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Bacterial cellulose (BC) is recognized as a multifaceted, versatile biomaterial with abundant applications. Groups of microorganisms such as bacteria are accountable for BC synthesis through static or agitated fermentation processes in the presence of competent media. In comparison to static cultivation, agitated cultivation provides the maximum yield of the BC. A pure cellulose BC can positively interact with hydrophilic or hydrophobic biopolymers while being used in the biomedical domain. From the last two decades, the reinforcement of biopolymer-based biocomposites and its applicability with BC have increased in the research field. The harmony of hydrophobic biopolymers can be reduced due to the high moisture content of BC in comparison to hydrophilic biopolymers. Mechanical properties are the important parameters not only in producing green composite but also in dealing with tissue engineering, medical implants, and biofilm. The wide requisition of BC in medical as well as industrial fields has warranted the scaling up of the production of BC with added economy. This review provides a detailed overview of the production and properties of BC and several parameters affecting the production of BC and its biocomposites, elucidating their antimicrobial and antibiofilm efficacy with an insight to highlight their therapeutic potential.

Today, plant fibers are considered as an important new renewable resource that can compete with some synthetic fibers, such as glass, in fiber-reinforced composites. In previous works, it was noted that the pectin-enriched middle lamella (ML) is a weak point in the fiber bundles for plant fiber-reinforced composites. ML is strongly bonded to the primary walls of the cells to form a complex layer called the compound middle lamella (CML). In a composite, cracks preferentially propagate along and through this layer when a mechanical loading is applied. In this work, middle lamellae of several plant fibers of different origin (flax, hemp, jute, kenaf, nettle, and date palm leaf sheath), among the most used for composite reinforcement, are investigated by atomic force microscopy (AFM). The peak-force quantitative nanomechanical property mapping (PF-QNM) mode is used in order to estimate the indentation modulus of this layer. AFM PF-QNM confirmed its potential and suitability to mechanically characterize and compare the stiffness of small areas at the micro and nanoscale level, such as plant cell walls and middle lamellae. Our results suggest that the mean indentation modulus of ML is in the range from 6 GPa (date palm leaf sheath) to 16 GPa (hemp), depending on the plant considered. Moreover, local cell-wall layer architectures were finely evidenced and described.

Highlights The study presents the ideal distribution of graphene nanoplatelets (GNP) within the thermoplastic starch (TPS) matrix significantly elevated the thermal and electrical conductivities, as well as the electrochemical efficiency of the biocomposites. Additionally, the incorporation of GNP resulted in an increased thermal stability for the TPS, as indicated by the elevated temperatures required for maximum degradation. The biocomposites exhibited a self‐aligned layered structure, creating conductive pathways and enhancing electron conduction. An electrical conductivity increased as the concentration of GNP increased, with the highest conductivity observed on the top and bottom surface with the value of 4.23 × 10−7 S/m and 3.92 × 10−6 S/m when 12 wt% of GNP was added. The presence of hydroxyl groups in TPS facilitated the formation of hydrogen bonds with GNP, preventing GNP from stacking and forming a more uniform conductive network within the film. The addition of 15 wt% GNP also improved the capacitive performance of the TPS matrix, as evidenced by higher current responses and larger quasi‐rectangular areas in the cyclic voltammetry curves compared to neat TPS. The Nyquist plots which are illustrated impedance data showed that the TPS film with 12 wt% GNP exhibits the smallest semicircle, indicating the highest conductivity which is suggested that GNP improves charge transfer compared to pure TPS. Optimal dispersion of GNP enhanced the biocomposite's properties. The electrical conductivity increases with the GNP content until 12 wt%. TPS/GNP self‐aligned layered improved conduction and capacitive behavior. GNP improved thermal stability by restricting polymer chain movement. Electrochemical impedance shows improved properties of TPS/GNP. [ABSTRACT FROM AUTHOR]

The purpose of this study is to extract cellulose from corn silk (CS) fiber and use it as a reinforcing filler in unsaturated polyester resin (UPR) matrix. In this study, the cellulose is characterized using a Fourier Transform Infrared Spectrometer (FTIR), and the resulting UPR/cellulose biocomposite's mechanical properties (such as flexural and impact testing) are assessed. Scanning electron microscopy (SEM) provided strong support for mechanical rather than a chemical bond between fiber and UPR. Additionally, the sodium hydroxide treated CS in UPR biocomposite and comparing it with neat UPR. The agricultural byproduct rich in cellulose corn silk is a natural polymer known for its structural strength and UPR has garnered attention as a biopolymer with notable flexibility, making it an appealing choice for plastic product manufacturing. However, the drawback of UPR lies in its inherent deficiency in both stiffness and strength. According to the FTIR data, extracted cellulose (CS) had fewer ketone (C = O) and hydroxyl (-OH) groups than virgin cellulose. It was shown that throughout the extraction process, hemicellulose and lignin were more eliminated, producing a more pure form of cellulose. When filled in UPR, cellulose and treated CS both caused the impact strength of UPR biocomposites to drop. For both treated CS and cellulose, it was shown that the flexural modulus and flexural strength increased as the filler amount increased to a definite percentage (12%) after which it decreased. The result revealed the tensile strength and tensile modulus achieved by 0% of fiber with 48 N/mm2 and 51 N/mm2 and highest at 12% of fiber with 54.3 N/mm2 and 68.8 N/mm2 for CS + UPR. And 53.4 N/mm2 and 69.6 N/mm2 for cellulose + UPR composite,, respectively. In comparison, the flexural characteristics of UPR/cellulose were marginally inferior to those of UPR/treated CS. However, the impact resistance showed a significant improvement, particularly with a cellulose loading of 12%. Hence, cellulose presents a greater potential for composite manufacturing due to its ability to maintain the ductile properties of UPR compared to treated CS. Moreover, processed CS and cellulose both can be used as reinforcing agents in polymers to increase their strength and stiffness. [ABSTRACT FROM AUTHOR]

