Characterization of novel natural cellulose fiber from Ficus macrocarpa bark for lightweight structural composite application and its effect on chemical treatment.

This study investigates Ficus Macrocarpa tree bark fibers (FMB) as a sustainable alternative reinforcement for polymer composites. The Industrial Revolution marked the evolution of polymer composites with synthetic material reinforcement, leading to environmental concerns. Natural fibers have recently gained prominence as efficient alternatives for polymer composites. Despite numerous natural fibers being considered, ensuring a sustainable raw material source remains crucial. In this study, fibers were extracted from FMB and subjected to alkali treatment to evaluate their impact on physical, chemical, and thermal properties. Initially, the extracted fibers measured 253.80 ± 15 µm in diameter, reduced to 223.27 ± 12 µm post-alkali treatment. Chemical analysis showed an increase in cellulose content to 59.7 wt%, a 23.34 % improvement over untreated fibers (48.4 wt%). The crystalline index for untreated and treated fibers measured 80.20 % and 84.75 %, respectively, with no noticeable changes in the cellulose phase. Additionally, the crystalline size increased to 3.21 nm. Thermogravimetric analysis demonstrated enhanced stability of treated fibers up to 378.87 °C, while the kinetic activation energy remained constant at 64.76 kJ/mol for both the treated and the untreated fibers. The alkali treatment further improved surface roughness to 39.26, confirmed by scanning electron microscopic images. These findings highlight the potential of cellulose fibers from Ficus Macrocarpa bark as a sustainable and environmentally friendly replacement for synthetic fibers in polymer composites. The enhanced physical properties and excellent thermal stability make them a promising choice for eco-conscious materials.

Pedalium murex plant-based bioplasticizer reinforced polylactic acid films: A promising approach for biodegradable fruit packaging applications.

The most likely materials for use in packaging are plastics. A lot of synthetic polymers are harming the environment. A plasticizer is required for all polymers to improve their characteristics and workability. The plasticizers come in liquid form and are also derived from fossil fuels, which are harmful to the environment. Producing functional and affordable biopolymer for packaging applications is a difficult task nowadays. The preparation of biofilm for packaging using biopolymer and bioplasticizer is the main aim of this work. The biopolymer poly L-lactic acid (PLA) is used, and the bio plasticizer is extracted from Pedalium murex plant. Chemical and mechanical methods are used to extract the plasticizer. Plasticization of polylactic acid biopolymer was done using the extracted plasticizer at additions of 1 %, 2 %, 3 %, 4 %, and 5 %. FT-IR spectroscopy, X-ray diffraction spectroscopy, and surface roughness values are used to characterise the prepared biofilms. Scanning electron spectroscopy pictures are utilised to evaluate the morphological orientation of the biofilms. Strawberries packed with biofilms are used to evaluate the barrier properties of biofilms using UV spectroscopy analysis. Thermal degradation behaviour is investigated using thermo gravimetric analysis. We examined the mechanical characteristics, such as tensile strength, elongation modulus, and elongation break percentage. The plasticizing effect of the plasticizer raises the elongation break percentage while decreasing the tensile strength and modulus. For 2 % plasticizer addition the elongation break increases and the tensile not much affected. To demonstrate biodegradability and microbial resistance, the soil degradation behaviour and antimicrobial activities were examined.

Era of bast fibers-based polymer composites for replacement of man-made fibers.

Bast fibers are defined as those obtained from the outer cell layers of the bast of various plant families. They are finding use in textile applications and are widely used as reinforcements for green composites, as bast fibers are perceived as "sustainable". There is a growing demand for bast fibers across the world due to their renewable and biodegradable nature. The bast fibers are mainly composed of cellulose, which potentially considers the growing techniques, harvesting and extraction processes of bast fibers most used to produce fibers with appropriate quality to apply in the daily lives of modern men and women in contemporary society. This review paper looks at many aspects of natural fibers, with a focus on plant bast fibers, including their impact on prehistoric and historical society. This review shows that bast fibers are competitive compared to man-made fibers in many applications, but variability in mechanical properties and low tenacity may limit their use in high-strengthh composites and extend to, particularly in aerospace, automotive, packaging, building industries, insulation, E-composites (Eco composites), geotextiles and many other applications are currently being explored. Considering, important characteristics of bast fibers include physical, mechanical, and chemical properties. This makes bast fibers one of the most important classes of plant fibers to use as reinforcing agents in thermosetting/thermoplastic polymer matrices. And the effect of bast fibers as reinforcement in the properties of ECO-composites, GREEN-composites, BIO-composites, lightweight composites. Bast fibers play an important role in sustainability, the preservation of the health of the environment, the well-being of the next generation, and even the daily lives of men and women in the contemporary world.

