Simultaneous measurement of exchangeable Al and other cations in acidic soils

Abstract

It is both time consuming and costly to undertake two extractions of acidic soils when there is a need to measure exchangeable Al along with the other cations. There is some evidence that, although 1 M KCl is the standard procedure for exchangeable Al, the extraction of soil with 0.1 M BaCl2 + 0.1 M NH4Cl gives similar values. It would then be possible to measure all cations from one extraction. There is also concern that the assumption of trivalence of Al does not hold true in all situations, as commonly held to be true in the literature of the 1950s to the 1970s. Two experiments were conducted: the first a simple comparison of three extraction procedures in common use in New South Wales and the second a repeated comparison of two extractions but with more detailed measurements to enable interpretation of the results. During the second experiment we also measured the charge on the extracted Al by titration. The three methods for extraction of Al gave similar results despite very different procedures with respect to physical mixing, soil–solution contact time and strength of electrolyte, indicating that the pool of exchangeable Al was operationally well defined. The average charge on KCl-extracted Al was within error of 3 moles per mole of Al, supporting the current trivalent model of Alex. The 0.1 M BaCl2 + 0.1 M NH4Cl procedure estimated Alex successfully on acid soils of low effective cation exchange capacity (ECEC) (<10 cmolc/kg) and so can be used for extraction of all cations. However, as ECEC increased the 0.1 M BaCl2 + 0.1 M NH4Cl extraction tended to underestimate Alex compared with KCl on soils with above ~1.5 to 2 cmolc/kg of Alex.