Lignin Blends Research Articles

Harnessing the synergistic power of lignin-Ecoflex blends for enhanced performance in food packaging

In this study, a two-step chemical modification method was applied to lignin, enabling the thermal blending of lignin and Ecoflex® (PBAT) to produce films for food packaging applications. In the first step, 90 % of phenolic and carboxylic acid groups were converted into aliphatic hydroxy groups via hydroxyethylation, and in the second step, the aliphatic hydroxy groups were esterified with cinnamic acid, introducing abundant phenyl rings as well as unsaturated groups to the polymer. The modified lignin possessed an aliphatic–aromatic structure, similar to Ecoflex®, thereby enhancing the potential miscibility between these two materials. Subsequent experiments revealed that adding 20 % of modified lignin into Ecoflex® film resulted in the most significant improvement in mechanical properties, tripling the stiffness and doubling the strength. The addition of 30 % of modified lignin showed the best outcomes in UV absorption, barrier properties against oxygen and water vapor, and anti-oxidation ability. A strawberry ripening test indicated that the Ecoflex® film containing 30 % of modified lignin extended the shelf-life of strawberries from 2 days to 7 days, with better performance than the results of polyethylene bags and pure Ecoflex® films.

Influence of Hardwood Lignin Blending on the Electrical and Mechanical Properties of Cellulose Based Carbon Fibers.

Carbon fibers (CFs) are fabricated by blending hardwood kraft lignin (HKL) and cellulose. Various compositions of HKL and cellulose in blended solutions are air-gap spun in 1-ethyl-3-methylimidazolium acetate (EMIM OAc), resulting in the production of virtually bead-free quality fibers. The synthesized HKL-cellulose fibers are thermostabilized and carbonized to achieve CFs, and consequently their electrical and mechanical properties are evaluated. Remarkably, fibers with the highest lignin content (65%) exhibited an electrical conductivity of approximately 42 S/cm, surpassing that of cellulose (approximately 15 S/cm). Moreover, the same fibers demonstrated significantly improved tensile strength (∼312 MPa), showcasing a 5-fold increase compared to pure cellulose while maintaining lower stiffness. Comprehensive analyses, including Auger electron spectroscopy and wide-angle X-ray scattering, show a heterogeneous skin-core morphology in the fibers revealing a higher degree of preferred orientation of carbon components in the skin compared to the core. The incorporation of lignin in CFs leads to increased graphitization, enhanced tensile strength, and a unique skin-core structure, where the skin's graphitized cellulose and lignin contribute stiffness, while the predominantly lignin-rich core enhances carbon content, electrical conductivity, and strength.

Extraction and characterization of novel fibers from Tecoma stans Linn bark for use as reinforcement in polymer composites

Embarking on a pioneering investigation, this study unravels the extraordinary qualities of Tecoma stans Fibers (TSFs), freshly harvested from the rachis, establishing them as prospective reinforcements for biocomposites. Delving into their intricate characteristics, TSFs exhibit a unique fusion of physical resilience, with a density of 1.81 ± 0.39 g/cc and a diameter of 234.12 ± 7.63 μm. Complementing their physical prowess, their chemical composition boasts a harmonious blend of cellulose (70.1 ± 9.06 wt%), hemicellulose (13.56 ± 4.29 wt%), lignin (7.62 ± 2.39 wt%), moisture (4.21 ± 1.56 wt%), wax (2.37 ± 0.63 wt%), and ash (1.25 ± 0.36 wt%). In the realm of mechanical strength, TSFs showcase an impressive tensile strength of 639 ± 18.47 MPa, coupled with a robust strain at failure of 1.75 ± 0.13 % and a Young Modulus of 36.51 ± 1.96 GPa. Unveiling their crystalline intricacies, these fibers reveal a microfibril angle of 14.66 ± 0.15°, a crystalline index (CI) of 63.83 %, and a crystallite size (CS) of 9.27 nm. Beyond their mechanical marvels, TSFs exhibit unwavering thermal stability, enduring temperatures up to 297.36 °C, with a Tmax reaching an impressive 392.09 °C.

