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An urgent need is to reduce the flammability of polymers and manage their toxic thermal decomposition products. Although conventional halogenated, metallic and phosphorus-based flame retardants (FRs) proved effective, they are known to cause major damage to human health and the environment. Containing carbon nanomaterials as a new class of flame retarding additives, polymer nanocomposites have displayed high flame retardancy, mechanical performance and electrical and thermal conductivity – a feat unmatched by conventional FRs. In this article we review very recent advances in carbon nanomaterials as FRs for polymers and composites as well as new understanding of the underpinning flame retarding mechanisms. Carbon nanomaterials, i.e. graphene, carbon nanotubes and carbon black, are discussed as the alternatives to conventional fillers due to their effectiveness in improving the polymers' flammability, mechanical properties and conductivity. The synergy between carbon-based nanofillers and conventional FRs is comprehensively reviewed, concluding that adding small fractions of carbon nanomaterials with conventional FRs into polymers can not only synergistically improve the flame retardancy but result in multifunctionalities such as thermal and electrical conductivity, without compromising the polymers' mechanical performance. Chemically or physically combining carbon nanomaterials with other compounds or nanoadditives containing phosphorus and nitorgen elements can create significant synergies for multifunctional polymers and composites to attain superior flame-retardant properties. [ABSTRACT FROM AUTHOR]

The SiO 2 @metal organic framework (Universitetet i Oslo-66, UiO-66) core–shell microspheres were constructed through covalent linkage between amine groups in UiO-66-NH 2 and epoxy groups on the surface of silica. The morphology and size of the SiO 2 @UiO-66 core–shell microspheres could be simply controlled by tuning the ratio between UiO-66-NH 2 and epoxy terminated silica (E-SiO 2). As observed by TEM, the SiO 2 @UiO-66 hybrids showed better dispersion state within epoxy matrix compared to either E-SiO 2 or UiO-66-NH 2. The incorporation of SiO 2 @UiO-66 hybrids slightly promoted the thermal degradation of the resultant epoxy composites but improved residual yield. The dynamic mechanical analysis results indicated that the SiO 2 @UiO-66 hybrids slightly increased the glass transition temperature and the modulus. The SiO 2 @UiO-66 hybrids exhibited higher efficiency in reducing the heat release rate and the smoke production rate compared to either E-SiO 2 or UiO-66-NH 2. The influence of the component ratio in SiO 2 @UiO-66 on flame retardancy of the epoxy composites was also studied by cone calorimeter. Specifically, the SiO 2 @UiO-66 hybrid with medium ratio (SiO 2 @UiO-66-2) exhibited maximum reduction in peak heat release rate (−31%), total heat release (−23%) and total smoke production (−16%). The char residues were investigated by the Fourier transform infrared spectra, scanning electron microscopy and X-ray photoelectron spectroscopy, which demonstrated that the enhanced flame retardancy of EP/SiO 2 @UiO-66-2 was attributable to the continual morphology and high thermal resistance originated from the presence of the silicon and zirconium complex. These favorable characteristics including high flame retardant efficiency and good smoke suppression make SiO 2 @UiO-66 hybrids promising for flame retardant polymers application. • The SiO 2 @UiO-66 hybrids showed core–shell microsphere structure. • The addition of 3 wt% SiO 2 @UiO-66-2 caused 31% reduction in peak heat release rate. • The addition of 3 wt% SiO 2 @UiO-66-2 led to 16% reduction in total smoke production. [ABSTRACT FROM AUTHOR]