Isolation and characterization of novel bioplasticizers from rose (Rosa damascena Mill.) petals and its suitability investigation for poly (butylene adipate-co-terephthalate) biofilm applications.

The current growing environmental awareness has forced the use of biodegradable plasticizers, which are sustainable and abundant in plant resources. Rose petal plasticizers (RPP) act as an actual substitute for chemical plasticizers in this situation as they are biocompatible and biodegradable. Chemical procedures like amination, alkalization, and surface catalysis are used to extract the natural emollients from rose petals. XRD, FT-IR, and UV studies were used to understand the characteristics of the rose petal plasticizer. Based on the XRD data, the RPP's crystallinity size (CS) and crystallinity index (CI) values were determined to be 9.36 nm and 23.87%, respectively. The surface morphology of the isolated plasticizer is investigated using SEM, EDAX analysis and AFM. RPP surface pores with rough surfaces are visible in SEM images, which make them appropriate for plasticizing novel bioplastics with superior mechanical qualities. The plasticizer's heat degradation behaviour is investigated using thermogravimetric and differential thermogram analysis curves. Following the characterization of the synthesised molecules, the plasticization effect was examined using a biodegradable polymer matrix called poly (butylene adipate-co-terephthalate) (PBAT). The reinforcement interface was also examined using scanning electron microscopy analysis. RPP-reinforced films demonstrated greater flexibility and superior surface compatibility at a 5% loading compared to PBAT-only films. Based on a number of reported features, RPP could be a great plasticizer to address future environmental problems.

Effect of chemical treatment on physio-mechanical properties of lignocellulose natural fiber extracted from the bark of careya arborea tree.

For the first time, the current work has carried out a chemical treatment of a novel ligno-cellulose fiber that is extracted from the bark of an unexplored plant of Careya arborea. Careya arborea (CA), a flowering tree known for its green berries, thrives in the Indian subcontinent and Afghanistan. This research was focused on extracting fibers from the bark of the Cary tree for the first time to corroborate the influence of chemical treatment on its different characteristics. These CA fibers have a high proportion of cellulose, consisting of 71.17 wt percent, together with 27.86 wt percent of hemicellulose, and a reduced density of 1140 kg/m3, making them a suitable candidate for creating lightweight applications in a variety of industries. Chemical treatment has done on the cay fiber with the concentrations of NaOH 5 (wt%), 10 (wt%), and 15 (wt%) solution mixture to improve their characteristics. Estimated the difference between Chemically processed and non-processed Cary fibers and corroborated in results. We performed a number of experiments, including FTIR, XRD, SEM, EDAX, AFM, and TGA, to fully comprehend the changing properties. Chemical testing showed that cellulose changed from its non-crystalline state to cellulose, proving that the treatment was successful in changing the fibre structure. Additionally, the thermo-gravimetric examination showed higher thermal stability 248 °C-325 °C and a rise in the crystallinity index, indicating the treated fibers' improved potential for high-temperature applications. The treated Cary fibers exhibited excellent surface properties, promising improved adhesion, mechanical performance, offering lightweight and sustainable solutions for diverse applications.

Waste chicken feather biofiller reinforced bioepoxy resin based biocomposites - A waste to wealth experimental approach.

Utilizing poultry wastes, particularly chicken feathers, in biopolymer composites is seen as an important aspect in lowering the environmental pollution and paving a new path to sustainability. The main objective of this experimental study is to develop polymer composites reinforced with waste chicken feather fillers and evaluate their physical, mechanical, and thermal characteristics. The composites were fabricated through an open mold casting process using bio epoxy (SR-33 Greenpoxy) as the matrix and chicken feather filler as a reinforcement in three distinct weight fractions (2.5, 5, and 7.5 wt%). To evaluate the effects of filler content on the mechanical properties of the fabricated bio-epoxy composites, they were subjected to tensile, flexural, impact, and hardness tests. The findings from the experimental studies demonstrated that the composites containing 2.5 wt% of chicken feather filler had improved mechanical properties, thermal stability, and crystallization behaviour. The thermal attributes of samples included a greater melting point, lower recrystallization temperature, higher glass transition temperature, and quicker crystallization rates. The Scanning Electron Microscope analysis of the fracture surface morphology of the biocomposites showed a better interfacial adhesion between the filler and matrix. It could be concluded from the results that the waste chicken feather can be used as potential filler reinforcements for begetting natural composites for various low- and medium-density structural and non-structural applications.

