Sugarcane Bagasse-Derived Activated Carbon- (AC-) Epoxy Vitrimer Biocomposite: Thermomechanical and Self-Healing Performance

Vitrimeric materials have emerged as fascinating and sustainable materials owing to their malleability, reprocessability, and recyclability. Sustainable vitrimeric materials can be prepared by reinforcing polymeric matrix with bioderived fillers. In the current work, a sustainable vitrimer is prepared by incorporating biomass-derived activated carbon (AC) filler into the epoxy matrix to achieve enhanced thermal and mechanical properties. Thus, prepared biocomposite vitrimers demonstrate a lower-temperature self-healing (70°C for 5 min) via disulfide exchanges, compared to the pristine epoxy vitrimers (80°C for 5 min). Significantly, the self-healing performances have been studied extensively with the flexural studies; and changes in material healing efficiency have been demonstrated based on the observed changes in modulus

An Overview on Carbon Fiber-Reinforced Epoxy Composites: Effect of Graphene Oxide Incorporation on Composites Performance

Carbon fiber-reinforced polymer (CFRP) composites are used in a variety of applications such as aircraft, automobiles, body armors, and the sports sector owing to their ultra-strong and lightweight characteristics. However, the incorporation of an untreated pristine carbon fiber surface leads to a weak interfacial interaction with the polymeric matrix, thus triggering catastrophic failure of the composite material. Graphene oxide, a 2D-macromolecule consisting of several polar functional groups such as hydroxyl, carboxyl, and carbonyl on the basal planes and edges, tends to increase the surface area and has thus been applied between the fiber and matrix, helping to improve CFRP properties. Herein, we condense different routes of functionalization of GO nanosheets and their incorporation onto a fiber surface or in a carbon fiber-reinforced epoxy matrix, helping to improve the interfacial adhesion between the fiber and matrix, and thus allowing effective stress transfer and energy absorption. The improvement of the interfacial adhesion between the fiber and carbon fiber-reinforced epoxy matrix is due to the peculiar structure of GO nanoparticles composed of polar groups, especially on the edges of the nanosheets, able to provide strong interaction with the hosting cured epoxy matrix, and the “core” part similar to the structure of CFs, and hence able to establish strong π-π interactions with the reinforcing CFs. The article also covers the effect of functionalized graphene oxide incorporation on the mechanical, thermal, electrical, and viscoelastic properties of composite materials reinforced with carbon fibers

Self-healing epoxy/PDMS/graphene oxide nanocomposites for anti-corrosive applications

This study discusses the synthesis, characterization and development of self-healing nanocomposite of amino-terminated PDMS (Polydimethylsiloxane), Epoxy (EPON828 ̧ Diethylenetriamine (DETA)), and Graphene Oxide (GO). GO was prepared using a modified Hummer’s method and was incorporated into the PDMS-Epoxy composite in various ratios (0.1 wt.%, 0.3 wt.%, and 0.5 wt.%) using toluene as the dispersing medium. Fourier Transform Infrared Spectroscopy was used for confirming the presence of the designed/prepared structures, and thermo-mechanical analysis was performed to test the change in glass transition temperature and initiation temperature of self-healing process. The composite resins were coated on mild steel substrates by curing freshly prepared resins over the substrates at elevated temperatures. The corrosion behavior of mild steel in 3.5 wt.% NaCl solution before and after the coatings was studied using Tafel Electrochemical Polarization test. The self-healing properties of the materials were also studied by applying cuts on the material and letting them heal under elevated temperatures, and the results showed that the prepared coating demonstrated an effective corrosion resistance for mild steel for various marine application

Bio-Vitrimers for Sustainable Circular Bio-Economy

The aim to achieve sustainable development goals (SDG) and cut CO2-emission is forcing researchers to develop bio-based materials over conventional polymers. Since most of the established bio-based polymeric materials demonstrate prominent sustainability, however, performance, cost, and durability limit their utilization in real-time applications. Additionally, a sustainable circular bioeconomy (CE) ensures SDGs deliver material production, where it ceases the linear approach from production to waste. Simultaneously, sustainable circular bio-economy promoted materials should exhibit the prominent properties to involve and substitute conventional materials. These interceptions can be resolved through state-of-the-art bio-vitrimeric materials that display durability/mechanical properties such as thermosets and processability/malleability such as thermoplastics. This article emphasizes the current need for vitrimers based on bio-derived chemicals; as well as to summarize the developed bio-based vitrimers (including reprocessing, recycling and self-healing properties) and their requirements for a sustainable circular economy in future prospects

Vat Photopolymerization 3D-Printing of Dynamic Thiol-Acrylate Photopolymers Using Bio-Derived Building Blocks

As an energy-efficient additive manufacturing process, vat photopolymerization 3D-printing has become a convenient technology to fabricate functional devices with high resolution and freedom in design. However, due to their permanently crosslinked network structure, photopolymers are not easily reprocessed or repaired. To improve the environmental footprint of 3D-printed objects, herein, we combine the dynamic nature of hydroxyl ester links, undergoing a catalyzed transesterification at elevated temperature, with an acrylate monomer derived from renewable resources. As a sustainable building block, we synthesized an acrylated linseed oil and mixed it with selected thiol crosslinkers. By careful selection of the transesterification catalyst, we obtained dynamic thiol-acrylate resins with a high cure rate and decent storage stability, which enabled the digital light processing (DLP) 3D-printing of objects with a structure size of 550 µm. Owing to their dynamic covalent bonds, the thiol-acrylate networks were able to relax 63% of their initial stress within 22 min at 180 °C and showed enhanced toughness after thermal annealing. We exploited the thermo-activated reflow of the dynamic networks to heal and re-shape the 3D-printed objects. The dynamic thiol-acrylate photopolymers also demonstrated promising healing, shape memory, and re-shaping properties, thus offering great potential for various industrial fields such as soft robotics and electronics

