Acrylated Epoxidized Soybean Oil Research Articles

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.

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.

Development and characterization of UV‐curable PCL/AESO/CNT nanocomposites for biomedical engineering

AbstractThis study investigates the development and characterization of UV‐curable Poly(ε‐caprolactone) (PCL), Acrylated Epoxidized Soybean Oil (AESO), and Carbon Nanotubes (CNT) nanocomposites for biomedical engineering applications. The PCL/AESO blends were prepared in various ratios, and CNTs were incorporated at concentrations of 0.5, 1.0, and 1.5 wt% to enhance mechanical properties. The UV‐curable formulations aimed to leverage rapid curing times, precise control over material properties, and the ability to fabricate complex structures. Results indicated that the incorporation of CNTs improved the tensile strength, modulus, and toughness of the composites. The PCL/AESO/CNT nanocomposites exhibited a tensile strength increase of 25%, a modulus improvement of 30%, and a toughness enhancement of 20% compared to pure PCL. Thermal analysis showed an increase in crystallization temperature and thermal stability, with a crystallinity degree of 63.31% and a maximum degradation temperature of 407°C for the B/C 50/50/1.5 sample. Biocompatibility assessments using L929 fibroblast cells revealed that the composites supported cell viability and proliferation over 7 days with negligible cytotoxicity. Cell attachment studies indicated favorable morphology and adherence, suggesting a conducive environment for cell growth and differentiation. Hydrolytic biodegradation studies demonstrated adjustable degradation rates, making these composites suitable for various biomedical applications requiring controlled biodegradation.

Modification on Fiber from Alkali Treatment and AESO Coating to Enhance UV-Light and Water Absorption Resistance in Kapok Fiber Reinforced Polyester Composites

ABSTRACT Environmental contamination poses a significant threat to the integrity of materials, including metals and composites. Addressing the degradation of natural fiber-reinforced polymer composites necessitates effective management strategies, particularly in mitigating UV and water-induced deterioration. This study explores the efficacy of Acrylated Epoxidized Soybean Oil (AESO) coating treatment following alkali treatment as a potential solution. Alkali treatment of Kapok fiber (KF) combined with polymer coating yielded composites exhibiting superior mechanical properties, particularly in tensile and flexural strength, following a 30-day aging period. Remarkably, the application of alkali and coating treatments led to a substantial enhancement in the mechanical strength of polyester composites, with the highest tensile strength recorded at 96.04 MPa. This represented a notable increase of 31.97% compared to untreated KF specimens. The observed enhancement in composite performance underscores the critical role of interfacial adhesion between fibers and the matrix, particularly under conditions of UV exposure and water immersion. Importantly, the study demonstrates that alkali treatment and polymer coating effectively mitigate degradation in Natural Fiber-Reinforced Polymer Composites, thereby offering promising avenues for enhancing their durability and longevity.

Quinizarin-based photoactive porous polymers from emulsion templates: Monoliths versus membranes in photobactericidal applications

The increasing challenge of antimicrobial resistance and the persistent threat of infectious diseases are strong incentives for development of novel materials that effectively and sustainably combat bacterial proliferation. Macroporous materials contribute to this endeavor, but the reported antibacterial porous polymers rely on the release of antibacterial agents, which carries the risk that their efficacy will diminish over time. This work reports a facile synthesis by emulsion templating polymerization of innovative photo-bactericidal macroporous polymers functionalized by a quinizarin photosensitizer that generates antibacterial reactive oxygen species under visible light. In brief, a monomethacrylated quinizarin (QMA) derivative, known for its ability to generate bactericidal singlet oxygen upon visible light irradiation, is copolymerized with a bio-based acrylated epoxidized soybean oil (AESO) under high internal phase emulsion (HIPE) conditions, resulting in 3D-interconnected quinizarin-functionalized macroporous monoliths. The QMA-functionalized polyHIPEs are also structured into membranes by photocuring thin layers of HIPEs to increase their external surface and promote interaction with light. Photobleaching tests show the ability of these materials to generate bactericidal singlet oxygen. Antibacterial tests also demonstrate the sustained antibacterial efficacy of the QMA-based porous membranes, providing a promising avenue for the development of next-generation antibacterial materials.

