposite films with the highest content of rice husks were the most degraded. [ABSTRACT FROM AUTHOR]

There is more demand for natural fiber-reinforced composites in the energy sector, and their impact on the environment is almost zero. Natural fiber has plenty of advantages, such as easy recycling and degrading property, low density, and low price. Natural fiber's thermal properties and flexural properties are less than conventional fiber. This work deals with the changes in the thermal properties and mechanical properties of S-glass reinforced with a sodium hydroxide-treated pineapple leaf (PALF) and banana stem fibers. Banana stem and pineapple leaf fibers (PALF) were used at various volume fractions, i.e., 30%, 40%, and 50%, and various fiber lengths of 20 cm, 30 cm, and 40 cm with S-glass, and their effects on the thermal and mechanical properties were studied, and their optimum values were found. It was evidenced that increasing the fiber volume and fiber length enhanced the flexural and thermal properties up to 40% of the fiber volume, and started to decrease at 50% of the fiber volume. The fiber length provides an affirmative effect on the flexural properties and a pessimistic effect on the thermal properties. The PALF S-glass combination of 40% fiber load and 40 cm fiber length provides maximum flexural strength, flexural modulus, storage modulus, and lowest loss modulus based on hybrid Taguchi grey relational optimization techniques. PALF S-glass hybrid composite has been found to have 7.80%, 3.44%, 1.17% higher flexural strength, flexural modulus, and loss modulus, respectively, and 15.74% lower storage modulus compared to banana S-glass hybrid composite. [ABSTRACT FROM AUTHOR]

In 2021, global petroleum-based plastic production reached over 400 million metric tons (Mt), and the accumulation of these non-biodegradable plastics in the environment is a worldwide concern. Polyhydroxybutyrate (PHB) offers many advantages over traditional petroleum-based plastics, being biobased, completely biodegradable, and non-toxic. However, its production and use are still challenging due to its low deformation capacity and narrow processing window. In this work, two linear-chain polyester oligomers were used as plasticizers to improve the processability and properties of PHB. Thermal analyses, XRD, and polarized optical microscopy were performed to evaluate the plasticizing effect on the PHB and the reflection on the mechanical behavior. Both oligomers acted as PHB plasticizers, with a reduction in Tg and Tm as a function of the plasticizer concentration, which can make it easier to handle the material in thermal processing and reduce the probability of thermal degradation. Plasticizer 2 proved to be the most promising between the two with an optimized condition of 20%, in which there was a decrease in elastic modulus of up to 72% and an increase in the maximum elongation of 467%.

Poly(3−hydroxybutyrate−co−3−hydroxyhexanoate) (PHBH) films were prepared using a cast film technique. Dioxane was chosen over other polymer solvents as it resulted in homogenous films with better morphology. Several plasticizers with different molecular weights and concentrations were added to the biopolymer solution prior to casting. Thermal, crystalline, and permeability properties were analyzed by thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), X−ray diffraction (XRD), and both water vapor and oxygen transmission rate analysis. In general, the addition of plasticizers decreased the glass transition temperature (Tg), cold crystallization temperatures (Tcc), melting temperatures, as well as crystallinity degrees and increased the crystallite sizes and water vapor and oxygen transmission rates. The use of isosorbide and low-molecular-weight poly(ethylene glycol) (PEG) lowered the Tg around 30 °C at the highest used concentration, also being the most effective in increasing the crystallite size. When considering isosorbide and low-molecular-weight poly(ethylene glycol) (PEG) as very good plasticizers for PHBH, the question of which plasticizer to use strongly relies on the desired PHBH application.

A series of poly(ester amide)s based on dimethyl furan 2,5-dicarboxylate (DMFDC), 1,3-propanediol (PDO), 1,6-hexylene glycol (HDO), and 1,3-diaminopropane (DAP) were synthesized via two-step melt polycondensation. The phase transition temperatures and structure of the polymers were studied by differential scanning calorimetry (DSC). The positron annihilation lifetime spectroscopy (PALS) measurement was carried out to investigate the free volume. In addition, the mechanical properties of two series of poly(ester amide)s were analyzed. The increase in the number of methylene groups in the polymer backbone resulted in a decrease in the values of the transition temperatures. Depending on the number of methylene groups and the content of the poly(propylene furanamide) (PPAF), both semi-crystalline and amorphous copolymers were obtained. The free volume value increased with a greater number of methylene groups in the polymer backbone. Moreover, with a lower number of methylene groups, the value of the Young modulus and stress at break increased.

