Ca and Co substitutions in (Ca,Co)(OH)2 hydroxides

被引:2
|
作者
Delorme, F. [1 ]
Giovannelli, F. [1 ]
Autret-Lambert, C. [1 ]
Chartier, T. [1 ]
机构
[1] Univ Tours, GREMAN, CNRS, UMR 7347, F-41000 Blois, France
关键词
Inorganic compounds; Layered compounds; Chemical synthesis; Electron microscopy; X-ray diffraction; HYDROTALCITE-LIKE PHASES; COBALT HYDROXIDE; NICKEL HYDROXIDES; NEUTRON-DIFFRACTION; CRYSTAL-STRUCTURE; BRUCITE-LIKE; DOUBLE SALTS; BETA-CO(OH)(2); OXYHYDROXIDE; SPECTROSCOPY;
D O I
10.1016/j.materresbull.2013.06.073
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
According to DFT simulation, no mixed hydroxide containing calcium and a small divalent cation with the brucite structure is possible. This experimental study confirms that between portlandite (Ca(OH)(2)) and beta-Co(OH)(2), a solid solution does not exist. Samples have been synthesized by coprecipitation under flowing nitrogen at room temperature. However, XRD, TEM and DTA/TG analyses show that a partial solubility exists and that the substitution limit of calcium in beta-Co(OH)(2) is lower than 12% and lower than 7% for cobalt in Ca(OH)(2). The two kinds of particles exhibit similar plate-like morphology with a size between 50 and 200 nm and a thickness of about 10 nm. The origin of such low substitution limits could be the difference in radii between calcium and cobalt generating local stresses. Substitutions by small amounts of different cations to reduce the local stresses such as Al, Sr or Cu have failed to allow improving significantly the substitution limits. An alternative synthesis route consisting in contacting the first cation oxide in a solution containing a salt of the second cation has also failed to reach a complete solid solution between portlandite and beta-Co(OH)(2). (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4191 / 4195
页数:5
相关论文
共 50 条
  • [21] Inhibition mechanism of magnesium ion on carbonation reaction with Ca(OH)2 and CO2
    Kim, Jeong-Hwan
    Ahn, Ji-Whan
    Ko, Sang-Jin
    Park, Woon-Kyoung
    Han, Choon
    [J]. ECO-MATERIALS PROCESSING & DESIGN VII, 2006, 510-511 : 990 - 993
  • [22] CHEMICAL ABSORPTION OF CO2 AND SO2 INTO Ca(OH)2 SLURRY.
    Yagi, Hideharu
    Okamoto, Kyosuke
    Naka, Keiji
    Hikita, Haruo
    [J]. 1600, (26): : 1 - 3
  • [23] Influences of Bi and Cu substitutions on the power factor of Ca3CO2O6
    Iwasaki, K
    Yamane, H
    Takahashi, J
    Kubota, S
    Nagasaki, T
    Arita, Y
    Nishi, Y
    Matsui, T
    Shimada, M
    [J]. JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, 2005, 66 (2-4) : 303 - 307
  • [24] Properties and Microstructure of Na2CO3-Activated Binders Modified with Ca(OH)2 and Mg(OH)2
    Xie, Lilan
    Liu, Kaiwei
    [J]. MATERIALS, 2022, 15 (05)
  • [25] Highly Surface-Active Ca(OH)2 Monolayer as a CO2 Capture Material
    Ozcelik, V. Ongun
    Gong, Kai
    White, Claire E.
    [J]. NANO LETTERS, 2018, 18 (03) : 1786 - 1793
  • [26] Role of Aspartic Acid in the Synthesis of Spherical Vaterite by the Ca(OH)2-CO2 Reaction
    Luo, Jia
    Kong, Fantao
    Ma, Xinsheng
    [J]. CRYSTAL GROWTH & DESIGN, 2016, 16 (02) : 728 - 736
  • [27] Effects of temperature on conversion of Li2CO3 to LiOH in Ca(OH)2 suspension
    Yuan, Bo
    Wang, Jing
    Cai, Wei
    Yang, Yurong
    Yi, Meigui
    Xiang, Lan
    [J]. PARTICUOLOGY, 2017, 34 : 97 - 102
  • [28] Carbonation Kinetics of Ca(OH)2 Under Conditions of Entrained Reactors to Capture CO2
    Arias, B.
    Criado, Y. A.
    Paneda, B.
    Abanades, J. C.
    [J]. INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2022, 61 (09) : 3272 - 3277
  • [29] Computational design of defect-engineered Ca(OH)2 monolayer for CO2 capture
    Ozcelik, Ongun
    Gong, Kai
    White, Claire
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2018, 255
  • [30] In vitro efficiency of 16 different Ca(OH)2 based CO2 absorbent brands
    Yan Jiang
    Mohammed K. Bashraheel
    Hongliang Liu
    Jan Poelaert
    Marc Van de Velde
    Geert Vandenbroucke
    Rik Carette
    Andre M. De Wolf
    Jan F. A. Hendrickx
    [J]. Journal of Clinical Monitoring and Computing, 2019, 33 : 1081 - 1087