Acrylonitrile Copolymer Research Articles

Achieving optimum balance between mechanical properties and gloss of acrylonitrile–styrene–acrylate resin through control of rubber particle size distribution

AbstractPreparation of acrylonitrile–styrene–acrylate (ASA) with high gloss and superior impact properties is still challenging. Here, we developed a new strategy for the preparation of ASA resins by a selective redox initiation method based on a semi‐continuous emulsion polymerization technique. A series of ASA core‐shell impact modifiers were firstly obtained by grafting styrene (St) and acrylonitrile (AN) onto poly(n‐butyl acrylate) (PBA) seeded latexes of different sizes. The ASA core‐shell impact modifier was then used to toughen the styrene–acrylonitrile copolymer (SAN). The synergistic effects between the single particle size of the rubber phase and different particle sizes were systematically investigated, and the mechanical properties of SAN‐toughened resins at various particle sizes of the rubber phase were analyzed. The results revealed that toughened SAN with small particle sizes possessed better gloss, and the impact strength of the doped small‐particle toughened SAN was much higher than that of the single particle size toughened SAN. The ASA graft powders synthesized from large particle PBA (particle size 316 nm) and small particle PBA (particle size 99 nm), respectively, were mixed at a 50/50 ratio and blended with SAN resin, a gloss level reaching 95, and an impact performance of 275 J/m values almost twice those of a single particle size toughened SAN.Highlights Acrylonitrile–styrene–acrylate resins with an impact strength of 275 J/m and gloss of 95 were prepared. The balance between mechanical properties and gloss of acrylonitrile–styrene–acrylate resin was obtained. Polymerization was initiated at low temperature.

In Situ Formation of Acidic Comonomer during Thermal Treatment of Copolymers of Acrylonitrile and Its Influence on the Cyclization Reaction.

Binary and ternary copolymers of acrylonitrile (AN), tert-butyl acrylate (TBA), and n-butyl acrylate (BA) are synthesized through conventional radical polymerization in DMSO in the presence of 2-mercaptoethanol. The thermal behavior of binary and ternary copolymers is studied under argon atmosphere and in air. It is demonstrated that the copolymers of AN contain 1-10 mol.% of TBA split isobutylene upon heating above 160 °C, resulting in the formation of the units of acrylic acid in the chain. The carboxylic groups formed in situ are responsible for the ionic mechanism of cyclization, which starts at lower temperatures compared with pure polyacrylonitrile (PAN) or AN copolymer with BA. The activation energy of cyclization through ionic and radical mechanisms depends on copolymer composition. For the ionic mechanism, the activation energy lies in the range ca. 100-130 kJ/mole, while for the radical mechanism, it lies in the range ca. 150-190 kJ/mole. The increase in the TBA molar part in the copolymer is followed by faster consumption of nitrile groups and the evolution of a ladder structure in both binary and ternary copolymers. Thus, the incorporation of a certain amount of TBA in PAN or its copolymer with BA allows tuning the temperature range of cyclization. This feature seems attractive for applications in the production of melt-spun PAN by choosing the appropriate copolymer composition and heating mode.

Compatibilizing and toughening of the styrene and acrylonitrile copolymer and core‐shell impact modifier obtained by agglomerate technologies

AbstractParticle size distribution and the compatibility of core‐shell impact modifiers play a crucial role in determining the mechanical properties of the resin. This study presents the synthesis of a core‐shell impact modifier, a copolymer of polybutadiene grafted with styrene and acrylonitrile (PBL‐g‐SAN), using emulsion polymerization to enhance the mechanical properties of SAN resin. Polymer agglomeration technologies were employed to increase the particle size of polybutadiene latex, resulting in particles approximately 300 nm in diameter. Moreover, the effects of core‐shell modifiers with different constitutions on the mechanical properties of ABS resin were investigated. By optimizing the grafting polymerization process, improvements in impact strength of ABS resin were observed. When the St/AN ratio of the core‐shell modifier is 75/25, with a core‐shell ratio of 60/40 and MMA content at 2.5%, the impact strength of ABS resin reaches its peak while maintaining high tensile strength. The incorporation of methyl methacrylate improved the dispersion of core‐shell modifiers in SAN resin. Compared to commercial ABS resins with the same SAN and rubber content, the modified resin demonstrated a nearly 20% improvement in impact performance, and significant reductions in both production time and costs due to the polymer agglomeration method.Highlights The 300 nm polybutadiene latex was synthesized by polymer agglomeration technology. The relationship between the composition of these core‐shell modifiers and the mechanical properties of ABS resin was explored. The ABS resin with impact strength exceeding 20% of commercial material is prepared.

