Improvement Of Interfacial Adhesion Research Articles

Flexible and antistatic carbon fiber/silicone rubber composite coating with improved thermal stability, mechanical and wave-transmission properties

The properties of the interface have a significant impact on the application of silicone rubber (SR) composite coating fillers with carbon fiber (CF). The one-step growth of silica nanoparticles on the fiber surface was investigated in terms of the mechanical, electrical, and thermal properties of the CF/SR composite coatings. The results showed that the tensile strength and elongation of the composite with modified fibers were 7.13 ± 0.44 MPa and 690.40 ± 37.04 %, which were 20.44 % and 23.22 % higher than those with unmodified CFs, respectively. The improvement in interfacial adhesion by silica modification effectively disperses stress and avoids stress concentration. Additionally, the introduction of the low-dielectric material SiO2 and the reduction of the interfacial polarization enhanced the wave-transmission properties and weakened the electromagnetic wave-shielding properties of the composites. Meanwhile, the silica modification maintained the antistatic properties of the coatings at room and high temperatures, as well as before and after bending. The weight loss of the composites with modified fibers was lower than that of the composites with unmodified fibers, while the thermal conductivity was higher because of the stable structure of the Si-O-Si bonds and interfacial adhesion. This work provides a simple way to enhance the thermal resistance, thermal conductivity, mechanical and wave-transmission properties, and preserve the antistatic properties as well as the flexibility of CF/SR composite coatings.

Enhancing the Lap Shear Performance of Resistance-Welded GF/PP Thermoplastic Composite by Modifying Metal Heating Elements with Silane Coupling Agent.

Thermoplastic composites are gaining widespread application in aerospace and other industries due to their superior durability, excellent damage resistance, and recyclability compared to thermosetting materials. This study aims to enhance the lap shear strength (LSS) of resistance-welded GF/PP (glass fiber-reinforced polypropylene) thermoplastic composites by modifying stainless steel mesh (SSM) heating elements using a silane coupling agent. The influence of oxidation temperature, solvent properties, and solution pH on the LSS of the welded joints was systematically evaluated. Furthermore, scanning electron microscopy (SEM) was utilized to investigate the SSM surface and assess improvements in interfacial adhesion. The findings indicate that surface treatment promotes increased resin infiltration into the SSM, thereby enhancing the LSS of the resistance-welded joints. Treatment under optimal conditions (500 °C, ethanol solvent, and pH 11) improved LSS by 27.2% compared to untreated joints.

Improvement of interfacial adhesion of aramid fiber/polycarbonate composites by surface modification with graphene oxide modified sizing agents

AbstractVarious sizing agents were prepared to enhance the interfacial properties between aramid fiber (AF) and polycarbonate (PC), as well as to enhance the mechanical properties of AF/PC composites. It was found that PC sizing agent, P‐GO sizing agent, and PSi‐GO sizing agent effectively coated the surface of AF from the FTIR and XPS and SEM results. The IFSS and mechanical properties of composites reinforced with fibers treated by the sizing agents exhibited significant improvement, as well as their single fiber tensile strength also improved. Specifically, when AF was treated with PSi‐GO sizing agent, the interfacial shear properties between AF and PC increased by a remarkable 78.69%, reaching 22.89 MPa compared to the original AF/PC composite, the tensile strength of the single‐filament exhibited an increment of 12.4% to 26.4 cN/dtex. Moreover, the tensile strength, flexural strength, and impact strength of the composite increased by 5.43%, 77.74%, and 54.71%, respectively. These improvement can be attributed to the GO with a higher concentration of chemical groups and excellent dispersion with modified with the silane agent. These findings suggest that coating the AF with sizing agents can effectively enhance its interfacial adhesion with the matrix, which is useful for its application as the reinforcement in the composites.Highlights Adding GO to the sizing agent to change the Aramid fabric surface properties. Silane coupling agent was used to improve the dispersion of GO on the fiber surface. GO modified sizing agent can improve the flexural strength, tensile strength, and interlaminar shear strength of the composites.

