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We reveal an unexpected spontaneously dynamic oxygen migration on carbon nanotubes, which is attributed to low reaction barriers for the C-O bond breaking/reforming reactions or the proton transfer between the neighboring epoxy and hydroxyl groups.

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Poly(methyl acrylate)-b-poly(N-vinyl pyrrolidone/maleic anhydride/styrene) (PMA-b-P (NVP/MAH/St)) quaternary amphiphilic block copolymer prepared by reversible addition-fragmentation chain transfer (RAFT) was used to improve the anti-hydrolysis and dispersion properties of aluminum nitride (AIN) powders that were modified by copolymers. Its structure was characterized by Fourier transform infrared spectroscopy (FT-IR) and Hydrogen nuclear magnetic spectroscopy (1H-NMR). The results demonstrate that the molecular weight distribution of the quaternary amphiphilic block copolymers is 1.35–1.60, which is characteristic of controlled molecular weight and narrow molecular weight distribution. Through charge transfer complexes, NVP/MAH/St produces a regular alternating arrangement structure. After being treated with micro-crosslinking, AlN powder modified by copolymer PMA-b-P(NVP/MAH/St) exhibits outstanding resistance to hydrolysis and can be stabilized in hot water at 50 °C for more than 14 h, and the agglomeration of powder particles was improved remarkably.

Developing new coating modification technology of aluminum nitride (AlN) powder for higher hydrolysis resistance is the key to prepare high-performance AlN ceramic substrate with water-based wet process in the future. In the this paper, The poly(vinyl pyrrolidone)-b-poly(Styrene/Itaconic anhydride) (PVP-b-P(St/ITA))block copolymer with PVP as the independent chain segment was designed and synthesized through reversible addition fragmentation chain transfer (RAFT) polymerization, which was used for the study on coating modification, hydrolysis resistance, and dispersion performance of AIN powder. The study results show that, when using PVP macromolecular chain transfer agent (PVP-CTA) for the RAFT chain extension and polymerization in St/ITA binary system, the molecular weight increases linearly and the molecular weight distribution tends to decrease with the monomer conversion rate, which is in line with the activity-controlled characteristics of RAFT polymerization. The copolymer PVP-b-P(St/ITA) was used to for surface modification treatment of submicron AlN powder to generate esterification reaction, which was absorbed and bound to the powder surface. Hydrolysis resistance and dispersion experiments were conducted for modified powder, and the crystal phase and micro structure of modified powder were analyzed and observed through XRD, SEM, and TEM. It was found that copolymer modification had no effect on the powder crystal phase. A 8–21 nm passivation layer was coated on the surface, which can exist stably for 10 h in 60 °C water. Zeta potential and laser particle analyzer tests showed that modified powder featured excellent water-based slurry dispersion performance, and certain self-dispersing characteristics. The highest Zeta potential appeared in pH 6~7, and the particle granularity was distributed uniformly with the median particle diameter of 875 nm. The powder hydrolysis resistance and dispersion performance are significantly improved.