Numerical Studies of Solid Rocket Propellant PMMA-PBAN-ALF3-Nitrocellulose-Difluoramine

Abstract The aim of the new investigation is the evaluation of solid rocket Propellant. In which performing numerical analysis of solid rocket propellant and calculating the constraints involved as derived from thrust i.e. velocity involved in the solid rocket propulsion motor usage. This paper aims to show the viability of solid rocket propellant for modern and future applications. Solid rocket motors are simple in design and fabricating. The need for a propellant that produces the same specific impulse as another chemical rocket engine. So it is needed to have a solid rocket motor with an enhanced combustion characteristic at a reasonable O/F ratio. For a healthy ecology, an economically reliable, highly effective, and environmentally concerned propellant is constantly suitable. As a superior alternative among the already used propellants in the sector, the paper suggested fuel PolyMethyl MethAcrylate (PMMA), PolyButadiene AcryloNitrile (PBAN) CoPolymer, and Aluminum hydride (AlH3), and oxidizers such as Nitrocellulose and Difluoramine. The desired O/F ratio for the technical criteria was found to result in a high combustion characteristic. With the features discovered through numerical and analytical research, we have suggested a design for the SRM that includes post-combustion, which enhances the reaction and creates the innovative elements of the existing SRM.

FFF/FDM 3D-Printed Solid Polymer Electrolytes Based on Acrylonitrile Copolymers for Lithium-Ion Batteries.

Lithium-ion batteries (LIBs) are essential in modern electronics, particularly in portable devices and electric vehicles. However, the limited design flexibility of current battery shapes constrains the development of custom-sized power sources for advanced applications like wearable electronics and medical devices. Additive manufacturing (AM), specifically Fused Filament Fabrication (FFF), presents a promising solution by enabling the creation of batteries with customized shapes. This study explores the use of novel poly(acrylonitrile-co-polyethylene glycol methyl ether acrylate) (poly(AN-co-PEGMEA)) copolymers as solid polymer electrolytes for lithium-ion batteries, optimized for 3D printing using FFF. The copolymers were synthesized with varying AN:PEGMEA ratios, and their physical, thermal, and electrochemical properties were systematically characterized. The study found that a poly(AN-co-PEGMEA) 6:1 copolymer ratio offers an optimal balance between printability and ionic conductivity. The successful extrusion of filaments and subsequent 3D printing of complex shapes demonstrate the potential of these materials for next-generation battery designs. The addition of succinonitrile (SCN) as a plasticizer significantly improved ionic conductivity and lithium cation transference numbers, making these copolymers viable for practical applications. This work highlights the potential of combining polymer chemistry with additive manufacturing to provide new opportunities in lithium-ion battery design and function.

Fabrication of Flexible Wearable Mechanosensors Utilizing Piezoelectric Hydrogels Mechanically Enhanced by Dipole-Dipole Interactions.

Conductive hydrogels have been increasingly employed to construct wearable mechanosensors due to their excellent mechanical flexibility close to that of soft tissues. In this work, piezoelectric hydrogels are prepared through free radical copolymerization of acrylamide (AM) and acrylonitrile (AN) and further utilized in assembling flexible wearable mechanosensors. Introduction of the polyacrylonitrile (PAN) component in the copolymers endows the hydrogels with excellent piezoelectric properties. Meanwhile, significant enhancement of mechanical properties has been accessed by forming dipole-dipole interactions, which results in a tensile strength of 0.51 MPa. Flexible wearable mechanosensors are fabricated by utilizing piezoelectric hydrogels as key signal converting materials. Self-powered piezoelectric pressure sensors are assembled with a sensitivity (S) of 0.2 V kPa-1. Additionally, resistive strain sensors (gauge factor (GF): 0.84, strain range: 0-250%) and capacitive pressure sensors (S: 0.23 kPa-1, pressure range: 0-8 kPa) are fabricated by utilizing such hydrogels. These flexible wearable mechanosensors can monitor diverse body movements such as joint bending, walking, running, and stair climbing. This work is anticipated to offer promising soft materials for efficient mechanical-to-electrical signal conversion and provides new insights into the development of various wearable mechanosensors.

