Enhanced Flame Retardancy Research Articles

Multifunctional-structural integrated wood cellulose‑based composite with Magpie’s Nest-shaped enhance flame retardancy and electromagnetic interference shielding

The construction of multifunctional hydrophobic wood with electromagnetic interference shielding effectiveness had attracted great interest, at the same time, the problem of wood flammability must also be solved. In this study, the effectiveness of DOPO-based P and Zn complexes in improving wood flame retardancy and electromagnetic interference shielding effectiveness, and the outstanding contribution of lignocellulose skeleton and multi-interface to shielding effectiveness was demonstrated. DOPO-based P and Zn complexes with “Needle-punched” structure and much functional groups were loaded on the wood surface, and then micro-nano metal Ni particles were deposited. Through the optimization of the wood surface and itself structure, and the construction of a complete conductive network. Wood/ZnP/Ni composites electromagnetic interference shielding effectiveness couold reach 65.04 dB in the X-band. It was worth noting that the lignocellulose skeleton prepared by the top-down method and multi-interface structure increase electromagnetic interference shielding effectiveness by 10.71 % and 33.89 %, respectively. In addition, the synergistic effect of DOPO-based P and Zn complexes and the introduction of PDMS layer improved the flame retardancy (limiting oxygen index was 35.3 %) and hydrophobicity (contact angle was 133.07°), which avoided the wood poor durability problem in use. There was no doubt that it provided a new strategy for the preparation of novel materials with low-cost and extremely excellent electromagnetic interference shielding properties.

Enhancing flame retardancy of flexible polyurethane foams through one-step coassembled nanocoatings

Enhancing flame retardancy of flexible polyurethane foams through one-step coassembled nanocoatings

Enhancing mechanical durability and flame retardancy in Bamboo-Polypropylene composites with nAl2O3 fillers

Enhancing mechanical durability and flame retardancy in Bamboo-Polypropylene composites with nAl2O3 fillers

Enhanced flame retardancy and mechanical properties of poly (lactic acid) composites via piperazine pyrophosphate and nanoscale cerium dioxide synergistic flame retarding and uniaxial pre-stretching

The simultaneous improvement of flame retardancy and mechanical properties (including strength, rigidity, and toughness) of PLA was achieved for the first time. A synergistic flame retardant system including PAPP and nano-CeO2 was used to enhance the flame retardant properties of PLA. Especially, uniaxial pre-stretching was further used to improve the mechanical properties of the flame-retardant PLA composites. With the addition of just 1 wt% nano-CeO2, the flame retardant properties of PLA composite were significantly enhanced. Relative to pure PLA, the limiting oxygen index (LOI) of PLA/14 wt%PAPP/1 wt% nano-CeO2 increased from 20.2 % to 28.8 %, achieving a V-0 rating in the UL-94 test. Moreover, the peak heat release rate (PHRR) was reduced from 461KW/m2 to 230KW/m2. Notably, the flame-retardant PLA composites with excellent mechanical properties were achieved using uniaxial pre-stretching for the first time. After pre-stretching, the tensile strength, elongation at break and impact strength of the flame-retardant PLA were significantly increased to 79.82 MPa, 103.8 %, and 9.7 kJ/m2, respectively. This work proposes an ingenious strategy for significantly enhancing both the fire safety and mechanical properties of PLA composites.

Hierarchical Nano/Micro-Array Structured CuMgAl-LDH/rGO Hybrids for Remarkably Improved Flame Retardancy and Smoke Suppression Performance of Flexible Polyvinyl Chloride.

In this study, we explored the rational integration of layered double hydroxides (LDHs) with reduced graphene oxide (rGO) to create a hierarchical nano/microarray structured CuMgAl-LDH/rGO hybrid aimed at enhancing the flame retardancy and smoke suppression properties of polymer nanocomposites. The results indicated that the limiting oxygen index (LOI) value of the G-CuMgAl/polyvinyl chloride (PVC) composite reached 35.8%, reflecting a 6.4% increase compared to pristine PVC (29.4%), and achieved a UL-94 V-0 rating. Furthermore, in comparison to pristine PVC, the peak heat release rate (PHRR) of the G-CuMgAl/PVC composite was significantly reduced by 40.2%; the total heat release rate (THR) decreased by 24.3%; the maximum average heat release rate (MARHE) diminished by 41.6%; the peak smoke production (PSPR) decreased by 37.8%; the total smoke production (TSP) was reduced by 31.3%; and the average effective heat of combustion (av-EHC) decreased by 15.2%. The enhanced flame retardancy and reduced smoke production can primarily be attributed to the multiple synergistic interactions among the highly dispersed constituents and the nano/microstructures, which effectively impede the transfer of heat, mass, and O2 from various directions while preventing further combustion of the underlying matrix by creating a tortuous path in the condensed phase. Additionally, this study provides a novel perspective on the design and synthesis of structured LDHs/rGO hybrids, with the potential to enhance flame retardancy and smoke suppression properties across a broad spectrum of polymer materials.

