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腐殖酸-铁共沉淀中磷的去除与结构发展的关系。

Phosphate Removal in Relation to Structural Development of Humic Acid-Iron Coprecipitates.

机构信息

Department of Soil and Environmental Sciences, National Chung Hsing University, 145 Xingda Rd., Taichung, 40227, Taiwan.

Scientific Research Division, National Synchrotron Radiation Research Center, 101 Hsin-Ann Rd., Hsinchu, 30043, Taiwan.

出版信息

Sci Rep. 2018 Jul 9;8(1):10363. doi: 10.1038/s41598-018-28568-7.

Abstract

Precipitation of Fe-hydroxide (FH) critically influences the sequestration of PO and organic matter (OM). While coatings of pre-sorbed OM block FH surfaces and decrease the PO adsorption capacity, little is known about how OM/Fe coprecipitation influences the PO adsorption. We aimed to determine the PO adsorption behaviors on humic acid (HA)-Fe coprecipitates in relation to surface and structural characteristics as affected by HA types and C/(C + Fe) ratios using the Fe and P X-ray absorption spectroscopy. With increasing C/(C + Fe) ratios, the indiscernible changes in the proportion of near-surface C for coprecipitates containing HA enriched in polar functional groups implied a relatively homogeneous distribution between C and Fe domains. Wherein PO adsorbed on FH dominated the P inventory on coprecipitates, yielding PO sorption properties nearly equivalent to that of pure FH. Structural disruptions of FH caused by highly associations with polar functional groups of HA enhanced the C solubilisation. While polar functional groups were limited, coprecipitates consisted of core FH with surface outgrowth of HA. Although surface-attached HA that was vulnerable to solubilisation provided alternatively sites for PO via ternary complex formation with Fe bridges, it also blocked FH surfaces, leading to a decrease in PO adsorption.

摘要

沉淀的 Fe 氢氧化物 (FH) 严重影响了 PO 和有机物 (OM) 的固定。虽然预吸附的 OM 涂层会阻碍 FH 表面,降低 PO 的吸附能力,但对于 OM/Fe 共沉淀如何影响 PO 的吸附知之甚少。我们旨在通过 Fe 和 P X 射线吸收光谱,确定与表面和结构特征相关的 HA-Fe 共沉淀上 PO 的吸附行为,这些特征受 HA 类型和 C/(C + Fe) 比的影响。随着 C/(C + Fe) 比的增加,富含极性官能团的 HA 共沉淀中近表面 C 的比例变化不大,表明 C 和 Fe 域之间存在相对均匀的分布。其中,在共沉淀上吸附的 PO 占据了 FH 上的 P 库存,导致 PO 吸附性能几乎与纯 FH 相当。HA 与 FH 强烈的极性官能团结合导致 FH 结构的破坏,增强了 C 的溶解。当极性官能团有限时,共沉淀由核心 FH 和表面生长的 HA 组成。虽然表面附着的 HA 容易溶解,通过与 Fe 桥的三元络合提供了替代的 PO 吸附位点,但它也会阻碍 FH 表面,导致 PO 吸附减少。

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