Epoxidized Soybean Oil Research Articles

Simultaneous monitoring of epoxy value, hydroxyl value, and polymeric hydroxyl value during the ring opening of epoxidized soybean oils based on low‐field nuclear magnetic resonance coupled with chemometrics

AbstractLow‐field nuclear magnetic resonance technique combined with chemometrics was employed to establish the quantitative models for rapidly monitoring the changes of indicators (hydroxyl value (OHV), epoxy value (EV), polymeric hydroxyl value (POHV, reflecting the degree of polyetherification)) during the ring opening of epoxidized soybean oils. Comprehensively considering the variations of peak retention times and peak areas of LF‐NMR spectra, OHVs of vegetable oils‐based polyols were divided into low OHV (LOHV, 1.7–91.9 mg KOH/g) group and high OHV (HOHV, 94.1–229.4 mg KOH/g) group. In both LOHV and HOHV groups, OHV presented good linearity with T2w, S23, and STotal of relaxation property with correlation coefficient of >0.90. EV and POHV also presented good linearity with relaxation property in both LOHV and HOHV groups. In LOHV group, data segment 1–1000 ms was taken with Deresolve, no preprocessing, and Deresolve as preprocessing methods for OHV, EV, and POHV, respectively, and partial least square (PLS) as the modeling method for all the three indicators, where RMSEPs of OHV, EV, and POHV models were 4.282, 0.114, and 4.061, respectively. In HOHV group, data segment 1–1000 ms was taken with no preprocessing as the preprocessing method and PLS as the modeling method for all the three indicators, where RMSEPs of OHV, EV, and POHV models were 3.117, 0.088, and 4.964, respectively. The established method will benefit polyol industry to online adjust the production parameters according to the monitoring results and achieve high‐quality of vegetable oils‐based polyols.

Sustainable rubber nanocomposites for hydrogen sealings: Impact of carbon nano-onions and bio-based plasticizer

Additives play a crucial role in modifying and enhancing the properties of rubbers, improving mechanical strength, thermal stability, and chemical resistance to make them more suitable for various applications. The rubber industry faces challenges related to high resource consumption and toxic emissions, which are further impacted by the use of performance-enhancing additives. In hydrogen storage systems, tailored additives are required for rubbers to withstand elevated temperatures and high pressures, preventing hydrogen-induced swelling, a major cause of sealing failure. Herein, a novel form of carbonaceous material, carbon nano-onions (CNOs), and the bio-based plasticizer additive epoxidized soybean oil (ESO) are utilized in conventional silica-filled nitrile butadiene rubber (NBR) nanocomposites to develop low-carbon manufacturing high pressure hydrogen resistant O-rings for sealing applications. The results reveal that the incorporation of CNOs increases the crosslinking density (vc), assisted by ESO, in silica-filled NBR nanocomposites. While the conventional adipate-based plasticizer and ESO were found to be susceptible to high pressure hydrogen exposures, ESO demonstrated sustained compressive sealing properties with increase in von-Mises stress and in elevated thermo-oxidative conditions over time. The results of the life cycle assessment (LCA) recommend ESO for low-carbon manufacturing in rubber processing over conventional plasticizer.

Interfacial assembly of nanocellulose microgels enhances thermal insulation of Pickering foam

