A neutron spin echo study of low-temperature water confined in the spherical silica pores of SBA-16.

The dynamic properties of heavy water (DO) and light water (HO) confined in porous silica SBA-16 were studied over a temperature range of 210-290 K by neutron spin echo measurements. SBA-16 has predominant spherical pores (7.1 nm in pore size), channels interconnecting the spherical pores, and micropores (corona).

Tubular nitrogen-doped TiO samples with efficient photocatalytic properties based on long-lived charge separation under visible-light irradiation: synthesis, characterization and reactivity.

A nitrogen-doped TiO sample was prepared at 413 K by direct hydrothermal treatment of titanium isopropoxide in an aqueous solution of NH. This new material has a large specific surface area of ca. 220 m g because of its tubular structure and it exhibits a prominent absorption feature in the region between 400 and 650 nm.

Different behavior of water in confined solutions of high and low solute concentrations.

Water-glycerol solutions confined in 21 Å pores of the silica matrix MCM-41 C10 have been studied using differential scanning calorimetry (DSC) and broadband dielectric spectroscopy (BDS). The results suggest a micro-phase separation caused by the confinement. Likely the water molecules coordinate to the hydroxyl surface groups of the pores, leaving most of the glycerol molecules in the centre of the pores.

Low temperature phase properties of water confined in mesoporous silica MCM-41: thermodynamic and neutron scattering study.

The phase properties of water confined in mesoporous silica MCM-41 were investigated over a temperature range of 100-298 K as a function of pore size by specific heat capacity and inelastic neutron scattering (INS) measurements. The water content of the samples was carefully controlled to ensure the capillary filled state and no overloading of water. The values of heat capacity of the pore water are higher than those of bulk ice and liquid water over the whole temperature range measured.

Highly compressed nanosolution restricted in cylindrical carbon nanospaces.

We shed light on the specific hydration structure around a zinc ion of nanosolution restricted in a cylindrical micropore of single-wall carbon nanotube (SWNT) by comparison with the structure restricted in a cylindrical mesopore of multi-wall carbon nanotube (MWNT) and that of bulk aqueous solution. The average micropore width of open-pore SWNT was 0.87 nm which is equivalent to the size of a hydrated zinc ion having 6-hydrated water molecules.

Pore size dependent behavior of hydrated Ag+ ions confined in mesoporous MCM-41 materials under synchrotron X-ray irradiation.

The behavior of hydrated Ag+ ions in a 1.5 mol dm(-3) AgNO3 aqueous solution confined in mesoporous silica MCM-41 with different pore sizes was characterized by synchrotron X-ray absorption spectroscopy. The hydrated Ag+ ions are stabilized in 4-fold coordination down to 195 K in the pores (21 Å in diameter), whereas in the larger pores (28 Å) the hydrated Ag+ ions are reduced to Ag0 to form nano clusters with the Ag-Ag interactions of 2.

High physisorption affinity of water molecules to the hydroxylated aluminum oxide (001) surface.

The adsorption mechanism of water on the hydroxylated (001) plane of α-Al(2)O(3) was studied by measuring adsorption isotherms and GCMC simulations. The experimental adsorption isotherms for three α-Al(2)O(3) samples from different sources are typical type II, in which adsorption starts sharply at low pressures, suggesting a high affinity of water to the Al(2)O(3) surface. Water molecules are adsorbed in two registered forms (bilayer structure).

Visible-light-derived photocatalyst based on TiO(2-δ)Nδ with a tubular structure.

We succeeded in achieving visible-light responsiveness on a tubular TiO(2) sample through the treatment of a tubular TiO(2) that has a large surface area with an aqueous solution of ammonia or triethylamine at room temperature and subsequent calcination at 623 K, which produced a nitrided tubular TiO(2) sample. It was found that the ease of nitridation is dependent on the surface states; washing the tubular TiO(2) sample with an aqueous acidic solution is very effective and indispensable. This treatment causes the appearance of acidic sites on the tubular TiO(2), which was proved by the following experiments: NH(3) temperature-programmed desorption and two types of organic reactions exploiting the acid properties.

