Hybrid Surface (hybrid + surface)

Distribution by Scientific Domains


Selected Abstracts


Preparation and properties of organic,inorganic hybrid composites based on polystyrene and an incompletely condensed polyvinylsilsesquioxane oligomer

JOURNAL OF APPLIED POLYMER SCIENCE, Issue 5 2010
Zhen Dai
Abstract An incompletely condensed polyvinylsilsesquioxane (PVSQ) oligomer containing abundant silanol groups was synthesized and characterized by FTIR, 1H-NMR, 29Si-NMR, and MALDI-TOF-MS. Polystyrene/polyvinylsilsesquioxane (PS/PVSQ) hybrid composites were prepared by an in situ bulk polymerization. The hybrid composites showed higher Tg, Td, and char yield than PS homopolymer and without mechanical loss. The improvements in the properties of PS/PVSQ hybrid composites can be ascribed to the crosslinking function of PVSQ by silanol condensation in later processing. The hybrids showed different morphology from discrete microstructure to continuous network depending on the concentration of PVSQ. Because of the surface enrichment, a PVSQ protection layer was formed, which made the hybrid surface more hydrophobic. The structure and the reaction mechanism of PS/PVSQ hybrid composites were also investigated. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 [source]


Spontaneous segregation on a hybrid chiral surface

JOURNAL OF COMPUTATIONAL CHEMISTRY, Issue 10 2008
Szabelski
Abstract Segregation of enantiomers in two-dimensional adsorbed layers is a process that is usually controlled by anisotropic directional interactions between adsorbed molecules. In this contribution, we propose a simple theoretical model in which the chiral segregation occurs even though the lateral interactions are neglected. In particular, we consider a solid surface composed of two domains with different patterns of active sites being mirror images of each other. The domains of opposite handedness represent crystal facets of a composite chiral material which are adjoined to form a heterochiral adsorbing surface. To explore equilibrium properties of the system, we use Canonical Ensemble Monte Carlo method for a square lattice. The influence of factors such as energetic properties of the surface and density of the adsorbed layer on the extent of separation is examined. The obtained results indicate that effective two-dimensional separation on the hybrid chiral surface assumed in our model can be achieved only at sufficiently low adsorbate densities. The results also suggest that the segregation on the hybrid surface would be a promising method of enantiodiscrimination for those chiral molecules which do not exhibit strong lateral interactions. © 2008 Wiley Periodicals, Inc. J Comput Chem 2008 [source]


Reversibly Light-Switchable Wettability of Hybrid Organic/Inorganic Surfaces With Dual Micro-/Nanoscale Roughness

ADVANCED FUNCTIONAL MATERIALS, Issue 8 2009
Gianvito Caputo
Abstract Here, an approach to realize "smart" solid substrates that can convert their wetting behavior between extreme states under selective light irradiation conditions is described. Hybrid organic/inorganic surfaces are engineered by exploiting photolithographically tailored SU-8 polymer patterns as templates for accommodating closely packed arrays of colloidal anatase TiO2 nanorods, which are able to respond to UV light by reversibly changing their surface chemistry. The TiO2 -covered SU-8 substrates are characterized by a dual micro-/nanoscale roughness, arising from the overlapping of surfactant-capped inorganic nanorods onto micrometer-sized polymer pillars. Such combined architectural and chemical surface design enables the achievement of UV-driven reversible transitions from a highly hydrophobic to a highly hydrophilic condition, with excursions in water contact angle values larger than 100°. The influence of the geometric and compositional parameters of the hybrid surfaces on their wettability behavior is examined and discussed within the frame of the available theoretical models. [source]


Monitoring the synthesis of new polymer nanocomposites based on different polyhedral oligomeric silsesquioxanes using Raman spectroscopy

JOURNAL OF RAMAN SPECTROSCOPY, Issue 11 2009
Nicoleta Mihaela Sulca
Abstract The kinetic behavior of the urethane dimethacrylate (UDMA) copolymerized and reinforced by different concentrations of polyhedral oligomeric silsesquioxane (POSS) with methacrylic groups was studied through Raman spectroscopy. UDMA-POSS networks have been synthesized with three different types of POSS, two monofunctional POSS (1-propylmethacrylate)-heptaisobutyl substituted (HISO-POSS) and heptacyclopentyl-octasiloxan-1-yloxy) dimethylsilyl] propyl methacrylate (CPENTYL-POSS) and one octafunctional POSS-methacryl substituted (MA-POSS). In order to show the influence of POSS on the final conversion, the hybrid systems were cured using three types of initiators which decompose at different temperatures: azobisisobutyronitrile (AIBN) (65 °C), benzoyl peroxide (BP) (80 °C) and di- tert -butyl peroxide (DTBP) (120 °C). The structure of the hybrid's surface was investigated by X-ray photoelectron spectroscopy (XPS) and the Tg values were calculated from dynamic mechanical analysis (DMA) tests. Copyright © 2009 John Wiley & Sons, Ltd. [source]