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ABSTRACT
The chemical forms which zinc assumes when added to soils and clays have been investigated, using the isotope dilution technique (with Zn65 as a tracer). After equilibrium, the added zinc was extracted by successive leaching with neutral normal NH4Ac, 2.5% HAc, and 0.1 N HCl. Variables were: (1) time of equilibrium, (2) calcium saturation, (3) amount of zinc added, (4) rate of extraction, and (5) type of clay mineral.
With symmetry additions of zinc and a hydrogen soil system, practically all of the zinc taken up by the soil was replaceable with NH4Ac, whereas in a calcium soil system a part of the zinc could not be replaced with NH4Ac. The portion of the zinc not removed with NH4Ac could be extracted by repeated leaching with dilute HCl. This acid-soluble form of zinc increased with increasing length of time of contact between the soil and the zinc solution. It apparently did not occupy exchange sites in the soils, since there was no reduction in the base-exchange capacity of the soil with the formation of the acid-soluble form. As smaller quantities of zinc were added to these soils and as the amount of time following the addition increased, a higher proportion of the zinc was found in the acid-soluble form.
1 Contributed from the Department of Agronomy, Illinois Agr. Exp. Sta., Urbana, Ill. Published with the approval of the Director. Presented before Div. II, Soil Science Society of America, St. Paul, Minn., Nov. 9, 1954. This work was submitted by the senior author as part of a thesis in partial fulfillment of requirements for the Ph.D. degree. The support of International Minerals and Chemicals Corp. in this work is gratefully acknowledged.
2 Former Research Assistant at University of Illinois, now Agent (Soil Scientist), Soil and Water Conservation Research Branch, A.R.S., U.S.D.A., Prosser, Wash., and Associate Professor, University of Illinois.
Received for publication November 4, 1954.
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