0000000000446951

AUTHOR

Roberto Milani

0000-0002-7997-7847

showing 3 related works from this author

Reactions Occurring during the Melt Mixing of Nylon 6 and Oxazoline−Cyclophosphazene Units

2009

Specific reactions of amino and carboxyl end groups of Nylon 6 with the reactive oxazoline groups belonging to a cyclophosphazene compound (referred as CP20XA) were carried out at 240 °C for different times, under inert atmosphere. Ny6 polymers terminated with one specific reactive chain end (-COOH or NH2) were reacted with different amounts of CP20XA to study the kinetic order of the reactions. All Ny6-CP20XA reacted products soluble in trifluoroethanol (TFE) were well characterized by MALDI-TOF MS, FT-IR and ( 1H and 13C) NMR techniques. The MALDI-TOF results show that the oxazoline rings react with the carboxyl chain ends of Ny6 following second-order kinetics. The reactions with amino c…

chemistry.chemical_classificationOxazolineReaction mechanismPolymers and PlasticsOrganic ChemistryKineticsSide reactionPolymerOxazolineReactive BlendingInorganic Chemistrychemistry.chemical_compoundEnd-groupSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiNylon6Nylon 6chemistrycyclophosphazenes polyamide end-functionalization MALDI-TOFMaterials ChemistryOrganic chemistryInert gasMALDIMacromolecules
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Surface modification of poly(ethylene-co-acrylic acid) with amino-functionalized silica nanoparticles

2011

In this work we studied the possibility to achieve a hybrid-surface through the modification, via a facile wet chemical process, of the surface of films of poly(ethylene-co-acrylic acid) (EAA) with amino-modified silica nanoparticles. Films of EAA were preliminarily activated by the introduction of -COCl groups on their surface. Silica nanoparticles were thereafter covalently bound on the polymeric surface as confirmed by FTIR, ATR-FTIR, XPS, NMR and SEM determinations. The nanoparticles formed a multilayer on the film surface and covered almost uniformly the whole film surface. Direct measurements of superficial amino groups by titration allowed us to detect a concentration of about 18 nmo…

nanostructured hybrid materialsMaterials scienceTRIALKOXYSILANE DERIVATIVESNanoparticleGeneral ChemistryCOATED MAGNETIC NANOPARTICLESContact anglechemistry.chemical_compoundSurface modificationchemistryChemical engineeringX-ray photoelectron spectroscopyPolymer chemistryMaterials Chemistrynanoparticles functionalizationSurface modificationWettingFourier transform infrared spectroscopyCOLLOIDAL SILICACATALYZED SYNTHESISAcrylic acidPolymeric surfaceJournal of Materials Chemistry
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Hierarchical Self-Assembly of Halogen-Bonded Block Copolymer Complexes into Upright Cylindrical Domains

2017

Summary Self-assembly of block copolymers into well-defined, ordered arrangements of chemically distinct domains is a reliable strategy for preparing tailored nanostructures. Microphase separation results from the system, minimizing repulsive interactions between dissimilar blocks and maximizing attractive interactions between similar blocks. Supramolecular methods have also achieved this separation by introducing small-molecule additives binding specifically to one block by noncovalent interactions. Here, we use halogen bonding as a supramolecular tool that directs the hierarchical self-assembly of low-molecular-weight perfluorinated molecules and diblock copolymers. Microphase separation …

Materials scienceBlock copolymerGeneral Chemical Engineering116 Chemical sciencesSupramolecular chemistryNanotechnologyblock copolymer02 engineering and technologyhierarchical self-assembly010402 general chemistry01 natural sciencesBiochemistryMicelleArticleSDG9: Industry innovation and infrastructuresupramolecular complexesMaterials ChemistryCopolymerEnvironmental ChemistryNon-covalent interactionsMoleculeLamellar structureta116chemistry.chemical_classificationHalogen bondta114Biochemistry (medical)General Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesblock copolymerschemistryChemical engineeringIndustry innovation and infrastructure [SDG9]nanofabricationhalogen bondSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelf-assembly0210 nano-technology
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