Determining soft segment structure-property effects in the enhancement of segmented polyurethane performance

Liquid Crystalline Elastomer (LCE)-inspired segmented polyurethane elastomers possessing widely different extents of ordering were created to mimic the hierarchical structure of the continuous matrix and superior mechanical performance of spider silk fibers. The silk's remarkable toughness originates from a fiber morphology that possesses [beta]-pleated crystalline sheets within an amorphous matrix. In the polyurethane materials, various extents of poly(ethylene oxide) (PEO) soft segment ordering were implemented within continuous soft domains that were connected by hexamethylene diisocyanate-butanediol (HDI-BDO) hard segments. Soft segment crystallinity studies revealed the need to optimize the extent of continuous soft domain ordering. Highly crystalline PEO soft segments, while they display good microphase segregation properties, sacrifice extensibility due to their high melting transition temperature. Moderately crystalline PEO soft segments, meanwhile, possess less defined phase segregation but enhanced mechanical properties from their reversible dispersed crystalline soft segment domains. Non-crystalline Pluronic copolymer systems had good mechanical properties that resulted from both a strong hard segment incompatibility and a highly mobile soft segment matrix. Hydrogen-bonded hard domain shearing during in-situ tensile deformation yields oriented hard blocks that align at a preferred tilt angle of ±60° from the strain direction. Extensive alignment and orientation of the moderately-ordered PEO soft segments occurred during deformation, which was consistent with its observed mechanical behavior. Pluronic-containing segmented polyurethanes formed an ordered mesophase in the continuous soft matrix during deformation. A series of cyclic, aliphatic polyurethanes with dicyclohexyl methane diisocyanate (HMDI) hard segments and poly(tetramethylene oxide) (PTMO) soft segments was synthesized to study compositional effects on the extent of soft segment mixing, and how these effects translated to both mechanical and barrier performance. Shorter soft segment chain systems displayed a greater hard segment compatibility, which resulted in materials that were both more rigid mechanically and provided better barrier characteristics.

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Chemical Engineering.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2009

Author dc:creator

• Waletzko, Ryan Scott

Advisor dc:contributor.advisor

• Paula T. Hammond.

• Chemical Engineering.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/46671

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/46671