Lignin Particles Research Articles

One-pot synthesis of monodisperse silver-lignin particles: Enhanced antibacterial agents against antibiotic-resistant bacteria

Lignin-based supports for metal nanoparticles (NPs) have attracted significant attention due to their abundant functional groups that facilitate NPs loading. However, many studies involve a two-step process: fabricating lignin particles and then reducing metal ions to NPs using physical energy consumption or chemical reduction. A one-step in-situ reduction method for NP synthesis on carrier surfaces, eliminating energy consumption, is needed for environmentally friendly and sustainable approach. Herein, we demonstrate that poly-l-lysine (PL) controls the self-assembly kinetics of kraft lignin (KL), and reduces silver ion (Ag+) to silver nanoparticles (AgNPs), forming highly monodisperse, co-self-assembled PL-KL particles (Ag@PL-KLPs) without chemical reducing agents or energy consumption. PL facilitated rapid KL desolvation, promoting intermolecular interactions and silver ion adsorption, followed by an efficient, separate nucleation and growth process yielded Ag@PL-KLPs approximately 270 nm in size with a narrow distribution. Notably, Ag@PL-KLPs exhibited enhanced bacteriostatic and bactericidal properties against antibiotic-resistant bacteria (ARB), including both Gram-negative and Gram-positive strains, at concentrations of 250 μg/mL. Leveraging biomass-derived lignin and this cost-effective, one-step green synthesis approach offers a sustainable method for avoiding antibiotic overuse and environmental contamination.

Facile preparation of photothermal and superhydrophobic melamine sponge for oil/water separation and anti-icing

The preparation of superhydrophobic sponges with excellent physiochemical performance, affordability, and versatility is still a big challenge. Herein, a photothermal and superhydrophobic melamine sponge has been successfully achieved by decorating lignin particles (LPs)@MXene composite onto the skeletons of melamine sponge (MS) via the self-polymerization of dopamine. The obtained superhydrophobic MS (labeled as MS@PDA/LPs@MXene) shows a water contact angle of 153.7°, and maintains surface superhydrophobicity under harsh conditions (i.e., acidic, alkaline environments, high temperatures, frictional damage, and icing/de-icing cycles). Notably, the MS@PDA/LPs@MXene exhibits an exceptional oil adsorption capacity of carbon tetrachloride up to 143.6 times of its own weight, a high separation efficiency of 99.3 %, and a retained separation efficiency of 98.9 % after 15 cyclic adsorption processes, respectively. Owing to a synergistic photothermal effect of PDA and LPs@MXene, the MS@PDA/LPs@MXene possesses a maximum surface temperature of 62.8 °C under solar irradiation (1.0 kW/m2, 1 sun), and realizes the ice-free property at a low temperature of −17.9 °C (relative humidity, 90 %) on a continuous cooling stage under solar irradiation (0.5 sun). Furthermore, the LPs@MXene composite coating can be applied on various substrates (i.e., Al sheet, Cu sheet, filter paper, carbon cloth, steel mesh and NdFeB magnet) to obtain surface superhydrophobicity, showing excellent anti-corrosion property for the permanent NdFeB magnet. Thus, this paper proposes a facile and cost-effective strategy to prepare superhydrophobic melamine sponge with multifunctional properties, and provides new insights into the rational design of high-performance superhydrophobic sponges for their applications in oil/water separation and anti-icing.

Characterization and structural analysis of alcohol-fractionated lignin biofuels processed at ambient temperature

This study introduces Cold-processed Lignin in (M)ethanol Oil (CLEO/CLiMO), a novel biofuel technology derived from the alcohol-fractionation of lignin at ambient temperatures, offering a sustainable alternative to conventional marine fuels. The production process achieved solid loadings of up to 60 wt% lignin and a volumetric energy density 39 % higher than pure alcohols. Lignin concentrations above 30 wt% promoted colloidal stability through the proposed formation of a spanning network of lignin aggregates, associated with a 100-fold increase of viscosity. Additionally, we observed a decrease in the radius of gyration of lignin particles from 2.5 to 2.7 nm at 30 wt% to 1.1–1.3 nm at 60 wt% following a transition from globular to elongated random coil shaped particles. This was accompanied by a twofold increase in the partial specific volume of lignin, suggesting a reduction in packing efficiency. The study highlights CLEO's potential as a sustainable shipping fuel alternative, combining favorable fuel properties with a simple and scalable production method.

