Boron incorporation into precipitated calcium carbonates affected by aqueous pH and boron concentration

JOURNAL OF HAZARDOUS MATERIALS

卷:383

Article

Kobayashi, Kazuki¹  Hashimoto, Yohey¹  Wang, Shan-Li² 

[1] Tokyo Univ Agr & Technol, Dept Bioapplicat & Syst Engn, 2-24-16 Koganei, Tokyo 1848588, Japan

[2] Natl Taiwan Univ, Dept Agr Chem, 1,Sect 4,Roosevelt Rd, Taipei 10617, Taiwan

关键词: Borate;    Boric acid;    Polyborate;    Coprecipitation;    X-ray absorption spectroscopy;   

DOI  :  10.1016/j.jhazmat.2019.121183

来源: Elsevier

【 摘 要 】

The objectives of this study were to investigate the amount of B incorporation into precipitated calcium carbonate (PCC) in the coprecipitation process, and to determine specific mineral phases (calcite or vaterite) and the mode of B coordination (trigonal or tetrahedral) in PCC under different pH and B concentrations. The amount of B incorporation into PCC increased in general with increasing aqueous B (B-aq) concentrations in the pH range from 8 to 12. The B removal by PCC reached maximum (similar to 200 mmol kg(-1)) at pH 10 with B-aq concentrations between 30 and 50 mM. The transformation of vaterite to calcite was promoted with increasing B-aq at pH 8 and 10, whereas an excess concentration of aqueous (poly)borate anions (100 mM) inhibited crystal growth of calcite. As determined by B K-edge X-ray absorption fine structure spectroscopy, the coordination of B incorporated in PCC was preferentially tetrahedral (B-IV, 55-70%) over trigonal (B-III, 30-45%) at B-aq < 75 mM. In contrast, the preferential incorporation of B-IV into PCC was not observed in the solution with a high B concentration (i.e., 100 mM). The amount of B incorporation, the morphology of PCC and B coordination in PCC were remarkably changed in high B-aq concentrations.

【 授权许可】

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