Search Results (85)

Wood is a green and renewable bio-based building material, but its hygroscopicity affects its dimensional stability, limiting its use in construction. Chemical modification can improve its properties, yet its effectiveness depends on wood permeability and traditional modifiers. This study first used a deep eutectic solvent (DES) to boost the permeability of North American alder wood. Then, methyl trimethoxysilane was impregnated under supercritical carbon dioxide (SCI), pressure (PI), vacuum (VI), and atmospheric pressure (AI) conditions. DES treatment damaged the cell structure, increasing wood permeability. Silane was deposited and polymerized in the cell lumen, chemically bonding with cell-wall components, filling walls and pits, and thickening walls. The VI group had the highest absolute density (0.59 g/cm³, +36.6%) and the lowest moisture absorption (4.4%, −33.3%). The AI group had the highest ASE (25%). The PI group showed the highest surface hardness (RL, 2592 N) and a water contact angle of 131.9°, much higher than natural wood. Overall, the VI group had the best performance. Silane reacts with cellulose, hemicellulose, and lignin in wood via hydrolysis and hydroxyl bonding, forming stable bonds that enhance the treated wood’s hydrophobicity, dimensional stability, and surface hardness. Full article

In the chemistry of bio-based furans, the Diels–Alder reaction plays an important role as a renewable route for the synthesis of fuels, fine chemicals, and monomers. Nonetheless, the unfavorable kinetic and thermodynamic parameters inherent to the Diels–Alder reaction involving furans as dienes often lead to the reversibility of cycloaddition, resulting in decreased equilibrium conversion and diastereoselectivity. In this study, we present a new strategy for overcoming the problem of reversibility in chemical reactions. We demonstrate that conducting the reaction under solvent-free conditions can facilitate the transition from a molten state formed by the initial reactants to a solid phase containing the reaction product along with an excess of the initial substrate. According to our results, such a liquid-to-solid transition of the reaction mixture can lead to exceptionally high conversion and diastereoselectivity in the furan–maleimide Diels–Alder reaction, particularly for challenging electron-poor furanic substrates. Our approach enables the reversible furan–maleimide Diels–Alder reaction to be performed in a cleaner and more environmentally friendly manner, free from the complexities associated with the use of solvents and the need for purification from side products. Full article

The increasing environmental concerns and regulatory restrictions on toxic conventional solvents have driven the search for sustainable alternatives. Dimethyl isosorbide (DMI), a bio-renewable solvent, has shown potential as a replacement for short-chain glycol ethers, although its use as solvent in liquid chromatography (LC) is underexplored. This study presents a physicochemical characterization of DMI with a particular focus on its application as an innovative solvent in LC analyses. The partition coefficient (log P = −0.44) was determined using the OECD 107 method, and viscosity measurements for DMI and its mixtures with water and ethanol were conducted at 25 °C, 40 °C, and 60 °C. Viscosity ranged from 1.28 mPa·s at 60 °C to 2.62 mPa·s at 40 °C. The Central Composite Face 2³ experimental design for studying the chromatographic behavior of DMI confirmed that 50% (v/v) DMI can be effectively utilized in the mobile phases, at a column temperature of 40 °C, with backpressures ranging from 160 to 300 bar and a UV cut-off at 240 nm. Its effectiveness as an eluent in LC was demonstrated for the quantification of methylparaben and propylparaben in pharmaceutical formulations. This study highlights DMI’s promise as a sustainable bio-renewable alternative to conventional organic solvents used as eluents in LC, supporting eco-friendly practices in pharmaceutical analysis. Full article

