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Influence of Complex Structure on the Biodegradation of Iron-Citrate Complexes

机译:配合物结构对柠檬酸铁配合物生物降解的影响

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摘要

The biodegradation of iron-citrate complexes depends on the structure of the complex formed between the metal and citric acid. Ferric iron formed a bidentate complex with citric acid, [Fe(III) (OH)2 cit]2- involving two carboxylic acid groups, and was degraded at the rate of 86 μM h-1. In contrast, ferrous iron formed a tridentate complex with citric acid, [Fe(II) cit]-, involving two carboxylic acid groups and the hydroxyl group, and was resistant to biodegradation. However, oxidation and hydrolysis of the ferrous iron resulted in the formation of a tridentate ferric-citrate complex, [Fe(III)OH cit]-, which was further hydrolyzed to a bidentate complex, [Fe(III)(OH)2 cit]2-, that was readily degraded. The rate of degradation of the ferrous-citrate complex depended on the rate of its conversion to the more hydrolyzed form of the ferric-citrate complex. Bacteria accelerated the conversion much more than did chemical oxidation and hydrolysis.
机译:柠檬酸铁络合物的生物降解取决于金属和柠檬酸之间形成的络合物的结构。三价铁与柠檬酸形成[[Fe(III)(OH)2 cit] 2-包含两个羧酸基团的双齿络合物,并以86μMh -的速率降解1 。相反,亚铁与柠檬酸[Fe(II)cit] -形成三齿复合物,涉及两个羧酸基和羟基,并且具有抗生物降解性。但是,二价铁的氧化和水解导致形成三齿柠檬酸三铁络合物[Fe(III)OH cit] -,然后进一步水解为二齿络合物[Fe( III)(OH)2 cit] 2-,很容易降解。柠檬酸亚铁络合物的降解速率取决于其转化为柠檬酸铁络合物的更水解形式的速率。细菌比化学氧化和水解更能促进转化。

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