Non-fluorinated lignin-based melamine sponges with superhydrophobic and photothermal properties for multi-functional applications

Frequent oil spills and the discharge of oily wastewaters become a significant threat to the environment and ecosystem. Herein, a non-fluorinated lignin-based melamine sponge with superhydrophobic and photothermal properties (labeled as MS@COF/LPs/PDMS) has been achieved by decorating with covalent organic framework (COF), lignin particles (LPs) and PDMS. The MS@COF/LPs/PDMS shows excellent surface superhydrophobicity with a water contact angle of 152.3° and a sliding angle of 6°. The adsorption capacities of the MS@COF/LPs/PDMS range from 38.4 g/g to 100.3 g/g for various oils and organic solvents, and the separation efficiency of the MS@COF/LPs/PDMS for CCl4 reaches 99.7 %. Furthermore, the maximum surface temperature of the MS@COF/LPs/PDMS reaches 61.2 °C because of the thermal vibration of LPs and COF under solar irradiation (1.0 kW/m2). Surprisingly, the MS@COF/LPs/PDMS can rapidly adsorb a droplet of crude oils within 32 s due to the superoleophilicity and excellent photothermal effect. Besides, the melting time of the MS@COF/LPs/PDMS (400 s) reduces by 70 % for an ice droplet under solar irradiation than that of pristine melamine sponge (1330 s). Thus, this study provides new insights into the rational design of low-cost lignin-based melamine sponges for the applications of oil/water separation, crude oil recovery, and de-icing.

Cold plasma/alkaline pretreatment facilitates corn stalk fractionation and valorization towards zero-waste approach

The present study employed alkaline hydrogen peroxide pretreatment coupled with cold plasma for corn stalk’s complex biopolymers fractionation and valorization through enzymatic hydrolysis. This hurdle approach enables the prolonged generation of reactive oxidative species, initiating chemical reactions otherwise hardly possible under ambient conditions. A delignification rate between 76±1 and 86±2 % was obtained under different process parameters in a significantly shorter time compared to conventional alkaline pretreatment. Up to 94±4 % of cellulose in treated biomass was converted to glucose after enzymatic hydrolysis, achieving around 3.5 times higher glucose yield than the raw biomass. Different spectroscopic analyses confirmed specific alterations in the structure of the lignin-rich fraction caused by cold plasma. Micro- and nanoscale lignin particles obtained were rich in total phenolic content, reaching up to 140±20 and 107±12 µg gallic acid equivalents (GAE) per mg of lignin, respectively. The proposed concept of corn stalk fractionation through biorefinery can open new opportunities for valorizing different agricultural waste types.

Utilizing kraft lignin–derived hard carbon as an innovative bio-electrode in electrochemical capacitors

AbstractIn recent years, biomaterials are gaining popularity due to high need to make energy storage devices greener and safer. After the carbonization process, lignin has a slightly larger specific surface and a porous structure, which can provide a significant electrochemical double-layer capacity. When combined with kraft lignin as a binder, which helps maintain the structural integrity of the electrode, the efficient use of the active material can be enhanced. The binder facilitates better dispersion of carbonized lignin particles, reducing agglomeration and ensuring greater availability of active sites for electrolyte ions. The aim of this work is to present a novel lignin-based hard carbon as an electrode material for applications in electrochemical capacitors. To this end, a detailed physicochemical and electrochemical analysis was conducted. Kraft lignin was carbonized at temperatures ranging from 600 to 1000 °C. The resulting material is characterized by thermal stability, a low polydispersion index (PDI), and mesoporosity. Thermogravimetric (TG) analysis was used to determine changes in structure, while functional groups were analyzed using Fourier-transform infrared spectroscopy (FTIR). In electrochemical applications, the material exhibits high cyclic stability and no redox reactions, with the primary mechanism of charge accumulation being based on the electrochemical double layer. Additionally, low resistances contribute to improved charge storage. Graphical abstract

Effect of Lignin Particle Size on the Properties of Cellulose Nanofiber/Lignin Composite Sheets

AbstractCellulose and lignin have been widely studied to develop a bio‐based alternative to replace fossil‐based packaging materials and coatings. Lignin can be used to improve the water vapor barrier properties of cellulose‐based sheets due to its hydrophobicity. In this study, composite sheets based on cellulose nanofiber (CNF) and lignin are formed via spray deposition the effects of lignin particle size and concentration on the properties of the composite sheets are investigated. Scanning electron microscopy and atomic force microscopy with infrared spectroscopy analysis show that lignin nanoparticles (LNPs, particle diameter <100 nm) migrate to the top surface during drying to form a dense layer. The water vapor permeability of the sheet including LNPs is reduced to 4.5 × 10−11 g·s−1·m−1·Pa−1, which is ≈20% lower than the value for CNF alone. This improvement is related to the dense LNP layer on the top surface. Water contact angle measurements indicate that the layer of LNPs also increases the surface hydrophobicity. Overall, this study provides a simple process to produce a fully bio‐based option for packaging material with enhanced water vapor barrier properties and surface hydrophobicity.

