Combined Small-Angle Neutron Scattering, Diffusion NMR, and Molecular Dynamics Study of a Eutectogel: Illuminating the Dynamical Behavior of Glyceline Confined in Bacterial Cellulose Gels

Chip J. Smith, Durgesh V. Wagle, Nakara Bhawawet, Sascha Gehrke, Oldamur Hollóczki, Sai Venkatesh Pingali, Hugh O'Neill, Gary A. Baker

Research output: Contribution to journalArticlepeer-review

21 Scopus citations

Abstract

A deep eutectic solvent (DES) entrapped in a bacterial cellulose (BC) network gives rise to a gelatin-like, self-supported material termed a bacterial cellulose eutectogel (BCEG). Although this novel material holds potential for numerous industrial, environmental, energy, or medical applications, little is known about the structural features or dynamical behavior within a eutectogel. In this work, we employ X-ray diffraction (XRD), nuclear magnetic resonance (NMR), and small-angle neutron scattering (SANS) to probe the structural and diffusive behavior of the prevailing DES glyceline (1:2 molar ratio of choline chloride:glycerol) confined within bacterial cellulose. XRD investigations demonstrate that the bacterial cellulose maintains its crystallinity even as the glyceline content approaches 95 wt % in the BCEG, an outcome corroborated by molecular dynamics (MD) simulations, which suggest minimal changes in the structural features of the cellulose chains due to the presence of glyceline. SANS measurements reveal a significant reduction in the radius of gyration (Rg) for BC in a BCEG compared to its hydrogel analogue, indicating a collapse in the microfibrillar structure that we attribute to removal of waters from the interfibrillar space due to a higher affinity of DES for water than for cellulose. Furthermore, SANS experiments suggest that the vast majority of DES is hosted within large micropores in the BCEG (i.e., mesoscopic confinement). Interestingly, proton NMR experiments disclose faster diffusional rates for choline and glycerol entrapped in a BCEG compared to neat glyceline. MD simulations offer the possible explanation that this diffusional acceleration results from significant migration of chloride from the bulk to cellulose microfibrillar surfaces, thereby reducing hydrogen bonding with choline and glycerol partners. This study provides the first comprehensive investigation into the structure and diffusional dynamics of glyceline within a eutectogel, offering insights into mass transport that should be useful for tailoring these novel materials to potential applications.

Original languageEnglish
Pages (from-to)7647-7658
Number of pages12
JournalJournal of Physical Chemistry B
Volume124
Issue number35
DOIs
StatePublished - Sep 3 2020

Funding

This work was supported by the Research Corporation for Science Advancement (G.A.B.). C.J.S.II was supported by an IGERT trainee fellowship administered by the National Science Foundation (Grant No. DGE-1069091). SANS studies on Bio-SANS were supported by the Office of Biological and Environmental Research (OBER) funded Center for Structural Molecular Biology (CSMB) under Contract FWP ERKP291, using the High Flux Isotope Reactor supported by the Office of Basic Energy Sciences (BES), U.S. Department of Energy (DOE). The authors would also like to thank the University of Missouri-Columbia Nuclear Magnetic Resonance Core (Grant No. NSF DBI-0070359) for assistance with the NMR experiments.

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