Synthetic polymers have made advances in terms of their flexibility and other properties but a major problem still exists when it comes to their poor biodegradability and lack of conservation. To overcome this problem, the biocomposites are widely used for wide range of applications. Crop residues (CRs) from agriculture can be utilized to make items like biodegradable components; however, they are hard to recycle or dispose of. The aim is to use corn cob ash (CCA), which is generated by calcination of corn cob (CC) in a pectin matrix to create a biocomposites. The Fourier transform infrared (FTIR), X‐ray diffraction (XRD), and energy‐dispersive X‐ray analysis (EDX) show the major compounds present in the CCA are silica, potassium, calcium, and many other inorganic compounds. In this research, a solution casting method is used to fabricate pectin/CC biocomposite films. By increasing the content of the CCA, the moisture content will decrease, contact angle and hardness properties are increased. However, increasing CCA content promotes the color change of pectin/CC biocomposite films and water absorption increases. The composite films are analyzed for biodegradation study. The FTIR, morphological, mechanical property, XRD, and thermogravimetric analysis (TGA) studies are used to evaluate the biocomposite films. [ABSTRACT FROM AUTHOR]

Biopolymers are biodegradable and renewable and can significantly reduce environmental impacts. For this reason, biocomposites based on a plasticized starch and cross-linker matrix and with a microfibrillated OCC cardboard cellulose reinforcement were developed. Biocomposites were prepared by suspension casting with varied amounts of microfibrillated cellulose: 0, 4, 8, and 12 wt%. Polyethylene glycol diglycidyl ether (PEGDE) was used as a cross-linking, water-soluble, and non-toxic agent. Microfibrillated cellulose (MFC) from OCC cardboard showed appropriate properties and potential for good performance as a reinforcement. In general, microfiber incorporation and matrix cross-linking increased crystallization, reduced water adsorption, and improved the physical and tensile properties of the plasticized starch. Biocomposites cross-linked with PEGDE and reinforced with 12 wt% MFC showed the best properties. The chemical and structural changes induced by the cross-linking of starch chains and MFC reinforcement were confirmed by FTIR, NMR, and XRD. Biodegradation higher than 80% was achieved for most biocomposites in 15 days of laboratory compost. [ABSTRACT FROM AUTHOR]

This study explores the synthesis and characterization of chitosan/gelatine films incorporating nickel ferrite (NiFe2O4) and cobalt ferrite (CoFe2O4) nanoparticles. The magnetic nanoparticles exhibit superparamagnetic behaviour, making them attractive for various applications, including biomedical uses. The X-ray diffraction analysis confirmed the successful synthesis of NiFe2O4 and CoFe2O4 nanoparticles, and the scanning electron micrographs illustrated well-dispersed ferrite nanoparticles within the biopolymer network, despite the formation of some aggregates attributed to magnetic interactions. Magnetization loops revealed lower saturation magnetization values for the composites, attributed to the chitosan/gelatine coating and the dielectric studies, indicating increased dielectric losses in the presence of ferrites, particularly pronounced in the case of NiFe2O4, suggesting interactions at the interface region between the polymer and ferrite particles. The AC conductivity shows almost linear frequency dependence, associated with proton polarization and conduction processes, more significant at higher temperatures for samples with ferrite particles. [ABSTRACT FROM AUTHOR]

The fiber-filled polymer composite is one of the best materials which provides a symmetrical superior strength and stiffness to structures. With the strengthening of people's environmental protection and resource reuse consciousness, the development of renewable materials, especially natural fiber-filled polymer composites, is receiving great attention. This study investigated the mechanical properties of polymer composites incorporating waste materials from the food processing industry and agricultural sources. Waste vegetal fiber-filled polymer biocomposites (WVFFPBs) with varying fiber types and 3D printing orientations were systematically fabricated. Subsequently, the tensile tests were executed to comprehensively assess the anisotropic mechanical behaviors of the WVFFPBs. The results demonstrated that WVFFPBs performed excellent anisotropic mechanical properties compared to pristine matrix samples as print orientation changed. As the printing angle increased from 0° to 90°, the tensile mechanical properties of the WVFFPBs displayed a decreasing trend. Moreover, the print orientation–anisotropic mechanical behavior relationship of 3D-printed WVFFPBs was revealed through the analysis of the material manufacturing characteristics and damage features. [ABSTRACT FROM AUTHOR]

The presented study is focused on the modification of commercially available epoxy resin with flame retardants by means of using natural substances, including quercetin hydrate and potato starch. The main aim was to obtain environmentally friendly material dedicated to rail transport that is resistant to the aging process during exploitation but also more prone to biodegradation in environmental conditions after usage. Starch is a natural biopolymer that can be applied as a pro-ecological filler, which may contribute to degradation in environmental conditions, while quercetin hydrate is able to prevent a composite from premature degradation during exploitation. To determine the aging resistance of the prepared materials, the measurements of hardness, color, mechanical properties and surface free energy were performed before and after solar aging. To assess the mechanical properties of the composite material, one-directional tensile tests were performed for three directions (0, 90, 45 degrees referred to the plate edges). Moreover, the FT-IR spectra of pristine and aged materials were obtained to observe the changes in chemical structure. Furthermore, thermogravimetric analysis was conducted to achieve information about the impact of natural substances on the thermal resistance of the achieved composites. [ABSTRACT FROM AUTHOR]

This study aims to fabricate eco-friendly fiber metal laminates (FMLs) with acceptable flexural and impact properties. For this reason, the jute and basalt fibers are hybridized into the epoxy matrix and then sandwiched between 2024 aluminum layers. After that, various contents of montmorillonite nanoparticles are dispersed in these structures to enhance these mechanical properties. To characterize the effect of hybridizing fibers and incorporating nanoparticles, macrostructural and microstructural investigations are performed. In hybrid structures, the highest flexural and impact properties are achieved, when the basalt layers are placed as exterior layers of the composite core. However, in the FMLs containing nanoclay particles, the FMLs with the 1.5 or 3 wt% nanoclay have an acceptable improvement in the mechanical properties, which relates to the exfoliated or intercalated structure of nanoclay. Creating nanocomposite interlocks on the surface of aluminum layers, enhancing the adhesion bonding at the interface of metal/composite, and improving the adhesion between jute or basalt fibers with the epoxy matrix are the distinct improving mechanisms, which are characterized by macro- and microstructural methods. [ABSTRACT FROM AUTHOR]

As an emerging science, tissue engineering and regenerative medicine focus on developing materials to replace, restore or improve organs or tissues and enhancing the cellular capacity to proliferate, migrate and differentiate into different cell types and specific tissues. Renewable resources have been used to develop new materials, resulting in attempts to produce various environmentally friendly biomaterials. Poly (lactic acid) (PLA) is a biopolymer known to be biodegradable and it is produced from the fermentation of carbohydrates. PLA can be combined with other polymers to produce new biomaterials with suitable physicochemical properties for tissue engineering applications. Here, the advances in modified PLA as tissue engineering materials are discussed in light of its drawbacks, such as biological inertness, low cell adhesion, and low degradation rate, and the efforts conducted to address these challenges toward the design of new enhanced alternative biomaterials. [ABSTRACT FROM AUTHOR]