Colloidal lignin particle reinforces the stability of Pickering emulsions prepared with zein nanoparticle

Zein nanoparticle (ZNP) is at the forefront of research on Pickering emulsions, valued for its self-assembling and surfactant-free nature. Nevertheless, its emulsion stability is undermined by inadequate amphiphilicity. Colloidal lignin particle (CLP), characterized by its antithetical charge and amphiphilic nature, appears the promising for augmenting the stability of ZNP-based emulsion. This study meticulously investigated the impact of CLP on the colloidal properties and emulsifying performance of ZNP. The results revealed that electrostatic interactions between ZNP and CLP significantly mitigated the charge of ZNP and improved its hydrophilic/lipophilic balance. Under optimized conditions (1.0 wt% particle concentration, pH 4.0, 50% oil content), CLP notably reduced droplet sizes (41–225 μm) and enhanced the stability of ZNP-based Pickering emulsion, particularly at ZNP/CLP ratios of 6:4 and 5:5. In nature, CLP improved the stability ZNP-based Pickering emulsions via increased interfacial adsorption, enhanced steric hindrance, and reinforced viscous structure.

Pickering emulsion via interfacial assembly of lignin particles and cationic surfactant: Formation of robust anchoring layer

Lignin, a byproduct of the paper and pulp industry, shows promise as stabilizers for emulsions, offering potential value-added applications to direct disposal. However, utilizing particulate lignin directly as stabilizers is challenging due to limited emulsion stability. In this study, co-stabilization of Pickering emulsions is investigated by combination of lignin particles and cationic surfactants (CTAB and DDAB), wherein lignin source and oil types are optimized with a focus on emulsion stability. A battery of characterization methods, including visual appearance, microstructure, droplet size, zeta potential, etc., is employed to evaluate emulsion stability. The findings reveal that kraft lignin nanospheres (LNS) are the optimal stabilizing particles. The incorporation of cationic surfactants via electrostatic adsorption enhances the stabilizing effect of LNS, and the use of DDAB is found to significantly enhance emulsion stability compared to CTAB, attributing to higher charge shielding capability of DDAB, as well as the formation of a more robust and compact nonpolar anchoring layer. The surfactant-assisted LNS can be used to stabilize a range of oil types, with tridecane as the optimal oil. This research presents a straightforward, efficient, and scalable approach for producing highly stable lignin-based Pickering emulsions, showing potential applications in recycling and value enhancement of waste lignin.

Pickering emulsion stabilization with colloidal lignin is enhanced by salt-induced networking in the aqueous phase

We study the effect of electrolytes on the stability in aqueous media of spherical lignin particles (LP) and its relevance to Pickering emulsion stabilization. Factors considered included the role of ionic strength on morphology development, LP size distribution, surface charge, interfacial adsorption, colloidal and wetting behaviors. Stable emulsions are formed at salt concentrations as low as 50 mM, with the highest stability observed at a critical concentration (400 mM). We show salt-induced destabilization of LP aqueous dispersions at an ionic strength >400 mM. At this critical concentration LP flocculation takes place and particulate networks are formed. This has a profound consequence on the stability of LP-stabilized Pickering emulsions, affecting rheology and long-term stability. The results along with quartz microgravimetry and confocal microscopy observations suggest a possible mechanism for stabilization that considers the interfacial adsorption of LP at oil/water interfaces. The often-unwanted colloidal LP destabilization in water ensues remarkably stable Pickering emulsions by the effect of network formation.