Mechanism of freezing of water in contact with mesoporous silicas MCM-41, SBA-15 and SBA-16: role of boundary water of pore outlets in freezing.

The freezing mechanism of water contacted with mesoporous silicas with uniform pore shapes, both cylindrical and cagelike, was studied by thermodynamic and structural analyses with differential scanning calorimetry (DSC) and X-ray diffraction (XRD) together with adsorption measurements. In the DSC data extra exothermic peaks were found at around 230 K for water confined in SBA-15, in addition to that due to the freezing of pore water. These peaks are most likely to be ascribed to the freezing of water present over the micropore and/or mesopore outlets of coronas in SBA-15.

Thermodynamic and FTIR studies of supercooled water confined to exterior and interior of mesoporous MCM-41.

The thermal properties of water confined to both exterior and interior of cylindrical mesoporous MCM-41 (pore diameter d = 1.8-3.6 nm) were analysed by differential scanning calorimetry and FTIR spectroscopy.

Effect of water on structure of hydrophilic imidazolium-based ionic liquid.

The state of water in room-temperature ionic liquid, 1-ethyl-3-methylimidazolium tetrafluoroborate (EMI(+)BF(4)(-)), has been investigated by measurements of absorption and desorption isotherms, attenuated total reflectance infrared (ATR-IR) spectroscopy, and (2)H NMR relaxation method. The absorption enthalpies of water for the ionic liquid were estimated from the absorption isotherms. The enthalpies in the water mole fraction range of x(w) View Article and Find Full Text PDF

Effect of confinement on the fluid properties of ammonia in mesopores of MCM-41 and SBA-15.

The effect of pore size on capillary condensation and solid-liquid phase changes of ammonia in MCM-41 and SBA-15 was studied by adsorption and FTIR measurements of condensed phases at low temperatures. Adsorption isotherms are all typical type IV on the fully hydroxylated surfaces, without hysteresis loops in the smaller pores (d < 2.4 nm).

Aggregation of imidazolium ionic liquids in molecular liquids studied by small-angle neutron scattering and NMR.

The aggregation of two imidazolium-based ionic liquids, 1-ethly-3-methylimidazolium chloride (EMI(+)Cl(-)) and EMI(+) bis-(trifluoromethanesulfonyl)amide (EMI(+)TFSA(-)), in molecular liquids, water, methanol, acetonitrile, and benzene, has been studied by using the small-angle neutron scattering (SANS) technique. The SANS results have shown that the heterogeneity of EMI(+)Cl(-)-acetonitrile mixtures is significant at high acetonitrile contents, thus, EMI(+)Cl(-) forms clusters in acetonitrile solutions. On the other hand, it has been revealed that EMI(+)Cl(-) is homogeneously dissolved in water and methanol.

Thermodynamic, structural, and dynamic properties of supercooled water confined in mesoporous MCM-41 studied with calorimetric, neutron diffraction, and neutron spin echo measurements.

Thermodynamic, structural, and dynamic properties of heavy water (D(2)O) confined in mesoporous silica glass MCM-41 C10, C12, and C14 were investigated by differential scanning calorimetry, neutron diffraction, and neutron spin echo (NSE) measurements, respectively. The DSC data showed that no crystallization of D(2)O confined in C10 occurs in a temperature range between 298 and 180 K, and that crystalline ice is formed at 204 and 221 K for C12 and C14, respectively. For C10, the neutron radial distribution functions of confined D(2)O suggested a structural change in the supercooled state between 223 and 173 K.

Investigating hydration dependence of dynamics of confined water: monolayer, hydration water and Maxwell-Wagner processes.

The dynamics of water confined in silica matrices MCM-41 C10 and C18, with pore diameter of 21 and 36 A, respectively, is examined by broadband dielectric spectroscopy (10(-2)-10(9) Hz) and differential scanning calorimetry for a wide temperature interval (110-340 K). The dynamics from capillary condensed hydration water and surface monolayer of water are separated in the analysis. Contrary to previous reports, the rotational dynamics are shown to be virtually independent on the hydration level and pore size.

Interlayer water molecules in vanadium pentoxide hydrate. IX. Anisotropic translational diffusion leading to anisotropic ac conductivity.

