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排序方式: 共有206条查询结果,搜索用时 15 毫秒
81.
82.
Eric H. Oelkers Sergey V. Golubev Claire Chairat Oleg S. Pokrovsky Jacques Schott 《Geochimica et cosmochimica acta》2009,73(16):4617-6554
The surface chemistry of natural wollastonite, diopside, enstatite, forsterite, and albite in aqueous solutions was characterized using both electrokinetic techniques and surface titrations performed for 20 min in batch reactors. Titrations performed in such reactors allow determination of both proton consumption and metal release from the mineral surface as a function of pH. The compositions, based on aqueous solution analysis, of all investigated surfaces vary dramatically with solution pH. Ca and Mg are preferentially released from the surfaces of all investigated divalent metal silicates at pH less than ∼8.5-10 but preferentially retained relative to silica at higher pH. As such, the surfaces of these minerals are Si-rich and divalent metal poor except in strongly alkaline solutions. The preferential removal of divalent cations from these surfaces is coupled to proton consumption. The number of protons consumed by the preferential removal of each divalent cation is pH independent but depends on the identity of the mineral; ∼1.5 protons are consumed by the preferential removal of each Ca atom from wollastonite, ∼3 protons are consumed by the preferential removal of each Mg or Ca atom from diopside or enstatite, and ∼4 protons are consumed by the preferential removal of each Mg from forsterite. These observations are interpreted to stem from the creation of additional ‘internal’ adsorption sites by the preferential removal of divalent metal cations which can be coupled to the condensation of partially detached Si. Similarly, Na and Al are preferentially removed from the albite surface at 2 > pH > 11; mass balance calculations suggest that three protons are consumed by the preferential removal of each Al atom from this surface over this entire pH range. Electrokinetic measurements on fresh mineral powders yield an isoelectric point (pHIEP) 2.6, 4.4, 3.0, 4.5, and <1, for wollastonite, diopside, enstatite, forsterite, and albite, respectively, consistent with the predominance of SiO2 in the surface layer of all of these multi-oxide silicates at acidic pH. Taken together, these observations suggest fundamental differences between the surface chemistry of simple versus multi-oxide minerals including (1) a dependency of the number and identity of multi-oxide silicate surface sites on the aqueous solution composition, and (2) the dominant role of metal-proton exchange reactions on the reactivity of multi-oxide mineral surfaces including their dissolution rate variation with aqueous solution composition. 相似文献
83.
E.?S.?ZhitovaEmail author M.?P.?Popov S.?V.?Krivovichev A.?N.?Zaitsev N.?S.?Vlasenko 《Geology of Ore Deposits》2017,59(8):745-751
The paper describes the first finding of quintinite [Mg4Al2(OH)12][(CO3)(H2O)3] at the Mariinsky deposit in the Central Urals, Russia. The mineral occurs as white tabular crystals in cavities within altered gabbro in association with prehnite, calcite, and a chlorite-group mineral. Quintinite is the probable result of late hydrothermal alteration of primary mafic and ultramafic rocks hosting emerald-bearing glimmerite. According to electron microprobe data, the Mg: Al ratio is ~2: 1. IR spectroscopy has revealed hydroxyl and carbonate groups and H2O molecules in the mineral. According to single crystal XRD data, quintinite is monoclinic, space group C2/m, a =5.233(1), b = 9.051(2), c = 7.711(2) Å, β = 103.09(3)°, V = 355.7(2) Å3. Based on structure refinement, the polytype of quintinite should be denoted as 1M. This is the third approved occurrence of quintinite-1M in the world after the Kovdor complex and Bazhenovsky chrysotile–asbestos deposit. 相似文献
84.
Sabine Roedelsperger Michael Kuhn Oleg Makarynskyy Carl Gerstenecker 《Pure and Applied Geophysics》2008,165(6):1131-1151
It is sometimes assumed that steric sea-level variations do not produce a gravity signal as no net mass change, thus no change
of ocean bottom pressure is associated with it. Analyzing the output of two CO2 emission scenarios over a period of 2000 years in terms of steric sea-level changes, we try to quantify the gravitational
effect of steric sea-level variations. The first scenario, computed with version 2.6 of the Earth System Climate Model developed
at the University of Victoria, Canada (UVic ESCM), is implemented with a linear CO2 increase of 1% of the initial concentration of 365 ppm and shows a globally averaged steric effect of 5.2 m after 2000 years.
In the second scenario, computed with UVic ESCM version 2.7, the CO2 concentration increases quasi-exponentially to a level of 3011 ppm and is hold fixed afterwards. The corresponding globally
averaged steric effect in the first 2000 years is 2.3 m. We show, due to the (vertical) redistribution of ocean water masses
(expansion or contraction), the steric effect results also in a small change in the Earth’s gravity field compared to usually
larger changes associated with net mass changes. Maximum effects for computation points located on the initial ocean surface
can be found in scenario 1, with the effect on gravitational attraction and potential ranging from 0.0 to −0.7·10−5 m s−2 and −3·10−3 to 6·10−3 m2 s−2, respectively. As expected, the effect is not zero but negligible for practical applications. 相似文献
85.
86.
Alexey A. Krylov Oleg M. Khlystov Akihiro Hachikubo Hirotsugu Minami Yutaka Nunokawa Hitoshi Shoji Tamara I. Zemskaya Lieven Naudts Tatyana V. Pogodaeva Masato Kida Gennady V. Kalmychkov Jeffrey Poort 《Geo-Marine Letters》2010,30(3-4):427-437
We report on the isotopic composition of dissolved inorganic carbon (DIC) in pore-water samples recovered by gravity coring from near-bottom sediments at gas hydrate-bearing mud volcanoes/gas flares (Malenky, Peschanka, Peschanka 2, Goloustnoe, and Irkutsk) in the Southern Basin of Lake Baikal. The δ13C values of DIC become heavier with increasing subbottom depth, and vary between ?9.5 and +21.4‰ PDB. Enrichment of DIC in 13C indicates active methane generation in anaerobic environments near the lake bottom. These data confirm our previous assumption that crystallization of carbonates (siderites) in subsurface sediments is a result of methane generation. Types of methanogenesis (microbial methyl-type fermentation versus CO2-reduction) were revealed by determining the offset of δ13C between dissolved CH4 and CO2, and also by using δ13C and δD values of dissolved methane present in the pore waters. Results show that both mechanisms are most likely responsible for methane generation at the investigated locations. 相似文献
87.
This study is devoted to the numerical simulation of the artificial ground freezing process in a fluid-saturated rock mass of the potassium salt deposit. A coupled model of nonstationary thermal conductivity, filtration and thermo-poroelasticity, which takes into account dependence of the physical properties on temperature and pressure, is proposed on the basis of the accepted hypotheses. The considered area is a cylinder with a depth of 256 meters and diameter of 26.5 meters and includes 13 layers with different thermophysical and filtration properties. Numerical simulation was carried out by the finite-element method. It has been shown that substantial ice wall formation occurs non-uniformly along the layers. This can be connected with geometry of the freezing wells and with difference in physical properties. The average width of the ice wall in each layer was calculated. It was demonstrated that two toroidal convective cells induced by thermogravitational convection were created from the very beginning of the freezing process. The effect of the constant seepage flow on the ice wall formation was investigated. It was shown that the presence of the slow flow lead to the delay in ice wall closure. In case of the flow with a velocity of more than 30 mm per day, closure of the ice wall was not observed at all in the foreseeable time. 相似文献
88.
89.