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Neutron diffraction with H/D isotopic substitution is used to investigate the structure of low density amorphous ice produced from (1) high density amorphous ice by isobaric warming and (2) very high density amorphous ice by isothermal decompression. Differences are found in the scattering patterns of the two low density amorphous ices that correlate with structural perturbations on intermediate length scales in the hydrogen bonded water network. Atomistic modeling suggests that the structural states of the two samples may relate to a competition between short range and intermediate range order and disorder. This structural difference in two low density amorphous (LDA) ices is also evident when comparing their compression behavior. In terms of the energy landscape formalism this finding implies that we have produced and characterized the structural difference of two different basins within the LDA-megabasin corresponding to identical macroscopic densities. [ABSTRACT FROM AUTHOR]

Using isotope substitution neutron scattering data, we present a detailed structural analysis of the short and intermediate range structures of the five known forms of amorphous ice. Two of the lower density forms—amorphous solid water and hyperquenched glassy water—have a structure very similar to each other and to low density amorphous ice, a structure which closely resembles a disordered, tetrahedrally coordinated, fully hydrogen bonded network. High density and very high density amorphous ices retain this tetrahedral organization at short range, but show significant differences beyond about 3.1 Å from a typical water oxygen. The first diffraction peak in all structures is seen to be solely a function of the intermolecular organization. The short range connectivity in the two higher density forms is more homogeneous, while the hydrogen site disorder in these forms is greater. The low Q behavior of the structure factors indicates no significant density or concentration fluctuations over the length scale probed. We conclude that these three latter forms of ice are structurally distinct. Finally, the x-ray structure factors for all five amorphous systems are calculated for comparison with other studies. [ABSTRACT FROM AUTHOR]

Salting out of amphiphiles from aqueous solution is a process of central importance in aqueous solution chemistry and of major application in the concentration of macromolecules and the crystallization of proteins. Despite its importance, our understanding of the mechanism is poor, there being no direct experimental evidence to support the several competing explanations in the literature. Using neutron diffraction with isotope substitution, we report a structural study of the effect of adding a simple salting out agent (NaCl) to a dilute solution of an amphiphile (t-butanol). The results show clearly that the anion is central to driving the changes in association of the amphiphile through the formation of an anion bridge between the polar ends of neighboring alcohol molecules. This further exposes the nonpolar surface of the amphiphile and suggests that further association may then occur through hydrophobic interaction. The mechanism uncovered is both different from those currently in the literature and relatively simple, and offers a possible route forward to understanding the variation in salting out efficacy of different ions as indicated by the Hofmeister or lyotropic series. © 2003 American Institute of Physics. [ABSTRACT FROM AUTHOR]

The structure of a 0.86 mole fraction solution of tertiary butanol in water at room temperature has been investigated by neutron diffraction with hydrogen/deuterium isotope substitution. The intermolecular correlations between the alcohol and water molecules have been extracted using the empirical potential structure refinement technique. The results highlight the creation of water pockets within the solution structure. These pockets mediate the interactions that occur between the alcohol hydroxyl groups, reducing the level of direct alcohol-alcohol hydrogen bonding. The results show that only a small amount of water is required to drive this solution in the direction of hydrophobic behavior more commonly associated with the water-rich solution compositions. [ABSTRACT FROM AUTHOR]

NIMROD is the Near and InterMediate Range Order Diffractometer of the ISIS second target station. Its design is optimized for structural studies of disordered materials and liquids on a continuous length scale that extends from the atomic, upward of 30 nm, while maintaining subatomic distance resolution. This capability is achieved by matching a low and wider angle array of high efficiency neutron scintillation detectors to the broad band-pass radiation delivered by a hybrid liquid water and liquid hydrogen neutron moderator assembly. The capabilities of the instrument bridge the gap between conventional small angle neutron scattering and wide angle diffraction through the use of a common calibration procedure for the entire length scale. This allows the instrument to obtain information on nanoscale systems and processes that are quantitatively linked to the local atomic and molecular order of the materials under investigation. [ABSTRACT FROM AUTHOR]

Energy-dispersive X-ray absorption spectroscopy is an increasingly powerful tool for the investigation of kinetic processes in chemical systems as an element-specific local structure and electronic-state probe. Advances in synchrotron radiation sources and detector technology are pushing the time resolution of the method to ever shorter periods, currently milliseconds to microseconds, while also providing a concomitant improvement in data quality that now makes feasible the identification of structural and electronic motifs characteristic of intermediate states in chemical processes. To maximize the value of the newly available high-quality time-resolved data, techniques for consistent data normalization and structural component analysis have been developed and here are illustrated in a model study of the electron-transfer reaction between [IrCl6]2- with [Co(CN)5]3-. [ABSTRACT FROM AUTHOR]

The development of third-generation synchrotron radiation sources has created considerable opportunities for the investigation of systems under extreme sample conditions of pressure and temperature. This paper presents the application of a recently developed pressure cell and pressurization and circulation system to the investigation of the hydrophobic hydration of noble gases by X-ray absorption spectroscopy. This system operates in the pressure range from 1 bar to 1 kbar, and allows for mixing of gaseous and liquid components and the control of the ultimate gas in liquid concentration. First results demonstrate the remarkable resilience of the first hydration shell of a nonpolar solute (krypton) to the application of pressure in the 150 bar to 700 bar range. These results suggest questioning the conclusions of some recent computer simulations, in particular with regards to the potential impact of such studies on our understanding of pressure induced protein denaturation. [ABSTRACT FROM AUTHOR]

It is no accident that the start of the 21st century has seen significant growth in the field of nanotechnology across all the sciences. The nanoscale is the realm of the molecule, where physics, chemistry and biology meet, and where the potential for engineering control of structures containing tens to thousands of atoms is just beginning to be realised. Myriad examples of nanotechnology's existing and potential impact range from the creation of new designer drugs, through the development of hydrogen storage materials, to state-of-the-art silicon technology. This is the science that underpins the rationale for the construction of the near and intermediate range order diffractometer, Nimrod, on the ISIS second target station. [ABSTRACT FROM AUTHOR]

Hydrogen/deuterium isotopic substitution neutron diffraction techniques have been used to measure the solute-solute, solute-solvent and solvent-solvent structural correlation functions in a 0.06 mole fraction solution of tertiary butanol in water. The measurements were made at two temperatures, 25 °C and 65 °C. Data analysis to the level of intermolecular orientational correlation functions was performed by the Empirical Potential Structure Refinement (EPSR) technique in combination with a spherical harmonic coefficient analysis. The results reveal in particular a subtle temperature dependence of the intermolecular structure of the solvent water. This structural perturbation is suggestive of a hydrophobic hydration induced, local density enhancement in the solvent water that could relate to the entropic driving force underlying the hydrophobic interaction mechanism. © 2001 American Institute of Physics. [ABSTRACT FROM AUTHOR]

Presents an erratum on the study concerning the structure of pure tertiary butanol. Reproduction of the corrected figures; Use of spherical harmonic formalism to extract intermolecular correlations between the two models; Accounts of hydrogen bond interactions in the fixed potential model system.

The phase behavior of sorbed CO2 in an ordered mesoporous silica sample (SBA-15) was studied by neutron diffraction. Surprisingly, upon cooling our sample below the bulk critical point, confined CO2 molecules neither freeze nor remain liquid as expected, but escape from the pores. The phenomenon has additionally been confirmed gravimetrically. The process is reversible and during heating CO2 refills the pores, albeit with hysteresis. This depletion was for the first time observed in an ordered mesoporous molecular sieve and provides new insight on the phase behavior of nanoconfined fluids. [ABSTRACT FROM AUTHOR]