Optimizing biobased thermoset resins by incorporating cinnamon derivative into acrylated epoxidized soybean oil

The study successfully developed thermoset materials utilizing acrylate epoxidized soybean oil (AESO) and allyl cinnamate (ACIN) with tert-butyl peroxybenzoate (TBPB) as the initiator. Isothermal curing at temperatures between 110 °C to 140 °C of the developed formulations, showed that higher temperatures accelerated the conversion process. The higher curing temperature increased the degree of conversion, leading to obtain the best flexural strength for samples cured at 130 °C. However, samples cured at 120 °C exhibited better impact properties due to a lower degree of conversion, which allows for a more mobile reticular network. In addition, morphological observations confirmed these mechanical property trends. Dynamic thermal characterization revealed changes in glass transition temperature and exothermic reactions due to unreacted products appeared for materials cured at low temperature. Increasing curing temperature allowed to enhance thermal stability by increasing molecular weight. Finally, thermomechanical analysis confirmed stiffness and glass transition temperature increases observed during flexural tests and thermal characterization.

Production and characterization of novel biodegradable films using fruit industrial waste and aloe vera gel

One of the huge volumes of fruit waste that is a concern for waste management challenges today is the fruit juice industry sour cherry kernel (SCK) waste. The gel obtained by processing the leaf extract of aloe vera (AVG) is the most commercial aloe species and has become a major industry worldwide. This study used AVG and SCK as an additive in acrylated epoxidized soybean oil (AESO) to prepare biobased film materials. Two types of processes were used in curing the films: UV curing from acrylate groups and thermal curing from epoxide groups of AESO. The effect of additive type and amount on antibacterial activity, mechanical, swelling, mass loss, and water vapor permeability properties of the films were investigated. The produced films were characterized using FTIR spectra. Thermal properties were investigated by thermogravimetric analysis (TGA). The biodegradability of AESO was determined as 7.095%. In comparison, the highest biodegradation was observed in films with 50% additive content and this value was measured as 8.89% and 39.95% for AVG- and SCK-containing films, respectively. In addition, the corrosion tests of the films were also carried out and the films with SCK additives were more resistant to corrosive environments. Data were analyzed using an ANOVA test.Graphical abstract

Fully Bio-Based Polymer Composites: Preparation, Characterization, and LCD 3D Printing.

The present work aimed to prepare novel bio-based composites by adding fillers coming from agro-wastes to an acrylate epoxidized soybean oil (AESO) resin, using liquid crystal display (LCD) 3D printing. Different photocurable formulations were prepared by varying the reactive diluents, iso-bornyl methacrylate (IBOMA) and tetrahydrofurfuryl acrylate (THFA). Then, two fillers derived from different industrial wastes, corn (GTF) and wine (WPL-CF) by-products, were added to the AESO-based formulations to develop polymer composites with improved properties. The printability by LCD of the photocurable formulations was widely studied. Bio-based objects with different geometries were realized, showing printing accuracy, layer adhesion, and accurate details. The thermo-mechanical and mechanical properties of the 3D-printed composites were tested by TGA, DMA, and tensile tests. The results revealed that the agro-wastes' addition led to a remarkable increase in the elastic modulus, tensile strength, and glass transition temperature in the glassy state for the systems containing IBOMA and for flexible structures in the rubbery region for systems containing THFA. AESO-based polymers demonstrated tunable properties, varying from rigid to flexible, in the presence of different diluents and biofillers. This finding paves the way for the use of this kind of composite in applications, such as biomedical for the realization of prostheses.

Impact of chemical composition of soybean oil and vanillin-based photocross-linked polymers on parameters of electrochemical biosensors

