Solution NMR investigation of phytic acid adsorption mechanisms at the calcite-water interface

被引:6
|
作者
Chen, Ai [1 ]
Zhu, Lingyang [2 ]
Arai, Yuji [1 ,3 ]
机构
[1] Univ Illinois, Dept Nat Resources & Environm Sci, Champaign, IL 61801 USA
[2] Univ Illinois, Sch Chem Sci, NMR Lab, Champaign, IL 61801 USA
[3] Environm Sci Univ Illinois Urbana Champaign, Dept Nat Resources, Champaign, IL 61801 USA
基金
美国食品与农业研究所;
关键词
Phytic acid; Adsorption; NMR; Calcite; pH; In situ; INOSITOL HEXAPHOSPHATE; PHOSPHATE SORPTION; AQUEOUS-SOLUTION; MYOINOSITOL HEXAPHOSPHATE; COLLOIDAL PHOSPHORUS; PHYTATE ION; METAL-IONS; P-31; NMR; SPECIATION; SOILS;
D O I
10.1016/j.scitotenv.2022.156700
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
As one of the most abundant organic phosphorus (P) species in soils, phytic acid could serve as a mineralizable P reservoir in soils and sediments. It has been widely acknowledged that the adsorption of phytic acid to soil minerals retards P mineralization in soils. However, the adsorption mechanisms of phytic acid in the minerals are not clearly understood. Using solution P-31 NMR and H-1 -P-31 2D NMR, the adsorption mechanism of phytic acid was investigated at the calcite-water interface at pH 6 and 8. Maximum phytic acid adsorption reached 3.07 mmol/g, 2.60 mmol/g, 2.39 mmol/g at pH 6, 8, and 9.5, respectively. The presence of outer-sphere surface complex was evident by a lack of significant change in zeta-potential of phytic acid reacted calcite. Solution NMR analysis showed a fast exchange process between adsorbed and unreacted phytic acid at the mineral surface on an NMR time scale, also indicating the outer-sphere complexation mechanism at both pH values. Interestingly, a more active role of P5 and P4,6 in binding with calcite surface was observed at pH 6. Adsorbed phytic acid on the calcite surface should be labile and is not limiting P mineralization in the terrestrial environment.
引用
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页数:11
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