ABSTRACT
Two extraction reagents, hydrochloric acid (HCl) and acid ammonium oxalate solution (Tamm's reagent), were used to evaluate the redox state of iron in municipal solid waste (MSW) with different deposit ages. Orthogonal experiments were conducted to optimize the extraction conditions for extractable iron speciation (ferric and ferrous) in MSW. The optimal extraction conditions for HCl were determined as follows: the liquid-to-solid ratio was set at 100, and then the samples were extracted at the shaking speed of 200 rpm at 35 degrees C for 60 min by 1.00 M HCl. For Tamm's reagent, the optimal extraction conditions were extracted at the shaking speed of 175 rpm at 30 degrees C for 12 h with the same liquid-to-solid ratio. However, Tamm's reagent extraction is much more laborious and time-consuming. Thus the HC1 extraction might be a better choice for the evaluation of the redox state of iron in MSW. The results also showed that the yield of extractable iron increased with deposited age. About 60-83% of extractable iron was presented as ferrous in the MSW deposited for 1-8 years. This study supplied a tool for investigating the role of iron on the fate of pollutants in the landfill.
Subject(s)
Ferrous Compounds/isolation & purification , Refuse Disposal , Ferrous Compounds/classification , Hydrochloric Acid/chemistry , Oxidation-ReductionABSTRACT
El uso del Fumarato Ferroso Microencapsulado, produce una reducción significativa de la prevalencia de anemia en una población pediatrica de alto riesgo por presentar mejor adherencia a este. La aplicación de la nueva intervención en los Programas de Salud, aumentaria e n un 33 porciento los beneficio obtenidos por el nuevo suplemento, es decir que cada 3 niños tratados con Fumarato Ferroso, uno aumentará sus niveles de hemoglobina hasta alcanzar el estado no anémico...
Subject(s)
Tissue Adhesions/classification , Anemia/classification , Ferrous Compounds/classification , Fumarates/classificationABSTRACT
The phase and electrochemical behavior of the aqueous mixtures of monoolein (MO) and synthetic ferrocene (Fc) derivatives containing long alkyl chains-(Z)-octadec-9-enoylferrocene (1), (Z)-octadecen-9-ylferrocene (2), and ferrocenylmethyl (Z)-octadec-9-enoate (3)-were studied. At low hydration, the reversed micelles (L(2) phase) and cubic Q(230) phase of MO can accommodate relatively high amounts (>6 wt.%) of the Fc-derivative 2, whereas at high hydration, the pseudoternary cubic phase Q(224) is destabilized even at about 2 wt.% of this Fc. Increasing the Fc-derivative content induces L(alpha)-->L(2) and L(alpha)-->reversed bicontinuous cubic phase (Q(II))-->H(II) transitions depending upon hydration. A rough study of the MO system containing compounds 1 and 3 indicates very similar phase behavior to that of the MO/2/H(2)O system. Compound 2 apparently has no effect on the lipid monolayer thickness in the pseudoternary L(alpha), H(II) and Q(II) liquid crystalline phases of MO. Within a 3D-structure of the Q(224) phase, derivatives 1-3 exhibit electrochemical activity on the gold electrode. The one-electron redox conversion processes are electrochemically quasi-reversible and controlled by diffusion. The values of apparent diffusion coefficient (D(app)) and heterogeneous electron-transfer rate constant (k(s)) of Fcs are significantly lower in the cubic phase matrix when compared to the acetonitrile solution. By contrast, the MO H(II) phase with entrapped Fc-derivatives does not exhibit electrochemical activity on the electrode surface. It is suggested that the diffusional anisotropy and/or localized aggregation of compounds 1-3 within a 2D-structure of the H(II) phase account(s) for the latter observation.