The increasing concerns about plastic pollution and climate change have encouraged research into bioderived and biodegradable materials. Much attention has been focused on nanocellulose due to its abundance, biodegradability, and excellent mechanical properties. Nanocellulose-based biocomposites are a viable option to fabricate functional and sustainable materials for important engineering applications. This review addresses the most recent advances in composites, with a particular focus on biopolymer matrices such as starch, chitosan, polylactic acid, and polyvinyl alcohol. Additionally, the effects of the processing methods, the influence of additives, and the outturn of nanocellulose surface modification on the biocomposite's properties are outlined in detail. Moreover, the change in the composites' morphological, mechanical, and other physiochemical properties due to reinforcement loading is reviewed. Further, mechanical strength, thermal resistance, and the oxygen–water vapor barrier properties are enhanced with the incorporation of nanocellulose into biopolymer matrices. Furthermore, the life cycle assessment of nanocellulose and composites were considered to analyze their environmental profile. The sustainability of this alternative material is compared through different preparation routes and options. [ABSTRACT FROM AUTHOR]

This study focused on the development of a novel biocomposite material formed by a thermoplastic biodegradable polyester, poly(butylene succinate-co-adipate) (PBSA), and a carbonaceous filler as biochar (BC) derived by the pyrolysis of woody biomass waste. Composites with various BC contents (5, 10, 15, and 20 wt.%) were obtained by melt extrusion and investigated in terms of their processability, thermal, rheological, and mechanical properties. In all the composites, BC lowered melt viscosity, behaving as a lubricant, and enhancing composite extrudability and injection moulding at high temperatures up to 20 wt.% of biochar. While the use of biochar did not significantly change composite thermal stability, it increased its stiffness (Young modulus). Differential scanning calorimeter (DSC) revealed the presence of a second crystal phase induced by the filler addition. Furthermore, results suggest that biochar may form a particle network that hinders polymer chain disentanglement, reducing polymer flexibility. A biochar content of 10 wt.% was selected as the best trade-off concentration to improve the composite processability and cost competitiveness without compromising excessively the tensile properties. The findings support the use of biochar as a sustainable renewable filler and pigment for PBSA. Biochar is a suitable candidate to replace more traditional carbon black pigments for the production of biodegradable and inexpensive innovative PBSA composites with potential fertilizing properties to be used in agricultural applications. [ABSTRACT FROM AUTHOR]

The usage of new cellulosic fibers in industrial applications is massive because of its excellent performances. These fibers are utilized especially for manufacture of high-performance composites. Coconut leaf sheath (CLS) fibers are extracted for leaf sheath of coconut tree. The aim of this paper is to study the possibility of using a natural fiber CLS as an alternative for polymer composites. In the current study, the consequence of NaOH treatment on structural, thermal and morphological behavior of treated and untreated coconut leaf sheath (CLS) fiber in terms of single fiber tensile strength, Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (×RD), ther)mogravimetric analysis (TGA) and differential scanning calorimeter (DSC) has been explored. From SEM analysis, it was identified globular lumps spread consistently over the fiber which could help the mechanical interlock with the resin. The outcomes from the experimentation exposed that the NaOH treatment has impacted in the eradication of amorphous hemicellulose and lignin contents from the CLS fiber surface and in turn resulted in excellent structural and thermal stability behaviour of fiber. The present work endorses the great potential of CLS fibers to be utilized for bio-reinforcement in order to fabricate lightweight composite structures, employed in automobile and structural applications. [ABSTRACT FROM AUTHOR]

The impact of polymeric materials on the environment is a growing concern and an incentive for their commercial appeal. In composites, the trend is to replace matrices of synthetic polymers (SPs) with biopolymers (BPs) to develop bio‐based composites. The increasing demand for such materials has driven their research and application in many industrial sectors, often accompanied by increasingly restrictive fire safety regulations. With the aim of decreasing the flammability of composites, various approaches have been pursued, in particular the use of flame‐retardant (FR) additives. However, at high FR loads, the mechanical properties can be compromised. This article briefly overviews some aspects of the fire behavior and mechanical properties of BPs and bio‐based composites. Using a chart‐based framework and quadrant‐based quantitative analysis, the fire and mechanical properties of flame‐retarded composite formulations are evaluated simultaneously, aimed at comparing the effects of BPs and SPs in flame‐retarded polymeric composites in relation with other variables. [ABSTRACT FROM AUTHOR]

This work investigates the rheological behavior and characteristics of solutions and convened biopolymer films from Chitosan (Chi) modified by kombucha-derived bacterial cellulose (KBC). The Arrhenius equation and the Ostwald de Waele model (power-law) revealed that the Chi/KBC solutions exhibited non-Newtonian behavior. Both temperature and KBC concentration strongly affected their solution viscosity. With the selection of a proper solvent for chitosan solubilization, it may be possible to improve the performances of chitosan films for specific applications. The elasticity of the prepared films containing KBC 10% w/w was preferable when compared to the controls. FTIR analysis has confirmed the presence of bacterial cellulose, chitosan acetate, and chitosan lactate as the corresponding components in the produced biopolymer films. The thermal behaviors of the Chi (lactic acid)/KBC samples showed slightly higher stability than Chi (acetic acid)/KBC. Generally, these results will be helpful in the preparation processes of the solutions and biopolymer films of Chi dissolved in acetic or lactic acid modified by KBC powder to fabricate food packaging, scaffolds, and bioprinting inks, or products related to injection or direct extrusion through a needle. [ABSTRACT FROM AUTHOR]

Natural fibre biopolymer composites with both fibres and matrix being derived from biomaterials are increasingly used in demanding applications, such as sensing, packaging, building, and transport, and require good electrical, thermal, and flame retardant properties. Herein, an investigation of the effectiveness of functionalising nonwoven cotton/poly(lactic acid) (PLA) fibre mats with graphene oxide nanosheets has been reported by using a facile dip-coating method followed by thermal reduction for enhancing the electric, thermal, and abrasion-resistance properties. The manufacturing processes for preparing biocomposites and introducing functionality are readily scalable. Experimental results reveal that with the addition of less than 0.5 wt% graphene nanoplatelets, the biocomposites showed significant improvements in abrasion resistance, electrical conductivity, thermal conductivity, and diffusivity. Furthermore, the composite shows excellent piezo-resistivity to act as strain sensors with a gauge factor of 2.59 at strains up to 1%. [ABSTRACT FROM AUTHOR]

