On the Versatility of Urethane/Urea Bonds: Reversibility, Blocked Isocyanate, and Non-isocyanate Polyurethane

被引:1029
作者
Delebecq, Etienne [1 ]
Pascault, Jean-Pierre [2 ,3 ]
Boutevin, Bernard [1 ]
Ganachaud, Francois [1 ,2 ,3 ]
机构
[1] Ecole Natl Super Chim Montpellier, Inst Charles Gerhardt, CNRS, UMR 5253, F-34296 Montpellier 05, France
[2] INSA Lyon, IMP, UMR5223, F-69621 Villeurbanne, France
[3] Univ Lyon, F-69622 Villeurbanne, France
关键词
RING-OPENING POLYMERIZATION; CARBONATE FUNCTIONAL POLYMERS; ISOPROPENYL BENZYL ISOCYANATE; 5-MEMBERED CYCLIC CARBONATE; LIQUID-PHASE REACTIONS; THERMAL-DISSOCIATION; PHENYL ISOCYANATE; ARYL ISOCYANATES; SYNCHROTRON SAXS; MOLECULAR-ORGANIZATION;
D O I
10.1021/cr300195n
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The approach of the reversibility of isocyanate-based bond to all products of isocyanate chemistry, namely, urethane, urea, uretdione, biuret, allophanate, and isocyanurate, is reviewed. The high reactivity of the isocyanate group toward any nucleophilic compound promotes its reaction with both the reactant and the formed product from isocyanate/nucleophile reaction, if it is sufficiently nucleophilic. To obtain TP or cast PU elastomers, one or two diols can be reacted with the isocyanate. Phase separation is the essential parameter for controlling the final thermomechanical behavior for linear segmented TPU. These polymers offer unique possibilities for tailor-made materials through the variation of the block lengths and composition. Because isocyanate/alcohol and isocyanate/amine reactions are very fast, give no byproduct, and attain high degree of conversion, they are well suited for direct polymerization of two reactive liquids, A and B, in a mold.
引用
收藏
页码:80 / 118
页数:39
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