OH radical oxidation of the sorbitylfurfural furanic ring to sugar derivatives induced by radiolysis in aerobic environment

Chemical radiolytic oxidation induced by OH addition on 1-(2-furan-2-yl-5-hydroxy-6-hydroxymethyl-[1,3]dioxan-4-yl)-ethan-1,2-diol (sorbitylfurfural, SF) leads, in the presence of controlled amounts of oxygen, to a permanent functional modification of the target molecule. The yield of conversion reaches 60% of the starting material. LC-MS analysis allowed the identification, as final products, of carboxylic acids, butenal and hydroxy-furan derivatives in which the sugar chain remains unbroken, while the furanic ring is attacked first by OH and then by oxygen, giving in succession an intra-/inter-molecular rearrangement of the allylperoxyl radicals thus formed. The proposed oxidation of the furanic ring envisages the peroxyl intermediates undergoing mono- and/or bi-molecular reactions; a reaction path has been outlined and is reported here. The presence of unsaturated bonds in the final products could provide a further site for radical scavenger activity. Therefore, the fast reaction with O₂ and the rearrangement of the produced peroxyl radicals to species, which are likely to be effective OH-capturers, reinforces the antioxidant ability of SF.     

HLDPE/organic functionalized SiO2 nanocomposites with improved thermal stability and mechanical properties

High-pressure low-density polyethylene (HLDPE)/organic functionalized SiO₂ nanocomposites were synthesized using melt-blending technique in a sigma internal mixer. The properties of the nanocomposites were studied using two different organic functional modifiers: diglycidyl ether of bisphenol-A (DGEBA) and triacetoxyvinylsilane. Reinforcing, thermal stability and toughening effects of organic functionalized nanosilica on the polymer matrix were found at loading of 2.5% nanosilica functionalized with 2.8% of DGEBA and silane coupling agent respectively. Organic functionalization on the nanosilica particle surface led to different microstructures when compared with that of the pure polymer. Organic functionalization on the nanosilica particle surface produced good interfacial adhesion and homogeneous dispersion in the polymer matrix, while the use of nanosilica resulted in aggregated silica particles in the polymer matrix. There was no significant improvement in thermal stability and mechanical properties when only nanosilica was added to the pure polymer. On the contrary, the addition of pretreated nanosilica with organic functional modifiers led to an increase of thermal stability from 313–363°C, elastic modulus and toughness from 0.12–0.18 GPa and 3.23–9.81 MJ/m³ respectively.     

Polymer Surface Functionalization Using Plasma,Ultraviolet and Synchrotron Radiation

Polyurethane (PU) and polystyrene (PS) films were functionalized by ultraviolet (UV) or selective synchrotron radiations (SR) in the presence of reactive gases. The UV-PU results were compared with lowpressure plasma treatments of the same films. Oxygen or acrylic acid vapours (AA) were used as reactive gases. X-ray photoelectron spectroscopy measurements of UV modified films in the presence of oxygen or AA matched the RF-plasma treatments results. It is shown that COO and C=O functional groups were incorporated at the polymer surface efficiently with both methodologies. In addition, near-edge X-ray absorption fine structure showed that a thin film of poly(acrylic acid) is formed over the PU and PS films during the UV irradiation in the presence of AA vapours. These results resemble previous AA low-power plasma treatments. PU and PS films were also selectively functionalized by SR using oxygen as reactive gas. Surface concentrations of COO and C=O functional groups were enhanced by C_1s → σ* _C–C excitation after irradiation and oxygen introduction. This efficient surface functionalization was clearly observed in PS films which do not have CO and COO groups in their molecular structure. Excitations involving transitions to π* orbital (π*_C=C, π*_C=O) led to much lower functionalization efficiency. The SR results can be explained by taking into account previous photon stimulated ion desorption studies of polymers. SR results may open new ways to functionalize polymer surfaces selectively and efficiently.     

