Characterization of the intermediate in formation of selenate-substituted ettringite

Binglin Guo, Keiko Sasaki, Tsuyoshi Hirajima

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

Precipitation of SeO42 −-substituted ettringite is an efficient method to immobilize SeO42 − under alkaline conditions. The effect of SO42 − on SeO42 − immobilization was investigated, because SO42 − is one of the major ions in aqueous and soil environments and it is easily incorporated in ettringite. We aimed to systemically elucidate the formation mechanisms of SeO42 −-substituted ettringite with and without SO42 −. When SO42 − and SeO42 − coexisted, both oxoanions were immediately coprecipitated with ettringite after adding a Ca source. Although SO42 − was partially substituted by SeO42 − in ettringite, no other phases were formed during the process. Without SO42 −, SeO42 −-substituted AFm phase was formed as an intermediate, confirmed by X-ray diffraction peak at d 2.878, as well as by scanning electron microscopy with energy dispersive X-ray spectroscopy and zeta potential measurements. It is clear that the incorporation mechanism of SeO42 − in ettringite is dependent on coexisting SO42 − in aqueous environments.

Original languageEnglish
Pages (from-to)30-37
Number of pages8
JournalCement and Concrete Research
Volume99
DOIs
Publication statusPublished - Sep 1 2017

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Selenic Acid
Zeta potential
Soils
X ray diffraction
Scanning electron microscopy
Ions
X-Ray Emission Spectrometry
ettringite

All Science Journal Classification (ASJC) codes

  • Building and Construction
  • Materials Science(all)

Cite this

Characterization of the intermediate in formation of selenate-substituted ettringite. / Guo, Binglin; Sasaki, Keiko; Hirajima, Tsuyoshi.

In: Cement and Concrete Research, Vol. 99, 01.09.2017, p. 30-37.

Research output: Contribution to journalArticle

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abstract = "Precipitation of SeO42 −-substituted ettringite is an efficient method to immobilize SeO42 − under alkaline conditions. The effect of SO42 − on SeO42 − immobilization was investigated, because SO42 − is one of the major ions in aqueous and soil environments and it is easily incorporated in ettringite. We aimed to systemically elucidate the formation mechanisms of SeO42 −-substituted ettringite with and without SO42 −. When SO42 − and SeO42 − coexisted, both oxoanions were immediately coprecipitated with ettringite after adding a Ca source. Although SO42 − was partially substituted by SeO42 − in ettringite, no other phases were formed during the process. Without SO42 −, SeO42 −-substituted AFm phase was formed as an intermediate, confirmed by X-ray diffraction peak at d 2.878, as well as by scanning electron microscopy with energy dispersive X-ray spectroscopy and zeta potential measurements. It is clear that the incorporation mechanism of SeO42 − in ettringite is dependent on coexisting SO42 − in aqueous environments.",
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N2 - Precipitation of SeO42 −-substituted ettringite is an efficient method to immobilize SeO42 − under alkaline conditions. The effect of SO42 − on SeO42 − immobilization was investigated, because SO42 − is one of the major ions in aqueous and soil environments and it is easily incorporated in ettringite. We aimed to systemically elucidate the formation mechanisms of SeO42 −-substituted ettringite with and without SO42 −. When SO42 − and SeO42 − coexisted, both oxoanions were immediately coprecipitated with ettringite after adding a Ca source. Although SO42 − was partially substituted by SeO42 − in ettringite, no other phases were formed during the process. Without SO42 −, SeO42 −-substituted AFm phase was formed as an intermediate, confirmed by X-ray diffraction peak at d 2.878, as well as by scanning electron microscopy with energy dispersive X-ray spectroscopy and zeta potential measurements. It is clear that the incorporation mechanism of SeO42 − in ettringite is dependent on coexisting SO42 − in aqueous environments.

AB - Precipitation of SeO42 −-substituted ettringite is an efficient method to immobilize SeO42 − under alkaline conditions. The effect of SO42 − on SeO42 − immobilization was investigated, because SO42 − is one of the major ions in aqueous and soil environments and it is easily incorporated in ettringite. We aimed to systemically elucidate the formation mechanisms of SeO42 −-substituted ettringite with and without SO42 −. When SO42 − and SeO42 − coexisted, both oxoanions were immediately coprecipitated with ettringite after adding a Ca source. Although SO42 − was partially substituted by SeO42 − in ettringite, no other phases were formed during the process. Without SO42 −, SeO42 −-substituted AFm phase was formed as an intermediate, confirmed by X-ray diffraction peak at d 2.878, as well as by scanning electron microscopy with energy dispersive X-ray spectroscopy and zeta potential measurements. It is clear that the incorporation mechanism of SeO42 − in ettringite is dependent on coexisting SO42 − in aqueous environments.

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