Nanocellulose has attracted extensive attention in the preparation of thermal insulation materials because of its high Young's modulus, high strength and low thermal expansion coefficient. In this study, nanocellulose microgels prepared by self-assembly of 2,2,6,6-Tetramethylpiperidoxyl oxidized nanocellulose (TOCNC) and Nisin were used as particle stabilizers, and acrylated epoxidized soybean oil (AESO) was used as oil phase to prepare Pickering emulsion, which was cured by heating to obtain biomass-based Pickering thermal insulation foam. Pickering foams prepared based on microgels with different Nisin contents have significant differences in thermal insulation performance. The results show that the addition of microgel particles can improve the thermal stability, increase the roughness of pore wall and reduce the thermal conductivity of AESO polymer foam. Among them, the Pickering foam prepared by microgel containing 0.06 wt% Nisin has the best thermal insulation performance and rougher pore wall surface, and its thermal conductivity is 0.040 W/(m·K), which is obviously lower than that of the foam prepared by TOCNC (0.083 W/(m·K)). Based on the structural design of nanocellulose microgel particles, this work innovatively realized the assembly of microgels at the oil-water interface and the regulation of thermal insulation performance through Pickering technology, and developed a biomass-based foam with improved thermal insulation effect, which provides a new idea for expanding the advanced application of nanocellulose in the field of thermal insulation materials.

Fully Atom-Efficient Solvent-Mediated Biopolymer Manufacturing: A Base Case Illustrated with Macromolecular Surfactants Tailored to Stable Polymer-Water Interfaces.

This work introduces a novel 1-pot, 0-waste, 0-VOC methodology for synthesizing polymeric surfactants using acrylated epoxidized soybean oil and acrylated glycerol as primary monomers. These macromolecular surfactants are synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization, allowing for tunable hydrophilic-lipophilic balance (HLB) and ionic properties. We characterize the copolymers' chemical composition and surface-active properties, and evaluate their effectiveness in forming and stabilizing emulsions of semiepoxidized soybean oil and poly(acrylated epoxidized high oleic soybean oil). Comprehensive analyses, including gel permeation chromatography, nuclear magnetic resonance spectroscopy, dynamic light scattering, particle size distribution, zeta potential, and critical micelle concentration, provide detailed insights into the copolymers and the emulsions they form. The results demonstrate that the RAFT-polymerized surfactants offer long-lasting stability and effectively disperse both common oil-in-water emulsions and highly viscous and hydrophobic polymer latexes. These surfactants outperform traditional small molecule surfactants by reducing particle size and preventing phase separation, even over extended storage periods. Stable polymer-water interfaces are achieved through HLB control, tailored by monomer composition, and the final product requires no additional purification since polymerization occurs in liquid surfactants. While small molecules contribute to rapid micelle formation, the polymeric components enhance long-term stability through steric repulsion and slower dynamics. This method enables even the emulsification of polymers with submicron particle size, which ordinarily requires emulsion polymerization. Integrating biobased polymeric surfactants with advanced polymer processing techniques opens new possibilities for transforming highly hydrophobic polymers into latexes, facilitating downstream applications. This innovation enhances the environmental sustainability of surfactant production and broadens the potential for polymer emulsification technologies. Additionally, the integrated solution-processing approach demonstrated here can be applied to other emerging polymers, where judiciously selected nonvolatile solvents facilitate the polymerization and play a role in the final application.

Novel Determination of Functional Groups in Partially Acrylated Epoxidized Soybean Oil.

The acrylation degree of vegetable oils plays a relevant role in determining the mechanical properties of the resulting polymers. Both epoxide and acrylate functionalities participate in polymerization reactions, producing various types of chemical bonds in the polymer network, which contribute to specific properties such as molecular size distribution, crosslinking degree, and glass transition temperature (Tg). The accurate identification of epoxide and acrylated groups in triglyceride molecules helps to predict their behavior during the polymerization process. A methodology based on analytical spectrometric techniques, such as direct infusion, mass spectrometry with electrospray ionization, and ultra-high-performance liquid chromatography, is used in combination with FTIR and 1H NMR to characterize the epoxy and acrylic functionalities in the fatty chains with different numbers of carbon atoms of partially acrylated triglycerides obtained by a non-catalytic reaction.

