Xiaochao Liu

A new bio-based polyamide 56/512 (PA56/512) has been synthesized with a higher bio-based composition compared to industrialized bio-based PA56, which is considered a lower carbon emission bio-based nylon. In this paper, the one-step approach of copolymerizing PA56 units with PA512 units using melt polymerization has been investigated. The structure of the copolymer PA56/512 was characterized using Fourier-transform infrared spectroscopy (FTIR) and Proton nuclear magnetic resonance (¹H NMR). Other measurement methods, including relative viscosity tests, amine end group measurement, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC), were used to analyze the physical and thermal properties of the PA56/512. Furthermore, the non-isothermal crystallization behaviors of PA56/512 have been investigated with the analytical model of Mo’s method and the Kissinger method. The melting point of copolymer PA56/512 exhibited a eutectic point at 60 mol% of 512 corresponding to the typical isodimorphism behavior, and the crystallization ability of PA56/512 also displayed a similar tendency.

The purpose of this study was to investigate the structural evolution and properties of simultaneously biaxially stretched polyamide‐6/poly(ether block amide) copolymer (PA6/PEBA) films. The results showed the melting temperature of PA6 increased from 220.02°C to 225.56°C when the stretching ratios increased from 1 × 1 to 3.5 × 3.5, suggesting the occurrence of β → α crystal transformation. Meanwhile, the increase of stretching ratios increased the crystallinity of the films due to the molecular orientation, which could create a more tortuous path for the diffusion of oxygen molecules through the films. As a result, the oxygen barrier performance of the stretched PA6/PEBA film was increased after biaxial stretching. The morphological observation showed that spherical or slightly ellipsoidal PEBA particles were dispersed in the PA6 matrix. The thermal shrinkage of the stretched film increased as the stretching ratios increased, and no significant difference of the shrinkage between machine direction (MD) and transition direction (TD) was observed in the stretched films. It was also found that the tensile strength of the stretched films in MD and TD exhibited the highest value at a stretching ratio of 3.5 × 3.5, which was about 1.7 times and 2.1 times higher than that of the unstretched PA6/PEBA film, respectively.

Biaxially oriented polyamide‐6 (BOPA) film has been widely used in many packaging applications. However, the BOPA film with excellent toughness is still required when utilizing in the field of soft‐packaged lithium‐ion batteries, pharmaceutical blister packaging, or frozen food packaging especially for vacuum packaging of irregular‐shaped food products. The purpose of this study was to improve the toughness of BOPA films by toughening with poly(ether block amide) (PEBA) (BOPA/PEBA films) based on the simultaneous biaxial stretching technology. The crystal structure, morphology, optical properties, barrier, and mechanical properties of BOPA/PEBA films were investigated. The results showed that the incorporation of PEBA into BOPA films slightly decreased the melting temperature and crystallinity of PA6, and the BOPA/PEBA films exhibited only α‐form crystals and no preferential orientation in the machine direction (MD) and transition direction (TD). The morphological observation showed that higher addition of PEBA led to the formation of microvoids due to the poor compatibility between PA6 and PEBA. As a result, the transmittance and oxygen barrier properties of the BOPA/PEBA films decreased. In addition, mechanical analysis suggested that the addition of PEBA could effectively improve the toughness of BOPA film.

Stretching has a significant effect on the microstructure and ultimate performance of semi-crystalline polymers. To investigate the effect of stretching on structure and mechanical properties of uniaxial stretched PA612/SiO₂, PA612 and PA612/SiO2 films were prepared at four temperatures close to the glass transition temperature at various strain. The samples were characterized by a transmission electron microscope (TEM), wide-angle X-ray diffractometer (WAXD), Two-dimensional wide-angle X-ray Scattering (2D-WAXS), differential scanning calorimeter (DSC), dynamic mechanical analyzer (DMA), and stretching tests. The results showed that the α phase was the dominant phase in PA612 casting film, no obvious γ phase was observed, while both stretching and the presence of SiO₂ can induce the generation of α phase and improve the crystallinity of PA612. Crystals were oriented along the stretching direction and the b axis was parallel to the equatorial direction after stretching. The interplanar spacing of (010/110) decreased with the increasing stretching temperature and expanded with the increasing strain, while stretching temperature and strain present negligible effect on the interplanar spacing of (100). The grain size increased with the stretching temperature while decreased with strain. The presence of SiO₂ led to reduce the yield stress and the stress drop beyond yielding of the composite. Uniaxial stretching gave rise to a significant improvement in the fracture stress and the glass transition temperature.

Polyamide 6–66 (PA6‐66)–montmorillonite (MMT)–nanosilica (NS) nanocomposite films were fabricated through a cast film process and then biaxially stretched on a laboratory stretcher. Uniaxial or biaxial stretching induced the elongated conformation of MMT and NS. The b axis of the α crystals and the amorphous phase were revealed to align along the machine direction (MD) after stretching, with the uniaxial orientation playing a more significant role. Furthermore, the crystallinity of PA6‐66 stretching increased with the stretching ratio. Uniaxial stretching gave rise to a significantly enhanced tensile strength along the MD, whereas it slightly decreased the mechanical properties along the transverse direction (TD). In contrast, the films subjected to biaxial stretching exhibited more balanced mechanical properties. Uniaxial and biaxial stretching led to decreased transmittance and increased haze in the PA6‐66–MMT–NS films; this could have been due to the elongated nanostructure of the two nanofillers, which inhibited the transmission and facilitated the scattering of visible light. The thermal shrinkage of the films increased with increasing stretching ratio, and the biaxially oriented films presented nearly equal shrinkage in the MD and TD. The addition of nanofillers decreased the shrinkage attributed to the mobility inhibition of the polymer chains during heating. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 136, 47504.