TY - JOUR
T1 - Oxygen isotope fractionation factors between anhydrite and water from 100 to 550°C
AU - Chiba, Hitoshi
AU - Kusakabe, Minoru
AU - Hirano, Shin Ichi
AU - Matsuo, Sadao
AU - Somiya, Shigeyuki
N1 - Funding Information:
This work was supported in part by grant in aid for scientific research No. 254180 (M.K.), from the Ministry of Education, Science and Culture, Japan.
PY - 1981/3
Y1 - 1981/3
N2 - Oxygen isotope exchange between anhydrite and water was studied from 100 to 550°C, using the partial equilibrium method. The exchange rate was extremely low in NaCl solution. In the lower-temperature range, acid solutions were used to produce sufficient reaction to determine the oxygen isotope fractionation factors. The fractionation factors obtained in the present study are definitely different from those given by Lloyd [8]. They are similar to those for the HSO4--water system studied by Mizutani and Rafter [19], and are consistently 2‰ higher than those of the barite-water system by Kusakabe and Robinson [5]. The temperature dependence of the oxygen isotope fractionation factors was calculated by the least squares method in which the weight was taken to be inversely proportional to the experimental error. The fractionation is given by:103lnαanhydrite-water=3.21×(103/T)2-4.72. Available δ18O values of natural anhydrite were used to test the validity of this expression. It is shown that this newly revised geothermometer can be successfully applied to natural hydrothermal anhydrite.
AB - Oxygen isotope exchange between anhydrite and water was studied from 100 to 550°C, using the partial equilibrium method. The exchange rate was extremely low in NaCl solution. In the lower-temperature range, acid solutions were used to produce sufficient reaction to determine the oxygen isotope fractionation factors. The fractionation factors obtained in the present study are definitely different from those given by Lloyd [8]. They are similar to those for the HSO4--water system studied by Mizutani and Rafter [19], and are consistently 2‰ higher than those of the barite-water system by Kusakabe and Robinson [5]. The temperature dependence of the oxygen isotope fractionation factors was calculated by the least squares method in which the weight was taken to be inversely proportional to the experimental error. The fractionation is given by:103lnαanhydrite-water=3.21×(103/T)2-4.72. Available δ18O values of natural anhydrite were used to test the validity of this expression. It is shown that this newly revised geothermometer can be successfully applied to natural hydrothermal anhydrite.
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U2 - 10.1016/0012-821X(81)90025-X
DO - 10.1016/0012-821X(81)90025-X
M3 - Article
AN - SCOPUS:0009786564
SN - 0012-821X
VL - 53
SP - 55
EP - 62
JO - Earth and Planetary Sciences Letters
JF - Earth and Planetary Sciences Letters
IS - 1
ER -