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Cellulosic fibers obtained from Barley straw were utilized to reinforce PHB. Four different processed fibers were employed as reinforcing material: sawdust (SW), defibered (DFBF), delignified (DBF), and bleached (BBF) fibers. The composite was processed from two different perspectives: a discontinuous (bach) and an intensification process (extrusion). Once processed and transformed into final shape specimens, the materials were characterized by mechanical testing (tensile mode), scanning electron microscopy, and theoretical simulations by finite elements analysis (FEA). In terms of mechanical properties, only the elastic moduli (Et) exhibited results ranging from 37% to 170%, depending on the reinforcement composition. Conversely, strengths at break, under both tensile and bending tests, tended to decrease, indicating poor affinity between the components. Due to the mechanical treatment applied on the fiber, DFBF emerged as the most promising filler, with mechanical properties closest to those of neat PHB. DFBF-based composites were subsequently produced through process intensification using a twin-screw extruder, and molded into flowerpots. Mechanical results showed almost identical properties between the discontinuous and intensification processes. The suitability of the material for agriculture flowerpots was demonstrated through finite analysis simulation (FEA), which revealed that the maximum von Mises stresses (5.38 × 105 N/m2) and deformations (0.048 mm) were well below the limits of the composite materials. [ABSTRACT FROM AUTHOR]

Disposable surgical gowns are usually made from petroleum-based synthetic fibers that do not naturally decompose, impacting the environment. A promising approach to diminish the environmental impact of disposable gowns involves utilizing natural fibers and/or bio-based synthetic fibers. In this study, composite webs from polylactic acid (PLA) bicomponent fiber and natural fibers, cattail and kapok fibers, were prepared using the hot press method. Only the sheath region of the PLA bicomponent fiber melted, acting as an adhesive that enhanced the strength and reduced the thickness of the composite web compared with its state before hot pressing. The mechanical and physical properties of these composite webs were evaluated. Composite webs created from kapok fibers displayed a creamy yellowish-white color, while those made from cattail fibers showed a light yellowish-brown color. Additionally, the addition of natural fibers endowed the composite webs with hydrophobic properties. The maximum natural fiber content, at a ratio of 30:70 (natural fiber to PLA fiber), can be incorporated while maintaining proper water vapor permeability and mechanical properties. This nonwoven material presents an alternative with the potential to replace petroleum-based surgical gowns. [ABSTRACT FROM AUTHOR]

In this study, we utilized a hybridization approach for two different fibers to overcome the drawbacks of single-fiber-reinforced PLA composites. Coir fiber and bamboo leaf fiber were used as reinforcing natural fibers as their properties complement one another. Additionally, we combined thermal annealing with hybridization techniques to further improve the overall properties of the composites. The results showed that the hybridization of BF: CF with a ratio of 1:2 gave PLA-based hybrid composites optimal mechanical and thermal properties. Furthermore, the improvement in the thermal stability of hybrid composites, attributable to an increase in crystallinity, was a result of thermal annealing. The improvement in HDT in annealed 1BF:2CF hybrid composite was about 13.76% higher than that of the neat PLA. Annealing of the composites led to increased crystallinity, which was confirmed using differential scanning calorimetry (DSC). The synergistic effect of hybridization and annealing, leading to the improvement in the thermal properties, opened up the possibilities for the use of PLA-based composites. In this study, we demonstrated that a combined technique can be utilized as a strategy for improving the properties of 100% biocomposites and help overcome some limitations of the use of PLA in many applications. [ABSTRACT FROM AUTHOR]

