Biodegradable amylose-g-PLA glycopolymers from renewable resources

被引:24
作者
Ouhib, Rachid [2 ]
Renault, Benjamin [1 ]
Mouaziz, Hanna [1 ]
Nouvel, Cecile [1 ]
Dellacherie, Edith [1 ]
Six, Jean-Luc [1 ]
机构
[1] Nancy Univ, LCPM, UMR CNRS INPL 7568, Grp ENSIC, F-54001 Nancy, France
[2] Univ Dj Liabes, Lab Chim Organ Phys & Macromol, Fac Sci, Fg Gambetta 22000, Sidi Bel Abbes, Algeria
关键词
Amylose; Starch; PLA; Grafted copolymer; Compatibilizer; PLASTICIZED STARCH; L-LACTIDE; RELATIVE REACTIVITIES; DIMETHYL-SULFOXIDE; HYDROXYL-GROUPS; CYCLIC ESTERS; POLYMERIZATION; SILYLATION; DEXTRAN; HEXAMETHYLDISILAZANE;
D O I
10.1016/j.carbpol.2008.11.038
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The synthesis of biodegradable PLA-grafted amylose copolymers has been achieved in three steps to control their architecture as best as possible. First, amylose was partially protected with various silylating agents, especially N,O-bis-(trimethylsilyl)acetamide (BSA). The influence of the silylating agent chemistry and of the BSA/OH molar ratio on the protection yield have been investigated. Furthermore, the reactivity order of the different OH functions towards silylation has been evaluated. The second step is based on the "grafting form" strategy: polylactide (PLA) grafts were generated by the Ring Opening Polymerization (ROP) of D,L-lactide from the free remaining OH groups carried by the partially silylated amylose. Finally, the silylether groups cleavage was tested under various conditions to obtain the PLA-grafted amylose (A-g-PLA), while avoiding backbone and grafts degradation. In addition, two polyelectrolytes, i.e., LiCl and NaNO3 have been used to facilitate the SEC analysis of native amylose. Crown Copyright (C) 2008 Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:32 / 40
页数:9
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