Carbon nanotube-polymer nanocomposites: The role of interfaces

Research aimed at producing new nanocomposites with improved properties has dramatically increased in the last decade, especially on materials tailored at a nanometric level, such as fullerenes and carbon nanotubes. The use of nanoforms as reinforcement of organic polymers has opened the possibility of developing novel ultra-strong and conductive nanocomposites. Nevertheless, the challenge of manufacturing multifunctional composite materials based on nanostructures is still open, in particular in the details of the corresponding interfacial properties, which are particularly relevant in these systems. This paper reviews the main technical activities in this field, focusing on the most important parameters that influence the behavior of their interface, discussing recent advances, as well as current and future trends in research.     

Covalent attachment of polystyrene on multi-walled carbon nanotubes via nitroxide mediated polymerization

A new method to attach polymers on carbon nanotubes has been studied. We used nitroxide mediated polymerization (NMP) to graft polystyrene from multi-walled carbon nanotubes (MWNTs). Carboxyl groups on MWNTs were activated with thionyl chloride (SOCl₂) to give acyl chloride derivative (MWNT-COCl). NMP initiator was introduced to MWNT by esterification of 1-hydroxy-2-phenyl-2-(2′,2′, 6′, 6′-tetramethyl-1′-piperidinyloxy)ethane (HO-PE-TEMPO) with acyl chloride groups of MWNTs. The obtained MWNT-PE-TEMPO was used for initiation of bulk polymerization of styrene, yielding polystyrene-grafted MWNTs (MWNT-g-pSt). The resulting composites of MWNT-g-pSt were analyzed by TEM, SEM, FT-IR and TGA.     

Mechanical and Thermal Properties of Amine Functionalized Multi-walled Carbon Nanotubes Epoxy-Based Nanocomposite

This study is focused on fabrication and characterization of multi-walled carbon nanotubes (MWCNTs) reinforced epoxy composites to understand variation of mechanical and thermal properties. Samples were prepared by infusing both amine functionalized and non-functionalized MWCNT into commercially available EL-350 epoxy resin. Flexure, quasi-static compression and high strain rate (HSR) tests were performed with 0.1%, 0.2% and 0.3% of MWCNTs to observe variation in mechanical properties. The optimum loading was found at 0.2%. Nanocomposites with amine functionalized MWCNTs showed better properties compared to that with unmodified MWCNTs. Scanning electron microscopy (SEM) analysis was performed to confirm an improvement in dispersion with functionalization. Thermal properties were investigated by thermogravimetric analysis (TGA).     

Studies on HDPE functionalized by ultraviolet irradiation and interfacial interaction of HDPE/STC blend

Compared with ultraviolet irradiation in air, high density polyethylene (HDPE) could be very quickly functionalized by ultraviolet irradiation in ozone atmosphere, introducing oxygen-containing groups such as C=O and C-O onto the molecular chains of HDPE. After ultraviolet irradiation in ozone atmosphere, the molecular weight of HDPE decreased, its distribution became wider, the melt index (MI) increased, and the water contact angle decreased. After irradiating for a short time in ozone atmosphere, the interfacial interaction between the irradiated HDPE and sericite-tridymite-cristobalite (STC) particles is improved. The yield and notched impact strength of the HDPE/STC (60/40) blend with 10 min-irradiated HDPE are increased from 25.5 MPa and 61 J/m for the nonirradiated HDPE/STC (60/40) blend to 30.2 MPa and 360 J/m for the irradiated blend, respectively.     

Covalent attachment of poly(ethylene glycol) on multi-walled carbon nanotubes

A new 'graft-onto' method to attach poly(ethylene glycol) (PEG) onto multi-walled carbon nanotubes (MWNTs) has been developed. The method is based on the coupling reaction of radicals formed at the chain end of PEG onto the surface of MWNTs. The polymeric radicals are generated by atom (halogen) transfer reaction between chloroacetyl-terminated PEG and transition metal catalysts. The method allows direct covalent attachment of PEG to pristine MWNTs without pretreatment that could alter their original structure. The resulting PEG-grafted MWNTs showed improved dispersion stability in isopropanol and methanol.