The effect of the chemical treatment of paper mill sludge fibers and polypropylene molecular weight were studied relative to the physical, mechanical, and morphological properties of a novel cellulosic biocomposite. Paper mill sludge fibers were treated with acetic anhydride, and succinic anhydride was mixed with maleic anhydride polypropylene (MAPP) and coupling agent (0 and 3%). The ratio of fibers and polymer materials was considered 30 to 70, which was manufactured by the hotpressing method at 180 °C. Water absorption, volume swelling, and contact angle were examined on each specimen according to ASTM standards, while Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) explored the efficiency of chemical modification of fibers and the morphology of biocomposites, respectively. The results showed that chemical treatment of fibers reduced the water absorption and volumetric swelling. Both tensile and flexural strength were increased with chemical treatment using the coupling agent. Comparison of fibers treated with succinic acid and acetic acid showed that the succinic acid enhanced the mechanical properties better than the acetic acid treatment. Finally, FTIR analysis showed that the hydroxyl groups decreased, and SEM images indicated the interface between fibers and polypropylene improved via chemical treatment of sludge fibers. [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]

A new class of biobased composites with tailorable mechanical properties made of natural fibers, polylactic acid, and ferulic acid derivatives (FAD) is studied. FAD was used to develop composites with elastomeric properties like improved elongation at break and highly reversible deformation upon elongation. Composites were prepared using raw and enzymatically treated hemp fibers. The fibers were defibrillated due to the enzymatic treatment increasing their aspect ratio. The composites were characterized by their mechanical properties and their reaction to fire. No significant change in the dispersion of the fibers in the composites was reported. Homogenously dispersed crystallites of FAD were observed by scanning electron microscopy in the PLA matrix and at the interface between the PLA and the fibers, where they are suspected to increase the free volume in correlation with a decrease in mechanical properties following the increase in the aspect ratio of the fibers. FAD also degraded the reaction to fire of the material with an increase in 10% of the peak of Heat Release Rate (pHRR) in comparison to neat PLA. It also increased the charring residue up to 3 wt.%. A synergistic effect between FAD and the lignin increasing the charring residue is also reported. [ABSTRACT FROM AUTHOR]

The development of new materials is currently focused on replacing fossil-based plastics with sustainable materials. Obtaining new bioplastics that are biodegradable and of the greenest possible origin could be a great alternative for the future. However, there are some limitations—such as price, physical properties, and mechanical properties—of these bioplastics. In this sense, the present work aims to explore the potential of lignin present in black liquor from paper pulp production as the main component of a new plastic matrix. For this purpose, we have studied the simple recovery of this lignin using acid precipitation, its thermoplastification with glycerin as a plasticizing agent, the production of blends with poly(caprolactone) (PCL), and finally the development of biocomposite materials reinforcing the blend of thermoplastic lignin and PCL with stone groundwood fibers (SGW). The results obtained show that thermoplastic lignin alone cannot be used as a bioplastic. However, its combination with PCL provided a tensile strength of, e.g., 5.24 MPa in the case of a 50 wt.% blend. In addition, when studying the properties of the composite materials, it was found that the tensile strength of a blend with 20 wt.% PCL increased from 1.7 to 11.2 MPa with 40 wt.% SGW. Finally, it was proven that through these biocomposites it is possible to obtain a correct fiber–blend interface. [ABSTRACT FROM AUTHOR]

Thermomechanical pulp (TMP) fibres can serve as renewable, cost-efficient and lightweight reinforcement for thermoplastic polymers such as poly(lactic acid) (PLA). The reinforcing ability of TMP fibres can be reduced due to various factors, e.g., insufficient dispersion of the fibres in the matrix material, fibre shortening under processing and poor surface interaction between fibres and matrix. A two-level factorial design was created and PLA together with TMP fibres and an industrial and recyclable side stream were processed in a twin-screw microcompounder accordingly. From the obtained biocomposites, dogbone specimens were injection-moulded. These specimens were tensile tested, and the compounding parameters statistically evaluated. Additionally, the analysis included the melt flow index (MFI), a dynamic mechanical analysis (DMA), scanning electron microscopy (SEM) and three-dimensional X-ray micro tomography (X- μ CT). The assessment provided insight into the microstructure that could affect the mechanical performance of the biocomposites. The temperature turned out to be the major influence factor on tensile strength and elongation, while no significant difference was quantified for the tensile modulus. A temperature of 180 °C, screw speed of 50 rpm and compounding time of 1 min turned out to be the optimal settings. [ABSTRACT FROM AUTHOR]