Effect of bio-ethanol industry-based lignin properties on the chemical and high-temperature properties of bitumen–lignin blends

Effect of bio-ethanol industry-based lignin properties on the chemical and high-temperature properties of bitumen–lignin blends

Lignocellulose reconstituted shape-controllable self-supporting carbonaceous capacitance-anodes with high electron transfer rates for high-performance microbial electrochemical system

Natural biomass is a promising candidate for manufacturing an efficient anode in the microbial electrochemical system (MES) for its abundance and low cost. However, the structure and performance of the electrode highly depend on the biomass species. A simple and sustainable method for creating a self-supporting electrode is proposed by freeze-drying and carbonizing a blend of cellulose, lignin, and hemicellulose. This strategy leads to a cork-like structure and improved mechanical strength of the lignocellulose carbon. A power density of 4780 ± 260 mW m−2 (CLX-800) was achieved, which was the highest record for unmodified lignocellulose-based anodes in the microbial fuel cells. The morphological as lamellar multilayer and rich in hydrophilic functional groups could facilitate the formation of thick electroactive biofilms and enrich Geobacter with the highest abundance of 92.3%. The CLX material is expected to be the ideal electrode for high performance and functionally controllability.

Glycol lignin/MAH-g-PP blends and composites with exceptional mechanical properties for automotive applications

Lightweight plastics and their composites are being increasingly used in automobiles to reduce emissions and costs, but the market demand for fossil fuel-based plastics such as polypropylene (PP) creates several environmental problems such as pollution and waste. Although replacing PP with biomass such as lignin is not a new endeavor, the vast majority of past studies reported reduced mechanical properties as lignin content increases, which limits its application in industry. Herein, blends of maleic anhydride-grafted PP (MAH-g-PP) and softwood-derived glycol lignin (GL) are successfully fabricated via a melt-mixing approach, which boast exceptional mechanical properties and thermal stability. Synergistic performance enhancement is observed when combined with carbon fiber reinforcement, which is elucidated by nanoindentation of the fiber/polymer interface. This work contributes to the development of sustainable automotive structures by efficiently combining biomass and traditional materials.

Facile Fabrication of High-Performance Composite Films Comprising Polyvinyl Alcohol as Matrix and Phenolic Tree Extracts.

Given that tree extracts such as tannin and lignin can be efficiently used as modifying materials, this helps to verify the global trend of energy saving and environment protection. Thus, bio-based biodegradable composite film incorporating tannin and lignin as additives, together with polyvinyl alcohol (PVOH) as a matrix (denoted TLP), was prepared. Its easy preparation process endows it with high industrial value in comparison to some bio-based films with complex preparation process such as cellulose-based films. Furthermore, imaging with scanning electron microscopy (SEM) shows that the surface of tannin- and lignin-modified polyvinyl alcohol film was smooth, free of pores or cracks. Moreover, the addition of lignin and tannin improved the tensile strength of the film, which reached 31.3 MPa as indicated by mechanical characterization. This was accounted for by using Fourier transform infrared (FTIR) and electrospray ionization mass (ESI-MS) spectroscopy, which showed that the physical blending of lignin and tannin with PVOH was accompanied by chemical interactions that gave rise to weakening of the prevailing hydrogen bonding in PVOH film. In consequence, the addition of tannin and lignin acquired the composite film good resistance against the light in the ultraviolet and visible range (UV-VL). Furthermore, the film exhibited biodegradability with a mass loss about 4.22% when contaminated with Penicillium sp. for 12 days.

Processing and characterization of carbon nanofibers obtained from PAN/lignin blends processed by electrospinning