Construction of epoxy resin with enhanced flame retardancy, mechanical properties, and satisfactory transparency based on a novel bi‐DOPO and hydrogen‐bonding network

AbstractEstablishment of high‐performance epoxy resin with satisfactory fire safety, mechanical properties, and excellent transparency is urgently desirable, but still remains significant challenges. Herein, a super‐tough yet high flame retardant epoxy resin (EP/BTD) was designed and prepared by incorporating bi‐DOPO structure and hydrogen‐bonding networks. Although the phosphorus content was only 0.69 wt% (10 wt% of bi‐DOPO flame retardant [BTD]), EP/BTD‐10 showed a high limiting oxygen index value (33.4%), satisfactory UL‐94 rating (V‐0), and good heat suppression ability (total heat release [THR] and peak heat release rate [PHRR] reduced to 29.0% and 42.2%, respectively). Furthermore, the flame retardant mechanism of EP/BTD was illustrated and attributed to dual‐phase fire‐retardant effect. Additionally, EP/BTD‐7.5 featured notably mechanical properties, of which the tensile strength, elongation at break and impact strength increased by 44.6%, 40.0%, and 232.6%, respectively, due to hydrogen‐bonding network and π–π interaction. More importantly, EP/BTD maintained high visible light transmittance and excellent UV‐blocking properties. In summary, this work provided a guidance for the development of high‐performance epoxy resin and was expected to expand the practical applications.

Enhancing Flame Retardancy in Epoxy Resin with Clever Self-Assembly Method for Optimizing Interface Interaction via Well-Dispersed Cerium Oxide on Piperazine Pyrophosphate

Developing flame-retardant epoxy resins (EPs) is essential to broaden their industrial applications, as their inherent flammability restricts their widespread use. In this study, commercial cerium oxide (CeO2) nanoparticles were modified with oleic acid and successfully assembled onto the surface of pyrophosphate piperazine (PAPP) through a simple solvophobic effect, constructing an integrated superstructure flame retardant, CeO2@PAPP, with enhanced performance integration. Compared to traditional simple blends, the EP composite with 10 wt% CeO2@PAPP displayed superior flame retardancy, thanks to the more subtle synergistic effects between flame retardant components and their favorable interface interactions. The EP composite achieved a UL-94 V-0 rating and increased the limiting oxygen index (LOI) to 34.2%. Significant reductions of 56.3% in peak heat release rate (PHRR) and 38.2% in total heat release (THR) were observed. Furthermore, total smoke release (TSR), carbon monoxide yield (COPR), and carbon dioxide yield (CO2PR) decreased by 52.2%, 50.2%, and 67.3%, respectively. Through comprehensive and detailed characterization, it was discovered that the assembled integrated CeO2@PAPP flame retardant can perform better in both the gas phase and condensed phase, resulting in superior flame-retardant properties. This study offers an effective strategy for developing highly flame-retardant EPs, thereby expanding their potential applications across various industries.

Catalyst-free sustainable epoxy vitrimers with fire safety offered by phosphorus-containing compounds