In engineering applications, natural fiber composites must comply with fire requirements including the use of flame retardant. Furthermore, biocomposites are known to be water sensitive. Whether flame retardants affect the water sensitivity and whether water absorption affects the fire behavior and the mechanical performance of biocomposites are the two main topics addressed in this work. In this study, a flax fiber/epoxy composite flame retardant with 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide (DOPO) or aluminum diethyl phosphinate (AlPi) was aged in humid atmosphere or by immersion in water. Water absorption kinetics revealed that DOPO induces an increase in equilibrium water content by approximately a factor of 2 due to its intrinsic hygroscopicity and/or its plasticizing effect on the epoxy matrix. In contrast, AlPi does not significantly change the water sensitivity of the biocomposite. Mechanical testing highlighted that, whatever the FR, the evolution of mechanical properties with ageing is governed by the moisture content. The drop of elastic modulus was attributed to a decrease in fiber rigidity due to plasticization, while the increase in tensile strength was assigned to an increase in fiber/matrix friction due to fiber swelling. As regards flame retardancy, only the highest water contents modified the fire behavior. For the AlPi containing biocomposite, the water release resulted in an increase by 50% of the time to ignition, while for the DOPO flame retardant biocomposite the water release was mainly postponed after ignition. [ABSTRACT FROM AUTHOR]

In the present investigation, the effects of fiber content (20, 30 and 40 wt%) and annealing heat treatment on the thermal properties of the biocomposite material formed by an isotactic polypropylene polymeric matrix (iPP) reinforced with short bamboo fibers (PP/BF) were studied. The coupling agent was iPP with grafting of maleic anhydride molecules (MAPP). The Differential Scanning Calorimetry (DSC) technique was used to determine the melting temperature (Tm), crystallization temperature (Tc), and degree of crystallinity (Xc) of the biocomposites. The melting temperature of pure PP was not significantly affected by the presence of bamboo fibers. However, the degree of crystallinity of PP increased with fiber content. The annealing heat treatment caused an increase in the Tm of pure PP and PP/BF. The composite with 20 wt% fiber content (PP/20F) annealed achieved the highest Xc (37,47 %). The Tc of polypropylene increased with the presence of fibers, and the PP/20F composite reached the highest value (115 °C). Also, the study of the Tm of the biocomposites in amorphous state was carried out, and it was observed that the sample with a fiber content of 30 wt% presented an endothermic peak at a temperature of approximately 168 °C. [ABSTRACT FROM AUTHOR]

To efficiently and economically utilize a wood-plastic biocomposite, an eco-friendly biocomposite was prepared using modified poplar fiber and polylactic acid (PLA) via 3D printing technology for the first time. First, the effects of poplar fiber (0, 1, 3, 5, 7, and 9%) on the mechanical and rheological properties of the printed biocomposites were investigated. Subsequently, the printing parameters, including printing temperature, speed, and layer thickness, were optimized to obtain the biocomposite with superior properties. Finally, four printing orientations were applied to the biocomposite based on the optimized printing parameters to study the effect of filament orientation on the properties of the biocomposite. Favorable printability and mechanical properties of the biocomposite were obtained at 5% poplar fiber. The optimal printing temperature of 220 °C, speed of 40 mm/s, and layer thickness of 0.2 mm were obtained to produce the desired mechanical properties of the biocomposite with the printing orientation in a longitudinal stripe. However, the printing parameters should be chosen according to the applications, where different physical and mechanical properties are needed to achieve efficient and economical utilization of the biocomposites. [ABSTRACT FROM AUTHOR]

