MXene/sPS nanocomposites: rheological, electrical conductivity, polymorphism, mechanical, thermal, and flammability properties.

MXenes as an emerging class of 2D materials have great potential in fabricating functional polymer nanocomposites. In this study, Ti3C2T x MXene as a representative MXene filler was employed to prepare sPS nanocomposites. The abundant surface groups (mainly -OH) on MXene allowed facile modification, and thus MXene nanosheets bearing -C12H25 groups were prepared using dodecyl triethoxysiloxane (DCTES) as a modifier. Grafting -C12H25 long alkyl chains onto the surface of MXene strongly affected its affinity towards hydrophobic solvent and the sPS matrix. The rheological threshold concentration (ϕ c,G' = 0.033 vol%) and exponent (ß G' = 1.51) and the conductivity threshold concentration (ϕ c,σ = 0.259 vol%) and exponent (ß σ = 2.92) were determined by applying percolation scaling laws. The influences of DCTES-modified MXene on the polymorphism, mechanical, thermal and flammability properties of nanocomposites were studied. The obtained nanocomposites displayed not only enhanced mechanical properties, but also improved thermal stability and flame retardancy to some extent. Moreover, the higher the loading level of DCTES-modified MXene, the better was the improved effect.

Synthesis of ultrahigh-molecular-weight ethylene/1-octene copolymers with salalen titanium(iv) complexes activated by methyaluminoxane.

Two salalen titanium(iv) complexes ((H-salalen)TiCl2 and (F-salalen)TiCl2) containing hydrogen and fluorine respectively on the phenolate ring close to the imine were synthesized for the copolymerization of ethylene with 1-octene to prepare poly(ethylene-co-1-octene) in the presence of methylaluminoxane (MAO). The (F-salalen)TiCl2/MAO showed higher catalytic activity and better copolymer characteristics such as a higher molecular weight, narrower molecular weight distribution, and higher 1-octene incorporation than (H-salalen)TiCl2/MAO, which revealed that the electron-withdrawing conjugated effect introduced by fluorine substituents led to improvements on catalytic performance and thermal stability. The influences of copolymerization conditions including temperature, Al/Ti molar ratios and comonomer feed ratios on the copolymerization behavior of (F-salalen)TiCl2/MAO and the copolymer microstructure were investigated in detail. Under the activation of MAO, the (F-salalen)TiCl2 could produce ultrahigh molecular weight poly(ethylene-co-1-octene) with 1-octene incorporation ratios in the range of 0.9-3.1 mol% and exhibit relatively high activity. It could be inferred that long ethylene sequences in the copolymer were segregated by the isolated 1-octene units based on the 13C NMR characterization of the copolymer. Moreover, the thermal properties and crystallization of copolymers were determined by DSC and XRD and correlated to the ethylene sequence length distribution. The reactivity ratios calculated by the triad distribution in 13C NMR revealed the random comonomer distribution in the copolymer chain.