[Display omitted] • Radical polymerization mechanisms details of fumarate monomers are reviewed. • Structural characteristics, thermal properties and thermoresponsive behavior of fumaric homo and copolymers are presented. • Blend, composites, and copolymers with fumaric structures, employed as biomaterials are presented. • Applications of fumaric copolymers as flow improver and asphalt modifiers are descripted in this review. Fumaric polymers are macromolecules obtained from 1,2-disubstituted monomers, which provide special structural characteristics and therefore attractive physicochemical properties for their applications. Thus, in the present review, different radical polymerization mechanisms (conventional or living) are detailed and their characteristic kinetic parameters are shown. For example, the use of the initiator 2,2′-azobis(isobutyrate) (MAIB) allows to obtain polymers of higher molecular weight since it generates more stable primary radicals than those achieved with other azo initiators. The emergence of different controlled radical polymerization methodologies has resulted in the generation of new fumaric homo and copolymers with different properties. The structural characteristics of these materials analyzed by spectroscopic techniques and their relationship with properties in solutions, glass transition temperature, thermal stability and mechanical behavior are detailed in the present work. Finally, several biomedical and energy applications are described in which copolymers from fumaric and acrylic monomers were employed, combined or not with natural polymers to be used as scaffolds in the regeneration of bone and cartilage tissue, drug delivery systems, as flow or asphalt modifiers. From the complete reading of this review, it will be possible to achieve a global vision starting from the synthesis to the application of fumaric polymers in which the need of scaling this type of productions to reach specific industrial applications is visualized. [ABSTRACT FROM AUTHOR]

This study gives an overview of the most relevant processing and performance properties of a wide selection of biobased and biodegradable plastic materials that are currently commercially available. It provides the most extensive and up-to-date scientific overview of critical properties of biobased and biodegradable plastics. Materials that are tested include fully biobased polymers (polylactic acid, polyethylene, polyamide 10,10 and a range of polyhydroxy alkanoates), partially biobased polymers (polybutylene succinate, polybutylene succinate adipate, cellulose acetate, cellulose acetate propionate, polyethylene terephthalate, polytrimethylene terephthalate, an isosorbide based polycarbonate, a thermoplastic urethane and a starch based blend) and a number of fossil-based materials (polycaprolactone, polybutylene adipate terephthalate, polyglycolic acid and polypropylene). The mechanical (tensile, flexural, impact resistance and hardness), thermal (glass transition temperature, melting temperature, melt-flow index and haul-off force) and barrier (oxygen transmission rate, water vapour transmission rate) properties of all these materials were measured and are presented in a comprehensive overview. This overview shows that the majority of functionalities that are currently being offered by fossil based polymers can be met by biobased alternatives and by biodegradable materials if this is considered to be favourable at end-of-life. • The most extensive and up-to-date scientific overview of critical properties of biobased and/or biodegradable plastics. • Mechanical properties characterized; tensile, flexural, impact resistance and hardness. • Thermal properties characterized; glass transition temperature, melting temperature, melt-flow index and haul-off force. • Barrier properties characterized; oxygen transmission rate, water vapour transmission rate. [ABSTRACT FROM AUTHOR]

Nanocellulose fibers are widely acknowledged as a more sustainable alternative to polyimide and polyethylene terephthalate-based plastic films derived from petrochemicals. Cellulose is also utilised in packaging, tissue engineering, electronic, optical, and sensor applications, pharmaceutical applications, cosmetic applications, insulation, water filtration, and hygiene applications, as well as vascular grafts. In the present study to improve the tensile and thermal properties of cellulose nanofibers, polyethylene glycol (PEG 600) with varying concentrations was produced by solvent casting and chemically crosslinked with glutaraldehyde (GA). The effects of various PEG 600 concentrations on nanofibers and the morphology of the resulting nanofibers were investigated. The effects of GA on PEG-nanocellulose morphology, average diameter, tensile strength, elongation, and thermal characteristics were investigated. Strong (GA)-based acetal linkages are used to substitute secondary hydrogen bonds in nanocellulose films. The 1% PEG 600 plasticized nanocellulose scaffolds cross-linked with GA showed a higher tensile modulus (93 MPa) than its GA untreated nanocellulose scaffolds (69 MPa). The Young's modulus of the scaffold is increased up to 83.62 MPa. The crystallinity index values of GA-treated scaffolds were increased, and the mechanical characteristics were greatly improved, according to Fourier transform infrared (FTIR) and XRD analysis on the films. The thermogravimetric analysis (TG/DTG/DSC) of the GA treated plasticized nanocellulose scaffold showed maximum decomposition temperature (T max) at 360.01 °C. [Display omitted] • Nanocellulose fibers are extracted from the plant roots of Ixora coccinea L. • Fabricated with solvent casting process, plasticized with PEG 600, and glutaraldehyde crosslinked. • Tensile modulus of 1% PEG 600 plasticized nanocellulose scaffolds cross-linked with GA was greater (93 MPa). • The thermogravimetric analysis of the scaffold showed T max at 360.01 °C. [ABSTRACT FROM AUTHOR]