Mechanical properties of Roselle fiber reinforced vinyl ester biocomposite were studied based on the fiber content and length in the present communication. Usually, natural fiber reinforced polymer composites depend on some aspects such as fiber content, fiber length and orientation, the fiber-matrix adhesion. Composite plates were prepared by a simple hand lay-up technique for two different fiber lengths (3 and 13 mm) and five different fiber content (10, 20, 30, 40 and 50 wt%). Composite specimens were tested according to ASTM and ISO standards and their results were recorded. Experimental results showed that mechanical properties such as tensile, flexural and impact, increases with increase of fiber content up to 40 wt% after which it is decreases at both the fiber length. However, modulus values were increased linearly with fiber content of 10 to 50 wt%. Composites with the fiber length of 13 mm show the high level of mechanical properties compared to composites with the fiber length of 3 mm at all combinations of fiber contents. It is observed that the optimal fiber content is 40 wt%, which can be used to obtain the maximum property level in the Roselle fiber reinforced vinyl ester composites. [ABSTRACT FROM AUTHOR]

New biocomposites are increasingly being developed and applied in engineering and manufacturing. The reinforcement type used in biocomposite is one of the major factors that greatly affect the machinability of biocomposite. This study investigated the drilling of two biocomposites (polypropylene-based biocomposite reinforced with biocarbon M1 (30 wt% biocarbon + PP/POE/MAPP) and chopped miscanthus fibers M2 (30 wt% miscanthus + PP/POE/MAPP)). A full factorial design was used for this study. The effects of drilling parameters and reinforcement types on surface roughness, thrust force, specific cutting energy, fine particles, and ultrafine particle generation were measured and analyzed. The results show that the thrust force and specific cutting energy during drilling of biocomposite M1 is bigger than that of biocomposite M2 under the same cutting conditions. However, the surface roughness and fine dust emitted when drilling biocomposite M1 are smaller than those from biocomposite M2, respectively. The reinforcement types of biocomposite, cutting parameters and drill diameter greatly affected fine particles emission. Meanwhile, the cutting conditions are not statistically significant for ultrafine particle generation during dry drilling of both biocomposites. [ABSTRACT FROM AUTHOR]

In the present investigation, the tensile mechanical properties of the isotactic polypropylene (PP) biocomposite material reinforced with randomly oriented short bamboo fiber bundles were determined. Samples of the material with different reinforcement contents (20, 30 and 40%) were prepared, using polypropylene with grafts of maleic anhydride molecules (MAPP) as coupling agent. A group of these samples were subjected to an accelerated thermal aging treatment to evaluate the effect of said treatment on the tensile properties of the biocomposite. Tensile tests were carried out at different deformation rates (10 and 50 mm/min) and an increase in tensile strength (29 to 45 MPa) and elastic modulus (1 to 3 GPa) of the PP with the fiber content was obtained. For different stretching speeds, better resistance at high speeds was obtained. Thermal aging for 24 hours at 100 °C increased the resistance of pure PP. For the biocomposites, a low resistance was obtained in the samples aged in greater time (98 °C, 10 days). Through scanning electron microscopy, a microstructural characterization was carried out that allowed explaining the improvement of the resistance of the fiber reinforced PP, and in some cases, the loss of resistance due to heat treatment. [ABSTRACT FROM AUTHOR]

In the material extrusion of the thermoplastic filaments, known as Fused Deposition Modelling, usually, pure thermoplastic polymers are used. Recently, the focus of the research is given to the development of new biocomposite thermoplastic materials. In our research, 3D printable biocomposite filaments, made with the addition of 50 wt.% of cardboard dust to the HDPE and PLA polymer matrix were studied. The influence of the added cardboard dust on structural, morphological and mechanical properties of the 3D printable biocomposite filaments was investigated. With the addition of the corrugated cardboard dust into the HDPE and PLA polymer matrix the changes in density, uniformity, chemical structure and transition temperatures of the samples were detected. The addition of the cardboard dust into the HDPE polymer matrix lead to low tenacity, toughness, deformability resulting in brittleness of the 3D printable biocomposite filament, whereas the addition of the cardboard dust into the PLA polymer matrix lowered tensile properties, but didn't affected bending toughness and has even improved compression strength of the 3D printable filament. [ABSTRACT FROM AUTHOR]

