Search Results (23)

This research work focused on the development of an adsorbent biocomposite material based on polyhydroxybutyrate (PHB) and cellulose acetate derived from sugarcane (Saccharum officinarum) fibre, through cellulose acetylation. The resulting material represents both an accessible and effective alternative for the treatment and remediation of water contaminated with heavy metals, such as Ni (II). The biocomposite was prepared by blending cellulose acetate (CA) with the biopolymer PHB using the solvent-casting method. The resulting biocomposite exhibited a point of zero charge (pHpzc) of 5.6. The material was characterised by FTIR, TGA-DSC, and SEM analyses. The results revealed that the interaction between Ni (II) ions and the biocomposite is favoured by the presence of functional groups, such as –OH, C=O, and N–H, which act as active adsorption sites on the material’s surface, enabling efficient interaction with the metal ions. Adsorption kinetics studies revealed that the biocomposite achieved an optimal adsorption capacity of 5.042 mg/g at pH 6 and an initial Ni (II) concentration of 35 mg/L, corresponding to a removal efficiency of 86.44%. Finally, an analysis of the kinetic and isotherm models indicated that the experimental data best fit the pseudo-second-order kinetic model and the Freundlich isotherm. Full article

The nonwoven industry is undergoing significant changes, driven by rapid growth and sustainability concerns, with a growing need to shift from fossil-based polymers like polyester (PES) and polypropylene (PP) fibres to biodegradable, fossil-free materials. Compared to other cellulose-based fibres, lyocell (LY) is a promising solution due to its good mechanical performance and lower environmental impact. Additionally, cellulose acetate (CA) fibres, known for their thermoplastic and biodegradable properties, can act as a binder, offering another promising alternative to fossil-based fibres. This study explores the use of 100% LY fibres, alone and in blends with CA and recycled polyester (rPES) fibres, in the development of needle-punched nonwovens and assesses the mechanical benefits of adding a thermal bonding step. Among the blends, rPES-based nonwovens with thermal bonding showed the best results. 100% LY exhibited the best mechanical performance among needle-punched nonwovens, while rPES-based blends outperformed the others. Biodegradability and toxicity studies were also performed. 100% LY nonwovens fully biodegraded within 55 days, and 100% CA and 100% rPES showed no biodegradation. The findings revealed that the thermal process did not affect the disintegration level and, the germination of Brassica oleracea was not affected by soils in which the samples were buried for 75 days. Full article

Rapid urbanisation and industrialisation have intensified the Urban Heat Island (UHI) effect, significantly increasing energy demand for thermal comfort. Urban buildings consume considerable energy throughout the year, which can be reduced by incorporating Phase Change Materials (PCMs) into building materials. PCMs effectively regulate temperature by storing and releasing heat as latent heat during phase transitions. However, to prevent leakage, PCMs can be encapsulated in co-axial polymeric Phase Change Fibres (PCFs), representing an innovative approach in scientific research. This study optimised the coagulation bath and produced PCFs using commercial cellulose acetate as the sheath and polyethylene glycol (PEG 600 and 1000) as the core via the wet-spinning method. The first part of this work investigated the coagulation bath using Attenuated Total Reflectance-Fourier Transform Infrared Spectroscopy (ATR-FTIR) analyses of the characteristic peak areas. In contrast, the second part examined the PCFs’ morphological, chemical and thermal properties using Bright-field microscopy, ATR-FTIR, Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA) techniques. The results demonstrated the successful production of PCFs with an optimised coagulation bath. Bright-field microscopy and ATR-FTIR confirmed the well-defined morphology and the presence of PEG in the fibre core. TGA analysis showed high thermal stability in the PCFs, with mass loss observed at high degradation temperatures, ranging from ~264 °C to 397 °C for the PCFs with PEG 600 and from ~273 °C to 413 °C for the PCFs with PEG 1000. Meanwhile, DSC analysis revealed melting points of ~12.64 °C and 11.04 °C, with endothermic enthalpy of ~39.24 °C and 30.59 °C and exothermic enthalpy of ~50.17 °C and 40.93 °C, respectively, for PCFs with PEG 600, and melting points of ~40.32 °C and 41.13 °C, with endothermic enthalpy of ~83.47 °C and 98.88 °C and exothermic enthalpy of ~84.66 °C and 88.79 °C, respectively, for PCFs with PEG 1000. These results validate the potential of PCFs for applications in building materials for civil engineering, promoting thermal efficiency and structural stability. Full article