Influence of polar‐modified ESBO on the thermal and mechanical properties of FKM/EPDM rubber blends

AbstractRenowned for its oil, heat, and chemical resistance, fluoroelastomer rubber (FKM) also presents notable drawbacks, such as inferior low‐temperature performance. In this study, 2,2‐trifluoroethylamine (TF) and 2,4‐difluorobenzylamine (DF) were grafted onto epoxidized soybean oil (ESBO) to generate two innovative plasticizers: ESBO‐TF and ESBO‐DF that they were specifically designed to augment the low‐temperature performance of FKM. A thorough investigation into the effects of ESBO‐TF/DF on FKM/EPDM blends' properties was conducted. The study demonstrated that the integration of ESBO‐TF and ESBO‐DF enhanced the vital properties of the FKM/EPDM blends, including elongation at break, tear strength, and, significantly, low‐temperature performance. There was a noticeable decrease in the glass transition temperature (Tg), dropping by 3.54 and 2.95°C with the incorporation of 10 phr ESBO‐TF and ESBO‐DF, respectively. These respective plasticizers showed positive effects on the plasticization and compatibilization of the FKM/EPDM blends, thus proposing a novel methodology for developing new plasticizers for FKM and related blends.

Manipulate dynamic chemical interactions in renewable polymers for 3D printing tunable, healable, and recyclable metamaterials

Mechanical metamaterials have garnered significant interests due to their unique properties, which arise from the periodic structures of their constituent units. However, traditional mechanical metamaterials suffer from limitations of fixed properties of the constituent units or irreversibility if they are damaged or little-to-no recyclability. Addressing this challenge, herein, a photoresin consisting of a monomer synthesized from a renewable biomass—epoxidized soybean oil (ESO)—citric acid (CA) and other components was developed for light-based 3D printing. It is discovered that the UV irradiation initiates photopolymerized of the highly photoactive epoxidized soybean oil-ethyl acrylamide (ESO-EA) monomer while enabling the epoxy-acid reaction (EAR) of the epoxy groups in ESO-EA with carboxyl groups in CA to create dynamic chemical bonds (DCBs). This formed dynamic crosslinking network endows the printed material with tunable tensile strengths (0.3–10.4 MPa) and shape memory behaviors (transition temperature: 22–48 °C) while maintaining high stretchability (fractural strain: 81 %–205 %). Thermal annealing facilitates dynamic transesterification reactions (DTER) to further improve the mechanical properties while making the printed materials healable and recyclable. By integrating these innovations into liquid crystal display (LCD) based 3D printing, we demonstrate origami metamaterials with tunable, multi-stable mechanical behaviors as well as property recovery after self-healing of the damaged structures by both simulations and experiments. Finally, the printed metamaterials can be recycled with the well-preserved properties.

Multifractal signatures of light-driven self-organization in acrylated epoxidized soybean oil polymers

Multifractal properties of acrylated epoxidized soybean oil with and without a photoinitiator have been investigated. Using multifractal detrended fluctuation analysis, the photopolymerization process is analyzed by varying illumination duration and intensity. The research is conducted in two stages: the results concerning temperature fluctuations of the entire photoirradiation process are initially presented followed by a sliding window procedure to monitor system complexity during light cycling. Various multifractal mea-sures including the generalized Hurst exponent h(q), the multifractal Rényi exponent τ(q), the generalized fractal dimensions D(q) with the left and right side curvature (ΔDL, ΔDR), the multifractal singularity exponents α, the multifractal spectrum f (α), and the multifractal heat capacity C(q) with its integrated characteristic Carea are examined for both initial and shuffled series. The empirical results demonstrate that the moments of switching on and switching off photoirradiation are characterized by an instantaneous increase in the degree of multifractality of the system. It is hypothesized that the observed increase in multi-fractality at the light-switching-on/off stages is indicative of a quasi-phase transition, which may be associated with the transformation of orientational defects in the polymer network.