We analyzed the problematic textile fiber waste as potential precursor material to produce multilayer cotton fiber biocomposite. The properties of the products were better than the current dry bearing type particleboards and ordinary dry medium-density fiberboard in terms of the static bending strength (67.86 MPa), internal bonding strength (1.52 MPa) and water expansion rate (9.57%). The three-layer, four-layer and five-layer waste cotton fiber composite (WCFC) were tried in the experiment, the mechanical properties of the three-layer WCFC are insufficient, the five-layer WCFC is too thick and the four-layer WCFC had the best comprehensive performance. The cross-section morphology of the four-layer WCFC shows a dense structure with a high number of adhesives attached to the fiber. The hardness and stiffness of the four-layer cotton fiber composite enhanced by the high crystallinity of cellulose content, and several chemical bondings were presence in the composites. Minimum mass loss (30%) and thermal weight loss rate (0.70%/°C) was found for the four-layer WCFC. Overall, our findings suggested that the use of waste cotton fiber (WCF) to prepare biocomposite with desirable physical and chemical properties is feasible, and which can potentially be used as building material, furniture and automotive applications. • We study the potential use of waste cotton fiber in different-layer composites. • We used water, hot pressing and epoxy adhesives to fabricate the novel composite. • Cell wall collapses and chemical bonds enhanced the mechanical bonding. • It showed better mechanical properties compared to existing medium density boards. • Four-layer waste cotton fiber composite are the best preparation process. [ABSTRACT FROM AUTHOR]

Biodegradable fiber-reinforced biocomposites from steam-exploded coconut fibers and polylactic acid (PLA) and polybutylene succinate (PBS) plastic were developed in this study. Biocomposite filaments and samples were produced using a commercial-scale screw extruder and a 3D printer, respectively. In-depth mechanical and thermal analyses were also performed. The results showed that the tensile strengths of PLA mixed with 3% coconut fiber (PLA97/F3) and 6% coconut fiber (PLA94/F6) decreased by approximately 22% and 23%, respectively, compared to the 64% reduction of that of the original PLA after four-week storage. The bending modulus of the PLA/fiber composite was better than that of the original PLA (21–29% higher), whereas a 5–8% improvement was observed for the PLA/PBS/fiber composites. The impact strengths of PLA97/F3 and PLA77/PBS20/F3 were approximately 8.5% and 7.4% higher than those of the original PLA and PLA/PBS, respectively. During the degradation test, both PLA97/F3 and PLA77/PBS20/F3 exhibited higher tensile strengths than the original materials. Finally, this research presents encouraging results for the production of biodegradable fiber-reinforced biocomposites that are applicable to 3D printing platforms. The final products can be used as replacement or aftermarket components of automobiles. • PLA, PBS, and steam-exploded coconut fiber were used for filament production. • The 3D-printed biocomposites were subjected to mechanical and thermal tests. • Coconut fiber is effective as a natural fiber reinforcement material. • The products have higher tensile strengths than original materials during degradation test. [ABSTRACT FROM AUTHOR]

Consecutive superheated steam-alkali treatment was introduced to modify oil palm mesocarp fiber (OPMF) prior to biocomposite fabrication. The biocomposite made up of 70 wt.% modified OPMF (SNOPMF) and 30 wt.% poly(butylene succinate) (PBS) was prepared by melt blending followed by compression molding. A silane coupling agent of 3- aminopropyltrimethoxysilane (APTMS) was also incorporated into the SNOPMF/PBS biocomposite during the compounding process to impart better adhesion at the SNOPMF-PBS interface. The experimental results revealed that the tensile, flexural, and impact strengths were enhanced by 16, 30, and 15%, respectively, after the introduction of 2 wt.% APTMS to the SNOPMF/PBS biocomposite. Similarly, the resistance to water uptake and thickness swelling of this biocomposite was improved by 34 and 49%, respectively, relative to SNOPMF/PBS biocomposite. The SEM observation of the tensile fracture surface showed that APTMS improved the interfacial adhesion between SNOPMF and PBS. Based on the results, it can be deduced that APTMS could be a good coupling agent for improving the SNOPMF-PBS adhesion and, thereby, lead to a water resistant biocomposite of enhanced mechanical properties. [ABSTRACT FROM AUTHOR]

