Journal of Industrial and Engineering Chemistry, Vol.3, No.1, 29-36, March, 1997
Investigation of Solubilization Behavior for m-Chlorophenol by Polymeric and Copolymeric Surfactants in the Aqueous Phase
Anionic polymeric and copolymeric surfactants were prepared respectively from 10- undecen-1-ylsulfate micelle and 10-undecenol as a polymerizable additive. The resulting polymeric and copolymeric surfactants were characterized using ¹H-NMR and a surface tensiometer. It has been confirmed that the copolymeric surfactant has 3 sulfate to 1 alcohol group repeat unit and that both polymeric and copolymeric surfactants can form micelles without critical micellar concentration (CMC). The solubilization of m-chlorophenol in aqueous solutions of the anionic polymeric and copolymeric surfactants at 25℃ has been studied using semiequilibrium dialysis. Complete solubilization isotherms have been determined for m-chlorophenol in the polymeric and copolymeric micelles below the CMC of 10-undecen-1-yl sulfate. The solubilization equilibrium (or partition) constant for the copolymeric micelle was slightly higher than that of the polymeric micelle. As usual, the solubilization equilibrium constant decreased with increasing mole fraction of m-chlorophenol in the micelles. Those results have been discussed based on a surface binding view point.
- Cooper WJ, Chemistry in Water Reuse, Chap. 12, 243-286, Ann Arbor, Michigan (1981)
- Robertson JH, Cowen WF, Longfield JY, Chem. Eng., 30, 102 (1980)
- Ember LR, Kirchner EM, Mileman B, Rawl RL, Lepkowski W, Chem. Eng. News, 30, 36 (1990)
- Christian SD, Scamehorn JF, In Surfactant-Based Separation Processes; J.F. Scamehorn, and J.H. Harwell (eds.), 7, Marcel Dekker, New York (1989)
- Dum RO, Scamehorn JF, Christian SD, Sep. Sci. Technol., 20, 257 (1985)
- Since the micelle is formed by the aggregation of about 80-150 monomeric surfactants, and in fast equilibrium state with it's monomers (micelle↔monomers), the monomeric surfactant can only form the micelle only under the presence of enough amount of monomeric surfactants in the solution, in other words, above CMC. This presence of CMC and be determined by various methods (in this paper, we used the surface tension measurement method). While all of the monomeric surfactants have their own characteristic CMCs to form micelles, the polymeric surfactants formed micelles without any indication of CMC from the surface tension measurement studies. That means the polymeric surfactants do not need minimum amount of polymeric surfactants to form aggregated structures (micelles) because the polymeric surfactants already exist as aggregated structures by chemical bond linkage (polymerization) of their monomers (about 100 monomeric surfactants)
- Bakeev KN, Ponomarenko EA, Shishanova TV, Tirrell DA, Zezin AB, Kabanov VA, Macromolecules, 28(8), 2886 (1995)
- Laschewsky A, Colloid Polym. Sci., 269, 785 (1991)
- Abid SK, Sherrington DC, Polymer, 33, 175 (1992)
- Loffer R, Richtering WH, Finkelmann H, Burchard W, J. Phys. Chem., 96, 3883 (1992)
- Blum FD, Durairaj B, Langmuir, 5, 370 (1989)
- Nagai K, Satoh H, Kuramoto N, Polymer, 33, 5303 (1992)
- Steven MP, Polymer Chemistry An Introduction, 204 Oxford Univ. Press, New York (1990)
- Glatzhofer DT, Cho G, Chung L, O'Rear ED, Fung BM, Langmuir, 9, 2949 (1993)
- Gambogi RJ, Blum FD, J. Colloid Interface Sci., 140, 525 (1990)
- Langmuir I, J. Am. Chem. Soc., 39, 1848 (1917)
- Langmuir I, J. Chem. Phys., 1, 756 (1933)
- McBain JW, Adv. Colloid Sci., 1, 99 (1942)
- Klevens HB, Chem. Rev., 1, 47 (1950)
- Christian SD, Smith GA, Tucker EE, Scamehorn JF, Langmuir, 1, 564 (1985)
- Smith GA, Christian SD, Tucker EE, Scamehorn JF, J. Solution Chem., 15, 519 (1986)
- Sasaki KJ, Burnett SJ, Christian SD, Tucker EE, Scamehorn JF, Langmuir, 3, 548 (1987)
- Christian SD, Tucker EE, Scamehorn JF, Lee BH, Sasaki KJ, Langmuir, 5, 876 (1989)
- Mamoud FJ, Christian SD, Tucker EE, Taha A, Scamehorn JF, J. Phys. Chem., 93, 5903 (1989)
- Lee BH, Ph.D. Dissertation, The University of Oklahoma (1990)
- Lee BH, Christian SD, Tucker EE, Scamehorn JF, J. Phys. Chem., 59, 360 (1991)
- Paleso CM, Stassinopoulous CI, Mailaris A, J. Phys. Chem., 87, 251 (1983)
- Goto A, Endo E, J. Colloid Interface Sci., 66, 26 (1978)
- Hoiland H, Ljosland E, Backund S, J. Colloid Interface Sci., 101, 467 (1984)
- Treiner C, Chattopadhyay AK, J. Colloid Interface Sci., 109, 101 (1986)
- Bhat SN, Smith GA, Tucker EE, Christian SD, Scamehorn JF, Smith W, Ind. Eng. Chem. Res., 26, 1217 (1987)
- Uchiyama H, Christian SD, Scamehorn JF, Abe M, Ogino K, Langmuir, 7, 95 (1991)
- Christian SD, Tucker EE, Scamehorn JF, Uchiyama H, Colloid Polym. Sci., 271, 745 (1994)
- Dunaway CS, Christian SD, Tucker EE, Scamehorn JF, In Solubilization in Surfactant Aggregatesy, Christian, S.D. Scamehorn and J.F. (eds.), 8, Marcek Dekker, New York (1989)
- Uchiyama H, Christian SD, Tucker EE, Scamehorn JF, J. Colloid Interface Sci., 163(2), 493 (1994)
- Smith GA, Ph.D. Dissertation, University of Oklahoma (1986)
- Lee BH, Christian SD, Tucker EE, Scamehorn JF, Langmuir, 6, 230 (1990)
- Ruthman JF, Scamehorn JF, J. Phys. Chem., 88, 5807 (1984)
- Nishikido N, Langmuir, 7, 2876 (1991)
- Dum RO, Scamehorn JF, Christian SD, Sep. Sci. Technol., 20, 257 (1985)
- Lee BH, Christian SD, Tucker EE, Scamehorn JF, Langmuir, 7, 1332 (1991)
- Kandori K, McGreevy RJ, Schchfer RS, J. Colloid Interface Sci., 132, 395 (1989)