In this study, we designed and incorporated a phosphorus-rich compound, DPT, which possesses inherent catalytic properties, into a typically sustainable epoxy vitrimer. This innovative strategy enables the fabrication of flame retarded epoxy vitrimers that require no additional catalysts. DPT was synthesized through a reaction between triethanolamine (TEA) and dibenzyl chlorophosphonate (DPCP). The successful synthesis of DPT is attested to by FTIR and NMR analyses. DPT effectively accelerated the curing process of the epoxy vitrimers, yielding materials with exceptional mechanical strength and inherent self-healing abilities. Notably, the pHRR of epoxy vitrimer incorporated with DPT is reduced to 296.3 kW/m2, showing a remarkable 54% reduction compared to that of the epoxy vitrimer catalyzed by conventional catalysts. The THR is also decreased from 84.3 to 42.4 MJ/m2. Comprehensive analyses using cone calorimetry and TG-FTIR revealed that DPT effectively inhibits the emission of toxic gases. Crucially, the presence of DPT in the epoxy matrix facilitated the formation of a dense and stable phosphorus-laden carbon layer, which not only enhanced flame retardancy but also imparted exceptional smoke suppression capabilities. These findings underscore the potential of DPT for developing high-performance, catalyst-free, flame-retardant epoxy vitrimers.

Double cross-linked biomass aerogels with enhanced mechanical strength and flame retardancy for construction thermal insulation

Biomass aerogels are expected to be a popular material in construction field due to their sustainability, eco-friendliness and excellent thermal insulation properties. In this paper, high modulus biomass aerogels based on the principle of double cross-linking of physics and chemistry were synthesized by freeze-drying technique using gelatin, sodium carboxymethyl cellulose, glutaraldehyde, phytic acid and diatomite as raw materials. The presence of a double cross-linked network structure endowed the prepared aerogels with a low thermal conductivity (0.021–0.029 W·m−1·k−1). The density of only 0.0865 g·cm−3 biomass aerogel exhibited an extrastrong compression modulus of 31.5 MPa, which was superior to common biomass aerogels. Biomass intumescent flame retardant system composed of sodium carboxymethyl cellulose (carbon source), gelatin (gas source) and phytic acid (acid source) was used in combination with diatomite to enhance flame retardancy (limit oxygen index value up to 36.5 %, UL-94 V-0 rating and total smoke production reduced from 0.31 m2 to 0.18 m2) and thermal stability (the residue up to 48.91 %). Remarkably, the modified aerogel showed incredible hydrophobicity (hydrophobic angle of 137°). In summary, the results indicated this study proposed a novel green idea for the preparation of construction thermal insulation materials with a combination of high modulus, flame retardancy and hydrophobicity.

Synchronously enhanced flame retardancy and mechanical properties of polylactic acid via in-situ assembly of polyphosphazene nanoparticles on ammonium polyphosphate

Polylactic acid (PLA) exhibits wide potential applications in many fields ranging from textile, packaging material to biomedical devices. However, the relatively low mechanical properties and inflammability are obstacles to the expansion of its application. Here, a kind of polyphosphazene nanoparticles with tannic acid (TA) as template, hexachlorocyclotriphosphazene (HCCP) and 4,4′-Sulfonyldiphenol (BPS) as comonomers were prepared (named as HTB), and then combined with ammonium polyphosphate (APP) to enhance the comprehensive properties of PLA composites. The introduction of HTB strengthened the interfacial adhesion of composites via constructing the hydrogen bond interaction between PLA and APP, promoting the homogenous dispersion of APP in the composite and the formation of APP network. The flame retardant measurements presented that incorporating 10 wt% APP and 5 wt% HTB in PLA increased the limit oxygen index (LOI) value to 31.0% and endowed the composite with the V-0 rating of UL-94 test and simultaneously, the peak of heat release rate (PHRR) and total heat release (THR) of the composite decreased by 14.2% and 13.2% compared with pure PLA. Specially, there was almost no melt drip appeared during the combustion process, which was distinctly different from the combustion behavior of the composite containing only 20 wt% APP with the V-2 rating of UL-94 test. The uniform dispersion of APP in the PLA matrix and the strong interfacial adhesion between APP and the PLA matrix contribute to the enhancement of the mechanical properties of composites, and the elongation at break, Young’s modulus and impact strength of the composite were increased by 52.9%, 7.6% and 24.2%, respectively. The present study offers novel insights for the trade-off between flame retardancy and mechanical properties with PLA composites.