A new class of biocomposites based on oil palm empty fruit bunch fiber and poly(butylene adipate-co-terephthalate) (PBAT), which is a biodegradable aliphatic aromatic co-polyester, were prepared using melt blending technique. The composites were prepared at various fiber contents of 10, 20, 30, 40 and 50 wt% and characterized. Chemical treatment of oil palm empty fruit bunch (EFB) fiber was successfully done by grafting succinic anhydride (SAH) onto the EFB fiber surface, and the modified fibers were obtained in two levels of grafting (low and high weight percentage gain, WPG) after 5 and 6 h of grafting. The FTIR characterization showed evidence of successful fiber esterification. The results showed that 40 wt% of fiber loading improved the tensile properties of the biocomposite. The effects of EFB fiber chemical treatments and various organic initiators content on mechanical and thermal properties and water absorption of PBAT/EFB 60/40 wt% biocomposites were also examined. The SAH-g-EFB fiber at low WPG in presence of 1 wt% of dicumyl peroxide (DCP) initiator was found to significantly enhance the tensile and flexural properties as well as water resistance of biocomposite (up to 24%) compared with those of untreated fiber reinforced composites. The thermal behavior of the composites was evaluated from thermogravimetric analysis (TGA)/differential thermogravimetric (DTG) thermograms. It was observed that, the chemical treatment has marginally improved the biocomposites' thermal stability in presence of 1 wt% of dicumyl peroxide at the low WPG level of grafting. The improved fiber-matrix surface enhancement in the chemically treated biocomposite was confirmed by SEM analysis of the tensile fractured specimens. [ABSTRACT FROM AUTHOR]

Low-porosity materials based on hot-pressed wood fibers or nanocellulose fibrils (no polymer matrix) represent a new concept for eco-friendly materials with interesting mechanical properties. For the replacement of fossil-based materials, physical properties of wood fiber materials need to be improved. In addition, the carbon footprint and cumulative energy required to produce the material also needs to be reduced compared with fossil-based composites, e.g., glass fiber composites. Lignin-containing fibers and nanofibers are of high yield and special interest for development of more sustainable materials technologies. The present mini-review provides a short analysis of the potential. Different extraction routes of lignin-containing wood fibers are discussed, different processing methods, and the properties of resulting fiber materials. Comparisons are made with analogous lignin-containing nanofiber materials, where mechanical properties and eco-indicators are emphasized. Higher lignin content may promote eco-friendly attributes and improve interfiber or interfibril bonding in fiber materials, for improved mechanical performance. [ABSTRACT FROM AUTHOR]

Biotechnological use of probiotic microorganisms involves providing them with appropriate conditions for growth, but also protection against environmental changes caused by an exchange of the medium, isolation of metabolites, etc. Therefore, the research on effective immobilization of probiotic microorganisms should be focused in this direction. The present study aimed to evaluate the effectiveness of an innovative hybrid immobilization system based on electrospun nanofibers and alginate hydrogel. The analyses carried out included the study of properties of the initial components, the evaluation of the degree and durability of cell immobilization in the final material, and their survival under stress conditions. Effective binding of microorganisms to the hydrogel and nanofibers was confirmed, and the collected results proved that the proposed biocomposite is an efficient method of cell protection. In addition, it was shown that immobilization on electrospun nanofibers leads to the preservation of the highest cell activity and the least cell growth restriction as compared to free or lyophilized cells only. The completed research opens new perspectives for the effective immobilization of microorganisms of significant economic importance. [ABSTRACT FROM AUTHOR]