Edible films and coatings are edible thin layers used as food coatings or barriers between foods and the environment. Biopolymers including polysaccharides, proteins or their mixture which used to produce edible films, are high potential as carriers of additives such as anti-microbial agents and antioxidants. Generally, the use of edible and biodegradable films has been limited due to their sensitivity to moisture and poor mechanical properties. On the other side, the use of a combination of polymers for film forming considered as an effective method to overcome mentioned limitations, so, the best functional properties of each compound can be used.This paper intended to investigate the ability of the mucilage from chia seeds in combination with gelatin to form a suitable composite film and produce a new type of biodegradable biopolymers used in food packaging. Chitosan nanoparticles used in four different levels (0, 2, 4 and 6%) as antimicrobial agent in the production of the films. Physicochemical and antimicrobial properties of the produced films were evaluated. Results shown that adding chitosan nanoparticles in different percentages caused significant changes in water vapor permeability (0.129- 256), opacity (0.656–6.185), ΔE colorimetric factor (5.570–4.736) and antimicrobial properties against gram-positive microorganisms (S. aureus) (1-21.666 mm) (p < 0.05). Furthermore, the microbial tests indicated a greater inhibitory effect of chitosan nanoparticles against gram-positive bacteria (max for gram positive = 21.666 mm vs. max for gram negative = 12.333 mm). In conclusion, development of the environmental friendly food packaging such as bio-composite or nanobiocomposite ones reduces the negative impacts of packaging on the environment. Although nanocomposites are an improved form of biopolymers, they still have some deficiencies compared to synthetic polymers that limit their use. To overcome these drawbacks, various agricultural and food-based materials should be considered and evaluated for their potential application in the packaging industry. [ABSTRACT FROM AUTHOR]

The use of biopolymers for tissue engineering has recently gained attention due to the need for safer and highly compatible materials. Starch is one of the most used biopolymers for membrane preparation. However, incorporating other polymers into starch membranes introduces improvements, such as better thermal and mechanical resistance and increased water affinity, as we reported in our previous work. There are few reports in the literature on the biocompatibility of starch/chicken gelatin composites. We assessed the in vivo biocompatibility of the five composites (T1–T5) cassava starch/gelatin membranes with subdermal implantations in biomodels at 30, 60, and 90 days. The FT-IR spectroscopy analysis demonstrated the main functional groups for starch and chicken gelatin. At the same time, the thermal study exhibited an increase in thermal resistance for T3 and T4, with a remaining mass (~15 wt.%) at 800 °C. The microstructure analysis for the T2–T4 demonstrated evident roughness changes with porosity presence due to starch and gelatin mixture. The decrease in the starch content in the composites also decreased the gelatinization heats for T3 and T4 (195.67, 196.40 J/g, respectively). Finally, the implantation results demonstrated that the formulations exhibited differences in the degradation and resorption capacities according to the starch content, which is easily degraded by amylases. However, the histological results showed that the samples demonstrated almost complete reabsorption without a severe immune response, indicating a high in vivo biocompatibility. These results show that the cassava starch/chicken gelatin composites are promising membrane materials for tissue engineering applications. [ABSTRACT FROM AUTHOR]

The growing awareness of socioeconomic and environmental issues and the high percentage of petroleum resources consumed and new environmental regulations have fueled efforts to develop innovative, cutting-edge, environmentally friendly materials with a wide range of applications. Due to environmental and sustainability concerns, the advancement of biocomposites has resulted in tremendous breakthroughs in green materials in this century. Their primary goal is to replace current synthetic petroleum-based composites with natural resources. Materials derived from nonrenewable petroleum-based sources are hazardous and expensive to produce; on the other hand, biocomposites derived from natural sources are biodegradable, recyclable, non-abrasive, and compostable and have properties comparable to synthetic fiber composites. Natural fibers are low-cost, lightweight, biodegradable, renewable, and environmentally friendly alternatives to synthetic fibers like glass and carbon fiber. The long-term viability of natural fiber-based composite materials has led to increased use in various production industries. However, the manufacturing process of natural fiber-based biocomposites is still plagued by some difficulties, such as poor adhesive propensity, moisture absorption, poor fire resistance, low impact strength, and low durability. This review provides a panoramic view to provide insight into different aspects of biocomposites based on natural fibers and polymers in terms of properties and applications, which will pave the way for future biocomposites research in academic and commercial contexts. [ABSTRACT FROM AUTHOR]

Polymers are synonymous with the modern way of living. However, polymers with a large carbon footprint, especially those derived from nonrenewable petrochemical sources, are increasingly perceived as detrimental to the environment and a sustainable future. Polyhydroxyalkanoate (PHA) is a microbial biopolymer and a plausible alternative for renewable sources. However, PHA in its monomeric forms has very limited applications due to its limited flexibility, tensile strength, and moldability. Herein, the life cycle of PHA molecules, from biosynthesis to commercial utilization for diverse applications is discussed. For clarity, the applications of this bioplastic biocomposite material are further segregated into two domains, namely, the industrial sector and the medical sector. The industry sectors reviewed here include food packaging, textiles, agriculture, automotive, and electronics. High-value addition of PHA for a sustainable future can be foreseen in the medical domain. Properties such as biodegradability and biocompatibility make PHA a suitable candidate for decarbonizing biomaterials during tissue repair, organ reconstruction, drug delivery, bone tissue engineering, and chemotherapeutics. [ABSTRACT FROM AUTHOR]

Raising environmental awareness had forced researchers to explore the potential and implementation of environmentally friendly materials as alternatives for conventional materials. Environmentally friendly materials are biodegradable, safer, non-toxic, lightweight, cheap, and readily available. Arrowroot starch has a high content of amylose (~35.20%) which makes it suitable for better film production. Starch extracted from arrowroot rhizomes can be blended, plasticized with other polymers, or reinforced with fibres to improve their properties. The melt blended glycidyl methacrylate-grafted polylactide (PLA-g-GMA) and treated arrowroot fiber (TAF) treated with coupling agent developed PLA-g-GMA/TAF composite, which showed better properties than the PLA/AF composite. To the best of our knowledge, no comprehensive review paper was published on arrowroot fibres, starch biopolymer, and its biocomposites before. The present review focuses on recent works related to the properties of arrowroot fibres and starch, and their fabrication as biocomposites. The review also reveals the vast potential of arrowroot fibres and starch for food industries, medicines, textiles, biofuel, pulp, and paper-making industries, bioenergy, packaging, automotive, and many more.