Synthesis and characterization of bioplastics based on silyated starch and acrylated epoxidized soybean oil

In the study, the bioplastics were prepared by coupling silylated starch with acrylated epoxidized soybean oil (AESO) at various curing temperatures. 3-aminopropyltriethoxy silane (APTES) was grafted onto starch by the condensation between Si-OH and C-OH. As demonstrated by FTIR and silica content analysis, starch was successfully modified by APTES. The compatibility between silylated starch and AESO was weak as observed by FESEM. The appearance of C-N bonds confirmed the reaction between AESO and silylated starch. An apparent increase of tensile strength from 8.03 MPa to 14.12 MPa was discovered when the bioplastics were cured from 80 °C to 120 °C. Opacity of the bioplastics was enhanced remarkably by AESO due to the incompatibility of silylated starch and AESO. Water resistance test showed that the bioplastics were less sensitive to water after the addition of AESO. The bioplastics maintained good biodegradability after the introduction of AESO. However, increasing the curing temperatures of the bioplastics yielded weak effects on the water resistance and enzymatic degradation of the bioplastics. The bioplastics with excellent mechanical and water-resistant properties were synthesized via the incorporation of AESO under high-temperature curing. The property changes are highly desirable for packaging applications.

Synthesis and biological activity of surface active substances based on epoxidized soybean oil

Synthesis and biological activity of surface active substances based on epoxidized soybean oil

An Assessment of the Properties of Green Composites Utilizing a Variety of Bio‐Based Crosslinkers

AbstractBio‐based materials as crosslinkers for composites have gained attention for their nontoxic, cost‐effective benefits. Using eco‐friendly crosslinkers enhances the properties of the composites and promotes sustainable manufacturing practices too. This study aimed to compare the efficacy of citric acid (CA), itaconic acid (IA), and tannic acid (TA), derived from plant‐based sources, as crosslinkers in the creation of green composites. In this work, compression molding technique was employed for producing composites using coconut fiber as the reinforcing agent and methacrylic anhydride modified epoxidized linseed soybean oil (MAELSO) as the resin. The amount of crosslinkers was varied between 5, 10, and 15 (wt%) to achieve this. Nuclear magnetic resonance spectroscopy confirmed the successful modification of the resin. Fourier transform infrared spectroscopy revealed interactions between components of the composites. Biocomposites loaded with 5 wt% of CA showed 1268 and 92% increase in tensile strength and 1098 and 49% increase in flexural strength compared to those of similar wt% of TA‐ and IA‐based composites respectively. Similarly, the impact strength for CA‐based composite was 84.94 J/m against 168.74 J/m for IA and 330.85 J/m for TA‐based composites. Additionally, composites containing 5 wt% CA exhibited the highest levels of chemical resistance, flame retardancy, and thermal stability. Thus the results suggest that citric acid can serve as an effective crosslinker to fabricate environmentally acceptable composite materials that are suitable for long‐term use. This is noteworthy as it can pave the way for the production of sustainable and eco‐friendly materials, which can be used in various industrial and commercial applications.

Mechanochemical Upcycling of Waste Polypropylene into Warm-Mix Modifier for Asphalt Pavement Incorporating Recycled Concrete Aggregates.

To solve the problems on resource utilization and environmental pollution of waste concrete and waste polypropylene (PP) plastics, the recycling of them into asphalt pavement is a feasible approach. Considering the high melting temperature of waste PP, this study adopted a thermal-and-mechanochemical method to convert waste PP into high-performance warm-mix asphalt modifiers (PPMs) through the hybrid use of dicumyl peroxide (DCP), maleic anhydride (MAH), and epoxidized soybean oil (ESO) for preparing an asphalt mixture (RCAAM) containing recycled concrete aggregate (RCA). For the prepared RCAAM containing PPMs, the mixing temperature was about 30 °C lower than that of the hot-mix RCAAM containing untreated PP. Further, the high-temperature property, low-temperature crack resistance, moisture-induced damage resistance, and fatigue resistance of the RCAAM were characterized. The results indicated that the maximum flexural strain of the RCAAM increased by 7.8~21.4% after using PPMs, while the sectional fractures of the asphalt binder were reduced after damaging at low temperature. The use of ESO in PPMs can promote the cohesion enhancement of the asphalt binder and also improve the high-temperature deformation resistance and fatigue performance of the RCAAM. Notably, the warm-mix epoxidized PPMA mixture worked better close to the hot-mix untreated PPMA mixture, even after the mixing temperature was reduced by 30 °C.