Enhancing GFRP fatigue durability for chassis component applications through glass fiber coupling variation

As the landscape of mobility trends continues to evolve, concerted efforts have been made to incorporate Carbon Fiber Reinforced Plastic (CFRP) into automotive components. However, the substantial increase in cost relative to the achieved weight reduction has limited its widespread adoption. Consequently, research endeavors have focused on exploring alternative composite materials, adapting fibers such as glass fibers, natural fibers, and recycled fibers, to reduce the cost of composite components. Of particular interest in the automotive industry is the utilization of Glass Fiber Reinforced Plastic (GFRP) in chassis components like leaf springs. Nevertheless, the development of GFRP leaf springs encounters a significant challenge related to the adhesive strength at the interface between epoxy resin and glass fibers, which is crucial for enhancing fatigue durability. While glass fibers were traditionally paired with unsaturated polyester or vinyl ester matrices, the pursuit of improved durability has led to the adoption of epoxy matrices. Regrettably, this transition has not consistently yielded the expected gains in interfacial adhesion.In light of these challenges, this study systematically compares the interfacial adhesion strength and fatigue endurance performance. For comparison, two coupling agents widely used commercially, amino silane and epoxy silane, were selected. Glass fibers treated with each coupling agent were purchased commercially, and glass fiber-reinforced plastic (GFRP) specimens were fabricated using the HP-RTM (High-Pressure Resin Transfer Molding) method. Static property evaluations and fatigue durability assessments were conducted using the fabricated specimens. The results showed that when epoxy silane was used as the coupling agent, the interlaminar shear strength (ILSS) increased by approximately 7 %. Furthermore, SEM(Scanning Electron Microscopes) analysis confirmed a significant enhancement in interfacial adhesion, providing support for the ILSS evaluation results. Consequently, the fatigue durability performance improved by approximately six-fold. This confirms that the improvement in interfacial adhesion due to the change in coupling agents led to enhanced fatigue durability performance.

Mechanically robust and electrically conductive nanofiber composites with enhanced interfacial interaction for strain sensing

Electrically conductive fiberfibre/fabric composites (ECFCs) are competitive candidates for use in wearable electronics. Therefore, it is essential to develop mechanically robust ECFC strain sensors with sensing performance. In this study, MXene assembly and hot-pressing were combined to prepare strong yet breathable ECFCs for strain and temperature sensing. Hydrogen bonding between MXene and polyurethane (PU) and ultrasonication-induced interfacial sintering were responsible for MXene nanosheets assembly on the PU nanofibers. MXene decoration made PU nanofibers electrically conductive, resulting in a conductive network. Hot-pressing improved interface adhesion among the conductive nanofibers. Thus, the mechanical properties of the nanofiber composites, including tensile strength, toughness and fracture energy, were enhanced. The nanofiber composites exhibited surface stability and durability. When the nanofiber composites were used as strain sensors, they showed breathability with a linear resistance response ranging from 1 % to 100 % and cycling stability. In addition, they produced stable sensing signals over 1000 cycles when a notch was present. They could also monitor temperature variations with a negative temperature coefficient (−0.146 %/°C). This study provides an interfacial regulation method for the preparation of multi-functional nanofiber composites with potential applications in flexible and wearable electronics.

Experimental and theoretical investigation of the effect of physical and chemical compatibilization on the properties of thermoplastic elastomers derived from natural rubber and polypropylene blends

The objective of this research was to improve the compatibility between Natural Rubber/Polypropylene NR/PP blends through physical and chemical compatibilization methods. The physical compatibilization involved the use of epoxidized natural rubber/maleic anhydride-grafted polypropylene (ENR50/PP-g-MA) as a dual compatibilizing agent (CA50), while the process of reactive compatibilization entailed chemically modifying NR and PP phases through the grafting maleic anhydride (MA). Several formulations were prepared by melt mixing using a Brabender plasti-corder. The effects of physical and chemical compatibilization on the technical properties were investigated. FTIR analysis revealed the emergence of two distinctive peaks corresponding to the CO group of MA grafted onto PP and NR chains. FTIR analysis has also confirmed the taking place of reactions between the polar functional groups of PP-g-MA and ENR50. The rheological properties indicated that the viscosity of the NR-g-MA/PP-g-MA is lower than those of the control blend and CA50-based NR/PP system. The mechanical and dynamic mechanical findings corroborated the improvement of interfacial adhesion between NR/PP phases, especially for the NR/PP/CA50 system. SEM examination demonstrated a more uniform dispersion of the PP phase in the CA50-based NR/PP, compared to the control blend and NR-g-MA/PP-MA. NR-g-MA/PP-g-MA exhibits greater miscibility and interaction potential compared to the control NR/PP, and less than NR/(ENR50/PP-g-MA)/PP system. DFT calculations further validate the effect of compatibilization methods on TPE blends. Specifically, Quantum molecular descriptors revealed the role of ENR50/PP-g-MA as an intermediary in facilitating compatibility between NR/PP. These findings indicate that the physical compatibilization method approach using ENR50/PP-g-MA as a dual compatibilizer is a potential compatibilizer for NR/PP.

