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Surface initiated electro-polymerization of acrylamide on carbon fiber with methodically varied amounts of acrylamide monomer and N,N′-methylene bis-acrylamide crosslinker is explored in this study. The effect of the polymer coating on tensile strength, Young's modulus, and interfacial properties of carbon fibre in an epoxy resin was determined. A significant improvement in tensile strength, tensile modulus, and interfacial shear strength (IFSS) across all modified samples was observed, with the most notable improvements to tensile strength, tensile modulus and IFSS being 38%, 15% and 192.5%, respectively. This covalently bound polymer coating provides the best kind of solution for the two most crucial limitations of carbon fibre, with the minimum amount of effort, time, and cost.

We report the preparation of thermoresponsive block copolymers via the simultaneous RAFT polymerization and anionic ring-opening polymerization (ROP) of N-isopropylacylamide and ε-caprolactone respectively, in the absence of traditional solvents.

Bonding dissimilar materials has been a persistent challenge for decades. This paper presents a method to modify a stainless steel surface (316 L), routinely used in medical applications to enable the significant adhesion of a biopolymer (silk fibroin). The metallic surface was first covalently grafting with polyacrylamide, to enable a hydrogen bonding compatible surface. The polymerisation was initiated via the irreversible electrochemical reduction of a 4-nitrobenzene diazonium salt (20 mM), in the presence of an acrylamide monomer (1 M) at progressively faster scan rates (0.01 V/s to 1 V/s). Examination of the modified samples by FT-IR was consistent with successful surface modification, via observations of the acrylamide carbonyl (1600-1650 cm

An insulating composite was made from the sustainable building blocks wool, sulfur, and canola oil. In the first stage of the synthesis, inverse vulcanization was used to make a polysulfide polymer from the canola oil triglyceride and sulfur. This polymerization benefits from complete atom economy. In the second stage, the powdered polymer is mixed with wool, coating the fibers through electrostatic attraction. The polymer and wool mixture is then compressed with mild heating to provoke S-S metathesis in the polymer, which locks the wool in the polymer matrix. The wool fibers impart tensile strength, insulating properties, and flame resistance to the composite. All building blocks are sustainable or derived from waste and the composite is a promising lead on next-generation insulation for energy conservation.

A key factor determining the performance of carbon fibre reinforced polymer (CFRP) composites is their fibre-to-matrix interactions, the interface and interphase, as these allow for the efficient transfer of stress from the relatively weak and ductile resin to the strong reinforcing fibres. The manipulation of the interface via modulation of surface chemistry has been been an active area of research with many apporaches being taken. In this work we cover efforts in this area from traditional manufacturing condition optimisations, plasma, wet chemical, and electrochemical approaches to induce favourable properties in composites. The design of molecular interactions at the interface are exceedingly difficult to determine and design, and thus, we finish this review with a section on the use of molecular dynamics to design complementary interfaces for the next generation of composites.

The ability to rapidly modify the surface of materials is a powerful means of tailoring interfaces and interphases for a variety of applications. In this work, we demonstrate the extensive scope of an electrochemically mediated surface modification technique, able to install a range of surface grafted polymers of varying polarity and functionality. The irreversible reduction of aryldiazonium salts initiates polymer growth and provides a "priming layer" for the polymers to attach to, covalently anchoring them to the surface. We show the broad applicability of this technique through polymerization of 19 acrylate monomers, as well as a noncarbonyl bearing monomer species, styrene. Surface bound films were characterized using FT-IR, ellipsometry, and water contact angle.

Silk fibroin is an excellent biopolymer for application in a variety of areas, such as textiles, medicine, composites and as a novel material for additive manufacturing. In this work, silk membranes were surface modified by in situ polymerization of aqueous acrylic acid, initiated by the reduction of various aryldiazonium salts with vitamin C. Treatment times of 20 min gave membranes which possessed increased tensile strength, tensile modulus, and showed significant increased resistance to needle puncture (+131%), relative to &lsquo, untreated&rsquo, standards. Most interestingly, the treated silk membranes were able to be reversibly formed into various shapes via the hydration and plasticizing of the surface bound poly(acrylic acid), by simply steaming the modified membranes. These membranes and their unique properties have potential applications in advanced textiles, and as medical materials.