Volatile C2–C5 olefins are important bulk chemicals in the polymer industry. Traditionally, C2–C5 olefins are produced from cracked petroleum resources using an energy-consuming and hazardous distillation method. Currently, volatile olefins can be produced from renewable biomass. To obtain polymer-grade volatile olefins from diversified resources, more sustainable and feasible separation techniques need to be developed. This review focuses on two updated separation techniques for C2–C5 olefins: (a) adsorption separation, which separates olefins through porous affinity, the pi complexation effect, and size-exclusion and gate-opening sieving, and (b) liquid absorption separation, which utilizes either organic solvents or ionic liquids for olefin separation. In this review, different separation techniques are compared in terms of their mechanisms and operation conditions in the separation of different types of C2–C5 olefins from variable resources, such as cracked ethylene/propylene/butylene/isoprene and bio-isoprene. Full article

To tackle growing resource and environmental challenges, closed-loop chemical recycling of waste PET is gaining significant attention. Methanolysis demonstrates significant industrial potential due to the ease of separation and purification of its depolymerization product, dimethyl terephthalate (DMT). However, conventional methanolysis processes for PET typically require harsh conditions (>200 °C and 2–4 MPa), highlighting the need for more efficient and milder methods. In this work, leveraging Hansen’s solubility parameter theory, a bio-based solvent gamma-valerolactone (GVL) was introduced to construct a binary mixed solvent system, enabling highly efficient depolymerization of PET. Through systematic optimization of reaction conditions, an in-depth analysis of the effects of various factors on depolymerization efficiency and kinetics was conducted. The incorporation of GVL markedly enhanced the compatibility between the solvent and PET, thereby significantly improving depolymerization efficiency while effectively lowering the reaction temperature and pressure. Complete depolymerization of PET can be achieved within 2 h at 150 °C under a pressure of 0.9 MPa, with a DMT yield of up to 97.8%. This GVL/methanol depolymerization system exhibits higher efficiency, milder reaction conditions, and substantial advantages in terms of environmental impact and energy consumption indicators. By using the renewable bio-based solvent GVL, this technology aligns with the core principles of green chemistry and provides an efficient, feasible, and innovative pathway for sustainable closed-loop PET recycling. Full article

α-Pinene is a very valuable natural raw material for organic syntheses, which is of increasing interest to scientists due to its renewability and relatively low price. This work presents the studies on the oxidation of α-pinene in the presence of two mesoporous titanium-silicate catalysts: standard Ti-SBA-15 and Ti-SBA-15 material, which was obtained by a new and green way using orange peel waste as bio-templates (Ti-SBA-15_orange peels). For the synthesis of the Ti-SBA-15 catalysts, the following raw materials were used: Pluronic P123 as the template (template usually used in the synthesis of SBA-15 materials), tetraethyl orthosilicate as the silicon source, hydrochloric acid, deionized water, and tetraisopropyl orthotitanate as the titanium source. For the synthesis of Ti-SBA-15_orange peels, a catalyst was also properly prepared, and orange peel waste as the co-templates (renewable templates) were used. The two obtained Ti-SBA-15 materials were characterized by the following instrumental methods: XRD, SEM, EDX, UV-Vis, and FTIR. Moreover, the specific surface area and pore size distribution were investigated for these catalysts with help from the nitrogen adsorption–desorption method. Catalytic tests of the obtained catalysts were performed in the oxidation of α-pinene with oxygen and by the method which did not use any solvent (α-pinene was simultaneously the raw material and solvent in this process). During the catalytic tests, the effect of temperature, catalyst content, and reaction time on the selectivities of the appropriate products and the conversion of α-pinene were studied. Depending on the conditions of the oxidation process, the catalyst obtained with the use of orange peels as co-templates showed similar or even higher activity than the standard Ti-SBA-15 catalyst. Full article