The anisotropy of the dynamic properties of interlayer water molecules along the a and b axes of vanadium pentoxide hydrate, orthorhombic V2O5.nH2O, was studied using quasielastic neutron scattering (QENS) in relation to the anisotropy of the ac conductivity. The QENS spectra were analyzed using a stretched exponential function and a Lorentzian function.

Phase separation of acetonitrile-water mixtures and minimizing of ice crystallites from there in confinement of MCM-41.

The effect of confinement of an acetonitrile-water mixture, whose correlation length was comparable to the pore size of the mesopores of MCM-41 (d=2.4-3.6 nm), on the phase changes was studied.

Enthalpy and interfacial free energy changes of water capillary condensed in mesoporous silica, MCM-41 and SBA-15.

The effect of confinement on the solid-liquid phase transitions of water was studied by using DSC and FT-IR measurements. Enthalpy changes upon melting of frozen water in MCM-41 and SBA-15 were determined as a function of pore size and found to decrease with decreasing pore size. The melting point also decreased almost monotonically with a decrease in pore size.

Structure of methanol confined in MCM-41 investigated by large-angle X-ray scattering technique.

Large-angle X-ray scattering (LAXS) measurements over a temperature range from 223 to 298 K have been made on methanol confined in mesoporous silica MCM-41 with two different pore diameters, 28 A (C14) and 21 A (C10), under both monolayer and capillary-condensed adsorption conditions. To compare the structure of methanol in the MCM-41 pores with that of bulk methanol, X-ray scattering intensities for bulk methanol in the same temperature range have also been measured. The radial distribution functions (RDFs) for the monolayer methanol samples showed that methanol molecules are strongly hydrogen bonded to the silanol groups on the MCM-41 surface, resulting in no significant change in the structure of adsorbed methanol with respect to the pore size and temperature.

Neutron scattering study on dynamics of water molecules in MCM-41. 2. Determination of translational diffusion coefficient.

Quasielastic neutron scattering (QENS) spectra of water-filled MCM-41 samples (pore diameters: 21.4 and 28.4 Angstrom) were measured over the temperature range 238-298 K and the momentum transfer range 0.

Low temperature properties of acetonitrile confined in MCM-41.

The effect of confinement on the phase changes and dynamics of acetonitrile in mesoporous MCM-41 was studied by use of adsorption, FT-IR, DSC, and quasi-elastic neutron scattering (QENS) measurements. Acetonitrile molecules in a monolayer interact strongly with surface hydroxyls to be registered and perturb the triple bond in the C[triple bond]N group. Adsorbed molecules above the monolayer through to the central part of the cylindrical pores are capillary condensed molecules (cc-acetonitrile), but they do not show the hysteresis loop in adsorption-desorption isotherms, i.

Preparation of visible-light-responsive TiO2-xNx photocatalyst by a sol-gel method: analysis of the active center on TiO2 that reacts with NH3.

Active reaction centers for ammonia on titanium oxyhydroxide were explored to direct the search for an efficient sol-gel method for the synthesis of a titanium oxynitride (TiO2-xNx) sample with an efficient responsiveness to the visible light constituting a main part of the solar spectrum. The results lead to the conclusion that the site giving IR bands at around 2195 cm(-1) for the adsorbed CO molecules at 300 K is a reactive site and behaves as Lewis acid site in the coordination environment of distorted five-coordinate Ti4+ ions. Ammonia molecules are adsorbed on such a site to form -NH2 and -OH species during the heat treatments at a temperature above 373 K, and they are ultimately incorporated into the TiO2 lattice as nitride through the dehydration at higher temperatures of up to 723 K, resulting in the formation of an anatase type of TiO2-xNx.

Interlayer water molecules in vanadium pentoxide hydrate. 8. Dynamic properties by quasi-elastic neutron scattering.

The dynamics of water molecules in the layered vanadium pentoxide hydrate, V(2)O(5).nH(2)O, were studied by quasi-elastic neutron scattering (QENS) measurements. Heterogeneity of the dynamic properties was confirmed by alpha-relaxation model analysis.