The sorption at room temperature of benzene and naphthalene from water and from methanolwater mixtures by four different organophilic clays has been determined. The organophilic clays were prepared from Wyoming montmorillonite by replacing the natural exchange ions of the clay by the quaternary ammonium ions TMA (tetramethylammonium), TMPA (trimethylphenylammonium), HDTMA (hexadecyltrimethylammonium), and BDTDA (benzyldimethyltetradecylammonium). Of these organoclays, TMPA-montmorillonite has the greatest sorptive ability for naphthalene and is followed in order of decreasing sorptive ability by BDTDA-, HDTMA-, and TMA-montmorillonite.
Principal Investigator: Evangelos A. Voudrias (Georgia Institute of Technology)
Principal Investigator: J. M. Wampler (Georgia Institute of Technology)
Principal Investigator: Charles E. Weaver (Georgia Institute of Technology)
Sponsor: GWRI
Start Date: 1992-04-01; Completion Date: 1993-03-31;
Keywords: Organoclays, Quaternary ammonium ions, Clay minerals, Montmorillonite, Sorption, Adsorption and exchange, Aromatic hydrocarbons, Organic wastes, Wastewater treatment
Description:
The sorption at room temperature of benzene and naphthalene from water and from methanolwater mixtures by four different organophilic clays has been determined. The organophilic clays were prepared from Wyoming montmorillonite by replacing the natural exchange ions of the clay by the quaternary ammonium ions TMA (tetramethylammonium), TMPA (trimethylphenylammonium), HDTMA (hexadecyltrimethylammonium), and BDTDA (benzyldimethyltetradecylammonium). Of these organoclays, TMPA-montmorillonite has the greatest sorptive ability for naphthalene and is followed in order of decreasing sorptive ability by BDTDA-, HDTMA-, and TMA-montmorillonite. TMA-montmorillonite is much more effective as a sorbent for benzene than it is for naphthalene. For benzene sorption, TMPA-montmorillonite is most effective, followed in order by TMA- and BDTDA-montmorillonite. The presence of methanol as a co solvent reduces the sorption coefficients in the manner predicted by the solvophobic theory of Rao et al. (1985), that is, the sorption coefficients decrease approximately in log-linear fashion as the methanol content increases, but the decrease in the sorption coefficients is generally less than that to be expected because of increasing solubility of the sorbate with increasing methanol content (that is, the value of a is less than 1). As others have shown, the form of the isotherms for sorption of benzene and naphthalene from water by organoclays having small quaternary ammonium ions (TMA and TMP A) indicates that adsorption is the primary mechanism of sorption. Organoclays having a long-chain alkyl substituent on the organic cation (BDTDA- and HDTMA-montmorillonite) sorb by a mechanism that is essentially partitioning of the sorbate between water and the organic material in the clay interlayers. The cosolvent methanol affects the form of the isotherms, causing the isotherms to become progressively closer to linear form as the fraction of methanol in the liquid phase increases. This observation is interpreted to indicate that the partitioning mechanism of sorption becomes predominant as the methanol content of the solvent increases. Isotherms obtained from single-step desorption experiments indicate that sorbed naphthalene reaches equilibrium with fresh methanol-rich solvent in less than 48 hours, but if the volume fraction of methanol is 30% or less, such equilibrium may not be achieved in 48 hours.