AbstractBlankets based on blends with different PAN/lignin ratios (10 and 50% wt. of lignin) were processed via electrospinning. Then, the blankets obtained were thermally treated in order to produce samples of carbon nanofibers. The thermo‐oxidative stabilization parameters were defined based on a 23‐factorial design. The samples, after stabilization, were analyzed by differential scanning calorimetry (DSC), thermogravimetry (TGA), scanning electron microscopy (SEM), and Fourier transform infrared spectroscopy (FT‐IR) techniques. Based on the results, the best parameters for the stabilization of electrospun, blankets were selected, and subsequently, the most adequate carbonization parameters were established to obtain the carbon blankets. The carbonized blankets were characterized for electrical conductivity by impedance spectroscopy, chemical structure (Raman and FT‐IR spectroscopies), crystallographic ordering by X‐ray diffraction (XRD), and morphology (SEM). The results showed the feasibility of producing carbon blankets based on PAN/lignin blends. However, carbonized blankets showed low carbon yield (10–56%) and a decrease of up to 70% in fiber diameter. XRD and Raman spectroscopy showed that the structural ordering of carbon blankets presents different values according to the heat treatment parameters used (45–57%) and a poorly ordered structure, indicated by the ID/IG ratio.

Enhancement of 3D Printability by FDM and Electrical Conductivity of PLA/MWCNT Filaments Using Lignin as Bio-Dispersant.

To increase the applications of FDM (fusion deposition modeling) 3D printing in electronics, it is necessary to develop new filaments with good electrical properties and suitable processability. In this work, polymer composites filament-shaped with superior electrical performance based on polylactic acid (PLA) carbon nanotubes and lignin blends have been studied by combining solution mixing and melt blending. The results showed that composites achieve electrical percolation from 5 wt.% of nanotubes, with high electrical conductivity. Moreover, the introduction of a plasticizing additive, lignin, improved the printability of the material while increasing its electrical conductivity (from (1.5 ± 0.9)·10-7 S·cm-1 to (1.4 ± 0.9)·10-1 S cm-1 with 5 wt.% carbon nanotubes and 1 wt.% lignin) maintaining the mechanical properties of composite without additive. To validate lignin performance, its effect on PLA/MWCNT was compare with polyethylene glycol. PEG is a well-known commercial additive, and its use as dispersant and plasticizer in PLA/MWCNT composites has been proven in bibliography. PLA/MWCNT composites display easier processability by 3D printing and more adhesion between the printed layers with lignin than with PEG. In addition, the polyethylene glycol produces a plasticizing effect in the PLA matrix reducing the composite stiffness. Finally, an interactive electronic prototype was 3D printed to assess the printability of the new conducting filaments with 5 wt.% of MWCNT.

Copyrolysis of microalga Chlorella sp. and alkali lignin with potassium carbonate impregnation for synergistic Bisphenol A plasticizer adsorption

Composite functional materials offer promising opportunities for the development of tailored adsorbents with enhanced bioremediation potential towards toxic, carcinogenic endocrine disrupters such as Bisphenol A (BPA). Copyrolysis of microalga Chlorella sp. (CH) alkali lignin (L) with K2CO3 impregnation yielded a carbon-based composite (CHL-AC) with a micro–mesoporous structure of 0.643 cm3/g, surface area of 1414 m2/g, and BPA adsorption capacity of Qmax 316.858 mg/g. Enhanced BPA removal efficiency indicated a positive synergistic effect upon a combination of L and CH, resulting in a 73.24 % removal efficiency compared with the individual carbon components of 52.33 % for L-AC and 67.35 % for CH-AC. The kinetics and equilibrium results were described well by the pseudo second-order kinetic model and Freundlich isotherm, respectively. This paper elucidates the blending of microalgae and lignin into high-value carbon composite material, CHL-AC, with immense potential for the treatment of BPA-contaminated waters to contribute to Goal 6 (clean water and sanitation).

Valorization of Kraft Lignin from Black Liquor in the Production of Composite Materials with Poly(caprolactone) and Natural Stone Groundwood Fibers

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

Variation in the hierarchical structure of lignin-blended cellulose precursor fibers

Regenerated cellulose fibers have been considered as potential precursor fibers for carbon fibers because of their balanced cost and performance. Increased attention has been paid to blending lignin with the regenerated cellulose to generate precursor fibers which render good mechanical properties and higher carbon yield. The mechanical properties of carbon fibers have been found closely correlated to the structure of precursor fibers. However, the effects of lignin blending on molecular- and morphological structure of the precursor are still unclear. This study aims at clarifying the structural information of lignin–cellulose precursor fibers from molecular level to mesoscale by scanning X-ray microdiffraction. We present the existence of a skin–core morphology for all the precursor fibers. Increase of lignin content in precursor fiber could reduce the portion of skin and cause obvious disorder of the meso- and molecular structure. By correlating structural variations with lignin blending, 30% lignin blending has been found as a potential balance point to obtain precursor fibers maintaining structural order together with high yield rate.

