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R.O. Fournier

Publications and source records attributed to R.O. Fournier.

25 records · Page 2Linked to original sources

Geochemical indicators of subsurface temperature: Part 1, basic assumptions

The chemical and isotopic compositions of hot-spring water and gas are used to estimate subsurface temperatures. The basic assumptions inherent in the methods are seldom stipulated. These assumptions include (1) a temperature-dependent reaction at depth, (2) a supply of the solid phase involved in the reaction to permit saturation of the constituent used for geothermometry, (3) water-rock equilibrium at depth, (4) negligible re-equilibration as the water flows to the surface, and (5) no dilution or mixing of hot and cold water. The first three assumptions are probably good for a few reactions that occur in many places. The last two assumptions probably are not valid for many hot-spring systems; information obtained is therefore for the shallower parts of those systems, or a limiting temperature (generally a minimum) is indicated.

Journal of Research of the U.S. Geological Survey

Geochemical indicators of subsurface temperature: Part 2, estimation of temperature and fraction of hot water mixed with cold water

The water in many warm springs with large rates of flow consists of mixtures of hot water that has come from depth and of shallow cold water. Under favorable conditions the original temperature of the hot water and the fraction of the cold water in the mixture can be estimated by using the measured temperature and silica content of the warm spring water and the temperature and silica content of nonthermal water in the region. The method has been applied with apparent success at Yellowstone National Park.

Wyoming

An empirical NaKCa geothermometer for natural waters

An empirical method of estimating the last temperature of water-rock interaction has been devised. It is based upon molar Na, K and Ca concentrations in natural waters from temperature environments ranging from 4 to 340°C. The data for most geothermal waters cluster near a straight line when plotted as the function log ( Na K ) + β log [ √ (Ca) Na ] "> log (NaK) + β log [ √(Ca)Na] vs reciprocal of absolute temperature, where β is either 1 3 "> 13 or 4 3 "> 43 depending upon whether the water equilibrated above or below 100°C. For most waters tested, the method gives better results than the Na K "> NaK methods suggested by other workers. The ratio Na K "> NaK should not be used to estimate temperature if √ ( M Ca ) M Na "> √ (MCa)MNa is greater than 1. The Na K "> NaK values of such waters generally yield calculated temperatures much higher than the actual temperature at which water interacted with the rock. A comparison of the composition of boiling hot-spring water with that obtained from a nearby well (170°C) in Yellowstone Park shows that continued water-rock reactions may occur during ascent of water even though that ascent is so rapid that little or no heat is lost to the country rock, i.e. the water cools adiabatically. As a result of such continued reaction, waters which dissolve additional Ca as they ascend from the aquifer to the surface will yield estimated aquifer temperatures that are too low. On the other hand, waters initially having enough Ca to deposit calcium carbonate during ascent may yield estimated aquifer temperatures that are too high if aqueous Na and K are prevented from further reaction with country rock owing to armoring by calcite or silica minerals. The Na-K-Ca geothermometer is of particular interest to those prospecting for geothermal energy. The method also may be of use in interpreting compositions of fluid inclusions.

Wyoming

More on noble gases in Yellowstone National Park hot waters

Water and gas samples from research wells in hydrothermal areas of Yellowstone National Park, U.S.A., have been mass spectrometrically analyzed for their rare gas contents and isotopic composition. In agreement with previous findings, the rare gases have been found to originate from infiltrating run-off water, saturated with air at 10 to 20°C. The atmospheric rare gas retention values found for the water varied between 3 and 87 per cent. The fine structure of the Ar, Kr and Xe abundance pattern in the water reveals fraotionational enrichment of the heavier gases due to partial outgassing of the waters. Radiogenic He and Ar have been detected. No positive evidence for magmatic water contribution has been found. Nevertheless, additions of magmatic waters free of rare gas can not be excluded, but if present the proportion is significantly less than 13 to 36 per cent.

Wyoming

The system K2Mg2(SO4)3 (langbeinite)-K2Ca2(SO4)3 (calcium-langbeinite)

The join between the compositions K 2 Mg 2 (SO 4 ) 3 and K 2 Ca 2 (SO 4 ) 3 was studied by means of high-temperature equilibrium quenching techniques and by means of a heating stage mounted on an X-ray diffractometer. Complete solid solution exists in the system, but at 25°C members of the solid solution series are isometric only in the composition range 0–73·5 wt. per cent K 2 Ca 2 (SO 4 ) 3 . At compositions richer in K 2 Ca 2 (SO 4 ) 3 than 73·5 wt. per cent, members of the series are optically biaxial. At higher temperatures members of the solid solution series are isometric at successively more calcium-rich compositions and pure K 2 Ca 2 (SO 4 ) 3 is isometric above about 200 ± 2°C. The system is not binary, as mixtures richer in K 2 Ca 2 (SO 4 ) 3 than 42 wt. per cent decompose with the formation of liquid and CaSO 4 .

Journal of Inorganic and Nuclear Chemistry

The solubility of quartz in water in the temperature interval from 25° to 300° C

The solubility of quartz in water was investigated by three sets of experiments at 1000 atm P H 2 O and temperatures ranging from 45° to 300°C at water pressures appropriate for the coexistence of three phases, gaseous water, liquid, and quartz, at temperatures ranging from 69° to 240°C a long term study of the dissolution of quartz grains which were continuously tumbled in water at room temperature. Saturated silica solutions in equilibrium with quartz were obtained in a few days at temperatures above 100°C. Equilibrium is shown by reproducible results for runs of different durations and by the precipitation of quartz from initially supersaturated solutions. The differential heat of solution derived from the data obtained at 1000 atm pressure is 5.38 kcal/mole. At room temperature and pressure, highly supersaturated silica solutions were obtained by continuously rotating quartz grains and water in plastic bottles at 75 rev/min. In one run the amount of silica in solution increased to a maximum value of 395 p.p.m. after 370 days. Another run reached 80 p.p.m. silica after 386 days and then dropped to 6 p.p.m. silica. It is concluded that quartz was precipitated at room temperature from this supersaturated solution and that 6 p.p.m. is essentially the true solubility of quartz at 25°C. In contrast to the runs rotated at 75 rev/min, quartz grains, and also silica glass grains, continuously rotated in water at rev/min, each contributed less than 1 p.p.m. colorimetric silica into solution after 1 year. Thus, vigorous agitation of the liquid is necessary to remove dissolved silica from the vicinity of surfaces of both quartz and glass. Two significant factors that may have contributed to the formation of supersaturated silica solutions in the runs rotated at 75 rev/min at room temperature are stresses and structural irregularities at the surfaces of the crushed quartz grains, which contributed silica into solution more readily than well crystallized quartz the very slow rate at which dissolved silica polymerizes to species appropriate to act as nuclei for quartz growth. At the termination of the runs rotated at 75 rev/min, spikelike projections were present on many of the quartz grains. These are interpreted as indicating that abrasion was not the dominant cause for the great supersaturations which were obtained.

Geochimica et Cosmochimica Acta