Visualizing Organophosphate Precipitation at the Calcite-Water Interface by in Situ Atomic-Force Microscopy

Esters of phosphoric acid constitute a large fraction of the total organic phosphorus (OP) in the soil environment and, thus, play an important role in the global phosphorus cycle. These esters, such as glucose-6-phosphate (G6P), exhibit unusual reactivity toward various mineral particles in soils,...

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Main Authors: Wang, L., Qin, L., Putnis, C., Ruiz-Agudo, E., King, H., Putnis, Andrew
Format: Journal Article
Published: 2016
Online Access:http://hdl.handle.net/20.500.11937/38968
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author Wang, L.
Qin, L.
Putnis, C.
Ruiz-Agudo, E.
King, H.
Putnis, Andrew
author_facet Wang, L.
Qin, L.
Putnis, C.
Ruiz-Agudo, E.
King, H.
Putnis, Andrew
author_sort Wang, L.
building Curtin Institutional Repository
collection Online Access
description Esters of phosphoric acid constitute a large fraction of the total organic phosphorus (OP) in the soil environment and, thus, play an important role in the global phosphorus cycle. These esters, such as glucose-6-phosphate (G6P), exhibit unusual reactivity toward various mineral particles in soils, especially those containing calcite. Many important processes of OP transformation, including adsorption, hydrolysis, and precipitation, occur primarily at mineral–fluid interfaces, which ultimately governs the fate of organophosphates in the environment. However, little is known about the kinetics of specific mineral-surface-induced adsorption and precipitation of organophosphates. Here, by using in situ atomic-force microscopy (AFM) to visualize the dissolution of calcite (1014) faces, we show that the presence of G6P results in morphology changes of etch pits from the typical rhombohedral to a fan-shaped form. This can be explained by a site-selective mechanism of G6P–calcite surface interactions that stabilize the energetically unfavorable (0001) or (0112) faces through step-specific adsorption of G6P. Continuous dissolution at calcite (1014)–water interfaces caused a boundary layer at the calcite–water interface to become supersaturated with respect to a G6P–Ca phase that then drives the nucleation and growth of a G6P–Ca precipitate. Furthermore, after the introduction of the enzyme alkaline phosphatase (AP), the precipitates were observed to contain a mixture of components associated with G6P–Ca, amorphous calcium phosphate (ACP)–hydroxyapatite (HAP) and dicalcium phosphate dihydrate (DCPD). These direct dynamic observations of the transformation of adsorption- and complexation-surface precipitation and enzyme-mediated pathways may improve the mechanistic understanding of the mineral-interface-induced organophosphate sequestration in the soil environment.
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spelling curtin-20.500.11937-389682017-09-13T14:22:15Z Visualizing Organophosphate Precipitation at the Calcite-Water Interface by in Situ Atomic-Force Microscopy Wang, L. Qin, L. Putnis, C. Ruiz-Agudo, E. King, H. Putnis, Andrew Esters of phosphoric acid constitute a large fraction of the total organic phosphorus (OP) in the soil environment and, thus, play an important role in the global phosphorus cycle. These esters, such as glucose-6-phosphate (G6P), exhibit unusual reactivity toward various mineral particles in soils, especially those containing calcite. Many important processes of OP transformation, including adsorption, hydrolysis, and precipitation, occur primarily at mineral–fluid interfaces, which ultimately governs the fate of organophosphates in the environment. However, little is known about the kinetics of specific mineral-surface-induced adsorption and precipitation of organophosphates. Here, by using in situ atomic-force microscopy (AFM) to visualize the dissolution of calcite (1014) faces, we show that the presence of G6P results in morphology changes of etch pits from the typical rhombohedral to a fan-shaped form. This can be explained by a site-selective mechanism of G6P–calcite surface interactions that stabilize the energetically unfavorable (0001) or (0112) faces through step-specific adsorption of G6P. Continuous dissolution at calcite (1014)–water interfaces caused a boundary layer at the calcite–water interface to become supersaturated with respect to a G6P–Ca phase that then drives the nucleation and growth of a G6P–Ca precipitate. Furthermore, after the introduction of the enzyme alkaline phosphatase (AP), the precipitates were observed to contain a mixture of components associated with G6P–Ca, amorphous calcium phosphate (ACP)–hydroxyapatite (HAP) and dicalcium phosphate dihydrate (DCPD). These direct dynamic observations of the transformation of adsorption- and complexation-surface precipitation and enzyme-mediated pathways may improve the mechanistic understanding of the mineral-interface-induced organophosphate sequestration in the soil environment. 2016 Journal Article http://hdl.handle.net/20.500.11937/38968 10.1021/acs.est.5b05214 restricted
spellingShingle Wang, L.
Qin, L.
Putnis, C.
Ruiz-Agudo, E.
King, H.
Putnis, Andrew
Visualizing Organophosphate Precipitation at the Calcite-Water Interface by in Situ Atomic-Force Microscopy
title Visualizing Organophosphate Precipitation at the Calcite-Water Interface by in Situ Atomic-Force Microscopy
title_full Visualizing Organophosphate Precipitation at the Calcite-Water Interface by in Situ Atomic-Force Microscopy
title_fullStr Visualizing Organophosphate Precipitation at the Calcite-Water Interface by in Situ Atomic-Force Microscopy
title_full_unstemmed Visualizing Organophosphate Precipitation at the Calcite-Water Interface by in Situ Atomic-Force Microscopy
title_short Visualizing Organophosphate Precipitation at the Calcite-Water Interface by in Situ Atomic-Force Microscopy
title_sort visualizing organophosphate precipitation at the calcite-water interface by in situ atomic-force microscopy
url http://hdl.handle.net/20.500.11937/38968