Controlled Epoxidation of Poly(styrene-b-isoprene-b-styrene) Block Copolymer for the Development of Nanostructured Epoxy Thermosets

GARATE, HERNAN; MONDRAGON IÑAKI,; GOYANES, SILVIA; D'ACCORSO, NORMA

JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY

JOHN WILEY & SONS INC

Año: 2011 vol. 40 p. 4505 - 4513

0887-624X

To be used as templates for nanostructured thermosets, a commercial poly(styrene-b-isoprene-b-styrene) (SIS) block copolymer (BCP) was epoxidized by three different epoxidation procedures. An exhaustive analysis of methodologies using metal catalyzed/hydrogen peroxide, dimethyldioxirane (DMDO), and meta-chloroperbenzoic acid (m-CPBA) was performed to obtain reactive BCPs. The DMDO approach was the best strategy to obtain highly epoxidized SIS BCP (85 mol %) without formation of side products. Careful control in BCP epoxidation by metal catalyzed/hydrogen peroxide and m-CPBA approaches led to a maximum epoxidation degree (ED) of approximately 60 mol % without the formation of side products. The ED by metal catalyzed/hydrogen peroxide strategy could be further increased to 69 mol %, but a significant amount of cross-linking, ring opening, and polymer chain scission reactions were detected by spectroscopic and chromatographic techniques. The miscibility of epoxidized BCPs with diglycidyl ether of bisphenol-A epoxy system before and after curing was analyzed to develop nanostructured epoxy thermosets. For ED higher than 69 mol %, BCPs were miscible, while those with lower ED presented macrophase separation. Highly epoxidized BCPs obtained by the DMDO methodology were successfully used to obtain ordered nanodomains inside the epoxy matrix, as determined by atomic force microscopy