Nanoclay protonation and silane functionalization to enhance mechanical and fracture performance of epoxy nanocomposites

AbstractNanoclay is considered to be one of the best fillers for reinforcement in structural polymer composites because of its low cost, easy availability, and ability to improve mechanical, thermal, corrosion resistance, barrier properties and nonflammability in corresponding nanocomposites. Pristine nanoclay is hydrophilic and therefore needs surface modification to make it compatible for uniform dispersion with polymer matrix. In the present work, montmorillonite nanoclay was protonated for generating more hydroxyl groups to facilitate silane functionalization and is reinforced to prepare epoxy nanocomposites with a varying content of 0.5 to 20 wt%. Studies are also conducted to investigate the effect of silanization of unprotonated nanoclay on epoxy nanocomposites. Interestingly, uniform highly exfoliated reduced‐size nanoclay platelets are obtained for functionalized protonated nanoclay. This behavior is attributed to the increase in the d‐spacing between the interlayers of the nanoclay during protonation and silanization. Tensile performances are found best with 0.5 wt% of silanized clay with an improvement of ~50%, ~84% and ~177% in strength, modulus and absorbed failure energy compared to neat epoxy. Although flexural and fracture performance are found highest with 2 wt% of silanized protonated clay with an improvement of ~57.5% in flexural strength and a remarkable ~241% and ~964% enhancement in fracture toughness and fracture energy compared to neat epoxy. The toughening mechanism investigation endorses the improvement in interfacial adhesion of the protonated silanized nanoclay that enhances the properties of the interfacial region, which significantly enhances the resistance for in‐panne crack propagation in epoxy nanocomposites.Highlights Synthesized silanized and silanized protonated montmorillonite clay. Protonation facilitated silane moiety attachment onto nanoclay. Maximum improvement of flexural strength by ~57.5% for ESPrC2. KIC and GIC were highest showing ~1.74 MPam1/2 and ~830.28 J/m2 for ESPrC2. Enhanced interfacial adhesion due to SPrC with the epoxy matrix.

Effect of temperature on interface debonding behavior of graphene/graphene-oxide on cement-based composites

Temperature effect easily affect the adhesion of graphene/graphene oxide (GO) on the cement-based composites originating from the weaker non-covalent bonding at the interface, leading to weakening of the cementitious composite properties. In this study, the interfacial debonding behavior of graphene/GO and cement-based composites was investigated for low to high temperatures (250∼550 K) using controlled molecular dynamics simulations. The maximum tensile force and work of adhesion both decrease with increasing temperature, and the value of GO is 5∼6 times that of graphene. Especially at the high temperature end, GO is still difficult to peel off (Fmax: 7.93×103 pN, Wmax:2129.60 Kcal/mol). Meanwhile, the insights into the distribution and concentration of functional groups have shown that high concentrations and edge functional groups can improve interface adhesion. Energy decomposition demonstrated that, compared to the Coulomb effect of charge and the prestress of surface wrinkles, the van der Waals effect plays a major role in interface adhesion. Entropy analysis further reveals the high temperature sensitivity of graphene and the low sensitivity of GO due to edge functional groups. We believe that the insight into the temperature effect of interface debonding behavior at nanoscale can provide theoretical support for the effective temperature working conditions of graphene/graphene-oxide on cement-based composites.

Revealing the mechanism of interfacial adhesion enhancement between the SiO2 film and the GaAs substrate via plasma pre-treatments

The formation mechanism of a highly adherent silicon dioxide (SiO2) film on gallium arsenide (GaAs) substrate by plasma enhanced chemical vapor deposition (PECVD) is proposed. Ar, N2, and NH3 were used as pre-treatment gas to improve the interfacial adhesion. The interfacial adhesion was measured by the cross-cut tape test. By the measurement of spectroscopic ellipsometry and x-ray photoelectron spectroscopy (XPS), it is revealed that nitrogen plasma pre-treatment had formed a very thin GaN transition layer on the surface, which was responsible for the improvement of interfacial adhesion. XPS depth-profiling further confirmed various pre-treatment gases generate plasma mixtures and form thin film layers with different compositions on the GaAs surface. These layers have a significant impact on the adhesion of the subsequently prepared SiO2 film. The primary mechanism for improving interfacial adhesion is the renovation of the substrate composition via plasma pre-treatment by PECVD, which forms a transition layer of nitrides that eliminates the negative effects of oxides on adhesion. This study reveals the mechanism of interfacial adhesion enhancement between SiO2 film and GaAs substrate, which is of significant importance in fabricating high-performance and reliable semiconductor devices.

