In the present work, foamed polypropylene (PP) composites were prepared by chemical foaming technology, and the foaming quality and impact property of the foamed PP composites were studied. The results showed that the foaming quality was significantly improved after the introduction of thermoplastic rubber (TPR) and polyolefin elastomer (POE). Meanwhile, it was found that the impact property depended on the intrinsic toughness and contribution of foams (cells) to the PP composites. Furthermore, the data regarding impact property in low temperature showed that when the temperature was between −80 and −20 °C, the impact properties of the foamed PP composites were higher than that of the unfoamed sample, which was due to the impact property being completely contributed by cells under this condition. Meanwhile, when the temperature ranged from −20 to 20 °C, the impact property of the unfoamed sample was higher, which was due to the PP matrix contributing more to the impact property under this temperature. This work significantly improved the foaming quality of foamed PP composites and provided reliable evidence for the improvement of impact property.

The effects of the cell size and distribution on the mechanical properties of polypropylene foam were simulated and analyzed by finite element modeling with ANSYS and supporting experiments. The results show that the reduced cell size and narrow size distribution have beneficial influences on both the tensile and impact strengths. Decreasing the cell size or narrowing the cell size distribution was more effective for increasing the impact strength than the tensile strength in the same case. The relationship between the mechanical properties and cell structure parameters has a good correlation with the theoretical model.

Polyamide 6 (PA6) was modified with ethylene maleic anhydride syndiotactic copolymer resin (ZeMac), and triglycidyl isocyanurate (TGIC) as modifiers to prepare a grafting structure and a long-chain branching structure, respectively. The effects of two modifiers on the rheological behavior, crystallization properties, foaming performance, and mechanical properties of PA6 were systematically studied by rotating rheometry, differential scanning calorimetry and scanning electron microscopy. The results showed that there were differences in crystallization properties between the two modification methods, but they significantly improved the rheological, foaming performance, and mechanical properties of PA6. In particular, PA6 with long-chain branching structure through TGIC modification showed better performance in various physicochemical characterizations. The introduction of ZeMac reduced the average diameter of bubbles in pure PA6 from 146.32 to 88.12 µm, and the density of bubbles increased from 1.69 × 10 ⁵ to 5.35 × 10 ⁵ cells·cm ⁻³ . The introduction of TGIC reduced the average diameter of bubbles in pure PA6 from 146.32 to 64.36 µm, and the density of bubbles increased to 1.31 × 10 ⁶ cells·cm ⁻³ . Moreover, the mechanical properties of both nonfoamed and foamed samples were improved after modification.

Three types of organic cage compounds, namely, cucurbit[6]uril (Q[6]), hemicucurbit[6]uril (HQ[6]), and β-cyclodextrin (BC), with different cavity structures as heterogeneous nucleation agents were selected for a polypropylene (PP) foaming injection molding process. The experimental results showed that Q[6] with a “natural” cavity structure possessed the best nucleation efficiency of these three cage compounds. The nucleation mechanism of organic cage compounds was explored through classical nucleation theory, molecular structure, and in situ visual injection molding analysis.