This study explores a method that has the potential to be cost effective in inhibiting biofilm formation on metallic prostheses, thereby preventing rejection or the requirement for replacement. A cost-effective metal alloy used in biomedical implants was chosen as the substrate, and ibuprofen (Ibu), a well-known anti-inflammatory drug, was selected for drug release tests for its widespread availability and accessibility. Multilayer coatings consisting of cellulose acetate (CA), polycaprolactone (PCL), and chitosan (CHI), with or without ibuprofen (Ibu) content, were applied onto medical-grade stainless steel (SS-316 type) through electrospinning, electrospray, or blow spinning. The adhesion of the CA, PCL, and layered CA/PCL membranes, with thicknesses ranging from 20 to 100 μm, to SS substrates varied between 0.15 N and 0.22 N without CHI, which increased to 0.21 and 0.74 N, respectively, when a CHI interlayer was introduced by electrospraying between the SS and the coatings. Although drug release in a simulated body fluid (SBF) medium is predominantly governed by diffusion-driven mechanisms in all single- and multilayer coatings, a delayed release was noted in CA coatings containing Ibu when overlaid with a PCL coating produced by blow spinning. This suggests avenues for further investigations into combinations of multilayer coatings, both with and without drug-imbued layers. Full article

Cellulose/silica nanocomposites, synthesised through the sol–gel technique, have garnered significant attention for their unique properties and diverse applications. The distinctive characteristics of these nanocomposites are influenced by a range of factors, including the cellulose-to-silica ratio, precursor concentration, pH, catalysts, solvent selection, temperature, processing techniques, and agitation. These variables play a pivotal role in determining the nanocomposites’ structure, morphology, and mechanical properties, facilitating tailoring for specific applications. Studies by Raabe et al. and Barud et al. demonstrated well-deposited silica nanoparticles within the interstitial spaces of cellulosic fibres, achieved through TEOS precursor hydrolysis and the subsequent condensation of hydroxyl groups on the cellulose fibre surface. The introduction of TEOS established a robust affinity between the inorganic filler and the polymer matrix, emphasising the substantial impact of TEOS concentration on the size and morphology of silica nanoparticles in the final composites. The successful functionalisation of cellulose fibres with the TEOS precursor via the sol–gel method was reported, resulting in reduced water uptake and enhanced mechanical strength due to the strong chemical interaction between silica and cellulose. In research conducted by Feng et al., the silica/cellulose composite exhibited reduced weight loss compared to the pristine cellulose matrix, with the integration of silica leading to an elevated temperature of composite degradation. Additionally, Ahmad et al. investigated the effects of silica addition to cellulose acetate (CA) and polyethylene glycol membranes, noting an increase in Young’s modulus, tensile strength, and elongation at break with silica incorporation. However, concentrations exceeding 4% (w/v) resulted in significant phase separations, leading to a decline in mechanical properties. Full article

Nowadays, the growing concern about improving thermal comfort in different structures (textiles, buildings, and pavements, among others) has stimulated research into phase change materials (PCMs). The direct incorporation of PCMs into composite materials can cause mechanical impacts. Therefore, this study focuses on the design of phase change coaxial fibres (PCFs), using commercial cellulose acetate (CA) or recycled CA obtained from cotton fabrics (CAt) as the sheath and polyethylene glycol (PEG) 2000 as the core, via the wet spinning method; the fibres vary in molecular weight, concentration and ejection velocity. The fibres were assessed for their optical, chemical, thermal, and mechanical properties. The presence of PEG2000 is confirmed in the core of the fibres. Thermal analyses revealed a mass loss at high temperatures, attributable to the presence of PEG2000. Notably, the fibres with CA (Mn 30,000) showed superior thermal and mechanical performance. The melting point of PEG2000 incorporated into these PCFs coincided with the melting point of pure PEG2000 (about 55 °C), with a slight deviation, indicating that PCFs were obtained. Finally, the results point to the application of the fibres in civil engineering materials requiring a phase change between 50 and 60 °C, providing promising prospects for their use in applications requiring thermoregulatory properties. Full article