Waterproof and ultraflexible organic photovoltaics with improved interface adhesion

Ultraflexible organic photovoltaics have emerged as a potential power source for wearable electronics owing to their stretchability and lightweight nature. However, waterproofing ultraflexible organic photovoltaics without compromising mechanical flexibility and conformability remains challenging. Here, we demonstrate waterproof and ultraflexible organic photovoltaics through the in-situ growth of a hole-transporting layer to strengthen interface adhesion between the active layer and anode. Specifically, a silver electrode is deposited directly on top of the active layers, followed by thermal annealing treatment. Compared with conventional sequentially-deposited hole-transporting layers, the in-situ grown hole-transporting layer exhibits higher thermodynamic adhesion between the active layers, resulting in better waterproofness. The fabricated 3 μm-thick organic photovoltaics retain 89% and 96% of their pristine performance after immersion in water for 4 h and 300 stretching/releasing cycles at 30% strain under water, respectively. Moreover, the ultraflexible devices withstand a machine-washing test with such a thin encapsulation layer, which has never been reported. Finally, we demonstrate the universality of the strategy for achieving waterproof solar cells.

Improvement of interfacial adhesion between oxide ceramic nanoparticles and epoxy resin by wet-jet milling

Although ceramic/polymer composites are useful for various applications, such as sensors, electronics, automobiles, and aerospace, the aggregation of nanoparticles can lead to the degradation of the mechanical and functional properties of the composites. To mitigate this, the interfacial adhesion between epoxy resin and the oxide ceramic nanoparticles γ-aluminum oxide (Al2O3), silicon dioxide, and magnesium oxide was strengthened by wet-jet milling (WJM) treatment without a chemical modifier. The WJM treatment of the slurry containing nanoparticles and epoxy resin led to the good adsorption of epoxy resin onto the nanoparticle surface, which significantly improved the mechanical properties of the composites. Throughout this process, the amount of epoxy resin adsorbed on the nanoparticle surface and the composite mechanical properties increased with increasing WJM processing pressure, owing to the increased contact between the nanoparticles and epoxy resin droplets and the reduced droplet size. Furthermore, poor solvent was found to be effective for the dispersal of the nanoparticles because the epoxy resin droplets in the slurry were more stable on the nanoparticle surfaces than those in the solvent. When Al2O3 nanoparticles were used as a filler, the amount of epoxy resin adsorbed increased from 3.7 to 70.6 mg g−1, and the composite tensile strength increased from 67.1 to 100.3 MPa in poor solvent and under high WJM processing pressure. This optimized WJM treatment will lead to improvements in the mechanical and functional properties of various composite materials.

Core-shell ZrO2@GO hybrid for effective interfacial adhesion improvement of carbon fiber/epoxy composites

A core-shell structured ZrO2@GO hybrid was fabricated and incorporated onto carbon fiber via dip-coating for the first time for effectively enhancing the interfacial adhesion of epoxy composites. ZrO2@GO functionalized fiber composite exhibits the optimal interfacial shear strength, with 47.5%, 21.8% and 16.8% augmentations over that of untreated fiber, only epoxy sizing coated fiber and silane coupling agent-encapsulated ZrO2 decorated fiber composites, suggesting that GO could serve as a new coupling agent for enhancing the affinity of inorganic nanoparticles with resin component instead of the traditional silane coupling agent. The reinforcing mechanisms are ascribed to the improved resin wettability, abundant functional groups offered by GO for increasing multiple interactions with epoxy resin and the formation of a mobile network absorbing energy. It is believed that the core-shell ZrO2@GO structure, with inner rigid particles and outer flexible coupling agent, can fully utilize the synergistic enhancement effect of different components and provide new insights into designing nano-structured interphase for the improvement in interfacial adhesion of fiber-polymer composites.

