The formation of mesophase silica-surfactant thin films at the air/solution interface has been studied in situ using off-specular X-ray reflectivity, Brewster angle microscopy and small angle scattering. Results for cetyltrimethylammonium bromide-templated films suggest that the formation mechanism is strongly dependent on the silica:surfactant ratio, and this is confirmed by studies on the subpha

Carbon nanoparticles with phenylsulfonate negative surface functionality (Emperor 2000, Cabot Corp.) are coated with positive chitosan followed by hydrothermal carbonization to give highly pH-responsive core-shell nanocarbon composite materials. With optimised core-shell ratio (resulting in an average shell thickness of ca. 4 nm, estimated from SANS data) modified electrodes exhibit highly pH-sens

Nanotechnology is the science of making and using very small structures. As the scales of the constructions become smaller, the existing methods of making these structures - lithography, etching and micromoulding - although constantly improving, will reach physical limits. To overcome the limitations and create smaller, designed and ordered structures, a so-called 'bottom-up' approach must be used

The preparation of chemisorbents based on tungsto- and molybdophosphoric acids supported on two types of synthetic mesoporous carbons and two types of mesoporous silica is described. Strong solid acids with good accessibility to acid sites may potentially be effective adsorbents for the removal of basic molecular impurities, such as amines, from ultrapure manufacturing environments. Prepared mater

We study the electrochemical roughening of a silicon electrode surface during the hydrogen evolution reaction in a fluoride electrolyte using neutron reflection. We demonstrate that as the roughening process modifies the morphology of the silicon surface we can follow the changes by observing the changes in the shape of the total reflection feature. We assume that the change in the morphology of t

Neutron reflectometry has been used to study the development of mesoporous silicated films at a hydrophilic silicon-solution interface. We find the time for film formation was altered in a manner similar to that seen at the air-liquid interface as the silica source-to-surfactant ratio was altered. Interestingly for films grown at the silica-liquid interface in a cell with no air space only one gro

A thin composite film of carbon nanoparticles (ca. 8 nm diameter) and chitosan biopolymer (poly-D-glucosamine, from chitin, 75-85% deacetylated) was prepared by evaporation from aqueous dispersion onto glassy carbon electrode surfaces. The amine groups in the chitosan biopolymer were used to effectively bind Hg(II) ions from an aqueous pH 5 KCl solution. During redox cycling voltammetric responses

The use of a semi-empirical alternative to the standard Washburn equation for the interpretation of raw mercury porosimetry data has been advocated. The alternative expression takes account of variations in both mercury contact angle and surface tension with pore size, for both advancing and retreating mercury meniscii. The semi-empirical equation presented was ultimately derived from electron mic

In situ characterisation of a growing surfactant-templated silica film has been carried out by X-ray reflectivity, diffuse X-ray scattering from the surface. Brewster angle microscopy and surface pressure measurements. The results indicate an unexpected film growth mechanism where layered structures form in solution and diffuse to the interface after some critical induction period.

A facile in situ nanoparticle seeding method is reported to prepare MIL-101(Cr) films on alumina supports. The in situ seeding of MIL-101(Cr) nanoparticles was promoted by use of dimethylacetamide (DMA). The generality of this approach is further demonstrated for Cu3(btc)2 films by using a (poly)acrylate promoter.

Off-specular X-ray reflectivity measurements were carried out to follow the in situ development of surfactant-templated silica thin films at the air-water interface under conditions of controlled relative humidity and temperature, using an enclosed sample cell designed for this purpose. The results suggest a strong dependence of formation time and growth mechanism on ambient conditions. Thin films

Colloidal ZnO is obtained during microwave-enhanced electrochemical deposition experiments from an aqueous solution containing 0.1 M Zn(NO 3)2 and 0.02 M H2O2 via repetitive negative going potential cycles from 0.3 to -0.8 V vs. SCE. The effects of temperature and temperature gradients on ZnO electro-formation at fluorine doped tin oxide (FTO) electrodes are investigated with both a conventional t

We have investigated the spontaneous self-assembly of solid, mesostructured films that form at the air-solution interface on solutions containing a neutral water-soluble polymer and catanionic surfactant mixtures of hexadecyl-trimethylammonium bromide (CTAB) and sodium dodecylsulphate (SDS). The formation processes and structures were probed using neutron reflectivity, X-ray reflectivity, off-spec

Micron-thick hydrogel films with ordered 3D mesostructures form spontaneously at the interface of polyelectrolyte-surfactant solutions. Here we demonstrate that by rationally designing the micelle shapes it is possible to predict and so tailor the nanostructure formed within surfactant-polyelectrolyte films. Using quaternary ammonium surfactants with a range of packing parameters, we demonstrate t

The mechanisms of entrapment, and the nanoscopic spatial distribution, of the residual mercury within nano-cast and amorphous porous media (pore sizes ∼1-100 nm) following high-pressure penetration have been studied. It has been shown that, even at the nanoscale, one of the same two principle mechanisms that have been observed previously in mercury porosimetry experiments on macroscopic glass pore

Highly structured catalyst support pellets have been produced that possess multiple, but regiospecific and well-defined, pore geometries. Mesoporous silica pellets with controlled pore sizes have been synthesised using one type of pore template for the pellet core zone, whilst using a different type of template for the surrounding shell region. These materials offer the potential of adding precise

Chemically surface-modified (tosyl-functionalized) carbon nanoparticles (Emperor 2000 from Cabot Corp.) are employed for the extraction and electrochemical determination of phenolic impurities such as benzophenone-3 (2-hydroxy-4-methoxybenzophenone) or triclosan (5-chloro-2-(2,4-dichlorophenoxy)phenol). The hydrophilic carbon nanoparticles are readily suspended and separated by centrifugation prio

The synthesis of surfactant-templated silicate materials has developed rapidly over the past decade. The uniform controlled pore sizes created in the amorphous silicate framework by this method show promise as catalyst supports, sensors, filtration membranes and in a variety of optoelectronic applications. Formation of these materials in a thin-film or membrane geometry is therefore an active area

Orientational ordering under shear was observed for some precursor gels for the synthesis of the hexagonal mesoporous silica MCM-41 in the presence of high KBr concentrations. The presence of KBr disrupted the formation of the first-order MCM-41 diffraction peak dependent upon KBr concentration. Synthesis gels which formed good quality MCM-41, but with no added KBr salt, were not oriented by stron

Adsorption isotherms taken at temperatures ranging from 20 to 77 K show a large pore volume and surface area of 980 m2 g-1 for the physical adsorption of molecular hydrogen on MCM-41. The adsorbed hydrogen behaves more like a solid than a liquid and isosteric heats of adsorption reveal a heterogenous surface. The evaporation behaviour of the adsorbed hydrogen indicates that the hexagonally packed