Characterization of new cellulose fiber extracted from second generation Bitter Albizia tree.

The present work examines the physical, thermal tensile, and chemical properties of wood skin fibers obtained from second generation Bitter Albizia (BA) tree skin. Chemical characterization of BA fibers showed the presence of various chemical contents such as cellulose of 74.89 wt. %, hemicellulose of 14.50 wt. %, wax of 0.31 wt. %, lignin of 12.8 wt. %, moisture of 11.71 wt. %, and ash of 19.29 wt. %. The density of BA fibers (BAFs) was showed 1285 kg/m3. XRD analysis of BAFs showed a crystallinity index (CI) of 57.20% and size of crystallite of 1.68 nm. Tensile strength and strain to failure of BAFs examined through tensile test were 513-1226 MPa and 0.8-1.37% respectively. TGA portrayed the thermal steadiness of BAFs as 339 °C with 55.295 kJ/mol kinetic activation energy, its residual mass was 23.35% at 548 °C. BAFs with high CI, less wax content, and better tensile strength make more suitable for making polymer matrix composites. SEM images of the BAFs surface depicted that the fiber outer surface has more rough which shows that they can contribute to hige fiber-matrix adhesion during composites preparation.

Facile exfoliation and physicochemical characterization of Thespesia populnea plant leaves based bioplasticizer macromolecules reinforced with polylactic acid biofilms for packaging applications.

Plasticizers are active ingredients added to the polymer to increase its workability. Since synthetic plasticizer is not ecofriendly and toxic in nature, it is a real cause for concern. On this basis, our study focuses on plasticizer extraction from plant-based resources. In this research work, Thespesia populnea leaves are utilized for the isolation of biological macromolecules with a plasticizing effect for biofilm applications. This extraction process is done through solvent extraction, amination, slow pyrolysis, and surface catalysis process. The physico-chemical and microstructural characterization of novel plasticizer particles were studied for the first time. The lower crystallinity index and crystalline size obtained from X-ray diffraction is 50.08 % and 20.45 nm respectively. Energy dispersive spectroscopy, particle sizer analysis, atomic force microscopy, and scanning electron microscopy are used to assess surface morphology of this plasticizer. The thermogram and differential thermal analysis curves give the information about degradation behavior of plasticizers and their thermal stability. The glass transition temperature of the extracted plasticizer is 60.56 °C. The plasticizing effect of the plasticizer is studied through film fabrication of polylactic acid which was blended with the extracted plasticizer. The mechanical property of biofilm was improved with the addition of plasticizer. The elongation break percentage (for 5 % plasticizer 46.12 %) was increased compared to others with moderate tensile strength. However, the tensile and elongation modulus decreases with the increase of plasticizer content. The crystallinity of the PLA film was improved after the plasticization. The thermal stability also increased with 3 % addition of the plasticizer. The isolated plasticizer was soluble in water and its molecular weight ≈380.

Extraction of nano-crystalline cellulose for development of aerogel: Structural, morphological and antibacterial analysis.