Functionalization of various coffee husk biofibers on the rheological and thermomechanical properties of poly(butylene succinate)-urethane blended composites

Many studies have reported that surface-functionalized biofibers originating from plant waste can be used to improve the compatibility and processability of polymer blend systems. This study investigated the effects of size distribution and surface treatment of coffee husk (CH) biofibers on the rheological and thermomechanical properties of poly(butylene succinate)/thermoplastic polyurethane polymer blend composite. CH is a coffee waste with interlinked complex macromolecular structure of lignocellulose materials like cellulose, hemicellulose, and lignin. It was found that the handling and processability of the composites improved after the CH was surface-functionalized with diisocyanate/methacrylate prior to composite fabrication. Smaller-sized surface-treated CHs showed superior processability owing to the entanglement of fibers through the matrices associated with the improvement of interfacial adhesion. Therefore, the frequency-dependent rheological test revealed an increase in complex viscosity and storage modulus with the surface treatment and size reduction of CHs. Regardless of the size distribution, the degree of crystallinity of poly(butylene succinate) in the composites filled with surface-treated CHs reduced by about 20%. The composites with treated CHs also demonstrated superior thermal stability than their corresponding composites with raw CHs.

An Adhesion Improvement of Low-Density Polyethylene to Aluminum through Modification with Functionalized Polymers.

An interfacial adhesion improvement between low-density polyethylene (LDPE) and aluminum (Al) foil is an important challenge in designing multilayered packaging (TetraPak packaging type) due to insufficient inherent adhesion between both untreated materials. Therefore, extra adhesive layers are often used. The hydrophobic character of LDPE is responsible for poor adhesion to Al and can result in delamination. This study deals with the comparative study of the bulk modification of LDPE with various commercially available adhesive promoters with different chemical compositions to increase LDPE's adhesive characteristics and ensure good adhesion in LDPE/Al laminates. A copolymer of ethylene and methacrylic acid; a terpolymer of ethylene, maleic anhydride, and acrylic ester; or maleated polyethylene (PE) were used as adhesive promoters, and their effect on adhesion improvement of LDPE to Al was investigated. The best adhesion improvement was observed in LDPE-modified samples with maleated PE, while 0.1 wt.% additive content significantly increased peel resistance (from zero to 105 N/m). An additional increase in additive content (0.5 wt.%) in LDPE led to stronger adhesion forces than the cohesion forces in Al foil. Adding 0.5 wt.% of maleated PE into LDPE improved the LDPE/Al laminates' adhesion and can be applied in multilayered lamination applications.

Strengthening and Toughening Epoxy Composites by Constructing MOF/CF Multi-Scale Reinforcement

The interfacial designing of carbon fiber (CF)/epoxy composites, as a well-accepted method used to obtain high-performance composites, has gained extensive attention. However, an improvement in interfacial adhesion is usually accompanied by a simultaneous decrease in toughness, which has become an obstacle to the performance enhancement of CF/epoxy composites. Herein, nanosized UiO-66-NH2 was proposed to yield on the CF surface through an in situ growth method for preparing high-performance CF/epoxy composites. The induced UiO-66-NH2 could significantly enhance the active groups, surface roughness and wettability on the fiber surface, which can be confirmed by XPS, FTIR, dynamic contact angle (DCA) and SEM. Moreover, the porous structure of UiO-66-NH2 enables the epoxy resin to pass through it, which could toughen the matrix by forming an interpenetrating network structure and reducing the density of resin crosslinking. Meanwhile, the size effect of UiO-66-NH2 could hinder the crack propagation and release the stress concentration. Benefiting from these interfacial strengthening and toughening effects, the interlaminar shear strength and impact strength increased by 44.2% and 27.6%, respectively, in comparison to those of untreated CF. This work proposes a simple and effective strategy for interfacial designing that could offer new ideas for solving the conflict between the strengthening and toughening and provide a practical basis for preparing high-performance resin matrix composites.

Improvement of interfacial adhesion of CuO nanostructured carbon fiber reinforced polymer composites

AbstractHydrothermal technique was used to deposit copper‐oxide (CuO) nanostructures on woven carbon fibers (WCF) to produce a nanostructured interphase that increased the interfacial strength with an epoxy resin matrix. In order to create laminated hybrid composites, CuO‐modified WCF was reinforced with mixture of bisphenol‐A epoxy resin and dimethyl aniline hardener as matrix using the vacuum bagging approach. Enhanced mechanical qualities are the result of increased volume fraction of CuO nanostructures, where the void content is minimal. The mechanical characteristics such as impact strength and tensile strength of CuO‐coated WCF reinforced epoxy resin composite samples were assessed using drop‐down impact test and universal material testing system. The outcomes demonstrate a considerable improvement in impact energy absorption (74.8%), elastic modulus (52%) tensile strength (42%) and in‐plane shear strength (32%) for the CuO‐coated WCF reinforced epoxy resin composites. This work demonstrates that the development of CuO nanostructures can lessen composite delamination and enhance composite performance because of the increase in interfacial surface area between the matrix and the fiber by CuO nanostructures potentially expanding the spectrum of structural applications for these materials.