Bio- and green composites are mainly used in non-structural automotive elements like interior panels and vehicle underpanels. Currently, the use of biocomposites as a worthy alternative to glass fibre-reinforced plastics (GFRPs) in structural applications still needs to be fully evaluated. In the current study, the development of a suited biocomposites started with a thorough review of the available raw materials, including both reinforcement fibres and matrix materials. Based on its specific properties, hemp appeared to be a very suitable fibre. A similar analysis was conducted for the commercially available biobased matrix materials. Greenpoxy 55 (with a biocontent of 55%) and Super Sap 100 (with a biocontent of 37%) were selected and compared with a standard epoxy resin. Tensile and three-point bending tests were conducted to characterise the hemp-based biocomposite. [ABSTRACT FROM AUTHOR]

Herein, we used intense shear to construct caterpillar-like continuous hierarchical fibers (CLCHF). This architecture was then modified with mussel inspired poly(dopamine) (PDA) and γ-methacryloxypropyl trimethoxy silane (KH570) in a one-step method. Finally, employing (PDA + KH570)@CLCHF and compounded with poly(butylene succinate) (PBS) ultrafine fiber, (PDA + KH570)@CLCHF/PBS biocomposite was manufactured by combining intense shear and thermal-compression method. In virtue of intense shear, CLCHF can be effectively produced with nanoscale fibrils from 2 nm to 28 nm and (PDA + KH570)@CLCHF and PBS ultrafine fibers displayed favorable homogenization in aqueous solution. More importantly, the interspace between (PDA + KH570)@CLCHF and PBS ultrafine fibers could be optimized to facilitate infiltration at high filler content in polymers. The results also showed that the PBS biocomposite with 30 wt% (PDA + KH570)@CLCHF displayed optimal mechanical performance. Its tensile strength, elastic modulus, flexural strength, flexural modulus and impact strength reached to 120.2 MPa, 6.4 GPa, 110.1 MPa, 4.0 GPa and 23.5 kJ/m2, respectively. It is noticeble that the tensile properties were superior to some previously reported PBS biocompoistes due to the ability of CLCHF to effectively hinder the aggregation of numerous microcracks and slow crack tip propagation. The (PDA + KH570)@CLCHF/PBS biocomposites reported here can be used as desirable substitutes for nondegradable composites due to its high value added and favorable mechanical performance, and may broaden the application prospect of PBS biocomposite. [ABSTRACT FROM AUTHOR]

In this study, the application of hydrocolloid and fiber industry wastes and their transformation in biochar and biocomposite as biosorbents for emerging pollutants effective removal was carried out. Initially, the adsorption ability of six different wastes was ascertained in single and competitive removal of sulfamethoxazole (SMX) and methylparaben (MePa). Among them, fiber extraction process wastes presented the best result attaining maximum uptakes with removal levels up to 23 and 48% of MePa and SMX, respectively. The adsorption capacity was enhanced by fiber waste biochar preparation at 500 °C and 30 min under nitrogen atmosphere, and improved by the preparation of laccase-biocomposites, achieving maximum uptakes more than ten-fold the obtained using raw material. The simultaneous removal of the pollutants by the biocomposite followed a pseudo-second order kinetic and resulted in maximum uptakes of 24.06 and 23.15 mg/g for SMX and MePa, respectively. Finally, raw material and laccase-biocomposite behaviours were simulated by homogeneous surface diffusion model. Previously, the isotherms were studied fitting well to Freundlich model. The obtained results remarked the feasibility of laccase-biocomposite in which reactive groups incorporation on the biochar surface could be responsible for facilitating the pollutants removal from the aquatic environment. Image 1 • Lime and lemon waste (LL) could be used as biosorbent at low PPCPs concentration. • SMX and MePa sorption intensity of LL was enhanced by biochar preparation (Bc). • Biocomposite made by laccase adsorption on Bc (BcL) modified its surface increasing the uptake. • BcL improved the uptake values more than 10-fold the maximum level of LL. • Upscaling fixed bed adsorption column was modelled using LL and BcL in flow system. [ABSTRACT FROM AUTHOR]