Economic and competitive potential of lignin-based thermoplastics using a multicriteria decision-making method

As a result of new lignin extraction plants hatching and increasing volumes of technical lignin becoming available, a variety of lignin derivatives, including phenolic resins and polyurethane (PU) foams, are reaching the marketplace or being used as intermediate products in many industrial applications. In the spectrum of possible lignin derivatives, thermoplastics appear particularly attractive due to a symbiosis of market, policy, and technology drivers. To assess the preferredness for lignin-based thermoplastics, this paper adapted a risk-oriented methodology formerly applied to assess lignin usage in various applications (phenol-formaldehyde [PF] resins, PU foams, and carbon fiber applications) to the case of lignin-based thermoplastics using hydroxypropylated lignin (HPL) and miscible blends of lignin and polyethylene oxide (PEO). The HPL is considered for garbage bags and agricultural films applications, while lignin-PEO blends are used as replacement for acrylonitrile butadiene styrene (ABS) in applications such as automotive parts. In the methodology, two phased-implementation strategies were defined for each thermoplastic derivative, considering perspectives for profit maximization (90 metric tons/day integrated units) and revenue growth (350 metric tons/day overall capacity), which were considered for implementation within a softwood kraft pulping mill. A set of six criteria representative of the main economic and market competitiveness issues were employed, and their respective importance weights were obtained in a multicriteria decision-making (MCDM) panel. Early-stage techno-economic estimates were done as a basis for the calculation of decision criteria. Compared to product derivatives previously assessed, capital investment for thermoplastic strategies appeared marginally higher due to the required lignin modification steps (on average 30% higher at similar capacity, and 6% for higher-scale revenue diversification strategies). Higher operating costs were also observed due to increased chemical expenses for all thermoplastic strategies, which are ultimately balanced by revenues associated with targeted thermoplastic products, leading to greater annual margins and cash flow generation over the project lifetime for thermoplastic strategies compared to other product applications (58% to 66% higher on average, at similar scale). Benefits of improved economics were reflected in economic criteria, internal rate of return (IRR), and cash flow on capital employed (CFCE), as well as in the price competitiveness criterion, CPC. Overall, the combination of relatively high lignin content in the plastic formulation and the less costly modification method contributed to lignin-PEO strategies, gaining the top two rankings. Based on their overall scores, both strategies defined for HPL would also integrate the group of “preferred” strategies, but are outranked by strategies that consider lignin positioning on PU foam applications.

Investigation of the Characteristic Properties of Lignin-Modified Bitumen

The main objective of this study was to investigate the characteristic properties of lignin-modified bitumen with different lignin contents. The first step was the characterization of the physicochemical and thermal properties of the kraft lignin powder along with the determination of its microstructure. This was achieved by carrying out an elemental analysis, Gel Permeation Chromatography (GPC), Thermogravimetric Analysis (TGA)/Derivative Thermogravimetry (DTG), Fourier Transformation Infrared (FTIR) spectroscopy, Scanning Electron Microscopy (SEM), Dynamic Light Scattering (DLS) and Confocal Microscopy. After the latter tests, three (3) blends with different lignin contents (5%, 10% and 15% by weight of bitumen) were produced. Characteristic properties such as penetration, softening point, elastic recovery, force ductility, dynamic viscosity and storage stability were determined for the reference bitumen and the three lignin blends. The main conclusion was that kraft lignin powder hardens the conventional bitumen. Specifically, the addition of 15% lignin to the bitumen hardened the blend to such a degree that the bitumen changed category from 50/70 to 35/50 with respect to EN 12591.

Uniformly Dispersed Poly(lactic acid)-Grafted Lignin Nanoparticles Enhance Antioxidant Activity and UV-Barrier Properties of Poly(lactic acid) Packaging Films.