The growing interest in renewable resource-based materials has driven efforts to develop elastomeric biocomposites using biomass, phyto-ash, and biochar as fillers. These bio-additives, derived from beech wood through various processing methods, were incorporated into natural rubber (NR) at varying weight ratios. The primary objective of this study was to assess how the type and content of each bio-filler influence the structural, processing, and performance properties of the biocomposites. Mechanical properties, including tensile strength and hardness, were evaluated, while crosslink density of the vulcanizates was determined using equilibrium swelling in solvents. Additionally, the composites underwent thermogravimetric analysis (TGA) to determine the decomposition temperature of individual components within the polymer matrix. Bio-fillers influenced rheological and mechanical properties, with phyto-ash reducing viscosity and cross-linking density, and biochar and biomass increasing stiffness and maximum torque. Biochar extended curing time due to the absorption of curing agents, whereas phyto-ash accelerated vulcanization. Mechanical tests showed that all bio-filled composites were stiffer than the reference, with biochar and biomass (30 phr) exhibiting the highest hardness (45.8 °ShA and 49.1 °ShA, respectively) and cross-link density (2.68 × 10⁻⁵ mol/cm³ and 2.77 × 10⁻⁵ mol/cm³, respectively), contributing to improved tensile strength, in particular in the case of biochar, where the TS was 17.6 MPa. The study also examined the effects of thermal-oxidative aging on the samples, providing insights into the changes in the mechanical properties of the biocomposites under simulated aging conditions. Full article

Background: One of the foremost causes of microbial infections and propagation is improper sanitation and hygiene maintained in public places. Accumulation of stains and microbes results in the spread of infections. Also, due to the extensive use of non-renewable materials like petrochemicals, etc., there is an increasing demand for sustainable growth in the coating industries. Currently, there is no such technology that tackles this problem. Methods: Our present work aims to find a prolonged solution for these problems for the first time by synthesizing and formulating bio-based coatings with inherent antimicrobial properties and durable surface properties with a fast air-curing system. A formulation of alkyd and polyesteramide resins from castor, neem, and karanja oils was crosslinked with isocyanates to form the surface coatings. An esterification reaction of castor oil monoglyceride and phthalic anhydride synthesized the castor oil alkyd resin. The corresponding neem and karanja oil polyesteramides were synthesized by amidation with diethanolamine, followed by an esterification reaction. Results: The coatings exhibit an antimicrobial efficacy of 74%–84% against both Gram-positive and Gram-negative bacteria and contain 76.5% bio-based content. Factors such as thermal stability, physicochemical properties, and chemical and solvent stability were studied. After 24 h of inoculation with 40% polyesteramide resin (AMRESN-4), E. coli and S. aureus CFU values decreased from 6 × 10⁵ to 0.28 × 10⁵ CFU/g and from 5.7 × 10⁵ to 0.26 × 10⁵ CFU/g, respectively. These bio-based coatings are particularly suited for environments requiring high durability and antimicrobial protection, such as food-processing facilities, healthcare settings, and public restrooms. Full article

Conventional epoxy thermosets, with irreversible crosslinking networks, cannot be reprocessed and recycled. Furthermore, the utilization of petroleum-based materials accelerates the depletion of non-renewable resources. The introduction of dynamic covalent bonds and the use of bio-based materials for thermosets can effectively address the above issues. Herein, a series of bio-based epoxy vitrimers with dynamic covalent imine bonds were synthesized via a simple solvent-free, one-pot method using vanillin-derived aldehyde monomers, 4,4-diaminodiphenylsulfone (DDS) and bisphenol F diglycidyl ether (BFDGE) as raw materials. The effect of crosslinking density, crosslinking structure and imine bond content on the resulting bio-based vitrimers was studied, demonstrating their excellent thermal properties, UV shielding and solvent resistance, as well as outstanding mechanical properties compared to those of the previously reported vitrimers. In particular, the cured neat resin of vitrimer had a maximum tensile strength of 109 MPa and Young’s modulus of 6257 MPa, which are higher than those of previously reported imine-based vitrimers. The dynamic imine bonds endow these vitrimers with good reprocessability upon heating (over 70% recovery) and degradation under acidic conditions, enabling recycling by physical routes and gentle degradation by chemical routes. This study demonstrates a simple and effective process to prepare high-performance bio-based and recycled epoxy thermosets. Full article

