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Point of Zero Salt Effect: Relationships with Clay Mineralogy of Representative Soils of the So Paulo State, Brazil 被引量:2

Point of Zero Salt Effect: Relationships with Clay Mineralogy of Representative Soils of the So Paulo State, Brazil
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摘要 The point of zero salt effect (PZSE) is the soil pH value at which the magnitude of the variable surface charges is notchanged due to variations in the ionic concentration of the soil solution. This property influences not only electrochemicalphenomena occurring at the solid-solution interface but also the flocculation degree of the soil particles. In this studywe investigated the relationships between the clay mineralogy and the PZSE values of representative soils of the S?oPaulo State, Brazil. The results confirmed the usefulness of the difference between the soil pH values measured in 1 molL-1 KCl (pHKCl) and in water for estimating the PZSE of tropical soils, except for theones rich in exchangeable Al; furthermore, the ΔpH index was highly correlated with the differencebetween the PZSE and values, reiterating the ΔpH utility for estimating both the signal and the magnitude of thenet surface charge of tropical soils. Finally, correlation and multiple regression analyses showed that the PZSE value ofweathered non-allophanic tropical soils tends to increase and to equal the soil pH due to the weathering-induced kaolinitedestabilization and concomitant Fe- and Al-oxide accumulation. The point of zero salt effect (PZSE) is the soil pH value at which the magnitude of the variable surface charges is not changed due to variations in the ionic concentration of the soil solution. This property influences not only electrochemical phenomena occurring at the solid-solution interface but also the flocculation degree of the soil particles. In this study we investigated the relationships between the clay mineralogy and the PZSE values of representative soils of the Sāo Paulo State, Brazil. The results confirmed the usefulness of the difference between the soil pH values measured in 1 mol L^-1 KCl (pHKCl) and in water (pHH2O) (2 pHKCl-pHH2O) for estimating the PZSE of tropical soils, except for the ones rich in exchangeable Al; furthermore, the ApH index (pHKC1 - pHH2O) was highly correlated with the difference between the PZSE and pHH2O values, reiterating the △pH utility for estimating both the signal and the magnitude of the net surface charge of tropical soils. Finally, correlation and multiple regression analyses showed that the PZSE value of weathered non-allophanic tropical soils tends to increase and to equal the soil pH due to the weathering-induced kaolinite destabilization and concomitant Fe- and Al-oxide accumulation.
出处 《Pedosphere》 SCIE CAS CSCD 2005年第5期545-553,共9页 土壤圈(英文版)
基金 the State of So Paulo Research Foundation-FAPESP, Brazil (No. 98/01502-8).
关键词 PZSE 土壤 pH值 巴西 电化学 electrochemical properties, iron oxides, kaolinite, tropical soils, weathered soils
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  • 1Alves, M. E., Macedonio, C. R. and Lavorenti, A. 2002. Point of zero salt effect: Analytical-computational approach to its determination from potentiometric titration data. Brazilian Journal of Soil Science (in Portuguese). 26: 553-559.
  • 2Bertsch, P. M. and Bloom, P. R. 1996. Aluminium. In Sparks, D. L. (ed.) Methods of Soil Analysis. Part 3. Chemical Methods. American Society of Agronomy and Soil Science Society of America, Madison. pp. 517-550.
  • 3Buurman, P., Van Lagen, B. and Velthorst, E. J. 1996. Manual for Soil and Water Analysis. Backhuys Publishers, Leiden.314pp.
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  • 8Fontes, M. P. F. 1992. Iron oxide-clay mineral association in Brazilian oxisols: A magnetic separation study. Clays and Clay Minerals. 40: 175-179.
  • 9Gee, G. W. and Bauder, J. W. 1986. Particle size analysis. In Klute, A. (ed.) Methods of Soil Analysis. Part 1. Physical and Mineralogical Methods. American Society of Agronomy and Soil Science Society of America, Madison. pp.383-409.
  • 10Hendershot, W. H. and Lavkulich, L. M. 1979. Effect of sodium-chloride saturation and organic matter removal on the value of zero-point of charge. Soil Science. 128: 136-141.

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