Bast fibre-reinforced plastics are characterised by good strength and stiffness but are often brittle due to the stiff and less ductile fibres. This study uses a biomimetic approach to improve impact strength. Based on the structure of the spicules of a deep-sea glass sponge, in which hard layers of bioglass alternate with soft layers of proteins, the toughness of kenaf/epoxy composites was significantly improved by a multilayer structure of kenaf and cellulose acetate (CA) foils as impact modifiers. Due to the alternating structure, cracks are deflected, and toughness is improved. One to five CA foils were stacked with kenaf layers and processed to composite plates with bio-based epoxy resin by compression moulding. Results have shown a significant improvement in toughness using CA foils due to increased crack propagation. The unnotched Charpy impact strength increased from 9.0 kJ/m² of the pure kenaf/epoxy composite to 36.3 kJ/m² for the sample containing five CA foils. The tensile and flexural strength ranged from 74 to 81 MPa and 112 to 125 MPa, respectively. The tensile modulus reached values between 9100 and 10,600 MPa, and the flexural modulus ranged between 7200 and 8100 MPa. The results demonstrate the successful implementation of an abstract transfer of biological role models to improve the toughness of brittle bast fibre-reinforced plastics. Full article

Worldwide, the need for thermal insulation materials used to increase the energy performance of buildings and ensure indoor thermal comfort is constantly growing. There are several traditional, well-known and frequently used thermal insulation materials on the building materials market, but there is a growing trend towards innovative materials based on agro-industrial waste. This paper analyses the performance of 10 such innovative thermal insulation materials obtained by recycling cellulosic and/or animal waste, using standardised testing methods. More precisely, thermal insulation materials based on the following raw materials were analysed: cellulose acetate, cigarette filter manufacturing waste; cellulose acetate, cigarette filter manufacturing waste and cigarette paper waste; cellulose acetate, waste from cigarette filter manufacturing, waste cigarette paper and waste aluminised paper; cellulose from waste paper (two types made by two independent manufacturers); wood fibres; cellulose from cardboard waste; cellulose from waste cardboard, poor processing, inhomogeneous product; rice husk waste and composite based on sheep wool, recycled PET fibres and cellulosic fibres for the textile industry. The analysis followed the performance in terms of thermal insulating quality, evidenced by the thermal conductivity coefficient (used as a measurable indicator) determined for both dry and conditioned material at 50% RH, in several density variants, simulating the subsidence under its own weight or under various possible stresses arising in use. The results showed in most cases that an increase in material density has beneficial effects by reducing the coefficient of thermal conductivity, but exceptions were also reported. In conjunction with this parameter, the analysis of the 10 types of materials also looked at their moisture sorption/desorption capacity (using as a measurable indicator the amount of water stored by the material), concluding that, although they have a capacity to regulate the humidity of the indoor air, under low RH conditions the water loss is not complete, leaving a residual quantity of material that could favour the development of mould. Therefore, the impact on indoor air quality was also analysed by assessing the risk of mould growth (using as a measurable indicator the class and performance category of the material in terms of nutrient content conducive to the growth of microorganisms) under high humidity conditions but also the resistance to the action of two commonly encountered moulds, Aspergillus niger and Penicillium notatum. The results showed a relative resistance to the action of microbiological factors, indicating however the need for intensified biocidal treatment. Full article

