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The optimum conditions have been determined for preparing substituted diphenylamines using the Chapman rearrangement. The rearrangement was best carried out in boiling tetraglyme. Phenyl N-phenylcinnamidate rearranged at a lower temperature than the corresponding benzimidate.

Die substituierten Phosphine (I) reagieren mit Brom‐acetophenon (II) bei 0, 34 und 48°C in Nitromethan zu den Phosphoniumbromiden (III).

Carbon nanotubes (CNTs) were tested as catalysts in the selective denitrification of 4-nitrophenol (4-NP) from oily wastewater by catalytic wet peroxide oxidation (CWPO). The CNTs were prepared by chemical vapor deposition, feeding sequentially ethylene (E) and/or acetonitrile (A) during different times until 20 min, resulting in samples E20, A20 and E10A10, the number denoting the time feeding of each precursor and the order of appearance of the letter indicating the order of each precursor. The synthesized CNTs were tested in the CWPO of 4-NP in aqueous solutions and in simulated oily wastewater (2,2,4-trimethylpentane and water) at 80 ºC, initial pH 3.5, C4-NP = 1 g L-1, CH2O2 = 3.56 g/L and Ccatalyst = 2.5 g L-1. The catalyst A20 promoted a faster decomposition of H2O2 and a lower degradation of 4-NP in the aqueous system, whereas the catalyst E20 displayed the opposite trend, since E20 was able to remove 99% of the pollutant and A20 only 69% after 8 h of reaction. E10A10 in biphasic L-L media presented the highest conversion of 4-NP after 24 h in the oily phase (51%), followed by A20 (38%) and then E20 (25%). This tendency may be ascribed to the formation of Pickering emulsions by E10A10. The amphiphilic carachteristic of this material ensures a closer contact between the liquid phases, allowing higher mass transfer.