Poly(lactic acid) (PLA) represents one of the most widely used biodegradable polymers for food packaging applications. While this material provides many advantages, it is characterized by limited antioxidant and UV-barrier properties. Blending PLA with lignin is an attractive strategy to address these limitations. Lignin possesses antioxidant properties and absorbs UV-light and is a widely available low value byproduct of the paper and pulp industry. This study has explored the use of lignin nanoparticles to augment the properties of PLA-based films. A central challenge in the preparation of PLA–lignin nanoparticle blend films is to avoid nanoparticle aggregation, which could compromise optical properties as well as antioxidant activity, among others. To avoid nanoparticle aggregation in the PLA matrix, PLA-grafted lignin nanoparticles were prepared via organocatalyzed lactide ring-opening polymerization. In contrast to lignin and unmodified lignin nanoparticles, these PLA-grafted lignin nanoparticles could be uniformly dispersed in PLA for lignin contents up to 10 wt %. The addition of as little as the equivalent of 1 wt % of lignin of these nanoparticles effectively blocked transmission of 280 nm UV-light. At the same time, these blend films retained reasonable visible light transmittance. The optical properties of the PLA lignin blend films also benefited from the well-dispersed nature of the PLA-grafted nanoparticles, as evidenced by significantly higher visible light transmittance of blends of PLA and PLA-grafted nanoparticles, as compared to blends prepared from PLA with lignin or unmodified lignin nanoparticles. Finally, blending PLA with PLA-grafted lignin nanoparticles greatly augments the antioxidant activity of these films.

Investigating the Effects of Tobacco Lignin on Polypropylene.

The utilization of eco-friendly materials, such as lignin, for higher value product applications became increasingly important as environmental concerns due to global warming increased. Melt blending is one of the easy ways to increase the usage of lignin in commercial applications. However, the degradation of the final product performance and increase in the production time and costs are of major concern. In the current work, the effects of blending lignin, extracted from tobacco plants, with polypropylene (PP) on the injection molding parameters, physical, thermal and mechanical properties are investigated. Blends of lignin (5, 15 and 30% by wt.) with PP were prepared using a Filabot single screw extruder. Results show that tensile strength decreases by 3.2%, 9.9% and 5.4% at 5 wt. %, 15 wt. %, and 30 wt. % of lignin addition, respectively. The tensile stiffness was almost unaffected by the addition of up to 15% lignin, but a 23% increase was observed at 30 wt. % loading. When compared to lignin processed via expensive processes, such as acetylation, tobacco lignin showed superior performance. The DSC results show unaffected crystallization and melting temperatures but a decrease in enthalpies and percentage of crystallinity. The SEM and optical micrographs of the coupon cross-sections show that the extrusion process has achieved a uniform distribution of lignin particles in the PP. Thermogravimetric analysis results show that tobacco lignin accelerates the onset decomposition temperature but does not influence the decomposition peak temperature. The increase in lignin content did not have a significant influence on the injection molding parameters, implying no additional processing costs for adding lignin to the PP. Overall, the performance of the tobacco lignin is comparable, if not better, than that of processed lignin reported in the literature.

Odor and Constituent Odorants of HDPE-Lignin Blends of Different Lignin Origin.

The still-rising global demand for plastics warrants the substitution of non-renewable mineral oil-based resources with natural products as a decisive step towards sustainability. Lignin is one of the most abundant natural polymers and represents an ideal but hitherto highly underutilized raw material to replace petroleum-based resources. In particular, the use of lignin composites, especially polyolefin–lignin blends, is currently on the rise. In addition to specific mechanical property requirements, a challenge of implementing these alternative polymers is their heavy odor load. This is especially relevant for lignin, which exhibits an intrinsic odor that limits its use as an ingredient in blends intended for high quality applications. The present study addressed this issue by undertaking a systematic evaluation of the odor properties and constituent odorants of commercially available lignins and related high-density polyethylene (HDPE) blends. The potent odors of the investigated samples could be attributed to the presence of 71 individual odorous constituents that originated primarily from the structurally complex lignin. The majority of them was assignable to six main substance classes: carboxylic acids, aldehydes, phenols, furan compounds, alkylated 2-cyclopenten-1-ones, and sulfur compounds. The odors were strongly related to both the lignin raw materials and the different processes of their extraction, while the production of the blends had a lower but also significant influence. Especially the investigated soda lignin with hay- and honey-like odors was highly different in its odorant composition compared to lignins resulting from the sulfurous kraft process predominantly characterized by smoky and burnt odors. These observations highlight the importance of sufficient purification of the lignin raw material and the need for odor abatement procedures during the compounding process. The molecular elucidation of the odorants causing the strong odor represents an important procedure to develop odor reduction strategies.

