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Peptization Resistance of Selected Samples of Kaolinitic, Montmorillonitic, and Illitic Clay Materials

Published online by Cambridge University Press:  01 January 2024

U. Grant Whitehouse
Affiliation:
Agricultural and Mechanical College of Texas, USA
Lela M. Jeffrey
Affiliation:
Agricultural and Mechanical College of Texas, USA

Abstract

Variations in the peptization resistance of selected samples of clay mineralogical materials toward alkaline dispersing agents are discussed from a quantitative point of view.

Clay samples, collected from South Carolina, Wyoming, Illinois, New Mexico, South Wales, Great Britain and Cornwall, England were subjected to the action of solutions of Calgon (“sodium hexametaphosphate”), ammonia, sodium hydroxide, sodium carbonate, sodium pyrophosphate, and “sodium lignosulfonate.” The resulting apparent dispersion, in each case, was expressed as a function of the employed concentration and chemical nature of the dispersing agent. Pipette analysis and Oden balance techniques at constant temperature were used to measure the degree of dispersion. All clay samples employed were identified as to type by X-ray diffraction, chemical analysis, thermal analysis, and electron microscopy.

All samples examined exhibited a maximum in apparent dispersion (suspension stability) at a specific concentration of dispersing agent. Such maximum was followed by a sudden decrease in apparent dispersion, i.e., flocculation, at higher concentrations of dispersing agent. Concentrations of dispersing agent were varied in steps of one part per thousand. One hundred and twenty experimental runs were made on each type of material examined. Differences in the degree of apparent dispersion attained by use of different dispersing agents were expressed in terms of a threshold concentration which altered “equivalent diameter” one tenth of a phi unit. Among dispersing agents employed, “sodium lignosulfonate” was found to be least selective of clay mineral type in its peptizing action.

An equation for the calculation of a “peptization resistance factor” is presented. Results obtained by application of this equation indicate that differences in the response of the same clay material to different alkaline dispersing agents may be attributed, in part, to differences in degree of peptization achieved by “threshold mechanisms” of peptization and by “adjustment mechanisms” along the peptization path. Such equation may have future value in the differentiation of marine and terrestrial clay deposits.

Type
Article
Copyright
Copyright © The Clay Minerals Society 1954

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Footnotes

A contribution from the Chemical Division of the Department of Oceanography, A. and M. College of Texas, College Station, Texas, Oceanographic and Meteorological Series No. 57.

