Ec. Butler et Kf. Hayes, MICELLAR SOLUBILIZATION OF NONAQUEOUS PHASE LIQUID CONTAMINANTS BY NONIONIC SURFACTANT MIXTURES - EFFECTS OF SORPTION, PARTITIONING AND MIXING, Water research, 32(5), 1998, pp. 1345-1354
Surfactant micellar solubilization is under investigation as a promisi
ng method for significantly increasing the efficiency of remediation o
f aquifers contaminated with nonaqueous phase liquids (NAPLs). In this
study, the influence of three parameters on the micellar solubilizati
on of NAPLs by a mixture of ethoxylated dodecyl alcohol surfactants wa
s investigated: Presence of model aquifer materials, extent of equilib
rium partitioning of surfactant into the nonaqueous phase, and sample
mixing regime. The micellar solubilization of two NAPLs, hexane, repre
sentative of nonbranched alkanes, and 1,2-dichlorobenzene, representat
ive of polar and aromatic compounds, was studied. Batch experiments in
dicated that surfactant losses to sorption on organic-coated silica we
re relatively small for these experimental systems. Surfactant partiti
oning into hexane was not significant, but there was significant surfa
ctant partitioning into the 1,2-DCB phase, resulting in a total surfac
tant dose required to achieve 1,2-DCB micellar solubilization greater
than that predicted from the surfactant critical micelle concentration
. Partitioning of surfactant into 1,2-DCB was selective, with the more
hydrophobic surfactant molecules Favoring the 1,2-DCB phase, resultin
g in an aqueous phase surfactant mixture with different solubilization
properties than the original. Mixing conditions had a significant eff
ect on the extent of solubilization of 1,2-DCB, attributed to the grea
ter tendency of 1,2-DCB versus hexane to form emulsions. Results indic
ate that partitioning may be significant for certain nonionic surfacta
nt/NAPL systems and should be investigated prior to remedial activitie
s. Total surfactant concentration, aqueous to nonaqueous phase volume
ratio, and surfactant formulation should be chosen to minimize losses
to nonaqueous phases. (C) 1998 Elsevier Science Ltd. All rights reserv
ed.