Silk fibroin is an excellent biopolymer for application in a variety of areas, such as textiles, medicine, composites and as a novel material for additive manufacturing. In this work, silk membranes were surface modified by in situ polymerization of aqueous acrylic acid, initiated by the reduction of various aryldiazonium salts with vitamin C. Treatment times of 20 min gave membranes which possessed increased tensile strength, tensile modulus, and showed significant increased resistance to needle puncture (+131%), relative to ‘untreated’ standards. Most interestingly, the treated silk membranes were able to be reversibly formed into various shapes via the hydration and plasticizing of the surface bound poly(acrylic acid), by simply steaming the modified membranes. These membranes and their unique properties have potential applications in advanced textiles, and as medical materials.

This work demonstrates the introduction of a phosphonate moiety into a commonly used curing agent, 4,4′-diaminodiphenylmethane (DDM), via an α-aminophosphonate. This compound (DDMP) can be prepared and isolated in analytical purity in under 1 h and in good yield (71 %). Thermoset polymer (epoxy-derived) samples were prepared using a room-temperature standard cure (SC) and a post-cured (PC) protocol to encourage incorporation of the α-aminophosphonate into the polymer network, with improved flammability properties observed for the latter. Thermogravimetric analysis under a nitrogen atmosphere showed increased char yield at 600°C, and similar observations were made when analysis was conducted in air. Significant reductions in flammability are observed at very low phosphorus content (P% = 0.16–0.49 %), demonstrated by higher char yields (25.5 from 14.0 % in air), decreased burn time from ignition (60 to 24 s), and decreased mass loss after ignition (87.6 to 58.5 %). Limiting Oxygen Index for the neat polymer (P% = 0 %, 20.3 ± 0.8 %) increased with increasing α-aminophosphonate additive (P% = 0.16 %, 20.8 ± 0.6 %; P% = 0.32 %, 21.4 ± 0.4 %; P% = 0.49 %, 22.6 ± 0.8 %).

International audience; Colored and color-changing materials are central to perception and interaction in nature and have been exploited in an array of modern technologies such as sensors, visual displays and smart materials. Attempts to introduce color into carbon fiber materials have been limited by deleterious impacts on fiber properties, and the extension of colored fibers towards 'smart composites' remains in its infancy. We present carbon fibers incorporating structural color, similar to that observed on the surface of soap bubbles and various insects and birds, by modifying the fiber surface through in situ polymerization grafting. When dry, the treated fibers exhibit a striking blue color, but when exposed to a volatile solvent, a cascade of colors across the visible region is observed as the film first swells and then shrinks as the solvent evaporates. The treated fibers not only possess a unique color and color-changing ability, but can also be reversibly formed into complex shapes and bear significant loads even without being encased in a supporting polymer. The tensile strength of treated fibers shows a statistically significant increase (+12%) and evaluation of the fiber-to-matrix adhesion of these polymers to an epoxy resin shows more than 300% improvement over control fibers. This approach creates a new platform for the multifaceted advance of smart composites.

Testing methodologies to accurately quantify interfacial shear strength (IFSS) are essential in order to understand fiber-matrix adhesion. While testing methods at a microscale (single filament fragmentation test—SFFT) and macroscale (Short Beam Shear—SBS) are wide spread, each have their own shortcomings. The Iosipescu (V-notch) tow test offers a mesoscale bridge between the microscale and macroscale whilst providing simple, accurate results with minimal time investment. However, the lack of investigations exploring testing variables has limited the application of Iosipescu testing to only a handful of studies. This paper assesses the effect of carbon fiber tow size within the Iosipescu tow test for epoxy resin. Tow sizes of 3, 6, and 9 k are eminently suitable, while more caution must be shown when examining 12, and 15 k tows. In this work, tows at 18 and 24 k demonstrated failure modes not derived from interfacial failure, but poor fiber wetting. A catalogue of common fracture geometries is discussed as a function of performance for the benefit of future researchers. Finally, a comparison of commercial (T300), amine (T300-Amine), and ethyl ester (T300-Ester) surface modified carbon fibers was conducted. The outcomes of this study showed that the Iosipescu tow test is inherently less sensitive in distinguishing between similar IFSS but provides a more ‘real world’ image of the carbon fiber-epoxy interface in a composite material.