期刊论文详细信息
POLYMER 卷:193
Chain arrangements of selectively deuterated poly(ε-caprolactone) copolymers as revealed by neutron scattering
Article
Li, Lengwan1,3,4  Li, Tianyu1  Arras, Matthias M. L.2,5  Bonnesen, Peter, V1  Peng, Xiangfang3  Li, Wei1  Hong, Kunlun1,4 
[1] Oak Ridge Natl Lab, Ctr Nanophase Mat Sci, POB 2009, Oak Ridge, TN 37831 USA
[2] Oak Ridge Natl Lab, Neutron Scattering Div, POB 2009, Oak Ridge, TN 37831 USA
[3] South China Univ Technol, Key Lab Polymer Proc Engn, Minist Educ, Guangzhou 510640, Peoples R China
[4] Univ Tennessee, Dept Chem & Biomol Engn, Knoxville, TN 37996 USA
[5] Mat Sci Ctr, DSM, Urmonderbaan 22, NL-6167 RD Geleen, Netherlands
关键词: Crystallization;    SANS;    Deuterated PCL copolymers;   
DOI  :  10.1016/j.polymer.2020.122375
来源: Elsevier
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【 摘 要 】

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(e-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. 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.

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