Controlled drug release via electrical stimulation from drug-impregnated fibres was studied using electrospun cellulose acetate (CA) membranes and encapsulated ibuprofen (IBU). This research outlines the influence of polypyrrole (PPy) and poly(3,4-ethylenedioxythiophene) (PEDOT)-functionalised CA membranes and their suitability for dermal electronic-controlled drug release. Micro Raman analysis confirmed polymer functionalisation of CA membranes and drug incorporation. Scanning electron microscopy (SEM) images evidenced the presence of PPy and PEDOT coatings. The kinetic of drug release was analysed, and the passive and active release was compared. In the proposed systems, the drug release is controlled by very low electrical potentials. A potential of −0.3 V applied to membranes showed the ibuprofen retention, and a positive potential of +0.3 V, +0.5 V, or +0.8 V, depending on the conductive polymer and membrane configuration, enhanced the drug release. A small adhesive patch was constructed to validate this system for cutaneous application and verified an “ON/OFF” ibuprofen release pattern from membranes. Full article

In this study, elementary kenaf fibres were separated from fibre bundles using two different treatments. The first involved treating with nitric acid (HNO₃) while the second used a mixture of hydrogen peroxide (H₂O₂) and acetic acid (CH₃COOH). Both treatments were successful in isolating the elementary fibres but the H₂O₂/CH₃COOH gave a better fibre yield and required a shorter treatment time. The fibres treated with HNO₃ had an average length of 0.2 mm, an aspect ratio of 15 and a defect density of 21 defects per mm. In contrast, the H₂O₂/CH₃COOH treated fibres had a length of 2.3 mm, an aspect ratio of 179 and a defect density of 14 defects per mm. Both treatments removed lignin, pectin, and waxes. They also increased cellulose crystallinity in the fibres, especially for HNO₃ treatment. However, they resulted in some oxidation of cellulose. The H₂O₂/CH₃COOH treatment gave a substantial improvement in the thermal stability of the fibres while a marked decrease was observed for the HNO₃ treatment. Full article

Natural nanofibers are widely used in the field of medicine, but the low strength of these nanofibers is one of the major concerns. A number of factors, importantly the composition, affect the strength of natural nanofibers. The purpose of the current study is to ascertain the effect of the composition of natural nanofibers on the strength of hybrid composites formed using these nanofibers. Hybrid composites formed using 32% volume glass fibre with optimized volume fraction of 0.5% of pure Cellulose Acetate (CA), and 0.5% CA + Hemp Seed (HS) for this study to carry out the analysis. Hybrid composites were produced with vacuum-assisted resin transfer molding (VARTM) by collecting natural nanofibers, produced using the electrospinning process, over glass fiber mats. The electrospinning process was carried out with 12 kV, 10 cm tip to the collector gap, and 12% concentration of the solution. The tensile strength of the hybrid composites was measured using the universal testing machine (UTM). The results showed that the diameter of the electrospun nanofiber varied between 50 and 1400 nm and was affected by solution concentration, voltage, tip-to-collector distance, flow rate, and inclusion of HS in CA. The inclusion of HS in CA, for all compositions, decreased the fiber diameter and caused the formation of beads prominently at higher concentrations. Hybrid composites formed from nanofibers produced using CA and HS showed higher elastic modulus (232 MPa) and tensile strength (20.4 GPa) as compared with nanofibers produced using CA only (elastic modulus = 110 MPa and 13.7 GPa). Full article

This work is focused on optimising a low-temperature delignification as holocellulose purification pretreatment of Platanus acerifolia leaf waste for second-bioethanol production. Delignification was accomplished by acid-oxidative digestion using green reagents: acetic acid and 30% hydrogen peroxide 1:1. The effect of reaction time (30–90 min), temperature (60–90 °C), and solid loading (5–15 g solid/20 g liquid) on delignification and solid fraction yield were studied. The process parameters were optimised using the Box–Behnken experimental design. The highest attained lignin removal efficiency was larger than 80%. The optimised conditions of delignification, while maximising holocellulose yield, pointed to using the minimum temperature of the examined range. Analysis of variance on the solid fraction yield and the lignin removal suggested a linear model with a negative influence of the temperature on the yield. Furthermore, a negative effect of the solid loading and low effect of temperature and time was found on the degree of delignification. Then the temperature range was extended back to 60 °C, providing 71% holocellulose yield and 70% while improving energy efficiency by working at a lower temperature. Successful lignin removal was confirmed using confocal laser scanning microscopy. As evaluated by scanning electron microscopy, the solid structure presented an increased exposition of the cellulose fibre structure. Full article