Network properties on local free volume and biosensor parameters of polymers based on acrylated epoxidized soybean oil (AESO), a combination of AESO with vanillin dimethacrylate (VDM) in ratio 1:0.25 mol, and its combination with vanillin diacrylate (VDA) with the same molar ratio, used as laccase-holding matrixes for the construction of amperometric biosensors, were tested and compared. The formed polymer matrixes were investigated using Positron Annihilation Lifetime Spectroscopy (PALS) as bulk samples and applying electrochemical methods as sensor films. PALS results showed that the lifetime of the ortho-positronium component and corresponding intensity are almost similar for both polymers, indicating no significant difference from the point of view of their morphology. However, the cyclic voltammetric and chronoamperometric analysis demonstrated significant differences in the bioelecrodes’ operational parameters formed by the AESO:VDM polymer compared to AESO:VDA. The AESO:VDA-based bioelectodes were characterized with a twice higher affinity toward ABTS (KMapp = 0.158 ± 0.022 mM vs. 0.326 ± 0.043 mM). At the same time, their sensitivity was about twice less compared to AESO:VDM-based (902 A·M−1·m−2vs. 1608 A·M−1·m−2), and a start concentration of the linear frame was 7-folds higher (14 μM vs. 2 μM ABTS). It was shown early, that the operational parameters of amperometric biosensors are greatly dependent on morphological characteristics of polymer matrixes (e.g., crosslink density, cavities size, thermal expansion of free-volume hole, etc.). The matrix morphology affects on efficacity of physical diffusion of the substrate to the enzyme, and electroactive product toward the electrode, as well as provides a comfortable environment for the incorporated enzyme. Here, we describe the usage of polymer matrixes with the same morphological properties but different chemical compositions, analyzing the effect of chemical structure on the operational parameters of biosensors. Thus, it was demonstrated that the sensor operational parameters depend not only on the morphological properties of the polymer holding matrixes, providing enzyme fixation and substrate/product diffusion, but also on their chemical composition, which opens a possibility to adapt the biosensor characteristics according to the required needs of analysis.

In vitro evaluation of bone cell response to novel 3D-printable nanocomposite biomaterials for bone reconstruction.

Critically-sized segmental bone defects represent significant challenges requiring grafts for reconstruction. 3D-printed synthetic bone grafts are viable alternatives to structural allografts if engineered to provide appropriate mechanical performance and osteoblast/osteoclast cell responses. Novel 3D-printable nanocomposites containing acrylated epoxidized soybean oil (AESO) or methacrylated AESO (mAESO), polyethylene glycol diacrylate, and nanohydroxyapatite (nHA) were produced using masked stereolithography. The effects of volume fraction of nHA and methacrylation of AESO on interactions of differentiated MC3T3-E1 osteoblast (dMC3T3-OB) and differentiated RAW264.7 osteoclast cells with 3D-printed nanocomposites were evaluated in vitro and compared with a control biomaterial, hydroxyapatite (HA). Higher nHA content and methacrylation significantly improved the mechanical properties. All nanocomposites supported dMC3T3-OB cells' adhesion and proliferation. Higher amounts of nHA enhanced cell adhesion and proliferation. mAESO in the nanocomposites resulted in greater adhesion, proliferation, and activity at day 7 compared with AESO nanocomposites. Excellent osteoclast-like cells survival, defined actin rings, and large multinucleated cells were only observed on the high nHA fraction (30%) mAESO nanocomposite and the HA control. Thus, mAESO-based nanocomposites containing higher amounts of nHA have better interactions with osteoblast-like and osteoclast-like cells, comparable with HA controls, making them a potential future alternative graft material for bone defect repair.

Improving the 3D Printability and Mechanical Performance of Biorenewable Soybean Oil-Based Photocurable Resins.

The general requirement of replacing petroleum-derived plastics with renewable resources is particularly challenging for new technologies such as the additive manufacturing of photocurable resins. In this work, the influence of mono- and bifunctional reactive diluents on the printability and performance of resins based on acrylated epoxidized soybean oil (AESO) was explored. Polyethylene glycol di(meth)acrylates of different molecular weights were selected as diluents based on the viscosity and mechanical properties of their binary mixtures with AESO. Ternary mixtures containing 60% AESO, polyethylene glycol diacrylate (PEGDA) and polyethyleneglycol dimethacrylate (PEG200DMA) further improved the mechanical properties, water resistance and printability of the resin. Specifically, the terpolymer AESO/PEG575/PEG200DMA 60/20/20 (wt.%) improved the modulus (16% increase), tensile strength (63% increase) and %deformation at the break (21% increase), with respect to pure AESO. The enhancement of the printability provided by the reactive diluents was proven by Jacobs working curves and the improved accuracy of printed patterns. The proposed formulation, with a biorenewable carbon content of 67%, can be used as the matrix of innovative resins with unrestricted applicability in the electronics and biomedical fields. However, much effort must be done to increase the array of bio-based raw materials.