In the present decades, nanocellulose has been very popular in the field of nanotechnology and is receiving much attention from researchers because of its advantageous physicochemical properties, high aspect ratio, and high specific strength and modulus. The available non-eco-friendly conventional methods for the extraction of nano-crystalline cellulose (NCC) use highly concentrated chemicals and are time-consuming as well. The present adopted cost-effective method for the extraction of nano-crystalline cellulose involves minimum usage of chemicals and is environmentally friendly and relatively fast compared to other conventional methods. The nano-crystalline cellulose from sisal (NCC-S) fibers were extracted by steam explosion-assisted mild concentrated chemical treatments followed by mechanical grinding. The Dynamic light scattering (DLS) and Transmission electron microscopy (TEM) characterization confirmed the size of extracted NCC-S. A high aspect ratio was observed as 19.23, which signifies it could be a promising reinforcing material in developing nanocomposites for advanced applications. An increase in crystallinity and the removal of amorphous materials for NCC-S were confirmed by X-ray diffraction (XRD) and Fourier-transform infrared spectroscopy (FTIR) analysis, respectively. Antibacterial study shows that NCC-S did not show any antibacterial properties against E. coli and S. aureus. The calculated yield of extracted nanocellulose was about 50 %. The aerogel with a porosity of 95.1 % and a density of 0.075 g/cm3 was prepared by vacuum freeze-drying method using extracted nanocellulose and chitosan. The cross-linking network structure and thermal stability of the aerogel were also confirmed by FTIR and TGA analysis respectively.

Lignocellulose based biofiller reinforced biopolymer composites from fruit peel wastes as natural pigment.

In this study, the utilization of mangosteen and durian peel wastes as bio-filler and natural pigment in biopolymer of polybutyrate adipate terephthalate (PBAT) were examined. The related research work of hybridization of both mangosteen and durian peels reinforced in biopolymer as cellulose-based bio fillers and natural pigment is rarely studied. The content variation of mangosteen powder and durian powder ranged from 0 to 30 wt% with an increment of 10. The influence of mangosteen and durian powders reinforced in PBAT on color change, morphological, chemical composition, mechanical, thermal, and rheological properties were determined. Mangosteen peel and durian peel provided dark appearance for the green composites without pre-burn of these fruit peels. It can be concluded that mangosteen peel and durian peel can be used as bio pigment and natural reinforcement material in biopolymer matrix which can reduce massive waste of mangosteen and durian peel and add value to these wastes. These black biopolymer composites can be used in applications of eco-friendly food packaging and medicine zipper packaging. The overall mechanical properties, thermal stability, and dark color of mangosteen/PBAT composites were greater than those of durian/PBAT composites. However, durian/PBAT composites presented greater thermal and rheological properties than mangosteen/PBAT composites.

Isolation and characterization of microcrystalline cellulose from an agro-waste tamarind (Tamarindus indica) seeds and its suitability investigation for biofilm formulation.

The exploration of potential bio-fillers for bio-film application is a promising approach to ensure biodegradable, eco-friendly, good-quality materials with high-performance applications. This is a comprehensive study executed to establish the utility of an agro-waste Tamarindus indica seeds for microcrystalline cellulose production and to assess its feasibility for biofilm fabrication. The extraction was carried out through consecutive chemical-mediated alkalization, acid hydrolysis and bleaching. The isolated microcrystalline cellulose from Tamarindus indica seeds (TSMCC) was characterized through chemical, thermal and morphological characterization to validate the cellulose contribution, thermal resistance, and compatibility of the material. The physical parameters as density and yield percentage were assessed to evaluate its light-weight utility and economic productivity. These examinations revealed that TSMCC has good specific properties such as high cellulose content (90.57 %), average density (1.561 g/cm3), feasible average roughness (12.161 nm), desired particle size (60.40 ± 21.10 µm), good crystallinity (CI-77.6 %) and thermal stability (up to 230 °C); which are worthwhile to consider TSMCC for bio-film formulation. Subsequently, bio-films were formulated by reinforcing TSMCC in polylactic acid (PLA) matrix and the mechanical properties of the bio-films were then studied to establish the efficacy of TSMCC. It is revealed that the properties of pure PLA film increased after being incorporated with TSMCC, where 5 %TSMCC addition showed greater impact on crystalline index (26.16 % to 39.62 %), thermal stability (333oc to 389 °C), tensile strength (36.11 ± 2.90 MPa to 40.22 ± 3.22 MPa) and modulus (2.62 ± 0.55GPa to 4.15 ± 0.53GPa). In light of all promising features, 5 % TSMCC is recommended as a potential filler reinforcement for the groundwork of good quality bio-films for active packaging applications in future.

Exfoliation and physico-chemical characterization of novel bioplasticizers from Nelumbo nucifera leaf for biofilm application.

