Abstract

In this study, a long carbon chain dimer acid is introduced into a nylon 6 structure and is copolymerized with different structural amines to produce amorphous nylon 6 by 4,4′-methylenebis(2-methylcyclohexylamine) (MMCA) in different copolymerization ratios. The effect of different structures and copolymerization ratios on the properties of nylon 6 is determined, along with the thermal properties, crystallinity, water absorption, dynamic mechanical properties, and optical properties. It is found that the melting point and the thermal cracking temperature Td10 of nylon 6 are respectively between 176 °C and 213 °C and 378 °C to 405 °C. The effect of introducing a bicyclohexane group containing a methyl side chain is greater than that of a meta-benzene ring, so COMM (synthesized by Caprolactam (C), dimer oleic acid (OA), and 4,4′-Methylenebis(2-methylcyclohexylamine) (MMCA)) has the lowest melting point, enthalpy, and crystallinity. As the copolymerization ratio increases, its thermal properties decrease. 10% is the lowest crystallinity. The amine structure containing a bicycloalkyl group has lower water absorption and a 10% copolymerization ratio gives the lowest water absorption. It contains the bicycloalkyl group, COM (synthesized by Caprolactam (C), dimer oleic acid (OA) and 4,4′-Methylenebis(cyclohexylamine) (MCA)), which has the highest loss modulus. The lowest loss modulus is noted for a copolymerization ratio of 7% and the value of tan δ increases as the copolymerization ratio increases. The introduction of nylon 6 with the bicycloalkyl groups, COMM and COM, significantly increases transparency. As the copolymerization ratio increases, the transparency increases and the haze decreases. The best optical properties are achieved for 10% copolymerization.

Highlights

  • Nylon 6 prepared by ring-opening polymerization of caprolactam is a common engineering polymer material

  • C: Caprolactam(CPL) and O: dimer oleic acid(OA)were obtained from commercial sources and purified by recrystallization

  • A ring-opening polymerization reaction for caprolactam is used and a dimer acid is copolymerized with different structural amines, to produce a series of non-crystalline nylon 6

Read more

Summary

Introduction

Nylon 6 prepared by ring-opening polymerization of caprolactam is a common engineering polymer material. It has excellent properties, such as good chemical resistance, high mechanical properties, and high thermal stability. It is processed and is has been widely used in automotive, textile, packaging, biomedical applications, and solar cells. Nylon 6 has excellent mechanical properties, good heat resistance, wear resistance and chemical solvent, and is very processed, the structure has a mercapto group so the hydrophilic group generates hydrogen bonds with. Dimensional changes occur when the material absorbs water, so the dimensional stability of the product is reduced. The tensile strength and bending strength decrease as the moisture absorption rate increases, which affects other properties of the product [1,2]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call