Generation of a lignin-polyester coating for the corrosion protection of steel surfaces applied by atmospheric plasma spraying

The natural process of metal corrosion causes significant losses in a wide range of industries, requiring substantial efforts to contain its effects. An alternative approach to corrosion protection is the use of renewable organic coating materials. This research proposes the use of lignin-polyester blends as coating materials. Due to the abundance of functional groups in the lignin structure, it can act as corrosion inhibition centers in the coating. The coatings are deposited on stainless steel surfaces by a novel process route via atmospheric plasma powder spraying (APPS). To determine the effect of the lignin content on the corrosion performance, the specific amounts of lignin and polyester have been varied in 10 % increments from 0 % to 100 % with constant coating parameters. The as-produced coatings exhibited thicknesses that ranged from 11 μm to 30 μm, respectively for the pure lignin and polyester coatings. Additionally, scanning electron microscopy (SEM) analysis demonstrated the meltability of the lignin and polyester powder through the plasma process. Coatings containing a greater proportion of polyester exhibited superior meltability and better coverage. Furthermore, it was observed that the APPS promoted cross-linking of the lignin particles, as determined by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). This, in conjunction with well-balanced lignin-polyester ratios, was instrumental in achieving advanced corrosion resistance as evidenced by Potentiodynamic polarization measurement (PDP). The lignin proportion between 40 % and 60 % produced the highest corrosion inhibition efficiency, with a maximum inhibition of 96 %. Furthermore, pull-off adhesion tests suggest that lignin contributes to the overall cohesive strength of the blend.

Lignin microcapsules prepared on the basis of flexible skeleton with high foliar retention and UV shielding properties

Lignin-based microcapsules are extremely attractive for their biodegradability and photolysis resistance. However, the water-soluble all-lignin shells were unsatisfactory in terms of rainfall and foliar retention, and lacked the test of agricultural production practices. Herein, a novel microcapsule based on a flexible skeleton formed by interfacial polymerization and absorbed with lignin particles (LPMCs) was prepared in this study. Further analysis demonstrated that the shell was formed by cross-linking the two materials in layers and showed excellent flexibility and photolysis resistance. The pesticide loaded LPMCs showed about 98.68 % and 73.00 % improvement in scour resistance and photolysis resistance, respectively, as compared to the bare active ingredient. The foliar retention performance of LPMCs was tested in peanut plantations during the rainy season. LPMCs loaded with pyraclostrobin (Pyr) and tebuconazole (Teb) exhibited the best foliar disease control and optimum plant architecture, resulting in an increase in yield of about 5.36 %. LPMCs have a promising application prospect in the efficient pesticide utilization, by controlling its deformation, adhesion and release, an effective strategy for controlling diseases and managing plant growth was developed.

Self-Formation of Lignin Particles Through Melt-Extrusion for Active Biodegradable Food Packaging.

This study presents a method for the self-formation of lignin particles within a polylactic acid (PLA) matrix during melt-extrusion, eliminating the need for separation and drying steps typically associated with submicro-size lignin particles. This method effectively mitigates the problem of agglomeration often associated with the drying step. Softwood kraft lignin, guaiacyl lignin (GL-lignin), was dissolved in low-molecular-weight poly(ethylene glycol) (PEG) and was introduced into a twin-screw extruder using a liquid feeder. Lignin particles within a particle size range of 200-500 nm were observed in the extrudate of the PLA/PEG/GL-lignin composites. PLA/PEG/GL-lignin composite films were produced through blown film extrusion. These composite films demonstrated superior ultraviolet (UV)-barrier and antioxidant properties compared to neat PLA films, with optical and mechanical characteristics comparable to those of neat PLA. Moreover, migration values of the composite films in various food simulants were below regulatory limits, suggesting their potential for food packaging applications. This self-formation process offers a promising approach for utilizing lignin for PLA applications.

Multifunctional Super-Hydrophilic MXene/Biomass Composite Aerogel Evaporator for Efficient Solar-Driven Desalination and Wastewater Treatment.

Solar-driven interfacial evaporation is recognized as a sustainable and effective strategy for desalination to mitigate the freshwater scarcity issue. Nevertheless, the challenges of oil contamination, salt accumulation, and poor long-term stability of the solar desalination process limit its applications. Herein, a 3D biomass-based multifunctional solar aerogel evaporator is developed for water production with fabricated chitosan/lignin (CSL) aerogel as the skeleton, encapsulated with carbonized lignin (CL) particles and Ti3C2TiX (MXene) nanosheets as light-absorbing materials. Benefitting from its super-hydrophilic wettability, interconnected macropore structure, and high broadband light absorption (ca. 95.50%), the prepared CSL-C@MXene-20mg evaporator exhibited a high and stable water evaporation flux of 2.351kg m-2 h-1 with an energy conversion efficiency of 88.22% under 1 Sun (1kW m-2) illumination. The CSL-C@MXene-20mg evaporator performed excellent salt tolerance and long-term solar vapor generation in a 3.5wt.% NaCl solution. Also, its super-hydrophilicity and oleophobicity resulted in superior salt resistance and anti-fouling performance in high salinity brine (20wt.% NaCl) and oily wastewater. This work offers new insight into the manufacture of porous and eco-friendly biomass-based photothermal aerogels for advanced solar-powered seawater desalination and wastewater purification.