Due to the extreme threats as environmental and health issues caused by the petroleum-based leachable plasticizers, researchers among different domains are more interested in finding unique biodegradable plasticizers from natural sources. The present study used Nelumbo nucifera leaf to extract novel biopolymers as viable substitutes for chemical plasticizers. The biopolymers extraction was carried out through chemical means and its physico-chemical and morphological characterization were carried out to confirm its plastic nature. The polymers extracted possess a low glass transition temperature (77.17 °C), good thermal stability (230 °C), low density (0.94 g/cc), good surface roughness (34.154 µm), low crystallinity index (25.1%) and moderate crystallite size (16.36 nm). The presence of an organic polymer with specific chemical groups as olefinic alkenes, epoxide, imino/azo groups, and hydrophobic organic siloxane groups, signify that the material is a condensed phenolic derivative. Furthermore, bio-film was formulated using NLP and poly lactic acid (PLA) matrix to evaluate its plasticizing effect and film-forming ability. Variation in specific properties of film was noted after bio-plasticizer addition, where tensile strength (20.94 ± 1.5 MPa to 19.22 ± 1.3 MPa) and Young's modulus (1.462 ± 0.43 GPa to 1.025 ± 0.52 GPa) was found to be decreased whereas increased the percentage of elongation at break (26.30 ± 1.1% to 39.64 ± 1.6%). In addition, decreased glass transition temperature (Tg) (59.17 °C), good surface compatibility, and increased flexibility of NLP-PLA film in contrast to pure PLA film authorizes the plasticizing effect of bio-plasticizers on PLA. Since the extracted bio-plasticizers could be a suitable replacement to harmful synthetic plasticizers for lightweight packaging applications in bioplastics sector.

Thermal, morphology and bacterial analysis of pH-responsive sodium carboxyl methylcellulose/ fumaric acid/ acrylamide nanocomposite hydrogels: Synthesis and characterization.

In this present investigation, sodium carboxymethyl cellulose grafted with Fumaric acid/Acrylamide (CMC/FA/AAm=CFA) hydrogel and their silver nanocomposite hydrogels (CFA-Ag x, x = 5, 10 and 20) were developed by simple, cost effective and ecofriendly greener method. Mint leaf extract was used as an efficient natural reducing agent due to presence of active and antioxidant potential of polyphenol and flavonoid components. Swelling equilibrium of CFA hydrogel showed Seq% 3000 both in pH medium and distilled water. CFA (90:10) hydrogel has been produced greater than Seq% 6000. The synthesized CFA (90:10)-Ag-5, CFA (90:10)-Ag-10 and CFA (90:10)-Ag-20 nanocomposite hydrogels have been observed lower Seq% 2000-3000 than the CFA hydrogel. The homogeneous distribution of AgNPs throughout the CFA hydrogel and nanocomposites has been explored by SEM analysis. The interaction of network heteroatoms with AgNPs has been strongly revealed by the FTIR spectra and XRD analysis. The thermal stability of CFA (90:10)-Ag-5, 10, and 20 nanocomposite hydrogels have showed greater stability than CFA hydrogel which is confirmed by TGA/DSC thermogram analysis. The TEM analysis was used to explore a uniform distribution of spherical AgNPs (10 nm-50 nm) embedded on the CFA composite hydrogel. The CFA (90:10)-Ag-20 nanocomposite hydrogel has showed good antibacterial activity beside E. coli (Gram positive) and S. aureus (Gram negative) pathogens. Based on the antibacterial activity and swelling properties of CFA-Ag nanocomposite hydrogels have the ability to accelerate the antibacterial activity and are potential candidates for medical and environmental applications.

Multi-analytical investigation of the physical, chemical, morphological, tensile, and structural properties of Indian mulberry (Morinda tinctoria) bark fibers.

In this study, micro-cellulosic fibers were isolated from the bark of Morinda tinctoria (MT) and characterized for the first time. The anatomical, physical, chemical, thermal, and mechanical properties of the M. tinctoria bark fiber (MTBF) were investigated. The mean diameter and density values were determined to be 32.013 ± 1.43 µm and 1.4875 g/cm³, respectively. Zeta potential analysis and particle size measurements provided the evidence of enhanced micro-particle behavior on the fiber's surface. Various structural characterizations confirmed the presence of polysaccharide structures, monosaccharide compositions, glycosidic residues (sugar linkages), and cohesive reactions of TMSA (Trimethylsilyl alditol) derivatives, indicating the fiber's potential for strong surface absorption properties. X-ray diffraction analysis revealed a crystallinity index of 51 % and a crystallite size of 3.086 nm for MTBF. Fourier transform infrared analysis indicated the presence of cellulose, hemicellulose, and lignin constituents, along with their corresponding functional groups. The calculated values of Young's modulus and tensile strength were determined to be 75.7 GPa and 746.77 MPa, respectively. Thermogravimetric analysis demonstrated the thermal stability of the extracted MTBF up to 240 °C. Based on these findings, the MT microfibrils derived from the bark can be considered as potential substitutes for existing synthetic composites, offering reinforcement for novel bio composites.