Biopolyol synthesis via ring-opening of epoxidized soybean oil with glycerol utilizing a novel sulfonic-functionalized ionic liquid as the catalyst at low temperature

Herein, a novel synthetic strategy for the preparation of soybean oil-based biopolyol has been established using ionic liquids (ILs) as the green and efficient catalysts via the ring-opening reaction of epoxidized soybean oil (ESO) with glycerol as the nucleophile. Among them, the sulfonic-functionalized IL 1-butylsulfonic-3-methylimidazolium trifluoromethanesulfonate ([BSO3HMIM]OTF) exhibited superior catalytic performance in the ring-opening reaction under mild reaction conditions, demonstrating excellent catalytic efficiency and a high hydroxyl number of the synthesized biopolyol products. The impacts of various reaction variables on the ring-opening reaction were systematically investigated employing one variable at a time (OVAT) and response surface methodology (RSM). Under the optimized reaction parameters, including a catalyst loading of 1.2 wt%, a reaction duration of 4 h, a molar ratio of glycerol to epoxy groups of 3:1, and a tert-butanol to substrate of 1:1 (w/w) at 45 °C, the highest epoxy group conversion rate and the hydroxyl number were found to be 98.0 ± 0.6 % and 285.0 ± 1.4 mg KOH/g, respectively. Characterization by NMR and FT-IR confirmed the successful synthesis of biopolyols, while thermal stability and rheological studies further highlighted their suitability for diverse industrial applications as valuable chemical intermediates. These findings underscore the potential of sulfonic-functionalized [BSO3HMIM]OTF IL as efficient and eco-friendly catalyst in sustainable biopolyol production.

Shape memory and mechanical properties of ESO modified epoxy/polyurethane semi-interpenetrating polymer networks for smart plaster

While numerous studies have explored the potential of shape memory materials in medical applications, the current research output is not enough for significant productivity in industrial products. In this research, a type of shape memory orthopedic plaster was fabricated by using epoxy/polyurethane interpenetrating networks modified with epoxidized soybean oil (ESO) and then compared with some commercial plasters. Polymer networks that were produced could be tailored to have glass transition temperatures (Tgs) within the range of 70–90 °C by changing the percentage composition of polyurethane and soybean oil. Shape recovery and fixity ratios in all samples were above 95 and 97 %. DMA results showed that IPNs with variable amount of soybean oil had lower glass transition temperature (Tg) and cross-link densities compared to IPNs without soybean oil. Based on the tensile test results, most samples exhibited an elastic modulus in the range of 280–400MPa, a level deemed somewhat acceptable when compared to commercial samples. Light microscope images had shown that the increase of polyurethane led to the phase separation of polymers, which was improved by the addition of soybean oil.

Effect of epoxidized soybean oil on melting behavior of poly(l-lactic acid) and poly(d-lactic acid) blends after isothermal crystallization

Abstract The effect of epoxidized soybean oil (ESO) on homocrystallization (HC) and stereocomplex (SC) formation behavior of poly(l-lactide) (PLLA) and poly(d-lactide) (PDLA) bends was investigated utilizing differential scanning calorimetry (DSC). Isothermal crystallization was performed on ESO/PLLA/PDLA blends with varying ESO contents (0, 5, 8, and 10 wt%) and temperatures (90 °C, 120 °C, and 150 °C) for a different duration (12.5, 25, and 125 min). It was found that the ESO could effectively inhibit HC crystallization and promote SC crystallization. For the sample without ESO (ESO-0), the isothermal crystallization temperature and duration had little effect on the melting behavior, whereas sample with 5 wt% ESO (ESO-5), HC crystallization decreased while SC crystallization continued to increase with increasing duration. Additionally, at higher crystallization temperatures with constant ESO content, the melting temperature of SC crystals did not significantly change, suggesting that ESO did not degrade PLLA/PDLA blends. These findings imply that ESO modifies crystallization kinetics, suppressing HC formation and enhancing SC formation, which could benefit for specific material properties and applications.

