Automated parallel anionic polymerizations: Enhancing the possibilities of a widely used technique in polymer synthesis

被引:32
作者
Guerrero-Sanchez, C
Abeln, C
Schubert, US
机构
[1] Eindhoven Univ Technol, Lab Macromol Chem & Nanosci, NL-5600 MB Eindhoven, Netherlands
[2] Dutch Polymer Inst, NL-5600 MB Eindhoven, Netherlands
关键词
activation energy; anionic living polymerization; automated parallel synthesis; block copolymers; high-throughput experimentation; kinetic measurements for polymerizations; synthesis;
D O I
10.1002/pola.20887
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Anionic polymerization techniques have been implemented successfully in a commercial automated synthesizer. The main problems for a successful adaptation of the experimental technique in the automated synthesizer are addressed, as well as some simple potential applications, such as the anionic polymerization of styrene, isoprene, and methyl methacrylate. The obtained results were reproducible and in concordance with literature knowledge. The apparent rate constant of the anionic polymerization of styrene in cyclohexane initiated by sec-butyllithium could be determined at two different concentrations of the monomer and initiator in a temperature range of 10-60 degrees C. All the synthesis and characterization experiments of the polymers were performed within a short time period. Moreover, the syntheses of poly (styrene-b-isoprene) and poly(styrene-b-methyl methacrylate) block copolymers were also successfully carried out within the automated synthesizer. (c) 2005 Wiley Periodicals, Inc.
引用
收藏
页码:4151 / 4160
页数:10
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