Thermoplastic polyacetals: chemistry from the past for a sustainable future?

被引:74
|
作者
Hufendiek, Andrea [1 ]
Lingier, Sophie [1 ]
Du Prez, Filip E. [1 ]
机构
[1] Univ Ghent, Dept Organ & Macromol Chem, Polymer Chem Res Grp, Ctr Macromol Chem CMaC, Krijgslaan 281 S4 Bis, B-9000 Ghent, Belgium
关键词
RING-OPENING POLYMERIZATION; SOLID-STATE MODIFICATION; DRUG-DELIVERY; HYPERBRANCHED POLYACETALS; POLYKETAL MICROPARTICLES; CATIONIC-POLYMERIZATION; ALIPHATIC POLYESTERS; AROMATIC POLYAMIDES; COPOLYMER MICELLES; ACID;
D O I
10.1039/c8py01219a
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Synthetic thermoplastic polyacetals have a long history dating back to 1912. While polymers with non-cyclic acetal repeat units are typically well soluble and degrade easily at biologically relevant pH values, polycycloacetals have a rigid polymer backbone, resulting in favorable thermal and mechanical properties but are often insoluble and thus challenging to process. In recent years, the degradation behavior and the availability of many building blocks from renewable resources have sparked renewed interest in poly(cyclo)acetals. This review provides a critical overview over the synthetic routes to polyacetals, highlighting where possible the material properties. Direct polyacetalization and polytransacetalization techniques are discussed first, followed by the polymerization of acetal containing monomers and recent ring opening polymerization approaches. Thermoplastic polyacetals show promise in delivery applications but also as bulk materials, where a combination of excellent material properties, a potential for renewable sourcing and degradation as an end-of-life option are of ever increasing importance.
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页码:9 / 33
页数:25
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