A D S O R P T I O N OF P O T A S S I U M AS INFLUENCED BY C O N C E N T R A T I O N A N D p H OF THE SOL UTIO N By S. P. MITRA and DHARAMPRAKASH, Sheila Dhar Institute of Soil Science, University of Allahabad, India. [MS. Received 30th October, 1956.] ABSTRACT The adsorption of potassium by clay minerals under varying conditions of concentration and pH has been studied. It seems from the experimental data that montmoriUonite shows the greatest adsorption at all pH values. The adsorption is found to vary with the concentration of potassium in the solution, pH of the solution and the nature of the cations in the exchange complex. Data are presented for kaolinite, montmorillonite, halloysite and natrolite. INTRODUCTION It is well known that clay minerals adsorb certain cations such as K +, NH4 + and Rb +. The present paper includes some studies on the adsorption of potassium by some minerals at different concentrations from solutions of KH2PO4, K2HPO4 and KzPO4, i.e., within a p H range of 5.2 to 11-8. EXPERIMENTAL The adsorption experiments were conducted on the ovendried samples. Four g of minerals were treated with KH2PO4, K2HPO4 and K~PO4 solutions of varying concentrations, shaken for an hour in a mechanical shaker, kept for two days and filtered through a buchner funnel. The clear filtrate was analyzed for potassium which was estimated as potassium sodium cobaltinitrite. DISCUSSION The results in Table 1 clearly show the adsorption of potassium by montmorillonite, kaolinite, halloysite and natrolite, both from acid and alkaline salts of potassium of concentrations varying from 0.02 M to 0.001 M. The adsorption is a function of concentration. It decreases with a decrease in the concentration of the salt added. The decrease in the amount of potash adsorbed is only proportional in a few cases to the decrease in concentration. Montmorillonite adsorbs the greatest amount of potassium at p H values from 5.2 to 151 152 S. P. MITRA A N D D. PRAKASH o 9~,~ ~ o ~ o ~ e.qOOlP~.~-~, 0 0 0 0 0 0 ~'~0 4, 0 % 0 o ~ _o ~o~ 9. - ~ ~ t ~ . o o 0 ~'~0 = im 0 0 E 0 0 ~'~0 .< < 0 0 .,e , ~. ~00 O~"g~0 0 0 0 0 0 O0 O~o 0 < POTASSIUM ADSORPTION BY CLAYS 153 11-8, while kaolinite and halloysite adsorb a much smaller amount. Natrolite adsorbs a greater amount of potassium than either kaolinite or halloysite. It seems that generally the adsorption of potassium is greater in an alkaline medium than in an acid medium. The type of cation dominant in the exchange complex also seems to influence the ability of the mineral to adsorb potassium, for Wiklander, (1950) who studied the fixation of potassium by clays saturated with different cations, found that if Ca z+, Mg 2+, Na +, etc., were the ions already present, they could be replaced by K +, while this replacement was more difficult if NH4 + or H + were the cations already present. It has also been shown by Peech and Bradfield (1934) that the abilities of the soils to adsorb potassium from neutral salts decreased as the degree of base saturation decreased. Kashmir montmorillonite contains a very high percentage of exchangeable calcium and the high amount of calcium seems to be very effective in increasing the adsorption of potassium by montmorillonite. This is further supported by the results obtained by Ayers (1941) for the adsorption of potassium at various degrees of calcium saturation by the Hilo-Coast soil. The results indicate that increasing the amounts of exchangeable calcium in the soil irtereases its ability to adsorb K +. Gilligan (1938), Harris (1937) and McIntire (1936) have demonstrated that liming increases the adsorption and fixation of potassium. Although the present work does not lead to any definite conclusion as some other factors are undoubtedly involved, for the b.e.c, of montmorillonite is considerably above that of the other minerals and the role of anion adsorption is difficult to evaluate, yet it appears definite that the adsorption of potassium is related to the exchangeable calcium content of the mineral, and this in turn is presumably in some manner linked with the anion adsorption. REFERENCES Ayers, A. S. 1941. Soil Sci., 51, 265. Gilligan, G. M. 1938. Bull. DeL Agr. Exp. Sta, 215, 1-20. Harris, H. C. 1937. SoilSci., 44, 265-75. MacIntire, W. H. 1936. J. Amer. Soc. Agron., 2.8, 202-15. Peech, M. and Bradfield, R. 1934. Bull. Amer. Soil surv. Assn., 15, 10l-6. Wiklander, L. 1950. Soil ScL, 69, 261-8.
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