TY - JOUR
T1 - Control of aragonite formation and its crystal shape in CaCl2-Na2CO3-H2O reaction system
AU - Kogo, Mitsuaki
AU - Suzuki, Kenta
AU - Umegaki, Tetsuo
AU - Kojima, Yoshiyuki
N1 - Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/4/1
Y1 - 2021/4/1
N2 - Calcium carbonate (CaCO3) was synthesized in the CaCl2-Na2CO3-H2O reaction system at the reaction temperature of 40, 50, 60, and 70℃. The initial pH was changed to 2.4–11.0 at 50–70 ℃. The initial pH was adjusted by changing the pH of CaCl2 aqueous solution using HCl and NH3 aqueous solution. The CaCO3 precipitates obtained were characterized using X-ray diffraction (XRD), scanning electron microscope (SEM), and specific surface area measurement. In the case of no adding the pH adjustment solution, the product was a mixture of calcite and vaterite at 40 ℃. The formation of aragonite was observed at ≥50 ℃, and single-phase aragonite was obtained at ≥60 ℃, according to XRD measurements. Thus, Aragonite could be synthesized by changing the reaction temperature. At 70 ℃, the synthesis of CaCO3 was performed by changing the initial pH of 2.4–11.0. The formation of single-phase aragonite was detected in the initial pH range of 2.4–10.4. However, a small amount of calcite was contained in aragonite at the initial pH ≥ 10.8. The crystal shape of obtained aragonite was needle-like, and its particle size became finer as the initial pH increased. At an initial pH 2.4, the length and width of the crystals were 2–7 μm and 0.5–1.0 μm, respectively. The finest particles were samples synthesized at the initial pH 11.0, its length and width were 1–2 μm and 0.1–0.2 μm, respectively. The specific surface area of the products was 4.12–14.88 m2 g−1 at the initial pH of 2.4–11.0. The particle size of aragonite could be controlled by changing the initial pH at 70 ℃.
AB - Calcium carbonate (CaCO3) was synthesized in the CaCl2-Na2CO3-H2O reaction system at the reaction temperature of 40, 50, 60, and 70℃. The initial pH was changed to 2.4–11.0 at 50–70 ℃. The initial pH was adjusted by changing the pH of CaCl2 aqueous solution using HCl and NH3 aqueous solution. The CaCO3 precipitates obtained were characterized using X-ray diffraction (XRD), scanning electron microscope (SEM), and specific surface area measurement. In the case of no adding the pH adjustment solution, the product was a mixture of calcite and vaterite at 40 ℃. The formation of aragonite was observed at ≥50 ℃, and single-phase aragonite was obtained at ≥60 ℃, according to XRD measurements. Thus, Aragonite could be synthesized by changing the reaction temperature. At 70 ℃, the synthesis of CaCO3 was performed by changing the initial pH of 2.4–11.0. The formation of single-phase aragonite was detected in the initial pH range of 2.4–10.4. However, a small amount of calcite was contained in aragonite at the initial pH ≥ 10.8. The crystal shape of obtained aragonite was needle-like, and its particle size became finer as the initial pH increased. At an initial pH 2.4, the length and width of the crystals were 2–7 μm and 0.5–1.0 μm, respectively. The finest particles were samples synthesized at the initial pH 11.0, its length and width were 1–2 μm and 0.1–0.2 μm, respectively. The specific surface area of the products was 4.12–14.88 m2 g−1 at the initial pH of 2.4–11.0. The particle size of aragonite could be controlled by changing the initial pH at 70 ℃.
KW - A1. Characterization
KW - A1. Crystal morphology
KW - A1. Crystal structure
KW - A1. Morphological stability
KW - B1. Calcium compounds
UR - http://www.scopus.com/inward/record.url?scp=85100442042&partnerID=8YFLogxK
U2 - 10.1016/j.jcrysgro.2020.125964
DO - 10.1016/j.jcrysgro.2020.125964
M3 - Article
AN - SCOPUS:85100442042
SN - 0022-0248
VL - 559
JO - Journal of Crystal Growth
JF - Journal of Crystal Growth
M1 - 125964
ER -