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Buffer Intensities and Equilibrium pH of Minerals and Soils: II. Theoretical and Actual pH of Minerals and Soils
Author(s) -
Breemen N.,
Wielemaker W. G.
Publication year - 1974
Publication title -
soil science society of america journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.836
H-Index - 168
eISSN - 1435-0661
pISSN - 0361-5995
DOI - 10.2136/sssaj1974.03615995003800010023x
Subject(s) - gibbsite , soil water , kaolinite , illite , chemistry , clay minerals , montmorillonite , allophane , lime , mineral , soil ph , calcite , oxide minerals , inorganic chemistry , mineralogy , environmental chemistry , geology , soil science , chemical reaction , paleontology , organic chemistry , biochemistry
Equilibrium pH values of different clay minerals, oxides and carbonates at pCO 2 = 10 ‐2 atm. are between 4.5 and 8, i.e., in the range typical for most soils. The agreement between the calculated pH and the abrasion pH for most minerals is reasonable. The pH of a number of soils can be explained by partial equilibrium between the soil solution and kaolinite, allophane, gibbsite, montmorillonite or calcite. For illite the agreement is less satisfactory. The effects of reducing conditions and the possible role of pH buffering by organic matter are discussed briefly. Application of the phase rule indicates that the specific mineral assemblage of acid sulfate soils provides a nearly ideal pH‐stat, i.e., addition of moderate amounts of sulfuric acid or lime hardly affects the pH.