Na. Abdel-khalek et Ama. Omar, Relationship of structure to properties of some anionic surfactants as collectors in the flotation process. 2. Effect of phenyl group, J CHEM EN D, 44(1), 1999, pp. 138-141
Surface and thermodynamic properties of four synthetic anionic surfactants
are studied. The properties of these surfactants are correlated with their
flotation performance to upgrade a petroleum coke sample to minimize its im
purities. The surfactants are isomers for dodecylbenzenesulfonate of the sa
me molecular weight, but the benzene ring is attached to different carbon a
toms along the dodecyl chain. The results show that the position of benzene
ring, attached to the carbon chain, affects their surface and thermodynami
c properties. The values of critical micelle concentration (cmc), minimum a
rea per molecule (A(min)), effectiveness (Pi(cmc)) and efficiency (pC(20)),
to reduce surface tension of water, are decreased with changing the positi
on of benzene ring from carbon atom number 3 to 5. Increasing temperature i
s accompanied by an increase in each of cmc, minimum area per molecule (A(m
in)), Gibbs energy of micellization (Delta G(mic)(o)), and adsorption (Delt
a G(ad)(o)). Meanwhile, the values of surface tension (gamma(cmc)) at cmc,
surface excess concentration (Gamma(max)), and effectiveness (Pi(cmc)) to r
educe surface tension of water are decreased. There is a good relationship
between the structure of a surfactant and its efficiency as a collector. Ch
anging the position of the phenyl group along the alkyl chain of a surfacta
nt toward its central carbon atom (6 phi C12) improves its efficiency as a
collector.