Preparation of Poly(Styrene-co-Acrylonitrile)-Grafted Attapulgite via Simultaneous Reverse and Normal Initiation Atom Transfer Radical Polymerization (SR&NI ATRP) and Its Effect on Polycarbonate/Acrylonitrile-Butadiene-Styrene Terpolymer Ternary Composites

To further improve the comprehensive properties of polycarbonate/acrylonitrile–butadiene–styrene terpolymer blends (PC/ABS), in this work, styrene–acrylonitrile copolymer [P(St-co-An)] was grafted on the surface of attapulgite particles (ATP) by simultaneous reverse and normal initiation ATRP (SR&NI ATRP) to yield ATP@P(St-co-An) hybrid particles. Then a series of PC/ABS/ATP@P(St-co-An) composites were prepared via the melt blending method. The effects of ATP@P(St-co-An) content on the morphological, mechanical, thermal and rheological properties of the composites were investigated in detail. The core-shell ATP@P(St-co-An) hybrid particles with the polymer layer thickness of 20-40 nm were synthesized successfully according to the results of X-ray photoelectron spectrometer (XPS), Fourier transform infrared spectrometer (FTIR), gel permeation chromatography (GPC), thermogravimetric analysis (TGA) and transmission electron microscopy (TEM). The improvement in mechanical properties, reduced glass transition temperature (T g) difference between PC and ABS and micromorphology changes of the composites proved the compatibilization, strengthening, and toughening effect of the ATP@P(St-co-An). Compared with the PC/ABS blend, with strength and toughness of 50.8 MPa and 56.3 kJ/m2, when the ATP@P(St-co-An) content was 4 wt%, a reasonable balance (85.8 MPa and 86.2 kJ/m2) between strength and toughness was achieved with substantially enhanced thermal stability. Moreover, the composite showed more remarkable non-Newtonian behavior, and its processability was also improved. We believe this work provides an effective approach to optimize the compatibility and comprehensive properties of PC/ABS blends.

Structural Rheology in the Development and Study of Complex Polymer Materials.

The progress in polymer science and nanotechnology yields new colloidal and macromolecular objects and their combinations, which can be defined as complex polymer materials. The complexity may include a complicated composition and architecture of macromolecular chains, specific intermolecular interactions, an unusual phase behavior, and a structure of a multi-component polymer-containing material. Determination of a relation between the structure of a complex material, the structure and properties of its constituent elements, and the rheological properties of the material as a whole is the subject of structural rheology-a valuable tool for the development and study of novel materials. This work summarizes the author's structural-rheological studies of complex polymer materials for determining the conditions and rheo-manifestations of their micro- and nanostructuring. The complicated chemical composition of macromolecular chains and its role in polymer structuring via block segregation and cooperative hydrogen bonds in melt and solutions is considered using tri- and multiblock styrene/isoprene and vinyl acetate/vinyl alcohol copolymers. Specific molecular interactions are analyzed in solutions of cellulose; its acetate butyrate; a gelatin/carrageenan combination; and different acrylonitrile, oxadiazole, and benzimidazole copolymers. A homogeneous structuring may result from a conformational transition, a mesophase formation, or a macromolecular association caused by a complex chain composition or specific inter- and supramolecular interactions, which, however, may be masked by macromolecular entanglements when determining a rheological behavior. A heterogeneous structure formation implies a microscopic phase separation upon non-solvent addition, temperature change, or intense shear up to a macroscopic decomposition. Specific polymer/particle interactions have been examined using polyethylene oxide solutions, polyisobutylene melts, and cellulose gels containing solid particles of different nature, demonstrating the competition of macromolecular entanglements, interparticle interactions, and adsorption polymer/particle bonds in governing the rheological properties. Complex chain architecture has been considered using long-chain branched polybutylene-adipate-terephthalate and polyethylene melts, cross-linked sodium hyaluronate hydrogels, asphaltene solutions, and linear/highly-branched polydimethylsiloxane blends, showing that branching raises the viscosity and elasticity and can result in limited miscibility with linear isomonomer chains. Finally, some examples of composite adhesives, membranes, and greases as structured polymeric functional materials have been presented with the demonstration of the relation between their rheological and performance properties.

