TY - JOUR
T1 - Effects of epoxidation degree on strain-induced crystallization and mechanical properties of epoxidized natural rubber
AU - Wang, Zixuan
AU - Song, Han
AU - Wang, Ruoyu
AU - Zhang, Xi
AU - Yuan, Qipeng
AU - Lu, Yonglai
AU - Song, Weixiao
AU - Wu, Xiaohui
AU - Hu, Guo Hua
AU - Zhang, Liqun
N1 - Publisher Copyright:
© 2025
PY - 2025/8/13
Y1 - 2025/8/13
N2 - The epoxidation degree (ED) plays a critical role in shaping the microstructure and macroscopic performance of epoxidized natural rubber (ENR). Through the application of Synchrotron Radiation-Wide Angle X-ray Diffraction (SR-WAXD), polarized Fourier Transform Infrared (FTIR) spectroscopy, and Atomic Force Microscopy (AFM), the effects of different ED on the strain-induced crystallization (SIC) behavior, mechanical properties, and molecular chain orientation of ENRs were systematically investigated. The findings reveal that at a given strain there is an optimum ED with regard to crystallinity and mechanical performance. Notably, ENR10 (with an ED of 10 %) demonstrated the highest tensile strength of 30.8 MPa and tear strength of 35.9 kN/m, corresponding to improvements of 27.8 % and 40.2 %, respectively, compared to NR. The influence of the ED is most pronounced in the orientation and crystallite growth. For ENR with a low ED, epoxy groups enhance molecular chain orientation and SIC, facilitating the formation of more crystallites. The increased crystallite number allows for the rapid establishment of a crystallite network, promoting continuous crystallite growth and cross-linking. Consequently, significant increases in tensile and tear strength are observed. In contrast, ENR with a high ED reduced crystallite growth due to steric hindrance and increased interactions among the densely packed epoxy groups. This effect impairs crystallite formation and diminishes SIC capability, resulting in a notable decline in both crystallinity and mechanical properties.
AB - The epoxidation degree (ED) plays a critical role in shaping the microstructure and macroscopic performance of epoxidized natural rubber (ENR). Through the application of Synchrotron Radiation-Wide Angle X-ray Diffraction (SR-WAXD), polarized Fourier Transform Infrared (FTIR) spectroscopy, and Atomic Force Microscopy (AFM), the effects of different ED on the strain-induced crystallization (SIC) behavior, mechanical properties, and molecular chain orientation of ENRs were systematically investigated. The findings reveal that at a given strain there is an optimum ED with regard to crystallinity and mechanical performance. Notably, ENR10 (with an ED of 10 %) demonstrated the highest tensile strength of 30.8 MPa and tear strength of 35.9 kN/m, corresponding to improvements of 27.8 % and 40.2 %, respectively, compared to NR. The influence of the ED is most pronounced in the orientation and crystallite growth. For ENR with a low ED, epoxy groups enhance molecular chain orientation and SIC, facilitating the formation of more crystallites. The increased crystallite number allows for the rapid establishment of a crystallite network, promoting continuous crystallite growth and cross-linking. Consequently, significant increases in tensile and tear strength are observed. In contrast, ENR with a high ED reduced crystallite growth due to steric hindrance and increased interactions among the densely packed epoxy groups. This effect impairs crystallite formation and diminishes SIC capability, resulting in a notable decline in both crystallinity and mechanical properties.
KW - Epoxidized natural rubber
KW - Mechanical properties
KW - Molecular chain orientation
KW - Strain-induced crystallization
UR - https://www.scopus.com/pages/publications/105006826750
U2 - 10.1016/j.polymer.2025.128541
DO - 10.1016/j.polymer.2025.128541
M3 - 文章
AN - SCOPUS:105006826750
SN - 0032-3861
VL - 333
JO - Polymer
JF - Polymer
M1 - 128541
ER -