101. Electrochemical Properties of Latosols with Different Mineralogies.
- Author
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Pinheiro, Ronaldo Batista, Cantarutti, Reinaldo Bertola, Villani, Ecila Mercês de Albuquerque, Cavalcante, Valéria Santos, and Fontes, Maurício Paulo Ferreira
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FERRALSOLS , *POINTS of zero charge , *MINERALOGY , *POTENTIOMETRY , *OXISOLS - Abstract
Studying the electrochemical behavior of colloidal particles is important for fertility management and soil conservation, since it enables the understanding of several physicochemical phenomena that occur in soils. The objective of this study was to determine the point of zero charge (PZC) and the electrochemical behavior of surface and subsurface samples of three Red-Yellow Latosols (Oxisols), with different mineralogical and textural characteristics, through potentiometric titration and ionic adsorption. The point of zero charge (PZC) and the electrochemical behavior were determined in samples from the A and B horizons of three Red-Yellow Latosols: very clayey kaolinitic (LVAcr), very clayey gibbsitic (LVAgr) and sandy loam kaolinitic (LVAcm). The analyses were conducted in soil samples with particle size smaller than 0.7 mm, with desaturation of aluminum (Al3+), and smaller than 2 mm, without desaturation. Solutions containing sodium (Na+) and nitrate (NO3−) as indifferent electrolytes were used in all methods. The LVAgr, even with higher organic matter contents, had higher PZC, indicating the importance of mineralogical composition for this characteristic. Among the two kaolinitic soils, there was higher PZC in LVAcm, with lower organic matter content; however, both soils had higher PZC in the B horizon than in the A horizon. The net electrical charge estimated by the potentiometric titration method was equivalent to the net charge estimated by the ionic adsorption method for horizons A and B of LVAgr and LVAcm. At the same time, there was underestimation of the net negative charge by the potentiometric titration method for the A and B horizons of LVAcr. [ABSTRACT FROM AUTHOR]
- Published
- 2022
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