Studies on Recycling Silane Controllable Recovered Carbon Fiber from Waste CFRP

During the production process of commercial carbon fiber reinforced polymers (CFRPs), a silane coupling agent is added to the carbon fiber at the sizing step as a binder to enhance the product’s physical properties. While improving strength, the silane coupling agent results in a silane residue on recovered carbon fibers (rCF) after recycling, which is a disadvantage when using recovered carbon fibers in the manufacture of new materials. In this study, the rCF is recovered from waste carbon fiber reinforced polymers (CFRPs) from the bicycle industry by a microwave pyrolysis method, applying a short reaction time and in an air atmosphere. Moreover, the rCF are investigated for their surface morphologies and the elements present on the surface. The silicon element content changes with pyrolysis temperature were 0.4, 0.9, and 0.2%, respectively, at 450, 550, and 650 °C. Additionally, at 950 °C, silicon content can be reduced to 0.1 ± 0.05%. The uniformity of microwave pyrolysis recycle treatment was compared with traditional furnace techniques used for bulk waste treatment by applying the same temperature regime. This work provides evidence that microwave pyrolysis can be used as an alternative method for the production of rCFs for reuse applications.

Synthesis of Substrate-bound Seaweed-like Au Nanowires with Amino Silane Coupling Agents

Seaweed-like Au nanowires were synthesized without any nanoparticle seeds. The amino silcane coupling agent 3-aminopropyltriethoxysilane was used to form the active surface on Au substrate to facilitate one dimensional growth....

Nanoarchitectonics of BN/AgNWs/Epoxy Composites with High Thermal Conductivity and Electrical Insulation

To promote the construction of the thermal network in the epoxy resin (EP), a certain proportion of silver nanowires (AgNWs) coupled with the hexagonal boron nitride (BN) nanoplates were chosen as fillers to improve the thermal conductivity of EP resin. Before preparing the composites, BN was treated by silane coupling agent 3-aminopropyltriethoxysilane (KH550), and AgNWs was coated by dopamine hydrochloride. The BN/AgNWs/EP composites were prepared after curing, and the thermal conductivity and dielectric properties of the composites was tested. Results showed that the AgNWs and BN were uniformly dispersed in epoxy resin. It synergistically built a thermal network and greatly increased the thermal conductivity of the composites, which increased 9% after adding AgNWs. Moreover, the electrical property test showed that the addition of AgNWs had little effect on the dielectric constant and dielectric loss of the composites, indicating a rather good electrical insulation of the composites.

Dye-sensitised Photocatalyst for Photocatalytic Whole Water Splitting to Produce Hydrogen in a Twin Photoreactor

Organic dye-sensitised SrTiO3:Rh and WO3 were served as H2 catalysts and O2 catalysts in a Z-scheme system to conduct photocatalytic pure water splitting. To enhance the light absorption capacity, the composites of organic dye (N3, N719, Z907, black dye, C101, and K19) and SrTiO3:Rh were synthesised via physical adsorption and then verified by the performance of photocatalytic hydrogen evolution. Among these dyes, N3-SrTiO3:Rh revealed visible light absorption and exhibited the best photocatalytic activity. Therefore, N3 dye was adopted, and silane coupling agents were used to form chemical bonding with SrTiO3:Rh. Furthermore, the photocatalytic pure water splitting of N3-SrTiO3:Rh was investigated in a single reactor, and a twin photoreactor with Fe2+ and Fe3+ ions served as the electron mediators, respectively. The highest quantum efficiency can reach 0.0259% in a twin reactor when compared with the single reactor (0.0052%) because of the improvement in the light absorption from N3 and inhibition of the backward reaction of water splitting. Consequently, organic dye-sensitised photocatalysts are highly effective and eco-friendly in conducting photocatalytic pure water splitting.

In Situ Polymerization to Boron Nitride-Fluorinated Poly Methacrylate Composites as Thin but Robust Anti-Corrosion Coatings

High-performance anti-corrosion coatings featuring easy processability and thin thickness are highly desired in industry. Yet, solution process coating often faces a sedimentation problem with particles which are used as reinforcement in coatings. In this contribution, boron nitride (BN) was modified by an acrylate silane coupling agent (KH-570) to obtain acrylated BN flakes. Afterwards, the acrylated BN flakes were in situ copolymerized with 2-(perfluorohexyl)ethyl methacrylate to synthesize BN-fluorinated poly methacrylate (PFBP) composites. The as-obtained PFBP composites can form stable coating solutions, in which sedimentation of BN flakes seldom happens. The coating solution can easily form uniform coatings on various substrates with nanoscale thickness, confirmed by scanning electron microscope (SEM). The corrosion resistance of the samples coated PFBP coatings in 3.5 wt.% sodium chloride solution was evaluated by electrochemical impedance spectroscopy (EIS). It is indicated that the incorporation of BN flakes greatly reduce the corrosion rate. Adhesion measurements and abrasion resistance test indicate the PFBP coating performs good adhesion to substrate and robustness. Through the in situ polymerization, acrylated BN flakes are connected with the polymer chain, which inhibits the sedimentation of BN in the coating solution. Additionally, the BN flakes dispersed in the fluorinated polymer act as barriers, improving the corrosion resistance of the coated samples.