Calcium phosphate (CaP)-based ceramic–biopolymer composites can be regarded as innovative bioresorbable coatings for load-bearing implants that can promote the osseointegration process. The carbonated hydroxyapatite (cHAp) phase is the most suitable CaP form, since it has the highest similarity to the mineral phase in human bones. In this paper, we investigated the effect of wet chemical preparation parameters on the formation of different CaP phases and compared their morphological and structural characteristics. The results revealed that the shape and crystallinity of CaP particles were strongly dependent on the post-treatment methods, such as heat or alkaline treatment of as-precipitated powders. In the next step, the optimised cHAp particles have been embedded into two types of biopolymers, such as polyvinyl pyrrolidone (PVP) and cellulose acetate (CA). The pure polymer fibres and the cHAp–biopolymer composites were produced using a novel electrospinning technique. The SEM images showed the differences between the morphology and network of CA and PVP fibres as well as proved the successful attachment of cHAp particles. In both cases, the fibres were partially covered with cHAp clusters. The SEM measurements on samples after one week of immersion in PBS solution evidenced the biodegradability of the cHAp–biopolymer composites. Full article

Air filters are crucial components of a building ventilation system that contribute to improving indoor air quality, but they are typically associated with relatively high pressure drops. The purpose of the study is to evaluate the effect of additives on ultrathin electrospun filters, the pressure drop, and the particle removal efficiency of uniformly charged particles. The fibres were electrospun under optimised conditions that resulted in a fast-fabricating process due to the properties of the cellulose acetate solution. Different ultrathin electrospun fibre filters based on cellulose acetate (CA) were fabricated: a pure CA electrospun fibre filter, two filters based on CA fibres separately doped with activated charcoal (AC) and titanium dioxide (TiO₂), respectively, and a composite filter where the two additives, AC and TiO₂, were embedded between two CA fibres layers. The ultrathin filters exhibited a low pressure drop of between 63.0 and 63.8 Pa at a face velocity of 0.8 m s⁻¹. The filtration performance of uniformly charged particles showed a removal efficiency above 70% for particle sizes between 0.3 and 0.5 μm for all filters, rising above 90% for larger particles between 1 and 10 μm, which translates to the average sizes of pollens and other allergenic contaminant particles. Due to the positive impact on the fibre morphology caused by the additives, the composite filter showed the highest filtration performance among the produced filters, reaching 82.3% removal efficiency towards smaller particles and a removal of up to 100% for particle sizes between 5 and 10 μm. Furthermore, cellulose acetate itself is not a source of microparticles and is fully biodegradable compared to other polymers commonly used for filters. These ultrathin electrospun filters are expected to be practical in applications for better building environments. Full article

The capacity of microbiota to produce medium-chain fatty acids (MCFA) and related consequences for the gastrointestinal (GI) tract have never been reported before. We verified the impact of nutrition-related factors on fatty acid (FAs) production and found that caloric restriction decreased levels of most of MCFAs in the mouse cecum, whereas overnight fasting reduced the levels of acetate and butyrate but increased propionate and laurate. A diet high in soluble fibre boosted the production of short-chain fatty acids (SCFA) and caproate whereas a high-cellulose diet did not have an effect or decreased the levels of some of the FAs. Rectal infusion of caprylate resulted in its rapid metabolism for energy production. Repeated 10-day MCFA infusion impacted epididymal white adipose tissue (eWAT) weight and lipid accumulation. Repeated infusion of caprylate rectally tended to increase the concentration of active ghrelin in mice plasma; however, this increase was not statistically significant. In Caco-2 cells, caprylate increased the expression of Fabp2, Pdk4, Tlr3, and Gpr40 genes as well as counteracted TNFα-triggered downregulation of Pparγ, Occludin, and Zonulin mRNA expression. In conclusion, we show that colonic MCFAs can be rapidly utilized as a source of energy or stored as a lipid supply. Further, locally produced caprylate may impact metabolism and inflammatory parameters in the colon. Full article