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91.
Walther Klüpfel 《International Journal of Earth Sciences》1956,45(2):318-327
Ohne ZusammenfassungVortrag, gehalten am 14. März 1955 auf der Hauptversammlung der Geologischen Vereinigung in Mainz. 相似文献
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The solubility of calcite in NaCl-H2O and in HCl-H2O fluids was measured using an extraction-quench hydrothermal apparatus. Experiments were conducted at 2 kbar, between 400° C and 600° C. Measurements in NaCl-H2O were conducted in two ways: 1) at constant pressure and NaCl concentration, as a function of temperature; and 2) at constant pressure and temperature, as a function of NaCl concentration. In both the NaCl-H2O and the HCl-H2O systems, the solubility of calcite increases with increasing chlorine concentrations. For example, the log calcium molality in equilibrium with calcite increases from –3.75 at 2 kbar and 500° C, in pure H2O to –3.10 at 2 kbar and 500° C at log NaCl molality=–1.67. At fixed pressure and NaCl molality, the solubility of calcite is almost constant from 400° C to 550° C, but increases somewhat at higher temperatures. The results can be used to determine the dominant calcium species in the experimental solutions as a function of NaCl concentration and to obtain values for the second dissociation constant of CaCl2(aq). At 2 kbar, 400° C, 500° C, and 600° C, we calculate values for the log of the dissociation constant of CaCl+ of –2.1, –3.2, and –4.3, respectively. The 400° C and 500° C values are consistent with those obtained by Frantz and Marshall (1982) using electrical conductance techniques. However, our 600° C value is 0.8 log units higher than that reported by Frantz and Marshall. The calcite solubilities in the NaCl-H2O and HCl-H2O systems are inconsistent with the solubilities of calcite in pure H2O reported by Walther and Long (1986). They are, however, consistent with the measurements of calcite solubilities in pure H2O presented in this study. These results allow for the calculation of the solubilities of calcium silicates and carbonates in fluids that contain CO2 and NaCl. 相似文献
94.
H.-J. Walther 《洁净——土壤、空气、水》1989,17(4):489-489
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H.-J. Walther 《洁净——土壤、空气、水》1985,13(5):582-582
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Rate and mechanism in prograde metamorphism 总被引:5,自引:3,他引:5
For a given rate of heat input into a prograde metamorphic sequence the extent of overstep of reaction temperature (disequilibrium) depends on the slowest of three sequential steps: (a) surface detachment of reactant minerals, (b) transport of material to the site of mineral growth, and (c) nucleation and growth of the product mineral. We have developed analytical expressions which enable determination of the rates of mineral dissolution and growth and of advective and diffusive mass transport during metamorphism. The dissolution and growth steps are linear functions of the driving force (– G) of the overall reaction while diffusion may take place either through a grain boundary fluid film or through the disorganized grain boundary itself.While little is known about heterogeneous nucleation, we argue from field observations that the rate of nucleation is not in general rate limiting. Additionally, if a fluid phase is present true grain boundary diffusion cannot be the mechanism which transports material over the mm to cm distances observed between reactant and product minerals.Simple models of contact (200° C temperature rise in 10,000 years) and regional (10° C per million years) metamorphic events lead to several conclusions concerning the rate determining step. Firstly, growth and dissolution are extremely rapid, dehydration reactions at 500° C going to completion in 2×102 years (contact) and 1×104 years (regional), if all solutes are readily transported. Secondly, the effect of substantial fracture flow of fluid is to divert the transporting medium away from the grain boundary region and hence to retard the transport step. Under most such circumstances it appears that diffusive transport of aqueous SiO2 or Mg species will be rate controlling. Despite this retardation of reaction rates, the extent of disequilibrium is rarely more than a few degrees C. Extensive disequilibrium (40° C) can only occur for reactions such as the andalusite sillimanite transformation which have very small entropy changes and which occur in rapid metamorphic events. 相似文献
100.
Andi Walther Marc Schröder Jürgen Fischer Ralf Bennartz 《Theoretical and Applied Climatology》2014,118(4):627-640
Observational data and simulations of the regional climate system Baltic integrated model system (BALTIMOS) were used to study precipitation in the Baltic Sea and its drainage basin with a special focus on the diurnal cycle. The study includes a general evaluation of BALTIMOS precipitation, showing that BALTIMOS has too many light rain events causing an overestimation of the total annual precipitation amount. The diurnal cycle as well as its spatial distribution was analysed. BALTIMOS captures the broad characteristics: a significant diurnal variability with an afternoon peak above land and weak variability with a nocturnal peak above sea. An algorithm to distinguish between frontal and convective precipitation was applied to examine the diurnal cycle more thoroughly. The local solar time of maximum rain in summer is about 1 to 2 h earlier in BALTIMOS than in radar observations of precipitation. 相似文献