In this work, a series of antibacterial cationic copolymers derived from bio-sourced itaconic acid was studied as potential biobased active components in biodegradable formulations based on poly(butylene adipate- co -terephthalate) (PBAT) for packaging applications. These copolymers were first characterized by testing their antimicrobial activity against resistant bacterial strains, their biodegradability in compost conditions, and their thermal properties by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The antibacterial properties showed potent activity against Methicillin-resistant Staphylococcus aureus (MRSA), with MIC values as low as 78 μg mL−1. Related to their biodegradability, the cationic polymers biodegraded fast under compost conditions and even a priming effect was observed in the compost. Thermal properties, characterized by DSC and TGA, showed that the copolymers thermally degraded at temperature relatively low; nevertheless, they are able to be processed at temperatures up to ∼150 °C. Subsequently, these antibacterial polymers were successfully blended as minor active component (10 wt%) with PBAT by melt-extrusion and press-compression molding. The resulting biopolymeric films exhibit potent antibacterial activity, which confirm that the cationic polymers incorporated as active component are able to perverse this activity after the processing and impart antibacterial properties to PBAT bioplastic. Therefore, these antibacterial biobased polymers derived from itaconic acid seem to be good candidates for applications related to active food packaging or even for biomedical devices. Novel biodegradable polymers derived from bio-sourced itaconic acid were incorporated as potential antimicrobial component in a biopolymeric blend formulation based on fully biodegradable poly(butylene adipate- co -terephthalate) (PBAT). [Display omitted] • Antibacterial biopolymers derived from itaconic acid display high activity against MRSA. • Antibacterial biopolymers are able to biodegrade fast under compost conditions. • Antibacterial biopolymers were incorporated in PBAT-based blend films. [ABSTRACT FROM AUTHOR]

The electrospinnability of FucoPol, a bacterial exopolysaccharide, is presented for the first time, evaluated alone and in combination with other polymers, such as polyethylene oxide (PEO) and pullulan. The obtained fibers were characterized in terms of their morphological, structural and thermal properties. Pure FucoPol fibers could not be obtained due to FucoPol's low water solubility and a lack of molecular entanglements. Nanofibers were obtained via blending with PEO and pullulan. FucoPol:PEO (1:3 w/w) showed fibers with well-defined cylindrical structure, since the higher molecular weight of PEO helps the continuity of the erupted jet towards the collector, forming stable fibers. WAXS, DSC and TGA showed that FucoPol is an amorphous biopolymer, stable until 220 °C, whereas FucoPol-PEO fibers were stable until 140 °C, and FucoPol:pullulan fibers were stable until 130 °C. Interestingly, blended components influenced one another in intermolecular order, since new peaks associated to intermolecular hierarchical assemblies were seen by WAXS. These results make FucoPol-based systems viable candidates for production of nanofibers for packaging, agriculture, biomedicine, pharmacy and cosmetic applications. [ABSTRACT FROM AUTHOR]

[Display omitted] • Successful preparation protocol of the anhydrous nanocomposite proton conductor. • The U.S. Department of Energy durability standards for fuel cell membranes met. • Proton transport determined by the molecular reorientation of the triazole ring. We designed and synthesized new proton-conducting materials (CNC-Tri) based on natural polymer composed of nanocrystalline cellulose (CNC) doped with different concentrations of 1 H -1,2,3 triazole (Tri). The CNC functionalization with Tri does not affect cellulose structure. The material has the form of semitransparent polymer film. The presence of Tri in the CNC matrix was confirmed by the infrared spectra. The activation energies for the desorption of water, triazole evaporation, and the degradation of the CNC matrix, were evaluated. The proton conduction takes place under anhydrous conditions up to 180 °C and the highest value of conductivity is equal to 4.0 × 10-4 S/m at 160 °C. The behavior of conductivity is consistent with the Grotthuss mechanism and proton transport is conditioned by the triazole ring reorientation revealed by the solid-state 1H- 13C CPMAS NMR. CNC-Tri was found to show better thermal properties when compared to the previously tested CNC doped with imidazole (Im), but with lower conductivity. Possible reasons for these differences are discussed in this article. [ABSTRACT FROM AUTHOR]

In this study, the effects of various quantities of sorbitol and glycerol plasticizers (0%, 30%, 45%, and 60%) on cornstarch-based film were examined to develop a novel polymer for usage with biodegradable materials. The film was prepared using the casting process. According to the test findings, the application of the plasticizer concentrations affected the thickness, moisture content, and water absorption of the film. When plasticizer concentrations were increased to 60%, the tensile stress and Young's modulus of plasticized films dropped regardless of plasticizer type. However, the thin film with addition of 30% sorbitol plasticizer demonstrated a steady value of Young's modulus (60.17 MPa) with an increase in tensile strength (13.61 MPa) of 46%, while the lowest combination of tensile strength and Young's modulus is the film that was plasticized with 60% glycerol, with 2.33 MPa and 16.23 MPa, respectively. In summary, the properties and performance of cornstarch-based film were greatly influenced by plasticizer types and concentrations. The finest set of features in this research appeared in the film plasticized with 30% sorbitol, which achieved the best mechanical properties for food packaging applications. [ABSTRACT FROM AUTHOR]