Preparation of poly(butyl acrylate)‐grafted‐poly(styrene‐co‐acrylonitrile) particles for toughening poly(styrene‐co‐acrylonitrile) resin

AbstractHerein, the impact modifier of poly(butyl acrylate) grafted poly(styrene‐co‐acrylonitrile) (PBA‐g‐SAN) with 60% rubber content was prepared by emulsion grafting polymerization and subsequently blended with styrene–acrylonitrile copolymer (SAN) resin to construct acrylate styrene acrylonitrile (ASA) resins. The effects of acrylonitrile content of PBA‐g‐SAN copolymer and PBA size on the ASA resins' mechanical properties were investigated. Experimental results revealed that ASA resin's highest impact strength reached 27.75 kJ/m2. The lap shear adhesion test suggested that the PBA‐g‐SAN copolymer with 21% AN content exhibited excellent interfacial adhesion with SAN resin. The PBA‐g‐SAN particles with 100 and 400 nm poly (butyl acrylate) as core rubbers demonstrated a synergistic toughening effect for SAN resin. The high blackness ASA resin with excellent impact resistance was obtained when the 100 nm and the 400 nm poly (butyl acrylate) particle mass ratio reached 8/2.Highlights The ASA resin with 27.75KJ/m2 impact strength was prepared. The synergistic toughening mechanisms were investigated. The high blackness ASA resin was constructed.

Modeling Rinsing of Residual Solvent from Fiber Produced from the Copolymer of Acrylonitrile, Methacrylate, and 2-Acrylamide-2-Methylpropanesulfonic Acid

Modeling Rinsing of Residual Solvent from Fiber Produced from the Copolymer of Acrylonitrile, Methacrylate, and 2-Acrylamide-2-Methylpropanesulfonic Acid

Določanje obstojnosti funkcionaliziranih tekstilij na osnovi kopolimerov akrilonitrila na toplotno in toplotno-oksidativno razgradnjo

Acrylonitrile is widely used to produce carbon fibres, household textiles, artificial fur, etc. The modification of polyacrylonitrile fibres in an alkaline medium is extended in the production of textile sorbents. The scientific direction of fibre modification through surface activation using hydrogen peroxide is of scientific interest. However, the thermal and thermophysical properties of the samples are not examined. Therefore, interest arises when analysing the effect of polyacrylonitrile textile material functionalization on the resistance of fibres to thermal oxidation and thermal degradation. The study of thermogravimetry and differential thermogravimetry thermooxide of polyacrylonitrile – modified fibres is carried out using thermogravimetric analysis to research the thermal oxidation and thermal degradation of modified polyacrylonitrile fibre samples. A change in the rate of thermal oxidative-degradation in the process of functionalization was identified in this research. A change in the loss of mass of the sample under different conditions of functionalization was also identified. The total glass transition of the polyacrylonitrile was achieved by heating the polymer to 130 °C. The intensification self-regulation of the structure of the polymeric material through the formation of the mesophase was released at the temperature of around 100 °C. During the heating of the initial polyacrylonitrile textile material to the temperature of 70‒80 °C, a weakening of intermolecular contacts was observed, which led to an increase in the mobility of macromolecular segments. The temperature of 78 °С was considered to be the initial glass transition temperature Tg,t1 and Tg,t2 – 121 °С as the final temperature for the original sample. However, if the temperature exceeded 130 °C, chemical changes in the polymer occurred, in particular, the process of cyclization. The analysis of the thermogravimetry data of thermally oxidized samples resulted in the retention of the complex stepwise nature of decomposition inherent in the initial fibrous material based on acrylonitrile copolymers. The conducted analysis showed the absence of significant changes in the reasonable conditions of chemical modification and practical operation of textile materials. The physical and mechanical properties of functionalized textile materials based on acrylonitrile copolymers were studied. As a result of surface functionalization, an insignificant strength reduction of functionalized textile materials occurred.