Fast-curing bio-based thermoset foams produced via the Michael 1,4-addition using fatty acid-based acetoacetate and acrylate

This study introduces an approach for creating bio-based polymer foams exploiting the Michael reaction that could be utilized as thermal insulation. The thermoset foams were developed using a second-generation bio-based feedstock – tall oil. Tall oil is a by-product of wood pulping in paper manufacturing and mainly comprises unsaturated fatty acids like oleic and linoleic acid. The study explores the use of tall oil-based acetoacetates (Michael donor) combined with various acrylates (Michael acceptor), petrochemical-based (bisphenol-A ethoxylate diacrylate, trimethylolpropane triacrylate, pentaerythritol tetraacrylate), and bio-based (epoxidized soybean oil acrylate, epoxidized tall oil free fatty acids-based acrylate), to develop polymer foams that meet today's sustainability requirements. The developed polymer foams underwent extensive characterization. Matrix curing parameters were assessed by measuring changes in dielectric polarization during curing. Foaming parameters, including start and rise times, were precisely measured. The chemical composition of the foams was analysed using Fourier-transform infrared spectroscopy. Their thermal, thermo-mechanical, and mechanical properties were evaluated through thermal gravimetric analysis, differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), and compression tests. Additionally, the content of closed-cell and the coefficient of thermal conductivity were determined, further characterizing the foams as potential thermal insulation materials. Foams from bio-based donors with petrochemical-based acceptors exhibited a range of enhanced properties. They not only achieved high glass transition temperatures (up to 85 °C by DSC and up to 108 °C by DMA) but also displayed a spectrum of mechanical strengths (compression strength ranging from moderate to as high as ∼ 0.40 MPa) and good thermal isolation properties (thermal conductivity coefficient ∼ 31mW/(m·K)). Bio-based foams, derived from renewable resources, were characterized by properties fitting for flexible foam applications, such as low glass transition temperatures (down to −9.7 °C by DSC and down to 9.8 °C by DMA), reduced compression strength (approximately 0.011 MPa), and increased thermal conductivity (up to 46.7mW/(m·K)), indicating their potential utility in applications where flexibility is a key requirement.

High-performance pervious concrete using cost-effective modified vinyl ester as binder

Pervious concrete has a unique open-skeleton structure and high permeability, which effectively control water runoff, mitigate urban heat island effects, and reduce traffic noise in urban constructions. However, low strength, easy granulation, and poor durability often limit its application in pavement engineering. As a polymer binder, vinyl ester (VE) resin has high strength, wear resistance, durability, and corrosion resistance, which can remedy the shortage of pervious concrete. In this work, by optimizing the aggregate gradation and curing temperature, high-performance pervious concrete using VE resin as binder was fabricated. To further improve the performance of VE binder, renewable acrylated epoxidized soybean oil (AESO) and diphenylmethane diisocyanate (MDI) were used to increase the crosslinking degree of the resin and the durability of pervious concrete. When using 15% AESO and 10% MDI based on the weight of VE, the pervious concrete achieved an enhanced flexural strength of up to 7.72 MPa. A significant improvement was achieved by incorporating 50 wt% solid wastes copper slag into the pervious concrete, the compressive strength and flexural strength reached 37.72 MPa and 7.53 MPa, respectively. The permeability coefficient of the permeable concrete was 2.64 mm/s, and the connected porosity was 11.33%, which are higher than the requirements of China national standard. The satisfactory durability of pervious concrete was also verified through freeze-thaw, abrasion, and aging tests. This work offers a viable strategy for cost-efficient and sustainable high-performance pervious concrete, providing insights into the utilization of renewable feedstocks and solid wastes in civil materials.

Soybean Oil-Based 3D Printed Mesh Designed for Guided Bone Regeneration (GBR) in Oral Surgery.

This study aims to obtain a cyto-compatible 3D printable bio-resin for the manufacturing of meshes designed from acquired real patients' bone defect to be used in future for guided bone regeneration (GBR), achieving the goal of personalized medicine, decreasing surgical, recovery time, and patient discomfort. To this purpose, a biobased, biocompatible, and photo-curable resin made of acrylated epoxidized soybean oil (AESO) diluted with soybean oil (SO) is developed and 3D printed using a commercial digital light processing (DLP) 3D printer. 3D printed samples show good thermal properties, allowing for thermally-based sterilization process and mechanical properties typical of crosslinked natural oils (i.e., E = 12MPa, UTS = 1.5MPa), suitable for the GBR application in the oral surgery. The AESO-SO bio-resin proves to be cytocompatible, allowing for fibroblast cells proliferation (viability at 72h > 97%), without inducing severe inflammatory response when co-cultured with macrophages, as demonstrated by cytokine antibody arrays, that is anyway resolved in the first 24 h. Moreover, accelerated degradation tests prove that the bio-resin is biodegradable in hydrolytic environments.

