Francesco Tampieri

A comparative electron paramagnetic resonance study of expanded graphites and graphene

Graphene, a novel electronic system with unprecedented characteristics, can be obtained using different methods, each producing materials with specific characteristics from the electronic point of view. Among these procedures, methods based on the expansion of graphite allow to obtain graphene material in rather high quantities. We have, then, conducted a comparative study of graphene materials produced by these methods by using electron paramagnetic resonance (EPR) techniques; single-layer commercial graphene produced using the Hummers method has been used as the reference. EPR techniques enable the study of some magnetic properties of different types of electrons exhibiting paramagnetic nature. We have analysed the EPR spectra to identify the different types of paramagnetic centres contributing to the spectrum. The analysis of the temperature-dependent EPR spectra and the use of pulse techniques allowed us to separate and characterize the contribution of free conduction electrons from the contributions of localized edge states and molecular-type paramagnetic states.

Online Quantification of Criegee Intermediates of α-Pinene Ozonolysis by Stabilization with Spin Traps and Proton-Transfer Reaction Mass Spectrometry Detection

Biogenic alkenes, which are among the most abundant volatile organic compounds in the atmosphere, are readily oxidized by ozone. Characterizing the reactivity and kinetics of the first-generation products of these reactions, carbonyl oxides (often named Criegee intermediates), is essential in defining the oxidation pathways of organic compounds in the atmosphere but is highly challenging due to the short lifetime of these zwitterions. Here, we report the development of a novel online method to quantify atmospherically relevant Criegee intermediates (CIs) in the gas phase by stabilization with spin traps and analysis with proton-transfer reaction mass spectrometry. Ozonolysis of α-pinene has been chosen as a proof-of-principle model system. To determine unambiguously the structure of the spin trap adducts with α-pinene CIs, the reaction was tested in solution, and reaction products were characterized with high-resolution mass spectrometry, electron paramagnetic resonance, and nuclear magnetic resonance spectroscopy. DFT calculations show that addition of the Criegee intermediate to the DMPO spin trap, leading to the formation of a six-membered ring adduct, occurs through a very favorable pathway and that the product is significantly more stable than the reactants, supporting the experimental characterization. A flow tube set up has been used to generate spin trap adducts with α-pinene CIs in the gas phase. We demonstrate that spin trap adducts with α-pinene CIs also form in the gas phase and that they are stable enough to be detected with online mass spectrometry. This new technique offers for the first time a method to characterize highly reactive and atmospherically relevant radical intermediates in situ.

Air non-thermal plasma treatment of Irgarol 1051 deposited on TiO2

The herbicide 2-(methylthio)-4-(tert-butylamino)-6-(cyclopropylamino)-s-triazine (tradename Irgarol 1051, abbreviated here as Irg), widely used in antifouling paints as biocide inhibiting seaweeds growth, is found in coastal waters in the vicinity of ports and harbors. In this work, Irg was subjected to air non-thermal plasma (NTP) treatment, alone and in the presence of TiO2. A dielectric barrier discharge reactor was used, powered by AC voltage (18 kV, 50 Hz) to produce air-NTP directly above the surface of the aqueous Irg solution to be treated. Due to the very fast degradation of Irg occurring under the experimental conditions used, the results of kinetic experiments failed to detect any rate enhancement due to titania induced photodegradation. We show, however, that pre-adsorption of Irg on titania provides a means to significantly increase Irg NTP-induced degradation throughput, a result which might have useful practical consequences. It is concluded that this phenomenon is due to the acidic character of TiO2 which brings more Irg in solution by increasing the value of the ionization ratio, [IrgH+]/[Irg]. Product analysis, performed by LC/ESI-MSn, allowed us to detect and identify numerous intermediates of Irg degradation and to propose different competing reaction pathways for the investigated NTP induced Irg advanced oxidation process. The extent of mineralization to CO2 was assessed by Total Carbon analysis. It was found to reach 95% after 5 h treatment of Irg solutions with an initial concentration of 5·10-6 M. These results confirm the capability of our NTP prototype reactor to mineralize persistent organic pollutants.