Investigation on the Correlation between Biaxial Stretching Process and Macroscopic Properties of BOPA6 Film

• Published in: Polymers Vol. 16; no. 7; p. 961
• Main Authors: Li, Bowen, Liao, Guangkai, Li, Yuankang, Yin, Haomin, Cui, Lingna, Cao, Kaikai, Xie, Zhenyan, Liu, Jiaxin, Liu, Yuejun
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.04.2024
• Subjects: Analysis; biaxial stretching; Casting; Crystal structure; Crystallinity; Crystallization; Diffusion rate; Hydrogen bonds; Investigations; Mechanical properties; Molecular chains; Nylon; Optical properties; Oxidation; Oxygen; Phase transitions; polyamide 6; Polyamide resins; Polyethylene; Polymers; Pressure casting; Ratios; Raw materials; Rheological properties; rheology; Storage modulus; Stretching rate; Temperature; Tensile strength; China; rheology; barrier properties; crystallization; optical performance; film; biaxial stretching; mechanical properties; polyamide 6
• DOI: 10.3390/polym16070961
• ISSN: 2073-4360

Biaxially oriented polyamide 6 (BOPA6) films were prepared by extrusion casting and biaxial stretching with polyamide 6. The effects of different biaxially oriented on the macroscopic properties of BOPA6 were investigated by characterizing the rheological, crystallization, optical, barrier and mechanical properties. The results show that the increase of stretching temperature leads to the diffusion and regular stacking rate of BOPA6 chain segments towards crystal nuclei increases, the relative crystallinity increases, reaching 27.87% at 180 °C, and the mechanical strength and optical performance decrease. Heat-induced crystallization promotes the transformation of β-crystals to α-crystals in BOPA6, resulting in a more perfect crystalline structure and enhancing oxygen barrier properties. BOPA6 chains are oriented, and strain-induced crystallization (SIC) occurs during the biaxial stretching. Further increasing the stretch ratio, the relative crystallinity increased to 30.34%. The machine direction (MD) and transverse direction (TD) tensile strength of BOPA6 (B-33) are nearly two times higher than the unstretched film, reaching 134.33 MPa and 155.28 MPa, respectively. In addition, the permeation decreases to 57.61 cc·mil/(m day), and the oxygen barrier performance has improved by nearly 30% compared to the sample B-22. BOPA6 has a high storage modulus at a high stretching rate (300%/s). Rapid chain relaxation would promote the molecular chain disorientation, destroy the entangled network of the molecular chain, and lead to a decrease in tensile strength, reducing to about 110 MPa.