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Effect of Different Factors on the Adsorption of Phosphamidon on Two Different Types of Indian Soil
Author(s) -
D. P. Singh
Publication year - 1998
Publication title -
adsorption science and technology
Language(s) - English
Resource type - Journals
eISSN - 2048-4038
pISSN - 0263-6174
DOI - 10.1177/026361749801600801
Subject(s) - chemistry , loam , adsorption , cation exchange capacity , freundlich equation , organic matter , phosphamidon , soil water , soil organic matter , silt , soil science , organic chemistry , agronomy , geology , dimethoate , pesticide , biology , paleontology
The effect of exchangeable cations (H + and Na + ). autoclaving, organic matter, anionic surfactants and temperature on the adsorption of phosphamidon on two different types of Indian soil was studied. The adsorption isotherms for all the effects/treatments were in close agreement with the Freundlich equation and yielded S-shaped isotherms. The amount of phosphamidon adsorbed in all cases was higher in medium black (silt loam) soil than alluvial soil (sandy loam) and was related to the organic matter content, clay content, CaCO 3 content, surface area and cation-exchange capacity of the soils. The adsorption on both types of soil follows the order H + -soil > Na + -soil > natural soil at 10°C > natural soil at 20°C > autoclaved soil > organic matter-removed soil > anionic surfactant > natural soil at 40°C, which was in accordance with the Freundlich constant, K F , and distribution coefficient, K d , values. The adsorption capacity of phosphamidon for organic matter and clay content for both the soils was evaluated by calculating the K om and K c values when it was found that phosphamidon adsorption was better correlated with the clay content than with the orgnic matter content on the basis of adsorption isotherms. Various thermodynamic parameters such as the thermodynamic equilibrium constant (K 0 ), the standard free energy (ΔG 0 ), the standard enthalpy (ΔH 0 ) and the standard entropy (ΔS 0 ) changes have been calculated as a means of predicting the nature of the isotherms.

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