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Title: Bicontinuous Microemulsions in Partially Charged Ternary Polymer Blends

Journal Article · · ACS Macro Letters

We describe the phase behavior of a partially charged ternary polymer blend model system, comprising a compositionally symmetric poly[(oligo(ethylene glycol) methyl ether methacrylate-co-oligo(ethylene glycol) propyl sodium sulfonate methacrylate)]-b-polystyrene (POEGMA23–PS) diblock polymer and the constituent POEGMA23 and PS homopolymers, along the volumetrically symmetric isopleth, where 23 denotes the percentage of charged monomers in the POEGMA chain. Small-angle neutron and X-ray scattering and dynamic mechanical spectroscopy measurements reveal morphological transitions from a layered superlattice to swollen lamellae to a bicontinuous microemulsion (BμE), followed by macroscopic phase separation, with increasing homopolymer content. The BμE channel occurs between 85 and 90% homopolymer addition, positioned approximately at the isotropic Lifshitz composition predicted by mean-field theory for neutral systems. The resulting BμE morphology exhibits a periodicity of 26 nm, yielding a mesoscopically structured but macroscopically disordered bicontinuous structure. That this structure can be achieved in a charged polymer system is surprising, given the huge asymmetries typically induced by adding charge to either diblock copolymers or binary polymer blends.

Research Organization:
Univ. of Minnesota, Twin Cities, MN (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
SC0017809
OSTI ID:
1831779
Journal Information:
ACS Macro Letters, Vol. 8, Issue 9; ISSN 2161-1653
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 14 works
Citation information provided by
Web of Science

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