References

Atterberg, A. (1905) Die rationelle klassifikation der sande und kiese: Chem. Zeitung, Bd. 29, pp. 195198.Google Scholar
Bancroft, W. D. (1952) Applied colloid chemistry, third edition, McGraw-Hill Book Co., New York.Google Scholar
Bowden, W. C. Jr. (1950) Analytical data on reference class minerals. Part B. Chemical analysis: Amer. Petroleum Inst. Proj. 49 Prelim. Report, pp. 3841.Google Scholar
Bungenberg de Jong, H. G. (1937) Wissenschaftliche und technische sammelreterate. II. Koazervation: Koll. Zeit., Bd. 80, pp. 221230.CrossRefGoogle Scholar
Coffman, P. M. (1946) Base exchange capacities of clays: M. A. Thesis, Stanford Univ.Google Scholar
Freundlich, H. (1932) Kappilarchemie, vol. 1, second ed.: Akademishe Verlagsgesell- shaft, Leipzig, p. 735.Google Scholar
Grim, R. E. (1951) Specific methods of analysis, method and application of differential thermal analysis: Ann. New York Acad. Sei., vol. 53, pp. 9951118.Google Scholar
Hamaker, H. (1937) Symposium of Lyophobic Colloids: Utrecht, p. 16.Google Scholar
Hauser, E. A. (1951) Modern colloid chemical concepts of the phenomenon of coagulation: Jour. Phy. and Coll. Chem., vol. 55, p. 608.Google ScholarPubMed
Hillebrand, W. F. et al. (1953) Applied inorganic analysis: John Wiley and Sons, Inc.Google Scholar
Krumbein, W. C. (1934) Size frequency distributions of sediments: Jour. Sed. Petrology, vol. 4, pp. 6577.Google Scholar
Krumbein, W. C. (1937) Korngrosseneinteilungen und statistische analyse: Neues Jahrb. f. Min., etc., Beil.-Bd. 73. Abt. A, pp. 137150.Google Scholar
Krumbein, W. C., and Pettijohn, F. J. (1938) Manual of sedimentary petrography: Appleton-Century-Crofts, Inc., New York.Google Scholar
Kruyt, H. R., and Van Klooster, H. S. (1927) Colloids: John Wiley and Sons, Inc., New York, pp. 6768.Google Scholar
Langmuir, I. (1938) The role of attractive and repulsive forces in the formation of tactoids, thixotropic gels, protein crystals, and coacervales: Jour. Chem. Physics, vol. 6, p. 873.CrossRefGoogle Scholar
McBain, J. W. (1950) Colloid science: D. C. Heath and Co., Boston, p. 380.Google Scholar
Mecklenberg, W. (1912) Zur isomerie der zinnsauren: Zeit, Anorg. Chemie, Bd. 74, p. 207.CrossRefGoogle Scholar
Oden, S. (1915) Eine neue methode zur mechanischen boden analyse: Int. Mitt. fur Bodenkunde, Bd. 6, pp. 257311Google Scholar
Ostwald, W. (1927) Zur theorie der boden körperregel: Koll. Zeit., Bd. 43, p. 249.CrossRefGoogle Scholar
Stokes, G. G. (1851) On the effect of the internal friction of fluids on the motion of pendulums: Trans. Cambridge Philos. Soc., vol. 9, part 2, pp. 8106.Google Scholar
Teichert, W., et al. (1948) Beitrag zur kenntnis der natrium metaphosphate. Parts I and II: Acta Chem. Scand., Bd. 2, pp. 225 and 414.CrossRefGoogle Scholar
Teichert, W., et al. (1949) Beitrag zur kenntnis der natrium metaphosphate. Part III: Acta Chem. Scand., Bd. 3, p. 72.CrossRefGoogle Scholar
Thiessen, P. A. (1942) Wechselseitige adsorption von kolloiden: Zeit. Electrochem., Bd. 48, p. 675.Google Scholar
Thomas, A. W. (1934) Colloid chemistry, McGraw-Hill Book Co., New York, p. 65.Google Scholar
Udden, J. A. (1914) Mechanical composition of clastic sediments: Geol. Soc. America Bulletin, vol. 25, pp. 655744.Google Scholar
Van Olphen, H. (1950) Stabilization of montmorillonite sols by chemical treatment. Parts I and II: Recueil des travaux chimiques des Pays-Bas, vol. 69, pp. 13081322.CrossRefGoogle Scholar
Vervey, E. J. W., and Overbeek, J. T. G. (1948) Theory of the stability of lyophobic sols: Elsevier Publ. Co., Amsterdam.Google Scholar
Von Weimarn, P. P. (1914) Grundsuge der dispersoid chemie: Th. Steinkopff, Dresden.Google Scholar
Wadell, H. (1936) Some practical sedimentation formulas: Geol. Fören Forhändl, vol. 58, pp. 297408.Google Scholar
Weiser, H. B. (1949) Colloid chemistry, 2nd edition, John Wiley and Sons., Inc., New York, p. 153.Google Scholar
Wentworth, C. K. (1922) A scale of grade and class terms for clastic sediments: Jour. Geol., vol. 30, pp. 377392.CrossRefGoogle Scholar
Zsigmondy, R. (1909) Colloids and the ultramicroscope, translated by Alexander, J., John Wiley and Sons, New York.Google Scholar