Modulation of physicochemical and antioxidant properties of Pickering emulsions using colloidal lignin particles based on kraft softwood and hardwood acetone fractions

Colloidal lignin particles (CLPs) emerge as a sustainable alternative to traditional, fossil-based emulsion stabilizers. However, effectively outperforming the conventional ingredients requires addressing the challenges posed by lignin heterogeneity and structural complexity. In this study, one-step acetone fractionation was applied to softwood and hardwood kraft lignins to tackle the issue. The resulting soluble (AS) and insoluble (AI) fractions, along with the pristine lignins, underwent thorough characterization and were used to create CLPs through the hydrotropic precipitation. The acetone fraction-derived CLPs were tested for the first time as Pickering stabilizers. Notably, a strong correlation emerged between the structural traits of each lignin sample and the properties of the resulting Pickering emulsions. Such correlation allowed for a fine-tuning of their physicochemical and antioxidant features. The AS fractions, characterized by higher phenolic OH content and lower molecular weight, led to CLPs with larger sizes and reduced hydrophilic character compared to those derived from AI- and pristine lignins. The fraction-derived CLPs exhibited superior emulsifying capacity and imparted long-term stability to the formed emulsions. Moreover, the resulting Pickering emulsions showed high potential as antioxidant agents, proving their ability as multifunctional systems. Overall, this work demonstrates how the unique properties of lignin can be selectively enhanced through acetone fractionation method and seamlessly transferred to Pickering emulsions. This advancement promotes the use of lignin in high-value-added sectors such as cosmetics and personal care.

Acid-catalyzed phenolation of lignin with tea polyphenol: Enhancing uv resistance and oxidation resistance for potential applications

The rapid development of the industry has led to the destruction of the earth's ozone layer, resulting in an increasingly serious problem of excessive ultraviolet radiation. Exploring effective measures to address these problems has become a hot topic. Lignin shows promise in the design and preparation of anti-ultraviolet products due to its inherent properties. However, it is important to investigate way to enhance the reactivity of lignin and determine its application form in related products. In this study, phenolic reactions with tea polyphenols were conducted through acid-catalyzed conversion, utilizing organic solvent lignin as the primary material. The phenolic hydroxyl content of the original lignin increased significantly by 218.8 %, resulting in notable improvements in UV resistance and oxidation resistance for phenolic lignin. Additionally, micro-nanocapsule emulsions were formed using phenolic lignin particles as surfactants through ultrasonic cavitation with small-molecule sunscreens. A bio-based sunscreen was prepared with phenolated lignin micro-nanocapsules as the active ingredient, achieving an SPF 100.2 and demonstrating excellent stability. The sunscreen also exhibited strong antioxidant properties and impermeability, ensuring user safety. This research offers a current solution for improving the application of lignin in sunscreens while also broadening the potential uses of plant-based materials in advanced functional products.

Epoxidized technical Kraft lignin as a particulate resin component for high-performance anticorrosive coatings

Deterioration of steel infrastructures is often caused by corrosive substances. In harsh conditions, the protection against corrosion is provided by high-performance coatings. The major challenge in this field is to find replacements for the fossil-based resins constituting anticorrosive coatings, due to increasing needs to synthesize new environmentally friendly materials. In this study, softwood Kraft lignin was epoxidized with the aim of obtaining a renewable resin for anticorrosive coatings. The reaction resulted in the formation of heterogeneous, solid, coarse agglomerates. Therefore, the synthetized lignin particles were mechanically ground and sieved to break up the agglomerates and obtain a fine powder. To reduce the use of fossil fuel-based epoxy novolac resins in commercial anticorrosive coatings, a series of formulations were prepared and cured on steel panels varying the content of epoxidized lignin resin. Epoxidized lignin-based coatings used in conjunction with conventional epoxy novolac resin demonstrated improved performance in terms of corrosion protection and adhesion properties, as measured by salt spray exposure and pull-off adhesion test, respectively. In addition, the importance of size fractionation for the homogeneity of the final coating formulations was highlighted. The findings from this study suggest a promising route to develop high-performing lignin-based anticorrosive coatings.

