Graphene oxide-silica nanohybrids as fillers for PA6 based nanocomposites
- 1. Department of Civil, Environmental, Aerospace, Materials Engineering, University of Palermo, Viale delle Scienze, Ed. 6, 90128, Palermo, Italy and STEBICEF, Section of Biology and Chemistry, University of Palermo, Viale delle Scienze, Parco d'Orleans (Italy)
- 2. Dipartimento di Ingegneria Chimica, Gestionale, Informatica, Meccanica, University of Palermo, Viale delle Scienze, Ed. 6, 90128, Palermo (Italy)
- 3. Department of Civil, Environmental, Aerospace, Materials Engineering, University of Palermo, Viale delle Scienze, Ed. 6, 90128, Palermo (Italy)
- 4. STEBICEF, Section of Biology and Chemistry, University of Palermo, Viale delle Scienze, Parco d'Orleans II, 90128 Palermo (Italy)
Description
Graphene oxide (GO) was prepared by oxidation of graphite flakes by a mixture of H2SO4/H3PO4 and KMnO4 based on Marcano's method. Two different masterbatches containing GO (33.3%) and polyamide-6 (PA6) (66.7%) were prepared both via solvent casting in formic acid and by melt mixing in a mini-extruder (Haake). The two masterbatches were then used to prepare PA6-based nanocomposites with a content of 2% in GO. For comparison, a nanocomposite by direct mixing of PA6 and GO (2%) and PA6/graphite nanocomposites were prepared, too. The oxidation of graphite into GO was assessed by X-ray diffraction (XRD), Micro-Raman spectroscopy, scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) analyses. All these techniques demonstrated the effectiveness of the graphite modification, since the results put into evidence that, after the acid treatment, interlayer distance, oxygen content and defects increased. SEM micrographs carried out on the nanocomposites, showed GO layers totally surrounded by polyamide-6, this feature is likely due to the strong interaction between the hydrophilic moieties located both on GO and on PA6. On the contrary, no interactions were observed when graphite was used as filler. Mechanical characterization, carried out by tensile and dynamic-mechanical tests, marked an improvement of the mechanical properties observed. Photoluminescence and EPR measurements were carried out onto nanoparticles and nanocomposites to study the nature of the interactions and to assess the possibility to use this class of materials as semiconductors or optical sensors
Additional details
Identifiers
- DOI
- 10.1063/1.4876872;
Publishing Information
- Journal Title
- AIP Conference Proceedings
- Journal Volume
- 1599
- Journal Issue
- 1
- Journal Page Range
- p. 438-441
- ISSN
- 0094-243X
- CODEN
- APCPCS
Conference
- Title
- 7. international conference on times of polymers (TOP) and composites
- Dates
- 22-26 Jun 2014
- Place
- Ischia (Italy)
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 45101711
- Subject category
- S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Resource subtype / Literary indicator
- Conference
- Descriptors DEI
- COMPOSITE MATERIALS; ELECTRON SPIN RESONANCE; FILLERS; FORMIC ACID; GRAPHENE; GRAPHITE; MECHANICAL PROPERTIES; MECHANICAL TESTS; NANOSTRUCTURES; OXIDATION; OXIDES; PHOSPHORIC ACID; PHOTOLUMINESCENCE; POLYAMIDES; RAMAN SPECTROSCOPY; SCANNING ELECTRON MICROSCOPY; SILICA; X-RAY DIFFRACTION; X-RAY PHOTOELECTRON SPECTROSCOPY
- Descriptors DEC
- CARBON; CARBOXYLIC ACIDS; CHALCOGENIDES; CHEMICAL REACTIONS; COHERENT SCATTERING; DIFFRACTION; ELECTRON MICROSCOPY; ELECTRON SPECTROSCOPY; ELEMENTS; EMISSION; HYDROGEN COMPOUNDS; INORGANIC ACIDS; INORGANIC COMPOUNDS; LASER SPECTROSCOPY; LUMINESCENCE; MAGNETIC RESONANCE; MATERIALS; MATERIALS TESTING; MICROSCOPY; MINERALS; MONOCARBOXYLIC ACIDS; NONMETALS; ORGANIC ACIDS; ORGANIC COMPOUNDS; ORGANIC POLYMERS; OXIDE MINERALS; OXYGEN COMPOUNDS; PHOSPHORUS COMPOUNDS; PHOTOELECTRON SPECTROSCOPY; PHOTON EMISSION; POLYMERS; RESONANCE; SCATTERING; SPECTROSCOPY; TESTING
Optional Information
- Notes
- (c) 2014 AIP Publishing LLC