A bibliometric survey of research trends in vitrimer

The recent trends of vitrimer studies enhance the thermoset material with superior properties, therefore, it is particularly important to address the critical scientific inquiries in this area using their research metrics. The reported vitrimer systems have been highly required for future real-time applications; however, the inquisitiveness of material exchange mechanisms extends the research studies further. Significantly, more scientific information's are required to achieve the evident prospective outcomes via these materials. This article highlights the trends and developments of the most relevant publications, authors, articles, countries, and keywords in the vitrimer research field over the past 10 years. The represented bibliometric survey would elevate the basic understanding of the current vitrimer research stats and also help follow the particular research community to learn and develop insight. To generate bibliometric networks, bibliometric data has obtained from Scopus and visualised in VOS-viewer; as an overview of that, the highest number of publications were from China, United States, France, United Kingdom, and Spain

Binder-Free Supercapacitors Based on Thin Films of MWCNT/GO Nanohybrids: Computational and Experimental Analysis

This work reports an innovative approach to the fabrication of free-standing thin films of multiwalled carbon nanotubes (MWCNTs)/graphene oxide (GO) nanohybrids by using dimethyl formamide (DMF) and n-hexane as a solvent–antisolvent system for the growth of thin films of MWCNTs/GO nanohybrids. The synthesis of the GO was carried out by using the modified Hummers method, while the synthesis of MWCNTs/GO nanohybrids was done by the intermixing of the carboxylic acid functionalized MWCNT and GO using the solution-mixing method. The growth of the thin film of MWCNTs/GO nanohybrids was done by obeying the surface-tension-driven phenomena which occur mainly due to the coalescence of bubbles due to the solvent–antisolvent interfacial tension. Furthermore, density functional theory (DFT)-based first-principles simulations were performed to understand the structural, electronic, and capacitive aspects of MWCNT/GO nanohybrids. The computational results demonstrated excellent quantum capacitance in the MWCNT/GO nanohybrid electrodes. Inspired by the computational results, the same process elaborated above has also been employed to develop binder-free supercapacitor devices utilizing the MWCNT/GO nanohybrid as an electrode material. The electrochemical performance of this electrode in 1 M aqueous H2SO4 demonstrates a good energy density of 21.63 WhKg−1 at a current density of 0.5 Ag−1, with a high specific capacitance of 369.01 F/g at the scan rate of 2 mVs−1 and excellent cyclic stability of 97% for 5000 charge–discharge cycles

Binder-Free Supercapacitors Based on Thin Films of MWCNT/GO Nanohybrids: Computational and Experimental Analysis

This work reports an innovative approach to the fabrication of free-standing thin films of multiwalled carbon nanotubes (MWCNTs)/graphene oxide (GO) nanohybrids by using dimethyl formamide (DMF) and n-hexane as a solvent–antisolvent system for the growth of thin films of MWCNTs/GO nanohybrids. The synthesis of the GO was carried out by using the modified Hummers method, while the synthesis of MWCNTs/GO nanohybrids was done by the intermixing of the carboxylic acid functionalized MWCNT and GO using the solution-mixing method. The growth of the thin film of MWCNTs/GO nanohybrids was done by obeying the surface-tension-driven phenomena which occur mainly due to the coalescence of bubbles due to the solvent–antisolvent interfacial tension. Furthermore, density functional theory (DFT)-based first-principles simulations were performed to understand the structural, electronic, and capacitive aspects of MWCNT/GO nanohybrids. The computational results demonstrated excellent quantum capacitance in the MWCNT/GO nanohybrid electrodes. Inspired by the computational results, the same process elaborated above has also been employed to develop binder-free supercapacitor devices utilizing the MWCNT/GO nanohybrid as an electrode material. The electrochemical performance of this electrode in 1 M aqueous H2SO4 demonstrates a good energy density of 21.63 WhKg−1 at a current density of 0.5 Ag−1, with a high specific capacitance of 369.01 F/g at the scan rate of 2 mVs−1 and excellent cyclic stability of 97% for 5000 charge–discharge cycles

Functional structural nanocomposites with integrated self-healing ability

The use of aeronautical thermosetting resins in the field of structural materials is still limited because of several drawbacks, such as the absence of electrical and thermal conductivity and the poor impact damage resistance. An important contribution for increasing the composite application in this field can be given by implementing a strategy of autonomous damage-repair and other specific functions integrated into the material structure. This work proposes a successful strategy based on the design of supramolecular self-healing systems. It is aimed at developing self-healing, load-bearing structures with all functionalities integrated into a single material able to fulfill important industrial requirements

Nitrogen-doped graphene stabilized copper nanoparticles for Huisgen [3+2] cycloaddition "click" chemistry

Nitrogen-doped reduced graphene oxide (NRGO) stabilized copper nanoparticles are designed to assist Cu(I)-catalyzed Huisgen [3+2] cycloaddition "click" chemistry (CuAAC). This study demonstrates a robust route for the synthesis of vastly dispersed heterogeneous catalysts (NRGO/Cu2O), achieving CuAAC at low temperaturewithout any external additive (oxidizing/reducing agent) with high stability and recyclability. Underlying mechanisms are analysed using DFT calculations, confirming the experimental results