Chain arrangements of selectively deuterated poly(ε-caprolactone) copolymers as revealed by neutron scattering

Lengwan Li, Tianyu Li, Matthias M.L. Arras, Peter V. Bonnesen, Xiangfang Peng, Wei Li, Kunlun Hong

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4 Scopus citations

Abstract

The chain arrangement within the crystalline lamellae has been the focus of polymer crystallization. In this study, a series of protiated (H) and deuterated (D) poly(ε-caprolactone) (PCL) blends, block and random copolymers were investigated by small-angle neutron scattering (SANS) measurements. The spatial inhomogeneities of block copolymers were analyzed via Debye-Bueche method and temperature dependence of Flory-Huggins interaction parameter χ in the melt was extracted from fitting the scattering data to the random phase approximation model. Studying the changes of SANS signals further revealed that the copolymers exhibit cooling rate-dependent crystallization behaviors. A unique SANS double-peak pattern was found in D4/D10 50/50 blend and D10-D0-D10 triblock copolymers (where D0, D4, and D10 indicate PCL with different levels of deuteration), as a result of two types of contrasts: scattering length density (SLD) difference between lamellae of different components and density difference between amorphous and lamellar domains. These detailed findings complement our understanding of the complex crystallization processes of deuterated polyesters, which also suggest an avenue for fine control of crystal structures that adds to materials design.

Original languageEnglish
Article number122375
JournalPolymer
Volume193
DOIs
StatePublished - Apr 10 2020

Funding

The polymers were synthesized at the Center for Nanophase Materials Sciences (CNMS) at the Oak Ridge National Laboratory (ORNL), which is a DOE Office of Science User Facility. Neutron scattering studies were performed at the CG-3 Bio-SANS instrument at the High-Flux Isotope Reactor (HFIR), ORNL, which is sponsored by the Office of Biological and Environmental Research , and the Scientific User Facilities Division , Office of Basic Energy Sciences, U.S. Department of Energy . This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357 . L. Li thanks the Chinese Scholarship Council for financial support. The polymers were synthesized at the Center for Nanophase Materials Sciences (CNMS) at the Oak Ridge National Laboratory (ORNL), which is a DOE Office of Science User Facility. Neutron scattering studies were performed at the CG-3 Bio-SANS instrument at the High-Flux Isotope Reactor (HFIR), ORNL, which is sponsored by the Office of Biological and Environmental Research, and the Scientific User Facilities Division, Office of Basic Energy Sciences, U.S. Department of Energy. This research used resources of the Advanced Photon Source, a U.S. Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357. L. Li thanks the Chinese Scholarship Council for financial support.

Keywords

  • Crystallization
  • Deuterated PCL copolymers
  • SANS

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