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]

High-power laser irradiation interaction with natural polymers in biocomposites and Laser-Induced Chitin Deacetylation (LICD) was studied in this work, in order to produce thin films consisting of chitosan composite. The new method can lead to a cutting-edge technology, as a response to the concern regarding the accumulation of "natural biological waste" and its use. The process consists of high-power laser irradiation applied on oyster shells as the target and deposition of the ablated material on different substrates. The obtained thin films we analyzed by FTIR, UV-VIS and LIF spectroscopy, as well as SEM-EDS and AFM. All the results indicated that chitin was extracted from the shell composite material and converted to chitosan by deacetylation. It was, thus, evidenced that chemical transformation in the chitin polymer side-chain occurs during laser irradiation of the oyster shell and in the resulted plasma plume of ablation. The numerical simulation in COMSOL performed for this study anticipates and confirms the experimental results of chitin deacetylation, also providing information about the conditions required for the physico-chemical processes involved. The high sorption properties of the thin films obtained by a LICD procedure is evidenced in the study. This quality suggests that they should be used in transdermal patch construction due to the known hemostatic and antibacterial effects of chitosan. The resulting composite materials, consisting of the chitosan thin films deposited on hemp fabric, are also suitable for micro-filters in water decontamination or in other filtering processes. [ABSTRACT FROM AUTHOR]

This review addresses the current trend of replacing petroleum-based polymers in food packaging with bio-based alternatives, specifically focusing on proteins and polysaccharides. While these biopolymers exhibit excellent film-forming properties and are abundant in nature, their individual use in packaging lacks ideal plastic-like characteristics, especially in terms of mechanical and barrier properties. A recent solution involves the formulation of biocomposites through the reinforcement of one biopolymer with another (e.g., protein with a polysaccharide), significantly enhancing the physical, mechanical, and barrier properties of packaging materials. The review concentrates on the integration of proteins and polysaccharides in biocomposite materials, emphasizing their potential applications in active and intelligent food packaging systems. It covers sources, manufacturing methods, interaction mechanisms, recent developments, perspectives, and opportunities. The exploration extends to practical implementations of these biocomposites in enhancing food quality, safety, and shelf life—a green technological approach contributing to the reduction of food waste and loss. [Display omitted] [ABSTRACT FROM AUTHOR]

This study focused on the development of a novel biocomposite material formed by a thermoplastic biodegradable polyester, poly(butylene succinate-co-adipate) (PBSA), and a carbonaceous filler as biochar (BC) derived by the pyrolysis of woody biomass waste. Composites with various BC contents (5, 10, 15, and 20 wt.%) were obtained by melt extrusion and investigated in terms of their processability, thermal, rheological, and mechanical properties. In all the composites, BC lowered melt viscosity, behaving as a lubricant, and enhancing composite extrudability and injection moulding at high temperatures up to 20 wt.% of biochar. While the use of biochar did not significantly change composite thermal stability, it increased its stiffness (Young modulus). Differential scanning calorimeter (DSC) revealed the presence of a second crystal phase induced by the filler addition. Furthermore, results suggest that biochar may form a particle network that hinders polymer chain disentanglement, reducing polymer flexibility. A biochar content of 10 wt.% was selected as the best trade-off concentration to improve the composite processability and cost competitiveness without compromising excessively the tensile properties. The findings support the use of biochar as a sustainable renewable filler and pigment for PBSA. Biochar is a suitable candidate to replace more traditional carbon black pigments for the production of biodegradable and inexpensive innovative PBSA composites with potential fertilizing properties to be used in agricultural applications.

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]

Being credited with the most extensively studied polysaccharide polymer and promising candidate for versatile applications, chitosan has proved to be a standalone material with loads of diversified properties in various structural forms such as blends and composites. Considering the abundance of this biopolymer and its non-toxic nature, exploiting chitosan offers two-folded benefits – environment friendliness and fabrication as per the need. Alkaline deacetylation of chitin produces chitosan as a polymer that can be tuned to a great extent as per the requirement by altering the degree of deacetylation (DDA) and molecular weight (MW). This biopolymer has been widely investigated for potential application in the food and biomedical fields due to its antimicrobial and antibacterial properties. Chitosan based composite films incorporated with different natural extracts have shown significant enhancement in the physical and biological activities as reported by different studies. The current study reviews recent developments and investigations of chitosan based biocomposite films incorporated with different natural extracts emphasizing on the improvement of physical and biological properties and its applications. [ABSTRACT FROM AUTHOR]

In this era of green and sustainable manufacturing, natural fibre-reinforced polymer composites (NFPC) have been widely accepted as the potential alternatives for polymer matrix composites (PMC) or any other non-biodegradable composites. Despite the increasing need to replace plastic bottles, bags, disposable plastic plates and trays, seedling pots used in our day to day life, not many studies have been made in this direction. The current work aims at developing a hundred percent biodegradable composite by reinforcing waste Kibisu silk fibre into wheat gluten as a possible replacement of plastic disposables. The developed composites are made up of different mass fractions of Kibisu silk fibre reinforced into plasticised wheat gluten. The prepared composites have been characterised to obtain the best combination. The developed composites were found to have adequate tensile property, mass degradation at a considerably high temperature and most importantly, the outstanding rate of biodegradation under normal atmospheric conditions. The soil quality test before and after degradation also showed no significant changes in the quality of the soil. FTIR studies revealed improved interaction between wheat gluten, glycerol and Kibisu fibres upon addition of natural lemon extract as crosslinker. Overall results indicate that the developed biocomposites have the potential to substitute harmful plastic disposables like plastic seedling pots and plates, disposable hospital tray, dustbin, etc. [ABSTRACT FROM AUTHOR]

