CARBON ISOTOPIC FRACTIONATION BETWEEN CO2 VAPOR, SILICATE AND CARBONATE MELTS - AN EXPERIMENTAL-STUDY TO 30 KBAR

被引:96
作者
MATTEY, DP
TAYLOR, WR
GREEN, DH
PILLINGER, CT
机构
[1] UNIV TASMANIA,DEPT GEOL,HOBART,TAS 7001,AUSTRALIA
[2] UNIV WESTERN AUSTRALIA,DEPT GEOL,NEDLANDS,WA 6009,AUSTRALIA
[3] OPEN UNIV,DEPT EARTH SCI,MILTON KEYNES MK7 6AA,BUCKS,ENGLAND
关键词
D O I
10.1007/BF01575626
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 carbon isotopic fractionation between CO2 vapour and sodamelilite (NaCaAlSi2O7) melt over a range of pressures and temperatures has been investigated using solid-media piston-cylinder high pressure apparatus. Ag2C2O4 was the source of CO2 and experimental oxygen fugacity was buffered at hematite-magnetite by the double capsule technique. The abundance and isotopic composition of carbon dissolved in sodamelilite (SM) glass were determined by stepped heating and the δ13C of coexisting vapour was determined directly by capsule piercing. CO2 solubility in SM displays a complex behavior with temperature. At pressures up to 10 kbars CO2 dissolves in SM to form carbonate ion complexes and the solubility data suggest slight negative temperature dependence. Above 20 kbars CO2 reacts with SM to form immiscible Na-rich silicate and Ca-rich carbonate melts and CO2 solubility in Na-enriched silicate melt rises with increasing temperature above the liquidus. Measured values for carbon isotopic fractionation between CO2 vapour and carbonate ions dissoived in sodamelilite melt at 1200°-1400° C and 5-30 kbars average 2.4±0.2‰, favouring13C enrichment in CO2 vapour. The results are maxima and are independent of pressure and temperature. Similar values of ≈2‰ are obtained for the carbon isotopic fractionation between CO2 vapour and carbonate melts at 1300°-1400° C and 20-30 kbars. © 1990 Springer-Verlag.
引用
收藏
页码:492 / 505
页数:14
相关论文
共 36 条
[1]  
ALDER HH, 1963, AM MINERAL, V48, P839
[2]   CALCULATED FRACTIONATION FACTORS FOR CARBON AND HYDROGEN ISOTOPE EXCHANGE IN SYSTEM CALCITE-CARBON DIOXIDE-GRAPHITE-METHANE-HYDROGEN-WATER VAPOR [J].
BOTTINGA, Y .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1969, 33 (01) :49-&
[3]   APPARATUS FOR PHASE-EQUILIBRIUM MEASUREMENTS AT PRESSURES UP TO 50-KILOBARS AND TEMPERATURES UP TO 1750-DEGREES-C [J].
BOYD, FR ;
ENGLAND, JL .
JOURNAL OF GEOPHYSICAL RESEARCH, 1960, 65 (02) :741-748
[4]   CO2 SOLUBILITY AND SOLUBILITY MECHANISMS IN SILICATE MELTS AT HIGH-PRESSURES [J].
BREY, G .
CONTRIBUTIONS TO MINERALOGY AND PETROLOGY, 1976, 57 (02) :215-221
[5]   SOLUBILITY OF CO-2 IN OLIVINE MELILITITE AT HIGH-PRESSURES AND ROLE OF CO-2 IN EARTHS UPPER MANTLE [J].
BREY, GP ;
GREEN, DH .
CONTRIBUTIONS TO MINERALOGY AND PETROLOGY, 1976, 55 (02) :217-230
[6]   VOLATILES IN PILLOW RIM GLASSES FROM LOIHI AND KILAUEA VOLCANOS, HAWAII [J].
BYERS, CD ;
GARCIA, MO ;
MUENOW, DW .
GEOCHIMICA ET COSMOCHIMICA ACTA, 1985, 49 (09) :1887-1896
[8]   CARBON AND ITS ISOTOPES IN MID-OCEANIC BASALTIC GLASSES [J].
DESMARAIS, DJ ;
MOORE, JG .
EARTH AND PLANETARY SCIENCE LETTERS, 1984, 69 (01) :43-57
[9]  
DIENES P, 1986, 4TH INT KIMB C GEOL, V16, P383
[10]   CARBON-DIOXIDE IN SILICATE MELTS .2. SOLUBILITIES OF CO2 AND H2O IN CAMGSI2O6 (DIOPSIDE) LIQUIDS AND VAPORS AT PRESSURES TO 40 KB [J].
EGGLER, DH ;
ROSENHAUER, M .
AMERICAN JOURNAL OF SCIENCE, 1978, 278 (01) :64-94