MOF-derived strategy for in-situ assembly of nickel phyllosilicate nanoflowers: Enhancing smoke suppression, flame retardancy and mechanical properties of epoxy resins

Epoxy resin (EP) is a highly versatile polymer extensively used in high-end applications, including aerospace components, electronics encapsulation and adhesives. To custom-design flame retardant materials for high-performance epoxy resins, a MOF-derived zeolitic imidazolate framework-8@nickel phyllosilicate (ZIF@Ni-PS) was synthesized through the in-situ assembly of nickel phyllosilicate nanoflowers. The results showed that the smoke suppression, flame retardancy, and mechanical properties of the EP composites containing 5 wt% ZIF@Ni-PS were significantly enhanced. The peak heat release rate (pHRR) and the peak smoke production rate (pSPR) were reduced by 33.2% and 12.7%, respectively. The presence of ZIF@Ni-PS promoted the formation of a dense, high-quality carbon layer that isolated heat and oxygen transfer, effectively reducing heat release during combustion and suppressing smoke generation. Furthermore, the imidazole ring and Zn ions on the surface of ZIF@Ni-PS facilitated the formation of coordination and hydrogen bonds with the epoxy (EP), thereby enhancing the dispersion, compatibility, and mechanical properties of the epoxy resin matrix. This study presents a straightforward preparation method for high-performance EP composites, providing a novel pathway for EP research.

Enhancing flame retardancy and mechanical strength of glass fiber-reinforced biomass polyamide composites with surface-functionalized black phosphorus

Fiber-reinforced polyamide exhibits exceptional mechanical properties and durability; however, its widespread application is impeded by potential fire hazards. In this study, a hybrid material consisting of black phosphorus (BP) and polyhedral oligomeric silsesquioxane (POSS) was synthesized, denoted as BP-CO-POSS. The fire safety of fiber-reinforced polyamide demonstrated significant enhancement upon the incorporation of aluminum diethyl phosphinate (Alpi) and BP-CO-POSS. This enhancement was evident in various aspects, including the suppression of heat release behaviors, reduction in the emission of toxic gases, and an increase in the UL-94 rating. Notably, with the additional inclusion of 0.5 wt% BP-CO-POSS, a substantial decrease in both heat release rate (31.15 %) and total heat release (37.59 %) was observed when compared to the application of Alpi and BP alone, thus affirming the existence of a synergistic effect. This observation was substantiated through a comprehensive analysis of results obtained from both gas and condensed phases. This study offers a practical methodology for the widespread utilization of phosphorus-rich advanced materials, thereby further enhancing the fire safety of fiber-reinforced polymers.

Biomass Hydrogel Electrolytes toward Green and Durable Supercapacitors: Enhancing Flame Retardancy, Low-Temperature Self-Healing, Self-Adhesion, and Long-Term Cycling Stability.

Hydrogels have shown promise as quasi-solid-state electrolytes for flexible supercapacitors but face challenges such as poor self-repair, unstable electrode adhesion, limited temperature range, and flammability. Herein, an all-round green hydrogel electrolyte (silk nanofibers (SNFs)/peach gum polysaccharide (PGP)/borax/glycerol (SPBG)-ZnSO4) addresses these issues through dynamic cross-linking of peach gum polysaccharide and silk nanofibers with borax, integrating varieties of key property including high water retention, broad temperature tolerance (-20 to 90 °C), excellent self-adhesion (60.7 kPa for carbon cloth electrodes), satisfactory flame retardancy (limited oxygen index of 51%), low-temperature self-healing (-20 °C), and good ionic conductivity (7.68 mS cm-1). The resulting supercapacitor exhibits excellent cycling stability with 98.2% capacitance retention after 40,000 long cycles at 25 °C. The specific capacitance retention remains above 90% even after 15,000 cycles at high/low temperatures (50 °C/-20 °C). Furthermore, the flexible supercapacitor demonstrates stable performance under mechanical stimuli (180° bending and perforation), highlighting the potential of biomass hydrogels in flexible energy storage devices.

Pyrolysis kinetics and flame retardant enhancement of bio-based polyamide 56/6

The development of polyamide materials with fire safety is of great importance at this stage. A novel nitrogen-phosphorus bisystem flame retardant (MC) with a multi-branched structure was synthesized and applied to a new bio-based polyamide 56/6 (PA56/6). Notably, at 8 wt% MC content, flame-retardant PA56/6@MC8% (FRPA56/6@MC8%) achieved an Limiting Oxygen Index (LOI) of 26.6% and a V-0 rating in UL-94 tests. Cone calorimetry results indicated that FRPA56/6@MC8% exhibited a 22.9% reduction in total heat release (THR) and a 41.0% decrease in peak heat release rate (PHRR), underscoring the flame retardancy promotion by MC in PA56/6. The study further explored the pyrolysis kinetics and mechanisms of polyamide materials, offering insights crucial for flame-retardant modifications. Overall, the findings present an innovative strategy for enhancing the flame retardant properties of PA56/6, potentially applicable in automotive components and other pertinent fields.