Purpose: The objective of the present study was to better understand the potential environmental benefit of using vine shoots (ViShs), an agricultural residue, as filler in composite materials. For that purpose, a comparative life cycle assessment (LCA) of a rigid tray made of virgin poly(3-hydroxybutyrate-co-3-hydroxyvalerate) PHBV, polylactic acid (PLA) or polypropylene (PP), and increasing content of ViSh particles was performed. The contribution of each processing step in the life cycle on the different environmental impacts was identified and discussed. Furthermore, the balance between the environmental and the economic benefits of composite trays was discussed. Methods: This work presents a cradle-to-grave LCA of composite rigid trays. Once collected in vineyards, ViShs were dried and ground using dry fractionation processes, then mixed with a polymer matrix by melt extrusion to produce compounds that were finally injected to obtain rigid trays for food packaging. The density of each component was taken into account in order to compare trays with the same volume. The maximum filler content was set to 30 vol% according to recommendations from literature and industrial data. The ReCiPe 2016 Midpoint Hierarchist (H) methodology was used for the assessment using the cutoff system model. Results and discussion: This study showed that bioplastics are currently less eco-friendly than PP. This is in part due to the fact that LCA does not account for, in existing tools, effects of microplastic accumulation and that bioplastic technologies are still under development with low tonnage. This study also demonstrated the environmental interest of the development of biocomposites by the incorporation of ViSh particles. The minimal filler content of interest depended on the matrices and the impact categories. Concerning global warming, composite trays had less impact than virgin plastic trays from 5 vol% for PHBV or PLA and from 20 vol% for PP. Concerning PHBV, the only biodegradable polymer in natural conditions in this study, the price and the impact on global warming are reduced by 25% and 20% respectively when 30 vol% of ViSh are added. Conclusion: The benefit of using vine shoots in composite materials from an environmental and economical point of view was demonstrated. As a recommendation, the polymer production step, which constitutes the most important impact, should be optimized and the maximum filler content in composite materials should be increased. [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.

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.

Gelatine is a biocompatible and natural polymer with chemical properties similar to the extracellular matrix. However, it has poor mechanical properties and sensitive to enzymatic biodegradation that limits its application in 3D scaffold fabrication. Cellulose nanofibrous (CNF) offers biocompatibility, high surface area and excellent mechanical properties with slow in-vivo degradation. To fine tune their properties, CNF, and gelatine (CNF-GEL) were blended to form biocomposite aerogels. Epichlorohydrin (EPH) was incorporated into CNF-GEL as a chemical crosslinker to investigate its effect on the physiochemical, mechanical, and biological properties of the biocomposite aerogels both in-vitro and in-vivo. Regardless of the composition of the prepared aerogels, they possessed porosity of >90% with the pore size of 7–135 μm, which was confirmed in the morphological analysis. The presence of EPH improved the chemical interaction between CNF and gelatine, hence enhanced the compressive strength compared to uncrosslinked samples. The formulation of crosslinked CNF-GEL 90:10 offered the highest compressive strength of 61.35 kPa. The in-vitro and in-vivo studies showed adequate cytocompatibility, cell viability and cell attachment in the optimal crosslinked formulation with tuned enzymatic degradation. Antimicrobial property was also achieved in the optimal scaffold by incorporating curcumin as an antimicrobial agent. [ABSTRACT FROM AUTHOR]

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In the present study, a magnetically separable potent solid acid nanocatalyst with a facile preparation technique was fabricated via incorporation of fibroin as a natural polymer with Fe3O4 nanoparticles. In fact, the Fe3O4 nanoparticles were thoroughly covered by the fibroin protein, followed by treating with chlorosulfuric acid for surface sulfonation. Next, physicochemical properties were characterized using FT-IR, XRD, TGA, SEM, EDX, and TEM techniques to elucidate the Fe3O4@fibroin-SO3H structure. The analyses proved the core–shell structure and the presence of sulfonyl on the surface. The Fe3O4@fibroin-SO3H showed significant activity in the tetrazole derivatives synthesis reactions under solvent-free and relatively mild conditions. The structure of the products was validated using 1H-NMR and 13C-NMR. The prepared catalyst showed good stability and reusability even after easy separation by an external magnet for four consecutive reaction rounds. Considering the crucial importance of sulfuric acid catalysis, we believe that Fe3O4@fibroin-SO3H will find wide applications as a separable, green, and potent solid acid nanocatalyst. [ABSTRACT FROM AUTHOR]

Polymeric biocomposites (Polyaniline/sugarcane bagasse (Pan/SB), polypyrrole (PPy/SB), polyaniline/chitosan (PAn/Ch), polyaniline/starch (PAn/St) and polypyrrole/starch (PPy/St)) were prepared and applied for Acid Black-234 (AB-234) dye removal as a function of pH, reaction time, adsorbent dose, initial dye concentration and temperature. The optimum pH for the efficient adsorption for SB, PPy/SB, PAn/SB, PPy/Ch, PAn/Ch, PPy/St and PAn/St were 2, 3, 4, 4, 5, 3 and 3, respectively using adsorbent dose of 0.05 g for the reaction time of 60 min. The pseudo-first-order-kinetic model better explained the biosorption processes of SB, PAn/SB, PAn/Ch, PPy/St and PAn/St, while pseudo-second-order kinetic model better fitted to the kinetic data of PPy/SB and PPy/Ch. It was observed that the biosorption process of dye showed the satisfactory fitness for Langmuir isotherm for the biosorbents with maximum adsorption capacities 52.6, 100, 90.91, 90.0, 71.4, 66.6 and 62.5 for SB, PPy/SB, PAn/SB, PPy/Ch, PAn/Ch, PPy/St and PAn/St, respectively. The thermodynamic study revealed the exothermic nature of adsorption of dye on to biocomposites. Results revealed that polymeric biocomposites are efficient adsorbent and could possibly be used for the adsorption of dyes from textile wastewater. • Chitosan, starch, polyaniline and polypyrrole composites were prepared with sugarcane bagasse. • Composites were characterized and used for the adsorption of Acid Black-234 dye. • Dye adsorption followed the pseudo-first-order-kinetic model and Langmuir isotherm • The biocomposites have potential to remove dye from textile wastewater [ABSTRACT FROM AUTHOR]

Pelletized biomaterial composites that contain chitosan (C) and torrefied wheat straw (S) at variable weight composition (C:S) were prepared using a facile blending process. The fractional content of the wheat straw was studied to elucidate the role of biomass on the pelletized product and effects of S-content on the physicochemical properties relevant to adsorption phenomena. Chitosan pellets (with and without S) were characterized by spectroscopic (FT-IR and 13C NMR) and thermal (TGA and DSC) techniques to provide support for their respective C:S composition. Confocal microscopy using fluorescein (FL) as a dye probe revealed the presence and an increase in the accessibility of the active sites for the composite pellets according to the S-content (wt %). Equilibrium and kinetic sorption studies using FL and reactive black (RB) dyes revealed an incremental adsorption affinity of the pellets with anionic dyes in variable charge states (FL and RB). The trend for dye adsorption parallels the incremental S-content (wt %) in the composite pellets. This study reports a first-example of a low-cost, facile, and sustainable approach for the valorization of straw and chitosan suitable for sorption-based applications in aqueous media. [ABSTRACT FROM AUTHOR]

