Grain growth kinetics of dolomite, magnesite and calcite: a comparative study

被引:22
作者
Davis, N. E. [1 ]
Newman, J. [1 ]
Wheelock, P. B. [2 ]
Kronenberg, A. K. [1 ]
机构
[1] Texas A&M Univ, Ctr Tectonophys, Dept Geol & Geophys, College Stn, TX 77843 USA
[2] Iowa State Univ, Mat Preparat Ctr, Ames Lab, Ames, IA 50011 USA
基金
美国国家科学基金会;
关键词
Grain growth; Kinetics; Pinning; Dolomite; Carbonates; HOT-PRESSED CALCITE; BOUNDARY DIFFUSION; 2ND-PHASE PARTICLES; DYNAMIC RECRYSTALLIZATION; DISSOLVED MAGNESIUM; FAULT ZONE; DEFORMATION; OXYGEN; CREEP; SIZE;
D O I
10.1007/s00269-010-0389-9
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The rates of grain growth of stoichiometric dolomite [CaMg(CO3)(2)] and magnesite (MgCO3) have been measured at temperatures T of 700-800A degrees C at a confining pressure P (c) of 300 MPa, and compared with growth rates of calcite (CaCO3). Dry, fine-grained aggregates of the three carbonates were synthesized from high purity powders by hot isostatic pressing (HIP); initial mean grain sizes of HIP-synthesized carbonates were 1.4, 1.1, and 17 mu m, respectively, for CaMg(CO3)(2), MgCO3, and CaCO3, with porosities of 2, 28, and 0.04% by volume. Grain sizes of all carbonates coarsened during subsequent isostatic annealing, with mean values reaching 3.9, 5.1, and 27 mu m for CaMg(CO3)(2), MgCO3, and CaCO3, respectively, in 1 week. Grain growth of dolomite is much slower than the growth rates of magnesite or calcite; assuming normal grain growth and n = 3 for all three carbonates, the rate constant K for dolomite (a parts per thousand integral 5 x 10(-5) mu m(3)/s) at T = 800A degrees C is less than that for magnesite by a factor of similar to 30 and less than that for calcite by three orders of magnitude. Variations in carbonate grain growth may be affected by differences in cation composition and densities of pores at grain boundaries that decrease grain boundary mobility. However, rates of coarsening correlate best with the extent of solid solution; K is the largest for calcite with extensive Mg substitution for Ca, while K is the smallest for dolomite with negligible solid solution. Secondary phases may nucleate at advancing dolomite grain boundaries, with implications for deformation processes, rheology, and reaction kinetics of carbonates.
引用
收藏
页码:123 / 138
页数:16
相关论文
共 79 条
[1]   PHASE-EQUILIBRIA IN THE SYSTEM CACO3-MGCO3-FECO3 [J].
ANOVITZ, LM ;
ESSENE, EJ .
JOURNAL OF PETROLOGY, 1987, 28 (02) :389-414
[2]   Textural controls on the brittle deformation of dolomite: variations in peak strength [J].
Austin, N. J. ;
Kennedy, L. A. .
DEFORMATION MECHANISMS, RHEOLOGY AND TECTONICS: FROM MINERALS TO THE LITHOSPHERE, 2005, 243 :37-49
[3]   THE PLASTIC-DEFORMATION OF POLYCRYSTALLINE DOLOMITE - COMPARISON OF EXPERIMENTAL RESULTS WITH THEORETICAL PREDICTIONS [J].
BARBER, DJ ;
WENK, HR ;
HEARD, HC .
MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING, 1994, 175 (1-2) :83-104
[4]   P-T-X(CO2) CONDITIONS OF CONTACT-METAMORPHISM IN THE BLACK BUTTE AUREOLE, ELKHORN, MONTANA [J].
BOWMAN, JR ;
ESSENE, EJ .
AMERICAN JOURNAL OF SCIENCE, 1982, 282 (03) :311-340
[5]  
Brook R.J., 1976, TREATISE MAT SCI TEC, V9, P331
[6]   RECRYSTALLIZATION AND GRAIN GROWTH [J].
BURKE, JE ;
TURNBULL, D .
PROGRESS IN METAL PHYSICS, 1952, 3 :220-292
[7]   Effects of matrix grain size on the kinetics of intergranular diffusion [J].
Carlson, WD ;
Gordon, CL .
JOURNAL OF METAMORPHIC GEOLOGY, 2004, 22 (08) :733-742
[8]   ISOTOPIC EXCHANGE IN MINERAL-FLUID SYSTEMS .1. THEORETICAL EVALUATION OF OXYGEN ISOTOPIC EXCHANGE ACCOMPANYING SURFACE-REACTIONS AND DIFFUSION [J].
COLE, DR ;
OHMOTO, H ;
LASAGA, AC .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1983, 47 (10) :1681-1693
[9]   SINTERING OF OLIVINE AND OLIVINE-BASALT AGGREGATES [J].
COOPER, RF ;
KOHLSTEDT, DL .
PHYSICS AND CHEMISTRY OF MINERALS, 1984, 11 (01) :5-16
[10]   THERMALLY-INDUCED GRAIN-GROWTH OF CALCITE MARBLES ON NAXOS ISLAND, GREECE [J].
COVEYCRUMP, SJ ;
RUTTER, EH .
CONTRIBUTIONS TO MINERALOGY AND PETROLOGY, 1989, 101 (01) :69-86