Waste cooking oils (WCOs) are generated globally from households, the hospitality industry, and other sectors. Presently, WCOs are mainly employed as feedstock for biodiesel and energy production, strongly depending on the availability of WCOs, which are often imported from other countries. The objective of this review is to give an overall comprehensive panorama of the impacts, regulations, and restrictions affecting WCOs, and their possible uses for producing high-value products, such as bio lubricants, bio surfactants, polymer additives, road and construction additives, and bio solvents. Interestingly, many reviews are reported in the literature that address the use of WCOs, but a comprehensive review of the topic is missing. Published studies, industry reports, and regulatory documents were examined to identify trends, challenges, production statistics, environmental impacts, current regulations, and uses for high-value polymer production. The data collected show that WCOs hold immense potential as renewable resources for sustainable industrial applications that are in line with global carbon neutrality goals and circular economy principles. However, achieving this shift requires addressing regulatory gaps, enhancing collection systems, and optimizing conversion technologies. This comprehensive review underlines the need for collaborative efforts among policymakers, industry stakeholders, and researchers to maximize the potential of WCOs and contribute to sustainable development. Full article

Lignin is considered a renewable source for the production of valuable aromatic chemicals and liquid fuel. Solvent depolymerization of lignin is a fruitful strategy for the valorization of lignin. However, Kraft lignin is highly prone to produce char (a by-product) during the hydrothermal depolymerization process due to its poor solubility in organic solvents. Therefore, the minimization of char formation remains challenging. The purpose of the present study was to fractionate Kraft lignin in methanol to obtain low-molecular-weight fractions that could be further depolymerized in supercritical methanol to produce aromatic monomers and to suppress char formation. The results showed that the use of methanol-soluble lignin achieved a bio-oil yield of 45.04% and a char yield of 39.6% at 280 °C for 2 h compared to 28.57% and 57.73%, respectively, when using raw Kraft lignin. Elemental analysis revealed a high heating value of 30.13 MJ kg⁻¹ and a sulfur content of only 0.09% for the bio-oil derived from methanol-soluble lignin. The methanol extraction process reduced the oxygen content and increased the hydrogen and carbon contents in the modified lignin and bio-oil, indicating that the extracted lignin fraction had an enhanced deoxygenation capability and a higher energy content. These findings highlight the potential of methanol-soluble Kraft lignin as a valuable resource for sustainable energy production and the production of aromatic compounds. Full article

The significant environmental impact from fashion and textile industries has spurred interest in sustainable alternatives, especially for accessories like sequins and beads, whose usage has surged post-pandemic. This study explores the potential of utilizing salmon industry waste from Chile to produce bio-sequins (BS) and guanine crystals (GC) from salmon skin. The production of BS offers a strategy to reduce reliance on non-renewable resources and support sustainable waste management, as these materials decompose naturally without harmful residues. Physicochemical and mechanical characterization of the BS by using scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), thermogravimetric analysis (TGA), X-ray powder diffraction (XRPD), and Fourier transform infrared spectroscopy (FT-IR), evaluated their feasibility for textile, design, and fashion applications. Additionally, GC were extracted from salmon scales using less hazardous solvents such as acetone, ethanol, and acetic acid, and subsequently immobilized on the BS for decorative purposes. Notably, tensile mechanical properties of the BS improved up to 75% after guanine decoration and exposure to simulated environmental factors like UV radiation. This work addresses the dual challenge of pollution and resource depletion, demonstrating that BS from salmon skin offer an eco-friendly alternative. It underscores the importance of adopting sustainable practices throughout the fashion industry’s production chain. Full article