This study analysed the possibilities of developing biocomposites using a combination of poly lactic acid and polybutylene adipate terephthalate combined with micro cellulose from four different agricultural residues (banana pseudo stem, screw pine, pineapple leaf, and water hyacinth) in various combinations to produce biodegradable kitchenware suitable for food serving, consumption and other culinary applications. Tensile strength of developed composites varied between 14 and 18 MPa. Crystallinity of the samples varied between 26 % and 50 %. Contact angle results (47–83°) exposed the hydrophilic nature of the developed biocomposite. The results were analysed to optimise the mould and injection moulding procedure parameters. The analysis of the developed kitchenware indicated minimal water absorption and leaching, suitable for culinary application. Biodegradability tests indicated complete degradation of samples within 80 days. All samples indicated comparable results, with pineapple leaf-based samples exhibiting better characteristics. The experiment demonstrates the effectiveness of developed kitchenware as an effective solution for the present environmental issues caused by the disposal of single-use non-biodegradable plastic-based kitchenware. [Display omitted] • Agri biomass based micro cellulose blended with biopolymer to produce biodegradable kitchenware for food serving. • By using compression with injection mechanism to optimised the production process • The developed bio composite had impressive mechanical, water barrier properties and degraded around 80days • Among the selected micro cellulose pineapple leaf-based bio composite exhibiting better all the characteristics. [ABSTRACT FROM AUTHOR]

• Preparing biocomposites of ciprofloxacin- montmorillonite/ N,N,N- triethyl chitosan via simple method. • Using Na+ montmorillonite not only as an adsorbent of ciprofloxacin but also as a carrier. • Replacing antibiotic with N,N,N- triethyl chitosan as both a natural polymer and a coating for biocomposite. In this work, in order to prepare biocomposites of ciprofloxacin- montmorillonite/ N,N,N- triethyl chitosan (CMC/TEC and CMC׳/TEC), ciprofloxacin was intercalated into the Na+-montmorillonite layers in two different pHs and coated with N,N,N- triethyl chitosan. XRD and FT-IR data demonstrated that ciprofloxacin (CIP) diffused among the layers of montmorillonite. The prepared biocomposites were further characterised by TG, SEM, BET, DSC, and disk diffusion method to investigate antibacterial activity against Staphylococcus aureus as well. Coated composites with N,N,N- triethyl chitosan possessed efficiency of the drug encapsulation, and controlled the release of drug from the biocomposites in comparison with composites without N,N,N- triethyl chitosan. Study of antibacterial activities of two biocomposites of CMC1/TEC and CMC2/TEC with lower release rates and lower concentrations of CIP than other biocomposites revealed that likely N,N,N- triethyl chitosan could considerably help to reduce the consumption of ciprofloxacin. By doing more researches on other bacterial strains and performing advanced tests on our own biocomposites, N,N,N- triethyl chitosan can probably be proved as a suitable candidate for a substitute in biomedical activities. [ABSTRACT FROM AUTHOR]

Abstract This work deals with provision and characterization of the biopolymer-based composites achieved by incorporation of cellulose fibers as the reinforcement within the glycerol plasticized matrix formed by thermoplastic cornstarch biopolymer. The function of starch-based polymers is limited due to poor mechanical properties. However, it is improved with forming a biocomposite of thermoplastic starch (TPS) as matrix and the cellulose fibers (CF) as reinforcement. The surface of cellulose fibers is successfully modified using the air plasma treatment with the aim of improving the matrix/fiber adhesion. The modified fibers are studied using X-ray diffraction (XRD), scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The TPS/CF composites are prepared using high friction and hot compression procedure. Tensile test results and SEM images of the fracture surfaces show significant improvement of adhesion between treated cellulose fibers and TPS matrix. Thermogravimetric analysis shows a considerable decomposition at approximately 250–350 °C. XRD proved the significant increase in crystallinity percentage of composites compared to TPS. [ABSTRACT FROM AUTHOR]

In this work, agave fibers were surface treated using maleated PLA (MAPLA) in order to increase the fiber content (from 10 up to 40% wt.) in polylactic acid (PLA) biocomposites produced by rotational molding and to study the effect of the agave fiber and its treatment on the physical, mechanical and thermal properties of the biocomposites. This chemical modification between agave fibers and MAPLA was evaluated by FTIR spectroscopy. In general the results indicate that MAPLA surface treatment produces a more homogeneous morphology with lower interfacial gaps and overall porosity, especially at higher agave contents. This improved compatibility promoted better stress transfer leading to increased mechanical properties. For example, the tensile strength and modulus of treated fiber composites increased by up to 68% (from 25 to 41 MPa) and 32% (from 1.30 to 1.74 GPa) respectively, in comparison with untreated fiber composites. Fiber surface treatment also decreases hydrophilicity, lowering water absorption and diffusion coefficient. From thermo-mechanical analyses, the damping behavior of the biocomposites decreased with MAPLA treatment since a stronger interface is able to sustain higher stresses and dissipates less energy. Finally, the thermal stability was also improved as a result of better interfacial chemical bonding leading to a 12 °C increase in thermal stability (from 254 to 266 °C). [ABSTRACT FROM AUTHOR]

Graphical abstract Highlights • The biopolymer-based from cassava starch (CS) and cellulose fiber (CF) from sugar cane leave was made by help of carboxylated styrene-butadiene rubber (CSBR) as an adhesion. • The addition of the cellulose fiber in the CSBR/CS blend exhibited higher in tensile strength compared to unfilled CF sample. • This study demonstrated a significant concentration of the CF improved the film properties. • The inexpensive biodegradable film was expected to be a promising candidate for alternative packaging materials. Abstract The biopolymer-based from cassava starch (CS) and cellulose fiber (CF) from sugar cane leaves was prepared by help of carboxylated styrene-butadiene rubber (CSBR) as an adhesion. The CF was isolated by using acid hydrolysis under heating (50 wt%, 140 °C for 2 h). The size, morphology, chemical structure, interaction bonding, dynamic mechanical behavior, thermal analysis, biodegradation, physical and mechanical performance of CSBR/CS/CF composites were investigated. The highest tensile value was found at 1.6 wt% CF loading (27.96 MPa) while preserving the large extent of their biodegradability (<80% after buried in soil for 30 days). Moreover, the increasing CF content led to decrease in the water contact angle, moisture content owing to the interfacial adhesion between carboxyl groups on the CSBR and hydroxyl groups on the CF surfaces. This study demonstrated a significant concentration of the CF on film properties. Moreover, these inexpensive biodegradable composites were preferable for packing, fruit container and paper coating applications. [ABSTRACT FROM AUTHOR]

