This document lays out a set of near-future investigations in salt, the third phase of BATS (BATS 3). This phase is planned to answer the few remaining issues from the first two phases of BATS (BATS 1 and BATS 2), and to prepare for a subsequent large-scale demonstration phase. The BATS experiments are the first part of a larger plan to conduct field experiments to answer specific technical questions, improve the technical basis for disposal of heat-generating radioactive waste in salt (Stauffer et al., 2015; SNL et al., 2020), and demonstrate readiness for disposal of radioactive waste in salt, including large, hot waste packages.
Glycoboehmite (GB) materials are synthesized by a solvothermal reaction to form layered aluminum oxyhydroxide (boehmite) modified by intercalated butanediol molecules. These hybrid materials offer a platform to design materials with potentially novel sorption, wetting, and catalytic properties. Several synthetic methods have been used, resulting in different structural and spectroscopic properties, but atomistic detail is needed to determine the interlayer structure to explore the synthetic control of GB materials. Here, we use classical molecular dynamics (MD) simulations to compare the structural properties of GB interlayers containing chemisorbed butanediol molecules as a function of diol loading. Accompanying quantum (density functional theory, DFT) static calculations and MD simulations are used to validate the classical model and compute the infrared spectra of various models. Classical MD results reveal the existence of two unique interlayer environments at higher butanediol loading, corresponding to smaller (cross-linked) and expanded interlayers. DFT-computed infrared spectra reveal the sensitivity of the aluminol O-H stretch frequencies to the interlayer environment, consistent with the spectrum of the synthesized material. Insight from these simulations will aid in the characterization of the newly synthesized GB materials.