Search results for "X-Ray scattering"
showing 10 items of 165 documents
Fine-Tuning of the film thickness of ultrathin multilayer films composed of consecutively alternating layers of anionic and cationic polyelectrolytes
2007
We have recently introduced a new method of creating ultrathin films [1–3] based on the electrostatic attraction between opposite charges. Consecutively, alternating adsorption of anionic and cationic polyelectrolytes leads to the formation of multilayer assemblies. Multilayer buildup is easily monitored by small angle x-ray scattering (SAXS). The total thickness of the multilayer assemblies increases linearly with the number of adsorbed layers, indicating a stepwise and regular deposition process. — Here, we report on the fine-tuning of the total film thickness by changing the ionic strength of the solvent from which the polyelectrolytes are adsorbed. When the anionic polyelectrolyte is ad…
Dilute and semi dilute solutions of block copolymers in water, near-critical and super-critical CO2: a small angle scattering study of the monomer–ag…
2002
Abstract Small angle neutron (SANS) and X-ray (SAXS) Scattering measurements on aggregate formation of block copolymers in water and in near-critical and supercritical CO2 are reported here. Time Resolved SAXS (TR-SAXS) has also been performed in the supercritical region. Experiments have been carried out for a series of different thermodynamic conditions, changing the solvent density by profiling the pressure at constant temperature. A sharp transition between monomers dissolved as random coils and micelles characterized by a solvo-philic shell and a solvo-phobic core occurs when the solvent density reaches the critical micellization value. This is easily shown in the case of scCO2.
Combined SANS and SAXS experiments in polyolefins-hydrogenated oligocyclopentadiene (HOCP) blends
1998
Abstract Lamellar morphology in semicrystyalline polymer blends (iPP/HOCP and HDPE/HOCP) is investigated by means of Small Angle X-ray Scattering (SAXS) and Small Angle Neutron Scattering (SANS). The investigated blends present a complex phase diagram, as they show a miscibility gap. SAXS scattering curves of blends lying outside the miscibility gap can be analysed in the frame of the psuedo two phase model. In order to describe the complex morphology of blends lying inside the miscibility gap, the SANS technique revealed necessary. In this paper a novel method to describe the morphology of these complex systems by means of SANS is presented.
Self-assembly in surfactant-based mixtures driven by acid–base reactions: bis(2-ethylhexyl) phosphoric acid–n-octylamine systems
2013
Structural and dynamic features of bis(2-ethylhexyl) phosphoric acid (HDEHP)-n-octylamine (NOA) mixtures as a function of the NOA mole fraction (X-NOA) have been investigated by SAXS, WAXS, IR, dielectric spectroscopy and polarized optical microscopy. In the 0 <= X-NOA < 0.5 range, mixtures are transparent liquids, while the abrupt formation of a waxy solid characterized by an hexagonal bidimensional structure occurs at X-NOA = 0.5. Such a composition-induced phase transition results from the synergetic effect of the progressive increase in number density of ordered HDEHP-NOA nanodomains with X-NOA. Mainly driven by an HDEHP to NOA proton transfer, the increase of structural order with X-NO…
Structural and morphological rearrangements in quenched poly(ethylene) by simultaneous SAXS/WAXS
2000
Structure formation by crystallization from the melt in a wide range of cooling rates (0.08-1 000°C/s) in low-density polyethylene has been studied by simultaneous small- and wide-angle X-ray scattering at the synchroton radiation source of DESY. The occurrence of two periodicities, characterized by different angular position of Bragg's maxima, was observed, pointing to the existence of two types of lamellar stacks, associated with two different long period values L 1 and L 2 (L 1 > L 2 ). L 1 depends on the cooling rate, whereas L 2 is almost constant. A comparison with isotactic polypropylene is performed, where a similar phenomenon takes place. While in the case of i-PP a definite correl…
A combined small-angle neutron and X-ray scattering study of block copolymers micellisation in supercritical carbon dioxide
2003
Small angle neutron and X-ray scattering (SANS and SAXS) are used to investigate the monomer–aggregate transition of fluorocarbon–hydrocarbon diblock copolymers in supercritical carbon dioxide. SANS data are analyzed using a polydisperse sphere core–shell model. Synchrotron SAXS data have been collected by profiling the pressure at different temperatures, and critical micellization densities have been obtained for a series of diblock solutions. Finally pressure jump experiments, combined with synchrotron SAXS, have revealed two steps in the dynamics of the formation of the aggregates.
Kinetics of block-copolymer aggregation in super critical CO2
2002
Small angle X-ray and neutron scattering (SAXS and SANS) are used to obtain structural information on the aggregation behavior of block-copolymers dissolved in supercritical CO2. The SANS technique is used to provide a detailed structural model for the micellar aggregates, which form below the critical micellization density (CMD), that we defined in our previous work. The SAXS technique (with a synchrotron source) is used to provide the first experimental information concerning the kinetic features of both formation and decomposition of such aggregates as soon as pressure jumps are applied to the solutions across the CMD. 2002 Elsevier Science B.V. All rights reserved.
CONTRIBUTION OF PSEUDO-FOCUSED SOFT PROTONS TO THE BACKGROUND OF ATHENA
2021
This PhD thesis explores the role of low energy protons, the so-called ‘soft protons', as a component of the background in view of the future ESA's X-ray mission Athena. As a matter of fact, a high level of soft proton flux at the focal plane of Athena can adversely affect the scientific goals of the mission. To prevent this, a correct estimate of the soft proton flux expected at the focal plane of the satellite is fundamental. Such an estimate can be achieved only if the reflectivity of soft protons from the optics is well understood, with efforts on both the experimental and the theoretical sides. To this aim, I applied the model of reflectivity of particles at grazing incidence proposed …
Physicochemical Investigation of Nanostructures in Liquid Phases: Ytterbium Nitrate Ionic Clusters Confined in Ytterbium Bis(2-ethylhexyl) Sulfosucci…
2007
The confinement of finite amounts of ytterbium nitrate in the nanoscopic space of ytterbium bis(2-ethylhexyl)sulfosuccinate (Yb(DEHSS) 3 ) reversed micelles dispersed in n-heptane has been investigated by UV-vis-NIR, FT-IR, and SAXS. The analysis of the experimental data is consistent with the hypothesis that Yb(NO 3 ) 3 is distributed among reversed micelles as small size ionic clusters surrounded by the Yb 3+ surfactant counterions and anionic heads while the surfactant alkyl chains point toward the solvent medium. As a consequence of confinement and interfacial effects, the ionic clusters display photophysical properties different from those in the bulk state or isolated species. Moreove…
Physicochemical Investigation of the Solubilization of Ytterbium Nitrate in AOT Reverse Micelles and Liquid Crystals
2006
A wide investigation of the solubilization of the water-soluble salt Yb(NO3)(3) in sodium bis(2-ethylhexyl)sulfosuccinate (AOT) reverse micelles and AOT liquid crystals has been carried out. After saturation of water/AOT/organic solvent w/o microemulsions with pure Yb(NO3)(3), the Yb(NO3)(3)/AOT composites were prepared by complete evaporation under vacuum of the volatile components (water and organic solvent) of the salt-containing microemulsions. It was observed that these composites can be totally dissolved in pure n-heptane or CCl4, allowing the solubilization of a noticeable amount of Yb(NO3)(3) in quite dry apolar media. By UV-vis-NIR, FT-IR, and H-1 NMR spectroscopies, some informati…