Acrylonitrile‐butadiene‐lignin thermoplastic rubber adhesive for enhanced metal‐to‐metal joining

AbstractWith the growing requirement for lightweight structural materials in automotive, aerospace, and infrastructure applications, multi‐material joints made with adhesive have attracted intense research interest. Commercial thermoset adhesives are one‐time cures, and difficult to disassemble the bonded components for repair and recycling. Our prior work with a thermoplastic acrylonitrile‐butadiene‐lignin rubber (ABL) addresses this sustainability/recycling challenge, but the adhesive exhibits deficient joining strength compared to standard thermosets. Here, we modify the ABL matrix by loading particulate fillers to enhance its modulus and toughness. The goal is to manufacture a cure‐free thermoplastic adhesive system with a simple dispensing protocol and characteristic ductility combined with a high yield stress for improved shear strength of a bonded joint. Fumed silica (FS) and epoxidized glass spheres (EGS) were used as fillers in the ABL to promote the dispersion of lignin particles that tailored the functionalities and free energy components of the adhesive surface. With optimal loading of FS (5 wt%) and EGS (30 wt%) in the ABL adhesive matrix, the lap‐shear strength of the bonded aluminum joint was elevated by 128%, compared to the neat ABL, reaching 21 MPa, which is 90% of the performance of a commercial epoxy‐based adhesive.Highlights A partly renewable filler‐toughened thermoplastic adhesive has been developed. This thermoplastic gives nearly equivalent performance of adhesively bonded aluminum joint compared to standard thermosets. Experimental and simulation data help understand the adhesive reinforcing mechanism by the fillers.

Facile Preparation of Photothermal Superhydrophobic Melamine Sponge Decorated with MXene and Lignin Particles for Efficient Oil/Water Separation, Fast Crude Oil Recovery, and Active Deicing.

Frequent oil spills and the discharge of oily wastewaters have caused a serious threat to the environment, ecosystems, and human beings. Herein, a photothermal and superhydrophobic melamine sponge (MS) decorated with MXene and lignin particles has been prepared for the separation of oil/water mixtures, the recovery of crude oils, and active deicing. The obtained superhydrophobic melamine sponge shows a water contact angle (WCA) of 152.3° and an oil contact angle of ∼0° and possesses good chemical stability, thermal stability, and mechanical durability in terms of being immersed in various liquids (i.e., corrosive solutions, organic solvents, and boiling water) and being abrased by sandpapers. This superhydrophobic MS displays a high oil adsorption capacity of CCl4, up to 91.6 times its own weight and a high separation efficiency of 99.4%. Furthermore, the maximum surface temperature of the superhydrophobic MS reaches 57.5 °C under sunlight irradiation (1.0 kW/m2) due to the excellent photothermal heating conversion performance of MXene and lignin particles. When exposed to sunlight, the superhydrophobic MS can quickly absorb viscous crude oils up to 72 times its own weight. Also, the WCA of the superhydrophobic MS remains above 146° after 50 icing/deicing cycles, showing excellent photothermal anti-icing properties. Thus, this study presents an easy and low-cost method for designing photothermal superhydrophobic melamine sponges and opens a new avenue to the applications of efficient oil/water separation, fast crude oil recovery, and active deicing.

Lignosulfonate/silica hybrid nanoparticles as a novel biobased filler in polybenzoxazine matrix

AbstractLignin is an abundant and sustainable resource that exhibits numerous attractive functional properties as a reinforcing agent for benzoxazine‐based composites, due to its stiffness, thermal stability, and high carbon content. However, the low quality of lignin particles dispersions associated with the weak particles‐matrix interactions reduces the reinforcement capability. In this work, hybrid lignin/silica (NaLS/SiO2) nanoparticles were obtained from sodium lignosulfonate (NaLS) and tetraethylorthosilicate (TEOS) under basic conditions. The particles were characterized by transmission electron microscopy (TEM) confirming their spherical morphology and narrow nanometric‐size distributions. The hybrid particles were incorporated into conventional benzoxazine (BA‐a) and a difuran biobased benzoxazine (SA‐dfda) to prepare nanocomposites with different mass compositions (3, 5, and 10 wt%). Morphological, mechanical, dynamo‐mechanical, and thermal properties of the obtained composites were assessed. All the materials exhibited a homogenous filler dispersion that contributed to improve the reinforcement properties. Hybrid nanoparticles proved to be an interesting alternative as a filler in the benzoxazine matrix to prepare high‐performance thermosetting composites.