Fx. Han et A. Banin, SELECTIVE SEQUENTIAL DISSOLUTION TECHNIQUES FOR TRACE-METALS IN ARID-ZONE SOILS - THE CARBONATE DISSOLUTION STEP, Communications in soil science and plant analysis, 26(3-4), 1995, pp. 553-576
Dissolution capacity and kinetics of carbonates by sodium acetate (NaO
Ac)-acetic acid (HOAc) at various pHs were studied. A comparative stud
y of the selectivity, specificity, and effectivity of NaOAc-HOAc solut
ion on carbonate bound fraction during the sequential selective dissol
ution procedure was conducted by comparing the dissolution of major an
d trace elements from arid zone soils by this buffer solution at vario
us pHs. The effect of the pH of NaOAc-HOAc solution on the following f
ractions in the sequential selective dissolution procedure was also st
udied. NaOAc-HOAc solution at pH 5.5 at a soil to solution ratio of 1:
25, can dissolve all the carbonate from calcareous soils with .10-20%
of carbonate; at pH 5.0 it can dissolve all the carbonate in soils wit
h about 30-50% calcium carbonate (CaCO3). A second era-action with fre
sh buffer solution at pH 5.0 is required for soils with more than 50%
of carbonate. Six hours of extraction time is generally sufficient for
complete carbonate dissolution. For most of agricultural soils in ari
d and semi-arid zones, the attack of the buffer solution at pH 5.0 on
other solid-phases seems to be limited. But the buffer solution at pH
5.5 would be better for some forest soils with low carbonate content a
nd high organic matter content. The part of carbonate fraction not be
dissolved in this step is released in the following steps: easily redu
cible oxides fraction (ERO), organic matter fraction (OM), and reducib
le oxides fraction (RO), leading to gross misinterpretation of the ele
mental partitioning in arid zone soils.