Polymorphism and morphology of calcium carbonate precipitated in mixed solvents of ethylene glycol and water

被引:112
作者
Flaten, Ellen Marie [1 ]
Seiersten, Marion [2 ]
Andreassen, Jens-Petter [1 ]
机构
[1] Norwegian Univ Sci & Technol, Dept Chem Engn, N-7491 Trondheim, Norway
[2] Inst Energy Technol, N-2027 Kjeller, Norway
关键词
Crystal morphology; Polymorphism; Growth from solutions; Calcium carbonate; FORMATION MECHANISM; VATERITE; GROWTH; ELECTROLYTES; AGGREGATION; PARTICLES;
D O I
10.1016/j.jcrysgro.2009.04.014
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The influence of (mono) ethylene glycol (MEG) on polymorphism and the resulting morphology of calcium carbonate have been Studied for activity-based supersaturation ratios in the range of 3-10 and temperatures from 25-80 degrees C in mixed solvents of ethylene glycol and water at ratios of 0-90 wt%. The presence of a co-solvent in the solution affects the supersaturation, because of changes in the activity coefficients and the solubility of the salt, a fact that is Usually not accounted for in similar studies in the literature. In the present study, the effect of the solvent was isolated from the accompanying change in the supersaturation. MEG was found to affect both the polymorphic abundance in the precipitates, the morphology of the particles and the transformation rates. High concentrations of MEG favoured the precipitation of vaterite and higher temperatures promoted the formation of aragonite. The particle size was reduced in experiments with high MEG concentrations at supersaturations ratios comparable to water solutions, illustrating that the nucleation rate is affected by the co-solvent. The morphology of the calcium carbonate particles was changed at various conditions of MEG concentrations and temperatures from cubes of calcite to spherical, flower-like and dumbbell particles of vaterite and aragonite needles. MEG prolongs the transformation time of metastable polymorphs and the effect was shown to be caused by the solvent itself, probably as a result of kinetic stabilization by delaying the growth rate of the more stable polymorphs. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:3533 / 3538
页数:6
相关论文
共 17 条
[1]   Formation mechanism and morphology in precipitation of vaterite - nano aggregation or crystal growth? [J].
Andreassen, JP .
JOURNAL OF CRYSTAL GROWTH, 2005, 274 (1-2) :256-264
[2]   Growth and aggregation of vaterite in seeded-batch experiments [J].
Andreassen, JP ;
Hounslow, MJ .
AICHE JOURNAL, 2004, 50 (11) :2772-2782
[3]   Switching between kinetic and thermodynamic control: calcium carbonate growth in the presence of a simple alcohol [J].
Dickinson, SR ;
McGrath, KM .
JOURNAL OF MATERIALS CHEMISTRY, 2003, 13 (04) :928-933
[4]   Quantitative determination of binary and tertiary calcium carbonate mixtures using powder X-ray diffraction [J].
Dickinson, SR ;
Mcgrath, KM .
ANALYST, 2001, 126 (07) :1118-1121
[5]  
DUGSTAD A, 2004, 87560 SPE
[6]   Morphology and formation mechanism of vaterite particles grown in glycine-containing aqueous solutions [J].
Hou, Wentao ;
Feng, Qingling .
MATERIALS SCIENCE & ENGINEERING C-BIOMIMETIC AND SUPRAMOLECULAR SYSTEMS, 2006, 26 (04) :644-647
[7]   Effect of anionic surfactant on vaterite CaCO3 [J].
Huang, J. H. ;
Mao, Z. F. ;
Luo, M. F. .
MATERIALS RESEARCH BULLETIN, 2007, 42 (12) :2184-2191
[8]  
KAASA B, 2004, 95075 SPE
[9]   Calcium carbonate phase analysis using XRD and FT-Raman spectroscopy [J].
Kontoyannis, CG ;
Vagenas, NV .
ANALYST, 2000, 125 (02) :251-255
[10]   Solvothermal growth of vaterite in the presence of ethylene glycol, 1,2-propanediol and glycerin [J].
Li, Q ;
Ding, Y ;
Li, FQ ;
Xie, B ;
Qian, YT .
JOURNAL OF CRYSTAL GROWTH, 2002, 236 (1-3) :357-362