Jm. Rosenbaum, STABLE-ISOTOPE FRACTIONATION BETWEEN CARBON-DIOXIDE AND CALCITE AT 900-DEGREES-C, Geochimica et cosmochimica acta, 58(17), 1994, pp. 3747-3753
Equilibrium stable isotope fractionation factors between carbon dioxid
e and calcite were determined by direct equilibration of the two phase
s at 900 degrees C and 12.5 kbar. The results of six three-day runs ga
ve Delta(13)C(CO2-calcite) and Delta(18)O(CO2-calcite) fractionations
of +2.70 +/- 0.36 parts per thousand and +3.30 +/- 0.16 parts per thou
sand, respectively (2 sigma). Runs of 22.5, 45, and 90 min; and 3, 6,
12, and 24 h duration were also conducted. Rapid initial recrystalliza
tion accompanied by extensive carbon and oxygen isotope exchange (grea
ter than or similar to 40%) and a very high oxygen/carbon exchange rat
e ratio (similar to 5) was seen in runs using both natural and synthet
ic calcite. Subsequent exchange slowed drastically, and the rate of ox
ygen exchange decreased relative to that of carbon to a constant value
of similar to 3, implicating the involvement of carbonate ion migrati
on in the later, slower stages of exchange. The lower limits of bulk c
arbon and oxygen diffusion coefficients determined from the partial ex
change experiments were 4 X 10(-13) and 9 x 10(-13) (cm(2)/s), respect
ively.