Achieving high-performance 3D printing composite filaments requires addressing challenges related to fibre wetting and uniform fibre/polymer distribution. This study evaluates the effectiveness of solution (solvent-based) and emulsion (water-based) impregnation techniques to enhance fibre wetting in bleached flax yarns by polylactide (PLA). For the first time, continuous viscose yarn composites were also produced using both impregnation techniques. All the composites were carefully characterised throughout each stage of production. Initially, single yarns were impregnated and consolidated to optimise formulations and processing parameters. Solution impregnation resulted in the highest tensile strength (356 MPa) for PLA/bleached flax filaments, while emulsion impregnation yielded the highest tensile strength for PLA/viscose filaments (255 MPa) due to better fibre wetting and fibre distribution. Impregnated single yarns were then combined, with additional polymer added to produce filaments compatible with standard material extrusion 3D printers. Despite a reduction in the mechanical performance of the 3D-printed composites due to additional polymer impregnation, relatively high tensile and bending strengths were achieved, and the Charpy impact strength (>127 kJ/m²) for the viscose-based composite exceeded the reported values for bio-derived fibre reinforced composites. The robust mechanical performance of these filaments offers new opportunities for the large-scale additive manufacturing of structural components from bio-derived and renewable resources. Full article

Bacterial cellulose (BC) is an advantageous polymer due to its renewable nature, low cost, environmental compatibility, biocompatibility, biodegradability, chemical stability, and ease of modification. With these advantages, BC is an interesting candidate for the development of novel eco-friendly materials for proton-exchange membrane (PEM) applications. However, its practical applications have been limited by its relatively high dispersion in water, which usually occurs during the operation of proton-exchange membrane fuel cells (PEMFCs). In addition, the proton conductivity of bacterial cellulose is poor. In this study, functionalized BC modified with 3-aminopropyltriethoxysilane (APTES) was prepared using a solvent casting method to enhance its performance. The results showed that the water stability of the modified BC membrane was significantly improved, with the contact angle increasing from 54.9° to 103.3°. Furthermore, the optimum ratio of BC and APTES was used to prepare a proton-exchange membrane with a maximum proton conductivity of 62.2 mS/cm, which exhibited a power generation performance of 4.85 mW/cm² in PEMFCs. It is worth mentioning that modified BC membranes obtained by combining an alkaline proton carrier (-NH₂) with BC have rarely been reported. As fully bio-based conductive membranes for PEMFCs, they have the potential to be a low-cost, eco-friendly, and degradable alternative to expensive, ecologically problematic fluoric ionomers in short-term or disposable applications, such as biodegradable electronics and portable power supplies. Full article

This study is focused on the modelling of the production of bio-oil by thermochemical liquefaction. Species Acacia melanoxylon was used as the source of biomass, the standard chemical 2-Ethylhexanol (2-EHEX) was used as solvent, p-Toluenesulfonic acid (pTSA) was used as the catalyst, and acetone was used for the washing process. This procedure consisted of a moderate acid-catalysed liquefaction process and was applied at 3 different temperatures to determine the proper model: 100, 135, and 170 °C, and at 30-, 115-, and 200-min periods with 0.5%, 5.25%, and 10% (m/m) catalyst concentrations of overall mass. Optimized results showed a bio-oil yield of 83.29% and an HHV of 34.31 MJ/kg. A central composite face-centred (CCF) design was applied to the liquefaction reaction optimization. Reaction time, reaction temperature, as well as catalyst concentration, were chosen as independent variables. The resulting model exhibited very good results, with a highly adjusted R-squared (1.000). The liquefied products and biochar samples were characterized by Fourier-transformed infrared (FTIR) and thermogravimetric analysis (TGA); scanning electron microscopy (SEM) was also performed. The results show that invasive species such as acacia may have very good potential to generate biofuels and utilize lignocellulosic biomass in different ways. Additionally, using acacia as feedstock for bio-oil liquefaction will allow the valorisation of woody biomass and prevent forest fires as well. Besides, this process may provide a chance to control the invasive species in the forests, reduce the effect of forest fires, and produce bio-oil as a renewable energy. Full article