Influence of Polymer Chain Architecture of Poly(vinyl alcohol) on the Inhibition of Ice Recrystallization

被引:33
|
作者
Olijve, Luuk L. C. [1 ,2 ]
Hendrix, Marco M. R. M. [3 ]
Voets, Ilja K. [1 ,2 ,3 ]
机构
[1] Eindhoven Univ Technol, Inst Complex Mol Syst, POB 513, NL-5600 MB Eindhoven, Netherlands
[2] Eindhoven Univ Technol, Lab Macromol & Organ Chem, POB 513, NL-5600 MB Eindhoven, Netherlands
[3] Eindhoven Univ Technol, Dept Chem Engn & Chem, POB 513, NL-5600 MB Eindhoven, Netherlands
基金
欧洲研究理事会;
关键词
controlled radical polymerization; ice recrystallization inhibition; polymer architecture; poly(vinyl alcohol); molecular bottlebrush; TRANSFER RADICAL POLYMERIZATION; RAFT POLYMERIZATION; BLOCK-COPOLYMERS; CLATHRATE WATERS; GLYCOPROTEINS; PROTEINS; ACETATE;
D O I
10.1002/macp.201500497
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(vinyl alcohol) (PVA) is a water-soluble synthetic polymer well-known to effectively block the recrystallization of ice. The effect of polymer chain architecture on the ice recrystallization inhibition (IRI) by PVA remains unexplored. In this work, the synthesis of PVA molecular bottlebrushes is described via a combination of atom-transfer radical polymerization and reversible addition-fragmentation chain-transfer polymerization. The facile preparation of the PVA bottlebrushes is performed via the selective hydrolysis of the chloroacetate esters of the poly(vinyl chloroacetate) (PVClAc) side chains of a PVClAc precursor bottlebrush. The IRI efficacy of the PVA bottlebrush is quantitatively compared to linear PVA. The results show that even if the PVA chains are densely grafted onto a rigid polymer backbone, the IRI activity of PVA is maintained, demonstrating the flexibility in PVA polymer chain architecture for the design of synthetic PVA-based ice growth inhibitors.
引用
收藏
页码:951 / 958
页数:8
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