Clay-Organic Complexes as Adsorbents for Phenol and Chlorophenols1

Max M. Mortland, Sun Shaobai2 and Stephen A. Boyd
Department of Crop and Soil Sciences, Michigan State University East Lansing, Michigan 48824
1 Contribution of the Michigan Agricultural Experiment Station, East Lansing, Michigan 48824, Journal Article No. 11972.
2 Visiting scientist, Sichuan Agricultural University, Peoples Republic of China.

Abstract: Several clay-organic complexes were synthesized by placing quaternary ammonium cations on smectite by cation exchange. They were then examined for their ability to adsorb phenol and several of its chlorinated congeners. The organic cations used were: hexadecylpyridinium (HDPY+), hexadecyltrimethyl ammonium (HDTMA+), trimethylphenyl ammonium (TMPA+), and tetramethylammonium (TMA+). The complexes containing long-chain alkyl (hexadecyl) groups were the most hydrophobic and adsorbed the phenols from water in proportion to their hydrophobicities, which increase with chlorine addition (phenol < chlorophenol < dichloropohenol < trichlorophenol). With n-hexane as the solvent, different adsorption was found which depended on the type and degree of solvent interactions with the compound and the clay-organic complex. Thus, the amount of adsorption of these phenols on clay-organic complexes was dependent on the relative energies of adsorbent-adsorbate and adsorbate-solvent interactions.

Key Words: Adsorption • Chlorophenols • Hydrophobicity • Organo clays • Phenol • Smectite

Clays and Clay Minerals; October 1986 v. 34; no. 5; p. 581-585; DOI: 10.1346/CCMN.1986.0340512
© 1986, The Clay Minerals Society
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