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Graphene sheets were functionalized covalently with an appropriate linker as a novel vector for p-DNA delivery into mammalian cells. The transfected cancer cells produced green fluorescence as an indicator of successful gene delivery.

Pharmaceutical compounds are emerging contaminants that have been detected in surface water across the world. Because conventional wastewater treatment plants are not designed to treat such pollutants, new technologies are needed to degrade and oxidize such contaminants. The newly developed oxy-cracking process was utilized to treat the antidiabetic drug, metformin. The process, which involved partial oxidation of metformin in alkaline aqueous medium, proved to decompose the drug into small organic molecules, with minimum emission of CO2, therefore, increasing its biodegradability and removal from industrial treatment plants. The reaction gaseous products were probed by online gas chromatography. The liquid phase before and after oxy-cracking was analyzed for total carbon content by TOC and gas chromatography mass spectrometry. The products formed from the nitrogen-rich drug included ammonia, amines, amidines, and urea derivatives. A reaction mechanism for the oxy-cracking process is proposed. Because the hydroxyl radical (˙OH) is believed to play a central role in the oxy-cracking process, the mechanism is initiated by ˙OH attacks on metformin, followed by single decomposition or isomerization steps into stable products. The reactions were investigated using density functional theory calculations and validated using high quality 2nd order Moller–Plesset perturbation theory energy calculations.

In this study, the thermal oxidation of an asphaltene model molecule, Quinolin-65, was investigated using the density functional theory (DFT) and the second-order Moller–Plesset (MP2) perturbation theory. The reactions studied involved thermal decompositions as well as the interactions between the model molecule and singlet atomic (O1D) and molecular (O21Δ) oxygen. The theoretical study was performed under conditions similar to those of the uncatalyzed thermal oxidation of asphaltenes. A new reaction pathway for the loss of the olefin chain in Quinolin-65 via a 1,3-hydrogen shift mechanism was revealed. Thermogravimetric analysis of Quinolin-65 was also performed and the reaction products were probed by a mass spectrometer. Both the theoretical study and the thermogravimetric analysis concluded that the thermo-oxidative decomposition of Quinolin-65 is a complex multi-step reaction process, which involves different reaction pathways. The thermodynamic parameters obtained in this study showed that the reaction process should start with the loss of the olefin chain in the Quinolin-65 molecule, followed by the oxidation of the aromatic chain, to produce mainly, H2O, CO2, and SO2.