Precise Synthesis of ABCDE Star Quintopolymers by Combination of Controlled Polymerization and Azide–Alkyne Cycloaddition Reaction

A facile approach based on integrated utilization of ring-opening polymerization (ROP), reversible addition–fragmentation chain transfer (RAFT) process, and azide–alkyne cycloaddition reaction was efficiently used to construct amphiphilic 5-arm ABCDE star quintopolymers. The miktoarm stars are composed of poly­(ethylene glycol) (A), poly­(ε-caprolactone) (B), polystyrene (C), poly­(l-lactide) (D), poly­(<i><i>N,N</i></i>-dimethylaminoethyl methacrylate) (E₁), poly­(methyl methacrylate) (E₂), and poly­(methyl acrylate) (E₃). Alkyne-in-chain-functionalized BC and DE diblock copolymers were synthesized by successive ROP and RAFT process. Selective [3 + 2] click reaction between two-azide-end-functionalized PEG and BC copolymer gave azide-core-functionalized ABC star terpolymer, and a subsequent click reaction with DE copolymer afforded well-defined ABCDE stars with well-controlled molecular weight, low polydispersity, and precise composition, as evidenced from ¹H NMR, GPC, and GPC-MALLS analyses. DSC analyses revealed part of polymer segments in ABCDE stars were compatible. This general methodology has some advantages such as straightforward synthesis, mild reaction conditions, versatile polymerizable monomers, and high yields, which is promising for the construction of numerous functional star copolymers with multiple compositions and precise microstructures

In Situ Growth of Core–Sheath Heterostructural SiC Nanowire Arrays on Carbon Fibers and Enhanced Electromagnetic Wave Absorption Performance

Large-scale core–sheath heterostructural SiC nanowires were facilely grown on the surface of carbon fibers using a one-step chemical vapor infiltration process. The as-synthesized SiC nanowires consist of single crystalline SiC cores with a diameter of ∼30 nm and polycrystalline SiC sheaths with an average thickness of ∼60 nm. The formation mechanisms of core–sheath heterostructural SiC nanowires (SiC_nws) were discussed in detail. The SiC_nws-CF shows strong electromagnetic (EM) wave absorption performance with a maximum reflection loss value of −45.98 dB at 4.4 GHz. Moreover, being coated with conductive polymer polypyrrole (PPy) by a simple chemical polymerization method, the SiC_nws-CF/PPy nanocomposites exhibited superior EM absorption abilities with maximum RL value of −50.19 dB at 14.2 GHz and the effective bandwidth of 6.2 GHz. The SiC_nws-CF/PPy nanocomposites in this study are very promising as absorber materials with strong electromagnetic wave absorption performance

Ordered Silica Nanoparticles Grown on a Three-Dimensional Carbon Fiber Architecture Substrate with Siliconborocarbonitride Ceramic as a Thermal Barrier Coating

Hierarchical structure consisting of ordered silica nanoparticles grown onto carbon fiber (CF) has been fabricated to improve the interfacial properties between the CFs and polymer matrix. To improve the reactivity of CFs, their surface was modified using poly­(1,4-phenylene diisocyanate) (PPDI) via in situ polymerization, which also resulted in the distribution of numerous isocyanate groups on the surface of CFs. Silica nanoparticles were modified on the interface of CF-PPDI by chemical grafting method. The microstructure, chemical composition, and interfacial properties of CFs with ordered silica nanoparticles were comprehensively investigated by scanning electron microscopy, X-ray photoelectron spectroscopy, and Fourier transform infrared spectroscopy. Results indicated an obvious increase in the interfacial shear strength, compared to that of CF precursor, which was attributed to silica nanoparticles interacting with the epoxy resin. Furthermore, siliconborocarbonitride (SiBCN) ceramic was used as thermal barrier coating to enhance 3D CF architecture substrate antioxidant and ablation properties. Thermogravimetric results show that the thermal stability of the CF with SiBCN ceramic layer has a marked increase at high temperature