Microscale interface mechanism of the improved high and low-temperature performance of modified bamboo fibres-reinforced asphalt mixture

ABSTRACT Using plant fibres to reinforce asphalt mixture and improve its road performance has attracted growing interest. To improve the interfacial adhesion between bamboo fibres (BFs) and asphalt matrix, BFs were treated with acrylate epoxidized soybean oil (AESO) and 4,4'-diphenyl methane diisocyanate (MDI). The high-temperature stability and low-temperature cracking resistance of the modified BFs-reinforced asphalt mixture were evaluated by the rutting and bending experiments, respectively. The dynamic stability at 60°C and the flexural strength at −10°C of the mixture with modified BFs were improved by 21.67% and 22.84%, respectively. Then, molecular dynamic simulations were implemented to investigate the effect of fiber modification on the interface properties. Simulation results showed that as the grafting density increased from 0 to 2.21 × 10–7 mol/m2, the binding energy increased by 277.2% and 159.3% at 65°C and −15°C, respectively, and the diffusion coefficient decreased by 50.8% and 27.7% at 65°C and −15°C, respectively. As the grafting density further increased to 4.43 × 10−7 mol/m2, the interface performance deteriorated because the dense grafted molecular chains inhibited the diffusion of asphalt to BF surfaces. This work provides an understanding of the interfacial mechanism for optimising the BF-reinforced asphalt mixtures.

Non-isothermal curing kinetics of soybean oil-based resins: Effect of initiator and reactive diluent

Soybean oil has been utilized as a raw material to develop biobased polymer to replace petroleum-based counterparts due to its abundance, renewability, and molecular designability. Acrylated epoxidized soybean oil (AESO) is a commercially available product and has been used in coatings, plasticizers, and composites. The curing of AESO resins normally refers to the free-radical polymerization of CC bonds, which is closely related to the types of initiators and reactive diluents (RDs). In this work, the processing parameters and curing kinetic mechanism of AESO resins were investigated based on the extrapolation method, Kissinger, Crane, and Friedman equations, and the influences of initiators and RDs on the curing of the resins were explored. Results indicated that the types of initiators significantly affected the processability and curing kinetics of AESO resins, and the curing temperatures and reaction activation energy of the resins were strongly associated with the decomposition temperature and activation energy of the initiators. The number of CC bonds and molecular structure of RDs considerably influence the curing characteristics of the resins. The addition of RDs endowed the reaction more complexity, and the activation energy significantly depended on the level of CC conversion.

Soybean oil‐based nanocomposites for dye adsorption: AESO‐chitosan‐graphene oxide synergy in water treatment

AbstractThis study presents the synthesis and characterization of a bio‐adsorbent (A‐C2‐G3) based on the acrylated epoxidized soybean oil (AESO) for the efficient removal of methylene blue (MB) dye from aqueous solutions. The adsorbent was synthesized by incorporating chitosan and nano graphene oxide into the AESO matrix, followed by crosslinking through the UV curing process. The effects of various parameters, including pH, contact time, initial dye concentration, adsorbent dosage, and ionic strength, on the adsorption performance were systematically investigated. The experimental data were best fitted by the Langmuir isotherm model, suggesting a monolayer adsorption process, with a maximum adsorption capacity of 263.87 mg g−1. The adsorption kinetics followed the pseudo‐second‐order model, indicating the significance of electron exchange between the adsorbate and adsorbent during the process. Three primary interaction mechanisms at the interface between MB and A‐C2‐G3 and the A‐C2‐G3 bio‐adsorbent were identified: electrostatic interactions, hydrogen bond formation, and π–π stacking. The reusability of the synthesized adsorbent was evaluated through a series of adsorption–desorption cycles, maintaining high adsorption capacities for up to three cycles. These findings highlight the potential of the AESO‐based bio‐adsorbent for effective MB dye removal from wastewater.