Assessment of biodegradation of lignocellulosic fiber-based composites - A systematic review.

Lignocellulosic fiber-reinforced polymer composites are the most extensively used modern-day materials with low density and better specific strength specifically developed to render better physical, mechanical, and thermal properties. Synthetic fiber-reinforced composites face some serious issues like low biodegradability, non-environmentally friendly, and low disposability. Lignocellulosic or natural fiber-reinforced composites, which are developed from various plant-based fibers and animal-based fibers are considered potential substitutes for synthetic fiber composites because they are characterized by lightweight, better biodegradability, and are available at low cost. It is very much essential to study end-of-life (EoL) conditions like biodegradability for the biocomposites which occur commonly after their service life. During biodegradation, the physicochemical arrangement of the natural fibers, the environmental conditions, and the microbial populations, to which the natural fiber composites are exposed, play the most influential factors. The current review focuses on a comprehensive discussion of the standards and assessment methods of biodegradation in aerobic and anaerobic conditions on a laboratory scale. This review is expected to serve the materialists and technologists who work on the EoL behaviour of various materials, particularly in natural fiber-reinforced polymer composites to apply these standards and test methods to various classes of biocomposites for developing sustainable materials.

Statistical approach on the inter-yarn friction behavior of the dual-phase STF/ρ-Aramid impregnated fabrics via factorial design and 3D-RSM.

Shear thickening fluids (STFs) refer to non-Newtonian fluids of the dilatant variety, wherein their viscosity experiences a significant surge with an escalation in the shear rate. In this investigative work, the friction behavior between yarns (pull-out) and absorption of static and kinetic energy during the phenomenon of friction between yarns in STFs are performed by monophase (MP-STF) adding nano SiO2 and dual-phase (MP-STF) adding carbon nanotubes. The ρ-Aramid fabrics were reinforced via the "foulard process", and carried out on MP-STF, and DP-STF/ρ-Aramid-impregnated fabrics to evaluate and compare with the enhancement in interfacial friction properties between yarns. The results showed that DP-STF has more significant than MP-STF and MP-STF in ultimate load, kinetic shear stress, static shear stress, and friction energy level effects. The DP-STF exhibits various friction enhancement mechanisms at the yarn interface, leading to higher absorption of static and kinetic energy related to interfacial friction, as indicated by the results obtained. Furthermore, the DP-STF/ρ-Aramid impregnated fabrics exhibited ultimate load (22.23 ± 0.522 N), kinetic shear stress (35.73 ± 0.850 MPa*100), static shear stress (36.28 ± 0.900 MPa*100), and friction energy level (610.33 ± 0.250). Increased ultimate load (581.7% and 180.7%), kinetic shear stress (621.4% and 174.6%), static shear stress (550.5% and 159.1%), and friction energy level (680.2 and 186.7%) compared to WT-STF and MP-STF, respectively. The current discoveries hold immense potential for various applications in the fields of engineering and smart material technologies. These applications span a multiplicity of industries, including sports products, medical advancements, space technology, as well as protective and shielding products.

Impact of yarn compositions, loop length, and float stitches on the mechanical behavior of knitted fabrics via full factorial design and RSM.

