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Polyphosphates and fulvates enhanve environmental stability of PO4-bearing colloidal iron oxyhydroxides

机译:多磷酸盐和富草酸酯增强了含PO4的胶态羟基氧化铁的环境稳定性

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摘要

Iron oxyhydroxide nanoparticles (Fe-NPs) are natural vectors of phosphate (PO4) in the environment. Their mobility is determined by colloidal stability, which is affected by surface composition. This might be manipulated in engineered NPs for environmental or agricultural applications. Here, the stability of PO4-Fe-NPs (HFO/goethite) was determined across contrasting environmental conditions (pH, Ca concentration) and by using fulvates (FA) and polyphosphates (poly-P’s) as coatings. The PO4-Fe-NPs are unstable at Ca concentrations above 0.1 mM. Addition of FA and some poly-P’s significantly improved stability. Zeta potential explained colloidal stability across treatments; surface charge was calculated with surface complexation models and explained for phytic acid (PA) and hexametaphosphate (HMP) by a partial (1–4 of the 6 PO4 units) adsorption to the surface, while the remaining PO4 units stayed in solution. This study suggests that Ca concentration mainly affects the mobility of natural or engineered PO4-Fe-NPs and that HMP is a promising agent for increasing colloidal stability.
机译:羟基氧化铁纳米颗粒(Fe-NPs)是环境中磷酸盐(PO4)的天然载体。它们的迁移率由胶体稳定性决定,胶体稳定性受表面组成的影响。在环境或农业应用的工程NP中可以对其进行操作。在这里,PO4-Fe-NPs(HFO /针铁矿)的稳定性是在不同的环境条件下(pH,Ca浓度)以及通过使用富铝酸盐(FA)和多磷酸盐(poly-P’s)进行涂层确定的。当Ca浓度超过0.1 mM时,PO4-Fe-NPs不稳定。添加FA和某些poly-P可以显着提高稳定性。 Zeta电位解释了整个处理过程中的胶体稳定性。用表面络合模型计算表面电荷,并通过部分(6个PO4单元中的1-4个)吸附到表面上来解释植酸(PA)和六偏磷酸盐(HMP),而其余PO4单元保留在溶液中。这项研究表明,钙的浓度主要影响天然或工程PO4-Fe-NPs的迁移率,而HMP是增加胶体稳定性的有前途的药物。

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