摩尔质量
材料科学
共聚物
热塑性弹性体
聚合物
热塑性塑料
弹性体
复合材料
流变学
化学工程
高分子科学
高分子化学
工程类
作者
Jiuyang Zhang,Tuoqi Li,Alexander M. Mannion,Deborah K. Schneiderman,Marc A. Hillmyer,Frank S. Bates
出处
期刊:ACS Macro Letters
[American Chemical Society]
日期:2016-03-04
卷期号:5 (3): 407-412
被引量:105
标识
DOI:10.1021/acsmacrolett.6b00091
摘要
Fully sustainable poly[HPMC-g-(PMVL-b-PLLA)] graft block copolymer thermoplastics were prepared from hydroxypropyl methylcellulose (HPMC), β-methyl-δ-valerolactone (MVL), and l-lactide (LLA) using a facile two-step sequential addition approach. In these materials, rubbery PMVL functions as a bridge between the semirigid HPMC backbone and the hard PLLA end blocks. This specific arrangement facilitates PLLA crystallization, which induces microphase separation and physical cross-linking. By changing the backbone molar mass or side chain composition, these thermoplastic materials can be easily tailored to access either plastic or elastomeric behavior. Moreover, the graft block architecture can be utilized to overcome the processing limitations inherent to linear block polymers. Good control over molar mass and composition enables the deliberate design of HPMC-g-(PMVL-b-PLLA) samples that are incapable of microphase separation in the melt state. These materials are characterized by relatively low zero shear viscosities in the melt state, an indication of easy processability. The simple and scalable synthetic procedure, use of inexpensive and renewable precursors, and exceptional rheological and mechanical properties make HPMC-g-(PMVL-b-PLLA) polymers attractive for a broad range of applications.
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