Enhancing flame retardancy in 3D printed polyamide composites using directionally arranged recycled carbon fiber

Combining recycled carbon fiber (rCF) and 3D printing technology has shown great potential for fabricating functional prototypes and production parts used in the aerospace and automotive industries. However, it is still a challenge to design flame-retardant 3D printed parts with high mechanical properties and flame-retardant rating. In the work, a flame-retardant polyamide (PA)-based composite for material extrusion 3D printing was prepared by utilization of rCF, polyhedral oligomeric silsesquioxanes (POSS), and 9,10-Dihydro-9-oxa-10-phosphaphenanthrene (DOPO)-based flame retardant. The 3D-printed composites have high thermal stability, mechanical properties, and excellent flame retardancy with a V-0 rating. With the benefits of material extrusion 3D printing, directionally arranged rCF in 3D printed composites could effectively inhibit the fire spread, extend the time to ignition (TTI), reduce the total heat release (THR) and total smoke release (TSR) of 3D printed composites. The directional flame-retardant mechanism is mainly the thermal conductivity mechanism of the condensed phase and the promotion of stable ordered carbon layer formation. It provides a promising path for designing high-performance flame-retardant materials.

Advanced flame-retardant melamine foam with ultra-sensitivity and prolonged fire warning, featuring smart device-integrated graphene oxide/attapulgite nano-coating

Enhancing flame retardancy and fire-warning capabilities of thermal insulation materials used in building external walls is crucial for ensuring fire safety as well as guarding people's lives and assets. Herein, we have developed an environmentally friendly nano-coating that possesses flame-retardant and early-warning properties by integrating graphene oxide (GO) and attapulgite (ATP) onto melamine foam (MF) through a layer-by-layer self-assembly method (LBL). The GO-ATP-MF composite demonstrates a rapid response to flame (<1 s) due to GO's thermally induced reduction. Additionally, ATP's synergistic flame-retardant effects on both gas and condensed phases contribute to outstanding flame retardancy, enabling an enduring fire alarm duration (>1330 s). The warning duration time of this composite surpasses the majority of GO-based fire-warning nano-coatings reported to date. Moreover, incorporating a Bluetooth wireless transmission system facilitates real-time fire information sharing among smart devices, thereby optimizing fire signal transmission efficiency. Thus, this study advances GO-based flame-retardant nano-coatings and devices with high sensitivity and prolonged fire-warning capabilities, providing an innovative idea to enhance the fire safety of MF as a thermal insulation material.

Enhanced flame retardancy and thermal insulation of epoxy resins composites incorporated with ammonium polyphosphate and ionic liquids loaded CuO-ZnO hollow spheres

Epoxy resin, as a thermosetting polymer material with good performance, has been limited in application due to its high flammability. In this investigation, porous CuO-ZnO hollow spheres (CZHS) were prepared by a hydrothermal method. By incorporation with ionic liquids loaded CuO-ZnO hollow spheres (CZHS@Ils) and ammonium polyphosphate (APP) into epoxy resin (EP) matrix, a new composite flame retardant material, named as EP/7.5APP/1.5CZHS@ILs, was developed for improvement of their thermal insulation and flame retardancy. The thermal conductivity of EP/7.5APP/1.5CZHS@ILs was measured to be 0.0197 W m −1 K −1, which is lesser than that of APP incorporated epoxy resin (EP/APP), demonstrating good thermal insulation capability. The flame retardancy were assessed using the limiting oxygen index (LOI) test, the Vertical flame testing (UL-94) test, and the cone calorimeter (CC) test. The results obtained from LOI test show that the EP/7.5APP/1.5CZHS@ILs has good flame retardancy with a LOI value of up to 28, better than that of pure EP which has a LOI value of 19.2. Moreover, a V-0 level of the EP/7.5APP/1.5CZHS@ILs was observed from the UL-94 test. The peak heat release rate (PHRR) was reduced to 257.9 kW m−2, which is 74.8 % lower than that of the pure EP. Such results are attributed to the synergy effect of CZHS@ILs and APP which offers the epoxy resin excellent flame retardancy. Taking advantages of the excellent thermal insulation, flame retardancy and better mechanical properties, the as-resulted EP/7.5APP/1.5CZHS@ILs may hold great potential for future thermal insulation and flame-retardant applications of energy saving building.

