Search results for "OXIDATION"
showing 10 items of 1913 documents
Photo-oxidation behaviour of polyethylene/polyamide 6 blends filled with organomodified clay: Improvement of the photo-resistance through morphology …
2010
Abstract The impact of small amounts of organomodified clay (OMMT) on the photo-degradation behaviour of two blends obtained by mixing either low-density polyethylene (LDPE) or high density polyethylene (HDPE) with polyamide 6 (PA6) (LDPE/PA6 and HDPE/PA6 75/25 wt-%) was studied. The complex photo-degradation behaviour was followed by monitoring the main physical–mechanical properties of the blends. In particular, mechanical and spectroscopic tests were performed in conditions of accelerated artificial aging. An accurate mechanical and morphological characterization was previously carried out. The presence of the OMMT promotes the unexpected formation of a co-continuous morphology for the H…
Photocatalytic activity of binary and ternary SnO2–ZnO–ZnWO4 nanocomposites
2015
Binary and ternary SnO2-ZnO-ZnWO4 nanocomposites were prepared by a sol-gel route. The photocatalytic activity of the samples was evaluated through the decomposition of 4-nitrophenol and partial oxidation of 4-methoxybenzyl alcohol to p-anisaldehyde. All the mixed catalysts revealed higher photoactivity than bare ZnO, SnO2 or ZnWO4 and the best performances were exhibited by the binary nanocomposites. The high photocatalytic activity was explained by the presence of heterojunctions among different semiconductors that enhance the separation of the photogenerated electron-hole pairs, hindering their recombination. As a general consideration, an essential role was played by the electronic feat…
Low-density polyethylene/polyamide/clay blend nanocomposites: Effect of morphology of clay on their photooxidation resistance
2017
The photooxidation behaviour of low-density polyethylene (LDPE)/polyamide (PA) blends, containing polyamide 11 (PA11) or polyamide 6 (PA6), has been investigated in the absence and presence of a small amount of commercial organomodified clay (OMMT). The polymer blends LDPE/PA11 and LDPE/PA6 at 75/25 wt./wt.%, with and without OMMT, have been prepared by a two-step procedure: extrusion and sheet formulation. The formulated complex systems have been subjected to accurate morphological analysis in order to evaluate the effect of the OMMT presence on the refinement of the blend morphology. Furthermore, the produced sheets have been subjected to arterial UVB exposure and the variations of the me…
UV-stabilisation of polystyrene-based nanocomposites provided by polyhedral oligomeric silsesquioxanes (POSS)
2012
Abstract The photo-ageing behaviour of Polyhedral Oligomeric SilSequioxane (POSS)-polystyrene (PS) nanocomposites has been investigated for the first time. POSS having different inorganic framework and pendant organic groups have been used in the PS nanocomposite preparation and the formulated films were subjected to accelerated weathering. Compared to pristine PS, the POSS-containing PS developed a lower level of carbonyl and hydroxyl groups as a function of the exposure time, indicating a significantly improved resistance of the nanocomposites to photo-degradation. The results suggest that all of the investigated POSS molecules play a protective role and may extend the in-use lifetime of …
Shape-dependency activity of nanostructured CeO2 in the total oxidation of polycyclic aromatic hydrocarbons
2013
11 figures, 2 tables.-- © 2012. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/
Nanosponge-C3N4 composites as photocatalysts for selective partial alcohol oxidation in aqueous suspension
2023
A set of four composite materials was prepared, consisting of a nanosponge matrix based on beta-cyclodextrin in which carbon nitride was dispersed. The materials were characterized by the presence of diverse cross-linker units joining the cyclodextrin moieties, in order to vary the absorption/release abilities of the matrix. The composites were characterized and used as photocatalysts in aqueous medium under UV, visible and natural solar irradiation for the photodegradation of 4-nitrophenol, and for the selective partial oxidation of 5-hydroxymethylfurfural and veratryl alcohol to the corresponding aldehydes. The nanosponge-C3N4 composites showed higher activity than the pristine semiconduc…
Nanosponge-C3N4 composites with improved photocatalytic activity for selective partial alcohol oxidation in aqueous suspension
2022
Composites of C3N4 with nanosponges based on β-cyclodextrins containing a 5% w/w of C3N4 were synthesised, physicochemicaly characterised and tested as heterogeneous photocatalysts for the degradation of 4-nitrophenol and for the partial oxidation of 5-hydroxymethyl-2-furfural and veratryl alcohol. The results outline a synergistic effect in terms of conversion and selectivity. The association of the nanosponges with the C3N4 enhances the photocatalytic activity of the semiconductor, possibly due to the local concentration effect occurring on the photocatalyst surface that would involve a concentration into the nanosponge matrix ca. 500 times larger than in the solution bulk. Composites of …
Local photo-oxidation of individual single walled carbon nanotubes probed by femtosecond four wave mixing imaging
2014
Photo-oxidation of individual, air-suspended single walled carbon nanotubes (SWCNTs) is studied by femtosecond laser spectroscopy and imaging. Individual SWCNTs are imaged by four wave mixing (FWM) microscopy under an inert gas (Ar or N2) atmosphere. When imaging is performed in an ambient air atmosphere, the decay of the FWM signal takes place. Electron microscopy shows that SWCNTs are not destroyed and the process is attributed to photoinduced oxidation reactions which proceed via a non-linear excitation mechanism, when irradiation is performed with ∼30 fs pulses in the visible spectral region (500-600 nm). Photo-oxidation can be localized in specific regions of SWCNTs within optical reso…
Oxidative decarboxylation of naproxen.
1992
The decarboxylation of naproxen (1H) and its salt (1-) was achieved by means of chemical [Ce(IV) or S2O8(2-)] and electrochemical oxidation. The product patterns were compatible with mechanisms involving single-electron transfer from the pi-system or the carboxylate moiety. The results are discussed in connection with the involvement of electron-transfer processes in the reported phototoxicity of naproxen.