Abstract: In this work, films based on bacterial cellulose nanofibers (BCNFs) incorporating gelatin hydrolysate (GH) from tilapia skin were produced. The effect of plasticizer (sorbitol or glycerol) and GH incorporation was evaluated on the physical-chemical and optical properties of films. BCNFs were produced using bacterial cellulose obtained from Hestrin and Schramm (HS) medium (BCNF-HS) or cashew apple juice (BCNF-CM), which was studied as an alternative to HS. Films with sorbitol showed the best properties and were selected for further characterization, using 40% (w/w) of BCNF-HS, 40% (w/w) of GH and 20% (w/w) of sorbitol (BCNF-HS-S-GH films). These films exhibited an antioxidant activity of 7.8 µmols Trolox Eq/g film, a water vapor permeability (WVP) of 1.6 g.mm/kPa.h.m2 and an Young’s modulus of 0.57 GPa. Films produced with BCNFs obtained from cashew apple juice revealed enhanced tensile strength, elongation at break, and thermal stability. Caco-2 cells’ viability after incubation with BCNF-based films incorporating GH was evaluated and showed non-cytotoxicity, reinforcing the safety of the developed materials and their potential use in food applications.Graphical abstract: [ABSTRACT FROM AUTHOR]

The current study deals with the preparation and characterization of polysaccharide‐based biocomposite films acquired by the incorporation of cellulose nanofiber within glycerol plasticized matrix formed by starch. The application of starch‐based films is restricted owing to highly hydrophilic nature and poor mechanical properties. These problems are solved by forming a nanocomposite of thermoplastic starch (TPS) as matrix and cellulose nanofiber (CNF) as reinforcement. CNF is successfully synthesized from short pure cellulose fibers by a chemo‐mechanical process. TPS/CNF composite films are prepared by the polymer solution casting method, and their characterizations are obtained by water vapor transmission rate, differential scanning calorimetry (DSC), atomic force microscopy (AFM), oxygen transmission rate, X‐ray diffraction (XRD), light transmittance, and tensile test. Even at the low concentration of CNF filled TPS, the composite film shows improvement in properties. The 0.4 wt% CNF loaded TPS films show approximately the maximum improvement in tensile strength. Above 0.5 wt% CNF, tensile strength starts to deteriorate. Water vapor transmission rate (WVTR) and oxygen transmission rate (OTR) results show improvement in water vapor barrier properties of TPS matrix. The DSC thermograms of TPS and composite films do not show any significant effect on the melting point of the composite film compared with the base polymer TPS. The AFM analysis shows the topography of the surface of the nanocomposite. The morphology of nanofibers is studied by using the scanning electron microscopy (SEM) and the transmission electron microscopy (TEM). [ABSTRACT FROM AUTHOR]

Nano-hydroxyapatite (nHAp), surface functionalized with linear polyethylenimine (LPEI), was used for the preparation of biocomposites in combination with biopolymers and poly(ε-caprolactone) (PCL), by cryogelation technique, to yield biomimetic scaffolds with controlled interconnected macroporosity, mechanical stability, and predictable degradation behavior. The structural characteristics, swelling and degradation behavior of hydroxyapatite and hydroxyapatite/β-tricalcium phosphate (β-TCP) filled matrices were investigated as compared to the corresponding naked polymer 3D system. It was found that the homogeneity and cohesivity of the composite are significantly dependent on the size and amount of the included inorganic particles, which are thus determining the structural parameters. Surface modification with LPEI and nanodimensions favored the nHAp integration in the organic matrix, with preferential location along protein fibers, while β-TCP microparticles induced an increased disorder in the hybrid system. The biocomposite including nHAp only was further investigated targeting biomedical uses, and proved to be non-cytotoxic and capable of acting as gene-activated matrix (GAM). It allowed sustained delivery over time (until 22 days) of embedded PEI 25 -pDNA polyplexes at high levels of transgene expression, while insuring a decrease in cytotoxicity as compared to polyplexes alone. Experimental data recommend such biocomposite as an attractive material for regenerative medicine. [ABSTRACT FROM AUTHOR]

Disposable containers made of non-biodegradable polymers are considered as one of the most prevalent environmental pollutants. It is very important and desirable to make fully biodegradable disposable containers for food packaging that does not endanger the health of consumers. In this research, fully biodegradable polymer composites were prepared by melt mixing of polylactic acid (PLA), polybutylene succinate (PBS), and natural polymers including corn starch and wheat straw, and their physical and mechanical properties were evaluated. For this purpose, by conducting experiments according to the optimal custom mixture design of the response surface methodology, the effect of 3 independent variables including the concentration of the PLA and PBS biopolymers blend (50/50% w/w) (CBB) in the range of 30–70, the concentration of corn starch (CCS) in the range of 30–60 and the concentration of wheat straw (CWS) in the range of 0–8 wt percentage of biocomposite on the dependent variables including the elastic modulus (EM), elongation at break (EB), impact strength (IS) and equilibrium moisture content (EMC) of the biocomposite sheet were investigated. According to the results of this research, with the increase in the concentration of corn starch and wheat straw in the studied range, the EM and EMC of the biocomposite increased, while its EB and IS decreased. According to the results obtained from optimizing the effects of independent variables on the physicomechanical properties of the biocomposite sheet, the optimal values predicted by the models for CBB, CCS and CWS were 48.2 wt%, 45.4 wt%, and 6.4 wt%, respectively and predicted values for EM, EB, IS and EMC were 80.8 MPa, 11.4%, 2 kJ/m2 and 4.1%, respectively. Also, the biodegradability rate of the biocomposite with the optimal formulation was 71.1% in the fifth month of the test. • Biocomposites of biopolyester blend filled with two natural polymers were prepared. • Biocomposites contained polylactic acid, polybutylene succinate, starch, and wheat straw. • Constituents concentration had main effects on the sheet's physicomechanical properties. • Optimal sheet contains 48.2 wt% biopolyester blend and 51.8 wt% natural polymers. • The biocomposite sheet with optimal formulation had a high degree of biodegradability. [ABSTRACT FROM AUTHOR]