Fabrication of fire-retarded epoxy asphalt composites with compatibilization and toughening for road tunnel pavements

Although epoxy asphalt (EA) mixtures have been widely used for the pavement in tunnels, it was limited by its flammability, poor compatibility and low mechanical property. To solve the above problems, a compatibilized and toughening flame retardant (ESO-AA-DOPO) was prepared via the epoxidized soybean oil (ESO), arachidonic acid (AA) and 9,10-Dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO). The presence of ESO-AA-DOPO significantly improved the flame retardancy, in which passing the UL-94 V-2 rating. The peak heat release rate (PHRR) reducing by 46.2 % for EA/40A-ESO-AA-DOPO composites comparing to that of pure EA. The analysis of char residue confirmed that the catalytic formation of dense and continuous char layer residue with good thermal oxidation stability originating from the ESO-AA-DOPO. The initial stage viscosity of ESO-AA-DOPO modified EA was lower than that of pure EA. Under the action of aliphatic epoxy resin and double bond, the molecular chain of epoxy resin presented a network structure, the base asphalt was divided into micelles, and the overall distribution of EA system was a 3D networks “sea-island”, which ensuring the increase in the glass transition temperature (Tg) of the EA system. The tensile strength and elongation at break of EA/40A-ESO-AA-DOPO composites were 123 % and 207 % higher than those of pure EA attributing to the improved compatibility and the formation of 3D networks “sea-island” structure.

Nanocomposites based on MWCNT and nanoclay: Effect of acrylated epoxidized soybean oil on curing and composite properties

UV and thermal-curing hybrid epoxy adhesives are generally developed with a combination of epoxy acrylates and thermal-curing epoxy resin. This study modified bisphenol-A type epoxy resin (ER) with acrylated epoxidized industrial crop soybean oil (AESO) to obtain a dual-curable epoxy system. Hydroxylated multi-walled carbon nanotube (MWCNTOH) and montmorillonite-type nanoclay (NC) first was used as nano reinforcement in this system. Both thermal and UV-curing were applied to composites. Tensile and hardness tests, thermogravimetric analysis (TGA), and four-point probe electrical conductivity measurements were used for the nanocomposite characterization. Although (UV+thermal) curing increased the thermal strength of the nanocomposites, it caused a decrease in their electrical conductivity and moisture absorption. The highest tensile strength values were obtained as 107 MPa and 97 MPa for thermally cured 1.5 wt% MWCNTOH and 2 wt% NC composites, respectively. The effect of the AESO ratio on UV curing of nanocomposites was investigated and 10 % was found to be the most suitable. MWCNTOH composites also exhibited the highest electrical conductivity with a percolation threshold of 1.5 wt%. The effect of hydrothermal aging on thermal and electrical conductivity properties showed that only T5 and T10 values of thermally or (UV+thermally) cured MWCNTOH and NC composites decreased, T50 values did not change significantly.

Ionic Liquid Catalysis in Cyclic Carbonate Synthesis for the Development of Soybean Oil-Based Non-Isocyanate Polyurethane Foams.