Composites containing bio-based materials, like banana fiber and poly(lactic acid) (PLA), are potential food-packaging materials. We carried out an environmental life cycle assessment (LCA) of coffee jar lids made from high density polyethylene (HDPE), PLA, and banana fiber to assess their environmental performance. We considered differences in the type of blend (content of PLA and banana fiber in the composite), origin of the banana fiber feedstock (considered as either biowaste or as a co-product from banana production) and banana fiber pretreatment conditions (either no pretreatment or pretreatment using chemicals). Irrespective of the scenario, a lid made from 40% banana fiber and equal amounts of HDPE and PLA performed significantly better in all 18 impact categories when compared to a lid made from 100% PLA. By contrast, the same lid performed significantly better in 3 impact categories only (climate change, photochemical oxidant formation and fossil depletion) when compared to a lid made from 100% HDPE. Thus, environmental performance of the biocomposite strongly depends on which polymer base is replaced by the banana fiber in the composite. Replacing PLA with banana fiber is generally expected to bring environmental benefits. Image 1 • Environmental performance of new biocomposite lids strongly depends on polymer base. • 40% banana fiber lid performs environmentally better than poly(lactic acid) one. • 40% banana fiber lid performs better in 3 impact than high density polyethylene lid. [ABSTRACT FROM AUTHOR]

In this study, a mixture of thermoplastic polybutylene succinate (PBS), tapioca starch, glycerol and empty fruit bunch fiber was prepared by a melt compounding method using an industrial extruder. Generally, insertion of starch/glycerol has provided better strength performance, but worse thermal and water uptake to all specimens. The effect of fiber loading on mechanical, morphological, thermal and physical properties was studied in focus. Low interfacial bonding between fiber and matrix revealed a poor mechanical performance. However, higher fiber loadings have improved the strength values. This is because fibers regulate good load transfer mechanisms, as confirmed from SEM micrographs. Tensile and flexural strengths have increased 6.0% and 12.2%, respectively, for 20 wt% empty fruit bunch (EFB) fiber reinforcements. There was a slightly higher mass loss for early stage thermal decomposition, whereas regardless of EFB contents, insignificant changes on decomposition temperature were recorded. A higher lignin constituent in the composite (for high natural fiber volume) resulted in a higher mass residue, which would turn into char at high temperature. This observation indirectly proves the dimensional integrity of the composite. However, as expected, with higher EFB fiber contents in the composite, higher values in both the moisture uptake and moisture loss analyses were found. The hydroxyl groups in the EFB absorbed water moisture through formation of hydrogen bonding. [ABSTRACT FROM AUTHOR]

Recycled polylactic acid (PLAr) was reinforced with treated nanocellulosic hemp fibers for biocomposite fabrication. Cellulosic fibers were extracted from hemp fibers chemically and treated enzymatically. Treated nanocellulosic fibers (NCF) were analyzed by Fourier-transform infrared spectroscopy, X-ray diffraction, and scanning electron microscopy. Biocomposite fabrication was done with PLAr and three concentrations of treated NCF (0.1%, 0.25%, and 1% (v/v)) and then studied for thermal stability and mechanical properties. Increased thermal stability was observed with increasing NCF concentrations. The highest value for Young's modulus was for PLAr + 0.25% (v/v) NCF (250.28 ± 5.47 MPa), which was significantly increased compared to PLAr (p = 0.022). There was a significant decrease in the tensile stress at break point for PLAr + 0.25% (v/v) NCF and PLAr + 1% (v/v) NCF as compared to control (p = 0.006 and 0.002, respectively). No significant difference was observed between treatments for tensile stress at yield. [ABSTRACT FROM AUTHOR]