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Phosphate adsorption on uncoated and humic acid-coated iron oxides

文献类型： 外文期刊

作者： Wang, Hui 1 ; Zhu, Jun 1 ; Fu, Qingling 1 ; Hong, Can 1 ; Hu, Hongqing 1 ; Violante, Antonio 3 ;

作者机构： 1.Huazhong Agr Univ, Coll Resources & Environm, Key Lab Arable Land Conservat Middle & Lower Reac, Minist Agr, Wuhan 430070, Peoples R China

2.Anhui Acad Agr Sci, Soil & Fertilizer Res Inst, Hefei 230031, Peoples R China

3.Univ Naples Federico II, Dept Soil Plant Environm & Anim Prod Sci, Fac Agr, Via Univ 100, I-80055 Portici Naples, Italy

关键词： Phosphate adsorption;Goethite;Hematite;In situ ATR-FTIR spectroscopy;Surface complexation;Zeta potential

期刊名称：JOURNAL OF SOILS AND SEDIMENTS （ 影响因子：3.308； 五年影响因子：3.586 ）

ISSN： 1439-0108

年卷期： 2016 年 16 卷 7 期

页码：

收录情况： SCI

摘要： Purpose The phosphate adsorption on natural adsorbents is of particular importance in regulating the transport and bioavailability of phosphates in environmental system. In soils, oxides are often associated with organic matter and form mineral-organic complexes. The aim of the present paper was to investigate the mechanisms of phosphate adsorption on these complexes. Materials and methods Phosphate adsorption on uncoated and humic acid (HA)-coated iron oxide complexes was investigated at different ionic strengths and pH by isotherm experiments and attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy. Results and discussion Results showed that HA-coated iron oxide complexes caused a decrease in the specific surface area (SSA) and the isoelectric point (IEP) of oxides. Phosphate adsorption on iron oxides was insensitive to changes of ionic strength, while it increased on the complexes with increasing ionic strength. The presence of HA decreased the maximum adsorption and the affinity of phosphate on the complexes. The zeta potential of phosphate-bound iron oxides linearly reduced with the increment of phosphate surface coverage, while the zeta potential of complexes with adsorbed phosphate kept at the same level. ATR-FTIR analysis suggested the formation of phosphate-metal complexation. The presence of HA promotes the formation of the monodentate phosphate complexes at pH 4.5 and significantly influenced phosphate species at pH 8.5. Conclusions The amount of phosphate adsorbed was reduced, and the phosphate speciation was also influenced when phosphate was adsorbed on HA-coated iron oxide complexes compared with phosphate adsorption on pure goethite and hematite.

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