A method for obtaining non-isocyanate polyurethane (NIPU) foams from cyclic carbonate (CC) based on soybean oil was developed. For this purpose, cyclic carbonate was synthesized from epoxidized soybean oil and CO2 using various ionic liquids (ILs) as catalysts. Among the tested ILs, the highest selectivity (100%) and CC yield (98%) were achieved for 1-ethyl-3-methylimidazolium ([emim]Br). Without any purification, the resulting cyclic carbonate was reacted directly with diethylenetriamine as a model crosslinking agent to produce NIPU foams. It was found that the soybean oil-based CC synthesized with bromide imidazolium ionic liquids exhibited significantly shorter gelling times (8 min 50 s for [emim]Br and 9 min 35 s for [bmim]Br) compared to those obtained with the conventional TBAB catalyst (26 min 15 s). A shorter gelling time is a crucial parameter for the crosslinking process in foams. The obtained foams were subjected to mechanical tests and a morphology analysis.

Flame-retardant and tough poly(lactic acid) with well-preserved mechanical strength via reactive blending with bio-plasticizer and phosphorus derivative

With sustainable development, advanced poly(lactic acid) (PLA) with superior toughness and flame retardancy is highly demanded in various industries, but the current design strategies often fail to achieve such bioplastics. In this work, flame-retardant and tough PLA bioplastics with well-preserved thermal stability and mechanical strength and enhanced UV resistance and soil degradation are prepared by solvent-free, reactive blending of PLA, bio-based epoxidized soyabean oil (ESO) and 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO). With the introduction of 10.0 wt% ESO and 3.0 wt% DOPO, the resultant PLA/10E/3D bioplastic has a high tensile strength of 52.8 MPa, with 26.3 times and 67.5 % increases in elongation at break and impact strength compared to those of PLA due to the toughening effect of ESO and the rigid structure of DOPO. The superior toughness of PLA/10E/3D enables it to outperform previous flame-retardant PLA counterparts. PLA/10E/3D achieves a vertical burning (UL-94) V-0 classification and a limiting oxygen index (LOI) of 27.5 %, indicative of satisfactory flame retardancy. Compared with PLA, PLA/10E/3D maintains high thermal stability and shows significantly enhanced UV-protecting and soil degradation properties. Therefore, this work delivers a green and scalable reactive processing method to create flame-retardant, tough yet strong bioplastics with improved soil decomposition and UV resistance, which contributes to sustainable development.

Fabricating High Strength Bio-Based Dynamic Networks from Epoxidized Soybean Oil and Poly(Butylene Adipate-co-Terephthalate).

Amid the rapid development of modern society, the widespread use of plastic products has led to significant environmental issues, including the accumulation of non-degradable waste and extensive consumption of non-renewable resources. Developing healable, recyclable, bio-based materials from abundant renewable resources using diverse dynamic interactions attracts increasing global attention. However, achieving a good balance between the self-healing capacity and mechanical performance, such as strength and toughness, remains challenging. In our study, we address this challenge by developing a new type of dynamic network from epoxidized soybean oil (ESO) and poly(butylene adipate-co-terephthalate) (PBAT) with good strength and toughness. For the synthetic strategy, a thiol-epoxy click reaction was conducted to functionalize ESO with thiol and hydroxyl groups. Subsequently, a curing reaction with isocyanates generated dynamic thiourethane and urethane bonds with different bonding energies in the dynamic networks to reach a trade-off between dynamic features and mechanical properties; amongst these, the thiourethane bonds with a lower bonding energy provide good dynamic features, while the urethane bonds with a higher bonding energy ensure good mechanical properties. The incorporation of flexible PBAT segments to form the rational multi-phase structure with crystalline domains further enhanced the products. A typical sample, OTSO100-PBAT100, exhibited a tensile strength of 33.2 MPa and an elongation at break of 1238%, demonstrating good healing capacity and desirable mechanical performance. This study provides a promising solution to contemporary environmental and energy challenges by developing materials that combine mechanical and repair properties. It addresses the specific gap of achieving a trade-off between tensile strength and elongation at break in bio-based self-healing materials, promising a wide range of applications.