1995•Journal of the Indian Society of Soil ScienceOpen access

Ph~sphorus Sorption as Influenced by Soil Clay Minerals in Major Soil Groups of India

K.P. Tomar, Attinti Ramesh, A.K. Biswas

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Abstract

Sorption envelopes (pH 4.2 to 8.0) of ten soils representative of various soil groups of India at 3.23, 6.45, 12.9 and 25.8 mmol P kg−1 soil levels in 0.01M CaCl2 matrix solution were studied. At low P levels, kaolinite dominant soils sorbed highest amount of P followed by illite and 2:1 expanding layer mineral dominated soils. This was attributed to spilling over of negative charge from basal planes to edge face region in 2:1 expanding layer minerals and to a lesser extent in illite, which weakened the attractive forces between the positively charged edge face of 2:1 minerals and phosphate. The above sequence of P adsorption changed at high P rates. This was ascribed to electrostatic adsorption on low affinity sites, which are abundant in 2:1 expansible layer minerals. The acidic soils sorbed less than 60% of added P at low pH and greater than 99% at high pH compared to non-acid soils (86% and 84%, respectively). This peculiar behaviour is ascribed to increasing polymerization of exch. A13+ with increase in pH. P sorption was not influenced by any soil constituent other than free iron oxides, exch. Al3+ and clay minerals.

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Sorption envelopes (pH 4.2 to 8.0) of ten soils representative of various soil groups of India at 3.23, 6.45, 12.9 and 25.8 mmol P kg−1 soil levels in 0.01M CaCl2 matrix solution were studied. At low P levels, kaolinite dominant soils sorbed highest amount of P followed by illite and 2:1 expanding layer mineral dominated soils. This was attributed to spilling over of negative charge from basal planes to edge face region in 2:1 expanding layer minerals and to a lesser extent in illite, which weakened the attractive forces between the positively charged edge face of 2:1 minerals and phosphate. The above sequence of P adsorption changed at high P rates. This was ascribed to electrostatic adsorption on low affinity sites, which are abundant in 2:1 expansible layer minerals. The acidic soils sorbed less than 60% of added P at low pH and greater than 99% at high pH compared to non-acid soils (86% and 84%, respectively). This peculiar behaviour is ascribed to increasing polymerization of exch. A13+ with increase in pH. P sorption was not influenced by any soil constituent other than free iron oxides, exch. Al3+ and clay minerals.

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Available abstract

Sorption envelopes (pH 4.2 to 8.0) of ten soils representative of various soil groups of India at 3.23, 6.45, 12.9 and 25.8 mmol P kg−1 soil levels in 0.01M CaCl2 matrix solution were studied. At low P levels, kaolinite dominant soils sorbed highest amount of P followed by illite and 2:1 expanding layer mineral dominated soils. This was attributed to spilling over of negative charge from basal planes to edge face region in 2:1 expanding layer minerals and to a lesser extent in illite, which weakened the attractive forces between the positively charged edge face of 2:1 minerals and phosphate. The above sequence of P adsorption changed at high P rates. This was ascribed to electrostatic adsorption on low affinity sites, which are abundant in 2:1 expansible layer minerals. The acidic soils sorbed less than 60% of added P at low pH and greater than 99% at high pH compared to non-acid soils (86% and 84%, respectively). This peculiar behaviour is ascribed to increasing polymerization of exch. A13+ with increase in pH. P sorption was not influenced by any soil constituent other than free iron oxides, exch. Al3+ and clay minerals.

Key concepts: Illite, Sorption, Clay minerals, Soil water, Kaolinite, Adsorption, Chemistry, Environmental chemistry

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