SPECTROSCOPIC INVESTIGATIONS IN MOLECULARLY ORGANIZED SOLVENT MEDIA -PART-3 - EXAMINATION OF THE NITROMETHANE SELECTIVE QUENCHING RULE IN AQUEOUS ANIONIC PLUS CATIONIC AND ANIONIC PLUS NONIONIC MIXED SURFACTANT SOLUTIONS
S. Pandey et al., SPECTROSCOPIC INVESTIGATIONS IN MOLECULARLY ORGANIZED SOLVENT MEDIA -PART-3 - EXAMINATION OF THE NITROMETHANE SELECTIVE QUENCHING RULE IN AQUEOUS ANIONIC PLUS CATIONIC AND ANIONIC PLUS NONIONIC MIXED SURFACTANT SOLUTIONS, Fresenius' journal of analytical chemistry, 360(6), 1998, pp. 669-674
Applicability of the nitromethane selective quenching rule for discrim
inating between alternant versus nonalternant polycyclic aromatic hydr
ocarbons (PAHs) is examined for 20 representative PAH solutes dissolve
d in micellar sodium dodecylsulfate (SDS) + cetyltrimethylammonium bro
mide (CTAB), SDS + dodecyltrimethylammonium bromide (DTAP), SDS + Brij
-35, and SDS + sodium octanoate (SO) mixed surfactant solvent media. E
xperimental results show that nitromethane quenched fluorescence of al
l 8 alternant PAHs studied in the four different solvent systems. Unex
pected quenching behavior was observed, however, in the case of nonalt
ernant PAHs. Nitromethane quenched fluorescence emission of nonalterna
nt PAHs dissolved in the SDS + SO solvent media, which is contrary to
the selective quenching rule. In the case of the mixed anionic + catio
nic surfactant solvent media, nitromethane quenching selectivity was r
estored at concentration ratios of approximately 4:1 (anionic:cationic
) or less.