Industry-sponsored research has intensified to find suitable substitutes for synthetic polymers. For this purpose, biopolymers are promising materials that are extracted from renewable resources. However, there are areas of concern (biopolymers are mostly brittle in the dry state) that require further research before they are used in advanced applications. To overcome this, plasticizers are often added to biopolymers to enhance their physicochemical properties. In this study, chitosan (CH)-glycerol (GL)-based polymeric films were prepared by a simple drop-casting technique, and the influence of a plasticizer (GL) on the properties of chitosan films was analyzed. Additionally, the as-prepared samples were irradiated with γ-rays (60Co γ rays with a dose of 102 kGy) to study the effect of γ-irradiation on the properties of polymeric composites. To achieve this, different samples were prepared by varying the amount of GL. FT-IR analysis revealed the interruption of hydrogen bonding in chitosan by the incorporation of GL. This led to the chain-spreading of CH, which ultimately increased the flexibility of the composite films (CH-GL). The DSC of the CH film showed two peaks: one endothermic peak below 100 °C (due to water vapor) and a second exothermic peak that appeared between 130 and 360 °C (degradation of the amino group). Plasticization of CH films with GL was confirmed by DSC, where the exothermic degradation was converted into an endothermic peak. Depending upon the amount of GL, γ-irradiation considerably affected the chemical structure of CH by breaking the carbohydrate and pyranose rings; this led to a decrease in the crystallinity of the composite films. The changes studied in the DSC and TGA analysis complemented each other. γ-irradiation also affected the morphology of the films, which changed from smooth and homogeneous to roasted structures, with random swelling on the surface of the films. This swelling reflected the degradation of the surfaces into thin layers. Considering the changes that occurred in the films post-γ-irradiation, it can be inferred that the irradiation dose of 102 kGy is sufficient to degrade as-prepared biopolymer composites. [ABSTRACT FROM AUTHOR]

An eco-friendly strategy for the modification of polylactic acid (PLA) surface properties, using a solvent-free process, is reported. Reactive extrusion (REX) allowed the formation of new covalent bonds between functional molecules and the PLA polymeric matrix, enhancing its mechanical properties and modifying surface hydrophobicity. To this end, the PLA backbone was modified using two alkoxysilanes, phenyltriethoxysilane and N-octyltriethoxysilane. The reactive extrusion process was carried out under mild conditions, using melting temperatures between 150 and 180 °C, 300 rpm as screw speed, and a feeding rate of 3 kg·h−1. To complete the study, flat tapes of neat and functionalized PLA were obtained through monofilament melt extrusion to quantify the enhancement of mechanical properties and hydrophobicity. The results verified that PLA modified with 3 wt% of N-octyltriethoxysilane improves mechanical and thermal properties, reaching Young's modulus values of 4.8 GPa, and PLA hydrophobic behavior, with values of water contact angle shifting from 68.6° to 82.2°. [ABSTRACT FROM AUTHOR]

Biocomposites comprising a combination of natural fibres and bio-based polymers are good alternatives to those produced from synthetic components in terms of sustainability and environmental issues. However, it is well known that water or aqueous chemical solutions affect natural polymers/fibres more than the respective synthetic components. In this study the effects of water, salt water, acidic and alkali solutions ageing on water uptake, mechanical properties and flammability of natural fibre-reinforced polypropylene (PP) and poly(lactic acid) (PLA) composites were compared. Jute, sisal and wool fibre- reinforced PP and PLA composites were prepared using a novel, patented nonwoven technology followed by the hot press method. The prepared composites were aged in water and chemical solutions for up to 3 week periods. Water absorption, flexural properties and the thermal and flammability performances of the composites were investigated before and after ageing each process. The effect of post-ageing drying on the retention of mechanical and flammability properties has also been studied. A linear relationship between irreversible flexural modulus reduction and water adsorption/desorption was observed. The aqueous chemical solutions caused further but minor effects in terms of moisture sorption and flexural modulus changes. PLA composites were affected more than the respective PP composites, because of their hydrolytic sensitivity. From thermal analytical results, these changes in PP composites could be attributed to ageing effects on fibres, whereas in PLA composite changes related to both those of fibres present and of the polymer. Ageing however, had no adverse effect on the flammability of the composites. [ABSTRACT FROM AUTHOR]