The normal grain growth behaviour of nominally pure calcitic aggregates

被引:58
作者
CoveyCrump, SJ
机构
[1] Rock and Ice Physics Laboratory, Department of Geological Sciences, University College London, London WC1E 6BT, Gower Street
关键词
D O I
10.1007/s004100050335
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
The normal grain growth behaviour of four different, but all nominally pure, calcite powders (99%+ analytic grade calcite, 99.7% chalk, 99.97% crushed Iceland Spar, 99.95% + chelometric grade calcite) has been investigated as a function of temperature (550, 600, 650, 700 degrees C) and confining pressure (100, 190 MPa) under both ''dry'' and hydrostatic (P-fluid = P-total) conditions. The initial particle size of both the analytic grade and chelometric grade calcite was about 5 mu m, and that of the chalk was about 3 mu m, while the experiments on the Iceland Spar were conducted on powders of three different initial particle sizes (3.4, 7.5, 38.5 mu m). On each material, at each pressure/temperature condition 6 to 15 experiments, equally spaced in log time from 15 minutes to 50 days, were conducted. Under dry conditions all four materials recrystallized to aggregates which contained less than 2% porosity and which had a grain size of between 4 and 20 Cum (depending on the initial particle size). Subsequently the aggregates coarsened by normal grain growth, with the kinetics of the growth process being controlled by the rate at which the grain boundaries could drag the residual pores with them as they migrated. Under nominally identical conditions both the mechanism and rates of pore drag differed greatly for the different materials, implying that this process is highly sensitive to trace solute impurity concentrations. This sensitivity renders the task of providing a systematic account of dry calcite grain growth kinetics highly problematic. Under hydrostatic conditions all the pow powders followed the same normal grain growth kinetics in which the growth process was rate-controlled by diffusion through the pore fluid on the grain boundaries. An activation enthalpy of 162.6 kJ mol(-1) and an activation volume of 34.35 cm(3) mol(-1) was obtained for this process.
引用
收藏
页码:239 / 254
页数:16
相关论文
共 38 条
[1]   A THEORY OF TEXTURE CONTROLLED GRAIN-GROWTH .1. DERIVATION AND GENERAL DISCUSSION OF THE MODEL [J].
ABBRUZZESE, G ;
LUCKE, K .
ACTA METALLURGICA, 1986, 34 (05) :905-914
[2]  
Aboav D. A., 1972, Metallography, V5, P251, DOI 10.1016/0026-0800(72)90004-3
[3]  
Aboav D. A., 1971, Metallography, V4, P425, DOI 10.1016/0026-0800(71)90050-4
[4]   COMPUTER-SIMULATION OF NORMAL GRAIN-GROWTH IN 3 DIMENSIONS [J].
ANDERSON, MP ;
GREST, GS ;
SROLOVITZ, DJ .
PHILOSOPHICAL MAGAZINE B-PHYSICS OF CONDENSED MATTER STATISTICAL MECHANICS ELECTRONIC OPTICAL AND MAGNETIC PROPERTIES, 1989, 59 (03) :293-329
[5]   GRAIN GROWTH IN METALS OF CLOSE-PACKED HEXAGONAL STRUCTURE [J].
ANDRADE, END ;
ABOAV, DA .
PROCEEDINGS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL AND PHYSICAL SCIENCES, 1966, 291 (1424) :18-&
[6]  
[Anonymous], 1976, CERAMIC MICROSTRUCTU
[7]   THEORIES OF NORMAL GRAIN-GROWTH IN PURE SINGLE-PHASE SYSTEMS [J].
ATKINSON, HV .
ACTA METALLURGICA, 1988, 36 (03) :469-491
[8]   CRITICAL CONCENTRATION OF MGO FOR THE PREVENTION OF ABNORMAL GRAIN-GROWTH IN ALUMINA [J].
BAE, SI ;
BAIK, S .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1994, 77 (10) :2499-2504
[9]  
BECK PA, 1949, T AM I MIN MET ENG, V185, P240
[10]  
BLOOMFIELD JP, 1996, J HYDROL, V184, P335