Effects of polycarbonate crystals, π-π interactions, and chemical bonds at an interface on the interfacial adhesion between polycarbonate and reinforcing fibers

The effects of polycarbonate (PC) crystals and physical and chemical interactions at the interface on the interfacial adhesion between PC and reinforcing fibers were explored. Carbon fibers (CFs) and glass fibers (GFs) with different surface functional groups were prepared as reinforcing fibers. The specimens were prepared by compositing each reinforcing fiber type with PC dissolved in tetrahydrofuran, and the interfacial adhesion was evaluated using a microdroplet test after annealing the samples at various temperatures. The Raman spectra of PC near the reinforcing fibers, molecular weight, and electron spin resonance (ESR) of PC were investigated. The results demonstrate that the π−π interactions between PC and CFs and the chemical interaction between the radicals generated in PC and the functional groups on the CF surface play key roles in the improvement of interfacial adhesion. Specifically, the detection of PC radicals by ESR, shown herein, is essential for understanding the chemical interactions.

Improvement of Interfacial Adhesion and Thermomechanical Properties of PLA Based Composites with Wheat/Rice Bran

The present work aims to enhance the use of agricultural byproducts for the production of bio-composites by melt extrusion. It is well known that in the production of such bio-composites, the weak point is the filler-matrix interface, for this reason the adhesion between a polylactic acid (PLA)/poly(butylene succinate)(PBSA) blend and rice and wheat bran platelets was enhanced by a treatment method applied on the fillers using a suitable beeswax. Moreover, the coupling action of beeswax and inorganic fillers (such as talc and calcium carbonate) were investigated to improve the thermo-mechanical properties of the final composites. Through rheological (MFI), morphological (SEM), thermal (TGA, DSC), mechanical (Tensile, Impact), thermomechanical (HDT) characterizations and the application of analytical models, the optimum among the tested formulations was then selected.

Two-dimensional polydopamine nano-protrusion-modified graphene oxide encapsulation of cylindrical carbon fiber by vacuum filtration to strengthen the interphase of epoxy composites

Interfacial delamination is an everlasting problem that exists in carbon fiber reinforced polymer composites and restricts their ability to undertake greater shear load. Herein, vacuum filtration technique is first successfully utilized to realize the functionalization of cylindrical carbon fiber by two-dimensional graphene oxide (GO) and polydopamine nano-protrusions modified GO (GOPDA) as a rapid, simple and versatile means to realize the improvement of interfacial adhesion of epoxy composites. Compared to the GO modifier (37.6% augmentation), the GOPDA addition results in higher gain in interfacial shear strength (68.4%) over that of de-sized fiber. This belongs to that the adherence of smaller-sized GOPDA and its nano-protrusion structure facilitate the high surface energy, excellent wetting, mechanical interlocking and covalent linking with epoxy resin. Our research highlights the great possibility to implement vacuum filtration to modify the traditional circumferential fiber and realize the interphase optimization of composites.

Novel compatibilizers and plasticizers developed from epoxidized and maleinized chia oil in composites based on PLA and chia seed flour

Novel compatibilizers and plasticizers derived from epoxidized chia seed oil (ECO) and maleinized chia seed oil (MCO) have been applied in composites based on poly(lactic acid) (PLA) and 15 wt% chia seed flour (CSF). Results obtained have been compared to conventional silane coupling agent, (3-glycidyloxypropyl) trimethoxysilane (GPS), and a petroleum-based compatibilizer, poly(styrene-co-glycidyl methacrylate) copolymer (Xibond, ®). The compatibilization effect of green composites were assessed by FTIR. The addition of all four compatibilizers improved the ductile mechanical and thermal properties of the composites. The morphology analysis revealed an improvement of interfacial adhesion of the CSF particles into the PLA matrix. In particular, ECO and MCO composites showed a roughness with long filaments in their morphology which plays a crucial role in improving the ductile properties highly. The elongation at break was 10 and 8 times higher using ECO and MCO, respectively, compared to uncompatibilized composite. Moreover, the composites manufactured showed low values (<9%) in the water uptake assay and a negligible compostability delay. The use of novel compatibilizers based on modified vegetable oils could mean an interesting proposal to obtain an entirely environmentally friendly composite with a remarkable ductile property.