Enhancing cellular structure, mechanical properties, thermal stability and flame retardation of EVA/NR blend nanocomposite foams by silicon dioxide-based flame retardant

Flame retardant rubber foams of ethylene vinyl acetate (EVA)/natural rubber (NR)/layered silicate blends filled with silicon dioxide (SiO2) were prepared by using azodicarbonamide (ADC) as a blowing agent. Specifically, SiO2 was added in EVA/NR blend nanocomposites to produce good flame retardant foams. The properties of EVA/NR blend nanocomposite foams with different SiO2 loading (0, 20, 30, 40 parts per hundred rubber, phr) were investigated through transmission electron microscopy (TEM), scanning electron microscopy (SEM), rheological property test, mechanical property measurement, flammability tests, thermogravimetry analysis (TGA) and pyrolysis-gas chromatography-mass spectrometry (Pyrolysis-GC-MS). Compared with the simple EVA/NR blend nanocomposite, the added SiO2 increased the blend compatibility between EVA and NR phases and melt strength/viscosity of the EVA/NR blend nanocomposites, thus promoting cellular structure of the EVA/NR nanocomposite foams. Increasing SiO2 loading resulted in higher cell density, smaller cell size, and lower volume of void. These improvements caused higher strength and elastomeric recovery. The LOI test results showed that flame retardancy of the EVA/NR blend nanocomposite foams increased at higher SiO2 loading as a result of formation of insulation silicon dioxide-based char. TGA and pyrolysis-GC-MS analyses also validated the finding that the silicon dioxide-based char in the foamed samples containing higher SiO2 loading was more effective on improving thermal stability, which was responsible for lower material combustibility and better flame retardancy. Based on our finding, it was concluded that a good flame retardant EVA/NR blend nanocomposite foam with the best improvement in strength and elastomeric recovery was achieved when combined with 40 phr SiO2.

Physical Hybrid of Nanographene/Carbon Nanotubes as Reinforcing Agents of NR-Based Rubber Foam

Natural rubber (NR) foams reinforced by a physical hybrid of nanographene/carbon nanotubes were fabricated using a two-roll mill and compression molding process. The effects of nanographene (GNS) and carbon nanotubes (CNT) were investigated on the curing behavior, foam morphology, and mechanical and thermal properties of the NR nanocomposite foams. Microscope investigations showed that the GNS/CNT hybrid fillers acted as nucleation agents and increased the cell density and decreased the cell size and wall thickness. Simultaneously, the cell size distribution became narrower, containing more uniform multiple closed-cell pores. The rheometric results showed that the GNS/CNT hybrids accelerated the curing process and decreased the scorch time from 6.81 to 5.08 min and the curing time from 14.3 to 11.12 min. Other results showed that the GNS/CNT hybrid improved the foam’s curing behavior. The degradation temperature of the nanocomposites at 5 wt.% and 50 wt.% weight loss increased from 407 °C to 414 °C and from 339 °C to 346 °C, respectively, and the residual ash increased from 5.7 wt.% to 12.23 wt.% with increasing hybrid nanofiller content. As the amount of the GNS/CNT hybrids increased in the rubber matrix, the modulus also increased, and the Tg increased slightly from −45.77 °C to −38.69 °C. The mechanical properties of the NR nanocomposite foams, including the hardness, resilience, and compression, were also improved by incorporating GNS/CNT hybrid fillers. Overall, the incorporation of the nano hybrid fillers elevated the desirable properties of the rubber foam.

Open porous morphology evolution in poly (butylene succinate)/chitin nanocrystal nanocomposite foams

In recent decades, biodegradable polymeric open-porous foams have been engaging increasing interests owing to their biodegradability, porosity and biocompatibility. In this work, biodegradable poly (butylene succinate) (PBS)/chitin nanocrystals (ChNCs) nanocomposite foams with open porous structure were successful fabricated by a solid-state batch foaming method. ChNCs were obtained from chitin by using sulfuric acid treatment and then introduced into PBS. The incorporation of ChNCs had a positive effect on the crystallization behaviors, melt viscoelasticity and thermal stability of diverse PBS specimens. Compared with the change of foaming temperature, the addition of ChNCs would cause a prominent influence on the open porous structure of diverse PBS foams. The probable explanation was that during the foaming process, the spherulites and/or ChNCs as the hard region in PBS could be served as pore wall and the amorphous area as the soft region was acted as pore, leading to open porous PBS foams. The reported strategy in this work could provide the guidelines to regulate and control open porous foams in other semi-crystalline polymer matrices.

Optimization of Actuation Load and Shape Recovery Speed of Polyester-Based/Fe3O4 Composite Foams

In this research, polyester-based polymers/Fe3O4 nanocomposite foams were prepared in order to study their performance; namely shape recovery speed and actuation load. A foamed structure was obtained through a solid-state foaming process, which was studied and optimized in previous research. The optimum foaming parameters were applied in an attempt to achieve the highest foaming ratio possible. A Taguchi Map was then designed to determine the number of experiments to be conducted. The experimental results showed that the maximum actuation load obtained was 3.35 N, while optimal (fastest) recovery speed was 6.36 mm/min. Furthermore, temperature had no impact on the actuation load as long as a temperature above the Tg was applied. Moreover, the addition of nanoparticles reduced shape recovery speed due to discontinuity within the polymer matrix.