Construction of a β-cyclodextrin-based colloid containing silicon, phosphorus and nitrogen components: Toward enhancing flame retardancy of flax fabrics

Natural cellulose fabrics, as one of the combustibles prone to causing indoor fires, are modified with flame retardants encouraged by the fire protection industry. Herein, a bio-based colloid named ASDPC was prepared by 3-aminopropyltriethoxysilane, diethylenetriaminepentakis(methylphosphonic acid) and β-cyclodextrin, and used to enhance the flame retardancy of flax fabrics via the pad-dry-cure method. The treated flax fabrics named ASDPC-FF showed good flame retardancy with a damaged length of only 6.4 cm in the vertical burning test and a limiting oxygen index value of up to 33.8 %. Meanwhile, ASDPC-FF exhibited thermal stability and combustion behavior distinct from untreated flax fabrics. Thermogravimetric analysis presented that the char residue produced by ASDPC-FF at 800 °C was as high as 36.2 %. Cone calorimetry test indicated that the peak heat release rate and total heat release of ASDPC-FF decreased by approximately 89.0 % and 35.7 %, respectively. Furthermore, compared to untreated flax fabrics, condensed-phase and gas-phase studies found that ASDPC-FF turned into expanded char and produced fewer gaseous volatiles containing C-H, CO and C-O-C at high temperatures. More importantly, ASDPC-FF remained self-extinguishing after 25 laundering cycles with flame retardancy surpassing untreated flax fabrics. In summary, this work provides a novel route for expanding the manufacture of flame-retardant flax fabrics.

In situ preparation of MoS2@Fe3O4 by radiation method and its application in flame retardancy, mechanical properties, and friction properties of EVA composites

In recent years, there has been significant interest in using two-dimensional MoS2 to enhance flame retardancy, which has proven challenging. MoS2@Fe3O4 nanosheets were successfully synthesized via a one-step method called radiation reduction to boost MoS2’s flame retardant properties. Incorporating these MoS2@Fe3O4 nanocomposites notably improved the flame retardancy of ethylene vinyl acetate copolymer (EVA). Compared to pure EVA, EVA nanocomposites with 1 part of MoS2@Fe3O4 showed a 17.4% reduction in peak heat release rate, 40.4% decrease in total heat release, and 52.9% reduction in total smoke release, with scaly residue content improving from 0.4% to 12.6%. Additionally, MoS2@Fe3O4 incorporation enhanced the mechanical and friction properties of EVA composites, increasing tensile strength by 25.7% and elongation at break by 10.4% compared to pure EVA. This study presents an effective and simple method for producing modified MoS2 nanosheets that enhance flame retardancy, as well as mechanical and friction properties of EVA composites.

Miscanthus floridulus-based intumescent flame retardant by green self-assembly for fully biological EP composites with commendable flame retardancy, smoke suppression and mechanical properties

The design of fully biological epoxy resin (EP) composites with high performance is highly desirable driven by green and sustainable development due to their renewable and sustainable nature. Herein, an efficient intumescent flame retardant based on Miscanthus floridulus (MF-based IFR) was devised for bio-epoxy composites by a green self-assembly method. The resulting composites with 15 wt% MF-based IFR demonstrated outstanding flame retardancy, effective smoke suppression, and favorable mechanical properties. The enhanced flame retardancy demonstrated the V-0 rating of UL-94 and the 26.4 % of limiting oxygen index (LOI) due to the dual-phase flame-retardant mechanism. Compared to pure EP, the EP composite with 15 wt% MF-based IFR exhibited reductions of 71.90 %, 61.85 %, 55.0 %, and 60.94 % in peak heat release rate (pHRR), total heat release rate (THR), smoke release rate (SPR), and smoke growth rate (TSP), respectively. Additionally, compared to unmodified MF, the composites with 15 wt% MF-based IFR displayed increasing of 3.35 %, 11.26 %, and 10.24 % in tensile, bending, and impact strengths, respectively, attributed to the enhanced interface compatibility. This study provides a straightforward, cost-effective, and efficient strategy for producing fully bio-based epoxy composites with high performance, expanding their potential applications.