Side-chain crystallization in alkyl-substituted cellulose esters and hydroxypropyl cellulose esters

被引:21
作者
Chen, Xi [2 ]
Zheng, Nan [1 ]
Wang, Qiao [1 ]
Liu, Lingzhi [1 ]
Men, Yongfeng [1 ]
机构
[1] Univ Chinese Acad Sci, Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Renmin St 5625, Changchun 130022, Peoples R China
[2] East China Jiaotong Univ, Sch Mat Sci & Engn, Nanchang 330013, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Cellulose esters; Hydroxypropyl cellulose esters; Side chain crystallization behavior; Phase transition behavior; X-RAY-SCATTERING; RIGID-ROD POLYMERS; TRANSITION-TEMPERATURES; NANOPHASE SEPARATION; GLASS-TRANSITION; PHASE-TRANSITION; CRYSTALLINITY; ORDER; HOMOPOLYMERS; DERIVATIVES;
D O I
10.1016/j.carbpol.2017.01.028
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The differences in side chain crystallization behavior between cellulose esters (CEs) and hydroxypropyl cellulose esters (HPCEs) were systematically investigated by a combination of differential scanning calorimetry (DSC) and small and wide-angle X-ray scattering techniques. DSC investigation indicated that under the same side chain length, the fusion enthalpy and the number of crystallized CH2 of CEs were smaller than HPCEs. At the same time, their d-spacing and molecular arrangements were also different from each other. For the CEs, the side chains are perpendicular to the main chain, while the side chains most probably tend to tilt to main chain in the HPCEs as was evidenced by X-ray scattering results. The phenomenon can be understood as a consequence of different flexibility of attachment bridges in both kinds of side chain polymers and the steric hindrance of methyl group in the hydroxypropyl group in HPCEs. In addition, the added hydroxypropyl substituents make the side chain length increasing. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:28 / 34
页数:7
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