This article presents a study on the tensile properties of knitted fabrics commonly employed in polymeric matrix textile composites. The key mechanical parameters investigated include stress (Pa), strain, Young's modulus (Pa), and work of rupture (J). The knitted fabrics were developed using the Cixing Knitting System software and subsequently manufactured using a double jersey (electronic) flat knitting machine. The primary objective of this research was to explore the impact of various factors on the mechanical behavior of these knitted fabrics. The factors studied were wale and course directions, float stitch density, loop length (cm), and the type of synthetic knitting yarns used (100% polyester and 100% polyamide) along with different combinations of knitting yarns (100% cotton and 67% polyester/33% cotton hybrid). The adopted ASTM D 5034 standard, Response Surface Methodology (RSM), and Analysis of Variance (ANOVA) were employed to evaluate the mechanical performance of these fabric structures. The findings of the study revealed that the statistical adjustment of the data set for stress, strain, Young's modulus, and work of rupture in knitted fabric structures significantly reduced the standard deviations for mechanical responses. This information holds particular significance as it pertains to the frequent use of these knitted fabric structures as reinforcement in textile-reinforced composite materials. Overall, this study sheds light on the mechanical behavior in structures of knitted fabrics used in polymeric matrix composites, providing valuable insights for the design and optimization of advanced textile-based materials.

Attempt to identify antimicrobial Tridax procumbens (TP) mechanical properties using experimental work coupled with FEM model for biomedical applications.

Medicinal plants play a prodigious role in the wound-healing process. Tridax procumbens (TP) has been proven to show strong antimicrobial activity against Staphylococcus aureus and could heal skin infections. Identifying mechanical properties of TP in his solid state and mixed with carboxymethylcellulose (CMC) have never been studied before. In this study, fresh TP liquid extracts blended with carboxymethylcellulose (CMC) biofilm were developed through the solution casting method. The casted film was tested for tensile strength through the Universal Tensile Tester (UTT), and the results were compared with the Finite Element Numerical Model (FEM) through the FEM code developed on the ANSYS solver. The experimental mean tensile test results for pure CMC were found as follows: tensile stress at the maximum of 15.31 MPa, modulus of elasticity of 7,24 GPa, the density of 1,62 g/cm3, and Poisson's ratio of 0.22. The experimental mean tensile test results for pure CMC/TP 50% were as follows: tensile stress at the maximum of 26.2 MPa, modulus of elasticity of 2.092 GPa, and density of 1.276 g/cm3. After several iterations, the following results were found for pure TP: modulus of elasticity of 0.225 GPa, a density of 0.93 g/cm3, and Poisson's ratio of 0.4 through FEM using inverse method technique. The experimental results were compared with the FEM solutions, which were found to be very close to the experimental results. The TP/CMC bio-membrane could be applied as a good wound dressing in biomedical applications. Mechanical properties found in this paper can contribute to the valorization of TP usage in several medical curing films applications.

Isolation and characterization of agro-waste biomass sapodilla seeds as reinforcement in potential polymer composite applications.

Fillers or particulate fillers find a growing utilization as reinforcement material in polymer composites due to their ability to enhance the properties of the ensuing composites. The discarded seed in sapodilla fruit is available in abundant and the shell of the seed can be used as a reinforcing filler. The primary goal of this study is to extract and characterize the sapodilla seed shell powder (SSS) physically and chemically in order to assess its potential for reinforcement as a particulate filler in polymer composites. The sapodilla seed shell filler was characterized experimentally by Physio-chemical analysis, X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and Energy dispersive X-ray analysis (EDAX). The morphology and the filler size were determined by Scanning electron microscopy (SEM) and Particle size analysis. The thermal degradation behaviour was evaluated by Thermogravimetric analysis (TGA).

Modification of palm fiber with chitosan-AESO blend coating.

Natural fibers are available as an essential substitute for synthetic fiber in many applications. However, the sensitivity of Chinese Windmill Palm or Trachycarpus Fortune Fiber (TFF) to water causes low interfacial bonding between the matrix and the fiber and at the end reduces the mechanical properties of the composite product. Alkaline treatment improves mechanical properties and does not affect water absorption. Hence, additional treatment in the coating is required. This study uses alkaline treatment and coating modification using blended chitosan and Acrylated Epoxidized Soybean Oil (AESO). Blend coating between AESO and chitosan is performed to increase water absorption and mechanical properties. TFF water resistance improved significantly after the coating, with water absorption of the alkaline/blend coating-TFF of 3.98 % ± 0.52 and swell ability of 3.156 % ± 0.17. This indicated that blend coating had formed a cross-link of fiber and matrix after alkalization. Thus, the single fiber tensile strength increased due to the alkaline treatment, and water absorption decreased due to the coating. The combination of alkaline treatment and blend coating on TFF brings excellent properties, as shown by the increase in tensile strength in both single fiber test and composite.