Isotope Effects on the Crystallization Kinetics of Selectively Deuterated Poly(ε-Caprolactone)
- South China Univ. of Technology, Guangzhou (China). The Key Lab. of Polymer Processing Engineering of Ministry of Education; Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science; Univ. of Tennessee, Knoxville, TN (United States). Dept. of Chemical and Biomolecular Engineering
- Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science
- Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Neutron Scattering Division
- Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science; Univ. of Tennessee, Knoxville, TN (United States). Dept. of Materials Science and Engineering
- Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science and Neutron Scattering Division
- South China Univ. of Technology, Guangzhou (China). The Key Lab. of Polymer Processing Engineering of Ministry of Education;
- Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States). Center for Nanophase Materials Science; Univ. of Tennessee, Knoxville, TN (United States). Dept. of Chemical and Biomolecular Engineering
ABSTRACT Deuterium labeling of semi‐crystalline polymers can dramatically affect their crystallization behaviors. However, the influence of different labeled positions in a partially deuterated polymer on its crystallization is still far from understood. Here, we synthesized a series of selectively deuterated poly(ε‐caprolactones) (PCLs) through ring‐opening polymerization of ε‐caprolactone with controlled deuteration sites, including fully protiated (D0), fully deuterated (D10), tetra deuteration at the 3‐ and 7‐ caprolactone ring positions (D4) and hexa deuteration at the 4‐, 5‐, and 6‐ caprolactone ring positions (D6). All the PCLs showed a similar lamellar structure and parameters. Differential scanning calorimetry (DSC) analysis revealed that the equilibrium melting temperature , melting temperature T m , crystallization temperature T c , and crystallization kinetics changed systemically with the deuterium content except for D4, which indicates that the presence of CD 2 moieties on either side of ester group in the polymer chain combined with isotopic inhomogeneity could influence the chain packing. The nonmonotonic trend of T m as a function of deuterium content could be attributed to the difference in a hydrogen‐bond like intermolecular interaction between different PCLs. Partially deuterated PCLs (D4 and D6) showed an Avrami index near 2. After analyzing the parameters at the same supercooling temperature ΔT c , the existence of two crystallization regimes of PCLs were detected. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2019 , 57 , 771–779
- Research Organization:
- Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
- Sponsoring Organization:
- USDOE
- Grant/Contract Number:
- AC05-00OR22725
- OSTI ID:
- 1550757
- Alternate ID(s):
- OSTI ID: 1507187
- Journal Information:
- Journal of Polymer Science. Part B, Polymer Physics, Vol. 57, Issue 12; ISSN 0887-6266
- Publisher:
- WileyCopyright Statement
- Country of Publication:
- United States
- Language:
- English
Web of Science
Similar Records
Alternating crystalline lamellar structures from thermodynamically miscible poly(ε-caprolactone) H/D blends
Non-isothermal Crystallization and Degradation Kinetics of Fe{sub 3}O{sub 4}–Thymolblue Functionalized Poly(ε-caprolactone)