Influence of the carbonization temperature on the properties of carbon fibers based on technical softwood kraft lignin blends

Lignin is an interesting renewable resource for carbon fibers. In this work we investigate the usage of unpurified softwood kraft lignin Indulin AT for melt-spinning of lignin-fibers and the properties of resulting lignin and carbon fibers. Indulin AT is blended with 10, 15 and 20 wt% polyethylene glycol (PEG) and melt-spun on a pilot plant. The obtained as-spun lignin fibers are stabilized in air and afterwards transformed to carbon fibers at carbonization temperatures of 900 °C, 1500 °C, 2000 °C and 2300 °C. Along the process chain the fibers are characterized by mechanical testing, scanning electron microscopy, X-ray diffraction (XRD) and Raman spectroscopy to provide insight into the structure and quality of the lignin and carbon fibers. Additionally, analytical studies show strong intermolecular interactions between Indulin AT and polyethylene glycol. Despite the high ash content the resulting carbon fibers exhibit promising mechanical properties. XRD and Raman show the increase in ordered carbon structures with an increasing carbonization temperature. Blends of unpurified Indulin AT and PEG are successfully used for melt-spinning of lignin fibers and production of low-cost carbon fibers thereof.

Slow release fertilizer prepared with lignin and poly(vinyl acetate) bioblend

Controlled or slow release fertilizers have been recommended to enhance crop yield, while minimizing environmental and economic issues related from current fertilizer applications. However, alternative biodegradable and non-toxic coating material should be suggested to produce biocoated fertilizers. Here we propose the use of lignin and poly(vinyl acetate) (PVAc) as biocoating materials for preparing slow release urea fertilizer. The blend of PVAc and lignin at a mass ratio of 75:25 improved the characteristics of the formed film and increased the nitrogen release time if compared to the pure polymers. The nitrogen release time from urea granules coated with a polymeric layer of 154.3 ± 5.5 μm formed by lignin and PVAc was 36 times greater than from bare urea. The increase in the polymeric coating from 52.6 ± 5.2 to 80.2 ± 6.1 μm decreased the curvature of the nitrogen release data by a factor of at least 1.7, while the curvature was decreased in at least 1.3 with the increase in the polymeric coating from 80.2 ± 6.1 to 158.9 ± 10.6 μm. The adjustment of nitrogen release data to the Peppas-Sahlin model indicated the Fickian diffusion is more predominant than relaxation contributions, since the used polymers did not present considerable swelling. Thus, the blending of PVAc and lignin at 25 wt% of lignin and 75 wt% of PVAc is suggested as a biocoating material for producing slow release fertilizers.

Preparation of polypropylene with high melt strength by wet reaction blending of lignin

AbstractIn this paper, the melt strength of polypropylene is shown to be significantly improved by lignin‐cooperative construction of heterophase network structure and the evolution mechanism of lignin on the topology of polypropylene is investigated. Electron paramagnetic resonance (EPR) analysis shows that the free radicals generated by polypropylene irradiation can remain active for 2 weeks; rheological studies show that lignin promotes the formation of heterogeneous network structures in polypropylene, and its melt is characterized by long‐chain branching. Phase angle‐complex modulus, complex viscosity‐complex modulus, Han's, and Cole–Cole curves are used to analyze the liquid–solid transformation, and the results indicate that the enhanced interfacial action is due to the formation of the heterogeneous network structures. The mechanical properties show that the impact strength is increased by 1.8 times due to the synergistic effect of lignin and acrylamide. SEM shows the formation of a fibrous network structure around the lignin, which undergoes interfacial yielding, improving the interfacial interaction between the components.