Abstract Environmental friendliness and cost demand the development of lignin-modified phenolic (LPF) resins for application as a binder for carbon-containing refractories (CCRs) production. Moreover, the in-situ graphitization of such resins can produce crystalline carbon, which is an essential component of CCRs. Consequently, this study investigated LPF resins graphitization using ferrocene, boron oxide and boric acid. The modified resins were synthesized using thermally treated kraft lignin based on 1.5 formaldehyde to phenol molar ratio and with up to 30 wt.% lignin as phenol replacement. The resins chemical composition and the structural organization and oxidation resistance of carbons derived from the plain resins and those containing the graphitizing additives were determined. The results showed that ferrocene and the boron compounds could induce graphitic carbon generation when carbonizing LPF resins at 1500 °C for 5 hours. The best graphitization level (73%) was achieved when 10 wt.% boric acid was added to the resin produced with 20 wt.% lignin. Regarding the formulations containing ferrocene, the highest amount of graphitic carbon (48%) was generated when 5 wt.% of this additive was added to the resin synthesized with 10 wt.% lignin. The carbons derived from the formulations containing boron oxide presented the best oxidation resistance.

The effect of maleic anhydride (MA) content on morphological, thermal, thermomechanical and mechanical properties of PA6/AES/MMA-MA (66.5/28.5/5 wt%) system was investigated. In general, the simple incorporation of MMA-MA to PA6/AES system is responsible for enhancements in mechanical performance. PA6/AES/MMA-MA3% and PA6/AES/MMA5% exhibited similar morphology and final properties, indicating no MA content effect on the studied system. On the other hand, PA6/AES/MMA-MA10% exhibited a quite different morphology and lower mechanical performance compared to the other compatibilized blends. Such unexpected behavior was not attributed to the effective maleic anhydride content in this composition, but to the reduced molar mass resulted from the excess of non-reacted MA monomer during the synthesis procedure.

This review reports the preparation and characterization of bionanocomposites based on biodegradable polymers reinforced with cellulose nanocrystals (CNC) described in the literature. The outstanding potential of cellulose nanocrystals as reinforcement fillers of biodegradable polymers is presented with an emphasis on the solution casting process, which is an appropriate method to investigate the physico-chemical effects of the incorporation of CNC into the polymeric matrices. Besides solution casting, other small scale methods such as electrospinning and layer-by-layer are also covered.