4.7 Article

The citric acid-MnIII,IVO2(birnessite) reaction.: Electron transfer, complex formation, and autocatalytic feedback

Journal

GEOCHIMICA ET COSMOCHIMICA ACTA
Volume 70, Issue 17, Pages 4463-4476

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.gca.2006.06.1551

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Citrate released by plants, bacteria, and fungi into soils is subject to abiotic oxidation by MnO2(birnessite), yielding 3-ketoglutarate, acetoacetate, and MO. Citrate loss and generation of products as a function of time all yield S-shaped curves, indicating autocatalysis. Increasing the citrate concentration decreases the induction period. The maximum rate (r(max)) along the reaction coordinate follows a Langmuir-Hinshelwood dependence on citrate concentration. Increases in pH decrease rmax and increase the induction time. Adding Mn-II, Zn-II, orthophosphate, or pyrophosphate at the onset of reaction decreases r(max.) Mn-II addition eliminates the induction period, while orthophosphate and pyrophosphate addition increase the induction period. These findings indicate that two parallel processes are responsible. The first, relatively slow process involves the oxidation of free citrate by surface-bound Mn-III,Mn-IV yielding Mn-II and citrate oxidation products. The second process, which is subject to strong positive feedback, involves electron transfer from Mn-II-citrate complexes to surface-bound Mn-III,Mn-IV, generating Mn-III-citrate and Mn-II Subsequent intramolecular electron transfer converts Mn-III-citrate into Mn-II and citrate oxidation products. (c) 2006 Published by Elsevier Inc.

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