Neutron Scattering Analysis of Water’s Glass Transition and Micropore Collapse in Amorphous Solid Water

The question of the nature of water’s glass transition has continued to be disputed over many years. Here we use slow heating scans (0.4 K min−1) of compact amorphous solid water deposited at 77 K and an analysis of the accompanying changes in the small-angle neutron scattering signal, to study mesoscale changes in the ice network topology. From the data we infer the onset of rotational diffusion at 115 K, a sudden switchover from nondiffusive motion and enthalpy relaxation of the network at 121 K, in excellent agreement with the glass transition onset deduced from heat capacity and dielectric measurements. This indicates that water’s glass transition is linked with long-range transport of water molecules on the time scale of minutes and, thus, clarifies its nature. Furthermore, the slow heating rates combined with the high crystallization resistance of the amorphous sample allow us to identify the glass transition end point at 136 K, which is well separated from the crystallization onset at 144 K—in contrast to all earlier experiments in the field

Association and liquid structure of pyridine-acetic acid mixtures determined from neutron scattering using a ‘free proton’ EPSR simulation model

Hydrogen-bonded molecular acetic acid chains are observed in acid–base mixtures from small angle neutron diffraction.</p

Bulk and Confined Benzene-Cyclohexane Mixtures Studied by an Integrated Total Neutron Scattering and NMR Method

From Springer Nature via Jisc Publications RouterHistory: accepted 2021-04-10, registration 2021-04-10, pub-electronic 2021-04-23, online 2021-04-23, pub-print 2021-08Publication status: PublishedFunder: Engineering and Physical Sciences Research Council; doi: http://dx.doi.org/10.13039/501100000266; Grant(s): N008995, N009304Abstract: Herein mixtures of cyclohexane and benzene have been investigated in both the bulk liquid phase and when confined in MCM-41 mesopores. The bulk mixtures have been studied using total neutron scattering (TNS), and the confined mixtures have been studied by a new flow-utilising, integrated TNS and NMR system (Flow NeuNMR), all systems have been analysed using empirical potential structure refinement (EPSR). The Flow NeuNMR setup provided precise time-resolved chemical sample composition through NMR, overcoming the difficulties of ensuring compositional consistency for computational simulation of data ordinarily found in TNS experiments of changing chemical composition—such as chemical reactions. Unique to the liquid mixtures, perpendicularly oriented benzene molecules have been found at short distances from the cyclohexane rings in the regions perpendicular to the carbon–carbon bonds. Upon confinement of the hydrocarbon mixtures, a stronger parallel orientational preference of unlike molecular dimers, at short distances, has been found. At longer first coordination shell distances, the like benzene molecular spatial organisation within the mixture has also found to be altered upon confinement

Under Pressure: The Structure of Water in Compressed Aqueous Trimethylamine N-Oxide - dataset

The following data are produced by using “empirical potential structure refinement” (EPSR) to analyse neutron scattering data on pressurised water and aqueous trimethylamine N-oxide. Experimental data are corrected for multiple scattering, attenuation, and inelasticity effects prior to EPSR. This produces a simulated box of atoms whose structure is consistent with the corrected experimental scattering data. This box is further analysed using custom analysis routines provided to calculate hydrogen bonding interaction energies between pairs of molecules

Solubility study of tobramycin in room temperature ionic liquids: an experimental and computational based study

Herein, we present a computational and experimental study assessing the solubility of tobramycin1in a series of hydrophilic room temperature ionic liquids (RTIL).</p

Small-angle neutron scattering study of micropore collapse in amorphous solid water

Vapor-deposited amorphous solid water (ASW) is the most abundant solid molecular material in space, where it plays a direct role in both the formation of more complex chemical species and the aggregation of icy materials in the earliest stages of planet formation. Nevertheless, some of its low temperature physics such as the collapse of the micropore network upon heating are still far from being understood. Here we characterize the nature of the micropores and their collapse using neutron scattering of gram-quantities of D2O–ASW of internal surface areas up to 230 ± 10 m2 g-1 prepared at 77 K. The model-free interpretation of the small-angle scattering data suggests micropores, which remain stable up to 120–140 K and then experience a sudden collapse. The exact onset temperature to pore collapse depends on the type of flow conditions employed in the preparation of ASW and, thus, the specific surface area of the initial deposit, whereas the onset of crystallization to cubic ice is unaffected by the flow conditions. Analysis of the small-angle neutron scattering signal using the Guinier–Porod model suggests that a sudden transition from three-dimensional cylindrical pores with 15 Å radius of gyration to two-dimensional lamellae is the mechanism underlying the pore collapse. The rather high temperature of about 120–140 K of micropore collapse and the 3D-to-2D type of the transition unraveled in this study have implications for our understanding of the processing and evolution of ices in various astrophysical environments