Effect of Aromatic Rings in AESO-VDM Biopolymers on the Local Free Volume and Diffusion Properties of Polymer Matrix

In this work, the influence of aromatic rings on the local free volume of cured mixtures of acrylate epoxidized soybean oil (AESO) and vanillin dimethacrylate (VDM) was investigated. Cross-linking took place under the influence of UV light in the presence or absence of a photoinitiator. The local free volume and its homogeneity were characterized using the Positron Annihilation Lifetime Spectroscopy (PALS) technique. It was found that increasing the content of VDM, which contains aromatic rings, caused a decrease in the local free volume of the cured polymer network, with consequences for the diffusion properties of the polymer, which were tested for the case of water. Another consequence of increasing the content of VDM was a decrease in the conversion of double bonds in the finally cured samples, characterized by near-infrared spectroscopy (NIR). This finding illustrates a case where the decrease in free volume is not necessarily related to an increase in the crosslinking density of the polymer, but is a consequence of the presence of an increase in the occupied volume of aromatic rings in the volume of the polymer.

Optimizing rheological performance of unsaturated polyester resin with bio-based reactive diluents: A comprehensive analysis of viscosity and thermomechanical properties

Bio-based reactive diluents (RD) have been explored as alternative to styrene (STY) in unsaturated polyester resin (UPR). Among the different candidates, acrylated epoxidized soybean oil (AESO) and epoxidized linseed oil (ELO) stand out as triglyceride derivatives. Aditionally, methyl methacrylate (MMA), trimethylolpropane triacrylate (TMPTA) with acrylic functionality, limonene (LIM), and cinnamates (CINN), has been tested in different percentages. Firstly, their efficiency in viscosity reduction has been studied. Best results were obtained after the addition of MMA, LIM, and CINN at 5 wt%. These RD achieve a viscosity reduction of 48.9 %, 76.7 %, and 22.9 %, respectively, compared to the reference sample. The industrial utilization of CINN as RD is impeded by its reactivity, as has been evidenced by its prolonged reaction time (24 min) and low reaction enthalpy. The thermo-mechanical properties studied through flexural tests, Shore D hardness, Charpy's Impact test, and heat deflection temperature (HDT), show that the developed UPRs exhibit a decrease in resistant mechanical properties while doubling their ductility by using LIM and MMA as bio-based RD (1.88 and 2.15 kJ m−2, respectively). The HDT study results demonstrate a certain level of thermal stability when MMA is employed (56 °C), which is 15 % lower in the case of LIM. Therefore, it is observed that UPRs with bio-based RD exhibit balanced and improved thermo-mechanical properties in terms of ductility and strength, especially with the use of a 5 wt % of LIM and MMA.

UV-Cured Bio-Based Acrylated Soybean Oil Scaffold Reinforced with Bioactive Glasses.

In this study, a bio-based acrylate resin derived from soybean oil was used in combination with a reactive diluent, isobornyl acrylate, to synthetize a composite scaffold reinforced with bioactive glass particles. The formulation contained acrylated epoxidized soybean oil (AESO), isobornyl acrylate (IBOA), a photo-initiator (Irgacure 819) and a bioactive glass particle. The resin showed high reactivity towards radical photopolymerisation, and the presence of the bioactive glass did not significantly affect the photocuring process. The 3D-printed samples showed different properties from the mould-polymerised samples. The glass transition temperature Tg showed an increase of 3D samples with increasing bioactive glass content, attributed to the layer-by-layer curing process that resulted in improved interaction between the bioactive glass and the polymer matrix. Scanning electron microscope analysis revealed an optimal distribution on bioactive glass within the samples. Compression tests indicated that the 3D-printed sample exhibited higher modulus compared to mould-synthetized samples, proving the enhanced mechanical behaviour of 3D-printed scaffolds. The cytocompatibility and biocompatibility of the samples were evaluated using human bone marrow mesenchymal stem cells (bMSCs). The metabolic activity and attachment of cells on the samples' surfaces were analysed, and the results demonstrated higher metabolic activity and increased cell attachment on the surfaces containing higher bioactive glass content. The viability of the cells was further confirmed through live/dead staining and reseeding experiments. Overall, this study presents a novel approach for fabricating bioactive glass reinforced scaffolds using 3D printing technology, offering potential applications in tissue engineering.