Synthesis and Properties of Vinyl Ether and Acrylonitrile Copolymers

AbstractThe radical copolymerizations of vinyl ethers, including ethylene glycol monovinyl ether (HEVE) and isobutyl vinyl ether (IBVE), and acrylonitrile (AN) are investigated. The reactivity ratios of comonomers are evaluated by Fineman–Ross (rHEVE = 0.032 and rAN = 1.054, and rIBVE = 0.031 and rAN = 13.984) and Kelen–Tudos (rHEVE = 0.001 and rAN = 1.036, and rIBVE = 0.032 and rAN = 13.981) methods, respectively. The conversions of HEVE and IBVE under similar conditions also support that HEVE has a higher reactivity than that of IBVE. A series of poly(HEVE‐co‐AN)s (Mn from 56 000 to 110 000) and poly(IBVE‐co‐AN)s (Mn from 52 000 to 97 000) with random sequential structure are prepared. Furthermore, the glass transitional temperatures of poly(vinyl ether‐co‐AN)s decrease with the increase of vinyl ether units in the copolymers. Thermal stability of poly(vinyl ether‐co‐AN)s is comparable, which is slightly affected by vinyl ether contents. Poly(HEVE‐co‐AN)s possess a two‐stage weight loss (one around 230 °C, and the other around 300 °C), and poly(IBVE‐co‐AN)s decompose at around 350 °C with one stage. In addition, the poly(HEVE‐co‐AN)s demonstrate a good hydrophilicity of which the average of static water contact angles decrease from 85.4° to 62.4° with the HEVE units increased from 8% to 33%.

Enhancing oil–water emulsion separation using improved styrene–acrylonitrile copolymer membrane: Experimental and thermodynamic study of the impact of solvent mixtures

AbstractThis study investigated the fabrication of styrene–acrylonitrile copolymer (SAN) membrane using the nonsolvent‐induced phase separation (NIPS) method with a combination of solvents, namely N‐methyl‐2‐pyrrolidone (NMP) and dimethylformamide (DMF) and water as the nonsolvent. Since the impact of varying solvent ratios on SAN membrane performance remained unexplored, this study aimed to address this knowledge gap in the context of oil–water emulsion separation. Experimental results demonstrated that employing a solvent mixture, rather than a pure solvent, led to improved membrane performance. The primary objective of this work was to experimentally determine the optimal solvent ratio for enhancing SAN copolymer membrane performance. Additionally, the Flory–Huggins thermodynamic model was applied to investigate the possibility of predicting membrane binodal data. The thermodynamic analysis revealed a strong agreement between calculated and experimental binodal data, with an error of less than 3.8%. Notably, membranes produced with an equal solvent ratio exhibited the most hydrophilic properties, resulting in increased permeability. The permeate flux for distilled water reached 320 L/(m2 h) (LMH), and water contact angle of the membrane was 22°. Furthermore, mechanical resistance increased up to 50%. These results highlight the promising potential of fabricating SAN membrane using solvent mixtures for oil–water emulsion separation.

Quantification of natural rubber blends by reflection/reflectance infrared and confocal Raman spectroscopy: a comparison of statistical methods.

The blend of butadiene and acrylonitrile copolymer (NBR) with natural poly-cis-isoprene (NR) shows increased resistance to swelling in solvents in comparison to the individual components. In aerospace, NBR rubber is used as thermal protection for rockets and shall not contain other polymers, even in low contents, otherwise, it can affect the protection performance and rocket safety by causing detachment of the elastomer/propellant interface; therefore, this investigation presents methodologies to determine the NR/NBR contents. This study explores different analytical techniques, such as Raman spectroscopy and Fourier transform infrared (FTIR) spectroscopy, in the mid-infrared (MIR) by reflection and in the near-infrared by reflectance (NIRA) modes, Furthermore, quantification strategies by univariate, bivariate and multivariate (chemometric) models are evaluated and compared. A proposed methodology, based on multivariate Raman microscopy with partial least squares regression (PLS), showed high linearity (R2 > 0.99) and low error (< 0.82 %). The validation of FT-MIR data for the CH3, which presented lower error (1.3%) than vinylidene band (6%), showed that both methodologies (reflection and NIRA reflectance) can be used for the quantification of NR in NR/NBR. These results constitute a contribution to the state of the art in researching industrial and aerospace elastomeric applications.

Self-adhesion of uncrosslinked poly(butadiene-co-acrylonitrile), i.e. nitrile rubber, an inhomogeneous and associative polymer.

