Designing bijels formed by solvent transfer induced phase separation with functional nanoparticles

Stephen Boakye-Ansah*, Matthew S. Schwenger, Martin F. Haase

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Bicontinuous interfacially jammed emulsion gels (bijels) formed via solvent transfer induced phase separation (STrIPS) are new soft materials with potential applications in separations, healthcare, or catalysis. To facilitate their applications, means to fabricate STrIPS bijels with nanoparticles of various surface chemistries are needed. Here, we investigate the formation of STrIPS bijels with nanoparticles of different wettabilities, ranging from partially hydrophobic to extremely hydrophilic. To this end, the surface wettability of silica nanoparticles is tailored by functionalization with ligands bearing either hydrophobic or hydrophilic terminal groups. We show that partially hydrophobic particles with acrylate groups can impart short-term stability to STrIPS bijels on their own. However, to enable long-term stability, the use of cationic surfactants is needed. Partially hydrophobic particles require short chain surfactants for morphological stability while glycerol-functionalized hydrophilic particles require double chain cationic surfactants. Variation of the surfactant concentration results in various STrIPS bijel morphologies with controllable domain sizes. Last, we show that functional groups on the nanoparticles facilitate interfacial cross-linking for the purposes of reinforcing STrIPS bijels. Our research lays the foundation for the use of a wide variety of solid particles, irrespective of their surface wettabilities, to fabricate bijels with potential applications in Pickering interfacial catalysis and as cross-flow microreactors.

Original languageEnglish
Pages (from-to)3379-3388
Number of pages10
JournalSoft Matter
Volume15
Issue number16
DOIs
Publication statusPublished - 2019
Externally publishedYes

Bibliographical note

Funding Information:
Acknowledgement is made to the National Science Foundation for support of this research under award number 1751479. This work was supported by NSF-CAREER award number 1751479.

Publisher Copyright:
© 2019 The Royal Society of Chemistry.

Funding

Acknowledgement is made to the National Science Foundation for support of this research under award number 1751479. This work was supported by NSF-CAREER award number 1751479.

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