Nitrile rubber (i.e., NBR) is a crosslinked copolymer of butadiene and acrylonitrile that finds widespread use in the automotive and aerospace industry as it sustains large, reversible deformations while resisting swelling by petrochemical fuels. We recently demonstrated that this material has a drift in composition due to the difference in reactivity between acrylonitrile and butadiene monomers during emulsion copolymerisation. Thus, although NBR is often thought of as a random copolymer, it does experience thermodynamic driving forces for self-assembly and kinetic barriers for processing like those of block copolymers.1 Here, we illustrate how such drift in composition hinders interdiffusion and prevents self-adhesion. The key result is that contacting uncrosslinked NBR (i) in the melt, (ii) in the presence of tackifiers, or (iii) in the presence of organic solvents promotes interdiffusion and enables self-adhesion. However, the contact times required for self-adhering, tc ∼ O(100 h), are orders of magnitude above those needed for non-polar synthetic rubbers like styrene-butadiene rubber (i.e., SBR) of comparable molecular weights and glass transition temperatures, tc ∼ O(100 s), unveiling the dramatic effect of compositional inhomogeneities and physical associations on polymer interdiffusion and large-strain mechanical properties. For example, when welded with organic solvents, the self-adhesion energy of NBR continues to increase after the solvent has evaporated because of polymer nanostructuring.

A new granulated sorbent based on acrylonitrile: Synthesis and physico-chemical properties

It was common practice in water treatment procedures to employ functional polymers to sorb metallic species from the water. Due to the wide spectrum of potential functional groups on polymeric backbones, these sorbents had the potential to separate a huge range of metals. The characteristics of the cationic metallic ions and the functional groups were closely related to the selectivity and sorption efficiency via complexation or ion exchange interactions. Another crucial factor that needed to be taken into account was the physical makeup of the materials. Major variations in sorption characteristics were found in the sorption kinetics, which were contingent on the cross-linking density, polymer solubility and polymeric architecture. An anion-exchange and complexing property-rich novel granular sorbent was created by the chemical reaction of a cross-linked copolymer of acrylonitrile with hexahydro-1,3,5-triacrylyltriazine when subjected to hydroxylamine. Modern techniques have been used to examine the physico-chemical characteristics of the final sorbent and demonstrate the characteristics of its structural morphology.

Acrylonitrile‐styrene‐acrylate particles with different acrylonitrile contents for improving the toughness of poly(vinyl chloride) resin

AbstractPoly(butyl acrylate) grafted styrene and acrylonitrile copolymer (PBA‐g‐SAN, ASA) with core–shell structures were prepared by emulsion polymerization technology to improve the toughness of the poly(vinyl chloride) (PVC). The mechanical properties of the PVC/ASA blends were investigated. The notch impact strength of the PVC/ASA blend could reach 1200 J/m when the 13 phr ASA was added to the PVC. This was several times more than pure PVC resin. Scanning electron microscopy analysis results indicated that the improvement in impact strength of the PVC/ASA blend was attributed to shear yielding induced by ASA particles. Additionally, subtle changes in the ratio of monomers in the shell layer led to significant fluctuations in the mechanical properties of the composites. Dynamic mechanical analysis showed that the intermolecular interaction forces between ASA particles and PVC resins played a key role in improving the toughness of PVC/ASA blend.

Tuning the distribution of carbon nanotubes in styrene–acrylonitrile copolymer by a small amount of polycarbonate

Tuning the distribution of carbon nanotubes in styrene–acrylonitrile copolymer by a small amount of polycarbonate

Preparation of a Structural Polyimide Foam Plastic Based on a Bulk Copolymer of Acrylonitrile and Methacrylic Acid

Foaming of particles of acrylonitrile–methacrylic acid copolymer in the temperature interval 160–220°С was studied. As shown by IR spectroscopy, the final polymer matrix of the foam plastics consists of glutarimide fragments. Thermogravimetric analysis shows that the products start to degrade at a high temperature (about 350°С). The effect of the prolonged heat treatment at 150–190°С on the physicomechanical characteristics of the foamed plastics was examined.

Effect of Functionalized Liquid Rubber on Mechanical Properties of an Epoxy Resin

AbstractIn this study, an epoxy resin has been modified with different weight ratios of carboxyl‐terminated polybutadiene liquid rubber. The introduction of a pre‐reaction catalyst has been necessary to promote the reaction between the epoxy groups and the carboxylic acid groups of carboxyl‐terminated butadiene acrylonitrile copolymer. The occurred reaction has been confirmed by infrared spectroscopy analysis. The analysis of the mechanical properties has shown that the presence of elastomeric domains allows obtaining a matrix with greater flexibility. This allows making the material competitive for many applications such as adhesives and composite matrices where a high fracture toughness is required.